Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants
Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The “mother knows best” principle suggests that females prefer to oviposit on hosts that increase offspring survival. The “optim...
Gespeichert in:
Veröffentlicht in: | Ecology and evolution 2012-07, Vol.2 (7), p.1446-1457 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1457 |
---|---|
container_issue | 7 |
container_start_page | 1446 |
container_title | Ecology and evolution |
container_volume | 2 |
creator | García‐Robledo, Carlos Horvitz, Carol C. |
description | Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The “mother knows best” principle suggests that females prefer to oviposit on hosts that increase offspring survival. The “optimal bad motherhood” principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using a study system in which four Cephaloleia beetles are currently expanding their diets from native to exotic plants in the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive, or follow the patterns predicted by the “mother knows best” or the “optimal bad motherhood” principles. Interactions with novel hosts generated parent–offspring conflicts. Larval survival was higher on native hosts. However, adult generally lived longer on novel hosts. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the “mothers knows best” principle.
Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The "mother‐knows‐best" principle suggests that females prefer to oviposit on hosts that increase offspring survival. The "optimal‐bad‐motherhood" principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using as study system four Cephaloleia beetles currently expanding their |
doi_str_mv | 10.1002/ece3.267 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3434947</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1038614433</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4717-916b0ce8e9bed40c252995882a46908474c68f6915acfbdd734ec5325dd81d243</originalsourceid><addsrcrecordid>eNqFks1qFTEUxwex2NIWfAIJuHHRqfnOzEaQy_UDCrrQdcgkmd7UTDImc2-pq_sOLtzoy90nMcOttQpiCOQk58c_5xz-VfUYwXMEIX5utSXnmIsH1RGGlNVCsObhvfiwOs35CpbFIaZQPKoOMW6ZQIwcVd_eq2TDtNt-jX2fx-TCJdAx9N7pKZ-B3fZ7HCc3KA86ZcAQp5VNqxjNbvsDqGBAuc_QPgE-hXidQWfzNOdnNe1GbzNwoexs9QQK1rlNTOVRRx-D-zJ_GeLGerCKeQKjV2HKJ9VBr3y2p7fncfXx1fLD4k198e7128XLi1pTgUTdIt5BbRvbdtZQqDHDbcuaBivKW9hQQTVvet4ipnTfGSMItZoRzIxpkMGUHFcv9rrjuhus0WUWSXlZSh9UupFROflnJriVvIwbSSihLRVF4NmtQIqf16VzObisrS9d2LjOEgmEGceipf9HIWk4opSQgj79C72K6xTKJCSBXGCMGIO_BXWKOSfb39WNoJy9IWdvyOKNgj653-cd-MsJBaj3wLXz9uafQnK5WJJZ8Cfj08oT</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3067221550</pqid></control><display><type>article</type><title>Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants</title><source>Wiley Online Library - AutoHoldings Journals</source><source>PubMed Central Free</source><source>DOAJ Directory of Open Access Journals</source><source>Wiley Online Library Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>García‐Robledo, Carlos ; Horvitz, Carol C.</creator><creatorcontrib>García‐Robledo, Carlos ; Horvitz, Carol C.</creatorcontrib><description>Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The “mother knows best” principle suggests that females prefer to oviposit on hosts that increase offspring survival. The “optimal bad motherhood” principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using a study system in which four Cephaloleia beetles are currently expanding their diets from native to exotic plants in the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive, or follow the patterns predicted by the “mother knows best” or the “optimal bad motherhood” principles. Interactions with novel hosts generated parent–offspring conflicts. Larval survival was higher on native hosts. However, adult generally lived longer on novel hosts. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the “mothers knows best” principle.
Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The "mother‐knows‐best" principle suggests that females prefer to oviposit on hosts that increase offspring survival. The "optimal‐bad‐motherhood" principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using as study system four Cephaloleia beetles currently expanding their diets from native to exotic plants from the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive or follow the patterns predicted by the "mother‐knows‐best" or the "optimal‐bad‐motherhood" principles. Interactions with novel hosts generated parent‐offspring conflicts. Larval survival was higher on native hosts. However, adult longevity may increase on novel host plants. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the "mothers‐knows‐best" principle.</description><identifier>ISSN: 2045-7758</identifier><identifier>EISSN: 2045-7758</identifier><identifier>DOI: 10.1002/ece3.267</identifier><identifier>PMID: 22957153</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Beetles ; Cephaloleia ; Coleoptera ; Ecology ; Exotic plants ; Fecundity ; feeding preference ; Females ; Herbivores ; Host plants ; Insects ; Introduced plants ; larval and adult survival ; Natural selection ; Offspring ; Original Research ; Oviposition ; oviposition preference ; parent and offspring performance ; Phylogenetics ; Population growth ; Principles ; Specialization ; Survival ; Trends ; Zingiberales</subject><ispartof>Ecology and evolution, 2012-07, Vol.2 (7), p.1446-1457</ispartof><rights>2011 The Authors. published by Blackwell Publishing Ltd.</rights><rights>2012. This work is published under http://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 The Authors. Published by Blackwell Publishing Ltd. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4717-916b0ce8e9bed40c252995882a46908474c68f6915acfbdd734ec5325dd81d243</citedby><cites>FETCH-LOGICAL-c4717-916b0ce8e9bed40c252995882a46908474c68f6915acfbdd734ec5325dd81d243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434947/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434947/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22957153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García‐Robledo, Carlos</creatorcontrib><creatorcontrib>Horvitz, Carol C.</creatorcontrib><title>Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants</title><title>Ecology and evolution</title><addtitle>Ecol Evol</addtitle><description>Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The “mother knows best” principle suggests that females prefer to oviposit on hosts that increase offspring survival. The “optimal bad motherhood” principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using a study system in which four Cephaloleia beetles are currently expanding their diets from native to exotic plants in the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive, or follow the patterns predicted by the “mother knows best” or the “optimal bad motherhood” principles. Interactions with novel hosts generated parent–offspring conflicts. Larval survival was higher on native hosts. However, adult generally lived longer on novel hosts. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the “mothers knows best” principle.
Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The "mother‐knows‐best" principle suggests that females prefer to oviposit on hosts that increase offspring survival. The "optimal‐bad‐motherhood" principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using as study system four Cephaloleia beetles currently expanding their diets from native to exotic plants from the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive or follow the patterns predicted by the "mother‐knows‐best" or the "optimal‐bad‐motherhood" principles. Interactions with novel hosts generated parent‐offspring conflicts. Larval survival was higher on native hosts. However, adult longevity may increase on novel host plants. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the "mothers‐knows‐best" principle.</description><subject>Beetles</subject><subject>Cephaloleia</subject><subject>Coleoptera</subject><subject>Ecology</subject><subject>Exotic plants</subject><subject>Fecundity</subject><subject>feeding preference</subject><subject>Females</subject><subject>Herbivores</subject><subject>Host plants</subject><subject>Insects</subject><subject>Introduced plants</subject><subject>larval and adult survival</subject><subject>Natural selection</subject><subject>Offspring</subject><subject>Original Research</subject><subject>Oviposition</subject><subject>oviposition preference</subject><subject>parent and offspring performance</subject><subject>Phylogenetics</subject><subject>Population growth</subject><subject>Principles</subject><subject>Specialization</subject><subject>Survival</subject><subject>Trends</subject><subject>Zingiberales</subject><issn>2045-7758</issn><issn>2045-7758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFks1qFTEUxwex2NIWfAIJuHHRqfnOzEaQy_UDCrrQdcgkmd7UTDImc2-pq_sOLtzoy90nMcOttQpiCOQk58c_5xz-VfUYwXMEIX5utSXnmIsH1RGGlNVCsObhvfiwOs35CpbFIaZQPKoOMW6ZQIwcVd_eq2TDtNt-jX2fx-TCJdAx9N7pKZ-B3fZ7HCc3KA86ZcAQp5VNqxjNbvsDqGBAuc_QPgE-hXidQWfzNOdnNe1GbzNwoexs9QQK1rlNTOVRRx-D-zJ_GeLGerCKeQKjV2HKJ9VBr3y2p7fncfXx1fLD4k198e7128XLi1pTgUTdIt5BbRvbdtZQqDHDbcuaBivKW9hQQTVvet4ipnTfGSMItZoRzIxpkMGUHFcv9rrjuhus0WUWSXlZSh9UupFROflnJriVvIwbSSihLRVF4NmtQIqf16VzObisrS9d2LjOEgmEGceipf9HIWk4opSQgj79C72K6xTKJCSBXGCMGIO_BXWKOSfb39WNoJy9IWdvyOKNgj653-cd-MsJBaj3wLXz9uafQnK5WJJZ8Cfj08oT</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>García‐Robledo, Carlos</creator><creator>Horvitz, Carol C.</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7X2</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7U6</scope><scope>5PM</scope></search><sort><creationdate>201207</creationdate><title>Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants</title><author>García‐Robledo, Carlos ; Horvitz, Carol C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4717-916b0ce8e9bed40c252995882a46908474c68f6915acfbdd734ec5325dd81d243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Beetles</topic><topic>Cephaloleia</topic><topic>Coleoptera</topic><topic>Ecology</topic><topic>Exotic plants</topic><topic>Fecundity</topic><topic>feeding preference</topic><topic>Females</topic><topic>Herbivores</topic><topic>Host plants</topic><topic>Insects</topic><topic>Introduced plants</topic><topic>larval and adult survival</topic><topic>Natural selection</topic><topic>Offspring</topic><topic>Original Research</topic><topic>Oviposition</topic><topic>oviposition preference</topic><topic>parent and offspring performance</topic><topic>Phylogenetics</topic><topic>Population growth</topic><topic>Principles</topic><topic>Specialization</topic><topic>Survival</topic><topic>Trends</topic><topic>Zingiberales</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García‐Robledo, Carlos</creatorcontrib><creatorcontrib>Horvitz, Carol C.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Sustainability Science Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Ecology and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García‐Robledo, Carlos</au><au>Horvitz, Carol C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants</atitle><jtitle>Ecology and evolution</jtitle><addtitle>Ecol Evol</addtitle><date>2012-07</date><risdate>2012</risdate><volume>2</volume><issue>7</issue><spage>1446</spage><epage>1457</epage><pages>1446-1457</pages><issn>2045-7758</issn><eissn>2045-7758</eissn><abstract>Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The “mother knows best” principle suggests that females prefer to oviposit on hosts that increase offspring survival. The “optimal bad motherhood” principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using a study system in which four Cephaloleia beetles are currently expanding their diets from native to exotic plants in the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive, or follow the patterns predicted by the “mother knows best” or the “optimal bad motherhood” principles. Interactions with novel hosts generated parent–offspring conflicts. Larval survival was higher on native hosts. However, adult generally lived longer on novel hosts. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the “mothers knows best” principle.
Specialization of insect herbivores to one or a few host plants stimulated the development of two hypotheses on how natural selection should shape oviposition preferences: The "mother‐knows‐best" principle suggests that females prefer to oviposit on hosts that increase offspring survival. The "optimal‐bad‐motherhood" principle predicts that females prefer to oviposit on hosts that increase their own longevity. In insects colonizing novel host plants, current theory predicts that initial preferences of insect herbivores should be maladaptive, leading to ecological traps. Ecological trap theory does not take into account the fact that insect lineages frequently switch hosts at both ecological and evolutionary time scales. Therefore, the behavior of insect herbivores facing novel hosts is also shaped by natural selection. Using as study system four Cephaloleia beetles currently expanding their diets from native to exotic plants from the order Zingiberales, we determined if initial oviposition preferences are conservative, maladaptive or follow the patterns predicted by the "mother‐knows‐best" or the "optimal‐bad‐motherhood" principles. Interactions with novel hosts generated parent‐offspring conflicts. Larval survival was higher on native hosts. However, adult longevity may increase on novel host plants. In Cephaloleia beetles, oviposition preferences are usually associated with hosts that increase larval survival, female fecundity, and population growth. In most cases, Cephaloleia oviposition preferences follow the expectations of the "mothers‐knows‐best" principle.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22957153</pmid><doi>10.1002/ece3.267</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-7758 |
ispartof | Ecology and evolution, 2012-07, Vol.2 (7), p.1446-1457 |
issn | 2045-7758 2045-7758 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3434947 |
source | Wiley Online Library - AutoHoldings Journals; PubMed Central Free; DOAJ Directory of Open Access Journals; Wiley Online Library Open Access; EZB-FREE-00999 freely available EZB journals |
subjects | Beetles Cephaloleia Coleoptera Ecology Exotic plants Fecundity feeding preference Females Herbivores Host plants Insects Introduced plants larval and adult survival Natural selection Offspring Original Research Oviposition oviposition preference parent and offspring performance Phylogenetics Population growth Principles Specialization Survival Trends Zingiberales |
title | Parent–offspring conflicts, “optimal bad motherhood” and the “mother knows best” principles in insect herbivores colonizing novel host plants |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T04%3A57%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Parent%E2%80%93offspring%20conflicts,%20%E2%80%9Coptimal%20bad%20motherhood%E2%80%9D%20and%20the%20%E2%80%9Cmother%20knows%20best%E2%80%9D%20principles%20in%20insect%20herbivores%20colonizing%20novel%20host%20plants&rft.jtitle=Ecology%20and%20evolution&rft.au=Garc%C3%ADa%E2%80%90Robledo,%20Carlos&rft.date=2012-07&rft.volume=2&rft.issue=7&rft.spage=1446&rft.epage=1457&rft.pages=1446-1457&rft.issn=2045-7758&rft.eissn=2045-7758&rft_id=info:doi/10.1002/ece3.267&rft_dat=%3Cproquest_pubme%3E1038614433%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3067221550&rft_id=info:pmid/22957153&rfr_iscdi=true |