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We report here the results from two field trips to collect Odonata in the Crocker Range National Park in western Sabah, Borneo, Malaysia. Thirtysix species were collected. Telosticta fugispinosa had not been described at the time of collection, nor had the two Devadatta species. There was no published record of Protosticta species cf kinabaluensis before the 2012 expedition, nor of Drepanosticta species cf crenitis.
Daddy-long-leg giants: revision of the spider genus Artema Walckenaer, 1837 (Araneae, Pholcidae)
(2017)
This is the first revision of Artema Walckenaer, 1837, a genus consisting of large and phylogenetically interesting species. Even though Artema is not species-rich (now eight nominal species), it has suffered from poor descriptions and synonymies. Our main goal was to gather all available material and to clarify species limits. Four species are easily distinguished from other congeners: Artema atlanta Walckenaer, 1837, the type species; A. kochi Kulczyński, 1901 (revalidated); A. bunkpurugu Huber & Kwapong, 2013; and A. nephilit sp. nov. All other species are problematic for varying reasons: species limits are unclear between A. doriae Thorell, 1881 and A. transcaspica Spassky, 1934; A. magna Roewer, 1960 and A. ziaretana (Roewer, 1960) are problematic because they are based on female and juvenile types respectively and little new material is available. The material available to us suggests the existence of a few further species; however, they are not formally described, either because of small sample sizes (Artema sp. a and A. sp. b are represented by only one specimen each) or because of unclear species limits (between Artema sp. c, A. transcaspica and A. doriae).This study is the first serious step towards understanding the genus. Intensive collecting effort is needed in order to fully clarify species limits.
In this work we present a revision of the genus Ommatoiulus Latzel, 1884 in Portugal. Based on recently collected material and older museum samples, including type specimens, we describe six new species to science, viz. Ommatoiulus alacygni sp. nov., O. camurus sp. nov., O. denticulatus sp. nov., O. litoralis sp. nov., O. staglae sp. nov. and O. stellaris sp. nov. The species O. alacygni sp. nov., O. denticulatus sp. nov. and O. staglae sp. nov. described from the Algarve are outstanding by their extremely reduced mesomerital process. The species O. porathi (Verhoeff, 1893) and O. andalusius (Attems, 1927) are recorded and redescribed for the first time after their original description. The finding of O. andalusius – originally described from Andalusia in Spain – constitutes a new record for Portugal together with two species, viz. O. fuentei (Brolemann, 1920) and O. martensi Mauriès, 1969. The taxonomic status of several species is revised. Thus Archiulus (Schistocoxitus) cingulatus Attems, 1927 is here considered as a junior synonym of Ommatoiulus lusitanus (Verhoeff, 1895) while Schizophyllum cervinum Verhoeff, 1910 is synonymized with Ommatoiulus moreleti (Lucas, 1860). An identification key to all hitherto known Portuguese species of Ommatoiulus is presented as well as a distribution map illustrating the various species occurrences in the country.
Keys and diagnoses of North European aphids (Hemiptera, Aphidoidea) feeding on conifers are given, including species from nearby areas of Central and Western Europe, based on live and freeze-dried material. Externally visible informative characters, such as body shape, colours, wax coating, and pigmentation pattern are utilized, in addition to characters traditionally used in the literature. Rich illustrations with photographs of live colonies and freeze-dried specimens, supported by drawings where needed, are presented. The combination of colour images and diagnoses, utilizing easily observed characters, allows the identification of a large number of species already in the field, and many more at home with the aid of a stereo microscope. Host plant relationships and aphid-ant associations are presented.
The Middle East biting midges of the tribes Palpomyiini (20 species in three genera) and Sphaeromiini s. lat. (six species in five genera) are reviewed. Three new species are described and illustrated: Bezzia libanensis Alwin & Szadziewski sp. nov., B. sharjahi Alwin & Szadziewski sp. nov. and Palpomyia freidbergi Alwin & Szadziewski sp. nov. Bezzia aegyptia Kieffer, 1925 is recognized as a new junior synonym of B. albicornis (Meigen, 1818) (syn. nov.) and B. omanensis Boorman & van Harten, 2002, is recognized as a junior synonym of B. (Sivabezzia) pachypyga Remm, 1974 (syn. nov.). Keys to the genera and species of the tribes Palpomyiini and Sphaeromiini of the Middle East are also provided.
The Republic of Panama currently has 21 recorded species of stoneflies, all in the genus Anacroneuria (Plecoptera: Perlidae). Herein, we record five species of this genus from the Mount Totumas Cloud Forest and Biological Reserve, in the upper reaches of the Río Chiriquí Viejo watershed. One of these species, A. plutonis (Banks), represents a new country record for Panama. These results are part of an ongoing effort to characterize the aquatic insect fauna of Panama, and to evaluate that country’s major watersheds.
Polychelidan lobsters (Decapoda: Polychelida) are crustaceans with extant species which are restricted to deep water environments. Fossil species, however, used to live in more varied palaeoenvironments, from shallow water to deep water, and were more diverse morphologically. We redescribe two species of polychelidan lobsters, the Late Triassic Rosenfeldia triasica Garassino, Teruzzi & Dalla Vecchia, 1996 and the Late Jurassic Eryon oppeli Woodward, 1866, recently assigned to the same genus, Rosenfeldia, based upon only a few characters. Our investigation of all available material of both species leads us to distinguish these two species and to erect Rogeryon gen. nov. to accommodate Eryon oppeli. The palaeobiology of both species is interpreted for the first time. Rosenfeldia triasica with its stout first pereiopods and mandibles with both incisor and molar processes (documented for the first time in Polychelida) was benthic and probably fed either on slow-moving sedentary preys or was a scavenger. Rogeryon oppeli gen. et comb. nov. was benthic, visually adapted to shallow water palaeoenvironments, and possibly had a diet similar to that of slipper lobsters and horseshoe crabs. The redescription of these two species highlights the palaeobiological diversity of fossil polychelidans.
We describe a new vanilla species growing in sympatry with Vanilla planifolia Jacks. ex Andrews (Orchidaceae) in the province of Limón, Caribbean coast of Costa Rica. The morphology of the reproductive and vegetative organs observed on vines cultivated under shade-house, the nuclear (Internal Transcribed Spacer) and plastid (matK) nucleotide sequences, as well as the contents of aromatic compounds measured in ripe fruits, show that this species is close to but distinct from V. planifolia. The name V. sotoarenasii M.Pignal, Azofeifa-Bolaños & Grisoni sp. nov. is proposed for this new Vanilla species endemic in Costa Rica. It is especially distinguished from V. planifolia by a reduction of about 30% of the size of the fruits and flowers, by a divergence of ITS sequences for at least two species-conserved nucleotides compared to seven other species of the V. planifolia group, and by the presence of anisic compounds and low content of phenolic compounds (including vanillin) in the fruits. These results confirmed the extension of the area of distribution of V. planifolia southward to Costa Rica, where a recent speciation process occurred. Because of its particular agronomic and aromatic properties, V. sotoarenasii sp. nov. could represent a valuable biological resource for the vanilla industry.
Cnestus mutilatus (Blandford) (Coleoptera: Curculionidae: Scolytinae) is reported from Pennsylvania for the fi rst time, new state record. Specimens were collected using baited Lindgren funnels as early as 2013. Within Pennsylvania, C. mutilatus is now reported from Berks, Bucks, Lehigh, Montgomery, and York Counties.
Cixidia fusca and Synecdoche impunctata (Hemiptera: Achilidae) are reported from Missouri for the first time, new state records. Ecological and trapping information is also provided.
The fouling serpulids (Polychaeta: Serpulidae) from United States coastal waters: an overview
(2017)
Serpulids are an important component of fouling communities. This paper provides an overview of the serpulid species found in North America, as part of a broader study of fouling invertebrates focused on NIS (non-indigenous species) in United States coastal ecosystems. Almost 4400 serpulid specimens were examined from selected fouling plates. Fouling plates were deployed in 26 bays and coastal lagoons along the continental coasts of the United States and Hawaiian islands, primarily in bays and lagoons with salinities averaging 20‰ or greater. Twenty-five serpulid species were identified, including four new records for the United States (Ficopomatus uschakovi, Hydroides cf. brachyacantha, H. longispinosa and Protula longiseta), three known NIS, two presumed NIS, three cryptogenic serpulids, and several range extensions. Crucigera websteri extends its northward range from Santa Barbara Island to Humboldt Bay, California; Ficopomatus enigmaticus, first recorded in North America from San Francisco, California in 1920, Rockport, Texas in 1952 and Barnegat Bay, New Jersey in 1980, is now recorded at additional localities on the east coast (Chesapeake Bay, Virginia, Charleston, South Carolina and Indian River, Florida) and the northern Gulf of Mexico (Galveston Bay, Texas); F. miamiensis extends its westward range from Louisiana to Texas; F. uschakovi, an Indo-Pacific and Western African species, was recorded formally for the first time from the northern Gulf of Mexico ((Galveston Bay and Corpus Christi, Texas) and the east coast of Florida (Jacksonville). Hydroides cf. brachyacantha extends its northward range from Curaҫao to Pensacola Bay, Florida; H. dirampha from Veracruz, Mexico to Corpus Christi, Texas; H. floridana extends its westward range from Louisiana to Texas; H. gracilis extends its northward range from Pacific Grove to San Francisco, California; Salmacina huxleyi from Cape Hatteras, North Carolina to Rhode Island; and Spirobranchus minutus from Veracruz, Mexico to Pensacola Bay, Florida. The following additional species range extensions are provisional in that they represent only one record or were not found in the most recent surveys (e.g., Hydroides elegans - east coast): H. longispinosa from Marshall Islands to Oahu, Hawaii; Protula balboensis from Florida to Texas; P. longiseta from the Mexican Caribbean to the Indian River, Florida; H. elegans from San Francisco to Humboldt Bay, northern California and on the east coast from the Indian River, Florida, to Cape Cod, Massachusetts. Among surveyed bays, Biscayne Bay, Florida and Corpus Christi, Texas (northern Gulf of Mexico) had the greatest number of species (14 and 8, respectively); in contrast, almost all sites in Alaska, Washington, Oregon (northwest Pacific), Rhode Island, Virginia and South Carolina (Atlantic) had only one or two species each. Hydroides dianthus was, by far, the most abundant serpulid species on fouling plates in the northern Gulf of Mexico and the east coast, while Pseudochitinopoma occidentalis was the most abundant serpulid detected on the west coast. For each species recorded herein, we include the synonyms and some key references, a material studied section, a diagnosis, and updated distributional information. A checklist and identification key to the known shallow-water serpulids sensu stricto of the United States are included.
Ten new species belonging to three new genera (Atlantisina gen. nov., Bathycyclopora gen. nov., Calvetopora gen. nov.) of umbonulomorph bryozoans from northeastern Atlantic seamounts, islands, and the continental slope are introduced. We furthermore erect the new family Atlantisinidae fam. nov. for these genera. Eight new species belong to the new genus Atlantisina: Atlantisina atlantis gen. et sp. nov. (type species), A. acantha gen. et sp. nov., A. gorringensis gen. et sp. nov., A. inarmata gen. et sp. nov., A. lionensis gen. et sp. nov., A. meteor gen. et sp. nov., A. seinensis gen. et sp. nov., and A. tricornis gen. et sp. nov. The genus Bathycyclopora gen. nov. is introduced for ?Phylactella vibraculata Calvet from the Azores, and also includes Bathycyclopora suroiti gen. et sp. nov. The type species of Calvetopora gen. nov. is Lepralia inflata Calvet from the Gulf of Cadiz; this genus also includes Calvetopora otapostasis gen. et sp. nov. and another species left in open nomenclature. Of the 13 species described herein, 11 occur on seamounts and islands, and nine species are endemic to a single seamount, island or station. The present results show that bryozoans provide striking examples of the function of seamounts as areas of endemism, most likely intrinsically linked to the low dispersal abilities of bryozoan larvae.
Species of Mortoniella are revised for the northern and Andean part of the South American continent, including the countries of Bolivia, Peru, Ecuador, Colombia, Venezuela, and Guyana. All previously described species from the region are reillustrated and redescribed, except for Mortoniella santiaga Sykora, 1999 and M. quinuas Harper and Turcotte, 1985, whose types could not be located, and M. tranquilla Martynov, 1912, whose type is based on a female specimen and thus is currently unidentifiable. Included in the revision are 35 described species and 59 new species. Mortoniella similis Sykora, 1999 is considered a junior synonym of M. roldani Flint, 1991, and M. macuta (Botosaneanu, 1998) is considered a junior synonym of M. limona (Flint, 1981). A new subgenus, Nanotrichia, is recognized to accommodate species previously referred to as members of the ormina and velasquezi groups. Mexitrichia pacuara Flint, 1974 is designated the type species for the subgenus. Species previously referred to as members of the bilineata and leroda species groups are retained in the nominate subgenus, along with additional taxa not previously placed to species group, and treated within a number of subgroups. Previously described species of M. (Mortoniella) which are redescribed and reillustrated include: M. angulata Flint, 1963; M. apiculata Flint, 1963; M. atenuata (Flint, 1963); M. bifurcata Sykora, 1999; M. bilineata Ulmer, 1906; M. bolivica (Schmid, 1958); M. chicana Sykora, 1999; M. denticulata Sykora, 1999; M. elongata (Flint, 1963); M. enchrysa Flint, 1991; M. flinti Sykora, 1999; M. foersteri (Schmid, 1964); M. hodgesi Flint, 1963; M. iridescens Flint, 1991; M. leei (Flint, 1974); M. limona (Flint, 1981); M. marini (Rueda Martín and Gibon, 2008); M. paralineata Sykora, 1999; M. paraenchrysa Sykora, 1999; M. pocita (Flint, 1983); M. punensis (Flint, 1983); M. roldani Flint, 1991; M. simla (Flint, 1974); M. spinulata (Flint, 1991); M. squamata Sykora, 1999; M. unilineata Sykora, 1999; and M. wygodzinskii (Schmid, 1958). New species described in M. (Mortoniella), followed by their respective areas of distribution, include: M. acutiterga (Ecuador); M. adamsae (Peru); M. akrogeneios (Ecuador); M. applanata (Peru); M. auricularis (Colombia); M. barinasi (Venezuela); M. biramosa (Venezuela); M. bothrops (Peru); M. brevis (Ecuador, Venezuela); M. bulbosa (Peru); M. catherinae (Peru); M. chalalan (Peru); M. cornuta (Peru); M. cressae (Venezuela); M. croca (Peru); M. curtispina (Venezuela); M. curvistylus (Ecuador); M. dentiterga (Ecuador); M. dinotes (Peru); M. draconis (Ecuador); M. emarginata (Ecuador, Colombia); M. esrossi (Colombia); M. flexuosa (Colombia); M. furcula (Ecuador); M. gilli (Ecuador); M. gracilis (Venezuela); M. grandiloba (Venezuela); M. guyanensis (Guyana); M. hamata (Colombia); M. langleyae (Ecuador); M. longiterga (Ecuador); M. membranacea (Bolivia); M. monopodis (Colombia, Ecuador); M. parameralda (Ecuador); M. pica (Ecuador); M. proakantha (Ecuador); M. prolata (Peru); M. quadrispina (Ecuador); M. rectiflexa (Ecuador); M. ruedae (Bolivia); M. schlingeri (Colombia); M. silacea (Colombia, Ecuador); M. sinuosa (Bolivia, Peru); M. spatulata (Venezuela); M. tanyrhabdos (Venezuela); M. tridens (Peru); M. triramosa (Bolivia); M. tusci (Venezuela); and M. variabilis (Venezuela, Colombia). Species assigned to the subgenus M. (Nanotrichia) which are redescribed and reillustrated include: M. aequalis (Flint, 1963); M. aries (Flint, 1963); M. collegarum (Rueda Martín and Gibon, 2008); M. eduardoi (Rueda Martín and Gibon, 2008); M. macarenica (Flint, 1974); M. pacuara (Flint, 1974); M. usseglioi (Rueda Martín and Gibon, 2008); and M. velasquezi (Flint, 1991). Previously described species of Mortoniella, outside the area of coverage, that are transferred to the subgenus M. (Nanotrichia) include: M. alicula Blahnik and Holzenthal, 2011; M. bocaina Blahnik and Holzenthal, 2011; M. catarinensis (Flint, 1974); M. froehlichi Blahnik and Holzenthal, 2011; M. ormina (Mosely, 1939); M. rodmani Blahnik and Holzenthal, 2008; and M. tripuiensis Blahnik and Holzenthal, 2011. New species in the subgenus M. (Nanotrichia), followed by their respective areas of distribution, include: Mortoniella cognata (Ecuador, Venezuela); M. coheni (Ecuador); M. licina (Ecuador); M. paucispina (Peru); M. quadridactyla (Venezuela); M. simplicis (Venezuela); M. spangleri (Ecuador); M. triangularis (Ecuador); M. venezuelensis (Venezuela); and M. zamora (Ecuador). A key to the males of species from the region is also provided, as well as a key to females for the major subgroups and a species key to females of the velasquezi group. Finally, a partially resolved phylogeny of the species is presented, along with a discussion of evolutionary trends within the genus.
Species of Mortoniella are revised for the northern and Andean part of the South American continent, including the countries of Bolivia, Peru, Ecuador, Colombia, Venezuela, and Guyana. All previously described species from the region are reillustrated and redescribed, except for Mortoniella santiaga Sykora, 1999 and M. quinuas Harper and Turcotte, 1985, whose types could not be located, and M. tranquilla Martynov, 1912, whose type is based on a female specimen and thus is currently unidentifiable. Included in the revision are 35 described species and 59 new species. Mortoniella similis Sykora, 1999 is considered a junior synonym of M. roldani Flint, 1991, and M. macuta (Botosaneanu, 1998) is considered a junior synonym of M. limona (Flint, 1981). A new subgenus, Nanotrichia, is recognized to accommodate species previously referred to as members of the ormina and velasquezi groups. Mexitrichia pacuara Flint, 1974 is designated the type species for the subgenus. Species previously referred to as members of the bilineata and leroda species groups are retained in the nominate subgenus, along with additional taxa not previously placed to species group, and treated within a number of subgroups. Previously described species of M. (Mortoniella) which are redescribed and reillustrated include: M. angulata Flint, 1963; M. apiculata Flint, 1963; M. atenuata (Flint, 1963); M. bifurcata Sykora, 1999; M. bilineata Ulmer, 1906; M. bolivica (Schmid, 1958); M. chicana Sykora, 1999; M. denticulata Sykora, 1999; M. elongata (Flint, 1963); M. enchrysa Flint, 1991; M. flinti Sykora, 1999; M. foersteri (Schmid, 1964); M. hodgesi Flint, 1963; M. iridescens Flint, 1991; M. leei (Flint, 1974); M. limona (Flint, 1981); M. marini (Rueda Martín and Gibon, 2008); M. paralineata Sykora, 1999; M. paraenchrysa Sykora, 1999; M. pocita (Flint, 1983); M. punensis (Flint, 1983); M. roldani Flint, 1991; M. simla (Flint, 1974); M. spinulata (Flint, 1991); M. squamata Sykora, 1999; M. unilineata Sykora, 1999; and M. wygodzinskii (Schmid, 1958). New species described in M. (Mortoniella), followed by their respective areas of distribution, include: M. acutiterga (Ecuador); M. adamsae (Peru); M. akrogeneios (Ecuador); M. applanata (Peru); M. auricularis (Colombia); M. barinasi (Venezuela); M. biramosa (Venezuela); M. bothrops (Peru); M. brevis (Ecuador, Venezuela); M. bulbosa (Peru); M. catherinae (Peru); M. chalalan (Peru); M. cornuta (Peru); M. cressae (Venezuela); M. croca (Peru); M. curtispina (Venezuela); M. curvistylus (Ecuador); M. dentiterga (Ecuador); M. dinotes (Peru); M. draconis (Ecuador); M. emarginata (Ecuador, Colombia); M. esrossi (Colombia); M. flexuosa (Colombia); M. furcula (Ecuador); M. gilli (Ecuador); M. gracilis (Venezuela); M. grandiloba (Venezuela); M. guyanensis (Guyana); M. hamata (Colombia); M. langleyae (Ecuador); M. longiterga (Ecuador); M. membranacea (Bolivia); M. monopodis (Colombia, Ecuador); M. parameralda (Ecuador); M. pica (Ecuador); M. proakantha (Ecuador); M. prolata (Peru); M. quadrispina (Ecuador); M. rectiflexa (Ecuador); M. ruedae (Bolivia); M. schlingeri (Colombia); M. silacea (Colombia, Ecuador); M. sinuosa (Bolivia, Peru); M. spatulata (Venezuela); M. tanyrhabdos (Venezuela); M. tridens (Peru); M. triramosa (Bolivia); M. tusci (Venezuela); and M. variabilis (Venezuela, Colombia). Species assigned to the subgenus M. (Nanotrichia) which are redescribed and reillustrated include: M. aequalis (Flint, 1963); M. aries (Flint, 1963); M. collegarum (Rueda Martín and Gibon, 2008); M. eduardoi (Rueda Martín and Gibon, 2008); M. macarenica (Flint, 1974); M. pacuara (Flint, 1974); M. usseglioi (Rueda Martín and Gibon, 2008); and M. velasquezi (Flint, 1991). Previously described species of Mortoniella, outside the area of coverage, that are transferred to the subgenus M. (Nanotrichia) include: M. alicula Blahnik and Holzenthal, 2011; M. bocaina Blahnik and Holzenthal, 2011; M. catarinensis (Flint, 1974); M. froehlichi Blahnik and Holzenthal, 2011; M. ormina (Mosely, 1939); M. rodmani Blahnik and Holzenthal, 2008; and M. tripuiensis Blahnik and Holzenthal, 2011. New species in the subgenus M. (Nanotrichia), followed by their respective areas of distribution, include: Mortoniella cognata (Ecuador, Venezuela); M. coheni (Ecuador); M. licina (Ecuador); M. paucispina (Peru); M. quadridactyla (Venezuela); M. simplicis (Venezuela); M. spangleri (Ecuador); M. triangularis (Ecuador); M. venezuelensis (Venezuela); and M. zamora (Ecuador). A key to the males of species from the region is also provided, as well as a key to females for the major subgroups and a species key to females of the velasquezi group. Finally, a partially resolved phylogeny of the species is presented, along with a discussion of evolutionary trends within the genus.
Big and beautiful: the Megaxyela species (Hymenoptera, Xyelidae) of East Asia and North America
(2017)
Megaxyela Ashmead, 1898 comprises 13 species, four of which are described as new and one is removed from synonymy: Megaxyela euchroma Blank, Shinohara & Wei sp. nov. from China (Zheijang), M. fulvago Blank, Shinohara & Wei sp. nov. from China (Hunan, Jiangsu, Zhejiang), M. inversa Blank & D.R. Smith sp. nov. from the USA (West Virginia), M. langstoni Ross, 1936 sp. rev. from the eastern USA, and M. pulchra Blank, Shinohara & Sundukov sp. nov. from China (Hubei, Jilin, Liaoning, Shaanxi, Tibet), South Korea (Kangwon-do) and Russia (Primorskiy Kray). The male of M. parki Shinohara, 1992 is described for the first time. A lectotype is designated for M. gigantea Mocsáry, 1909. A cladogram, based on COI sequences of seven species, is presented and interpreted in view of selected morphological characters. Records of M. fulvago sp. nov. from Hunan and of M. pulchra sp. nov. from Tibet extend the known distribution of Megaxyela in the Old World 600 kilometers farther south and 2500 kilometers farther west than previous records.
A detailed study of the holotype of Sphecomyrma canadensis Wilson, 1985 (Hymenoptera: Formicidae) from Canadian amber has led to the conclusion that the specimen belongs to a new genus, here named Boltonimecia gen.n. Since the taxonomy of stem-group ants is not well understood, in order to find the taxonomic position of this genus, it is necessary to review the classifi cation of stem-group ants in a study of their relation to crown-group ants. In the absence of data for traditional taxonomic approaches, a statistical study was done based on a morphometric analysis of antennae. Scape elongation is believed to play an important role in the evolution of eusociality in ants; however, this hypothesis has never been confirmed statistically. The statistical analysis presented herein lends support to the view that antennal morphology reliably distinguishes stem-group ants from crown-group ants, to determine whether a species belongs to one or the other group. This, in turn, may indicate a relationship exists between eusociality and scape elongation. A review of Cretaceous records of ants is made and the higher classification of Formicidae with definitions of stem and crown groups is proposed. Newly obtained data are discussed focusing particularly on the origin, evolution and diversity of ants.
Loxosceles Heineken & Lowe, 1832 spiders are infamous for their medical importance, but a taxonomic picture of the genus is still far from complete. In this study, the Chilean species of Loxosceles are described and mapped. The males of Loxosceles surca Gertsch, 1967 and L. coquimbo Gertsch, 1967 are described for the first time. Three new species with narrow distributions are described from central and northern Chile: Loxosceles diaguita sp. nov. from the Antofagasta Region, L. pallalla sp. nov. from Coquimbo and L. vallenar sp. nov. from Atacama. The first two species are remarkable in their morphology and do not fit into any of Gertsch’s species groups, suggesting that Chile still harbours an undiscovered phylogenetic diversity of the genus. New distribution records for Loxosceles laeta (Nicolet, 1849) are provided throughout Chile.
The genus Otraleus Günther, 1935 is recorded from the Philippines for the first time. Four new species, Otraleus bellemansae sp. nov., O. applai sp. nov., O. christianae sp. nov. and O. elizabethae sp. nov., are described from the highlands of Northwestern Luzon. The characters allowing separation from O. hypsimelathrus Günther, 1935 and O. labanrataensis Soew-Choen, 2016, are given. A new genus closely related to Otraleus, Capuyanus gen. nov., is described with a single species, C. magwilangi sp. nov., as type-species. An identification key and distribution maps are provided for all species.
This paper deals with the taxonomy and faunistics of the genus Diplommatina in Nepal. Altogether 16 species are reported, seven of which are new to science viz. D. abiesiana sp. nov., D. fistulata sp. nov., D. godawariensis sp. nov., D. maipokhariensis sp. nov., D. salgharica sp. nov., D. shivapuriensis sp. nov. and D. syabrubesiensis sp. nov. Information on nine previously reported species is provided: D. exserta Godwin-Austen, 1886, D. folliculus (L. Pfeiffer, 1846), D. miriensis Godwin-Austen, 1917, D. munipurensis Godwin-Austen, 1892, D. oviformis Fulton, 1901, D. pachycheilus Benson, 1857, D. regularis Fulton, 1901, D. silvicola Godwin-Austen, 1886 and D. sperata W.T. Blanford, 1862. Although D. canarica was once reported from Nepal, it is not treated here as it is an endemic of the Western Ghats. A dichotomous identification key for all Nepalese species is presented.
Contributions to the knowledge of the mite genus Stigmaeus Koch, 1836 (Acari: Stigmaeidae) of Turkey
(2017)
Based on the mite specimens collected within the scope of a study on Erzincan (Turkey) mite biodiversity, two species of the genus Stigmaeus are described and illustrated here: S. bifurcus sp. nov. as new to science and S. miandoabiensis Bagheri & Zarei, 2012 as a new record for Turkey. Some morphological abnormalities in the new species are noted. The deutonymph of S. miandoabiensis is described for the first time in this study. Discovery of this stage from soil and litter under Pinus sylvestris in Turkey adds more data to our knowledge of the species.
To date, six species of the Australian endemic millipede genus Boreohesperus have been recognized: all have highly localized distributions, consistent with being short-range endemic species, and all are from the Cape Range and Pilbara region of Western Australia. In this paper, we describe three new species, B. alcyonis sp. nov., B. psittacinus sp. nov., and B. vascellus sp. nov., each from a different island in the Kimberley region of north-western Australia.
Macrobrachium australe is an amphidromous prawn living in the insular freshwater systems of the Indo-Pacific. Because it possesses few informative morphological characters, that often vary from one habitat to another, M. australe has produced much taxonomic confusion and has historically been described under eight synonyms. Here, 53 specimens collected throughout the Indo-Pacific under the name M. australe were phylogenetically and morphologically examined. Results revealed that what has been called M. australe belongs to at least two distinct species: M. australe, distributed from the Southwest Indian Ocean to the Central Pacific Ocean, and a cryptic species potentially restricted to the Northwest Pacific Ocean, here identified as M. ustulatum, which until now was considered as a junior synonym. Although they are not quite found in the same habitat (lentic-lotic), the presence of these distinct, and reciprocally monophyletic entities in the same rivers on the islands of Palau and Santo strongly favors the hypothesis of two reproductively isolated entities. Six morphological characters, including the proportions of the joints of the male second pereiopod, the shape of the epistome lobe and the armature of the fourth thoracic sternite, are evidenced as diagnostic. A neotype of M. australe is designated and deposited in the Muséum national d’Histoire naturelle in Paris.
In shelled molluscs, assigning valid species names to independent evolutionary lineages can be a difficult task. Most original descriptions are based on empty shells and the high levels of variation in shape, color and pattern in some groups can make the shell a poor proxy for species-level identification. The deep-sea gastropod turbinid genus Bolma is one such example, where species-level identification based on shell characters alone is challenging. Here, we show that in Bolma both traditional and molecular taxonomic treatments are associated with a number of pitfalls that can lead to biased inferences about species diversity. Challenges derive from the few phylogenetically informative characters of shells, insufficient information provided in original descriptions and sampling artefacts, which at the molecular level in spatially fragmented organisms can blur distinctions between genetically divergent populations and separate species. Based on a comprehensive dataset combining molecular, morphological and distributional data, this study identified several cases of shell-morphological plasticity and convergence. Results also suggest that what was thought to be a set of distinct, range-restricted species corresponds instead to a smaller number of more widespread species. Overall, using an appropriate sampling design, including type localities, allowed us to assign available names to evolutionarily significant units.
Five species of the terrestrial diatom genus Luticola D.G.Mann were found during a taxonomic survey of two small volcanic islands, Ile Amsterdam and Ile Saint-Paul (Southern Indian Ocean). Apart from the two already known Luticola species L. beyensii Van de Vijver et al. and L. subcrozetensis Van de Vijver et al., two new species are described: L. ivetana Chattová & Van de Vijver sp. nov. and L. vancampiana Chattová & Van de Vijver sp. nov. Finally, one, up to now unknown, Luticola species is briefly discussed and illustrated. Detailed morphological descriptions of these taxa are provided based on both light and scanning electron microscopy observations. Morphological features of the new species are compared to morphologically similar taxa, and notes on their ecology and biogeography are added.
New records of Odonata from Kelantan, Malaysia, with a checklist of species recorded from the state
(2017)
We report here the results from field trips to collect Odonata in the central and northeastern parts of Kelantan state, Peninsular Malaysia. Sixty eight species were collected, and 15 of these are new records for the state. Interesting species collected include Euphaea masoni Selys, 1879 and Leptogomphus tioman Choong, 2016. A checklist of the Odonata recorded from Kelantan with a total 131 confirmed species is given in an appendix.
For much of the last thirty years, the caesalpinioid genus Bauhinia has been recognised by numerous authors as a broadly circumscribed, ecologically, morphologically and palynologically diverse pantropical taxon, comprising several subgenera. One of these, Bauhinia subg. Phanera has recently been reinstated at generic rank based on a synthesis of morphological and molecular data. Nevertheless, there remains considerable diversity within Phanera. Following a review of palynological and molecular studies of Phanera in conjunction with a careful re-examination of the morphological heterogeneity within the genus, we have found strong evidence that the species of Phanera subsect. Corymbosae are a natural group that warrant generic status. We describe here the genus Cheniella R.Clark & Mackinder gen. nov. to accommodate them. It comprises 10 species and 3 subspecies, one newly described here. Generic characters include leaves that are simple and emarginate or bilobed; flowers with elongate hypanthia which are as long as or much longer than the sepals; pods that are glabrous, compressed, oblong, indehiscent or tardily dehiscent; and with numerous seeds, the seeds bearing an unusually long funicle extending most of the way around their circumference. A further distinctive floral character was found to be a fleshy disc on which the staminodes are mounted. An analysis carried out for this study reveals Cheniella to be characterised by a pollen type that is unique to the genus and previously unknown in the Leguminosae. Species diversity is richest in southern China, the full distribution extending westward to India and south- and eastward through Indochina into Malesia.
New Bolivian Rhinotragini (Coleoptera, Cerambycidae, Cerambycinae) are described: three species of Phygopoda Thomson, 1864 (P. longiscopifera sp. nov., P. boliviensis sp. nov. and P. chaquensis sp. nov.); and one species of Phygopoides Peñaherrera-Leiva and Tavakilian, 2007 (P. maxwelli sp. nov.). Two Brazilian species of Neophygopoda Melzer, 1933 are transferred to the genus Phygopoda: P. exilis (Melzer, 1933) comb. nov. and P. agdae (Martins, Galileo and Santos-Silva, 2015) comb. nov. All the species are illustrated, and a key to the Bolivian species of Phygopoda and host flower records are provided.
The taxonomic history of the rhinotragine genera Phygopoda Thomson, 1864 and Pseudophygopoda Tavakilian and Peñaherrera-Leiva, 2007 (Coleoptera: Cerambycidae: Cerambycinae) are discussed, and evidence is presented to suggest that some recent taxonomic changes made by Carelli and Monné (2015) were unjustified. Consequently, Phygopoda nigritarsis Gounelle, 1911 is moved to the genus Neophygopoda Melzer, 1933, creating the new combination Neophygopoda nigritarsis, the genera Panamapoda Clarke, 2014 and Paraphygopoda Clarke, 2014 are revalidated, and the species Paraphygopoda viridimicans (Fisher, 1952) and Paraphygopoda nappae Clarke, 2014 are also revalidated.
A preliminary catalogue of the moths (Lepidoptera except Papilionoidea) of Tobago, West Indies
(2017)
This catalogue comprises records of 355 species of moths (non-papilionoid Lepidoptera) from Tobago, of which 15 are partially identified. Of this total, all except 17 (5%) are known from Trinidad, although not all these records from Trinidad are published yet. Of these 17, eleven are expected to occur in Trinidad as they also occur on the mainland of South America and two are only known from Tobago but will probably also occur in Trinidad. This leaves just four species (1% of the total) that are known from the Lesser Antilles and are currently not known from further south than Tobago. The families represented by the most species are Erebidae, Crambidae, Geometridae, Noctuidae and Sphingidae, which between them account for 73% of records. Taxonomic changes are made as follows. Podalia farmbri (Kaye, 1925) sp. rev. (Megalopygidae) is removed from the synonymy of P. nigrescens Schaus, 1905. Podalia walkeri Hopp, 1935 and P. dimidiata (Walker, 1865) are syn. nov. of P. farmbri Kaye, 1925. Renia bipunctata (Kaye, 1901) (Erebidae) is a comb. nov. for Zanclognatha bipunctata. Aristaria trinitalis Schaus, 1906 (Erebidae) is a syn. nov. of Renia bipunctata Kaye, 1901. Aglaonice deldonalis Walker, 1859 sp. rev. (Erebidae) is removed from the synonymy of A. hirtipalpis Walker, [1859]. Plusiodonta cupristria Kaye, 1923 (Erebidae) is a syn. nov. of Oraesia excitans Walker [1858]. Oroscopa abluta (Schaus, 1912) (Erebidae) is a comb. nov. for Freilla abluta Schaus, 1912, which is a new combination in common use, but not previously published. Ptichodis dorsalis (Fabricius, 1797) (Erebidae) is a comb. nov. for Noctua auct. dorsalis Fabricius, a new combination already in use, but not formally published. I endorse the unpublished conclusion of I.W.B. Nye that Ptichodis basilans (Guenée, 1852) is a syn. nov. of Ptichodis dorsalis (Fabricius, 1797). Ptichodis agrapta Hampson, 1913 is also a syn. nov. of Ptichodis dorsalis (Fabricius, 1797).
Six annotated lists are presented: A, a checklist of the butterflies (Lepidoptera, Papilionoidea) of Tobago (150 species); B, species for which there are no records in the last 80 years (49 species); C, species needing confi rmation from Tobago (5 species); D, species not accepted from Tobago (12 species); E, species which are likely to occur in Tobago, but have not been recorded (6 species); and F, species and subspecies recorded from Tobago, but not from Trinidad (2 species and 2 subspecies). Remarkably, 33% of the 150 recorded species have not been reported
in the last 80 years. While it is possible that some of these are not resident or have become extinct, it seems more likely that most have simply not been found in the last 80 years. The butterfly fauna of Tobago merits further study; year-round collecting in different habitats and areas, using a variety of techniques, will surely fi ll in many of the apparent gaps in our knowledge. Ouleus fridericus sheldoni ssp. nov. (Hesperiidae, Pyrginae) is described from Tobago, with illustrations of adults and male genitalia, and is compared to O. fridericus sinepunctis (Kaye) from Trinidad. Danaus plexippus tobagi A.H. Clark, 1941 is a syn. nov. of D. plexippus nigrippus (Haensch, 1909) (Nymphalidae, Danainae).
Review of the clavatus group of the lanternfly genus Pyrops (Hemiptera: Fulgoromorpha: Fulgoridae)
(2017)
The clavatus group of Pyrops Spinola, 1839 is reviewed and redefined. The new combination Pyrops atroalbus (Distant, 1918) comb. nov. is proposed, as atroalbus is reinstated as a full species from status of subspecies of Pyrops watanabei (Matsumura, 1913). Pyrops nigripennis (Chou & Wang, 1985) and Pyrops clavatus mizunumai (Sato & Nagai, 1994) are proposed as junior synonyms of P. clavatus (Westwood, 1839). The Philippine species P. polillensis (Baker, 1925) is removed from the group and not attributed to any of the currently defined species groups. Hence, the clavatus group is restricted to continental Southeast Asia and Taiwan and contains three species: P. atroalbus comb. nov., P. clavatus and P. watanabei. A key to the species of the group and illustrations of the male genitalia are provided. The intraspecific colour variation in the group is discussed and illustrated. The genus Pyrops is removed from the subfamily Fulgorinae and not attributed to any of the currently defined subfamilies of Fulgoridae.
Two new species of the genus Gergithoides Schumacher, 1915 (Issinae, Hemisphaeriini), G. gnezdilovi sp. nov. from Bidoup-Nui Ba National Park in Central Vietnam and G. nui sp. nov. from Pia-Oac National Park in North Vietnam, are described. These are the only species of the genus formally recorded from Vietnam to date. Habitus, details and male genitalia are illustrated and a distribution map is provided. Four females representing three or four additional species, known from females only, are mentioned and illustrated. Taxonomic and biogeographical updates based on a thorough review of the literature are proposed and discussed for G. carinatifrons Schumacher, 1915, G. rugulosus (Melichar, 1906) and G. undulatus Wang & Che, 2003.
Three new species of Kynotus from the Central Highlands of Madagascar (Clitellata, Megadrili)
(2017)
The earthworm fauna of Madagascar is scarcely known. A recently launched exploration of the soil fauna (“Global Change and Soil Macrofauna Diversity in Madagascar”) resulted in the discovery of six new earthworm species belonging to the Malagasy endemic family Kynotidae. The success of the collecting campaign carried out between 2008 and 2011 inspired a new exploration of the earthworm fauna across the Central Highland Region of the island in the spring of 2015. During this expedition, two new species of Kynotus, K. ankisiranus sp. nov. and K. voimmanus sp. nov., were discovered. Barcoding of the recently collected species of Kynotus revealed that the unpigmented worms referred previously to K. alaotranus Michaelsen, 1897 also represented a new, still undescribed species, K. blancharti sp. nov.
Three new species of potamonautid freshwater crabs are described from the Lake Victoria region in southern Uganda, East Africa. Two of the new species (Potamonautes busungwe sp. nov. and P. entebbe sp. nov.) are from the shores of Lake Victoria, while the third (P. kantsyore sp. nov.) is from an inland locality on the Kagera River that flows into the lake. In addition, two of the new taxa (P. busungwe sp. nov. and P. kantsyore sp. nov.) are among the smallest species of freshwater crabs so far known from Africa. Diagnoses, illustrations and distribution maps are provided for these taxa, which are compared to similar species from Uganda and elsewhere in East Africa.
Epimeria of the Southern Ocean with notes on their relatives (Crustacea, Amphipoda, Eusiroidea)
(2017)
The present monograph includes general systematic considerations on the family Epimeriidae, a revision of the genus Epimeria Costa in Hope, 1851 in the Southern Ocean, and a shorter account on putatively related eusiroid taxa occurring in Antarctic and sub-Antarctic seas. The former epimeriid genera Actinacanthus Stebbing, 1888 and Paramphithoe Bruzelius, 1859 are transferred to other families, respectively to the Acanthonotozomellidae Coleman & J.L. Barnard, 1991 and the herein re-established Paramphithoidae G.O. Sars, 1883, so that only Epimeria and Uschakoviella Gurjanova, 1955 are retained within the Epimeriidae Boeck, 1871. The genera Apherusa Walker, 1891 and Halirages Boeck, 1891, which are phylogenetically close to Paramphithoe, are also transferred to the Paramphithoidae. The validity of the suborder Senticaudata Lowry & Myers, 2013, which conflicts with traditional and recent concepts of Eusiroidea Stebbing, 1888, is questioned. Eight subgenera are recognized for Antarctic and sub-Antarctic species of the genus Epimeria: Drakepimeria subgen. nov., Epimeriella K.H. Barnard, 1930, Hoplepimeria subgen. nov., Laevepimeria subgen. nov., Metepimeria Schellenberg, 1931, Pseudepimeria Chevreux, 1912, Subepimeria Bellan-Santini, 1972 and Urepimeria subgen. nov. The type subgenus Epimeria, as currently defined, does not occur in the Southern Ocean. Drakepimeria species are superficially similar to the type species of the genus Epimeria: E. cornigera (Fabricius, 1779), but they are phylogenetically unrelated and substantial morphological differences are obvious at a finer level. Twenty-seven new Antarctic Epimeria species are described herein: Epimeria (Drakepimeria) acanthochelon subgen. et sp. nov., E. (D.) anguloce subgen. et sp. nov., E. (D.) colemani subgen. et sp. nov., E. (D.) corbariae subgen. et sp. nov., E. (D.) cyrano subgen. et sp. nov., E. (D.) havermansiana subgen. et sp. nov., E. (D.) leukhoplites subgen. et sp. nov., E. (D.) loerzae subgen. et sp. nov., E. (D.) pandora subgen. et sp. nov., E. (D.) pyrodrakon subgen. et sp. nov., E. (D.) robertiana subgen. et sp. nov., Epimeria (Epimeriella) atalanta sp. nov., Epimeria (Hoplepimeria) cyphorachis subgen. et sp. nov., E. (H.) gargantua subgen. et sp. nov., E. (H.) linseae subgen. et sp. nov., E. (H.) quasimodo subgen. et sp. nov., E. (H.) xesta subgen. et sp. nov., Epimeria (Laevepimeria) anodon subgen. et sp. nov., E. (L.) cinderella subgen. et sp. nov., Epimeria (Pseudepimeria) amoenitas sp. nov., E. (P.) callista sp. nov., E. (P.) debroyeri sp. nov., E. (P.) kharieis sp. nov., Epimeria (Subepimeria) adeliae sp. nov., E. (S.) iota sp. nov., E. (S.) teres sp. nov. and E. (S.) urvillei sp. nov. The type specimens of E. (D.) macrodonta Walker, 1906, E. (D.) similis Chevreux, 1912, E. (H.) georgiana Schellenberg, 1931 and E. (H.) inermis Walker, 1903 are re-described and illustrated.
Distributional records of the 30 tiger beetle species and subspecies (Coleoptera: Carabidae: Cicindelinae) known for Brunei Darussalam are given together with habitus photos for 21 species. Neocollyris (Neocollyris) labiomaculata (Horn, 1892), Neocollyris (Neocollyris) emarginata (Dejean, 1825), Therates spectabilis fl avissimus Brouerius van Nidek, 1957, Heptodonta analis s. str. (Fabricius, 1801), Cosmodela velata (Bates, 1872), Lophyra (s. str.) fuliginosa (Dejean, 1826), Cylindera (Leptinomera) fi ligera (Bates, 1878), Myriochila (s. str.) specularis brevipennis (Horn, 1897), Abroscelis tenuipes araneipes (Schaum, 1863) and Callytron doriai (Horn, 1897) are reported for the fi rst time for the Sultanate.
DragonflyIndia Meet 2016
(2017)
The southeastern Australian millipede genus Pogonosternum Jeekel, 1965 is revised. Pogonosternum nigrovirgatum (Carl, 1902), P. adrianae Jeekel, 1982 and P. laetificum Jeekel, 1982 are redescribed; P. jeekeli Decker, sp. nov. and P. montanum Decker, sp. nov. are described from Victoria, New South Wales and Tasmania. P. nigrovirgatum infuscum Jeekel, 1982 and P. coniferum Jeekel, 1965 are junior synonyms of P. nigrovirgatum (Carl, 1902). An updated key to all five species of the genus is presented.
A systematic redefinition of the species belonging to the genus Geomyphilus Gordon and Skelley, 2007 (Coleoptera: Scarabaeidae: Aphodiinae) of Mexico and neighboring countries is presented. The new species G. tuzincola of Mexico is described and figured. The new combination Coelotrachelus macgregori (Islas, 1955) is proposed.
Three new fossil bryozoan species, a ctenostome and two cheilostomes, are described and figured from Pleistocene strata of the Wanganui Basin, New Zealand. Buskia waiinuensis sp. nov., a soft-body ctenostome preserved as a mould bioimmuration, is the first fossil record of the genus from New Zealand. Microporella rusti sp. nov., which is notable for the lack of ooecia in the large suite of colonies available, is one of the most common bryozoans in the Nukumaru Limestone and Nukumaru Brown Sand shellbeds, forming large encrusting sheet-like colonies, but is uncommon in younger beds. Rare, small-sized colonies of Parkermavella columnaris sp. nov. were found as fossil in two Quaternary beds, the Nukumaru Limestone and the Upper Kai-Iwi Shellbed, and also alive on rocks from greater Cook Strait area.
The monotypic Neotropical genus Ectophasiopsis Townsend, 1915 (Diptera, Tachinidae, Phasiinae) is revised, with the addition of two species (one new and another transferred species), and a redefinition of the genus, accompanied by photographs and drawings of specimens and male terminalia. A new combination is proposed, Ectophasiopsis gradata (Wiedemann, 1830) comb. nov., previously Trichopoda Berthold, 1827, and a new species Ectophasiopsis ypiranga sp. nov. is described. A key for the genera of the “Trichopoda typica” subgroup sensu Sabrosky (1950), as well as a key to species of Ectophasiopsis is given. The geographical range of the genus and the host list are updated.