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Resource‐dependent antagonistic coevolution leads to a new paradox of enrichment
The classical, ecological, paradox of enrichment describes a phenomenon that resource enrichment destabilizes predator–prey systems by exacerbating population oscillations. Here we suggest a new, evolutionary, paradox of enrichment. Resource enrichment can lead to more asymmetrical predator–prey coe...
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Published in: | Ecology (Durham) 2016-05, Vol.97 (5), p.1319-1328 |
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creator | Zhang, Quan-Guo Buckling, Angus |
description | The classical, ecological, paradox of enrichment describes a phenomenon that resource enrichment destabilizes predator–prey systems by exacerbating population oscillations. Here we suggest a new, evolutionary, paradox of enrichment. Resource enrichment can lead to more asymmetrical predator–prey coevolution (i.e., extremely high levels of prey defenses against predators) that decreases predator abundances and increases predator extinction risk. A major reason for this is that high resource availability can reduce fitness costs associated with prey defenses. In our experiments with a bacterium and its lytic phage, nutrient‐balanced resource enrichment led to patterns in population demography and coevolutionary dynamics consistent with this coevolution‐based paradox of enrichment; in particular, phage population extinction events were observed under nutrient‐rich, not nutrient‐poor, conditions. Consistent with ecological studies, carbon‐biased resource enrichment (with carbon availability disproportionately increased relative to other nutrients) did not destabilize dynamics, and the asymmetry of coevolution was not altered in this context. Our work highlights the importance of integrating ecological and evolutionary thinking for studies of the consequences of nutrient pollution and other types of environmental changes. |
doi_str_mv | 10.1890/15-1408.1 |
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Our work highlights the importance of integrating ecological and evolutionary thinking for studies of the consequences of nutrient pollution and other types of environmental changes.</description><subject>adaptation</subject><subject>Adaptation, Physiological</subject><subject>Biological Evolution</subject><subject>Carbon - metabolism</subject><subject>coevolution</subject><subject>Ecology</subject><subject>environmental change</subject><subject>Evolutionary biology</subject><subject>experimental evolution</subject><subject>Extinction</subject><subject>Models, Biological</subject><subject>Nutrients</subject><subject>Pollution</subject><subject>Predation</subject><subject>predator–prey interactions</subject><subject>Pseudomonas fluorescens - genetics</subject><subject>Pseudomonas fluorescens - physiology</subject><subject>Pseudomonas Phages - genetics</subject><subject>Pseudomonas Phages - physiology</subject><subject>resource enrichment</subject><subject>stoichiometry</subject><subject>Time Factors</subject><subject>virus</subject><issn>0012-9658</issn><issn>1939-9170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkc9u1DAQhy0EotvCgQcALHGBQxaP_yT2Ea1aQKqEVOiBk-Uk45JV1l7shNIbj8Az8iR4lQISEhI-jA_-5hvbP0IeAVuDNuwlqAok02u4Q1ZghKkMNOwuWTEGvDK10kfkOOctKwukvk-OeCNMzcCsyMUF5jinDn98-97jHkOPYaIuTO4qhiFPQ0e7iF_iOE9DDHRE12c6RepowGu6d8n18SuNnmJIQ_dpV7ofkHvejRkf3u4n5PLs9MPmTXX-7vXbzavzqlPlGlXrgENruHPcs7rzpXjRMq8dbzrBa6lrLlDxVgvDEZ0Q2NZGC9kq3zjQ4oQ8X7z7FD_PmCe7G3KH4-gCxjlb0OygKOV_UCGlZMYU9Nlf6Lb8TygPsdAYroxquCrUi4XqUsw5obf7NOxcurHA7CETC8oeMrFQ2Ce3xrndYf-b_BVCAdYLcD2MePNvkz3dfAShZGl4vDRs8xTTH6FsmNDsIHy6nHsXrbtKQ7aX7zmDuuTfSFEG_wRKTqZ6</recordid><startdate>201605</startdate><enddate>201605</enddate><creator>Zhang, Quan-Guo</creator><creator>Buckling, Angus</creator><general>Brooklyn Botanical Garden</general><general>ECOLOGICAL SOCIETY OF AMERICA</general><general>Ecological Society of America</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7TV</scope></search><sort><creationdate>201605</creationdate><title>Resource‐dependent antagonistic coevolution leads to a new paradox of enrichment</title><author>Zhang, Quan-Guo ; Buckling, Angus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5014-ba121b92aa2f06cff06f3b0f8a27c32648623e52b8392eea33eb69834b5f7a183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adaptation</topic><topic>Adaptation, Physiological</topic><topic>Biological Evolution</topic><topic>Carbon - metabolism</topic><topic>coevolution</topic><topic>Ecology</topic><topic>environmental change</topic><topic>Evolutionary biology</topic><topic>experimental evolution</topic><topic>Extinction</topic><topic>Models, Biological</topic><topic>Nutrients</topic><topic>Pollution</topic><topic>Predation</topic><topic>predator–prey interactions</topic><topic>Pseudomonas fluorescens - genetics</topic><topic>Pseudomonas fluorescens - physiology</topic><topic>Pseudomonas Phages - genetics</topic><topic>Pseudomonas Phages - physiology</topic><topic>resource enrichment</topic><topic>stoichiometry</topic><topic>Time Factors</topic><topic>virus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Quan-Guo</creatorcontrib><creatorcontrib>Buckling, Angus</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Pollution Abstracts</collection><jtitle>Ecology (Durham)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Quan-Guo</au><au>Buckling, Angus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Resource‐dependent antagonistic coevolution leads to a new paradox of enrichment</atitle><jtitle>Ecology (Durham)</jtitle><addtitle>Ecology</addtitle><date>2016-05</date><risdate>2016</risdate><volume>97</volume><issue>5</issue><spage>1319</spage><epage>1328</epage><pages>1319-1328</pages><issn>0012-9658</issn><eissn>1939-9170</eissn><coden>ECGYAQ</coden><abstract>The classical, ecological, paradox of enrichment describes a phenomenon that resource enrichment destabilizes predator–prey systems by exacerbating population oscillations. Here we suggest a new, evolutionary, paradox of enrichment. Resource enrichment can lead to more asymmetrical predator–prey coevolution (i.e., extremely high levels of prey defenses against predators) that decreases predator abundances and increases predator extinction risk. A major reason for this is that high resource availability can reduce fitness costs associated with prey defenses. In our experiments with a bacterium and its lytic phage, nutrient‐balanced resource enrichment led to patterns in population demography and coevolutionary dynamics consistent with this coevolution‐based paradox of enrichment; in particular, phage population extinction events were observed under nutrient‐rich, not nutrient‐poor, conditions. Consistent with ecological studies, carbon‐biased resource enrichment (with carbon availability disproportionately increased relative to other nutrients) did not destabilize dynamics, and the asymmetry of coevolution was not altered in this context. Our work highlights the importance of integrating ecological and evolutionary thinking for studies of the consequences of nutrient pollution and other types of environmental changes.</abstract><cop>United States</cop><pub>Brooklyn Botanical Garden</pub><pmid>27396019</pmid><doi>10.1890/15-1408.1</doi><tpages>10</tpages></addata></record> |
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subjects | adaptation Adaptation, Physiological Biological Evolution Carbon - metabolism coevolution Ecology environmental change Evolutionary biology experimental evolution Extinction Models, Biological Nutrients Pollution Predation predator–prey interactions Pseudomonas fluorescens - genetics Pseudomonas fluorescens - physiology Pseudomonas Phages - genetics Pseudomonas Phages - physiology resource enrichment stoichiometry Time Factors virus |
title | Resource‐dependent antagonistic coevolution leads to a new paradox of enrichment |
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