Phylogeny of thrips (Insecta: Thysanoptera) based on five molecular loci

The order Thysanoptera (Paraneoptera), commonly known as thrips, displays a wide range of behaviours, and includes several pest species. The classification and suggested relationships among these insects remain morphologically based, and have never been evaluated formally with a comprehensive molecular phylogenetic analysis. We tested the monophyly of the suborders, included families and the recognized subfamilies, and investigated their relationships. Phylogenies were reconstructed based upon 5299 bp from five genetic loci: 18S ribosomal DNA, 28S ribosomal DNA, Histone 3, Tubulin‐alpha I and cytochrome oxidase c subunit I. Ninety‐nine thrips species from seven of the nine families, all six subfamilies and 70 genera were sequenced. Maximum parsimony, maximum likelihood and Bayesian analyses all strongly support a monophyletic Tubulifera and Terebrantia. The families Phlaeothripidae, Aeolothripidae, Melanthripidae and Thripidae are recovered as monophyletic. The relationship of Aeolothripidae and Merothripidae to the rest of Terebrantia is equivocal. Molecular data support previous suggestions that Aeolothripidae or Merothripidae could be a sister to the rest of Terebrantia. Four of the six subfamilies are recovered as monophyletic. The two largest subfamilies, Phlaeothripinae and Thripinae, are paraphyletic and require further study to understand their internal relationships.     

The genus Antillothrips Stannard, with descriptions of two new species (Thysanoptera: Phlaeothripidae)

Abstract. The genus Antillothrips Stannard ( Elatea Faure, syn.n.) is redefined with a key to the ten species: australis sp.n.; exastis (Ananthakrishnan & Kudo) stat.n. comb.n.; cingulatus (Hood) (= Haplothrips (Hindsiana) sakimurai Moulton syn.n.; Xenothrips opacus Ananthakrishnan & Kudo syn.n.); graminellus Ananthakrishnan & Jagadish; hartwigi sp.n.; malabaricus (Ananthakrishnan); micropterus Pitkin; nayari (Ananthakrishnan); stannmdi (Faure) comb.n.; varius (Ananthakrishnan & Jagadish). Lectotypes are designated for opacus and exastis.     

Modern thrips families Thripidae and Phlaeothripidae in Early Cretaceous amber (Insecta: Thysanoptera)

Two specimens of Thysanoptera with forked sensilla on third and fourth antennal segments were described from the Lebanese Neocomian and the Spanish Albian ambers, and attributed to the new genus Tethysthrips n. gen. in the family Thripidae Stevens 1829. One specimen with a tubular tenth abdominal segment was also discovered in the Lebanese Neocomian amber, and attributed to the new genus Rohrthrips n. gen. belonging to the family Phlaeothripidae Uzel 1895. Thripidae and Phlaeothripidae are nowadays the most species-rich families of Thysanoptera. The present discoveries of Early Cretaceous fossils show how diversified these families and thrips already were at that time. Moreover, this tubuliferan Rohrthrips specimen has plesiomorphies no longer present in the recent genera, in particular on the wings. Therefore it brings new insight in the evolution of Tubulifera.     

Species composition and structure of Thysanoptera communities in different microhabitats at the Parque Estadual de Itapu?, Viam?o, RS.

Although thrips are known as inhabitants of flowers, they are also abundant and diverse in other microhabitats. There is an information gap concerning them, especially related to the native fauna in southern Brazil. The structure and composition of the thysanopteran community in different microhabitats was studied at the "Parque Estadual de Itapu?" (30 degrees 22' S 51 degrees 02' W), RS, southern Brazil. Between June 1999 and May 2001, branches (n = 1,274), flowers (n = 774), grass tussocks (n = 596) and leaf litter (n = 603) were sampled systematically in 20 points of four trails (T1 - Pedreira beach, T2 - Ara?á beach, T3 - Lagoinha, and T4 - Grota hill). We found 2,197 adult thrips determined in 73 species in 41 genera, of which 37 could be nominated. Four families are represented, Thripidae, Phlaeothripidae, Heterothripidae and Merothripidae, with the first the most abundant (N = 1,599) and with the highest species richness (S = 32). The highest thrips abundance occurred in flowers N = 1,224 and the highest number of exclusive species occurred in the leaf litter (27). Frankliniella rodeos Moulton, 1933, Frankliniella gemina Bagnall, 1919 and Smicrothrips particula Hood, 1952 comprise 49.4% of the total sampled. Regarding T2, we obtained the highest abundance (N = 935) and highest species richness (S = 43). The composition of the faunas in each kind of environment proved very particular.     

Thysanoptera of the genus Dichromothrips on Old World Orchidaceae

Species of Dichromothrips are shown to be widespread on Orchidaceae in the Old World Tropics from Africa to New Zealand. The centre of diversity appears to be the Malaysian Region but this may be an artefact resulting from poor collections. The genus is redefined, its relationships discussed and a key provided to the 14 species [ australiae sp. nov., borneensis (Pr.); corbetti (Pr.); dendrobii Saki.; indicus sp. nov.; maori sp. nov._; nakahari sp. nov._; nigeriae sp. nov.; orchidis Pr.; phalaenopsidis Saki. (= sakimurai Bhatti syn.nov.); priesneri (Hood); semicognitus Saki.; smithi (Zimm.)j via torus sp. nov.|. Eugeneothrips Hood is synonymised with Dichromothrips.     

中国新记录属——梯背蓟马属记述（缨翅目：蓟马科)

记述中国缨翅目蓟马科1新记录属:梯背蓟马属Tenothrips Bhatti和1新记录种:变色梯背蓟马T. discolor (Karny, 1907)。研究标本保存在浙江大学昆虫研究所标本馆。     

Comprehensive phylogeny of the Cleroidea (Coleoptera: Cucujiformia)

The first thorough molecular phylogeny of the superfamily Cleroidea, represented by 377 taxa, and the first with an emphasis on Trogossitidae, was undertaken. Maximum likelihood and Bayesian analyses were performed on a four‐gene dataset (18S, 28S, cox1, cytb) of 395 taxa (along with 18 outgroups), including all 16 currently recognized families of Cleroidea and all current and formerly recognized tribes of Trogossitidae. The superfamily as a whole received strong support in Bayesian analyses. On the basis of phylogenetic results, 18 families in Cleroidea are recognized, including three taxa elevated to family for the first time and two reinstated families. The former tribe Rentoniini (Trogossitidae: Peltinae) was strongly supported as a monophyletic group apart from the remainder of Trogossitidae, and is herein elevated to family status, Rentoniidae stat.n. Protopeltis was also found to be an isolated lineage and becomes Protopeltidae stat.n. Peltini + Larinotini were recovered as a weakly supported sister grouping; Peltini (including only Peltis) becomes Peltidae stat.rest. The trogossitid subfamily Lophocaterinae, to the exclusion of Decamerini, formed a clade which is here designated Lophocateridae stat.rest. and sensu n. The Trogossitinae tribes Calityini, Egoliini (represented by Egolia) and Larinotini were recovered apart from core Trogossitidae but showed no strong affinities to other taxa or congruence between analyses; they are here conservatively retained in Trogossitidae as Calityinae stat.rest. , Egoliinae stat.rest. and Larinotinae stat.rest. The genus Thymalus of the peltine tribe Thymalini was indicated with moderate to strong support as the sister group of the Decamerini (Trogossitidae: Lophocaterinae); together these represent Thymalidae stat.n. and sensu n. with subfamilies Decamerinae stat.rest. ( new placement ) and Thymalinae stat.n. The remainder of Trogossitinae, the tribes Trogossitini and Gymnochilini, formed a well‐supported clade which comprises the Trogossitidae: Trogossitinae sensu n. The tribe Gymnochilini syn.n. is synonymized with Trogossitini. The monotypic family Phloiophilidae was recovered, contradicting a recent placement within Trogossitidae. The melyrid lineage was recovered with moderate (maximum likelihood) to strong (Bayesian analyses) support and includes the families Phycosecidae, Rhadalidae, Mauroniscidae, Prionoceridae and Melyridae (including Dasytidae and Malachiidae). The genus Dasyrhadus is tentatively transferred from Rhadalidae to Mauroniscidae. The genus Gietella, once proposed as a distinct family but recently placed within Dasytidae, was recovered as strongly sister to Rhadalidae sensu n. , and we transfer it to that family as Gietellinae new placement . Attalomiminae (formerly Attalomimidae) syn.n. is synonymized with Melyridae: Malachiinae: Lemphini sensu n. Melyridae sensu n. includes only Dasytinae, Malachiinae and Melyrinae. Metaxina is returned to the Chaetosomatidae sensu n. , of which Metaxinidae syn.n. becomes a junior synonym. Resolution within Cleridae was generally poor, but a broadly defined Korynetinae stat rest. + Epiclininae received high support (Bayesian analyses). Outside of Trogossitidae, the main focus of this study, major rearrangements of the classification of Cleroidea were not undertaken, despite evidence indicating such changes are needed.     

The West Indian species of Encyrtidae described by L. D. Howard, 1894 and 1897 (Hymenoptera, Chalcidoidea)

Abstract. The following species of encyrtids described by Howard (1894, 1897) from St Vincent and Grenada are redescribed or dealt with in some other way. The current generic placements and synonymies are indicated in parentheses. Archinus occupants (Archinus), Aphycus amoenus (Metaphycus comb.n.), Aratus scutellatus (= brasiliensis Subba Rao syn.n., Zeteticontus), Blastothrix insolitus ( Anagyrus comb .n. ), Bothriothorax insularis (Zeteticontus), Cerchysius terebratus (Anagyrus), Cerchysius pulchricornis (Anagyrus), Chieloneurus funiculus (= cupreicollis Ashmead syn.n., Cheiloneurus), Cheiloneurus nigrescens (= longisetaceus De Santis syn.n., Cheiloneurus), Copidosoma diversicomis (Apoanagyrus comb.n.), Encyrtus argentipes (Zaomma), Encyrtus crassus (= Encyrtus gargaris Walker syn.n. = Giraultella lopesi Costa Lima & Ferreira syn. n, Coelopencyrtus comb.n.), Encyrtus conformis (Encyrtus), Encyrtus convexus (= Encyrtus nitidus (Howard) syn. n.), Encyrtus flaviclavus (Encyrtus), Encyrtus hirtus (Hunterellus comb.n.), Encyrtus moderatus (= Adelencyrtus femoralis Compere & Annecke syn. n. = Adelencyrtus miyarai Tachikawa syn. n., Adelencyrtus comb.n.), Encyrtus nitidus (= Protyndarichus proximus De Santis syn. n., Protyndarichus comb.n.), Encyrtus quadricolor (Encyrtus), Encyrtus rotundiformis (Psyllaephagus comb.n.), Encyrtus sordidus (Forcipestricis comb.n.), Encyrtus submetallicus (Ooencyrtus), Habrolepoidea glauca (Habrolepoidea) and Homalopoda cristata (Homalopoda). Xiphomastix De Santis is synonymized with Anagyrus Howards (syn. n.), both included species ( X. nigriceps De Santis and X. bellator De Santis) being transferred to the latter. Propsyllaephagus Blanchard is synonymized with Psyllaephagus Ashmead (syn.n), Aratiscus laevigatus De Santis is transferred to Zeteticontus Silvestri (comb n.) and a key to the South American species of the genus is provided.     

The family and subfamily classification and New Zealand genera of Pythidae and Scraptiidae (Coleoptera)

ABSTRACT. The family Pythidae is defined on adult and larval characters to include the subfamilies Pythinae and PllipalPlnae. Trachelostenidae stat.n. is excluded. Relationships of Pythidae, Boridae, Trictenotomidae and SalPlngidae (s.l.) are analysed. Strong resemblances between some PllipalPlnae and Pyrochroidae appear to have arisen through convergent evolution. Adults and larvae of the New Zealand genera Techmessa, Techmessodes and Exocalopus are described. In Scraptiidae, adults of the New Zealand genera Nothotelus and Phytilea , and the larva of Nothotelus , are described. Type data are given for all described New Zealand species of these families. The following new synonymies are established: PllipalPlnae (Abdullah, 1964)=Techmessinae Paulus, 1971. Exocalopus pectinatus Broun, 1893= nitidiceps Broun, 1910. Techmessa concolor Bates, 1874= attenuata Broun, 1893= rugicollis Broun, 1910= unicolor Paulus, 1971. Techmessa telephoroides Bates, 1874= varians Broun, 1893. Techmessodes Plcticornis (Broun, 1880)= distans (Sharp, 1882). Techmessodes versicolor Broun, 1893= cephalotes Broun, 1910. The following genera are reassigned to the families indicated: Ischyomius to Trictenotomidae (from Pythidae or Melandryidae). Phytilea to Scraptiidae (from Oedemeridae or Anthicidae). Pseudananca to Aderidae (from Oedemeridae). Scraptogetus (= Metasclera ) to Aderidae (from Scraptiidae, Oedemeridae or Anthicidae).     

Rounding up the usual suspects: a standard target‐gene approach for resolving the interfamilial phylogenetic relationships of ecribellate orb‐weaving spiders with a new family‐rank classification (Araneae,Araneoidea)

We test the limits of the spider superfamily Araneoidea and reconstruct its interfamilial relationships using standard molecular markers. The taxon sample (363 terminals) comprises for the first time representatives of all araneoid families, including the first molecular data of the family Synaphridae. We use the resulting phylogenetic framework to study web evolution in araneoids. Araneoidea is monophyletic and sister to Nicodamoidea rank. n. Orbiculariae are not monophyletic and also include the RTA clade, Oecobiidae and Hersiliidae. Deinopoidea is paraphyletic with respect to a lineage that includes the RTA clade, Hersiliidae and Oecobiidae. The cribellate orb‐weaving family Uloboridae is monophyletic and is sister group to a lineage that includes the RTA Clade, Hersiliidae and Oecobiidae. The monophyly of most Araneoidea families is well supported, with a few exceptions. Anapidae includes holarchaeids but the family remains diphyletic even if Holarchaea is considered an anapid. The orb‐web is ancient, having evolved by the early Jurassic; a single origin of the orb with multiple “losses” is implied by our analyses. By the late Jurassic, the orb‐web had already been transformed into different architectures, but the ancestors of the RTA clade probably built orb‐webs. We also find further support for a single origin of the cribellum and multiple independent losses. The following taxonomic and nomenclatural changes are proposed: the cribellate and ecribellate nicodamids are grouped in the superfamily Nicodamoidea rank n. (Megadictynidae rank res. and Nicodamidae stat. n. ). Araneoidea includes 17 families with the following changes: Araneidae is re‐circumscribed to include nephilines , Nephilinae rank res., Arkyidae rank n. , Physoglenidae rank n. , Synotaxidae is limited to the genus Synotaxus, Pararchaeidae is a junior synonym of Malkaridae ( syn. n. ), Holarchaeidae of Anapidae ( syn. n. ) and Sinopimoidae of Linyphiidae ( syn. n. ).     

A phylogenetic study on genera of Cidariini from the Holarctic and the Indo-Australian areas (Lepidoptera: Geometridae: Larentiinae)

A cladistic analysis of forty-one species, belonging to ten genera, of the Cidariini sensu Herbulot from the Holarctic and the Indo-Australian areas, was performed using seventy-seven characters including larval and pupal data. Eight most parsimonious cladograms were found (length 398, CI 0.30, RI 0.70). The monophyly of the Cidariini is demonstrated, using selected species of Xanthorhoini sensu Herbulot as the outgroup. The relationships among the genera are as follows: ( Ecliptopera ( Eulithis ( Cidaria (( Plemyria ( Chloroclysta , Dysstroma ))(( Thera , Pennithera ) ( Heterothera ))))). This result suggests some taxonomic changes: Dysstroma Hübner, stat. rev. and Chloroclysta Hübner stat. rev. are sister taxa; Heterothera Inoue stat. rev. includes Viidaleppia Inoue, syn.n., Heterothera firmata (Hübner) comb.n. is transferred from Pennithera Viidalepp to Heterothera sensu lato . The results of confirmation and incongruence tests suggest that the characters from adult and immature stages exhibit the same evolutionary pattern. Thus the phylogeny derived from the combined data matrix does not give a misleading conclusion, even though there are many missing states in the larval data set.     

Revision of Microlaimidae, Erection of Molgolaimidae fam.n., and Remarks on the Systematic Position of Paramicrolaimus (Nematoda, Desmodorida)

The family Microlaimidae contains Bolbolaiminae subfam.n. (Bolbolaimus syn. Pseudomicro-laimus) and Microlaiminae ( Calomicrolaimus, Ixonema and Microlaimus ). The new family Molgolaimidae contains Aponematinae subfam.n. ( Aponema gen.n.) and Molgolaiminae subfam.n. ( Molgolaimus and Prodesmodora ). The main differentiating characters applied are: structures of the head region, shape of the oesophagus, position of the excretory pore, shape of the tail, structure of the gonads and ornamentation of the cuticle. The significance of porids and preanal supplements as distinguishing characters is, discussed. Microlaimidae are closely related to Desmodoridae; Molgolaimidae related to Spiriniidae. Paramicrolaimus is transferred from Microlaimidae to Spiriniidae.–Six species from the Øresund, Denmark, are redescribed: Microlaimus punctulatus Gerlach, 1950 and M. acinaces Warwick & Piatt, 1973; Aponema torosus (Lorenzen, 1973) gen.n., comb.n. (syn. Microlaimus torosus Loren-zen, 1973); Molgolaimus allgeni (Gerlach, 1950) comb.n. (syn. Microlaimus allgeni Gerlach, 1950) and M. turgofrons (Lorenzen, 1972) comb.n. (syn. Microlaimus turgofrons Lorenzen, 1972); Paramicrolaimus spirulifer Wieser, 1959.     

Jumping plant lice (Homoptera: Psylloidea) of the temperate neotropical region. Part 1: Psyllidae (subfamilies Aphalarinae, Rhinocolinae and Aphalaroidinae)

The psyllid-fauna of temperate and subantarctic South America comprises members of three families: Calophyidae, Triozidae and Psyllidae. Three subfamilies of the Psyllidae are revised in this paper: the Aphalarinae are represented by two species in two genera, one of which develops on Aquifoliaceae; the Rhinocolinae are represented by two congeneric species on Anacardiaceae while the Aphalaroidinae contain 38 species in seven genera trophically linked to the Compositae, Euphorbiaceae, Leguminosae, Myzodendraceae, Rhamnaceae, Solanaceae and Zygophyllaceae. The family Psyllidae (= Aphalaridae syn. nov. , =Spondyliaspididae syn. nov. ) and the constituent subfamily Aphalaroidinae (= Arepuninae syn nov. , = Ciriacreminae auct. pp) are redefined. Three genera and 30 species are described as new and two new generic, two new specific synonyms, and five new combinations are proposed. Information on larvae and host plant relationships is also given. Lectotypes are designated for eight species and a type-species is fixed for one genus. Keys are provided for the identification to species.     

Studies of some fungus gnats (Diptera: Mycetophilidae) including nine additions to the British list

Abstract A key is provided to the eight species of Anatella recorded in Britain, including three species newly recorded ( A.dampfi Landrock; A.gibba Winnertz; A.lenis Dziedzicki). A further six species are newly recorded from Britain ( Exechia sororcula Lackschewitz; Exechiopsis dumitrescae (Burghele-Balacesco); Allodia ( Brachycampta ) angulata Lundström; Mycetophila autumnalis Lundström; M.lubomirskii Dziedzicki; M.lunata Meigen); these and several other species are redescribed. The following nomenclatural changes are proposed. Exechia bicincta (Staeger) (= spinosa Bukowski, syn.n.); Mycetophila confusa Dziedzicki (= affluctata Edwards, syn.n.); Mycetophila dziedzickii nom.n. (= obscura Dziedzicki nec Walker). Female characters of seventeen of the twenty-two British species of Exechia and eight species of Mycetophila are discussed and illustrations provided.     

Phylogeny and classification of Cucujoidea and the recognition of a new superfamily Coccinelloidea (Coleoptera: Cucujiformia)

A large‐scale phylogenetic study is presented for Cucujoidea (Coleoptera), a diverse superfamily of beetles that historically has been taxonomically difficult. This study is the most comprehensive analysis of cucujoid taxa to date, with DNA sequence data sampled from eight genes (four nuclear, four mitochondrial) for 384 coleopteran taxa, including exemplars of 35 (of 37) families and 289 genera of Cucujoidea. Maximum‐likelihood analyses of these data present many significant relationships, some proposed previously and some novel. Tenebrionoidea and Lymexyloidea are recovered together and Cleroidea forms the sister group to this clade. Chrysomeloidea and Curculionoidea are recovered as sister taxa and this clade (Phytophaga) forms the sister group to the core Cucujoidea (Cucujoidea s.n .). The nitidulid series is recovered as the earliest‐diverging core cucujoid lineage, although the earliest divergences among core Cucujoidea are only weakly supported. The cerylonid series (CS) is recovered as monophyletic and is supported as a major Cucujiform clade, sister group to the remaining superfamilies of Cucujiformia. Currently recognized taxa that were not recovered as monophyletic include Cucujoidea, Endomychidae, Cerylonidae and Bothrideridae. Biphyllidae and Byturidae were recovered in Cleroidea. The remaining Cucujoidea were recovered in two disparate major clades: one comprising the nitidulid series + erotylid series + Boganiidae and Hobartiidae + cucujid series, and the other comprising the cerylonid series. Propalticidae are recovered within Laemophloeidae. The cerylonid series includes two major clades, the bothriderid group and the coccinellid group. Akalyptoischiidae are recovered as a separate clade from Latridiidae. Eupsilobiinae are recovered as the sister taxon to Coccinellidae. In light of these findings, many formal changes to cucujiform beetle classification are proposed. Biphyllidae and Byturidae are transferred to Cleroidea. The cerylonid series is formally recognized as a new superfamily, Coccinelloidea stat.n. Current subfamilies elevated (or re‐elevated) to family status include: Murmidiidae stat.n. , Teredidae stat.n. , Euxestidae stat.n. , Anamorphidae stat.rev. , Eupsilobiidae stat.n. , and Mycetaeidae stat.n. The following taxa are redefined and characterized: Cleroidea s.n. , Cucujoidea s.n. , Cerylonidae s.n. , Bothrideridae s.n. , Endomychidae s.n. A new subfamily, Cyclotominae stat.n. , is described. Stenotarsinae syn.n. is formally subsumed within a new concept of Endomychinae s.n.     

Revision of Scotocyma Turner (Lepidoptera: Geometridae: Larentiinae)

Abstract  The Australasian genus Scotocyma Turner is revised, containing the species S. albinotata (Walker), S. legalis (Warren), S. asiatica Holloway, S. scotopepla Prout, stat. n., S. manusensis Prout, stat. n., S. mimula (Warren), stat. n. and S. miscix Prout. Scotocyma euryochra Turner, syn. n., S. idioschema Turner, syn. n., S. ischnophrica Turner, syn. n. and S. transfixa Turner, syn. n. are regarded as synonyms of S. albinotata . Four species are described as new: S. samoensis , sp. n., S. sumatrensis , sp. n., S. rutilimixta , sp. n. and S. longiuncus , sp. n. Lectotypes are designated for S. scotopepla , S. manusensis and S. miscix . All species are illustrated, and keys to species and distribution maps are provided. A phylogenetic analysis was performed to test the monophyly of the genus and to examine distribution patterns of the species. A biogeographical discussion is included. The tribal position of the genus is clarified and relationships to closely related genera are discussed.     

A key to species of subgenus Lithochlaenius (Coleoptera, Carabidae, Chlaeniini, Chlaenius), with descriptions of three new species

Three new species of genus Chlaenius Bonelli subgenus Lithochlaenius Kryzhanovskij are described from China: Chlaenius chuanqianensis Liu & Liang, sp. n. (type locality: Xishui, Guizhou Province), Chlaenius linwensini Liu & Liang, sp. n. (type locality: Fujian Province), and Chlaenius propeagilis Liu & Kavanaugh, sp. n. (type locality: Gaoligongshan, Yunnan Province). Seven species of the subgenus are redescribed: Chlaenius agiloides Jedli?ka, Chlaenius formosensis Lorenz, Chlaenius agilis Chaudoir, Chlaenius leishanensis Kirschenhofer, Chlaenius noguchii Bates, Chlaenius rambouseki Lutshnik, and Chlaenius wrasei Kirschenhofer. Additional taxonomic changes include the following: Chlaenius formosanus Jedli?ka is treated as a junior synonym of Chlaenius rambouseki Lutshnik and Chlaenius anchomenoides Bates, syn. n. and Chlaenius nuristanus Jedli?ka as junior synonyms of Chlaenius agilis Chaudoir, syn. n.Chlaenius latroLaFerté-Sénectère is considered a nomen nudum stat. n. and unavailable, leaving Chlaenius agilisChaudoir as the next available name. Chlaenius nuristanusaberration rubridipesJedli?ka is also an unavailable name. Chlaenius formosensisLorenz (=Chlaenius formosanusHabu) is returned to species status stat. n. A key to adults of the 10 known species of subgenus Lithochlaenius is provided.     

A revision of the Oriental stonefly genus Phanoperla (Plecoptera: Perlidae)

The genus Phanoperla (=Dyaperla Banks, 1939) (Plecoptera: Perlidae: Perlini) is revised and generic diagnoses are provided for adults and larvae. Diagnostic and constitutive characters of the tribe Neoperlini are discussed, and Chinoperla Zwick, 1980, is shown to be the closest relative of Phanoperla. Many past misidentifications of Phanoperla species have been corrected by the use of characters recently recognized as important, namely the structure of the internal genitalia of male and female specimens and particularly the complex pattern of spines on the male penial sac made visible by eversion of this structure, and details of sculpturing of the egg chorion.
The following species of Phanoperla are recognized: amorpha sp.n.; anomala (Banks, 1939); bakeri (Banks, 1924); ceylonica Kawai, 1975; comuta sp.n.; flaveola (Klapálek, 1921), comb.n. ( =clarissa (Banks, 1913), syn.n.), (=Neoperla hageni Banks, 1920, syn.n.), (= N.consimilis Banks, 1924, syn.n.); guttata sp.n.; himalayana Zwick, 1977 (= siwalika Harper, 1977); limosa (Hagen, 1858); maculata sp.n.; maindroni (Navas, 1926), comb.n.; malayana sp.n.; minutissima (Enderlein, 1909); nana sp.n.; nervosa Banks, 1939; nuwara Kawai, 1975; omega sp.n.; pallipennis (Banks, 1938); parva sp.n.; pumilio (Klapálek, 1921), comb.n.; peniculus Kawai, 1969a; schmidi sp.n.; sertispina Jewett, 1975; srilanka sp.n.; sumatrae sp.n.; testacea (Hagen, 1858); wedda sp.n. P.claggi (Banks, 1938) is a nomen nudum.
All species are (re-)described and figured; all primary types have been examined. A key to species is provided. Most species can be assigned to one of seven species groups which are defined.
Phanoperla is endemic to the Oriental Region. Species groups are generally widespread, but individual species are in most cases known only from restricted areas.