Pub Date : 2022-03-21DOI: 10.1007/s11692-022-09567-z
J. DiFrisco, G. Wagner
{"title":"Body Plan Identity: A Mechanistic Model","authors":"J. DiFrisco, G. Wagner","doi":"10.1007/s11692-022-09567-z","DOIUrl":"https://doi.org/10.1007/s11692-022-09567-z","url":null,"abstract":"","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"49 1","pages":"123 - 141"},"PeriodicalIF":2.5,"publicationDate":"2022-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47921565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-18DOI: 10.1007/s11692-022-09562-4
Gavin Stark, D. Pincheira‐Donoso
{"title":"The Evolution of Brain Size in Ectothermic Tetrapods: Large Brain Mass Trades-Off with Lifespan in Reptiles","authors":"Gavin Stark, D. Pincheira‐Donoso","doi":"10.1007/s11692-022-09562-4","DOIUrl":"https://doi.org/10.1007/s11692-022-09562-4","url":null,"abstract":"","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"49 1","pages":"180 - 188"},"PeriodicalIF":2.5,"publicationDate":"2022-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43285950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-16DOI: 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.
{"title":"Procrustes Shape Cannot be Analyzed, Interpreted or Visualized one Landmark at a Time","authors":"Andrea Cardini, Verderame Adolfo Marco","doi":"10.1007/s11692-022-09565-1","DOIUrl":"https://doi.org/10.1007/s11692-022-09565-1","url":null,"abstract":"<p>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.</p>","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"12 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2022-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138532902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-01DOI: 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.
{"title":"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","authors":"Gregory S. Paul, W. Scott Persons, Jay Van Raalte","doi":"10.1007/s11692-022-09561-5","DOIUrl":"https://doi.org/10.1007/s11692-022-09561-5","url":null,"abstract":"<p>All skeletal specimens of the North American dinosaur <i>Tyrannosaurus</i> and a number of trace fossils have been attributed to the single species: <i>T. rex</i>. 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 <i>Tyrannosaurus</i> 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 <i>Tyrannosaurus</i> 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 <i>Tyrannosaurus</i> 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 <i>Tyrannosaurus</i> species are examined. A discussion of the issues involving the recognition and designation of multiple morphotypes/species within dinosaur genera is included.</p>","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"1 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138532948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-21DOI: 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 (Δz̅ = Gβ), a multivariate expansion of the breeder’s equation, where phenotypic change (Δz̅) 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.
{"title":"Comparative Quantitative Genetics of the Pelvis in Four-Species of Rodents and the Conservation of Genetic Covariance and Correlation Structure","authors":"Carl J. Saltzberg, Laura I. Walker, Lee E. Chipps-Walton, Bárbara M. A. Costa, Ángel E. Spotorno, Scott J. Steppan","doi":"10.1007/s11692-022-09559-z","DOIUrl":"https://doi.org/10.1007/s11692-022-09559-z","url":null,"abstract":"<p>Quantitative genetics is a powerful tool for predicting phenotypic evolution on a microevolutionary scale. This predictive power primarily comes from the Lande equation (Δ<b>z̅</b> = <b>Gβ</b>), a multivariate expansion of the breeder’s equation, where phenotypic change (Δ<b>z̅</b>) is predicted from the genetic covariances (<b>G</b>) and selection (<b>β</b>). 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 <b>G</b>-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 <i>Phyllotis vaccarum</i> and <i>P. darwini</i> and estimated the <b>G</b>-matrices for eight pelvic traits. To expand our phylogenetic breadth, we incorporated two additional <b>G</b>-matrices measured for the same traits from Kohn & Atchley’s 1988 study of the murine rodents <i>Mus musculus</i> and <i>Rattus norvegicus</i>. Using a phylogenetic comparative framework and four separate metrics of matrix divergence or similarity, we found no significant association between evolutionary divergence among species <b>G</b>-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.</p>","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"10 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2022-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138532901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-14DOI: 10.1007/s11692-022-09560-6
G. Markevich, E. I. Izvekova, L. Anisimova, N. Mugue, T. V. Bonk, E. Esin
{"title":"Annual Temperatures and Dynamics of Food Availability are Associated with the Pelagic-Benthic Diversification in a Sympatric Pair of Salmonid Fish","authors":"G. Markevich, E. I. Izvekova, L. Anisimova, N. Mugue, T. V. Bonk, E. Esin","doi":"10.1007/s11692-022-09560-6","DOIUrl":"https://doi.org/10.1007/s11692-022-09560-6","url":null,"abstract":"","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"1 1","pages":"1-14"},"PeriodicalIF":2.5,"publicationDate":"2022-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41568245","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-09DOI: 10.1007/s11692-022-09563-3
F. Shkil, V. Borisov, Dmitry Seleznev, D. Kapitanova, B. Abdissa, K. Dzerzhinskii, S. Smirnov
{"title":"Intra- and interspecific variability of the cranial ossification sequences in Barbus sensu lato.","authors":"F. Shkil, V. Borisov, Dmitry Seleznev, D. Kapitanova, B. Abdissa, K. Dzerzhinskii, S. Smirnov","doi":"10.1007/s11692-022-09563-3","DOIUrl":"https://doi.org/10.1007/s11692-022-09563-3","url":null,"abstract":"","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"49 1","pages":"189 - 204"},"PeriodicalIF":2.5,"publicationDate":"2022-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47423449","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-01-24DOI: 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.
{"title":"ES-sim-GLM, a Multiple Regression Trait-Dependent Diversification Approach","authors":"Matthew O. Moreira, Carlos Fonseca, Danny Rojas","doi":"10.1007/s11692-021-09557-7","DOIUrl":"https://doi.org/10.1007/s11692-021-09557-7","url":null,"abstract":"<p>Identifying the role of quantitative variables on speciation rates is among the main purposes of trait-dependent diversification methods. <i>ES-sim</i>, 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 <i>ES-sim</i> and integrated generalized linear models instead of Pearson’s correlations. We named the new approach as <i>ES-sim</i>-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, <i>ES-sim</i>-GLM for single regression models shows high power, low false discovery rates and is robust to incomplete taxon sampling. <i>ES-sim</i>-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.</p>","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"2 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2022-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138532947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-01-12DOI: 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.
{"title":"Evolutionary Processes in Cancer","authors":"","doi":"10.1093/obo/9780199941728-0139","DOIUrl":"https://doi.org/10.1093/obo/9780199941728-0139","url":null,"abstract":"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.","PeriodicalId":50471,"journal":{"name":"Evolutionary Biology","volume":"1 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2022-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44643363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}