Female Rhizoprionodon acutus were found to mature between 62 and 74 cm total length (L T ) whereas males matured between 63 and 71 cm L T . The L T at 50% maturity was 64Á3 cm for females and 64Á7 cm for males. Litter size varied from one to six embryos, and was positively correlated with maternal L T . Female embryos outnumbered males by a ratio of 2Á3:1. The size at birth was c. 37 cm L T . Full-term embryos and post-partum females were observed during all seasons although their occurrence was highest in spring. Spermatozoa were rarely recorded in the oviducal gland, indicating that this species does not store sperm. It was not possible to generate maturity curves for Iago omanensis but it was evident that females matured by the time they reached 35 cm and males were mature by 31 cm L T . This species displayed a clearly defined reproductive cycle with parturition occurring primarily in spring, after a gestation period of c. 1 year. Maximal embryo size was 19 cm L T while maximal litter size was 24 embryos. The oviducal gland appeared to act as a seminal receptacle and it appeared that females may utilize these stores by not mating every year.

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The anatomy of the male and female reproductive systems was investigated in the long-tailed butterfly ray Gymnura poecilura using gross observation and light microscopy. The testes are highly asymmetrical, to the extent that only the left testis is functional and the right testis is completely absent. Both of the male genital ducts are present and symmetrical, although spermatozoa only occur in the left duct. The genital ducts are straight and unconvoluted, with regular incomplete internal partitions throughout. Females do not possess a right ovary, nor do the oviducal glands exhibit distinct club and papillary zones, and the baffle zone lacks baffle plates. In all sections of the gland, the tubules display different secretory activities depending on the proximity to the gland lumen. The gland produces a thin egg membrane that encases each egg individually, while the endometrium is formed into trophonemata.

Background: It is hypothesised that being a blood-feeding ectoparasite, Argulus foliaceus (Linnaeus, 1758), uses similar mechanisms for digestion and host immune evasion to those used by other haematophagous ecdysozoa, including caligid copepods (e.g. sea louse). We recently described and characterised glands associated with the feeding appendages of A. foliaceus using histological techniques. The work described in the present study is the first undertaken with the objective of identifying and partially characterising the components secreted from these glands using a proteomic approach.Methods: Argulus foliaceus parasites were sampled from the skin of rainbow trout (Oncorhynchus mykiss), from Loch Fad on the Isle of Bute, Scotland, UK. The proteins from A. foliaceus secretory/excretory products (SEPs) were collected from the supernatant of artificial freshwater conditioned with active adult parasites (n = 5-9 per ml; n = 560 total). Proteins within the SEPs were identified and characterised using LC-ESI-MS/MS analysis. Data are available via ProteomeXchange with identifier PXD016226.

Argulus foliaceus (Linnaeus, 1758) is a member of the branchiuran family Argulidae, a group comprising parasitic "fish lice". A. foliaceus is distributed worldwide and causes major economic impacts for cultured freshwater fish globally. The work described in this study was undertaken with the objective of identifying, describing and characterising glands associated with feeding in A. foliaceus. From structural and ultrastructural microscopic studies of A. foliaceus, three types of gland were determined to be associated with the pre-oral spine and mouth tube and were suggested to be involved in feeding activities. Two of these glands, the labial glands and the proboscis glands, appeared to secrete their products via the mouth tube and a third, the spinal gland, was connected directly to the pre-oral spine. The current study confirmed that the pre-oral spine delivers active secretions from the spinal gland, which may aid in immunomodulation, while the tubular labial spines and proboscis glands openings within the mouth tube may serve to enhance the feeding process by delivering salivary components to aid pre-digestion and immune-modulate the host. The suggested functions are supported by histological and histochemical staining, coupled with fluorescent lectin-binding assays, which enabled characterisation of the carbohydrate moieties associated with these glandular tissues.