A review of the subgenus <Emphasis Type="Italic">Carpelimus</Emphasis> s. str. (Coleoptera,Staphylinidae) from tropical Africa

A review of the subgenus Carpelimus (s. str.) from tropical Africa is given. The subgenus includes 10 species. A new species C. uhligi sp. n. is described, neotype of Trogophloeus insularis, Kraatz 1858 is designated. T. aequithorax Bernhauer, 1932 is placed in synonymy with C. dieganus (Fauvel, 1904); T. oculatus Wollaston, 1865 and T. meridioafricanus Scheerpeltz, 1974, with C. insularis (Kraatz, 1858), T. rudebecki Scheerpeltz, 1974 with C. memnonius (Erichson, 1840); T. yemenicus Coiffait, 1981 with C. niloticus (Erichson, 1840); T. nigerrimus Coiffait, 1935 and T. mimus Cameron, 1945, with C. rufitarsis (Fauvel, 1907); and T. bredoi Bernhauer, 1943, with C. transmarinus (Fauvel, 1907). Lectotypes of T. aequithorax, T. calidus, T. nigerrimus, and T. bredoi are designated. Twenty species are transferred from the genus Carpelimus, and the following new combinations are formed: Thinodromus brincki Scheerpeltz, 1972; Th. montiumdraconis Scheerpeltz, 1974; Th. rhodesianus Scheerpeltz, 1974; and Th. sudanensis Scheerpeltz, 1974 comb. nn.). The initial generic placement of Carpelimus luzidus Cameron, 1944 is restored.     

Composition of the subgenus <Emphasis Type="Italic">Zeugotaenia</Emphasis>, genus <Emphasis Type="Italic">Chrysolina</Emphasis> (Coleoptera,Chrysomelidae), and examination of the nomenclatural types

Zeugotaenia Motschulsky, 1860 is resurrected as a valid name for the subgenus of Chrysolina with the type species Chrysomela limbata Fabricius, 1775. Diagnosis of the subgenus is compiled. Neotypes of Chrysomela limbata and Ch. limbifera Küster, 1846, and lectotypes of Chrysomela findelii Suffrian, 1851, Ch. hochhuthii Suffrian, 1851, and Ch. discipennis Faldermann, 1835 are designated. The types of Chrysomela limbata jenisseiensis Breit, 1920 and Chrysolina limbata kavani Bechyné, 1950 and the topotypes of Chrysomela limbata luigionii Depoli, 1936 are examined. Chrysolina furva Peyerimhoff, 1926 and Ch. dohrnii Fairmaire, 1865 do not belong to the subgenus Zeugotaenia.     

A review of the genus <Emphasis Type="Italic">Deporaus</Emphasis> (Coleoptera,Rhynchitidae) from the Russian fauna: 1. Subgenera <Emphasis Type="Italic">Pseudapoderites</Emphasis> and <Emphasis Type="Italic">Japonodeporaus</Emphasis>

The genus Deporaus from the Russian fauna is revised. Four species (D. pacatus, D. azarovae, D. septentrionalis, and D. hartmanni) of the subgenera Pseudapoderites and Japonodeporaus are found. Keys to the subgenera and to the species of the subgenus Pseudapoderites are given. The genus Deporaus, subgenera Pseudapoderites and Japonodeporaus, and four species are redescribed. The distribution of these species in Russia is discussed.     

A review of the genus <Emphasis Type="Italic">Deporaus</Emphasis> (Coleoptera,Rhynchitidae) from the Russian fauna: 2. Subgenera <Emphasis Type="Italic">Roelofsideporaus</Emphasis> and <Emphasis Type="Italic">Deporaus</Emphasis>

The subgenera Roelofsideporaus and Deporaus s. str. of the genus Deporaus with four species (D. affectatus, D. unicolor, D. nidificus, and D. betulae) recorded from the Russian fauna are revised. Keys to the species of the subgenus Roelofsideporaus and to the females of the subgenera Roelofsideporaus and Deporaus s. str. are given. The distribution of D. nidificus in Russia is not confirmed.     

A review of the genus <Emphasis Type="Italic">Teretriorhynchites</Emphasis> (Coleoptera,Rhynchitidae) from the Russian fauna

The genus Teretriorhynchites, subgenera Aphlorhynchites and Teretriorhynchites s. str., and four species (T. pubescens, T. amabilis, T. hirticollis, and T. caeruleus) from the Russian fauna are redescribed. Keys to the subgenera, species, and subspecies are given. The data on trophic associations of species of this genus are summarized.     

A review of the <Emphasis Type="Italic">Chrysolina lineella</Emphasis> species-group of the subgenus <Emphasis Type="Italic">Anopachys</Emphasis> Motschulsky, 1860, genus <Emphasis Type="Italic">Chrysolina</Emphasis> Motschulsky, 1860 (Coleoptera,Chrysomelidae, Chrysomelinae)

The Chrysolina lineella species-group of the subgenus Anopachys Motschulsky, 1860 is revised. Chrysolina watanabei Takizawa, 1970 is revalidated from the synonymy with Ch. lineigera (Jacobson, 1901). Ch. sundukovi Mikhailov, 2006 is a new junior synonym of Ch. watanabei. Special attention is paid to the infraspecific variability of the male and female genitalia. The structure of the aedeagal flagellum and the spermatheca are used as diagnostic characters. A key to species is included. Ch. watanabei is for the first time recorded from the Asian continent (Primorskii Territory of Russia and Northeastern China).     

A review of scarabs of the subgenus <Emphasis Type="Italic">Nobius</Emphasis> Mulsant et Rey,genus <Emphasis Type="Italic">Aphodius</Emphasis> Illiger (Coleoptera,Scarabaeidae), of the fauna of Russia and neighboring countries

Scarab beetles of the subgenus Nobius Mulsant et Rey, genus Aphodius Illiger, distributed in Russia and neighboring countries are reviewed. A key to the species and notes on their biology are given. The three new synonymies are established: A. serotinus (Panz.),1799 = A. x-signum Reitter, 1892, syn. n.; A. gresseri Sem. 1898 = A. korgaldzhensis Nikolajev, 1987, syn. n.; A. chaldaeus Petr., 1971 = A. moreleti Baraud, 1980, syn. n. Lectotypes of A. inclusus Reitt., 1892 and A. gresseri are designated.     

Species of the subgenus <Emphasis Type="Italic">Baudia</Emphasis> of the genus <Emphasis Type="Italic">Badister</Emphasis> (Coleoptera,Carabidae) from the southern Sikhote-Alin Mountains

Data on two species of the subgenus Baudia Ragusa, 1884, B. ishigakiensis Habu, 1975 and B. marginellus Bates, 1873 new to the fauna of the southern Sikhote-Alin Mountains, are presented. A key to species of this subgenus is provided. Holotypes of B. nigriceps A. Morawitz, 1863 and B. ussuriensis Jedli?ka, 1937 are designated. New data on the distribution of the species in Eastern Asia are given.     

A review of the <Emphasis Type="Italic">Thinodromus lunatus</Emphasis> species-group (Coleoptera,Staphylinidae)

The Thinodromus lunatus species group is revised. The following new species are described: Thinodromus (s. str.) cattiensis sp. n. from Vietnam, Thinodromus (s. str.) forsteri sp. n. from southern Thailand, Thinodromus (s. str.) himalayensis sp. n. from Nepal and northern India, Thinodromus (s. str.) inconspicuus sp. n. from southern China, Thailand, and Vietnam, and Thinodromus (s. str.) spotus sp. n. from southern China. The following new synonymy is established: Thinodromus (s. str.) deceptor (Sharp, 1889) = Thinodromus (s. str.) gravelyi (Bernhauer, 1926), syn. n.; = Thinodromus (s. str.) reitterianus (Bernhauer, 1938), syn. n. Lectotypes are designated for Trogophloeus lunatus Motschulsky, 1857, Trogophloeus pustulatus Bernhauer, 1904, Trogophloeus socius Bernhauer, 1904, Trogophloeus sumatrensis Bernhauer, 1915, Trogophloeus lewisi Cameron, 1919, Trogophloeus gravelyi Bernhauer, 1926, Trogophloeus reitterianus Bernhauer, 1938, and Trogophloeus unipustulatus Cameron, 1941. A key is presented to all the species of the Thinodromus lunatus group.     

New combinations and typifications in <Emphasis Type="Italic">Bistorta</Emphasis>, <Emphasis Type="Italic">Persicaria</Emphasis>, <Emphasis Type="Italic">Polygonum,</Emphasis> and <Emphasis Type="Italic">Rumex</Emphasis> (Polygonaceae)

New combinations are proposed in anticipation of the Polygonaceae treatment in the forthcoming volume of Intermountain Flora: Polygonum kelloggii var. esotericum, P. kelloggii var. watsonii , Rumex densiflorus var. pycnanthus , R. salicifolius var. utahensis, and R. occidentalis var. tomentellus. Typifications are proposed to facilitate ongoing studies in Polygonaceae and to maintain current usage.     

A review of the <Emphasis Type="Italic">merkli</Emphasis> group of the weevil genus <Emphasis Type="Italic">Plinthus</Emphasis> (Coleoptera,Curculionidae)

The merkli group of the weevil genus Plinthus is revised. Plinthus navarsati Davidian et Savitsky, sp. n. is described from Northeastern Turkey. New data on the morphology and geographical distribution of P. merkli Frivaldszki, 1894, P. cavazzutii Meregalli, 1985, and P. latipennis Meregalli, 1985 are given, with a key to all the four species of the merkli group.     

A new species of the weevil genus <Emphasis Type="Italic">Otiorhynchus</Emphasis> germ., subgenus <Emphasis Type="Italic">Dibredus</Emphasis> Rtt. (Coleoptera,Curculionidae: Entiminae), from Southeastern Turkey

Otiorhynchus schuberti sp. n. (subgenus Dibredus Reitter, 1912) is described from Kahramanmara? Province in Southeastern Turkey. It is closely related to O. nudiformis Reitter, 1914 and, less closely, to O. rufimanus Hochhuth, 1847, but differs from both in a small bidentate tooth on the fore femur.     

A review of the genera <Emphasis Type="Italic">Calotelea,Calliscelio</Emphasis>, and <Emphasis Type="Italic">Oxyscelio</Emphasis> (Scelioninae,Scelionidae, Proctotrupoidea) from the Palaearctic fauna

Nine new species of scelionids collected in Japan, Israel, and the Ukraine, Calotelea shimurai Kononova et Fursov, C. japonica Kononova, C. stellae Kononova, Calliscelio recens Kononova, C. floridum Kononova, C. parilis Kononova, C. ordo Kononova, Oxyscelio florum Kononova, and O. perpensum Kononova, are described. A brief morphological characteristics of the mentioned genera and some data on the geographical distribution of these species are given. Calotelea shimurai differs from C. striola Kononova in the sculpture of the metasoma (tergites I–III striate, whereas in C. striola striation present only on tergites I and II), fore-wing venation (stigmal vein of C. shimurai 0.43 times as long as postmarginal vein and 1.75 times as long as marginal one; in C. striola, stigmal vein 0.52 times as long as postmarginal vein and 1.3 times as long as marginal one), and the length of the metasoma (in C. shimurai and C. striola, metasoma 4.0 and 2.3 times as long as wide, respectively). Calotelea shimurai parasitizes in eggs of the dragonflies Aeshna nigroflava Martin, Planaeschna milnei Selys, and Boyeria macachlani (Aeshnidae, Odonata). C. japonica is closely related to C. originalis Kozlov and Kononova, but differs from it in the sculpture of the metasoma (metasomal tergites with longitudinal wrinkles against the bright smooth background; in C. originalis, tergites I and II with longitudinal wrinkles against the alveolate background), in the coloration of fore wing (infuscate in C. japonica and dark, with dark transverse stripes in C. originalis). C. stellae differs from C. artus Kozlov and Kononova in the more flattened mesoscutum (C. artus with protruding mesoscutum) and the sculpture of the metasomal tergites (in C. stellae, only petiolus and tergite II striate, while in C. artus, such striation present on tergites I–IV). C. stellae was reared from eggs of unidentified Orthoptera. C. recens is closely related to C. parilis Kononova. It can be distinguished by the fore-wing venation (C. recens has stigmal vein, which is twice as long as marginal vein and 0.66 times as long as postmarginal one; stigmal vein of C. parilis is 3 times as long as marginal vein and 0.83 times as long as postmarginal one), by the sculpture of the metasoma, and coloration of the coxae (yellow in C. recens and black in C. parilis). C. floridum is similar to C. mediterranea Kieffer, but can be identified by the length of the postmarginal vein, which is 3 times as long as the stigmal vein, whereas C. mediterranea has the postmarginal vein, which is only twice as long as the stigmal one. C. floridum also differs in the sculpture of the metasoma (C. floridum has all the metasomal tergites with longitudinal lines, while C. mediterranea has only metasomal petiolus with the same sculpture and tergites II–IV with alveolate sculpture, tergites V and VI are slightly stippled) and in the coloration of the legs, which are yellow (as coxae), while C. mediterranea has brownish black legs. C. parilis resembles C. recens, but differs from it in the fore-wing venation, sculpture of the metasoma, and coloration of the coxae. C. ordo differs from the closely related C. ruficollis Kozlov et Kononova in the head sculpture, which is finely alveolate in C. ordo and finely granulate in C. ruficollis. Oxyscelio florum is closely related to O. perpensum, but differs from it in the coloration of the body and size of the antennal segments, stigmal and postmarginal veins, and metasomal tergites. O. perpensum is closely related to O. florum. The main distinguishing morphological characters are similar to those in O. florum. O. perpensum was reared from eggs of unidentified Orthoptera.     

Molecular analysis of the genus <Emphasis Type="Italic">Anoxybacillus</Emphasis> based on sequence similarity of the genes <Emphasis Type="Italic">recN</Emphasis>, <Emphasis Type="Italic">flaA</Emphasis>, and <Emphasis Type="Italic">ftsY</Emphasis>

Genome predictions based on selected genes would be a very welcome approach for taxonomic studies. We analyzed three genes, recN, flaA, and ftsY, for determining if these genes are useful tools for systematic analyses in the genus Anoxybacillus. The genes encoding a DNA repair and genetic recombination protein (recN), the flagellin protein (flaA), and GTPase signal docking protein (ftsY) were sequenced for ten Anoxybacillus species. The sequence comparisons revealed that recN sequence similarities range between 61% and 99% in the genus Anoxybacillus. Comparisons to other bacterial recN genes indicated that levels of similarity did not differ from the levels within genus Anoxybacillus. These data showed that recN is not a useful marker for the genus Anoxybacillus. A 550–600-bp region of the flagellin gene was amplified for all Anoxybacillus strains except for Anoxybacillus contaminans. The sequence similarity of flaA gene varies between 61% and 76%. Comparisons to other bacterial flagellin genes obtained from GenBank (Bacillus, Pectinatus, Proteus, and Vibrio) indicated that the levels of similarity were lower (3–42%). Based on these data, we concluded that the variability in this single gene makes it a particularly useful marker. Another housekeeping gene ftsY suggested to reflect the G+C (mol/mol) content of whole genome was analyzed for Anoxybacillus strains. A mean difference of 1.4% was observed between the G+C content of the gene ftsY and the G+C content of the whole genome. These results showed that the gene ftsY can be used to represent whole G+C content of the Anoxybacillus species.     

Bio-resolution of glycidyl (<Emphasis Type="Italic">o</Emphasis>, <Emphasis Type="Italic">m</Emphasis>, <Emphasis Type="Italic">p</Emphasis>)-methylphenyl ethers by <Emphasis Type="Italic">Bacillus megaterium</Emphasis>

A newly isolated Bacillus megaterium with epoxide hydrolase activity resolved racemic glycidyl (o, m, p)-methylphenyl ethers to give enantiopure epoxides in 84–99% enantiomeric excess and with 21–73 enantiomeric ratios. The (S)-enantiomer was obtained from rac-glycidyl (o or m)-methylphenyl ether while the (R)-epoxides was obtained from glycidyl p-methylphenyl ether. The observations are explained at the level by enzyme-substrate docking studies.     

Floral development and systematic position of <Emphasis Type="Italic">Arillastrum</Emphasis>, <Emphasis Type="Italic">Allosyncarpia</Emphasis>, <Emphasis Type="Italic">Stockwellia</Emphasis> and <Emphasis Type="Italic">Eucalyptopsis</Emphasis> (Myrtaceae)

We have investigated the floral ontogeny of Arillastrum, Allosyncarpia, Stockwellia and Eucalyptopsis (of the eucalypt group, Myrtaceae) using scanning electron microscopy and light microscopy. Several critical characters for establishing relationships between these genera and to the eucalypts have been determined. The absence of compound petaline primordia in Arillastrum, Allosyncarpia, Stockwellia and Eucalyptopsis excludes these taxa from the eucalypt clade. Post-anthesis circumscissile abscission of the hypanthium above the ovary in Stockwellia, Eucalyptopsis and Allosyncarpia is evidence that these three taxa form a monophyletic group; undifferentiated perianth parts and elongated fusiform buds are characters that unite Stockwellia and Eucalyptopsis as sister taxa. No floral characters clearly associate Arillastrum with either the eucalypt clade or the clade of Stockwellia, Eucalyptopsis and Allosyncarpia.We gratefully acknowledge Clyde Dunlop and Bob Harwood (Northern Territory Herbarium) for collecting specimens of Allosyncarpia, and Bruce Gray (Atherton) for collecting specimens of Stockwellia. The Australian National Herbarium (CANB) kindly lent herbarium specimens of Eucalyptopsis for examination. This research was supported by a University of Melbourne Research Development Grant to Andrew Drinnan.     

New and little known species of the capsid-bug genus <Emphasis Type="Italic">Phytocoris</Emphasis>, subgenus <Emphasis Type="Italic">Soosocapsus</Emphasis> (Heteroptera: Miridae,Mirinae) from Mongolia

Three new species of the genus Phytocoris, subgenus Soosocapsus, Phytocoris kalidii sp. n., Ph. reaumuriae sp. n., and Ph. kozlovi sp. n., are described from Mongolia. Two species, Phytocoris nitrariae Xu et Zheng, 1997 and Ph. jorgitooi Kerzhner et Schuh, 1995, are recorded from Mongolia for the first time.     

A new methanol assimilating yeast, <Emphasis Type="Italic">Ogataea</Emphasis><Emphasis Type="Italic">parapolymorpha</Emphasis>, the ascosporic state of <Emphasis Type="Italic">Candida</Emphasis><Emphasis Type="Italic">parapolymorpha</Emphasis>

Ogataea parapolymorpha sp. n. (NRRL YB-1982, CBS 12304, type strain), the ascosporic state of Candida parapolymorpha, is described. The species appears homothallic, assimilates methanol as is typical of most Ogataea species and forms hat-shaped ascospores in asci that become deliquescent. O. parapolymorpha is closely related to Ogataea angusta and Ogataea polymorpha. The three species can be resolved from gene sequence analyses but are unresolved from fermentation and growth reactions that are typically used for yeast identification. On the basis of multiple isolates, O. angusta is known only from California, USA, in association with Drosophila and Aulacigaster flies, O. parapolymorpha is predominantly associated with insect frass from trees in the eastern USA but O. polymorpha has been isolated from various substrates in the USA, Brazil, Spain and Costa Rica.