Integrating and Visualising Primary Data from Prospective and Legacy Taxonomic Literature
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A Checklist of the Non -Acarine Arachnids
Original Research A CHECKLIST OF THE NON -A C A RINE A R A CHNIDS (CHELICER A T A : AR A CHNID A ) OF THE DE HOOP NA TURE RESERVE , WESTERN CA PE PROVINCE , SOUTH AFRIC A Authors: ABSTRACT Charles R. Haddad1 As part of the South African National Survey of Arachnida (SANSA) in conserved areas, arachnids Ansie S. Dippenaar- were collected in the De Hoop Nature Reserve in the Western Cape Province, South Africa. The Schoeman2 survey was carried out between 1999 and 2007, and consisted of five intensive surveys between Affiliations: two and 12 days in duration. Arachnids were sampled in five broad habitat types, namely fynbos, 1Department of Zoology & wetlands, i.e. De Hoop Vlei, Eucalyptus plantations at Potberg and Cupido’s Kraal, coastal dunes Entomology University of near Koppie Alleen and the intertidal zone at Koppie Alleen. A total of 274 species representing the Free State, five orders, 65 families and 191 determined genera were collected, of which spiders (Araneae) South Africa were the dominant taxon (252 spp., 174 genera, 53 families). The most species rich families collected were the Salticidae (32 spp.), Thomisidae (26 spp.), Gnaphosidae (21 spp.), Araneidae (18 2 Biosystematics: spp.), Theridiidae (16 spp.) and Corinnidae (15 spp.). Notes are provided on the most commonly Arachnology collected arachnids in each habitat. ARC - Plant Protection Research Institute Conservation implications: This study provides valuable baseline data on arachnids conserved South Africa in De Hoop Nature Reserve, which can be used for future assessments of habitat transformation, 2Department of Zoology & alien invasive species and climate change on arachnid biodiversity. -
An In-Depth Biochemical Analysis of Spider and Silkworm Silk
Unravelling the secrets of silk: an in-depth biochemical analysis of spider and silkworm silk Hamish Cameron Craig A thesis in fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological, Earth and Environmental Sciences Evolution and Ecology Research Centre UNSW February 2019 THE UNIVERSITY OF NEW SOUTH WALES Thesis/Dissertation Sheet Surname or Family name: Craig First name: Hamish Other name/s: Cameron Abbreviation for degree as given in the University calendar: PhD School: School of Biological, Earth and Environmental Sciences Faculty: Faculty of Science Title: Unravelling the secrets of silk: a detailed examination of silk biology and structure Abstract: Silk is a protein-based biopolymer produced by many different invertebrate species from amphipods to spiders. Its incredible material properties, biocompatibility and antimicrobial properties make it one of the most desirable natural fibres in the race for new materials, with major potential impacts in everything from biomedical research to its aerospace applications. Although silk has been studied in detail since the latter part of the 20th century the field is still unable to produce truly comparable synthetics due to the complexity of biological factors involved in influencing silks properties. The major focus of this thesis is examining biological and structural factors that impact silk properties within spiders and silkworms. To examine this, I analysed silk across many scales from phylogenetic trends in amino acid composition and material properties, down to the Nano-scale examining the impacts of molecular structure, pioneering new methods of silk analysis through utilisation of dynamic nuclear polarization (DNP) solid-state nuclear magnetic resonance (ssNMR) spectroscopy. -
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i/'meI1can %MllselIm Ntats PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, N. Y. I0024 NUMBER 2292 APRIL 24, I967 Descriptions of the Spider Families Desidae and Argyronetidae BY VINCENT D. ROTH1 The marine spiders of the genus Desis Walckenaer and the Eurasian water spider Argyroneta aquatica (Clerck) have been considered by most arachnologists to be aberrant members of the family Agelenidae. The family Desidae was established in 1895 for Desis but since has been ignored. The family Argyronetidae, proposed in 1870, has been used as follows: exclusively for the genus Argyroneta Latreille; for Argyroneta and certain genera of cybaeinids as an expanded family; and for Argyroneta and the entire agelenid subfamily Cybaeinae. None of the revisers offered adequate reasons for his placement of the genera in the family Argyro- netidae. The present study was initiated because of the uncertain status of Desis and Argyroneta and the lack of published evidence supporting place- ment of them. As a result, I herein propose that each again be elevated to family status. The remaining genera previously associated with the family Argyronetidae belong to the subfamily Cybaeinae of the family Agelenidae (see Roth, 1967a, p. 302, for a description of the family). The differences among the three families of spiders are listed in table 1. 1 Resident Director, Southwestern Research Station of the American Museum of Natural History, Portal, Arizona. 0~~~~ 0.) 0Cc S- c .)00 0 0n Cd C~~~~~~~~~~~~~~~~~~~~~.) 0~~~~ C- 0.) 4 C0 U, 0~ z-o0 ID -~~~~0c - 4 Z 4.) 0 bID D < < ~~~~ 0~~C0.) -o C~~~~..4 C .0 v C bID ~~~"0 0 ~ 0 d 4-'.~~~~~4 + + 2 O 4.) ID 2 0 10 u0r 0 -o 6U 4- 4. -
Volume 73, Number
New Zealand Science Review Vol 73 (3–4) 2016 Symposium on Systematics and Biodiversity in honour of Dr Dennis P. Gordon Official Journal of the New Zealand Association of Scientists ISSN 0028-8667 New Zealand Science Review Vol 73 (3–4) 2016 Official Journal of the New Zealand Association of Scientists P O Box 1874, Wellington www.scientists.org.nz A forum for the exchange of views on science and science policy Managing Editor: Allen Petrey Contents Guest Editor: Daniel Leduc Production Editor: Geoff Gregory Editorial .....................................................................................................................................................61 Proceedings of a Symposium on Systematics and Biodiversity: Past, Present and Future, National Institute of Water & Atmospheric Research, Wellington, April 2016 Bryozoa—not a minor phylum – Dennis P. Gordon and Mark J. Costello ..................................................63 The contribution of Dennis P. Gordon to the understanding of New Zealand Bryozoa – Abigail M Smith, Philip Bock and Peter Batson ................................................................................67 The study of taxonomy and systematics enhances ecological and conservation science – Ashley A. Rowden ............................................................................................................................72 Taxonomic research, collections and associated databases – and the changing science scene in New Zealand – Wendy Nelson .............................................................................79 -
Redescription and Generic Placement of the Spider Cryptachaea
Zootaxa 3507: 38–56 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2012 · Magnolia Press Article ISSN 1175-5334 (online edition) urn:lsid:zoobank.org:pub:8EDE33EB-3C43-4DFA-A1F4-5CC86DED76C8 Redescription and generic placement of the spider Cryptachaea gigantipes (Keyserling, 1890) (Araneae: Theridiidae) and notes on related synanthropic species in Australasia HELEN M. SMITH1,5, COR J. VINK2,3, BRIAN M. FITZGERALD4 & PHIL J. SIRVID4 1 Australian Museum, 6 College St, Sydney, New South Wales 2010, Australia. E-mail: [email protected] 2 Biosecurity & Biocontrol, AgResearch, Private Bag 4749, Christchurch 8140, New Zealand. E-mail: [email protected] 3 Entomology Research Museum, PO Box 84, Lincoln University, Lincoln 7647, New Zealand. 4 Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington 6140, New Zealand. E-mail: [email protected], [email protected] 5 Corresponding author Abstract Cryptachaea gigantipes (Keyserling, 1890) n. comb. is redescribed from fresh material, the female is described for the first time and notes on biology are given. Cryptachaea gigantipes has been recorded from natural habitats in south-eastern Australia, but is also commonly encountered around houses and other built structures, there and in the North Island of New Zealand. The earliest New Zealand records are from the year 2000 and it would appear that the species has been accidentally introduced due to its synanthropic tendencies. The idea of a recent and limited initial introduction is supported by cytochrome c oxidase subunit 1 (COI) sequences, which are extremely homogeneous from New Zealand specimens compared to those from Australia. -
Redescriptions of Nuisiana Arboris (Marples 1959) and Cambridgea Reinga Forster & Wilton 1973 (Araneae: Desidae, Stiphidiidae)
Zootaxa 2739: 41–50 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Reuniting males and females: redescriptions of Nuisiana arboris (Marples 1959) and Cambridgea reinga Forster & Wilton 1973 (Araneae: Desidae, Stiphidiidae) COR J. VINK1,2,5, BRIAN M. FITZGERALD3, PHIL J. SIRVID3 & NADINE DUPÉRRÉ4 1Biosecurity Group, AgResearch, Private Bag 4749, Christchurch 8140, New Zealand. E-mail: [email protected] 2Entomology Research Museum, PO Box 84, Lincoln University, Lincoln 7647, New Zealand. 3Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington 6140, New Zealand. E-mail: [email protected], [email protected] 4Division of Invertebrate Zoology, American Museum of Natural History, Central Park West at 79th Street, New York New York 10024, U.S.A. E-mail: [email protected] 5Corresponding author Abstract Two New Zealand endemic spider species, Nuisiana arboris (Marples 1959) (Desidae) and Cambridgea reinga Forster & Wilton 1973 (Stiphidiidae), are redescribed, including notes on their distribution and DNA sequences from the mitochon- drial gene cytochrome c oxidase subunit 1. Based on morphological evidence and mitochondrial DNA sequences, Mata- chia magna Forster 1970 is a junior synonym of Nuisiana arboris, and Nanocambridgea grandis Blest & Vink 2000 is a junior synonym of Cambridgea reinga. Two forms of male morph in C. reinga are recorded. Key words: cytochrome c oxidase subunit 1 (COI), DNA, Matachia, new synonymy, New Zealand, Nanocambridgea Introduction New Zealand’s spider fauna is diverse with an estimated 1990 species, of which 93% are endemic (Paquin et al. 2010). Most of the 1126 named species were described during the last 60 years and about 60% were described by one man, Ray Forster (Patrick et al. -
Spiders (Araneae) of Churchill, Manitoba: DNA Barcodes And
Blagoev et al. BMC Ecology 2013, 13:44 http://www.biomedcentral.com/1472-6785/13/44 RESEARCH ARTICLE Open Access Spiders (Araneae) of Churchill, Manitoba: DNA barcodes and morphology reveal high species diversity and new Canadian records Gergin A Blagoev1*, Nadya I Nikolova1, Crystal N Sobel1, Paul DN Hebert1,2 and Sarah J Adamowicz1,2 Abstract Background: Arctic ecosystems, especially those near transition zones, are expected to be strongly impacted by climate change. Because it is positioned on the ecotone between tundra and boreal forest, the Churchill area is a strategic locality for the analysis of shifts in faunal composition. This fact has motivated the effort to develop a comprehensive biodiversity inventory for the Churchill region by coupling DNA barcoding with morphological studies. The present study represents one element of this effort; it focuses on analysis of the spider fauna at Churchill. Results: 198 species were detected among 2704 spiders analyzed, tripling the count for the Churchill region. Estimates of overall diversity suggest that another 10–20 species await detection. Most species displayed little intraspecific sequence variation (maximum <1%) in the barcode region of the cytochrome c oxidase subunit I (COI) gene, but four species showed considerably higher values (maximum = 4.1-6.2%), suggesting cryptic species. All recognized species possessed a distinct haplotype array at COI with nearest-neighbour interspecific distances averaging 8.57%. Three species new to Canada were detected: Robertus lyrifer (Theridiidae), Baryphyma trifrons (Linyphiidae), and Satilatlas monticola (Linyphiidae). The first two species may represent human-mediated introductions linked to the port in Churchill, but the other species represents a range extension from the USA. -
Surface-Active Spiders (Araneae) in Ley and Field Margins
Norw. J. Entomol. 51, 57–66. 2004 Surface-active spiders (Araneae) in ley and field margins Reidun Pommeresche Pommeresche, R. 2004. Surface-active spiders (Araneae) in ley and field margins. Norw. J. Entomol. 51, 57-66. Surface-active spiders were sampled from a ley and two adjacent field margins on a dairy farm in western Norway, using pitfall traps from April to June 2001. Altogether, 1153 specimens, represent- ing 33 species, were found. In total, 10 species were found in the ley, 16 species in the edge of the ley, 22 species in the field margin “ley/forest” and 16 species in the field margin “ley/stream”. Erigone atra, Bathyphantes gracilis, Savignia frontata and Collinsia inerrans were the most abun- dant species in the ley. C. inerrans was not found in the field margins. This species is previously recorded only a few times in Norway. Diplocephalus latifrons, Tapinocyba insecta, Dicymbium tibiale, Bathyphantes nigrinus and Diplostyla concolor were most abundant in the field margin “ley/ forest”. D. latifrons, D. tibiale and Pardosa amentata were most abundant in the field margin “ley/ stream”, followed by E. atra and B. gracilis. The present results were compared to results from ley and pasture on another farm in the region, recorded in 2000. A Detrended Correspondence Analyses (DCA) of the data sets showed that the spider fauna from the leys were more similar, independent of location, than the fauna in ley and field margins on the same locality. The interactions between cultivated fields and field margins according to spider species composition, dominance pattern and habitat preferences are discussed. -
A Protocol for Online Documentation of Spider Biodiversity Inventories Applied to a Mexican Tropical Wet Forest (Araneae, Araneomorphae)
Zootaxa 4722 (3): 241–269 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2020 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4722.3.2 http://zoobank.org/urn:lsid:zoobank.org:pub:6AC6E70B-6E6A-4D46-9C8A-2260B929E471 A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae) FERNANDO ÁLVAREZ-PADILLA1, 2, M. ANTONIO GALÁN-SÁNCHEZ1 & F. JAVIER SALGUEIRO- SEPÚLVEDA1 1Laboratorio de Aracnología, Facultad de Ciencias, Departamento de Biología Comparada, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Colonia Copilco el Bajo. C. P. 04510. Del. Coyoacán, Ciudad de México, México. E-mail: [email protected] 2Corresponding author Abstract Spider community inventories have relatively well-established standardized collecting protocols. Such protocols set rules for the orderly acquisition of samples to estimate community parameters and to establish comparisons between areas. These methods have been tested worldwide, providing useful data for inventory planning and optimal sampling allocation efforts. The taxonomic counterpart of biodiversity inventories has received considerably less attention. Species lists and their relative abundances are the only link between the community parameters resulting from a biotic inventory and the biology of the species that live there. However, this connection is lost or speculative at best for species only partially identified (e. g., to genus but not to species). This link is particularly important for diverse tropical regions were many taxa are undescribed or little known such as spiders. One approach to this problem has been the development of biodiversity inventory websites that document the morphology of the species with digital images organized as standard views. -
19 4 273 282 Tanasevitch2 for Inet.P65
Arthropoda Selecta 19(4): 273282 © ARTHROPODA SELECTA, 2010 On synonymy of linyphiid spiders of the Russian fauna (Arachnida: Aranei: Linyphiidae). 1 Î ñèíîíèìèè ïàóêîâ-ëèíèôèèä ôàóíû Ðîññèè (Arachnida: Aranei: Linyphiidae). 1 Andrei V. Tanasevitch À.Â. Òàíàñåâè÷ Centre for Forest Ecology and Production, Russian Academy of Sciences, Profsoyuznaya Str. 84/32, Moscow 117997 Russia. E-mail: and- [email protected] Öåíòð ïî ïðîáëåìàì ýêîëîãèè è ïðîäóêòèâíîñòè ëåñîâ ÐÀÍ, Ïðîôñîþçíàÿ óë. 84/32, Ìîñêâà 117997 Ðîññèÿ. E-mail: and- [email protected] KEY WORDS: Spiders, Linyphiidae, new synonym, new combination, Russian fauna. ÊËÞ×ÅÂÛÅ ÑËÎÂÀ: Ïàóêè, Linyphiidae, íîâûé ñèíîíèì, íîâàÿ êîìáèíàöèÿ, ôàóíà Ðîññèè. ABSTRACT. Seven new synonyms are established Introduction for the Russian fauna: Agyneta yakutsaxatilis Marusik et Koponen, 2002, syn.n. = Agyneta amersaxatilis Hundreds of new taxa of the linyphiid spiders have Saaristo et Koponen, 1998; Bolyphantes palaeformis been described during the last three decades from the (Tanasevitch, 1989), syn.n. = Bolyphantes bipartitus territory of the former Soviet Union, mainly from the (Tanasevitch, 1989), both comb.n. (ex Lepthyphantes Caucasus, Siberia, the Far East and Central Asia. A Menge, 1866); Epigytholus tuvensis Tanasevitch, 1996, significant progress in the taxonomy of the family syn.n. = Epigytholus kaszabi (Wunderlich, 1995), Linyphiidae, as well as abundant material from various comb.n. (ex Lepthyphantes); Hybauchenidium holmi Palearctic regions which has been recently accumulated, Marusik, 1988, syn.n. = Hybauchenidium aquilonare allow one to not only critically consider some of the (L. Koch, 1879); Poeciloneta yanensis Marusik et Ko- earlier described species and genera but also, in some ponen, 2002, syn.n. = Poeciloneta variegata (Black- cases, to dispel any doubts in their invalidity. -
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. -
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 ................................................................................................................................................