Social stimulation,nuptial colouration,androgens and immunocompetence in a sexual dimorphic cichlid fish

The nature of the costs maintaining honesty of sexual signalling in inter- and intrasexual interactions remains a contentious issue. For carotenoid-based colour ornaments, it has been hypothesized that the honesty of the signal is enforced when carotenoid allocation to colour expression is traded off against carotenoid availability for immunocompetence. In addition, honesty is enforced if androgens required for colour expression are immunosuppressive. We tested whether there is a trade-off between colour expression and immunocompetence in a lek-breeding haplochromine cichlid fish, Pundamilia nyererei, from Lake Victoria with a carotenoid-based nuptial dress. First, we showed that expression of red nuptial colouration and social rank in a group were positively correlated. We then successfully manipulated the level of colour advertisement by socially stimulating individually housed males with a rival male: Stimulated males developed larger areas of red nuptial colouration and had higher levels of circulating 11-ketotestosterone (11-KT) than non-stimulated males. We subsequently tested the humoral immune response to a novel antigen (sheep red blood cells). There was no overall significant effect of social stimulation on antibody production, but in the stimulated males, the degree of red colouration and the antibody response were negatively correlated. This significant interaction between colour and treatment thus shows that the negative correlation between colouration and antibody production is dependent on the (manipulated) social environment. This study provides correlational and experimental evidence for a trade-off between expression of a sexual trait and one component of immune function in fish. We found no evidence for a direct effect of 11-KT on antibody production, and we discuss alternative mechanisms that could mediate the trade-off.     

The relative role of age and experience in determining variation in body mass during the early breeding career of the Common Tern (<Emphasis Type="Italic">Sterna hirundo</Emphasis>)

Body mass is a consistent individual trait that characterises the state of adult birds and mammals and is positively related with long-term reproductive success. However, whether and to what extent body mass changes over lifetime in long-lived birds is poorly studied. In this paper, we investigate how individual body mass varies with age. Furthermore, we try to separate possible effects of age and experience on body mass. This study was conducted in a Common Tern colony on the German Wadden Sea coast. Transponders allowed registration of individuals throughout the breeding season and consecutive years with an antenna system combined with electronic balances for recording individual body-mass changes within and between years. Individual body masses of males and females were measured during three stages of the breeding season: at arrival, during incubation and chick rearing when mass was lowest in both sexes. Individual-based longitudinal analyses clearly showed that body mass during arrival, incubation and chick rearing increased up to an age of 5 or 6 years. First-time breeders had lower body mass than experienced breeders. Experience had stronger effects on incubation mass than age. Recruiting age also affected body-mass development of breeders: Three-year-old recruits showed a stronger increase in mass with experience than 4-year-old recruits. We assume that increasing experience enables birds to cope better with the physiological challenge of reproduction. To explain the general phenomenon of higher body mass in older birds, our results support the constraint hypothesis rather than either the selection or restraint hypothesis.     

Shared paternity in the acorn woodpecker (Melanerpes formicivorus)

Summary We investigated multiple paternity in acorn woodpeckers (Melanerpes formicivorus) from central New Mexico by starch-gel electrophoresis. Seven of thirty-one presumptive genetic loci were polymorphic. Multiple paternity was revealed in one of three multi-male groups sampled on the basis of offspring and adult electrophoretic phendtypes, and was suggested in the two other groups. This study provides the first documentation of multiple paternity for any avian cooperative breeder.     

Effects of predation risk and hunger on the behaviour of two species of tadpoles

Predation and hunger are threats for most organisms, and appropriate behavioural responses to both factors should be shaped by natural selection. In combination, however, the behavioural demands of predation avoidance and effective foraging often cannot be satisfied at the same time and lead to a conflict within organisms. We examined the behavioural responses of two closely-related species of tadpoles, Rana lessonae and R. esculenta, to simulated predation by fish and hunger. Tadpoles, hatched and reared in the laboratory, were tested in a three-way factorial (predation risk × hunger × species) experiment with four predation levels and four hunger levels. Both species decreased their swimming activity with increasing predation risk. Predation risk did not influence the amount of activity time invested in feeding but caused the tadpoles to spend less time in patches with food. Refuges were not used to avoid predation. R. esculenta was more sensitive to predation risk than R. lessonae. Hunger increased both the activity of tadpoles and the amount of activity time invested in feeding, thus indicating an increased energy intake. No interactions were observed between predation risk and hunger. These results show that tadpoles possess genetically-based behavioural mechanisms that allow them to respond in a graded manner to predation and hunger. However, they did not balance the two conflicting demands of predation avoidance and effective foraging; the two mechanisms appeared to act independently. Correspondence to: R.D. Semlitsch     

Sexual selection and cuckoldry in a monogamous songbird: implications for sexual selection theory

Sexual selection is generally assumed to be weaker in monogamous than in polygynous animals. Recently, though, extra-pair fertilizations have been hailed as an important force in generating variance in reproductive success among males in socially monogamous species, thereby increasing the intensity of sexual selection. To see if extra-pair copulations contribute to variance in male reproductive success in the house finch (Carpodacus mexicanus), we used DNA fingerprinting to determine the paternity of chicks from 35 nests. This species is a socially monogamous passerine in which plumage brightness serves as a sexually selected indicator of male quality. Out of 119, nestlings 10 (8.3%) were fathered by a male other than the attending male, but cuckoldry occurred randomly with respect to the plumage colouration, size, or age of the attending male. Thus extra-pair fertilizations do not generate variance in male reproductive success with respect to plumage colour. On the other hand, a strongly male-biased sex ratio and asynchronous breeding by females may generate substantial variance in male reproductive success and could explain the evolution of ornamental colouration.     

“Chance” and mixed-species associations

Summary Spatial associations between members of different animal species may arise through mutual behavioral attraction, through attraction to common resources or locations, or by chance. I outline a means of calculating the expected duration of associations based on the null hypothesis that members of different species move independently and randomly. Observed association durations can be compared to these expectations to identify those cases of association (or avoidance) that have biologically interesting causes. The method is applicable to any species in which the presence of a second species can be recorded during focal samples of an individual or a cohesive social group. The data required are readily collected in the field; I illustrate the use of the technique with data from several East African forest primates.     

Complex brood care and reproductive behaviour in captive poison-arrow frogs,Dendrobates pumilio O. Schmidt

Summary Brood care in Dendrobates pumilio not only involves egg attendance and tadpole transport, but also tadpole attendance and feeding. Each tadpole is carried by the attending female to a water-filled bromelial leaf axil and regularly fed on unfertilized eggs. The tadpole responds to an approaching adult with a specialized, conspicuous behavior signalling its presence. Male-male competition includes fighting, egg eating, and male tadpole transport. D. pumilio is the first frog known to feed its free-living larvae.     

The use of the tergal gland defensive secretion in male intrasexual aggression of the rove beetle,Aleochara curtula (Coleoptera: Staphylinidae), measured by closed-loop-stripping-analyses and tandem bioassay — mass fragmentography

Summary 2-methyl-1,4-benzoquinone as a target compound of the tergal gland secretion of the rove beetle,Aleochara curtula, was quantified from the reservoirs of individual beetles. Males store less secretion than females, and they evaporate more of the secretion as measured by adsorption from the air (closed-loop-stripping-analysis). The amount of emitted quinone is increased during aggressive interactions of rival males. The pulsed emission of the secretion during aggression is demonstrated by a novel technique combining observation of behavior with the on-line measurement of target fragment ions by mass-spectrometry (tandem bioassay — mass fragmentography). The emission of the secretion is used as a weapon in combats between males and may result in the repulsion of subordinate males from the mating site, but may also serve to mimic females chemically in order to avoid aggressive encounters.     

Biological markets: supply and demand determine the effect of partner choice in cooperation,mutualism and mating

The formation of collaborating pairs by individuals belonging to two different classes occurs in the contexts of reproduction and intea-specific cooperation as well as of inter-specific mutualism. There is potential for partner choice and for competition for access to preferred partners in all three contexts. These selective forces have long been recognised as important in sexual selection, but their impact is not yet appreciated in cooperative and mutualistic systems. The formation of partnerships between members of different classes has much in common with the conclusion of trade agreements in human markets with two classes of traders, like producers and consumers, or employers and employees. Similar game-theoretical models can be used to predict the behaviour of rational traders in human markets and the evolutionarily stable strategies used in biological markets. We present a formal model in which the influence of the market mechanism on selection is made explicit. We restrict ourselves to biological markets in which: (1) Individuals do not compete over access to partners in an agonistic manner, but rather by outcompeting each other in those aspects that are preferred by the choosing party. (2) The commodity the partner has to offer cannot be obtained by the use of force, but requires the consent of the partner. These two restrictions ensure a dominant role for partner choice in the formation of partnerships. In a biological market model the decision to cooperate is based on the comparison between the offers of several potential partners, rather than on the behaviour of a single potential partner, as is implicitly assumed in currently accepted models of cooperation. In our example the members of one class A offer a commodity of fixed value in exchange for a commodity of variable value supplied by the other class, B. We show that when the B-class outnumbers the A-class sufficiently and the cost for the A-class to sample the offers of the B-class are low, the choosiness of the A-class will lead to selection for the supply of high value commodities by the B-class (Fig. 3a). Under the same market conditions, but with a high sampling cost this may still be the evolutionariy stable outcome, but another pair of strategies proves to be stable too: relaxed choosiness of class A coupled with low value commodities supplied by class B (Fig. 3b). We give a number of examples of mating, cooperative and mutualistic markets that resemble the low sampling cost situation depicted in Fig. 3a.