Generally, paternal mouthbrooding cardinalfishes are characteristic of sex-role-reversed animals: females have a higher potential reproductive rate and are more active in mating competition than males, and the operational sex ratio (OSR) is female-biased. However, one species of cardinalfish, Apogon notatus (Houttuyn, 1782), shows unusual sex roles: females alone defend their breeding territories to form pairs, even though the OSR is male-biased. This is inconsistent with the general rule that breeding territoriality is shown by the more abundant sex. We examined the function of female breeding territory in this fish using field observations. Prior to the breeding season, large females established their territories earlier than small females. Earlier settlers occupied deeper areas with larger boulders where conspecifics were less likely to aggregate. As the level of conspecific aggregation increased, spawning females suffered from frequent intraspecific interference and subsequent egg predation, leading to increased time or energy spent on territorial defense. For the females, territories that have more boulders and fewer conspecifics might be of higher quality because such places are safe from egg predation and less costly to defend. We conclude that females defend their breeding territories to avoid predation of spawned eggs rather than to guard high-quality mates or to increase mating opportunities.
Sex-role reversal of a monogamous pipefish without higher potential reproductive rate in females