The Lepocreadiidae (Digenea) of pomacentrid fishes (Perciformes) from Heron Island,Queensland, Australia

The following lepocreadiid species are described from pomacentrid fishes from the Southern Great Barrier Reef at Heron Island, Queensland: Lepocreadium adlardi n. sp. from Abudefduf bengalensis; L. clavatum from Acanthochromis polyacanthus and Parma polylepis; Lepocreadium sp. from Amblyglyphidodon curacao; Lepocreadium sp. from Pomacentrus cf. wardi; Preptetos xesuri (new synonyms: P. caballeroi, P. pritchardae Toman, 1989 nec Ahmad, 1984) from Parma polylepis plus the acanthurid Naso annulatus; and P. cannoni from Pomacentrus bankanensis.     

Two species of Prodistomum Linton, 1910 (Digenea: Lepocreadiidae) from marine fishes of Australia

Prodistomum angelae (Kruse, 1981) n. comb. [originally Lepocreadium] is redescribed from the type-host, Scorpis georgiana, from off southwestern Western Australia. P. keyam n. sp. is described from Monodactylus argenteus from off southeastern Queensland. It differs from other members of the genus in its short ejaculatory duct. The genus Prodistomum Linton is discussed and redefined, and an updated key and record list of the nine recognised species are given.     

The Lepocreadiidae (Digenea) of fishes from the north-east Atlantic: a review of the genusLepidapedon Stafford, 1904

The genusLepidapedon is subdivided into several species groups and subgroups of species based on the vitelline distribution and the length of the excretory vesicle. The species in each of the subgroups are listed and keys to the species in most subgroups are given. The following north-eastern Atlantic species are described or redescribed:Lepidapedon rachion fromMelanogrammus aeglefinus, Gadus morhua, Aspitrigla cuculus, Merlangius merlangus andPollachius pollachius; L. cambrensis fromEnchelyopus cimbrius; L. sommervillae n. sp. fromTrachyrincus scabrus, T. murrayi andCoryphaenoides guentheri; L. elongatum fromGadus morhua; L. gaevskayae fromCoryphaenoides (Nematonurus) armatus; L. discoveryi n. sp. fromCoryphaenoides (Nematonurus) armatus; L. arlenae n. sp. fromTrachyrincus scabrus andT. murrayi; L. mariannae n. sp. fromGaidropsarus argentatus; Lepidapedon spp. innom (Elongatum-group) fromCoryphaenoides guentheri andCoryphaenoides (Chalinura) leptolepis; L. desclersae n. sp. fromLepidion eques; L. beveridgei fromCoryphaenoides (Nematonurus) armatus andC. (Chalinura) mediterraneus; andL. zubchenkoi fromCoryphaenoides (Chalinura) leptolepis andC. (C.) profundicolus. The phylogeny, host-specificity and zoogeography of the genus are briefly discussed.     

Description of three species of Holorchis Stossich, 1901 (Digenea: Lepocreadiidae) from marine fishes off Corsica

Three species of Holorchis are redescribed from marine fishes from off Corsica. They are: Holorchis pycnoporus from Diplodus vulgaris, D. sargus, Lithognathus mormyrus, Pagellus erythrinus, Sparus pagrus and Symphodus roissali; H. micracanthum from Sparus pagrus and Pagellus erythrinus; and H. legendrei from Mullus surmuletus. The characteristics differentiating these species are discussed, in particular those separating H. pycnoporus and H. legendrei, species which previously have been considered synonyms. The internal morphology of the cirrus-sac differs distinctly between these forms, which also have microhabitat and host differences.     

The Lepocreadiidae Odhner, 1905 (Digenea) of fishes from the north-east Atlantic: summary paper,with keys and checklists

Results published in seven previous papers on the Lepocreadiidae are summarised and keys are given to the 19 species of lepocreadiid parasite from north-eastern Atlantic fishes. Diagnoses for the family and the two subfamilies represented in the north-eastern Atlantic are presented. Parasite-host and host-parasite lists, arranged in taxonomic order, are given. The NE Atlantic fauna is dominated numerically by members of the subfamily Lepidapedinae, which occur most frequently in gadiform fishes, often in the deep-sea.The three lepocreadiine forms are parasites of cosmopolitan fishes or fish families that predominate in warm waters.     

Lepidapedon spp. (Digenea: Lepocreadiidae) from deep-sea gadiform fishes of the NW Atlantic Ocean,including four new species

Five species are described from fishes in deep waters of the northwestern Atlantic Ocean: Lepidapedon gaevskayae n. sp. from Coryphaenoides (Nematonurus) armatus; L. merretti n. sp. from Phycis chesteri; L. zubchenkoi n. sp. from Coryphaenoides (Chalinura) leptolepis; L. beveridgei n. sp. from C. (N.) armatus; and Lepidapedon sp. innom. from Antimora rostrata. The genus Lepidapedon is discussed and divided into groups of species distinguished by the vitelline distribution and the extent of excretory vesicle. The new species are placed in their appropriate groups and differentiated from the other species in the group.     

Amphicreadium n. g. (Digenea: Lepocreadiidae) from monacanthid fishes (Tetraodontiformes) from the coast of northern Tasmania

A new lepocreadiid genus, Amphicreadium, is erected for the species A. denspeniculus n. sp. from Acanthaluteres vittiger and for an unnamed species from Meuschenia freycineti, both from off northern Tasmania. The new genus is distinguished from all other members of its family by its amphistomatous body plan.     

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.     

Two Lepotrema Ozaki, 1932 species (Digenea: Lepocreadiidae) from marine fishes from the southern Great Barrier Reef, Queensland, Australia

The genus Lepotrema Ozaki, 1932 is revived and redefined. Its main diagnostic characters are the dorsal excretory pore, the muscular development of the distal metraterm and the trilobate ovary. It is considered to contain five species, to which a key is given. Lepotrema clavatum Ozaki, 1932 is briefly redescribed from Amanses scopas and Sufflamen chrysopterus, and L. canthescheni n. sp. is described from Cantheschenia grandisquamis, based on material from the southern Great Barrier Reef. L. canthescheni is distinguished by its vitelline and uterine distribution. The other three recognised species are: L. adlardi (Bray, Cribb & Barker, 1993) n. comb., L. incisum (Hanson, 1955) n. comb. and L. xanthichthydis (Yamaguti, 1970) n. comb., all three having originally been placed in Lepocreadium.     

Multivariate analyses of metrical features in the Lepidapedon elongatum (Lebour, 1908) species-complex (Digenea,Lepocreadiidae) in deep and shallow water gadiform fishes of the NE Atlantic

One hundred and eleven Lepidapedon elongatum-like worms from five gadiform fish species in the North Atlantic are compared using multivariate analyses of 22 metrical features. A principal component analysis followed by a discriminant analysis indicate multivariate morphological differences between worms in the different hosts. It is argued that the forms in the five host species, Gadus morhua, Onogadus argentatus, Trachyrhynchus trachyrhynchus, Coryphaenoides (Nematonurus) armatus and Lepidion eques, should be considered separate oioxenic species.     

Phylogenetic analysis of Alloglossidium (Digenea: Macroderoididae) and related genera: life-cycle evolution and taxonomic revision

A phylogenetic analysis was performed on 13 species of digenetic trematodes in the Macroderoididae, including 10 species of Alloglossidium, 2 species of Alloglossoides, and Hirudicolotrema richardsoni. The evolution of the unusual life-cycle patterns in the group was assessed in light of the proposed phylogeny. The results support previous hypotheses that taxa with a 3-host life cycle involving catfish as definitive hosts are basal to taxa with a 2-host life cycle involving invertebrates such as crustaceans and leeches as definitive hosts. Our results also strongly suggest that species maturing in leeches evolved from an ancestor that matured in crustaceans. Our phylogeny places Alloglossoides and Hirudicolotrema within Alloglossidium, showing Alloglossidium to be paraphyletic. To achieve a natural classification, Alloglossoides and Hirudicolotrema are synonymized with Alloglossidium, and a revised generic diagnosis for Alloglossidium is given.     

Phylogenetic analysis of the suborder plagiorchiata (Platyhelminthes, Digenea) based on partial lsrDNA sequences

The phylogenetic relationships and systematic position of the members of the suborder Plagiorchiata, one of the derived and most diverse groups of Digenea, have always been controversial. Here, we present a phylogeny of this group based on the analysis of partial sequences of the lsrDNA in 28 species representing 13 families of Plagiorchiata, as well as four outgroups. Our results show that the Plagiorchiata, as considered by most authors, is not monophyletic, and that the superfamilies Opecoeloidea, and most probably Dicrocoelioidea and Gorgoderoidea, may have to be removed from this suborder. According to our results, the Plagiorchiata includes only parasites of terrestrial vertebrates. We find the Plagiorchiata to be composed of two well-supported clades which can be ranked as superfamilies: (1) Plagiorchioidea, including the Plagiorchiidae, Haematoloechidae, Telorchiidae, Brachycoeliidae and Leptophallidae; and (2) Microphalloidea containing the Microphallidae, Prosthogonimidae, Lecithodendriidae and Pleurogenidae. The genetic analysis also allowed revision of the position of several taxa of Plagiorchiata, including: (1) a confirmation of the position of the Brachycoeliidae within the Plagiorchiata; (2) a close phylogenetic relationships of Macrodera with Paralepoderma, Leptophallus and Metaleptophallus; (3) the grouping of Opisthioglyphe and Telorchis within a distinct and strongly supported clade; and (4) the placement of Allassogonoporus amphoraeformis within the Pleurogenidae, and not close to Lecithodendriidae. Some systematic changes, corresponding to these results, are proposed.     

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.     

Phylogenetic analysis and taxonomy of the poecilioid fishes (Teleostei: Cyprinodontiformes)

Evidence from morphology is used to infer the phylogeny of the superfamily Poecilioidea using other cyprinodontoid fishes as outgroups. The three equally most parsimonious trees resulting from the phylogenetic analysis support the monophyly of the families Anablepidae and Poeciliidae with respect to each other, but the previous taxonomy within the Poeciliinae is not consistent with the resultant phylogenetic trees. The Poeciliidae is recognized with three subfamilies: the Aplocheilichthyinae containing solely Aplocheilichthys spilauchen , the Procatopodinae containing Fluviphylax (Fluviphylacini) and the African lamp-eyed killifishes (Procatopodini), and the Poeciliinae. The inferred hierarchical relationships of included suprageneric taxa are: ((Oxyzygonectinae, Anablepinae) (Aplocheilichthyinae ((Fluviphylacini, Procatopodini) (Alfarini (Priapellini (Gambusini (Heterandrini (Cnesterodontini (Girardini, Poeciliini))))))))). The tribe Alfarini is resurrected and a new tribe, the Priapellini, is described. Tomeurus gracilis is not the most basal poeciliine, and facultative viviparity in Tomeurus is not a plesiomorphic intermediate condition of viviparity retained from the common ancestor of poeciliines. Facultative viviparity in Tomeurus is the result of an evolutionary loss of obligate viviparity. Tomeurus gracilis is recognized as a member of the tribe Cnesterodontini. Lamprichthys tanganicus and Micropanchax pelagicus are not sister taxa, and the pelagic lacustrine habits of these two species are inferred to have evolved independently. Based on the principles of vicariance biogeography, the origin of the Poecilioidea is inferred to have occurred before the separation of Africa and South America.     

Four species of Lepidapedoides Yamaguti, 1970 (Digenea: Lepocreadiidae) from fishes of the southern Great Barrier Reef, with a tabulation of host-parasite data on the group

Four species of the genus Lepidapedoides Yamaguti, 1970 are described from Heron Island, southern Great Barrier Reef, Queensland, Australia. They are: Lepidapedoides angustus n. sp. in Epinephelus fasciatus (type-host), E. cyanopodus, E. merra, E. quoyanus, E. ongus, Cephalopholis miniata and Diploprion bifasciatum; L. dollfusi (Durio & Manter, 1968) n. comb. [originally Neolepidapedon] in Epinephelus cyanopodus; L. ovale (Yamaguti, 1942) n. comb. [originally Pseudocreadium] in Caesio cuning and Pterocaesio marri; and L. parvulus n. sp. in Pterocaesio marri (type-host) and Caesio cuning. Host and distribution information on the species of the genus are tabulated according to morphological group. Mycterobonacinus Nasir & Gomez, 1977 is considered synonymous with Lepidapedoides, and M. magnifus is considered a synonym of L. nicolli.     

The Australian species of Lobatocreadium Madhavi, 1972, Hypocreadium Ozaki, 1936 and Dermadena Manter, 1945 (Digenea: Lepocreadiidae), parasites of marine tetraodontiform fishes

The genera Lobatocreadium, Pseudocreadium, Hypocreadium and Dermadena are redefined and host lists given. Provisional keys to species of Lobatocreadium, Hypocreadium and Dermadena are presented. The following species are described from (1) the Great Barrier Reef: Lobatocreadium exiguum from Balistapus undulatus and Sufflamen bursa; Hypocreadium cavum n. sp. from Abalistes stellatus (type-host) and Cantheschenia grandisquamis; H. grandisquamis n. sp. from Cantheschenia grandisquamis; Dermadena spatiosa n. sp. from Cantheschenia grandisquamis; and (2) southwestern Australia: D. stirlingi n. sp. from Meuschenia hippocrepis. The following new combinations are made: Lobatocreadium vitellosum (Ozaki, 1936) n. comb. (originally Leptocreadium); Hypocreadium balistes (Nagaty, 1942) n. comb. (originally Pseudocreadium); H. biminensis (Sogandares-Bernal, 1959) n. comb. (originally Pseudocreadium); H. indicum (Madhavi, 1972) n. comb. (originally Pseudocreadium); and H. galapagoensis (Manter, 1945) n. comb. (originally Pseudocreadium). Several nominal species of Pseudocreadium and Hypocreadium are considered incertae sedis.     

Faustulid trematodes (Digenea) from marine fishes of Australia

Twelve species of faustulid trematode are described or redescribed from Australian marine fishes. Bacciger lesteri Bray, 1982 and B. sprenti Bray, 1982 are redescribed from Selenotoca multifasciata from Moreton Bay. It is suggested that the original host record for these species, Mugil sp., was incorrect. The genera Discogastroides, Odontocotyle and Pseudodiscogasteroides are synonymised with Paradiscogaster. The new combinations Paradiscogaster arabi (Hafeezullah & Siddiqi, 1970), P. hainanensis (Shen, 1970), P. indicus (Srivastava, 1939), P. macrostomus (Shimazu & Kamegai, 1990), P. ostracii (Yamaguti, 1934) and P. pritchardae (Gupta & Ahmad, 1978) are proposed. Discogasteroides hawaiensis Hanson, 1955 is synonymised with P. ostracii. P. macrostomus and P. ostracii are redescribed from Ostracion meleagris and O. cubicus from the Great Barrier Reef. P. farooqii Hafeezullah & Siddiqi, 1970 is redescribed from Monodactylus argenteus from Moreton Bay. The following new species are described: P. machidai n. sp. from Pomacanthus semicirculatus and P. sexstriatus from the Great Barrier Reef, P. dweorg n. sp. from Meuschenia galii, P. lobomyzon n. sp. from Tilodon sexfasciatus and P. habilis n. sp. from Pelates octolineatus, all from Western Australia. Antorchis pomacanthi (Hafeezullah & Siddiqi, 1970) Machida, 1975 is redescribed from Pomacanthus semicirculatus and P. sexstriatus from the Great Barrier Reef. The new combination Antorchis intermedius (Madhavi, 1975) is proposed for Parantorchis intermedius. Parayamagutia ostracionis is redescribed from O. cubicus from the Great Barrier Reef. Trigonocryptus conus is redescribed from Arothron hispidus from South-east Queensland and from A. nigropunctatus from the Great Barrier Reef. The new combination Trigonocryptus australiensis (Kurochkin, 1970) is proposed for Pseudodiscogasteroides australiensis. The Echinobrevicecinae is reduced to synonymy with the Faustulidae.     

The Lepocreadiidae (Digenea) of fishes from the north-east Atlantic: review of the genusParalepidapedon Shimazu & Shimura, 1984, with a description ofP. williamsi n. sp.

A new species,Paralepidapedon williamsi, is described from the fishCottunculus microps and an unidentified fish of the suborder Cottoidei in the NE Atlantic Ocean. This species is the first member of the genus to be recognized in the Atlantic Ocean. Its general morphology is similar to that of the other members of the genus, but it is distinguished by its large eggs and the relatively few gland-cells associated with the external seminal vesicle. The genusParalepidapedon, which differs fromNeolepidapedon in the possession of a uroproct, is reviewed and a key to the species given. The genus is considered to include five species.     

Phylogenetic relationships of the stromateoid fishes (Perciformes)

The phylogenetic relationships of all 16 genera (plus Psenes pellucidus) of the suborder Stromateoidei were estimated cladistically based on 43 osteological, myological, and external characters. Thirty equally parsimonious trees were obtained. Based on the strict consensus tree, Centrolophidae was nonmonophyletic, Psenopsis being placed as a sister group of a clade comprising Amarsipus, Ariomma, nomeids, Tetragonurus, and stromateids. Schedophilus formed a sister group relationship with Seriolella. The relationships among the Centrolophus, Hyperoglyphe, Icichthys, Tubbia, Schedophilus+Seriolella clade, and Psenopsis+Amarsipus+Ariomma+nomeids+Tetragonurus+stromateids clade were unresolved. Amarsipus, which is unique within the suborder in lacking a pharyngeal sac, was nested within the stromateoid clade, being a sister group of the clade including Ariomma, nomeids, Tetragonurus, and stromateids. The absence of a pharyngeal sac in Amarsipus was interpreted as a reversal, its presence in the Stromateoidei therefore being considered as a synapomorphy. Ariomma was placed as the sister group of a clade comprising nomeids, Tetragonurus, and stromateids. Monophyly of the Nomeidae and Stromateidae were supported by 2 and 11 synapomorphies, respectively.