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North American grassland bird populations are declining more rapidly than other groups of birds. A well-established method of quantifying and monitoring grassland bird populations is by locating active nests. Active nests are often difficult to locate in grassland swards due to the varying heights within the canopy that nests are established. Studies quantifying grassland bird populations have low statistical power due to low sample sizes and high disturbance. Advances in small, unmanned aerial systems and thermographic imaging technologies have potential to improve efficiency of locating nests throughout canopies. This study explored detection accuracy of using thermal imagery to identify simulated grassland bird nests located at different heights within monoculture tall-stature grass canopies. This methodology was tested in blind evaluations, using multiple evaluators. Results from this study suggest that surveying thermal images is a reliable method for detecting active nests at depths of up to 1 m into a grass canopy.

Three tern species, Roseate Tern (Sterna dougalli), Bridled Tern (Sterna anaethetus) and Crested Tern (Sterna bergii) co-bred at Baisha islet, east-north of Penghu, in the summer of 2006. Each species favored different kind of environment for nesting. All Crested Terns nested in the flat plane with vegetation; Roseate Terns in the cliff near the vegetation, and Bridled Tern primarily nested near the vertical rock or under a rocky roof. The Crested Tern had the highest nesting density, and Bridled Tern nested loosely. The hatching success of Roseate (75%) and Crested Tern (73%) were significantly higher than that of Bridled Tern (30%). Roseate and Crested Tern laid eggs synchronously and had apparently two wave of egg laying and the breeding performances between early- and late-laying period were quite different. The relationship between hatching success and nest-site characteristics of the three species was investigated. The results revealed that hatching success of Roseate Tern increased with the number of walls and neighbors. Early-laying nests (79%) and central nests (72%) were more successful than late (11%) and edge nests (45%) of Roseate Terns. The laying-period was also important factors affecting hatching success of Crested Tern. Overall, the low hatching success of the late-laying nests may be due to the change of environmental conditions and the losing advantage of group breeding in the late season. The low hatching success of Bridled Tern was considered owing to the asynchronous laying pattern, loosely built nesting and weak parental behaviors.

Habitat selection theory presumes that organisms are not distributed randomly in their environments because of habitat-specific differences in reproductive success and survival; unfortunately, many previous studies were either unable or failed to look for evidence of processes shaping nest site selection patterns. Furthermore, little is known about adaptive nest site selection in northern environments where habitats often have little vegetation and time and climatic constraints may be pronounced. Therefore, I investigated patterns of nest site selection by common eider ducks (<i>Somateria mollissima</i>) at an island colony in Canadas Eastern Arctic, and looked for evidence of selective processes underlying these patterns by employing experimental and observational techniques.<p>I characterized physical features of (a) non-nest sites (b) active nest sites and (c) unoccupied nest sites that had been used in previous years. Habitat features that distinguished non-nest sites from unoccupied nest sites were also important in distinguishing between active and unoccupied nest sites during the breeding season. Active nest sites were closer to herring gull (<i>Larus argentatus</i>) nests, farther from the ocean and had organic substrates. In general, habitat features associated with nest use were not strongly associated with success after the onset of incubation. Nests near fresh water ponds were more successful in one study year, but in the other two study years successful nests were initiated earlier and more synchronously than were unsuccessful nests. Common eiders settled to nest first near the geographic centre of the colony, whereas sites near the largest fresh water pond were occupied later; distance to ocean had no observable effect on timing of nesting. Nest density was greater farther from the ocean, but timing of nest establishment did not differ between high and low density plots. <p>I tested whether moss or duck down placed in nest bowls could increase nest establishment, or advance laying date. I placed this extraneous material in bowls before nesting and found no difference in likelihood of nest establishment; however, bowls containing duck down were initiated earlier (or had higher survival) than those containing no nesting material. To investigate the role of nest shelter and microclimate in nest site choices and female body condition, I placed plywood nest shelters over established nests. Temperature probes indicated that artificially-sheltered females experienced more moderate thermal environments and maintained higher body weight during late incubation than did unsheltered females. However, few eiders nested at naturally-sheltered sites, possibly because nest concealment increases susceptibility to mammalian predators. My results suggest that eider nest choices likely reflect trade-offs among selective pressures that involve the local predator community, egg concealment, nest microclimate and energy use.

Habitat selection theory presumes that organisms are not distributed randomly in their environments because of habitat-specific differences in reproductive success and survival; unfortunately, many previous studies were either unable or failed to look for evidence of processes shaping nest site selection patterns. Furthermore, little is known about adaptive nest site selection in northern environments where habitats often have little vegetation and time and climatic constraints may be pronounced. Therefore, I investigated patterns of nest site selection by common eider ducks (<i>Somateria mollissima</i>) at an island colony in Canadas Eastern Arctic, and looked for evidence of selective processes underlying these patterns by employing experimental and observational techniques.<p>I characterized physical features of (a) non-nest sites (b) active nest sites and (c) unoccupied nest sites that had been used in previous years. Habitat features that distinguished non-nest sites from unoccupied nest sites were also important in distinguishing between active and unoccupied nest sites during the breeding season. Active nest sites were closer to herring gull (<i>Larus argentatus</i>) nests, farther from the ocean and had organic substrates. In general, habitat features associated with nest use were not strongly associated with success after the onset of incubation. Nests near fresh water ponds were more successful in one study year, but in the other two study years successful nests were initiated earlier and more synchronously than were unsuccessful nests. Common eiders settled to nest first near the geographic centre of the colony, whereas sites near the largest fresh water pond were occupied later; distance to ocean had no observable effect on timing of nesting. Nest density was greater farther from the ocean, but timing of nest establishment did not differ between high and low density plots. <p>I tested whether moss or duck down placed in nest bowls could increase nest establishment, or advance laying date. I placed this extraneous material in bowls before nesting and found no difference in likelihood of nest establishment; however, bowls containing duck down were initiated earlier (or had higher survival) than those containing no nesting material. To investigate the role of nest shelter and microclimate in nest site choices and female body condition, I placed plywood nest shelters over established nests. Temperature probes indicated that artificially-sheltered females experienced more moderate thermal environments and maintained higher body weight during late incubation than did unsheltered females. However, few eiders nested at naturally-sheltered sites, possibly because nest concealment increases susceptibility to mammalian predators. My results suggest that eider nest choices likely reflect trade-offs among selective pressures that involve the local predator community, egg concealment, nest microclimate and energy use.

Predators are a threat to many ground-nesting shorebirds, although it remains largely unknown how they interact with passive predator management techniques such as nest exclosures. I examined the effects of nest exclosures on incubating Piping Plovers (Charadrius melodus melodus) and their predators on nesting beaches in Kouchibouguac and PEI National Parks. A combination of behavioural observations, video monitoring of nests and an artificial nest experiment was used to examine the effects of nest exclosures in this study system. The behaviour of Piping Plovers did not differ between exclosed and unexclosed nests, although different types of predators seemed to have an effect on plover nest attentiveness. Predators visited exclosed nests more often than unexclosed nests and spent more time in the vicinity of exclosed nests than unexclosed nests. Since increased adult mortality and nest abandonment have been documented at exclosed Piping Plover nests, as well as nests of other shorebirds, the results of this study provide evidence of a link between predator harassment and these negative effects.

Many factors affect the productivity of songbirds. Which vegetation types the birds inhabit, nest-site characteristics, and adult behavior at the nest may affect predation and parasitism frequencies, fecundity, and nest survival and fledgling survival. All of these metrics determine reproductive success of individuals and may influence population persistence, especially for threatened and endangered species. My research investigated factors that affected these metrics for endangered black-capped vireos (Vireo atricapilla). Shrubland is considered high quality vireo habitat, with woodland vegetation types considered marginal. I located and monitored nests, conducted nest behavior observations, recorded behavior and predation at nests using video cameras, and resighted fledglings in shrubland, oak-juniper woodland, and deciduous woodland during the 2008–2010 breeding seasons. I monitored 302 black-capped vireo nests in 259 territories and resighted 350 fledglings with unique color combinations. Apparent nest success, nest survival, success of first nest attempts, parasitism and predation frequency, and fecundity did not differ statistically among vegetation types. Parasitism frequency was nearly twice as high in shrubland (22 percent) than in either woodland (12 percent in each) and varied by year. Nest-site characteristics differed among vegetation types, but nest survival was affected only by nest height and year; nests placed higher from the ground and nest attempts in 2008 and 2009 had lower survival. Fledgling survival was not affected by vegetation type or proximity of the nest to oak-juniper woodland. Nest behavior was not affected by vegetation characteristics, though nest attentiveness during incubation increased as average cover from 0 to 2 m increased. Females spent 80 percent more time on nests during incubation and 250 percent more time on nests during the nestling stage than males, but visitation was similar for each sex. Overall, the probability of nest success improved as male participation increased. My results emphasize the importance of male participation in determining the outcome of nests for species exhibiting bi-parental care. Furthermore, woodland habitats previously considered marginal may be good quality habitat in areas with large populations of black-capped vireos. Recognizing woodlands as non-typical, yet still suitable, habitat will allow managers to incorporate these vegetation types into management plans and recommendations for landowner conservation incentive programs.

This study is dealing with questions of environmental influences on predation risk in Northern Lapwings nests. I for example measured and evaluated nest krypsis and counting nest densities. I as well did marking of nests and dealed with question whether it has influence on nest predation. Another part of this resech was identifying of Lapwings nests predator.