scholarly journals Two new species of the genus Scathophaga (Diptera: Scathophagidae) from Svalbard, with a key to selected northern species and comments on their taxonomy

Author(s):  
František Šifner

Abstract Two new Palaearctic species, Scathophaga annae sp. nov. and Scathophaga simaceki sp. nov. are described from Svalbard. An illustrated identification key for selected northern species from of the genus Scathophaga from the Palaearctic and Nearctic Regions is given. Two new combinations are provided: Coniostenum molle (Becker, 1894) comb.nov. for Scathophaga mollis (Becker, 1894) and Coniosternum nigripalpis (Becker, 1907) comb. nov. for Scathophaga nigripalpis (Becker, 1907). Two new synonyms are established, Scathophaga (Coniosternum) sychevskaye Ozerov, 2010, syn. nov. = Coniosternum molle and Scathophaga minuta (Maloch, 1935), syn. nov. = Coniosterum lapponicum Ringdahl, 1920. Scathophaga islandica (Becker, 1894) and Scathophaga villipes (Zetterstedt, 1846) are confirmed as valid species. The species Scathophaga furcata (Say, 1823) is confirmed again in this area. Scathophaga janmayeni (Séguy, 1939) is species incertae sedis. Scathophaga islandica (Becker, 1894) is first recorded from Greenland and Sweden (Lappland).

Zootaxa ◽  
2009 ◽  
Vol 2104 (1) ◽  
pp. 1-76 ◽  
Author(s):  
RUTH BARNICH ◽  
DIETER FIEGE

The type material and original descriptions of 126 nominal species from the Northeast Atlantic originally described as belonging to Harmothoe Kinberg, 1856 or later referred to this genus were examined. Of these species, only 28 are considered to be valid, i.e. less than 25 %, the others being either junior synonyms, indeterminable, invalid, or referred to other genera. The valid species are described and figured, including two new species, H. fernandi n. sp. and H. mariannae n. sp. For H. extenuata (Grube, 1840), H. imbricata (Linnaeus, 1767), and H. impar (Johnston, 1839), neotypes are designated, since their type material is lost and their original descriptions are insufficient. Harmothoe aequespina (Langerhans, 1884) and H. clavigera (M. Sars, 1863) represent new combinations. An illustrated identification key to all valid Harmothoe species of the region is given.


Phytotaxa ◽  
2015 ◽  
Vol 239 (1) ◽  
pp. 1 ◽  
Author(s):  
Raquel Stauffer Viveros ◽  
Alexandre Salino

Two new species of Ctenitis (Dryopteridaceae) from South America are described and illustrated: Ctenitis christensenii is endemic to southeastern Brazil and C. glandulosa occurs from southeastern to northeastern Brazil and in Guyana. An identification key and notes about the distribution, habitat and taxonomy of the new species, C. falciculata and allies are provided. Moreover, seven lectotypifications and two new synonyms are proposed.


Zootaxa ◽  
2019 ◽  
Vol 4677 (1) ◽  
pp. 1-68 ◽  
Author(s):  
OLEKSIY BIDZILYA ◽  
OLE KARSHOLT ◽  
VASILIY KRAVCHENKO ◽  
JAN ŠUMPICH

One hundred forty-six species of Gelechiidae including 36 new records are reported from Israel. Anarsia balioneura Meyrick, 1921 and Polyhymno chionarcha Meyrick, 1913 are recorded for the first time in the Palaearctic region. Two new species are described: Metzneria freidbergi sp. nov., and Scrobipalpa aravensis sp. nov. Six new synonyms are established: Stygmatoptera Hartig, 1936 syn. nov. of Polyhymno Chambers, 1874; Eulamprotes Bradley, 1971 syn. nov. of Oxypteryx Rebel, 1911; Polyhymno abaiella Amsel, 1974 syn. nov. of Polyhymno chionarcha, Meyrick, 1913; Gelechia haifella Amsel, 1935 syn. nov. of Athrips rancidella (Herrich-Schäffer, 1854); Sophronia catharurga Meyrick, 1923 and Sophronia parahumerella Amsel, 1935 syn. nov. of Pseudosophronia exustellus (Zeller, 1847). The following new combinations are proposed: Anacampsis karmeliella (Amsel, 1935) comb. nov., Stomopteryx tesserapunctella (Amsel, 1935) comb. nov., Aproaerema languidella (Amsel, 1936) comb. nov., Aproaerema telaviviella (Amsel, 1935) comb. nov., Acompsia (Telephila) ballotellus (Amsel, 1935) comb. nov., Polyhymno dumonti (Hartig, 1936) comb. nov., Oxypteryx atrella (Denis & Schiffermüller, 1775) comb. nov., Oxypteryx immaculatella (Douglas, 1850) comb. nov. and Chrysoesthia amseli (Bidzilya, 2008) comb. nov. A lectotype is designated for Lita rhamnifoliae Amsel & Hering, 1931.The genitalia of both sexes of Sophronia sagittans Meyrick, 1923, Anacampsis karmeliella (Amsel, 1935), Stomopteryx tesserapunctella Amsel, 1935 as well as male genitalia of Stomopteryx lacteolella Caradja, 1924, Aproaerema telaviviella (Amsel, 1935), Acompsia ballotellus (Amsel, 1935), Polyhymno dumonti (Hartig, 1936) and Chrysoesthia amseli (Bidzilya, 2008) are illustrated and described for the first time. New or additional host plants are recorded for Metzneria aspretella Lederer, 1869, M. agraphella (Ragonot, 1895), M. ehikeella Gozmány, 1954 and Scrobipalpa suaedivorella (Chrétien, 1915). Photographs of the type specimens of most taxa described from Israel and Palestine are presented. The following species are removed from the list of Gelechiidae of Israel: Nothris sulcella Staudinger, 1879, N. skyvai Karsholt & Šumpich, 2015, Anarsia spartiella Schrank, 1802, Megacraspedus cerussatellus Rebel, 1930, Oxypteryx atrella (Denis & Schiffermüller, 1775), Isophrictis anthemidella (Wocke, 1871), Metzneria metzneriella (Stainton, 1851), Scrobipalpa otregata Povolný, 1972, Scrobipalpa nitentella (Fuchs, 1902), Scrobipalpa remota Povolný, 1972, Scrobipalpa salinella (Zeller, 1847) and Ephysteris diminutella (Zeller, 1847). Moreover, Stomopteryx remissella (Zeller, 1847) is recorded as new to the Altai Mountains of Russia, Anarsia balioneura Meyrick, 1921 is new to Cyprus and Libya, Polyhymno dumonti (Hartig, 1936) is new to Libya and Sudan, Scrobipalpa superstes is new to Greece, Stenolechia gemmella (Linnaeus, 1758) is new to Jordan and Polyhymno chionarcha is new to Saudi Arabia. 


Zootaxa ◽  
2020 ◽  
Vol 4858 (1) ◽  
pp. 111-125
Author(s):  
OLEG P. NEGROBOV ◽  
STEFAN NAGLIS

Thrypticus caeruleus Naglis & Negrobov sp. nov. and T. kechevi Naglis & Negrobov sp. nov. are newly described from Turkey. Thrypticus viridis Parent is redescribed and the hypopygium is figured in detail. A revised checklist and key to males of Palaearctic species of the genus Thrypticus Gerstäcker including 26 valid species are provided. Thrypticus paludicola Negrobov is restored from synonymy with T. intercedens Negrobov based on hypopygial differences. Thrypticus tonsus Negrobov is regarded as new synonym of T. subtilis Negrobov. 


2019 ◽  
Vol 7 ◽  
Author(s):  
AJ Fleming ◽  
D. Monty Wood ◽  
M. Alex Smith ◽  
Tanya Dapkey ◽  
Winnie Hallwachs ◽  
...  

We describe 22 new species in the genus Hyphantrophaga Townsend, 1892 (Diptera: Tachinidae) from Area de Conservación Guanacaste (ACG) in north-western Costa Rica. All species were reared from an ongoing inventory of wild-caught caterpillars spanning a variety of families (Lepidoptera: Bombycidae, Crambidae, Depressariidae, Doidae, Erebidae, Euteliidae, Gelechiidae, Geometridae, Hedylidae, Hesperiidae, Immidae, Lasiocampidae, Limacodidae, Megalopygidae, Mimaloniidae, Noctuidae, Nolidae, Notodontidae, Nymphalidae, Papilionidae, Pieridae, Phiditiidae, Pterophoridae, Pyralidae, Riodinidae, Saturniidae, Sphingidae, Thyrididae, Tortricidae and Zygaenidae). We provide a morphological description of each species together with information on life history, molecular data and photographic documentation. In addition to the new species, we provide a redescription of the genus, as well as the redescription of three previously described species, which were also collected within ACG during this study: Hyphantrophagaangustata (van der Wulp), Hyphantrophagamyersi (Aldrich) and Hyphantrophagavirilis (Aldrich & Webber). The following 22 new species of Hyphantrophaga are described: Hyphantrophagaadrianguadamuzi Fleming & Wood sp. n., Hyphantrophagaalbopilosa Fleming & Wood sp. n., Hyphantrophagaanacordobae Fleming & Wood sp. n., Hyphantrophagacalixtomoragai Fleming & Wood sp. n., Hyphantrophagacalva Fleming & Wood sp. n.., Hyphantrophagaciriloumanai Fleming & Wood sp. n., Hyphantrophagadanausophaga Fleming & Wood sp. n., Hyphantrophagadiniamartinezae Fleming & Wood sp. n., Hyphantrophagaduniagarciae Fleming & Wood sp. n., Hyphantrophagaedwinapui Fleming & Wood sp. n., Hyphantrophagaeldaarayae Fleming & Wood sp. n., Hyphantrophagaeliethcantillanoe Fleming & Wood sp. n., Hyphantrophagagilberthampiei Fleming & Wood sp. n., Hyphantrophagaguillermopereirai Fleming & Wood sp. n., Hyphantrophagahazelcambroneroae Fleming & Wood sp. n., Hyphantrophagaluciariosae Fleming & Wood sp. n., Hyphantrophagamanuelriosi Fleming & Wood sp. n., Hyphantrophagamorphophaga Fleming & Wood sp. n., Hyphantrophaganigricauda Fleming & Wood sp. n., Hyphantrophagaosvaldoespinozai Fleming & Wood sp. n., Hyphantrophagapabloumanai Fleming & Wood sp. n. and Hyphantrophagasimilis Fleming & Wood sp. n. The following are proposed by Wood as new synonyms of Hyphantrophaga Townsend, 1892: Brachymasicera Townsend, 1911 syn. n., Ommasicera Townsend, 1911 syn. n., Ophirosturmia Townsend, 1911 syn. n., Patillalia Curran, 1934 syn. n. and Ypophaemyiops Townsend, 1935 syn. n. The following nine new combinations are proposed as a result of the new synonymies: Hyphantrophagaadamsoni (Thompson, 1963), comb. n., Hyphantrophagafasciata (Curran, 1934), comb. n., Hyphantrophagaglauca (Giglio-Tos, 1893), comb. n., Hyphantrophagagowdeyi (Curran, 1926), comb. n., Hyphantrophagamyersi (Aldrich, 1933), comb. n., Hyphantrophaganigripes (Townsend, 1928), comb. n., Hyphantrophagaoptica (Schiner, 1868), comb. n., Hyphantrophagapolita (Townsend, 1911), comb. n., Hyphantrophagasubpolita (Townsend, 1912), comb. n.


2019 ◽  
Vol 50 (2) ◽  
pp. 235-296 ◽  
Author(s):  
Mar Ferrer-Suay ◽  
Jesús Selfa ◽  
Noel Mata-Casanova ◽  
Nicolas Pérez Hidalgo ◽  
Juli Pujade-Villar

A complete revision of the world species of the genus Phaenoglyphis Förster, 1869 has been conducted. A total of 25 species of Phaenoglyphis are valid after studying their type material. Two new species are described: Phaenoglyphis belizini sp. n. and Phaenoglyphis palmirae sp. n. Two species are synonymized: P. dolichocera (Cameron, 1889) with P. nigripes (Thomson, 1877) and P. pecki Andrews, 1978 with P. villosa (Hartig, 1841). Phaenoglyphis bangalorensis Kurian, 1953 was considered as incertae sedis. Phaenoglyphis duplocarpentieri (Kieffer, 1904) and P. hedickei Hedicke, 1928 are considered lost. Other three species are discarded as valid species because they are missing important parts without which the species cannot be defined: P. cincta (Hartig, 1841), P. frigidus (Belizin, 1968) and P. repentinus Belizin, 1962. A complete redescription and an illustrative plate are presented. A key to species of the genus Phaenoglyphis is given. Phylogenetic analysis based on morphological characters has been performed.


Zootaxa ◽  
2020 ◽  
Vol 4729 (4) ◽  
pp. 482-500
Author(s):  
KOBRA HASHEMI ◽  
AKBAR KAREGAR

During a survey conducted during 2013–2017, five known and two new species of Nothotylenchus Thorne, 1941 were collected from the southern provinces of Iran. N. brzeskii n. sp. is characterised by a body length of 774–922 µm, lateral fields with four incisures, delicate, short stylet (7–8 µm) with small rounded knobs, pyriform, offset or slightly overlapping basal pharyngeal bulb, posterior vulva position (V = 83.4–84.4), short PUS (5–10 µm), spicules 20.5–23 µm long, and thick tail with rounded to dull terminus. N. siddiqi n. sp. is characterised by a body length of 573–645 µm, six to nine incisures in lateral fields, delicate, short stylet (6.5–7.5 µm) with rounded knobs, pyriform or slightly elongate and offset basal pharyngeal bulb, V = 79.3–81.0, PUS = 26.5–40 µm, short spicules = 14.5–16.5 µm, and tail with rounded terminus. Morphometric data of the studied species are presented and intraspecific variation of their morphometrics and morphological characters is discussed. The list of world Nothotylenchus species is updated, and a dichotomous identification key and an updated tabular compendium for 41 valid species are provided. 


Zootaxa ◽  
2017 ◽  
Vol 4227 (4) ◽  
pp. 563 ◽  
Author(s):  
BEHNAM MOTAMEDINIA ◽  
CHRISTIAN KEHLMAIER ◽  
AZIZOLLAH MOKHTARI ◽  
EHSAN RAKHSHANI ◽  
EBRAHIM GILASIAN

The genus Claraeola Aczél is recorded from Iran for the first time. Two new species, Claraeola parnianae Motamedinia & Kehlmaier sp. nov. and Claraeola khorshidae Motamedinia & Kehlmaier sp. nov., are described and illustrated. An updated identification key to the Western Palaearctic species of the genus Claraeola is provided. Both species were characterized morphologically and by DNA barcoding of the mitochondrial COI gene. 


Zootaxa ◽  
2013 ◽  
Vol 3606 (1) ◽  
pp. 1-110 ◽  
Author(s):  
P. ROS-FARRÉ ◽  
J. PUJADE-VILLAR

The genus Aspicera Dahlbom (Hymenoptera: Cynipoidea: Figitidae: Aspicerinae) is revised herein. Aspicera has a Holarctic distribution, being here cited for the first time from the following countries: Canada, Cyprus, Greece, India (northeastern corner, which is part of the Himalayan southeastern range and is considered as belonging to the Palaearctic), Japan, Jordan, Mexico, Montenegro, and Turkey. Morphological characters necessary to differentiate the species of Aspicera are described. The 27 previously described species of Aspicera were revised, always studying the type material when available (21 species); the type material of A. aegyptica Hedicke, 1928, A. chlapowskii Kieffer, 1901, A. coriacea Kieffer, 1901, A. lobata Hedicke, 1928, A. sibirica Kieffer, 1901, A. spinosa (Boyer de Fonscolombe, 1832) are lost or destroyed, these species were studied with the original descriptions. Of the 27 known species, 16 are considered as valid and are redescribed; A. effincta Belizin, 1952 is syn. nov. of A. suecica Dalla Torre & Kieffer, 1910, and A. brevispina Kieffer, 1901 and A. coriacia Kieffer, 1901 are syn. nov. of A. hartigi Dalla Torre, 1889. Aspicera nigra Ionescu, 1969, A. nigricornis Kirby, 1889 and A. rugosa (Hartig, 1843) do not belong to the Aspicerinae, but respectively to the genera Xyalophora and Neralsia (Figitinae), and Xyalaspis (Anacharitinae): Xyalophora nigra (Ionescu) n. comb., Neralsia nigricornis (Kirby) n. comb. and Xyalaspis rugosa Hartig status restored. Aspicera lobata Hedicke, 1928 is considered as ‘incertae sedis’. The examination of additional specimens suggests that there is a general lack of knowledge of the species diversity of this genus. Thirty two new species are described: A. adelae Ros-Farré n. sp., A. annae Ros-Farré & Pujade-Villar n. sp., A. belizini Ros-Farré & Pujade-Villar n. sp., A. blancae Ros-Farré n. sp., A. buffingtoni Ros-Farré & Pujade-Villar n. sp., A. caminali Ros-Farré n. sp., A. carinata Ros-Farré & Pujade-Villar n. sp., A. dianae Ros-Farré n. sp., A. kovalevi Ros-Farré & Pujade-Villar n. sp., A. elisendae Ros-Farré n. sp., A. forshzarai Pujade-Villar & Ros-Farré n. sp., A. gemmae Ros-Farré & Pujade-Villar n. sp., A. jantonii Ros-Farré n. sp., A. julii Ros-Farré & Pujade-Villar n. sp., A. kiefferi Ros-Farré & Pujade-Villar n. sp., A. magdae Ros-Farré & Pujade-Villar n. sp., A. marginata Ros-Farré & Pujade-Villar n. sp., A. martae Ros-Farré & Pujade-Villar n. sp., A. danielssoni Ros-Farré & Pujade-Villar n. sp., A. carlestolrai Ros-Farré & Pujade-Villar n. sp., A. mireiae Ros-Farré & Pujade-Villar n. sp., A. porif Ros-Farré n. sp., A. marginata Ros-Farré & Pujade-Villar n. sp., A. punctifrons Ros-Farré & Pujade-Villar n. sp., A. readae Ros-Farré & Pujade-Villar n. sp., A. robusta Ros-Farré & Pujade-Villar n. sp., A. santamariai Ros-Farré & Pujade-Villar n. sp., A. sergioi Ros-Farré n. sp., A. singularica Ros-Farré & Pujade-Villar n. sp., A. teresae Ros-Farré n. sp., A. tomasi Ros-Farré n. sp., A. zuparcoi Ros-Farré & Pujade-Villar n. sp. A key to all 48 valid species of Aspicera is given. All species are illustrated.


Author(s):  
Jan Bezděk

The genus Liroetis Weise, 1889 is redefi ned. The following new synonymies are established: Liroetis Weise, 1889 = Siemssenius Weise, 1922, syn. nov. = Pseudoliroetis Laboissière, 1929, syn. nov. = Zangia Chen, 1976, syn. nov. Consequently, the following new combinations are proposed: Liroetis coeruleus (Jiang, 1990) comb. nov.; Liroetis latispinus (Chen, 1976) comb. nov.; Liroetis nigricollis (Jiang, 1990) comb. nov.; Liroetis pallidulus (Jiang, 1990) comb. nov. (all from Zangia); Liroetis nigropictus (Fairmaire, 1889) comb. nov. (from Leptarthra); Liroetis cheni (Lee, 2016) comb. nov.; Liroetis elongatus (Kimoto, 1977) comb. nov.; Liroetis jeanvoinei (Laboissière, 1929) comb. nov.; Liroetis jungchani (Lee, 2016) comb. nov.; Liroetis liui (Lee, 2016) comb. nov.; Liroetis metallipennis (Chûjô, 1962) comb. nov.; Liroetis modestus (Weise, 1922) comb. nov.; Liroetis nigriceps (Laboissière, 1929) comb. nov.; Liroetis rufi pennis (Chûjô, 1962) comb. nov.; Liroetis sulcipennis (Zhang & Yang, 2008) comb. nov.; Liroetis tsoui (Lee, 2016) comb. nov.; and Liroetis yuae (Lee, 2016) comb. nov. (all from Siemssenius). Two new species, Liroetis aurantiacus sp. nov., from continental South East Asia, and L. baolocanus sp. nov., from Vietnam, are described. A new substitute name, Liroetis medvedevi nom. nov., is proposed for L. nigricollis Medvedev, 2009 preoccupied by L. nigricollis (Jiang, 1990). The following new synonyms are established: Liroetis aeneipennis Weise, 1889 = L. tiemushannis Jiang, 1988, syn. nov.; Liroetis ephippiatus Laboissière, 1930 = Zangia signata Jiang, 1990, syn. nov. = L. postmaculatus Lopatin, 2004, syn. nov.; Liroetis leechi Jacoby, 1890 = L. verticalis Jiang, 1988, syn. nov.; Liroetis nigricollis (Jiang, 1990) = L. unicolor Zhang, Li & Yang, 2008, syn. nov.; Liroetis reitteri (Pic, 1934) = Pseudoliroetis trifasciata Jiang, 1992, syn. nov. The spelling of Liroetis tiemushannis Jiang, 1988 is fixed using the First Reviewer Principle. Species of Liroetis are divided into five species-groups based on the combination of the following characters: presence/absence of border on anterior pronotal margin, width/length ratio of pronotum, structure of aedeagus, presence/absence of metatibial spur. The established groups are: the aeneipennis group, the aurantiacus group, the flavipennis group, the fulvipennis group, and the grandis group. The gender of Liroetis is masculine.


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