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Molecular Phylogeny, Divergence Times and Biogeography of Spiders of the Subfamily Euophryinae (Araneae: Salticidae) ⇑ Jun-Xia Zhang A, , Wayne P
Molecular Phylogenetics and Evolution 68 (2013) 81–92 Contents lists available at SciVerse ScienceDirect Molec ular Phylo genetics and Evolution journal homepage: www.elsevier.com/locate/ympev Molecular phylogeny, divergence times and biogeography of spiders of the subfamily Euophryinae (Araneae: Salticidae) ⇑ Jun-Xia Zhang a, , Wayne P. Maddison a,b a Department of Zoology, University of British Columbia, Vancouver, BC, Canada V6T 1Z4 b Department of Botany and Beaty Biodiversity Museum, University of British Columbia, Vancouver, BC, Canada V6T 1Z4 article info abstract Article history: We investigate phylogenetic relationships of the jumping spider subfamily Euophryinae, diverse in spe- Received 10 August 2012 cies and genera in both the Old World and New World. DNA sequence data of four gene regions (nuclear: Revised 17 February 2013 28S, Actin 5C; mitochondrial: 16S-ND1, COI) were collected from 263 jumping spider species. The molec- Accepted 13 March 2013 ular phylogeny obtained by Bayesian, likelihood and parsimony methods strongly supports the mono- Available online 28 March 2013 phyly of a Euophryinae re-delimited to include 85 genera. Diolenius and its relatives are shown to be euophryines. Euophryines from different continental regions generally form separate clades on the phy- Keywords: logeny, with few cases of mixture. Known fossils of jumping spiders were used to calibrate a divergence Phylogeny time analysis, which suggests most divergences of euophryines were after the Eocene. Given the diver- Temporal divergence Biogeography gence times, several intercontinental dispersal event sare required to explain the distribution of euophry- Intercontinental dispersal ines. Early transitions of continental distribution between the Old and New World may have been Euophryinae facilitated by the Antarctic land bridge, which euophryines may have been uniquely able to exploit Diolenius because of their apparent cold tolerance. -
FNN 314 Final Version.Pub
Field Nats News No.314 Newsletter of the Field Naturalists Club of Victoria Inc. Editor: Joan Broadberry 03 9846 1218 1 Gardenia Street, Blackburn Vic 3130 Founding editor: Dr Noel Schleiger Telephone 03 9877 9860 Reg. No. A0033611X P.O. Box 13, Blackburn 3130 www.fncv.org.au Understanding Patron: The Honourable Linda Dessau, AC Our Natural World Newsletter email: [email protected] Est. 1880 (Office email: [email protected]) Governor of Victoria Office Hours: Monday and Tuesday 10.00 am - 4 pm. December 2020/January 2021 This is the last FNN for 2020 and I would From the President like to thank and congratulate the editorial As this issue covers two months, team for a sterling effort under very trying December 2020 and January circumstances. I encourage everyone to continue sending photos and observations 2021, the due date for FNN 315 to Joan for inclusion in forthcoming editions. I wish you all a safe and productive (the February edition) will be holiday season and hope to see you in person in 2021 when possible. 10 am Tuesday 5th January 2021. We will be upgrading the washrooms/toilets at the hall over the break to provide safe hand washing facilities as part of a covid-19 safety management strategy. A hot water system will be installed along with hands-free taps, hands-free soap dispensers and hands-free air dryers. Where possible, hands-free door opening will be adopted. The final procedures and overall strategy will depend upon the current regulatory requirements. We have been running a number of successful Zoom meetings and presentations and expect to continue them as needed in 2021 and beyond. -
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. -
A Taxonomical Study of the Japanese Spider Hitherto Misidentified with Argiope Keyserlingi (KARSCH, 1878) Or A, Aetherea (WALCKE
Acta arachnol., 43 (1): 33-36, June 30, 1994 A Taxonomical Study of the Japanese Spider Hitherto Misidentified with Argiope keyserlingi (KARSCH,1878) or A, aetherea (WALCKENAER,1841) Akio TANIKAWAI~ 谷 川 明 男1):ム シバ ミ コガ ネ グ モ の 分 類 学 的 検 討 Abstract The orb-web spider, Argiope aetheroides YIN et al., 1989, is recorded from Japan. The spiders of the species have been wrongly identified with Argiope keyserlingi (KARSCH, 1878) or Argiope aetherea (WALCKENAER,1841) by the previous Japanese authors. When LEvI (1983) revised the spiders of the genera Argiope, Gea and Neogea from the Western Pacific region including Japan, he examined 6 Japanese species : Argiope aemula (WALCKENAER,1841), A. boesenbergi LEVI,1983, A. amoena L. KOCH, 1878, A. bruennichii (SCOPOLI,1772), A. minuta KARSCH,1879, and A. ocula Fox, 1938. Moreover, a doubtful species of the genus is occurring in Japan, which has been identified either with A. keyserlingi (KARSCH,1878) (KISHIDA,1936;YAGINUMA, 1968, 1970, 1977; YAGINUMA& SHINKAI,1971) or with A. aetherea (WALCKENAER, 1841) (SHINKAI& TAKANO,1984, 1987; YAGINUMA,1986; YAGINUMAet al., 1990). In 1990, I collected female and male specimens of the species from Yakushima Island, Kagoshima Pref., Japan, and could confirm the fact that the features of these specimens did not agree with LEVI's (1983) redescriptions and figures of A. keyserlingi and A. aetherea. Then, many specimens of the species were offered by colleagues and collected by myself. After a careful examination of these materials, I came to the conclusion that the species was neither A. keyserlingi nor A. -
Visual Perception in Jumping Spiders (Araneae,Salticidae)
Visual Perception in Jumping Spiders (Araneae,Salticidae) A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of Philosophy in Biology at the University of Canterbury by Yinnon Dolev University of Canterbury 2016 Table of Contents Abstract.............................................................................................................................................................................. i Acknowledgments .......................................................................................................................................................... iii Preface ............................................................................................................................................................................. vi Chapter 1: Introduction ................................................................................................................................................... 1 Chapter 2: Innate pattern recognition and categorisation in a jumping Spider ........................................................... 9 Abstract ....................................................................................................................................................................... 10 Introduction ................................................................................................................................................................ 11 Methods ..................................................................................................................................................................... -
An International Peer Reviewed Open Access Journal for Rapid Publication
VOLUME-12 NUMBER-4 (October-December 2019) Print ISSN: 0974-6455 Online ISSN: 2321-4007 CODEN: BBRCBA www.bbrc.in University Grants Commission (UGC) New Delhi, India Approved Journal An International Peer Reviewed Open Access Journal For Rapid Publication Published By: Society for Science & Nature (SSN) Bhopal India Indexed by Thomson Reuters, Now Clarivate Analytics USA ISI ESCI SJIF=4.186 Online Content Available: Every 3 Months at www.bbrc.in Registered with the Registrar of Newspapers for India under Reg. No. 498/2007 Bioscience Biotechnology Research Communications VOLUME-12 NUMBER-4 (Oct-Dec 2019) Characteristics of Peptone from the Mackerel, Scomber japonicus Head by-Product as Bacterial Growth Media 829-836 Dwi Setijawati, Abdul A. Jaziri, Hefti S. Yufidasari, Dian W. Wardani, Mohammad D. Pratomo, Dinda Ersyah and Nurul Huda Endomycorrhizae Enhances Reciprocal Resource Exchange Via Membrane Protein Induction 837-843 Faten Dhawi Does Prediabetic State Affects Dental Implant Health? A Systematic Review And Meta-Analysis 844-854 Khulud Abdulrahman Al-Aali An Updated Review on the Spiders of Order Araneae from the Districts of Western Ghats of India 855-864 Misal P. K, Bendre N. N, Pawar P. A, Bhoite S. H and Deshpande V. Y Synergetic Role of Endophytic Bacteria in Promoting Plant Growth and Exhibiting Antimicrobial 865-875 Mbarek Rahmoun and Bouri Amira Synergetic Role of Endophytic Bacteria in Promoting Plant Growth and Exhibiting 876-882 Antimicrobial Activities Bassam Oudh Al Johny Influence on Diabetic Pregnant Women with a Family History of Type 2 Diabetes 883-888 Sameera A. Al-Ghamdi Remediation of Cadmium Through Hyperaccumulator Plant, Solanum nigrum 889-893 Ihsan Ullah Biorefinery Sequential Extraction of Alginate by Conventional and Hydrothermal Fucoidan from the 894-903 Brown Alga, Sargassum cristaefolium Sugiono Sugiono and Doni Ferdiansyah Occupational Stress and Job Satisfaction in Prosthodontists working in Kingdom of Saudi Arabia 904-911 Nawaf Labban, Sulieman S. -
Molecular Insights Into the Phylogenetic Structure of the Spider
MolecularBlackwell Publishing Ltd insights into the phylogenetic structure of the spider genus Theridion (Araneae, Theridiidae) and the origin of the Hawaiian Theridion-like fauna MIQUEL A. ARNEDO, INGI AGNARSSON & ROSEMARY G. GILLESPIE Accepted: 9 March 2007 Arnedo, M. A., Agnarsson, I. & Gillespie, R. G. (2007). Molecular insights into the phylo- doi:10.1111/j.1463-6409.2007.00280.x genetic structure of the spider genus Theridion (Araneae, Theridiidae) and the origin of the Hawaiian Theridion-like fauna. — Zoologica Scripta, 36, 337–352. The Hawaiian happy face spider (Theridion grallator Simon, 1900), named for a remarkable abdominal colour pattern resembling a smiling face, has served as a model organism for under- standing the generation of genetic diversity. Theridion grallator is one of 11 endemic Hawaiian species of the genus reported to date. Asserting the origin of island endemics informs on the evolutionary context of diversification, and how diversity has arisen on the islands. Studies on the genus Theridion in Hawaii, as elsewhere, have long been hampered by its large size (> 600 species) and poor definition. Here we report results of phylogenetic analyses based on DNA sequences of five genes conducted on five diverse species of Hawaiian Theridion, along with the most intensive sampling of Theridiinae analysed to date. Results indicate that the Hawai- ian Islands were colonised by two independent Theridiinae lineages, one of which originated in the Americas. Both lineages have undergone local diversification in the archipelago and have convergently evolved similar bizarre morphs. Our findings confirm para- or polyphyletic status of the largest Theridiinae genera: Theridion, Achaearanea and Chrysso. -
Araneae, Theridiidae)
Phelsuma 14; 49-89 Theridiid or cobweb spiders of the granitic Seychelles islands (Araneae, Theridiidae) MICHAEL I. SAARISTO Zoological Museum, Centre for Biodiversity University of Turku,FIN-20014 Turku FINLAND [micsaa@utu.fi ] Abstract. - This paper describes 8 new genera, namely Argyrodella (type species Argyrodes pusillus Saaristo, 1978), Bardala (type species Achearanea labarda Roberts, 1982), Nanume (type species Theridion naneum Roberts, 1983), Robertia (type species Theridion braueri (Simon, 1898), Selimus (type species Theridion placens Blackwall, 1877), Sesato (type species Sesato setosa n. sp.), Spinembolia (type species Theridion clabnum Roberts, 1978), and Stoda (type species Theridion libudum Roberts, 1978) and one new species (Sesato setosa n. sp.). The following new combinations are also presented: Phycosoma spundana (Roberts, 1978) n. comb., Argyrodella pusillus (Saaristo, 1978) n. comb., Rhomphaea recurvatus (Saaristo, 1978) n. comb., Rhomphaea barycephalus (Roberts, 1983) n. comb., Bardala labarda (Roberts, 1982) n. comb., Moneta coercervus (Roberts, 1978) n. comb., Nanume naneum (Roberts, 1983) n. comb., Parasteatoda mundula (L. Koch, 1872) n. comb., Robertia braueri (Simon, 1898). n. comb., Selimus placens (Blackwall, 1877) n. comb., Sesato setosa n. gen, n. sp., Spinembolia clabnum (Roberts, 1978) n. comb., and Stoda libudum (Roberts, 1978) n. comb.. Also the opposite sex of four species are described for the fi rst time, namely females of Phycosoma spundana (Roberts, 1978) and P. menustya (Roberts, 1983) and males of Spinembolia clabnum (Roberts, 1978) and Stoda libudum (Roberts, 1978). Finally the morphology and terminology of the male and female secondary genital organs are discussed. Key words. - copulatory organs, morphology, Seychelles, spiders, Theridiidae. INTRODUCTION Theridiids or comb-footed spiders are very variable in general apperance often with considerable sexual dimorphism. -
Tarantulas and Social Spiders
Tarantulas and Social Spiders: A Tale of Sex and Silk by Jonathan Bull BSc (Hons) MSc ICL Thesis Presented to the Institute of Biology of The University of Nottingham in Partial Fulfilment of the Requirements for the Degree of Doctor of Philosophy The University of Nottingham May 2012 DEDICATION To my parents… …because they both said to dedicate it to the other… I dedicate it to both ii ACKNOWLEDGEMENTS First and foremost I would like to thank my supervisor Dr Sara Goodacre for her guidance and support. I am also hugely endebted to Dr Keith Spriggs who became my mentor in the field of RNA and without whom my understanding of the field would have been but a fraction of what it is now. Particular thanks go to Professor John Brookfield, an expert in the field of biological statistics and data retrieval. Likewise with Dr Susan Liddell for her proteomics assistance, a truly remarkable individual on par with Professor Brookfield in being able to simplify even the most complex techniques and analyses. Finally, I would really like to thank Janet Beccaloni for her time and resources at the Natural History Museum, London, permitting me access to the collections therein; ten years on and still a delight. Finally, amongst the greats, Alexander ‘Sasha’ Kondrashov… a true inspiration. I would also like to express my gratitude to those who, although may not have directly contributed, should not be forgotten due to their continued assistance and considerate nature: Dr Chris Wade (five straight hours of help was not uncommon!), Sue Buxton (direct to my bench creepy crawlies), Sheila Keeble (ventures and cleans where others dare not), Alice Young (read/checked my thesis and overcame her arachnophobia!) and all those in the Centre for Biomolecular Sciences. -
ASH Newsletter 45.Pub
THE AUSTRALIAN SOCIETY OF HERPETOLOGISTS INCORPORATED NEWSLETTER 45 2 3 History of Office Bearers Formation Committee (April 1964):- MJ Littlejohn (Convenor); State Reps IR Straughan (Qld), FJ Mitchell (SA), HG Cogger (NSW), G Storr (WA), RE Barwick (ACT), JW Warren (Vic), AK Lee (Editor). First AGM (23 August 1965):- President MJ Littlejohn, Vice-President NG Stephenson, Secretary-Treasurer AA Martin, Asst Secretary-Treasurer KJ Wilson, Ordinary Members FJ Mitchell and IR Straughan, Editor AK Lee. PRESIDENT:- MJ Littlejohn (1965-69); AK Lee (1969-70); HG Cogger (1971-73); J de Bavay (1974); H Heat- wole (1975-76); GC Grigg (1976-77); MJ Tyler (1978-79); GF Watson (1979-81); AA Martin (1981-82); RS Seymour (1982-83); R Shine (1983-84); GC Grigg (1984-86); J Coventry (1986-87); RE Barwick (1987-88); J Covacevich (1988-91); M Davies (1991-92); R Shine (1992-94); A Georges (1994-6); D Roberts (1996-98); M Bull (1998-9); R Swain (1999-2001); S Downes (2001-03); J Melville (2004-2005); J-M Hero (2005-2007); P Doherty (2007-2008); M Thompson (2008-2009); M Hutchinson (2009-) VICE-PRESIDENT:- NG Stephenson (1965-67); RE Barwick (1967-69); HG Cogger (1969-70); MJ Littlejohn (1971-72); MJ Tyler (1973); HG Cogger (1974); J de Bavay (1975-76); H Heatwole (1976-77); GC Grigg (1977 -79); MJ Tyler (1979-80); GF Watson (1981-82); AA Martin (1982-83); RS Seymour (1983-84); R Shine (1984- 86); GC Grigg (1986-87); J Coventry (1987-88); RE Barwick (1988-91); J Covacevich (1991-92); M Davies (1992-94); R Shine (1994-6); A Georges (1996-98); D Roberts (1998-99); M Bull(1999-2001); R Swain (2001- 2003); S Downes (2004-5); J Melville (2005-2007); J-M Hero (2007-2008); P Doherty (2008-2009); M Thomp- son (2009-) SECRETARY/TREASURER:- AA Martin (1965-67); GF Watson (1967-72); LA Moffatt (1973-75); J Caughley (1975-76); RWG Jenkins (1976-77); M Davies (1978-83); G Courtice (1983-87); J Wombey (1987-99); S Ke- ogh (1999-2003); N Mitchell (2004-5). -
Zabka and Pollard, 2002
~ ~". ..,M ~.J * Marek Zabka' and Simon D Pollard' kf ~flPls ~~ SaIticidae (Arachnida:Araneae) of New Zealand: genus Hypoblemum Peckham and Peckham, 1886 Abstract The genus Hypoblemum is redefined and H. Collections studied: a/boviuotum (Keyserling, 1882) is recorded from New AMNZ - Auckland Museum Entomology Collection (John Zealand. Remarks on relationships, biology and distribution Early), ofthe genus are provided and adistributional map is given. CMC - Canterbury Museum, Christchurch (Simon Pollard), Keywords Salticidae, Hypoblemllnl, taxonomy, biogeogra· cue - Canterbury University, Christchurch (Robert phy, New Zealand Jackson & Mathew Anstey), now dcposited in CMC, LUNZ· Entomology Research Museum, Lincoln Univer Introduction sity, Lincoln (Cor Vink), MNZ - Museum of New Zealand Te Papa, Wellington (Phil The taxonomic research ofNew Zealand jumping spiders Sirvid). (Salticidae) began well over acentury ago and until now, NZAC - New Zealand Arthropod Collection, Auckland some 50 species have been described or recorded. However, (Trevor Crosby), the lack oftype specimens, poor original diagnoses, great OMD - Otago Museum, Dunedin (Brian Patrick, Erena intraspecific variation in size and colour and interspecific Barker & Simon Wylie), uniformity in genitalic structure make proper verific3tion of 2MB - Museum fUr Naturkunde der Humboldt species a very difficuh task. Consequently, less than 10 Universitiit, Berlin (Jason Dunlop), New Zealand species are recognisable - usually under ZMH - Zoologisehes Institut und Zoologisehes Museum, wrong generic names (e. g., Marpissa, Altus or Euophrys). Universitiit Hamburg (Hieronymus Dastyeh). Recent field research and the study of major spider collections (see below) revealed that about 30 genera and Taxonomic review 200 species ofSaltieidae occur in New Zealand (Zabka unpub1.), most of them endemics. Despite expectations, Gen. Hypab/ellllllll Peckham et Peckham, 1886 only selected Australian genera reached New Zealand Hypab/emllm Peckham & Peckham, 1886: 271. -
Mai Po Nature Reserve Management Plan: 2019-2024
Mai Po Nature Reserve Management Plan: 2019-2024 ©Anthony Sun June 2021 (Mid-term version) Prepared by WWF-Hong Kong Mai Po Nature Reserve Management Plan: 2019-2024 Page | 1 Table of Contents EXECUTIVE SUMMARY ................................................................................................................................................... 2 1. INTRODUCTION ..................................................................................................................................................... 7 1.1 Regional and Global Context ........................................................................................................................ 8 1.2 Local Biodiversity and Wise Use ................................................................................................................... 9 1.3 Geology and Geological History ................................................................................................................. 10 1.4 Hydrology ................................................................................................................................................... 10 1.5 Climate ....................................................................................................................................................... 10 1.6 Climate Change Impacts ............................................................................................................................. 11 1.7 Biodiversity ................................................................................................................................................