The presently reported study provides a detailed morphological description of the female and the male of a new species of the genus Parabrachiella-Parabrachiella jarai sp. nov. The parasites were sampled from marine fish, silver sillago, Sillago sihama (Perciformes: Sillaginidae), captured in Malaysia in 1994 and Hong Kong in 1995. The new species bears some resemblance to Parabrachiella lata (Song et Chen, 1976) but differs from it in details of second antenna, mandible, and maxilliped. The genus Parabrachiella currently covers 67 species including those recently transferred from Neobrachiella Kabata, 1979. An amended generic diagnosis is proposed for Parabrachiella and Thysanote. Some members of Parabrachiella are herewith transferred to Thysanote and some Thysanote are now placed in Parabrachiella.
In view of recent studies, we suggest that the term "preadult" should not be used in scientific reports on Copepoda parasitic on fishes as having no explicit meaning or further justification. Consequently, the term "chalimus" with its use currently restricted in the Caligidae to at most two instars in the life cycles of species of Lepeophtheirus, also becomes redundant. In our new understanding, both the chalimus and preadult stages should be referred to as the respective copepodid stages (II through V, in integrative terminology). The terminology for the caligid copepod life cycle thereby becomes consistent with that for the homologous stages of other podoplean copepods. We see no justification for keeping "chalimus" and "preadult" even as purely practical terms. To justify this reinterpretation, we comprehensively summarize and reinterpret the patterns of instar succession reported in previous studies on the ontogeny of caligid copepods, with special attention to the frontal filament. Key concepts are illustrated in diagrams. We conclude that, using the new integrative terminology, copepods of the family Caligidae have the following stages in their life cycles: nauplius I, nauplius II (both free-living), copepodid I (infective), copepodid II (chalimus 1), copepodid III (chalimus 2), copepodid IV (chalimus 3/preadult 1), copepodid V (chalimus 4/preadult 2), and adult (parasitic). With this admittedly polemical paper, we hope to spark a discussion about this terminological problem.
Both sexes of Brachiella malayensis n. sp. are described on the basis of specimens found in the nostrils of narrow-barred Spanish mackerel Scomberomorus commerson (Lacepède) collected off Besut, Malaysia. The female of this species closely resembles those of B. magna Kabata, 1968 and B. cybii Pillai, Prabha et Balaraman, 1982 but is distinguishable mainly by the body size and the proportions of the cephalosome, posterior processes and caudal rami. While examining the male, we noticed a systematic inconsistency in some lernaeopodid genera. The genus Brachiella Cuvier, 1830, represented by its type-species Brachiella thynni Cuvier, 1830, and two monotypic genera Charopinopsis Yamaguti, 1963 and Eobrachiella Ho et Do, 1984, represented by Charopinopsis quaternia (Wilson, 1935) and Eobrachiella elegans (Richiardi, 1880), respectively, share distinct synapomorphies in the embracing (vs. pinching) elongate male maxilliped and the female trunk with a pair of long, cylindrical ventroposterior processes (in addition to a pair of modified caudal rami), both of which are involved in their unique reproductive strategy. The latter two genera are herewith relegated to junior synonyms of Brachiella.