Seed parasitism redirects ovule development in Douglas fir

Many parasitic species of insects complete their entire development in seeds. They feed off storage reserves within the ovule. These reserves only normally accumulate in fertilized ovules. Consequently, female insects that oviposit their eggs directly into the plant ovule need to be able to select c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proceedings of the Royal Society. B, Biological sciences Biological sciences, 2005-07, Vol.272 (1571), p.1491-1496
Hauptverfasser: Von Aderkas, P, Rouault, G, Wagner, R, Rohr, R, Roques, A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1496
container_issue 1571
container_start_page 1491
container_title Proceedings of the Royal Society. B, Biological sciences
container_volume 272
creator Von Aderkas, P
Rouault, G
Wagner, R
Rohr, R
Roques, A
description Many parasitic species of insects complete their entire development in seeds. They feed off storage reserves within the ovule. These reserves only normally accumulate in fertilized ovules. Consequently, female insects that oviposit their eggs directly into the plant ovule need to be able to select correctly, as unfertilized ovules of conifers normally become so-called empty seed. We provide clear evidence that in conifers, seed-parasitizing insects do not need to discriminate between fertilized and unfertilized plant ovules when ovipositing their eggs. A host-specific insect, the chalcid Megastigmus spermotrophus Wachtl (Hymenoptera: Torymidae), lays its eggs in ovules of Douglas fir (Pseudotsuga menziesii (Mirbel) Franco) before fertilization has taken place in the plant. Oviposition not only prevents the expected degeneration and death of unfertilized ovules, but it induces energy reserve accumulation. Ovules that would otherwise develop as empty seed are redirected in their development by the insect to provide food for the developing larvae. Instead of the insect exploiting normal events during seed development, the insect manipulates seed development for its own reproductive advantage.
doi_str_mv 10.1098/rspb.2005.3061
format Article
fullrecord <record><control><sourceid>jstor_royal</sourceid><recordid>TN_cdi_royalsociety_journals_10_1098_rspb_2005_3061</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>30047712</jstor_id><sourcerecordid>30047712</sourcerecordid><originalsourceid>FETCH-LOGICAL-c781t-47abaf5259895206880d88ba8b799a78e9a4fcd190d782baa0dc0d00e229e7de3</originalsourceid><addsrcrecordid>eNqFUs9v0zAUjhCIjcGVG5ATEoeWZyeO7R0QY2MMqRKIsorbk5M4rbu0DnZSKH89blMVCmKcLPt9P957n6PoMYEhASleOt_kQwrAhglk5E50TFJOBlSy9G50DDKjA5EyehQ98H4OAJIJdj86IhkQIml6HJ2OtS7jRjnlTWv8Ina6NE4XrY_tqqt1XOqVrm2z0Ms2Nsv4wnbTWvm4Mu5hdK9StdePdudJdH359vP51WD04d3787PRoOCCtIOUq1xVjDIpJKOQCQGlELkSOZdScaGlSquiJBJKLmiuFJQFlACaUql5qZOT6FWv23T5QpdF6MSpGhtnFsqt0SqDh5WlmeHUrpCw4EllEHjRC8z-oF2djXDzBpRxgJSuSMA-35k5-7XTvsWF8YWua7XUtvOYiQBm9P9AwhkwyTfuwx5YOOu909W-BQK4yRA3GeImQ9xkGAhPf5_3F3wXWgAkPcDZdVi8LYxu1zi3nVuG679lb25jfRp_fLOinBrCOEEQCQFGJMnwh2l2Upyi8b7TuIUcyv_t9qR3m_vWuv0MSVgz54SG-qCvG9_q7_u6cjeY8YQznIgULy5HfEQnX3AS8K93GZrp7Fv4oXgwxta9sMs2fIFto9sWSSoJVl0dUi-rIEFvlbDrxvn8kB1Iz3pSpSyqqTMer8cUSAIEUgiJJD8Bt2MW4g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17505979</pqid></control><display><type>article</type><title>Seed parasitism redirects ovule development in Douglas fir</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>PubMed Central</source><creator>Von Aderkas, P ; Rouault, G ; Wagner, R ; Rohr, R ; Roques, A</creator><creatorcontrib>Von Aderkas, P ; Rouault, G ; Wagner, R ; Rohr, R ; Roques, A</creatorcontrib><description>Many parasitic species of insects complete their entire development in seeds. They feed off storage reserves within the ovule. These reserves only normally accumulate in fertilized ovules. Consequently, female insects that oviposit their eggs directly into the plant ovule need to be able to select correctly, as unfertilized ovules of conifers normally become so-called empty seed. We provide clear evidence that in conifers, seed-parasitizing insects do not need to discriminate between fertilized and unfertilized plant ovules when ovipositing their eggs. A host-specific insect, the chalcid Megastigmus spermotrophus Wachtl (Hymenoptera: Torymidae), lays its eggs in ovules of Douglas fir (Pseudotsuga menziesii (Mirbel) Franco) before fertilization has taken place in the plant. Oviposition not only prevents the expected degeneration and death of unfertilized ovules, but it induces energy reserve accumulation. Ovules that would otherwise develop as empty seed are redirected in their development by the insect to provide food for the developing larvae. Instead of the insect exploiting normal events during seed development, the insect manipulates seed development for its own reproductive advantage.</description><identifier>ISSN: 0962-8452</identifier><identifier>EISSN: 1471-2954</identifier><identifier>DOI: 10.1098/rspb.2005.3061</identifier><identifier>PMID: 16011924</identifier><language>eng</language><publisher>London: The Royal Society</publisher><subject>Animals ; British Columbia ; conifers ; Female ; France ; Host-Parasite Interactions ; Hymenoptera ; Insect development ; Insect eggs ; Insect larvae ; Insect reproduction ; Larval development ; Life Sciences ; Megastigmus ; Megastigmus spermotrophus ; Ova ; Oviposition ; Oviposition - physiology ; Ovules ; Parasitism ; parasitoids ; plant development ; plant-insect relations ; Plants ; Pseudotsuga ; Pseudotsuga - growth &amp; development ; Pseudotsuga - parasitology ; Pseudotsuga menziesii ; Seed Development ; Seed Parasite ; seeds ; Seeds - cytology ; Seeds - growth &amp; development ; Seeds - parasitology ; Symbiosis ; Torymidae ; Vespidae ; Wasps - physiology</subject><ispartof>Proceedings of the Royal Society. B, Biological sciences, 2005-07, Vol.272 (1571), p.1491-1496</ispartof><rights>Copyright 2005 The Royal Society</rights><rights>2005 The Royal Society</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2005 The Royal Society 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c781t-47abaf5259895206880d88ba8b799a78e9a4fcd190d782baa0dc0d00e229e7de3</citedby><cites>FETCH-LOGICAL-c781t-47abaf5259895206880d88ba8b799a78e9a4fcd190d782baa0dc0d00e229e7de3</cites><orcidid>0000-0002-3734-3918</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30047712$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30047712$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16011924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-lyon1.hal.science/hal-02570042$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Von Aderkas, P</creatorcontrib><creatorcontrib>Rouault, G</creatorcontrib><creatorcontrib>Wagner, R</creatorcontrib><creatorcontrib>Rohr, R</creatorcontrib><creatorcontrib>Roques, A</creatorcontrib><title>Seed parasitism redirects ovule development in Douglas fir</title><title>Proceedings of the Royal Society. B, Biological sciences</title><addtitle>PROC R SOC B</addtitle><description>Many parasitic species of insects complete their entire development in seeds. They feed off storage reserves within the ovule. These reserves only normally accumulate in fertilized ovules. Consequently, female insects that oviposit their eggs directly into the plant ovule need to be able to select correctly, as unfertilized ovules of conifers normally become so-called empty seed. We provide clear evidence that in conifers, seed-parasitizing insects do not need to discriminate between fertilized and unfertilized plant ovules when ovipositing their eggs. A host-specific insect, the chalcid Megastigmus spermotrophus Wachtl (Hymenoptera: Torymidae), lays its eggs in ovules of Douglas fir (Pseudotsuga menziesii (Mirbel) Franco) before fertilization has taken place in the plant. Oviposition not only prevents the expected degeneration and death of unfertilized ovules, but it induces energy reserve accumulation. Ovules that would otherwise develop as empty seed are redirected in their development by the insect to provide food for the developing larvae. Instead of the insect exploiting normal events during seed development, the insect manipulates seed development for its own reproductive advantage.</description><subject>Animals</subject><subject>British Columbia</subject><subject>conifers</subject><subject>Female</subject><subject>France</subject><subject>Host-Parasite Interactions</subject><subject>Hymenoptera</subject><subject>Insect development</subject><subject>Insect eggs</subject><subject>Insect larvae</subject><subject>Insect reproduction</subject><subject>Larval development</subject><subject>Life Sciences</subject><subject>Megastigmus</subject><subject>Megastigmus spermotrophus</subject><subject>Ova</subject><subject>Oviposition</subject><subject>Oviposition - physiology</subject><subject>Ovules</subject><subject>Parasitism</subject><subject>parasitoids</subject><subject>plant development</subject><subject>plant-insect relations</subject><subject>Plants</subject><subject>Pseudotsuga</subject><subject>Pseudotsuga - growth &amp; development</subject><subject>Pseudotsuga - parasitology</subject><subject>Pseudotsuga menziesii</subject><subject>Seed Development</subject><subject>Seed Parasite</subject><subject>seeds</subject><subject>Seeds - cytology</subject><subject>Seeds - growth &amp; development</subject><subject>Seeds - parasitology</subject><subject>Symbiosis</subject><subject>Torymidae</subject><subject>Vespidae</subject><subject>Wasps - physiology</subject><issn>0962-8452</issn><issn>1471-2954</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUs9v0zAUjhCIjcGVG5ATEoeWZyeO7R0QY2MMqRKIsorbk5M4rbu0DnZSKH89blMVCmKcLPt9P957n6PoMYEhASleOt_kQwrAhglk5E50TFJOBlSy9G50DDKjA5EyehQ98H4OAJIJdj86IhkQIml6HJ2OtS7jRjnlTWv8Ina6NE4XrY_tqqt1XOqVrm2z0Ms2Nsv4wnbTWvm4Mu5hdK9StdePdudJdH359vP51WD04d3787PRoOCCtIOUq1xVjDIpJKOQCQGlELkSOZdScaGlSquiJBJKLmiuFJQFlACaUql5qZOT6FWv23T5QpdF6MSpGhtnFsqt0SqDh5WlmeHUrpCw4EllEHjRC8z-oF2djXDzBpRxgJSuSMA-35k5-7XTvsWF8YWua7XUtvOYiQBm9P9AwhkwyTfuwx5YOOu909W-BQK4yRA3GeImQ9xkGAhPf5_3F3wXWgAkPcDZdVi8LYxu1zi3nVuG679lb25jfRp_fLOinBrCOEEQCQFGJMnwh2l2Upyi8b7TuIUcyv_t9qR3m_vWuv0MSVgz54SG-qCvG9_q7_u6cjeY8YQznIgULy5HfEQnX3AS8K93GZrp7Fv4oXgwxta9sMs2fIFto9sWSSoJVl0dUi-rIEFvlbDrxvn8kB1Iz3pSpSyqqTMer8cUSAIEUgiJJD8Bt2MW4g</recordid><startdate>20050722</startdate><enddate>20050722</enddate><creator>Von Aderkas, P</creator><creator>Rouault, G</creator><creator>Wagner, R</creator><creator>Rohr, R</creator><creator>Roques, A</creator><general>The Royal Society</general><general>Royal Society, The</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>C1K</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3734-3918</orcidid></search><sort><creationdate>20050722</creationdate><title>Seed parasitism redirects ovule development in Douglas fir</title><author>Von Aderkas, P ; Rouault, G ; Wagner, R ; Rohr, R ; Roques, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c781t-47abaf5259895206880d88ba8b799a78e9a4fcd190d782baa0dc0d00e229e7de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>British Columbia</topic><topic>conifers</topic><topic>Female</topic><topic>France</topic><topic>Host-Parasite Interactions</topic><topic>Hymenoptera</topic><topic>Insect development</topic><topic>Insect eggs</topic><topic>Insect larvae</topic><topic>Insect reproduction</topic><topic>Larval development</topic><topic>Life Sciences</topic><topic>Megastigmus</topic><topic>Megastigmus spermotrophus</topic><topic>Ova</topic><topic>Oviposition</topic><topic>Oviposition - physiology</topic><topic>Ovules</topic><topic>Parasitism</topic><topic>parasitoids</topic><topic>plant development</topic><topic>plant-insect relations</topic><topic>Plants</topic><topic>Pseudotsuga</topic><topic>Pseudotsuga - growth &amp; development</topic><topic>Pseudotsuga - parasitology</topic><topic>Pseudotsuga menziesii</topic><topic>Seed Development</topic><topic>Seed Parasite</topic><topic>seeds</topic><topic>Seeds - cytology</topic><topic>Seeds - growth &amp; development</topic><topic>Seeds - parasitology</topic><topic>Symbiosis</topic><topic>Torymidae</topic><topic>Vespidae</topic><topic>Wasps - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Von Aderkas, P</creatorcontrib><creatorcontrib>Rouault, G</creatorcontrib><creatorcontrib>Wagner, R</creatorcontrib><creatorcontrib>Rohr, R</creatorcontrib><creatorcontrib>Roques, A</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>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the Royal Society. B, Biological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Von Aderkas, P</au><au>Rouault, G</au><au>Wagner, R</au><au>Rohr, R</au><au>Roques, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Seed parasitism redirects ovule development in Douglas fir</atitle><jtitle>Proceedings of the Royal Society. B, Biological sciences</jtitle><addtitle>PROC R SOC B</addtitle><date>2005-07-22</date><risdate>2005</risdate><volume>272</volume><issue>1571</issue><spage>1491</spage><epage>1496</epage><pages>1491-1496</pages><issn>0962-8452</issn><eissn>1471-2954</eissn><abstract>Many parasitic species of insects complete their entire development in seeds. They feed off storage reserves within the ovule. These reserves only normally accumulate in fertilized ovules. Consequently, female insects that oviposit their eggs directly into the plant ovule need to be able to select correctly, as unfertilized ovules of conifers normally become so-called empty seed. We provide clear evidence that in conifers, seed-parasitizing insects do not need to discriminate between fertilized and unfertilized plant ovules when ovipositing their eggs. A host-specific insect, the chalcid Megastigmus spermotrophus Wachtl (Hymenoptera: Torymidae), lays its eggs in ovules of Douglas fir (Pseudotsuga menziesii (Mirbel) Franco) before fertilization has taken place in the plant. Oviposition not only prevents the expected degeneration and death of unfertilized ovules, but it induces energy reserve accumulation. Ovules that would otherwise develop as empty seed are redirected in their development by the insect to provide food for the developing larvae. Instead of the insect exploiting normal events during seed development, the insect manipulates seed development for its own reproductive advantage.</abstract><cop>London</cop><pub>The Royal Society</pub><pmid>16011924</pmid><doi>10.1098/rspb.2005.3061</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-3734-3918</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0962-8452
ispartof Proceedings of the Royal Society. B, Biological sciences, 2005-07, Vol.272 (1571), p.1491-1496
issn 0962-8452
1471-2954
language eng
recordid cdi_royalsociety_journals_10_1098_rspb_2005_3061
source MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central
subjects Animals
British Columbia
conifers
Female
France
Host-Parasite Interactions
Hymenoptera
Insect development
Insect eggs
Insect larvae
Insect reproduction
Larval development
Life Sciences
Megastigmus
Megastigmus spermotrophus
Ova
Oviposition
Oviposition - physiology
Ovules
Parasitism
parasitoids
plant development
plant-insect relations
Plants
Pseudotsuga
Pseudotsuga - growth & development
Pseudotsuga - parasitology
Pseudotsuga menziesii
Seed Development
Seed Parasite
seeds
Seeds - cytology
Seeds - growth & development
Seeds - parasitology
Symbiosis
Torymidae
Vespidae
Wasps - physiology
title Seed parasitism redirects ovule development in Douglas fir
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T01%3A05%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_royal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Seed%20parasitism%20redirects%20ovule%20development%20in%20Douglas%20fir&rft.jtitle=Proceedings%20of%20the%20Royal%20Society.%20B,%20Biological%20sciences&rft.au=Von%20Aderkas,%20P&rft.date=2005-07-22&rft.volume=272&rft.issue=1571&rft.spage=1491&rft.epage=1496&rft.pages=1491-1496&rft.issn=0962-8452&rft.eissn=1471-2954&rft_id=info:doi/10.1098/rspb.2005.3061&rft_dat=%3Cjstor_royal%3E30047712%3C/jstor_royal%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17505979&rft_id=info:pmid/16011924&rft_jstor_id=30047712&rfr_iscdi=true