We report how artificial nests can be utilised at scale in nest site-limited areas of Mongolia to create a managed population of Saker Falcons (Falco cherrug), an “Endangered” species that is harvested for international trade. The provision of 5,000 artificial nests created an average annual saker population of 602 (SE ± 59) breeding pairs, producing an estimated 1,735 (SE ± 272) fledglings per annum over the period 2013–2015. Our regular monitoring enabled us to identify the effects of climate and vegetation on breeding performance. A warm and dry climate prior to breeding was associated with earlier egg-laying dates, while warmer conditions during the breeding season increased fledging success. Greater vegetation biomass in the previous growth season was positively related to breeding density and earlier clutch initiation, which was associated with larger clutch size and larger fledged brood size. Furthermore, using small mammal remains from saker pellets collected at artificial nest sites, we found that higher breeding density, earlier egg laying, larger clutch size, and increased nest survival were associated with areas with a higher proportion of small mammal prey in the diet. Our results provided evidence of the role of temporal and spatial variation in climate and prey availability on breeding performance, demonstrating the requirement for dynamic modelling of variable demographic parameters to be incorporated within an adaptive management framework for the sustainable management of the Saker Falcon.

Nest predators use visual, acoustic and chemical cues to locate nests. In the Neotropics, predation is high being the main cause of nest failure. Despite that, it is still not completely clear what kind of information predators are using to find nests or whether predators respond differently according to habitat characteristics. Here, we executed an experimental manipulation to investigate how different ecological factors influence nest predation probability. We hypothesised that egg conspicuousness, nest clustering and a more open vegetation structure would increase nest predation probability, and that nest predation would be higher during the breeding season of most avian species in the region. We used artificial nests baited with plasticine and quail eggs (Coturnix coturnix), manipulated egg coloration and nest density. Artificial nests were distributed over forest and savanna-like vegetations. Overall predation rate was 40.9%. We found that nests baited with conspicuous eggs, located in open habitats, at higher densities and during the dry period were more predated. Results suggest that main predators must be visually orientated, and that egg crypsis is an important trait for open-nest species in the area. Moreover, a higher nest density may affect predator behaviour, favouring an increase in nest searching, which may be facilitated in open habitats.

Introduced rats depredate every life stage of island nesting seabirds, but the extent of predation is rarely quantified. Introduced black rat (Rattus rattus) and native deer mouse (Peromyscus maniculatus anacapae) predation on Xantus's murrelet (Synthliboramphus hypoleucus scrippsi) nests was experimentally quantified using artificial nests before and after rat eradication on Anacapa Island (California). The staged rat eradication programme provided experimental treatments: in 2002 rats were eradicated on one island (East Anacapa Islet) and remained on two islands (Middle and West Anacapa Islets), providing a control comparison, and, in 2003, rats were eradicated from the remaining islands (Middle and West Anacapa Islets). In 2002, 96% of artificial nests were depredated on control islands (rats present) with rats accounting for most predation. Nest predation on the treatment island (rats eradicated) in 2002 was significantly lower: 8% of artificial nests were depredated, mostly by endemic deer mice. In 2003, following rat eradication on the remaining islands (Middle and West Anacapa Islets), nest predation was reduced from 96% in 2002 to 3% of total nests in 2003. Predation of nests on East Anacapa Islet (rats eradicated in 2002) increased significantly due to reintroduction and recovery of native deer mouse populations, with 23% of artificial nests depredated. The inference is that rat predation on real Xantus's murrelet nests was responsible for the historically low nesting success and small population sizes of breeding murrelets on Anacapa Island. With rats removed, the hatching success of Xantus's murrelet chicks and the number of individuals nesting on Anacapa Island will increase dramatically. Artificial nest studies are particularly well suited to quantifying introduced rat impacts on hole and crevice nesting seabirds and can simultaneously serve as an effective monitoring tool to detect the presence of rats and the recovery of native nest predators.