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  4. Behavioral and genomic consequences of evolution under skewed sex ratios

Behavioral and genomic consequences of evolution under skewed sex ratios

File(s)
Modanu_cornellgrad_0058F_11856.pdf (2.1 MB)
Permanent Link(s)
https://doi.org/10.7298/r7b2-ea79
https://hdl.handle.net/1813/70131
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Cornell Theses and Dissertations
Author
Modanu, Maria
Abstract

In this dissertation I combine game theoretic modeling with experimental evolution and next-generation sequencing to address the causes and consequences of male and female sexual interactions. In chapter 1, I use tug-of-war theory to model the evolution of male and female sex roles as a function of anisogamy and sex ratio, and show that individuals can diverge in how they allocate their reproductive effort based on either of these parameters. The model incorporates both within-sex competition and between-sex cooperation to demonstrate that sexual interactions underlie the evolution of sexually dimorphic behaviors. In chapter 2, I perform experimental evolution in the laboratory using a nematode with a short generation time, Caenorhabditis remanei, and test an extension of the hypothesis that disrupting male-female interactions has cascading effects on reproductive behavior and gamete investment. By systematically altering the adult sex ratio of replicate populations over 50 generations, I show that males and females increase their mating effort when exposed to a population with an excess of males, but find no effects on their sperm and egg sizes. Chapter 3 extends this experiment by applying a genomic lens to this organism and exploring the consequences of a skewed sex ratio on populations, along with the potential for repeatable evolution in replicate populations faced with identical environmental conditions. I show that populations with a male-biased sex ratio tend towards higher genomic divergence compared to female-biased populations, and that parallel evolution can arise across experimental populations regardless of sex ratio, with implications for the predictability of evolutionary trajectories at short evolutionary timescales. Furthermore, I identify loci that change in allele frequency in opposite directions in male-biased and female-biased populations and are implicated in male mating behavior, indicating possible genes under sexual conflict in this system.

Description
113 pages
Date Issued
2019-12
Keywords
Caenorhabditis
•
experimental evolution
•
game theory
•
parallel evolution
•
sex role
•
sexual conflict
Committee Chair
Reeve, Hudson Kern
Committee Member
Shaw, Kerry L.
Dickinson, Janis Lou
Webster, Michael
Degree Discipline
Neurobiology and Behavior
Degree Name
Ph. D., Neurobiology and Behavior
Degree Level
Doctor of Philosophy
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International
Rights URI
https://creativecommons.org/licenses/by-nc-nd/4.0/
Type
dissertation or thesis
Link(s) to Catalog Record
https://newcatalog.library.cornell.edu/catalog/13119716

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