Rangeland Conservation Practices
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6.5 Coastal Cactus Wren (Campylorhynchus Brunneicapillus Sandiegensis) – Category SO Management Units with Known Occurrences
Volume 2D: Goals and Objectives for Species Focus Management Species 6.0 Birds 6.5 Coastal Cactus Wren (Campylorhynchus brunneicapillus sandiegensis) – Category SO Management Units with Known Occurrences Coastal cactus wrens are restricted to cactus-dominated coastal sage scrub habitats in Southern California, from Ventura south to San Diego County and inland to western San Bernardino and western Riverside Counties. These wrens differ ecologically from more common desert wrens in the southwestern United States and northern Mexico. Coastal cactus wrens began significantly declining in San Diego County in the early 1980s due to habitat loss to agriculture and urban development (Rea and Weaver 1990). By 1990 there was a 33% population decline from the previous decade as a result of the loss of coastal birds and smaller populations, and a decline in abundance of remaining populations. Coastal cactus wren surveys and cactus mapping were implemented on Conserved Lands in the MSPA in 2009 and 2011 (USFWS 2011). Cactus wrens were documented on Conserved Lands in MUs 1, 2, 3, 4, 5, and 6 (see Occurrence Table and online map: http://arcg.is/2kU1bka). A range-wide genetics and banding study was conducted across occupied cactus scrub habitats in 2011–2013 by USGS to determine coastal cactus wren population genetic structure, connectivity, and genetic diversity in Southern California (Barr et al. 2015). The study found 3 main genetic clusters in San Diego County: Otay; San Diego/El Cajon (Sweetwater/Encanto/Lake Jennings); and San Pasqual. In the San Diego/El Cajon genetic cluster, wrens in the Sweetwater River watershed are connected to occurrences in Fletcher Hills and Lake Jennings to the northeast in MU4 and to occurrences in Encanto Canyon and other urban canyons to the west in MU2. -
Herpetological Information Service No
Type Descriptions and Type Publications OF HoBART M. Smith, 1933 through June 1999 Ernest A. Liner Houma, Louisiana smithsonian herpetological information service no. 127 2000 SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE The SHIS series publishes and distributes translations, bibliographies, indices, and similar items judged useful to individuals interested in the biology of amphibians and reptiles, but unlikely to be published in the normal technical journals. Single copies are distributed free to interested individuals. Libraries, herpetological associations, and research laboratories are invited to exchange their publications with the Division of Amphibians and Reptiles. We wish to encourage individuals to share their bibliographies, translations, etc. with other herpetologists through the SHIS series. If you have such items please contact George Zug for instructions on preparation and submission. Contributors receive 50 free copies. Please address all requests for copies and inquiries to George Zug, Division of Amphibians and Reptiles, National Museum of Natural History, Smithsonian Institution, Washington DC 20560 USA. Please include a self-addressed mailing label with requests. Introduction Hobart M. Smith is one of herpetology's most prolific autiiors. As of 30 June 1999, he authored or co-authored 1367 publications covering a range of scholarly and popular papers dealing with such diverse subjects as taxonomy, life history, geographical distribution, checklists, nomenclatural problems, bibliographies, herpetological coins, anatomy, comparative anatomy textbooks, pet books, book reviews, abstracts, encyclopedia entries, prefaces and forwords as well as updating volumes being repnnted. The checklists of the herpetofauna of Mexico authored with Dr. Edward H. Taylor are legendary as is the Synopsis of the Herpetofalhva of Mexico coauthored with his late wife, Rozella B. -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. amphibian-reptile-conservation.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
Whistler3 Frontcover
The Whistler is the occasionally issued journal of the Hunter Bird Observers Club Inc. ISSN 1835-7385 The aims of the Hunter Bird Observers Club (HBOC), which is affiliated with Bird Observation and Conservation Australia, are: To encourage and further the study and conservation of Australian birds and their habitat To encourage bird observing as a leisure-time activity HBOC is administered by a Committee: Executive: Committee Members: President: Paul Baird Craig Anderson Vice-President: Grant Brosie Liz Crawford Secretary: Tom Clarke Ann Lindsey Treasurer: Rowley Smith Robert McDonald Ian Martin Mick Roderick Publication of The Whistler is supported by a Sub-committee: Mike Newman (Joint Editor) Harold Tarrant (Joint Editor) Liz Crawford (Production Manager) Chris Herbert (Cover design) Liz Huxtable Ann Lindsey Jenny Powers Mick Roderick Alan Stuart Authors wishing to submit manuscripts for consideration for publication should consult Instructions for Authors on page 61 and submit to the Editors: Mike Newman [email protected] and/or Harold Tarrant [email protected] Authors wishing to contribute articles of general bird and birdwatching news to the club newsletter, which has 6 issues per year, should submit to the Newsletter Editor: Liz Crawford [email protected] © Hunter Bird Observers Club Inc. PO Box 24 New Lambton NSW 2305 Website: www.hboc.org.au Front cover: Australian Painted Snipe Rostratula australis – Photo: Ann Lindsey Back cover: Pacific Golden Plover Pluvialis fulva - Photo: Chris Herbert The Whistler is proudly supported by the Hunter-Central Rivers Catchment Management Authority Editorial The Whistler 3 (2009): i-ii The Whistler – Editorial The Editors are pleased to provide our members hopefully make good reading now, but will and other ornithological enthusiasts with the third certainly provide a useful point of reference for issue of the club’s emerging journal. -
Castle Green Bird List
GREEN CASTLE ESTATE Bird List Birds seen on recent tours during November – April | In one week we can expect around 120 species. E=Endemic | ES=Endemic Subspecies | I=Introduced Some of the species below are very unusual however they have been included for completeness. Jamaica has recorded over 300 species and the birds below are the most frequently encountered, however we cannot guarantee what we will or will not see, that’s birding! West Indian Whistling-Duck Lesser Yellowlegs Greater Antillean Elaenia (ES) Blue-winged Teal Whimbrel Jamaican Pewee (E) Northern Shoveler Ruddy Turnstone Sad Flycatcher (E) Ring-necked Duck Red Knot Rufous-tailed Flycatcher (E) Lesser Scaup Sanderling Stolid Flycatcher (ES) Masked Duck Semipalmated Sandpiper Gray Kingbird Ruddy Duck Western Sandpiper Loggerhead Kingbird (ES) Least Grebe Least Sandpiper Jamaican Becard (E) Pied-billed Grebe White-rumped Sandpiper Jamaican Vireo (E) White-tailed Tropicbird Baird's Sandpiper Blue Mountain Vireo (E) Magnificent Frigatebird Stilt Sandpiper Black-whiskered Vireo Brown Booby Short-billed Dowitcher Jamaican Crow (E) Brown Pelican Laughing Gull Caribbean Martin American Bittern Least Tern Tree Swallow Least Bittern Gull-billed Tern Northern Rough-winged Swallow Great Blue Heron Caspian Tern Cave Swallow (ES) Great Egret Royal Tern Barn Swallow Snowy Egret Sandwich Tern Rufous-throated Solitaire (ES) Little Blue Heron Rock Pigeon (I) White-eyed Thrush (E) Tricolored Heron White-crowned Pigeon White-chinned Thrush (E) Reddish Egret Plain Pigeon (ES) Gray Catbird Cattle -
Campylorhynchus Rufinucha) Rufinucha) (Campylorhynchus
Nest-site characteristics of Rufous-naped Wrens Artículo (Campylorhynchus rufinucha) in Acacia trees may serve to avoid vertebrate predators Características de sitios de los nidos de Campylorhynchus rufinucha en árboles de Acacia posiblemente sirven para evadir depredación por vertebrados Ignacio Escalante1 1Sistema de Estudios de Posgrado, Escuela de Biología, Universidad de Costa Rica. San José, Costa Rica. Ornitología Colombiana Ornitología [email protected] Abstract The high rate of nest predation in tropical birds results in strong selection pressure. The Rufous-naped Wren (Campylorhynchus rufinucha) nests in Bullhorn trees (Acacia) in the Mesoamerican dry forest. It has been proposed that bullhorns and their aggressive ants (Pseudomyrmex spp.) help to prevent nest predation. I tested the hypothesis that these birds place their nests in particular acacia micro- habitats to avoid predation by vertebrates such as tufted capuchin monkeys (Cebus capucinus). I expected to find nests in locations that avoided the foraging behavior preferences of the monkeys. Along 6 km gravel road in Palo Verde National Park, Guanacaste, Costa Rica, I found 52 Rufous-naped Wren nests. The proportion of ant species in acacias with nests did not differ from the background proportion of ant species in acacias without nests, so birds did not prefer to nest in acacias with the most aggressive ant species. Acacia trees with wren nests were larger in diameter than control acacias without nests. I found more nests in acacias that were clustered, which consisted of one to five acacias in a 3m radius plot around the acacia with nest. However, the number of acacias with or without nests did not differ in their isolation from other non-acacia trees. -
REPTILIA: SQUAMATA: PHRYNOSOMATIDAE Sceloporus Poinsettii
856.1 REPTILIA: SQUAMATA: PHRYNOSOMATIDAE Sceloporus poinsettii Catalogue of American Amphibians and Reptiles. Webb, R.G. 2008. Sceloporus poinsettii. Sceloporus poinsettii Baird and Girard Crevice Spiny Lizard Sceloporus poinsettii Baird and Girard 1852:126. Type-locality, “Rio San Pedro of the Rio Grande del Norte, and the province of Sonora,” restricted to either the southern part of the Big Burro Moun- tains or the vicinity of Santa Rita, Grant County, New Mexico by Webb (1988). Lectotype, National Figure 1. Adult male Sceloporus poinsettii poinsettii (UTEP Museum of Natural History (USNM) 2952 (subse- 8714) from the Magdalena Mountains, Socorro County, quently recataloged as USNM 292580), adult New Mexico (photo by author). male, collected by John H. Clark in company with Col. James D. Graham during his tenure with the U.S.-Mexican Boundary Commission in late Au- gust 1851 (examined by author). See Remarks. Sceloporus poinsetii: Duméril 1858:547. Lapsus. Tropidolepis poinsetti: Dugès 1869:143. Invalid emendation (see Remarks). Sceloporus torquatus Var. C.: Bocourt 1874:173. Sceloporus poinsetti: Yarrow “1882"[1883]:58. Invalid emendation. S.[celoporus] t.[orquatus] poinsettii: Cope 1885:402. Seloporus poinsettiii: Herrick, Terry, and Herrick 1899:123. Lapsus. Sceloporus torquatus poinsetti: Brown 1903:546. Sceloporus poissetti: Král 1969:187. Lapsus. Figure 2. Adult female Sceloporus poinsettii axtelli (UTEP S.[celoporus] poinssetti: Méndez-De la Cruz and Gu- 11510) from Alamo Mountain (Cornudas Mountains), tiérrez-Mayén 1991:2. Lapsus. Otero County, New Mexico (photo by author). Scelophorus poinsettii: Cloud, Mallouf, Mercado-Al- linger, Hoyt, Kenmotsu, Sanchez, and Madrid 1994:119. Lapsus. Sceloporus poinsetti aureolus: Auth, Smith, Brown, and Lintz 2000:72. -
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) -
Recommended Band Size List Page 1
Jun 00 Australian Bird and Bat Banding Scheme - Recommended Band Size List Page 1 Australian Bird and Bat Banding Scheme Recommended Band Size List - Birds of Australia and its Territories Number 24 - May 2000 This list contains all extant bird species which have been recorded for Australia and its Territories, including Antarctica, Norfolk Island, Christmas Island and Cocos and Keeling Islands, with their respective RAOU numbers and band sizes as recommended by the Australian Bird and Bat Banding Scheme. The list is in two parts: Part 1 is in taxonomic order, based on information in "The Taxonomy and Species of Birds of Australia and its Territories" (1994) by Leslie Christidis and Walter E. Boles, RAOU Monograph 2, RAOU, Melbourne, for non-passerines; and “The Directory of Australian Birds: Passerines” (1999) by R. Schodde and I.J. Mason, CSIRO Publishing, Collingwood, for passerines. Part 2 is in alphabetic order of common names. The lists include sub-species where these are listed on the Census of Australian Vertebrate Species (CAVS version 8.1, 1994). CHOOSING THE CORRECT BAND Selecting the appropriate band to use combines several factors, including the species to be banded, variability within the species, growth characteristics of the species, and band design. The following list recommends band sizes and metals based on reports from banders, compiled over the life of the ABBBS. For most species, the recommended sizes have been used on substantial numbers of birds. For some species, relatively few individuals have been banded and the size is listed with a question mark. In still other species, too few birds have been banded to justify a size recommendation and none is made. -
The Crimson Finch
PUBLISHED FOR BIRD LOVERS BY BIRD LOVERS life Aviarywww.aviarylife.com.au Issue 04/2015 $12.45 Incl. GST Australia The Red Strawberry Finch Crimson Finch Black-capped Lory One Week in Brazil The Red-breasted Goose ISSN 1832-3405 White-browed Woodswallow The Crimson Finch A Striking Little Aussie! Text by Glenn Johnson Photos by Julian Robinson www.flickr.com/photos/ozjulian/ Barbara Harris www.flickr.com/photos/12539790@N00/ Jon Irvine www.flickr.com/photos/33820263@N07/ and Aviarylife. Introduction he Crimson Finch Neochmia phaeton has Talways been one of the rarer Australian finches in captivity, and even more so since the white- the mid-late 1980’s, when the previously legal bellied. The trapping of wild finches in Australia was crown is dark prohibited across all states. They unfortunately brown, the back and have a bad reputation for being aggressive, wings are paler brown washed with red, the tail and this together with the fact that they is long, scarlet on top and black underneath. are reasonably expensive in comparison to The cheeks along with the entire under parts are many other finches, could well be a couple deep crimson, the flanks are spotted white, and of the main reasons as to why they are not so the centre of the belly is black in the nominate commonly kept. race and white for N. p. evangelinae, and the Description beak is red. Hens are duller, with black beaks. They are an elegant bird, generally standing There are two types of Crimson Finches, the very upright on the perch, and range from 120- black-bellied, which is the nominate form and 140mm in length. -
Predation on Vertebrates by Neotropical Passerine Birds Leonardo E
Lundiana 6(1):57-66, 2005 © 2005 Instituto de Ciências Biológicas - UFMG ISSN 1676-6180 Predation on vertebrates by Neotropical passerine birds Leonardo E. Lopes1,2, Alexandre M. Fernandes1,3 & Miguel Â. Marini1,4 1 Depto. de Biologia Geral, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 31270-910, Belo Horizonte, MG, Brazil. 2 Current address: Lab. de Ornitologia, Depto. de Zoologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Pampulha, 31270-910, Belo Horizonte, MG, Brazil. E-mail: [email protected]. 3 Current address: Coleções Zoológicas, Aves, Instituto Nacional de Pesquisas da Amazônia, Avenida André Araújo, 2936, INPA II, 69083-000, Manaus, AM, Brazil. E-mail: [email protected]. 4 Current address: Lab. de Ornitologia, Depto. de Zoologia, Instituto de Biologia, Universidade de Brasília, 70910-900, Brasília, DF, Brazil. E-mail: [email protected] Abstract We investigated if passerine birds act as important predators of small vertebrates within the Neotropics. We surveyed published studies on bird diets, and information on labels of museum specimens, compiling data on the contents of 5,221 stomachs. Eighteen samples (0.3%) presented evidence of predation on vertebrates. Our bibliographic survey also provided records of 203 passerine species preying upon vertebrates, mainly frogs and lizards. Our data suggest that vertebrate predation by passerines is relatively uncommon in the Neotropics and not characteristic of any family. On the other hand, although rare, the ability to prey on vertebrates seems to be widely distributed among Neotropical passerines, which may respond opportunistically to the stimulus of a potential food item. -
India: Kaziranga National Park Extension
INDIA: KAZIRANGA NATIONAL PARK EXTENSION FEBRUARY 22–27, 2019 The true star of this extension was the Indian One-horned Rhinoceros (Photo M. Valkenburg) LEADER: MACHIEL VALKENBURG LIST COMPILED BY: MACHIEL VALKENBURG VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM INDIA: KAZIRANGA NATIONAL PARK EXTENSION February 22–27, 2019 By Machiel Valkenburg This wonderful Kaziranga extension was part of our amazing Maharajas’ Express train trip, starting in Mumbai and finishing in Delhi. We flew from Delhi to Guwahati, located in the far northeast of India. A long drive later through the hectic traffic of this enjoyable country, we arrived at our lodge in the evening. (Photo by tour participant Robert Warren) We enjoyed three full days of the wildlife and avifauna spectacles of the famous Kaziranga National Park. This park is one of the last easily accessible places to find the endangered Indian One-horned Rhinoceros together with a healthy population of Asian Elephant and Asiatic Wild Buffalo. We saw plenty individuals of all species; the rhino especially made an impression on all of us. It is such an impressive piece of evolution, a serious armored “tank”! On two mornings we loved the elephant rides provided by the park; on the back of these attractive animals we came very close to the rhinos. The fertile flood plains of the park consist of alluvial silts, exposed sandbars, and riverine flood-formed lakes called Beels. This open habitat is not only good for mammals but definitely a true gem for some great birds. Interesting but common birds included Bar-headed Goose, Red Junglefowl, Woolly-necked Stork, and Lesser Adjutant, while the endangered Greater Adjutant and Black-necked Stork were good hits in the stork section.