The influence of parental behavior on vulnerability to nest predation in tropical thrushes of an Andean cloud forest

The Skutch hypothesis predicts that parental activity around the nest may attract the attention of predators and thus, in the tropics where predation pressure may be high, selection favors reduced parental activity. This hypothesis has been questioned by studies demonstrating that parents can decrease the risk of nest predation through nest defense. The link between parental activity and predation risk may be further confounded by nest site characteristics. We examined the effects of parental behavior and nest site on clutch survival in two sympatric tropical thrushes (Myadestes ralloides and Turdus leucops). We compared survival rates of clutches in three treatments: 1) natural nests at the incubation stage, 2) unattended nests (un‐manipulated nests of the same species, with clutches unattended by parents), and 3) exposed clutches (eggs exposed in unconcealed positions, unprotected by the nest). Parental activity had a positive effect on clutch survival, which was revealed by significantly higher survival rate of clutches in attended nests compared to unattended nests. The effect of nest site was less clear: clutches in unattended natural nests survived better than clutches in exposed sites selected by humans, but results were insignificant. We propose that parent birds can exclude a group of opportunistic predators, that are able to destroy unattended clutches. Nest site characteristics may be less important in determining clutch survival in the tropics, where predator guilds are more diverse, making completely safe sites difficult to find. Our results challenge Skutch's hypothesis and point to the need for more data from tropical latitudes.     

Experimental heating reveals nest temperature affects nestling condition in tree swallows (Tachycineta bicolor)

Investment in one life-history stage can have delayed effects on subsequent life-history stages within a single reproductive bout. We experimentally heated tree swallow (Tachycineta bicolor) nests during incubation to test for effects on parental and nestling conditions. Females incubating in heated boxes maintained higher body condition and fed nestlings at higher rates. We cross-fostered nestlings and found that young nestlings (4-7 days old) incubated in heated nests had higher body condition and body mass, regardless of treatment status of their rearing parent. However, older nestlings which were fed by heated females maintained higher condition and body mass regardless of treatment status of their incubating parent. These results indicate that investment in one life-history stage can have multiple pathways of carry-over effects on future life-history stages.     

Nest Crypsis, Reproductive Value of a Clutch and Escape Decisions in Incubating Female Mallards Anas platyrhynchos

In cryptically coloured birds, remaining on the nest despite predator approach (risk‐taking) may decrease the likelihood that the nest will be detected and current reproductive attempt lost. By contrast, flushing may immediately reveal the nest location to the predator. Escape decisions of incubating parents should therefore be optimized based on the risk‐to‐parent/cost of escape equilibrium. Animal prey may assess predation risk depending on a variety of cues, including the camouflage that vegetation provides against the predator. We examined interactive effects of nest crypsis and the current reproductive value of a clutch on flushing distances in incubating mallards (Anas platyrhynchos) approached by a human. Our results were consistent with predictions of parental investment theory: flushing distances were inversely correlated with measures of the reproductive value of the current clutch, namely with clutch size, stage of incubation and mean egg volume. Independently of a reproductive value of a clutch, nest concealment explained a significant portion of the variation in flushing distance among females; individual females tended to increase/decrease flushing distances according to change in nest cover. The results further suggest that vegetation concealment greatly influenced the risk of nest detection by local predators, suggesting that vegetation may act as a protective cover for incubating female. A female's ability to delay flushes according to the actual vegetation cover might thus be viewed as an antipredator strategy that reduces premature nest advertising to visually oriented predators. We argue, however, that shorter flying distances from densely covered sites might be maladaptive in areas where a predator's ability to detect incubating female does not rely on visual cues of nests.     

Do energetic demands constrain incubation scheduling in a biparental species?

The high energetic demands of incubation in birds may be animportant ecological factor limiting the evolution of life-historytraits, such as clutch size. In biparental species, however,the demands of incubation may not be a major constraint becausethere may always be sufficient feeding time available for theoff-duty bird to regain energy used during an incubation bout.We investigated whether the energetic demands of incubationconstrain optimum incubation bout length in a biparental incubatorby decreasing the energetic demands of incubation. We put aninsulated cup around the lining of semipalmated sandpiper nestsso that the rate of cooling of eggs was reduced by 21%. Semipalmatedsandpipers responded by increasing their mean incubation boutlength of around 11.1 h by about 10%. Bout lengths in unmanipulatednatural nests became longer as hatch approached (incubationstage), and this was independent of weather. Bout lengths mayhave decreased with increasing rainfall and were independentof time of day. The results suggest that bout length in semipalmatedsandpipers is constrained by their cumulative energetic expenditureduring an incubation bout, and this is determined partly bythe high costs of steady-state incubation. The results alsosuggest that the incubating bird determines the bout lengthrather than the returning bird. Semipalmated sandpipersmay havemaximized incubation bout length to minimize changeovers duringincubation because these probably increasepredation risk. Selectionto minimize the frequency of changeover may then be a factorcontributing to the evolution ofbiparental care and life-historytraits in semipalmated sandpipers.     

Plasticity in incubation behavior and shading by king rails Rallus elegans in response to temperature

King rails experience a wide range of temperatures during the course of the breeding season throughout their rapidly contracting geographic range. Incubating parent birds are adapted to keep their eggs within a temperature range appropriate for embryo development, but king rail clutches are at risk of exceeding lethal temperatures in the latter half of the nesting season. We investigated whether behavioral plasticity during incubation enables parents to maintain clutch temperature within tolerable limits for embryo development. Video revealed that king rail parents interrupted incubation to stand above and shade their eggs. We tested the hypothesis that the onset of shading was a direct response to ambient temperature (adaptive plasticity). We monitored clutch temperature directly by experimentally adding into clutches a model egg embedded with a programmable iButton. We measured ambient temperature at the nest site simultaneously. Parents spent proportionately more time shading and less time incubating their eggs at higher ambient temperatures. Shading may primarily function in cooling the parent. The frequency and duration of shading bouts were significantly greater at higher ambient temperatures. Parents also took more frequent but shorter recesses in hotter conditions. Diurnal recesses exposed eggs to direct sunlight, and the highest clutch temperatures were recorded under these conditions. Complete hatching failure in at least one nest was attributable to high clutch temperature for an extended period. Because mean ambient temperature increases throughout the breeding season, we investigated seasonal patterns in onset of incubation and its effect on hatching rate. Later in the season, parents tended to initiate incubation earlier, and hatching asynchrony increased significantly. Together these results suggest that breeding king rails may be constrained in their ability to cope with sustained high temperatures should seasonal averages continue to rise as predicted.     

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.     

Buildings promote higher incubation temperatures and reduce nest attentiveness in a Neotropical thrush

Incubation is an energetically costly parental task of breeding birds. Incubating parents respond to environmental variation and nest‐site features to adjust the balance between the time spent incubating (i.e. nest attentiveness) and foraging to supply their own needs. Non‐natural nesting substrates such as human buildings impose new environmental contexts that may affect time allocation of incubating birds but this topic remains little studied. Here, we tested whether nesting substrate type (buildings vs. trees) affects the temperature inside the incubation chamber (hereafter ‘nest temperature’) in the Pale‐breasted Thrush Turdus leucomelas, either during ‘day’ (with incubation recesses) or ‘night’ periods (representing uninterrupted female presence at the nest). We also tested whether nesting substrate type affects the incubation time budget using air temperature and the day of the incubation cycle as covariates. Nest temperature, when controlled for microhabitat temperature, was higher at night and in nests in buildings but did not differ between daytime and night for nests in buildings, indicating that buildings partially compensate for incubation recesses by females with regard to nest temperature stability. Females from nests placed in buildings exhibited lower nest attentiveness (the overall percentage of time spent incubating) and had longer bouts off the nest. Higher air temperatures were significantly correlated with shorter bouts on the nest and longer bouts off the nest, but without affecting nest attentiveness. We suggest that the longer bouts off the nest taken by females of nests in buildings is a consequence of higher nest temperatures promoted by man‐made structures around these nests. Use of buildings as nesting substrate may therefore increase parental fitness due to a relaxed incubation budget, and potentially drive the evolution of incubation behaviour in certain urban bird populations.     

Parental behaviour in the Lapwing Vanellus vanellus

Parental behaviour of monogamous and polygynous Lapwings was studied during incubation and brood care. Both parents attended the nest in 86% of monogamous pairs ( n = 29 pairs). In 14% of pairs, only the male parent continued incubation until the eggs hatched, whereas the female deserted the clutch before or at the end of incubation. There was a clear division of parental roles during incubation. Females spent more time incubating (64% of time) than their mates (27%), whereas males spent more time defending the nest (3%) than females (>1%). Time spent incubating did not differ between monogamous and polygynous males. However, polygynous females spent more time incubating (primary females: 95%; secondary females: 97%) than monogamous females. Biparental care was the most common pattern of post-hatching care, although in some broods either the male or the female parent deserted before the chicks fledged. Division of sex roles was less pronounced in brood care than during incubation. Females spent more time brooding (21%) than males (3%), and females attended their chicks more closely than males. Nevertheless, males and females spent similar amounts of time defending the brood from predators and conspecifics. We suggest that the apparent division of parental roles may be explained by sexual selection, i.e. the remating opportunities for male Lapwings might be reduced if they increase their share in incubation. However, the different efficiency of care provision, for example in ability to defend offspring, may also influence the roles of the sexes in parental care.     

The bright incubate at night: sexual dichromatism and adaptive incubation division in an open-nesting shorebird

Ornamentation of parents poses a high risk for offspring because it reduces cryptic nest defence. Over a century ago, Wallace proposed that sexual dichromatism enhances crypsis of open-nesting females although subsequent studies found that dichromatism per se is not necessarily adaptive. We tested whether reduced female ornamentation in a sexually dichromatic species reduces the risk of clutch depredation and leads to adaptive parental roles in the red-capped plover Charadrius ruficapillus, a species with biparental incubation. Males had significantly brighter and redder head coloration than females. During daytime, when visually foraging predators are active, colour-matched model males incurred a higher risk of clutch depredation than females, whereas at night there was no difference in depredation risk between sexes. In turn, red-capped plovers maintained a strongly diurnal/nocturnal division of parental care during incubation, with males attending the nest largely at night when visual predators were inactive and females incubating during the day. We found support for Wallace''s conclusion that reduced female ornamentation provides a selective advantage when reproductive success is threatened by visually foraging predators. We conclude that predators may alter their prey''s parental care patterns and therefore may affect parental cooperation during care.     

Why do Both Parents Incubate in the Kentish Plover?

Incubation by both parents is a common parental behaviour in many avian species. Biparental incubation is expected if the survival prospects of offspring are greatly raised by shared care, relative to the costs incurred by each parent. We investigated this proposition in the Kentish plover Charadrius alexandrinus, in which both parents incubate the clutch, but one parent (either the male or the female) usually deserts after hatching of the eggs. We carried out a mate‐removal and food supplementation experiment to reveal both the role of the sexes and food abundance in maintaining biparental incubation by removing either the male or the female from the nest for a short period of time. In some nests we provided supplementary food for the parent that remained at the nest to reduce the costs of incubation, whereas other nests were left unsupplemented. Although males spent more time on incubation after their mate had been removed, females’ incubation did not change. Notwithstanding the increased male incubation, total nest attentiveness was lower at uniparental nests than at biparental controls. However, incubation behaviour was not influenced by food supplementation. We conclude that offspring desertion during incubation is apparently costly in the Kentish plover, and this cost cannot be ameliorated with supplementary food.     

Nest temperature, incubation period, and investment decisions of incubating wood ducks Aix sponsa

Incubating birds must balance their energetic demands with the time needed to provide care to developing embryos. Reduced care by incubating parents can result in longer incubation periods that increase predation risk and potentially influence neonate phenotype. We measured nest temperature, incubation period, and body mass dynamics of female wood ducks Aix sponsa , and used an information-theoretic approach to investigate effects of several explanatory variables on incubation period and thermal characteristics of nests. A model that included clutch size and standard deviation of nest temperature best explained the variation in incubation period. Parameter estimates indicated that incubation period increased with increases in clutch size and standard deviation of nest temperature. Next, we examined relationships between maternal effects and the standard deviation of the nest temperature. The best fitting model included initiation date of incubation. There was little support for including early incubation body mass of females, incubation constancy, and percent change in female body mass in the model. The parameter estimate showed that standard deviation of nest temperature declined as initiation date of incubation advanced. Female body mass at the start of incubation was not related to structural size suggesting that heavy females were in better physical condition than were light females. Heavy females nested earlier and lost more body mass during incubation than light females, but heavy females did not reduce variation in nest temperature to decrease the incubation period. The fact that early nesting females in good physical condition did not shorten incubation periods by keeping nest temperatures less variable could have been due to either energetic limitations or restraints. Experimental manipulations of incubation costs will be needed to distinguish between these hypotheses.     

Habitat-specific clutch size and cost of incubation in eiders reconsidered

The energetic incubation constraint hypothesis (EICH) for clutch size states that birds breeding in poor habitat may free up resources for future reproduction by laying a smaller clutch. The eider (Somateria mollissima) is considered a candidate for supporting this hypothesis. Clutch size is smaller in exposed nests, presumably because of faster heat loss and higher incubation cost, and, hence, smaller optimal clutch size. However, an alternative explanation is partial predation: the first egg(s) are left unattended and vulnerable to predation, which may disproportionately affect exposed nests, so clutch size may be underestimated. We experimentally investigated whether predation on first-laid eggs in eiders depends on nest cover. We then re-evaluated how nesting habitat affects clutch size and incubation costs based on long-term data, accounting for confounding effects between habitat and individual quality. We also experimentally assessed adult survival costs of nesting in sheltered nests. The risk of egg predation in experimental nests decreased with cover. Confounding between individual and habitat quality is unlikely, as clutch size was also smaller in open nests within individuals, and early and late breeders had similar nest cover characteristics. A trade-off between clutch and female safety may explain nest cover variation, as the risk of female capture by us, mimicking predation on adults, increased with nest cover. Nest habitat had no effect on female hatching weight or weight loss, while lower temperature during incubation had an unanticipated positive relationship with hatching weight. There were no indications of elevated costs of incubating larger clutches, while clutch size and colony size were positively correlated, a pattern not predicted by the ‘energetic incubation constraint’ hypothesis. Differential partial clutch predation thus offers the more parsimonious explanation for clutch size variation among habitats in eiders, highlighting the need for caution when analysing fecundity and associated life-history parameters when habitat-specific rates of clutch predation occur.     

Clutch predation in great tinamous Tinamus major and implications for the evolution of egg color

Egg camouflage has been found to reduce predation in several ground‐nesting species. Therefore, the evolution of eggs that lack camouflage in ground nesting birds is puzzling. Even though clutch predation in the tropics is high, tinamous are the only tropical ground‐nesting birds that do not build a nest and do not lay cryptic eggs. I studied predation of great tinamou clutches in a lowland tropical forest and found that risk of predation was higher during incubation when the eggs are covered by the parent, than during laying when they are exposed, suggesting that predators primarily use cues from the incubating males to locate the clutch and not cues from the eggs. Clutch size had no effect on predation rate, even though larger clutches are more conspicuous to a human observer. Predation by visual cues is likely reduced during incubation by the camouflaged plumage and high nest attendance of males. If most predators use cues from the incubating male and not the eggs to locate clutches, then conspicuous egg color may have evolved in great tinamous as an intra‐specific signal. I evaluate hypotheses that may explain the maintenance of conspicuous egg color in tinamous.     

Body condition and retaliation in the parental effort decisions of incubating great frigatebirds (Fregata minor)

Decisions about parental effort have the potential to be affectedby an individual's body condition and, among species with biparentalcare, by the level of effort made by one's mate. Previous studies,primarily of short-lived species, have found that a reductionin the parental effort of one pair member typically leads toa compensatory increase by the mate. However, long-lived specieswith short-term pair bonds might be expected to retaliate, ratherthan compensate, for a reduction in a mate's effort. I studiedthe factors affecting parental effort decisions during incubationby the great frigatebird, a long-lived seabird that forms newpair bonds for each breeding attempt. During incubation, malesand females took turns incubating and foraging. Individualslost mass during an incubation shift and regained this massduring the subsequent foraging bout. If an individual was lefton the nest for a long period of time while its mate was foraging,it subsequently went on a long foraging trip after being relievedby its mate, despite the fact that longer shifts were likelyto lead to nest failure. This relationship between incubationshift length and duration of subsequent foraging excursion could be due to a need to regain body condition after a longfast, or it could reflect a retaliatory response to the mate'sprolonged absence. To test these alternatives, I conducteda food supplementation experiment. Individuals engaged in along incubation shift were assigned to a control group or toa treatment group that was fed until the end of that particularincubation shift. Overall, fed birds returned from the subsequentforaging trip sooner than control birds, demonstrating thatthe relationship between incubation shift duration and foragingtrip duration is due primarily to a need to increase body mass,rather than being a retaliatory response to a mate's low levelof parental effort. However, males and females differed in theextent of their responses to the experimental treatment, indicatingthat males may also exhibit some degree of retaliation.     

Influence of incubation recess patterns on incubation period and hatchling traits in wood ducks Aix sponsa

Parental effects are influential sources of phenotypic variation in offspring. Incubation temperature in birds, which is largely driven by parental behavior and physiology, affects a suite of phenotypic traits in offspring including growth, immune function, stress endocrinology, and sex ratios. The importance of average incubation temperature on offspring phenotype has recently been described in birds, but parental incubation behaviors like the duration and frequency of recesses from the nest can be variable. There are few studies describing how or if thermal variation as a result of variable incubation affects offspring phenotype. We incubated wood duck Aix sponsa eggs under three different incubation regimes, based on patterns that occur in nature, which varied in off‐bout duration and/or temperature. We measured incubation period, morphometrics at hatching, and monitored growth and body condition for nine days post hatch. When average incubation temperature was allowed to drop from 35.9°C to 35.5°C as a result of doubled off‐bout duration, we found a significant 2 d extension in incubation period, but no effects on duckling hatch mass, or growth and body condition up to nine days post hatch. However, when average incubation temperatures were equivalent (35.9°C), doubling the duration of the simulated off‐bouts did not influence incubation period or any post hatch parameters. Our results suggest that if incubating parents can maintain favorable thermal environments in the nest via altered behavior (e.g. manipulating nest insulation) and/or physiology (e.g. heat production), parents may be able to avoid the costs of longer incubation periods resulting from increased off‐bout duration.     

Behavioral responses of nesting female dark‐eyed juncos Junco hyemalis to hetero‐ and conspecific passerine preen oils

Several studies have suggested a greater role for olfactory cues in avian social interactions than previously recognized, but few have explicitly investigated the effect of odor on parental behavior. We present results from a preliminary study in which we applied hetero‐ and conspecific preen gland secretions, which are known to contain volatile compounds, to the nests and eggs of incubating female dark‐eyed juncos Junco hyemalis. The responses to these two conditions were compared to the responses of females whose nests were treated with their own preen oil as a control condition, and to females whose nests were treated with the vehicle only. We found that females significantly reduced incubation bout length, a form of parental care, in response to alien secretions, more so if they came from a heterospecific than a conspecific. Females did not reduce incubation bout length in response to their own preen oil or to a vehicle‐only control. These results suggest that odors in the nest may influence avian parental care. However, the behavioral change was only temporary and had no effect on later hatching success. In our study population, brood parasitism by brown‐headed cowbirds is common, but resulting nest abandonment is rare; juncos are frequently able to successfully breed even with cowbird nestlings in their nests. Thus, we suggest that more extreme behavioral responses to alien odor, such as nest abandonment or egg ejection, may not be adaptive and should not be expected.     

How avian incubation behaviour influences egg surface temperatures: relationships with egg position,development and clutch size

While understanding heat exchange between incubating adults and their eggs is central to the study of avian incubation energetics, current theory based on thermal measurements from dummy eggs reveals little about the mechanisms of this heat exchange or behavioural implications for the incubating bird. For example, we know little about how birds distribute their eggs based on temperature differences among egg positions within the nest cup. We studied the great tit Parus major, a species with a large clutch size, to investigate surface cooling rates of individual eggs within the nest cup across a range of ambient temperatures in a field situation. Using state‐of‐the‐art portable infrared imaging and digital photography we tested for associations between egg surface temperature (and rate of cooling) and a combination of egg specific (mass, shape, laying order, position within clutch) and incubation specific (clutch size, ambient temperature, day of incubation) variables. Egg surface temperature and cooling rates were related to the position of the eggs within the nest cup, with outer eggs being initially colder and cooling quicker than central eggs. Between foraging bouts, females moved outer eggs significantly more than centrally positioned eggs. Our results demonstrate that females are capable of responding to individual egg temperature by moving eggs around the nest cup, and that the energy cost to the female may increase as incubation proceeds. In addition, our results showing that smaller clutches experience lower initial incubation temperatures and cool quicker than larger clutches warrant further attention for optimal clutch size theory and studies of energetic constraints during incubation. Finally, researchers using dummy eggs to record egg temperature have ignored important elements of contact‐incubation, namely the complexity of how eggs cool and how females respond to these changes.     

Female great tits Parus major do not increase their daily energy expenditure when incubating enlarged clutches

Several studies have shown that enlargement of clutches during incubation reduces the long-term survival of parents. In line with these findings, studies on the energetic costs of nocturnal incubation show an increase in energy expenditure with clutch enlargement. Studies on daily energy expenditure during incubation (DEE_inc), however, do not consistently show such a negative effect of clutch enlargement. To determine whether differential survival results from a direct increase in energy costs or rather from costs associated with compensatory behaviour, we studied the DEE_inc (kJ day⁻¹), change in body mass and nest attendance behaviour of free-living female great tits Parus major that incubated either control or experimentally enlarged clutches. DEE_inc did not differ between the two treatment groups, but was negatively related to mean ambient temperature over the 24-h measuring period, and to the fraction of daytime females spent on the nest. Controlling for these two factors, females incubating enlarged clutches did not spend more energy per 24 h period than females incubating control clutches. Clutch enlargement also did not affect body mass of incubating females, or their nest attendance behaviour. Yet, in the enlarged group body mass change and nest attentiveness were negatively correlated, suggesting that females responded differently to the experimental treatment and thereby preventing us from finding an effect of clutch enlargement.     

Regulation of foraging trips and costs of incubation shifts in the Antarctic petrel (Thalassoica antarctica)

In species where incubation is shared by both parents, the mate'sability to fast on the nest may constrain the time availablefor foraging. The decision to return to the nest should thereforebe a compromise between an animal's own foraging success andits mate's ability to fast on the nest. To examine how the bodyconditions of incubating Antarctic petrels, Thalassoica antarctica,influence both the length of foraging trips and incubation shifts,we experimentally handicapped females by increasing their flightcosts during a foraging trip by adding lead weights to theirlegs. Handicapped females spent more time at sea and had lowerbody conditions at arrival to the colony than controls, and,moreover, females in poor body condition at arrival to the colonyspent generally more time at sea than those with higher bodycondition. The prolonged time period spent at sea by handicappedfemales was associated with higher desertion rates than amongcontrols. The time the incubating mates fasted increased withtheir body condition at arrival to the colony, suggesting thata high body condition of the incubating bird may reduce theprobability of nest desertion. Accordingly, our results suggestthat the time spent foraging is adjusted to the body conditionsof both the foraging and incubating mate.     

Off‐nest behaviour in a biparentally incubating shorebird varies with sex,time of day and weather

Biparental incubation is a form of cooperation between parents, but it is not conflict‐free because parents trade off incubation against other activities (e.g. self‐maintenance, mating opportunities). How parents resolve such conflict and achieve cooperation remains unknown. To understand better the potential for conflict, cooperation and the constraints on incubation behaviour, investigation of the parents' behaviour, both during incubation and when they are off incubation‐duty, is necessary. Using a combination of automated incubation‐monitoring and radiotelemetry we simultaneously investigated the behaviours of both parents in the biparentally incubating Semipalmated Sandpiper Calidris pusilla, a shorebird breeding under continuous daylight in the high Arctic. Here, we describe the off‐nest behaviour of 32 off‐duty parents from 17 nests. Off‐duty parents roamed on average 224 m from their nest, implying that direct communication with the incubating partner is unlikely. On average, off‐duty parents spent only 59% of their time feeding. Off‐nest distance and behaviour (like previously reported incubation behaviour) differed between the sexes, and varied with time and weather. Males roamed less far from the nest and spent less time feeding than did females. At night, parents stayed closer to the nest and tended to spend less time feeding than during the day. Further exploratory analyses revealed that the time spent feeding increased over the incubation period, and that at night, but not during the day, off‐duty parents spent more time feeding under relatively windy conditions. Hence, under energetically stressful conditions, parents may be forced to feed more. Our results suggest that parents are likely to conflict over the favourable feeding times, i.e. over when to incubate (within a day or incubation period). Our study also indicates that Semipalmated Sandpiper parents do not continuously keep track of each other to optimize incubation scheduling and, hence, that the off‐duty parent's decision to remain closer to the nest drives the length of incubation bouts.