Nesting Biology of Urban Cooper's Hawks in Milwaukee,Wisconsin

ABSTRACT Urban landscapes vary greatly across North America and long-term data on the nesting biology of Cooper's hawks (Accipiter cooperii) from a variety of urban environments will improve our understanding of these poorly studied populations. We studied Cooper's hawks nesting in the metropolitan Milwaukee area, Wisconsin, USA, over a 12-year period, 1993–2004. Nesting success for 254 first nesting attempts averaged 64.6% with means of 2.27 young per laying pair and 3.53 young per successful pair. For 8 second nesting attempts (i.e., re-nests), nesting success averaged 87.5% with means of 2.57 young per laying pair and 3.00 young per successful pair. Productivity for first nesting attempts did not vary over the 12-year period, and productivity for re-nests did not differ from first nesting attempts. We documented evidence of nest predation by raccoons (Procyon lotor) and red-tailed hawks (Buteo jamaicensis). On average, second year (SY [i.e., 1-yr-old]) Cooper's hawks comprised 14.6% (43 of 295 breeding birds; 21.5% [37 of 172] of F and 4.9% [6 of 123] of M) of the known breeding population. The percentage of SY breeders within this population declined over the 12-year period, suggesting a relatively young population. Cooper's hawks consistently reoccupied nest sites annually after initial discovery over an estimated 2 generations of breeding adults, suggesting that population density for our study was at least stable. We trapped 105 breeding adults, including 5 natal dispersal birds. Based on long-term, relatively high reproduction, repeated re-occupancy of nest sites, and confirmed recruitment from within this population, we suggest that these nesting areas were not marginal or inferior habitats and that urban Cooper's hawks in this study area were not a sink population. We recommend no active management of this population at this time; however, additional information for nesting Cooper's hawks from other urban environs will expand our knowledge base for these populations.     

Buteo Nesting Ecology: Evaluating Nesting of Swainson’s Hawks in the Northern Great Plains

Swainson’s hawks (Buteo swainsoni) are long-distance migratory raptors that nest primarily in isolated trees located in areas of high grassland density. In recent years, anthropogenic conversion of grassland habitat has raised concerns about the status of the breeding population in the northern Great Plains. In 2013, we initiated a study to investigate the influence of extrinsic factors influencing Swainson’s hawk nesting ecology in north-central South Dakota and south-central North Dakota. Using ground and aerial surveys, we located and monitored nesting Swainson’s hawk pairs: 73 in 2013 and 120 in 2014. We documented 98 successful breeding attempts that fledged 163 chicks; 1.52 and 1.72 fledglings per successful nest in 2013 and 2014, respectively. We used Program MARK to evaluate the influence of land cover on nest survival. The top model, S _{Dist2Farm+%Hay}, indicated that nest survival (fledging at least one chick) decreased as nests were located farther from farm sites and as the percent of hay cover increased within 1200-m of the nest site (34.4%; 95% CI = 27.6%–42.3%). We used logistic regression analysis to evaluate the influence of landscape variables on nest-site selection; Swainson’s hawks selected for nest sites located closer to roads. We suggest that tree belts associated with farm sites, whether occupied or not, provide critical breeding sites for Swainson’s hawks. Additionally, poor breeding success may be related to the late migratory behavior of this species which requires them to occupy marginal habitat due to other raptors occupying the most suitable habitat prior to Swainson’s hawks arriving to the breeding grounds.     

Site occupancy and cavity use by the northern flying squirrel in the boreal forest

Tree cavities are used as shelter and breeding nests by numerous avian and mammalian species. In cold environments, tree cavities are often proposed as the best winter nest choice because of the superior protection they offer from precipitation, wind, cold temperatures, and predators. As such, they represent a critical resource, which has the potential to limit population size of non-excavating species. We assessed factors affecting site occupancy in the boreal forest by northern flying squirrels, a secondary user of tree cavities, and to identify which nest type is preferred during the colder days of the autumn–winter period. We trapped flying squirrels twice in 59 aspen-dominated stands in the autumn period using low- (1.5 m above ground-level) and high-mounted (4 m) traps to determine site occupancy. A total of 85 individuals were captured on 2,880 trap-nights. During the winter period, we radio-tracked 26 individuals to 87 diurnal nests in 220 locations. None of the habitat variables considered (cavity availability, woody debris, and lateral cover) explained site occupancy. Detectability decreased with precipitation, and was lower using high traps than low traps. Both females and males used tree cavities (26%), external nests (39%), and ground nests (35%). In cold weather, females preferred ground nests, whereas males preferred external nests. Our results do not support the hypothesis that tree cavities represent a limiting factor to northern flying squirrels in cold environments. Instead, this species seems to be a generalist and is opportunistic, using a variety of nest types. Nevertheless, practices ensuring the persistence of large diameter live cavity trees, providing better insulative properties, are likely to increase the relative use of tree cavities as nest sites by northern flying squirrels. © 2011 The Wildlife Society.     

Microhabitat nest‐site selection by ducks in the boreal forest

The boreal forest is one of the North America’s most important breeding areas for ducks, but information about the nesting ecology of ducks in the region is limited. We collected microhabitat data related to vegetation structure and composition at 157 duck nests and paired random locations in Alberta’s boreal forest region from 2016 to 2018. We identified fine‐scale vegetation features selected by ducks for all nests, between nesting guilds, and among five species using conditional logistic regression. Ducks in the boreal forest selected nest sites with greater overhead and graminoid cover, but less forb cover than random sites. Characteristics of the nest sites of upland‐ and overwater‐nesting guilds differed, with species nesting in upland habitat selecting nests that provided greater shrub cover and less lateral concealment and species nesting over water selecting nests with less shrub cover. We examined the characteristics of nest sites of American Wigeon (Mareca americana), Blue‐winged Teal (Spatula discors), Green‐winged Teal (Anas crecca), Mallards (Anas platyrhynchos), and Ring‐necked Ducks (Aythya collaris), and found differences among species that may facilitate species coexistence at a regional scale. Our results suggest that females of species nesting in upland habitat selected nest sites that optimized concealment from aerial predators while also allowing detection of and escape from terrestrial predators. Consequently, alteration in the composition and heterogeneity of vegetation and predator communities caused by climate change and industrial development in the boreal forest of Canada may affect the nest‐site selection strategies of boreal ducks.     

Nesting Habitat of the Lilac-crowned Parrot in a Modified Landscape in Mexico

Parrot populations are being increasingly pressured to occupy modified or fragmented landscapes, yet little is known of the habitat requirements of most species, particularly with regard to the effects on breeding habitat. We evaluated nesting habitat of the lilac-crowned parrot Amazona finschi in the modified landscape of coastal Michoacan in Mexico. We located 90 parrot nests in 12 tree species in Michoacan, with lilac-crowned parrots presenting a narrow niche-breadth of tree species used for nesting. Considering an additional 82 nest trees recorded for lilac-crowned parrots in Jalisco, we determined a 51 percent similarity in cavity resource use by parrots in the two dry forest regions. Overall, the predominant nest tree species with 76 percent of nests were Astronium graveolens , Piranhea mexicana , Brosimum alicastrum , and Tabebuia spp., all characteristic of semi-deciduous forest. Only 8 percent of nests occurred in trees characteristic of deciduous forest. Parrots utilized large trees with canopy level cavities as nest sites, and preferred conserved semi-deciduous forest for nesting, with fewer nests than expected in deciduous forest and transformed agricultural land. Nest areas in semi-deciduous forest occurred on significantly steeper terrain, as remnant semi-deciduous forest is restricted to steep ridges and canyons. Those parrot nests in modified habitats and forest patches were located near to continuous forest, with nest trees in open agricultural land being significantly closer to continuous forest than nests in disturbed forest patches. These results demonstrate the importance of conserved semi-deciduous forest as breeding habitat for the threatened, endemic lilac-crowned parrot, making wild populations of the species vulnerable to the high rate of transformation and fragmentation of tropical dry forest.     

Effect of Japanese lesser sparrowhawks Accipiter gularis on the nest site selection of azure-winged magpies Cyanopica cyana through their nest defending behavior

The frequency of azure-winged magpies Cyanopica cyana that nest in association with breeding Japanese lesser sparrowhawks Accipiter gularis was compared between the 1990s and 2000s. During 1990–1994 azure-winged magpies nested within 50 m of their nests in all of the hawk nest sites studied. During 2005–2006, however, the magpies nested in only two of nine hawk nest sites. During the 1990s Japanese lesser sparrowhawks chased jungle crows away when they intruded within 50 m of their nest. During the 2000s, on the other hand, the hawks attempted to expel few crows at a distance of more than 10 m from their nest. As a result of it, the predation rate of simulated magpie nests located in the hawk nest sites was significantly higher during the 2000s. This suggests that the magpies have the ability to assess the defending behavior of the hawks and judge whether they can rely on their defense. Most azure-winged magpies may stop nesting in association with breeding Japanese lesser sparrowhawks because of the reduced defending range of their nest sites.     

Old nests are cues for suitable breeding sites in the Eurasian penduline tit Remiz pendulinus

Nest-sites often have a major influence on avian reproductive success. The use of reliable cues that assist nest-site selection should thus be favoured by natural selection. The old nests have been known to serve as a cue in nest-site selection in several species. To find out whether the old nests act as cue in nest-site selection in the Eurasian penduline tit Remiz pendulinus , we carried out two experiments in southern Hungary, where the penduline tits breed around fishponds and build sophisticated pendulous nests on tree branches that often hang over water. In April 2006, we choose 20 groups of two nearby trees, and hung an old nest on one of the trees in each group. The male penduline tits choose 12 of these groups to build a new nest, and every of the twelve nests were built on trees with an old nest. This suggests that the old nests serve as a cue in the selection of breeding sites for males when they enter a habitat. To find out whether the old nests are cues of plentiful nest building material, or to signal high quality breeding areas, we carried out a second experiment in 2007 by selecting 13 groups of three nearby trees. A "worn-out" old nest was hung on one of the trees, a "re-utilize" type of old nest on another tree, whereas the third tree was left without an old nest in each group. The rationale was that while the worn-out material of the old nests is of no use in building the new nests, material of the "re-utilize" nests is good enough to be used for building new nests. Males built a new nest in 10 of the 13 groups, and eight of the new nests were built on trees with an old nest. Of the eight new nests, five were built on trees with a "worn-out" old nest and three on trees with a "re-utilize" type of old nest. It appears that for the penduline tit males it is the presence of an existing old nest and not the quality of the old nest material that serves as cue during the selection of the suitable breeding sites.     

Nest site selection and patterns of nest re-use in the Hooded Crow Corvus cornix

Capsule: Hooded Crows Corvus cornix selected nesting trees based on species, height, grouping and distance from an occupied house. Nest re-use was common and pairs that re-used old nests produced more fledglings than those that built a new nest.

Aims: To determine the features of trees that influenced whether they were used by Hooded Crows as nest sites, to establish what factors influenced nest re-use between years and to explore potential costs or benefits of nest re-use.

Methods: In a large area of Orkney, Scotland, the features of trees that contained a Hooded Crow nest were compared to those of trees where nests were absent. Patterns of nest re-use between years were examined in relation to the availability of alternative sites, previous nesting success and the number of equivalent options to the tree used previously within 200?m of this site.

Results: Hooded Crows favoured spruce and pine trees as nest sites, above the most locally abundant tree species, elder and willow. Preference for trees increased with tree height, local tree density and distance from occupied houses. Over half of the crows studied re-used an old nest when one was available and crows that re-used an old nest fledged more offspring than those that built a new nest. The likelihood of a new nest being built increased as the number of potential locations to build increased. Territories where a nest survived the winter were more likely to be reoccupied the following year than those where nests fell, while territories with fewer trees around the old site were most likely to be abandoned, suggesting that those were territories of lower quality.

Conclusions: Hooded Crows displayed strong preferences for nest sites that might favour nesting success by offering concealment, shelter and protection from ground-based predators. Nest re-use was common, especially when alternative sites were scarce, and appeared to facilitate greater reproductive output.     

Role of exotic tree stands on the current distribution and social behaviour of Swainson's hawk, Buteo swainsoni in the Argentine Pampas

Aim The Argentine Pampas was extensively and abruptly altered by European colonization. Between 1880 and 1885 the indigenous human inhabitants were completely displaced, and native grasslands were replaced by exotic pasture plants and crops. One of the most important ecological changes in the Pampas landscape, the introduction of tall exotic tree species, has received little attention, and its effect on wildlife has never been assessed. We have made an intensive survey of habitat use of Swainson's hawk, Buteo swainsoni in its most important non‐breeding quarters, the Pampas of Argentina, aiming to characterize the sites used by hawks for communal roosting. Location Pampas grasslands, Argentina. Methods We surveyed 30,000 km of roads by car during the austral summer from 2001 to 2004, covering the main non‐breeding area occupied by Swainson's hawks. Their roost sites were located by direct observation of birds roosting in tree stands close to the roads, by surveying potential roost sites around places where groups of pre‐ and post‐roosting hawks were recorded, and by gathering information from local farmers. Results Swainson's hawks exclusively used stands of exotic tree species for roosting. Eucalyptus viminalis was present in all 34 roosts surveyed, and in 59% of them it was the only species present. The remaining exotic tree species were the Siberian elm, Ulmus pumila, pines (Pinus spp.) and cypress (Cupressus spp.). Flock sizes at roost sites were unusually high for a raptor, with an average of 658 individuals (range 8–5000 hawks, n = 27 flocks). Main conclusions The introduction of exotic trees may have resulted in the expansion of the suitable habitat for Swainson's hawks, permitting a recent colonization of the Argentine Pampas. Tree stands may have also changed the communal roosting behaviour of this raptor, by virtue of their providing new structural elements in a region that almost completely lacked trees prior to European occupation.     

Nesting habitat characteristics of Marbled Murrelets occurring in near‐shore waters of the Olympic Peninsula,Washington

Marbled Murrelets (Brachyramphus marmoratus) are listed as threatened in the portion of their range extending from British Columbia to California due to loss of nesting habitat. Recovery of Marbled Murrelet populations requires a better understanding of the characteristics of their nesting habitat in this part of their range. Our objective, therefore, was to describe their nesting habitat in Washington State and Vancouver Island, British Columbia. We captured Marbled Murrelets from 2004 to 2008, fitted them with radio transmitters, and followed them to nests (N = 20). We used Cohen's unbiased d effect size to assess differences between forest plots surrounding nest sites and nearby control sites (N = 18). Nest sites had less canopy cover of the dominant conifers and fewer, but larger, trees than control sites. Nest sites also had greater percentages of trees with platforms >10 cm diameter and >15 cm diameter, and more platforms of these sizes than control sites. The mean diameter at breast height of nest trees was 136.5 cm (range = 84–248 cm) and all but one nest was in dominant or co‐dominant tree species. At the landscape scale, we used vegetation maps derived from remotely sensed data and found greater canopy cover, higher density of mature trees, more platforms >10 cm/ha, and more old‐growth habitat at nest sites than at random sites. Our findings suggest that, at the site scale, nesting Marbled Murrelets selected the most suitable features of forest structure across expansive potentially suitable habitat. Our landscape‐scale analysis showed that habitat features in nesting stands differed from those features in available stands in the murrelet's range in Washington. We also found that stands with nests were less fragmented than available forest across murrelet range. All nest sites of radio‐tagged birds in Washington were in protected areas in mostly undisturbed forest habitat. Conservation of these areas of inland nesting habitat will be critical to the recovery of Marbled Murrelet populations.     

The role of conservative versus innovative nesting behavior on the 25‐year population expansion of an avian predator

Species ranges often change in relation to multiple environmental and demographic factors. Innovative behaviors may affect these changes by facilitating the use of novel habitats, although this idea has been little explored. Here, we investigate the importance of behavior during range change, using a 25‐year population expansion of Bonelli's eagle in southern Portugal. This unique population is almost exclusively tree nesting, while all other populations in western Europe are predominantly cliff nesting. During 1991–2014, we surveyed nest sites and estimated the year when each breeding territory was established. We approximated the boundaries of 84 territories using Dirichlet tessellation and mapped topography, land cover, and the density of human infrastructures in buffers (250, 500, and 1,000 m) around nest and random sites. We then compared environmental conditions at matching nest and random sites within territories using conditional logistic regression, and used quantile regression to estimate trends in nesting habitats in relation to the year of territory establishment. Most nests (>85%, n = 197) were in eucalypts, maritime pines, and cork oaks. Nest sites were farther from the nests of neighboring territories than random points, and they were in areas with higher terrain roughness, lower cover by agricultural and built‐up areas, and lower road and powerline densities. Nesting habitat selection varied little with year of territory establishment, although nesting in eucalypts increased, while cliff nesting and cork oak nesting, and terrain roughness declined. Our results suggest that the observed expansion of Bonelli's eagles was facilitated by the tree nesting behavior, which allowed the colonization of areas without cliffs. However, all but a very few breeding pairs settled in habitats comparable to those of the initial population nucleus, suggesting that after an initial trigger possibly facilitated by tree nesting, the habitat selection remained largely conservative. Overall, our study supports recent calls to incorporate information on behavior for understanding and predicting species range shifts.     

Nest‐site selection by Slender‐billed Parakeets in a Chilean agricultural‐forest mosaic

ABSTRACT Species in the family Psittacidae may be particularly vulnerable to anthropogenic habitat transformations that reduce availability of suitable breeding sites at different spatial scales. In southern Chile, loss of native forest cover due to agricultural conversion may impact populations of Slender‐billed Parakeets (Enicognathus leptorhynchus), endemic secondary cavity‐nesting psittacids. Our objective was to assess nest‐site selection by Slender‐billed Parakeets in an agricultural‐forest mosaic of southern Chile at two spatial scales: nest trees and the habitat surrounding those trees. During the 2008–2009 breeding seasons, we identified nest sites (N= 31) by observing parakeet behavior and using information provided by local residents. Most (29/31) nests were in mature Nothofagus obliqua trees. By comparing trees used for nesting with randomly selected, unused trees, we found that the probability of a tree being selected as a nest site was positively related to the number of cavity entrances, less dead crown, and more basal injuries (e.g., fire scars). At the nesting‐habitat scale, nest site selection was positively associated with the extent of basal injuries and number of cavity entrances in trees within 50 m of nest trees. These variables are likely important because they allow nesting parakeets to minimize cavity search times in potential nesting areas, thereby reducing energetic demands and potential exposure to predators. Slender‐billed Parakeets may thus use a hierarchical process to select nest sites; after a habitat patch is chosen, parakeets may then inspect individual trees in search of a suitable nest site. Effective strategies to ensure persistence of Slender‐billed Parakeets in agricultural‐forest mosaics should include preservation of both individual and groups of scattered mature trees.     

Characteristics of Mount Graham Red Squirrel Nest Sites in a Mixed Conifer Forest

Abstract: The Mount Graham red squirrel (Tamiasciurus hudsonicus grahamensis) is constrained to the Pinaleño Mountains in southeastern Arizona, USA. The population's endangered status and extensive forest damage from insects and fire warrants a better understanding of habitat variables important for nest site selection. We examined characteristics of cavity (n = 91) and drey (n = 38) nests and compared these to random sites (n = 113). Dreys were found primarily in Engelmann spruce (Picea engelmannii) and corkbark fir (Abies lasiocarpa var. arizonica). Cavity nests occurred primarily in aspen (Populus tremuloides) and corkbark fir. Squirrels selected nest sites with higher canopy cover and more corkbark fir, decayed logs, and living trees. Forest management plans emphasizing thinning must consider how altering these habitat characteristics could affect availability and suitability of tree stands for nesting squirrels.     

Herbaceous ground cover reduces nest predation in olive groves

Capsule Bare ground increases artificial nest predation in olive groves.

Aims To assess the effect of different soil management regimes on nest predation rates in olive groves.

Methods We performed nest predation experiments with artificial nests during the breeding season in 2013, in two areas of southern Spain. Each artificial nest (n?=?300) contained three quail Coturnix eggs, two of which were unmanipulated and the third one was emptied and injected with plaster. Predators were identified by marks on eggs filled with plaster.

Results Ground nests were significantly more depredated, irrespective of the presence of ground cover; tree nests were less depredated in fields with ground cover. There was a clear difference in nest predators of ground and tree nests. Rodents were the most frequent predators of tree nests.

Conclusion Lower predation rates of tree nests in orchards with ground cover are probably linked to a change in the foraging behaviour of rodents, which in these more complex habitats might be restricted by rodents' own risk of predation. This study underscores the important role of agricultural practices in preserving farmland bird communities, particularly tree-nesting species, suggesting that for this group, implementation of ground cover in olive groves might enhance breeding success by reducing nest predation rates.     

Compounding effects of habitat fragmentation and predation on bird nests

Habitat fragmentation and invasive species are two of the greatest threats to species diversity worldwide. This is particularly relevant for oceanic islands with vulnerable endemics. Here, we examine how habitat fragmentation influences nest predation by Rattus spp. on cup‐nesting birds in Samoan forests. We determined models for predicting predation rates by Rattus on artificial nests at two scales: (i) the position of the bird's nest within the landscape (e.g. proximity to mixed crop plantations, distance to forest edge); and (ii) the microhabitat in the immediate vicinity of the nest (e.g. nest height, ground cover, slope). Nest cameras showed only one mammal predator, the black rat (Rattus rattus), predating artificial nests. The optimal model predicting nest predation rates by black rats included a landscape variable, proximity to plantations and a local nest site variable, the percentage of low (<15 cm) ground cover surrounding the nest tree. Predation rates were 22 ± 13% higher for nests in forest edges near mixed crop plantations than in edges without plantations. In contrast, predation rates did not vary significantly between edge habitat where the matrix did not contain plantations, and interior forest sites (>1 km from the edge). As ground cover reduced, nest predation rates increased. Waxtags containing either coconut or peanut butter were used as a second method for assessing nest predation. The rates at which these were chewed followed patterns similar to the predation of the artificial nests. Rural development in Samoa will increase the proportion of forest edge near plantations. Our results suggest that this will increase the proportion of forest birds that experience nest predation from black rats. Further research is required to determine if rat control is needed to maintain even interior forest sites populations of predator‐sensitive bird species on South Pacific islands.     

Estimation of Species Identification Error: Implications for Raptor Migration Counts and Trend Estimation

Abstract: One of the primary assumptions associated with many wildlife and population trend studies is that target species are correctly identified. This assumption may not always be valid, particularly for species similar in appearance to co-occurring species. We examined size overlap and identification error rates among Cooper's (Accipiter cooperii) and sharp-shinned (A. striatus) hawks specific to a raptor migration count station along the Pacific Coast of North America. Illustrating the difficulty of distinguishing between these 2 species, we found overlap in 7 metrics among species-sex groups and in 2 metrics between species, and a principal components analysis revealed a continuum of discrete clusters for each species-sex combination in morphospace. Among juvenile hawks (n = 940), we found the greatest misidentification rate for male Cooper's hawks (23% of the 156 males were identified as sharp-shinned), lesser error rates for female Cooper's (8%, n = 339) and female sharp-shinned (6%, n = 246), and the lowest misidentification rate for male sharp-shinned hawks (0%, n = 199). We observed a similar pattern of misidentification among adult hawks (n = 48). We attempted to use conditional probabilities (identification rates) from calibration data to calculate the true number of adult and juvenile Cooper's hawks and sharp-shinned hawks. Discrepancies between total number of observed accipiters and estimated number using calibration data suggest that daily observer misclassification rates are higher than misclassification rates estimated from calibration data and prevent correction of the raw data. Our results illustrate the importance of testing for and quantifying observer error in species identification in wildlife census and population trend studies particularly when target species may be easily confused with other nontarget species.     

Fragmentation in eucalypt woodlands promotes nest‐tree occupancy by a despotic species,the noisy miner (Manorina melanocephala)

The effects of habitat fragmentation as a threat to biodiversity are well known; decreased connectivity can potentially influence population processes and dynamics, resulting in smaller, isolated populations that may not function optimally. However, fragmentation may also increase the amount of edge or ecotone habitat available to open country species, benefiting their populations and enabling them to dominate remnant habitats. Noisy miners (Manorina melanocephala) are one such species, occupying eastern‐Australian eucalypt woodlands. They are considered a ‘despotic’ species, in that their presence negatively impacts woodland avifauna biodiversity due to their aggressive exclusion of other taxa from occupied areas. Despite this well‐known impact, little information exists on the patterns of nest‐tree occupancy by noisy miners within eucalypt woodlands. In the current study, we explored the patterns of nest‐tree occupancy by noisy miners across two successive years, aiming to identify preferences for breeding areas relative to vegetation structure. Our results show that both habitat fragmentation and the characteristics of individual eucalypt trees in an area influenced nest‐tree occupancy. Noisy miners constructed nests in trees near the edge of woodland patches more often than expected. Moreover, the nest tree chosen was a eucalypt that was significantly smaller than randomly selected trees from the surrounding area. The results highlight the importance of habitat management measures that may reduce the suitability of woodland patches as nesting sites for this species, in order to mitigate the severe effects of this despotic edge specialist.     

Genetic structure at three spatial scales is consistent with limited philopatry in Ricord's Rock Iguanas (Cyclura ricordii)

Cyclura ricordii is an endemic iguana from Hispaniola Island and is threatened on the IUCN Red List. The main threats are predation by introduced mammals, habitat destruction, and hunting pressure. The present study focused on two nesting sites from Pedernales Province in the Dominican Republic. The hypothesis that natal philopatry influences dispersal and nest‐site selection was tested. Monitoring and sampling took place in 2012 and 2013. Polymorphic markers were used to evaluate whether natal philopatry limits dispersal at multiple spatial scales. Ripley's K revealed that nests were significantly clustered at multiple scales, when both nesting sites were considered and within each nesting site. This suggests a patchy, nonrandom distribution of nests within nest sites. Hierarchical AMOVA revealed that nest‐site aggregations did not explain a significant portion of genetic variation within nesting sites. However, a small but positive correlation between geographic and genetic distance was detected using a Mantel's test. Hence, the relationship between geographic distance and genetic distance among hatchlings within nest sites, while detectable, was not strong enough to have a marked effect on fine‐scale genetic structure. Spatial and genetic data combined determined that the nesting sites included nesting females from multiple locations, and the hypothesis of “natal philopatry” was not supported because females nesting in the same cluster were no more closely related to each other than to other females from the same nesting site. These findings imply that nesting aggregations are more likely associated with cryptic habitat variables contributing to optimal nesting conditions.     

Issue Information

The population of Yellow‐naped Amazons (Amazona auropalliata) declined by an estimated 50% between 1980 and 2000, and the current population is estimated to be between 10,000 and 50,000. Poaching of young has been a persistent problem, but the species is also threatened by habitat loss and degradation. Because most aspects of their life history, behavior, and ecology have not been examined in wild populations, we studied Yellow‐naped Amazons with the following objectives: (1) identify the species of trees used for nesting, (2) determine the size and potential function of breeding territories, (3) determine nesting success, and (4) examine their duetting behavior. We located nests at 16 sites on the Pacific Slope of Costa Rica from 1999 to 2008. We searched for nests from January to May. Every nest was visited at least once and some nests were visited every 2–3 weeks throughout the breeding season. We also collected territory and duetting data at one site (Ahogados). The breeding season of Yellow‐naped Amazons was during the dry season (January–May). Yellow‐naped Amazons nested in 21 species of trees, but 68% of nests were located in only five species, and cavities in dead coyols (Acrocomia aculeata) were used most often. We found no association between breeding success and the species of tree in which birds nested. Mean territory size was 25,578 m², and these small areas generally consisted of several trees surrounding a nest tree. Pairs continued to duet throughout the breeding season, suggesting that duetting is important for territory defense. The nest failure rate in our study was 89%, and most nest failures (64%) were due to poaching for the pet trade. We recommend immediate population management and conservation actions, including increased law enforcement to reduce nest poaching, protection of key nesting areas, educational programs, and habitat conservation.     

Nest groups of wild bonobos at Wamba: selection of vegetation and tree species and relationships between nest group size and party size

We examined the location of nest groups, spatial distribution of nests within a nest group, and attributes of individual nests of wild bonobos at Wamba, Democratic Republic of Congo. We also examined the seasonal factors influencing nesting behavior and compared the nest group size with the 1 hr party size during daytime. We defined a nest group to be a cluster of nests that were built in the same evening and found within 30 m from the other nearest nest. Examination of the largest gap within a nest group suggested that 30 m was an acceptable cutoff value. Monthly rainfall or fruit abundance did not significantly influence the monthly mean nest group size. Nests were built in the swamp forest for as many as 13% observation days, suggesting the need for reevaluation of the use of swamp forest by bonobos. The use of swamp forest was influenced not by seasonal rainfall or fruit abundance, but by the fruiting of specific species. Preferred tree species for building nests accounted for 19.8% of standing trees, which suggested that the selection of sleeping sites was not largely restricted by the distribution of specific species. The mean 1 hr party size was almost identical through the day and was similar to the mean nest group size. Parties of bonobos sometimes split into smaller nest groups, especially when feeding on non‐preferred fruits during fruit scarcity. By contrast, when feeding on preferred fruits while ranging in large parties, they often aggregated to form even larger nest groups. When sleeping in small‐ or middle‐sized nest groups, they tended to aggregate the next morning. These tendencies may reflect the gregarious nature of bonobos who prefer to range or sleep together as far as circumstances allow. Am. J. Primatol. 72:575–586, 2010. © 2010 Wiley‐Liss, Inc.