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.     

Interactive effects of time and vegetation on reproduction of redshanks (Tringa totanus) breeding in Wadden Sea salt marshes

As shown for various species, nesting waders are non-randomly distributed on wetlands and preferentially select riparian nest-sites adjacent to limnic or marine waterbodies. Studying the redshank Tringa totanus, we tested the hypotheses that, in a coastal wader species which conceals its clutch in vegetation, predation and hatching success are affected by vegetation zonation, and that breeding in lower salt marsh areas has negative consequences for reproduction. We further predicted effects of timing of breeding and breeding experience/age of adults potentially reflected by egg biometrics both on nest-site selection and reproduction. Effects of vegetation, space, time and individual quality on hatching success of redshanks were studied in the German part of the Wadden Sea. Dominant plant species, vertical vegetation structure and nest concealment varied significantly between nests. Variation in nest concealment was relatively low: about 90% of clutches were classified as being well concealed. This variation was explainable by vegetation structure but not by vegetation composition at the nest-site, distance to shoreline, and time of clutch initiation. Vertical vegetation structure varied by dominant plant species but not by distance to shoreline and time of clutch initiation. Hatching success of clutches was low (10.6%) due to high predation (daily predation rate: 7.4%). Hatching success and duration of clutch survival were negatively and predation positively related to the date of clutch initiation. Furthermore, negative relationships were found between egg size and predation and duration of survival, respectively. We assume that concealed nests, early breeding and breeding experience diminish predation in salt marsh breeding redshanks. Thus, redshank reproduction appears to be affected by interactive effects of timing of breeding and vegetation facilitating early breeding. In contrast to open-nesting species, breeding in riparian habitats next to waterbodies may be disadvantageous for species breeding concealed in vegetation if these are covered by less structured vegetation.     

Aggressive neighbors and dense nesting: nest site choice and success in high-Arctic common eiders

Minimizing the risk of nest predation has led some bird species to exploit the nest defense behavior of other species. At Nasaruvaalik Island, Nunavut, Canada, some common eiders (Somateria mollissima borealis) nest within the boundaries of Arctic tern (Sterna paradisaea) colonies, while others nest elsewhere on the island, away from the terns. We tested the effects of location (within vs. outside the tern colonies), density of common eider nests, and annual variation on the nesting parameters of common eiders. Our results suggest that nesting in association with Arctic terns does not confer an obvious benefit to eiders. Such associative nesting of eiders and terns may be the result of overlapping habitat preferences between the two species, or a general scarcity of suitable nesting habitat for ground-nesting species in the high Arctic. However, eiders nesting in higher densities with other eiders had greater nest success and lower total clutch predation, indicating a positive correlation between nest density and success.     

Building multiple nests is associated with reduced breeding performance in a south temperate population of Grass Wrens Cistothorus platensis platensis

Grass Wrens Cistothorus platensis build two types of non-breeding nest structures: platforms and dummy nests. Platforms are rudimentary accumulations of grasses concealed between vegetation. Dummy and breeding nests are dome-shaped with a similar structural layer. We used a nest-removal experiment and observational data to evaluate several hypotheses regarding the adaptive significance of building multiple nests in a south temperate population of Grass Wrens. Building non-breeding nests was not a strategy of males to attract additional females, as most of these nests were built after pair formation and both sexes collaborated during building. Building non-breeding nests was not a post-pairing display as the presence of multiple nests did not increase female investment in the breeding attempt: clutch size and female provisioning to nestlings did not differ between experimental and control territories where no non-breeding nests were removed. Similarly, in non-manipulated territories, clutch size and female provisioning were not correlated with the number of non-breeding nests or with males’ nest-building effort. Contrary to this hypothesis, the number of non-breeding nests was associated with delayed clutch initiation and reduced hatching success. The presence of non-breeding nests did not reduce nest predation and brood parasitism, which did not differ between experimental and control territories. We did not detect differences in concealment between non-breeding and breeding nests, suggesting that non-breeding nests were not the result of abandonment before egg-laying to reduce subsequent nest predation. Dummy nests did not provide shelter; they were not used frequently for roosting over the breeding season and were not maintained during the non-breeding season. We suggest that building non-breeding nests may be an attempt by males to manipulate the decision of females to breed with a mate they might otherwise reject or to start reproduction earlier than optimal for the females.     

Strategies for Nest-Site Selection by King Eiders

ABSTRACT Nest site selection is a critical component of reproduction and has presumably evolved in relation to predation, local resources, and microclimate. We investigated nest-site choice by king eiders (Somateria spectabilis) on the coastal plain of northern Alaska, USA, 2003–2005. We hypothesized that nest-site selection is driven by predator avoidance and that a variety of strategies including concealment, seclusion, and conspecific or inter-specific nest defense might lead to improved nesting success. We systematically searched wetland basins for king eider nests and measured habitat and social variables at nests (n = 212) and random locations (n = 493). King eiders made use of both secluded and concealed breeding strategies; logistic regression models revealed that females selected nests close to water, on islands, and in areas with high willow (Salix spp.) cover but did not select sites near conspecific or glaucous gull (Larus hyperboreus) nests. The most effective nest-placement strategy may vary depending on density and types of nest predators; seclusion is likely a mammalian-predator avoidance tactic whereas concealment may provide protection from avian predators. We recommend that managers in northern Alaska attempt to maintain wetland basins with islands and complex shorelines to provide potential nest sites in the vicinity of water.     

Boldness and Stress Responsiveness as Drivers of Nest‐Site Selection in a Ground‐Nesting Bird

Nest‐site selection involves trade‐offs between the probability of nest discovery by egg predators, danger to the incubating parent from predators and provision of an appropriate microclimate for incubation, and all three components are potentially influenced by nest concealment and distance to habitat edge. Personality traits also affect habitat choice, and the trade‐off hypothesis suggests that variable stress‐coping strategies may evolve because individuals prioritize either productivity (proactive coping) or survival (reactive coping), both of which cannot be simultaneously maximized. Applying this hypothesis to understand nest‐site selection by female eider ducks (Somateria mollissima), we predicted that bold individuals with attenuated stress responsiveness should select concealed nests further away from the shore, thereby promoting clutch survival at the potential expense of reduced escape opportunities for themselves. In testing this prediction, we controlled for individual quality (female body condition and breeding experience) and verified that individual stress responses and nest‐site preferences were consistent by analysing their repeatability. Finally, we analysed how the viable proportion of the clutch was related to nest‐site and female characteristics. Our prediction was supported: bold females [short flight initiation distance (FID)] and those with lower handling‐induced body temperature were found in concealed nests, and bold females and those with lower handling‐induced corticosterone concentrations occupied nests farther from the shore. The viable proportion of the clutch peaked at intermediate proportional nest‐cover and increased linearly with increasing nest distance from the shore. Stress coping styles may thus be related to nest‐site selection, but their fitness consequences may be manifested indirectly through the nest‐site characteristics.     

Nest Predation Deviates from Nest Predator Abundance in an Ecologically Trapped Bird

In human-modified environments, ecological traps may result from a preference for low-quality habitat where survival or reproductive success is lower than in high-quality habitat. It has often been shown that low reproductive success for birds in preferred habitat types was due to higher nest predator abundance. However, between-habitat differences in nest predation may only weakly correlate with differences in nest predator abundance. An ecological trap is at work in a farmland bird (Lanius collurio) that recently expanded its breeding habitat into open areas in plantation forests. This passerine bird shows a strong preference for forest habitat, but it has a higher nest success in farmland. We tested whether higher abundance of nest predators in the preferred habitat or, alternatively, a decoupling of nest predator abundance and nest predation explained this observed pattern of maladaptive habitat selection. More than 90% of brood failures were attributed to nest predation. Nest predator abundance was more than 50% higher in farmland, but nest predation was 17% higher in forest. Differences between nest predation on actual shrike nests and on artificial nests suggested that parent shrikes may facilitate nest disclosure for predators in forest more than they do in farmland. The level of caution by parent shrikes when visiting their nest during a simulated nest predator intrusion was the same in the two habitats, but nest concealment was considerably lower in forest, which contributes to explaining the higher nest predation in this habitat. We conclude that a decoupling of nest predator abundance and nest predation may create ecological traps in human-modified environments.     

Effects of clutch sizes and incubation stage on nest desertion in the female Common Eider Somateria mollissima nesting in the high Arctic

In bird species, one of the trade-offs between reproduction and survival appears in the parental decision to desert the nest. Nest desertion is modulated by several factors including clutch size. However, the incubation stage at which predation occurs is also an important factor. In this study, we examined whether nest desertion was linked to initial clutch size, partial clutch predation (final clutch size) and the incubation stage at which it happened in a capital breeder: the female common eider (Somateria mollissima) nesting in the high Arctic. The study was performed in Kongsfjorden in 2002 on the western coast of the Svalbard Archipelago (78°55′N, 20°07′E). We observed that nest desertion was higher when the initial clutch size was small. Also, females deserted their nests more during the first third of incubation than later. Thus, as incubation proceeded, nest desertion was less likely to occur even after egg reduction. Our results pointed out that this parental decision in female eiders seemed to depend on initial clutch size and on the date into incubation of clutch reduction. Sophie Bourgeon and Francois Criscuolo contributed equally to the work     

Effects of down collection on incubation temperature, nesting behaviour and hatching success of common eiders (Somateria mollissima) in west Iceland

Incubating common eiders (Somateria mollissima) insulate their nests with down to maintain desirable heat and humidity for their eggs. Eiderdown has been collected by Icelandic farmers for centuries, and down is replaced by hay during collection. This study determined whether down collecting affected the female eiders or their hatching success. We compared the following variables between down and hay nests: incubation temperature in the nest, incubation constancy, recess frequency, recess duration, egg rotation and hatching success of the clutch. Temperature data loggers recorded nest temperatures from 3 June to 9 July 2006 in nests insulated with down (n = 12) and hay (n = 12). The mean incubation temperatures, 31.5 and 30.7°C, in down and hay nests, or the maximum and minimum temperatures, did not differ between nest types where hatching succeeded. Cooling rates in down, on average 0.34°C/min and hay nests 0.44°C/min, were similar during incubation recesses. Females left their nests 0–4 times every 24 h regardless of nest type, for a mean duration of 45 and 47.5 min in down and hay nests, respectively. The mean frequency of egg rotation, 13.9 and 15.3 times every 24 h, was similar between down and hay nests, respectively. Hatching success adjusted for clutch size was similar, 0.60 and 0.67 in down and hay nests. These findings indicate that nest down is not a critical factor for the incubating eider. Because of high effect sizes for cooling rate and hatching success, we hesitate to conclude that absolutely no effects exist. However, we conclude that delaying down collection until just before eggs hatch will minimize any possible effect of down collection on females.     

人工巢箱条件下的大山雀巢捕食

于2004—2008年在次生阔叶林中,采用悬挂巢箱的方法对大山雀的巢捕食作了研究。结果表明:不同年龄巢箱的被捕食率显著不同,新巢箱被捕食率最低,第2年被捕食率最高,第3年下降很大,第4年又略有上升。被捕食巢的窝卵数极显著的低于未被捕食巢的窝卵数。影响巢捕食的主要生境因子为巢箱高度和巢上盖度,其次为灌木的密度和高度。     

How avian nest site selection responds to predation risk: testing an 'adaptive peak hypothesis'

1. Nest predation limits avian fitness, so birds should favour nest sites that minimize predation risk. Nevertheless, preferred nest microhabitat features are often uncorrelated with apparent variation in predation rates. 2. This lack of congruence between theory-based expectation and empirical data may arise when birds already occupy 'adaptive peaks'. If birds nest exclusively in low-predation microhabitats, microhabitat and nest predation may no longer be correlated even though predation ultimately shaped microhabitat selection. 3. This 'adaptive peak hypothesis' was tested for a population of Yellow Warblers (Dendroica petechia) focusing on two nest microhabitat features: concealment and height. Experimental nests measured relative predation risk both within and outside the microhabitat range typically occupied by natural nests to examine whether nest site choices made by birds restricted our ability to detect microhabitat effects on predation. 4. Within the natural range (30-80% concealment, >75 cm height), microhabitat-predation relationships were weak and inconsistent, and similar for experimental and natural nests. Over an extended range, however, experimental predation rates were elevated in exposed sites (<30% concealed), indicating a concealment-related 'adaptive plateau'. 5. Clay egg bite data revealed a concealment effect on avian predators, and the abundance of one avian predator group correlated with nest concealment among years, suggesting these predators may cue birds to modulate nest concealment choices. 6. This study demonstrates how avian responses to predation pressure can obscure the adaptive significance of nest site selection, so predation influences may be more important than apparent from published data.     

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.     

The influence of nest-site characteristics on the nesting success of the Karoo Prinia (Prinia maculosa)

Choice of nest site has important consequences for nest survival. We examined nest-site characteristics relative to nest success in Karoo Prinias breeding in coastal dwarf shrubland, where high nest predation is the main cause of nest failure. Initially, we compared nests that failed during the building, laying, incubation and nestling stages and those from which young were successfully raised, to test whether nests that survived to progressive stages in the nesting cycle differed in their nest-site characteristics. Subsequently, we compared the characteristics of successful nests with those of unsuccessful nests. The nest-site characteristics considered included nest height, nest-plant height, nest-plant species, distance from lateral foliage edge, nest concealment, nest-patch heterogeneity and vegetation cover at four different heights. We were unable to distinguish between the nest-site characteristics of nests that failed during the various stages of the nesting cycle. Concealment was the main nest-site characteristic that differentiated successful nests from unsuccessful nests, with successful nests being located in more concealed sites. The other variables that contributed to the discrimination between successful and unsuccessful nests by discriminant function analysis included nest-plant type and distance from edge, which are also directly related to concealment. This suggests that nest concealment is the most important variable influencing nesting success at this site, which has a preponderance of visually-oriented predators.     

THE BIRDS OF LANGEBAAN LAGOON

Data are presented on breeding success of Red Bishops (Euplectes orix) collected over four breeding seasons at a colony in the Addo Elephant National Park, Eastern Cape, South Africa. Overall hatching and fledging success were 53.8% and 26.0% of all eggs laid, respectively, and the overall mean number of fledglings per breeding attempt was 0.77. Hatching and fledging success varied significantly among seasons, with both clutch and brood losses due to predation being the main reason for the observed differences. Hatching success also differed significantly among clutch sizes, being highest for four-egg clutches (63.2%), intermediate for three-egg clutches (55.5%) and lowest for two-egg clutches and five-egg clutches (33.2% and 34.3%, respectively). However, fledging success was not significantly different among clutch sizes. The mean number of fledglings per breeding attempt was 0.44 for two-egg clutches, 0.80 for three-egg clutches, 1.10 for four-egg clutches, and 0.57 for five-egg clutches. The height of accepted nests (i.e.nests in which at least one egg was laid) was significantly lower than the height of nests not accepted. In addition, accepted nests in which eggs hatched and young fledged were significantly lower than accepted nests in which no eggs hatched and no young fledged. These overall effects of nest height on nest acceptance and hatching and fledging success were, however, due only to nests built above water, since no such effects were found when nests built above ground (i.e.on dry land) were analysed separately. I detected no effect of nest coverage on the probability of a nest being accepted, nor was there any effect of nest coverage on hatching or fledging success. Nests above water were significantly more likely to be accepted than nests above ground; however, hatching and fledging success of nests that were accepted did not differ significantly between nests built above water and those built above ground.     

Reproductive tactics under severe egg predation: an eider’s dilemma

Parental defence against predators may increase offspring survival but entail other costs. Egg predation is frequent early in the laying sequence of the common eider, which differs in this and in several other ways from most other waterfowl. We test the hypothesis that permanent presence at the nest from the second or third egg is an adaptation for reducing egg predation in eiders. Two other alternative hypotheses for lower predation at later nest stages are early predation loss of the most vulnerable nests and seasonal decrease in predation risk. Analyses of predation rates at the one-egg and later stages refute these two alternatives. Early nest attendance by eider females is estimated to increase clutch survival by about 20% in four-egg and 35% in five-egg clutches, albeit probably at a cost of smaller clutch size.     

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.     

Factors affecting the responses of female Canada Geese to disturbance during incubation

During incubation, Canada Geese (Branta canadensis) and other waterfowl flush from their nests in response to the approach of potential predators and subsequently return to nests after the threat of predation has abated. Differences among individuals in their responses to such disturbance (e.g., how close a potential predator approaches before flushing) are thought to reflect variation in female age, the reproductive value of clutches, and nest site characteristics. From 26 April to 26 May 2010, we examined the possible effects of these factors on the behavior of female Canada Geese (B. c. interior) on Akimiski Island, Nunavut. We used humans as surrogate predators and flushing distance and return time after disturbance as response variables. The distance at which females flushed in response to approaching humans was best explained by the density of vegetation around nests, with females on better concealed nests flushing at closer distances. We also found a weak relationship between return time and clutch size, with females with larger clutches returning to nests sooner. The frequency of human visits did not affect either female flushing distance or return time. Female Canada Geese in our study appeared to minimize risk of their own injury or death (future reproductive potential) in escape decisions, whereas return times appeared to minimize the risk of nest predation (current reproductive investment).     

Vegetation structure influences predation rates of early nests in subarctic breeding waders

Ground-nesting species are vulnerable to a wide range of predators and often experience very high levels of nest predation. Strategies to reduce nest vulnerability can include concealing nests in vegetation and/or nesting in locations in which nests and eggs are camouflaged and less easy for predators to locate. These strategies could have important implications for the distribution of ground-nesting species and the success rates of nests in areas with differing vegetation structure. However, the factors influencing the success of nest concealment and camouflage strategies in ground-nesting species are complex. Here we explore the effects of local vegetation structure and extent of nest concealment on nest predation rates in a range of ground-nesting, sympatric wader species with differing nest concealment strategies (open-nest species: Oystercatcher Haematopus ostralegus, Golden Plover Pluvialis apricaria and Whimbrel Numenius phaeopus; concealed-nest species: Black-tailed Godwit Limosa limosa, Redshank Tringa totanus and Snipe Gallinago gallinago) in south Iceland, in landscapes that comprise substantial variability in vegetation structure at a range of scales. We monitored 469 nests of these six wader species in 2015 and 2016 and ~40% of these nests were predated. Nest predation rates were similar for open-nest and concealed-nest species and did not vary with vegetation structure in the surrounding landscape, but nest-concealing species were ~10% more likely to have nests predated when they were poorly concealed, and the frequency of poorly concealed nests was higher in colder conditions at the start of the breeding season. For concealed-nest species, the reduced capacity to hide nests in colder conditions is likely to reflect low rates of vegetation growth in such conditions. The ongoing trend for warmer springs at subarctic latitudes could result in more rapid vegetation growth, with consequent increases in the success rates of early nests of concealed-nest species. Temperature-related effects on nest concealment from predators could thus be an important mechanism through which climate change affecting vegetation could have population-level impacts on breeding birds at higher latitudes.     

Appearance and vulnerability of artificial duck nests to avian predators

Use of artificial nests in studies of nest success in birds has become increasingly popular, but this practice has been criticised because the appearance and success of artificial nests may differ from natural nests. Typically, artificial nests are presented with few visible eggs throughout the entire exposure period while natural nests during their life have different appearances, possibly producing stage-dependent predation rates. In ducks, nests may appear with openly visible eggs, eggs covered with nest material and covered by an incubating female. To test how nest appearance may affect nest survival, I simulated such duck nest appearances, and used direct observations to record responses of marsh harriers Circus aeruginosus , the dominant duck nest predator at the Lake Engure, Latvia, during the breeding seasons 2000–2002. I recorded 274 harrier flights over all types of artificial nests, 74 nest discoveries and 54 predation events. Logistic regression analyses showed that nest appearance was a significant predictor of the fate of the nest: nests with openly visible eggs were discovered more often than nests covered with nest material. Nests with dummy females had discovery rates similar to the average of all artificial nest types suggesting that they best reflect the predation risk of artificial nests and could be used in future studies. After discovering nests covered with dummy females, harriers never attacked but tried to scare them off to get access to the eggs. In 52% of cases of nest discovery, harriers gave up before touching the dummy. This shows that duck passive nest defence may prevent clutch predation.     

Nest concealment is associated with reproductive traits across sympatric bird species

Nest‐site characteristics are thought to play an important role in reproductive performance in birds (e.g., influencing reproductive success and predation risk). Nest‐site characteristics such as concealment may be particularly critical at high elevation where nests are exposed to challenging environmental conditions. In this study, we conducted both conventional and phylogenetically controlled analyses to investigate whether nest concealment affected several reproductive traits across 21 sympatric bird species living on Tibet Plateau (3,400 m altitude). Qualitatively equivalent results were reached in analyses, regardless of phylogenetic controls. We found that clutch size, incubation period, nestling period, and nest success were strongly and positively associated with nest concealment across species. Our study addressed such a high‐elevation bird community that is lacking in the previous studies. This study adds to theory that while there are a few exceptions, overall evidence supports a positive effect of nest concealment on reproductive performance across coexisting alpine species.