PECKHAMIA 60.1, 5 September 2008 ISSN 1944-8120 Since Collections
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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. -
SPIDERS of WASHINGTON COUNTY, MISSISSIPPI Orrey P. Young Southern Field Crop Insect Management Laboratory USDA-ARS, P.O. Box
Young, O . P., T. C . Lockley and G . B . Edwards . 1989 . Spiders of Washington County, Mississippi . J . Arachnol ., 17 :27-41 . SPIDERS OF WASHINGTON COUNTY, MISSISSIPPI Orrey P. Young Southern Field Crop Insect Management Laboratory USDA-ARS, P.O. Box 346 Stoneville, Mississippi 38776 USA Timothy C. Lockley Imported Fire Ant Station USDA-APHIS-PPQ 3505 25th Avenue Gulfport, Mississippi 39501 USA and G. B. Edwards Florida State Collection of Arthropods Division of Plant Industry Florida Dept. Agric. & Cons . Serv. P.O. Box 1269 Gainesville, Florida 32602 USA ABSTRACT Over a seven-year period, approximately 35,000 spiders representing 26 families, 133 genera, and 234 species were captured in Washington County, Mississippi, by pitfall, sweepnet, vacuum, bag, and hand. Specimens were collected in 10 different habitat types and in four vegetational strata . Old-field habitats yielded the most species (152) and residential lawns the fewest (14) . Considering all habitats sampled, the ground layer produced 111 species, the herbaceous strata 133, the shrub layer 49, and the tree strata 30 species . The sweepnet method of capture obtained 128 species, pitfall 95, hand 61, vacuum 53, and bagging 19 species. The largest number of species were obtained in spring and early summer (maximum of 125 in May), with the fewest in mid-winter (Jan . = 24) . Twenty-one species were considered abundant, 51 common, 67 uncommon, and 95 rare . Additions to the state list of Dorris (1972) number 102 species, for a new state total of 364 species . A comparison with the North American fauna and with other surveys indicates that Washington County is underrepresented both in cursorial forms active on the soil surface and web-spinning forms typical of undisturbed habitats . -
Evolutionary Divergences Mirror Pleistocene Paleodrainages in A
Molecular Phylogenetics and Evolution 144 (2020) 106696 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Evolutionary divergences mirror Pleistocene paleodrainages in a rapidly- T evolving complex of oasis-dwelling jumping spiders (Salticidae, Habronattus tarsalis) ⁎ Marshal Hedina, , Steven Foldia,b, Brendan Rajah-Boyera,c a Dept of Biology, San Diego State University, San Diego, CA 92182, United States b Valley International Prep School, Chatsworth, CA 91311, United States c St. Francis of Assisi Catholic School, Vista, CA 92083, United States ARTICLE INFO ABSTRACT Keywords: We aimed to understand the diversifcation history of jumping spiders in the Habronattus tarsalis species com- Biogeography plex, with particular emphasis on how history in this system might illuminate biogeographic patterns and Ephemeral speciation processes in deserts of the western United States. Desert populations of H. tarsalis are now confned to highly Introgression discontinuous oasis-like habitats, but these habitats would have been periodically more connected during Pleistocene multiple pluvial periods of the Pleistocene. We estimated divergence times using relaxed molecular clock ana- Saline Valley lyses of published transcriptome datasets. Geographic patterns of diversifcation history were assessed using Sexual selection phylogenetic and cluster analyses of original sequence capture, RADSeq and morphological data. Clock analyses of multiple replicate transcriptome datasets suggest mid- to late-Pleistocene divergence dates within the H. tarsalis group complex. Coalescent and concatenated phylogenetic analyses indicate four early-diverging lineages (H. mustaciata, H. ophrys, and H. tarsalis from the Lahontan and Owens drainage basins), with remaining samples separated into larger clades from the Mojave desert, and western populations from the California Floristic Province of California and northern Baja California. -
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). -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
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 -
70.1, 5 September 2008 ISSN 1944-8120
PECKHAMIA 70.1, 5 September 2008 ISSN 1944-8120 This is a PDF version of PECKHAMIA 3(2): 27-60, December 1995. Pagination of the original document has been retained. PECKHAMIA Volume 3 Number 2 Publication of the Peckham Society, an informal organization dedicated to research in the biology of jumping spiders. CONTENTS ARTICLES: A LIST OF THE JUMPING SPIDERS (SALTICIDAE) OF THE ISLANDS OF THE CARIBBEAN REGION G. B. Edwards and Robert J. Wolff..........................................................................27 DECEMBER 1995 A LIST OF THE JUMPING SPIDERS (SALTICIDAE) OF THE ISLANDS OF THE CARIBBEAN REGION G. B. Edwards Florida State Collection of Arthropods Division of Plant Industry P. O. Box 147100 Gainesville, FL 32614-7100 USA Robert J. Wolff1 Biology Department Trinity Christian College 6601 West College Drive Palos Heights, IL 60463 USA The following is a list of the jumping spiders that have been reported from the Caribbean region. We have interpreted this in a broad sense, so that all islands from Trinidad to the Bahamas have been included. Furthermore, we have included Bermuda, even though it is well north of the Caribbean region proper, as a more logical extension of the island fauna rather than the continental North American fauna. This was mentioned by Banks (1902b) nearly a century ago. Country or region (e. g., pantropical) records are included for those species which have broader ranges than the Caribbean area. We have not specifically included the islands of the Florida Keys, even though these could legitimately be included in the Caribbean region, because the known fauna is mostly continental. However, when Florida is known as the only continental U.S.A. -
A LIST of the JUMPING SPIDERS of MEXICO. David B. Richman and Bruce Cutler
PECKHAMIA 62.1, 11 October 2008 ISSN 1944-8120 This is a PDF version of PECKHAMIA 2(5): 63-88, December 1988. Pagination of the original document has been retained. 63 A LIST OF THE JUMPING SPIDERS OF MEXICO. David B. Richman and Bruce Cutler The salticids of Mexico are poorly known. Only a few works, such as F. O. Pickard-Cambridge (1901), have dealt with the fauna in any depth and these are considerably out of date. Hoffman (1976) included jumping spiders in her list of the spiders of Mexico, but the list does not contain many species known to occur in Mexico and has some synonyms listed. It is our hope to present a more complete list of Mexican salticids. Without a doubt such a work is preliminary and as more species are examined using modern methods a more complete picture of this varied fauna will emerge. The total of 200 species indicates more a lack of study than a sparse fauna. We would be surprised if the salticid fauna of Chiapas, for example, was not larger than for all of the United States. Unfortunately, much of the tropical forest may disappear before this fauna is fully known. The following list follows the general format of our earlier (1978) work on the salticid fauna of the United States and Canada. We have not prepared a key to genera, at least in part because of the obvious incompleteness of the list. We hope, however, that this list will stimulate further work on the Mexican salticid fauna. Acragas Simon 1900: 37. -
SOME SPIDERS from NORTHERN LOUISIANA. by NATHAN BANKS
188 ENTOMOLOGICAL SOCIETY misnomer. Mr. Pratt remarked that the collectors for Messrs. Godman and Salvin had no time to study habits, since they were told simply to collect as much material as possible. Mr. Banks presented the following paper : SOME SPIDERS FROM NORTHERN LOUISIANA. By NATHAN BANKS. During the summer of 1891 I gathered a small collection of spiders from the vicinity of Shreveport, Louisiana. Although there are few peculiar or strange species in the collection, still it is of some interest, as so little is at present known of the distribu tion of our spiders. Yet there are several uncommon species, at least uncommon to one acquainted chiefly with more northern forms. Such are the Prodidomus rufus, Tetragonophthalma dubia, Acartauchcnius texana, and Thargalia aurata. Two species quite rare in the North are Histiagonia rostrata and Ballus youngi. About 127 species are recorded in this list, distributed in twenty-one families. The collection is representative of the southern Mississippi Valley fauna. This differs from the South Atlantic fauna in having some southwestern species. Seven to be nsw and are here described a species appear ; few others, principally in the Lycosidse, may prove to be new when the southern forms of this family are better known. THERAPHOSID^E. DRASSID^E. Eurypelma hentzi Girard. Gnaphosa sericata Koch. Drassns bicolor Htz. SCYTODID^:. Cesonia bilineata Htz. Loxosceles rufipes Duf. Prosthesima depressa Em. FlLISTATIDyE. Prosthesima atra Htz. Filistata hibernalis Hentz. Megamyrmecion lepidium n. sp. DYSDERID^E. CLUBIONID^E. Ariadne bicolor Hentz. Clubiona obesa Hentz. Clubiona abboti Koch. Chiracanthium inclusa Hentz. Thalamia Hentz. parietalis Anyphaena gracilis Hentz. -
WO 2017/035099 Al 2 March 2017 (02.03.2017) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/035099 Al 2 March 2017 (02.03.2017) P O P C T (51) International Patent Classification: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, C07C 39/00 (2006.01) C07D 303/32 (2006.01) DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, C07C 49/242 (2006.01) HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, (21) International Application Number: MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PCT/US20 16/048092 PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (22) International Filing Date: SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, 22 August 2016 (22.08.2016) TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (25) Filing Language: English (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (26) Publication Language: English GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, (30) Priority Data: TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, 62/208,662 22 August 2015 (22.08.2015) US TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (71) Applicant: NEOZYME INTERNATIONAL, INC.