Biodiversity Action Plan for the Tristan Da Cunha Islands
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Conservation Problems on Tristan Da Cunha Byj
28 Oryx Conservation Problems on Tristan da Cunha ByJ. H. Flint The author spent two years, 1963-65, as schoolmaster on Tristan da Cunha, during which he spent four weeks on Nightingale Island. On the main island he found that bird stocks were being depleted and the islanders taking too many eggs and young; on Nightingale, however, where there are over two million pairs of great shearwaters, the harvest of these birds could be greater. Inaccessible Island, which like Nightingale, is without cats, dogs or rats, should be declared a wildlife sanctuary. Tl^HEN the first permanent settlers came to Tristan da Cunha in " the early years of the nineteenth century they found an island rich in bird and sea mammal life. "The mountains are covered with Albatross Mellahs Petrels Seahens, etc.," wrote Jonathan Lambert in 1811, and Midshipman Greene, who stayed on the island in 1816, recorded in his diary "Sea Elephants herding together in immense numbers." Today the picture is greatly changed. A century and a half of human habitation has drastically reduced the larger, edible species, and the accidental introduction of rats from a shipwreck in 1882 accelerated the birds' decline on the main island. Wood-cutting, grazing by domestic stock and, more recently, fumes from the volcano have destroyed much of the natural vegetation near the settlement, and two bird subspecies, a bunting and a flightless moorhen, have become extinct on the main island. Curiously, one is liable to see more birds on the day of arrival than in several weeks ashore. When I first saw Tristan from the decks of M.V. -
Atlantic Ocean
Appendix B – Region 18 Country and regional profiles of volcanic hazard and risk: Atlantic Ocean S.K. Brown1, R.S.J. Sparks1, K. Mee2, C. Vye-Brown2, E.Ilyinskaya2, S.F. Jenkins1, S.C. Loughlin2* 1University of Bristol, UK; 2British Geological Survey, UK, * Full contributor list available in Appendix B Full Download This download comprises the profiles for Region 18: Atlantic Ocean only. For the full report and all regions see Appendix B Full Download. Page numbers reflect position in the full report. The following countries are profiled here: Region 18 Atlantic Ocean Pg.743 Brazil 750 Cape Verde 754 Portugal – Azores 761 Spain – Canary Islands 767 UK – Tristan da Cunha, Nightingale Island, Ascension 775 Brown, S.K., Sparks, R.S.J., Mee, K., Vye-Brown, C., Ilyinskaya, E., Jenkins, S.F., and Loughlin, S.C. (2015) Country and regional profiles of volcanic hazard and risk. In: S.C. Loughlin, R.S.J. Sparks, S.K. Brown, S.F. Jenkins & C. Vye-Brown (eds) Global Volcanic Hazards and Risk, Cambridge: Cambridge University Press. This profile and the data therein should not be used in place of focussed assessments and information provided by local monitoring and research institutions. Region 18: Atlantic Ocean Figure 18.1 The distribution of Holocene volcanoes through the Atlantic Ocean region. The capital cities of the constituent countries are shown. The host countries are identified on the right. Description Region 18: the Atlantic Ocean comprises volcanoes throughout the Atlantic, from an unnamed seamount in the north to the Norwegian territory of Bouvet in the south. Six countries are represented here. -
Types of American Grasses
z LIBRARY OF Si AS-HITCHCOCK AND AGNES'CHASE 4: SMITHSONIAN INSTITUTION UNITED STATES NATIONAL MUSEUM oL TiiC. CONTRIBUTIONS FROM THE United States National Herbarium Volume XII, Part 3 TXE&3 OF AMERICAN GRASSES . / A STUDY OF THE AMERICAN SPECIES OF GRASSES DESCRIBED BY LINNAEUS, GRONOVIUS, SLOANE, SWARTZ, AND MICHAUX By A. S. HITCHCOCK z rit erV ^-C?^ 1 " WASHINGTON GOVERNMENT PRINTING OFFICE 1908 BULLETIN OF THE UNITED STATES NATIONAL MUSEUM Issued June 18, 1908 ii PREFACE The accompanying paper, by Prof. A. S. Hitchcock, Systematic Agrostologist of the United States Department of Agriculture, u entitled Types of American grasses: a study of the American species of grasses described by Linnaeus, Gronovius, Sloane, Swartz, and Michaux," is an important contribution to our knowledge of American grasses. It is regarded as of fundamental importance in the critical sys- tematic investigation of any group of plants that the identity of the species described by earlier authors be determined with certainty. Often this identification can be made only by examining the type specimen, the original description being inconclusive. Under the American code of botanical nomenclature, which has been followed by the author of this paper, "the nomenclatorial t}rpe of a species or subspecies is the specimen to which the describer originally applied the name in publication." The procedure indicated by the American code, namely, to appeal to the type specimen when the original description is insufficient to identify the species, has been much misunderstood by European botanists. It has been taken to mean, in the case of the Linnsean herbarium, for example, that a specimen in that herbarium bearing the same name as a species described by Linnaeus in his Species Plantarum must be taken as the type of that species regardless of all other considerations. -
Red-Footed Booby Helper at Great Frigatebird Nests
264 SHORT COMMUNICATIONS NECTS MEANS ECTS MEANS ICATE SAMPLE SIZE S.D. SAMPLE SIZE 70 IN DAYS FIGURE 2. Culmen length against age of Brown FIGURE 1. Weight against age of Brown Noddy Noddy chicks on Manana Island, Hawaii in 1972. chicks on Manana Island, Hawaii in 1972. about the thirty-fifth day; apparently Brown Noddies on Christmas Island grow more rapidly than those on 5.26 g/day (SD = 1.18 g/day), and chick growth rate Manana. More data are required for a refined analysis and fledging age were negatively correlated (r = of intraspecific variation in growth rates of Brown -0.490, N = 19, P < 0.05). Noddy young. Seventeen of the chicks were weighed both at the This paper is based upon my doctoral dissertation age of fledging and from 3 to 12 days later; there was submitted to the University of Hawaii. I thank An- no significant recession in weight after fledging (t = drew J. Berger for guidance and criticism. The 1.17, P > 0.2), as suggested for certain terns (e.g., Hawaii State Division of Fish and Game kindly LeCroy and LeCroy 1974, Bird-Banding 45:326). granted me permission to work on Manana. This Dorward and Ashmole (1963, Ibis 103b: 447) mea- study was supported by the Department of Zoology sured growth in weight and culmen length of Brown of the University of Hawaii, by an NSF Graduate Noddies on Ascension Island in the Atlantic; scatter Fellowship, and by a Mount Holyoke College Faculty diagrams of their data indicate growth functions very Grant. -
Plant Fact Sheet for Annual Hairgrass (Deschampsia Danthonioides)
Plant Fact Sheet ANNUAL HAIRGRASS Status Please consult the PLANTS Web site and your State Deschampsia danthonioides Department of Natural Resources for this plant’s current (Trin.) Munro status (e.g. threatened or endangered species, state Plant Symbol = DEDA noxious status, and wetland indicator values). Contributed by: USDA NRCS Plant Materials Center, Description and Adaptation Annual hairgrass is a fine textured, native, cool season Corvallis, Oregon grass with smooth, slender stems (culms) that are 10 to 60 cm tall. The form is upright to spreading, short, and somewhat tufted. The narrow leaf blades are hairless, rough on the edges, slightly in-rolled, 0.5 to 1.5 (2) mm wide, and 1 to 10 cm long. Flower heads (panicles) are open, 7 to 25 cm long, with ascending lower branches. Annual hairgrass occurs from near sea level at the coast to 8,000 feet in the Rocky Mountains. It is primarily found from Alaska south to Baja California and east to Montana and New Mexico; also the Northeast US and Chile. Key to identification: Annual hairgrass can be distinguished from slender hairgrass (Deschampsia elongata) and tufted hairgrass (Deschampsia cespitosa) by its weaker root development, fewer leaves, and smaller stature. Without close inspection it may be confused with other annual grasses, such as annual fescues (Vulpia spp.). Both may occur in waste areas. Consult botanical keys for proper identification. Relative abundance in wild: While most common in the Photo by Dale Darris, USDA NRCS Corvallis PMC. Pacific Coast states, the species can still be hard to locate. However, it can occur in large stands, especially in vernal Alternative Names pools dominated by annuals. -
Some Biological Observations on Pale Fruit, a Viroid-Incited Disease of Cucumber
Neth.J . PI.Path . 80(1974 )85-9 6 Some biological observations on pale fruit, a viroid-incited disease of cucumber H. J. M. VAN DORST1 and D. PETERS2 1 Glasshouse CropsResearc han d Experiment Station, Naaldwijlk 2 Laboratory ofVirology ,Agricultura l University, Wageningen Accepted 13 December 1973 Abstract A viroid-incited disease characterized by palefruits , crumpledflowers, an d rugosity and chlorosis on the leaves of cucumber, occurs occasionally in cucumber crops grown in glasshouses in the Nether lands. The disease is found primarily in crops planted in spring, rarely in those planted in summer but not in those planted in late summer. The pathogen can be transmitted with sap, during pruning, bygraftin g and with dodder to cucumber and a number of other cucurbitaceous species,but not with M. persicae.Ther e is no evidence for seed or nematode transmission. The incubation period js 21 daysa thig htemperature s(3 0°C )bu tshorte r after inoculationb yrazorblad eslashing . The number of glasshouses with the disease has increased since 1965,bu t the number of diseased plants is usually low. The initial distribution of diseased plants in the glasshouses suggests that the pathogeni sintroduce db ya ninsect . Introduction In 1963a disease in cucumber especially attracting attention by a light green colour on the fruits, but also with affectedflowers an d young leaves, occurred in two glass houses in the western part of the Netherlands. The disease, now calledpal efrui t dis ease,ha ssinc ebee n observed indifferen t places overth ewhol e country. The number ofaffecte d plantsi na glasshous ei smostl yles stha n0. -
Seabird Year-Round and Historical Feeding Ecology: Blood and Feather Δ13c and Δ15n Values Document Foraging Plasticity of Small Sympatric Petrels
Vol. 505: 267–280, 2014 MARINE ECOLOGY PROGRESS SERIES Published May 28 doi: 10.3354/meps10795 Mar Ecol Prog Ser FREEREE ACCESSCCESS Seabird year-round and historical feeding ecology: blood and feather δ13C and δ15N values document foraging plasticity of small sympatric petrels Yves Cherel1,*, Maëlle Connan1, Audrey Jaeger1, Pierre Richard2 1Centre d’Etudes Biologiques de Chizé, UMR 7372 du CNRS et de l’Université de La Rochelle, BP 14, 79360 Villiers-en-Bois, France 2Laboratoire Littoral, Environnement et Sociétés, UMR 7266 du CNRS et de l’Université de La Rochelle, 2 rue Olympe de Gouges, 17000 La Rochelle, France ABSTRACT: The foraging ecology of small seabirds remains poorly understood because of the dif- ficulty of studying them at sea. Here, the extent to which 3 sympatric seabirds (blue petrel, thin- billed prion and common diving petrel) alter their foraging ecology across the annual cycle was investigated using stable isotopes. δ13C and δ15N values were used as proxies of the birds’ foraging habitat and diet, respectively, and were measured in 3 tissues (plasma, blood cells and feathers) that record trophic information at different time scales. Long-term temporal changes were inves- tigated by measuring feather isotopic values from museum specimens. The study was conducted at the subantarctic Kerguelen Islands and emphasizes 4 main features. (1) The 3 species highlight a strong connection between subantarctic and Antarctic pelagic ecosystems, because they all for- aged in Antarctic waters at some stages of the annual cycle. (2) Foraging niches are stage- dependent, with petrels shifting their feeding grounds during reproduction either from oceanic to productive coastal waters (common diving petrel) or from subantarctic to high-Antarctic waters where they fed primarily on crustaceans (blue petrel and thin-billed prion). -
S41467-020-18361-4.Pdf
ARTICLE https://doi.org/10.1038/s41467-020-18361-4 OPEN Seafloor evidence for pre-shield volcanism above the Tristan da Cunha mantle plume ✉ Wolfram H. Geissler 1 , Paul Wintersteller 2,3, Marcia Maia4, Anne Strack3, Janina Kammann5, Graeme Eagles 1, Marion Jegen6, Antje Schloemer1,7 & Wilfried Jokat 1,2 Tristan da Cunha is assumed to be the youngest subaerial expression of the Walvis Ridge hot spot. Based on new hydroacoustic data, we propose that the most recent hot spot volcanic 1234567890():,; activity occurs west of the island. We surveyed relatively young intraplate volcanic fields and scattered, probably monogenetic, submarine volcanoes with multibeam echosounders and sub-bottom profilers. Structural and zonal GIS analysis of bathymetric and backscatter results, based on habitat mapping algorithms to discriminate seafloor features, revealed numerous previously-unknown volcanic structures. South of Tristan da Cunha, we discovered two large seamounts. One of them, Isolde Seamount, is most likely the source of a 2004 submarine eruption known from a pumice stranding event and seismological analysis. An oceanic core complex, identified at the intersection of the Tristan da Cunha Transform and Fracture Zone System with the Mid-Atlantic Ridge, might indicate reduced magma supply and, therefore, weak plume-ridge interaction at present times. 1 Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Am Alten Hafen 26, 27568 Bremerhaven, Germany. 2 Faculty of Geosciences, University of Bremen, Klagenfurter Str. 4, 28359 Bremen, Germany. 3 MARUM—Center of Marine Environmental Sciences, University of Bremen, Leobener Str. 8, 28359 Bremen, Germany. 4 CNRS-UBO Laboratoire Domaines Océaniques, Institut Universitaire Européen de la Mer, 29280 Plouzané, France. -
Island Biology Island Biology
IIssllaanndd bbiioollooggyy Allan Sørensen Allan Timmermann, Ana Maria Martín González Camilla Hansen Camille Kruch Dorte Jensen Eva Grøndahl, Franziska Petra Popko, Grete Fogtmann Jensen, Gudny Asgeirsdottir, Hubertus Heinicke, Jan Nikkelborg, Janne Thirstrup, Karin T. Clausen, Karina Mikkelsen, Katrine Meisner, Kent Olsen, Kristina Boros, Linn Kathrin Øverland, Lucía de la Guardia, Marie S. Hoelgaard, Melissa Wetter Mikkel Sørensen, Morten Ravn Knudsen, Pedro Finamore, Petr Klimes, Rasmus Højer Jensen, Tenna Boye Tine Biedenweg AARHUS UNIVERSITY 2005/ESSAYS IN EVOLUTIONARY ECOLOGY Teachers: Bodil K. Ehlers, Tanja Ingversen, Dave Parker, MIchael Warrer Larsen, Yoko L. Dupont & Jens M. Olesen 1 C o n t e n t s Atlantic Ocean Islands Faroe Islands Kent Olsen 4 Shetland Islands Janne Thirstrup 10 Svalbard Linn Kathrin Øverland 14 Greenland Eva Grøndahl 18 Azores Tenna Boye 22 St. Helena Pedro Finamore 25 Falkland Islands Kristina Boros 29 Cape Verde Islands Allan Sørensen 32 Tristan da Cunha Rasmus Højer Jensen 36 Mediterranean Islands Corsica Camille Kruch 39 Cyprus Tine Biedenweg 42 Indian Ocean Islands Socotra Mikkel Sørensen 47 Zanzibar Karina Mikkelsen 50 Maldives Allan Timmermann 54 Krakatau Camilla Hansen 57 Bali and Lombok Grete Fogtmann Jensen 61 Pacific Islands New Guinea Lucía de la Guardia 66 2 Solomon Islands Karin T. Clausen 70 New Caledonia Franziska Petra Popko 74 Samoa Morten Ravn Knudsen 77 Tasmania Jan Nikkelborg 81 Fiji Melissa Wetter 84 New Zealand Marie S. Hoelgaard 87 Pitcairn Katrine Meisner 91 Juan Fernandéz Islands Gudny Asgeirsdottir 95 Hawaiian Islands Petr Klimes 97 Galápagos Islands Dorthe Jensen 102 Caribbean Islands Cuba Hubertus Heinicke 107 Dominica Ana Maria Martin Gonzalez 110 Essay localities 3 The Faroe Islands Kent Olsen Introduction The Faroe Islands is a treeless archipelago situated in the heart of the warm North Atlantic Current on the Wyville Thompson Ridge between 61°20’ and 62°24’ N and between 6°15’ and 7°41’ W. -
Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee
Biodiversity: the UK Overseas Territories Compiled by S. Oldfield Edited by D. Procter and L.V. Fleming ISBN: 1 86107 502 2 © Copyright Joint Nature Conservation Committee 1999 Illustrations and layout by Barry Larking Cover design Tracey Weeks Printed by CLE Citation. Procter, D., & Fleming, L.V., eds. 1999. Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee. Disclaimer: reference to legislation and convention texts in this document are correct to the best of our knowledge but must not be taken to infer definitive legal obligation. Cover photographs Front cover: Top right: Southern rockhopper penguin Eudyptes chrysocome chrysocome (Richard White/JNCC). The world’s largest concentrations of southern rockhopper penguin are found on the Falkland Islands. Centre left: Down Rope, Pitcairn Island, South Pacific (Deborah Procter/JNCC). The introduced rat population of Pitcairn Island has successfully been eradicated in a programme funded by the UK Government. Centre right: Male Anegada rock iguana Cyclura pinguis (Glen Gerber/FFI). The Anegada rock iguana has been the subject of a successful breeding and re-introduction programme funded by FCO and FFI in collaboration with the National Parks Trust of the British Virgin Islands. Back cover: Black-browed albatross Diomedea melanophris (Richard White/JNCC). Of the global breeding population of black-browed albatross, 80 % is found on the Falkland Islands and 10% on South Georgia. Background image on front and back cover: Shoal of fish (Charles Sheppard/Warwick -
Illinois Exotic Species List
Exotic Species in Illinois Descriptions for these exotic species in Illinois will be added to the Web page as time allows for their development. A name followed by an asterisk (*) indicates that a description for that species can currently be found on the Web site. This list does not currently name all of the exotic species in the state, but it does show many of them. It will be updated regularly with additional information. Microbes viral hemorrhagic septicemia Novirhabdovirus sp. West Nile virus Flavivirus sp. Zika virus Flavivirus sp. Fungi oak wilt Ceratocystis fagacearum chestnut blight Cryphonectria parasitica Dutch elm disease Ophiostoma novo-ulmi and Ophiostoma ulmi late blight Phytophthora infestans white-nose syndrome Pseudogymnoascus destructans butternut canker Sirococcus clavigignenti-juglandacearum Plants okra Abelmoschus esculentus velvet-leaf Abutilon theophrastii Amur maple* Acer ginnala Norway maple Acer platanoides sycamore maple Acer pseudoplatanus common yarrow* Achillea millefolium Japanese chaff flower Achyranthes japonica Russian knapweed Acroptilon repens climbing fumitory Adlumia fungosa jointed goat grass Aegilops cylindrica goutweed Aegopodium podagraria horse chestnut Aesculus hippocastanum fool’s parsley Aethusa cynapium crested wheat grass Agropyron cristatum wheat grass Agropyron desertorum corn cockle Agrostemma githago Rhode Island bent grass Agrostis capillaris tree-of-heaven* Ailanthus altissima slender hairgrass Aira caryophyllaea Geneva bugleweed Ajuga genevensis carpet bugleweed* Ajuga reptans mimosa -
Species List
Antarctica Trip Report November 30 – December 18, 2017 | Compiled by Greg Smith With Greg Smith, guide, and participants Anne, Karen, Anita, Alberto, Dick, Patty & Andy, and Judy & Jerry Bird List — 78 Species Seen Anatidae: Ducks, Geese, and Swans (8) Upland Goose (Chloephaga picta) Only seen on the Falklands, and most had young or were on nests. Kelp Goose (Chloephaga hybrid) On the beach (or close to the beach) at West Point and Carcass Islands. Ruddy-headed Goose (Chloephaga rubidiceps) Mixed in with the grazing Upland Geese on the Falklands. Flightless Steamer Duck (Tachyeres pteneres) Found on both islands that we visited, and on Stanley. Crested Duck (Lophonetta specularioides) Not common at all with only a few seen in a pond on Carcass Island. Yellow-billed (Speckled) Teal (Anas flavirostris) Two small flocks were using freshwater ponds. Yellow-billed Pintail (Anas georgica) Fairly common on South Georgia. South Georgia Pintail (Anas georgica georgica) Only on South Georgia and seen on every beach access. Spheniscidae: Penguins (7) King Penguin (Aptenodytes patagonicus) Only on South Georgia and there were thousands and thousands. Gentoo Penguin (Pygoscelis papua) Not as many as the Kings, but still thousands. Magellanic Penguin (Spheniscus magellanicus) Only on the Falklands and not nearly as common as the Gentoo. Macaroni Penguin (Eudyptes chrysolophus) Saw a colony at Elsihul Bay on South Georgia. Southern Rockhopper Penguin (Eudyptes chrysocome) A nesting colony among the Black-browed Albatross on West Point Island. Adelie Penguin (Pygoscelis adeliae) Landed near a colony of over 100,000 pairs at Paulet Island on the Peninsula. Chinstrap Penguin (Pygoscelis antarcticus) Seen on the Peninsula and we watched a particularly intense Leopard Seal hunt and kill a Chinstrap.