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Abstract. Laboratory work was conducted to elucidate the life cycle of the South African gnathiid isopod, Gnathia africana Barnard, 1914. The natural fish hosts of this temporary parasite, the super klipfish Clinus superciliosus (Linnaeus, 1758), were exposed to gnathiid larvae in the laboratory. It was found that G. africana has three larval stages, consisting of three unfed (zuphea) and three fed (praniza) stages. First-, second-and third-stage zuphea larvae took an average of 2 h 18 min, 2 h 43 min and 10 h 8 min respectively to complete their feeding and the first-and second-stage praniza moulted at 8 and 10 days respectively into the next zuphea stage. Three to six days after its last blood meal, the sex of the third and final praniza stage could be determined by the presence of either a testis or two ovaries in the dorsal pereon. Male larvae moulted into adult males between 8 and 10 days post feeding. Female larvae moulted at approximately 17 days into adult females. The life cycle and ecology of members of the family Gnathiidae have intrigued scientists for more than two centuries. Even now the information available on these aspects of gnathiid biology is scanty. To the authors' knowledge the life cycle of only the following six of the more than 170 described gnathiid species has been researched in any detail: Gnathia maxillaris (Montagu,

Abstract. Haemogregarina bigemina Laveran et Mesnil, 1901 was examined in marine fishes and the gnathiid isopod, Gnathia africana Barnard, 1914 in South Africa. Its development in fishes was similar to that described previously for this species. Gnathiids taken from fishes with H. bigemina, and prepared sequentially over 28 days post feeding (d.p.f.), contained stages of syzygy, immature and mature oocysts, sporozoites and merozoites of at least three types. Sporozoites, often five in number, formed from each oocyst from 9 d.p.f. First-generation merozoites appeared in small numbers at 11 d.p.f., arising from small, rounded meronts. Mature, second-generation merozoites appeared in large clusters within gut tissue at 18 d.p.f. They were presumed to arise from fan-shaped meronts, first observed at 11 d.p.f. Third-generation merozoites were the shortest, and resulted from binary fission of meronts, derived from second-generation merozoites. Gnathiids taken from sponges within rock pools contained only gamonts and immature oocysts. It is concluded that the development of H. bigemina in its arthropod host illustrates an affinity with Hemolivia and one species of Hepatozoon. However, the absence of sporokinetes and sporocysts also distances it from these genera, and from Karyolysus. Furthermore, H. bigemina produces fewer sporozoites than Cyrilia and Desseria, although, as in Desseria, Haemogregarina (sensu stricto) and Babesiosoma, post-sporogonic production of merozoites occurs in the invertebrate host. The presence of intraerythrocytic binary fission in its fish host means that H. bigemina is not a Desseria. Overall it most closely resembles Haemogregarina (sensu stricto) in its development, although the match is not exact.

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