Laboratory of Evolutionary Biodemography, Max Planck Institute for Demographic Research, Rostock, Germany.
Proc Biol Sci. 2011 Mar 22;278(1707):801-9. doi: 10.1098/rspb.2010.2190. Epub 2010 Dec 1.
The age-specific mortality curve for many species, including humans, is U-shaped: mortality declines with age in the developing cohort (ontogenescence) before increasing with age (senescence). The field of evolutionary demography has long focused on understanding the evolution of senescence while largely failing to address the evolution of ontogenescence. The current review is the first to gather the few available hypotheses addressing the evolution of ontogenescence, examine the basis and assumptions of each and ask what the phylogenetic extent of ontogenescence may be. Ontogenescence is among the most widespread of life-history traits, occurring in every population for which I have found sufficiently detailed data, in major groups throughout the eukaryotes, across many causes of death and many life-history types. Hypotheses seeking to explain ontogenescence include those based on kin selection, the acquisition of robustness, heterogeneous frailties and life-history optimization. I propose a further hypothesis, arguing that mortality drops with age because most transitions that could trigger the risks caused by genetic and developmental malfunctions are concentrated in early life. Of these hypotheses, only those that frame ontogenescence as an evolutionary by-product rather than an adaptation can explain the tremendous diversity of organisms and environments in which it occurs.
包括人类在内的许多物种的特定年龄死亡率曲线呈 U 形:在发育队列(个体发生)中,死亡率随年龄的增长而下降,然后随年龄的增长而增加(衰老)。进化人口学领域长期以来一直专注于理解衰老的进化,而在很大程度上未能解决个体发生的进化。本综述首次收集了少数几个关于个体发生进化的假设,检查了每个假设的依据和假设,并询问了个体发生的系统发生范围可能是什么。个体发生是生命史特征中最广泛的特征之一,在我找到足够详细数据的每个种群中都存在,在真核生物的主要群体中,在许多死亡原因和许多生命史类型中都存在。试图解释个体发生的假说包括基于亲属选择、稳健性获得、异质性脆弱性和生命史优化的假说。我提出了另一个假说,认为死亡率随年龄下降,因为大多数可能引发由遗传和发育故障引起的风险的转变都集中在生命早期。在这些假说中,只有那些将个体发生视为进化副产品而不是适应的假说,才能解释它发生的生物体和环境的巨大多样性。