Feathers in the spotless starling nests: a sexually selected trait?

Behaviour ◽  
2011 ◽  
Vol 148 (11-13) ◽  
pp. 1355-1371 ◽  
Author(s):  
José P. Veiga ◽  
Vicente Polo

AbstractThe carrying of feathers to adorn the nest has been recently described as a female behaviour that indicates quality in a passerine bird — the spotless starling (Sturnus unicolor) —, but the consequences that the variability of this trait may have on breeding success are still unknown. The feather-carrying behaviour is a sexual behaviour that is performed in response to a male display: the carrying of green plants. In this paper we explore whether foreign feathers affect male investment on chick rearing or reinforce the pair mating bonds. The experimental addition of feathers to nests caused an increase in clutch size and a reduction of nestling mortality, although it did not affect feeding rates or the removal of faecal sacs by males or females. Nest feathers did not increase the frequency with which females laid a second clutch in the same nest and with the same male. Thus, our results do not support the sexual selection hypothesis for the evolution of the carrying feathers behaviour. An alternative hypothesis that deserves to be addressed in specifically designed studies is that foreign feathers may be taken to nests as a sort of chemical warfare against nest parasites. The sexual selection and the chemical defence hypotheses are, however, not mutually exclusive and future research should evaluate whether the pre-existence of a behavioural trait arising by natural selection may drive the evolution of a signalling trait.

2013 ◽  
Vol 16 (2) ◽  
pp. 160-174 ◽  
Author(s):  
Debra Lyon ◽  
Lynne Elmore ◽  
Noran Aboalela ◽  
Jacqueline Merrill-Schools ◽  
Nancy McCain ◽  
...  

Due to recent treatment advances, there have been improvements in the proportion of women surviving a diagnosis of breast cancer (BC). However, many of these survivors report persistent adverse side effects following treatment, such as cognitive dysfunction, depressive symptoms, anxiety, fatigue, sleep disturbances, and pain. Investigators have examined circulating levels of inflammatory markers, particularly serum cytokines, for a potential causal relationship to the development/persistence of these psychoneurological symptoms (PNS). While inflammatory activation, resulting from perceived stress or other factors, may directly contribute to the development of PNS, we offer an alternative hypothesis, suggesting that these symptoms are an early step in a cascade of biological changes leading to epigenetic alterations at the level of deoxyribonucleic acid (DNA) methylation, histone modifications, and/or chromatin structure/chromosomal instability. Given that epigenetic patterns have plasticity, if this conjectured relationship between epigenomic/acquired genomic alterations and the development/persistence of PNS is confirmed, it could provide foundational knowledge for future research leading to the recognition of predictive markers and/or treatments to alleviate PNS in women with BC. In this article, we discuss an evolving theory of the biological basis of PNS, integrating knowledge related to inflammation and DNA repair in the context of genetic and epigenetic science to expand the paradigm for understanding symptom acquisition/persistence following chemotherapy.


The Auk ◽  
1984 ◽  
Vol 101 (2) ◽  
pp. 274-280 ◽  
Author(s):  
Helen Hays

Abstract In this paper I report the first instance of a pair of Common Terns (Sterna hirundo) raising young in successive clutches during one breeding season and discuss this phenomenon in relation to male and female incubation and feeding rates and to predation. Five other pairs are noted in which the female and sometimes the male incubated a second clutch while still feeding one young from their first nest.


Author(s):  
Yael Sela ◽  
Nicole Barbaro

Religion motivates, exacerbates, and even justifies violence. This chapter argues that religious beliefs regarding violence—particularly those of monotheistic, Abrahamic faiths—are shaped by evolved psychological mechanisms. Further, it argues that religiously motivated violence is most likely to occur in evolutionarily relevant contexts. Guided by sexual selection theory and parental-investment theory, it first provides an overview of human sexual selection from an evolutionary perspective. It discusses how and why an evolutionary perspective—and principles of sexual selection and parental investment in particular—may provide a richer understanding of religiously motivated violence. Next follows an overview of research addressing several types of religiously motivated violence such as mate guarding and controlling behaviors, wife beating and uxoricide, honor killing, child abuse and filicide, male and female genital mutilation, war, and terrorism. Finally, it highlights the parallels between religiously motivated violence and evolved psychological mechanisms for violence, concluding with suggestions for future research.


Nature ◽  
2000 ◽  
Vol 407 (6807) ◽  
pp. 1000-1003 ◽  
Author(s):  
Erick Greene ◽  
Bruce E. Lyon ◽  
Vincent R. Muehter ◽  
Laurene Ratcliffe ◽  
Steven J. Oliver ◽  
...  

2013 ◽  
Vol 280 (1771) ◽  
pp. 20132175 ◽  
Author(s):  
Daniel T. Baldassarre ◽  
Michael S. Webster

Theory suggests that traits under positive selection may introgress asymmetrically across a hybrid zone, potentially driven by sexual selection. Two subspecies of the red-backed fairy-wren ( Malurus melanocephalus ) differ primarily in a sexual signal used in mate choice—red versus orange male back plumage colour—but phylogeographic analyses suggest asymmetrical introgression of red plumage into the genetic background of the orange subspecies. We hypothesized that this asymmetrical introgression may be facilitated by sexual selection if red males have a mating advantage over orange males. We tested this hypothesis with correlational data and a plumage manipulation experiment where we reddened the back plumage of a subset of orange males to mimic males of the red subspecies. There was no correlational evidence of a mating advantage to naturally redder males in this population. Experimentally reddened males sired a similar amount of within-pair young and lost paternity at the same rate as orange males, but they sired significantly more extra-pair young, leading to substantially higher total reproductive success. Thus, we conclude that sexual selection via extra-pair mating is a likely mechanism responsible for the asymmetrical introgression of plumage colour in this system, and is potentially driven by a sensory bias for the red plumage signal.


2014 ◽  
Vol 126 (1) ◽  
pp. 9-18 ◽  
Author(s):  
Linda A. Whittingham ◽  
Peter O. Dunn

Population genetic models have shown that female choice is a potential cause of the evolution of male display. In these models the display is assumed to be the immediate object of female choice. Here I present an explicit genetic model that shows that male display can evolve as a consequence of female choice even when the display is not the immediate object of choice. When females initially base their preferences on the existence of variance in a cue that is correlated with male viability, a rare display can evolve to fixation if it amplifies the previously recognized differences in males, (i. e. if it increases the resolution power of females with respect to the original cue). By definition, amplifying displays (or amplifiers) increase mating success of the more viable males and decrease mating success of the less viable males. Therefore, the higher the frequency of the preferred, more viable males, the more likely it is that amplifiers will evolve to fixation. The evolution of an amplifier is further facilitated by a genetic association that is built up between the amplifier allele and the more viable allele. If the expression of the amplifier is limited to the more viable males, the amplifier will evolve to fixation provided only that the change in total fitness to the more viable males (higher mating success, lower viability), is positive.


Evolution ◽  
2006 ◽  
Vol 60 (4) ◽  
pp. 856-868 ◽  
Author(s):  
A. P. Møller ◽  
Y. Chabi ◽  
J. J. Cuervo ◽  
F. Lope ◽  
J. Kilpimaa ◽  
...  

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