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The Inappropriate Symmetries of Multivariate Statistical Analysis in Geometric Morphometrics

机译:几何形态计量学中多元统计分析的不适当对称性

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摘要

In today’s geometric morphometrics the commonest multivariate statistical procedures, such as principal component analysis or regressions of Procrustes shape coordinates on Centroid Size, embody a tacit roster of symmetries—axioms concerning the homogeneity of the multiple spatial domains or descriptor vectors involved—that do not correspond to actual biological fact. These techniques are hence inappropriate for any application regarding which we have a-priori biological knowledge to the contrary (e.g., genetic/morphogenetic processes common to multiple landmarks, the range of normal in anatomy atlases, the consequences of growth or function for form). But nearly every morphometric investigation is motivated by prior insights of this sort. We therefore need new tools that explicitly incorporate these elements of knowledge, should they be quantitative, to break the symmetries of the classic morphometric approaches. Some of these are already available in our literature but deserve to be known more widely: deflated (spatially adaptive) reference distributions of Procrustes coordinates, Sewall Wright’s century-old variant of factor analysis, the geometric algebra of importing explicit biomechanical formulas into Procrustes space. Other methods, not yet fully formulated, might involve parameterized models for strain in idealized forms under load, principled approaches to the separation of functional from Brownian aspects of shape variation over time, and, in general, a better understanding of how the formalism of landmarks interacts with the many other approaches to quantification of anatomy. To more powerfully organize inferences from the high-dimensional measurements that characterize so much of today’s organismal biology, tomorrow’s toolkit must rely neither on principal component analysis nor on the Procrustes distance formula, but instead on sound prior biological knowledge as expressed in formulas whose coefficients are not all the same. I describe the problems of the standard techniques, discuss several examples of the alternatives, and draw some conclusions.
机译:在当今的几何形态计量学中,最常见的多元统计程序(例如主成分分析或质心尺寸上的Procrustes形状坐标的回归)体现了默认的对称表(涉及多个空间域或所描述向量的同质性的轴心),不对应到实际的生物学事实。因此,这些技术不适用于我们具有先验生物学知识的任何应用(例如,多个界标共有的遗传/形态发生过程,解剖学图谱的正常范围,生长或形态功能的后果)。但是,几乎所有形态计量学研究都是出于这种先验见解。因此,我们需要新的工具来明确地包含这些知识元素(如果它们是定量的),以打破经典形态计量学方法的对称性。其中一些已经在我们的文献中获得了,但应该得到更广泛的了解:Procrustes坐标的缩小(空间自适应)参考分布,Sewall Wright百年历史的因子分析变体,将明确的生物力学公式导入Procrustes空间的几何代数。其他尚未完全制定的方法可能涉及载荷下理想形式的应变的参数化模型,将函数与形状随时间变化的布朗方面进行分离的原则方法,以及通常更好地理解地标形式化的方式与许多其他用于解剖定量的方法相互作用。为了更有效地组织表征当今许多生物生物学特征的高维测量的推论,明天的工具包必须既不依赖主成分分析也不依赖Procrustes距离公式,而必须依赖系数为并非都一样。我描述了标准技术的问题,讨论了几种替代方法的示例,并得出了一些结论。

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