TAXONOMIC REVISION OF NEARCTIC, MEXICAN, AND WEST INDIAN OODINI (COLEOPTERA: CARABIDAE)

1996 ◽  
Vol 128 (3) ◽  
pp. 443-537 ◽  
Author(s):  
Yves Bousquet

AbstractEight genera and 25 species are recognized among the Nearctic, Mexican, and West Indian Oodini. Four new species are described: Oodinus pseudopiceus (type locality: Hillsborough River St. Pk., Hillsborough Co., Florida); Oodinus similis (type locality: San Quintín, Chiapas, Mexico); Oodinus darlingtoni (type locality: Cauto El Cristo, Oriente, Cuba); and Oodinus edentulus (type locality: 31.8 mi E Francisco Escárcega, Campeche, Mexico). Oodes fluvialis LeConte, 1863, previously recognized as a subspecies of O. americanus Dejean, 1826, is given specific status. The following new synonymies are established: Eulachnocrepis Habu, 1956 with Lachnocrepis LeConte, 1853; Stenocrepis texana (LeConte, 1863), S. chalcas Bates, 1882, and S. chalcochrous Chaudoir, 1883 with S. insulana (Jacquelin du Val, 1857); Stenocrepis quatuordecimstriata (Chaudoir, 1843), S. picipes (LeConte, 1844), S. stenocephala (LaFerté-Sénectère, 1851), and S. sulcata Chevrolat, 1863 with S. mexicana (Chevrolat, 1835). Lectotypes are designated for Oodinus alutaceus (Bates, 1882), Oodes amaroides Dejean, 1831, O. fluvialis LeConte, 1863, O. americanus Dejean, 1826, Stenocrepis texana (LeConte, 1863), S. chalcas Bates, 1882, S. lecontei (Chaudoir, 1857), S. quatuordecimstriata (Chaudoir, 1843), S. picipes (LeConte, 1844), S. cuprea (Chaudoir, 1843), S. tibialis (Chevrolat, 1834), S. femoralis (Chaudoir, 1835), S. elegans (LeConte, 1851), and S. gratiosa (Bates, 1882). The genus-group name Nanodes Habu, 1956, a homonym of Nanodes Schönherr, 1825, is replaced by Nanodiodes, new replacement name. For each genus treated, the following are provided: citation of original description and selected references, notes about synonymy (if required), description, geographical distribution and diversity, and monophyly and phylogenetic relationships. For each species included, the following are given: citation of original description and synonymies, type material, etymology (for new species only), notes about synonymy (if required), diagnosis, description, geographical distribution, bionomics, and phylogenetic relationships (if the genus includes more than two species). Keys to genera and, for each genus, to species are included. The species distributions are mapped, and the important structural features are illustrated.

Zootaxa ◽  
2017 ◽  
Vol 4269 (2) ◽  
pp. 197 ◽  
Author(s):  
CHRISTER HANSSON ◽  
PAOLO NAVONE

The European species of Diglyphus Walker are reviewed. Fifteen species are included. One of these, D. clematidis sp. n., is described as new, and one, D. anadolucus Doganlar, is recorded as new to Europe. Several of the species have their geographical distribution increased as many new country records are introduced. New host records and compilation of host records from the literature are presented in tables. To facilitate the identification of the species a key and numerous illustrations are included. The identity of one of the species described from Europe, D. phytomyzae Ruschka, is unclear. It has not been possible to locate the type material of this species and the original description is not detailed enough to make an unambiguous interpretation possible. Two species, D. scapus Yefremova from Iran and D. sensilis Yefremova from Turkey, are discussed as they occur in the vicinity of Europe.


1994 ◽  
Vol 126 (4) ◽  
pp. 1007-1059 ◽  
Author(s):  
Bradley J. Sinclair

AbstractThere are 16 species of Trichoclinocera Collin recognized from the Nearctic region, including eight new species. Four of six species-groups of Trichoclinocera are recognized in the Nearctic region, with the following included species: (1) T. comata group — T. cascadensis sp.nov. (type-locality Starvation Creek, Oregon, U.S.A.), T. comata (Melander) comb.nov., and T. rupestris sp.nov. (type-locality Newton Creek, Wyoming, U.S.A.); (2) T. dolicheretma group — T. dolicheretma (Melander); (3) T. lapponica group — T. lapponica (Ringdahl) comb.nov.; (4) T. longipes group — T. agilis sp.nov. (type-locality Fall Creek Falls, Tennessee, U.S.A.), T. ctenistes (Melander), T. dasycoxa sp.nov. (type-locality Ottawa, Ontario, Canada), T. falcata sp.nov. (type-locality Gatineau Park, Quebec, Canada), T. fumosa (Vaillant) comb.nov., T. hamifera (Melander), T. longipes (Walker). T. minor (Melander), T. ozarkensis sp.nov. (type-locality Haw Creek Falls, Arkansas, U.S.A.), and T. pectinifemur sp.nov. (type-locality Phoenixville, Pennsylvania, U.S.A.). The following new synonyms are proposed: T. brunnipennis (Melander) = T. dolicheretma; and Seguyella saltans (Vaillant) = T. hamifera. Lectotypes are designated for T. comata, T. ctenistes, T. dolicheretma, T. brunnipennis, T. hamifera, T. lapponica, and T. stackelbergi Collin. Seguyella Vaillant and Acanthoclinocera Saigusa are newly synonymized with Trichoclinocera and all species formerly placed in these genera are transferred to Trichoclinocera, except Acanthoclinocera glaucescens (Brunetti) which is transferred as Wiedemannia glaucescens (Brunetti) comb.nov.This revision includes a key to Nearctic species, a description of each species, and maps of species distributions. Homologies of male terminalia of Clinocerinae are summarized and the first descriptions of the immature stages of species of Trichoclinocera also are provided. A world list of described species of Trichoclinocera is provided and all species are assigned to one of six species-groups, except T. cummingi sp.nov. (type-locality Robber’s Cave, Oklahoma. U.S.A.), T. fluviatilis (Brunetti) comb.nov., T. fuscipennis Saigusa, and T. maewa Smith, which remain unplaced. The monophyly of Trichoclinocera is justified and phylogenetic relationships to the remaining Clinocerinae and among species-groups are discussed.


2015 ◽  
Vol 42 (2) ◽  
pp. 226-235 ◽  
Author(s):  
G. N. H. Waller

Eight species of mesoplodont whales (genus Mesoplodon Gervais, 1850) named during the nineteenth century are based on valid descriptions. A checklist with the original description and type material for each of these species is provided. Additional data given may include type locality and illustrative sources, type material holding institution and type registration number(s). The only type specimen for which a record of external morphology was published relates to the 1803 stranding of Sowerby's beaked whale (Mesoplodon bidens).


Zootaxa ◽  
2012 ◽  
Vol 3373 (1) ◽  
pp. 1 ◽  
Author(s):  
HOUHUN LI ◽  
KLAUS SATTLER

The genus Mesophleps Hübner (Lepidoptera: Gelechiidae) is revised; 54 available names (including one unjustifiedemendation), one junior primary homonym and one unavailable name were considered; type material of 44 previouslydescribed nominal species was examined. Nine new species are described: M. acutunca sp. nov., M. bifidella sp. nov., M.unguella sp. nov., M. gigantella sp. nov., M. coffeae sp. nov., M. parvella sp. nov., M. aspina sp. nov., M. truncatella sp.nov. and M. undulatella sp. nov. Two possibly new species are discussed but not formally named for lack of material.Twenty-five new combinations are introduced: M. safranella (Legrand, 1965) comb. nov., M. epichorda (Turner, 1919)comb. nov., M. tabellata (Meyrick, 1913) comb. nov., M. crocina (Meyrick, 1904) comb. nov., M. ochracella (Turati,1926) comb. nov., M. geodes (Meyrick, 1929) comb. nov., M. catericta (Meyrick, 1927) comb. nov., M. tephrastis(Meyrick, 1904) comb. nov., M. cycnobathra (Lower, 1898) comb. nov., M. tetrachroa (Lower, 1898) comb. nov., M.ochroloma (Lower, 1901) comb. nov., M. trichombra (Lower, 1898) comb. nov., M. mylicotis (Meyrick, 1904) comb. nov.,M. macrosemus (Lower, 1900) comb. nov., M. apentheta (Turner, 1919) comb. nov., M. meliphanes (Lower, 1894) comb.nov., M. chloranthes (Lower, 1900) comb. nov., M. centrothetis (Meyrick, 1904) comb. nov., M. chloristis (Meyrick,1904) comb. nov., M. argonota (Lower, 1901) comb. nov., Megacraspedus arnaldi (Turati & Krüger, 1936) comb. nov.,Aponoea cinerellus (Turati, 1930) comb. nov., Pycnobathra acromelas (Turner, 1919) comb. nov., Sarotorna mesoleuca(Lower, 1900) comb. nov., S. dentata Meyrick, 1904, comb. nov. One species, Nothris mesophracta Turner, 1919, isremoved from Mesophleps but no current genus is available. Fourteen new synonymies (one genus, 13 species-group taxa)are established: Bucolarcha Meyrick, 1929, syn. nov. of Mesophleps Hübner, [1825]; Stiphrostola longinqua Meyrick,1923, syn. nov. and Brachyacma trychota Meyrick, 1929, syn. nov. of M. ioloncha (Meyrick, 1905); Lipatia crotalariellaBusck, 1910, syn. nov. of M. adustipennis (Walsingham, 1897); Brachyacma epichorda Turner, 1919, syn. nov. of M.epiochra (Meyrick, 1886); Mesophleps pudicellus var. apicellus Caradja, 1920, syn. nov. and Mesophleps silacellus subsp.calaritanus Amsel, 1939, syn. nov. of M. silacella (Hübner, 1796); Mesophleps lala Agenjo, [1961], syn. nov. of M.corsicella (Herrich-Schäffer, 1856); Crossobela barysphena Meyrick, 1923, syn. nov. of M. trinotella Herrich-Schäffer,1856; Mesophleps orientella Nel & Nel, 2003, syn. n. and Mesophleps gallicella Varenne & Nel, 2011, syn. nov. of M.ochracella (Turati, 1926); Nothris centrothetis Meyrick, 1904, syn. nov. and Nothris chloristis Meyrick, 1904, syn. nov.of M. chloranthes (Lower, 1900); Mesophleps cinerellus Turati, 1930, syn. nov. of Aponoea obtusipalpis Walsingham,1905. One genus and one species are recalled from synonymy: Pycnobathra Lower, 1901, gen. rev., and M. ioloncha(Meyrick, 1905) sp. rev. Lectotypes are designated, in accordance with the Code, article 74.7.3, for 14 species: Gelechiapalpigera Walsingham, 1891; Paraspistes ioloncha Meyrick, 1905; Lathontogenus adustipennis Walsingham, 1897;Brachyacma epichorda Turner, 1919; Nothris crocina Meyrick, 1904; Nothris ochracella Turati, 1926; Nothris tephrastisMeyrick, 1904; Ypsolophus ochroloma Lower, 1901; Ypsolophus macrosemus Lower, 1900; Nothris centrothetis Meyrick,1904; Nothris chloristis Meyrick, 1904; Ypsolophus argonota Lower, 1901; Mesophleps arnaldi Turati & Krüger, 1936,and Mesophleps cinerellus Turati, 1930. Mesophleps is a widely distributed Old World genus, except for one New Worldspecies, with seed-feeding larvae on Cupressaceae, Cistaceae, Cruciferae (Brassicaceae), Leguminosae (Fabaceae), Rubiaceae and doubtfully Dipterocarpaceae.


Zootaxa ◽  
2018 ◽  
Vol 4531 (4) ◽  
pp. 451
Author(s):  
DIEGO AGUILAR FACHIN ◽  
MARTIN HAUSER

The Neotropical genus Himantigera James in James & McFadden, 1982, is revised. Two new species are described and illustrated—H. amauroptera nov. sp. (Costa Rica, Panama, Colombia), and H. xanthopoda nov. sp. (Mexico, Nicaragua, Costa Rica). Three species are transferred from Himantigera to Sargus Fabricius, 1798—S. dichrous (Schiner, 1868) comb. nov., S. flavoniger Lindner, 1928 comb. rev. and S. fulvithorax (Bigot, 1879) comb. nov. One species is transferred to Microchrysa Loew, 1855—M. splendens (Schiner, 1868) comb. nov. Himantigera jamesi Lindner, 1969 syn. nov. is proposed as a junior synonym of H. superba Lindner, 1949. The type species H. silvestris McFadden, 1982, as well as H. nigrifemorata Macquart, 1847 and H. superba Lindner, are herein redescribed and illustrated. Photographs of the type specimens of these three species are provided. Two unnamed species of Himantigera (sp. A and sp. B) are also described given that they have slight differences, but because we had only one specimen of each species, we did not officially describe them. This updates the total number of extant Himantigera from eight sensu Woodley (2001) to seven species. The species Merosargus apicalis Lindner, 1935, although never referred to the genus Himantigera or Himantoloba McFadden 1970, is also transferred to the genus Sargus. A key to all species of Himantigera and a map expanding geographical distribution of the genus are also presented, with the first records of the genus for Nicaragua, Colombia, Venezuela, Trinidad and Tobago, Ecuador and Bolivia. 


1987 ◽  
Vol 119 (3) ◽  
pp. 215-230 ◽  
Author(s):  
Alasdair J. Ritchie ◽  
Joseph D. Shorthouse

AbstractThe species of Synophromorpha Ashmead (Hymenoptera: Cynipidae) are reviewed. One new species is described (Synophromorpha kaulbarsi; type locality: Naupan, Puebla, Mexico). The previously described species (S. rubi Weld, S. sylvestris (O.S.), and S. terricola Weld) are redescribed, and a key to species is presented. All species are illustrated for the first time. Synophromorpha sylvestris is designated type-species for the genus and a lectotype is chosen. Hypotheses on the phylogenetic relationships between the species of Synophromorpha are presented.


Zootaxa ◽  
2018 ◽  
Vol 4449 (1) ◽  
pp. 1 ◽  
Author(s):  
MARIANA CHANI-POSSE ◽  
ALFRED F. NEWTON ◽  
ASLAK KAPPEL HANSEN ◽  
ALEXEY SOLODOVNIKOV

A checklist of all described species of Philonthina, a subtribe of the staphylinid tribe Staphylinini, known to occur in Central and South America (CASA) is presented. Included for each species, and for synonyms known from CASA, is a reference to the original description, type locality and type depository, and for each species the known distribution within and outside CASA. Type material was sought in the main European and American collections where it is deposited (BMNH, MNHUB, IRSNB and FMNH) and is summarized for all indigenous CASA species, with lectotypes designated for 16 names and confirmation of holotypes and prior designation of lectotypes when necessary. Based on recent phylogenetic work in Philonthina and our revision of types of CASA species of Philonthus Stephens, 1829 and Belonuchus Nordmann, 1837, some taxonomic changes are proposed. Thirty-one species of Philonthus are transferred to Belonuchus (16), Gabrius Stephens 1829 (14), and Bisnius Stephens 1829 (one) resulting in the following new combinations: B. abnormalis (Sharp 1885), B. celatus (Sharp 1885), B. corticalis (Sharp 1885), B. extremus (Sharp 1885), B. infimus (Sharp 1885), B. iteratus (Sharp 1887), B. latecinctus (Sharp 1885), B. lucilius (Sharp 1885), B. muticus (Sharp 1876), B. optatus (Sharp 1885), B. platypterus (Sharp 1885), B. rufiventris (Sharp 1887), B. rufocaudus (Sharp 1885), B. rufopygus (Sharp 1885), B. serraticornis (Sharp 1876), B. supernus (Herman 2001), G. approximans (Sharp 1885), G. armatipes (Sharp 1885), G. atricolor (Sharp 1885), G. championi (Sharp 1885), G. dampfi (Bernhauer 1929), G. elegans (Sharp 1885), G. forsterianus (Scheerpeltz 1960), G. misellus (Sharp 1885), G. nugax (Sharp 1885), G. ovaticeps (Sharp 1885), G. peruvianus (Bernhauer 1916), G. planulatus (Sharp 1885), G. rusticus (Sharp 1885), G. serpens (Sharp 1885) and Bi. subaeneipennis (Bernhauer 1916). Endeius nitidipennis Solier 1849 is transferred to Gabrius, resulting in the following new combination, G. nitidipennis (Solier 1849). Leptopeltus carchiensis Chani-Posse & Asenjo 2013 is proposed as junior synonym of Philonthus divisus Sharp 1891, which is transferred to Leptopeltus Bernhauer 1906 resulting in a new combination: Leptopeltus divisus (Sharp 1891). Belonuchus penetrans Silvestri 1946 is transferred to Pridonius Blackwelder 1952 as a new combination. Lectotypes are designated for Atopocentrum mirabile Bernhauer 1906, Philonthus armatipes Sharp 1885, Ph. atricolor Sharp 1885, Ph. championi Sharp 1885, Ph. misellus Sharp 1885, Ph. planulatus Sharp 1885, Ph. rusticus Sharp 1885, Ph. serpens Sharp 1885, Ph. abnormalis Sharp 1885, Ph. celatus Sharp 1885, Ph. infimus Sharp 1885, Ph. latecinctus Sharp 1885, Ph. muticus Sharp 1876, Ph. platypterus Sharp 1885, Ph. rufocaudus Sharp 1885 and Ph. rufopygus Sharp 1885. Of the 543 currently known species of Philonthina reported from CASA, at least 14 are believed to be adventive from elsewhere, 56 may occur naturally elsewhere, and 473 (87%) are evidently endemic to this region. Of the 31 genera represented by these described species, 20 (65%) are endemic to CASA. One genus, Gabronthus Tottenham 1955, is adventive. However, the actual philonthine fauna of CASA will undoubtedly be much larger, and the generic composition highly modified, when the fauna is fully explored and studied within a phylogenetical framework. 


2020 ◽  
pp. 41-48
Author(s):  
FELIX SCHLAGINTWEIT

Orbitolina daviesi Hofker, 1966 (family Orbitolinidae) was validly described and thoroughly illustrated from Thanetian limestones of Pakistan. Although its attribution to the genus Orbitolina d’Orbigny and any phylogenetic relationships with the Cretaceous taxa have been refuted shortly afterwards, the species has not been taxonomically revised since then. Karsella hottingeri Sirel, 1999 was established as new genus and new species from the Thanetian of Turkey, without taking into account J. Hofker’s publication. The original description and genus diagnosis of Karsella has meanwhile been emended to include the occurrence of a radial zone with septula that follow a zig-zag pattern and associated linear arrangement of the foramina, as well as a complex embryo. Orbitolina daviesi clearly displays these features and is here considered a species of the genus Karsella Sirel. Karsella hottingeri is regarded as a subjective junior synonym of O. daviesi Hofker and therefore, the only species of the genus is given as a new combination: Karsella daviesi (Hofker). From a suprageneric viewpoint, the two Paleogene genera Karsella Sirel and Cushmania Silvestri display a complex embryo and might belong to a new subfamily of the Orbitolinidae, phylogenetically different and unrelated to the lower-mid Cretaceous Orbitolininae.


Crustaceana ◽  
2018 ◽  
Vol 91 (6) ◽  
pp. 677-731
Author(s):  
Yenumula Ranga Reddy

Abstract Only eight groundwater crustacean species were known in India till the end of 20th century. Analysis of about 4000 samples collected during 2000-2016 from diverse groundwater habitats, especially in certain pockets of the deltaic belt of the Rivers Krishna and Godavari in the southeastern peninsular India, has so far yielded about 90 new crustacean taxa. Of these, 67 new species have been described formally, which include, respectively, 34, 27, 3, 2 and 1 species each of Copepoda, Bathynellacea, Amphipoda, Isopoda and Ostracoda. The updated checklist presented herein includes a total of 87 species in 45 genera, 22 families and 8 orders. For each species, the reference to its original description, type locality, distribution, and ecological notes, co-occurring fauna, if any, and sampling method(s) are given. Besides map-pointing the type localities of the species, brief notes are given on the biogeography and conservation.


Zootaxa ◽  
2005 ◽  
Vol 1066 (1) ◽  
pp. 1 ◽  
Author(s):  
FRANZ-RUDOLF SCHNITZLER ◽  
QIAO WANG

The genus Zorion Pascoe (Cerambycidae: Cerambycinae), commonly known as flower longhorn beetle, is endemic to New Zealand where it is widely distributed on the main and some offshore islands. A taxonomic revision of Zorion adults is given, including a description and illustrations of the genus. The previously known species Z. batesi Sharp, Z. guttigerum (Westwood), Z. minutum (Fabricius), and Z. opacum Sharp are redescribed; Z. castum Broun is synonymised with Z.guttigerum. Lectotypes are designated here for Z. guttigerum and Z. opacum. Six new species are described, Z. angustifasciatum sp. nov. from Three Kings Islands, Z. australe sp. nov. from South Island, Z. dugdalei sp. nov. from Poor Knights Island, Z. kaikouraiensis sp. nov. from the Kaikoura region, Z. nonmaculatum sp. nov. from D’Urville Islands, and Z. taranakiensis sp. nov. from the Taranaki region. The species Z. exiguum Gmelin has been excluded from the study because neither the original description nor the holotype could be located. A key to all ten species is included and diagnostic elytral spot patterns are illustrated. Biological information presented is based on publications, collecting records and our observations. A distribution map for all species is included and species distribution is discussed in relation to New Zealand’s biogeographical history.


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