Fewer than 1% of vertebrate species are hermaphroditic, and essentially all of these are fishes. Four types of hermaphroditism are known in fishes: simultaneous (or synchronous) hermaphroditism (SH), protandry (male-to-female sex change; PA), protogyny (female-to-male sex change; PG), and bidirectional sex change (BS or reversed sex change in protogynous species). Here we present an annotated list of hermaphroditic fish species from a comprehensive review and careful re-examination of all primary literature. We confirmed functional hermaphroditism in more than 450 species in 41 families of 17 teleost orders. PG is the most abundant type (305 species of 20 families), and the others are much less abundant, BS in 66 species of seven families, SH in 55 species of 13 families, and PA in 54 species of 14 families. The recently proposed phylogenetic tree indicated that SH and PA have evolved several times in not-closely related lineages of Teleostei but that PG (and BS) has evolved only in four lineages of Percomorpha. Examination of the relation between hermaphroditism type and mating system in each species mostly supported the size-advantage model that predicts the evolution of sequential hermaphroditism. Finally, intraspecific variations in sexual pattern are discussed in relation to population density, which may cause variation in mating system.
Social conditions and function of inter-group movement of females of the polygynous goby, Trimma okinawae, have been studied at Akamizu Beach, Kagoshima, Japan. Some females moved from their original groups, where the male was
still present, to other groups. Before the movement females sometimes temporarily visited the group into which they subsequently
moved, suggesting they were able to assess social conditions during the visit. By moving, the females increased in size rank
or escaped from similar-sized female competitors in their previous groups. Although the social ranks of the moving females
in their original groups were lower than those of the resident females, the ratio of the number of females that changed sex
to the number of females surviving at the end of the study did not differ for the two types of female. Inter-group movement
of females may increase the probability of their changing sex to become a dominant male. 相似文献
The gobiid fish Trimma okinawae changes its sex bi-directionally according to its social status. Morphological changes in the urinogenital papillae (UGP) of this fish have been reported during sex change. However, there have been no detailed observations of such changes. Here, we histologically examined the UGP structure of male- and female-phase fish. UGPs of fish in female and male phase contained both oviducts and sperm ducts. Both ducts were coalesced into one duct within the posterior region of the UGP. Female-phase fish had many longitudinal folds in the hypertrophied tunica mucosa of the oviduct, which was found to be responsible for the transport of eggs and the removal of follicular cells from the oocyte. In contrast, male-phase fish had an immature oviduct and a mature sperm duct in the UGP. In the male-phase fish, the co-existence of spermatozoa and fibrillar secretions was observed in the sperm duct during spermiation. 相似文献
Reproductive ecology and function of long-term territoriality in the lefteye flounder Engyprosopon grandisquama were investigated in the southwest of Kyushu Island, Japan. Field observations of marked individuals and monthly sampling suggested that the spawning season was from June to September with a peak in June–July. During the spawning season, males maintained their mating territories, although spawning behavior was not observed in August–September. Some males stayed until the next spawning season and then acquired more mates than newly appearing males, most of which could not acquire mates. Long-term retention of territory may be more advantageous for establishing a mating territory and acquiring mates in the next spawning season. 相似文献
The gobiid fish, Trimma caudomaculatum, lives in groups. We investigated group structure, mating system and bidirectional sex change of this species. Four groups examined contained more than two males. The males were significantly larger than the females. By the observations in aquarium, the males occupied a nest and the females visited the nest for spawning. While there was no specific pair bond, the males mated with multiple females. Hence, this species establishes multi-male groups. In the experiments, four larger females had changed sex to male among 25 females. The smallest male changed to female in the group of four males. 相似文献
Suggrundus meerdervoortii (Platycephalidae) has been hypothesized to pass through four phases, thus changing sex three times: the first male, first female, second male and second female phases. In this study, gonads of males and females were constructed from developed testis with an immature ovary and only oocytes, respectively. The females in this study were significantly larger than the males. There was no female in the size range of the hypothesized first female phase. Reversed sex change among protandrous fishes has not been reported in any other studies. Thus, the specimens of the hypothesized first female phase may be different from S. meerdervoortii. Therefore, this species should be considered protandrous without reversed sex change. 相似文献
Bi-directional sex change in the deep-water gobiid fish Trimma yanagitai was examined. The gonads of all individuals consisted of ovarian and testicular elements, and an accessory gonadal structure.
In no gonads were both testicular and ovarian parts simultaneously active. Bi-directional sex changes occurred during the
rearing experiments in aquaria under conditions of which there was co-existence of two males or plural females. The sex of
individuals could be determined by their relative body size or social dominance: the largest individuals acting as male and
the remainder as female. 相似文献