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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

An Investigation of Teneral Matings, Male Coercion, and Female Response. A Second Investigation of Caffeine Tolerance in Drosophila Melanogaster

Seeley, Corrine J. January 2010 (has links)
<p> Chapter 1-4 focuses on investigating whether forced copulations occur in teneral females, and how the female responds. There has only been one paper to report mating in newly eclosed (teneral) female matings in fruit flies (Drosophila melanogaster), and it was suggested to be forced. The focus of this thesis is to determine whether teneral matings are forced and how this may affect the future remating and reproductive success of females. Within the thesis, chapter 1 and 4 results suggest that teneral matings occur in both Canton-S and wild caught females, and occur in females less than 30 minutes post eclosion. Chapter 3 compared the male/female interaction of teneral females vs. immature females that successfully reject male mating attempts. Males were more aggressive with teneral females, and females displayed more rejection behaviours during courtship and mating. Chapter 4, was aimed at investigating what the reproductive consequences are, and results suggest that a teneral mating yields less progeny than a mature mating, and 68% of tenerally mated females remate at maturity.</p> <p> Chapter 5 and 6 focuses on investigating whether situational caffeine tolerance can be developed in fruit flies. Chapter 5 results indicate that caffeine causes a rest disruption, and a general tolerance to the rest disrupting effects can be gained over 6 days of repeated administration. The experiments in chapter 6 used various protocols to investigate whether a situational tolerance will develop, using odours and colours as associative cues. No conclusive results were found.</p> / Thesis / Master of Science (MSc)
2

Finite Subdivision Rules from Matings of Quadratic Functions: Existence and Constructions

Wilkerson, Mary 25 May 2012 (has links)
Combinatorial methods are utilized to examine preimage iterations of topologically glued polynomials. In particular, this paper addresses using finite subdivision rules and Hubbard trees as tools to model the dynamic behavior of mated quadratic functions. Several methods of construction of invariant structures on modified degenerate matings are detailed, and examples of parameter-based families of matings for which these methods succeed (and fail) are given. / Ph. D.
3

Two families of holomorphic correspondences

Curtis, Andrew January 2014 (has links)
Holomorphic correspondences are multivalued functions from the Riemann sphere to itself. This thesis is concerned with a certain type of holomorphic correspondence known as a covering correspondence. In particular we are concerned with a one complexdimensional family of correspondences constructed by post-composing a covering correspondence with a conformal involution. Correspondences constructed in this manner have varied and intricate dynamics. We introduce and analyze two subfamilies of this parameter space. The first family consists of correspondences for which the limit set is a Cantor set, the second family consists of correspondences for which the limit set is connected and for which the action of the correspondence on the complement of this limit set exhibits certain group like behaviour.
4

An analysis of a shared mating in V2.

Bjørnstad Pedersen, Lars January 2014 (has links)
In this master thesis we investigate, from a topological point of view and without applying Thurston´s Theorem, why the mating of the so called basilica polynomial <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D(z)=z%5E%7B2%7D-1" /> and the dendrite <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7Bi%7D(z)=z%5E%7B2%7D+i" /> is shared with the mating of <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D" /> and the dendrite <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-i%7D(z)=z%5E%7B2%7D-i" />. Both these matings equal the rational map <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?R_%7B3%7D(z)=%5Cfrac%7B3%7D%7Bz%5E%7B2%7D+2z%7D" />. Defined in the thesis are for both matings homeomorphic changes of coordinates<img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Cpsi_%7B-1%7D%5E%7B%5Cpm%7D" /> from the set <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?L=%5Coverset%7B%5Ccirc%7D%7BK%7D%5Cleft(f_%7B-1%7D%20%5Cright)%5Ccup%5Cleft(%5Ccup_%7Bn=0%7D%5E%7B%5Cinfty%7Df_%7B-1%7D%5E%7B%5Ccirc(-n)%7D(z_%7B%5Calpha%7D)%5Cright)" /> to the Fatou and Julia set of <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?R_%7B3%7D" />. Here <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?K%5Cleft(f_%7B-1%7D%20%5Cright)" /> is the filled Julia set of <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D" /> and <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?z_%7B%5Calpha%7D" /> is the <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Calpha" />-fixed point of <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?K%5Cleft(f_%7B-1%7D%20%5Cright)" />. / I detta examensarbete undersöker vi, från en topologisk synvinkel och utan applicering av Thurstons teorem, varför matchningen av det så kallade basilikapolynomet <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D(z)=z%5E%7B2%7D-1" /> och dendriten <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7Bi%7D(z)=z%5E%7B2%7D+i" /> är delad med matchningen av <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D" /> och dendriten <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-i%7D(z)=z%5E%7B2%7D-i" />. Båda dessa matchningar är lika med den rationella avbildningen  <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?R_%7B3%7D(z)=%5Cfrac%7B3%7D%7Bz%5E%7B2%7D+2z%7D" />. Definierat i examensarbetet är för båda matchningarna homoemorfa koordinatbyten<img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Cpsi_%7B-1%7D%5E%7B%5Cpm%7D" /> från mängden<img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?L=%5Coverset%7B%5Ccirc%7D%7BK%7D%5Cleft(f_%7B-1%7D%20%5Cright)%5Ccup%5Cleft(%5Ccup_%7Bn=0%7D%5E%7B%5Cinfty%7Df_%7B-1%7D%5E%7B%5Ccirc(-n)%7D(z_%7B%5Calpha%7D)%5Cright)" /> till Fatou- och Juliamängden av <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?R_%7B3%7D" />. Här är <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?K%5Cleft(f_%7B-1%7D%20%5Cright)" /> den ifyllda Juliamängden av avbildningen <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?f_%7B-1%7D" /> och <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?z_%7B%5Calpha%7D" /> är den <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?%5Calpha" />-fixerade punkten i <img src="http://www.diva-portal.org/cgi-bin/mimetex.cgi?K%5Cleft(f_%7B-1%7D%20%5Cright)" />.

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