Of the 95 known families of Isopoda only a few are parasitic namely, Bopyridae, Cryptoniscidae, Cymothoidae, Dajidae, Entoniscidae, Gnathiidae and Tridentellidae. Representatives from the family Cymothoidae are obligate parasites of both marine and freshwater fishes and there are currently 40 recognised cymothoid genera worldwide. These isopods are large (>6 mm) parasites, thus easy to observe and collect, yet many aspects of their biodiversity and biology are still unknown. They are widely distributed around the world and occur in many different habitats, but mostly in shallow waters in tropical or subtropical areas. A number of adaptations to an obligatory parasitic existence have been observed, such as the body shape, which is influenced by the attachment site on the host. Cymothoids generally have a long, slender body tapering towards the ends and the efficient contour of the body offers minimum resistance to the water flow and can withstand the forces of this particular habitat. Other adaptations to this lifestyle include small sensory antennae and eyes; a very heavily thickened and calcified cuticle for protection; and sharply curved hooks on the ends of the pereopods which allows these parasites to attach to the host. Most cymothoids are highly site and host specific. Some of these parasitic cymothoids have been reported to parasitise the same host fish species for over 100 years, showing this species specificity. The site of attachment on the host (gills, mouth, external surfaces or inside the host flesh) can also be genus or species specific. This paper aims to provide a summary of our current knowledge of cymothoid biodiversity and will highlight their history of discovery, morphology, relationships and classification, taxonomic diversity and ecology.

Based on 18S-rDNA sequences of 97 isopods including 18 Sphaeromatidea, we show Sphaeromatidae, Valvifera, Serolidae, and Ancinidae is a well supported clade. The within clade relationships of these taxa are not as definitively demonstrated because taxon sampling for some groups is still limited. In our analyses the Sphaeromatidae are shown to be unequivocally monophyletic. This is contrary to the morphology-based analysis by A. Brandt and G. Poore in 2003, which included only five Sphaeromatidae and found the family to be paraphyletic. The Ancinidae are also upheld, and the Valvifera is the sister taxon to Serolidae. Surprisingly Plakarthrium (Plakarthiidae) is nested within the Sphaeromatidae in most analyses. We point out short-comings in our sampling and suggest areas which would benefit from better sampling. We also review the long and convoluted nomenclatural history of the Sphaeromatidea, Sphaeromatoidea, and Sphaeromatidae.

The genus Ceratothoa Dana, 1852, is revised for Australian waters. Ceratothoa is represented in Australia by nine species, including two new species: Ceratothoa barracuda sp. nov. described from Cairns and Ceratothoa globulus sp. nov. described from Lord Howe Island. Ceratothoa imbricata Fabricius, 1775 is redescribed, with Ceratothoa trillesi (Avdeev, 1979) and Ceratothoa huttoni Filhol, 1885 placed into junior synonymy; the preferred hosts are species of the genus Trachurus (Carangidae). Ceratothoa banksii (Leach, 1818) is validated and brought out of synonymy with Ceratothoa imbricata; host species are from the families Kyphosidae, Scombridae, Latridae, Carangidae, Mugilidae, Salmonidae, Scatophagidae, Pomatomidae and Hemiramphidae. Species excluded from the Australian fauna are Ceratothoa trigonocephala (Leach, 1818) with an unknown host identity and type locality; and Ceratothoa lineata Miers, 1876a, that here is transferred to the genus Mothocya Costa, 1851, with Mothocya ihi Bruce, 1986 placed into junior synonymy. Ceratothoa contracta (Miers, 1880), the New Zealand Ceratothoa novaezelandiae Filhol, 1885 and the East Pacific Ceratothoa gaudichaudii (Milne Edwards, 1840) are regarded here as species inquirenda. A key to the Australian species of Ceratothoa is presented.

Lepidocharontidae Galassi & Bruce, fam. n. is erected, containing Lepidocharon Galassi & Bruce, gen. n. and two genera transferred from the family Microparasellidae Karaman, 1934: Microcharon Karaman, 1934 and Janinella Albuquerque, Boulanouar & Coineau, 2014. The genus Angeliera Chappuis & Delamare Deboutteville, 1952 is placed as genus incertae sedis in this family. The Lepidocharontidae is characterised by having rectangular or trapezoidal somites in dorsal view, a single free pleonite, a tendency to reduction of the coxal plates, and the unique uropodal morphology of a large and long uropodal protopod on which the slender uropodal exopod articulates separately and anteriorly to the endopod. Lepidocharon Galassi & Bruce, gen. n. has a 6-segmented antennula, a well-developed antennal scale (rudimentary exopod), long and slender pereiopods 1–7 directed outwards, coxal plates rudimentary, incorporated to the lateral side of the sternites, not discernible in dorsal view, the single pleonite narrower than pereionite 7, scale-like elements bordering the proximal part of male pleopod 1 on posterior side, and stylet-guiding grooves of male pleopod 1 which run parallel to the outer lateral margins of the same pleopod. Lepidocharon priapus Galassi & Bruce, sp. n., type species for the genus, and Lepidocharon lizardensis Galassi & Bruce, sp. n. are described from Lizard Island, northern Great Barrier Reef. The most similar genus is Microcharon, both genera sharing the same general organization of the male pleopods 1 and 2, topology and architecture of the stylet-guiding groove of male pleopod 1, morphology of female operculum, presence of 2 robust claws of different lengths on pereiopodal dactylus 1–7, not sexually dimorphic. Lepidocharon gen. n. differs from Microcharon in the shape of the pereionites, very reduced coxal plates, the presence of imbricate scale-like elements bordering the proximal postero-lateral margins of the male pleopod 1, and the topology of the pereiopods, which are ventro-laterally inserted and directed outwards in Lepidocharon gen. n. and dorso-laterally inserted and directed ventrally in Microcharon. Lepidocharon shares with the genus Janinella the morphology of the tergites and the reduced lacinia mobilis of the left mandible, but differs significantly from Janinella in having a well-developed antennal scale, very reduced coxal plates also in females bearing oostegites, the general morphology and spatial arrangement of the stylet-guiding groove of male pleopod 1 and the possession of a 6-segmented antennula. The family Microparasellidae is redefined as monotypic, the only genus being Microparasellus Karaman, 1933.

Eleven species including six new species of Gnathiidae (Crustacea, Isopoda, Cymothoida) are reported from the Heron Island and Wistari Reef, Capricorn Group, southern Great Barrier Reef: Elaphognathia queenslandica sp. nov., Gnathia acrorudus sp. nov., Gnathia capricornica sp. nov., Gnathia carinodenta sp. nov., Gnathia formosa sp. nov. and Gnathia glaucostega sp. nov. Gnathia cornuta Holdich & Harrison, 1980 and Gnathia grutterae Ferreira, Smit & Davies, 2010 are for the first time reported from Heron Island and new records from Heron Island are provided for Gnathia biorbis Holdich & Harrison, 1980, Gnathia variobranchia Holdich & Harrison, 1980, and Gnathia wistari Svavarsson & Bruce, 2012.

The genus Cymothoa Fabricius, 1793 is revised for Australian waters. Cymothoa hermani Hadfield, Bruce & Smit, 2011, previously known from Tanzania on the host Selar crumenophthalmus (Bloch, 1793) is new to Australian waters. Cymothoa carangi Avdeev, 1979; Cymothoa epimerica Avdeev, 1979; Cymothoa parupenei Avdeev, 1979; Cymothoa propria Avdeev, 1979; Cymothoa rotunda Avdeev, 1979 and Cymothoa pulchrum Lanchester, 1902 are redescribed. Cymothoa curta Schioedte & Meinert, 1884, first described from the host Anableps anableps (Linnaeus, 1758); and Cymothoa plebeia Schioedte & Meinert, 1884, first described from Cape Verde; are redescribed and excluded from the Australian fauna. Cymothoa limbata Schioedte & Meinert, 1884 is placed into junior synonymy with Cymothoa eremita (Brünnich, 1783). A key to the Australian species of Cymothoa is presented.