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The First Record of Family Segestriidae Simon, 1893 (Araneae: Dysderoidea) from Iran
Serket (2014) vol. 14(1): 15-18. The first record of family Segestriidae Simon, 1893 (Araneae: Dysderoidea) from Iran Alireza Zamani Department of Animal Biology, School of Biology and Center of Excellence in Phylogeny of Living Organisms in Iran, College of Science, University of Tehran, Tehran, Iran [email protected] Abstract The family Segestriidae Simon, 1893 and the species Segestria senoculata (Linnaeus, 1758) are recorded in Iran for the first time, based on a single female specimen. Keywords: Spiders, Segestriidae, Segestria senoculata, new record, Iran. Introduction Segestriidae Simon, 1893 is a small family of medium-sized, araneomorph, ecribellate, haplogyne spiders with three tarsal claws which are globally represented by 119 species in three genera (Platnick, 2014). These spiders are six-eyed, and are usually distinguishable by having their third pair of legs directed forwards. From taxonomic point of view, Segestriidae is closely related to Dysderidae, and are considered as a member of the superfamily Dysderoidea. The type genus, Segestria Latreille, 1804, is consisted of 18 species and one subspecies which are mostly distributed in the Palaearctic ecozone (Platnick, 2014). One of the more distributed species is Segestria senoculata (Linnaeus, 1758). This species, like most segestriids, occupies a wide variety of habitats; they prefer living in holes within walls and barks, or under stones, where they build a tubular retreat, with strong threads of silk radiating from the entrance (Roberts, 1995). So far, about 500 spider species of more than 38 families have been reported from Iran (based on our upcoming work on the renewed checklist and the history of studies), but no documentation of the family Segestriidae has been reported from Iran (Mozaffarian & Marusik, 2001; Ghavami, 2006; Kashefi et al., 2013). -
Arachnida: Araneae) Para México Y Listado Actualizado De La Araneofauna Del Estado De Coahuila
ISSN 0065-1737 (NUEVA SERIE) 34(1) 2018 e ISSN 2448-8445 NUEVOS REGISTROS DE ARAÑAS (ARACHNIDA: ARANEAE) PARA MÉXICO Y LISTADO ACTUALIZADO DE LA ARANEOFAUNA DEL ESTADO DE COAHUILA NEW RECORDS OF SPIDERS (ARACHNIDA: ARANEAE) FROM MEXICO AND LISTING OF SPIDERS FROM COAHUILA STATE Marco Antonio DESALES-LARA,1,2 María Luisa JIMÉNEZ3,* y Pablo CORCUERA2 1 Doctorado en Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana-Iztapalapa (UAM-I). Av. San Rafael Atlixco 186. Col. Vicentina Iztapalapa, C.P. 09340, Cd de México, México <[email protected]> 2 Laboratorio de Ecología Animal, Departamento de Biología, Universidad Autónoma Metropolitana-Iztapalapa (UAM-I). Av. San Rafael Atlixco 186. Col. Vicentina Iztapalapa, C.P. 09340, Cd de México, México. <pcmr@ xanum.uam.mx> 3 Laboratorio de Aracnología y Entomología, Centro de Investigaciones Biológicas del Noroeste. Instituto Politécnico Nacional 195, Col. Playa Palo de Santa Rita Sur, C.P. 23096 La Paz, Baja California Sur, México. <[email protected]> *Autor para correspondencia: <[email protected]> Recibido: 27/06/2017; aceptado: 01/12/2017 Editor responsable: Guillermo Ibarra Núñez Desales-Lara, M. A., Jiménez, M. L. y Corcuera, P. (2018) Nuevos Desales-Lara, M. A., Jiménez, M. L., & Corcuera, P. (2018) New registros de arañas (Arachnida: Araneae) para México y listado records of spiders (Arachnida: Araneae) from Mexico and listing actualizado de la araneofauna del estado de Coahuila. Acta Zooló- of spiders from Coahuila state. Acta Zoológica Mexicana (n.s), gica Mexicana (n.s), 34(1), 50-63. 34(1), 50-63. RESUMEN. Se dan a conocer cuatro nuevos registros de especies ABSTRACT. -
Comparative Functional Morphology of Attachment Devices in Arachnida
Comparative functional morphology of attachment devices in Arachnida Vergleichende Funktionsmorphologie der Haftstrukturen bei Spinnentieren (Arthropoda: Arachnida) DISSERTATION zur Erlangung des akademischen Grades doctor rerum naturalium (Dr. rer. nat.) an der Mathematisch-Naturwissenschaftlichen Fakultät der Christian-Albrechts-Universität zu Kiel vorgelegt von Jonas Otto Wolff geboren am 20. September 1986 in Bergen auf Rügen Kiel, den 2. Juni 2015 Erster Gutachter: Prof. Stanislav N. Gorb _ Zweiter Gutachter: Dr. Dirk Brandis _ Tag der mündlichen Prüfung: 17. Juli 2015 _ Zum Druck genehmigt: 17. Juli 2015 _ gez. Prof. Dr. Wolfgang J. Duschl, Dekan Acknowledgements I owe Prof. Stanislav Gorb a great debt of gratitude. He taught me all skills to get a researcher and gave me all freedom to follow my ideas. I am very thankful for the opportunity to work in an active, fruitful and friendly research environment, with an interdisciplinary team and excellent laboratory equipment. I like to express my gratitude to Esther Appel, Joachim Oesert and Dr. Jan Michels for their kind and enthusiastic support on microscopy techniques. I thank Dr. Thomas Kleinteich and Dr. Jana Willkommen for their guidance on the µCt. For the fruitful discussions and numerous information on physical questions I like to thank Dr. Lars Heepe. I thank Dr. Clemens Schaber for his collaboration and great ideas on how to measure the adhesive forces of the tiny glue droplets of harvestmen. I thank Angela Veenendaal and Bettina Sattler for their kind help on administration issues. Especially I thank my students Ingo Grawe, Fabienne Frost, Marina Wirth and André Karstedt for their commitment and input of ideas. -
The Common Spiders of Antelope Island State Park
THE COMMON SPIDERS OF ANTELOPE ISLAND STATE PARK by Stephanie M Cobbold Web-building Spiders ______________________________________________________________________________ Family Araneidae (orb web spiders) Build a circular spiral web on support lines that radiate out from the center The spider is often found waiting for prey in the center of its web Typical eye pattern: 4 median eyes clustered in a square shape Eye pattern Orb web SMC SMC Neoscona (back and front views) Banded Garden Spider (Argiope) 1 ______________________________________________________________________________ Family Theridiidae (cob web spiders) Abdomen usually ball or globe-shaped Have bristles on legs called combs. These combs are used to fling silk strands over captive prey. Web is loose, irregular and 3-dimensional commons.wikimedia.org Black Widow (Latrodectus hesperus) Theridion ________________________________________________________________________ Family Linyphiidae (sheet web spiders) Build flat, sheet-like or dome-shaped webs under which the spider hangs upside- down. Abdomen is usually longer than wide SMC Sheet web spider hanging under its web 2 ________________________________________________________________________ Family Dictynidae (mesh web spiders) Make small, irregular webs of hackled threads Often found near the tips of plants SMC ________________________________________________________________________ Family Agelenidae (funnel web spiders) Web is a silk mat with a funnel-shaped retreat at one end in which the spider waits in ambush -
Arachnids (Excluding Acarina and Pseudoscorpionida) of the Wichita Mountains Wildlife Refuge, Oklahoma
OCCASIONAL PAPERS THE MUSEUM TEXAS TECH UNIVERSITY NUMBER 67 5 SEPTEMBER 1980 ARACHNIDS (EXCLUDING ACARINA AND PSEUDOSCORPIONIDA) OF THE WICHITA MOUNTAINS WILDLIFE REFUGE, OKLAHOMA JAMES C. COKENDOLPHER AND FRANK D. BRYCE The Wichita Mountains are located in eastern Greer, southern Kiowa, and northwestern Comanche counties in Oklahoma. Since their formation more than 300 million years ago, these rugged mountains have been fragmented and weathered, until today the highest peak (Mount Pinchot) stands only 756 meters above sea level (Tyler, 1977). The mountains are composed predominantly of granite and gabbro. Forests of oak, elm, and walnut border most waterways, while at elevations from 153 to 427 meters prair ies are the predominant vegetation type. A more detailed sum mary of the climatic and biotic features of the Wichitas has been presented by Blair and Hubbell (1938). A large tract of land in the eastern range of the Wichita Moun tains (now northeastern Comanche County) was set aside as the Wichita National Forest by President McKinley during 1901. In 1905, President Theodore Roosevelt created a game preserve on those lands managed by the Forest Service. Since 1935, this pre serve has been known as the Wichita Mountains Wildlife Refuge. Numerous papers on Oklahoma spiders have been published (Bailey and Chada, 1968; Bailey et al., 1968; Banks et al, 1932; Branson, 1958, 1959, 1966, 1968; Branson and Drew, 1972; Gro- thaus, 1968; Harrel, 1962, 1965; Horner, 1975; Rogers and Horner, 1977), but only a single, comprehensive work (Banks et al., 1932) exists covering all arachnid orders in the state. Further additions and annotations to the arachnid fauna of Oklahoma can be found 2 OCCASIONAL PAPERS MUSEUM TEXAS TECH UNIVERSITY in recent revisionary studies. -
Sexual Selection Research on Spiders: Progress and Biases
Biol. Rev. (2005), 80, pp. 363–385. f Cambridge Philosophical Society 363 doi:10.1017/S1464793104006700 Printed in the United Kingdom Sexual selection research on spiders: progress and biases Bernhard A. Huber* Zoological Research Institute and Museum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany (Received 7 June 2004; revised 25 November 2004; accepted 29 November 2004) ABSTRACT The renaissance of interest in sexual selection during the last decades has fuelled an extraordinary increase of scientific papers on the subject in spiders. Research has focused both on the process of sexual selection itself, for example on the signals and various modalities involved, and on the patterns, that is the outcome of mate choice and competition depending on certain parameters. Sexual selection has most clearly been demonstrated in cases involving visual and acoustical signals but most spiders are myopic and mute, relying rather on vibrations, chemical and tactile stimuli. This review argues that research has been biased towards modalities that are relatively easily accessible to the human observer. Circumstantial and comparative evidence indicates that sexual selection working via substrate-borne vibrations and tactile as well as chemical stimuli may be common and widespread in spiders. Pattern-oriented research has focused on several phenomena for which spiders offer excellent model objects, like sexual size dimorphism, nuptial feeding, sexual cannibalism, and sperm competition. The accumulating evidence argues for a highly complex set of explanations for seemingly uniform patterns like size dimorphism and sexual cannibalism. Sexual selection appears involved as well as natural selection and mechanisms that are adaptive in other contexts only. Sperm competition has resulted in a plethora of morpho- logical and behavioural adaptations, and simplistic models like those linking reproductive morphology with behaviour and sperm priority patterns in a straightforward way are being replaced by complex models involving an array of parameters. -
Spiders of the Hawaiian Islands: Catalog and Bibliography1
Pacific Insects 6 (4) : 665-687 December 30, 1964 SPIDERS OF THE HAWAIIAN ISLANDS: CATALOG AND BIBLIOGRAPHY1 By Theodore W. Suman BISHOP MUSEUM, HONOLULU, HAWAII Abstract: This paper contains a systematic list of species, and the literature references, of the spiders occurring in the Hawaiian Islands. The species total 149 of which 17 are record ed here for the first time. This paper lists the records and literature of the spiders in the Hawaiian Islands. The islands included are Kure, Midway, Laysan, French Frigate Shoal, Kauai, Oahu, Molokai, Lanai, Maui and Hawaii. The only major work dealing with the spiders in the Hawaiian Is. was published 60 years ago in " Fauna Hawaiiensis " by Simon (1900 & 1904). All of the endemic spiders known today, except Pseudanapis aloha Forster, are described in that work which also in cludes a listing of several introduced species. The spider collection available to Simon re presented only a small part of the entire Hawaiian fauna. In all probability, the endemic species are only partly known. Since the appearance of Simon's work, there have been many new records and lists of introduced spiders. The known Hawaiian spider fauna now totals 149 species and 4 subspecies belonging to 21 families and 66 genera. Of this total, 82 species (5596) are believed to be endemic and belong to 10 families and 27 genera including 7 endemic genera. The introduced spe cies total 65 (44^). Two unidentified species placed in indigenous genera comprise the remaining \%. Seventeen species are recorded here for the first time. In the catalog section of this paper, families, genera and species are listed alphabetical ly for convenience. -
The Placement of the Spider Genus Periegops and the Phylogeny of Scytodoidea (Araneae: Araneomorphae)
Zootaxa 3312: 1–44 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) The placement of the spider genus Periegops and the phylogeny of Scytodoidea (Araneae: Araneomorphae) FACUNDO M. LABARQUE1 & MARTÍN J. RAMÍREZ1 1Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Ángel Gallardo 470, C1405DJR, Buenos Aires, Argentina. [email protected] / [email protected] Abstract The relationships of Scytodoidea, including the families Drymusidae, Periegopidae, Scytodidae and Sicariidae, have been con- tentious for a long time. Here we present a reviewed phylogenetic analysis of scytodoid spiders, emphasizing Periegops, the only genus in the family Periegopidae. In our analysis the Scytodoidea are united by the fusion of the third abdominal entapo- physes into a median lobe, the presence of female palpal femoral thorns and associated cheliceral stridulatory ridges, a mem- branous lobe on the cheliceral promargin, and the loss of minor ampullate gland spigots. A basal split within Scytodoidea defines two monophyletic groups: Sicariidae and a group formed by Scytodidae as the sister group of Periegopidae plus Dry- musidae, all united by having bipectinate prolateral claws on tarsi I–II, one major ampullate spigot accompanied by a nubbin, and the posterior median spinnerets with a mesal field of spicules. Periegops is the sister group of Drymusidae, united by the regain of promarginal cheliceral teeth and a triangular cheliceral lamina, which is continuous with the paturon margin. Key words: Drymusa, Drymusidae, Haplogyne, morphology, Scytodes, Stedocys, Scytodidae, Sicariidae, Sicarius, Loxosceles Introduction The family Periegopidae currently comprises only the genus Periegops, with two species: the type species Perie- gops suteri (Urquhart) from the Banks Peninsula on the South Island of New Zealand (Vink 2006), and Periegops australia Forster, from southeastern Queensland (Forster 1995). -
A Protocol for Online Documentation of Spider Biodiversity Inventories Applied to a Mexican Tropical Wet Forest (Araneae, Araneomorphae)
Zootaxa 4722 (3): 241–269 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2020 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4722.3.2 http://zoobank.org/urn:lsid:zoobank.org:pub:6AC6E70B-6E6A-4D46-9C8A-2260B929E471 A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae) FERNANDO ÁLVAREZ-PADILLA1, 2, M. ANTONIO GALÁN-SÁNCHEZ1 & F. JAVIER SALGUEIRO- SEPÚLVEDA1 1Laboratorio de Aracnología, Facultad de Ciencias, Departamento de Biología Comparada, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Colonia Copilco el Bajo. C. P. 04510. Del. Coyoacán, Ciudad de México, México. E-mail: [email protected] 2Corresponding author Abstract Spider community inventories have relatively well-established standardized collecting protocols. Such protocols set rules for the orderly acquisition of samples to estimate community parameters and to establish comparisons between areas. These methods have been tested worldwide, providing useful data for inventory planning and optimal sampling allocation efforts. The taxonomic counterpart of biodiversity inventories has received considerably less attention. Species lists and their relative abundances are the only link between the community parameters resulting from a biotic inventory and the biology of the species that live there. However, this connection is lost or speculative at best for species only partially identified (e. g., to genus but not to species). This link is particularly important for diverse tropical regions were many taxa are undescribed or little known such as spiders. One approach to this problem has been the development of biodiversity inventory websites that document the morphology of the species with digital images organized as standard views. -
A Summary List of Fossil Spiders
A summary list of fossil spiders compiled by Jason A. Dunlop (Berlin), David Penney (Manchester) & Denise Jekel (Berlin) Suggested citation: Dunlop, J. A., Penney, D. & Jekel, D. 2010. A summary list of fossil spiders. In Platnick, N. I. (ed.) The world spider catalog, version 10.5. American Museum of Natural History, online at http://research.amnh.org/entomology/spiders/catalog/index.html Last udated: 10.12.2009 INTRODUCTION Fossil spiders have not been fully cataloged since Bonnet’s Bibliographia Araneorum and are not included in the current Catalog. Since Bonnet’s time there has been considerable progress in our understanding of the spider fossil record and numerous new taxa have been described. As part of a larger project to catalog the diversity of fossil arachnids and their relatives, our aim here is to offer a summary list of the known fossil spiders in their current systematic position; as a first step towards the eventual goal of combining fossil and Recent data within a single arachnological resource. To integrate our data as smoothly as possible with standards used for living spiders, our list follows the names and sequence of families adopted in the Catalog. For this reason some of the family groupings proposed in Wunderlich’s (2004, 2008) monographs of amber and copal spiders are not reflected here, and we encourage the reader to consult these studies for details and alternative opinions. Extinct families have been inserted in the position which we hope best reflects their probable affinities. Genus and species names were compiled from established lists and cross-referenced against the primary literature. -
Alexander Sánchez-Ruiz
ARTÍCULO: CURRENT TAXONOMIC STATUS OF THE FAMILY CAPONIIDAE (ARACHNIDA, ARANEAE) IN CUBA WITH THE DESCRIPTION OF TWO NEW SPECIES Alexander Sánchez-Ruiz Abstract: All information known about the spider species of the family Caponiidae recorded from Cuba is compiled. Two new species of the genus Nops MacLeay, 1839 (Araneae, Caponiidae) are described from eastern Cuba, raising to seven the number of species in the Caponiidae fauna of this archipelago. Key words: Araneae, Caponiidae, taxonomy, West Indies, Cuba. Taxonomy: Nops enae sp. n. Nops siboney sp. n. ARTÍCULO: Current taxonomic status of the Estado taxonómico actual de la familia Caponiidae (Arachnida, Araneae) en family Caponiidae (Arachnida, Cuba y descripción de dos especies nuevas Araneae) in Cuba with the description of two new species Resumen: Se recopila toda la información conocida acerca de las especies de arañas de la familia Alexander Sánchez-Ruiz Caponiidae registradas para Cuba. Se describen dos nuevas especies del género Nops Centro Oriental de Ecosistemas y MacLeay, 1839 (Araneae, Caponiidae) procedentes del oriente de Cuba, alcanzando las Biodiversidad, Museo de Historia siete especies la fauna de Caponiidae de este archipiélago. Natural “Tomás Romay”, José A. Palabras clave: Araneae, Caponiidae, taxonomía, Antillas, Cuba. Saco # 601, Santiago de Cuba Taxonomía: 90100, Cuba. Nops enae sp. n. [email protected] Nops siboney sp. n. Revista Ibérica de Aracnología ISSN: 1576 - 9518. Dep. Legal: Z-2656-2000. Introduction Vol. 9, 30-VI-2004 Sección: Artículos y Notas. The family Caponiidae in the New World is represented by nine genera: Calponia Pp: 95–102. Platnick 1993, Caponina Simon, 1891, Nops MacLeay, 1839, Nopsides Chamberlin, 1924, Notnops Platnick, 1994, Orthonops Chamberlin, 1924, Taintnops Platnick, Edita: 1994, Tarsonops Chamberlin, 1924 and Tisentnops Platnick, 1994. -
140063122.Pdf
Dtet specia|isatlon and ďverslÍlcatlon oftlrc sf,der genrs Dysdara (Araneae: Dysdertdae) Summaryof PhD. thesis Tho main aim of my sfudy is to pr€s€nt now knowledge about the diet specialisation antl diversiÍicationóf ttre ipider genusDys&ra. This PhD. lhesis, ďvided in two parts' is tre summary of Íive papers. 1. Diet specialisatlon 1.1. Řezíě M., Pekór s. & I'bin Y.: Morphologlcal and behavlourď adapations for onlscophagr lnDysderassden (Araneae: Dysdertnne) [acoeptedby Journal of Zoologfl Very little is known about predators feeding on woodlioe. Spiders of the genus Dyidera (Dysderidae) were long suspeotedto be onisoophagous,but evidenoe for lheir díet speoialisation hás beenrlaoking. These spidas are chareotorised by an unusual morphological variability oftheir mouth-parts,partioularly tho ohelioaae, suggosting dietary sfrcialisation któróukazuje na potavní specializaci. Thus, we investigatedthe rebtiónsirip between mouthpertmorphology, prey pÍeferenoeand predatory belraviour of ťrvespecies represerrtingdiffoent chelioenď types. Resulb obtained sugg€st that sfudiedĎysdera spidas diffo in prey specialisetion for woďlioo. The species with unmodified chelicerae reatlity oapturedvarious artkopďs but refused woodlice while speoieswith modified ohetóerae oapfuredwoodlice' Particularly,Dysdera erythrina ind D. spinrcrus captured woodlioe as freque,lrtý as ďternativo pfey typ€s. Dysdera abdomiialis andD. dubrovnlnrii sigrificantly preforred woodlice to alternative prey. Cheliooď modifioations were found to detormine the grasping bohaviour. Species 'pinoers with elongated chelicerae used a taotio" i.e. insertd one chelicera into the soft ventil side and plaoed lhe olher on the dorsal side of woodlouse. Species with .fork dorsally ooncave chálicerae used a tactio': they fuckod thom quiokly under woodlóuse in order to bite the vental side of woodlouse body. Specios with flattonď .key chelicerae usď a tactic': lhey inserted a flattraredchelicera betweon sclerites of the armouredwoodlouse.