Calling Behavior and Sex Pheromone Release and Storage in the Moth Chloridea virescens
Female moths release sex pheromone to attract mates. In most species, sex pheromone is produced in, and released from, a specific gland. In a previous study, we used empirical data and compartmental modeling to account for the major pheromone gland processes of female Chloridea virescens : synthesis...
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description | Female moths release sex pheromone to attract mates. In most species, sex pheromone is produced in, and released from, a specific gland. In a previous study, we used empirical data and compartmental modeling to account for the major pheromone gland processes of female
Chloridea virescens
: synthesis, storage, catabolism and release; we found that females released little (20–30%) of their pheromone, with most catabolized. The recent publication of a new pheromone collection method led us to reinvestigate pheromone release and catabolism in
C. virescens
on the basis that our original study might have underestimated release rate (thereby overestimating catabolism) due to methodology and females not calling (releasing) continuously. Further we wished to compare pheromone storage/catabolism between calling and non-calling females. First, we observed calling intermittency of females. Then, using decapitated females, we used the new collection method, along with compartmental modeling, gland sampling and stable isotope labeling, to determine differences in pheromone release, catabolism and storage between (forced) simulated calling and non-calling females. We found, (i) intact 1 d females call intermittently; (ii) pheromone is released at a higher rate than previously determined, with simulations estimating that continuously calling females release ca. 70% of their pheromone (only 30% catabolized); (iii) extension (calling)/retraction of the ovipositor is a highly effective “on/off’ mechanism for release; (iv) both calling and non-calling females store most pheromone on or near the gland surface, but calling females catabolize less pheromone; (v) females are capable of producing and releasing pheromone very rapidly. Thus, not only is the moth pheromone gland efficient, in terms of the proportion of pheromone released Vs. catabolized, but it is highly effective at shutting on/off a high flux of pheromone for release. |
doi_str_mv | 10.1007/s10886-019-01133-w |
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Chloridea virescens
: synthesis, storage, catabolism and release; we found that females released little (20–30%) of their pheromone, with most catabolized. The recent publication of a new pheromone collection method led us to reinvestigate pheromone release and catabolism in
C. virescens
on the basis that our original study might have underestimated release rate (thereby overestimating catabolism) due to methodology and females not calling (releasing) continuously. Further we wished to compare pheromone storage/catabolism between calling and non-calling females. First, we observed calling intermittency of females. Then, using decapitated females, we used the new collection method, along with compartmental modeling, gland sampling and stable isotope labeling, to determine differences in pheromone release, catabolism and storage between (forced) simulated calling and non-calling females. We found, (i) intact 1 d females call intermittently; (ii) pheromone is released at a higher rate than previously determined, with simulations estimating that continuously calling females release ca. 70% of their pheromone (only 30% catabolized); (iii) extension (calling)/retraction of the ovipositor is a highly effective “on/off’ mechanism for release; (iv) both calling and non-calling females store most pheromone on or near the gland surface, but calling females catabolize less pheromone; (v) females are capable of producing and releasing pheromone very rapidly. Thus, not only is the moth pheromone gland efficient, in terms of the proportion of pheromone released Vs. catabolized, but it is highly effective at shutting on/off a high flux of pheromone for release.</description><identifier>ISSN: 0098-0331</identifier><identifier>EISSN: 1573-1561</identifier><identifier>DOI: 10.1007/s10886-019-01133-w</identifier><identifier>PMID: 31845137</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Agriculture ; Aldehydes - analysis ; Aldehydes - pharmacology ; Animals ; Biochemistry ; Biological Microscopy ; Biomedical and Life Sciences ; Butterflies & moths ; Calling behavior ; Carbon Isotopes - chemistry ; Catabolism ; Chloridea virescens ; Collection ; Computer simulation ; Ecology ; Entomology ; Female ; Females ; Gas Chromatography-Mass Spectrometry ; Glucose - chemistry ; Glucose - metabolism ; Isotope Labeling ; Life Sciences ; Male ; Modelling ; Moths - physiology ; Ovipositor ; Pheromone gland ; Pheromones ; Reproductive Biology ; Scent Glands - metabolism ; Sex ; Sex Attractants - analysis ; Sex Attractants - metabolism ; Sex Attractants - pharmacology ; Sex pheromone ; Sexual behavior ; Sexual Behavior, Animal - drug effects ; Stable isotopes</subject><ispartof>Journal of chemical ecology, 2020, Vol.46 (1), p.10-20</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Journal of Chemical Ecology is a copyright of Springer, (2019). All Rights Reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-674ead9b4b15df3c0558b3e2cd0b0ff892d5fbad871257ddb02642225535e26c3</citedby><cites>FETCH-LOGICAL-c453t-674ead9b4b15df3c0558b3e2cd0b0ff892d5fbad871257ddb02642225535e26c3</cites><orcidid>0000-0003-4760-8390 ; 0000-0003-1666-295X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10886-019-01133-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10886-019-01133-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31845137$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02573248$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Foster, Stephen P.</creatorcontrib><creatorcontrib>Anderson, Karin G.</creatorcontrib><creatorcontrib>Casas, Jérôme</creatorcontrib><title>Calling Behavior and Sex Pheromone Release and Storage in the Moth Chloridea virescens</title><title>Journal of chemical ecology</title><addtitle>J Chem Ecol</addtitle><addtitle>J Chem Ecol</addtitle><description>Female moths release sex pheromone to attract mates. In most species, sex pheromone is produced in, and released from, a specific gland. In a previous study, we used empirical data and compartmental modeling to account for the major pheromone gland processes of female
Chloridea virescens
: synthesis, storage, catabolism and release; we found that females released little (20–30%) of their pheromone, with most catabolized. The recent publication of a new pheromone collection method led us to reinvestigate pheromone release and catabolism in
C. virescens
on the basis that our original study might have underestimated release rate (thereby overestimating catabolism) due to methodology and females not calling (releasing) continuously. Further we wished to compare pheromone storage/catabolism between calling and non-calling females. First, we observed calling intermittency of females. Then, using decapitated females, we used the new collection method, along with compartmental modeling, gland sampling and stable isotope labeling, to determine differences in pheromone release, catabolism and storage between (forced) simulated calling and non-calling females. We found, (i) intact 1 d females call intermittently; (ii) pheromone is released at a higher rate than previously determined, with simulations estimating that continuously calling females release ca. 70% of their pheromone (only 30% catabolized); (iii) extension (calling)/retraction of the ovipositor is a highly effective “on/off’ mechanism for release; (iv) both calling and non-calling females store most pheromone on or near the gland surface, but calling females catabolize less pheromone; (v) females are capable of producing and releasing pheromone very rapidly. Thus, not only is the moth pheromone gland efficient, in terms of the proportion of pheromone released Vs. catabolized, but it is highly effective at shutting on/off a high flux of pheromone for release.</description><subject>Agriculture</subject><subject>Aldehydes - analysis</subject><subject>Aldehydes - pharmacology</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biological Microscopy</subject><subject>Biomedical and Life Sciences</subject><subject>Butterflies & moths</subject><subject>Calling behavior</subject><subject>Carbon Isotopes - chemistry</subject><subject>Catabolism</subject><subject>Chloridea virescens</subject><subject>Collection</subject><subject>Computer simulation</subject><subject>Ecology</subject><subject>Entomology</subject><subject>Female</subject><subject>Females</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Glucose - chemistry</subject><subject>Glucose - metabolism</subject><subject>Isotope Labeling</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Modelling</subject><subject>Moths - physiology</subject><subject>Ovipositor</subject><subject>Pheromone gland</subject><subject>Pheromones</subject><subject>Reproductive Biology</subject><subject>Scent Glands - metabolism</subject><subject>Sex</subject><subject>Sex Attractants - analysis</subject><subject>Sex Attractants - metabolism</subject><subject>Sex Attractants - pharmacology</subject><subject>Sex pheromone</subject><subject>Sexual behavior</subject><subject>Sexual Behavior, Animal - drug effects</subject><subject>Stable isotopes</subject><issn>0098-0331</issn><issn>1573-1561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1v1DAQhi0EokvhD3BAlriUQ8qMPxLnWFaFIi0C8XW1nHiySZWNi53dwr_HJW2ROHCwRvI87zszehl7jnCKANXrhGBMWQDW-aGUxfUDtkJdyQJ1iQ_ZCqA2BUiJR-xJSpcAIEqjH7MjiUZplNWKfV-7cRymLX9DvTsMIXI3ef6FfvJPPcWwCxPxzzSSS7R05hDdlvgw8bkn_iHMPV_3Y4iDJ8cPQ6TU0pSeskedGxM9u63H7Nvb86_ri2Lz8d379dmmaJWWc1FWipyvG9Wg9p1sQWvTSBKthwa6ztTC665x3lQodOV9kw9QQgitpSZRtvKYvVp8ezfaqzjsXPxlgxvsxdnG3vxB1kmhzAEze7KwVzH82FOa7W7Iy46jmyjskxVSVLVCqOuMvvwHvQz7OOVLMqWEwrKsdKbEQrUxpBSpu98Awd4kZJeEbE7I_knIXmfRi1vrfbMjfy-5iyQDcgFSbk1bin9n_8f2N9nNmgQ</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Foster, Stephen P.</creator><creator>Anderson, Karin G.</creator><creator>Casas, Jérôme</creator><general>Springer US</general><general>Springer Nature B.V</general><general>Springer Verlag</general><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>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-4760-8390</orcidid><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid></search><sort><creationdate>2020</creationdate><title>Calling Behavior and Sex Pheromone Release and Storage in the Moth Chloridea virescens</title><author>Foster, Stephen P. ; Anderson, Karin G. ; Casas, Jérôme</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-674ead9b4b15df3c0558b3e2cd0b0ff892d5fbad871257ddb02642225535e26c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Agriculture</topic><topic>Aldehydes - 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pharmacology</topic><topic>Sex pheromone</topic><topic>Sexual behavior</topic><topic>Sexual Behavior, Animal - drug effects</topic><topic>Stable isotopes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Foster, Stephen P.</creatorcontrib><creatorcontrib>Anderson, Karin G.</creatorcontrib><creatorcontrib>Casas, Jérôme</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</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 Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of chemical ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Foster, Stephen P.</au><au>Anderson, Karin G.</au><au>Casas, Jérôme</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calling Behavior and Sex Pheromone Release and Storage in the Moth Chloridea virescens</atitle><jtitle>Journal of chemical ecology</jtitle><stitle>J Chem Ecol</stitle><addtitle>J Chem Ecol</addtitle><date>2020</date><risdate>2020</risdate><volume>46</volume><issue>1</issue><spage>10</spage><epage>20</epage><pages>10-20</pages><issn>0098-0331</issn><eissn>1573-1561</eissn><abstract>Female moths release sex pheromone to attract mates. In most species, sex pheromone is produced in, and released from, a specific gland. In a previous study, we used empirical data and compartmental modeling to account for the major pheromone gland processes of female
Chloridea virescens
: synthesis, storage, catabolism and release; we found that females released little (20–30%) of their pheromone, with most catabolized. The recent publication of a new pheromone collection method led us to reinvestigate pheromone release and catabolism in
C. virescens
on the basis that our original study might have underestimated release rate (thereby overestimating catabolism) due to methodology and females not calling (releasing) continuously. Further we wished to compare pheromone storage/catabolism between calling and non-calling females. First, we observed calling intermittency of females. Then, using decapitated females, we used the new collection method, along with compartmental modeling, gland sampling and stable isotope labeling, to determine differences in pheromone release, catabolism and storage between (forced) simulated calling and non-calling females. We found, (i) intact 1 d females call intermittently; (ii) pheromone is released at a higher rate than previously determined, with simulations estimating that continuously calling females release ca. 70% of their pheromone (only 30% catabolized); (iii) extension (calling)/retraction of the ovipositor is a highly effective “on/off’ mechanism for release; (iv) both calling and non-calling females store most pheromone on or near the gland surface, but calling females catabolize less pheromone; (v) females are capable of producing and releasing pheromone very rapidly. Thus, not only is the moth pheromone gland efficient, in terms of the proportion of pheromone released Vs. catabolized, but it is highly effective at shutting on/off a high flux of pheromone for release.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31845137</pmid><doi>10.1007/s10886-019-01133-w</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4760-8390</orcidid><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Agriculture Aldehydes - analysis Aldehydes - pharmacology Animals Biochemistry Biological Microscopy Biomedical and Life Sciences Butterflies & moths Calling behavior Carbon Isotopes - chemistry Catabolism Chloridea virescens Collection Computer simulation Ecology Entomology Female Females Gas Chromatography-Mass Spectrometry Glucose - chemistry Glucose - metabolism Isotope Labeling Life Sciences Male Modelling Moths - physiology Ovipositor Pheromone gland Pheromones Reproductive Biology Scent Glands - metabolism Sex Sex Attractants - analysis Sex Attractants - metabolism Sex Attractants - pharmacology Sex pheromone Sexual behavior Sexual Behavior, Animal - drug effects Stable isotopes |
title | Calling Behavior and Sex Pheromone Release and Storage in the Moth Chloridea virescens |
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