A revised phylogenetic analysis for the spider genus Clitaetra Simon, 1889 (Araneae, Araneoidea, Nephilidae) with the first description of the male of the Sri Lankan species Clitaetra thisbe Simon, 1903 PDF Download

Author: Dimitar Dimitrov
Publisher:
ISBN:
Category : Clitaetra
Languages : en
Pages : 23

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Author: Dimităr Dimitrov
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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Author: Eduardo M. Soto
Publisher:
ISBN: 9781869779948
Category : Anyphaenidae
Languages : en
Pages : 65

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We review the spider genus Philisca Simon, an endemic of the southern forests in Chile and Argentina, and present a phylogenetic analysis including 15 species, of which five are newly described (P. atrata, P. robinson, P. viernes, P. pizarroi and P. robusta), together with other 98 representatives of the family Anyphaenidae. Four species names are considered nomina dubia (Clubiona gayi Nicolet, Drassus mirandus Nicolet, Clubiona altiformis Nicolet, P. obscura Simon). Cluilius chilensis Mello-Leitão is newly synonymized with P. accentifera Simon. The phylogenetic analysis resulted in P. puconensis Ramírez branching off basally in the genus, because of its numerous leg spines and unmodified male chelicerae, all plesiomorphic for the group; the remaining species form two clear groups. The first one, formed by P. hahni Simon, P. tripunctata (Nicolet), P. amoena (Simon), P. hyadesi (Simon) and P. doilu (Ramírez), are grouped by the loss of spines on legs I and II. The second, formed by P. huapi Ramírez, P. ingens Berland, P. ornata Berland, P. accentifera Simon, P. atrata and four new species endemic to the Robinson Crusoe Island in the Juan Fernández Archipelago, have the male chelicerae, and in most cases also the endites, modified. In total, six species of Philisca are endemic to Juan Fernández, but our dataset is not conclusive for the distinction of alternative colonization scenarios. We analyze the evolution of leg macrosetae, and show two independent instances of reduction of spination, one on the continent and another on the Juan Fernández islands.

Author: Mihael G. Rix
Publisher: PenSoft Publishers LTD
ISBN: 9546425311
Category : Science
Languages : en
Pages : 328

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The Micropholcommatidae are a family of tiny, distinctive araneoid spiders, known from southern-temperate habitats throughout Australasia and Chile. The greatest abundance of individuals and the largest diversity of taxa occur in the cool-temperate rainforests of south-eastern Australia and New Zealand, where micropholcommatid spiders can be very common within moss and leaf litter microhabitats. Although poorly studied biologically and largely neglected taxonomically, the Micropholcommatidae are a diverse lineage, with a significantÿ The monograph in this volume presents a complete generic-level revision of the spider family Micropholcommatidae. The phylogenetic position and internal phylogeny of the family are tested with two separate morphological cladistic analyses, the results of which inform a comprehensive generic-level classification. In total, 26 new species, 12 new genera, one new tribe and two new subfamilies are described, taking the total documented micropholcommatid fauna to 58 species. The distribution and Gondwanan biogeography of the family are also discussed, and natural history information is provided where known. Most importantly, the results of this paper present a taxonomic framework and a phylogenetic foundation for all future research on the Micropholcommatidae; a template by which new species can be described and existing species can be identified, and a valuable dataset for exploring phylogenetic hypotheses.

Author: Jimmy Cabra-Garcia
Publisher:
ISBN: 9781775578765
Category : Tetragnathidae
Languages : en
Pages :

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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 centralisChamberlin, 1925 with Glenognatha minuta Banks, 1898.

Author: Karin Schütt
Publisher:
ISBN:
Category : Spiders
Languages : en
Pages : 160

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Author: Elizabeth Danielle Morrill
Publisher:
ISBN:
Category : Desidae
Languages : en
Pages : 292

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Author: Charles E. Griswold
Publisher:
ISBN:
Category : Amaurobiidae
Languages : en
Pages : 214

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"The subfamily Phyxelidinae Lehtinen of the Amaurobiidae is diagnosed and revised, and a key to and distribution maps of the 53 valid and 1 undescribed species are provided. The subfamily comprises 12 genera placed in three newly described tribes: Ambohima, new genus, Kulalania new genus, Lamaika, new genus, Malaika Lehtinen, Matundua Lehtinen, Namaquarachne, new genus, Phyxelida Simon, Pongolania, new genus, Themacrys Simon, Vidole Lehtinen, Vytfutia Deeleman-Reinhold, and Xevioso Lehtinen. Vytfutia is newly transferred to the Phyxelidinae. Members of the Phyxelidinae occur in Africa, Madagascar, the eastern Mediterranean, and southeast Asia. The Phyxelidinae is monophyletic and is defined by the following putative synapomorphies: at least some of the basal prolateral setae on the palpal femora of both sexes are enlarged, and in many species the setae are also modified into thorns; the tarsal trichobothria are lost and the metatarsal pattern is reduced to a single subapical dorsal trichobothrium; and the origin of the calamistrum is shifted to the median part of the fourth metatarsus. Previous familial placements of the spiders here placed in the Phyxelidinae are critically evaluated, and it is concluded that the Phyxelidinae are members of the Amaurobiidae. The Amaurobiidae is redefined on the basis of putative synapomorphies as spiders with a divided cribellum which have simple, sclerotized retrolateral and dorsal tibial processes on the male palp (however, the retrolateral process is lost in all Phyxelidinae except Vytfutia). A cladogram for the 54 species of the Phyxelidinae derived through numerical parsimony analysis using Swofford's program PAUP is presented. The following new taxa are proposed: new tribes: Vytfutiini, Vidoleini, and Phyxelidini; new genera: Ambohima (type species Ambohima sublima, new species, from Madagascar), Kulalania (type species Kulalania antiqua, new species, from Kenya), Lamaika (type species Lamaika distincta, new species, from South Africa), Namaquarachne (type species Namaquarachne khoikhoiana, new species, from South Africa), and Pongolania (type species Pongolania pongola, new species, from South Africa); new species: Ambohima sublima and A. pauliani; Kulalania antiqua; Lamaika distincta; Malaika delicatula; Namaquarachne angulata, N. khoikhoiana, N. thaumatula, and N. tropata; Phyxelida abyssinica, P. anatolica, P. apwania, P. carcharata, P. crassibursa, P. eurygyna, P. fanivelona, P. irwini, P. jabalina, P. kipia, P. malagasyana P. pingoana, P. sindanoa, and P. umlima; Pongolania chrysionaria and P. pongola; Themacrys ukhahlamba; Vidole V. helicigyna, V. lyra, and V. sothoana; Xevioso amica, X. aululata, X. colobata, X. jocquei, X. kulufa, X. lichmadina, and X. orthomeles. The following new synonymies are proposed: Haemilla grindleyi Lawrence with Malaika longipes (Purcell); Haemilla profundissima Lawrence with Vidole capensis (Pocock). The synonymies of Auximus schreineri Purcell with Auximus capensis Pocock, and of Haemilla tanganensis Simon and Fage with Amphigyrum nebulosum Tullgren, are rejected. Themacrys stolida Simon is considered a nomen dubium"--Page 3

Author: Martín J. Ramírez
Publisher:
ISBN:
Category : Amaurobioidinae
Languages : en
Pages : 268

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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 Ramírez, 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 tridentata Simon, including also Axyracrus coccineus Mello-Leitão, Clubiona paduana Karsch, Gayenna excepta Tullgren, Gayenna exigua Mello-Leitão, and Tomopisthes lebruni Simon). The previously revised genera Acanthoceto Mello-Leitão and Ferrieria Tullgren are also included 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 Argentina. Arachosia O.P.-Cambridge comprises many species previously assigned to Oxysoma. Abuzaida striata Keyserling, Anyphaena oblonga Keyserling, Gayenna proseni Mello-Leitão, Gayenna duplovittata Mello-Leitão, Gayenna bonneti Mello-Leitão, Oxysoma dubium Berland, Oxysoma bifasciatum Mello-Leitão, Oxysoma cubana Banks, Oxysoma polytrichium Mello-Leitão, Phidyle bergi Simon, and Samuza praesignis Keyserling are transferred to Arachosia. The males of Arachosia bergi (Simon), A. honesta Keyserling, and Arachosia praesignis (Keyserling) 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 assigned to the genus Sanogasta Mello-Leitão 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-Leitão, Gayenna rufithorax Tullgren, Gayenna x-signata Keyserling, 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 Ramírez and Monapia angusta (Mello-Leitão) 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-Leitão, Gayenna reticulata Mello-Leitão, Gayenna taperae Mello-Leitão, Oxysoma quinquenotatum Simon, Oxysoma unipunctatum Simon, Oxysoma novum Mello-Leitão, Oxysoma lineatum Tullgren, and Tomopisthes frenatus Mello-Leitão are transferred to Tasata. The males of Tasata parcepunctata Simon, T. variolosa Mello-Leitão, 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-Leitão, with Axyracrus Simon; Schiapellia gerschmanni Mello-Leitão and Amaurobioides boydi Forster, with Axyracrus elegans Simon; Tomopisthes magellanicus 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-Leitão, with Arachosia honesta Keyserling; Sanogasta intermedia Mello-Leitão, 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 immanis Simon, Heteromma fuegiana Karsch, Philisca sica Strand, and Nonianus argentinus Mello-Leitão, 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: Raymond R. Forster
Publisher:
ISBN:
Category : Arachnida
Languages : en
Pages : 120

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"The previously monotypic subfamily Physogleninae Petrunkevitch is redefined to include Physoglenes Simon--containing P. vivesi Simon and three new species from Chile--and three new genera: Meringa, containing nine new species from New Zealand; Tupua, containing four new species from Tasmania; and Paratupua, containing one new species from Victoria. The physoglenine genera are united by unique modifications of the male pedicel and anterior abdominal region. The new subfamily Pahorinae is established for five new genera from New Zealand: Pahora (containing nine new species), Pahoroides (containing two new species), Wairua (containing two new species), Nomaua (containing five new species and N. crinifrons (Urquhart), transferred from the linyphiid genus Bolyphantes), and Runga (containing five new species). The pahorine genera are united by a carapace-abdomen stridulatory system, secretory pores on the male pars cephalica, and a deeply excavated paracymbial area on the male palp. Three other genera seem closely related to physoglenines and pahorines: Mangua, new genus, containing 13 new species and M. forsteri (Brignoli), transferred from Linyphia, all from New Zealand; Chileotaxus, new genus, containing one new species from Chile; and the Neotropical genus Synotaxus Simon. These spiders have been widely separated in some past classifications; Physoglenes has been variously considered a leptonetid, pholcid, theridiid, or araneoid incertae sedis, whereas the other previously described taxa have generally been considered theridiids or linyphiids. All 12 genera are united by the presence of a small, basally situated and dorsally excavated paracymbium, a longitudinal incision of the retrolateral cymbial margin, thickened (and sometimes spiniform) dorsal macrosetae on the male palpal femur, patella, and/or tibia, and greatly elongated, spineless legs, with the first pair much the longest and all femora basally thickened. The known web forms are diverse, including an irregular sheet (Mangua and at least some physoglenines), an inverted bowl (pahorines), and a latticelike structure (Synotaxus). The absence of a comb on tarsi IV and widened aggregate spigots on the posterior lateral spinnerets, and the presence of a basal paracymbium, indicate that these genera do not belong to the Theridiidae, and the male palpi lack the distinct embolic division including a radix typical of the Linyphiidae. The oldest family-group name available for the assemblage is Synotaxidae, based on Synotaxeae Simon. Synotaxidae is hypothesized to be the sister group of Nesticidae plus Theridiidae. Wunderlich's synonymy of the families Hadrotarsidae and Theridiidae appears to be justified by paracymbial morphology; two possibly monophyletic groups can be recognized among the genera that are currently considered valid members of those families. The genera Anatea Berland, Audifia Keyserling, Dipoena Thorell, Dipoenata Wunderlich, Euryopis Menge, Gmogola Keyserling, Guaraniella Baert, Hadrotarsus Thorell, Lasaeola Simon, and Yoroa Baert are apparently united by a suite of characters (a dorsoventrally flattened female palpal claw, shortened chelicerae with elongated fangs, specialized ventral setae on tarsus I, a series of parallel ridges on the medial surface of the anterior lateral spinnerets, and four rather than two spermathecae) and may all be specialized predators of ants; the earliest available name for the assemblage is Hadrotarsinae Thorell. At least the genera Anelosimus Simon, Chrosiothes Simon, Chrysso O.P.-Cambridge, Coleosoma O.P.-Cambridge, Helvibis Keyserling, Nesticodes Archer, Rugathodes Archer, Spintharus Hentz, Tekellina Levi, Theridula Emerton, Thwaitesia O.P.-Cambridge, and Thymoites Keyserling are apparently united by a distinctive paracymbial hood. The name Spintharinae Simon is available for this assemblage; if Spintharinae is monophyletic, the genera Achaearanea Strand and Anelosimus, as currently construed, may be polyphyletic assemblages that require relimitation"--Page 3