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1.
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
2.
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.
Mi?osz A. Mazur 《ZooKeys》2016,(554):87-118
The genus Rasilinus
gen. n. is described (type species Rasilinus
tchambicus sp. n.). Nine new species: Rasilinus
bicolor
sp. n., Rasilinus
bifurcatus
sp. n., Rasilinus
bimaculatus
sp. n., Rasilinus
grandidens
sp. n., Rasilinus
longulus
sp. n., Rasilinus
subgemellus
sp. n., Rasilinus
subnodulus
sp. n., Rasilinus
tchambicus
sp. n., Rasilinus
virgatus
sp. n. are described from New Caledonia. Illustrations of the external morphology, male and female terminalia, dorsal habitus colour photographs of the adults, key to species and distribution map of the new genus Rasilinus are provided. 相似文献
5.
Genomic constitution and taxonomy of the Chinese hexaploids Elymus cylindricus and E. breviaristatus (Poaceae: Triticeae) 下载免费PDF全文
Cai‐Rong Yang Bernard‐R. Baum Wei‐Huan Chen Hai‐Qin Zhang Xiao‐Yan Liu Xing Fan Li‐Na Sha Hou‐Yang Kang Yi Wang Yong‐Hong Zhou 《Botanical journal of the Linnean Society. Linnean Society of London》2016,182(3):650-657
Elymus cylindricus (2n = 6x = 42) and E. breviaristatus (2n = 6x = 42) are distributed in grasslands and deserts of northern and north‐western China. Their genomic constitution and taxonomic status are unclear. Elymus cylindricus was crossed with E. wawawaiensis J.R.Carlson & Barkworth ( StH ), Roegneria grandis Keng ( StY ) and Campeiostachys dahurica (Turcz. ex Griseb.) B.R.Baum, J.L. Y ang & C. Y en var. dahurica ( StYH ). Meiotic pairing in the hybrids E. cylindricus × E. wawawaiensis ( StH ), E. cylindricus × R. grandis ( StY ) and E. cylindricus × C. dahurica var. dahurica ( StYH ) showed on average 10.00, 11.30 and 20.92 bivalents per cell, respectively. Elymus breviaristatus was crossed with C. dahurica var. dahurica ( StYH ) and E. cylindricus. Chromosome pairing in the hybrids of E. breviaristatus × C. dahurica var. dahurica and E. breviaristatus × E. cylindricus showed on average 19.60 and 19.27 bivalents, respectively. Genomic in situ hybridization (GI SH ) revealed the presence of St , Y and H genomes in E. cylindricus and E. breviaristatus. An intergenomic rearrangement was observed in E. cylindricus using GI SH . Meiotic pairing data and GI SH indicated that both E. cylindricus and E. breviaristatus are allohexaploids containing the StYH genomes. Elymus cylindricus and E. breviaristatus should be treated as Campeiostachys dahurica var. cylindrica and Campeiostachys breviaristata, respectively. 相似文献
6.
The results of genome analysis of five hybrids, viz.Elymus patagonicus ×Hordeum procerum, E. patagonicus ×H. tetraploidum, E. angulatus ×H. jubatum, E. angulatus ×H. lechleri, andE. angulatus ×H. parodii, are reported. The genomic constitution ofHordeum tetraploidum andH. jubatum is best given as H1H1H2H2, ofH. lechleri andH. parodii as H1H1H2H2H4H4, ofH. procerum as H1H1H2H2H3H3, and ofElymus patagonicus andE. angulatus as SSH1H1H2H2. 相似文献
7.
Ohne ZusammenfassungZeichenerklärung
Aa
Augenanlage
-
Abs
Abdominalsegment 1–6
-
äG
äußeres Ganglion
-
Ak
Augenkapsel
-
Akb
Augenkapselbildungszellen
-
ä.Kr.
Äeßere Kreuzung
-
Bm
Basalmembran
-
Bz.
Basalzelle
-
Dv
Dorsalverfalzung
-
El
Elytre
-
Fe
Femur
-
Fg
Fettgewebe
-
GZ
Ganglienzellen
-
GMZ
Ganglienmutterzellen
-
HBH
hinterer Bildungsherd
-
HC
hintere Coxa
-
HPZ
Hauptpigmentzellen
-
Hy
Hypodormis
-
HZ
Stützzellen
-
Z
Imaginalscheibe
-
i.G.
inneres Ganglion
-
i.Kr.
innere Kreuzung
-
K
Kornea
-
KK
Kristallkegel
-
KKZ
Kristallkegelzellen
-
KZ
Korneagenzellen
-
LH
Lamellenhaare
-
MC
mittlere Coxa
-
MG
mittleres Ganglion
-
Neur
Neuroblast
-
Nf
Nervenfaser
-
N.opt.
Nervus opticus (Nervenbündelschict)
-
NPZ
Nebenpigmentzellen
-
N.st.
Nervus stemmaticus
-
o.A.
oberes Auge
-
P.
Punkte auf den Elytren mit Chitinzapfen
-
Ph
Phagozyten
-
R.
Rhabdom
-
Ret
Retinula
-
RZK
Retinulazellkerne
-
Ret.Z.
Retinulazellen
-
r.f.
Musculus rotator femuris
-
rud. St.
rudimentäre Stemmata
-
SZ
Sehzellen
-
S.V.
seitliche Verfalzung
-
Ta 1–4
Tarsus 1–4
-
Ti
Tibia
-
Ti.T.
Tibialtasche
-
Tr.
Trachee
-
u.A.
Unteres Auge
-
V.C.
vordere Coxa
-
VBH
vorderer Bildungsherd
-
Z
Zuwachszone
-
ZG
Zellgrenze 相似文献
8.
9.
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
10.
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
11.
The genera Odontacolus Kieffer and Cyphacolus Priesner are among the most distinctive platygastroid wasps because of their laterally compressed metasomal horn; however, their generic status has remained unclear. We present a morphological phylogenetic analysis comprising all 38 Old World and four Neotropical Odontacolus species and 13 Cyphacolus species, which demonstrates that the latter is monophyletic but nested within a somewhat poorly resolved Odontacolus. Based on these results Cyphacolus
syn. n. is placed as a junior synonym of Odontacolus which is here redefined. The taxonomy of Old World Odontacolus
s.str. is revised; the previously known species Odontacolus longiceps Kieffer (Seychelles), Odontacolus markadicus Veenakumari (India), Odontacolus spinosus (Dodd) (Australia) and Odontacolus hackeri (Dodd) (Australia) are re-described, and 32 new species are described: Odontacolus africanus Valerio & Austin sp. n. (Congo, Guinea, Kenya, Madagascar, Mozambique, South Africa, Uganda, Zimbabwe), Odontacolus aldrovandii Valerio & Austin sp. n. (Nepal), Odontacolus anningae Valerio & Austin sp. n. (Cameroon), Odontacolus australiensis Valerio & Austin sp. n. (Australia), Odontacolus baeri Valerio & Austin sp. n. (Australia), Odontacolus berryae Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus bosei Valerio & Austin sp. n. (India, Malaysia, Sri Lanka), Odontacolus cardaleae Valerio & Austin sp. n. (Australia), Odontacolus darwini Valerio & Austin sp. n. (Thailand), Odontacolus dayi Valerio & Austin sp. n. (Indonesia), Odontacolus gallowayi Valerio & Austin sp. n. (Australia), Odontacolus gentingensis Valerio & Austin sp. n. (Malaysia), Odontacolus guineensis Valerio & Austin sp. n. (Guinea), Odontacolus harveyi Valerio & Austin sp. n. (Australia), Odontacolus heratyi Valerio & Austin sp. n. (Fiji), Odontacolus heydoni Valerio & Austin sp. n. (Malaysia, Thailand), Odontacolus irwini Valerio & Austin sp. n. (Fiji), Odontacolus jacksonae Valerio & Austin sp. n. (Cameroon, Guinea, Madagascar), Odontacolus kiau Valerio & Austin sp. n. (Papua New Guinea), Odontacolus lamarcki Valerio & Austin sp. n. (Thailand), Odontacolus madagascarensis Valerio & Austin sp. n. (Madagascar), Odontacolus mayri Valerio & Austin sp. n. (Indonesia, Thailand), Odontacolus mot Valerio & Austin sp. n. (India), Odontacolus noyesi Valerio & Austin sp. n. (India, Indonesia), Odontacolus pintoi Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus schlingeri Valerio & Austin sp. n. (Fiji), Odontacolus sharkeyi Valerio & Austin sp. n. (Thailand), Odontacolus veroae Valerio & Austin sp. n. (Fiji), Odontacolus wallacei Valerio & Austin sp. n. (Australia, Indonesia, Malawi, Papua New Guinea), Odontacolus whitfieldi Valerio & Austin sp. n. (China, India, Indonesia, Sulawesi, Malaysia, Thailand, Vietnam), Odontacolus zborowskii Valerio & Austin sp. n. (Australia), and Odontacolus zimi Valerio & Austin sp. n. (Madagascar). In addition, all species of Cyphacolus are here transferred to Odontacolus: Odontacolus asheri (Valerio, Masner & Austin) comb. n. (Sri Lanka), Odontacolus axfordi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus bhowaliensis (Mani & Mukerjee) comb. n. (India), Odontacolus bouceki (Austin & Iqbal) comb. n. (Australia), Odontacolus copelandi (Valerio, Masner & Austin) comb. n. (Kenya, Nigeria, Zimbabwe, Thailand), Odontacolus diazae (Valerio, Masner & Austin) comb. n. (Kenya), Odontacolus harteni (Valerio, Masner & Austin) comb. n. (Yemen, Ivory Coast, Paskistan), Odontacolus jenningsi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus leblanci (Valerio, Masner & Austin) comb. n. (Guinea), Odontacolus lucianae (Valerio, Masner & Austin) comb. n. (Ivory Coast, Madagascar, South Africa, Swaziland, Zimbabwe), Odontacolus normani (Valerio, Masner & Austin) comb. n. (India, United Arab Emirates), Odontacolus sallyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tessae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tullyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus veniprivus (Priesner) comb. n. (Egypt), and Odontacolus watshami (Valerio, Masner & Austin) comb. n. (Africa, Madagascar). Two species of Odontacolus are transferred to the genus Idris Förster: Idris longispinosus (Girault) comb. n. and Idris amoenus (Kononova) comb. n., and Odontacolus doddi Austin syn. n. is placed as a junior synonym of Odontacolus spinosus (Dodd). Odontacolus markadicus, previously only known from India, is here recorded from Brunei, Malaysia, Sri Lanka, Thailand and Vietnam. The relationships, distribution and biology of Odontacolus are discussed, and a key is provided to identify all species. 相似文献
12.
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
13.
Two Issini genera, Sarima Melichar, 1903 and Sarimodes Matsumura, 1916, are examined. One new Sarima species: Sarima
bifurcus
sp. n. and two new Sarimodes species Sarimodes
clavatus
sp. n. and Sarimodes
parallelus
sp. n. are added from South China. A checklist of species in the genus Sarima with data on distribution is provided. The distribution and morphological peculiarities of the genera Sarima and Sarimodes are briefly discussed. 相似文献
14.
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
15.
Six new species of the spider genus Spiricoelotes Wang, 2002 are described, Spiricoelotes
anshiensis Chen & Li, sp. n. (♂♀), Spiricoelotes
chufengensis Chen & Li, sp. n. (♂♀), Spiricoelotes
nansheensis Chen & Li, sp. n. (♂♀), Spiricoelotes
taipingensis Chen & Li, sp. n. (♂♀), Spiricoelotes
xianheensis Chen & Li, sp. n. (♂♀) and Spiricoelotes
xiongxinensis Chen & Li, sp. n. (♀). All new species were collected from caves in Jiangxi Province, China. 相似文献
16.
Shah, Ashish R., Thomas G. Keens, and David Gozal.Effect of supplemental oxygen on supramaximal exercise performance and recovery in cystic fibrosis. J. Appl.Physiol. 83(5): 1641-1647, 1997.The effects ofsupplemental O2 on recovery fromsupramaximal exercise and subsequent performance remain unknown. Ifrecovery from exercise could be enhanced in individuals with chroniclung disease, subsequent supramaximal exercise performance could also be improved. Recovery from supramaximal exercise and subsequent supramaximal exercise performance were assessed after 10 min of breathing 100% O2 or room air(RA) in 17 cystic fibrosis (CF) patients [25 ± 10 (SD) yrold, 53% men, forced expired volume in 1 s = 62 ± 21%predicted] and 17 normal subjects (25 ± 8 yr old, 59% men,forced expired volume in 1 s = 112 ± 15% predicted). Supramaximalperformance was assessed as the work of sustained bicycling at a loadof 130% of the maximum load achieved during a graded maximal exercise.Peak minute ventilation(E) andheart rate (HR) were lower in CF patients at the end of eachsupramaximal bout than in controls. In CF patients, single-exponentialtime decay constants indicated faster recovery of HR(HR = 86 ± 8 and 73 ± 6 s in RA and O2,respectively, P < 0.01). Similarly, fast and slow time constants of two-exponential equations providing thebest fit for ventilatory recovery were improved in CF patients duringO2 breathing ( = 132.1 ± 10.5 vs. 82.5 ± 10.4 s; = 880.3 ± 300.1 vs. 368.6 ± 107.1 s,P < 0.01). However, no such improvements occurred in controls. Supramaximal performance after O2 improved in CF patients (109 ± 6% of the 1st bout after O2 vs. 94 ± 6% in RA, P < 0.01).O2 supplementation had no effect on subsequent performance in controls (97 ± 3% inO2 vs. 93 ± 3% in RA). Weconclude that supplemental O2after a short bout of supramaximal exercise accelerates recovery andpreserves subsequent supramaximal performance in patients with CF. 相似文献
17.
Robert Mesibov 《ZooKeys》2013,(325):33-64
The genus Agathodesmus Silvestri, 1910 is speciose and widespread in high-rainfall parts of eastern Australia. In addition to the type species Agathodesmus steeli Silvestri, 1910 and Agathodesmus johnsi Mesibov, 2009 from New South Wales and Agathodesmus bucculentus (Jeekel, 1986) from Queensland, the following 18 new species are recognised: Agathodesmus adelphus
sp. n., Agathodesmus aenigmaticus
sp. n., Agathodesmus agnus
sp. n., Agathodesmus anici
sp. n., Agathodesmus gayundah
sp. n., Agathodesmus hahnensis
sp. n., Agathodesmus kerensis
sp. n., Agathodesmus kirrama
sp. n., Agathodesmus millaa
sp. n., Agathodesmus parapholeus
sp. n., Agathodesmus quintanus
sp. n., Agathodesmus sagma
sp. n., Agathodesmus summus
sp. n. and Agathodesmus yuccabinensis
sp. n. from Queensland; Agathodesmus carorum
sp. n. from New South Wales and Victoria; Agathodesmus bonang
sp. n. and Agathodesmus morwellensis
sp. n. from Victoria; and Agathodesmus chandleri
sp. n. from South Australia. 相似文献
18.
19.
The species of the subfamily Opiinae (Hymenoptera: Braconidae) from Hunan (Oriental China) are revised and illustrated. Thirty-six new species are described: Apodesmia bruniclypealis Li & van Achterberg, sp. n., Apodesmia melliclypealis Li & van Achterberg, sp. n., Areotetes albiferus Li & van Achterberg, sp. n., Areotetes carinuliferus Li & van Achterberg, sp. n., Areotetes striatiferus Li & van Achterberg, sp. n., Coleopioides diversinotum Li & van Achterberg, sp. n., Coleopioides postpectalis Li & van Achterberg, sp. n., Fopius dorsopiferus Li, van Achterberg & Tan, sp. n., Indiopius chenae Li & van Achterberg, sp. n., Opiognathus aulaciferus Li & van Achterberg, sp. n., Opiognathus brevibasalis Li & van Achterberg, sp. n., Opius crenuliferus Li & van Achterberg, sp. n., Opius malarator Li, van Achterberg & Tan, sp. n., Opius monilipalpis Li & van Achterberg, sp. n., Opius pachymerus Li & van Achterberg, sp. n., Opius songi Li & van Achterberg, sp. n., Opius youi Li & van Achterberg, sp. n., Opius zengi Li & van Achterberg, sp. n., Phaedrotoma acuticlypeata Li & van Achterberg, sp. n., Phaedrotoma angiclypeata Li & van Achterberg, sp. n., Phaedrotoma antenervalis Li & van Achterberg, sp. n., Phaedrotoma depressiclypealis
Li & van Achterberg, sp. n., Phaedrotoma flavisoma Li & van Achterberg, sp. n., Phaedrotoma nigrisoma Li & van Achterberg, sp. n., Phaedrotoma protuberator Li & van Achterberg, sp. n., Phaedrotoma rugulifera Li & van Achterberg, sp. n., Li & van Achterberg,Phaedrotoma striatinota Li & van Achterberg, sp. n., Phaedrotoma vermiculifera Li & van Achterberg, sp. n., Rhogadopsis latipennis Li & van Achterberg, sp. n.,
Rhogadopsis longicaudifera Li & van Achterberg, sp. n., Rhogadopsis maculosa Li, van Achterberg & Tan, sp. n., Rhogadopsis obliqua Li & van Achterberg, sp. n., Rhogadopsis sculpturator Li & van Achterberg, sp. n., Utetes longicarinatus Li & van Achterberg, sp. n. and Xynobius notauliferus Li & van Achterberg, sp. n.
Areotetes van Achterberg & Li, gen. n. (type species: Areotetes carinuliferus
sp. n.) and Coleopioides van Achterberg & Li, gen. n. (type species: Coleopioides postpectalis
sp. n. are described. All species are illustrated and keyed. In total 30 species of Opiinae are sequenced and the cladograms are presented. Neopius Gahan, 1917, Opiognathus Fischer, 1972, Opiostomus Fischer, 1972, and Rhogadopsis Brèthes, 1913, are treated as a valid genera based on molecular and morphological differences. Opius vittata Chen & Weng, 2005 (not Opius vittatus Ruschka, 1915), Opius ambiguus Weng & Chen, 2005 (not Wesmael, 1835) and Opius mitis Chen & Weng, 2005 (not Fischer, 1963) are primary homonymsandarerenamed into Phaedrotoma depressa Li & van Achterberg, nom. n., Opius cheni Li & van Achterberg, nom. n. andOpius wengi Li & van Achterberg, nom. n., respectively. Phaedrotoma terga (Chen & Weng, 2005) comb. n.,Diachasmimorpha longicaudata (Ashmead, 1905) and Biosteres pavitita Chen & Weng, 2005, are reported new for Hunan, Opiostomus aureliae (Fischer, 1957) comb. n. is new for China and Hunan; Xynobius maculipennis(Enderlein, 1912) comb. n. is new for Hunan and continental China and Rhogadopsis longuria (Chen & Weng, 2005) comb. n. is new for Hunan. The following new combinations are given: Apodesmia puncta (Weng & Chen, 2005) comb. n., Apodesmia tracta (Weng & Chen, 2005) comb. n., Areotetes laevigatus (Weng & Chen, 2005) comb. n., Phaedrotoma dimidia (Chen & Weng, 2005) comb. n., Phaedrotoma improcera (Weng & Chen, 2005) comb. n., Phaedrotoma amputata (Weng & Chen, 2005) comb. n., Phaedrotoma larga (Weng & Chen, 2005) comb. n., Phaedrotoma osculas (Weng & Chen, 2005) comb. n., Phaedrotoma postuma (Chen & Weng, 2005) comb. n., Phaedrotoma rugulosa (Chen & Weng, 2005) comb. n., Phaedrotoma tabularis (Weng & Chen, 2005) comb. n., Rhogadopsis apii (Chen & Weng, 2005) comb. n., Rhogadopsis dimidia (Chen & Weng, 2005) comb. n.,
Rhogadopsis diutia (Chen & Weng, 2005) comb. n., Rhogadopsis longuria (Chen & Weng, 2005) comb. n., Rhogadopsis pratellae(Weng & Chen, 2005) comb. n., Rhogadopsis pratensis (Weng & Chen, 2005) comb. n., Rhogadopsis sculpta (Chen & Weng, 2005) comb. n., Rhogadopsis sulcifer (Fischer, 1975) comb. n.,
Rhogadopsis tabidula(Weng & Chen, 2005) comb. n.,
Xynobius complexus (Weng & Chen, 2005) comb. n., Xynobius indagatrix (Weng & Chen, 2005) comb. n.,
Xynobius multiarculatus (Chen & Weng, 2005) comb. n.The following (sub)genera are synonymised: Snoflakopius Fischer, 1972, Jucundopius Fischer, 1984, Opiotenes Fischer, 1998, and Oetztalotenes Fischer, 1998, with Opiostomus Fischer, 1971; Xynobiotenes Fischer, 1998, with Xynobius Foerster, 1862; Allotypus Foerster, 1862, Lemnaphilopius Fischer, 1972, Agnopius Fischer, 1982, and Cryptognathopius Fischer, 1984, with Apodesmia Foerster, 1862; Nosopoea Foerster, 1862, Tolbia Cameron, 1907, Brachycentrus Szépligeti, 1907, Baeocentrum Schulz, 1911, Hexaulax Cameron, 1910, Coeloreuteus Roman, 1910, Neodiospilus Szépligeti, 1911, Euopius Fischer, 1967, Gerius Fischer, 1972, Grimnirus Fischer, 1972, Hoenirus Fischer, 1972, Mimirus Fischer, 1972, Gastrosema Fischer, 1972, Merotrachys Fischer, 1972, Phlebosema Fischer, 1972, Neoephedrus Samanta, Tamili, Saha & Raychaudhuri, 1983, Adontopius Fischer, 1984, Kainopaeopius Fischer, 1986, Millenniopius Fischer, 1996, and Neotropopius Fischer, 1999, with Phaedrotoma Foerster, 1862. 相似文献
20.
D. N. Kobakhidze 《BioControl》1965,10(4):323-330
Résumé Nous avons brièvement indiqué dans cette note les travaux de lutte biologique entrepris en Géorgie par introduction d'entomophages
parasites et prédateurs contre des Insectes nuisibles également introduits auparavant. Nous avons particulièrement souligné
l'importance deAphelinus mali
Muls. contreEriosoma lanigerum
Hausm.,Rodalia cardinalis
Muls. contreIcerya purchasi
Mask.,Cryptolaemus montrouzieri
Muls. contrePseudococcus gahani
Green,Lindorus lophanthae
Blaisdell contre une série de Diaspidides (Aspidiotus hederae
Vall.,A. destructor
Sign.,Chrysomphalus dictyospermi (Morg.),Aonidiella citrina
Coq.),Prospaltella berlesi
How. contrePseudaulacaspis pentagona
Targ.,Pseudaphycus malinus contrePseudococcus comstocki (Kuw.),Leptomastix dactylopii
How.
et Leptomastidea abnormis (Gyr.) contrePseudococcus vitis
Niet.,Rhizophagus grandis
Gyll. contreDendroctonus micans
Kugel.
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