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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.
César Román-Valencia Raquel I. Ruiz-C Donald C. Taphorn Carlos A. García-Alzate 《ZooKeys》2014,(454):109-125
Hemibrycon
sanjuanensis, new species, is described from the upper San Juan River drainage, Pacific versant, Colombia. It is distinguished from Hemibrycon
boquiae, Hemibrycon
brevispini, Hemibrycon
cairoense, Hemibrycon
colombianus, Hemibrycon
mikrostiktos, Hemibrycon
metae, Hemibrycon
palomae, Hemibrycon
rafaelense and Hemibrycon
tridens by the presence of a circular or oblong humeral spot that is located two scales posterior to the opercle (vs. 3–4 scales in Hemibrycon
palomae, Hemibrycon
rafaelense, Hemibrycon
brevispini and Hemibrycon
cairoense, and 0–1 scales, in Hemibrycon
metae and Hemibrycon
boquiae). It further differs from Hemibrycon
colombianus in having a round or oblong humeral spot (vs. rectangular). It differs from Hemibrycon
beni, Hemibrycon
dariensis, Hemibrycon
divisorensis, Hemibrycon
helleri, Hemibrycon
huambonicus, Hemibrycon
inambari, Hemibrycon
jabonero, Hemibrycon
jelskii, Hemibrycon
mikrostiktos, Hemibrycon
polyodon, Hemibrycon
quindos, Hemibrycon
raqueliae, Hemibrycon
santamartae, Hemibrycon
surinamensis, Hemibrycon
taeniurus, Hemibrycon
tridens, and Hemibrycon
yacopiae in having melanophores on the posterior margins of the scales along the sides of body (vs. lacking melanophores on margins of scales along entire length of the sides of body). The new species differs from all congeners mentioned above in having, among other features, six teeth in the outer premaxillary row arranged in a straight line (vs. five or fewer teeth not arranged in straight line except Hemibrycon
cairoense with two to six teeth in the outer premaxillary row). 相似文献
3.
The Neotropical genus Menevia Schaus, 1928 is revised to include 18 species, 11 of which are new. Two species, Menevia
ostia
comb. n. and Menevia
parostia
comb. n. are transferred from Pamea Walker, 1855 to Menevia. Four species-groups are diagnosed for the first time based on external characters and male genitalia morphology. The following new species are described: Menevia
rosea
sp. n., Menevia
torvamessoria
sp. n., Menevia
magna
sp. n., Menevia
menapia
sp. n., Menevia
mielkei
sp. n., Menevia
australis
sp. n., Menevia
vulgaris
sp. n., Menevia
franclemonti
sp. n., Menevia
vulgaricula
sp. n., Menevia
cordillera
sp. n., and Menevia
delphinus
sp. n.. A neotype is designated for Mimallo
plagiata Walker, 1855, which has since been placed in Menevia. Mimallo
saturata Walker, 1855 is interpreted to be a nomen dubium. 相似文献
4.
The type status is described for 65 taxa of the Orthalicoidea, classified within the families Megaspiridae (14), Orthalicidae (30), and Simpulopsidae (20); one taxon is considered a nomen inquirendum. Lectotypes are designated for the following taxa: Helix
brephoides d’Orbigny, 1835; Simpulopsis
cumingi Pfeiffer, 1861; Bulimulus (Protoglyptus) dejectus Fulton, 1907; Bulimus
iris Pfeiffer, 1853. The type status of Bulimus
salteri Sowerby III, 1890, and Strophocheilus (Eurytus) subirroratus da Costa, 1898 is now changed to lectotype according Art. 74.6 ICZN. The taxa Bulimus
loxostomus Pfeiffer, 1853, Bulimus
marmatensis Pfeiffer, 1855, Bulimus
meobambensis Pfeiffer, 1855, and Orthalicus
powissianus
var.
niveus
Preston 1909 are now figured for the first time. The following taxa are now considered junior subjective synonyms: Bulimus
marmatensis Pfeiffer, 1855 = Helix (Cochlogena) citrinovitrea Moricand, 1836; Vermiculatus Breure, 1978 = Bocourtia Rochebrune, 1882. New combinations are: Kuschelenia (Bocourtia) Rochebrune, 1882; Kuschelenia (Bocourtia) aequatoria (Pfeiffer, 1853); Kuschelenia (Bocourtia) anthisanensis (Pfeiffer, 1853); Kuschelenia (Bocourtia) aquila (Reeve, 1848); Kuschelenia (Bocourtia) badia (Sowerby I, 1835); Kuschelenia (Bocourtia) bicolor (Sowerby I, 1835); Kuschelenia (Bocourtia) caliginosa (Reeve, 1849); Kuschelenia (Bocourtia) coagulata (Reeve, 1849); Kuschelenia (Bocourtia) cotopaxiensis (Pfeiffer, 1853); Kuschelenia (Bocourtia) filaris (Pfeiffer, 1853); Kara
indentata (da Costa, 1901); Clathrorthalicus
magnificus (Pfeiffer, 1848); Simpulopsis (Eudioptus) marmartensis (Pfeiffer, 1855); Kuschelenia (Bocourtia) nucina (Reeve, 1850); Kuschelenia (Bocourtia) ochracea (Morelet, 1863); Kuschelenia (Bocourtia) peaki (Breure, 1978); Kuschelenia (Bocourtia) petiti (Pfeiffer, 1846); Clathrorthalicus
phoebus (Pfeiffer, 1863); Kuschelenia (Bocourtia) polymorpha (d’Orbigny, 1835); Scholvienia
porphyria (Pfeiffer, 1847); Kuschelenia (Bocourtia) purpurata (Reeve, 1849); Kuschelenia (Bocourtia) quechuarum Crawford, 1939; Quechua
salteri (Sowerby III, 1890); Kuschelenia (Bocourtia) subfasciata Pfeiffer, 1853; Clathrorthalicus
victor (Pfeiffer, 1854). In an addedum a lectotype is being designated for Bulimulus (Drymaeus) interruptus
var.
pallidus Preston, 1909. An index is included to all taxa mentioned in this paper and the preceding ones in this series (Breure and Ablett 2011, 2012, 2014). 相似文献
5.
90 species of Euplectrus are treated: 55 newly described, all from Area de Conservación Guanacaste (ACG), and 35 previously described species, of which 20 occur in ACG. Three of the previously described species (Euplectrus
brasiliensis Ashmead, Euplectrus
hircinus (Say), Euplectrus
ronnai (Brèthes)) have unknown status, owing to missing or severely damaged type material. The new species, all authored by C. Hansson, are: Euplectrus
alejandrovalerioi, Euplectrus
alexsmithi, Euplectrus
alvarowillei, Euplectrus
andybennetti, Euplectrus
andydeansi, Euplectrus
annettewalkerae, Euplectrus
billbrowni, Euplectrus
bobwhartoni, Euplectrus
carlosarmientoi, Euplectrus
carlrettenmeyeri, Euplectrus
charlesmicheneri, Euplectrus
charlesporteri, Euplectrus
chrisdarlingi, Euplectrus
chrisgrinteri, Euplectrus
corriemoreauae, Euplectrus
daveroubiki, Euplectrus
davesmithi, Euplectrus
davidwahli, Euplectrus
dianariasae, Euplectrus
donquickei, Euplectrus
eowilsoni, Euplectrus
garygibsoni, Euplectrus
gavinbroadi, Euplectrus
gerarddelvarei, Euplectrus
henrytownesi, Euplectrus
howelldalyi, Euplectrus
hugokonsi, Euplectrus
iangauldi, Euplectrus
jacklonginoi, Euplectrus
jesusugaldei, Euplectrus
jimwhitfieldi, Euplectrus
jjrodriguezae, Euplectrus
johnheratyi, Euplectrus
johnlasallei, Euplectrus
johnnoyesi, Euplectrus
josefernandezi, Euplectrus
lubomirmasneri, Euplectrus
markshawi, Euplectrus
mikegatesi, Euplectrus
mikeschauffi, Euplectrus
mikesharkeyi, Euplectrus
ninazitaniae, Euplectrus
pammitchellae, Euplectrus
paulhansoni, Euplectrus
paulheberti, Euplectrus
paulhurdi, Euplectrus
philwardi, Euplectrus
robbinthorpi, Euplectrus
ronaldzunigai, Euplectrus
roysnellingi, Euplectrus
scottshawi, Euplectrus
sondrawardae, Euplectrus
sydneycameronae, Euplectrus
victoriapookae, Euplectrus
wonyoungchoi. The species are described or redescribed, and thoroughly and uniformly illustrated, and included in two identification keys, one for females and one for males. Lectotypes are designated for eight species: Euplectrus
catocalae Howard (♂), Euplectrus
junctus Gahan (♀), Euplectrus
leucotrophis Howard (♂), Euplectrus
marginatus Ashmead (♀), Euplectrus
pachyscaphus Girault (♀), Euplectrus
platyhypenae Howard (♂), Euplectrus
semimarginatus Girault (♀), Heteroscapus
ronnai Brèthes (♂). One synonym is established: Euplectrus
walteri Schauff is a junior synonym of Euplectrus
testaceipes (Cameron). Brief image notes and host records are provided on the natural history of the wasps as well as the details of their morphology. Hosts are known for 74 Euplectrus species. 相似文献
6.
All genus-group names listed in the second edition of the catalogue (1833-1836) of Dejean’s beetle collection are recorded. For each new genus-group name the originally included available species are listed and for generic names with at least one available species, the type species and the current status are given. Names available prior to the publication of Dejean’s second catalogue (1833-1836) are listed in an appendix.The following new synonymies are proposed: Cyclonotum Dejean, 1833 (= Dactylosternum Wollaston, 1854) [Hydrophilidae], Hyporhiza Dejean, 1833 (= Rhinaspis Perty, 1830) [Scarabaeidae], Aethales Dejean, 1834 (= Epitragus Latreille, 1802) [Tenebrionidae], Arctylus Dejean, 1834 (= Praocis Eschscholtz, 1829) [Tenebrionidae], Euphron Dejean, 1834 (= Derosphaerus Thomson, 1858) [Tenebrionidae], Hipomelus Dejean, 1834 (= Trachynotus Latreille, 1828) [Tenebrionidae], Pezodontus Dejean, 1834 (= Odontopezus Alluaud, 1889) [Tenebrionidae], Zygocera Dejean, 1835 (= Disternopsis Breuning, 1939) [Cerambycidae], and Physonota Chevrolat, 1836 (= Anacassis Spaeth, 1913) [Chrysomelidae]. Heterogaster pilicornis Dejean, 1835 [Cerambycidae] and Labidomera trimaculata Chevrolat, 1836 [Chrysomelidae] are placed for the first time in synonymy with Anisogaster flavicans Deyrolle, 1862 and Chrysomela clivicollis Kirby, 1837 respectively. Type species of the following genus-group taxa are proposed: Sphaeromorphus Dejean, 1833 (Sphaeromorphus humeralis Erichson, 1843) [Scarabaeidae], Adelphus Dejean, 1834 (Helops marginatus Fabricius, 1792) [Tenebrionidae], Cyrtoderes Dejean, 1834 (Tenebrio cristatus DeGeer, 1778) [Tenebrionidae], Selenepistoma Dejean, 1834 (Opatrum acutum Wiedemann, 1823) [Tenebrionidae], Charactus Dejean, 1833 (Lycus limbatus Fabricius, 1801) [Lycidae], Corynomalus Chevrolat, 1836 (Eumorphus limbatus Olivier, 1808) [Endomychidae], Hebecerus Dejean, 1835 (Acanthocinus marginicollis Boisduval, 1835) [Cerambycidae], Pterostenus Dejean, 1835 (Cerambyx abbreviatus Fabricius, 1801) [Cerambycidae], Psalicerus Dejean, 1833 (Lucanus femoratus Fabricius, 1775) [Lucanidae], and Pygolampis Dejean, 1833 (Lampyris glauca Olivier, 1790) [Lampyridae]. A new name, Neoeutrapela Bousquet and Bouchard [Tenebrionidae], is proposed for Eutrapela Dejean, 1834 (junior homonym of Eutrapela Hübner, 1809).The following generic names, made available in Dejean’s catalogue, were found to be older than currently accepted valid names: Catoxantha Dejean, 1833 over Catoxantha Solier, 1833 [Buprestidae], Pristiptera Dejean, 1833 over Pelecopselaphus Solier, 1833 [Buprestidae], Charactus Dejean, 1833 over Calopteron Laporte, 1836 [Lycidae], Cyclonotum Dejean, 1833 over Dactylosternum Wollaston, 1854 [Hydrophilidae], Ancylonycha Dejean, 1833 over Holotrichia Hope, 1837 [Scarabaeidae], Aulacium Dejean, 1833 over Mentophilus Laporte, 1840 [Scarabaeidae], Sciuropus Dejean, 1833 over Ancistrosoma Curtis, 1835 [Scarabaeidae], Sphaeromorphus Dejean, 1833 over Ceratocanthus White, 1842 [Scarabaeidae], Psalicerus Dejean, 1833 over Leptinopterus Hope, 1838 [Lucanidae], Adelphus Dejean, 1834 over Praeugena Laporte, 1840 [Tenebrionidae], Amatodes Dejean, 1834 over Oncosoma Westwood, 1843 [Tenebrionidae], Cyrtoderes Dejean, 1834 over Phligra Laporte, 1840 [Tenebrionidae], Euphron Dejean, 1834 over Derosphaerus Thomson, 1858 [Tenebrionidae], Pezodontus Dejean, 1834 over Odontopezus Alluaud, 1889 [Tenebrionidae], Anoplosthaeta Dejean, 1835 over Prosopocera Blanchard, 1845 [Cerambycidae], Closteromerus Dejean, 1835 over Hylomela Gahan, 1904 [Cerambycidae], Hebecerus Dejean, 1835 over Ancita Thomson, 1864 [Cerambycidae], Mastigocera Dejean, 1835over Mallonia Thomson, 1857 [Cerambycidae], Zygocera Dejean, 1835 over Disternopsis Breuning, 1939 [Cerambycidae], Australica Chevrolat, 1836 over Calomela Hope, 1840 [Chrysomelidae], Edusa Chevrolat, 1836 over Edusella Chapuis, 1874 [Chrysomelidae], Litosonycha Chevrolat, 1836 over Asphaera Duponchel and Chevrolat, 1842 [Chrysomelidae], and Pleuraulaca Chevrolat, 1836 over Iphimeis Baly, 1864 [Chrysomelidae]. In each of these cases, Reversal of Precedence (ICZN 1999: 23.9) or an applicationto the International Commission on Zoological Nomenclature will be necessary to retain usage of the younger synonyms. 相似文献
7.
The Chinese species of the genera Omicrogiton Orchymont, 1919, Peratogonus Sharp, 1884 and Mircogioton Orchymont, 1937 are reviewed, diagnosed and keyed. Mircogioton and Omicrogiton are reported for the first time from China, Peratogonus for the first time for mainland China. Five species are recognized: Omicrogiton
coomani Balfour-Browne, 1939 (Guangdong, Hongkong), Omicrogiton
hainanensis
sp. n. (Hainan), Omicrogiton
roberti
sp. n. (Hainan), Mircogioton
coomani Orchymont, 1937 (Yunnan), and Peratogonus
reversus Sharp, 1884 (Guangdong, Jiangxi, Taiwan). Lectotype of Omicrogiton
coomani is designated. Mircogioton
cognitus (Malcolm, 1981), syn. n. is considered a junior subjective synonym of Mircogioton
coomani Orchymont, 1939. Species of Mircogioton and Omicrogiton inhabit decaying banana trunks, whereas Peratogonus
reversus was always collected from moist forest leaf litter. 相似文献
8.
9.
A new endemic genus and seven new species of New Zealand pselaphine staphylinid beetles of the supertribe Faronitae are described as follows: Pseudoexeirarthra Park & Carlton, gen. n. (type species: Sagola
spinifer Broun); Pseudoexeirarthra
sungmini Park & Carlton, sp. n.; Pseudoexeirarthra
kwangguki Park & Carlton, sp. n.; Pseudoexeirarthra
youngboki Park & Carlton, sp. n.; Pseudoexeirarthra
seiwoongi Park & Carlton, sp. n.; Pseudoexeirarthra
parkeri Park & Carlton, sp. n.; Pseudoexeirarthra
hlavaci Park & Carlton, sp. n.; Pseudoexeirarthra
nomurai Park & Carlton, sp. n. Three species, Sagola
spinifer Broun, Sagola
colorata Broun, and Sagola
puncticollis Broun, are transferred to the genus Pseudoexeirarthra. Six species are synonymized: Sagola
dilucida Broun, Sagola
guinnessi Broun, Sagola
longicollis Broun, Sagola
longula Broun, and Sagola
rectipennis Broun under Pseudoexeirarthra
spinifer (Broun); Sagola
insueta Broun under Sagola
colorata (Broun). A lectotype is designated for Pseudoexeirarthra
spinifer (Broun). A key, habitus photographs, line drawings of diagnostic characters, and distribution maps are provided for each species. 相似文献
10.
A critical and annotated catalogue of the ninety-six type specimens of Chrysididae (Hymenoptera), belonging to sixty-seven species, housed in the insect collection of Maximilian Spinola is given. The neotypes of six species are designated: Chrysis
bicolor Lepeletier, 1806; Chrysis
comparata Lepeletier, 1806; Chrysis
dives Dahlbom, 1854; Chrysis
pumila Klug, 1845; Chrysis
succincta Linnaeus, 1767; Hedychrum
bidentulum Lepeletier, 1806. The lectotypes of twenty-four species are designated: Chrysis
aequinoctialis Dahlbom, 1854; Chrysis
analis Spinola, 1808; Chrysis
assimilis Dahlbom, 1854; Chrysis
bihamata Spinola, 1838; Chrysis
chilensis Spinola, 1851; Chrysis
dichroa Dahlbom, 1854; Chrysis
distinguenda Dahlbom, 1854; Chrysis
episcopalis Spinola, 1838; Chrysis
grohmanni Dahlbom, 1854; Chrysis
incrassata Spinola, 1838; Chrysis
pallidicornis Spinola, 1838; Chrysis
pulchella Spinola, 1808; Chrysis
ramburi Dahlbom, 1854; Chrysis
refulgens Spinola, 1806; Chrysis
splendens Dahlbom, 1854; Chrysis
succinctula Dahlbom, 1854; Chrysis
versicolor Spinola, 1808; Elampus
gayi Spinola, 1851; Hedychrum
caerulescens Lepeletier, 1806; Hedychrum
chloroideum Dahlbom, 1854; Hedychrum
difficile Spinola, 1851; Hedychrum
virens Dahlbom, 1854; Holopyga
janthina Dahlbom, 1854; Holopyga
luzulina Dahlbom, 1854. Previous lectotype designations of five species are set aside: Chrysis
bicolor Lepeletier, 1806 (designated by Morgan 1984); Chrysis
calimorpha Mocsáry, 1882 (designated by Móczár 1965); Chrysis
elegans Lepeletier, 1806 (designated by Bohart (in Kimsey and Bohart 1991)); Hedychrum
chloroideum Dahlbom, 1854 (designated by Kimsey 1986); Hedychrum
rutilans Dahlbom, 1854 (designated by Morgan 1984). Three new synonymies are proposed: Hedychrum
intermedium Dahlbom, 1845, syn. n. of Holopyga
fervida (Fabricius, 1781); Chrysis
sicula Dahlbom, 1854, syn. n. of Chrysis
elegans Lepeletier, 1806; Chrysis
succinctula Dahlbom, 1854, syn. n. of Chrysis
germari Wesmael, 1839. Chrysis
distinguenda Spinola, 1838, and Chrysis
coronata Spinola, 1808, are considered nomina dubia.
Hedychrum
alterum Lepeletier, 1806, and Hedychrum
aulicum Spinola, 1843, are considered nomina oblita.
Hedychrum
rutilans Dahlbom, 1854, and Hedychrum
niemelai Linsenmaier, 1959, are retained as nomina protecta. The first available name for Chrysis
succinctula
sensu Linsenmaier is Chrysis
tristicula Linsenmaier, 1959, (stat. n.) The current status and validity of some types in the Spinola collection are discussed. Photographs of fifty-three types are given. 相似文献
11.
Paranastatus Masi, 1917 (Eupelmidae, Eupelminae) was originally described based on two species from Seychelles: Paranastatus
egregius and Paranastatus
violaceus. Eady (1956) subsequently described Paranastatus
nigriscutellatus and Paranastatus
verticalis from Fiji. Here, four new species of Paranastatus are described: Paranastatus
bellus Scallion, sp. n. and Paranastatus
pilosus Scallion, sp. n. from Indonesia, and Paranastatus
halko Scallion, sp. n. and Paranastatus
parkeri Scallion, sp. n. from Fiji. A key to all Paranastatus species based on females is included and lectotypes are designated for Paranastatus
egregius and Paranastatus
violaceus. Finally, previously unobserved colour variation from newly collected material of Paranastatus
verticalis, distribution patterns of species, and possibilities for future research are discussed. 相似文献
12.
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
13.
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
14.
15.
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
16.
Three species of the genus Xenocerogria Merkl, 2007 have been recorded in China, Xenocerogria
feai (Borchmann, 1911), Xenocerogria
ignota (Borchmann, 1941) and Xenocerogria
ruficollis (Borchmann, 1912). Xenocera
xanthisma Chen, 2002 is proposed as a junior synonym of Xenocerogria
ruficollis. Lectotype of Xenocerogria
ignota is designated, and the species is transferred to the genus Lagria Fabricius, 1775. New Chinese province records of Xenocerogria
ruficollis are provided. 相似文献
17.
The genus Liancalus Loew is revised for the Nearctic Region. Seven species are documented from this region including two new species: Liancalus
genualis Loew, Liancalus
hydrophilus Aldrich, Liancalus
limbatus Van Duzee, Liancalus
pterodactyl
sp. n., Liancalus
querulus Osten Sacken, Liancalus
similis Aldrich, and Liancalus
sonorus
sp. n. Lectotypes are designated for the following species: Liancalus
genualis, Liancalus
hydrophilus, Liancalus
querulus, and Liancalus
similis. The species are illustrated, a key to males and females is provided, and their distributions mapped. Adults of Liancalus are some of the largest species of Dolichopodidae and commonly occur on waterfalls and vertical seeps. 相似文献
18.
Alexander Riedel Rene T?nzler Michael Balke Cahyo Rahmadi Yayuk R. Suhardjono 《ZooKeys》2014,(467):1-162
The genus Trigonopterus Fauvel, 1862 is highly diverse in Melanesia. Only one species, Trigonopterus
amphoralis Marshall, 1925 was so far recorded West of Wallace’s Line (Eastern Sumatra). Based on focused field-work the fauna from Sundaland (Sumatra, Java, Bali, Palawan) and the Lesser Sunda Islands (Lombok, Sumbawa, Flores) is here revised. We redescribe Trigonopterus
amphoralis Marshall and describe an additional 98 new species: Trigonopterus
acuminatus
sp. n., Trigonopterus
aeneomicans
sp. n., Trigonopterus
alaspurwensis
sp. n., Trigonopterus
allopatricus
sp. n., Trigonopterus
allotopus
sp. n., Trigonopterus
angulicollis
sp. n., Trigonopterus
argopurensis
sp. n., Trigonopterus
arjunensis
sp. n., Trigonopterus
asper
sp. n., Trigonopterus
attenboroughi
sp. n., Trigonopterus
baliensis
sp. n., Trigonopterus
batukarensis
sp. n., Trigonopterus
bawangensis
sp. n., Trigonopterus
binodulus
sp. n., Trigonopterus
bornensis
sp. n., Trigonopterus
cahyoi
sp. n., Trigonopterus
costipennis
sp. n., Trigonopterus
cuprescens
sp. n., Trigonopterus
cupreus
sp. n., Trigonopterus
dacrycarpi
sp. n., Trigonopterus
delapan
sp. n., Trigonopterus
dentipes
sp. n., Trigonopterus
diengensis
sp. n., Trigonopterus
dimorphus
sp. n., Trigonopterus
disruptus
sp. n., Trigonopterus
dua
sp. n., Trigonopterus
duabelas
sp. n., Trigonopterus
echinatus
sp. n., Trigonopterus
empat
sp. n., Trigonopterus
enam
sp. n., Trigonopterus
fissitarsis
sp. n., Trigonopterus
florensis
sp. n., Trigonopterus
foveatus
sp. n., Trigonopterus
fulgidus
sp. n., Trigonopterus
gedensis
sp. n., Trigonopterus
halimunensis
sp. n., Trigonopterus
honjensis
sp. n., Trigonopterus
ijensis
sp. n., Trigonopterus
javensis
sp. n., Trigonopterus
kalimantanensis
sp. n., Trigonopterus
kintamanensis
sp. n., Trigonopterus
klatakanensis
sp. n., Trigonopterus
lampungensis
sp. n., Trigonopterus
latipes
sp. n., Trigonopterus
lima
sp. n., Trigonopterus
lombokensis
sp. n., Trigonopterus
merubetirensis
sp. n., Trigonopterus
mesehensis
sp. n., Trigonopterus
micans
sp. n., Trigonopterus
misellus
sp. n., Trigonopterus
palawanensis
sp. n., Trigonopterus
pangandaranensis
sp. n., Trigonopterus
paraflorensis
sp. n., Trigonopterus
pararugosus
sp. n., Trigonopterus
parasumbawensis
sp. n., Trigonopterus
pauxillus
sp. n., Trigonopterus
payungensis
sp. n., Trigonopterus
porcatus
sp. n., Trigonopterus
pseudoflorensis
sp. n., Trigonopterus
pseudosumbawensis
sp. n., Trigonopterus
punctatoseriatus
sp. n., Trigonopterus
ranakensis
sp. n., Trigonopterus
relictus
sp. n., Trigonopterus
rinjaniensis
sp. n., Trigonopterus
roensis
sp. n., Trigonopterus
rugosostriatus
sp. n., Trigonopterus
rugosus
sp. n., Trigonopterus
rutengensis
sp. n., Trigonopterus
saltator
sp. n., Trigonopterus
santubongensis
sp. n., Trigonopterus
sasak
sp. n., Trigonopterus
satu
sp. n., Trigonopterus
schulzi
sp. n., Trigonopterus
sebelas
sp. n., Trigonopterus
sembilan
sp. n., Trigonopterus
sepuluh
sp. n., Trigonopterus
seriatus
sp. n., Trigonopterus
serratifemur
sp. n., Trigonopterus
setifer
sp. n., Trigonopterus
silvestris
sp. n., Trigonopterus
singkawangensis
sp. n., Trigonopterus
singularis
sp. n., Trigonopterus
sinuatus
sp. n., Trigonopterus
squalidus
sp. n., Trigonopterus
sumatrensis
sp. n., Trigonopterus
sumbawensis
sp. n., Trigonopterus
sundaicus
sp. n., Trigonopterus
suturalis
sp. n., Trigonopterus
syarbis
sp. n., Trigonopterus
telagensis
sp. n., Trigonopterus
tepalensis
sp. n., Trigonopterus
tiga
sp. n., Trigonopterus
trigonopterus
sp. n., Trigonopterus
tujuh
sp. n., Trigonopterus
ujungkulonensis
sp. n., Trigonopterus
variolosus
sp. n., Trigonopterus
vulcanicus
sp. n., Trigonopterus
wallacei
sp. n.. All new species are authored by the taxonomist-in-charge, Alexander Riedel. Most species belong to the litter fauna of primary wet evergreen forests. This habitat has become highly fragmented in the study area and many of its remnants harbor endemic species. Conservation measures should be intensified, especially in smaller and less famous sites to minimize the number of species threatened by extinction. 相似文献
19.
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
20.
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