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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. -
19 3 153 188 Proszynski for Inet.P65
Arthropoda Selecta 19(3): 153188 © ARTHROPODA SELECTA, 2010 Description of some Salticidae (Araneae) from the Malay Archipelago. I. Salticidae of the Lesser Sunda Islands, with comments on related species Îïèñàíèå íåêîòîðûõ Salticidae (Araneae) èç Ìàëàéñêîãî Àðõèïåëàãà. I. Salticidae Ìàëûõ Çîíäñêèõ îñòðîâîâ ñ êîììåíòàðèÿìè î áëèçêèõ âèäàõ Jerzy Prószyñski*, Christa L. Deeleman-Reinhold** É. Ïðóøèíüñêèé*, Ê. Äèëåìàí-Ðåéíîëüä** * Museum and Institute of Zoology, Polish Academy of Sciences, ul. Wilcza 64, 00-679 Warszawa, Poland. E-mail: jerzy.Prószyñ[email protected] ** 4619GA Ossendrecht, the Netherlands. E-mail: [email protected] KEY WORDS: Salticidae, new species, diagnostic characters, geographical distribution, Indonesia, Bali, Flores, Lombok, Sumba, Sumbawa. ÊËÞ×ÅÂÛÅ ÑËÎÂÀ: íîâûé âèä, äèàãíîñòè÷åñêèå ïðèçíàêè, ðàñïðîñòðàíåíèå, Èíäîíåçèÿ, î. Áàëè, î. Ôëîðåñ, î. Ëîìáîê, î. Ñóìáà, î. Ñóìáàâà. In memoriam Bohdan Pisarski, friend of J. Prószyñski and com- panion in the Java and Bali collecting trip in 1959, for many years the Director of the Institute of Zoology PAN. ABSTRACT. This paper provides preliminary ref- Myrmarachne MacLeay, 1839 is discussed. Comple- erence diagnostic drawings for selected Oriental gen- mentary diagnostic drawings are added for the fol- era and species, to complement the existing scanty lowing species: Artabrus erythrocephalus (C.L. Koch, literature. The following new taxa are described: new 1846), Harmochirus brachiatus (Thorell, 1877), genus Katya gen.n., new species: Burmattus Hasarius adansoni (Audouin, 1826), Myrmarachne pachytibialis sp.n., Carrhotus sundaicus sp.n., Chrysilla hirsutipalpi [?] Edmunds & Prószyñski, 2003, Spar- deelemani sp.n., Cosmophasis valerieae sp.n., Cytaea taeus spinimanus (Thorell, 1878), Thiania bhamoen- whytei sp.n., Euryattus [?] junxiae sp.n., Katya flore- sis Thorell, 1887. -
Araneae: Salticidae)
Doctoral Thesis Taxonomic revision of Vietnamese species of the genus Phintella Strand (Araneae: Salticidae) Phung Thi Hong Luong Department of Biological Sciences, Graduate School of Science and Engineering, Tokyo Metropolitan University, Minami–Osawa 1–1, Hachioji, Tokyo 192–0397, Japan September in 2017 1 首都大学東京 博士(理学)学位論文(課程博士) 論 文 名 ベトナム産ヤマトハエトリグモ属(クモ目:ハエトリグモ科) の分類学的再検討 (英文) 著 者 フオン テイ ホン ロン 審査担当者 主 査 委 員 委 員 委 員 上記の論文を合格と判定する 平成 年 月 日 首都大学東京大学院理工学研究科教授会 研究科長 DISSERTATION FOR A DEGREE OF DOCTOR OF PHILOSOPHY IN SCIENCE TOKYO METROPOLITAN UNIVERSITY TITLE:Taxonomic revision of Vietnamese species of the genus Phintella Strand (Araneae: Salticidae) AUTHOR:Phung Thi Hong Luong EXAMINED BY Examiner in chief Examiner Examiner Examiner QUALIFIED BY THE GRADUATE SCHOOL OF SCIENCE AND ENGINEERING TOKYO METROPOLITAN UNIVERSITY Dean Date 0 Summary Spiders (the order Araneae) are dominant predatory arthropods in terrestrial ecosystems. The family Salticidae (jumping spiders) is the largest family of spiders; it is known throughout the world, and consists of nearly 6,000 described species belonging to 625 genera, holding 13% of all species of spiders (Foelix, 1996; Jackson et al., 2001). Salticids usually show distinct sexual dimorphism in morphology of the adults. As a result, the male-female complementarity remains unclear for many nominal species in this family. This means that more than a few synonymies are likely hidden in the current classification of the family. Furthermore, due to insufficient sampling efforts in tropical and subtropical zones, it is likely that many species are yet to be discovered. The genus Phintella Strand in Bösenberg and Strand (1906) is one of the most speciose genera in the family Salticidae, and is thought to have diversified in the Oriental and Palearctic regions. -
Biodiversity : Exploration, Exploitation, Conservation and Management – Vision and Mission”
-2- “Biodiversity : Exploration, Exploitation, Conservation and Management – Vision and Mission” Proceedings of the UGC Sponsored National Seminar 19-20th November, 2016 Editor-in-Chief Dr. Sumana Saha Associate Editors Dr. Madhumita Manna, Dr. Jayati Ghosh, Dr. Sanjoy Podder, Dr. Enamul Haque Dr. Srikanta Guria, Sri Somaditya Dey Organised by Post Graduate Department of Zoology Barasat Government College Barasat, Kolkata – 700 124, India In Collaboration with The Zoological Society, Kolkata West Bengal Biodiversity Board -3- Citation S. Saha, M. Manna, J. Ghosh, S. Podder, E. Haque, S. Guria and S. Dey (Eds.). Biodiversity : Exploration, Exploitation, Conservation and Management - Vision and Mission. Proceedings of the UGC Sponsored National Seminar, Kolkata, India, 19-20th November, 2016. World Scientific News 71 (2017) 1-228 Reviewer Prof. Jerzy Borowski Department of Forest Protection and Ecology, SGGW, Warsaw, Poland Published On-line 03 May, 2017, WSN Volume 71 (2017), pp. 1-228 http://www.worldscientificnews.com/ Published By Dr. Tomasz Borowski Scientific Publishing House „DARWIN”, 22/12 Adama Mickiewicza Street, 78-520 Złocieniec, Poland ISBN 978-83-947896-2-6 ISSN 2392-2192 Technical Inputs Ruby Das All Rights Reserved No part/s of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the prior permission of the publisher. Cover Design Dr. Sumana Saha -4- Contents SECTION : I Page no. 1. Message ................................................................................................................... -
First Record of Thiania Cf. Subopressa Strand 1907 (Araneae: Salticidae: Euophryini) from India with Some Natural History Notes on the Species
Peckhamia 214.1 Thiania cf. subopressa from India 1 PECKHAMIA 214.1, 15 July 2020, 1―5 ISSN 2161―8526 (print) LSID urn:lsid:zoobank.org:pub:1600BFFE-D067-41D9-B4A2-452BA5092EA6 (registered 13 JUL 2020) ISSN 1944―8120 (online) First record of Thiania cf. subopressa Strand 1907 (Araneae: Salticidae: Euophryini) from India with some natural history notes on the species Javed Ahmed 1, Atanu Chakraborti 2 and David E. Hill 3 1 Jai Gopi Krishna CHSL, 'A' Wing, Flat No. 102. 1, Patil Wadi, Govandi East, Mumbai 400088, India, email [email protected] 2 Asst. Conservator of Forests, Tripura; The Divisional Manager, T. F. D. P. C. Bhavan, Room no. 304, Abhoynagar, Near to AG Office, Agartala, Tripura, Pin -799005, India, email [email protected] 3 213 Wild Horse Creek Drive, Simpsonville, South Carolina, 29680, USA, email [email protected] The genus Thiania C. L. Koch 1846 is a primarily oriental genus of relatively large salticids, possessing a broad, depressed prosoma and a slender opisthosoma, with an overall flattened body bearing lustrous markings made up of iridescent, scale-like hairs. These spiders are also sometimes referred to as fighting spiders because of the combative nature of the males, in which the first pair of legs is often greatly elongated (Zabka 1985; Murphy & Murphy, 2000; Li et. al. 2002; Suguro 2012). Although the genus Thiania now includes 23 species, only a single species has hitherto been recorded in India, T. bhamoensis Thorell 1887 (WSC 2020). Here we report the occurrence of Thiania cf. subopressa, only the second species in the genus to be photographed in this country (Figures 1-2). -
Euophryines [Pdf]
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) a, a,b Jun-Xia Zhang ⇑, Wayne P. Maddison 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 a b s t r a c t 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. -
Journal of Threatened Taxa ISSN 0974-7907 (Online) ISSN 0974-7893 (Print)
Journal of Threatened Taxa ISSN 0974-7907 (Online) ISSN 0974-7893 (Print) 26 July 2019 (Online & Print) PLATINUM Vol. 11 | No. 9 | 14087–14246 OPEN 10.11609/jott.2019.11.9.14087-14246 ACCESS www.threatenedtaxa.org J Building TTevidence for conservation globally ISSN 0974-7907 (Online); ISSN 0974-7893 (Print) Publisher Host Wildlife Information Liaison Development Society Zoo Outreach Organization www.wild.zooreach.org www.zooreach.org No. 12, Thiruvannamalai Nagar, Saravanampatti - Kalapatti Road, Saravanampatti, Coimbatore, Tamil Nadu 641035, India Ph: +91 9385339863 | www.threatenedtaxa.org Email: [email protected] EDITORS Typesetting Founder & Chief Editor Mr. Arul Jagadish, ZOO, Coimbatore, India Dr. Sanjay Molur Mrs. Radhika, ZOO, Coimbatore, India Wildlife Information Liaison Development (WILD) Society & Zoo Outreach Organization (ZOO), Mrs. Geetha, ZOO, Coimbatore India 12 Thiruvannamalai Nagar, Saravanampatti, Coimbatore, Tamil Nadu 641035, India Mr. Ravindran, ZOO, Coimbatore India Deputy Chief Editor Fundraising/Communications Dr. Neelesh Dahanukar Mrs. Payal B. Molur, Coimbatore, India Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, India Editors/Reviewers Managing Editor Subject Editors 2016-2018 Mr. B. Ravichandran, WILD, Coimbatore, India Fungi Associate Editors Dr. B.A. Daniel, ZOO, Coimbatore, Tamil Nadu 641035, India Dr. B. Shivaraju, Bengaluru, Karnataka, India Ms. Priyanka Iyer, ZOO, Coimbatore, Tamil Nadu 641035, India Prof. Richard Kiprono Mibey, Vice Chancellor, Moi University, Eldoret, Kenya Dr. Mandar Paingankar, Department of Zoology, Government Science College Gadchiroli, Dr. R.K. Verma, Tropical Forest Research Institute, Jabalpur, India Chamorshi Road, Gadchiroli, Maharashtra 442605, India Dr. V.B. Hosagoudar, Bilagi, Bagalkot, India Dr. Ulrike Streicher, Wildlife Veterinarian, Eugene, Oregon, USA Dr. Vatsavaya S. -
How Resources Control Aggression in Drosophila
How resources control aggression in Drosophila Thesis by Rod S. Lim In Partial Fulfillment of the Requirements for the degree of Doctor of Philosophy CALIFORNIA INSTITUTE OF TECHNOLOGY Pasadena, California ii 2015 (Defended [August 28, 2014]) © 2014 Rod S Lim All Rights Reserved iii ACKNOWLEDGEMENTS First of all, I would like to thank my advisor, Dr. David Anderson, for his continued encouragement and support. In the Fall of 2007, fresh out of my first neuroscience course, I snuck into a conference at the Salk Institute called “Genes, Circuits and Behavior” and heard my sponsor Dr. David Anderson’s talk. I still remember the first part of his presentation vividly, when he presented his work identifying neural circuits controlling fear-like behavior in Drosophila. During these special four days, I decided to become a neuroscientist and hoped to work for Dr. Anderson one day. A year later, after visiting eight different campuses for graduate school interviews, a visit to Dr. Anderson’s lab cemented my decision. There were many ups and downs throughout the last five years, most notably the unexpected family tragedies. Despite my struggles, David was patient and would not give up on me. His relentless passion and energy for science propelled me to get through the trying times; I am forever indebted to his persevering support. In addition to my advisor, I would like to thank the members of my thesis committee: Drs. Pietro Perona, Paul Sternberg, and Kai Zinn. They were always there for counsel whenever I needed them, and I am truly grateful for their scientific and personal support. -
Araneae: Salticidae
The Biogeography and Age of Salticid Spider Radiations with the Introduction of a New African Group (Araneae: Salticidae). by Melissa R. Bodner B.A. (Honours) Lewis and Clark College, 2004 A THESIS SUBMITTED IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in The Faculty of Graduate Studies (Zoology) THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) July 2009 © Melissa R. Bodner 2009 ABSTRACT Globally dispersed, jumping spiders (Salticidae) are species-rich and morphologically diverse. I use both penalized likelihood (PL) and Bayesian methods to create the first dated phylogeny for Salticidae generated with a broad geographic sampling and including fauna from the Afrotropics. The most notable result of the phylogeny concerns the placement of many Central and West African forest species into a single clade, which I informally name the thiratoscirtines. I identify a large Afro-Eurasian clade that includes the Aelurilloida, Plexippoida, the Philaeus group, the Hasarieae/Heliophaninae clade and the Leptorchesteae (APPHHL clade). The APPHHL clade may also include the Euophryinae. The region specific nature of the thiratoscirtine clade supports past studies, which show major salticid groups are confined or mostly confined to Afro-Eurasia, Australasia or the New World. The regional isolation of major salticid clades is concordant with my dating analysis, which shows the family evolved in the Eocene, a time when these three regions were isolated from each other. I date the age of Salticidae to be between 55.2 Ma (PL) and 50.1 Ma (Bayesian). At this time the earth was warmer with expanded megathermal forests and diverse with insect herbivores. -
Convergent Evolution of Eye Ultrastructure and Divergent Evolution of Vision-Mediated Predatory Behaviour in Jumping Spiders
doi: 10.1111/j.1420-9101.2007.01335.x Convergent evolution of eye ultrastructure and divergent evolution of vision-mediated predatory behaviour in jumping spiders K. F. SU,* R. MEIER,* R. R. JACKSON, à D. P. HARLAND §&D.LI* *Department of Biological Sciences, National University of Singapore, Singapore School of Biological Sciences, University of Canterbury, Christchurch, New Zealand àInternational Centre of Insect Physiology and Ecology (ICIPE), Thomas Odhiambo Campus, Mbita Point, Kenya §Structural Biology Group, Canesis Network Ltd, Lincoln, New Zealand Keywords: Abstract aggressive mimicry; All jumping spiders have unique, complex eyes with exceptional spatial acuity araneophagy; and some of the most elaborate vision-guided predatory strategies ever eyes; documented for any animal of their size. However, it is only recently that predatory behaviour; phylogenetic techniques have been used to reconstruct the relationships and Salticidae; key evolutionary events within the Salticidae. Here, we used data for 35 Spartaeinae. species and six genes (4.8 kb) for reconstructing the phylogenetic relationships between Spartaeinae, Lyssomaninae and Salticoida. We document a remark- able case of morphological convergence of eye ultrastructure in two clades with divergent predatory behaviour. We, furthermore, find evidence for a stepwise, gradual evolution of a complex predatory strategy. Divergent predatory behaviour ranges from cursorial hunting to building prey-catching webs and araneophagy with web invasion and aggressive mimicry. Web invasion and aggressive mimicry evolved once from an ancestral spartaeine that was already araneophagic and had no difficulty entering webs due to glue immunity. Web invasion and aggressive mimicry was lost once, in Paracyrba, which has replaced one highly specialized predation strategy with another (hunting mosquitoes). -
Diversity and Community Assembly Structure in Canopy Jumping Spiders (Araneae: Salticidae) Across a Land Use Gradient in Jambi, Sumatra
ZENTRUM FÜR BIODIVERSITÄT UND NACHHALTIGE LANDNUTZUNG − CENTRE OF BIODIVERSITY AND SUSTAINABLE LAND USE − Diversity and community assembly structure in canopy jumping spiders (Araneae: Salticidae) across a land use gradient in Jambi, Sumatra Master’s Thesis for achievement of the academic degree "Master of Science" (M.Sc.) in the study program "Biodiversity, Ecology and Evolution" at the Georg-August Universität Göttingen prepared at the Department of Animal Ecology (Scheu) submitted by B.Sc., Junggebauer, André born in Herford Göttingen, March 2020 First reviewer: Prof. Dr. Stefan Scheu Second reviewer: Prof. Dr. Mark Maraun Day of announcement of the Master’s Thesis: 01.10.2019 Day of delivery of the Master’s Thesis: 24.03.2020 Acknowledgments First, I would like to pay my regards to Prof. Dr. Stefan Scheu and Prof. Dr. Mark Maraun for granting me the opportunity to develop my master’s thesis with these fascinating samples. I also want to express my deepest gratitude to my practical supervisor Dr. Jochen Drescher for his invaluable support throughout the formation of this thesis. Further, I must emphasize the efforts of Dr. Ina Schaefer and Dr. Tamara Hartke as their enthusiasm and expertise fundamentally contributed to this study. Additionally, I am grateful for the contributions of Daniel Ramos, Ting-Wen Chen and Garvin Schulz to this study. Lastly, I am taking this opportunity to perpetuate my gratitude to my parents, thank you for making all of this possible. Contents Abstract ..................................................................................................................................... -
Dynamics Underlying Interacting Mechanisms of Sexual Selection
Dynamics underlying interacting mechanisms of sexual selection by Jeffrey Allan Stoltz A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto © Copyright by Jeffrey Allan Stoltz 2010 Dynamics underlying interacting mechanisms of sexual selection Jeffrey Allan Stoltz Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto 2010 Abstract Sexual selection drives the evolution of male morphology, life history, physiology, and behaviour across taxa. Here I examine the mechanisms of sexual selection that arise at various stages in mating interactions to identify congruence or conflict between the traits selected by choice and competition. I first examine plasticity of developing male Australian redback spiders (Latrodectus hasselti) and show that male metabolic rates vary adaptively to facilitate the scramble to reach virgins. Next, I show that females cease sex pheromone production after mating and re-advertise receptivity later in their reproductive season effectively creating two windows in which males may compete. I show that females discriminate against males that do not meet a threshold courtship duration suggesting that courtship is the trait selected through choice. However, male-male competition leads to reductions in courtship effort provided to females. During the first window paternity is split equally if rival males mate in quick succession with a virgin female. However, if the second mating is delayed, there is a strong bias in the paternity of the second male. A delay in the second mating is beneficial to females as it reduces longevity costs of polyandry. However, delays in the initial mating decrease female longevity, likely because of elevated metabolic rates of virgins.