Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern
Spatially explicit predator-prey interactions can alter the predatory potential of natural enemies augmented through conservation biological control. To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to s...
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Veröffentlicht in: | Molecular ecology 2008-04, Vol.17 (7), p.1828-1839 |
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creator | GRIFFITHS, GEORGIANNE J.K ALEXANDER, COLIN J HOLLAND, JOHN M KENNEDY, PETER J PERRY, JOE N SYMONDSON, WILLIAM O.C WINDER, LINTON |
description | Spatially explicit predator-prey interactions can alter the predatory potential of natural enemies augmented through conservation biological control. To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to study the foraging behaviour of a generalist carabid predator, Poecilus cupreus, in response to spatial patterns of its cereal aphid prey (Metapolophium dirhodum and Sitobion avenae). Beetle and aphid numbers were measured across two grids of sampling locations, within which aphid spatial pattern had been manipulated to generate patchy and more homogenous distributions. Aphid consumption was measured by enzyme-linked immunosorbent assays (ELISA) of beetle gut contents, using an aphid-specific monoclonal antibody. Movement and distribution patterns suggest that P. cupreus does not aggregate at, nor instigate prey-taxis within, aphid patches. However, more than two-thirds of the 2169 P. cupreus tested by ELISA had consumed aphids and the proportion of beetles containing aphid proteins was positively related to aphid density. Against expectation, the proportion of predators feeding on aphids was greatest where prey were homogenously distributed, and this was attributed to the loss of partial refuges for prey in aphid patches. The functional value of this type of uniform foraging strategy is ideally suited to early colonization of the crop habitat, when aphid numbers are low, before populations build up and form strong spatial patterns. |
doi_str_mv | 10.1111/j.1365-294X.2007.03682.x |
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To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to study the foraging behaviour of a generalist carabid predator, Poecilus cupreus, in response to spatial patterns of its cereal aphid prey (Metapolophium dirhodum and Sitobion avenae). Beetle and aphid numbers were measured across two grids of sampling locations, within which aphid spatial pattern had been manipulated to generate patchy and more homogenous distributions. Aphid consumption was measured by enzyme-linked immunosorbent assays (ELISA) of beetle gut contents, using an aphid-specific monoclonal antibody. Movement and distribution patterns suggest that P. cupreus does not aggregate at, nor instigate prey-taxis within, aphid patches. However, more than two-thirds of the 2169 P. cupreus tested by ELISA had consumed aphids and the proportion of beetles containing aphid proteins was positively related to aphid density. Against expectation, the proportion of predators feeding on aphids was greatest where prey were homogenously distributed, and this was attributed to the loss of partial refuges for prey in aphid patches. The functional value of this type of uniform foraging strategy is ideally suited to early colonization of the crop habitat, when aphid numbers are low, before populations build up and form strong spatial patterns.</description><identifier>ISSN: 0962-1083</identifier><identifier>EISSN: 1365-294X</identifier><identifier>DOI: 10.1111/j.1365-294X.2007.03682.x</identifier><identifier>PMID: 18284569</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>aggregation ; Animals ; Antibodies, Monoclonal - immunology ; Aphididae ; Aphids - physiology ; Coleoptera - physiology ; Conservation ; conservation biological control ; displacement ; Ecology ; ELISA ; Enzyme-Linked Immunosorbent Assay ; Gastrointestinal Contents ; Habitats ; Insects ; Molecular biology ; patch ; Poecilus cupreus ; Population Density ; Predation ; Predatory Behavior ; prey refuge ; Rhopalosiphum padi ; Sitobion avenae</subject><ispartof>Molecular ecology, 2008-04, Vol.17 (7), p.1828-1839</ispartof><rights>2008 The Authors. Journal compilation © 2008 Blackwell Publishing Ltd</rights><rights>Journal compilation © 2008 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4872-12e2be2d05199a952d6044e625f7df825d769ff1528b57b5b60c3325ae5a22233</citedby><cites>FETCH-LOGICAL-c4872-12e2be2d05199a952d6044e625f7df825d769ff1528b57b5b60c3325ae5a22233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-294X.2007.03682.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-294X.2007.03682.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18284569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GRIFFITHS, GEORGIANNE J.K</creatorcontrib><creatorcontrib>ALEXANDER, COLIN J</creatorcontrib><creatorcontrib>HOLLAND, JOHN M</creatorcontrib><creatorcontrib>KENNEDY, PETER J</creatorcontrib><creatorcontrib>PERRY, JOE N</creatorcontrib><creatorcontrib>SYMONDSON, WILLIAM O.C</creatorcontrib><creatorcontrib>WINDER, LINTON</creatorcontrib><title>Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern</title><title>Molecular ecology</title><addtitle>Mol Ecol</addtitle><description>Spatially explicit predator-prey interactions can alter the predatory potential of natural enemies augmented through conservation biological control. To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to study the foraging behaviour of a generalist carabid predator, Poecilus cupreus, in response to spatial patterns of its cereal aphid prey (Metapolophium dirhodum and Sitobion avenae). Beetle and aphid numbers were measured across two grids of sampling locations, within which aphid spatial pattern had been manipulated to generate patchy and more homogenous distributions. Aphid consumption was measured by enzyme-linked immunosorbent assays (ELISA) of beetle gut contents, using an aphid-specific monoclonal antibody. Movement and distribution patterns suggest that P. cupreus does not aggregate at, nor instigate prey-taxis within, aphid patches. However, more than two-thirds of the 2169 P. cupreus tested by ELISA had consumed aphids and the proportion of beetles containing aphid proteins was positively related to aphid density. Against expectation, the proportion of predators feeding on aphids was greatest where prey were homogenously distributed, and this was attributed to the loss of partial refuges for prey in aphid patches. The functional value of this type of uniform foraging strategy is ideally suited to early colonization of the crop habitat, when aphid numbers are low, before populations build up and form strong spatial patterns.</description><subject>aggregation</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Aphididae</subject><subject>Aphids - physiology</subject><subject>Coleoptera - physiology</subject><subject>Conservation</subject><subject>conservation biological control</subject><subject>displacement</subject><subject>Ecology</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Gastrointestinal Contents</subject><subject>Habitats</subject><subject>Insects</subject><subject>Molecular biology</subject><subject>patch</subject><subject>Poecilus cupreus</subject><subject>Population Density</subject><subject>Predation</subject><subject>Predatory Behavior</subject><subject>prey refuge</subject><subject>Rhopalosiphum padi</subject><subject>Sitobion avenae</subject><issn>0962-1083</issn><issn>1365-294X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhL0DEobcEexx_HTigVWmrfgCiC9wsJ3FaL9l4sbN099_XaVZF4gK-jO153rE9rxHKCC5IGu-WBaGc5aDKHwVgLApMuYRi-wTNHhNP0QwrDjnBkh6gFzEuMSYUGHuODogEWTKuZmhx6Xtfd743XWb6wVW-cTZmwf62aae-Nf1NWro-WwfbmMGHzLatq53t611254bbMbHL4toMLglSGGzoX6JnremifbWPh2jx8fh6fppffDo5m3-4yOtSinQ1sFBZaDAjShnFoOG4LC0H1oqmlcAawVXbEgayYqJiFcc1TU8wlhkAoPQQHU1118H_2tg46JWLte0601u_iVqkciC5_CdIFBWpIyyBb_8Cl34TUneiBoK5SqfzBMkJqoOPMdhWr4NbmbDTBOvRIL3Uow969EGPBukHg_Q2SV_v62-qlW3-CPeOJOD9BNy5zu7-u7C-PJ6Ps6TPJ72Lg90-6k34qbmggunvVyf6upyf8y_fPuuxM28mvjVem5vgol58hfRTMJZCSCXoPSpYtrs</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>GRIFFITHS, GEORGIANNE J.K</creator><creator>ALEXANDER, COLIN J</creator><creator>HOLLAND, JOHN M</creator><creator>KENNEDY, PETER J</creator><creator>PERRY, JOE N</creator><creator>SYMONDSON, WILLIAM O.C</creator><creator>WINDER, LINTON</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>BSCLL</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>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7QG</scope><scope>7ST</scope><scope>7U6</scope><scope>7X8</scope></search><sort><creationdate>200804</creationdate><title>Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern</title><author>GRIFFITHS, GEORGIANNE J.K ; ALEXANDER, COLIN J ; HOLLAND, JOHN M ; KENNEDY, PETER J ; PERRY, JOE N ; SYMONDSON, WILLIAM O.C ; WINDER, LINTON</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4872-12e2be2d05199a952d6044e625f7df825d769ff1528b57b5b60c3325ae5a22233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>aggregation</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Aphididae</topic><topic>Aphids - physiology</topic><topic>Coleoptera - physiology</topic><topic>Conservation</topic><topic>conservation biological control</topic><topic>displacement</topic><topic>Ecology</topic><topic>ELISA</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Gastrointestinal Contents</topic><topic>Habitats</topic><topic>Insects</topic><topic>Molecular biology</topic><topic>patch</topic><topic>Poecilus cupreus</topic><topic>Population Density</topic><topic>Predation</topic><topic>Predatory Behavior</topic><topic>prey refuge</topic><topic>Rhopalosiphum padi</topic><topic>Sitobion avenae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GRIFFITHS, GEORGIANNE J.K</creatorcontrib><creatorcontrib>ALEXANDER, COLIN J</creatorcontrib><creatorcontrib>HOLLAND, JOHN M</creatorcontrib><creatorcontrib>KENNEDY, PETER J</creatorcontrib><creatorcontrib>PERRY, JOE N</creatorcontrib><creatorcontrib>SYMONDSON, WILLIAM O.C</creatorcontrib><creatorcontrib>WINDER, LINTON</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Animal Behavior Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GRIFFITHS, GEORGIANNE J.K</au><au>ALEXANDER, COLIN J</au><au>HOLLAND, JOHN M</au><au>KENNEDY, PETER J</au><au>PERRY, JOE N</au><au>SYMONDSON, WILLIAM O.C</au><au>WINDER, LINTON</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern</atitle><jtitle>Molecular ecology</jtitle><addtitle>Mol Ecol</addtitle><date>2008-04</date><risdate>2008</risdate><volume>17</volume><issue>7</issue><spage>1828</spage><epage>1839</epage><pages>1828-1839</pages><issn>0962-1083</issn><eissn>1365-294X</eissn><abstract>Spatially explicit predator-prey interactions can alter the predatory potential of natural enemies augmented through conservation biological control. To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to study the foraging behaviour of a generalist carabid predator, Poecilus cupreus, in response to spatial patterns of its cereal aphid prey (Metapolophium dirhodum and Sitobion avenae). Beetle and aphid numbers were measured across two grids of sampling locations, within which aphid spatial pattern had been manipulated to generate patchy and more homogenous distributions. Aphid consumption was measured by enzyme-linked immunosorbent assays (ELISA) of beetle gut contents, using an aphid-specific monoclonal antibody. Movement and distribution patterns suggest that P. cupreus does not aggregate at, nor instigate prey-taxis within, aphid patches. However, more than two-thirds of the 2169 P. cupreus tested by ELISA had consumed aphids and the proportion of beetles containing aphid proteins was positively related to aphid density. Against expectation, the proportion of predators feeding on aphids was greatest where prey were homogenously distributed, and this was attributed to the loss of partial refuges for prey in aphid patches. The functional value of this type of uniform foraging strategy is ideally suited to early colonization of the crop habitat, when aphid numbers are low, before populations build up and form strong spatial patterns.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18284569</pmid><doi>10.1111/j.1365-294X.2007.03682.x</doi><tpages>12</tpages></addata></record> |
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subjects | aggregation Animals Antibodies, Monoclonal - immunology Aphididae Aphids - physiology Coleoptera - physiology Conservation conservation biological control displacement Ecology ELISA Enzyme-Linked Immunosorbent Assay Gastrointestinal Contents Habitats Insects Molecular biology patch Poecilus cupreus Population Density Predation Predatory Behavior prey refuge Rhopalosiphum padi Sitobion avenae |
title | Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern |
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