Institut de Biologie, École Normale Supérieure, 75005 Paris, France; Graduate Program in Organismic and Evolutionary Biology, University of Massachusetts Amherst, Amherst, MA 01003, USA; Department of Integrative Biology, Oklahoma State University, Stillwater, OK 74078, USA;
Institut de Biologie, École Normale Supérieure, 75005 Paris, France;
Syst Biol. 2016 Jan;65(1):146-60. doi: 10.1093/sysbio/syv073. Epub 2015 Oct 9.
Striking evolutionary convergence can lead to similar sets of species in different locations, such as in cichlid fishes and Anolis lizards, and suggests that evolution can be repeatable and predictable across clades. Yet, most examples of convergence involve relatively small temporal and/or spatial scales. Some authors have speculated that at larger scales (e.g., across continents), differing evolutionary histories will prevent convergence. However, few studies have compared the contrasting roles of convergence and history, and none have done so at large scales. Here we develop a two-part approach to test the scale over which convergence can occur, comparing the relative importance of convergence and history in macroevolution using phylogenetic models of adaptive evolution. We apply this approach to data from morphology, ecology, and phylogeny from 167 species of anuran amphibians (frogs) from 10 local sites across the world, spanning ~160 myr of evolution. Mapping ecology on the phylogeny revealed that similar microhabitat specialists (e.g., aquatic, arboreal) have evolved repeatedly across clades and regions, producing many evolutionary replicates for testing for morphological convergence. By comparing morphological optima for clades and microhabitat types (our first test), we find that convergence associated with microhabitat use dominates frog morphological evolution, producing recurrent ecomorphs that together encompass all sampled species in each community in each region. However, our second test, which examines whether and how much species differ from their inferred optima, shows that convergence is incomplete: that is, phenotypes of most species are still somewhat distant from the estimated optimum for each microhabitat, seemingly because of insufficient time for more complete adaptation (an effect of history). Yet, these effects of history are related to past ecologies, and not clade membership. Overall, our study elucidates the dominant drivers of morphological evolution across a major vertebrate clade and shows that evolution can be repeatable at much greater temporal and spatial scales than commonly thought. It also provides an analytical framework for testing other potential examples of large-scale convergence.
显著的进化趋同会导致不同地理位置出现相似的物种集合,例如在慈鲷鱼和变色蜥蜴中,这表明进化在不同的进化枝中是可重复和可预测的。然而,大多数趋同的例子涉及相对较小的时间和/或空间尺度。一些作者推测,在更大的尺度上(例如,跨越大陆),不同的进化历史将阻止趋同。然而,很少有研究比较趋同和历史的对比作用,也没有在大尺度上进行这样的研究。在这里,我们开发了一种两部分的方法来测试趋同发生的规模,使用适应性进化的系统发育模型来比较趋同和历史在宏观进化中的相对重要性。我们将这种方法应用于来自全球 10 个地点的 167 种蛙类(青蛙)的形态学、生态学和系统发育数据,跨越了约 1.6 亿年的进化。在系统发育树上映射生态学揭示了相似的微生境特化(例如,水生、树栖)在进化枝和区域中反复进化,为测试形态趋同提供了许多进化重复。通过比较类群和微生境类型的形态最优值(我们的第一个测试),我们发现与微生境利用相关的趋同主导着青蛙的形态进化,产生了反复出现的生态型,共同包含了每个区域每个群落中所有采样的物种。然而,我们的第二个测试,即检查物种是否以及在多大程度上与其推断的最优值不同,表明趋同是不完全的:也就是说,大多数物种的表型仍然与每个微生境的估计最优值有些距离,似乎是因为适应时间不够充分(历史的影响)。然而,这些历史效应与过去的生态有关,而与进化枝成员无关。总的来说,我们的研究阐明了主要脊椎动物进化枝中形态进化的主要驱动因素,并表明进化在比通常认为的更大的时间和空间尺度上是可重复的。它还为测试其他潜在的大尺度趋同的例子提供了一个分析框架。