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A synopsis of Caribbean filistatid diversity is recorded herein. A new genus, Antilloides, is proposed for five new species exclusively found in the Antilles: A. abeli n. sp., A. cubitas n. sp., and A. mesoliticus n. sp. from Cuba; A. haitises n. sp. from the Dominican Republic; and A. zozo n. sp. from the U. S. Virgin Islands and Puerto Rico. The genus Filistatoides is revised and includes four species: the type species F. insignis F.O.P. Cambridge, which occurs only in Guatemala; the female is described here for the first time; F. polita Franganillo sp. reval., comb. nov., which occurs only in Cuba; F. xichu n. sp. described from Mexico; and F. milloti (Zapfe) which does not appear to belong to the genus based on morphological structures. Additionally, Kukulcania isolinae Alayón is synonymized with Kukulcania hibernalis (Hentz), and new records of its distribution are included for the Greater and Lesser Antilles.

The article contains a review of the type specimens of Sphecidae described by E. Eversmann, F. F. Morawitz, F. F. Kohl, V. V. Gussakovskij, V. L. Kazenas, A. S. Menke and Yu. Danilov, and deposited at the Zoological Institute of the Russian Academy of Sciences in St. Petersburg. Altogether 157 type specimens of 56 taxa were examined. Type specimens of Podalonia kozlovii (Kohl, 1906), whose depository was previously unknown, have been located.

Fifteen new species from six species groups of the genus Pholcus Walckenaer, 1805 are described from Southeast Asia: Pholcus hinsonensis sp. nov. (male & female, Thailand) and P. tharnlodensis sp. nov. (male & female, Thailand) from the P. bidentatus species group; P. kottawagamaensis sp. nov. (male & female, Sri Lanka) from the P. ethagala species group; P. cenranaensis sp. nov. (male & female, Indonesia) and P. krachensis sp. nov. (male, Thailand) from the P. gracillimus species group; P. anaiensis sp. nov. (male, Indonesia), P. ballarini sp. nov. (male & female, Thailand), P. gou sp. nov. (male & female, Myanmar), P. wan sp. nov. (male & female, Thailand) and P. zhuchuandiani sp. nov. (male & female, Indonesia) from the P. halabala species group; P. chiangmaiensis sp. nov. (male & female, Thailand) and P. taptaoensis sp. nov. (male & female, Thailand) from the P. quinquenotatus species group; P. kaebyaiensis sp. nov. (male & female, Thailand), P. musensis sp. nov. (male & female, Thailand) and P. songkhonensis sp. nov. (male & female, Thailand) from the P. yichengicus species group.

Three new species of oonopid spider from China are diagnosed, described and illustrated: Orchestina apiculata sp. nov. from Hunan, O. bialata sp. nov. and O. multipunctata sp. nov. from Jiangxi. The total number of the known species of Orchestina from China rises to 11 with the addition of three new species described in the present paper. Relationships with Asian and Afrotropical representatives are discussed.

The taxonomic knowledge on the desert-dwelling sparassid genus Cebrennus Simon, 1880 in Iran is updated by describing a new species, Cebrennus rambodjavani sp. nov. (male) from northern Qom in Iran's Central Desert, and reviewing the material of the previous Iranian record of the genus [sub C. kochi (O. Pickard-Cambridge, 1872)] from Bushehr, southern Iran, which is found to be a misidentification. A revised definition of the term "embolus kink", a male copulatory structure in Cebrennus, is given. A comparative discussion of this structure between several representatives of the genus Cebrennus is included.

Specimens were collected using pitfall traps. Coloration is described from alcohol-preserved specimens. Specimens were examined and measured using a Wild M5A stereomicroscope. Further details were studied and measured under an Olympus BX41 compound microscope. All drawings were made using a drawing apparatus attached to a Leica stereomicroscope. Male palps and female genitalia were examined and illustrated after they were dissected from the spiders' bodies. Photos were taken with an Olympus C7070 wide zoom digital camera mounted on an Olympus SZX12 stereomicroscope. The images were montaged using Helicon Focus image stacking software. Measurements of the legs are taken from the dorsal side. Total length of the body includes the chelicerae. All measurements were taken in mm. Abbreviations used in text include: AME, anterior median eyes; ALE, anterior lateral eyes; EM, embolus; MA, median apophysis; CD, copulatory duct; ST, spermatheca; fe, femur; pa, patella; ti, tibia; mt, metatarsus; p, prolateral; d, dorsal; r, retrolateral; v, ventral. Type specimens are deposited in the National Museum of Natural History (NMNHS), Sofia, Bulgaria.

A number of Australian species have been placed in the wrong, often non-Australian, genera. Some of these problems have been corrected here, by transfer or establishment of new genera. Several new species discovered during the course of the work are also described. Marptusa jovialis L. Koch, 1879 and Marptusa bracteata L. Koch, 1879 are transferred to Apricia gen. nov. Apricia longipalpis sp. nov. is also described from Australia. The study of the Australian species presently included in Trite Simon 1885 showed that this genus does not occur in mainland Australia. Hence, Marptusa vulpecula Thorell, 1881 is transferred to Capeyorkia gen. nov., while Marptusa longula Thorell, 1881 is transferred to Evarcha Simon, 1902. The only previously described 'Australian' species to remain in Trite is Trite concinna Rainbow, 1920, from Lord Howe Island and Norfolk Island in the Pacific, while Trite grayi sp. nov., also from Lord Howe Island, is described here. Trite concinna Rainbow 1920 is redescribed. Most specimens previous listed as this species from Lord Howe Island (including most of the syntype series) belong in Ancepitilobus howensis gen. nov. et sp. nov. Clynotis severus (L. Koch, 1879) is the solitary species that remains in Clynotis Simon, 1901, with the remainder of the mainland species being transferred to Pungalina Richardson, 2013: P. albobarbata (L. Koch, 1879) comb. nov., P. semiatra (L. Koch, 1879) comb. nov. and P. semiferruginea (L. Koch, 1879) comb. nov. Pungalina plurilineata sp. nov. and Pungalina waldockae sp. nov. are also described from Australia. Clynotis gratiosa from Lord Howe Island is formally transferred to Tara Peckham & Peckham, 1886, as suggested previously. Tara gratiosa (Rainbow, 1920) is redescribed. Finally, three names, Gangus longulus Simon, 1902, Trite ornata Rainbow, 1915 and Plexippus albopilosus Keyserling, 1883, are considered species inquirendae, due to the state or loss of type material.

Seven new species of the spider genus Xeropigo O. P.-Cambridge are described from Brazil, increasing the genus member list up to 16 species. X. piripiri n. sp., X. aitatu n. sp., and X. cajuina n. sp. are described from the state of Piauí. X. crispim n. sp. is described from the states of Ceará, Piauí, and Maranhão. X. oxente n. sp. is described from the state of Rio Grande do Norte. X. canga n. sp. is described from the state of Minas Gerais. X. ufo n. sp. is described from the state of Mato Grosso. The geographical distribution of X. tridentiger, X. camilae, X. pachitea, and X. perene is updated. A key to all species of Xeropigo is presented and possible relationships among all species of the genus are discussed.

The integration of independent data sets could solve problems in both traditional and DNA-based taxonomy. The aim of this study is to investigate the power of CO1 sequences and of morphometrics to distinguish closely related species in the spider genus Araniella. We put special emphasis on the species pair A. cucurbitina (Clerck, 1757) and A. opisthographa (Kulczyński, 1905) since the females are morphologically difficult to distinguish and often misidentified. A total of 216 sequences of eight Araniella species from seven European countries, North America and Asia were included in the molecular analysis. The results from both maximum likelihood and Bayesian phylogenetic inference indicate successful separation of six out of eight Araniella species, including A. cucurbitina and A. opisthographa. For the same six species, we detect no overlap of intra- and interspecific genetic divergence, leading to successful species identification with a threshold approach. In addition, morphometric analysis of the epigyna of A. cucurbitina and A. opisthographa supports species separation by two best explanatory ratios: receptaculum length and distance between receptaculum and copulatory duct. Although a small overlap in the ratios exists, the species identification rate increases when combining morphometric and molecular data, which demonstrates the efficiency of integrative approaches for distinguishing closely related species. However, none of the molecular approaches was able to separate closely related A. alpica (L. Koch, 1869) and A. inconspicua (Simon, 1874) due to shared CO1 haplotypes. Considering the clear morphological separation of the males and different habitat preferences, incomplete lineage sorting or introgressive hybridization could have led to identical CO1 sequences. Therefore, DNA-barcoding must be thoroughly tested even within small homogenous genera of spiders.

A new ricinuleid species, Cryptocellus chimaera sp. nov., is described based on a male specimen from Northwest Ecuador (Esmeraldas, Reserva Ecológica Mache-Chindul, Estación Biológica Bilsa). This species is unique among all Cryptocellus in having very large longitudinal carapacial translucent areas together with a markedly incrassate femur of leg II. Representing only the second species of the order described from Ecuador, C. chimaera sp. nov. is assigned to the magnus species-group of Cryptocellus Westwood, 1874. Cryptocellus chimaera sp. nov. is remarkable, for its morphology resembles that of Cryptocellus magnus Ewing, 1929, especially with regard to the male copulatory apparatus, although both resemble Pseudocellus Platnick, 1980, due to the presence of diffuse longitudinal carapacial translucent areas. Along with the new species description, a comparative diagnosis and supplementary images are provided for C. magnus. Based on direct observations of some species belonging to the five species-groups of Cryptocellus, we discuss on the occurrence of different morphologies of carapacial translucent areas within the genus. We deem it important to continue the survey of morphological characters, especially within Cryptocellus, in order to increase our understanding of the species-groups and to unravel their relationships.

Hoedillus sexpunctatus Simon, 1898 was described from a single female specimen collected in Guatemala and is the type species of the monotypic genus Hoedillus Simon, 1898. This genus was originally placed in the family Sparassidae Bertkau, 1872, subfamily Heteropodinae Thorell, 1873. In a review of this subfamily, Jäger (2002) determined that Hoedillus was misplaced in Sparassidae due to the lack of metatarsal trilobate membranes. Hoedillus was transferred to the family Zoridae Pickard-Cambridge, 1893 by Jäger (2002), now a junior synonym of Miturgidae Simon, 1886 (Ramírez 2014). Ramírez (2014), suggested Hoedillus may be a member of the Xenoctenus group, but provisionally listed it as a Miturgidae, awaiting further investigation.

The present paper describes nine new Otacilia species from Southwest China: O. mira sp. nov. (♀, ♂) and O. pyriformis sp. nov. (♀, ♂) from Chongqing, O. papilion sp. nov. (♀, ♂) from Guizhou, O. aurita sp. nov. (♀, ♂), O. digitata sp. nov. (♂), O. leibo sp. nov. (♀, ♂) and O. ovata sp. nov. (♀, ♂) from Sichuan, O. acuta sp. nov. (♀, ♂) and O. flexa sp. nov. (♀, ♂) from Yunnan. Line drawings, photos and descriptions of all new species are presented. In addition, the 21 known Chinese Otacilia species are divided into three species groups.

A faunistic survey on Chañaral Island, Atacama, near the northern Pacific coast of Chile, allowed the discovery and description of a new species of the spider genus Cyrioctea: C. islachanaral sp. nov., based on females collected by pitfall traps. Strikingly, this new species shares morphological characters with some Southern African representatives of this genus rather than with the species of continental South America. The male of the species C. cruz Platnick, previously known from continental Chile (northern Coquimbo), is described for the first time based on specimens collected in the same locality.

Spiders (Araneae) are unique regarding their respiratory system: they are the only animal group that breathe simultaneously with lungs and tracheae. Looking at the physiology of respiration the existence of tracheae plays an important role in spiders with a well-developed tracheal system. Other factors as sex, life time, type of prey capture and the high ability to gain energy anaerobically influence the resting and the active metabolic rate intensely. Most spiders have metabolic rates that are much lower than expected from body mass; but especially those with two pairs of lungs. Males normally have higher resting rates than females; spiders that are less evolved and possess a cribellum have lower metabolic rates than higher evolved species. Freely hunting spiders show a higher energy turnover than spiders hunting with a web. Spiders that live longer than 1 year will have lower metabolic rates than those species that die after 1 year in which development and reproduction must be completed. Lower temperatures and starvation, which most spiders can cope with, will decrease the metabolic rate as well.

Draposa Kronestedt, 2010 is a small genus of Pardosinae spiders. Currently it encompasses 10 species (World Spider Catalog 2016) distributed from Pakistan to Southeast China. Most species of the genus, except for D. porpaensis (Gajbe, 2004), are known from both sexes and were described or redescribed by Kronestedt (2010). Two other species, D. amkhasensis (Tikader & Malhotra, 1976) and D. burasantiensis (Tikader & Malhotra, 1976), both recently transferred to Draposa (Dhali et al. 2012 ), are doubtful because their copulatory organs are not properly illustrated and differ from the type species and other species of the genus. The male of Draposa subhadrae (Patel & Reddy, 1993) remains known by very poor original drawings because Kronestedt (2010) was not able to study types. While studying material from Sri Lanka collected by us, we found one sample with two females belonging to D. subhadrae and two males of Draposa having the same colour pattern and size. We concluded that these specimens are conspecific. The goal of this paper is to provide an illustrated redescription of this species.

The hitherto Afrotropical corinnid spider genus Cambalida Simon, 1909 is recorded from Asia for the first time. Detailed morphological descriptions and genitalic illustrations of two new species, C. deorsa sp. n. and C. tuma sp. n. from India, are provided. One new combination is proposed: Cambalida flavipes (Gravely, 1931) comb. nov. The occurrence of distal femoral constrictions of III and IV legs of both male and female are recognised as additional somatic features for the genus Cambalida. The current distribution of all the three Indian Cambalida spp. is mapped.

The family Anyphaenidae is composed by 56 genera and 542 species worldwide (World Spider Catalog 2015). These spiders, known as "ghost spiders", are wandering hunters living in a variety of environments, from forests to deserts, and can be quite abundant in different crops such as cotton, sorghum and rice (Brescovit 1996; Young & Edwards 1990; Taylor & Pfannenstiel 2008). They typically live on vegetation, among dead leaves or under loose bark and rocks (Richman & Ubick 2005) but synanthropic associations have been reported for a few species (Jiménez 1998; Guarisco 1999; Durán-Barrón et al. 2009). The genus Anyphaena has 81 species widely distributed in Asia, Central Europe, North America and Mexico (Brescovit 1996; Richman & Ubick 2005; World Spider Catalog 2015). The species from Noth America and Mexico were revised by Platnick (1974) who recognized four species groups (accentuata, celer, pectorosa and pacifica). Platnick (1977), Platnick & Lau (1975) and Brescovit & Lise (1989) complemented the revision of the genus in Central America. Presently, there are 27 species of Anyphaena recorded in Mexico (World Spider Catalog 2015), 24 of them from the celer group. Here, two new species of Anyphaena are described based in material collected during an inventory of spiders associated to houses in Mexico City, carried out by Durán-Barrón et al. (2009). Both species have the diagnostic characters of the members of the pacifica group as defined by Platnick (1974), such as the lack of leg coxal spurs and the presence of a lightly sclerotized atrium in the female epigynum. These species represent the first record of the pacifica group in Mexico. The occurrence of Anyphaenidae associated to houses was reported in Mexico by Durán-Barrón et al. (2009), who recorded Anyphaena obregon Platnick & Lau, 1975 and Hibana futilis (Banks, 1898) as frequent inhabitants inside houses. The species herein described are reported solely from urban areas and can be also characterized as frequent in these anthropic environments.

The genus Stenaelurillus Simon, 1886 is known from 35 species worldwide, including 27 species from Africa and eight from Asia (four species known from India, one from Iran, one from China, one from Tibet and one from Vietnam) (World Spider Catalog 2016). The four species known from India are S. albus Sebastian et al., 2015, S. jagannathae Das, Malik & Vidhel, 2015, S. lesserti Reimoser, 1934 and S. sarojinae Caleb & Mathai, 2014 (Prószyński 2015; World Spider Catalog 2016). The present paper contains description of Stenaelurillus metallicus sp. nov., discovered from scrub jungle remnants of tropical dry evergreen forests, a unique habitat found in Madras Christian College campus, Chennai, Tamil Nadu, India.

Currently the linyphiid genus Taranucnus includes four species: T. setosus (O. P.-Cambridge, 1863), the type species with Palearctic distribution, T. bihari Fage, 1931 (Eastern Europe), T. nishikii Yaginuma, 1972 (Japan) and T. ornithes (Barrows, 1940)(USA). In Ukraine Taranucnus is represented by two species, T. setosus and T. bihari. A detailed study of the male mentioned earlier as Taranucnus sp. (Chumak, Prokopenko & Tymochko 2007; Prokopenko, Chumak 2007), and several females close to T. bihari Fage, 1931 revealed a new species of this genus. Since it is hard to clarify the position of some of these females we report them below as T. cf. bihari.

The spiders of the genus Neoxyphinus Birabén differ from those of other oonopid genera by the male endites with an api-cal, retrolateral excavation bearing a subapical tooth-like apophysis and, in females, by the ellipsoid genital atrium, with angular lateral margins. In this paper, eleven new species of the genus are described, mainly from northern South America: N. amazonicus Moss & Feitosa, sp. nov. (♂♀) from Colombia and Brazil; N. macuna Moss & Ruiz, sp. nov. (♂♀), N. tuparro Moss & Ruiz, sp. nov. (♂) and N. pure Moss & Bonaldo, sp. nov. (♂♀) from Colombia; N. yekuana Moss & Feitosa, sp. nov. (♂♀), N. trujillo Moss & Bonaldo, sp. nov. (♂♀), N. yacambu Moss & Feitosa, sp. nov. (♂) and N. saarineni Moss & Bonaldo, sp. nov. (♂) from Venezuela; N. inca Moss & Ruiz, sp. nov. (♂♀) from Peru; N. beni Moss & Feitosa, sp. nov. (♂♀) from Bolivia; and N. coca Moss & Feitosa, sp. nov. (♂♀) from Ecuador.

Spiders are an important animal group, with a long history. Details of their origins remain limited, with little knowledge of their stem group, and no insights into the sequence of character acquisition during spider evolution. We describe a new fossil arachnid, Idmonarachne brasierigen. et sp. nov. from the Late Carboniferous (Stephanian,ca 305-299 Ma) of Montceau-les-Mines, France. It is three-dimensionally preserved within a siderite concretion, allowing both laboratory- and synchrotron-based phase-contrast computed tomography reconstruction. The latter is a first for siderite-hosted fossils and has allowed us to investigate fine anatomical details. Although distinctly spider-like in habitus, this remarkable fossil lacks a key diagnostic character of Araneae: spinnerets on the underside of the opisthosoma. It also lacks a flagelliform telson found in the recently recognized, spider-related, Devonian-Permian Uraraneida. Cladistic analysis resolves our new fossil as sister group to the spiders: the spider stem-group comprises the uraraneids and I. brasieri While we are unable to demonstrate the presence of spigots in this fossil, the recovered phylogeny suggests the earliest character to evolve on the spider stem-group is the secretion of silk. This would have been followed by the loss of a flagelliform telson, and then the ability to spin silk using spinnerets. This last innovation defines the true spiders, significantly post-dates the origins of silk, and may be a key to the group's success. The Montceau-les-Mines locality has previously yielded a mesothele spider (with spinnerets). Evidently, Late Palaeozoic spiders lived alongside Palaeozoic arachnid grades which approached the spider condition, but did not express the full suite of crown-group autapomorphies., (© 2016 The Authors.)

Here we report the larval phytophagous habit of Litoleptis for the first time, and describe six new species of Litoleptis in Japan; L. japonica n. sp., L. kiiensis n. sp., L. niyodoensis n. sp., L. himukaensis n. sp., L. izuensis n. sp., and L. asterellaphile n. sp. All the species described here are thallus-miners of liverworts belonging to Aytoniaceae and Conocephalaceae (Marchantiopsida: Marchantiophyta). Each fly species mined thalli of only one of the following genera: Conocephalum, Reboulia, and Asterella. The descriptions of the Japanese Litoleptis species here expand the concept of this genus. The female genital morphology of Litoleptis strengthened the current placement of Litoleptis as a member of Spaniinae.

The National Park of Dadia in NE Greece (Thrace) was established as a nature reserve in 1980, mainly due to its great diversity in birds of prey. Since then many studies have taken place, focusing on other birds, reptiles, amphibians and some invertebrates (grasshoppers, beetles and butterflies), but up to now none was conducted on spiders. The aim of the present paper was to create the first extensive checklist on the spiders of this important natural reserve. For this purpose, pitfall traps were set in 15 sites located in and around the National Park, resulting in a large spider collection. The results of the taxonomical revision of this collection are here presented, giving rise to 132 species in total, which belong to 24 families. Of them, 11 species (Centromerus valkanovi Deltshev, 1983, Crosbyarachne silvestris (Georgescu, 1973), Ipa terrenus (L. Koch, 1879), Sintula spiniger (Balogh, 1935), Tenuiphantes floriana (van Helsdingen, 1977), Alopecosa taeniopus (Kulczyñski, 1895), Liocranum rupicola (Walckenaer, 1830), Zodarion turcicum Wunderlich, 1980, Gnaphosa modestior Kulczyñski, 1897, Philodromus krausi Muster & Thaler, 2004, Cozyptila thaleri Marusik & Kovblyuk, 2005) are new records for the Greek territory. Seven species (Dysdera kati sp. n., Dysdera krisis sp. n., Harpactea ice sp. n., Harpactea wolfgangi sp. n.-Dysderidae, Phrurolithus thracia sp. n.-Phrurolithidae, Zodarion beroni sp. n.-Zodariidae, Drassyllus dadia sp. n.-Gnaphosidae) are here proposed as new species for science.

Flirtea C.L. Koch, 1839, is one of the oldest genera described in Cosmetidae, currently including 30 species mostly from the Andes. Its type species, Cosmetus pictus Perty, 1833, from Brazil, the type material of which is long lost, has since long been misidentified in the literature due to a redescription based on another unrelated species, while the true F. picta was widely known as Flirtea phalerata C.L. Koch, 1840. This unrelated species is here described as Cynorta pictoides sp. nov. Flirtea picta is here redescribed based on abundant material collected in the Brazilian Atlantic Forest biome from Bahia state, and a neotype is designated for its type species. Here, we propose a particular pattern of a white mask blot on the dorsal scutum be called "scaramuccia", and variation in this pattern is described. Genital morphology of Flirtea picta is described for the first time. Flirtea is rediagnosed and most species currently assigned to Flirtea are suggested to belong to other genera. Cynorta valida Roewer, 1928 and Paecilaema batman Pinto-da-Rocha & Yamaguti, 2013 are newly transferred to Flirtea, yielding the new combinations Flirtea valida and Flirtea batman.

The tanagers (Thraupidae) are a major component of the Neotropical avifauna, and vary in plumage colors, behaviors, morphologies, and ecologies. Globally, they represent nearly 4% of all avian species and are the largest family of songbirds. However, many currently used tanager genera are not monophyletic, based on analyses of molecular data that have accumulated over the past 25 years. Current genus-level classifications of tanagers have not been revised according to newly documented relationships of tanagers for various reasons: 1) the lack of a comprehensive phylogeny, 2) reluctance to lump existing genera into larger groups, and 3) the lack of available names for newly defined smaller groups. Here, we present two alternative classifications based on a newly published comprehensive phylogeny of tanagers. One of these classifications uses existing generic names, but defines them broadly. The other, which we advocate and follow here, provides new generic names for more narrowly defined groups. Under the latter, we propose eleven new genera (Asemospiza, Islerothraupis, Maschalethraupis, Chrysocorypha, Kleinothraupis, Castanozoster, Ephippiospingus, Chionodacryon, Pseudosaltator, Poecilostreptus, Stilpnia), and resurrect several generic names to form monophyletic taxa. Either of these classifications would allow taxonomic authorities to reconcile classification with current understanding of tanager phylogenetic relationships. Having a more phylogenetically accurate classification for tanagers will facilitate the study and conservation of this important Neotropical radiation of songbirds.

Four new species of Psechrus are described from Yunnan Province: P. changminae sp. nov., P. conicus sp. nov., P. discoideus sp. nov. and P. spatulatus sp. nov. Herewith the number of species belonging to Psechrus in Yunnan Province extended from five to nine. Illustrations and colour photos are provided, with comparison of intraspecific variation of copulatory organs.

The Oriental armored spider genus Shearella Lehtinen, 1981 is recorded for the first time from India. Detailed description and illustrations of both sexes of Shearella alii sp. nov. are given. The geographic distribution of the genus is updated. Sinamma sanya (Lin & Li, 2010) is transferred back to Shearella, and Shearella browni (Shear, 1978) back to Monoblemma Gertsch, 1941. A checklist of all Indian tetrablemmid species currently known and a distribution map of all known Shearella spp. are presented.

The genus Rualena Chamberlin & Ivie 1942 (Araneae: Agelenidae) is revised and a new genus, Hoffmannilena, is described. Four new species are described for Rualena: R. cedros sp. nov. (♂ ♀), R. parritas sp. nov. (♂ ♀), R. thomas sp. nov. (♂ ♀), and R. ubicki sp. nov. (♀). The males of R. alleni Chamberlin & Ivie 1942 and R. avila Chamberlin & Ivie 1942 and the female of R. rua (Chamberlin 1919) are described for the first time. Rualena goleta Chamberlin & Ivie 1942 is a junior synonym of R. surana Chamberlin & Ivie 1942. Rualena cavata (F.O. Pickard-Cambridge 1902) and R. pasquinii Brignoli 1974 are considered incertae sedis. Two species are transferred from Rualena to Novalena Chamberlin & Ivie 1942: N. shlomitae (García-Villafuerte 2009) comb. nov. and N. simplex (F.O. Pickard-Cambridge 1902) comb. nov. For Hoffmannilena gen. nov., five new species are described: H. apoala sp. nov. (♀), H. cumbre sp. nov. (♂ ♀), H. huajuapan sp. nov. (♀), H. mitla sp. nov. (♀), and H. tizayuca sp. nov. (♂ ♀). Three species are transferred from Novalena to Hoffmannilena gen. nov.: H. lobata (F.O. Pickard-Cambridge 1902) comb. nov., H. marginata (F.O. Pickard-Cambridge 1902) comb. nov., and H. variabilis (F.O. Pickard-Cambridge 1902) comb. nov. Novalena cuspidata (F.O. Pickard-Cambridge 1902) is a junior synonym of H. marginata.

Neostasina gen. nov. is proposed to include the type species, Neostasina macleayi (Bryant, 1940) comb. nov., and four other described species: N. lucasi (Bryant, 1940) comb. nov. and N. saetosa (Bryant, 1948) comb. nov., transferred from Stasina Simon, 1877, N. bicolor (Banks, 1914) comb. nov., from Olios Walckenaer, 1837, and N. antiguensis (Bryant, 1923) comb. nov., from Pseudosparianthis Simon, 1887. Stasina portoricensis Petrunkevitch, 1930 and Olios darlingtoni Bryant, 1942 are considered junior synonyms of N. bicolor comb. nov. All species are redescribed and illustrated. Twenty-two new species are described, namely: N. baoruco sp. nov. (♀), N. bermudezi sp. nov. (♂, ♀) and N. cachote sp. nov. (♀) from the Dominican Republic, N. bryantae sp. nov. (♂, ♀), N. granpiedra sp. nov. (♂, ♀), N. iberia sp. nov. (♂, ♀), N. montegordo sp. nov. (♀), N. siempreverde sp. nov. (♂) and N. turquino sp. nov. (♀) from Cuba, N. croix sp. nov. (♂) from the Island of St. Croix and N. virginensis sp. nov. (♀) from the Island of St. John, both U.S. Virgin Islands, N. guanaboa sp. nov. (♂), N. gunboat sp. nov. (♂), N. jamaicana sp. nov. (♀), N. liguanea sp. nov. (♂, ♀), N. lucea sp. nov. (♀), N. mammee sp. nov. (♂, ♀), and N. maroon sp. nov. (♂, ♀) from Jamaica, N. ouali sp. nov. (♂, ♀) from Nevis Island, N. amalie sp. nov. (♂, ♀) from U.S. (St. John and St. Thomas Islands) and British Virgin Islands (Peter Island and Sandy Cay), and N. taino sp. nov. (♂, ♀) from Puerto Rico and Dominican Republic. An identification key and distribution maps are provided for all known species.

Acantholycosa Dahl, 1908 is a relatively large genus, comprising 29 species to date (World Spider Catalog 2015). The genus is well delimited; its members are recognized by having 4-6 pairs of ventral spines at leg I, a wide embolus (sometimes with a spine at its base), apical pocket(s) of epigyne separated from fovea, among other characters (cf. Marusik et al. 2004, 2015). Acantholycosa is the among the better known genera of Holarctic Lycosidae due to several revisions and reviews (Kronestedt & Marusik 2002; Marusik et al. 2004, 2015; Marusik & Logunov 2011; Marusik & Omelko 2011). Most Acantholycosa are known from the Altai-Sayan mountain system (21 species, of which 17 are local endemics) and the Maritime Province of Russia (6 species, three are local endemics). Although the Russian Far East is well studied, an expedition to the previously unstudied Phalaza Mt. in the south part of Maritime Province revealed a new species closely related to A. azarkinae Marusik & Omelko, 2011. The main goal of this paper is to provide detailed description of this new species.

Six new taxa of Campodeidae (Diplura) are described in the genera Litocampa, Juxtlacampa, Oncinocampa, and Tachycampa. We also redescribe the interesting species Juxtlacampa juxtlahucensis Wygodzinsky, 1944 from Juxtlahuaca cave in Guerrero, Mexico. All of these taxa are cave-dwelling species with more or less noticeable troglobiomorphic features They inhabit the subterranean ecosystem in six limestone massifs and one lava tube cave in the central states of Mexico. Four of these species are included in the "tachycampoide" group and one species in the "podocampoide" group (sensu Bareth & Conde). Nine species already known in Central and South America of the "tachycampoide" group, in such poorly-sampled regions compared with the eight species in the well-sampled Mediterranean region (Ibero-Sardinia and north Africa), suggest an American origin for this group.

A new species, Pardosa koponeni sp. n., is described. The new species is widely distributed in Far East Asia. It was previously confused with P. lugubris (Walckenaer, 1802). The two species have very similar copulatory organs but differ in the colouration of legs II-IV in males and the carapace/femur I ratio in both sexes. The distribution of the new species is mapped using material examined and literature data. To provide a more complete understanding of the boundaries between such closely related species, morphological and DNA barcoding approaches for species discrimination were integrated. Two species of the Pardosa lugubris-group (P. lugubris and P. alacris) were found to share haplotypes, suggesting evidence of hybridization or incomplete lineage sorting, or they are perhaps separate morphotypes of the same species. This is another example of complexity and the value of comparing morphology and DNA barcode data among spiders.

A taxonomic revision and phylogenetic analysis of the spider genus Glenognatha Simon, 1887 is presented. This analysis is based on a data set including 24 Glenognatha species plus eight outgroups representing three related tetragnathine genera and one metaine as the root. These taxa were scored for 78 morphological characters. Parsimony was used as the optimality criterion and a sensitivity analysis was performed using different character weighting concavities. Seven unambiguous synapomorphies support the monophyly of Glenognatha. Some internal clades within the genus are well-supported and its relationships are discussed. Glenognatha as recovered includes 27 species, four of them only known from males. A species identification key and distribution maps are provided for all. New morphological data are also presented for thirteen previously described species. Glenognatha has a broad distribution occupying the Neartic, Afrotropic, Indo-Malaya, Oceania and Paleartic regions, but is more diverse in the Neotropics. The following eleven new species are described: G. vivianae n. sp., G. caaguara n. sp., G. boraceia n. sp. and G. timbira n. sp. from southeast Brazil, G. caparu n. sp., G. januari n. sp. and G. camisea n. sp. from the Amazonian region, G. mendezi n. sp., G. florezi n. sp. and G. patriceae n. sp. from northern Andes and G. gouldi n. sp. from Southern United States and central Mexico. Females of G. minuta Banks, 1898, G. gaujoni Simon, 1895 and G. gloriae (Petrunkevitch, 1930) and males of G. globosa (Petrunkevitch, 1925) and G. hirsutissima (Berland, 1935) are described for the first time. Three new combinations are proposed in congruence with the phylogenetic results: G. argyrostilba (O. P.-Cambridge, 1876) n. comb., G. dentata (Zhu & Wen, 1978) n. comb. and G. tangi (Zhu, Song & Zhang, 2003) n. comb., all previously included in Dyschiriognatha Simon, 1893. The following taxa are newly synonymized: Dyschiriognatha montana Simon, 1897, Glenognatha mira Bryant, 1945 and Glenognatha maelfaiti Baert, 1987 with Glenognatha argyrostilba (Pickard-Cambridge, 1876) and Glenognatha centralis Chamberlin, 1925 with Glenognatha minuta Banks, 1898.

The spider genus Chrysometa Simon, 1895 comprises 138 species of small (3-5 mm) Neotropical orb-weavers spiders (Nogueira et al. 2011; World Spider Catalogue 2015) mainly associated with arboreal vegetation from intermediate to low altitude forests (Levi 1986). Males of Chrysometa differ from other tetragnathids by having the palpal tibial length approximately as long as its widest point; paracymbium articulated and with several apophyses located at both ends; male cephalic region narrower than in the female and having cymbial ectobasal and ectomedian processes. Females are diagnosed by having femora without trichobothria; abdomen covered with silver guanine patches; a flat epigynum and also by their fertilization ducts originating anteriorly and crossing over the spermathecae (Levi 1986; Alvarez-Padilla & Hormiga 2011).

We revise the Neotropical spider genus Gelanor Thorell, 1869 (Mimetidae). Gelanor is distributed from northeast Mexico to southern Uruguay , from sea level to 1,600 m. We describe five new species of Gelanor and report eleven new synonymies. Gelanor is here circumscribed to include ten species: Gelanor fortuna new species, Gelanor juruti new species, Gelanor moyobamba new species, Gelanor siquirres new species, Gelanor waorani new species, Gelanor altithorax Keyserling, 1893 (= Gelanor lanei Soares, 1941 new synonymy), Gelanor consequus O. P.-Cambridge, 1902 (= Gelanor depressus Chickering, 1956 new synonymy, Gelanor gertschi Chickering, 1947 new synonymy and Gelanor heraldicus Petrunkevitch, 1925 new synonymy), Gelanor innominatus Chamberlin, 1916, Gelanor latus (Keyserling, 1881) (= Gelanor mixtus O. P.-Cambridge, 1899 new synonymy, Gelanor mabelae Chickering, 1947 new synonymy, Gelanor ornatus Schenkel, 1953 new synonymy and Gelanor proximus Mello-Leitão, 1929 new synonymy) and Gelanor zonatus (C.L. Koch, 1845) (= Gelanor distinctus O-P. Cambridge, 1899 new synonymy, Gelanor insularis Mello-Leitão, 1929 new synonymy and Gelanor obscurus Mello-Leitão, 1929 new synonymy). In addition, we describe for the first time the males of G. altithorax and G. consequus. Species descriptions are provided for all ten species in the genus, together with a compilation of available data, including type specimens, type localities and morphological diagnoses. Light and electron microscope images and updated data on known geographical distributions, are also provided. We also discuss the phylogenetic placement of Gelanor in Mimetidae.

Three new species of Kalcerrytus Galiano, 2000 from the state of Pará in the Brazilian Amazon are described: K. amplexus sp. nov. from Parque Nacional da Serra do Pardo, São Félix do Xingu, K. filipi sp. nov. from Reserva Ecológica do Jari, Almeirim, and K. leonardi sp. nov. from Juruti. These increase up to 18 the described species within the genus.

The tetragnathid genus Chrysometa Simon, 1894 includes 138 species found in the Americas, ranging from the Caribbean to Chile (World Spider Catalog 2015). This genus was revised by Levi (1986), with more recent publications adding to the genus (Álvarez-Padilla 2007, Nogueira et al. 2011, Simó et al., in press). Following Álvarez-Padilla & Hormiga (2011), Chrysometa is differentially diagnosed from other American tetragnathids based on the male palp with a cymbial ectobasal process, cymbial ectomedian process, and embolic basal process, and a paracymbium articulated with a membrane. The epigynum is flat, with fertilization ducts present. Both sexes have guanine crystals in their abdomen and femora lacking trichobothria. Three Jamaican Chrysometa are known: C. pecki Levi, 1986, C. fuscolimbata (Archer, 1958) and C. linguiformis (Franganillo, 1930); all of them known from females only (Levi 1986).

Two new species, Tropizodium kalami sp. n. and Tropizodium viridurbium sp. n. from the genus Tropizodium are described from India. Detailed morphological descriptions, diagnostic features and illustrations of copulatory organs are given. Distribution of both the new species is mapped.

Oligomely is an anomaly manifested in the morphology of spiders (except for deformations of the prosoma and exoskeleton), by the absence of one or more appendages, and in their anatomy by the absence of neuromeres. This study was aimed at determining whether there is a correlation between the absence of a neuromere or its half in the subesophageal ganglia and the volume of the prosoma. Morphometric studies involved oligomelic specimens of Tegenaria atrica with the absence of one walking leg and two walking legs. Volumetric analysis concerned with nymph stage II of spiders obtained after exposing the embryos to alternating temperatures of 14 and 320C. The results were compared with those obtained from the histological analysis of the prosoma and central nervous system of control individuals. It was found that there was no relationship between the absence of half or an entire neuromere and the volume of the prosoma of oligomelic specimens. The volume of the central nervous system decreased but the volume change was not proportional to the changes in the prosoma volume. During studies, it was found that the lack of neuromeres resulted in an increase in the volume of remaining neuromeres.

Three new Nemesia Audouin 1826 species from northern and central Italy are named. They share a combination of sexual characters, not found in other described species. A new species-complex within Nemesia is here referred to as the apenninica group. Within the apenninica group, N. apenninica n. sp., N. hastensis n. sp., and N. pedemontana n. sp. differ in the morphology of the male palpal organ and the female spermathecae. The three species have different kinds of geographical distributions. While N. apenninica and N. hastensis have locally restricted and geographically separated distributions, the distribution of N. pedemontana overlaps with that of both of these species and extends widely in northern and central Italy. In its periphery, the distribution of N. pedemontana overlaps with that of species other than the apenninica group, e.g., N. meridionalis (Costa, 1835) in southern Italy and N. manderstjernae (L. Koch, 1871) and N. carminans (Latreille, 1818) in Liguria. Information on burrow structure, phenology and habitat are provided for all three new species. Some aspects of the behavior and feeding are discussed for N. pedemontana and N. hastensis.

A new species belonging to the kinabaluensis group of the trachelid genus Utivarachna Kishida, 1940, U. lata sp. nov., is described from China. The male of U. fabaria Zhao & Peng, 2014 is described here for the first time based on specimens collected from Yunnan Province, China. The type material of U. gui (Zhu, Song & Kim, 1998) is re-examined and the species is redescribed.

The Afrotropical dark sac spider genus Messapus Simon, 1898 (Corinnidae: Corinninae) currently only comprises two described species, the type species M. martini Simon, 1898 and M. natalis (Pocock, 1898), which have both recently been redescribed. The leg and setal morphology of Messapus is studied using scanning electron microscopy for the first time, for M. martini and M. tigris sp. n., and additional characters are provided to supplement a recent generic description. Five new species are described in the current paper: M. megae sp. n. (♂ ♀, from Zimbabwe), M. meridionalis sp. n. (♀, from South Africa), M. seiugatus sp. n. (♀, from Guinea), M. tigris sp. n. (♀, from Botswana and Namibia), and M. tropicus sp. n. (♂ ♀, from Democratic Republic of the Congo). All five species are arboreal spiders occurring on bark, lower foliage strata and the canopies of forest and savannah trees. An identification key to the seven species of the genus is provided.

Three new species of the uloborid genus Orinomana Strand, O. penelope n. sp. from Ecuador, O. viracocha n. sp. from Peru, and O. florezi n. sp. from Colombia, are described. Additionally, the male of O. ascha Grismado, from Northwestern Argentina, is described for the first time. This material includes the first males known of the genus, providing diagnostic characters for its recognition; the complex and massive embolus with several branches is proposed as a synapomorphy of the genus.

Elaver O. Pickard-Cambridge, 1898 is characterized and redescribed, including 49 species occurring from the United States to Argentina. Thirty seven previously known species are redescribed: Elaver achuca (Roddy, 1966) revalidated, E. balboae (Chickering, 1937), E. barroana (Chickering, 1937), E. calcarata (Kraus, 1955), E. carlota (Bryant, 1940), E. chisosa (Roddy, 1966), E. crinophora (Franganillo, 1934), E. crocota (O. Pickard-Cambridge, 1896), E. albicans (Franganillo, 1930) name restored, E. depuncta O. Pickard-Cambridge, 1898, E. elaver (Bryant, 1940), E. excepta (L. Koch, 1866), E. grandivulva (Mello-Leitão, 1930), E. hortoni (Chickering, 1937), E. implicata (Gertsch, 1941), E. juana (Bryant, 1940), E. kohlsi (Gertsch & Jellison, 1939), E. linguata (F.O. Pickard-Cambridge, 1900), E. madera (Roddy, 1966), E. mirabilis (O. Pickard-Cambridge, 1896) new. comb., E. mulaiki (Gertsch, 1935), E. multinotata (Chickering, 1937), E. orvillei (Chickering, 1937), E. placida O. Pickard-Cambridge, 1898, E. portoricensis (Petrunkevitch, 1930), E. quadrata (Kraus, 1955), E. richardi (Gertsch, 1941), E. sericea O. Pickard-Cambridge, 1898, E. sigillata (Petrunkevitch, 1925), E. simplex (O. Pickard-Cambridge, 1896), E. texana (Gertsch, 1933), E. tigrina O. Pickard-Cambridge, 1898 name restored, E. tricuspis (F.O. Pickard-Cambridge, 1900), E. tristani (Banks, 1909), E. tumivulva (Banks, 1909), E. valvula (F.O. Pickard-Cambridge, 1900) and E. wheeleri (Roewer, 1933). Ten new species are described: E. candelaria n. sp. and E. helenae n. sp. from Mexico; E. arawakan n. sp. from Haiti; E. lizae n. sp. from Costa Rica; E. darwichi n. sp. from Ecuador; E. juruti n. sp., E. tourinhoae n. sp. and E. vieirae n. sp. from Brazil; E. shinguito n. sp. from Peru and E. beni n. sp. from Bolivia. The female of E. hortoni is described for the first time. Lectotypes are designated for E. sigillata and its actual female is described for the first time. Four new synonyms are proposed: E. languida (Gertsch, 1941) is synonimized with E. multinotata; E. dorothea (Gertsch, 1935) with E. wheeleri; E. exempta (Gertsch & Davis, 1940) with E. placida and E. vulnerata (Kraus, 1955) with E. calcarata. The drawings in the original descriptions of E. kawitpaaia (Barrion & Litsinger, 1995) and E. turongdaliriana (Barrion & Litsinger, 1995) are sufficiently informative to exclude these species from Elaver but not to accurately establish its generic affiliation. Thus, until the types become available for examination, these species must remain as Clubionidae incertae sedis. Heterochemmis (F.O. Pickard-Cambridge, 1900) is synonymized with Elaver and Heterochemmis mutatus Gertsch & Davis,1940 is recognized as a junior synonym of Elaver mirabilis n. comb., the type species of Heterochemmis. New records are presented for E. valvula, E. balboae, E. brevipes (Keyserling, 1891), E. grandivulva and E. lutescens (Schmidt, 1971). Two species described by Franganillo, E. tenera (Franganillo, 1935) and E. tenuis (Franganillo, 1935), are considered species inquirendae.

Urupuyu gen. nov. is described for three new species of small black jumping spiders from the cloud forests of Ecuador: Urupuyu antisana sp. nov. (type species), U. edwardsi sp. nov., and U. occidentale sp. nov. Phylogenetic analyses with DNA sequences (28S, actin 5C, wingless, 16SND1 and CO1) indicate Urupuyu is closely related to the huriine amycoids Hurius and Scoturius, a placement also supported by morphological traits. Our phylogenetic analysis serves to clarify the relationships within the Amycoida in general, leading to our proposing a revised classification for the group, with subfamilies Gophoinae, Sitticinae, Bredinae subfam. nov., Scopocirinae, Thiodininae, Sarindinae, Huriinae, Simonellinae, and Amycinae. We confirm the marpissine-like Breda belongs within the Amycoida. The phylogeny implies that ant mimicry has evolved at least twice (simonellines and sarindines) and probably a third time (Atomosphyrus in the thiodinines) within the Amycoida. The following new synonymies are proposed for suprageneric names: Hyetusseae Simon, 1903 and Arachnomureae Mello-Leitão, 1917 = Thiodininae Simon, 1901; Zunigeae Simon, 1901 = Sarindinae Simon, 1901; Synemosynae Banks, 1892 = Simonellinae Peckham, Peckham & Wheeler, 1888; Magoninae Petrunkevitch, 1928 = Amycinae F.O.P.-Cambridge, 1900.

Tarodes Pocock, 1899 and Udvardya Prószyński, 1992 are redefined and redescribed. The male of T. lineatus Pocock, 1899 and the female of U. elegans Prószyński, 1992 are redescribed for comparisons. Additionally, two species of Udvardya from New Guinea, U. bellatrix sp. nov. and U. fortis sp. nov., are diagnosed, described and illustrated. Geographical distribution of the species is given.

The Indo-pacific araneid genus Anepsion, with A. rhomboides (L. Koch, 1867) as the type species, was erected by Strand in 1929. He proposed the name Anepsion as a replacement name for Anepsia L. Koch, 1871, preoccupied by Anepsia Gistl, 1848, a dipteran genus (OBIS Australia, 2015). The genus was revised by Chrysanthus (1961, 1969) and currently has 16 described species and 1 subspecies (World Spider Catalog 2015). In the present paper, we are reporting the genus from India for the first time and synonymising Cyrtarachne keralensis Jose, 2011 with Anepsion maritatum O. Pickard-Cambridge, 1877. A redescription and illustrations of both male and female of A. maritatum are provided.

Freyinae, new subfamily, is described for a group of genera of Neotropical jumping spiders that can be distinguished from other non-ant mimic salticoid Neotropical salticids by having the following three morphological features: a slightly more elongate carapace, a distinctive prolateral tibial macrosetae arrangement (medially placed subdistal and subproximal macrosetae, with a subdorsal medial macroseta in some males), and an unusual dorsoventrally thick tegulum basal division (although one or two of these features are sometimes lost). It includes 20 genera previously considered valid, of which 19 are retained: Akela Peckham & Peckham, 1896, Aphirape C.L. Koch, 1850, Asaracus C.L. Koch, 1846, Capidava Simon, 1902, Chira Peckham & Peckham, 1896, Edilemma Ruiz & Brescovit, 2006, Eustiromastix Simon, 1902, Freya C.L. Koch, 1850, Frigga C.L. Koch, 1850, Kalcerrytus Galiano, 2000, Nycerella Galiano, 1982, Onofre Ruiz & Brescovit, 2007, Pachomius Peckham & Peckham, 1896, Phiale C.L. Koch, 1846, Rishaschia Makhan, 2006, Sumampattus Galiano, 1983, Trydarssus Galiano, 1995, Tullgrenella Mello‑Leitão, 1941, and Wedoquella Galiano, 1984. Romitia Caporiacco, 1947 (and its synonym Uspachus Galiano, 1995) is synonymized with Pachomius, new synonymy. New genera described in the subfamily are: Drizztius, Leptofreya, Megafreya, Philira, Tarkas, Triggella, and Xanthofreya. The following nomenclatorial changes are made: New synonyms: Freya demarcata Chamberlin & Ivie, 1936 = Freya (sub Cyrene) albosignata (F.O.P.-Cambridge, 1901); Freya (sub Cyrene) grisea (F.O.P.-Cambridge, 1901) = Freya (sub Cyrene) infuscata (F.O.P.-Cambridge, 1901); Freya (sub Cyrene) emarginata (F.O.P.-Cambridge, 1901) and Nycerella (sub Heraclea) sanguinea paradoxa (Peckham & Peckham, 1896) = Nycerella (sub Heraclea) sanguinea (Peckham & Peckham, 1896); Pachomius (sub Phiale) maculosus (Chickering, 1946) = Phiale (sub Cyrene) bilobata (F.O.P.-Cambridge, 1901); Phiale (sub Cyrene) mediocava (F.O.P.-Cambridge, 1901) = Freya (sub Cyrene) maculatipes (F.O.P.-Cambridge, 1901); Phiale (sub Cyrene) simplicicava (F.O.P.-Cambridge, 1901) = Freya (sub Cyrene) bifurcata (F.O.P.-Cambridge, 1901). New combinations: Capidava rufithorax Simon, 1902 = Drizztius rufithorax; Freya frontalis Banks, 1929 = Eustiromastix frontalis; Chira (sub Attus) spinipes (Taczanowski, 1872) = Eustiromastix spinipes; Freya (sub Euophrys) ambigua (C.L. Koch, 1846) = Leptofreya ambigua; Freya (sub Cyrene) bifurcata (F.O.P.-Cambridge, 1901) = Leptofreya bifurcata; Freya (sub Cyrene) laticava (F.O.P.-Cambridge, 1901) = Leptofreya laticava; Freya (sub Cyrene) longispina (F.O.P.-Cambridge, 1901) = Leptofreya longispina; Phiale (sub Cyrene) bilobata (F.O.P.-Cambridge, 1901) = Pachomius bilo-batus; Phiale (sub Cyrene) hieroglyphica (F.O.P.-Cambridge, 1901) = Pachomius hieroglyphicus; Phiale (sub Cyrene) niveoguttata (F.O.P.-Cambridge, 1901) = Pachomius niveoguttatus; Romitia (sub Euophrys) albipalpis (Taczanowski, 1878) = Pachomius albipalpis; Romitia (sub Euophrys) andina (Taczanowski, 1878) = Pachomius andinus; Romitia (sub Uspachus) bahiensis (Galiano, 1995) = Pachomius bahiensis; Romitia (sub Uspachus) columbiana (Galiano, 1995) = Pachomius columbianus; Romitia (sub Uspachus) juquiaensis (Galiano, 1995) = Pachomius juquiaensis; Romitia (sub Phiale) ministerialis (C.L. Koch, 1846) = Pachomius ministerialis; Romitia (sub Uspachus) misionensis (Galiano, 1995) = Pachomius misionensis; Romitia nigra Caporiacco, 1947 = Pachomius nigrus; Romitia (sub Uspachus) patellaris (Galiano, 1995) = Pachomius patellaris; Chira (sub Diagondas) micans (Simon, 1902) = Philira micans; Chira superba Caporiacco, 1947 = Philira superba; Freya (sub Cyrene) maculatipes (F.O.P.-Cambridge, 1901) = Tarkas maculatipes; Freya (sub Cyrene) bifida (F.O.P.-Cambridge, 1901) = Triggella bifida; Freya infuscata (F.O.P.-Cambridge, 1901) = Triggella infuscata; Freya (sub Cyrene) minuta (F.O.P.-Cambridge, 1901) = Triggella minuta; Freya (sub Cyrene) albosignata (F.O.P.-Cambridge, 1901) = Xanthofreya albosignata; Freya arraijanica Chickering, 1946 = Xanthofreya arraijanica; Phiale (sub Cyrene) bicuspidata (F.O.P.-Cambridge, 1901) = Xantho-freya bicuspidata; Freya chionopogon Simon, 1902 = Xanthofreya chionopogon; Freya (sub Heraclea) rustica (Peckham & Peckham, 1896) = Xanthofreya rustica. Combinations restored: Phiale (sub Pachomius) flavescens (Peckham & Peckham, 1896) = Pachomius flavescens; Phiale (sub Pachomius) similis (Peckham & Peckham, 1896) = Pachomius similis. Invalid name: Freya dyali Roewer 1951 is an invalid replacement name for Euophrys trifasciata "Dyal 1935", which was a redescription of Euophrys trifasciata C.L. Koch, 1846, not a homonym. New species: Drizztius geminensis. First female descriptions and transfers of mismatched females: First descriptions for Asaracus megacephalus C.L. Koch, 1846, Capidava biuncata Simon, 1902, and Phiale formosa (Banks, 1909); the true female of Eustiromastix spinipes is described, and its mismatched female is identified as the female of Eustiromastix falcatus Galiano, 1981; the mismatched female of Freya (sub Cyrene) prominens (F.O.P.-Cambridge, 1901) is identified as the female of Xanthofreya rustica; the misidentified female of X. rustica is identified as the female of Leptofreya bifurcata. Lectotypes: designated for Cyrene bifida F.O.P.-Cambridge, 1901 and Cyrene formosa Banks, 1909. New synapomorphy: a constricted proximal end of the cymbium of the male palp is an apparent new synapomorphy for Salticoida.

The superfamily Austrochiloidea (Austrochilidae and Gradungulidae) take a pivotal position in araneomorph spider phylogeny. In this discussion crevice weaver spiders (Filistatidae) are of equal interest. Especially data from these phylogenetically uncertain yet basal off branching groups can enlighten our understanding on the evolution of organ systems. In the course of a survey on the evolutionary morphology of the circulatory system in spiders we therefore investigated the hemolymph vascular system in two austrochiloid and one filistatid species. Additionally some data on a hypochilid and a gradungulid species are included. Using up-to-date morphological methods, the vascular systems in these spiders are visualized three dimensionally. Ground pattern features of the circulatory systems in austrochiloid spiders are presented and the data discussed along recent lines of phylogenetic hypotheses. Special topics highlighted are the intraspecific variability of the origins of some prosomal arteries and the evolutionary correlation of respiratory and circulatory systems in spiders., (Copyright © 2015 Elsevier Ltd. All rights reserved.)