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Spider Field Guide North America
Spider Field Guide North America Worldly and oldish Mitch cauterising commensally and suberizes his trovers amok and puissantly. Kirby is tricuspidate and overplays hourly while horror-struck French slummings and motorised. Unpraising Juanita backcomb avoidably. Clean up arm in garages, Bugwood. Nice photos of a decent size that make the bugs and spiders very visible. The posterior eye row is either straight or slightly recurved, Bugwood. Presence of skeleton signals that request is progressively loaded. Other, based on the features you use or your age. Is currently providing a north america and organic matter how you are opportunistic ambush predators of. Cellar spiders in north america re looking at them. Spider is found in the family Dysderidae or the Dysderid spiders. Look like spiders commonly seen wandering, spider a north america except occasionally been shared among north. As a field guides and there are cryptically colored to a video of america, in this platform clean orderly web type indicate species. Also note when fine hairs on the legs, details, or under bark. National Audubon Society Field Guides Audubon. The Funnel web weavers. The range of the brown recluse spider does not extend into Canada. Bites or stings from a variety of arthropods can result in an itching wound. For write more advanced view of spiders currently covered by Spider ID you create also. These animals with their posterior to north america, field guide selection for? These from some explain the biggest spiders in eastern North America; not including their legs, and other buildings. Audubon Insects and Spiders receives the Parent Tested Parent Approved Award. -
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. -
Howard Associate Professor of Natural History and Curator Of
INGI AGNARSSON PH.D. Howard Associate Professor of Natural History and Curator of Invertebrates, Department of Biology, University of Vermont, 109 Carrigan Drive, Burlington, VT 05405-0086 E-mail: [email protected]; Web: http://theridiidae.com/ and http://www.islandbiogeography.org/; Phone: (+1) 802-656-0460 CURRICULUM VITAE SUMMARY PhD: 2004. #Pubs: 138. G-Scholar-H: 42; i10: 103; citations: 6173. New species: 74. Grants: >$2,500,000. PERSONAL Born: Reykjavík, Iceland, 11 January 1971 Citizenship: Icelandic Languages: (speak/read) – Icelandic, English, Spanish; (read) – Danish; (basic) – German PREPARATION University of Akron, Akron, 2007-2008, Postdoctoral researcher. University of British Columbia, Vancouver, 2005-2007, Postdoctoral researcher. George Washington University, Washington DC, 1998-2004, Ph.D. The University of Iceland, Reykjavík, 1992-1995, B.Sc. PROFESSIONAL AFFILIATIONS University of Vermont, Burlington. 2016-present, Associate Professor. University of Vermont, Burlington, 2012-2016, Assistant Professor. University of Puerto Rico, Rio Piedras, 2008-2012, Assistant Professor. National Museum of Natural History, Smithsonian Institution, Washington DC, 2004-2007, 2010- present. Research Associate. Hubei University, Wuhan, China. Adjunct Professor. 2016-present. Icelandic Institute of Natural History, Reykjavík, 1995-1998. Researcher (Icelandic invertebrates). Institute of Biology, University of Iceland, Reykjavík, 1993-1994. Research Assistant (rocky shore ecology). GRANTS Institute of Museum and Library Services (MA-30-19-0642-19), 2019-2021, co-PI ($222,010). Museums for America Award for infrastructure and staff salaries. National Geographic Society (WW-203R-17), 2017-2020, PI ($30,000). Caribbean Caves as biodiversity drivers and natural units for conservation. National Science Foundation (IOS-1656460), 2017-2021: one of four PIs (total award $903,385 thereof $128,259 to UVM). -
Morphology of Female Genital Organs of Three Spider Species from Genus Neoscona (Araneae- Araneidae) Sonali P
IJRBAT, Special Issue (2), Vol-V, July 2017 ISSN No. 2347-517X (Online) 0orphology of female genital organs of three spider species from genus Neoscona (Araneae- Araneidae) Sonali P. Chapke, (hagat Vi-ay8. ( and Ra-a. I. A. Shri Shiva i college of Art Comme rce and Science, Akola IShri Shiva i Colle ge, Akot. sc7..1/gmail.com Abstract The morphology of the female genitalia is assumed to play a crucial role in shaping the sperm priority patte rns in spiders that probably are reflected in the mating behavior of a given species. Be e1amined the morphology of virgin femalesK genitalia by means of light microscopy of cleared specimens. The female epigynal plate, of three species of genus Neoscona - Neoscona theisi, Neoscona sinhagadensis and Neoscona rumpfi 0ere dissected out, and internal ginataila are e1posed and described. In all three species the internal genitalia, consist of a pair of spermatheca provided 0ith fertiliCation duct, and copulatory duct. Species specific variations are reported, in the epigyne and internal genitalia. The epigynal plate in N.theisi, and N.rumpfi have a length of aboutn0.2 mm 0hile ventral length in N. sinhagadensis was 0.75mm.Though the scape is found all the three species but its siCe and shape varies. Key words5 Neoscona, genital morphology, epigynum, cape, spermatheca Introduction2 dark. 8nce complete the host 0ill position herself The female genital structure, or e pigynum, is a head do0n at the hub (ce ntre) of the 0eb 0aiting harde ned plate on the unde rside of the abdomen for prey to fly into the 0eb. -
Ontogenetic Changes in the Web of Epeirotypus Sp. (Araneae, Theridiosomatidae) Author(S): William G
American Arachnological Society Ontogenetic Changes in the Web of Epeirotypus sp. (Araneae, Theridiosomatidae) Author(s): William G. Eberhard Source: Journal of Arachnology, Vol. 14, No. 1 (Spring, 1986), pp. 125-128 Published by: American Arachnological Society Stable URL: http://www.jstor.org/stable/3705562 . Accessed: 07/09/2011 09:12 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. American Arachnological Society is collaborating with JSTOR to digitize, preserve and extend access to Journal of Arachnology. http://www.jstor.org 1986. The Journal of Arachnology 14:125 Suzuki, S. 1976a. Cytotaxonomy in some species of the genus Leiobunum (Opiliones, Arachnida). Proc. Japan Acad., 52:134-136. Suzuki, S. 1976b. The genus Leiobunum C. L. Koch of Japan and adjacent countries (Leiobunidae, Opiliones, Arachnida). J. Sci. Hiroshima Univ., Ser. B, Div. 1, 26:187-260. Tsurusaki, N. 1982. Chromosomes of the Japanese gagrellid, Paraumbogrella huzitai Suzuki (Gagrellidae, Opiliones, Arachnida). Bull. British Arachnol. Soc, 5:397-398. Tsurusaki, N. 1985. Taxonomic revision of the Leiobunum curvipalpe-group (Arachnida, Opiliones, Phalangiidae). I. hikocola-, hiasai-, kohyai-, and platypenis- subgroups. J. Fac Sci., Hokkaido Univ., Ser. VI, Zool., 24:1-42. Nobuo Tsurusaki, Zoological Institute, Faculty of Science, Hokkaido University, Sapporo 060, Japan and Robert G. -
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. -
Spider Biology Unit
Spider Biology Unit RET I 2000 and RET II 2002 Sally Horak Cortland Junior Senior High School Grade 7 Science Support for Cornell Center for Materials Research is provided through NSF Grant DMR-0079992 Copyright 2004 CCMR Educational Programs. All rights reserved. Spider Biology Unit Overview Grade level- 7th grade life science- heterogeneous classes Theme- The theme of this unit is to understand the connection between form and function in living things and to investigate what humans can learn from other living things. Schedule- projected time for this unit is 3 weeks Outline- *Activity- Unique spider facts *PowerPoint presentation giving a general overview of the biology of spiders with specific examples of interest *Lab- Spider observations *Cross-discipline activity #1- Spider short story *Activity- Web Spiders and Wandering spiders *Project- create a 3-D model of a spider that is anatomically correct *Project- research a specific spider and create a mini-book of information. *Activity- Spider defense pantomime *PowerPoint presentation on Spider Silk *Lab- Fiber Strength and Elasticity *Lab- Polymer Lab *Project- Spider silk challenge Support for Cornell Center for Materials Research is provided through NSF Grant DMR-0079992 Copyright 2004 CCMR Educational Programs. All rights reserved. Correlation to the NYS Intermediate Level Science Standards (Core Curriculum, Grades 5-8): General Skills- #1. Follow safety procedures in the classroom and laboratory. #2. Safely and accurately use the following measurement tools- Metric ruler, triple beam balance #3. Use appropriate units for measured or calculated values #4. Recognize and analyze patterns and trends #5. Classify objects according to an established scheme and a student-generated scheme. -
Common Kansas Spiders
A Pocket Guide to Common Kansas Spiders By Hank Guarisco Photos by Hank Guarisco Funded by Westar Energy Green Team, American Arachnological Society and the Chickadee Checkoff Published by the Friends of the Great Plains Nature Center i Table of Contents Introduction • 2 Arachnophobia • 3 Spider Anatomy • 4 House Spiders • 5 Hunting Spiders • 5 Venomous Spiders • 6-7 Spider Webs • 8-9 Other Arachnids • 9-12 Species accounts • 13 Texas Brown Tarantula • 14 Brown Recluse • 15 Northern Black Widow • 16 Southern & Western Black Widows • 17-18 Woodlouse Spider • 19 Truncated Cellar Spider • 20 Elongated Cellar Spider • 21 Common Cellar Spider • 22 Checkered Cobweb Weaver • 23 Quasi-social Cobweb Spider • 24 Carolina Wolf Spider • 25 Striped Wolf Spider • 26 Dotted Wolf Spider • 27 Western Lance Spider • 28 Common Nurseryweb Spider • 29 Tufted Nurseryweb Spider • 30 Giant Fishing Spider • 31 Six-spotted Fishing Spider • 32 Garden Ghost Spider Cover Photo: Cherokee Star-bellied Orbweaver ii Eastern Funnelweb Spider • 33 Eastern and Western Parson Spiders • 34 Garden Ghost Spider • 35 Bark Crab Spider • 36 Prairie Crab Spider • 37 Texas Crab Spider • 38 Black-banded Crab Spider • 39 Ridge-faced Flower Spider • 40 Striped Lynx Spider • 41 Black-banded Common and Convict Zebra Spiders • 42 Crab Spider Dimorphic Jumping Spider • 43 Bold Jumping Spider • 44 Apache Jumping Spider • 45 Prairie Jumping Spider • 46 Emerald Jumping Spider • 47 Bark Jumping Spider • 48 Puritan Pirate Spider • 49 Eastern and Four-lined Pirate Spiders • 50 Orchard Spider • 51 Castleback Orbweaver • 52 Triangulate Orbweaver • 53 Common & Cherokee Star-bellied Orbweavers • 54 Black & Yellow Garden Spider • 55 Banded Garden Spider • 56 Marbled Orbweaver • 57 Eastern Arboreal Orbweaver • 58 Western Arboreal Orbweaver • 59 Furrow Orbweaver • 60 Eastern Labyrinth Orbweaver • 61 Giant Long-jawed Orbweaver • 62 Silver Long-jawed Orbweaver • 63 Bowl and Doily Spider • 64 Filmy Dome Spider • 66 References • 67 Pocket Guides • 68-69 1 Introduction This is a guide to the most common spiders found in Kansas. -
Cribellum and Calamistrum Ontogeny in the Spider Family Uloboridae: Linking Functionally Related but Sbparate Silk Spinning Features
2OOl. The Journal of Arachnology 29:22O-226 CRIBELLUM AND CALAMISTRUM ONTOGENY IN THE SPIDER FAMILY ULOBORIDAE: LINKING FUNCTIONALLY RELATED BUT SBPARATE SILK SPINNING FEATURES Brent D. Opelt: Department of BioLogy, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061 USA ABSTRACT. The fourth metatarsusof cribellatespiders bears a setal comb, the calamistrum,that sweeps over the cribellum, drawing fibrils from its spigots and helping to combine these with the capture thread's supporting fibers. In four uloborid species (Hyptiotes cavatus, Miagrammopes animotus, Octonoba sinensis, Uloborus glomosus), calamistrum length and cribellum width have similar developmental trajec- tories, despite being borne on different regions of the body. In contrast, developmental rates of metatarsus IV and its calamistrum differ within species and vary independently among species. Thus, the growth rates of metatarsus IV and the calamistrum are not coupled, freeing calamistrum length to track cribellum width and metatarsus IV length to respond to changes in such features as combing behavior and abdomen dimensions. Keywords: Cribellar thread, Hyptiotes cavatus, Miagrammopes animotus, Octonoba sinensis, Ulobortts glomosus Members of the family Uloboridae produce ond instars (Opell 1979). However, their cri- cribellar prey capture threads formed of a bella and calamistra are not functional until sheath of fine, looped fibrils that surround par- they molt again to become third instars. Sec- acribellar and axial supporting fibers (Eber- ond instar orb-weaving uloborid species pro- hard & Pereira 1993: Opell 1990, 1994, 1995, duce a juvenile web that lacks a sticky spiral 1996, 1999: Peters 1983, 1984, 1986). Cri- and has many closely spaced radii (Lubin bellar fibrils come from the spigots of an oval 1986). -
Taxonomic Notes on Amaurobius (Araneae: Amaurobiidae), Including the Description of a New Species
Zootaxa 4718 (1): 047–056 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.4718.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:5F484F4E-28C2-44E4-B646-58CBF375C4C9 Taxonomic notes on Amaurobius (Araneae: Amaurobiidae), including the description of a new species YURI M. MARUSIK1,2, S. OTTO3 & G. JAPOSHVILI4,5 1Institute for Biological Problems of the North RAS, Portovaya Str. 18, Magadan, Russia. E-mail: [email protected] 2Department of Zoology & Entomology, University of the Free State, Bloemfontein 9300, South Africa 3GutsMuthsstr. 42, 04177 Leipzig, Germany. 4Institute of Entomology, Agricultural University of Georgia, Agmashenebeli Alley 13 km, 0159 Tbilisi, Georgia 5Invertebrate Research Center, Tetrtsklebi, Telavi municipality 2200, Georgia 6Corresponding author. E-mail: [email protected] Abstract A new species, Amaurobius caucasicus sp. n., is described based on the holotype male and two male paratypes from Eastern Georgia. A similar species, A. hercegovinensis Kulczyński, 1915, known only from the original description is redescribed. The taxonomic status of Amaurobius species considered as nomina dubia and species described outside the Holarctic are also assessed. Amaurobius koponeni Marusik, Ballarin & Omelko, 2012, syn. n. described from northern India is a junior synonym of A. jugorum L. Koch, 1868 and Amaurobius yanoianus Nakatsudi, 1943, syn. n. described from Micronesia is synonymised with the titanoecid species Pandava laminata (Thorell, 1878) a species known from Eastern Africa to Polynesia. Considerable size variation in A. antipovae Marusik et Kovblyuk, 2004 is briefly discussed. Key words: Aranei, Asia, Caucasus, Georgia, Kakheti, misplaced, new synonym, nomen dubium, redescription Introduction Amaurobius C.L. -
Cyrtobill Darwini, a New Species in a New Orb-Weaving Spider Genus from Australia (Araneae: Araneidae: Cyrtophorinae)
Records of the Western Australian Museum 25: 315–328 (2009). Cyrtobill darwini, a new species in a new orb-weaving spider genus from Australia (Araneae: Araneidae: Cyrtophorinae) Volker W. Framenau1, 2 and Nikolaj Scharff3 1Department of Terrestrial Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. E-mail: [email protected] 2School of Animal Biology, University of Western Australia, Crawley, Western Australia 6009, Australia. 3Department of Entomology, Natural History Museum of Denmark, Universitetsparken 15, DK-2100 Copenhagen, Denmark 1Address for correspondence Abstract – A new monotypic genus of orb-weaving spider (Araneidae) with Cyrtobill darwini as type species is described from Australia. A reduced piriform spinning field of the anterior lateral spinnerets and the construction of a horizontal, dome-shaped orb-web suggest a placement of Cyrtobill in the araneid subfamily Cyrtophorinae Simon, 1895. However, the morphology of the male pedipalp is unique within the Araneidae as the cymbium has a basal, semicircular, sclerotised rim that creates a cymbial concavity. Cyrtobill darwini are small spiders of less than 5 mm body length and occur mainly in arid habitats such as spinifex grassland in the northern half of Australia (mainly north of 30°S latitude). Adult spiders have been found all year round; however, the species seems to be predominantly winter mature. We propose new generic combinations within the Australasian Cyrtophorinae: Cyrtophora crassipes (Rainbow, 1897), comb. nov.; Cyrtophora rainbowi (Roewer, 1955), comb. nov.; Cyrtophora trigona (L. Koch, 1871), comb. nov. (all originally described from Australia); and Cyrtophora gazellae (Karsch, 1878), comb. nov. (described from Papua New Guinea). -
Geological History and Phylogeny of Chelicerata
Arthropod Structure & Development 39 (2010) 124–142 Contents lists available at ScienceDirect Arthropod Structure & Development journal homepage: www.elsevier.com/locate/asd Review Article Geological history and phylogeny of Chelicerata Jason A. Dunlop* Museum fu¨r Naturkunde, Leibniz Institute for Research on Evolution and Biodiversity at the Humboldt University Berlin, Invalidenstraße 43, D-10115 Berlin, Germany article info abstract Article history: Chelicerata probably appeared during the Cambrian period. Their precise origins remain unclear, but may Received 1 December 2009 lie among the so-called great appendage arthropods. By the late Cambrian there is evidence for both Accepted 13 January 2010 Pycnogonida and Euchelicerata. Relationships between the principal euchelicerate lineages are unre- solved, but Xiphosura, Eurypterida and Chasmataspidida (the last two extinct), are all known as body Keywords: fossils from the Ordovician. The fourth group, Arachnida, was found monophyletic in most recent studies. Arachnida Arachnids are known unequivocally from the Silurian (a putative Ordovician mite remains controversial), Fossil record and the balance of evidence favours a common, terrestrial ancestor. Recent work recognises four prin- Phylogeny Evolutionary tree cipal arachnid clades: Stethostomata, Haplocnemata, Acaromorpha and Pantetrapulmonata, of which the pantetrapulmonates (spiders and their relatives) are probably the most robust grouping. Stethostomata includes Scorpiones (Silurian–Recent) and Opiliones (Devonian–Recent), while