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.     

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.     

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.     

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.     

Opecoelidae (Digenea) from western Mediterranean fishes: three rare species

Three little-known opecoelid digeneans from marine fishes off Corsica, France, are redescribed and their relationships discussed. Plagioporus novella Maillard & Lambert, 1978 from Conger conger is transferred to Podocotyle as P. novella (Maillard & Lambert, 1978) n. comb. The new combinations Podocotyle tohei (Yamaguti, 1970) and P. congeri (Yamaguti, 1970) are formed for species originally assigned to Plagioporus. Podocotyle temensis Fischthal & Thomas, 1970 from Epinephelus guaza is redescribed and compared with the other Podocotyle species reported from the Mediterranean. A third species, Pseudopecoeloides chloroscombri (Fischthal & Thomas, 1970) n. comb. (was Podocotyloides), is redescribed from three Trachurus species and a key to the species of this Pseudopecoeloides is given.     

Isthmiophora Lühe, 1909 and Euparyphium Dietz, 1909 (Digenea: Echinostomatidae) re-defined,with comments on their nominal species

The validity of Isthmiophora Lühe, 1909 in relation to Euparyphium Dietz, 1909 is discussed and confirmed. Isthmiophora melis Schrank, 1788) [the type-species] and I. inermis (Fuhrmann, 1904) n. comb. are redescribed, and diagnoses are given for both genera, along with lists of their presently-accepted constituent species which are commented upon where necessary. A similar list of species previously allocated to these genera is also presented with comments on their current status. A key to the species of Isthmiophora is included. New combinations for species previously attributed to Euparyphium are: Isthmiophora inermis (Fuhrmann, 1904) n. comb., I. beaveri (Yamaguti, 1958) n. comb., I. lukjanovi (Chertkova, 1971) n. comb., I. citellicola (Kadenatsii in Skrjabin & Bashkirova, 1956) n. comb., I. hortensis (Asada, 1926) n. comb., Echinostoma pindchi (Khan & Chishti, 1985) n. comb., Echinoparyphium tripathii (Gupta & Gupta, 1982) n. comb., E. hirundonis (Fischthal & Kuntz, 1976) n. comb., and Hypoderaeum longitestis (Verma, 1936) n. comb. Species attributed to Euparyphium which are here considered species inquirendae are: E. lobata Farooq & Yousuf, 1986 sp. inq., E. ochoterenai Cerecero, 1943 sp. inq., E. sobolevi Ryzhikov, 1965 sp. inq., and E. taiwanense Fischthal & Kuntz, 1976 sp. inq.     

Ten new species of Haliotrema (Monogenoidea: Dactylogyridae) from Australian fish and a revision of the genus

Ten new species of Haliotrema from Australian fish are described and figured: H. cteno-chaeti sp. n. from Ctenochaetus strigosus; H. falcanalis sp. n. from Triacanthus falcanalis; H. lineate sp. n. from Acanthurus lineatus; H. chrysotaeniae sp. n. from Lutjanuschrysotaenia; H. cromileptis sp. n. from Cromileptis altivelis; H. epinepheli sp. n. from Epinephelus merra and E. fasciatus; H. holocentri sp. n. from Holocentrus ruber; Haliotrema chrysostomi sp. n. from Lethrinus chrysostomus and Plectorhinchus pictus; H. fleti sp. n. n. from L. fletus and L. chrysostomus; H. scari sp. N. from Scarus fasciatus.
H. dempsteri (Mizelle & Price, 1964) comb. n. from Acanthrus mata, A. dussumieri and A. xanthopterus: H. johnii (Tripathi, 1959) comb. n. from Lutjanus johni and L. fulviflamma: H. parahaliotrema (Mizelle & Price, 1964) comb. n. from Zebrasoma veliferum and A. grammoptilus: and H. obesa (Caballero, Bravo Hollis & Grocott, 1955) comb. n. from Tetraodon hispidus are redescribed and transferred from the genera Parahaliotrema Mizelle & Price, 1964, Ancyrocephalus Creplin, 1839, Parahaliotrema , and Tetrancistrum Goto & Kikuchi, 1917 respectively.
H. brevis (Mizelle & Price, 1964) comb, n. , H. canescens (Mizelle & Price, 1964) comb. n. and H. zanclus (Mizelle & Price, 1964) comb. n. are transferred from Pseudohaliotrema Yamaguti, 1953; H. eilatica (Paperna, 1965) comb. n. , H. teuthis (MacCallum, 1915) comb. n. , H. triacantha (Tripathi, 1959) comb. n. and H. lethrini (Yamaguti, 1937) comb. n. are transferred from Ancyrocephalus Creplin, 1839.
The generic diagnosis is emended to include the above-mentioned species and the taxonomy of the genus is discussed and the formation of six species groups is proposed.     

Description of Pseudorhabdosynochus shenzhenensis n. sp. (Monogenea: Diplectanidae) and redescription of P. serrani Yamaguti, 1953 from Epinephelus coioides off Dapeng Bay, Shenzhen, China

One new species of diplectanid, Pseudorhabdosynochus shenzhenensis n. sp., is reported and described from the marine fish Epinephelus coioides off Nan'ao, Shenzhen, China. It can be differentiated from previously described species of the same genus by features of the haptoral and vaginal hard-parts. A second species, P. serrani Yamaguti, 1953, originally described from Serranus sp. from the western Pacific Ocean off the Celebes (now called Sulawesi), is redescribed based on new material from E. coioides.     

Two new species of Quasithelazia Maplestone, 1932 (Nematoda: Acuariidae) from Malaysia,with an amended diagnosis and review of the genus

Quazithelazia rostrata n. sp. from Ceyx erithaca (L.) (type-host) and Alcedo euryzona Temminck (Coraciiformes, Alcedinidae) and Q. alata n. sp. from Enicurus ruficapillus Temminck (Passeriformes, Muscicapidae) are described from vicinities of Gombak Biological Station, Selangor, Malaysia; both species are parasitic under the koilin lining of the gizzard. Paratypes of Schistogendra pelargopsis Nandi, De & Majumdar, 1985, a parasite of Pelargopsis capensis (L.) (Alcedinidae) from India, are redescribed and the species is recognised as a junior synonym of the type-species of Quasithelazia, Q. tenuis Maplestone, 1932 (new synonymy), a species originally described from Halcyon smyrnensis (L.) (Alcedinidae) in India. An amended diagnosis of the genus Quasithelazia Maplestone, 1932 is proposed. Currently, this genus includes eight species occurring in the Old World, six of them parasitic in kingfishers (Alcedinidae) and two species parasitic in flycatchers (Muscicapidae). These include, inter alia, Q. halcyoni n. comb. for Viktorocara halcyoni Ryzhikov & Khokhlova, 1964 from Halcyon smyrnensis and H. pileata (Boddaert) in Vietnam and the Russian Far East, Q. microcordonis n. comb. for Rusguniella microcordonis Schmidt & Kuntz, 1971 from Halcyon coromanda major (Temminck & Schlegel) in Taiwan and Q. multipapillata n. comb. for Schistogendra multipapillata Zhang, 1993 from Tarsiger cyanurus (Pallas) (Muscicapidae) in China. Comparative morphological data for Quasithelazia spp. are presented. Schistogendra oligopapillata Zhang & An, 2002 from domestic ducks in China is considered a species incertae sedis.     

A taxonomic revision of the Nematotaeniidae Lühe, 1910 (Cestoda: Cyclophyllidea)

A taxonomic revision of the Nematotaeniidae, involving the examination of over 400 specimens, was undertaken. Some new taxonomic characters have been introduced to allow distinction of the various species. The family contains 18 recognized species in four genera. The genusNematotaenia Lühe, 1910 contains four species, namelyN. chantalae Dollfus, 1957,N. dispar (Goeze, 1782) Lühe, 1910,N. hylae Hickman, 1960, andN. tarentolae Lopez-Neyra, 1944.N. kashmirensis Fotedar, 1966,N. dollfusi, Yuen & Fernando, 1974 andN. viride Mokhtar-Maamouri & Chakroun, 1984 are considered junior synonyms ofN. dispar. N. aurangabadensis Chincholikar & Shinde, 1975,N. lopezneyrai Soler, 1945 andN. mabuiae Shinde, 1968 are consideredspecies inquirendae: the latter species probably belongs in the genusOochoristica Lühe, 1898 (Anoplocephalidae: Linstowiinae). The genusCylindrotaenia Jewell, 1916 is shown to possess two testes per segment and not one as originally proposed:Baerietta Hsü, 1935 is consequently synonymized withCylindrotaenia. Cylindrotaenia is divided into five species-groups on the basis of adult morphology. The first group contains two American species, namelyC. americana Jewell, 1916 andC. idahoensis (Waitz & Mehra, 1961) n. comb. The second group contains species from Australia and New Zealand, namelyC. allisonae (Schmidt, 1980), n. comb.,C. criniae (Hickman, 1960) n. comb.,C. decidua (Ainsworth, 1985) n. comb.,C. hickmani (Jones, 1985) n. comb. andC. minor (Hickman, 1960) n. comb. A third species group consists ofC. jaegerskioeldi (Janicki, 1926) n. comb.,C. magna n. sp. andC. philauti Crusz & Sanmugasunderam, 1971 and occurs in Africa, Sri Lanka and Japan. The fourth group, apparently restricted to Japan, contains a single species,C. japonica (Yamaguti, 1938) n. comb. The fifth group containsC. montana (Yamaguti, 1954) n. comb. and occurs in Japan and Tibet.C. quadrijugosa Lawler, 1939 is synonymized withC. americana, andBaerietta claviformis Yamaguti, 1954 is synonymized withC. japonica. C. baeri (Hsü, 1935) n. comb.,C. chilensis (Puga & Franjola, 1983) n. comb.,C. diana (Helfer, 1948) Lehmann, 1960,C. malayi (Yuen & Fernando, 1974) n. comb. andC. roonwali Nama, 1972 arespecies inquirendae. The genusDistoichometra, Dickey 1921 contains a single species, namelyD. bufonis Dickey, 1921.D. kozloffi Douglas, 1958 andBaerietta enteraneides (Helfer, 1948) Yamaguti, 1959 are reduced to synonymy withD. bufonis. Bitegmen n. g. is proposed to accomodate a single species,B. gerrhonoti (Telford, 1965) n. comb., which was previously included in the genusBaerietta. The present distribution of the Nematotaeniidae is largely related to that of their anuran hosts. Nematotaeniids probably arose in Gondwanaland.     

Monogeneans from <Emphasis Type="Italic">Epinephelus chlorostigma</Emphasis> (Val.) (Perciformes: Serranidae) off New Caledonia,with the description of three new species of diplectanids

Gill monogeneans from the brownspotted grouper Epinephelus chlorostigma (Val.) collected in deep water off the coral barrier reef of New Caledonia, South Pacific, comprise seven species. These include the ancyrocephalid Haliotrema sp., the capsalid Allobenedenia cf. epinepheli Yamaguti, 1968, and five diplectanids, namely Pseudorhabdosynochus epinepheli (Yamaguti, 1938), reported in a previous paper, P. cyanopodus Sigura & Justine, 2008 and P. podocyanus Sigura & Justine, 2008, two species originally described from E. cyanopodus Richardson, P. stigmosus n. sp., P. exoticoides n. sp. and Diplectanum femineum n. sp. P. stigmosus is characterised by a sclerotised vagina with a straight primary canal, large ovoid primary chamber and spherical secondary chamber. P. exoticoides is a highly aberrant species, with a thick-walled male quadriloculate organ and a discoid sclerotised vagina with an exceptional structure. Interestingly, P. exoticoides resembles P. exoticus Sigura & Justine, 2008, a species from E. cyanopodus, and P. stigmosus resembles P. cyanopodus and P. podocyanus, also both from E. cyanopodus, suggesting close relationships between the diplectanid faunae of these two fish species. D. femineum belongs to a group of diplectanids, provisionally classified as ‘Diplectanum’ Diesing, 1858, which all share a small funnel-shaped male copulatory organ. In contrast to other members of this group which have no sclerotised vagina, D. femineum has a sclerotised vagina with the same organisation as those of species of Pseudorhabdosynochus Yamaguti, 1958. This suggests that the species of ‘Diplectanum’ from groupers are closer to Pseudorhabdosynochus than suggested by the structure of the male organs.     

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.

     

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.     

Two new genera,shape Provitellus and shape Ovipusillus,and four new species of Monorchiidae (Digenea) from carangid fishes of Queensland,Australia

Two new genera and four new species of monorchiid digeneans are described from the Great Barrier Reef and Moreton Bay, Queensland. Provitellus turrum n. g., n. sp. from Pseudocaranx dentex and Trachinotus coppingeri is characterised by the presence of vitelline follicles in the forebody, a single testis, a unipartite terminal organ and filamented eggs. Ovipusillus mayu n. g., n. sp. from Gnathanodon speciosus is characterised by the presence of two testes, vitelline follicles overlapping the ventral sucker and a large, complex cirrus-sac that contains a coiled eversible ejaculatory duct joined by the pars prostatica halfway along its length. Paramonorcheides pseudocaranxi n. sp. from Pseudocaranx dentex differs from other species described in this genus in the longer flatter forebody, entire ovary and the well-developed cirrus-sac. Chrisomon gaigai n. sp. from Trachinotus coppingeri and T. botla is characterised by the unflattened forebody and transversely oval pharynx. Chrisomon is redefined to include species of Lasiotocus with a vitellarium composed of clusters of tubular acini, creating the following new combinations: C. albulae n. comb. for L. albulae Overstreet, 1969, C. ulua n. comb. for L. ulua Yamaguti, 1970 and C. weke n. comb. for L. weke Yamaguti, 1970. The diagnosis of Lasiotocus is amended accordingly and the new combinations, L. polynemi n. comb. and L. sunderbanensis n. comb., are created for C. polynemi Dutta, Hafeezullah & Manna, 1994 and C. sunderbanensis Dutta, Hafeezullah & Manna, 1994, respectively. Extrapolation of our collection data suggests that there may be as many as 80 species of monorchiids infecting carangid fishes in Australia and 180 species infecting carangids in all oceans of the world. The latter figure greatly exceeds the number of monorchiids described from all host families to     

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.     

Proposal of a new genus,Doorochen (Digenea: Lepocreadioidea), for reef-inhabiting members of the genus Postlepidapedon Zdzitowiecki, 1993

A new genus, Doorochen n. gen., is erected for four species of Postlepidapedon Zdzitowiecki, 1993, all of which inhabit members of the labroid genus Choerodon Bleeker, the tuskfishes, and which molecular phylogenies have indicated are not congeneric with the type-species, P. opisthobifurcatum (Zdzitowiecki, 1990) Zdzitowiecki, 1993. Doorochen secundum (Durio & Manter, 1968) n. comb. from Choerodon graphicus (De Vis), the Graphic tuskfish, from the Great Barrier Reef (GBR) and New Caledonia is designated the type-species of the new genus. Other species recognised are Doorochen spissum (Bray, Cribb & Barker, 1997) n. comb. from C. venustus (De Vis), the Venus tuskfish, C. cyanodus (Richardson), the Blue tuskfish, and C. graphicus from the GBR; D. uberis (Bray, Cribb & Barker, 1997) n. comb. from C. schoenleinii (Valenciennes), the Blackspot tuskfish, and C. venustus from the GBR and Moreton Bay; and D. philippinense (Machida, 2004) n. comb. from C. anchorago (Bloch), the Orange-dotted tuskfish, from Philippine waters. In addition to these four species, two new species are described: D. zdzitowieckii n. sp. from C. fasciatus (Günther), the Harlequin tuskfish, and C. graphicus from the GBR; and D. goorchana n. sp. from C. anchorago from the GBR and Palau. The genus Postlepidapedon is now considered to comprise just two species, P. opisthobifurcatum and P. quintum Bray & Cribb, 2001. The relationships of Doorochen, Postlepidapedon, Myzoxenus Manter, 1934 and Intusatrium Durio & Manter, 1968 in the family Lepidapedidae Yamaguti, 1958 are discussed.     

A new and a rare parasitic copepod from fishes of Kuwait

Summary A new lernaeopodid copepod, Sparidicola papilliferens n.g., n. sp., is described from Acanthopagrus latus (Pisces: Teleostei) taken in Kuwait. This species is designated as a type of its genus, to which is transferred a second species, originally described as Brachiella lithognathae Kensley & Grindley, 1973, renamed Sparidicola lithognathae (Kensley & Grindley 1973) n. comb. A new name, Neobrachiella pillaii nom. nov., is proposed for Brachiella indica Pillai, 1968. The original name is preoccupied by Brachiella indica Tripathi, 1962, which is also transferred to the genus Neobrachiella Kabata, 1979, as N. indica (Tripathi, 1962) n. comb.     

First report of Litomosa spp. (Nematoda: Filarioidea) from Malagasy bats; review of the genus and relationships between species

The presence of the filarial genus Litomosa in Malagasy bats is demonstrated by the finding of L. goodmani n. sp. from Miniopterus gleni and Litomosa sp. (male unknown) from M. manavi, both in the Special Reserve of Ankarana. These materials are compared to the 22 Litomosa species, including two Indian species originally placed in the genus Litomosoides, L. fotedari (Gupta and Trivedi, 1989) n. comb. and L. tewarii (Gupta and Trivedi, 1989) n. comb., and the new taxon L. seurati n. sp. (= L. beaucournui Bain, 1966 pro parte), type-host Rhinolophus ferrum-equinum, Algeria, distinguished by the narrow area rugosa and the female caudal extremity with two conspicuous points, instead of several small ones. The Malagasy material belongs to a group of species close to the type, L. filaria, which have a male area rugosa composed of cuticular bosses and microfilariae folded within the sheath, and which are parasitic in Vespertilionidae, Hipposideridae and Rhinolophidae from Africa and Europe. The two Malagasy species resemble L. seurati n. sp., L. beshkovi Jancev, 1971, L. chiropterum Ortlepp, 1932, L. adami Petit, 1980 and L. ottavianii Lagrange et Bettini, 1948, with the enlarged third segment of the buccal capsule. L. goodmani n. sp. is distinct with its small size and female caudal extremity with a single point, which is suppressed in old mature worms; the females of Litomosa sp. have two conical points. Relationships among Litomosa species appear to be dependent upon both the chiropteran host groups and the geographical region.     

A redescription of Pseudorhabdosynochus epinepheli (Yamaguti, 1938), the type-species of Pseudorhabdosynochus Yamaguti, 1958 (Monogenea: Diplectanidae), and the description of P. satyui n. sp. from Epinephelus akaara off Japan

Pseudorhabdosynochus epinepheli (Yamaguti, 1938) has been recorded from a variety of hosts, mainly groupers. All type-specimens of Diplectanum epinepheli Yamaguti, 1938, Pseudorhabdosynochus epinepheli Yamaguti, 1958 and Cycloplectanum hongkongensis Beverley-Burton & Suriano, 1981 are figured: it is concluded, as did Kritsky & Beverley-Burton (1986), that the three species are synonymous. In addition, numerous monogenean specimens from a deep-sea grouper, Epinephelus chlorostigma, collected off New Caledonia, South Pacific, were prepared using various methods and described. These specimens are also conspecific with P. epinepheli (Yamaguti, 1938) and represent a new geographical record. This species has a sclerotised vagina with a very characteristic primary chamber. The simultaneous presence of P. lantauensis (Beverley-Burton & Suriano, 1981) and P. epinepheli was noted in both type-slides of D. epinepheli from Japan (host: E. akaara) and C. hongkongensis from Hong Kong (host: E. bruneus). Several causes are suspected for the alleged ‘generalist’ character of P. epinepheli, including the misidentification of either fish or monogeneans and the accidental exchanges of monogeneans between fishes of different species kept alive in the same tank. Finally, the confirmed list of hosts of P. epinepheli includes E. akaara, E. awoara and E. chlorostigma; it is suggested that the latter, a widespread deep-sea fish, serves as a reservoir for the infection of the other species, which are associated with shallow waters. P. satyui n. sp. is described from two specimens found on slides from E. akaara (from the Inland Sea of Japan) deposited by Yamaguti; the new species has a sclerotised vagina with characteristic spherical chambers.

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Résumé   Pseudorhabdosynochus epinepheli (Yamaguti, 1938) a été mentionné chez différents h?tes, surtout des mérous. Tous les spécimens-types de Diplectanum epinepheli Yamaguti, 1938, Pseudorhabdosynochus epinepheli Yamaguti, 1958 et Cycloplectanum hongkongensis Beverley-Burton & Suriano, 1981 sont figurés, et on conclut, comme Kritsky & Beverley-Burton (1986), que les trois espèces sont synonymes. De plus, de nombreux spécimens de monogènes collectés chez un mérou de profondeur, Epinephelus chlorostigma, de Nouvelle-Calédonie, Pacifique Sud, ont été préparés avec des méthodes variées. Ces spécimens sont aussi conspécifiques de P. epinepheli (Yamaguti, 1938) et la Nouvelle-Calédonie représente une nouvelle mention géographique. L’espèce a une vagin sclérifié avec une chambre primaire très caractéristique. La présence simultanée de P. lantauensis (Beverley-Burton & Suriano, 1981) et P. epinepheli a été notée dans les lames-types de D. epinepheli du Japon (h?te, E. akaara) et de C. hongkongensis de Hong-Kong (h?te, E. bruneus). Plusieurs causes sont soup?onnées pour le caractère prétendument ‘généraliste’ de P. epinepheli, dont les mauvaises identifications de poissons, des monogènes, et l’échange accidentel de monogènes chez des poissons gardés vivants ensemble dans un même contenant. Finalement, la liste des h?tes confirmés de P. epinepheli comprend E. akaara, E. awoara et E. chlorostigma. On fait l’hypothèse que E. chlorostigma, espèce de profondeur, a servi de réservoir pour l’infestation des autres espèces, plus associées aux eaux peu profondes. P. satyui n. sp. est décrit de deux spécimens trouvés dans des lames de parasites de E. akaara (de la mer intérieure du Japon) déposées par Yamaguti. La nouvelle espèce a un vagin sclérifié avec des chambres sphériques caractéristiques.

     

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.