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We studied adult Cooper's hawks Accipiter cooperii on two study areas in north Florida from 1995 to 2001, an area dominated by large plantations managed for northern bobwhite Colinus virginianus and an area of mixed farmland and woods with no direct bobwhite management. We monitored 76 Cooper's hawk nesting attempts at 31 discrete nest areas, and radio-tagged 19 breeding males and 30 breeding females that we radio-tracked for up to 5 y. Nesting density (565 to 1,494 ha per occupied nest area) was comparable but productivity (1.8 and 2.8 young fledged per occupied and successful nest area, respectively) was lower than for the species elsewhere. Prey may have been more limiting than in other areas studied because chipmunks Tamias striatus, an important prey elsewhere, were absent. Annual Cooper's hawk survival averaged 84% for males and 81% for females, except in 1998 when survival was substantially lower. Average annual home-range size for male Cooper's hawks was 15.3 km2 inclusive of one nesting area. Female annual ranges averaged 30.3 km2, and included from three to nine nesting areas. Daily space use was similar between the sexes, but females had separate breeding and nonbreeding ranges whereas males were sedentary. Females used the same nonbreeding areas among years, but switched nesting areas 68% of the time compared with only 17% for males. Birds comprised 88% of the breeding and 98% of the nonbreeding season diet of Cooper's hawks by frequency. Important prey species all year were mourning doves Zenaida macroura, blue jays Cyanocitta cristata, and northern bobwhite; during summer, cattle egrets Bubulcus ibis, northern mockingbirds Mimus polyglottos and northern cardinals Cardinalis cardinalis were also important; and during autumn and winter, killdeer Charadrius vociferus, yellow-billed cuckoos Coccyzus americanus, and chickens were important. Female Cooper's hawks took larger prey than males; females were responsible for most cattle egret and chicken kills; whereas, males took most blue jays, killdeer, northern mockingbirds, and northern cardinals. Of avian prey brought to nests, 64% were nestling birds. Most adult male Cooper's hawks were adept at raiding bird nest boxes. Male Cooper's hawks captured 85% of the prey fed to nestlings. Female Cooper's hawks relied on males for food from early March until young were ≥12 d old, and 6 of 10 breeding females monitored intensively were never observed foraging for their broods. Most prey brought to nestling Cooper's hawks was captured within 2 km of nests, and foraging effort was consistent throughout the day. During the nonbreeding season, most prey captures occurred before 0900 hours or at dusk. Northern bobwhite made up 2% of male and 6% of female Cooper's hawk prey annually by frequency; this extrapolated to 18 bobwhite/year/adult Cooper's hawk on both study areas, 59% of which were captured between November and February. Outside the breeding season, male Cooper's hawks foraged evenly over their home range whereas females tended to focus on prey concentrations. Because female Cooper's hawks were so adept at finding and exploiting prey hotspots, perhaps the best strategy for reducing predation on bobwhite is habitat management that produces an even distribution of bobwhite across the landscape.
We studied adult Cooper's hawks Accipiter cooperii on two study areas in north Florida from 1995 to 2001, an area dominated by large plantations managed for northern bobwhite Colinus virginianus and an area of mixed farmland and woods with no direct bobwhite management. We monitored 76 Cooper's hawk nesting attempts at 31 discrete nest areas, and radio-tagged 19 breeding males and 30 breeding females that we radio-tracked for up to 5 y. Nesting density (565 to 1,494 ha per occupied nest area) was comparable but productivity (1.8 and 2.8 young fledged per occupied and successful nest area, respectively) was lower than for the species elsewhere. Prey may have been more limiting than in other areas studied because chipmunks Tamias striatus, an important prey elsewhere, were absent. Annual Cooper's hawk survival averaged 84% for males and 81% for females, except in 1998 when survival was substantially lower. Average annual home-range size for male Cooper's hawks was 15.3 km2 inclusive of one nesting area. Female annual ranges averaged 30.3 km2, and included from three to nine nesting areas. Daily space use was similar between the sexes, but females had separate breeding and nonbreeding ranges whereas males were sedentary. Females used the same nonbreeding areas among years, but switched nesting areas 68% of the time compared with only 17% for males. Birds comprised 88% of the breeding and 98% of the nonbreeding season diet of Cooper's hawks by frequency. Important prey species all year were mourning doves Zenaida macroura, blue jays Cyanocitta cristata, and northern bobwhite; during summer, cattle egrets Bubulcus ibis, northern mockingbirds Mimus polyglottos and northern cardinals Cardinalis cardinalis were also important; and during autumn and winter, killdeer Charadrius vociferus, yellow-billed cuckoos Coccyzus americanus, and chickens were important. Female Cooper's hawks took larger prey than males; females were responsible for most cattle egret and chicken kills; whereas, males took most blue jays, killdeer, northern mockingbirds, and northern cardinals. Of avian prey brought to nests, 64% were nestling birds. Most adult male Cooper's hawks were adept at raiding bird nest boxes. Male Cooper's hawks captured 85% of the prey fed to nestlings. Female Cooper's hawks relied on males for food from early March until young were ≥12 d old, and 6 of 10 breeding females monitored intensively were never observed foraging for their broods. Most prey brought to nestling Cooper's hawks was captured within 2 km of nests, and foraging effort was consistent throughout the day. During the nonbreeding season, most prey captures occurred before 0900 hours or at dusk. Northern bobwhite made up 2% of male and 6% of female Cooper's hawk prey annually by frequency; this extrapolated to 18 bobwhite/year/adult Cooper's hawk on both study areas, 59% of which were captured between November and February. Outside the breeding season, male Cooper's hawks foraged evenly over their home range whereas females tended to focus on prey concentrations. Because female Cooper's hawks were so adept at finding and exploiting prey hotspots, perhaps the best strategy for reducing predation on bobwhite is habitat management that produces an even distribution of bobwhite across the landscape.
Does breeding population trajectory and age of nesting females influence disparate nestling sex ratios in two populations of Cooper's hawks?
Offspring sex ratios at the termination of parental care should theoretically be skewed toward the less expensive sex, which in most avian species would be females, the smaller gender. Among birds, however, raptors offer an unusual dynamic because they exhibit reversed size dimorphism with females being larger than males. And thus theory would predict a preponderance of male offspring. Results for raptors and birds in general have been varied although population‐level estimates of sex ratios in avian offspring are generally at unity. Adaptive adjustment of sex ratios in avian offspring is difficult to predict perhaps in part due to a lack of life‐history details and short‐term investigations that cannot account for precision or repeatability of sex ratios across time. We conducted a novel comparative study of sex ratios in nestling Cooper's hawks (Accipiter cooperii) in two study populations across breeding generations during 11 years in Wisconsin, 2001–2011. One breeding population recently colonized metropolitan Milwaukee and exhibited rapidly increasing population growth, while the ex‐Milwaukee breeding population was stable. Following life‐history trade‐off theory and our prediction regarding this socially monogamous species in which reversed sexual size dimorphism is extreme, first‐time breeding one‐year‐old, second‐year females in both study populations produced a preponderance of the smaller and cheaper sex, males, whereas ASY (after‐second‐year), ≥2‐year‐old females in Milwaukee produced a nestling sex ratio near unity and predictably therefore a greater proportion of females compared to ASY females in ex‐Milwaukee who produced a preponderance of males. Adjustment of sex ratios in both study populations occurred at conception. Life histories and selective pressures related to breeding population trajectory in two age cohorts of nesting female Cooper's hawk likely vary, and it is possible that these differences influenced the sex ratios we documented for two age cohorts of female Cooper's hawks in Wisconsin.
Golf courses ostensibly offer green space in urbanized areas, but it is unclear how suitable these human‐modified habitats are for wildlife populations. Golf courses are home to a variety of wildlife, but in particular they have been the focus of research on avian responses to urbanization. Although numerous reproductive and diversity studies have been conducted on birds of golf courses, no research exists on postfledging survival in this created landscape. In 2008 and 2009, we estimated survival of eastern bluebird (Sialia sialis) fledglings using radio telemetry on golf course and other developed sites in Williamsburg, Virginia. We used nest survival models in Program MARK set in an information theoretic framework to assess whether the golf course habitat predicted mortality along with other previously studied variables, such as fledgling age, year, site, body condition, fledging date, and transmitter weight. We found no evidence that inhabiting a golf course increased mortality during the fledgling period, but we did find support for both fledgling age and fledging date as predictors of survival. Mortality decreased for older fledglings and those that fledged later in the season. Cause‐specific postfledging survival rates did not differ among sites. Fledgling bluebirds did, however, move into habitat that was significantly more forested and less grassy than their natal habitat. For managers of wildlife on golf courses and other urbanized sites, our study is the first to show that placing nest boxes in manicured habitat may attract birds to areas without suitable habitat for fledglings. © 2011 The Wildlife Society.
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