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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

Evolution of colour variation and species richness in agamid lizards /

Stuart-Fox, Devi M. January 2002 (has links) (PDF)
Thesis (Ph. D.)--University of Queensland, 2003. / Includes bibliographical references.
2

Evolutionary and ecological dynamics of aposematism and mimicry in poison frogs

Darst, Catherine Rachel, 1978- 10 August 2011 (has links)
Not available / text
3

Algal preferences in the masking behaviour of the spider crab, Notomithrax ursus : a thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Ecology, University of Canterbury /

Ertel, Catherine M. January 2008 (has links)
Thesis (M. Sc.)--University of Canterbury, 2008. / Typescript (photocopy). Includes bibliographical references (leaves 85-86). Also available via the World Wide.
4

Evolutionary and ecological dynamics of aposematism and mimicry in poison frogs

Darst, Catherine Rachel, January 1900 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 2006. / Vita. Includes bibliographical references.
5

Physiological and psychological aspects of flatfish camouflage.

Saidel, William Mark January 1978 (has links)
Thesis. 1978. Ph.D.--Massachusetts Institute of Technology. Dept. of Biology. / MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE. / Vita. / Bibliography : leaves 137-151. / Ph.D.
6

Functional aspects of behavior and morphology in the decorator crab Microphrys Bicornutus (Latreille, 1825) (Crustacea: Brachyura: Mithracidae)

Unknown Date (has links)
Masking or decorator crabs, conceal themselves partially through camouflage, by selecting or indiscriminately attaching materials from their environment to their exoskeleton. Functional aspects of decorating behavior and morphology in this group have not been documented. Using Microphrys bicornutus as a model species, this dissertation demonstrates clearly that decorating is an advantageous phenotype that has evolved to serve several functions. Decorating is a complex behavior that begins when a crab approaches an algal substrate and results in the attachment of algae to hooked setae on the exoskeleton. Once decorated, crabs remain motionless on the substrate until disturbed or until another behavior is initiated. This was confirmed for M. bicornutus, as crabs spent a significant amount of time feeding, remaining motionless, picking, and walking when compared to decorating. Crabs displayed agonistic behaviors during encounters with conspecifics conspecifics. These included both active aggressive behavior and display behavior. Crabs showed a decrease in motility during these encounters, helping maintain dispersed distributions, thereby decreasing intrsapecific encounters in the field. Trials were done to determine the effect of conspecifics, predators and feeding preferences on algal utilization. M. bicornutus showed a significant decrease in the amount of algae used for decoration in the highest density trials (i.e., 4 and 8 crabs). Agonistic displays and aggressive behavior between these crabs likely affected the time available for decorating. Decorated crabs isolated from an algal substrate were more likely to survive in the presence of either of two sympatric fish predators. Thus, being protected by the algal decoration on their exoskeletons. Trials also showed a parallel between algal consumption and algal materials used for decoration. In addition to its protective function, algae used by M. bicornutus for decoration simultaneously serve as short term food supplies for the crabs. Eleven morphologically complex structures were identified and mapped on the exoskeleton. Hooked setae were the primary structures used to attach algae to the crab’s body. Ten additional setal structures were present, including two novel types of setae. On the basis of location and morphological variation exhibited among these latter structures, a primary sensory function may be inferred. / Includes bibliography. / Dissertation (Ph.D.)--Florida Atlantic University, 2013.
7

Approche de formation continue en science et technologie du premier cycle du secondaire /

Routhier, Gilles, January 2006 (has links)
Thèse (M.Ed.) -- Université du Québec à Chicoutimi, 2006. / Bibliogr.: f. [96]-101. Document électronique également accessible en format PDF. CaQCU
8

Dispersion in camouflaged animals and searching image in predators (or, Searching image in the Carrion crow and some anti-predator adaptations in camouflaged prey)

Croze, Harvey January 1967 (has links)
No description available.
9

Survival value of the white coloration of gulls and other sea birds

Phillips, Graham C. January 1962 (has links)
No description available.
10

Differences in Sexual Dimorphism and Influences of Sexual Dichromatism on Crypsis Among Populations of the Jumping Spider Habronattus oregonensis

Bazzano, Jason 01 January 2011 (has links)
Crypsis can be an important mechanism of predator avoidance for organisms. However, many species exhibit sexual dichromatism, in which the males possess a suite of colorations in order to attract female attention. The resulting differences in crypsis between the males and females can provide insight into the relative strengths of the sexually and naturally selective forces shaping the coloration of the organism, as well as clues regarding potential sensory biases of the selecting sex. In this study, I examine variation in the coloration of four Pacific Northwest populations of the sexually dimorphic and dichromatic polygynous species of jumping spider Habronattus oregonensis and compare the coloration of different body regions of the spiders to their habitats. I also investigate differences in relative size of a male sexual ornament, the enlarged first leg tibia. Field work for this study was conducted in June and July of 2009. The three main foci of this study are 1) to compare the degree of color matching of females and their habitat to the degree of color matching of males and their habitat, evaluating whether sexual selection on males has reduced their degree of crypsis relative to that of females, 2) if there is indeed a difference in crypsis between the sexes, to gauge whether there are similar divergences from crypsis among the populations - both in the quantitative amount of divergences as well as the colorimetric direction of such divergences, and 3) whether there is any variation in sexual ornament size among populations. Male first leg tibia size is a sexual character that is presumably not influenced by habitat coloration; differences in male tibia allometry among populations would provide supporting evidence for the hypothesis that sexual selection is indeed maintaining phenotypic differences among the populations, regardless of habitat location and color. I found a high degree of conformity of hue and chroma between male and female spiders and their habitats, with three notable exceptions. The most extreme difference in coloration between spider and habitat was that of the Gorge and Siskiyou population male anteriors. The anteriors had proportionally less green and more ultraviolet reflectance than their habitat. Second, the Mt. Hood and Tillamook population male abdomens diverged from their habitat in a similar, although less pronounced manner to that of the Gorge and Siskiyou population male anteriors: they had proportionally less green and more UV reflectance. Third, female abdomens of all populations were highly variable in chroma, despite having hues that generally matched their habitat. Tibia area relative to body size of Gorge and Siskiyou population males was significantly smaller than that of Mt. Hood and Tillamook population males. The lower level of background hue matching among males compared to females implies that sexual selection has directly conflicted with natural selection, resulting in impaired crypsis. While the reduced crypsis of the Gorge and Siskiyou population males is centered on their anterior (the primary body region presented to the females during courtship), the deviations from crypsis in the Mt. Hood and Tillamook population males are highest on their abdomen, although the degree of contrast is lower than that of the Gorge and Siskiyou population anteriors. These differences in coloration between the Mt. Hood and Tillamook population male abdomens and their habitats are in the same colorimetric direction as those of the Gorge and Siskiyou population anteriors and their habitat; this may indicate a sensory bias of the females, conserved in all four populations, selecting for male reflectance with a higher UV to green ratio. The fact that Mt. Hood and Tillamook population male abdomens have a more modest reduction in background matching compared to Gorge and Siskiyou population male anteriors may be due to the search methods of flying predators (e.g., spider wasps); the dorsum would presumably be more conspicuous to predators than the anterior, and would thus be subject to more intense selection for crypsis despite sexual selection to the contrary. The variability of abdomen coloration of females of both morphs may indicate that selection for crypsis is less strong among females than among males. One possible reason for this would be if females spent less time in the exposed courtship habitat than males, a conclusion implied by a highly male-skewed sex ratio encountered during field collections. Like the differences in coloration between different males of different populations, the significant differences in male tibia size also imply variability in the intensity of sexual selection. Relative importance of male coloration and tibia size may be weighted differently among populations, operating under similar constraints on reductions in survival accrued by developing these characters. The high degree of variation found among the populations implies that there is a degree of reproductive isolation among the chromatically and morphologically dissimilar populations. However, the similarity of the environments in which the populations existed, the close geographic proximity of some of the dissimilar populations, and the lack of any substantial geographic boundaries between the populations imply that this isolation is not maintained through extrinsic factors. Rather, it would seem that the interpopulational diversity is maintained by sexual selection. However, evidence from morphology and coloration suggest that the generation of this diversity is not evolving exclusively under sexual selection pressure, but rather is constrained to a degree by natural selection.

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