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(Opiliones: Monoscutidae) – the Genus Pantopsalis
Tuhinga 15: 53–76 Copyright © Te Papa Museum of New Zealand (2004) New Zealand harvestmen of the subfamily Megalopsalidinae (Opiliones: Monoscutidae) – the genus Pantopsalis Christopher K. Taylor Department of Molecular Medicine and Physiology, University of Auckland, Private Bag 92019, Auckland, New Zealand ([email protected]) ABSTRACT: The genus Pantopsalis Simon, 1879 and its constituent species are redescribed. A number of species of Pantopsalis show polymorphism in the males, with one form possessing long, slender chelicerae, and the other shorter, stouter chelicerae. These forms have been mistaken in the past for separate species. A new species, Pantopsalis phocator, is described from Codfish Island. Megalopsalis luna Forster, 1944 is transferred to Pantopsalis. Pantopsalis distincta Forster, 1964, P. wattsi Hogg, 1920, and P. grayi Hogg, 1920 are transferred to Megalopsalis Roewer, 1923. Pantopsalis nigripalpis nigripalpis Pocock, 1902, P. nigripalpis spiculosa Pocock, 1902, and P. jenningsi Pocock, 1903 are synonymised with P. albipalpis Pocock, 1902. Pantopsalis trippi Pocock, 1903 is synonymised with P. coronata Pocock, 1903, and P. mila Forster, 1964 is synonymised with P. johnsi Forster, 1964. A list of species described to date from New Zealand and Australia in the Megalopsalidinae is given as an appendix. KEYWORDS: taxonomy, Arachnida, Opiliones, male polymorphism, sexual dimorphism. examines the former genus, which is endemic to New Introduction Zealand. The more diverse Megalopsalis will be dealt with Harvestmen (Opiliones) are abundant throughout New in another publication. All Pantopsalis species described to Zealand, being represented by members of three different date are reviewed, and a new species is described. suborders: Cyphophthalmi (mite-like harvestmen); Species of Monoscutidae are found in native forest the Laniatores (short-legged harvestmen); and Eupnoi (long- length of the country, from the Three Kings Islands in the legged harvestmen; Forster & Forster 1999). -
A Review of the Anti-Predator Devices of Spiders* Invaders Away Or Kill and Eat Them
Bull. Br. arachnol. Soc. (1995) 10 (3), 81-96 81 A review of the anti-predator devices of spiders* invaders away or kill and eat them. The pirate spiders (Mimetidae) that have been studied feed almost J. L. Cloudsley-Thompson exclusively on other spiders, whilst certain Salticidae 10 Battishill Street, (Portia spp.) feed not only upon insects, but sometimes London Nl 1TE also on other jumping spiders, and even tackle large orb-weavers in their webs (see below). Several other Summary families and genera, including Archaeidae, Palpimanus (Palpimanidae), Argyrodes and Theridion (Theridiidae), The predators of spiders are mostly either about the and Chorizopes (Araneidae) contain species that include same size as their prey (arthropods) or much larger (vertebrates), against each of which different types of de- other spiders in their diet. Sexual cannibalism has been fence have evolved. Primary defences include anachoresis, reviewed by Elgar (1992). Other books in which the phenology, crypsis, protective resemblance and disguise, enemies of spiders are discussed include: Berland (1932), spines and warning coloration, mimicry (especially of ants), Bristowe (1958), Cloudsley-Thompson (1958, 1980), cocoons and retreats, barrier webs, web stabilimenta and Edmunds (1974), Gertsch (1949), Main (1976), Millot detritus, and communal webs. Secondary defences are flight, dropping to the ground, colour change and thanatosis, (1949), Preston-Mafham, R. & K. (1984), Savory (1928), web vibration, whirling and bouncing, autotomy, venoms Thomas (1953) and Wise (1993). (For earlier references, and defensive fluids, urticating setae, warning sounds and see Warburton, 1909). deimatic displays. The anti-predator adaptations of spiders The major predators of spiders fall into two cate- are extremely complex, and combinations of the devices gories: (a) those about the same size as their prey (mainly listed frequently occur. -
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. -
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 . -
Taxonomic Revision and Phylogenetic Hypothesis for the Jumping Spider Subfamily Ballinae (Araneae, Salticidae)
UC Berkeley UC Berkeley Previously Published Works Title Taxonomic revision and phylogenetic hypothesis for the jumping spider subfamily Ballinae (Araneae, Salticidae) Permalink https://escholarship.org/uc/item/5x19n4mz Journal Zoological Journal of the Linnean Society, 142(1) ISSN 0024-4082 Author Benjamin, S P Publication Date 2004-09-01 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Blackwell Science, LtdOxford, UKZOJZoological Journal of the Linnean Society0024-4082The Lin- nean Society of London, 2004? 2004 1421 182 Original Article S. P. BENJAMINTAXONOMY AND PHYLOGENY OF BALLINAE Zoological Journal of the Linnean Society, 2004, 142, 1–82. With 69 figures Taxonomic revision and phylogenetic hypothesis for the jumping spider subfamily Ballinae (Araneae, Salticidae) SURESH P. BENJAMIN* Department of Integrative Biology, Section of Conservation Biology (NLU), University of Basel, St. Johanns-Vorstadt 10, CH-4056 Basel, Switzerland Received July 2003; accepted for publication February 2004 The subfamily Ballinae is revised. To test its monophyly, 41 morphological characters, including the first phyloge- netic use of scale morphology in Salticidae, were scored for 16 taxa (1 outgroup and 15 ingroup). Parsimony analysis of these data supports monophyly based on five unambiguous synapomorphies. The paper provides new diagnoses, descriptions of new genera, species, and a key to the genera. At present, Ballinae comprises 13 nominal genera, three of them new: Afromarengo, Ballus, Colaxes, Cynapes, Indomarengo, Leikung, Marengo, Philates and Sadies. Copocrossa, Mantisatta, Pachyballus and Padilla are tentatively included in the subfamily. Nine new species are described and illustrated: Colaxes horton, C. wanlessi, Philates szutsi, P. thaleri, P. zschokkei, Indomarengo chandra, I. -
Full Program (.PDF)
48th Annual Meeting of the American Arachnological Society 16-20 June 2019 Lexington, Virginia Table of Contents Acknowledgements ............................................................................................................ 1 Venue and Town ................................................................................................................. 1 Emergency Contacts .......................................................................................................... 2 American Arachnological Society Code of Professional Conduct ............................. 3 MEETING SCHEDULE IN BRIEF ....................................................................................... 4 MEETING SCHEDULE ........................................................................................................ 6 POSTER TITLES AND AUTHORS ................................................................................... 15 ABSTRACTS ...................................................................................................................... 18 ORAL PRESENTATION ABSTRACTS ..................................................................................... 19 POSTER ABSTRACTS ............................................................................................................... 47 CONFERENCE PARTICIPANTS ...................................................................................... 63 Acknowledgements This meeting was made possible by the enthusiastic support of numerous people. We are especially grateful -
Abstract Book
ABSTRACT BOOK Canterbury, New Zealand 10–15 February 2019 21st International Congress of Arachnology ORGANISING COMMITTEE MAIN ORGANISERS Cor Vink Peter Michalik Curator of Natural History Curator of the Zoological Museum Canterbury Museum University of Greifswald Rolleston Avenue, Christchurch Loitzer Str 26, Greifswald New Zealand Germany LOCAL ORGANISING COMMITTEE Ximena Nelson (University of Canterbury) Adrian Paterson (Lincoln University) Simon Pollard (University of Canterbury) Phil Sirvid (Museum of New Zealand, Te Papa Tongarewa) Victoria Smith (Canterbury Museum) SCIENTIFIC COMMITTEE Anita Aisenberg (IICBE, Uruguay) Miquel Arnedo (University of Barcelona, Spain) Mark Harvey (Western Australian Museum, Australia) Mariella Herberstein (Macquarie University, Australia) Greg Holwell (University of Auckland, New Zealand) Marco Isaia (University of Torino, Italy) Lizzy Lowe (Macquarie University, Australia) Anne Wignall (Massey University, New Zealand) Jonas Wolff (Macquarie University, Australia) 21st International Congress of Arachnology 1 INVITED SPEAKERS Plenary talk, day 1 Sensory systems, learning, and communication – insights from amblypygids to humans Eileen Hebets University of Nebraska-Lincoln, Nebraska, USA E-mail: [email protected] Arachnids encompass tremendous diversity with respect to their morphologies, their sensory systems, their lifestyles, their habitats, their mating rituals, and their interactions with both conspecifics and heterospecifics. As such, this group of often-enigmatic arthropods offers unlimited and sometimes unparalleled opportunities to address fundamental questions in ecology, evolution, physiology, neurobiology, and behaviour (among others). Amblypygids (Order Amblypygi), for example, possess distinctly elongated walking legs covered with sensory hairs capable of detecting both airborne and substrate-borne chemical stimuli, as well as mechanoreceptive information. Simultaneously, they display an extraordinary central nervous system with distinctly large and convoluted higher order processing centres called mushroom bodies. -
Multiple Exaggerated Weapon Morphs: a Novel Form of Male Polymorphism in Harvestmen Received: 22 July 2015 † Accepted: 12 October 2015 Christina J
www.nature.com/scientificreports OPEN Multiple exaggerated weapon morphs: a novel form of male polymorphism in harvestmen Received: 22 July 2015 † Accepted: 12 October 2015 Christina J. Painting , Anna F. Probert, Daniel J. Townsend & Gregory I. Holwell Published: 06 November 2015 Alternative reproductive tactics in animals are commonly associated with distinct male phenotypes resulting in polymorphism of sexually selected weapons such as horns and spines. Typically, morphs are divided between small (unarmed) and large (armed) males according to one or more developmental thresholds in association with body size. Here, we describe remarkable weapon trimorphism within a single species, where two exaggerated weapon morphs and a third morph with reduced weaponry are present. Male Pantopsalis cheliferoides harvestmen display exaggerated chelicerae (jaws) which are highly variable in length among individuals. Across the same body size spectrum, however, some males belong to a distinct second exaggerated morph which possesses short, broad chelicerae. Multiple weapon morphs in a single species is a previously unknown phenomenon and our findings have significant implications for understanding weapon diversity and maintenance of polymorphism. Specifically, this species will be a valuable model for testing how weapons diverge by being able to test directly for the circumstances under which a certain weapon type is favoured and how weapon shape relates to performance. Sexual selection has driven the evolution of a spectacular array of male weaponry and alternative repro- ductive tactics (ARTs) among animals1,2. Although the profusion of weaponry can be explained by the increased mating opportunities they confer, these benefits do not necessarily explain why there is such an incredible diversity in the form and function of weapons among species. -
A Molecular Phylogenetic Approach to the New Zealand Species of Enantiobuninae (Opiliones : Eupnoi : Neopilionidae)
A molecular phylogenetic approach to the New Zealand species of Enantiobuninae (Opiliones : Eupnoi : Neopilionidae) The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Vélez, Sebastián, Rosa Fernández, and Gonzalo Giribet. 2014. “A Molecular Phylogenetic Approach to the New Zealand Species of Enantiobuninae (Opiliones#: Eupnoi#: Neopilionidae).” Invertebrate Systematics 28, no. 6: 565-589. doi:10.1071/IS14030 Published Version doi:10.1071/IS14030 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:14425988 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Open Access Policy Articles, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#OAP Page 1 of 61 Invertebrate Systematics 1 A molecular phylogenetic approach to the New Zealand species of Enantiobuninae 2 (Opiliones : Eupnoi : Neopilionidae) 3 4 Sebastián VélezA,B,C, Rosa FernándezA, and Gonzalo GiribetA 5 6 AMuseum of Comparative Zoology, Department of Organismic and Evolutionary 7 Biology, HarvardFor University, Review 26 Oxford Street, Cambridge,Only MA 02138, USA. 8 BCurrent address: Biology Department, Worcester State University, 486 Chandler Street, 9 Worcester, MA 01602, USA. 10 CCorresponding author. Email:[email protected] 11 12 Running title: Phylogenetics of the New Zealand Enantiobuninae 1 http://www.publish.csiro.au/journals/is Invertebrate Systematics Page 2 of 61 13 Abstract. We report the first phylogeny based on molecular data for the New 14 Zealand species in the genera Forsteropsalis, Pantopsalis, and Mangatangi, and 15 comment on the taxonomic implications of our results, including the diagnostic viability 16 of important morphological characters. -
Sexual Dimorphism in the Arachnid Orders
Sexual dimorphism in the Arachnid orders Callum J. McLean1, Russell J. Garwood2,3 and Charlotte A. Brassey1 1 School of Science and the Environment, Manchester Metropolitan University, Manchester, UK 2 School of Earth and Environmental Sciences, University of Manchester, Manchester, UK 3 Earth Sciences Department, Natural History Museum, London, UK ABSTRACT Sexual differences in size and shape are common across the animal kingdom. The study of sexual dimorphism (SD) can provide insight into the sexual- and natural-selection pressures experienced by males and females in different species. Arachnids are diverse, comprising over 100,000 species, and exhibit some of the more extreme forms of SD in the animal kingdom, with the males and females of some species differing dramatically in body shape and/or size. Despite this, research on arachnid SD has primarily focused on specific clades as opposed to observing traits across arachnid orders, the smallest of which have received comparatively little attention. This review provides an overview of the research to date on the trends and potential evolutionary drivers for SD and sexual size dimorphism (SSD) in individual arachnid orders, and across arachnids as a whole. The most common trends across Arachnida are female-biased SSD in total body size, male-biased SSD in relative leg length and SD in pedipalp length and shape. However, the evolution of sexually dimorphic traits within the group is difficult to elucidate due to uncertainty in arachnid phylogenetic relationships. Based on the dataset we have gathered here, we highlight gaps in our current understanding and suggest areas for future research. Subjects Animal Behavior, Entomology, Evolutionary Studies, Zoology Keywords Arachnid, Sexual dimorphism, Sexual selection, Rensch’s rule Submitted 19 March 2018 Accepted 14 September 2018 INTRODUCTION Published 6 November 2018 Sexual dimorphism (SD), the difference in morphological, physiological and behavioural Corresponding author traits between males and females, is ubiquitous in nature. -
Color and Communication in Habronattus Jumping Spiders
Color and Communication in Habronattus Jumping Spiders: Tests of Sexual and Ecological Selection by Lisa Anne Taylor A Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy Approved January 2012 by the Graduate Supervisory Committee: Kevin McGraw, Chair Ronald Rutowski David Clark James Johnson John Alcock ARIZONA STATE UNIVERSITY May 2012 ABSTRACT Differences between males and females can evolve through a variety of mechanisms, including sexual and ecological selection. Because coloration is evolutionarily labile, sexually dichromatic species are good models for understanding the evolution of sex differences. While many jumping spiders exhibit diverse and brilliant coloration, they have been notably absent from such studies. In the genus Habronattus, females are drab and cryptic while males are brilliantly colored, displaying some of these colors to females during elaborate courtship dances. Here I test multiple hypotheses for the control and function of male color. In the field, I found that Habronattus males indiscriminately court any female they encounter (including other species), so I first examined the role that colors play in species recognition. I manipulated male colors in H. pyrrithrix and found that while they are not required for species recognition, the presence of red facial coloration improves courtship success, but only if males are courting in the sun. Because light environment affects transmission of color signals, the multi- colored displays of males may facilitate communication in variable and unpredictable environments. Because these colors can be costly to produce and maintain, they also have the potential to signal reliable information about male quality to potential female mates. -
Biomechanics and Functional Morphology of Amblypygid Predation C J MCLEAN
Biomechanics and Functional Morphology of Amblypygid Predation C J MCLEAN PhD 2020 1 Biomechanics and Functional Morphology of Amblypygid Predation Callum McLean A thesis submitted in partial fulfilment of the requirements of the Manchester Metropolitan University for the degree of Doctor of Philosophy School of Science and the Environment Faculty of Science and Engineering The Manchester Metropolitan University 2020 2 Contents General Abstract - Acknowledgments - Chapter 1: Introduction - Introduction to Amblypygids - Arachnid Pedipalps - Amblypygid Pedipalps - Development of Sexual Dimorphism in Arachnids - Prey Capture in Arachnids - Prey Capture in Amblypygids - Summary and Thesis Aims - References - Chapter 2: Sexual Dimorphism in the Arachnid Orders - Abstract - Introduction - Aim/Survey Methodology - Standard figure abbreviations - Acari - 3 Amblypygi - Araneae - Palpigradi - Pseudoscorpiones - Opiliones - Ricinulei - Schizomida - Scorpiones - Solifugae - Uropygi - Discussion - Trends in SD across Arachnida - Selective pressures for SD in Arachnida - Conclusion - References - Appendix i - Supplementary material 1 - Supplementary material 2 - 4 Chapter 3: Sexual dimorphism in the size and shape of the raptorial pedipalps of Giant Whip Spiders (Arachnida: Amblypygi) - Abstract - Introduction - Materials and Methods - Results - Discussion - References - Appendix i - Supplementary material - Chapter 4: The Application of Elliptical Fourier Analysis to Quantify Patterns of Pedipalp Shape Complexity in a Diverse Sample of Amblypygid