Seasonal variation in grey crowned crane (Balearica regulorum) abundance in the Ngorongoro Crater,Tanzania

There are few quantitative estimates of numbers of Africa's endangered grey crowned cranes (Balearica regulorum), yet conservation of this species will depend on such estimates. We used line-transect distance sampling on multiple 2-km segments of an existing road network to estimate the abundance of grey crowned cranes in a portion of the Ngorongoro Crater, Tanzania, during the wet (April) and dry (August) seasons of 2016. We analysed data from 106 transects on which we observed 174 groups of 1–61 cranes (median and mode = 2). Abundance and density estimates on the areas surveyed were best modelled without group size as a covariate and indicated that mean crane densities were significantly lower in the wet season (2.4/km²) than in the dry season (20.2 cranes/km²). Even based on survey areas of different size, minimum estimated numbers of cranes in the Crater (wet season: 108–133; dry season: 362–401) likely reflect the concentration of cranes in the nonbreeding (dry) season in the perennial wetlands of the Crater and reinforce the notion of the Crater being a key seasonal habitat for crane populations in northern Tanzania, as previously suggested in the literature.     

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.     

The Influence of Habitat,Season, and Detectability on Abundance Estimates across an Amazonian Parrot Assemblage

The Amazon basin holds very high parrot species richness but almost nothing is known of parrot population densities in the region or how these vary between species, habitats, sites, and seasons. Such data are becoming important as humans impact on increasing areas of the region. Seventeen parrot species were surveyed using a line transect distance sampling method over 3 yr in floodplain and terra firme forests at two sites in the Tambopata region of southeast Peru. Density estimates for most species were in the range of 3.3–7.8/km², with Brotogeris cyanoptera and Amazona farinosa reaching densities of 22 and 23/km² in floodplain forest during the dry season. Parrot densities were higher in floodplain forest than in terra firme forest at both sites. The parrot communities of terra firme forests were similar across sites and seasons, but those in floodplain forests differed widely across sites and across seasons. Upper canopy birds are notoriously difficult to survey. We introduce a procedure to correct for the likely violation of the assumption that all birds on the transect line are detected (distance sampling assumption g(0) = 1). We correct g(0) based on calling rates of birds using a cue‐counting technique. Multipliers for g(0) differ across species and site, but not season. This method yielded density estimates on average 22 percent higher (6–40% higher in individual species) than those from the standard method.     

Abundance and abundance change in the world's parrots

Estimates of population density and abundance change (differences in density or encounter rates across land uses or time periods) form the cornerstone of much of our knowledge of species' responses to environmental conditions, extinction risks and potential conservation actions. Gathering baseline data on abundance of the world's c. 10 000 bird species and monitoring trends in the light of rapidly changing environmental and harvest pressures is a daunting prospect. With this in mind, we review literature on population densities and abundance changes across habitats in one of the world's largest and most threatened bird families, the parrots (Psittaciformes), to identify gaps in knowledge, model phylogenetic and other influences on abundance, and seek patterns that might guide thinking for data‐deficient taxa and situations. Density estimates were found for only 25% of 356 parrot species. Abundance change data were similarly limited and most came from logged forest, with very few comparisons across different anthropogenic habitats. Threatened species were no more likely to have a density estimate than non‐threatened species, and were less likely to have estimates of abundance change. Exploratory generalized linear mixed models indicated that densities are most influenced by genus, and are generally higher within protected areas than outside. It is unclear whether the latter effect stems from habitat protection, a reduction in poaching or both, but protected areas appear to be beneficial for parrots. Individual members of the ‘parakeet’ genera (e.g. Pyrrhura and Eos) were predictably abundant, whereas within larger‐bodied genera such as Ara (macaws), species were predictably uncommon (< 10 individuals per km²) and there was a long tail of extreme rarity. Responses of parrots to habitat change were highly variable, with natural variation in parrot abundance across different primary forests as great as that between primary forest and human‐altered forests. The speed at which environmental change is affecting the world's parrots far outstrips that of our current capacity to track their abundance and we assess the likely scale of data deficiency in this and other bird groups. Developments in survey and analysis methods such as variants of distance sampling and the integration of niche modelling with point density estimation may increase our effectiveness in monitoring parrots and other important and threatened bird groups.     

Occupancy patterns of the introduced,predatory sugar glider in Tasmanian forests

Introduced mammals pose serious threats to native island fauna, and understanding their distribution is fundamental to evaluating their conservation impact. Introduced sugar gliders (Petaurus breviceps) are the main predator of critically endangered swift parrots (Lathamus discolor) on mainland Tasmania. We surveyed sugar glider occurrence over ~800 km² in an important swift parrot breeding area, the Southern Forests. During 4–5 visits per site, we used call broadcast of predatory owls to elicit sugar glider alarm calls and surveyed 100 sites during February/March 2016. Naïve occupancy by sugar gliders was high (0.79), as was detectability (0.52 ± 0.03 SE), resulting in a cumulative detection probability of effectively 1. Occupancy modelling indicated a positive effect of the proportion of mature forest cover on occupancy. The best model, based on AIC scores, included the proportion of mature forest cover within a 500 m radius with constant detectability. Our study revealed surprisingly high rates of occupancy of available forest habitat throughout the heavily logged study area, such that even when mature forest cover was <10%, sugar glider occupancy was >0.5; where forest cover approached 100% (i.e. in the best quality breeding habitat for swift parrots), occupancy by sugar gliders approached 1. Our results reveal that sugar gliders are widespread across the study area which may be indicative of occupancy rates elsewhere in the breeding range of the critically endangered swift parrot. As a result, the risk of predation by sugar gliders for small birds may be widespread across logged Tasmanian forests. Additional work to identify whether population densities of sugar gliders vary with forest cover (and whether this may impact predation likelihood) is critical to understanding the conservation consequences of deforestation in the breeding range of the swift parrot.     

Population status and habitat preference of Soemmerring’s gazelle in Alledeghi Wildlife Reserve,Eastern Ethiopia

This study was undertaken to determine the current population size, structure and habitat preference of Soemmerring's gazelle [Nanger soemmerringii (Cretzschmar 1828)] in the Alledeghi Wildlife Reserve, NE Ethiopia. Animals were counted, both during dry and wet seasons, along 12 line transects each in three habitat types (grassland, tree‐scattered grassland and bushland) in 2015/16. Habitat type had nonsignificant effect on mean population density of Soemmerring's gazelle, but wet season mean density was significantly higher than dry season mean density. Estimated weighted mean (±95% CI) population density of the species in the reserve was 1.90 (±0.17) and 5.99 (±0.370) individuals/km² during the dry and wet seasons, respectively. Total population size of the species in the Alledeghi Wildlife Reserve was estimated at 826 ± 77 and 2,562 ± 158 individuals during the dry and wet seasons, respectively. Over half of the total population of Soemmerring's gazelle was represented by adult females during both seasons. Seasonal habitat preference of Soemmerring's gazelle was statistically significant, with greater preference for grassland habitat during wet season and for bushland habitat during dry season. In conclusion, this study has provided valuable data that will be used as a baseline for future population monitoring.     

Roosting of Yellow-naped Parrots in Costa Rica: estimating the size and recruitment of threatened populations

ABSTRACT.   Many parrot populations are threatened with extinction due to habitat loss and collection for the pet trade. The loss of nest trees and chick poaching can drastically reduce reproductive success. However, due to the long life span of many parrots, populations are unlikely to become extinct rapidly even with complete reproductive failure. For parrots that travel in family groups, rapid estimates of reproductive success can be obtained by recording group sizes in areas where they congregate. We used roost counts over an 18-month period to estimate the size and productivity of a population of Yellow-naped Parrots ( Amazona auropalliata auropalliata ) in Costa Rica. Up to 300 birds were observed flying to roost on offshore islands near Curú National Wildlife Refuge. Roost counts were lowest during the breeding period (December–March), increased after fledging (April–July), and peaked during the late wet season (September–October). Increased food availability on the islands during the breeding season allowed the parrots to become seasonal island residents, and lowered roost counts during that period. We calculated reproductive parameters by assuming that groups of >2 birds were adults traveling with young. The percentage of young in the population was 12.5% and did not differ between years. Studies of group size in birds that form stable family groups, such as psittacines in the genera Amazona and Ara , are an inexpensive way to obtain estimates of the reproductive output of some parrot populations and determine if further study or intensive management are warranted.     

Factors influencing the abundance of parrots and hornbills in pristine and disturbed forests on New Britain, PNG

We estimated densities of parrot and hornbill species in primary and selectively logged forest and forest gardens at two lowland sites on New Britain, PNG. We related differences in abundance to food and nest-site availability in the different habitats and determined whether nest-site availability might limit local breeding populations. Blue-eyed Cockatoo Cacatua ophthalmica and Blyth's Hornbill Rhyticeros plicatus were usually rarer in forest gardens than in primary forest, but both fared well in logged forest. Eclectus Parrot Eclectus roratus was more common in all human-altered forests than in primary forest, and Eastern Black-capped Lory Lorius hypoinochrous was reasonably common throughout but extremely abundant in forest gardens at one site. Parrots and hornbills were recorded eating fruits of 15 tree species and flowers of nine species. Densities of these fruiting and flowering trees were highest in logged forest and forest gardens, respectively, indicating the importance of these anthropogenic habitats as feeding grounds for the assemblage. Active nest cavities were found in large individuals of 12 tree species. Densities of potential nest cavities were highest in primary forest and lowest in forest gardens. At both sites, estimates of potential nest-site density were significantly lower than estimates of the density of pairs of all species of parrots and hornbills: there may be 10–20 parrot/hornbill individuals per nest-hole. Continuing forest alteration, whilst further reducing nest-site availability, may allow large populations of parrots and hornbills to persist due to increased availability of food in some anthropogenic habitats. However, current abundance of such bird species may be a poor correlate of future extinction risk as long-lived taxa may remain common for some period even when annual recruitment has declined to critically low levels.     

Influence of environmental variability on the growth of Lilac-crowned Parrot nestlings

Growth rate parameters were analysed for Lilac-crowned Parrot Amazona finschi nestlings in the tropical dry forest of the Reserva de la Biosfera Chamela-Cuixmala, Mexico. Growth rates for psittacine species follow the inverse relation with body mass observed for neotropical landbirds, with larger parrot species exhibiting slower growth rates. There was significant variation between years in size and growth rates of Lilac-crowned Parrot nestlings with nestlings exhibiting slower growth rates in 1996 than in 1997. Food abundance for parrots also varied significantly between years, with greater food availability during the 1997 breeding season than that of 1996. The increased size and growth rates of nestlings in 1997 may have reflected this, and suggests the potential influence of environmental variability on parrot reproduction, particularly in such a markedly seasonal habitat.     

Spacing behaviour and habitat use of rock ptarmigan (Lagopus mutus) at low density in the Italian Alps

Studies of rock ptarmigan Lagopus mutus in northern latitudes have shown that, in the breeding season, the majority of cocks pair monogamously and defend small territories, whilst in most populations, a small proportion of cocks are polygynous or remain unmated. Little is known, however, on spacing behaviour and habitat use of alpine rock ptarmigan populations occurring at low densities at the southern edge of the species’ range. From 1995 to 1997, we trapped, radio-tracked and observed birds in the Central Italian Alps (elevation 2,000–3,000 m) in order to investigate spacing behaviour and habitat use in alpine landscapes where habitats offering rich food and cover are patchy. Both sexes were selective in their habitat use, and cocks did not establish territories on bare ground, artificial or nutrient rich grasslands or bogs. In the breeding season, cocks had larger home ranges than hens (cocks 99 ± 57 ha, hens 50 ± 25 ha) that overlapped with the ranges of neighbouring cocks and hens. Cocks were monogamous and defended relatively large territories (core areas of home ranges: cocks 37 ± 26 ha, hens 24 ± 12 ha), which corresponded with low spring densities (0.47–2.29 cocks km⁻² and 0.35–1.60 pairs km⁻²). Territory size of individual cocks was negatively correlated with the amount of high quality habitat in the core-area. Our results suggest increased home ranges and large breeding territories in low density alpine rock ptarmigan populations, compared to populations occurring at higher densities in the central and northern alps, and on subarctic and arctic grounds at northern latitudes, confirming the predictions of models on food-based territoriality.     

Parrot claylick distribution in South America: do patterns of “where” help answer the question “why”?

Geophagy is well known among some Neotropical parrots. The clay apparently adsorbs dietary toxins and/or provides supplemental nutrients. We used location data and 23 environmental layers to develop a predictive model of claylick distribution using Maxent software. We related species characteristics to claylick use and examined how parrot assemblages using claylicks changed with distance from the centre of claylick distribution. Fifty‐two parrot claylicks were reported from an area of ca 4 million km² but over 50% were restricted to a 35 000 km² region of southeast Peru and northern Bolivia. Claylicks were strongly associated with moist forest on younger (<65 millions of yr) geological formations and exposed river banks. The predictive model of claylick distribution matched our reported range well, with precipitation of warmest quarter, land cover, temperature seasonality, and distance from the ocean being most important predictors of claylick presence. Twenty‐six of the region's 46 parrot species visited claylicks. Species differed greatly in their lick use, but body size, dietary breadth, abundance and other traits were poor predictors of lick use. We are confident that our survey identified the distribution of major parrot claylicks in South America, although less conspicuous parrot geophagy may occur elsewhere. We suggest that claylick distribution reflects both underlying geology (allowing claylick formation in only some regions) and the physiological need for geophagy among parrots in different parts of the continent. Data on the latter are inconclusive, but we argue that parrot claylick distribution supports the contention that geophagy is related more to sodium deficiencies than to protection from dietary toxins.     

The ground parrot (Pezoporus wallicus Kerr) in south-eastern Australia: a fire-adapted species?

The ground parrot (Pezoporus wallicus) has a coastal distribution in Victoria and has declined in range since European colonization. Its habitat consists of two major vegetation communities: coastal heathland and sedgeland. These are further divided into various sub-communities. These habitats contained high densities of cyperaceous and restionaceous plants, the seeds of which form the bulk of the bird's diet. Seeds and small fruits of some dicotyledonous plants and grasses are also eaten. Seed production by sedges remains fairly constant over time in sedgelands but varies in heathland, depending on time since burning. This variation is reflected by parallel changes in ground parrot population density. Both long unburnt and very frequently burnt heathlands are unsuitable for ground parrots. The birds also require dense vegetation cover. Ground parrots appear to live in territorial breeding pairs with enforced natal dispersal. This is an adaptation to an environment where habitat is patchily distributed in space and variable in quality over time.     

Ecology of the coprophagous moth Trisyntopa neossophila Edwards (Lepidoptera: Oecophoridae)

Trisyntopa neossophila Edwards (Lepidoptera: Oecophoridae) is an unusual moth whose breeding cycle is closely synchronised with a termite mound nesting parrot of northern Australia; the hooded parrot ( Psephotus dissimilis Collet). T. neossophila is one of three coprophagous, nest dwelling moths in the genus Trisyntopa Lower 1918. True coprophagy is rare in the Lepidoptera, although some species occasionally consume faeces to gain rare nutrients. We present observations of the life cycle of T. neossophila , a moth that lays its eggs in the nest of a hooded parrot, so that larvae hatch in synchrony with the hatching of the parrot's eggs. The larvae spend their larval period in the nest and exclusively consume the excrement of the nestling parrots. When the parrot chicks fledge, the larvae move to the walls of the nest cavity to pupate, emerging the following wet season to repeat the process during the next parrot breeding season.     

Diet and Geophagy Across a Western Amazonian Parrot Assemblage

We identified species‐ and community‐level dietary characteristics for a species‐rich Amazonian parrot assemblage to determine relationships among dietary metrics and use of geophagy sites. Previous studies suggest that soil is consumed at geophagy sites in this region mainly to supplement dietary sodium. We accumulated 1400 feeding records for 16 parrot species over 2 yr and found that seeds, flowers, and fruit pulp featured prominently in diets, while bark, insects, and lichen were consumed in small quantities. Food availability across 1819 trees was measured, and we found that flower availability was highest in the dry season and fruit production peaked in the wet season, but that phenology patterns of the 20 most commonly foraged plant species suggest no serious food bottlenecks. Partitioning of available food resources among the 13 most commonly encountered parrots is suggested by an ordination analysis (DCA), which placed the large macaws (Ara) with the Amazona parrots at the ‘primary forest’ end of a dietary resource axis and four smaller species at the ‘successional forest’ end of the axis. Parrot species associated with successional forest also consumed less plant species overall. Furthermore, these parrot species consuming successional forest resources had higher claylick visitation rates than those consuming primary forest resources suggesting they derive the greatest benefits from soil consumption.     

Intersexual differences in energy expenditure of Anolis carolinensis lizards during breeding and postbreeding seasons

Although the amount of energy that males and females invest in reproduction is an integral component of theories explaining the evolution of particular mating strategies, few studies have actually determined the amount of energy that each sex allocates to reproduction. We compared how energy is expended by male and female Anolis carolinensis lizards during both the breeding and postbreeding seasons. We used laboratory respirometry to determine resting metabolic rates (RMRs) of inactive, freshly captured lizards and the doubly labeled water technique to determine field metabolic rates (FMRs) of free-ranging lizards. Both RMRs and FMRs were influenced by body mass but not by sex. Season did not influence FMRs; however, RMRs of both sexes increased approximately 40% from the breeding to the postbreeding season. The seasonal increase in RMRs was attributed to a postreproductive increase in feeding rate and specific dynamic action. We used RMRs, FMRs, and thermal profiles of lizards to calculate energy budgets for breeding and postbreeding seasons. Energy budgets partitioned daily field energy (DFE; calculated from FMRs) into daily activity energy (DAE) and daily resting energy (DRE; calculated from RMRs). Energy expended for reproduction was estimated as DAE during the breeding season plus egg production (for females). Despite males having 40% greater body mass, females expended 46% more energy for reproduction than did males (906 and 619 J/d, respectively). Total metabolizable energy (TME=DFE+egg production for females) expended during the breeding season was similar for males and females (1,280 and 1,365 J/d, respectively). Although TME of females decreased 44% from the breeding to the postbreeding season (1,365 vs. 766 J/d), TME of males was similar during both seasons (1,280 vs. 1,245 J/d). There were both seasonal and sexual differences in DRE and DAE. Compared with most lizards from semiarid/desert habitats, A. carolinensis in a temperate habitat expends more total energy during the breeding season, allocates more energy to eggs, and appears to have more total energy available for reproduction.     

Moving Window Abundance – A method to characterise the abundance dynamics of farmland birds: The example of Skylark (Alauda arvensis)

Farmland birds are important indicators of the state of biodiversity in rural landscapes, and the occurrence and abundance of birds contribute to their importance as bioindicators. However, the measurement of farmland bird abundance can be difficult. The rapid growth of crop plants in the spring combined with disturbances related to farming practices, such as weed and pest control and other measures, can profoundly change the habitat suitability of arable fields for birds within a short period of time. Consequently, the existing dynamics must be incorporated into the applied methods, and a single value of bird abundance during the breeding season is insufficient to characterise the habitat functions of arable land. The abundance of farmland bird species is influenced by crop specific features, which profoundly change within the breeding season and which we have described using a novel concept called Moving Window Abundance. Based on field surveys in 29 observation areas within arable landscapes, each 1 km², Skylark with territorial behaviour were counted using a mapping method related to the habitats and growth of field crops, such as wheat and maize. To describe the dynamic characteristics of the abundance during the breeding season over the time period from 16 March to 18 July, three methods of Moving Window Abundance were tested: patchy, adjacent and overlapping. These methods differ in the time-space continuity of the considered time window throughout the breeding season. In the Patchy Moving Window Abundance method, we used the exact days in which field surveys were conducted throughout the entire time period of the field surveys. However, with the Adjacent Moving Window Abundance method, the time window included five-day, ten-day and semi-monthly adjacent windows; in the Overlapping Moving Window Abundance method, the time window shifted daily, with five-day, ten-day and semi-monthly overlapping windows used in the calculation procedure. The results indicated that the dynamic nature of Skylark abundance (i) reached a maximum level in the first breeding period in the agricultural landscape and (ii) exhibited large variations in level and time within the various field crops. Therefore, abundance was not described conventionally using a single numerical value but rather using mathematical functions based on the spatial scale of the landscape and habitat. We conclude with recommendations for further research to standardise farmland bird monitoring.     

Seasonal colour change by moult or by the abrasion of feather tips: a comparative study

Many birds undergo seasonal changes in plumage coloration by prebreeding moult, abrasion of cryptic feather tips, or both. Seasonal dichromatism is thought to result from optimizing coloration to the conflicting demands of different life-cycle periods, sexual selection for conspicuousness being substantial during the mating season, whereas selection for camouflage and for social signals may act in all seasons. Furthermore, energetic and time demands may constrain the extent of moult, thereby limiting colour change. We investigated the relative importance of several factors in shaping this variation in a songbird clade using phylogenetic comparative methods. We found that prebreeding moult relates most strongly to breeding onset and winter diet, demonstrating that both time and food availability constrain feather replacement. Feather abrasion was best predicted by winter flocking behaviour, and secondarily by open habitats, implying that exposure to predators and the simultaneous need for social signalling may favour the expression of partially obscured ornaments in the non-breeding season. The combined occurrence of prebreeding moult and feather abrasion was associated with the polygynous mating system, suggesting that species under strong sexual selection may employ both strategies of colour change to ensure the full expression of breeding coloration.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 711–721.     

Life on the edge: Northern bobwhite ecology at the northern periphery of their range

Over the past 40 years, Northern bobwhite (Colinus virginianus) populations have declined range-wide. The Mid-Atlantic once held the highest densities in the country and now shows some of the worst declines. Although population parameters have been quantified throughout most of the bobwhite range, Mid-Atlantic populations have been largely unstudied. To better quantify the dynamics of this declining system, we sought to not only gather annual data on home range, movement, and habitat selection, but also examine how some of these metrics might impact survival. We captured and radio-tracked 154 bobwhites between May 2006 and April 2008 on a 125 km² area of Cumberland County, New Jersey, USA. Seasonal daily movement ranged from 146 m to 158 m but several extreme movements were notable. Across seasons, grassland habitat was used in greater proportion to its availability, shrub-scrub and agriculture habitats were used equally with their availability and forests and other habitats were used less than their availability. Differences in second-order selection occurred between seasons with lower use of shrub-scrub and forest habitats and higher use of other habitat in breeding seasons. Pooled breeding season survival was 0.343, nonbreeding season survival was 0.183, and annual survival was 0.063. Although mortality was dominated by avian predators, house cat mortalities were noteworthy. Cox proportional hazard analysis revealed that risk of breeding season mortality risk was increased by longer daily movement, lower grassland use, and higher forest and other use. During the nonbreeding season, risk of mortality increased with shorter daily movement and proximity to occupied buildings and barns. This information could inform management decisions in the greater Mid-Atlantic as well as other areas of their range where they exist at very low abundances. © 2010 The Wildlife Society.     

Nest‐site characteristics,breeding success and competitive interactions between two recently sympatric apex predators

An influential period in avian life‐cycles is the annual breeding season, when competition over suitable nesting sites and territories is a key factor that can determine fitness and distribution, especially for species that are highly selective in their nesting habitats. We analysed nest‐site characteristics, breeding success and competitive interactions between two apex predator populations. Whereas the Short‐toed Eagle Circaetus gallicus has nested in the Judean Foothills (Israel) for a long time, the Long‐legged Buzzard Buteo rufinus has only invaded the nesting habitat of the Short‐toed Eagle during their breeding season in the last two decades. These two recently sympatric species have similar nesting ecology and frequently use the same nests. They are therefore expected to compete over nesting sites and territories. We analysed interspecific interactions between these two species by combining information from comprehensive observational, experimental, GIS analysis and remote sensing data, deriving 65 variables to characterize the nest‐sites used and the breeding success in 381 breeding attempts over four consecutive breeding seasons. To assess interspecific and intraspecific territorial behaviour and aggressiveness, stuffed Long‐legged Buzzards and Short‐toed Eagles were presented close to nests. Nest‐site characteristics overlapped substantially between species, and Long‐legged Buzzards occupied 21% of all Short‐toed Eagle nests. Intraspecific aggression rates among Long‐legged Buzzards were higher than their interspecific aggression rates with Short‐toed Eagles and also higher than intraspecific aggression among Short‐toed Eagles. Long‐legged Buzzard and Short‐toed Eagle breeding densities (1.59 ± 0.11 and 2.96 ± 0.11 pairs per 10 km², respectively) are likely to be the highest across their respective breeding distributions, with a maximum productivity of 0.96 ± 0.01 and 0.56 ± 0.05 (young fledged/breeding pair) for Long‐legged Buzzard and Short‐toed Eagle, respectively. Intraspecific interactions among both species play an important role in determining their breeding success and the spatial distribution of nesting sites. Our results suggest that interspecific competition over nesting sites and territories between both species, and the potential dominance of Long‐legged Buzzard, has both direct and indirect impacts on the spatial and demographic distribution of Short‐toed Eagles due to the recent establishment of Long‐legged Buzzard territories in the Judean breeding area.