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Body Plan Identity: A Mechanistic Model 身体计划同一性:一个机制模型
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-03-21 DOI: 10.1007/s11692-022-09567-z
J. DiFrisco, G. Wagner
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引用次数: 8
The Evolution of Brain Size in Ectothermic Tetrapods: Large Brain Mass Trades-Off with Lifespan in Reptiles 变温四足动物脑容量的进化:爬行动物脑容量大与寿命的交换
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-03-18 DOI: 10.1007/s11692-022-09562-4
Gavin Stark, D. Pincheira‐Donoso
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引用次数: 2
Procrustes Shape Cannot be Analyzed, Interpreted or Visualized one Landmark at a Time Procrustes的形状不能一次分析、解释或可视化一个地标
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-03-16 DOI: 10.1007/s11692-022-09565-1
Andrea Cardini, Verderame Adolfo Marco

Landmark-based geometric morphometrics using the Procrustes approach has become the dominant family of methods in morphometrics. However, the superimposition (and sliding, if semilandmarks are present), that transforms raw coordinates into shape coordinates is biologically arbitrary. Procrustes has desirable statistical properties, but is not based on a biological model. The same is true for sliding methods. These techniques allow powerful statistical analyses of a full set of shape coordinates, but make the use of subsets of landmarks/semilandmarks problematic, inaccurate and misleading, if not totally wrong. Crucially, the biological arbitrariness of the superimposition prevents any meaningful quantification, analysis and interpretation of variation one landmark/semilandmark at a time. We exemplify how misleading this type of analyses can be by using a real dataset, as well as simulated data with isotropic variation. Both show inconsistencies in ‘per-landmark/semilandmark’ variances. The simulation in fact helps to make even more obvious that the pattern of variance is strongly influenced by the biologically arbitrary choice of the mathematical treatment. Unfortunately, despite this limitation of all superimposition methods being known since the early days of Procrustean morphometrics, there has been a recent series of papers in leading journals presenting results of ‘per-landmark’ analyses. Thus, we further clarify why these analyses are wrong and represent misleading examples that should not be followed: Procrustes shape data cannot be analyzed, visualized or interpreted one landmark at a time. For users who are in doubt, in the Conclusions, we provide a short list of recommendations on how to easily avoid this type of mistakes.

使用Procrustes方法的基于地标的几何形态测量学已经成为形态测量学中占主导地位的方法。然而,将原始坐标转换为形状坐标的叠加(以及滑动,如果存在半标记)在生物学上是任意的。Procrustes具有理想的统计特性,但不是基于生物学模型。滑动方法也是如此。这些技术允许对完整的形状坐标集进行强大的统计分析,但使地标/半地标子集的使用成为问题,不准确和误导,如果不是完全错误的话。至关重要的是,叠加的生物任意性阻止了对一个里程碑/半里程碑的变化进行任何有意义的量化、分析和解释。我们通过使用真实数据集以及具有各向同性变化的模拟数据来举例说明这种类型的分析是如何误导的。两者在“每里程碑/半里程碑”差异上都表现出不一致。事实上,模拟有助于更明显地表明,方差的模式受到数学处理的生物学任意选择的强烈影响。不幸的是,尽管自Procrustean形态计量学早期以来已知的所有叠加方法都存在这种局限性,但最近在主要期刊上发表了一系列论文,介绍了“每个里程碑”分析的结果。因此,我们进一步澄清了为什么这些分析是错误的,并代表了不应该遵循的误导性示例:Procrustes形状数据不能一次分析,可视化或解释一个地标。对于有疑问的用户,在结论中,我们提供了一个简短的建议列表,说明如何轻松避免这类错误。
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引用次数: 0
The Tyrant Lizard King, Queen and Emperor: Multiple Lines of Morphological and Stratigraphic Evidence Support Subtle Evolution and Probable Speciation Within the North American Genus Tyrannosaurus 暴君蜥蜴国王、王后和皇帝:多条形态学和地层证据支持北美暴龙属的微妙进化和可能的物种形成
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-03-01 DOI: 10.1007/s11692-022-09561-5
Gregory S. Paul, W. Scott Persons, Jay Van Raalte

All skeletal specimens of the North American dinosaur Tyrannosaurus and a number of trace fossils have been attributed to the single species: T. rex. Although an unusual degree of variation in skeletal robustness among specimens and variability in anterior dentary tooth form have been noted, the possibility of sibling species within the genus Tyrannosaurus has never been tested in depth in both anatomical and stratigraphic terms. New analysis, based on a dataset of over three dozen specimens, finds that Tyrannosaurus specimens exhibit such a remarkable degree of proportional variations, distributed at different stratigraphic levels, that the pattern favors multiple species at least partly separated by time; ontogenetic and sexual causes being less consistent with the data. Variation in dentary incisiform counts correlate with skeletal robusticity and also appear to change over time. Based on the current evidence, three morphotypes are demonstrated, and two additional species of Tyrannosaurus are diagnosed and named. One robust species with two small incisors in each dentary appears to have been present initially, followed by two contemporaneous species (one robust and another gracile) both of which had one small incisor in each dentary, suggesting both anagenesis and cladogenesis occurred. The geological/geographic forces underlying the evolution of multiple Tyrannosaurus species are examined. A discussion of the issues involving the recognition and designation of multiple morphotypes/species within dinosaur genera is included.

所有北美恐龙暴龙的骨骼标本和一些化石痕迹都被归为单一物种:霸王龙。尽管已经注意到标本之间骨骼健壮性的不同寻常程度的差异和前齿状牙齿形式的差异,但在暴龙属中兄弟物种的可能性从未在解剖学和地层学方面进行过深入的测试。新的分析基于超过36个标本的数据集,发现暴龙标本呈现出如此显著的比例变化,分布在不同的地层水平,这种模式有利于多个物种,至少部分是由时间分开的;个体成因和性原因与数据不太一致。牙齿切形数的变化与骨骼健壮性相关,也随着时间的推移而变化。根据目前的证据,展示了三种形态,并诊断和命名了另外两种暴龙。一种强壮的物种在每根牙齿上都有两个小门牙,随后出现了两个同时期的物种(一个强壮的和另一个纤细的),每根牙齿上都有一个小门牙,这表明发生了发育和枝发生。地质/地理力量的演变背后的多种暴龙物种进行了检查。讨论了恐龙属中多种形态/物种的识别和指定问题。
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引用次数: 5
Comparative Quantitative Genetics of the Pelvis in Four-Species of Rodents and the Conservation of Genetic Covariance and Correlation Structure 四种啮齿类动物骨盆的比较数量遗传学及遗传协方差和相关结构的保存
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-02-21 DOI: 10.1007/s11692-022-09559-z
Carl J. Saltzberg, Laura I. Walker, Lee E. Chipps-Walton, Bárbara M. A. Costa, Ángel E. Spotorno, Scott J. Steppan

Quantitative genetics is a powerful tool for predicting phenotypic evolution on a microevolutionary scale. This predictive power primarily comes from the Lande equation (Δ = ), a multivariate expansion of the breeder’s equation, where phenotypic change (Δ) is predicted from the genetic covariances (G) and selection (β). Typically restricted to generational change, evolutionary biologists have proposed that quantitative genetics could bridge micro- and macroevolutionary patterns if predictions were expanded to longer timescales. While mathematically possible, making quantitative genetic predictions across generations or species is contentiously debated, principally in assuming long-term stability of the G-matrix. Here we tested stability at a macroevolutionary timescale by conducting full- and half-sib breeding programs in two species of sigmodontine rodents from South America, the leaf-eared mice Phyllotis vaccarum and P. darwini and estimated the G-matrices for eight pelvic traits. To expand our phylogenetic breadth, we incorporated two additional G-matrices measured for the same traits from Kohn & Atchley’s 1988 study of the murine rodents Mus musculus and Rattus norvegicus. Using a phylogenetic comparative framework and four separate metrics of matrix divergence or similarity, we found no significant association between evolutionary divergence among species G-matrices and time, supporting the assumption of stability for at least some structures. However, the phylogenetic sample size is necessarily small. We suggest that small fluctuations in covariance structure can occur rapidly, but underlying developmental regulation prevents significant divergence at macroevolutionary scales, analogous to an Ornstein–Uhlenbeck pattern. Expanded taxonomic sampling will be needed to test this suggestion.

数量遗传学是在微观进化尺度上预测表型进化的有力工具。这种预测能力主要来自朗德方程(Δz′s = Gβ),这是育种方程的多变量扩展,其中表型变化(Δz′s)是通过遗传协方差(G)和选择(β)来预测的。进化生物学家提出,如果预测扩展到更长的时间尺度,数量遗传学可以在微观和宏观进化模式之间建立桥梁。虽然在数学上是可能的,但对跨代或跨物种进行定量遗传预测仍存在争议,主要是在假设g矩阵长期稳定的情况下。在这里,我们通过对南美叶耳鼠Phyllotis vaccum和P. darwini进行全同胞和半同胞繁殖计划,测试了在宏观进化时间尺度上的稳定性,并估计了8种骨盆特征的g矩阵。为了扩大我们的系统发育广度,我们结合了两个额外的g矩阵,测量来自Kohn &阿奇利1988年对老鼠啮齿类动物小家鼠和褐家鼠的研究。利用系统发育比较框架和矩阵差异或相似性的四个独立度量,我们发现物种g -矩阵的进化差异与时间之间没有显著关联,这支持了至少某些结构的稳定性假设。然而,系统发育样本量必然很小。我们认为协方差结构的微小波动可以迅速发生,但潜在的发育调节阻止了宏观进化尺度上的显著差异,类似于Ornstein-Uhlenbeck模式。需要扩大分类学抽样来检验这一建议。
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引用次数: 3
Annual Temperatures and Dynamics of Food Availability are Associated with the Pelagic-Benthic Diversification in a Sympatric Pair of Salmonid Fish 年温度和食物供应的动态与同域一对鲑鱼的中上层-底栖多样化有关
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-02-14 DOI: 10.1007/s11692-022-09560-6
G. Markevich, E. I. Izvekova, L. Anisimova, N. Mugue, T. V. Bonk, E. Esin
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引用次数: 1
Intra- and interspecific variability of the cranial ossification sequences in Barbus sensu lato. 猕猴颅骨骨化序列的种内和种间变异。
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-02-09 DOI: 10.1007/s11692-022-09563-3
F. Shkil, V. Borisov, Dmitry Seleznev, D. Kapitanova, B. Abdissa, K. Dzerzhinskii, S. Smirnov
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引用次数: 1
ES-sim-GLM, a Multiple Regression Trait-Dependent Diversification Approach ES-sim-GLM,一种多元回归特征相关多样化方法
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-01-24 DOI: 10.1007/s11692-021-09557-7
Matthew O. Moreira, Carlos Fonseca, Danny Rojas

Identifying the role of quantitative variables on speciation rates is among the main purposes of trait-dependent diversification methods. ES-sim, a recent simulation-based approach that relies on Pearson’s correlations, allows testing trait-dependent diversification for single regression models. Here, we modified this approach to include generalized linear models and two independent variables. To examine the effects of multiple traits on speciation we modified ES-sim and integrated generalized linear models instead of Pearson’s correlations. We named the new approach as ES-sim-GLM. We further evaluated how this modified method performs in both single and multiple regression modelling. For this, we analyzed the relationship of speciation rates with geographic range size and snout-to-vent length in 216 species from the family Liolaemidae, a South American radiation of Andean lizards. Based on simulations, ES-sim-GLM for single regression models shows high power, low false discovery rates and is robust to incomplete taxon sampling. ES-sim-GLM for multiple regression models shows lower power but also low false-discovery rates. Both remained computationally efficient. Using Liolaemidae data, we found that larger species but with smaller species geographic range sizes were associated with higher speciation rates. To the best of our knowledge, no study as addressed these relationships in this clade. Our results provide new insights on macroevolutionary methods that should be relevant to all organisms and facilitate future studies that aim to understand diversification patterns across the Tree of Life.

确定数量变量对物种形成率的作用是性状依赖多样化方法的主要目的之一。ES-sim是最近一种基于模拟的方法,它依赖于Pearson的相关性,允许测试单个回归模型的性状依赖多样化。在这里,我们修改了这种方法,包括广义线性模型和两个自变量。为了研究多性状对物种形成的影响,我们修改了ES-sim模型,并集成了广义线性模型,而不是Pearson相关模型。我们将这种新方法命名为ES-sim-GLM。我们进一步评估了这种改进的方法在单次和多次回归建模中的表现。为此,我们分析了安第斯蜥蜴科216种的物种形成率与地理范围大小和口口长度的关系。仿真结果表明,单回归模型的ES-sim-GLM具有高功率、低错误发现率和对不完全分类群采样的鲁棒性。ES-sim-GLM用于多元回归模型显示出较低的功率,但也较低的错误发现率。两者都保持了计算效率。利用油油虫科的数据,我们发现,较大的物种和较小的物种地理范围大小与较高的物种形成率相关。据我们所知,目前还没有研究涉及这一分支的这些关系。我们的研究结果提供了与所有生物相关的宏观进化方法的新见解,并促进了旨在理解生命之树多样化模式的未来研究。
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引用次数: 0
Evolutionary Processes in Cancer 癌症的进化过程
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-01-12 DOI: 10.1093/obo/9780199941728-0139
Cancer develops through the evolution of somatic cells in multicellular bodies. The familiar dynamics of organismal evolution, including mutations, natural selection, genetic drift, and migration, also occur among the cells of multicellular organisms. In some cases, but not all, these evolutionary processes lead to cancer. This has profound implications for both our understanding of cancer and our treatment of the disease, as well as its prevention. All of our medical interventions impose selective pressures on the heterogeneous populations of billions of cells in tumors, and tend to select for mutant cells that are resistant to the intervention, regardless of whether the intervention is a drug, radiation, the immune system, or anything else that has been tried. We will likely need evolutionary and ecological approaches to cancer to manage its evolution in response to our interventions. The field of the evolutionary biology and ecology of cancer is still young and relatively small. We are in the early stages of translating ideas and tools from evolutionary biology and ecology to study and manage cancers. There is a desperate need for more researchers with expertise in evolutionary biology and ecology to apply their skills and ideas to cancer. Currently, there are far more important questions that need to be addressed than there are people to address them.
癌症是通过多细胞体内体细胞的进化而发展起来的。常见的生物进化动力学,包括突变、自然选择、基因漂移和迁移,也发生在多细胞生物的细胞中。在某些情况下,但不是所有情况下,这些进化过程会导致癌症。这对我们理解癌症、治疗和预防癌症有着深远的影响。我们所有的医疗干预措施都对肿瘤中数十亿细胞的异质性群体施加了选择性压力,并倾向于选择对干预有抵抗力的突变细胞,无论干预是药物、辐射、免疫系统还是任何其他已经尝试过的方法。我们可能需要对癌症采取进化和生态学方法来管理其进化,以应对我们的干预措施。癌症的进化生物学和生态学领域还很年轻,相对较小。我们正处于将进化生物学和生态学的思想和工具转化为研究和管理癌症的早期阶段。迫切需要更多具有进化生物学和生态学专业知识的研究人员将他们的技能和想法应用于癌症。目前,需要解决的重要问题远远多于需要解决的人。
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引用次数: 0
Surface Representation and Morphometric Analysis Based on Discrete Cosine Transform 基于离散余弦变换的曲面表示与形态计量学分析
IF 2.5 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Pub Date : 2022-01-11 DOI: 10.1007/s11692-021-09558-6
Bingjue Li, Shengmin Zhou, Heng Nie
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引用次数: 0
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Evolutionary Biology
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