B12-B1-Evolve-A1.txt Graham L. Kendall Modified 8/30/2008 Email grahamkendall74135@yahoo.com I am found on IRC Efnet/Undernet/Dalnet as glk Files on science and religion are found at http://www.grahamkendall.net/ All are free to use any of this material without limit. Linking to this url is allowed. ******************************************************************************* === Armored' fish study helps strengthen Darwin's natural selection theory by PhysOrg 'Armored' fish study helps strengthen Darwin's natural selection theory Shedding some genetically induced excess baggage may have helped a tiny fish thrive in freshwater and outsize its marine ancestors, according to a UBC study published today in Science Express. Measuring three to 10 centimetres long, stickleback fish originated in the ocean but began populating freshwater lakes and streams following the last ice age. Over the past 20,000 years - a relatively short time span in evolutionary terms - freshwater sticklebacks have lost their bony lateral plates, or "armour," in these new environments. "Scientists have identified a mutant form of a gene, or allele, that prohibits the growth of armour," says UBC Zoology PhD candidate Rowan Barrett. Found in fewer than one per cent of marine sticklebacks, this allele is very common in freshwater populations. Barrett and co-authors UBC post-doctoral fellow Sean Rogers and Prof. Dolph Schluter set out to investigate whether the armour gene may have helped sticklebacks "invade" freshwater environments. They relocated 200 marine sticklebacks with the rare armour reduction allele to freshwater experimental ponds. "By documenting the physical traits and genetic makeup of the offspring produced by these marine sticklebacks in freshwater, we were able to track how natural selection operates on this gene," says Rogers. "We found a significant increase in the frequency of this allele in their offspring, evidence that natural selection favours reduced armour in freshwater," says Barrett. Barrett and Rogers also found that offspring carrying the allele are significantly larger in size. "It leads us to believe that the genetic expression is also tied to increased growth rate," says Barrett. "If the fish aren't expending resources growing bones - which may be significantly more difficult in freshwater due to its lack of ions - they can devote more energy to increasing biomass," says Barrett. "This in turn allows them to breed earlier and improves over-winter survival rate." Celebrating its 150th anniversary this week, Darwin's first publication of his natural selection theory proposed that challenging environments would lead to a struggle for existence, or "survival of the fittest." Since then, scientists have advanced the theory by contributing an understanding of how genes affect evolution. "This study provides further evidence for Darwin's theory of natural selection by showing that environmental conditions can directly impact genes controlling physical traits that affect the survival of species," says Barrett. == Within the Order Cetecea, whales are divided into two sub-orders: the Odonteceti (toothed whales), which includes sperm whales, killer whales and dolphins, all of which eat fish and flesh; and the Mysticeti (baleen whales), which live by filtering plankton through a hairy sieve-like substance called baleen, these include blue whales, humpback whales and right whales. The difference in feeding habits might lead one to theorise an entirely separate ancestry for the two groups, but in fact studies have shown that all whales are descended from a common ancestor. The nature of this ancestor has been the subject of great debate and speculation, because of the amazing adaptations of these mammals to life in the water. Introduction: Modern Whales Before we begin, we should look briefly at the nature of modern whales. As stated, whales are mammals, a fact betrayed by their warm-blooded circulatory system, by the small hairs that can be found on their bodies, by the fact that they give birth to live young, not to eggs, and by the fact that they inhale air into their lungs rather than filter oxygen through gills. Collectively, all whales and dolphins are known as the order Cetecea. Modern whales are splendidly adapted to a permanent life in the sea. Their unique ears enable them to hear perfectly underwater. They have no legs, moving instead with flippers and the flukes of their huge tails. They do not have nostrils, having instead a single blowhole on top of their heads, which allows them to breathe while mostly submerged. They are able to give birth underwater, instead of coming onto the land like seals. The Odonteceti can use ultrasound to hunt, while all whales communicate with a complex language of 'songs' that carry for miles underwater. Within the Order Cetecea, whales are divided into two sub-orders: the Odonteceti (toothed whales), which includes sperm whales, killer whales and dolphins, all of which eat fish and flesh; and the Mysticeti (baleen whales), which live by filtering plankton through a hairy sieve-like substance called baleen, these include blue whales, humpback whales and right whales. The difference in feeding habits might lead one to theorise an entirely separate ancestry for the two groups, but in fact studies have shown that all whales are descended from a common ancestor. The nature of this ancestor has been the subject of great debate and speculation, because of the amazing adaptations of these mammals to life in the water. Why Leave the Land? Although the transformation from land animal to sea creature may seem extraordinary, the origins of such an occurrence may be observed among some communities of sheep that live on the coast of Scotland. These wild, goat-like sheep have lived on the coast for hundreds of years, and like to eat seaweed and kelp. They like seaweed so much that they are often observed swimming out into shallow waters to find it. Perhaps if we returned in ten million years, the descendants of these sheep would be seal-like or even whale-like creatures. And if herbivorous creatures are prepared to brave the seas for food, it would be even more attractive for those that were able to eat fish. However, while such theories are easy to hypothesise, proof has been lacking, and for a long time the fossil evidence for early whales was virtually non-existent. The First Finds The first fossil evidence for early whales arrived with the 1840 discovery in Egypt of Basilosaurus, an enormous, 40-million-year-old creature with a long, serpentine body, which was very whale-like in appearance, but also had tiny, useless hind legs indicative of a land-based origin. However, the discovery of Basilosaurus did not help greatly with the major questions of whale ancestry, since the creatures were so similar to modern whales that it remained difficult to imagine what their land-based ancestors were like. More intriguing evidence for the land-based ancestors of whales arrived with the discovery of the Mesonychids, an extinct type of mammal that flourished between 60 and 30 million years ago. Mesonychids were ungulates (hoofed animals), but unlike all other known ungulates they were meat-eaters. Many of them, including the terrifying Andrewsarchus, looked like wolves with hooves. Their most important feature, for our purposes, was their unusual, triangular teeth. The only other animals that have teeth similar to these are whales. For this reason, scientists long believed that whales must have evolved from a form of Mesonychid. Better evidence, however, remained elusive, and it was still difficult to imagine a transitional form between a Mesonychid and the whale-like Basilosaurus. A further suggestion was made by scientists studying DNA rather than fossils. They found that whale DNA was more similar to that of the Hippopotamids than any other living animal, and some subtle physical similarities between whales and hippos have also been noted. Could the origins of whales and hippos be linked? All of these suggestions have been clarified, and considerably altered, by a number of recent discoveries in Pakistan and India, which not only tell us more about the earliest whales, but also question the Mesonychid theory. Let us now look at the 'proto-whales' in chronological order. Pakicetids The earliest proto-whale that has been discovered is now Pakicetus, one of a group of creatures labelled the Pakicetids which lived around 52 million years ago. Pakicetus was about the size of a wolf. It looked nothing like a whale, and more like a cross between a large dog and a rat, having a long, thick tail. Despite this, many features of its skeleton link Pakicetus more closely to whales than to any other family. In particular, its ears, though not as sophisticated as those of modern whales, show the beginnings of this adaptation to underwater hearing. It is not known exactly how the Pakicetids lived, but they may have roamed the seashore, or hunted in rivers. The discovery of Pakicetus demonstrated the falsity of the Mesonychid theory; although the teeth indicate a shared ancestry, the skeletons of Pakicetus demonstrate that whales did not derive directly from Mesonychids. Instead, they are a form of Artiodactyl (another type of ungulate) which began to take to the water after the Artiodactyl family split from the Mesonychids. Thus, Pakicetids are early Artiodactyls that retain aspects of their Mesonychid ancestry which modern Artiodactyls have since lost. The Pakicetid fossils also helped to clarify the relationship of whales and hippos. It now seems that they are not very close relatives, except in that both are Artiodactyls. The likeliest explanation for the physical and genetic similarities is that hippos split off from the main Artiodactyl branch shortly after the whales did, and thus, like whales, retain some characteristics of early Artiodactyls. Both hippos and whales are Artiodactyls that became adapted to life in the water, but they did so separately and evolved in quite different directions. Ambulocetids While Pakicetus was clearly a land animal with minor adaptations to life in the water, this is less true of the recently discovered Ambulocetus, a 50 million-year-old skeleton of which was recently unearthed in Pakistan. The three-metre long Ambulocetus was an alarming animal that looked like a mammalian crocodile, having a long snout filled with teeth. It was amphibious - its back legs are better adapted for swimming than walking on land - and it probably swam by undulating its back vertically, as otters, seals and whales do. Like Pakicetus, Ambulocetus had developed an early form of the specialised ears possessed by modern whales, but there was still no blowhole. It is not certain whether these animals lived in rivers, the sea, or both. It has been suggested that Ambulocetids hunted like crocodiles, lurking in the shallows to snatch unsuspecting prey. Remingtonocetids The Remingtonocetid family were smaller cousins of the Ambulocetids, and lived at a similar time. They had longer snouts than those of Ambulocetus, and were slightly better adapted for underwater life. They probably lived similarly to modern sea otters, hunting for fish in the shallows. Protocetids The Protocetids were better-adapted for the water and lived around 45 million years ago. The best-known is Rhodocetus. The major Protocetid adaptation was the appearance of flukes (horizontal bars) on their tails, which enabled faster swimming. However, the skeletons of Rhodocetus indicate that they retained substantial hind legs. They lived in shallow seas, and may have had a similar lifestyle to seals, or even dolphins; it is not clear whether they ever came onto the land. Basilosaurus and Dorudon These new discoveries make it possible to understand how the descendants of creatures like these could look like Basilosaurus1. Basilosaurids lived around 38 million years ago and retained tiny, useless back legs. They were monsters, up to 18m long. Meanwhile, Dorudontids, which lived at the same time, were dolphin-sized, about 5m long. Although they look very much like modern whales, Basilosaurids and Dorudontids lacked the 'melon organ' that allows their descendants to sing and use ultrasound. They also had small brains, which suggests that they were solitary and didn't have the complex social structure of modern whales. Summary The transition from hoofed carnivore to sea leviathan is now understood in more detail than was possible even ten years ago. Pakicetids evolved into whales in a remarkably short time - about eight million years. However, these amazing transformations can now be observed in the fossil evidence of creatures that represent intermediate stages in the process. Gaps in our knowledge still remain - in particular the evolution of the blowhole remains mysterious - but hopefully further discoveries will provide answers to these questions. == The Antiquity of Man Similarities between apes and humans, and the implications for human evolution by Mikey Brass The anatomical evidence - both fossil and contemporary - demonstrates that australopithecines and chimpanzees share a geologically recent common ancestor and that Homo sapiens are descendants of the evolutionary branch that began with the divergence of the australopiths. The anatomical characteristics that link the australopiths to Homo, and show their intermediate form between modern humans and the last common ancestor between humans and chimpanzees, include: * The canines of the australopiths do not project much further forward in relation to the other teeth than they do in Homo; * Australopith canines also show a decrease in sexual size differences over time - the more recent forms are more like the condition of modern humans; * Tooth enamel progresses to a more Homo-like thickness over time; * Wear patterns on australopith teeth suggest a "crushing" action, similar to that of Homo; * The cranial capacity of the australopiths increases to a capacity range approaching that of early Homo; * The australopith foramen magnum, which allows the spinal cord to connect with the base of the brain, is located more toward the base of the skull than in apes, yet not completely under the skull, as in Homo but excluding the robust australopiths (also known as Paranthropus) where it was just as in Homo; and * The features of the tibiae (orientation angle, thickness and internal structure) shared by australopiths and Homo reflect the demands placed on their bodies by bipedalism. The anatomical similarities between chimpanzees and anatomically modern humans (Homo sapiens) can be summarized as follows: * In both species, the rib cage is broad from side to side and shallow from front to back; the rib cage extends back beyond the vertebral column * Both have a dorsally-placed scapula and shoulder joints facing outward to the side, giving humans a mobile shoulder joint; a hangover from our arboreal ancestry; and * The positioning and angle of the humeral shaft and humeral head and other joints in the forelimb are the same in both species. Table 1 below summaries the similarities and differences between chimpanzees, australopiths and modern humans as a result of millions of years of evolution. Modern chimpanzees Australopiths Modern humans Canines larger and project out from tooth row Canines slightly larger, but non-projecting Canines of similar size to other teeth and non-projecting Extended canine size determined by sexual dimorphism Moderate canine size determined by sexual dimorphism Minimal canine size determined by sexual dimorphism Thin tooth enamel Moderate tooth enamel Thick tooth enamel Dental wear pattern shows grinding action Dental wear pattern shows crushing action Dental wear pattern shows crushing action Cranial capacity average 400 cc Cranial capacity 350 - 540 cc Cranial Capacity > 1000 cc Foramen magnum opens toward rear of skull Foramen magnum opens between rear and base of skull Foramen magnum opens at base of skull Tibiae thin and angled Tibiae thicker and straighter Tibiae thick and straight Rib cage broad and extends past vertebral column Rib cage broad and extends past vertebral column Rib cage broad and extends past vertebral column Scapulae on the back, shoulder joints oriented to the sides Scapulae on the back, shoulder joints oriented to the sides Scapulae on the back, shoulder joints oriented to the sides It is also worthwhile noting Bernard Wood and Brian Richmond's (2000) summary of comparative limb morphology: "The substantial differences between the lower limbs of modern humans and apes are largely attributable to the bipedal locomotion of the former. The most striking difference is the great absolute and relative length of modern human lower limbs that increases stride length and thus the speed of bipedal walking. Because the lower limbs support the body during bipedal gait, the acetabulum, femoral head and other lower limb joints are relatively larger in humans. Modern human femora are distinctive in that they show the valgus condition (i.e. they converge towards the knees), thus helping to position the feet closer to the midline." In addition, recent reviews of the available anatomical (Shoshani et al. 1996) and genetic evidence (Ruvolo 1995, 1997; Wise et al. 1997) have convincingly re-affirmed yet again the theory that apes and anatomically modern humans share a common ancestry. The DNA sequences of human chromosomes 2 and 4 have been completely analysed and were published in the April 7 (2005) issue of Nature, reinforcing the conclusions reached by previous studies. In essence, the chimp chromosomes 2a and 2b fused to form the human chromosome 2. Previous comparisons between the chimpanzee and human genomes and other known genomes have yielded a gene which appears to be functional only in chimpanzees and humans. This gene is suggested to make a protein in the brain and testicals. Furthermore, , geneticists have analysed the differences in the amino acid sequences of protein and in the base sequences of DNA from apes and humans; the results have yielded a divergence time-frame of 5-8 million years ago. A good case study is that of the Dikika child, first published in 2006 and found by the Dikika Research Project members in Ethiopia. The sandstone sediment in which the child was found was deposited on a subaerial delta plain; the age of the Sidi Hakoma Member ranges from 3.31 - 3.35 million years. When combined with the lack of pre-weathering of the anatomical remains, these factors indicate that the child was buried in a flood. The initial anatomical report (Alemseged et al. 2006) is the accumulation of five years of painstaking cleaning and examination. Most of the postcranial remains were covered by sandstone matrix, together with the cranium's midface, left temporal bone and the cranial base. Analysis of the skeletal elements places the child firmly within the known range for Australopithecus afarensis and distinguish them from modern gorillas and chimpanzees. CT-scans were used to model the age using an African ape model. The resulting 3 years of age would not differ by more than a year and a half if a modern human model had been used instead. Given that A. afarensis is a hominin, the utilisation of an African ape model is a prudent measure for a minimum age. The tibiae has a sharper anterior border and its muscle attachment orientations resemble that of modern humans'. In addition, also like modern humans, the side of the upper part of the shaft is a little concave, becoming convex towards the back. The ape-like scapula, the longer phalanges and the reconstructed environmental settings (woodland with a nearby plain) all combine to reinvigorate investigations into the mobility patterns of A. afarensis. The basis of these investigations will likely be that A. afarensis combined a form of arboreal behaviour with habitual bipedalism, as reflected by the more derived lower body which would have been under heavy selection pressures. As more of the sandstone matrix is removed from the skeletal remains and further analysis is made possible (hopefully including isotope analysis), expect to see the new models of hominin growth, dietary and evolutionary patterns emerging over the coming years. These will yield valuable insights which can then be tested against the known and future anatomical remains of both A. afarensis and other hominin species. These models and predictions are based upon detailed anatomical evidence and do not use any particular religious text either as the starting point or as the given conclusion. Those who back such fundamentalist works display a profound ignorance of basic 1st year scientific methods, which places a huge question mark over the reliability of their own published and presented works. Creationist works, and those who support such efforts, have no basis whatsoever in any scientific procedure and basic plain scientific reality. References Alemseged, Z., Spoor, F. Kimbel, W., Bobe, R., Geraads, D., Reed, D. & Wynn, J. 2006. A juvenile early hominin skeleton from Dikika, Ethiopia. Nature 443(21): 296-301 Jungers, W.L. 1988. Relative joint size and hominoid locomotor adaptations with implications for the evolution of hominid bipedalism. In, Strasser, E. & Dagosto, M. (eds.) The Primate Postcranial skeleton: Studies in Adaptation and Evolution, pp. 247-265. London: Academic Press Pilbeam, D. 1996. Genetic and morphological records of the Hominoidea and hominid origins: a synthesis. Molecular Phylogenetics and Evolution 5: 155-168 Richmond, B. & Strait, D. 1999. Knuckle-walking traits retained in the wrists of early hominids. American Journal of Physical Anthropology, Suppl. 28: 232 Shoshani, J. et al. 1996. Primate phylogeny: morphological vs molecular results. Molecular Phylogenetic Evolution 5: 101-153 Tardieu, C. & Trinkaus, E. 1994. Early ontogeny of the human femoral bicondylar angle. American Journal of Physical Anthropology 95: 183-195 Walmsley, T. 1933. The vertical axes of the femur and their relations. A contribution to the study of erect posture. Journal of Anatomy 67: 284-300 Washburn, S.L. 1967. Behaviour and the origin of Man. Proceedings of the Royal Anthropological Institute 3: 21-27 Wise, C. et al. 1997. Comparative Nuclear and Mitochrondrial Genome Diversity in Humans and Chimpanzees. Molecular Biology Evolution 14(7): 707-716 Wood, B. & Richmond, B. 2000. Human evolution: taxonomy and paleobiology. Journal of Anatomy 196: 19-60 Wynn, J. Alemseged, Z., Bobe, R., Geraads, D., Reed, D. & Roman, D. 2006. Geological and palaeontological context of a Pliocene juvenile hominin at Dikika, Ethiopia. Nature 443(21): 332-336 == Perhaps the first and certainly the greatest example of an in-betweenie was Russian-born biologist Theodosius Dobzhansky. He showed what could be achieved when white coats were combined with wellingtons. Back in the 1930s, he began dusting down Darwinian evolution to leave it looking modern, shiny and new. In the early decades of the 20th century, with Darwin dead and Mendel on their minds, scientists were creating an entirely new way of looking at evolution. Instead of thinking about populations of plants and animals as collections of individuals, biologists like Dobzhansky began thinking exclusively in terms of genes and gene pools. As good as Darwin's evolutionary argument was, it had always lacked direct experimental evidence. By combining the fledgling science of genetics with Darwinian evolution, Dobzhansky gave Darwin's ideas the empirical kick up the backside they had been crying out for. But Dobzhansky's success was no solo affair. He would have got nowhere without his insect comrade, the fruit fly, Drosophila pseudoobscura. His choice of experimental organism may have seemed unusual. After all, Dobzhansky's tiny fruit flies were hardly a match for Darwin's finches, or so it seemed. But Dobzhansky chose wisely. By the 1930s, fruit flies had already proved themselves as pioneers in genetics research. They were cheap, prolific and easy to breed. They also had the biggest chromosomes that anyone had ever seen. Fruit flies, like footballers, produce immense quantities of saliva. The chromosomes inside the fruit fly's salivary glands are huge - a thousand times thicker than normal. Each chromosome is like a packet of spaghetti, made up of many parallel strands of DNA that have failed to separate. Chemical staining of these super-sized chromosomes reveals dark horizontal bands along their length, distinct landmarks corresponding to the positions of specific genes. When these chromosomes were first discovered in the 1930s, it was as revolutionary as the discovery of genetic fingerprints fifty years later. These super-sized chromosomes were like biological barcodes that gave biologists the first direct glimpse of genetic differences between individuals and populations. To Dobzhansky, the fruit fly chromosomes were a godsend and he spent years in the Californian wilderness collecting flies for analysis in the laboratory. His first discovery was that populations of flies living in different areas could be distinguished by the banding patterns of their chromosomes. In other words, populations were not genetically uniform, but differed from place to place. This may sound like common sense today and, even back then, it was what many biologists had suspected but it was the first time that anyone had provided the experimental proof. Yet more amazing was the discovery that these genetic differences were not static, but could change over remarkably short time scales. In the struggle for existence, natural selection favoured different chromosome types at different times of the year. These results were epoch-making for evolutionary biology. Because Darwinian natural selection had traditionally been considered a slow paced affair that was difficult - if not impossible - to test experimentally, critics had often dismissed the subject as unscientific. But here was a perfect demonstration of evolution in action. This was no million-year wait for a two millimetre increase in the length of a leg bone. This was evolutionary change in front of your very eyes. In accumulating genetic differences, Dobzhansky saw how two populations might also accumulate differences in body size, colour, genital architecture, behavioural idiosyncrasies, and a thousand other characteristics that could eventually make them reluctant or unable to mate with one another. In these distinct genetic profiles, Dobzhansky believed he was seeing the origin of species in its infancy. Dobzhansky had shown what was possible when scientists were willing to abandon their prejudices and break with tradition. His experiments with the fly brought about a sea change in evolutionary attitudes. Fruit fly genetics made evolution and the origin of species more credible to a once sceptical scientific community. Genetics not only tightened up Darwin's theory, it also turned evolutionary biology into a rigorous experimental science. Darwin would have given anything for a share of Dobzhansky's experimental spoils. Serves him right for looking at finches rather than flies. Fly: An Experimental Life, by Martin Brookes, is published by Weidenfeld & Nicholson, 16.99. == Whale barnacles are in the Coronulidae, which are highly specialized for life on living marine organisms.  Coronula is found at Calvert, but is a very low conic species, with 'hooks' on the base of the shell plates which embed the shell into the skin of the whale.  It is impossible to remove the barnacle from a living whale without cutting out a patch of skin.  More specialized Coronulidae embed completely into the skin, with only the aperture on the surface.  These species have no or very reduced shell plates, and would be difficult to recognize as fossils. == Miller, Stanley L., 1953 łA Production of Amino Acids Under Possible Primitive Earth Conditions˛ Science vol. 117:528-529 With a bit more information included in: Miller, Stanley, Harold C. Urey 1959 łOrganic Compound Synthesis on the Primitive Earth˛ Science vol 139 Num 3370: 254-251 == Acanthostega, had both lungs and gills. http://www.devoniantimes.org/ has transitionals == http://evolution.berkeley.edu/ http://www.natcenscied.org/article.asp http://www.ncseweb.org/resources/articles/7719_responses_to_jonathan_wells3_11_28_2001.asp == Birds release the fluke's eggs in their droppings, which are eaten by horn snails. The eggs hatch, and the resulting flukes castrate the snail and produce offspring, which come swimming out of their host and begin exploring the marsh for their next host, the California killifish. Latching onto the fish's gills, the flukes work their way through fine blood vessels to a nerve, which they crawl along to the brain They don't actually penetrate the killifish's brain but form a thin carpet on top of it, looking like a layer of caviar. There the parasites wait for the fish to be eaten by a shorebird. When the fish reaches the bird's stomach, the flukes break out of the fish's head and move into the bird's gut, stealing its food from within and sowing eggs in its droppings to be spread into marshes and ponds. == The name "colobus" is derived from the Greek word meaning "docked" or "mutilated." Colobus monkeys once were thought to be abnormal because they have no thumb, or only a small stub where the thumb would usually be. This is actually an adaptation rather than a mutilation which allows colobus monkeys to easily travel along the tops of branches quadripedally. == Researchers See History of Life in the Structure of Transfer RNA Transfer RNA is an ancient molecule, central to every task a cell performs and thus essential to all life. A new study from the University of Illinois indicates that it is also a great historian, preserving some of the earliest and most profound events of the evolutionary past in its structure. The study, co-written by Gustavo Caetano-Anolle s, a professor of crop sciences, and postdoctoral researcher Feng-Jie Sun, appears March 7 in PLoS Computational Biology. Caetano-Anolle s is an affiliate of the U. of I. Institute for Genomic Biology. Of the thousands of RNAs so far identified, transfer RNA (tRNA) is the most direct intermediary between genes and proteins. Like many other RNAs (ribonucleic acids), tRNA aids in translating genes into the chains of amino acids that make up proteins. With the help of a highly targeted enzyme, each tRNA molecule recognizes and latches onto a specific amino acid, which it carries into the protein- building machinery. In order to successfully add its amino acid to the end of a growing protein, tRNA must also accurately read a coded segment of messenger RNA, which gives instructions for the exact sequence of amino acids in the protein. The fact that tRNA is so central to the task of building proteins probably means that it has been around for a long time, Caetano- Anolles said. His inquiry began with a hunch that understanding the structural properties of tRNA would shed light on how organisms and viruses evolved. "Perhaps in evolution there are things that are so fundamental that they are kept, held onto, for millions or even billions of years," Caetano-Anolle s said. "Those are the fossils, the molecular fossils, that tell us about the past. Therefore, studying these molecules can address fundamental questions in biology and evolution." All tRNAs assemble themselves into a shape that, if flattened, resembles a cloverleaf. The team began by looking for patterns in this cloverleaf structure, using detailed data from hundreds of molecules representing viruses and each of the three superkingdoms of life: archaea, bacteria and eukarya. The researchers converted all distinguishing features of the individual tRNA cloverleaf structures into coded characters, a process that allowed a computerized search for the most "parsimonious" (that is, the simplest, most probable) tRNA family tree. They conducted the same analysis on the tRNAs of each of the superkingdoms, to see how far these groupings diverged from the overall tree. This comparison allowed them to determine the order in which viruses and each of the superkingdoms diverged. The new analysis supports an earlier study that suggested that the archaea were the first to arise as an evolutionarily distinguishable group. Archaea are microbes that can survive in boiling acid, near sulfurous ocean vents or in other extreme environments. The earlier study, also led by Caetano-Anolle s, analyzed the vast catalog of protein folds those precisely configured regions in proteins that give them their functionality as a guidebook to evolutionary history. "The transfer RNA data matches our earlier data," Caetano-Anolle s said. "This is important because two lines of independent evidence are supporting each other." The new analysis also indicates that viruses emerged not long after the archaea, with the superkingdoms eukarya and bacteria following much later and in that order. This finding may influence the ongoing debate over whether viruses existed prior to, or after, the emergence of living cells, Caetano-Anolle s said. "This supports the idea that viruses arose from the cellular domain," he said. == Examples of transitions in the fossil record In the '70s, creationist polemicist Gish predicted that proto-mammals with two jaw joints would never be found. Promptly thereafter, lots of them were from all around the world, despite the far from ideal conditions of their environments & small size for fossilization. (The older jaw joint became the mammalian inner ear bones, while the newer jaw joint is the one that creationists share with asses.) More recently, ID advocate Behe predicted that walking whales would never be found, but was just as promptly shown wrong. Evolution predicts transitional fossils, & they're found, while creationists' predictions are always shown false. == Inactivation of the EGF-TM7 receptor EMR4 after the Pan-Homo divergence We here report on the identification of a novel human EGF-TM7 receptor, designated EMR4. Like most EGF-TM7 receptor genes, EMR4 is localized on the short arm of chromosome19, in close proximity to EMR1. Remarkably, due to a one-nucleotide deletion in exon8, translation of human EMR4 would result in a truncated 232-amino acid protein lacking the entire seven-span transmembrane region. This deletion is not present in nonhuman primates, including chimpanzees, suggesting that EMR4 became nonfunctional only after human speciation, about five million years ago. Thus, EMR4 surprisingly accounts for a genetic difference between humans and primates related to immunity. == The centromere (middle connection) of human chromosome #2 is composed of the telomeres (end caps) of two smaller standard ape chromosomes, demonstrating an important genetic event in human evolution. Chromosome centromeres are also useful in tracing the surprisingly recent evolution of some species of genus Equus, ie horses, donkeys & zebras: http://www.ncbi. nlm.nih.gov/ pubmed/16413164 Single genus Equus shows about the same genetic distance among its species as do humans with our closest relatives, the great apes, despite humans, chimps (with bonobos), gorillas & orangs all having been awarded our own genera, Homo, Pan, Gorilla & Pongo. == Monkey DNA Points to Common Human Ancestor A rhesus macaque pictured at the Southwest National Primate Research Center. A female from the center provided the DNA sample used in the genome sequencing. Credit: Southwest National Primate Research Center at Southwest Foundation for Biomedical Research in San Antonio A rhesus macaque pictured at the NIH Animal Center in Poolesville, MD. Credit: Science/Joshua Moglia The first primate to get rocketed into space and to be cloned, the rhesus monkey, has now had its genome sequenced, promising to improve research into health and yield insights into human evolution. Analysis of the monkey's DNA sequence has also deepened a few mysteries in our understanding of the biology of primates when it comes to vital parts of our biology, such as the X chromosome. Rhesus macaques (Macaca mulatta) are sandy-furred, pink-faced monkeys that live in the region ranging from Afghanistan to northern India, as well as southern China, and are traditionally held as sacred in Hinduism. They have a long history as lab monkeys. For instance, the Rh factor in blood discovered in 1937, the presence or absence of which dubs a person's blood type either 'positive' or 'negative,' derives its name from rhesus monkeys. Even now, they are the animals of choice for research into drug addiction and HIV, and roughly two-thirds of all National Institutes of Health-funded primate-related studies use the monkeys. For example, the rhesus monkey Tetra, born in 2000, was the first cloned primate. 93 percent common DNA The sequence of the rhesus macaque's genome will be a powerful tool for research with the monkeys aimed at understanding human biology, said consortium leader Richard Gibbs, director of the Baylor College of Medicine's Human Genome Sequencing Center in Houston. "Right now if you perform an experiment on a person, there's no way that you would think that all people are the same, when it comes to a response to a drug or behavior or anything," Gibbs told LiveScience. Macaques have about the range of diversity when it comes to their genetics, "so being able to understand them on a genetic level will help explain variation in their responses and will allow for smarter experiments that make us more clever at deciphering results." The new analysis of the rhesus monkey genome, conducted by an international consortium of more than 170 scientists, also reveals that humans and the macaques share about 93 percent of their DNA. By comparison, humans and chimpanzees share about 98 to 99 percent of their DNA. The fact that rhesus monkeys are further away from humans in evolution will help illuminate what makes humans different from other apes in ways that chimps, which are so closely related to us, could not, Gibbs said. (Rhesus monkey ancestors diverged from those of humans roughly 25 million years ago, while chimpanzees diverged from our lineage 6 million years ago.) In addition, the researchers identified roughly 200 genes that appear to be key players "in defining the shapes of species, in what makes the primates different from us and each other," Gibbs said. These include genes involved in hair formation, sperm-egg fusion, immune response and cell membrane proteins, findings detailed in the April 13 issue of the journal Science. Unusual role of X chromosome The research also raised a few surprises. For instance, the monkey's X chromosome showed an unexpectedly large number of times in which its parts got shuffled around. This is consistent with the same mysterious rearrangements seen in the human lineage's X chromosome following the branching off of the chimpanzee, and gives "us new evidence of the unusual role of this sex chromosome in primate evolution," said researcher Aleks Milosavljevic at the Baylor College of Medicine. Another as yet unexplained phenomenon the sequencing revealed has to do with lumps of DNA known as centromeres, which hold together the two separate strands of DNA that make up a chromosome, acting somewhat like the center of an X. Strangely, nine of the 22 centromeres the monkeys have repositioned themselves on their chromosomes in the last 25 million years. As to why this happened, "no one knows," said researcher Mariano Rocchi at the University of Bari in Italy. The rhesus monkey genome sequence should prove invaluable to biomedical research, said physician scientist Ajit Varki at the University of California at San Diego, who participated in the chimpanzee genome sequencing project. "And if we can get the genome sequences of one representative from each primate lineage, we could reconstitute the ancestral primate genome--what the genome of our common ancestor some 40 to 50 million years ago looked like," he told LiveScience. "That would be an amazing feat." == Scientists found life in a 2-mile-deep mine in South Africa, that's the first case of discovering life that is completely independent of what happens on the surface. The microbes live off of gases from radioactive activity produced in the rock. == Native to Arizona, these whip tail lizards somehow managed to entirely eliminate the male of the species. As a result, the lizards are what scientists call "parthenogenetic unisexual pseudocopulators." Since there are no males, the females reproduce on their own, making exact copies of themselves. However, the lizards still need another woman to get the job done. A female, noted by her small undeveloped eggs, will hop on another female who has rich, robust, ready-to-be-fertilized eggs, and mock humps her. == Hormone governs caterpillar's bird dropping disguise A hormone is the secret behind the unusual ability of young swallowtail caterpillars to disguise themselves as bird droppings and then copies of the leaves they live on before becoming butterflies, Japanese researchers found. Writing on Thursday in the journal Science, the researchers said a special hormone -- juvenile hormone -- keeps larvae of the butterfly Papilio xuthus, which is commonly found in Japan, in their black and white bird-excrement camouflage. As they reach the last stage of caterpillar development, levels of this hormone drop, triggering a transformation into the green leaf phase.SEMEN "We found that juvenile hormone works as a switch for the camouflage pattern. That is a novel aspect of this hormone," Haruhiko Fujiwara of the National Institute of Agrobiological Sciences in Japan, who worked on the study, said in an e-mail. Juvenile hormones are known to regulate many aspects of insect development including molt -- when an insect sheds its outer shell -- and metamorphosis -- as when a caterpillar becomes a butterfly, he said. What Fujiwara and colleagues discovered, however, was that juvenile hormone also appears to govern this camouflage process. He said the hormone may regulate genes involved in color, pattern and surface formation. As for the bird-poop disguise, Fujiwara said it likely keeps the larvae safe from hungry birds until they are more mobile, but they did not study this. == What did the immediate ancestor of chimps and humans look like? Comparing living chimpanzees to living humans, in reference to the species that gave rise to these two closely related species, is one way to frame questions about the evolution of each species. Generally, it is useful to address evolutionary questions by comparing two living species with the reconstructed "last common ancestor" (LCA) of those species. All of the similarities and differences between the LCA and the living form, in each lineage, represent evolutionary "stories" (that could even be worked out as hypotheses). Similarities indicate important, long-maintained adaptations, and differences indicate evolutionary changes that are ripe for exploration. The different stories that go with each lineage may reflect historically important events, such as the effects of biogeography, climate change, or other changes in the ecology or behavior of the organisms. One argument that has emerged over the last several years, championed by David Pilbeam and Richard Wrangham, and used by Wrangham and me is our paper on Roots and the evolution of Australopithecus (and related species), is that the chimp-human LCS can be modeled as a chimp-like organism. This argument implies that chimps have not changed much since the chimp-human split, while most of the changes have been along the human lineage. One might think that this is a human-centric approach, but it is not. It is simply taking the available evidence for what it means and going with it. This argument is based on triangulation. Imagine a phylogeny (family tree) showing gorillas, chimps, bonobos, and humans. Based on the genetic evidence, it would look something like this: Using apes in general as a reference point, the gorilla-chimp ancestor is likely to have been a chimp-like form. Gorillas seem to have evolved from a chimp like ancestor, with a change in growth pattern to make gorillas both larger and more sexually dimorphic (dimorphic = "different shape") in body size, and to have derived features of their teeth. Again, using apes in general as a reference point, everything that seems to be different between bonobos and chimps seems most likely to be a derived feature added to bonobos. This suggests that the LCA of chimps and bonobos is more like a chimp than a bonobo. When we look at fossils of early human ancestors, from back near to the chimp-human split, we see mostly chimp-like features with a mix of derived (added on) features depending on which early hominid species we look at. Most of the differences in postcrania are minor (even given bipedalism) and most of the differences in the skull have to do with a single set of related changes in dentition that relate to a dietary shift. Again, we see chimp-ness. From the point of view of all of these reference points, the best model is that the chimp-human LCA is most like a chimp, and that gorillas, bonobos, early human ancestors, and of course humans, are all different from chimps in ways that reflect evolutionary novelties. The chimp, in other words, is the ultimate forest ape, so well adapted to its environment that is has changed very little. All the other species are either close derivations of this form, or more dramatic changes, each of these changes reflecting some environmental (or other) challenge that was, luckily, transformed into an adaptive shift (if you like adaptations), a random change (following relaxed selection?) or extinction. The living forms, obviously, have not yet undergone extinction. I remember asking a close friend of mine about the fossil record for the chimpanzee side of the split recently; she held up her hand in the shape of a 0. Perhaps there are a few scraps, but I really hope there's a more concerted effort to fill in the gaps on the chimpanzee side, especially since it would either support or refute some of what you've mentioned above. I agree that chimps, for the most part, are the best model we have for the LCA. That being said, even though I didn't agree with Aaron Filler's mechanism I am intrigued with his hypothesis that knuckle-walking is a derived trait and that the LCA might have been more gibbon-like in form (which goes back to Sir Arthur Keith). Unfortunately fossils of the lineage leading up to chimpanzees are going to be hard to find; if they remained in the forest taphonomy is against us, but I think it's still important to look. Coming up with some such remains would be a test of the modern chimpanzee as a model for the LCA and either support what was said here or cause us to revise our ideas. Perhaps the research isn't as "sexy" as searching for the earliest humans, but I think it's just as important to understanding our own evolution. == This suborder of burrowing squamates show vestigial, non-functional limb bones, eyes & ears. Except for the Mexican genus Bipes, which retains its forelimbs. All squamate groups present problems for creationists, of course, just as do all living things. But scaly "reptiles" are particularly tough. The evolution of snakes will be sorted out in coming years, as we find more Mesozoic fossils & derive more genomes, which have already helped resolve relationships among the worm lizards. I did not mean that snakes are polyphyletic but would not rule our paraphyletic. I am saying that venomosity (and, hence, its structures) is not a linearly evolved adaptation. Homologies between some venom proteins are the result of the genetic adaptation of normal physiological proteins...for example Cobra Venom Factor from the gene for C3,Bb..in a common ancestor. The glyphic structures may not, therefore, be evolved from each other such as aglyph->opisthoglyp h->proteroglyph- >solenoglyph. It is my view that some of the transitional squamata between Lacertilia and Serpentes were venomous and that some of the Mosasaurid-descende nt ancestors of snakes were venomous. There is a tendency to view venomosity as a recently evolved adaptation in the Reptilia but it was probably present in the Jurassic. I have a fossil sea snake, probably a macrostomate, from the Cretaceous but there is no way to determine if it was venomous. Extant Hydrophiids are probably "return to the sea" species unrelated to that fossil. The elongation of the supratemporals and quadrates and skull structure of macrostomates suggests they ate very large prey and, unlike recent terrestrial snakes, constriction was probably not an option with marine prey. A snake 1-2 meters long eating prey larger in circumference than itself, underwater, would be a perfect candidate for venomosity to avoid injury from struggling prey. The teeth os Eupodophis are very large for holding, much like a tree boa, but much thicker, further apart and the final maxillary tooth appears to be more elongated. This differs from Pachyrhachis where the dentition appears closer together and resembles that of a boid. I think it is possible that the placement of the venom apparati in living venomous snakes between colubroid and soleno/proteroglyph s may be convergent. == From genome to "venome": Molecular origin and evolution of the snake venom proteome inferred from phylogenetic analysis of toxin sequences and related body proteins ABSTRACT Top This study analyzed the origin and evolution of snake venom proteome by means of phylogenetic analysis of the amino acid sequences of the toxins and related nonvenom proteins. The snake toxins were shown to have arisen from recruitment events of genes from within the following protein families: acetylcholinesterase, ADAM (disintegrin/metalloproteinase), AVIT, complement C3, crotasin/ defensin, cystatin, endothelin, factor V, factor X, kallikrein, kunitz-type proteinase inhibitor, LYNX/SLUR, L-amino oxidase, lectin, natriuretic peptide, nerve growth factor, phospholipase A2, SPla/Ryanodine, vascular endothelial growth factor, and whey acidic protein/secretory leukoproteinase inhibitor. Toxin recruitment events were found to have occurred at least 24 times in the evolution of snake venom. Two of these toxin derivations (CRISP and kallikrein toxins) appear to have been actually the result of modifications of existing salivary proteins rather than gene recruitment events. One snake toxin type, the waglerin peptides from Tropidolaemus wagleri (Wagler's Viper), did not have a match with known proteins and may be derived from a uniquely reptilian peptide. All of the snake toxin types still possess the bioactivity of the ancestral proteins in at least some of the toxin isoforms. However, this study revealed that the toxin types, where the ancestral protein was extensively cysteine cross-linked, were the ones that flourished into functionally diverse, novel toxin multigene families. Venomous snakes possess one of the most sophisticated integrated weapons systems in the natural world. The advanced snakes (superfamily Colubroidea) make up >80% of the 2900 species of snake currently described, and contain all of the known venomous forms (Greene 1997; Vidal 2002). Snake venom glands evolved a single time, at the base of the colubroid radiation, 60-80 million years ago, with extensive subsequent "evolutionary tinkering" (Vidal and Hedges 2002; Fry and Wuster 2004). Evidence comes from comparative morphology, embryology, and developmental biology, as well as the demonstrated homology of venom-secreting glands of different colubroid families (Kochva 1963, 1965, 1978; Underwood and Kochva 1993; Underwood 1997; Jackson 2003), as well as the distribution of these glands across the full spectrum of "colubrid" families (Vidal 2002) in addition to phylogenetic analyses of toxin sequences (Fry et al. 2003a,b; Fry and Wuster 2004). As maxillary fangs and a venom gland are a colubroid synapomorphy, the distinction between the "Duvernoy's gland" and the atractaspidid/elapid/viperid venom glands has been abandoned (Fry et al. 2003c). It has been previously postulated that some of the snake toxin types (such as three-finger toxins) evolved from a single ribonuclease ancestor (Strydom 1973). It has also been hypothesized that the snake venom gland itself evolved in the mouth region as a consequence of an evolutionary change in the pancreatic trait, and consequently, some of the toxins should show strong affinities to pancreatic proteins (Kochva 1987). Therefore, a fundamental question that has remained unanswered is what gene types were recruited for use in the snake venom proteome and what were the tissue locations from which these genes were harvested? Another major remaining unanswered question is what biochemical characteristics do these ancestral proteins share? The purpose of this study was to use phylogenetic analyses of toxin and related body proteins to reconstruct the evolutionary history of snake venom proteome in order to provide a frame-work for use in answering these questions. Examined in this study were the following snake toxin types: 3FTx (three-finger toxin), acetylcholinesterase, ADAM (disintegrin/metalloproteinase), CVF/C3 (cobra venom factor/complement C3), crotamine, cystatin, factor V, factor X, kallikrein, kunitoxins, L-amino oxidase, lectins (C-type and galactose binding), MIT (mamba intestinal toxin), natriuretic peptide, NGF (nerve growth factor), PLA2 (phospholipase A2), sarafotoxin, SPRY (SPla/Ryanodine), VEGF (vascular endothelial growth factor), wagerlin, and waprin (Table 1). The conventionally recognized, major classes of a particular protein type, characterized by activity type and specific functional motifs, formed monophyletic groups. These groupings were congruent whether by Bayesian analysis (Figs. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11) or maximum parsimony (data not shown) and supported by high posterior probabilities. Of the 24 snake toxin types examined, 23 had matches with known protein types (Table 2). In 11 data sets (acetylcholinesterase, CNP-BPP, CRISP, CVF, crotamine, factor V, factor X, L-amino oxidase, type IB PLA2, and type IIA PLA2) the toxin sequences were nested within a nontoxin subclade, with high posterior probability support, thus allowing for clear inference of gene origin (Figs. 1, 2, 3, 4, 5). In seven data sets (ADAM, cystatin, MIT, kallikrein, lectin, sarafotoxin, and SPRY), the toxin sequences formed sister groups to body protein types with high bootstrap value support, allowing for inference of ancestral nontoxin gene, but definitive assignment to a particular subclade not being possible (Figs. 6, 7, 8, 9A). In five data sets (3FTx, BNP, kunitz type proteinase inhibitor, VEGF, and waprin), high levels of saturation, combined with short sequence length, produced polytomies that did not allow for assignment of the toxins to specific clade within the larger protein family (Figs. 1B, 9B, 10, 11). The waglerin toxins from Tropidolaemus wagleri (Wagler's Viper) (Aiken et al. 1992) did not have a match with any known protein types, and genome mining did not reveal any high confidence matches within protein-coding regions. Past hypotheses suggested that proteins of pancreatic origin should be the dominant snake toxins (Strydom 1973; Kochva 1987). However, the results of this study reveal a diverse array of tissues from which toxin encoding genes were harvested and the bioactivities equally diverse (Tables 3, 4). While there was no pattern with regard to specific tissue type, with many of the ancestral gene types expressed in several tissues, all coded for secretory proteins. Comparison of toxins and ancestral body proteins allowed for a determination of ancestral versus derived activities (Tables 5, 6). For example, the phylogenetic association of the 3FTx with the nicotinic acetylcholine receptor-binding LYNX and SLUR peptides (e.g., Miwa et al. 1999; Ibanez-Tallon et al. 2002; Chimienti et al. 2003) is consistent with the basal -neurotoxic activity of the 3FTx (Fry et al. 2003a). This is in contrast to previous hypotheses of an ancestral digestive action for this toxin type (Strydom 1973). Significant changes in the gene structure have not been currently documented for the snake toxins relative to their protein ancestors, with the exception of the sarafotoxins and the ADAM toxins. The gene structure of sarafotoxins is quite distinct from that of the ancestral endothelin peptides, being arranged in a rosary, with several coding regions in tandem (Ducancel et al. 1993). In a highly derived form of the ADAM toxins (e.g., Q6T6T2 from Bitis gabonica), the regions upstream of the C-terminal disintegrin domain have been excised, and the transcripts code now solely for the disintegrin domain. The selection pressure resulting in this change is indicative of the usefulness of this domain to the snake in prey capture. Currently, the gene location for only one toxin type (crotamine) has been determined, with the transcripts located at the chromosomal tips (Radis-Baptista et al. 2003). The chromosomal location of the endogenous ancestor crotasin (Q6HAA2) is unknown. Molecular scaffold characteristics Extensive cysteine cross-linking was revealed to be a beneficial characteristic of proteins recruited for use as toxins (Table 7). Such proteins were more likely to have come from multigene families, as well as the toxin subgroup flourishing into a new multigene family with extensive functional diversification. This bias is due to the stability of the molecular core, and thus, these proteins are amenable to extensive functional diversification. Supporting this trend, the toxin types that have been independently recruited for use in other animal venoms are also extensively cysteine cross-linked (Table 7). However, the apparent bias toward mutations in the toxins of residues at the tips of loops (Fry et al. 2003b) and lower rate of mutations of the cysteines and flanking residues (which have structural, rather than functional roles), may, in fact, be an arti-fact. Intracellular housekeeping enzymes are more likely to proteolytically destroy proteins that have had a mutation of a key structural residue, such as cysteine or a flanking amino acid. This may be a consequence of such changes, potentially resulting in the protein being unable to form stable tertiary conformations. Transcriptome studies may reveal more mRNA transcripts with mutations in key structural residues than in proteins secreted as part of the "venome." A similar force may be at work to produce the apparent strong correlation between extensive cysteine connectivity and the tendency for formation of functionally diverse multigene families (Table 7). This may be due to the beneficial stability of an extensively cysteine-linked molecular scaffold in comparison to the much more loosely constructed tertiary structure of globular proteins formed by noncovalent interactions. For such globular proteins, a single amino acid change may be enough to decimate the ability of the protein to fold into a stable conformation, and unstable proteins are once again more likely to be destroyed by intracellular housekeeping enzymes. Thus, mutations that may have enabled functional diversification in globular proteins may have also produced fatal structural changes. Similarly, cDNA/EST studies may yet again reveal more mutations in mRNA transcripts coding for globular proteins than in secreted protein libraries. In this study, the BNP and CNP-BPP natriuretic peptides had a high amino acid:cysteine ratio (Table 7). The very long preproregion of the natriuretic peptides includes a number of noncysteine-linked small peptides (e.g., cardiodilatin-related peptides) that are cleaved off upstream of the circulating form of the natriuretic peptide itself. The final highly processed form of the natriuretic peptides contains the only two cysteines coded for by the full gene, which form the 17 amino acid loop essential for the GC-A/GC-B receptor binding activity (Bovy 1990). The molecular evolution of the factor X blood proteins also appeared at first glance to be contrary to the pattern displayed by other data sets. The factor X blood proteins are highly structurally and functionally conserved in the body, despite being extensively cysteine cross-linked (Table 7). However, this is a likely consequence of negative selection pressure against variations in such a crucial aspect of hemostasis, with mutations likely to have catastrophic effects resulting in embryonic mortality. No newly evolved activities have been documented for the factor X toxins, possibly due to their recent recruitment in the Australian elapid snake lineage and existing extremely potent and useful action. However, multiple isoforms exist in each of the venoms containing this toxin type. This is indicative of these toxins evolving via the birth-and-death model, as has been previously shown for the 3FTx (Fry et al. 2003b). As a result, the factor X toxins may ultimately acquire novel activities. Potential salivary origin of two of the snake toxin types Two of the toxin types present in the snake venome, CRISP and kallikrein, may not actually have been the result of gene recruitment events, but rather modifications of secreted proteins already present in the ancestral salivary tissue that gave rise to the venom gland. Both are phylogenetically extremely close to toxins from the venomous lizards in the Heloderma genus (Beaded Lizards and Gila Monsters) such as Q91055 [GenBank] (helothermine) and P43685 [GenBank] (gilatoxin), respectively (Figs. 2A, 8A). The shared toxins between the snake and Helodermatid lizard venoms represent independent recruitments of proteins for use as toxins, as the venom-secreting structures in advanced snakes and Heloderma lizards are different, nonhomologous structures (glands located in the supralabial and infralabial regions, respectively), and the last common ancestor of Heloderma and advanced snakes would have been a basal varanoid (Forstner et al. 1995; Lee 1997) or even a basal scleroglossan (Rieppel et al. 2003) lizard devoid of a venomous function. In addition to the close phylogenetic relationships revealed in this study, helothermine and gilatoxin have biochemical actions similar to the ancestral activities of the snake venom equivalents. The snake CRISP toxins induce hypothermia, possibly mediated through their demonstrated relaxation of the peripheral smooth muscle through blockage of K+-induced contraction, potentially by acting upon voltage-gated Ca2+ channels (Yamazaki et al. 2002). Helothermine from the venomous lizard Heloderma horridum (Beaded Lizard) has been reported to have a myriad of activities, including blocking of voltage-gated Ca2+ channels, K+ channels and ryanodine receptors, as well as introduction of hypothermia (Mochca-Morales et al. 1990; Nobile et al. 1994, 1996; Morrissette et al. 1995). The isolation of toxins with the same action (relaxation of smooth muscle and induction of hypothermia) from divergent groups of snakes, as well as the unrelated venomous lizards, indicates that this may be the original activity of the common protein ancestor. Similarly, both the snake and lizard kallikrein toxins are sister groups to the mammalian tissue (glandular) kallikrein, secreted in a wide variety of tissues including saliva glands (Fig. 8A). Gilatoxin also displays significant similarity of action to the snake venom equivalents, releasing bradykinin from kininogen with subsequent lowering of blood pressure (Utaisincharoen et al. 1993). Clearly, in either case, the snake and lizard toxins were recruited from closely related body proteins, reflective of the wide-spread presence of CRISP and kallikrein proteins in salivary tissue and other exocrine tissue. In light of the strong phylogenetic associations, the similarity of bioactivities and the relationship to known salivary proteins, the most parsimonious explanation is that both toxin types are derivations of previously existing salivary proteins. Sequencing and phylogenetic analysis of both protein types from nontoxin-secreting salivary tissue from venomous and nonvenomous lizards and snakes would be revealing in this context. Presence of snake toxin types in other animal venoms In addition to the presence of CRISP and kallikrein in lizard venoms, other protein types have been independently selected for use as toxins by other venomous animals. Disparate members of the protein superfamily to which the CRISP proteins belong are used in venoms of cone snails, such as Q7YT83 from Conus textile (Cloth-of-gold cone snail) and insects, such as P10736 [GenBank] from Dolichovespula maculata (White-face hornet) and P35778 [GenBank] from Solenopsis invicta (Fire ant). However, the activities of these toxins differ considerably from the reptilian CRISP toxins. The toxin from Conus textile has a proteinase activity, while the insect toxins are the major venom allergens. Interestingly, CRISP-related proteins are also the major allergens in insect saliva, such as Q9NH66 from Ctenocephalides felis (Cat flea), Q7Z0B5 from Stomoxys calcitrans (Stable fly), and Q8T9U1 from Aedes aegypti (Yellowfever mosquito). Intriguingly, CRISP-related proteins are also utilized by plants for defence against fungi (e.g., PR-1 protein P35792 [GenBank] from Hordeum vulgare [Barley]), and other proteins are the hallmark of certain cancer types (e.g., the glioma pathogenesis-related protein P48060 [GenBank] ). None of these other CRISP-related proteins align near the snake or lizard venom toxins (Fig. 2A). The PLA2 proteins have also been recruited on numerous occasions, ranging from Q7M4I5 from Apis dorsata (Giant honeybee), Q8WS88 from Adamsia carciniopados (Cloak Sea Anemone), and P80003 [GenBank] from Heloderma suspectum (Gila Monster) venoms, with a wide variety of evolved activities. It is notable that the PLA2 from Heloderma venoms are not biochemically or phylogenetically related to either of the snake PLA2 toxin types, reinforcing the uniqueness of the relationships of the CRISP and kallikrein toxins. Intriguingly, the kunitz peptides in sea anemone venom have been convergently evolved for the same unique K+ channel-blocking activity as the highly derived Dendroaspis (Mamba) venoms within the Elapidae snake family (Schweitz et al. 1994, 1995). Ornithorhynchus anatinus (Platypus) venom contains high amounts of CNP natriuretic toxins (e.g., de Plater et al. 1998a,b), but of a form that lacks the derived BPP domains found in the snake brain and venom peptides. Two snake toxin types have been independently recruited for use in amphibian toxic skin secretions. The AVIT peptides on frog skin have a similar toxic action as the snake MIT toxins, causing intestinal cramping and increased sensitivity to pain (Mollay et al. 1999). AVIT-like peptides have also been reported from spider venoms (Szeto et al. 2000), but other than sharing the cysteine arrangement, the arachnid toxins lack all of the invariant residues, as well as the contractive effect upon smooth muscle and the ability to produce hyperalgesia. Toxins related to the snake venom 3FTx are secreted on the skin of Xenopus laevis (African clawed frog) (e.g., Q09022 [GenBank] ). These toxins are phylogenetically and functionally distinct from the snake venom 3FTx, acting presynaptically by activating dihydropyridine-sensitive Ca2+ channels (Kolbe et al. 1993). These toxins appear to be wide-spread in amphibians, with related peptides (e.g., Q71TU4) having been sequenced from the skin of Plethodon jordani (Jordan's salamander). Notably, all of the above shared toxin types are extensively cysteine cross-linked, come from functionally diverse multigene families, and all have been developed into toxin multigene families (Table 7). The multiple, independent recruitment of certain protein types for use as toxins also sheds additional light on what sorts of proteins are favored in molecular evolution and what sort of molecular scaffold is beneficial. However, unlike the Heloderma CRISP and kallikrein toxins, they are all phylogenetically very distinct from the snake equivalents. This reinforces the uniqueness of the close relationship between the snake and lizard CRISP and kallikrein toxins and the most parsimonious explanation of these two toxin types arising from modification of existing salivary proteins. Conclusion The results of this study suggest that the tissue types from which the toxin recruitment genes were selected were as diverse as the proteins themselves. Two toxin types (CRISP and kallikrein) actually appear to be modifications of proteins already present in the ancestral salivary tissue. While the activity of the ancestral protein has been invariably retained, toxin types originating from extensively cysteine cross-linked proteins have been the ones to flourish into newly derived, functionally diverse, toxin multigene families. In order to minimize confusion, all proteins' sequences are referred to by their SWISS-PROT accession numbers (http://www.expasy.org/cgi-bin/sprot-search-ful). Sequences were obtained through BLAST searching using representative toxin sequences (http://www.expasy.org/tools/blast/). Resultant sequence sets were aligned using the program CLUSTAL-X (Thompson et al. 1997), followed by visual inspection for errors. In the cases where peptides have been incorporated as domains into longer preproteins (Kunitz protease inhibitors, whey acidic protein, and SPRY), alignments were trimmed on either side of the domain. Due to the large number of sequences in each data set, phylogenetic analyses were conducted in two steps. For each data set, phylogenetic trees containing all sequenced proteins were initially reconstructed using the maximum parsimony (MP) method, conducted using the program PAUP*4.0b10 (Swofford 2002) and random stepwise taxon addition with TBR branch swapping and the PROTPARS weighting scheme (Felsenstein 2001), which takes into account the number of changes required at the nucleotide level to substitute one amino acid for another. Number of sequences, alignment length (including gaps), and parsimony informative sites are shown in Table 1. In this manner, clades that contained the venom proteins were identified. Once such clades were identified, data sets containing representative venom proteins, all the nearest neighbor nonvenom sequences, and representatives of the full breadth of gene phylogenetic diversity were selected and then analyzed using Bayesian inference implemented on MrBayes, version 3.0b4 (Huelsenbeck and Ronquist 2001; Ronquist and Huelsenbeck 2003). The method uses Markov-chain Monte Carlo methods to generate posterior probabilities for each clade represented in the tree. The analysis was performed by running a minimum of 1*106 generations in four chains, and saving every 100th tree. The log-likelihood score of each saved tree was plotted against the number of generations to establish the point at which the log likelihood scores of the analysis reached their asymptote, and the posterior probabilities for clades established by constructing a majority rule consensus tree for all trees generated after the completion of the burn-in phase. Sequence alignments and unrooted maximum parsimony trees can be obtained by e-mailing Dr. Bryan Grieg Fry Aiken, S.P., Sellin, L.C., Schmidt, J.J., Weinstein, S.A., and McArdle, J.J. 1992. A novel peptide toxin from Trimeresurus wagleri acts pre- and post-synaptically to block transmission at the rat neuromuscular junction. Pharmacol. Toxicol. 70: 459-462.[Medline] Bovy, P.R. 1990. Structure activity in the atrial natriuretic peptide (ANP) family. Med. Res. Rev. 10: 115-142.[CrossRef][Medline] Chimienti, F., Hogg, R.C., Plantard, L., Lehmann, C., Brakch, N., Fischer, J., Huber, M., Bertrand, D., and Hohl, D. 2003. Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda. Hum. Mol. Genet. 12: 3017-3024.[Abstract/FreeFullText] de Plater, G.M., Martin, R.L., and Milburn, P.J. 1998a. The natriuretic peptide (ovCNP-39) from platypus (Ornithorhynchus anatinus) venom relaxes the isolated rat uterus and promotes oedema and mast cell histamine release. Toxicon 36: 847-857.[Medline] ____. 1998b. A C-type natriuretic peptide from the venom of the platypus (Ornithorhynchus anatinus):structure and pharmacology. Comp. Biochem. Physiol. C Pharmacol. Toxicol. Endocrinol. 120: 99-110.[CrossRef][Medline] Ducancel, F., Matre, V., Dupont, C., Lajeunesse, E., Wollberg, Z., Bdolah, A., Kochva, E., Boulain, J.C., and Menez, A. 1993. Cloning and sequence analysis of cDNAs encoding precursors of sarafotoxins. Evidence for an unusual "rosary-type" organization. J. Biol. Chem. 268: 3052-3055.[Abstract/FreeFullText] Felsenstein, J. 2001. PHYLIP (Phylogeny Inference Package) version 3.6. Department of Genetics, University of Washington, Seattle, WA. http://evolutiongeneticswashingtonedu/phyliphtml. Forstner, M.R.J., Davis, S.K., and Arevalo, E. 1995. Support for the hypothesis of anguimorph ancestry for the suborder Serpentes from phylogenetic analysis of mitochondrial DNA sequences. Mol. Phylogenet. Evol. 4: 93-102.[CrossRef][Medline] Fry, B.G. and Wuster, W. 2004. Assembling an arsenal: Origin and evolution of the snake venom proteome inferred from phylogenetic analysis of toxin sequences. Mol. Biol. Evol. 21: 870-883.[Abstract/FreeFullText] Fry, B.G., Lumsden, N.G., Wuster, W., Wickramaratna, J.C., Hodgson, W.C., and Kini, R.M. 2003a. Isolation of a neurotoxin (-colubritoxin) from a nonvenomous colubrid: Evidence for early origin of venom in snakes. J. Mol. Evol. 57: 446-452.[CrossRef][Medline] Fry, B.G., Wuster, W., Kini, R.M., Brusic, V., Khan, A., Venkataraman, D., and Rooney, A.P. 2003b. Molecular evolution and phylogeny of elapid snake venom three-finger toxins. J. Mol. Evol. 57: 110-129.[CrossRef][Medline] Fry, B.G., Wuster, W., Ramjan, S.F.R., Jackson, T., Martelli, P., and Kini, R.M. 2003c. Analysis of Colubroidea snake venoms by liquid chromatography with mass spectrometry: Evolutionary and toxinological implications. Rapid Commun. Mass Spectrom 17: 2047-2062.[CrossRef][Medline] Greene, H.W. 1997. Snakes: The evolution of mystery in nature. Univertsity of California Press, Berkeley, CA. Huelsenbeck, J.P. and Ronquist, F. 2001. MrBayesBayesian inference of phylogeny, Version 30b4 Bioinformatics 17: 754-755.[Abstract/FreeFullText] Ibanez-Tallon, I., Miwa, J.M., Wang, H.L., Adams, N.C., Crabtree, G.W., Sine, S.M., and Heintz, N. 2002. Novel modulation of neuronal nicotinic acetylcholine receptors by association with the endogenous prototoxin lynx1. Neuron 33: 893-903.[CrossRef][Medline] Jackson, K. 2003. The evolution of venom-delivery systems in snakes. Zool. J. Linn. Soc. 137: 337-354.[CrossRef] Kochva, E. 1963. Development of the venom gland and trigeminal muscles in Vipera palaestinae. Acta Anatomica 52: 49-89. ____. 1965. The development of the venom gland in the opisthoglyph snake Telescopus fallax with remarks on Thamnophis sirtalis (Colubridae, Reptilia). Copeia 147-154. ____. 1978. Oral glands of the Reptilia. In: Biology of the Reptilia, (eds. C.K. Gans and A. Gans), Vol. 8, pp. 43-162. Physiology B Academic Press, UK. Kochva, E. 1987. The origin of snakes and evolution of the venom apparatus. Toxicon 25: 65-106.[Medline] Kolbe, H.V., Huber, A., Cordier, P., Rasmussen, U.B., Bouchon, B., Jaquinod, M., Vlasak, R., Delot, E.C., and Kreil, G. 1993. Xenoxins, a family of peptides from dorsal gland secretion of Xenopus laevis related to snake venom cytotoxins and neurotoxins. J. Biol. Chem. 268: 16458-16464.[Abstract/FreeFullText] Lee, M.S.Y. 1997. The phylogeny of varanoid lizards and the affinities of snakes. Phil. Trans. Roy. Soc. London Ser. B-Biol. Sci. 352: 53-91.[CrossRef] Miwa, J.M., Ibanez-Tallon, I., Crabtree, G.W., Sanchez, R., Sali, A., Role, L.W., and Heintz, N. 1999. lynx1, an endogenous toxin-like modulator of nicotinic acetylcholine receptors in the mammalian CNS. Neuron 23: 105-114.[CrossRef][Medline] Mochca-Morales, J., Martin, B.M., and Possani, L.D. 1990. Isolation and characterization of helothermine, a novel toxin from Heloderma horridum horridum (Mexican beaded lizard) venom. Toxicon 28: 299-309.[Medline] Mollay, C., Wechselberger, C., Mignogna, G., Negri, L., Melchiorri, P., Barra, D., and Kreil, G. 1999. Bv8, a small protein from frog skin and its homologue from snake venom induce hyperalgesia in rats. Eur. J. Pharmacol. 374: 189-196.[CrossRef][Medline] Morrissette, J., Kratzschmar, J., Haendler, B., el-Hayek, R., Mochca-Morales, J., Martin, B.M., Patel, J.R., Moss, R.L., Schleuning, W.D., Coronado, R., et al. 1995. Primary structure and properties of helothermine, a peptide toxin that blocks ryanodine receptors. Biophys. J. 68: 2280-2288.[Abstract/FreeFullText] Nobile, M., Magnelli, V., Lagostena, L., Mochca-Morales, J., Possani, L.D., and Prestipino, G. 1994. The toxin helothermine affects potassium currents in newborn rat cerebellar granule cells. J. Membr. Biol. 139: 49-55.[Medline] Nobile, M., Noceti, F., Prestipino, G., and Possani, L.D. 1996. Helothermine, a lizard venom toxin, inhibits calcium current in cerebellar granules. Exp. Brain Res. 110: 15-20.[Medline] Radis-Baptista, G., Kubo, T., Oguiura, N., Svartman, M., Almeidae, T.M.B., Batistic, R.F., Oliveira, E.B., Vianna-Morgante, A.M., and Yamane, T. 2003. Structure and chromosomal localization of the gene for crotamine, a toxin from the South American rattlesnake, Crotalus durissus terrificus Toxicon 42: 747-752. Rieppel, O., Zaher, H., Tchernov, E., and Polcyn, M.J. 2003. The anatomy and relationships of Haasiophis terrasanctus, a fossil snake with well-developed hind limbs from the Mid-Cretaceous of the Middle East. J. Paleont. 77: 536-558.[Abstract/FreeFullText] Ronquist, F. and Huelsenbeck, J.P. 2003. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19: 1572-1574.[Abstract/FreeFullText] Schweitz, H., Heurteaux, C., Bois, P., Moinier, D., Romey, G., and Lazdunski, M. 1994. Calcicludine, a venom peptide of the Kunitz-type protease inhibitor family, is a potent blocker of high-threshold Ca2+ channels with a high affinity for L-type channels in cerebellar granule neurons. Proc. Natl. Acad. Sci. 91: 878-882.[Abstract/FreeFullText] Schweitz, H., Bruhn, T., Guillemare, E., Moinier, D., Lancelin, J.M., Beress, L., and Lazdunski, M. 1995. Kalicludines and kaliseptine. Two different classes of sea anemone toxins for voltage sensitive K+ channels. J. Biol. Chem. 270: 25121-25126.[Abstract/FreeFullText] Strydom, D.J. 1973. Snake venom toxins: The evolution of some of the toxins found in snake venoms. Syst. Zool. 22: 596-608.[CrossRef] Swofford, D.L. 2002. PAUP*Phylogenetic analysis using parsimony *and other methods beta version 40b10. Sinauer Associates, Sunderland, MA. Szeto, T.H., Wang, X.H., Smith, R., Connor, M., Christie, M.J., Nicholson, G.M., and King, G.F. 2000. Isolation of a funnel-web spider polypeptide with homology to mamba intestinal toxin 1 and the embryonic head inducer Dickkopf-1. Toxicon 38: 429-442.[Medline] Thompson, J.D., Gibson, T.J., Plewniak, F., Jeanmougin, F., and Higgins, D.G. 1997. The CLUSTAL_X windows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 25: 4876-4882.[Abstract/FreeFullText] Underwood, G. 1997. An overview of venomous snake evolution. In Venomous snakes: Ecology, evolution and snakebite (eds. R.S. Thorpe, W.Wuster, and A. Malhotra), pp. 1-13, Symposia of the Zoological Society of London, No 70, Clarendon Press, Oxford, UK. Underwood, G. and Kochva, E. 1993. On the affinities of the burrowing asps Atractaspis (Serpentes: Atractaspididae). Zool. J. Linn. Soc. 107: 3-64. Utalsincharoen, P., Mackessy, S.P., Miller, R.A., and Tu, A.T. 1993. Complete primary structure and biochemical properties of gilatoxin, a serine protease with kallikrein-like and angiotensin-degrading activities. J. Biol. Chem. 268: 21975-21983.[Abstract/FreeFullText] Vidal, N. 2002. Colubroid systematics: Evidence for an early appearance of the venom apparatus followed by extensive evolutionary tinkering. J. Toxicol. Toxin Rev. 21: 21-41. Vidal, N. and Hedges, S.B. 2002. Higher-level relationships of caenophidian snakes inferred from four nuclear and mitochondrial genes. C.R. Biol. 325: 987-995. Yamazaki, Y., Koike, H., Sugiyama, Y., Motoyoshi, K., Wada, T., Hishinuma, S., Mita, M., and Morita, T. 2002. Cloning and characterization of novel snake venom proteins that block smooth muscle contraction. Eur. J. Biochem. 269: 2708-2715.[Medline] B. G. Fry, H. Scheib, L. van der Weerd, B. Young, J. McNaughtan, S. F. R. Ramjan, N. Vidal, R. E. Poelmann, and J. A. Norman Evolution of an Arsenal: Structural and Functional Diversification of the Venom System in the Advanced Snakes (Caenophidia) Mol. Cell. Proteomics, February1,2008; 7(2): 215 - 246. [Abstract] [Full Text] [PDF] == Evolution is descent with modification. Random changes in the genetic makeup of an organism result in changes in the phenotype. The organism interacts with its environment. If the changes to the phenotype give it an advantage over others - the vast majority of genetic changes are deleterious -- it leaves more offspring, who are also endowed with this advantageous genetic makeup for dealing with their environment. This latter is known as "natural selection." This simple but powerful process leads to new species through separation of organisms in time and place. == THREE years before his death in 1805, English philosopher William Paley proposed a now-famous thought experiment. Imagine discovering a watch on the heath: how would you explain its intricate arrangement of parts, its clear design for a purpose? Naturally, you'd conclude that it was built by a watchmaker, not blown together by chance. By analogy, Paley argued, the natural world is full of designed complexity which must therefore also have a creator: God. Had Paley been in a position to know about it, he would no doubt have considered a remarkable little device called the bacterial flagellum to be an excellent example of designed complexity. With its intricate arrangement of interconnecting parts, the flagellum looks no less designed than a watch, and would surely have had Paley reaching for the existence of its "maker". Modern biology, of course, has no need for omniscient designers. Evolution - Richard Dawkins's blind watchmaker ... == Bats flew before they had 'radar' NEW YORK A fossil found in Wyoming has apparently resolved a long-standing question about when bats gained their radar-like ability to navigate and locate airborne insects at night. The answer: after they started flying. The discovery revealed the most primitive bat known, from a previously unrecognized species that lived some 25.5 million years ago. Its skeleton shows it could fly, but that it lacked a series of bony features associated with "echolocation," the ability to emit high-pitched sounds and then hear them bounce back from objects and prey, researchers said. Until now, all the early known fossil bats showed evidence of both flying and echolocating, so they couldn't reveal which ability came first, said researcher Nancy Simmons. Her team's research appears in Thursday's issue of the journal Nature. Simmons chairs the vertebrate zoology division at the American Museum of Natural History in New York. The early bat's wingspan was nearly a foot, just a bit smaller than that of today's big brown bat, she said. Its teeth show it ate insects, which it evidently plucked off surfaces after seeing, smelling or hearing them, she said. Simmons said she suspects the bat was active at night, but she noted there's no evidence for that. The creature was unusual for having a claw on all five fingers rather than just one or two. Researchers dubbed it "Onychonycteridae finneyi," meaning "clawed bat." The name honors Bonnie Finney, the commercial collector who found the fossil in 2003. Two specimens of the creature have been recovered. "These outstanding fossils considerably advance our understanding of bat evolution," researcher John Speakman of the University of Aberdeen in Scotland wrote in a Nature commentary. == An example is the Zebra Longwing butterfly, which feeds on only one small group of closely related plants. They genetically recognize these plants, probably by their chemical odors, and lay their eggs solely on these. == A fossil of a new crab species reveals the itsy-bitsy crustaceans inhabited towering sponge reefs during the Jurassic Period, where they made tasty snacks for ichthyosaurs and other ancient reptiles. The fossil was discovered in eastern Romania within cylindrical reef structures about 100 feet (30 meters) across and just as tall, which were once blanketed by deep ocean. It represents a new species within the oldest lineage of true crabs that lived 150 million years ago when dinosaurs walked the Earth. Dubbed Cycloprosopon dobrogea, the primitive crab was built for sidling in and out of crevices in reefs, with a flattened body just under a half-inch (6 millimeters) long. Exactly how the crab moved about, however, is not known, as this species and other family members had no legs extending from the carapace, or outer body covering. "They probably were hiding in the small cracks and crevices within the sponge reef itself," said lead researcher Carrie Schweitzer, a geologist at Kent State University in Ohio. The underwater hideouts would've proved critical to survival in the face of ancient reptiles nosing around for tasty morsels. "These crabs in the Jurassic were living in much deeper water than a dinosaur would've been, but something like an ichthyosaur or a plesiosaur would certainly have been eating crabs," Schweitzer told LiveScience. Schweitzer has uncovered other Jurassic crabs in this area and elsewhere, indicating, she says, that the crustaceans were much more diverse and plentiful than scientists had thought. == Evolution describes an active response to the environment but it is passive. Because variation exists within a species, the environment both biotic and abiotic decide the shape of an organism. The forces in the world are not random. It is wetter on the coast, dryer in the interior, colder towards the poles, hotter towards the equator. If you took a zoo and emptied half its contents into an equatorial rainforest and the other half on the arctic tundra, you would quickly see how the environment will select those that have the necessary structure and behavior to survive. Putting something in mathematical terms does not make it correct. Any work must ultimately be reviewed by other scientists with necessary background. It is not a perfect system but it is a lot better than teaching as science anything that enters the public fancy. == Origin of Vision Discovered You are reading these words right now because 600 million years ago, an aquatic animal called a Hydra developed light-receptive genesthe origin of animal vision. It wasn't exactly 20-20 vision back then though. Hydras, a genus of freshwater animals that are kin to corals and jellyfish, measure only a few millimeters in diameter and have been around for hundreds of millions of years. Scientists at the University of California, Santa Barbara studied the genes associated with vision (called opsins) in these tiny creatures and found opsin proteins all over their bodies. Though they don't have eyes or any specific light-receptive organs, researchers think that the light-sensing proteins concentrated in the mouth area of the Hydras help them to use light sensitivity to search out prey. Because studies of animals that evolved earlier, such as sponges, don't show the same light sensitivity, scientists were able to pinpoint the Precambrian date that animal vision first started to evolve. "We now have a time frame for the evolution of animal light sensitivity," said study leader David Plachetzki, a UC Santa Barbara graduate student. "We know its precursors existed roughly 600 million years ago. These findings, detailed in a recent issue of the online journal PLoS ONE, counter arguments by anti-evolutionists that evolution can only eliminate traits and cannot produce new features, the authors say. Our paper shows that such claims are simply wrong," said co-author Todd Oakley, also a UC Santa Barbara biologist. "We show very clearly that specific mutational changes in a particular duplicated gene (opsin) allowed the new genes to interact with different proteins in new ways. Today, these different interactions underlie the genetic machinery of vision, which is different in various animal groups. == Origin of Apes Humans are great apes and are one of the species in the family Hominidae along with only a few other species. The Hominidae include two distinct species of the genus Pan: Pan paniscus (bonobos) and Pan troglodytes (chimpanzees), two species of gorillas (Gorilla gorilla and Gorilla graueri), and two species of orangutans (Pongo pygmaeus and Pongo abelii). Apes in turn belong to the Primates order (>375 species). Data from both mitochondrial and nuclear DNA indicates that primates belong to the group of Euarchontoglires, together with Rodentia, Lagomorpha, Dermoptera, and Scandentia.[1] This is further supported by Alu-like SINEs which have been found only in members of the Euarchontoglires. === Evolution is the process by which survivors will adapt to changed circumstances, or go extinct. == Both eutherian cats and metatherians have evolved saber-toothed species. the saber-toothed marsupials had oversized incisors and the saber-toothed cat's saber teeth were canines. A pair of big sharp teeth seems to be the only commonality, and that characteristic only emerges because the theria, as a group, had differentiated teeth. When you take a Cretaceous era predator which also fed on prey much larger than itself, you see something like Velociraptor, which had a enlarged claw, rather than saber teeth, because the teeth of Velociraptor were not very differentiated. Here again, different evolutionary trajectories produce different solutions to the same problem. === Some exquisitely fine studies of microanatomy suggests the brain of amphioxus has regions equivalent to the tripartite division seen in the vertebrates. == http://fm1.fieldmuseum.org/aa/Files/patterso/Dick___Patterson_2006_MicromammalsMacroparasites.pdf bat flies == Ruse. LIFE'S SOLUTION Steven Johnson's 'Emergence: The Connected Lives of Ants, Brains, Cities, and Software.' Wesson "Beyond Natural Selection" Ryan "Dawin's Blindspot" Simon Conway Morris "Life's Solutions" The Emergence of Everything: How the World Became Complex (Paperback) by Harold J. Morowitz (Author) == Piltdown Man claim was made by Mr. Charles Dawson at Piltdown, Sussex, between the years 1911 and 1915. He "found" the greater part of the left half of a deeply mineralized human skull, also part of the right half; the right half of the lower jaw, damaged at certain parts but carrying the first and second molar teeth and the socket of the third molar or wisdom tooth. After much controversy, it turned out to be not a primitive man at all, but a composite of a skull of modern man and the jawbone of an ape. ... The jawbone had been 'doctored' with bichromate of potash and iron to make it look mineralized." === The Counter-Creationism Handbook by Mark Isaak Michel Onfray In Defence of Atheism All the changes to human evolutionary thought should not be considered a weakness in the theory of evolution, Kimbel said. Rather, those are the predictable results of getting more evidence, asking smarter questions and forming better theories, he said. == ORIGINS: A Skeptic's Guide to the Creation of Life, by Robert Shapiro, === ------------------------------------------------------------------------ How Giant Dinosaurs Survived Vulnerable Youth Titanosaurs were among the largest creatures to ever walk the Earth, with some gargantuan examples believed to have weighed more than 100 tons. Bony scales dotted their hides, but their purpose remained a mystery. Analysis of titanosaur embryos suggest these scales helped protect the giants during their vulnerable youth, guarding them against predators. Paleontologist Thiago Marinho at the Federal University of Rio de Janeiro analyzed data on titanosaur eggs discovered in Patagonia in Argentina in 1997. The embryos within had evidence of skin that bore a number of bumps. Comparison with skin patches seen in alligator embryos suggested the dinosaur bumps might one day toughen up into bony scales known as osteoderms. The osteoderms seen on adult titanosaurs were too small and spongy to provide much real defense. Marinho noted such body armor would have been far more effective for young titanosaurs than adults, protecting against the bites of marauders such as theropodscarnivorous dinosaurs that included T. rexas well as crocodile-like predators known as crocodyliforms. Such armor would have proven especially helpful for young titanosaurs, since no fossil evidence exists that titanosaurs displayed much in the way of parental care, Marinho added. "Although the titanosaurs comprise some of the biggest land animals to walk on Earth, we have to keep in mind that they were born from eggs 30 centimeters [12 inches] in diameter," Marinho said. While such eggs might be huge by modern standards, the 1-foot-long or so hatchlings resulting from them "wouldn't stand a chance against big theropod dinosaurs. But they might have had an effective defense system against small theropods and terrestrial crocodyliforms if they had a cuirass [protective covering] composed by side-by-side osteoderms." Marinho figures that as titanosaurs grew, they absorbed as much calcium as they could to form their massive skeletons, including from their osteoderms, making these bony scales more porous and spongy. "Extant crocodilians, especially juveniles and young adults, do absorb calcium from their osteoderms when their diets do not supply the calcium demand for their metabolism," he explained. As the dinosaurs grew older, the bony scales "would have become obsolete accessories, as the size of the titanosaurs was itself a defense system." Other dinosaurs were known to have possessed bony scales as well, such as the predatory theropod Carnotaurus. While scant fossil evidence of young or embryonic theropod skin has been found as yet, the notion that juvenile theropods might have had bony scales to protect them"can't be discarded," Marinho said. == "Hypercycles and the origin of life" nature, vol 280 pp445-46. reprinted in Maynard Smith 1982, pp34-38 == http://www.fieldmuseum.org/ Great long == David Sloan Wilson. Evolution can also be applied to almost every aspect of human life, as he demonstrates in his first book for a general audience, Evolution for Everyone: How Darwin's Theory Can Change the Way We Think About Our Lives (Bantam Press 2007). == Rev Sun Myung Moon paid for Wells to get a college degree so he would have some "authority" when criticizing evolution. == In a 1999 interview with Insight Magazine, Johnson explained why he singled out evolution when his real target was all of modern science: "Evolution is a creation story and as a creation story, it's the main prop of the materialist explanation for our existence." == In the physical sciences, abiogenesis, the question of the origin of life, is the study of how life on Earth might have emerged from non-life sometime between 4.4 billion years ago, when liquid water first flowed on the Earth, and 2.7 billion years ago when the earliest uncontroversial evidence of life is found in the form of stable isotopes[1][4] and molecular biomarkers pointing to photosynthesis. == A list" of endangered species, however, lists 784 species driven to extinction since 1500--ranging from the dodo bird of Mauritius to the golden toad of Costa Rica. == Since you claim to have heard of fossils, are you aware that the sequence of fossils found pretty much anywhere on Earth looks like this (thanks to Matt): first bacteria below first multicellular organism below first shelled organisms below first insects below first amphibians below first reptiles below first dinosaurs below first birds below first placental mammals below first apes below first hominids Evolution has an explanation for this. Creationism does not. == http://www.milleran dlevine.com/ km/evol/DI/ clot/Clotting. html == Discovery of new species of fish gives evolution clues BEIJING, May 7 (Xinhua) -- A Chinese research team has discovered four fossils of a new species of fish dating back 400 million years which may provide clues to the evolution of fish. Dr. Zhu Min, the leading scientist from the Chinese Academy of Sciences (CAS) Institute of Vertebrate Paleontology and Pale anthropology, said Sunday that the newly discovered species may represent a bridge between two vertebrate lineages that ultimately went on to dominate the modern world. The find made by Zhu and his colleagues was published in the latest issue of the British journal Nature. The fossilized creature, found in southwest China's Yunnan Province, combines features shown by ray-finned bony fishes, including the majority of modern fish species, and by lobe-finned bony fishes, the group that spawned the ancestors of today's land vertebrates, Dr. Zhu said. The ancient fish, represented by chunks from four separate skulls, has a skull roof much like that of actinopterygian, the group that includes most modern fish, Dr. Zhu said. But the fine features of its anatomy may also shed light on the evolutionary origin of cosmine - a hard surface-tissue found in many fossil sarcopterygians, the fish that later gave rise to land vertebrates, he said. Cosmine is characterized by a network of pores and canals in the tissue, overlaid by a single enamel-based layer, Zhu explained. The 405 million-year-old fossil possessed several such layers over the pore-canal network, suggesting that the cosmine arose after all but one of these layers disappeared, he said. Zhu named the ancient fish after his mentor, Prof. Meemann Chang, China's most prominent paleontologist and also a CAS member. Prof. Chang laid the foundation of modern research on ancient bony fishes. With the latest find, Dr. Zhu and his team are trying to prove that lobe-finned bony fishes originated from south China. == 160,000-Year-Old Child Suggests Modern Humans Got Early Start Bucking conventional wisdom, a new study says early members of our species, Homo sapiens, may have known what it was like to be a kid. A long childhood is considered one of things that separate so-called modern humans from the first Homo sapiens and older human species, such as Homo erectus. Now a study of a 160,000-year-old early Homo sapiens child found in North Africa may change how earlyand wherewe think modern humans arose. A Study With Teeth European researchers used x-ray imaging to study the growth patterns of teeth in the juvenile fossil found in Morocco. Similar to tree rings, the patterns are a record of aging. What they revealed is that this fossil is the earliest known human with a long childhood, according to Tanya Smith, an anthropologist at the Max Planck Institute for Evolutionary Anthropology in Germany. In the teeth the scientists found signs of modern-human development patternsthat is, relatively long periods of slow development and growth. A prolonged childhood is seen as necessary for the type of learning that leads to culture and complex society. The juvenile fossil "showed an equivalent degree of tooth development to living [modern] human children at the same age," the report authors write. According to the researchers, the study challenges theories about when and where humans acquired modern bodies and behaviors. The findings also may help prove that "modern biological, behavioral, and cultural characteristics" were relative latecomers in the past six million years of human evolution. "These findings are in contrast to studies that suggest that earlier fossil hominins [humans and our ancestral species] possessed short growth periods, which were more similar to chimpanzees than to living humans," the study authors write in this week's issue of the journal Proceedings of the National Academy of Sciences. Study co-author Smith said her research team knew that human ancestors living several million years ago grew up differently from modern children. "What we didn't know was when the modern human condition of a long childhood and slow period of growth and development evolved," she said. The study suggests that developmentally modern humans existed at least 160,000 years ago, which Smith says is just slightly younger than the earliest fossil Homo sapiens from East Africa. Promising New Method "It is a great result that today we can really measure growth rates of teeth due to CT [and] x-ray technology," said Professor Ottmar Kullmer, a paleoanthropologist at the Research Institute Senckenberg in Germany. "These new possibilities of modern analysis methods augment the understanding of early Homo sapiens development and human evolution in general." Kullmer, who was not a participant in the study, said that the discovery of a relatively long human childhood about 160,000 years ago points to "a complex social system in early Homo sapiens groups." "Probably, social behavior was one of the important survival strategies of early humans." == Learn the controversy: sympatric versus allopatric speciation When one looks carefully at a biological problem, one can usually discover more than one casual explanationIndeed, it is quite possible that in biology the majority of phenomena and processes must be explained by a plurality of theories. Ernst Mayr This is Biology (1997) One long standing controversy in evolutionary biology is about the respective contributions sympatry and allopatry have made during the origins of the millions of species that now exist. A new species (or 2 new species) can develop if gene flow between 2 populations ceases or slows down to permit the independent evolution of the 2 populations. Allopatric (or geographic) speciation takes place when 2 populations are geographically isolated from each other by, for example, a mountain chain, or an ocean. Because the members of the 2 populations cannot mate and exchange genes with each other, the populations may start to diverge genetically and phenotypically and eventually end up being 2 separate species. In extreme cases of allopatry, there will be no gene flow between the diverging populations. The opposite of this is sympatric speciation, which takes place in 2 populations whose distribution ranges are largely overlapping. Individuals initially belonging to the same species may begin to differentiate from each other when they start eating different foods or living in different habitats. If the slight genetic differences that may exist between such individuals are reinforced by assortive mating1, 2 populations may emerge and begin to diverge genetically and phenotypically to eventually become separate species. New species may originate even when there is some gene flow between the 2 populations. An intermediate mechanism is parapatric speciation, which takes place in contiguous, but otherwise geographically isolated (allopatric) populations. G.G. Simpson. 1983. Fossils and the History of Life. Scientific American Books. The late Ernst Mayr was a strong proponent of allopatric speciation and for most of his long career, he discounted sympatric speciation as a viable mechanism. However, an increasing number of studies have been demonstrating that sympatric speciation is possible and may have taken place more often than traditionally believed. A well-written short essay by Chris D. Jiggins2 in the 9 May issue of Current Biology reviews some recent studies and presents a good argument in favor of sympatric speciation, while pointing out that the usual division of speciation events along a strict line as either sympatric or allopatric creates an artificial dichotomy. In line with Mayrs opinion about the necessity to explain biological processes by more than one theory, Jiggins suggests that in most cases of speciation, sympatric and allopatric processes may both have been reponsible. allopatric and sympatric speciation lie at the opposite ends of a continuum, which runs from zero to maximal gene flow between diverging populations. These new studies provide good evidence that fully sympatric speciation can occur, but most examples probably lie somewhere in between these two extremes. As is usually the case with any genuine scientific controversy, this one will continue to inspire further research and lead to better understandings of the many-faceted speciation == Gavin de Beer and mosaic evolution In a broad sense, all organisms can be said to be mosaics, with some characteristics so ancient in origin that they have changed little and some so recent, geologically speaking, that they have changed more than a little. It rarely occurs to most of us that we share ancestral characters with such different organisms as, for example, a flowering shrub. On this date in 1972 the English evolutionary biologist Sir Gavin R. de Beer died (born 1899). One lasting contribution of de Beer to evolutionary theory was the concept of mosaic evolution that he developed in a 1954 paper1. Although a mosaic-like pattern of evolution is becoming more and more apparent in many major evolutionary transitions, including the evolution of humans from ape-like ancestors, I have not been able to find a recent general review of what mosaic evolution is all about. Stebbins published a review in 1983, but he seems to have confused mosaic evolution with adaptive radiation2. Recently, Mayr3 and earlier, Simpson4 gave brief explanations of the concept with both authors properly distinguishing mosaic evolution from adaptive radiation. Curiously, Ridleys textbook on evolution5 doesnt mention mosaic evolution at all. To my great satisfaction, however, I have found in de Beers succinctly written original paper a full explanation of his idea. As the title of his paper implies, de Beer derived the concept of mosaic evolution from his study of the fossil Archaeopteryx and by comparing it with the bones of reptiles and birds. He found that Archaeopteryx had both reptilian and avian features: All these are characters which would not be in the least out of place if found in any reptile. On the other hand, there are a number of features in Archaeopteryx which are absolutely characteristic of birds This comparison led him to conclude that it is clear that Archaeopteryx provides a magnificent example of an animal intermediate between two classes, the reptiles and the birds, with each of which it shares a number of well-marked characters. And this led to the formulation of mosaic evolution (content in brackets mine): the statement that an animal was intermediate might mean that it was a mixture and that the transition affected some parts of the animal and not others, with the result that some parts were similar to those of one type [ancestor], other parts similar to the other type [descendant], and few or no parts intermediate in structure. In such a case the animal might be regarded as a mosaic in which the pieces could be replaced independently one by one, so that the transitional stages were a jumble of characters some of them similar to those of the class from which the animal evolved, others similar to those of the class into which the animal was evolving. He then applied these ideas to the fossils exemplifying the transitions from fish to amphibian and from amphibian to reptile and finally, from reptile to mammal. In each case, his observations derived from specific examples can be turned into general statements of mosaic evolution. But the fact that an animal can be at one and the same time show so many features which would make it an ideal transitional form, and also spoil this picture by possessing one or two characters which rule it out as a direct ancestor, is itself an argument in support of the principle of mosaic evolution, with the different pieces evolving separately, and some of them too fast. This phenomenon is found again and again in the study of transitions from one type of animal to another, and appears to be of general applicability. It would be more difficult to understand if the transitions took place by a gradual and simultaneous conversion of all the parts of the animal. This was followed by the notion of the evolution of different organs at different rates: Just as in some casesan animal may show characters which have evolved too fast relatively to the other characters, in other cases certain characters may have been left in a profoundly archaic condition. De Beer even dealt preemptively with potential objections to his idea: Organisms are delicately balanced and adjusted mechanisms, and on the average, changes are more likely to upset than to strengthen them. Selection may therefore be expected to have acted with greater rigour against organisms vaying in more than one direction at a time, unless the directions were correlated All of this terminated in a final conclusion: A necessary consequence of mosaic evolution and of the independence of characters evolving at different rates is the production of animals showing mixtures of primitive and specialised characters. A technical paper discussing de Beers significant accomplishments in embryology. Some recent technical papers on mosaic evolution: Andrew N. Iwaniuk, Karen M. Dean, John E. Nelson. 2004. A mosaic pattern characterizes the evolution of the avian brain. Proceedings: Biological Sciences 271, S148151. Robert A. Barton and Paul H. Harvey. 2000. Mosaic evolution of brain structure in mammals. Nature 405, 1055-1058. Todd C. Rae. 1999. Mosaic Evolution in the Origin of the Hominoidea. Folia Primatol 70:125135 1. De Beer, G.R. 1954. Archaeopteryx and evolution. Advancement of Science 11:160-170. 2. Stebbins, G.L. 1983. Mosaic evolution: an integrating principle for the modern synthesis. Experientia 39:823-834. 3. Mayr, E. 2001. What evolution is. Basic Books. 4. Simpson, G.G. 1983. Fossils and the history of life. Scientific American Books. 5. Ridley, M. 1996. Evolution. 2nd ed. Blackwell. == Chimpanzees 'hunt using spears' Chimpanzees in Senegal have been observed making and using wooden spears to hunt other primates, according to a study in the journal Current Biology. Researchers documented 22 cases of chimps fashioning tools to jab at smaller primates sheltering in cavities of hollow branches or tree trunks. The report's authors, Jill Pruetz and Paco Bertolani, said the finding could have implications for human evolution. Chimps had not been previously observed hunting other animals with tools. Pruetz and Bertolani made the discovery at their research site in Fongoli, Senegal, between March 2005 and July 2006. "There were hints that this behavior might occur, but it was one time at a different site," said Jill Pruetz, assistant professor of anthropology at Iowa State University, US. "While in Senegal for the spring semester, I saw about 13 different hunting bouts. So it really is habitual." Chimpanzees were observed jabbing the spears into hollow trunks or branches, over and over again. After the chimp removed the tool, it would frequently smell or lick it. In the vast majority of cases, the chimps used the tools in the manner of a spear, not as probes. The researchers say they were using enough force to injure an animal that may have been hiding inside. However, they did not photograph the behaviour, or capture it on film. Adolescent females exhibited the behaviour most frequently (Image: M Gaspersic) In one case, Pruetz and Bertolani, , from the Leverhulme Centre for Human Evolutionary Studies in Cambridge, UK, witnessed a chimpanzee extract a bushbaby with a spear. In most cases, the Fongoli chimpanzees carried out four or more steps to manufacture spears for hunting. In all but one of the cases, chimps broke off a living branch to make their tool. They would then trim the side branches and leaves. In a number of cases, chimps also trimmed the ends of the branch and stripped it of bark. Some chimps also sharpened the tip of the tool with their teeth. Adult males have long been regarded as the hunters in chimp groups. But the authors of the paper in Current Biology said females, particularly adolescent females, and young chimps in general were seen exhibiting this behaviour more frequently than adult males. "It's classic in primates that when there is a new innovation, particularly in terms of tool use, the younger generations pick it up very quickly. The last ones to pick up are adults, mainly the males", said Dr Pruetz, who led the National Geographic-funded project. This is because young chimps pick the skill up from their mothers, with whom they spend a lot of their time. "It's a niche that males seem to ignore," Dr Pruetz told BBC News. Many areas where chimpanzees live are also home to red colobus monkey, which the chimps hunt. However, the Senegal site is lacking in this species, so chimps may have needed to adopt a new hunting strategy to catch a different prey - bushbaby. The authors conclude that their findings support a theory that females may have played a similarly important role in the evolution of tool technology among early humans. == http://en.wikipedia .org/wiki/ Micelle Micelles are phospholipid layers that form spontaneously in polar liquids such as water. If this sounds familiar, it is because plasma membranes of cells consist of phospholipid bilayers. The probability of phospholipid bilayers forming in water is 1. It happens every time. Pretty easy math. === Lactose Tolerance in East Africa Points to Recent Evolution A surprisingly recent instance of human evolution has been detected among the peoples of East Africa. It is the ability to digest milk in adulthood, conferred by genetic changes that occurred as recently as 3,000 years ago, a team of geneticists has found. The finding is a striking example of a cultural practice the raising of dairy cattle feeding back into the human genome. It also seems to be one of the first instances of convergent human evolution to be documented at the genetic level. Convergent evolution refers to two or more populations acquiring the same trait independently. Throughout most of human history, the ability to digest lactose, the principal sugar of milk, has been switched off after weaning because the lactase enzyme that breaks the sugar apart is no longer needed. But when cattle were first domesticated 9,000 years ago and people later started to consume their milk as well as their meat, natural selection would have favored anyone with a mutation that kept the lactase gene switched on. Such a mutation is known to have arisen among an early cattle-raising people, the Funnel Beaker culture, which flourished 5,000 to 6,000 years ago in north-central Europe. People with a persistently active lactase gene have no problem digesting milk and are said to be lactose tolerant. Almost all Dutch people and 99 percent of Swedes are lactose tolerant, but the mutation becomes progressively less common in Europeans who live at increasing distances from the ancient Funnel Beaker region. Geneticists wondered if the lactose tolerance mutation in Europeans, identified in 2002, had arisen among pastoral peoples elsewhere. But it seemed to be largely absent from Africa, even though pastoral peoples there generally have some degree of tolerance. A research team led by Dr. Sarah Tishkoff of the University of Maryland has now solved much of the puzzle. After testing for lactose tolerance and genetic makeup among 43 ethnic groups in East Africa, she and her colleagues have found three new mutations, all independent of one another and of the European mutation, that keep the lactase gene permanently switched on. The principal mutation, found among Nilo-Saharan-speaking ethnic groups of Kenya and Tanzania, arose 2,700 to 6,800 years ago, according to genetic estimates, Dr. Tishkoffs group reports today in the journal Nature Genetics. This fits well with archaeological evidence suggesting that pastoral peoples from the north reached northern Kenya about 4,500 years ago and southern Kenya and Tanzania 3,300 years ago. Two other mutations were found, among the Beja people of northeastern Sudan and tribes of the same language family, Afro-Asiatic, in northern Kenya. Genetic evidence shows that the mutations conferred an enormous selective advantage on their owners, enabling them to leave almost 10 times as many descendants as people without such mutations. The mutations have created one of the strongest genetic signatures of natural selection yet reported in humans, the researchers write. The survival advantage was so powerful perhaps because those with the mutations not only gained extra energy from lactose but also, in drought conditions, would have benefited from the water in milk. People who were lactose intolerant could have risked losing water from diarrhea, Dr. Tishkoff said. Diane Gifford-Gonzalez, an archaeologist at the University of California, Santa Cruz, said the new findings were very exciting because they showed the speed with which a genetic mutation can be favored under conditions of strong natural selection, demonstrating the possible rate of evolutionary change in humans. The genetic data fitted in well, she said, with archaeological and linguistic evidence about the spread of pastoralism in Africa. The first clear evidence of cattle in Africa is from a site 8,000 years old in northwestern Sudan. Cattle there were domesticated independently from two other domestications, in the Near East and the Indus Valley of India. Nilo-Saharan speakers in Sudan and their Cushitic-speaking neighbors in the Red Sea hills probably domesticated cattle at the same time, because each has an independent vocabulary for cattle items, said Dr. Christopher Ehret, an expert on African languages and history at the University of California, Los Angeles. Descendants of each group moved south and would have met again in Kenya, Dr. Ehret said. Dr. Tishkoff detected lactose tolerance among Cushitic speakers and Nilo-Saharan groups in Kenya. Cushitic is a branch of Afro-Asiatic, the language family that includes Arabic, Hebrew and ancient Egyptian. Dr. Jonathan Pritchard, a statistical geneticist at the University of Chicago and a co-author of the new article, said there were many signals of natural selection in the human genome but it was usually hard to know what was being selected for. In this case Dr. Tishkoff clearly defined the driving force, he said. The mutations Dr. Tishkoff detected are not in the lactase gene itself but a nearby region of the DNA that controls the activation of the gene. The finding that different ethnic groups in East Africa have different mutations is one instance of their varied evolutionary history and their exposure to many different selective pressures, Dr. Tishkoff said. There is a lot of genetic variation between groups in Africa, reflecting the different environments in which they live, from deserts to tropics, and their exposure to very different selective forces, she said. People in different regions of the world have evolved independently since dispersing from the ancestral human population in northeast Africa 50,000 years ago, a process that has led to the emergence of different races. But much of this differentiation at the level of DNA may have led to the same physical result. As Dr. Tishkoff has found in the case of lactose tolerance, evolution may use the different mutations available to it in each population to reach the same goal when each is subjected to the same selective pressure. I think its reasonable to assume this will be a more general paradigm, Dr. Pritchard said. == There are hundreds of scientific research articles about evolution published each and every year. Here's a selection of professional science journals (in the U.S. and the U.K.) that routinely or exclusively publish professional scientific research concerning evolution: PLoS Biology (published by the Public Library of Science) http://biology. plosjournals. org/ PLoS Genetics (published by the Public Library of Science) http://genetics. plosjournals. org/ Science (published by the American Association for the Advancement of Science) http://www.sciencem ag.org/ Nature http://www.nature. com/ Journal of Biology (published by BioMed Central) http://jbiol. com/ Journal of Evolutionary Biology http://www.blackwel lpublishing. com/journal. asp?ref=1010- 061X view online content: http://www.blackwel l-synergy. com/rd.asp? code=JEB& goto=journal International Journal of Organic Evolution http://evol. allenpress. com/evolonline/ ?request= index-html# Evolution_ Journal [link may be line-wrapped] Molecular Biology and Evolution (published by the Society for Molecular Biology and Evolution) http://www.mbe. oupjournals. org Evolution & Development http://www.blackwel lpublishing. com/journal. asp?ref=1520- 541X Trends in Ecology & Evolution http://www.elsevier .com/wps/ find/journaldesc ription.cws_ home/30339/ description [link may be line-wrapped] Trends in Genetics http://www.elsevier .com/wps/ find/journaldesc ription.cws_ home/405918/ description [link may be line-wrapped] Integrative and Comparative Biology (Journal of the Society for Integrative and Comparative Biology; published as the American Zoologist from 1961 to 2001) http://www.sicb. org/az/ Invertebrate Biology (Journal of the American Microscopical Society) http://www.inverteb ratebiology. org/ Proceedings of the National Academy of Sciences (PNAS) Biological Sciences http://www.pnas. org/current. shtml#BIOLOGICAL _SCIENCES Palobiology Journal of Paleontology (both published by The Paleontological Society) http://www.psjourna ls.org/paleoonli ne/?request= get-archive The Journal of Vertebrate Paleontology (published by the Society of Vertebrate Paleontology) http://www.vertpale o.org/jvp/ Paleontologia Electronica http://palaeo- electronica. org/ Cladistics The International Journal of the Willi Hennig Society http://www.blackwel lpublishing. com/journal. asp?ref=0748- 3007 Evolution International Journal of Organic Evolution http://evol. allenpress. com/evolonline/ ?request= get-archive Biological Journal of the Linnean Society http://www.blackwel lpublishing. com/journal. asp?ref=0024- 4066 Zoological Journal of the Linnean Society http://www.blackwel lpublishing. com/journal. asp?ref=0024- 4082 Botanical Journal of the Linnean Society http://www.blackwel lpublishing. com/journal. asp?ref=0024- 4074 Evolutionary Ecology (published in the Netherlands) http://www.springer .com/west/ home/life+ sci?SGWID= 4-10027-70- 35681186- 0 [link may be line-wrapped] Genetics http://www.genetics .org/ Molecular Phylogenetics and Evolution http://www.elsevier .com/wps/ find/journaldesc ription.cws_ home/622921/ description [link may be line-wrapped] Proceedings of the Royal Society: Biological Sciences http://www.pubs. royalsoc. ac.uk/index. cfm?page= 1087 Journal of Zoological Systematics and Evolutionary Research http://www.blackwel lpublishing. com/journal. asp?ref=0947- 5745 Evolutionary Bioinformatics Online http://www.la- press.com/ evolbio.htm === Public acceptance of evolution Human beings, as we know them, developed from earlier species of animals: true or false? This simple question is splitting America apart, with a growing proportion thinking that we did not descend from an ancestral ape. A survey of 32 European countries, the US and Japan has revealed that only Turkey is less willing than the US to accept evolution as fact. Religious fundamentalism, bitter partisan politics and poor science education have all contributed to this denial of evolution in the US, says Jon Miller of Michigan State University in East Lansing, who conducted the survey with his colleagues. "The US is the only country in which [the teaching of evolution] has been politicised," he says. "Republicans have clearly adopted this as one of their wedge issues. In most of the world, this is a non-issue." Miller's report makes for grim reading for adherents of evolutionary theory. Even though the average American has more years of education than when Miller began his surveys 20 years ago, the percentage of people in the country who accept the idea of evolution has declined from 45 in 1985 to 40 in 2005 (Science, vol 313, p 765). That's despite a series of widely publicised advances in genetics, including genetic sequencing, which shows strong overlap of the human genome with those of chimpanzees and mice. "We don't seem to be going in the right direction," Miller says. There is some cause for hope. Team member Eugenie Scott of the National Center for Science Education in Oakland, California, finds solace in the finding that the percentage of adults overtly rejecting evolution has dropped from 48 to 39 in the same time. Meanwhile the fraction of Americans unsure about evolution has soared, from 7 per cent in 1985 to 21 per cent last year. "That is a group of people that can be reached," says Scott. The main opposition to evolution comes from fundamentalist Christians, who are much more abundant in the US than in Europe. While Catholics, European Protestants and so-called mainstream US Protestants consider the biblical account of creation as a metaphor, fundamentalists take the Bible literally, leading them to believe that the Earth and humans were created only 6000 years ago. Ironically, the separation of church and state laid down in the US constitution contributes to the tension. In Catholic schools, both evolution and the strict biblical version of human beginnings can be taught. A court ban on teaching creationism in public schools, however, means pupils can only be taught evolution, which angers fundamentalists, and triggers local battles over evolution. These battles can take place because the US lacks a national curriculum of the sort common in European countries. However, the Bush administration's No Child Left Behind act is instituting standards for science teaching, and the battles of what they should be has now spread to the state level. Miller thinks more genetics should be on the syllabus to reinforce the idea of evolution. American adults may be harder to reach: nearly two-thirds don't agree that more than half of human genes are common to chimpanzees. How would these people respond when told that humans and chimps share 99 per cent of their genes? == Paleontologists Find Species With Links to 'Lucy Skeleton' In following the fossil tracks of human evolution, scientists have for years searched for links between Australopithecus, the kin of the famous "Lucy" skeleton, and even earlier possible ancestors. Now, they think they have found some connections in Ethiopia. An international team of paleontologists is reporting the discovery of transitional species superimposed in sediments in the neighborhood of a single site. Tim D. White, a paleontologist at the University of California, Berkeley, who was a leader of the team, and his colleagues said the 4.1-million-year-old fossils were anatomically intermediate between the earlier species Ardipithecus ramidus and the later species Australopithecus afarensis, the Lucy family. The newfound bones and teeth are the earliest remains of the most primitive Australopithecus, known as anamensis. "This new discovery closes the gap between the fully blown australopithecines and earlier forms we call Ardipithecus," Dr. White said in a statement. "We now know where Australopithecus came from before four million years ago." The scientists said the fossils supported the hypothesis that Australopithecus anamensis was a direct ancestor of afarensis, which lived between 3.6 million and 3 million years ago. The Australopithecus genus resembling apes in stature and small brain but unlike the great apes in that it walked on two legs is thought to have given rise to our own genus, Homo. Some later australopithecines survived until about 1.2 million years ago, existing in Africa as contemporaries with Homo erectus, a predecessor of modern humans. The genus Ardipithecus, discovered by Dr. White in 1992, appears to have lived between 5.7 million and 4.4 million years ago. It was even more apelike, but also walked on two legs. The relationship between Ardipithecus and Australopithecus, scientists said, remains unclear because of the wide gap in their chronology. Still, they suggested that one probably led to another. Dr. White said in a telephone interview that a key to interpreting the new anamensis was where it was discovered, in the Middle Awash valley of the Afar Region of Ethiopia. The area, about 140 miles northeast of Addis Ababa, Ethiopia's capital, has also yielded critical evidence of afarensis and the ramidus species of Ardipithecus. "Finding these three things in time sequence in a single place, that's never happened before," Dr. White said. In the journal report, the scientists said the evidence suggested "a relatively rapid shift from Ardipithecus to Australopithecus in this region of Africa." The new anamensis fossils were uncovered first at Aramis and then at a place called Asa Issie. The teeth and jawbones of eight individuals were found at Asa Issie, the most recent of the discoveries coming last December. The fieldwork and analysis was conducted by scientists from Ethiopia, Japan, France and the United States, with support from the National Science Foundation. Giday WoldeGabriel, a geologist at the Los Alamos National Laboratory and another leader of the team, said the abundance of monkey and other mammal bones and petrified wood found at the sites showed that this was a woodland ecology between four million and six million years ago. == Early Land Animals Could Walk And Run Like Mammals, New Study Finds Salamanders and the tuatara, a lizard-like animal that has lived on Earth for 225 million years, were the first vertebrates to walk and run on land, according to a recent study by Ohio University researchers. The tuatara, a lizard-like animal that has lived on Earth for 225 million years, was one of the first vertebrates to run and walk, scientists found. (Courtesy of Steve Reilly, Ohio University) After studying the creatures at the Toledo Zoo, Stephen Reilly, associate professor of biological sciences, and doctoral student Eric McElroy determined that they use both forms of locomotion, which are energy-saving mechanisms generally believed to be important only in fast-running animals such as mammals and birds. The research was published in the March 8 issue of the journal Proceedings of the Royal Society B: Biological Sciences. Andrew Odum, curator of herpetology at the Toledo Zoo, and Valerie Hornyak, head herpetology keeper, were co-authors of the study. Tuataras, which are usually about 1 to 2 feet long, look like large lizards with green or brown scales and short spikes on their backs. They have unique anatomical features that are somewhere between those of lizards and birds. The critters are found only in New Zealand, where the cool climate is ideal for these animals that cant survive in temperatures above 25 degrees Celsius (77 degrees Fahrenheit). The animals can grow as old as 100 years, and live mostly off of insects, eggs and small birds. Fossil records show that the tuatara lived on Earth as early as 225 million years ago and hasnt changed significantly over time. Tuataras are the oldest living models of early tetrapods (four-legged animals) still alive today; thats what makes them so interesting, Reilly said. In the recent study, the tuataras and salamanders walked and ran on a trackway with an integrated plate that measured the force with which the animals hit the ground with each step. From videotapes and the force measurements, the researchers could tell when the animals were walking or running. The difference is not obvious in these critters, which tend to move with a slow, lumbering gait. Thats led scientists to believe that the primitive animals could only walk. But force data used to study the movement of these creatures center of mass showed otherwise. In walking, the center of mass vaults up and over the limbs with each step. In running, the center of mass dips with each step, and tendons and joints in the legs act as biological springs. Mammals such as humans, dogs and horses can use both mechanisms to conserve up to 50 percent of their energy needed to walk and run. When studying salamanders and tuataras, the researchers spotted the telltale vault and dip of center of mass movements in different strides confirmation that the creatures mechanically walk and run. Because they are the oldest living examples of four-legged animals, the new findings suggest that both energy saving mechanisms appeared when the first vertebrates moved onto land, Reilly explained. In comparison to previous research on other vertebrates, this also suggests that all terrestrial vertebrates except for turtles, which are limited by their shell can walk and run. The researchers also showed, however, that walking and running in tuataras occur at the same speed and use about the same amounts of energy. Reilly believes that this could be a pre-adaptation in these primitive animals that have not evolved the need for speed, unlike other animals. The research, which was funded by the National Science Foundation and the Research Challenge Program at Ohio University, also shows for the first time a clear difference in locomotor mechanics between lumbering animals with clumsy, ungraceful gaits and cursorial animals that move fast and smoothly. In lumbering animals, up and down movements dominate the mechanical energy of locomotion. These movements are smoothed out in cursorial animals such as in dogs and horses, where more energy is shifted to forward movement, and the center of mass oscillates relatively less with each step. Reilly and McElroy were interested in tuataras not only because they are a living fossil, but also because tuataras are a threatened species, according to the World Conservation Union. Tuataras only survive on a few small islands off New Zealand, and I would really like to study their locomotor behavior in the wild, Reilly said. Given their status as the worlds oldest known living tetrapod, knowing more about how these animals move in nature is critical to our understanding of vertebrate evolution. == Is water the answer to natures handedness? January 2006 Water molecules cause biological systems to prefer left-handed chiral centres, say scientists from Israel and the US. All amino acids found in living organisms have left-handed chirality, even though left- and right-handed amino acids should chemically be the same. Meir Shinitzky and colleagues at the Weizmann Institute of Science believe the humble water molecule to be responsible. Shinitzky dissolved polymers of left- and right-handed amino acids in water, and measured the pH at which they denatured from helices to random coils. This was 0.2 to 0.3 units higher for the right-handed molecules, which implied they were less stable. The effect disappeared when heavy water (D2O) was used. The group discounted undetectable impurities in the water as the cause. In most of our experiments with heavy water, where the differences are virtually eliminated, 20 per cent light water was still present, said Shinitzky. "The ultimate challenge is the possibility that the function of a mirror-image biological system would be inferior to its natural counterpart" - Meir Shinitzky Water molecules exist in two forms,ortho-H2O andpara-H2O. The interchange between these forms in liquid water is very slow, taking minutes, so an average form is not established. There is also a tiny difference in the magnetic fields of left-handed and right-handed chiral centres. Shinitzkys group suggests that the different interactions between the weak magnetic field ofortho-H2O and the magnetic fields of left- and right-handed amino acids is sufficient to account for the pH measurements. This is a controversial explanation, because the energy difference between molecule types is tiny yet the effect on denaturing is huge according to Jeanne Crassous at the University of Rennes, France. Crassous said she would like to see the results and the role of water impurities corroborated by another research group. Shinitzkys next step is to compare the structures and catalytic activities of left- and right-handed biological molecules. The ultimate challenge is the possibility that the function of a mirror-image biological system would be inferior to its natural counterpart, he said. References Y Scolnik, I Portnaya, U Cogan, S Tal, R Haimovitz, M Fridkin, A C Elitzur, D W Deamer and M Shinitzky,Phys. Chem. Chem. Phys., 2006,8, 333 (DOI : 10.1039/b513974k) == Most human-chimp differences due to gene regulation not genes http://tinyurl.com/s3lh3 http://www.eurekalert.org/pub_releases/2006-03/uocm-mhd030606.php Although their genes are virtually identical, humans and chimpanzees differ substantially. This study provides powerful new evidence for a 30-year-old theory, that the differences are due more to changes in gene regulation than differences in individual genes. Using novel technology, researchers show that genes for transcription factors, which influence the activity of many genetic targets, were four times as likely to have changed their own expression patterns as the genes they regulate. == Evolutionary paths to new therapeutic drugs, as well as a wide assortment of other enzyme products, have been created through, of all things, intelligent design. A team of researchers with the Lawrence Berkeley National Laboratory (Berkeley Lab) and the University of California at Berkeley have developed a technique in which the evolution of an important class of proteins is steered towards a desired outcome. "We've taken enzymes that are promiscuous, meaning they have the capacity to evolve along many different functional lines, and trained them to become specialists," said chemical engineer Jay Keasling, who led this stud The results of this study were reported in the February 22, 2006, on- line edition of the journal Nature. According to the theory of divergent molecular evolution, primordial enzymes and other proteins started out as "promiscuous" so that primitive organisms would be better able to adapt to their environment. Driven by selective pressures, these promiscuous enzymes and other proteins evolved along divergent lines to acquire the specialized functions needed by a host organism to survive. "This process is highly dependent on the fact that the functions of promiscuous proteins can be altered with just a small number of amino acid substitutions, a property known as plasticity," said Keasling. "It was our contention that the application of the theory of divergent molecular evolution to promiscuous enzymes would enable us to design enzymes with greater specificity and higher activity." To test this idea, Keasling and his students worked with a type of naturally occurring hydrocarbon compounds, called sesquiterpenes, that is widely used in a variety of products. For their model enzyme, they selected a sesquiterpene synthase produced by the Grand fir tree, which has the capacity to develop into any of 52 different sesquiterpenes from a sole substrate. "This Grand fir sesquiterpene synthase represents the ultimate in promiscuous enzymes," said Yoshikuni. "We were able to take it and construct seven specific and active enzymes synthases. These seven enzymes use different reaction pathways to produce specific products that are as diverse as they can be from one another." In nature, the divergent evolution of promiscuous enzymes is achieved through trial and error, similar to the way in which the human immune system works. Multiple combinations of many different amino acid substitutions are tested in promiscuous enzymes until an evolutionary path that achieves a desired result is found. The amino acid substitutions that significantly drive molecular evolution are called "plasticity residues." The Berkeley researchers identified the plasticity residues for the Grand fir sesquiterpene synthase, then systematically recombined mutations of these residues through site-directed mutagenesis, based on a mathematical model developed by Yoshikuni. Construction of the seven sesquiterpene synthases was accomplished with the screening of fewer than 2,500 mutants. An alterative approach, called directed evolution or molecular breeding, that is currently being tested at other laboratories, requires the screening of tens of thousands to a million or more mutants. "The enzyme synthase was there ready to be evolved, and with our methodology, we were able to rapidly and efficiently evolve it down a pathway of our choice," Keasling said. "We are recapitulating evolution into intelligent design. In the case of this particular Grand fir enzyme synthase, it naturally makes a soup of small amounts of 52 different products. We were able to focus it instead on making large amounts of one of seven of those products." While the researchers have not yet reached the point where they can design a promiscuous enzyme to make any kind of product they want, even one that does not occur in nature, this demonstration represents a significant step in that direction. The idea would be to one day be able to design an enzyme synthase that would evolve along a specific functional pathway to yield a desired molecular product, then introduce it into microbes for mass production. In addition to synthesizing therapeutic drugs, other possible applications would include flavors, fragrances and nutraceuticals. == New Evidence That Natural Selection Is A General Driving Force Behind The Origin Of Species Charles Darwin would undoubtedly be both pleased and chagrined: The famous scientist would be pleased because a study published this week finally provides the first clear evidence that natural selection, his favored mechanism of evolution, drives the process of species formation in a wide variety of plants and animals. But he would be chagrined because it has taken nearly 150 years to do so. What Darwin did in his revolutionary treatise "On the Origin of Species" was to explain how many of the extraordinary biological traits possessed by plants and animals arise from a single process, natural selection. Since then a large number of studies and observations have supported and extended his original work. However, linking natural selection to the origin of the 30 to 100 million different species estimated to inhabit the earth, has proven considerably more elusive. In the last 20 years, studies of a number of specific species have demonstrated that natural selection can cause sub-populations to adapt to new environments in ways that reduce their ability to interbreed, an essential first step in the formation of a new species. However, biologists have not known whether these cases represent special exceptions or illustrate a general rule. The new study, published online in the Proceedings of the National Academy of Sciences, provides empirical support for the proposition that natural selection is a general force behind the formation of new species by analyzing the relationship between natural selection and the ability to interbreed in hundreds of different organisms a" ranging from plants through insects, fish, frogs and birds a" and finding that the overall link between them is positive. Filling a gap in evolutionary studies "This helps fill a big gap that has existed in evolutionary studies," says Daniel Funk, assistant professor of biological sciences at Vanderbilt University. He authored the study with Patrik Nosil from Simon Fraser University in British Columbia and William J. Etges from the University of Arkansas. "We have known for some time that when species invade a new environment or ecological niche, a common result is the formation of a great diversity of new species. However, we haven't really understood how or whether the process of adaptation generally drives this pattern of species diversification." The specific question that Funk and his colleagues set out to answer is whether there is a positive link between the degree of adaptation to different environments by closely related groups (termed ecological divergence) and the extent to which they can interbreed (termed reproductive isolation.) Funk and his colleagues saw a way to address this question by extending a method pioneered by Jerry A. Coyne, University of Chicago, and H. Allen Orr, University of Rochester in a now classic study of speciation in fruit flies published in 1989. Coyne and Orr were interested in exploring how the process of species formation develops over time. To measure this process, known as speciation, they developed an index of reproductive isolation. For a measure of time, they used the fact that genetic mutations accumulate over time. So if the percent difference in the genomes of species A and B differs by five percent while the difference between A and C differs by 10 percent, then the time since A and C diverged is about twice that since A and B split apart. Extending the methodology of a classic, 1989 study Coyne and Orr's approach provided a number of valuable insights into the speciation process, such as showing that a certain amount of time must pass before reproductive isolation evolves and that it isn't a sudden but a gradual process. Other researchers were impressed with the power of their method and applied it to a number of other groups of creatures. In Coyne and Orr's book, Speciation, published in 2004, the scientists listed eight different studies that applied their approach to flowering plants, birds in general, doves in particular, fruit flies, butterflies, frogs, fish in general, and a specific type of fish called darters. Together, the studies evaluated many hundreds of species. "I got the idea that we could extend the analysis into a third dimension, ecological divergence," says Funk. He realized that applying this new approach to data from each of the eight studies would have two major advantages: Freedom from bias. The studies that had been previously subjected to the Coyne and Orr analysis provided the researchers with an unbiased sample. Many of the individual case studies that have found a role for natural selection were picked for study because the investigators detected indications that this was the case and so, as a group, the cases suffer from a pro-natural-selection bias. Eliminating the time factor. The results of previous speciation studies have been clouded by the effects of time. Regardless of the role that natural selection plays, random mutations are bound to increase the reproductive isolation between two groups over time. In earlier studies, it has been difficult a" if not impossible a" to disentangle the two effects. With the proposed approach, however, the authors could apply a widely used mathematical procedure, called regression analysis, to factor out time's effects and isolate the impact of natural selection. "We thought that the idea itself was important, that this is a really powerful approach to a very major question," says Funk, "but we thought that there was no way in the world that we were actually going to get statistically significant results." Problem posed by lack of uniformity of ecological data The reason for his doubt was the incompleteness and lack of uniformity of ecological data. "There are all these species out there and so few of them are known in intimate detail, so any kind of ecological characterization, through no fault of ecologists, will be limited in accuracy and precision," Funk says. Nevertheless, the researchers decided to do the best they could with the information available. Specifically, they collected information from the published literature on three basic ecological variables: habitat, diet and size. They reasoned that evaluating the degree to which a pair of species differed from each other in these variables would provide an idea of to what degree natural selection had caused them to diverge evolutionarily. Next they used this information to calculate estimates of ecological divergence for each pair of species from each of the eight original studies. For example, if one species of bird eats fruit, insects and nuts and the second species eats fruit, insects and meat, then their estimate of ecological divergence in diet is one third. Similarly, if the average weight of one species of bird is 4 ounces and that of the other is 5 ounces, then the estimate of ecological divergence in size is 25 percent. When they compared the ecological divergence estimates with the degree of reproductive isolation for each of hundreds of pairs of species from the original studies, they found that the overall association was positive with a surprisingly high level of confidence: The odds that these findings are simply due to chance are only one in 250, substantially higher than the standard confidence level of one chance in 20 that scientists demand. "The fact that the association is statistically significant despite the crudeness of our estimates suggests that the true biological association is very strong," Funk says. "Darwin's famous book was called 'On the Origin of Species,' but it was really about natural selection on traits rather than speciation. Since our study suggests that natural selection is a general cause of speciation, it seems that Darwin chose an appropriate title after all." == He's fat, ugly and poisonous -- and he's mutating. He's the cane toad (Bufo marinus), a species which was introduced into the Australian state of Queensland 70 years ago to tackle insect pests in canefields and has since become an ecological catastrophe. Weighing in at to up two kilos (4.4 pounds), the unwanted anuran has extended its range to more than a million square kilometers (386,000 square miles) in tropical and sub-tropical Australia, crushing native species in its relentless advance. A team of University of Sydney toad watchers positioned themselves on the front line of the invasion, 60 kilometers (35 miles) east of the city of Darwin, and for 10 months caught toads, some of which they radiotagged and let loose again. They were astonished to find that the creatures can hop up to 1.8 kms (1.1 miles) a night during wet weather, a record for any frog or toad. But even more remarkable was the discovery that the first toads to arrive at the front invariably had longer hind legs than those which arrived later. By comparison, the toads which are living in the long-established Queensland colonies have much shorter legs. The case is being seen as a classic example of Darwinian evolution -- animals that are stronger, faster or smarter are able to stake out new territory and defend it against those that are weaker, slower or less astute. The findings also neatly explain a puzzle surrounding the cane toad. From the 1940s to 1960s, the critter expanded its range by only 10 kms (six miles) a year. Today, though, it is advancing at the rate of more than 50 kms (30 miles) annually. The reason: with longer legs, the mutating species is able to travel further, faster. == From So Simple a Beginning: The Four Great Books of Charles Darwin Edited by Edward O. Wilson (W. W. Norton, 1,706 pp., $39.95) Darwin: The Indelible Stamp: The Evolution of an Idea Edited by James D. Watson (Running Press, 1,260 pp., == One of the important biological differences is between prokaryotic and eukaryotic cells. I have not read any ID discussions of this difference. I suspect that the only possible scientific question generated by ID is 'when were these two types of cells created'. Can anyone know of any other question raised by the ID proponents about this difference? For evolutionists, eukaryotic cells have been a puzzle. Because they are more complex than prokaryotes, it was reasonable that they would appear in the fossil record later than the simpler cells. However, to have evolved successfully, the first eukaryotic organism would have had to out-compete prokaryotes. This puts a serious constraint on the evolutionary process. At the same time, there seemed to be no reason why evolution would have given mitochondria and chloroplasts their own DNA. I think a simple, but effective, method of judging scientific theories is to consider whether later information tend to confirm the theory, or does it produce additional problems. For mitochondria and chloroplasts, there have been suggestions for at least 100 years that they originated as free-living prokaryotic cells. Lynn Margules became a strong advocate of this idea after it was found that mitochondria contained some DNA of their own. Since then, there have been a number of other findings. For instance, the DNA in mitochondria has been found to be more closely related to that of Rickettsia than to any eukaryotic nuclear DNA. Rickettsia bacteria are obligate intracellular pathogens, (causing typhus among other diseases) that are dependent on entry, growth, and replication within the cytoplasm of a eukaryotic host cell. The host cell then lysis and releases the rickettsial progeny to initiate a new infection cycle. Obviously an ancient single-celled organism infected with a pathogen like this, but which evaded cell breakdown would be a candidate for ancestor of all cells containing mitochondria. Also, some of the nuclear DNA in eukaryotes is also similar to than in Ricketsia. Studies have shown that some DNA in mitochondria can be released into the cell fluid and then incorporated into nuclear DNA. It was also found that mitochondria have their own ribosymes, coded by with part of the mitochondrian DNA, and in some organisms the mitochondrial genetic code is slightly different from the code used for translation of nuclear mRNA in the same organisms. www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=mcb.table.2307 All of these facts reinforce the endosymbiotic theory. In addition other organelles have been discovered. For example, hydrogenosomes are an anaerobic analogue of mitochondria which produce hydrogen and ATP in some anaerobic eukaryotic cells. In many cases hydrogenosomes contain no DNA, but some do contain a small amount. Another reasonable test is whether the same process (endosymbiosis in this case) is known to have occurred in other and situations which can be studied independently. Some information about endosymbiotic bacteria in three different species of aphid is at:- http://www.pnas.org/cgi/reprint/100/2/581 Symbiosis generally assumes mutual benefit. However, one partner may be more of a slave, exploited for the benefit of the host, or a parasite exploiting the host. This raises interesting questions as to how the partnership can be regulated. http://biology.plosjournals.org/perlserv/ Difficulties in regulation may have led to the extinction of many unsuccessful pairings. == Scorpion bigger than human described A geologist working in Scotland has uncovered footprints that he says come from The tracks were made about 330 million years ago by a six-legged creature called Hibbertopterus, according to Martin Whyte of the University of Sheffield, U.K. Hibbertopterus was some 1.6 metres (514 feet) long and a metre (314 feet) wide, he added. The tracks show that this now-extinct group of animals, previously thought to dwell in water only, could also survive on land, according to Whyte. At around the same time as the creature lived, scientists believe our own four-limbed ancestors were also making their first steps towards leaving the water and colonizing the land. The six-metre-long trackway reveals strides that were 27 cm (11 inches) long, and also features a central groove left by the creatures dragging tail, according to Whyte. This, he added, shows the creature was probably a very slow, lumbering beast when moving on land. == Stubby-Headed Crocodile Lurked in the Cretaceous Deep The oceans, coastlines and rivers of 135 million years ago crawled with crocodiles. Fossils of these beasts run the gamut from small to giant, but the ones known to science have all shared the long snout associated with modern crocs. Until now. Researchers say they have unearthed the remains of a large crocodile that looks very unlike its brethren in having a short, stubby snout. == If we could go back to about half of the earths history it is then that we'd find the earliest beginnings of life. The first half of earth's history began with a cooling period with the formation of continents called cratons. Cratons float and swirl on top of the earth's magma. Spain and Portugal are a micro continent all unto itself. It was once out in equatorial Atlantic and came to Europe traveling in a northeasterly direction. In recent geologic time it slammed into Europe, spinning in a counter clockwise direction, pushing up the Pyrenees Mountains and continues to do so. Italy once laid on its side against North Africa. That is, it boot shape laid in an east west direction. It split off from Africa spinning in a clockwise direction and sliding in a northerly direction. It slammed into Europe pushing up the great Swiss Alps. But before any of those events happened, Africa, Iran, the Middle East and India all laid much further south than Europe and Asia. This left a swath of water called the Great Tethys Seaway. The Black Sea, Caspian Sea and Mediterranean Sea are remnants of that seaway. The Black and Caspian have been pinched off from the advancing continents from the south. The Mediterranean Sea will soon be pinched closed as well. India is the fastest of all the continents and is moving in a northly direction. India is what's pushing up the Himalayas. And very near the top of Mount Everest are fossilize seashells giving testimony that there was indeed a Great Tethys Seaway. The fossils also humbles us to the core to understand that what was once at the bottom, is now on top. The human mind can barely comprehend the time it took to do that. == In the early Urey-Miller experiments, they were able to form 17 out of 20 amino acids involved in protein synthesis using just water (H2O), methane (CH4), ammonia (NH3) and hydrogen (H2). All the purines and pyrimidines involved synthesis of nucleic acid were formed. (The abiotic synthesis of ribose has proven to be more difficult -- but then again, we don't have an entire ocean with varying conditions and millions of years available in most lab experiments -- and you only need to create the spark of life once!) This experiment presupposed a reducing atmosphere (no oxygen). This assumption fell out of favor, throwing these experiments into question. For this reason, I had favored thermal vents in the oceans for a while. However, more recently, it appears that Urey and Miller had just about the right mix of atmosphere after all. == * Insight Into Eye Evolution Deals Blow To Intelligent Design 23 September 2005 How complex and physiologically remarkable structures such as the human eye could evolve has long been a question that has puzzled biologists. But in research reported this week in Current Biology, the evolutionary history of a critical eye protein has revealed a previously unrecognized link between certain components of sophisticated vertebrate eyes - like those found in humans - and those of the primitive light-sensing systems of invertebrates. The findings, from researchers at the University of Oxford, the University of London and Radboud University in The Netherlands, put in place a conceptual framework for understanding how the vertebrate eye, as we know it, has emerged over evolutionary time. Human sight relies on the ability of our eye to form a clear, focused image on the retina. Critical to this function is the eye lens and the physical properties that underlie the transparency of the lens. The eye's ability to precisely refract light is because of high concentrations of special proteins called crystallins found in lens cells. Vertebrates such as fish, frogs, birds, humans and other mammals all experience image- forming vision because our eyes express crystallins, which helps form the lens that is needed. But our invertebrate relatives, such as sea squirts, have only simple eyes that detect light but are incapable of forming an image. This lead to the view that the lens evolved within vertebrates early in vertebrate evolution, raising the question: How could a complex organ with such remarkable physical properties have evolved in the first place? Researcher Sebastian Shimeld from Oxford approached this question by examining the evolutionary origin of one crystallin protein family, known as the -crystallins. Focusing on sea squirts, the researchers found that these creatures possess a single crystallin gene, which is expressed in its primitive light-sensing system. The identification of this single crystallin gene strongly suggests that it is the gene from which the more complex vertebrate - crystallins evolved. Perhaps even more remarkable is the finding that _expression of the sea squirt crystallin gene is controlled by genetic elements that also respond to the factors that control lens development in vertebrates. This was demonstrated when regulatory regions of the sea squirt gene were transferred to frog embryos where they drove gene _expression in the tadpoles' own visual system, including the lens. The researchers say this suggests that prior to the evolution of the lens, there was a regulatory link between two tiers of genes, those that would later become responsible for controlling lens development, and those that would help give the lens its special physical properties. This combination of genes appears to have then been selected in an early vertebrate during the evolution of its visual system, giving rise to the lens. The new findings deal a serious blow to the Intelligent Design movement which has long contended that the lack of an apparent evolutionary pathway for complex eye development indicated the presence of a supreme designer. Ref: Current Biology, Vol. 15, pages 1684-1689, September 20, 2005. DOI 10.1016/j.cub.2005.08.046 === http://www.gcssepm.org/special/cuffey_05.htm mammal-like reptiles == How old is Lucy? The hominid-bearing sediments in the Hadar formation are divided into three members. Lucy was found in the highest of these -- the Kada Hadar, or KH -- member. While fossils cannot be dated directly, the deposits in which they are found sometimes contain volcanic flows and ashes, which can now be dated with the 40Ar/39Ar (Argon-Argon) dating technique. Armed with these dates and bolstered by paleomagnetic, paleontological, and sedimentological studies, researchers can place fossils into a dated framework with accuracy and precision. Lucy is dated to just less than 3.18 million years old. == Pseudogenes are found at the same locations in chimp, gorilla, gibbon and man but not on other species. == JonJoe McFadden's "Quantum Evolution" == "Nested hierarchy" refers to the fact organisms are grouped by similarities into successively larger groups -- extremely similar individuals being grouped into species, similar species being grouped into genera, genera into families, families into orders, and so on up to kingdoms. The evolutionary explanation of this pattern is that the similarities that distinguish the groups are the result of branching events in the descent from a common ancestor == Comparisons of the DNA from a wide variety of organisms indicate that this [duplication of genes] is how the globin family of blood proteins evolved over millions of years. This is about the vital red blood pigment hemoglobin that carries the oxygen. It has four polypeptide chains and iron. Evolutionists believe that this evolved from an oxygen-carrying iron-containing protein called myoglobin found in muscles, which has only one polypeptide chain. 1. See D. Batten, Hox (homeobox) Genes-Evolution's Saviour? and D. DeWitt, Hox Hype-Has Macro-evolution Been Proven?. 3. A. Kihm et al., An Abundant Erythroid Protein That Stabilizes Free-haemoglobin, Nature 417(6890):758-763 (13 June 2002); comment by L. Luzzatto and R. Notaro, Haemoglobin's Chaperone, same issue, p. 703-705. 4. See S.E. Aw, The Origin of Life: A Critique of Current Scientific Models, TJ 10(3):300-314, 1996. == Mutations that arise in the homeobox (Hox) family of development-regulating genes in animals can also have complex effects. Hox genes direct where legs, wings, antennae, and body segments should grow. In fruit flies, for instance, the mutation called Antennapedia causes legs to sprout where antennae should grow. == The theory of gravity may not be complete - but that doesn't mean we can't calculate things very precisely using our current theory. The same applies to evolution. We may not be able to know everything about evolution, but current theory is very good at predicting what we should see. == Charles Darwin died on April 19, 1882, at the age of 73. Francis Darwin wrote to Tom Huxley on February 8, 1887, that a report that Charles had renounced evolution on his deathbed was "false and without any kind of foundation," and in 1917 Francis affirmed that he had "no reason whatever to believe that he [his father] ever altered his agnostic point of view." == Publication of four more genomes confirm disputed whole genome duplication theory The publication in Nature this week of four yeast genomic sequences seems to have confirmed the controversial idea, introduced in 1997, that whole genome duplication occurred in Saccharomyces cerevisiae. The very high-coverage sequenceswith virtually no gapsof four species of yeast reveal evidence of tandem gene duplication, segmental duplication (coduplication of tens to hundreds of genes), and whole genome duplication, said study coauthor Giles Fischer, who worked with Bernard Dujon and others at the Centre Nationale de la Recherche Scientifique in France. "One of the major forces that has driven evolution is gene duplication followed by gene loss," Fischer said, "but we did not find only one single mechanism of gene duplication, we found three." http://www.biomedcentral.com/news/20040701/01 "I think that all the mechanisms that we see in this group of species are probably conserved all over the kingdom of life," Fischer said, noting that yeast species are more different from each other than man is from marine invertebrates, fish, birds, and mammals." == Huxley, Thomas H. 1860. "The Origin of Species" in _Darwiniana: Essays by Thomas H. Huxley_, Volume II of the 9-volume series "Collected Essays By T. H. Huxley" (New York: Greenwood Press, Publishers, 1968; originally published in 1893 by Mc Millan & Co.), 475pp., 22-79. Two paragraphs on 58-9: Or, lastly, let us ask ourselves whether any amount of evidence which the nature of our faculties permits us to attain, can justify us in asserting that any phaenomenon is out of the reach of natural causation. To this end it is obviously necessary that we should know all the consequences to which all possible combinations, continued through unlimited time, can give rise. If we knew these, and found none competent to originate species, we should have good ground for denying their origin by natural causation. Till we know them, any hypothesis is better than one which involves us in such miserable presumption. But the hypothesis of special creation is not only a mere specious mask for our ignorance; its existence in Biology marks the youth and imperfection of the science. For what is the history of every science but the history of the elimination of the notion of creative, or other interferences, with the natural order of the phaenomena which are the subject-matter of that science? When Astronomy was young "the morning stars sang together for joy," and the planets were guided in their courses by celestial hands. Now, the harmony of the stars has resolved itself into gravitation according to the inverse squares of the distances, and the orbits of the planets are deducible from the laws of the forces which allow a schoolboy's stone to break a window. The lightning was the angel of the Lord; but it has pleased Providence, in these modern times, that science should make it the humble messenger of man, and we know that every flash that shimmers about the horizon on a summer's evening is determined by ascertainable conditions, and that its direction and brightness might, if our knowledge of these were great enough, have been calculated. == "The _Expression of the Emotions in Man and Animals" by Charles Darwin Man the Tool-maker" by Kenneth P. Oakley == http://www.talkorigins.org/faqs/macroevolution.html What is macroevolution? In evolutionary biology today, macroevolution is used to refer to any evolutionary change at or above the level of species. It means the splitting of a species into two (speciation, or cladogenesis, from the Greek meaning "the origin of a branch") or the change of a species over time into another (anagenesis, not nowadays generally used). Any changes that occur at higher levels, such as the evolution of new families, phyla or genera, is also therefore macroevolution, but the term is not restricted to the origin of those higher taxa. Microevolution refers to any evolutionary change below the level of species, and refers to changes in the frequency within a population or a species of its alleles (alternative genes) and their effects on the form, or phenotype, of organisms that make up that population or species. Another way to state the difference is that macroevolution is between-species evolution of genes and microevolution is within-species evolution of genes. There are various kinds of dynamics of macroevolution. Punctuated equilibrium theory proposes that once species have originated, and adapted to the new ecological niches in which they find themselves, they tend to stay pretty much as they are for the rest of their existence. Phyletic gradualism suggests that species continue to adapt to new challenges over the course of their history. Species selection and species sorting theories claim that there are macroevolutionary processes going on that make it more or less likely that certain species will exist for very long before becoming extinct, in a kind of parallel to what happens to genes in microevolution. The history of the concept of macroevolution In the "modern synthesis" of neo-Darwinism, which developed in the period from 1930 to 1950 with the reconciliation of evolution by natural selection and modern genetics, macroevolution is thought to be the combined effects of microevolutionary processes. In theories proposing "orthogenetic evolution" (literally, straight line evolution), macroevolution is thought to be of a different calibre and process than microevolution. Nobody has been able to make a good case for orthogenesis since the 1950s, especially since the uncovering of molecular genetics between 1952 and the late 1960s. Antievolutionists argue that there has been no proof of macroevolutionary processes. However, synthesists claim that the same processes that cause within-species changes of the frequencies of alleles can be extrapolated to between species changes, so this argument fails unless some mechanism for preventing microevolution causing macroevolution is discovered. Since every step of the process has been demonstrated in genetics and the rest of biology, the argument against macroevolution fails. Non-Darwinian evolutionists think that the processes that cause speciation are of a different kind to those that occur within species. That is, they admit that macroevolution occurs, but think that normal genetic change is restricted by such proposed mechanisms as developmental constraints. This view is associated with the names of Schmalhausen and Waddington, who were often characterised as being non-Darwinians by the modern synthesis theorists. The terms macroevolution and microevolution were first coined in 1927 by the Russian entomologist Iurii Filipchenko (or Philipchenko, depending on the transliteration), in his German-language work Variabilit".8at und Variation, which was the first attempt to reconcile Mendelian genetics and evolution. Filipchenko was an evolutionist, but Darwinism redundant, the so-called "eclipse of Darwinism" (Bowler 1983), he was not a Darwinian, but an orthogeneticist. Moreover Russian biologists of the period had a history of rejecting Darwin's Malthusian mechanism of evolution by competition. In Theodosius Dobzhansky's Genetics and the Origin of Species, he began by saying that "we are compelled at the present level of knowledge reluctantly to put a sign of equality between the mechanisms of macro- and microevolution" (1937, page 12), thereby introducing the terms into the English-speaking biological community (Alexandrov 1994). Dobzhansky had been Filipchenko's student and regarded him as his mentor. In science, it is difficult to deny a major tenet of one's teachers due to filial loyalty, and Dobzhansky, who effectively started the modern Darwinian synthesis with this book, found it disagreeable to have to deny his teacher's views (Burian 1994). The term fell into limited disfavour when it was taken over by such writers as the geneticist Richard Goldschmidt (1940) and the paleontologist Otto Schindewolf to describe their orthogenetic theories. As a result, apart from Dobzhansky, Bernhardt Rensch and Ernst Mayr, very few neo-Darwinian writers used the term, preferring instead to talk of evolution as changes in allele frequencies without mention of the level of the changes (above species level or below). Those who do are generally working within the continental European traditions (as Dobzhansky, Mayr, Rensch, Goldschmidt, and Schindewolf are) and those who don't are generally working within the Anglo-American tradition (such as John Maynard Smith and Richard Dawkins). Hence, the term is sometimes wrongly used as a litmus test of whether the writer is "properly" neo-Darwinian or not (Eldredge 1995: 126-127). The term has been revived by a number of authors such as Stephen Jay Gould and Niles Eldredge, the authors of punctuated equilibrium theory (see Eldredge's 1992 Macroevolutionary Dynamics ), but there is a tendency in these authors to revert to the orthogenetic view that something other than within-species processes are causing macroevolution, although they disavow the orthogenetic view that evolution is progressing anywhere. Conclusion There is no difference between micro- and macroevolution except that genes between species usually diverge, while genes within species usually combine. The same processes that cause within-species evolution are responsible for above-species evolution, except that the processes that cause speciation include things that cannot happen to lesser groups, such as the evolution of different sexual apparatus (because, by definition, once organisms cannot interbreed, they are different species). The idea that the origin of higher taxa, such as genera (canines versus felines, for example), requires something special is based on the misunderstanding of the way in which new phyla (lineages) arise. The two species that are the origin of canines and felines probably differed very little from their common ancestral species and each other. But once they were reproductively isolated from each other, they evolved more and more differences that they shared but the other lineages didn't. This is true of all lineages back to the first eukaryotic (nuclear) cell. Even the changes in the Cambrian explosion are of this kind, although some (eg, Gould 1989) think that the genomes (gene structures) of these early animals were not as tightly regulated as modern animals, and therefore had more freedom to change. == Scientists have surmised that these early hunters must have eventually expanded their food repertoire in order to sustain a growing population, but exactly when they began turning to plants for fuel was scarce. In the new work, Ehud Weiss of Harvard University and his colleagues analyzed plant remains from an archaeological site in Israel called Ohalo II, which dates to 23,000 years ago and includes several huts, hearths and a human grave. Upon excavation, the locality yielded more than 90,000 specimens from 142 plant taxa, including 19,000 well-preserved grass grains. The authors note that the finds not only provide evidence for broad spectrum plant collecting, but also push back the evidence for significant grass collecting 10,000 years earlier than previously had been known. Among the ruins were pieces of acorns, almonds, pistachios, wheat, barley, berries, figs and grapes. Some of the foods were short-lived menu preferences, however. Remains from other sites suggest that by 8,000 years ago, most of the small-grained wild grasses uncovered at Ohalo II were no longer part of the ancient food pyramid. Instead, early humans favored the larger-grained cereal crops, the domestication of which led to the rise of modern agriculture. == Only eukaryotes have mitochondria (and not quite all of them). Prokaryotes lack them. Prokaryotes have no organelles at all, == www.affordablehomepages.com/hovind much good data === Spider aancestors <==o CHELICERATA |-- PYCNOGONIDA `--o EUCHELICERATA `--o MEROSTOMATA |-- XIPHOSURA `--+-- CHASMATASPIDA `--o EURYPTERIDA |-- SCORPIONIDA `-- ARACHNIDA == Bird ancestors DINSAUROMORPHA |--ORNITHISCHIA `--+--SAUROPODOMORPHA | Theropoda |--Herrerasauridae `--+--Ceratosauria `--Tetanurae |--Torvosauroidea `--Avetheropoda |--Carnosauria `--Coelurosauria |--Tyrannosauroidea `--Maniraptora |--Dromaeosauridae | `--AVES In this grouping, almost every alternate name is a terminal taxon, right? What is indicated here is that Aves are coelurosaurs but not tyrannosaurs, maniraptors but not dromaeosaurs, right? They're also theropods of course, and tetanurs, but not herrerasaurs or ceratorsaurs. Neither are they sauropods nor ornithischians, even though they obviously have "bird-hips". Neither Dinosauromorpha, Ornisthichia, Sauropodomorpha nor Theropoda are terminal taxons, but each are clades, right? Theropods and the collective Sauropod group are listed here in sister groups which could be combined into one clade of Sauropodomorpha + Theropoda with Ornithischia as its sister. == Combined fossil reported by Nat Geo. The tail half was later designated as the holotype for _Microraptor zhaoianus_, and the front half was referred to the bird _Yanornis_ === So there is a lot of philosophical hay to be made from evolution. It is not, I think, a "system" in the older sense - there are no overriding morals or doctrines. It is largely a technical philosophy, answering a number of the long-standing problems that bedevilled the traditional classical philosophies - the problem of change. Not all of it derives from Darwin, although I happen to agree with Ghiselin that Darwin was perhaps the most original philosopher since Ockham. But it all comes together in a radical revision of the ways of thought we inherited from the middle ages and renaissance. Now I know that people blame evolution for all ills but it seems to me that what goes by the name of "evolutionary" philosophy, such as Spencer's and Haeckel's philosophical musings, are in fact an amalgam of oldthink and newthink. In point of fact, there has been until fairly recently very little actual *evolutionary* philosophy (beginning with Ghiselin's _Triumph of the Darwinian Method_ in 1969, and Hull's and Beckner's earlier work; say, beginning at the centenary of the Origin). John Wilkins == Macroevolution as it's defined by scientists http://www.talkorigins.org/faqs/macroevolution.html http://www.nhm.ac.uk/hosted_sites/paleonet/paleo21/mevolution.html is also observed to occur [observed speciations], http://www.talkorigins.org/faqs/faq-speciation.html http://www.talkorigins.org/faqs/speciation.html http://www.talkorigins.org/faqs/evolution-research.html http://www.talkorigins.org/faqs/comdesc/ http://www.talkorigins.org/faqs/faq-transitional.html http://tolweb.org/tree?group=life http://www.ucmp.berkeley.edu/historyoflife/histoflife.html http://www.ucmp.berkeley.edu/alllife/threedomains.html http://www.ucmp.berkeley.edu/alllife/eukaryotasy.html == The Map That Changed the World: William Smith and the Birth of Modern Geology ISBN: 0060931809 The first geology map of England. == However, we know that over time either man-driven selection or natural selection makes distinctions within the kind, so that they are no longer physically able to reproduce, such as populations of Anableps(fish) with left handed gonopodiums and right handed gonopodiums with their respective females cannot interbreed physically any more Corydoras has about 150 species and subspecies, and the genus has all manner of interesting biological oddities, such as mimicry, symbiosis, etc, appearing among its ranks. It is one of the most common genera of fish over the whole of Amazonia and covers also the bulk of south America. Its armoured plates make it the ideal subject for fossilisation. How many fossilised species are there? One. Corydoras revelatus. It is the only Cory fossil in existence, and yet it is an almost perfect fossil. Why are there no more? Do they interbreed? No they don't, == Ten Tiny Fossils, First Evidence of Bilaterian Structure, Predate Cambrian Explosion Part of the story of the evolution of life forms from one-celled organisms to animals with symmetrical, bilateral body plans is written into 10 smaller-than-supposed fossils found in southwestern China and documented in last week's issue of the journal Science. Researchers assert that the fossils--sporting nature's prevailing bilateral body architecture, and dated to between 580 million and 600 million years old--represent evidence of the oldest animals ever found. Their assigned age is greater by some 50 million years than the "Cambrian Explosion," during which most major groups of animals start appearing in the fossil record. There had been some controversial molecular evidence suggesting bilateral precursors to the Cambrian Period, but nothing conclusive had been found. Study co-author David Bottjer of the University of Southern California said that not only did the animals these fossils represent precede the Cambrian Period, they also had evolved "a good bit." Each of the creatures featured a mouth and an anus, and each had two pits that Bottjer thinks must have sensed environmental change, such as light and darkness. Bottjer's find synched up nicely with a report in April from Dartmouth biologist Kevin Peterson, according to the San Francisco Chronicle. Writing in the Proceedings of the National Academy of Sciences, Bottjer wrote that a "molecular clock" he had devised to measure average rates of mutation among fossils and their descendants would date the first bilaterians at 573 million to 656 million years old. In the "Cambrian Explosion" story of biology textbook fame, a slew of creatures sporting an array of anatomical blueprints burst onto the scene, or at least into the fossil record, around 540 million years ago. The back story is more muddled, with few fossils to document the evolution of one- celled organisms into the much more architecturally advanced Cambrian creatures. And of particular relevance to human anatomy is the question of how animals with a two-sided, or bilateral, body plan arose. According to a new study published yesterday in the online edition of the journal Science, 10 tiny fossils from southwestern China may represent the oldest evidence yet for this bilateral body plan - the same general blueprint later embellished upon by everything from humans to clams. The fossils, shaped like flattened turtle shells but no bigger than a speck to the unaided eye, were discovered in China's Guizhou Province and dated to between 580 million and 600 million years in age. Among the creature's purported anatomical features, researchers have identified a mouth, a pharynx, a digestive tract containing a large stomach or intestine, and a pair of all-purpose body cavities. Molecular evidence suggests that bilateral architecture existed before the Cambrian Period's "explosion" of variable life forms, but no conclusive evidence had been unearthed. The newly identified fossils, named Vernanimalcula guizhouena, may up the ante in the debate by implying that creatures with these blueprints not only preceded the Cambrian by millions of years, but also had undergone "a good bit of evolution" to boot, said study co-author David Bottjer, a professor of earth sciences at the University of Southern California. "I think it's a pretty nifty discovery," said Doug Erwin, a paleontologist at the National Museum of Natural History in Washington, D.C., who wasn't involved in the research. The surprise, he said, is "probably because this is a much smaller beast than I think many people had been expecting." The tiny creatures have attracted a fair bit of controversy, however. Some paleontologists, Erwin said, have expressed doubts as to whether the purported Chinese fossils really represent bilateral life- forms, or whether they represent life-forms at all. But Erwin said the numerous pictures he's seen have helped convince him of their authenticity. "The more similar examples that you see of something like this, the more confident you are that it's a biological structure," he said. "In this case, I'm reasonably confident that it's real." Despite the controversy, the tiny fossils may have prompted those searching for pre-Cambrian signs of life to think in smaller terms, Bottjer said. "Certainly, it says, look around for small stuff and you might be surprised what you find," he said. == Book Of Life, edited by Gould. == the phylum Bryozoa didn't originate in the Cambrian, but rather the Ordovician == Asexual reproduction results in just more of the same. An evolutionary condom of sorts. Sexual reproduction increases the gene pool from which all variation and modifications are born, resulting in new species (i.e) new forms of life that are better adapted to their respective environments. Environments which CHANGE with time. Without sexual reproduction, there would be no "plasticity" and very little if any diversity in the flora and fauna of this planet. Sex started a long time before anyone thought up 'organs.' In the most general manner, sex started when two ameoba-type organisms fused, rather than splitting. Fusing their genetic material proved beneficial (for whatever reasons, parasites being the popular one at the moment), so selection pressure encouraged fusing behavior until a large percentage of all reproduction takes the form of "two into one" rather than the earlier "one into two." There's not a great deal of direct evidence for any of this, but there does exist a type of reproduction somewhere between assexual and "true" sexual. Some organisms (IIRC, mosses for example) are homogamous, in that the reproductive cells from each donor is identical. It takes two gametes to procreate, but they haven't yet evolved "gender." From that system, any imbalance of donated resources will lead, by positive feedback, to the egg-sperm dynamic we see today. If one partner of a homogamous coupling skimps on the size of their donated cell, they have the resources to make more. The smaller, the better (for them). This leads to sperm. They do, however, run the risk of fusing with another proto-sperm, in which case there aren't enough total resources for the new zygote to develop and the whole investment is wasted. Other individuals, rather than running that risk, pad their own gamete with extra nutrients, so it can survive whether it meets a regular gamete or a "cheater" gamete. Over time, those specialize into eggs. After all that, it's just a matter of tinkering with various delivery systems. By the time you get to actual "anatomy", sex is old hat. == Japanese-Led Team Compares Chimp, Human Chromosomes Chimpanzees may be our closest relatives, but the fairly meager genetic divide is marked by some surprising distinctions that account for differences in cognition and susceptibility to disease, among other things. That's the conclusion reached by a team of international researchers who mapped genes within the chimp's No. 22 chromosome pair, then compared it to its human analogue, No. 21--more than 98 percent of DNA found on chimp 22 shows up on human 21. Hoping to glean a better understanding of human evolution and the history of genetic diseases, hundreds of geneticists and technicians spread throughout five countries worked together on the study and published their results in last week's issue of the journal Nature. The researchers assiduously sequenced the 33.3 million base pairs of DNA found in chimp chromosome 22, then compared the lineup with that of human 21. What they found surprised them: Some 70,000 sections of DNA were different in chimp 22 than in human 21, and in both species, long stretches of DNA had been lost or added over time. All of those changes make for a very complex and intriguing puzzle that scientists will piece together gradually in order to better explain the divergence of chimp and human evolutionary tracks. On the way: American researchers later this year will will write up their comparison of the human and chimp genomes. An international team of scientists, seeking to track the course of human evolution and the ancient roots of genetic diseases, has completed the first highly accurate map of the genes in a single chimpanzee chromosome and compared them gene-by-gene with their human counterparts. The result, the scientists say, reveals surprising differences between the species, even though they are the closest of relatives in the primate family. The international team completed the first sequence of the genes in chimp chromosome pair No. 22, one of 24 chromosome pairs in the chimpanzee. That pairs the counterpart of chromosome 21 in the human array of 23 chromosome pairs. The sequencing feat was accomplished by a consortium of scientists working at genetics centers in five nations headed by Yoshiyuki Sakaki and Asao Fujiyama of Japan's Genomics Sciences Center in Yokohama. The group's report, with 45 co-authors representing hundreds of geneticists and technicians, is being published today in the scientific journal Nature. Within a month or two, an American research consortium is expected to announce completion of the most accurate map of the entire chimp genome. Chimp chromosome 22 contains 33.3 million chemical DNA units, known as bases. The report describes how they painstakingly determined the sequences of the DNA units with accuracy better than 99.99 percent. As the team compared the chimp DNA with the genetic material in human chromosome 21, the scientists found to their surprise that both species had both gained and lost thousands of stretches of DNA, although what caused those changes and what effect they might have had remain a mystery, they said. Much of the work's value lies in providing clues to the nature and timing of the divergent evolution of the chimp and human lineages, according to Robert Waterston of the University of Washington, a leader in the completion of the Human Genome Project. Despite their close relationship, chimps and humans vary greatly in their susceptibility to diseases and in their cognitive and language skills. The answers to when and how those differences arose should lie in the changes in their genes. The chimp gene group was particularly interested in this chromosome, Sasaki said, because an extra copy of the human analogue, chromosome 21, is the cause of Down syndrome. Symptoms of Down syndrome have been reported in chimps, too == Star and planet formation We've seen evidence from these observations with Spitzer that there are ices and simple organic compounds such as methanol in these discs," says Boss. "The UV (ultraviolet) flux in addition, if it's in a disc (in a star-forming region), could perhaps convert these ices into more advanced organic compounds such as polycyclic aromatic hydrocarbons." Polycyclic aromatic hydrocarbons (PAHs) are the building blocks for more complex organic molecules, and they appear to be widespread throughout the universe. PAHs may have played a vital role in the origin of life on Earth. "Even amino acids - alanine and guanine - can form, as has been shown by laboratory studies, by UV irradiation of simple ices," adds Boss. "So one can imagine a system where the formation of life-bearing elements is hastened along by pre-biotic chemistry that occurs in the disc, even before things start getting going on a habitable planet." == Icy birth? Amino acids form in simulations of space ice - In another step toward understanding the origin of Earth's biological molecules, two independent laboratory experiments have produced amino acids--the building blocks of proteins--by simulating conditions in icy, interstellar space. The results, published in the March 28 Nature, suggest that some amino acids could have formed in giant clouds of icy particles and then hitched rides on comets and asteroids to planets throughout the universe. In the search for precursors to life on Earth, various researchers have created amino acids and other organic molecules in lab experiments that simulate specific environments, such as those on early Earth or asteroids. Researchers have also speculated that amino acids might form on interstellar ice particles that are exposed to ultraviolet light, yet until now, no one had shown that this could actually happen, says Bernstein. "I think it's a really exciting justification of the notion that these building blocks can come from outer space. In each of the new experiments, performed at very low temperatures and pressures, scientists chose small molecules found in space and deposited them on a surface while irradiating them with ultraviolet light. Chemists made an icy layer of water, methanol, ammonia, and hydrogen cyanide. The other team, which includes scientists from four European institutions, used less water than the NASA team did. It also included carbon monoxide and carbon dioxide in its mix but no hydrogen cyanide. After warming the samples to room temperature, the NASA group detected three amino acids: glycine, alanine, and serine. The European group identified 16 amino acids, including 6 that appear in life's proteins. The creation of amino acids in the European group's experiment was a surprise. The team had been preparing interplanetary ice samples to test equipment for the upcoming Rosetta space probe, which will analyze a comet's chemistry. To rule out contamination by natural amino acids, both research teams used a heavy isotope of carbon in their initial chemicals and found that same isotope in the final amino acids. Moreover, some amino acids have both a left- and a right-handed form, but living organisms contain almost exclusively the left-handed variety. So, most amino acids on Earth are in that form. The researchers produced a 50-50 mix of left-handed and right-handed forms in their samples, a confirmation that the amino acids derived from the experiment. These studies may help explain how some amino acids formed initially, but they do not indicate why life incorporates only left-handed amino acids. One popular theory is that certain naturally occur ring forms of UV radiation, called circularly polarized light, preferentially produce left-handed varieties in interstellar space. By running their experiments again with such UV light, the NASA group is now pursuing this possibility. Another question is, How long can such amino acids survive in their icy birthplaces? "Really rich, robust chemistry taking place in the cosmos" contributes to making the molecules necessary for life. Interstellar ice chemistry is just one of many processes--including chemical reactions on asteroids or the early Earth--that could form amino acids. == Some butterflies are indeed poisonous and birds learn not to eat them. Some other butterflies (called "mimics") aren't actually poisonous, but they mimic the appearance of the poisonous ones to avoid predators. === Jumping genes, aka retrotransposons, are bits of genetic material that copy themselves and move around in creatures' genomes. They have the potential to disrupt the genes they "land" in and are thought to contribute to the gradual --and perhaps the occasional major -- genetic shifts that drive evolution. While organisms like yeast have just a few dozen jumping genes in their genomes, mammals' genomes contain hundreds of thousands of copies of their jumping genes' DNA, making it difficult to know where or when -- or even if -- a jump has happened. == Bipedality in Chimpanzee (Pan troglodytes) and Bonobo (Pan paniscus): Testing Hypotheses on the Evolution of Bipedalism Elaine N. Videan and W.C. McGrew == It's frequently thought that hoatzins are related to cuckoos, or to tauracos, but so far all attempts to show that have failed. Even the most recent one (Hughes, J. M., and A. J. Baker. 1999. Phylogenetic relationships of the enigmatic hoatzin (Opisthocomus hoazin) resolved using mitochondrial and nuclear gene sequences. Mol. Biol. Evol. 16:1300-1307.) has recently been shown to rely on sequencing errors for its conclusions. No properly scored sequence data has yet been able to attach hoatzins to anything. == If you believe that Hitler was an evolutionist, check out chapter 5 of Mein Kampf. == Richard Dawkins' *1976* book _The Selfish Gene_ and his *1982* _The Extended Phenotype_ and the *extensive* scientific debate on the issue of what is the fundamental unit (or units) of selection. Gould spends at least 150 pages on the issue in his 2002 book _The Structure of Evolutionary Theory_. == The human evolutionary line and chicken lines went their separate ways 300 million years ago, while the human and fish lines seperated more than 400 million years ago. == There are quite a few predictions that would falsify particular models of evolution. Rabbit fossils in the Cambrian would put paid to current models of common descent quite nicely. So would birds with mammary glands, or three bones in the middle ear. So would plants with cytochrome-c more similar to that of humans than that of monkeys. == What two animals need fleas to survive? The hedgehog and the armadillo, which require flea activity to stimulate their skin, may be the only creatures grateful for fleas. Deloused armadillos and hedgehogs do not live very long. == Regarding macroevolution: http://www.talkorigins.org/faqs/comdesc/ Regarding irreducible complexity: http://www.talkorigins.org/faqs/behe.html http://www.millerandlevine.com/km/evol/DI/clot/Clotting.html === Cambrian Explosion 1995 issue of _Time_, "When Life Exploded," pages 66-74. == Very similar genes and proteins (or pseudogenes, or endogenous retrovirii) require some explanationin terms of copying from a common source. == Life origins http://www.ucmp.berkeley.edu/education/events/eukevol1.html http://www.sciencedaily.com/releases/2002/02/020207075601.htm http://www.pnas.org/cgi/reprint/93/1/166.pdf http://www.biomedcentral.com/1471-2148/3/14 http://www.denovobio.com/pdf/deNovoBiologic.pdf http://dekalb.dc.peachnet.edu/~pgore/students/w96/joshbond/symb.htm http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_ui ds=9608053&dopt=Abstract This gives a list of journal references for prokaryote to eukaryote evolution: http://spot.colorado.edu/~perkinss/teaching/EME/Eukmicrobesrefs.pdf == Schlichting, C. D. and M. Pigliucci (1998). Phenotypic Evolution: A Reaction Norm Perspective. Sunderland, MA, Sinauer Associates. 1970 _Populations, Species, and Evolution_, 1982 _The Growth of Biological Knowledge_. == talkorigins [Q.] I thought evolution was just a theory. Why do you call it a fact? [A.] The phenomena of biological evolution are changes in the heritable characteristics of populations over time. That these occur is a fact. Biological evolution refers to the common descent of all living organisms from shared ancestors. The evidence for this historical evolution -- genetic, fossil, anatomical, etc. -- is so overwhelming that it is also considered a fact. The theory of evolution describes the mechanisms that cause evolution. So evolution refers to both fact and theory. [U.] http://www.talkorigins.org/faqs/evolution-fact.html http://www.talkorigins.org/faqs/faq-intro-to-biology.html http://www.talkorigins.org/faqs/faq-misconceptions.html#proof [Q.] Don't you have to be an atheist to accept evolution? [A.] No. Many people of Christian and other faiths accept evolution as the scientific explanation for biodiversity. [U.] http://www.talkorigins.org/faqs/faq-god.html http://www.talkorigins.org/faqs/interpretations.html [Q.] Isn't evolution just an unfalsifiable tautology? [A.] No. Evolutionary theory is in exactly the same condition as any other valid scientific theory, and many criticisms of it that rely on philosophy are misguided. [U.] http://www.talkorigins.org/faqs/evolphil.html [Q.] If evolution is true, then why are there so many gaps in the fossil record? Shouldn't there be more transitional fossils? [A.] Due to the rarity of preservation and the likelihood that speciation occurs in small populations during geologically short periods of time, transitions between species are uncommon in the fossil record. Transitions at higher taxonomic levels, however, are abundant. [U.] http://www.talkorigins.org/faqs/faq-transitional.html http://www.talkorigins.org/faqs/fossil-hominids.html http://www.talkorigins.org/faqs/punc-eq.html http://www.talkorigins.org/origins/postmonth/feb98.html [Q.] No one has ever directly observed evolution happening, so how do you know it's true? [A.] Evolution has been observed, both directly and indirectly. It is true. [U.] http://www.talkorigins.org/faqs/faq-misconceptions.html#observe http://www.talkorigins.org/faqs/comdesc/ [Q.] Then why has no one ever seen a new species appear? [A.] Speciation has been observed both in the laboratory and in nature. [U.] http://www.talkorigins.org/faqs/faq-speciation.html http://www.talkorigins.org/faqs/speciation.html [Q.] Doesn't the perfection of the human body prove Creation? [A.] No. In fact, humans (and other animals) have many suboptimal characteristics. [U.] http://www.talkorigins.org/faqs/jury-rigged.html [Q.] According to evolution, the diversity of life is a result of chance occurrence. Doesn't that make evolution wildly improbable? [A.] Evolution is not simply a result of random chance. It is also a result of non-random selection. [U.] http://www.talkorigins.org/faqs/chance.html http://www.talkorigins.org/faqs/faq-misconceptions.html#chance [Q.] Doesn't evolution violate the second law of thermodynamics? After all, order cannot come from disorder. [A.] Evolution does not violate the second law of thermodynamics. Order emerges from disorder all the time. Snowflakes form, trees grow, and embryos develop, etc. [U.] http://www.talkorigins.org/faqs/thermo.html http://www.talkorigins.org/faqs/faq-misconceptions.html#thermo [Q.] Didn't Darwin renounce evolution on his deathbed? [A.] The Darwin deathbed story is false. And in any case, it is irrelevant. A scientific theory stands or falls according to how well it is supported by the facts, not according to who believes it. [U.] http://www.talkorigins.org/faqs/hope.html [Q.] Where can I learn more about evolution? [A.] You might start with the talk.origins FAQs. If, however, you want a deeper understanding of evolution, a library would be a more appropriate place to look. The FAQs listed below provide some good references. [U.] http://www.talkorigins.org/faqs/reading-list.html http://www.talkorigins.org/faqs/faq-intro-to-biology.html http://www.talkorigins.org/faqs/evolution-definition.html [Q.] How do you know the earth is really old? Lots of evidence says it's young. [A.] According to numerous, independent dating methods, the earth is known to be approximately 4.5 billion years old. Most young-earth arguments rely on inappropriate extrapolations from a few carefully selected and often erroneous data points. [U.] http://www.talkorigins.org/faqs/faq-age-of-earth.html http://www.talkorigins.org/origins/faqs-youngearth.html [Q.] But radiometric dating methods rely on the assumptions of non- contamination and constant rates of decay. What if these assumptions are wrong? [A.] Isochron dating techniques reveal whether contamination has occurred, while numerous theoretical calculations, experiments, and astronomical observations support the notion that decay rates are constant. [U.] http://www.talkorigins.org/faqs/isochron-dating.html http://www.talkorigins.org/faqs/faq-age-of-earth.html [Q.] I heard that the speed of light has changed a lot. This means that light from galaxies billions of light years away might not be billions of years old. Is this true? [A.] Barry Setterfield's hypothesis of a decaying speed of light was based on flawed extrapolations from inaccurate measurements, many of which were taken hundreds of years ago. [U.] http://www.talkorigins.org/faqs/c-decay.html [Q.] If the Earth is so old, doesn't that mean the Earth's decaying magnetic field would have been unacceptably high at one time? [A.] No. The Earth's magnetic field is known to have varied in intensity and reversed in polarity numerous times throughout the planet's history. [U.] http://www.talkorigins.org/faqs/magfields.html [Q.] Isn't the fossil record a result of the global flood described in the Book of Genesis? [A.] No. A global flood cannot explain the sorting of fossils observed in the geological record. This was recognized even prior to the proposal of evolutionary theory. [U.] http://www.talkorigins.org/faqs/faq-noahs-ark.html http://www.talkorigins.org/origins/postmonth/apr02.html [Q.] What about those fossils that cut through multiple layers? [A.] They have natural explanations: tree-roots that grew into soft, underlying layers of clay, and fossils found in inclined strata. They can also be observed forming in modern environments. [U.] http://www.talkorigins.org/faqs/polystrate.html [Q.] What about those human footprints that appear next to dinosaur footprints? [A.] The man-tracks of the Paluxy Riverbed in Glen Rose, Texas were not man tracks at all. Some were eroded dinosaur tracks, and others were human carvings. [U.] http://www.talkorigins.org/faqs/paluxy.html [Q.] Didn't they find Noah's Ark? I saw something on TV about this. [A.] The producers of America's 1993 CBS television show, The Incredible Discovery of Noah's Ark, were hoaxed. Other ark discovery claims have not been substantiated. [U.] http://www.talkorigins.org/faqs/ark-hoax.html [Q.] The odds against a simple cell coming into being without divine intervention are staggering. [A.] And irrelevant. Scientists don't claim that modern cells came into being through random processes. They are thought to have evolved from more primitive precursors. [U.] http://www.talkorigins.org/faqs/abioprob/ [Q.] Creationists are qualified and honest scientists. How can they be wrong? [A.] The quality of an argument is not determined by the credentials of its author. Even if it was, a number of well-known creationists have questionable credentials. Furthermore, many creationists have engaged in dishonest tactics like quoting out of context or making up references. [U.] http://www.talkorigins.org/faqs/credentials.html http://www.talkorigins.org/origins/faqs-creationists.html http://www.talkorigins.org/faqs/quotes/ http://www.talkorigins.org/faqs/homs/misquotes.html [Q.] What about Immanuel Velikovsky? Didn't he show that the Earth has experienced a lot of major catastrophes? [A.] No, he simply claimed that certain written legends must have described real events. [U.] http://www.talkorigins.org/origins/faqs-catastrophism.html http://www.talkorigins.org/faqs/faq-velikovsky.html [Q.] Where can I find more material on the Creation/Evolution debate? [A.] Contact the National Center for Science Education, or see the TalkOrigins Archive and its Other links page. [U.] http://www.NatCenSciEd.org/ http://www.talkorigins.org/faqs/reading-list.html http://www.talkorigins.org/faqs/organizations.html http://www.talkorigins.org/origins/other-links.html [Q.] What about intelligent design? [A.] Intelligent design advocates often use the very same arguments that the young-earth creationists have used in the past. The Archive does have some FAQs on Behe's irreducible complexity, Jonathan Wells's icons of evolution, and Dembski's specified complexity (see questions below). Further essays on intelligent design can be found on our sister site, TalkDesign, and also at the TalkReason site. [U.] http://www.talkdesign.org http://www.talkreason.org http://www.talkdesign.org/faqs/hunch/hunch.html [Q.] Doesn't irreducible complexity (as described in Behe's _Darwin's Black Box_) shown that some biomechanical systems could not evolve gradually, but must have all their parts created at once? [A.] Behe's irreducible complexity considers only an unrealistically simplistic model of evolution. Evolutionary mechanisms that Behe doesn't consider, such as functional change and coevolution, make irreducible complexity not only possible, but expected. [U.] http://www.talkorigins.org/faqs/behe.html http://www.talkdesign.org/faqs/icdmyst/ICDmyst.html [Q.] Hasn't Jonathan Wells shown that Darwinist claims about such icons of evolution as the peppered moth, Haeckel's embryos, and Darwin's finches have been disproven? If so, why are these claims still found in biology textbooks? [A.] Scientists _have_ been complaining for decades about the poor quality of science instruction in school and about the content of science textbooks. However, Dr. Wells's arguments include many false statements, many misunderstandings of the science involved, and many misunderstandings of the significance of the subjects that he pontificates on. [U.] http://www.talkorigins.org/faqs/wells/ http://www.ncseweb.org/pdf/QRBreview.pdf [Q.] Doesn't William Dembski's specified complexity mean that an intelligent designer had to be responsible for the observed complexity and diversity of living things? [A.] The sophistication of Dembski's arguments is superficial. One of the most thorough examinations of Dembski's ideas is available on the Archive. [U.] http://www.talkorigins.org/design/faqs/nfl/ http://www.talkdesign.org/faqs/present_arguments.html http://www.talkdesign.org/faqs/demskiscompass.html http://www.antievolution.org/people/dembski_wa/ [Q.] Isn't it true that scientists are abandoning evolution? [A.] That is not even remotely true. [U.] http://home.entouch.net/dmd/moreandmore.htm [offsite] http://www.talkorigins.org/faqs/steve/ http://www.talkorigins.org/faqs/edwards-v-aguillard/amicus1.html [Q.] If evolution is true, why don't you take Dr. Kent Hovind's $250,000 challenge and make yourself rich? [A.] Kent Hovind's $250,000 challenge is a propaganda ploy and nothing more, rather like the doctorate Hovind claims from Patriot University. [U.] http://www.talkorigins.org/faqs/hovind/ [Q.] Don't you know that the earth is round? [A.] Yes, we do. We keep a copy of the International Flat Earth Society flyer here to document that real people in modern times do assert that the earth is flat, not because *we* think the earth is flat. [U.] http://www.talkorigins.org/faqs/flatearth.html [Q.] Isn't the TalkOrigins Archive just some website that has no particular credibility? Those FAQs and essays aren't peer- reviewed, and many are written by interested laymen rather than specialists, so they can be ignored, right? [A.] We encourage readers not to take our word on the issues, but rather to look at the primary literature and evaluate the evidence. While materials on the Archive have not necessarily been subjected to formal peer-review, many have been subjected to several cycles of commentary in the newsgroup prior to being added to the Archive. Most of our materials provide links and/or bibliographic references to enable the reader to evaluate the evidence for themselves. While anyone can decide to ignore our materials, the Archive has been recognized as a valuable online resource by many well-known groups, magazines, and individuals. Further, a number of college courses have chosen to use materials from the Archive in their coursework. [U.] http://www.talkorigins.org/faqs/awards/ USING THE WORLD WIDE WEB TO ACCESS FAQS The World Wide Web is the method for accessing the TalkOrigins Archive. The WWW Uniform Resource Locator (URL) for the talk.origins FAQ archive is: http://www.talkorigins.org/ The Archive is updated frequently and contains numerous features, including links to other creation/evolution web pages, archives of user feedback, selected posts from talk.origins, a chat facility, and a powerful search engine. RECENT EVENTS transferred over 15 gigabytes of data. Determining Distances to Astronomical Objects. Astronomers can measure distances to objects in the universe whose light took thousands, millions, or even billions of years for their light to reach us. This has obvious implications for those who believe the universe is under distances to various types of astronomical objects and how young-earth creationists deal with large astronomical distances. http://www.talkorigins.org/indexcc/index.html An Index to Creationist Claims. A collection of creationist claims which aims to be comprehensive. It includes brief rebuttals and, in many cases, pointers to more information. This resource replaces the anti-creationism FAQ by Jim Meritt. POST OF THE MONTH Each month, a post to the talk.origins newsgroup that either shows rare brilliance, wit or insight, or that exemplifies what the newsgroup is all about, is selected as the TalkOrigins Archive's Post of the Month. Nominations can be made throughout the month, and at the end of each month, a vote is held to determine the winner. To nominate a post, reply to it on the newsgroup changing the subject to include the phrase POTM nomination or Post of the Month nomination. Any contributor to talk.origins may nominate or vote for a post; nominations are accepted if they are seconded by at least one other poster. Past winners may be viewed at http://www.talkorigins.org/origins/postmonth/ REQUEST FOR FAQS (RFF) While talk.origins already has a slew of FAQs, there are several issues that come up regularly or semi-regularly on the newsgroup that aren't adequately addressed by the existing set of FAQs at the TalkOrigins Archive. So, the Archive now maintains a Request For FAQs (RFF) list, which describes potential topics for future FAQs. People wishing to write FAQs may check the RFF list below, see if their knowledge or expertise matches one of the FAQ openings, and, if so, start pounding away at the keyboard. The list is available at http://www.talkorigins.org/origins/faqs-rff.html The global flood: Hydrological sorting as an explanation for the fossil record Ecological zonation as an explanation for the fossil record Differential mobility as an explanation for the fossil record Fine-grained fossil sorting by subtle details Architectural analysis: Could the Ark have been made seaworthy? Lack of evidence of pre-flood human civilizations Lack of evidence for global flood in ancient historical records Rapid deposition of layered sediments (Mt. St. Helens, for example) Source of the flood: Subterranean reservoirs Source of the flood: Runaway subduction Source of the flood: Comet impact Where did the flood waters go? Fragile/soluble items preserved in supposedly flood-deposited strata Non-sedimentary rocks in supposedly flood-deposited strata Glacial evidence in supposedly flood-deposited strata Volcanic and impact bolide evidence in supposedly flood-deposited strata Large local floods (e.g., Channeled Scablands) Fossil horizons/extinction events Paleosols and hardgrounds The fall of the deluge as a scientific theory Age of the earth/universe: Spiral galaxy formation/density waves Comets and the Oort Cloud/Kuiper Belt The population growth argument Tidal rhythmites Coral reef growth rates/coral clocks Varves as a dating technique Correlations of different dating methods Values of the Hubble constant Radiocarbon dating Radioactive dating 'anomalies' Tidally locked astronomical systems The Oklo reactor White dwarf cooling rates Dendrochronology Concordia/discordia dating General cosmology, astronomy and physics: Evidence for the Big Bang Determining distances to astronomical objects Constancy of physical constants/change in alpha Origin of the Earth/solar system Origin of the Moon The anthropic principle Stellar evolution and classification Galactic evolution and classification Dark matter Dark energy/quintessence Large-scale structure of the universe Quantized redshifts Halton Arp's anomalous redshifts The ultimate fate of the universe Supernova 1987A The real debates in evolution: The origin of sex Evolutionary psychology How important are neutral mutations? Haldane's dilemma Evolution of language Evolution of intelligence in humans General geology and paleontology: Plate tectonics/continental drift Paleoclimatology Ice Ages Snowball Earth The geologic time scale Major and minor extinctions Taphonomy Stratigraphic succession What caused the extinction of the dinosaurs? Protoavis 'Out of place' fossils Non-vertebrate animal transitional fossils Plant transitional fossils Specific in-depth coverage of any transitional series Theology: Ancient Christians who accept evolution and an old earth Modern Christians who accept evolution and an old earth Symbolic views of Genesis Creationism and racism (Hamitic hypothesis) The flat-earth and geocentrist movements Omphalos/the 'appearance of age' argument Genetics/molecular biology/chemistry: Shared pseudogenes between humans and other primates Degrees of genetic similarity between humans and other primates Chromosomal homology between humans and other primates A comprehensive list of beneficial mutations Information-increasing mutations The RNA World Molecular phylogeny General evolution: Fluctuating selection vs. sustained long-term selection Ring species The evolution of dog breeds Evolution of other domesticated animals Cladistics Feathered dinosaurs Ontogeny recapitulates phylogeny: disproved Vestigial structures and atavisms Comparative anatomy and homology Living fossils Evolution of the flagellum Evolution of any complex structure The Cambrian explosion Biogeography Developmental biology (evo-devo) Is Homo erectus just a modern human? Miscellaneous: The young-earth chronology: Bishop Ussher's timescale Tierra Richard Dawkins' Methinks it is like a weasel program Genetic algorithms Biographies of prominent figures in the evolution-creationism debate Creationist responses to terrorism The Scopes Trial Creationist demographics Creationist political/school-board activity The Santorum Amendment Local pro-science advocacy organizations Book reviews: Dean Kenyon's Of Pandas and People Phillip Johnson's Darwin on Trial Hugh Ross's The Creator and the Cosmos === Both one and three-toed Dinohippus fossils have been found in the same geologic layer (Ashfall Fossil Beds in northeastern Nebraska), and that this indicates that they were living together at the same time in North America? == Palaeontological documentation of speciation in Cenozoic molluscs from Turkana Basin The phylogenetic geometry of molluscan lineages from the Turkana Basin sequence clearly conforms to the punctuated equilibrium model Gould == Rieseberg was able to show that one sunflower species, Heilanthus anomalus, results from an ancient, natural hybridization of two other, older species. Remarkably, Rieseberg has been able to replicate this hybridization under controlled conditions, in effect, reproducibly re-enacting the creation of a new species. On a bit longer time scale, we have the evidence that all the various cichlids of the rift lakes in Africa evolved within 200,000 years. But even closer in time, we have: Recent paleoclimatological data from Thomas C. Tohnson of the University of Minnesota and his colleagues point to an even more restricted window for the origin of the Victoria cichlid flock: the lake seems to have dried out almost completely less than 14,000 years ago. No more than a small fraction of individual cichlids, let alone species, could have survived such an ordeal. In that case, the speciation rate exhibited by its cichlids is truly remarkable, being unmatched by other vertebrates. In addition, Lake Nabugabo, a small body of water separated from Lake Victoria by a sandbar that is no more than 4,000 years old, contains five endemic species of cichlids. These fishes are believed to have close relatives in Lake Victoria, which differ from the former mainly in the breeding coloration of the males. Even more remarkably, it turns out that the southern end of Lake Malawi was dry only two centuries ago. Yet it is now inhabited by numerous species and color morphs that are found nowhere else. These examples, bolstered by recent DNA data from Lake Tanganyika, suggest a mechanism for the speciation of cichlids: repeated isolation. It appears that successive drops in the level of Lake Tanganyika, by as much as 2,000 feet, facilitated the formation of Tropheus color morphs and all the other rock-dwelling cichlids. Populations that used to exchange genes instead became isolated in small pockets of water. They developed independently, coming into contact once again as the water level rosebut could no longer interbreed. Such repeated isolation, which is a frequent factor for 'freshwater' fishes, since spread outside a watershed is difficult, may well be the reason why freshwater environments are so species rich. Like the tropics, there are many local 'islands'. == The latest word on the evolution of Dionaea and Aldrovanda Cameron KM, Wurdack KJ, Jobson RW. (2002). Molecular evidence for the common origin of snap-traps among carnivorous plants. American Journal of Botany 89:1503-1509. confirms Darwin's original view: Darwin, Charles. Insectivorous Plants (New York: D. Appleton & Co., 1875. [first published London: John Murray, 1875]) Insectivorous Plants online, pp 355-6, 360. http://pages.britishlibrary.net/charles.darwin3/insectivorous/insect_fm.htm And don't miss Makoto Honda's carnivorous plants web site: Honda M. (2001). Insectivorous Plants in the Wilderness. http://www.honda-e.com/default.htm 4. Hines W. (2002). Hemoglobin and Irreducible Complexity. Talk.origins post. 5. Thornhill RH, Ussery DW (2000). A classification of possible routes of Darwinian evolution. http://www.talkdesign.org/faqs/icdmyst/ICDmyst.html 7. Miller K. (2000). The Evolution of Vertebrate Blood Clotting. http://www.millerandlevine.com/km/evol/DI/clot/Clotting.html 8. Behe M. (2000). In Defense of the Irreducibility of the Blood Clotting Cascade: Response to Russell Doolittle, Ken Miller and Keith Robison. http://www.arn.org/docs/behe/mb_indefenseofbloodclottingcascade.htm 9. Miller questions Behe at the Question and Answer session at the American Museum of Natural History meeting, April 23, 2002. 10. Inlay M. (2002). Evolving Immunity: A Response to Chapter 6 of Darwin's Black Box. Talkdesign.org http://www.talkdesign.org/faqs/Evolving_Immunity.html == How do the allele frequencies change over time? Common descent is a fact and allele frequency changes occur via common descent, species come from preexisting species, you had parents. There is no problem except in someones understanding of the situation. Macro changes reflect allele frequency changes. The simplest definition of evolution is change in allele frequency over time. This definition includes all possible cases of genetic evolution. If allele frequencies do not change you do not get biological evolution. It is that simple. It doesn't account for cultural evolution, but that is rarely included in biological evolution. Cultural evolution can also result in selection of different alleles. If you want to propose a definition that is less succinct and less accurate, go ahead just don't expect science to do it. == Very early in fetal development, already in the egg, one end of the embryo is designated as the front end, and the other as the rear end. Some signal substance (the substance is known, is generated by the front end, and spreads gradually along the embryo. This produces a concentration gradient, so that cells near the future hear are exposed to a high concentration of this substance, and cells near the future tail see less of it. This enables each cell to read its own position along the embryo, and enables it to decide whether to grow into a head or a tail or whatever in between. Similarly for front-to-back and left-to-right. Later on, the embryo is divided into segments, through other signalling substances that are produced in alternating "stripes" across the embryo. After that, a specialised set of genes, called Homeobox (Hox) genes, kick in. There is a sequence of such genes, called Hox1, Hox2, and so on (some critters, like humans, have several sets. In the first few segments, Hox1 is turned on, in the next Hox2, and so on. Each cell in the body now knows which segment it is in, and the different Hox genes turn on other genes, appropriate for each segment. For example, the Hox gene that is turned on in the segment where arms are supposed to grow, turns on the genes for arm growth, and so on. As for blood vessels, their growth is largely not under direct genetic control. Instead, new tissue that needs blood supply simply sends out a special signaling substance -- and blood vessels simply grow towards any source of that signalling substance. (Incidentally, cancer tumors exploit this mechanism to get a blood supply -- and some anti-cancer drugs work by blocking that signal.) It's very complicated, but not really deeply mysterious. In all cases that have been analysed in enough detail, natural mechanisms have been found. Some of it has to do with gene regulation and with cells exchanging protein signals. There are complicated regulatory networks in which proteins produced by gene A cause gene B to be switched off and gene C to be switched on, which produces a protein that causes gend D to be switched on, etc. Some of these proteins diffuse from the cells producing them into the intercellular matrix, where they influence the expression patterns of other cells. If there are several proteins diffusing from different sources, all exerting influences on overlapping sets of genes, you can get quite a complicated pattern. Some of it is mechanical, having to do with simple effects of the rate of cell proliferation and which cells adhere to which other cells. If, for example, you have a disk of cells that divide only on the top side of the disk, and remain attached to each other and to the substrate along a disk-shaped section, you will get a cylinder of cells. And this can get a lot more complicated. That's part of the genetic regulation. In most animals investigated, there is a gradient of different proteins deposited in the egg by the mother that create both front-rear and top-bottom axes before any cell division happens. This causes the earliest cells produced by the egg to already have different patterns of gene expression. As the embryo grows there are more and more local patterns of expression that do tell cells where they are. A gradient of Hox gene expression in arthropods (or chordates) determines which segment along the body axis (or central nervous system) a cell is in, and what organs will be produced there. By their extracellular environments and their history. That is, by present and past chemical (mostly protein) signals. There is also some information in direct contact with other cells or substrates. Not in great detail for most specifics, but we do know much of the general outline. A modern developmental biology text will tell you much more. So far as we can tell, it's all just chemistry and physics. == There are, currently, 8 specimens of Archaeopteryx known. Archaeopteryx has a long, bony tail. Opisthocomus has a pygostyle. Archaeopteryx has teeth. Opisthocomus does not. Archaeopteryx has three separate digits in the hand. Opisthocomus has a fused carpometacarpus and reduced, fused digits. Archaeopteryx has no keeled sternum. Opisthocomus has a keeled sternum, though the keel is smaller than in most other flying birds. I could go on and on with this, but in general, Archaeopteryx resembles other dinosaurs, while Opisthocomus resembles other modern birds. Chickens and hoatzins are, after all, both neognaths and both neorniths. === New World monkeys shared a common ancestor with us 30 million years ago. == Weren't Darwin and Huxley on the list of authors whose books were to be burned? Weren't human racial differences declared to be the result of special creation, and not evolution, in the preamble to the Nurenberg Racial Laws of 1935? == 1. Nonliving matter spontaneously produced living matter at biogenesis. 2. Spontaneous biogenesis probably only occurred once, so that all present-day life descended from one single primeval cell. 3. The different bacteria, plants, and animals are all descended from one source--they are all interrelated phylogenetically. 4. Metazoa developed spontaneously without plan out of protozoa according to the principles of chance mutation and natural selection. 5. The vertebrates are all phylogenetically interrelated. 6. The vertebrates are phylogenetically related to the invertebrates. Metazoa evolved from single-celled flagellated ancestors. === Bell, Graham. 1996. Selection: The mechanism of evolution. New York: Chapman and Hall. It's a few years out of date, of course, but it summarises and references, in some 600pp, the experimental and peer-reviewed evidence for selection without intelligent guidance. == Canola is an artificial species. Canola oil comes from the rape seed, which is part of the mustard family of plants == Cambrian phyla http://www.ucmp.berkeley.edu/phyla/metazoafr.html Of course we have to argue about what a phylum is, and whether stem-groups belong to them, or whatever. But most of the weird Burgess animals fall at least into the stem groups of extant phyla. Right now I can think only of halkieriids, Dinomischus, and Nectocaris as potential exceptions. Add that to known Cambrian/Precambrian phyla, and you come up with just 15. == Darwinism says that evolution occurs as a result of the natural laws of physics and chemistry acting on purely random mutations in organisms. The origin and development of life is explained entirely in this way. The main driver (not necessarily the only one) is natural selection. Natural selection means that only those organisms that survive and breed leave offspring, so their traits are passed on. All other drivers -- for example, constraints on development -- are equally the outcome of law and chance. **Regarding macro-evolution: We know it happens. After all, there were trilobites in the Cambrian, but not horses. There are horses today but not trilobites. == Darwin's title is _[On] The Origin of Species by Means of Natural Selection, or the preservation of favoured races in the struggle for life_ (the On was dropped from the trd edition . This title was given by the publisher Murray. Darwin's own title was _On the Origin of Species and Varieties by Means of Natural Selection_ and the subtitle was proposed by Murray to explain the novel term Natural Selection. It has literally nothing to do with the social construction of human racism, The title that *Darwin* originally gave to the book was An Abstract of an Essay on the Origins of Species and Varieties through Natural Selection s publisher encouraged a change to the title. == Serine determined chirality of life? Serine at the Start of Life Adapted from Z. Takats et al. Clusters of the amino acid serine may have lent a hand during life's origins. Many biomolecules, such as DNA, carbohydrates, and amino acids, have right- or left-handed conformations. Chemists struggle to control handedness, or chirality, in the lab, but nature generally uses only left-handed (L) amino acids and right-handed (D) sugars. Purdue University's Graham Cooks says serine may have dictated this preference. Unlike other amino acids, serine forms stable clusters exclusively from D or L forms that can interact with other amino acids. Now, he has found that serine forms stable clusters with biological molecules such as glyceraldehydes and phosphoric acid, and metals such as copper and iron, ingredients likely to have been present at the start of life. If prevalent, left-handed serine clusters would have influenced many other reactions. Once left-handed clusters had been selected for, this would have led to L-amino acids and D-sugars accumulating, says Cooks, tipping life towards its present handedness.1 Cooks' experiments could be of utmost importance in explaining how handedness was propagated, even if they do not explain its origin, says Christoph Schalley of Bonn University. Yet, while the result is very interesting, says Glasgow University's Laurence Barron, It's just one of a plethora of plausible starting points for the origin of prebiotic biomolecular handedness, any one (or none) of which might have had something to do with it. --David Bradley 1. Z. Takats et al., Serine octamer reactions: == An allele is a version of a gene. For example, the gene for eye color in humans has separate alleles for blue and brown eyes (and probably other alleles as well). The gene for hemoglobin A has many documented alleles, each of which codes for a slightly sequence of amino acids in this protein. Mutations create new alleles of the genes to which they occur (of course, the can change one allele to another than already exists in the population -- many mutations occur over and over again in a population)(and of course some mutations duplicate existing genes, producing two copies of the same allele, one or both of which may mutate in some future generation to produce a new allele). A mutation does indeed cause the frequency of some allele (the percentage of the population which carries that particular variant of that particular gene) to rise (not necessarily from zero) by some small increment. Obviously mutations are the only way any allele can increase from zero frequency. But for the most part change in allele frequencies is the result either of genetic drift (by sheer chance, some alleles are passed onto the next generation more often than others) or by natural selection (some alleles make the organism better able to find food, avoid becoming food, survive infections, find a mate, etc., and others make it more likely to die without reproducing). For example, the allele for black coloration is beneficial, and increases the individual's average number of offspring, in peppered moths resting on soot-covered branches, but is deleterious on lichen-covered branches. The frequency of the allele varies in part according to its value as camoflage. A single allele is very unlikely to create a new species, whether it occurs in one individual or an entire species. But the accumulation of many alleles can modify a population so that it no longer belongs to the same species as its ancestors, and can no longer interbreed with members of other populations whose ancestors belonged to the same species. Differences in alleles can alter the size, shape, even number of various bodily structures (rib number and even finger number are variable in humans, and the variations are inheritable), as well as behavior (otherwise humans could hardly breed dogs for different behaviors), and changes in allele frequency within a population can gradually build up major changes in morphology and behavior. Well, it is possible in principle for evolution not to happen -- for a population, at least for a time, not to undergo anything that meets the definition of evolution. And it is conceivable that evolution might be constrained from going beyond certain limits -- that changes in allele frequency might never be enough to generate a new species, or dramatic adaptions. It would appear that evolution is not in fact so limited -- but that is not a consequence of the definition. But that's not all evolution does. In fact, that's not what evolution is doing most of the time. A population evolves to deal with particular dangers in the environment (whether plants evolving resistance to heavy-metal poisoning in the vicinity of abandoned mines, or elephants without tusks becoming commoner in parts of Africa where ivory hunters are common), without becoming a new species in the process. as noted above, changes in allele frequencies can accumulate to produce a new species. Cascades are different. The individual proteins/enzymes that make up a cascade do not work together at the same time. Because of this, the function of the cascade will not be completely destroyed if one of the start proteins is removed. The rest of the cascade will still function just fine. An enzymatic cascade is even simpler since a specified order of the required enzymes is not so important. As long as all of the required enzymes are there floating around randomly, the sequential degradation of the substrate will take place just fine. You see, a specified order of the enzymes is not needed. They can be in any order here. However, if a function is dependent upon multiple proteins all working together at the same time, as in the case of bacterial motility systems like the flagellar apparatus, then the ballgame is a bit different. But, even such enzyme cascades are very difficult to evolve from scratch. If only one or two point mutations are needed to proteins that are already available to the cell, then such evolution is not a problem, even if multiple proteins are involved (as was the case with Hall's E. coli lactase evolution experiments where at least two independent mutations were required before the lactase function could be realized). However, if the genes in question are removed completely, the evolution of even a simple multi-enzyme cascade will never take place in anyone's lifetime o or even millions of years. Also, I wouldn't call the genetic engineering in this case natural evolution by random mutation and natural selection. A fair amount of intelligent design was involved in this process. As it turns out, the original wild-type bacteria did in fact have the ability to oxidize polychlorinated benzenes to at least some degree to begin with. Many chlorophenol products are known to be degraded by various microorganisms, and therefore the CYP101 mutants could form the basis of novel bioremediation systems for polychlorinated benzenes. The genes encoding the three proteins of the CYP101 system can be genetically introduced into chlorophenol-degrading micro-organisms to convert chlorinated benzenes into phenols, which are then degraded by natural pathways in the host organism. However, you will note that these three genes are not evolved in these organisms, but are placed there fully formed by intelligent design. A few subsequent mutations are used later to refine their desired function, but the fact remains that these required genes did not evolve from scratch at all. I mean, certainly if Hall's E. coli could not evolve a relatively simple lactase function from scratch without the ebg or lac genes previously in place, I don't think that a function that required three complete genes is going to just spring into existence in a single lifetime or even in billions or trillions of years. The statistics are just too much to overcome by purely mindless processes. http://intl.ejbiochem.org/cgi/content/full/268/5/1460 In this particular study the authors themselves note that the De novo evolution of genes for nitrotoluene degradation during the short period seems unlikely. Instead, it is more plausible that the pathways evolve by recruiting genes that encode degradative enzymes for other compounds to assemble a functional pathway. In other words, the genes and enzymes themselves did not evolve much at all, but were already there. Because of this, very few mutations were required to achieve this relatively simple *cascade-type* enzymatic function. In fact, three recombinant strains showed activity for all three of the required enzymes, and the cosmids carried by the strains were designated pJS314, pJS315, and pJS316. Inferences from the comparison of the structural genes of the 2,4-DNT pathway suggest that the pathway came together from three sources. The initial dioxygenase appears to have originated from a naphthalene degradation pathway like that of strain U2. A large portion of the salicylate hydroxylase oxygenase component is retained but is not functional. The MNC monooxygenase was probably derived from a pathway for degradation of chloroaromatic compounds. The presence of the vestigial (with respect to 2,4-DNT degradation) ortho-ring fission dioxygenase is consistent with its recruitment from a pathway for chloroaromatic compounds. The true ring fission enzyme for 2,4-DNT degradation has a different origin. The sequence of DntD is quite dissimilar to all other described meta-ring fission enzymes, including those from naphthalene and chloroarene degradative pathways. The distinctive sequence of the ring cleavage enzyme reflects the substrate specificity observed for the THT oxygenase. The distant relationship between homogentisate dioxygenase and DntD and the association with homologs from amino acid metabolism (dntE and dntG) indicate that the lower pathway operon arose from a gene cluster for amino acid degradation. Enzymatic activities are relatively simple to achieve. If all the needed enzymes are already being made to break down a particular molecular construct in at least some selectably beneficial way (synthetic or natural), then obviously not much change or evolution is required to be able to use this 2,3-DNT molecule for energy. Unlike bacterial motility systems, enzymatic cascades need not self-assemble themselves in any *particular* way. All that needs to happen is for all the required enzymes to be present in the intracellular environment (in any order/arrangement). This is not the case for other non-cascading functions (i.e., bacterial motility) where all the protein parts are required to be in a *particular order* all working together at the same time before the function in question will be realized. The order of protein parts is not so important in cascading enzyme functions. Only the presence of the parts is important, but not so much their order. However, even though cascading systems of enzymatic function are relatively simple because of a lack of required specified order of the individual parts, cascades are still fairly complex. Without the original enzymes being there preformed, multi-enzyme cascades will most likely not evolve even in billions of years. As in the case of 2,3-DNT utilization, if all the original enzymes are preformed, some refining mutations will no doubt contribute to a more effective interaction with and breakdown of this molecule. However, without the original genes and enzymes in place to begin with, even this relatively simple enzymatic function would most likely never have evolved - even in billions of years. The authors themselves state as much when they note that the De novo evolution of genes for nitrotoluene degradation during the short period of time seems unlikely. What I am proposing is that even with billions of years available, such evolution of even this relatively simple cascading enzymatic type function would still be unlikely if the required enzymes were not already there preformed. Another thing is that these scientists did not demonstrate the evolution of this function in real time. Certainly I am not saying that this function did not evolve in real time. It obviously did. However, these scientists were not able to reproduce the actual evolution of this function in the lab. They came to their conclusions by studying the pre-existing genes and functions in those bacteria that had already evolved this function. They made comparisons between the existing genes and other known genes in other types of bacteria. Because of this, their hypothesized pathways and series of mutational events are limited in that several gaps in knowledge are involved. One of these gaps involves the gene encoding the methylhydroxyquinone reductase for the 2,4-DNT pathway - which has not been identified. As such, this experiment is not only limited in its explanatory value over a real time demonstration, but even what it proposes to explain doesn't even come close to an explanation of a multi-protein system where each of the parts work together at the same time (i.e., where a specific internal order of the individual protein parts is important). http://jb.asm.org/cgi/content/full/184/15/4219?view=full&pmid=12107140 Inferences from the comparison of the structural genes of the 2,4-DNT pathway suggest that the pathway came together from three sources. The initial dioxygenase appears to have originated from a naphthalene degradation pathway like that of strain U2. A large portion of the salicylate hydroxylase oxygenase component is retained but is not functional. The MNC monooxygenase was probably derived from a pathway for degradation of chloroaromatic compounds. The presence of the vestigial (with respect to 2,4-DNT degradation) ortho-ring fission dioxygenase is consistent with its recruitment from a pathway for chloroaromatic compounds. The true ring fission enzyme for 2,4-DNT degradation has a different origin. The sequence of DntD is quite dissimilar to all other described meta-ring fission enzymes, including those from naphthalene and chloroarene degradative pathways. The distinctive sequence of the ring cleavage enzyme reflects the substrate specificity observed for the THT oxygenase. The distant relationship between homogentisate dioxygenase and DntD and the association with homologs from amino acid metabolism (dntE and dntG) indicate that the lower pathway operon arose from a gene cluster for amino acid degradation. Enzymatic activities are relatively simple to achieve. If all the needed enzymes are already being made to break down a particular molecular construct in at least some selectably beneficial way (synthetic or natural), then obviously not much change or evolution is required to be able to use this 2,3-DNT molecule for energy. Unlike bacterial motility systems, enzymatic cascades need not self-assemble themselves in any *particular* way. All that needs to happen is for all the required enzymes to be present in the intracellular environment (in any order/arrangement). This is not the case for other non-cascading functions (i.e., bacterial motility) where all the protein parts are required to be in a *particular order* all working together at the same time before the function in question will be realized. The order of protein parts is not so important in cascading enzyme functions. Only the presence of the parts is important, but not so much their order. However, even though cascading systems of enzymatic function are relatively simple because of a lack of required specified order of the individual parts, cascades are still fairly complex. Without the original enzymes being there preformed, multi-enzyme cascades will most likely not evolve even in billions of years. As in the case of 2,3-DNT utilization, if all the original enzymes are preformed, some refining mutations will no doubt contribute to a more effective interaction with and breakdown of this molecule. However, without the original genes and enzymes in place to begin with, even this relatively simple enzymatic function would most likely never have evolved - even in billions of years. The authors themselves state as much when they note that the De novo evolution of genes for nitrotoluene degradation during the short period of time seems unlikely. But, even such enzyme cascades are very difficult to evolve from scratch. If only one or two point mutations are needed to proteins that are already available to the cell, then such evolution is not a problem, even if multiple proteins are involved (as was the case with Hall's E. coli lactase evolution experiments where at least two independent mutations were required before the lactase function could be realized). Almost all evolutionary change involves, largely, one or two mutational events (not just point mutations, but also deletions, insertions, rearrangements, duplications) in pre-existing genes. == (see e.g. K. Kato, et al., IA plasmid encoding enzymes for nylon oligomer degradation: Nucleotide sequence analysis of pOAD2', Microbiology (Reading) 141(10):2585o2590, 1995.) == The theory of evolution would be pretty clearly falsified, I think, if the human gene for actin were more similar to the fruitfly actin gene than to the mouse actin gene, or if human were more similar to mouse than to chimp, or if whale myoglobin were more similar to salmon myoglobin than to cow myoglobin. == Evolutionist and paleontologist Barbara Stahl has commented, "The serpentine form of the body and the peculiar shape of the cheek teeth make it plain that these archaeocetes [like Basilosaurus] could not have been the ancestor of modern whales." ("Vertebrate History: Problems in Evolution", New York, NY: McGraw-Hill, 1974), p. 489. *) Extremely fragmentary skeletal remains of Ambulocetus have left scientists guessing about what kind of animal it really was. Here's a quote from evolutionary biologist Annalisa Berta: "Since the pelvic girdle is not preserved, there is no direct evidence in Ambulocetus for a connection between the hind limbs and the axial skeleton. This hinders interpretations of locomotion in this animal, since many of the muscles that support and move the hind limb originate on the pelvis. J.G.W. Thewissen, S.T. Hussain, and M. Arif, "Fossil Evidence for the Origin of Aquatic Locomotion in Archeocete Whales," "Science", 263 (5144):210-212 (January 14, 1994). Perspective by A. Berta, "What is a Whale?" same issue, p. 180-181. * == http://www.peripatus.gen.nz/Taxa/Arthropoda/Trilobita/TriSys.html == A useful mutation is likely given the relative simplicity of the nylonase function (as evolved and I think did evolve, de novo, via a frame shift mutation. However, it could also be carried on plasmids by many other types of bacteria just as easily. The nylonase function is kind of a general proteolytic enzyme with low specificity (slightly more specific than other general enzymes such as H20 - but you get the point). Many different amino acid sequence of a given length would probably have an enzymatic action on nylonase to one degree or another. Of course, this makes the ratio of what works compared with what doesn't work relatively high. With a very high ratio of functional to non-functional sequences, the neutral gaps separating each of the many functional sequences are relatively small. Such relatively small neutral gaps can be crossed fairly easily and rapidly. In real life, this is exactly what we see happening, but it is only predictable given the relative simplicity of the nylonase function. However, I do disagree with the authors of this paper when they indicate that such new functions, as the nylonase function, are not true examples of de novo evolution. Certainly this is a new function that was not needed or used before the synthesis of synthetic nylon in recent times. The ability for a genetic sequence, be it preformed a slightly modified sequence is certainly an example of a new functional ability that is not based on the loss of information or the destruction or interference with a pre-established function or interaction. Certainly this would meet anyone's definition of what evolution is supposed to be capable of doing. The same can be said for what Barry Hall did with his lactase evolution experiments in E. coli. After deleting the lacZ genes in his colonies of E. coli, a completely different gene (the ebg gene) took over the task of the lactase function with just one point mutation. What are the odds of this happening? That is the question. How likely is it that another part of an organism's genetic real estate will be identical or even close to a particular beneficial function if that function were to be completely lost? Well, it is very likely for very simple functions, such as antibiotic resistance and other types of drug resistance or functions that are based on the destruction or interference of pre-established functions/interactions (the loss of eyes in cave fish would also be included in this category). The reason for this, as you know, is that the ratio of beneficial sequences compared to non-beneficial sequences in such cases is very high. However, this evolution becomes far less likely as we move up the ladder of complexity to the level of single protein enzymes - like lactase or even the very simple nylonase function. Examples of the evolution of such functions are common, but still relatively rare compared with the lowest levels of functional complexity. With one more step up the ladder, to multi-protein functions where all the proteins are working together at the same time in a specified orientation with each other, examples of evolution in action are completely absent. You see, it is much easier to define all changes in function as real evolution. Behe and others get into trouble when they try to argue that only certain types of functional changes are actually new or irreducibly complex. What I believe is a better approach is to define all functions as irreducibly complex (which they obviously are) and all changes in function as evolutionary. What needs to be done next is to categorize functions into specific types or classes of complexity. Some functions are gained by a loss of other functions. These types of functions are really the most simple of all in that they have the lowest level of functional complexity. Other functions, such as single protein enzymes, are not based on the loss of pre-established functions, but do not require very much genetic information to code for them. This is a different type or category of function which is often still within reach of the mindless processes of Darwinian-style evolution. However, there are still other categories of function that are not apparently within statistical reach of mindless evolutionary processes. This category includes those functions that are based on multiple proteins all working together at the same time in a specified relationship to each other - such as bacterial motility systems (i.e., the flagellum). interesting. Self-assembly of organelles, multi-protein gene complexes, phage and viruses, ribosomes, and essentially everything about the cell is the norm. Some duplications *are* negatively selected against (e.g., Bar eye in Drosophila). Some duplications *are* positively selected for (e.g., DHFR duplication in the presence of methotrexate). Others are selectively neutral. But redundant complexity is a common feature of genomes, even genomes as simple as yeast (about 6000 genes, most of which can be deleted with the yeast functioning normally in rich media). That means that most genes are only *conditionally* necessary for function (and that a rich media obviates their necessity). Gene families range across both taxonomic and functional boundaries, but they do not do so haphazardly. We find genes for serine proteases serving various functions, such as blood clotting and the complement system, related to genes serving functions that have nothing to do with these; more importantly, we find that these genes nest within a phylogenetic clade with genes in creatures like sea urchins, who do not have a vertebrate clotting or complement system, but which do share other phylogenetic relationships with us that have little to do with function or habitat. Gene phylogenies are built using gene sequences, not the protein sequences they code for. More recently, both the synthetic theory and cladistics predate most if not all molecular phylogenies. That these molecular phylogenies would nest not only in the way proposed by cladistics, but also produce trees significantly congruent with those made based on anatomical characteristics was indeed a prediction. For example, that whales nested not only within mammals, but specifically ungulates, had been proposed several years before the relevant molecular sequence comparisons were done. In fact, this proposal was largely *why* the comparisons were done. That they would also nest molecularly was a prediction that could have been falsified, but was not. There are many papers available on self-assembly of various structures in a cell. The details are heavy going Clathrin self-assembly is mediated by a tandemly repeated superhelix by Joel A. Ybe, Frances M. Brodsky, Kay Hofmann, Kai Lin, Shu-hui Liu, Lin Chen, Thomas N. Earnest, Robert J. Fletterick, Peter K. Hwang in Nature 399 (27 May 1999) pp 372-375 doi:10.1038/20708 A single allele is very unlikely to create a new species, whether it occurs in one individual or an entire species. But the accumulation of many alleles can modify a population so that it no longer belongs to the same species as its ancestors, and can no longer interbreed with members of other populations whose ancestors belonged to the same species. Differences in alleles can alter the size, shape, even number of various bodily structures (rib number and even finger number are variable in humans, and the variations are inheritable), as well as behavior (otherwise humans could hardly breed dogs for different behaviors), and changes in allele frequency within a population can gradually build up major changes in morphology and behavior. == (Woese, Carl. 1998. The Universal Ancestor. Proceedings of the National Academy of Sciences USA 95:6854-6859). (Maley, Laura E. and Charles R. Marshall. 1998. The Coming of Age of Molecular Systematics. Science 279:505-506). (Patterson, Colin, and others. 1993. Congruence Between Molecular and Morphological Phylogenies. Annual Review of Ecology and Systematics 24:153-188). == There were 100 species of ape in the Miocene, argues that although the ape lineage started in Africa the great apes originated in Eurasia, with the lineages including Sivapithecus giving rise to orangutans and the lineage including Dryopithecus migrating back to Africa and giving rise to humans and the other surviving African apes. (The land bridge in the Middle East has been intermittent, depending on sea levels.) == Most animals do not have the luxury of keeping the elderly around. Among the hominids (and humans in particular) this characteristic has been exaggerated. The majority of our behavioural phenotype is transmitted after birth, rather than at conception. "Culture" is transmitted to individuals, mainly from parents (or at least parents/guardians tend to be very powerful transmitters) but also from peers, unrelated individuals, grandparents, siblings, children, etc. as well as through trial and error individual learning. Picture a community of hominids in an environment with unpredictable productivity of food resources. Generally, productivity is reasonably high, but every few decades El Nino/NAO or whatever causes dramatic changes in rainfall patterns. Having someone around who can say "well *last time* this happened, we went over the hill and stayed by the river in the next valley until the rain came back" could be really helpful. Others have already mentioned the "Grandmother hypothesis," in which elder females (who are no longer as spry and sharp eyed as they once were) care for infants so the mothers can (a) collect food (they can travel farther, faster, and see better than the elders, producing a net increase in food collected over the alternative) and (b) begin producing more offspring sooner than they otherwise could. Third, because we gain so much of our behavioural information from cultural transmission, there should be a preference for learning from elders. If an individual learns exclusively from peers, there is a non-zero chance that those peers are likely to die before reproducing. If one preferentially listens to one's grandparents, the chance of the information source dying before reproducing are zero, since if they had, you would not be there to listen to them! Thus preferentially emulating those who have survived and reproduced, as opposed to those who have not yet done so, increases one's own chance of surviving to reproductive age. == Evolution is a population altered by natural selection. Natural selection is when the members of a population are filtered by their interaction with the environment they live in. == Modern theory says, basically, only that creatures change over time. Usually, that change involves adapting to the environment or to a unique ecological niche, which usually has nothing at all to do with an increase in complexity. Case in point: Tapeworms, as parasites, are vastly *less* complex than free-living flatworms. They have evolved to be *simpler* creatures than they once were, simply because complexity isn't necessary for their survival in the protected environment of the guts of their host. == Full citation is Cutler, A. H., and K. W. Flessa. 1990. Fossils out of sequence: Computer simulations and strategies for dealing with stratigraphic disorder. Palaios 5:227-235. Disorder isn't all that common a feature, except on very small scales, of around a meter or so. And this is explainable by small scale processes such as bioturbation and short-period reworking, i.e. before lithification. Widespread out of order fossils just don't happen. On a higher level, there are many cases in which strata are out of order, but they show obvious signs of the geological processes that made them so, such as overthrusting and folding, and the correct order can generally be deduced from the structural geology, without regard to any fossils. == The first 2.5 billion years of the fossil record consist entirely of prokaryotes. The first single-celled eukaryote fossils are around 1 billion years old. The first multi-cellular fossils are very simple, and are around 600 million years old, with gradual increases in == Hume's Maxim stating that ...no testimony is sufficient to establish a miracle, unless the testimony be of such a kind, that its falsehood would be more miraculous, than the fact, which it endeavors to establish. == Jonathan Wells, a cell biologist, religious scholar, and author of Icons of Evolution, points to a few misleading photos, old drawings, and misguided experiments as evidence that Darwinism is a fraud. == Molecular Evolution, by Wen-Hsiung Li. == A scientific debate in the 1780s on the Linnean system of classification of species spilled over into the question of human racial categories. The "chain of being" of the Linnean system became a hierarchy in which it was argued that blacks fit half way in between men and apes." WINTHROP JORDAN, WHITE OVER BLACK; AMERICAN ATTITUDES TOWARD THE NEGRO 1550-1812 cf. (Loyola Journal of Public Interest Law Fall, 2001 3 Loy. J. Pub. Int. L. 1 ARTICLE: The Founders and Slavery: A Crisis of Conscience Tania Tetlow) === The fact of evolution refers to direct observations of change; the theory of evolution refers to inferences like common descent. http://www.talkorigins.org/faqs/faq-speciation.html http://www.talkorigins.org/faqs/speciation.html http://evolution.berkeley.edu/ == "Living fossils" which refer to living species whose morphology has changed very little from their ancestral forms. Now, there are also so-called "ghost taxa" (living groups with little or no fossil record -- there are quite a few of these) and "Lazarus taxa" (groups with a fossil record, but which disappear from the fossil record for millions of years -- e.g. the coelancanth). Fossilization is a rare and haphazard process. Species in some environments are fossilized fairly often (99.99+% of individuals in these environments aren't fossilized, of course), and in other environments fossilization almost never occurs. Evolutionists do not try to hide these things, but to discuss and understand them. By the way, the coelancanth was never held to be an example of a fish turning into an amphibian. It was (and still is) regarded as more closely related to the first tetrapods (land vertebrates) than other fish, but it was always regarded as a fish. == The early reptile-like mammals had a lot more teeth than modern mammals do, and in modern mammals the tooth count varies. == Christian evolutionists Theodosius Dobzhansky and Kenneth Miller. == What is the smallest known organism to contain all the chemicals needed for independent life? It's the pleuropneumonia organism, == "Transitions"book by Maynard Smith and Szathmary. They analyzed the code both from the perspective of the resultant code (top down) as well as working from the bottom up to analyze what sort of code might be expected to have evolved. The arguments are both chemical and mathematical, and apparently simulations back up the idea that the code is close to optimal in certain respects. == Evidences for Macroevolution: The Scientific Case for Common Descent" by Douglas Theobald == What insect devours its mother? The cecidomyian gall midge, a fly, can reproduce either by laying eggs or by parthenogenesis (reproduction without a male). In the latter method, the female's offspring develop within her tissues and when the time for their birth arrives, they eat the mother from inside == Protoceratops has, in the robust (probably male) form, the hint of the nasal horn that becomes so elaborated in other later Ceratopsian species. == Most change in bacteria is more likely to involve biochemical difference, such as the acquisition of a changed surface membrane than something that can be observed in a microscope. But there are mutations (single genes) that do convert E. coli from a coliform organism into one that is round rather than rod shaped and other mutations that affect its ability to form 'colonies'. And, of course, there are other mutations that are much more complex that lead to bacteria being able to utilize resources differently (even to the point of requiring what, to the original strain, was toxic). Natural selection does not recognize anything. It is simply the fact that the environment interacts with organisms in a biased fashion, favoring whatever phenotypic states (although, because evolution only works through the genotype, we tend to concentrate on that part of the phenotype that is under genetic control)optimize reproductive success. It is a fact that for many organismal features there is an optimum set point. For example, organisms can increase their ability to deal with the type of damage that U.V. produces, but usually at a cost (slower replication due to more extensive proofreading, the production of chemicals that absorb damaging UV which could be used to produce other chemicals, etc.). Because the environment only weighs the *net* effect of these changes on reproductive success , natural selection naturally tends toward the optimum set point for reproductive success, which is not the same as the optimum set point for reducing errors in DNA due to UV light. When it works, the *benefit* (always measured in the coinage of 'differential reproductive success compared to the alternative')is worth the cost. When it doesn't work, either there is insufficient benefit to outweigh the cost or there is no alternative of greater benefit (that is, it is retained by simple inertia and lack of an alternative). === Brown CJ, Todd KM, Rosenzweig RF. Multiple duplications of yeast hexose transport genes in response to selection in a glucose-limited environment. Mol Biol Evol. 1998 Aug;15(8):931-42. http://mbe.oupjournals.org/cgi/reprint/15/8/931.pdf == Evolution is to biology as the periodic table is to chemistry. ====== What insect needs humans to take care of it? The Bombyx mori, a silkworm moth, has been so cultivated by humans that it can no longer fly and needs human care to survive. Is this an example of observed speciation? == Metabolite channeling in the origin of life. Science and Medicine Library, University of Toronto, Ontario, Canada. A central question in the origin of life concerns whether primitive metabolites and catalysts interacted randomly in solution, as often envisaged, or whether they were arranged from the start in ordered metabolic complexes. The latter possibility would be consistent with the hypothesis of metabolite channeling in extant cells, which holds that intermediates in many pathways are transferred directly, without diffusion, between pathway enzymes. A model on this basis is proposed in which life originated autotrophically de novo in metabolic complexes organized on FeS2 (pyrite) mineral surfaces. Because metabolites and catalysts arose at specific sites in these complexes, they could interact specifically with neighbouring species in evolving pathways prior to the existence of protein enzymes with precise substrate binding sites. In successive stages, RNA catalysts and protein enzymes could be incorporated in these arrays. The overall process may be viewed as a molecular analogue of embryonic development, with the formation and positioning of each new component continuously transforming the whole. A corollary of the hypothesis relates to the evolution of translation and the genetic code. By virtue of channeling, biosynthetically related amino acids (e.g., aspartic acid and threonine) would have arisen close together in the complex. A second premise is that tRNAs with similar base sequences, and thus similar anticodons, were also clustered together in the complex and channeled to adjacent sites. As a result of these combined effects, tRNAs with similar anticodons would necessarily have been positioned close to, and thus more likely to have been charged with, metabolically related amino acids. This mechanism affords a new rationale for the observed codon structure of the genetic code, in which biosynthetically related amino acids possess similar codons Geology Selective adsorption of L- and D-amino acids on calcite: Implications for biochemical homochirality The emergence of biochemical homochirality was a key step in the origin of life, yet prebiotic mechanisms for chiral separation are not well constrained Here we demonstrate a geochemically plausible scenario for chiral separation of amino acids by adsorption on mineral surfaces. Crystals of the common rock-forming mineral calcite (CaCO3), when immersed in a racemic aspartic acid solution, display significant adsorption and chiral selectivity of D- and L-enantiomers on pairs of mirror-related crystal-growth surfaces. This selective adsorption is greater on crystals with terraced surface textures, which indicates that D- and L-aspartic acid concentrate along step-like linear growth features. Thus, selective adsorption of linear arrays of D- and L-amino acids on calcite, with subsequent condensation polymerization, represents a plausible geochemical mechanism for the production of homochiral polypeptides on the prebiotic Earth. --- Life's Baby Steps Summary: Billions of years ago, amino acids somehow linked together to form chainlike molecules. Now scientists have discovered what may be a key step in this process - a step that has baffled researchers for more than a half a century. Based on a Carnegie Institution of Washington press release Billions of years ago, amino acids somehow linked together to form chainlike molecules. This linkage was a vital step in the development of proteins, which are found in all living systems today. Now Robert Hazen and Timothy Filley of the Geophysical Laboratory of the Carnegie Institution of Washington, and Glenn Goodfriend of George Washington University have discovered what may be a key step in this process - a step that has baffled researchers for more than a half a century. Their work, supported by NASA's Astrobiology Institute and the Carnegie Institution, is reported in the May 1, 2001, issue of the Proceedings of the National Academy of Sciences.Chirality. Chiral compounds are ones which exist in two forms (enantiomers) which are non-superimposable mirror images of each other, and so are asymmetrical. Credit: Answers Online The molecular structure of all but one amino acid is an asymmetrical arrangement of atoms grouped around carbon. This arrangement means that there are two mirror-image forms of each amino acid; these forms are designated left-handed (L) and right-handed (D). All of the chemistry of living systems is distinguished by its selective use of these L and D, or chiral, molecules Most scientists believe the first self-replicating organisms used L-amino acids, and today all living systems have proteins with only L-amino acids. Non-biological processes do not usually distinguish between L and D variants. For a transition to occur between the chemical and biological eras, some natural process had to separate and concentrate the left- and right-handed amino acids from each other. This step, called chiral selection, is crucial to forming chain-like molecules of pure L-amino acids. Hazen and his collaborators performed a simple experiment. They immersed a fist-sized crystal of the common mineral calcite, which forms limestone and the hard parts of many sea animals, in a dilute solution of the amino acid aspartic acid and found that the left-and right-handed variants of the acid molecules adsorbed (attached) preferentially onto different faces of the calcite crystal. "Aspartic acid has a negatively charged group of atoms called the 'side group' that binds strongly to calcite, probably to the positively charged calcium atoms on calcite's surface," says Hazen. "This same binding is critical to the strength of many shells, such as clam and snail shells, which are complex composite materials of calcite and proteins."Aspartic Acid. This amino acid was used in Hazen's experiments to discover that left-and right-handed variants of the acid molecules adsorbed (attached) preferentially onto different faces of the calcite crystal. Credit: Burkhard Kirste Most minerals are centric, that is their structures are not handed. However, some minerals display pairs of crystal surfaces that have mirror relationships to each other. Calcite is one such mineral. It is common today, and was prevalent during the Archaean Era some four billion years ago, when life on earth is believed first to have emerged. This study suggests a plausible process by which the mixed D- and L-amino acids in the very dilute "primordial soup" could have been both concentrated and selected on a readily available mineral surface. "I can imagine cycles of wetting and drying in a tidal pool," says Hazen. "Each time the calcite crystals are exposed to the amino-acid-rich ocean, they adsorb D and L amino acids selectively. Each time the crystal dries out, the amino acids link up to form homochiral polymers. Eventually, one of these polymers is autocatalytic - it makes copies of itself. This idea closely parallels similar scenarios that have employed clay minerals, which don't perform the chiral selection trick." Hazen says that the organic synthesis of amino acids has proven to be fairly easy. The problem, he says, has been that the pre-biotic soup was a diverse array of both right- and left-handed molecules. This study points to a mechanism that could have selected and organized the left- and right-handed molecules. "Calcite, or some other mineral surface, seems like a good candidate for the crucial steps of selecting molecules from the complex prebiotic soup, and then organizing them into larger chain-like structures - including proteins - that are crucial to life's origin," says Hazen.Limestone is made from calcite Calcite may be a good candidate for the crucial steps of selecting molecules from the complex prebiotic soup, and then organizing them into larger chain-like structures - including proteins - that are crucial to life's origin. This study highlights how geology could have interacted with other elements of the Earth to form life. But according to Hazen, this study also suggests that life could emerge on other worlds that have carbonate rocks and liquid water. "Our study tries to link key steps in life's origin - whether here or elsewhere - with plausible prebiotic planetary conditions," says Hazen. "Surface studies of Mars and the martian meteorites, for example, provide evidence for both water and carbonates, as well as organic molecules." On Earth, proteins are only made up of L-amino acids. But on other worlds, proteins might have formed from D-amino acids. This seemingly minor difference could have led to unique and unimagined forms of life elsewhere in the Universe. "The calcite mechanism I suggest would have formed both left-handed and right-handed chains," says Hazen. "I'm suggesting - as have many other workers in the field - that the ultimate success of left over right was pure chance. On other worlds, right-handed amino acids may prevail." What Next? Hazen says this initial study opens many avenues of research. Not only are there dozens of potential minerals that could have selected and organized amino acids, but there are 20 different amino acids that occur in living systems. In addition, Hazen says there are many other factors that still have to be tested. "There's so much to do!" says Hazen. "We have to study effects of temperature, pH, salinity, and concentration on the adsorption. Then there are all the studies of polymerization on calcite surfaces -- can we simulate wetting and drying cycles to make homochiral chains of amino acids? We also have to understand this adsorption on an atomic scale. We're beginning atomic force microscopy studies to image the adsorbed molecules, and will attempt to model this adsorption process." -- Shining Light on Life's Origin Doctors urge us to wear sunscreen and try to stay out of the sun. The sun's ultraviolet (UV) rays damage our skin and are a leading cause of skin cancer. UV light has been just as shunned in theories on the origin of life. The early Earth did not have an ozone layer, so UV radiation would have been 100 times today's levels. It is generally believed that the delicate molecules of life's beginning would have deteriorated under this light intensity. Many scientists say that life's origin most likely occurred in places sheltered from UV light, such as the hydrothermal vents deep under the sea. But a new study, published in BioMed Central journal Evolutionary Biology, says rather than hinder the origin of life, UV rays helped and may even have been a necessary ingredient for life's formation. Armen Mulkidjanian, with his colleagues from Osnabruck University, Germany and the National Institutes of Health, USA, used computer models to test RNA's ability to form from sugar, phosphates, and nitrogenous bases in the presence of high levels of UV light. While the researchers acknowledge that UV can be damaging to RNA, they discovered that some parts of the molecule act as a protective shield for other parts. The nitrogenous bases absorb and disperse UV radiation, protecting the RNA's pentose-phosphate backbone. "Apparently, the backbones of DNA and RNA can be rescued by the partial "victimization" of the nitrogenous bases," the scientists write. "One can assume that these bases had been selected to perform the UV-protecting function before they became involved in the maintenance and transfer of genetic information." Since double strands provide more UV protection to the RNA backbone than single-strands, the scientists suggest that base-pairing may have originated as a trait to provide greater UV protection. Only later did these bases evolve to perform their current functions. In the computer simulation, the stability of RNA under UV radiation gave the molecules a selective advantage, allowing the number of RNA molecules to increase under natural selection. "In the UV-illuminated primordial world, the probability of a UV-breakage was more than real for any compound," the scientists write. "Those that succeeded to bind a UV-quencher got a selective advantage." RNA is thought to be one of the most important molecules in the origin of life on Earth. The discovery of ribozymes led to the "RNA world" theory, in which RNA both stored genetic information and catalyzed its own replication. This presumably led to the contemporary DNA and protein world, where DNA acts as genetic storage and proteins are needed to catalyze replication. "I believe that UV radiation has often gotten a "bad rap" in the origins community, which has led many researchers to dismiss its importance," says William Hagan, an associate scientist with the New York Center for Studies on the Origin of Life. Hagan says we should recognize ultraviolet light as not only an incinerator of the organic precursors of life, but also as a fuel for creating those same materials. UV's simultaneous destructive and creative properties seem to create a paradox, but Hagan says the solution is to identify protected environments on the early Earth where the higher-energy "bad" rays were dispersed through seawater or minerals. "I just don't think that we can ignore the tremendous power of solar energy as the most abundant fuel on the early Earth." Charles Darwin thought that life could have originated "in some warm little pond, with all sorts of ammonia and phosphoric salts, light, electricity, etc. present." Researchers have reflected upon Darwin's sunlit shallow pool ever since. John Desmond Bernal, for instance, said that life could have begun in tidal regions, where molecules faced alternating wet and dry periods. The wet period would dissolve chemicals and allow them to react with each other, while the dry periods would allow the chemicals to condense, spurring further reactions. Yet the danger of UV damage prompted other scientists to suggest that a protective water layer would be necessary. Such an environment, however, would eliminate the possibility of the condensation reactions. But if Mulkidjanian's study is correct, then the UV exposure of tidal regions would not prevent the origin of an RNA world. Hagan says that he, too, favors surface environments like the tidal lagoons for the origin of life. He thinks that while hydrothermal vents may have contributed to the concentration of organic chemicals, the sun provided a more widespread and intense energy source. "I just don't think that we can ignore the tremendous power of solar energy as the most abundant fuel on the early Earth," Says Hagan. Mulkidjanian and his colleagues suggest that their hypothesis could be tested further. A reactor system could be set up to enable nucleotides to form from simpler molecules under conditions of UV-irradiation, with aluminosilicate clays added to catalyze the nucleotide formation. If confirmed by experiment, this would provide an exciting new role for UV light in the selective formation of biopolymers. Clues to Life in the Mines of Murgul Pyrite, a form of iron sulfide (FeS2) also known as "Fool's Gold." The Mine of Murgul sounds like an ominous place in "The Lord of the Rings," a dark cavern filled with menacing orcs and trolls. But, in fact, this copper mine in Turkey may help shed light on life's origin. The mine contains pyrite, a form of iron sulfide (FeS2) also known as "Fool's Gold." This iron sulfide mineral may have acted as a template for the early chemical reactions that led to amino acids, proteins, and other building blocks of life. Pyrite has been the focus of theories regarding the origin of life since 1988, when a German patent lawyer named Gunter Wachtershauser suggested that pyrite may have acted as a catalyst for the chemistry of living cells. In Wachtershauser's scenario, chemical reactions occurred on positively charged pyrite located at hydrothermal vents. These chemical reactions eventually led to the generation of oily compounds called lipids. The lipids formed a bubble around the prebiotic system, and this bubble "cell" then drifted free of the surface on which it was generated. Although the right combination of chemicals and energy for life's origin could have been present at hydrothermal vents, skeptics say that such a hot environment would have endangered the formation of delicate proteins and RNA strands. Another possible birthplace may be at the interface between land and sea. Charles Darwin thought that life could have originated "in some warm little pond, with all sorts of ammonia and phosphoric salts, light, heat, electricity, etc. present." John Desmond Bernal expanded on this idea, suggesting that life could have begun in tidal regions, where molecules faced alternating wet and dry periods. The wet period would dissolve chemicals and allow them to react with each other, while the dry periods would allow the chemicals to condense, spurring further reactions. Although the right combination of chemicals and energy for life's origin could have been present at hydrothermal vents, skeptics say that such a hot environment would have endangered the formation of delicate proteins and RNA strands. Yet the danger of ultraviolet (UV) radiation from the sun prompted others to suggest that an ever-present layer of water would be necessary for protection Matthew Edwards of the University of Toronto thinks shallow ocean waters were more likely sites for life's origin than evaporative pools. His model for the origin of life requires ocean waters at least a few meters deep. "Wetting-drying is important in prebiotic 'soup' models, since it is hard to get dissolved charged molecules like amino acids to combine otherwise," says Edwards. "In my model, amino acids are formed in situ in a developing metabolic complex. The basic ingredients are just simple substrates like carbon dioxide or carbon monoxide." Carbon dioxide and carbon monoxide were major components of the Earth's atmosphere before the rise of oxygen-producing photosynthesis. In Edward's model, these ingredients, along with energy from the sun, induced prebiotic chemical reactions on submerged pyrite. When pyrite absorbs sunlight, a weak electrical current is generated. In the Earth's early anoxic environment, this effect would have been further enhanced. This photoelectric quality could have led to carbon and nitrogen fixation. A primitive metabolism would then have developed around these fixation sites. Edwards says this process would have been very fast, occurring in a few weeks or less. The inspiration for his model came from Helmut Tributsch and colleagues at the Hahn-Meitner Institut in Berlin, who were looking at pyrite for solar cell research. After Edwards told them about the evolutionary aspect of their work, they tested natural pyrite samples from 13 different ore sites. Not all pyrite is created equal, and the chemical properties and crystal structures of the mineral determine how well the pyrite reacts to light. Pyrite samples from the Murgul mine in Turkey showed the best evidence of photocurrent voltage, perhaps indicating the type of pyrite most likely to play a role in life's origin. Helmut Tributsch and colleagues determined that the amino acid cysteine (above) would have played a vital role in life's origin, because cysteine is able to provide the chemical energy of pyrite in a form that can be utilized by primitive organisms. Image Credit: Molecular Expressions, National High Magnetic Field Laboratory The Tributsch study also determined that the amino acid cysteine would have played a vital role in life's origin, because cysteine is able to provide the chemical energy of pyrite in a form that can be utilized by primitive organisms. Acidithiobacillus ferrooxidan, for instance, uses cysteine to dissolve pyrite in order to acquire iron and sulfur. "This chemical energy may have already been relevant during the early stage of biological evolution," they write. In addition to Acidithiobacillus, other microorganisms have evolved to extract chemical energy from pyrite. Leptospirillum ferrooxidans, for instance, induces electrochemical corrosion on pyrite to recover iron. Although these organisms do not use light-driven reactions, the use of pyrite in such primitive metabolisms may indicate a relationship that stretches far back in time. These bacteria use pyrite in a process called chemosynthesis - or the production of food from chemicals. The earliest forms of life are thought to have been chemosynthetic. But the development of photosynthesis - the production of food from sunlight - was not far behind, and even may have emerged at the same time as chemosynthesis. By receiving energy from the Sun, pyrite could have set the stage for the origin of photosynthesis. It is perhaps no coincidence that many of the enzymes in modern photosynthetic organisms are metal proteins with iron-sulfur clusters. Tracking Down Photosynthesis Purple bacteria use energy from the sun but extract electrons from substances other than water, and therefore release no oxygen. Most species are strict anaerobes and live in the sediment of ponds and lakes. A modern-day photosynthetic cell harnesses light energy by using two kinds of proteins. Photosystem I protein molecules use sunlight to convert carbon dioxide into carbon and oxygen, producing food in the form of carbohydrates Photosystem II protein molecules use light to split water into hydrogen and oxygen for plant respiration. Some early organisms used Photosystem I, while others used Photosystem II. The earliest, non-oxygen producing photosynthetic organism is thought to be purple bacteria, which relies on Photosystem I for energy. Studies suggest that modern photosynthesis developed as a result of gene transfer, where genes are swapped between different organisms. This allowed the Photosystems to come together, creating the oxygen-producing photosynthesis we are familiar with today. The Photosystem proteins developed at least 2.7 billion years ago, and possibly even earlier. A recent study by Danish researchers Minik Rosing and Robert Frei suggests oxygen-producing photosynthesis - which needs both Photosystems in order to work - already could have been in place as early as 3.7 billion years ago. Life is thought to have originated 3.8 billion years ago, soon after the Earth stopped being bombarded by the many meteorites that still cluttered the early solar system. Photosynthesis could have developed at hydrothermal vents, but it only would have been able to work at the low infrared light levels generated from the vent heat. Green sulfur bacteria living off infrared light have been found living at the vents, but it is possible that rather than originating there, these bacteria migrated downwards from the ocean surface and adapted to the infrared light conditions. It seems most likely that photosynthesis developed in a region that had regular access to the sun's light. -- Shining a Light on Life Scientists Minik Rosing and Robert Frei claim to have found the oldest evidence of photosynthesis - the most important chemical reaction on Earth - in 3.7-billion-year-old seafloor sediments in Isua, Greenland. Credit: BBC News The early Earth did not have an ozone layer, so UV radiation from the sun would have been 100 times today's levels. While the delicate molecules of life's beginning would have deteriorated under this light intensity, Edwards's model avoids this problem because his pyrite is submerged, with water acting as a protective barrier against UV. But even if the molecules on the pyrite were periodically exposed to UV, Tributsch says it still may not have been a problem. Molecules within 10 nanometers from the surface of pyrite are protected against UV radiation (10 nanometers is about five times the dimension of a typical organic molecule). When a molecule absorbs UV radiation, electrons become excited for a short time. The extra energy of the excited electrons can damage the molecule. But if the excitation happens within approximately 10 nanometers of a material like pyrite, the pyrite will absorb the extra energy and release it as heat. This diffuses the energy and averts any potential damage. Tributsch suggests that chlorophyll, the light-sensitive pigment that drives modern photosynthesis, may have originated within this 10-nanometer protected region on pyrite. The chlorophyll would have become photochemically active when pushed outside this region. By remaining in contact with the still-protected organic layer, chlorophyll could have started to provide energy to primitive cells. But could this process have happened in a tidal region? In Edwards' model, there would appear to be nothing to stop waves from washing away chemicals reacting on the submerged pyrite, and diffusing them out into the open ocean. Lord of the Rings Gandalf the Great in Moria. Credit: TheOneRing.net Yet Edwards says that the molecules were at first anchored directly to the mineral surface, and a "boundary layer" would have protected the molecules bound to the pyrite. "In any situation where a liquid or gas flows by a solid body, the speed of the flow falls off progressively the closer you get to the body," he says. The boundary layer is the space where the speed of flow drops to zero. "In the origins of life situation, the point is that even under quite wavy conditions, the boundary layer would have protected the developing biomolecules from being washed away," says Edwards. If lipids were generated, these also would have prevented the molecules from washing away. "Hydrophobic molecules would have preferentially adhered to the mineral surface rather than diffused away," says Edwards. "Think of how hard it is to clean up submerged rocks after an oil spill." Tributsch adds that when modern bacteria interact with metal sulfides, slimy organic biofilms cover the sulfide surface. He says these films, which are not easily dissolved by water, form through molecular interactions between organic molecules. Chemicals bound within these films diffuse very slowly into water, yet inorganic nutrients such as phosphate can penetrate the films. "Such an organic film may be imagined as a reaction phase, confining chemicals and supporting organic evolution on pyrite," says Tributsch. While many scientists favor hydrothermal vents as the location for life's origin, the work of Tributsch and Edwards suggests life also could have originated closer to the ocean's surface. Could the clues found in the Mines of Murgul point to a final answer? -- 1. Evolutionists do not recoil from debates over the origins of life. At the end I post just a few references on the topic. This covers just 1990 to 1999 when I did some reading on the subject. Here is a nice single reference: Maynard Smith, John, SzathmIAry. 1998. The origins of life: from the birth of life to the origins of language. Oxford: Oxford University Press. Schopf, J. William. 1999. Cradle of life: the discovery of earth's earliest fossils. Princeton, NJ: Princeton University Press. All evolutionists - some think JMS is *the* evolutionist. 2. this debate has not gone on for centuries - at best it began with Arrhenius in the 1930s, or A. I Oparin in the 1920s. Prior to that, the technical and theoretical aspects for investigating it were not around, and at best it was speculation, like genetics was speculation prior to Mendel (excepting Maupertuis). In that time enormous progress has been made. 3. Since SchrI.a6dinger's 1944 _What is Life?_ we have known that thermodynamics does not prohibit the origins of life. Quite apart from Prigogine's work, which you butcher in the next paragraph, there is a large range of work showing that thermodynamics leads to increases in complexity - you could read Eigen's work on this, if you like Eigen, Manfred, and Peter Schuster. 1979. The hypercycle, a principle of natural self-organization. Berlin; New York: Springer-Verlag. Eigen, Manfred, C. K. Biebricher, M. Gebinoga, and W. C. Gardiner. 1991. The hypercycle. Coupling of RNA and protein biosynthesis in the infection cycle of an RNA bacteriophage. Biochemistry 30 (46):11005.89a11018. Eigen, Manfred, and Ruthild Winkler. 1981. Laws of the game: how the principles of nature govern chance. New York: Knopf. Eigen, Manfred, and Ruthild Winkler-Oswatitsch. 1992. Steps towards life: A perspective on evolution. Oxford UK: Oxford University Press. or Schneider and Kay Schneider, E.D, and J.J. Kay. 1994. Life as a manifestation of the Second Law of Thermodynamics. Mathematical and Computer Modelling 19 (6-8):25-48. or the followup volume to SchrI.a6dinger's seminal work Murphy, Michael P., and Luke A. J. O'Neill. 1995. What is life?: the next fifty years: speculations on the future of biology. Cambridge; New York: Cambridge University Press. But of course you won't. Of course they are - not least being which of the many *possible* pathways is the *actual* one - we may never know this. But this is not to say we cannot allow that it happened. Sheesh. You really need to read up. I have given you a few suggestions. Baltscheffsky, H. 1997. Major anastrophes in the origin and early evolution of biological energy conversion. Journal of Theoretical Biology 187 (4):495.89a501. Barbieri, M. 1998. The organic codes. The basic mechanism of macroevolution. Riv Biol 91 (3):481-513. Conrad, M. 1997. Origin of life and the underlying physics of the universe. Biosystems 42 (2-3):177.89a190. de Graaf, R. M., J. Visscher, and A. W. Schwartz. 1995. A plausibly prebiotic synthesis of phosphonic acids. Nature 378 (6556):474.89a477. Earley Sr, Joseph E. 1998. Naturalism, Theism, and the Origin of Life. Process Studies 27 (3-4):267-279. Ertem, G., and J. P. Ferris. 1996. Synthesis of RNA oligomers on heterogeneous templates. Nature 379 (6562):238.89a240. Forterre, P. 1995. Thermoreduction, a hypothesis for the origin of prokaryotes. Comptes Rendus de l Academie des Sciences Serie Iii, Sciences de la Vie 318 (4):415.89a422. Frank, S. A. 1995. The origin of synergistic symbiosis. Journal of Theoretical Biology 176 (3):403.89a410. Huber, C. , and G. Wachtershauser. 1998. Peptides by activation of amino acids with CO on (Ni,Fe)S surfaces: implications for the origin of life. Science 281 (5377):670.89a672. Huber, C. Wachtershauser G. Department of Organic Chemistry, and Technische Universitat Munchen Lichtenbergstrasse D. Garching Germany Biochemistry. 1997. Activated acetic acid by carbon fixation on (Fe,Ni)S under primordial conditions [see comments]. Comment in: Science 1997 Apr 11;276(5310):222. Science 276 (5310):245.89a247. James, K. D., and A. D. Ellington. 1997. Surprising fidelity of template-directed chemical ligation of oligonucleotides. Chemistry and Biology 4 (8):595.89a605. Kauffman, Stuart A. 1995. At home in the universe: the search for laws of self-organization and complexity. New York: Oxford University Press. Keefe, A. D., S. L. Miller, G. McDonald, and J. Bada. 1995. Investigation of the prebiotic synthesis of amino acids and RNA bases from CO2 using FeS/H2S as a reducing agent. Proceedings of the National Academy of Sciences of the United States of America 92 (25):11904.89a11906. Kochavi, E., A. Bar-Nun, and G. Fleminger. 1997. Substrate-directed formation of small biocatalysts under prebiotic conditions. Journal of Molecular Evolution 45 (4):342.89a351. Levy, M., and S. L. Miller. 1998. The stability of the RNA bases: implications for the origin of life. Proceedings of the National Academy of Sciences of the United States of America 95 (14):7933.89a7938. Lifson, S. 1997. On the crucial stages in the origin of animate matter. Journal of Molecular Evolution 44 (1):1.89a8. Lyubarev, A. E., B. I. Kurganov, and Russian Academy of Sciences Moscow Russia Bach Institute of Biochemistry. 1997. Origin of biochemical organization. Biosystems 42 (2-3):103.89a110. Matsuno, K. 1997. Molecular semantics and the origin of life. Biosystems 42 (2-3):129.89a139. Miller, S. L., J. W. Schopf, and A. Lazcano. 1997. Oparin's Origin of Life: sixty years later. Journal of Molecular Evolution 44 (4):351.89a353. Mosqueira, F. G. 1988. On the origin of life event. Origins of Life and Evolution of the Biosphere 18 (1-2):143.89a156. Muller, A. W., and University of Edinburgh U. K. Department of Biochemistry. 1996. Hypothesis: the thermosynthesis model for the origin of life and the emergence of regulation by Ca2+. [Review] [34 refs]. Essays in Biochemistry 31:103.89a119. Norris, V., M. S. Madsen, and P. Freestone. 1996. Elements of a unifying theory of biology. Acta Biotheoretica 44 (3-4):209.89a218. Piccirilli, J. A. 1995. Origin of life. RNA seeks its maker. Nature 376 (6541):548.89a549. Ruse, M. 1997. The origin of life: philosophical perspectives. Journal of Theoretical Biology 187 (4):473.89a482. Strick, J. 1999. Darwinism and the origin of life: the role of H.C. Biol 32 (1):51-92. SzathmIAry, E. 1992. Viral sex, levels of selection, and the origin of life. Journal of Theoretical Biology 159 (1):99.89a109. SzathmIAry, E., and L. Demeter. 1987. Group selection of early replicators and the origin of life. Journal of Theoretical Biology 128 (4):463.89a486. WIUchtershIUuser, G. 1997. The origin of life and its methodological challenge. Journal of Theoretical Biology 187 (4):483.89a494. Yao, Shao, Indraneel Ghosh, Reena Zutshi, and Jean Chmielewski. 1998. Selective amplification by auto- and cross-catalysis in a replicating peptide system. Nature 396:447-450. == Out of all the really big changes seen between animal groups, the move from egg laying to placental development is a strange one to question. Anyone who has studied intro biology should know that there realy is very little to change here -- both placentals and amniotic eggs have an amnion and chorion, plus an allantois and a yolk sac. These extra-embryonic membranous structures mark the group of animals called amniota -- reptiles, birds, and mammals. There are all sorts of variations -- viviparity, oviparity, oviviviparity and mammals include egg layers like the platypus, sort-of half way types like the marsupials, and the true placentals. All you have to do is retain the egg and make the chorion a permeable site of exchange for nutrients -- it is already a site of respiratory exchange in eggs. == "When the time comes for egg laying, the wasp Sphex builds a burrow for the purpose and seeks out a cricket which she stings in such a way as to paralyze but not kill it. She drags the cricket into the burrow, lays her eggs alongside, closes the burrow, then flies away, never to return. In due course, the eggs hatch and the wasp grubs feed off the paralyzed cricket, which has not decayed, having been kept in the wasp equivalent of deep freeze. To the human mind, such an elaborately organized and seemingly purposeful routine conveys a convincing flavor of logic and thoughtfulness--until more details are examined. For example, the Wasp's routine is to bring the paralyzed cricket to the burrow, leave it on the threshold, go inside to see that all is well, emerge, and then drag the cricket in. If the cricket is moved a few inches away while the wasp is inside making her preliminary inspection, the wasp, on emerging from the burrow, will bring the cricket back to the threshold, but not inside, and will then repeat the preparatory procedure of entering the burrow to see that everything is all right. If again the cricket is removed a few inches while the wasp is inside, once again she will move the cricket up to the threshold and re-enter the burrow for a final check. The wasp never thinks of pulling the cricket straight in. On one occasion this procedure was repeated forty times, always with the same result." (Woodridge, D. (1963). _The Machinery of the Brain_) Apes are social creatures, forming packs centered around alpha males; gorillas, chimps, and humans all do this. By sheer genetic impulse, we apes are predisposed to a "worldview" centered around a hierarchy at whose apex is the Man who is not only biggest and strongest, but who is also the protector and the provider, and at whose whim all blessings in the universe flow. The so-called "religious instinct" to which you refer is nothing more than our innate masochism, our biological inability to conceive of a universe in which we are not all subservient to the Master Ape, whose blessings and beneficence are the cause of all that is. Yahweh-worship, Vishnu-worship, and Odin-worship are simply local populations' variations on the same underlying theme of apeish Alpha-male-worship, a cultural gloss on a biological constant. In the end, what you refer to as man's need to submit to a higher authority or our innate predisposition to worship in a religious manner is genetically determined. === Tiny fossil found to have the world's oldest known penis 05 December 2003 A tiny fossil of a creature that lived some 425 million years ago has entered the record books as the oldest unequivocally male animal. The organism, which resembles a cross between a shrimp and a clam, sports a large penis which has been perfectly preserved in three dimensions. David Siveter, professor of palaeontology at Leicester University, said there was no doubt the fossilised creature was a male, making it the oldest unambiguous member of its sex. Professor Siveter said the fossil was found at a site in Herefordshire where soft body parts of ancient creatures have been perfectly preserved by being buried in volcanic ash before being rapidly mineralised within rocky nodules. The animal, whose Latin name Colymbosathon ecplecticos means "swimmer with a large penis", is just 5mm (2/10ths of an inch) long and a member of a group of crustaceans known as the ostracods, crustaceans like crabs and lobsters and the most complex organisms studied within the field of micropalaeontology. Three-dimensional images of the fossil, in the journal Science, were constructed by the scientists who carefully ground away layers of the rock while photographing polished cross-sections of the fossil as they went. One of the most intriguing aspects of the study was the discovery that the basic body plan of the 425 million-year-old ostracod looks essentially the same as the body plan of present-day ostracods, Professor Siveter said. "The ground plan of the fossil strikingly resembles living groups of ostracods which shows the pace of evolutionary change has not been particularly fast," he said. The copulatory organ of the fossilised male is "large and stout" which indicates that "maybe size mattered" for the ancient ostracods. "This is a male and there must have been females around. The discovery tells us something about the biology of reproduction; it provides unequivocal evidence for sex in an animal that lived in the Silurian age," he added. In addition to the penis, the scientists were able to trace the animal's entire digestive tract from mouth to anus as well as study anatomical details such as its six pairs of gills and the limbs it used for sensing, feeding and swimming. "The whole animal is amazing, We've got something we could only dream about before." === http://www.smi.stanford.edu/projects/helix/psb01/jkim.pdf Or go right to the source: Carl R. Woese Interpreting the universal phylogenetic tree Proc. Natl. Acad. Sci. USA. 2000 July 18; 97 (15): 8392-8396 Basically, the idea now is that there was massive horizontal exchange of genetic material in the early cell stages of evolution. The "tree of life" does not have a single trunk, but rises out of a bramble bush. Even the prebiotic stages (abiogenesis) most likely were just a mass of protocells or precellular structures sharing and exchanging genetic material. Out of this mess came three different ways of using most of those shared genes to build independent cells -- Archaea, Bacteria, and eventually Eukarya. With much reduced horizontal gene tranfer, these could form more typical evolutionary trees, the three domains. As for more modern times -- there is good indication that a signiicant portion of our own genome might be derived from viral intruders, a form of horizontal transfer. == Archaeopteryx fossils are feathered. They have teeth in similar numbers to a stereotypical tetrapod. Its jaw, however, is longer than that of a stereotypical tetrapod. Since the jaw has to lengthen to turn into a stereotypical avian beak, is Archy's jaw an example of a "nascent beak"? If Tony does not think so, he should describe what extra features the jaw should have to be considered a nascent beak. Protopteryx has a jaw that is similar in shape to that of a stereotypical tetrapod. It does, however, have far fewer teeth than a stereotypical tetrapod - the Zhang and Zhou (2000) specimen has one tooth per premaxilla. It also has feathers, but these feathers appear to be more primitive than Archaeopteryx. Since the jaw has to lose teeth to turn into a stereotypical avian beak, is Protopteryx's jaw an example of a "nascent beak"? If not, why not? One can, after all, begin to see the beak coming into existence, or being born. Caudipteryx also has feathers and fewer teeth (just a few on the tip of the upper jawb0ne) and a more curved jaw than Protopteryx. Since the jaw has to lose teeth to turn into a stereotypical avian beak and to become more curved, is Caudipteryx's jaw an example of a "nascent beak"? If not, why not? One can, after all, begin to see the beak coming into existence, or being born. Confuciusornis has feathers but now no teeth at all and a more clearly curved beak than Caudipteryx. Since the jaw has to lose teeth to turn into a stereotypical avian beak and to become more curved, is Confuciusornis' jaw an example of a "nascent beak"? == One organism that might have done well on ancient Mars is desulfotomaculum, which uses sulfur as its energy source. == Quote from a scientist This may come as a shock to you, but those of us who are professional scientists see our manuscripts and grant applications turned down all the time. I have just sent off a paper to a journal after being rejected by two other journals. My last grant proposal was turned down flat. The difference between real scientists and ID-ers is that we don't whine about it in public and construct conspiracy theories. Every real scientist recognizes that publication is not an entitlement. If you don't get published you brush up your work and try again. Rather, that's what real scientists do. Kooks find it more beneficial to put about conspiracy theories. == If a sequence in the genome duplicates and then one copy mutates (and this has been observed to happen), is that an increase or reduction in information? And why? Are you using a Shannon-Weaver measure of information, or Kolmogorov-Chaitin? === Dr. John M. Allman, a neuroscientist at the California Institute of Technology, and his colleagues have delved below the level of brain structure to identify a special class of neuron - spindle cells - that are relatively enormous cells that collect information from one region of the brain and send it on to other regions. They function like air traffic controllers for emotions. They seem to lie at the heart of the human social emotion circuitry, including a moral sense. At a Society for Neuroscience meeting in New Orleans last month, Dr. Allman reported finding spindle cells in an area called the frontoinsular cortex in only two species - humans and African apes. This is a region closely connected to the insula and part of the same elaborate circuitry in which emotions are generated and experienced. An adult human had 82,855 such cells, a gorilla had 16,710, a bonobo had 2,159 and a chimp had 1,853. All had more spindle cells in the right hemisphere than in the left. This particular part of the cortex is a somewhat mysterious region, Dr. Allman said. In brain imaging studies, it lights up when people look at romantic partners; perceive unfairness, deception or uncertainty about rewards; experience embarrassment; or, if they are mothers, hear infants cry. The area is part of the orbitofrontal cortex, a part of the brain that seems to have undergone an evolutionary leap forward as recently as 100,000 years ago. It is where autobiographical memories are retrieved and choices are made for governing future behavior. It is activated with moral quandaries and economic decision making. Four years ago, Dr. Allman and his colleagues identified spindle cells in the anterior cingulate of humans, African apes and orangutans but not in any other species. The anterior cingulate is an older part of the brain that participates in autonomic functions like heart rate and blood pressure, generation of vocalizations and the production and recognition of facial expressions. In humans, the experience of any intense emotion - love, anger, lust - activates the anterior cingulate. It is active during demanding tasks and when people make errors. The harder the task, the more activation. Spindle cells probably first appeared 10 million to 15 million years ago in a common ancestor of apes, hominids and humans, Dr. Allman said. Today these rare neurons are 5 to 40 times as abundant in humans as in apes. Spindle cells may help people register the general appropriateness of transactions or events, he said. They are a teaching system that takes output from social emotion circuits - I feel good about this, I don't feel good about that - and sends it all over the cortex for further action to occur. === Check out Unravelling Piltdown, John Evangelist Walsh, c. 1996. Gould's accusation of Teilhard de Chardin as an accomplice, which if accurate pretty well clears Teilhard although he considers Gould to have made an honest mistake. (Note: I do not know if Gould read and responded to that part of the book during his lifetime.) Not surprisingly Walsh goes for Charles Dawson, the original discoverer, as the forger. He was present for practically all the discoveries, or else is the sole witness to workman X told me he'd found this discovery stories which were not checked at the time. They had a gentleman's word, why talk to a laborer. And he had a history of attention-getting forgeries and plagiarism before Piltdown ever came up. Dawson died (famous) only a few years after the first Piltdown find and therefore was not around to be questioned when the fakery was discovered. http://home.tiac.net/~cri_a/piltdown/winslow.html == "The luckiest thing that ever happened to me was that my father didn't believe in God, and so he had no hang-ups about souls. I see ourselves as products of evolution, which itself is a great mystery."-- James Watson ,American == Cavalier-Smith, T. (2001). Obcells as proto-organisms: membrane heredity, lithophosphorylation, and the origins of the genetic code, the first cells, and photosynthesis. Journal of Molecular Evolution 53(4-5): 555-595. Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_ui ds=11675615&dopt=Abstract I attempt to sketch a unified picture of the origin of living organisms in their genetic, bioenergetic, and structural aspects. Only selection at a higher level than for individual selfish genes could power the cooperative macromolecular coevolution required for evolving the genetic code. The protein synthesis machinery is too complex to have evolved before membranes. Therefore a symbiosis of membranes, replicators, and catalysts probably mediated the origin of the code and the transition from a nucleic acid world of independent molecular replicators to a nucleic acid/protein/lipid world of reproducing organisms. Membranes initially functioned as supramolecular structures to which different replicators attached and were selected as a higher-level reproductive unit: the proto-organism. I discuss the roles of stereochemistry, gene divergence, codon capture, and selection in the code's origin. I argue that proteins were primarily structural not enzymatic and that the first biological membranes consisted of amphipathic peptidyl-tRNAs and prebiotic mixed lipids. The peptidyl-tRNAs functioned as genetically-specified lipid analogues with hydrophobic tails (ancestral signal peptides) and hydrophilic polynucleotide heads. Protoribosomes arose from two cooperating RNAs: peptidyl transferase (large subunit) and mRNA-binder (small subunit). Early proteins had a second key role: coupling energy flow to the phosphorylation of gene and peptide precursors, probably by lithophosphorylation by membrane-anchored kinases scavenging geothermal polyphosphate stocks. These key evolutionary steps probably occurred on the outer surface of an 'inside out-cell' or obcell, which evolved an unambiguous hydrophobic code with four prebiotic amino acids and proline, and initiation by isoleucine anticodon CAU; early proteins and nucleozymes were all membrane-attached. To improve replication, translation, and lithophosphorylation, hydrophilic substrate-binding and catalytic domains were later added to signal peptides, yielding a ten-acid doublet code. A primitive proto-ecology of molecular scavenging, parasitism, and predation evolved among obcells. I propose a new theory for the origin of the first cell: fusion of two cup-shaped obcells, or hemicells, to make a protocell with double envelope, internal genome and ribosomes, protocytosol, and periplasm. Only then did water-soluble enzymes, amino acid biosynthesis, and intermediary metabolism evolve in a concentrated autocatalytic internal cytosolic soup, causing 12 new amino acid assignments, termination, and rapid freezing of the 22-acid code. Anticodons were recruited sequentially: GNN, CNN, INN, and *UNN. CO2 fixation, photoreduction, and lipid synthesis probably evolved in the chaperones, compartmented proteases, and peptidoglycan arose prior to the last common ancestor of life, a complex autotrophic, anaerobic green bacterium. == Saier Transport Protein Database TC#3.A.10 (2003). The H+-translocating Pyrophosphatase (H+-PPase) Family. Accessed online: June 30, 2003. Source: http://cancer.lbi.ic.unicamp.br/transport/tc/msaier/3_A_10.html Proteins of the H+-PPase family are found in the vacuolar (tonoplast) membrane of higher plants, algae, and protozoa, and in both bacteria and archaea. They are therefore ancient enzymes. The plant enzymes probably pump one H+ upon hydrolysis of pyrophosphate, thereby generating a proton motive force, postive and acidic in the tonoplast lumen. They establish a pmf of similar magnitude to that generated by the H+-translocating ATPases in the same vacuolar membrane . The bacterial and archaeal proteins may catalyze fully reversible reactions. The enzyme from R.rubrum contributes to the pmf when light intensity is insufficient to generate a pmf sufficient in magnitude to support rapid ATP synthesis. Eukaryotic members of the H+-PPase family are large proteins of about 770 amino acyl residues with fifteen putative transmembrane a-helical spanners (TMSs). The N-termini are predicted to be in the vacuolar lumen while the C-termini are thought to be in the cytoplasm. These proteins exhibit a region that shows convincing sequence similarity to the regions surrounding the DCCD-sensitive glutamate in the C-terminal regions of the c-subunits of F-type ATPases (TC #3.A.2). That last bit is important because it shows a homology connection between the 1-part PPase that interconverts proton gradients and pyrophosphate, and the F0F1-ATPase (and relatives) which interconverts proton gradients and ATP in important places like your mitochondria, which is at the absolute core of oxidative phosphorylation, which is how you convert one glucose (stored energy) into 30 ATP (the cell's energy currency). But, um, that was probably in the four-years-required class. This webpage is actually not horrible. Actually, it's pretty good: http://wunmr.wustl.edu/EduDev/LabTutorials/Cytochromes/cytochromes.html The bit we're interested in is ATP synthesis by the ATP synthetase. The point I was trying to make before is that you can ditch pretty much everything else (if you're a protoorganism) as long as you have a protein that can pump protons based on an inorganic energy source like pyrophosphate. Everything else is an elaboration on that core. == Baltscheffsky, M., Schultz, A. and Baltscheffsky, H. (1999). H+ -PPases: a tightly membrane-bound family. FEBS Lett 457(3): 527-533. Source: http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?db=m&form=6&dopt=r&uid=10 523139 The earliest known H+-PPase (proton-pumping inorganic pyrophosphatase), the integrally membrane-bound H+-PPi synthase (proton-pumping inorganic pyrophosphate synthase) from Rhodospirillum rubrum, is still the only alternative to H+-ATP synthase in biological electron transport phosphorylation. Cloning of several higher plant vacuolar H+-PPase genes has led to the recognition that the corresponding proteins form a family of extremely similar proton-pumping enzymes. The bacterial H+- PPi synthase and two algal vacuolar H+-PPases are homologous with this family, as deduced from their cloned genes. The prokaryotic and algal homologues differ more than the H+-PPases from higher plants, facilitating recognition of functionally significant entities. Primary structures of H+-PPases are reviewed and compared with H+-ATPases and soluble PPases. == Genes fit onto phylogenetic trees just as organisms do; not only that, but the shape of the trees makes evolutionary sense. The trees show that genes with relatively specialized functions have branched off from genes with more general core biological functions, such as the various opsins in our eyes tracing back to more fundamental cell membrane proteins, or various factors in the blood-clotting cascade nesting as if they had progressively branched off from some sort of trypsin, a serine protease whose function, unlike those in the clotting cascade, is not predicated on a vertebrate's high-pressure circulation system. == Alaska rabbits cannot breed with Florida rabbits. Are they the same kind? == How's that for evidence: 1. It is clear that a long time ago there weren't any dogs. 2. Obviously, dogs exist now. 3. Therefore, dogs appeared when there weren't any dogs around. 4. Consequently, first dogs were produced by non-dogs. Morey, Darcy F. The Early Evolution of the Domestic Dog. American Scientist (July/August 1994), 336-347. Olsen, Stanley J. Origins of the Domestic Dog. University of Arizona Press, 1985. Sheldon, Jennifer W. Wild Dogs: The Natural History of the Nondomestic Canidae Academic Press, 1992. Thurston, Mary Elizabeth. The Lost History of the Canine Race. Andrews and McMeel, 1996. ancestors of dogs National Geographic 1/1/2002 About 12,000 years ago hunter-gatherers in what is now Israel placed a body in a grave with its hand cradling a pup. Whether it was a dog or a wolf cant be known. Either way, the burial is among the earliest fossil evidence of the dogs domestication. Scientists know the process was under way by about 14,000 years ago but do not agree on why. Some argue that humans adopted wolf pups and that natural selection favored those less aggressive and better at begging for food. Others say dogs domesticated themselves by adapting to a new nichehuman refuse dumps. Scavenging canids that were less likely to flee from people survived in this niche, and succeeding generations became increasingly tame. According to biologist Raymond Coppinger: All that was selected for was that one traitthe ability to eat in proximity to people. At the molecular level not much changed at all: The DNA makeup of wolves and dogs is almost identical. == Spectacular finds of early Cretaceous fossil flowers during the past decade have fuelled a resurgence of research into the origin of flowering plants, the "abominable mystery" that so captivated Darwin. Now Takhtajania perrieri (Capuron) Baranova & J.-F. Leroy, the only extant Africa/ Madagascar representative of the family Winteraceae, has been rediscovered in northeastern Madagascar, 85 years after its original finding. Scientists will thus once again have a 'living fossil' to study and place in the context of both extinct and other extant primitive angiosperms. == Here is a Quote from stephen Jay Gould, that can be found in the Evolution, the basic organizing concept of all the biological sciences, has been validated to an incredibly high degree, that it may be designated as true or factual. The truth you are referring to is ABSOLUTE TRUTH, which resides only in mathematics. Evolution's conclusions must always remain tentative, but this need not stretch to the point of nihilism, and we may surely state that some facts have been ascertained with enough confidence that it may be referred to as truth in the legitemate, vernacurlar meaning of the word. ( The same way that the earths spherical shape has been verified that we need not grant the flat earth society equal, or any time at all, in the classroom) It seems to me that your picking at words. I take it you are referring to the Stanley Miller experiment, whereby he tried to produce life under ideal conditions. First of all, abiogenesis is indeed improbable, but to say it has failed is gross negligence. And to claim that abiogenesis is improbable is a transparetntly feeble arguement. Creationists see the Primeval soup and Cairn crystallization theories of abiogenesis as absurd and farfetched due to their improbability. But evolution has only equipped our brains to assess probability equivalent to our own lifetime, as opposed to any geological timescale. We, remember, are being equipped with brains capapble of calculating risk under a pencil-thin beam illuminating a tiny fraction of the mathematical range of calculatable risks. If we regard abiogenesis with the timelength of 1 aeon (1 billion years) abiogenesis becomes very probable. All this has been addressed by scientists, yet creationists continue to ignore it. For further details on the precise calculations of probability, read Dawkins book The Blind Watcmaker, more specifically the chapter entitled Origins and Miracles. Or look up the modern synthesis under esoteric mathematical equations. Now let us look at the scientific consequences if Miller's experiment HAD produced life. Such a feat would suggest that life is constantly being created in oceanic hotsprings and beds. But this would be incosistent with the fact that all life shares a same base DNA sequence, often referred to as the frozen accident. This suggests that the formation of life is rare, and when it did happen, its ability to replicate and thrive put a strain on the chemical resourses, thereby preventing any other sequences forming. This, of course, is would be contradictory to Miller's results. To put it simply, If Miller's experiment had produced life, then we should esxpect to see a wide variety of DNA languages in life, as oppsed to just one. == Molecular Biology of the Cell by Alberts, Bray, et al. at == Fungi traditionally were always considered to be related to plants and their study was the job of botany departments. To be sure, it was puzzling that their cell walls consisted of chitin, a substance supplying all the hard parts of insects but not found anywhere in plants. This was simply treated as one of the typical exceptions that are so common in biology. But molecular analysis finally showed that in much of their basic chemistry fungi are quite closely related to the Animalia." == Here are some of the intermediate fossiles of reptile-mammals: Sphenacodon (late Pennsylvanian to early Permian, about 270 million years ago), Biarmosuchia (late Permian), Procynosuchus (latest Permian), Thrinaxodon (early Triassic), Probainognathus (mid-Triassic, about 235 Mya), Diarthrognathus (early Jurassic, 209 Mya), Morganucodon (early Jurassic, about 220 Mya), Hadrocodium (early Jurassic). == February 12, 2004 Fossil Find Is World's Oldest Insect Scientists have identified the oldest known insect from its fossilized jaw remains. A report published today in the journal Nature describes the creature, which lived between 408 and 438 million years ago. The results push back the earliest appearance of winged insects by nearly 80 million years and suggest that the creatures were among the first animals to arrive on land. David A. Grimaldi of the American Museum of Natural History, who wrote the paper with Michael S. Engel of the University of Kansas, describes the find as "completely serendipitous." During the course of researching a book on insect evolution, he explains, they were initially focused on another sample stored in the vault of Londons Natural History Museum. But the slide stored next to ita sample of chert (see top image) from Rhynie, Scotland, initially studied in 1928caught their interest, and they brought it back to the U.S. for further study. "I remember sticking it under my microscope," Grimaldi says, "and Michael and I kind of looked at each other and said, Holy moly, do you see what I see? These are actual true insect mandibles [jaw parts]." Specifically, diagnostic features of the jaw's joint anatomy. Specifically, diagnostic features of the jaw's joint anatomy (see bottom image) indicate that the remains belonged to a winged insect, Rhyniognatha hirsti. The oldest known evidence of winged insectsthat is, complete fossilized bodies with fully formed wings attached--dates to around 330 million years ago. ut because there is a diversity of species capable of powered flight from this time period, insects clearly evolved wings well before that time. "This chert provides a tantalizing scrap of evidence to suggest that were missing a huge amount," Grimaldi remarks, "and theres probably this wonderful progression of insects with protowings yet to be discovered." == Today, there is also much debate about whether the evolutionary "explosion" of the Cambrian was as sudden and spontaneous as it appears. Scientists long thought that rock deposits from the Cambrian held the first and oldest fossilized animals. Now, a growing body of pre-Cambrian fossils and other scientific evidence, such as genetic analysis, increasingly suggests that the developmental changes seen abundantly in the Cambrian were already underway much earlier. == Depew and Weber's book _Darwinism Evolving_ p403: Those who take a "protein-first," and a "cell-first," approach to the origin of life tend to make greater use of self-organizationl dynamics than do molecular Darwinians like Eigen (van Holde 1980). In this spirit, Jeffrey Wicken builds on the ntion of compartmentalized chemical space by appealing to the effect of energy fluxes far from equilibrium to drive the internal organization of emerging proto-cells (Wicken 1985). In this way it is possible to produce models for life's emergence in which autocatalysis, replication, and phase separation through membrane formation arise together as a single system. Chemical selection will favour autocatalytic cycles whose reliability in producing products useful for the next round of functioning is itself enhanced by their ability to capture ans tore information in macromolecules. Wicken is not a major theorist (Eigen is) but he's one of a few pioneers of this approach. == A flagellum certainly would not self-assemble from random chemistry, but is the result of a long process of evolution. The assertion has been made that the flagellum is irreducibly complex. Recent observations reveal that this is not so. The flagellum is composed of sub-units that have their own, unrelated, purposes within the cell. http://www.idthink.net/biot/flag1/ == Reproducing organisms are observed to evolve; the processes of evolution are observed to bring about new functions; and the diversity of living organisms points the way to the various intermediaries which may have existed at different times in the long lineages of living organisms. That living organisms *do* have long histories, going back millions of years, over which major changes arise in the form of organism within a lineage, is an observation which needs to be explained by any proposed explanation. That turns out not to be the case; although of course a real storm of things makes self-organization less likely, not more likely. The point is that many of the complex parts of organisms do actually spontaneously self assemble, and DNA does NOT give an assembly instructions; despite claims to the contrary. But more to the point, the whole thing of "mixed together in a random way" is the same old strawman that recurs all the time. NO ONE thinks the organisms arise by putting together parts at at random. == Complexity, as used by everyone else in science, is a property of a model which makes it difficult (or impossible) to formulate a system's overall behaviour, even when given reasonably complete information about its atomic components and their inter-relations. The point is that there are many non-living systems that are complex, and do not degenerate into some homogeneous blob of inaction. In the discussion of abiogenesis, that means we can't know how complex molecules might interact in a big stew with so many unknown variables and interactions. A stew of complex molecules may exhibit complex behavior without any controlling design or pattern -- just like something so simple as air and water creates complex systems of clouds, tornados, jetstreams, erosion, hurricanes, rivers, geysers, deltas, oceanic currents, etc. is too complex to solve it Weather is much more complex than a Boeing 747 equations That's because in turbulent flow, the only way to calculate the future state of the system is to use a model which approximates the system. That is the very definition of complex. Take a single algebraic equation of fifth or higher order. Not so easy to solve. A bit more complex than a quadratic equation. The set is much more complex than any individual equation. Questions of existence and uniqueness of the solutions are extremely difficult (and undecidable if we restrict ourselves to Diophantine equations. Bad example, since those 50,000,000 problems are independent. It is much more complex to describe the solutions of a three- or higher dimensional dynamical system than those of a one- or two-dimensional one. Strange attractors (i.e. phenomena of arbitrarily high complexity) will in general appear. See the remarks about turbulence. It can be likened to an "irreducibly complex phenomenon" which appears in non-linear differential equations (like Navier-Stokes). This has little to do with computational limitations. == There are fossils of early carnivores that are not cats or dogs, but have features of both. http://www.sdnhm.org/fieldguide/fossils/miacids.html http://www.sdnhm.org/research/paleontology/fossildogs.html http://www.ilovecats.demon.co.uk/Evolution/miacids.htm http://www.excite.sfu.ca/projects/exwork/best/bearden/evolve.htm http://www.ucmp.berkeley.edu/mammal/monotremefr.html http://www.talkorigins.org/faqs/platypus.html http://www.lostkingdoms.com/facts/factsheet53.htm http://www.amonline.net.au/fossil_sites/lightning.htm == The common ancestor of dogs and cats was most likely a species of creodont or miacid == http://www.ucmp.berkeley.edu/mammal/monotremefr.html The time and place of monotreme origin is still largely unkown. Most fossil monotremes have been found in Australia, though a Paleocene platypus tooth (Monotrematum) has recently been recovered from Argentina (Pascual et al. 1992), suggesting they were once distributed across southern Gondwana. == All the T-even bacteriophages are dsDNA viruses (although there may be ss extensions at the ends). There are also RNA viruses and viruses that switch from RNA to DNA genomes and back (retroviruses, Hepadna viruse). Viruses are typically classified on the basis of the nature of the genome in single-stranded, and, if ss, whether the strand is the + or - strand (reads the same as a mRNA or the complement, is a unitary genome or contains multiple genome segments). Further classifications involve elements of viral structure and replicative mechanism (e.g., poxviruses, rhabdoviruses. == Microbe survives boiling water, 'breathes' iron: report A microbe that thrives in boiling water and "breathes" iron has stretched the limits of where scientists believe life could exist, according to a new report. The bacteria-like organism lives in a hellish undersea environment where water boils out from underwater vents called black smokers. There is no light, the pressure of the water would instantly crush anything living on land and the water is loaded with toxic chemicals. The discovery suggests that life could exist on planets very different from Earth. It also suggests that life did not always evolve in the ways biology teaches - in warm, soupy waters bathed in sunlight on the planet's surface. Kazem Kashefi and Derek Lovley of the University of Massachusetts tested a sample of water collected about 320 kilometres off Puget Sound and nearly 2 kilometres below the surface of the Pacific Ocean. The water was collected by a University of Washington team looking for archaea, bacteria-like organisms that live in extreme environments. The area they explored can be reached only by remotely operated submarines. Known as the Juan de Fuca Ridge, it is marked by black smokers that rise the equivalent of four stories. Life has been found around the black smokers, teetering in the balance between frigid and boiling waters and often using the sulphur in the water as fuel. For example, another microbe called Pyrolobus fumarii lives in temperatures of up to 113 Celsius. But the newly discovered microbe survived even higher temperatures and did not use either oxygen or sulphur in respiration. Instead it uses iron to burn its food for energy - the role played by oxygen on most other species on Earth. "It's a novel form of respiration," Mr Lovley said in a statement. Mr Kashefi and Mr Lovley tested their sample by steaming it in an autoclave, used to disinfect medical equipment. To their surprise, they were able to grow this organism even after bringing the water to temperatures far above the boiling point - up to 121 degrees Celsius. == Science is a rarity among human enterprises in that the standard practice is to accept the stories that stand up to sanity checks rather than the ones that make you feel cozy about your worldview. == Grasses appear at the end of the Cretaceous period. Before then, grasses hadn't evolved. == One of the major architects of the modern theory of evolution is Theodosius Dobzhansky. He was instrumental for establishing the new synthesis of evolutionary biology with genetics. He was a theoretical and experimental scientist of enormous repute and ability; and he was a Christian. Nothing in Biology Makes Sense Except in the Light of Evolution by Theodosius Dobzhansky (1900-1975) Does the evolutionary doctrine clash with religious faith? It does not. It is a blunder to mistake the Holy Scriptures for elementary textbooks of astronomy, geology, biology, and anthropology. Only if symbols are construed to mean what they are not intended to mean can there arise imaginary, insoluble conflicts. As pointed out above, the blunder leads to blasphemy; the Creator is accused of systematic deceitfulness. -- Theodosius Dobzhansky == There are several other mammals with almost as extensive fossil records as horses. These include camels, rhinos, and elephants. The reasons that other evolutionary lines are not as complete could include simple bad luck in the fossilization process, the fossils could exist but in areas where no one has collected them, the fossils could have been collected and been misidentified or ignored and so on. Remember only a tiny fraction of animals die in ways that could lead to fossilization. Also even if a particular specimen exists as a fossil the odds are that the rock bearing said fossil is buried beyond easy reach or eroded into dust before anyone sees it. == "In Darwin's Shadow: The Life and Science of Alfred Russel Wallace," Michael Shermer Journal of Theoretical Biology == Consider this a 'designer of the gaps' argument. == For God so loved the world that he gave certain bacteria flagella, meanwhile leaving humans to suffer from a host of poor design decisions. == The religious argument: Jesus redeemed the sin of Adam. To these people, the Bible, and the history it is said to represent, defines a seamless morality play of fall and redemption. One cannot have the redemption of Jesus without the sin of Adam, one cannot have Adam without the rest of Genesis, so Genesis and Creation are tied tightly to these sects of Christian faith and cannot be easily set aside the way (for example) geocentrism could. It's not merely that evolution contradicts the bible, it's that it contradicts one of the two core moments in the bible == Jonathan Marks's What It Means to be 98% Chimpanzee)2003) == Evolution doesn't ring true to a huge number of people. The misconceptions promulgated by its deniers catch a lot of people's imagination; along with the usual nonsense canards of why are there still apes, dogs don't give birth to cats, it's only a theory, the following are some of the most common: - Anything not reproduceable in a laboratory isn't science. - A proof of evolution would be a proof of atheism - Anything not directly observed is speculation. (You weren't there). Those who reject biological evolution do so, usually, not out of reason, but out of unjustified vanity. - Isaac Asimov - The idea that we aren't the special creation of god means we might just not be very important at all. == Dr. William Ausich, president of the American Paleontological Society American Paleontological Society, American Geophysical Union, National Association of Geoscience Teachers, Association of American State Geologists, Society for Vertebrate Paleontology, American Geological Institute, and the Geological Society of America. == The most complex molecules yet found in space have shown astronomers how such organic matter is created. The evidence points to a rare type of star as the origin for life's building blocks. Two hydrocarbon molecules called anthracene and pyrene occur in a nebula called the Red Rectangle, 1000 light years from Earth, according to results presented at the American Astronomical Society meeting in Atlanta, Georgia. A team led by Adolf Witt of the University of Toledo, Ohio, used telescopes in Chile and Arizona to examine ultraviolet light emitted by the nebula, and found the spectral signatures of these molecules. The two molecules contain 24 and 26 atoms respectively, making them about twice the size of the previous record holder, a molecular chain of 13 atoms. They are made of linked rings of carbon atoms, and belong to a class of molecules called polycyclic aromatic hydrocarbons (PAHs). " == Bonobo: The Forgotten Ape By Frans De Waal, Frans Lantin When it comes to chimpanzees, the small, man-like apes of Africa, there are two kinds: familiar and unfamiliar. The chimps everyone knows from movies, circuses, and zoos are "common chimpanzees" or Pan troglodytes, which are widespread from central to eastern Africa. Few people have heard of the other chimpanzee species, the pygmy chimp or Pan paniscus, also called "bonobo" (bo-NO-bo), which lives within a confined range in central African rainforests. Anthropologists study bonobos as fair approximations of the common ancestor species from which apes and humans arose. Compared to common chimps, bonobos have less massive jaws, smaller heads and ears, longer limbs, a more slender build and a preference for human-like postures, including a fair amount of bipedalism or upright walking. They have dark hands and faces, head hair parting in the middle, are more acrobatic and nimble than common chimps, and just as intelligent. Because of their remote habitat and low population, bonobos traditionally have not been captured and sent to zoos. Bonobos are the only non-human primates who have sex for purposes other than reproduction. They engage in ritualized sex to alleviate group tension; conflicts often are solved by sexual behavior among the contenders and even throughout the entire group. Female bonobos experience estrus, but will copulate with males anytime, and either gender may initiate sex. == The only random thing about this is that atoms and molecules in solution diffuse around until they find an active site on some enzyme that is designed (by the DNA program) to accept those particular atoms or molecules. There's a random element as to how long it takes a particular atom or molecule to find an active site, and which of several active sites it finds. Accordingly the rates of various enzyme-controlled reactions may vary slightly from time to time. But the overall body plan doesn't vary much because of this randomness in diffusion of atoms and molecules. The overall design of each modern organism, from overall body shape down to which particular chemical reactions occur in which tissues in which organs, is almost exactly determined by the DNA program, with only a slight bit of variation due to the randomness of diffusion. In particular, it could never happen that the enzymes of a human body would accidently build a chimpanzee body due to the randomness of diffusion. == Evolution, Thermodynamics and Information,' Jeffrey S. Wicken == The amide bond is critical in proteins - it has a tendency to want to stay planar through a pi type interaction but without the rigid locking that you would get from a C=C double bond. Also, H-bonding can't be done by purely carbon containing compounds. When you look at protein structures, there is boatloads of H-bonding, including the peptide (amide) bonds. All a consequence of water being the solvent It is extremely difficult to make anything other than Si-O once Si and O get together. Here is the difficulty with going to Si in place of carbon. When we teach freshman about the periodic table, and how they are grouped into IVA (or group 14 if you like) based on similar chemical properties, students get the ideas that the chemistry is very similar. It turns out that the first row and lower rows are quite different as far as making double and triple bonds go, as well as the tendency to make 4 bonds. The reason is that the s orbitals become more stable as you go down the periodic table, leading to more of a tendency to form two covalent bonds in Si compounds rather than four. For example, disilene, the analog of ethene, would much rather be two silylenes. H2Si: , where the colon is a lone pair of electrons in the same plane as the Si-H bonds. The Si orbitals that make the Si-H bonds are almost purely p, and the lone pair orbital is almost purely s. == We can't test any single "IC" system until we know more than we do. The ID group acknowledge that until they can come up with the pathway that was used to create things like the flagellum they have to rule out all biologically relevant pathways in order to test their assertion. They can't do this so they basically have nothing. If they had their alternate mechanism of design and knew how the flagellum was designed and implimented they could compare that with the existing data, but they aren't even close. == There are 250,000 species of flowering plants today and many thousands of extinct plants that can only be found in fossils. == C14 dates originally were coming out a couple of hundred years too early for the liking of Egyptologists, who had already worked out an established chronology for pharaonic Egypt based upon the king lists. The dating specialists revisited the question and found that there had been variation curves in the past and utilised tree rings to produce dendrochronology which, in turn, provides the basis for the calibration charts & programs used by archaeologists. Dendrochronology is used to back c. 8000 BC. The calibration charts are also based upon varve analyses. Lake sediment layers == The ability of neuroactive chemicals to reprogram central pattern generators is well known. There is also a lot known about the ability of hymenoptera to produce a wide range of neuroactive compounds. There is a lot known specifically about the ability of icheumonid wasps to produce a variety of neuroactive compounds to control their host in various ways, from killing them outright to paralyzing them to altering their behavior. == The job of the hippocampus appears to be to "encode" experiences so they can be stored as long-term memories elsewhere in the brain. "If you lose your hippocampus you only lose the ability to store new memories, == "Frogs, Flies, & Dandelions: the Making of Species" by M. Schilthuizen, Oxford U Press, 2001. This is available in paper. It is an excellent account of the species problem as well as an entertaining and very well written introduction to examples of speciation in action. It also fully describes the many battles that rage within evolutionary biology. _Darwin's Blind Spot_ by Frank Ryan. The latter book tells the story of modern day heretics like Lynn Margulis and James Lovelook, and the shocking suggestion that symbiosis has been a major driving force in life's evolution. The New York Times Book of Fossils and Evolution Maynard Smith's "Evolution" Peter Skelton's "Evolution" "What Evolution Is" "This is Biology." "One Long Argument" (Mayr) Berra's "Evolution and the Myth of Creationism. "Blueprints" by Maitland A. Edey and Donald C. Johanson == Professor David Papineau, professor of philosophy, Kings College London The evidence for evolution and natural selection is overwhelming In the distribution of current life forms the similarities and differences provide clear evidence of a common ancestor Fossils and, now, DNA, back up other types of evidence for evolution. Given the power of this evidence it would be reprehensible to teach creationism in a scientific context. However there are principles of autonomy to be considered in the matter of serious people teaching a creationism belief system without the scientific context. == The stratigraphic interval and the number of species alive today (taken as 235 for primates,are now thought to be a minimum). A painstaking review of the scientific literature revealed a total of 474 recorded fossil primate species. Applying the new approach to the data divided into stratigraphic intervals indicated that there were 8,000-9,000 extinct primate species. Broad implications These conclusions have ramifications throughout paleontology, anthropology, primatology and other disciplines. They require a rewriting of the story of primate evolution. For example, if primates originated 85 Mya, then continental drift that broke up Gondwanaland during the Cretaceous probably contributed to primate divergence. Also, the earlier date of origin indicates that primates probably originated in southern tropical/subtropical regions and then expanded northward, rather than originating in northern regions, as is currently thought. A complete lack of undoubted primate fossils from tropical and subtropical regions of the southern continents during the late Cretaceous (98-65 Mya) and Paleocene (65-55 Mya) has traditionally been taken as evidence that primates did not exist there during the Cretaceous. The first, abrupt appearance of primate fossils in the northern continents about 55 Mya is often taken as evidence for a northern continental origin during the Paleocene. Contrary to this accepted theory, the authors attribute the dearth of primate fossils during the Cretaceous and Paleocene to the fact that conditions in southern latitudes did not favor fossil preservation from those times. The earliest primates were presumably quite small, which would greatly reduce the probability of fossilization and discovery. New dates for calibrating trees Many scientists use inferred dates of origin provided by paleontologists as temporal anchors for their work. In particular, molecular biologists have relied heavily on these derived dates when constructing a timescale for evolutionary trees of animals. Molecular biologists estimate the length of time along branches between related species on these trees by estimating the number of changes in DNA sequences. However, there is no known way of deriving a timescale from molecular data alone. In order to attach a timescale to a molecular tree, the standard practice has been to calibrate it using usually only one date derived from the fossil record. If the date of origin of a group derived from the fossil record is seriously underestimated, the same must be true for any molecular tree calibrated using that date. "We hope our research will help reconcile the discrepancies between the various dates suggested by paleontologists and molecular biologists, not just for primates but for other groups of organisms, too," Dr. Martin says. Earliest common ancestor of all primates Existing primates can be divided into six subgroups: lemurs, lorises, tarsiers, New World monkeys, Old World monkeys, and apes and humans. Their 85-million-year-old earliest common ancestor probably looked like a primitive, small-brained version of today's dwarf lemur, according to Dr. Martin, who has studied primate evolution from many different perspectives for the past 30years. That animal would probably have been a nocturnal, tree-living creature weighing about 1-2 pounds, with grasping hands and feet, also used by the infant to cling to the mother's fur. It probably had large forward-facing eyes for stereovision and a shortened snout (reflecting a reduction of the anterior dentition). It would have inhabited tropical/subtropical forests, feeding on a mixed diet composed mainly of fruit and insects. Like humans, it probably had a slow pace of breeding characterized by heavy investment in a relatively small number of offspring. == Molecular Biology of the Cell - Alberts et al. (preferably 4th edition) == Achondroplasia dwarfism is characterized by abnormal body proportions. Achondroplasia in humans can be caused by a single point mutation in a number of different locations. For example, a point mutation, Gly380Arg, in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) leads to achondroplasia in humans. The achondroplasia mutation G380R uncouples ligand-mediated receptor activation from down-regulation at a site where the levels and kinetics of FGFR3 signals are crucial for chondrocyte maturation and bone formation. In other words, this mutation destroyed the ability to down-regulate the G380R receptor protein. Because of this, the receptor lost its ability to be turned off and so it stays on all the time. This leads to defective chondrocyte maturation and bone formation . . . resulting in the achondroplasia phenotype. == Society of Vertebrate Paleontology Journal of Vertebrate Paleontology == The way evolution works is this: You begin with no function, then explore the immediate vicinity until you come up with a slight, selectable improvement. You do not then continue your random walk from the beginning; you explore *from that point onward*, until you get to the next selectable improvement, then explore from there, and so on. That is the definition of an evolutionary algorithm, and it is far more efficient than a random walk for the precise reason that the points of intermediate selectable functionality allow most of the dead-end possibilities to be cut out. Your hypothetical sea of neutral mutations may well exist - but evolution has a path of stepping stones by which to cross it. one such algorithm designed an improved jet turbine that outperformed configurations selected by a human engineer and by an expert system; the algorithm took approximately two days of computation on a desktop workstation to navigate a solution space containing more than 10^387 possibilities. Again, the point is precisely that a gradually increasing fitness slope allows evolutionary algorithms to exclude a vast majority of the inviable solutions.) Of course, had the evolving population taken a slightly different branching at any of these stepping stones, the end result could have been the same function, but operating in a completely different way and reached through a completely different path - or even a completely different function, but one that performs some *other* valuable utility to the organism. I alluded to this before when I pointed out that you have no way of knowing how many different functional configurations are out there. Your argument in a nutshell is this: You are, without justification, concluding that the job an organism is doing is the only one it could do; you are then, similarly without justification, concluding that the particular configuration we see is the only one that could do that job; you then go on to calculate what the odds are of striking across it by pure chance, and when you find them to be formidable, you conclude that evolution has been falsified. This is a gross misrepresentation of the way the evolutionary process actually works, and until you get past it, you will make little progress. Mathematical models for population genetics have shown the Punctuated equilibrium" effect arising in a fitness landscape with many "peaks". Some random factors may take a population "down" a peak; selection will tend to direct further change back "Punctuated Equilibrium Is Now Old hat" by Roger Lewin in Science vol 231, pp 672-673 (14 Feb 1986) The reason that the final organisms had such a high ratio of beneficial mutations is *precisely because* they were the most successful line. They are winners and the descendants of winners. At each step, the starting organisms mutated (through crossover); the unsuccessful offspring of these changes were discarded, while the successful ones became the seeds of a new generation. == No apes have tails. That is one of the characters which distinguish apes from other primates (such as monkeys and lemurs), and the traditional classification of apes is the superfamily Hominoidea, which includes (even in the older classifications) humans, chimps, gorillas, orangs, and gibbons. == Kingdom ---Phylum -----Class -------Order ---------Family ------------Genus --------------Species == Evolution assumes 1. That there be differences between one generation and the next; 2. That the differences have an influence on the ability of individuals to survive and reproduce; 3. That the differences can accumulate over a number of generations to the point of producing new species. THIS is evolution. == E. coli bacteria contains over 1,000 known soluble enzymes, many of which can be traced in the complex chains of its life cycle. == As for mutation being unable to add something novel to an organism, here is an indisputable case: A species of Flavobacterium has gained the ability to digest nylon. This is an entirely new ability, not a modification of an already existing enzyme. It cannot digest carbohydrates IIRC. Nylon only. Nylon didn't exist before 1935. It has evolved. Here's a hyperlink that talks about it in detail. http://www.nmsr.org/nylon.htm Extracted from this site: "Purification and Characterisation of 6-Aminohexanoic-Acid-Oligomer Hydrolase of Flavobacterium sp. K172," Kinoshita, et. al., Eur. J. Biochem. 116, 547-551 (1981), FEBS 1981. Key Quote: "There are two possible reasons for an enzyme to be active on an unnatural substrate: one is that an unnatural compound could be decomposed by an enzyme if it were an analogue of that enzyme's physiological substrate, and the other is that an unnatural substrate could be decomposed by a newly evolved enzyme. The data obtained in this study show that 6-aminohexanoic-acid-oligomer hydrolase has no activity on any physiological substrates, including the linear and cyclic amides and peptides tested..." We have the pre-mutation plasmid, and the post mutation plasmid, and guess what, the only differnce is the deletion mutation in the chunk of junk DNA that results in a frame shift. How unusual. oligomers and naught else. Nylonase is NOT a protease. People who think that the beta amide linkages in nylon mean that its just a funny kind of protein (which have sterically differnt alpha amide linkages) lack basic chemistry knowledge. The chemistry of nylon is radically different to anything encountered before human syntetic chemisrty, and that the bonds have quite different orientations to the bonds normal enzymes hydrolyse. == The common ancestor of mammals and marsupials is the recently discovered Eomaia. http://news.nationalgeographic.com/news/2002/04/0423_020425_firstmammal.html == Evolution, both fact and theory, are supported by millions of pieces of evidence, from several diverse lines, including biogeography, morphological (and behavioural and developmental and metabolic) homologies, the fossil record, protein, genetic and chromosomal homologies, and exaption (and whatever has slipped my mind). == "The Origins of Order" by Stuart Kauffman. The section on hypercycles and coding has some interesting ideas on how genetic codes may have originated. "Quantum Evolution" John Joe McFadden == in Yorkshire England there's about 400m thickness of Chalk, composed almost entirely of fossils of creatures the size of a pinhead...even ignoring compaction That's an awful lot of individuals. == Mutations have been observed to occur at a measurable rate but don't occur with the same probability at all loci. There is evidence that variation occurs most frequently at loci which do not control functions critical to the life proces, and less frequently at "constrained" sites, where alterations could adversely affect important functions. Every plant and animal species is a eukaryote -- an organism possessing cells with a nucleus and organelles. "Eukaryocity" is a shared trait inherited from the last common eukaryote ancestor, which implies that *every* eukaryote should be more closely related to every other eukaryote than to any prokaryote. Evolutionary theory holds that all jawed vertebrates, whether goldfish or goldfinches, inherited the jawed condition from a single common ancestor, and thus should be equally closely related to anything that diverged from their ancestry "before" that ancestor. There are a few problems with molecular clocks. A couple are expected. The clocks are stochastic rather than metronomic; their rate is constant only on average, and actually speeds up and slows down randomly (because, of course, the "ticks" are random mutation and random drift). In addition, new mutations will often "overwrite" older mutations, or reverse them, so clocks that have been running a long time will superficially appear to have been running for less time than they actually have. Both of these are understood and necessary problems, and can be compensated for. A more annoying problem, both practically and theoretically, is that different molecular clocks seem to run at very different average rates; apparently the average rate at which neutral mutations become fixed varies according to which gene or sequence is being studied. While mutation is inevitable, major evolutionary changes are not. New genese are not guranteed to spread. In other words, we have "living fossils" (which as another poster pointed out are not animals thought to have been extinct but animals that closely resemble very old species) because some species (or some population of a speciese) just never changed much. As a rule, "living fossils" (sharks being a simple, visible example) occupy stable, simple niche's where specialization can reach a point and there are no forces which would encourage change... such as the open ocean. Living fossiles are the comfortable old shoes of organisms... there's just no reason to change. == Observation: All life forms operate on five foundation principles: 1. Genetic code 1. Reproduction. 2. Catalysts 3. Metabolism == Speciation requires reproductive isolation. Most change in bacteria is more likely to involve biochemical difference, such as the acquisition of a changed surface membrane than something that can be observed in a microscope. But there are mutations (single genes) that do convert E. coli from a coliform organism into one that is round rather than rod shaped and other mutations that affect its ability to form 'colonies'. And, of course, there are other mutations that are much more complex that lead to bacteria being able to utilize resources differently (even to the point of requiring what, to the original strain, was toxic) Natural selection does not recognize anything. It is simply the fact that the environment interacts with organisms in a biased fashion, favoring whatever phenotypic states (although, because evolution only works through the genotype, we tend to concentrate on that part of the phenotype that is under genetic control)optimize reproductive success. It is a fact that for many organismal features there is an optimum set point. For example, organisms can increase their ability to deal with the type of damage that U.V. produces, but usually at a cost (slower replication due to more extensive proofreading, the production of chemicals that absorb damaging UV which could be used to produce other chemicals, etc.). Natural selection naturally tends toward the optimum set point for reproductive success, which is not the same as the optimum set point for reducing errors in DNA due to UV light. No. When it works, the *benefit* (always measured in the coinage of 'differential reproductive success compared to the alternative')is worth the cost. When it doesn't work, either there is insufficient benefit to outweigh the cost or there is no alternative of greater benefit (that is, it is retained by simple inertia and lack of an alternative). It is a demonstrable fact that absent continued selection for an energy utilizing feature (and vision certainly qualifies; it is a large consumer of energy in those organisms that use it) or a feature that is especially sensitive to infection (fungal infection of eyes is a big problem and kills fish even in environments where eyes are useful), that that feature will tend to be selected against (if an option that reduces the costs is available) in an environment where that feature has lost its benefit but retains its costs. There are a largish number of actual direct experiments that demonstrate that *changing* the environment so as to change the relative cost-benefit ratio results in natural selection producing a new set point. For example, male guppies with big flashy tails attract more babes, but also attract more predators that like to eat male guppies with big flashy tails. Changing the environment so that it either has fewer or more predators *causes* (in a non-intelligent fashion by simply favoring the differential reproductive success of the appropriate males) the appropriate change (due to selection for particular phenotypes and these changes have a genetic basis) to reset the optimal set point for tail flashiness for that environment. In fact, this phenomenon of environments producing optimal fit between organism and local environment by natural selection is so prevelant, ubiquitous, and obvious a mechanism that works in nature, it is hard to recognize that there are a few times and places where it doesn't work: specifically, in very small populations (where random events can fix in deleterious traits) or in clonal lineages that do not undergo any significant genetic exchange (where Muller's ratchet can lead to the accumulation of deleterious traits). Given that we know that vision has costs as well as benefits (and we know what those cost factors are: high energy useage, special sensitivity to fungal and bacterial infection) and that the cost-benefit ratio clearly differs underground in a particular direction because vision is irrelevant, it is hardly wild-eyed speculation to attribute the changes in eye morphology in the genes of the population to the change in cost-benefit ratio. And specifically, the changes seen in different independent eye losses in caves seem to be largely directed toward any mechanism that reduces the risk of infection due to scrapes of the eye, by selection for those mutations that prevent the developing eye from inducing a lens or external eyeball) rather than by energy consumption (which is naturally reduced in the dark anyway). That would only be the only reasonable extrapolation from direct experiment that shows what forces cause change in morphology. Do you have an alternative explanation consistent with known mechanisms? Do you have an experiment where a morphology appeared in an environment *even though* its appearance was more costly in that environment (aside from any due to random drift in small populations)? Common descent predicts which sorts of creatures *will* be found, and which *will not*. It predicts what genetic characteristics they *will* have, and which the *will not* have, for both known and yet-to-be-discovered species. During this century, we will discover many new species of organisms, both macroscopic and microscopic, both on the land and in the seas. Common descent doesn't predict that some sorts of creatures will be found and some sorts won't -- it predicts specifically what sorts of creatures will not be found. == The ring species of Herring gulls produces two quite observably distinct species at the end. And an unbroken chain of intermediates. The hominid fossils represent an observable process and, since it is hard to precisely point to a sharp boundary between late H. erectus and early H. sapiens, a reasonably unbroken chain of small changes for at least some of the steps. == Yeast hexose transporters. They did an experiment where they put yeast into media with very little sugar. The yeast eneded up with the hexose tranporter duplicated multiple times, as well as mutant versions of the duplicated transporter. Brown CJ, Todd KM, Rosenzweig RF. Multiple duplications of yeast hexose transport genes in response to selection in a glucose-limited environment. Mol Biol Evol. 1998 Aug;15(8):931-42. http://mbe.oupjournals.org/cgi/reprint/15/8/931.pdf == The darwinian prediction is that birds (and other organisms) will do whatever maximizes their expected total lifetime reproductive output. Generally, a bird can always lay more eggs, if not this year then next year, so it's not a good investment to sacrifice your life for your offspring. If you're looking for sacrifice, consider individuals that are likely to reproduce only once in their lives, many male spiders for example. == Furthermore, whenever a creationist uses such techniques to argue against evolution, they commit the fallacy of "Argument from Authority", i.e. "Such and such famous person said it, so it must be true." Mainstream science moves forward because of evidence, not the opinions of individual scientists, no matter how well-respected they are. == Nylon eating bacteria. You must remember that nylon did not exist prior to the 1930s, so the ability to ingest nylon is a novel feature that has occured at some point in the last 70-odd years. Check out http://www.talkorigins.org/faqs/mutations.html for this and other examples. In fact, I recommend you read through www.talkorigins.org == Genetic defects45 You breed them out by selection and inbreeding. If you do not select against them recessive lethals would be expected to drift in the population and could increase to the point where they are selected against (when enough individuals of the population have the recessive lethal so that it starts showing up in a significant number of progeny). The species with the highest genetic load are the obligate outcrossers. Somehow they can tell close relatives and do not breed with them. Some type of wood rat does this and has a genetic load of 15. If you don't have some inbreeding you can't select against the recessive lethals effectively. There are highly inbred lines that do not have recessive lethals, but that doesn't mean that they haven't fixed detrimental loci. A lot of these lines have reproductive problems so even though they may have gotten rid of the really bad mutations they have to live with some not so bad ones because they were fixed by inbreeding. They have to wait for reversion to select against those or outcross. There is a parthenogentic turkey line that doesn't seem to have any recessive lethals. It can produce male poults without fertilization. The egg chromosomes just double and you get a viable poult. If there were any recessive lethals in the genome you couldn't do this. They reproduce this line by breeding the parthenogenetic toms back to females of the line to produce more females, so it is a highly inbred line. There are parthenogenetic species that are triploid and depend on it for continuation of the species. The populations consist of all females, and produce all female offspring. They induce it in fish to generate isogenic genetic lines for research purposes, but I don't know how often it occurs without induction. The induction usually isn't anything complex. I think one thing that they do is to just change the pressure suddenly for the unfertilized fish eggs. I don't know why this induces chromosome doubling and embryonic development. It is also induced by fertilization by irradiated sperm that do not contribute to the genetics of the resulting embryo. the chromosome duplication step usually occurs (at least in plants like ferns where this is quite common and leads to polyploid species) in one of the mitotic steps prior to meiosis. That is, if the diploid chromosome number is 24 (2 sets of 12), there is a mitosis in which the chromosomes duplicate but do not wind up in separate nuclei. Thus, immediately prior to meiosis, each cell has 48 chromosomes. These pair up and undergo meiosis to produce eggs that have a 'haploid' set of 24 instead of 12. Certain lizards reproduce parthenogenetically by this mechanism. Another mechanism that is common in animals is a 'fertilization' by one of the polar body nuclei formed during meiosis. Eggs, when they undergo meiosis produce one egg cell with a haploid nucleus and three polar bodies, little blebs of cell with the other three haploid products of meiosis. In some species parthenogenesis is due to one of these haploid polar body nuclei re-entering the egg cell and fusing with the haploid egg cell to produce a 'diploid' egg cell similar to that which would have happened if the haploid egg had fused with a haploid sperm. Clearly speciation can work on significantly smaller time scales than 7,000 years, though not necessarily. Even dogs haven't quite reached that great dividing line from wolves, and are still interfertile, though increasingly divergent behaviors and dwindling opportunities for interbreeding will likely provide that final bit of reproductive isolation. We do occasionally see dramatic niche shifts, that probably will lead to genetic changes. The brush tongue parrot of New Zealand shifted from being a pollen specialist to sheep predation (now that is dramatic!). Apparently they peck open the sheep and use their pollen gathering tongue to eat the liver. I believe that in California a formerly endangered hawk suddenly became fairly common when they discovered that freeways made good feeding areas. American bison and sperm whales have both gotten smaller and reduced their age to maturity in response to human hunting pressures. Bison over the last 10-15 thousand years, whales in historical times. Evolution doesn't plan ahead, and can't pick out optimal solutions to problems. Evolution works with what is at hand, and usually only provides enough to ensure basic survival, not what would be "best" for the organism. == Evolution http://content.nejm.org/cgi/content/short/346/20/1513 in humans, a single-nucleotide substitution in a gene called LRP5. This mutation decreased levels of a developmental protein called Dkk-1, resulting in increased activity of the protein Wnt, which Dkk-1 normally suppresses. This increased activity of Wnt causes a cascade of effects down the line in proteins Wnt signals, including increased activity of a protein called fibronectin, which participates in bone formation. The upshot of all this is that the people who possess this gene (it's been found in one family line so far) have extraordinarily dense and strong bones, about twice as strong as those of normal humans. The mutation was first discovered when a member of this family was involved in a serious traffic accident which he walked away from with no fractures. http://www.stopgettingsick.com/Conditions/condition_template.cfm/5636/19/1 http://info.med.yale.edu/external/pubs/ym_au02/findings.html == ttp://abcnews.go.com/sections/science/DailyNews/octopus990310.html syrtensis_, that is undergoing a fairly major evolutionary change - its suckers have largely lost the ability to suck, and are instead becoming light-emitting organs, similar to those of fireflies. The scientist researching it says it would be "like if your hand turned into a lightbulb". (Note that this change did not happen all in one shot. It's very likely been going on for some time as the result of a multi-step process of mutation - we merely happened to find out about it before it was complete.) == National Geographic. 2001/11/01 Whale evolution http://www.enchantedlearning.com/subjects/whales/allabout/Evol.shtml ** http://www.talkorigins.org/features/whales/ Fish developing legs took millions of years also Acanthostega (fish with legs) http://tolweb.org/tree?group=Acanthostega&contgroup=Terrestrial_Vertebrates R. Bakker, The Dinosaur Heresies: A Revolutionary View of Dinosaurs, U.K. edition, Longman Group, Essex, 1986; published in USA as The Dinosaur Heresies: New Theories Unlocking the Mystery of the Dinosaurs and their Extinction, Morrow, New York, 1986. 2. E.J.Slijper, Whales, translated from Dutch by A.J. Pomerans, Cornell University Press, New York, (U.K. edition Hutchinson, taken over by Routledge, London, UK), 2nd edition, 1979. 3. Anthony R. Martin, Whales and Dolphins, Bedford Editions, London, p. 12, 1990. Return to text. == Here's an example of what Homo sapiens skulls looked like 160k years ago. Modern Human having apelike characteristics. Nature http://www.nature.com/nsu/030609/030609-8.html == http://www.talkorigins.org/ http://www.talkorigins.org/origins/faqs.html http://www.talkorigins.org/origins/outline.html http://www.talkorigins.org/origins/faqs-qa.html http://www.talkorigins.org/origins/faqs-mustread.html http://www.talkorigins.org/faqs/faq-misconceptions.html http://www.talkorigins.org/origins/faqs-evolution.html http://www.talkorigins.org/faqs/faq-intro-to-biology.html http://www.talkorigins.org/origins/other-links-gensci.html http://www.talkorigins.org/origins/other-links.html#evolution http://www.talkorigins.org/faqs/faq-speciation.html http://www.talkorigins.org/faqs/speciation.html http://www.talkorigins.org/faqs/evolution-research.html http://www.talkorigins.org/faqs/macroevolution.html http://www.nhm.ac.uk/hosted_sites/paleonet/paleo21/mevolution.html http://www.talkorigins.org/faqs/comdesc/ == Helycyton gartleri. It is a unicellular species of human (yes, I meant to write that) evolved from a carcinoma to survive in the habitat of laboratory cell cultures. == "Disorder" and "Entropy" ARE NOT THE SAME THING! Entropy is "unusable energy". This is not the same as "disorder". One system that becomes more orderly as entropy increases is crytstal formation. A substance cools, entropy increases, and viola, a crytsal forms which is orderly. == Mammal-like relatives) split from the Diapsids (which include lizards, reptiles, and birds, and their extinct relatives) more than 300 million years ago. At the time, there were no birds yet. So the line that eventually led to birds and the lineage that eventually produced us split from each other *long* before there were either birds or mammals. The "bird" and "mammal" designations are not appropriate until much later (around 240-260 MYA for "mammals", loosely defined, and only about 150 MYA for "birds". Our most recent ancestors were mammals. Their predecessors were mammal-like reptiles, their predacessors were terrestrial vertebrates that, were they alive today, we would probably intuitively group with the reptiles (although they were no more closely related to today's reptiles than to us). Their ancestors were acquatic tetrapods, and their ancestors would, if they were alive today, probably be intuitively grouped with the bony fish (again with the caveat that they are no more/less closely related to one set of their descendants than to the others). Their ancestors were Gnathostomata, (vertebrates with jaws,) and their ancestors were chhordates without backbones or skulls, and their ancestors were bilaterally symetrical invertebrates, and their ancestors were single-celled organisms with a nucleus, and their ancestors were similar to bacteria. I'm not sure what was ancestral to the bacteria, but a 3.6 Billion year old family tree is at least a start. == Unless you have something more to show than your feeling that the big bang and evolution can't work against the conviction of the leading men in the field that the evidence says that it did, your opinion does not have a great deal of value. It may indeed be proven wrong in the future but not by someone's feelings. == The differences between the chimp's genetic code and ours should reveal what makes us human, scientists hope. The disparities might, for example, lie in genes that control the development of the brain and language, or of human-specific diseases such as Alzheimer's, AIDS and malaria. The consortium of scientists has already lined up the chimp sequence, which is around 90% complete, with the human genome and placed it in public databases for other researchers to use. The chimp sequence is thought to be almost 99% identical to ours in some regions at least, and its full code is roughly the same size as ours: 3 billion base pairs. == Images provide dramatic evidence of the intermediate forms: http://www.talkorigins.org/faqs/comdesc/hominids.html == The Great Pummeling New geological findings support a theory that life on earth was nearly destroyed by a meteoroid 185 million years before dinosaurs died out Deep in the layers of the Earth, ancient rock shows signs of a planet, 250 million years ago, teeming with plants, fish, reptiles and proto-mammals . Then, evidence of life around the globe all but vanishes. == The Archaean occurs between the Hadean and the Proterozoic. http://www.ucmp.berkeley.edu/bacteria/bacteriafr.html http://www.ucmp.berkeley.edu/precambrian/archaean.html http://jove.geol.niu.edu/faculty/stoddard/keels.html plate bundaries == Average Life Expectancy 1850 - 38.3 years 2000 - 74.8 years == They are date-ordered by the geologists (and it turns out, by nuclear physicists). Once fish appear, they are always there. Once reptiles appear, there are always reptiles. Let's remake the list to reflect what we really see: chordates (simple) chordates, fish chordates, fish, reptiles chordates, fish, reptiles, mammals It appears that life is diversifying over time. A close look at the evidence will indicate that bones appear with fish and are adapted by reptiles and mammals; legs appear with reptiles, and are adapted by mammals. Let's make a prediction from this hierarchy. There existed an intermediate species between fish and reptiles." Guess what? We don't even have to use a shovel. They still exist today and they're call amphibians. If we look at the fossil record, they first appear after fish and before reptiles -- just as we would expect. Now our table looks like this: chordates (simple) chordates, fish chordates, fish, amphibians chordates, fish, amphibians, reptiles chordates, fish, amphibians, reptiles, mammals We can continue to fill in our tables, but it is pretty obvious what is happening. We never find reptile fossils in the strata below the first fish fossil. Never. We never find mammal fossils appearing in the fossil record before the first reptile fossil. Never. We do find, as we accumulate more and more data, intermediate species with increasing detail, and always we have the nested hierarchy. Now, consider the case of humans. We are *obviously* mammals. Taking a look at the existing fauna, it's pretty obvious we are related to (non-human) apes. Let's make a prediction from theory. "There existed an intermediate species between apes and humans." Lo and behold, we find Australopithecus, and of course, it always found in strata that is above the first appearance of apes. == While we know that evolution affects populations, not individuals, it does still start with a first occurrence, one isolated population, usually a very small one may vary from its kin in some way that enables it to vary even further, leading to a larger population of a different genus, and perhaps many more genera will arise from their descendants, but they will all start out in relatively small groups. Out of all the various and unusual species of monkeys that ever existed or still exist, only one initially small group of them ever became something noticeably more, something different from all the rest, an ape, and not "just" a monkey anymore. And the same applies to every other recent taxon as well. == It is known, and has been known for a long time, that primates do not synthesize vitamin C. And that guinea pigs don't either. The vitamin C genes of both humans and chimps have the SAME mutation that causes it not to function, while in guinea pigs, it is some OTHER mutation that causes the failure. == In the (8th? and) later editions of the Systema Naturae Linnaeus allowed for hybrids between species within a genus, but not classes. I have Stafleu's _Linnaeus: Linnaeus was a special creationist - that is, he believed that each "There are as many species as the Infinite Being produced diverse forms in the beginning."(Species tot sunt diversae quot diversas formas ab initio creavit infinitum Ens, Fundamenta botanica No. 157, 1736). However, in 1744 he was forced to allow that some species are the result of hybridisation, at least in plants, because he observed it happening. A species of plant he placed in a genus Peloria (from the Greek pelor, meaning monstrosity) was in stem and leaf structure part of the Linaria genus, but the flower was clearly different (Hagberg 1952 p196f; Glass 1959b). Still, he thought that genera were real and the possibilities for change limited. According to Larson (1967), Linnaeus imagined in the Fundamenta fructifications "that God created one species for each natural order of plants differing in habit and fructification from all others. These species, mutually fertile, gave birth to as many genera as there were different parents, their fructification somewhat changed(p317). In the Pralectiones (1744), Linnaeus went further: The principle being accepted that all species of one genus have arisen from one mother through different fathers, it must be assumed: 1) That in the beginning the Creator created each natural order only with one plant with reproductive power. 2) That by their various mixings different plants have arisen which belong to the mother's natural order as they are similar to the mother with regard to their fructifications, and are, as it were, species of the order, i.e., genera. 3) We may assume that plants have arisen within the orders, i.e. by genera of one order, may mix with each other. In this way there will arise species that should be referred to the mother's genus as her daughters. [quoted in Larson, loc. cit.] Now the "natural orders" here are not his rank of Ordo, and he clearly states that hybrids occur only within genera (which are defined by their fructification). == Evolutionary biology is not one theory, but many somewhat related theories. The key with biological life is the fractional advantage. Even a 1% increase in survival will eventually result in the entire population containing that particular gene. Even a 1% survival advantage will eventually cause the organism posessing said advantage (if the population survives long enough to reach critical mass) to fill up all available space, given sufficient time. == Many organisms possess vestigial structures that have no apparent function, but that resemble structures their presumed ancestors had. Humans, for example, possess a complete set of muscles for wiggling their ears, just as a coyote does (table 22.1). Boa constrictors have hip bones and rudimentary hind legs. Manatees (a type of aquatic mammal often referred to as "sea cows") have fingernails on their fins (which evolved from legs). Figure 22.17 illustrates the skeleton of a baleen whale, which contains pelvic bones, as other mammal skeletons do, even though such bones serve no known function in the whale. The human vermiform appendix is apparently vestigial; it represents the degenerate terminal part of the cecum, the blind pouch or sac in which the large intestine begins. In other mammals such as mice, the cecum is the largest part of the large intestine and functions in storageusually of bulk cellulose in herbivores. Although some suggestions have been made, it is difficult to assign any current function to the vermiform appendix. In many respects, it is a dangerous organ: quite often it becomes infected, leading to an inflammation called appendicitis; without surgical removal, the appendix may burst, allowing the contents of the gut to come in contact with the lining of the body cavity, a potentially fatal event. http://www.txtwriter.com/Backgrounders/Evolution/EVpage12.html == Species are the taxa from which tree diagrams are constructed. On both the Ashlockian-Mayrian notion of monophylyand the cladistic notion of monophyly, species do not form clades on their own - to form a clade one needs at least three such taxa or above (two to include and one as an outgroup). So monophyly is not a property of species (or LITUs if you like Pleijel's term) but of the trees formed from species [even crown group cladograms are implicitly single species trees, since a crown group evolved from a single species per definitio]. If you have a reticulate event (hybridisation, HGT, etc), then you have an unresolved tree, and the nodes and subsequent terminal nodes from that event are themselves neither monophyletic nor polyphyetic. The *lineages* form phyletic groups, not the species by themselves. In the case of a multiply arising species - what I am calling the Respeciation Problem in the thesis - you still do not have a polyphyletic group, because (at the phyletic lineage level) a species is not a group - it's an individual. Of course, you can have trait trees and gene trees *within* spec ies, and *these* can be monophyletic etc. == One example of a beneficial mutation comes from the mosquito _Culex_ _pipiens_. In this organism, a gene that was involved with breaking down organophosphates - common insecticide ingredients - became duplicated. Progeny of the organism with this mutation quickly swept across the worldwide mosquito population. There are numerous examples of insects developing resistance to chemicals, especially DDT - which was once heavily used in this country. And, most importantly, even though 'good' mutations happen much less frequently than "bad" ones, organisms with "good" mutations thrive while organisms with "bad" ones die out. -- http://www.fmnh.helsinki.fi/users/haaramo/Metazoa/Deuterostoma/Chordata/Syna" http://www.palaeos.com/Vertebrates/Units/460Insectivora/460.700.html All mammals essentially had one common ancestor if you go back in distant time. It was possibly a shrew-like creature", and bore a particular genetic similarity to aardvarks which "appears to be the closest match to this ancient relative in terms of how little its DNA has changed over time. Many scientists think both are members of the group from which all placental mammals evolved. That implies both primitive and closeness of relationship. The Finnish site shows several genera in Lipotyphyla that aren't shrews, but would have been ancestral to modern shrews. Soricomorpha is the same way in that there are very shrew-like critters listed in that group but actual shrews don't come along until the formation of Soricoidea. So modern hedgehogs, moles and shrews are descended from, (and thus closely-related to) Leptictidium, which are also part of Lipotyphyla and are very shrew-like but aren't quite shrews. Not necessarily. These divisions are not simultaneous by any defintion. In this case, Lipotyphla arose within Leptictidae which was already here. The first species listed in the Lipotyphla sub-group, Erinaceomorpha is called Adunator, and is identified as a lepticitid. So while the main group of Leptictidae diversified within their own group, one small lineage among them beget a whole new line distinct from the others. Some of them diversified into shrews and moles and such, but others went on to become cattle and carnivores and all that eventually. Everything from elephants and apes, whales and wildebeest all came from a series of cousins that all looked like some kind of five-toed long-bodied scale-tailed weasel-rats, which of course diversified a bit from the same shrew-like raccoon wannabe weasel-rat earlier on. == Journal of Archaeological Science Volume 31, Issue 1,(January 2004) Confirmation of a near 400 ka age for the Yabrudian industry at Tabun Cave, Israel, Pages 15-20 W. J. Rink, H. P. Schwarcz, A. Ronen and A. Tsatskin == Scientists have produced a draft map of 20,405 interactions between 7,048 proteins in the fruit fly. == Transitional fossils from early eutherian mammals to rodents: Paramyids, e.g. _Paramys_ -- early "primitive" rodent _Paleocastor_ -- transitional from paramyids to beavers _Paramys_ and its relatives gave rise to 5 enormous and very diverse groups of rodents, with many fossils. Animals classified within the order Lipotyphla have been considered to be among the most primitive living eutherian mammals. http://www.lub.lu.se/cgi-bin/show_diss.pl?db=global&fname=sci_279.html == Here are details of the five worst mass extinctions in Earths history and their possible causes, according to paleobiologist Doug Erwin of the Smithsonian Institutions National Museum of Natural History. Erwin said estimates of extinction rates are from the late John J. Sepkoski at the University of Chicago: Cretaceous-Tertiary extinction, about 65 million years ago, probably caused or aggravated by impact of several-mile-wide asteroid that created the Chicxulub crater now hidden on the Yucatan Peninsula and beneath the Gulf of Mexico. Some argue for other causes, including gradual climate change or flood-like volcanic eruptions of basalt lava from Indias Deccan Traps. The extinction killed 16 percent of marine families, 47 percent of marine genera (the classification above species) and 18 percent of land vertebrate families, including the dinosaurs. End Triassic extinction, roughly 199 million to 214 million years ago, most likely caused by massive floods of lava erupting from the central Atlantic magmatic province -- an event that triggered the opening of the Atlantic Ocean. The volcanism may have led to deadly global warming. Rocks from the eruptions now are found in the eastern United States, eastern Brazil, North Africa and Spain. The death toll: 22 percent of marine families, 52 percent of marine genera. Vertebrate deaths are unclear. Permian-Triassic extinction, about 251 million years ago. Many scientists suspect a comet or asteroid impact, although direct evidence has not been found. Others believe the cause was flood volcanism from the Siberian Traps and related loss of oxygen in the seas. Still others believe the impact triggered the volcanism and also may have done so during the Cretaceous-Tertiary extinction. The Permian-Triassic catastrophe was Earths worst mass extinction, killing 95 percent of all species, 53 percent of marine families, 84 percent of marine genera and an estimated 70 percent of landspecies such as plants, insects and vertebrate animals. Late Devonian extinction, about 364 million years ago, cause unknown. It killed 22 percent of marine families and 57 percent of marine genera. Little is known about land organisms at the time. Ordovician-Silurian extinction, about 439 million years ago, caused by a drop in sea levels as glaciers formed, then by rising sea levels as glaciers melted. The toll: 25 percent of marine families and 60 percent of marine genera. Recent analysis of South African rocks reveals that rivers suddenly became clogged with sediments 251 million years ago, indicating Earths worst mass extinction wiped out many trees and other plants that held soil in place. A huge comet or asteroid walloped Earth to cause the mass die-off at the end of the Permian Period and dawn of the Triassic although his study does not say so. Another scientist estimates the object was 9 to 12 miles (15 to 20 kilometers) wide. Previous research showed the extinction wiped out nearly 90 percent of sea species and 70 percent of vertebrate animal species on land. That made it far worse than the Cretaceous-Tertiary extinction of the dinosaurs and many other creatures 65 million years ago an event often blamed on the impact of a perhaps 6-mile- (10-kilometer-) wide asteroid. The Permian-Triassic catastrophe also stripped Earth of many rooted plants, triggering severe erosion. As a result, sedimentary rocks from that time show that large meandering rivers throughout South Africas Karoo Basin took on a braided, multichannel appearance, resembling streams in areas devastated by Mount St. Helens big eruption or areas logged by clear-cutting. Many researchers argue a comet or asteroid impact caused Earth's worst mass extinction 251 million years ago. "When you remove all vegetation, thats what clear-cutting is. The Permian-Triassic extinction was the mother of all clear-cutters. Other recent studies have found similar abrupt changes from meandering to braided river deposits during Permian-Triassic time in Australia, Antarctica and Northern Europe. That supports the notion of a global die-off of land plants, including extinction of Glossopteris trees and bushes, which resembled modern ginkos. Ward said a variety of ferns, seed ferns and early pine trees also went extinct. Until land plants evolved roughly 415 million years ago, Earths rivers were typically braided rather than meandering, he said. Braided rivers are common in Alaska and mountainous areas where glaciers and streams erode rock quickly, filling streams with sediments. The Permian-Triassic switch from meandering to braided streams once was thought due to mountain-building uplift and subsequent erosion. But mountain-building episodes in the Karoo Basin do not coincide with the Permian-Triassic extinction. The rocks indicate the rivers changed from meandering to braided within 50,000 years, then returned to normal meandering courses in another 50,000 to 100,000 years. The new study is the latest in a series showing the Permian-Triassic catastrophe was quick at least in geological terms and extremely nasty. But it has not settled debate among those who advocate various theories of what caused the extinction: an object whacking Earth, floods of lava from the Siberian Traps, climate change, and/or deadly radiation from a nearby supernova or other cosmic explosion. Marine rocks from China revealed the Permian-Triassic extinction happened in less than 160,000 years. A study of seafloor rocks now in the Austrian Alps concluded the extinction happened in less than 60,000 years and perhaps in less than 8,000 year. Because the rock layers do not permit finer dissection of time, the findings are consistent with the extinction being triggered by an impact that happened during "a single bad day. "The mass extinction at the end of the Permian Period was catastrophic and sudden," ravaging sea and land life, Rampino said. "The only thing we know of that can cause an extinction like this is a large impact of an asteroid or comet. But we still havent found conclusive evidence that an impact occurred." The object "would have to be bigger one and a half to twice as big" as the 6-mile- (10-kilometer-) wide asteroid usually blamed for the dinosaurs extinction. A scientist reported finding elevated iridium levels and shocked quartz crystals in Permian-Triassic rocks telltale signs of an impact. "Unfortunately, we have not found a good candidate crater." A comet made of ice "would be almost invisible geologically." Australian scientists said they found a 75-mile- (120-kilometer-) wide crater in western Australia that might be from an impact that caused the Permian-Triassic extinction or a later extinction at the end of the Triassic Period roughly 200 million years ago. The age of that crater is so poorly known that "it is impossible to tie that impact to this [Permian-Triassic] extinction." It is proposed the impact was the cause, perhaps with the impact triggering an undersea release of methane that robbed the oceans of life-sustaining oxygen. He says the impact also may have triggered massive eruptions from volcanic vents named the Siberian Traps. "There is no evidence of an impact" at Permian-Triassic time. "So while the data are consistent with an impact, there is nothing that tells us it was an impact," and massive volcanic eruptions may be a more likely cause. The Siberian volcanic eruptions lasted hundreds of thousands of years, so "if the extinctions were gradual over a half million years, we might suspect volcanism or changes in climate caused by volcanic eruptions. But the fact the extinctions were so sudden and catastrophic argues against a volcanic interpretation." == Similiar enzymes are used for completely different purposes. Are they designed for the functions they occupy, or did evolution just "adopt" whatever came in handy? E.g. blood clotting factors have been found to be relevant in embryonic development in rats, and bacteria and annelid worms use an alpha-hemoglobin for protecting themselves against oxygen. Quite a different function than the one it assumes in vertebrates. Examples like those abound in living organisms. Canoidea The main group, in this case, miacids, which constitute the trunk of the Carnivore tree. Yes, at first there was a mutual divergence between what would become the Feloidea and and Canoidea collections. But within those groups where civets, meerkats and bearcats all look like weasels, pole-cats and coons, (and even bears look like wolverines) there emerged two markedly different lines from their cousins, but which defined the superfamilies of their origin. Dogs diverged from other dog-like animals like bears and sea-lions and cats diverged from civets and genets. == Good mutation in town of Limone Sul Garda, Italy Cardiovascular status of carriers of the apolipoprotein A-I(Milano) mutant: the Limone sul Garda study Sirtori CR, Calabresi L, Franceschini G, Baldassarre D, Amato M, Johansson J, Salvetti M, Monteduro C, Zulli R, Muiesan ML, Agabiti-Rosei E. Circulation 2001 Apr 17;103(15):1949-1954. Center E. Grossi Paoletti, Institute of Pharmacological Sciences, University of Milano, Milan, Italy. cesare.sirtori@unimi.it Review mutation, despite suffering from hypoalphalipoproteinaemia (HA), have a much lower prevalence of atherosclerosis compared to HA control subjects without the apoA1Milano mutation. This indicates that the Milano mutation is highly protective. The apolipoprotein A-IMilano mutation was first described in a family originating from Limone sul Garda in northern Italy. This apoA-I variant shows a single amino acid substitution, arginine 173 to cysteine, and all carriers are heterozygous. The mutation leads to characteristic lipoprotein levels, with very low plasma levels of HDL-C and moderate hypertriglyceridaemia. Despite this atherogenic phenotype the apoA-IMilano mutation is associated with a reduced risk of CVD. To verify the protective status of the apoA1Milano mutation, Sitori and colleagues analysed the incidence of atherosclerosis (using carotid intima thickness) and general CV status of an apoA-IMilano population. == Wallace and Darwin first published on natural selection in the same issue of Annals and Magazine of Natural Science. Wallace has page priority. == Spencer was the fellow who got Darwin to join him on the Jamaica Committee during the Gov. Byre Controversy, a very unpopular position to take. It was a highly principled, anti-racist stand. Darwin, Spencer and Huxley went so far as to attempt to get Gov. Byre prosecuted for murder! And yet this was all in keeping with Darwin's passionate, life-long opposition to slavery and advocacy of the rights of non-Europeans. == Energy to link amino acids is 30 cal/gm. It takes that to get them to react with each other. == Mayr refuses to be convinced by one of the most famous examples of probable sympatric speciation, the apple maggot fly, Rhagoletis pomonella. When domestic apple trees were introduced into the northeastern United States some 150 years ago, a fly that had previously fed on wild hawthorn trees took up residency on the newcomers. One of Darwin's contemporaries, Benjamin Walsh, hypothesized that this adaptive host shift (from hawthorns to apple trees) might be a case of incipient sympatric speciation. In the early 1960s, as a professor at Harvard, Mayr challenged graduate students in his speciation class to prove Walsh wrong. Guy Bush accepted the challenge. "He made it his personal crusade to show that it was possible," says Bush's former graduate student Jeffrey Feder, now a professor at the University of Notre Dame. "At first he was as skeptical as Professor Mayr, but then he realized that if organisms mate in preferred habitats, as Rhagoletis does, sympatric speciation could occur." But Mayr was and remains unconvinced: "The question was, was this a different species? This is where Mr. Bush was never quite able to provide proof. If the process goes on, if it continues for thousands of years, then maybe. But right now, no." In his 1942 book, Mayr went to some length to deny the role of sympatric speciation in the remarkable distribution of cichlids, a family of freshwater fish known for its large numbers of closely related species living together. So, it's perhaps somewhat ironic that today, Mayr cites cichlids as the strongest case for sympatric speciation. Lake Nabugabo in East Africa, for example, is a crater lake that is about a mile-and-a-half long and inhabited by six closely related cichlid species, all of whom could have descended from only a single, common, extant ancestor upstream. "No question about it, that it had to be sympatric speciation," he says. "I am now convinced and this is where I have changed my mind, that there are a lot of cases of sympatric speciation." mportantly, though, even with the cichlids, there seems to be more at play than Darwinian competition for scarce resources. Axel Meyer, University of Konstanz, Germany, explains that in the past, biologists generally thought of speciation as a process occurring over the course of millions of generations. But Lake Nabugabo is an estimated 5,000 to 6,000 years old, and nearby Lake Victoria, with its several hundred cichlid species, all of which are believed to have originated in the lake, is estimated at 200,000 years old. At rates like that, says Meyer, something else must be happening besides the slow, gradual process of evolution by natural selection. The culprit, he believes, is mate choice, also known as sexual selection. Although Darwin wrote about sexual selection, it is not quite how he envisioned the sympatric speciation process. Meyer describes what he calls a eureka "Darwinian moment" while swimming in one of these cichlid-filled lakes. Amazed by the dramatic changes in the male fishes' vivid coloration that he saw as he swam from one part of the lake to another, Meyer realized that mate choice was probably the key to why so many different but closely related species can originate and live together in such a small area. Sexually selected traits, such as bright coloration, tend to evolve more quickly than other features, making them more likely candidates for a sympatric speciation mechanism. A chromosomal rearrangement, or inversion, is another likely candidate. A chromosomal inversion is a physical alteration of a chunk of chromosome, which prevents genes in the inversion from undergoing normal meiotic recombination. The inverted genes effectively evolve in isolation, even as the remaining genome recombines. Eventually, although rather quickly compared to evolutionary rates in other parts of the genome, the isolated genes accrue enough change to drive speciation, even in nonallopatric situations Rieseberg, who studies chromosomal speciation in sunflowers, says that the idea has been around for nearly a century, but only recently have models and evidence become strong enough to convince folks, including Arcadi Navarro, Universitat Pompeu Fabra, Spain, that chromosomal speciation may be widespread. Navarro and University of Edinburgh geneticist Nick Barton recently demonstrated how chromosomal rearrangements may explain speciation processes that separated humans from their closest living relative, the chimpanzee.2 The data, says Navarro, point to the likelihood that the human and chimp lineages diverged even in the presence of limited gene flow. References 1. E. Mayr, Systematics and the Origin of Species, Columbia Press: New York, 1942. 2. A. Navarro, N.H. Barton, "Chromosomal speciation and molecular divergence--accelerated evolution in rearranged chromosomes," Science, 300:321-4, April 11, 2003. == Mitosomes rewrite evolutionary theory Giardia intestinalis possesses highly reduced mitochondria-derived organelles | By David Secko The evolutionary transition from prokaryotes to eukaryotescharacterized by eukaryotic cells obtaining a nucleus and two membrane compartmentsis stillsubject to considerable debate. It has been suggested that a nucleus developed first, followed by the acquisition of mitochondria, a theory that has partly relied on the single-celled eukaryote Giardia intestinalis because it has a nucleus and no mitochondria, suggestive of an intermediate step. The recent identification of mitochondrial remnants in other amitochondrial protists suggests this may not be true. In the November 13 Nature, Jorge Tovar and colleagues at Royal Holloway, University of London report that Giardia intestinalis possesses highly reduced mitochondria remnants called mitosomes (Nature, 426:172-176, November 13, 2003). The work was stimulated by the cloning of a Giardia gene known in other organisms to be involved in the biosynthesis of Fe-S clusters, a critical function of the mitochondria. It was the second such gene to be identified in Giardia (the proteins of which are named IscU and IscS), suggesting the potential for a mitochondrion-derived organelle. Tovar et al. generated antibodies to IscU and IscS and demonstrated that both proteins were present in a high-speed centrifugation pellet containing membranes and membrane-bound organelles, but not in the cytosol. This high-speed sediment was also capable of assembling Fe-S clusters in vitro, signifying the presence of this mitochondrial biosynthetic pathway in the amitochondrial Giardia cells. They then attempted to identify the cellular location of the IscU and IscS. Confocal scanning fluorescence microscopy and anti-IscS and anti-IscU antibodies suggested that the proteins were localized to small cellular structures distributed throughout the cytoplasm. A more detailed view of these structures was provided by immunoelectron microscopy, which localized IscS and IscU to these small organelles and revealed them to be bounded by two limiting membranes, a distinctive feature of mitochondria (since Giardia contains no chloroplast-related biochemistry). Our data provide direct physical evidence for the presence of mitochondrial remnant organelles (mitosomes) in Giardia, as postulated on the basis of previous phylogenetic and biochemical studies, conclude the authors. In an accompanying preview article, Katrin Henze and William Martin from the University of Dusseldorf comment, These findings mark a turning point for views of early eukaryotic and mitochondrial evolution: Giardia's place as an intermediate stage in standard schemes of eukaryotic evolutionary history is no longer tenable. Links for this article W. Martin et al., An overview of endosymbiotic models for the origins of eukaryotes, their ATP-producing organelles (mitochondria and hydrogenosomes), and their heterotrophic lifestyle, Biological Chemistry, 382:1521-1539, November 2001. B.A. Williams et al., A mitochondrial remnant in the microsporidian Trachipleistophora hominis, Nature, 418:865-869, August 22, 2002. [PubMed Abstract] J. Tovar et al., Mitochondrial remnant organelles of Giardia function in iron-sulphur protein maturation, Nature, 426:172-176, November 13, 2003. http://www.nature.com/ Royal Holloway, University of London http://www.rhul.ac.uk/ K. Henze, W. Martin, Essence of mitochondria, Nature, 426:127-128, November 13, 2003. http://www.nature.com/ University of Dusseldorf http://www.uni-duesseldorf.de/ == Cello, J., A.V. Paul, and E. Wimmer. In press. Chemical synthesis of poliovirus cDNA: Generation of infections virus in the absence of natural template. Science. Abstract available at http://www.sciencemag.org/cgi/content/abstract/1072266v1. http://www.sciencenews.org/20020713/fob8.asp American researchers have successfully created all the parts of an artificial virus. They hope to use it to clean up pollution and produce energy. The scientists used commercially available DNA to build an artificial virus from scratch. Its genetic code matches a virus known to infect and kill E. coli bacteria. Phi-X174, a bacteriophage, was created in 14 days. Craig Venter, who backed the Human Genome Project, was one of the lead researchers on the project. Researchers at the Institute of Biological Energy Alternatives in Rockville, Md., performed the experiment. == "The Origins of Order: Self-Organization and Selection in Evolution", by Stuart A. Kauffman. == But let's cover the terminology, which of these *exactly* do you have a problem with or feel uncertain about: Evolution: The observed fact that species change over time. Natural selection: the theory that explains the patterns in evolution we observe. Common descent: The theory that life evolved from a common ancestor (or maybe a small pool thereof). Speciation: The development of a new species. Microevolution/macroevolution (scientific version): Largely discarded terms refering to evolution within a species in the former case and evolution leading to speciation and beyond in the latter. Really, "macroevolution" refered to the supposed special type of evolution that led to speciation. With the realization in the 80's that there was no such process and that ordinary processes led eventually to speciation, the terms have begun to be dropped (with some hint that they may be redefined, scientists hate losing fancy technical terms :-) Microevolution/macroevolution (creationist version): Creationist concepts (evolution we accept, but have to rename because we can't say "evolution" without caveats and evolution we reject) using stolen terms so that they can quote scientists saying one thing and pretend that they mean something else, now used without respect to much of anything except denying that some scale of evolution is valid. The definition of the terms remains as vague as they can possibly arrange. Sympatric speciation: Considered to be the most common mode of speciation through most of the twentith century, where a species slowly shifts into a new species over time. (Sympatric means "same father" if it helps you remember it.) Allopatric speciation: Speciation which occurs in shorter order when a small population is isolated from the main body of the population. (Allopatric means "other father", meaning the species had a seperate birth. == Transitional fossil 1. A fossil displaying characteristics of two species and is a plausible evolutionary intermediate. [den., science] 2. A fossil differing at most by C_max from a known species to be transitional, and at least by C_min from all known species to distinguish it from variety within a known species. C_max < C_min. == "gene" has around six distinct meanings: 1. A hereditable trait (Mendel gene) 2. An evolving character that persists over many generations (evogene) 3. A sequence of DNA 4. A codon 5. An expressed sequence (an exon) 6. A replicator, a high-fidelity copy of anything == Today, whether his critics like it or not, Charles Darwin's thought made possible such once-unimaginable things as organ transplants using organs derived from subhuman species. They work because Darwin was right. That strange thing called ""creation science"" is nothing more than ignorant rantings reflecting a frightened and dying religious mentality. John Shelby Spong, former Episcopal Bishop of Newark, from _Why Christianity Must Change or Die_ == Among the 29 classes of plants are bacteria, blue-green algae, bread mold, mushrooms, dinoflagellates, celular slime molds, etc. These include two different domains (eubacteria and eukarya) and four kingdoms (eubacteria, protista, fungi, and plantae). == Creationists make it seem like gaps are a deep dark secret of paleontology, when just the opposite is the case. I have already noted one of the reasons for the gaps--the low probability of species being fossilized and then discovered. Correlated with this is the growing realization that most species probably arise very rapidly geologically speaking; morphology sometimes does not take as much time to transform as paleontologists once thought. Therefore, if morphological transformations take place over short periods of time (in a geological sense), then the probability of preserving that time interval in the sedimentary record is greatly diminished. Creationists have characterized the evolutionary process as being slow, gradual, and uniform, whereas virtually all modern evolutionary biologists recognize the fact that rates of evolution can be highly variable. Some evolutionary events are apparently extremely rapid so that frequent gaps in the fossil record are to be expected. Nevertheless, numerous examples of morphologically intermediate taxa--transitional forms--have been described from the fossil record, and that record indisputably falsifies the creationist view of the history of life. == http://science.howstuffworks.com/evolution.htm == DNA is made up of four bases -- adenine, cytosine, guanine and thymine -- attached to a sugar-phosphate backbone. Strands of DNA connect to each other when strings of bases pair up -- adenine with thymine, and cytosine with guanine. == What plant exists in more than nine thousand species? Grass. There are more than nine thousand known species in the grass family (technically called "Gramineae"). Many plants you wouldn't think of as grass actually belong to the grass family, including bamboo, rice, sugarcane, corn, rye, wheat, barley, and oats. == Species "Species are systems of populations: the gene exchange between these systems is limited or prevented by a reproductive isolating mechanism or perhaps by a combination of several such mechanisms" (Dobzhansky 1937) Recognition Species Concept (Paterson, 1985) The most inclusive population of biparental organisms which share a common fertilization system. Evolutionary Species Concept (Simpson, 1951) "a lineage (ancestral-descendant sequence of populations) evolving separately from others and with its own unitary evolutionary role and tendencies" == The hyoid (the bone that anchors the larnyx) drops down in the human throat during the middle of the first year of life. The new position prevents breathing and swallowing simultaneously, but allows for the much greater range of sounds needed for speech. It's only with the hyoid in the lower position that human speech is possible == "Scientists have described the bright purple burrowing frog, resembling a fat plum with a white snout, as a "living fossil". It was found in the Western Ghats hills of Kerala, southern India, a region known to be a "hotspot" of biodiversity. DNA analysis showed that the amphibian, Nasikabatrachus sahyadrensis, belonged not only to a previously unknown species but a whole new family of frogs. A total of 29 frog families are known, encompassing more than 4,800 species. The nearest living relatives of N. sahyadrensis are the sooglossids, a small group of frogs found only in the Seychelles in the Indian Ocean. Both have roots stretching back to the Cretaceous period, when dinosaurs such as Tyrannosaurus rex walked the Earth. The frog was described in the journal Nature today by researchers Franky Bossuyt and SD Biju, from the Free University of Brussels in Belgium. They wrote: "Our discovery discloses a lineage that may have been more diverse on Indo-Madagascar in the Cretaceous period, but now only comprises four species on the Seychelles and a sole survivor in India. = Lampreys and other jawless fishes from the Paleozoic are early vertebrates. == Fred Hoyle, the famous british scientist, conveyed the improbability of a living organism emerging "by chance" from a prebiotic soup as about as likely as ......"a tornado sweeping through a junkyard causing the assembly of a functioning Boeing 747 from the scrap materials therein". False analogy. Scrap in a junkyard doesn't have any mechanism like mutation, sexual recombination, natural selection or genetic inheritance.There is no self organizing capacity. How could something be LESS like biological evolution. == Van Valen L. (1973): "A New Evolutionary Law", Evolutionary Theory Ernst Mayr's "What Evolution Is" Simon Conway Morris "Life's Solution: Inevitable Humans in a Lonely Unvierse", Cambridge University Press. == http://www.sciencemag.org/cgi/content/full/299/5608/825a "Some species such as the mole Talpa europaea and wood mouse Apodemus sylvaticus have fossil records that extend as far back as the Early Middle Pleistocene No fossolized (mineralized or permineralized!) mole has been found that is younger than 2.5 million years. == Darwin himself used "descent with modification," and didn't adopt Herbert Spencer's term "survival of the fittest" until a later book == Sure Darwinism lacks validity - that's why I'm an evolutionist. Darwinism is a term created by creationists to turn evolution into the cult around a person. Darwin was wrong about many things but the essense of his ideas have survived more trials then the majority of scientific ideas you have no problems accepting. == A human protein called apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G (APOBEC3G for short) defends cells against retroviral infection by triggering hypermutation in RNA during reverse transcription, scrambling the viral genes by changing G's to A's. HIV, however, can counter the effects of APOBEC3G with a protein called virion infectivity factor, Vif. Sounds like another evolutionary arms race... either that, or it certainly was nice of that Intelligent Designer to give us an ingenious defense against viruses and then give the viruses an even more ingenious way to outwit that defense. == The first land colonising fish is Eusthenepteron. == Crocs share one reptilian feature--gender is determined by incubation temperature. The four-chambererd heart is not complete in the croc. The septum is partial, but with a valve. A croc can make a four-chambered heart for spurts of high activity, but must revert afterwards. It is not endothermic. == modern chimpanzees (Pan troglodytes) bonobos(Pan paniscus), == Eldredge N. & Gould SJ. 1972. Punctuated equilibria: an alternative to phyletic gradualism. In T.J.M. Schopf (ed), Models in Paleobiology pp. 82-115. Freeman, Cooper and Co., San Francisco. You will also find the paper reproduced in: Eldredge, N. 1985. Time Frames: the Rethinking of Darwinian Evolution and the Theory of Punctuated Equilibria. Simon and Schuster, New York (pp. 193-223) 1.Evolution Now: A Century After Darwin, ed. John Maynard Smith, (1982), p. 140 "The Ediacaran Experiment", Natural History, 93(2):14-23, Feb. 1984 American Journal of Physical Anthropology Journal of Human Evolution == Ridley latest book, "Nature via Nurture, == Paul and her colleagues used chemical techniques to produce large segments of DNA corresponding to portions of the polio virus. They made one segment themselves, then ordered the rest from a company that routinely machine-generates DNA. Once they had all the segments, the team pasted the pieces together to produce one long stretch of DNA. They then used a commercially available enzyme to convert the DNA into RNA - the genetic form of the polio virus. Finally, they added the RNA to a soup made from human cells. This enabled the RNA to use the cellular machinery to create the proteins that complete the virus particles. The result was an infectious agent that could destroy cultured human cells and paralyse or kill mice in much the same way as the normal polio virus. Journal reference: Science (DOI: 10.1126/science.1072266) [1] Unrau PJ, and Bartel DP, RNA-catalysed nucleotide synthesis. Nature, 395: 260-3, 1998 [2] Orgel LE, Polymerization on the rocks: theoretical introduction. Orig Life Evol Biosph, 28: 227-34, 1998 [3] Otsuka J and Nozawa Y. Self-reproducing system can behave as Maxwell's demon: theoretical illustration under prebiotic conditions. J Theor Biol, 194, 205-221, 1998 [4] Woese C, The universal ancestor. Proc Natl Acad Sci USA, 95: 6854-6859. [5] Varetto L, Studying artificial life with a molecular automaton. J Theor Biol, 193: 257-85, 1998 [6] Wiegand TW, Janssen RC, and Eaton BE, Selection of RNA amide synthases. Chem Biol, 4: 675-83, 1997 [7] Severin K, Lee DH, Kennan AJ, and Ghadiri MR, A synthetic peptide ligase. Nature, 389: 706-9, 1997 [8] Ruse M, The origin of life, philosophical perspectives. J Theor Biol, 187: 473-482, 1997 [9] Lee DH, Severin K, Yokobayashi Y, and Ghadiri MR, Emergence of symbiosis in peptide self-replication through a hypercyclic network. Nature, 390: 591-4, 1997 [10] Lee DH, Severin K, and Ghadri MR. Autocatalytic networks: the transition from molecular self-replication to molecular ecosystems. Curr Opinion Chem Biol, 1, 491-496, 1997 [11] Di Giulio M, On the RNA world: evidence in favor of an early ribonucleopeptide world. J Mol Evol, 45: 571-8, 1997 [12] Ekland EH, and Bartel DP, RNA-catalysed RNA polymerization using nucleoside triphosphates. Nature, 383: 192, 1996 [13] Lohse PA, and Szostak JW, Ribozyme-catalysed amino-acid transfer reactions. Nature, 381: 442-4, 1996 [14] Ferris JP, Hill AR Jr, Liu R, and Orgel LE, Synthesis of long prebiotic oligomers on mineral surfaces [see comments]. Nature, 381: 59-61, 1996 [15] Lazcano A, and Miller SL, The origin and early evolution of life: prebiotic chemistry, the pre- RNA world, and time. Cell, 85: 793-8, 1996 [16] Ertem G, and Ferris JP, Synthesis of RNA oligomers on heterogeneous templates. Nature, 379: 238-40, 1996 [17] Lee DH, Granja JR, Martinez JA, Severin K, and Ghadri MR, A self-replicating peptide. Nature, 382: 525-8, 1996 [18] Joyce GF, Building the RNA world. Ribozymes. Curr Biol, 6: 965-7, 1996 [19] Ishizaka M, Ohshima Y, and Tani T, Isolation of active ribozymes from an RNA pool of random sequences using an anchored substrate RNA. Biochem Biophys Res Commun, 214: 403-9, 1995 [20] Mushegian AR and Koonin, EV, A minimal gene set for cellular life derived by comparison of complete bacterial genomes. Proc. Natl. Acad. Sci. USA, 93: 10268-10273. [21] Ekland EH, Szostak JW, and Bartel DP, Structurally complex and highly active RNA ligases derived from random RNA sequences. Science, 269: 364-70, 1995 [22] Breaker RR, and Joyce GF, Emergence of a replicating species from an in vitro RNA evolution reaction.Proc Natl Acad Sci U S A, 91: 6093-7, 1994 [23] Chyba C and Sagan C, Endogenous production, exogenous delivery and impact-shock synthesis of organic molecules: an inventory for the origins of life. Nature, 355: 125-32., 1992 [24] Doudna JA, Couture S, and Szostak JW, A multisubunit ribozyme that is a catalyst of and template for complementary strand RNA synthesis. Science, 251: 1605-8, 1991 [25] Lahav N, Prebiotic co-evolution of self-replication and translation or RNA world? J Theor Biol, 151: 531-9, 1991 [26] Stadler PF, Dynamics of autocatalytic reaction networks. IV: Inhomogeneous replicator networks. Biosystems, 26: 1-19, 1991 [27] Eigen M, Gardiner W, Schuster P, and Winkler-Oswatitsch R, The origin of genetic information. Sci Am, 244: 88-92, 96, et passim, 1981 [28] Eigen M, and Schuster P, The hypercycle. A principle of natural self-organization. Springer-Verlag, isbn 3-540-09293, 1979 [29] Yockey HP, On the information content of cytochrome c. J Theor Biol, 67: 345-76, 1977 Statistics at Square One, T.D.V. Swinscow, 8th Edition Paperback, Published by Amer College of Physicians, 1983, ISBN: 0727901753 Evolution from Space, F Hoyle and Wickramasinghe, JM Dent and sons, London, 1981 Vital Dust: Life As a Cosmic Imperative, by Christian De Duve, Basic Books 1995, ISBN: 0465090451 The Major Transitions in Evolution, Maynard Smith J & Szathmary E, 1995, WH Freeman, ISBN: 0716745259 The Origins of Order: Self Organization and Selection in Evolution. By Stuart Kauffman, S. A. (1993) Oxford University Press, NY, ISBN: 0195079515. == The forelimbs in vertebrates develop from different body segments in different species. In the newt, they develop from trunk segments 2, 3, 4 and 5; in the lizard from segments 6, 7, 8 and 9; and in humans from segments 13, 14, 15, 16, 17 and 18. If the optic cup is removed in one species of frog the eye lens will not develop, while in another species the lens does develop. It cannot be doubted that the lenses of these two species are homologous, yet they differ completely in their mechanism of determination and differentiation. The the protein that determines "front" and "back" in limb development works exactly the same way for chickens as it does for mammals Every four-footed vertebrate animal has a five-fingered design with the same set of bones in modified form. Those of the arm, wrist and hand that are in humans, can also be found in modified form in all == None of the following modern mammals are found below the Cenozoic: Antelop, Bats, Cats, Deer, Dolphins, Elephants, Giraffes,Hominids,Horses,Kangaroos Mice,Pigs,Porcupines,Primates,Rabbits,Rats, Rhinos, Shrews, Whales, Zebras == http://www.cs.colorado.edu/~lindsay/creation/fossil_series.html speciation == If you bothered to read the actual scientific literature, which is, afterall, where scientists publish, you would see that they are not at all shy about voicing and debating uncertainties. But of course those uncertainties tend to be at a much more detailed and esoteric level than the average creationist can even imagine, let alone be conversant in. They are not at all at the level of there being a 'fundamental problem with the basics of evolutionary theory', which creationists often suggest. == Before a life form can be considered a valid new genus or species, it must be deposited in two separate International Collections of Microorganisms and a scientific paper describing all new features of the organism must be either published in the International Journal of Systematic and Evolutionary Microbiology or, if published in another journal, it must be verified by the International Committee on Systematics of Prokaryotes (ICSP), the clearinghouse for bacterial species. Once a microbe is finally accepted as a valid new species, says Hoover, the years of intense labwork and wallowing in smelly lake mud suddenly become worthwhile. The Goldilocks Zone gets a little bigger. And life "out there seems more likely than ever. == We know little about the time frame for the origin of life. It's often claimed that it couldn't have arisen earlier than about 4bya, because cosmic bombardment was too intense till then for there to be a solid surface on earth. And the oldest indications that life might have been present (chemical fossils of a sort) are around 3.8bya. Even if we believe those two numbers, that allows 200my for the origin of life. == Prions are not really life. Prions are proteins arrange themselves according to the laws of chemistry. One prion form can initiate a change in crystal structure in other prions. (This can lead to BSE, CJD etc where the aberrant form causes the standard form to reform in the aberrant form). == Consider protein racemerization. The universality of the stereoisomers in earth life was seen as an anomaly for decades. Scientists did research, discovered that polarized light could account for the bias, noted it would have been common in the early solar system, predicted that if this was the case, stereoisomers in asteroids and other places without life would show the same bias, checked, and confirmed the prediction. Clays also can select one variety of amino acids over the other variety. == If you do research based on ribosomal RNA you get a tree with three main branches from the root. The three branches are bacteria, archaea and eukarya. All of the organisms closest to the bottom of their branches, i.e. nearer the last common ancestor, are thermophiles or hyperthermophiles. That is they live in environments that are hot. == Koestler Midwife Toad Fraud in science == Think about those many anestors everbody has: Not a single one of them died in childbirth. Not a single one died young. Not a single one was infertile. Every single one lived long enough to multiply. That is a truly amazing population, your ancestors. "The world becomes full of organisms that have what it takes to become ancestors. That, in a sentence, is Darwinism." Richard Dawkins, _River out of Eden_, London: Weidenfeld and Nicholson, == Ernst Mayr genetic revolutions in allopatry" 1942 _Systematics and the Origin of Species_, Mayr, E 1954 _Change of Genetic Environment and Evolution_. == A contribution to a solution was provided in my 1954 paper on speciational evolution. I proposes that a peripherally isolated founder population could undertake considerable ecological shift and genetic restructuring and become the ideal starting point for a new phylogenetic lineage. It is highly unlikely that such a small population would be preserved in the fossil record, however. This theory of geographic speciation was adopted and elaborated by Eldredge and Gould (1972) ... _This is Biology_ p 70 The ref is "Change of genetic environment and evolution_ in J Huxley, A Hardy and E Ford eds, _Evolution as a prcoess_, pp157-180. == We have a lot of evidence that gene duplication happened and that the genes diverged. When the ancestor of all vertebrates duplicated its genome and became either tetraploid or allotetraploid all the genes were duplicated. Some like the melanocortins were duplicated before this event and we can see linkage between the duplicated genes on the various chromosomes. A lot of the duplicated genes have been lost, but we can see the ancient syntenic groups and which chromosomes used to be homologous to each other, but have diverged into different diploid chromosomes. The evidence is that even though we have duplicated genes that do different things on different chromosomes the duplicats are linked to the same genes. When a genome doubles you get two sets of nearly identical chromosomes. The two sets then diverge, but closely linked genes tend to stay together and in many instances we can see that even though we call them different chromosomes today they were obviously the same chromosome in the past because they share the same duplicated gene sets. It is just that the duplicated genes do something different now. Maize (corn) is an excellent example of this. You can clearly see that two different genomes combined to form an amphidiploid (allotetraploid two chromosomes from one species and two chrmosomes from another). The two genomes have mixed by chromosome fusion and rearrangements, but the event was recent enough that we don't have as much trouble differentiating the two genomes involved. Gene duplication isn't just some thrown up explanation, it is the only reasonable explanation of the data that we have. == Capuchin monkeys are among the few primates along with men and chimpanzees that hunt cooperatively. == Adrian Desmond... 'Huxley: From Devil's disciple to Evolutions' High Priest' == Scientists have found fossils of what they say is the largest rodent that ever lived, a 9-foot-long, buffalo-size creature with a long tail and powerful teeth that foraged along the riverbanks of Venezuela about 8 million years ago. Scientists said Phoberomys pattersoni probably weighed up to 1,545 pounds, about 10 times the size of today's largest rodent, the South American capybara. But Sanchez-Villagra said that among rodents, a huge mammalian order that includes field mice, hamsters, squirrels, beavers and chinchillas, Phoberomys is most closely akin to the pacarana a rare, 33-pound foraging animal from the western reaches of the Amazon jungle. "The environment was very diverse," Sanchez-Villagra said. "There were lagoons and forested areas very near the seashore and fauna from a large river," probably connected to today's Orinoco, which flows east from the Amazon. Urumaco sits on the site of an old oilfield where a petroleum geologist in 1952 discovered a rock layer rich in fossils especially of turtles, crocodiles and other reptiles. Zoologist Roger Wood, then a Harvard graduate student, saw the exhibits at Venezuela's Central University in 1970 and enlisted the university's help in mounting an expedition with his world-renowned mentor, Harvard mammalogist Bryan Patterson. The expedition yielded spectacular reptile finds, including several huge crocodile species and a turtle shell 812 feet long still the largest ever found: "We didn't find much in the way of mammals," said Wood, a teacher at New Jersey's Richard Stockton College, but a later expedition unearthed several teeth from a very large mammal. Investigators named it Phoberomys pattersoni, in honor of Patterson, who died in 1979. Phoberomys had much heavier hind legs than front legs, indicating a relative lack of speed, and large, strong teeth for grinding grass, leaves and other swamp vegetation that probably made up its diet. Unlike other continents, where rodents competed for food and habitat with other small, aggressive mammals, South America offered few rivals for millions of years, so rodents "went berserk," he said. Urumaco presented a major opportunity to expand knowledge of the continent, for the 8 million-year-old deposit was relatively close to the spot where Earth's restless crust brought Pacific islands ashore 3 million years ago to form the land bridge that would link the two Americas. "When it happened, there was a huge, intense exchange of fauna," Sanchez-Villagra said. "There was a lot of extinction on both sides," although the disappearance of Phoberomys remains a mystery: "One likely reason for extinction is climate change. This area was forest, swampy, full of vegetation, and 8 million years later it's a desert." As for predators, "it's very difficult to tell what happened," he added. "It's an arms race. If you get too large, nobody can eat you. On the other hand, the predators are also getting larger." Fleagle noted that the Central American isthmus turned out to be a boon for some southern animals moving north such as the armadillo and the sloth, but maybe not for others, such as Phoberomys, who stayed put. "Who knows what happened," said Fleagle, noting that the land bridge allowed jaguars, bears and other predators to head south. "A jaguar's used to running down horses and camels in North America, and now there's all these dumb animals, like giant rodents, who have never seen him before." == What caused the worst mass extinction in Earth's history 251 million years ago? This event is one of the most catastrophic in life's history: the P/T extinction. An asteroid or comet colliding with Earth? A greenhouse effect? Volcanic eruptions in Siberia? Or an entirely different culprit? Scientists have suggested many possible causes for this "Great Dying": severe volcanism, a nearby supernova, environmental changes wrought by the formation of a super-continent, the devastating impact of a large asteroid -- or some combination of these. Whatever happened during this period left no form of life undisturbed: No class or species was spared from devastation. Trees, plants, lizards, proto-mammals, insects, fish, mollusks, and microbes -- all were nearly wiped out. More than 9 in 10 marine species and 7 in 10 land species vanished. Life on our planet almost came to an end. == A human embryo of six and eight months old is covered with thin fur. Sometimes, prematurely born infants have fur all over their bodies. == The scientist pay attention to small insects called human body lice and the role that they played in the evolution of a homo sapiens, when primeval humans started wearing clothes. Clothes mean a lot more to body lice than to fashionable women, because insects lay eggs in clothes. The genetic analysis of the insect showed, lice are 70,000 years old, they appeared soon after human beings started resettling from Africa to Europe, where they had to wear clothes because of the cold. Dr Stoneking's team is going to study the "molecular clock" in the DNA of human body lice (insects die in another environment in 24 hours). The research will allow to find the mutation speed and human evolution stages. There are three kinds of human lice- head, body and pubic lice. == Some people think that the "higher" animals, like mammals and birds, and especially humans, are somehow more evolved than lower organisms, like bacteria. Anything on this earth right now has been evolving for the same amount of time, so really, each species is as evolved as each other species. There are countless different climates, food sources, and other factors, and there are countless ways to deal with each of these factors, any animal that can take advantage of these can theoretically survive and pass on it's genes. == The platypus shares all the characteristics listed for echidna, and has the added distinction of being one of only two venomous mammals. The other venemous mammal is the short tail shrew...its venom is very similar to that of a cobra. == Genes are selected, especially those that produce a favorable phenotype. Behavior and environment can influence phenotype. Thus behavior and environment may be key to what genes are selected. == SPECIES NOUN: 1. Biology a. A fundamental category of taxonomic classification, ranking below a genus or subgenus and consisting of related organisms capable of interbreeding. See table at taxonomy. b. An organism belonging to such a category, represented in binomial nomenclature by an uncapitalized Latin adjective or noun following a capitalized genus name, as in Ananas comosus, the pineapple, and Equus caballus, the horse. == Evolution Journal http://whittlebit.com/visitpage.php?url=http://lsvl.la.asu.edu/evolution/ == The chimp 2p and 2q chromosomes are fused in the human #2. The telomeres are even still there in the middle. As is the remnant of one of the centromeres (the other being still an active centromere). == Watson, J. D. & Crick, F. H. C. 1953. Molecular structure of Nucleic Acids. Nature 171: 737-738. Mullis, K.B. (1990). The unusual origin of the polymerase chain reaction. Scientific American 262: 56-65. == Sharp-tailed and sage grouse interbreed.There are a number of species that are so closely related(athough they are listed as separate species)that they interbreed and produce fertile, perfectly "functional" offspring. "Western gulls"(Larus occidentalis) x "glaucous-winged" gulls(Larus glaucescens), for instance. These hybrids exist in considerable numbers and the phenomenon is well-known. == A source of evidence is the fossil record of hominoid evolution, which shows significant growth in brain size for several million years without a corresponding increase in the use of either language or tools. Then suddenly (in evolutionary time), the distinctively human traits of language, symbols and tools appeared. Devlin argues that our ancestors' increase in brain size was driven not by acquisition of language but by the selective advantage conferred by a richer understanding of relationships among objects in the physical environment and in an increasingly complex social world. Once the brain reached sufficient size and complexity, it rather quickly developed the capacity for what Devlin calls "off-line" or "what-if" thinkingthe capacity to reason hypothetically about relationships and abstractions that undergirds both language and mathematics. == Genetic barriers are not yes/no structures. Consider the case with ring species, such as the terrapins that live on the beaches of Florida. If you started at the tip of the Florida Panhandle, and walked over the beaches all the way to the Georgia border on the other side, you would find that the visual appearance of the terrapins (land-based, salt-water tolerant turtles) changed over the length of your walk. Scientists divide them into a number of subspecies, but the lines are very blurry. However, the interesting thing here is that each subspecies is fully capable of breeding with it's geographically contiguous subspecies, and is usually capable of breeding (with decreased success) with subsequent geographic groups, if given the opportunity (usually, this will be artificial, since they don't naturally wander that much). However, the further apart two subspecies are, the less they will be able to interbreed until distant groups are completely incompatible. So, despite the fact that breeding is contiguous from one end to the other, and thus they must all be the same species, the animals on either end of the range cannot interbreed and so would count as different species. Being classified as a separate species is, in any case, often an arbitrary judgment call when two popularions are closely related. I know this because I'm familiar with "Puget Sound gulls", who generally are hybrids or backcrosses between "Western" gulls(Larus occidentalis) and "glaucous winged" gulls(Larus glaucescens), although seemingly "pure" varieties can be seen --- but these may just *look* one or the other of the parent species and be hybrids anyway. Not only that, but "glaucous winged" gulls and "herring" gulls interbreed in Western Alaska(among other places, and there are other fairly common gull "species crossings". This is *extremely* well-known. Evolution is not only a constant process, it is a messy one; species aren't neat little boxes from which nothing in the box ever escapes. Otherwise evolution would never toake place. == Some recent ancestors of dogs: * Cynodictis (late Eocene) -- First known arctoid (undifferentiated "" dog/bear). * Hesperocyon (early Oligocene) -- A later arctoid. Compared to miacids like Paroodectes, limbs have elongated, carnassials are more evolution can be traced in North America, with bears branching out into a Holarctic distribution. * Cynodesmus (Miocene) -- First true dog. The dog lineage continued through Tomarctus (Pliocene) to the modern dogs, wolves, & foxes, Canis (Pleistocene). == Evolution evidence 1. Similarity of MA skull to A. afarensis skull. 2. MA MtDNA clusters within the chimps. 3. A. afarensis was an upright walker. == Mustard, turnips, and rutabagas are of the same genus as cabbage === When we look at an enzyme like RNASE1B,we find a gene duplication was at work. == The first multicelled animals (metazoans) developed simple nervous systems about 560 million years ago. == Hyla chrysoscelis and Hyla versicolor grey tree frogs, from the eastern US, are identical in appearance -- they cannot be told apart in the field and can only be identified by a chromosome count in the lab. The sperm from one cannot fertilize the other. Thus, they are different species. Domestic wheat is descended from wild emmer grass. The pollen from domestic wheat cannot fertilize the ovum of emmer grass. == Define "species" Species are expected often to have fuzzy and imprecise boundaries because evolution is ongoing. Some species are in the process of forming; others are recently formed and still difficult to interpret. == Exploring, from an evolutionary point of view, the potential for major problems from a new class of antibiotics. Graham Bell and Pierre-Henri Gouyon Arming the Enemy: The Evolution of Resistance to Self-Proteins Microbiology 149 (2003) 1367-1375 DOI 10.1099/mic.0.26265-0 == Evolution is a fact. There is a theory of evolution which explains the observed changes in life forms over time on earth. Your test shows that you don't understand what evolution is. Evolution is the change that occurs over time in populations. There is no goal. There is no intent, except that life forms intend to continue living. Sometimes the ones that have the most descendants are the ones that are a bit different from their ancestors. == New answers to these questions come from a study of leaf-eating monkeys by researchers at the University of Michigan, the National Institutes of Health, and the Chinese Academy of Sciences. In the work, published online March 4 by Nature Genetics, U-M's Jianzhi Zhang and colleagues show how a duplicated copy of a gene encoding a pancreatic enzyme has evolved to help the monkeys cope with an unusual diet. == Hans Thewissen? One of the world'sforemost experts on the subject. Featured in the November 2001 issue of National Geographic, "The Evolution of Whales". http://darla.neoucom.edu/DEPTS/ANAT/whaleorigins.htm = The Unboilable Bug Summary: Long thought to be impossible, a single-celled microbe has been found to thrive above the boiling temperature of water. The record-holder, called 'Strain 121', is part of a class of extreme lifeforms, but surviving a top temperature of 250 degrees Fahrenheit takes this discovery into a class of its own. The Unboilable Bug based on National Science Foundation report It may be small, its habitat harsh, but a newly discovered single-celled microbe leads the hottest existence known to science. Its discoverers have preliminarily named the roughly micron-wide speck "Strain 121" for the top temperature at which it survives: 121 degrees Celsius, or about 250 degrees Fahrenheit. A "black smoker" vents atop a 10-meter-high chimney, with an internal temperature of 342 C Credit: Pacific Marine Environmental Laboratory, NOAA Announcing Strain 121's record-breaking ability to take the heat in the August 15 issue of the journal Science, researchers Derek Lovley and Kazem Kashefi write, "The upper temperature limit for life is a key parameter for delimiting when and where life might have evolved on a hot, early Earth; the depth to which life exists in the Earth's subsurface; and the potential for life in hot, extraterrestrial environments." Previously, the upper known temperature limit for life had been 113 C (235 F), a record held by another hyperthermophilic--or extreme-heat-liking -- microbe called Pyrolobus fumarii. The work by Lovley and Kashefi, researchers at the University of Massachusetts, Amherst, was supported by the National Science Foundation's Life in Extreme Environments program. Their NSF project may also yield clues to the formation of important ore deposits, the remediation of toxic contaminants, and more efficient recovery from petroleum reserves. Magnetite (attracted to the magnet), the byproduct of Strain 121's respiration of iron oxide, offers a tell-tale sign of life in the left tube, compared to the uninoculated tube on the right. On a standard stovetop, water boils at 100 C, or 212 degrees F. Strain 121, however, comes from water at the ocean bottom, from a surreal deep-sea realm of hydrothermal vents. Heated to extremes by the earth's magma, water there spouts forth through leaks in the ocean floor. The pressure of the immense depths prevents such hot water from turning to steam--even as it sometimes emerges at temperatures near 400 C (750 F). The sample cultured by Lovley and Kashefi was collected about 200 miles offshore from Puget Sound and nearly a mile and a half deep in the Pacific Ocean by a University of Washington team led by biological oceanographer John Baross. A thin section of Strain 121 illustrates its single-layer cell envelope (S) and cytoplasmic membrane (CM). Baross's crew, also supported by NSF, used a remotely operated submarine to retrieve it from the Pacific Ocean's Juan de Fuca Ridge, a lightless seascape where vents called "black smokers" rise up like three- and four-story chimneys and continuously spew a blackening brew laced with iron and sulfur compounds. The neighborhood is called Faulty Towers. While suffocating, crushing, scalding, toxic and downright abysmal by most living standards, the arrangement is not so bad for Strain 121 and its ilk. They are archaea, single-celled microbes similar to, but not quite, bacteria. They often live amid extreme heat, cold, pressure, salinity, alkalinity, and/or acidity. Archaea literally means "ancient," and Lovley and other biologists tend to call them "deep branchers" because these microbes were among the first branches on the "tree of life." According to Lovley, Strain 121--it will be given a species name after his lab finalizes the microbe's description-uses iron the way aerobic animals use oxygen. "It's a novel form of respiration," Lovley says, explaining how Strain 121 uses iron to accept electrons. (Many archaea also use sulfur). As oxygen does in humans, the iron allows the microbe to burn its food for energy. Chemically, the respiration process reduces ferric iron to ferrous iron and forms the mineral magnetite. The presence of vast deposits of magnetite deep in the ocean, its presence as a respiratory byproduct of some archaea, and the abundance of iron on Earth before life began all led Lovley and Kashefi to write that "electron transport to ferrous iron may have been the first form of microbial respiration as life evolved on a hot, early Earth." The researchers tested the process with Strain 121 cultures kept at 100 C in oxygen-free test tubes. "It really isn't technically difficult. You just need some ovens to get it hot enough--and remember not to pick it up with your bare hands," Lovley says, speaking from experience. They discovered that Strain 121 grew at temperatures from 85-121 C (185-250 F). (Meanwhile, Pyrolobus fumarii, the former top-temperature record-holder, wilted. After an hour at 121 C, only 1 percent of its cells were intact and none appeared viable). "Growth at 121 C is remarkable," report Lovley and Kashefi, "because sterilization at 121 C, typically in pressurized autoclaves to maintain water in a liquid state, is a standard procedure, shown to kill all previously described microorganisms and heat-resistant spores." Not only did Strain 121 survive such autoclaving, its population doubled in 24 hours at such heat and pressure. While they could not detect growth at higher temperatures, the researchers found that cultures that spent two hours at 130 C (266 F) still grew when transferred to a fresh medium at 103 C (217 F), with each new single-celled member appearing like a tiny tennis ball filled with cytoplasm and covered with about a dozen whip-like flagella. == Genome Hunt Shows We're Closer to Rats Than Cats A comparison of human DNA to 12 other animals shows we share more than our genes and helps show that people are more closely related to rats than to cats, U.S. scientists reported on Wednesday. The survey also adds to the argument that so-called ``junk'' DNA is nothing of the sort, but must do something important because it stays virtually identical across many species. It also supports what is becoming increasingly clear -- that the stretches of DNA we call genes are only a small part of the genetic story. The research team at the National Human Genome Research Institute and several universities compared the same stretch of DNA in a chimpanzee, baboon, cat, dog, cow, pig, rat, mouse, chicken, zebrafish and two species of pufferfish - Fugu and Tetraodon -- with human DNA. In people, this stretch of DNA it is a much-studied genetic region that contains the CFTR gene that, when mutated, causes cystic fibrosis. "It provides some pretty definitive evidence that we are indeed closer to rodents than we are to carnivores,'' "Our data really puts the nail in the case. In the sequence you can find changes in the genome that clearly occurred in both humans and rodents but did not occur in others.'' The changes come in repetitive sequences of DNA that, until just a few years ago, were believed to be junk -- useless stretches of trash that somehow got saved. DNA is very difficult to interpret. Its long, long code is built on just four nucleotides -- the compounds known by the abbreviations A,C,T and G. Reading the long string of four letters repeating in various combinations is proving to be even trickier than scientists thought it would be. At first they believed the genes -- the sequences that control production of the protein building blocks of the body -- would be the only functioning parts of the sequence. But it turns out there are sequences that control the genes, and perhaps that "It now seems that about 5 percent of our genomes are functionally important is"functionally important is notencoding DNA. We don't even know what it looks like so how are we going to find it?'' "This is the idea that you can truly use sequences from multiple genomes and analyze them all at once to try and find the small percent that is shared among all of them" "We believe this is going to be a very valuable way to find those sequences that are very important.'' Why? Because nature cannot ditch vital DNA. "Evolution is about mixing things up. If evolution has hung on to some stretch (of DNA), even if it is repetitive, it is telling us something ... Where did (evolution) find it wasn't safe to change the genome?'' he asked. Scientists will look at 100 different regions of the genomes of the 13 species. This is the first region they have analyzed, they reported in Thursday's issue of the journal Nature. "We will discover new types of functional elements in the coding DNA that we didn't even know existed." == The fossils of 511 year old crabs have been found in England. They are the oldest crustaceans ever found,discovered in limestone near Wales. Each is about a half millimeter long but soft tissues have been preserved in great detail. Each has ashell,antenna and appendages typical of crustaceans. == More important than the problems which exist with evolution, there are these facts, random genetic changes happen, selection and neutral drift happen, divergence of function and changes in morphology happen, extinctions happen, drastic changes in environment and ecology happen, and have been happening for billions of years. == The evidence we have, from many lines not just fossils, shows common descent. We will always have something missing, very few organisms fossilize. We posit that each step was done by reproduction. We can't provide fossils for each step, but that is not a surprise. Very few organism fossilize. Of those that do, we mostly have hard shelled marine organisms. Luckily we have several other lines of evidence all pointing to common descent. == "Evolution is what happens to imperfect replicators" (Dawkins) == here are hybridized green sea turtles and hawksbill turtles, as well as some hybrids of Borneo and Sumatran orangutans. == http://www.talkorigins.org/faqs/faq-transitional.html http://www.holysmoke.org/sdhok/transfos.htm http://www.origins.tv/darwin/transitionals.htm http://www.talkorigins.org/faqs/faq-transitional/part1a.html#amph1 http://www.talkorigins.org/faqs/faq-transitional/part1b.html#bird http://www.talkorigins.org/faqs/faq-transitional/part1b.html#mamm == All use a form of retinol as a starting point, but retinol is easily derived (by two steps) from vitA, which is used in all life forms for other purposes. After the first two steps, the way that the absorption of photons get converted to neural signals in vertebrates and invertebrates is quite different. == Stephen J. Gould said this "Since we proposed punctuated equilibria to explain trends, it is infuriating to be quoted again and again by creationists -- whether through design or stupidity, I do not know -- as admitting that the fossil record includes no transitional forms. The punctuations occur at the level of species; directional trends (on the staircase model) are rife at the higher level of transitions within major groups. [Stephen Jay Gould, Evolution as Fact and Theory Science and Creationism, (New York: Oxford University Press, 1984), p. 124.]" ======= from apes to men. Sahelanthropus tchadensis (320380cc), ca. 6-7mya. Ardipithecus ramidus (dental and postcranial remains), ca. 5-6mya. Orrorin turgenesis (postcranial), ca. 5mya. Australopithecus anamensis (cranial capacity unknown), ca. 4.9-5.2mya. A. afarensis (mean of 470cc, range 375-540cc), ca. 3.8-2.8mya. A. bahrelghazali (cranial capacity unknown), ca. 2.8-3.2mya. A. africanus (440-480cc), ca. 2.2-2.6mya. A. garhi (c. 450cc), ca. 2.3-2.6mya. A. robustus (c. 475cc), ca. 1.4-1.8mya. A. boisei (c. 450cc), ca. 1.2-1.8mya. A. aethiopicus (c. 410cc), ca. 2-2.4mya. H. habilis (c. 500-800cc), ca. 1.8-2.1mya. H. ergaster (c. 1100-1434), ca. 1.3-1.8mya. H. erectus (c. 725-1250cc), ca.250kya. - 1.3mya. H. heidelbergensis (c. 1300cc), ca. 300-170kya H. neanderthalensis (c. 1350-1600cc), ca. 200-35kya. H. sapiens (c.1300-1500cc), ca. 170kya-present http://www.theistic-evolution.com/transitional.html http://www.cs.colorado.edu/~lindsay/creation/fossil_series.html -- Overview of the 3.8 billion year fossil record: first bacteria before first multicellular organism before first shelled organisms before first insects before first amphibians before first reptiles before first dinosaurs before first birds before first placental mammals before first first apes before first hominids. fishes to amphibians, Eusthenopteron, Icthyostega and Acanthastega fill that role amphibians to reptiles, Seymouria reptiles to birds Archaeopteryx, as well as the recently discovered feathered dinosaurs. Microraptor Gui is especially interesting. Archaeopteryx also has teeth, unfused tibia and fibula, a four-toed foot, a long bony tail and abdominal ribs which were ALL characteristics of small theropod dinosaurs. Charig, A. J., Greenaway, F., Milner, A. C., Walker, C. A., & Whybrow, P. J. 1986. _Archaeopteryx_ Is Not a Forgery. Science 232:622-626. Shipman, P. 1989. Sixth Find is a Feathered Friend. Discover (January 1989):63. reptiles to mammals The Therapsids. http://www.asa3.org/ASA/resources/Miller.html great article on fossils http://www.talkorigins.org/faqs/horses/horse_evol.html Horse evolution: Orohippus before Epihippus (4 toes) before Mesohippus (3 toes) before Miohippus before Parahippus before Merychippus (2big 1small toes)before Pliohippus (1 toe) before Equus (modern horses) pictures http://chem.tufts.edu/science/evolution/HorseEvolution.htm == _Eoraptor_ is fully bipedal. The earlier _Lagosuchus_ was fully bipedal, and most experts don't even think it was a dinosaur at all, although it's at least close to the line dividing theropods from basal archosaurs. Even _Euparkeria_, an earlier more primitive basal archosaur, was largely bipedal. Fossil evidence and cladistic analysis show that bipedality was the primitive dinosaurian condition -- the four-footed ones are more derived, in that respect, than two-footed dinosaurs. == Gould described interspecies transitionals within the snail genus _Cerion_ in Lake Turkana in Ethiopia. == Conway Morris's book on the Burgess Shale == This one shows a 250-fold change in an index of phenotype over a few generations, starting from a random sequence of DNA: Hayashi, Y., H. Sakata, Y. Makino, I. Urabe, and T. Yomo. 2003. Can an arbitrary sequence evolve towards acquiring a biological function. J. Mol. Evol. 56:162-168. Second, this one shows that a pathway of very small changes (each much, much less than 250-fold), each advantageous, by which a camera eye could develop from an eye spot: Nilsson, D., and S. Pelger. 1994. A pessimistic estimate of the time required for an eye to evolve. Proc. R. Soc. Lond. B 256:53-58. == The genus Spirochaeta includes 13 species of bacteria. Not all of them live in harsh places like Mono Lake. Some thrive in ordinary freshwater mud--the kind kids love to play in. Most, however, love extreme environments. Spirochaeta thermophila, for instance, can be found in the high-pressure mud around deep-sea hydrothermal vents. Another example: Spirochaeta bajacaliforniensis thrives without oxygen in the sulfurous muds of Baja California. All Spirochaeta are resistant to high sulfide concentrations. Hot, salty mud stinking of sulfur seems to be a good home for these creatures. == how mankind populated the world. The Journey of Man: A Genetic Odyssey by Spencer Wells == The first terrestrial vertebrates retained six to eight digits on each limb (more like a fish paddle than a hand), a persistent tailfin, and a lateral-line system for sensing sound vibrations underwater. The anatomical transition from reptiles to mammals is particularly well documented in the key anatomical change of jaw articulation to hearing bones. Only one bone, called the dentary, builds the mammalian jaw, while reptiles retain several small bones in the rear portion of the jaw. We can trace, through a lovely sequence of intermediates, the reduction of these small reptilian bones, and their eventual disappearance or exclusion from the jaw, including the remarkable passage of the reptilian articulation bones into the mammalian middle ear (where they became our malleus and incus, or hammer and anvil). We have even found the transitional form that creationists often proclaim inconceivable in theory for how can jawbones become ear bones if intermediaries must live with an unhinged jaw before the new joint forms? The transitional species maintains a double jaw joint, with both the old articulation of reptiles (quadrate to articular bones) and the new connection of mammals (squamosal to dentary) already in place! Thus, one joint could be lost, with passage of its bones into the ear, while the other articulation continued to guarantee a properly hinged jaw. == Consider the stability of the prion. An autoclave seems not to phase it. Nor does being baked at 600 degrees and buried for three years. It takes strong chemicals or extraordinary heat to "denature" this infectious, malformed protein. = The family-level classification of humans and apes is contraversial at present. The traditional classification system, based on morphological, ecological, and behavioural characteristics, segregates humans and apes into separate families (as in table 37.1). There is a close molecular relationship between humans and African apes, as noted in chapter 32. Some workers (Goodman and Moore 1971; Miamoto et al. 1988), using molecular evidence, propose a realignment in which humans and apes are placed in the same family (Hominidae); Humans and African apes are grouped in the same subfamily (Hominidae-Hominae); and the orangutan is separated into a separate family (Hominidae-Ponginae). --The Evolutionary Process, a critical study of evolutionary Theory 2nd Edition, (1991) by geneticist Verne Grant Even before this recent reclassification, human ancestry was traced from hominids were are classified as apes even according to Darwin. Apes [Homoidea] are essentially tailless versions of "Old-world" monkeys but with increased cranial capacity, an increased occipital arc in the shoulder and a and detition that includes cuspids, bicuspids and incisors, as well as canines and molars that come to five points interrupted by a Y-shaped crevasse. We all have opposable inner digits on at least two extremities, and none of us can naturally produce vitamin-C. === There are many mysteries of life but to say our love of music proves Darwin wrong would be to deny the evidence that art itself has evolved from very primitive paintings to works such as the Mona Lisa or from beating on a hollow log to Beethoven's Ninth Symphony. Our creativity was expressed right along with our evolving brain, first tools would be carved but before long many of the tools took on a new life as decorations and eventually fully formed statues of make believe gods and mankind. == All the DNA does is provide a template for the primary RNA or DNA sequence of the product, but that's mostly enough. For example, DNA *does* provide the information for alternative splicing, in the sense that it encodes the RNA and protein components of the spliceosome and the template for the RNA sequence at the alternative splice site itself. The primary amino acid sequence (which, of course is derived from the DNA sequence) of a protein often is adequate to determine its final conformation and, for enzymes, enzymatic activity, e.g. ribonuclease, for a really robust example of that. But even in cases where you need a chaperonin to assist in folding, that chaperonin's conformation and activity are determined by its own primary sequence, the information for which comes from DNA. Even if the protein needs to be glycosylated to be active, the enzymes that attach the sugars are targetted to the Golgi based on a tag sequence that ultimately comes from the DNA sequence of the gene encoding them, and their enzymatic activity depends on their higher-order structure, which depends on their primary sequence, which is encoded in the DNA. DNA certainly does control how proteases clip other proteins, simply by determining the primary structure of both the protease and its protein substrate - you can get proper proteolytic cleavage of HIV proteins following in vitro transcription and translation from a DNA version of the HIV geneome. DNA certainly controls the presence of DNA binding proteins - it encodes them, it contains cis-acting elements that regulate their expression and it encodes the trans-acting elements that bind the cis acting elements. == Noah's story has recently been disproved with genetic evidence showing that we could not have all descended from a middle eastern man four thousand years ago. We have however descended from someone in Africa around 60 thousand years ago. ****************************************************************************** ** End of Bible B12A-Evolve-A1.txt ========== B13A-Evolve-A2.txt ******************************************************************************* Graham L. Kendall Modified 8/3/2005 Email grahamkendall74135@yahoo.com I am found on IRC Efnet, Undernet, Dalnet as glk Files found at http:www.grahamkendall.net/ All are free to use any of this material without limit. ============= Around a million years ago, an ape so large that it's now known as Gigantopithecus roamed the bamboo forests of South Asia. Standing nine feet tall, weighing from 600 to 1,000 pounds, and with a bamboo-crushing jaw the size of a mailbox, this was a truly strong creature. But today, all that remains of Gigantopithecus are a few fossil teeth and jawbones in museum vaults. == Many people confuse evolutionary theory with Lamarckism, named for the French naturalist Jean-Baptiste Lamarck (1744-1829). In one sense Lamarck was an evolutionist in that he favored the view that new species had evolved from ancestral species, but he was mistaken about the mechanism by which species change, and about the time required for these changes. Lamarck thought that the mechanism for biological change was the transmission to the next generation of characteristics acquired during the life span of an individual. His most famous example is that of the giraffe. According to Lamarck, the giraffe's ancestors had shorter necks, and they would stretch their necks to reach higher foliage in trees. Their descendants then inherited longer necks because the characteristics of these newly stretched necks of the parents were passed down to their offspring. Moreover, Lamarck thought that the evolution of a new species could occur within a few generations or even one. His position was reasonable for its time, yet it happens to be incorrect. == Over the past 40 million years, more than 600 species of elephants have roamed the earth. Today only three species remainthe savanna elephant and the forest elephant of Africa, and the Asian elephant. There are two genera of extant elephants: Elaphus and Loxodonta. list of the extinct genera: http://www.elephant.se/proboscidea.php == The 100% match of DNA sequences in the pseudogene region of beta-globin was proof that humans and gorillas shared a recent common ancestor. == Mitochondria are the main sites of biological energy generation in eukaryotes. These organelles are remnants of a bacterial endosymbiont that took up residence inside a host cell over 1,500 million years ago. Comparative genomics studies suggest that the mitochondrion is monophyletic in origin. Thus, the original mitochondrial endosymbiont has evolved independently in anaerobic and aerobic environments that are inhabited by diverse eukaryotic lineages. This process has resulted in a collection of morphologically, genetically and functionally heterogeneous organelle variants that include anaerobic and aerobic mitochondria, hydrogenosomes and mitosomes. Current studies aim to determine whether a central common function drives the retention of mitochondrial organelles in different eukaryotic organisms. == Science (published by the American Association for the Advancement of Science) http://www.sciencemag.org/ Nature http://www.nature.com/ Journal of Biology (published by BioMed Central) http://jbiol.com/ Journal of Evolutionary Biology http://www.blackwellpublishing.com/journal.asp?ref=1010-061X view online content: http://www.blackwell-synergy.com/rd.asp?code=JEB&goto=journal International Journal of Organic Evolution http://evol.allenpress.com/evolonline/ ?request=index-html#Evolution_Journal [link is line-wrapped] Molecular Biology and Evolution (published by the Society for Molecular Biology and Evolution) http://www.mbe.oupjournals.org Evolution & Development http://www.blackwellpublishing.com/journal.asp?ref=1520-541X Trends in Ecology & Evolution http://www.elsevier.com/wps/find/journaldescription.cws_home/ 30339/description [link is line-wrapped] Integrative and Comparative Biology (Journal of the Society for Integrative and Comparative Biology; published as the American Zoologist from 1961 to 2001) http://www.sicb.org/az/ Invertebrate Biology (Journal of the American Microscopical Society) http://www.invertebratebiology.org/ Proceedings of the National Academy of Sciences (PNAS) Biological Sciences http://www.pnas.org/current.shtml#BIOLOGICAL_SCIENCES Palobiology Journal of Paleontology (both published by The Paleontological Society) http://www.psjournals.org/paleoonline/?request=get-archive The Journal of Vertebrate Paleontology (published by the Society of Vertebrate Paleontology) http://www.vertpaleo.org/jvp/ Paleontologia Electronica http://palaeo-electronica.org/ == 1. Did we evolve from monkeys? Humans did not evolve from monkeys. Humans are more closely related to modern apes than to monkeys, but we didn't evolve from apes, either. Humans share a common ancestor with modern African apes, like gorillas and chimpanzees. Scientists believe this common ancestor existed 5 to 8 million years ago. Shortly thereafter, the species diverged into two separate lineages. One of these lineages ultimately evolved into gorillas and chimps, and the other evolved into early human ancestors called hominids. http://www.primates.com/pierolapithecus/ Scientists in Spain have discovered fossils of an ape species from about 13 million years ago that they think may have been the last common ancestor of all living great apes, including humans. The new ape species and its possible place in prehuman evolution are described in today's issue of the journal Science by a research team led by Dr. Salvador Moya-Sola of the Miquel Crusafont Institute of Paleontology in Barcelona. The fossil remains were found near Barcelona and named Pierolapithecus catalaunicus. About 25 million years ago, Old World monkeys diverged from the primate line that led eventually to apes and humans. About 11 million to 16 million years ago, another branching occurred, when primates known as the great apes - which now include orangutans, chimpanzees, gorillas and humans - split from the lesser apes, represented by today's gibbons and siamangs. The lineage leading to humans branched off from the chimpanzee line an estimated seven million years ago. == Stress and Mutations A few years ago, when he was first starting to think about this, Romesberg encountered a paper in a scientific journal that discussed certain genes that "make mutations," as he put it. When these genes are deleted from cells, the cells lose their ability to mutate, even when subjected to massive amounts of ultraviolet light. This brought Romesberg to the conclusion that mutation is a programmed stress response a survival mechanism. If the cell senses damage, and if the damage persists beyond its ability to repair it, the cell will turn on its mutation machinery and open the floodgates for evolution" 2. Rate new allele reaches fixation (or at least becomes established in the population). Other mechanisms affecting the fixation of new mutations include drift, nonrandom mating, and migration (gene flow). If they controlled for nonrandom mating and eliminated migration, then drift has a larger role. There is a nice population genetics package - Populus http://www.cbs.umn.edu/populus/ down load and play with the mendelian genetics programs. They're easy to run and you can test the drift hypothesis your self. == Although many have heard that being heterozygous for sickle cell anemia (having one copy each of the good and bad alleles) is beneficial in some areas of Africa due to the protective benefit it provides against malaria, many do not know that this relationship also seems to be prevalent in the US concerning cystic fibrosis (CF) and secretory diarrheas. In CF, a chloride channel in the lungs does not function properly and so less chloride is allowed to flow into the airways of the lung. With less chloride there is less water that follows, and with less water you get more mucous which leads to a variety of problems for the lungs. This is not generally a problem for those who are only carriers (i.e. heterozygous) of CF, however, and in fact in some circumstances it may provide a direct benefit in other parts of the body. Aside from the lungs, other organs use the same chloride channel are still moderately impeded even if the person is only a carrier for a defective channel. Interestingly, this is exactly the case with intestine which, like the lungs, uses the channel to help secrete water into the intestinal lumen. Normally this is not significant enough of a problem to affect the individual much, but it does become relevant with secretory diarrheas. In cholera, one form of secretory diarrhea, a toxin produced by the bacterium leads to the constant efflux of chloride through the channel no matter what the body wants it to do, and so along with the chloride goes a large volume of water. This loss of fluid is so severe that it is actually the greatest cause of death from cholera. People with one copy of a defective chloride channel, however, are unable to lose as much chloride as a result of the toxin and so experience much water loss and much less mortality as a result of the disease. This has perhaps, it is theorized, led to CF being the most prevalent autosomal recessive disorder in the United States with 1 in 20 adults being carriers. == vestigial organs The eyes of cave fish? The eyes of cave salamanders? The pelvises inside the skin of pythons? The legs inside some other lizards that never get outside of the skin? The perfectly formed wings housed underneath fused wing covers within flightless beetles (such as the weevils of the genus Lucanidae)? The third molars (otherwise known as wisdom teeth) which develop in over 90% of all adult humans yet never erupt from the gums, and in one third of all individuals they are malformed and impacted? == "Sex" [a life cycle with syngamy & meiosis] first arose in unicellular organisms, since many unicellular eukaryotes still show it today. The first multicellular organisms thus would already have been sexually reproductive at the outset; there would have been some sort of gamete-forming areas in even the earliest animals with differentiated tissues. Some living types of algae and fungi do illustrate intermediate stages in the evolution of differentiated sperms and eggs [oogamy] from undifferentiated gametes [isogamy] == The theory of evolution describes the mechanisms that cause evolution. So evolution is both a fact and a theory. See the Evolution is a Fact and a Theory FAQ, the http://www.talkorigins.org/faqs/evolution-fact.html Introduction to Evolutionary Biology FAQ and the Five Major http://www.talkorigins.org/faqs/faq-intro-to-biology.html Misconceptions about Evolution FAQ. http://www.talkorigins.org/faqs/faq-misconceptions.html#proof COMPARATIVE GENETICS: Which of Our Genes Make Us Human? Ann Gibbons Science 1998 September 4; 281: 1432-1434. (in News Focus) HUMAN EVOLUTION: Y Chromosome Shows That Adam Was an African Ann Gibbons Science 1997 October 31; 278: 804-805. (in Research News) Miocene Primates Go Ape Ann Gibbons and Elizabeth Culotta Science 1997 April 18; 276: 355b-356b. (in Research News) A Hominoid Genus from the Early Miocene of Uganda Daniel L. Gebo, Laura MacLatchy, Robert Kityo, Alan Deino, John Kingston, and David Pilbeam Science 1997 April 18; 276: 401-404. (in Reports) Human or Chimp? 50 Genes Are the Key http://www.nytimes.com/library/national/science/102098sci-chimps.html http://www.bbc.co.uk/horizon/hopefulmonsters.shtml http://inia.cls.org/~welsberr/evobio/evc/argresp/sequence.html http://lummi.stanford.edu/class/anthro276/WWW/EvAnth.html Talk Origins Archive FAQ http://www.talkorigins.org/origins/faqs-qa.html Suspicious Creationist Credentials FAQ http://www.talkorigins.org/faqs/credentials.html Talk.Origins Archive's Creationism FAQs http://www.talkorigins.org/origins/faqs-creationists.html Many people of Christian and other faiths accept evolution as the scientific explanation for biodiversity. See the God and http://www.talkorigins.org/faqs/faq-god.html Evolution FAQ and the Interpretations of Genesis FAQ. http://www.talkorigins.org/faqs/interpretations.html == 1] the support for the concept of evolutionary common descent isn't so much from paleontology as from all of comparative biology. 2] It isn't just that the transitionals \look similar to [whatever] but have some differences\, but instead it requires more careful comparisons and analyses of the detailed patterns of similarities and differences among the fossils and their putative relatives. Shared similarities among species that are due to common descent will show a hierarchically nested pattern of groups within groups within groups. [You might look up phylogenetic systematics or cladistics for more info on the types of analytical methods used: http://www.ucmp.berkeley.edu/clad/clad4.html The finders of fossils of an new type of early australopithecine might say something more like here is a very early hominid fossil that is in-betweenhumans and apes in these specific ways. This pattern of shared features is very consistent with it being an early species of the human group, at some point after the origin of the group from the last common ancestor of modern chimps and modern humans.\ fossil...or, Enough to document lots of interesting evolutionary transitions: The nested hierarchical pattern was recognized long before the concept of evolution provided the explanation for its existence. The fact that independent data sets like DNA and morphology tend to give highly compatible results [the twin nested hierarchies] is even more compelling evidence. http://www.talkorigins.org/origins/faqs-evolution.html http://www.talkorigins.org/faqs/faq-transitional.html http://www.talkorigins.org/faqs/fossil-hominids.html http://www.talkorigins.org/faqs/archaeopteryx.html http://www.dinosauria.com/jdp/jdp.htm http://www.talkorigins.org/faqs/horses.html http://www.neoucom.edu/Depts/Anat/Whale.html Zimmer, Carl. 1998. At the water's edge: macroevolution and the transformation of life. New York : Free Press. Padian, K. & L. M. Chiappe. 1998. The origin of birds and their flight. Scientific American 278[2]: 38-47 [Feb. 1998]. Padian, K. & L. M. Chiappe. 1998. The origin and early evolution of birds. Biological Reviews 73: 1-42. == Most paleontologists have agreed based on a variety of empirical evidence that birds are the direct descendants of a particular group of dinosaurs, but a consistent minority of scientists has disagreed (which, contrary to claims by supporters of pseudo-science, isn't a sign of crisis at all, but rather of a healthy critical debate among scientists). One of the "bones" of contention, so to speak, was represented by the development of fingers in birds and dinosaurs: both kinds of animals have three fingers as adults, as opposed to the five that are normal for vertebrates in general. Until now, however, scientists thought that while dinosaurs retained digits n. 1, 2 and 3, birds had lost n. 1 and retained the three middle digits. This would count as evidence against a close phylogenetic connection between the two groups. But new molecular developmental work has actually shown that what looks superficially like digit n. 2 in birds is really the standard first digit of vertebrates in general. Molecular biologists have been able to determine this by examining which genes are involved in the formation of the various digits in the developing bird embryo. Therefore, what seemed until recently an out of place piece of the puzzle turns out to fit perfectly with the prevailing hypothesis. This is the way science works: if new evidence supports the accepted hypothesis, the latter receives further confirmation and grows in strength and acceptance; if enough new pieces of evidence don't fit, eventually the hypothesis is discarded in favor of an alternative that explains things better. == A.G. Cairns-Smith, 1986 Andrew Scott, 1999 Freeman Dyson Timeline of Materialism, Spontaneous Generation, and Blindwatchmaking Views == here on Earth. 90 percent of terrestrial soil bacteria cannot be grown in culture. == "The analysis revealed clear evidence that photosynthesis did not evolve through a linear path of steady change and growing complexity but through a merging of evolutionary lines that brought together independently evolving chemical systems -- the swapping of blocks of genetic material among bacterial species known as horizontal gene transfer." == POITIERS, FRANCE-Michel Brunet removes the cracked, brown skull from its padlocked, foam-lined metal carrying case and carefully places it on the desk in front of me. It is about the size of a coconut, with a slight snout and a thick brow visoring its stony sockets. To my inexpert eye, the face is at once foreign and inscrutably familiar. To Brunet, a paleontologist at the University of Poitiers, it is the visage of the lost relative he has sought for 26 years. "He is the oldest one," the veteran fossil hunter murmurs, "the oldest hominid." Brunet and his team set the field of paleoanthropology abuzz when they unveiled their find last July. Unearthed from sandstorm-scoured deposits in northern Chad's Djurab Desert, the astonishingly complete cranium-dubbed Sahelanthropus tchadensis (and nicknamed Toumai, which means "hope of life" in the local Goran language)-dates to nearly seven million years ago. It may thus represent the earliest human forebear on record, one who Brunet says "could touch with his finger" the point at which our lineage and the one leading to our closest living relative, the chimpanzee, diverged. == Pachycynodon -- A bearlike terrestrial carnivore with several sea-lion traits. == Piltdown was an indisputable fraud. No one knows for sure who perpetrated it. It was fairly sophisticated so it is likely that someone with a scientific background was involved. The most interesting name among the suspects is Sir Arthur Conan Doyle. Piltdown fooled scientists for about 40 years (though beginning in 1925, some scientists found discrepancies that they couldn't explain and after 1930 or so most discussions of hominid evolution didn't mention Piltdown). In 1953 it was formally denounced as a fraud by evolutionary scientists. The primary evidence was the inconsistent way that the teeth were worn down. The reasons that the fraud took so long to expose were the relatively weak tools available to the people who found Piltdown: chemical tests and dating techniques taken for granted today were not available; the analysis of the details of tooth wear was less worked out; the simple knowledge of geology was much less detailed. Of course the people who found Piltdown may have been the perpetrators of the fraud as well. == Residual amino acids have been found in fossil shells of mollusks up to 80 million years old. == Patterson, In several animal and plant groups, enough fossils are known to bridge the wide gaps between existing types. In mammals, for example, the gap between horses, asses and zebras (genus Equus) and their closest living relatives, the rhinoceroses and tapirs, is filled by an extensive series of fossils extending back sixty-million years to a small animal, Hyracotherium, which can only be distinguished from the rhinoceros-tapir group by one or two horse-like details of the skull. There are many other examples of fossil 'missing links', such as Archaeopteryx, the Jurassic bird which links birds with dinosaurs (Fig. 45), and Ichthyostega, the late Devonian amphibian which links land vertebrates and the extinct choanate (having internal nostrils) fishes. . . [from Lionel Theunissen's page at http://www.talkorigins.org/faqs/patterson.html] "When quoting scientists like Patterson or Gould as saying 'there are no transitional forms' they neglect to mention that they are only referring to transitional forms at the species level. They know full well that Gould has stated that transitional forms between orders and families are in fact abundant, and even a cursory read of Dr. Patterson's book will yield numerous examples of transitional forms." The overall point is that, even if we cannot prove that any *individual* fossil or species is a transitional, we *can* prove that *most* of the ones we suppose to be transitionals really are transitionals or very closely related to organisms that *were* transitionals. We can do this because the pattern is one that forces the conclusion that transitionals existed and that the species were *not* all separately created (but merely on common patterns in many cases). Evolution says that species arise over time and gradually (i.e., not in single huge leaps from one species to another overnight), even in punctuated equilibrium theories. Evolution says because the mechanism that it uses for explaining things is an *incremental* mechanism, involving single steps that are always relatively small, because new traits must start out in such a way as not to disrupt the entire organism (one reason the Cambrian explosion was possible was that, at that time, the existing species were simple enough that fairly major changes could occur relatively rapidly, with a short reproductive cycle and with major changes in body form not requiring major *physiological* changes as well -- increasing complexity of integration of many distinct parts in a rigid format has caused a great slowdown because of the necessity that all new parts be added in such a way as to integrate with *many* existing parts, not just a few). In the case of evolution, we have a *process* that either leads to adaptation or extinction, and which explains adaptation in terms of the three factors of replication, modifications that may themselves be passed on, and natural selection to determine *which* modifications *do* get passed on. For any sufficiently slowly-changing environment, this process will produce progressive adaptations in at least *some* species so as to "track" the changes in the environment (actually, this tracking is not perfect, and may often lag somewhat behind) There are many cases where a morphologically intermediate form is also *well* established as a *transitional* form as well. These would be cases where the fossil record is fairly complete, showing a good grouping of species over levels such that we can be pretty sure that no *other* species could be the transitional than the one candidate for a particular "slot" in the sequence. == Evolutionary change is observed in the field occuring at rates far too fast to allow for a complete fossil record. The fossil record is spotty for well known reasons. The pattern in the fossil record is entirely consistent with Darwinian evolution (and Punctuation is simply a call for plurality: *some* evolution happens in small populations in geographically restricted ranges and at relatively high rates, none of which is a violation of Darwinism). Evolution by natural selection is, therefore, the *best available* explanation. It should be abandoned or reconsidered if contradicted by the evidence or when a competing theory of comparible explanitory power is introduced. It should not be abandoned based on an inability to find evidence in quantities or qualities which would be nice to have, but we have no reason to expect exist. Life can be arranged, with some effort, into a clearly nested heirarchy. This pattern is predicted by common descent with modification, and not predicted by design or design economy arguments for similarity. Similarities as a result of heredity are a well-observed phenomena and it can quite reasonably be argued that morphological similarity, of a certain kind and quality, is evidence of a hereditary connection. Similarity implies common descent is not a 'bare' assumption, it is based on fundamental observations. === [Q.] I thought evolution was just a theory. Why do you call it a fact? [A.] The phenomena of biological evolution are changes in the heritable characteristics of populations over time. That these occur is a fact. Biological evolution refers to the common descent of all living organisms from shared ancestors. The evidence for this historical evolution -- genetic, fossil, anatomical, etc. -- is so overwhelming that it is also considered a fact. The theory of evolution describes the mechanisms that cause evolution. So evolution refers to both fact and theory. [U.] http://www.talkorigins.org/faqs/evolution-fact.html http://www.talkorigins.org/faqs/faq-intro-to-biology.html http://www.talkorigins.org/faqs/faq-misconceptions.html#proof [Q.] Don't you have to be an atheist to accept evolution? [A.] No. Many people of Christian and other faiths accept evolution as the scientific explanation for biodiversity. [U.] http://www.talkorigins.org/faqs/faq-god.html http://www.talkorigins.org/faqs/interpretations.html [Q.] Isn't evolution just an unfalsifiable tautology? [A.] No. Evolutionary theory is in exactly the same condition as any other valid scientific theory, and many criticisms of it that rely on philosophy are misguided. [U.] http://www.talkorigins.org/faqs/evolphil.html [Q.] If evolution is true, then why are there so many gaps in the fossil record? Shouldn't there be more transitional fossils? [A.] Due to the rarity of preservation and the likelihood that speciation occurs in small populations during geologically short periods of time, transitions between species are uncommon in the fossil record. Transitions at higher taxonomic levels, however, are abundant. [U.] http://www.talkorigins.org/faqs/faq-transitional.html http://www.talkorigins.org/faqs/fossil-hominids.html http://www.talkorigins.org/faqs/punc-eq.html http://www.talkorigins.org/origins/postmonth/feb98.html [Q.] No one has ever directly observed evolution happening, so how do you know it's true? [A.] Evolution has been observed, both directly and indirectly. It is true. [U.] http://www.talkorigins.org/faqs/faq-misconceptions.html#observe http://www.talkorigins.org/faqs/comdesc/ [Q.] Then why has no one ever seen a new species appear? [A.] Speciation has been observed both in the laboratory and in nature. [U.] http://www.talkorigins.org/faqs/faq-speciation.html http://www.talkorigins.org/faqs/speciation.html [Q.] Doesn't the perfection of the human body prove Creation? [A.] No. In fact, humans (and other animals) have many suboptimal characteristics. [U.] http://www.talkorigins.org/faqs/jury-rigged.html [Q.] According to evolution, the diversity of life is a result of chance occurrence. Doesn't that make evolution wildly improbable? [A.] Evolution is not simply a result of random chance. It is also a result of non-random selection. [U.] http://www.talkorigins.org/faqs/chance.html http://www.talkorigins.org/faqs/faq-misconceptions.html#chance [Q.] Doesn't evolution violate the second law of thermodynamics? After all, order cannot come from disorder. [A.] Evolution does not violate the second law of thermodynamics. Order emerges from disorder all the time. Snowflakes form, trees grow, and embryos develop, etc. [U.] http://www.talkorigins.org/faqs/thermo.html http://www.talkorigins.org/faqs/faq-misconceptions.html#thermo [Q.] Didn't Darwin renounce evolution on his deathbed? [A.] The Darwin deathbed story is false. And in any case, it is irrelevant. A scientific theory stands or falls according to how well it is supported by the facts, not according to who believes it. [U.] http://www.talkorigins.org/faqs/hope.html [Q.] Where can I learn more about evolution? [A.] You might start with the talk.origins FAQs. If, however, you want a deeper understanding of evolution, a library would be a more appropriate place to look. The FAQs listed below provide some good references. [U.] http://www.talkorigins.org/faqs/reading-list.html http://www.talkorigins.org/faqs/faq-intro-to-biology.html http://www.talkorigins.org/faqs/evolution-definition.html [Q.] How do you know the earth is really old? Lots of evidence says it's young. [A.] According to numerous, independent dating methods, the earth is known to be approximately 4.5 billion years old. Most young-earth arguments rely on inappropriate extrapolations from a few carefully selected and often erroneous data points. [U.] http://www.talkorigins.org/faqs/faq-age-of-earth.html http://www.talkorigins.org/origins/faqs-youngearth.html [Q.] But radiometric dating methods rely on the assumptions of non- contamination and constant rates of decay. What if these assumptions are wrong? [A.] Isochron dating techniques reveal whether contamination has occurred, while numerous theoretical calculations, experiments, and astronomical observations support the notion that decay rates are constant. [U.] http://www.talkorigins.org/faqs/isochron-dating.html http://www.talkorigins.org/faqs/faq-age-of-earth.html [Q.] I heard that the speed of light has changed a lot. This means that light from galaxies billions of light years away might not be billions of years old. Is this true? [A.] Barry Setterfield's hypothesis of a decaying speed of light was based on flawed extrapolations from inaccurate measurements, many of which were taken hundreds of years ago. [U.] http://www.talkorigins.org/faqs/c-decay.html [Q.] If the Earth is so old, doesn't that mean the Earth's decaying magnetic field would have been unacceptably high at one time? [A.] No. The Earth's magnetic field is known to have varied in intensity and reversed in polarity numerous times throughout the planet's history. [U.] http://www.talkorigins.org/faqs/magfields.html [Q.] Isn't the fossil record a result of the global flood described in the Book of Genesis? [A.] No. A global flood cannot explain the sorting of fossils observed in the geological record. This was recognized even prior to the proposal of evolutionary theory. [U.] http://www.talkorigins.org/faqs/faq-noahs-ark.html http://www.talkorigins.org/origins/postmonth/apr02.html [Q.] What about those fossils that cut through multiple layers? [A.] They have natural explanations: tree-roots that grew into soft, underlying layers of clay, and fossils found in inclined strata. They can also be observed forming in modern environments. [U.] http://www.talkorigins.org/faqs/polystrate.html [Q.] What about those human footprints that appear next to dinosaur footprints? [A.] The "man-tracks" of the Paluxy Riverbed in Glen Rose, Texas were not man tracks at all. Some were eroded dinosaur tracks, and others were human carvings. [U.] http://www.talkorigins.org/faqs/paluxy.html [Q.] Didn't they find Noah's Ark? I saw something on TV about this. [A.] The producers of America's 1993 CBS television show, "The Incredible Discovery of Noah's Ark," were hoaxed. Other ark discovery claims have not been substantiated. [U.] http://www.talkorigins.org/faqs/ark-hoax.html [Q.] The odds against a simple cell coming into being without divine intervention are staggering. [A.] And irrelevant. Scientists don't claim that modern cells came into being through random processes. They are thought to have evolved from more primitive precursors. [U.] http://www.talkorigins.org/faqs/abioprob/ [Q.] Creationists are qualified and honest scientists. How can they be wrong? [A.] The quality of an argument is not determined by the credentials of its author. Even if it was, a number of well-known creationists have questionable credentials. Furthermore, many creationists have engaged in dishonest tactics like quoting out of context or making up references. [U.] http://www.talkorigins.org/faqs/credentials.html http://www.talkorigins.org/origins/faqs-creationists.html http://www.talkorigins.org/faqs/quotes/ http://www.talkorigins.org/faqs/homs/misquotes.html [Q.] What about Immanuel Velikovsky? Didn't he show that the Earth has experienced a lot of major catastrophes? [A.] No, he simply claimed that certain written legends must have described real events. [U.] http://www.talkorigins.org/origins/faqs-catastrophism.html http://www.talkorigins.org/faqs/faq-velikovsky.html [Q.] Where can I find more material on the Creation/Evolution debate? [A.] Contact the National Center for Science Education, or see the TalkOrigins Archive and its \Other links\ page. [U.] http://www.NatCenSciEd.org/ http://www.talkorigins.org/faqs/reading-list.html http://www.talkorigins.org/faqs/organizations.html http://www.talkorigins.org/origins/other-links.html [Q.] What about \intelligent design\? [A.] \Intelligent design\ advocates often use the very same arguments that the young-earth creationists have used in the past. The Archive does have some FAQs on Behe's \irreducible complexity\, Jonathan Wells's \icons of evolution\, and Dembski's \specified complexity\ (see questions below). Further essays on \intelligent design\ can be found on our sister site, TalkDesign, and also at the TalkReason site. [U.] http://www.talkdesign.org http://www.talkreason.org http://www.talkdesign.org/faqs/hunch/hunch.html [Q.] Doesn't irreducible complexity (as described in Behe's _Darwin's Black Box_) shown that some biomechanical systems could not evolve gradually, but must have all their parts created at once? [A.] Behe's \irreducible complexity\ considers only an unrealistically simplistic model of evolution. Evolutionary mechanisms that Behe doesn't consider, such as functional change and coevolution, make irreducible complexity not only possible, but expected. [U.] http://www.talkorigins.org/faqs/behe.html http://www.talkdesign.org/faqs/icdmyst/ICDmyst.html [Q.] Hasn't Jonathan Wells shown that Darwinist claims about such "icons of evolution" as the peppered moth, Haeckel's embryos, and Darwin's finches have been disproven? If so, why are these claims still found in biology textbooks? [A.] Scientists _have_ been complaining for decades about the poor quality of science instruction in school and about the content of science textbooks. However, Dr. Wells's arguments include many false statements, many misunderstandings of the science involved, and many misunderstandings of the significance of the subjects that he pontificates on. [U.] http://www.talkorigins.org/faqs/wells/ http://www.ncseweb.org/pdf/QRBreview.pdf [Q.] Doesn't William Dembski's \specified complexity\ mean that an intelligent designer had to be responsible for the observed complexity and diversity of living things? [A.] The sophistication of Dembski's arguments is superficial. One of the most thorough examinations of Dembski's ideas is available on the Archive. [U.] http://www.talkorigins.org/design/faqs/nfl/ http://www.talkdesign.org/faqs/present_arguments.html http://www.talkdesign.org/faqs/demskiscompass.html http://www.antievolution.org/people/dembski_wa/ [Q.] Isn't it true that scientists are abandoning evolution? [A.] That is not even remotely true. [U.] http://home.entouch.net/dmd/moreandmore.htm [offsite] http://www.talkorigins.org/faqs/steve/ http://www.talkorigins.org/faqs/edwards-v-aguillard/amicus1.html [Q.] If evolution is true, why don't you take Dr. Kent Hovind's $250,000 challenge and make yourself rich? [A.] Kent Hovind's $250,000 challenge is a propaganda ploy and nothing more, rather like the \doctorate\ Hovind claims from Patriot University. [U.] http://www.talkorigins.org/faqs/hovind/ [Q.] Don't you know that the earth is round? [A.] Yes, we do. We keep a copy of the "International Flat Earth Society" flyer here to document that real people in modern times do assert that the earth is flat, not because *we* think the earth is flat. [U.] http://www.talkorigins.org/faqs/flatearth.html == Sex [a life cycle with syngamy & meiosis] first arose in unicellular organisms, since many unicellular eukaryotes still show it today. The first multicellular organisms thus would already have been sexually reproductive at the outset; there would have been some sort of gamete-forming areas in even the earliest animals with differentiated tissues. Some living types of algae and fungi do illustrate intermediate stages in the evolution of differentiated sperms and eggs [oogamy] from undifferentiated gametes [isogamy] == The only organism which uses RNA exclusively are retroviruses. The only difference between ribose and deoxyribose is the reduction of a hydroxyl group on the ribose #2 carbon. Biochemically, this reduction is catalyzed by a single enzyme. In addition, ribonucleic acids use the base uracil, in place of the base thymidine which is found in deoxyribonucleic acids. The difference here is a single methyl group, which isn't even involved in hydrogen bonding with opposite bases in the spiral.. == Recent reviews of the available anatomical (Shoshani et al. 1996) and genetic evidence (Ruvolo 1995, 1997; Wise et al. 1997) have convincingly re-affirmed yet again the theory that apes and anatomically modern humans share a common ancestry. Geneticists have analysed the differences in the amino acid sequences of protein and in the base sequences of DNA from apes and humans. The results have yielded a divergence time-frame of 5-8 million years ago. The anatomical differences and similarities can be summarised as follows: - Apes have larger and more sexually dimorphic canines. The spacing layout is also different. - Human jaws are less robust and forward projecting. - The foramen magnum is more centrally orientated at the skull base in modern humans than in apes. - Humans have a larger brain capacity with regards to endocranial volume:body mass - The human cranial base is wider and shorter. Apes and humans share a transversely broad thoracic cage, a vertebral column inside the rib cage, a dorsally-placed scapula and laterally-facing shoulder joints. - The human thorax is relatively uniform in width, whereas the ape thorax widens towards the base. These differences are due to their different gut shapes. - Upper human limbs are less robust because they no longer server as weight-bearers. A side-effect is that they now have a greater ability for motion. - The human mobile shoulder joint is an indicator of our arboreal ancestry and has undergone only comparatively minor alterations. - Human limbs are shorter in proportion to body size than in apes. However, this discrepancy occurs in the length of our lower limbs. - "In African apes and humans, the humeral shaft twists from the humeral head, which faces medially, down to the coronally oriented elbow joint." (Wood & Richmond 2000: 12) - The human and ape elbow structures have very few distinctions. - The human wrist has more dexterity, for greater tool manipulation. This is closely linked to the precision grip, the first hominin occurrences of which are in Homo habilis and some of the australopiths. - Apes have longer and more curved phalanges, which are related to their greater arboreal lifestyle. Australopiths display intermediary lengths. - Lower limb morphology differs to a larger degree than upper limb morphology between humans and apes: "The substantial differences between the lower limbs of modern humans and apes are largely attributable to the bipedal locomotion of the former. The most striking difference is the greater absolute and relative length of modern human lower limbs that > increases stride length and thus the speed of bipedal walking (Jungers 1982). Because the lower limbs support the body during bipedal gait, the acetabulum, femoral head and other lower limb joints are relatively larger in humans (Jungers 1988). Modern human femora are distinctive in that they show the valgus condition (i.e. they converge towards the knee), thus helping to position the feet closer to the midline (Walmsley 1933; Tardieu & Trinkaus 1994)." (Wood & Richmond 2000) - Bipedalism is evident right back with Ardipthecus ramidus at least 4.4 million years ago. The Laetoli footprints were made by a hominin with a divergent big toe and are attributable to Australopithecus afarensis, whose remains have been found in the same stratigraphic layers in the same time-frame at Laetoli. Wood & Richmond (2000: 23) state it clearly when they say that "the presumption is that the common ancestor and the members of the Pan lineage would have had a locomotor system that is adapted for orthograde arboreality and climbing, and probably knuckle-walking as well (Washburn 1967; Pilbeam 1996; Richmond & Strait 1999). This would have been combined with projecting faces accomodating elongated jaws bearing relatively small chewing teeth, and large, sexually-dimorphic, canine teeth with a honing system. Early hominins, on the other hand, would have been distinguished by at least some skeletal and other adaptations for a locomotor strategy and other adaptations for a locomotor strategy that includes substantial bouts of bipedalism (Rose 1991), linked with a masticatory apparatus that combines relatively larger chewing teeth, and more modest-sized canines that do not project as far above the occlusal plane." References Jungers, W.L. 1988. Relative joint size and hominoid locomotor adaptations with implications for the evolution of hominid bipedalism. In, Strasser, E. & Dagosto, M. (eds.) The Primate Postcranial skeleton: Studies in Adaptation and Evolution, pp. 247-265. London: Academic Press Pilbeam, D. 1996. Genetic and morphological records of the Hominoidea and hominid origins: a synthesis. Molecular Phylogenetics and Evolution 5: 155-168 Richmond, B. & Strait, D. 1999. Knuckle-walking traits retained in the wrists of early hominids. American Journal of Physical Anthropology, Suppl. 28: 232 Shoshani, J. et al. 1996. Primate phylogeny: morphological vs molecular results. Molecular Phylogenetic Evolution 5: 101-153 Tardieu, C. & Trinkaus, E. 1994. Early ontogeny of the human femoral bicondylar angle. American Journal of Physical Anthropology 95: 183-195 Walmsley, T. 1933. The vertical axes of the femur and their relations. A contribution to the study of erect posture. Journal of Anatomy 67: 284-300 Washburn, S.L. 1967. Behaviour and the origin of Man. Proceedings of the Royal Anthropological Institute 3: 21-27 Wise, C. et al. 1997. Comparative Nuclear and Mitochrondrial Genome Diversity in Humans and Chimpanzees. Molecular Biology Evolution 14 (7): 707-716 Wood, B. & Richmond, B. 2000. Human evolution: taxonomy and paleobiology. Journal of Anatomy 196: 19-60 Douglas J. Futuyma, Evolutionary Biology, 2nd ed., 1986, Sinauer Associates == Before 2.4 billion to 2.2 billion years ago, the Earth's atmosphere contained almost no oxygen and could support only single-celled forms of life. The first complicated cells, like the ones that make up today's plants and animals, appear in 2.1 billion-year-old fossils just after the rise of oxygen. theory of high levels of hydrogen-containing methane gas, which acquired its hydrogen indirectly from water, also would account for why early Earth didn't freeze. "Three billion years ago, the sun was only 4/5ths as bright as it is now. The Earth should have frozen over," he said. But methane, a powerful greenhouse gas, would have kept the Earth warm. == In human DNA, the 21-hydroxylase gene sequence, as well as an adjacent gene encoding complement C4, has been duplicated; i.e., nearly identical copies of DNA segments lie adjacent to each other, each copy containing a complement C4 gene and a steroid 21-hydroxylase sequence. However, only the B copy of the 21-hydroxylase gene is functional; the A copy in all humans is a pseudogene, i.e., it contains multiple mutations including an 8 bp deletion that would prevent its function. The corresponding A copy sequence of chimpanzee has been examined; it contains the same crippling 8 bp deletion seen in the human pseudogene (Kawaguchi, Am J Hum Genet 50:766-80, 1992). If the LCA is very far back up the tree, I suspect that mutations will make very old retroposons unrecognizable. == Artiodactyla (the group cattle belong to) and Cetacea (whales) have been evolving separately for quite a long time. The Last Common Ancestor of whales and cows probably lived sometime in the early Eocene, nearly 60 million years ago. == Crick _Life Itself, Its Origin and Nature_ == We have plenty of intermediates in the dino to bird transition. See: http://www.talkorigins.org/faqs/archaeopteryx/info.html http://www.accessexcellence.org/WN/SUA10/earlybird697.html http://www.cnn.com/TECH/9705/20/bird.dinosaur/ http://cas.bellarmine.edu/tietjen/images/missing_link_ties_birds.htm http://www.actionbioscience.org/evolution/benton2.html http://www.bulletin.ac.cn/ACTION/2002040302.htm How about Horses: http://www.talkorigins.org/faqs/horses/ http://www.flmnh.ufl.edu/natsci/vertpaleo/fhc/firstCM.htm http://chem.tufts.edu/science/evolution/HorseEvolution.htm http://www.talkorigins.org/faqs/horses/eohippus_hyrax.html How about whales: http://www.talkorigins.org/faqs/evolution-research.html#whale-legs http://www.neoucom.edu/Depts/Anat/whaleorigins.htm http://www.angelfire.com/fl/direpuppy/mindblocks.html http://www.indiana.edu/~ensiweb/lessons/wh.n.mkg.html http://www.cosmiverse.com/news/science/science05090201.html http://www.enchantedlearning.com/subjects/whales/allabout/Evol.shtml == Sarich, V. M., and A. C. Wilson. 1967. Rates of albumin evolution in primates. Proc. Natl. Acad. Sci. USA 58:142-148. Felsenstein, J. 1987. Estimation of hominoid phylogeny from a DNA hybridization data set. J. Mol. Evol. 26:123-131. Hayasaka, K., T. Gojobori, and S. Horai. 1988. Molecular phylogeny and evolution of primate mitochondrial DNA. Mol. Biol. Evol. 5:626-644. == The overwhelming evidence puts ducks and chickens together (Galloanserae), and penguins and pigeons together (Neoaves). == Robert Richards' _The Meaning of Evolution_ (Chicago 1992) == Organisms can and do adapt to their environment. A tree in the forest is tall and has most of its leaves at the top, whereas the same tree growing in an open field would be more rounded, probably shorter, and with more leaves on the lower branches. That is a form of adaption to the environment. What it cannot do, is pass its adaptions on to it progeny. == Correlation of growth. Darwin used this phrase to describe the observed phenomenon that a change in one part of an organism was often accompanied by change in another apparently unrelated part. Darwin correctly attributed this to unknown aspects of the the laws of variation on which his theory could say little. Law of reversion. Darwin used this term to describe the then-mysterious phenomenon of the reappearance of ancestral characteristics after many generations. == Retroviruses (and retrotranspon events more generally) do represent the conversion of genetic information in RNA into genetic information in DNA. However, this can be thought of as exchanging one type of genetic media for another slightly different one, rather than an altering genetic material on the basis of environmental cues. Even more interesting is the scrapie protein (similar to mad cow disease) which looked superficially like an infectious genetic protein. Upon closer inspection, however, it seems that it acts more like an aberrant self-assembling enzyme (causing normal protein to switch conformation to the scrapie conformation) than it does as genetic material. The scrapie protein has no effect on the DNA coding for the scrapie protein and is not transmitted to offspring (although there are DNA variants that code for proteins that have increased susceptibility to form the aberrant conformation). These DNA variants *are* transmitted to offspring. The only way the environment seems to influence the genetic construction of future generations is via selection. == Journal of Human Evolution == The probability of any single nucleotide mutating (point mutation) is about 10^-9/generation (with a rather wide range of variance). == Recessive traits like cystic fibrosis can be due to several hundred different individual variants or there can be 200 different forms of beta thalasemia (due to different deletions) in localized areas of the mediteranean == The English sparrows we have in the US today are desceded from a few introduced in New York in the late 1800's. They quickly spread over the continent. There are variations among populations in the US today. The ones in the north are bulkier, with more average as per unit of surface area, for instance. == Single stranded RNA is much more unstable than DNA, but double-stranded RNA is quite respectably stable. == In the molecular fate of the pseudogenes or the non-functional motifs; it illustrates what generally happens to the sequence whose function is no longer impacts positively on the fitness and thus falls out of favor with natural selection. What happens exactly depends on the particular sequence, but on average one finds a lot of mutations there, including the ones that are not tolerated in the functional sequences - stops, frame-shifts, mutations of the \conserved\ residues that play role in catalysis etc. After some (long) time we might no longer recognize the sequence original shape, as it deviates further and further from the functional ancestor, but it will linger around long enough for us to see a plethora of these sequences whose former function can be easily inferred. In other words, cellular genomes carry around not only the finished products, but also works in progress as well as the remains of already dead projects. == The better adapted an organism is to its environment the better the chance that such a large change would be harmful. No one in science believes that evolution took place in this fashion, and the genetic record bears this out. In fact, the extremely low probability of such mutations being successful is why creationists attempt to claim that evolution depends upon them. Punctuated equilibrium requires no such large mutations within a single generation. It simply says that over the time that a species exists (eons), changes within that species tend to occur over relatively short periods of time compared to longer times of relative stasis. A relatively short period to a paleontologist is a very long time == Biological evolution is a change in the genetic characteristics of a population over time. That this happens is a fact. Biological evolution also refers to the common descent of living organisms from shared ancestors. The evidence for historical evolution -- genetic, fossil, anatomical, etc. -- is so overwhelming that it is also considered a fact. The theory of evolution describes the mechanisms that cause evolution. So evolution is both a fact and a theory. See the Evolution is a Fact and a Theory FAQ, the http://www.talkorigins.org/faqs/evolution-fact.html Introduction to Evolutionary Biology FAQ and the Five Major http://www.talkorigins.org/faqs/faq-intro-to-biology.html Misconceptions about Evolution FAQ. http://www.talkorigins.org/faqs/faq-misconceptions.html#proof Evolution has been observed, both directly and indirectly. It is true. See the Five Major Misconceptions about Evolution FAQ. http://www.talkorigins.org/faqs/faq-misconceptions.html#observe Speciation has been observed, both in the laboratory and in nature. See the Observed Instances of Speciation FAQ and another FAQ http://www.talkorigins.org/faqs/faq-speciation.html listing some more observed speciation events. http://www.talkorigins.org/faqs/speciation.html == Evolution is defined as "the genetic transformation of popu