Nesting Biology of Urban Cooper’s Hawks in Alameda County, California

In recent decades Cooper’s Hawks have successfully colonized urban landscapes, where there may be ample prey but also a greater prevalence of disease in their prey. We searched for nesting Cooper’s Hawks in and around Berkeley, California, from 2002 to 2010, locating 95 nests, 89 of which successfully fledged at least one nestling. On average, each nest produced 3.6 fledglings. We evaluated the possible effects of the protozoan parasite Trichomonas gallinae on Cooper’s Hawk reproduction from the proportion of potential prey items brought to Lindsay Wildlife Experience that tested positive for the parasitic disease. We did not find a correlation between T. gallinae in potential prey species and nest success (i.e., if the nest fledged any offspring) or reproductive success (i.e., number of fledglings produced). Similarly, we did not find a relationship between reproductive success and distance to parks or percent of impervious surface within 500 m of the nest. The high reported rates of reproduction and high densities of Cooper’s Hawk in Berkeley and neighboring Albany suggest a robust population, and we did not find evidence that T. gallinae influences its reproductive success.

Riding the storm out: select demographics of a breeding population of Cooper’s hawks (Accipiter cooperii) following a severe spring snowstorm

The demographic responses to severe weather by top-level predators, including birds of prey, are underreported and/or unknown. Severe storms are predicted by climate change models to increase globally and in frequency into the 22nd century. In April 2018, a population of breeding Cooper’s hawks (Accipiter cooperii) in central Wisconsin, USA, experienced three days of heavy snowfall in the most severe storm, in pre-incubation-stage, for 39 years (1980–2018). Here I report select demographic outcomes of this nesting population following this intense weather. The median hatching date of 10 June in 2018 was the sixth latest such metric in those 39 years (and the latest in 22 years since 1996) for this population, which has advanced its breeding schedule about 1.3 days/decade due to climate change or warming. Survival of a total of 16 color-marked breeding adults, 15 males and 1 female, observed pre-storm in the nesting areas, was 100% up through the late nestling stage in the same nesting areas where these birds were initially detected in 2018. Average clutch size (4.4 eggs/nest) and average brood size (4.0 young/nest) were similar to the overall average annual metrics of these demographics for this population in the earlier 38 study years. Nest success, whereby 95% of 21 nests with eggs produced advanced-aged young, was higher in 2018 than the overall average of 77% nest success rate during the earlier years. The later timing of hatching in 2018, likely due to the severe spring snowstorm, appeared to have no deleterious effects either on survival of the breeding adults or on the reproductive output of this healthy study population. Tree-canopy prey may have served as important alternative food for this typically ground-foraging raptor in 2018.

Demographic consequences of sexual differences in age at first breeding in Cooper’s Hawks (Accipiter cooperii)

Life-history theory predicts individuals should breed as soon as they are able to reproduce, but many long-lived birds delay breeding. In the Accipitriformes, delayed breeding is the norm, and age when breeding begins is influenced by competing selective pressures. In most Accipitriformes, the reproductive roles of males and females differ; males do most of the foraging and females tend eggs and young. Thus, sexual differences in age at first breeding might be expected, but these differences, possible causes, and implications for individual fitness have received little study. We investigated sexual differences in age at first breeding in a marked population of Cooper’s Hawks (Accipiter cooperii) from 2011 through 2018 in central New Mexico, USA. We hypothesized that males required more experience to pair and breed successfully than females, and we predicted: (1) a lower mean age at first breeding for females than males, and (2) that expected individual fitness of early-breeding males would be lower than for early-breeding females. We found that 79% more females than males bred in their first year (hatching year, HY), and expected individual fitness of HY-breeding females was 21% greater than for HY-breeding males. HY males that attempted to breed settled on nesting territories with exceptionally high prey abundance, nevertheless they experienced 37% lower second-year survival than males that delayed breeding. Females competed for mates based on male age. HY females that paired with relatively older males had 33% higher second-year survival and 16% higher expected individual fitness than HY females that initially paired with relatively younger males. The observed annual rate of growth (λ) of our study population was 1.08, closer to λ predicted by male (1.02) than female (1.21) demographic models. Delayed breeding by males thus had important ramifications for λ, highlighting the need to consider sexual differences in age at first breeding in demographic analyses.