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1.
Jere Kahanp?? 《ZooKeys》2014,(441):183-207
An updated checklist of the Atelestidae, Brachystomatidae, Dolichopodidae, Empididae and Hybotidae (Diptera) recorded from Finland is presented. The genera with uncertain placement within superfamily Empidoidea (= the Iteaphila group) are also included in this paper. 相似文献
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Jere Kahanp?? 《ZooKeys》2014,(441):291-303
A checklist of the Agromyzidae (Diptera) recorded from Finland is presented. 279 (or 280) species are currently known from the country. Phytomyza
linguae Lundqvist, 1947 is recorded as new to Finland. 相似文献
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A checklist of 112 species of shore flies (Ephydridae, Diptera) recorded from Finland is presented. Comparing this to the list of Hackman (1980), 52 changes are made: 25 species are added (all but one recorded after 1980), 18 misidentifications are deleted, 5 junior synonyms are replaced and 5 updated generic combinations are given. 相似文献
5.
Karnyothrips cyathomorphus
sp. n. (Phlaeothripidae: Phlaeothripinae) is described as a new apterous species in the genus Karnyothrips Watson 1923, and it represents the fourth species of the genus to be recorded from China. A key to the Chinese species is given. 相似文献
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In this study, the findings of three water mite species of the family Hygrobatidae collected from different streams in Turkey were evaluated. Hygrobates (s. str.) anatolicus Esen & Pešić, sp. n. is described as new for science. Hygrobates (Rivobates) diversiporus Sokolow, 1927 and Atractides (s. str.) nikooae Pešić, 2004, which were illustrated and thoroughly discussed, are new records for the Turkish fauna. 相似文献
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Fariba Mozaffarian 《ZooKeys》2013,(319):231-248
Iran is known as the most complex and varied country in southwest Asia, in terms of geography, vegetation, climate and consequently biological diversity. The rather high number of recorded endemic species of Fulgoromorpha in Iran indicates a high potential for speciation in some areas.In this study, in order to identify the endemic zones for Fulgoromorpha of Iran, three main biogeographic regions of the country were divided into 13 primary zones, mainly according to the distribution of published and unpublished locality records of endemic species. Using Venn diagrams and cluster analyses on the primary zones, 6 final endemic zones were recognized: Caspian zone, southern slopes of Alborz, Zagros Mountains, Kerman Mountains, Khorasan Mountains, and Baluchestan and Persian Gulf coasts. Then a similarity map was produced for endemic zones using a Multidimensional analysis (Alscal) and the differences between the positions of the same zones in the similarity and geographic maps were discussed. 相似文献
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The genus Planinasus Cresson is revised and includes 18 extant and one fossil species. We clarify the status of the three previously described species and describe 15 new species as follows (type locality in parenthesis): Planinasus aenigmaticus (Colombia. Bogota: Bogota (04°35.8''N, 74°08.8''W)), Planinasus neotropicus (Panama. Canal Zone: Barro Colorado Island (09°09.1''N, 79°50.8''W)), Planinasus kotrbae (Ecuador. Orellana: Rio Tiputini Biodiversity Station (0°38.2''S, 76°08.9''W)), Planinasus miradorus (Brazil. Maranhão: Parque Estadual Mirador, Base da Geraldina (06°22.2''S, 44°21.8''W)), Planinasus tobagoensis (Trinidad and Tobago. Tobago. St. John: Parlatuvier (11°17.9''N, 60°39''W)), Planinasus xanthops (Ecuador. Orellana: Rio Tiputini Biodiversity Station (0°38.2''S, 76°8.9''W)), Planinasus argentifacies (Peru. Madre de Dios: Río Manu, Pakitza (11°56.6''S, 71°16.9''W; 250 m)), Planinasus insulanus (Dominican Republic. La Vega: near Jarabacoa, Salto Guasara (19°04.4''N, 70°42.1''W, 680 m)), Planinasus nigritarsus (Guyana. Conservation of Ecological Interactions and Biotic Associations (CEIBA; ca. 40 km S Georgetown; 06°29.9''N, 58°13.1''W)), Planinasus atriclypeus (Brazil. Rio de Janeiro: Rio de Janeiro, Floresta da Tijuca (22°57.6''S, 43°16.4''W)), Planinasus atrifrons (Bolivia. Santa Cruz: Ichilo, Buena Vista (4-6 km SSE; Hotel Flora y Fauna; 17°29.95''S, 63°33.15''W; 4-500 m)), P. flavicoxalis (West Indies. Dominica. St. David: 1.6 km N of junction of roads to Rosalie and Castle Bruce (15°23.8''N, 61°18.6''W)), Planinasus mcalpineorum (Mexico. Chiapas: Cacahoatan (7 km N; 15°04.1''N, 92°07.4''W)), Planinasus nigrifacies (Brazil. São Paulo: Mogi das Cruzes, Serra do Itapeti (23°31.5''S, 46°11.2''W)), Planinasus obscuripennis (Peru. Madre de Dios: Río Manu, Erika (near Salvación; 12°50.7''S, 71°23.3''W; 550 m)). In addition to external characters, we also describe and illustrate structures of the male terminalia and for Planinasus kotrbae
sp. n., the internal female reproductive organs. Detailed locality data and distribution maps for all species are provided. For perspective and to facilitate genus-group and species-group recognition, the family Periscelididae and subfamily Stenomicrinae are diagnosed and for the latter, a key to included genera is provided. 相似文献
11.
Three new species of the streptaxid snail genus Perrottetia are described from north and northeastern Thailand, Perrottetia aquilonaria
sp. n., Perrottetia dermapyrrhosa
sp. n. and Perrottetia phuphamanensis
sp. n. Each species is endemic to a single or a few limestone mountain ranges. The species are characterized by the morphology of their genital organs, as well as by shell characters. Perrottetia aquilonaria
sp. n. has a club shaped distal penis and large penial hooks are present and penial papillae cover almost the entire penial hook portion; adjacent areas possess low reticulated folds. Perrottetia dermapyrrhosa
sp. n. has a long genital atrium and the penial sheath is about two-thirds of the penis length. Penial hooks are long, scattered and sunken into deep ovate hollows; vaginal hooks are present. Perrottetia phuphamanensis sp. n. has a rounded and protruded shell periphery. The aperture is subcircular, peristome is thick and the second parietal lamella is adjacent to the first parietal lamella; a basal lamella is the smaller than in the other Thai species. 相似文献
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Two new species are added to the rare pompilid genus Abernessia Arlé. Abernessia capixaba
sp. n. and A. giga
sp. n. are described and illustrated. This is the first record of the genus from the states of Espírito Santo and Minas Gerais, Brazil. The genus now contains four species. A brief discussion of generic characters, illustrations, and a key to the known species of Abernessia are provided. 相似文献
13.
Adenomar Neves de Carvalho 《ZooKeys》2012,(242):19-24
Paraportanus longispinus,, a new leafhopper species from Roraima and Amazonas States, North Brazil, is described and illustrated. The new species can be recognized by the male genital features, especially the distal third of ventral margin of the pygofer with a dentiform short process; plates distinctly longer than pygofer, extending posteriorly beyond pygofer by approximately 1/3 of their length and aedeagus with one pair of spiniform process long crossed and directed ventrally. A checklist and key to males of all known Paraportanus species is provided. 相似文献
14.
The pupal stage of eleven Opatrini species occuring in the northern China are described and a key for their identifiaction is provided. The species are Scleropatrum horridum horridum Reitter, Gonocephalum reticulatum Motschulsky, Opatrum (Opatrum) subaratum Faldermann, Eumylada potanini (Reitter), Eumylada punctifera (Reitter), Penthicus (Myladion) alashanicus (Reichardt), Penthicus (Myladion) nojonicus (Kaszab), Myladina unguiculina Reitter, Melanesthes (Opatronesthes) rugipennis Reitter, Melanesthes (Melanesthes) maxima maxima Ménétriès and Melanesthes (Melanesthes) jintaiensis Ren. 相似文献
15.
Three new species of the Oriental empoascine leafhopper genus Dayus Mahmood are described from China: D. bifurcatus
sp. n., D. trifurcatus
sp. n. and D. serratus
sp. n. A key to distinguish all Chinese species of the genus is provided. 相似文献
16.
Here we present a complete revision of the species of Baconia. Up until now there have been 27 species assigned to the genus (Mazur, 2011), in two subgenera (Binhister Cooman and Baconia s. str.), with species in the Neotropical, Nearctic, Palaearctic, and Oriental regions. We recognize all these species as valid and correctly assigned to the genus, and redescribe all of them. We synonymize Binhister, previously used for a polyphyletic assemblage of species with varied relationships in the genus. We move four species into Baconia from other genera, and describe 85 species as new, bringing the total for the genus to 116 species. We divide these into 12 informal species groups, leaving 13 species unplaced to group. We present keys and diagnoses for all species, as well as habitus photos and illustrations of male genitalia for nearly all. The genus now contains the following species and species groups: Baconia loricata group [Baconia loricata Lewis, 1885, B. patula Lewis, 1885, Baconia gounellei (Marseul, 1887a), Baconia jubaris (Lewis, 1901), Baconia festiva (Lewis, 1891), Baconia foliosoma
sp. n., Baconia sapphirina
sp. n., Baconia furtiva
sp. n., Baconia pernix
sp. n., Baconia applanatis
sp. n., Baconia disciformis
sp. n., Baconia nebulosa
sp. n., Baconia brunnea
sp. n.], Baconia godmani group [Baconia godmani (Lewis, 1888), Baconia venusta (J. E. LeConte, 1845), Baconia riehli (Marseul, 1862), comb. n., Baconia scintillans
sp. n., Baconia isthmia
sp. n., Baconia rossi
sp. n., Baconia navarretei
sp. n., Baconia maculata
sp. n., Baconia deliberata
sp. n., Baconia excelsa
sp. n., Baconia violacea (Marseul, 1853), Baconia varicolor (Marseul, 1887b), Baconia dives (Marseul, 1862), Baconia eximia (Lewis, 1888), Baconia splendida
sp. n., Baconia jacinta
sp. n., Baconia prasina
sp. n., Baconia opulenta
sp. n., Baconia illustris (Lewis, 1900), Baconia choaspites (Lewis, 1901), Baconia lewisi Mazur, 1984], Baconia salobrus group [Baconia salobrus (Marseul, 1887b), Baconia turgifrons
sp. n., Baconia crassa
sp. n., Baconia anthracina
sp. n., Baconia emarginata
sp. n., Baconia obsoleta
sp. n.], Baconia ruficauda group [Baconia ruficauda
sp. n., Baconia repens
sp. n.], Baconia angusta group [Baconia angusta Schmidt, 1893a, Baconia incognita
sp. n., Baconia guartela
sp. n., Baconia bullifrons
sp. n., Baconia cavei
sp. n., Baconia subtilis
sp. n., Baconia dentipes
sp. n., Baconia rubripennis
sp. n., Baconia lunatifrons
sp. n.], Baconia aeneomicans group [Baconia aeneomicans (Horn, 1873), Baconia pulchella
sp. n., Baconia quercea
sp. n., Baconia stephani
sp. n., Baconia irinae
sp. n., Baconia fornix
sp. n., Baconia slipinskii Mazur, 1981, Baconia submetallica
sp. n., Baconia diminua
sp. n., Baconia rufescens
sp. n., Baconia punctiventer
sp. n., Baconia aulaea
sp. n., Baconia mustax
sp. n., Baconia plebeia
sp. n., Baconia castanea
sp. n., Baconia lescheni
sp. n., Baconia oblonga
sp. n., Baconia animata
sp. n., Baconia teredina
sp. n., Baconia chujoi (Cooman, 1941), Baconia barbarus (Cooman, 1934), Baconia reposita
sp. n., Baconia kubani
sp. n., Baconia wallacea
sp. n., Baconia bigemina
sp. n., Baconia adebratti
sp. n., Baconia silvestris
sp. n.], Baconia cylindrica group [Baconia cylindrica
sp. n., Baconia chatzimanolisi
sp. n.], Baconia gibbifer group [Baconia gibbifer
sp. n., B. piluliformis
sp. n., Baconia maquipucunae
sp. n., Baconia tenuipes
sp. n., Baconia tuberculifer
sp. n., Baconia globosa
sp. n.], Baconia insolita group [Baconia insolita (Schmidt, 1893a), comb. n., Baconia burmeisteri (Marseul, 1870), Baconia tricolor
sp. n., Baconia pilicauda
sp. n.], Baconia riouka group [Baconia riouka (Marseul, 1861), Baconia azuripennis
sp. n.], Baconia famelica group [Baconia famelica
sp. n., Baconia grossii
sp. n., Baconia redemptor
sp. n., Baconia fortis
sp. n., Baconia longipes
sp. n., Baconia katieae
sp. n., Baconia cavifrons (Lewis, 1893), comb. n., Baconia haeterioides
sp. n.], Baconia micans group [Baconia micans (Schmidt, 1889a), Baconia carinifrons
sp. n., Baconia fulgida (Schmidt, 1889c)], Baconia incertae sedis [Baconia chilense (Redtenbacher, 1867), Baconia glauca (Marseul, 1884), Baconia coerulea (Bickhardt, 1917), Baconia angulifrons
sp. n., Baconia sanguinea
sp. n., Baconia viridimicans (Schmidt, 1893b), Baconia nayarita
sp. n., Baconia viridis
sp. n., Baconia purpurata
sp. n., Baconia aenea
sp. n., Baconia clemens
sp. n., Baconia leivasi
sp. n., Baconia atricolor
sp. n.]. We designate lectotypes for the following species: Baconia loricata Lewis, 1885,Phelister gounellei Marseul, 1887, Baconia jubaris Lewis, 1901, Baconia festiva Lewis, 1891, Platysoma venustum J.E. LeConte, 1845, Phelister riehli Marseul, 1862, Phelister violaceus Marseul, 1853, Phelister varicolor Marseul, 1887b, Phelister illustris Lewis, 1900, Baconia choaspites Lewis, 1901, Epierus festivus Lewis, 1898, Phelister salobrus Marseul, 1887, Baconia angusta Schmidt, 1893a, Phelister insolitus Schmidt, 1893a, Pachycraerus burmeisteri Marseul, 1870, Phelister riouka Marseul, 1861, Homalopygus cavifrons Lewis, 1893, Phelister micans Schmidt, 1889a, Phelister coeruleus Bickhardt, 1917, and Phelister viridimicans Schmidt, 1893b. We designate neotypes for Baconia patula Lewis, 1885 and Hister aeneomicans Horn, 1873, whose type specimens are lost. 相似文献
17.
One new species, Schwarzerium yunnanum
sp. n. is described from Yunnan Province, China. And a new subgenus Rugosochroma
subgen. n. is erected for it. Additionally, Seven species of the tribe Callichromatini are newly recorded from China: Aphrodisium niisatoi Vives & Bentanachs, 2007, Aphrodisium tricoloripes Pic, 1925, Chelidonium violaceimembris Gressitt & Rondon, 1970 (new from Vietnam too), Chloridolum grossepunctatum Gressitt & Rondon, 1970 (new from Vietnam too), Chloridolum semipunctatum Gressit & Rondon 1970, Embrikstrandia vivesi Bentanachs, 2005 and Laosaphrodisium subplicatum (Pic, 1937). 相似文献
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Karin Breugelmans Kurt Jordaens Els Adriaens Jean Paul Remon Josep?Quintana Cardona Thierry Backeljau 《ZooKeys》2013,(365):83-104
The Iberian Peninsula is a region with a high endemicity of species of the terrestrial slug subgenus Mesarion. Many of these species have been described mainly on subtle differences in their proximal genitalia. It therefore remains to be investigated 1) whether these locally diverged taxa also represent different species under a phylogenetic species concept as has been shown for other Mesarion species outside the Iberian Peninsula, and 2) how these taxa are phylogenetically related. Here, we analysed DNA sequence data of two mitochondrial (COI and 16S) genes, and of the nuclear ITS1 region, to explore the phylogenetic affinities of two of these endemic taxa, viz. Arion gilvus Torres Mínguez, 1925 and A. ponsi Quintana Cardona, 2007. We also evaluated the use of these DNA sequence data as DNA barcodes for both species. Our results showed that ITS did not allow to differentiate among most of the Mesarion molecular operational taxonomic units (MOTUs) / morphospecies in Mesarion. Yet, the overall mean p-distance among the Mesarion MOTUs / morphospecies for both mtDNA fragments (16.7% for COI, 13% for 16S) was comparable to that between A. ponsi and its closest relative A. molinae (COI: 14.2%; 16S: 16.2%) and to that between A. gilvus and its closest relative A. urbiae (COI: 14.4%; 16S: 13.4%). Hence, with respect to mtDNA divergence, both A. ponsi and A. gilvus, behave as other Mesarion species or putative species-level MOTUs and thus are confirmed as distinct ‘species’. 相似文献
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Tangius indicus
sp. n. (Batrisitae: Batrisini) is described and illustrated from the Indian States of Meghalaya (Khasi Hills, type locality) and West Bengal (Darjeeling). Specimens of the new species are similar to those of the recently described T. glabellus Yin & Li from Tibet, Southwest China, and can be separated only by minor differences of the male features. 相似文献