Thesis (Ph. D.)--University of Florida, 1984. / Description based on print version record. Typescript. Vita. Includes bibliographical references (leaves 211-224).

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Across avian systems, plumage ornamentation is often considered a signal of individual fitness, condition, sex, or status, and varies due to genetics or environmental sources. In species with structural coloration, plumage variation results from differences in the amount of energy allocated to feather growth during molt, presenting a unique opportunity to study the link between individual quality and ornamentation. In cooperative breeding species, such as the Florida Scrub-Jay (Aphelocoma coerulescens), the role of structural color as a signal is particularly important because helpers may delay breeding for one to several years and competition for space is high. Florida Scrub-Jay juveniles are sexually dimorphic in the ultraviolet range, and plumage color predicts social dominance and condition, but not adult reproductive fitness. Little is known about the consistency of ultraviolet reflectance across molts, and I tested the following questions: 1) does plumage color change across molts within individuals; 2) how do environmental variables and stress affect structural color; and 3) does adult color or change in color predict reproductive fitness? I measured relative change in color within individuals by comparing their juvenile and first set of adult feathers after pre-basic molt. I used several measures of nutritional condition, social dynamics, habitat quality, and parasite infection to model color, and I experimentally administered corticosterone during pre-basic molt to examine the effects of increased stress on color. Plumage reflectance was compared with breeding status to investigate the role of color in breeding space acquisition. Plumage reflectance was significantly different within individuals across molts, but juvenile and adult color were correlated. Adults were significantly less bright than juveniles, with higher proportions of UV chroma and hues shifted toward UV wavelengths. Variation in feather color was best explained by sex, mass, parasite infection, and an interaction between area of oak scrub and group size. Juvenile feather color was also strongly associated with mother ID, but this was not the case for adults even though adult color was correlated with juvenile color. Adult chroma was reduced in birds treated with corticosterone, and hues were shifted toward longer wavelengths. No measure of adult color predicted acquisition of breeding space, but change in brightness and hue were significant predictors of acquisition for females, where breeders tended to experience greater reductions in brightness and shifts toward UV hues compared to helpers. This may be due to sex-specific differences in reproductive strategies in Florida Scrub-Jays. Females tend to disperse farther distances and breed earlier than males, potentially expending more energy foraying and searching for breeding space, which could reduce brightness if it is linked with condition. These results suggest that sexual selection is not a dominant factor in plumage ornamentation for Florida Scrub-Jays, and understanding the interaction between plumage color, personality, and reproductive fitness should be a priority for future research.

This report evaluates vocal communication, nesting, territoriality, and other social behaviors of the California Scrub Jay.

Individual organisms often use cues from their natural environments to determine many behavioral and life-history "decisions." These "decisions" are usually adaptive, i.e. a response to selection, because the environmental cues on which they are based reliably correlate with increased fitness over time. When the selected behavioral response to a natural cue no longer provides a fitness benefit, then selection for a new response may occur but individuals maintaining the previously selected response may suffer reduced survival and reproduction. Especially in human-modified landscapes individuals making a maladaptive behavioral or life-history choice based on those formerly reliable environmental cues may be faced with an "evolutionary trap". In urban, or suburban, environments many factors have been altered in ways that could lead to evolutionary traps. Inappropriate behavioral responses by many individuals could lead to reduced demographic performance of urban populations relative to their wildland counterparts and to the decline of entire urban populations. In birds, maladaptive patterns of nest provisioning or vigilance may occur (a) when human-provided adult foods are easier to feed young because they are more abundant and predictable than foods appropriate for nestlings, or (b) when birds' perception of predation risk, which can be influenced by human disturbance, is greater than the real risk. By provisioning or attending their nests more or less than what is appropriate given the environmental level of resources and risks, the behavior of suburban parents may be contributing to high levels of nest failure during the nesting stage. To determine whether maladaptive parental care influences nest survival during the nestling stage, I conducted an experiment using Florida Scrub-Jays (Aphelocoma coerluscens). Suburban scrub-jays have lower nest survival during the nestling stage but higher survival during the incubation stage relative to wildland jays. Both predators and food abundance vary greatly between suburban and wildland scrub. The suburbs have a greater abundance of predators that may prey on both adult scrub-jays and their nests and more foods appropriate for adults but less nestling-appropriate food. This variation in risks and resources should affect the parental care behavior of suburban scrub-jays, which in turn may affect patterns of nest survival. In pre-treatment observations, I found that suburban females spent more time brooding than wildland birds but suburban males did not provision any more than wildland males. Experimentally increasing the perception of adult predation risk reduced parental care in both suburban and wildland females. Increasing the availability of nestling food reduced parental care in suburban females but had no effect in wildland females. Increasing food availability, but not predation risk, decreased call rates but increased call frequency in nestling scrub-jays from both habitats. However, neither parental care nor food availability had much influence on nest survival during the nestling stage. Instead, side nest concealment and the presence of helpers were the most important variables in nest survival analyses prompting other explanations besides maladaptive parental behavior or lack of nestling food resources for the habitat-specific difference in nest survival during the nestling stage.

Ornamental traits are considered honest advertisements of fitness, and their evolution is usually explained in terms of sexual selection. This explanation remains unsatisfactory in some instances, for example, juvenile birds whose plumage is molted prior to adulthood and breeding. I first evaluate whether juvenile plumage reflectance signals dominance status in the Federally Threatened Florida scrub-jay (Aphelocoma coerulescens) using a combination of observational and experimental methods. Then I estimate the heritability, non-genetic maternal and environmental effects, and strength of selection on juvenile plumage reflectance using archived feather samples and a pedigree constructed from historical nest records. Finally, I compare plumage reflectance and its use as a signal between a wildland and suburban population of scrubjays. I conclude that plumage reflectance is a signal of dominance, and that social selection can also drive the evolution of sexually dimorphic traits. In this species, plumage reflectance is heritable and influenced by maternal effects, but environmental effects are inconsequential. Although this trait appears to have an important function, only mean brightness and female hue are associated with lifetime reproductive success. Plumage reflectance was more UV-shifted in the suburban birds, but there is no reason to believe that urbanization decreases the value of this plumage as a signal. However, these plumage differences may facilitate dispersal from suburban areas, contributing to the decline of suburban populations.

For many organisms, embryonic development begins directly after an egg (ovum) has been fertilized by sperm; however, some organisms delay the onset of embryonic development until conditions are favorable for raising young. This delayed onset of development could occur by delaying implantation of fertilized ovum on the uterine wall, as seen in many mammals. Birds delay embryonic development by laying a set of fertilized ova over a period of consecutive days. These fertilized ova are protected from the ambient environment by an exterior shell, and it is in this shell outside of the female s body that embryonic development occurs, but only when females initiate incubation. The number of fertilized ova (eggs) that can be laid by a single female in a single clutch varies among and within bird species, and understanding this variation remains a vital, unanswered question in ornithology. A latitudinal gradient in clutch size is widely recognized, but the reason for this pattern is unclear. Some birds lay relatively large clutches over many days, thus we should expect that eggs could withstand fairly long exposure to ambient temperature and remain viable. However, recent evidence suggests that egg viability declines with increased exposure to ambient temperatures. The egg viability hypothesis predicts that eggs will fail to hatch if exposed to warm ambient temperatures for prolonged periods. I conducted a natural experiment to determine whether egg viability can explain site-specific variation in hatching failure. Hatching failure is higher in a suburban population of Florida Scrub-Jays than it is in a wildland population, possibly because suburban scrub-jays lay larger clutches. Scrub-jays, like many bird species, lay one egg per day and begin incubation with the last-laid egg, thus first-laid eggs in the larger suburban clutches should be exposed to the warm ambient temperatures of sub-tropical Florida longer than first-laid eggs in the smaller clutches typical of the wildland population. As predicted, I found hatching failure is higher in first-laid eggs in the suburbs, and these eggs experience increased exposure to warm ambient temperatures. At both sites, females appear to begin incubation earlier in the laying period as ambient temperatures increase seasonally, possibly to minimize exposure to warm ambient temperatures and minimize hatching failure in first-laid eggs. However, early onset of incubation causes eggs to hatch asynchronously ( > 24 hours between the first and last-hatched egg), and hatching asynchrony increases within-brood size-asymmetries, which leads to an increased frequency of brood reduction (the nonrandom loss of last-hatched young because of starvation). Thus, a tradeoff may exist between beginning incubation earlier in the laying period to minimize hatching failure in first-laid eggs and delaying the onset of incubation to minimize hatching asynchrony and brood reduction. This tradeoff can have profound effects on avian clutch sizes, and may potentially explain the widely known negative relationship between latitude and clutch size.