Molecular evidence that the genus Cadenatella Dollfus, 1946 (Digenea: Plagiorchiida) belongs in the superfamily Haploporoidea Nicoll, 1914

A re-examination of published lsrDNA sequence data of haploporid digeneans has shown that the genus Cadenatella Dollfus, 1946, hitherto considered a lepocreadioid, is correctly placed within the superfamily Haploporoidea Nicoll, 1914, although its relationships within the superfamily are not resolved. The morphological similarities and differences between Cadenatella and other haploporoids are discussed, and the subfamily Cadenatellinae Gibson & Bray, 1982 is considered the best repository for Cadenatella spp. at present.     

Dramatic phenotypic plasticity within species of Siphomutabilus n. g. (Digenea: Cryptogonimidae) from Indo-Pacific caesionines (Perciformes: Lutjanidae)

A survey of Indo-Pacific lutjanids of the subfamily Caesioninae revealed the presence of Siphodera gurukun Machida, 1910 and two new cryptogonimid taxa from off Heron and Lizard Islands on the Great Barrier Reef, Australia, Ningaloo Reef, Western Australia and Rasdhoo Atoll, Maldives. A combined morphological and genetic characterisation of these species shows that they form a clade distinct from the type-species of Siphodera Linton, 1910, S. vinaledwardsii (Linton, 1901), and warrants the proposal of a new genus. Here we propose Siphomutabilus n. g. and transfer Siphodera gurukun Machida, 1986 as the type-species, Siphomutabilus gurukun (Machida, 1986) n. comb. Siphodera aegyptensis Hassanine & Gibson, 2005 is transferred to Siphomutabilus as S. aegyptensis (Hassanine & Gibson, 2005) n. comb. based on morphological and ecological similarities. Siphomutabilus raritas n. sp. is described from Caesio cuning (Bloch) off Lizard Island and S. bitesticulatus n. sp. is described from Pterocaesio marri Schultz off Heron Island. The two new species are unique in that they have two testes, making their morphology broadly consistent with that of Metadena Linton, 1910, yet the molecular analyses conducted here indicates that they are unequivocally united with Siphomutabilus gurukun (which has multiple testes) to the exclusion of Metadena lutiani (Yamaguti, 1942), which was sequenced here. The dramatic phenotypic plasticity observed among such closely related species of Siphomutabilus suggests a secondary modification of what is generally considered a robust generic diagnostic character within this and other digenean families, highlighting the need for a combined morphological and molecular diagnostic approach when characterising these taxa. Siphodera Linton, 1910 is amended to include just two species, the type-species S. vinaledwardsii (Linton, 1901) Linton, 1910 and S. cirrhiti Yamaguti, 1970, which are distinguished by their lack of oral spines and multiple testes that are primarily extracaecal. Siphodera ghanensis Fischthal & Thomas, 1968 is considered a species incertae sedis here based on significant morphological and ecological differences compared with species of Siphodera and Siphomutabilus n. g.     

Pseudobacciger cheneyae n. sp. (Digenea: Gymnophalloidea) from Weber’s chromis (Chromis weberi Fowler & Bean) (Perciformes: Pomacentridae) at Lizard Island,Great Barrier Reef,Australia

A new species of digenean, Pseudobacciger cheneyae n. sp., is described from the intestines of Weber’s chromis (Chromis weberi Fowler & Bean) from off Lizard Island, Great Barrier Reef, Australia. This species differs from the three described species of Pseudobacciger Nahhas & Cable, 1964 [P. cablei Madhavi, 1975, P. harengulae Yamaguti, 1938 and P. manteri Nahhas & Cable, 1964] in combinations of the size of the suckers and the length of the caeca. The host of the present species is a perciform (Family Pomacentridae) which contrasts with previous records of the genus which are almost exclusively from clupeiform fishes. The genus Pseudobacciger is presently recognised within the family Faustulidae (Poche, 1926) but phylogenetic analyses of 28S and ITS2 rDNA show that the new species bears no relationship to species of four other faustulid genera (Antorchis Linton, 1911, Bacciger Nicoll, 1924, Paradiscogaster Yamaguti, 1934 and Trigonocryptus Martin, 1958) but that instead it is nested within the Gymnophalloidea (Odhner, 1905) as sister to the Tandanicolidae (Johnston, 1927). This result suggests that the Faustulidae is polyphyletic.     

A new species of haploporid (Digenea) from the South China Sea

Megasolena dongzhaiensis n. sp. was collected from the intestine of Scatophagus argus (Linnaeus) (Perciformes: Scatophagidae) from the Dongzhai Bay (110 degrees 32'-37'E, 19 degrees 51'-20 degrees 1'N), Hainan Province, China. It resembles Megasolena acanthuri Machida and Uchida, 1991 in having larger body size, but it differs from the latter species in having an oral sucker that is larger, instead of smaller, than the acetabulum (sucker length ratio 1:0.456-0.494, and width ratio 1:0.61-0.65 in M. dongzhaiensis n. sp., as opposed to 1:1.3-1.7 in M. acanthuri). Moreover, the cuticle is spinose rather than aspinose; there is a band of circular muscle in the pharynx, and its eggs are smaller instead of larger (0.062-0.068 x 0.036-0.039 in M. dongzhaiensis n. sp., compared with 0.087-0.103 x 0.058-0.072 in M. acanthuri). Finally, the intestinal bifurcation is anterior, instead of dorsal, to the acetabulum. It resembles other species of Megasolena Linton, 1910 in having oral sucker larger than the acetabulum, and in having a circular muscle band in the oral sucker and pharynx, but it differs in having a larger body and smaller eggs. This is the first record of a Megasolena species from ray-finned fishes as well as in China.     

Systematics of Crepidostomum species from the Russian Far East and northern Japan,with description of a new species and validation of the genus Stephanophiala

Current article touched upon the issue of the complicated taxonomic status of some species from the genus Crepidostomum collected from the freshwater fish in the rivers of Primorsky region, Sakhalin, and Hokkaido Islands. Primary morphological analyses showed affiliation of the worms to the species C. farionis (Müller, 1784) Lühe, 1909; C. metoecus Braun, 1900b; C. chaenogobii Yamaguti and Matsumura, 1942; C. nemachilus Krotov, 1959. We described the new species Crepidostomum achmerovi sp. nov. that is a sibling species of C. nemachilus. Molecular-genetic investigation have shown that C. nemachilus and C. achmerovi sp. nov. are closely related to C. metoecus in both 28S rDNA and cox1 mtDNA markers. Crepidostomum nemachilus forms a separate branch within the C. metoecus clade on the 28S BI tree with strong statistical support and separate clade in relation to C. metoecus clade on the cox1 BI tree. Values of p-distances between Crepidostomum species were at intergeneric level. Crepidostomum metoecus species complex including five species (C. metoecus, C. nemachilus, C. oschmarini, C. brinkmanni, and C. achmerovi sp. nov.) was reconsidered as independent genus Crepidostomum sensu stricto. Minimum Spanning Network showed that C. nemachilus, C. metoecus and C. achmerovi sp. nov. were separated by large number of mutational events and represent independent phyletic lines. An amended diagnosis is provided for the subfamily Crepidostomatinae, the genera Crepidostomum s. str. and Stephanophiala Nicoll, 1909, along with keys to species of both genera.     

The Lepocreadiidae (Digenea) of fishes of the north-east Atlantic: review of the genera Opechona Looss, 1907 and Prodistomum Linton, 1910

The genera Opechona Looss and Prodistomum Linton are redefined: the latter is re-established, its diagnostic character being the lack of a uroproct. Pharyngora Lebour and Neopechona Stunkard are considered synonyms of Opechona, and Acanthocolpoides Travassos, Freitas & Bührnheim is considered a synonym of Prodistomum. Opechona bacillaris (Molin) and Prodistomum [originally Distomum] polonii (Molin) n. comb. are described from the NE Atlantic Ocean. Separate revisions with keys to Opechona, Prodistomum and ‘Opechona-like’ species incertae sedis are presented. Opechona is considered to contain: O. bacillaris (type-species), O. alaskensis Ward & Fillingham, O. [originally Neopechona] cablei (Stunkard) n. comb., O. chloroscombri Nahhas & Cable, O. occidentalis Montgomery, O. parvasoma Ching sp. inq., O. pharyngodactyla Manter, O. [originally Distomum] pyriforme (Linton) n. comb. and O. sebastodis (Yamaguti). Prodistomum includes: P. gracile Linton (type-species), P. [originally Opechona] girellae (Yamaguti) n. comb., P. [originally Opechona] hynnodi (Yamaguti) n. comb., P. [originally Opechona] menidiae (Manter) n. comb., P. [originally Pharyngora] orientalis (Layman) n. comb., P. polonii and P. [originally Opechona] waltairensis (Madhavi) n. comb. Some species are considered ‘Opechona-like’ species incertae sedis: O. formiae Oshmarin, O. siddiqii Ahmad, 1986 nec 1984, O. mohsini Ahmad, O. magnatestis Gaevskaya & Kovaleva, O. vinodae Ahmad, O. travassosi Ahmad, ‘Lepidapedon’ nelsoni Gupta & Mehrotra and O. siddiqi Ahmad, 1984 nec 1986. The related genera Cephalolepidapedon Yamaguti and Clavogalea Bray and the synonymies of their constituent species are discussed, and further comments are made on related genera and misplaced species. The new combination Clavogalea [originally Stephanostomum] trachinoti (Fischthal & Thomas) is made. The taxonomy, life-history, host-specificity and zoogeography of the genera are briefly discussed.     

Lepocreadiidae Odhner, 1905 and Aephnidiogenidae Yamaguti, 1934 (Digenea: Lepocreadioidea) of fishes from Moreton Bay,Queensland, Australia,with the erection of a new family and genus

Digeneans of the lepocreadioid families Lepocreadiidae Odhner, 1905 and Aephnidiogenidae Yamaguti, 1934 from Moreton Bay, off southern Queensland, Australia, are recorded, along with the erection of a new family, Gibsonivermidae. Molecular data were generated for all representatives of these families collected during this study and a phylogram for members of the superfamily was generated based on the partial 28S rDNA dataset, placing these species in context with those previously sequenced. This phylogenetic analysis demonstrates that the monotypic Gibsonivermis Bray, Cribb & Barker, 1997 is isolated from all other lepocreadioids and supports the erection of Gibsonivermidae n. fam., which is defined morphologically, based particularly on the uniquely elongated male terminal genitalia, the distribution of the uterus in the forebody and the presence of a uroproct. Mobahincia teirae n. g., n. sp. is reported from Platax teira (Forsskål) in Moreton Bay and off Heron Island and New Caledonia. Recognition of this new genus is based on molecular results and the combination of caeca abutting the posterior body wall and the lack of an anterior body scoop or flanges. The following lepocreadioid species are reported from Moreton Bay for the first time: Bianium arabicum Sey, 1996 in Lagocephalus lunaris (Bloch & Schneider), Diploproctodaeum cf. monstrosum Bray, Cribb & Justine, 2010 in Arothron hispidus (Linnaeus), Multitestis magnacetabulum Mamaev, 1970 and Neomultitestis aspidogastriformis Bray & Cribb, 2003 in Platax teira and Opechona austrobacillaris Bray & Cribb, 1998 in Pomatomus saltatrix (Linnaeus). Bianium plicitum (Linton, 1928) is reported from Torquigener squamicauda (Ogilby) for the first time. Sequences of newly collected specimens of Austroholorchis sprenti (Gibson, 1987) indicate that the species forms a clade with other members of the Aephnidiogenidae, agreeing with its morphology. The phylogenetic status of all newly sequenced species is discussed.     

Two species ofCoitocaecum Nicoll, 1915 (Digenea: Opecoelidae) from Moreton Bay,Queensland, Australia

Two species ofCoitocaecum Nicoll, 1915,C. gymnophallum Nicoll, 1915 andC. michaeli n. sp., are recorded, described and figured from the intestine ofAcanthopagrus australis from Moreton Bay, off south east Queensland. The holotype ofC. gymnophallum Nicoll, 1915 is examined, measured and figured for comparison.C. glandulosum Yamaguti, 1934 andC. robustum Wang, 1984 are reduced to synonymy withC. gymnophallum. The host specificity ofCoitocaecum spp. is discussed.     

A new species of Plectognathotrema Layman, 1930 (Trematoda: Zoogonidae) from an Australian monacanthid,with a molecular assessment of the phylogenetic position of the genus

During helminthological examinations of teleost fishes of Ningaloo Reef, Western Australia, a new species of the enigmatic genus Plectognathotrema Layman, 1930 was discovered infecting the pot-bellied leatherjacket Pseudomonacanthus peroni (Hollard). The new species, Plectognathotrema kamegaii n. sp., is formally described, and the status of its four congeners is reviewed. Plectognathotrema hydrolagi Olson, Hanson & Pratt, 1970 is not recognised within the genus, as it differs greatly from its congeners in the form and arrangement of the vitellarium, testes and uterus, and in that it was described from a holocephalan. Plectognathotrema cephalopore Layman, 1930 and P. tsushimaense Kamegai, 1970 are morphologically similar, were described from the same host species and from close geographical localities and are considered synonymous. The new taxon is most similar to P. cephalopore, but differs from it in being much smaller and possessing a distinctly larger oral sucker relative to its body size. The generation of novel partial 28S ribosomal DNA sequences allowed a phylogenetic assessment of the genus and demonstrated that Plectognathotrema clearly belongs in the Zoogonidae Odhner, 1902, rather than in the Fellodistomidae Nicoll, 1909, where it is currently assigned. With the inclusion of Plectognathotrema in the Zoogonidae, there are now three zoogonid genera for which the species are restricted to monacanthid teleosts, i.e. Cephaloporus Yamaguti, 1934, Plectognathotrema and Yamagutiplectognathotrema Parukhin, 1977. Species of these genera share pronounced morphological and ecological affinities and a previously synonymised subfamily, the Cephaloporinae Yamaguti, 1934, is resurrected for them. The host specificity of these trematodes is commented upon.     

Review of haploporid (Trematoda) genera with ornate muscularisation in the region of the oral sucker, including four new species and a new genus

Species of the Haploporidae Nicoll, 1914 with elaborate muscularisation of the oral sucker belong in three trematode genera, including three new species and a new genus from the intestine of fishes in Australian waters. Spiritestis Nagaty, 1948 is resurrected and S. herveyensis n. sp. is described from the mullet Moolgarda seheli (Forsskål) collected in Hervey Bay, Queensland, Australia; the latter differs from S. arabii Nagaty, 1948 in that the position of the genital pore is pharyngeal rather than post-pharyngeal and the geographical range is off Australia rather than the Red Sea. A new genus is proposed for two new species, with a uniquely ornamented oral sucker, which infect Australian scatophagids. Members of Capitimitta n. g. are distinguished from Waretrema Srivastava, 1937, species of which have a simple oral sucker with six radially arranged anterior muscular lobes, in that their oral sucker is V-shaped with six embedded muscular finger-like structures in the anteroventral portion. The relatively small C. darwinensis n. sp., collected from Selenotoca multifasciata (Richardson) at Darwin, Northern Territory, Australia, is distinguished from C. costata n. sp., collected from Scatophagus argus (Linnaeus) in the same locality and S. multifasciata off Brisbane, Australia, and by having smaller eggs, a vitellarium commencing at a level close to the ventral sucker rather than at greater than one ovarian length posterior to the ventral sucker, and shorter tegumental body spines. Sequence data of a c.2,500 bp region of the 3′ end of 18S, the entire ITS region and the 5′ end of the 28S revealed that Spiritestis and Capitimitta are not as closely related as some morphological features would suggest and are probably not the closest relative of each other. What has been reported as Waretrema piscicolum Srivastava, 1937 probably consists of several species, some in different genera, and one, based on material collected by Dr Masaaki Machida, is proposed as Spiritestis machidai n. sp. from Crenimugil crenilabis (Forsskål) off Japan. Phylogenetic hypotheses, based on analysis of an alignment of partial 28S sequences with other haploporids, provide a framework for the evaluation of interrelationships within the Haploporidae. These analyses show that: (1) Spiritestis and Capitimitta are supported within the Haploporidae; (2) branches to Forticulcita Overstreet, 1982, Saccocoelioides Szidat, 1954, Spiritestis and Capitimitta create a clade that is sister to haploporines from the Mediterranean Sea; (3) the branch to Saccocoelioides, Spiritestis and Capitimitta create a polytomy; and (4) the two new species of Capitimitta, plus an immature specimen of an unnamed species, form a monophyletic clade.     

Two new species of <Emphasis Type="Italic">Bacciger</Emphasis> Nicoll, 1914 (Trematoda: Faustulidae) in species of <Emphasis Type="Italic">Herklotsichthys</Emphasis> Whitley (Clupeidae) from Queensland waters

Two new species of Bacciger Nicoll, 1914 (Faustulidae) are described infecting clupeids collected from the waters off Queensland, Australia; Bacciger minor n. sp. is described from Herklotsichthys castelnaui (Ogilby) in Moreton Bay, southern Queensland and Bacciger major n. sp. is described from Herklotsichthys quadrimaculatus (Rüppell) collected off Lizard Island, on the northern Great Barrier Reef. The two species both differ from previously described species of Bacciger in the combination of their generally elongate bodies, an entire rather than deeply lobed ovary, vitelline follicles that reach to at least the intestinal bifurcation, instead of restricted to further posteriorly but principally distributed in the hindbody, and intestinal caeca extending posteriorly well past the ventral sucker. The two new species have non-overlapping size ranges and differ in their sucker ratios, the distribution of the vitelline follicles and in the shape of the cirrus-sac. ITS2 and 28S rDNA sequence data distinguish the two new species unambiguously. Phylogenetic analysis of available 28S data show they are most closely related to Pseudobacciger cheneyae Sun, Bray, Yong, Cutmore & Cribb, 2014, also recorded off Lizard Island. These are the first faustulids reported from species of Herklotsichthys Whitley, but overall members of the Clupeidae undoubtedly harbours the richest faustulid fauna of any fish family. Baccigeroides ovatus (Price, 1934) n. comb. is proposed for Bacciger ovatus (Price, 1934) Bray & Gibson, 1980 (syn. B. opisthonema Nahhas & Cable, 1964) based on the position of the genital pore being far anteriorly removed from the ventral sucker.     

Trematodes of Red Sea fishes: <Emphasis Type="Italic">Hexangium brayi</Emphasis> n. sp. (Angiodictyidae Looss, 1902) and <Emphasis Type="Italic">Siphodera aegyptensis </Emphasis>n. sp. (Cryptogonimidae Ward, 1917), with a review of their genera

Specimens of the marine fishes Siganus luridus (Siganidae) and Caesio suevica (Lutjanidae) were caught in the Red Sea off the coast of Sharm El-Sheikh, South Sinai, Egypt. Twelve (30%) and eight (17%) fish, respectively, were found to harbour intestinal trematodes. S. luridus was parasitised by Hexangium brayi n.␣sp. (Angiodictyidae) and C. suevica by Siphodera aegyptensis n. sp. (Cryptogonimidae). H. brayi n. sp. is differentiated from the other two species of the genus by the vitelline follicles which are confined to the inter-caecal field, its body shape which is distinctly pyriform, the terminations of the intestinal caeca which are distinctly saccular, the eggs which are few in number, and by the excretory vesicle which gives off a lateral arm on each side that divides into two long collecting ducts. S. aegyptensis n. sp. is most similar to S.␣cirrhiti Yamaguti, 1970, but differs in having a definite number of testes (nine), seven arranged in a ring and the other two situated symmetrically or diagonally within this ring, and vitelline follicles extending posteriorly to the level of the anterior lobes of the ovary. Both genera Hexangium Goto & Ozaki, 1929 and Siphodera Linton, 1910 are reviewed in detail and redefined.     

Phylogenetic analysis of the Enenterinae (Digenea, Lepocreadiidae) and discussion of the evolution of the digenean fauna of kyphosid fishes

Species allocated to the digenean genera Enenterum Linton, 1910 ; Jeancadenatia Dollfus, 1946 ; Cadenatella Dollfus, 1946 ; and Koseiria form a clade within the Lepocreadiidae whose sister group is a clade comprising Neoallolepidapedon Yamaguti, 1965, Callogonotrema , Oshmarin, 1965, Allolepidapedon Yamaguti, 1940, and Bulbocirrus Oshmarin, 1965. Phylogenetic analysis of the Enenterinae based on comparative morphology, produced one most parsimonious tree with a consistency index of 0.72. Cadenatella is paraphyletic. Only 15.3% of character changes are evolutionary losses, supporting earlier reports that parasitic platyhelminths have experienced little secondary simplification during their evolutionary history. The Enenterinae appears to have originated in the Pacific Ocean, becoming associated with kyphosid fishes as a result of an ancient host switch. Subsequent evolutionary diversification reflects widespread geographical dispersal, consistent with the natural history of kyphosids.     

A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains,Namibia

Two new thick‐tail scorpions in the genus Parabuthus Pocock, 1890 are described from the gravel plains of the Central Namib Desert, Namibia: Parabuthus glabrimanus sp. nov. ; Parabuthus setiventer sp. nov. The two new species occupy discrete distributional ranges, allopatric with the closely related species Parabuthus gracilis Lamoral, 1979 and Parabuthus nanus Lamoral, 1979. The distributions of the four species are mapped and a key provided for their identification. Revised diagnoses are provided for P. gracilis and P. nanus. The two new species are added to a previously published morphological character matrix for Parabuthus species and their phylogenetic positions determined in a reanalysis of Parabuthus phylogeny. Parabuthus setiventer sp. nov. is found to be the sister species of P. nanus, whereas P. glabrimanus sp. nov. is sister to a monophyletic group comprising P. gracilis, P. nanus, and P. setiventer sp. nov. The discovery of two new scorpion species endemic to the Central Namib gravel plains contributes to a growing body of evidence that this barren and desolate region is a hotspot of arachnid species richness and endemism. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 159 , 673–710.     

The sexual adult of Cercaria praecox Walker, 1971 (Digenea: Fellodistomidae), with the proposal of Oceroma n. g.

A sexual adult trematode that is considered to be conspecific with the distinctive larval trematode Cercaria praecox Walker, 1971 is reported from the kyphosid fish Scorpis lineolata Kner in Moreton Bay, Queensland, Australia. The sexual adult is consistent with the cercarial body of Cercaria praecox in having a single caecum with an asymmetrical appendix, symmetrical testes immediately posterior to the ventral sucker, and the ovary and vitellarium both well posterior to the testes. This combination of characters is distinct within the Fellodistomidae Nicoll, 1909 and requires the proposal of a new genus, Oceroma n. g. Analysis of 28S rDNA sequences demonstrates that this species forms a clade with Coomera Dove & Cribb, 1995 within the Fellodistomidae. The life-cycle of the species is predicted to require two hosts and to involve the direct ingestion of the cercaria.     

A review of the genus Parahemiurus Vaz & Pereira, 1930 (Digenea: Hemiuridae)

The genus Parahemiurus Vaz & Pereira, 1930 (syn.: Daniella Sahai & Srivastava, 1977) is defined, its major morphological characters discussed and a key to species given. The species P. merus (Linton, 1910) (syns: P. parahemiurus Vaz & Pereira, 1930, P. sardiniae Yamaguti, 1934, P. seriolae Yamaguti, 1934, P. platichthyi Lloyd, 1938, P. atherinae Yamaguti, 1938, P. harengulae Yamaguti, 1938, P. noblei King, 1962) and P. anchoviae Pereira & Vaz, 1930 are described. Other species recognized are P. clupeae Yamaguti, 1953, P. [originally Daniella] madrasensis (Sahai & Srivastava, 1977) n. comb. (syns: P. dussumieriai Hafeezullah, 1981, P. indicus Ahmad, 1981), P. ecuadori Manter, 1940, P. engraulisi Gupta & Jahan, 1977 (syns: P. cameroni Gupta & Ahmad, 1977, P. puriensis Ahmad, 1981, P. simhai Gupta & Gupta, 1978, P. tricanthusi Gupta & Puri, 1984) and P. yanamense Hafeezullah, 1980. Forms considered species inquirendae are P. arripidis Lebedev, 1971, P. clupeae of King (1964), P. dogieli Skrjabin & Guschanskaya, 1953, P. pseudosciaenae Shen, 1985 and P. trachichthodi Lebedev, 1968. Host and locality information is given in detail for all species. The complete life-cycle is not known, but metacercariae are reported in chaetognaths and teleosts. The definitive hosts of Parahemiurus spp. most frequently reported belong in the families Clupeidae and Carangidae and the genus is most commonly reported in temperate and subtropical waters.     

Paraphyly of Conodiplostomum Dubois, 1937

Adult trematodes of the genera Conodiplostomum Dubois, 1937 and Neodiplostomum Railliet, 1919 (Trematoda: Diplostomidae) parasitize the intestines of birds of prey, owls and, rarely, passeriform birds. Although the family is taxonomically unsettled, molecular phylogenetics have not been applied to analyze Conodiplostomum and Neodiplostomum and the reference DNA sequences from adult Diplostomidae are scarce and limit studies of their indistinct larval forms. We analyze the Conodiplostomum and Neodiplostomum spp. found during the examination of Czech birds performed from 1962 to 2017, and we provide comparative measurements and host spectra, including prevalence and intensity; we also provide and analyze the sequences of four DNA loci from eight diplostomid species. Molecular phylogenetic analysis suggested that Conodiplostomum spathula (Creplin, 1829), the type species of this genus, is nested in Neodiplostomum. Thus, we suggest the rejection of Conodiplostomum spathula (Creplin, 1829) and the resurrection of Neodiplostomum spathula (Creplin, 1829) La Rue, 1926 and reclassification of all species of Conodiplostomum with the neodiplostomulum type of metacercariae to Neodiplostomum as well. Conodiplostomum canaliculatum (Nicoll, 1914) is reclassified as Neodiplostomum spathulaeforme (Brandes, 1888). The molecular analysis suggested that Conodiplostomum perlatum (Ciurea, 1911), the species with the neascus type of metacercariae, belongs to Crassiphialinae Sudarikov, 1960. We erect the genus Ciureatrema gen. nov. Heneberg & Sitko and reclassify Conodiplostomum perlatum (Ciurea, 1911) as Ciureatrema perlatum (Ciurea, 1911) and establish it as a type species of Ciureatrema gen. nov. Further research should focus on the evolution of the neascus and neodiplostomulum types of metacercariae, as well as the evolution of the genital cone and pseudosuckers in Diplostomidae.     

The anoplocephalid cestode parasites of the spectacled hare-wallaby Lagorchestes conspicillatus Gould, 1842 (Marsupialia: Macropodidae).

Progamotaenia gynandrolinearis sp. nov. is described from the small intestine of Lagorchestes conspicillatus Gould, 1842 from Barrow I., Western Australia. It is distinguished from other species by the small number of testes arranged in a single transverse row. Progamotaenia lagorchestis (Lewis, 1914) is redescribed. The name Progamotaenia thylogale sp. nov. is proposed for a second species described previously under the name P. lagorchestis. Progamotaenia zschokkei (Janicki, 1905), Progamotaenia festiva (Rudolphi, 1819) and Progamotaenia villosa (Lewis, 1914) were also found in L. conspicillatus.     

A new species,new host records and life cycle data for lepocreadiids (Digenea) of pomacentrid fishes from the Great Barrier Reef,Australia

A new species of lepocreadiid, Opechonoides opisthoporus n. sp., is described infecting 12 pomacentrid fish species from the Great Barrier Reef, Australia, with Abudefduf whitleyi Allen & Robertson as the type-host. This taxon differs from the only other known member of the genus, Opechonoides gure Yamaguti, 1940, in the sucker width ratio, cirrus-sac length, position of the testes, position of the pore of Laurer’s canal, and relative post-testicular distance. The new species exhibits stenoxenic host-specificity, infecting pomacentrids from seven genera: Abudefduf Forsskål, Amphiprion Bloch & Schneider, Neoglyphidodon Allen, Neopomacentrus Allen, Plectroglyphidodon Fowler & Ball, Pomacentrus Lacépède and Stegastes Jenyns. Phylogenetic analyses of 28S rDNA sequence data demonstrate that O. opisthoporus n. sp. forms a strongly supported clade with Prodistomum orientale (Layman, 1930) Bray & Gibson, 1990. The life cycle of this new species is partly elucidated on the basis of ITS2 rDNA sequence data; intermediate hosts are shown to be three species of Ctenophora. New host records and molecular data are reported for Lepocreadium oyabitcha Machida, 1984 and Lepotrema amblyglyphidodonis Bray, Cutmore & Cribb, 2018, and new molecular data are provided for Lepotrema acanthochromidis Bray, Cutmore & Cribb, 2018 and Lepotrema adlardi (Bray, Cribb & Barker, 1993) Bray & Cribb, 1996. Novel cox1 mtDNA sequence data showed intraspecific geographical structuring between Heron Island and Lizard Island for L. acanthochromidis but not for L. adlardi or O. opisthoporus n. sp.