Developmental plasticity in the queen-polymorphic ant Temnothorax longispinosus
Females of social Hymenoptera show developmental plasticity in response to varying social and environmental conditions, though some species have strong genetic influences on the form of the female reproductives. In ants, a queen polymorphism can occur in which large queens initiate new colonies on t...
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description | Females of social Hymenoptera show developmental plasticity in response to varying social and environmental conditions, though some species have strong genetic influences on the form of the female reproductives. In ants, a queen polymorphism can occur in which large queens initiate new colonies on their own, while small queens enter established nests. Most queen polymorphisms studied to date originate due to genetic differences between individuals of differing form. Here, we report on the development of female form in response to social factors within the nest in the queen-polymorphic ant
Temnothorax longispinosus
. Three queen size morphs occur: a rare large queen with higher fat stores that can found new colonies independently, a large queen that has low fat stores and is behaviorally flexible, and a small queen that rejoins the natal nest. Both in nesting units collected from the field and those reared in the lab, queen presence during larval development led to fewer larvae developing as gynes (virgin, winged queens), and most of those gynes were the small morph. This queen effect is transferred to developing gyne larvae by close, physical interaction between queens and workers, and causes slower larval development. We conclude that gyne size, and therefore reproductive behavior, in
T. longispinosus
is developmentally plastic in response to queen presence. Plasticity in reproductive behavior may be an adaptive response to the nest sites utilized by this species.
T. longispinosus
nests predominantly in acorns and hickory nuts, which can vary dramatically from 1 year to the next. Since queens are more likely to be present in each nesting unit when fewer nest sites are available, the queen effect that results in more small gynes produced links the expression of colony-founding traits to ecological conditions across habitat patches. |
doi_str_mv | 10.1007/s00040-013-0281-y |
format | Article |
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Temnothorax longispinosus
. Three queen size morphs occur: a rare large queen with higher fat stores that can found new colonies independently, a large queen that has low fat stores and is behaviorally flexible, and a small queen that rejoins the natal nest. Both in nesting units collected from the field and those reared in the lab, queen presence during larval development led to fewer larvae developing as gynes (virgin, winged queens), and most of those gynes were the small morph. This queen effect is transferred to developing gyne larvae by close, physical interaction between queens and workers, and causes slower larval development. We conclude that gyne size, and therefore reproductive behavior, in
T. longispinosus
is developmentally plastic in response to queen presence. Plasticity in reproductive behavior may be an adaptive response to the nest sites utilized by this species.
T. longispinosus
nests predominantly in acorns and hickory nuts, which can vary dramatically from 1 year to the next. Since queens are more likely to be present in each nesting unit when fewer nest sites are available, the queen effect that results in more small gynes produced links the expression of colony-founding traits to ecological conditions across habitat patches.</description><identifier>ISSN: 0020-1812</identifier><identifier>EISSN: 1420-9098</identifier><identifier>DOI: 10.1007/s00040-013-0281-y</identifier><language>eng</language><publisher>Basel: SP Birkhäuser Verlag Basel</publisher><subject>Animal and plant ecology ; Animal, plant and microbial ecology ; Animals ; Biological and medical sciences ; Biomedical and Life Sciences ; Demecology ; Entomology ; Formicidae ; Fundamental and applied biological sciences. Psychology ; Hymenoptera ; Life Sciences ; Protozoa. Invertebrata ; Research Article</subject><ispartof>Insectes sociaux, 2013-05, Vol.60 (2), p.179-189</ispartof><rights>International Union for the Study of Social Insects (IUSSI) 2013</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-adb0c1baf2cea91c0d24ab2ad8f0a44ed37572912dd75ef63c08419b549429943</citedby><cites>FETCH-LOGICAL-c351t-adb0c1baf2cea91c0d24ab2ad8f0a44ed37572912dd75ef63c08419b549429943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00040-013-0281-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00040-013-0281-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27933,27934,41497,42566,51328</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27233464$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Howard, K. J.</creatorcontrib><creatorcontrib>Jeanne, R. L.</creatorcontrib><title>Developmental plasticity in the queen-polymorphic ant Temnothorax longispinosus</title><title>Insectes sociaux</title><addtitle>Insect. Soc</addtitle><description>Females of social Hymenoptera show developmental plasticity in response to varying social and environmental conditions, though some species have strong genetic influences on the form of the female reproductives. In ants, a queen polymorphism can occur in which large queens initiate new colonies on their own, while small queens enter established nests. Most queen polymorphisms studied to date originate due to genetic differences between individuals of differing form. Here, we report on the development of female form in response to social factors within the nest in the queen-polymorphic ant
Temnothorax longispinosus
. Three queen size morphs occur: a rare large queen with higher fat stores that can found new colonies independently, a large queen that has low fat stores and is behaviorally flexible, and a small queen that rejoins the natal nest. Both in nesting units collected from the field and those reared in the lab, queen presence during larval development led to fewer larvae developing as gynes (virgin, winged queens), and most of those gynes were the small morph. This queen effect is transferred to developing gyne larvae by close, physical interaction between queens and workers, and causes slower larval development. We conclude that gyne size, and therefore reproductive behavior, in
T. longispinosus
is developmentally plastic in response to queen presence. Plasticity in reproductive behavior may be an adaptive response to the nest sites utilized by this species.
T. longispinosus
nests predominantly in acorns and hickory nuts, which can vary dramatically from 1 year to the next. Since queens are more likely to be present in each nesting unit when fewer nest sites are available, the queen effect that results in more small gynes produced links the expression of colony-founding traits to ecological conditions across habitat patches.</description><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Demecology</subject><subject>Entomology</subject><subject>Formicidae</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hymenoptera</subject><subject>Life Sciences</subject><subject>Protozoa. Invertebrata</subject><subject>Research Article</subject><issn>0020-1812</issn><issn>1420-9098</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EEqXwAeyyQWITGD_y8BKVp1Spm7K2HMdpXTl2sBNE_p5ErViympHmzNHMRegWwwMGKB4jADBIAdMUSInT8QwtMCOQcuDlOVoATD0uMblEVzEeJrokBV6gzbP-1tZ3rXa9tElnZeyNMv2YGJf0e518DVq7tPN2bH3o9kYl0vXJVrfO93sf5E9ivduZ2Bnn4xCv0UUjbdQ3p7pEn68v29V7ut68faye1qmiGe5TWVegcCUborTkWEFNmKyIrMsGJGO6pkVWEI5JXReZbnKqoGSYVxnjjHDO6BLdH71d8NOJsRetiUpbK532QxSYZjmnOStnFB9RFXyMQTeiC6aVYRQYxByeOIYnpvDEHJ4Yp527k15GJW0TpFMm_i2SglDK8tlNjlycRm6ngzj4Ibjp83_kv1h4gPI</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Howard, K. J.</creator><creator>Jeanne, R. L.</creator><general>SP Birkhäuser Verlag Basel</general><general>Birkhäuser</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>C1K</scope></search><sort><creationdate>20130501</creationdate><title>Developmental plasticity in the queen-polymorphic ant Temnothorax longispinosus</title><author>Howard, K. J. ; Jeanne, R. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-adb0c1baf2cea91c0d24ab2ad8f0a44ed37572912dd75ef63c08419b549429943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Demecology</topic><topic>Entomology</topic><topic>Formicidae</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hymenoptera</topic><topic>Life Sciences</topic><topic>Protozoa. Invertebrata</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Howard, K. J.</creatorcontrib><creatorcontrib>Jeanne, R. L.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Insectes sociaux</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Howard, K. J.</au><au>Jeanne, R. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental plasticity in the queen-polymorphic ant Temnothorax longispinosus</atitle><jtitle>Insectes sociaux</jtitle><stitle>Insect. Soc</stitle><date>2013-05-01</date><risdate>2013</risdate><volume>60</volume><issue>2</issue><spage>179</spage><epage>189</epage><pages>179-189</pages><issn>0020-1812</issn><eissn>1420-9098</eissn><abstract>Females of social Hymenoptera show developmental plasticity in response to varying social and environmental conditions, though some species have strong genetic influences on the form of the female reproductives. In ants, a queen polymorphism can occur in which large queens initiate new colonies on their own, while small queens enter established nests. Most queen polymorphisms studied to date originate due to genetic differences between individuals of differing form. Here, we report on the development of female form in response to social factors within the nest in the queen-polymorphic ant
Temnothorax longispinosus
. Three queen size morphs occur: a rare large queen with higher fat stores that can found new colonies independently, a large queen that has low fat stores and is behaviorally flexible, and a small queen that rejoins the natal nest. Both in nesting units collected from the field and those reared in the lab, queen presence during larval development led to fewer larvae developing as gynes (virgin, winged queens), and most of those gynes were the small morph. This queen effect is transferred to developing gyne larvae by close, physical interaction between queens and workers, and causes slower larval development. We conclude that gyne size, and therefore reproductive behavior, in
T. longispinosus
is developmentally plastic in response to queen presence. Plasticity in reproductive behavior may be an adaptive response to the nest sites utilized by this species.
T. longispinosus
nests predominantly in acorns and hickory nuts, which can vary dramatically from 1 year to the next. Since queens are more likely to be present in each nesting unit when fewer nest sites are available, the queen effect that results in more small gynes produced links the expression of colony-founding traits to ecological conditions across habitat patches.</abstract><cop>Basel</cop><pub>SP Birkhäuser Verlag Basel</pub><doi>10.1007/s00040-013-0281-y</doi><tpages>11</tpages></addata></record> |
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source | SpringerNature Journals |
subjects | Animal and plant ecology Animal, plant and microbial ecology Animals Biological and medical sciences Biomedical and Life Sciences Demecology Entomology Formicidae Fundamental and applied biological sciences. Psychology Hymenoptera Life Sciences Protozoa. Invertebrata Research Article |
title | Developmental plasticity in the queen-polymorphic ant Temnothorax longispinosus |
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