Zootaxa

Abstract"Open ended" or "dark taxa" are species-rich clades that are so abundant and diverse that conventional taxonomic methods tend to struggle with the onslaught of specimens and species. New approaches based on presorting specimens to putative species with low-cost DNA barcodes may make tackling these taxa manageable. However, this will still require limiting the geographic scope of taxonomic revisions, given that most countries and biogeographic regions will have too many specimens and species for comprehensive coverage. We demonstrate the power of this approach by carrying out a revision of the Mycetophilidae fungus gnats (Diptera) of Singapore. The material revised here was obtained from 496 samples collected with 71 Malaise traps placed at 107 sites in different habitats in Singapore: mangroves, swamp forests, freshwater swamps, primary rainforests, and different types of secondary forests (old, maturing, young, urban). Based on molecular and morphological data for 1,454 specimens, we delimit 120 species of 23 genera. Of these, only five were species previously described. The remaining 115 species are new to science and described here. We name, however, only 98 of these species since 14 species are currently only known from females and we cannot prepare a fully satisfying morphological diagnosis (Manota spp. A-G and Neoempheria spp. A-G), and three species lack molecular data (Epicypta sp. A, Epicypta sp. B, and Neoempheria sp. H). To assess congruence between species delimited with DNA barcodes (3% clusters) and morphology, we determined a match ratio and found it to be overall high (95%) with even higher match ratios (99%) observed for MOTUs clustered at 5% with Objective Clustering and MOTUs obtained with ABGD set to (P=0.060). Overall, the ratio of undescribed to described is an astonishing 20:1. Only revising the Singapore fauna increases the number of described species of Oriental Mycetophilidae by about 25%, highlighting the size of the taxonomic impediment for fungus gnats. Most of the Singapore Mycetophilidae diversity belongs to three genera--Neoempheria Osten-Sacken (31 species), Epicypta Winnertz (29 species) and Manota Williston (14 species), but we also describe a new genus-- Integricypta, gen. n., which is the putative sistergroup of Aspidionia Colless--belonging to the Mycetophilinae Mycetophilini based on three species. The species sequenced, illustrated, and named are: Leptomorphus rafflesi, sp. n.; Monoclona simhapura, sp. n.; Azana demeijeri, sp. n.; Azana leekongchiani, sp. n. (Sciophilinae); Tetragoneura crawfurdi, sp. n.; Tetragoneura chola, sp. n.; Tetragoneura dayuan, sp. n.; Tetragoneura farquhari, sp. n.; Ectrepesthoneura johor, sp. n. (Tetragoneurinae); Mohelia zubirsaidi, sp. n.; Allactoneura tumasik, sp. n.; Allactoneura limbosengi, sp. n.; Manota banzu, sp. n.; Manota tantocksengi, sp. n.; Manota bukittimah, sp. n.; Manota chiamassie, sp. n.; Manota danmaxi, sp. n.; Manota mahuan, sp. n.; Manota temenggong, sp. n.; Clastobasis sritribuana, sp. n.; Clastobasis bugis, sp. n.; Clastobasis oranglaut, sp. n. (Leiinae); Parempheriella mait, sp. n.; Parempheriella longyamen, sp. n.; Parempheriella peranakan, sp. n.; Mycomya sachmatich, sp. n.; Neoempheria merlio, sp. n.; Neoempheria sabana, sp. n.; Neoempheria sangabo, sp. n.; Neoempheria shicheng, sp. n.; Neoempheria ujong, sp. n.; Neoempheria subaraji, sp. n.; Neoempheria kokoiyeeae, sp. n.; Neoempheria mandai, sp. n.; Neoempheria malacca, sp. n.; Neoempheria sinkapho, sp. n.; Neoempheria singapura, sp. n.; Neoempheria xinjiapo, sp. n.; Neoempheria puluochung, sp. n.; Neoempheria merdeka, sp. n.; Neoempheria neesoon, sp. n.; Neoempheria pulau, sp. n.; Neoempheria cinkappur, sp. n.; Neoempheria temasek, sp. n.; Neoempheria polunini, sp. n.; Neoempheria fajar, sp. n.; Neoempheria riatanae, sp. n. (Mycomyinae); Brachycampta glorialimae, sp. n.; Brachycampta murphyi, sp. n.; Brachycampta limtzepengi, sp. n.; Rymosia teopohlengi, sp. n.; Exechia tanswiehiani, sp. n.; Exechia alinewongae, sp. n.; Mycetophila chngseoktinae, sp. n.; Mycetophila georgettechenae, sp. n.; Mycetophila aishae, sp. n.; Platyprosthiogyne phanwaithongae, sp. n.; Platyprosthiogyne gohsookhimae, sp. n.; Platyprosthiogyne rahimahae, sp. n.; Platyprosthiogyne lynetteseahae, sp. n.; Platyprosthiogyne neilaae, sp. n.; Platyprosthiogyne snehalethaae, sp. n.; Platurocypta adeleneweeae, sp. n.; Platurocypta tanhoweliangi, sp. n.; Epicypta constancesingamae, sp. n.; Epicypta jennylauae, sp. n.; Epicypta limchiumeiae, sp. n.; Epicypta janetyeeae, sp. n.; Epicypta kohkhenglianae, sp. n.; Epicypta daintoni, sp. n.; Epicypta holltumi, sp.n.; Epicypta ridleyi, sp. n.; Epicypta chezaharaae, sp. n.; Epicypta tanjiakkimi, sp. n.; Epicypta gehminae, sp. n.; Epicypta jackieyingae, sp. n.; Epicypta khatijunae, sp. n.; Epicypta purchoni, sp. n.; Epicypta foomaoshengi, sp. n.; Epicypta ganengsengi, sp. n.; Epicypta nanyangu, sp. n.; Epicypta nus, sp. n.; Epicypta peterngi, sp. n.; Epicypta maggielimae, sp. n.; Epicypta yupeigaoae, sp. n.; Epicypta annwee, sp. n.; Epicypta wallacei, sp. n.; Epicypta lamtoongjini, sp. n.; Epicypta catherinelimae, sp. n.; Epicypta grootaerti, sp. n.; Epicypta joaquimae, sp. n.; Aspidionia cheesweeleeae, sp. n.; Aspidionia janetjesudasonae, sp. n.; Aspidionia fatimahae, sp. n.; Integricypta fergusondavie, sp. n.; Integricypta teosoonkimae, sp. n.; Integricypta shirinae, sp. n.; Integricypta hoyuenhoeae, sp. n. (Mycetophilinae). The previously described species are Metanepsia malaysiana Kallweit, Eumanota racola Soli, Parempheriella defectiva (Edwards), Neoempheria dizonalis (Edwards) (all known from Sumatra and/or the Malaysian peninsula), and Chalastonepsia hokkaidensis Kallweit a species spread in east Asia. The mycomyine genus Vecella Wu & Yang is here proposed as a new synonym to Parempheriella, with P. guadunana (Wu & Yang), n. comb. corresponding to an additional Palearctic species of Parempheriella. Barcodes for a second set of 1,493 Singapore mycetophilid specimens suggest the presence of an additional 18 MOTUs. We thus estimate that approximately 85% of all the Singapore species that routinely enter Malaise traps are identified or described here. The revision concludes with a discussion of the biogeography and generic composition of the mycetophilid fauna at the southern end of the Malay Peninsula. Zusammenfassung"Open-ended" oder "Dark Taxa" sind artenreiche Klade, die so abundant und arteinreich sind, dass die herkommlichen taxonomischen Methoden angesichts der gro{beta}en Anzahl von Exemplaren und Arten nicht gut funktionieren. Neue Ansatze, die auf das Vorsortierung von Exemplaren mit DNA Barcodes bis zum Artniveau basieren, erlauben es jetzt aber solche Taxa zu revidieren. Allerdings kann auch mit DNA Barcodes, nur die Fauna eines vergleichsweise kleinen Gebietes bearbeiten werden, weil fur die meisten Lander und biogeografischen Regionen zu viele Exemplare und Arten abgedeckt werden mussten. Wir demonstrieren hier wie eine solche Revision durchgefuhrt werden kann. Wir revidieren hier die Pilzmucken (Diptera: Mycetophilidae) von Singapur, die mit Malaisefallen gefangen werden konnen. Das hier uberarbeitete Material stammt aus 496 Malaise-Fallenproben, die mit 71 Malaise-Fallen an 107 Sammelstellen in verschiedenen Habitaten gefangen wurden: Mangroven, Sumpfwalder, Su{beta}wassersumpfe, Primarregenwalder und Sekundarwalder. Basierend auf molekularen und morphologischen Daten fur mehr als 1454 Tiere grenzen wir 120 Arten mit molekularen und morphologischen Daten ab, wobei nur 5 dieser Arten bereits beschrieben sind. Die verbleibenden 115 werden hier beschrieben. Allerdings benennen wir nur 98 Arten, da fur zwei Arten molekulare Daten fehlen und fur 14 weitere Arten derzeit nur Weibchen bekannt sind. Daher konnen wir derzeit keine zufriedenstellende morphologische Diagnose erstellen. Daruber hinaus fehlen molekulare Daten fur drei Arten (Epicypta sp. A, Epicypta sp. B und Neoempheria sp. H). Was die Artgrenzen betrifft, so stimmen die molekularen und morphologischen Daten in den meisten Fallen uberein (match ratio: 95% fur 3% MOTUs). Eine noch hohere "match ratio" von 99% wird fur 5% und ABGD MOTUs (P=0,060) beobachtet. Insgesamt ist das Verhaltnis zwischen unbeschrieben und beschrieben erstaunlich hoch (20:1), und die Uberarbeitung der singapurer Fauna erhoht die Anzahl der beschriebenen Arten in der Orientalischen Region um uber 25%. Dies unterstreicht den Ausma{beta} des "taxonomic impediments" fur Pilzmucken. Die meisten der Mycetophilidenarten in Singapur gehoren zu drei von 22 Gattungen - Neoempheria Osten-Sacken (31 Arten), Epicypta Winnertz (29 Arten) und Manota Williston (14 Arten), aber wir beschreiben hier auch eine neue Gattung, Integricypta, gen. n. basierend auf drei Arten. Die Gattung gehort zu den Mycetophilinae Mycetophilini und ist die mutma{beta}liche Schwestergruppe von Aspidionia Colless. Die sequenzierten, illustrierten und benannten Arten sind: Leptomorphus rafflesi, sp. n.; Monoclona simhapura, sp. n.; Azana demeijeri, sp. n.; Azana leekongchiani, sp. n. (Sciophilinae); Tetragoneura crawfurdi, sp. n.; Tetragoneura chola, sp. n.; Tetragoneura dayuan, sp. n.; Tetragoneura farquhari, sp. n.; Ectrepesthoneura johor, sp. n. (Tetragoneurinae); Mohelia zubirsaidi, sp. n.; Allactoneura tumasik, sp. n.; Allactoneura limbosengi, sp. n.; Manota banzu, sp. n.; Manota tantocksengi, sp. n.; Manota bukittimah, sp. n.; Manota chiamassie, sp. n.; Manota danmaxi, sp. n.; Manota mahuan, sp. n.; Manota temenggong, sp. n.; Clastobasis sritribuana, sp. n.; Clastobasis bugis, sp. n.; Clastobasis oranglaut, sp. n. (Leiinae); Parempheriella mait, sp. n.; Parempheriella longyamen, sp. n.; Parempheriella peranakan, sp. n.; Mycomya sachmatich, sp. n.; Neoempheria merlio, sp. n.; Neoempheria sabana, sp. n.; Neoempheria sangabo, sp. n.; Neoempheria shicheng, sp. n.; Neoempheria ujong, sp. n.; Neoempheria subaraji, sp. n.; Neoempheria kokoiyeeae, sp. n.; Neoempheria mandai, sp. n.; Neoempheria malacca, sp. n.; Neoempheria sinkapho, sp. n.; Neoempheria singapura, sp. n.; Neoempheria xinjiapo, sp. n.; Neoempheria puluochung, sp. n.; Neoempheria merdeka, sp. n.; Neoempheria neesoon, sp. n.; Neoempheria pulau, sp. n.; Neoempheria cinkappur, sp. n.; Neoempheria temasek, sp. n.; Neoempheria polunini, sp. n.; Neoempheria fajar, sp. n.; Neoempheria riatanae, sp. n. (Mycomyinae); Brachycampta glorialimae, sp. n.; Brachycampta murphyi, sp. n.; Brachycampta limtzepengi, sp. n.; Rymosia teopohlengi, sp. n.; Exechia tanswiehiani, sp. n.; Exechia alinewongae, sp. n.; Mycetophila chngseoktinae, sp. n.; Mycetophila georgettechenae, sp. n.; Mycetophila aishae, sp. n.; Platyprosthiogyne phanwaithongae, sp. n.; Platyprosthiogyne gohsookhimae, sp. n.; Platyprosthiogyne rahimahae, sp. n.; Platyprosthiogyne lynetteseahae, sp. n.; Platyprosthiogyne neilaae, sp. n.; Platyprosthiogyne snehalethaae, sp. n.; Platurocypta adeleneweeae, sp. n.; Platurocypta tanhoweliangi, sp. n.; Epicypta constancesingamae, sp. n.; Epicypta jennylauae, sp. n.; Epicypta limchiumeiae, sp. n.; Epicypta janetyeeae, sp. n.; Epicypta kohkhenglianae, sp. n.; Epicypta daintoni, sp. n.; Epicypta holltumi, sp.n.; Epicypta ridleyi, sp. n.; Epicypta chezaharaae, sp. n.; Epicypta tanjiakkimi, sp. n.; Epicypta gehminae, sp. n.; Epicypta jackieyingae, sp. n.; Epicypta khatijunae, sp. n.; Epicypta purchoni, sp. n.; Epicypta foomaoshengi, sp. n.; Epicypta ganengsengi, sp. n.; Epicypta nanyangu, sp. n.; Epicypta nus, sp. n.; Epicypta peterngi, sp. n.; Epicypta maggielimae, sp. n.; Epicypta yupeigaoae, sp. n.; Epicypta annwee, sp. n.; Epicypta wallacei, sp. n.; Epicypta lamtoongjini, sp. n.; Epicypta catherinelimae, sp. n.; Epicypta grootaerti, sp. n.; Epicypta joaquimae, sp. n.; Aspidionia cheesweeleeae, sp. n.; Aspidionia janetjesudasonae, sp. n.; Aspidionia fatimahae, sp. n.; Integricypta fergusondavie, sp. n.; Integricypta teosoonkimae, sp. n.; Integricypta shirinae, sp. n.; Integricypta hoyuenhoeae, sp. n. (Mycetophilinae). Die Tiere, die zu den bereits beschriebenen Arten gehoren, gehoren zu den folgenden Arten: Metanepsia malaysiana Kallweit, Eumanota racola Soli, Parempheriella defectiva (Edwards), Neoempheria dizonalis (Edwards) (alle Arten sind derzeit aus Sumatra und/oder der malaysischen Halbinsel bekannt), und Chalastonepsia hokkaidensis Kallweit, eine in Ostasien verbreitete Art. Die Gattung Vecella Wu & Yang wird hier als neues Synonym fur Parempheriella vorgeschlagen, wobei P. guadunana (Wu & Yang), n. comb., wobei die Gattung damit eine zusatzlichen palaarktischen Art erhalt. Die DNA Barcodes fur eine zweite Stichprobe mit 1.493 Pilzmucken deuten darauf hin, dass in Singapur 18 zusatzliche Arten mit Malaisefallen gefangen werden konnen. Es sieht aber dennoch so aus, als wurden wir bereits hier circa 85% aller Arten beschreiben, die regelma{beta}ig in Malaise-Fallen geraten. Die Revision endet mit einer Diskussion der Biogeographie und taxonomische Zusammensetzung der Mycetophilidenfauna im sudlichen Teil der Malaiischen Halbinsel.

Ninety hybotid species are recognized in the Botanic Garden Jean Massart (Brussels), representing 52 % of the hybotids ever recorded in Belgium. Two species new to science are described: Platypalpus massarti sp. nov. and P. pictitarsoides sp. nov. Following species are reported for the first time in Belgium: Drapetis infitialis (Collin, 1961), Platypalpus negrobovi Grootaert, Kustov & Shamshev, 2012 and Trichina opaca Loew, 1864. In addition, comments are given on a selected number of species: Bicellaria intermedia Lundbeck, 1910, Platypalpus aurantiacus (Collin, 1926), Platypalpus longimanus (Corti, 1907), Platypalpus nanus (Oldenberg, 1924), Platypalpus rapidoides Chvala, 1975, Platypalpus subtilis (Collin, 1926), Stilpon subnubilus Chvala, 1988 and on the genus Hybos Meigen, 1803. The holotype of P. cryptospina (Frey, 1909) is revised. Only 30 species or 33% of the species present are in a Safe/Low risk Red Data Book category meaning that the other 66% are in a more or less Threatened category.

The genus Farlowella has been historically challenging, in part due to the difficulty in defining diagnostic characters which allow to clearly set apart and identify the species. Farlowella colombiensis Retzer & Page 1997 is one of such examples, whose diagnostic characters were based on caudal-fin colour pattern, body cover ventral pattern, and details of the head. We herein reassess the taxonomic status of this species against congeners of the F. acus species group (F. acus, F. martini, F. mitoupibo, F. venezuelensis, and F. vittata). We found no significant differences between F. colombiensis and F. acus in morphometric, meristic, and discrete characters, therefore rendering Farlowella colombiensis a junior synonym of Farlowella acus. We provide remarks on different species of the F. acus group in Colombia, as well as description of sexual dimorphism in the genital papilla for the first time in the subfamily. We also provide a key to the species of the F. acus species group in Colombia.

This dataset provides photographic and morphological documentation of Stenopus spinosus Risso, 1827, based on a single adult specimen collected from Granadilla, Tenerife, Canary Islands, on 6 August 2025. The individual was observed and captured at a depth of 6 meters in a rocky overhead marine environment during a night dive, and subsequently documented through standardized dorsal-view laboratory imaging (Figures C-1 and D-1). Morphometric data were recorded, including carapace length (CL), rostrum length (RL), chela length and cheliped length. This record contributes to the regional documentation of marine decapods in the eastern Atlantic and supports ongoing biodiversity assessment efforts in the Canary Islands. Additionally, a separate in situ underwater observation of S. spinosus, recorded during a night dive in Jaca, Tenerife on 1 November 2024, is cited for comparative purposes. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=142 SRC="FIGDIR/small/669097v1_figC_1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@d301aeorg.highwire.dtl.DTLVardef@1138166org.highwire.dtl.DTLVardef@1948eaaorg.highwire.dtl.DTLVardef@225a7b_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure C-1.C_FLOATNO Dorsal view of Stenopus spinosus Risso, 1827 (Decapoda: Stenopodidea: Stenopodidae), adult specimen (Specimen ID: IMS-SSP-001) collected from Granadilla, Tenerife, Canary Islands (28{degrees}05'07''N, 16{degrees}29'23''W). The individual was encountered at a depth of 6 meters in a rocky overhead marine environment during a night dive at approximately 01:00 local time on 6 August 2025. Photographed under standardized laboratory conditions. Morphometric measurements: carapace length (CL) = 16.4 mm; rostrum length (RL) = 11.1 mm; right chela length = 36.7 mm; right cheliped length = 94.3 mm. Scale bar = 10 mm. Associated iNaturalist record: https://www.inaturalist.org/observations/304303255 C_FIG O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=142 SRC="FIGDIR/small/669097v1_figD_1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@1627499org.highwire.dtl.DTLVardef@d4eea5org.highwire.dtl.DTLVardef@17fca75org.highwire.dtl.DTLVardef@c4cf46_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure D-1C_FLOATNO Complete dorsal view of Stenopus spinosus Risso, 1827 (Decapoda: Stenopodidea: Stenopodidae), adult specimen (Specimen ID: IMS-SSP-001) showing extended antennal appendages. Collected at a depth of 6 meters within a rocky overhead marine environment during a night dive (approx. 01:00 local time) on 6 August 2025. Locality: Granadilla, Tenerife, Canary Islands (28{degrees}05'07''N, 16{degrees}29'23''W). Photographed under standardized laboratory conditions. Morphometric measurements: carapace length (CL) = 16.4 mm; rostrum length (RL) = 11.1 mm; right chela length = 36.7 mm. Scale bar = 10 mm. C_FIG

A new species of Protosticta Selys, 1885 (Odonata: Zygoptera: Platystictidae) is described based on two male specimens collected from Kerala, at the southern end of the Western Ghats in India. We compared P. armageddonensis sp. nov. with the three closely similar Protosticta species recently described from the Western Ghats, namely P.anamalaica Sadasivan, Nair & Samuel, 2022, P. cyanofemora Joshi, Subramanian, Babu & Kunte, 2020, and P. monticola Emiliyamma & Palot, 2016, to provide comprehensive differential diagnosis. The new species is distinguished from its congeners by a combination of characters, including the structure of prothorax, caudal appendages, genital ligula, and markings on the 8th abdominal segment. A revised key of Protosticta spp. of the Western Ghats, based on mature male specimens is provided.

Oceanic islands present very interesting environments, known by possessing relatively distinct fauna and flora. However, taxonomic accounts from Brazilian oceanic islands focused on important groups, such as the family Syllidae, began to be published only in recent years. In this paper we provide descriptions and illustrations of two new species, Brevicirrosyllis sp. nov. from Trindade Islands and Westheidesyllis sp. nov. from Rocas Atoll, two incertae sedis genera previously included in the Eusyllinae subfamily. We also provide updated identification keys for both genera.

In this paper we describe Testechiniscus sp. nov., a new tardigrade species from Novaya Zemlya, Russia, using data from morphological and morphometric analyses conducted with the use of light and scanning electron microscopy, as well as from genetic analysis based on four molecular markers (three nuclear: 18S rRNA, 28S rRNA, ITS-1, and one mitochondrial: COI). A comprehensive differential diagnosis is provided. Upon examination of both new and the type species we describe internal leg plates as a new character for the genus Testechiniscus, amending the genus diagnosis. This study introduces new data on the geographic distribution of Testechiniscus.

BackgroundA numer of Haliclona species (Demospongiae, Haplosclerida) in the Austin and McDaniel collections at the Royal British Columbia Museum (RBCM) are identified only to genus or genus and species. The collections are representative of over 40 years of sampling principally by the late Dr. William C. Austin and one of us (Neil McDaniel) through SCUBA diving on the west coast of British Columbia and specimens provided by others to Dr. Austin. We have selected representative Haliclona species in the collections for detailed examination and placement in subgenera and species (where species were not identified). Haliclona is recognized to have several subgenera, thus identification of specimens to genus and species is incomplete. Our study updates this status for the species examined. MethodsMethods of collection included intertidal scrapings or removal of non-encrusting specimens usually accompanied by in-situ photos, similar methods at SCUBA diving depths (subtidal to 35 m) and from other dredging, trawling and biological sampling activities. ResultsWe describe eleven new Haliclona (Demospongeae Haplosclerida Chalinadae) species and a range extension for Haliclona (Flagellia) edaphus de Laubenfels, 1930 for shallow waters of Southwestern British Columbia, Canada. New species include Haliclona (Gellius) hartmani n. sp., Haliclona (Gellius) shishalhensis n. sp., Haliclona (Reniera) gesteta n. sp., Haliclona (Rhizoniera) aborescens n. sp., Haliclona (Rhizoniera) blanca n. sp., Haliclona (Rhizoniera) boothensis n. sp., Haliclona (Rhizoniera) filix n. sp., Haliclona (Rhizoniera) kunechina n.sp., Haliclona (Rhizoniera) meandrina n. sp., Haliclona (Rhizoniera) penelakuta n. sp., and Haliclona (Rhizoniera) vulcana n. sp. We also redescribe Haliclona mollis (Lambe, 1893 [1894]) and propose placing it in the subgenus Haliclona. Except for Lambes syntype slides of Haliclona mollis which are deposited at the Canadian Museum of Nature, Ottawa, Canada, all holotypes and voucher specimens of species described are deposited at RBCM.

Ischyropsalis is a genus of harvestmen inhabiting both terrestrial and caves in central and southern Europe. The accepted number of species is controversial due to feature similarities and their strong sexual dimorphism. The northern part of the Iberian Peninsula harbours 11 accepted taxa, four of which are terrestrial, while the other seven exclusively live in caves. Some of these species have not been included in the only phylogenetic study conducted on this genus, so their taxonomic status has not been evaluated yet. In this context, we aim to unravel the phylogenetic relationships among the taxa within this genus, from the northern part of the Iberian Peninsula, by conducting morphological and phylogenetic analyses based on mitochondrial (COI) and nuclear (EF1-) molecular markers. Phylogenetic analyses revealed three previously undescribed species from karst caves in Cantabria and Asturias, herein described as I. damiani sp. nov., I. impressa sp. nov. and I. aguerana sp. nov.

Sponges of the Lower Greensand Group (LGS) are well preserved, and occur in sediments of a sandy matrix. Abundant in the Faringdon Sponge Gravel Member (FSG), these sponges, mostly Calcareans are found in Oxfordshire, with notable preservation at Little Coxwell quarries. Classical researchers described sponges and spicules from the LGS, including Lhuyd (considered to have been the first to publish illustrations of LGS sponges), Sharpe, Sowerby and Parkinson. In addition to the FSG, the Folkestone, Hythe, and Atherfield Clay formations within the LGS also contain sponge remains, including spicules as well as whole sponge fossils. These sponges include mostly samples from traditional sponge class Calcarea and a taxon of Hexactinellida; Altogether, the sponge assemblage developed in warm seas of the Lower Cretaceous, and display diverse shapes of sponge bodies and robust spicules. This study provides descriptions of common species following updated Porifera classification and recent sponge taxonomy research, illustrated with specimens from the Natural History Museum, London (NHM) and British Geological Survey (BGS) collections. The following taxa are recorded and described: 1) Calcareans: Barroisia anastomosans (Parkinson, 1811), Barroisia clavata (Keeping, 1883), Barroisia irregularis (Hinde, 1884), Dehukia crassa (de Fromentel, 1861), [Elasmoierea] faringdonensis (Mantell, 1854), [Elasmoierea] mantelli (Hinde, 1884), Peronidella gillieroni (Loriol, 1869), Peronidella prolifera (Hinde, 1884), Peronidella ramose (Roemer, 1839), Oculospongia dilatate (Roemer, 1864), Tremospongia pulvinaria (Goldfuss, 1826), Raphidonema contortum (Hinde, 1884), Raphidonema porcatum (Sharpe, 1854), Raphidonema farringdonensis (Sharpe, 1854), Raphidonema macropora (Sharpe, 1854), Raphidonema pustulatum Hinde, 1884, Endostoma foraminosa (Goldfuss, 1829); 2) Hexactinellids: Lonsda contortuplicata Lonsdale, 1849.

The paper presents new data on species composition and distribution of the genus Sympetrum in the extreme SW part of Romania. Two species, Sympetrum fonscolombii (Selys, 1840) and Sympetrum striolatum (Charpentier, 1840) are added to those of the literature - Sympetrum sanguineum (Muller, 1764) and Sympetrum meridionale (Selys, 1841) (Cirdei & Bulimar 1965). The sampled area was enlarged with new collecting sites. A brief description of species is given, especially the distinctive characters, including the hamular processes and the vulvar scale. The bifid aspect of the vulvar scale in S. meridionale indicates that the genus Sympetrum has a problem at least of species diagnosability.

During an expedition in June 2012 in Shache county of Tarim Basin in southern Xinjiang, China, a new species of the genus Dryomys (Gliridae) has been discovered and named Dryomys yarkandensis sp. nov. It has been found obviously different from D. nitedulai in northern Xinjiang, D. laniger, D. niethammeri and D. nitedulai in Europe, which are also belong to genus Dryomys. The new species Dryomys yarkandensis sp. nov is described below. HolotypeNo. N07, an adult female collected by Chen Zhenhai in June 2012, is deposited Center for disease prevention and control of Xinjiang (Xinjiang CDC). It was obtained from oasis orchard of desert in Tarim Basin (38{degrees}29N, 77{degrees}32E), 1211-1215 m. Genus characterThere is a dark chestnut round eye. The terminal of tail is club shape, covered with dense hairs, and cannot see the scale ring in external texture. Description of the speciesThe eyes is large. The beard is long and the longest could reach 30 mm. The tail is thicker and slightly longer than body length about 10%. The terminal of the tail is fluffy. All the surface is covered with dense hairs. External figureThe color of the new species on the back is lighter than that of D. laniger, D. niethammeri and D. nitedulai in Dryomys. The length of the tail is about 110% of the body length. The length of the ears is 12.8 mm, which is 15% shorter than the other three species of Dryomys. Skull and toothThe ratio between the length of audirory bullae and the breadth of auditory bullae is 1.66 (8.35/5.02), which is larger than the other three species of D. nitedula. The habitats of the new species is harsh, drought and hot in summer but dry and cold in winter. The habitats of D. nitedula in mountain valley in northern Xinjiang is temperate, humidity and low temperature, and there are berries or orchard.

The morphology and the anatomy of the copulatory apparatus in a Dugesiidae population from the SW Romania are presented. The copulatory apparatus is characterized by intermingled bursal canal musculature and two distinct penis bulbs with two large seminal vesicles. Based on these morphological characters, the population is assigned to the "lugubris-polychroa" group of species, now belonging to the genus Schmidtea (de Vries & Sluys 1991). The copulatory apparatus is also characterised by the presence of an atrial fold, characteristic of S. mediterranea. The assign of the morphotype here presented to the species level is delayed until integrative molecular analysis.

We present new distributional records of Argiope spiders in India, based on more than 10,000 digital images of the genus from the region curated by iNaturalist (www.inaturalist.org). Notable range expansions to India are documented for three species: A. chloreides Chrysanthus, 1961, A. mangal Koh, 1991, and A. sector (Forssk[a]l, 1776). Second, previously unrecorded field characters, updated distributional data, and a re-examination of published descriptions of type material, support the resurrection of A. undulata Thorell, 1887 as a valid species, long treated as a synonym of A. pulchella Thorell, 1881. Finally, we report the first in situ photographic records of live specimens of the rarely documented A. caesarea Thorell, 1897 and A. macrochoera Thorell, 1891. These varied findings for a small and conspicuous taxon highlight the value of online community-science platforms for documenting the arachnofauna of a biodiverse region, as well as illustrate the need for continued taxonomic review, even within well-known genera.

A new species of the genus Microhyla, Microhyla bengalensis sp. nov., described from West Bengal state, India. The new species is distinguished from its congeners by a combination of the following morphological characters: 1) Small in size (SVL= 16.2 mm. in male); 2) truncated snout in dorsal view; 3) head wider than long (HW: HL= 1.36); 4) canthus rostralis and tympanum are indistinct; 5) nostril placed on the dorsal side of the snout; 6) tibiotarsal articulation not reaching the eye; 7) fingers and toes without disc; 8) toe webbing basal; 9) thigh and foot length are equal and smaller than shank; 10) skin tuberculated on dorsum; 11) teddy bear dark brown mark on dorsum; 12) an inverted V-shaped dark brown mark above the vent. A comparative morphological data of all the 14 Indian species of Microhyla is also provided.

A new genus and species of the family Paradoxosomatidae from southern part of West Bengal, India is described. The new genus Manikidesmus gen. n. is diagnosed by combination of following characters: reduced paranota, distinct pleural keel, unpaired sternal lamella on 5th sternite, prefemur with setal brush, setal brush on tibia and tarsus in male, lamina medialis long straight with a curved hook, expanded post femoral lamina with a spine and tibiotarsus with a spine on the distofemoral process. The genus is distinguished from its Indian congeners by one or more diagnosed characters. In Manikidesmus suriensis, sp. n. tibia and tarsus bear setal brush in male (vs. absent in Oxidus and Chondromorpha), gonopod femur short, flat and without post femoral demarcation (vs. long, thin cylindrical with post femoral demarcation in Polydrepanum and Orthomorpha), tibiotarsus of gonopod long and a spine on the distofemoral process (vs. short and without spine in Anoplodesmus). In Kronopolites, coxa of gonopod densely bristled, collum with two rows of long bristles, femur long, slender and with a spine. All these characters are absent in the present genus. In Streptogonopus, gonopod femorite is distinctly demarcated from post femorite region and solenomere is twisted with solenophore but in the present species, femorite is not be separated from post femorite region and solenomere is free from solenophore.

Travassosinema bengalensis n. sp. is described from the hind gut of the spirobolid millipede, Trigoniulus corallinus (Gervais) from West Bengal, India. Females of the new species differ from the only known Indian species, T. travassosi Rao, 1958 by several characters namely tail length, length of oesophagous, size of egg, extension of umbraculum etc. It is very similar to other three species of Travassosinema, T. travassosi, T. thyropygi Hunt, 1996 and T. claudiae Morffe & Hasegawa, 2017 as all of them lack lateral alae and body contraction posterior to vulva. Except T. claudiae, it differs from all other species from millipedes by longest tail length (60% SL) and differs from T. claudiae by shorter oesophagous length and location of vulva. A new method for presentation of morphometric data (in percentage to standard length) in nematode is suggested. On the basis of phylogenetic analysis, it is suggested that umbraculum bearing genera, Indiana, Pulchrocephala should be excluded from the family Travassosinematidae.

The Mygalomorph spiders of the family Atypidae are among the most archaic spiders. The genus Atypus Latreille, 1804 occurs in Eurasia and northern Africa, with a single enigmatic species, Atypus snetsingeri Sarno, 1973, restricted to a small area in southeastern Pennsylvania in Eastern USA. This study was undertaken to learn more about genetics of that species, its habitat requirements and natural history. A close relationship to European species could be assumed based on A. snetsingeris occurrence on the eastern coast of the USA, however molecular markers (CO1 sequences) confirmed that A. snetsingeri is identical with Atypus karschi Donitz, 1887 native to East Asia; it is an introduced species. The specific epithet snetsingeri is therefore relegated to a junior synonym of A. karschi. The karyotype of A. karschi has 42 chromosomes in females and 41 in males (X0 sex chromosome system). Chromosomes were metacentric except for one pair, which exhibited submetacentric morphology. In Pennsylvania the above-ground webs are usually vertical and attached to the base of bushes, trees, or walls, although some webs are oriented horizontally near the ground. It was found in a variety of habitats from forests to suburban shrubbery, and over a wide range of soil humidity and physical parameters. Prey include millipedes, snails, woodlice, carabid beetles and earthworms. The number of juveniles in excavated female webs ranged from 70 to 201. Atypus karschi is the first known case of an introduced purse-web spider. It is rarely noticed but well-established within its range in southeastern Pennsylvania.

A new species of miniature sisorid catfish is described, from the upper Brahmaputra river drainage in northeastern India. The new species is distinguished from all its congeners except P. ferruginea and P. focusa by having an elongate light brown to cream marks either side on ventro-lateral margin just above anus. Further, distinguished from its congeners by the following combination of characters: presence of a W-shaped dark brown band on caudal fin, thoracic adhesive apparatus extending closer to pelvic-fin base, smooth anterior margin of dorsal spine, a narrow V-shaped light brown to cream bands on side of the body, dorsal-spine length (10.7-14.7% SL), dorsal-fin base length (10.7-14.2% SL), pectoral-fin spine length (14.0-21.1% SL), pelvic-fin length (13.5-16.6% SL), caudal peduncle length (14.4-18.2% SL) and depth (7.8-9.9% SL), total vertebrae (30-31), caudal fin with a complete medial hyaline bands towards its anterior end, reaching outer margin of each lobe. Other combination of characters differentiating the new species from its congeners are provided in the respective diagnoses.

In this paper it is described a new Sympetrum species - Sympetrum bigeminus sp. nov. from Romania. The male of this new species is similar almost to identity with Sympetrum sanguineum from which differs only in the more conspicuous lateral thoracic sutures. The females are different from Sympetrum sanguineum by the vulvar scale, which is prominent (well visible in lateral view), incurved, with a deep concavity, and shortly bilobed, thus showing morphological characters of a different and distinct species.