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本文引用的文献

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A COMPARISON OF GENETIC AND PHENOTYPIC CORRELATIONS.遗传相关性与表型相关性的比较
Evolution. 1988 Sep;42(5):958-968. doi: 10.1111/j.1558-5646.1988.tb02514.x.
2
QUANTITATIVE GENETIC ANALYSIS OF MULTIVARIATE EVOLUTION, APPLIED TO BRAIN:BODY SIZE ALLOMETRY.多变量进化的定量遗传分析,应用于脑体大小异速生长
Evolution. 1979 Mar;33(1Part2):402-416. doi: 10.1111/j.1558-5646.1979.tb04694.x.
3
PHENOTYPIC, GENETIC, AND ENVIRONMENTAL MORPHOLOGICAL INTEGRATION IN THE CRANIUM.颅骨的表型、遗传和环境形态整合
Evolution. 1982 May;36(3):499-516. doi: 10.1111/j.1558-5646.1982.tb05070.x.
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THE MEASUREMENT OF SELECTION ON CORRELATED CHARACTERS.对相关性状选择的度量
Evolution. 1983 Nov;37(6):1210-1226. doi: 10.1111/j.1558-5646.1983.tb00236.x.
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Meta-analysis of magnitudes, differences and variation in evolutionary parameters.进化参数的大小、差异和变异的荟萃分析。
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Evolutionary modeling and correcting for observation error support a 3/5 brain-body allometry for primates.进化建模以及对观测误差的校正支持灵长类动物脑体异速生长的3/5规律。
J Hum Evol. 2016 May;94:106-16. doi: 10.1016/j.jhevol.2016.03.001. Epub 2016 Apr 19.
7
Estimating sampling error of evolutionary statistics based on genetic covariance matrices using maximum likelihood.基于遗传协方差矩阵使用最大似然法估计进化统计学的抽样误差。
J Evol Biol. 2015 Aug;28(8):1542-9. doi: 10.1111/jeb.12674. Epub 2015 Jul 21.
8
Rate of evolutionary change in cranial morphology of the marsupial genus Monodelphis is constrained by the availability of additive genetic variation.有袋类动物单孔目负鼠属颅骨形态的进化变化速率受到加性遗传变异可用性的限制。
J Evol Biol. 2015 Apr;28(4):973-85. doi: 10.1111/jeb.12628. Epub 2015 Apr 17.
9
The macroevolutionary consequences of phenotypic integration: from development to deep time.表型整合的宏观进化后果:从发育到漫长时间尺度
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10
Assessing trait covariation and morphological integration on phylogenies using evolutionary covariance matrices.使用进化协方差矩阵评估系统发育树上的性状协变和形态整合。
PLoS One. 2014 Apr 11;9(4):e94335. doi: 10.1371/journal.pone.0094335. eCollection 2014.

还需要多少?形态整合与进化能力研究中的样本量确定

How many more? Sample size determination in studies of morphological integration and evolvability.

作者信息

Grabowski Mark, Porto Arthur

机构信息

Division of Anthropology, American Museum of Natural History, New York, 10024.

Centre for Ecological and Evolutionary Synthesis (CEES), Department of Biosciences, University of Oslo, 0316 Oslo, Norway.

出版信息

Methods Ecol Evol. 2017 May;8(5):592-603. doi: 10.1111/2041-210X.12674. Epub 2016 Nov 7.

DOI:10.1111/2041-210X.12674
PMID:28503291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5423670/
Abstract
  1. The variational properties of living organisms are an important component of current evolutionary theory. As a consequence, researchers working on the field of multivariate evolution have increasingly used integration and evolvability statistics as a way of capturing the potentially complex patterns of trait association and their effects over evolutionary trajectories. Little attention has been paid, however, to the cascading effects that inaccurate estimates of trait covariance have on these widely used evolutionary statistics. 2. Here, we analyze the relationship between sampling effort and inaccuracy in evolvability and integration statistics calculated from 10-trait matrices with varying patterns of covariation and magnitudes of integration. We then extrapolate our initial approach to different numbers of traits and different magnitudes of integration and estimate general equations relating the inaccuracy of the statistics of interest to sampling effort. We validate our equations using a dataset of cranial traits, and use them to make sample size recommendations. 3. Our results suggest that highly inaccurate estimates of evolvability and integration statistics resulting from small sample sizes are likely common in the literature, given the sampling effort necessary to properly estimate them. We also show that patterns of covariation have no effect on the sampling properties of these statistics, but overall magnitudes of integration interact with sample size and lead to varying degrees of bias, imprecision, and inaccuracy. 4. Finally, we provide R functions that can be used to calculate recommended sample sizes or to simply estimate the level of inaccuracy that should be expected in these statistics, given a sampling design.
摘要
  1. 生物体的变异性是当前进化理论的一个重要组成部分。因此,从事多变量进化领域研究的人员越来越多地使用整合和可进化性统计数据,以此来捕捉性状关联的潜在复杂模式及其对进化轨迹的影响。然而,性状协方差的不准确估计对这些广泛使用的进化统计数据所产生的级联效应却很少受到关注。2. 在这里,我们分析了采样量与根据具有不同协变模式和整合量的10个性状矩阵计算出的可进化性和整合统计数据中的不准确性之间的关系。然后,我们将最初的方法推广到不同数量的性状和不同的整合量,并估计出将感兴趣的统计数据的不准确性与采样量相关联的通用方程。我们使用一个颅骨性状数据集验证了我们的方程,并利用它们给出样本量建议。3. 我们的结果表明,鉴于准确估计所需的采样量,文献中因样本量小而导致的可进化性和整合统计数据的高度不准确估计可能很常见。我们还表明,协变模式对这些统计数据的采样特性没有影响,但整合的总体量与样本量相互作用,会导致不同程度的偏差、不精确性和不准确性。4. 最后,我们提供了R函数,这些函数可用于计算推荐的样本量,或者在给定采样设计的情况下,简单地估计这些统计数据中预期的不准确性水平。