Gawain T. Antell, Roger B. J. Benson, Erin E. Saupe
The fossil record is spatiotemporally heterogeneous: taxon occurrence data have patchy spatial distributions, and this patchiness varies through time. Large-scale quantitative paleobiology studies that fail to account for heterogeneous sampling coverage will generate uninformative inferences at best and confidently draw wrong conclusions at worst. Explicitly spatial methods of standardization are necessary for analyses of large-scale fossil datasets, because nonspatial sample standardization, such as diversity rarefaction, is insufficient to reduce the signal of varying spatial coverage through time or between environments and clades. Spatial standardization should control both geographic area and dispersion (spread) of fossil localities. In addition to standardizing the spatial distribution of data, other factors may be standardized, including environmental heterogeneity or the number of publications or field collecting units that report taxon occurrences. Using a case study of published global Paleobiology Database occurrences, we demonstrate strong signals of sampling; without spatial standardization, these sampling signatures could be misattributed to biological processes. We discuss practical issues of implementing spatial standardization via subsampling and present the new R package divvy to improve the accessibility of spatial analysis. The software provides three spatial subsampling approaches, as well as related tools to quantify spatial coverage. After reviewing the theory, practice, and history of equalizing spatial coverage between data comparison groups, we outline priority areas to improve related data collection, analysis, and reporting practices in paleobiology.
化石记录具有时空异质性:分类群出现数据的空间分布具有斑块性,这种斑块性随时间而变化。大规模的定量古生物学研究如果没有考虑到取样范围的不均匀性,轻则会得出缺乏信息的推论,重则会得出错误的结论。大规模化石数据集的分析需要明确的空间标准化方法,因为非空间样本标准化(如多样性稀释)不足以减少不同时间或不同环境和支系之间不同空间覆盖的信号。空间标准化既要控制化石地点的地理区域,也要控制化石地点的分散(扩散)。除了对数据的空间分布进行标准化之外,还可以对其他因素进行标准化,包括环境异质性或报告分类群出现的出版物或野外采集单位的数量。通过对已发表的全球古生物数据库中出现的生物进行案例研究,我们展示了强烈的采样信号;如果没有空间标准化,这些采样信号可能会被错误地归因于生物过程。我们讨论了通过子采样实现空间标准化的实际问题,并介绍了新的 R 软件包 divvy,以提高空间分析的可及性。该软件提供了三种空间子取样方法以及量化空间覆盖率的相关工具。在回顾了数据比较组之间空间覆盖率均衡化的理论、实践和历史之后,我们概述了在古生物学中改进相关数据收集、分析和报告实践的优先领域。
{"title":"Spatial standardization of taxon occurrence data—a call to action","authors":"Gawain T. Antell, Roger B. J. Benson, Erin E. Saupe","doi":"10.1017/pab.2023.36","DOIUrl":"https://doi.org/10.1017/pab.2023.36","url":null,"abstract":"<p>The fossil record is spatiotemporally heterogeneous: taxon occurrence data have patchy spatial distributions, and this patchiness varies through time. Large-scale quantitative paleobiology studies that fail to account for heterogeneous sampling coverage will generate uninformative inferences at best and confidently draw wrong conclusions at worst. Explicitly spatial methods of standardization are necessary for analyses of large-scale fossil datasets, because nonspatial sample standardization, such as diversity rarefaction, is insufficient to reduce the signal of varying spatial coverage through time or between environments and clades. Spatial standardization should control both geographic area and dispersion (spread) of fossil localities. In addition to standardizing the spatial distribution of data, other factors may be standardized, including environmental heterogeneity or the number of publications or field collecting units that report taxon occurrences. Using a case study of published global Paleobiology Database occurrences, we demonstrate strong signals of sampling; without spatial standardization, these sampling signatures could be misattributed to biological processes. We discuss practical issues of implementing spatial standardization via subsampling and present the new R package divvy to improve the accessibility of spatial analysis. The software provides three spatial subsampling approaches, as well as related tools to quantify spatial coverage. After reviewing the theory, practice, and history of equalizing spatial coverage between data comparison groups, we outline priority areas to improve related data collection, analysis, and reporting practices in paleobiology.</p>","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"254 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2024-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139690237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The process of evolution and the structures it produces are best understood in the light of hierarchy theory. The biota traditionally is described by either the genealogical Linnaean hierarchy or economic hierarchies of communities or ecosystems. Here we describe the Bretskyan hierarchy—a hybrid eco-genealogical hierarchy that consists of nested sets of different-sized, usually polyphyletic communities of interacting individuals separated from other such communities in space and time at multiple scales. The Bretskyan hierarchy consists of elements that have both genealogical and economic properties and functions—situated between, and connecting the elements of, the economic hierarchies (Vernadskyan) and the genealogical (Linnaean) hierarchy. The described hierarchy at lower tiers is populated by holobionts, individuals composed of multiple polyphyletic lineages integrated by functional interactions or biotically fabricated structures, such as membranes. At larger spatial tiers and longer time scales, the members of the Bretskyan hierarchy are of a more diffuse nature, partially due to the small size and relatively short duration of us as observers of larger and longer-lasting structures, here described as geobiomes. Their individuality is externally forced and directly tied to the spatial and temporal physical structures of our planet. These are sub-bioprovinces and bioprovinces—large and effectively isolated spatiotemporal structures of biota integrated internally by coevolution and individuated externally by a hierarchy of barriers. Gaia is here understood as the largest eco-genealogical individual compartmentalized by the outer space of the Earth and integrated at long time scales by biotic interactions and plate tectonic mixing of biota. The existence of a hierarchy of barriers and multilevel allopatry suggests that geographic isolation takes part not only in individuating species lineages, but also in producing coherent complexes of separate lineages forming bioprovinces at multiple space and time scales. The sizes, configurations, and durations of Bretskyan units are directly tied to geodynamics, demonstrating the central role of the physical planet in the processes of individuation and merging of geobiomes and the control of coevolution, and all its ramifications, at multiple space and time scales. The Bretskyan hierarchy also allows the integration of previously unconnected themes—“egalitarian” major transitions in individuality (e.g., eukaryogenesis) and some of the megatrajectories in the history of life—into a single theoretical framework of spatial and temporal scaling of eco-genealogy. The pervasive scaling of geodynamical processes and the direct connection of geodynamics to the dynamics of Bretskyan units allows us to formulate conjectures on the scales and limits of spatial and temporal contingency and competitiveness of biotas in evolution.
{"title":"The Bretskyan hierarchy, multiscale allopatry, and geobiomes—on the nature of evolutionary things","authors":"Andrej Spiridonov, Niles Eldredge","doi":"10.1017/pab.2023.37","DOIUrl":"https://doi.org/10.1017/pab.2023.37","url":null,"abstract":"<p>The process of evolution and the structures it produces are best understood in the light of hierarchy theory. The biota traditionally is described by either the genealogical Linnaean hierarchy or economic hierarchies of communities or ecosystems. Here we describe the Bretskyan hierarchy—a hybrid eco-genealogical hierarchy that consists of nested sets of different-sized, usually polyphyletic communities of interacting individuals separated from other such communities in space and time at multiple scales. The Bretskyan hierarchy consists of elements that have both genealogical and economic properties and functions—situated between, and connecting the elements of, the economic hierarchies (Vernadskyan) and the genealogical (Linnaean) hierarchy. The described hierarchy at lower tiers is populated by holobionts, individuals composed of multiple polyphyletic lineages integrated by functional interactions or biotically fabricated structures, such as membranes. At larger spatial tiers and longer time scales, the members of the Bretskyan hierarchy are of a more diffuse nature, partially due to the small size and relatively short duration of us as observers of larger and longer-lasting structures, here described as geobiomes. Their individuality is externally forced and directly tied to the spatial and temporal physical structures of our planet. These are sub-bioprovinces and bioprovinces—large and effectively isolated spatiotemporal structures of biota integrated internally by coevolution and individuated externally by a hierarchy of barriers. Gaia is here understood as the largest eco-genealogical individual compartmentalized by the outer space of the Earth and integrated at long time scales by biotic interactions and plate tectonic mixing of biota. The existence of a hierarchy of barriers and multilevel allopatry suggests that geographic isolation takes part not only in individuating species lineages, but also in producing coherent complexes of separate lineages forming bioprovinces at multiple space and time scales. The sizes, configurations, and durations of Bretskyan units are directly tied to geodynamics, demonstrating the central role of the physical planet in the processes of individuation and merging of geobiomes and the control of coevolution, and all its ramifications, at multiple space and time scales. The Bretskyan hierarchy also allows the integration of previously unconnected themes—“egalitarian” major transitions in individuality (e.g., eukaryogenesis) and some of the megatrajectories in the history of life—into a single theoretical framework of spatial and temporal scaling of eco-genealogy. The pervasive scaling of geodynamical processes and the direct connection of geodynamics to the dynamics of Bretskyan units allows us to formulate conjectures on the scales and limits of spatial and temporal contingency and competitiveness of biotas in evolution.</p>","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"16 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139657545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Isaac W. Krone, Katherine M. Magoulick, Ryan M. Yohler
We know the fossil record is incomplete, but just how much biodiversity does it miss? We produce the first geographically controlled estimate by comparing the geographic ranges of 34,266 modern tetrapods with a map of the world's sedimentary basins. By modeling which tetrapods live within sedimentary basins, we produce a first-order estimate of what might be found in the fossil record of the future. In this record, nearly 30% of tetrapod species have almost no chance of fossilizing, and more stringent criteria for fossilization exclude far more diversity. This geographically structured fossil record preserves disparate patterns of taxonomic and phylogenetic diversity in different tetrapod groups and underpreserves projected extinctions. For the globally threatened amphibians, the magnitude of the extinction of all endangered species would be underestimated by 66–98% in our future record. These results raise profound questions about the structure of the fossil record. Is it capable of recording major origination and extinction events on land? Have swaths of terrestrial diversity gone unrecorded based on geography alone? There are chapters of Earth history that paleontologists can never hope to know, but what is missing, and why?
{"title":"All the Earth will not remember: how geographic gaps structure the record of diversity and extinction","authors":"Isaac W. Krone, Katherine M. Magoulick, Ryan M. Yohler","doi":"10.1017/pab.2023.34","DOIUrl":"https://doi.org/10.1017/pab.2023.34","url":null,"abstract":"We know the fossil record is incomplete, but just how much biodiversity does it miss? We produce the first geographically controlled estimate by comparing the geographic ranges of 34,266 modern tetrapods with a map of the world's sedimentary basins. By modeling which tetrapods live within sedimentary basins, we produce a first-order estimate of what might be found in the fossil record of the future. In this record, nearly 30% of tetrapod species have almost no chance of fossilizing, and more stringent criteria for fossilization exclude far more diversity. This geographically structured fossil record preserves disparate patterns of taxonomic and phylogenetic diversity in different tetrapod groups and underpreserves projected extinctions. For the globally threatened amphibians, the magnitude of the extinction of all endangered species would be underestimated by 66–98% in our future record. These results raise profound questions about the structure of the fossil record. Is it capable of recording major origination and extinction events on land? Have swaths of terrestrial diversity gone unrecorded based on geography alone? There are chapters of Earth history that paleontologists can never hope to know, but what is missing, and why?","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"130 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139560302","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
During the late Miocene and early Pliocene (latest Hemphillian, Hh4 interval, 5.7 to 4.75 Ma) a distinctive suite of four species of extinct horses (Family Equidae) were widespread in North America. This includes Nannippus aztecus, Neohipparion eurystyle, Astrohippus stocki, and Dinohippus mexicanus. In Florida, two additional equid species, Pseudhipparion simpsoni and Cormohipparion emsliei, are also typically found at Hh4 localities. Here we compare horses from four Hh4 Florida fossil sites, including three from the Bone Valley mines and a fourth from the recently discovered Montbrook site. Two of these sites have all six expected species, one has five species, and one has only four species present. To explain these differences, we used species counts from research databases and rarefaction simulation to clarify the relative abundances, species richness, and occurrences of these horses from these four sites. The Palmetto Mine (Agrico) site, with five equid species, appears to lack the sixth species owing to ecological reasons. This is different from Montbrook, the site with only four of the six species. Results indicate that Montbrook is likely lacking two missing equid species for a couple of reasons: sampling bias and biological/ecological causes. Our results demonstrate that sampling biases can account for observed equid species richness when the overall abundance of certain equid species is low. Nevertheless, other factors, including ecology and with sufficient resolution, perhaps also time, may also explain the distribution and occurrences of individual species at these and other fossil sites. In a broader perspective, analyses such as this example provide an opportunity to address a persistent challenge in paleontology, that is, how do we explain absences of extinct taxa from the fossil record?
{"title":"Species occurrences of Mio-Pliocene horses (Equidae) from Florida: sampling, ecology, or both?","authors":"Stephanie R. Killingsworth, Bruce J. MacFadden","doi":"10.1017/pab.2023.35","DOIUrl":"https://doi.org/10.1017/pab.2023.35","url":null,"abstract":"During the late Miocene and early Pliocene (latest Hemphillian, Hh4 interval, 5.7 to 4.75 Ma) a distinctive suite of four species of extinct horses (Family Equidae) were widespread in North America. This includes <jats:italic>Nannippus aztecus</jats:italic>, <jats:italic>Neohipparion eurystyle</jats:italic>, <jats:italic>Astrohippus stocki</jats:italic>, and <jats:italic>Dinohippus mexicanus</jats:italic>. In Florida, two additional equid species, <jats:italic>Pseudhipparion simpsoni</jats:italic> and <jats:italic>Cormohipparion emsliei</jats:italic>, are also typically found at Hh4 localities. Here we compare horses from four Hh4 Florida fossil sites, including three from the Bone Valley mines and a fourth from the recently discovered Montbrook site. Two of these sites have all six expected species, one has five species, and one has only four species present. To explain these differences, we used species counts from research databases and rarefaction simulation to clarify the relative abundances, species richness, and occurrences of these horses from these four sites. The Palmetto Mine (Agrico) site, with five equid species, appears to lack the sixth species owing to ecological reasons. This is different from Montbrook, the site with only four of the six species. Results indicate that Montbrook is likely lacking two missing equid species for a couple of reasons: sampling bias and biological/ecological causes. Our results demonstrate that sampling biases can account for observed equid species richness when the overall abundance of certain equid species is low. Nevertheless, other factors, including ecology and with sufficient resolution, perhaps also time, may also explain the distribution and occurrences of individual species at these and other fossil sites. In a broader perspective, analyses such as this example provide an opportunity to address a persistent challenge in paleontology, that is, how do we explain absences of extinct taxa from the fossil record?","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"10 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139560237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jansen A. Smith, Nussaïbah B. Raja, Thomas Clements, Danijela Dimitrijević, Elizabeth M. Dowding, Emma M. Dunne, Bryan M. Gee, Pedro L. Godoy, Elizabeth M. Lombardi, Laura P. A. Mulvey, Paulina S. Nätscher, Carl J. Reddin, Bryan Shirley, Rachel C. M. Warnock, Ádám T. Kocsis
Data compilations expand the scope of research; however, data citation practice lags behind advances in data use. It remains uncommon for data users to credit data producers in professionally meaningful ways. In paleontology, databases like the Paleobiology Database (PBDB) enable assessment of patterns and processes spanning millions of years, up to global scale. The status quo for data citation creates an imbalance wherein publications drawing data from the PBDB receive significantly more citations (median: 4.3 ± 3.5 citations/year) than the publications producing the data (1.4 ± 1.3 citations/year). By accounting for data reuse where citations were neglected, the projected citation rate for data-provisioning publications approached parity (4.2 ± 2.2 citations/year) and the impact factor of paleontological journals (n = 55) increased by an average of 13.4% (maximum increase = 57.8%) in 2019. Without rebalancing the distribution of scientific credit, emerging “big data” research in paleontology—and science in general—is at risk of undercutting itself through a systematic devaluation of the work that is foundational to the discipline.
{"title":"Increasing the equitability of data citation in paleontology: capacity building for the big data future","authors":"Jansen A. Smith, Nussaïbah B. Raja, Thomas Clements, Danijela Dimitrijević, Elizabeth M. Dowding, Emma M. Dunne, Bryan M. Gee, Pedro L. Godoy, Elizabeth M. Lombardi, Laura P. A. Mulvey, Paulina S. Nätscher, Carl J. Reddin, Bryan Shirley, Rachel C. M. Warnock, Ádám T. Kocsis","doi":"10.1017/pab.2023.33","DOIUrl":"https://doi.org/10.1017/pab.2023.33","url":null,"abstract":"<p>Data compilations expand the scope of research; however, data citation practice lags behind advances in data use. It remains uncommon for data users to credit data producers in professionally meaningful ways. In paleontology, databases like the Paleobiology Database (PBDB) enable assessment of patterns and processes spanning millions of years, up to global scale. The status quo for data citation creates an imbalance wherein publications drawing data from the PBDB receive significantly more citations (median: 4.3 ± 3.5 citations/year) than the publications producing the data (1.4 ± 1.3 citations/year). By accounting for data reuse where citations were neglected, the projected citation rate for data-provisioning publications approached parity (4.2 ± 2.2 citations/year) and the impact factor of paleontological journals (<span>n</span> = 55) increased by an average of 13.4% (maximum increase = 57.8%) in 2019. Without rebalancing the distribution of scientific credit, emerging “big data” research in paleontology—and science in general—is at risk of undercutting itself through a systematic devaluation of the work that is foundational to the discipline.</p>","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"125 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139052913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Women are underrepresented in paleontology. Despite more women students, representation at senior levels remains low. To advance professionally, scientists must disseminate their research through peer-reviewed publications. We examine gendered authorship patterns in Paleobiology to ask whether the publishing infrastructure supports the Paleontological Society's gender-equity goals. We reviewed all papers published in Paleobiology from its inception in 1975 through 2021. For each paper, we recorded each author, the author's position in the author list, and the total number of authors on each paper. We coded gender based on a combination of personal communication and pronouns used in publicly available information. We compared author demographics with anonymized membership data from the Paleontological Society. Over the journal's run, the number of authors per paper increased due to cultural shifts toward collaborative work and acknowledging student contributions with coauthorship. These trends contribute to proportionally more women authors, beginning in the early 2000s. Despite these increases, women remain chronically underrepresented. In 2018, 2019, and 2021, the proportion of women authors in Paleobiology paralleled membership in the Paleontological Society. However, in 2020, Paleobiology published fewer women authors than expected based on society membership. This echoes declines in women's scholarly productivity in the first year of the COVID-19 pandemic observed across many disciplines. We offer four recommendations: (1) practice double-anonymous peer review; (2) recruit editors from diverse backgrounds who invite reviewers with diverse backgrounds; (3) democratize manuscript review by selecting reviewers from a disaggregated reviewer database; and (4) gather and analyze demographic data for both submissions and publications.
{"title":"Repairing the scaffolding: women authors in Paleobiology","authors":"Nan Crystal Arens, Levi Holguin, Natalie Sandoval","doi":"10.1017/pab.2023.32","DOIUrl":"https://doi.org/10.1017/pab.2023.32","url":null,"abstract":"<p>Women are underrepresented in paleontology. Despite more women students, representation at senior levels remains low. To advance professionally, scientists must disseminate their research through peer-reviewed publications. We examine gendered authorship patterns in <span>Paleobiology</span> to ask whether the publishing infrastructure supports the Paleontological Society's gender-equity goals. We reviewed all papers published in <span>Paleobiology</span> from its inception in 1975 through 2021. For each paper, we recorded each author, the author's position in the author list, and the total number of authors on each paper. We coded gender based on a combination of personal communication and pronouns used in publicly available information. We compared author demographics with anonymized membership data from the Paleontological Society. Over the journal's run, the number of authors per paper increased due to cultural shifts toward collaborative work and acknowledging student contributions with coauthorship. These trends contribute to proportionally more women authors, beginning in the early 2000s. Despite these increases, women remain chronically underrepresented. In 2018, 2019, and 2021, the proportion of women authors in <span>Paleobiology</span> paralleled membership in the Paleontological Society. However, in 2020, <span>Paleobiology</span> published fewer women authors than expected based on society membership. This echoes declines in women's scholarly productivity in the first year of the COVID-19 pandemic observed across many disciplines. We offer four recommendations: (1) practice double-anonymous peer review; (2) recruit editors from diverse backgrounds who invite reviewers with diverse backgrounds; (3) democratize manuscript review by selecting reviewers from a disaggregated reviewer database; and (4) gather and analyze demographic data for both submissions and publications.</p>","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"33 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138548309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Strata of the Ediacaran Period (635–538.8 Ma) yield the oldest known fossils of complex, macroscopic organisms in the geologic record. These “Ediacaran-type” macrofossils (known as the Ediacaran biota) first appear in mid-Ediacaran strata, experience an apparent decline through the terminal Ediacaran, and directly precede the Cambrian (538.8–485.4 Ma) radiation of animals. Existing hypotheses for the origin and demise of the Ediacaran biota include: changing oceanic redox states, biotic replacement by succeeding Cambrian-type fauna, and mass extinction driven by environmental change. Few studies frame trends in Ediacaran and Cambrian macroevolution from the perspective of the sedimentary rock record, despite well-documented Phanerozoic covariation of macroevolutionary patterns and sedimentary rock quantity. Here we present a quantitative analysis of North American Ediacaran–Cambrian rock and fossil records from Macrostrat and the Paleobiology Database. Marine sedimentary rock quantity increases nearly monotonically and by more than a factor of five from the latest Ediacaran to the late Cambrian. Ediacaran–Cambrian fossil quantities exhibit a comparable trajectory and have strong (rs > 0.8) positive correlations with marine sedimentary area and volume flux at multiple temporal resolutions. Even so, Ediacaran fossil quantities are dramatically reduced in comparison to the Cambrian when normalized by the quantity of preserved marine rock. Although aspects of these results are consistent with the expectations of a simple fossil preservation–induced sampling bias, together they suggest that transgression–regression and a large expansion of marine shelf environments coincided with the diversification of animals during a dramatic transition that is starkly evident in both the sedimentary rock and fossil records.
{"title":"Transgression–regression cycles drive correlations in Ediacaran–Cambrian rock and fossil records","authors":"Daniel C. Segessenman, Shanan E. Peters","doi":"10.1017/pab.2023.31","DOIUrl":"https://doi.org/10.1017/pab.2023.31","url":null,"abstract":"Strata of the Ediacaran Period (635–538.8 Ma) yield the oldest known fossils of complex, macroscopic organisms in the geologic record. These “Ediacaran-type” macrofossils (known as the Ediacaran biota) first appear in mid-Ediacaran strata, experience an apparent decline through the terminal Ediacaran, and directly precede the Cambrian (538.8–485.4 Ma) radiation of animals. Existing hypotheses for the origin and demise of the Ediacaran biota include: changing oceanic redox states, biotic replacement by succeeding Cambrian-type fauna, and mass extinction driven by environmental change. Few studies frame trends in Ediacaran and Cambrian macroevolution from the perspective of the sedimentary rock record, despite well-documented Phanerozoic covariation of macroevolutionary patterns and sedimentary rock quantity. Here we present a quantitative analysis of North American Ediacaran–Cambrian rock and fossil records from Macrostrat and the Paleobiology Database. Marine sedimentary rock quantity increases nearly monotonically and by more than a factor of five from the latest Ediacaran to the late Cambrian. Ediacaran–Cambrian fossil quantities exhibit a comparable trajectory and have strong (<jats:italic>r</jats:italic><jats:sub>s</jats:sub> > 0.8) positive correlations with marine sedimentary area and volume flux at multiple temporal resolutions. Even so, Ediacaran fossil quantities are dramatically reduced in comparison to the Cambrian when normalized by the quantity of preserved marine rock. Although aspects of these results are consistent with the expectations of a simple fossil preservation–induced sampling bias, together they suggest that transgression–regression and a large expansion of marine shelf environments coincided with the diversification of animals during a dramatic transition that is starkly evident in both the sedimentary rock and fossil records.","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"181 ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138505205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Caroline P. Abbott, Mark Webster, Kenneth D. Angielczyk
Body size has a long history of study in paleobiology and underlies many important phenomena in macroevolution. Body-size patterns in the fossil record are often examined by utilizing size data alone, which hinders our ability to describe the biological meaning behind size change on macroevolutionary timescales. Without data reflecting the biological and geologic factors that drive size change, we cannot assess its mechanistic underpinnings. Existing frameworks for studying ontogeny and phylogeny can remedy this problem, particularly the classic age–size–“shape” space originally developed for studies of heterochrony. When evaluated based on metrics for age, size, and phenotype in populations, proposed mechanisms for size change can be outlined theoretically and tested empirically in the record. Using this framework, we can compare ontogenetic trajectories within and between species and determine how changes in size emerge. Here, we outline ontogenetic mechanisms for evolutionary size change, such as heterochrony, as well as how geologic factors can drive apparent, non-biological size change (e.g., taphonomic size sorting). To demonstrate the utility of this framework in actual paleobiological problems, we apply it to the Lilliput effect, a compelling and widely documented pattern of size decrease during extinction events. However, little is known about the mechanisms underlying this pattern. We provide a brief history of the Lilliput effect and refine its definition in a framework that can be mechanistically tested. Processes that likely produce Lilliput effects include allometric and sequence repatterning (including heterochrony) and evolutionary size-selective sorting. We describe these mechanisms and highlight relevant examples of the Lilliput effect for which feasible empirical tests are possible.
{"title":"Ontogenetic mechanisms of size change: implications for the Lilliput effect and beyond","authors":"Caroline P. Abbott, Mark Webster, Kenneth D. Angielczyk","doi":"10.1017/pab.2023.26","DOIUrl":"https://doi.org/10.1017/pab.2023.26","url":null,"abstract":"Body size has a long history of study in paleobiology and underlies many important phenomena in macroevolution. Body-size patterns in the fossil record are often examined by utilizing size data alone, which hinders our ability to describe the biological meaning behind size change on macroevolutionary timescales. Without data reflecting the biological and geologic factors that drive size change, we cannot assess its mechanistic underpinnings. Existing frameworks for studying ontogeny and phylogeny can remedy this problem, particularly the classic age–size–“shape” space originally developed for studies of heterochrony. When evaluated based on metrics for age, size, and phenotype in populations, proposed mechanisms for size change can be outlined theoretically and tested empirically in the record. Using this framework, we can compare ontogenetic trajectories within and between species and determine how changes in size emerge. Here, we outline ontogenetic mechanisms for evolutionary size change, such as heterochrony, as well as how geologic factors can drive apparent, non-biological size change (e.g., taphonomic size sorting). To demonstrate the utility of this framework in actual paleobiological problems, we apply it to the Lilliput effect, a compelling and widely documented pattern of size decrease during extinction events. However, little is known about the mechanisms underlying this pattern. We provide a brief history of the Lilliput effect and refine its definition in a framework that can be mechanistically tested. Processes that likely produce Lilliput effects include allometric and sequence repatterning (including heterochrony) and evolutionary size-selective sorting. We describe these mechanisms and highlight relevant examples of the Lilliput effect for which feasible empirical tests are possible.","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"185 ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138505203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Late Triassic conodont species Mockina ex gr. carinata and Mockina ex gr. englandi were exceptionally prevalent among the marine fauna of the Panthalassan realm from the middle Norian through to the Rhaetian. Leading into the complete extinction of conodonts near the Triassic/Jurassic boundary, a significant turnover event occurred in conodont fauna across the Norian/Rhaetian boundary (NRB), with the pectiniform elements of common Rhaetian genera from Tethys exhibiting minimal or absent platforms. This intergeneric trend of platform reduction is not as evident in Panthalassa, where these genera are very rare, but morphometric analyses of M. ex gr. carinata and M. ex gr. englandi specimens from across the Canadian Cordillera demonstrate that comparable shifts in morphology occurred intraspecifically in Panthalassa across the NRB, confirming the global extent of these trends. Pectiniform elements of M. ex gr. carinata display a sequential reduction of platform width from the middle Norian to late Norian to Rhaetian, whereas pectiniform elements of M. ex gr. englandi display a reduction of platform width only from the late Norian to Rhaetian. Specimens of both species that have a mid-platform length to breadth ratio greater than 3:1 are restricted to the Rhaetian. Specimens from the Kennecott Point section on Haida Gwaii, British Columbia, demonstrate that this morphological shift occurred somewhat later than other biostratigraphic proxies for the NRB. The global trend of platform width reduction in many conodont pectiniform elements may reflect a change in primary diet away from hard food sources, perhaps suggesting some degree of carbonate biomineralization suppression beginning around the NRB. This interpretation would support CO2 outgassing as the causal mechanism of the environmental disturbance at the NRB and identify the NRB as a significant turning point for Late Triassic ecosystems, marking the beginning of a protracted, multiphase end-Triassic mass extinction.
晚三叠世牙形刺物种Mockina ex gr. carinata和Mockina ex gr. englandi在中诺里亚到雷提亚的泛地中海王国的海洋动物群中特别普遍。在三叠纪/侏罗纪边界附近的牙形刺完全灭绝之前,在Norian/Rhaetian边界(NRB)的牙形刺动物群中发生了一次重大的更替事件,来自Tethys的常见Rhaetian属的pectinform元素显示出很少或没有平台。这种台地减少的属间趋势在Panthalassa中并不明显,因为这些属在那里非常罕见,但对加拿大科迪勒拉地区的M. ex gr. carinata和M. ex gr. englandi标本的形态测量学分析表明,在整个NRB的Panthalassa中,形态上的类似变化发生在种内,证实了这些趋势的全球范围。m.ex gr. carinata的pectinform元素表现出中诺里亚-晚诺里亚-雷蒂亚的台地宽度递减,而m.ex gr. englandi的pectinform元素只表现出晚诺里亚-雷蒂亚台地宽度递减。这两个物种的标本中平台的长度与宽度比大于3:1仅限于雷蒂亚。来自不列颠哥伦比亚省海达瓜伊的Kennecott Point剖面的标本表明,这种形态转变发生的时间比其他生物地层代用物要晚。许多牙形石果胶状元素的平台宽度减少的全球趋势可能反映了原始饮食从硬食物来源的变化,可能表明在NRB周围开始某种程度的碳酸盐生物矿化抑制。这一解释将支持二氧化碳脱气作为北海带环境扰动的因果机制,并将北海带确定为晚三叠纪生态系统的一个重要转折点,标志着一场旷日持久的、多阶段的三叠纪末期大灭绝的开始。
{"title":"Morphological trends across the Norian/Rhaetian boundary within Late Triassic conodonts in western Canada: implications for protracted paleoenvironmental disturbance preceding the end-Triassic mass extinction","authors":"Jerry Z. X. Lei, Martyn L. Golding, Jon M. Husson","doi":"10.1017/pab.2023.30","DOIUrl":"https://doi.org/10.1017/pab.2023.30","url":null,"abstract":"The Late Triassic conodont species <jats:italic>Mockina</jats:italic> ex gr. <jats:italic>carinata</jats:italic> and <jats:italic>Mockina</jats:italic> ex gr. <jats:italic>englandi</jats:italic> were exceptionally prevalent among the marine fauna of the Panthalassan realm from the middle Norian through to the Rhaetian. Leading into the complete extinction of conodonts near the Triassic/Jurassic boundary, a significant turnover event occurred in conodont fauna across the Norian/Rhaetian boundary (NRB), with the pectiniform elements of common Rhaetian genera from Tethys exhibiting minimal or absent platforms. This intergeneric trend of platform reduction is not as evident in Panthalassa, where these genera are very rare, but morphometric analyses of <jats:italic>M.</jats:italic> ex gr. <jats:italic>carinata</jats:italic> and <jats:italic>M.</jats:italic> ex gr. <jats:italic>englandi</jats:italic> specimens from across the Canadian Cordillera demonstrate that comparable shifts in morphology occurred intraspecifically in Panthalassa across the NRB, confirming the global extent of these trends. Pectiniform elements of <jats:italic>M.</jats:italic> ex gr. <jats:italic>carinata</jats:italic> display a sequential reduction of platform width from the middle Norian to late Norian to Rhaetian, whereas pectiniform elements of <jats:italic>M.</jats:italic> ex gr. <jats:italic>englandi</jats:italic> display a reduction of platform width only from the late Norian to Rhaetian. Specimens of both species that have a mid-platform length to breadth ratio greater than 3:1 are restricted to the Rhaetian. Specimens from the Kennecott Point section on Haida Gwaii, British Columbia, demonstrate that this morphological shift occurred somewhat later than other biostratigraphic proxies for the NRB. The global trend of platform width reduction in many conodont pectiniform elements may reflect a change in primary diet away from hard food sources, perhaps suggesting some degree of carbonate biomineralization suppression beginning around the NRB. This interpretation would support CO<jats:sub>2</jats:sub> outgassing as the causal mechanism of the environmental disturbance at the NRB and identify the NRB as a significant turning point for Late Triassic ecosystems, marking the beginning of a protracted, multiphase end-Triassic mass extinction.","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"182 ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138505204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01Epub Date: 2023-04-17DOI: 10.1017/pab.2023.10
Kjetil Lysne Voje
The nature of phenotypic evolution within lineages is central to many unresolved questions in paleontology and evolutionary biology. Analyses of evolutionary time-series of ancestor-descendant populations in the fossil record are likely to make important contributions to many of these debates. However, the limited number of models that have been applied to these types of data may restrict our ability to interpret phenotypic evolution in the fossil record. Using uni- and multivariate models of trait evolution that make different assumptions regarding the dynamics of the adaptive landscape, I evaluate contrasting hypotheses to explain evolution of size in the radiolarian Eucyrtidium calvertense and armor in the stickleback Gaserosteus doryssus. Body size evolution in E. calvertense is best explained by a model where the lineage evolves as a consequence of a shift in the adaptive landscape that coincides with the initiation of neosympatry with its sister lineage. Multivariate evolution of armor traits in a stickleback lineage (Gasterosteus doryssus) show evidence of adaptation towards independent optima on the adaptive landscape at the same time as traits change in a correlated fashion. The fitted models are available in a the R package evoTS, which builds on the commonly used paleoTS framework.
{"title":"Fitting and evaluating univariate and multivariate models of within-lineage evolution.","authors":"Kjetil Lysne Voje","doi":"10.1017/pab.2023.10","DOIUrl":"10.1017/pab.2023.10","url":null,"abstract":"<p><p>The nature of phenotypic evolution within lineages is central to many unresolved questions in paleontology and evolutionary biology. Analyses of evolutionary time-series of ancestor-descendant populations in the fossil record are likely to make important contributions to many of these debates. However, the limited number of models that have been applied to these types of data may restrict our ability to interpret phenotypic evolution in the fossil record. Using uni- and multivariate models of trait evolution that make different assumptions regarding the dynamics of the adaptive landscape, I evaluate contrasting hypotheses to explain evolution of size in the radiolarian <i>Eucyrtidium calvertense</i> and armor in the stickleback <i>Gaserosteus doryssus</i>. Body size evolution in <i>E. calvertense</i> is best explained by a model where the lineage evolves as a consequence of a shift in the adaptive landscape that coincides with the initiation of neosympatry with its sister lineage. Multivariate evolution of armor traits in a stickleback lineage (<i>Gasterosteus doryssus</i>) show evidence of adaptation towards independent optima on the adaptive landscape at the same time as traits change in a correlated fashion. The fitted models are available in a the R package evoTS, which builds on the commonly used paleoTS framework.</p>","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"49 1","pages":"747-764"},"PeriodicalIF":2.7,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7615219/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46998732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}