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Thesis (PhD (Botany and Zoology))—University of Stellenbosch, 2009. / Females of many bird species prefer to mate with males exhibiting elaborate ornamentation, which serves as an indicator of male quality. Such ornaments, called secondary sexual traits, could act as signals to females that males could confer direct and/or indirect genetic benefits (when offspring inherit superior genes), on offspring. In particular, it has been suggested that these signals relate to male ability to resist infections, as only high quality individuals are able to invest both in high immune defence and elaborate ornament expression. The ostrich (Struthio camelus) is the largest living bird and is a member of the family of flightless birds, the ratites. They are sexually dimorphic, males displaying black plumage, and a pink-coloured neck and bill; whereas females display dull-brown plumage (both sexes have white feathers). Little is known about the mating system of ostriches: they are promiscuous and in the wild, males and females have multiple partners. The communal nesting system of ostriches is unique in that only the major female and major male provide parental care, in the form of incubation and guarding the offspring until independence. Furthermore, a remarkable feature of cohorts is that offspring may differ greatly in size, and these size differences are likely to have a genetic basis arising from differing parental genotypic differences. As a trade-off between immune response and life-history traits has been documented in various bird species, I examined the relationships between male secondary sexual traits (and specifically colouration) and maternal investment; levels of immunocompetence in both parents and chicks; and chick growth. This study showed that females invest more at the egg stage in response to traits involved in the male courtship display: the colour of the neck, white and black body feathers, and the brightness of black feathers. As these traits, which are exposed during the courtship display as well as during male-male interactions, were related to male immune responses, I suggest that only high quality males will be able to display their condition optimally. Chicks with higher growth rates were found to have intermediate responses to stimulation of their humoral immune system with diphtheria and tetanus vaccines, suggesting that not only fitness benefits, but also costs are associated with mounting an immune response; and that variation in humoral responses and growth rates relates to how individuals trade off these costs and benefits. In addition, chick humoral responses were found to be related to the humoral response of both parents, but through different antibody responses (maternal responses to tetanus and paternal responses to diphtheria), suggesting that this component of the immune system is heritable. As the colouration of white feathers predicted chick growth rates, as well as a male’s ability to raise an antibody response, I suggest that this visual cue could serve as a signal to females of male humoral immunocompetence, therefore forming the basis of mate choice whereby females could increase the fitness of their offspring through higher growth rates.

Long-tailed Manakins Chiroxiphia linearis are frugivorous birds with a lek mating system and male-male cooperation in courtship display. I studied male-male networks and correlates of male mating success in a color-banded population in Monteverde, Costa Rica, from 1981 to 1986. Males were organized in teams at scattered perch-zones (75 to 300 m apart) that were usually in aural but not visual contact. Each team consisted of 3 to 15 males (x=7.1±3.4), in an apparent linear dominance hierarchy, with an alpha and beta male who did most of the courtship display. In a study population with 50 to 60 active males per season, only 6 to 8 males were alphas. Only betas inherited alpha status (n=3). Males appear to be 8 or more years of age before attaining beta status. Alpha tenure can last 4 years. Alpha males were rarely or never seen in zones other than their 'home' zone. Lower-ranking males maintained simultaneous affiliations with males at as many as 6 different zones. Each zone, therefore, was a sort of hub at which males with different affiliations around the rim came into contact. Each of the 6 major perch-zones shared at least one constituent with each of the other zones. The mean number of males shared by zones was 3.9 ± 2.7 (range=1 to 9). Marked changes occurred in male traits with increasing age and status. These included (1) Significant declines in weight throughout the lifespan, (2) a 4-year delay in plumage maturation with well-defined stages, (3) reduction in the number of zones with which males maintained affiliations, and (4) increasing probability of copulatory success (restricted to a small subset of the oldest males, ≥ 10 years of age). Variance in copulatory success was the highest yet described for birds. Of 85 males monitored between 1983 and 1986, copulations (n=121) were distributed among only 8 males. Four of these males accounted for over 90% of the copulations, with 63% accruing to one male. The beta male of this alpha copulated twice in the absence of his partner; all the other copulaters were alphas. I examined correlates of male mating success. Female visitation correlated with the number of unison 'toledo' calls given. If a female visited, copulatory success correlated both with a residual effect of the 'toledo' output and with the duration of the 'butterfly' component of the dual-male dance performance. My correlational results suggest that females do choose, on the basis of performance cues, among the small subset of males that are well-established alpha and beta partners. Development of alliances, as much as male combat, may determine attainment of high-performance partner status. Thus, sequential male-male interactions and female choice appear to produce nested subsets of successful males leading to an extreme in variance in male mating success. Males unsuccessful in male-male interactions are not 'eligible' for female choice. By requiring partnered display, females may be implicitly narrowing the subset of potentially successful males. In other lek systems the union, rather than the intersection, of the subsets produced by intra- and intersexual selection may include successful males. In that case, intrasexual selection via disruption of copulations may enlarge the pool of potentially successful males under intersexual selection and produce lower variances in male mating success. Students of sexual selection may need to consider the extent to which intra- and intersexual selection interact as union or intersecting sets to produce variance in male mating success.

Sexual selection is usually invoked to explain the evolution of elaborate epigamic characters in animals. However, the mechanism by which female choice operates is poorly understood, and it is not clear whether female choice is purely aesthetic or related to male genotypic quality. It has been suggested that Moller's fluctuating asymmetry (FA) hypothesis may resolve the 'arbitrary trait'-'good gene' debate. However, tests of this controversial hypothesis have yielded equivocal results. I examined the allometric patterns of FA in the redcollared widow in order to test the FA hypothesis. In addition, I documented intrapopulation variation in trait size to determine whether females could distinguish between males on the basis of ornament size and/or symmetry. Male tail length was found to be more variable in size than other traits, suggesting that sufficient variation exists in ornament size for females to distinguish between males on this basis. In addition, the prediction of the FA hypothesis that ornaments would display higher degrees of asymmetry than non-ornamental traits was supported. However, no significant linear or second-order polynomial relationship was found between trait size and asymmetry for tail, wing and tarsus length. Furthermore, neither tail length or symmetry was correlated with indices of body condition. Although this might suggest that the FA hypothesis is invalid, I argue that the assumptions of the hypothesis are too simplistic for it to hold true for all species without taking the basic biology of the species into account. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 1997.

I studied the mating behaviour of Richardson’s ground squirrels (Urocitellus richardsonii) in 2007 and 2008, near Picture Butte, AB, Canada with the goals of evaluating multiple paternities within litters, sperm competition, and female mate choice. Eleven microsatellites and use of behavioural data to eliminate males who could not be putative sires based on their spatial and temporal remoteness from estrous females enabled exclusive assignment of paternity to 82.8% of 598 offspring with known maternity. The frequency of multiple paternities (26.4%, n=87 litters) in my population was lower than that reported for Richardson’s ground squirrels in a Manitoba population (80.0%, n=15 litters). Sperm competition was absent except in litters weaned by those females that mated again within 5 minutes of the first copulation, in which case sperm displacement was evident. Female choice was observed through avoidance of copulation, termination of copulation, and hide-then-run behaviour. / x, 98 leaves ;|c29 cm. --

Thesis (Ph. D.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 124-140). Also available on the World Wide Web.

Thesis (M.S.)--State University of New York at Binghamton, Department of Biological Sciences, 2009. / Includes bibliographical references ( leaves 46-48).

Thesis (M.Sc.)--Memorial University of Newfoundland, 2003. / Includes bibliographical references. Also available online.

Thesis (Ph. D.)--Oregon State University, 2011. / Printout. Includes bibliographical references (leaves 92-102). Also available on the World Wide Web.

Thesis (Ph. D.)--University of Missouri-Columbia, 2007. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on October 18, 2007) Vita. Includes bibliographical references.