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Title page for ETD etd-07272010-155621


Type of Document Dissertation
Author Janson, Eric Michael
URN etd-07272010-155621
Title The evolutionary ecology of an insect-fungus interaction: Botryosphaeria dothidea, symbiotic with the goldenrod-galling midge Asteromyia carbonifera (Diptera: Cecidomyiidae)
Degree PhD
Department Biological Sciences
Advisory Committee
Advisor Name Title
David E. McCauley Committee Chair
Daniel J. Funk Committee Member
John O. Stireman III Committee Member
Patrick Abbot Committee Member
Keywords
  • phenotypic complexity
  • phenotypic variation
  • symbiosis
  • plant-insect interaction
  • gall midge
  • microbial association
  • plant gall
  • fungus
Date of Defense 2010-03-26
Availability unrestricted
Abstract
Arguably, the process of adaptive ecological speciation and radiation has been the most important mechanism in contributing to the world’s immense biological diversity. Initial theoretical treatments of adaptive speciation made special mention of species interactions, namely interspecific competition, as an important source of divergent natural selection that ultimately contributed to the formation of novel ecological and species diversity. However, accumulating evidence suggests that mutualistic associations, especially those between microbes and insects, may be important in the process of adaptive speciation, as mutualists can act as sources of important phenotypic variation. In this dissertation, I investigate aspects of the interaction between the goldenrod-galling midge, Asteromyia carbonifera, and its fungal symbiont, Botryosphaeria dothidea, and attempt to relate the findings to ongoing evolutionary diversification within the species. First, a verbal theoretical treatment of how microbial mutualists could affect the process of adaptive speciation is put forth, using insects and their diverse microbial associates as examples. Second, I show by sterol-profile analysis that A. carbonifera appears to feed exclusively on its fungal associate, which may be important in opening nutritional ecological opportunity. Finally, I show that while the fungal associate mediates the observed phenotypic variation in gall morphology, it is the midge itself that is directly responsible for the ecologically important phenotypic variation. Moreover, the fungal associate does not exhibit the typical evolutionary signatures of a heritable mutualism. These data suggest that, for Asteromyia carbonifera, the fungal symbiont may indeed be a crucial player in the ongoing evolutionary radiation of its host, but the association does not appear to be a typical host-symbiont coevolutionary interaction.
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