Telotha henselii (Von Martens, 1869) attached to the carapace of the prawn, Palaemonetes carteri (Gordon, 1935) laterally on the cephalothorax near the branchial chamber. Scale bar = 5 mm. 

Telotha henselii (Von Martens, 1869) attached to the carapace of the prawn, Palaemonetes carteri (Gordon, 1935) laterally on the cephalothorax near the branchial chamber. Scale bar = 5 mm. 

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Telotha henselii (Crustacea, Isopoda, Cymothoidae) is reported for the first time from the branchial region of the shell of the shrimp Palaemonetes carteri (Crustacea, Decapoda, Palaemonidae), collected in the Amazon River, municipality of Itacoatiara, Amazon, Brazil. T. henselii parasitized 4.4% of the P. carteri collected. The parasitic specifici...

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... width 1.8-2 mm. Both isopods were attached to the carapace of the prawn, laterally on the cephalothorax near the branchial chamber (fig. 3). From Brazil, T . henselii has been recorded from two localities in southern Brazil (Von Martens, 1869; Schioedte & Meinert, 1884; Lemos de Castro & Gomes Corrêa, 1982; Alberto et al., 2001), two in the western-central part (Lemos de Castro, 1985), and now also parasitizing prawns in northern Brazil (present study) (see table I). According to Trilles (1994) and Thatcher (2006), three species belonging to the genus Telotha , Telotha henselii , T. lunaris Schioedte & Meinert, 1884, and T. silurii Szidat & Schubart, 1959 have been reported from Brazilian fish. Among these, only one, i.e., T. henselii , has also been reported parasitizing palaemonid prawns (Lemos de Castro & Gomes Corrêa, 1982; Lemos de Castro, 1985; Alberto et al., 2001). Telotha lunaris was only collected from the branchial cavity of Apteronotus ( = Stenarchus ) brasiliensis (Reinhardt, 1852) (Teleostei, Apteronotidae), whereas T. silurii has only been reported on Iheringichthys labrosus (Lütken, 1874) (Teleostei, Pimelodidae). The great variety of hosts parasitized by T. henselii in both life phases shows, that this species has low host specificity. ...

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Thesis
In crustaceans, both protandric and protogynic hermaphroditism may have been developed independently several times and the Isopoda is the only crustacean order in which both protandrous and protogynous species occur (Brook et al., 1994). The dominant pattern of sequential hermaphroditism is reported to be protandry which is exhibited by hippolytids, crayfishes (Parastacidae) and isopods (Brook et al., 1994; Almeida and Buckup, 1997). In Isopoda, protandrous sex change occurs primarily within the parasitic groups such as epicarids and cymothoids. An interesting case of protandrous hermaphroditism has been reported in the cymothoid, Anilocra frontalis, infesting the fishes, Labrus bergylta and L. maculatus; the male parasitic member which remains alone on a fish, starts functioning as a female. But if another male settles besides the female, it (the new male) remains in its male stage until the female dies or is experimentally removed (Legrand, 1952; Juchault, 1966). Available reports showed that the reproductive cycle and breeding pattern of the parasitic isopod is closely associated to the life cycle of the host (Leonardos and Trilles, 2004). In Glossobius hemiramphi, the reproduction is prolonged throughout the year (Bakenhaster et al., 2006). According to Adlard and Lester (1995), the female cymothoid, Anilocra pomacentri can produce multiple broods. Reproduction of Mothocya bohlkeorum and M. epimerica is repeated at intervals of about 2 months and produces multiple broods (Williams and Williams, 1982; Bello et al., 1997). The number of eggs/embryos/larvae per brood is not known for majority of cymothoid species. According to Marks et al. (1996), cymothoids produce a small number of eggs per female. M. epimerica and Ryukyua globosa produce an average number of 164 and 362 eggs respectively (Williams and Williams, 1994; Bello et al., 1997). Several morphological and anatomical studies have demonstrated that the reproductive system in crustaceans varies in structure from species to species (Anilkumar, 1980; Diesel, 1989; Chow et al., 1991; Sudha, 1992; Suganthi, 1996; Anilkumar et al., 1999; Baby Joseph, 2007). However, most of earlier investigations concern decapods. In isopods, little work has been focused on the structure of reproductive system. In free living, non-hermaphroditic isopod, Saduria entomon, the spermatogenesis in the testicular tubules is not synchronized and in each of the tubules, germ cells are at different stages of maturation. The developing germ cells in the testis have been shown to associate with the somatic cells or accessory cells (Hryniewiecka-Szyfter and Tyczewska, 1991). Ultrastructural investigations in other free living isopods such as Oniscus asellus (Reger and Fain-Maurel, 1973) and Armadillidium vulgare (Itaya, 1979) suggest that accessory cells produce the extracellular tubules surrounding bundles of spermatozoa in spermatophores. Free living isopods have been shown to have a particular type of aflagellate, immotile spermatozoon, made up of two linear associated components: the cell body containing a long ribbon-like nucleus, above which an acrosomal complex is present, and a long flexible tail with a paracrystalline structure (Cotelli et al., 1976; Reger et al., 1979). In the females of S. entomon and Asellus aquaticus, the ovulatory canal is modified in such a way for the formation of spermatic reservoir (Hryniewiecka-Szyfter and Babula, 1995; Erkan, 1998). Nevertheless, cymothoids are reported to be protandrically hermaphroditic, no detailed study is available on the organization of reproductive system associated with the form of hermaphroditism in this group. The knowledge on the structure of reproductive/sexual system at different stages of its adult life is necessary to describe the mode of hermaphroditic life exhibited by the species. Keeping this in mind, the present chapter is devoted to study the reproductive biology of the candidate cymothoid species, M. renardi by giving thrust to the following aspects (i) organization of the reproductive system at morphological, histological and ultrastructural levels, (ii) correlation between the ovarian cycle and brood cycle and (iii) correlation between ovarian cycle and moult cycle.