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1.
Summary Falcaustra mackini (Walton, 1941) is redescribed. The anterior extremity is shown to be supported by three cordons arising from between the lips; the two subdorsal cordons are always curved on to the dorsal lip, whereas the ventral cordon curves on to either the right or left subventral lip. This cephalic morphology differs markedly from Falcaustra sensu stricto. F. mackini is designated type of Cordonema n. g. (Kathlaniinae). Cordonema cryptobranchi (Walton, 1930) n. comb. and C. variabilis (Walton, 1941) n. comb., both occurring in Cryptobranchus allegheniensis, the host for C. mackini, are included in the new genus. ac]19801207  相似文献   

2.
The Pseudoplagioporinae n. subf. (Opecoelidae) is proposed for species of Pseudoplagioporus Yamaguti, 1938, Fairfaxia Cribb, 1989, and Shimazuia Cribb, 2005, a small group of relatively distinctive, Indo-West Pacific taxa reliably known almost entirely from emperor fishes (Perciformes: Lethrinidae). These taxa were previously recognized in the Plagioporinae Manter, 1947, but that subfamily has recently been restricted to a clade of Holarctic, freshwater taxa, whereas analyses of new genetic data find the pseudoplagioporines to form a distinct clade among a larger assemblage of marine taxa. New material was sourced from fishes collected mainly in Queensland waters, Australia, but with some specimens from off Western Australia, the Northern Territory, and Japan. Orthodena tropica Durio & Manter, 1968 is transferred to Pseudoplagioporus as Ptropicus (Durio & Manter, 1968) n. comb., and Orthodena Durio & Manter, 1968 thus becomes a synonym of that genus. Three new species of Pseudoplagioporus are proposed. One, Pmediocris n. sp., like other species of Pseudoplagioporus, occurs in several species of Lethrinus. The other two new species, P. labiatus n. sp. and P. roseovulatus n. sp., apparently do not infect species of Lethrinus and were instead found only in the Bigeye emperor Monotaxis grandoculis (Forsskål) and the Redfin emperor M. heterodon (Bleeker), respectively. New host-locality combinations and the first genetic data, for the ribosomal ITS2 DNA region, and the 28S rRNA, 18S rRNA, and cox1 mtDNA genes, are reported for Pseudoplagioporus lethrini Yamaguti, 1938, Pinterruptus Durio & Manter, 1968, Ptropicus, Fairfaxia lethrini Cribb, 1989, Fairfaxia cribbi Hassanine & Gibson, 2005, and Shimazuia lethrini (Yamaguti, 1938) Cribb, 2005.  相似文献   

3.
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.  相似文献   

4.
Acleotrema Johnston & Tiegs, 1922 is resurrected and its diagnosis amended. A. girellae Johnston & Tiegs, 1922 is redescribed based on the lectotype from the Australian Museum (Sydney, Australia). A. kyphosi Yamaguti, 1968 is considered a junior synonym of A. girellae. Heteroplectanum Rakotofiringa, Oliver & Lambert, 1987 is considered a junior synonym of Acleotrema. The nine species of the latter genus are transferred to Acleotrema as: A. diplobulbus (Yamaguti, 1968) n. comb., A. nenue (Yamaguti, 1968) n. comb., A. spiculare (Yamaguti, 1968) n. comb., A. yamagutii (Oliver, 1983) n. comb., A. nenuoides (Rakotofiringa, Oliver & Lambert, 1987) n. comb., A. parastromatei (Rakotofiringa, Oliver & Lambert, 1987) n. comb., A. serrulopenis (Rakotofiringa, Oliver & Lambert, 1987) n. comb., A. tamatavense (Rakotofiringa, Oliver & Lambert, 1987) n. comb. and A. oliveri (León-Règagnon, Pérez-Ponce de León & Garcia- Prieto, 1997) n. comb. An historical account of the species of Acleotrema is presented.  相似文献   

5.
The similarities between Opecoelus Ozaki, 1925, Coitocaecum Nicoll, 1915, Opegaster Ozaki, 1928 and Paropecoelus Pritchard, 1966 and the difficulty of separating Opecoelus and Opegaster are discussed. It is proposed that Opegaster be reduced to synonymy with Opecoelus and the diagnosis of the latter amended to accommodate both forms. Four new species of Opecoelus are described from marine teleosts in Australian waters. These are Opecoelus woolcockae n. sp. from Acanthopagrus butcheri and A. australis from off South Australia, New South Wales and southern Queensland, O. pomatomi n. sp. from Pomatomus saltatrix off New South Wales, O. crowcrofti n. sp. from Atherinomorus ogilbyi off southern Queensland and O. queenslandicus n. sp. from Apogon fasciatus off southern Queensland. The following new combinations are formed: Opecoelus gonorhynchi (Gavrilyuk, 1979) n. comb., O. elongatus (Yamaguti, 1959) n. comb., O. pentadactylus (Manter, 1940) n. comb., O. apogonichthydis (Yamaguti, 1938) n. comb., O. cameroni (Caballero & Caballero, 1969) n. comb., O. dendrochiri (Yamaguti, 1970) n. comb., O. hawaiiensis (Yamaguti, 1970) n. comb., O. jamunicus (Srivastava, 1968) n. comb., O. longivesiculus (Yamaguti, 1952) n. comb., O. mastacembalii (Harshey, 1937) n. comb., O. mehrii (Harshey, 1937) n. comb., O. synodi (Manter, 1947) n. comb., O. tamori (Yamaguti, 1938) n. comb., O. bothi (Yamaguti, 1970) n. comb., O. caulopsettae (Manter, 1954) n. comb., O. beliyai (Pande, 1937) n. comb., O. brevifistulus (Ozaki, 1928) n. comb., O. cryptocentri (Yamaguti, 1958) n. comb., O. dactylopteri (Yamaguti, 1970) n. comb., O. dermatogenyos (Yamaguti, 1970) n. comb., O. ditrematis (Yamaguti, 1942) n. comb., O. gobii (Yamaguti, 1952) n. comb., O. hippocampi (Shen, 1982) n. comb., O. iniistii (Yamaguti, 1970) n. comb., O. lobulus (Wang, 1977) n. comb., O. macrorchis (Yamaguti, 1938) n. comb., O. parapristipomatis (Yamaguti, 1934) n. comb., O. pritchardae (Overstreet, 1969) n. comb., O. syngnathi (Yamaguti, 1934) n. comb., O. lutiani (Bravo-Hollis & Manter, 1957) n. comb., O. ovatus (Ozaki, 1928) n. comb., O. plotosi (Yamaguti, 1940) n. comb. and O. rectus (Ozaki, 1928) n. comb.; all the new combinations were previously species of Opegaster.  相似文献   

6.
Summary Chandlerella chitwoodae Anderson, 1961 (prevalence 65%), Splendidofilaria caperata Hibler, 1964 (21%), Eufilaria longicaudata Hibler, 1964 (15.5%), C. quiscali (von Linstow, 1904) Robinson, 1971 (1.9%), Cardiofilaria pavlovskyi Strom, 1937 (0.4%) and Splendidofilaria wehri (0.3%) were found in crows (Corvus brachyrhynchos brachyrhynchos Brehm) wintering in southern Ontario, Canada. S. caperata, E. longicaudata, Cardiofilaria pavlovskyi and S. wehri are reported for the first time from this host.Infection with Chandlerella chitwoodae and E. longicaudata produced microfilaraemias and these two common species apparently are maintained in the crow population. Infection with S. caperata was amicrofilaraemic (occult) and this common species cannot, therefore, be maintained in the crow population. C. quiscali, Cardiofilaria pavlovskyi and S. wehri occurred infrequently and must be common parasites of other woodland bird species. The presence of both common and sporadic infections in crows suggests that some avian filarioids parasitize numerous birds sharing a particular habitat. However, some host species are probably more important than others in maintaining infections within an avian community.The hosts of each species in Chandlerella, Splendidofilaria, Cardiofilaria and Eufilaria are listed. Chandlerella flexivaginalis (Jones, 1961) Sultana, 1962 and C. hispanica López-Caballero, 1974 are placed in synonymy with C. chitwoodae. Splendidofilarioides Freitas & Ibáñez, 1968 is made a synonym of Splendidofilaria and the type species becomes Splendidofilaria pachacuteci (Freitas & Ibáñez, 1968) n. comb. S. passerina Koch & Huizinga, 1971 is synonymized with S. algonquinensis (Anderson, 1955) Anderson, 1961. Pseudaproctella andersoni var. major Chabaud, Brygoo & Richard, 1964 and Cardiofilaria chabaudi Dissanaike & Fernando, 1965 are placed in synonymy with C. major Dissanaike & Fernando, 1965. Eufilaria cypseli (Annett, Dutton & Elliot, 1901) Nelson, 1966 is transferred to Lemdana as L. cypseli (Annett, Dutton & Elliot, 1901) n. comb. E. buckleyi (Desmukh, 1968) n. comb. is designated for Neofilaria buckleyi Desmukh, 1968 (= Eufilaria utae Anderson & Bain, 1976). ac]19800116Addendum: Since this paper went to press the following article has come to our attention: Olsen, O.W. & Braun, C.E. (1976) New species of Splendidofilaria and Chandlerella (Filarioidea: Nematoda), with keys to the species, from the band-tailed pigeon (Columba fasciata fasciata) in the Rocky Mountain region. Great Basin Naturalist, 36, 445–457. In their paper the authors describe the new species Splendidofilaria columbensis, S. hibleri and Chandlerella robinsoni. S. columbensis and S. hibleri are known from males only and their validity requires further study. C. robinsoni will also require further study.  相似文献   

7.
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.  相似文献   

8.
Summary A new species, Macvicaria taksengi (Opecoelidae: Plagioporinae), is described from the fishes Otolithes ruber and Sillago sihama from Pinang, Malaysia. It differs from most other members of the genus in the position of the ovary relative to the testes and the anterior position of the genital pore. A brief discussion on the Indo-West Pacific forms of the genus Macvicaria and related genera includes references to several new combinations: M. [Lebouria] isaitschikowi (Layman, 1930), M. [Plagioporus] sillagonis (Yamaguti, 1938), M. [Plagioporus] chrysophrys (Nagaty & Abdel Aal, 1969) and M. [Plagioporus (Plagioporus)] longisaccus (Fischthal & Kuntz, 1964).  相似文献   

9.
Problems in taxonomy of the Polymorphidae are discussed, with particular reference to trunk spines. Andracantha gen. n. is proposed for species with genital spines and 2 fields of trunk spines. Corynosoma gravida Alegret 1941, C. mergi Lundstro?m 1941 and C. phalacrocoracis Yamaguti 1939 are redescribed and placed in Andracantha, with A. gravida (Alegret, 1941) comb. n. designated as type species.  相似文献   

10.
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.  相似文献   

11.
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.  相似文献   

12.
13.
Neolebouria blatta n. sp. is described from Pristipomoides argyrogrammicus (Valenciennes) and Etelis carbunculus Cuvier in waters off New Caledonia. It differs from all other species of Neolebouria Gibson, 1976 but one, N. georgenascimentoi Bray, 2002, in the extension of the cirrus-sac to the ovary or nearly so. It differs from N. georgenascimentoi in its continuous, rather than interrupted, vitelline distribution. N. blatta belongs to a small group of similar Neolebouria species reported in deep-water lutjanids, which includes N. longisacculus (Yamaguti, 1970) n. comb., N. rooseveltiae (Yamaguti, 1970) n. comb. and N. ulaula (Yamaguti, 1970).  相似文献   

14.
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.  相似文献   

15.
Five species of philometrid nematodes (subfamily Philometrinae) are redescribed on the basis of newly collected materials from marine fishes from Japan. The species Philometra sciaenae Yamaguti, 1941, considered by Rasheed (1963) a synonym of P. lateolabracis (Yamaguti, 1935), is re-established as a valid species and the male of this nematode, collected from the ovary of the type-host, Argyrosomus argentatus, is described for the first time; the latter is characterised mainly by the length of equally long spicules (0.108–0.126 mm) and the length ratio of the gubernaculum and spicules (1:2.25). Other species redescribed on females include Philometra inimici Yamaguti, 1941 and P. sebastisci Yamaguti, 1941 from the ovary of their type-hosts, Inimicus japonicus and Sebastiscus marmoratus, respectively, and also Philometroides seriolae (Ishii, 1931) from the musculature of Seriola quinqueradiata (type-host), and Clavinema mariae (Layman, 1930) from the subcutaneous tissue of Pleuronectes schrenki and Acanthogobius flavimanus (a new host record). For the first time, cephalic ends of some of these species were studied under the scanning electron microscope (SEM) and the character of their cephalic papillae was described. The importance of a knowledge of male morphology for the taxonomy of philometrids is stressed.  相似文献   

16.
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.
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.
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17.
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.  相似文献   

18.
Four new species of Alaus Eschscholtz, 1829 are described: A. cinnamomeus n. sp., A. latlpennls n. sp., A. serlceus n. sp. and A. thoracopunctatus n. sp. Three species removed from Chalcolepldlus Eschscholtz, 1829, are transferred to this genus: A. allcll (Pjatakowa, 1941) n. comb., A. haroldl (Candèze, 1878) n.comb. and A. unlcus (Fleutiaux, 1910) n. comb. The characters of external morphology of these seven species and male and female genitalia, when available, are described and illustrated. An identification key for all species of the genus is included: A. allcll (Pjatakowa, 1941) n. comb., A. calcarlpllosus Casari, 1996, A. cinnamomeus n. sp., A. haroldl (Candèze, 1878) n. comb., A. latlpennls n. sp., A. lusclosus (Hope, 1832), A. melanops Leconte, 1863, A. myops (Fabricius, 1801), A. nobllls Sallé, 1855, A. oculatus (Linnaeus, 1758), A. patrlclus (Candèze, 1857), A. plebejus Candèze, 1874, A. serlceus n. sp., A. thoracopunctatus n. sp., A. tricolor (Olivier, 1790), A. unlcus (Fleutiaux, 1910) n. comb., A. veracruzanus Casari, 1996 and A. zunianus Casey, 1893.  相似文献   

19.
Lethrinitrema gibbus n. g., n. sp. and L. dossenus n. sp. are described from the fish Lethrinus rubrioperculatus Sato collected off New Caledonia, South Pacific. Members of Lethrinitrema n. g. (Ancyrocephalidae) are characterised by having two pyriform haptoral reservoirs and ventral anchors with lateral grooves. The elongate tubular distal end of each reservoir bifurcates, draining into a superficial lateral groove on each side of the ventral anchors. The haptoral reservoirs are postulated to store secretory products which assist in attachment to the host. Lethrinitrema spp. also possess tandem gonads, a male copulatory organ without an accessory piece or with thinly sclerotised accessory piece, and a dextrolateral, non-sclerotised vaginal bulb. The two new species have small, poorly demarcated haptors with small haptoral armament and a crown-like piece on the tip of the inner root of the ventral anchors. They differ from each other in the shape and size of the ventral bar and male copulatory organ (40–45 μm in length in L. gibbus vs 24–30 μm in L. dossenus). Three other species, previously included in Haliotrema Johnston & Tiegs, 1922, are transferred to Lethrinitrema, i.e. L. chrysostomi (Young, 1968) n. comb., L. fleti (Young, 1968) n. comb. (both briefly redescribed from paratypes) and L. lethrini (Yamaguti, 1937) n. comb. All species of Lethrinitrema parasitise Lethrinus spp. (Lethrinidae), and there is evidence for the existence of further Lethrinitrema spp. on Lethrinus spp. in the Indo-Pacific region.  相似文献   

20.
Summary Aviculariella alcyona Wehr, 1931 is redescribed on the basis of specimens from the gizzard of Megaceryle a. alcyon (L.) (Alcedinidae). Numerous characters are reported for the first time. The genus is distinguished from Rusguniella and Ingliseria by the presence of triangular cordons with an inner denticulate border, a prominent cephalic vesicle behind the cordons and simple deirids. The genus also contains: A. brevis (Maplestone, 1931) of Halcyon smyrnensis in India; A. alcedonis (Yamaguti & Mitunaga, 1943) of Alcedo atthis bengalensis in Taiwan; A. collaricephala (Oschmarin, 1959) of Alcedo atthis in the U.S.S.R.; A petterae Bain & Chabaud, 1965 of Corythornis vingtsioides (Turdidae) in Madagascar and A. alii (Rasheed, 1960) n. comb. of Ceryle radis leucomelanura in India; the last-named species may be a synonym of A. brevis. The status of some of these species requires further study. ac]19790421  相似文献   

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