Ecological Considerations for Development of the Wildlife Lake, Castlereagh
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
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 ..................................................................................................................................................................... -
Download Article (PDF)
46 Rec. zool. Sura. India Genus. Acrania Burr, 1915 Distribution: INDIA (Tamil Nadu, Himachal 1915. Acrania Burr. J.R. micro Soc., 1915: 432, 436 (Type Pradesh, West Bengal and Kashmir). Pygidicrana picta Guerin-Meneville) Elsewhere: Pakistan, Uganda and Zaire. 1993. Acrania; Srivastava, Rec. zool. Sura. India, 92(1-4): 44. Remarks : This species is recorded for the first time from Kashmir. 3. Acrania fletcheri (Bharadwaj and Kapoor, 1967) 5. Euborellia annulata (Fabricius, 1793) 1967. Cranopygia jletcheri Bharadwaj and Kapoor, Bull. Ent.,8(2) : 1(0"; India: Meghalaya; Shillong, 5000 1793. Forficula annulata Fabricius, Ent. Syst., II : 4 (sex; ft.) Americae meridionale). 1914. Kalocrania picta (nec.Guerin-Meneville); Burr, Rec. 1867. Anisolabis stali; Scudder, Proc. Boston soc. Nat. Hist., Indian Mus., 8(2): 136 (lO",l~, Kobo). 18: 308. 1993. Acrania jletcheri; Srivastava, Rec. zool. Sura. India, 1910. Borellia stali Burr, Fauna of British India, Dermaptera: 92(1-4): 45. 88. Material examined: INDIA: Manipur: Imphal, Material Examined : INDIA: Chennai, Elliots 16 miles North on Dimapur Road, Alt., 3500 ft., Beach, Radio Station, 10", 18.9.1961. 14.x.1945 (Major M.L. Roonwal). Measurements: (in mm): Male Measurements: (in mm): Male Length of body 10mm Length of body 20 Forceps l.5mm. Length of forceps 5.5 Distribution : INDIA (Kerala, Tamil Nadu, Distribution: INDIA: Meghalaya, (Shillong and Karnataka, Maharashtra, Orissa, West Bengal, Manipur) (Imphal district). Manipur and Lakshadweep islands). Elsewhere: Not yet recorded. Elsewhere: Sri Lanka, Pakistan and China. Remarks : It is reported for the first time from Sub family BRACHYLABIDINAE the state of Manipur. Genus Metisolabis Burr, 1910 Super family ANISOLABOIDEA 1910. -
Spiders of the Hawaiian Islands: Catalog and Bibliography1
Pacific Insects 6 (4) : 665-687 December 30, 1964 SPIDERS OF THE HAWAIIAN ISLANDS: CATALOG AND BIBLIOGRAPHY1 By Theodore W. Suman BISHOP MUSEUM, HONOLULU, HAWAII Abstract: This paper contains a systematic list of species, and the literature references, of the spiders occurring in the Hawaiian Islands. The species total 149 of which 17 are record ed here for the first time. This paper lists the records and literature of the spiders in the Hawaiian Islands. The islands included are Kure, Midway, Laysan, French Frigate Shoal, Kauai, Oahu, Molokai, Lanai, Maui and Hawaii. The only major work dealing with the spiders in the Hawaiian Is. was published 60 years ago in " Fauna Hawaiiensis " by Simon (1900 & 1904). All of the endemic spiders known today, except Pseudanapis aloha Forster, are described in that work which also in cludes a listing of several introduced species. The spider collection available to Simon re presented only a small part of the entire Hawaiian fauna. In all probability, the endemic species are only partly known. Since the appearance of Simon's work, there have been many new records and lists of introduced spiders. The known Hawaiian spider fauna now totals 149 species and 4 subspecies belonging to 21 families and 66 genera. Of this total, 82 species (5596) are believed to be endemic and belong to 10 families and 27 genera including 7 endemic genera. The introduced spe cies total 65 (44^). Two unidentified species placed in indigenous genera comprise the remaining \%. Seventeen species are recorded here for the first time. In the catalog section of this paper, families, genera and species are listed alphabetical ly for convenience. -
FNCV Register of Photos
FNCV Register of photos - natural history (FNCVSlideReg is in Library computer: My computer - Local Disc C - Documents and settings - Library) [Square brackets] - added or updated name Slide number Title Place Date Source Plants SN001-1 Banksia marginata Grampians 1974 001-2 Xanthorrhoea australis Labertouche 17 Nov 1974 001-3 Xanthorrhoea australis Anglesea Oct 1983 001-4 Regeneration after bushfire Anglesea Oct 1983 001-5 Grevillea alpina Bendigo 1975 001-6 Glossodia major / Grevillea alpina Maryborough 19 Oct 1974 001-7 Discarded - out of focus 001-8 [Asteraceae] Anglesea Oct 1983 001-9 Bulbine bulbosa Don Lyndon 001-10 Senecio elegans Don Lyndon 001-11 Scaevola ramosissima (Hairy fan-flower) Don Lyndon 001-12 Brunonia australis (Blue pincushion) Don Lyndon 001-13 Correa alba Don Lyndon 001-14 Correa alba Don Lyndon 001-15 Calocephalus brownii (Cushion bush) Don Lyndon 001-16 Rhagodia baccata [candolleana] (Seaberry saltbush) Don Lyndon 001-17 Lythrum salicaria (Purple loosestrife) Don Lyndon 001-18 Carpobrotus sp. (Pigface in the sun) Don Lyndon 001-19 Rhagodia baccata [candolleana] Inverloch Don Lyndon 001-20 Epacris impressa Don Lyndon 001-21 Leucopogon virgatus (Beard-heath) Don Lyndon 001-22 Stackhousia monogyna (Candles) Don Lyndon 001-23 Correa reflexa (yellow) Don Lyndon 001-24 Prostanthera sp. Don Lyndon Fungi 002-1 Stinkhorn fungus Aseroe rubra Buckety Plains 30/12/1974 Margarey Lester 002-2 Fungi collection: Botany Group excursion Dom Dom Saddle 28 May 1988 002-3 Aleuria aurantia Aug 1966 R&M Jennings Bairnsdale FNC 002-4 -
(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. -
ORTHOPTERA in the Swedish Museum of Natural History
ORTHOPTERA in the Swedish Museum of Natural History As of August 2003 Abisares azurea Sjöstedt Type Acrida turrita Linnaeus, 1758 Abisares viridipennis Burmeister Acridella nasuta Linnaeus, 1758 Ablectia rufescens Sjöstedt Type Acridella pharaonis Klug, 1830 Acanthacris citrina Serville Acridella serrata Thunberg, 1815 Acanthacris elgonensis Sjöstedt Acridium australiensis Sjöstedt Type Acanthacris fulva Sjöstedt Acridium basale Walker Acanthacris gyldenstolpi Sjöstedt Acridium eximia Sjöstedt Type Acanthacris lineata Stoll Acridium irregularis Walker Acanthacris ruficornis Fabricius Acridium irregularis Walker Acanthalobus bispinosus Dalman, 1818 Acridium maculicollis Walker Acanthalobus inornatus Walker, 1871 Acridium meleager Sjöstedt Type Acanthodis aquilina Linnaeus, 1758 Acridium modesta Sjöstedt Type Acanthodis curvidens Stål, 1876 Acridium papuasica Finot Acanthodis longicauda Stål, 1895 Acridium pulchripes Sjöstedt Type Acanthoplus jallae Griffini, 1897 Acridium rubripes Sjöstedt Type Acanthoplus longipes Charpentier, 1845 Acridium rubrispinarum Sjöstedt Type Acanthoproctus militaris White, 1846 Acridium signata Sjöstedt Type Acanthoxia ensator Walker Acridium sjöstedti Uvarov Type Acanthoxia gladiator Westwood Acridium vittata Sjöstedt Type Achurum acridodes Stål, 1873 Acridoderes aequalis Mill. Acicera fusca Thunberg, 1815 Acridoderes crassus Bolivar Acidacris violacea Gerstäcker, 1889 Acridoxena hewaniana Smith, 1865 Acinipe algerica Brunner, 1882 Acridoxena macrocephalus Sjöstedt Acinipe crassicornis Bolivar Acripeza reticulata -
The Cytology of Tasmanian Short-Horned Grasshoppers ( Orthoptera: Acridoidea)
PAP. & PROC. ROY. Soc. TASMANIA. VOL. 86. (15TH SEPTEMBER. 1952.) The Cytology of Tasmanian Short-Horned Grasshoppers ( Orthoptera: Acridoidea) By G. B. SHARMAN Department of Botany, University of Tasmania* WITH 1 PLATE AND 57 TEXT FIGURES SUMMARY The cytology of twenty-six of the twenty-nine species of short-horned grass hoppers (superfamily Acridoidea) recorded from Tasmania is described. Intra specific cytological polymorphism is described in some species. Cytological evidence of phylogenetic relationships has been indicated where possible. INTRODUCTION Mainly because of their large size, and general suitability for cyto logical study the chromosomes of the short-horned grasshoppers (super family Acridoidea) have been the subject of wide research. In the largest and most widely studied family, the Acrididae, early workers (McClung, 1905; Davis, 1908) reported the male number as being uniformly twenty three rod-shaped chromosomes, but Granata (1910) showed that Pam phagus possessed nineteen rod-shaped chromosomes. With few exceptions an XO sex chromosome sy~tem is found. Later work has shown that one group of subfamilies of the Acrididae is characterised by the male diploid number of· nineteen rod-shaped chromosomes, whilst another and larger group is characterised by the male diploid number of twenty-three. These are usually called the ten and twelve chromosome groups, and correspond to the Chasmosacci and Cryptosacci groups of subfamilies (Roberts, 1941). Cytologically the Chasmosacci is a very uniform group as has been shown by Rao (1937) and Powers (1942). The twelve chromosome group, how ever, has some cytological variability. In more than forty genera the characteristic male diploid chromosome number of twenty-three is found (White, 1945) ; but" centric fusions" (White, 1945) have been responsible for lowering the chromosome number of some species, although the characteristic twenty-three arms are still found. -
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). -
Temporal Lags and Overlap in the Diversification of Weevils and Flowering Plants
Temporal lags and overlap in the diversification of weevils and flowering plants Duane D. McKennaa,1, Andrea S. Sequeirab, Adriana E. Marvaldic, and Brian D. Farrella aDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; bDepartment of Biological Sciences, Wellesley College, Wellesley, MA 02481; and cInstituto Argentino de Investigaciones de Zonas Aridas, Consejo Nacional de Investigaciones Científicas y Te´cnicas, C.C. 507, 5500 Mendoza, Argentina Edited by May R. Berenbaum, University of Illinois at Urbana-Champaign, Urbana, IL, and approved March 3, 2009 (received for review October 22, 2008) The extraordinary diversity of herbivorous beetles is usually at- tributed to coevolution with angiosperms. However, the degree and nature of contemporaneity in beetle and angiosperm diversi- fication remain unclear. Here we present a large-scale molecular phylogeny for weevils (herbivorous beetles in the superfamily Curculionoidea), one of the most diverse lineages of insects, based on Ϸ8 kilobases of DNA sequence data from a worldwide sample including all families and subfamilies. Estimated divergence times derived from the combined molecular and fossil data indicate diversification into most families occurred on gymnosperms in the Jurassic, beginning Ϸ166 Ma. Subsequent colonization of early crown-group angiosperms occurred during the Early Cretaceous, but this alone evidently did not lead to an immediate and ma- jor diversification event in weevils. Comparative trends in weevil diversification and angiosperm dominance reveal that massive EVOLUTION diversification began in the mid-Cretaceous (ca. 112.0 to 93.5 Ma), when angiosperms first rose to widespread floristic dominance. These and other evidence suggest a deep and complex history of coevolution between weevils and angiosperms, including codiver- sification, resource tracking, and sequential evolution. -
ACT, Australian Capital Territory
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations.