Proposal to Amend the Appendices I Or II for CITES Cop16
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CIRCULAR 153 MAY 1967 OBSERVATIONS on SPECIES of CYPRESS INDIGENOUS to the UNITED STATES Agricultural Experiment Station AUBURN UNIVERSIT Y E. V. Smith, Director Auburn, Alabama CONTENTS Page SPECIES AND VARIETIES OF CUPRESSUS STUDIED 4 GEOGRAPHIC DISTRIBUTION-- 4 CONE COLLECTION 5 Cupressus arizonica var. arizonica (Arizona Cypress) 7 Cupressus arizonica var. glabra (Smooth Arizona Cypress) 11 Cupressus guadalupensis (Tecate Cypress) 11 Cupressus arizonicavar. stephensonii (Cuyamaca Cypress) 11 Cupressus sargentii (Sargent Cypress) 12 Cupressus macrocarpa (Monterey Cypress) 12 Cupressus goveniana (Gowen Cypress) 12 Cupressus goveniana (Santa Cruz Cypress) 12 Cupressus goveniana var. pygmaca (Mendocino Cypress) 12 Cupressus bakeri (Siskiyou Cypress) 13 Cupressus bakeri (Modoc Cypress) 13 Cupressus macnabiana (McNab Cypress) 13 Cupressus arizonica var. nevadensis (Piute Cypress) 13 GENERAL COMMENTS ON GEOGRAPHIC VARIATION ---------- 13 COMMENTS ON STUDYING CYPRESSES 19 FIRST PRINTING 3M, MAY 1967 OBSERVATIONS on SPECIES of CYPRESS INDIGENOUS to the UNITED STATES CLAYTON E. POSEY* and JAMES F. GOGGANS Department of Forestry THERE HAS BEEN considerable interest in growing Cupressus (cypress) in the Southeast for several years. The Agricultural Experiment Station, Auburn University, was the first institution in the Southeast to initiate work on the cy- presses in 1937, and since that time many states have introduced Cupressus in hope of finding a species suitable for Christmas tree production. In most cases seed for trial plantings were obtained from commercial dealers without reference to seed source or form of parent tree. Many plantings yielded a high proportion of columnar-shaped trees not suitable for the Christmas tree market. It is probable that seed used in Alabama and other Southeastern States came from only a few trees of a given geo- graphic source. -
Vol 29 #2.Final
Cypress forest on Guadalupe Island showing signs of goat herbivory. The islets Toro and Zapato are in the far distance. All photographs courtesy of Island Conservation unless otherwise noted. THE RESTORATION OF GUADALUPE ISLAND by Bradford Keitt, Steve Junak, Luciana Luna Mendoza, and Alfonso Aguirre “Guadalupe is remarkable for ende- ing an extensive lichen flora and ing across the island in our own mism in the flora and fauna; but it is a important remnants of unique cloud of dust and exhaust, we’ve naturalist’s paradise despoiled by feral coastal scrub and island chaparral also wondered what lures us back goats, housecats, and mice. [The island] communities. year after year. Yet, just as the bar- is a Mexican national treasure in dire Guadalupe stirs a love-hate re- ren beauty of Guadalupe and the need of protection” (Moran 1996). lationship in those that have come excitement of finding rare and ex- to know its sere, rugged landscape. otic plants seduced Dr. Moran, we uadalupe Island rises like a Botanist Reid Moran, whose 40 too are captivated by the island’s Grampart from the wind- years of work on Guadalupe brought ecosystem. For that reason, we have whipped sea off the Pacific attention to its unique flora, called committed ourselves to protecting coast of the Baja California Penin- it his “very favorite island,” but he and restoring the remaining pock- sula. As the westernmost territory mused that “at too close a range it ets of its unique flora and fauna in Mexico, the 26,000 hectare is- has sometimes seemed a hot, ugly, with the hope that the island can land is a lonely outpost for a small weedy, insuperable rock pile that I eventually recover some of its origi- military garrison and a community have almost wondered, at least fleet- nal biodiversity. -
Chromosome Numbers in Gymnosperms - an Update
Rastogi and Ohri . Silvae Genetica (2020) 69, 13 - 19 13 Chromosome Numbers in Gymnosperms - An Update Shubhi Rastogi and Deepak Ohri Amity Institute of Biotechnology, Research Cell, Amity University Uttar Pradesh, Lucknow Campus, Malhaur (Near Railway Station), P.O. Chinhat, Luc know-226028 (U.P.) * Corresponding author: Deepak Ohri, E mail: [email protected], [email protected] Abstract still some controversy with regard to a monophyletic or para- phyletic origin of the gymnosperms (Hill 2005). Recently they The present report is based on a cytological data base on 614 have been classified into four subclasses Cycadidae, Ginkgoi- (56.0 %) of the total 1104 recognized species and 82 (90.0 %) of dae, Gnetidae and Pinidae under the class Equisetopsida the 88 recognized genera of gymnosperms. Family Cycada- (Chase and Reveal 2009) comprising 12 families and 83 genera ceae and many genera of Zamiaceae show intrageneric unifor- (Christenhusz et al. 2011) and 88 genera with 1104 recognized mity of somatic numbers, the genus Zamia is represented by a species according to the Plant List (www.theplantlist.org). The range of number from 2n=16-28. Ginkgo, Welwitschia and Gen- validity of accepted name of each taxa and the total number of tum show 2n=24, 2n=42, and 2n=44 respectively. Ephedra species in each genus has been checked from the Plant List shows a range of polyploidy from 2x-8x based on n=7. The (www.theplantlist.org). The chromosome numbers of 688 taxa family Pinaceae as a whole shows 2n=24except for Pseudolarix arranged according to the recent classification (Christenhusz and Pseudotsuga with 2n=44 and 2n=26 respectively. -
La Brea and Beyond: the Paleontology of Asphalt-Preserved Biotas
La Brea and Beyond: The Paleontology of Asphalt-Preserved Biotas Edited by John M. Harris Natural History Museum of Los Angeles County Science Series 42 September 15, 2015 Cover Illustration: Pit 91 in 1915 An asphaltic bone mass in Pit 91 was discovered and exposed by the Los Angeles County Museum of History, Science and Art in the summer of 1915. The Los Angeles County Museum of Natural History resumed excavation at this site in 1969. Retrieval of the “microfossils” from the asphaltic matrix has yielded a wealth of insect, mollusk, and plant remains, more than doubling the number of species recovered by earlier excavations. Today, the current excavation site is 900 square feet in extent, yielding fossils that range in age from about 15,000 to about 42,000 radiocarbon years. Natural History Museum of Los Angeles County Archives, RLB 347. LA BREA AND BEYOND: THE PALEONTOLOGY OF ASPHALT-PRESERVED BIOTAS Edited By John M. Harris NO. 42 SCIENCE SERIES NATURAL HISTORY MUSEUM OF LOS ANGELES COUNTY SCIENTIFIC PUBLICATIONS COMMITTEE Luis M. Chiappe, Vice President for Research and Collections John M. Harris, Committee Chairman Joel W. Martin Gregory Pauly Christine Thacker Xiaoming Wang K. Victoria Brown, Managing Editor Go Online to www.nhm.org/scholarlypublications for open access to volumes of Science Series and Contributions in Science. Natural History Museum of Los Angeles County Los Angeles, California 90007 ISSN 1-891276-27-1 Published on September 15, 2015 Printed at Allen Press, Inc., Lawrence, Kansas PREFACE Rancho La Brea was a Mexican land grant Basin during the Late Pleistocene—sagebrush located to the west of El Pueblo de Nuestra scrub dotted with groves of oak and juniper with Sen˜ora la Reina de los A´ ngeles del Rı´ode riparian woodland along the major stream courses Porciu´ncula, now better known as downtown and with chaparral vegetation on the surrounding Los Angeles. -
Syringeal Morphology and the Phylogeny of the Falconidae’
The Condor 96:127-140 Q The Cooper Ornithological Society 1994 SYRINGEAL MORPHOLOGY AND THE PHYLOGENY OF THE FALCONIDAE’ CAROLES.GRIFFITHS Departmentof Ornithology,American Museum of NaturalHistory and Departmentef Biology, City Collegeof City Universityof New York, Central Park West at 79th St., New York, NY 10024 Abstract. Variation in syringealmorphology was studied to resolve the relationshipsof representativesof all of the recognized genera of falcons, falconets, pygmy falcons, and caracarasin the family Falconidae. The phylogenyderived from thesedata establishesthree major cladeswithin the family: (1) the Polyborinae, containingDaptrius, Polyborus, Milvago and Phalcoboenus,the four genera of caracaras;(2) the Falconinae, consistingof the genus Falco, Polihierax (pygmy falcons),Spiziapteryx and Microhierax (falconets)and Herpetothe- res (Laughing Falcon); and (3) the genus Micrastur(forest falcons) comprising the third, basal clade. Two genera, Daptriusand Polihierax,are found to be polyphyletic. The phy- logeny inferred from these syringealdata do not support the current division of the family into two subfamilies. Key words: Falconidae;phylogeny; systematics; syrinx; falcons; caracaras. INTRODUCTION 1. The Polyborinae. This includes seven gen- Phylogenetic relationships form the basis for re- era: Daptrius, Milvago, Polyborus and Phalco- searchin comparative and evolutionary biology boenus(the caracaras),Micrastur (forest falcons), (Page1 and Harvey 1988, Gittleman and Luh Herpetotheres(Laughing Falcon) and Spiziapter- 1992). Patterns drawn from cladogramsprovide yx (Spot-winged Falconet). the blueprints for understanding biodiversity, 2. The Falconinae. This includes three genera: biogeography,behavior, and parasite-hostcospe- Falco, Polihierax (pygmy falcons) and Micro- ciation (Vane-Wright et al. 199 1, Mayden 1988, hierax (falconets). Page 1988, Coddington 1988) and are one of the Inclusion of the caracarasin the Polyborinae key ingredients for planning conservation strat- is not questioned (Sharpe 1874, Swann 1922, egies(Erwin 199 1, May 1990). -
CITES Cop16 Prop. 14 IUCN-TRAFFIC Analysis (PDF, 67KB)
Ref. CoP16 Prop. 14 Deletion of Guadalupe Caracara Caracara lutosa from Appendix II Proponent: Mexico Summary: The Guadalupe Caracara Caracara lutosa was a falcon endemic to the 240 km2 Guadalupe Island in the Gulf of California, Mexico. It was described in 1875 but by 1889 it was thought to have been extirpated from the island as a result of persecution from local goat farmers protecting their livestock through poisoning and hunting. However, eleven individuals were reportedly collected in 1900. A survey in 1906 failed to locate a single individual, and more recent surveys through the 20th century have found no individuals. The species is classified on the IUCN Red List as Extinct. Caracara lutosa was listed in Appendix II in 1975 as part of the listing for all Falconiformes, of which all species are included in either Appendix I or II except for Sarcoramphus papa, listed in Appendix III by Honduras in 1987. The Guadalupe Caracara was one of three species in the genus Caracara¸ and was similar in appearance to the two others Caracara cheriway (Northern Crested Caracara) and Caracara plancus (Southern Crested Caracara), both extremely widespread birds in the Americas, neither of which is considered threatened. There has been some trade in Caracara plancus with 323 live birds reported as exported since 1977, around 14% of these being reported as hatched or bred in captivity. Minimal trade has been recorded for Caracara cheriway since 2008 (one live, one captive-bred body and four scientific specimens). In the highly unlikely event of the species being rediscovered it would be protected by Mexican legislation under the Ley General de Vida Silvestre which would only authorize the use of specimens of species at risk when prioritizing collection and capture for restoration activities, restocking and reintroduction. -
Crested Caracara in Arizona: Background & Recent Expansion
Arizona Birds - Journal of Arizona Field Ornithologists Volume 2015 CRESTED CARACARA IN ARIZONA: BACKGROUND & RECENT EXPANSION DOUG JENNESS, 4375 E. Rollins Rd., Tucson, AZ 85739, [email protected] ABSTRACT: This paper reviews the research history on the Crested Caracara (Caracara cheriway) in Arizona and summarizes the current knowledge of caracara distribution, which shows that caracaras are expanding in the state. I show that part of this expansion is reflected by new field observations and data documenting nesting northeast of its previously known breeding territory, as well as the extent of nonbreeding caracaras to wander and socially forage in the state. The Crested Caracara (Caracara cheriway; Fig 1), a unique member of the falconidae, is found in the southern United States, parts of Mexico and Central America, northern South America, and Cuba (Ferguson-Lees and Christie 2001). In the United States it breeds in central Florida, the southwestern corner of Louisiana, southern Texas, and southern Arizona (Morrison and Dwyer 2012, Wheeler 2003). Caracaras in Louisiana, Texas, and Arizona are contiguous with breeding populations in Mexico. The Florida population is isolated and has been classified as threatened by state and federal governments since 1987 (Morrison and Dwyer 2012). In 1986, the Arizona Game and Fish Department (AZGFD) contracted Levy to conduct a “status survey” of the Crested Caracara in Arizona with funds from Section 6 of the Endangered Species Act (fide R. Glinski). This three- Figure 1: Adult Crested Caracara at Santa Cruz Flats, year study, conducted on the Tohono O’odham Nation, Pinal Co., Arizona, 29 November 2013. Photo by Muriel remains the principal source for our understanding of Neddermeyer caracara breeding behavior in Arizona. -
The Raptor Chimango Caracara (Milvago Chimango) (Aves
IJP: Parasites and Wildlife 10 (2019) 310–313 Contents lists available at ScienceDirect IJP: Parasites and Wildlife journal homepage: www.elsevier.com/locate/ijppaw The raptor Chimango Caracara (Milvago chimango) (Aves: Falconiformes) - A new host for Trichomonas gallinae (protozoa: Trichomonadidae) T ∗ Mirian Pinheiro Brunia, , Joanna Vargas Zillig Echeniqueb, Carolina Caetano dos Santosa, Marcia Raquel Pegoraro de Macedoa, Paulo Mota Bandarrad, Cláudio Dias Timmc, Ana Lúcia Pereira Schilde, Jerônimo Lopes Ruase, Mauro Pereira Soarese, Nara Amélia da Rosa Fariasa a Biology Institute, Federal University of Pelotas (UFPel), Pelotas, Brazil b Department of Veterinary Pathology, College of Veterinary Medicine, Federal University of Rio Grande do Sul, Porto Alegre, Brazil c School of Medicine Veterinary, Federal University of Pelotas (UFPel), Pelotas, Brazil d Wildlife Rehabilitation Center and Wild Animals Triage Center - NURFS/CETAS, Pelotas, Brazil e Regional Veterinary Diagnosis Laboratory, School of Veterinary Medicine, Federal University of Pelotas (UFPel), Pelotas, Brazil ARTICLE INFO ABSTRACT Keywords: This work describes a specimen of Chimango Caracara (Milvago chimango - Vieillot, 1816), from southern Brazil, Raptors as a new natural host for Trichomonas gallinae (Rivolta, 1878). Caseous oral lesions were observed in a young Falcons bird, and the parasite was isolated in modified Diamond’s media. Morphology of the parasite was evaluated Trichomonosis through microscopy and subsequently, sequencing of the internal transcribed spacer 1 (ITS1) of ribosomal DNA Avian diseases was performed to confirm T. gallinae identification. As far as authors are concerned, this is the first report of Milvago chimango as a natural host for T. gallinae. 1. Introduction impaired feeding and drinking, in addition to excessive salivation. -
2020 National Bird List
2020 NATIONAL BIRD LIST See General Rules, Eye Protection & other Policies on www.soinc.org as they apply to every event. Kingdom – ANIMALIA Great Blue Heron Ardea herodias ORDER: Charadriiformes Phylum – CHORDATA Snowy Egret Egretta thula Lapwings and Plovers (Charadriidae) Green Heron American Golden-Plover Subphylum – VERTEBRATA Black-crowned Night-heron Killdeer Charadrius vociferus Class - AVES Ibises and Spoonbills Oystercatchers (Haematopodidae) Family Group (Family Name) (Threskiornithidae) American Oystercatcher Common Name [Scientifc name Roseate Spoonbill Platalea ajaja Stilts and Avocets (Recurvirostridae) is in italics] Black-necked Stilt ORDER: Anseriformes ORDER: Suliformes American Avocet Recurvirostra Ducks, Geese, and Swans (Anatidae) Cormorants (Phalacrocoracidae) americana Black-bellied Whistling-duck Double-crested Cormorant Sandpipers, Phalaropes, and Allies Snow Goose Phalacrocorax auritus (Scolopacidae) Canada Goose Branta canadensis Darters (Anhingidae) Spotted Sandpiper Trumpeter Swan Anhinga Anhinga anhinga Ruddy Turnstone Wood Duck Aix sponsa Frigatebirds (Fregatidae) Dunlin Calidris alpina Mallard Anas platyrhynchos Magnifcent Frigatebird Wilson’s Snipe Northern Shoveler American Woodcock Scolopax minor Green-winged Teal ORDER: Ciconiiformes Gulls, Terns, and Skimmers (Laridae) Canvasback Deep-water Waders (Ciconiidae) Laughing Gull Hooded Merganser Wood Stork Ring-billed Gull Herring Gull Larus argentatus ORDER: Galliformes ORDER: Falconiformes Least Tern Sternula antillarum Partridges, Grouse, Turkeys, and -
Gene Duplications and Genomic Conflict Underlie Major Pulses of Phenotypic 2 Evolution in Gymnosperms 3 4 Gregory W
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.13.435279; this version posted March 15, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 1 Gene duplications and genomic conflict underlie major pulses of phenotypic 2 evolution in gymnosperms 3 4 Gregory W. Stull1,2,†, Xiao-Jian Qu3,†, Caroline Parins-Fukuchi4, Ying-Ying Yang1, Jun-Bo 5 Yang2, Zhi-Yun Yang2, Yi Hu5, Hong Ma5, Pamela S. Soltis6, Douglas E. Soltis6,7, De-Zhu Li1,2,*, 6 Stephen A. Smith8,*, Ting-Shuang Yi1,2,*. 7 8 1Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, 9 Kunming, Yunnan, China. 10 2CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of 11 Botany, Chinese Academy of Sciences, Kunming, China. 12 3Shandong Provincial Key Laboratory of Plant Stress Research, College of Life Sciences, 13 Shandong Normal University, Jinan, Shandong, China. 14 4Department of Geophysical Sciences, University of Chicago, Chicago, IL, USA. 15 5Department of Biology, Huck Institutes of the Life Sciences, Pennsylvania State University, 16 University Park, PA, USA. 17 6Florida Museum of Natural History, University of Florida, Gainesville, FL, USA. 18 7Department of Biology, University of Florida, Gainesville, FL, USA. 19 8Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, 20 MI, USA. 21 †Co-first author. 22 *Correspondence to: [email protected]; [email protected]; [email protected]. -
Cupressus Pygmaea Is a Valid Species
Bull. CCP 1 (2): 27-33 J. Bisbee & D. Mаеrki Cupressus pygmaea (Lemmon) Sargent 1901 Cupressus pygmaea is a valid species In 1895 Lemmon described a new taxon from Mendocino County, and recognising its affinity with Cupressus goveniana Gordon (1849), but with enough differences to separate it from the later, he described it as a variety Cupressus goveniana var. pigmaea 1. Six years later, considering the tiny black seeds and that the isolation of the region which it inhabits remote from that occupied by other Species make it possible and convenient to separate this northern tree from the Cupressus Goveniana of central and southern California, Sargent (1901) raised this taxon to specific rank as Cupressus pygmaea 2. C.B.Wolf (1948) acknowledged this view and stressed the fact that it is necessary and possible to look for distinct characters not visible on dry herbarium material. E.Little (1953) chose to reduce several new world Cupressus species to synonymy. Cupressus pygmaea, Cupressus abramsiana Wolf and Cupressus sargentii Jepson were simply merged into Cupressus goveniana 3 and given as synonyms. In 1970, he revised his opinion of systematic synonymisation, but did not choose to return them back to species rank. He reduced the different Cupressus species to varietal rank, four as Cupressus arizonica Greene varieties, two as Cupressus goveniana varieties, one as a variety of Cupressus guadalupensis Watson, and finally admitting Cupressus sargentii as a valid species. Despite Wolf, and arguing about the fact that this author gave hint that these new combinations could be acceptable, he justified his choice almost exclusively by very broad morphological considerations. -
Santa Ana Mountains Tecate Cypress (Cupressus Forbesii) Management Plan
Final Santa Ana Mountains Tecate Cypress (Cupressus forbesii) Management Plan Prepared by: Susana Rodriguez-Buritica & Katharine Suding University of California, Berkeley Department of Environmental Sciences, Policy, and Management Berkeley, CA 94720 & Kristine Preston Nature Reserve of Orange County 15600 Sand Canyon Avenue Irvine, CA 92618 Prepared for: California Department of Fish and Game 4949 Viewridge Avenue San Diego, CA 92123 Contract # P0750005 01 & Nature Reserve of Orange County May 17, 2010 Santa Ana Mountains Tecate Cypress Management Plan EXECUTIVE SUMMARY Orange County’s Central and Coastal Natural Community Conservation Plan/Habitat Conservation Plan (NCCP/HCP) was established in 1996 to conserve sensitive plant and animal species on approximately 37,000 acres. Tecate cypress (Cupressus forbesii) is a rare endemic species restricted to several locations in southern California and northern Baja California. The northern most population of Tecate cypress occurs in the Santa Ana Mountains within the NCCP/HCP Central Reserve and receives regulatory coverage under the Plan. This population is threatened by too frequent wildfire. The Nature Reserve of Orange County (NROC) oversees monitoring and management of species within the NCCP/HCP and formed the Tecate Cypress Management Committee (TCMC) to develop a management plan for this species. The committee is composed of land owners, land managers and regulatory agencies with an interest in conserving Tecate cypress in the NCCP/HCP. This management plan was developed by NROC based upon the work of researchers from UC Berkeley and input from the TCMC. The objectives of this management plan included determining the current distribution and demographic structure of the Santa Ana Mountains Tecate cypress population and using this data in ecological models to assess threats to persistence and to identify restoration sites for enhancing the population.