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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.
3.
Reginald P. Webster Chantelle A. Alderson Vincent L. Webster CoryC. Hughes Jon D. Sweeney 《ZooKeys》2016,(552):109-122
Sixteen species of Cerambycidae are newly recorded for New Brunswick, Canada; Arhopalus
obsoletus (Randall), Atimia
confusa
confusa (Say), Callidium
frigidum Casey, Phymatodes
amoenus (Say), Phymatodes
testaceus (Linnaeus), Neoclytus
mucronatus
mucronatus (Fabricius), Xylotrechus
aceris Fisher, Xylotrechus
sagittatus
sagittatus (Germar), Tylonotus
bimaculatus Haldeman, Lepturges
angulatus (LeConte), Lepturges
symmetricus (Haldeman), Urgleptes
querci (Fitch), Oplosia
nubila (LeConte), Eupogonius
subarmatus (LeConte), Monochamus
carolinensis (Olivier), and Pogonocherus
parvulus LeConte. Urgleptes
signatus (LeConte) and Urgleptes
querci are newly recorded from Nova Scotia. All but two specimens were collected in 12-funnel Lindgren traps. Xylotrechus
aceris, Tylonotus
bimaculatus, Lepturges
angulatus, Lepturges
symmetricus, Urgleptes
signatus (NS), and Pogonocherus
parvulus were detected exclusively in traps deployed in the forest canopy, and most individuals of Oplosia
nubila and Monochamus
carolinensis were captured in canopy traps. Arhopalus
obsoletus, Atimia
confusa
confusa, Callidium
frigidum, Phymatodes
testaceus, and Xylotrechus
sagittatus
sagittatus were captured almost exclusively in traps near (1 m above) the forest floor. These results highlight the importance of sampling both the understory and upper canopy when using traps for surveying diversity of Cerambycidae. 相似文献
4.
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
5.
B. Christian Schmidt 《ZooKeys》2015,(527):103-126
The Lacinipolia
vicina (Grote) species complex, previously consisting of Lacinipolia
vicina, Lacinipolia
teligera (Morrison), Lacinipolia
pensilis (Grote), and Lacinipolia
subalba Mustelin is revised to six species: Lacinipolia
vicina (eastern USA), Lacinipolia
teligera (southern Great Plains), Lacinipolia
pensilis (Pacific Northwest and northern Rocky Mountains), Lacinipolia
acutipennis (Grote), stat. rev. (= Lacinipolia
subalba
syn. n.) (western North America), Lacinipolia
sareta (Smith), stat. rev. (Canada and western USA) and Lacinipolia
dimocki, sp. n. (California and Pacific Northwest). Lectotypes are designated for Lacinipolia
vicina, Lacinipolia
teligera and Lacinipolia
pensilis. 相似文献
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
13.
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
14.
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
15.
Eight new genera and 30 new species are described: Cirrosus
gen. n. (type species Cirrosus
atrocaudatus
sp. n. (♂♀)), Conglin
gen. n. (type species Conglin
personatus
sp. n. (♀)), Curtimeticus
gen. n. (type species Curtimeticus
nebulosus
sp. n. (♂)), Gladiata
gen. n. (type species Gladiata
fengli
sp. n. (♂)), Glebala
gen. n. (type species Glebala
aspera
sp. n. (♂)), Glomerosus
gen. n. (type species Glomerosus
lateralis
sp. n. (♂)), Smerasia
gen. n. (type species Smerasia
obscurus
sp. n. (♂♀)), Vittatus
gen. n. (type species Vittatus
fencha
sp. n. (♂♀)); Batueta
cuspidata
sp. n. (♂♀), Capsulia
laciniosa
sp. n. (♂), Dactylopisthes
separatus
sp. n. (♀), Gongylidiellum
bracteatum
sp. n. (♀), Houshenzinus
xiaolongha
sp. n. (♂♀), Laogone
bai
sp. n. (♂), Laogone
lunata
sp. n. (♂♀), Maro
bulbosus
sp. n. (♀), Nasoonaria
circinata
sp. n. (♂♀), Neriene
circifolia
sp. n. (♂♀), Oedothorax
biantu
sp. n. (♀), Oilinyphia
hengji
sp. n. (♂♀), Paikiniana
furcata
sp. n. (♂♀), Parameioneta
bishou
sp. n. (♂♀), Parameioneta
multifida
sp. n. (♂♀), Parameioneta
tricolorata
sp. n. (♂♀), Tapinopa
undata
sp. n. (♂), Theoa
bidentata
sp. n. (♂♀), Theoa
vesica
sp. n. (♂♀), Vittatus
bian
sp. n. (♂♀), Vittatus
latus
sp. n. (♂♀), Vittatus
pan
sp. n. (♂♀). The male of Kaestneria
bicultrata Chen & Yin, 2000 and the females of Asiagone
perforata Tanasevitch, 2014 and Batueta
similis Wunderlich & Song, 1995 are described for the first time; photos of Bathyphantes
paracymbialis Tanasevitch, 2014 are provided. 相似文献
16.
17.
18.
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
19.
The cotton aphid, Aphis
gossypii, is one of the most biologically diverse species of aphids; a polyphagous species in a family where most are host specialists. It is economically important and belongs to a group of closely related species that has challenged aphid taxonomy. The research presented here seeks to clarify the taxonomic relationships and status of species within the Aphid
gossypii group in the North American Midwest. Sequences of the mitochondrial cytochrome oxidase 1 (COI), nuclear elongation factor 1-α (EF1-α), and nuclear sodium channel para-type (SCP) genes were used to differentiate between Aphid
gossypii and related species. Aphis
monardae, previously synonymised with Aphid
gossypii, is re-established as a valid species. Phylogenetic analyses support the close relationship of members of the Aphid
gossypii group native to North America (Aphid
forbesi, Aphid
monardae, Aphid
oestlundi, Aphid
rubifolii, and Aphid
rubicola), Europe (Aphid
nasturtii, Aphid
urticata and Aphid
sedi), and Asia (Aphid
agrimoniae, Aphid
clerodendri, Aphid
glycines, Aphid
gossypii, Aphid
hypericiphaga, Aphid
ichigicola, Aphid
ichigo, Aphid
sanguisorbicola, Aphid
sumire and Aphid
taraxicicola). The North American species most closely related to Aphid
gossypii are Aphid
monardae and Aphid
oestlundi. The cosmopolitan Aphid
gossypii and Aphid
sedi identified in the USA are genetically very similar using COI and EF1-α sequences, but the SCP gene shows greater genetic distance between them. We present a discussion of the biological and morphological differentiation of these species. 相似文献
20.