Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents
Why some clades are more species-rich than others is a central question in macroevolution. Most hypotheses explaining exceptionally diverse clades involve the emergence of an ecological opportunity caused by a major biogeographic transition or evolution of a key innovation. The radiation of muroid r...
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ftdryad:oai:v1.datadryad.org:10255/dryad.47245 2023-05-15T13:38:10+02:00 Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents Schenk, John J. Rowe, Kevin C. Steppan, Scott J. South America Sahul 2013-08-05T15:52:09Z http://hdl.handle.net/10255/dryad.47245 https://doi.org/10.5061/dryad.dc34q unknown doi:10.5061/dryad.dc34q/1 doi:10.5061/dryad.dc34q/2 doi:10.5061/dryad.dc34q/3 doi:10.5061/dryad.dc34q/4 doi:10.5061/dryad.dc34q/5 doi:10.1093/sysbio/syt050 PMID:23925508 doi:10.5061/dryad.dc34q Schenk JJ, Rowe KC, Steppan SJ (2013) Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents. Systematic Biology 62(6): 837-864. http://hdl.handle.net/10255/dryad.47245 adaptive radiation diversification historical biogeography mammals phylogenetics Article 2013 ftdryad https://doi.org/10.5061/dryad.dc34q https://doi.org/10.5061/dryad.dc34q/1 https://doi.org/10.5061/dryad.dc34q/2 https://doi.org/10.5061/dryad.dc34q/3 https://doi.org/10.5061/dryad.dc34q/4 https://doi.org/10.5061/dryad.dc34q/5 https://doi.org/1 2020-01-01T15:00:19Z Why some clades are more species-rich than others is a central question in macroevolution. Most hypotheses explaining exceptionally diverse clades involve the emergence of an ecological opportunity caused by a major biogeographic transition or evolution of a key innovation. The radiation of muroid rodents is an ideal model for testing theories of diversification rates in relation to biogeography and ecological opportunity because the group is exceptionally species-rich (comprising nearly one-third of all mammal species), it is ecologically diverse, and it has colonized every major landmass except New Zealand and Antarctica, thus providing multiple replicate radiations. We present an extension of the conventional ecological opportunity model to include a geographic incumbency effect, develop the largest muroid phylogeny to date, and use this phylogeny to test the new model. The nearly 300-species phylogeny based on four nuclear genes is robustly resolved throughout. Consistent with the fossil record, we identified Eurasia as the most likely origin of the group and reconstructed five to seven colonizations of Africa, five of North America, four of Southeast Asia, two of South America, two of Sahul, one of Madagascar, and eight to ten recolonizations of Eurasia. We accounted for incomplete taxon sampling by using multiple statistical methods and identified three corroborated regions of the tree with significant shifts in diversification rates. In several cases, higher rates were associated with the first colonization of a continental area, but most colonizations were not followed by bursts of speciation. We found strong evidence for diversification consistent with the ecological opportunity model (initial burst followed by density-dependent slowdown) in the first colonization of South America and partial support for this model in the first colonization of Sahul. Primary colonizers appear to inhibit the ultimate diversity of secondary colonizers, a pattern of incumbency that is consistent with ecological opportunity, but they did not inhibit initial diversification rates of secondary colonizers. These results indicate that ecological opportunity may be a general but weak process in muroids and one that requires specific circumstances to lead to an adaptive radiation. The total land area, length of time between colonizations, and rank of colonizations did not influence the diversification rates of primary colonizers. Models currently employed to test ecological opportunity do a poor job of explaining muroid diversity. In addition, the various rate-shift metrics identified different clades, suggesting that caution should be used when only one is applied, and we discuss which methods are most appropriate to address different questions of diversification. Article in Journal/Newspaper Antarc* Antarctica Dryad Digital Repository (Duke University) New Zealand |
institution |
Open Polar |
collection |
Dryad Digital Repository (Duke University) |
op_collection_id |
ftdryad |
language |
unknown |
topic |
adaptive radiation diversification historical biogeography mammals phylogenetics |
spellingShingle |
adaptive radiation diversification historical biogeography mammals phylogenetics Schenk, John J. Rowe, Kevin C. Steppan, Scott J. Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
topic_facet |
adaptive radiation diversification historical biogeography mammals phylogenetics |
description |
Why some clades are more species-rich than others is a central question in macroevolution. Most hypotheses explaining exceptionally diverse clades involve the emergence of an ecological opportunity caused by a major biogeographic transition or evolution of a key innovation. The radiation of muroid rodents is an ideal model for testing theories of diversification rates in relation to biogeography and ecological opportunity because the group is exceptionally species-rich (comprising nearly one-third of all mammal species), it is ecologically diverse, and it has colonized every major landmass except New Zealand and Antarctica, thus providing multiple replicate radiations. We present an extension of the conventional ecological opportunity model to include a geographic incumbency effect, develop the largest muroid phylogeny to date, and use this phylogeny to test the new model. The nearly 300-species phylogeny based on four nuclear genes is robustly resolved throughout. Consistent with the fossil record, we identified Eurasia as the most likely origin of the group and reconstructed five to seven colonizations of Africa, five of North America, four of Southeast Asia, two of South America, two of Sahul, one of Madagascar, and eight to ten recolonizations of Eurasia. We accounted for incomplete taxon sampling by using multiple statistical methods and identified three corroborated regions of the tree with significant shifts in diversification rates. In several cases, higher rates were associated with the first colonization of a continental area, but most colonizations were not followed by bursts of speciation. We found strong evidence for diversification consistent with the ecological opportunity model (initial burst followed by density-dependent slowdown) in the first colonization of South America and partial support for this model in the first colonization of Sahul. Primary colonizers appear to inhibit the ultimate diversity of secondary colonizers, a pattern of incumbency that is consistent with ecological opportunity, but they did not inhibit initial diversification rates of secondary colonizers. These results indicate that ecological opportunity may be a general but weak process in muroids and one that requires specific circumstances to lead to an adaptive radiation. The total land area, length of time between colonizations, and rank of colonizations did not influence the diversification rates of primary colonizers. Models currently employed to test ecological opportunity do a poor job of explaining muroid diversity. In addition, the various rate-shift metrics identified different clades, suggesting that caution should be used when only one is applied, and we discuss which methods are most appropriate to address different questions of diversification. |
format |
Article in Journal/Newspaper |
author |
Schenk, John J. Rowe, Kevin C. Steppan, Scott J. |
author_facet |
Schenk, John J. Rowe, Kevin C. Steppan, Scott J. |
author_sort |
Schenk, John J. |
title |
Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
title_short |
Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
title_full |
Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
title_fullStr |
Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
title_full_unstemmed |
Data from: Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
title_sort |
data from: ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents |
publishDate |
2013 |
url |
http://hdl.handle.net/10255/dryad.47245 https://doi.org/10.5061/dryad.dc34q |
op_coverage |
South America Sahul |
geographic |
New Zealand |
geographic_facet |
New Zealand |
genre |
Antarc* Antarctica |
genre_facet |
Antarc* Antarctica |
op_relation |
doi:10.5061/dryad.dc34q/1 doi:10.5061/dryad.dc34q/2 doi:10.5061/dryad.dc34q/3 doi:10.5061/dryad.dc34q/4 doi:10.5061/dryad.dc34q/5 doi:10.1093/sysbio/syt050 PMID:23925508 doi:10.5061/dryad.dc34q Schenk JJ, Rowe KC, Steppan SJ (2013) Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents. Systematic Biology 62(6): 837-864. http://hdl.handle.net/10255/dryad.47245 |
op_doi |
https://doi.org/10.5061/dryad.dc34q https://doi.org/10.5061/dryad.dc34q/1 https://doi.org/10.5061/dryad.dc34q/2 https://doi.org/10.5061/dryad.dc34q/3 https://doi.org/10.5061/dryad.dc34q/4 https://doi.org/10.5061/dryad.dc34q/5 https://doi.org/1 |
_version_ |
1766102169873809408 |