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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. -
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. -
The Jumping Spiders (Araneae: Salticidae) of the Virginia Peninsula1
Vol. 98, No. 5, November & December 1987 235 THE JUMPING SPIDERS (ARANEAE: SALTICIDAE) OF THE VIRGINIA PENINSULA 1 2 C.L. Stietenroth, N.V. Horner ABSTRACT: Thirty species representing 1 8 genera of Salticidae are recorded from the Virginia Peninsula. Habitat and natural history information for each species is presented. Some salticids on the peninsula occupy diverse habitats while other species appear to confine themselves to more restricted environments. The most abundant salticid was Hentzia palmarum. Metaphi- dippus galathea and Platycryptus undatus were most widely distributed species. Salticids reported in Virginia for the first time are Phidippus princeps, P. otiosus, Thiodina sylvana, Sitticus fasciger and Zygoballus sexpunctatus. A few studies concerning the spider fauna of Virginia have been published. The earliest record of occurrence was by John Banister between 1678 and 1692 (Ewan and Ewan, 1970). More recently, McCaffrey and Hornsburgh published three studies concerning spiders in apple orchards in central Virginia. Their assessment of spider populations in an unsprayed orchard was published in 1 1 977 followed ( 978) by laboratory feeding studies performed to evaluate potential effects of predaceous spiders on insect residents of apple orchards. Later (1980), a comparison was made between the spider populations in abandoned and commercial orchards; 68 species were identified. Dowd and Kok (1981), and McPherson el al. (1982) considered spider and other arthropod predation on the curculionid beetle, Rhynocyllus sp., in a in 1 soybean cropping system Virginia. Holsinger ( 982) reported on the spider cave-fauna in Burnsville Cove. The efficiency of limb-beating for capturing various spider families in apple orchards is discussed by McCaffrey and Parrella(1984). -
Visual Reactions to Auditory Stimulus by the Jumping Spider Phidippus Princeps (Araneae, Salticidae)
Visual reactions to auditory stimulus by the jumping spider Phidippus princeps (Araneae, Salticidae) Philip Denbaum Degree project in biology, Master of science (2 years), 2019 Examensarbete i biologi 45 hp till masterexamen, 2019 Biology Education Centre, Uppsala University, and Elizabeth Jakob lab, University of Massachusetts Supervisors: Elizabeth Jakob and Anders Berglund External opponent: Emilie Laurent & Julian Baur Table of contents Abstract 2 Introduction 3 Methods and Materials 5 Spider collection and care 5 General experimental setup 5 Overview of the eyetracker 5 Securing the spider 6 Aligning spider and finding retinas 6 Experiment 7 Data analysis 8 Statistical analyses 9 Results 10 Analysis 1 10 Analysis 2 13 Discussion 14 Future studies 15 Conclusions 16 Acknowledgements 16 References 17 Appendix 19 !1 Abstract Jumping spiders (Family Salticidae) are known for their exceptional vision, including color vision and spatial acuity. Salticids use their vision in many behaviors, including predation and courtship. Recently evidence of their ability to sense airborne vibrations, i.e. sound, was published. I used a specialized jumping-spider-specific eyetracker to study the visual reaction of the retinas of the jumping spider Phidippus princeps when exposed to the sound of a predator. I used a generic wasp sound, previously shown to induce a startle response, as stimulus and played it from different directions. The spiders showed strong reactions to the sound stimulus by large increases in retinal movement when exposed to the stimulus, and they showed no habituation to the stimulus over three rounds of exposure. However, I found no indication that the direction of retinal movement corresponded to the location of the sound source. -
Shale Hollow Preserve Bio Blitz May 15-16, 2015
Shale Hollow Preserve Bio Blitz May 15-16, 2015 SCIENTIFIC NAME COMMON NAME Terrestrial Insect Vanessa atalanta Red Admiral Cicindela sexguttata Tiger Beetle Malacosoma americanum Eastern Tent Caterpillar Pieris rapae Cabbage White Lycaena hyllus Bronze Copper Papilio glaucus Eastern Tiger Swallowtail Epargereus clarus Silver-spotted Skipper Cicindela sexguttata Six-spotted Tiger Beetle Phyciodes tharos Pearl Crescent Nicrophorus orbicollis Roundneck Sexton Beetle Aquatic Macroinvertebrates Allocapnia spp. Stonefly Nymph Aquatic Invertebrates Sphaeriidae spp. Fingernail Clam Phreatoious spp. Freshwater Isopod Limnephilus spp. Northern Caddisfly Mammals Sciurus carolinensis Eastern Gray Squirrel Sciurus niger Fox Squirrel Microtus pennsylvanicus Meadow Vole Odocoileus virginianus White-tailed Deer Tamias striatus Eastern Chipmunk Amphibians Anaxyrus americanus American Toad Desmognathus fuscus Dusky Salamander Hyla versicolor Gray Tree Frog Lithobates clamitans Green Frog Eurycea bislineata Northern Two - lined Salamander Plethodon cinereus Red-backed Salamander Woody Plants Cornus alternifolia Alternate-leaved Dogwood Cornus florida Flowering Dogwood Gaylussacia baccata Black Huckleberry Prunus serotina Black Cherry Rosa multiflora Multiflora Rose Lonicera spp. Bush Honey Suckle Acer sacchrum Sugar Maple Ulmus americana American elm Ligustrum vulgare Common privet Berberis vulgaris European barberry Smilax spp. Greenbrier Lendara benzoin Common Spicebush Viburnum lentago Nannyberry Viburnum Rubus idaeus Red Rasberry Hamamelis virginiana -
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. -
Synanthropic Salticidae of the Northeast United States
PECKHAMIA 64.1, 8 September 2008 ISSN 1944-8120 This is a PDF version of PECKHAMIA 2(6): 91-92, December 1990. Pagination of the original document has been retained. Editor's note (64.1): Euophrys erratica is now known as Pseudeuophrys erratica (Zabka, M., 1997, Fauna Polski 19: 5-187), Habrocestum pulex as Naphrys pulex (Edwards, G. B., 2002, Insecta Mundi 16(1-3): 65-74). and Metaphidippus canadensis as Ghelna canadensis (Maddison, W. P., 1996, Bull. Mus. Comp. Zool. 154(4): 215-368). 91 SYNANTHROPIC SALTICIDAE OF THE NORTHEAST UNITED STATES Bruce Cutler 1966 Eustis St., Lauderdale, MN 55113 This paper is based on my collecting experience primarily in New York, New Jersey, northern Illinois, and Minnesota, with lesser collecting in Wisconsin and Michigan. There is some input from the observations of others, and from the literature. Kaston (1983) has a useful summary of other observations. I have divided the synanthropic species into different categories based on mode of occurrence and probable area of origin. The first group of species is what are considered to be the classic examples of synanthropic species. That is, nonnative species exclusively associated with human structures. There are two widespread species in this region. Salticus scenicus (Clerck) was undoubtedly introduced from western Europe, and occurs in every metropolitan area in the northeast United States, and in many small towns as well. In some places, it has spread to non-synanthropic habitats. Except for scattered records from trees (i. e. Jennings and Collins 1987), the rest are from bare rock areas- rocky shores of Lake Superior in the Upper Peninsula of Michigan, limestone cliffs in the Twin cities of Minnesota, and on a quartzite ridge in southwest Minnesota. -
Common Spiders of the Chicago Region 1 the Field Museum – Division of Environment, Culture, and Conservation
An Introduction to the Spiders of Chicago Wilderness, USA Common Spiders of the Chicago Region 1 The Field Museum – Division of Environment, Culture, and Conservation Produced by: Jane and John Balaban, North Branch Restoration Project; Rebecca Schillo, Conservation Ecologist, The Field Museum; Lynette Schimming, BugGuide.net. © ECCo, The Field Museum, Chicago, IL 60605 USA [http://fieldmuseum.org/IDtools] [[email protected]] version 2, 2/2012 Images © Tom Murray, Lynette Schimming, Jane and John Balaban, and others – Under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License (non-native species listed in red) ARANEIDAE ORB WEAVERS Orb Weavers and Long-Jawed Orb Weavers make classic orb webs made famous by the book Charlotte’s Web. You can sometimes tell a spider by its eyes, most have eight. This chart shows the orb weaver eye arrangement (see pg 6 for more info) 1 ARANEIDAE 2 Argiope aurantia 3 Argiope trifasciata 4 Araneus marmoreus Orb Weaver Spider Web Black and Yellow Argiope Banded Argiope Marbled Orbweaver ORB WEAVERS are classic spiders of gardens, grasslands, and woodlands. The Argiope shown here are the large grassland spiders of late summer and fall. Most Orb Weavers mature in late summer and look slightly different as juveniles. Pattern and coloring can vary in some species such as Araneus marmoreus. See the link for photos of its color patterns: 5 Araneus thaddeus 6 Araneus cingulatus 7 Araneus diadematus 8 Araneus trifolium http://bugguide.net/node/view/2016 Lattice Orbweaver Cross Orbweaver Shamrock Orbweaver 9 Metepeira labyrinthea 10 Neoscona arabesca 11 Larinioides cornutus 12 Araniella displicata 13 Verrucosa arenata Labyrinth Orbweaver Arabesque Orbweaver Furrow Orbweaver Sixspotted Orbweaver Arrowhead Spider TETRAGNATHIDAE LONG-JAWED ORB WEAVERS Leucauge is a common colorful spider of our gardens and woodlands, often found hanging under its almost horizontal web. -
Shale Hollow Park Bioblitz
Shale Hollow Park BioBlitz May 15-16, 2015 SCIENTIFIC NAME COMMON NAME Mammals Sciurus carolinensis Eastern Gray Squirrel Sciurus niger Fox Squirrel Microtus pennsylvanicus Meadow Vole Odocoileus virginianus White-tailed Deer Tamias striatus Eastern Chipmunk Birds Contopus Virens Eastern Wood-Pewee Vireo olivaceus Red-eyed Vireo Buteo jamaicensis Red-tailed Hawk Piranga olivacae Scarlet Tanager leuconotopicus villosus Hairy Woodpecker Turdus migratorious American Robin Spizella passerina Chipping Sparrow Dumetella carolinensis Gray Catbird Poecile carolinensis Carolina Chickadee Polioptila caerulea Blue-gray Gnatcatcher Cardinalis cardinalis Northern Cardinal Colaptes auratus Northern Flicker Setophaga ruticilla American Redstart Cyanocitta cristata Blue Jay Zenaida Macroura Mourning Dove Chordeiles minor Common Nighthawk Corvus brachyrhynchos American Crow Sayornis phoebe Eastern Phoebe Pipilo erythrophthalmus Eastern Towhee Empidonax virescens Acadian Flycatcher Baeolophus bicolor Tufted Titmouse Hylocichla mustelina Wood Thrush Hylatomus pileatus Pileated Woodpecker Parkesia motacilla Louisiana Waterthrush Ardea herodias Great Blue Heron Setophaga americana Northern Parula Catharus guttatus Hermit Thrush Passerina cyanae Indigo Bunting Lcterus galbula Baltimore Oriole Picoides pubescens Downy Woodpecker 1 of 5 Shale Hollow Park BioBlitz May 15-16, 2015 SCIENTIFIC NAME COMMON NAME MammalsMelanerpes carolinus Red-bellied Woodpecker Geothlypis trichas Common Yellowthroat Catharus ustulatus Swainson's Thrush Durnetella carolinensis Gray -
Dimorphic Jumper Maevia Inclemens (Walckenaer 1837) (Arachnida: Araneae: Salticidae)1 Laurel Lietzenmayer and Lisa Taylor2
EENY-702 Dimorphic Jumper Maevia inclemens (Walckenaer 1837) (Arachnida: Araneae: Salticidae)1 Laurel Lietzenmayer and Lisa Taylor2 Introduction Description Maevia inclemens is a common jumping spider (Family Maevia inclemens is a medium-sized jumping spider with Salticidae) distributed throughout eastern North America, females larger than males. Females are 6.5–10.0 mm and primarily found along tree lines in vines and ivy (Bradley males are 4.8–7.0 mm in total body length (Bradley 2012). 2012). Like most jumping spiders, Maevia inclemens is Females have a white face and two red or black lines down a voracious generalist predator that feeds on a variety of the back of their abdomens (Bradley 2012, Figure 2). The small insects and other arthropods. Curiously, Maevia tufted morph is characterized by three tufts of hair that inclemens is the only known jumping spider (from a family protrude from their head, with a black body, and white of nearly 6,000 species) (World Spider Catalog 2017) legs (Figure 3A–B). The striped morph (known commonly to have dimorphic males; these two types of males (or as the gray morph) has yellow pedipalps (small append- morphs) differ in both morphology and courtship behavior ages near their face), black-and-white striped legs, and a and are found in roughly equal frequency in a population grey abdomen with subtle orange markings (Clark and (Clark and Uetz 1990). Uetz 1993; Clark and Morjan 2001, Figure 1, 3C–D). It is currently unknown what factors determine which morph a male will become, and it is difficult to predict what morph a juvenile spider will become as an adult. -
Signal Efficacy and the Evolution of Male Dimorphism in the Jumping Spider, Maevia Inclemens (Video/Communication/Mate Recognition/Sensory Exploitation) DAVID L
Proc. Natl. Acad. Sci. USA Vol. 90, pp. 11954-11957, December 1993 Evolution Signal efficacy and the evolution of male dimorphism in the jumping spider, Maevia inclemens (video/communication/mate recognition/sensory exploitation) DAVID L. CLARK* AND GEORGE W. UETZ Department of Biological Sciences, University of Cincinnati, Cincinnati, OH 45221 Communicated by Peter Marler, September 7, 1993 ABSTRACT An extreme form of male dimorphism occurs morphism is likely because within the genus Maevia, Maevia in the jumping spider, Maevia inclemens, where two male inclemens is the only member to exhibit this type of male morphs differ dramatically in both morphology and behavior. dimorphism, and other males within the genus resemble and We examined the visual signals transmitted to females by the behave much like the gray morph of M. inclemens. Also, in two different morphs during courtship display. Even though M. inclemens, all juveniles resemble the adult gray morph the display of each male is different, as a function of behavior and are not distinguishable as different male morphs until and courtship distance, the males present females with images their final molt. that are almost identical in height and visual target area. By An earlier study proposed that dimorphic males evolved by substituting live males with computer-animated sequences of sexual selection through female choice (8), where females male courtship behavior, the male morphs were superimposed were presumed to have a mating preference for the tufted upon each other, and females were determined to have two morph. However, it was recently demonstrated that mate distinct male-recognition templates. We hypothesize that the selection is independent of male morphology (11) and that dimorphic males of this species evolved through sensory ex- female M. -
PECKHAMIA 60.1, 5 September 2008 ISSN 1944-8120 Since Collections
PECKHAMIA 60.1, 5 September 2008 ISSN 1944-8120 This is a PDF version of PECKHAMIA 2(4): 49-57, December 1984. Pagination of the original document has been retained. 49 AN ANNOTATED LIST OF SOUTH CAROLINA SALTICIDAE (ARANEAE). S. H. Roach and G. B. Edwards The occurrence of jumping spiders (Salticidae) as a group has not previously been reported for the state of South Carolina. Numerous records of individual species collected in the state are scattered throughout the literature but often the records and the identifications are questionable, especially in light of recent revisions of several important genera. In this report we present the results of several years collection of salticids in the state of South Carolina, and a listing of species which may occur, but have not been collected by us, or else have been reported as occurring in the state by other workers (indicated by an asterisk). Extensive use of the lists published by Richman and Cutler (1978) and Kaston (1980) has been made in formulating this report. Griswold's (1983) revision of Habronattus when published will undoubtedly change what we now know about this genus. 50 Since collections in the mountains and along the Georgia-South Carolina border have been limited, numerous species may be present which we have not collected, and these may be reported later if warranted. In all, about 80 species of salticids are known or suspected to occur in South Carolina at this time. *Admestina tibialis (C. L. Koch). Reported from Georgia (Edwards & Rossman 1981) from Habersham County (in mountainous region). Agassa cyanea (Hentz).