@article {8631, title = {Hunting the wolf: a molecular phylogeny of the wolf spiders (Araneae, Lycosidae)}, journal = {Molecular Phylogenetics and Evolution}, volume = {136}, year = {2019}, pages = {227-240}, author = {Piacentini, Luis N. and Ram{\'\i}rez, Mart{\'\i}n J} } @article {8582, title = {A revision of the American spider genus Strotarchus Simon, 1888 (Araneae: Dionycha, Systariinae).}, journal = {Zootaxa}, volume = {3363:}, year = {2012}, pages = {1-37}, author = {Bonaldo, Alexandre and Saturnino, Regiane and Ram{\'\i}rez, Mart{\'\i}n J and Brescovit, Antonio D} } @article {8580, title = {The Crevice Weaver Spider Genus Kukulcania (Araneae: Filistatidae)}, journal = {Bulletin of the American Museum of Natural History}, volume = {2019}, year = {2019}, pages = {1 - 151}, abstract = {

Filistatidae is one of the most phylogenetically enigmatic spider groups, and the genus Kukulcania Lehtinen includes the commonest representatives of the family. Its type species, K. hibernalis (Hentz, 1842), remains a favorite candidate for studies on spider phylogeny and comparative morphology. However, little is known about the taxonomy, species limits, and distribution of its closest relatives, because no generic revision has ever been undertaken. We present the first comprehensive assessment of the taxonomy of Kukulcania. The species K. hibernalis, K. arizonica (Chamberlin and Ivie, 1935), K. utahana (Chamberlin and Ivie, 1935), K. hurca (Chamberlin and Ivie, 1942), K. brignolii (Alay\ón, 1981) comb. nov. (transferred here from Filistata Latreille), K. tractans (O. Pickard-Cambridge, 1896), and K. geophila (Chamberlin and Ivie, 1935) are redescribed based on our examination of type material. We show that the name Filistata brevipesKeyserling, 1883, which had previously been placed in Kukulcania, actually belongs to a prithine spider, and propose the new combination Pikelinia brevipes (Keyserling, 1883). Filistata geophila wawona Chamberlin and Ivie, 1942, is newly synonymized with Kukulcania geophila. Eight new species of Kukulcania are described: K. cochimi, sp. nov. (from Baja California), K. gertschi, sp. nov. (northern Mexico), K. mexicana, sp. nov. (central Mexico), K. santosi, sp. nov. (southern Mexico to northern South America; previously misidentified as K. brevipes), K. tequila, sp. nov. (western Mexico), K. chingona, sp. nov. (western Mexico), K. benita, sp. nov. (endemic to the San Benito Islands in Baja California) and K. bajacali, sp. nov. (Baja California). With this, the number of recognized species in the genus is increased to 15. All species have their distributions mapped and both sexes illustrated. The first identification key to the genus is presented. A study on the morphology of the genus is undertaken using light and scanning electron microscopy, and the phylogenetic position of Kukulcania within the Filistatinae is briefly discussed. A novel putative synapomorphy for the subfamily is proposed

}, doi = {10.1206/00030090-426.1.1}, url = {https://doi.org/10.1206/00030090-426.1.1}, author = {Magalhaes, Ivan L F and Ram{\'\i}rez, Mart{\'\i}n J} } @article {8524, title = {Courtship, egg sac construction, and maternal care in Kukulcania hibernalis, with information on the courtship of Misionella mendensis (Araneae, Filistatidae)}, journal = {Arachnology}, volume = {16}, year = {2013}, pages = {72-80}, author = {Barrantes, Gilbert and Ram{\'\i}rez, Mart{\'\i}n J} } @article {8497, title = {Taxonomic revision of the jumping goblin spiders of the genus Orchestina Simon, 1882, in the Americas (Araneae, Oonopidae).}, journal = {Bulletin of the American Museum of Natural History}, volume = {410}, year = {2017}, pages = {1-162}, abstract = {

The genus Orchestina Simon is distributed worldwide and is characterized by having an enlarged fourth femur with which these species are capable of jumping. The genus is also characterized by having a well-sclerotized sperm duct, a near H-shaped arrangement of the eye group, a 4-4-3-3 pattern of raised receptors on the tarsal organs of the legs I-IV, respectively, and by lacking spines on all the legs. All these characters, together with molecular evidence, support the monophyly of the genus, as well as its placement as sister group of Oonopinae. Most American species of Orchestina inhabit the forest foliage and canopy, but in unforested areas they also occur in shrubs and grasses. In this work, we revise the American representatives of Orchestina in a comprehensive context for the first time. In the past, six species were known from the Americas: five from the United States and only one from South America, described from Venezuela. After the study of the principal collections of the world and several field trips to several South American countries, we describe 85 new species and redescribe all previously known species. Matching sexes was occasionally problematic; while females are very homogeneous in somatic traits, males may have modifications on different parts of the body, making the matching very difficult. Therefore, in this review 56 of the species are described from only one sex, whereas 20 unmatched species are informally described as morphospecies, pending the discovery of conspecific sexes. Two species, O. pavesiiformis Saaristo and O. dentifera Simon, originally known from Israel and Sri Lanka, respectively, are here reported as introduced in several countries in the Americas and other continents. O. justini Saaristo described from the Seychelles is here considered a synonym of O. dentifera. One species, O. truncata Wunderlich, previously known as a subfossil spider from Colombian copal is here tentatively redescribed based on recent material from Costa Rica, Colombia, and Ecuador; the female is also described for the first time. The species list by country is as follows (numbers refer to records, independently of the locality of the type material): United States (9 species: O. utahana Chamberlin and Ivie, O. moaba Chamberlin and Ivie, O. obscura Chamberlin and Ivie, O. saltitans Banks, O. nadleri Chickering, the introduced O. pavesiiformis Saaristo, and three new species, O. quasimodo, O. kamehameha, and O. auburndalensis); Mexico (3 species: O. utahana Chamberlin and Ivie, and two new species, O. nahuatl and O. chaparrita); Guatemala (1 new species: O. guatemala); Costa Rica (3 new species: O. laselva, O. griswoldi, and O. chiriqui; and the previously known O. truncata Wunderlich); Panama (5 new species: O. chiriqui, O. labarquei, O. pan, O. campana, and O. galapagos); Jamaica (2 species, the introduced O. dentifera Simon and O. galapagos); Haiti and Dominican Republic (only the introduced O. dentifera Simon); Colombia (6 new species: O. filandia, O. zingara, O. arboleda, O. cali, O. platnicki, O. pakitza; and O. truncata Wunderlich, plus the morphospecies OMI020 and OMI038); Venezuela (7 species: O. saltabunda; and 6 new, O. venezuela, O. aragua, O. bolivar, O. maracay, O. ranchogrande, and O. neblina); Trinidad and Tobago (1 new species: O. kairi); Guyana (1 morphospecies: OMI026); Ecuador (18 new species: O. galapagos, O. fernandina, O. erwini, O. ecuatoriensis, O. sotoi, O. magna, O. shuar, O. golem, O. waorani, O. tzantza, O. predator, O. goblin, O. yanayacu, O. otonga, O. santodomingo, O. quijos, O. mayo, O. laselva, and O. truncata Wunderlich, plus the morphospecies OMI020, OMI021, OMI022, OMI023, OMI024, OMI025, OMI026, OMI027, OMI029, OMI036, and OMI038); Peru (9 new species: O. cajamarca, O. comaina, O. atocongo, O. mancocapac, O. silvae, O. madrededios, O. pakitza, O. losamigos, O. golem, and the morphospecies OMI020, OMI023, OMI026, and OMI030); Brazil (25 new species: O. cristinae, O. coari, O. moura, O. valquiria, O. aproeste, O. caxiuana, O. para, O. taruma, O. retiro, O. divisor, O. juruti, O. platnicki, O. iemanja, O. bonaldoi, O. rapaz, O. itapety, O. catarina, O. leon, O. saudade, O. sarava, O. goblin, O. sotoi, O. golem, O. waorani, O. ucumar, the introduced O. pavesiiformis Saaristo, and O. dentifera Simon, plus the morphospecies OMI021, OMI023, OMI024, OMI025, OMI026, OMI027, OMI029, OMI032, OMI033, OMI034, OMI035, OMI036, OMI037, OMI039, and OMI040); Bolivia (3 new species: O. moyuchi, O. grismadoi, and O. ucumar); Chile (12 new species: O. pandeazucar, O. caleta, O. totoralillo, O. pizarroi, O. molles, O. granizo, O. quenies, O. curico, O. cachai, O. nahuelbuta, O. jaiba, and O. osorno); and Argentina (6 new species: O. ucumar, O. andianavarroi, O. luispi, O. cristinae, O. platnicki, O. jaiba, and the introduced O. pavesiiformis Saaristo). Although the internal relationships of the genus are still not clear, we suggest some groups of species based on morphological characters and geographic distributions. Species from the western United States share the presence of a net-shaped pattern of coloration and, in some species, modifications of carapace or first legs of males. Females of this group are characterized by the presence of a thin, generally long and twisted anterior receptaculum and external pockets on the epigastric region. This group inhabits in a geographic region that remained isolated during the late Cretaceous and is still isolated by geographic and climatic conditions. Species groups in South American members were more difficult to establish, given their wide diversity. However, some species are unique in having internal pockets in female genitalia and apophyses on the male copulatory bulb. The Chilean species are probably a monophyletic group; they are separated from the rest by the combined presence of external pockets and ridges on the epigastric region of female, whereas males are very similar in the morphology of copulatory bulb, which is very simple, with long embolus and sometimes with additional spine-shaped apophysis. This group may have experienced events of isolation during and after the elevation of the Andes range. As in other members of the family the genus is interesting for the presence of secondary sexual characters in males whereas females are practically homogenous in somatic characters. However, female genital morphology is variable, which may suggest a coevolution with somatic characters in males and probably mechanical interactions. Although this work reveals the incredible diversity of this genus, many important geographic regions remain undersampled and records for some countries are entirely lacking.

}, url = {http://digitallibrary.amnh.org/handle/2246/6699}, author = {Izquierdo, Mat{\'\i}as A and Ram{\'\i}rez, Mart{\'\i}n J} } @article {8104, title = {The world goblin spiders of the new genus Neotrops (Araneae: Oonopidae), part 1}, journal = {Bulletin of the American Museum of Natural History}, volume = {383}, year = {2013}, pages = {1-150}, abstract = {

A new genus of soft-bodied oonopids, Neotrops, is established for a large assemblage of goblin spiders found in all tropical and subtropical areas of the Neotropical region, from Panama to Uruguay and central Argentina. Members of Neotrops have spinose forelegs, and share a general palpal morphology with those of Heteroonops Dalmas, but have a prolateral conductor connected with an internal bulbal vesicle that presumably discharges its secretion through a prolateral slit. Females lack a posterior receptacle in the internal genitalia, having only a posterodorsal plate serving for muscle attachment. Here we treat all the species except those from Brazil, which will be addressed in a subsequent paper. Twenty-three new species are described: N. darwini (type species), N. lorenae, and N. sciosciae (from Argentina and Uruguay); N. yunga, N. piacentinii, N. poguazu, and N. lopardoae (from Argentina); N. rubioi, N. pombero, and N. avalosi (from Argentina and Paraguay); N. labarquei (from Uruguay), N. yabare, N. izquierdoi, and N. kopuchianae (from Bolivia); N. pithecia, N. silvae, and N. pakitza (from Peru); N. platnicki, and N. waorani (from Ecuador); N. santamarta and N. caparu (from Colombia); and N. maracay and N. amacuro (from Venezuela). Four additional species, previously placed in Oonops Templeton, are transferred here to Neotrops: O. nigromaculatus Mello-Leita ̃o, from Argentina and Uruguay; O. tucumanus Simon, from Argentina; O. donaldi Chickering, from Panama; and O. trapellus Chickering, from Trinidad and Venezuela. The females of the three latter species are here described for the first time. Most of the species are known from the leaf litter or the foliage of tropical and subtropical forests, but also from grasslands in the southern parts of their distributional range, where they appear as the dominant soft-bodied oonopids. The relationships of this new taxon are briefly discussed, and intrageneric groupings are also proposed.

}, author = {Grismado, Christian J and Ram{\'\i}rez, Mart{\'\i}n J} } @article {8076, title = {The spider subfamily Amaurobioidinae (Araneae, Anyphaenidae): a phylogenetic revision at the generic level}, journal = {Bulletin of the American Museum of Natural History}, volume = {277}, year = {2003}, pages = {1-262}, abstract = {

A cladistic phylogenetic analysis at generic level of the subfamily Amaurobioidinae is presented. The analysis is based on a dataset of 93 representative species scored for one behavioral and 199 morphological characters. Tree searches were made under equal and implied weights according to homoplasy, and the results were compared in terms of sensitivity to jackknife resampling. Mildest weighting functions produced trees more robust to resampling, and those results were selected as the working phylogenetic hypotheses. Groups of weak support as identified by jackknifing and Bremer indices are in general those that vary in resolution with different character-weighting schemes.
Seven outgroup representatives were included (Malenella nana Raḿ{\i}rez, from Malenellinae, and six Anyphaeninae species). In this analysis Anyphaeninae, previously identified as sister group of Amaurobioidinae, is paraphyletic, but forcing its monophyly does not alter the groupings within Amaurobioidinae. The monophyly of the genera is in general well supported, but some particularly conflicting groups are discussed. In contrast, the relationships among genera are in general problematic.
Amaurobioidinae is diagnosed by a pronounced indentation at the base of male palpal tegulum, and by a particular male copulatory bulb conformation, with a paramedian apophysis. The subfamily is classified in two tribes (Gayennini and Amaurobioidini); the genus Josa Keyserling, probably sister group to Gayennini, is not assigned to either tribe.
The tribe Amaurobioidini is mainly diagnosed by an apical loop of the sperm duct in the male copulatory bulb. It includes 10 genera: Amaurobioides O.P.-Cambridge is restricted to seashores of southern continents. Clubiona chilensis Nicolet, transferred to Amaurobioides, is the first true record of the genus for South America. The male of Axyracrus elegans Simon, three species of Aysenia Tullgren, and three of Coptoprepes Simon are newly described. Four new genera are proposed in Amaurobioidini: Gamakia, Selknamia (described for one new species each), Aysenoides (for three new species), and Negayan (type species Gayenna tri- dentata Simon, including also Axyracrus coccineus Mello-Leita ̃o, Clubiona paduana Karsch, Gayenna excepta Tullgren, Gayenna exigua Mello-Leitão, and Tomopisthes lebruni Simon). The previously revised genera Acanthoceto Mello-Leitao and Ferrieria Tullgren are also in- cluded in the tribe. The basal branch and most intergeneric branches of the tribe have low support values. Amaurobioides and Negayan, however, are relatively well supported.
The tribe Gayennini is well defined by a homogeneous conformation of male and female genitalia, with a distinctive secondary conductor and spherical spermathecae. It includes 11 genera: Gayenna Nicolet includes only G. americana Nicolet from Chile and adjacent Argen- tina. Arachosia O.P.-Cambridge comprises many species previously assigned to Oxysoma. Abuzaida striata Keyserling, Anyphaena oblonga Keyserling, Gayenna proseni Mello-Leita ̃o, Gayenna duplovittata Mello-Leita ̃o, Gayenna bonneti Mello-Leita ̃o, Oxysoma dubium Berland, Oxysoma bifasciatum Mello-Leita ̃o, Oxysoma cubana Banks, Oxysoma polytrichium Mello- Leita ̃o, Phidyle bergi Simon, and Samuza praesignis Keyserling are transferred to Arachosia. The males of Arachosia bergi (Simon), A. honesta Keyserling, and Arachosia praesignis (Key- serling) are newly described. Arachosia is easily recognized by the thick setae on the anterior lateral spinnerets, and it has good support values. A very diverse group of species here as- signed to the genus Sanogasta Mello-Leita ̃o is paraphyletic in terms of Arachosia. It includes many of the species formerly placed in Gayenna Nicolet. Anyphaena maculatipes Keyserling, Clubiona maculosa Nicolet, Gayenna paucilineata Mello-Leitão, Gayenna alticola Simon, Gayenna bonariensis Mello-Leitao, Gayenna rufithorax Tullgren, Gayenna x-signata Keyser- ling, Gayenna approximata Tullgren, Samuza minuta Keyserling, and Tomopisthes backhauseni Simon are transferred to Sanogasta. The female of Sanogasta alticola (Simon), the males of S. x-signata (Keyserling) and S. approximata (Tullgren), and four species are newly described. The males of Monapia carolina Ram ́{\i}rez and Monapia angusta (Mello-Leita ̃o) are newly described. A new species of Oxysoma Nicolet from southern Brazil is described, and Gayenna saccata Tullgren is transferred to Oxysoma. Phidyle Simon is removed from the synonymy of Oxysoma Nicolet; the male of its only species Phidyle punctipes (Nicolet) is newly described. The genus Philisca Simon is redefined to include Liparotoma Simon. Clubiona tripunctata Nicolet and Clubiona gayi Nicolet are also transferred to Philisca. The male of Philisca hahni Simon and two species are newly described. The genus is reasonably supported, except for one basal species of questionable placement. Anyphaena punctata Keyserling, Gayenna fuscotaeniata Keyserling, Gayenna tripunctata Mello-Leitao, Gayenna reticulata Mello-Leitão, Gayenna taperae Mello-Leitao, Oxysoma quinquenotatum Simon, Oxysoma unipunctatum Simon, Oxysoma novum Mello-Leitao, Oxysoma lineatum Tullgren, and Tomopisthes frenatus Mello-Leitao are transferred to Tasata. The males of Tasata parcepunctata Simon, T. variolosa Mello-Leitao, and three species are newly described. Tasata albofasciata Mello-Leitão is transferred to Tupirinna Bonaldo, in the Corinnidae. Tomopisthes Simon includes only three species from Chile and adjacent Argentina. Clubiona horrenda Nicolet and Clubiona pusilla Nicolet are transferred to Tomopisthes. The male of Tomopisthes pusillus (Nicolet) is newly described. Two new genera are proposed in Gayennini: Araiya (Gayenna pallida Tullgren, type species and Gayenna coccinea Simon) and Gayennoides (for two new Chilean species).

The genus Josa Keyserling, distinguished by a femoral apophysis on the male palp, is extremely diverse in Andean cloud forests and tropical America. It is one of the better supported groups of the analysis. Anyphaena keyserlingi L. Koch, Gayenna andesiana Berland, Gayenna simoni Berland, Gayennella riveti Berland, Haptisus nigrifrons Simon, Haptisus analis Simon, Haptisus maurus Simon, Olbophthalmus lojensis Berland, Olbus personatus Simon, Olbus gounellei Simon, Tetromma luteum Keyserling, and Tomopisthes chazaliae Simon are transferred to Josa. The male of Josa riveti (Berland) and one species are newly described.\ The following names are newly synonymized: Cluilius Simon, with Amaurobioides O.P.- Cambridge; Schiapellia Mello-Leitao, with Axyracrus Simon; Schiapellia gerschmanni Mello Leitão and Amaurobioides boydi Forster, with Axyracrus elegans Simon; Tomopisthes magel- lanicus Simon and Gayenna strigosa Tullgren, with Clubiona (now Negayan) paduana Karsch; Tetromma Keyserling (preoccupied), Haptisus Simon, Olbophthalmus Simon, and Gayennella Berland, with Josa Keyserling; Anyphaena pilosa Keyserling and Gayenna riveti Berland, with Tetromma (now Josa) luteum Keyserling; Pelayo insignis Banks, with Haptisus (now Josa) nigrifrons Simon; Samuza Keyserling, Abuzaida Keyserling, and Gayennina Gertsch, with Arachosia O.P.-Cambridge; Tomopisthes tripunctatus Mello-Leitão, with Samuza (now Arachosia) praesignis Keyserling; Oxysoma ramboi Mello-Leitao, with Arachosia honesta Keyserling; Sanogasta intermedia Mello-Leitao, with Anyphaena (now Sanogasta) maculatipes Keyserling; Gayenna monticola Chamberlin, with Gayenna alticola Simon; Clubiona sternalis Nicolet, Anyphaena ignota Keyserling, Gayenna affinis Tullgren, Gayenna dubia Tullgren, Tomopisthes conspersus Simon, Tomopisthes modestus Simon, Tomopisthes taeniatus Simon, Gayenna skottsbergi Berland, and Tomopisthes injucundus Simon, with Clubiona (now Sanogasta) maculosa Nicolet; Tomopisthes kraepelini Simon, with Gayenna approximata Tullgren; Liparotoma Simon, with Philisca Simon; Philisca navarinensis Tullgren, with Philisca hahni Simon; Heteromma Karsch (preoccupied), with Tomopisthes Simon; Tomopisthes im- manis Simon, Heteromma fuegiana Karsch, Philisca sica Strand, and Nonianus argentinus Mello-Leitao, with Clubiona (now Tomopisthes) horrenda Nicolet; Gayenna chilensis Tullgren, with Clubiona (now Tomopisthes) pusilla Nicolet; Gayenna stellata Simon, with Gayenna (now Araiya) coccinea Simon; Oxysoma punctipes Nicolet, Oxysoma aurata Nicolet, Oxysoma longipes Nicolet, Oxysoma lineata Nicolet, and Aporatea valdiviensis Simon, with Oxysoma punctatum Nicolet.
The following names, previously listed in Anyphaenidae, are considered nomina dubia: Anyphaena pampa Holmberg, Clubiona albiventris Nicolet, Clubiona citrina Nicolet, Clubiona gemella Nicolet, Clubiona gibbosa Nicolet, Clubiona lepida Nicolet, Clubiona limbata Nicolet, Clubiona lineata Nicolet, Clubiona nigricans Nicolet, Clubiona nubes Nicolet, Clubiona pulchella Nicolet, Clubiona puella Nicolet, Clubiona versicolor Nicolet, Oxysoma auratum Nicolet, Oxysoma delfini Simon, and Tomopisthes aethiops Simon.

}, author = {Ram{\'\i}rez, Mart{\'\i}n J} } @article {572, title = {The morphology and phylogeny of dionychan spiders (Araneae: Arameomorphae)}, journal = {Bulletin of the American Museum of Natural History}, year = {2014}, pages = {1-374}, abstract = {

A phylogenetic analysis of the two-clawed spiders grouped in Dionycha is presented, with 166 representative species of 49 araneomorph families, scored for 393 characters documented through standardized imaging protocols. The study includes 44 outgroup representatives of the main clades of Araneomorphae, and a revision of the main morphological character systems. Novel terminology is proposed for stereotyped structures on the chelicerae, and the main types of setae and silk spigots are reviewed, summarizing their characteristics. Clear homologs of posterior book lungs are described for early instars of Filistatidae, and a novel type of respiratory structure, the epigastric median tracheae, is described for some terminals probably related with Anyphaenidae or Eutichuridae. A new type of crypsis mechanism is described for a clade of thomisids, which in addition to retaining soil particles, grow fungi on their cuticle. Generalized patterns of cheliceral setae and macrosetae are proposed as synapomorphies of the Divided Cribellum and RTA clades. Dionycha is here proposed as a member of the Oval Calamistrum clade among the lycosoid lineages, and Liocranoides, with three claws and claw tufts, is obtained as a plausible sister group of the dionychan lineage. The morphology of the claw tuft and scopula is examined in detail and scored for 14 characters highly informative for relationships. A kind of seta intermediate between tenent and plumose setae (the pseudotenent type) is found in several spider families, more often reconstructed as a derivation from true tenent setae rather than as a phylogenetic intermediate. Corinnidae is retrieved in a restricted sense, including only the subfamilies Corinninae and Castianeirinae, while the \‘\‘corinnid\’\’ genera retaining the median apophysis in the copulatory bulb are not clearly affiliated to any of the established families. Miturgidae is redefined, including Zoridae as a junior synonym. The Eutichuridae is raised to family status, as well as the Trachelidae and Phrurolithidae. New synapomorphies are provided for Sparassidae, Philodromidae, and Trachelidae. Philodromidae is presented as a plausible sister group of Salticidae, and these sister to Thomisidae; an alternative resolution placing thomisids in Lycosoidea is also examined. The Oblique Median Tapetum (OMT) clade is proposed for a large group of families including gnaphosoids, trachelids, liocranids, and phrurolithids, all having the posterior median eye tapeta forming a 90u angle, used for navigation by means of the polarized light in the sky as an optical compass; prodidomines seem to have further enhanced the mechanism by incorporating the posterior lateral eyes to the system. The Teutamus group is recognized for members of the OMT clade that are usually included in Liocranidae, but not closely related to Liocranum or phrurolithids. The Claw Tuft Clasper (CTC) clade is proposed for a group of families within the OMT clade, all having a peculiar mechanism grasping the folded base of the claw tuft setae with a hook on the superior claws. The CTC clade includes Trachelidae, Phrurolithidae, and several gnaphosoids such as Ammoxenidae, Cithaeronidae, Gnaphosidae, and Prodidomidae. A remarkable syndrome involving the expansion of the anterior lateral spinnerets, often sexually dimorphic, is here reported for some Miturgidae and several members of the CTC clade, in addition to the known cases in Clubionidae and \‘\‘Liocranidae.\’\’ The following genera are transferred from Miturgidae to Eutichuridae: Calamoneta, Calamopus, Cheiracanthium, Cheiramiona, Ericaella, Eutichurus, Macerio, Radulphius, Strotarchus, Summacanthium, and Tecution; Lessertina is transferred from Corinnidae to Eutichuridae. The following genera are transferred to Miturgidae: Argoctenus, Elassoctenus, Hestimodema, Hoedillus, Israzorides, Odomasta, Simonus, Thasyraea, Tuxoctenus, Voraptus, Xenoctenus, Zora, and Zoroides, from Zoridae; Odo and Paravulsor, from Ctenidae; Pseudoceto from Corinnidae. The following genera are transferred from Corinnidae to Trachelidae: Afroceto, Cetonana, Fuchiba, Fuchibotulus, Meriola, Metatrachelas, Paccius, Paratrachelas, Patelloceto, Planochelas, Poachelas, Spinotrachelas, Thysanina, Trachelas, Trachelopachys, and Utivarachna. The following genera are transferred from Corinnidae to Phrurolithidae: Abdosetae, Drassinella, Liophrurillus, Plynnon, Orthobula, Otacilia, Phonotimpus, Phrurolinillus, Phrurolithus, Phruronellus, Phrurotimpus, Piabuna, and Scotinella. Dorymetaecus is transferred from Clubionidae to Phrurolithidae. Oedignatha and Koppe are transferred from Corinnidae to Liocranidae. Ciniflella is transferred from Amaurobiidae to Tengellidae.

}, url = {NOTE: SOME INTERNAL LINKS TO SPECIFIC TAXA TO ADD TO FILE}, author = {Ram{\'\i}rez, Mart{\'\i}n J} }