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1.
J Evol Biol ; 18(2): 481-95, 2005 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15715854

RESUMO

The ability of organisms to respond evolutionarily to rapid climatic change is poorly known. Secondary sexual characters show the potential for rapid evolutionary change, as evidenced by strong divergence among species and high evolvability. Here we show that the length of the outermost tail feathers of males of the socially monogamous barn swallow Hirundo rustica, feathers that provide a mating advantage to males, has increased by more than 1 standard deviation during the period from 1984 to 2003. Barn swallows from the Danish population studied here migrate through the Iberian Peninsula to South Africa in fall, and return along the same route in spring. Environmental conditions on the spring staging grounds in Algeria, as indexed by the Normalized Difference Vegetation Index, predicted tail length and change in tail length across generations. However, conditions in the winter quarters and at the breeding grounds did not predict change in tail length. Environmental conditions in Algeria in spring showed a temporal deterioration during the study period, associated with a reduction in annual survival rate of male barn swallows. Phenotypic plasticity in tail length of males, estimated as the increase in tail length from the age of 1 to 2 years, decreased during the course of the study. Estimates of directional selection differentials for male tail length with respect to mating success, breeding date, fecundity, survival and total selection showed temporal variation, with the intensity of breeding date selection, survival selection and total selection declining during the study. Response to selection as estimated from the product of heritability and total selection was very similar to the observed temporal change in tail length. These findings provide evidence of rapid micro-evolutionary change in a secondary sexual character during a very short time period, which is associated with a rapid change in environmental conditions.


Assuntos
Evolução Biológica , Clima , Seleção Genética , Caracteres Sexuais , Andorinhas/anatomia & histologia , Argélia , Análise de Variância , Animais , Pesos e Medidas Corporais , Dinamarca , Plumas/anatomia & histologia , Análise de Sobrevida , Cauda/anatomia & histologia , Fatores de Tempo
4.
Oecologia ; 125(2): 201-207, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24595831

RESUMO

Parasites often have detrimental effects on their hosts, and only host individuals able to cope with parasitism are likely to display induced or genetic resistance. Hosts may respond to parasitism by differential investment in offspring depending on their ability to cope with parasitism, because offspring that perform better than their siblings are themselves likely to have superior induced or genetic resistance. We tested whether nestlings of the highly colonial sand martin Riparia riparia were affected by the haematophagous tick Ixodes lividus by experimentally manipulating parasite loads of nests [nests sprayed with pyrethrum to remove parasites (sprayed), or nests sprayed with water (control)] at three stages of the breeding season. Prevalence and intensity of ticks were significantly affected by treatments. Breeding success was not significantly affected by treatment, although post-fledging survival was twice as high among nestlings from sprayed nests than from controls. Mean phenotypic traits of nestlings generally did not differ significantly among treatments, while within-brood variance in keel length (a skeletal character) and body mass were higher in control treatment broods than sprayed ones. Sedimentation rate, which reflects blood protein and immunoglobulin content, was significantly higher and less variable in sprayed than control broods. These findings are consistent with the suggestion that parasitism effects on host reproductive success act through an increase in the variance of offspring quality.

5.
Oecologia ; 119(1): 9-15, 1999 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28308163

RESUMO

Parent-offspring conflict may arise because the lifetime reproductive success of the parent is more influenced by its life span than by reproductive success during a particular reproductive event, while the fitness of an offspring depends firstly on its own survival as a juvenile and only subsequently on its own reproductive success. The naive immune system of young animals may allow offspring to be much more affected by parasites than their parents, and thus cause an initial asymmetry in a potential parent-offspring conflict. We investigated this type of conflict by assessing the health status and the immune response of parent and offspring sand martins Riparia riparia infested with manipulated loads of ticks Ixodes lividus (nests either treated with pyrethrin, water, or just visited). The prevalence and the intensity of tick infestations differed among treatments, with low tick loads in nests with the pyrethrin treatment. Ticks reduced the reproductive success of the host and increased offspring wing length. Broods with ticks had higher leukocyte concentrations and concentrations of immunoglobulins. The concentration of immunoglobulins in nestlings was negatively related to brood size and nestling tarsus length. Nestlings receiving the control treatments had a positive association between wing length and the concentration of immunoglobulins and a negative association between tarsus length and immunoglobulins. In contrast, adult sand martins did not respond to the parasite treatment in terms of immune response. Hence, the naive immune system of nestlings may be the crucial factor causing the parent-offspring conflict over costs of parasitism to be resolved to the advantage of parents that may sacrifice nestlings in heavily parasitized nests.

6.
Oecologia ; 78(4): 490-495, 1989 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28312178

RESUMO

We tested two general models of flocking behaviour, namely the antipredation model and foraging efficiency model on mixed-species tit flocks (Parus spp.). After food addition the size of mixed-species flocks was significantly less than in the control samples. In the presence of extra food significantly more birds were observed either in monospecific flocks or solitary, than during the control observations. In the presence of a living predator the birds foraged in larger mixed-specifies flocks than during the control observations. In addition, the social behaviour of Great Spotted Woodpecker, Middle Spotted Woodpecker and Nuthatch shifted to mixed-specific flocking. The size of monospecific flocks was independent of both treatments. The density of birds increased significantly after food addition, while in the predator presence the birds tended to leave the forest. These results support the view that both the antipredation model and foraging efficiency model seem to be valid for mixed-species flocking. However, in the case of monospecific flocks, the territory maintenance could be the most important factor.

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