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Dissecting the association between a gall midge, Asteromyia carbonifera, and its symbiotic fungus, Botryosphaeria dothidea
The Ambrosia gall midge [Asteromyia carbonifera (Osten Sacken) (Diptera: Cecidomyiidae: Alycaulini)] consists, in part, of a complex of genetically differentiated populations that have diverged in gall morphology on the host plant Solidago altissima L. (Asteraceae). This divergence appears to be an...
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Published in: | Entomologia experimentalis et applicata 2010-10, Vol.137 (1), p.36-49 |
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description | The Ambrosia gall midge [Asteromyia carbonifera (Osten Sacken) (Diptera: Cecidomyiidae: Alycaulini)] consists, in part, of a complex of genetically differentiated populations that have diverged in gall morphology on the host plant Solidago altissima L. (Asteraceae). This divergence appears to be an incipient adaptive radiation that may be driven by parasitoid pressure. Understanding the mechanisms driving this genetic and phenotypic diversification requires a close examination of the relationship between the midge and its fungal associate Botryosphaeria dothidea (Moug.) Ces. & De Not. (Ascomycota: Dothideomycetes), whose mycelia actually form the protective gall structure. We used manipulative experiments to test the degree of interdependency of the fungus and the midge, and we employed field and laboratory studies to gain insight into the source of fungal conidia, which our data and observations indicate are collected by females and stored in specialized pockets (mycangia) on the ovipositor. Manipulative experiments demonstrate that fungal proliferation on the host plant is dependent on the midge larvae and larvae exhibit significant growth on the fungus alone. Field observations and experiments were unable to identify the source of mycangial conidia; however, analyses of conidia shape suggest a biotrophic source. We conclude that this association is an obligatory mutualism with respect to successful gall formation. These findings corroborate recent findings that the primary food source of the midge is the gall fungus. |
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We used manipulative experiments to test the degree of interdependency of the fungus and the midge, and we employed field and laboratory studies to gain insight into the source of fungal conidia, which our data and observations indicate are collected by females and stored in specialized pockets (mycangia) on the ovipositor. Manipulative experiments demonstrate that fungal proliferation on the host plant is dependent on the midge larvae and larvae exhibit significant growth on the fungus alone. Field observations and experiments were unable to identify the source of mycangial conidia; however, analyses of conidia shape suggest a biotrophic source. We conclude that this association is an obligatory mutualism with respect to successful gall formation. 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III</creatorcontrib><title>Dissecting the association between a gall midge, Asteromyia carbonifera, and its symbiotic fungus, Botryosphaeria dothidea</title><title>Entomologia experimentalis et applicata</title><description>The Ambrosia gall midge [Asteromyia carbonifera (Osten Sacken) (Diptera: Cecidomyiidae: Alycaulini)] consists, in part, of a complex of genetically differentiated populations that have diverged in gall morphology on the host plant Solidago altissima L. (Asteraceae). This divergence appears to be an incipient adaptive radiation that may be driven by parasitoid pressure. Understanding the mechanisms driving this genetic and phenotypic diversification requires a close examination of the relationship between the midge and its fungal associate Botryosphaeria dothidea (Moug.) Ces. & De Not. (Ascomycota: Dothideomycetes), whose mycelia actually form the protective gall structure. We used manipulative experiments to test the degree of interdependency of the fungus and the midge, and we employed field and laboratory studies to gain insight into the source of fungal conidia, which our data and observations indicate are collected by females and stored in specialized pockets (mycangia) on the ovipositor. Manipulative experiments demonstrate that fungal proliferation on the host plant is dependent on the midge larvae and larvae exhibit significant growth on the fungus alone. Field observations and experiments were unable to identify the source of mycangial conidia; however, analyses of conidia shape suggest a biotrophic source. We conclude that this association is an obligatory mutualism with respect to successful gall formation. These findings corroborate recent findings that the primary food source of the midge is the gall fungus.</description><subject>adaptive radiation</subject><subject>Alycaulini</subject><subject>Ambrosia</subject><subject>Ambrosia gall</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Animals</subject><subject>Ascomycota</subject><subject>Asteraceae</subject><subject>Asteromyia carbonifera</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>Botryosphaeria dothidea</subject><subject>Cecidomyiidae</subject><subject>Diptera</subject><subject>Dothideomycetes</subject><subject>eclosion behaviour</subject><subject>ecological speciation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>microbial mutualism</subject><subject>Protozoa. Invertebrata</subject><subject>Solidago altissima</subject><subject>symbiosis</subject><subject>sympatry</subject><issn>0013-8703</issn><issn>1570-7458</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNkUGP1CAYhhujiePqb5CL8TIdoZTSHjyM47iu2ehh3Wj2Qr5S6DC2ZRaY7NRfL91u5iwJ4Qs8zwd5SRJE8IrE8WG_IozjlOesXGU47saZ49XpWbI4HzxPFhgTmpYc05fJK-_3GGPOK7JI_n423isZzNCisFMIvLfSQDB2QLUKD0oNCFALXYd607RqidY-KGf70QCS4Go7GK0cLBEMDTLBIz_2tbHBSKSPQ3v0S_TJBjdaf9iBctFqbNiZRsHr5IWGzqs3T-tFcvtl-3PzNb3-cXm1WV-nkjGKU4ZpoyuCSVMwlRGuG6AaWMHKhuac1bTWMteUUYlLVemK00LiArKcqKaoq5JeJO_nvgdn74_KB9EbL1XXwaDs0QteZBnPckojWc6kdNZ7p7Q4ONODGwXBYkpb7MUUqphCFVPa4jFtcYrqu6dLwEvotINBGn_2M0qqPEqR-zhzD6ZT43_3F9vteqqin86-id9wOvvg_oiCU87Er--Xori5u_v2O6vEJvJvZ16DFdC6-Kbbm9iZYlKWecYI_QeRCaxT</recordid><startdate>201010</startdate><enddate>201010</enddate><creator>Heath, Jeremy J</creator><creator>Stireman, John O. III</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope></search><sort><creationdate>201010</creationdate><title>Dissecting the association between a gall midge, Asteromyia carbonifera, and its symbiotic fungus, Botryosphaeria dothidea</title><author>Heath, Jeremy J ; Stireman, John O. III</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5530-503df9101d65e217fda3fa5658d3475b3bfc4f353c08e9f9736c06a241ed6b983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>adaptive radiation</topic><topic>Alycaulini</topic><topic>Ambrosia</topic><topic>Ambrosia gall</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Animals</topic><topic>Ascomycota</topic><topic>Asteraceae</topic><topic>Asteromyia carbonifera</topic><topic>Autoecology</topic><topic>Biological and medical sciences</topic><topic>Botryosphaeria dothidea</topic><topic>Cecidomyiidae</topic><topic>Diptera</topic><topic>Dothideomycetes</topic><topic>eclosion behaviour</topic><topic>ecological speciation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>microbial mutualism</topic><topic>Protozoa. Invertebrata</topic><topic>Solidago altissima</topic><topic>symbiosis</topic><topic>sympatry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heath, Jeremy J</creatorcontrib><creatorcontrib>Stireman, John O. III</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Entomologia experimentalis et applicata</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heath, Jeremy J</au><au>Stireman, John O. 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Understanding the mechanisms driving this genetic and phenotypic diversification requires a close examination of the relationship between the midge and its fungal associate Botryosphaeria dothidea (Moug.) Ces. & De Not. (Ascomycota: Dothideomycetes), whose mycelia actually form the protective gall structure. We used manipulative experiments to test the degree of interdependency of the fungus and the midge, and we employed field and laboratory studies to gain insight into the source of fungal conidia, which our data and observations indicate are collected by females and stored in specialized pockets (mycangia) on the ovipositor. Manipulative experiments demonstrate that fungal proliferation on the host plant is dependent on the midge larvae and larvae exhibit significant growth on the fungus alone. Field observations and experiments were unable to identify the source of mycangial conidia; however, analyses of conidia shape suggest a biotrophic source. We conclude that this association is an obligatory mutualism with respect to successful gall formation. These findings corroborate recent findings that the primary food source of the midge is the gall fungus.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><doi>10.1111/j.1570-7458.2010.01040.x</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adaptive radiation Alycaulini Ambrosia Ambrosia gall Animal and plant ecology Animal, plant and microbial ecology Animals Ascomycota Asteraceae Asteromyia carbonifera Autoecology Biological and medical sciences Botryosphaeria dothidea Cecidomyiidae Diptera Dothideomycetes eclosion behaviour ecological speciation Fundamental and applied biological sciences. Psychology microbial mutualism Protozoa. Invertebrata Solidago altissima symbiosis sympatry |
title | Dissecting the association between a gall midge, Asteromyia carbonifera, and its symbiotic fungus, Botryosphaeria dothidea |
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