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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

ENZYME VARIABILITY IN NATURAL POPULATIONS OF TWO SPECIES OF CACTOPHILIC DROSOPHILA

Sluss, Elizabeth Susan, 1944- January 1975 (has links)
No description available.
2

Polymorphism at the H-2 locus in mice a test for heterozygote advantage due to maternal-fetal incompatibility /

Calderon, Javier. January 1980 (has links)
Thesis (M.S.)--University of Wisconsin--Madison. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 37-40).
3

An analysis of the maintenance and control of a polymorphism in the limpet Acmaea digitalis Eschscholtz

Giesel, James Theodore, 1941- 12 1900 (has links)
University of Oregon theses, Dept. of Biology, Ph.D., 1968. A print copy of this title is available from University of Oregon's Oregon Institute of Marine Biology library and at the Science library, under the call number: QL 430.4 .G5
4

Mitochondrial DNA polymorphism in American shad (Alosa sapidissima) and its implications for population structure

Bentzen, Paul January 1988 (has links)
Analysis of mitochondrial DNA (mtDNA) sequence variation among 244 American shad (Alosa sapidissima) from 14 rivers spanning the (Florida-Quebec) range of the species revealed several unusual features of shad mtDNA polymorphism. Two types of heteroplasmy, one involving a length polymorphism and the other a restriction site are common in shad. The length polymorphism involves a novel tandem triplication of a 1.5-kb sequence in the D-loop region. Both forms of heteroplasmy stem from multiple mutational events. The mtDNA data indicate that shad populations are reproductively discrete, and suggest that differences in the reproductive traits of northern and southern shad populations have evolved since the Pleistocene. Low mtDNA sequence variation in shad may stem at least in part from Pleistocene population reductions. A fossil calibration supports an mtDNA divergence rate in shad at least one order of magnitude slower than the prevailing estimate for vertebrates.
5

The role of thermal niche selection in the maintenance of a colour polymorphism in Plethodon cinereus

Petruzzi, Erin E. January 2005 (has links)
Thesis (M.S.)--University of Akron, Dept. of Biology, 2005. / "May, 2005." Title from electronic thesis title page (viewed 09/24/2005) Includes bibliographical references.
6

Mitochondrial DNA polymorphism in American shad (Alosa sapidissima) and its implications for population structure

Bentzen, Paul January 1988 (has links)
No description available.
7

Differential gene expression and the effects on molecular evolution and diversity /

Foxe, John Paul January 2007 (has links)
Thesis (M.A.)--York University, 2007. Graduate Programme in Biology. / Typescript. Includes bibliographical references (leaves 74-77). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:MR29562
8

Evolution and maintenance of plumage polymorphism the case of the red-footed booby (Sula sula) /

Baião, Patricia C. January 2008 (has links)
2 PDF files included one for title page and one for main document Title from title page PDF (University of Missouri--St. Louis, viewed February 8, 2010). Includes bibliographical references.
9

Investigating life-history polymorphism : modelling mites

Koesters, Nils B. January 2005 (has links)
The thesis presents research on the life-history polymorphism in the mite Sancassania berlesei. Males of this species are andropolymorphic: there are two distinct male phenotypes. One, the fighter, develops a third thickened leg pair, with which it kills off other fighters and males which do not exhibit a third thickened leg pair, the non-fighters. A review of the life-history of S. berlesei is given, focussing on its general biology, diet, dispersal and mating behaviour. This is followed by a review of the andropolymorphism, and the current understanding of the mechanisms underlying it. The major conclusions from the experimental work presented in this thesis are that fighters primarily develop at low population densities; though the proportion of males becoming fighters at any given density may change over time. This change is likely to be due to condition-dependence. Data is presented to illuminate these matters and a model is developed linking fighter development to the costs of being a fighter (in terms of survival) and the benefits of being a fighter (in terms of fecundity). The sex ratio in S. berlesei is 1:1, and there is no evidence of density or frequency-dependent deviations from this. A delay in food supply at maturation delays the time of maximum fecundity of females for about seven days and lowers their overall egg output. Density-dependent effects reduce the overall daily fecundity of females in higher densities. Female survival is affected by density, food present and rearing conditions. Nearly all eggs laid by S. berlesei hatch regardless of the conditions. Eggs laid in very poor conditions hatched even earlier than the average time of between day three and four. At density two, animals do synchronise their frequency, when isolated together from egg stage. Poor conditions reverse female density-dependence from convex to concave with the lowest life expectancy at intermediate densities. The trade-off between survival and fecundity is the likely cause. Amalgamating the results from the previous experiments, the influence of stochastic population dynamics on male strategy was then modelled. The results indicate that the fighter morph development rule is sensitive to the probability of low population densities arising. When low densities occur, there is a selective advantage to being a fighter. With increasing probability of lower densities, becoming a fighter is more feasible. The ESS rule changes, while in a stable high density environment a density-dependent fighter rule is never selected for. This indicates an influence of stochastic population dynamics on life-history evolution. Modelling demographic stochasticity in the fighter rule shows some buffering effect of this form of stochasticity. The fighter morph determination rule is less sensitive to environmental stochasticity with a high frequency of low densities. Using an agent based model with diploid genetics, I show that under high densities a fighter male is less successful at passing on his genes than a non-fighter. At a density of one male, the fighter gains no advantage to developing the fighter phenotype (as he is not competing with other males). In this case, the advantage may arise through future increases in density (such as through immigration or maturation of offspring). The density-dependent fighter development rule is then switched within the model from density-dependent to frequency-dependent, and the model indicates, that even under the frequency-dependent rule a possible ratio of fighters to non-fighters could exist. The system does not reach this state due to condition-dependence in reality. Following on from the findings discussed above, that morph determination has a condition-dependent component, I develop an argument that relates the observed forms of morph determination (density-dependent and frequency-dependent) in three closely related species of mites via an underlying condition-dependence. It is shown that condition-dependence is likely the linking factor between frequency and density-dependence. This is shown to be possibly a rule for all species displaying polymorphism which includes physical alterations of their bodies.
10

Evolution and genetics of colour polymorphism in three ladybird species

Michie, Laura Jane January 2011 (has links)
No description available.

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