Agricultural grasslands have replaced native Midwestern prairies in the form of pasture, idle cropland and conservation fields. The condition of these cover types directly and indirectly influences the distribution, variety and productivity of avian populations within these landscapes. CP33 habitat buffers are an incentive-based conservation practice specifically designed to increase upland bird habitat and productivity. Landowners are encouraged to remove row crops from production and return them to early successional grassland habitat along the margin of agricultural fields. However, buffers exhibit a high perimeter-to-area ratio, which may increase negative edge effects, thereby creating sink populations. During the 2013 and 2014 breeding seasons, I assessed grassland bird response to CP33 habitat buffers in southern Illinois. Focal species included the northern bobwhite (Colinus virginianus), dickcissel (Spiza americana), eastern meadowlark (Sturnella magna), field sparrow (Spizella pusilla), indigo bunting (Passerina cyanea), and red-winged blackbird (Agelaius phoeniceus). I used a hierarchical multiscale framework to examine the influence of habitat variables at multiple scales on avian abundance, species richness, and occupancy. I also used this same framework, and logistic exposure modeling, to examine daily survival rates of nests found within CP33 habitat buffers. Multiscale occupancy and logistic exposure models consistently performed better than single-scale models for focal bird species; however, relative importance of local variables and landscape variables differed considerably among focal species. Nest survival rate was not strongly affected by edge effects or edge type. Microhabitat variables were much more influential in predicting nest survival. In my study area, CP33 habitat buffers are unlikely to support source populations for most of the focal grassland bird species I studied. To increase nest survival rates within established CP33 habitat buffers, managers should focus on microhabitat vegetation characteristics. To increase bird occupancy of CP33 habitat buffers in southern Illinois, managers should increase the size of CP33 habitat buffers within a landscape having adequate grassland cover. However, managers should not consider CP33 habitat buffers a panacea for most grassland avian species.

Human beings of all cultures build some form of shelter, and the global distribution of Homo sapiens depends on this basic trait. All great apes (chimpanzee, bonobo, gorilla, and orangutan) build analogous structures (called nests or beds) at least once a day throughout their adult lives, which suggests that this elementary technology was present before the hominid lines separated. This thesis investigates the variability and function of specifically wild chimpanzee shelters. I compared characteristics of chimpanzee nests, nesting trees, nest shape, and architecture in two savanna-dwelling populations on opposite sides of Africa: Fongoli, Senegal, and Issa, Tanzania. Savanna habitats are the most extreme habitats in which chimpanzees survive today, and may represent a similar environment to that in which early hominins evolved in the Plio-Pleistocene (Chapter 2). Investigating variation in nest-building within and between these two extreme habitats made it possible to tackle hypotheses of the shelter function of nests (Chapter 3).The influence of environment, specifically the role of protection from disease vectors and fluctuating temperatures, was assessed through a novel experiment in which I slept overnight in arboreal chimpanzee nests and on the bare earth (Chapter 4). To assess whether or not nests serve as an anti-predation function, I compared nesting in Issa, where predators are abundant, to Fongoli, where they are absent (Chapter 5). I provided further support for the thermoregulatory function of nests by showing that chimpanzees build more insulating nests in adverse weather conditions (Chapter 6).Nest-building is a learned behaviour, but its ontogeny is little known. I investigated social sources of variation in nest building in Fongoli to examine whether sex and age differences exist in nest building duration, nest position, shape and architecture (Chapter 7). Finally, ecosystem engineering is a consequence of animal construction, from ants to humans. I investigated use-wear traces around nests to assess niche construction of nest- building. I showed that chimpanzees repeatedly re-used these specific nest-spots within trees, which are pre-fabricated for future building through repeated pruning and shaping of these structures (Chapter 8).Nest building in great apes may be the foundation of constructivity in hominids. This thesis describes proximate functions and influences on nest-building variation in wild chimpanzees that help to model the evolution of shelter in hominids.

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.

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No description available.

No description available.

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.