Social function of a variable lateral stripe in Xiphophorus hellerii?

In a single population of a livebearing fish, the green swordtail (Xiphophorus hellerii), a trait considered a static badge of status in males of other populations, the color of a stripe covering the lateral line, has been found to be dynamic relative to their social environment, potentially rendering this signal meaningless. Males change the color expression of their lateral stripe dynamically based on social environment. We investigated if males (n = 26) respond to visual and chemical information about other males with a color change and aggressive behavior. We found that visual information is indeed causing color change, whereas chemical information is less effective. Aggressive responses and frequency of response did not change significantly with the mode of communication. We also studied female preferences for color, but found no significant preference (n = 32). Our results lead to questions as to how interpopulation variation can affect preferences and how dynamic signaling—in this case signal transmission presumably dependent on sex and/or status—influences the behavioral interactions we might expect between X. hellerii in the field.     

Is bigger better? Male body size affects wing‐borne courtship signals and mating success in the olive fruit fly,Bactrocera oleae (Diptera: Tephritidae)

Variations in male body size are known to affect inter‐ and intrasexual selection outcomes in a wide range of animals. In mating systems involving sexual signaling before mating, body size often acts as a key factor affecting signal strength and mate choice. We evaluated the effect of male size on courtship displays and mating success of the olive fruit fly, Bactrocera oleae (Diptera: Tephritidae). Wing vibrations performed during successful and unsuccessful courtships by large and small males were recorded by high‐speed videos and analyzed through frame‐by‐frame analysis. Mating success of large and small males was investigated. The effect of male–male competition on mating success was evaluated. Male body size affected both male courtship signals and mating outcomes. Successful males showed wing‐borne signals with high frequencies and short interpulse intervals. Wing vibrations displayed by successful large males during copulation attempt had higher frequencies over smaller males and unsuccessful large males. In no‐competition conditions, large males achieved higher mating success with respect to smaller ones. Allowing large and small males to compete for a female, large males achieve more mating success over smaller ones. Mate choice by females may be based on selection of the larger males, able to produce high‐frequency wing vibrations. Such traits may be indicative of “good genes,” which under sexual selection could means good social‐interaction genes, or a good competitive manipulator of conspecifics.     

Sexual selection in mushroom-forming basidiomycetes

We expect that sexual selection may play an important role in the evolution of mushroom-forming basidiomycete fungi. Although these fungi do not have separate sexes, they do play female and male roles: the acceptance and the donation of a nucleus, respectively. The primary mycelium (monokaryon) of basidiomycete fungi, growing from a germinating sexual spore, is hermaphroditic, but it loses female function upon the acceptance of a second nucleus. The resulting dikaryon with two different nuclei in each cell retains a male potential as both nuclei can fertilize receptive mycelia. We tested the occurrence of sexual selection in the model species of mushroom-forming basidiomycetes, Schizophyllum commune, by pairing monokaryons with fully compatible dikaryons. In most pairings, we found a strong bias for one of the two nuclei although both were compatible with the monokaryon when paired alone. This shows that sexual selection can occur in mushroom-forming basidiomycetes. Since the winning nucleus of a dikaryon occasionally varied depending on the receiving monokaryon, we infer that sexual selection can operate through choosiness of the receiving individual (analogous to female choice). However, in other cases the same nucleus won, irrespective of the receiving monokaryon, suggesting that competition between the two nuclei of the donating mycelium (analogous to male–male competition) might also play a role.     

Do temperature and social environment interact to affect call rate in frogs (Crinia signifera)?

Abstract Acoustic displays are pervasive and conspicuous forms of sexual advertisement used by animals to attract mates. Evidence suggests that individuals may use environmental cues and/or the presence of other displaying animals to select the best times for display to optimize the chances of mating. Less well‐known is how the physical and social environment might interact to affect the actual content of the display itself. We examined the effects of social environment and temperature on calling rate in a frog Crinia signifera. We found that both variables interacted to affect call rate but only among continuous callers. Call rate increased with temperature in individuals calling continuously on their own but no relationship was found in frogs calling continuously in the presence of others, either in a duet or in a group calling situation. We suggest that the temperature sensitivity of calling rate in frogs could depend on the social environment of the caller. As such, we suggest caution in generalizing about the way temperature affects calling rates in frogs and encourage greater consideration of how physical and social environments might interact to influence the signal content of acoustic displays.     

Mutual ornamentation, sexual selection, and social dominance in the black swan

We investigated the adaptive significance of a sexually monomorphicornament in the black swan Cygnus atratus. Both sexes grow curledfeathers on their wings (range 7–22 curled feathers perwing), which are displayed prominently in a range of socialinteractions. The number of curled feathers increased untilthe birds reached sexual maturity (at 2 years of age) but didnot vary with age thereafter. We found evidence for both sexualand social functions of the ornament. Paired, mature individualsof both sexes had higher numbers of curled feathers than unpaired,mature birds, and individuals paired assortatively with respectto curled feather number, suggesting the feathers may be involvedin mutual sexual selection. More ornamented individuals weredominant in agonistic interactions with birds of the same sexand pairing status. Highly ornamented pairs were also more likelyto maintain extended tenancy of preferred cygnet feeding areas,which resulted in improved offspring survival. The curled feathersthus appear to function as a signal of social dominance, whichis highly correlated with reproductive success and is thereforea reliable signal of parental quality in mate choice.