The Sense of Sight in Spiders with Some Observations on the Color Sense
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Checklist of Spiders (Arachnida: Araneae) from India-2012
© Indian Society of Arachnology ISSN 2278 - 1587(Online) CHECKLIST OF SPIDERS (ARACHNIDA: ARANEAE) FROM INDIA-2012 Keswani, S.; P. Hadole and A. Rajoria* SGB Amravati University, Amravati-444602 [email protected]; [email protected] *Indraprastha University, Delhi; [email protected] ABSTRACT Spiders comprise one of the largest (5-6th) orders of animals. The spider fauna of India has never been studied in its entirety despite of contributions by many arachnologists since Stoliczka (1869). In the present paper, we provide an updated checklist of spiders from India based on published records and on the collections of the Arachnology Museum, SGB Amravati University. A total of 1686 species of spiders are now recorded from India. They belong to two infraorders, Mygalomorphae and Araneomorphae, 60 families and 438 genera. The list also includes 70 species from Karakorum. The spider diversity in India is dominated by Saltisids followed by Thomisids and then Araneids, Gnaphosids and Lycosids. Key words: India, Araneae, spider fauna, checklist. INTRODUCTION The pioneering contribution on the taxonomy of Indian spiders is that of European arachnologist Stoliczka (1869). Review of available literature reveals that the earliest contribution by Blackwall (1867); Karsch (1873); Simon (1887); Thorell (1895) and Pocock (1900) were the pioneer workers of Indian spiders. They described many species from India. Tikader (1980, 1982), Tikader, and Malhotra (1980) described spiders from India. Tikader (1980) compiled a book on Thomisid spiders of India, comprising two subfamilies, 25 genera and 115 species. Of these, 23 species were new to science. Descriptions, illustrations and distributions of all species were given. Keys to the subfamilies, genera, and species were provided. -
Australasian Arachnology 72
AAuusstrtraallaassiianan AArrachnachnoolloogygy Price $3 Number 72 ISSN 0811-3696 August 2005 Newsletter of Newsletter of the AustralasianArachnologicalSociety Australasian Arachnology No. 72 Page 2 THE AUSTRALASIAN ARTICLES ARACHNOLOGICAL SOCIETY The newsletter depends on your contributions! We encourage articles on a (www.australasian-arachnology.org) range of topics including current research activities, student projects, upcoming We aim to promote interest in the events or behavioural observations. ecology, behaviour and taxonomy of arachnids of the Australasian region. Please send articles to the editor: MEMBERSHIP Volker Framenau Department of Terrestrial Invertebrates Membership is open to amateurs, Western Australian Museum students and professionals, and is Locked Bag 49 managed by our Administrator: Welshpool, W.A. 6986, Australia. Richard J. Faulder [email protected] Agricultural Institute Yanco, New South Wales 2703. Format: i) typed or legibly printed on A4 Australia paper or ii) as text or MS Word file on email: [email protected] CD, 3½ floppy disk, or via email. Membership fees in Australian LIBRARY dollars, per 4 issues: The AAS has a large number of reference books, scientific journals and *discount standard institution papers available for loan or as Australia $8 $10 $12 photocopies, for those members who do NZ/PNG $10 $12 $14 not have access to a scientific library. elsewhere $12 $14 $16 Professional members are encouraged to There is no agency discount. send in their arachnological reprints. All postage is by airmail. *Discount rates apply to unemployed, pensioners Contact our librarian: and students (please provide proof of status). Jean-Claude Herremans Cheques are payable in Australian PO Box 291 dollars to “Australasian Arachnological Manly, New South Wales 1655. -
Neon Simon, 1876
Neon Simon, 1876 Taxonomy Neon is a widespread genus found in Europe, Africa, Asia and North America, as well as Australia where there are two species, Neon australis and N. taylori, as well as other undescribed species (Richardson unpubl.) Molecular data seems to link Neon to a large Australasian clade including Myrmarachne, Mopsus and Astia (Maddison 2015, Maddison et al Examples of live Neon 2008). Further information on the genus and described species can be found in Richardson and Illustrator (and ©) I.R. Macaulay Żabka (2017) and Whyte and Anderson (2017). Description Neon spp. are very small spiders, body length 3 mm, with an ovate abdomen. The head, viewed from above, is short and wide, widest at or just behind the posterior lateral eyes. These eyes may or may not overlap the sides of cephalothorax. The carapace is high, with a curving surface rising to a peak at the posterior lateral eyes and then dropping sharply to the rear. Chelicerae have a single (unident) retromarginal tooth and either one or none on the promargin. The first legs are longest, the fourth legs next longest. In N. australis, unlike N. taylori, the first legs are very strongly fringed. Aspects of the general morphology of Neon The male’s palp has a short tegulum with a proximal lobe. In N. australis, the long, thin embolus Illustrator (and ©) B.J. Richardson (CSIRO, begins with an anticlockwise spiral on the prolateral side of the palp. It then passes across the MP) distal edge of the tegulum before moving further distally to finish in a partial anticlockwise spiral near the tip of the cymbium. -
Relationship of Epigamic Display to the Systematics of Jumping Spiders (Araneae: Salticidae)
THE RELATIONSHIP OF EPIGAMIC DISPLAY TO THE SYSTEMATICS OF JUMPING SPIDERS (ARANEAE: SALTICIDAE) By DAVID B. RICHMAN A DISSERTATION PRESENTED TO THE GRADUATE COUNCIL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 1977 Dedicated to Dr. Joseph C. Bequaert and Dr. H. K. V/allace. ACKNOWLEDGEMENTS I wish to thank my committee members, Dr. Jonathan Reiskind, cha i rman, Dr. John F. Anderson, Dr. CI ifford Johnson, Dr. Dale H. Habeck and Dr. James E. Lloyd for their encouragement and criticism. I would also like to thank Dr. James T. Giesel, Dr. James L. Nation, Dr. Howard K. Wallace, and Dr. Henry M. Wallbrunn for suggestions or materials used in this study. Other people contributing specimens, materials, time or information include Dr. Bruce Cutler, G. B. Edwards, David E. Hill, Dr. Robert R. Jackson, Will Kopachik, Wayne Maddison, Randy Nicholson and Richard Skinner. 1 am indebted to both the Departments of Zoology and of Entomology and Nematology, University of Florida, for the use of their facilities Special thanks are due Dr. W. B. Miller, Dr. W. J. Gertsch and Mr. Vincent D. Roth for their advice while 1 was a graduate student at the University of Arizona. Part of the field work, especially that in south Florida, was supported by a Grant-in-Aid of Research from Sigma Xi . Finally, I wish to thank Ms. Lynda Coin for her advice and encouragement, without which much of the writing of this dissertation would have been more difficult V TABLE OF CONTENTS Page ACKNOWLEDEMENTS. -
Astia L. Koch, 1879
Astia L. Koch, 1879 Taxonomy Astia has one described Australian species: Astia hariola. Species previously listed in Astia have been transferred to other genera including Adoxotoma, Arasia, Cyrba, Helpis, Maevia and Sondra. A description of Heliophanus maculatus by Karsch in 1878 and figured in Wesolowska (1986) appears to be Astia hariola, removing Heliophanus from the Australian fauna. The genus Examples of live Astia is part of an Australasian clade (Maddison et al 2008, Gardzińska and Żabka 2010, Maddison Illustrators (and ©) G.J. Anderson (BR), R. 2015 including Adoxotoma, Arasia, Astilodes, Helpis, Jacksonoides, Megaloastia, Parahelpis, Whyte Sondra and Tauala. Genera from Indonesia (Katya) and the Philippines (Orthrus) may also be part of this group (Maddison 2015). Further information on the genus and described species can be found in Richardson and Żabka (2017) and Whyte and Anderson (2017). Description Astia hariola is a medium-sized spider, ranging in body length from 8 to 9 mm, with a moderately high cephalothorax. The head viewed from above is rectangular to pear-shaped, widest behind the posterior lateral eyes. From the side the carapace is horizontal until the posterior lateral eyes. The slender adult male has a cephalothorax wider than its abdomen Aspects of the general morphology of Astia while the female’s abdomen is wider than its cephalothorax. The chelicerae have several hariola retromarginal teeth (plurident) and three or more teeth on the promargin. Distinctive yellow- Illustrators (and ©) B.J. Richardson (CSIRO), orange markings at the rear of the abdomen in live animals fade to pale yellow or white when M. Żabka (diag,) preserved. -
Araneae: Salticidae
Zootaxa 2526: 37–53 (2010) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2010 · Magnolia Press ISSN 1175-5334 (online edition) A new genus and five new species of Astieae (Araneae: Salticidae) from Australia, with remarks on distribution JOANNA GARDZIŃSKA1 & MAREK ŻABKA Katedra Zoologii, Akademia Podlaska, 08–110 Siedlce, Poland 1Corresponding author. E-mail: [email protected] Abstract Parahelpis, a new genus of Astieae, is described for Helpis abnormis (Żabka, 2002) and Parahelpis smithae spec. nov., the former being designated the type species. Adoxotoma embolica spec. nov., A. nitida spec. nov., A. sexmaculata spec. nov., and Helpis longipalpis spec. nov. are described. Astia nodosa L. Koch, 1879 is transferred to Adoxotoma. Diagnoses and lists of species for Adoxotoma and Helpis are provided and remarks on their distribution are given. Key words: Australia, New Guinea, New Zealand, phylogeny, biogeography Introduction Over the last decade morphology-based salticid taxonomy has been refined with molecular data (Hedin & Maddison 2001; Maddison & Hedin 2003; Maddison et al. 2007, 2008). This has put a new light, not only on taxonomy, but also on the biogeographical history of taxa and faunas. The new approach has included information on a number of Australian/Australasian clades, the Astioida being one of them. Unexpectedly, it comprises genera such as Sandalodes Keyserling, Opisthoncus L. Koch, Simaetha Thorell, Neon Simon, Myrmarachne MacLeay and many others, previously classified in other subfamilies (Maddison et al. 2008). The Astieae clade itself is less controversial and its generic composition proposed by Wanless (1988) has largely been confirmed by the molecular results. -
The Life Cycle of Three Species of Portia (Salticidae, Spartaeinae)
THE CYCLE OF THREE SPECIES PORTIA. SALTIer ,SPARTAEINAE) SUSAN E A. HALLAS A thesis submitted in fulfillment of the for the Doctor of Phil in the University of Unive ty of 7 Ii , II i CONTENTS i/I I (I ~~' l page List of Tables iv List of Figures v Abstract 1 CHAPTER 1: INTRODUCTION 3 THE SALTICIDAE 3 PORTIA, AN ABERRANT SALTICID 3 CENTRAL QUESTIONS 5 PHYLOGENETIC STATUS OF PORTIA'S PECULIARITIES 5 PLAN OF THE THESIS 10 CHAPTER 2: HATCHING AND EARLY POST-EMBRYONIC DEVELOPMENT IN THE SALTICIDAE 12 INTRODUCTION 12 METHODS 13 TERMINOLOGY 14 RESULTS 15 ECLOSION 15 POST-HATCHING DEVELOPMENT 19 DEVELOPMENTAL TIMING 21 DISCUSSION 21 CHAPTER 3: LIFE HISTORY IN THE LABORATORY OF THREE SPECIES OF PORTIA, WEB-BUILDING ~UMPING SPIDERS (SALTICIDAE, ARANEAE) 25 INTRODUCTION 25 METHODS 26 RESULTS 27 APPEARANCE 27 MOULTING 28 AGE-SPECIFIC MORTALITY 31 SURVIVAL TO MATURITY 34 NUMBER OF INSTARS 34 INSTAR DURATION 34 MATURATION TIME 36 ADULT LONGEVITY 36 INTItASPECIFIC VARIATION IN GROWTH INCREMENT 36 ii INTERSPECIFIC VARIATION IN GROWTH INCREMENT 41 MORPHOLOGICAL INDICES OF SPECIES' GROWTH PATTERNS 43 DISCUSSION 43 MOULTING SURVIVAL AND MORTALITY 44 NUMBER OF INS TARS AND MATURATION TIME 46 INSTAR DURATION 48 ADULT LONGEVITY 48 GROWTH 50 CONCLUDING REMARKS 55 CHAPTER 4: OVIPOSITION BIOLOGY OF PORTIA, WEB-BUILDING JUMPING SPIDERS (ARANEAE, SALTICIDAE) 56 INTRODUCTION 56 METHODS 57 RESULTS 59 INTERSPECIFIC DIFFERENCES IN BATCH SIZE 59 ABDOMEN SIZE AND DISTENSION 61 VARIATION IN EGG SIZE 61 DIFFERENCES IN BATCH SIZE BETWEEN SEQUENTIAL BATCHES 65 TIMING OF OVIPOSITION 66 FERTILITY OF BATCHES 66 DISCUSSION 67 THE AFFECT OF LATITUDE 67 THE AFFECT OF FEMALE SIZE 69 THE AFFECT OF FORAGING STRATEGY 71 CONCLUSION 72 CHAPTER 5: THE ONTOGENY OF BEHAVIOUR IN PORTIA FIMBRIATA, P. -
Protective Resemblances in Spiders
Peckham, E. G. 1889. Protective resemblances in spiders. Occasional Papers of the Natural History Society of Wisconsin 1 (2): 61―113, Plates III―IV. Any notes added to the original text are indicated in red. Errors in the original text are indicated in blue. Pagination of the original document has been retained. Scientific names that were not italicized in the original have been italicized in this version. All illustrations are presented in their original size. No. 2.] PROTECTIVE RESEMBLANCES IN SPIDERS 61 PROTECTIVE RESEMBLANCES IN SPIDERS. ELIZABETH G. PECKHAM. Introduction. There are, among spiders, two forms of protective modification: the first, including all cases of protective resemblance to vegetable and inorganic things—that is, all modifications of color or of color and form that tend to make them inconspicuous in their natural relations —I shall call direct protection. The second form, which I shall call indirect protection, includes two classes, the spiders which are specially protected themselves and those which mimic other creatures which are specially protected.* Spiders are specially protected when they become inedible through the acquisition of hard plates and sharp spines. The modification of form is frequently accompanied by conspicuous colors, which warn their enemies that they belong to an unpalatable class.† The second class of indirectly protected spiders—those that mimic specially protected creatures—presents some difficulties, since it is not always easy to determine whether the purpose of mimicry is protection or the capture of prey. The resemblance may, as is frequently the case in direct protection, serve both purposes. In looking for instances of protective form and color among spiders we encounter one difficulty at the outset. -
Salticidae (Araneae) Genera of the World - an Atlas* (Unfinished Manuscript) Version September 7Th, 2020
0 Introduction 1 z 10 Main links: Title page Introduction & guides INDEXES_chapters_&_genera Open PDF printout of this file Salticidae (Araneae) genera of the world - an atlas* (unfinished manuscript) Version September 7th, 2020 by Jerzy Prószy ński Professor Emeritus, Museum and Institute of Zoology, Polish Academy of Sciences, ul. Wilcza 63, 00-679 Warsaw, POLAND e-mail: [email protected] After first thirty years of work, first visit in the MCZ-Harvard-1987 ABSTRACT. The aim of this paper is to display, within seconds, the most useful diagnostic characters of 641 recognizable genera of Salticidae, on the background of the whole diversity of the family. There is a possibility to compare them, also within seconds, with diversity of ca. 4800 recognizable species of these genera (which can be further followed by network of links to rich data of relational database including: geographical distribution, contents of collections, contents of publications, etc). The aim of grouping these genera is not to demonstrate phylogeny, or other fancy schemes, but they are assembled by similarities in palps, spermathecae and ducts for testing practical identification. Since my research are ".. nothing but scientific malpractice" (see motto below), this paper will be read only by the most intelligent and independent thinking arachnologists, who will understand perfectly the second bottom of this text. The unusual names of groups and genera used in this paper are intended to facilitate temporarily experimental shifting of genera in search for the most clear expression of similarities, they can be distinguished from those commonly used by being written in CAPITAL LETTERS and with different endings indicating their ranks. -
Family-Group Names in Diptera
Family-Group Names in Diptera Bibliography and Nota Bene: This is an exact copy of the material sent to the printers. Slight differences may be found in the pre- liminaries, such as this page which represents the copy for the spine. BUT the body of the work is an exact copy of the printed book. MYIA 10 1999 Family-Group Names in Diptera and Bibliography Backhuys Publishers Family-Group Names in Diptera and Bibliography MYIA The International Journal of the North American Dipterists’ Society Volume 10 Editor: F. Christian Thompson Review Committee Roger W. Crosskey Allen L. Norrbom Thomas Pape Published for North American Dipterists’ Society by Backhuys Publishers Family-Group Names in Diptera An annotated catalog. By Curtis W. Sabrosky Bibliography By F. Christian Thompson Neal L. Evenhuis Curtis W. Sabrosky North American Dipterists’ Society Backhuys Publishers Leiden 1999 Authors’ Addresses Neal L. Evenhuis Department of Natural Sciences B. Bishop Museum P. O. Box 19000 Honolulu, Hawaii 96817 USA Curtis W. Sabrosky Deceased Systematic Entomology Laboratory, USDA NHB-168 Smithsonian Institution Washington, D. C. 20560 USA F. Christian Thompson Sytematic Entomology Laboratory, USDA NHB-168 Smithsonian Institution Washington, D. C. 20560 USA ISBN 90-5782-???-? MYIA is devoted to dissemination of research and other information on flies (Diptera). The series was established by Paul H. Arnaud, Jr., and supported in part by the California Academy of Sciences. Five volumes have been published. The series is now jointly sponsored by the North American Dipterists’ Society, with individual volumes edited and produced either by Paul Arnaud at San Francisco or by Chris Thompson at Washington. -
Salticidae of the Antarctic Land Bridge 1
Peckhamia 76.1 Salticidae of the Antarctic land bridge 1 PECKHAMIA 76.1, 7 October 2009, 1―14 ISSN 1944―8120 Salticidae of the Antarctic land bridge David Edwin Hill 1 1 213 Wild Horse Creek Drive, Simpsonville, South Carolina 29680 Introduction At the breakup of Gondwanaland (~130―110 Ma), Africa, India, and Madagascar moved away from South America and Antarctica, with Australia still firmly conjoined to the latter (Figure 1). This movement left South America connected to Antarctica―Australia by a long isthmus (Ithmus of Scotia) of the southern Andes, at least from the Late Cretaceous (Campanian) through the Eocene (Yanbin 1998, Lawver et al. 1999, Sanmartín 2002). This Antarctic land bridge remained in place from the late Cretaceous through the Paleocene (65.5 ± 0.3 Ma to 55.8 ± 0.2 Ma) and Eocene (55.8 ± 0.2 to 33.9 ± 0.1 Ma) epochs. At times it may have included short island arcs at either the Australian (Tasmanian) or South American ends. This land bridge, associated with a tropical to temperate Antarctic climate (Francis et al. 2008), was thus available to support the dispersal of plant and animal species for about 75 to 95 million years after the separation of Africa, a very long time. One very interesting aspect about this interval is that it also brackets the mass extinction event at the end of the Cretaceous. According to Penney et al. (2003), however, that event did nothing to reduce the diversity of spiders as a group. Figure 1. Cretaceous (top) and Eocene (bottom) reconstructions of Earth topography and bathymetry. -
Sunda to Sahul: Trans-Wallacean Distribution of Recent Salticid Genera (Araneae: Salticidae)1
Peckhamia 80.1 Trans-Wallacean distribution of salticid genera 1 PECKHAMIA 80.1, 19 May 2010, 1―60 ISSN 1944―8120 Sunda to Sahul: Trans-Wallacean distribution of recent salticid genera (Araneae: Salticidae)1 David Edwin Hill 2 1 Figures in this collection appear by permission of copyright owners. See the Figure Attribution section for more details. 2 213 Wild Horse Creek Drive, Simpsonville, South Carolina 29680-6513, USA, email [email protected] Summary From Southeast Asia to Australia, the published distribution of recent salticid genera reflects a major division between a large and diverse Australian (Sahulian) fauna including many astioids, cocalodines and euophryines, and a large and diverse tropical Asian (Sundan) fauna including many heliophanines, plexippoids and spartaeines. The tropical Asian fauna shares many genera with tropical Africa. As with many other plant and animal groups, this pattern appears to reflect the long-term isolation of these two faunas. A limited number of recent genera and species have been successful in traversing the island archipelago (Wallacea) connecting these two biogeographic provinces. As part of Sahul, the island of New Guinea is the center of diversity for a number of unusual salticids. This may be the result of a diverse and persistent tropical environment that has served as a refugium for 'relict' or otherwise unusual species. It may also point to the accretion of isolated island arcs and associated faunas, a result of the post-Eocene movement of the Australian plate. In contrast, the known salticid fauna of temperate New Zealand exhibits little diversity, and appears to be comprised largely of astioid species placed within several widely-distributed, trans-oceanic Australian genera.