Modified and/or new keys to the four subfamilies now recognized within the Megaperidae Manter, 1934 n. comb. (Syn. Apocreadiidae Skrjabin, 1942) as well as the genera within each subfamily are presented. Two new genera, Paraschistorchis n. gen. and Plesioschistorchis n. gen., both within the Schistorchiinae Yamaguti, 1942, are erected and keys are provided to the species considered in both new genera-distinguished by possessing caeca that end either in separate ani or blindly. Plesioschistorchis callyodontis (Yamaguti, 1942) n. comb. and Plesioschistorchis haridis (Nagaty, 1957) n. comb. are re-described from new material collected from the common parrotfish, Scarus psittacus Forsskål (Perciformes: Scaridae), inhabiting the Red Sea off Egypt; S. psittacus represents a new host record for both species. The taxonomic status of Schistorchis sensu stricto Lühe, 1906 is examined and revised, a key to the four species we consider in this genus offered, and the monotypic genus Megacreadium Nagaty, 1956 declared a junior synonym of Schistorchis. Members of Schistorchis sensu stricto possess a unique "complex" (i.e. highly cellular/glandular) instead of "simple" (i.e. entirely muscular) type of oral sucker that is quite large in relation to body size; an elongate, somewhat sub-rectangular-shaped body; 5+ testes arranged in at least two rows; caeca that open via separate ani; a long post-testicular region; a median genital pore either at the anterior margin of or just anterior to the ventral sucker; and species of Schistorchis sensu stricto parasitize the intestine of marine fish within the Order Tetraodontiformes Berg. With the revision of this genus, we re-describe Schistorchis carneus Lühe, 1906 from the lower and mid-intestine of the white-spotted puffer, Arothron hispidus (Linnaeus) (Tetraodontiformes: Tetraodontidae), collected in the Red Sea off Egypt. Finally, a plea is made for further study of the Megaperidae n. comb. focusing, in particular, on the following: (1) obtaining new type/voucher materials of Plesioschistorchis manteri (Gupta & Tandon, 1984) n. comb. and Schistorchis paruchini Kurochkin, 1974; (2) elucidating the life histories (i.e. intermediate hosts) of members of the Postporinae Yamaguti, 1958 and Schistorchiinae; and (3) generating DNA sequence data for more species of megaperids to help future workers produce increasingly accurate taxonomic classifications that better reflect phylogenetic relationships within this ecologically diverse group of digeneans.
Three digeneans belonging to the Opecoelidae are reported and described from triggerfishes (Tetraodontiformes: Balistidae) collected in the northern Red Sea off Egypt. Both Macvicaria longicirrata (Manter, 1963) Aken-Ova, Cribb & Bray, 2008 and Neopycnadena tendu (Bray & Justine, 2007) n. comb. were recovered from the intestine of the titan triggerfish, Balistoides viridescens (Bloch & Schneider)—each represents a new host record—and Gaevskajatrema balistes n. sp. was found parasitizing the lower intestine of the Picasso triggerfish, Rhinecanthus assasi (Forsskål). We continue to support synonymy of Gaevskajatrema ponticum (Koval, 1966) Machkevsky, 1990 with Gaevskajatrema perezi (Mathias, 1926) Gibson & Bray, 1982, not as a differentiated species. We adopt the restricted posterior extension of the ceca and vitellarium to the testicular zone, without extension of either into the post-testicular space, as diagnostic in distinguishing Gaevskajatrema. Gaevskajatrema balistes n. sp. differs from G. perezi based on its substantially smaller body size with fewer eggs, a longer cirrus-pouch reaching ovarian level and it parasitizes a distinct host group from a structurally and ecologically different ecosystem. Neopycnadena n. gen. is erected for Pseudopycnadena tendu Bray & Justine 2007 based on its possessing a large broadly oval cirrus-pouch with a massive field of prostatic cells occupying the entire volume of the cirrus-pouch, a wide, cup-shaped and thick-walled ejaculatory duct, distinct dorsal position of the excretory pore, the bifurcal dextral position of the genital pore, its report from a distinct host group and distant locality and its phylogenetic uniqueness compared with Pseudopycnadena fischthali Saad-Fares & Maillard 1986. Neopycnadena n. gen. is ecologically similar to opistholebetines in their life-cycles and morphology; however, phylogenetically separate from opistholebetines as well as from the Polypipapiliotrematinae Martin, Cutmore & Cribb in Martin, Sasal, Cutmore, Ward, Aeby & Cribb, 2018 and members of Clade [C] of Martin and colleagues, thus we conclude that Neopycnadena n. gen. is unique. Neopycnadeninae n. subfam. is proposed to accommodate Neopycnadena n. gen. We consider that the probable characterization of tetraodontiform specialist taxa (as indicated by the presence of a muscular post-oral ring) and the specificity of the Opistholebetinae Fukui, 1929 sensu stricto with a tetraodontiform host are no longer reliable characters differentiating Gaevskajatrema and Macvicaria Gibson & Bray, 1982. The nature of the post-oral structure is discussed and it is adopted to be a diagnostic feature at the generic level among taxa of the Opistholebetinae sensu latu. It is concluded that the expanded concept of the Opistholebetinae is more supported than the restricted one, Birendralebes Srivastava & Ghosh, 1972 remains incertae sedis within the Opecoelidae Ozaki, 1925 rather than in the Opistholebetinae, and we provide a generic key to the Opistholebetinae.
Species of Astiotrema Looss, 1900 (sensu lato) infect a wide range of fishes, amphibians and reptilians. They also possess a considerably wide spectrum of morphological features. Several species were recognized for variable, confusing, overlapping and unspecialized morphological characters rather than for unique distinguishing features, causing continuing dispute around the validity of several species. Following comprehensive review, a revised restricted concept of Astiotrema is proposed including a morphologically strict definition. Both Tremiorchis Mehra & Negi, 1926 and Astioglossimetra Bilqees, Khatoon & Khan, 2002 are synonymized with Astiotrema (sensu stricto). Several nominal species are synonymized, others are excluded and characters for each recognized species are presented and explained. Only eight species are recognized: Astiotrema cyclemysi Siddiqi, 1965, Astiotrema emydis Ejsmont, 1930, Astiotrema fotedari Dhar, 1977, Astiotrema impletum (Looss, 1899) Looss, 1900, Astiotrema karachiensis (Bilqees, Khatoon & Khan, 2002) n. comb., Astiotrema odhneri Bhalerao, 1936, Astiotrema ranarum (Mehra & Negi, 1926) Fotedar, 1971 and Astiotrema reniferum (Looss, 1898) Looss, 1900. A key to the species of Astiotrema (sensu stricto) is presented, a comprehensive list of all host-locality records is included and host-parasite specificity is elucidated.
Bianium spongiosum Bray & Cribb, 1998 (Lepocreadiidae), described from the yellow boxfish, Ostracion cubicus Linnaeus (Ostraciidae), off Lizard Island, Queensland, Australia, possesses a combination of the following three morphological features which distinguishes it from all the other species currently assigned to the genus: (1) large internal patches of large cells forming sponge-like pads we have termed "pelops"("pelop" sing.) laterally in the forebody extending from near the anterior extremity to about the level of the intestinal bifurcation rather than possessing a scoop; (2) ceca that reach to near the posterior extremity where they end blindly without ani; and (3) a vitellarium which is present laterally but not dorsal to the ceca. Based on this we propose the erection of Pelopscreadium n. gen. (Lepocreadiidae) with the assignment of B. spongiosum to this new genus as the type-species, Pelopscreadium spongiosum (Bray & Cribb, 1998) n. comb. Pelopscreadium aegyptense n. sp., also from the yellow boxfish but from the Red Sea off Sharm El-Naga, Egypt, is described as the second member of the new genus because it shares these three characteristics with P. spongiosum.
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