An assessment of tree availability as a possible cause of population declines in scavenging raptors

Lack of suitable nesting trees is an increasingly common issue for avian conservation given rampant habitat and tree destruction around the world. In the African savannah, habitat loss and particularly tree damage caused by elephants have been suggested as possible factors in the decline of large bird species. Given the recent declines of vultures and other scavenging raptors, it is critical to understand if nest availability is a limiting factor for these threatened populations. Loss of woodland, partially due to elephant populations, has been reported for the Mara‐Serengeti ecosystem. Data on characteristics of trees used for nesting were collected for white‐backed, lappet‐faced, white‐headed vulture, and tawny eagle nests in Masai Mara National Reserve, Kenya. Nest tree characteristics were compared with the distribution of a random subsample of trees to assess nest preferences and determine suitability of available trees. Nearest neighbor distances were estimated as well as availability of preferred nesting trees to determine if tree availability is a limiting factor for tree‐nesting vultures. Tree availability was found to greatly exceed nesting needs for African vultures and tawny eagles. We thus conclude that on a landscape scale, tree availability is not a limiting factor for any of the species considered here (white‐backed, lappet‐faced, white‐headed vultures and tawny eagles).     

A description of nesting behaviors,including factors impacting nest site selection,in black‐and‐white ruffed lemurs (Varecia variegata)

Nest site selection is at once fundamental to reproduction and a poorly understood component of many organisms’ reproductive investment. This study investigates the nesting behaviors of black‐and‐white ruffed lemurs, Varecia variegata, a litter‐bearing primate from the southeastern rainforests of Madagascar. Using a combination of behavioral, geospatial, and demographic data, I test the hypotheses that environmental and social cues influence nest site selection and that these decisions ultimately impact maternal reproductive success. Gestating females built multiple large nests throughout their territories. Of these, females used only a fraction of the originally constructed nests, as well as several parking locations as infants aged. Nest construction was best predicted by environmental cues, including the size of the nesting tree and density of feeding trees within a 75 m radius of the nest, whereas nest use depended largely on the size and average distance to feeding trees within that same area. Microhabitat characteristics were unrelated to whether females built or used nests. Although unrelated to nest site selection, social cues, specifically the average distance to conspecifics’ nest and park sites, were related to maternal reproductive success; mothers whose litters were parked in closer proximity to others’ nests experienced higher infant survival than those whose nests were more isolated. This is likely because nesting proximity facilitated communal crèche use by neighboring females. Together, these results suggest a complex pattern of nesting behaviors that involves females strategically building nests in areas with high potential resource abundance, using nests in areas according to their realized productivity, and communally rearing infants within a network of nests distributed throughout the larger communal territory.     

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.     

Use of mistletoes by the Grey Go‐away‐bird (Corythaixoides concolor,Musophagidae) in a semi‐arid savannah,south‐west Zimbabwe

Mistletoes are preferred nesting sites for many bird species in a range of habitats. However, no studies have examined the use of mistletoes by nesting birds in the semi‐arid savannah. We studied nesting in mistletoe and its role in determining nesting success in the Grey Go‐away‐bird in south‐west Zimbabwe. We modelled the effects of mistletoe, mistletoe abundance, nest microclimate, concealment and nest height on daily survival rates (DSR) using program MARK. A constant survival model was best fitted for the Grey Go‐away‐bird suggesting a constant nest survival rate across the nesting period. Mistletoe nests had lower DSR than nests placed elsewhere in the canopy. Mistletoe abundance and nest height had a positive association with DSR whereas visibility distance, microclimate and concealment were negatively associated with DSR. Overall, survival for nests in mistletoe was 22.1% compared with 90.5% for nests in other substrates over the 50‐day nesting period. In conclusion, the low nest survival in mistletoe suggests either that the factors used to select mistletoe as nest sites by these birds are poor predictors of nest success or that nesting in mistletoe may be maladaptive.     

Do trade‐offs between predation pressures on females versus nests drive nest‐site choice in painted turtles?

Predation strongly influences reproductive behaviours because reproducing individuals must balance mortality risks to themselves and to their offspring. In many freshwater turtles, the nest predation risk decreases with nest distance from water, whereas the predation risk to females increases farther from water. To determine whether predation pressure influences the distance from water at which female turtles nest, we measured predation pressure on nesting females and on nests, as well as the distances of nests to water, in two populations of painted turtles. Using models, we found that female survival in both populations was high and did not vary with distance from water. Nest survival was also uncorrelated with nest distance to water, although it was significantly lower than adult survival in both populations and was only 1.2% in one population. Our results suggest that nest sites are not predictably safe from predators. Instead, turtles may hedge their bets by nesting over a wide range of distances from water because any distance is risky for nests and no distance is particularly risky for the nesting female. We suggest that other factors, such as suitable incubation conditions and/or post‐emergence hatchling survival, probably play a larger role than predation in driving nest‐site choice in painted turtles.     

Nest‐site selection and productivity of Vesper Sparrows breeding in grazed habitats

ABSTRACT Livestock grazing in the shortgrass steppe of the Intermountain region of British Columbia may have a negative impact on ground‐nesting birds, but evidence of such an impact is lacking. We examined nest‐site selection and productivity of ground‐nesting Vesper Sparrows (Pooecetes gramineus) across sites with different grazing histories. From 2006 to 2008, we monitored Vesper Sparrow nests and measured vegetation characteristics known to be affected by grazing within nest patches. We used an information‐theoretic approach to test the relative importance of grazing‐affected vegetation variables as predictors of nest‐site selection, nest survival, and nestling condition. Vesper Sparrows selected nest sites with greater cover of late‐seral grass species that decrease in occurrence in response to grazing (i.e., “decreasers”) than was available in random patches in the same territories. Daily nest survival was also lower for nests surrounded by shorter vegetation (odds ratio = 1.12). However, “decreaser” cover was not associated with either of the two indices of productivity measured (daily nest survival probability and nestling condition). In addition, vegetation height, although an important driver of success, was not linked with nest‐site selection, and no vegetation‐cover variable was positively associated with productivity, despite nest concealment being central to our predictions. This suggests that predation risk for nests in areas with shorter vegetation was being elevated through some factor unrelated to concealment. Our results show that grazing reduced both the availability of suitable habitat for and nesting success of Vesper Sparrows, indicating that grazing could pose a threat to population persistence at a broader scale and could potentially contribute to observed declines. Additional research is needed to determine if grazing guidelines in the Intermountain region of British Columbia should be amended, better enforced, or both to prevent regional declines in populations of ground‐nesting grassland birds.     

Absence from the nest due to human disturbance induces higher nest predation risk than natural recesses in Common Eiders Somateria mollissima

Human disturbance of nesting birds may cause reduced breeding success. It is therefore necessary to assess the impact of disturbance to identify steps that minimize negative impacts. We carried out a study of nesting success at two adjacent colonies of Common Eider Somateria mollissima on the islands of Grindøya and Håkøya in northern Norway between 2006 and 2011. Over the study period, nesting success was consistently higher on Håkøya (69–82%) than on Grindøya (35–60%). Between 2009 and 2011 we used camera monitoring of individual nests to identify determinants of nest survival and predation, focusing in particular on the effect of departures from the nest due to human disturbance, which differed between the colonies due to a long‐term research project on Grindøya. Overall, absence of Common Eiders from nests due to disturbance increased the predation risk by a factor of 6.42 for an increase of one additional daily disturbance. In contrast, absence due to natural recesses did not increase nest losses. Under high levels of human disturbance, camera monitoring indicated that the main cause of breeding failure was predation, primarily by Hooded Crows Corvus cornix, but also to some extent Great Black‐backed Gulls Larus marinus. The presence of cameras did not increase the predation risk. Both the presence of researchers and the sight of Common Eider females conspicuously departing from nests are likely to have provided cues to these predators. We suggest management trials to reduce nesting disturbance through the guarding of unoccupied nests to mitigate the effects of human disturbance on reproductive success.     

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.     

Factors Affecting Nesting Site Choice in Chimpanzees at Tshibati,Kahuzi-Biega National Park: Influence of Sympatric Gorillas

We recorded 310 fresh chimpanzee night nests at 72 nest sites to determine their choice of tree and site for nesting vis-à-vis the effects of sympatric gorillas. Chimpanzees did not use trees for nesting according to their abundance, but instead tended to nest in fruit trees that they used as food sources. Nesting patterns of chimpanzees may vary with nesting group size, the type of vegetation, and fruit species eaten or not eaten by gorillas. When chimpanzees lodged as a small group in the secondary forest, they nested more frequently in trees bearing ripe fruits eaten only by themselves than in those with fruit eaten also by gorillas. When they lodged as a large group in the primary forest, they nested more frequently in trees bearing ripe fruits eaten by both apes. Nest group size is positively correlated with the availability of preferred ripe fruits in secondary forest. These findings not only reflect the larger foraging groups at the larger fruiting trees but also suggest that chimpanzees may have tended to occupy fruiting trees effectively by nesting in them and by forming large nest groups when the fruits attracted gorillas. Competition over fruits between gorillas and chimpanzees, due to their low productivity in the montane forest of Kahuzi, may have promoted the chimpanzee tactics.     

A canopy dominant ant affects twig‐nesting ant assembly in coffee agroecosystems

One commonly studied driver of community assembly is the effect of dominant species on subordinate species. Dominant species may impact community assembly during competitive sorting, or recruitment. For ants, important and abundant species in the tropics, several factors may drive community assembly including competition, dispersal, priority effects, and environmental conditions. Although competition is a hallmark of ant ecology, few have examined the influence of patchily distributed dominant ants on other ant species and diversity, especially at the recruitment stage. Here, I consider the impacts of a canopy dominant ant species, Azteca instabilis, and changes in vegetation on twig‐nesting ant colony founding and ant community assembly in a coffee agroecosystem. I added artificial nests to coffee plants in areas with and without A. instabilis four times over a year, and then examined the occupation rate and identity of species colonizing nests. I also examined vegetation characteristics of sites where nests were added. The presence of A. instabilis on coffee plants drastically lowered colonization rates, but nest occupation increased with tree density, and with decreasing proportion of Inga spp. trees in the canopy. The presence of A. instabilis limited the number of nests occupied by six of the ten most common species; most rare species, however, were not affected by A. instabilis presence. Richness of colonizing ants in areas with A. instabilis was lower, but these effects did not significantly affect richness across broader scales. Despite large effects on individual species, species composition did not differ greatly in areas with and without A. instabilis, but some vegetation characteristics (basal area and tree richness) were predictive of ant composition. These results suggest that A. instabilis strongly affects founding events especially for common twig‐nesting species and that both vegetation and influences from this dominant species affect community assembly of twig‐nesting ants at the local scale.     

PVC nest boxes are less at risk of occupancy by feral honey bees than timber nest boxes and natural hollows

Feral European Honey Bee (Apis mellifera) has been identified as a potential nest competitor for Australian hollow nesting species, but few studies have investigated the impact of feral honey bee competition on Threatened species. Our study used data from Glossy Black‐cockatoo (Calyptorhynchus lathami halmaturinus) nests on Kangaroo Island, monitored and managed over an 11‐year period, and found 12% of nests became occupied by feral honey bees during that period. Our results indicate that feral honey bees were less likely to occupy nest boxes made of PVC (5%) compared with wooden nest boxes (24%) or natural hollows in Eucalyptus trees (14%). The removal of feral honey bee hives from nests is a priority for long‐term conservation of glossy black‐cockatoos on Kangaroo Island. We recommend that PVC nest boxes are chosen for future nesting habitat restoration, due to the more frequent use of wooden nest boxes by feral honey bees.     

Nest-Building by Chimpanzees (Pan troglodytes verus) at Seringbara, Nimba Mountains: Antipredation, Thermoregulation, and Antivector Hypotheses

The construction of nests (or beds) for sleeping is a chimpanzee universal, yet little is known about the adaptive function of nest-building. We present an in-depth study of nest-building by unhabituated chimpanzees at the Seringbara study site in the Nimba Mountains, Guinea, West Africa. We recorded 1520 chimpanzee nests over 28 mo during three study periods between 2003 and 2008. We investigated where chimpanzees built their nests, both across the home range and in nest trees, and assessed how altitude and habitat type affected nest site selectivity. We examined whether or not chimpanzees were selective in nest tree choice regarding physical tree characteristics and tree species and assessed plant species preference for both tree- and ground-nesting. We tested three, nonmutually exclusive, hypotheses for the function of arboreal nest-building. We assessed whether selectivity for nest tree characteristics reflected an antipredator strategy, examined whether nesting patterns (both arboreal and terrestrial) and nesting height were influenced by variation in climatic conditions (temperature, humidity, wind), and measured mosquito densities at ground level and in trees at 10 m and related mosquito densities to nesting patterns. Chimpanzees preferred to nest above 1000 m and nested mainly in primary forest. They preferred relatively large trees with a low first branch, dense canopy, and small leaves and showed preference for particular tree species, which was stable across years, whereas plant choice for ground-nesting was largely based on plant availability. We found no support for the antipredation hypothesis, nor did mosquito densities explain arboreal nest-building. The thermoregulation hypothesis was supported, as both nesting patterns and nest-height variation across seasons reflected a humidity-avoidance strategy. Chimpanzees nested higher in trees and at higher altitudes in the wet season. In sum, chimpanzees were selective in their choice of nest sites, locations, and materials, and tree-nesting patterns at Seringbara were best explained by a thermoregulation strategy of humidity avoidance.     

Adaptive latitudinal variation in Common Blackbird Turdus merula nest characteristics

Nest construction is taxonomically widespread, yet our understanding of adaptive intraspecific variation in nest design remains poor. Nest characteristics are expected to vary adaptively in response to predictable variation in spring temperatures over large spatial scales, yet such variation in nest design remains largely overlooked, particularly amongst open‐cup‐nesting birds. Here, we systematically examined the effects of latitudinal variation in spring temperatures and precipitation on the morphology, volume, composition, and insulatory properties of open‐cup‐nesting Common Blackbirds’ Turdus merula nests to test the hypothesis that birds living in cooler environments at more northerly latitudes would build better insulated nests than conspecifics living in warmer environments at more southerly latitudes. As spring temperatures increased with decreasing latitude, the external diameter of nests decreased. However, as nest wall thickness also decreased, there was no variation in the diameter of the internal nest cups. Only the mass of dry grasses within nests decreased with warmer temperatures at lower latitudes. The insulatory properties of nests declined with warmer temperatures at lower latitudes and nests containing greater amounts of dry grasses had higher insulatory properties. The insulatory properties of nests decreased with warmer temperatures at lower latitudes, via changes in morphology (wall thickness) and composition (dry grasses). Meanwhile, spring precipitation did not vary with latitude, and none of the nest characteristics varied with spring precipitation. This suggests that Common Blackbirds nesting at higher latitudes were building nests with thicker walls in order to counteract the cooler temperatures. We have provided evidence that the nest construction behavior of open‐cup‐nesting birds systematically varies in response to large‐scale spatial variation in spring temperatures.     

Raptors breeding on weaver nests in trees and on man-made structures

Several raptor species nest on top of large weaver nests. These weaver nests are usually sited in trees, but 11.7% of Red-billed Buffalo-Weaver Bubalornis niger and 25.7% of Sociable Weaver Philetairus socius nests occur on man-made structures. In an extensive literature search, a total of 16 raptor species were recorded as nesting on top of weaver nests. At least 10 raptor species used weaver nests built in trees. Seven raptor species used weaver nests on man-made sites and four raptor species only used weaver nests built on man-made sites. No owls have been recorded as using weaver nests on man-made sites. There are historical records of raptors nesting on top of weaver nests in trees, while nesting on top of weaver nests sited on man-made structures appears to be a more recent adaptation. Costs and benefits of nesting on man-made sites are briefly listed. Nesting on man-made sites may increase (by both weavers and raptors) and raptor researchers are encouraged to document cases of raptors nesting on weaver nests where these are placed in trees or artificial sites, so that there is a record of changes in frequency of nest site usage by raptors.     

Sleeping tree choice by Bwindi chimpanzees

Unlike nearly all other nonhuman primates, great apes build sleeping nests. In Bwindi Impenetrable National Park, Uganda, chimpanzees build nests nightly and also build day nests. We investigated patterns of nest tree use by Bwindi chimpanzees to understand ecological influences on nest tree selection. We analyzed data on 3,414 chimpanzee nests located from 2000 to 2004. Chimpanzees at Bwindi were selective in their use of nest trees. Of at least 163 tree species known to occur in Bwindi [Butynski, Ecological survey of the Impenetrable (Bwindi) Forest, Uganda, and recommendations for its conservation and management. Report to the Government of Uganda, 1984], chimpanzees utilized only 38 species for nesting. Of these, four tree species (Cassipourea sp., Chrysophyllum gorungosanum, Drypetes gerrardii, and Teclea nobilis) accounted for 72.1% of all nest trees. There was considerable variation in nesting frequencies among the top four species between and within years. However, these species were used significantly more often for nesting than other species in 70.9% (39 of 55) of the months of this study. A Spearman rank correlation found no significant relationship between tree abundance and tree species preference. Ninety-three percent of all nests were constructed in food tree species, although not necessarily at the same time the trees bore food items used by chimpanzees. The results indicate that nesting tree species preferences exist. Bwindi chimpanzees' choice of nesting tree species does not appear to be dependent on tree species density or use of the tree for food. We discuss possible reasons for the selectivity in nest trees by the Bwindi population.     

Nesting ecology of solitary‐nesting Amur Falcons (Falco amurensis) in central Mongolia

Amur Falcons (Falco amurensis) are a migratory species that face a variety of threats across their range, but little is known about their breeding ecology. These falcons breed in forest habitats in Eastern and Central Asia using nests constructed by corvids, including Eurasian Magpies (Pica pica). We monitored nests of 21 pairs of Amur Falcons at Hustai National Park in central Mongolia in 2017. Our objectives were to describe their basic nesting ecology, estimate nest survival by modeling the daily survival rate (DSR), examine nest selection by modeling it as a function of nest and site covariates, and use a spatial simulation to test hypotheses concerning intra‐ and interspecific avoidance. Clutch sizes averaged 4.1 eggs (N = 21 nests), and incubation and nestling periods averaged 25.7 and 26.1 d, respectively. The daily survival rate was 0.98, with young in 12 nests surviving to fledging. Nest structures were more likely to be selected as percent cover of nest bowls increased, usually in the form of a dome of sticks with multiple side entrances. Closed nests likely provide increased protection from predators. In contrast to congeneric Red‐footed Falcons (F. vespertinus) that nest in large colonies, Amur Falcons nested no farther from or closer to nests of either conspecifics or congeners than expected by chance. One factor likely contributing to this difference is that Red‐footed Falcons often use the nests of colonial‐nesting Rooks (Corvus frugilegus), whereas Amur Falcons typically use the nests of non‐colonial Eurasian Magpies. The ongoing loss of deciduous trees like white birch (Betula platyphylla) across the breeding range of Amur Falcons, probably due to climate change and increased grazing pressure, is likely to reduce the availability of nesting habitat for Eurasian Magpies which, in turn, will likely reduce availability of nests for Amur Falcons and other small falcons.     

The impact of elephants on the marula tree Sclerocarya birrea

This study determined the abundance, density and population structure of the marula tree, Sclerocarya birrea, in three game reserves in South Africa, and assessed patterns and amounts of new and cumulative impact of elephants. Elephant feeding was very patchy so several attributes of individual trees, sampled transects and communities that might influence elephant herbivory were investigated. The incidence and type of elephant impact (bark, branch or stem breakage) were significantly related to tree diameter, but not to fruiting nor proximity to roads. At the transect level, elephant impact was influenced by density of marula trees, but was not influenced by proximity to roads, nor proportion of marula trees bearing fruits in the vicinity. At the community level, elephant impact was higher on reserves with higher total marula densities. Fourfold differences in elephant densities (0.08–0.30 elephants km^?2) did not explain marula consumption: the percentage of trees with branch damage was similar across reserves and bark damage was inversely proportional to elephant density. Variation across reserves may reflect local and landscape‐level marula tree abundance, differences in alternative food plants and individual feeding habits. The recorded levels of impact appeared to be sustainable because mortality rates were low, affected trees often recovered, and small trees were not preferentially preyed upon.     

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.     

Enriching small trees with artificial nest boxes cannot mimic the value of large trees for hollow‐nesting birds

Large trees support unique habitat structures (e.g. hollows) that form over centuries and cannot be provided by small trees. Large trees are also declining in human‐modified landscapes worldwide. One restoration strategy gaining popularity involves adding nest boxes to smaller trees to replicate natural hollows. However, limited empirical research has tested how hollow‐nesting fauna responds to the presence of nest boxes. We asked: can the addition of nest boxes increase tree visitation by hollow‐nesting birds? We conducted a before‐after control‐impact (BACI) experiment using 144 nest boxes and 96 sample trees comprised of three sizes (small [20–50 cm dbh], medium [51–80 cm], and large [>80 cm]) and located in four landscape contexts (reserves, pasture, urban parklands, and urban built‐up areas). We recorded a significant increase in hollow‐nesting bird abundance and richness at large trees after nest box additions. However, the same response was not observed at medium, small, or control trees. We also recorded nonsignificant increases in hollow‐nesting bird abundance and richness at trees in modified landscapes after nest box additions compared to trees in reserves and control trees. Our results suggest that adding nest boxes to smaller‐sized trees may not attract hollow‐nesting birds. Therefore, nest box management strategies may require re‐evaluation as it is often assumed that hollow supplementation will attract hollow‐using fauna and sufficiently ameliorate the loss of large, hollow‐bearing trees. We advocate that large tree retention remains crucial and should be prioritized. Large trees could be effective target structures for habitat restoration, especially in modified landscapes.     

Influence of stochastic processes and catastrophic events on the reproductive dynamics of the endangered Maroon‐fronted Parrot Rhynchopsitta terrisi

Stochastic and catastrophic events may strongly impact the dynamics of wild populations. Annual fluctuations in rainfall may affect parrot populations, but few studies address the impact of other stochastic or catastrophic events on their population dynamics. The Maroon‐fronted Parrot Rhynchopsitta terrisi is an endangered species that nests colonially in cavities and crevices in limestone cliffs. From 1995 to 2010, we quantified Parrot attendance at nesting colonies throughout its breeding range, and reproductive output of nesting Parrots from 1997 to 2010 at the two most important nesting colonies. There was significant variation among colonies in the number of cavities occupied by Parrots each year. Rainfall significantly influenced both the number of occupied cavities and productivity, which declined after very dry years. Natural unpredictable events such as hurricanes did not modify the nesting activity of Maroon‐fronted Parrots at breeding colonies. However, wildfires increased in dry years, negatively affecting attendance at breeding colonies. The Maroon‐fronted Parrot may overcome the impacts of climatic variability, natural stochastic processes, and human‐induced catastrophic events by using nesting colonies as a network of resources throughout the breeding range. Given the current trends in climate change, it is likely the species may suffer stronger and more frequent unpredictable catastrophic events, potentially putting at risk its survival in the long term.