Studies on the reproductive cycle, sexual maturation, and spawning of Haliotidae species have been conducted to accumulate data on basic biology, resource management, and culture technology development (Webber & Giese, 1969; Sobhon et al., 1999; Najmudeen & Victor, 2004; Visser-Roux, 2011).

This study was performed to obtain information on the sex ratio, spawning period, and size at sexual maturity for fishery management of the largehead hairtail Trichiurus japonicus in Korean waters. The overall sex ratio (female, F; male, M) was 1:0.46 (n = 1274 females:589 males, 68.4% female) and as fish increased in length, the proportion of females increased. The oocyte development pattern was group-synchronous development, for which oocyte groups at different stages can be identified within the same ovary. The average gonadosomatic index (GSI) showed two peaks in June (3.03) and August (3.10) in females and in May (1.81) and September (2.24) in males. The median value of GSI showed two peaks in May (2.65F, 1.78M) and September (2.55F, 1.87M) for both females and males. As a result of analyzing the GSI and the monthly gonadal developmental stages, the main spawning season was estimated to be bi-annual (May–June and September–October). The anal length of fish at 50% sexual maturity was analyzed using a logistic regression model and was determined to be 16.38 cm (female) and 18.31 cm (male).

In general, the determination of animal sex is based on their morphological sex. Sex of bivalves can be categorized as either gonochoristic or hermaphroditic, whereas hermaphrodites can be described as either simultaneous or sequential (Coe, 1943; Heller, 1993; Yusa, 2007). Sequential hermaphrodites undergo sex changes during their life cycle, and their morphological sex is expressed differently according to the life cycle stage. The identification of sequential hermaphroditism requires direct evidence of sex change (Coe, 1943; Lee et al., 2013, 2014). However, since obtaining direct evidence requires considerable time and effort, an indirect method is used to analyze the change in sex ratio according to age or size within the same population (Galtsoff, 1937; Guo et al., 1998; Eversole, 2001; Park et al., 2012). The purpose of this study was to analyze the sex ratio of the mussel Mytilus coruscus, which is known to be gonochoristic (Wi et al., 2003), to thus describe its sex changes and sex.

The present study describes the differentiation process of male germ cells in Octopus vulgaris, the morphology of sperm in the testis and spermatophore, and the sperm released after the spermatophoric reaction. During spermatogenesis, the male sperm cell gradually elongates from a round shape, with cytoplasm shifting toward the head and the acrosome forming. Additionally, in the spermatid stage, the flagellum develops within the posterior nuclear channel and extends outside the cytoplasm. The sperm is composed of a head and a tail. The head is approximately 17.9 μm long and consists of a highly electron-dense nucleus and a helical acrosome. The tail is divided into three parts: the mid-piece, principal-piece, and end-piece. The mid-piece forms a mitochondrial sheath with 7–8 mitochondria surrounding a “9+2” axoneme. The principal-piece is composed of an axoneme, outer dense fibers, and fibrous sheath, while the end piece lacks outer dense fibers or fibrous sheath. The sperm in the testis and spermatophore, and the sperm released after the spermatophoric reaction have the same structure. However, in the sperm located in the testis and spermatophore, the structure of the acrosome is unclear due to the presence of cytoplasm in the head. In contrast, sperm released after the spermatophoric reaction lack their cytoplasm, revealing the helical acrosome. This unique sperm morphology, adapted for internal fertilization, is thought to be advantageous for fertilization and long-term storage within the female reproductive system.

This study was performed to obtain information on the basic reproductive ecology and biological resource management of Buccinum osagawai. Samples were collected from August 2018 to October 2019 with a drum-shaped net at a depth of 150–250 m along the continental shelf in Jumunjin, on the east coast of Korea. The species showed gonochorism and a lack of external sexual dimorphism. The overall sex ratio (F:M) was 1:1.2 (n = 549, F = 250, M = 299); as the size of the individuals increased, the proportion of males tended to decrease. The development pattern of the oocyte was synchronous, in which a dominant group of oocytes was identified within the same ovary. The size of the ripe oocyte was 82.3 (±22.6) × 125.5 (±22.0) μm. The spermatocyte development pattern was group-synchronous, in which multiple stages of germ cell populations were simultaneously identified within the same spermatogenic acinus. The gonad index (GI) for both males and females showed the highest value during June, after which it decreased sharply, and after August it was below 2.0. The main spawning season was from June to July, and the GI and stages of gonadal development did not show a pattern of seasonal changes. The main gonadal active season was from May to July, and both male and female gonadal development and maturation took place over a short period, whereas the recovery period after spawning was longer. At least 60.5% of the group, considering both males and females, showed maturity at 50.1 mm SH or more. Furthermore, the size of 50% group maturity was shown at approximately 50.0 mm SH.