Birds often face various stressors during feather renewing, for example, enduring infection with blood parasites. Because nutritional resources are typically limited, especially for wild animals, when an individual allocates energy to one physiological system, there is subsequently less for other processes, thereby requiring a trade‐off. Surprisingly, potential trade‐offs between malaria infection and feather growth rate have not been experimentally considered yet. Here, we conducted three studies to investigate whether a trade‐off occurs among feather growth rate, malaria infection and host health conditions. First, we explored whether naturally infected and uninfected house sparrows differed in feather growth rate in the wild. Second, we asked whether experimental inoculation of malaria parasites and/or forcing the renewal of a tail feather. Lastly, we evaluated whether individual condition was affected by experimentally‐induced feather regrowth and/or malaria experimental infection. Our findings showed that feather growth rate was negatively affected by natural malaria infection status in free‐living birds and by experimental infection in captive birds. Furthermore, birds that did not increase body mass or hematocrit during the experimental study had slower feather growth. Together our results suggest that infection with blood parasites has more negative health effects than the growth of tail feathers and that these two processes (response to blood parasite infection and renewal of feathers) are traded‐off against each other. As such, our results highlight the role of malaria parasites as a potential mechanism driving other trade‐offs in wild passerines.
Many organisms engage in metabolic tradeoffs to manage costs associated with reproductive output which often leads to these costs carrying over into the future. Compensatory mechanisms vary across life history strategies and are expected to result in near-optimal fitness gains for the investor. Here we investigated whether environmental differences associated with increasing montane elevation and variation in reproductive output of a resident passerine songbird, the Mountain Chickadee (Poecile gambeli), were related to physiological conditions during annual molt. Higher elevations are associated with harsher environmental conditions during the winter, which results in later and shorter breeding seasons than at lower elevations. We sampled the outermost tail feathers from adult birds in the fall after their prebasic molt, which initiates closely after reproduction (e.g., after parental care has ceased, ~1–3 weeks). We measured the hormone corticosterone deposited in feathers (fCORT) and feather growth rates for evidence of physiological effort predicted to be driven by several units of reproductive output (e.g., breeding timing, clutch and brood size, and offspring mass). There were no relationships between any measure of reproductive output and feather characteristics between elevations or across years, despite substantial variation in reproductive output in the wider population across this same time. However, birds at the high-elevation site grew their tail feathers significantly faster and had higher fCORT deposition compared to low-elevation birds. These results suggest that although differences in reproductive output and any related signals of associated physiological effort (e.g., fCORT and feather growth rate) may not extend into individual conditions during annual molt, shorter breeding seasons associated with harsher environmental conditions may favor faster feather growth as required by earlier onset of winter.
more » « less- NSF-PAR ID:
- 10508335
- Publisher / Repository:
- Oxford University Press
- Date Published:
- Journal Name:
- Ornithology
- ISSN:
- 0004-8038
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Laboratory studies show that increased physiological burden during development results in cognitive impairment. In the wild, animals experience a wide range of developmental conditions, and it is critical to understand how variation in such conditions affects cognitive abilities later in life, especially in species that strongly depend on such abilities for survival. We tested whether variation in developmental condition is associated with differences in spatial cognitive abilities in wild food-caching mountain chickadees. Using tail feathers grown during development in juvenile birds, we measured feather corticosterone (Cort f ) levels and growth rates and tested these birds during their first winter on two spatial learning tasks. In only 1 of the 3 years, higher feather Cort f was negatively associated with memory acquisition. No significant associations between feather Cort f and any other measurement of spatial cognition were detected in the other 2 years of the study or between feather growth rate and any measurement of cognition during the entire study. Our results suggest that in the wild, naturally existing variation in developmental condition has only a limited effect on spatial cognitive abilities, at least in a food-caching species. This suggests that there may be compensatory mechanisms to buffer specialized cognitive abilities against developmental perturbations.more » « less
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Abstract The ability of animals to sync the timing and location of molting (the replacement of hair, skin, exoskeletons or feathers) with peaks in resource availability has important implications for their ecology and evolution. In migratory birds, the timing and location of pre-migratory feather molting, a period when feathers are shed and replaced with newer, more aerodynamic feathers, can vary within and between species. While hypotheses to explain the evolution of intraspecific variation in the timing and location of molt have been proposed, little is known about the genetic basis of this trait or the specific environmental drivers that may result in natural selection for distinct molting phenotypes. Here we take advantage of intraspecific variation in the timing and location of molt in the iconic songbird, the Painted Bunting (
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ABSTRACT Populations of Vaux’s Swift (Chaetura vauxi), like those of many aerial insectivores, are rapidly declining. Determining when and where populations are limited across the annual cycle is important for their conservation. Establishing the linkages between wintering and breeding sites and the strength of the connections between them is a necessary first step. In this study, we analyzed 3 stable isotopes (δ13C, δ15N, δ2H) from feathers collected during spring migration from Vaux’s Swifts that perished during a stopover on Vancouver Island, British Columbia, Canada. We previously analyzed claw tissue (grown during winter) from the same individuals, revealing that the swifts likely wintered in 2 or 3 locations/habitats. Here, we used stable isotope analysis of flight feathers presumed to have been grown on, or near, the breeding grounds to determine the likely previous breeding locations and presumed destinations for the swifts. Stable isotope values (δ13C, δ15N, δ2H) showed no meaningful variation between age classes, sexes, or with body size. Surprisingly, ~26% of the birds sampled had feather isotope values that were not consistent with growth on their breeding grounds. For the remaining birds, assigned breeding origins appeared most consistent with molt origins on Vancouver Island. Overall, migratory connectivity of this population was relatively weak (rM = 0.07). However, the degree of connectivity depended on how many winter clusters were analyzed; the 2-cluster solution suggested no significant connectivity, but the 3-cluster solution suggested weak connectivity. It is still unclear whether low migratory connectivity observed for Vaux’s Swift and other aerial insectivores may make their populations more or less vulnerable to habitat loss; therefore, further efforts should be directed to assessing whether aerial insectivores may be habitat limited throughout the annual cycle.
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