Birds are known to respond to nest-dwelling parasites by altering behaviours. Some bird species, for example, bring fresh plants to the nest, which contain volatile compounds that repel parasites. There is evidence that some birds living in cities incorporate cigarette butts into their nests, but the effect (if any) of this behaviour remains unclear. Butts from smoked cigarettes retain substantial amounts of nicotine and other compounds that may also act as arthropod repellents. We provide the first evidence that smoked cigarette butts may function as a parasite repellent in urban bird nests. The amount of cellulose acetate from butts in nests of two widely distributed urban birds was negatively associated with the number of nest-dwelling parasites. Moreover, when parasites were attracted to heat traps containing smoked or non-smoked cigarette butts, fewer parasites reached the former, presumably due to the presence of nicotine. Because urbanization changes the abundance and type of resources upon which birds depend, including nesting materials and plants involved in self-medication, our results are consistent with the view that urbanization imposes new challenges on birds that are dealt with using adaptations evolved elsewhere.
Variable environments impose constraints on adaptation by modifying selection gradients unpredictably. Optimal bird development requires an adequate thermal range, outside which temperatures can alter nestling physiology, condition and survival. We studied the effect of temperature and nest heat exposure on the reproductive success of a population of double‐brooded Spotless Starlings Sturnus unicolor breeding in a nestbox colony in central Spain with a marked intra‐seasonal variation in temperature. We assessed whether the effect of temperature differed between first and second broods, thus constraining optimal nest‐site choice. Ambient temperature changed greatly during the chick‐rearing period and had a strong influence on nestling mass and all body size measures we recorded, although patterns of clutch size or nestling mortality were not influenced. This effect differed between first and second broods: nestlings were found to have longer wings and bills with increasing temperature in first broods, whereas the effect was the opposite in second broods. Ambient temperature was not related to nestling body mass or tarsus‐length in first broods, but in second broods, nestlings were lighter and had smaller tarsi with higher ambient temperatures. The exposure of nestboxes to heat influenced nestling morphology: heat exposure index was negatively related to nestling body mass and wing‐length in second broods, but not in first broods. Furthermore, there was a positive relationship between nest heat exposure and nestling dehydration. Our results suggest that optimal nest choice is constrained by varying environmental conditions in birds breeding over prolonged periods, and that there should be selection for parents to switch from sun‐exposed to sun‐protected nest‐sites as the season progresses. However, nest‐site availability and competition for sites are likely to impose constraints on this choice.
Sibling competition has been shown to affect overall growth rates in birds. However, growth consists on the coordinated development of a multitude of structures, and there is ample scope for developmental plasticity and trade-offs among these structures. We would expect that the growth of structures that are used in sibling competition, such as the gape of altricial nestlings, should be prioritized under intense competition. We conducted an experiment in the spotless starling (Sturnus unicolor), cross-fostering nestlings to nests with different levels of sibling competition. We predicted that nestlings subjected to higher levels of sibling competition should develop larger gapes than control birds. We found that, halfway through the nestling period, overall size (a composite index of mass, wing, tarsus and bill) was reduced in nests with intense sibling competition, whereas gape width remained unaffected. At the end of the nestling period, experimental nestlings had wider gapes than controls. Additionally, a correlative study showed that nestling gape width increased when feeding conditions worsened and overall size decreased. These patterns could either be due to increased growth of gape flanges or to delayed reabsorption of this structure. Our results show that birds can invest differentially in the development of organs during growth, and that the growth of organs used in sibling competition is prioritized over structural growth.
The developmental rate of cuckoo embryos and their hatching size is greater than that of host species, which may require more nutrient resources in the egg and more intensive gas exchange during development. In the present study, we compared various egg characteristics of a brood parasite, the common cuckoo Cuculus canorus, and its frequent host, the great reed warbler Acrocephalus arundinaceus. As maternally-derived testosterone is known to enhance growth rate of embryos and hatchlings, cuckoo eggs are expected to contain higher concentration of testosterone than host eggs. In addition, we expected higher concentration of antioxidants in cuckoo eggs to protect embryos from oxidative stress associated with accelerated growth. Our results showed that cuckoo eggs had thicker shells and higher pore density than great reed warbler eggs. Yolk was significantly heavier in cuckoo eggs and contained higher concentrations of carotenoids and vitamin E, however, yolk androgen and immunoglobulin concentrations were lower in cuckoo eggs as compared to great reed warbler eggs. We also examined whether eggshell colour was associated to egg quality, and detected a positive association between blue-green chroma and yolk antioxidant concentration in both species, suggesting that eggshell colour reflects the antioxidant investment of the female into the eggs. Our results suggest that cuckoo females increase the size, growth rate and competitive ability of their young by providing them with more nutrients and more dietary antioxidants for embryonic development, and not through elevated yolk testosterone or antibody levels. In addition, increased porosity of cuckoo eggshells may allow embryos to develop more rapidly because of a greater capacity of gas exchange.
There is increasing evidence that birds use chemical cues in different contexts, and this is changing the traditional view that placed birds alone as the only largely olfaction-free vertebrates. We performed a choice experiment to examine whether male house finches (C. mexicanus) exhibit any preferences for the sex of conspecifics when only their chemical cues are available. When exposed during the breeding season to the scent of a male or a female, males appeared to respond indiscriminately to both odours. However, when analysing a posteriori the choices of males in relation to their relative quality, males with worse quality than scent-donor males avoided the male-scented area, whereas males with better quality moved towards the male-scented area. Our results suggest that in the context of mate-choice/competition for mates, house finches may obtain information via olfaction to assess the quality of rival males.
The intensity of color expression in animals plays a key role in social environments as a mechanism to signal individual capacities in competitive contests. Selective pressures for resource competition differ at different stages of life and between sexes; therefore, coloration is expected to vary between juveniles and adults and between males and females. Exploring the covariance between coloration and other traits may help to understand the functional significance of color and the action of natural selection on multivariate phenotypes. Melanin-based plumage coloration was investigated in the masked booby Sula dactylatra in relation to melanin concentration, sex, hormone levels, and shy-bold behavior of chicks close to fledging. Darker brown boobies showed higher levels of both eumelanin and pheomelanin concentration and lower body mass. Males behaved bolder than females and showed on average 8% larger brown patches. Bolder females had smaller brown patches. Bolder individuals also had lower levels of circulating testosterone, but no differences in corticosterone levels were found. Stronger phenotypic integration was observed in females than males. Our study suggests that juvenile melanic coloration may reflect behavioral strategies by sex, endocrine profiles, and body mass indicating the convergence of different adaptive functions in a given phenotype, this being more evident in females. Direction of correlations differed from those predicted under the pleiotropic idea for color-related traits. These results suggest the possibility that juvenile plumage acts as a signaling system in a social context within the age class and suggest that plumage coloration may indicate different behavioral strategies.
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