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A Preliminary Reassessment of Philippine Species-Level Bird Taxonomy
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by KU ScholarWorks Bird Conservation International (2006) 16:155–173. BirdLife International 2006 doi:10.1017/S0959270906000256 Printed in the United Kingdom Taxonomy is important in conservation: a preliminary reassessment of Philippine species-level bird taxonomy A. TOWNSEND PETERSON SummarySummarySummary Alpha taxonomy involves delineation of the basic unit of biology: the species. The concepts by which we define species, however, have been controversial, with several alternatives competing at present, some creating fewer and some more species units, depending on interpretation of species limits. Although it is tempting to assume that species concepts would have little inter- action with the geographic foci of species richness and endemism — and some have so argued — this assumption does not withstand careful analysis. In this paper, I develop a first-pass assessment of Philippine bird taxonomy under an alternative species concept, and compare the results with the traditional biological species concept lists. Differences between the two lists were dramatic, but not just in numbers of species; rather, new, previously unrecognized or previously underappreciated foci of endemism were noted. A thorough understanding of the taxonomic basis of species lists is therefore critical to conservation planning. Introduction Recent taxonomic studies have pointed out conservation implications of their results for several parts of the world (Boon et al. 2000; Lovette et al. 1999; Ortíz-Pulido et al. 2002): new viewpoints on species limits led to new priorities for conservation action, mainly via recognition of ‘new’ (although not necessarily undescribed) species-level taxa. -
Labile Evolution of Display Traits in Bowerbirds Indicates Reduced Effects of Phylogenetic Constraint
Labile evolution of display traits in bowerbirds indicates reduced effects of phylogenetic constraint " # # RAB KUSMIERSKI , GERALD BORGIA , ALBERT UY " ROSS H.CROZIER " School of Genetics and Human Variation, La Trobe Uniersit, Bundoora, Victoria 3083, Australia # Department of Zoolog, Uniersit of Marland, College Park, MD 20742, USA SUMMARY Bowerbirds (Ptilonorhynchidae) have among the most exaggerated sets of display traits known, including bowers, decorated display courts and bright plumage, that differ greatly in form and degree of elaboration among species. Mapping bower and plumage traits on an independently derived phylogeny constructed from mitochondrial cytochrome b sequences revealed large differences in display traits between closely related species and convergences in both morphological and behavioural traits. Plumage characters showed no effect of phylogenetic inertia, although bowers exhibited some constraint at the more fundamental level of design, but above which they appeared free of constraint. Bowers and plumage characters, therefore, are poor indicators of phylogenetic relationship in this group. Testing Gilliard’s (1969) transferral hypothesis indicated some support for the idea that the focus of display has shifted from bird to bower in avenue-building species, but not in maypole-builders or in bowerbirds as a whole. maypole-builders (Amblornis, four spp.; Prionodura) in- 1. INTRODUCTION clude the orange-crested males of A. macgregoriae, which Bowerbirds (Ptilonorhynchidae) form a monophyletic decorate a sapling with horizontally interwoven sticks. family (Kusmierski et al. 1993) (eight genera, 19 species) The dull-coloured, monomorphic A. inornatus of endemic to Australia and New Guinea, and are unique western Irian Jaya (Arfak and Wandamen mountains) in the bird world in constructing and using a bower in and the orange-crested, dimorphic A. -
The Megapode Action Plan 1995 - 1999 Halfway Down the Road
ZV-327-13 (pp 151-158) 02-01-2007 15:24 Pagina 151 The megapode action plan 1995 - 1999 halfway down the road R.W.R.J. Dekker Dekker, R.W.R.J. The megapode action plan 1995 - 1999 halfway down the road. René W.R.J. Dekker, National Museum of Natural History, P.O. Box 9517, 2300 RA Leiden, The Netherlands. E-mail: [email protected] Key words: Megapodiidae; megapodes; action plan; conservation; current projects; IUCN threat cate- gories. Megapodes: an action plan for their conservation 1995 - 1999, a collaborative effort of members of the Megapode Specialist Group and the World Pheasant Association, was published in 1995. It summa- rizes the conservation status of all megapode taxa and indicates the needs of those species under threat. The Action Plan was intended to be a stimulus for conservation orientated studies and to gen- erate funds more easily. An overview is given of studies (1990 - present) in which these threatened taxa were involved. The status of these and other taxa are reassessed according to the finalized IUCN threat categories (which supercede the Mace-Lande threat categories originally used in the Action Plan) as a preparation for the megapode action plan 2000 - 2004. Introduction Megapodes: an action plan for their conservation 1995 - 1999 (Dekker & McGowan, 1995) was published by the Species Survival Commission (SSC) of the International Union for the Conservation of Nature (IUCN) in 1995 following a Conservation Assessment Management Plan (CAMP) meeting on galliforms held in Antwerp, Bel- gium, in February 1993. The megapode action plan, soon followed by action plans for partridges, quails, francolins, snowcocks and guineafowl (McGowan et al., 1995) and pheasants (McGowan & Garson, 1995), was the first avian action plan published by the IUCN in their series of conservation action plans. -
Disaggregation of Bird Families Listed on Cms Appendix Ii
Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2. -
PAPUA NEW GUINEA Paradise Untamed
Tropical Birding: Papua New Guinea July-August 2010 A Tropical Birding Set Departure Tour PAPUA NEW GUINEA (with the NEW BRITAIN EXTENSION): Paradise Untamed RIBBON-TAILED ASTRAPIA Kumul Lodge Voted bird of the trip 15 July – 5 August, 2010 Tour Leader: Sam Woods www.tropicalbirding.com [email protected] 1-409-515-0514 1 Tropical Birding: Papua New Guinea July-August 2010 Papua New Guinea is known as the “land of unexpected”, and their national saying is “expect the unexpected”. For good, and bad, we experienced some examples of this during this successful tour on this resource-rich island, and ammased a great trip list of 407 species . Some of what we saw was very much expected: a slew of species from arguably the most spectacular bird family on the planet, the outrageous birds-of-paradise. We picked up 24 species of birds-of-paradise on the tour, with the majority being males, some of which were seen in full, jaw-dropping display mode! The flurry of displaying male Greater Birds-of-paradise during a late afternoon show in the steamy lowland jungle near Kiunga standing out, as did the wonderful performance put on by PNG’s national bird, the Raggiana Bird-of- paradise near the nation’s capital, at Varirata NP. Getting a bunch of BOPs was expected, even in the land of the unexpected. However, on only our third day in the country watching a tree full of BOPs, of NINE different species (and 3 sicklebill species at one time in the same tree ) was very much unexpected even in New Guinea. -
Management and Breeding of Birds of Paradise (Family Paradisaeidae) at the Al Wabra Wildlife Preservation
Management and breeding of Birds of Paradise (family Paradisaeidae) at the Al Wabra Wildlife Preservation. By Richard Switzer Bird Curator, Al Wabra Wildlife Preservation. Presentation for Aviary Congress Singapore, November 2008 Introduction to Birds of Paradise in the Wild Taxonomy The family Paradisaeidae is in the order Passeriformes. In the past decade since the publication of Frith and Beehler (1998), the taxonomy of the family Paradisaeidae has been re-evaluated considerably. Frith and Beehler (1998) listed 42 species in 17 genera. However, the monotypic genus Macgregoria (MacGregor’s Bird of Paradise) has been re-classified in the family Meliphagidae (Honeyeaters). Similarly, 3 species in 2 genera (Cnemophilus and Loboparadisea) – formerly described as the “Wide-gaped Birds of Paradise” – have been re-classified as members of the family Melanocharitidae (Berrypeckers and Longbills) (Cracraft and Feinstein 2000). Additionally the two genera of Sicklebills (Epimachus and Drepanornis) are now considered to be combined as the one genus Epimachus. These changes reduce the total number of genera in the family Paradisaeidae to 13. However, despite the elimination of the 4 species mentioned above, 3 species have been newly described – Berlepsch's Parotia (P. berlepschi), Eastern or Helen’s Parotia (P. helenae) and the Eastern or Growling Riflebird (P. intercedens). The Berlepsch’s Parotia was once considered to be a subspecies of the Carola's Parotia. It was previously known only from four female specimens, discovered in 1985. It was rediscovered during a Conservation International expedition in 2005 and was photographed for the first time. The Eastern Parotia, also known as Helena's Parotia, is sometimes considered to be a subspecies of Lawes's Parotia, but differs in the male’s frontal crest and the female's dorsal plumage colours. -
The Avifauna of Mt. Karimui, Chimbu Province, Papua New Guinea, Including Evidence for Long-Term Population Dynamics in Undisturbed Tropical Forest
Ben Freeman & Alexandra M. Class Freeman 30 Bull. B.O.C. 2014 134(1) The avifauna of Mt. Karimui, Chimbu Province, Papua New Guinea, including evidence for long-term population dynamics in undisturbed tropical forest Ben Freeman & Alexandra M. Class Freeman Received 27 July 2013 Summary.—We conducted ornithological feld work on Mt. Karimui and in the surrounding lowlands in 2011–12, a site frst surveyed for birds by J. Diamond in 1965. We report range extensions, elevational records and notes on poorly known species observed during our work. We also present a list with elevational distributions for the 271 species recorded in the Karimui region. Finally, we detail possible changes in species abundance and distribution that have occurred between Diamond’s feld work and our own. Most prominently, we suggest that Bicolored Mouse-warbler Crateroscelis nigrorufa might recently have colonised Mt. Karimui’s north-western ridge, a rare example of distributional change in an avian population inhabiting intact tropical forests. The island of New Guinea harbours a diverse, largely endemic avifauna (Beehler et al. 1986). However, ornithological studies are hampered by difculties of access, safety and cost. Consequently, many of its endemic birds remain poorly known, and feld workers continue to describe new taxa (Prat 2000, Beehler et al. 2007), report large range extensions (Freeman et al. 2013) and elucidate natural history (Dumbacher et al. 1992). Of necessity, avifaunal studies are usually based on short-term feld work. As a result, population dynamics are poorly known and limited to comparisons of diferent surveys or diferences noticeable over short timescales (Diamond 1971, Mack & Wright 1996). -
Predictable Evolution Toward Flightlessness in Volant Island Birds
Predictable evolution toward flightlessness in volant island birds Natalie A. Wrighta,b,1, David W. Steadmanc, and Christopher C. Witta aDepartment of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM 87131-0001; bDivision of Biological Sciences, University of Montana, Missoula, MT 59812; and cFlorida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800 Edited by James A. Estes, University of California, Santa Cruz, CA, and approved March 9, 2016 (received for review November 19, 2015) Birds are prolific colonists of islands, where they readily evolve distinct predators (18). Alternatively, flightlessness may represent an ex- forms. Identifying predictable, directional patterns of evolutionary treme state of a continuum of morphological variation that reflects change in island birds, however, has proved challenging. The “island locomotory requirements for survival and reproduction. Across a rule” predicts that island species evolve toward intermediate sizes, but continuum of insularity, from continents to small islands, biotic its general applicability to birds is questionable. However, convergent communities exhibit gradients of species diversity (21) and corre- evolution has clearly occurred in the island bird lineages that have sponding ecological pressures (22). If flightlessness is illustrative of undergone transitions to secondary flightlessness, a process involving island bird evolution in general, reductions in predation pressure drastic reduction of the flight muscles and enlargement of the hin- associated with increased insularity should trigger incremental shifts dlimbs. Here, we investigated whether volant island bird populations in energy allocation from the forelimbs to the hindlimbs. Accord- tend to change shape in a way that converges subtly on the flightless ingly, we hypothesize that volant island birds, even those unlikely to form. -
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. -
Australian Field Ornithology, Volume 32: Index
Australian Field Ornithology 2015, 32, 211–224 Australian Field Ornithology, Volume 32: Index INDEX OF ARTICLES Bird community in the Pilliga Forests, New South Wales, between 1918 and 2004, Changes in the ........................................................................................... 118 Bird community, The, of an Acacia-dominated secondary rainforest: A brief case study ............................................................................................................. 59 Crow, Torresian, Corvus orru, Exploring possible functions of vocalisations in the .............................................................................................. 201 Cuckoo, Long-tailed, A recent specimen of a, from Lord Howe Island ................. 53 D. L. Serventy Medal 2015: Citation - Stephen J. S. Debus ................................... 167 Eagles, Wedge-tailed, Aquila audax, Observations of the killing of large macropods by ....................................................................................................... 160 Editorial: A new look, new platform and new era for Australian Field Ornithology from 2016 ........................................................................................ 57 Fantail, Dimorphic, Rhipidura brachyrhyncha, Nest and egg of the, and a review of clutch-sizes in New Guinean passerines .............................................. 69 Frigatebird, Christmas, Fregata andrewsi in the Northern Territory, Australia, Additional records of .......................................................................................... -
Two New Species of Paraphilopterus Mey, 2004 (Phthiraptera: Ischnocera: Philopteridae)
Zootaxa 3873 (2): 155–164 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3873.2.3 http://zoobank.org/urn:lsid:zoobank.org:pub:D78B845A-99D8-423E-B520-C3DD83E3C87F Two new species of Paraphilopterus Mey, 2004 (Phthiraptera: Ischnocera: Philopteridae) from New Guinean bowerbirds (Passeriformes: Ptilonorhynchidae) and satinbirds (Passeriformes: Cnemophilidae) DANIEL R. GUSTAFSSON1,2 & SARAH E. BUSH1 1Department of Biology, University of Utah, 257 S. 1400 E., Salt Lake City, Utah, 84112, USA 2Corresponding author. E-mail: [email protected] Abstract Two new species of Paraphilopterus Mey, 2004 are described and named. Paraphilopterus knutieae n. sp. is described from two subspecies of Macgregor's bowerbirds: Amblyornis macgregoriae nubicola Schodde & McKean, 1973 and A. m. kombok Schodde & McKean, 1973, and Sanford's bowerbird: Archboldia sanfordi (Mayr & Gilliard, 1950) (Ptilono- rhynchidae). Paraphilopterus meyi n. sp. is described from two subspecies of crested satinbirds: Cnemophilus macgrego- rii macgregorii De Vis, 1890 and C. m. sanguineus Iredale, 1948 (Cnemophilidae). These new louse species represent the first records of the genus Paraphilopterus outside Australia, as well as from host families other than the Corcoracidae. The description of Paraphilopterus is revised and expanded based on the additional new species, including the first de- scription of the male of this genus. Also, we provide a key to the species of Paraphilopterus. Key words: Phthiraptera, Ischnocera, Philopteridae, Paraphilopterus, chewing lice, new species, Ptilonorhynchidae, Cnemophilidae, New Guinea Introduction Mey (2004: 188) described the new genus Paraphilopterus based on a single female louse from the Australian host Corcorax melanoramphos (Vieillot, 1817) (Corcoracidae). -
A Classification of the Rallidae
A CLASSIFICATION OF THE RALLIDAE STARRY L. OLSON HE family Rallidae, containing over 150 living or recently extinct species T and having one of the widest distributions of any family of terrestrial vertebrates, has, in proportion to its size and interest, received less study than perhaps any other major group of birds. The only two attempts at a classifi- cation of all of the recent rallid genera are those of Sharpe (1894) and Peters (1934). Although each of these lists has some merit, neither is satisfactory in reflecting relationships between the genera and both often separate closely related groups. In the past, no attempt has been made to identify the more primitive members of the Rallidae or to illuminate evolutionary trends in the family. Lists almost invariably begin with the genus Rdus which is actually one of the most specialized genera of the family and does not represent an ancestral or primitive stock. One of the difficulties of rallid taxonomy arises from the relative homo- geneity of the family, rails for the most part being rather generalized birds with few groups having morphological modifications that clearly define them. As a consequence, particularly well-marked genera have been elevated to subfamily rank on the basis of characters that in more diverse families would not be considered as significant. Another weakness of former classifications of the family arose from what Mayr (194933) referred to as the “instability of the morphology of rails.” This “instability of morphology,” while seeming to belie what I have just said about homogeneity, refers only to the characteristics associated with flightlessness-a condition that appears with great regularity in island rails and which has evolved many times.