Mammals and Birds Petition
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
First Confirmed Breeding Record of Plume-Toed Swiftlet Collocalia Affinis in Singapore
BirdingASIA 31 (2019)(2019): 85–87 85 BREEDING RECORD First confirmed breeding record of Plume-toed Swiftlet Collocalia affinis in Singapore ALFRED CHIA, DING LI YONG, KIM CHUAH LIM, MOVIN NYANASENGERAN, YONG CHEE KEITA SIN, KIM KEANG LIM & SENG BENG YEO Historically the tiny Collocalia swiftlets resident In the meantime, the results of a detailed in both the lowlands and higher altitudes of analysis of the taxonomy of Collocalia swiftlets in Peninsular Malaysia were designated Glossy the Indo-Pacific region (Rheindt et al. 2017) led to Swiftlet C. esculenta cyanoptila (Wells 1999). the proposal of radical changes to the established However, the species was rare on Singapore taxonomy; this was a big challenge due to the mainland, with fewer than 10 records per year, all morphological uniformity of these taxa. Rheindt apparently in the period November to February, et al. (2017) studied the evolutionary history of the which is the non-breeding season in Malaysia complex, combining new biometric measurements (Wells 1999). In recent times the frequency of and plumage assessment of museum specimens records in Singapore has increased, including a with novel as well as previously published group of up to seven birds at Bukit Batok Nature molecular data, with a total of 809 individuals Park in January 2005, as well as regular records representative of 32 taxa being assessed. The thereafter in and at the periphery of the Central authors propose changing the classification of Nature Reserves, and its status was revised to white-bellied swiftlets, for which just two species ‘uncommon’ (Yong et al. 2017, Lim 2018). -
Territory Size and Stability in a Sedentary Neotropical Passerine: Is Resource Partitioning a Necessary Condition?
J. Field Ornithol. 76(4):395±401, 2005 Territory size and stability in a sedentary neotropical passerine: is resource partitioning a necessary condition? Janet V. Gorrell,1 Gary Ritchison,1,3 and Eugene S. Morton2 1 Department of Biological Sciences, Eastern Kentucky University, Richmond, Kentucky 40475 USA 2 Hemlock Hill Field Station, 22318 Teepleville Flats Road, Cambridge Springs, Pennsylvania 16403 USA Received 9 April 2004; accepted 11 April 2005 ABSTRACT. Long-term pair bonds and defense of territories year-round are common among tropical passer- ines. The boundaries of these territories tend to be stable, perhaps re¯ecting the need to defend an area that, regardless of conditions, provides suf®cient food resources. If, however, these stable territories are not, even tem- porarily, suf®ciently large, then intra-pair competition for available food may result, particularly in species with no sexual size dimorphism. With such competition, sex-speci®c differences in foraging behavior may result. Male and female Dusky Antbirds (Cercomacra tyrannina) are not size dimorphic, and pairs jointly defend territories throughout the year. Our objective was to determine if paired Dusky Antbirds exhibited sex-speci®c differences in foraging behavior. Foraging antbirds were observed in central Panama from February±July 2002 to determine if pairs par- titioned food resources. Males and females exhibited no differences in foraging behavior, with individuals of both sexes foraging at similar heights and using the same foraging maneuvers (glean, probe, and sally) and substrates (leaves, rolled leaves, and woody surfaces). These results suggest that Dusky Antbirds do not partition resources and that territory switching, rather than resource partitioning, may be the means by which they gain access to additional food resources. -
Bird Checklist Guánica Biosphere Reserve Puerto Rico
United States Department of Agriculture BirD CheCklist Guánica Biosphere reserve Puerto rico Wayne J. Arendt, John Faaborg, Miguel Canals, and Jerry Bauer Forest Service Research & Development Southern Research Station Research Note SRS-23 The Authors: Wayne J. Arendt, International Institute of Tropical Forestry, U.S. Department of Agriculture Forest Service, Sabana Field Research Station, HC 2 Box 6205, Luquillo, PR 00773, USA; John Faaborg, Division of Biological Sciences, University of Missouri, Columbia, MO 65211-7400, USA; Miguel Canals, DRNA—Bosque de Guánica, P.O. Box 1185, Guánica, PR 00653-1185, USA; and Jerry Bauer, International Institute of Tropical Forestry, U.S. Department of Agriculture Forest Service, Río Piedras, PR 00926, USA. Cover Photos Large cover photograph by Jerry Bauer; small cover photographs by Mike Morel. Product Disclaimer The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. April 2015 Southern Research Station 200 W.T. Weaver Blvd. Asheville, NC 28804 www.srs.fs.usda.gov BirD CheCklist Guánica Biosphere reserve Puerto rico Wayne J. Arendt, John Faaborg, Miguel Canals, and Jerry Bauer ABSTRACt This research note compiles 43 years of research and monitoring data to produce the first comprehensive checklist of the dry forest avian community found within the Guánica Biosphere Reserve. We provide an overview of the reserve along with sighting locales, a list of 185 birds with their resident status and abundance, and a list of the available bird habitats. Photographs of habitats and some of the bird species are included. -
Checklist of the Birds of Christmas Island and Cocos (Keeling) Islands
Checklist of the Birds of Christmas Island and Cocos (Keeling) Islands Christmas Island Emerald Dove feathers R.E. Johnstone and J.C. Darnell Collections and Research, Western Australian Museum, Kew Street, Welshpool, WA 6106 †June 2021 ____________________________________ This checklist covers Christmas and Cocos (Keeling) Islands in the tropical eastern Indian Ocean and their surrounding seas. Christmas Island lies 290 km south of Java (Indonesia) and 1,400 km north-west of Western Australia. It is a small uplifted volcanic island (137 km² in area) and is administered by Western Australia as an External Territory of Australia. The Cocos (Keeling) Islands lie 970 km west of Christmas Island and 2,100 km north-west of Western Australia. They comprise two low-lying atolls, a large southern atoll (Cocos) consisting of about 26 islands around a horseshoe-shaped lagoon and a smaller North Keeling Island lying 25 km to the north. They cover a land area of about 14 km² and are also administered by Western Australia as an External Territory of Australia. The main aim of this work is to provide an up-to-date checklist of the birds of this region to include the large number of additional species that have been recorded on these islands since the publication of the Annotated Checklists of Christmas Island and Cocos (Keeling) Islands in 2004 (Johnstone and Darnell Appendix A and B in: Handbook of Western Australian Birds Volume II) and the more recent review of the birds of Christmas Island (James and McAllan 2014 Australian Field Ornithology Suppl. 31). Criterion for inclusion of a species or subspecies on the list is, in most cases, supported by tangible evidence i.e. -
Pacific Sheath-Tailed Bat American Samoa Emballonura Semicaudata Semicaudata Species Report April 2020
Pacific Sheath-tailed Bat American Samoa Emballonura semicaudata semicaudata Species Report April 2020 U.S. Fish and Wildlife Service Pacific Islands Fish and Wildlife Office Honolulu, HI Cover Photo Credits Shawn Thomas, Bat Conservation International. Suggested Citation USFWS. 2020. Species Status Assessment for the Pacific Sheath Tailed Bat (Emballonura semicaudata semicaudata). April 2020 (Version 1.1). U.S. Fish and Wildlife Service, Pacific Islands Fish and Wildlife Office, Honolulu, HI. 57 pp. Primary Authors Version 1.1 of this document was prepared by Mari Reeves, Fred Amidon, and James Kwon of the Pacific Islands Fish and Wildlife Office, Honolulu, Hawaii. Preparation and review was conducted by Gregory Koob, Megan Laut, and Stephen E. Miller of the Pacific Islands Fish and Wildlife Office. Acknowledgements We thank the following individuals for their contribution to this work: Marcos Gorresen, Adam Miles, Jorge Palmeirim, Dave Waldien, Dick Watling, and Gary Wiles. ii Executive Summary This Species Report uses the best available scientific and commercial information to assess the status of the semicaudata subspecies of the Pacific sheath-tailed bat, Emballonura semicaudata semicaudata. This subspecies is found in southern Polynesia, eastern Melanesia, and Micronesia. Three additional subspecies of E. semicaudata (E.s. rotensis, E.s. palauensis, and E.s. sulcata) are not discussed here unless they are used to support assumptions about E.s. semicaudata, or to fill in data gaps in this analysis. The Pacific sheath-tailed bat is an Old-World bat in the family Emballonuridae, and is found in parts of Polynesia, eastern Melanesia, and Micronesia. It is the only insectivorous bat recorded from much of this area. -
The Usefulness of Taped Spotless Crake Calls As a Census Technique
682 THE WILSON BULLETIN l Vol. 100, No. 4, December1988 motory systems suggeststhat subtle differences among species ’ center of gravity may explain the adaptive significance of interspecific differences in head-scratching method. Acknowledgments.-We thank C. Blem and two anonymous referees for their helpful comments on an earlier draft. LITERATURE CITED AMEIUCAN ORNITHOLOGISTS' UNION. 1983. Check-list of North American Birds, 6th ed. A.O.U., Washington, D.C. BURTT, E. H., JR. 1977. Some factors in the timing of parent-chick recognition in swallows. Anim. Behav. 25:231-239. -. 1980. Overwing and underwing head-scratching by a male Black and White War- bler Mniotilta varia. Ibis 122:54 1. -. 1983. Head-scratching method of Galapagos finches unaffected by variation in cranial morphology. Wilson Bull. 95: 158-160. -AND J. P. HAILMAN. 1978. Head-scratching among North American Wood-Warblers (Parulidae). Ibis 120:153-170. DUNHAM, D. W. 1963. Head-scratching in the Hairy Woodpecker, Dendrocoposvillosus. Auk 80~375. HEINROTH, 0. 19 17. Reflektorische Bewegungsweisen (Kratzen, Schutteln, Baden u.s.w.) im Lichte der stammesverwandschaft. J. Omithol. 66:ll l-l 14. -. 1930. Uber bestimmte Bewegungsweisen von Wirbeltierren. Sitzungsber. Ges. Naturf Freunde Berlin:333-342. LORENZ, K. Z. 1950. The comparative method in studying innate behaviour patterns. Symp. Sot. Exp. Biol. 4:221-268. MAYFIELD, H. 1960. The Kirtlands’ Warbler. Cranbrook Institute of Science, Bloomfield Hills, Michigan. MEYER DE SCHAUENSEE,R. 1970. A guide to the birds of South America. Livingston Publishing Co., Wynnewood, Pennsylvania. SIMMONS, K. E. L. 1961. Problems of head-scratching in birds. Ibis 103:37-49. -
Wetland Restoration Handbook Chapter 11 Pests
CHAPTER 11 PESTS CORINNE WATTS AND MONICA PETERS CONTENTS INTRODUCTION 1 RESTORING YOUR WETLAND 1.1 Developing a Wetland Restoration Plan 1.1.1 Mapping 1.2 Determining wetland type 1.3 Understanding the site 1.4 Setting realistic goals and objectives 1.4.1 Keeping it legal 2 TERRESTRIAL AND AQUATIC WETLAND PESTS 2.1 Control or eradication? 3 PEST ANIMALS 3.1 Selecting appropriate control methods 3.1.1 Poisoning, trapping or shooting? 3.1.2 Repellents 4 PEST FISH 4.1 Control 4.2 Eradication 5 MONITORING 5.1 5-minute bird counts 5.2 Wax tags 5.3 Tracking tunnels 5.4 Foliar browse 5.5 Fish trapping 6 REFERENCES AND FURTHER READING 6.1 Useful websites SECTION TWO: ACTION ON THE GROUND CHAPTER 11 PESTS 185 PESTS WETLAND RESTORATION: A HANDBOOK FOR NZ FRESHWATER SYSTEMS PESTS CORINNE WATTS AND MONICA PETERS Since the human colonization of New Zealand all eat invertebrates, birds’ eggs, chicks and even began, many new animals have arrived. Some adult birds. Introduced browsing animals, e.g., species have been intentionally introduced – the possums, goats, rabbits, hares and cattle eat Australian brushtail possum for the fur trade, and native vegetation and will target recent plantings stoats to kill previously introduced rabbits that of nursery-grown plants as they provide rich had begun to reach plague proportions. Others sources of nutrients. In addition, rats will devour have arrived unintentionally, often as stowaways seeds that are so important for seedbanks. To a on boats. Irrespective of the method of arrival, the lesser extent, dogs may harass wetland birds. -
The Birds (Aves) of Oromia, Ethiopia – an Annotated Checklist
European Journal of Taxonomy 306: 1–69 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.306 www.europeanjournaloftaxonomy.eu 2017 · Gedeon K. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:A32EAE51-9051-458A-81DD-8EA921901CDC The birds (Aves) of Oromia, Ethiopia – an annotated checklist Kai GEDEON 1,*, Chemere ZEWDIE 2 & Till TÖPFER 3 1 Saxon Ornithologists’ Society, P.O. Box 1129, 09331 Hohenstein-Ernstthal, Germany. 2 Oromia Forest and Wildlife Enterprise, P.O. Box 1075, Debre Zeit, Ethiopia. 3 Zoological Research Museum Alexander Koenig, Centre for Taxonomy and Evolutionary Research, Adenauerallee 160, 53113 Bonn, Germany. * Corresponding author: [email protected] 2 Email: [email protected] 3 Email: [email protected] 1 urn:lsid:zoobank.org:author:F46B3F50-41E2-4629-9951-778F69A5BBA2 2 urn:lsid:zoobank.org:author:F59FEDB3-627A-4D52-A6CB-4F26846C0FC5 3 urn:lsid:zoobank.org:author:A87BE9B4-8FC6-4E11-8DB4-BDBB3CFBBEAA Abstract. Oromia is the largest National Regional State of Ethiopia. Here we present the first comprehensive checklist of its birds. A total of 804 bird species has been recorded, 601 of them confirmed (443) or assumed (158) to be breeding birds. At least 561 are all-year residents (and 31 more potentially so), at least 73 are Afrotropical migrants and visitors (and 44 more potentially so), and 184 are Palaearctic migrants and visitors (and eight more potentially so). Three species are endemic to Oromia, 18 to Ethiopia and 43 to the Horn of Africa. 170 Oromia bird species are biome restricted: 57 to the Afrotropical Highlands biome, 95 to the Somali-Masai biome, and 18 to the Sudan-Guinea Savanna biome. -
View Preprint
Does evolution of plumage patterns and of migratory behaviour in Apodini swifts (Aves: Apodiformes) follow distributional range shifts? Dieter Thomas Tietze, Martin Päckert, Michael Wink The Apodini swifts in the Old World serve as an example for a recent radiation on an intercontinental scale on the one hand. On the other hand they provide a model for the interplay of trait and distributional range evolution with speciation, extinction and trait s t transition rates on a low taxonomic level (23 extant taxa). Swifts are well adapted to a life n i mostly in the air and to long-distance movements. Their overall colouration is dull, but r P lighter feather patches of chin and rump stand out as visual signals. Only few Apodini taxa e r breed outside the tropics; they are the only species in the study group that migrate long P distances to wintering grounds in the tropics and subtropics. We reconstructed a dated molecular phylogeny including all species, numerous outgroups and fossil constraints. Several methods were used for historical biogeography and two models for the study of trait evolution. We finally correlated trait expression with geographic status. The differentiation of the Apodini took place in less than 9 Ma. Their ancestral range most likely comprised large parts of the Old-World tropics, although the majority of extant taxa breed in the Afrotropic and the closest relatives occur in the Indomalayan. The expression of all three investigated traits increased speciation rates and the traits were more likely lost than gained. Chin patches are found in almost all species, so that no association with phylogeny or range could be found. -
Literature Cited Proposed Critical Habitat Designation for Elfin-Woods Warbler (EWWA), Setophaga Angelae
Literature Cited Proposed Critical Habitat Designation for Elfin-woods Warbler (EWWA), Setophaga angelae Abt Associates, Inc. 2016. Screening analysis of the likely economic impacts of critical habitat designation for the elfin-woods warbler. March 7, 2016 memo to U.S. Fish and Wildlife Service. Aide, T. M. and M. Campos. 2016. Elfin-woods warbler acoustic monitoring. Preliminary report: Carite. Prepared for U.S. Fish and Wildlife Service. 10 pp. Anadón-Irizarry, V. 2006. Distribution, habitat occupancy and population density of the elfin-woods warbler (Dendroica angelae) in Puerto Rico. Master’s Thesis. University of Puerto Rico, Mayagüez Campus. 53 pp. Anadón-Irizarry, V. 2014. Personal communication regarding the searching for a third population of the elfin-woods warbler. Caribbean Program Manager, Birdlife International Inc. E-mail: November 10, 2014. Arendt, W.J., S.S. Qian, and K.A. Mineard. 2013. Population decline of the elfin-woods warbler Setophaga angelae in eastern Puerto Rico. Bird Conservation International, Birdlife International 2013. 11 pp. Arroyo-Vázquez, B. 1992. Observations of the breeding biology of the elfin-woods warbler. Wilson Bulletin 104:362-365. Colón-Merced, R. 2013. Evaluación cuantitativa de presas potenciales, tipo artrópodo, y análisis paisajista del hábitat potencial para la Reinita de Bosque Enano (Setophaga angelae) en Puerto Rico. Master’s Thesis. University of Puerto Rico, Mayagüez Campus. 126 pp. Delannoy, C.A. 2007. Distribution, abundance and description of habitats of the elfin- woods warbler Dendroica angelae, in southwestern Puerto Rico. Final Report submitted to the U.S. Fish and Wildlife Service under Grant Agreement No. 401814G078. University of Puerto Rico, Mayagüez Campus. -
BIRD CONSERVATION the Magazine of American Bird Conservancy Fall 2012 BIRD’S EYE VIEW
BIRD CONSERVATION The Magazine of American Bird Conservancy Fall 2012 BIRD’S EYE VIEW Is Species Conservation Enough? How should we as conservationists decide which birds deserve protection? Where should we draw the line that tells us which groups of birds are “unique” enough to merit saving? t one extreme, a conserva- becomes extinct? Do we care about tion skeptic might insist that the continuation of these evolution- Apreserving one type of bird ary processes, or do we take a pass from each genus is sufficient. At the on preserving them because these other, passionate lovers of wildlife birds are not sufficiently “unique”? may not accept the loss of even one When in doubt about whether to individual. A more typical birder take conservation action, I fall back might nominate the species as the on the precautionary principle, key conservation level because the which says, in essence, that when concept of species is familiar to us. l American Dipper: USFWS uncertain about the potential harm- Science gets us closer to the answers, ful effect of an action, the prudent but it cannot draw the line: the purpose of science is course is the conservative one. or, as aldo Leopold to gather knowledge, not to make decisions for us. wrote, “Save all of the pieces.” Furthermore, like life itself, the science of taxonomy is I say, save the Black Hills Dipper regardless of which in a constant state of change. Baltimore and Bullock’s taxonomic opinion prevails; and while we are at it, we Orioles have been “lumped” into Northern Oriole and ought to save Wayne’s Warbler, the rhododendron- then “split” again, all based on the most current scien- dwelling Swainson’s Warbler, and the tree-nesting tific opinion. -
The All-Bird Bulletin
Advancing Integrated Bird Conservation in North America Spring 2014 Inside this issue: The All-Bird Bulletin Protecting Habitat for 4 the Buff-breasted Sandpiper in Bolivia The Neotropical Migratory Bird Conservation Conserving the “Jewels 6 Act (NMBCA): Thirteen Years of Hemispheric in the Crown” for Neotropical Migrants Bird Conservation Guy Foulks, Program Coordinator, Division of Bird Habitat Conservation, U.S. Fish and Bird Conservation in 8 Wildlife Service (USFWS) Costa Rica’s Agricultural Matrix In 2000, responding to alarming declines in many Neotropical migratory bird popu- Uruguayan Rice Fields 10 lations due to habitat loss and degradation, Congress passed the Neotropical Migra- as Wintering Habitat for tory Bird Conservation Act (NMBCA). The legislation created a unique funding Neotropical Shorebirds source to foster the cooperative conservation needed to sustain these species through all stages of their life cycles, which occur throughout the Western Hemi- Conserving Antigua’s 12 sphere. Since its first year of appropriations in 2002, the NMBCA has become in- Most Critical Bird strumental to migratory bird conservation Habitat in the Americas. Neotropical Migratory 14 Bird Conservation in the The mission of the North American Bird Heart of South America Conservation Initiative is to ensure that populations and habitats of North Ameri- Aros/Yaqui River Habi- 16 ca's birds are protected, restored, and en- tat Conservation hanced through coordinated efforts at in- ternational, national, regional, and local Strategic Conservation 18 levels, guided by sound science and effec- in the Appalachians of tive management. The NMBCA’s mission Southern Quebec is to achieve just this for over 380 Neo- tropical migratory bird species by provid- ...and more! Cerulean Warbler, a Neotropical migrant, is a ing conservation support within and be- USFWS Bird of Conservation Concern and listed as yond North America—to Latin America Vulnerable on the International Union for Conser- Coordination and editorial vation of Nature (IUCN) Red List.