Descriptions of Wardula bartolii n. sp. (Digenea: Mesometridae) and three newly recorded accidental parasites of Boops boops L. (Sparidae) in the NE Atlantic

Four species of digeneans parasitic in the bogue Boops boops from the Spanish coast of the NE Atlantic are described. All are new records for this host, but one species is new and the other three are considered to be accidental parasites. Wardula bartolii n. sp. (Mesometridae) is distinguished from its two congeners on the basis of a range of morphometrical features, such as the post-ovarian extent of the uterus, the relative length of the attachment organ, the position of the pharynx and vitelline fields, and the absence of anterior caecal diverticula. The other three species are Lecithaster confusus Odhner, 1905, Aponurus laguncula Looss, 1907 (Lecithasteridae) and Accacladium serpentulum Odhner, 1928) (Accacoeliidae).     

Descriptions of Wardula bartolii n. sp. (Digenea: Mesometridae) and three newly recorded accidental parasites of Boops boops L. (Sparidae) in the NE Atlantic

Four species of digeneans parasitic in the bogue Boops boops from the Spanish coast of the NE Atlantic are described. All are new records for this host, but one species is new and the other three are considered to be accidental parasites. Wardula bartolii n. sp. (Mesometridae) is distinguished from its two congeners on the basis of a range of morphometrical features, such as the post-ovarian extent of the uterus, the relative length of the attachment organ, the position of the pharynx and vitelline fields, and the absence of anterior caecal diverticula. The other three species are Lecithaster confusus Odhner, 1905, Aponurus laguncula Looss, 1907 (Lecithasteridae) and Accacladium serpentulum Odhner, 1928) (Accacoeliidae).     

Merlucciotrema praeclarum (Manter, 1934) (Digenea: Hemiuridae) redescribed from myctophiform and gadiform fishes of the North Atlantic

Merlucciotrema praeclarum (Manter, 1934) is redescribed from the deep-sea benthic fishes Bathysaurus mollis, B. ferox and Cataetyx laticeps from various localities in the northern Atlantic Ocean. The genus is close to Plerurus Looss, 1907, but is retained on the basis of the presence of a muscular sinus-organ and, possibly, a rudimentary or degenerate sinus-sac. The subfamily Plerurinae Gibson & Bray, 1979 and the genus Merlucciotrema are redefined.     

Pygidiopsis ardeae n. sp. (Digenea: Heterophyidae: Pygidiopsinae) in the grey heron Ardea cinerea L. from Denmark

A new species, Pygidiopsis ardeae (Heterophyidae, Pygidiopsinae), is described, using both light and stereoscan electron microscopy, from the grey heron Ardea cinerea L. (Ardeidae) from Denmark. The species has previously (as P. genata) been recorded in dogs fed on plaice and flounders from Danish waters. It developed experimentally in domestic chickens and pigeons. No species of Pygidiopsis Looss, 1907 has previously been described from birds in northern Europe. P. ardeae is very similar to the type-species, P. genata Looss, 1907, from Egypt, but the two species have different life-cycles. P. ardeae differs from P. piclaumoreli Dollfus & Capron, 1958 from Senegal in its size and the disposition of vitelline follicles. P. plana (Linton, 1928) Price, 1933, from a green heron from the eastern USA, is larger than P. ardeae and has a wide, sac-like prepharynx.     

Redescriptions of Aphanurus stossichii (Monticelli, 1891) and A. virgula Looss, 1907 (Digenea: Hemiuridae)

Aphanurus stossichii (Monticelli, 1891) is redescribed from Boops boops (L.) from various localities in the NE Atlantic region (off Spain), the Mediterranean (off Spain and Turkey) and the Black Sea (off Bulgaria). The material from the Atlantic coast of Spain showed differences in egg-size and shape and a characteristic ornamentation of the anterior third of the hermaphroditic duct. A comparison with samples from B. boops collected off Antalya (Turkey) and off the Bulgarian Black Sea coast revealed a considerable size variation and confirmed the presence of tubercles in the terminal part of the hermaphroditic duct. A. virgula Looss, 1907, previously considered a synonym of A. stossichii, is redescribed on the basis of voucher material from Engraulis encrasicolus ponticus Alexandrov collected off the Bulgarian Black Sea coast and previously identified as A. stossichii. A. virgula can be distinguished from A. stossichii by its smaller size and substantially lower range limits for all metrical features, the more posterior position of the base of sinus-sac, and the eggs being less numerous and larger in relation to the size of the body and gonads.     

The morphology and taxonomy of the Antarctic species of Tritonia Cuvier, 1797 (Nudibranchia: Dendronotoidea)

The external morphology and anatomy of the Antarctic nudibranchs Tritonia vorax Odhner, 1926, and Tritonia antarctica Pfeffer in Martens & Pfeffer, 1886, is redescribed in detail and compared with other nominal tritoniids from the Antarctic and Subantarctic waters. Tritonia appendiculata Eliot, 1905, T. challengeriana Eliot, 1907a, non Bergh, 1884, T. chalkngeriana Odhner 1926, non Bergh, 1884, and Marionia cmullata Vicente & Arnaud 1974, non (Couthouy, in Gould 1852), are shown to be synonymous with T. antarctica. Only Tritonia antarctica is a true High Antarctic species, with a distribution around the continental shelf, Antarctic Peninsula and South Georgia. T. vorax is confined to South Georgia and Subantarctic waters.     

Revision of the Antarctic genus Notaeolidia (Gastropoda, Nudibranchia), with a description of a new species

New material from the Atlantic sector of the Antarctic Ocean allows a revision of the Antarctic genus Notaeolidia Eliot, 1905. One new species (Notaeolidia schmekelae sp.n.) is described. N. depressa Eliot, 1905 and N. gigas Eliot, 1905, which arc poorly known, arc redescribed. N. rufopicta Thiele, 1912, N. robsoni Odhner, 1934, N. subgigas Odhner, 1944, N. alutacea Minichev, 1972 and N. flava Minichev, 1972 are synonymized with N. depressa. N. purpurea Eliot, 1905 is synonymized with N. gigas. The monogeneric family Notaeolidiidae Odhner, 1926. is characterized by the following autapomorphy: "nephroproct in front of the genital apertures". Too little is known to elaborate the phylogenetic position of the family Notaeolidiidae within the cladobranch Nudibranchia.     

Redescriptions of two frequently recorded but poorly known hemiurid digeneans, Lecithochirium musculus (Looss, 1907) (Lecithochiriinae) and Ectenurus lepidus Looss, 1907 (Dinurinae), based on material from the western Mediterranean

Two frequently reported but poorly known hemiurid digeneans, Lecithochirium musculus (Looss, 1907) (Lecithochiriinae), from the stomach of Trachinus draco and Citharus linguatula, and Ectenurus lepidus Looss, 1907 (Dinurinae), from the stomach of Spicara maena, are redescribed based on material from off the Barcelona coast of the western Mediterranean. The two species are commented upon, and Lecithochirium israelense Fischthal, 1980 is considered a synonym of L. musculus. Records of the two species in the Mediterranean Basin and North East Atlantic region are summarised.     

A new cryptic species of <Emphasis Type="Italic">Aponurus</Emphasis> Looss, 1907 (Digenea: Lecithasteridae) from Mediterranean goatfish (Teleostei: Mullidae)

The status of the trematode Aponurus laguncula Looss, 1907 in the western Mediterranean is re-assessed by means of a comparative morphological study and rDNA sequences based on newly collected material. A. laguncula (sensu stricto) is redescribed from Trachinus draco L. and a new cryptic species of the ‘A. laguncula complex’, Aponurus mulli n. sp., is described on the basis of abundant material from Mullus barbatus L. (type-host) and M. surmuletus L. off the Spanish Mediterranean coasts. The new species is differentiated from A. laguncula (sensu stricto) by its: significantly larger, elongate body, with maximum width at the level of the ventral sucker; shorter forebody; distinctly larger sinus-sac, seminal receptacle and seminal vesicle, with the latter also being more elongate; vesicular pars prostatica; more anteriorly located vitellarium, which consists of eight globular follicles; and distinctly smaller eggs, which are also smaller in relation to body size and have both their opercular and anopercular poles rounded. The variability and the allometric growth of the morphological characters in the new species were studied in detail, resulting in additional distinguishing features. Sequences of the large subunit rRNA (28S) gene (domains D1–D3) and ITS2 rRNA gene region for the new species have been submitted to GenBank in order to enhance future studies on species differentiation within the ‘A. laguncula complex’.     

A new monorchiid trematode, <Emphasis Type="Italic">Paramonorcheides selaris</Emphasis> n. sp., from the carangid fish <Emphasis Type="Italic">Selar crumenophthalmus</Emphasis> in the Bay of Bengal off the Visakhapatnam coast of India

Paramonorcheides selaris n. sp. is described from the intestine of the carangid fish Selar crumenophthalmus (Bloch) off the Visakhapatnam coast, Bay of Bengal. It is closest to the Australian species P. pseudocaranxi Dove & Cribb, 1998, but differs in its shorter cirrus-sac extending only to the level of the ovary rather than to the level of the testes, in lacking eye-spot pigment and in details of the armature of the terminal genitalia. P. pseudocaranxi of Machida (2005) is regarded as identical to the new species. The validity of Allobacciger Hafeezullah & Siddiqi, 1970, as distinct from Monorcheides Odhner, 1905, is discussed. A key to the six species of Paramonorcheides Yamaguti, 1938 is presented.     

<Emphasis Type="Italic">Dicrogaster perpusilla</Emphasis> Looss, 1902 <Emphasis Type="Italic">sensu</Emphasis> Sarabeev &; Balbuena (Digenea: Haploporidae): a note of caution

Sarabeev & Balbuena (2003) considered Dicrogaster perpusilla Looss, 1902 and D. contracta Looss, 1902 (Digenea: Haploporidae) synonymous. They designated a neotype for the type-species, D. perpusilla, from a sample of specimens ex Chelon labrosus off West Thurrock, UK. The morphology of the material (three specimen lots) studied by these authors was re-examined in detail and compared with their data. The material labelled ‘D. perpusilla’ from off West Thurrock, from which the neotype specimen was selected, consists of 14 specimens; of these one might belong to Haploporus Looss, 1902 and one to Haplosplanchnus Looss 1902. A well-developed genital atrium was observed in 11 of the 12 remaining specimens, and they all possess large saccular caeca and a vitellarium consisting of two groups of loosely coalesced follicles rather than two compact masses. These features suggest that the 12 specimens of this lot may belong to Saccocoelium Looss, 1902, but the state of the material does not permit its reliable identification. The specimen designated by Sarabeev & Balbuena (2003) as the neotype of D. perpusilla represents a neogravid dorso-laterally mounted specimen and is unrecognisable. Although five of the six voucher specimens of these authors may represent Dicrogaster spp., the poor state of this material does not allow its accurate identification. The metrical data obtained from this voucher material indicate that juvenile and laterally mounted specimens have been used in the comparisons upon which the synonymy of D. perpusilla and D. contracta was suggested. The overall conclusion of the study is that the synonymy of D. contracta and D. perpusilla proposed by Sarabeev & Balbuena (2003) is based on questionable material. Since the neotype of D. perpusilla is unrecognisable, and a number of qualifying conditions of the ICZN in its designation were not met, the usage of the original conception of the type-species of Dicrogaster given by Looss (1902) is recommended.     

Prosorhynchine trematodes (Digenea: Bucephalidae) from epinephelines (Perciformes: Serranidae) on the Great Barrier Reef,Australia

Six new species of bucephalid trematodes from the prosorhynchine bucephalid genera Prosorhynchus Odhner, 1905 and Neidhartia Nagaty, 1937 are reported from the epinepheline genera Cephalopholis, Cromileptes, Epinephelus and Variola on the Great Barrier Reef, Australia. Two species of Prosorhynchus and one of Neidhartia are reported from Epinephelus spp., P. jexi n. sp. from E. quoyanus, P. lafii n. sp. from E. fuscoguttatus and N. epinepheli n. sp. from E. maculatus. The other three new species are P. robertsthomsoni n. sp. from Cephalopholis argus, C. cyanostigma and C. miniata, P. conorjonesi n. sp. from Cromileptes altivelis, and P. milleri n. sp. from Variola louti. Extensive examinations of other piscivorous fish species from the Great Barrier Reef have not revealed these six bucephalid species, which appear to be restricted at least to the host genera from which they are reported here.     

Notocotylidae (Digenea) from the Australian water rat Hydromys chrysogaster Geoffroy, 1804 (Muridae)

Notocotylus johnstoni n. sp., N. imbricatus (Looss, 1893) Szidat, 1935 and Catatropis nicolli n. sp. are described from the large intestine and caecum of the Australian water rat Hydromys chrysogaster (Rodentia: Muridae). The water rat is the only known mammalian host of notocotylids in Australia. N. imbricatus, recorded from Tasmania, is a cosmopolitan species which elsewhere uses birds and bithyniid snails as definitive and intermediate hosts respectively. In Tasmania bithyniid snails are unknown and the only known definitive host is a mammal. In view of this it is possible that the material examined represents a species distinct from N. imbricatus. Catatropis gallinulae Johnston, 1928 is found to have three rows of ventral papillae and thus to belong to the genus Notocotylus. The new combination Notocotylus gallinulae (Johnston, 1928) is a senior homonym of Notocotylus gallinulae El-Naffar & Khalifa, 1983 which is replaced with Notocotylus elnaffari nom. nov.     

A revision of the Haploporinae Nicoll, 1914 (Digenea: Haploporidae) from mullets (Mugilidae): <Emphasis Type="Italic">Haploporus</Emphasis> Looss, 1902 and <Emphasis Type="Italic">Lecithobotrys</Emphasis> Looss, 1902

The status of the nominal species of Haploporus Looss, 1902 and Lecithobotrys Looss, 1902 is re-assessed by means of a comparative morphological study based on newly collected specimens from the western Mediterranean, the re-examination of museum material and a critical evaluation of published data. H. benedeni (Stossich, 1887) (type-species) is described and H. lateralis Looss, 1902 is considered to be its junior synonym. Additional data are given for H. pseudoindicus Rekharani & Madhavi, 1985, H. spinosus Machida, 1996 and H. magnisaccus Machida, 1996. Species parasitising Valamugil spp. from the Indo-West Pacific region, H. indicus Rekharani & Madhavi, 1985, H. spinosus, H. magnisaccus, H. mugilis Liu & Yang, 2002 and H. muscolosaccus Machida, 2003, are considered incertae sedis with respect to their generic affiliation. H. pacificus (Manter, 1963) (syn. Neohaploporus pacificus Manter, 1963), H. pseudoindicus and H. musculosaccus are designated as species inquirendae and H. lossii Al-Bassel, 1990 is considered to be a nomen nudum. Lecithobotrys putrescens Looss, 1902 is described based on newly collected material from Liza spp. Pseudolecithobotrys n. g. is erected to accommodate Lecithobotrys stomachicola Machida, 1996, as P. stomachicola (Machida, 1996) n. comb., from the North Pacific. L. aegyptiacus Hassan, El-Aziz, Khidr & Abu Samak, 1990 is considered to be a synonym of Saccocoelium tensum Looss, 1902, and L. brisbanensis (Martin, 1974) (syn. Paralecithobotrys brisbanensis Martin, 1974), L. vitellosus Sharma & Gupta, 1970 and L. suezcanali Nisreen Ezz El-Dien, Abdel-Rahman, El-Gawady, Imam & Fahmy, 1990 are regarded as species inquirendae. New generic diagnoses are presented for both Haploporus and Lecithobotrys.

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Molecular phylogenetic analysis of the Microphalloidea Ward, 1901 (Trematoda: Digenea)

Phylogenetic interrelationships of 32 species belonging to 18 genera and four families of the superfamily Microphalloidea were studied using partial sequences of nuclear lsrDNA analysed by Bayesian inference and maximum parsimony. The resulting trees were well resolved at most nodes and demonstrated that the Microphalloidea, as represented by the present data-set, consists of three main clades corresponding to the families Lecithodendriidae, Microphallidae and Pleurogenidae + Prosthogonimidae. Interrelationships of taxa within each clade are considered; as a result of analysis of molecular and morphological data, Floridatrema Kinsella & Deblock, 1994 is synonymised with Maritrema Nicoll, 1907, Candidotrema Dollfus, 1951 with Pleurogenes Looss, 1896, and Schistogonimus Lühe, 1909 with Prosthogonimus Lühe, 1899. The taxonomic value of some morphological features, used traditionally for the differentiation of genera within the Lecithodendriidae and Prosthogonimidae, is reconsidered. Previous systematic schemes are discussed from the viewpoint of present results, and perspectives of future studies are outlined.     

Life cycle and identification of an eyefluke from Israel transmitted by Melanoides tuberculata (Müller, 1774)

A philophthalmid species from Israel using the freshwater snail Melanoides tuberculata as intermediate host was studied. The biological and morphological characteristics of all developmental stages of the life cycle of this philophthalmid were described, and compared to those of Philophthalmus lucipetus Rudolphi, 1819 from Israel, Philophthalmus gralli Mathis and Leger, 1910 from Jordan, Philophthalmus palpebrarum Looss, 1899, Philophthalmus nocturnus Looss, 1907, Cercaria distomatosa Looss 1896 from Egypt, and Philophthalmus lucknowensis Baugh, 1962 from India. The possible identity with 1 of these species is discussed. On the basis of comparative analysis of the data for all parasite stages in the life cycle, geographical distribution, snail hosts, and snail host specificity, we propose to designate the Israeli Melanoides tuberculata-transmitted eye fluke to Philophthalmus distomatosa n. comb. (Looss, 1896), (Digenea: Philophthalmidae).     

Reorganisation of the superfamily Lepocreadioidea Odhner, 1905 based on an inferred molecular phylogeny

Utilising phylogenetic estimates inferred from molecular sequences, the superfamily Lepocreadioidea Odhner, 1905 is re-organised, with the major family, the Lepocreadiidae, split into three separate families, the Lepocreadiidae Odhner, 1905, Aephnidiogenidae Yamaguti, 1934 and Lepidapedidae Yamaguti, 1958. These families have been widely recognised as subfamilies. Also recognised are the families Enenteridae Yamaguti, 1958, Gorgocephalidae Manter, 1966 and Gyliauchenidae Fukui, 1929. The constituent genera of these families are listed, some relying on molecular data and others on morphological similarity to molecularly-typed genera. Nine genera have not been placed in families and are considered incertae sedis.     

Morphology and diagnosis of the fourth-stage larva of <Emphasis Type="Italic">Coronocyclus labratus</Emphasis> (Looss, 1900) (Nematoda: Strongyloidea) parasitising equids

The fourth larval stage (L4) of Coronocyclus labratus (Looss, 1900) Hartwich, 1986, one of the common species of the Cyathostominae found in equids, is identified and described. The larvae found were identified as C. labratus by finding moulting forms possessing characters of both larval and adult stages. The larvae are similar to those of Cylicocyclus leptostomum (Kotlán, 1920) Foster, 1936, Cyathostomum catinatum Looss, 1900 and Cylicostephanus goldi (Boulenger, 1917) Lichtenfels, 1975. The buccal capsule (BC) wall of the L4 of Cylicocyclus leptostomum is thinner than that of Coronocyclus labratus, and the ring of the oesophageal funnel is comparatively less well developed. In C. labratus the dorsal tooth protrudes only slightly into the buccal cavity, and this larva possesses a characteristically elongate, pyriform oesophagus. In Cyathostomum catinatum, the BC walls are thicker than in Coronocyclus labratus, and the dorsal tooth is more bluntly pointed. Sublateral teeth, if present, are bluntly pointed in the former species, but usually absent or indistinct in C. labratus. Larvae of Cylicostephanus goldi differ from those of Coronocyclus labratus in the larger size of the BC.