Unusual opecoelids from Red Sea triggerfishes with special reference to characteristic concepts of the Opistholebetinae Fukui, 1929 (Digenea: Opecoelidae).

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.

Re-examination of the phylogenetic relationships within the Gyliauchenidae Fukui, 1929 (Digenea) based on morphological and molecular evidence with a proposal for Paragyliaucheninae n. subfam. and a description of Flagellotrema convolutum Ozaki, 1936.

Flagellotrema convolutum Ozaki, 1936 was found parasitising the intestine of two new host fish species, the Indian sail-fin surgeonfish, Zebrasoma desjardinii (Bennett) (Acanthuridae), and the Picasso triggerfish, Rhinecanthus assasi (Forsskål) (Balistidae), from the northern Red Sea off Egypt. Another description of this species is provided with detailed morphological observations made of the genital systems. Using newly acquired molecular data from the D1-D3 regions of 28S rDNA, the phylogenetic relationships of subfamilies and genera within the Gyliauchenidae Fukui, 1929 are elucidated with morphological support. The Petalocotylinae Ozaki, 1934 and the Robphildollfusiinae Paggi & Orecchia, 1963 are recognized as valid subfamilies within the Gyliauchenidae. The Apharyngogyliaucheninae Yamaguti, 1942 and the Ichthyotreminae Caballero & Bravo-Hollis, 1952 remain junior synonyms of the Gyliaucheninae Fukui, 1929. Based on its unique position relative to all gyliauchenid subfamilies and its distinct separation from all other gyliauchenine genera, the Paragyliaucheninae n. subfam. is erected to contain Paragyliauchen Yamaguti, 1934. Paragyliauchen differs from all other gyliauchenine genera by having a pharynx differentiated into two, well-developed muscular regions: an anterior region composed of a ring with indented projections anteriorly and a posterior region that is ellipsoidal or barrel-shaped. Modified and/or new keys to the four subfamilies we recognize within the Gyliauchenidae as well as the genera within each subfamily are presented, and we discuss the evolutionary development and etymology of the unique anatomy of the anterior of gyliauchenids.

Pelopscreadium aegyptense n. gen., n. sp. and Pelopscreadium spongiosum (Bray & Cribb, 1998) n. comb., (Digenea: Lepocreadiidae), each from disjunct populations of the Yellow boxfish, Ostracion cubicus Linnaeus (Ostraciidae).

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.