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.     

An annotated catalogue of the types of Chrysididae (Hymenoptera) at the Swedish Museum of Natural History,Stockholm, with brief historical notes

A critical and annotated catalogue of 72 types of Chrysididae (Hymenoptera) belonging to 53 species and subspecies housed in the Swedish Museum of Natural History is given. The lectotypes of Chrysis diversa Dahlbom, 1845, Chrysis soror Dahlbom, 1854, Chrysura sulcata Dahlbom, 1845 and Holopyga amoenula Dahlbom, 1845 are designated. The previous lectotype of Chrysis diversa Dahlbom, 1845 is set aside. Five new synonymies are proposed: Chrysis elegans var. smaragdula Trautmann, 1926 (currently Chrysis elegans ssp. interrogata Linsenmaier, 1959 repl. name for smaragdula Trautmann, nec Fabricius, 1775), syn. n. of Chrysis confluens (Dahlbom, 1845); Chrysis eximia Mocsáry, 1889, syn. n. of Chrysis poecila Mocsáry, 1889; Chrysis pyrrhina Dahlbom, 1845, syn. n. of Chrysis erythromelas Dahlbom, 1845; Chrysis separata Trautmann, 1926, syn. n. of Chrysis lateralis Dahlbom, 1845; Chrysis sicula Abeille de Perrin, 1877, syn. n. of Chrysis erythromelas Dahlbom, 1845. Chrysis serena Radoszkowski, 1891 is the first available name for Chrysis pyrrhina sensu auctorum. Chrysis erythromelas Dahlbom, 1845 is revaluated as valid species. The neotype of Chrysis inaequalis Dahlbom, 1845 is designated in the Linsenmaier collection (NMLS). Illustrations of 34 types are given.     

Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera,Tineoidea)

The New World genus Philonome Chambers, 1874 is revised. This genus comprises twelve species, seven of which are described as new: two species, Philonome nigrescens sp. n. and Philonome wielgusi sp. n., from the United States; four species, Philonome albivittata sp. n., Philonome curvilineata sp. n., Philonome kawakitai sp. n., and Philonome lambdagrapha sp. n., from French Guiana; and one species, Philonome penerivifera sp. n., from Brazil. Lectotypes are designated for Philonome clemensella Chambers, 1874 and Philonome rivifera Meyrick, 1915. Partially on evidence of their head morphology and particularly from molecular evidence, the genus Philonome, previously associated with Bucculatricidae or Lyonetiidae, is reassigned to Tineidae. A possible systematic position of Philonome within Tineidae is discussed. Eurynome Chambers, 1875, is synonymized with Argyresthia Hübner, 1825 (Argyresthiidae). Photographs of adults and illustrations of genitalia, when available, are provided for all described species of Philonome and two species previously misplaced in Philonome, Argyresthia luteella (Chambers, 1875) and Elachista albella (Chambers, 1877). In addition, DNA barcodes were used for the delimitation of most species.     

Notes on the genus Xenocerogria (Coleoptera,Tenebrionidae, Lagriini) from China

Three species of the genus Xenocerogria Merkl, 2007 have been recorded in China, Xenocerogria feai (Borchmann, 1911), Xenocerogria ignota (Borchmann, 1941) and Xenocerogria ruficollis (Borchmann, 1912). Xenocera xanthisma Chen, 2002 is proposed as a junior synonym of Xenocerogria ruficollis. Lectotype of Xenocerogria ignota is designated, and the species is transferred to the genus Lagria Fabricius, 1775. New Chinese province records of Xenocerogria ruficollis are provided.     

New genera,species and records of Phaneropterinae (Orthoptera,Phaneropteridae) from sub-Saharan Africa

The results of the study of many specimens preserved in different European museums are reported. The tribe Terpnistrini Brunner von Wattenwyl, 1878 is resurrected. The distribution of the following species is enhanced: Pardalota asymmetrica Karsch, 1896, Diogena denticulata Chopard, 1954, Diogena fausta (Burmeister, 1838), Plangiopsis adeps Karsch, 1896, Poreuomena sanghensis Massa, 2013 and Tylopsis continua (Walker, 1869). Further, for their peculiar characteristics, two African representatives of the American genus Symmetropleura Brunner von Wattenwyl, 1878 are included in two new genera: Symmetrokarschia africana (Brunner von Wattenwyl, 1878), comb. n. and Symmetroraggea dirempta (Karsch, 1889), comb. n. A new genus and species from the Democratic Republic of Congo, Angustithorax spiniger gen. n., sp. n., and a new genus and species from Tanzania, Arostratum oblitum gen. n., sp. n. are described. Finally Melidia claudiae sp. n. and Atlasacris brevipennis sp. n. are described and compared with related species.     

Revision of the Australian species of the weevil genus Trigonopterus Fauvel

The Australian species of the genus Trigonopterus Fauvel are revised. Eight previously recognized species are redescribed and 24 additional new species are described: Trigonopterus allaetus Riedel, sp. n., Trigonopterus athertonensis Riedel, sp. n., Trigonopterus australinasutus Riedel, sp. n., Trigonopterus australis Riedel, sp. n., Trigonopterus bisignatus Riedel, sp. n., Trigonopterus bisinuatus Riedel, sp. n., Trigonopterus boolbunensis Riedel, sp. n., Trigonopterus cooktownensis Riedel, sp. n., Trigonopterus daintreensis Riedel, sp. n., Trigonopterus deplanatus Riedel, sp. n., Trigonopterus finniganensis Riedel, sp. n., Trigonopterus fraterculus Riedel, sp. n., Trigonopterus garradungensis Riedel, sp. n., Trigonopterus hasenpuschi Riedel, sp. n., Trigonopterus hartleyensis Riedel, sp. n., Trigonopterus kurandensis Riedel, sp. n., Trigonopterus lewisensis Riedel, sp. n., Trigonopterus montanus Riedel, sp. n., Trigonopterus monteithi Riedel, sp. n., Trigonopterus mossmanensis Riedel, sp. n., Trigonopterus oberprieleri Riedel, sp. n., Trigonopterus robertsi Riedel, sp. n., Trigonopterus terraereginae Riedel, sp. n., Trigonopterus yorkensis Riedel, sp. n.. All new species are authored by the taxonomist-in-charge, Alexander Riedel. Lectotypes are designated for the following names: Idotasia aequalis Pascoe, Idotasia albidosparsa Lea, Idotasia evanida Pascoe, Idotasia laeta Lea, Idotasia rostralis Lea, Idotasia sculptirostris Lea, Idotasia squamosa Lea. A new combination of the name Idotasia striatipennis Lea is proposed: Trigonopterus striatipennis (Lea), comb. n.. A key to the species is provided. Australian Trigonopterus occur in coastal Queensland, narrowly crossing into New South Wales. The southern parts of the range are inhabited by species found on foliage. A rich fauna of 19 edaphic species inhabiting the leaf litter of tropical forests is reported for the first time from the Australian Wet Tropics.     

A review of the omicrine genera Omicrogiton,Mircogioton and Peratogonus of China (Coleoptera,Hydrophilidae, Sphaeridiinae)

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.     

Systematics of the parasitic wasp genus Oxyscelio Kieffer (Hymenoptera,Platygastridae s.l.), part III: African fauna

African species of Oxyscelio (Hymenoptera: Platygastridae s.l.) are revised. A total of 14 species are recognized, 13 of which are described as new: Oxyscelio absentiae Burks, sp. n., Oxyscelio galeri Burks, sp. n., Oxyscelio gyri Burks, sp. n., Oxyscelio idoli Burks, sp. n., Oxyscelio intensionis Burks, sp. n., Oxyscelio io Burks, sp. n., Oxyscelio kylix Burks, sp. n., Oxyscelio lunae Burks, sp. n., Oxyscelio nemesis Burks, sp. n., Oxyscelio pulveris Burks, sp. n., Oxyscelio quassus Burks, sp. n., Oxyscelio teli Burks, sp. n. and Oxyscelio xenii Burks, sp. n. The genus Freniger Szabó, syn. n. is recognized as part of an endemic African species group of Oxyscelio with incomplete hind wing venation, and Oxyscelio bicolor (Szabó), comb. n. is therefore recognized as the only previously described species of Oxyscelio from Africa. The Oxyscelio crateris and Oxyscelio cuculli species groups, previously known from southeast Asia, are represented in Africa by seven and one species respectively.     

Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia

The diversity of Diplopoda in caves of southern China is remarkably high, often 5–6 species per cave, consisting mostly of local endemics and presumed troglobionts. These are evidently biased to just a few lineages, mainly members of the orders Chordeumatida and Callipodida, the families Cambalopsidae (Spirostreptida) and Haplodesmidae (Polydesmida) or the genera Pacidesmus, Epanerchodus and Glenniea (all Polydesmida, Polydesmidae), Trichopeltis (Polydesmida, Cryptodesmidae), Dexmoxytes (Polydesmida, Paradoxosomatidae) and Hyleoglomeris (Glomerida, Glomeridae). All these taxa, especially the Paradoxosomatidae and Cambalopsidae (usually amounting to about 60% and 10% of the total species diversity in the Oriental fauna, respectively), are moderately to highly speciose across Southeast Asia, being largely epigean. However, the epigean Diplopoda of southern China are yet badly understudied, since much of the collecting and taxonomic exploration efforts still focus on cavernicoles. The Oriental Region is the only biogeographic realm globally that harbours all 16 orders of Diplopoda, of which 14 have already been encountered in China and/or the immediately adjacent parts of Indochina. Thus, China may actually prove to support no less than 1,000 millipede species of various origins, mainly Oriental and Palaearctic.     

Revision of the Ceratocapsine Renodaeus group: Marinonicoris,Pilophoropsis, Renodaeus,and Zanchisme,with descriptions of four new genera (Heteroptera,Miridae, Orthotylinae)

The Renodaeus group, a monophyletic assemblage of genera within the New World orthotyline tribe Ceratocapsini, comprising eight genera, including four new ones, is defined; and 48 species are treated, including 26 described as new and 12 transferred from Ceratocapsus Reuter as new combinations. Ceratocapsidea gen. n. is described to accommodate the new species Ceratocapsidea bahamaensis sp. n., from the Bahamas; Ceratocapsidea baranowskii sp. n., from Jamaica; Ceratocapsidea dominicanensis sp. n., from the Dominican Republic; Ceratocapsidea rileyi sp. n., from Texas; Ceratocapsidea taeniola sp. n., from Jamaica; Ceratocapsidea texensis sp. n., from Texas; Ceratocapsidea transversa sp. n., from Mexico (Neuvo León); and Ceratocapsidea variabilis sp. n., from Jamaica; and Ceratocapsus balli Knight, comb. n., Ceratocapsus complicatus Knight, comb. n., Ceratocapsidea consimilis Reuter, comb. n., Ceratocapsus fusiformis Van Duzee, comb. n. (as the type species of the genus), Ceratocapsus nigropiceus Reuter, comb. n., and Ceratocapsus rufistigmus Blatchley, comb. n. [and a neotype designated], Ceratocapsus clavicornis Knight, syn. n. and Ceratocapsus divaricatus Knight, syn. n. are treated as junior synonyms of Ceratocapsus fusiformis Van Duzee. The genus Marininocoris Carvalho and the only included species Marinonicoris myrmecoides Carvalho are redescribed. The genus Pilophoropsis Poppius is redescribed and revised, Renodaeus texanus Knight, comb. n. is transferred into it and the three new species Pilophoropsis bejeanae sp. n., from Sonora, Mexico; Pilophoropsis cunealis sp. n., from Oaxaca, Mexico; Pilophoropsis quercicola sp. n., from Arizona, USA, are described. Pilophoropsidea gen. n. is described to accommodate the 12 new species Pilophoropsidea brailovskyi sp. n., from Federal District, Mexico; Pilophoropsidea cuneata sp. n., from Chiapas, Mexico; Pilophoropsidea dimidiata sp. n., from Durango, Mexico; Pilophoropsidea fuscata sp. n., from Durango, Mexico and Arizona and New Mexico, USA; Pilophoropsidea keltoni sp. n., from Durango, Mexico; Pilophoropsidea maxima sp. n., from Durango, Mexico; Pilophoropsidea pueblaensis sp. n., from Puebla, Mexico; Pilophoropsidea schaffneri sp. n., from Neuvo León and San Luis Potosi, Mexico; Pilophoropsidea serrata sp. n., from Michoacan, Mexico; Pilophoropsidea touchetae sp. n., from Mexico (Puebla); Pilophoropsidea truncata sp. n., from Mexico (Guerrero); Pilophoropsidea tuberculata sp. n., from Mexico (Guerrero); and Ceratocapsus barberi Knight, comb. n., Ceratocapsus camelus Knight, comb. n. (as the type species of the genus), and Ceratocapsus fascipennis Knight, comb. n. Pilophoropsita gen. n. is described to accommodate Pilophoropsidea schaffneri sp. n. from Costa Rica and Mexico (Jalisco, Nayarit, Oaxaca). The genus Renodaeus Distant is redescribed and the new species Renodaeus mimeticus sp. n. from Ecuador is described. The genus Zanchisme Kirkaldy is reviewed and the four known species are redescribed. Zanchismeopsidea gen. n. is described to accommodate Zanchismeopsidea diegoi sp. n. from Argentina (Santiago del Estero). Provided are habitus illustrations for certain adults (Pilophoropsidea camelus, Pilophoropsis brachyptera Poppius, Renodaeus mimeticus, and Zanchisme mexicanus Carvalho & Schaffner), male and female (when available) color digital images and figures of male genitalia of all species, electron photomicrographs of diagnostic characters for selected species, and keys to the genera and their included species. The taxa treated in this paper are arranged alphabetically by genus and species.     

The genus Gymnetron from China with description of pre-imaginal stages of G. miyoshii,G. auliense and G. vittipenne (Coleoptera,Curculionidae)

There are four species of Gymnetron in China recorded to date including Gymnetron miyoshii Miyoshi, 1922, Gymnetron villosipenne Roelofs, 1875, Gymnetron auliense Reitter, 1907 and Gymnetron vittipenne Marseul, 1876, of which the last two are new country records. The pre-imaginal stages including eggs, mature larvae and pupae of Gymnetron miyoshii, Gymnetron auliense and Gymnetron vittipenne are described and illustrated. In addition, their diagnostic characters (larvae and pupae) are discussed and differentiated, and notes on some of their biological parameters are provided. Potential ecological impacts between Gymnetron weevils and their host Veronica spp. also are provided.     

Taxonomy of Fissocantharis Pic (Coleoptera,Cantharidae) from Guangxi,China, with descriptions of six new species

A total of 17 species of Fissocantharis Pic is recorded from Guangxi, China. Six species are described new to science, Fissocantharis sinensomima sp. n., Fissocantharis sexcostata sp. n., Fissocantharis basilaris sp. n., Fissocantharis eschara sp. n., Fissocantharis latipalpa sp. n. and Fissocantharis biprojicientis sp. n., and two previously known species are redescribed, Fissocantharis gracilipes (Pic, 1927) and Fissocantharis sinensis (Wittmer, 1988). These species are presented with habitus of males, abdominal sternites VIII of females and genitalia of both sexes. Fissocantharis flavofacialis (Pic, 1926) is synonymized with Fissocantharis angusta (Fairmaire, 1900); both were originally described in the genus Podabrus Westwood. Additionally, a key and a checklist of all the species of Fissocantharis from Guangxi are provided.     

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).     

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).     

The subtribes and genera of the tribe Listroderini (Coleoptera,Curculionidae, Cyclominae): Phylogenetic analysis with systematic and biogeographical accounts

The phylogenetic relationships of the genera of Listroderini LeConte, 1876 are analyzed based on 58 morphological characters. The genera are grouped in four clades, which are given subtribal status: Macrostyphlina new subtribe (Adioristidius, Amathynetoides, Andesianellus, Macrostyphlus, Nacodius and Puranius), Palaechthina Brinck, 1948 (Anorthorhinus, Gunodes, Haversiella, Inaccodes, Listronotus, Neopachytychius, Palaechthus, Palaechtodes, Steriphus and Tristanodes), Falklandiina new subtribe (Falklandiellus, Falklandiopsis, Falklandius, Gromilus, Lanteriella, Liparogetus, Nestrius and Telurus), and Listroderina (Acroriellus, Acrorius, Acrostomus, Antarctobius, Germainiellus, Hyperoides, Lamiarhinus, Listroderes, Methypora, Philippius, Rupanius and Trachodema). The subtribes are characterized and keys to identify them and their genera are provided. Listroderini have four main biogeographical patterns: Andean (Macrostyphlina), Andean-New Zealand (Falklandiina), Andean-Neotropical-Australian (Listroderina) and Andean-Neotropical-Australian-New Zealand-Nearctic-Tristan da Cunha-Gough islands (Palaechthina). Geographical paralogy, particularly evident in the Subantarctic subregion of the Andean region, suggests that Listroderini are an ancient Gondwanic group, in which several extinction events might have obscured relationships among the areas.     

Review of the millipede genus Eutrichodesmus Silvestri, 1910, in China,with descriptions of new cavernicolous species (Diplopoda,Polydesmida, Haplodesmidae)

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.     

Systematics of the family Plectopylidae in Vietnam with additional information on Chinese taxa (Gastropoda,Pulmonata, Stylommatophora)

Vietnamese species from the family Plectopylidae are revised based on the type specimens of all known taxa, more than 600 historical non-type museum lots, and almost 200 newly-collected samples. Altogether more than 7000 specimens were investigated. The revision has revealed that species diversity of the Vietnamese Plectopylidae was previously overestimated. Overall, thirteen species names (anterides Gude, 1909, bavayi Gude, 1901, congesta Gude, 1898, fallax Gude, 1909, gouldingi Gude, 1909, hirsuta Möllendorff, 1901, jovia Mabille, 1887, moellendorffi Gude, 1901, persimilis Gude, 1901, pilsbryana Gude, 1901, soror Gude, 1908, tenuis Gude, 1901, verecunda Gude, 1909) were synonymised with other species. In addition to these, Gudeodiscus hemmeni sp. n. and Gudeodiscus messageri raheemi ssp. n. are described from north-western Vietnam. Sixteen species and two subspecies are recognized from Vietnam. The reproductive anatomy of eight taxa is described. Based on anatomical information, Halongella gen. n. is erected to include Plectopylis schlumbergeri and Plectopylis fruhstorferi. Additionally, the genus Gudeodiscus is subdivided into two subgenera (Gudeodiscus and Veludiscus subgen. n.) on the basis of the morphology of the reproductive anatomy and the radula. The Chinese Gudeodiscus phlyarius werneri Páll-Gergely, 2013 is moved to synonymy of Gudeodiscus phlyarius. A spermatophore was found in the organ situated next to the gametolytic sac in one specimen. This suggests that this organ in the Plectopylidae is a diverticulum. Statistically significant evidence is presented for the presence of calcareous hook-like granules inside the penis being associated with the absence of embryos in the uterus in four genera. This suggests that these probably play a role in mating periods before disappearing when embryos develop. Sicradiscus mansuyi is reported from China for the first time.