Revision of the lygaeid genera Porta and Primierus (Hemiptera: Heteroptera), with the description of a new genus of Ozophorini from Papua New Guinea (Hemiptera)

Abstract. The lygaeid genera Porta Distant and Primierus Distant are revised and placed in the tribe Ozophorini. A key to all species is included. Phylogenetic relationships are discussed and a cladogram constructed. The following new species are described: Porta illustris (Philippines); P.longipes (Sabah), Primierus quadrispinosus (Sarawak, Sabah, Malaya), P.venustus (Sabah), and P.longirostris (Thailand). Gressittocoris intimidator is described as a new genus and species of Ozophorini from Papua New Guinea. Porta gracilis Distant is reported from Sabah, Sumatra and Thailand for the first time and records of P.gracilis from the Philippines are referred to Porta illustris sp.n. Illustrations include details of the genitalia and dorsal views of Primierus quadrispinosus, P.longirostris and Gressittocoris intimidator.     

The eyespots of the oncomiracidium of Euzetrema knoepffleri (Monogenea): ultrastructure and evolution during the life-cycle (author's transl)]

Euzetrema knoepffleri (Monogenea, Monopisthocotylea) is a parasite of the urinary bladder of Euproctus montanus (Amphibia, Urodela). The eyespots of the oncomiracidium of E. knoepffleri are rhabdomeric; each anterior pigmented cell has one rhabdomere, each posterior pigmented cell has two rhabdomeres. This pattern is quite similar to that of the eyespot of another Monopisthocotylea, Entobdella soleae but the lack of cristalline lens in E. knoepffleri appears as a new feature of the Monopisthocotylea. The symmetry of the pigmented structures seems to be effectively connected with the swimming mode of the larva. Moreover, the ultrastructural differences between the two species Euzetrema knoepffleri and Entobdella soleae may be in relation with their different behaviour concerning light. After the fixation of the larva on its host, the comparative study of the evolution of the eyespots, shows the disappearance of the cristalline lens in Entobdella, and the loss of rhabdomeric structures in Euzetrema. These differences seem related with the nature of the microbiotope of the adult: Entobdella soleae is a skin parasite, Euzetrema knoepffleri a reno-vesical one.     

Untersuchungen zur Taxonomie der Gattung Araniella (Araneae, Araneidae)

Morphological and ethological criteria were used in studying the taxonomic relations between different forms within the genus Araniella . Criteria for a diagnosis of all species and subspecies of the genus are given. A. opisthographa (Kulczyski, 1905), A. cucurbitina (Clerck, 1757), A. proxima (Kulczyski, 1885) and A. maderiana (Kulczyski, 1905) form one group of sibling species in the narrowest sense, A. alpica (L. Koch, 1869) and A. inconspicua (Simon, 1874) a second distinct one. A. displicata (Hentz, 1847) seems to occupy a relatively isolated position. A. cossoni (Simon, 1885) is regarded as a synonym for A. cucurbitina . It is impossible to make a statement about the status of A. silesiaca (Fickert, 1876) and A. croatica (Kulczyski, 1905) because of the lack of sufficient material. A. silesiaca is not a synonym for Araneus crispulus Tullgren, 1952, a species which does not belong to the genus Araniella .     

Morphological and molecular characterization of the marine-teleost parasitizing acanthocephalan Echinorhynchus hexagrammi (Syndermata: Palaeacanthocephala) from a new host,Liparis sp. (Actinopterygii: Scorpaeniformes)

Originally described from the masked greenling Hexagrammos octogrammus (Pallas, 1814), the palaeacanthocephalan Echinorhynchus hexagrammi Baeva, 1965 has so far been known from seven species in six families of marine teleosts distributed in the Sea of Okhotsk off Sakhalin and in the Northwestern Pacific off Hokkaido, Japan. In this study, we examined the phylogenetic position of E. hexagrammi based on material obtained from the intestine of an unidentified snailfish, Liparis sp., dredged in Akkeshi Bay, Hokkaido, Japan. We performed an analysis using two gene markers, the mitochondrial cytochrome c oxidase subunit I and the nuclear 28S rRNA, along with other sequences available in public databases. In the resulting tree, E. hexagrammi was more closely related to two species complexes, the E. bothniensis Zdzitowiecki and Valtonen, 1987 complex and the E. gadi Zoega in Müller, 1776 complex, rather than to E. brayi Wayland, Sommerville, and Gibson, 1999, E. cinctulus (Porta, 1905), E. salmonis Müller, 1784, and E. truttae Schrank, 1788. The morphology of the examined material herein identified as E. hexagrammi is briefly described. This study represents the first host record of E. hexagrammi from the snailfish family Liparidae.     

A review of the Arhythmacanthidae (Acanthocephala) with a description of Heterosentis hirsutus n. sp. from Cnidoglanis macrocephala (Plotosidae) in Australia

Heterosentis hirsutus n. sp. is described from Cnidoglanis macrocephala (Siluriformes: Plotosidae) from the Swan Estuary, Western Australia. It is distinguished by having 14 longitudinal rows of 6-7 hooks per row on the proboscis, a trunk armed anteriorly and posteriorly (= genital spines) with minute spines and lemnisci that may extend to the posterior margin of the proboscis receptacle. The new species also has prominent fragmented nuclei in its trunk wall. New information is given for Heterosentis plotosi Yamaguti, 1935 from Plotosus lineatus (Siluriformes: Plotosidae) and H. paraplagusiarum (Nickol, 1972) Amin, 1985 from Paraplagusia guttata (Pleuronectiformes: Cynoglossidae), both from Queensland. A key to the species of Heterosentis Van Cleave, 1931 is provided. The Arhythmacanthidae subfamilies are reviewed: there is little utility in the recognition of these taxa because of the small number of genera involved and the validity of the characters on which they are based is in doubt, particularly whether trunk spines are present or absent. Only Acanthocephaloides Meyer, 1932, Breizacanthus Golvan, 1969, Euzetacanthus Golvan & Houin, 1964, Heterosentis, Hypoechinorhynchus Yamaguti, 1939 and Paracanthocephaloides Golvan, 1969 of the Arhythmacanthidae are considered valid. A key to these genera is provided. The monotypic genus Neoacanthocephaloides Cable & Quick, 1954 is considered a new synonym of Acanthocephaloides thus creating Acanthocephaloides spinicaudatus (Cable & Quick, 1954) n. comb. Arhythmacanthus Yamaguti, 1935 is maintained as a synonym of Heterosentis because the distinction between two and three hook types is made equivocal when the transition between the apical and subapical hooks is gradual.     

Trypanosomes infecting cod Gadus morhua L. in the North Atlantic: a resurrection of Trypanosoma pleuronectidium Robertson, 1906 and delimitation of T. murmanense Nikitin, 1927 (emend.), with a review of other trypanosomes from North Atlantic and Mediterranean teleosts

Trypanosomes were isolated from Atlantic cod Gadus morhua L. collected from several fjords in western Norway. Morphological studies showed that the 12 infections studied represented a single species, identified as Trypanosoma pleuronectidium Robertson, 1906 which is resurrected and redescribed. This species is characterised by its body length (57.9 ± 5.4 μm), nearly central nucleus (NI = 1.05 ± 0.12) and relatively short post-kinetoplastic (PK) region (3.2 ± 0.8 μm). T. pleuronectidium is transmitted by the leech Calliobdella nodulifera (Malm). T. murmanense Nikitin, 1927 (emend.) is delimited to a species transmitted by the leech Johanssonia arctica (Johansson). This species is separated from T. pleuronectidium by its attained body length, more anterior nucleus, presence of cytoplasmic refractive granules, adnuclear vacuoles and by a longer PK region. Partial SSU rDNA sequences of T. pleuronectidium and T. murmanense from Norway (1980 nt) diverged by 1.9%. The nominal North Atlantic and Mediterranean trypanosome species are reviewed, and T. flesi Lebailly, 1904, T. bothi Lebailly, 1905 and T. limandae Brumpt & Lebailly, 1904 are considered synonyms of T. platessae Lebailly, 1904. T. triglae senegalensis Ranque, 1973 is not considered conspecific with T. triglae Neumann, 1909, and consequently raised to species status as T. senegalense Ranque, 1973. Some other likely synonymies are discussed. In addition to T. pleuronectidium and T. murmanense, the following marine teleost trypanosomes are provisionally listed as valid species pending further study: T. callionymi Brumpt & Lebailly, 1904; T. cotti Brumpt & Lebailly, 1904; T. delagei Brumpt & Lebailly, 1904; T. dorhni Yakimov, 1911; T. gobii Brumpt & Lebailly, 1904; T. laternae Lebailly, 1904; T. myoxocephali Fantham, Porter & Richardson, 1942; T. platessae Lebailly, 1904; T. scorpaenae Neumann, 1909; T. soleae Laveran & Mesnil, 1901; T. triglae Neumann, 1909; and T. yakimovi Yakimov, 1911.     

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).     

A revision of Lycodrilus phreodriloides (Oligochaeta, Tubificidae)

The taxon Lycodrilusphreodriloides Michaelsen, 1905 is fully described for the first time. It is now recognized as Baikalodrilus phreodriloides (Michaelsen) comb.n., a member of the Tubificidae. This is the last of the original Lycodrilus species to be reclassified.     

共系蚤属－新种及雌蚤－例畸形（蚤目：角叶蚤科）

鞋形共系蚤Ｓｙｎｇｅｎｏｐｓｙｌｌｕｓｃａｌｃｅａｔｕｓ（Ｒｏｔｈｓｃｈｉｌｄ,１９０５）自发表迄今８５年以来为一独模属。在峨眉山发现的一新种,是本属首次有了第二种。共系蚤属的地理分布也因新种的地理位置向北推到了西南区的西南山地亚区。新种雌蚤（配模）盲管的末端具一受精囊的雏形,认为这一结构在角叶蚤科的共系蚤属中的出现是一个返祖遗传性质的畸形。     

Moina oryzae n. sp. (Cladocera,Moinidae) from Tamil Nadu (South India)

Moina oryzae n. sp., from a rice field in South India, is described. The species is related toMoina reticulata Daday, 1905, and toMoina minuta Hansen, 1899. The parthenogenetic and sexual females and male are described. A differential diagnosis is given.     

Oschmarinella albamarina (Treshchev, 1968) n. comb., a liver fluke from the killer whale Orcinus orca (L.) off the British coast

Oschmarinella albamarina n. comb. is described from the bile-ducts of a killer whale Orcinus orca stranded on the British coast. The systematic position of the species is discussed in relation to the genera Campula Cobbold, 1858, Orthosplanchnus Odhner, 1905 and Oschmarinella Skrjabin, 1947, and the species is transferred from Orthosplanchnus to Oschmarinella. Campula rochebruni (Poirrier, 1886) is transferred to Oschmarinella, as O. rochebruni n. comb., and Oschmarinella mascomai Raga, 1986 is considered its synonym.     

Entobdella soleae--pointers to the future

The biology of the monogenean skin parasite Entobdella soleae and its relationship with its host, the common sole (Solea solea), are probably better known than those of any other monogeneans. The author describes his early involvement with this parasite and the special features of parasite and host that make this relationship so suitable for parasitological studies. Aspects of the biology of E. soleae that have been investigated are briefly mentioned, but most of the paper is concerned with areas of the parasite's biology that remain a challenge to determine. Unresolved areas are as follows: (1) the identity of the factor (or factors) in host skin mucus that stimulates hatching of the parasite's eggs; (2) whether or not the larvae of the parasite are attracted to their host; (3) the nature of factors controlling the contrasting behaviour of adult parasites on the upper and lower surfaces of the host; (4) how nutrients are supplied to the remote regions of the haptor; (5) whether the host has any control via its immune system over parasite invasion success and survival; (6) how the parasite copes with the migratory habits of some sole populations, assuming that such populations are infested with the parasite. The intimacy of this parasite/host relationship is its most remarkable feature, the reflection of which, not surprisingly, is the greatly restricted host range of the parasite. E. soleae has been reported from only three host species, all highly specialised bottom-dwelling members of Solea. It is all the more surprising that relatives of E. soleae, such as Neobenedenia melleni, retain the ability to parasitise an enormous range of hosts. How this versatility is achieved remains to be seen.     

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).     

Glossocercus chelodinae (MacCallum, 1921) n. comb. (Cestoda: Dilepididae) from freshwater turtles in Australia and a redefinition of the genus Bancroftiella Johnston, 1911

Glossocercus chelodinae (MacCallum, 1921) n. comb. is redescribed from fresh material recovered from the intestine of an Australian freshwater turtle, Chelodina expansa. G. chelodinae can be distinguished from all other species of the genus by the shape of its rostellar hooks. It is suggested that this species has colonised fish-eating turtles from fish-eating birds. The morphological relationships among Parvitaenia, Bancroftiella and Glossocercus are discussed. The diagnosis of Bancroftiella is amended and marsupials are eliminated as hosts. Bancroftiella sudarikovi Spasskii &; Yurpalova, 1970 becomes a synonym of Glossocercus glandularis (Fuhrmann, 1905); only B. tenuis Johnston, 1911, the type-species, and B. ardeae Johnston, 1911 remain in the genus.     

Characterization of ISR region and development of a PCR assay for rapid detection of the fish pathogen Tenacibaculum soleae

The aims of this work were to characterize the 16S-23S internal spacer region of the fish pathogen Tenacibaculum soleae and to develop a PCR assay for its identification and detection. All T.?soleae strains tested displayed a single internal spacer region class, containing tRNA(I) (le) and tRNA(A) (la) genes; nevertheless, a considerable intraspecific heterogeneity was observed. However, this region proved to be useful for differentiation of T.?soleae from related and non-related species. Species-specific primers were designed targeting the 16S rRNA gene and the internal spacer region region, yielding a 1555-bp fragment. Detection limit was of 1?pg DNA per reaction (相似文献   

Neoechinorhynchus (Neoechinorhynchus) chimalapasensis n. sp. (Acanthocephala: Neoechinorhynchidae) from the freshwater fish Awaous banana (Valenciennes) (Gobiidae) in Mexico

Neoechinorhynchus (Neoechinorhynchus) chimalapasensis n. sp. (Eoacanthocephala: Neoechinorhynchidae) is described from the intestine of Awaous banana (Valenciennes) (Pisces: Gobiidae) collected in the Río Negro, a tributary in the upper Río Coatzacoalcos basin, Santa María Chimalapa, Oaxaca State, Mexico. It is the third species of Neoechinorhynchus Stiles & Hassall, 1905 described from Mexican freshwater fishes, although 36 other species are known from freshwater fishes in the Americas. Like four other species of Neoechinorhynchus from freshwater fishes in North America and Mexico, N. (N.) limi Muzzall & Buckner, 1982, (N.) rutili (Müller, 1780) Stiles & Hassall, 1905, N. (N.) salmonis Ching, 1984 and N. (N.) roseus Salgado-Maldonado, 1978, males and females of the new species are less than 20 mm in length, lack conspicuous sexual dimorphism in size, have a small proboscis of about 0.1 mm in length with the largest hooks being the anteriormost, about 30–90 μm in length and of equal size, and have subequal lemnisci, larger than the proboscis receptacle but still relatively short and, in males, generally restricted to a position considerably anterior to the testes. The new species is closest to N. (N.) roseus, but it is distinguished from it by having: (1) a slightly larger cylindrical proboscis with almost parallel sides versus a globular proboscis with a rounded tip which is shorter and somewhat wider in N. (N.) roseus; (2) smaller but robust anterior proboscis hooks that do not reach the equatorial level or extend beyond the hooks of the middle circle as in N. (N.) roseus; and (3) the female gonopore situated ventrally subterminal, as opposed to being a significant distance anteriorly to the posterior extremity in N. (N.) roseus.     

Review of the Indo-Pacific scorpaenoid genus Plectrogenium Gilbert 1905 (Plectrogeniidae) with descriptions of eight new species

Ichthyological Research - A taxonomic review of Plectrogenium (Teleostei: Plectrogeniidae) disclosed 10 valid species, eight being new (most previously identified as P. nanum Gilbert 1905): P....     

Three species of Pagodia (Corynexochida,Trilobita) from the Furongian (Cambrian) of northern Anhui,China and their intraspecific variation

More than one thousand cranidia, librigenae, and pygidia of the trilobite Pagodia were collected from the Cambrian (upper Jiangshanian through Stage 10) at Fenghuangshan in northern Anhui, China. They were identified as Pagodia lotos Walcott, 1905, Pagodia depressa (Walcott, 1905), and Pagodia bia Walcott, 1905. Based on one rare nearly complete exoskeleton of P. depressa and comparisons among the three species of Pagodia, the redefinition for those species is attempted as follows. Pagodia lotos: Glabella rectangular, slightly convergent anteriorly; anterior border ridge-like, anterior border furrow deep; pygidium semicircular, axis tapered rearward, with 4 axial rings and a terminal piece. P. depressa: Cranidium subquadrate, highly convex; glabella cylindrical, convergent anteriorly; pygidium semicircular. P. bia: Glabella rectangular, constricted in the midlength; fixigena wide (tr.); anterior border very narrow (sag.) and ridge-like; pygidium semicircular with wide borders; pygidial axis ended closer to the pygidial border furrow. We also discuss their intraspecific variations, commonly seen on the exfoliated specimens: palpebral ridge evident or obliterated, the length (sag.) of anterior area variable, the decoration of exoskeleton surface (with granules variable in size, convex or pitted).