Does nest predation pressure influence the energetic cost of nest guarding in a teleost fish?

The energetic costs of providing parental care are widely documented, but rarely do studies consider the role of environmental variation (e.g., predation pressure) in this context. Here, we tested if variation in nest predation pressure influenced the energetic costs of parental care in smallmouth bass (Micropterus dolomieu), a teleost fish species that provides lengthy paternal care. First, we documented that nest predation pressure varied among the six lakes studied and the relative predation pressure ranking was consistent across a three year period. We used a combination of traditional proximate body composition (PBC) analyses and electromyogram (EMG) telemetry to quantify activity costs of nesting fish across these populations. The traditional approach revealed declines in energy stores across the parental care period but showed no evidence of an increased energetic cost to parents from populations with higher nest predation pressure. Comparing the distribution of EMG data from the two extremes of predation pressure revealed that males from the site of highest predation spent more time at higher EMG levels relative to the parents from the lake of lowest predation pressure. Although not statistically significant, males from the site of highest predation pressure also spent 21?C24?% of their time burst swimming when guarding young offspring compared to 10?C11?% for males at the site of lowest predation pressure. These differences in overall activity, a large contributor to the energy use of fish, may translate into longer recovery times and decreased future reproductive opportunities.     

Monk parakeet invasion success: a role for nest thermoregulation and bactericidal potential of plant nest material?

Invasive species are a global threat to biodiversity, economy and human wellbeing. To mitigate these threats, identifying and halting the introduction of potentially invasive species is crucial. Although progress has been made in elucidating mechanisms underlying invasion success, the role of species behavioral strategies has only received scant attention. Here, we use the invasion of monk parakeets in Santa Catarina state, southern Brazil to study whether behavioral strategies such as nest thermoregulation and the ability to self-medicate against pathogens contribute to the establishment success of invading species. We relate data on monk parakeet reproductive success to ambient temperatures in- and outside nesting chambers and test the bactericidal potential of plants transported to the nest by breeding monk parakeets. Compared to breeding data from other invaded ranges and parts of the species’ native range, our results suggest both thermoregulation and the use of bactericidal plants could potentially influence monk parakeet reproductive success. Thermoregulation maintains stable temperatures of incubator chambers compared to large fluctuations (especially hotter extremes) outside the nest. At least one of the plants brought to the nest effectively inhibited growth of pathogenic bacteria. The union of these two factors could increase reproductive rates and may consequently aid the expansion of the species in new non-native environments.     

Seasonal habitat-dependent change in nest box occupation by Tengmalm’s owl associated with a corresponding change in nest predation

We investigated the nest-site settlement of the forest-dwelling Tengmalm’s owl (Aegolius funereus) in the temperate zone of Central Europe (Czech Republic) over a 14-year period. We analysed the effect of changes in nest-site suitability (expressed as the proportion of deciduous forest) within the immediate surroundings of the nest boxes (a buffer radius of 25 m) in relation to nest box occupancy, the mean standardized laying date (further the laying date), occurrence of nest predation, and breeding density. In line with the predictions of the site dependence model, we found a positive relationship between the laying date and the proportion of deciduous trees in the nest box surrounding. Further, we found the interactive effect of the laying date and the proportion of deciduous forest surrounding a nest box on the occurrence of breeding attempts predated by pine martens. A higher proportion of deciduous forest was found in the surroundings of predated than non-predated breeding attempts, and a steeper positive relationship between the laying date and the proportion of deciduous forest was found in the surroundings of non-predated than predated breeding attempts. The change in the owls’ habitat utilization can be explained by the process of tree leafing which makes the deciduous forest a less suitable habitat with high risk of nest predation before tree foliage and a more suitable habitat with low risk of nest predation after tree foliage. We conclude that our results are in agreement with the site dependence model, and that the degree of foliage of deciduous forest in the nest surrounding of Tengmalm’s owl is a key factor determining site suitability due to predation risk from pine martens in Central Europe.     

Prolactin and parental behavior in Adélie penguins: effects of absence from nest, incubation length, and nest failure

Adélie penguin (Pygoscelis adeliae) males and females, nesting in Antarctica, alternate attendance at the nest with absences of many days to forage at sea. We investigated the importance of tactile input from egg and chicks on prolactin levels by observing nest attendance patterns and obtaining blood samples (1) during the first nest exchange of the incubation stage, (2) from birds whose incubation period was artificially increased or decreased by about 10 days, and (3) from birds whose nests had failed. Prolactin levels in females after 8 to 11 days of absence from the breeding colony did not differ from those in incubating males and did not change after females resumed incubation. Moving eggs between nests resulted in nests in which chicks hatched after about 26, 36 (normal), or 46 days. Duration of incubation did not affect prolactin levels in the parents measured during incubation, at the pip stage, hatch stage, or early brood stage. Adults first left their chicks unguarded on about the same calendar date, regardless of chick age. However, chicks from long incubation nests averaged 8 days younger when they were left unguarded than chicks from control or short-incubation nests. In females, there was no effect of nest failure on prolactin levels. In males, prolactin levels were slightly lower after nest failure than in males tending nests. Testosterone was significantly higher in males after nest failure than in males still tending nests. Prolactin is elevated in Adélie penguins as part of the program of cyclical hormonal changes that accompany the lengthy reproductive season and is relatively independent of tactile input. Sustained prolactin secretion is probably required for the maintenance of parental behavior in offshore feeding species that must be absent from the nest for many days at a time.     

Nesting season,nest age,and disturbance,but not habitat characteristics,affect nest survival of Chinese grouse

Nest survival is a vital component of breeding success,and affects population dynamics,as the loss of nests is the main cause of reproductive failure in birds.To identify key factors for the conservation of Chinese grouse Tetrastes sewerzowi,we tested the effects of nest concealment,nest age,nesting season,and habitat edge on nest daily survival rate(DSR)of Chinese grouse using 54 nests found at Lianhuashan Nature Reserve,Gansu,China,2009-2012.Moreover,we controlled for the effect of research activity by testing the effect of nest checks on DSR.Overall,mammal predation caused 93%of nest failures.DSR was 0.986±0.0038 in the constant model and the probability of a nest with a full clutch of 6 eggs surviving the entire 40-day nesting period was 0.526±0.090.DSR decreased with nest age and nesting season(from 19 May to 3 July).Mammals instead of avian predators being responsible for most nest failures suggest that nest sites might be selected to avoid visual avian predators,but not olfactory mammalian predators,and the decreasing trend of DSR with nest age and nesting season could attribute to an additive exposure effect.Moreover,nest checks conducted by investigators significantly lowered nest DSR,especially during the late period of nesting season and for older nests.Mammalian predators might locate the nest site by following the investigator's odor.Based on our results,we suggest that the late incubation stage is a particularly vulnerable period for nest survival of Chinese grouse and those researchers should adjust their activities around nests to balance the need of acquiring accurate data and decreasing nest predation risk.     

Nest height, nest concealment, and predator type predict nest predation in superb fairy-wrens (Malurus?cyaneus)

Three factors and their interaction effects are increasingly recognized as important determinants of nest predation: nest concealment, nest height, and predator type. The risk of nest predation is predicted to vary across these variables because of nest detectability and accessibility. In general, however, few studies examine how these three variables interact in relation to nest predation, focusing instead on either nest concealment or nest height (whereby predator identity is usually not known). In this study, we examine the role of nest concealment and nest height for nest survival using both artificial and natural nests in the superb fairy-wren (Malurus cyaneus). We indirectly identified potential predators through marks left on artificial eggs and footprints left on tracking tunnels. Predation level at artificial nests was lower than at natural nests, and this could be due to a failure of some nest predators to locate cryptic nests in the absence of cues provided by parental activity. Our results supported the prediction that exposed and concealed nests have different levels of nest predation, which can be explained by variation in predator type. Visual predators were only detected at exposed nests, and survival from visual predators was lower for high nests that were also exposed. However, olfactory predators were detected irrespective of nest height or nest concealment. Because rodents use olfaction to locate nests, this could explain the lack of association between nest concealment and predation outcome at low nests. In addition, rodent footmarks near nests were significantly associated with rodent tooth marks on eggs.     

Facultative nest patch shifts in response to nest predation risk in the Brewer’s sparrow: a “win-stay, lose-switch” strategy?

Facultative shifts in nesting habitat selection in response to perceived predation risk may allow animals to increase the survival probability of sessile offspring. Previous studies on this behavioral strategy have primarily focused on single attributes, such as the distance moved or changes in nesting substrate. However, nest site choice often encompasses multiple habitat elements at both the nest site and nest patch scales. We studied the within-season re-nesting strategy of a multi-brooded songbird, the Brewer’s sparrow (Spizella breweri), to determine whether pairs utilized a “win-stay, lose-switch” decision rule with respect to inter-nest distance, nest substrate and/or nest patch characteristics in response to previous nest fate. Pairs moved sequential nest sites slightly farther following nest predation versus success. When inter-nest distance was controlled, however, pairs changed nest patch attributes (shrub height, potential nest shrub density) associated with probability of nest predation to a greater extent following nest predation than success. The strategy appeared to be adaptive; daily nest survival probability for previously depredated pairs increased with greater Euclidian habitat distances between attempts, whereas previously successful pairs were more likely to fledge second attempts when nest sites were similar to those of previous attempts. Our results suggest that nesting birds can use prior information and within-season plasticity in response to nest predation to increase re-nesting success, which may be a critical behavioral strategy within complex nest predator environments. Re-nesting site selection strategies also appeared to integrate multiple habitat components and inter-nest distances. The consideration of such proximate, facultative responses to predation risk may clarify often unexplained variation in habitat preferences and requirements.     

Providing nest boxes for hole-nesting birds – Does habitat matter?

Nest boxes are a popular management tool to increase nest site availability for hole-nesting birds, but biological consequences of this technique in different habitats are poorly studied. In our study area in southwestern Estonia, nest boxes for small passerines were set up in deciduous and coniferous woods. Great tits Parus major preferred the food-rich deciduous habitat for breeding, as judged by higher nest-box occupation, earlier egg-laying and larger clutches and eggs. However, in coniferous habitat more and heavier young fledged per nest, and the return rate of both fledglings and adults was higher. We propose two mutually non-exclusive explanations, both related to the maladaptive outcome of the provision of nest boxes: (i) in the preferred habitat, nest boxes caused a supra-optimal breeding density leading to an ecological trap; (ii) boxes drastically improved the non-preferred habitat, but birds were unable to exploit the breeding habitat fully. One should be careful in providing large numbers of artificial nest sites in preferred habitats. Sometimes it would be more preferable to improve less favourable habitats by removing critical constraints.     

Do female degus communally nest and nurse their pups?

We examined the nesting and nursing behavior of females of the caviomorph rodent Octodon degus. We recorded the behavior of two, three-female groups of lactating degus kept in captivity and compared it with that of singly housed lactating females. Grouped females spontaneously nested communally. Five of six lactating females had non-offspring pups hanging from their teats, which suggests that some non-offspring nursing took place. Non-mothers increased their maternal behavior after the delivery of their own pups. Although time allocated to parental care by each communally nesting dam did not differ from that of solitary lactating females, young of communal litters spent less time alone and enjoyed more time cared for by a lactating female than young of single dams. Electronic Publication     

Do artificial nests reveal relative nest predation risk for real nests?

Present knowledge of the effects of nest predation on spatial distribution, habitat selection and community structure of birds is to a large extent based on results from experiments with artificial nests. Although nest predation risk is likely to differ between artificial and real nests, most previous studies of nest predation using artificial nests have been lacking a proper control. We investigated whether predation rates on artificial nests predicted those on real nests by simultaneously comparing the fate of real and artificial nests (containing quail Coturnix coturnix and plasticine eggs) in 92 territories of the northern wheatear Oenanthe oenanthe in 1996. We also investigated whether risk for artificial nests was related to relative average risk for real nests in these territories (based on data collected two years before and two years after the experiment). Nest predation on artificial nests did predict relative predation risk for real nests only when quail egg depredation was used as the criterion for artificial nest predation. Despite plasticine egg depredation being the most common type of predation it was not associated with predation risk for real nests. Small mice and vole species dominated among cases with only plasticine egg depredation, while predatory mammals and snakes destroyed most quail eggs in artificial nests and most eggs in real wheatear nests. The results suggest that artificial nests may only predict the risk for real nests when the nest predator species are similar among the two types of nest. Furthermore, our data suggest that small mice and vole species rarely depredate nests of mid-sized passerine birds . Our results cast doubt on many previous conclusions based on experiments with artificial nests, since predation risk for such nests is likely to be uncorrelated with risk for real nests due to nest-type-specific differences in nest preying species.     

Sex‐specific differences in Sand Martin Riparia riparia nest attentiveness

Capsule Nest attentiveness during the night is significantly lower in males but varies with the activities of the breeding cycle. Male nest attentiveness shows minima during the burrowing and egg‐laying phases, and also during the brooding of chicks in second or re‐nest broods.     

Do pinyon jays alter nest placement based on prior experience?

The role of prior experience in nest-site selection by a long-lived corvid, the pinyon jay, Gymnorhinus cyanocephalus, was investigated. The major sources of nest failure were loss to avian predators (Corvus corax and Corvus brachyrhynchos) and abandonment after cold and snowy spring weather. Cold weather favours exposed nesting because solar radiation reduces the energetic costs to nesting females and quickly melts snow in and around the nest. Predation favours cryptic nests. The relative height at which individual jays nested (an index of nest exposure) was compared to their previous nest height and to the fate of that nesting attempt. For the following reasons jays appear to associate nest exposure with the fate of a particular nesting attempt: (1) after nesting in exposed sites, subsequent nests were 27·3% lower (more concealed) in the nest tree following predation, but only 9·7% lower when predation did not occur; (2) concealed nest sites were avoided only after failure due to cold weather; and (3) nest placement following the successful fledging of young did not differ significantly from the previous nest placement. The frequency of nesting in exposed locations dropped from 80% to 55% after individuals suffered their third predatory experience when nesting in exposed locations. Experienced jays nested relatively low throughout the season, which enhances concealment, but nested farther out from the trunk early in the season, which reduces incubation costs. The use of prior experience in nest-site selection is adaptive because sites can include properties associated with past success and exclude those associated with past failure.     

Does nest box use reduce the fitness of a tree-cavity dependent mammal?

Nest boxes are frequently used in conservation programs for tree-cavity dependent wildlife. There is growing concern that the poor insulation properties of nest boxes may produce an ecological trap, because species may require microclimates less extreme or less variable than those experienced inside nest boxes. I investigated the fitness consequences of nest box use in a non-flying mammal. Fifty-two of 104 squirrel gliders (Petaurus norfolcensis) trapped over a 3-year period used nest boxes. Population modelling of the capture data revealed that the probability of apparent survival increased with increasing nest box use. There was no difference in breeding frequency between females that used or did not use nest boxes. There was no evidence that offspring development was hindered within nest boxes. These findings may arise because: (1) gliders could access tree hollows during extreme temperatures, (2) ambient temperatures were mild during the study, (3) gliders construct leaf nests which insulate against low temperatures in winter, and (4) gliders breed between autumn and spring when temperatures are relatively benign. The estimate of annual survival of animals using nest boxes (0.60), was equivalent to estimates at locations where squirrel gliders were either reliant on nest boxes (0.54) or on tree cavities (0.55) for shelter. Studies such as this need to be conducted on a range of species across a range of locations to better understand the influence of nest box use on non-flying mammals.     

“Wall-papering” and elaborate nest architecture in the ponerine antHarpegnathos saltator

Summary Excavation of 18 nests ofHarpegnathos saltator from southern India revealed an unusually complex architecture for a ponerine ant. The inhabited chambers are not deep in the ground. The uppermost chamber is protected by a thick vaulted roof, on the outside of which is an intervening space serving as isolation from the surrounding soil. In large colonies, the vaulted roof is extended into a shell which encloses several superimposed chambers. Little openings, which may be encircled by moulded flanges, occur in the upper region of the shell. The inside of the chambers is partly or completely lined with strips of empty cocoons. A refuse chamber is always found deeper than the inhabited chambers; live dipteran larvae (family Milichiidae) are typically present. These elaborate nests represent a large energetic investment, and we speculate therefore that nest emigration is unlikely in this species. Consequently, colony fission may never occur, unlike other ants where gamergates reproduce.     

Can individual heterogeneity influence self-organised patterns in the termite nest construction model?

We present investigations on the influence of individual heterogeneity on self-organised patterns in the termite nest construction model. The presented results extend the original model (Bruinsma 1979; Deneubourg 1977) from theoretical biology which has served as foundation and inspiration for computational optimisation approaches. Our findings have implications for the handling of heterogeneities inherent to physical sensing devices as well as indicate the potential of intentionally endowing software agents or their hardware embodiments (robots, sensor nodes, etc.) with a degree of individuality. We show that increasing heterogeneity is equivalent to changing the values of certain global parameters.