(ARANEAE: SALTICIDAE)* by WAYNE MADDISON Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts 02138
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Oak Woodland Litter Spiders James Steffen Chicago Botanic Garden
Oak Woodland Litter Spiders James Steffen Chicago Botanic Garden George Retseck Objectives • Learn about Spiders as Animals • Learn to recognize common spiders to family • Learn about spider ecology • Learn to Collect and Preserve Spiders Kingdom - Animalia Phylum - Arthropoda Subphyla - Mandibulata Chelicerata Class - Arachnida Orders - Acari Opiliones Pseudoscorpiones Araneae Spiders Arachnids of Illinois • Order Acari: Mites and Ticks • Order Opiliones: Harvestmen • Order Pseudoscorpiones: Pseudoscorpions • Order Araneae: Spiders! Acari - Soil Mites Characteriscs of Spiders • Usually four pairs of simple eyes although some species may have less • Six pair of appendages: one pair of fangs (instead of mandibles), one pair of pedipalps, and four pair of walking legs • Spinnerets at the end of the abdomen, which are used for spinning silk threads for a variety of purposes, such as the construction of webs, snares, and retreats in which to live or to wrap prey • 1 pair of sensory palps (often much larger in males) between the first pair of legs and the chelicerae used for sperm transfer, prey manipulation, and detection of smells and vibrations • 1 to 2 pairs of book-lungs on the underside of abdomen • Primitively, 2 body regions: Cephalothorax, Abdomen Spider Life Cycle • Eggs in batches (egg sacs) • Hatch inside the egg sac • molt to spiderlings which leave from the egg sac • grows during several more molts (instars) • at final molt, becomes adult – Some long-lived mygalomorphs (tarantulas) molt after adulthood Phenology • Most temperate -
Spiders (Araneae) of the Abandoned Pasture Near the Village of Malé Kršteňany (Western Slovakia)
Annales Universitatis Paedagogicae Cracoviensis Studia Naturae, 2: 39–56, 2017, ISSN 2543-8832 DOI: 10.24917/25438832.2.3 Valerián Franc*, Michal Fašanga Department of Biology and Ecology, Faculty of Natural Sciences, Matej Bel University, Tajovského 40, 97401 Banská Bystrica, *[email protected] Spiders (Araneae) of the abandoned pasture near the village of Malé Kršteňany (Western Slovakia) Introduction Our research site is located on the SE slope of the hill of Drieňový vrch (cadaster of the village of Malé Kršteňany). It is the southernmost edge of the Strážovské vrchy Mountains (Mts) (48°55ʹ46ʹʹN; 18°26ʹ05ʹʹE), separated from the central massif by the river ow Nitrica. is area is considerably inuenced by human activity: In the past, it had massive deforestation and agricultural use (mainly as pasture), recently, it is dominated by mining activities (several quarries). e whole area is out of the territo- rial protection, with the exception of the little Nature reserve Veľký vrch, surrounded by two quarries, and the le one is more or less abandoned. In the past, this area was used mainly for grazing, but this is currently very limited. Our research site is an aban- doned pasture; therefore, ecological succession is carried out intensively here. Forgot- ten aer-utility areas (abandoned quarries, pastures, industrial sites) are usually con- sidered to be ‘sterile’ and unattractive for zoological research, but this may not always correspond to reality. Even in our research site, we have carried out several rare and surprising ndings. We would like to present the results of our research in this paper. It is sad, but a large amount of abandoned pastures is scattered throughout Slova- kia. -
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. -
REVISION of the JUMPING SPIDERS of the GENUS PHIDIPPUS (ARANEAE: SALTICIDAE) by G
Occasional Papers of the Florida State Collection of Arthropods Volume 11 2004 REVISION OF THE JUMPING SPIDERS OF THE GENUS PHIDIPPUS (ARANEAE: SALTICIDAE) by G. B. Edwards Florida Department of Agriculture and Consumer Services Charles H. Bronson, Commissioner 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Occasional Papers of the Florida State Collection of Arthropods Volume 11 REVISION OF THE JUMPING SPIDERS OF THE GENUS PHIDIPPUS (ARANEAE: SALTICIDAE) by G. B. EDWARDS Curator: Arachnida & Myriapoda Florida State Collection of Arthropods FDACS, Division of Plant Industry Bureau of Entomology, Nematology, and Plant Pathology P. O. Box 147100, 1911 SW 34th Street Gainesville, Florida 32614-7100 USA 2004 FLORIDA DEPARTMENT OF AGRICULTURE AND CONSUMER SERVICES DIVISION OF PLANT INDUSTRY and THE CENTER FOR SYSTEMATIC ENTOMOLOGY Gainesville, Florida FLORIDA DEPARTMENT OF AGRICULTURE AND CONSUMER SERVICES Charles H. Bronson, Commissioner . Tallahassee Terry L. Rhodes, Assistant Commissioner . Tallahassee Craig Meyer, Deputy Commissioner . Tallahassee Richard D. Gaskalla, Director, Division of Plant Industry (DPI) . Gainesville Connie C. Riherd, Assistant Director, Division of Plant Industry . Gainesville Wayne N. Dixon, Ph.D., Bureau Chief, Entomology, Nematology and Plant Pathology . Gainesville Don L. Harris, Bureau Chief, Methods Development and Biological Control . Gainesville Richard A. Clark, Bureau Chief, Plant and Apiary Inspection . Gainesville Gregory Carlton, Bureau Chief, Pest Eradication and Control . Winter Haven Michael C. Kesinger, Bureau Chief, Budwood Registration . Winter Haven CENTER FOR SYSTEMATIC ENTOMOLOGY BOARD OF DIRECTORS G. B. Edwards, Ph.D., President . DPI, Gainesville Paul E. Skelley, Ph.D., Vice-President . DPI, Gainesville Gary J. Steck, Ph.D., Secretary . -
How Jumping Spiders (Araneae: Salticidae) Find and Use Indirect Routes to Reach Their Sighted Objectives
Peckhamia 184.1 How jumping spiders use indirect routes 1 PECKHAMIA 184.1, 10 May 2019, 1―13 ISSN 2161―8526 (print) urn:lsid:zoobank.org:pub:1987105E-0056-4FCD-87EF-C29F74073AB9 (registered 08 MAY 2019) ISSN 1944―8120 (online) How jumping spiders (Araneae: Salticidae) find and use indirect routes to reach their sighted objectives David E. Hill 1 1 213 Wild Horse Creek Drive, Simpsonville SC 29680, USA, email [email protected] Abstract. Jumping spiders (Salticidae) are not limited to planning their route at the onset of pursuit, but dynamically collect and use new information as they complete an indirect route or detour. There is strong support for the hypothesis that selection of the immediate route is based on the presence of a visible connection leading to the objective. In turn salticids can use these visible connections as secondary (or intermediate) objectives. Salticids can compute the expected direction and distance of their primary objective after they move to a new location, and frequently turn (reorient) to face their original objective to begin a new segment of pursuit. Completion of a sequence of these pursuit segments allows the salticid to successfully complete a complicated and indirect route of pursuit even when this is not visible at the onset. Key words. Anasaitis, cognition, Colonus, detour, direction information, distance information, gravity information, Habronattus, Hentzia, landmarks, Lyssomanes, Maevia, map direction, orientation, Phidippus, Platycryptus, Portia, reorientation, route selection, secondary objectives, segmented pursuit, Spartaeinae, spatial integration, visual cues The ability of salticid spiders to complete detoured or indirect pursuits of visual objectives has been known for some time (e.g., Bilsing 1920; Heil 1936; Hill 1977, 2008, 2018a; Jackson & Wilcox 1993). -
Acquired Natural Enemies of Oxyops Vitiosa 1
Christensen et al.: Acquired Natural Enemies of Oxyops vitiosa 1 ACQUIRED NATURAL ENEMIES OF THE WEED BIOLOGICAL CONTROL AGENT OXYOPS VITIOSA (COLEPOTERA: CURCULIONIDAE) ROBIN M. CHRISTENSEN, PAUL D. PRATT, SHERYL L. COSTELLO, MIN B. RAYAMAJHI AND TED D. CENTER USDA/ARS, Invasive Plant Research Laboratory, 3225 College Ave., Ft. Lauderdale, FL 33314 ABSTRACT The Australian curculionid Oxyops vitiosa Pascoe was introduced into Florida in 1997 as a biological control agent of the invasive tree Melaleuca quinquenervia (Cav.) S. T. Blake. Pop- ulations of the weevil increased rapidly and became widely distributed throughout much of the invasive tree’s adventive distribution. In this study we ask if O. vitiosa has acquired nat- ural enemies in Florida, how these enemies circumvent the protective terpenoid laden exu- dates on larvae, and what influence 1 of the most common natural enemies has on O. vitiosa population densities? Surveys of O. vitiosa populations and rearing of field-collected individ- uals resulted in no instances of parasitoids or pathogens exploiting weevil eggs or larvae. In contrast, 44 species of predatory arthropods were commonly associated (>5 individuals when pooled across all sites and sample dates) with O. vitiosa. Eleven predatory species were ob- served feeding on O. vitiosa during timed surveys, including 6 pentatomid species, 2 formi- cids and 3 arachnids. Species with mandibulate or chelicerate mouthparts fed on adult stages whereas pentatomids, with haustellate beaks, pierced larval exoskeletons thereby by- passing the protective larval coating. Observations of predation were rare, with only 8% of timed surveys resulting in 1 or more instances of attack. Feeding by the pentatomid Podisus mucronatus Uhler accounted for 76% of all recorded predation events. -
1 the RESTRUCTURING of ARTHROPOD TROPHIC RELATIONSHIPS in RESPONSE to PLANT INVASION by Adam B. Mitchell a Dissertation Submitt
THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell 1 A dissertation submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology and Wildlife Ecology Winter 2019 © Adam B. Mitchell All Rights Reserved THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell Approved: ______________________________________________________ Jacob L. Bowman, Ph.D. Chair of the Department of Entomology and Wildlife Ecology Approved: ______________________________________________________ Mark W. Rieger, Ph.D. Dean of the College of Agriculture and Natural Resources Approved: ______________________________________________________ Douglas J. Doren, Ph.D. Interim Vice Provost for Graduate and Professional Education I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Douglas W. Tallamy, Ph.D. Professor in charge of dissertation I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Charles R. Bartlett, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Jeffery J. Buler, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. -
A Revision of the Genus Hentzia (Araneae, Salticidae)
Richman, D . A . 1989 . A revision of Hentzia (Araneae, Salticidae) . J . Arachnol., 17 :285-344 . A REVISION OF THE GENUS HENTZIA (ARANEAE, SALTICIDAE) David B . Richman Department of Entomology, Plant Pathology and Weed Science New Mexico State University Las Cruces, New Mexico 88003 USA ABSTRACT The genus Hentzia belongs in the subfamily Dendryphantinae of the family Salticidae . It appears to be closely related to "Beata" wickhami and the genus Anicius . Twenty species are recognized in this revision, occurring from Nova Scotia and Quebec in the north to northern South America in the south . The genus ranges along the coastal areas of Mexico on both sides of the continent north to Arizona in the west and through central Texas to Minnesota . Six new species are described . These are H. calypso from Jamaica, H. chekika from Florida, the Bahamas and Cuba, H. cubana from Cuba, H. pima from Arizona, H. whitcombi from Guadeloupe, Puerto Rico and a few other Caribbean islands, and H. zombia from Hispaniola . The genera Parahentzia Bryant 1943, and Maeviobeata Caporiacco 1947, are here made junior synonyms of Hentzia . Parahentzia insignita Chickering 1946, is made a junior synonym of Anoka parallela Peckham and Peckham 1894 . Anoka peckhami Cockerell 1893, and Wala albovittata Keyserling 1885, become junior synonyms of Icius vittatus Keyserling 1885 . All of these are placed in the genus Hentzia . Balmaceda peckhami Bryant 1940 is found to be the female of H. tibialis Bryant 1940 . The female paratype of Hentzia tibialis Bryant 1940, is found to be the female of Hentzia chekika n . sp . Finally Wala noda Chamberlin 1916, is transferred from Hentzia to Corythalia . -
Plant Nectar Contributes to the Survival, Activity, Growth
PLANT NECTAR CONTRIBUTES TO THE SURVIVAL, ACTIVITY, GROWTH, AND FECUNDITY OF THE NECTAR-FEEDING WANDERING SPIDER CHEIRACANTHIUM INCLUSUM (HENTZ) (ARANEAE: MITURGIDAE) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Robin M. Taylor, B.A, M.A. ***** The Ohio State University 2004 Dissertation Committee: Approved by Dr. Richard A. Bradley, Advisor Dr. Thomas E. Hetherington _____________________________ Dr. W. Mitch Masters Advisor Department of Evolution, Ecology, and Organismal Biology ABSTRACT Spiders are valued for their predation of insect pests, and, evaluated as an “assemblage” of species that employ different predatory strategies, constitute a natural biological control, particularly in agricultural crops. Spiders are obligate carnivores, requiring prey for normal growth, development, and reproduction. Because biologists have worked under the assumption that spiders are exclusively carnivorous, studies of the ecology of spiders and their acquisition and allocation of energy have assumed that prey is the single object of any spider’s foraging. The discovery in 1984 that orb-weaving spiderlings benefited nutritionally from pollen grains incidentally trapped by their webs, which they eat and recycle, was noteworthy. Growing evidence indicates that a large group of spiders may routinely exploit another plant-based food source: plant nectar. Observations of nectar feeding have been reported among crab spiders (Thomisidae), jumping spiders (Salticidae), and running spiders (Anyphaenidae, Clubionidae, and Corinnidae), all non-webbuilding wanderers that occupy vegetation. Spiders have the capacity to detect and digest plant nectar, and spiders that wander in vegetation are able to encounter nectar. Lab experiments show that newly-emerged, prey-deprived spiders live longer if they are provided with sucrose, a nectar proxy. -
THESIS a SURVEY of the ARTHROPOD FAUNA ASSOCIATED with HEMP (CANNABIS SATIVA L.) GROWN in EASTERN COLORADO Submitted by Melissa
THESIS A SURVEY OF THE ARTHROPOD FAUNA ASSOCIATED WITH HEMP (CANNABIS SATIVA L.) GROWN IN EASTERN COLORADO Submitted by Melissa Schreiner Department of Bioagricultural Sciences and Pest Management In partial fulfillment of the requirements For the Degree of Master of Science Colorado State University Fort Collins, Colorado Fall 2019 Master’s Committee: Advisor: Whitney Cranshaw Frank Peairs Mark Uchanski Copyright by Melissa Schreiner 2019 All Rights Reserved ABSTRACT A SURVEY OF THE ARTHROPOD FAUNA ASSOCIATED WITH HEMP (CANNABIS SATIVA L.) GROWN IN EASTERN COLORADO Industrial hemp was found to support a diverse complex of arthropods in the surveys of hemp fields in eastern Colorado. Seventy-three families of arthropods were collected from hemp grown in eight counties in Colorado in 2016, 2017, and 2018. Other important groups found in collections were of the order Diptera, Coleoptera, and Hemiptera. The arthropods present in fields had a range of association with the crop and included herbivores, natural enemies, pollen feeders, and incidental species. Hemp cultivars grown for seed and fiber had higher insect species richness compared to hemp grown for cannabidiol (CBD). This observational field survey of hemp serves as the first checklist of arthropods associated with the crop in eastern Colorado. Emerging key pests of the crop that are described include: corn earworm (Helicoverpa zea (Boddie)), hemp russet mite (Aculops cannibicola (Farkas)), cannabis aphid (Phorodon cannabis (Passerini)), and Eurasian hemp borer (Grapholita delineana (Walker)). Local outbreaks of several species of grasshoppers were observed and produced significant crop injury, particularly twostriped grasshopper (Melanoplus bivittatus (Say)). Approximately half (46%) of the arthropods collected in sweep net samples during the three year sampling period were categorized as predators, natural enemies of arthropods. -
List of Ohio Spiders
List of Ohio Spiders 20 March 2018 Richard A. Bradley Department of EEO Biology Ohio State University Museum of Biodiversity 1315 Kinnear Road Columbus, OH 43212 This list is based on published specimen records of spider species from Ohio. Additional species that have been recorded during the Ohio Spider Survey (beginning 1994) are also included. I would very much appreciate any corrections; please mail them to the above address or email ([email protected]). 656 [+5] Species Mygalomorphae Antrodiaetidae (foldingdoor spiders) (2) Antrodiaetus robustus (Simon, 1890) Antrodiaetus unicolor (Hentz, 1842) Atypidae (purseweb spiders) (3) Sphodros coylei Gertsch & Platnick, 1980 Sphodros niger (Hentz, 1842) Sphodros rufipes (Latreille, 1829) Ctenizidae (trapdoor spiders) (1) Ummidia audouini (Lucas, 1835) Araneomorphae Agelenidae (funnel weavers) (14) Agelenopsis emertoni Chamberlin & Ivie, 1935 | Agelenopsis kastoni Chamberlin & Ivie, 1941 | Agelenopsis naevia (Walckenaer, 1805) grass spiders Agelenopsis pennsylvanica (C.L. Koch, 1843) | Agelnopsis potteri (Blackwell, 1846) | Agelenopsis utahana (Chamberlin & Ivie, 1933) | Coras aerialis Muma, 1946 Coras juvenilis (Keyserling, 1881) Coras lamellosus (Keyserling, 1887) Coras medicinalis (Hentz, 1821) Coras montanus (Emerton, 1889) Tegenaria domestica (Clerck, 1757) barn funnel weaver In Wadotes calcaratus (Keyserling, 1887) Wadotes hybridus (Emerton, 1889) Amaurobiidae (hackledmesh weavers) (2) Amaurobius ferox (Walckenaer, 1830) In Callobius bennetti (Blackwall, 1848) Anyphaenidae (ghost spiders) -
(Arachnida: Araneae) Along an Outdoor – Indoor Habitat Gradient: Preliminary Findings from Piedmont Virginia
Virginia Journal of Science Note: This manuscript has been accepted for publication and is online Volume 70, Issue 3 ahead of print. It will undergo copyediting, typesetting, and review of the Fall 2019 resulting proof before it is published in its final form. doi: 10.25778/ej65-br87 The Diversity and Distribution of Spiders (Arachnida: Araneae) Along an Outdoor – Indoor Habitat Gradient: Preliminary Findings from Piedmont Virginia William Kish and Sujan Henkanaththegedara1 Longwood University ABSTRACT Although the United States supports a considerable diversity of spiders, some aspects of spider habitat use and niche specialization are poorly documented. Specifically, little attention has been given to explore how urban development affects the diversity and abundance of arthropods. We sampled spiders along an outdoor – indoor habitat gradient at Longwood University to understand the impact of urbanization on species diversity and abundance. We found 50 taxa of spiders belonging to 43 genera and 16 families. Overall, the most abundant spider family across three sampling sites was Araneidae (orb-weavers; 18.2%) followed by Lycosidae (wolf spiders; 14.8%), Salticidae (jumping spiders; 13.6%) and Linyphiidae (sheetweb spiders; 12.5%). We found the highest species richness, spider abundance, and Shannon-Wiener diversity from Lancer Park (i.e. outdoors habitat), followed by the habitats associated with outside of the science center building (i.e. marginal habitat) and the lowest spider diversity inside the science building (i.e. indoors habitat). We also found a strong positive correlation between overall spider diversity and air temperature for outdoors and marginal habitats, but no correlation with relative humidity. Our study adds original knowledge about habitat use of spiders along an outdoor - indoor habitat gradient and arthropod use of indoor biome.