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Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally

Biotic and abiotic factors interact with dominant plants—the locally most frequent or with the largest coverage—and nondominant plants differently, partially because dominant plants modify the environment where nondominant plants grow. For instance, if dominant plants compete strongly, they will dep...

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Autores principales: Arnillas, Carlos Alberto, Borer, Elizabeth T., Seabloom, Eric W., Alberti, Juan, Baez, Selene, Bakker, Jonathan D., Boughton, Elizabeth H., Buckley, Yvonne M., Bugalho, Miguel Nuno, Donohue, Ian, Dwyer, John, Firn, Jennifer, Gridzak, Riley, Hagenah, Nicole, Hautier, Yann, Helm, Aveliina, Jentsch, Anke, Knops, Johannes M. H., Komatsu, Kimberly J., Laanisto, Lauri, Laungani, Ramesh, McCulley, Rebecca, Moore, Joslin L., Morgan, John W., Peri, Pablo Luis, Power, Sally A., Price, Jodi, Sankaran, Mahesh, Schamp, Brandon, Speziale, Karina, Standish, Rachel, Virtanen, Risto, Cadotte, Marc W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717298/
https://www.ncbi.nlm.nih.gov/pubmed/35003636
http://dx.doi.org/10.1002/ece3.8266
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author Arnillas, Carlos Alberto
Borer, Elizabeth T.
Seabloom, Eric W.
Alberti, Juan
Baez, Selene
Bakker, Jonathan D.
Boughton, Elizabeth H.
Buckley, Yvonne M.
Bugalho, Miguel Nuno
Donohue, Ian
Dwyer, John
Firn, Jennifer
Gridzak, Riley
Hagenah, Nicole
Hautier, Yann
Helm, Aveliina
Jentsch, Anke
Knops, Johannes M. H.
Komatsu, Kimberly J.
Laanisto, Lauri
Laungani, Ramesh
McCulley, Rebecca
Moore, Joslin L.
Morgan, John W.
Peri, Pablo Luis
Power, Sally A.
Price, Jodi
Sankaran, Mahesh
Schamp, Brandon
Speziale, Karina
Standish, Rachel
Virtanen, Risto
Cadotte, Marc W.
author_facet Arnillas, Carlos Alberto
Borer, Elizabeth T.
Seabloom, Eric W.
Alberti, Juan
Baez, Selene
Bakker, Jonathan D.
Boughton, Elizabeth H.
Buckley, Yvonne M.
Bugalho, Miguel Nuno
Donohue, Ian
Dwyer, John
Firn, Jennifer
Gridzak, Riley
Hagenah, Nicole
Hautier, Yann
Helm, Aveliina
Jentsch, Anke
Knops, Johannes M. H.
Komatsu, Kimberly J.
Laanisto, Lauri
Laungani, Ramesh
McCulley, Rebecca
Moore, Joslin L.
Morgan, John W.
Peri, Pablo Luis
Power, Sally A.
Price, Jodi
Sankaran, Mahesh
Schamp, Brandon
Speziale, Karina
Standish, Rachel
Virtanen, Risto
Cadotte, Marc W.
author_sort Arnillas, Carlos Alberto
collection PubMed
description Biotic and abiotic factors interact with dominant plants—the locally most frequent or with the largest coverage—and nondominant plants differently, partially because dominant plants modify the environment where nondominant plants grow. For instance, if dominant plants compete strongly, they will deplete most resources, forcing nondominant plants into a narrower niche space. Conversely, if dominant plants are constrained by the environment, they might not exhaust available resources but instead may ameliorate environmental stressors that usually limit nondominants. Hence, the nature of interactions among nondominant species could be modified by dominant species. Furthermore, these differences could translate into a disparity in the phylogenetic relatedness among dominants compared to the relatedness among nondominants. By estimating phylogenetic dispersion in 78 grasslands across five continents, we found that dominant species were clustered (e.g., co‐dominant grasses), suggesting dominant species are likely organized by environmental filtering, and that nondominant species were either randomly assembled or overdispersed. Traits showed similar trends for those sites (<50%) with sufficient trait data. Furthermore, several lineages scattered in the phylogeny had more nondominant species than expected at random, suggesting that traits common in nondominants are phylogenetically conserved and have evolved multiple times. We also explored environmental drivers of the dominant/nondominant disparity. We found different assembly patterns for dominants and nondominants, consistent with asymmetries in assembly mechanisms. Among the different postulated mechanisms, our results suggest two complementary hypotheses seldom explored: (1) Nondominant species include lineages adapted to thrive in the environment generated by dominant species. (2) Even when dominant species reduce resources to nondominant ones, dominant species could have a stronger positive effect on some nondominants by ameliorating environmental stressors affecting them, than by depleting resources and increasing the environmental stress to those nondominants. These results show that the dominant/nondominant asymmetry has ecological and evolutionary consequences fundamental to understand plant communities.
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spelling pubmed-87172982022-01-06 Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally Arnillas, Carlos Alberto Borer, Elizabeth T. Seabloom, Eric W. Alberti, Juan Baez, Selene Bakker, Jonathan D. Boughton, Elizabeth H. Buckley, Yvonne M. Bugalho, Miguel Nuno Donohue, Ian Dwyer, John Firn, Jennifer Gridzak, Riley Hagenah, Nicole Hautier, Yann Helm, Aveliina Jentsch, Anke Knops, Johannes M. H. Komatsu, Kimberly J. Laanisto, Lauri Laungani, Ramesh McCulley, Rebecca Moore, Joslin L. Morgan, John W. Peri, Pablo Luis Power, Sally A. Price, Jodi Sankaran, Mahesh Schamp, Brandon Speziale, Karina Standish, Rachel Virtanen, Risto Cadotte, Marc W. Ecol Evol Research Articles Biotic and abiotic factors interact with dominant plants—the locally most frequent or with the largest coverage—and nondominant plants differently, partially because dominant plants modify the environment where nondominant plants grow. For instance, if dominant plants compete strongly, they will deplete most resources, forcing nondominant plants into a narrower niche space. Conversely, if dominant plants are constrained by the environment, they might not exhaust available resources but instead may ameliorate environmental stressors that usually limit nondominants. Hence, the nature of interactions among nondominant species could be modified by dominant species. Furthermore, these differences could translate into a disparity in the phylogenetic relatedness among dominants compared to the relatedness among nondominants. By estimating phylogenetic dispersion in 78 grasslands across five continents, we found that dominant species were clustered (e.g., co‐dominant grasses), suggesting dominant species are likely organized by environmental filtering, and that nondominant species were either randomly assembled or overdispersed. Traits showed similar trends for those sites (<50%) with sufficient trait data. Furthermore, several lineages scattered in the phylogeny had more nondominant species than expected at random, suggesting that traits common in nondominants are phylogenetically conserved and have evolved multiple times. We also explored environmental drivers of the dominant/nondominant disparity. We found different assembly patterns for dominants and nondominants, consistent with asymmetries in assembly mechanisms. Among the different postulated mechanisms, our results suggest two complementary hypotheses seldom explored: (1) Nondominant species include lineages adapted to thrive in the environment generated by dominant species. (2) Even when dominant species reduce resources to nondominant ones, dominant species could have a stronger positive effect on some nondominants by ameliorating environmental stressors affecting them, than by depleting resources and increasing the environmental stress to those nondominants. These results show that the dominant/nondominant asymmetry has ecological and evolutionary consequences fundamental to understand plant communities. John Wiley and Sons Inc. 2021-11-22 /pmc/articles/PMC8717298/ /pubmed/35003636 http://dx.doi.org/10.1002/ece3.8266 Text en © 2021 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Arnillas, Carlos Alberto
Borer, Elizabeth T.
Seabloom, Eric W.
Alberti, Juan
Baez, Selene
Bakker, Jonathan D.
Boughton, Elizabeth H.
Buckley, Yvonne M.
Bugalho, Miguel Nuno
Donohue, Ian
Dwyer, John
Firn, Jennifer
Gridzak, Riley
Hagenah, Nicole
Hautier, Yann
Helm, Aveliina
Jentsch, Anke
Knops, Johannes M. H.
Komatsu, Kimberly J.
Laanisto, Lauri
Laungani, Ramesh
McCulley, Rebecca
Moore, Joslin L.
Morgan, John W.
Peri, Pablo Luis
Power, Sally A.
Price, Jodi
Sankaran, Mahesh
Schamp, Brandon
Speziale, Karina
Standish, Rachel
Virtanen, Risto
Cadotte, Marc W.
Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title_full Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title_fullStr Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title_full_unstemmed Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title_short Opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
title_sort opposing community assembly patterns for dominant and nondominant plant species in herbaceous ecosystems globally
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717298/
https://www.ncbi.nlm.nih.gov/pubmed/35003636
http://dx.doi.org/10.1002/ece3.8266
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