group selection

topic posted Mon, March 10, 2008 - 6:24 PM by 
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come on, what's the hubbub? the currency of inheritance is almost always the gene, and sometimes a gene is affected via a group all at once. what's the controversy here? big deal. the gene is the bottom-line unit of selection, but genes can be affected simultaneously among different bodies in different copies. isn't that the deal? david sloan wilson drives me a little batshit, frankly, and dawkins seems not ready to give an inch on his "the gene is the unit of selection" mantra. dawkins is right, but genes can be selected for via groups. just what in the hell is the big controversy about here? sorry to bring this up yet again. just saw sloan wilson's presentation at beyond belief 2, and was irritated.

thesciencenetwork.org/BeyondB...2/watch/

his is supposedly a direct rejoinder to dennett's presentation, but really doesn't amount to one.
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  • altruism not a family matter?

    Mon, May 26, 2008 - 3:08 PM
    Altruism is no family matter
    12 January 2008
    From New Scientist Print Edition. Subscribe and get 4 free issues.
    Daniele Fanelli

    IT IS just about the greatest sacrifice possible, and in evolutionary terms it looks like madness. Forgoing reproduction in order to help raise another's offspring is a supreme act of altruism. It happens routinely in hundreds of ant, bee and wasp species, where sterile workers toil for the benefit of the queen.

    For the last 40 years, the evolution of such altruism has been explained by kin selection: the idea that helping your relatives - and therefore helping spread the genes you share with them - outweighs the cost of not having offspring of your own. It's the genes that matter, not the individuals in which they reside or the groups in which those individuals live. The idea was encapsulated in Richard Dawkins's pervasive metaphor of the selfish gene.

    Now, in a move that has baffled evolutionary biologists worldwide, the father of sociobiology and the world expert on social insects, Edward O. Wilson, says insect altruism and colonial living do not after all require kin selection to evolve (BioScience, vol 58, p 17). Instead, he cheerfully says, it only requires a small "hop": "One small step for a wasp, one giant leap for hymenoptera."

    Lightly said, but Wilson's ideas, if proved correct, would have great consequences. Altruistic behaviour was at one time a Darwinian paradox: how could the individual struggle to survive and reproduce favour such a strategy? The solution became known as Hamilton's rule (see "To die for two brothers"). It explains, for example, why fertile females in many species of bees and wasps cooperate in reproduction instead of nesting alone. It also explains why castes of permanently sterile workers evolved. Or does it?

    Wilson, who is at Harvard University, points out that eusocial behaviour (where a mother "queen" is assisted at the nest by non-reproducing offspring) has been discovered in a variety of organisms. Species of aphids, shrimps, beetles, naked mole rats and others have joined the club. They have many ecological traits in common - in particular a large nest that must be defended from parasites or predators - but very different genetic structures. Naked mole rats, for example, have two sets of chromosomes - making them diploid, like us - and reproduce sexually, also just like us. Aphids, on the other hand, form colonies of genetically identical clones. In aphids, therefore, one might expect altruism to be particularly common, but it is not. These and other observations led Wilson to conclude that kin selection was not the decisive factor in the evolution of sterile workers (see "Kin selection: for and against").

    “Aphids form colonies of identical clones, so you might expect altruism to be particularly common, but it is not”

    Flexible lifestyle
    Eusociality, argues Wilson, emerges from a rare combination of life-history characteristics and pre-adaptations. In particular, it can only evolve after the insect has gone through a phase where it can be flexible in its behavioural choices. For example, females of a solitary wasp species occasionally take the role of either "queen" or "worker" when forced to nest together. If an environmental change or a new mutation then inhibits the dispersal of their offspring, they will be forced to stay at the natal nest. The pre-adaptations enable them to cooperate efficiently. Thus, says Wilson, fully eusocial colonies emerged in one single leap, and went on evolving by means of group selection, because groups that cooperate do better than those that do not.

    Wilson's "flexibility" scenario for the evolution of eusociality in insects is not new. A similar idea was proposed as an alternative to kin selection about 30 years ago by Mary Jane West-Eberhard, now at the Smithsonian Tropical Research Institute in Panama. She, however, no longer sees flexibility as incompatible with kin selection. "In fact, [it] depends on kin selection to work," she says. "Hamilton's rule describes the precise switching point when the flexibly responsive females should stay in the groups and express costly worker aid."
    Wilson's downgrading of kin selection theory, however, goes beyond its role in eusocial evolution. Kin selection "is not wrong, and it is internally consistent, but it is ineffective", he says. "If you look at the literature of the theory, there are a lot of impressive-looking mathematical models but they scarcely ever come up with a real measure of anything that can be applied to nature."

    Most evolutionary biologists New Scientist spoke to strongly disagree. "I think he has rather underestimated what kin selection theory has achieved," says Andrew Bourke of the University of East Anglia, UK.

    "We are finding it useful in studying microbes," says David Queller at Rice University in Houston, Texas. "It turns out that when they are altruistic they are related too. We weren't too surprised, because that is a prediction of kin selection theory."

    Kin selection theory "makes all kinds of predictions about social behaviour", adds Francis Ratnieks of the University of Sheffield, UK. Since many of these predictions have been supported, he says, we can be confident in it.

    Wilson's forthcoming book The Superorganism, written with Bert Hölldobler of Arizona State University in Tempe, will further advance the case for eusociality evolving by group selection in a single leap. "It's essentially a new paradigm," he says. However, the two theories might turn out to be compatible.

    "Sociobiologists used to think that group selection was completely wrong, and some people still think that way," says Queller, "but a large number of us think that group selection, if you do it correctly, is just alternative language [to kin selection] for describing social evolution."

    All researchers agree, though, that there is more to social behaviour than just kin selection. To understand social evolution "we have to look at phylogeny, at gene expression, at anatomy, at behaviour, at ecological context", says James Hunt of North Carolina State University in Raleigh.

    In a nod to the "modelling industry" that has sprung up around Hamilton's rule, Ratnieks concedes that sometimes models were developed in the absence of biological data. "These models almost had a life of their own, with underlying assumptions that in many cases were never verified."

    Most sociobiologists say Wilson's ideas don't herald a scientific revolution. "Kin selection theory has always had its detractors," says Bourke. "Its critics have seen it as too reductionist, too genetical, perhaps even too Dawkinsian, or they just got bored with it because it became so dominant."

    Wilson is not surprised. "Of course they are going to remain critical for a while," he says. "I am used to taking the heat, and in the past I turned out to be right. If those who defend the standard theory come back in lucid terms and show, point by point, why these hypotheses are already understood, I'll be glad to concede. But I haven't seen any evidence yet. Maybe they will now."
    • Here's dawkins' reply to the article about wilson's invocation of group selection explaining the evolution of colonies:

      "EDWARD WILSON has given us a characteristically fascinating account of the evolution of social insects (see "Kinship doesn't matter - how insects are altruistic" and BioScience, vol 58, p 17). But his "group selection" terminology is misleading, and his distinction between "kin selection" and "individual direct selection" is empty.

      What matters is gene selection. All we need ask of a purportedly adaptive trait is, "What makes a gene for that trait increase in frequency?" Wilson wrongly implies that explanations should resort to kin selection only when "direct" selection fails. Here he falls for the first of my "12 misunderstandings of kin selection"; that is, he thinks it is a special, complex kind of natural selection, which it is not.

      “Edward Wilson thinks kin selection is a special, complex kind of natural selection, which it is not”
      In the true sense of kin selection, offspring are "kin" just as siblings are. Parental care and sibling care both evolve because copies of genes for caring are present in beneficiaries. Genes promoting feeding of larvae by sterile workers are passed on by those larvae - sisters, nephews, and so on - destined to become reproductives. That's kin selection, and it maintains sterile worker castes in insect colonies. Wilson could not dispute that.

      What he does dispute - perhaps correctly - is that eusociality originated through related females clubbing together because of kinship. It could also originate through unrelated females nesting together. But to call this "group selection" is massively confusing. A better approach is John Maynard Smith's concept of evolutionarily stable strategies (ESS). "Stable" means that when most individuals follow the strategy, no alternative does better. If "breed cooperatively" were a stable strategy for unrelated females, this would furnish a good preadaptation for the evolution of eusociality.

      Jane Brockmann, now at the University of Florida, Gainesville, and I explored this with an ESS model developed with Alan Grafen of the University of Oxford, using Brockmann's fieldwork on solitary digger wasps, Sphex ichneumoneus. When following the "dig" strategy, a female digs a burrow, provisions it with prey on which she lays a single egg, seals the burrow and departs. But burrows may be abandoned and this opens the way for an alternative strategy: "enter" an existing burrow and take it over, saving the time and effort of digging. The disadvantage is that the original owner may not have abandoned the burrow, and you run the risk of a dangerous fight. So the decision whether to enter or dig is a gamble.

      With too much entering in the population, not enough new burrows get dug and chances rise that a given burrow will be occupied. Selection would therefore favour digging. With too much digging, many abandoned burrows go begging, and individuals should enter instead. Grafen's ESS model predicted an equilibrium frequency of digging versus entering with equal benefits to each. Brockmann's field measurements were rich enough to test this prediction, and it was, with reservations, fulfilled.

      Brockmann and I then postulated an ecological "landscape" over which the parameters governing Grafen's model might vary. A change in ecological conditions might move digger wasps from an "aggressive space" strategy, as used by S. ichneumoneus, to "tolerant space" - where diggers benefit from being joined by an enterer. From here there is a smooth gradient to "cooperative space", where both parties benefit from sharing. Our review of the literature uncovered wasp species that apparently take such intermediate positions. From here, the evolutionary journey to full eusociality is easy.

      Revealingly, Wilson's great book Sociobiology allots only four sentences - in the chapter on group selection - to ESS theory. Kin selection is also here, as a form of group selection! Evidently Wilson's weird infatuation with "group selection" goes way back: unfortunate in a biologist who is so justly influential."

      so, does ESS better explain group phenomena? does this allow us to retain the gene as currency and acknowledge group cooperation?

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