Nocturnal courtship,copulation, and egg-laying in the western grebe (<Emphasis Type="Italic">Aechmophorus occidentalis</Emphasis>) and Clark’s grebe (<Emphasis Type="Italic">Aechmophorus clarkii</Emphasis>)

Grebes (Podicipedidae) are primarily diurnal although migration occurs at night and some species forage opportunistically at night. We used motion-activated cameras to study nocturnal reproductive activities of the western grebe, Aechmophorus occidentalis, and Clark’s grebe, Aechmophorus clarkii, at Clear Lake, California, USA, during 2014–2016. During 9283 h of monitoring, 19.4% of rushing displays (n = 75) and 8.4% of copulations (n = 435), plus two weed dancing displays and four instances of egg-laying, occurred at night. Nocturnal copulation and egg-laying often occurred on empty, recently abandoned nests, but some incubating pairs of grebes also copulated at night. Nocturnal reproductive activities occurred more frequently at nests attached to submergent vegetation in open water far from shore when water levels were low than on nests attached to emergent vegetation close to shore when water levels were high, probably due to a reduced risk of predation by nocturnal mammals farther from shore. Nocturnal reproductive activities were not in response to elevated light levels at night, daylight disturbances, diurnal predation, high temperatures on hot days, or sexual interference during daylight. Instead, grebes attempted to increase mating investment and minimize parental investment by exploiting recently abandoned nests at night, and perhaps by undertaking extrapair copulations under the cover of darkness, but some pairs of grebes may simply extended routine reproductive activities into the night. Reproductive activities are probably limited at night by the need to feed during daylight and sleep at night, and by the increased risk of predation by mammals at night. Given the high costs of construction and maintenance of floating nests and the obvious benefit of quickly exploiting abandoned nests, nocturnal reproductive activities may occur more frequently in grebes and other waterbirds using floating nests than in other groups of birds whose reproductive activities occur mostly during daylight.     

Foraging behaviour of nest predators at open-cup nests of woodland passerines

Nest predation patterns and processes cannot be understood without studying the behaviour of predators. I videotaped the behaviour of 22 species of predators at 171 depredated nests of 13 passerine species, in woodland in the Czech Republic. About 32% (60/187) of all events occurred during the night; mammals accounted for 95% (57/60) and 22% (28/127) of nocturnal and diurnal predation, respectively. About 67% (57/85) of mammalian predation, but only 3% (3/102) of avian predation, occurred during night. Multiple predations by the same species were detected in at least 7% (6/82) and 42% (37/88) of nests depredated by mammals and birds, respectively. Martens Martes martes/foina took nest content mostly all at once; birds (mainly Jay Garrulus glandarius) revisited partially depredated nest during 1–4 consecutive days. Martens stayed at the depredated nest about five times longer than Jays. Martens spent similar time at nests with eggs and nestling, while Jays stayed about twice longer at nests with eggs. Mammals consumed eggs always at the nest (23/23), but took nestlings away in at least 48% (31/64) cases. Birds took the eggs and nestling away in at least 31% (18/58) and 76% (71/94) cases, respectively. Predator visits to active nests without taking the content, repeated partial predation and revisitation of previously depredated nests suggest an effect of memory on predator’s foraging behaviour.     

Predators at bird nests in a northern hardwood forest in New Hampshire

ABSTRACT.   Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure.     

Increasing nest predation will be insufficient to maintain polar bear body condition in the face of sea ice loss

Climate change can influence interspecific interactions by differentially affecting species‐specific phenology. In seasonal ice environments, there is evidence that polar bear predation of Arctic bird eggs is increasing because of earlier sea ice breakup, which forces polar bears into nearshore terrestrial environments where Arctic birds are nesting. Because polar bears can consume a large number of nests before becoming satiated, and because they can swim between island colonies, they could have dramatic influences on seabird and sea duck reproductive success. However, it is unclear whether nest foraging can provide an energetic benefit to polar bear populations, especially given the capacity of bird populations to redistribute in response to increasing predation pressure. In this study, we develop a spatially explicit agent‐based model of the predator–prey relationship between polar bears and common eiders, a common and culturally important bird species for northern peoples. Our model is composed of two types of agents (polar bear agents and common eider hen agents) whose movements and decision heuristics are based on species‐specific bioenergetic and behavioral ecological principles, and are influenced by historical and extrapolated sea ice conditions. Our model reproduces empirical findings that polar bear predation of bird nests is increasing and predicts an accelerating relationship between advancing ice breakup dates and the number of nests depredated. Despite increases in nest predation, our model predicts that polar bear body condition during the ice‐free period will continue to decline. Finally, our model predicts that common eider nests will become more dispersed and will move closer to the mainland in response to increasing predation, possibly increasing their exposure to land‐based predators and influencing the livelihood of local people that collect eider eggs and down. These results show that predator–prey interactions can have nonlinear responses to changes in climate and provides important predictions of ecological change in Arctic ecosystems.     

Density- and frequency-dependent predation of artificial bird nests

Predators are often expected to vary their relative predation rates according to the frequency of prey types in the environment (frequency-dependent predation). The underlying cause for this must lie in some dependency of absolute predation rates on the density of prey types in the environment (density-dependent predation). However, frequency-dependent predation may either be caused by 'simple' density-dependent predation, in which the absolute predation rate on a given prey type depends purely on the density of that type, or by more complex responses in which absolute rates depend also on the density of other prey types. It is usually difficult to distinguish the underlying cause of frequency-dependent predation, because frequencies tend to change as densities change. Here, we describe the results of an experiment conducted to disentangle these phenomena under two prey richness (low and high) conditions. We used artificial bird nests (placed on shrubs and on saplings) baited with quail eggs placed in natural forests as models of natural bird nests. Our results indicate that both the absolute and relative predation rates on the prey types may vary in complex ways. Predation rates depend on a complex interaction between the prey's own density, other prey density and the diversity of prey in the environment. Neglecting to include, or consider, these complexities into analyses may lead to erroneous conclusions in studies of absolute or relative predation rates.     

Investigating brown rat <Emphasis Type="Italic">Rattus norvegicus</Emphasis> egg predation using experimental nests and camera traps

Introduced rat species have been implicated in the decline and local extirpation of numerous seabird species from islands across the globe, leading to widespread eradications as a conservation tool. However, little conclusive evidence has been established to determine the direct mechanisms in which rat and seabird species interact. This study aimed to quantify rates of egg predation by brown rats Rattus norvegicus using automated trail cameras at seabird nests baited with domestic quail and hen eggs to represent different-sized seabird eggs. The trail cameras were in situ for a total of 915 days during June and July 2011. Evidence for rats visiting the experimental nests was only observed at one location, where 19 visits were recorded, and no evidence of rat predation on hen or quail eggs was observed. Low levels of rat activity were observed during the study; therefore, it is not possible to conclude that rats never predate seabird eggs as predation may be more likely when rat densities are higher and pressure on food resources greater. This study does however highlight that where rats occur at low densities, predation of eggs is unlikely. Measures aimed at maintaining low abundance of rats in and around vulnerable seabird colonies may therefore be useful where complete eradication is not feasible, although potential for predation of chicks should also be considered.     

Using artificial nests to explore predation by introduced predators inhabiting alpine areas in New Zealand

Abstract

Many bird species endemic to alpine New Zealand are now at critically low densities and restricted in range, making predator‐prey research difficult. We used artificial nests in the Borland Valley, Fiordland National Park, to investigate (1) which introduced species is the most frequent nest predator in the two habitats, (2) whether nest survival differs between habitats, and (3) the utility of artificial nests for guiding conservation management. We used different types of artificial nest in 2 different years and undertook a calibration study of the two types. In 2003, survival of artificial nests containing wax eggs and chicken eggs was high in both habitats. In 2004, survival of artificial nests containing plastilina eggs and chicken eggs was low in both habitats, but was higher in alpine grassland compared with beech forest. Stoats and possums were the most frequent predators (36 and 22% respectively of artificial plastilina nests in alpine grassland and high‐altitude beech forest combined); these percentages did not vary significantly between habitats. Given the low density and sparse distribution of vulnerable species in much of New Zealand, data from artificial nests can be a useful tool for studying predation in these remote and difficult habitats, or at least, preferable to ignorance. However, the type of artificial nest used can strongly affect the rate at which they are destroyed.     

Mesostigmatic mites (Acari: Mesostigmata) in nests of the Eurasian griffon vulture (<Emphasis Type="Italic">Gyps fulvus</Emphasis>) in Croatia

We examined the species composition and community structure of mites of the order Mesostigmata (Acari) in nests of the Eurasian griffon vulture (Gyps fulvus Hablizl, 1783) in Croatia. Material collected from 18 nests included 565 mites belonging to seven species. The most abundant species were Leiodinychus orbicularis (C.L. Koch, 1839) (Trematuridae) and Androlaelaps casalis (Berlese, 1887) (Laelapidae). The results were compared with the community structure and frequency of dominant species of Mesostigmata in nests of 32 other bird species. Leiodinychus orbicularis occurred in the nests of 13 species of birds. It is a typical nidicolous species which occurs most frequently in the perennial nests of birds of prey. In contrast, A. casalis rarely occurs in the nests of birds of prey.     

Meta‐analyses of nest predation in temperate Australian forests and woodlands

Nest predation is the leading cause of nesting failure. Thus it is a crucial area of research needed to inform conservation management and to understand the life history of birds. I surveyed the literature to review the identity of nest predators and the factors affecting nest predation, in Australia using 177 studies. Overall, 94 nest predators were identified when incorporating artificial nests, 69 without. Using only natural nests, the Pied Currawong Strepera graculina was the most frequently reported nest predator. Five nest predators, including Pied Currawong, depredated 40% of the prey measured by the number of prey species taken. Yet, 60% of predation was carried out by the other 64 species, which included by the order of importance birds, mammals, reptiles, frogs and ants. Predation at cup and dome nests was more frequently reported than at burrow, ground and hollow nests. Only 28% of predators were observed at both artificial and natural nests suggesting artificial nests have limited, but not negligible, ability as tools for identifying predators. There was a highly significant and positive correlation between predator and prey masses. The predator prey mass ratio was calculated with a mean 0.25 and a median 0.22, a result closely matching with the proportional size of prey taken by raptors. The finding that predator size is proportional to prey opens a pathway for more life history and conservation research.     

Predation by mustelids and rodents on the eggs and chicks of native and introduced birds in Kowhai Bush, New Zealand

Prior to human settlement the endemic New Zealand avifauna evolved in the absence of mammalian predators. Subsequently mustelids, rodents and feral cats have become established and frequently prey on birds and nests. It has been suggested that, because of their evolutionary history, the endemic birds are especially susceptible to such predators. In this paper predation by mustelids and rodents on the eggs and nestlings of eight species of native bird is compared with that on five species of introduced European passerine inhabiting the same lowland forest.
Final outcomes were known for 101 nests of native birds and 48 nests of introduced birds found during three breeding seasons. There was no significant difference between the two groups in frequency of predation. Native birds lost 70-1% of their nests to predators and introduced birds 64-6%. Most predations occurred during the egg stage. Clutch size did not influence frequency of predation, but brood size did for Fantails and introduced birds. Stoats and weasels were responsible for 77-9% of predations on native birds and 77-4% on introduced birds; corresponding percentages for rodents (principally ship rats) were 14-7% and 19-4%. Mustelids destroyed proportionately more nests with chicks than with eggs, whereas rodents did the reverse. Predation on both groups of birds was not influenced by their nesting habitat, the species of tree used for nesting, or the height and position of the nest. The vulnerability to introduced predators of native New Zealand birds is discussed in relation to the historical declines of many species, and also their life-history patterns.     

Rhodamine-B-marked eggs identify individual predators of artificial nests

Investigations of nest predation are often limited by the researchers’ inability to identify nest predators accurately. I tested a chemical bait marker, Rhodamine B (RB), as an indicator of egg predation at artificial ground nests. In a pen trial, the presence of characteristic fluorescent bands in one or more facial vibrissae from all treatment animals confirmed the suitability of RB as a bait marker in the introduced European hedgehog (Erinaceus europaeus). In a field trial in which artificial ground nests were baited with RB-dosed eggs, five of 21 trapped hedgehogs showed evidence of RB ingestion. One animal showed markings indicating two temporally separate predation events. This ability to identify nest predators to species, demographic class, or individual level could lead to more focused control programmes. Other potential uses of this technique include investigation of individual foraging behaviour, calibration of predation rates in artificial nest studies, estimation of the efficacy of poisoned eggs as a control method, and testing for bait or poison uptake by non-target species.     

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.     

Wait Until Dark? Daily Activity Patterns and Nest Predation by Snakes

Predation involves costs and benefits, so predators should employ tactics that reduce their risk of injury or death and that increase their success at capturing prey. One potential way that predators could decrease risk and increase benefits is by attacking prey at night when risks may be reduced and prey more vulnerable. Because some snakes are facultatively nocturnal and prey on bird nests during the day and night, they are ideal for assessing the costs and benefits of diurnal vs. nocturnal predation. We used automated radiotelemetry and cameras to investigate predation on nesting birds by two species of snakes, one diurnal and the other facultatively nocturnal. We predicted that snakes preying on nests at night should experience less parental nest defence and capture more adults and nestlings. Rat snakes (Pantherophis obsoletus) were relatively inactive at night (23–36% activity) but nearly always preyed on nests after dark (80% of nest predations). Conversely, racers (Coluber constrictor) were exclusively diurnal and preyed on nests during the times of day they were most active. These results are consistent with rat snakes strategically using their capacity for facultative nocturnal activity to prey on nests at night. The likely benefit is reduced nest defence because birds defended their nests less vigourously at night. Consistent with nocturnal predation being safer, rat snake predation events lasted three times longer at night than during the day (26 vs. 8 min). Nocturnal nest predation did not make nests more profitable by increasing the likelihood of capturing adults or removing premature fledging of nestlings. The disconnect between rat snake activity and timing of nest predation seems most consistent with rat snakes locating prey during the day using visual cues but waiting until dark to prey on nests when predation is safer, although designing a direct test of this hypothesis will be challenging.     

Predation of artificial nests by introduced rhesus macaques (<Emphasis Type="Italic">Macaca mulatta</Emphasis>) in Florida,USA

Native throughout Asia, rhesus macaques are believed to have the widest native range of any non-human primate and are capable of adapting to an extensive diversity of habitats. Rhesus macaques have caused environmental degradation in introduced habitats, including decreasing bird populations through nest predation. In the 1930s, rhesus macaques were intentionally introduced into what is today Silver Springs State Park (SSSP), central Florida, in an effort to increase tourism. Our objective was to determine whether introduced rhesus macaques in SSSP would consume eggs presented in artificial nests. We used camera traps adjacent to 100 open-cupped artificial bird nests baited with quail eggs near the Silver River. Nests were placed in shrubs and left in the field site for 12 days, representative of the incubation period of native passerine species. Twenty-one nests were depredated by rhesus macaques, nine by nest predators other than macaques, and five nests by an unidentified predator. Nests were more likely to be depredated by macaques when located in areas of high macaque relative abundance. This study suggests introduced rhesus macaques may influence nest predation rates of native bird species in natural areas.     

Predation risk of artificial ground nests in managed floodplain meadows

Nest predation highly determines the reproductive success in birds. In agricultural grasslands, vegetation characteristics and management practices influences the predation risk of ground breeders. Little is known so far on the predation pressure on non-passerine nests in tall swards. Investigations on the interaction of land use with nesting site conditions and the habitat selection of nest predators are crucial to develop effective conservation measures for grassland birds.In this study, we used artificial nests baited with quail and plasticine eggs to identify potential predators of ground nests in floodplain meadows and related predation risk to vegetation structure and grassland management.Mean daily predation rate was 0.01 (±0.012) after an exposure duration of 21 days. 70% of all observed nest predations were caused by mammals (Red Fox and mustelids) and 17.5% by avian predators (corvids). Nest sites close to the meadow edge and those providing low forb cover were faced with a higher daily predation risk. Predation risk also increased later in the season. Land use in the preceding year had a significant effect on predation risk, showing higher predation rates on unmanaged sites than on mown sites. Unused meadows probably attract mammalian predators, because they provide a high abundance of small rodents and a more favourable vegetation structure for foraging, increasing also the risk of incidental nest predations. Although mowing operation is a major threat to ground-nesting birds, our results suggest that an annual removal of vegetation may reduce predation risk in the subsequent year.     

Identifying predators at nests of small birds in a New Zealand forest

Time-lapse video equipment was used to film continuously at nests of two small passerines, the New Zealand Robin Petroica australis and the Tomtit Petroica macrocephala , in an indigenous broadleaf/hardwood forest in central North Island, New Zealand. The nests were illuminated with infrared light to allow night-time observations of predator and parent bird behaviour, and signs left at nests were linked to predator identity. Introduced Ship Rats Rattus rattus and the small native owl or Ruru Ninox novaeseelandiae were filmed preying on eggs or chicks on 12 occasions, and Ship Rats scavenged on eggs on two occasions. Parent birds sometimes altered the signs left at nests after predation, which confused identification of the predator, while Ship Rat scavenger and predator signs were indistinguishable. This suggests that attempts to identify predators from nest signs could be misleading and potentially a widespread problem. Time-lapse video filming with infrared illumination is potentially the least biased method of identifying predators, but it is expensive and so is best used in conjunction with simpler methods. This study found no evidence that filming altered predation rates or that the predators or parent birds reacted strongly to the camera or lights, so we believe that filming is a valuable and safe technique to guide management for the recovery of critically endangered species that are threatened by predators.     

Functional traits determine heterospecific use of risk‐related social information in forest birds of tropical South‐East Asia

In birds and mammals, mobbing calls constitute an important form of social information that can attract numerous sympatric species to localized mobbing aggregations. While such a response is thought to reduce the future predation risk for responding species, there is surprisingly little empirical evidence to support this hypothesis. One way to test the link between predation risk reduction and mobbing attraction involves testing the relationship between species’ attraction to mobbing calls and the functional traits that define their vulnerability to predation risk. Two important traits known to influence prey vulnerability include relative prey‐to‐predator body size ratio and the overlap in space use between predator and prey; in combination, these measures strongly influence prey accessibility, and therefore their vulnerability, to predators. Here, we combine community surveys with behavioral experiments of a diverse bird assemblage in the lowland rainforest of Sumatra to test whether the functional traits of body mass (representing body size) and foraging height (representing space use) can predict species’ attraction to heterospecific mobbing calls. At four forest sites along a gradient of forest degradation, we characterized the resident bird communities using point count and mist‐netting surveys, and determined the species groups attracted to standardized playbacks of mobbing calls produced by five resident bird species of roughly similar body size and foraging height. We found that (1) a large, diverse subcommunity of bird species was attracted to the mobbing calls and (2) responding species (especially the most vigorous respondents) tended to be (a) small (b) mid‐storey foragers (c) with similar trait values as the species producing the mobbing calls. Our findings from the relatively lesser known bird assemblages of tropical Asia add to the growing evidence for the ubiquity of heterospecific information networks in animal communities, and provide empirical support for the long‐standing hypothesis that predation risk reduction is a major benefit of mobbing information networks.     

Predation on artificial bird nests in chaparral fragments

Summary The predation rate of artificial bird nests was measured in disturbed chaparral habitat fragments and at an unfragmented site in coastal San Diego County, California USA. Local extinctions of chaparral birds has been previously shown to occur in these fragments. The predation rate was highest at the unfragmented site. Among fragments, predation was higher at moderately disturbed than at highly disturbed sites. These results suggest that nest predator species diversity or density is reduced in disturbed chaparral fragments. Nest predation is probably not the most important cause of the observed loss of chaparral breeding bird diversity in these fragments.     

Birds as predators of the pine processionary moth (Lepidoptera: Notodontidae)

The beneficial role of insectivorous birds potentially contributing to the biological control of forest insect pests appears crucial in the context of climate warming, especially for species currently expanding their range such as the pine processionary moth Thaumetopoea pityocampa. Larvae of T. pityocampa are aposematic and carry true urticating setae which, together with overwintering in silk winter nests, prevent them from predation by most insectivorous forest birds. The present review aims at pointing out which bird species can regularly feed on this key forest defoliator throughout its distribution range, and which predation strategies allow birds to cope with the urticating setae carried by late-instar larvae. At least seven bird species can be considered as regular predators of the pine processionary moth: four large migrant specialists (great spotted cuckoo Clamator glandarius, common cuckoo Cuculus canorus, European nightjar Caprimulgus europaeus and Eurasian hoopoe Upupa epops) and three small sedentary generalists (great tit Parus major, crested tit Lophophanes cristatus and coal tit Periparus ater). Each species has developed morphological traits and foraging techniques to feed on different life stages of T. pityocampa throughout the year: (i) gizzard wall structure allowing the consumption of caterpillars with urticating setae (cuckoos); (ii) nocturnal foraging on moth imagos by aerial hawking (nightjars); (iii) ground probing on below-ground pupae with long curved bill (hoopoe); and (iv) shifted predation period in autumn and winter on eggs, early- and late-instar larvae, with particular feeding technique allowing to eat only the inner parts of urticating larvae stages (tits). Although several avian predators regularly feed on T. pityocampa, only a few specialist and generalist insectivorous birds may contribute to regulate its populations, especially when population density of the moth is low. Moreover, their efficiency may possibly be threatened by mismatches associated with climate change.     

Local habitat and landscape influence predation of bird nests on afforested Mediterranean cropland

Afforestation programs such as the one promoted by the EU Common Agrarian Policy have contributed to spread tree plantations on former cropland. Nevertheless these afforestations may cause severe damage to open habitat species, especially birds of high conservation value. We investigated predation of artificial bird nests at young tree plantations and at the open farmland habitat adjacent to the tree plantations in central Spain. Predation rates were very high at both tree plantations (95.6%) and open farmland habitat (94.2%) after two and three week exposure. Plantation edge/area ratio and development of the tree canopy decreased predation rates and plantation area and magpie (Pica pica) abundance increased predation rates within tree plantations, which were also affected by land use types around plantations. The area of nearby tree plantations (positive effect), distance to the tree plantation edge (negative effect), and habitat type (mainly attributable to the location of nests in vineyards) explained predation rates at open farmland habitat. We conclude that predation rates on artificial nests were particularly high and rapid at or nearby large plantations, with high numbers of magpies and low tree development, and located in homogenous landscapes dominated by herbaceous crops and pastures with no remnants of semi-natural woody vegetation. Landscape planning should not favour tree plantations as the ones studied here in Mediterranean agricultural areas that are highly valuable for ground-nesting bird species.