A new species of Hemibrycon (Characiformes,Characidae) from the upper San Juan River drainage,Pacific versant,Colombia

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).     

Taxonomic revision of the tarantula genus Aphonopelma Pocock, 1901 (Araneae,Mygalomorphae, Theraphosidae) within the United States

This systematic study documents the taxonomy, diversity, and distribution of the tarantula spider genus Aphonopelma Pocock, 1901 within the United States. By employing phylogenomic, morphological, and geospatial data, we evaluated all 55 nominal species in the United States to examine the evolutionary history of Aphonopelma and the group’s taxonomy by implementing an integrative approach to species delimitation. Based on our analyses, we now recognize only 29 distinct species in the United States. We propose 33 new synonymies (Aphonopelma apacheum, Aphonopelma minchi, Aphonopelma rothi, Aphonopelma schmidti, Aphonopelma stahnkei = Aphonopelma chalcodes; Aphonopelma arnoldi = Aphonopelma armada; Aphonopelma behlei, Aphonopelma vogelae = Aphonopelma marxi; Aphonopelma breenei = Aphonopelma anax; Aphonopelma chambersi, Aphonopelma clarum, Aphonopelma cryptethum, Aphonopelma sandersoni, Aphonopelma sullivani = Aphonopelma eutylenum; Aphonopelma clarki, Aphonopelma coloradanum, Aphonopelma echinum, Aphonopelma gurleyi, Aphonopelma harlingenum, Aphonopelma odelli, Aphonopelma waconum, Aphonopelma wichitanum = Aphonopelma hentzi; Aphonopelma heterops = Aphonopelma moderatum; Aphonopelma jungi, Aphonopelma punzoi = Aphonopelma vorhiesi; Aphonopelma brunnius, Aphonopelma chamberlini, Aphonopelma iviei, Aphonopelma lithodomum, Aphonopelma smithi, Aphonopelma zionis = Aphonopelma iodius; Aphonopelma phanum, Aphonopelma reversum = Aphonopelma steindachneri), 14 new species (Aphonopelma atomicum sp. n., Aphonopelma catalina sp. n., Aphonopelma chiricahua sp. n., Aphonopelma icenoglei sp. n., Aphonopelma johnnycashi sp. n., Aphonopelma madera sp. n., Aphonopelma mareki sp. n., Aphonopelma moellendorfi sp. n., Aphonopelma parvum sp. n., Aphonopelma peloncillo sp. n., Aphonopelma prenticei sp. n., Aphonopelma saguaro sp. n., Aphonopelma superstitionense sp. n., and Aphonopelma xwalxwal sp. n.), and seven nomina dubia (Aphonopelma baergi, Aphonopelma cratium, Aphonopelma hollyi, Aphonopelma mordax, Aphonopelma radinum, Aphonopelma rusticum, Aphonopelma texense). Our proposed species tree based on Anchored Enrichment data delimits five major lineages: a monotypic group confined to California, a western group, an eastern group, a group primarily distributed in high-elevation areas, and a group that comprises several miniaturized species. Multiple species are distributed throughout two biodiversity hotspots in the United States (i.e., California Floristic Province and Madrean Pine-Oak Woodlands). Keys are provided for identification of both males and females. By conducting the most comprehensive sampling of a single theraphosid genus to date, this research significantly broadens the scope of prior molecular and morphological investigations, finally bringing a modern understanding of species delimitation in this dynamic and charismatic group of spiders.     

Review of Gasteruption Latreille (Hymenoptera,Gasteruptiidae) from Iran and Turkey,with the description of 15 new species

The genus Gasteruption Latreille, 1796 (Hymenoptera: Evanioidea: Gasteruptiidae: Gasteruptiinae) from North Iran and Turkey is revised, keyed and fully illustrated for the first time. In total 36 species are treated of which 33 are recorded from Turkey and 23 from Iran. Fifteen species are new for science: Gasteruption aciculatum van Achterberg, sp. n., Gasteruption agrenum van Achterberg, sp. n., Gasteruption brevibasale van Achterberg & Saure, sp. n., Gasteruption coriacoxale van Achterberg, sp. n., Gasteruption flavimarginatum van Achterberg, sp. n., Gasteruption heminitidum van Achterberg, sp. n., Gasteruption henseni van Achterberg, sp. n., Gasteruption ischnolaimum van Achterberg, sp. n., Gasteruption nigrapiculatum van Achterberg, sp. n., Gasteruption paglianoi van Achterberg & Saure, sp. n., Gasteruption pseudolaticeps van Achterberg, sp. n., Gasteruption punctifrons van Achterberg, sp. n., Gasteruption schmideggeri van Achterberg & Saure, sp. n., Gasteruption scorteum van Achterberg, sp. n. and Gasteruption smitorum van Achterberg, sp. n. Twenty-one species are reported new for Turkey and 16 species new for Iran. Fifteen new synonyms are proposed: Foenus terrestris Tournier, 1877, Gasteruption trifossulatum Kieffer, 1904, and Gasteruption ignoratum Kieffer, 1912, of Gasteruption caucasicum (Guérin-Méneville, 1844); Gasteruption daisyi Alekseev, 1993, of Gasteruption dolichoderum Schletterer, 1889; Gasteruption assectator var. nitidulum Schletterer, 1885, of Gasteruption freyi (Tournier, 1877); Gasteruption schossmannae Madl, 1987, of Gasteruption hastator (Fabricius, 1804); Gasteryption fallaciosum Semenov, 1892, Gasteruption dubiosum Semenov, 1892 and Gasteruption obsoletum Semenov, 1892, of Gasteruption insidiosum Semenov, 1892; Gasteryption schewyrewi Semenov, 1892, of Gasteruption jaculator (Linnaeus, 1758); Gasteruption floreum Szépligeti, 1903, of Gasteruption lugubre Schletterer, 1889; Gasteruption trichotomma Kieffer, 1904, and Gasteruption palaestinum Pic, 1916, of Gasteruption merceti Kieffer, 1904; Gasteryption foveiceps Semenov, 1892, of Gasteruption nigrescens Schletterer, 1885, and Gasteruption libanense Pic, 1916, of Gasteruption syriacum Szépligeti, 1903. Gasteruption lugubre Schletterer, 1889, is recognised as a valid species. Lectotypes are designated for Ichneumon assectator Linnaeus, 1758; Ichneumon jaculator Linnaeus, 1758; Foenus terrestris Tournier, 1877; Foenus freyi Tournier, 1877; Foenus nigripes Tournier, 1877; Foenus goberti Tournier, 1877; Foenus granulithorax Tournier, 1877; Foenus minutus Tournier, 1877; Foenus borealis Thomson, 1883; Faenus diversipes Abeille de Perrin, 1879; Foenus rugulosus Abeille de Perrin, 1879; Faenus obliteratus Abeille de Perrin, 1879; Faenus undulatum Abeille de Perrin, 1879; Faenus variolosus Abeille de Perrin, 1879; Gasteruption distinguendum Schletterer, 1885; Gasteruption laeviceps Schletterer, 1885; Gasteruption thomsonii Schletterer, 1885; Gasteruption foveolatum Schletterer, 1889; Gasteruption sowae Schletterer, 1901; Gasteruption foveolum Szépligeti, 1903; Gasteruption floreum Szépligeti, 1903; Gasteruption caudatum Szépligeti, 1903; Gasteruption syriacum Szépligeti, 1903; Gasteruption merceti Kieffer, 1904 and Gasteruption ignoratum Kieffer, 1912. A neotype is designated for Gasteruption tournieri Schletterer, 1885.     

A taxonomic review on the species of Tetraserica Ahrens, 2004, of China (Coleoptera,Scarabaeidae, Sericini)

A review on the Chinese species of Tetraserica Ahrens, 2004, is presented. The lectotype of Tetraserica tonkinensis (Moser, 1908), comb. n. is designated. Twenty-nine new Tetraserica species are described from China and adjacent regions: Tetraserica anhuaensis sp. n., Tetraserica changjiangensis sp. n., Tetraserica changshouensis sp. n., Tetraserica damaidiensis sp. n., Tetraserica daqingshanica sp. n., Tetraserica fikaceki sp. n., Tetraserica graciliforceps sp. n., Tetraserica jinghongensis sp. n., Tetraserica leishanica sp. n., Tetraserica liangheensis sp. n., Tetraserica linaoshanica sp. n., Tetraserica longipenis sp. n., Tetraserica longzhouensis sp. n., Tetraserica maoershanensis sp. n., Tetraserica mengeana sp. n., Tetraserica menglongensis sp. n., Tetraserica pingjiangensis sp. n., Tetraserica ruiliana sp. n., Tetraserica ruiliensis sp. n., Tetraserica sculptilis sp. n., Tetraserica shangsiensis sp. n., Tetraserica shunbiensis sp. n., Tetraserica sigulianshanica sp. n., Tetraserica tianchiensis sp. n., Tetraserica wandingensis sp. n., Tetraserica wangtongensis sp. n., Tetraserica xichouensis sp. n., Tetraserica yaoanica sp. n., Tetraserica yaoquensis sp. n. A key to the Chinese Tetraserica species is given, species distribution as well as the habitus and male genitalia of all species are illustrated.     

Revision of the genus Menevia Schaus, 1928 (Lepidoptera,Mimallonoidea, Mimallonidae) with the description of 11 new species

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.     

Revision of the Lacinipolia vicina (Grote) complex (Noctuidae,Noctuinae, Eriopygini)

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.     

Integrative taxonomy of New World Euplectrus Westwood (Hymenoptera,Eulophidae), with focus on 55 new species from Area de Conservación Guanacaste,northwestern Costa Rica

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.     

Description of six new species of Lycocerus Gorham (Coleoptera,Cantharidae), with taxonomic note and new distribution data of some other species

Six new species of Lycocerus Gorham are described, Lycocerus gracilicornis sp. n. (China: Sichuan), Lycocerus longihirtus sp. n. (China: Yunnan), Lycocerus sichuanus sp. n. (China: Sichuan), Lycocerus hubeiensis sp. n. (China: Hubei), Lycocerus napolovi sp. n. (Vietnam: Sa Pa) and Lycocerus quadrilineatus sp. n. (Vietnam: Sa Pa), and provided with illustrations of habitus, antennae and aedeagi of male or and antennae, abdominal sternites VIII and genitalia of female. Lycocerus rubroniger Švihla, 2011 is synonymized with Lycocerus obscurus Pic, 1916. Lycocerus hickeri Pic, 1934 and Lycocerus obscurus are provided with illustrations of abdominal sternites VIII of female. Nine species are recorded from China for the first time, Lycocerus bicoloripennis (Pic, 1924), Lycocerus caliginostus Gorham, 1889, Lycocerus jendeki Švihla, 2005, Lycocerus malaisei (Wittmer, 1995), Lycocerus obscurus, Lycocerus olivaceus (Wittmer, 1995), Lycocerus purpureus Kazantsev, 2007, Lycocerus ruficornis (Wittmer, 1995) and Lycocerus semiextensus (Wittmer, 1995), and Lycocerus ruficornis is also recorded for Myanmar for the first time.     

Annotated type catalogue of the Megaspiridae,Orthalicidae, and Simpulopsidae (Mollusca,Gastropoda, Orthalicoidea) in the Natural History Museum,London

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).     

Melithaeidae of Japan (Octocorallia,Alcyonacea) re-examined with descriptions of 11 new species

Japanese melithaeid type material is re-examined and re-described. The sclerites of the different species are depicted using Scanning Electron Microscopy. All Japanese species of the family Melithaeidae treated here belong to the genus Melithaea and are endemic to Japanese waters. Old museum material and newly collected specimens from Japanese waters are identified after comparison with this type material. Acabaria modesta var. abyssicola is regarded a separate species, here named Melithaea abyssicola (Kükenthal, 1909). In addition, 11 new species are described: Melithaea boninensis sp. n., Melithaea doederleini sp. n., Melithaea isonoi sp. n., Melithaea keramaensis sp. n., Melithaea oyeni sp. n., Melithaea ryukyukensis sp. n., Melithaea sagamiensis sp. n., Melithaea satsumaensis sp. n., Melithaea suensoni sp. n., Melithaea tanseii sp. n., and Melithaea tokaraensis sp. n.. Pleurocorallium confusum Moroff, 1902, Pleurocoralloides formosum Moroff, 1902, Melitodes flabellifera Kükenthal, 1908, and Melitodes densa Kükenthal, 1908 are synonymized with Melithaea japonica (Verrill, 1865). We have designated a neotype for Melithaea mutsu Minobe, 1929. A key to the Japanese melithaeids is presented.     

Ninety-eight new species of Trigonopterus weevils from Sundaland and the Lesser Sunda Islands

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.     

Annotated type catalogue of the Chrysididae (Insecta,Hymenoptera) deposited in the collection of Radoszkowski in the Polish Academy of Sciences,Kraków

A critical and annotated catalogue of 183 types of Hymenoptera Chrysididae belonging to 124 taxa housed in the Radoszkowski collection is given. Radoszkowski type material from other institutes has also been checked. Six lectotypes are designated in Kraków (ISEA-PAN): Chrysis acceptabilis Radoszkowski, 1891; Chrysis persica Radoczkowsky, 1881; Chrysis daphnis Mocsáry, 1889; Chrysis lagodechii Radoszkowski, 1889; Chrysis remota Mocsáry, 1889 and Chrysis vagans Radoszkowski, 1877. The lectotype of Brugmoia pellucida Radoszkowski, 1877 is designated in Moscow (MMU). Four new combinations are proposed: Philoctetes araraticus (Radoszkowski, 1890), comb. n.; Pseudomalus hypocrita (du Buysson, 1893), comb. n.; Chrysis eldari (Radoszkowski, 1893), comb. n.; and Chrysura mlokosewitzi (Radoszkowski, 1889), comb. n.. Ten new synonyms are given: Chrysis auropunctata Mocsáry, 1889, syn. n. of Chrysis angolensis Radoszkovsky, 1881; Chrysis chrysochlora Mocsáry, 1889, syn. n. and Chrysis viridans Radoszkowski, 1891, syn. n. of Chrysis keriensis Radoszkowski, 1887; Chrysis angustifrons var. ignicollis Trautmann, 1926, syn. n. of Chrysis eldari (Radoszkowski, 1893); Chrysis maracandensis var. simulatrix Radoszkowski, 1891, syn. n. of Chrysis maracandensis Radoszkowski, 1877; Chrysis pulchra Radoszkovsky, 1880, syn. n. of Spinolia dallatorreana (Mocsáry, 1896); Chrysis rubricollis du Buysson, 1900, syn. n. of Chrysis eldari (Radoszkowski, 1893); Chrysis subcoerulea Radoszkowski, 1891, syn. n. of Chrysis chlorochrysa Mocsáry, 1889; Chrysis therates Mocsáry, 1889, syn. n. of Chrysis principalis Smith, 1874; and Notozus komarowi Radoszkowski, 1893, syn. n. of Elampus obesus (Mocsáry, 1890). One species is revaluated: Chrysis chalcochrysa Mocsáry, 1887. Chrysis kizilkumiana Rosa is the new name for Chrysis uljanini Radoszkowski & Mocsáry, 1889 nec Radoszkowski, 1877. Pictures of seventy-seven type specimens are given.     

The genera in the second catalogue (1833–1836) of?Dejean’s Coleoptera collection

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.     

A survey of linyphiid spiders from Xishuangbanna,Yunnan Province,China (Araneae,Linyphiidae)

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.     

Trophic relations of Opatrum sabulosum (Coleoptera,Tenebrionidae) with leaves of cultivated and uncultivated species of herbaceous plants under laboratory conditions

We carried out a quantitative assessment of the consumption of herbaceous plants by Opatrum sabulosum (Linnaeus, 1761) – a highly significant agricultural pest species. We researched the feeding preferences of this pest species with respect to 33 uncultivated and 22 cultivated plant species. This species of darkling beetle feeds on many uncultivated plant species, including those with hairy leaves and bitter milky sap, such as Scabiosa ucrainca (5.21 mg/specimen/24 hours), Euphorbia virgata (3.45), Solanum nigrum (3.32), Centauria scabiosa (2.47), Lamium album (2.41), Aristolochia clematitis (1.76), Chenopodium album (1.73), Arctium lappa (1.51), Asperula odorata (1.20). A high rate of leaf consumption is also characteristic for cultivated species, for example, Perilla nankinensis (5.05 mg/specimen/24 hours), Lycopersicon esculentum (3.75), Tropaeolum majus (3.29), Nicotiana tabacum (2.66), Rumex acetosa (1.96), Beta vulgaris (1.27). Opatrum sabulosum is capable of feeding on plants which are poisonous to cattle. This species of darkling beetle consumes 95.5% of the cultivated and 48.5% of the uncultivated herbaceous plants researched.     

Taxonomy and distribution of some katydids (Orthoptera Tettigoniidae) from tropical Africa

Results of the study of specimens collected in tropical Africa and preserved in different European collections and museums are reported and extensively illustrated. The following three new species are described: Horatosphaga aethiopica sp. n., Dapanera occulta sp. n. and Cestromoecha laeglae sp. n. In addition, new diagnostic characters or distributional data for Ruspolia differens (Serville, 1838), Thyridorhoptrum senegalense Krauss, 1877, Horatosphaga leggei (Kirby, 1909), Horatosphaga linearis (Rehn, 1910), Preussia lobatipes Karsch, 1890 and Dapanera eidmanni Ebner, 1943 are reported. Finally, Symmetropleura plana (Walker, 1869) is proposed to be transferred to the genus Symmetrokarschia Massa, 2015, Conocephalus carbonarius (Redtenbacher, 1891) to the genus Thyridorhoptrum Rehn & Hebard, 1915; the genus Gonatoxia Karsch, 1889 is proposed to be synonymized with Dapanera Karsch, 1889.     

Resolution of taxonomic problems in Australian Harpalini,Abacetini, Pterostichini,and Oodini (Coleoptera,Carabidae)

Taxonomic changes are made for several problematic Australian Carabidae in the tribes Harpalini, Abacetini, Pterostichini, and Oodini. Examination of types resulted in the synonymy of Veradia Castelnau, 1867 with Leconomerus Chaudoir, 1850; Nelidus Chaudoir, 1878, Feronista Moore, 1965, and Australomasoreus Baehr, 2007 with Cerabilia Castelnau, 1867; and newly combining Fouquetius variabilis Straneo, 1960 in the genus Pediomorphus Chaudoir, 1878; Australomasoreus monteithi Baehr, 2007 in the genus Cerabilia Castelnau, 1867; and Anatrichis lilliputana W.J. Macleay, 1888 in the genus Nanodiodes Bousquet, 1996. Cuneipectus Sloane, 1907 is placed in Pterostichini Bonelli, 1810, which is a senior synonym of Cuneipectini Sloane, 1907.