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1.
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
2.
The Australian species of the genus Trigonopterus Fauvel are revised. Eight previously recognized species are redescribed and 24 additional new species are described: Trigonopterus
allaetus Riedel, sp. n., Trigonopterus
athertonensis Riedel, sp. n., Trigonopterus
australinasutus Riedel, sp. n., Trigonopterus
australis Riedel, sp. n., Trigonopterus
bisignatus Riedel, sp. n., Trigonopterus
bisinuatus Riedel, sp. n., Trigonopterus
boolbunensis Riedel, sp. n., Trigonopterus
cooktownensis Riedel, sp. n., Trigonopterus
daintreensis Riedel, sp. n., Trigonopterus
deplanatus Riedel, sp. n., Trigonopterus
finniganensis Riedel, sp. n., Trigonopterus
fraterculus Riedel, sp. n., Trigonopterus
garradungensis Riedel, sp. n., Trigonopterus
hasenpuschi Riedel, sp. n., Trigonopterus
hartleyensis Riedel, sp. n., Trigonopterus
kurandensis Riedel, sp. n., Trigonopterus
lewisensis Riedel, sp. n., Trigonopterus
montanus Riedel, sp. n., Trigonopterus
monteithi Riedel, sp. n., Trigonopterus
mossmanensis Riedel, sp. n., Trigonopterus
oberprieleri Riedel, sp. n., Trigonopterus
robertsi Riedel, sp. n., Trigonopterus
terraereginae Riedel, sp. n., Trigonopterus
yorkensis Riedel, sp. n.. All new species are authored by the taxonomist-in-charge, Alexander Riedel. Lectotypes are designated for the following names: Idotasia
aequalis Pascoe, Idotasia
albidosparsa Lea, Idotasia
evanida Pascoe, Idotasia
laeta Lea, Idotasia
rostralis Lea, Idotasia
sculptirostris Lea, Idotasia
squamosa Lea. A new combination of the name Idotasia
striatipennis Lea is proposed: Trigonopterus
striatipennis (Lea), comb. n.. A key to the species is provided. Australian Trigonopterus occur in coastal Queensland, narrowly crossing into New South Wales. The southern parts of the range are inhabited by species found on foliage. A rich fauna of 19 edaphic species inhabiting the leaf litter of tropical forests is reported for the first time from the Australian Wet Tropics. 相似文献
3.
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
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.
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
6.
Thomas J. Henry 《ZooKeys》2015,(490):1-156
The Renodaeus group, a monophyletic assemblage of genera within the New World orthotyline tribe Ceratocapsini, comprising eight genera, including four new ones, is defined; and 48 species are treated, including 26 described as new and 12 transferred from Ceratocapsus Reuter as new combinations. Ceratocapsidea
gen. n. is described to accommodate the new species Ceratocapsidea
bahamaensis
sp. n., from the Bahamas; Ceratocapsidea
baranowskii
sp. n., from Jamaica; Ceratocapsidea
dominicanensis
sp. n., from the Dominican Republic; Ceratocapsidea
rileyi
sp. n., from Texas; Ceratocapsidea
taeniola
sp. n., from Jamaica; Ceratocapsidea
texensis
sp. n., from Texas; Ceratocapsidea
transversa
sp. n., from Mexico (Neuvo León); and Ceratocapsidea
variabilis
sp. n., from Jamaica; and Ceratocapsus
balli Knight, comb. n., Ceratocapsus
complicatus Knight, comb. n., Ceratocapsidea
consimilis Reuter, comb. n., Ceratocapsus
fusiformis Van Duzee, comb. n. (as the type species of the genus), Ceratocapsus
nigropiceus Reuter, comb. n., and Ceratocapsus
rufistigmus Blatchley, comb. n. [and a neotype designated], Ceratocapsus
clavicornis Knight, syn. n. and Ceratocapsus
divaricatus Knight, syn. n. are treated as junior synonyms of Ceratocapsus
fusiformis Van Duzee. The genus Marininocoris Carvalho and the only included species Marinonicoris
myrmecoides Carvalho are redescribed. The genus Pilophoropsis Poppius is redescribed and revised, Renodaeus
texanus Knight, comb. n. is transferred into it and the three new species Pilophoropsis
bejeanae
sp. n., from Sonora, Mexico; Pilophoropsis
cunealis
sp. n., from Oaxaca, Mexico; Pilophoropsis
quercicola
sp. n., from Arizona, USA, are described. Pilophoropsidea
gen. n. is described to accommodate the 12 new species Pilophoropsidea
brailovskyi
sp. n., from Federal District, Mexico; Pilophoropsidea
cuneata
sp. n., from Chiapas, Mexico; Pilophoropsidea
dimidiata
sp. n., from Durango, Mexico; Pilophoropsidea
fuscata
sp. n., from Durango, Mexico and Arizona and New Mexico, USA; Pilophoropsidea
keltoni
sp. n., from Durango, Mexico; Pilophoropsidea
maxima
sp. n., from Durango, Mexico; Pilophoropsidea
pueblaensis
sp. n., from Puebla, Mexico; Pilophoropsidea
schaffneri
sp. n., from Neuvo León and San Luis Potosi, Mexico; Pilophoropsidea
serrata
sp. n., from Michoacan, Mexico; Pilophoropsidea
touchetae
sp. n., from Mexico (Puebla); Pilophoropsidea
truncata
sp. n., from Mexico (Guerrero); Pilophoropsidea
tuberculata
sp. n., from Mexico (Guerrero); and Ceratocapsus
barberi Knight, comb. n., Ceratocapsus
camelus Knight, comb. n. (as the type species of the genus), and Ceratocapsus
fascipennis Knight, comb. n.
Pilophoropsita
gen. n. is described to accommodate Pilophoropsidea
schaffneri
sp. n. from Costa Rica and Mexico (Jalisco, Nayarit, Oaxaca). The genus Renodaeus Distant is redescribed and the new species Renodaeus
mimeticus
sp. n. from Ecuador is described. The genus Zanchisme Kirkaldy is reviewed and the four known species are redescribed. Zanchismeopsidea
gen. n. is described to accommodate Zanchismeopsidea
diegoi
sp. n. from Argentina (Santiago del Estero). Provided are habitus illustrations for certain adults (Pilophoropsidea
camelus, Pilophoropsis
brachyptera Poppius, Renodaeus
mimeticus, and Zanchisme
mexicanus Carvalho & Schaffner), male and female (when available) color digital images and figures of male genitalia of all species, electron photomicrographs of diagnostic characters for selected species, and keys to the genera and their included species. The taxa treated in this paper are arranged alphabetically by genus and species. 相似文献
7.
8.
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
9.
Tibor Németh Adél Tóth Judit Szenzenstein Péter Horváth Joshua D. Nosanchuk Zsuzsanna Grózer Renáta Tóth Csaba Papp Zsuzsanna Hamari Csaba Vágv?lgyi Attila Gácser 《PloS one》2013,8(7)
The C. parapsilosis sensu lato group involves three closely related species, C. parapsilosis sensu stricto,
C
. orthopsilosis
and
C
. metapsilosis
. Although their overall clinical importance is dramatically increasing, there are few studies regarding the virulence properties of the species of the psilosis complex. In this study, we tested 63 C. parapsilosis sensu stricto, 12
C
. metapsilosis
and 18
C
. orthopsilosis
isolates for the ability to produce extracellular proteases, secrete lipases and form pseudohyphae. Significant differences were noted between species, with the
C
. metapsilosis
strains failing to secrete lipase or to produce pseudohyphae. Nine different clinical isolates each of C. parapsilosis sensu stricto,
C
. orthopsilosis
and
C
. metapsilosis
were co-cultured with immortalized murine or primary human macrophages. C. parapsilosis sensu stricto isolates showed a significantly higher resistance to killing by primary human macrophages compared to
C
. orthopsilosis
and
C
. metapsilosis
isolates. In contrast, the killing of isolates by J774.2 mouse macrophages did not differ significantly between species. However, C. parapsilosis sensu stricto isolates induced the most damage to murine and human macrophages, and
C
. metapsilosis
strains were the least toxic. Furthermore, strains that produced lipase or pseudohyphae were most resistant to macrophage-mediated killing and produced the most cellular damage. Finally, we used 9 isolates of each of the C. parapsilosis sensus lato species to examine their impact on the survival of
Galleria
mellonella
larvae. The mortality rate of
G
. mellonella
larvae infected with
C
. metapsilosis
isolates was significantly lower than those infected with C. parapsilosis sensu stricto or
C
. orthopsilosis
strains. Taken together, our findings demonstrate that
C
. metapsilosis
is indeed the least virulent member of the psilosis group, and also highlight the importance of pseudohyphae and secreted lipases during fungal-host interactions. 相似文献
10.
Juan J. Morrone 《ZooKeys》2013,(273):15-71
The phylogenetic relationships of the genera of Listroderini LeConte, 1876 are analyzed based on 58 morphological characters. The genera are grouped in four clades, which are given subtribal status: Macrostyphlina new subtribe (Adioristidius, Amathynetoides, Andesianellus, Macrostyphlus, Nacodius and Puranius), Palaechthina Brinck, 1948 (Anorthorhinus, Gunodes, Haversiella, Inaccodes, Listronotus, Neopachytychius, Palaechthus, Palaechtodes, Steriphus and Tristanodes), Falklandiina new subtribe (Falklandiellus, Falklandiopsis, Falklandius, Gromilus, Lanteriella, Liparogetus, Nestrius and Telurus), and Listroderina (Acroriellus, Acrorius, Acrostomus, Antarctobius, Germainiellus, Hyperoides, Lamiarhinus, Listroderes, Methypora, Philippius, Rupanius and Trachodema). The subtribes are characterized and keys to identify them and their genera are provided. Listroderini have four main biogeographical patterns: Andean (Macrostyphlina), Andean-New Zealand (Falklandiina), Andean-Neotropical-Australian (Listroderina) and Andean-Neotropical-Australian-New Zealand-Nearctic-Tristan da Cunha-Gough islands (Palaechthina). Geographical paralogy, particularly evident in the Subantarctic subregion of the Andean region, suggests that Listroderini are an ancient Gondwanic group, in which several extinction events might have obscured relationships among the areas. 相似文献
11.
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
12.
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
13.
A critical and annotated catalogue of 72 types of Chrysididae (Hymenoptera) belonging to 53 species and subspecies housed in the Swedish Museum of Natural History is given. The lectotypes of Chrysis
diversa Dahlbom, 1845, Chrysis
soror Dahlbom, 1854, Chrysura
sulcata Dahlbom, 1845 and Holopyga
amoenula Dahlbom, 1845 are designated. The previous lectotype of Chrysis
diversa Dahlbom, 1845 is set aside. Five new synonymies are proposed: Chrysis
elegans
var.
smaragdula Trautmann, 1926 (currently Chrysis
elegans
ssp.
interrogata Linsenmaier, 1959 repl. name for smaragdula Trautmann, nec Fabricius, 1775), syn. n. of Chrysis
confluens (Dahlbom, 1845); Chrysis
eximia Mocsáry, 1889, syn. n. of Chrysis
poecila Mocsáry, 1889; Chrysis
pyrrhina Dahlbom, 1845, syn. n. of Chrysis
erythromelas Dahlbom, 1845; Chrysis
separata Trautmann, 1926, syn. n. of Chrysis
lateralis Dahlbom, 1845; Chrysis
sicula Abeille de Perrin, 1877, syn. n. of Chrysis
erythromelas Dahlbom, 1845. Chrysis
serena Radoszkowski, 1891 is the first available name for Chrysis
pyrrhina
sensu
auctorum. Chrysis
erythromelas Dahlbom, 1845 is revaluated as valid species. The neotype of Chrysis
inaequalis Dahlbom, 1845 is designated in the Linsenmaier collection (NMLS). Illustrations of 34 types are given. 相似文献
14.
The New World genus Philonome Chambers, 1874 is revised. This genus comprises twelve species, seven of which are described as new: two species, Philonome
nigrescens
sp. n. and Philonome
wielgusi
sp. n., from the United States; four species, Philonome
albivittata
sp. n., Philonome
curvilineata
sp. n., Philonome
kawakitai
sp. n., and Philonome
lambdagrapha
sp. n., from French Guiana; and one species, Philonome
penerivifera
sp. n., from Brazil. Lectotypes are designated for Philonome
clemensella Chambers, 1874 and Philonome
rivifera Meyrick, 1915. Partially on evidence of their head morphology and particularly from molecular evidence, the genus Philonome, previously associated with Bucculatricidae or Lyonetiidae, is reassigned to Tineidae. A possible systematic position of Philonome within Tineidae is discussed. Eurynome Chambers, 1875, is synonymized with Argyresthia Hübner, 1825 (Argyresthiidae). Photographs of adults and illustrations of genitalia, when available, are provided for all described species of Philonome and two species previously misplaced in Philonome, Argyresthia
luteella (Chambers, 1875) and Elachista
albella (Chambers, 1877). In addition, DNA barcodes were used for the delimitation of most species. 相似文献
15.
Bruno Massa 《ZooKeys》2015,(472):77-102
The results of the study of many specimens preserved in different European museums are reported. The tribe Terpnistrini Brunner von Wattenwyl, 1878 is resurrected. The distribution of the following species is enhanced: Pardalota
asymmetrica Karsch, 1896, Diogena
denticulata Chopard, 1954, Diogena
fausta (Burmeister, 1838), Plangiopsis
adeps Karsch, 1896, Poreuomena
sanghensis Massa, 2013 and Tylopsis
continua (Walker, 1869). Further, for their peculiar characteristics, two African representatives of the American genus Symmetropleura Brunner von Wattenwyl, 1878 are included in two new genera: Symmetrokarschia
africana (Brunner von Wattenwyl, 1878), comb. n. and Symmetroraggea
dirempta (Karsch, 1889), comb. n. A new genus and species from the Democratic Republic of Congo, Angustithorax
spiniger
gen. n., sp. n., and a new genus and species from Tanzania, Arostratum
oblitum
gen. n., sp. n. are described. Finally Melidia
claudiae
sp. n. and Atlasacris
brevipennis
sp. n. are described and compared with related species. 相似文献
16.
Gunnar Brehm 《ZooKeys》2015,(537):131-156
Three new Hagnagora Druce species (Geometridae, Larentiinae) are described: Hagnagora
richardi Brehm, sp. n. from Ecuador, Hagnagora
hedwigae Brehm, sp. n. from Ecuador, and Hagnagora
mirandahenrichae Brehm, sp. n. from Costa Rica. A checklist of taxa assigned to Hagnagora is provided. Hagnagora is provisionally divided into six clades: the anicata clade (6 species), the buckleyi clade (3 species), the croceitincta clade (3 species), the ephestris clade (3 species), the mortipax clade (4 species) and Hagnagora
subrosea (1 species). Two taxa are revived from synonymy: Hagnagora
catagrammina Druce, stat. rev. and Hagnagora
luteoradiata Thierry-Mieg, stat. rev. Two taxa are reinstated from subspecies to species level: Hagnagora
acothysta Schaus, stat. rev. and Hagnagora
jamaicensis Schaus, stat. rev. Four taxa are provisionally removed from Hagnagora: “Hagnagora” ignipennis, “Hagnagora” mesenata, “Hagnagora” vittata, and “Hagnagora” ceraria. After these changes, the genus Hagnagora now comprises 20 valid species. 相似文献
17.
18.
A checklist of the families Chaoboridae, Dixidae, Thaumaleidae, Psychodidae and Ptychopteridae (Diptera) recorded from Finland is given. Four species, Dixella
dyari Garret, 1924 (Dixidae), Threticus
tridactilis (Kincaid, 1899), Panimerus
albifacies (Tonnoir, 1919) and Panimerus
przhiboroi Wagner, 2005 (Psychodidae) are reported for the first time from Finland. 相似文献
19.
Helena Shaverdo Katayo Sagata Rawati Panjaitan Herlina Menufandu Michael Balke 《ZooKeys》2014,(468):1-83
Twenty three new species of Exocelina Broun, 1886 from New Guinea are described herein: Exocelina
bewaniensis
sp. n., Exocelina
bismarckensis
sp. n., Exocelina
craterensis
sp. n., Exocelina
gorokaensis
sp. n., Exocelina
herowana
sp. n., Exocelina
jimiensis
sp. n., Exocelina
kisli
sp. n., Exocelina
ksionseki
sp. n., Exocelina
lembena
sp. n., Exocelina
mantembu
sp. n., Exocelina
michaelensis
sp. n., Exocelina
pinocchio
sp. n., Exocelina
pseudoastrophallus
sp. n., Exocelina
pseudobifida
sp. n., Exocelina
pseudoedeltraudae
sp. n., Exocelina
pseudoeme
sp. n., Exocelina
sandaunensis
sp. n., Exocelina
simbaiarea
sp. n., Exocelina
skalei
sp. n., Exocelina
tabubilensis
sp. n., Exocelina
tariensis
sp. n., Exocelina
vovai
sp. n., and Exocelina
wannangensis
sp. n. All of them have been found to belong to the Exocelina
ekari-group. An identification key to all known species of the group is provided, and important diagnostic characters (habitus, color, male antennae, protarsomeres 4–5, median lobes, and parameres) are illustrated. Data on the distribution of the new species and some already described species are given. 相似文献
20.
Sergei I. Golovatch Jean-Jacques Geoffroy Jean-Paul Mauriès Didier VandenSpiegel 《ZooKeys》2015,(505):1-34
The Eutrichodesmus fauna of mainland China, by far the largest genus in the Indo-Australian family Haplodesmidae, is reviewed and shown to encompass 23 species (of a total of 45), all keyed. The following nine new species, all presumed troglobites, are described: Eutrichodesmus
triangularis
sp. n., from Sichuan, Eutrichodesmus
lipsae
sp. n., from Guangxi, Eutrichodesmus
tenuis
sp. n., Eutrichodesmus
trontelji
sp. n., Eutrichodesmus
latellai
sp. n., Eutrichodesmus
obliteratus
sp. n. and Eutrichodesmus
troglobius
sp. n., all from Guizhou, Eutrichodesmus
sketi
sp. n., from Hunan, and Eutrichodesmus
apicalis
sp. n., from Hubei. 相似文献