Phylogenetic and Morphometric Analysis of a New Ornithuromorph from the Barun Goyot Formation, Southern Mongolia
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Flamingo ABOUT the GROUP
Flamingo ABOUT THE GROUP Bulletin of the IUCN-SSC/Wetlands International The Flamingo Specialist Group (FSG) was established in 1978 at Tour du Valat in France, under the leadership of Dr. Alan Johnson, who coordinated the group until 2004 (see profile at www.wetlands.org/networks/Profiles/January.htm). Currently, the group is FLAMINGO SPECIALIST GROUP coordinated from the Wildfowl & Wetlands Trust at Slimbridge, UK, as part of the IUCN- SSC/Wetlands International Waterbird Network. The FSG is a global network of flamingo specialists (both scientists and non- scientists) concerned with the study, monitoring, management and conservation of the world’s six flamingo species populations. Its role is to actively promote flamingo research and conservation worldwide by encouraging information exchange and cooperation amongst these specialists, and with other relevant organisations, particularly IUCN - SSC, Ramsar, WWF International and BirdLife International. FSG members include experts in both in-situ (wild) and ex-situ (captive) flamingo conservation, as well as in fields ranging from field surveys to breeding biology, diseases, tracking movements and data management. There are currently 165 members around the world, from India to Chile, and from France to South Africa. Further information about the FSG, its membership, the membership list serve, or this bulletin can be obtained from Brooks Childress at the address below. Chair Assistant Chair Dr. Brooks Childress Mr. Nigel Jarrett Wildfowl & Wetlands Trust Wildfowl & Wetlands Trust Slimbridge Slimbridge Glos. GL2 7BT, UK Glos. GL2 7BT, UK Tel: +44 (0)1453 860437 Tel: +44 (0)1453 891177 Fax: +44 (0)1453 860437 Fax: +44 (0)1453 890827 [email protected] [email protected] Eastern Hemisphere Chair Western Hemisphere Chair Dr. -
Climatic Shifts Drove Major Contractions in Avian Latitudinal Distributions Throughout the Cenozoic
Climatic shifts drove major contractions in avian latitudinal distributions throughout the Cenozoic Erin E. Saupea,1,2, Alexander Farnsworthb, Daniel J. Luntb, Navjit Sagooc, Karen V. Phamd, and Daniel J. Fielde,1,2 aDepartment of Earth Sciences, University of Oxford, OX1 3AN Oxford, United Kingdom; bSchool of Geographical Sciences, University of Bristol, Clifton, BS8 1SS Bristol, United Kingdom; cDepartment of Meteorology, Stockholm University, 106 91 Stockholm, Sweden; dDivision of Geological and Planetary Sciences, Caltech, Pasadena, CA 91125; and eDepartment of Earth Sciences, University of Cambridge, CB2 3EQ Cambridge, United Kingdom Edited by Nils Chr. Stenseth, University of Oslo, Oslo, Norway, and approved May 7, 2019 (received for review March 8, 2019) Many higher level avian clades are restricted to Earth’s lower lati- order avian historical biogeography invariably recover strong evi- tudes, leading to historical biogeographic reconstructions favoring a dence for an origin of most modern diversity on southern land- Gondwanan origin of crown birds and numerous deep subclades. masses (2, 6, 11). However, several such “tropical-restricted” clades (TRCs) are repre- The crown bird fossil record has unique potential to reveal sented by stem-lineage fossils well outside the ranges of their clos- where different groups of birds were formerly distributed in deep est living relatives, often on northern continents. To assess the time. Fossil evidence, for example, has long indicated that total- drivers of these geographic disjunctions, we combined ecological group representatives of clades restricted to relatively narrow niche modeling, paleoclimate models, and the early Cenozoic fossil geographic regions today were formerly found in different parts of record to examine the influence of climatic change on avian geo- – graphic distributions over the last ∼56 million years. -
Miocene Mammal Reveals a Mesozoic Ghost Lineage on Insular New Zealand, Southwest Pacific
Miocene mammal reveals a Mesozoic ghost lineage on insular New Zealand, southwest Pacific Trevor H. Worthy*†, Alan J. D. Tennyson‡, Michael Archer§, Anne M. Musser¶, Suzanne J. Hand§, Craig Jonesʈ, Barry J. Douglas**, James A. McNamara††, and Robin M. D. Beck§ *School of Earth and Environmental Sciences, Darling Building DP 418, Adelaide University, North Terrace, Adelaide 5005, South Australia, Australia; ‡Museum of New Zealand Te Papa Tongarewa, P.O. Box 467, Wellington 6015, New Zealand; §School of Biological, Earth and Environmental Sciences, University of New South Wales, New South Wales 2052, Australia; ¶Australian Museum, 6-8 College Street, Sydney, New South Wales 2010, Australia; ʈInstitute of Geological and Nuclear Sciences, P.O. Box 30368, Lower Hutt 5040, New Zealand; **Douglas Geological Consultants, 14 Jubilee Street, Dunedin 9011, New Zealand; and ††South Australian Museum, Adelaide, South Australia 5000, Australia Edited by James P. Kennett, University of California, Santa Barbara, CA, and approved October 11, 2006 (sent for review July 8, 2006) New Zealand (NZ) has long been upheld as the archetypical Ma) dinosaur material (13) and isolated moa bones from marine example of a land where the biota evolved without nonvolant sediments up to 2.5 Ma (1, 14), the terrestrial record older than terrestrial mammals. Their absence before human arrival is mys- 1 Ma is extremely limited. Until now, there has been no direct terious, because NZ was still attached to East Antarctica in the Early evidence for the pre-Pleistocene presence in NZ of any of its Cretaceous when a variety of terrestrial mammals occupied the endemic vertebrate lineages, particularly any group of terrestrial adjacent Australian portion of Gondwana. -
Onetouch 4.0 Scanned Documents
/ Chapter 2 THE FOSSIL RECORD OF BIRDS Storrs L. Olson Department of Vertebrate Zoology National Museum of Natural History Smithsonian Institution Washington, DC. I. Introduction 80 II. Archaeopteryx 85 III. Early Cretaceous Birds 87 IV. Hesperornithiformes 89 V. Ichthyornithiformes 91 VI. Other Mesozojc Birds 92 VII. Paleognathous Birds 96 A. The Problem of the Origins of Paleognathous Birds 96 B. The Fossil Record of Paleognathous Birds 104 VIII. The "Basal" Land Bird Assemblage 107 A. Opisthocomidae 109 B. Musophagidae 109 C. Cuculidae HO D. Falconidae HI E. Sagittariidae 112 F. Accipitridae 112 G. Pandionidae 114 H. Galliformes 114 1. Family Incertae Sedis Turnicidae 119 J. Columbiformes 119 K. Psittaciforines 120 L. Family Incertae Sedis Zygodactylidae 121 IX. The "Higher" Land Bird Assemblage 122 A. Coliiformes 124 B. Coraciiformes (Including Trogonidae and Galbulae) 124 C. Strigiformes 129 D. Caprimulgiformes 132 E. Apodiformes 134 F. Family Incertae Sedis Trochilidae 135 G. Order Incertae Sedis Bucerotiformes (Including Upupae) 136 H. Piciformes 138 I. Passeriformes 139 X. The Water Bird Assemblage 141 A. Gruiformes 142 B. Family Incertae Sedis Ardeidae 165 79 Avian Biology, Vol. Vlll ISBN 0-12-249408-3 80 STORES L. OLSON C. Family Incertae Sedis Podicipedidae 168 D. Charadriiformes 169 E. Anseriformes 186 F. Ciconiiformes 188 G. Pelecaniformes 192 H. Procellariiformes 208 I. Gaviiformes 212 J. Sphenisciformes 217 XI. Conclusion 217 References 218 I. Introduction Avian paleontology has long been a poor stepsister to its mammalian counterpart, a fact that may be attributed in some measure to an insufRcien- cy of qualified workers and to the absence in birds of heterodont teeth, on which the greater proportion of the fossil record of mammals is founded. -
SEDIMENTATION of the BARUN GOYOT FORMATION (Plates XXXIV-XLII )
RYSZARD GRADZINSKI & TOMASZ JERZYKIEWICZ SEDIMENTATION OF THE BARUN GOYOT FORMATION (Plates XXXIV-XLII ) Contents C ontents Pa ge Introduction . 112 Geological setting 112 Stratigraphy . .. 114 Previous work .. .. ... .. 114 Redefinition of the lithostratigraphic divisions. 115 Barun Goyot Formation ... 116 Nemegt Formation. .. .. 116 Relation between the observed profiles . 117 Petrographic description . .. 118 Clay and silt-grade sediments 119 Sand-grade sediments . .. 119 Intraformational gravels . 124 Exotic gravels . 124 Principal sediment types . 125 Flat-bedded sandstone units. 125 Mega cross-stratified units . 127 Massive, "structureless" sandstones. 134 Diversely stratified sandstones . 134 Alternating claystones and sandstones 136 Sedimentological interpretation 136 Occurrence of organic remains 140 Depositional environment . 141 Conclusions 143 Appen dix . 143 References . 144 Abstract. - The Barun Goyot Formation (previously termed Lower Nemegt Beds) is composed of clastic continental sediments of red-beds type; it is probably of Campanian age. The thickness of the formation exceeds 110 m. It is overlain by the Nemegt Formation (previously termed Upper Nemegt Beds), probably of Maast richtian age; the passage between the two format ions is gradual. A formal redefinition of the two Iithostra tigraphic divisions is presented in the paper. Five principal sediment types are distinguished in the Barun Goyot Formation, displaying sedimentary features indicative of various conditions of sedimentation. The lower part of the exposed profile of the Barun Goyot Formation is characterized by mega cross-stratified units, interpreted as dune deposits; they are intertonguing with water-deposited sediments laid in interdune areas. Chan nel deposits, attributed to intermittent streams are subordinate; massive sandstones, probably of various origin are predominating. The upper part of the profile of the formation is characterized by the predominance of flat-bedded sandstone units which were probabl y deposited in an intermittently flooded takyr-like area. -
Reidentification of Avian Embryonic Remains from the Cretaceous of Mongolia
RESEARCH ARTICLE Reidentification of Avian Embryonic Remains from the Cretaceous of Mongolia David J. Varricchio1*, Amy M. Balanoff2, Mark A. Norell3 1 Department of Earth Sciences, Montana State University, Bozeman, Montana, 59717, United States of America, 2 Department of Anatomical Sciences, Stony Brook University School of Medicine, Stony Brook, NY, 11794, United States of America, 3 Division of Paleontology, American Museum of Natural History, New York, NY, 10024, United States of America * [email protected] Abstract Embryonic remains within a small (4.75 by 2.23 cm) egg from the Late Cretaceous, Mongo- lia are here re-described. High-resolution X-ray computed tomography (HRCT) was used to digitally prepare and describe the enclosed embryonic bones. The egg, IGM (Mongolian In- stitute for Geology, Ulaanbaatar) 100/2010, with a three-part shell microstructure, was originally assigned to Neoceratopsia implying extensive homoplasy among eggshell char- acters across Dinosauria. Re-examination finds the forelimb significantly longer than the hindlimbs, proportions suggesting an avian identification. Additional, postcranial apomor- phies (strut-like coracoid, cranially located humeral condyles, olecranon fossa, slender radi- OPEN ACCESS us relative to the ulna, trochanteric crest on the femur, and ulna longer than the humerus) identify the embryo as avian. Presence of a dorsal coracoid fossa and a craniocaudally Citation: Varricchio DJ, Balanoff AM, Norell MA (2015) Reidentification of Avian Embryonic Remains compressed distal humerus with a strongly angled distal margin support a diagnosis of IGM from the Cretaceous of Mongolia. PLoS ONE 10(6): 100/2010 as an enantiornithine. Re-identification eliminates the implied homoplasy of this e0128458. doi:10.1371/journal.pone.0128458 tri-laminate eggshell structure, and instead associates enantiornithine birds with eggshell Academic Editor: Peter Dodson, University of microstructure composed of a mammillary, squamatic, and external zones. -
Reported to Have Been Five Or Six Meters High at the Advent of the Present· Residents of the Region
THE TERTIARY LAKE BASIN AT ~FLORISSANT, COLO., BETWEEN SOUTH AND HAYDEN PAHKS.* I [With a map.] By SAMUEL H. SCUDDER. The following remarks are based upon collections. and notes made during a visit to Florissa:qt, in the summer of 1877, in compap.y ·with Messrs. Arthur Lakes, of Golden, Colo., and F. C. Bowditch, of Boston, . Mass. As five days only were spent in the place, most of the time was . given up to the collection and care of specimens, .so that only a general survey of the locality was·possible. Mr. Lakes ·especially gave himself to the· study of the geol9gy of the district, and as he was previously fttrniliar with the structure of the surrounding country, and placed his notes at my disposal, the first part of this paper should be considered our joint production. GEOLOGY. The tertiary lalw basin at Florissant, already famous for its prolific beds of plants and insects, is situated ina narrow valley high up in the mountains at the soethern extremity of the Front Range of Colorado, at no great distance from "Pike's Peak. The first, and, so fat· as I am aware, the only notice of it which has been published, is that lJy Mr. A. C. Peale, in his account of the geology of Hayden Park and the country lying between it and the upper canon of the South Platte. .t As it is brief, it is given here in full: . ''The latter [Beaver Creek] flows to the northwest, and empties into the South Platte just below the upper canon. -
Lyons SCIENCE 2021 the Influence of Juvenile Dinosaurs SUPPL.Pdf
science.sciencemag.org/content/371/6532/941/suppl/DC1 Supplementary Materials for The influence of juvenile dinosaurs on community structure and diversity Katlin Schroeder*, S. Kathleen Lyons, Felisa A. Smith *Corresponding author. Email: [email protected] Published 26 February 2021, Science 371, 941 (2021) DOI: 10.1126/science.abd9220 This PDF file includes: Materials and Methods Supplementary Text Figs. S1 and S2 Tables S1 to S7 References Other Supplementary Material for this manuscript includes the following: (available at science.sciencemag.org/content/371/6532/941/suppl/DC1) MDAR Reproducibility Checklist (PDF) Materials and Methods Data Dinosaur assemblages were identified by downloading all vertebrate occurrences known to species or genus level between 200Ma and 65MA from the Paleobiology Database (PaleoDB 30 https://paleobiodb.org/#/ download 6 August, 2018). Using associated depositional environment and taxonomic information, the vertebrate database was limited to only terrestrial organisms, excluding amphibians, pseudosuchians, champsosaurs and ichnotaxa. Taxa present in formations were confirmed against the most recent available literature, as of November, 2020. Synonymous taxa or otherwise duplicated taxa were removed. Taxa that could not be identified to genus level 35 were included as “Taxon X”. GPS locality data for all formations between 200MA and 65MA was downloaded from PaleoDB to create a minimally convex polygon for each possible formation. Any attempt to recreate local assemblages must include all potentially interacting species, while excluding those that would have been separated by either space or time. We argue it is 40 acceptable to substitute formation for home range in the case of non-avian dinosaurs, as range increases with body size. -
Fossil Birds of the Nebraska Region
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Transactions of the Nebraska Academy of Sciences and Affiliated Societies Nebraska Academy of Sciences 1992 Fossil Birds of the Nebraska Region James E. Ducey [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/tnas Part of the Life Sciences Commons Ducey, James E., "Fossil Birds of the Nebraska Region" (1992). Transactions of the Nebraska Academy of Sciences and Affiliated Societies. 130. https://digitalcommons.unl.edu/tnas/130 This Article is brought to you for free and open access by the Nebraska Academy of Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Transactions of the Nebraska Academy of Sciences and Affiliated Societiesy b an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. 1992. Transactions of the Nebraska Academy of Sciences, XIX: 83-96 FOSSIL BIRDS OF THE NEBRASKA REGION James Ducey 235 Nebraska Hall Lincoln, Nebraska 68588-0521 ABSTRACT Crane (Grus haydeni = Grus canadensis) (Marsh, 1870) and a species of hawk (Buteo dananus) from along the This review compiles published and a few unpublished Loup Fork (Marsh, 1871). records offossil and prehistoric birds for the Nebraska region (Nebraska and parts of adjacent states) from the Cretaceous Many ofthe species first described were from mate Period to the late Pleistocene, about 12,000 years before present. Species recorded during the various epochs include: rial collected in the Great Plains region, including Kan Oligocene and Early Miocene (13 families; 29 species), Middle sas and Wyoming (Marsh, 1872b). The work of scien Miocene (six families; 12 species), Late Miocene (14 families; tists associated with the University of Nebraska in 21 species), Pliocene (six families; 15 species), Early-Middle cluded studies made around the turn-of-the-century. -
Supplementary Information
Supplementary Information Substitution Rate Variation in a Robust Procellariiform Seabird Phylogeny is not Solely Explained by Body Mass, Flight Efficiency, Population Size or Life History Traits Andrea Estandía, R. Terry Chesser, Helen F. James, Max A. Levy, Joan Ferrer Obiol, Vincent Bretagnolle, Jacob González-Solís, Andreanna J. Welch This pdf file includes: Supplementary Information Text Figures S1-S7 SUPPLEMENTARY INFORMATION TEXT Fossil calibrations The fossil record of Procellariiformes is sparse when compared with other bird orders, especially its sister order Sphenisciformes (Ksepka & Clarke 2010, Olson 1985c). There are, however, some fossil Procellariiformes that are both robustly dated and identified and therefore suitable for fossil calibrations. Our justification of these fossils, below, follows best practices described by Parham et al. (2012) where possible. For all calibration points only a minimum age was set with no upper constraint specified, except for the root of the tree. 1. Node between Sphenisciformes/Procellariiformes Minimum age: 60.5 Ma Maximum age: 61.5 Ma Taxon and specimen: Waimanu manneringi (Slack et al. 2006); CM zfa35 (Canterbury Museum, Christchurch, New Zealand), holotype comprising thoracic vertebrae, caudal vertebrae, pelvis, femur, tibiotarsus, and tarsometatarsus. Locality: Basal Waipara Greensand, Waipara River, New Zealand. Phylogenetic justification: Waimanu has been resolved as the basal penguin taxon using morphological data (Slack et al. 2006), as well as combined morphological and molecular datasets (Ksepka et al. 2006, Clarke et al. 2007). Morphological and molecular phylogenies agree on the monophyly of Sphenisciformes and Procellariiformes (Livezey & Zusi 2007, Prum et al. 2015). Waimanu manneringi was previously used by Prum et al. (2015) to calibrate Sphenisiciformes, and see Ksepka & Clarke (2015) for a review of the utility of this fossil as a robust calibration point. -
Saurolophus Angustirostris (Dinosauria: Hadrosauridae), from the Upper Cretaceous of Mongolia
RESEARCH ARTICLE Perinatal Specimens of Saurolophus angustirostris (Dinosauria: Hadrosauridae), from the Upper Cretaceous of Mongolia Leonard Dewaele1,2*, Khishigjav Tsogtbaatar3, Rinchen Barsbold3, Géraldine Garcia4, Koen Stein5, François Escuillié6, Pascal Godefroit1 1 Directorate 'Earth and History of Life', Royal Belgian Institute of Natural Sciences, rue Vautier 29, B-1000, Brussels, Belgium, 2 Research Unit Palaeontology, Department Geology and Soil Sciences, Ghent University, Krijgslaan 281, 9000, Ghent, Belgium, 3 Institute of Paleontology and Geology, Mongolian Academy of Sciences, Ulaanbaatar, 210–351, Mongolia, 4 Université de Poitiers, IPHEP, UMR CNRS 7262, 6 rue M. Brunet, 86073, Poitiers cedex 9, France, 5 Earth System Science, AMGC, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium, 6 Eldonia, 9 Avenue des Portes Occitanes, 3800, Gannat, France * [email protected] OPEN ACCESS Abstract Citation: Dewaele L, Tsogtbaatar K, Barsbold R, Garcia G, Stein K, Escuillié F, et al. (2015) Perinatal Specimens of Saurolophus angustirostris Background (Dinosauria: Hadrosauridae), from the Upper The Late Cretaceous Nemegt Formation, Gobi Desert, Mongolia has already yielded abun- Cretaceous of Mongolia. PLoS ONE 10(10): dant and complete skeletons of the hadrosaur Saurolophus angustirostris, from half-grown e0138806. doi:10.1371/journal.pone.0138806 to adult individuals. Editor: Andrew A. Farke, Raymond M. Alf Museum of Paleontology, UNITED STATES Received: April 22, 2015 Methodology/Principal Findings Accepted: September 3, 2015 Herein we describe perinatal specimens of Saurolophus angustirostris, associated with fragmentary eggshell fragments. The skull length of these babies is around 5% that of the Published: October 14, 2015 largest known S. angustirostris specimens, so these specimens document the earliest Copyright: © 2015 Dewaele et al. -
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.