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Mount Canobolas Fauna Survey
MOUNT CANOBOLAS FAUNA SURVEY 24TH – 29th MARCH 2019 1 Introduction Mount Canobolas State Conservation Area The Mount Canobolas State Conservation Area (SCA) Draft Plan of Management begins with the following vision for this reserve: Mount Canobolas State Conservation Area is a sentinel in the landscape. It is a park valued, understood and protected by the community for its uniqueness, biodiversity, visitor experiences, and for the spiritual and cultural connections between people and this special place, now and into the future (OEH 2018). This iconic place is an extinct volcano rising to an altitude of 1397m asl and more than 500m above the surrounding central tablelands landscape. It has great significance for the local Wiradjuri custodians. The ecological values of this place are shaped by its high altitude, volcanic origins, isolation from similar geological formations and the extensive clearing of the surrounding landscape leaving it as a relatively isolated remnant of native vegetation. The presence of sub-alpine communities is particularly noteworthy (OEH 2018). The SCA incorporates an area of 1672 ha. The vegetation communities of the Mt Canobolas SCA have been broadly described and mapped with the following communities defined: 1. Eucalyptus macrorhyncha – E. dives: shrubby open forest and woodland (26% of the SCA) a. E. macrorhyncha dominant in more exposed sites b. E. dives dominant in less exposed sites 2. E. pauciflora – E. dalrympleana: Grassy woodlands and tall open forests (51% of the SCA) a. E. pauciflora – E. canobolensis grassy woodlands b. E. dalrympleana – E. viminalis tall open forests 3. Outcrop low open woodland (E. canobolensis – E. petroc?) and / or shrubs 4. -
Web-Book Catalog 2021-05-10
Lehigh Gap Nature Center Library Book Catalog Title Year Author(s) Publisher Keywords Keywords Catalog No. National Geographic, Washington, 100 best pictures. 2001 National Geogrpahic. Photographs. 779 DC Miller, Jeffrey C., and Daniel H. 100 butterflies and moths : portraits from Belknap Press of Harvard University Butterflies - Costa 2007 Janzen, and Winifred Moths - Costa Rica 595.789097286 th tropical forests of Costa Rica Press, Cambridge, MA rica Hallwachs. Miller, Jeffery C., and Daniel H. 100 caterpillars : portraits from the Belknap Press of Harvard University Caterpillars - Costa 2006 Janzen, and Winifred 595.781 tropical forests of Costa Rica Press, Cambridge, MA Rica Hallwachs 100 plants to feed the bees : provide a 2016 Lee-Mader, Eric, et al. Storey Publishing, North Adams, MA Bees. Pollination 635.9676 healthy habitat to help pollinators thrive Klots, Alexander B., and Elsie 1001 answers to questions about insects 1961 Grosset & Dunlap, New York, NY Insects 595.7 B. Klots Cruickshank, Allan D., and Dodd, Mead, and Company, New 1001 questions answered about birds 1958 Birds 598 Helen Cruickshank York, NY Currie, Philip J. and Eva B. 101 Questions About Dinosaurs 1996 Dover Publications, Inc., Mineola, NY Reptiles Dinosaurs 567.91 Koppelhus Dover Publications, Inc., Mineola, N. 101 Questions About the Seashore 1997 Barlowe, Sy Seashore 577.51 Y. Gardening to attract 101 ways to help birds 2006 Erickson, Laura. Stackpole Books, Mechanicsburg, PA Birds - Conservation. 639.978 birds. Sharpe, Grant, and Wenonah University of Wisconsin Press, 101 wildflowers of Arcadia National Park 1963 581.769909741 Sharpe Madison, WI 1300 real and fanciful animals : from Animals, Mythical in 1998 Merian, Matthaus Dover Publications, Mineola, NY Animals in art 769.432 seventeenth-century engravings. -
A Guide to the Birds of Barrow Island
A Guide to the Birds of Barrow Island Operated by Chevron Australia This document has been printed by a Sustainable Green Printer on stock that is certified carbon in joint venture with neutral and is Forestry Stewardship Council (FSC) mix certified, ensuring fibres are sourced from certified and well managed forests. The stock 55% recycled (30% pre consumer, 25% post- Cert no. L2/0011.2010 consumer) and has an ISO 14001 Environmental Certification. ISBN 978-0-9871120-1-9 Gorgon Project Osaka Gas | Tokyo Gas | Chubu Electric Power Chevron’s Policy on Working in Sensitive Areas Protecting the safety and health of people and the environment is a Chevron core value. About the Authors Therefore, we: • Strive to design our facilities and conduct our operations to avoid adverse impacts to human health and to operate in an environmentally sound, reliable and Dr Dorian Moro efficient manner. • Conduct our operations responsibly in all areas, including environments with sensitive Dorian Moro works for Chevron Australia as the Terrestrial Ecologist biological characteristics. in the Australasia Strategic Business Unit. His Bachelor of Science Chevron strives to avoid or reduce significant risks and impacts our projects and (Hons) studies at La Trobe University (Victoria), focused on small operations may pose to sensitive species, habitats and ecosystems. This means that we: mammal communities in coastal areas of Victoria. His PhD (University • Integrate biodiversity into our business decision-making and management through our of Western Australia) -
The Role of Habitat Variability and Interactions Around Nesting Cavities in Shaping Urban Bird Communities
The role of habitat variability and interactions around nesting cavities in shaping urban bird communities Andrew Munro Rogers BSc, MSc Photo: A. Rogers A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2018 School of Biological Sciences Andrew Rogers PhD Thesis Thesis Abstract Inter-specific interactions around resources, such as nesting sites, are an important factor by which invasive species impact native communities. As resource availability varies across different environments, competition for resources and invasive species impacts around those resources change. In urban environments, changes in habitat structure and the addition of introduced species has led to significant changes in species composition and abundance, but the extent to which such changes have altered competition over resources is not well understood. Australia’s cities are relatively recent, many of them located in coastal and biodiversity-rich areas, where conservation efforts have the opportunity to benefit many species. Australia hosts a very large diversity of cavity-nesting species, across multiple families of birds and mammals. Of particular interest are cavity-breeding species that have been significantly impacted by the loss of available nesting resources in large, old, hollow- bearing trees. Cavity-breeding species have also been impacted by the addition of cavity- breeding invasive species, increasing the competition for the remaining nesting sites. The results of this additional competition have not been quantified in most cavity breeding communities in Australia. Our understanding of the importance of inter-specific interactions in shaping the outcomes of urbanization and invasion remains very limited across Australian communities. This has led to significant gaps in the understanding of the drivers of inter- specific interactions and how such interactions shape resource use in highly modified environments. -
Contributions to the Reproductive Effort in a Group of Plural-Breeding Pied Butcherbirds Cracticus Nigrogularis
Australian Field Ornithology 2012, 29, 169–181 Contributions to the reproductive effort in a group of plural-breeding Pied Butcherbirds Cracticus nigrogularis D.G. Gosper 39 Azure Avenue, Balnarring VIC 3926, Australia Email: [email protected] Summary. Concurrent nesting by two females from a single social group of Pied Butcherbirds Cracticus nigrogularis is described. Young fledged from two nests in the first 2 years, but breeding failed in the following two seasons after Australian Magpies C. tibicen displaced the group from its original nest-tree. The two breeding females in the Pied Butcherbird group constructed their nests and incubated synchronously in the same tree without conflict. Only the females constructed the nest and incubated the eggs. Other group members fed the females before laying and during incubation. Females begged for food using a display resembling that of juvenile Butcherbirds. Most (and probably all) members of the group fed the nestlings and fledglings, with multiple members delivering food to the young in both nests and removing or eating faecal sacs. Immatures at the beginning of their second year, with no previous experience, performed the full range of helping tasks, including the provisioning of females from the pre-laying stage. During the nestling stage, the group fed on nectar from Silky Oaks Grevillea robusta, but did not feed this to the young. Introduction The Pied Butcherbird Cracticus nigrogularis (Artamidae) may breed co-operatively (Rowley 1976; Dow 1980; Clarke 1995). Higgins et al. (2006) considered it to be an occasional co-operative breeder, although the only detailed study to date (i.e. -
The Marine Biodiversity and Fisheries Catches of the Pitcairn Island Group
The Marine Biodiversity and Fisheries Catches of the Pitcairn Island Group THE MARINE BIODIVERSITY AND FISHERIES CATCHES OF THE PITCAIRN ISLAND GROUP M.L.D. Palomares, D. Chaitanya, S. Harper, D. Zeller and D. Pauly A report prepared for the Global Ocean Legacy project of the Pew Environment Group by the Sea Around Us Project Fisheries Centre The University of British Columbia 2202 Main Mall Vancouver, BC, Canada, V6T 1Z4 TABLE OF CONTENTS FOREWORD ................................................................................................................................................. 2 Daniel Pauly RECONSTRUCTION OF TOTAL MARINE FISHERIES CATCHES FOR THE PITCAIRN ISLANDS (1950-2009) ...................................................................................... 3 Devraj Chaitanya, Sarah Harper and Dirk Zeller DOCUMENTING THE MARINE BIODIVERSITY OF THE PITCAIRN ISLANDS THROUGH FISHBASE AND SEALIFEBASE ..................................................................................... 10 Maria Lourdes D. Palomares, Patricia M. Sorongon, Marianne Pan, Jennifer C. Espedido, Lealde U. Pacres, Arlene Chon and Ace Amarga APPENDICES ............................................................................................................................................... 23 APPENDIX 1: FAO AND RECONSTRUCTED CATCH DATA ......................................................................................... 23 APPENDIX 2: TOTAL RECONSTRUCTED CATCH BY MAJOR TAXA ............................................................................ -
Birds of Waite Conservation Reserve
BIRDS OF WAITE CONSERVATION RESERVE Taxonomic order & nomenclature follow Menkhorst P, Rogers D, Clarke R, Davies J, Marsack P, & Franklin K. 2017. The Australian Bird Guide. CSIRO Publishing. Anatidae Australian Wood Duck Chenonetta jubata R Pacific Black Duck Anas superciliosa R Phasianidae Stubble Quail Coturnix pectoralis R Brown Quail Coturnix ypsilophora V Ardeidae White-faced Heron Egretta novaehollandiae V Pelecanidae Australian Pelican Pelecanus conspicillatus V Accipitridae Black-shouldered Kite Elanus axillaris R Square-tailed Kite Lophoictinia isura R Little Eagle Hieraaetus morphnoides V Wedge-tailed Eagle Aquila audax R Brown Goshawk Accipiter fasciatus U Collared Sparrowhawk Accipiter cirrocephalus R Spotted Harrier Circus assimilis V Whistling Kite Haliastur sphenurus V Turnicidae Little Button-quail Turnix velox V Columbidae Feral Pigeon (Rock Dove) *Columba livia C Spotted Dove *Spilopelia chinensis R Common Bronzewing Phaps chalcoptera U Crested Pigeon +Ocyphaps lophotes C Cuculidae Horsfield’s Bronze Cuckoo Chalcites basalis R Fan-tailed Cuckoo Cacomantis flabelliformis R Tytonidae Eastern Barn Owl Tyto delicatula V Strigidae Southern Boobook Ninox boobook C Podargidae Tawny Frogmouth Podargus strigoides C Alcedinidae Laughing Kookaburra Dacelo novaeguineae C Falconidae Nankeen Kestrel Falco cenchroides R Australian Hobby Falco longipennis R Brown Falcon Falco berigora V Peregrine Falcon Falco peregrinus U Cacatuidae Yellow-tailed Black-Cockatoo Calyptorhynchus funereus C Galah Eolophus roseicapilla C Long-billed Corella -
Pied Currawong (Western Victoria)
RECOVERY OUTLINE Pied Currawong (western Victoria) 1 Family Artamidae 2 Scientific name Strepera graculina ashbyi Mathews, 1913 3 Common name Pied Currawong (western Victoria) 4 Conservation status Critically Endangered: C2b 5 Reasons for listing Grampians, Vic. (Schodde and Mason, 1999). Pure This newly-described subspecies has possibly already S. g. ashbyi, if they exist, are likely to be in south-west been hybridised out of existence. However, until Victoria but there have been no searches. confirmation of this, there is presumed to be a single, very small, decreasing population of pure-bred birds (Critically Endangered: C2b). Almost no information on the taxon exists, so it is listed on a precautionary basis. Estimate Reliability Extent of occurrence 2,000 km2 low trend decreasing low Area of occupancy 1,000 km2 low trend decreasing low No. of breeding birds 250 low trend decreasing low No. of sub-populations 1 medium 9 Ecology Pied Currawongs generally live in forest and Generation time 5 years low woodland, where they take insects and small birds and 6 Infraspecific taxa animals (Blakers et al., 1984). They also frequent S. g. crissalis (Lord Howe Island) is Endangered. settlements and orchards. They lay 2-4 eggs in their S. g. magnirostris (Cape York Peninsula), S. g. robinsoni nest made in tall trees (Beruldsen, 1980; Emison et al., (wet tropics), S. g. graculina (eastern Australia), and 1987). Nothing is known about the ecology of S. g. nebulosa (south-eastern Australia) are Least S. g. ashbyi in particular. Concern, as is the species. S. g. ashbyi may be a morph of S. -
AOU Classification Committee – North and Middle America
AOU Classification Committee – North and Middle America Proposal Set 2015-A 21 Jan 2015 No. Page Title 01 02 Revise the classification of the Pipridae 02 08 Add Bicolored Wren Campylorhynchus griseus to the Main List 03 11 Move Dusky Pigeon Patagioenas goodsoni from the Appendix to the Main List 04 14 Revise the classification of the Psittaciformes 05 19 Split Pterodroma heraldica and P. atrata from Herald Petrel P. arminjoniana 06 26 Transfer American Tree Sparrow Spizella arborea to Spizelloides 07 28 Split Passerina pallidior from Painted Bunting P. ciris 08 32 Split Toxostoma arenicola from LeConte’s Thrasher T. lecontei 09 35 Correct the scientific names of (a) Leptotila cassini and (b) Amazilia saucerrottei 10 37 Split Laysan Honeycreeper from Apapane Himatione sanguinea and change its specific epithet to fraithii 11 40 Split Newell’s Shearwater Puffinus newelli from Townsend’s Shearwater P. auricularis, and consider Rapa Shearwater P. myrtae as a species separate from P. newelli 12 44 Correct the citation for Pterodroma solandri 2015-A-1 N&MA Classification Committee pp. 423-426 Revise the classification of the Pipridae Background: Our current classification of the Pipridae is as follows: Corapipo altera Chiroxiphia lanceolata Chiroxiphia linearis Xenopipo holochlora Dixiphia pipra Ceratopipra mentalis Ceratopipra erythrocephala Manacus candei Manacus aurantiacus Manacus vitellinus Lepidothrix coronata New information: Ohlson et al. (2013) investigated relationships within the family using DNA sequence data from three nuclear introns and one mitochondrial gene (ND2). They sampled all genera and most species. I have pasted in a screen grab of their tree below. Their results are largely consistent with those of previous studies except for the polyphyly of Chloropipo, members of which are in three parts of the tree. -
Gallo-Cajiao, E., Hamman, E. and B. K. Woodworth. 2020. the International Institutional Framework for Seabird Conservation in the South Pacific
Gallo-Cajiao, E., Hamman, E. and B. K. Woodworth. 2020. The international institutional framework for seabird conservation in the South Pacific. Pp. 93-123. In: Wewerinke-Singh, M. and E. Hamman. (eds). Environmental law and governance in the Pacific: climate change, biodiversity and communities. Routledge Earthscan. New York. 6 The international institutional framework for seabird conservation in the South Pacific Eduardo Gallo- Cajiao, Evan Hamman and Bradley K. Woodworth Introduction The South Pacific region is vitally important for seabirds, yet their conservation is currently at a crossroads.1 Human activities in the marine environment and its surroundings, including the South Pacific, have resulted in multiple threats to this group of birds.2 The scientific literature for conserving seabirds has thus far, and continues to be, primarily focused on the biological dimensions, such as population dynamics, migration, feeding, and breeding ecology.3 In addition, research has been conducted to understand the threats driving their declines, as well as approaches to lessen them (e.g. by-catch mitigation, invasive species eradication).4 While addressing these knowledge gaps is essential to advancing the conservation of seabirds by informing management and policy decisions, researching the governance dimensions, in their own right, is also vitally important. After all, governance is the set of mechanisms that steers society to achieve collective action goals, such as conserving biodiversity, by enabling coordination and cooperation between actors.5 Accordingly, this chapter seeks to contribute to addressing this lacuna by identifying and analysing the inter- 1 CN Jenkins and K Van Houtan, ‘Global and Regional Priorities for Marine Biodiversity Pro- tection’ (2016) 204 Biological Conservation: 333–339. -
Shearwatersrefs V1.10.Pdf
Introduction I have endeavoured to keep typos, errors, omissions etc in this list to a minimum, however when you find more I would be grateful if you could mail the details during 2018 & 2019 to: [email protected]. Please note that this and other Reference Lists I have compiled are not exhaustive and are best employed in conjunction with other sources. Grateful thanks to Ashley Fisher (www.scillypelagics.com) for the cover images. All images © the photographer. Joe Hobbs Index The general order of species follows the International Ornithologists' Union World Bird List (Gill, F. & Donsker, D. (eds.) 2017. IOC World Bird List. Available from: http://www.worldbirdnames.org/ [version 7.3 accessed August 2017]). Version Version 1.10 (January 2018). Cover Main image: Great Shearwater. At sea 3’ SW of the Bishop Rock, Isles of Scilly. 8th August 2009. Picture by Ashley Fisher. Vignette: Sooty Shearwater. At sea off the Isles of Scilly. 14th August 2009. Picture by Ashley Fisher. Species Page No. Audubon's Shearwater [Puffinus lherminieri] 34 Balearic Shearwater [Puffinus mauretanicus] 28 Bannerman's Shearwater [Puffinus bannermani] 37 Barolo Shearwater [Puffinus baroli] 38 Black-vented Shearwater [Puffinus opisthomelas] 30 Boyd's Shearwater [Puffinus boydi] 38 Bryan's Shearwater [Puffinus bryani] 29 Buller's Shearwater [Ardenna bulleri] 15 Cape Verde Shearwater [Calonectris edwardsii] 12 Christmas Island Shearwater [Puffinus nativitatis] 23 Cory's Shearwater [Calonectris borealis] 9 Flesh-footed Shearwater [Ardenna carneipes] 21 Fluttering -
A Checklist of the Birds of Micronesia
A Checklist of the Birds of Micronesia ROBERT P. OWEN Chief Conservationist, Trust Territory of the Pacific Islands Koror, Palau, Caroline Islands 96940 Abstract.-This paper lists 191 species of birds found in Micronesia based on publications on collections and acceptable sight records. The last published checklist of Micronesian birds was published by Baker (1951) and lists 151 species. This present checklist records the English names, scientific names, and geographic localities within Micronesia in which the different species are found, and also gives status information on the birds such as whether resident, migrant or vagrant, and whether introduced, endangered or extinct. The most comprehensive publication on Micronesian birds is that produced by Baker (1951). That publication was based on field work done by Rollin H. Baker and other U. S. military biologists carried out in Micronesia in 1945 and a review of all publications on Micronesian ornithology prior to that date, and up to 1948. In the intervening 29 years, a good many ornithologists and other biologists have traveled or resided in Micronesia for various periods of time and have published accounts of birds seen or collected in Micronesia. Baker (1951) listed 151 full species of birds in Micronesia. The present checklist (Table 1) contains 191 full species. Thus 40 bird species have been added to the list of birds known from Micronesia from published records. Approximately one fourth of the bird species listed in this checklist are based on published sight records. Great care has been used in evaluating published sight records and several have been rejected for one reason or another for inclusion in this publication.