The use and function of snake skins in the nests of Great Reed Warblers Acrocephalus arundinaceus

We documented and experimentally tested the use of snake skins in construction of nests in a Great Reed Warbler Acrocephalus arundinaceus population in southwestern Slovakia. There was no difference in predation rates of artificial nests that did or did not contain sloughs. We suggest that snake skins in Great Reed Warbler nests may serve as a post‐pairing signal revealing female parental quality.     

Survival of Reed Warbler Acrocephalus scirpaceus clutches in relation to nest position

Nest survival was studied in relation to nest position of 164 nests of the Reed Warbler Acrocephalus scirpaceus in the Southeastern part of the Czech Republic in 1993. Breeding was successful in 91 (55.5%) cases, whereas 40 (24.4%) were predated, 19 (11.6%) were parasitized by the Cuckoo Cuculus canorus and 14 (8.5%) were destroyed by other causes. Of the predated nests, small mammals accounted for 26 (65.0%) and unknown predators for 14 (35.0%) nests. Rates of predation and parasitism varied in relation to a series of habitat factors and Reed Warblers avoided nest sites most vulnerable to predation or parasitism. Concealed places in the vegetation far away from trees were the safest nest sites.     

Common Cuckoo Cuculus canorus and host behaviour at Reed Warbler Acrocephalus scirpaceus nests

This study is based on continuous video recordings made at 53 Reed Warbler Acrocephalus scirpaceus nests each day during the laying period. Egg-laying by the Common Cuckoo Cuculus canorus was recorded in 14 (26.4%) of these nests. By analysing the activity of the host birds around and at the nest, we found that this is probably not the only cue used by the Common Cuckoo when locating suitable nests to parasitize. Furthermore, in most cases there was no significant difference between the length of time the host birds spent at the nest in the morning and afternoon, thus providing little support for the hypothesis that the Common Cuckoo lays in the afternoon because it is less likely to be seen by the nest owners then. Parasitized Reed Warblers rejected the Common Cuckoo egg more frequently when they observed the parasite at their nests. However, contrary to what should be expected, most Common Cuckoos laid their eggs in the presence of the host(s), and in general their egg-laying behaviour (for example duration of stay at the nest) was less secretive than described earlier. When partially depredating host clutches, Cuckoos showed the same behavioural pattern at parasitized and unparasitized nests, indicating that the latter may act as a potential reserve for egg-laying.     

Mortality of Wood Warbler Phylloscopus sibilatrix nests in Welsh Oakwoods: predation rates and the identification of nest predators using miniature nest cameras

Capsule Predation was the main cause of nest failure, but predation rates have remained unchanged since the 1980s. Eurasian Jays Garrullus glandarius were the most common predator.

Aims To quantify, and compare, nest predation rates for 1982–84 and 2009–11, and to identify predators of Wood Warbler Phylloscopus sibilatrix nests in Welsh oakwoods.

Methods During 2009–11, 167 Wood Warbler nests were monitored and purpose-built miniature nest cameras deployed at 73 of them. Nest predation rates were compared with 67 nests monitored during 1982–84.

Results Of 167 nests monitored from 2009 to 2011, 62 failed due to predation (32/73 camera nests, 30/94 non-camera nests), giving an overall Daily Survival Rate (DSR?±?se) of 0.979?±?0.003. This was not significantly different from the rate during 1982–84 (0.967?±?0.006). In 2009–11, the DSR of nests declined temporally during the season at both the egg and chick stages. For chick stage nests, DSR varied annually and nonlinearly with age of nestlings. There was no evidence for an effect of cameras at either stage. Of 32 camera nests lost to predation, the predator was identified from 28, resulting in 30 predators being identified. There was one case of multiple predators at a single nest. The majority of nest predation was carried out by birds (28/30), predominantly Eurasian Jays (18/28), but also Common Buzzards Buteo buteo (5/28), Great Spotted Woodpeckers Dendrocopos major (3/28) and Eurasian Sparrowhawks Accipiter nisus (2/28). There was one predation by both a Eurasian Badger Meles meles and a Red Fox Vulpes vulpes. There were no records of Grey Squirrels Sciurus carolinensis depredating nests.

Conclusions Nest predation rates were similar in both periods, suggesting that increased rates of nest predation have not been driving the decline of the Wood Warbler population in Wales. Deployment of nest cameras did not affect nest survival rates and were successful in identifying nest predators, the majority of which were avian, especially Eurasian Jays. Knowledge of the identity of nest predators can aid the development of conservation measures.     

Common Cuckoos Cuculus canorus change their nest‐searching strategy according to the number of available host nests

In recent decades, numerous studies have examined factors affecting risk of host nest parasitism in well‐known avian host–parasite systems; however, little attention has been paid to the role of host nest availability. In accordance with other studies, we found that nest visibility, reed density and timing of breeding predicted brood parasitism of Great Reed Warblers Acrocephalus arundinaceus by the Common Cuckoo Cuculus canorus. More interestingly, hosts had a greater chance of escaping brood parasitism if nesting was synchronized. Cuckoo nest searching was governed primarily by nest visibility at high host‐nest density. However, even well‐concealed nests were likely to be parasitized during periods when just a few hosts were laying eggs, suggesting that Cuckoos adjust their nest‐searching strategy in relation to the availability of host nests. Our results demonstrate that host vulnerability to brood parasitism varies temporally and that Cuckoo females are able to optimize their nest‐searching strategy. Moreover, our study indicated that Cuckoos always manage to find at least some nests to parasitize. Thus, in this case, the co‐evolutionary arms race should take place mainly in the form of parasitic egg rejection rather than via frontline pre‐parasitism defence.     

Geographic variation in parasitism rates of two sympatric cuckoo hosts in China

Rates of brood parasitism vary extensively among host species and populations of a single host species. In this study, we documented and compared parasitism rates of two sympatric hosts, the Oriental Reed Warbler (Acrocephalus orientalis) and the Reed Parrotbill (Paradoxornis heudei), in three populations in China. We found that the Common Cuckoo (Cuculus canorus) is the only parasite using both the Oriental Reed Warbler and Reed Parrotbill as hosts, with a parasitism rate of 22.4%-34.3% and 0%-4.6%, respectively. The multiple parasitism rates were positively correlated with local parasitism rates across three geographic populations of Oriental Reed Warbler, which implies that higher pressure of parasitism lead to higher multiple parasitism rate. Furthermore, only one phenotype of cuckoo eggs was found in the nests of these two host species. Our results lead to two conclusions: (1) The Oriental Reed Warbler should be considered the major host of Common Cuckoo in our study sites; and (2) obligate parasitism on Oriental Reed Warbler by Common Cuckoo is specialized but flexible to some extent, i.e., using Reed Parrotbill as a secondary host. Further studies focusing on egg recognition and rejection behaviour of these two host species should be conducted to test our predictions.     

Experiments with artificial nests on predation in reed habitats

We performed nest predation experiments with artificial nests in reedbeds investigating whether nest predation pressure is different at the water-reed edge and the grassland-reed edge compared with the reed interior. Furthermore, we tested the effects of vegetation structure (reed density, height and thickness) and the effect of other nest site characteristics (distance from edge, water depth) on the success of artificial nests. The experiments were completed 3 times during the breeding season in 2001 at Lake Neusiedl, Austria. Each artificial nest resembled Great Reed Warbler (Acrocephalus arundinaceus) nests and contained one plasticine and one Quail (Coturnix coturnix) egg and the predators were identified by marks left on the eggs. The potential predators were birds, probably the Marsh Harrier (Circus aeruginosus), gulls (Larus spp.) and reed warblers (Acrocephalus spp.). Nest survival data were analysed using the Mayfield method, and we performed a discriminant analysis for the data of vegetation and nest site characteristics. The nest predation was higher at the edges than in the reed interior, and was most pronounced in April, before the new reed sprouted. The reason for this finding was probably that after May the new reed contributed to greater concealment of the nests through the higher reed density and height.     

Avian brood parasitism in a Mediterranean region: hosts and habitat preferences of Common Cuckoos Cuculus canorus

Capsule Cuckoos in Italy support the ‘host preference’ hypothesis.

Aims To identify the species parasitized in a Mediterranean area, in Italy; to quantify the frequency of parasitism on each host species; and to determine whether some species and/or habitat types are parasitized more than expected from a homogeneous distribution.

Methods Nest records dating from 1865 were compiled from literature, nest card programmes, and personal communication with ornithologists working in the region. Comparisons of parasitism frequencies were made among and within habitats for all cuckoo hosts.

Results The most frequently parasitized hosts were Great Reed Warbler, European Robin, Marsh Warbler, Redstart, and Reed Warbler. The highest number of parasitized species was in anthropic areas (15 host species), whereas wetlands supported the highest number of parasitized nests (471).

Conclusion Cuckoos select a different suite of hosts in Italy from those in continental Europe, but this was not always explained on the basis of different geographical distribution. Results support the ‘host preference’ hypothesis. We suggest further analyses to avoid over‐ or underestimates of parasitism on each host species when parasite preferences are examined.     

人工巢箱条件下的大山雀巢捕食

于2004—2008年在次生阔叶林中,采用悬挂巢箱的方法对大山雀的巢捕食作了研究。结果表明:不同年龄巢箱的被捕食率显著不同,新巢箱被捕食率最低,第2年被捕食率最高,第3年下降很大,第4年又略有上升。被捕食巢的窝卵数极显著的低于未被捕食巢的窝卵数。影响巢捕食的主要生境因子为巢箱高度和巢上盖度,其次为灌木的密度和高度。     

Nest defence,enemy recognition and nest inspection behaviour of experimentally parasitized Reed Warblers Acrocephalus scirpaceus

Capsule Reed Warblers in a regularly parasitized population do not recognize Cuckoo Cuculus canorus as a special enemy and do not change their behaviour at nest immediately after being parasitized.

Aims To assess if an intruder near the nest influences the behaviour of the Cuckoo host.

Methods Host responses to Cuckoo, control Pigeon dummies and human intruder were observed. Host behaviour at 71 nests was video-recorded for 30 minutes at four experimental groups of nests: Cuckoo dummy, Cuckoo dummy + Cuckoo egg, Pigeon dummy, human intruder.

Results Reed Warblers did not respond differently to the Cuckoo and the control species. The experimental procedure had no significant effect on the behaviour of hosts during the study period. We were unable to find any differences in the time spent at the nest, clutch inspection behaviour and nest defence behaviour between morning and afternoon experimental groups. Our results do not support the hypothesis that afternoon laying by the Cuckoo is maintained by a selection pressure from the host. We observed no ejection or egg-pecking during the 30-min period after the experimental parasitism.

Conclusions Low aggression and non-specificity of host responses in our study area are in line with the fact that the Reed Warbler is an intermediate rejecter of Cuckoo eggs as expected from the spatial habitat structure hypothesis.     

Function of egg punctures by Shiny Cowbirds in parasitized and nonparasitized Creamy‐bellied Thrush nests

ABSTRACT Avian brood parasites usually remove or puncture host eggs. Several hypotheses have been proposed to explain the function of these behaviors. Removing or puncturing host eggs may enhance the efficiency of incubation of cowbird eggs (incubation‐efficiency hypothesis) or reduce competition for food between cowbird and host chicks in parasitized nests (competition‐reduction hypothesis) and, in nonparasitized nests, may force hosts to renest and provide cowbirds with new opportunities for parasitism when nests are too advanced to be parasitized (nest‐predation hypothesis). Puncturing eggs may also allow cowbirds to assess the development of host eggs and use this information to decide whether to parasitize a nest (test‐incubation hypothesis). From 1999 to 2002, we tested these hypotheses using a population of Creamy‐bellied Thrushes (Turdus amaurochalinus) in Argentina that was heavily parasitized by Shiny Cowbirds (Molothrus bonariensis). We found that 56 of 94 Creamy‐bellied Thrush nests (60%) found during nest building or egg laying were parasitized by Shiny Cowbirds, and the mean number of cowbird eggs per parasitized nest was 1.6 ± 0.1 (N= 54 nests). At least one thrush egg was punctured in 71% (40/56) of parasitized nests, and 42% (16/38) of nonparasitized nests. We found that cowbird hatching success did not differ among nests where zero, one, or two thrush eggs were punctured and that the proportion of egg punctures associated with parasitism decreased as incubation progressed. Thus, our results do not support the incubation‐efficiency, nest‐predation, or test‐incubation hypotheses. However, the survival of cowbird chicks in our study was negatively associated with the number of thrush chicks. Thus, our results support the competition‐reduction hypothesis, with Shiny Cowbirds reducing competition between their young and host chicks by puncturing host eggs in parasitized nests.     

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.     

Predators of Greater Sage‐Grouse nests identified by video monitoring

ABSTRACT Nest predation is the primary cause of nest failure for Greater Sage‐Grouse (Centrocercus urophasianus), but the identity of their nest predators is often uncertain. Confirming the identity of these predators may be useful in enhancing management strategies designed to increase nest success. From 2002 to 2005, we monitored 87 Greater Sage‐Grouse nests (camera, N= 55; no camera, N= 32) in northeastern Nevada and south‐central Idaho and identified predators at 17 nests, with Common Ravens (Corvus corax) preying on eggs at 10 nests and American badgers (Taxidea taxis) at seven. Rodents were frequently observed at grouse nests, but did not prey on grouse eggs. Because sign left by ravens and badgers was often indistinguishable following nest predation, identifying nest predators based on egg removal, the presence of egg shells, or other sign was not possible. Most predation occurred when females were on nests. Active nest defense by grouse was rare and always unsuccessful. Continuous video monitoring of Sage‐Grouse nests permitted unambiguous identification of nest predators. Additional monitoring studies could help improve our understanding of the causes of Sage‐Grouse nest failure in the face of land‐use changes in the Intermountain West.     

The influence of landscape features on nest predation rates of grassland‐breeding waders

In Europe, lowland wet grasslands have become increasingly fragmented, and populations of waders in these fragments are subject to unsustainably high levels of nest predation. Patches of taller vegetation in these landscapes can support small mammals, which are the main source of prey for many predators. Providing such patches of habitat could potentially reduce levels of nest predation if predators preferentially target small mammals. However, predator attraction to patches of taller vegetation for foraging, shelter, perching and/or nesting could also result in local increases in predation rates, as a consequence of increased predator densities or spill‐over foraging into the surrounding area. Here we assess the influence of taller vegetation on wader nest predation rates, and the feasibility of managing vegetation structure to alter predator impacts. Between 2005 and 2011, the nest distribution and hatching success of Northern Lapwings Vanellus vanellus, which nest in the open, and Common Redshanks Tringa totanus, which conceal their nests in vegetation, were measured on a 487‐ha area of wet grassland in eastern England that is primarily managed for breeding waders. Predation rates of Lapwing nests increased significantly with distance from patches of taller vegetation, and decreased with increasing area of taller vegetation within 1 km of the nest, whereas neither variable influenced Redshank nest predation probability. These findings suggest that the distribution and activity of nest predators in lowland wet grassland landscapes may be influenced by the presence and distribution of areas of taller vegetation. For Lapwings at least, there may therefore be scope for landscape‐scale management of vegetation structure to influence levels of predation in these habitats.     

Breeding ecology of the Eastern Great Reed Warbler Acrocephalus arundinaceus orientalis at Lake Kasumigaura,central Japan

CapsuleTwo populations of the Eastern Great Reed Warblers, one close to settlements and one far away, differed mainly in nest losses which were higher at the latter site.

Aims To compare the breeding ecology of two Japanese populations, and with breeding data from Polish sites.

Methods We studied two sites in 1996. The Seimei site comprises a natural reed-bed (Phragmites australis) (2.0 ha) c. 2 km from residential areas. The Sakura site occurs as smaller reed-bed (0.8 ha) close to residential areas. Field study comprised mainly nest searching and nest monitoring.

Results Breeding density, nest height, number of stems supporting nest, clutch size and brood size were not significantly different between sites. The proportion of nests built on reed stems standing in the water (60%) was significantly higher at the Seimei site (P < 0.001), and the warblers in this habitat experienced significantly higher nesting failure (P < 0.05). Predation was a principal cause of failure at both sites. Significantly more nests suffered from predation at Seimei (53%) than at Sakura (16%). Breeding density was higher at both sites compared with European populations but it fell within ranges of other Japanese populations. Mean first-egg date of first brood does not differ between our sites and Polish ones.

Conclusion The differences between the two Japanese populations and between Japanese and Polish populations were relatively small and were seen mainly in nest losses, breeding density and proportion of nests built over water.     

Different nest predator guild associated with egg size in the Patagonian temperate forest

Capsule: Studies of nest predation using artificial nests need to consider the effect of egg size on the types of predator that are detected.

Aims: To estimate the nest predation rate in the Patagonian temperate forest and evaluate the influence of egg size on predator guild.

Methods: On different plant species, we placed 108 nests each containing eggs of either Atlantic Canary Serinus canaria or Common Quail Coturnix coturnix, and a model clay egg of equal size to the real egg. Nest predators were identified from the marks left on the clay eggs or by videos recorded using camera traps.

Results: 86% of the nests were predated. Birds, mainly Chimango Caracara Milvago chimango, were the main nest predators. A marsupial, the Monito del Monte Dromiciops gliroides, and rodents also contributed to nest predation. Nest predation rates were similar for both egg sizes but the nest predator guild was different. Birds and rodents preyed on both eggs but the Monito del Monte consumed mainly small eggs.

Conclusion: Egg size did not influence the rate of nest predation but, instead, affected the nest predator guild. Consequently, in order to avoid underestimating the impacts of small predators, egg size should be considered in studies of nest predation.     

Effects of nest-site characteristics and parental activity on cowbird parasitism and nest predation in Brown-and-yellow Marshbirds

ABSTRACT Nest‐site selection and nest defense are strategies for reducing the costs of brood parasitism and nest predation, two selective forces that can influence avian nesting success and fitness. During 2001–2002, we analyzed the effect of nest‐site characteristics, nesting pattern, and parental activity on nest predation and brood parasitism by cowbirds (Molothrus spp.) in a population of Brown‐and‐yellow Marshbirds (Pseudoleistes virescens) in the Buenos Aires province, Argentina. We examined the possible effects of nest detectability, nest accessibility, and nest defense on rates of parasitism and nest predation. We also compared rates of parasitism and nest predation and nest survival time of marshbird nests during the egg stage (active nests) with those of the same nests artificially baited with passerine eggs after young fledged or nests failed (experimental nests). Most nests (45 of 48, or 94%) found during the building or laying stages were parasitized, and 79% suffered at least one egg‐predation event. Cowbirds were responsible for most egg predation, with 82 of 107 (77%) egg‐predation events corresponding to eggs punctured by cowbirds. Nests built in thistles had higher rates of parasitism and egg predation than nests in other plant, probably because cowbirds were most active in the area where thistles were almost the only available nesting substrate. Parasitism rates also tended to increase as the distance to conspecific nests increased, possibly due to cooperative mobbing and parental defense by marshbirds. The proportion of nests discovered by cowbirds was higher for active (95%) than for experimental (29%) nests, suggesting that cowbirds used host parental activity to locate nests. Despite active nest defense, parental activity did not affect either predation rates or nest‐survival time. Thus, although nest defense by Brown‐and‐yellow Marshbirds appears to be based on cooperative group defense, such behavior did not reduce the impact of brood parasites and predators.     

Evaluation of disruptive camouflage of avian cup‐nests

Parent birds employ various strategies to protect their offspring against nest predators. Two well‐researched anti‐nest‐predation strategies involve visual concealment of the nest by way of parental camouflage and egg camouflage. By contrast, camouflage of nest structures is relatively under‐researched, particularly in the case of cup‐nests in trees and bushes. We explored how birds camouflage cup‐nests in nature. Specifically, we tested Hansell’s hypothesis that birds use externally applied pale and white objects such as spider cocoons and lichens to achieve cup‐nest camouflage. To test Hansell’s hypothesis, three complementary experiments were performed: (1) an in situ nest predation experiment; (2) a photo‐based visual search experiment; and (3) contrast analyses using PAT‐GEOM software in IMAGEJ. White paper and chalk spots were used to mimic white objects used by birds in nature. Whereas predation rates in Experiment 1 were not affected by white spots, location rates in Experiment 2 were lower for natural nests with white spots than without white spots. Experiment 3 demonstrated that white spots significantly increased the contrast between different visual elements of nests. It was concluded that white objects can potentially camouflage nests against some nest predators, and that any improved camouflage was probably achieved via disruptive camouflage.     

The response of the Great Reed Warbler Acrocephalus arundinaceus to climate change

We examined long-term responses in the breeding performance of the Great Reed Warblers Acrocephalus arundinaceus to climate change. The study took place in various years from 1970 to 2007. During the study period, mean temperatures in the breeding season of the species increased and precipitation decreased significantly. We found evidence for the significant advancement in both earliest and annual median first-egg-laying dates. This advancement correlated with temperature increases early in the season. The latest first-egg laying dates, however, remained unchanged. Other breeding statistics: clutch size, nest losses, and production of young per nest, did not change significantly over the study period. Precipitation did not affect any of the analysed measures. It is important to note, though, that during dry seasons, the production of young per successful nest was higher. In contrast to some woodland species, the Great Reed Warbler seems to adapt well to climate change by shifting laying dates. The reason for this is probably to optimise food resources.     

The functional significance of multiple nest-building in the Australian Reed Warbler Acrocephalus australis

The vast majority of bird species build a nest in which to breed. Some species build more than one nest, but the function of most multiple nest-building remains unclear. Here we describe the unusual nest-building behaviour of the Australian Reed Warbler Acrocephalus australis , and test experimentally the hypotheses that multiple nest-building is related to individual condition or territory quality, and plays a role in mate assessment. Australian Reed Warblers built two types of nest structures: 'type I' nests, which were used for eggs and nestlings, and 'type II' nests, which were structurally distinct from type I nests, did not support eggs, nestlings or adults and were not essential for successful breeding. The number of type II nests built in each territory varied. Type II nests were only built before breeding had commenced in a territory and females were not observed participating in their construction, supporting a role in female mate choice. Birds provided with supplementary food built significantly more type II nests than control birds. However, supplementary-fed birds did not have greater pairing success, and the addition of further type II nests to territories did not increase the pairing rate or type II nest construction in those territories. There was no relationship between the presence of type II nests and either reproductive success or likelihood of nest predation. We discuss the implications of these results in light of previous suggestions regarding the function of multiple nest-building in birds.