Behaviour of female common cuckoos, Cuculus canorus, in the vicinity of host nests before and during egg laying: a radiotelemetry study

We radiotracked 13 common cuckoo females in the southeastern part of the Czech Republic. Seven females laid eggs in the nests of reed warblers, Acrocephalus scirpaceus, sedge warblers, A. schoenobaenus, and marsh warblers, A. palustris. We observed 53 nest visits, of which 26 involved egg laying. Cuckoos spent significantly more time within 50 m of the host nest on the laying day than on the 5 prelaying days. The vantage point used when parasitizing or visiting a nest was on average four times further from the nest than the closest possible vantage point, but there was a positive correlation between these two distances. Cuckoos spent on average 20 min observing host nests from their vantage points before they visited a nest. Comparison of cuckoos' visits to host nests with and without egg laying revealed no significant differences in the duration of visits or in other measures of behaviour. There was significant variation in behaviour between cuckoos, particularly in the time of day when eggs were laid in host nests. This variation can be attributed to the strong, but not absolute, host and habitat specificity of individuals. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Reed warblers guard against cuckoos and cuckoldry

Previous studies have shown that reed warblers, Acrocephalus scirpaceus, are more likely to reject a cuckoo, Cuculus canorus, egg if they have seen a cuckoo at their nest. This suggests that they would benefit from watching out for cuckoos. We tested whether presentations of a cuckoo mount near the nest (to simulate nest inspection) led to increased nest attendance by the warblers. Cuckoo presentations at completed nests before laying, when males guarded their females closely, led to desertion at 40% of nests before any eggs were laid (there were no desertions after presentations of a jay,Garrulus glandarius , a nest predator). In the remaining cases, there was no effect of the cuckoo on nest attendance before laying began, but a marked increase in male nest attendance (compared with jay and no-presentation controls) on the days the first and second eggs were laid. Cuckoo presentations at the one-egg stage led to the same increase in male nest attendance as did the prelaying presentations. Increased male nest attendance at the one-two-egg stage was not at the expense of mate guarding, because this declined anyway when laying began, and it did not lead to increased paternity loss compared with controls. Overall, 15% of broods had one or two extrapair young (6% of all young extrapair). We conclude that male reed warblers do increase nest guarding in response to cuckoos, but only after their females have begun egg laying, when there are less likely to be costs in lost paternity. Females did not increase nest guarding, perhaps because they need to spend more time foraging during the egg-laying period. Our results suggest that cuckoos should be secretive not only when they lay but also when they monitor host nests beforehand. Copyright 2003 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.      

Accepting unrelated broods helps replacement male yellow-headed blackbirds attract mates

Replacement male yellow-headed blackbirds (Xanthocephalus xanthocephalus)did not destroy broods sired by the previous territorial maleand they showed no aggression toward females with unrelatedbroods. To test whether their tolerance of unrelated young wasmisdirected normal parental care, we removed males from experimentalterritories after primary nests were completed but before secondarynests were initiated. Replacement males fed young that theypresumably had sired in secondary nests and ignored foster youngin primary nests, whereas control males fed young in their primarynests. To identify potential benefits of accepting unrelatedyoung, we analyzed patterns of within-season breeding dispersaland of female settlement on territories following nest lossesto predators. Although some female yellowheads do renest onthe same territory following nest failures, the number of nestsinitiated on territories after a predation event was significantlylower than the number initiated on territories without predationover the same period of time. This implies that late-settlingfemales use the number of active or failed nests and/or thenumber of females on a territory when choosing where to breed.If replacement males that accepted unrelated offspring attractmore new females in the remainder of the current breeding seasonthan infanticidal males, then tolerance of unrelated young byreplacement males may be adaptive in some polygynous birds.     

Mate-sharing costs in polygynous Northern Lapwings Vanellus vanellus

In this study bigamous female Northern Lapwings Vanellus vanellus received significantly less incubation relief from their males than monogamous females. On average, monogamous males spent 34.3% of their time incubating and bigamous males 29.9%. Bigamous males divided their effort between their nests, incubating on average 9.4% on primary nests and 20.5% on secondary nests. Bigamous females compensated for the lack of male relief. Primary females incubated for 71.8% of their time, secondary females for 64.2%, while monogamous females spent 52.7% of their time incubating. As a result, there was no significant difference in total nest attentiveness among nests of different status. Primary and secondary females received equivalent incubation relief from the male. Bigamous males increased their contribution to incubation significantly as the season progressed. A bigamous male's distribution of incubation relief between his females was unrelated to female body mass, or to the degree of asynchrony between primary and secondary females in arrival and laying. Incubation time was significantly, negatively, correlated with total nest attentiveness. Monogamous females spent most time, secondary females spent an intermediate time, and primary females spent the least time on maintenance behaviour (foraging, comfort behaviour, inactivity). No significant differences were found in hatching success among females of different mating status. However, the ratio of unhatched to hatched eggs (i.e. the eggs that remained in the nest at the time of hatching) differed significantly: secondary females hatched a smaller proportion of their eggs than monogamous and primary females.     

Eviction behaviour of the common cuckoo Cuculus canorus chicks

We studied the eviction behaviour of common cuckoo Cuculus canorus chicks by video recording at nests of great reed warblers Acrocephalus arundinaceus and reed warblers Acrocephalus scirpaceus . There were no significant differences in hatching mass and age at first eviction between cuckoos reared by either host. However, mass at eviction had a significant effect on the timing of first eviction event. No significant difference in time required to evict was found between serial intranest eviction events for cuckoos raised by either host. However, "great reed warbler" cuckoos evicted significantly quicker than "reed warbler" cuckoos during particular eviction events. A majority (70%) of "reed warbler" cuckoos evicted during the day, while most "great reed warbler" cuckoos evicted nocturnally (63%). We did not find any effect of the temperature inside or outside the nest on eviction behaviour. Both "great reed warbler" and "reed warbler" cuckoos evicted regardless the fact whether a parent was absent or present at the nest. Interestingly, individual cuckoos were consistent in their eviction behaviour relative to host presence or absence; particular cuckoo chick evicted only when the parents were present or absent from the nest.     

Does Social Mating System Influence Nest Defence Behaviour in Great Reed Warbler (Acrocephalus arundinaceus) Males?

In birds with biparental care, males and females often conflict over how much care to provide to their offspring and it may be substantially influenced by increased level of polygamy. In accordance with sexual conflict theory, males of socially polygynous bird species provide much less care to their nestlings than do males of most socially monogamous species. Most of previous studies, however, have used feeding behaviour as an index for variations in male parental care only. However, this may be skewed if polygynous males compensate for lower feeding assistance through the provision of other parental care such as protection of nests from predators. In this paper, we examine nest defence behaviour in the facultatively polygynous great reed warbler with respect to sex and type of social mating system. We recorded latency to the first arrival, distance from the predator and defensive reaction of each parent towards a human intruder. Socially polygynous males with two simultaneously active nests defended primary females’ nests less vigorously than socially monogamous males, whereas no differences were found between monogamous and primary females. Generally, however, they took a bigger role in nest defence than males in all cases. Our results support an idea that sexual conflict is driven by polygamy and that type of social mating system can influence nest defence behaviour of facultatively polygynous birds. This finding should be taken into consideration when studying nest defence parental care in polygynous mating systems.     

Dynamic risk assessment: does a nearby breeding nest predator affect nest defence of its potential victim?

There is growing evidence that birds are able to discriminate different types of nest intruders and adjust their nest defence behaviour according to intruder dangerousness and distance from the nest (the dynamic risk assessment hypothesis). Here, we tested whether birds’ decisions about nest defence may additionally be affected by an increasing familiarity with a particular nest predator. We tested nest defence responses of great reed warblers Acrocephalus arundinaceus to a nest predator, the little bittern Ixobrychus minutus. Great reed warbler nests located close (≤7 m) to synchronously breeding little bitterns were “neighbour”, other nests were “solitary”. Great reed warbler specific aggression towards a little bittern dummy was much lower (~5-times) at neighbour than solitary nests. In contrast, generalised responses to a control innocuous intruder (the turtle dove, Streptopelia turtur) were statistically identical at neighbour and solitary nests. These patterns are in line with dynamic risk assessment hypothesis. We hypothesise that decreased great reed warbler aggression at neighbour nests also represents a specific behavioural adaptation to nesting in association with the little bittern. Little bitterns breeding closer to great reed warblers showed decreased risks of failure due to predation. However, further research is needed to experimentally test the causal links behind these patterns.     

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.     

Do Hosts Discriminate between Sexually Dichromatic Male and Female Brown‐headed Cowbirds?

Female brood parasites are recognized as threats to reproductive success by many host species. Male brood parasites may accompany females while they search for nests to parasitize and males depredate nests throughout the nesting cycle. Hence, selection may also favour recognition of males. We examined whether two common host species perceive male brown-headed cowbirds ( Molothrus ater ) as brood parasites, as nest predators, or neither. We quantified visits of male cowbirds to nests of yellow warblers ( Dendroica petechia ) and red-winged blackbirds ( Ageliaus phoeniceus ) to assess the frequency with which these host species interact with male cowbirds. Males were observed near nests during hosts' laying and incubating stages, although less frequently than female cowbirds. No visits by cowbirds occurred while parents cared for nestlings. We then presented models of male and female cowbirds plus a non-threatening control to yellow warblers and red-winged blackbirds during laying and nestling periods. If hosts perceive males and females similarly, they should respond more intensely to the cowbird models during the laying period, when nests are most likely to be parasitized. Both species responded similarly to male and female cowbird models during laying, which suggests that hosts view cowbirds of both sexes as threats. The responses of yellow warblers with nestlings to male cowbirds were strongly influenced by the order of model presentation. Warblers first presented with the male cowbird gave much reduced anti-parasite responses than those that first interacted with the female then the male cowbird. These results suggest that yellow warblers recognized male vs. female cowbirds, but that discrimination was not expressed during laying. By contrast, red-winged blackbirds did not discriminate between male and female cowbirds at either nesting stage.     

Responses of great reed warblers Acrocephalus arundinaceus to experimental brood parasitism: the effects of a cuckoo Cuculus canorus dummy and egg mimicry

Egg rejection behaviour towards parasitic eggs was studied in a great reed warbler Acrocephalus arundinaceus population in central Hungary, which was heavily (about 65%) parasitised by the common cuckoo Cuculus canorus . Clutches were experimentally parasitised during the egg-laying period with artificial, moderately mimetic cuckoo eggs or with conspecific eggs that were good mimics of the hosts' eggs. Great reed warblers rejected 76.2% of the artificial cuckoo eggs, mainly by ejection, but accepted most of the conspecific eggs (87.5%). Cuckoo eggs in naturally parasitised clutches were rejected at a lower rate (32%). When, in addition to the egg mimicry experiments, a stuffed cuckoo was placed near the nest, accompanied by the recording of a female cuckoo call, hosts' rejection rate of the artificial cuckoo egg increased from 76% to 96%. The sight of the cuckoo, on the other hand, did not influence host's rejection behaviour when a conspecific egg was used in the experiment. A stuffed collared dove Streptopelia decaocto , accompanied by its call, was used as a control, and did not cause any increased rejection. Great reed warblers were more aggressive towards the cuckoo than to the dove dummy. When the cuckoo eggs in naturally parasitised clutches were exchanged with artificial cuckoo eggs, we observed no increase in the rejection rate. We conclude that great reed warblers in our heavily parasitised population are capable of detecting brood parasitism in their clutch by identifying the parasitic egg. The efficiency of this identification depends mainly on the mimicry of the foreign egg. The sight of the cuckoo at the nest may increase rejection rate by stimulus summation, and this conditional effect is mainly affected by the degree of mimicry of the parasitic egg.     

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.     

Polygyny in the pied flycatcher,Ficedula hypoleuca: a test of the deception hypothesis

The deception hypothesis has been proposed as an explanation for polygyny in the pied flycatcher. According to this hypothesis, already-mated males hide their mating status with polyterritorial behaviour and thereby increase their chances of obtaining a second mate. In a study area at Oslo, Norway, secondary females raised 84% as many fledglings as did concurrent monogamous and primary females. The unmated males sang most of the time near their nest site, whereas the already-mated males frequently disrupted singing for longer periods in their secondary territories to visit their primary nest; such visits to the primary nest occurred both before and after the time of their second mating. The behaviour of the males suggests that deception of females is not an evolutionarily stable strategy, as an observant female would soon discern the male's status. Another difficulty with the deception hypothesis is that secondary females laid larger clutches than primary females. The number of young fledged from secondary nests was not dependent on the distance to the primary nest. The deception hypothesis was not supported by the data, and the reduced reproductive success of secondary females may be explained by the cost of searching for a mate.     

A host-race difference in begging calls of nestling cuckoos Cuculus canorus develops through experience and increases host provisioning

The structure of common cuckoo nestling begging calls differs between the two host-races parasitizing reed warblers (reed warbler-cuckoos) and dunnocks (dunnock-cuckoos; longer syllable duration, lower peak and maximum frequency, narrower bandwidth). Cross-fostering experiments demonstrated that this difference is not genetically fixed but develops through experience. When newly hatched reed warbler-cuckoos were transferred to dunnock nests, they developed begging calls more like those of dunnock-cuckoos, whereas controls transferred to the nests of robins or left to be raised by reed warblers developed calls more typical of reed warbler-cuckoos. We tested the effectiveness of these different calls in stimulating host provisioning by placing in host nests a single blackbird or song thrush nestling (of similar size to a young cuckoo, but lacking its exuberant begging calls); when it begged we broadcast, from a small loudspeaker on the nest rim, recordings of either dunnock-cuckoo or reed warbler-cuckoo begging calls. Playback of dunnock-cuckoo begging calls induced higher levels of provisioning by dunnocks, whereas playback of reed warbler-cuckoo begging calls did so for both reed warblers and robins. We suggest that the young cuckoo (which ejects the host's eggs/chicks and so is raised alone) learns by experience which calls best stimulate host provisioning.     

Untersuchungen an Drossel- und Teichrohrs?nger(Acrocephalus arundinaceus, A. scirpaceus): Bestandsentwicklung, Brutbiologie, ?kologie

Zusammenfassung Von 1973–1978 wurden systematische Beringungen und regelmäßige Nestkontrollen einer Drs-Population im Fränkischen Weihergebiet (Nordbayern) durchgeführt (Auswertung von 487 Nestkarten). Die vorhandene Trs-Population wurde nicht systematisch erfaßt (645 Nestkarten).Der Bestand der einzelnen Teilpopulationen des Drs schwankte im Untersuchungszeitraum; die gesamte Population blieb annähernd konstant.Die Nestabstände benachbarter Drs-Bruten innerhalb eines günstigen Schilfstreifens lagen zwischen 7 m und ca. 300 m. Das kolonieartige Brüten der Trs wird mit Beispielen belegt.Medianer Legebeginn des Drs war der 29. Mai, der des Trs der 13. Juni. Der nach Erreichen des Maximums im Legemuster folgende Abfall war beim Drs deutlich steiler als beim Trs. Die mittlere Gelegegröße des Drs betrug 4,73, die des Trs 3,85 Eier. Bei beiden Arten fand eine Gelegegrößenreduktion mit fortschreitender Brutzeit statt.Das Schlüpfen der Jungen erfolgte beim Drs überwiegend am 12. bis 14. Tag nach Ablage des letzten Eies, beim Trs am 11. bis 13. Die Brutdauer betrug meist 14 (Drs) bzw. 13 (Trs) Tage.Beim Drs waren 59,7 % der Nester erfolgreich. Der Ausfliegeerfolg, bezogen auf erfolgreiche Nester, betrug 73,2 %, der Gesamtbruterfolg demnach 43,7 %. Beim Trs ergaben sich entsprechend die Werte 66,6 %, 82,9 % und 55,2 %. Auch die durchschnittliche Anzahl flügger Jungvögel pro Brutnest lag beim Drs mit 2,00 etwas niedriger als beim Trs mit 2,15. Als Reproduktions-rate des Drs wurde ein Wert von 2,24 flüggen Jungen pro errechnet. Für den Trs wird die Reproduktionsrate wesentlich höher geschätzt.Die Verluste wurden nach Ursachen aufgeschlüsselt, wobei besonders verglichen mit gleichaltrigen Trs die vielfach größere Empfindlichkeit nestjunger Drs gegen Regen und Kälte auffiel.In zwei Fällen konnten für Drs- Zweitbruten mittels Beringung nachgewiesen werden. Beobachtungen an Trs gaben zu Vermutungen von Zweitbruten bei dieser Art Anlaß.Bigamie wurde beim Drs mehrfach mittels Farbberingung nachgewiesen. Aus den Nestabständen konnte im Untersuchungsgebiet nicht auf monogames oder polygames Verhalten der Drs geschlossen werden. Es werden Angaben über Alter und Verhalten polygamer in verschiedenen Jahren gemacht. Paarzusammenhalt am Vorjahresbrutplatz wurde beim Drs mittels Beringung einmal nachgewiesen.Die meisten überlebenden der als Brutvögel beringten Drs kehrten ins Untersuchungsgebiet zurück, von den überlebenden nestjung beringten dagegen etwa ein Drittel. 3 nestjung beringte Trs wurden nach 1 bzw. 2 Jahren im Untersuchungsgebiet zur Brutzeit kontrolliert.Ein Drittel der Drs-Population stammte aus dem Untersuchungsgebiet. 2 nestjung beringte aus 78 km und 500 km Entfernung wurden als Brutvögel kontrolliert. Alter der Brutvögel 1–9 Jahre.An Beispielen wird die räumliche und zeitliche Einnischung beider Arten beschrieben.

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Studies onAcrocephalus arundinaceus andscirpaceus: Population trends, breeding biology, and ecology

Summary Results of 6 years (1973–1978) of systematic ringing and regular nest controls of a great reed warbler population in Northern Bavaria are given (data of 487 nests) as well as results on a population of the reed warbler (data of 645 nests).Numbers of great reed warblers fluctuated in different parts of the study area. The whole population, however, remained fairly constant.Data on the arrival of males in the breeding area are given.Distances between neighbouring nests of great reed warblers varied from 7 to about 300 m. Differences in nest densities in the reed warbler could be found.The mean first egg laying dates in the great reed warbler and the reed warbler were May 29 and June 13 respectively. The great reed warbler showed a distinct steeper decrease in its egg laying pattern than the smaller species. Average clutch size in the great reed warble was 4.73 eggs and 3.85 eggs in the reed warbler. In both species clutch size decreased during the season.Great reed warbler nestlings hatched on the 12th to 14th day after the last egg had been laid, reed warbler nestlings on the 11th to 13th day. The incubation period was mainly 14 days in the great reed warbler and 13 days in the reed warbler.In the great reed warbler 59.7 % of the nests were successful. The fledging success of successful nests was 73.2 %, accordingly the total nest success was 43.7 %. The corresponding data in reed warbler were 66.6 %, 82.9 % and 55.2 %. On average great reed warblers produced 2.00 fledglings per clutch, reed warblers 2.15. In the great reed warbler a reproduction rate of 2.24 fledglings per female was calculated. The reproduction rate in reed warbler was estimated substantially higher.Great reed warbler nestlings were much more sensitive to rain and cold weather than reed warbler nestlings of the same age.Two great reed warbler males were proved to make a second brood. The same is supposed for the other species but could not be proved so far.Polygyny was proved several times in the great reed warbler. Age and behaviour of polygynous males in different years are reported. Two great reed warblers were found breeding with their former mates at last year's breeding place.Most of the great reed warblers ringed as breeding birds returned into the study area. Nearly one third of the great reed warbler nestlings returned for breeding. Three reed warblers ringed as nestlings could be controlled in the study area during breeding period after 1 year and 2 years respectively.Distances of returned great reed warblers in relation to their birth places and their former breeding places are specified.One third of the great reed warbler population originates from the study area. Two females breeding in the study area were ringed as nestlings 78 km and 500 km apart.One-year-old to nine-year-old great reed warblers were found breeding. Data on the age composition of breeding birds are given.Plant species supporting the nests of great reed warbler and reed warbler were investigated. Differences in the spatial and temporal habitat selection of both species are described.

     

Do females adjust the sex of their offspring in relation to the breeding sex ratio?

When the adult sex ratio differs between years in local populations, but still is predictable between adjacent years, it has been proposed that the best strategy would be to bias the offspring sex ratio in favour of the rare sex. We tested this hypothesis using a data set of great reed warbler offspring, sexed by molecular techniques, that were collected over 11 breeding seasons at two adjacent reed marshes. Three important assumptions for this hypothesis are fulfilled in the studied great reed warbler population. First, a substantial proportion of great reed warblers are living in small local populations where sex ratio distortions would be sufficiently large and common. Second, breeding adults and their offspring return to breed in the local population to a high degree. Third, females have a possibility to assess the breeding sex ratio before laying their eggs. At our study site, the breeding sex ratio was positively correlated between successive years. However, contrary to our prediction, female great reed warblers seemed not to adjust their offspring sex ratio in relation to the local breeding sex ratio.     

Predation risk affects trade-off between nest guarding and foraging in Seychelles warblers

The fitness costs of egg loss for Seychelles warblers (Acrocephalus sechellensis)on Cousin Island are considerable because warblers have a single-eggclutch and no time to lay a successful replacement clutch. Onthe islands of Cousin and Cousine, with equal densities of Seychellesfodies (Foudia sechellarum), nearly 75% of artificial eggs placedin artificial nests were predated by fodies after 3 days. OnAride Island with no fodies present, loss of artificial eggswas not observed. Female warblers incubate the clutch, and malewarblers guard the clutch when females are absent. Deterrenceof fodies by male warblers is efficient: loss rate of eggs fromunattended warbler nests was seven times as high as from attendednests, and the more nest guarding, the lower the egg loss andthe higher the hatching success. Egg loss is independent ofthe amount of incubation by females. There is no trade-off betweenincubating and foraging by females. Nest guarding competes withforaging by males, and this trade-off has a more pronounced effecton egg loss when food availability is low. The transfer of breeding pairsfrom Cousin to either Cousine with egg-predating fodies or toAride without fodies allowed us to experimentally investigatethe presumed trade-off between nest guarding and foraging. OnCousine, individual males spent the same amount of time nestguarding and foraging as on Cousin, and egg loss was similarand inversely related to time spent nest guarding as on Cousin.Males that guarded their clutch on Cousin did not guard theclutch on Aride but allocated significantly more time to foragingand gained better body condition. Loss of warbler eggs on Aridewas not observed. Time allocation to incubating and foragingby individual females before and after both translocations remainedthe same.     

No evidence for recognition errors in Acrocephalus warblers

Failure to recognise own eggs (recognition errors) may be an important selective force behind acceptance of parasitic eggs, leading to a balance between rejecters and acceptors in a host population (the equilibrium hypothesis). We predicted that recognition errors should occur frequently among host species with intermediate rejection rates, whose rejection behaviour shows many conditional responses. The reed warbler Acrocephalus scirpaceus and great reed warbler A. arundinaceus fulfil these requirements. These two species were therefore used in an experiment where host birds were exposed to a common cuckoo Cuculus canorus dummy, either <2 m or 5–10 m from the nest, at fishponds in southern Moravia (Czech Republic). The hosts responded to the cuckoo dummy, great reed warblers being much more aggressive than reed warblers, and both species being more aggressive towards the dummy when it was close to the nest than when it was farther away. We furthermore predicted that there should be more eggs rejected (ejected or nest abandoned) due to recognition errors among hosts exposed to a dummy close to the nest than among both those exposed to a dummy farther away from the nest and towards controls not exposed to cuckoo dummies. When comparing egg loss between groups of birds that were exposed to a cuckoo dummy with those that were not, we found no significant difference. However, partial egg loss was frequent among hosts in the studied population, most probably due to cuckoo depredation. We discuss why there were no detectable recognition errors in the studied population, when other researchers have claimed to have found such errors in host populations elsewhere.     

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.     

Social behaviour ofRopalidia fasciata (Hymenoptera: Vespidae) females on satellite nests and on a nest with multiple combs

The social behaviour ofRopalidia fasciata females on 3 satellite nests and on a nest with multiple, independent combs was observed. Many females often visited satellite nests, and even dominant foundresses, who usually spent more of their time on the nest, became active when satellite nests were being constructed. Three foundresses laid eggs on a satellite nest and eggs laid by 2 of these (who performed foraging) survived. On another satellite nest, only the dominant foundress laid an egg which survived. On a nest consisting of 2 independent combs, females frequently shifted between the 2 combs even after the emergence of many adults. Constructions of satellite nests and of multiple independent combs are considered to be adaptive for this species living in Okinawa, where most of nests are destroyed by frequent typhoons or abandoned after predation by ants.