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1.
The genus Gasteruption Latreille, 1796 (Hymenoptera: Evanioidea: Gasteruptiidae: Gasteruptiinae) from North Iran and Turkey is revised, keyed and fully illustrated for the first time. In total 36 species are treated of which 33 are recorded from Turkey and 23 from Iran. Fifteen species are new for science: Gasteruption
aciculatum van Achterberg, sp. n., Gasteruption
agrenum van Achterberg, sp. n., Gasteruption
brevibasale van Achterberg & Saure, sp. n., Gasteruption
coriacoxale van Achterberg, sp. n., Gasteruption
flavimarginatum van Achterberg, sp. n., Gasteruption
heminitidum van Achterberg, sp. n., Gasteruption
henseni van Achterberg, sp. n., Gasteruption
ischnolaimum van Achterberg, sp. n., Gasteruption
nigrapiculatum van Achterberg, sp. n., Gasteruption
paglianoi van Achterberg & Saure, sp. n., Gasteruption
pseudolaticeps van Achterberg, sp. n., Gasteruption
punctifrons van Achterberg, sp. n., Gasteruption
schmideggeri van Achterberg & Saure, sp. n., Gasteruption
scorteum van Achterberg, sp. n. and Gasteruption
smitorum van Achterberg, sp. n. Twenty-one species are reported new for Turkey and 16 species new for Iran. Fifteen new synonyms are proposed: Foenus
terrestris Tournier, 1877, Gasteruption
trifossulatum Kieffer, 1904, and Gasteruption
ignoratum Kieffer, 1912, of Gasteruption
caucasicum (Guérin-Méneville, 1844); Gasteruption
daisyi Alekseev, 1993, of Gasteruption
dolichoderum Schletterer, 1889; Gasteruption
assectator
var.
nitidulum Schletterer, 1885, of Gasteruption
freyi (Tournier, 1877); Gasteruption
schossmannae Madl, 1987, of Gasteruption
hastator (Fabricius, 1804); Gasteryption
fallaciosum Semenov, 1892, Gasteruption
dubiosum Semenov, 1892 and Gasteruption
obsoletum Semenov, 1892, of Gasteruption
insidiosum Semenov, 1892; Gasteryption
schewyrewi Semenov, 1892, of Gasteruption
jaculator (Linnaeus, 1758); Gasteruption
floreum Szépligeti, 1903, of Gasteruption
lugubre Schletterer, 1889; Gasteruption
trichotomma Kieffer, 1904, and Gasteruption
palaestinum Pic, 1916, of Gasteruption
merceti Kieffer, 1904; Gasteryption
foveiceps Semenov, 1892, of Gasteruption
nigrescens Schletterer, 1885, and Gasteruption
libanense Pic, 1916, of Gasteruption
syriacum Szépligeti, 1903. Gasteruption
lugubre Schletterer, 1889, is recognised as a valid species. Lectotypes are designated for Ichneumon
assectator Linnaeus, 1758; Ichneumon
jaculator Linnaeus, 1758; Foenus
terrestris Tournier, 1877; Foenus
freyi Tournier, 1877; Foenus
nigripes Tournier, 1877; Foenus
goberti Tournier, 1877; Foenus
granulithorax Tournier, 1877; Foenus
minutus Tournier, 1877; Foenus
borealis Thomson, 1883; Faenus
diversipes Abeille de Perrin, 1879; Foenus
rugulosus Abeille de Perrin, 1879; Faenus
obliteratus Abeille de Perrin, 1879; Faenus
undulatum Abeille de Perrin, 1879; Faenus
variolosus Abeille de Perrin, 1879; Gasteruption
distinguendum Schletterer, 1885; Gasteruption
laeviceps Schletterer, 1885; Gasteruption
thomsonii Schletterer, 1885; Gasteruption
foveolatum Schletterer, 1889; Gasteruption
sowae Schletterer, 1901; Gasteruption
foveolum Szépligeti, 1903; Gasteruption
floreum Szépligeti, 1903; Gasteruption
caudatum Szépligeti, 1903; Gasteruption
syriacum Szépligeti, 1903; Gasteruption
merceti Kieffer, 1904 and Gasteruption
ignoratum Kieffer, 1912. A neotype is designated for Gasteruption
tournieri Schletterer, 1885. 相似文献
2.
This systematic study documents the taxonomy, diversity, and distribution of the tarantula spider genus Aphonopelma Pocock, 1901 within the United States. By employing phylogenomic, morphological, and geospatial data, we evaluated all 55 nominal species in the United States to examine the evolutionary history of Aphonopelma and the group’s taxonomy by implementing an integrative approach to species delimitation. Based on our analyses, we now recognize only 29 distinct species in the United States. We propose 33 new synonymies (Aphonopelma
apacheum, Aphonopelma
minchi, Aphonopelma
rothi, Aphonopelma
schmidti, Aphonopelma
stahnkei = Aphonopelma
chalcodes; Aphonopelma
arnoldi = Aphonopelma
armada; Aphonopelma
behlei, Aphonopelma
vogelae = Aphonopelma
marxi; Aphonopelma
breenei = Aphonopelma
anax; Aphonopelma
chambersi, Aphonopelma
clarum, Aphonopelma
cryptethum, Aphonopelma
sandersoni, Aphonopelma
sullivani = Aphonopelma
eutylenum; Aphonopelma
clarki, Aphonopelma
coloradanum, Aphonopelma
echinum, Aphonopelma
gurleyi, Aphonopelma
harlingenum, Aphonopelma
odelli, Aphonopelma
waconum, Aphonopelma
wichitanum = Aphonopelma
hentzi; Aphonopelma
heterops = Aphonopelma
moderatum; Aphonopelma
jungi, Aphonopelma
punzoi = Aphonopelma
vorhiesi; Aphonopelma
brunnius, Aphonopelma
chamberlini, Aphonopelma
iviei, Aphonopelma
lithodomum, Aphonopelma
smithi, Aphonopelma
zionis = Aphonopelma
iodius; Aphonopelma
phanum, Aphonopelma
reversum = Aphonopelma
steindachneri), 14 new species (Aphonopelma
atomicum
sp. n., Aphonopelma
catalina
sp. n., Aphonopelma
chiricahua
sp. n., Aphonopelma
icenoglei
sp. n., Aphonopelma
johnnycashi
sp. n., Aphonopelma
madera
sp. n., Aphonopelma
mareki
sp. n., Aphonopelma
moellendorfi
sp. n., Aphonopelma
parvum
sp. n., Aphonopelma
peloncillo
sp. n., Aphonopelma
prenticei
sp. n., Aphonopelma
saguaro
sp. n., Aphonopelma
superstitionense
sp. n., and Aphonopelma
xwalxwal
sp. n.), and seven nomina dubia (Aphonopelma
baergi, Aphonopelma
cratium, Aphonopelma
hollyi, Aphonopelma
mordax, Aphonopelma
radinum, Aphonopelma
rusticum, Aphonopelma
texense). Our proposed species tree based on Anchored Enrichment data delimits five major lineages: a monotypic group confined to California, a western group, an eastern group, a group primarily distributed in high-elevation areas, and a group that comprises several miniaturized species. Multiple species are distributed throughout two biodiversity hotspots in the United States (i.e., California Floristic Province and Madrean Pine-Oak Woodlands). Keys are provided for identification of both males and females. By conducting the most comprehensive sampling of a single theraphosid genus to date, this research significantly broadens the scope of prior molecular and morphological investigations, finally bringing a modern understanding of species delimitation in this dynamic and charismatic group of spiders. 相似文献
3.
Kipling Will 《ZooKeys》2015,(545):131-137
Taxonomic changes are made for several problematic Australian Carabidae in the tribes Harpalini, Abacetini, Pterostichini, and Oodini. Examination of types resulted in the synonymy of Veradia Castelnau, 1867 with Leconomerus Chaudoir, 1850; Nelidus Chaudoir, 1878, Feronista Moore, 1965, and Australomasoreus Baehr, 2007 with Cerabilia Castelnau, 1867; and newly combining Fouquetius
variabilis Straneo, 1960 in the genus Pediomorphus Chaudoir, 1878; Australomasoreus
monteithi Baehr, 2007 in the genus Cerabilia Castelnau, 1867; and Anatrichis
lilliputana W.J. Macleay, 1888 in the genus Nanodiodes Bousquet, 1996. Cuneipectus Sloane, 1907 is placed in Pterostichini Bonelli, 1810, which is a senior synonym of Cuneipectini Sloane, 1907. 相似文献
4.
Bruno Massa 《ZooKeys》2015,(524):17-44
Results of the study of specimens collected in tropical Africa and preserved in different European collections and museums are reported and extensively illustrated. The following three new species are described: Horatosphaga
aethiopica
sp. n., Dapanera
occulta
sp. n. and Cestromoecha
laeglae
sp. n. In addition, new diagnostic characters or distributional data for Ruspolia
differens (Serville, 1838), Thyridorhoptrum
senegalense Krauss, 1877, Horatosphaga
leggei (Kirby, 1909), Horatosphaga
linearis (Rehn, 1910), Preussia
lobatipes Karsch, 1890 and Dapanera
eidmanni Ebner, 1943 are reported. Finally, Symmetropleura
plana (Walker, 1869) is proposed to be transferred to the genus Symmetrokarschia Massa, 2015, Conocephalus
carbonarius (Redtenbacher, 1891) to the genus Thyridorhoptrum Rehn & Hebard, 1915; the genus Gonatoxia Karsch, 1889 is proposed to be synonymized with Dapanera Karsch, 1889. 相似文献
5.
Six new species of Lycocerus Gorham are described, Lycocerus
gracilicornis
sp. n. (China: Sichuan), Lycocerus
longihirtus
sp. n. (China: Yunnan), Lycocerus
sichuanus
sp. n. (China: Sichuan), Lycocerus
hubeiensis
sp. n. (China: Hubei), Lycocerus
napolovi
sp. n. (Vietnam: Sa Pa) and Lycocerus
quadrilineatus
sp. n. (Vietnam: Sa Pa), and provided with illustrations of habitus, antennae and aedeagi of male or and antennae, abdominal sternites VIII and genitalia of female. Lycocerus
rubroniger Švihla, 2011 is synonymized with Lycocerus
obscurus Pic, 1916. Lycocerus
hickeri Pic, 1934 and Lycocerus
obscurus are provided with illustrations of abdominal sternites VIII of female. Nine species are recorded from China for the first time, Lycocerus
bicoloripennis (Pic, 1924), Lycocerus
caliginostus Gorham, 1889, Lycocerus
jendeki Švihla, 2005, Lycocerus
malaisei (Wittmer, 1995), Lycocerus
obscurus, Lycocerus
olivaceus (Wittmer, 1995), Lycocerus
purpureus Kazantsev, 2007, Lycocerus
ruficornis (Wittmer, 1995) and Lycocerus
semiextensus (Wittmer, 1995), and Lycocerus
ruficornis is also recorded for Myanmar for the first time. 相似文献
6.
7.
Hume Douglas Patrice Bouchard Robert S. Anderson Pierre de Tonnancour Robert Vigneault Reginald P. Webster 《ZooKeys》2013,(309):13-48
The following species of Curculionoidea are recorded from Canada for the first time, in ten cases also representing new records at the generic level: Ischnopterapion (Ischnopterapion) loti (Kirby, 1808); Stenopterapion meliloti (Kirby, 1808) (both Brentidae); Atrichonotus taeniatulus (Berg, 1881); Barinus cribricollis (LeConte, 1876); Caulophilus dubius (Horn, 1873); Cionus scrophulariae (Linnaeus, 1758); Cryptorhynchus tristis LeConte, 1876; Cylindrocopturus furnissi Buchanan, 1940; Cylindrocopturus quercus (Say, 1832); Desmoglyptus crenatus (LeConte, 1876); Pnigodes setosus LeConte, 1876; Pseudopentarthrum parvicollis (Casey, 1892); Sibariops confinis (LeConte, 1876); Sibariops confusus (Boheman, 1836); Smicronyx griseus LeConte, 1876; Smicronyx lineolatus Casey, 1892; Euwallacea validus (Eichhoff, 1875); Hylocurus rudis (LeConte, 1876); Lymantor alaskanus Wood, 1978; Phloeotribus scabricollis (Hopkins, 1916); Scolytus oregoni Blackman, 1934; Xyleborus celsus Eichhoff, 1868; Xyleborus ferrugineus (Fabricius, 1801); Xylosandrus crassiusculus (Motschulsky, 1866) (all Curculionidae). In addition the following species were recorded for the first time from these provinces and territories: Yukon – Dendroctonus simplex LeConte, 1868; Phloetribus piceae Swaine, 1911 (both Curculionidae); Northwest Territories – Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Nunavut – Dendroctonus simplex LeConte, 1868 (Curculionidae); Alberta – Anthonomus tectus LeConte, 1876; Promecotarsus densus Casey, 1892; Dendroctonus ponderosae Hopkins, 1902; Hylastes macer LeConte, 1868; Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Saskatchewan – Phloeotribus liminaris (Harris, 1852); Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Manitoba – Cosmobaris scolopacea Germar, 1819; Listronotus maculicollis (Kirby, 1837); Listronotus punctiger LeConte, 1876; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Tyloderma foveolatum (Say, 1832); (all Curculionidae); Ontario – Trichapion nigrum (Herbst, 1797); Nanophyes marmoratus marmoratus (Goeze, 1777) (both Brentidae); Asperosoma echinatum (Fall, 1917); Micracis suturalis LeConte, 1868; Orchestes alni (Linnaeus, 1758); Phloeosinus pini Swaine, 1915; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Quebec – Trigonorhinus alternatus (Say, 1826); Trigonorhinus tomentosus tomentosus (Say, 1826) (both Anthribidae); Trichapion nigrum (Herbst, 1797); Trichapion porcatum (Boheman, 1839); Nanophyes marmoratus marmoratus (Goeze, 1777) (all Brentidae); Lissorhoptrus oryzophilus Kuschel, 1952 (Brachyceridae); Acalles carinatus LeConte, 1876; Ampeloglypter ampelopsis (Riley, 1869); Anthonomus rufipes LeConte, 1876; Anthonomus suturalis LeConte, 1824; Ceutorhynchus hamiltoni Dietz, 1896; Curculio pardalis (Chittenden, 1908); Cyrtepistomus castaneus (Roelofs, 1873); Larinus planus (Fabricius, 1792); Mecinus janthinus (Germar, 1821); Microhyus setiger LeConte, 1876; Microplontus campestris (Gyllenhal, 1837); Orchestes alni (Linnaeus, 1758); Otiorhynchus ligustici (Linnaeus, 1758); Rhinusa neta (Germar, 1821); Trichobaris trinotata (Say, 1832); Tychius liljebladi Blatchley, 1916; Xyleborinus attenuatus (Blandford, 1894); Xyleborus affinis Eichhoff, 1868 (all Curculionidae); Sphenophorus incongruus Chittenden, 1905 (Dryophthoridae); New Brunswick – Euparius paganus Gyllenhal, 1833; Allandrus populi Pierce, 1930; Gonotropis dorsalis (Thunberg, 1796); Euxenus punctatus LeConte, 1876 (all Anthribidae); Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Pseudanthonomus seriesetosus Dietz, 1891; Curculio sulcatulus (Casey, 1897); Lignyodes bischoffi (Blatchley, 1916); Lignyodes horridulus (Casey, 1892); Dietzella zimmermanni (Gyllenhal, 1837); Parenthis vestitus Dietz, 1896; Pelenomus squamosus LeConte, 1876; Psomus armatus Dietz, 1891; Rhyncolus macrops Buchanan, 1946; Magdalis inconspicua Horn, 1873; Magdalis salicis Horn, 1873 (all Curculionidae); Nova Scotia – Dryocoetes autographus (Ratzeburg, 1837); Ips perroti Swaine, 1915; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Prince Edward Island – Dryocoetes caryi Hopkins, 1915 (Curculionidae); Newfoundland – Scolytus piceae (Swaine, 1910) (Curculionidae).Published records of Dendroctonus simplex LeConte, 1868 from Northwest Territories should be reassigned to Nunavut, leaving no documented record for NWT. Collection data are provided for eight provincial and national records published without further information previously. 相似文献
8.
Japanese melithaeid type material is re-examined and re-described. The sclerites of the different species are depicted using Scanning Electron Microscopy. All Japanese species of the family Melithaeidae treated here belong to the genus Melithaea and are endemic to Japanese waters. Old museum material and newly collected specimens from Japanese waters are identified after comparison with this type material. Acabaria
modesta
var.
abyssicola is regarded a separate species, here named Melithaea
abyssicola (Kükenthal, 1909). In addition, 11 new species are described: Melithaea
boninensis
sp. n., Melithaea
doederleini
sp. n., Melithaea
isonoi
sp. n., Melithaea
keramaensis
sp. n., Melithaea
oyeni
sp. n., Melithaea
ryukyukensis
sp. n., Melithaea
sagamiensis
sp. n., Melithaea
satsumaensis
sp. n., Melithaea
suensoni
sp. n., Melithaea
tanseii
sp. n., and Melithaea
tokaraensis
sp. n.. Pleurocorallium
confusum Moroff, 1902, Pleurocoralloides
formosum Moroff, 1902, Melitodes
flabellifera Kükenthal, 1908, and Melitodes
densa Kükenthal, 1908 are synonymized with Melithaea
japonica (Verrill, 1865). We have designated a neotype for Melithaea
mutsu Minobe, 1929. A key to the Japanese melithaeids is presented. 相似文献
9.
Barna Páll-Gergely Prem B. Budha Fred Naggs Thierry Backeljau Takahiro Asami 《ZooKeys》2015,(529):1-70
All known taxa of the genus Endothyrella Zilch, 1960 (family Plectopylidae) are reviewed. Altogether 23 Endothyrella species are recognized. All species are illustrated and whenever possible, photographs of the available type specimens are provided. Five new species are described: Endothyrella
angulata Budha & Páll-Gergely, sp. n., Endothyrella
dolakhaensis Budha & Páll-Gergely, sp. n. and Endothyrella
nepalica Budha & Páll-Gergely, sp. n. from Nepal, Endothyrella
robustistriata Páll-Gergely, sp. n. from the Naga Hills, India, and Endothyrella
inexpectata Páll-Gergely, sp. n. from Sichuan, China. Helix (Plectopylis) munipurensis Godwin-Austen, 1875 is synonymized with Helix (Plectopylis) serica Godwin-Austen, 1875, and Plectopylis (Endothyra) gregorsoni Gude, 1915 is synonymized with Helix (Plectopylis) macromphalus W. Blanford, 1870. Plectopylis
plectostoma
var.
exerta Gude, 1901 is a synonym of Plectopylis
plectostoma
var.
tricarinata Gude, 1896, which is a species in its own right. Five species of the genus Chersaecia viz. Plectopylis (Chersaecia) bedfordi Gude, 1915, Helix (Plectopylis) brahma Godwin-Austen, 1879, Helix (Plectopylis) Oglei Godwin-Austen, 1879, Helix (Plectopylis) serica Godwin-Austen, 1875, and Plectopylis (Endothyra) williamsoni Gude, 1915 are moved to Endothyrella. The holotype of Plectopylis
hanleyi Godwin-Austen, 1879 seems to be lost; therefore, Plectopylis
hanleyi is considered to be a nomen dubium. 相似文献
10.
A critical and annotated catalogue of 183 types of Hymenoptera
Chrysididae belonging to 124 taxa housed in the Radoszkowski collection is given. Radoszkowski type material from other institutes has also been checked. Six lectotypes are designated in Kraków (ISEA-PAN): Chrysis
acceptabilis Radoszkowski, 1891; Chrysis
persica Radoczkowsky, 1881; Chrysis
daphnis Mocsáry, 1889; Chrysis
lagodechii Radoszkowski, 1889; Chrysis
remota Mocsáry, 1889 and Chrysis
vagans Radoszkowski, 1877. The lectotype of Brugmoia
pellucida Radoszkowski, 1877 is designated in Moscow (MMU). Four new combinations are proposed: Philoctetes
araraticus (Radoszkowski, 1890), comb. n.; Pseudomalus
hypocrita (du Buysson, 1893), comb. n.; Chrysis
eldari (Radoszkowski, 1893), comb. n.; and Chrysura
mlokosewitzi (Radoszkowski, 1889), comb. n.. Ten new synonyms are given: Chrysis
auropunctata Mocsáry, 1889, syn. n. of Chrysis
angolensis Radoszkovsky, 1881; Chrysis
chrysochlora Mocsáry, 1889, syn. n. and Chrysis
viridans Radoszkowski, 1891, syn. n. of Chrysis
keriensis Radoszkowski, 1887; Chrysis
angustifrons
var.
ignicollis Trautmann, 1926, syn. n. of Chrysis
eldari (Radoszkowski, 1893); Chrysis
maracandensis
var.
simulatrix Radoszkowski, 1891, syn. n. of Chrysis
maracandensis Radoszkowski, 1877; Chrysis
pulchra Radoszkovsky, 1880, syn. n. of Spinolia
dallatorreana (Mocsáry, 1896); Chrysis
rubricollis du Buysson, 1900, syn. n. of Chrysis
eldari (Radoszkowski, 1893); Chrysis
subcoerulea Radoszkowski, 1891, syn. n. of Chrysis
chlorochrysa Mocsáry, 1889; Chrysis
therates Mocsáry, 1889, syn. n. of Chrysis
principalis Smith, 1874; and Notozus
komarowi Radoszkowski, 1893, syn. n. of Elampus
obesus (Mocsáry, 1890). One species is revaluated: Chrysis
chalcochrysa Mocsáry, 1887. Chrysis
kizilkumiana Rosa is the new name for Chrysis
uljanini Radoszkowski & Mocsáry, 1889 nec Radoszkowski, 1877. Pictures of seventy-seven type specimens are given. 相似文献
11.
Chirasak Sutcharit Jonathan Ablett Piyoros Tongkerd Fred Naggs Somsak Panha 《ZooKeys》2015,(492):49-105
The collection of the Southeast Asian tree snail genus Amphidromus Albers, 1850 at the Natural History Museum, London includes more than 100 lots of type specimens representing 85 name-bearing types, 9 paratypes and 6 paralectotypes, and one nomen nudum. Lectotypes are here designated for Amphidromus
cambojiensis, Amphidromus
perakensis
globosus, Amphidromus
columellaris
gloriosa, Amphidromus
maculiferus
inflata, Amphidromus
lepidus, Amphidromus
sinistralis
lutea, Amphidromus
moniliferus, Amphidromus
maculiferus
obscura, Amphidromus
sinistralis
rosea and Amphidromus
sinensi
vicaria. In addition, the missing types of A.A. Gould were discovered and their type status is discussed. A complete catalogue of these types, including colour photographs is provided for the first time. After examining these type specimens, two new Amphidromus species, Amphidromus (Syndromus) globonevilli Sutcharit & Panha, sp. n. and Amphidromus (Syndromus) principalis Sutcharit & Panha, sp. n. were recognized and are described herein. 相似文献
12.
A review on the Chinese species of Tetraserica Ahrens, 2004, is presented. The lectotype of Tetraserica
tonkinensis (Moser, 1908), comb. n. is designated. Twenty-nine new Tetraserica species are described from China and adjacent regions: Tetraserica
anhuaensis
sp. n., Tetraserica
changjiangensis
sp. n., Tetraserica
changshouensis
sp. n., Tetraserica
damaidiensis
sp. n., Tetraserica
daqingshanica
sp. n., Tetraserica
fikaceki
sp. n., Tetraserica
graciliforceps
sp. n., Tetraserica
jinghongensis
sp. n., Tetraserica
leishanica
sp. n., Tetraserica
liangheensis
sp. n., Tetraserica
linaoshanica
sp. n., Tetraserica
longipenis
sp. n., Tetraserica
longzhouensis
sp. n., Tetraserica
maoershanensis
sp. n., Tetraserica
mengeana
sp. n., Tetraserica
menglongensis
sp. n., Tetraserica
pingjiangensis
sp. n., Tetraserica
ruiliana
sp. n., Tetraserica
ruiliensis
sp. n., Tetraserica
sculptilis
sp. n., Tetraserica
shangsiensis
sp. n., Tetraserica
shunbiensis
sp. n., Tetraserica
sigulianshanica
sp. n., Tetraserica
tianchiensis
sp. n., Tetraserica
wandingensis
sp. n., Tetraserica
wangtongensis
sp. n., Tetraserica
xichouensis
sp. n., Tetraserica
yaoanica
sp. n., Tetraserica
yaoquensis
sp. n. A key to the Chinese Tetraserica species is given, species distribution as well as the habitus and male genitalia of all species are illustrated. 相似文献
13.
New material collected recently throughout the Afrotropical region has led to a major reassessment of taxa within the genera Anelaphinis Kolbe, 1892, Atrichelaphinis Kraatz, 1898 and other closely related genera. As a result, the name Megalleucosma Antoine, 1989 is here synonymised with Anelaphinis and a lectotype is designated for the type species, Cetonia
dominula Harold, 1879. The genus Atrichelaphinis is redefined and a new subgenus, Atrichelaphinis (Eugeaphinis), is proposed for Elaphinis
simillima Ancey, 1883, Elaphinis
vermiculata Fairmaire, 1894, Niphetophora
rhodesiana Péringuey, 1907, Atrichelaphinis
deplanata Moser, 1907 (with Anelaphinis
kwangensis Burgeon, 1931 as junior synonym) and Anelaphinis
sternalis Moser, 1914. Additionally, three new species and one new subspecies are recognised and described in this new subgenus: Atrichelaphinis (Eugeaphinis) bomboesbergica
sp. n. from South Africa; Atrichelaphinis (Eugeaphinis) bjornstadi
sp. n. from Tanzania; Atrichelaphinis (Eugeaphinis) garnieri
sp. n. from south–east Africa (Tanzania, Zimbabwe); and Atrichelaphinis (Eugeaphinis) deplanata
minettii
ssp. n. from central Africa (Malawi, Mozambique, Congo-Kinshasa, Congo-Brazzaville, South Africa, Rwanda, Zambia, Zimbabwe). The genus Atrichelaphinis is compared to its closest relatives and two separate keys are proposed, one for Atrichelaphinis and one for the sub-Saharan genera exhibiting completely or partially fused parameres. 相似文献
14.
A new species of Anteon Jurine, 1807 is described from Thailand, Nan Province: Anteon
huettingeri
sp. n. Morphologically the new species is similar to Anteon
borneanum Olmi, 1984, Anteon
jurineanum Latreille, 1809, Anteon
insertum Olmi, 1991, Anteon
yasumatsui Olmi, 1984, Anteon
sarawaki Olmi, 1984, Anteon
thai Olmi, 1984 and Anteon
krombeini Olmi, 1984, but it is clearly different for the numerous sensorial processes present on the inner side of the paramere; these processes are absent in the other above species. Published identification keys to the Oriental species of Anteon are modified to include the new species. 相似文献
15.
The Indo-Malayan and Palearctic species of Oxyscelio (Hymenoptera: Platygastridae s.l.) are revised. A total of 90 species are recognized as valid, 19 of which are redescribed - Oxyscelio acutiventris (Kieffer), Oxyscelio brevinervis (Kieffer), Oxyscelio carinatus (Kieffer), Oxyscelio ceylonensis (Dodd), Oxyscelio consobrinus (Kieffer), Oxyscelio crassicornis (Kieffer), Oxyscelio cupularis (Kieffer), Oxyscelio dorsalis (Kieffer), Oxyscelio excavatus (Kieffer), Oxyscelio flavipennis (Kieffer), Oxyscelio florus Kononova, Oxyscelio foveatus Kieffer, Oxyscelio kiefferi Dodd, Oxyscelio magnus (Kieffer), Oxyscelio marginalis (Kieffer), Oxyscelio naraws Kozlov & Lê, Oxyscelio perpensus Kononova, Oxyscelio rugosus (Kieffer) and Oxyscelio spinosiceps (Kieffer), and 71 which are described as new - Oxyscelio aclavae Burks, sp. n., Oxyscelio amrichae Burks, sp. n., Oxyscelio anguli Burks, sp. n., Oxyscelio angustifrons Burks, sp. n., Oxyscelio angustinubbin Burks, sp. n., Oxyscelio arcus Burks, sp. n., Oxyscelio arvi Burks, sp. n., Oxyscelio asperi Burks, sp. n., Oxyscelio aureamediocritas Burks, sp. n., Oxyscelio bipunctuum Burks, sp. n., Oxyscelio brevidentis Burks, sp. n., Oxyscelio caesitas Burks, sp. n., Oxyscelio capilli Burks, sp. n., Oxyscelio capitis Burks, sp. n., Oxyscelio cavinetrion Burks, sp. n., Oxyscelio chimaerae Burks, sp. n., Oxyscelio codae Burks, sp. n., Oxyscelio convergens Burks, sp. n., Oxyscelio cordis Burks, sp. n., Oxyscelio crateris Burks, sp. n., Oxyscelio crebritas Burks, sp. n., Oxyscelio crustum Burks, sp. n., Oxyscelio cuculli Burks, sp. n., Oxyscelio cyrtomesos Burks, sp. n., Oxyscelio dasymesos Burks, sp. n., Oxyscelio dasynoton Burks, sp. n., Oxyscelio dermatoglyphes Burks, sp. n., Oxyscelio doumao Burks, sp. n., Oxyscelio fistulae Burks, sp. n., Oxyscelio flabellae Burks, sp. n., Oxyscelio flaviventris Burks, sp. n., Oxyscelio fodiens Burks, sp. n., Oxyscelio fossarum Burks, sp. n., Oxyscelio fossularum Burks, sp. n., Oxyscelio genae Burks, sp. n., Oxyscelio granorum Burks, sp. n., Oxyscelio granuli Burks, sp. n., Oxyscelio greenacus Burks, sp. n., Oxyscelio halmaherae Burks, sp. n., Oxyscelio intermedietas Burks, sp. n., Oxyscelio jaune Burks, sp. n., Oxyscelio jugi Burks, sp. n., Oxyscelio kramatos Burks, sp. n., Oxyscelio labis Burks, sp. n., Oxyscelio lacunae Burks, sp. n., Oxyscelio latinubbin Burks, sp. n., Oxyscelio latitudinis Burks, sp. n., Oxyscelio limae Burks, sp. n., Oxyscelio longiventris Burks, sp. n., Oxyscelio mesiodentis Burks, sp. n., Oxyscelio mollitia Burks, sp. n., Oxyscelio nasolabii Burks, sp. n., Oxyscelio nodorum Burks, sp. n., Oxyscelio noduli Burks, sp. n., Oxyscelio nubbin Burks, sp. n., Oxyscelio obsidiani Burks, sp. n., Oxyscelio ogive Burks, sp. n., Oxyscelio operimenti Burks, sp. n., Oxyscelio peludo Burks, sp. n., Oxyscelio planocarinae Burks, sp. n., Oxyscelio praecipitis Burks, sp. n., Oxyscelio reflectens Burks, sp. n., Oxyscelio regionis Burks, sp. n., Oxyscelio sinuum Burks, sp. n., Oxyscelio spinae Burks, sp. n., Oxyscelio striarum Burks, sp. n., Oxyscelio tecti Burks, sp. n., Oxyscelio unguis Burks, sp. n., Oxyscelio vadorum Burks, sp. n., Oxyscelio vittae Burks, sp. n. and Oxyscelio zeuctomesos. Neotypes are designated for nine species, including the type species O. foveatus Kieffer, Oxyscelio brevinervis (Kieffer), Oxyscelio bifurcatus (Kieffer), Oxyscelio frontalis (Kieffer), Oxyscelio crassicornis (Kieffer), Oxyscelio cupularis (Kieffer), Oxyscelio foveatus Kieffer, Oxyscelio kiefferi Dodd, Oxyscelio magnus (Kieffer) and Oxyscelio marginalis (Kieffer). Oxyscelio bifurcatus (Kieffer) syn. n. and Oxyscelio frontalis (Kieffer) syn. n. are synonymized under Oxyscelio consobrinus (Kieffer). The fauna is divided into 13 species groups, with six species unplaced to a group. A phylogenetic analysis employing 73 morphological characters did not find most of these groups to be monophyletic, but they are retained to aid in specimen identification. Potential biogeographical patterns are discussed, including regional variation in surface sculpture and a morphological link between Sri Lankan and Australian species. 相似文献
16.
Eugenie Phillips-Rodríguez Jerry A. Powell Winnie Hallwachs Daniel H. Janzen 《ZooKeys》2014,(461):1-86
We discuss 45 Costa Rican species of Ethmia Hübner, 1819, including 23 previously described: Ethmia
delliella (Fernald), Ethmia
bittenella (Busck), Ethmia
festiva Busck, Ethmia
scythropa Walsingham, Ethmia
perpulchra Walsingham, Ethmia
terpnota Walsingham, Ethmia
elutella Busck, Ethmia
janzeni Powell, Ethmia
ungulatella Busck, Ethmia
exornata (Zeller), Ethmia
phylacis Walsingham, Ethmia
mnesicosma Meyrick, Ethmia
chemsaki Powell, Ethmia
baliostola Walsingham, Ethmia
duckworthi Powell, Ethmia
sandra Powell, Ethmia
nigritaenia Powell, Ethmia
catapeltica Meyrick, Ethmia
lichyi Powell, Ethmia
transversella Busck, Ethmia
similatella Busck, Ethmia
hammella Busck, Ethmia
linda Busck, and 22 new species: Ethmia
blaineorum, Ethmia
millerorum, Ethmia
dianemillerae, Ethmia
adrianforsythi, Ethmia
stephenrumseyi, Ethmia
berndkerni, Ethmia
dimauraorum, Ethmia
billalleni, Ethmia
ehakernae, Ethmia
helenmillerae, Ethmia
johnpringlei, Ethmia
laphamorum, Ethmia
petersterlingi, Ethmia
lesliesaulae, Ethmia
turnerorum, Ethmia
normgershenzi, Ethmia
nicholsonorum, Ethmia
hendersonorum, Ethmia
randyjonesi, Ethmia
randycurtisi, Ethmia
miriamschulmanae and Ethmia
tilneyorum. We illustrate all species and their male and female genitalia, along with distribution maps of Costa Rican localities. Immature stages are illustrated for 11 species, and food plants are listed when known. Gesneriaceae is added as a new food plant family record for Ethmia. CO1 nucleotide sequences (“DNA barcodes”) were obtained for 41 of the species. 相似文献
17.
We carried out a quantitative assessment of the consumption of herbaceous plants by Opatrum
sabulosum (Linnaeus, 1761) – a highly significant agricultural pest species. We researched the feeding preferences of this pest species with respect to 33 uncultivated and 22 cultivated plant species. This species of darkling beetle feeds on many uncultivated plant species, including those with hairy leaves and bitter milky sap, such as Scabiosa
ucrainca (5.21 mg/specimen/24 hours), Euphorbia
virgata (3.45), Solanum
nigrum (3.32), Centauria
scabiosa (2.47), Lamium
album (2.41), Aristolochia
clematitis (1.76), Chenopodium
album (1.73), Arctium
lappa (1.51), Asperula
odorata (1.20). A high rate of leaf consumption is also characteristic for cultivated species, for example, Perilla
nankinensis (5.05 mg/specimen/24 hours), Lycopersicon
esculentum (3.75), Tropaeolum
majus (3.29), Nicotiana
tabacum (2.66), Rumex
acetosa (1.96), Beta
vulgaris (1.27). Opatrum
sabulosum is capable of feeding on plants which are poisonous to cattle. This species of darkling beetle consumes 95.5% of the cultivated and 48.5% of the uncultivated herbaceous plants researched. 相似文献
18.
A taxonomic review of Korean Gyrinidae is presented. Seven species [Dineutus
orientalis (Modeer, 1776), Gyrinus
gestroi Régimbart, 1883, Gyrinus
japonicus Sharp, 1873, Gyrinus
pullatus Zaitzev, 1908, Orectochilus
punctipennis Sharp, 1884, Orectochilus
Regimbarti Sharp, 1884 and Orectochilus
villosus (Müller, 1776)] in three genera are recognized, one of which (Orectochilus
punctipennis Sharp, 1884) is reported for the first time in Korea. We also found that Gyrinus
curtus Motschulsky, 1866 previously recorded in Korea was an incorrect identification of Gyrinus
pullatus Zaitzev, 1908. Habitus and SEM photographs, distribution maps, keys, and diagnoses of genera and species are provided. 相似文献
19.
Thomas Wesener Karin Voigtl?nder Peter Decker Jan Philip Oeyen J?rg Spelda 《ZooKeys》2016,(564):21-46
In order to evaluate the diversity of Central European Myriapoda species in the course of the German Barcode of Life project, 61 cytochrome c oxidase I sequences of the genus Cryptops Leach, 1815, a centipede genus of the order Scolopendromorpha, were successfully sequenced and analyzed. One sequence of Scolopendra
cingulata Latreille, 1829 and one of Theatops
erythrocephalus Koch, 1847 were utilized as outgroups. Instead of the expected three species (Cryptops
parisi Brolemann, 1920; Cryptops
anomalans Newport, 1844; Cryptops
hortensis (Donovan, 1810)), analyzed samples included eight to ten species. Of the eight clearly distinguishable morphospecies of Cryptops, five (Cryptops
parisi; Cryptops
croaticus Verhoeff, 1931; Cryptops
anomalans; Cryptops
umbricus Verhoeff, 1931; Cryptops
hortensis) could be tentatively determined to species level, while a further three remain undetermined (one each from Germany, Austria and Croatia, and Slovenia). Cryptops
croaticus is recorded for the first time from Austria. A single specimen (previously suspected as being Cryptops
anomalans), was redetermined as Cryptops
umbricus Verhoeff, 1931, a first record for Germany. All analyzed Cryptops species are monophyletic and show large genetic distances from one another (p-distances of 13.7–22.2%). Clear barcoding gaps are present in lineages represented by >10 specimens, highlighting the usefulness of the barcoding method for evaluating species diversity in centipedes. German specimens formally assigned to Cryptops
parisi are divided into three clades differing by 8.4–11.3% from one another; their intra-lineage genetic distance is much lower at 0–1.1%. The three clades are geographically separate, indicating that they might represent distinct species. Aside from Cryptops
parisi, intraspecific distances of Cryptops spp. in Central Europe are low (<3.3%). 相似文献
20.
Oobius Trjapitzin (Hymenoptera, Encyrtidae) species are egg parasitoids that are important for the biological control of some Buprestidae and Cerambycidae (Coleoptera). Two species, Oobius
agrili Zhang & Huang and Oobius
longoi (Siscaro), were introduced into North America for classical biocontrol and have successfully established. Two new native North American species that parasitize eggs of Agrilus spp. (Buprestidae) are described and illustrated from the USA: Oobius
minusculus Triapitsyn & Petrice, sp. n. (Michigan), an egg parasitoid of both Agrilus
subcinctus Gory on ash (Fraxinus spp.) and Agrilus
egenus Gory on black locust (Robinia
pseudoacacia L.) trees, and Oobius
whiteorum Triapitsyn, sp. n. (Pennsylvania), an egg parasitoid of Agrilus
anxius Gory on European white birch (Betula
pendula Roth). A taxonomic key and notes on the Nearctic native and introduced Oobius species are also included. 相似文献