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Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus

The evolution of sustained plant–animal interactions depends critically upon genetic variation in the fitness benefits from the interaction. Genetic analyses of such interactions are limited to a few model systems, in part because genetic variation may be absent or the interacting species may be exp...

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Autores principales: Shortlidge, Erin E., Carey, Sarah B., Payton, Adam C., McDaniel, Stuart F., Rosenstiel, Todd N., Eppley, Sarah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059975/
https://www.ncbi.nlm.nih.gov/pubmed/33784868
http://dx.doi.org/10.1098/rspb.2021.0119
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author Shortlidge, Erin E.
Carey, Sarah B.
Payton, Adam C.
McDaniel, Stuart F.
Rosenstiel, Todd N.
Eppley, Sarah M.
author_facet Shortlidge, Erin E.
Carey, Sarah B.
Payton, Adam C.
McDaniel, Stuart F.
Rosenstiel, Todd N.
Eppley, Sarah M.
author_sort Shortlidge, Erin E.
collection PubMed
description The evolution of sustained plant–animal interactions depends critically upon genetic variation in the fitness benefits from the interaction. Genetic analyses of such interactions are limited to a few model systems, in part because genetic variation may be absent or the interacting species may be experimentally intractable. Here, we examine the role of sperm-dispersing microarthropods in shaping reproduction and genetic variation in mosses. We established experimental mesocosms with known moss genotypes and inferred the parents of progeny from mesocosms with and without microarthropods, using a pooled sequencing approach. Moss reproductive rates increased fivefold in the presence of microarthropods, relative to control mesocosms. Furthermore, the presence of microarthropods increased the total number of reproducing moss genotypes, and changed the rank-order of fitness of male and female moss genotypes. Interestingly, the genotypes that reproduced most frequently did not produce sporophytes with the most spores, highlighting the challenge of defining fitness in mosses. These results demonstrate that microarthropods provide a fitness benefit for mosses, and highlight the potential for biotic dispersal agents to alter fitness among moss genotypes.
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spelling pubmed-80599752021-05-15 Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus Shortlidge, Erin E. Carey, Sarah B. Payton, Adam C. McDaniel, Stuart F. Rosenstiel, Todd N. Eppley, Sarah M. Proc Biol Sci Evolution The evolution of sustained plant–animal interactions depends critically upon genetic variation in the fitness benefits from the interaction. Genetic analyses of such interactions are limited to a few model systems, in part because genetic variation may be absent or the interacting species may be experimentally intractable. Here, we examine the role of sperm-dispersing microarthropods in shaping reproduction and genetic variation in mosses. We established experimental mesocosms with known moss genotypes and inferred the parents of progeny from mesocosms with and without microarthropods, using a pooled sequencing approach. Moss reproductive rates increased fivefold in the presence of microarthropods, relative to control mesocosms. Furthermore, the presence of microarthropods increased the total number of reproducing moss genotypes, and changed the rank-order of fitness of male and female moss genotypes. Interestingly, the genotypes that reproduced most frequently did not produce sporophytes with the most spores, highlighting the challenge of defining fitness in mosses. These results demonstrate that microarthropods provide a fitness benefit for mosses, and highlight the potential for biotic dispersal agents to alter fitness among moss genotypes. The Royal Society 2021-03-31 2021-03-31 /pmc/articles/PMC8059975/ /pubmed/33784868 http://dx.doi.org/10.1098/rspb.2021.0119 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Shortlidge, Erin E.
Carey, Sarah B.
Payton, Adam C.
McDaniel, Stuart F.
Rosenstiel, Todd N.
Eppley, Sarah M.
Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title_full Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title_fullStr Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title_full_unstemmed Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title_short Microarthropod contributions to fitness variation in the common moss Ceratodon purpureus
title_sort microarthropod contributions to fitness variation in the common moss ceratodon purpureus
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059975/
https://www.ncbi.nlm.nih.gov/pubmed/33784868
http://dx.doi.org/10.1098/rspb.2021.0119
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