期刊
MOLECULAR ECOLOGY
卷 28, 期 15, 页码 3464-3481出版社
WILEY
DOI: 10.1111/mec.14999
关键词
alternative reproductive tactics; androgens; neuroendocrine; sexual selection; social behaviour; teleosts
While extensive research has focused on how social interactions evolve, the fitness consequences of the neuroendocrine mechanisms underlying these interactions have rarely been documented, especially in the wild. Here, we measure how the neuroendocrine mechanisms underlying male behaviour affect mating success and sperm competition in the ocellated wrasse (Symphodus ocellatus). In this species, males exhibit three alternative reproductive types. Nesting males provide parental care, defend territories and form cooperative associations with unrelated satellites, who cheat by sneaking fertilizations but help by reducing sperm competition from sneakers who do not cooperate or provide care. To measure the fitness consequences of the mechanisms underlying these social interactions, we used phenotypic engineering that involved administering an androgen receptor antagonist (flutamide) to wild, free-living fish. Nesting males treated with flutamide shifted their aggression from sneakers to satellite males and experienced decreased submissiveness by sneaker males (which correlated with decreased nesting male mating success). The preoptic area (POA), a region controlling male reproductive behaviours, exhibited dramatic down-regulation of androgen receptor (AR) and vasotocin 1a receptor (V1aR) mRNA following experimental manipulation of androgen signalling. We did not find a direct effect of the manipulation on male mating success, paternity or larval production. However, variation in neuroendocrine mechanisms generated by the experimental manipulation was significantly correlated with changes in behaviour and mating success: V1aR expression was negatively correlated with satellite-directed aggression, and expression of its ligand arginine vasotocin (AVT) was positively correlated with courtship and mating success, thus revealing the potential for sexual selection on these mechanisms.
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