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Insecta: Dermaptera) with a Check·List of Genera and Species
Rec. zool. Surv. India: 97 (Part-I) : 73-100, 1999 ON THE HIGHER CLASSIFICATION OF ANISOLABIDIDAE (INSECTA: DERMAPTERA) WITH A CHECK·LIST OF GENERA AND SPECIES G. K. SRIVASTAVA* Eastern Regional Station, Zoological Survey of Illdia, ShilJollg INTRODUCTION ~akai (1982) pointed out that family name Anisolabi( di)dae Verhoeff, 1902 has priority 6Verl~arcinophoridae Popham, 1965. Similarly the sub family Anisohibi(di)nae Zacher, 1911 baspriority overCarcinophorinae Hincks, 1954. Accordingly the former are used in the present work. A key for the discrimination of various subfamilies is given. The distinctive characters are based on various morphological character, mainly, on the body shape, shape of thoracic tergites, sternites and the male genitalia. It is proposed to erect a new subfamily Placolabidinae for the reception of Plac.:olabis Bey Bienko, 1959 as its type genus. This genus is very distinct from all t.he known genera of Anisolabidinae in having the median posterior prolongation of 8th sternite in males. Is·olaboidinae has been placed under this family by Srivastava (1996) which was transferred under Spongiphoridae (=Labidae) by Steinmann (1990). An attempt is made here to streamline the taxonomic status of various g~nera of AnisQlabidinae by providing akeyfortheirseparation. The main criteria fortheirdiscrilninatioll is based on the relative length of parameres besides its overall shape. The definition of various genera hOas been enlarged. The genera based on the shape of distal iobes and its associated stnlctures such as chiti nons accessory plates, shape and size of virga and the arrangement of teeth on chitinous pad may not prove t~ be stable characters since these vary intraspecifically. -
Taxonomy of Iberian Anisolabididae (Dermaptera)
Acta Zoologica Academiae Scientiarum Hungaricae 63(1), pp. 29–43, 2017 DOI: 10.17109/AZH.63.1.29.2017 TAXONOMY OF IBERIAN ANISOLABIDIDAE (DERMAPTERA) Mario García-París Museo Nacional de Ciencias Naturales, MNCN-CSIC c/José Gutiérrez Abascal, 2, 28006, Madrid. Spain. E-mail: [email protected] An update on the taxonomy and geographic distribution of Iberian Anisolabididae (Der- maptera) is provided. Former catalogues reported in the Iberian Peninsula three genera of Anisolabididae: Aborolabis, Anisolabis, and Euborellia. A revision of 487 specimens of Iberian and North African Anisolabidoidea permit to exclude the genus Aborolabis from the Iberian fauna, the re-assignation of inland Euborellia annulipes Iberian records to Euborellia moesta, and the exclusion of Aborolabis angulifera from Northwestern Africa. Examination of type materials of Aborolabis mordax and Aborolabis cerrobarjai allows to propose the treatment of A. cerrobarjai as a junior synonym of A. mordax. The diagnostic characters of Euborellia his- panica are included within the local variability found in E. moesta. I propose that E. hispanica should be treated as a junior synonym of E. moesta. Key words: earwigs, systematics, Mediterranean region, Spain, Morocco, NW Africa. INTRODUCTION The Iberian fauna of Dermaptera, including Anisolabididae Verhoeff, 1902, has been the subject of diverse revisionary (Bolívar 1876, 1897, Lapeira & Pascual 1980, Herrera Mesa 1980, Bivar de Sousa 1997) and compilatory works (Herrera Mesa 1999). These revisions together with the monograph of the Fauna of France (Albouy & Caussanel 1990) and the on-line information included in Fauna Europaea (Haas 2010), rendered the image of Dermaptera as a well known group in continental western Europe. -
Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence
When the Body Hides the Ancestry: Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence Petr Kocarek1*, Vaclav John2, Pavel Hulva2,3 1 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Ostrava, Czech Republic, 2 Department of Zoology, Faculty of Science, Charles University in Prague, Prague, Czech Republic, 3 Life Science Research Centre, Faculty of Science, University of Ostrava, Ostrava, Czech Republic Abstract Here, we present a study regarding the phylogenetic positions of two enigmatic earwig lineages whose unique phenotypic traits evolved in connection with ectoparasitic relationships with mammals. Extant earwigs (Dermaptera) have traditionally been divided into three suborders: the Hemimerina, Arixeniina, and Forficulina. While the Forficulina are typical, well-known, free-living earwigs, the Hemimerina and Arixeniina are unusual epizoic groups living on molossid bats (Arixeniina) or murid rodents (Hemimerina). The monophyly of both epizoic lineages is well established, but their relationship to the remainder of the Dermaptera is controversial because of their extremely modified morphology with paedomorphic features. We present phylogenetic analyses that include molecular data (18S and 28S ribosomal DNA and histone-3) for both Arixeniina and Hemimerina for the first time. This data set enabled us to apply a rigorous cladistics approach and to test competing hypotheses that were previously scattered in the literature. Our results demonstrate that Arixeniidae and Hemimeridae belong in the dermapteran suborder Neodermaptera, infraorder Epidermaptera, and superfamily Forficuloidea. The results support the sister group relationships of Arixeniidae+Chelisochidae and Hemimeridae+Forficulidae. This study demonstrates the potential for rapid and substantial macroevolutionary changes at the morphological level as related to adaptive evolution, in this case linked to the utilization of a novel trophic niche based on an epizoic life strategy. -
Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee
Biodiversity: the UK Overseas Territories Compiled by S. Oldfield Edited by D. Procter and L.V. Fleming ISBN: 1 86107 502 2 © Copyright Joint Nature Conservation Committee 1999 Illustrations and layout by Barry Larking Cover design Tracey Weeks Printed by CLE Citation. Procter, D., & Fleming, L.V., eds. 1999. Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee. Disclaimer: reference to legislation and convention texts in this document are correct to the best of our knowledge but must not be taken to infer definitive legal obligation. Cover photographs Front cover: Top right: Southern rockhopper penguin Eudyptes chrysocome chrysocome (Richard White/JNCC). The world’s largest concentrations of southern rockhopper penguin are found on the Falkland Islands. Centre left: Down Rope, Pitcairn Island, South Pacific (Deborah Procter/JNCC). The introduced rat population of Pitcairn Island has successfully been eradicated in a programme funded by the UK Government. Centre right: Male Anegada rock iguana Cyclura pinguis (Glen Gerber/FFI). The Anegada rock iguana has been the subject of a successful breeding and re-introduction programme funded by FCO and FFI in collaboration with the National Parks Trust of the British Virgin Islands. Back cover: Black-browed albatross Diomedea melanophris (Richard White/JNCC). Of the global breeding population of black-browed albatross, 80 % is found on the Falkland Islands and 10% on South Georgia. Background image on front and back cover: Shoal of fish (Charles Sheppard/Warwick -
Striped Earwig
Beneficial Species Profile Photo credit: Joseph Berger, Bugwood.org Common Name: Striped Earwig Scientific Name: Labidura riparia Order and Family: Dermaptera: Labiduridae Size and Appearance: A small, mostly soft-bodied insect that appears pale brown in color with two lengthwise stripes on the pronotum, which is the protective outer plate covering the insect’s thorax. Front wings appear to be shortened and disguise much longer hind wings folded up beneath. Large pincher-like cerci, which are paired appendages at the end of the abdomen. Male cerci are widely separated at the base, slightly curved, and symmetrical. Antenna have 14-24 segments; 4th, 5th & 6th antennae segments combined are shorter than the 1st segment. 2nd tarsal segment is cylindrical, not lobed. Length (mm) Appearance Egg ~ 1mm but can swell to over Pearly grayish-white; laid in clustered double the size while uptaking masses water during development Larva/Nymph Strongly resemble the adult without 2mm- 18mm developed wings; whitish appearance when first born; 4 instars Adult Pale brown in color; front wings appear to be shortened and disguise much 18-26mm longer hind wings folded up beneath; Large pincher-like cerci on abdomen; antennae have 14-24 segments; 4th, 5th & 6th antennae segments combined are shorter than the 1st segment. 2nd tarsal segment is cylindrical, not lobed. Pupa (if applicable) Incomplete Metamorphosis (no pupae) n/a Type of feeder (Chewing, sucking, etc.): Chewing mouthparts on adult and immature. Host/s: Widespread and found on a variety of hosts in all life cycles including, but not limited to, ground litter, beaches, river banks, and irrigation fields. -
A Synergism Between Dimethyl Trisulfide and Methyl Thiolacetate
University of Connecticut OpenCommons@UConn Department of Ecology and Evolutionary EEB Articles Biology 2020 A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically-Supplemented Minimal Trap Stephen T. Trumbo University of Connecticut at Waterbury, [email protected] John Dicapua III University of Connecticut at Waterbury, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/eeb_articles Part of the Behavior and Ethology Commons, and the Entomology Commons Recommended Citation Trumbo, Stephen T. and Dicapua, John III, "A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically- Supplemented Minimal Trap" (2020). EEB Articles. 46. https://opencommons.uconn.edu/eeb_articles/46 1 1 2 A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting 3 Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically-Supplemented 4 Minimal Trap 5 6 Stephen T. Trumbo* and John A. Dicapua III 7 8 University of Connecticut, Department of Ecology and Evolutionary Biology, 9 Waterbury, Connecticut, USA 10 11 *Department of Ecology and Evolutionary Biology, University of Connecticut, 99 E. 12 Main St., Waterbury, CT 06710, U.S.A. ([email protected]) 13 ORCID - 0000-0002-4455-4211 14 15 Acknowledgements 16 We thank Alfred Newton (staphylinids), Armin MocZek and Anna Macagno (scarabs) 17 for their assistance with insect identification. Sandra Steiger kindly reviewed the 18 manuscript. The Southern Connecticut Regional Water Authority and the Flanders 19 Preserve granted permission for field experiments. The research was supported by 20 the University of Connecticut Research Foundation. -
(Insecta: Dermaptera) with a Check-List of Genera and Species
Rec. zool. Surv. India: 97 (Part-I) : 73-100, 1999 ON THE HIGHER CLASSIFICATION OF ANISOLABIDIDAE (INSECTA: DERMAPTERA) WITH A CHECK·LIST OF GENERA AND SPECIES G. K. SRIVASTAVA* Eastern Regional Station, Zoological Survey of Illdia, ShilJollg INTRODUCTION ~akai (1982) pointed out that family name Anisolabi( di)dae Verhoeff, 1902 has priority 6Verl~arcinophoridae Popham, 1965. Similarly the sub family Anisohibi(di)nae Zacher, 1911 baspriority overCarcinophorinae Hincks, 1954. Accordingly the former are used in the present work. A key for the discrimination of various subfamilies is given. The distinctive characters are based on various morphological character, mainly, on the body shape, shape of thoracic tergites, sternites and the male genitalia. It is proposed to erect a new subfamily Placolabidinae for the reception of Plac.:olabis Bey Bienko, 1959 as its type genus. This genus is very distinct from all t.he known genera of Anisolabidinae in having the median posterior prolongation of 8th sternite in males. Is·olaboidinae has been placed under this family by Srivastava (1996) which was transferred under Spongiphoridae (=Labidae) by Steinmann (1990). An attempt is made here to streamline the taxonomic status of various g~nera of AnisQlabidinae by providing akeyfortheirseparation. The main criteria fortheirdiscrilninatioll is based on the relative length of parameres besides its overall shape. The definition of various genera hOas been enlarged. The genera based on the shape of distal iobes and its associated stnlctures such as chiti nons accessory plates, shape and size of virga and the arrangement of teeth on chitinous pad may not prove t~ be stable characters since these vary intraspecifically. -
Big Wigs and Small Wigs: the Roles of Size, Sex and Shelter in Spatial Distribution Patterns in the Maritime Earwig Anisolabis Maritima
Big wigs and small wigs: the roles of size, sex and shelter in spatial distribution patterns in the maritime earwig Anisolabis maritima Nicole Hack1,2, Vikram Iyengar¹,3 Blinks/NSF REU/BEACON 2013 Summer 2013 Contact Information: Nicole Hack Ecology and Evolutionary Biology Department University of California Santa Cruz 1156 High St. Santa Cruz, CA 95064 [email protected] Keywords: Anisolabis maritima, maritime earwig, cohabitation, sex and size 1 Friday Harbor Laboratories, University of Washington, Friday Harbor, Washington 98250 2 Department of Ecology and Evolutionary Biology, University of California Santa Cruz, Santa Cruz, CA 95064 3 Department of Biology, Villanova University, Villanova, PA 19085 Hack 1 Abstract Animal aggregations can occur for a variety of abiotic factors, such as resource limitation, or biotic factors including sexual selection and predator-prey interactions. Although it is challenging to determine the underlying mechanism of such grouping behavior, we conducted experiments in which we examined the interactions and distribution patterns among pairs of the maritime earwig Anisolabis maritima (Order Dermaptera). This insect, found in aggregations under beach debris around the world, is sexually dimorphic regarding its most distinctive feature in that females have straight posterior forceps/pinchers whereas males have asymmetrical, curved forceps. We placed pairs of individuals varying in sex and size and monitored their distribution with and without shelter at 15 min, 12 h and 24 h to determine the roles that these factors may play in spatial patterns and gain insight into the mating system. Overall, we found that females were less likely to cohabitate than males, and they were more tolerant of males than other females. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
Earwigs from Brazilian Caves, with Notes on the Taxonomic and Nomenclatural Problems of the Dermaptera (Insecta)
A peer-reviewed open-access journal ZooKeys 713: 25–52 (2017) Cave-dwelling earwigs of Brazil 25 doi: 10.3897/zookeys.713.15118 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Earwigs from Brazilian caves, with notes on the taxonomic and nomenclatural problems of the Dermaptera (Insecta) Yoshitaka Kamimura1, Rodrigo L. Ferreira2 1 Department of Biology, Keio University, 4-1-1 Hiyoshi, Yokohama 223-8521, Japan 2 Center of Studies in Subterranean Biology, Biology Department, Federal University of Lavras, CEP 37200-000 Lavras (MG), Brazil Corresponding author: Yoshitaka Kamimura ([email protected]) Academic editor: Y. Mutafchiev | Received 17 July 2017 | Accepted 19 September 2017 | Published 2 November 2017 http://zoobank.org/1552B2A9-DC99-4845-92CF-E68920C8427E Citation: Kamimura Y, Ferreira RL (2017) Earwigs from Brazilian caves, with notes on the taxonomic and nomenclatural problems of the Dermaptera (Insecta). ZooKeys 713: 25–52. https://doi.org/10.3897/zookeys.713.15118 Abstract Based on samples collected during surveys of Brazilian cave fauna, seven earwig species are reported: Cy- lindrogaster cavernicola Kamimura, sp. n., Cylindrogaster sp. 1, Cylindrogaster sp. 2, Euborellia janeirensis, Euborellia brasiliensis, Paralabellula dorsalis, and Doru luteipes, as well as four species identified to the (sub) family level. To date, C. cavernicola Kamimura, sp. n. has been recorded only from cave habitats (but near entrances), whereas the other four organisms identified at the species level have also been recorded from non-cave habitats. Wings and female genital structures of Cylindrogaster spp. (Cylindrogastrinae) are examined for the first time. The genital traits, including the gonapophyses of the 8th abdominal segment shorter than those of the 9th segement, and venation of the hind wings of Cylindrogastrinae correspond to those of the members of Diplatyidae and not to Pygidicranidae. -
Alteration of Gut Microbiota with a Broad-Spectrum Antibiotic Does Not Impair Maternal Care in the European Earwig
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.08.331363; this version posted February 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Alteration of gut microbiota with a broad-spectrum antibiotic does not impair 2 maternal care in the European earwig. 3 Sophie Van Meyel*, Séverine Devers, Simon Dupont, Franck Dedeine and Joël Meunier 4 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261 CNRS – Université de Tours, Tours, 5 France 6 *Corresponding author: S. Van Meyel, [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2020.10.08.331363; this version posted February 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. ABSTRACT 7 The microbes residing within the gut of an animal host often increase their own fitness by 8 modifying their host’s physiological, reproductive, and behavioural functions. Whereas recent 9 studies suggest that they may also shape host sociality and therefore have critical effects on 10 animal social evolution, the impact of the gut microbiota on maternal care remains unexplored. 11 This is surprising, as this behaviour is widespread among animals, often determines the fitness 12 of both juveniles and parents, and is essential in the evolution of complex animal societies.