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Predation is an important ecological process that shapes life-history traits, community dynamics, and species coexistence and therefore has been suggested to explain many patterns in avian ecology. Although many studies have reported spatial, temporal, or interspecific patterns in nest predation, relatively few studies have been designed to identify the specific mechanism(s) that underlie these patterns. I examined mechanisms underlying the risk of nest predation in birds by (1) reviewing nine of the most commonly cited hypotheses to explain spatial, temporal, and interspecific variation in the risk of nest predation, (2) conducting a comparative analysis of the nest-concealment hypothesis to examine which methodological issues, extrinsic factors, and species traits influence whether or not foliage density affects the risk of nest predation, and (3) testing six mechanistic hypotheses to determine the underlying cause(s) of intra-seasonal decreases in the risk of nest predation.Many of the hypotheses invoked to explain spatial, temporal, and interspecific variation in the risk of nest predation lack clearly defined mechanisms. I suggest that future studies explicitly define the mechanism and assumption(s) of each hypothesis prior to implementing empirical tests.I found that the discrepancy in results among past studies that have examined the nest-concealment hypothesis was due to interspecific differences in a variety of intrinsic and extrinsic factors that affect nest predation but have previously been ignored. The effects of nest concealment on nest placement and probability of nest predation vary among species and this variation is predictable based on the bird's morphological traits and characteristics of the ecosystem.Increased risk of nest predation early in the breeding season appears to be due, in part, to foliage phenology and spatial and temporal changes in predator behavior. The risk of nest predation was negatively associated with foliage density early, but not late, in the breeding season. Supplemental food provided to nest predators resulted in a numerical response by nest predators, increasing the risk of nest predation at nests located near feeders. I show that intra-seasonal changes in environmental features and predator behavior affect patterns of nest predation, which can influence timing of breeding.

A functional understanding of how phenotypic traits may affect growth, reproduction and survival is necessary to understand their ecological and evolutionary consequences. Larval dragonflies (Odonata: Anisoptera) swim using jet propulsion, likely controlled by abdominal traits and perhaps to escape fish predators. I investigated whether abdominal morphology explains swimming performance and if either explains the distribution of larvae among ponds that vary in predation risk. I recorded and measured the swimming performance of dragonflies responding to simulated attack and tested relationships with abdominal traits expected to influence jet thrust force generation. Variation in swimming performance was explained by abdomen dry weight, ventral surface area, and abdominal segment 10 width across genera as hypothesized. High-performance dragonflies were more likely to occur in ponds containing predatory fish. This is the first investigation of the morphology responsible for jet propulsion, and the relationship between swimming performance and larval dragonfly ecology.

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Data taken from the literature were used to develop and evaluate models predicting fish biomass and yield, crustacean zooplankton biomass, and profundal macrobenthos biomass in lakes. Total phosphorus concentration and macrobenthos biomass/mean depth were the best univariate predictors of fish biomass and yield. Phosphorus concentration was also the best predictor of zooplankton and macrobenthos biomass. In experiments testing for inter- and intraspecific competition, conducted in situ at densities based on measured natural fish densities, growth of yellow perch (Perca flavescens) and pumpkinseed (Lepomis gibbosus) reared alone was inversely related to density. Both species primarily ate macroinvertebrates when reared alone. When reared together: perch growth was significantly depressed compared to that of perch reared alone; pumpkinseed growth was equivalent to that of pumpkinseed reared alone; and the diet of perch changed to include food of inferior quality (microcrustaceans) in the presence of the superior competitor, pumpkinseed, whose diet did not change.

It is only recently that studies have explored the use of olfaction in birds. Birds are now known to use odour cues for navigation, and locating food. Odours produced by the birds themselves can also function in nest recognition and even mate choice. The odours of most birds stem from the preen wax produced by the uropygial or preen gland. The wax is comprised of a complex mixture of esters and volatiles, and is known to vary in some species with age, sex, season, or environmental conditions. Its function has been associated with feather maintenance, but it may also play a role in sexual selection and chemical communication. In this thesis, I used the preen gland and its preen wax to perform comparative studies on the evolution of odours between island birds and their continental relatives. I used the birds of the Oceania region as a model system, where most passerines originated from continental Australia but have colonised numerous surrounding islands such as New Zealand and New Caledonia. As islands generally lack mammalian predators, and have less parasites and less interspecific competition than continents, these differences in environmental conditions likely shaped functional differences in the preen gland and its products. I measured the size of the preen gland and collected preen wax from a variety of forest passerines in Australia, New Zealand and New Caledonia. I found that island birds have larger preen glands and therefore likely produce more preen wax than their continental relatives. I also found that the preen wax composition differed among species, with a shift to birds on islands producing disproportionately lighter and more volatile compounds. I suggest that selection favoured the gain of more volatile molecules in island birds as they were released from the constraint to camouflage their odours that is imposed by mammalian predators on continental areas. It is possible that this also allowed greater communication through olfactory channels in island birds, and such communication is enhanced through the use of more volatile compounds. To support this hypothesis I showed that the South Island robin (Petroica australis) was able to detect and react to the odour of a conspecific (odours produced by preen wax) in the absence of any visual cues. From a conservation perspective, increased volatility of the preen waxes of island birds might place them at increased risk from introduced mammalian predators that use olfaction to locate their prey. However, in both laboratory tests using Norway rats (Rattus norvegicus), a common exotic predator, and in field trials using rodent tracking tunnels, I found only limited evidence to suggest the odour of island birds places them at greater risk, and more experiments are needed to test this hypothesis. Finally, my findings of more conspicuous odours in island birds suggest new avenues of research for their conservation, including whether island species that seem especially prone to predation have preen waxes (and thus odours) that are also especially attractive to exotic mammalian predators. Conservation programmes to protect endangered island birds may even benefit from considering whether olfactory cues can be minimised as a method of reducing predation risk.

Seed dispersal in New Zealand relies on a different guild from the one present before the arrival of humans into the islands. Post-dispersal biotic and abiotic filters have also changed due to the introduction of seed predators and herbivores. The aim of this thesis was to evaluate the actual contribution of seed dispersers to the patterns of seed fall and to understand the effects of biotic (seed density, predators, distance from conspecifics) and abiotic (pH, canopy openess, etc) factors on seed and seedling survival. I expected that tree species with different fruit sizes would be selected by different assemblages of dispersers, therefore being deposited and recruiting differentially on the forest floor. I analyzed the changes in small-scale seed diversity with the use of seed traps during two seasons in two 0.36 ha plots in a mixed broadleaf-podocarp temperate forest. The diversity of seeds was lower for in-fruit seeds (1.40 species per grid-cell) than for bird-dispersed seeds (2.62). The dominant species D. cupressinum was dispersed towards con- and heterospecific canopies (wind-dispersed trees Weinmannia racemosa and Metrosideros umbellata), giving a probable mechanism for the observed increase in finescale seed diversity. Then, using a 12-year dataset on seed fall I analyzed the changes in ground-level seed heterogeneity generated by bird-dispersed seed rain (propagule-scale) relative to the canopy composition (adult-scale) on six tree species. A Non Metric Multidimensional Scaling analysis demonstrated that the differences in species composition between sampling points (seed traps) were larger for tree canopies than for dispersed seeds. Different tree species acted as seed importers and/or exporters, although these patterns were not explained by fruit size or the richness of the disperser assemblages. I also investigated the effects of seed and seedling density on seed predation, seedling emergence and seedling survival to 12 months of five tree species. Seed predation increased with seed size, and it was higher at high density only for the largest-seeded species Beilschmiedia tawa and Prumnopitys ferruginea. Access of seed and seedling predators to the propagules was the main factor affecting seedling emergence and seedling survival. Abiotic variables were important for germination and seedling survival of the two small-seeded species, but only biotic predictors (mammalian exclosure and density) were important for medium and large-seeded species. Finally, using a split-plot experimental design I measured the effects of (a) the presence of conspecific canopy, (b) high conspecific seed densities and (c) introduced (or invasive) mammal access on seedling emergence and seedling survival (Janzen-Connell effects). Distance effects were stronger than density effects, and mediated by native and exotic predators. Final survival under conspecifics was strongly reduced in both species, with zero survival of B. tawa under conspecifics, and near zero (2/896) under D. dacrydioides. Seed dispersal service in New Zealand is still enough to produce changes in the spatial pattern of seed deposition in the forest. Post-dispersal processes such as seed predation and herbivore are having strong impacts on the survival and potential recruitment of plant species. Large-seeded trees are the most affected in terms of the impact of introduced mammals on seed predation, but seedling survival is affected independent of seed size. However, it is unknown how different these ecological processes are from the original situation without pests in New Zealand. The results of my research can contribute with valuable information for future research trying to understand the consequences of seed dispersal for recruitment, as well as inform complex models that try to predict the long-term impacts of the exotic mammals introduced in New Zealand.

The fossil record of drilling predation has been widely used to study predator-prey interactions and their relative importance on long-term evolutionary processes. Incomplete drill holes have been interpreted as indicators of failed attacks due to well-defended prey. However, this interpretation is based on pair-wise interactions between one predator and one prey, a condition commonly compromised in nature. The hypothesis that interference among drilling predators leads to an increase in the relative frequency of incomplete drill holes was tested in the laboratory using the naticid Neverita delessertiana (R cluz) and a common prey, the bivalve Chione elevata (Say). The experiment consisted of an isolation treatment, where predators fed alone, and a competition treatment, where predators fed in groups of three. Predators in competition were grouped into two size cohorts, small and large. All drilling attacks made by isolated predators of both size groups were successful, resulting in complete drill holes, whereas, in competition, the incomplete drilling frequencies were 6.9% for the small predator group and 21.3% for the large predator group. A range of competitive, predator-predator interactions were observed, including grappling, prey theft, and cannibalism. These results suggest that interpretations of both field and fossil data must consider the role of competitive disruption as an additional source of incomplete drill holes. The implications of other observations, including prey 'suffocation' and the resumption of incomplete drill holes after successful prey theft, are also discussed.