Diplostomoid digenean metacercariae have caused widescale mortalities of channel catfish, Ictalurus punctatus (Rafinesque), at aquaculture farms in Louisiana, Mississippi and Arkansas, USA. Originally, based on a tentative diagnosis, the industry considered the primary harmful agent to be an introduced species from Europe, Bolbophorus confusus (Krause, 1914), frequently reported from the American white pelican, Pelecanus erythrorhynchos Gmelin. Our group has now shown, using ITS 1-2 plus three more-conservative gene fragments, that two sympatric species of Bolbophorus exist in the American white pelican. One, B. damnificus Overstreet et Curran, 2002, infects the musculature of catfish, and the other, probably not B. confusus, does not infect catfish. However, at least four other pathogenic diplostomoids and a clinostomoid infect the catfish, and they use at least four different snail hosts, including the planorbids Planorbella trivolvis (Say) and Gyraulus parvus (Say), the physid Physella gyrina (Say) and a lymnaeid. Two metacercariae, B. damnificus and Bursacetabulus pelecanus Dronen, Tehrany et Wardle, 1999, infect the catfish and mature in the pelican; two others, Austrodiplostomum compactum (Lutz, 1928) and Hysteromorpha cf. triloba (Rudolphi, 1819), mature in cormorants; one, Diplostomum sp., matures in seagulls and at least one, Clinostomum marginatum (Rudolphi, 1819), matures in herons, egrets and other wading birds. Consequently, management of catfish ponds relative to digenean infections requires considerable biological information on the fish, bird, and snail hosts as well as the parasites.
Bentholebouria colubrosa gen. n. et sp. n. (Digenea: Opecoelidae) is described in the wenchman, Pristipomoides aquilonaris (Goode et Bean), from the eastern Gulf of Mexico, and new combinations are proposed: Bentholebouria blatta (Bray et Justine, 2009) comb. n., Bentholebouria longisaccula (Yamaguti, 1970) comb. n., Bentholebouria rooseveltiae (Yamaguti, 1970) comb. n., and Bentholebouria ulaula (Yamaguti, 1970) comb. n. The new genus is morphologically similar to Neolebouria Gibson, 1976, but with a longer cirrus sac, entire testes, a rounded posterior margin with a cleft, and an apparent restriction to the deepwater snappers. Morphologically, the new species is closest to B. blatta from Pristipomoides argyrogrammicus (Valenciennes) off New Caledonia but can be differentiated by the nature of the internal seminal vesicle (2-6 turns or loops rather than constrictions), a longer internal seminal vesicle (occupying about 65% rather than 50% of the cirrus sac), a cirrus sac that extends further into the hindbody (averaging 136% rather than 103% of the distance from the posterior margin of the ventral sucker to the ovary), and a narrower body (27% rather than 35% mean width as % of body length). A Bayesian inference analysis of partial sequence of the 28S rDNA from Neolebouria lanceolata (Price, 1934), Cainocreadium lintoni (Siddiqi et Cable, 1960), Hamacreadium mutabile Linton, 1910, Opecoeloides fimbriatus (Linton, 1910), Podocotyloides brevis Andres et Overstreet, 2013, the new species, and previously published comparable sequences from 10 opecoelid species revealed two clades. One clade includes deep-sea (≥ 200 m) and freshwater fish opecoelids + Opecoeloides Bremser in Rudolphi, 1819, and a second clade included those opecoelids from shallow-water marine, perciform fishes.
Four trypanorhynchs, Kotorella pronosoma (Stossich, 1901), Nybelinia cf. bisulcata (Linton, 1889), Nybelinia scoliodoni (Vijayalakshmi, Vijayalakshmi ct Gangadharam, 1996), and Dasyrhynchus pacificus Robinson, 1965 are reported for the first time from the Gulf, which is now known to harbour at least 34 different species. In addition to the range extension for the trypanorhynchs listed above, 21 new host records are reported involving 13 cestode species. Characters of the genus Kotorella Euzet et Radujkovic, 1989 are emended, Nybelinia narinari MaeCallum, 1917 is considered a junior synonym of Kotorella pronosoma (Stossich, 1901), and Heteronybelinia palliata (Linton, 1924) comb. n. is redescribed. The usefulness of the bulb ratio as a means to distinguish different tentaculariid species is discussed, and the importance of shallow water localities for the life cycle of trypanorhynch ccstodes is emphasised.
Psettarium anthicum sp. n. (Digenea: Sanguinicolidae) infects the myocardium and atrial wall of the cobia Rachycentron canadum (Linnaeus, 1766) (Rachycentridae) in the northern Gulf of Mexico off Mississippi, USA. It is the first member of Psettarium Goto et Ozaki, 1930 reported from other than the Indian Ocean or Pacific Ocean and the second species of the genus reported from cobia. It differs from its congeners by the combination of having posterior caeca with lateral projections appearing as thorns in lateral view and the male pore anterior to the oötype. The species of Psettarium, P. japonicum (Goto et Ozaki, 1929) (type species), P. tropicum Manter, 1940, P. sebastodorum Holmes, 1971, P. rachycentri (Lebedev et Parukhin, 1972) comb. n. (syn. Psettarioides rachycentri Lebedev et Parukhin, 1972) and P. anthicum sp. n., differ from other sanguinicolids by the combination of having an elongate body with a sinistral posterolateral protuberance, minute, straight tegumental body spines in ventrolateral transverse rows, posterior caeca greater than seven time the anterior caeca length, the oötype near the posterior end of the body, a uterus primarily between the ovary and oötype and an oviduct and vitelline duct extending posteriad primarily between the uterus and dextral body margin. We emend Psettarium and provide a diagnostic key to the species. Psettarioides is regarded as a junior synonym of Psettarium because herein we return its type species, P. tropicum, to Psettarium. Regarding the three other sanguinicolids formerly of Psettarioides, we suspect that P. pseudupenei Lebedev et Parukhin, 1972 belongs to Psettarium but include it only tentatively pending an examination of type or other material; we tentatively place P. kurochkini Parukhin, 1976 in Cardicola Short, 1952; and we designate P. grandis (Lebedev et Mamaev, 1968) as incertae sedis pending examination of type or other appropriate material.