Nest site selection by a neotropical swarm-founding wasp: seasonal alternation of nest orientation

Nest orientation in social insects has been intensively studied in warmer and cooler climates, particularly in the northern hemisphere. Previous studies have consistently shown that species subjected to these climatic conditions prefer to select mostly southern locations where the nests can gain direct sunlight. However, very little is known on nest orientation in tropical and subtropical social insects. We studied nest orientations initiated by swarms throughout a year in a Brazilian swarm-founding wasp, Polybia paulista von Ihering (Hymenoptera: Polistinae). Swarms selected various orientations as nest sites, but there was a particular trend in that swarms in the winter period (May–August) preferred to build northward-facing nests. This preference is opposite from that of social wasps observed in the northern hemisphere. Colonies of this species can potentially last for many years with continuous nesting, but nesting activities of colonies during the winter are severely limited due to cool temperature and a shortened day length. Northward-facing nests are warmer through the gain of direct solar heat during the winter period; consequently, choosing northward-facing sites may be advantageous for swarms in terms of a shortened brood development and shortened time needed to increase metabolic rates during warm-up for flight.     

Heat or insulation: behavioral titration of mouse preference for warmth or access to a nest

In laboratories, mice are housed at 20–24°C, which is below their lower critical temperature (≈30°C). This increased thermal stress has the potential to alter scientific outcomes. Nesting material should allow for improved behavioral thermoregulation and thus alleviate this thermal stress. Nesting behavior should change with temperature and material, and the choice between nesting or thermotaxis (movement in response to temperature) should also depend on the balance of these factors, such that mice titrate nesting material against temperature. Naïve CD-1, BALB/c, and C57BL/6 mice (36 male and 36 female/strain in groups of 3) were housed in a set of 2 connected cages, each maintained at a different temperature using a water bath. One cage in each set was 20°C (Nesting cage; NC) while the other was one of 6 temperatures (Temperature cage; TC: 20, 23, 26, 29, 32, or 35°C). The NC contained one of 6 nesting provisions (0, 2, 4, 6, 8, or 10g), changed daily. Food intake and nest scores were measured in both cages. As the difference in temperature between paired cages increased, feed consumption in NC increased. Nesting provision altered differences in nest scores between the 2 paired temperatures. Nest scores in NC increased with increasing provision. In addition, temperature pairings altered the difference in nest scores with the smallest difference between locations at 26°C and 29°C. Mice transferred material from NC to TC but the likelihood of transfer decreased with increasing provision. Overall, mice of different strains and sexes prefer temperatures between 26–29°C and the shift from thermotaxis to nest building is seen between 6 and 10 g of material. Our results suggest that under normal laboratory temperatures, mice should be provided with no less than 6 grams of nesting material, but up to 10 grams may be needed to alleviate thermal distress under typical temperatures.     

Nest box design for a changing climate: The value of improved insulation

Mean air temperatures and the frequency, intensity and duration of extreme weather events such as heatwaves are increasing due to climate change. Nest boxes experience more variable and extreme temperatures than natural cavities, which may reduce survival and reproductive success of the species which utilize them, but little is known about the factors which drive nest box temperature profiles. We quantified the potential for retrofitted insulation on nest boxes to modify internal temperatures and to mimic the thermal characteristics of natural cavities more closely. We tested three types of materials with insulative or reflective properties which were easy to retrofit to nest boxes: 3‐cm‐thick polystyrene, pleated foil batts and reflective paint. We found that polystyrene and foil batts reduced mean nest box temperatures during the day by 0.31 ± 0.01°C and 0.17 ± 0.01°C, respectively (but up to 5.84°C and 4.02°C). The effects of all insulation types were dependent on the time of day, and only polystyrene had a significant effect at night, with a greater capacity to retain heat (mean 0.21 ± 0.01°C warmer). Contrary to expectations, reflective paint caused a small increase in temperature during the late afternoon. In our study, the temperature modulation provided by insulation was able to match or exceed that due to variation in nest location and surrounding vegetation canopy cover. Our findings show that polystyrene and foil batts may offer effective and tractable means to mitigate the effects of extreme temperatures in nest boxes and thereby help achieve temperature profiles more similar to natural cavities.     

Nest timing,nest site selection and nest structure in a high latitude population of Bearded Reedlings Panurus biarmicus

Capsule: Bearded Reedlings Panurus biarmicus show consistent nest timing, select old, compacted areas of reed when positioning their nests, and may adjust nest structure in relation to local reed characteristics and temperature.

Aims: To investigate the nest timing, nest site selection and nest structure of a rare and elusive passerine, the Bearded Reedling at the northern limit of this species’ range.

Methods: A sample of Bearded Reedling nests from the Tay Reedbeds in Scotland were located and monitored with regard to the timing of nesting, fate, fine-scale habitat characteristics and nest structure.

Results: First egg dates and brood sizes were consistent between years of the study despite variation in spring temperatures. Bearded Reedlings nested within unmanaged patches of reed, positively selecting deep leaf litters and compacted reed. Attributes of nest structure, namely internal and external diameter, were influenced by nest site characteristics and local temperature.

Conclusion: Despite a limited sample size, the study suggests that reedbed management should ensure adequate areas of old, dry and unmanaged reed are available when aiming to encourage breeding Bearded Reedlings. Additionally, the apparently flexible structure of the nest may assist this species when coping with changeable climatic conditions.     

Nest desertion by Grey Fantails during nest building in response to perceived predation risk

ABSTRACT Grey Fantails (Rhipidura albiscapa), a common Australian flycatcher, commonly desert their nests before egg‐laying. We tested the hypothesis that Grey Fantails desert incomplete nests in response to the attention of predators by placing a mounted Pied Currawong (Strepera graculina), a common nest predator, near fantail nests that were under construction. As a control, we placed a mounted King Parrot (Alisteris scapularis), a nonpredatory bird similar in size to Pied Currawongs, near other fantail nests. Four of six female fantails (67%) deserted incomplete nests in response to the presentation of the Pied Currawong. In contrast, none of the seven females presented with a mounted King Parrot deserted. Female Grey Fantails may use the attention of a predator at the nest during the building stage as a cue to desert. Such desertion may be adaptive for Grey Fantails because currawongs are large predators, making successful nest defense unlikely, and they also present considerable risk to adults. In addition, fantails may raise multiple broods during a breeding season and, therefore, have a high renesting potential.     

Nest relocation in the slavemaking ants Formica subintegra and Formica pergandei: a response to host nest availability that increases raiding success

Social insects typically occupy spatially fixed nests which may thus constrain their mobility. Nevertheless, colony movements are a frequent component of the life cycle of many social insects, particularly ants. Nest relocation in ants may be driven by a variety of factors, including nest deterioration, seasonality, disturbances, changes in microclimate, and local depletion of resources. The colony movements of slavemaking ants have been noted anecdotally, and in recent studies such relocations were primarily attributed to nest deterioration or shifts to overwintering locations. In this study we explore nest relocations in large colonies of formicine slavemakers which occupy stable and persistent earthen nest mounds. We investigate the hypothesis that colony relocations of these slavemakers are best explained by efforts to improve raiding success by seeking areas of higher host availability. Five summers of monitoring the raiding behavior of 11–14 colonies of the slavemakers Formica subintegra and Formica pergandei revealed relatively frequent nest relocations: of 14 colonies that have been tracked for at least three of 5 years, all but one moved at least once by invading existing host nests. Movements tended to occur in the middle of the raiding season and were typically followed by continued raiding of nearby host colonies. Spatial patterns of movements suggest that their purpose is to gain access to more host colonies to raid: the distance moved is typically farther than the mean raiding distance before the move, which may indicate an effort to escape their local neighborhood. Furthermore, the mean distance of raids after relocation is shorter than the distance before relocation. For many slavemaking ant colonies, particularly those on the verge of relocating, raiding distance increased as the raiding season progressed. In addition, movements tended to be toward areas of higher local host density. Nest relocation is likely an important component of the ecology of slavemaking ants that contributes to the dynamic nature of their interaction with the host ant population.     

Nest predation increases with parental activity: separating nest site and parental activity effects.

Alexander Skutch hypothesized that increased parental activity can increase the risk of nest predation. We tested this hypothesis using ten open-nesting bird species in Arizona, USA. Parental activity was greater during the nestling than incubation stage because parents visited the nest frequently to feed their young during the nestling stage. However, nest predation did not generally increase with parental activity between nesting stages across the ten study species. Previous investigators have found similar results. We tested whether nest site effects might yield higher predation during incubation because the most obvious sites are depredated most rapidly. We conducted experiments using nest sites from the previous year to remove parental activity. Our results showed that nest sites have highly repeatable effects on nest predation risk; poor nest sites incurred rapid predation and caused predation rates to be greater during the incubation than nestling stage. This pattern also was exhibited in a bird species with similar (i.e. controlled) parental activity between nesting stages. Once nest site effects are taken into account, nest predation shows a strong proximate increase with parental activity during the nestling stage within and across species. Parental activity and nest sites exert antagonistic influences on current estimates of nest predation between nesting stages and both must be considered in order to understand current patterns of nest predation, which is an important source of natural selection.     

Nest predation and nest site selection among Eiders Somateria mollissima: the influence of gulls

Hooded Crows Corvus cornix, Great Black-backed Gulls Larus marinus and Herring Gulls L. argentatus were the main nest predators in an Eider population in southwest Sweden. The clutch sizes of Eider nests within gull colonies did not differ from those outside gull colonies. The proportion of Eider nests destroyed by predators was significantly lower within than outside gull colonies, especially on islands with Lesser Black-backed Gulls L. fuscus. Although the difference was not significant, the survival time of simulated Eider nests was higher within than outside gull colonies. On Eider islands with gull colonies, foraying crows spent more time within the colony area than expected by chance. However, crows apparently avoided an area around each gull nest, and we suggest that the colonies, to some extent, protected Eider nests against predation. The density of Eider nests was higher on gull islands than on gull- free islands, and higher within than outside the gull colonies. However, the association with gulls was weak compared to that displayed by some other waterfowl.     

Nest site attributes and temporal patterns of northern flicker nest loss: effects of predation and competition

To date, most studies of nest site selection have failed to take into account more than one source of nest loss (or have combined all sources in one analysis) when examining nest site characteristics, leaving us with an incomplete understanding of the potential trade-offs that individuals may face when selecting a nest site. Our objectives were to determine whether northern flickers (Colaptes auratus) may experience a trade-off in nest site selection in response to mammalian nest predation and nest loss to a cavity nest competitor (European starling, Sturnus vulgaris). We also document within-season temporal patterns of these two sources of nest loss with the hypothesis that flickers may also be constrained in the timing of reproduction under both predatory and competitive influence. Mammalian predators frequently depredated flicker nests that were: lower to the ground, less concealed by vegetation around the cavity entrance and at the base of the nest tree, closer to coniferous forest edges and in forest clumps with a high percentage of conifer content. Proximity to coniferous edges or coniferous trees increased the probability of nest predation, but nests near conifers were less likely to be lost to starlings. Flickers may thus face a trade-off in nest site selection with respect to safety from predators or competitors. Models suggested that peaks of nest predation and nest loss to eviction occurred at the same time, although a competing model suggested that the peak of nest loss to starlings occurred 5 days earlier than the peak of mammalian predation. Differences in peaks of mammalian predation and loss to starlings may constrain any adjustment in clutch initiation date by flickers to avoid one source of nest loss.     

Nest re-use and communal nesting inMicrothurge corumbae (Hymenoptera,Megachilidae), with special reference to nest defense

Summary Observations on the nesting activities ofMicrothurge corumbae, carried out at the University Campus of Ribeirão Preto, São Paulo, Brazil, from 1977 to 1981, indicated that 61.9 % of nests were re-used by succeeding generations. Re-use by one generation was more frequent than by two generations, and re-use by a third was observed only once. Nests were re-used by one or several females. Single females were more frequently in the first re-use. In these cases nest re-use did not differ essentially from the solitary foundation of a new nest, except for the adoption of a pre-existing nest without excavation. In multifemale nests, analysis of relative age (wing wear), ovarian and spermathecal conditions of associated females and the content of nests at excavation indicated that the social pattern in such colonies is communal. There is some evidence that the associated females are relatives. The chalcidoid waspLeucospis was the principal nest parasite, and ants of the genusCrematogaster were nest predators. In multifemale nests, the rate of parasitism was significantly lower than in solitary nests, indicating that nest-sharing resulted in improved nest defense. On the other hand, the absence of predation on immatures of the first generation of M.commbae in multifemale nests suggests that such nests are also more resistant to attack by predators.     

Seabird nest counts: a test of monitoring metrics using Red-tailed Tropicbirds

ABSTRACT.   Counts of nesting birds are often used to monitor the abundance of breeding pairs at colonies. Mean incubation counts (MICs) are counts of nests with eggs at intervals that correspond to the mean incubation period of a species. The sum of all counts during the nesting season (MIC_total) and the highest single count during the season (MIC_max) are metrics that can be generated from this method. However, the utility of these metrics as measures of the number of breeding pairs has not been well tested. We used two approaches to evaluate the bias and precision of MIC metrics for quantifying annual variation in the number of breeding Red-tailed Tropicbirds ( Phaethon rubricauda ) nesting on two islands in the Papahānaumokuākea Marine National Monument in the northwest Hawaiian Islands. First, we used data from nest plots with individually marked birds to generate simulated MIC metrics that we compared to the known number of nesting individuals. The MIC_total overestimated the number of pairs by about 5%, whereas the MIC_max underestimated the number of pairs by about 60%. However, both metrics exhibited similar precision. Second, we used a 12-yr time series of island-wide MICs to compare estimates of temporal trend and annual variation using the MIC_max and MIC_total. The 95% confidence intervals for the trend estimates were overlapping and the residual standard errors for the two metrics were similar. Our results suggest that both metrics offered similar precision for indices of breeding pairs of Red-tailed Tropicbirds, but that MIC_total was more accurate.     

Nest sites,nest depredation,and productivity of avian broods in a primeval temperate forest: do the generalisations hold?

Data on nest success and brood productivity of three ground-nesting, three canopy-nesting and four hole-nesting (non-excavator) passerines were gathered in a primeval lowland temperate forest (Bialowieza National Park, E Poland). Natural holes were superabundant and the birds had to cope with a heavy pressure of a diverse assemblage of nest predators. We tested whether in such conditions nesting in holes is more productive, and whether nesting on the ground is most risky, as expected from some earlier generalisations. The nesting success varied significantly across the nest types. As predicted, the success of hole-nesters (51–74%) and their brood productivity were the highest. Contrary to expectations, the ground-nesters (27–40%) did not breed less successfully than the canopy-nesters (22–33%). Nest predators, responsible for 64–94% of nest losses in individual species, were the major cause of the differences among nest types. The Bialowieza results confirm the long-held view that holes tend to be the safest breeding places, but lend no support for the idea that nesting on the ground is more dangerous than in tree crowns.     

Application of the biogenetic law to behavioral ontogeny: a test using nest architecture in paper wasps

General principles derived from studies of morphological ontogeny are useful in ethology. Behavioral ontogeny may be interpreted from an holistic view in which a series of behaviors is treated as an ontogeny toward a larger, complex, behavioral product. If the component behaviors are defined broadly, many taxa may be compared to find general principles that are not evident when behaviors are dissected to their smallest recognizable units. Flow charts can illustrate such general ontogenetic sequences in a manner that shows what sorts of modifications have evolved from the general pattern. Certain changes may illustrate forms of ontogenetic evolution that are well known for morphological development, such as addition or embellishment of terminal ontogenetic steps, or compression of ontogeny by acceleration or deletion of early steps. The major modifications in nest construction behavior of 28 genera of paper wasps are presented to test the predictions of the biogenetic rule with respect to character polarity. Cladistic analyses of separate morphological and behavioral data sets show that polarity is accurately inferred with respect to the five major patterns of nest construction in paper wasps.     

To nest communally or not to nest communally: a review of rodent communal nesting and nursing

Communal nesting, the sharing of parental responsibilities between multiple individuals in a nest, is common in many rodents. Upon first glance, this behaviour seems to be selectively disadvantageous. Communal care not only involves energetic costs, but may also be subject to cheating behaviour. Despite abundant literature, many questions remain regarding advantages gained by females that form nesting groups. I discuss the communal nesting of eusocial, singular and plural breeding rodents. I first clarify the distinction between communal nesting and thermoregulatory huddling. I then review two major groups of hypotheses ('ecological constraints' and 'benefits of philopatry') that are used to explain the occurrence of communal nesting in rodents. Most likely, these hypotheses are not mutually exclusive. Regardless of the main selective pressure(s) acting on communal nesting, the indirect components of inclusive fitness that result from nest sharing most likely influence the formation and maintenance of communal nests. Communal nesting and nursing (the sharing of milk with nonoffspring) are under different selective regimes and thus, must be evaluated separately. I review adaptive and nonadaptive hypotheses for rodent communal nursing. I argue that communal nursing may not be adaptive as mothers may be forced to share milk with nonoffspring in large communal nests (i.e. communal nursing may be a cost associated with communal nesting). In conclusion, I propose directions for future study that may improve our understanding of communal nesting and nursing in the wild. Copyright 2000 The Association for the Study of Animal Behaviour.     

Nest preference of laying hens (Gallus gallus domesticus) and their motivation to exert themselves to gain nest access

In connection with the development of a test method for the attractiveness and appropriateness of nests for laying hens, we carried out an investigation by using a preference test and motivation measuring with the help of push doors. Hens were offered two different nest sites either consisting of a tray filled with wood shavings (litter tray) or a wooden nest box plus wood shavings (nest box). Hens were individually housed in pens (2.0 m × 2.0 m) and had free access to the nest sites until they laid their 15th egg. From that day the hens had to overcome a push door to reach the nest sites. Resistance for entrance was also increased stepwise at the door leading to the hens’ nest. The experiment ended when a hen stopped to lay in her usual nest site for four consecutive days (postexperimental period). The behaviour during the last hour before oviposition was video taped at a level of resistance of 3.5, 6.0, 7.5 and 10.0 N.The hens were categorized into nest and litter layers depending on nest choice. All but one hen pushed maximum resistances between 11.5 and 18.0 N with no differences between nest and litter layers. Behaviour did not significantly change with increasing levels of resistance, but there were significant differences between nest and litter layers. Nest layers spent more time nesting than litter layers while the latter showed a strong tendency to more exploring behaviour. For litter layers, more entries through the push door leading to their nest site and more unsuccessful pushes were detected than for nest layers. According to our results, two types of layers could be distinguished whereas the two were equally motivated to access their nest site.     

Nest positioning by male Daito White‐eyes Zosterops japonicus daitoensis improves with age to reduce nest predation risk

Age‐related improvement in reproductive success is widely observed in birds, and the mechanisms by which productivity is enhanced have received considerable attention. However, little is known about how parental age affects the loss of eggs or nestlings despite the fact that age effects on nesting success are often reported. We examined parental age effects on reproductive success in relation to the avoidance of nest predation in an island subspecies of the Japanese White‐eye, the Daito White‐eye Zosterops japonicus daitoensis. Clutch size and annual number of breeding attempts did not differ between parental age classes. Reproductive success was affected only by male age through an increase in nesting success. Nest failure was attributed only to predation in this species and nest concealment and nest height were important nest characteristics promoting successful fledging. Older males built their nests in more concealed and higher positions than first‐year birds, regardless of vegetation status around the nest. Analysis of individual birds suggested that by shifting the nest to a safer position, male White‐eyes achieved higher nesting success than in the previous year. Of three hypotheses of age‐related improvement in reproductive success considered, our data favoured the hypothesis that as individuals grow older, their breeding competence improves.     

Nest size predicts the effect of food supplementation to magpie nestlings on their immunocompetence: an experimental test of nest size indicating parental ability

Post-mating sexually selected signals are expected to indicateparental quality. The good parent model assumes that expressionof the sexual character positively reflects parental ability,resulting in a potential link between the exaggeration of thecharacter and nestling-fitness traits. We tested this predictionin a population of a monogamous passerine, the magpie (Picapica), for which nest size is known to act as a post-matingsexually selected signal. We provided a food supplement to halfof the magpie nestlings in each nest, keeping the other halfas control nestlings. We found that food-supplemented nestlingsexperienced a significantly higher T-cell-mediated immune responseand a tendency to an increased condition index. In accordancewith the good parent model, we found that nest size was positivelyrelated to T-cell mediated immune response for control magpie,whereas this relationship was nonexistent in food-supplementednestlings. In addition, the difference in T-cell mediated immuneresponse between food-supplemented and control nestlings ofthe same nest was principally explained by nest size. Basedon our results, we discuss that magpie pairs with large nestsprovided their nestlings with higher quality food as comparedto pairs with smaller nests, nest size thereby being an indicatorof parental ability. To our knowledge, this is the first studyshowing a link between a post-mating sexually selected signaland nestling immunocompetence, a trait closely related to fitnessin birds.