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.     

Adults and larvae of <Emphasis Type="Italic">Skrjabinocerca canutus</Emphasis> n. sp. (Nematoda: Acuariidae) from <Emphasis Type="Italic">Calidris canutus rufa</Emphasis> (Aves: Scolopacidae) on the southern Southwest Atlantic coast of South America

Adults and larvae of a new species of Skrjabinocerca Shikhobalova, 1930 (Nematoda: Acuarioidea) are described on the basis of light and scanning electron microscope studies. Specimens were recovered from Calidris canutus rufa Wilson (Aves: Scolopacidae) from the Southwest Atlantic coast of Uruguay. Data on the hosts, localities and main features of the four previously described species of the genus are provided. S. canutus n. sp. can be distinguished its congeners by a combination of the following characters: non-recurrent cordons, shorter right spicule and possession of a delicate finger-like projection on the distal end of the left spicule. S. prima Shikhobalova, 1930 has a left spicule which is stilletto-shaped and sharply pointed, S. europaea Wong & Anderson, 1993 has recurrent cordons, S. americana Wong & Anderson, 1993 possesses two delicate digitiform projections on the distal end of its left spicule and S. bennetti Bartlett & Anderson, 1996 has subequal spicules.     

Parapharyngodon osteopili n.sp. (Pharyngodonidae: Oxyuroidea) and a revision of Parapharyngodon and Thelandros

Summary Parapharyngodon osteopili n.sp. is described from the Cuban treefrog Osteopilus septentrionalis (Hylidae; Anura). Parapharyngodon Chatterji, 1933 and Thelandros Wedl, 1862 are redefined and distinguished on the basis of male and female caudal morphology and egg structure. Parapharyngodon spp. are found in insectivorous reptiles and amphibians whereas Thelandros spp. are essentially parasites of herbivorous and omnivorous reptiles. The following species are transferred to Parapharyngodon from Thelandros and represent new combinations: Parapharyngodon echinatus (Rudolphi, 1819), P. hemidactylus (Patwardhan, 1935), P. khartana (Johnston & Mawson, 1941), P. trachysauri (Johnston & Mawson, 1947), P. californiensis (read & Amrein, 1952), P. meridionalis (chabaud & Brygoo, 1962), P. mabouia (Rao & Hiregaudar, 1962), P. iguanae (Telford, 1965), P. calotis (Johnson, 1966), P. maculatus (Caballero, 1968) and P. garciae (Schmidt & Whittaker, 1975). Thelandros awokoyai (Babero & Okpala, 1962) n.comb., is transferred from Parapharyngodon. P. megaloon (Linstow, 1906) n.comb., P. seurati (Sandground, 1936) Freitas, 1957, P. waltoni (Read & Amrein, 1952) n.comb., P. cameroni (Belle, 1957) n.comb., P. aspiculus Khera, 1961, T. cinctus (Lonstow, 1897) and T. kuntzi Belle, 1957 are considered species inquirendae. ac]19810406     

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.     

Revision of the genus Diclidophora Krøyer, 1838 (Monogenea: Diclidophoridae), with the proposal of Macrouridophora n. g.

The present study re-examines the detailed morphology of the type-species, Diclidophora merlangi (Kuhn, in Nordmann, 1832) Krøyer, 1838, and other Diclidophora species parasitic on gadid fishes: D. denticulata (Olsson, 1876) Price, 1943, D. esmarkii (Th. Scott, 1901) Sproston, 1946, D. luscae (van Beneden & Hesse, 1863) Price, 1943, D. minor (Olsson, 1868) Sproston, 1946, D. palmata (Leuckart, 1830) Diesing, 1850, D. phycidis (Parona & Perugia, 1889) Sproston, 1946, D. pollachii (van Beneden & Hesse, 1863) Price, 1943 and the recently described D. micromesisti Suriano & Martorelli, 1984. An amended generic diagnosis of Diclidophora Krøyer, 1838 (synonym Diclidophora Diesing, 1850) is provided, which includes the presence of a prostatic vesicle in the terminal male genitalia and the distal fusion of the median and peripheral sclerites, a₁ and c₁ in the clamp anterior jaw. Macrouridophora n. g. is herein proposed for species previously considered in Diclidophora, which are parasitic on macrourid and morid fishes. The clamp morphology in Macrouridophora n. g. has distinct lamellate extension attachments to peripheral sclerites c₁ and the distal portion of d₁, with no distal fusion between a₁ and c₁ in the anterior jaw. Macrouridophora macruri (Brinkmann, 1942) n. comb. is chosen as the type-species. Nine other species are herein transferred to Macrouridophora n. g.: M. coelorhynchi (Robinson, 1961) n. comb., M. lotella (Machida, 1972) n. comb., M. nezumiae (Munroe, Campbell & Zwerner, 1981) n. comb. and M. tubiformis (Rohde & Williams, 1987) n. comb. are redescribed, based on the re-examination of type or voucher specimens. Macrouridophora attenuata (Mamaev & Zubtschenko, 1979) n. comb., M. caudata (Mamaev & Zubtschenko, 1984) n. comb., M. papilio (Mamaev & Avdeev, 1981) n. comb., M. paracoelorhynchi (Mamaev & Paruchin, 1979) n. comb. and M. physiculi (Mamaev & Avdeev, 1981) n. comb. have adequately described haptoral clamps in the literature. The clamp morphology in Macrouridophora sp. from Lepidorhynchus denticulatus in Australia is also considered. Diclidophora whitsonii Suriano & Martorelli, 1984 is herein transferred to the genus Macruricotyle Mamaev & Ljadov, 1975, as M. whitsonii (Suriano & Martorelli, 1984) n. comb. D. embiotocae Hanson, 1979 is herein considered a species incertae sedis. D. caudospina Khan & Karyakarte, 1983 and D. paddiforma Deo & Karyakarte, 1979 are herein considered species inquirendae. D. aglandulosa Deo, 1977, D. glandulosa Das, 1972, D. minuta Das, 1972 and D. spindale Deo, 1977 are formally dismissed as nomina nuda. The systematic position of Diclidophora Krøyer, 1838 and Macrouridophora n. g. in the subfamily Diclidophorinae Cerfontaine, 1895 (sensu Mamaev, 1976) is discussed.     

Named species and hosts of Sarcocystis (Protozoa: Apicomplexa: Sarcocystidae)

Summary A list is given of the present 93 species of the apicomplexan protozoan genus Sarcocystis together with their definitive and intermediate hosts (if known), synonyms, homonyms, lapsi calami, etc. The names of many species of this genus are poorly known, in doubt or controversial due to lack of access to some of the literature and to failure to accept the International Code of Zoological Nomenclature.The following taxonomic innovations are introduced: New species—S. nontenella for S. tenella Eble, 1961 [non] S. tenella (Railliet, 1886) from the buzzard Buteo buteo; S. scotti for Sarcocystis sp. from the housemouse completing its sexual development in the tawny owl, Strix aluco (see Tadros & Laarman, 1980); New combinations—S. ctenosauris for Cryptosporidium ctenosauris Duszynski, 1969 from the lizard Ctenosaura similis; S. lampropeltis for Cryptosporodium lampropeltis Anderson, Duszynski & Marquardt, 1968 from the king snake Lampropeltis c. calligaster; S. roudabushi for Isospora roudabushi Pellérdy, 1974 from the gopher snake Pituophis s. sayi; and S. tropicalis for Isospora tropicalis Mukherjea & Krassner, 1965 from the golden jackal Canis aureus.Supported in part by National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland research grant AI15367.Supported in part by National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland research grant AI15367.     

Long-term dynamics of population density and species composition of pasture ixodid ticks (Parasitiformes,Ixodidae) in anthropogenic and natural areas

Long-term monitoring of population density and species composition of ixodid ticks inhabiting the territory of Tomsk and its outskirts has demonstrated that at least two species (Ixodes persulcatus and I. pavlovskyi) simultaneously inhabit all the biotopes examined. It was found that the fraction of I. pavlovskyi increased in biotopes adjacent to city buildings. I. persulcatus dominated in natural control biotopes, whereas I. pavlovskyi were found in these biotopes as solitary specimens. It was demonstrated that during 15 years of observation (1996–2011), the population density of ticks in the outskirts significantly increased. The combination of ecological and chemical methods of tick control in limited territories can result in a noticeable decrease of tick population density. Two tick species non-typical of the region (Dermacentor reticulatus and Haemaphysalis concinna) were revealed in one biotope.     

Reclassification of Oxysomatium inglisi Anderson, 1964 and Aplectana gigantica olsen, 1938 (nematoda:Cosmocercoidea) from north American frogs

Summary Aplectana gigantica Olsen, 1938 and Oxysomatium inglisi Anderson, 1964 (Cosmocercidae) have been re-examined. Study of cephalic, oesophageal and male caudal structures and of the egg demonstrates that both species belong in the Kathlaniidae and they are reclassified as Falcaustra inglisi (Anderson, 1964) n. comb. and Megalobatrachonema gigantica (Olsen, 1938) n. comb. The genus Megalobatrachonema Yamaguti, 1941 is divided into M. (Megalobatrachonema) n. subg. (with M. nipponica Yamaguti, 1941 and M. gigantica) and M. (Chabaudgolvania) n. subg. (with M. campanae Chabaud & Golvan, 1959 and M. terdentatum (Linstow, 1898)). M. (Chabaudgolvania) lacks oesophageal valves which are present in M. (Megalobatrachonema). It is suggested that F. inglisi and M. gigantica illustrate a trend in the evolution of the Kathlaniinae towards reduction of cephalic support structures and simplification of the oesophagus to a club-shaped form lacking valves. An evolutionary hypothesis linking the Kathlaniinae to the Quimperiidae (Seuratoidea) is presented. The genus Chabaudinema Díaz-Ungría, 1968 is synonymized with Spectatus Travassos, 1923 and its type species is designated Spectatus americana (Díaz-Ungría, 1968) n. comb. ac]19791109     

Towards a natural classification of the subtribe Philonthina (Coleoptera: Staphylinidae: Staphylinini): a phylogenetic analysis of the Neotropical genera

Philonthina, the largest subtribe of the rove beetle tribe Staphylinini, is a hyperdiverse group in the Neotropical Region, accounting for about half of the genera of the subtribe. Despite such diversity, Neotropical Philonthina have never been analysed phylogenetically, deterring formulation of a modern classification of the Staphylinini. A cladistic analysis of Neotropical Philonthina was performed based on 110 morphological characters and 77 terminal taxa. Representatives of Philonthina from other regions and other main lineages of Staphylinini, Arrowinini and Platyprosopini were included to test their relationships with Neotropical Philonthina. The major results are the monophyly of 11 of the 17 endemic Neotropical genera of Philonthina, the placement of Holisus Erichson (Hyptiomina) into this clade showing a sister group relationship to myrmecophile genera, and the position of Erichsonius Fauvel outside of Philonthina within Staphylinini. Six of the current seven species of Endeius Coiffait & Sáiz group with Neotropical species of Philonthus Stephens. The separation of Gondwana about 65 my and major landscape modifications in the vast interior of northern South America during the past 25 my is proposed to explain the evolution of the endemic Neotropical genera of Philonthina. The following taxonomic changes are proposed: Erichsonius Fauvel, 1874 now placed as incertae sedis in Staphylinini; Endeius Coiffait & Sáiz, 1968, n.syn. of Philonthus Stephens, 1929 and Endeius nitidipennis (Solier, 1849) placed as incertae sedis in Philonthina. The following new combinations are proposed: Philonthus franzi (Sáiz, 1971), comb.n. , Philonthus loensis (Coiffait & Sáiz, 1968), comb.n. , Philonthus lugubris (Sáiz, 1971), comb.n. , Philonthus ovaliceps (Coiffait, 1981), comb.n. , Philonthus punctipennis (Solier, 1849), comb.res. and Philonthus subpunctipennis (Coiffait & Sáiz, 1968), comb.n. Philonthus herberti, n.nov., is proposed for Philonthus franzi Schillhammer, 1998 , which is a junior secondary homonym of Philonthus franzi (Sáiz, 1971).     

<Emphasis Type="Italic">Orstomella yaliuensis</Emphasis> n. sp., a xarifiid copepod (Crustacea) parasitic in the polyps of hump coral <Emphasis Type="Italic">Porites lutea</Emphasis> Milne Edwards &; Haime off Taiwan

A new species of xarifiid copepod, Orstomella yaliuensis n. sp., is described. It was found living in the polyps of a scleractinian coral, Porites lutea Milne Edwards & Haime, collected off Yaliu in the northern part of Taiwan. The new species can be distinguished from its two congeners, O. faviae Humes & Ho, 1968 and O. lobophylliae Humes & Ho, 1968, by the presence of five (rather than six) segments on the antennule, a spine only (rather than a seta and a spine) at the tip of the antenna, a uniramous leg 2, and a relatively long (rather than short) spine at the tip of the caudal ramus.     

Chromosome differences in Peromyscus maniculatus populations at different altitudes in Colorado

Mice of the genus Peromyscus all have 48 chromosomes. Yet the appearance of the 48 chromosomes is highly variable from species to species (Hsu & Arrighi, 1966, 1968, 1971; Pathak et al., 1973) and even in different populations of the same species (Sparkes & Arakaki, 1966; Ohno et al., 1966; Hsu & Arrighi, 1968; Arakaki et al. 1970; Te & Dawson, 1971; Bradshaw & Hsu, 1972; Murray & Kitchin, 1976). The evolutionary significance of this variation and the mechanisms for its initiation and maintenance have been of interest for quite a few years. However, it was not until the sophisticated chromosome banding techniques became available that mammalian cytogeneticists were able to begin to study the chromosome variation of Peromyscus in some detail. The use of C-banding led Hsu & Arrighi (1971) to the finding that the short arms of chromosomes in three different species of Peromyscus contained constitutive heterochromatin. These results suggested that the variations in the number of acrocentric chromosomes in Peromyscus might be a result of different amounts of heterochromatin. Later studies (Duffey, 1972; Waterbury, 1972; and Pathak et al., 1973) were also consistent with this hypothesis.However, it was soon discovered that not all chromosomal differences among Peromyscus populations are due to heterochromatin changes. Studies by Arighi et al. (1976) and Murray & Kitchin (1976) showed that some chromosomal differences between species and subspecies of Peromyscus are due to pericentric inversions. Thus, it appears that both inversions and the addition of heterochromatin are involved in the evolution of the karyotype of Peromyscus.The purpose of our study was to investigate the chromosomes of Peromyscus maniculatus in different populations in Colorado (U.S.A.) and to test for relationships involving an altitudinal gradient. In the first part of this study, orcein stained chromosomes from three subspecies of mice sampled at nine different altitudes were examined for karyotype variability. In the second part of the study, karyotypes of two subspecies (P. m. rufinus and P. m. luteus), representing high and low altitude populations were examined with Q banding to determine the mechanisms responsible for chromosomal differences.     

New,known and unidentified species of Eulimdana (Nematoda): additional information on biologically unusual filarioids of charadriiform birds

Eulimdana spp. were found in 13 of 32 species of charadriiform birds from North America and Iceland; 88 of 636 adult birds and seven of 72 juvenile birds harboured infections. Described are: E. andersoni n. sp. from Chlidonias niger; E. metcalforum n. sp. from Sterna hirundo; E. sonini n. sp. from Charadrius hiaticula; E. wongae n. sp. from Limosa fedoa; and E. bainae n. sp. from Numenius phaeopus. Eulimdana asperum Bartlett, Anderson, & Bush, 1989 is reported for the second time in its type-host, Phalaropus tricolor. The emerging pattern of one parasite species to one host species suggests that most Eulimdana species are strongly host specific. However, E. florencae Bartlett & Anderson, 1990 is reported for the first time in a second species of Calidris (C. alba) and may be the unidentified species found in C. bairdii, C. alpina and C. pusilla. Other unidentified species were found in Larus pipixcan, Arenaria interpres and Recurvirostra americana. A key to species-groups (three are proposed) and species of Eulimdana in charadriiforms is given. Two pieces of evidence support an earlier suggestion that infections are acquired by neo-natal charadriiforms: (1) the presence of E. wongae in a bird captured as a chick and examined after two months in captivity; and (2) a greater frequency of mixed sex infections with microfilariae in infected juvenile birds (four of seven) than in infected adult birds (five of 88). The latter also supports an earlier suggestion that post-reproductive worms are ephemeral.     

Microcotyle visa n. sp. (Monogenea: Microcotylidae), a gill parasite of Pagrus caeruleostictus (Valenciennes) (Teleostei: Sparidae) off the Algerian coast,Western Mediterranean

Parasite biodiversity of fish of the southern part of the Mediterranean sea is still incompletely explored. We describe here Microcotyle visa n. sp. from the gill filaments of the bluespotted seabream Pagrus caeruleostictus (Valenciennes) (Sparidae) collected off the Algerian coast. The identity of fish hosts was confirmed by barcoding. Microcotyle visa n. sp. is herein described and illustrated. Analysis of the cox1 gene of the monogeneans revealed minor intraspecific variation (1.4%), an order of magnitude lower than the distance between this species and other Microcotyle species (10–15 %). Microcotyle visa n. sp. is distinguished from Microcotyle erythrini van Beneden & Hesse, 1863, a congener infesting sparids, on the basis of morphological (size of clamps, number of testes) and molecular (cox1) differences. This is the fourth member of the genus known to parasitise a sparid host. A species of Paramicrocotyle sp. included in the molecular analysis was nested within a robust Microcotyle + Paramicrocotyle clade; in the absence of demonstrated molecular and morphological differences, we consider that Paramicrocotyle Caballero & Bravo-Hollis, 1972 is a junior synonym of Microcotyle van Beneden & Hesse, 1863 and transfer two species of Paramicrocotyle as Microcotyle danielcarrioni (Martinez & Barrantes, 1977) n. comb. and Microcotyle moyanoi (Villalba & Fernandes, 1986) n. comb.

     

Fern sporophagy in Coleoptera from the Juan Fernandez Islands,Chile, with descriptions of two new genera in Cryptophagidae and Mycetophagidae

Abstract. Fern sporophagy is reported in species of Cryptophagidae, Mycetophagidae and Anthribidae occurring on the Juan Fernandez Islands, Chile. The following taxa are described and/or discussed: Cryptophagidae: Cryptothelypterus gen.n., with five species: C.obrieni sp.n., C.pteropilosus sp.n., C.selkirki (Bruce) comb.n., C.skottsbergi (Bruce) comb.n., and C.splendens (Bruce) comb.n.; Mycetophagidae: Filicivora gen.n., with one species, F.chilensis (Philippi & Philippi) comb.n.; and Anthribidae: Opisolia lenis Jordan. A key to the species of Cryptothelypterus is provided. Convergent adaptations for fern sporophagy in these groups are discussed, hypotheses are given for the evolution of this habit, and comments are made on wing atrophy.     

Beitrag zur systematik vonScilla L. subgen.Scilla (inklusiveChionodoxa Boiss.)

Zusammenfassung Die vonBoissier aufgestellte GattungChionodoxa wird auf Grund samenanatomischer und karyologischer Befunde eingezogen. Ihre nahe Verwandtschaft mitScilla bifolia agg. konnte aufgezeigt werden. Die wesentlichen Unterschiede derScilla bifolia- Gruppe (inklusiveChionodoxa-Arten) zu anderen Gruppen myrmekochorerScilla-Arten sowie zuPuschkinia undHyacinthus wurden dargelegt.Folgende neue Kombinationen werden aufgestellt:Scilla luciliae (Boiss.)Speta comb. nova,Scilla cretica (Boiss. &Heldr.)Speta comb. nova,Scilla nana (Schult. fil.)Speta comb. nova,Scilla sardensis (Barr &Sugden)Speta comb. nova,Scilla siehei (Stapf)Speta comb. nova,Scilla×allenii (Nicholson)Speta comb. nova.Weiters wurden die Chromosomenzahlen für einigeScilla- Arten überprüft und dabei fürScilla bifolia neben der bekannten diploiden auch die tetraploide Zahl 2n=36 aufgefunden.

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Summary The genusChionodoxa set up byBoissier is withdrawn due to seedanatomical and caryological statements and its species are incorporated intoScilla L. The close affinity between formerChionodoxa-species andScilla bifolia agg. could be demonstrated. The essential differences between theScilla bifolia group (including the formerChionodoxa species) and other groups of myrmecochorousScilla species,Puschkinia andHyacinthus were shown. The following new combinations are set up:Scella luciliae (Boiss.)Speta comb. nova,Scilla cretica (Boiss. &Heldr.)Speta comb. nova,Scilla nana (Schult. fil.)Speta comb. nova,Scilla sardensis (Barr &Sugden)Speta comb. nova,Scilla siehei (Stapf)Speta comb. nova,Scilla×allenii (Nicholson)Speta comb. nova.Furthermore the chromosome numbers of someScilla species were checked, and inScilla bifolia L. besides the known diploid number the tetraploid number 2n=36 was discovered.

     

Revision of Parancylodiscoides Caballero y C. & Bravo-Hollis, 1961 (Monogenoidea: Dactylogyridae), with a redescription of P. longiphallus (MacCallum, 1915) from the Atlantic spadefish Chaetodipterus faber (Broussonet) (Acanthuroidei: Ephippidae) in the Gulf of Mexico

The generic diagnosis of Parancylodiscoides Caballero y C. & Bravo-Hollis, 1961 (Monogenoidea: Dactylogyridae), with three valid species, was amended to include dactylogyrids having: a haptor with dorsal and ventral anchor/bar complexes, 14 hooks (seven pairs) and four reservoirs (two pairs); a dorsal bar with bifurcate ends; hooks with protruding, blunt and slightly depressed thumbs and undilated shanks; a dextroventral vaginal aperture leading to an elongate and oblique vaginal vestibule; a germarium dextral to the testis; a vas deferens looping the left intestinal caecum; a copulatory complex lacking an accessory piece; and two intestinal caeca lacking diverticula and united posterior to the gonads. Parancylodiscoides is most similar to Sundatrema Lim & Gibson, 2009, from which it differs only by the position of the vaginal aperture (sinistroventral in Sundatrema spp.) and by lacking a sucker-like genital pore. New information concerning the number and distribution of haptoral hooks, the relative positions of the gonads and the course of the vas deferens was provided for the type-species, P. chaetodipteri Caballero y C. & Bravo-Hollis, 1961. Parancylodiscoides longiphallus (MacCallum, 1915) Lim & Gibson, 2009 was redescribed based on specimens collected from the Atlantic spadefish Chaetodipterus faber from the Gulf of Mexico off Mississippi and Guaratuba Bay, Paraná, Brazil; its occurrence on the Atlantic spadefish from the Gulf of Mexico, Guaratuba Bay and off Puerto Rico represented new geographical records for this helminth. Parancylodiscoides caballerobravorum Cezar, Luque & Amato, 1999 was considered a junior subjective synonym of P. longiphallus. The monotypic Isohaliotrema Young, 1968 was placed in synonymy with Parancylodiscoides and its type-species, I. platacis Young, 1968, transferred to Parancylodiscoides as Parancylodiscoides platacis (Young, 1968) n. comb.     

Taxonomic notes on some species of the Cercospora complex (VI)

The new species Cercosporella pergulariae sp. nov., Pseudocercospora catalpicola sp. nov., Sirosporium rhamnigenum sp. nov., and Spiropes desmodiicola sp. nov. are described and Cercospora commelinicola Chupp is validated. Cercostigmina curta (Syd.) comb, nov., Eriocercosporella vitis-heterophyllae (Henn.) comb, nov., Mycovellosiella lactucae (Henn.) comb, nov., M. trichostemmatis (Henn.) comb, nov., M. tylophorae (Hansf.) comb, nov., Passalora caespitosa (Ellis & Everh.) comb, nov., P. chionanthi (Ellis & Everh.) comb, nov., Prathigada condensata (Ellis & Kellerm.) comb, nov., Pseudocercospora carrii (Barthol.) comb, nov., P. glaucescens (G. Winter) comb, nov., P. pamelae-ellisiae (G.P. Agarwal & N.D. Sharma) comb, nov., Pseudophaeoramularia angolensis (T. Cavalho &O. Mendes) comb, nov., Sporidesmium seminale (Ellis & Everh.) comb, nov., and Stenella praelonga (Syd.) comb. nov. are introduced. Cercospora litseae Henn. is reduced to synonym with Mycovellosiella litseae Meenu et al., and a second collection of Cercosporella indica from Vietnam is recorded.     

Molecular data reveal convergent reproductive strategies in iceryine scale insects (Hemiptera: Coccoidea: Monophlebidae), allowing the re-interpretation of morphology and a revised generic classification

Abstract The scale insect tribe Iceryini (Coccoidea: Monophlebidae) is a group of relatively large and polyphagous insects found worldwide. Currently, the tribe contains about 80 named species placed in seven genera, which are diagnosed largely on features associated with egg protection. We reconstruct the phylogeny of the Iceryini on the basis of nucleotide sequence data from nuclear ribosomal (18S and D2, D3 and D10 regions of 28S) and protein‐coding (histone H3) gene regions of 40 iceryine species representing six of the seven genera and seven outgroup taxa, mostly from two other tribes of Monophlebidae. Bayesian and maximum parsimony analyses recover a monophyletic tribe and clades that correspond more to geography than to the existing morphology‐based classification. Gueriniella Fernald is sister to the rest of the Iceryini and the genera Crypticerya Cockerell, Icerya Signoret and Steatococcus Ferris are not monophyletic. Our data imply that the distinctive iceryine reproductive strategies, such as protecting eggs in a waxy ovisac or inside a marsupium, are poor indicators of relationships. On the basis of molecular relationships and the re‐examination of morphological characters, we recognize only five genera of Iceryini –Crypticerya, Echinicerya Morrison, Gigantococcus Pesson & Bielenin, Gueriniella and Icerya – and substantially revise the generic concepts of Crypticerya, Gigantococcus and Icerya. We provide a key to the genera based on adult females. We redescribe and illustrate the adult female and first‐instar nymph of the type species Crypticerya rosae (Riley & Howard), Echinicerya anomala Morrison, Gigantococcus maximus (Newstead) (adult female only), Gueriniella serratulae (Fabricius) and Icerya seychellarum (Westwood). We recognize Auloicerya Morrison as a junior synonym ( syn.n. ) of Icerya, and transfer the two Auloicerya species to Icerya as I. acaciae (Morrison & Morrison) comb.n. and I. australis Maskell comb.rev. We recognize Steatococcus and Proticerya Cockerell as junior synonyms ( syn.n. ) of Crypticerya. From Steatococcus, we transfer five species to Crypticerya [C. mexicana Cockerell & Parrott comb.rev. , C. morrilli (Cockerell) comb.n. , C. tabernicola (Ferris) comb.n. , C. townsendi Cockerell comb.rev. , C. tuberculata (Morrison) comb.n. ], four species to Gigantococcus [Gi. euphorbiae (Brain) comb.n. , Gi. gowdeyi (Newstead) comb.n. , Gi. madagascariensis (Mamet) comb.n. , Gi. theobromae (Newstead) comb.n. ] and three species to Icerya [I. assamensis (Rao) comb.n. , I nudata Maskell comb.rev. , I. samaraia (Morrison) comb.n. ]. From Icerya, we transfer 14 species to Crypticerya [C. brasiliensis (Hempel) comb.n. , C. colimensis (Cockerell) comb.n. , C. flava (Hempel) comb.n. , C. flocculosa (Hempel) comb.n. , C. genistae (Hempel) comb.n. , C. littoralis (Cockerell) comb.n. , C. luederwaldti (Hempel) comb.n. , C. minima (Morrison) comb.n. , C. montserratensis (Riley & Howard) comb.n. , C. palmeri (Riley & Howard) comb.n. , C. rileyi (Cockerell) comb.n. , C. similis (Morrison) comb.n. , C. subandina (Leonardi) comb.n. , C. zeteki (Cockerell) comb.n. ] and nine species to Gigantococcus [Gi. alboluteus (Cockerell) comb.n. , Gi. bimaculatus (De Lotto) comb.n. , Gi. brachystegiae (Hall) comb.n. , Gi. longisetosus (Newstead) comb.n. , Gi. nigroareolatus (Newstead) comb.n. , Gi. pattersoni (Newstead) comb.n. , Gi. schoutedeni (Vayssière) comb.n. , Gi. splendidus (Lindinger) comb.n. , Gi. sulfureus (Lindinger) comb.n. ]. From Crypticerya, we transfer seven species to Icerya [I. clauseni (Rao) comb.n. , I. jacobsoni Green comb.rev. , I. jaihind (Rao) comb.n. , I. kumari (Rao) comb.n. , I. mangiferae (Tang & Hao) comb.n. , I. natalensis (Douglas) comb.rev. , I. nuda Green comb.rev. ] and five species to Gigantococcus [Gi. bicolor (Newstead) comb.n. , Gi. cajani (Newstead) comb.n. , Gi. caudatus (Newstead) comb.n. , Gi. ewarti (Newstead) comb.n. , Gi. rodriguesi (Castel‐Branco) comb.n. ]. Both I. hyperici (Froggatt) and Palaeococcus dymocki (Froggatt) are syn.n. of I. nudata (all previously placed in Steatococcus). We recognize I. maynei Vayssière as a syn.n. of Gi. nigroareolatus, I. tremae Vayssière as a syn.n. of Gi. schoutedeni and I. townsendi plucheae Cockerell as a syn.n. of C. townsendi. We revalidate the species name I. crocea Green stat.reval. In addition, we transfer I. taunayi Hempel to Laurencella Foldi (Monophlebidae: Llaveiini) as L. taunayi (Hempel) comb.n. Four species, Coccus hirticornis Boyer de Fonscolombe, I. chilensis Hempel, I. insulans Hempel and I. paulista Hempel, are considered incertae sedis. We designate lectotypes for C. rosae, E. anomala and I. candida (a junior synonym of I. seychellarum). Following this revision, we recognize 74 species of Iceryini, distributed as follows: 22 in Crypticerya, one in Echinicerya, 19 in Gigantococcus, two in Gueriniella and 30 in Icerya.     

Diplectanids infesting the gills of the barramundi Lates calcarifer (Bloch) (Perciformes: Centropomidae), with the proposal of Laticola n. g. (Monogenoidea: Diplectanidae)

Four species of the Monogenoidea, Laticola lingaoensis n. sp., L. latesi (Tripathi, 1957) n. comb. [previously Pseudorhabdosynochus latesi (Tripathi, 1957) Kritsky & Beverley-Burton, 1986], L. paralatesi (Nagibina, 1976) n. comb. [previously Diplectanum paralatesi Nagibina, 1976] and Diplectanum penangi Liang & Leong, 1991, are reported from the gills of Lates calcarifer (Centropomidae) from the South China Sea (new geographical records for L. latesi and D. penangi). Collections from off Bathurst Island, Northern Territory, Australia, represent a new geographic record for L. paralatesi; Chilka Lake, Orissa, India, is established as the type-locality for L. latesi. Laticola n. g. (Diplectanidae) is proposed for species with a spoon-shaped copulatory organ with two to four concentric incomplete ridges in the base. Laticola lingaoensis, the type-species of Laticola, is described, and L. latesi and L. paralatesi are redescribed based on specimens from the South China Sea. Pseudorhabdosynochus monosquamodiscusi Balasuriya & Leong, 1995 and Pseudorhabdosynochus yangjiangenesis Wu & Li, 2005 are considered junior subjective synonyms of L. latesi and L. paralatesi, respectively.