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Title page for ETD etd-12042006-101919


Type of Document Dissertation
Author Newcomb, James M
Author's Email Address jnewcomb@nec.edu
URN etd-12042006-101919
Title Homologous neurons and their locomotor functions in nudibranch molluscs
Degree Ph.D.
Department Biology
Advisory Committee
Advisor Name Title
Dr. Paul S. Katz Committee Chair
Dr. Charles D. Derby Committee Member
Dr. Dorothy H. Paul Committee Member
Dr. Ronald L. Calabrese Committee Member
Keywords
  • Serotonin
  • Homologous Neurons
  • Homology
  • Homoplasy
  • Invertebrate
  • Locomotion
  • Melibe
  • Mollusc
  • Nudibranch
  • Opisthobranch
  • Parallel Evolution
  • Phylogeny
  • Hermissenda
  • Gastropod
  • Evolution
  • Convergent Evolution
  • Divergent Evolution
  • Central Pattern Generator
  • Swimming
  • Tritonia
Date of Defense 2006-08-16
Availability unrestricted
Abstract
These studies compare neurotransmitter localization and the behavioral functions of homologous neurons in nudibranch molluscs to determine the types of changes that might underlie the evolution of species-specific behaviors. Serotonin (5-HT) immunohistochemistry in eleven nudibranch species indicated that certain groups of 5 HT-immunoreactive neurons, such as the Cerebral Serotonergic Posterior (CeSP) cluster, are present in all species. However, the locations and numbers of many other 5 HT-immunoreactive neurons were variable. Thus, particular parts of the serotonergic system have changed during the evolution of nudibranchs.

To test whether the functions of homologous neurons are phylogenetically variable, comparisons were made in species with divergent behaviors. In Tritonia diomedea, which crawls and also swims via dorsal-ventral body flexions, the CeSP cluster includes the Dorsal Swim Interneurons (DSIs). It was previously shown that the DSIs are members of the swim central pattern generator (CPG); they are rhythmically active during swimming and, along with their neurotransmitter 5-HT, are necessary and

sufficient for swimming. It was also known that the DSIs excite efferent neurons used in crawling. DSI homologues, the CeSP-A neurons, were identified in six species that do not exhibit dorsal-ventral swimming. Many physiological characteristics, including excitation of putative crawling neurons were conserved, but the CeSP A neurons were not rhythmically active in any of the six species. In the lateral flexion swimmer, Melibe leonina, the CeSP-A neurons and 5-HT, were sufficient, but not necessary, for swimming. Thus, homologous neurons, and their neurotransmitter, have functionally diverged in species with different behaviors.

Homologous neurons in species with similar behaviors also exhibited functional divergence. Like Melibe, Dendronotus iris is a lateral flexion swimmer. Swim interneuron 1 (Si1) is in the Melibe swim CPG. However, its putative homologue in Dendronotus, the Cerebral Posterior ipsilateral Pedal (CPiP) neuron, was not rhythmically active during swim-like motor patterns, but could initiate such a motor pattern. Together, these studies suggest that neurons have changed their functional relationships to neural circuits during the evolution of species-specific behaviors and have functionally diverged even in species that exhibit similar behaviors.

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