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Habitat Usage by the Page Springsnail, Pyrgulopsis Morrisoni (Gastropoda: Hydrobiidae), from Central Arizona
THE VELIGER ᭧ CMS, Inc., 2006 The Veliger 48(1):8–16 (June 30, 2006) Habitat Usage by the Page Springsnail, Pyrgulopsis morrisoni (Gastropoda: Hydrobiidae), from Central Arizona MICHAEL A. MARTINEZ* U.S. Fish and Wildlife Service, 2321 W. Royal Palm Rd., Suite 103, Phoenix, Arizona 85021, USA (*Correspondent: mike[email protected]) AND DARRIN M. THOME U.S. Fish and Wildlife Service, 2800 Cottage Way, Rm. W-2605, Sacramento, California 95825, USA Abstract. We measured habitat variables and the occurrence and density of the Page springsnail, Pyrgulopsis mor- risoni (Hershler & Landye, 1988), in the Oak Creek Springs Complex of central Arizona during the spring and summer of 2001. Occurrence and high density of P. morrisoni were associated with gravel and pebble substrates, and absence and low density with silt and sand. Occurrence and high density were also associated with lower levels of dissolved oxygen and low conductivity. Occurrence was further associated with shallower water depths. Water velocity may play an important role in maintaining springsnail habitat by influencing substrate composition and other physico-chemical variables. Our study constitutes the first empirical effort to define P. morrisoni habitat and should be useful in assessing the relative suitability of spring environments for the species. The best approach to manage springsnail habitat is to maintain springs in their natural state. INTRODUCTION & Landye, 1988), is medium-sized relative to other con- geners, 1.8 to 2.9 mm in shell height, endemic to the The role that physico-chemical habitat variables play in Upper Verde River drainage of central Arizona (Williams determining the occurrence and density of aquatic micro- et al., 1985; Hershler & Landye, 1988; Hershler, 1994), invertebrates in spring ecosystems has been poorly stud- with all known populations existing within a complex of ied. -
Diversity of Echinostomes (Digenea: Echinostomatidae) in Their Snail Hosts at High Latitudes
Parasite 28, 59 (2021) Ó C. Pantoja et al., published by EDP Sciences, 2021 https://doi.org/10.1051/parasite/2021054 urn:lsid:zoobank.org:pub:9816A6C3-D479-4E1D-9880-2A7E1DBD2097 Available online at: www.parasite-journal.org RESEARCH ARTICLE OPEN ACCESS Diversity of echinostomes (Digenea: Echinostomatidae) in their snail hosts at high latitudes Camila Pantoja1,2, Anna Faltýnková1,* , Katie O’Dwyer3, Damien Jouet4, Karl Skírnisson5, and Olena Kudlai1,2 1 Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic 2 Institute of Ecology, Nature Research Centre, Akademijos 2, 08412 Vilnius, Lithuania 3 Marine and Freshwater Research Centre, Galway-Mayo Institute of Technology, H91 T8NW, Galway, Ireland 4 BioSpecT EA7506, Faculty of Pharmacy, University of Reims Champagne-Ardenne, 51 rue Cognacq-Jay, 51096 Reims Cedex, France 5 Laboratory of Parasitology, Institute for Experimental Pathology, Keldur, University of Iceland, IS-112 Reykjavík, Iceland Received 26 April 2021, Accepted 24 June 2021, Published online 28 July 2021 Abstract – The biodiversity of freshwater ecosystems globally still leaves much to be discovered, not least in the trematode parasite fauna they support. Echinostome trematode parasites have complex, multiple-host life-cycles, often involving migratory bird definitive hosts, thus leading to widespread distributions. Here, we examined the echinostome diversity in freshwater ecosystems at high latitude locations in Iceland, Finland, Ireland and Alaska (USA). We report 14 echinostome species identified morphologically and molecularly from analyses of nad1 and 28S rDNA sequence data. We found echinostomes parasitising snails of 11 species from the families Lymnaeidae, Planorbidae, Physidae and Valvatidae. -
North American Hydrobiidae (Gastropoda: Rissoacea): Redescription and Systematic Relationships of Tryonia Stimpson, 1865 and Pyrgulopsis Call and Pilsbry, 1886
THE NAUTILUS 101(1):25-32, 1987 Page 25 . North American Hydrobiidae (Gastropoda: Rissoacea): Redescription and Systematic Relationships of Tryonia Stimpson, 1865 and Pyrgulopsis Call and Pilsbry, 1886 Robert Hershler Fred G. Thompson Department of Invertebrate Zoology Florida State Museum National Museum of Natural History University of Florida Smithsonian Institution Gainesville, FL 32611, USA Washington, DC 20560, USA ABSTRACT scribed) in the Southwest. Taylor (1966) placed Tryonia in the Littoridininae Taylor, 1966 on the basis of its Anatomical details are provided for the type species of Tryonia turreted shell and glandular penial lobes. It is clear from Stimpson, 1865, Pyrgulopsis Call and Pilsbry, 1886, Fonteli- cella Gregg and Taylor, 1965, and Microamnicola Gregg and the initial descriptions and subsequent studies illustrat- Taylor, 1965, in an effort to resolve the systematic relationships ing the penis (Russell, 1971: fig. 4; Taylor, 1983:16-25) of these taxa, which represent most of the generic-level groups that Fontelicella and its subgenera, Natricola Gregg and of Hydrobiidae in southwestern North America. Based on these Taylor, 1965 and Microamnicola Gregg and Taylor, 1965 and other data presented either herein or in the literature, belong to the Nymphophilinae Taylor, 1966 (see Hyalopyrgus Thompson, 1968 is assigned to Tryonia; and Thompson, 1979). While the type species of Pyrgulop- Fontelicella, Microamnicola, Nat ricola Gregg and Taylor, 1965, sis, P. nevadensis (Stearns, 1883), has not received an- Marstonia F. C. Baker, 1926, and Mexistiobia Hershler, 1985 atomical study, the penes of several eastern species have are allocated to Pyrgulopsis. been examined by Thompson (1977), who suggested that The ranges of both Tryonia and Pyrgulopsis include parts the genus may be a nymphophiline. -
DUCK HUNTING in VICTORIA 2020 Background
DUCK HUNTING IN VICTORIA 2020 Background The Wildlife (Game) Regulations 2012 provide for an annual duck season running from 3rd Saturday in March until the 2nd Monday in June in each year (80 days in 2020) and a 10 bird bag limit. Section 86 of the Wildlife Act 1975 enables the responsible Ministers to vary these arrangements. The Game Management Authority (GMA) is an independent statutory authority responsible for the regulation of game hunting in Victoria. Part of their statutory function is to make recommendations to the relevant Ministers (Agriculture and Environment) in relation to open and closed seasons, bag limits and declaring public and private land open or closed for hunting. A number of factors are reviewed each year to ensure duck hunting remains sustainable, including current and predicted environmental conditions such as habitat extent and duck population distribution, abundance and breeding. This review however, overlooks several reports and assessments which are intended for use in managing game and hunting which would offer a more complete picture of habitat, population, abundance and breeding, we will attempt to summarise some of these in this submission, these include: • 2019-20 Annual Waterfowl Quota Report to the Game Licensing Unit, New South Wales Department of Primary Industries • Assessment of Waterfowl Abundance and Wetland Condition in South- Eastern Australia, South Australian Department for Environment and Water • Victorian Summer waterbird Count, 2019, Arthur Rylah Institute for Environmental Research As a key stakeholder representing 17,8011 members, Field & Game Australia Inc. (FGA) has been invited by GMA to participate in the Stakeholder Meeting and provide information to assist GMA brief the relevant Ministers, FGA thanks GMA for this opportunity. -
Heritage of the Birdsville and Strzelecki Tracks
Department for Environment and Heritage Heritage of the Birdsville and Strzelecki Tracks Part of the Far North & Far West Region (Region 13) Historical Research Pty Ltd Adelaide in association with Austral Archaeology Pty Ltd Lyn Leader-Elliott Iris Iwanicki December 2002 Frontispiece Woolshed, Cordillo Downs Station (SHP:009) The Birdsville & Strzelecki Tracks Heritage Survey was financed by the South Australian Government (through the State Heritage Fund) and the Commonwealth of Australia (through the Australian Heritage Commission). It was carried out by heritage consultants Historical Research Pty Ltd, in association with Austral Archaeology Pty Ltd, Lyn Leader-Elliott and Iris Iwanicki between April 2001 and December 2002. The views expressed in this publication are not necessarily those of the South Australian Government or the Commonwealth of Australia and they do not accept responsibility for any advice or information in relation to this material. All recommendations are the opinions of the heritage consultants Historical Research Pty Ltd (or their subconsultants) and may not necessarily be acted upon by the State Heritage Authority or the Australian Heritage Commission. Information presented in this document may be copied for non-commercial purposes including for personal or educational uses. Reproduction for purposes other than those given above requires written permission from the South Australian Government or the Commonwealth of Australia. Requests and enquiries should be addressed to either the Manager, Heritage Branch, Department for Environment and Heritage, GPO Box 1047, Adelaide, SA, 5001, or email [email protected], or the Manager, Copyright Services, Info Access, GPO Box 1920, Canberra, ACT, 2601, or email [email protected]. -
Annual Report 2013 - 2014
Lockhart River Aboriginal Shire Council Annual Report 2013 - 2014 Page 0 Lockhart River Aboriginal Shire Council TABLE OF CONTENTS INTRODUCTION ............................................................................................................................ 2 MAP OF LOCKHART RIVER ....................................................................................................... 3 MAP OF LOCKHART RIVER TOWNSHIP .................................................................................. 4 COUNCIL VISION, MISSION STATEMENT AND GUIDING VALUES .................................... 5 MAYOR’S REPORT ...................................................................................................................... 6 CHIEF EXECUTIVE OFFICER’S REPORT ................................................................................. 7 LOCKHART RIVER HISTORY ..................................................................................................... 8 FACILITIES AND SERVICES ..................................................................................................... 12 PRIVATE ENTERPRISES ........................................................................................................... 15 OUR COUNCIL ............................................................................................................................ 17 ELECTED MEMBERS ................................................................................................................................................. 18 COUNCILLORS -
Molecular Phylogeny and Biogeography of Spring-Associated Hydrobiid Snails of the Great Artesian Basin, Australia
Molecular Phylogenetics and Evolution 34 (2005) 545–556 www.elsevier.com/locate/ympev Molecular phylogeny and biogeography of spring-associated hydrobiid snails of the Great Artesian Basin, Australia Kathryn E. Pereza,¤, Winston F. Ponderb, Donald J. Colganb, Stephanie A. Clarkc,1, Charles Lydearda a Department of Biological Sciences, Biodiversity and Systematics, University of Alabama, Box 870345, Tuscaloosa, AL 35487-0345, USA b Australian Museum, Sydney, NSW 2010, Australia c Centre for Biostructural and Biomolecular Research, University of Western Sydney, Hawkesbury Campus, Locked Bag 1797 Penrith South DC, NSW 1797, Australia Received 6 July 2004; revised 15 November 2004 Available online 6 January 2005 Abstract The Great Artesian Basin (GAB) of Australia underlies some of the driest parts of South Australia and Queensland and feeds numerous freshwater springs. Prominent and endangered components of the GAB spring community are snails of the family Hydro- biidae. This paper examines the evolutionary relationships of the entire hydrobiid fauna associated with the GAB, and includes appropriate non-GAB species to place the GAB fauna in a broader phylogenetic context. The Queensland genus Jardinella is a focus of this paper, providing a Wne scale examination of relationships between spring supergroups in the northeastern regions of the GAB. Maximum parsimony and Bayesian analyses performed on 16S, CO1, and combined sequence data from 40 hydrobiid taxa found four major clades of Australian taxa. The analysis revealed that at least three separate colonization events of the GAB spring fauna have occurred. Two of these are represented by considerable radiations, (1) Jardinella to the north and east and (2) Caldicochlea, Fonscochlea, and possibly Trochidrobia in South Australia. -
Prioritising Threatened Species and Threatening Processes Across Northern Australia: User Guide for Data
Prioritising threatened species and threatening processes across northern Australia User guide for data by Anna Pintor, Mark Kennard, Jorge G. Álvarez-Romero and Stephanie Hernandez © James Cook University, 2019 Prioritising threatened species and threatening processes across northern Australia: User guide for data is licensed by James Cook University for use under a Creative Commons Attribution 4.0 Australia licence. For licence conditions see creativecommons.org/licenses/by/4.0 This report should be cited as: Pintor A,1 Kennard M,2 Álvarez-Romero JG,1,3 and Hernandez S.1 2019. Prioritising threatened species and threatening processes across northern Australia: User guide for data. James Cook University, Townsville. 1. James Cook University 2. Griffith University 3. ARC Centre of Excellence for Coral Reef Studies Cover photographs Front cover: Butler’s Dunnart is a threatened species which is found only on the Tiwi Islands in the Northern Territory, photo Alaric Fisher. Back cover: One of the spatially explicit maps created during this project. This report is available for download from the Northern Australia Environmental Resources (NAER) Hub website at nespnorthern.edu.au The Hub is supported through funding from the Australian Government’s National Environmental Science Program (NESP). The NESP NAER Hub is hosted by Charles Darwin University. ISBN 978-1-925800-44-9 December, 2019 Printed by Uniprint Contents Acronyms....................................................................................................................................vi -
Galilee Basin Thermal Coal Prohibition Bill Submission
Galilee Basin Thermal Coal Prohibition Bill Submission This submission relates to the proposed Bill for an Act to prohibit the mining of thermal coal in the Galilee Basin. The Black-throated Finch Recovery Team is a community-based group whose mission is to secure the conservation of the Black-throated Finch (southern subspecies) Poephila cincta cincta which is listed as Endangered under the Commonwealth Environment Protection and Biodiversity Conservation Act 1999 (EPBC Act) as well as under Queensland and New South Wales state legislation. The proposed Bill is relevant to the conservation of the Black-throated Finch because of the vital importance of the Galilee Basin as a stronghold for the species. Portions of the Galilee Basin provide high quality habitat in narrow-leaf ironbark (Eucalyptus crebra) and other woodlands and these areas support the highest know densities and largest known surviving populations of the bird. The only other area known to support relatively large populations is the Townsville Coastal Plain where the species is threatened by urban expansion, intensive livestock grazing and vegetation change, including weed invasion. The species is rare, if not extinct, further south in Queensland and in New South Wales. Open-cut and underground coal mining present a major threat to the populations of Black- throated Finch in the Galilee Basin. These threats relate to mine footprints themselves, which can be substantial, especially in the case of open-cut mining, and to the direct and indirect effects of mining-related infrastructure. Offsets, as proposed for as part of the conditions for approval of developments, such as the Carmichael Mine, do not compensate for loss of habitat and populations of Black-throated Finch and there is the very real risk that there are inadequate areas suitable for offsets. -
Why Do Coal Mines Need So Much Water? 13 April 2017, by Ellen Moon
Why do coal mines need so much water? 13 April 2017, by Ellen Moon as a water-based slurry for further processing. Mines also need water for things like equipment maintenance, and for consumption by the mining communities themselves. In total, about 250 litres of freshwater are required per tonne of coal produced. This freshwater makes up around a quarter of the total water demand during coal production, the rest being "worked" (recycled) water. Coal mines, such as this one near Bowen, use water for What other industries use lots of water? everything from equipment cooling to dust management. Credit: CSIRO, CC BY The Great Artesian Basin is one of the largest underground water reservoirs in the world. It underlies 22% of Australia's land area, beneath the arid and semi-arid parts of Queensland, New South From accidental water spills into coastal wetlands, Wales, South Australia and the Northern Territory. to proposed taxpayer-funded loans, Adani's planned Carmichael coal mine and the associated Its aquifers supply water to around 200 towns or Abbot Point coal terminal can't keep out of the settlements, most of which are allowed to draw news at the moment. between 100 and 500 million litres (ML) per year. Last week, the granting of an unlimited 60-year water licence to the Carmichael mine, in Queensland's Galilee Basin, rattled environmentalists, farmers and community groups alike. In a region experiencing prolonged drought conditions, the provision of unlimited water for one of the largest mining operations in the Southern Hemisphere seems like a commitment at odds with current climate predictions. -
Guided by Her: Aboriginal Women's Participation in Australian Expeditions
5 Guided by her: Aboriginal women’s participation in Australian expeditions Allison Cadzow I was compelled in a great measure to be guided by her. She was acquainted with all their haunts and was a native of Port Davey, belonging to this tribe and having a brother and other relatives living among them, [Low. Ger Nown] was her native place. Though I knew she intended sojourning with them, yet there was no alternative but to follow her suggestions … George Augustus Robinson discussing Dray’s guiding in Tasmania (6 April 1830) Our female guide, who had scarcely before ventured to look up, stood now boldly forward, and addressed the strange tribe in a very animated and apparently eloquent manner; and when her countenance was thus lighted up, displaying fine teeth, and great earnestness of manner, I was delighted to perceive what soul the woman possessed, and could not but consider our party fortunate in having met with such an interpreter. Thomas Mitchell discussing Turandurey’s guiding in New South Wales (12 May 1836) The Aboriginal women mentioned above are clearly represented as guides and appear in plain view; they are not in hiding. While women did hide from white expedition members – for good reason considering 85 BRoKERS AND BouNDARIES the frequent violence of white people towards them – this was not the only reaction they had. Historians have largely ignored Aboriginal women’s involvement in exploration expeditions, though there are some notable exceptions in the work of Henry Reynolds, Lyndall Ryan and Donald Baker. Some other authors who have attended to them, such as Philip Clarke, imply that women were invariably hidden away during encounters, suggesting they were not actively involved in expeditions.1 Even when women did hide, this was not necessarily the end of the story, as they sometimes re-emerged after assessing the situation. -
Bayardella Burch, 1977
Bayardella Burch, 1977 Diagnostic features Snails with small neritiform or cylindrical shell with a low spire. The shell surface has raised spiral ribs and transverse striae, giving appearance of small, incised rectangles The aperture length is almost equal to the whole shell, and has a continuous periostracal fringe. The columellar margin is reflected and slightly curved, without a columellar fold. A deep umbilicus is present. The copulatory organ has an accessory bursa, but lacks a flagellum. A large muscular bulb is suspended from the proximal end of the praeputium, into which the duct of the accessory bursa opens. The anus lies on the anterior edge of rectal lobe. Classification Class Gastropoda Infraclass Heterobranchia Megaorder Hygrophila Order Lymnaeida Superfamily Planorboidea Family Planorbidae Subfamily: Miratestinae Genus Bayardella Burch, 1977 Type species: Plesiophysa (Bayardella) johni Burch, 1977 Original reference: Burch, J.B. (1977). A new freshwater snail (Basommatophora : Planorbidae) from Australia, Plesiophysa (Bayardella) johni. Malacological Review 10: 79-80. Type locality: sdell River, Walcott nlet, north Western Australia. State of taxonomy We follow Walker (1988). We know of at least one undescribed species of Bayardella. Biology and ecology Under wood and stones, in streams and waterholes. At least one species (B. cosmeta) capable of aestivation (Smith and Burn, 1976); biology otherwise unstudied. Distribution Northern, central and eastern Australian mainland. Notes Only Glyptophysa (Glyptophysa) aliciae has similar heavy periostracal spiral ridges. Bayardella has a narrower and much smaller spire and a less distinct shoulder and is smaller in size than G. (G) aliciae. Bayardella also has a much larger aperture compared to G. (G) aliciae.