A Taxonomic Review of the Trapdoor Spider Genus Myrmekiaphila (Araneae, Mygalomorphae, Cyrtaucheniidae)
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On the Spider Genus Rhoicinus (Araneae, Trechaleidae) in a Central Amazonian Inundation Fores T
1994. The Journal of Arachnology 22 :54—59 ON THE SPIDER GENUS RHOICINUS (ARANEAE, TRECHALEIDAE) IN A CENTRAL AMAZONIAN INUNDATION FORES T Hubert Hofer: Staatliches Museum fair Naturkunde, Erbprinzenstr . 13, 7613 3 Karlsruhe, Germany Antonio D. Brescovit: Museu de Ciencias Naturais, Fundacdo Zoobotanica do Rio Grande do Sul, C . P. 1188, 90 .001-970 Porto Alegre, Brazil ABSTRACT. The male of Rhoicinus gaujoni Simon and the new species Rhoicinus lugato are described. They co-occur in a whitewater-inundation forest in central Amazonia, Brazil, but were not found in a nearby, inten- sively studied blackwater-inundation forest . Rhoicinus gaujoni builds complex, irregular sheet webs on the ground with a silk tube as a retreat . This report enlarges the distribution of the genus from western Sout h America to the central Amazon basin . The spider genus Rhoicinus was proposed by uated on Ilha de Marchantaria (3°15'S, 59°58'W) , Simon (1898a), based on the type species R. gau- the first island in the Solimoes-Amazon river , joni, from Ecuador. Exline (1950, 1960) de- approximately 15 km above its confluence wit h scribed five new species in the genus, R. wallsi the Rio Negro . The forest is annually flooded from Ecuador and R. rothi, R. schlingeri, R . an- between February and September to a depth o f dinus, R. weyrauchi, all from Peru . The genus 3—5 m. The region is subject to a rainy season was placed in the Amaurobiidae by Lehtinen (December to May) and a dry season (June to (1967), followed by Platnick (1989) in his cata- November). -
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Bull. Br. arachnol. Soc. (1998) 11 (2), 73-80 73 Possible links between embryology, lack of & Pereira, 1995; Eberhard & Huber, in press a), Cole- innervation, and the evolution of male genitalia in optera (Peschke, 1978; Eberhard, 1993a,b; Krell, 1996; Eberhard & Kariko, 1996), Homoptera (Kunze, 1957), spiders Hemiptera (Bonhag & Wick, 1953; Heming-Battum & Heming, 1986, 1989), and Hymenoptera (Roig-Alsina, William G. Eberhard 1993) (see also Snodgrass, 1935 on insects in general, Smithsonian Tropical Research Institute, and and Tadler, 1993, 1996 on millipedes). Escuela de Biología, Universidad de Costa Rica, Ciudad Universitaria, Costa Rica It is of course difficult to present quantitative data on these points, and there are obviously exceptions to and these general statements. For example, in spiders although male pholcid genitalia have elaborate internal Bernhard A. Huber locking and bracing devices (partly in relation to the Escuela de Biología, Universidad de Costa Rica, chelicerae), most or all of the genital structures of the Ciudad Universitaria, Costa Rica* female that are contacted by the male genitalia are membranous (Uhl et al., 1995; Huber, 1994a, 1995c; Summary Huber & Eberhard, 1997). Some portions of the female sperm-receiving organs are also soft in the tetragnathids The male genitalia of spiders apparently lack innervation, Nephila and Leucauge (Higgins, 1989; Eberhard & probably because they are derived embryologically from Huber, in press b), as are the female genital structures structures that secrete the tarsal claw, a structure which lacks nerves. The resultant lack of both sensation and fine that guide the male’s embolus in Histopona torpida muscular control in male genitalia may be responsible for (C. -
Description of a Novel Mating Plug Mechanism in Spiders and the Description of the New Species Maeota Setastrobilaris (Araneae, Salticidae)
A peer-reviewed open-access journal ZooKeys 509: 1–12Description (2015) of a novel mating plug mechanism in spiders and the description... 1 doi: 10.3897/zookeys.509.9711 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Description of a novel mating plug mechanism in spiders and the description of the new species Maeota setastrobilaris (Araneae, Salticidae) Uriel Garcilazo-Cruz1, Fernando Alvarez-Padilla1 1 Laboratorio de Aracnología. Facultad de Ciencias, Universidad Nacional Autonoma de Mexico s/n Ciudad Universitaria, México D. F. Del. Coyoacán, Código postal 04510, México Corresponding author: Fernando Alvarez-Padilla ([email protected]) Academic editor: D. Dimitrov | Received 27 March 2015 | Accepted 5 June 2015 | Published 22 June 2015 http://zoobank.org/A9EA00BB-C5F4-4F2A-AC58-5CF879793EA0 Citation: Garcilazo-Cruz U, Alvarez-Padilla F (2015) Description of a novel mating plug mechanism in spiders and the description of the new species Maeota setastrobilaris (Araneae, Salticidae). ZooKeys 509: 1–12. doi: 10.3897/ zookeys.509.9711 Abstract Reproduction in arthropods is an interesting area of research where intrasexual and intersexual mecha- nisms have evolved structures with several functions. The mating plugs usually produced by males are good examples of these structures where the main function is to obstruct the female genitalia against new sperm depositions. In spiders several types of mating plugs have been documented, the most common ones include solidified secretions, parts of the bulb or in some extraordinary cases the mutilation of the entire palpal bulb. Here, we describe the first case of modified setae, which are located on the cymbial dorsal base, used directly as a mating plug for the Order Araneae in the species Maeota setastrobilaris sp. -
Introduction to Arthropod Groups What Is Entomology?
Entomology 340 Introduction to Arthropod Groups What is Entomology? The study of insects (and their near relatives). Species Diversity PLANTS INSECTS OTHER ANIMALS OTHER ARTHROPODS How many kinds of insects are there in the world? • 1,000,0001,000,000 speciesspecies knownknown Possibly 3,000,000 unidentified species Insects & Relatives 100,000 species in N America 1,000 in a typical backyard Mostly beneficial or harmless Pollination Food for birds and fish Produce honey, wax, shellac, silk Less than 3% are pests Destroy food crops, ornamentals Attack humans and pets Transmit disease Classification of Japanese Beetle Kingdom Animalia Phylum Arthropoda Class Insecta Order Coleoptera Family Scarabaeidae Genus Popillia Species japonica Arthropoda (jointed foot) Arachnida -Spiders, Ticks, Mites, Scorpions Xiphosura -Horseshoe crabs Crustacea -Sowbugs, Pillbugs, Crabs, Shrimp Diplopoda - Millipedes Chilopoda - Centipedes Symphyla - Symphylans Insecta - Insects Shared Characteristics of Phylum Arthropoda - Segmented bodies are arranged into regions, called tagmata (in insects = head, thorax, abdomen). - Paired appendages (e.g., legs, antennae) are jointed. - Posess chitinous exoskeletion that must be shed during growth. - Have bilateral symmetry. - Nervous system is ventral (belly) and the circulatory system is open and dorsal (back). Arthropod Groups Mouthpart characteristics are divided arthropods into two large groups •Chelicerates (Scissors-like) •Mandibulates (Pliers-like) Arthropod Groups Chelicerate Arachnida -Spiders, -
Psalmopoeus Cambridgei (Trinidad Chevron Tarantula)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Psalmopoeus cambridgei (Trinidad Chevron Tarantula) Order: Araneae (Spiders) Class: Arachnida (Spiders and Scorpions) Phylum: Arthropoda (Arthropods) Fig. 1. Trinidad chevron tarantula, Psalmopoeus cambridgei. [http://www.exoreptiles.com/my/index.php?main_page=product_info&products_id=1127, downloaded 30 April 2015] TRAITS. A large spider, maximum size 11-14cm across the legs, with chevrons (V-shaped marks) on the abdomen (Fig. 1). Males are either grey or brown in colour, and females vary from green to brown with red or orange markings on the legs (Wikipedia, 2013). The Trinidad chevron tarantula is hairy in appearance, has eight legs, and its body is divided into two parts, the cephalothorax and the abdomen which are connected by a pedicel that looks like a narrow stalk (Fig. 2). The cephalothorax has eight legs plus a pair of smaller leg-like appendages (pedipalps) used to catch prey; in males these have palpal bulbs attached to the ends for holding sperm (Fig. 3). The mouth has chelicerae with fangs at the ends and swollen bases that house the venom glands, and there are eight small eyes (Foelix, 2010). However, even with eight eyes the Trinidad chevron tarantula can hardly see and so depends mostly on touch, smell, and taste to find its way. There are organs on their feet to detect changes in the environment and special type of hair on their legs and pedipalps for taste. The second part, the abdomen attached to a narrow waist, can UWI The Online Guide to the Animals of Trinidad and Tobago Ecology expand and contract to accommodate food and eggs; two pairs of spinnerets are located at the end of the abdomen (Fig. -
Transcriptome Characterization of the Aptostichus Atomarius Species Complex Nicole L
Garrison et al. BMC Evolutionary Biology (2020) 20:68 https://doi.org/10.1186/s12862-020-01606-7 RESEARCH ARTICLE Open Access Shifting evolutionary sands: transcriptome characterization of the Aptostichus atomarius species complex Nicole L. Garrison1*, Michael S. Brewer2 and Jason E. Bond3 Abstract Background: Mygalomorph spiders represent a diverse, yet understudied lineage for which genomic level data has only recently become accessible through high-throughput genomic and transcriptomic sequencing methods. The Aptostichus atomarius species complex (family Euctenizidae) includes two coastal dune endemic members, each with inland sister species – affording exploration of dune adaptation associated patterns at the transcriptomic level. We apply an RNAseq approach to examine gene family conservation across the species complex and test for patterns of positive selection along branches leading to dune endemic species. Results: An average of ~ 44,000 contigs were assembled for eight spiders representing dune (n = 2), inland (n = 4), and atomarius species complex outgroup taxa (n = 2). Transcriptomes were estimated to be 64% complete on average with 77 spider reference orthologs missing from all taxa. Over 18,000 orthologous gene clusters were identified within the atomarius complex members, > 5000 were detected in all species, and ~ 4700 were shared between species complex members and outgroup Aptostichus species. Gene family analysis with the FUSTr pipeline identified 47 gene families appearing to be under selection in the atomarius ingroup; four of the five top clusters include sequences strongly resembling other arthropod venom peptides. The COATS pipeline identified six gene clusters under positive selection on branches leading to dune species, three of which reflected the preferred species tree. -
Deep Molecular Divergence in the Absence of Morphological And
MEC1233.fm Page 899 Thursday, March 22, 2001 10:50 AM Molecular Ecology (2001) 10, 899–910 DeepBlackwell Science, Ltd molecular divergence in the absence of morphological and ecological change in the Californian coastal dune endemic trapdoor spider Aptostichus simus J. E. BOND,* M. C. HEDIN,† M. G. RAMIREZ‡ and B. D. OPELL§ *Department of Zoology — Insect Division, Field Museum of Natural History, Roosevelt Road at Lake Shore Drive, Chicago, IL 60605 USA, †Department of Biology, San Diego State University, San Diego, CA 92182 – 4614 USA, ‡Department of Biology, Loyola Marymount University, 7900 Loyola Boulevard, Los Angeles, CA 90045 – 8220 USA, §Department of Biology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24060 USA Abstract Aptostichus simus is a trapdoor spider endemic to the coastal dunes of central and southern California and, on morphological grounds, is recognized as a single species. Mitochondrial DNA 16S rRNA sequences demonstrate that most populations are fixed for the same haplo- type and that the population haplotypes from San Diego County, Los Angeles County, Santa Rosa Island, and Monterey County are extremely divergent (6 –12%), with estimated separation times ranging from 2 to 6 million years. A statistical cluster analysis of morpho- logical features demonstrates that this genetic divergence is not reflected in anatomical features that might signify ecological differentiation among these lineages. The species status of these divergent populations of A. simus depends upon the species concept utilized. If a time-limited genealogical perspective is employed, A. simus would be separated at the base into two genetically distinct species. This study suggests that species concepts based on morphological distinctiveness, in spider groups with limited dispersal capabilities, probably underestimate true evolutionary diversity. -
A Summary List of Fossil Spiders
A summary list of fossil spiders compiled by Jason A. Dunlop (Berlin), David Penney (Manchester) & Denise Jekel (Berlin) Suggested citation: Dunlop, J. A., Penney, D. & Jekel, D. 2010. A summary list of fossil spiders. In Platnick, N. I. (ed.) The world spider catalog, version 10.5. American Museum of Natural History, online at http://research.amnh.org/entomology/spiders/catalog/index.html Last udated: 10.12.2009 INTRODUCTION Fossil spiders have not been fully cataloged since Bonnet’s Bibliographia Araneorum and are not included in the current Catalog. Since Bonnet’s time there has been considerable progress in our understanding of the spider fossil record and numerous new taxa have been described. As part of a larger project to catalog the diversity of fossil arachnids and their relatives, our aim here is to offer a summary list of the known fossil spiders in their current systematic position; as a first step towards the eventual goal of combining fossil and Recent data within a single arachnological resource. To integrate our data as smoothly as possible with standards used for living spiders, our list follows the names and sequence of families adopted in the Catalog. For this reason some of the family groupings proposed in Wunderlich’s (2004, 2008) monographs of amber and copal spiders are not reflected here, and we encourage the reader to consult these studies for details and alternative opinions. Extinct families have been inserted in the position which we hope best reflects their probable affinities. Genus and species names were compiled from established lists and cross-referenced against the primary literature. -
Orsolobidae Hickmanolobus
Three new species of the Australian orsolobid spider genus HickmanoloLJus (Araneae: Orsolobidae) Barbara C. Baehr' and Helen M. Smith2 'Queensland Museum, PO.Box 3300, South Brisbane, Queensland 4101, Australia. E-mail: [email protected]. 'Australian Museum, (, College Street, Sydney, New South W,lles 2010, Australia. E-mail: [email protected] Abstract - Three new species of the Australian orsolobid spider genus llicKIIIII/IO!O!JIIS Forster and PI,ltnick 19H5 are described from Queensland and New South \Vales. lficKIIIIIIlO!O!JIIS i!lisCil sI'.. nov., l1iCKlIlilIlO/O!JIIS sI'.. novo and HicKIIlIII/O/O/JlIS lillllilci sI'.. novo are the first l1iCKIlIilIlO!O!liIS species to be described from the mainland of Austrillia. INTRODUCTION stages of 95'1" and 100% ethanol and then critical The tribe Orsolobini Cooke was separated from point drying. SEM's were taken with a Hitachi the Dysderidae by Forster and Platnick (1985), LEO 435VP SEM using a Robinson backscatter who established the family Orsolobidae. With detector. Descriptions were generated with the aid about 180 described species in 28 genera the of the PBI descriptive goblin spider database and Orsolobidae are an important component of the shortened where possible. The map was created forest litter fauna of the southern hemisphere with Biolink version 1.5 (CSIRO Entomology, (Eorster and Forster 1999; Griswold and Platnick Canberra, Australia; http://www.biolink.csiro. 1987; Platnick and Brescovit 1994). To date there au/). All measurements are in millimetres. are only four genera known from Australia. The Throughout the text, figures cited from other most common Australian genus, TOSIIlOIlOOIlOps publications are listed as "figure", those given in liickman 1930, with 29 species, occurs mainly in this paper as "Figure". -
The Phylogeny of Fossil Whip Spiders Russell J
Garwood et al. BMC Evolutionary Biology (2017) 17:105 DOI 10.1186/s12862-017-0931-1 RESEARCH ARTICLE Open Access The phylogeny of fossil whip spiders Russell J. Garwood1,2*, Jason A. Dunlop3, Brian J. Knecht4 and Thomas A. Hegna4 Abstract Background: Arachnids are a highly successful group of land-dwelling arthropods. They are major contributors to modern terrestrial ecosystems, and have a deep evolutionary history. Whip spiders (Arachnida, Amblypygi), are one of the smaller arachnid orders with ca. 190 living species. Here we restudy one of the oldest fossil representatives of the group, Graeophonus anglicus Pocock, 1911 from the Late Carboniferous (Duckmantian, ca. 315 Ma) British Middle Coal Measures of the West Midlands, UK. Using X-ray microtomography, our principal aim was to resolve details of the limbs and mouthparts which would allow us to test whether this fossil belongs in the extant, relict family Paracharontidae; represented today by a single, blind species Paracharon caecus Hansen, 1921. Results: Tomography reveals several novel and significant character states for G. anglicus; most notably in the chelicerae, pedipalps and walking legs. These allowed it to be scored into a phylogenetic analysis together with the recently described Paracharonopsis cambayensis Engel & Grimaldi, 2014 from the Eocene (ca. 52 Ma) Cambay amber, and Kronocharon prendinii Engel & Grimaldi, 2014 from Cretaceous (ca. 99 Ma) Burmese amber. We recovered relationships of the form ((Graeophonus (Paracharonopsis + Paracharon)) + (Charinus (Stygophrynus (Kronocharon (Charon (Musicodamon + Paraphrynus)))))). This tree largely reflects Peter Weygoldt’s 1996 classification with its basic split into Paleoamblypygi and Euamblypygi lineages; we were able to score several of his characters for the first time in fossils. -
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. -
Systematics of the Californian Euctenizine Spider Genus Apomastus
CSIRO PUBLISHING www.publish.csiro.au/journals/is Invertebrate Systematics, 2004, 18, 361–376 Systematics of the Californian euctenizine spider genus Apomastus (Araneae:Mygalomorphae:Cyrtaucheniidae): the relationship between molecular and morphological taxonomy Jason E. Bond East Carolina University, Department of Biology, Howell Science Complex–N211, Greenville, NC 27858, USA. Email: [email protected] Abstract. The genus Apomastus Bond & Opell is a relatively small group of mygalomorph spiders with a limited geographic distribution. Restricted to the Los Angeles Basin, San Juan Mountains, and San Joaquin Hills, Apomastus occupies a fragile habitat rapidly succumbing to urban encroachment. Although originally described as monotypic, the genus was hypothesised to contain at least one additional species. However, females of the two reputed species are morphologically indistinguishable and the authors were unable confidently to assign specific status to populations for which they lacked male specimens. Using an approach that combines geographic, morphological and molecular data, all known populations are assigned to one of two hypothesised species. Mitochondrial DNA cytochrome c oxidase I sequences are used to infer population phylogeny, providing the evolutionary framework necessary to resolve population and species identity issues. Conflicts between the parsimony and Bayesian analyses raise questions about species delineation, species paraphyly, and the application of molecular taxonomy to these taxa. Issues relevant to the conservation of Apomastus species are discussed in light of the substantive intraspecific species divergence observed in the mtDNA data. The type species, Apomastus schlingeri Bond & Opell, is redescribed and a second species, Apomastus kristenae, sp. nov., is described. Additional keywords: conservation genetics, cytochrome oxidase, molecular systematics, molecular taxonomy, phylogeography, species paraphyly, spider taxonomy.