Fluctuating selection, canalisation, and evolvability: Why macroevolution is not “microevolution writ large”

30 04 2013

One of my biggest pet peeves is when people say that macroevolution is just “microevolution writ large”; this is a common saying especially among the creationist-debunkers to counter the claim that microevolution happens but macroevolution doesn’t. It infuriates me to no end, particularly because one of my biggest research goals is to identify the factors affecting the gulf between micro- and macroevolution, or why short-term microevolutionary changes do not accumulate to fixated and exhibited macroevolutionary changes.

And I’m not the only one who does this research, as this remains one of the most open questions in evolutionary biology (Arnold et al., 2001). Part of the problem is that environments change all the time, and with them change the selective optima – what may be the most fit phenotype at one point in time might be the most unfit several generations later. The leads to a pattern of fluctuating selection, where the optimal phenotype(s) change every so often.

Fluctuating selection is generally agreed on as a factor in the evolution of evolvability (Wagner & Altenberg, 1996), the ability to maintain a high rate of microevolution, which in turn is dependent on the concept of canalisation first espoused by Waddington (1942). While he was talking about it in terms of development and evo-devo, we co-opt it in this discussion to talk about population genetics, since that’s the framework for microevolution. Wagner et al. (1997) define it under this framework as an effect leading to the lessening of the effect of mutations.

In other words, by decreasing canalisation, you increase evolvability, since evolvability demands the ability to produce new effectual mutations (Moreno, 1994). This then links back to fluctuating selection because in order to respond to a regime where the optimal phenotype changes constantly, higher evolvability and less canalisation is needed. Studies show exactly this: under fluctuating selection, decanalisation alleles and polymorphic genes become selected for (Kawecki, 2000), i.e. evolvability rises as expected.

An analogous way to consider this is by thinking about how parasites and other highly-specialised organisms (highly-canalised organisms) tend to reach evolutionary dead-ends, while generalists can always specialise further (highly evolvable).

That analogy brings us back to the phenotype and the bridge to macroevolution. Consider that microevolutionary changes, over many generations, are basically subject to cycles of fluctuating selection. If we generalise that fluctuating selection leads to higher evolvability and thus a higher amount of effective mutations, that means that the genotypes generated by generations of microevolution are geared towards producing variability, which then translates to a higher diversity of phenotypes. This is why we can’t say that macroevolution is microevolution writ large: by doing so, we imply that macroevolution is canalised by microevolution, when microevolution does not undergo canalisation except under strict and consistent selectionist regimes.

And even then, the implication that the genotype is a precise blueprint for a single morphology is false, since it ignores the various filters put in place by development and phenotypic plasticity. So, in all, please don’t say that microevolution is equal to macroevolution. They’re different fields (and they’re taught separately: any good evolution program will have a specific course on macroevolution and another on microevolution), they involve different phenomena, and the process of evolution is different at both levels. This is why we talk of a bridge between micro- and macroevolution: there is a chasm to be crossed. Macroevolution is not merely the magnified version of microevolution.

References:

Arnold SJ, Pfender ME & Jones AG. 2001. The adaptive landscape as a conceptual bridge between micro- and macroevolution. Genetica 112-112, 9-32.

Kawecki TJ. 2000. The evolution of genetic canalization under fluctuating selection. Evolution 54, 1-12.

Moreno G. 1994. Genetic Architecture, Genetic Behavior, and Character Evolution. Annual Review of Ecology and Systematics 25, 31-44.

Waddington CH. 1942. Canalization of development and the inheritance of acquired characters. Nature 150, 563-565.

Wagner GP & Altenberg L. 1996. Perspective: Complex Adaptations and the Evolution of Evolvability. Evolution 50, 967-976.

Wagner GP, Booth G & Bagheri-Chaichian H. 1997. A Population Genetic Theory of Canalization. Evolution 51, 329-347.





Rise of the Evolutionary Theory

29 04 2013

This guest post is written by Jessica Reynolds, who loves all aspects of science, especially anthropology and archaeology. After obtaining a degree in anthropology she decided to give up her trowel in favor of pursing writing. She currently writes about various scientific topics, including resources for students who need a scientific poster or other resources for research projects and presentations.

Evolution is always a hot topic in the scientific world and Charles Darwin is the man seen at the forefront of it all due to his explanations of natural selection. While Darwin did play a large role in the explanation and implementation of evolutionary theory, he was not alone in creating the largest paradigm shift known throughout history. Natural selection and other key components of evolutionary theory have a long history of important figures whose ideas are often overlooked. The beginnings of selectionist ideas and advances in racial science set the standards and methods that make up how evolutionary theory is seen today, especially in regards to humanity.

During the seventeenth and eighteenth centuries, questions about the physical and cultural differences among people of various populations were widely debated among scholars. These question sparked many different ideas and theories concerning variation among populations.

Monotheistic and Polytheistic Views

The monogenesis and polygenesis origin debate stemmed from these questions and are the frameworks in which possible explanations are developed. Monogenesis is of the belief that there is only one origin of humans. Joseph-Francois Lafitau suggested a theory of degeneration where human populations all started out the same but have “fallen from Eden”. The reason for differences in populations is because some have fallen farther than others and different populations fall in different ways. Lewis Henry Morgan embraced a monogenist view in a slightly different light. He suggested that human populations rise as oppose to fall and some populations have risen closer to perfection than others.

Polygenesis is the counterpart to monogenesis and is the belief of multiple human origins. In a polygenesis context, differences in physical and cultural characteristics are seen as a deficiency – not everyone is created equal. Ellsworth Huntington suggested that people are physically different based on the geographic and climatic factors of the environment. These factors not only affect the physical characteristics of a population but the cultural characteristics as well. Jean Bodin’s ideas on the difference between Northerners and Southerners only enforced this idea.

Racism Setting the Standards

Because of ideas like Huntington’s, racism prevailed, even among those who had a reputation for advocating human rights, and becomes a backdrop to evolution. Thomas Jefferson, for example, believed that all men were created equal but he only applied this standard to white men. Therefore he believed that black people were inferior to whites and continued to own slaves throughout his life.

Scholars such as Johann Blumenbach argued for white supremacy but racists rarely tried to link their racist ideas with scientific reasoning. The few attempts of racists to use scientific reasoning, however, have led to the first methods and standards of science which are crucial in evolutionary thinking. Adolf Retzius and his invention of the cranial index, which is a formula for measuring the head, had set the standard for which racial science should be conducted in.

Tracks of Evolution Development

Alongside racial science, evolutionary theory was developed by following three tracks; biological, geological and historical. It is suggested that Darwin pulled the ideas articulated in On the Origin of Species from ideas of various scholars that followed these three tracks.

There were several figures who laid out the framework for evolutionary theory along a biological track. Louis Agassiz introduced three fold parallelism which says that embryonic variability, as well as variability among adult forms, must be identified and then the gradation along a timeline must be configured. Herbert Spencer, who is in some cases considered the father of sociology, coined and described the term survival of the fittest. This is the first time fitness is even taken into consideration in regards to evolution. Perhaps the biggest contribution on the biological track to the evolutionary theory though is Thomas Malthus’s Essay on the Principles of Population. It is in this essay that selection and the struggle to survive is introduced.

Geographic analysis published by various figures also influenced Darwin’s work. Jean-Baptiste Lamarck publishes Hydrogeology in 1802 in which he argues that the earth is several billions of years old. 31 years later Charles Lyell published Principles of Geology which takes on scriptural authority and was the first major formal critique of Lamarck. He rejects Lamarck’s work because he sees it as a theory of perfectibility.

Lamarck invented many of the terms we use today in regards to animal classification. You can learn more in this previous post about Lamarkism.

Charles Darwin, Himself

It’s not surprising that such a large shift in thinking did not happen because of one man and it’s true that many people were involved in causing such a shift. All the same, Charles Darwin has been known as the Father of Evolution and rightly so. Had it not been for On the Origin of Species, evolution may have taken a completely different trajectory and more misconceptions regarding evolution could have manifested themselves. In On the Origin of Species, Darwin explains natural selection as a random process as opposed to upward mobility of a species.

The public view of evolution has shifted due to many factors, not all of them scientific. The early history of evolution in regards to race was often used to justify racism. Social aspects also include religion, of course, since many sacred texts do not refer to the process of evolution or allow for enough time for evolution to take place in their historical accounts of Earth’s existence.

Even the scientific study of evolution has so many factors (geological and biological being the main ones) that it is difficult to narrow down even a specific aspect of evolution to one discovery or discover. This is why it is important to give names and voices to those scientists, writers, and texts that have formed evolutionary theory as it exists today and is refined and explored further in the future.





Papers of the Week: 22.04 – 29.04.2013

29 04 2013

Papers from the past week. [OA] are open access. Feel free to request a detailed discussion on any of these.

General Interest, Important:

Vivisection, the practice of dissecting living organisms for scientific study, is nowadays mostly frowned upon for bioethical reasons. We can study anatomy when the animal is dead, and there are many technologies available to allow us to non-invasively study physiological systems, so there is no major reason to do vivisections anymore. These technologies haven’t always been here though, and a lot of the early biological sciences were filled with accounts of vivisections, which did bring about a wealth of knowledge, so they weren’t wasted (or for fun, as animal rights terrorists would have you believe). This special issue has several papers on the growth of vivisections during the early times of this period, the 16th and 17th century.

There are two interesting and important aspects to this paper. The first is the insights into the endosymbiosis that led to the eukaryotes. The second is the one I am more interested in, and that’s the power of phylogenetic networks over phylogenetic trees. We have many phylogenetic trees of eukaryotes, but it was only with this paper and their employment of a network that we could clearly see the presence of the endosymbiosis, since a tree can only show one set of relationships – detecting things like endosymbioses and organismal fusions is simply beyond the scope of a phylogenetic tree, since a tree portrays hierarchical relationships where genes are passed vertically from parent to offspring, whereas an endosymbiosis is a relationship where genes are passed horizontally between unrelated organisms. Networks have no problem with such things, and can portray hybridisations, endosymbioses, reticulations, and other such phenomena that don’t fit into the standard basal-to-derived branching scheme of a phylogenetic tree. This paper is an example of this.

It’s well-accepted that science needs to play a dominant role when deciding how to deal with issues such as climate, not only because meteorology is a scientific discipline, but also because the scientific method has built-in mechanisms to check up on the effect of such policies and modify them as needed. Case in point: this paper, which examines how current climate policies are faring in the overall picture, if they are really working towards keeping the damage to a minimum or whether they’re just useless. We will not see the results of our work until at least the 2030s, according to the paper, and the conclusion is a rather obvious “the sooner the policies get to work, the better”, since a constant result is that the sooner emissions peak, the fewer the damages will be in the long run.

I recently wrote a tiny bit on bryozoan placentas, so here’s a paper with much more information.

G-quadruplexex are structure formed at the end of telomeres. Telomeres are repetitive DNA sequences at the end of chromosomes that get eaten away through the cell’s lifespan, acting as decoys so that the useful chromosomal DNA doesn’t get damaged. When you have four of them next to each other, they will fold with each other and form the G-quadruplex (G4). The G4 acts to stabilise the telomeres, and so have been actively researched over the past few years because telomere degradation is heavily implicated in cancer and ageing. It was also recently found that G4 complexes are found in other regions of the DNA molecule, not just at the bookends of it. If any of this stuff sounds interesting, this paper has a great summary of it all, and it also delves into a pretty cool discussion of how the genome ought to be viewed as a complex landscape rather than just a string of ATGCs. This biochemical stuff isn’t my cup of tea, but it’s interesting stuff anyway. Read the rest of this entry »





Spider Vision

27 04 2013

This is a requested post on the basics of spider eyes; for more on spiders, check out my spider lecture.

Spiders only have ocelli, simple eyes consisting of a lens covering a vitreous fluid-filled pit with a retina (pigment cells + visual cells) at the bottom. The ocelli come in two types: the main eyes and the secondary eyes.

Eyes in spiders are named after their respective position on the head. Therefore, we distinguish between the following:

  • Anterior median eyes: front, center;
  • Anterior lateral eyes: front, side;
  • Posterior median eyes: back, center;
  • Posterior lateral eyes: back, side.

The anterior median eyes (AMEs) are always the main eyes, present in all spiders except the Dysderidae, Sicariidae, and Oonopidae. You can easily recognise them in pictures because they’re black, a consequence of not having a tapetum that reflects light back out. Main eyes are fairly uniform in all spiders and differ in their structure from secondary eyes in that they’re everted eyes – the light-sensitive parts of the retina (the rhabdomeres) are pointed towards the light.

All the rest of the eyes are secondary eyes. Secondary eyes are inverted, with their rhabdomeres pointing away from the light, same as in vertebrates (including the human eye). The number and arrangements of secondary eyes can differ significantly, as can their structure: for example, a typical garden spider has lateral eyes with a tapetum, while median ones lack it. All of these differences mean that secondary eyes are incredibly useful for taxonomic purposes, and it’s often so that merely looking at the eyes of a spider will give you a reliable identification of its family.

These differences result in highly-variable image qualities, and have most probably evolved due to ecology. Large secondary eyes can contain several thousand rhabdomeres, resulting in very high sensitivity to light that is very useful to hunters and/or nocturnal spiders. In contrast, small secondary eyes contain a couple hundred rhabdomeres at best, rendering them fairly useless for much beyond movement detection, which is why web-building spiders tend to have them: they don’t need fancy eyes for hunting.

Main eyes are immobile, small, and have a short focal length, granting the spider a large depth of field, making it unnecessary for them to have a focusing mechanism for short ranges. The best main eyes are found in salticids and thomisids, where they are enlarged, resulting in a clear, crisp picture.

This pictures is then combined with the 3D perspective given by the mobile and widely-spread secondary eyes in order to allow the spider to judge distances, most useful for hunting or ambushing spiders.





François Jacob (1920-2013)

22 04 2013
François Jacob. Source.

François Jacob. Source.

François Jacob (1920-2013) is pretty much a household name for biologists. He was a French molecular biologist who was one of the three 1965 Nobel Prize in Physiology or Medicine winners (the other two were André Lwoff and Jacques Monod). Monod and Jacob got it for their work on the lac operon, which laid down the foundations for the study of the mechanisms behind gene regulation and expression. He died 3 days ago. Carl Zimmer already has an excellent article on him, but it doesn’t hurt to help spread his legacy around. I’m sure many of the obituaries will concentrate on the molecular biology he is most famous for, so I want to take a different tack and discuss his contribution to evolution through his highly-influential 1977 Science paper, Evolution and tinkering.

In it, he introduced the world to the concept of gene co-option. Co-option of morphological traits had been well-known, but it was Jacob who showed that “evolutionary tinkering” can occur also at the genetic level, with old genes being repurposed to serve new functions.

Jacob’s envisioning of how this would work stems from his previous work on gene expression and regulation. Instead of requiring completely new genes to produce novel morphologies, genes can simply be controlled by regulator genes. These can have slight changes in activity, which results in the target genes being switched on and off at different times during development, leading to new morphologies at the end. If the new morphologies are successful, then the new pattern of regulatory gene activity is automatically selected for, and the new morphology is retained.

In other words, an important source of morphological novelty can come from evolution “tinkering” with pre-existing systems. It’s similar to cooking: if you’re frying a piece of chicken, adding onions at the start of the frying, in the middle, or at the end of the frying will produce very different flavours (burned vs. caramelised vs. raw). Similarly, if your regulatory gene does its thing at the 4-cell stage, at the start of gastrulation, or the start of neurulation, the end result will be pretty different in each case. Of course, things are more complex in real life, since location and co-interactions also come into play, but I’m simplifying to illustrate the point.

The existence of such mechanisms is now routine knowledge, and examples are present in any evolution and developmental biology textbook, as it’s an important concept for evo-devo.

He did go a bit too far in arguing his case when he claimed that “the probability that a functional protein would appear de novo by random association of amino acids is practically zero”, which is factually wrong (linked is just one random example). In all fairness though, at time of his writing, it was probably a sensible claim to make since there were no examples, so we can’t fault him for it.

That paper was also a rather philosophical one on the nature of evolution, and is an excellent text to use against Intelligent Design creationists with its description of how natural selection is constrained by historical contingency, forcing it to work by tinkering rather than by following a preconceived plan as a designer would. It also contains some excellent quotes and passages on the nature of science itself. Here’s one of my favourites:

[Science] operates by detailed experimentation with nature and thus appears less ambitious, at least at first glance. It does not aim at reaching at once a complete and definitive explanation of the whole universe, its beginning, and its present form. Instead, it looks for partial and provisional answers about those phenomena that can be isolated and well defined. Actually, the beginning of modern science can be dated from the time when such general questions as “How was the universe created? What is matter made of? What is the essence of life?” were replaced by such limited questions as “How does a stone fall? How does water flow in a tube? How does blood circulate in vessels?” This substitution had an amazing result. While asking general questions led to limited answers, asking limited questions turned out to provide more and more general answers.

If you want to read more about him, what better way than to read what he wrote himself? He has a very interesting autobiography from 1988, highly-recommended: The Statue Within: An Autobiography.

References:

Jacob F. 1977. Evolution and tinkering. Science 196, 1161-1166.

Jacob F. 1988. The Statue Within: An Autobiography.

Li C-H, Zhang Y, Wang Z, Zhang Y, Cao C, Zhang P-W, Lu S-J, Li X-M, Yu Q, Zheng X, Du Q, Uhl GR, Liu Q-R & Wei L. 2010. A Human-Specific De Novo Protein-Coding Gene Associated with Human Brain Functions. PLoS Computational Biology 6, e1000734.





Papers of the Past 20 Days: 02.04 – 21.04.2013

21 04 2013

It’s been a while, but I’ve kept them all the papers stored in a tab, nothing is lost. [OA] indcates open access papers. Feel free to request a detailed look at any of these.

General Interest, Important:

It’s no secret that I hold a low opinion of a lot of the human sexual selection and evolutionary psychology research, because I see a trend of insufficient sampling leading to overgeneralised statements that resemble “just-so stories” rather than evidence-backed claims. Here’s one paper that shows how to critically examine such papers.

Check out the whole range of additions, replies, and commentaries here, all [OA].

Tangentially-related, this review paper: Animal personality: what are behavioural ecologists measuring?

I always like to feature experimental evolution, especially when the results are as cool as this. Evolving multicellularity artificially isn’t anything new (e.g.), but more successful repetitions lead to us being able to identify all the potential evolutionary pressures that could have led to the convergent evolution of multicellularity, so such studies should always be encouraged.

Of course, studying things phylogenetically is also a good way: Development of ichthyosporeans sheds light on the origin of metazoan multicellularity [OA].

A point I made in my oft-read post on animal intelligence is that relative brain size is a fairly irrelevant criterion for intelligence. What matters more is organisation and connections between brain areas. While I was basing it on insects, the generality does also apply to mammals and vertebrates, as this paper shows: mosaic evolution is what leads to specialisations in the brain, and it’s what leads to the varying cognitive abilities of animals. Mosaic evolution in this case means a faster rate of evolution in some brain areas, which would automatically lead to novel connections. Relative brain size itself is irrelevant.

Some more on brains: Deep Homology of Arthropod Central Complex and Vertebrate Basal Ganglia.

I’ve written before on what I think of most genome sequencing projects: largely meh. This is a case of a non-meh genome sequencing project, since it showcases the depths of adaptation in obligate parasites. As an invertberate zoologist, I’m intimately familiar with their various morphological contrivances, but what this genome project shows is that they are accompanied by fancy genomic specialisations too. That’s my main interest, although less hedonistic scientists would be interested in the medical advances enabled by these discoveries.

Of course, the genome that everyone was concentrated on this week was the coelacanth. I have no idea why, it must be that idiotic “living fossil” myth. Whatever. Here’s a link to it: The African coelacanth genome provides insights into tetrapod evolution [OA].

It’s of narrow interest, but thought I’d highlight it as shameless self-promotion: this is the sort of thing I wanted to do with arthropods when I came to Cyprus, but failed as a result of never receiving any funding.

One of the points I tend to stick on when teaching evolutionary theory is the effect of population size. Very generally, the role of genetic drift (random evolution) gets larger as populations get smaller. Very large populations have their own wacky processes going, which this paper reviews and tells us to study deeper. I agree.

The Lessepsian migration is one of the more fascinating large-scale ecological phenomena happening nowadays. Since the Suez Canal was opened, the fauna of the Red Sea has been migrating naturally into the Mediterranean and, surprisingly, they’ve been outcompeting and displacing the native Mediterraneans. You can read some proposed reasons why in this paper. On a general note, I use this example to show that the distinction of “native” and “indigenous” ecosystems, while very useful for conservation, is not an evolutionary one. It’s a historical one, but just because species have evolved in the same place for centuries and millenia, it doesn’t mean they are a “perfect fit” – and this isn’t something we should expect anyway.

A slight ray of hope? Eh, depends on your perspective. Coral reefs may be among the most fragile of ecosystems, but this status is, in my opinion, very reflective of the disproportionate amount of attention that coral reefs get both from studies and from human anthropogenic disturbance – coral reefs get visited a lot, just look at any tropical tourism leaflet. This is what this paper shows, again in my opinion: leave coral reefs alone and they will rebound. Of course, ocean acidification is another problem altogether, but solving that is slightly more complex than slapping tourists and naughty fishermen around.

More coral research from this time period: Calcification by Reef-Building Sclerobionts [OA].

One of the biggest perks of being an invertebrate biologist is that you have the opportunity to learn and observe an enormous diversity of animal life. It’s much nicer than just being restricted to stupid mammals and birds and lizards and fish. It’s also great if you’re an educator, because kids tend to be informed only of charismatic animals: pandas, rabbits, cats. But this is a way too blinkered and narrow view of biodiversity, so introducing kids to the whole gamut of animal life is very satisfying. Here’s a review for the placozoans, the simplest animals yet known with only 5 cell types, with only one species officially described, Trichoplax adhaerens. It’s a marine 2mm large disc-shaped blob that constantly changes shape, and is more or less invisible in the wild – you need a stereoscope to see them properly. Go to www.trichoplax.com for pictures!

For another bunch of weirdo invertebrates: Molecular phylogeny of kinorhynchs; A complete three-dimensional reconstruction of the myoanatomy of Loricifera: comparative morphology of an adult and a Higgins larva stage [OA].

Another paper from this “Global Diversity” series from this time period, but involving stupid vertebrates: Global Taxonomic Diversity of Living Reptiles [OA].

I’ve already written about this very cool field of research, the study of plant-arthropod interactions through time and the useful info we get out of it. Here’s a review from the Grand Master of the field.

New genes can arise fortuitously, but their gaining a fitness-affecting function is a more advanced prospect, and their fixation a rare event indeed, since the new genes must be integrated into the whole of the organism where domino effects, pleiotrop, and general chaos rule. This paper sketches a pathway for all those.

One of my favourite aspects of developmental biology is the mechanical, physical basis for it: the effects of cells bumping into each other, the effect of cells moving through fluids, even the effect of gravity. Genes and developmental pathways are cool and all, but I have a special affinity for such holistic, big-picture perspectives that take external complicating factors into account. This paper provides an example of how important such things can be.

I think Easter is happening around now, not sure though. But I do remember writing a popular post on regeneration one year for Easter. Planarians feature heavily in it, and this review is useful if you want more details on why planarians are useful for the study of regeneration, and a historical perspective.

Horned beetles are a classic model system for evolutionary ecology and evo-devo (and later will be for eco-evo-devo, or whatever the abbreviation will be). The interest arises because beetle horns are completely novel structures that arose convergently 6 times in beetles and were meaintained. Development informs us of how a novels tructure can arise in the first place; ecology tells us what they’re used for; evolution tells us how they remain. Put all that together, and you have a fascinating model system you can with hundreds of studiable species and permutations. This paper reviews all this potential.

If the meshing of evolution and ecology interests you, then so will this: Special Issue: A Critical Look at Reciprocity in Ecology and Evolution.

Crazy people with an agenda call us who follow the science on global warming “alarmists”. Here’s a paper to shove in their faces. Although the assumption that they know how to read is unwarranted and not backed up by the evidence.

China is the gift that keeps on giving in palaeontology. Some more amazing fossils.

But hey, other countries with cool fossils still exist: A ten-legged sea spider (Arthropoda: Pycnogonida) from the Lower Devonian Hunsrück Slate (Germany); A troodontid dinosaur from the latest Cretaceous of India; Original spotted patterns on Middle Devonian phacopid trilobites from western and central New York; A Large Accumulation of Avian Eggs from the Late Cretaceous of Patagonia (Argentina) Reveals a Novel Nesting Strategy in Mesozoic Birds [OA].

There’s been much fuss made about this in the popular science news. I took care of it on request some time ago on the Facebook page of the blog, so I’ll just copy-paste the text from there. It’s a solid phylogenetic study of mites whose main result is that dust mites are belong to a group of mites parasitic on vertebrates. In other words, house mites evolved from a parasitic ancestor. This is deemed surprising because parasites are rightly considered to be highly-specialised, so while a transition from generalist to specialist is easy to envision, the opposite is more implausible. But implausible is not impossible, as this study shows. The way the article is reported on belies the true nature of the advance here, especially witht he invocation of Dollo’s Law (which, to be fair, was done by the original authors as well). Dollo’s Law, as understood today (which is a far cry from Dollo’s original formulation), refers to a proposition that single complex characters, once lost, cannot be regained. But its validity as a law is increasingly being called into question, as more and more evidence piles on against its validity (see this paper, for example, which shows that fingers revolved in several liazrds even after they were evolutionarily lost). Saying that this paper puts “a new piece in the evolution puzzle” is just plain wrong. That piece has been known for ages. And in any case, a violation of Dollo’s Law is emphatically not “reversible evolution”, because that implies that evolution has a direction. The discovery is that the linear evolution to the free-living dust mite went like this: Free-living mites -> parasitic mites -> free-living dust mites. Does this mean that, somehow, dust mites have suddenly gone back in evolution? Absolutely not, because that would imply that they are now identical to those free-living ancestors of the parasitic mites. They’re not. They’ve gone their own way in evolution. So, to summarise: the awesome finding here, beside the details about mite evolution, is that free-living organisms can evolve from specialised parasitics. It’s not a reversal in evolution, except in the sense that their ecology is now similar to that of their distant ancestors. There is no such thing as “devolution”.

Those with a memory good enough for two years will remember the huge splash from two years ago from the description of Australopithecus sediba. For the uninitiated, enjoy a description I had written that time: They found pieces from two individuals: a 12-13 year old male, and an adult male. The age of the find is 1-98 – 1.75 million years, a time when there were many other hominins running around. The one closest to A. sediba, morphologically, is A. africanus: the body is very similar, with both being bipedal, but still having long arms (adaptation to trees). The face is also pretty much identical, besides A. sediba having slightly smaller teeth and more flattened cheeks. This is excellent, because A. africanus disappears from the fossil record before 2 Ma, so A. sediba fills in perfectly as their descendant, and so we get some more resolution of the australopithecine tree. A. sediba‘s hips have some feature found in Homo erectus, but not found in H. habilis and H. rudolfensis. The authors interpreted that as meaning that A. sediba is either ancestral to Homo (or very close to the ancestor), and that H. habilis and rudolfensis are not Homos, but actually australopithecines. Maybe I missed it when skimming through the paper, but I didn’t see them discuss the possibility that it’s convergence. After all, the hips are both adapted to bipedalism. It’s not far-fetched to think that they will look similar, and come up with the same mechanisms, to enable that. They then go into various arguments about Homo habilis not being a human ancestor, bringing in punctuated equilibrium to the mix. The whole issue has to do with how early Homos and australopithecines fit together – something that will always be controversial.

In any case, another big splash has been made, with another special issue devoted to A. sediba, with more papers with more detailed analyses and claims. Take your time poring through them, this is pretty critical stuff!

The phylogenetics and classifications of unicellular eukaryotes is something that invertebrate biologists are supposed to be familiar with, but I never had the interest in the microthings and don’t keep as close an eye on the advances as I should. Good thing reviews exist.

Something for the archaeologists.

Only putting this here because it has personal significance for me: the Nördlinger Ries is the very first impact crater I went to as a student. Long-time readers should also be familiar with it: it’s the big brother of the Steinheim crater, where the lake that contained the Steinheim snails was. In fact, that post is a simplification of the field trip report I had to write when we visited the Nördlinger Ries. Ah, to be 6 years younger again. Good old days. Hmm. Read the rest of this entry »





Reading List: Human Evolution papers

20 04 2013

The following is the reading list I would give to a typical undergraduate human evolution course. The purpose is not to give the students papers with the descriptions of every new fossil species (a perusal of Wikipedia can get you all their names), but to provide a comprehensive overview of the breadth of human evolution research beyond the palaeontology, as well as general reviews that may be dated – a critical skill for any science student is to be able to dig out advances that have happened since the publication of a paper and put these advances within the general research context.

Sorted alphabetically by author, not by importance. Links lead to abstracts, privately-hosted PDF links also included. You can batch download all papers from this Dropbox folder. Also check out the listing of recommended books on human evolution.

Papers:








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