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  1. Abstract Aim

    Physiological tolerances and biotic interactions along habitat gradients are thought to influence species occurrence. Distributional differences caused by such forces are particularly noticeable on tropical mountains, where high species turnover along elevational gradients occurs over relatively short distances and elevational distributions of particular species can shift among mountains. Such shifts are interpreted as evidence of the importance of spatial variation in interspecific competition and habitat or climatic gradients. To assess the relative importance of competition and compression of habitat and climatic zones in setting range limits, we examined differences in elevational ranges of forest bird species among four Bornean mountains with distinct features.

    Location

    Bornean mountains Kinabalu, Mulu, Pueh and Topap Oso.

    Taxon

    Rain forest bird communities along elevational gradients.

    Methods

    We surveyed the elevational ranges of rain forest birds on four mountains in Borneo to test which environmental variables—habitat zone compression or presence of likely competitors—best predicted differences in elevational ranges of species among mountains. For this purpose, we used two complementary tests: a comparison of elevational range limits between pairs of mountains, and linear mixed models with naïve occupancy as the response variable.

    Results

    We found that lowland species occur higher in elevation on two small mountains compared to Mt. Mulu. This result is inconsistent with the expectation that distributions of habitats are elevationally compressed on small mountains, but is consistent with the hypothesis that a reduction in competition (likely diffuse) on short mountains, which largely lack montane specialist species, allows lowland species to occur higher in elevation. The relative influence of competition changes with elevation, and the correlation between lower range limits of montane species and the distribution of their competitors was weaker than in lowland species.

    Main conclusions

    These findings provide support for the importance of biotic interactions in setting elevational range limits of tropical bird species, although abiotic gradients explain the majority of distribution patterns. Thus, models predicting range shifts under climate change scenarios must include not only climatic variables, as is currently most common, but also information on potentially resulting changes in species interactions, especially for lowland species.

     
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  2. Abstract

    Parents faced with a predator must choose between their own safety versus taking care of their offspring. Each choice can have fitness costs. Life‐history theory predicts that longer‐lived species should be less willing than shorter‐lived species to return to care for their offspring after a predator disturbance because they have more opportunities to reproduce in the future. We increased adult predation risk during incubation for 40 bird species in north temperate, tropical, and south temperate latitudes. We found that species with higher adult survival probabilities were more cautious, waiting longer before returning to the nest to provide care. Contrary to other studies, we also found that parents were more risk averse and waited longer to return in smaller than larger species, likely reflecting greater vulnerability of smaller species. Ultimately, the relative risk a predator poses to a species and the probability of future reproduction predict parental risk taking across the world.

     
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  3. Abstract Aim

    Adult survival is central to theories explaining latitudinal gradients in life history strategies. Life history theory predicts higher adult survival in tropical than north temperate regions given lower fecundity and parental effort. Early studies were consistent with this prediction, but standard‐effort netting studies in recent decades suggested that apparent survival rates in temperate and tropical regions strongly overlap. Such results do not fit with life history theory. Targeted marking and resighting of breeding adults yielded higher survival estimates in the tropics, but this approach is thought to overestimate survival because it does not sample social and age classes with lower survival. We compared the effect of field methods on tropical survival estimates and their relationships with life history traits.

    Location

    Sabah, Malaysian Borneo.

    Time period

    2008–2016.

    Major taxon

    Passeriformes.

    Methods

    We used standard‐effort netting and resighted individuals of all social and age classes of 18 tropical songbird species over 8 years. We compared apparent survival estimates between these two field methods with differing analytical approaches.

    Results

    Estimated detection and apparent survival probabilities from standard‐effort netting were similar to those from other tropical studies that used standard‐effort netting. Resighting data verified that a high proportion of individuals that were never recaptured in standard‐effort netting remained in the study area, and many were observed breeding. Across all analytical approaches, addition of resighting yielded substantially higher survival estimates than did standard‐effort netting alone. These apparent survival estimates were higher than for temperate zone species, consistent with latitudinal differences in life histories. Moreover, apparent survival estimates from addition of resighting, but not from standard‐effort netting alone, were correlated with parental effort as measured by egg temperature across species.

    Main conclusions

    Inclusion of resighting showed that standard‐effort netting alone can negatively bias apparent survival estimates and obscure life history relationships across latitudes and among tropical species.

     
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  4. Abstract

    Survival rates vary dramatically among species and predictably across latitudes, but causes of this variation are unclear. The rate‐of‐living hypothesis posits that physiological damage from metabolism causes species with faster metabolic rates to exhibit lower survival rates. However, whether increased survival commonly observed in tropical and south temperate latitudes is associated with slower metabolic rate remains unclear. We compared metabolic rates and annual survival rates that we measured across 46 species, and from literature data across 147 species of birds in northern, southern and tropical latitudes. High metabolic rates were associated with lower survival but survival varied substantially among latitudinal regions independent of metabolism. The inability of metabolic rate to explain latitudinal variation in survival suggests (1) species may evolve physiological mechanisms that mitigate physiological damage from cellular metabolism and (2) extrinsic rather than intrinsic sources of mortality are the primary causes of latitudinal differences in survival.

     
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  5. Abstract

    Developmental responses can help young animals reduce predation risk but can also yield costs to performance and survival in subsequent life stages with major implications for lifetime fitness. Compensatory mechanisms may evolve to offset such costs, but evidence from natural systems is largely lacking.

    In songbirds, increased nest predation risk should favour reduced provisioning, but also young that fledge (leave their nest) at an earlier age. Both responses can result in fledglings with shorter wings, reduced mobility and decreased survival. Young may compensate for shorter wings developmentally by reallocating resources towards feather development or behaviourally by adjusting flight kinematics or habitat use. However, underfed young may lack the capacity to express these phenotypes due to insufficient resources or an inability to adjust allocation of resources.

    Using predation risk experiments and 29 years of observational field data, we test whether increased nest predation risk reduces flight performance and survival during the fledgling stage and explore potential mechanisms that might underlie these effects. We show that young from high‐risk nests did not leave the nest earlier on average, but wing growth was slower likely due to observed reductions in parental feeding rates. Wings were shorter in high‐risk nests when fledglings left the nest early. Yet, fledglings from high‐risk nests showed improved flight performance for a given wing length such that flight performance at fledging did not differ between young from high‐risk and low‐risk nests. Young from high‐risk nests may have offset the costs of shorter wings on flight performance by accelerating the emergence of flight feathers from their sheaths to reduce wing porosity, though evidence for this mechanism was mixed. Fledglings from high‐risk nests also selected habitat with denser woody vegetation compared with young from low‐risk nests.

    Together, these developmental and behavioural responses seem to mitigate the expected effects of increased nest predation risk on fledgling survival. Ultimately, our results show that offspring predation risk can affect parental provisioning and offspring morphology without major implications for performance and survival in subsequent life stages.

    A freePlain Language Summarycan be found within the Supporting Information of this article.

     
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  6. Abstract

    Offspring mortality varies dramatically among species with critical demographic and evolutionary ramifications, yet the causes of this variation remain unclear. Nests are widely used for breeding across taxa and thought to influence offspring mortality risk. Traditionally, more complex, enclosed nest structures are thought to reduce offspring predation by reducing the visibility of nest contents and muffling offspring sounds compared to open nests. Direct tests of the functional bases for nest structure influence on predation risk are lacking.

    We used experiments and 10 years of observational data to examine how nest structure influences nest predation risk in a diverse community of tropical songbirds. First, we examined how nest size was related to nest structure and nest predation rates across species. Second, we assessed how nest structure influences the detectability of nestling begging calls both in field and in laboratory settings. Finally, we examined how the acoustic properties of different nest structures influence nest predation risk. Specifically, we experimentally broadcast begging calls from open and enclosed nests to determine how auditory cues and nest structure interact to affect predation on plasticine and quail eggs. We also tested whether nest structure was associated with differences in nest predation rates between the incubation (no begging cues) and nestling (begging cues) stages.

    We found that enclosed nests are larger than open nests after accounting for adult size, and larger nests had increased predation rates. Moreover, enclosed nests did not consistently alter nestling begging calls in ways that reduce the likelihood of predation compared to open nests. Indeed, begging cues increased predation rates for enclosed but not open‐cup nests in our playback experiment, and nest predation rates showed greater increases after hatching in enclosed than open‐cup nests.

    Ultimately, enclosed nests do not necessarily provide greater predation benefits than open nests in contrast to long‐standing theory.

    A freeplain language summarycan be found within the Supporting Information of this article.

     
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