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Beninde and Cooper discuss the migration of Cooper's hawk (Accipiter cooperii) to urban territories. Having lost much of its former range in Southern California due to urbanization and persecution, the Cooper's hawk (Accipiter cooperii) shifted to urban territories and has since made a remarkable comeback in the 21st century. A cooperii is now widely distributed across the greater Los Angeles metropolitan area. Many pairs thrive by preying on some of the most widespread, cosmopolitan, urban-dwelling species, including non-native fox squirrels and rats. While Cooper's hawks are well known for preying on birds in natural habitats, the juvenile seen above is feeding on a non-native rat in a fully urbanized setting far from open space or native vegetation.

Wind energy development is advancing rapidly, but the potential ramifications of this growth on wildlife, particularly birds and bats, are not fully understood. Wind energy development may affect raptor (birds of prey) populations indirectly by displacing them from their previously occupied habitat; however, there are limited empirical data demonstrating this effect. We performed long-term raptor surveys at a wind farm previously implicated in the displacement of resident raptors and found that the duration of displacement varied among raptor species. Abundances of turkey vultures (Cathartes aura), red-tailed hawks (Buteo jamaicensis), and accipiters (sharp-shinned hawks [Accipiter striatus] and Cooper’s hawks [Accipiter cooperii] combined) all rebounded in years 7 and 8 of wind farm operation, while the apparent displacement of northern harriers (Circus hudsonius) and American kestrels (Falco sparverius) persisted across all post-construction monitoring periods. Our long-term assessment indicates not only that wind farm construction and operation may displace raptors but also that these impacts can diminish over time for certain species. This finding underscores the importance of assessing potential impacts over the operational life of a given wind farm and the need for long-term monitoring to validate predicted impacts, particularly for raptor communities.

Infectious diseases can cause host mortality through direct or indirect mechanisms, including altered behavior. Diminished anti-predator behavior is among the most-studied causes of indirect mortality during infection, particularly for systems in which a parasite’s life-cycle requires transmission from prey to predator. Significantly less work has examined whether directly-transmitted parasites and pathogens also reduce anti-predator behaviors. Here we test whether the directlytransmitted bacterial pathogen, Mycoplasma gallisepticum (MG), reduces responses to predation-related stimuli in house finches Haemorhous mexicanus. MG causes conjunctivitis and reduces survival among free-living finches, but rarely causes mortality in captivity, suggesting a role for indirect mechanisms. Wild-caught finches were individually housed in captivity and exposed to the following treatments: 1) visual presence of a stuffed, mounted predator (a Cooper’s hawk Accipiter cooperii) or control object (a vase or a stuffed, mounted mallard duck Anas platyrhynchos), 2) vocalizations of the same predator and non-predator, 3) approach of a researcher to enclosures, and 4) simulated predator attack (capture by hand). MG infection reduced anti-predator responses during visual exposure to a mounted predator and simulated predator attack, even for birds without detectable visual obstruction from conjunctivitis. However, MG infection did not significantly alter responses during human approach or audio playback. These results are consistent with the hypothesis that predation plays a role in MG-induced mortality in the wild, with reduced locomotion, a common form of sickness behavior for many taxa, as a likely mechanism. Our results therefore suggest that additional research on the role of sickness behaviors in predation could prove illuminating.

Social monogamy is the prevalent mating system in birds, but alternative strategies of extra‐pair paternity (EPP) and conspecific brood parasitism (CBP) occur in many species. Raptors are virtually absent in discussions of broad taxonomic reviews regarding EPP and CBP likely because these strategies are mostly absent or at low frequency; CBP is unreported in solitary nesting raptors. In contrast, we found high frequencies of EPP (16%–31%) and CBP (15%–26%) nests among three populations of Cooper's Hawks (Accipiter cooperii) across the northern breeding range of this solitary nesting, socially monogamous species. EPP and CBP combined occurred in 42%–46% of all nests among populations and hence unexpectedly were nearly equivalent to proportions of genetically monogamous nests. Select covariates failed to predict presence of EPP and CBP in part because virtually all extra‐pair adults were uncaught and likely were floaters. We found no support for the hypothesis that territorial females traded copulations for food to maximize energy intake for increased production. Our unique discoveries enhance knowledge of the extent and diversity of alternative breeding strategies among groups of avian and other animal species. Raptors are virtually absent in discussions of broad taxonomic reviews regarding extra‐pair paternity (EPP) and conspecific brood parasitism (CBP) likely because these strategies are mostly absent or at low frequency. In contrast, we found high frequencies of EPP (16%–31%) and CBP (15–26%) per nest among three populations of Cooper's Hawks (Accipiter cooperii) across the northern breeding range of this solitary nesting, socially monogamous species. Our unique discoveries enhance knowledge of the extent and diversity of alternative breeding strategies among groups of avian and other animal species.

Integrated population models (IPMs) combine population counts with demographic data to improve the precision of estimates of population size and demographic rates. IPMs can also provide information on demographic parameters for which data are lacking (e.g., immigration) if other sufficient information is available. IPMs often use demographic data from one sex, usually females, implicitly assuming the chosen sex adequately represents the species' life history; for highly size‐dimorphic raptors, that assumption may not hold true. We developed a two‐sex IPM for a New Mexico population of the highly size‐dimorphic Cooper's hawk (Accipiter cooperii) from 2011 to 2020 and compared estimates of life history characteristics between sexes. Because we had data to directly estimate sex‐ and age‐specific probabilities of breeding, fecundity, survival, brood sex ratios, and emigration rates, we could indirectly estimate age‐specific immigration rates for both sexes. Our two‐sex IPM revealed that population growth was most strongly associated with increased immigration and decreased first‐year (FY) emigration in females and with after‐first‐year (AFY) survival in males. Most males that were recruited as new breeders in our study area were AFY residents, whereas most female recruits were AFY immigrants. All females that fledged in our study area and survived until their first breeding season bred in their first year, whereas only 3% of surviving FY males bred. We found evidence of density dependence in the survival of AFY males (r = −0.11, 95% credible interval = −0.36 to −0.03) and in AFY female immigration (r = −0.17, 95% credible interval = −0.27 to −0.12). Our findings reveal that male and female Cooper's hawks differ in their response to population density, and in how they contribute to population growth. Thus, sexual differences in vital rates can be an important consideration in raptor population models.

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.

Cooper's Hawks (Accipiter cooperii) have been extending their breeding range into urban areas, prompting questions about the relative importance of cities to the demography and conservation of these raptors. A key unanswered question is how urban subpopulations interact with their precedent exurban subpopulations. Two general models have been proposed to describe relationships among subpopulations in a metapopulation: (1) source–sink, where immigrants from sources sustain sinks; and (2) balanced dispersal, where dispersal is proportionally equal among subpopulations. I evaluated whether either of these models predict metapopulation dynamics of urban and exurban Cooper's Hawks in central New Mexico using demographic data in a Bayesian integrated population model. All urban female Cooper's Hawks began breeding in their first year; 69% settled at nests in the urban subpopulation and 31% emigrated and settled in an exurban subpopulation. The high rate of female emigration was likely because of a shortage of breeding urban males, caused by a 1 yr delay in male age-at-first-breeding. Emigration exceeded immigration by nearly 30%, making a balanced-dispersal model implausible. Although the urban subpopulation was a source, the primary recipient subpopulation was not a sink; urban emigrants appeared to have a competitive advantage obtaining exurban nest sites. High urban winter prey abundance supported year-long residency among urban female Cooper's Hawks, whereas nearly all exurban females migrated. Resident urban females that emigrated settled on exurban nesting territories before migrants returned, and thus without direct competition from them. Previous metapopulation models do not incorporate the concept that differences in dispersal behavior between subpopulations can drive dispersal dynamics in a metapopulation. These findings provide further evidence that patch dynamics in a metapopulation can be complex, and may be governed by factors other than just demographic rates and connectivity.

Background Bird species worldwide are affected by trichomoniasis caused by the protist Trichomonas gallinae . In avivorous raptors such as Cooper’s hawks ( Accipiter cooperii ), nestlings are more susceptible than fledglings and adults. Previous research suggested a link between oral pH and susceptibility: the oral pH of fledgling and adult hawks is more than seven times more acidic than that of nestlings. We speculated that this age-specific difference in pH would correspond to age-specific differences in the oral microbiota of Cooper’s hawks. We examined the oral microbiomes of 31 healthy, wild Cooper’s hawks in Tucson, Arizona (USA). Individuals represented three age classes (nestlings, fledglings, and adults). We designed our study with multiple controls, replicated sampling, mock communities, and stringent quality-controls to address challenges that can limit the inferential quality of microbiome data sets. Results Richness of bacterial communities in oral cavities of Cooper’s hawks differed as a function of age but not as a function of sex, sampling date, or sampling location. Bacterial communities in oral cavities of nestlings differed from those of fledglings and adults, whereas communities in fledglings and adults did not differ from each other. Communities were similar in males and females and did not differ over the sampling season. Prevalence of acid-producing bacteria in fledgling and adults vs. nestlings is consistent with previous reports of age-specific variation in oral pH, but further research is needed to establish a causal link to pH levels or susceptibility to disease. Analyses of mock communities demonstrated high repeatability and showed that operon number and read abundance were highly correlated. Conclusions The oral microbiota of wild Cooper’s hawks differs between nestlings and older birds. Variation in the oral microbiome is consistent with differences in oral pH between nestlings and older individuals. Overall our study provides a first perspective on bacterial communities associated with oral cavities of a wild raptor.

Bird banding has allowed us to understand diverse aspects of the life histories of migratory raptors. However, most banding stations are located at northern latitudes so what we know about the movements of these raptors is biased toward higher latitudes, primarily from Canada and the United States, leaving important gaps in our knowledge of their movements at lower latitudes. Our objective was to describe the migratory movements of Sharp-shinned (Accipiter striatus) and Cooper’s (A. cooperii) hawks based on banding and recapture records of birds that migrate through Veracruz, Mexico. More specifically, we sought to determine their breeding, migration, and non-breeding locations, estimate their migration distances, and contribute to a better understanding of their migration patterns. With a total of 80 records, we calculated migration distances and used Kernel Density Estimation analyses to identify where these hawks were recaptured or recovered by season. The distribution of recaptures and recoveries largely coincided with breeding locations in the Laurentian Upland and the Interior Plains physiographic regions. All migration records follow a trajectory that extends from the midwestern United States to the Gulf coastal plain of Mexico. The mean breeding season migration distance to Veracruz was 3374 km (a difference of 27 degrees of latitude) for Sharp-shinned Hawks and 2926 km (a difference of 25 degrees of latitude) for Cooper’s Hawks. Our non-breeding records indicate that populations of Accipiter hawks from these North American populations migrate the longest distances to reach Central America, the southernmost distribution of their migratory populations. Distances covered by both species represent round-trip migrations that may be as long as 10,000 km. Our results support those of previous studies and illustrate how continental physiography influences the migration routes, migratory behavior, and migratory connectivity of these hawks. El anillamiento de aves ha permitido comprender diversos aspectos de la historia de vida de las rapaces migratorias. Sin embargo, la mayoría de las estaciones de anillado está en latitudes norteñas, por lo que lo sabido de sus movimientos está sesgado a mayores latitudes, principalmente de Canadá y los Estados Unidos, dejando importantes vacíos en nuestro conocimiento de sus movimientos a menores latitudes. En este estudio describimos los movimientos migratorios de los gavilanes Accipiter striatus y A. cooperii por medio de registros de anillado y recaptura de individuos que migran por Veracruz, México. Nuestra meta fue determinar sus localidades de reproducción, migración y no-reproductivas, estimar su distancia de migración y contribuir al entendimiento de sus patrones de migración. Con un total de 80 registros, calculamos las distancias de migración, usamos análisis de Estimacion de Densidad de Kernel para identificar las regiones donde se concentran las recapturas por temporada. La distribucion de las recapturas y reencuentros de anillos coincidió en su mayoría con localidades de origen en las regiones fisiográficas Meseta Laurentiana y Planicies del Interior. Todos los registros de migracion siguen una trayectoria que extiende desde el medio-oeste de los Estados Unidos hasta la planicie costera del Golfo de Mexico. La distancia media de migracion a Veracruz para A. striatus es de 3374 km (una diferencia de 27 grados de latitud), mientras que aquella de A. cooperii es de 2926 km (una diferencia de 25 grados de latitud). Nuestros registros de la temporada no-reproductiva indicaron que las poblaciones de estas poblaciones de Norteamérica migran las mayores distancias para llegar a Centroamerica, la región más austral de la distribucion de sus poblaciones migratorias. Las distancias cubiertas por ambas especies representan migraciones que pueden llegar a los 10,000 km de ida y vuelta. Nuestros resultados apoyan otras investigaciones previas que ilustran cómo la fisiografia es un factor determinante en la definición de rutas migratorias, el comportamiento y la conectividad migratoria de estos gavilanes.

We assessed total mercury (THg) concentrations in breast feathers of diurnal North American raptors collected at migration monitoring stations. For 9 species in the Pacific Flyway, we found species and age influenced feather THg concentrations whereas sex did not. Feather THg concentrations µg/g dry weight (dw) averaged (least squares mean ± standard error) higher for raptors that generally consume > 75% avian prey (sharp-shinned hawk Accipiter striatus: n = 113; 4.35 ± 0.45 µg/g dw, peregrine falcon Falco peregrinus: n = 12; 3.93 ± 1.11 µg/g dw, Cooper’s hawk Accipiter cooperii: n = 20; 2.35 ± 0.50 µg/g dw, and merlin Falco columbarius: n = 59; 1.75 ± 0.28 µg/g dw) than for raptors that generally consume < 75% avian prey (northern harrier Circus hudsonius: n = 112; 0.75 ± 0.10 µg/g dw, red-tailed hawk Buteo jamaicensis: n = 109; 0.56 ± 0.06 µg/g dw, American kestrel Falco sparverius: n = 16; 0.57 ± 0.14 µg/g dw, prairie falcon Falco mexicanus: n = 10; 0.41 ± 0.13 µg/g dw) except for red-shouldered hawks Buteo lineatus: n = 10; 1.94 ± 0.61 µg/g dw. Feather THg concentrations spanning 13-years (2002–2014) in the Pacific Flyway differed among 3 species, where THg increased for juvenile northern harrier, decreased for adult red-tailed hawk, and showed no trend for adult sharp-shinned hawk. Mean feather THg concentrations in juvenile merlin were greater in the Mississippi Flyway (n = 56; 2.14 ± 0.18 µg/g dw) than those in the Pacific Flyway (n = 49; 1.15 ± 0.11 µg/g dw) and Intermountain Flyway (n = 23; 1.14 ± 0.16 µg/g dw), and Atlantic Flyway (n = 38; 1.75 ± 0.19 µg/g dw) averaged greater than the Pacific Flyway. Our results indicate that raptor migration monitoring stations provide a cost-effective sampling opportunity for biomonitoring environmental contaminants within and between distinct migration corridors and across time.