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Results for “Journal of Raptor Research”

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149 records · Page 9Linked to original sources
USGS1994

Survival and causes of mortality in juvenile Puerto Rican parrots

Fifteen juvenile Puerto Rican Parrots (Amazona vittata) from wild nests in 1985, 1986 and 1987 were radio monitored an average of 110 +- 15.9 (SE) d (range 4-209 d) post-fledgling. Minimum survival was 67% (n = 3) in 1985, 100% (n = 4) in 1986 and 43% (n = 7) in 1987. Most mortality (three of five deaths) occurred during the first 35 d following fledgling. A major cause of mortality was predation by raptors. This research shows that additional studies are needed to define mortality causes to juvenile and adult free-flying Puerto Rican Parrots and to develop management guidelines to increase survival.

Journal of Field Ornithology↗
USGS1987

Case histories of bald eagles and other raptors killed by organophosphorus insecticides topically applied to livestock

Since 1982 when secondary poisoning of a red-tailed hawk ( Buteo jamaicensis ) was documented following the recommended use of famphur applied topically to cattle, the Patuxent Wildlife Research Center has tested dead birds of prey for poisoning by famphur and other pouron organophosphorus (OP) insecticides. Brain cholinesterase (ChE) activity was first determined, then if ChE was depressed ≥50%, stomach and/or crop contents were evaluated for anti-ChE compounds. This report presents the circumstances surrounding the OP-caused deaths of eight bald eagles ( Haliaeetus leucocephalus ), two red-tailed hawks, and one great horned owl ( Bubo virginianus ) between March 1984 and March 1985. OP poisoning of raptors by pour-on insecticides in the United States is widespread, but its magnitude is unknown.

Journal of Wildlife Diseases↗
USGS1981

Species differences in hematological values of captive cranes, geese, raptors, and quail

Hematological and serum chemical constituents of blood were determined for 12 species, including 7 endangered species, of cranes, geese, raptors, and quail in captivity at the Patuxent Wildlife Research Center. Means, standard deviations, analysis of variance by species and sex, and a series of multiple comparisons of means were derived for each parameter investigated. Differences among some species means were observed in all blood parameters except gamma-glutamyl transpeptidase. Although sampled during the reproductively quiescent period, an influence of sex was noted in red blood cell count, hemoglobin, albumin, glucose, cholesterol, serum glutamic oxaloacetic transaminase, Ca, and P. Our data and values reported in literature indicate that most hematological parameters vary among species and, in some cases, according to methods used to determine them. Therefore, baseline data for captive and wild birds should be established by using standard methods, and should be made available to aid others for use in assessing physiological and pathological conditions of these species.

Journal of Wildlife Management↗
USGS2014

Northern bobwhite predator avoidance behavior in response to varying types of threat

The flight behavior and cover use of northern bobwhite (Colinus virginianus) have been examined in several studies, but the current data lack quantitative measures of how bobwhites respond to natural threats. We examined aspects of bobwhite behavior in response to 4 threat categories: researcher, hunter, raptor, and mammal. We found that bobwhite flight distance is best predicted by threat type and covey size, and bobwhite flight speed is best predicted by threat type. Bobwhites flushed by the hunter threat and the raptor threat selected for significantly taller obstruction at landing sites than was randomly available, with average heights of 6.2cm taller (P=0.034), and 38.1cm taller (P<0.001), respectively. Raptor-flushed bobwhites also selected for significantly denser shrub cover (42.2%, P<0.001) and a lower angle of obstruction (70.4 degrees, P<0.001) at landing points than was randomly available. In the process of data collection, we also observed bobwhite roost locations have lower visual height obstruction (7.3cm, P=0.03), lower shrub intercept (10.1%, P=0.02), and greater angles of obstruction (18.5 degrees, P=0.005) than bobwhite diurnal locations; this may facilitate escape from nocturnal mammalian predators. Our results suggest that bobwhite escape strategies and cover use vary among threat types. These results support current management recommendations of creating a patchwork of vegetation covers for bobwhites but also suggest how a more complete understanding of bobwhite behavior would improve management and conservation efforts.

Journal of Wildlife Management↗
USGS2005

Effects of hunting on survival of American woodcock in the Northeast

Numbers of American woodcock ( Scolopax minor ) males counted on the annual singing ground survey (SGS) have declined over the last 35 years at an average rate of 2.3% per year in the Eastern Region and 1.8% per year in the Central Region. Although hunting was not thought to be a cause of these declines, mortality caused by hunters can be controlled. Furthermore, there has been no research on effects of hunting mortality on woodcock populations at local and regional levels on the breeding grounds. We used radiotelemetry to determine survival rates and causes of mortality for 913 woodcock captured during fall 1997–2000 on 7 areas in Maine, New Hampshire, Pennsylvania, and Vermont, USA. Three of 7 sites were closed to hunting. For all sites and all years combined, 176 woodcock died, and 130 were censored, of which 39 were censored mortalities. Predation was the major ( n = 134, 76%) cause of mortality. Mammals accounted for 56% of the predation, raptors accounted for 25%, and 19% was attributed to unknown predators. On hunted sites, 36% of the total mortality ( n = 102) was caused by hunting, 63% by predation, and 1 bird starved. Kaplan-Meier survival curves did not differ between hunted and non-hunted sites among years ( P = 0.46). Overall, point estimates of survival did not differ ( P = 0.217) between hunted (SR = 0.636, SE = 0.04) and nonhunted sites (SR = 0.661, SE = 0.08). We modeled hazard rates from hunting and natural mortality events using program MARK. Akaike's Information Criterion supported using a model with common constant hazards from both hunting and natural causes for groups of sites. Groupings of sites for hazard rates from natural causes were not influenced by whether a site was hunted or not. Models detected no effects of woodcock age and sex ( P = 0.52) on survival. Proportional hazards models comparing hunted and nonhunted sites found no effects of age and sex ( P = 0.45), interactions of age, sex, capture weight, and bill length ( P ≥ 0.269). Our data suggest that current hunting regulations are not causing lower survival of woodcock.

Maine, New Hampshire, Pennsylvania, Vermont↗