Waterfowl in the Prehistory of South Dakota
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Insular Vertebrate Evolution: the Palaeontological Approach': Monografies De La Societat D'història Natural De Les Balears, Lz: Z05-118
19 DESCRIPTION OF THE SKULL OF THE GENUS SYLVIORNIS POPLIN, 1980 (AVES, GALLIFORMES, SYLVIORNITHIDAE NEW FAMILY), A GIANT EXTINCT BIRD FROM THE HOLOCENE OF NEW CALEDONIA Cécile MOURER-CHAUVIRÉ & Jean Christophe BALOUET MOUREH-CHAUVIRÉ, C. & BALOUET, l.C, zoos. Description of the skull of the genus Syluiornis Poplin, 1980 (Aves, Galliformes, Sylviornithidae new family), a giant extinct bird from the Holocene of New Caledonia. In ALCOVER, J.A. & BaVER, P. (eds.): Proceedings of the International Symposium "Insular Vertebrate Evolution: the Palaeontological Approach': Monografies de la Societat d'Història Natural de les Balears, lZ: Z05-118. Resum El crani de Sylviornismostra una articulació craniarostral completament mòbil, amb dos còndils articulars situats sobre el rostrum, el qual s'insereix al crani en dues superfícies articulars allargades. La presència de dos procesos rostropterigoideus sobre el basisfenoide del rostrum i la forma dels palatins permet confirmar que aquest gènere pertany als Galliformes, però les característiques altament derivades del crani justifiquen el seu emplaçament a una nova família, extingida, Sylviornithidae. El crani de Syluiornis està extremadament eixamplat i dorsoventralment aplanat, mentre que el rostrum és massís, lateralment comprimit, dorsoventralment aixecat i mostra unes cristae tomiales molt fondes. El rostrum exhibeix un ornament ossi gran. La mandíbula mostra una símfisi molt allargada, les branques laterals també presenten unes cristae tomiales fondes, i la part posterior de la mandíbula és molt gruixada. Es discuteix el possible origen i l'alimentació de Syluiornis. Paraules clau: Aves, Galliformes, Extinció, Holocè, Nova Caledònia. Abstract The skull of Syluiornis shows a completely mobile craniorostral articulation, with two articular condyles situated on the rostrum, which insert into two elongated articular surfaces on the cranium. -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
A 2010 Supplement to Ducks, Geese, and Swans of the World
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 20. https://digitalcommons.unl.edu/biosciducksgeeseswans/20 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. The World’s Waterfowl in the 21st Century: A 200 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard Pages xvii–xxiii: recent taxonomic changes, I have revised sev- Introduction to the Family Anatidae eral of the range maps to conform with more current information. For these updates I have Since the 978 publication of my Ducks, Geese relied largely on Kear (2005). and Swans of the World hundreds if not thou- Other important waterfowl books published sands of publications on the Anatidae have since 978 and covering the entire waterfowl appeared, making a comprehensive literature family include an identification guide to the supplement and text updating impossible. -
Avian Premaxilla and Tarsometatarsus from The
762 ShortCommunications andCommentaries [Auk,Vol. 112 The Auk 112(3):762-767, 1995 Avian Premaxilla and Tarsometatarsusfrom the Uppermost Cretaceous of Montana ANDRZEJ ELZANOWSKIa AND MICHAEL K. BRETT-$URMAN2 •Departmentof VertebrateZoology, National Museum of NaturalHistory, SmithsonianInstitution, Washington, D.C. 20560, USA; and 2Departmentof Geology,George Washington University, Washington, D.C. 20052,USA Despitea variety of fragmentary,apparently neog- is rounded and smooth,and the sidesare very steep. nathousavian fossilsknown from the uppermostCre- The largest among the neurovascularforamina scat- taceousdeposits (Brodkorb 1963, Olson 1985, Olson tered on each side are two elongatedorsal foramina: and Parris 1987),we still lack even an approximate the vessel from the rostral one coursed rostrad, whereas idea of how many neognathouslineages survived be- the vesselfrom the caudalone apparentlybifurcated yond the Cretaceous/Tertiaryboundary. Most of the into a smaller rostral and a larger caudal branch. In Maastrichtian avian bones reveal a charadriiform or addition, a number of smaller openingsperforates transitional charadriiform-gruiform morphology, eachside of the symphysis. which may be plesiomorphicfor most (Olson 1985) The ventral surfaceof the premaxillarysymphysis but probably not all of the neognaths(Elzanowski is strongly concave(Fig. lc, d). There are no distinct 1995). Other than that, there is some fossil evidence neurovascularforamina on the ventral (palatal) sur- for the existence of loons in the Cretaceous(Olson face,with the possibleexception of one small opening 1992)and mostly indirect evidencefor the pre-Ter- on the left side. The palatal shelvesof the premaxilla tiary origins of the relict pelecaniforms(Phaethon- begin from the symphysialtip and graduallybroaden tidae and Fregatidae) and procellariiforms (Elza- caudally where each of them occupiesone-third of nowski and Gaiton 1991). -
Appendix, French Names, Supplement
685 APPENDIX Part 1. Speciesreported from the A.O.U. Check-list area with insufficient evidencefor placementon the main list. Specieson this list havebeen reported (published) as occurring in the geographicarea coveredby this Check-list.However, their occurrenceis considered hypotheticalfor one of more of the following reasons: 1. Physicalevidence for their presence(e.g., specimen,photograph, video-tape, audio- recording)is lacking,of disputedorigin, or unknown.See the Prefacefor furtherdiscussion. 2. The naturaloccurrence (unrestrained by humans)of the speciesis disputed. 3. An introducedpopulation has failed to becomeestablished. 4. Inclusionin previouseditions of the Check-listwas basedexclusively on recordsfrom Greenland, which is now outside the A.O.U. Check-list area. Phoebastria irrorata (Salvin). Waved Albatross. Diornedeairrorata Salvin, 1883, Proc. Zool. Soc. London, p. 430. (Callao Bay, Peru.) This speciesbreeds on Hood Island in the Galapagosand on Isla de la Plata off Ecuador, and rangesat seaalong the coastsof Ecuadorand Peru. A specimenwas takenjust outside the North American area at Octavia Rocks, Colombia, near the Panama-Colombiaboundary (8 March 1941, R. C. Murphy). There are sight reportsfrom Panama,west of Pitias Bay, Dari6n, 26 February1941 (Ridgely 1976), and southwestof the Pearl Islands,27 September 1964. Also known as GalapagosAlbatross. ThalassarchechrysosWma (Forster). Gray-headed Albatross. Diornedeachrysostorna J. R. Forster,1785, M6m. Math. Phys. Acad. Sci. Paris 10: 571, pl. 14. (voisinagedu cerclepolaire antarctique & dansl'Ocean Pacifique= Isla de los Estados[= StatenIsland], off Tierra del Fuego.) This speciesbreeds on islandsoff CapeHorn, in the SouthAtlantic, in the southernIndian Ocean,and off New Zealand.Reports from Oregon(mouth of the ColumbiaRiver), California (coastnear Golden Gate), and Panama(Bay of Chiriqu0 are unsatisfactory(see A.O.U. -
The Function and Evolution of the Supraorbital Process in Ducks
THE FUNCTION AND EVOLUTION OF THE SUPRAORBITAL PROCESS IN DUCKS ROBERTJ. RAIKOW THE anteriormargin of the orbit in ducksis formedby the lacrimalbone, which articulateswith the anterolateralmargin of the frontal boneand the posterodorsalcorner of the maxillary processof the nasal bone. The evolu- tion of this bone in birds generally has been dealt with recently by Cracraft (Amer. Midl. Naturalist, 80: 316, 1968), whoseterminology for the parts of the lacrimal bone is followedhere. In many ducksthe postero- dorsalcorner of the lacrimal is marked by a small tubercle,which serves as the site of attachment of the anterior end of the orbital membrane,a sheetof connectivetissue that coversand protectsthe dorsalaspect of the eyeball. In some forms this tubercle has become elongated to form a stout, finger-like projection, the supraorbitalprocess. This appears to provide mechanicalprotection to the eyeball and salt gland (Figure 1). Table 1 lists the occurrenceand degree of developmentof this process in the skulls of all living generaof ducks. CORRELATION WITH FEEDING AND LOCOMOTOR HABITS In the following discussion,data on feeding habits are from Delacour (The waterfowlof the world,vols. 1-3, London,Country Life Ltd., 1954, 1956, 1959). Table 1 showsthat the supraorbital processis developed significantlyonly in certain groupsof ducks that feed underwater. It is absentor rudimentaryin the Tadornini, Cairinini, and Anatini, which are primarily surfacefeeders, but also in Merganetta arma.ta,the Torrent Duck, which feedsunderwater. In the Aythyini it is fairly well-developed in severalspecies of Aythya, which are excellentdivers, but is rudimentary in Netta peposaca,which is moreof a surfacefeeder. It is alsorudimentary in the Canvasback,Aythya valisineria,which dives for vegetation.Among the Mergini the supraorbitalprocess is highly developedin eiders (Poly- sticta, Somateria) , scoters( M elanitta) , and Long-tailed Duck ( Clangula byemalls), all of which feed mainly on invertebratestaken from the bottom. -
Lista Das Aves Do Brasil
90 Annotated checklist of the birds of Brazil by the Brazilian Ornithological Records Committee / Lista comentada das aves do Brasil pelo Comitê Brasileiro de Registros Ornitológicos content / conteÚDO Abstract ............................. 91 Charadriiformes ......................121 Scleruridae .............187 Charadriidae .........121 Dendrocolaptidae ...188 Introduction ........................ 92 Haematopodidae ...121 Xenopidae .............. 195 Methods ................................ 92 Recurvirostridae ....122 Furnariidae ............. 195 Burhinidae ............122 Tyrannides .......................203 Results ................................... 94 Chionidae .............122 Pipridae ..................203 Scolopacidae .........122 Oxyruncidae ..........206 Discussion ............................. 94 Thinocoridae .........124 Onychorhynchidae 206 Checklist of birds of Brazil 96 Jacanidae ...............124 Tityridae ................207 Rheiformes .............................. 96 Rostratulidae .........124 Cotingidae .............209 Tinamiformes .......................... 96 Glareolidae ............124 Pipritidae ............... 211 Anseriformes ........................... 98 Stercorariidae ........125 Platyrinchidae......... 211 Anhimidae ............ 98 Laridae ..................125 Tachurisidae ...........212 Anatidae ................ 98 Sternidae ...............126 Rhynchocyclidae ....212 Galliformes ..............................100 Rynchopidae .........127 Tyrannidae ............. 218 Cracidae ................100 Columbiformes -
Phylogeny and Comparative Ecology of Stiff-Tailed Ducks (Anatidae: Oxyurini)
Wilson Bull., 107(2), 1995, pp. 214-234 PHYLOGENY AND COMPARATIVE ECOLOGY OF STIFF-TAILED DUCKS (ANATIDAE: OXYURINI) BRADLEY C. LIVEZEY’ ABSTRACT.-A cladistic analysis of the stiff-tailed ducks (Anatidae: Oxyurini) was con- ducted using 92 morphological characters. The analysis produced one minimum-length, completely dichotomous phylogenetic tree of high consistency (consistency index for infor- mative characters, 0.74). Monophyly of the tribe was supported by 17 unambiguous syna- pomorphies. Within the tribe, Heteronetta (1 species) is the sister-group of other members; within the latter clade (supported by 2 1 unambiguous synapomorphies), Nomonyx (1 species) is the sister-group of Oxyura (6 species) + Biziura (I species). The latter clade is supported by 10 unambiguous synapomorphies. Monophyly of Oxyuru proper is supported by three unambiguous synapomorphies. All branches in the shortest tree except that uniting Oxyuva, exclusive of jumaicensis, were conserved in a majority-rule consensus tree of 1000 boot- strapped replicates. Biziuru and (to a lesser extent) Heteronetta were highly autapomorphic. Modest evolutionary patterns in body mass, reproductive parameters, and sexual dimorphism are evident, with the most marked, correlated changes occurring in Heteronetta and (es- pecially) Biziura. The implications of these evolutionary trends for reproductive ecology and biogeographic patterns are discussed, and a phylogenetic classification of the tribe is presented. Received 27 April 1994, accepted 10 Nov. 1994. The stiff-tailed ducks (Anatidae: Oxyurini) include some of the most distinctive species of waterfowl; among its members are the only obligate nest-parasite (Black-headed Duck; Heteronetta atricapilla) and the spe- cies showing the greatest sexual size dimorphism (Musk Duck; Biziuru lob&z) in the order Anseriformes (Delacour 1959; Johnsgard 1962, 1978; Weller 1968; Livezey 1986). -
Compendium of Avian Ecology
Compendium of Avian Ecology ZOL 360 Brian M. Napoletano All images taken from the USGS Patuxent Wildlife Research Center. http://www.mbr-pwrc.usgs.gov/id/framlst/infocenter.html Taxonomic information based on the A.O.U. Check List of North American Birds, 7th Edition, 1998. Ecological Information obtained from multiple sources, including The Sibley Guide to Birds, Stokes Field Guide to Birds. Nest and other images scanned from the ZOL 360 Coursepack. Neither the images nor the information herein be copied or reproduced for commercial purposes without the prior consent of the original copyright holders. Full Species Names Common Loon Wood Duck Gaviiformes Anseriformes Gaviidae Anatidae Gavia immer Anatinae Anatini Horned Grebe Aix sponsa Podicipediformes Mallard Podicipedidae Anseriformes Podiceps auritus Anatidae Double-crested Cormorant Anatinae Pelecaniformes Anatini Phalacrocoracidae Anas platyrhynchos Phalacrocorax auritus Blue-Winged Teal Anseriformes Tundra Swan Anatidae Anseriformes Anatinae Anserinae Anatini Cygnini Anas discors Cygnus columbianus Canvasback Anseriformes Snow Goose Anatidae Anseriformes Anatinae Anserinae Aythyini Anserini Aythya valisineria Chen caerulescens Common Goldeneye Canada Goose Anseriformes Anseriformes Anatidae Anserinae Anatinae Anserini Aythyini Branta canadensis Bucephala clangula Red-Breasted Merganser Caspian Tern Anseriformes Charadriiformes Anatidae Scolopaci Anatinae Laridae Aythyini Sterninae Mergus serrator Sterna caspia Hooded Merganser Anseriformes Black Tern Anatidae Charadriiformes Anatinae -
A Molecular Phylogeny of Anseriformes Based on Mitochondrial DNA Analysis
MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution 23 (2002) 339–356 www.academicpress.com A molecular phylogeny of anseriformes based on mitochondrial DNA analysis Carole Donne-Goussee,a Vincent Laudet,b and Catherine Haanni€ a,* a CNRS UMR 5534, Centre de Genetique Moleculaire et Cellulaire, Universite Claude Bernard Lyon 1, 16 rue Raphael Dubois, Ba^t. Mendel, 69622 Villeurbanne Cedex, France b CNRS UMR 5665, Laboratoire de Biologie Moleculaire et Cellulaire, Ecole Normale Superieure de Lyon, 45 Allee d’Italie, 69364 Lyon Cedex 07, France Received 5 June 2001; received in revised form 4 December 2001 Abstract To study the phylogenetic relationships among Anseriformes, sequences for the complete mitochondrial control region (CR) were determined from 45 waterfowl representing 24 genera, i.e., half of the existing genera. To confirm the results based on CR analysis we also analyzed representative species based on two mitochondrial protein-coding genes, cytochrome b (cytb) and NADH dehydrogenase subunit 2 (ND2). These data allowed us to construct a robust phylogeny of the Anseriformes and to compare it with existing phylogenies based on morphological or molecular data. Chauna and Dendrocygna were identified as early offshoots of the Anseriformes. All the remaining taxa fell into two clades that correspond to the two subfamilies Anatinae and Anserinae. Within Anserinae Branta and Anser cluster together, whereas Coscoroba, Cygnus, and Cereopsis form a relatively weak clade with Cygnus diverging first. Five clades are clearly recognizable among Anatinae: (i) the Anatini with Anas and Lophonetta; (ii) the Aythyini with Aythya and Netta; (iii) the Cairinini with Cairina and Aix; (iv) the Mergini with Mergus, Bucephala, Melanitta, Callonetta, So- materia, and Clangula, and (v) the Tadornini with Tadorna, Chloephaga, and Alopochen. -
A North American Stem Turaco, and the Complex Biogeographic History of Modern Birds Daniel J
Field and Hsiang BMC Evolutionary Biology (2018) 18:102 https://doi.org/10.1186/s12862-018-1212-3 RESEARCHARTICLE Open Access A North American stem turaco, and the complex biogeographic history of modern birds Daniel J. Field1,2* and Allison Y. Hsiang2,3 Abstract Background: Earth’s lower latitudes boast the majority of extant avian species-level and higher-order diversity, with many deeply diverging clades restricted to vestiges of Gondwana. However, palaeontological analyses reveal that many avian crown clades with restricted extant distributions had stem group relatives in very different parts of the world. Results: Our phylogenetic analyses support the enigmatic fossil bird Foro panarium Olson 1992 from the early Eocene (Wasatchian) of Wyoming as a stem turaco (Neornithes: Pan-Musophagidae), a clade that is presently endemic to sub-Saharan Africa. Our analyses offer the first well-supported evidence for a stem musophagid (and therefore a useful fossil calibration for avian molecular divergence analyses), and reveal surprising new information on the early morphology and biogeography of this clade. Total-clade Musophagidae is identified as a potential participant in dispersal via the recently proposed ‘North American Gateway’ during the Palaeogene, and new biogeographic analyses illustrate the importance of the fossil record in revealing the complex historical biogeography of crown birds across geological timescales. Conclusions: In the Palaeogene, total-clade Musophagidae was distributed well outside the range of crown Musophagidae in the present day. This observation is consistent with similar biogeographic observations for numerous other modern bird clades, illustrating shortcomings of historical biogeographic analyses that do not incorporate information from the avian fossil record. -
Avian Evolution, Gondwana Biogeography and the Cretaceous
doi 10.1098/rspb.2000.1368 Avian evolution, Gondwana biogeography and the Cretaceous±Tertiary mass extinction event Joel Cracraft Department of Ornithology, American Museum of Natural History, Central Park West at 79th Street, NewYork, NY 10024, USA ( [email protected]) The fossil record has been used to support the origin and radiation of modern birds (Neornithes) in Laurasia after the Cretaceous^Tertiary mass extinction event, whereas molecular clocks have suggested a Cretaceous origin for most avian orders.These alternative views of neornithine evolution are examined using an independent set of evidence, namely phylogenetic relationships and historical biogeography. Phylogenetic relationships of basal lineages of neornithines, including ratite birds and their allies (Palaeognathae), galliforms and anseriforms (Galloanserae), as well as lineages of the more advanced Neoaves (Gruiformes, Caprimulgiformes, Passeriformes and others) demonstrate pervasive trans- Antarctic distribution patterns.The temporal history of the neornithines can be inferred from fossil taxa and the ages of vicariance events, and along with their biogeographical patterns, leads to the conclusion that neornithines arose in Gondwana prior to the Cretaceous^Tertiary extinction event. Keywords: Neornithes; avian evolution; biogeography; Gondwana; Cretaceous^Tertiary extinction marker of neornithine beginnings.The fact that the 1. INTRODUCTION preponderance of the fossils are found in North America The relationships of modern birds, or Neornithes, to non- and Europe is taken as evidence that most higher taxa of avian theropods and Mesozoic pre-neornithine avian birds diversi¢ed on the Laurasian landmass and had lineages, is now well established (Chiappe 1995; Padian little, if anything, to do with Gondwana (Feduccia 1995). & Chiappe 1998; Chiappe et al.