Wildlife Order 2010
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Wildlife Act 1953
Reprint as at 7 August 2020 Wildlife Act 1953 Public Act 1953 No 31 Date of assent 31 October 1953 Commencement see section 1(2) Contents Page Title 7 1 Short Title and commencement 7 2 Interpretation 7 2A Meaning of possession 14 2B Application of certain provisions restricted 15 Part 1 Protection of wildlife 3 Wildlife to be protected 15 4 Certain wildlife declared to be game 16 5 Certain wildlife partially protected 16 6 Certain wildlife may be hunted subject to conditions imposed by 16 the Minister 7 Certain wildlife not protected 17 7A Wild animals 17 7B Terrestrial and freshwater invertebrates 18 7BA Marine species 18 7C Farming certain unprotected animals 18 8 Alteration of schedules 19 Note Changes authorised by subpart 2 of Part 2 of the Legislation Act 2012 have been made in this official reprint. Note 4 at the end of this reprint provides a list of the amendments incorporated. This Act is administered by the Department of Conservation. 1 Reprinted as at Wildlife Act 1953 7 August 2020 Wildlife sanctuaries 9 Wildlife sanctuaries 19 10 All wildlife in sanctuaries absolutely protected 23 11 Destruction or seizure of certain animals found in sanctuaries 24 12 Mining privileges, coal mining rights, and public works 24 [Repealed] 13 Seizure of wildlife, etc, illegally taken 24 Wildlife refuges 14 Wildlife refuges 25 Wildlife management reserves 14A Wildlife management reserves 28 14AA Granting of concessions in wildlife sanctuaries, wildlife refuges, 30 and wildlife management reserves Management planning 14B Wildlife areas to be -
CATALINA CALIFORNIA QUAIL (Callipepla Californica Catalinensis) Paul W
II SPECIES ACCOUNTS Andy Birch PDF of Catalina California Quail account from: Shuford, W. D., and Gardali, T., editors. 2008. California Bird Species of Special Concern: A ranked assessment of species, subspecies, and distinct populations of birds of immediate conservation concern in California. Studies of Western Birds 1. Western Field Ornithologists, Camarillo, California, and California Department of Fish and Game, Sacramento. California Bird Species of Special Concern CATALINA CALIFORNIA QUAIL (Callipepla californica catalinensis) Paul W. Collins Criteria Scores Population Trend 0 Santa Range Trend 0 Barbara County Population Size 7.5 Range Size 10 Ventura Endemism 10 County Population Concentration 10 Threats 0 Los San Miguel Is. Santa Cruz Is. Angeles County Anacapa Is. Santa Rosa Is. Santa Barbara Is. Santa Catalina Is. San Nicolas Is. San Clemente Is. Current Year-round Range Historic Year-round Range County Boundaries Kilometers 20 10 0 20 Current and historic (ca. 1944) year-round range of the Catalina California Quail. Birds from Santa Catalina Island (perhaps brought by Native Americans) later introduced successfully to Santa Rosa (1935–1940) and Santa Cruz (late 1940s) islands, but unsuccessfully to San Nicolas Island (1962); quail from mainland populations of C. c. californica introduced unsuccessfully to Santa Cruz (prior to 1875) and San Clemente (late 19th century, 1913) islands. Catalina California Quail Studies of Western Birds 1:107–111, 2008 107 Studies of Western Birds No. 1 SPECIAL CONCERN PRIORITY HISTORIC RANGE AND ABUNDANCE Currently considered a Bird Species of Special IN CALIFORNIA Concern (year round), priority 3. This subspecies Grinnell and Miller (1944) described the Catalina was not included on prior special concern lists California Quail as a “common to abundant” (Remsen 1978, CDFG 1992). -
Eastern Rosella (Platycercus Eximius)
Eastern rosella (Platycercus eximius) Class: Aves Order: Psittaciformes Family: Psittaculidae Characteristics: The Eastern rosella averages 30 cm (12 in) in length and 99gm (3.5oz) in weight. With a red head and white cheeks, the upper breast is red and the lower breast is yellow fading to pale green over the abdomen. The feathers of the back and shoulders are black, and have yellowish or greenish margins giving rise to a scalloped appearance that varies slightly between three subspecies and the sexes. The wings and lateral tail feathers are bluish while the tail is dark green. Range & Habitat: Behavior: Like most parrots, Eastern rosellas are cavity nesters, generally Eastern Australia down to nesting high in older large trees in forested areas. They enjoy bathing in Tasmania in wooded country, puddles of water in the wild and in captivity and frequently scratch their open forests, woodlands and heads with the foot behind the wing. Typical behavior also includes an parks. Nests in tree cavities, undulating flight, strutting by the male, and tail wagging during various stumps or posts. displays such as courting, and a high-pitched whistle consisting of sharp notes repeated rapidly in quick succession. Reproduction: Breeding season is influenced by rain and location. Courting male bows while sounding out mating call followed by mutual feeding and then mating. Female alone incubates eggs while male bring food. 2-9 eggs will hatch in 18 - 20 days. Hatchlings are ready to leave the nest in about 5 weeks but may stay with their parents for several months unless there is another mating. -
A Possible Brown Skua (<I>Stercorarius Antarcticus</I>) On
lan McLaren mer (June-August)specimens in Canadi- in both publishedarticles and material an museumscollected prior to 1980 in At- postedon the WorldWideWeb,has indicat- BiologyDepartment lantic Canada have been critically identi- edto us thatthe Sable Island bird strongly fied as South Polar Skuas (Michel resembledBrown Skua, although deficien- DalhousieUniversity Gossefin, National Museum of Canada, cies in this information lead us to leave it pers. comm.;University of WesternOn- formallyunidentified. Halifax,Nova Scotia B3H 4J1 tario [seebelow]). All GreatSkua speci- mens have come from the Grand Banks: an ([email protected]) BACKGROUND ON CONFIRMED AND immature in late August 1961 (D. POSSIBLE BROWN SKUAS IN THE McAlpine,New Brunswick Museum, pers. NORTH ATLANTIC Zoe Lucas comm.)and severaladults in September Even after Chilean (S. chilensis)and South (M. Gossefin,pers. comm.). The Great Polar Skuaswere recognizedas distinct P.O.Box 64, Halifax CRO Skuaslisted for SableIsland by McLaren species,the three other skua taxa in the (1980)were not criticallyidentified. Nova Southern Hemisphere continued to be Halifax,Nova Scotia B3J 2L4 Scotianobservers have attemptedto dis- classifiedas formsof GreatSkua (e.g., tinguishthe two speciessince at leastthe Devillers1977). BrownSkna, however, has early 1980s.Since 1992, Lucas has studied becomegenerally recognized as a distinct six live Great Skuas on Sable Island at fair- specieswith threesubspecies (e.g., Olsen ABSTRRCT ly closerange and has found five tideline and Larsson 1997): Falkland Skua, -
TAG Operational Structure
PARROT TAXON ADVISORY GROUP (TAG) Regional Collection Plan 5th Edition 2020-2025 Sustainability of Parrot Populations in AZA Facilities ...................................................................... 1 Mission/Objectives/Strategies......................................................................................................... 2 TAG Operational Structure .............................................................................................................. 3 Steering Committee .................................................................................................................... 3 TAG Advisors ............................................................................................................................... 4 SSP Coordinators ......................................................................................................................... 5 Hot Topics: TAG Recommendations ................................................................................................ 8 Parrots as Ambassador Animals .................................................................................................. 9 Interactive Aviaries Housing Psittaciformes .............................................................................. 10 Private Aviculture ...................................................................................................................... 13 Communication ........................................................................................................................ -
Captive Wild Animal Farm License Application
Mail to: Department of Natural Resources Captive Wild Animal Farm Captive Wildlife - CS/1 License Application PO Box 7924 Madison, WI 53707-7924 dnr.wi.gov Consult the attached instructions before completing Notice: Pursuant to ch. 169, Wis. Stats., and ch. NR 16, Wis. Adm. Code, Fees: completion of this form is required to apply for a captive wild animal farm license. Class A Captive Wild Animal Farm Operation of a captive wild animal farm without a license may result in forfeitures (Annual sales of $10,000 or more) of up to $500 in addition to suspension of eligibility for future licenses. A social $200 Initial license $100 Annual renewal security number or federal employer identification number is REQUIRED when applying for licenses according to ss. 169.34 and 169.35, Wis. Stats., but it may Class B Captive Wild Animal Farm not be disclosed by the Department of Natural Resources (DNR) to anyone (Annual sales less than $10,000) except the Departments of Children and Families, Workforce Development or the $50 Initial license $ 25 Annual renewal Department of Revenue. Personal information collected may be used for participation in surveys, eligibility for approvals, law enforcement and other $ 0 Sport Club or 4-H member under age 14. secondary purposes and may be provided to requesters to the extent required by Attach proof of current membership Wisconsin's Open Records laws (ss. 19.31-19.39, Wis. Stats.). + $20 Late fee if application filed after license expiration date. A. Applicant Information Last Name First MI DNR Customer ID Current License # (if renewal) Address Date of Birth (mm/dd/yyyy) SSN OR FEIN City State ZIP Code Daytime Phone (incl. -
Body Temperatures in California and Gambel's Quail
150 Baa•oz,o•awand DawsoN, California and Gambel's Quail [1VoL Auk 75 BODY TEMPERATURES IN CALIFORNIA AND GAMBEL'S QUAIL BY GEORGE A. BARTHOLOMEW AND WILLIAM R. DAWSON Tm• paucity of data on the body temperaturesof small gallinaceous birds prompts us to report miscellaneousobservations which we have made over the past severalyears on the body temperaturesof the Cali- fornia Quail, Lophortyxcalifornicus, a commonresident in grasslandand chaparral from southernOregon to southern Baja Cal/fornia, and the Gambel's Quail, L. œambelii,a residentin the desert regionsof south- western United States and northwestern Mexico. The habitats of both speciesare characterizedby high summer temperaturesand moderate winter conditions. We have therefore paid particular attention to capacity for temperature regulation in hot environments. We found that when ambient (environmental)temperature rose, the birds' body temperaturecould rise by as much as 4ø C. (7.2ø F.), without ill effects. Ability to maintain above normal body temperatures higher than ambient temperaturesfacilitates transfer of excessbody heat to the environment. It is probablya major avian adaptationto hot conditions. The data presentedwere acquiredincidental to work on other species and for that reasonare not comprehensive,but they serveto characterize aspectsof temperatureregulation in quail. MATERIALS AND METHODS The observationswere made on 8 adult and 2 juvenile California Quailcaptured on the LosAngeles campus of the Universityof California, and on 5 adult and 2 juvenile Gambers Quail capturedin the Colorado Desert, three miles south of Calipatria, Imperial County, California. The captive animals of both specieswere housedin cagesof half-inch wire mesh wh/ch measured 12 x 12 x 24 inches and had sand-covered floors. -
BROWN SKUAS Stercorarius Antarcticus INCUBATE a MACARONI PENGUIN EUDYPTES CHRYSOLOPHUS EGG at MARION ISLAND
Clokie & Cooper: Skuas incubate a Macaroni Penquin egg 59 BROWN SKUAS STERCORARIUS antarcticus INCUBATE A MACARONI PENGUIN EUDYPTES CHRYSOLOPHUS EGG AT MARION ISLAND LINDA CLOKIE1 & JOHN COOPER2,3 1Marine & Coastal Management Branch, Department of Environmental Affairs, Private Bag X2, Rogge Bay 8012, South Africa 2Animal Demography Unit, Department of Zoology, University of Cape Town, Rondebosch 7701, South Africa 3DST/NRF Centre of Excellence for Invasion Biology, Department of Botany and Zoology, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa ([email protected]) Received 3 October 2009, accepted 5 February 2010 Brown/Sub-antarctic Skua Stercorarius antarcticus are widely -sized for skua eggs, thus deemed to be the birds’ own clutch, but distributed at cool-temperate and sub-Antarctic islands in the the third was an all-white egg (Fig. 1). This egg was noticeably Southern Ocean, where their diet includes burrowing petrels caught larger than the two skua eggs, and was more rounded in shape. at night and eggs stolen from incubating birds, especially penguins, On 19 December when the nest was revisited one of the two skua during the day (Furness 1987, Higgins & Davies 1996, Shirihai eggs was no longer present. During visits on 21 December 2008 2007). At Marion Island, Prince Edward Islands in the southern and on 4 and 15 January 2009 only the white egg was present, and Indian Ocean, Brown Skua prey on eggs of crested penguins the displaced incubating bird was quick to defend its nest. On 9 Eudyptes sp. during summer months which they remove in their February 2009 the skua pair was still present at the nest, with one bills from the colonies by flying to nearby middens where the eggs’ bird in an incubating position, but the nest was empty of contents. -
Free Download! the Trumpeter Swan
G3647 The Trumpeter Swan by Sumner Matteson, Scott Craven and Donna Compton Snow-white Trumpeter Swans present a truly spectac- Swans of the Midwest ular sight. With a wingspan of more than 7 feet and a rumpeter Swans, along with ducks and geese, belong height of about 4 feet, the Trumpeter Swan (Cygnus buc- to the avian Order Anseriformes, Family Anatidae. cinator) ranks as the largest native waterfowl species in T Trumpeters have broad, flat bills with fine tooth-like North America. serrations along the edges which allow them to strain Because the Trumpeter Swan disappeared as a breed- aquatic plants and water. The birds’ long necks and ing bird in the Midwest, several states have launched strong feet allow them to uproot plants in water up to 4 restoration programs to reintroduce it to the region. This feet deep. publication will provide you with background informa- Most Trumpeter Swans weigh 21–30 pounds, tion on the Trumpeter Swan’s status and life history, and although some males exceed the average weight. The on restoration efforts being conducted in the upper male is called a cob; the female is called a pen; and a swan Midwest. in its first year is called a cygnet or juve- nile. The Trumpeter is often con- fused with the far more common Tundra Swan (formerly Whistling Swan, Cygnus columbianus), the only other native swan found routinely in North America. Tundra Swans can be seen in the upper Trumpeter Swan Midwest only during spring and fall migration. You can distinguish between the two native species most accurately by listening to their calls. -
Austromonticola, a New Genus of Broad-Nosed Weevil (Coleoptera, Curculionidae, Entiminae) from Montane Areas of New Zealand
A peer-reviewed open-access journal ZooKeys 707: 73–130 (2017) Revision of Austromonticola weevils 73 doi: 10.3897/zookeys.707.12649 MONOGRAPH http://zookeys.pensoft.net Launched to accelerate biodiversity research Austromonticola, a new genus of broad-nosed weevil (Coleoptera, Curculionidae, Entiminae) from montane areas of New Zealand Samuel D. J. Brown1,2 1 Bio-Protection Research Centre, PO Box 85084, Lincoln University 7647, Canterbury, New Zealand 2 AgResearch, Gerald St, Lincoln, Canterbury, New Zealand Corresponding author: Samuel D. J. Brown ([email protected]) Academic editor: M. Alonso-Zarazaga | Received 17 March 2017 | Accepted 20 August 2017 | Published 10 October 2017 http://zoobank.org/0DF0C91D-3B1D-450D-80F3-F32F8EE7801D Citation: Brown SDJ (2017) Austromonticola, a new genus of broad-nosed weevil (Coleoptera, Curculionidae, Entiminae) from montane areas of New Zealand. ZooKeys 707: 73–130. https://doi.org/10.3897/zookeys.707.12649 Abstract Austromonticola gen. n. is proposed for a group of eight New Zealand alpine broad-nosed weevil species, all of which are here described: A. atriarius sp. n. (type locality: Umbrella Mountains, Central Otago), A. caelibatus sp. n. (type locality: Ohau Range, Mackenzie), A. furcatus sp. n. (type locality: Old Man Range, Central Otago), A. inflatus sp. n. (type locality: Hawkdun Range, Central Otago), A. planulatus sp. n. (type locality: St Marys Range, Central Otago), A. postinventus sp. n. (type locality: Kirkliston Range, South Canterbury), A. mataura sp. n. (type locality: Mt Dick, Otago Lakes) and A. rotundus sp. n. (type locality: Old Man Range, Central Otago). All species occur exclusively above 1000 m elevation in the mountains of Central Otago and South Canterbury in the South Island. -
Project River Recovery Bibliography
Project River Recovery bibliography 1991–July 2007 CANTERBURY SERIES 0208 Project River Recovery bibliography 1991 – JULY 2007 Project River Recovery Report 2007/02 Susan Anderson Department of Conservation, Private Bag, Twizel July 2007 Docdm-171819 - PRR Bibliography 2 INTRODUCTION Since its inception in 1991, Project River Recovery has undertaken or funded numerous research projects. The results of these investigations have been reported in various reports, theses, Department of Conservation publications, and scientific papers. Results of all significant research have been published, can be found through literature searches, and are widely available. Internal reports that do not warrant publication are held at the Twizel Te Manahuna Area Office and at the main Department of Conservation library in Wellington. All unpublished Project River Recovery reports produced since 1998 have been assigned report numbers. In addition to reports on original research, Project River Recovery has produced magazine articles and newspaper feature articles, various annual reports, progress reports, discussion documents, and plans. It has also commissioned some reports from consultants. This bibliography updates the bibliography compiled in 2000 (Sanders 2000) and lists all reports, theses, diplomas, Department of Conservation publications, and scientific papers that were produced or supported by Project River Recovery between 1991 and July 2007. It does not list brochures, posters, fact sheets, newsletters, abstracts for conference programmes, or minor magazine or newspaper articles. Docdm-171819 - PRR Bibliography 3 BIBLIOGRAPHY Adams, L.K. 1995: Reintroduction of juvenile black stilts to the wild. Unpublished MSc thesis, University of Canterbury, Christchurch. 108 p. Anderson, S.J. 2006: Proposal for black-fronted tern nest monitoring and predator trapping at the Ruataniwha Wetlands: 2006-2007 breeding season. -
Partridges, Quails, Pheasants and Turkeys Phasianidae Vigors, 1825: Zoological Journal 2: 402 – Type Genus Phasianus Linnaeus, 1758
D .W . .5 / DY a 5D t w[ { wt Ç"" " !W5 í ÇI &'(' / b ù b a L w 5 ! ) " í "* " Ç t+ t " h " * { b ù" t* &)/&0 Order GALLIFORMES: Game Birds and Allies The order of galliform taxa in Checklist Committee (1990) appears to have been based on Peters (1934). Johnsgard (1986) synthesised available data, came up with similar groupings of taxa, and produced a dendrogram indicating that turkeys (Meleagridinae) were the most primitive (outside Cracidae and Megapodiidae), with grouse (Tetraoninae), guineafowl (Numidinae), New World quails (Odontophorinae) and pheasants and kin (Phasianinae) successively more derived. Genetic evidence (DNA-hybridisation data) provided by Sibley & Ahlquist (1990) suggested Odontophorinae were the most basal phasianoids and guineafowl the next most basal group. A basal position of the New World quails among phasianoids has been supported by other genetic data (Kimball et al. 1999, Armstrong et al. 2001). A recent analysis based on morphological characters (Dyke et al. 2003) found support for megapodes as the most basal group in the order, then Cracidae, then Phasianidoidea, and within the latter, Numididae the most basal group. In contrast to the above genetic-based analyses, Dyke et al. (2003) found the Odontophorinae to be the most derived group within the order. A recent analysis using both mitochondrial ND2 and cytochrome-b DNA sequences, however, reinforces the basal position of the Odontophorinae (Pereira & Baker 2006). Here we follow a consensus of the above works and place Odontophorinae basal in the phasianids. Worthy & Holdaway (2002) considered that Cheeseman’s (1891) second-hand record of megapodes from Raoul Island, Kermadec Group, before the 1870 volcanic eruption has veracity.