Module 5 Spiders
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Spiders (Araneae) of Stony Debris in North Bohemia
Arachnol. Mitt. 12:46-56 Basel, Dezember 1996 Spiders (Araneae) of stony debris in North Bohemia o v v Vlastimil RUZICKA & Jaromfr HAJER Abstract: The arachnofauna was studied at five stony debris sites in northern Bohemia. In Central Europe, the northern and montane species inhabiting cold places live not only on mountain tops and peat bogs but also on the lower edges of boulder debris, where air streaming through the system of inner compartments gives rise to an exceedingly cold microclimate. At such cold sites, spiders can live either on bare stones (Bathyphantes simillimus, Wubanoides ura/ensis), or in the rich layers of moss and lichen (Dip/oeentria bidentata). Kratoehviliella bieapitata exhibits a diplostenoecious occurrence in stony debris and on tree bark. Latithorax faustus and Theonoe minutissima display diplostenoecious occurrence in stony debris and on peat bogs. The occurrence of the species Seotina eelans in the Czech Republic was documented for the first time. Key words: Spiders, stony debris, microclimate, geographic distribution. INTRODUCTION Stony debris constitute, in Central Europe, island ecosystems which have remained virtually intact over the entire Holocene. Due to the unfeasibility of utilization, stony debris areas are among the few ecosystems that have only minimally been affected by man. In bulky accumulations, air can flow through the system of internal spaces. In this way, cold air can accumulate in the lower part of the tal us, so that ice can form and persist there until late spring. This phenomenon, well known from the Alp region (FURRER 1966), occurs widely in North Bohemia (KUBAT 1971). Owing to the specific substrate and microclimate, stony debris areas are inhabited by specific plant (SADLO & KOLBEK 1994) and animal communities, contributing thus o v v significantly to the biodiversity of the landscape (RUZICKA 1993a). -
Family Practice
THE JOURNAL OF FAMILY ONLINE EXCLUSIVE PRACTICE Paul K. Carlton, Jr, MD, Brown recluse spider bite? FACS The Texas A&M University Consider this uniquely Health Science Center College Station, Tex conservative treatment [email protected] An antihistamine and observation work as well— and often better—than more intensive therapies. Practice recommendations oped it in 4 phases, which I describe in • Be concerned about brown recluse this article. Not only does this conser- envenomation when a patient vative approach consistently heal con- reports intensifying localized firmed brown recluse bite wounds, but pain disproportionate to physical should a bite be mistakenly attributed findings after a “bite” (C). to the brown recluse (or one of its rela- tives in the Loxosceles genus of spider), • Prescribe an oral antihistamine there is no harm to the patient, nor any alone to control symptoms, even big expense. with a necrotic wound, and mark the IN THIS ARTICLE patient’s progress over 24 hours (C). z Spider bite z Is a brown recluse • If the patient improves dramatically, to blame? or MRSA? continue the antihistamine; with little Due to limited experience among the Page E6 or no improvement, consider giving an wider medical community in identifying antibiotic with the antihistamine (C). spider envenomation,1-4 bite recognition and selection of appropriate therapy can Strength of recommendation (SOR) be difficult. A Good-quality patient-oriented evidence Early findings can be confusing. B Inconsistent or limited-quality patient-oriented evidence C Consensus, usual practice, opinion, disease-oriented Brown recluse bites typically feel like a evidence, case series pin prick. -
Untangling Taxonomy: a DNA Barcode Reference Library for Canadian Spiders
Molecular Ecology Resources (2016) 16, 325–341 doi: 10.1111/1755-0998.12444 Untangling taxonomy: a DNA barcode reference library for Canadian spiders GERGIN A. BLAGOEV, JEREMY R. DEWAARD, SUJEEVAN RATNASINGHAM, STEPHANIE L. DEWAARD, LIUQIONG LU, JAMES ROBERTSON, ANGELA C. TELFER and PAUL D. N. HEBERT Biodiversity Institute of Ontario, University of Guelph, Guelph, ON, Canada Abstract Approximately 1460 species of spiders have been reported from Canada, 3% of the global fauna. This study provides a DNA barcode reference library for 1018 of these species based upon the analysis of more than 30 000 specimens. The sequence results show a clear barcode gap in most cases with a mean intraspecific divergence of 0.78% vs. a min- imum nearest-neighbour (NN) distance averaging 7.85%. The sequences were assigned to 1359 Barcode index num- bers (BINs) with 1344 of these BINs composed of specimens belonging to a single currently recognized species. There was a perfect correspondence between BIN membership and a known species in 795 cases, while another 197 species were assigned to two or more BINs (556 in total). A few other species (26) were involved in BIN merges or in a combination of merges and splits. There was only a weak relationship between the number of specimens analysed for a species and its BIN count. However, three species were clear outliers with their specimens being placed in 11– 22 BINs. Although all BIN splits need further study to clarify the taxonomic status of the entities involved, DNA bar- codes discriminated 98% of the 1018 species. The present survey conservatively revealed 16 species new to science, 52 species new to Canada and major range extensions for 426 species. -
How Non-Nestmates Affect the Cohesion of Swarming Groups in Social Spiders
Insect. Soc. 55 (2008) 355 – 359 0020-1812/08/040355-5 Insectes Sociaux DOI 10.1007/s00040-008-1011-8 Birkhäuser Verlag, Basel, 2008 Research article How non-nestmates affect the cohesion of swarming groups in social spiders A.-C. Mailleux1, R. Furey2, F. Saffre1, B. Krafft4 and J.-L. Deneubourg1 1 Service dÉcologie Sociale, Campus de la Plaine, CP 231, UniversitØ Libre de Bruxelles, 1050 Brussels, Belgium, e-mail: [email protected], [email protected], [email protected] 2 Harrisburg University of Science and Technology 866, HBG.UNIV 215, Market Street, Harrisburg, Pennsylvania 17101 USA, e-mail: [email protected] 3 UniversitØ Nancy 2, Rue Baron Louis, BP 454 Code postal 54001 Ville Nancy Cedex, France, e-mail: [email protected] Received 30 October 2007; revised 3 April and 19 May 2008; accepted 22 May 2008. Published Online First 17 June 2008 Abstract. In social biology, it is often considered that an Fletcher and Michener, 1987). Unlike most vertebrate organized society cannot exist without exclusion behav- and invertebrate societies (Hepper, 1986; Fletcher and iour towards newcomers from another nest. Unlike most Michener, 1987), social spiders accept artificially intro- vertebrate and invertebrate social species, social spiders duced immigrants without apparent discrimination or such as Anelosimus eximius accept unrelated migrants agonistic behaviour (Evans, 1999). This absence of group without agonistic behaviour. Does it imply that spiders closure prompts some authors to suggest that spiders cannot recognize non-nestmates from nestmates or is cannot identify newcomers (Buskirk, 1981; Howard, there any evidence of recognition without aggression ? In 1982; Darchen and Delage-Darchen, 1986; Pasquet et order to answer this question, we studied behavioural al., 1997). -
The Road Travelled by Australian Trapdoor Spiders
Discovered words and photo by Mark Harvey, WA Museum ustralia is home to many unique spiders with most species occurring Anowhere else on Earth. Many have their origins in the distant past, when Australia was part of Gondwana in the Mesozoic, ca. 180 million years ago. Australia, New Zealand, South America, Africa, Madagascar, Antarctica and the Indian sub-continent, plus a few small islands, once formed a massive southern supercontinent known as Gondwana that gradually fragmented from the Jurassic, ca. 180–160 million years ago. Evidence of the connection between these continental blocks can be found in the fossil record The road travelled by Australian of some plants and animals, but most strikingly in the presence of related groups trapdoor spiders of organisms in the modern biota. But back to spiders. There are three major groups of spiders: the Mesothelae (a Australia that lives in shallow burrows with Above An undescribed species of Conothele. group of primitive spiders now only found in a flap-like lid. It was discovered by Adelaide Asia), the Mygalomorphae (trapdoor spiders University PhD student, Sophie Harrison, and their relatives) and the Araneomorphae to be most closely related to spiders of (all other spiders). The Australian the same genus from South Africa. Using timeline of Australia bumping into Asia. mygalomorphs include trapdoor, funnel- molecular sequence data, Sophie found that He also noted that there were two distinct web and mouse spiders, and tarantulas. the spider, Moggridgea rainbowi, diverged habitat preferences for Australian Conothele. Most Australian mygalomorph spiders from its African cousins sometime between Some species built burrows on tree trunks have their origins in Gondwana. -
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. -
Prey of the Jumping Spider Phidippus Johnsoni (Araneae : Salticidae)
Jackson, R. R . 1977 . Prey of the jumping spider Phidippus johnsoni (Araneae : Salticidae) . J. Arachnol. 5 :145-149 . PREY OF THE JUMPING SPIDER PHIDIPPUS JOHNSONI (ARANEAE : SALTICIDAE) Robert R. Jackson I Zoology Departmen t University of Californi a Berkeley, California 9472 0 ABSTRACT Field data indicate that P. johnsoni is an euryphagous predator, whose diet includes organisms (aphids, ants, opilionids) sometimes considered distasteful to spiders . Other spiders are preyed upon , including conspecifics. Prey size tends to be one quarter to three quarters the size of the predator . INTRODUCTION Since spiders are probably a dominant group of predators of insects (Bristowe, 1941 ; Riechert, 1974; Turnbull, 1973), there is considerable interest in their feeding ecology . Spiders have usually been considered to be euryphagous predators with a stabilizing , rather than regulative, effect on insect populations (Riechert, 1974) . However, informa- tion concerning the prey taken by particular spider species, in the field, is limited . Field studies by Edgar (1969, 1970), Robinson and Robinson (1970) and Turnbull (1960) are especially noteworthy . During the course of a study of the reproductive biology of Phidippus johnsoni (Peckham and Peckham) (Jackson, 1976), occasionally individuals of this species were found in the field holding prey in their chelicerae . Each prey discovered in this way i s listed in Table 1 . In addition, Ken Evans and Charles Griswold, who were familiar wit h this species, recorded observations of P. johnsoni with prey. (Their data are included in Table 1 .) These data came from a variety of habitats in western North America, most o f which have been described elsewhere (Jackson, 1976) . -
North American Spiders of the Genera Cybaeus and Cybaeina
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by The University of Utah: J. Willard Marriott Digital... BULLETIN OF THE UNIVERSITY OF UTAH Volume 23 December, 1932 No. 2 North American Spiders of the Genera Cybaeus and Cybaeina BY RALPH V. CHAMBERLIN and WILTON IVIE BIOLOGICAL SERIES, Vol. II, No. / - PUBLISHED BY THE UNIVERSITY OF UTAH SALT LAKE CITY THE UNIVERSITY PRESS UNIVERSITY OF UTAH SALT LAKE CITY A Review of the North American Spider of the Genera Cybaeus and Cybaeina By R a l p h V. C h a m b e r l i n a n d W i l t o n I v i e The frequency with which members of the Agelenid genus Cybaeus appeared in collections made by the authors in the mountainous and timbered sections of the Pacific coast region and the representations therein of various apparently undescribed species led to the preparation of this review of the known North American forms. One species hereto fore placed in Cybaeus is made the type of a new genus Cybaeina. Most of our species occur in the western states; and it is probable that fur ther collecting in this region will bring to light a considerable number of additional forms. The drawings accompanying the paper were made from specimens direct excepting in a few cases where material was not available. In these cases the drawings were copied from the figures published by the authors of the species concerned, as indicated hereafter in each such case, but these drawings were somewhat revised to conform with the general scheme of the other figures in order to facilitate comparison. -
Taxonomic Notes on Agroeca (Araneae, Liocranidae)
Arachnol. Mitt. 37: 27-30 Nürnberg, Juli 2009 Taxonomic notes on Agroeca (Araneae, Liocranidae) Torbjörn Kronestedt Abstract: Agroeca gaunitzi Tullgren, 1952 is stated here to be a junior synonym of A. proxima (O. P.-Cambridge, 1871). The illustrations of the male palp attributed to A. proxima in papers by Tullgren of 1946 and 1952 in fact show A. inopina O. P.-Cambridge, 1886. The record of A. inopina from Finland, quite outside its known distribution range, was based on a misidentification. It is argued that the type species of the genus Agroeca Westring, 1861 should be A. proxima (O. P.-Cambridge, 1871), not A. brunnea (Blackwall, 1833) as currently applied. Protagroeca Lohmander, 1944 is placed as an objective synonym of Agroeca Westring, 1861. Key words: Agroeca gaunitzi, synonyms, type species On the identity of Agroeca gaunitzi Tullgren, 1952 Because Agroeca gaunitzi still appears as a valid Agroeca gaunitzi was described based on a single nominal species (HELSDINGEN 2009, PLATNICK male from the southern part of Swedish Lapland 2009), a re-study of the holotype was undertaken in (TULLGREN 1952). No additional specimens have order to clarify its identity. As a result, the following since been assigned to this nominal species and it conclusions were reached: was not mentioned in the most recent taxonomical revision of the genus (GRIMM 1986) nor in the 1. The holotype of Agroeca gaunitzi is a male of latest treatment of the family in Sweden (ALM- Agroeca proxima, thus making the former a junior QUIST 2006). synonym, syn. n. According to the original description, A. gau- 2. -
Approach and Management of Spider Bites for the Primary Care Physician
Osteopathic Family Physician (2011) 3, 149-153 Approach and management of spider bites for the primary care physician John Ashurst, DO,a Joe Sexton, MD,a Matt Cook, DOb From the Departments of aEmergency Medicine and bToxicology, Lehigh Valley Health Network, Allentown, PA. KEYWORDS: Summary The class Arachnida of the phylum Arthropoda comprises an estimated 100,000 species Spider bite; worldwide. However, only a handful of these species can cause clinical effects in humans because many Black widow; are unable to penetrate the skin, whereas others only inject prey-specific venom. The bite from a widow Brown recluse spider will produce local symptoms that include muscle spasm and systemic symptoms that resemble acute abdomen. The bite from a brown recluse locally will resemble a target lesion but will develop into an ulcerative, necrotic lesion over time. Spider bites can be prevented by several simple measures including home cleanliness and wearing the proper attire while working outdoors. Although most spider bites cause only local tissue swelling, early species identification coupled with species-specific man- agement may decrease the rate of morbidity associated with bites. © 2011 Elsevier Inc. All rights reserved. More than 100,000 species of spiders are found world- homes and yards in the southwestern United States, and wide. Persons seeking medical attention as a result of spider related species occur in the temperate climate zones across bites is estimated at 50,000 patients per year.1,2 Although the globe.2,5 The second, Lactrodectus, or the common almost all species of spiders possess some level of venom, widow spider, are found in both temperate and tropical 2 the majority are considered harmless to humans. -
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. -
Araneae) Parasite–Host Association
2006. The Journal of Arachnology 34:273–278 SHORT COMMUNICATION FIRST UNEQUIVOCAL MERMITHID–LINYPHIID (ARANEAE) PARASITE–HOST ASSOCIATION David Penney: Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, UK. E-mail: [email protected] Susan P. Bennett: Biological Sciences, Manchester Metropolitan University, Manchester, M1 5GD, UK. ABSTRACT. The first description of a Mermithidae–Linyphiidae parasite–host association is presented. The nematode is preserved exiting the abdomen of the host, which is a juvenile Tenuiphantes species (Araneae, Linyphiidae), collected from the Isle of Mull, UK. An updated taxonomic list of known mer- mithid spider hosts is provided. The ecology of known spider hosts with regard to the direct and indirect life cycles of mermithid worms suggests that both occur in spiders. Keywords: Aranimermis, Isle of Mull, Linyphiidae, Mermithidae, Nematoda Nematode parasites of spiders are restricted to an updated and taxonomically correct list in Table the family Mermithidae but are not uncommon 1. Here we describe the first Mermithidae–Liny- (Poinar 1985, 1987) and were first reported almost phiidae parasite–host association and discuss the two and a half centuries ago (Roesel 1761). How- ecology of known spider hosts with regard to the ever, given the difficulty of identifying and rearing life cycles of mermithid worms. post-parasitic juvenile mermithids, they have re- This paper concerns three spider specimens, one ceived inadequate systematic treatment (Poinar with a worm in situ and two that are presumed to 1985). In addition, the complete life history is have been parasitized, but from which the worms known for only one species of these spider parasites have emerged and are lost.