Experimentally Simulating Paternity Uncertainty: Immediate and Long-Term Responses of Male and Female Reed Warblers Acrocephalus scirpaceus

In many socially monogamous species, both sexes seek copulation outside the pair bond in order to increase their reproductive success. In response, males adopt counter-strategies to combat the risk of losing paternity. However, no study so far has tried to experimentally prove the function of behaviour for paternity assurance. Introducing a potential extra-pair partner during the female fertile period provides a standardised method to examine how pair members respond immediately (e.g. increase mate guarding or copulation frequency) or long term (e.g. later parental investment and paternity uncertainty). In this study on a socially monogamous passerine species, we experimentally confronted pairs of reed warblers with a conspecific male (caged male simulating an intruder) during egg-laying. Our results revealed that occurrence of an intruder during that period triggered aggression against the intruder, depending on the presence of the female. The male territory owner also attacked the female partner to drive her away from the intruder. Thus territory defence in reed warblers also serves to protect paternity. The increase in paternity uncertainty did not affect later paternal investment. Paternal investment was also independent of the actual paternity losses. In females, the experiment elicited both, immediate and long-term responses. E.g. female copulation solicitations during the intruder experiment were only observed for females which later turned out to have extra-pair chicks in their nest. In relation to long term response females faced with an intruder invested later less in offspring feeding, and had less extra-pair chicks in their nests. Extra-pair paternity also seems to be affected by female quality (body size). In conclusion female reed warblers seem to seek extra-pair fertilizations but we could demonstrate that males adopt paternity assurance tactics which seems to efficiently help them to reduce paternity uncertainty.     

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.     

Enemy Recognition of Reed Warblers (Acrocephalus scirpaceus): Threats and Reproductive Value Act Independently in Nest Defence Modulation

Organisms should respond more aggressively towards species perceived as a danger to their offspring, but intensity of defence may be gauged by the value of current offspring weighed against the value of future reproductive opportunities. We tested whether defensive responses of nesting reed warblers (Acrocephalus scirpaceus) are the result of an interaction effect between the type of stimulus confronted and the value of the warbler’s nesting attempt. We quantified the ability of reed warblers to discriminate among brood parasites, nestling predators and non‐threatening species at different stages of the breeding cycle. We also determined whether variables that influence the value of offspring, such as time of season, size and age of clutch or brood, and time of day and number of visits to the nest, explain variation in the intensity of defence recorded during the egg and nestling stages. Responses to the three stimuli differed significantly, as reed warblers consistently directed their mobbing calls and attacks towards parasites, whereas they were less conspicuous when confronted with models of predators. Reed warblers modulated their responses towards each stimulus in accordance with the threat each posed at a specific nesting stage, whereas they were not affected by other variables relative to their reproductive potential. The churr call, however, was uttered independently of the stimulus, as it was triggered by the mere presence of nestlings in the nest.     

Mate desertion by male Great Reed Warblers Acrocephalus arundinaceus at the end of the breeding season

Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains.     

Factors affecting the cost of polygynous breeding for female Great Reed Warblers Acrocephalus arundinaceus

The male's role in feeding young and his effect on the mortality of eggs and nestlings of the Great Reed Warbler Acrocephalus arundinaceus were studied in Kahokugata, central Japan, during eight breeding seasons. Three potential costs of polygynous breeding for females were examined:(i) a reduction of male parental care per brood, (ii) an attraction of predators due to concentration of nests, and (iii) an increase of unfertilized eggs due to the reduced frequency of copulation per female. Only the first cost was found to occur:polygynous males fed their young, especially of their second broods, less frequently than monogamous ones. The lowered paternal feeding frequency, however, did not increase the mortality by starvation in second-hatched broods. This was because the warm climate emancipated females from brooding and enabled them to compensate for the deficiency of feeding by males. The paper discusses possible roles of the staggering of the time of laying among harem mates and the shift of breeding status of females caused by nesting failure, in reducing potential costs of polygynous breeding for females.     

Mate desertion by male Great Reed Warblers Acrocephalus arundinaceus at the end of the breeding season

Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains.     

Spring nocturnal migration of Reed Warblers Acrocephalus scirpaceus: departure, landing and body condition

Nocturnal migration of Reed Warblers Acrocephalus scirpaceus was studied by trapping with 'high nets' on the Courish Spit (Eastern Baltic) during spring 1998–2000. In spring, Reed Warblers left the stopover site between 45 and 240 min after sunset (median 84 min), although 85% of birds took off between 45 and 120 min after sunset. Birds did not arrive until the fifth hour after sunset; 67% of birds ended their nocturnal flights in the penultimate hour before sunrise, i.e. at dawn. At the moment of migratory departure, the average Reed Warbler body mass was 12.79 ± 0.66 g ( n  = 60). Average body mass of birds ending migratory flight was 11.69 ± 0.67 g ( n  = 18). The difference was highly significant. However, more than half of the birds completed migratory flights with a considerable fuel load, and some even had energy stores sufficient for a migratory flight on the next night. The spring migratory strategy of Reed Warblers over Central and Northern Europe probably includes a succession of short migratory flights (4–6 h) during several subsequent nights with 1-day stopovers.     

Effects of mate removal on the behaviour and reproductive success of Reed Warblers Acrocephalus scirpaceus

The Reed Warbler Acrocephalus scirpaceus is a largely monogamous insectivorous passerine in which males and females provide equal care by day to eggs and chicks. Polygyny occurs occasionally, with males leaving one female unaided. When females were temporarily removed from three recently-completed clutches their males deserted and resumed the high song levels typical of unmated males. Males may desert either because they are physically incapable of incubation or because the energy expenditure needed for a male to return to an equivalent stage in the breeding cycle is much lower than for a female to do so. Widowed females ( n = 7 ), however, continued the breeding attempt alone, with similar incubation levels but higher provisioning rates than those of control females. In three out of four mid-season broods raised by lone females all fertile eggs were reared to healthy fledglings (in the fourth brood the female died), while only one of four late-season nests produced any fledglings (which were underweight). Late-season control nests were as successful as earlier ones. Loss of male help led to starvation of chicks, but caused no adverse effects during incubation. This explains the small changes in widows' sitting levels during incubation, but much greater effects after hatching. Females may need male help to rear late broods (but not early broods) as days are shorter and food is scarcer. Males may normally help at nests, even those in the mid-season, because in stressful spells (even for a few days) such help is vital for successful breeding but in good periods it costs the male little.     

Nest Predation Avoidance: an Alternative Explanation for Male Incubation in Acrocephalus melanopogon

In the monogamous moustached warbler, male incubation changes from predictably variable (it is dependent on ambient temperature and time of day in April) to high average levels across the day (with no predictor variables in May) as the season progresses. In contrast, females contribute the constant incubation component from April to May. This paper investigates possible explanations for the change in male incubation effort involving changing risks to either (1) embryonic survival within the egg, and/or (2) egg predation. Using egg temperature readouts, the probability of reaching the 25 °C thermal threshold (below which embryonic development ceases) across the season against the probability of predator sightings 0–15 m from the nest was calculated. The results show an inverse relationship between these two risks. During April, male incubation correlates with egg cold stress and changeovers between males and females occur prior to egg cooling below the thermal stress line. During May, the risk of predation increases. The results show increased predator encounter rates from April to May and active nest defense by the incubating parent. Furthermore, high male incubation reduces brood predation. Selection for reduction of the costs of laying replacement clutches (after predation) is suggested given high male incubation and infrequent male-female changeovers during midday, when egg temperatures are highest, with direct benefits to females of increased foraging. Thus, the shift in male incubation across the season may be explained by minimization of changing risk to offspring survival.     

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.     

Stable isotope ratios in winter‐grown feathers of Great Reed Warblers Acrocephalus arundinaceus,Clamorous Reed Warblers A. stentoreus and their hybrids in a sympatric breeding population in Kazakhstan

Analyses of the stable isotope composition of feathers can provide significant insight into the spatial structure of bird migration. We collected feathers from Great Reed Warblers Acrocephalus arundinaceus, Clamorous Reed Warblers A. stentoreus and a small sample of their hybrids in a sympatric breeding population in Kazakhstan to assess natural variation in stable isotope signatures and delineate wintering sites. The Great Reed Warbler is a long‐distance migrant that overwinters in sub‐Saharan Africa, whereas the Clamorous Reed Warbler performs a short‐distance migration to the Indian sub‐continent. Carbon (δ¹³C), nitrogen (δ¹⁵N) and deuterium (δD) isotope signatures were obtained from winter‐grown feathers of adult birds. There were highly significant differences in δD and less significant differences in δ¹³C between Great and Clamorous Reed Warblers. Thus, our results show that the stable isotope technique, and in particular the deuterium (δD) signal, resolves continental variation in winter distribution between these closely related Acrocephalus species with sympatric natal origin. The isotope signatures of hybrid Great × Clamorous Reed Warblers clustered with those of the Great Reed Warblers. Hence, a parsimonious suggestion is that the hybrids undergo moult in Afrotropical wintering grounds, as do the Great Reed Warblers. The observed δD values fell within the range of expected values based on available precipitation data collected at precipitation stations across the wintering continents of each species. However, the power to predict the winter origin of birds in our study system using these data was weak as the expected values ranged widely at this broad continental scale.     

Early settling the following spring: a long-term benefit of mate desertion by male Great Reed Warblers Acrocephalus arundinaceus

In a population of the Great Reed Warbler Acrocephalus arundinaceus in central Japan 33 cases of mate desertion by males were recorded during eight breeding seasons. Thirty of these occurred at the end of the breeding season. The absence of the male parent during the nestling period affected neither the frequency of nestling starvation nor the return of females. Eight deserters were confirmed to have begun moulting prior to the fledging of their young. Males which had abandoned their territory relatively early in the summer tended to settle earlier and to be polygynous the following spring. As earlier settling is an important factor influencing polygyny in males, an increased chance of early settling the following season can be regarded as a long-term benefit of mate desertion.     

Longer is fatter: body mass changes of migrant Reed Warblers (Acrocephalus scirpaceus) staging at Eilat,Israel

Ecological barriers are the riskiest phases of the annual migrations for migratory birds. Comparatively little field data exists pertaining to the ability of migratory birds to prepare for the challenges of crossing ecological barriers, or their ability to recuperate afterward. Migrating Reed Warblers (Acrocephalus scirpaceus) were captured in Eilat, Israel, during their spring and autumn migrations. Data on spring and autumn body masses, their inter-annual variation, and the pattern of body mass increase were analysed. The birds show a significant inter-annual variation in their body mass and body condition index in both seasons, which is consistent with the data from other sites and for other passerine species. During stopovers, mass gain occurred in both seasons. Birds in poor initial condition, and those that stop over for a longer period of time, gained more body mass faster. In spring, but not in autumn, the progress of the season was also an important factor; late-arriving birds gained more fuel faster. The average rate of fuel gain was 0,157g·day^?1 ± 0.018 SE.     

Responses of breeding Reed Warblers Acrocephalus scirpaceus to mounts of Sparrowhawk Accipiter nisus, Cuckoo Cuculus canorus and Jay Garrulus glandarius

Mounts of a Cuckoo Cuculus canorus , a Sparrowhawk Accipiter nisus and a Jay Garrulus glandarius were presented at nests of Reed Warblers Acrocephalus scirpaceus at all breeding stages. Response strength could best be classified according to approach distance (to the mount) and vocalizations used. Warblers reacted much more aggressively to a mount on the nest than to one 3 m adjacent; they approached much more closely, were less likely to sing but often gave a frenzied-sounding rasp (which was never given to an adjacent mount). Reaction was more aggressive to a Cuckoo, which was often attacked, than to a Sparrowhawk, of which they were wary; response to a Jay was intermediate. Reaction was more aggressive after the clutch had been completed than before. After the brood had fledged, parents still responded strongly to the Jay and Sparrowhawk, but responded to the Cuckoo only briefly before ignoring it. These results are consistent with the Reproductive Value-Stimulus Value hypothesis. They also demonstrate that Reed Warblers can tell Cuckoos from Sparrowhawks, as can many non-host species. The close resemblance of these two species is often suggested to be mimicry of the Sparrowhawk by the Cuckoo but, if this is so, it is not successful. Alternatively, the similarity could be mimicry to reduce predation on the Cuckoos themselves, a chance resemblance, or due to similar selective forces acting on both species, as each would presumably benefit from reduced conspicuousness.     

Provisioning of nestling Cuckoos Cuculus canorus by Reed Warbler Acrocephalus scirpaceus hosts

Reed Warblers Acrocephalus scirpaceus fostering a single nestling Cuckoo Cuculus canorus bring food to it at roughly the same rate as they do to an average-sized brood (three or four) of their own young. The food brought, mostly flies and beetles, is also similar. We conclude that the Cuckoo does not provide a supernormal stimulus. We show that Reed Warblers, given experimentally-enlarged broods of seven or eight, can substantially increase their feeding rate. This raises the question of why the young Cuckoo does not exploit this 'spare' feeding capacity of the Reed Warbler hosts. We offer three explanations', (i) that the increased begging necessary would attract predators, (ii) that the young Cuckoo is unable to grow faster, and (iii) that it would not be to the advantage of a young Cuckoo, dependent on its foster parents for about 5 weeks (cf. 3 weeks for Reed Warbler young), to provoke a feeding rate that the warblers could not sustain.     

European Cuckoo Cuculus canorus parasitism and host's rejection behaviour in a heavily parasitized Great Reed Warbler Acrocephalus arundinaceus population

An unusually high frequency (64%) of European Cuckoo Cuculus canorus parasitism was found in Great Reed Warbler Acrocephalus arundinaceus clutches in central Hungary. Sixty-four per cent of the parasitized clutches contained one Cuckoo egg, 23% contained two, 10% had three and 3% had four. This means that 58% of the Cuckoo eggs were found in multiply parasitized clutches. In multiple parasitism the laying second Cuckoo removed an egg from the clutch randomly, so preferred neither the host eggs, nor the concurrent Cuckoo egg. Host response towards the parasitic eggs showed 66% acceptance, 12% ejection, 20% desertion and 2% egg burial. We found great variation in both the host and the parasitic egg colour and pattern. This reduces the chance that the parasitic egg's appearance matched that of the hosts' but, in spite of this, almost perfect mimesis was found in 28% of the Cuckoo eggs. Poorly mimetic Cuckoo eggs were more frequently rejected by Great Reed Warblers than parasite eggs that were very similar to the host eggs. This high level of mimicry sometimes makes it difficult for the observer to identify the parasitic egg, especially when it is similar in size to the host eggs. It is also difficult for the host, as shown by the relatively high recognition error and ejection cost.     

三个东方大苇莺种群大杜鹃寄生率的变异

东方大苇莺Acrocephalus orientalis是大杜鹃Cuculus canorus的主要寄主之一。本文对东方大苇莺的3个地理种群进行杜鹃寄生率的时空比较。发现不同东方大苇莺种群被大杜鹃的巢寄生率在21.4%和65.5%之间,差异显著;不过,地理位置相近的两个种群在巢寄生率上则没有显著差异。另外,同一地理种群的巢寄生率年间也存在显著差异。     

Predation on Moose Calves by European Brown Bears

Abstract: In North America, brown bears (Ursus arctos) can be a significant predator on moose (Alces alces) calves. Our study in Sweden is the first in which brown bears are the only predator on moose calves. Bears and moose occurred at densities of about 30/1,000 km² and 920/1,000 km², respectively, and bears killed about 26% of the calves. Ninety-two percent of the predation took place when calves were <1 month old. Bear predation was probably additive to other natural mortality, which was about 10% in areas both with and without bears. Females that lost their calves in spring produced more calves the following year (1.54 calves/F) than females that kept their calves (1.11 calves/F), which reduced the net loss of calves due to predation to about 22%.