少点错误 2024年09月28日
Thoughts on Evo-Bio Math and Mesa-Optimization: Maybe We Need To Think Harder About "Relative" Fitness?
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文章探讨自然选择是否依据包含性相对生殖适应度,性选择是否更有可能如此,还提到了生物学家对自然选择的看法以及相关争议。

🌐自然选择在一般情况下,其选择的生殖适应度类型并非相对的。地球DNA的最粗略分母,即'底线'总体复制率,并非绝对上限,且人类世可能使其迅速增加,但从长远看,进化产生人类可能最终使DNA毁灭。

🦘当地总体DNA复制率,无论是整个生物圈、鼬科动物的进化枝,还是后院构成的生态系统,实际上都受到环境中资源对这些生物体可用性的限制。自然选择对基因环境方面的塑造,在每个局部情况下,取决于每种'对抗性'适应在多大程度上能略微增加等位基因的最终绝对后代锥体。

💑生物学家普遍认为自然选择在理论上直接优化包含性相对适应度,因为在有性物种中存在一种类似台面优化守护进程的东西在起作用。作者认为将'包含性相对生殖适应度'作为性选择的特定优化目标,可能会开启一个潜在有益的研究领域。

Published on September 28, 2024 2:07 PM GMT

Does natural selection, in general, really go by inclusive relative reproductive fitness?

Does sexual selection? This seems somewhat likelier.

Obviously there's a trivial sense in which the type of reproductive fitness that natural selection selects for, in general, is not relative. The coarsest denominator, the "bottom-line" aggregate replication rate of DNA-on-Earth, isn't capped as an absolute, and I imagine [although I could be wrong about this?] that the Anthropocene has rapidly increased it [even as "Evolution, in producing humans, may have entirely doomed DNA" in the long run].

Instead, local aggregate DNA replication rates - whether of the entire biosphere, of the clade Mustelidae, or of the ecosystem constituted by your backyard - are capped in practice by the availability of resources-in-the-environment to those organisms. The extent to which natural selection is modeling aspects of the gene's environment - prey species, predator species, resource-competing species, members of its own species - as adversaries, will of course in the most abstract theory of "what natural selection is" depend, in each local case, on how much each "adversarial" adaptation can marginally be expected to increase the allele's ultimate absolute descendants-cone.

I think biologists have come to think of natural selection, in general, as optimizing - even in theory - directly for inclusive relative fitness, because something like a mesa-optimization daemon which actually does do this even-in-theory, is operating in sexual species - a set-of-conditions for the gene/allele where all aspects of "maximize my descendants-cone" that are not "maximize my share of the species's descendants-cone [which species's replication rate is, from the gene's-eye, abstracted-away as invariant]" are functionally ignored by the main logical engine of mutation.

Biologists and those generally familiar with evo-bio math - I predict - will object to my suggestion that we reframe "inclusive relative reproductive fitness" as an optimization target of sexual selection specifically, on the grounds that it is trivial - of course, since relative fitness as conventionally taken-for-granted - the particular "selfish gene" that implicitly takes its main grounds of likely advancement, as victory in sexual competition with conspecifics - is a sexual-reproduction-confined optimization target, well, biologists already implicitly know not to model asexual cases as optimizing toward that conventionally-understood "relative fitness".

But I think treating this as a mere terminological nitpick, misses a potentially fruitful area of investigation for the question of why sexual reproduction took over at all, threatens to cloud our thinking on this topic in general, and also misses a potential invaluable second non-artificial data point for mesa-optimizer theory [ that is, we might get "natural selection -> sexual selection" AND "sexual selection -> human values", rather than just "natural selection -> human values" ].



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自然选择 性选择 生殖适应度 生物学家
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