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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. -
The Phylogenetic Distribution of Sphingomyelinase D Activity in Venoms of Haplogyne Spiders
Comparative Biochemistry and Physiology Part B 135 (2003) 25–33 The phylogenetic distribution of sphingomyelinase D activity in venoms of Haplogyne spiders Greta J. Binford*, Michael A. Wells Department of Biochemistry and Molecular Biophysics, University of Arizona, Tucson, AZ 85721, USA Received 6 October 2002; received in revised form 8 February 2003; accepted 10 February 2003 Abstract The venoms of Loxosceles spiders cause severe dermonecrotic lesions in human tissues. The venom component sphingomyelinase D (SMD) is a contributor to lesion formation and is unknown elsewhere in the animal kingdom. This study reports comparative analyses of SMD activity and venom composition of select Loxosceles species and representatives of closely related Haplogyne genera. The goal was to identify the phylogenetic group of spiders with SMD and infer the timing of evolutionary origin of this toxin. We also preliminarily characterized variation in molecular masses of venom components in the size range of SMD. SMD activity was detected in all (10) Loxosceles species sampled and two species representing their sister taxon, Sicarius, but not in any other venoms or tissues surveyed. Mass spectrometry analyses indicated that all Loxosceles and Sicarius species surveyed had multiple (at least four to six) molecules in the size range corresponding to known SMD proteins (31–35 kDa), whereas other Haplogynes analyzed had no molecules in this mass range in their venom. This suggests SMD originated in the ancestors of the Loxoscelesy Sicarius lineage. These groups of proteins varied in molecular mass across species with North American Loxosceles having 31–32 kDa, African Loxosceles having 32–33.5 kDa and Sicarius having 32–33 kDa molecules. -
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). -
Anza-Borrego Desert State Park Bibliography Compiled and Edited by Jim Dice
Steele/Burnand Anza-Borrego Desert Research Center University of California, Irvine UCI – NATURE and UC Natural Reserve System California State Parks – Colorado Desert District Anza-Borrego Desert State Park & Anza-Borrego Foundation Anza-Borrego Desert State Park Bibliography Compiled and Edited by Jim Dice (revised 1/31/2019) A gaggle of geneticists in Borrego Palm Canyon – 1975. (L-R, Dr. Theodosius Dobzhansky, Dr. Steve Bryant, Dr. Richard Lewontin, Dr. Steve Jones, Dr. TimEDITOR’S Prout. Photo NOTE by Dr. John Moore, courtesy of Steve Jones) Editor’s Note The publications cited in this volume specifically mention and/or discuss Anza-Borrego Desert State Park, locations and/or features known to occur within the present-day boundaries of Anza-Borrego Desert State Park, biological, geological, paleontological or anthropological specimens collected from localities within the present-day boundaries of Anza-Borrego Desert State Park, or events that have occurred within those same boundaries. This compendium is not now, nor will it ever be complete (barring, of course, the end of the Earth or the Park). Many, many people have helped to corral the references contained herein (see below). Any errors of omission and comission are the fault of the editor – who would be grateful to have such errors and omissions pointed out! [[email protected]] ACKNOWLEDGEMENTS As mentioned above, many many people have contributed to building this database of knowledge about Anza-Borrego Desert State Park. A quantum leap was taken somewhere in 2016-17 when Kevin Browne introduced me to Google Scholar – and we were off to the races. Elaine Tulving deserves a special mention for her assistance in dealing with formatting issues, keeping printers working, filing hard copies, ignoring occasional foul language – occasionally falling prey to it herself, and occasionally livening things up with an exclamation of “oh come on now, you just made that word up!” Bob Theriault assisted in many ways and now has a lifetime job, if he wants it, entering these references into Zotero. -
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. -
First Insights Into the Subterranean Crustacean Bathynellacea
RESEARCH ARTICLE First Insights into the Subterranean Crustacean Bathynellacea Transcriptome: Transcriptionally Reduced Opsin Repertoire and Evidence of Conserved Homeostasis Regulatory Mechanisms Bo-Mi Kim1, Seunghyun Kang1, Do-Hwan Ahn1, Jin-Hyoung Kim1, Inhye Ahn1,2, Chi- Woo Lee3, Joo-Lae Cho4, Gi-Sik Min3*, Hyun Park1,2* a1111111111 1 Unit of Polar Genomics, Korea Polar Research Institute, Incheon, South Korea, 2 Polar Sciences, a1111111111 University of Science & Technology, Yuseong-gu, Daejeon, South Korea, 3 Department of Biological a1111111111 Sciences, Inha University, Incheon, South Korea, 4 Nakdonggang National Institute of Biological Resources, a1111111111 Sangju, South Korea a1111111111 * [email protected] (HP); [email protected] (GM) Abstract OPEN ACCESS Bathynellacea (Crustacea, Syncarida, Parabathynellidae) are subterranean aquatic crusta- Citation: Kim B-M, Kang S, Ahn D-H, Kim J-H, Ahn I, Lee C-W, et al. (2017) First Insights into the ceans that typically inhabit freshwater interstitial spaces (e.g., groundwater) and are occa- Subterranean Crustacean Bathynellacea sionally found in caves and even hot springs. In this study, we sequenced the whole Transcriptome: Transcriptionally Reduced Opsin transcriptome of Allobathynella bangokensis using RNA-seq. De novo sequence assembly Repertoire and Evidence of Conserved produced 74,866 contigs including 28,934 BLAST hits. Overall, the gene sequences were Homeostasis Regulatory Mechanisms. PLoS ONE 12(1): e0170424. doi:10.1371/journal. most similar to those of the waterflea Daphnia pulex. In the A. bangokensis transcriptome, pone.0170424 no opsin or related sequences were identified, and no contig aligned to the crustacean visual Editor: Peng Xu, Xiamen University, CHINA opsins and non-visual opsins (i.e. -
Tarantulas and Social Spiders
Tarantulas and Social Spiders: A Tale of Sex and Silk by Jonathan Bull BSc (Hons) MSc ICL Thesis Presented to the Institute of Biology of The University of Nottingham in Partial Fulfilment of the Requirements for the Degree of Doctor of Philosophy The University of Nottingham May 2012 DEDICATION To my parents… …because they both said to dedicate it to the other… I dedicate it to both ii ACKNOWLEDGEMENTS First and foremost I would like to thank my supervisor Dr Sara Goodacre for her guidance and support. I am also hugely endebted to Dr Keith Spriggs who became my mentor in the field of RNA and without whom my understanding of the field would have been but a fraction of what it is now. Particular thanks go to Professor John Brookfield, an expert in the field of biological statistics and data retrieval. Likewise with Dr Susan Liddell for her proteomics assistance, a truly remarkable individual on par with Professor Brookfield in being able to simplify even the most complex techniques and analyses. Finally, I would really like to thank Janet Beccaloni for her time and resources at the Natural History Museum, London, permitting me access to the collections therein; ten years on and still a delight. Finally, amongst the greats, Alexander ‘Sasha’ Kondrashov… a true inspiration. I would also like to express my gratitude to those who, although may not have directly contributed, should not be forgotten due to their continued assistance and considerate nature: Dr Chris Wade (five straight hours of help was not uncommon!), Sue Buxton (direct to my bench creepy crawlies), Sheila Keeble (ventures and cleans where others dare not), Alice Young (read/checked my thesis and overcame her arachnophobia!) and all those in the Centre for Biomolecular Sciences. -
A List of Utah Spiders, with Their Localities
Great Basin Naturalist Volume 43 Number 3 Article 22 7-31-1983 A list of Utah spiders, with their localities Dorald M. Allred Brigham Young University B. J. Kaston San Diego State University, San Diego, California Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Allred, Dorald M. and Kaston, B. J. (1983) "A list of Utah spiders, with their localities," Great Basin Naturalist: Vol. 43 : No. 3 , Article 22. Available at: https://scholarsarchive.byu.edu/gbn/vol43/iss3/22 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. A LIST OF UTAH SPIDERS, WITH THEIR LOCALITIES Allred' B. Kaston- Dorald M. and J. Abstract. — The 621 species of spiders known to occnr in Utah as recorded in the Hterature or Utah universities' collections are listed with their junior synonyms and collection localities. Two-fifths (265 species) are known from onlv one locality each, and only one-fifth (123 species) from five or more localities in the state. Little is known of the distribution or eco- Much of our knowledge of Utah spiders logical relationships of Utah spiders. Each of was contributed by Ralph Chamberlin, who 265 species of the 621 recorded for the State authored or coauthored the naming of 220 of is known from only one locality. Even the the species listed for Utah. -
Araneae (Spider) Photos
Araneae (Spider) Photos Araneae (Spiders) About Information on: Spider Photos of Links to WWW Spiders Spiders of North America Relationships Spider Groups Spider Resources -- An Identification Manual About Spiders As in the other arachnid orders, appendage specialization is very important in the evolution of spiders. In spiders the five pairs of appendages of the prosoma (one of the two main body sections) that follow the chelicerae are the pedipalps followed by four pairs of walking legs. The pedipalps are modified to serve as mating organs by mature male spiders. These modifications are often very complicated and differences in their structure are important characteristics used by araneologists in the classification of spiders. Pedipalps in female spiders are structurally much simpler and are used for sensing, manipulating food and sometimes in locomotion. It is relatively easy to tell mature or nearly mature males from female spiders (at least in most groups) by looking at the pedipalps -- in females they look like functional but small legs while in males the ends tend to be enlarged, often greatly so. In young spiders these differences are not evident. There are also appendages on the opisthosoma (the rear body section, the one with no walking legs) the best known being the spinnerets. In the first spiders there were four pairs of spinnerets. Living spiders may have four e.g., (liphistiomorph spiders) or three pairs (e.g., mygalomorph and ecribellate araneomorphs) or three paris of spinnerets and a silk spinning plate called a cribellum (the earliest and many extant araneomorph spiders). Spinnerets' history as appendages is suggested in part by their being projections away from the opisthosoma and the fact that they may retain muscles for movement Much of the success of spiders traces directly to their extensive use of silk and poison. -
4/Ke'icanjluseum PUBLISHED by the AMERICAN MUSEUM of NATURAL HISTORY CENTRAL PARK WEST at 79TH STREET, NEW YORK 24, N.Y
1ovitates4/ke'icanJluseum PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK 24, N.Y. NUMBER 1904 AUGUST 13, 1958 The Spider Fanmily Diguetidae BY WILLIS J. GERTSCH' The primitive six-eyed weavers of the spider family Diguetidae range from the southwestern United States deep into southern Mexico. They have as their nearest relatives the eight-eyed Plectreuridae, which have a similar distribution and are also exclusively American. The elongate, long-legged diguetids weave expansive webs consisting of a maze of threads and move through these webs much in the fashion of aerial spiders. Favorite sites for the webs are the prickly pear and bush cacti of arid regions, but they may be found on almost any kind of shrub vegetation. At the center of the web is suspended vertically a tubular retreat, sometimes fully 3 inches long, which is closed at the top. The females incorporate their egg sacs in the tube, laying one upon the other like the tiles of a roof. The tubes are covered with leaves or plant debris available from the plant supporting the web or from the soil nearby. The family Diguetidae was established by me in 1949 when it was briefly characterized in my book "American spiders" and was listed as a family under the section Plectreuroidea. Until that time it was placed as the subfamily Diguetinae of the family Sicariidae, or Scytodidae. The heterogeneous family Sicariidae of Simon, which was quite valid and suitably proportionate in the terms of his system and conservative fam- ily outlook, was held together largely by a single character. -
The Spiders and Scorpions of the Santa Catalina Mountain Area, Arizona
The spiders and scorpions of the Santa Catalina Mountain Area, Arizona Item Type text; Thesis-Reproduction (electronic) Authors Beatty, Joseph Albert, 1931- Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 29/09/2021 16:48:28 Link to Item http://hdl.handle.net/10150/551513 THE SPIDERS AND SCORPIONS OF THE SANTA CATALINA MOUNTAIN AREA, ARIZONA by Joseph A. Beatty < • • : r . ' ; : ■ v • 1 ■ - ' A Thesis Submitted to the Faculty of the DEPARTMENT OF ZOOLOGY In Partial Fulfillment of the Requirements For the Degree of MASTER OF SCIENCE In the Graduate College UNIVERSITY OF ARIZONA 1961 STATEMENT BY AUTHOR This thesis has been submitted in partial fulfill ment of requirements for an advanced degree at the Uni versity of Arizona and is deposited in the University Library to be made available to borrowers under rules of the Library. Brief quotations from this thesis are allowable without special permission, provided that accurate acknowledgement of source is made. Requests for per mission for extended quotation from or reproduction of this manuscript in whole or in part may be granted by the head of the major department or the Dean of the Graduate College when in their judgment the proposed use of the material is in the interests of scholarship. In all other instances, however, permission must be obtained from the author. -
Odonate Exuviae Used for Roosts and Nests by Sassacus Vitis and Other Jumping Spiders (Araneae: Salticidae)
Peckhamia 142.1 Odonate exuviae used by jumping spiders 1 PECKHAMIA 142.1, 3 June 2016, 1―17 ISSN 2161―8526 (print) ISSN 1944―8120 (online) Odonate exuviae used for roosts and nests by Sassacus vitis and other jumping spiders (Araneae: Salticidae) Tim Manolis 1 1 808 El Encino Way, Sacramento, CA 95864, USA, email: [email protected] Abstract: I systematically collected dragonfly (Anisoptera) exuviae along the margins of backwater lagoons in the American River floodplain, Sacramento County, California, USA, in five years (2008-2010, 2012-13) to document and monitor secondary use of these structures by arthropods, particularly spiders. Of nearly 400 exuviae examined, 28.1% were occupied, or showed signs of occupancy (e.g., unoccupied retreats). Of these occupied exuviae, 93% contained spiders or evidence of spider occupancy, and at least 50% of these were occupied by Sassacus vitis (many unoccupied retreats were probably of that species as well). S. vitis showed a significant preference for using the exuviae of sedentary, burrowing dragonfly larvae versus those of active, clasping or sprawling larvae. I found S. vitis in exuviae as single males and females, in pairs, and using exuviae for molt retreats and nests. Thirty-four S. vitis nests in exuviae provided data on aspects of the species’ breeding biology. In addition, a number of these nests were attacked by hymenopteran egg parasitoids in the genera Idris (Platygastridae) and Gelis (Ichneumonidae). I also found three other salticid species (Sitticus palustris, Synageles occidentalis, and Peckhamia sp.) in exuviae, all guarding egg sacs. Utilization of dragonfly exuviae by Sassacus vitis and other salticids is no doubt more frequent and widespread than previously noticed and deserves further scrutiny.