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Spotted owls in harvested areas /Nickell, Kathleen R. January 1986 (has links) (PDF)
Thesis (M.S.)--Eastern Illinois University. / Includes bibliographical references (leaves 44-46).
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Winter movements and habitat use of northern saw-whet owls at Assateague Island, MarylandChurchill, John B. January 1900 (has links) (PDF)
Thesis (M.S.)--West Virginia University, 1998. / Title from document title page. "Nov. 11, 1998." Document formatted into pages; contains xi, 84 p. : ill. (some col.), maps (some col.) Includes abstract. Includes bibliographical references.
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Ecology and management of large forest owls in south-eastern AustraliaKavanagh, R. January 1997 (has links)
Thesis (Ph. D.)--University of Sydney, 1997. / Bibliography: leaves 382-422. Also available in print form.
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Habitat selection by Northern Pygmy-Owls on the Olympic Peninsula, WA /Giese, Alan R. January 1900 (has links)
Thesis (M.S.)--Oregon State University, 2000. / Typescript (photocopy). Includes bibliographical references (leaves 32-34). Also available on the World Wide Web.
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Diet and habitat of the powerful owl (Ninox strenua) living near MelbourneLavazanian, Elizabeth, elizabeth.lavazanian@deakin.edu.au January 1996 (has links)
The diet of Powerful Owls (Ninox strenua) living at Christmas Hills, 35km north-east of Melbourne was examined by analysis of 686 regurgitated pellets collected over two years.
An aid was also developed to help identify potential mammalian prey species based on hair and skeletal characteristics. The following features were found to be most useful in distinguishing between the three species of arboreal marsupials - Common Ringtail Possum (Pseudocheirus peregrinus), Common Brushtail Possum (Trichosurus vulpecula) and Sugar Glider (Petaurus breviceps):
- Cross-sectional width of primary guard hairs.
- The size and shape of the nasal, frontal, parietal and squamosal bones of the skull.
- Dentition. The size and shape of the upper incisor, canine and premolar teeth. The size and shape of the lower incisor and premolar teeth.
- The size of the humerus. The Sugar Glider has a much smaller humerus than that of the Common Ringtail Possum and the Common Brushtail Possum. In the Common Brushtail Possum the entepicondyle ends in a very sharp point but the Common Ringtail Possum this point is not as sharp.
- The Common Ringtail Possums femur has a very prominent trochanter which projects further than that in the Common Brushtail Possum. The femur of the Sugar Glider is distinguished by having a very large depression between the condyle and the trochanter.
- The Common Brushtail Possums scapula has a narrower lower blade (relative to length) than that in the Common Ringtail Possum. The scapula of the Sugar Glider is smaller in size than that of the other two possums.The pelvic girdle Of the Common Brushtail Possum has a much wider ischium than those of the Common Brushtail Possum and the Sugar Glider. The ilium of the Sugar is much narrower and smaller than that of the other two possums
Mammalian prey was found in 89%, insects in 13% and birds in 10% of the pellets. Of the mammals, Common Ringtail Possums occurred most frequently in the pellets over the year. There was no seasonal difference in the frequency of occurrence of Common Ringtail Possums and Sugar Gliders in pellets. However, Common Brushtail Possums were more likely to be taken in spring than in the other seasons. More adult Common Ringtail Possums were taken as prey than were other age classes over the year, except in summer when high numbers of young were consumed by the owls.
The habitat of the Powerful Owl was examined by ground surveys and spotlight surveys in sixteen sites within the Warrandyte-Kinglake Nature Conservation Link. Four categories of survey sites were chosen with the following features.
Category A - Sites with a dense understorey of shrubs and small trees, as well as many old trees (>10/ha) which might be suitable for nest hollows.
Category B - Sites which lacked a dense understorey of shrubs and small trees and containing few or no old trees suitable for nest hollows.
Category C - Sites with a dense understorey of shrubs and small trees but containing few or no old trees suitable for nest hollows.
Category D - Sites which lacked a dense understorey of shrubs and small trees but having old trees (>10/ha) which might be suitable for nest hollows.
High prey densities strongly correlated with the presence of hollows at these sites.
In the light of the results, management recommendations were made for the future conservation of the Powerful Owls living at Christmas Hills. The following recommendations were particularly important:
1. Cleared or semi - cleared land within the Warrandyte Kinglake Nature Conservation Link be revegetated using indigenous species of eucalypts and waffles in order to
provide a contiguous native forest corridor for the movement of possums and gliders between the Yarra River Valley and the Kinglake Plateau.
2. Continued planting of Eucalyptus spp. and Acacia spp. in the forested areas of the Warrandyte-Kinglake Nature Conservation Link.
3. Continued protection of healthy living trees to provide a continuous supply of hollow trees.
4. No falling of dead standing trees for firewood collecting as these can provide nest hollows for prey species of the Powerful Owl.
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The effects of release techniques on the reproductive performance and post-fledging juvenile survival of captive-bred Western Burrowing Owls (Athene cunicularia hypugaea) in the Nicola Valley, British ColumbiaMitchell, Aimee Marie 05 1900 (has links)
Reintroduction of captive-bred Western Burrowing Owls (Athene cunicularia hypugaea) in the Nicola Valley, British Columbia, has had limited success in increasing the local breeding population. Traditionally, yearling captive-hatched Burrowing Owls that were paired and released into artificial burrows in the field, held overnight, and provided with supplemental food throughout the breeding season (hard release) have had high post-release dispersal and mortality. In 2005 and 2006, I used an alternative soft-release technique to test for an improvement upon the hard-release technique. The soft release followed the same procedure as the traditional hard release but also included enclosures around burrow entrances to contain the owls for a 2-week period in the field prior to release. I compared immediate post-release dispersal, seasonal survival, and reproductive success for 37 hard-released and 30 soft-released pairs. I radio-tagged 39 of these released owls in order to accurately monitor their activities, regardless of whether they remained at release sites or dispersed. The soft-release technique led to 20% more owls remaining at the release sites, 14% more owls surviving the breeding season, and 20% more owl pairs fledging juveniles.
In addition to investigating adult survival and reproductive success, I examined post-fledging juvenile survival, local recruitment, and habitat use, and adult prey consumption behaviour in order to assess the potential of these aspects to limit the success of the reintroduction. Survival and local recruitment rates of the juveniles of captive-bred adults released with two different techniques were similar to that of juveniles of wild adults in the same study area or in other parts of the Burrowing Owl's range. Juvenile habitat-selection analyses identified the importance of rangeland, and comparisons of prey consumption revealed the rapid development of foraging abilities by captive-bred Burrowing Owls. I concluded that these aspects of the owl's ecology were not negatively affected by a captive upbringing, and therefore not likely limiting the success of the reintroduction.
Overall, the use of an enclosure-based soft-release technique addresses major limitations to the success of releases, and shows promise for increasing the breeding population in this region. This approach can also be applied to recovery efforts throughout the Burrowing Owls' range, and provide guidelines for other species' reintroduction programs.
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Raptor assemblage, abundance, nesting ecology, and habitat characteristics under intensive forest management in the central Appalachian MountainsSmith, Rebecca D. M., January 2003 (has links)
Thesis (M.S.)--West Virginia University, 2003. / Title from document title page. Document formatted into pages; contains xii, 106 p. : col. ill., col. maps. Includes abstract. Includes bibliographical references.
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Aerodynamic measurements on some special wing features of nocturnal owls and their acoustic significanceGerakis, J.G. (Jeffrey George) January 1985 (has links)
No description available.
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A taxonomic study of the Haemoproteidae (Apicomplexa : Haemosporina) of the Avian order Strigiformes /Bishop, Madonna Anne Whiteway. January 1989 (has links)
Thesis (M.Sc.) -- Memorial University of Newfoundland, 1989. / Typescript. Bibliography: leaves 53-57. Also available online.
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DERIVED RELATIONAL RESPONDING: ASSESSING THE RELATIONSHIP BETWEEN THE PEAK-E AND OWLS-II ASSESSMENTSRieder, Kerry Ann 01 August 2016 (has links)
The current study examined the relationship between the relational abilities of 13 children (92.31% of which were diagnosed with autism) and their corresponding performance on a widely used language assessment tool. The relational abilities of the participants were assessed using the Prompting the Emergence of Advanced Knowledge Equivalence Pre-Assessment (PEAK-E) and language skills were assessed with the Oral and Written Language Scales- Second Edition (OWLS-II). The data indicated a strong, significant correlation between participant scores on the PEAK-E and the OWLS-II assessments (r = .888, p<.01) which is further analyzed in each of the four subsets of the OWLS-II Oral Expression (r = .861, p<.01), Listening Comprehension (r = .84, p<.01), Written Expression (r = .792, p<.01), and finally Reading Comprehension (r = .762, p<.01). Results further demonstrate the validity of the PEAK-E assessment in individuals with autism and other related disorders.
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