The spider tree of life: phylogeny of Araneae based on target-gene analyses from an extensive taxon sampling.

We present a phylogenetic analysis of spiders using a dataset of 932 spider species, representing 115 families (only the family Synaphridae is unrepresented), 700 known genera, and additional representatives of 26 unidentified or undescribed genera. Eleven genera of the orders Amblypygi, Palpigradi, Schizomida and Uropygi are included as outgroups. The dataset includes six markers from the mitochondrial (12S, 16S, COI) and nuclear (histone H3, 18S, 28S) genomes, and was analysed by multiple methods, including constrained analyses using a highly supported backbone tree from transcriptomic data. We recover most of the higher-level structure of the spider tree with good support, including Mesothelae, Opisthothelae, Mygalomorphae and Araneomorphae. Several of our analyses recover Hypochilidae and Filistatidae as sister groups, as suggested by previous transcriptomic analyses. The Synspermiata are robustly supported, and the families Trogloraptoridae and Caponiidae are found as sister to the Dysderoidea. Our results support the Lost Tracheae clade, including Pholcidae, Tetrablemmidae, Diguetidae, Plectreuridae and the family Pacullidae (restored status) separate from Tetrablemmidae. The Scytodoidea include Ochyroceratidae along with Sicariidae, Scytodidae, Drymusidae and Periegopidae; our results are inconclusive about the separation of these last two families. We did not recover monophyletic Austrochiloidea and Leptonetidae, but our data suggest that both groups are more closely related to the Cylindrical Gland Spigot clade rather than to Synspermiata. Palpimanoidea is not recovered by our analyses, but also not strongly contradicted. We find support for Entelegynae and Oecobioidea (Oecobiidae plus Hersiliidae), and ambiguous placement of cribellate orb-weavers, compatible with their non-monophyly. Nicodamoidea (Nicodamidae plus Megadictynidae) and Araneoidea composition and relationships are consistent with recent analyses. We did not obtain resolution for the titanoecoids (Titanoecidae and Phyxelididae), but the Retrolateral Tibial Apophysis clade is well supported. Penestomidae, and probably Homalonychidae, are part of Zodarioidea, although the latter family was set apart by recent transcriptomic analyses. Our data support a large group that we call the marronoid clade (including the families Amaurobiidae, Desidae, Dictynidae, Hahniidae, Stiphidiidae, Agelenidae and Toxopidae). The circumscription of most marronoid families is redefined here. Amaurobiidae include the Amaurobiinae and provisionally Macrobuninae. We transfer Malenellinae (Malenella, from Anyphaenidae), Chummidae (Chumma) (new syn.) and Tasmarubriinae (Tasmarubrius, Tasmabrochus and Teeatta, from Amphinectidae) to Macrobuninae. Cybaeidae are redefined to include Calymmaria, Cryphoeca, Ethobuella and Willisius (transferred from Hahniidae), and Blabomma and Yorima (transferred from Dictynidae). Cycloctenidae are redefined to include Orepukia (transferred from Agelenidae) and Pakeha and Paravoca (transferred from Amaurobiidae). Desidae are redefined to include five subfamilies: Amphinectinae, with Amphinecta, Mamoea, Maniho, Paramamoea and Rangitata (transferred from Amphinectidae); Ischaleinae, with Bakala and Manjala (transferred from Amaurobiidae) and Ischalea (transferred from Stiphidiidae); Metaltellinae, with Austmusia, Buyina, Calacadia, Cunnawarra, Jalkaraburra, Keera, Magua, Metaltella, Penaoola and Quemusia; Porteriinae (new rank), with Baiami, Cambridgea, Corasoides and Nanocambridgea (transferred from Stiphidiidae); and Desinae, with Desis, and provisionally Poaka (transferred from Amaurobiidae) and Barahna (transferred from Stiphidiidae). Argyroneta is transferred from Cybaeidae to Dictynidae. Cicurina is transferred from Dictynidae to Hahniidae. The genera Neoramia (from Agelenidae) and Aorangia, Marplesia and Neolana (from Amphinectidae) are transferred to Stiphidiidae. The family Toxopidae (restored status) includes two subfamilies: Myroinae, with Gasparia, Gohia, Hulua, Neomyro, Myro, Ommatauxesis and Otagoa (transferred from Desidae); and Toxopinae, with Midgee and Jamara, formerly Midgeeinae, new syn. (transferred from Amaurobiidae) and Hapona, Laestrygones, Lamina, Toxops and Toxopsoides (transferred from Desidae). We obtain a monophyletic Oval Calamistrum clade and Dionycha; Sparassidae, however, are not dionychans, but probably the sister group of those two clades. The composition of the Oval Calamistrum clade is confirmed (including Zoropsidae, Udubidae, Ctenidae, Oxyopidae, Senoculidae, Pisauridae, Trechaleidae, Lycosidae, Psechridae and Thomisidae), affirming previous findings on the uncertain relationships of the "ctenids" Ancylometes and Cupiennius, although a core group of Ctenidae are well supported. Our data were ambiguous as to the monophyly of Oxyopidae. In Dionycha, we found a first split of core Prodidomidae, excluding the Australian Molycriinae, which fall distantly from core prodidomids, among gnaphosoids. The rest of the dionychans form two main groups, Dionycha part A and part B. The former includes much of the Oblique Median Tapetum clade (Trochanteriidae, Gnaphosidae, Gallieniellidae, Phrurolithidae, Trachelidae, Gnaphosidae, Ammoxenidae, Lamponidae and the Molycriinae), and also Anyphaenidae and Clubionidae. Orthobula is transferred from Phrurolithidae to Trachelidae. Our data did not allow for complete resolution for the gnaphosoid families. Dionycha part B includes the families Salticidae, Eutichuridae, Miturgidae, Philodromidae, Viridasiidae, Selenopidae, Corinnidae and Xenoctenidae (new fam., including Xenoctenus, Paravulsor and Odo, transferred from Miturgidae, as well as Incasoctenus from Ctenidae). We confirm the inclusion of Zora (formerly Zoridae) within Miturgidae.

A new epigean harvestman of the genus Guerrobunus (Laniatores: Phalangodidae), from Hidalgo, Mexico, with taxonomic notes about the genus.

The fifth species of the genus Guerrobunus, Guerrobunus barralesi sp. nov. is described from specimens collected in Hidalgo, Mexico. This species represents the first eastern record from the country and unlike other species of the genus, is completely epigean. Guerrobunus barralesi sp. nov. is compared with the most similar species, Guerrobunus minutus, which also has well developed and pigmented eyes. Finally, external morphology, including male genitalia, taxonomy of the genus, and familial assignment into the family Phalangodidae are discussed.

A new cavernicolous harvestman, Texella martensi n. sp., from the Mojave Desert, California (Opiliones: Laniatores: Phalangodidae).

A new species of Texella, T. martensi n. sp., is described on the basis of a single male specimen from Titus Canyon Cave, Inyo County, California. The species belongs to the kokoweef group in having a spur on trochanter IV and lacking a postopercular process on the abdomen. Texella martensi n. sp. is the most troglomorphic of the four species of Texella now recorded from the Mojave Desert and it is the northernmost member of the group.

New and unusual host records for North American and South American spider wasps (Hymenoptera: Pompilidae).

New and unusual host records for 133 species and subspecies of Pompilidae predominantly from the southwestern United States, Mexico, Central America, and South America are presented in modified taxonomic order. First-time species host records are given for Calopompilus Ashmead, Pepsis Fabricius, Hemipepsis Dahlbom, Priocnessus Banks, Entypus Dahlbom, Pompilocalus Roig-Alsina, Sphictostethus Kohl, Auplopus Spinola, Ageniella Banks, Eragenia Banks, Aporus Spinola, Poecilopompilus Ashmead, Tachypompilus Ashmead, Anoplius Dufour, Priochilus (Fabricius) and Notocyphus Smith. New host spider families are introduced for Calopompilus, Pepsis, Hemipepsis, Priocnessus, Entypus, Cryptocheilus Panzer, Priocnemis Schiødte, Auplopus, Ageniella, Eragenia, Aporus, Tachypompilus, Anoplius, Priochilus and Notocyphus. Eight host spider families are reported from the Western Hemisphere for the first time: Halonoproctidae (Notocyphus dorsalis dorsalis Cresson); Dipluridae (Pepsis pretiosa Dahlbom, P. montezuma Smith, P. infuscate Spinola, P. atripennis Fabricius, P. martini Vardy, Priocnessus vancei Waichert and Pitts); Nemesiidae (Pepsis pallidolimbata Lucas, P. viridis Lepeletier, P. spp., Pompilocalus hirticeps (Guérin), Sphictostethus gravesii (Haliday), S. striatulus Roig-Alsina, Priocnemis oregona Banks); Barychelidae (Eragenia sp.); Paratropididae (Pepsis stella Montet); Trechaleidae (Hemipepsis toussainti (Banks), Entypus unifasciatus cressoni (Banks), Tachypompilus ferrugineus (Say), Tachypompilus unicolor cerinus Evans, Priochilus gloriosum (Cresson); Desidae (Ageniella accepta (Cresson), Sphictostethus isodontus Roig-Alsina) and Selenopidae (Priochilus scrupulum (Fox), Tachypompilus erubescens (Taschenberg) or xanthopterus (Rohwer)). The first known host records for the rare South American pompilid genera Chirodamus (Lycosidae: Lycosa sp.) and Herbstellus (Nemesiidae: Diplothelopsis cf bonariensis Mello-Leitão) are presented.

A revision of the new world goblin spider genus Cinetomorpha Simon, 1892 revalidated from Gamasomorpha Karsch, 1881 (Araneae, Oonopidae, Oonopinae).

The goblin spider genus Cinetomorpha Simon is removed from the synonymy of Gamasomorpha Karsch and treated as the senior synonym of Yumates Chamberlin and Lucetia Dumitresco Georgesco. All 41 species occur only in the New World, and the genus is divided into four species groups: the simplex group, the puberula group, the patquiana group and the itabaiana group. The following species are transferred to Cinetomorpha: C. floridana (Banks), comb. nov., and C. sedata (Gertsch Mulaik), comb. nov., from Opopaea; C. angela (Chamberlin), comb. nov., and C. nesophila (Chamberlin), comb. nov., from Yumates; and C. patquiana (Birabén) and C. platensis (Birabén), comb. nov., from Gamasomorpha. Gamasomorpha wasmanniae Mello-Leitão and Lucetia distincta Dumitresco Georgesco are newly synonymized with C. simplex Simon. Two species currently in Gamasomorpha are transferred to Hexapopha Platnick Berniker: H. brasiliana (Bristowe), comb. nov. and H. m-scripta (Birabén), comb. nov. The following 31 species are newly described: C. adaga Ott Bonaldo (Brazil, Colombia, Ecuador and Peru); C. atlantica Ott Brescovit (Brazil); C. baja Ott Ubick (Mexico); C. bandolera Ott Harvey (Mexico USA); C. boraceia Ott Brescovit (Argentina and Brazil); C. campana Ott Harvey (Chile); C. central Ott Brescovit (Brazil); C. chicote Ott Bonaldo (Brazil, Colombia, Ecuador and Peru); C. concepcion Ott Harvey (Chile); C. iguazu Ott Brescovit (Argentina and Brazil); C. itabaiana Ott Brescovit (Brazil); C. laguna Ott Ubick (Mexico); C. lavras Ott Brescovit (Brazil); C. longisetosa Ott Harvey (Costa Rica and Brazil); C. lorenzo Ott Harvey (Guatemala); C. loreto Ott Bonaldo (Peru); C. nayarit Ott Harvey (Mexico); C. orellana Ott Bonaldo (Ecuador); C. pauferro Ott Brescovit (Brazil); C. peluda Ott Harvey (Chile); C. pinheiral Ott Brescovit (Brazil); C. pocone Ott Brescovit (Brazil); C. punctata Ott Brescovit (Brazil); C. quillota Ott Harvey (Chile); C. rinconada Ott Harvey (Chile); C. santamaria Ott Brescovit (Argentina); C. similis Ott Brescovit (Brazil); C. sternalis Ott Bonaldo (Brazil); C. sur Ott Ubick (Mexico); C. waorani Ott Bonaldo (Ecuador); and C. zero Ott Harvey (Mexico to Venezuela).

A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements.

Molecular phylogenetics has transitioned into the phylogenomic era, with data derived from next-generation sequencing technologies allowing unprecedented phylogenetic resolution in all animal groups, including understudied invertebrate taxa. Within the most diverse harvestmen suborder, Laniatores, most relationships at all taxonomic levels have yet to be explored from a phylogenomics perspective. Travunioidea is an early-diverging lineage of laniatorean harvestmen with a Laurasian distribution, with species distributed in eastern Asia, eastern and western North America, and south-central Europe. This clade has had a challenging taxonomic history, but the current classification consists of ~77 species in three families, the Travuniidae, Paranonychidae, and Nippononychidae. Travunioidea classification has traditionally been based on structure of the tarsal claws of the hind legs. However, it is now clear that tarsal claw structure is a poor taxonomic character due to homoplasy at all taxonomic levels. Here, we utilize DNA sequences derived from capture of ultraconserved elements (UCEs) to reconstruct travunioid relationships. Data matrices consisting of 317-677 loci were used in maximum likelihood, Bayesian, and species tree analyses. Resulting phylogenies recover four consistent and highly supported clades; the phylogenetic position and taxonomic status of the enigmatic genus Yuria is less certain. Based on the resulting phylogenies, a revision of Travunioidea is proposed, now consisting of the Travuniidae, Cladonychiidae, Paranonychidae (Nippononychidae is synonymized), and the new family Cryptomastridae Derkarabetian & Hedin, fam. n., diagnosed here. The phylogenetic utility and diagnostic features of the intestinal complex and male genitalia are discussed in light of phylogenomic results, and the inappropriateness of the tarsal claw in diagnosing higher-level taxa is further corroborated.

A revision of the new world goblin spider genus Cinetomorpha Simon, 1892 revalidated from Gamasomorpha Karsch, 1881 (Araneae, Oonopidae, Oonopinae)

The goblin spider genus Cinetomorpha Simon is removed from the synonymy of Gamasomorpha Karsch and treated as the senior synonym of Yumates Chamberlin and Lucetia Dumitresco & Georgesco. All 41 species occur only in the New World, and the genus is divided into four species groups: the simplex group, the puberula group, the patquiana group and the itabaiana group. The following species are transferred to Cinetomorpha: C. floridana (Banks), comb. nov., and C. sedata (Gertsch & Mulaik), comb. nov., from Opopaea; C. angela (Chamberlin), comb. nov., and C. nesophila (Chamberlin), comb. nov., from Yumates; and C. patquiana (Birabén) and C. platensis (Birabén), comb. nov., from Gamasomorpha. Gamasomorpha wasmanniae Mello-Leitão and Lucetia distincta Dumitresco & Georgesco are newly synonymized with C. simplex Simon. Two species currently in Gamasomorpha are transferred to Hexapopha Platnick & Berniker: H. brasiliana (Bristowe), comb. nov. and H. m-scripta (Birabén), comb. nov. The following 31 species are newly described: C. adaga Ott & Bonaldo (Brazil, Colombia, Ecuador and Peru); C. atlantica Ott & Brescovit (Brazil); C. baja Ott & Ubick (Mexico); C. bandolera Ott & Harvey (Mexico & USA); C. boraceia Ott & Brescovit (Argentina and Brazil); C. campana Ott & Harvey (Chile); C. central Ott & Brescovit (Brazil); C. chicote Ott & Bonaldo (Brazil, Colombia, Ecuador and Peru); C. concepcion Ott & Harvey (Chile); C. iguazu Ott & Brescovit (Argentina and Brazil); C. itabaiana Ott & Brescovit (Brazil); C. laguna Ott & Ubick (Mexico); C. lavras Ott & Brescovit (Brazil); C. longisetosa Ott & Harvey (Costa Rica and Brazil); C. lorenzo Ott & Harvey (Guatemala); C. loreto Ott & Bonaldo (Peru); C. nayarit Ott & Harvey (Mexico); C. orellana Ott & Bonaldo (Ecuador); C. pauferro Ott & Brescovit (Brazil); C. peluda Ott & Harvey (Chile); C. pinheiral Ott & Brescovit (Brazil); C. pocone Ott & Brescovit (Brazil); C. punctata Ott & Brescovit (Brazil); C. quillota Ott & Harvey (Chile); C. rinconada Ott & Harvey (Chile); C. santamaria Ott & Brescovit (Argentina); C. similis Ott & Brescovit (Brazil); C. sternalis Ott & Bonaldo (Brazil); C. sur Ott & Ubick (Mexico); C. waorani Ott & Bonaldo (Ecuador); and C. zero Ott & Harvey (Mexico to Venezuela).

A revision of the new world goblin spider genus Cinetomorpha Simon, 1892 revalidated from Gamasomorpha Karsch, 1881 (Araneae, Oonopidae, Oonopinae)

The goblin spider genus Cinetomorpha Simon is removed from the synonymy of Gamasomorpha Karsch and treated as the senior synonym of Yumates Chamberlin and Lucetia Dumitresco & Georgesco. All 41 species occur only in the New World, and the genus is divided into four species groups: the simplex group, the puberula group, the patquiana group and the itabaiana group. The following species are transferred to Cinetomorpha: C. floridana (Banks), comb. nov., and C. sedata (Gertsch & Mulaik), comb. nov., from Opopaea; C. angela (Chamberlin), comb. nov., and C. nesophila (Chamberlin), comb. nov., from Yumates; and C. patquiana (Birabén) and C. platensis (Birabén), comb. nov., from Gamasomorpha. Gamasomorpha wasmanniae Mello-Leitão and Lucetia distincta Dumitresco & Georgesco are newly synonymized with C. simplex Simon. Two species currently in Gamasomorpha are transferred to Hexapopha Platnick & Berniker: H. brasiliana (Bristowe), comb. nov. and H. m-scripta (Birabén), comb. nov. The following 31 species are newly described: C. adaga Ott & Bonaldo (Brazil, Colombia, Ecuador and Peru); C. atlantica Ott & Brescovit (Brazil); C. baja Ott & Ubick (Mexico); C. bandolera Ott & Harvey (Mexico & USA); C. boraceia Ott & Brescovit (Argentina and Brazil); C. campana Ott & Harvey (Chile); C. central Ott & Brescovit (Brazil); C. chicote Ott & Bonaldo (Brazil, Colombia, Ecuador and Peru); C. concepcion Ott & Harvey (Chile); C. iguazu Ott & Brescovit (Argentina and Brazil); C. itabaiana Ott & Brescovit (Brazil); C. laguna Ott & Ubick (Mexico); C. lavras Ott & Brescovit (Brazil); C. longisetosa Ott & Harvey (Costa Rica and Brazil); C. lorenzo Ott & Harvey (Guatemala); C. loreto Ott & Bonaldo (Peru); C. nayarit Ott & Harvey (Mexico); C. orellana Ott & Bonaldo (Ecuador); C. pauferro Ott & Brescovit (Brazil); C. peluda Ott & Harvey (Chile); C. pinheiral Ott & Brescovit (Brazil); C. pocone Ott & Brescovit (Brazil); C. punctata Ott & Brescovit (Brazil); C. quillota Ott & Harvey (Chile); C. rinconada Ott & Harvey (Chile); C. santamaria Ott & Brescovit (Argentina); C. similis Ott & Brescovit (Brazil); C. sternalis Ott & Bonaldo (Brazil); C. sur Ott & Ubick (Mexico); C. waorani Ott & Bonaldo (Ecuador); and C. zero Ott & Harvey (Mexico to Venezuela).

The spider tree of life: phylogeny of Araneae based on target-gene analyses from an extensive taxon sampling

We present a phylogenetic analysis of spiders using a dataset of 932 spider species, representing 115 families (only the family Synaphridae is unrepresented), 700 known genera, and additional representatives of 26 unidentified or undescribed genera. Eleven genera of the orders Amblypygi, Palpigradi, Schizomida and Uropygi are included as outgroups. The dataset includes six markers from the mitochondrial (12S, 16S, COI) and nuclear (histone H3, 18S, 28S) genomes, and was analysed by multiple methods, including constrained analyses using a highly supported backbone tree from transcriptomic data. We recover most of the higher-level structure of the spider tree with good support, including Mesothelae, Opisthothelae, Mygalomorphae and Araneomorphae. Several of our analyses recover Hypochilidae and Filistatidae as sister groups, as suggested by previous transcriptomic analyses. The Synspermiata are robustly supported, and the families Trogloraptoridae and Caponiidae are found as sister to the Dysderoidea. Our results support the Lost Tracheae clade, including Pholcidae, Tetrablemmidae, Diguetidae, Plectreuridae and the family Pacullidae (restored status) separate from Tetrablemmidae. The Scytodoidea include Ochyroceratidae along with Sicariidae, Scytodidae, Drymusidae and Periegopidae; our results are inconclusive about the separation of these last two families. We did not recover monophyletic Austrochiloidea and Leptonetidae, but our data suggest that both groups are more closely related to the Cylindrical Gland Spigot clade rather than to Synspermiata. Palpimanoidea is not recovered by our analyses, but also not strongly contradicted. We find support for Entelegynae and Oecobioidea (Oecobiidae plus Hersiliidae), and ambiguous placement of cribellate orb-weavers, compatible with their non-monophyly. Nicodamoidea (Nicodamidae plus Megadictynidae) and Araneoidea composition and relationships are consistent with recent analyses. We did not obtain resolution for the titanoecoids (Titanoecidae and Phyxelididae), but the Retrolateral Tibial Apophysis clade is well supported. Penestomidae, and probably Homalonychidae, are part of Zodarioidea, although the latter family was set apart by recent transcriptomic analyses. Our data support a large group that we call the marronoid clade (including the families Amaurobiidae, Desidae, Dictynidae, Hahniidae, Stiphidiidae, Agelenidae and Toxopidae). The circumscription of most marronoid families is redefined here. Amaurobiidae include the Amaurobiinae and provisionally Macrobuninae. We transfer Malenellinae (Malenella, from Anyphaenidae), Chummidae (Chumma) (new syn.) and Tasmarubriinae (Tasmarubrius, Tasmabrochus and Teeatta, from Amphinectidae) to Macrobuninae. Cybaeidae are redefined to include Calymmaria, Cryphoeca, Ethobuella and Willisius (transferred from Hahniidae), and Blabomma and Yorima (transferred from Dictynidae). Cycloctenidae are redefined to include Orepukia (transferred from Agelenidae) and Pakeha and Paravoca (transferred from Amaurobiidae). Desidae are redefined to include five subfamilies: Amphinectinae, with Amphinecta, Mamoea, Maniho, Paramamoea and Rangitata (transferred from Amphinectidae); Ischaleinae, with Bakala and Manjala (transferred from Amaurobiidae) and Ischalea (transferred from Stiphidiidae); Metaltellinae, with Austmusia, Buyina, Calacadia, Cunnawarra, Jalkaraburra, Keera, Magua, Metaltella, Penaoola and Quemusia; Porteriinae (new rank), with Baiami, Cambridgea, Corasoides and Nanocambridgea (transferred from Stiphidiidae); and Desinae, with Desis, and provisionally Poaka (transferred from Amaurobiidae) and Barahna (transferred from Stiphidiidae). Argyroneta is transferred from Cybaeidae to Dictynidae. Cicurina is transferred from Dictynidae to Hahniidae. The genera Neoramia (from Agelenidae) and Aorangia, Marplesia and Neolana (from Amphinectidae) are transferred to Stiphidiidae. The family Toxopidae (restored status) includes two subfamilies: Myroinae, with Gasparia, Gohia, Hulua, Neomyro, Myro, Ommatauxesis and Otagoa (transferred from Desidae); and Toxopinae, with Midgee and Jamara, formerly Midgeeinae, new syn. (transferred from Amaurobiidae) and Hapona, Laestrygones, Lamina, Toxops and Toxopsoides (transferred from Desidae). We obtain a monophyletic Oval Calamistrum clade and Dionycha; Sparassidae, however, are not dionychans, but probably the sister group of those two clades. The composition of the Oval Calamistrum clade is confirmed (including Zoropsidae, Udubidae, Ctenidae, Oxyopidae, Senoculidae, Pisauridae, Trechaleidae, Lycosidae, Psechridae and Thomisidae), affirming previous findings on the uncertain relationships of the "ctenids" Ancylometes and Cupiennius, although a core group of Ctenidae are well supported. Our data were ambiguous as to the monophyly of Oxyopidae. In Dionycha, we found a first split of core Prodidomidae, excluding the Australian Molycriinae, which fall distantly from core prodidomids, among gnaphosoids. The rest of the dionychans form two main groups, Dionycha part A and part B. The former includes much of the Oblique Median Tapetum clade (Trochanteriidae, Gnaphosidae, Gallieniellidae, Phrurolithidae, Trachelidae, Gnaphosidae, Ammoxenidae, Lamponidae and the Molycriinae), and also Anyphaenidae and Clubionidae. Orthobula is transferred from Phrurolithidae to Trachelidae. Our data did not allow for complete resolution for the gnaphosoid families. Dionycha part B includes the families Salticidae, Eutichuridae, Miturgidae, Philodromidae, Viridasiidae, Selenopidae, Corinnidae and Xenoctenidae (new fam., including Xenoctenus, Paravulsor and Odo, transferred from Miturgidae, as well as Incasoctenus from Ctenidae). We confirm the inclusion of Zora (formerly Zoridae) within Miturgidae.