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为什么会有如此众多的昆虫物种?来自化石和系统发育学的观点。

Why are there so many insect species? Perspectives from fossils and phylogenies.

作者信息

Mayhew Peter J

机构信息

Department of Biology (Area 18), University of York, PO Box 373, York, YO10 5YW, UK.

出版信息

Biol Rev Camb Philos Soc. 2007 Aug;82(3):425-54. doi: 10.1111/j.1469-185X.2007.00018.x.

Abstract

Over half of all described species are insects, but until recently our understanding of the reasons for this diversity was based on very little macroevolutionary evidence. Here I summarize the hypotheses that have been posed, tests of these hypotheses and their results, and hence identify gaps in knowledge for future researchers to pursue. I focus on inferences from the following sources: (i) the fossil record, normally at family level, and (ii) insect phylogenies, sometimes combined with: (iii) the species richness of insect higher taxa, and (iv) current extinction risks. There is evidence that the species richness of insects has been enhanced by: (i) their relative age, giving time for diversification to take place; (ii) low extinction rates. There is little evidence that rates of origination have generally been high or that there are limits on numbers of species. However, the evidence on macroevolutionary rates is not yet so extensive or coherent as to present unequivocal messages. As regards morphological, ecological, or behavioural hypotheses, there is evidence that diversity has been enhanced by (iii) flight or properties resulting from it like enhanced dispersal, (iv) wing folding, and (v) complete metamorphosis. However, in all these cases the evidence is somewhat equivocal, either because of statistical issues or because evidence from different sources is conflicting. There is extensive evidence that diversity is affected by (vi) the ecological niche. Comparative studies indicate that phytophagy generally increases net diversification rates, and reduces extinction risk. However, niche specialization is also associated with an increase in extinction risk. Small body size (vii) is often associated with low extinction risk in comparative studies, but as yet there is no solid evidence that it consistently enhances net rates of diversification. Mouthpart diversity (viii) has generally increased over time in the insects, but cannot explain the apparent great increase in diversity seen in the Cretaceous and Tertiary. Sexual selection and sexual conflict (ix) are two processes that are widespread in insects, and there is comparative evidence linking both to increased diversification. Although some comparative evidence links tropical distributions (x) to increased rates of diversification, the extent to which latitudinal richness gradients are unusual in insects is equivocal. There is little to no direct evidence from fossils and phylogenies that insect diversity has generally been affected by (i) sensory- or neuro-sophistication, (ii) population size or density, (iii) generation time or fecundity, (iv) the presence of an exoskeleton or cuticle, (v) segmentation or appendage diversity, (vi) adaptability or genetic versatility, though all of these remain plausible hypotheses awaiting further tests. The data suggest that the insect body ground plan itself had no direct effect on insect diversity. Thus, whilst studies to date have given substantial understanding, substantial gaps still remain. Future challenges include: (i) interpreting conflicting messages from different sources of data; (ii) rating the importance of different hypotheses that are statistically supported; (iii) linking specific proximate to specific ultimate explanations and vice versa; and (iv) understanding how different ultimate hypotheses might be dependent on each other.

摘要

已描述的物种中有超过一半是昆虫,但直到最近,我们对这种多样性原因的理解还基于极少的宏观进化证据。在此,我总结已提出的假说、对这些假说的检验及其结果,从而找出知识空白以供未来研究者探索。我重点关注来自以下方面的推断:(i)化石记录,通常为科级水平;(ii)昆虫系统发育,有时会结合:(iii)昆虫高级分类单元的物种丰富度;以及(iv)当前的灭绝风险。有证据表明,昆虫的物种丰富度因以下因素而增加:(i)它们相对古老的年代,这为物种分化提供了时间;(ii)低灭绝率。几乎没有证据表明物种形成速率总体上一直很高,或者物种数量存在限制。然而,关于宏观进化速率的证据尚未广泛到或连贯到能给出明确无误的信息。至于形态学、生态学或行为学假说,有证据表明多样性因以下因素而增加:(iii)飞行或由此产生的特性,如增强的扩散能力;(iv)翅折叠;以及(v)完全变态。然而,在所有这些情况下,证据都有些模棱两可,要么是由于统计问题,要么是因为来自不同来源的证据相互矛盾。有大量证据表明多样性受(vi)生态位影响。比较研究表明,植食性通常会提高净分化速率,并降低灭绝风险。然而,生态位特化也与灭绝风险增加相关。在比较研究中,小体型(vii)通常与低灭绝风险相关,但目前尚无确凿证据表明它能持续提高净分化速率。昆虫口器的多样性(viii)总体上随时间增加,但无法解释在白垩纪和第三纪明显出现的多样性大幅增加。性选择和性冲突(ix)是昆虫中广泛存在的两个过程,有比较证据表明它们都与分化增加有关。尽管一些比较证据将热带分布(x)与分化速率增加联系起来,但昆虫的纬度丰富度梯度有多不寻常还不明确。从化石和系统发育中几乎没有直接证据表明昆虫多样性总体上受到以下因素影响:(i)感官或神经复杂性;(ii)种群大小或密度;(iii)世代时间或繁殖力;(iv)外骨骼或角质层的存在;(v)体节或附肢多样性;(vi)适应性或遗传多样性,尽管所有这些仍然是有待进一步检验的合理假说。数据表明昆虫的身体基本结构本身对昆虫多样性没有直接影响。因此,虽然迄今为止的研究已经有了相当多的认识,但仍然存在很大差距。未来的挑战包括:(i)解读来自不同数据来源的相互矛盾的信息;(ii)评估得到统计支持的不同假说的重要性;(iii)将具体的近因解释与具体的终极解释联系起来,反之亦然;以及(iv)理解不同的终极假说可能如何相互依赖。

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