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ABSTRACT The songs of the following species are presented: Conocephalus (Xiphidion) cinereus Thunberg, 1815, C. (X.) ictus (Scudder, 1875), C. (X.) magdalenae Nascrecki, 2000, C. (Anisoptera) strictus (Scudder, 1875), Dichopetala brevihastata Morse, 1902, D. castanea Rehn & Hebard, 1914, D. pollicifera Rehn & Hebard, 1914, Phyllophyllia guttulata Ståi, 1863, Stilpnochlora azteca (Saussure, 1859), Boopedon gracile Rehn, 1904, Syrbula montezuma (Saussure, 1861) and Teniopoda tamaulipensis Rehn, 1904. Considerations on distribution, taxonomy, ethology, biodiversity and conservation are given. 相似文献
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W. R. DOLLING 《Systematic Entomology》1977,2(1):27-44
Abstract. Thirteen species of the genus Vilga Stål are recognized and described or redescribed and a key for their identification is given. Lectotypes are designated for Centrocoris westwoodi Kolenati, Vilga dissimilis Distant, Vilga spinosula Montandon, Vilga mexicana Distant, Vilga penningtoni Bergroth and Vilga dallasi Distant. The new combination Vilga chilensis (Stein) is established for Arenocoris chilensis Stein. The new synonymy Vilga dissimilis Distant (= Vilga spinosula Montandon) is established. The new species Vilga brasiliensis (from Brazil), V.grisea (Brazil), V.grisescens (Brazil), V.obliqua (Brazil), V.peruviana (Peru) and V.sanctipauli (Brazil) are described. The genus Vilga is divided into six subgenera, the five new subgeneric names being Vilgula (type-species: Vilga dissimilis Distant), Trichovilga (type-species: Vilga mexicana Distant), Platyvilga (type-species: Arenocoris chilensis Stein), Laevivilga (type-species: Vilga divaricata Distant) and Echinovilga (type-species: Vilga dallasi Distant). 相似文献
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Francisco Firpo Lacoste Luis Fernández Cristina Scioscia 《Journal of fish biology》2021,99(4):1507-1512
The taxonomy of the South American genus Exomegas Gill 1883 has been unstable owing to the unknown status of the type specimen of its type species, Petromyzon macrostomus Burmeister 1868. Here the authors announce the finding of the holotype in the Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” ichthyology collection. Whereas Exomegas type species is recognized based on its holotype, Exomegas gallegensis (Smitt 1901) new status is proposed. These preliminary results resolve a century-long taxonomic uncertainty and foster a nomenclatural arrangement for a Southern Hemisphere lamprey genus. 相似文献
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The Neotropical praying mantis tribe Vatini Stål is revised using total evidence phylogenetic analysis based on molecular and coded morphological data. The subfamily Vatinae is redefined to only include Neotropical taxa with the removal of distantly related African and Asian lineages. A new tribe is erected under Vatinae (Heterovatini trib.n. ) for two unique genera with historically unstable taxonomic placement (Heterovates Saussure and Chopardiella Giglio‐Tos). Phylogenetic results and morphology support the synonymy of three genera (Lobovates Deeleman‐Reinhold, Phyllovates Kirby, and Hagiotata Saussure & Zehntner) and the validity of Chopardiella Giglio‐Tos, Heterovates Saussure, Callivates Roy, Pseudovates Saussure, Vates Burmeister, and Zoolea Audinet Serville. A new genus (Alangularis gen.n. ) is created for a former species of Vates with unique morphology and separate phylogenetic placement. All genera are redescribed based on external morphology and the male genital complex. A key to genera for Vatinae is provided with dorsal habitus images of representatives for each genus. A distinct pattern of correlated evolution of morphological characters linked to crypsis was uncovered. Cuticular leg lobes within single leg segments are evolving as sets, and serially homologous lobes appear simultaneously or in close succession. The posteroventral lobes in the apical position on thoracic femora appear to be the precursors to multiple positive rate shifts in the evolutionary accumulation of cryptic features. One shift occurred early in the evolution of Vatinae while the second occurred much later, after the loss and re‐evolution of the posteroventral lobes in the apical position on thoracic femora, a violation of Dollo's law. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:724C16AF-069A-46A1-B66C-007D8DE18C68 . 相似文献
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George Poinar Jr. 《Historical Biology》2013,25(2-3):223-226
A walking stick, Clonistria dominicana n. sp. (Phasmatodea: Diapheromeridae: Diapheromerinae: Diapheromerini) is described from Dominican amber. The new species can be distinguished from extant members of the genus by the long hind leg tarsomere II (over six times the length of the foreleg tarsomere II), the short metanotum, which is only half the length of the median segment and the prominent median carina. Two phasmatid eggs in separate pieces of Dominican amber are also presented. One of these has characteristics of the genus Clonistria Stål, 1875, which supports the generic placement of C. dominicana. The second egg resembles those of the genus Malacomorpha Rehn, 1906 (Pseudophasmatidae: Pseudophasmatinae). Both of these genera occur in Hispaniola today. 相似文献
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A report of Mantodea species collected in South-East Vietnam (provinces Dong Nai, Binh Phuoc and Lam Dong) is presented. New for Vietnam are the subfamily Phyllothelyinae, the tribe Anaxarchini of the subfamily Hymenopodinae and the species Leptomantella lactea (Saussure, 1870), Tropidomantis gressitti Tinkham, 1937, Amantis bolivari Giglio-Tos, 1915, Anaxarcha graminea Stål, 1877, Creobroter nebulosa Zheng, 1988, Phyllothelys breve (Wang, 1993), Ceratocrania macra Westwood, 1889, Ceratomantis saussuri Wood-Mason, 1876 and Theopompa tosta Stål, 1877, as well as five additional species whose precise identifications are less certain. Eighteen species are new for the South-East region and seven are new for the provinces sampled. The fauna of Vietnam now contains 69 species of Mantodea, 40 of which occur in the South-East region. Morphological, taxonomical and identification details for selected species are discussed and illustrated. 相似文献
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Jesús María Pérez-Jiménez María Desamparados Soler-Cruz Isidoro Ruiz-Martínez Manuel Díaz-López Jose Enrique Granados-Torres 《Systematic parasitology》1992,22(3):215-219
After studying some material belonging to genus Aegypoecus Clay & Meinertzhagen, 1939 captured on the head and neck of a European black vulture Aegypius monachus, the authors have identified these specimens as Aegypoecus brevicollis (Burmeister, 1838). Morphobiometric data on adults (both males and females) are given, and the designation of a neotype for this species is proposed. 相似文献
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我国三种蝼蛄的雄性生殖器鉴别 总被引:3,自引:0,他引:3
本文记述 3种蝼蛄 (单刺蝼蛄GryllotalpaunispinaSaussure,东方蝼蛄G .orientalisBurmeister及河南蝼蛄G .henanaCaietNiu)的雄生殖器 相似文献
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Land M Lapidus A Mayilraj S Chen F Copeland A Del Rio TG Nolan M Lucas S Tice H Cheng JF Chertkov O Bruce D Goodwin L Pitluck S Rohde M Göker M Pati A Ivanova N Mavromatis K Chen A Palaniappan K Hauser L Chang YJ Jeffries CC Brettin T Detter JC Han C Chain P Tindall BJ Bristow J Eisen JA Markowitz V Hugenholtz P Kyrpides NC Klenk HP 《Standards in genomic sciences》2009,1(1):46-53
Actinosynnema mirum Hasegawa et al. 1978 is the type species of the genus, and is of phylogenetic interest because of its central phylogenetic location in the Actino-synnemataceae, a rapidly growing family within the actinobacterial suborder Pseudo-nocardineae. A. mirum is characterized by its motile spores borne on synnemata and as a producer of nocardicin antibiotics. It is capable of growing aerobically and under a moderate CO(2) atmosphere. The strain is a Gram-positive, aerial and substrate mycelium producing bacterium, originally isolated from a grass blade collected from the Raritan River, New Jersey. Here we describe the features of this organism, together with the complete genome sequence and annotation. This is the first complete genome sequence of a member of the family Actinosynnemataceae, and only the second sequence from the actinobacterial suborder Pseudonocardineae. The 8,248,144 bp long single replicon genome with its 7100 protein-coding and 77 RNA genes is part of the Genomic Encyclopedia of Bacteria and Archaea project. 相似文献
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Tice H Mayilraj S Sims D Lapidus A Nolan M Lucas S Glavina Del Rio T Copeland A Cheng JF Meincke L Bruce D Goodwin L Pitluck S Ivanova N Mavromatis K Ovchinnikova G Pati A Chen A Palaniappan K Land M Hauser L Chang YJ Jeffries CD Detter JC Brettin T Rohde M Göker M Bristow J Eisen JA Markowitz V Hugenholtz P Kyrpides NC Klenk HP Chen F 《Standards in genomic sciences》2010,2(2):168-175
Nakamurella multipartita (Yoshimi et al. 1996) Tao et al. 2004 is the type species of the monospecific genus Nakamurella in the actinobacterial suborder Frankineae. The nonmotile, coccus-shaped strain was isolated from activated sludge acclimated with sugar-containing synthetic wastewater, and is capable of accumulating large amounts of polysaccharides in its cells. Here we describe the features of the organism, together with the complete genome sequence and annotation. This is the first complete genome sequence of a member of the family Nakamurellaceae. The 6,060,298 bp long single replicon genome with its 5415 protein-coding and 56 RNA genes is part of the Genomic Encyclopedia of Bacteria and Archaea project. 相似文献
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Similascarophis (Cystidicolidae) n. gen. is proposed. In the mouth of specimens of this genus, submedial labia are absent and pseudolabia do not have any part projecting toward the central oral opening. These nematodes were obtained from the alimentary tract of 7 marine fish species along the coast of Chile: Bovichthys chilensis Regan, Eleginops maclovinus (Cuvier), Pinguipes chilensis (Valenciennes), Cilus gilberti (Abbott), Cheilodactylus variegatus Valenciennes, Girella laevifrons (Tschudi), and Graus nigra Philippi. Morphology and morphometry are compared between 2 new Similascarophis species: Similascarophis maulensis n. sp. and S. chilensis n. sp., which differ in the presence of sublabia and in the length of the glandular esophagus and left spicule. We also recorded Similascarophis sp. in 2 other host species, which showed some distinct proportional measurements, although these differences were not sufficiently clear to identify them as a new species. 相似文献
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The North American (north of Mexico) species of the tenebrionid genus Paratenetus Spinola are reviewed and a key is presented for their identification. Five species are recognized, P. gibbipennis Motschulsky, P. fuscus LeConte, P. punctatus Spinola and two sp. n., P. exutus [type locality: Tabusintac, Nova Scotia] and P. texanus [type locality: Port Isabel, Cameron County, Texas]. Two syn. n. are proposed: P. cribratus Motschulsky, 1868 with P. gibbipennis Motschulsky, 1868 and P. crinitus Fall, 1907 with P. fuscus LeConte, 1850. A lectotype is selected for Paratenetus punctatus Spinola. A type species is designated for Storthephora Mäklin, 1875 (Storthephora denticollis Mäklin, 1875). 相似文献
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Lapidus A Pukall R Labuttii K Copeland A Del Rio TG Nolan M Chen F Lucas S Tice H Cheng JF Bruce D Goodwin L Pitluck S Rohde M Göker M Pati A Ivanova N Mavrommatis K Chen A Palaniappan K D'haeseleer P Chain P Bristow J Eisen JA Markowitz V Hugenholtz P Kyrpides NC Klenk HP 《Standards in genomic sciences》2009,1(1):3-11
Brachybacterium faecium Collins et al. 1988 is the type species of the genus, and is of phylogenetic interest because of its location in the Dermabacteraceae, a rather isolated family within the actinobacterial suborder Micrococcineae. B. faecium is known for its rod-coccus growth cycle and the ability to degrade uric acid. It grows aerobically or weakly anaerobically. The strain described in this report is a free-living, nonmotile, Gram-positive bacterium, originally isolated from poultry deep litter. Here we describe the features of this organism, together with the complete genome sequence, and annotation. This is the first complete genome sequence of a member of the actinobacterial family Dermabacteraceae, and the 3,614,992 bp long single replicon genome with its 3129 protein-coding and 69 RNA genes is part of the Genomic Encyclopedia of Bacteria and Archaea project. 相似文献
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The external morphology and anatomy of the opisthobranch gastropodsMiamira
sinuata (van Hasselt, 1824) and Orodoris miamiranaBergh, 1875, the type
species of the genera Miamira Bergh, 1875and Orodoris Bergh, 1875, and
their phylogenetic relationshipsare studied. The phylogeny obtained supports the placement ofM. sinuata and O. miamirana in the genus Ceratosoma J. E. Gray,
1850.Therefore, Miamira and Orodoris become synonyms of the seniorvalid
name Ceratosoma. In addition, the family name MiamiridaeBergh, 1891, based on Miamira, is newly recognized as a synonymof Chromodorididae Bergh, 1891. Ceratosoma sinuata and C. miamirana are more closely relatedto the
highly derived Ceratosoma alleni than to other membersof the genus. C. miamirana appears to present reversal to theplesiomorphic state in the body shape and has secondarily
lostits mantle glands. (Received 5 January 1998; accepted 23 April 1998) 相似文献
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Pukall R Lapidus A Nolan M Copeland A Glavina Del Rio T Lucas S Chen F Tice H Cheng JF Chertkov O Bruce D Goodwin L Kuske C Brettin T Detter JC Han C Pitluck S Pati A Mavrommatis K Ivanova N Ovchinnikova G Chen A Palaniappan K Schneider S Rohde M Chain P D'haeseleer P Göker M Bristow J Eisen JA Markowitz V Kyrpides NC Klenk HP Hugenholtz P 《Standards in genomic sciences》2009,1(3):234-241
Stackebrandtia nassauensis Labeda and Kroppenstedt (2005) is the type species of the genus Stackebrandtia, and a member of the actinobacterial family Glycomycetaceae. Stackebrandtia currently contains two species, which are differentiated from Glycomyces spp. by cellular fatty acid and menaquinone composition. Strain LLR-40K-21(T) is Gram-positive, aerobic, and nonmotile, with a branched substrate mycelium and on some media an aerial mycelium. The strain was originally isolated from a soil sample collected from a road side in Nassau, Bahamas. Here we describe the features of this organism, together with the complete genome sequence and annotation. This is the first complete genome sequence of the actinobacterial suborder Glycomycineae. The 6,841,557 bp long single replicon genome with its 6487 protein-coding and 53 RNA genes is part of the Genomic Encyclopedia of Bacteria and Archaea project. 相似文献
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The type status is described of 404 taxa classified within the family Bulimulidae (superfamily Orthalicoidea) and kept in the London museum. Lectotypes are designated for Bulimus aurifluus Pfeiffer, 1857; Otostomus bartletti H. Adams, 1867; Helix cactorum d’Orbigny, 1835; Bulimus caliginosus Reeve, 1849; Bulimus chemnitzioides Forbes, 1850; Bulimus cinereus Reeve, 1849; Helix cora d’Orbigny, 1835; Bulimus fallax Pfeiffer, 1853; Bulimus felix Pfeiffer, 1862; Bulimus fontainii d’Orbigny, 1838; Bulimus fourmiersi d’Orbigny, 1837; Bulimus (Mesembrinus) gealei H. Adams, 1867; Bulimus gruneri Pfeiffer, 1846; Bulimus humboldtii Reeve, 1849; Helix hygrohylaea d’Orbigny, 1835; Bulimus jussieui Pfeiffer, 1846; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895; Helix lichnorum d’Orbigny, 1835; Bulimulus (Drymaeus) lucidus da Costa, 1898; Bulimus luridus Pfeiffer, 1863; Bulimus meleagris Pfeiffer, 1853; Bulimus monachus Pfeiffer, 1857; Bulimus montagnei d’Orbigny, 1837; Helix montivaga d’Orbigny, 1835; Bulimus muliebris Reeve, 1849; Bulimus nigrofasciatus Pfeiffer in Philippi 1846; Bulimus nitelinus Reeve, 1849; Helix oreades d’Orbigny, 1835; Helix polymorpha d’Orbigny, 1835; Bulimus praetextus Reeve, 1849; Bulinus proteus Broderip, 1832; Bulimus rusticellus Morelet, 1860; Helix sporadica d’Orbigny, 1835; Bulimus sulphureus Pfeiffer, 1857; Helix thamnoica var. marmorata d’Orbigny, 1835; Bulinus translucens Broderip in Broderip and Sowerby I 1832; Helix trichoda d’Orbigny, 1835; Bulinus ustulatus Sowerby I, 1833; Bulimus voithianus Pfeiffer, 1847; Bulimus yungasensis d’Orbigny, 1837.The type status of the following taxa is changed to lectotype in accordance with Art. 74.6 ICZN: Bulimulus (Drymaeus) caucaensis da Costa, 1898; Drymaeus exoticus da Costa, 1901; Bulimulus (Drymaeus) hidalgoi da Costa, 1898; Bulimulus (Drymaeus) interruptus Preston, 1909; Bulimulus (Drymaeus) inusitatus Fulton, 1900; Bulimulus latecolumellaris Preston, 1909; Bulimus (Otostomus) napo Angas, 1878; Drymaeus notabilis da Costa, 1906; Drymaeus notatus da Costa, 1906; Bulimulus (Drymaeus) nubilus Preston, 1903; Drymaeus obliquistriatus da Costa, 1901; Bulimus (Drymaeus) ochrocheilus E.A. Smith, 1877; Bulimus (Drymaeus) orthostoma E.A. Smith, 1877; Drymaeus expansus perenensis da Costa, 1901; Bulimulus pergracilis Rolle, 1904; Bulimulus (Drymaeus) plicatoliratus da Costa, 1898; Drymaeus prestoni da Costa, 1906; Drymaeus punctatus da Costa, 1907; Bulimus (Leptomerus) sanctaeluciae E.A. Smith, 1889; Bulimulus (Drymaeus) selli Preston, 1909; Drymaeus subventricosus da Costa, 1901; Bulimulus (Drymaeus) tigrinus da Costa, 1898; Drymaeus volsus Fulton, 1907; Drymaeus wintlei Finch, 1929; Bulimus zhorquinensis Angas, 1879; Bulimulus (Drymaeus) ziczac da Costa, 1898.The following junior subjective synonyms are established: Bulimus antioquensis Pfeiffer, 1855 = Bulimus baranguillanus Pfeiffer, 1853; Drymaeus bellus da Costa, 1906 = Drymaeus blandi Pilsbry, 1897; Bulimus hachensis Reeve 1850 = Bulimus gruneri Pfeiffer, 1846 = Bulimus columbianus Lea, 1838; Bulimus (Otostomus) lamas Higgins 1868 = Bulimus trujillensis Philippi, 1867; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895 = Bulimulus (Drymaeus) binominis E.A. Smith, 1895; Drymaeus multispira da Costa, 1904 = Helix torallyi d’Orbigny, 1835; Bulimulus (Drymaeus) plicatoliratus Da Costa, 1898 = Bulimus convexus Pfeiffer, 1855; Bulimus sugillatus Pfeiffer, 1857 = Bulimus rivasii d’Orbigny, 1837; Bulimus meridionalis Reeve 1848 [June] = Bulimus voithianus Pfeiffer, 1847.New combinations are: Bostryx montagnei (d’Orbigny, 1837); Bostryx obliquiportus (da Costa, 1901); Bulimulus heloicus (d’Orbigny, 1835); Drymaeus (Drymaeus) lusorius (Pfeiffer, 1855); Drymaeus (Drymaeus) trigonostomus (Jonas, 1844); Drymaeus (Drymaeus) wintlei Finch, 1929; Drymaeus (Mesembrinus) conicus da Costa, 1907; Kuschelenia (Kuschelenia) culminea culminea (d’Orbigny, 1835); Kuschelenia (Kuschelenia) culmineus edwardsi (Morelet, 1863); Kuschelenia (K.) gayi (Pfeiffer, 1857); Kuschelenia (Kuschelenia) tupacii (d’Orbigny, 1835); Kuschelenia (Vermiculatus) anthisanensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) aquilus (Reeve, 1848); Kuschelenia (Vermiculatus) bicolor (Sowerby I, 1835); Kuschelenia (Vermiculatus) caliginosus (Reeve, 1849); Kuschelenia (Vermiculatus) cotopaxiensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) filaris (Pfeiffer, 1853); Kuschelenia (Vermiculatus) ochracea (Morelet, 1863); Kuschelenia (Vermiculatus) petiti (Pfeiffer, 1846); Kuschelenia (Vermiculatus) purpuratus (Reeve, 1849); Kuschelenia (Vermiculatus) quechuarum (Crawford, 1939); Naesiotus cinereus (Reeve, 1849); Naesiotus dentritis (Morelet, 1863); Naesiotus fontainii (d’Orbigny, 1838); Naesiotus orbignyi (Pfeiffer, 1846); Protoglyptus pilosus (Guppy, 1871); Protoglyptus sanctaeluciae (E.A. Smith, 1889).Type material of the following taxa is figured herein for the first time: Bulimus cinereus Reeve, 1849; Bulimus coriaceus Pfeiffer, 1857; Bulimulus laxostylus Rolle, 1904; Bulimus pliculatus Pfeiffer, 1857; Bulimus simpliculus Pfeiffer, 1855. 相似文献