Ecology and Evolutionary Biology, 443 Hesler, University of Tennessee, Knoxville, Tennessee 37996-1610, USA.
Evolution. 2011 Jul;65(7):1862-78. doi: 10.1111/j.1558-5646.2011.01251.x. Epub 2011 Mar 25.
The absence of an adequate fossil record can hinder understanding the process of diversification that underlies the evolutionary history of a given group. In such cases, investigators have used ultrametric trees derived from molecular data from extant taxa to gain insights into processes of speciation and extinction over time. Inadequate taxon sampling, however, impairs such inferences. In this study, we use simulations to investigate the effect of incomplete taxon sampling on the accumulation of lineages through time for a clade of mushroom-forming fungi, the Hebelomateae. To achieve complete taxon sampling, we use a new Bayesian approach that incorporates substitute lineages to estimate diversification rates. Unlike many studies of animals and plants, we find no evidence of a slowdown in speciation. This indicates the Hebelomateae has not undergone an adaptive radiation. Rather, these fungi have evolved under a relatively constant rate of diversification since their most recent common ancestor, which we date back to the Eocene. The estimated net diversification rate (0.08-0.19 spp./lineage/Ma) is comparable with that of many plants and animals. We suggest that continuous diversification in the Hebelomateae has been facilitated by climatic and vegetation changes throughout the Cenozoic. We also caution against modeling multiple genes as a single partition when performing phylogenetic dating analyses.
化石记录的缺失可能会阻碍人们理解特定群体进化历史背后的多样化过程。在这种情况下,研究人员使用来自现存分类单元的分子数据得出的超支树,来深入了解随时间推移的物种形成和灭绝过程。然而,分类单元取样不足会影响此类推断。在这项研究中,我们使用模拟来研究不完全分类单元取样对蘑菇形成真菌 Hebelomateae 类群随时间积累谱系的影响。为了实现完全的分类单元取样,我们使用一种新的贝叶斯方法,该方法结合了替代谱系来估计多样化率。与许多动物和植物的研究不同,我们没有发现物种形成速度放缓的证据。这表明 Hebelomateae 没有经历过适应性辐射。相反,这些真菌自最近的共同祖先以来一直在以相对稳定的多样化速率进化,我们将其追溯到始新世。估计的净多样化率(0.08-0.19 spp./谱系/百万年)与许多植物和动物相当。我们认为,整个新生代气候和植被的变化促进了 Hebelomateae 的持续多样化。我们还提醒人们在进行系统发育年代测定分析时,不要将多个基因建模为单个分区。