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Although cone snails are among the most studied group of gastropods, new species are still regularly described. Here, we focus on Afonsoconus Tucker & Tenorio, 2013, a lineage that includes only two species from the Indo-Pacific Ocean. The analysis of molecular (partial mitochondrial cox1 gene sequences) and morphological (shell and radular tooth) characters revealed that the samples collected by dredging in deep water during a recent expedition carried out in the Mozambique Channel are different from the samples collected in the Pacific Ocean. We thus introduce here a new species, Afonsoconus crosnieri sp. nov., from the SW Indian Ocean including records from the Mozambique Channel, the Comoros and Glorieuses Islands, Madagascar, South Africa and Reunion Island.
During a survey of the fishes in the region of the Wonga-Wongué Presidential Reserve, 14 new populations of the subgenus Chromaphyosemion Myers, 1924 were found. These observations extend the previously known distribution range of the subgenus 120 kilometres southward. None of these populations could be related to any described species. Based on the colouration of the males and females, together with a genetic marker (mitochondrial DNA cytochrome b sequences), the populations studied are grouped into six new species which are described in this article, all close to Aphyosemion alpha Huber, 1998 with which they share the presence of a black alpha-shaped mark on the pre- and post-opercular region. The group composed of A. alpha and the six new species is referred to here as the A. alpha species group. All the new species, A. aurantiacum Chirio, Legros & Agnèse sp. nov., A. barakoniense Chirio, Legros & Agnèse sp. nov., A. flammulatum Chirio, Legros & Agnèse sp. nov., A. flavocyaneum Chirio, Legros & Agnèse sp. nov., A. pusillum Chirio, Legros & Agnèse sp. nov. and A. rubrogaster Chirio, Legros & Agnèse sp. nov., are further unambiguously diagnosed by unique combinations of colour patterns, making it possible to generate an identification key for the A. alpha species group. It is likely that the coastal dunes of Wonga-Wongué that form a sandy relief, could have led to the fragmentation and then isolation of the hydrographical networks that flow into the Atlantic Ocean, making possible a significant number of allopatric speciations.
Three new species of Willowsia collected from Guizhou Province, China are described here: W. sexachaeta sp. nov., W. christianseni sp. nov., and W. tanae sp. nov. They have spinulate scales on the body. Colour pattern and dorsal chaetotaxy are the main diagnostic characters for these species. A table summarizing the main differences between all Chinese Willowsia species is given.
Twenty species of the genus Chilocorus Leach, 1815 currently known from China are recorded, including two new species described here: C. nigricaeruleus Li & Wang sp. nov. and C. strenotubus Li & Wang sp. nov. Diagnoses and detailed descriptions of the new species are given. Each species is illustrated in detail, including genitalia. Distribution maps, a key to the Chinese species and a world checklist of Chilocorus are given.
Comparison of morphological and genetic data from New Zealand forest cave wētā suggests we should recognise the genus Miotopus proposed by Hutton (1898). A new species within this genus is described (Miotopus richardsi sp. nov.). Both Miotopus diversus (Hutton, 1898) and Miotopus richardsi sp. nov. are common in native forests and widespread in New Zealand. Here we provide their known distributions and key traits.
Although extensively studied by different authors over the past 150 years, the taxonomy of Canthon Hoffmannsegg, 1817 and allied genera (which are here informally referred to as 'Canthon sensu lato') still remains problematic. With the aim of resolving some of the questions surrounding these taxa, the present work reviews the taxonomy of one of them, the genus Sylvicanthon Halffter & Martínez, 1977. As defined here, Sylvicanthon is distributed mainly throughout the vast areas of tropical rainforests in the Neotropical region and includes 15 species divided into two groups: the enkerlini group, with a single species, S. enkerlini (Martínez et al., 1964) comb. nov., and the candezei group, with five subgroups: the candezei subgroup, with S. candezei (Harold, 1869), S. genieri sp. nov. and S. foveiventris (Schmidt, 1920); the aequinoctialis subgroup, with S. aequinoctialis (Harold, 1868) comb. nov. and S. proseni (Martínez, 1949) stat. et comb. nov.; the bridarollii subgroup, with S. bridarollii (Martínez, 1949), S. seag sp. nov., S. edmondsi sp. nov. and S. attenboroughi sp. nov.; the furvus subgroup, with S. furvus (Schmidt, 1920), S. monnei sp. nov., S. mayri sp. nov. and S. obscurus (Schmidt, 1920); and the securus subgroup, with a single species, S. securus (Schmidt, 1920) comb. nov. Three species originally included in Sylvicanthon are here (re)transferred to Canthon: Canthon xanthopus Blanchard, 1846 and C. machadoi (Martínez & Pereira, 1967) comb. nov., as well as C. cobosi (Pereira & Martínez, 1960) stat. et comb. nov., which had been previously in synonymy under C. xanthopus. Descriptions, redescriptions, illustrations and comparative tables on the external morphology (including the genital capsule) of the genus and its species are presented, as well as a detailed discussion on their biogeography, comparative morphology, hypotheses on their phylogenetic relationships, data on natural history and a detailed historical revision of the classification of 'Canthon sensu lato'. Finally, we also discuss the socalled 'species problem' (i.e., the definition of the scientific term 'species') and its consequences to dung beetle taxonomy and favour the solution offered by the Biological Species Concept.
The family-group names of animals (superfamily, family, subfamily, supertribe, tribe and subtribe) are regulated by the International Code of Zoological Nomenclature. Particularly, the family names are very important, because they are among the most widely used of all technical animal names. A uniform name and spelling are essential for the location of information. To facilitate this, a list of familygroup names for fossil fishes has been compiled. I use the concept ‘Fishes’ in the usual sense, i.e., starting with the Agnatha up to the †Osteolepidiformes. All the family-group names proposed for fossil fishes found to date are listed, together with their author(s) and year of publication. The main goal of the list is to contribute to the usage of the correct family-group names for fossil fishes with a uniform spelling and to list the author(s) and date of those names. No valid family-group name description could be located for the following family-group names currently in usage: †Brindabellaspidae, †Diabolepididae, †Dorsetichthyidae, †Erichalcidae, †Holodipteridae, †Kentuckiidae, †Lepidaspididae, †Loganelliidae and †Pituriaspididae.
A revision of the genus Cicynethus Simon, 1910 (Araneae, Zodariidae), a tale of colour patterns
(2018)
The genus Cicynethus Simon, 1910 is revised. Apart from the type species C. peringueyi Simon, 1893, only known from a juvenile, it contains five species, all of which are here described or redescribed based on adults: C. acer sp. nov. (♂♀), C. decoratus (Lawrence, 1952) comb. nov (♂), C. floriumfontis Jocqué, 1991 (♂♀), C. mossambicus sp. nov. (♂♀) and C. subtropicalis (Lawrence, 1952) comb. nov. (♂♀). The species are characterized by the genitalia, but also by the colour pattern. The distribution of the genus is extended to northern Mozambique. Cicynethus hongfuchui is transferred to Storenomorpha hongfuchui (Barrion, Barrion-Dupo & Heong, 2013) comb. nov. Cicynethus acanthopus Simon, 1910 is considered a species incertae sedis. A key to the species is provided.
Cochlostoma revised: the subgenus Lovcenia Zallot et al., 2015
(Caenogastropoda, Cochlostomatidae)
(2018)
Five species of the subgenus Lovcenia of Cochlostoma (Cochlostomatidae) are recognized, three of which are described as new to science: C. (L.) tropojanum sp. nov., C. (L.) jakschae sp. nov. and C. (L.) lanatum sp. nov. A lectotype is designated for C. (L.) erika (A.J. Wagner, 1906). The shell and the genital tracts are described for all species and the distributional data are summarized.
The ‘gigas’ group of dragon millipedes, formerly placed in the genus Desmoxytes Chamberlin, 1923, is revised and assigned to the new genus Gigaxytes gen. nov. Desmoxytes gigas Golovatch & Enghoff, 1994 is the type species of the new genus and is redescribed as G. gigas (Golovatch & Enghoff, 1994) gen. et comb nov. Three new species are described: G. fusca gen et sp. nov. from Thailand and Myanmar; G. parvoterga gen et sp. nov. and G. suratensis gen et sp. nov. from Thailand. All Gigaxytes species are endemic to small distribution areas in limestone habitats in South Thailand and South Myanmar. Illustrations of external morphological characters and an identification key to all known species are provided as well as a distribution map.
The ‘acantherpestes’ group of dragon millipedes, formerly placed in the genus Desmoxytes Chamberlin, 1923, is revised and assigned to the new genus Nagaxytes Srisonchai, Enghoff & Panha gen. nov. Desmoxytes acantherpestes Golovatch & Enghoff, 1994 is the type species of the new genus and is redescribed as N. acantherpestes (Golovatch & Enghoff, 1994) gen. et comb. nov. Three new species are described from Thailand: N. erecta Srisonchai, Enghoff & Panha gen. et sp. nov. and N. gracilis Srisonchai, Enghoff & Panha gen. et sp. nov. from Kanchanaburi Province, and N. spatula Srisonchai, Enghoff & Panha gen. et sp. nov. from Tak Province. All new species are endemic to western Thailand and all are restricted to limestone habitats. Complete illustrations of external morphological characters, an identification key, and a distribution map are provided.
A new species of the genus Birdantis Stål, 1863 (Hemiptera: Fulgoridae), B. bhaskarai sp. nov. from Larat Island (Tanimbar), is described. Birdantis collaris (Walker, 1870) stat. rev. and B. trilineata (Schmidt, 1926) stat. rev. are reinstated as valid species, respectively from status of subspecies and as junior synonym of B. delibuta Stål, 1863. These four species, as well as the other one previously described from the Maluku Islands, B. decens Stål, 1863, are illustrated from their type specimens. An identification key, a distribution map, illustrations of habitus and details of male genitalia are provided. The synonymy between Myrilla Distant, 1888 and Birdantis is formally reinstated and all species formerly placed in the subgenus Birdantis (Myrilla) are transferred to Birdantis sensu stricto. Birdantis is transferred to the subfamily Aphaeninae Blanchard, 1847 and now contains eighteen species distributed in Maluku (five species), New Guinea and neighbouring islands (ten species) and Australia
(three species).
The genus Disparalona Fryer, 1968 comprises a well-defined species complex, the hamatagroup, which might have sibling species in South America. This hamata-group needs urgent revision. Besides that, a complete morphological evaluation of the endemic species D. leptorhyncha (Daday, 1905) is lacking. Thus, the aim of the present study is to revise populations of species of the hamatagroup in South America and to redescribe D. leptorhyncha. Our findings pointed to an occurrence of species which are part of the Disparalona (Mixopleuroxus) linage. Currently, the Neotropics have the highest diversity to the genus, with three species of the hamata-complex – D. (M.) hamata (Birge, 1879), D. (M.) lucianae sp. nov., D. (M.) tenuispina sp. nov. – in addition to D. (M.) leptorhyncha. These species can be differentiated from each other by the morphology of their rostrum, labrum, and postabdomen.
Nanium Townes, 1967 is a small New World parasitoid wasp genus in the subfamily Ctenopelmatinae Förster, 1869 (Hymenoptera: Ichneumonidae). Previously, it comprised five species: one from North America and four from Costa Rica. The current study reviews the Neotropical species of the genus, and includes descriptions of two new species, N. medianum Reshchikov & Sääksjärvi sp. nov. from Ecuador and N. atitlanensis Reshchikov & Sääksjärvi sp. nov. from Guatemala. A key to the species is provided.
The new genus Neodiplopeltula gen. nov. is proposed to accommodate those species from the genus Diplopeltula Gerlach, 1950 that possess the following morphological characters: amphids in the shape of an elongated loop, a well-developed subcylindrical stoma and outstretched ovaries. The genus Diplopeltula is considered genus inquirendum et incertae sedis. Four species placed in Neodiplopeltula gen. nov. are redescribed. The following taxonomic changes are proposed: Neodiplopeltula asymmetrica (Allgén, 1935) gen. et comb. nov.; Neodiplopeltula barentsi (Steiner, 1916) gen. et comb. nov.; Neodiplopeltula bathmanni (Jensen, 1991) gen. et comb. nov.; Neodiplopeltula cuspidiboja (Leduc, 2017) gen. et comb. nov.; Neodiplopeltula indica (Gerlach, 1962) gen. et comb. nov.; Neodiplopeltula intermedia (Gerlach, 1954) gen. et comb. nov.; Neodiplopeltula obesa (Nguyen Vu Thahn, Nguyen Thahn Hien & Gagarin, 2012) gen. et comb. nov.; Neodiplopeltula onusta (Wieser, 1956) gen. et comb. nov.; Neodiplopeltula ovalis (Ditlevsen, 1928) gen. et comb. nov. and Neodiplopeltula tchesunovi (Fadeeva & Mordukhovich, 2013) gen. et comb. nov. New synonyms include: Diplopeltis asymmetricus Allgén, 1935 and Diplopeltis ovalis Ditlevsen, 1928 are synonimised with Neodiplopeltula barentsi (Steiner, 1916) gen. et comb. nov.; Diplopeltula tchesunovi Fadeeva & Mordukhovich, 2013 is synonimised with Neodiplopeltula onusta (Wieser, 1956) gen. et comb. nov.; the male of Diplopeltula cuspidiboja Leduc, 2017 is synonimised with Neodiplopeltula barentsi gen. et comb. nov. and the female with N. bathmanni gen. et comb. nov. A key to the species of Neodiplopeltula gen. nov. is provided.
Umbyquyra gen. nov., a new Theraphosinae genus with stridulatory bristles on the palpal trocanther of pedipalp trochanter and first leg, is proposed. The genus differs from the other genera with stridulatory bristles on the same segments, Acanthoscurria Ausserer, 1871, Cyrtopholis Simon, 1892, Longilyra Gabriel, 2014 and Nesipelma Schmidt & Kovarik, 1996, by having a palpal bulb with a very short and acuminate embolus and four short keels; separated tibial apophysis; and female spermathecae resembling those of Cyrtopholis, with two seminal receptacles with elongated ducts emerging from a common area. Cyrtopholis palmarum Schiapelli & Gerschman, 1945 and C. schmidti Rudloff, 1996 from Brazil and Acanthoscurria acuminata Schmidt & Tesmoingt in Schmidt, 2005 from Bolivia are transferred to the new genus. The female of Umbyquyra palmarum (Schiapelli & Gerschman, 1945) gen. et comb. nov. and the male of U. schmidti (Rudloff, 1996) gen. et comb. nov. are described for the first time. Cyrtopholis zorodes Mello-Leitão, 1923 is considered a junior synonym of Acanthoscurria gomesiana Mello-Leitão, 1923 and Cyrtopholis meridionalis (Keyserling, 1891) is considered a nomen dubium. Eight new species from Brazil are described: Umbyquyra paranaiba gen. et sp. nov., U. cuiaba gen. et sp. nov., U. araguaia gen. et sp. nov., U. sapezal gen. et sp. nov., U. belterra gen. et sp. nov., U. caxiuana gen. et sp. nov., U. tucurui gen. et sp. nov. and U. tapajos gen. et sp. nov. Data and maps on the geographic distribution are provided.
The bathyal kinorhynch fauna along the Northwest American continental rise is explored, with emphasis on species of Echinoderidae Zelinka, 1894. Seven species of Echinoderes Claparède, 1863 are described as new to science: E. anniae sp. nov., E. dubiosus sp. nov., E. hamiltonorum sp. nov., E. hviidarum sp. nov., E. juliae sp. nov., E. lupherorum sp. nov. and E. yamasakii sp. nov. Three known species, Echinoderes hakaiensis Herranz, Yangel & Leander, 2017, E. cf. unispinosus Yamasaki, Neuhaus & George, 2018 and Fissuroderes higginsi Neuhaus & Blasche, 2006, are reported. The numerous new species indicate that the deep-sea still holds a great, undiscovered diversity of kinorhynchs, and that Echinoderes, as is also the case in more shallow, coastal waters, represents an important component of the deep-sea kinorhynch fauna. The presence of E. hakaiensis in the deepsea sediments demonstrates that the species may occur at a great depth range, and suggests that depth may play a less important role for the distribution of some kinorhynch species. The finding of the Northeast Atlantic species E. cf. unispinosus and the Southwest Pacific species Fissuroderes higginsi could indicate that kinorhynch species in the deep-sea may cover considerably larger distributional ranges than is assumed for coastal species of Echinoderidae.
The family Plectopylidae is divided into two subfamilies: Sinicolinae subfam. nov. (included extant genera: Gudeodiscus Páll-Gergely, 2013, Endothyrella Zilch, 1959, Halongella Páll-Gergely, 2015, Sicradiscus Páll-Gergely, 2013, Sinicola Gude, 1899) and Plectopylinae Möllendorff, 1898 (included genera: Chersaecia Gude, 1899, Hunyadiscus Páll-Gergely, 2016, Naggsia Páll-Gergely & Muratov, 2016, Plectopylis Benson, 1860). The Eocene fossil Plectopyloides Yen, 1969 is classified into the Sinicolinae. The Plectopylinae are revised mainly based on historical type and non-type material, and the material of the Florida Museum of Natural History, collected in Thailand in the 1980s. The following species-group taxa are described as new: Chersaecia auffenbergi sp. nov., Chersaecia densegyrata sp. nov., Chersaecia mogokensis sp. nov., Chersaecia reversalis sp. nov., Chersaecia scabra sp. nov., Chersaecia shiroiensis subnagaensis subsp. nov., Hunyadiscus tigrina sp. nov., Naggsia oligogyra sp. nov., Plectopylis crassilabris sp. nov., Plectopylis malayana sp. nov. and Plectopylis thompsoni sp. nov. The genus Endoplon Gude, 1899 is treated as a synonym of Chersaecia. Consequently, the two species classified in Endoplon are members of Chersaecia: Chersaecia brachyplecta (Benson, 1863) comb. nov. and Chersaecia smithiana (Gude, 1897) comb. nov. The genus Plectopylis is redefined, and includes only species with fused anterior and posterior lamellae. Thus, the following species are moved from Plectopylis to Chersaecia: Chersaecia feddeni (Blanford, 1865) comb. nov., Chersaecia goniobathmos (Ehrmann, 1922) comb. nov., Chersaecia leucochila (Gude, 1897) comb. nov., Chersaecia magna (Gude, 1897) comb. nov. and Chersaecia woodthorpei (Gude, 1899) comb. nov. Altogether thirteen species and varieties are moved to the synonymy of valid species: Helix (Plectopylis) brachydiscus Godwin-Austen, 1879 syn. nov., Helix (Plectopylis) ponsonbyi Godwin-Austen, 1888 syn. nov., Plectopylis (Chersaecia) kengtungensis Gude, 1914 syn. nov., Plectopylis (Chersaecia) degerbolae Solem, 1966 syn. nov., Plectopylis lissochlamys Gude, 1897 syn. nov., Helix repercussa Gould, 1856 syn. nov., Plectopylis achatina var. obesa Gude, 1898 syn. nov., Plectopylis achatina var. infrafasciata Gude, 1898 syn. nov. Plectopylis achatina var. venusta Gude, 1898 syn. nov., Plectopylis achatina var. castanea Gude, 1898 syn. nov., Plectopylis achatina var. breviplica Gude, 1898 syn. nov., Plectopylis achatina var. repercussoides Gude, 1899 syn. nov., Plectopylis linterae var. fusca Gude, 1898 syn. nov. Plectopylis (Chersaecia) simplex Solem, 1966 is a subspecies of Chersaecia perarcta (Blanford, 1865), whereas Plectopylis muspratti Gude, 1897 is a subspecies of Chersaecia nagaensis (Godwin-Austen, 1875).
Ants of the Tetramorium solidum group occur in Africa, with the vast majority of species endemic to the arid regions of southern Africa. The first revision of the genus was published more than 30 years ago and ant surveys have since considerably expanded the number of specimens available for study. The revision of this group reveals five new species, expanding the total number to 19. Almost all the species in this group occur in the southern parts of the Afrotropical region, with the exception of T. setuliferum Emery, 1895 and T. rothschildi (Forel, 1907). These two species have broad distributions within African grasslands and savannas, with T. setuliferum occurring in southern Africa and T. rothschildi in East Africa and the Sahel. Five new species are described in this revision: T. aisha sp. nov., T. brigitteae sp. nov., T. duncani sp. nov., T. lerouxi sp. nov. and T. margueriteae sp. nov. An illustrated key is presented and descriptions of new species are provided, supported by montage images and distribution maps.
Recently, the status of a new species of atyid shrimp from Pohnpei (Micronesia) was discussed in relation to C. brachydactyla De Man, 1908 and C. mertoni J. Roux, 1911. By combining morphological data with a phylogenetic analysis with closely related species, this species is here described as Caridina variabilirostris sp. nov. Notes on its ecological distribution are also provided. The new species is characterized by a highly variable rostrum and is present in rivers all over Pohnpei Island. The status of this new species is clarified and it is shown that neither C. brachydactyla De Man 1908 nor C. mertoni J. Roux, 1911 occur on Pohnpei Island.