AIR SAC TREMATODES (CYCLOCOELIDAE STOSSICH, 1902) INFECTING BIRDS IN ZOOLOGICAL INSTITUTIONS IN THE UNITED STATES.

Air sac trematodes (Digenea: Cyclocoelidae) were detected in 23 avian species from eight aviaries in the United States. Most of the infected host species were passeriform birds, but a few species in other orders also were infected. Four species of adult flukes were encountered: Circumvitellatrema momota, Morishitium sp., Psophiatrema greineri, and Szidatitrema yamagutii. Findings from retrospective review of medical records, necropsy records, and author observations are presented. Potential terrestrial snail intermediate hosts were collected from three indoor aviaries. A high prevalence (47%) of larval trematode infections was demonstrated in one species of nonnative snail (Prosopeas achatinacea); one larva was isolated and matched to the adult species (C. momota) from birds using PCR. Problems with introducing potentially infected wild-caught birds into aviaries, and exchanging captive individuals between aviaries where they potentially may carry infections, are discussed.

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.

Detection and Management of Air Sac Trematodes (Szidatitrema Species) in Captive Multispecies Avian Exhibits.

From 2 exhibits in a zoological collection, 2 juvenile fairy bluebirds ( Irena puella ) and 1 adult blue-grey tanager (Thraupis episcopus) died within 3 months of one another. The cause of death was attributed to air sac trematodes, which were identified as Szidatitrema species based on morphology of adult trematodes and miracidia isolated from a snail intermediate host. To determine the extent of trematodiasis in the collection, individual exhibits within the same building as the original presenting cases were assessed, with birds representing 27 avian species from 9 orders. Sampling consisted of individual (n = 244) and pooled same-species group (n = 193) fecal examinations, and for some individuals, and tracheal swab (n = 106), resulting in a total of 543 samples. In addition, tracheal swabs were performed on 14 birds for comparative cytology, but no parasites were found. Flukes were positively identified in 4 tracheal swab samples (4%), 37 individual fecal samples (15%), and 52 of the group fecal samples (27%). When results of the swab method were compared with those of fecal examination, fecal testing was significantly associated (P < .001) with positive results. Based on these results, a screening process was instituted of 3- or 4-day combined fecal samples evaluated by both sedimentation and flotation techniques 2 weeks before outgoing shipments or intrazoo transfers of birds housed in exhibits known to have snail populations. Snail control methods also were initiated in all exhibits. Treatment with praziquantel was carried out on a case-by-case basis, and included oral, parenteral, and nebulized administration. Although control measures were expected to manage the infection and reduce distribution of the parasite to other collections, complete eradication of trematodes in the population is unlikely.

Keys to the species of Neolebouria Gibson, 1976 (Digenea: Opecoelidae: Plagioporinae), with a redescription of Neolebouria truncata (Linton, 1940).

Three keys to the species of Neolebouria Gibson, 1976, representing three body types, are provided based on the location of the genital pore relative to the intestinal bifurcation. These are: the lanceolata body type, where the genital pore is clearly prebifurcal; the diacopae body type, where the genital pore is located at or near the level of the intestinal bifurcation; and the maorum body type, where the genital pore is clearly postbifurcal. Fifteen species were assigned to the lanceolata body type; eight species to the diacopae body type; and four species to the maorum body type. Neolebouria truncata (Linton, 1940) is redescribed and N. georgiensis Gibson, 1976 is reinstated as a valid species. Neither N. georgiensis, nor N. antarctica Szidat & Graefe, 1967 (syn. Crassicutis antarcticus Szidat & Graefe, 1967), as described by Zdzitowiecki et al. (1993), represent N. antarctica, as originally described, and N. georgiensis and N. antarctica, as described by Zdzitowiecki et al. (1993), may be conspecific.

Keys to the species of Athesmia Loss, 1899 (Digenea: Dicrocoeliidae: Dicrocoeliinae), with the description of a new species from the clapper rail, Rallus longirostris Boddaert (Gruiformes: Rallidae), from Galveston, Texas, U.S.A.

Eleven specimens of a previously undescribed species of Athesmia Looss, 1899 were recovered from six clapper rails, Rallus longirostris Boddaert (Rallidae), collected from November, 1984 through October, 1995 from the Galveston, Texas area of the Gulf of Mexico. Species of Athesmia can be divided into two body types based on the posterior extent of the ceca relative to the vitelline field (vitellarium): the attilae type where the ceca may be uneven, but they both extend at least to near the level of the posterior margin of the vitelline field, or more commonly surpass the vitelline field posteriorly and the heterolechithodes type where the cecum on the side of the vitelline field terminates well above the posterior margin of the vitelline field, usually near its anterior extremity, while the cecum opposite the vitelline field extends at least to the level of the posterior margin of the vitelline field, or more commonly surpasses the vitelline field posteriorly. Athesmia ralli n. sp. is assigned to the attilae type. The new species is most similar to Athesmia butensis Petri, 1942, but differs from this species by having a longer space from posterior testis to ovary (600-790 compared to less than 200), which represent a larger percentage of the total body length (7-8% compared to 2%) and a larger maximum egg size (47 by 29 compared to 42 by 25). The new species further differs from A. butensis by having a somewhat larger body, a longer forebody and the vitelline field reaches posteriorly to the posterior third of the body in the new species but is confined to the middle third of the body in A. butensis. A key to species also is provided.

A new species of Neolebouria Gibson, 1976 (Opecoelidae: Plagioporinae) from the whitecheek monocle bream, Scolopsis vosmeri (Perciformes: Nemipteridae), from the Panjim coast at Goa, with a checklist of parasites previously reported from this fish.

Neolebouria capoori n. sp. (Opecoelidae: Plagioporinae) is described from the whitecheek monocle bream, Scolopsis vosmeri (Bloch) (Perciformes: Nemipteridae) from the Panjim coast on the central west coast of India at Goa. The new species differs from both Neolebouria cantherhini (Li, Qiu & Zhang, 1988) as originally described from Thamnaconus modestus (Günther) (syn. Cantherines modestus Günther ) and Neolebouria confusum (Overstreet, 1969) as originally described from Ocyurus chrysurus (Bloch) by having the cirrus sac surpassing the ventral sucker posteriorly in N. cantherhini and being entirely preacetabular in N. confusum compared to terminating near the midlevel of the ventral sucker in N. capoori n. sp. The new species is most similar to N. confusum, but it further differs from this species by having the vitelline fields terminating near the level of the esophageal bifurcation compared to terminating near the level of the posterior margin of the pharynx, a larger sucker ratio (1:1.7-1:2.0 compared to 1:1.4-1:1.7), a somewhat shorter cirrus sac relative to body length (160-448, representing 9-18% of the body length compared to about 367, representing 22%), and the egg of the new species has a boss at the anopercular end that is not present in N. confusum. This study represents the first report on an opecoelid from S. vosmeri. A review of the parasites reported from S. vosmeri is included.

Towards resolving the problematic status of the digenean genus Astiotrema Looss, 1900: Taxa excluded from Astiotrema (sensu stricto) with special reference to plagiorchioid genera closely related to the restricted concept of Astiotrema.

The restricted concept of Astiotrema Looss, 1900 has been revised to include only eight species and various representative synonyms. However, several remaining taxa of Astiotrema (sensu lato) still need more inspection and scrutiny to determine their correct taxonomic position. Following a comprehensive review, four new genera are erected to accommodate some taxa excluded from Astiotrema (sensu stricto), three of which are closely related to this restricted concept of Astiotrema. Plesioastiotrema n. gen. is erected to accommodate Plesioastiotrema monticellii (Stossich, 1904) n. comb. (syn. Astiotrema monticellii Stossich, 1904) as the type-species and Plesioastiotrema magniovum (Fischthal & Kuntz, 1965) n. comb. (syn. Astiotrema magniovum Fischthal & Kuntz, 1965). Homeoastiotrema n. gen. is established for its type-species, Homeoastiotrema turneri (Bray, Van Oosterhout, Blais & Cable, 2006) n. comb., to accommodate Astiotrema turneri Bray, Van Oosterhout, Blais & Cable, 2006. Ichthyastiotrema n. gen. is erected with its type-species, Ichthyastiotrema fotedari (Dhar, 1977) n. comb. (syn. Astiotrema fotedari Dhar, 1977). A distinct morphologically and taxonomically distant taxon from Astiotrema (sensu stricto) is proposed in its own genus, Alloastiotrema n. gen. with its type-species, Alloastiotrema birmanii (Khan, Gul-E-Lala, Ghazi, Khatoon, Waheed & Khan, 2021) n. comb., to accommodate Astiotrema birmanii Khan, Gul-E-Lala, Ghazi, Khatoon, Waheed & Khan, 2021 and positioned distant from Astiotrema (sensu stricto). Astiotrema erinaceum (Poirier, 1886) Stossich, 1904, Astiotrema trituri Grabda, 1959 and Astiotrema (Biguetrema) tananarivense Deblock & Capron, 1962 are adopted synonyms of Galactosomum erinaceum (Poirier, 1886) Bittner & Sprehn, 1928, Neoastiotrema trituri (Grabda, 1959) Tkach, 2008 and Laiogonimus tananarivensis (Deblock & Capron, 1962) Fischthal & Thomas, 1968, respectively. Astiotrema lazeri El-Naffar, Saoud & Hassan, 1984 and Astiotrema gangeticus Gupta & Singh, 1985 nec Harshey, 1932 are synonymized with Glossidium pedatum Looss, 1899 and Orientocreadium batrachoides Tubangui, 1931, respectively. Based on its contradiction to the diagnosis of members of the Orientocreadiidae Yamaguti, 1958, we declare Orientocreadium lucknowensis Nigam, Chandra, Johri & Saxena, 2015 as incertae sedis. Longigula Qiu, Zhang & Li, 1983 and Kalipharynx Boeger & Thatcher, 1983 are morphologically closest to Astiotrema (sensu stricto) compared to members of the Plagiorchiidae Lühe, 1901 based on both genera possessing a cirrus-pouch with a unipartite, saccular seminal vesicle. The problematic status of Pseudoparamacroderoides Gupta & Agrawal, 1968 (sensu lato), the closest related genus to Astiotrema (sensu stricto), is discussed through evaluating the differential characteristics among listed species to indicate the extent of their validity and identifying the genuine species within this genus to re-evaluate the confusing and overlapping species to help understand their relationships with closely related plagiorchioids. Accordingly, only three species are recognized within Pseudoparamacroderoides Gupta & Agrawal, 1968 (sensu stricto): Pseudoparamacroderoides dongthapensis Truong, Curran & Bullard in Truong, Curran, Dutton & Bullard, 2021; Pseudoparamacroderoides pseudobagri (Wang in Wang, Zhao, Chen & Tao, 1983) n. comb. (syns. Astiotrema pseudobagri [Wang in Wang, Zhao, Chen & Tao, 1983] Karar, Blend, Dronen & Adel, 2021; Gauhatiana pseudobagri Wang in Wang, Zhao, Chen & Tao, 1983); and Pseudoparamacroderoides seenghali Gupta & Agrawal, 1968 (Syn. Pseudoparamacroderoides vittati Kakaji, 1969 n. syn.). Pseudoparamacroderoides raychaudhurii Agarwal & Kumar, 1983 is re-evaluated as Alloglossidium raychaudhurii (Agarwal & Kumar, 1983) n. comb. Anomalomacroderoiditrema n. gen. is erected for the type-species, Anomalomacroderoiditrema keni (Agarwal & Agarwal, 1984) n. comb., to accommodate specimens of Pseudoparamacroderoides keni Agarwal & Agarwal, 1984. Although the morphological convergence of Gauhatiana Gupta, 1953 within the Plagiorchioidea Lühe, 1901 has been suggested, it is neither a plagiorchiid nor a macroderoidid and does not appear closely related to Astiotrema (sensu stricto); it evidently is a member of the Monorchiidae Odhner, 1911. Alloglyptus Byrd, 1950 is taxonomically positioned as a gorgoderoid in the Allocreadiidae Looss, 1902, neither a plagiorchioid taxon nor closely related to Astiotrema (sensu stricto). The ambiguity of the seminal receptacle in some taxa of Astiotrema is discussed.

A NEW SPECIES OF PROSOGONOTREMA (SCLERODISTOMIDAE: PROSOGONOTREMATINAE) FROM THE FLATHEAD GREY MULLET, MUGIL CEPHALUS LINNAEUS (MUGILIFORMES: MUGILIDAE), FROM THE ARABIAN GULF OFF IRAQ.

Prosogonotrema iraqiense n. sp. (Sclerodistomidae: Prosogonotrematinae) is described in the flathead grey mullet, Mugil cephalus Linnaeus (Mugiliformes: Mugilidae), collected from the Arabian Gulf off Iraq during June and October 2019. Currently there are 11 species of ProsogonotremaVigueras, 1940 commonly accepted: Prosogonotrema arabicaYadav, 1980; Prosogonotrema bilabiatumVigueras, 1940 (type species); Prosogonotrema caesionisGu and Shen, 1979; Prosogonotrema diacanthiBilqees and Durrani, 1980; Prosogonotrema karachienseBilqees and Durrani, 1980; Prosogonotrema pavasiLokhande, 1990; Prosogonotrema piscicola (Srivastava, 1949) Gibson, 2002 (Syn. Bhaleraoia piscicolaSrivastava, 1949); Prosogonotrema plataxumGu and Shen, 1979; Prosogonotrema posterouterinaYadav, 1980; and Prosogonotrema symmetricumOshmarin, 1965 originally described from marine fishes, and Prosogonotrema nickoliBilqees and Khan, 1992 described from a freshwater cyprinid. Six additional species that have been considered synonyms of P. bilabiatum are also considered. Prosogonotrema diacanthi is considered a junior synonym of P. piscicola and Prosogonotrema carangiHussain and Rao, 1980nec Velasquez, 1961 is determined to be a species distinct from P. bilabiatum and is reassigned herein as Prosogonotrema aluteri nomen novum per the ICZN. Prosogonotrema iraqiense differs from all currently recognized species in the genus by having the width of the ventral sucker approach or exceed the width of the body and from all except P. pavasi (body length/width ratio 1:1.4-1:1.5) by having a distinctive narrower, more elongate body profile with a larger body length/width ratio (1:5.8-1:6.1 vs. 1: 2.0-1:4.1). A key to the 18 species we recognize in Prosogonotrema is included.

Reconsideration of the species assigned to Faustula Poche, 1926 (Digenea: Microphalloidea) with the proposal of five new genera in the Faustulidae Poche, 1926.

The assignment of species to Faustula Poche, 1926 (Faustulidae Poche, 1926) is reconsidered with the proposal of Gangafaustula n. gen. to accommodate Gangafaustula makundai (Agarwal Verma, 1981) n. comb.; Gobifaustula n. gen. to accommodate Gobifaustula qikouensis (Qui Li, 1995) n. comb.; Lingulitrema n. gen. to accommodate Lingulitrema hilsai (Kumar Agarwal, 1984) n. comb.; Schellitrema n. gen. to accommodate Schellitrema gasterostei (Schell, 1973) n. comb. and Varanasifaustula n. gen. to accommodate Varanasifaustula indica (Agarwal Verma, 1981) n. comb. Faustula hilsai Kumar Agarwal, 1984 is determined to be a species distinct from Faustula hilsai Rizvi, 1971 and F. hilsai Rizvi, 1971 is synonymized with Faustula basiri Hafeezullah Siddiqi, 1970. Faustula rahemii Al-Daraji, 2004 also is synonymized with F. basiri. Faustula pyriformis Kumar Agarwal, 1984 is transferred to Pronoprymna Poche, 1926 as Pronoprymna pyriformis (Kumar Agarwal, 1984) n. comb. Faustula sayori (Yamaguti, 1942) Yamaguti, 1958, now synonymized with Pronoprymna petrowi (Layman, 1930) Bray Gibson, 1980, is renamed Pronoprymna sayori (Yamaguti, 1942) n. comb. based on the presence of an entire (smooth) ovary in P. petrowi (Syn. Monorcheides petrowi Layman, 1930) as originally described, and Faustula varanasiensis (Agarwal Kumar, 1977) is transferred to Bacciger Nicoll, 1914 as Bacciger varanasiensis (Agarwal Kumar, 1977) n. comb. We currently propose the following 5 species be retained in Faustula: F. basiri; Faustula brevichrus (Srivastava, 1935) Yamaguti, 1958; Faustula clupeae (Srivastava, 1935) Yamaguti, 1958; Faustula gangetica (Srivastava, 1935) Yamaguti, 1958 and Faustula keksooni (MacCallum, 1918) Poche, 1926. A revised key to the species of Faustula and a key to the genera within the Faustulidae are provided.

Towards resolving the problematic status of the digenean genus Astiotrema Looss, 1900: An updated concept and revision of species composition for Astiotrema (sensu stricto).

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.

Two New Species of Telorchis (Digenea: Telorchiidae) from a Green Turtle, Chelonia Mydas (Cheloniidae), from the Upper Texas Coast with a Key to North American Species of Telorchis.

Sea turtles are difficult to sample because of their protected status; however, museum collections and sea turtle stranding networks provide unique opportunities for parasitological research. Four gastrointestinal tracts from stranded, endangered green turtles, Chelonia mydas, were collected between 1993 and 1995 from the upper Texas coast and opportunistically sampled for parasite fauna. Two new species of Telorchis, a common freshwater amphibian and reptilian intestinal parasite genus, were found and described. Telorchis marinus n. sp. differs from Telorchis mydas n. sp. by its short body length, lack of pharyngeal glands, long esophagus relative to total body length, short and straight cirrus sac, short ventral sucker to ovary length relative to total body length, and an ovary located in the anterior one-third of body; it differs from its congeners in the number of ovary lengths between the ventral sucker and ovary, the number of ventral sucker lengths the cirrus sac extends beyond the posterior margin of the ventral sucker, and the vitelline field extent. Telorchis mydas differs from its congeners in the number of ovary lengths between the ventral sucker and ovary, the number of ventral sucker lengths the cirrus sac extends beyond the posterior margin of the ventral sucker, and the combination of having its ovary position near the midbody and a long, sinuous cirrus sac that is 35-44% of the total body length. Given the taxonomic complexities within Telorchis, a revised key to North American species is provided using morphological characteristics to assist future researchers in delineating true species and appropriate synonymies with molecular explorations. We reject the majority of synonymies in the genus until molecular data are available; we accept the synonymies of Telorchis necturi as Telorchis stunkardi and Telorchis gutturosi as Telorchis chelopi. Both Telorchis linstowi and Telorchis stossichi should be considered as species inquirenda. This is the first confirmed report of Telorchis from a marine host and the first report on parasites of cheloniid sea turtles in Texas, and this study adds to the ever-growing evidence that collections are essential to understanding biodiversity.

A new genus and species of Anchitrematidae Mehra, 1935 (Digenea: Gorgoderoidea) in a freshwater fish from the River Nile at Qena, Egypt with amendation of the family.

Museum specimens of a previously unknown species of the Anchitrematidae from a freshwater fish collected from the River Nile at Qena, Egypt were examined. This species is somewhat similar to species of Anchitrema, but was found to have a thick, continuous, shelf-like rim around the periphery of the ventral aspect of the distome, the lateral aspect of the forebody was composed of large internal patches of lightly vacuolated, somewhat glandular cells that formed pad-like structures (pelops-like structures), and it possessed a uterine seminal receptacle; characteristics that previously have not been found in any species in the family. Species currently assigned to Anchitrema or Mujibia (the only two genera in the family) are known only from reptiles and mammals and no species has previously been reported from a freshwater fish. We feel that these differences are sufficient enough to warrant the erection of Piscianchitrema n. gen. and amendation of the family. We support the synonymies of Anchitrema congolense with Anchitrema latum, and Anchitrema lucknowensis with Anchitrema indicum. The current status of species previously described in the family is discussed, and keys to the genera and species of Anchitrema are provided.

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.

A new cyclocoelid (Digenea) genus from the grey-winged trumpeter, Psophia crepitans (Aves: Gruiformes: Psophiidae), from Guyana.

Six specimens representing a new genus of cyclocoelid, Psophiatrema greineri n. gen., n. sp. (Digenea: Cyclocoelidae: Cyclocoelinae), were collected from the air sacs of a common or grey-winged trumpeter, Psophia crepitans (Gruiformes: Psophiidae), from Guyana on 19 January 2001. The bird was being maintained in an aviary at Emerald Forest Bird Gardens, Fallbrook, California. The new genus has an intertesticular ovary forming a triangle with the testes, placing it in Cyclocoelinae. There are currently 2 genera recognized in Cyclocoelinae: Cyclocoelum and Selfcoelum. The new genus is most similar to Selfcoelum by having a postpharyngeal genital pore, but differs from both Cyclocoelum and Selfcoelum by having the vitelline fields confluent posteriorly. A revised key to the Cyclocoelinae is provided to include the new genus, and the subfamily diagnosis is emended to reflect that the vitelline fields can be either confluent or not posteriorly.

Re-evaluation of the species composition of Bashkirovitrema Skrjabin, 1944 (Digenea: Echinostomatidae), with the description of two new species of this genus and the proposal of Kostadinovatrema novaeguiniense n. g., n. sp.

A comparison of specimens previously identified as Bashkirovitrema incrassatum (Diesing, 1850) from the African or cape clawless otter Aonyx capensis, and the speckle-throated or spotted-throated otter Hydrictis maculicollis from the Old World with specimens and descriptions of B. incrassatum from the New World showed that those from Africa (Bashkirovitrema africanum n. sp.) had a more extensive distribution of the vitelline fields than either B. canadense n. sp. from the northern river otter Lontra canadensis and the American mink Neovison vison (North America) and B. incrassatum from the Neotropical river otter Lontra longicaudis (South America). B. africanum n. sp. further differs from B. canadense n. sp. by having a smaller body, shorter forebody, smaller oral sucker, longer cirrus, shorter intertesticular space, shorter post-testicular space and longer eggs. B. canadense n. sp. can be distinguished from B. incrassatum by having a longer body, longer forebody, smaller sucker ratio, smaller testes, greater distance between the ventral sucker and the ovary, shorter cirrus-sac, longer post-testicular space and narrower eggs. B. africanum n. sp. differs from B. incrassatum by having a smaller ventral sucker, larger ovary, shorter cirrus-sac, smaller intertesticular space, larger post-testicular space and longer eggs that are not as wide. Kostadinovatrema n. g., as represented by K. novaeguiniense n. sp., can be separated from species of Bashkirovitrema Skrjabin, 1944 by having a wider body width to length profile, a head collar that is narrower than the forebody and armed with 33 rather than 27 collar spines, an ovary that is further removed anteriorly from the testes, and a dorso-ventrally flattened hindbody that is nearly as broad as the forebody. The new genus differs from Hypoderaeum Dietz, 1909 and Moliniella Hübner, 1939 by having 33 head collar spines.

Occurrence of Podocotyle Dujardin, 1845 (Opecoelidae, Podocotylinae) in three species of deep-sea macrourids from the Gulf of Mexico and Caribbean Sea with an updated key to species and host-parasite checklist.

Podocotyle pearsei Manter, 1934 is documented from the intestine of Vaillant's grenadier, Bathygadus melanobranchus Vaillant (Macrouridae: Bathygadinae), collected from the northeastern and western Gulf of Mexico from 783-841 m depth. The finding of P. pearsei in B. melanobranchus represents the first originally published report of this genus from this host and the fifth documented host species for P. pearsei. We report three unidentified species of Podocotyle, represented by one individual each, from the intestine of the western Atlantic grenadier, Nezumia atlantica (Parr) (Macrouridae: Macrourinae), and from Bathygadus favosus Goode Bean (Macrouridae: Bathygadinae) found at 637 m, 710 m and 1,143 m depths in the northeastern Gulf of Mexico off Florida and from the Caribbean Sea off Colombia. We provide a checklist of the parasites known from the three macrourid species relevant to this study, comment on the biogeography of the five species of Podocotyle now known from the deep sea and discuss the low host specificity observed across this genus. The high number of fish hosts for Podocotyle (i.e. type hosts include at least 22 piscine families) encompassing a wide phylogenetic diversity and diet makes it unlikely that members of a single genus could evolve such a broad array of life histories (i.e. utilize dissimilar intermediate hosts), and we predict in the future that Podocotyle will be taxonomically divided up. Morphological and especially molecular work is needed for Podocotyle as well as for other digenean genera known to inhabit the deep sea. Podocotyle sp. 1 2 represent the first originally published reports of this genus from N. atlantica while Podocotyle sp. 3 represents the first report of this genus from B. favosus. Podocotyle koshari Nagaty, 1973 is declared a species inquirenda, and a dichotomous key to the 27 species of Podocotyle we recognize is provided.

New species of Prodistomum Linton, 1910 (Digenea: Lepocreadiidae) from the longtail bass, Hemanthias leptus (Ginsburg, 1952) in the Bay of Campeche, Gulf of Mexico.

Prodistomum lichtenfelsi n. sp. (Digenea: Lepocreadiidae) is described; it was obtained from the intestine of the longtail bass, Hemanthias leptus (Ginsburg), collected from the Bay of Campeche in the Gulf of Mexico. This is the first record of a parasite from this host. Prodistomum lichtenfelsi n. sp. is similar to P. hynnodi, P. menidiae, and P. waltairensis in that it possesses a prepharynx that is distinctly shorter (153 microm [110-210] long) than the combined length of the esophagus (163 microm [110-220] long) and the pseudoesophagus (137 microm [120-170] long), but it differs from them in having an excretory vesicle that extends into the forebody, a smooth ovary and testes, and vitellaria that extend to the posterior level of the esophagus. An updated key to the 12 nominal species within Prodistomum is given, and the diagnosis of the genus is emended to include species possessing a sinuous external seminal vesicle.

Diphyllobothrium stemmacephalum Cobbold, 1858 (Diphyllobothriidea) from common bottlenose dolphin, Tursiops truncatus (Montagu) from the Texas Gulf coast, USA.

Cobbold (1858) established Diphyllobothrium Cobbold, 1858 with the description of Diphyllobothrium stemmacephalum Cobbold, 1858 from the common harbor porpoise, Phocoena phocoena (Linnaeus) (Phocoenidae), from the North Sea off Scotland. Diphyllobothrium stemmacephalum typically has been reported from a number of Phocoenidae and Delphinidae hosts from a variety of localities: common harbor porpoise from the northern Atlantic Ocean, Baltic Sea and Black sea (e.g. Cobbold, 1858; Delyamure 1955; Delyamure 1968; Delyamure 1971; Delyamure et al. 1985; Anderson, 1987); bottlenose dolphin, Tursiops truncatus (Montagu), from the Gulf of Mexico (Ward Collins 1959), the Black sea (Delyamure et al. 1985); common harbor porpoise off Newfoundland (Brattey Stenson 1995), the Black Sea (Krivokhizin Birkun 1994 [see Yera et al. 2008]), off Denmark (Herreras et al. 1997); long-finned pilot whale, Globicephala melas [Traill], North Atlantic off Faroe Island (Balbuena Raga 1993); Atlantic white-sided dolphin, Lagenorhynchus acutus [Gray], off Massachusetts (Olson Caira 1999).

Pseudopecoelus mccauleyi n. sp. and Podocotyle sp. (Digenea: Opecoelidae) from the deep waters off Oregon and British Columbia with an updated key to the species of Pseudopecoelus von Wicklen, 1946 and checklist of parasites from Lycodes cortezianus (Perciformes: Zoarcidae).

Pseudopecoelus mccauleyi n. sp. (Opecoelidae: Opecoelinae) is described from the intestine of the bigfin eelpout, Lycodes cortezianus (Gilbert, 1890) (Perciformes: Zoarcidae), collected at 200-800 m depths in the Northeastern Pacific Ocean off Oregon and Vancouver Island, British Columbia. The new species is distinguished by possessing a unique combination of the following diagnostic characters: vitelline fields that extend to the posterior margin of the ventral sucker; a slender, tubular and sinuous seminal vesicle that extends some distance into the hindbody; an unspecialized, protuberant ventral sucker; a genital pore at pharynx level; lobed to deeply multilobed testes; a lobed ovary; and an egg size of 68-80 µm × 30-46 µm. A single specimen of Podocotyle Dujardin, 1845 (Digenea: Plagioporinae) is also described from the intestine of an individual Coryphaenoides sp. (Gadiformes: Macrouridae) collected at 2,800 m depth off Oregon. A listing of parasites from the bigfin eelpout as well as observations of parasite diversity within relevant hosts are offered, new host and locality records are noted, and a brief discussion of Pseudopecoelus von Wicklen, 1946 in the deep sea is presented taking note of the low level of host specificity recorded (i.e. spp. of Pseudopecoelus are now known to parasitize deep-water fish from at least 20 piscine families). A new dichotomous key to the 39 recognized species of Pseudopecoelus is introduced.