Soil Erosion Model for Tristan Da Cunha
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Phylogenetic Relationships in the Order Ericales S.L.: Analyses of Molecular Data from Five Genes from the Plastid and Mitochondrial Genomes1
American Journal of Botany 89(4): 677±687. 2002. PHYLOGENETIC RELATIONSHIPS IN THE ORDER ERICALES S.L.: ANALYSES OF MOLECULAR DATA FROM FIVE GENES FROM THE PLASTID AND MITOCHONDRIAL GENOMES1 ARNE A. ANDERBERG,2,5 CATARINA RYDIN,3 AND MARI KAÈ LLERSJOÈ 4 2Department of Phanerogamic Botany, Swedish Museum of Natural History, P.O. Box 50007, SE-104 05 Stockholm, Sweden; 3Department of Systematic Botany, University of Stockholm, SE-106 91 Stockholm, Sweden; and 4Laboratory for Molecular Systematics, Swedish Museum of Natural History, P.O. Box 50007, SE-104 05 Stockholm, Sweden Phylogenetic interrelationships in the enlarged order Ericales were investigated by jackknife analysis of a combination of DNA sequences from the plastid genes rbcL, ndhF, atpB, and the mitochondrial genes atp1 and matR. Several well-supported groups were identi®ed, but neither a combination of all gene sequences nor any one alone fully resolved the relationships between all major clades in Ericales. All investigated families except Theaceae were found to be monophyletic. Four families, Marcgraviaceae, Balsaminaceae, Pellicieraceae, and Tetrameristaceae form a monophyletic group that is the sister of the remaining families. On the next higher level, Fouquieriaceae and Polemoniaceae form a clade that is sister to the majority of families that form a group with eight supported clades between which the interrelationships are unresolved: Theaceae-Ternstroemioideae with Ficalhoa, Sladenia, and Pentaphylacaceae; Theaceae-Theoideae; Ebenaceae and Lissocarpaceae; Symplocaceae; Maesaceae, Theophrastaceae, Primulaceae, and Myrsinaceae; Styr- acaceae and Diapensiaceae; Lecythidaceae and Sapotaceae; Actinidiaceae, Roridulaceae, Sarraceniaceae, Clethraceae, Cyrillaceae, and Ericaceae. Key words: atpB; atp1; cladistics; DNA; Ericales; jackknife; matR; ndhF; phylogeny; rbcL. Understanding of phylogenetic relationships among angio- was available for them at the time, viz. -
Invasions but Not Extinctions Change Phylogenetic Diversity of Angiosperm Assemblage on Southeastern Pacific Oceanic Islands
RESEARCH ARTICLE Invasions but not extinctions change phylogenetic diversity of angiosperm assemblage on southeastern Pacific Oceanic islands Gasto n O. Carvallo1☯*, Sergio A. Castro2,3☯ 1 Instituto de BiologõÂa, Facultad de Ciencias, Pontificia Universidad CatoÂlica de ValparaõÂso, ValparaõÂso, Chile, 2 Laboratorio de EcologõÂa y Biodiversidad, Facultad de QuõÂmica y BiologõÂa, Universidad de Santiago, Santiago, Chile, 3 Centro para el Desarrollo de la Nanociencia y NanotecnologõÂa (CEDENNA), Santiago, a1111111111 Chile a1111111111 a1111111111 ☯ These authors contributed equally to this work. a1111111111 * [email protected] a1111111111 Abstract We assessed changes in phylogenetic diversity of angiosperm flora on six oceanic islands OPEN ACCESS located in the southeastern Pacific Ocean, by comparing flora from two periods: the pre- Citation: Carvallo GO, Castro SA (2017) Invasions European colonization of islands and current times. We hypothesize that, in the time but not extinctions change phylogenetic diversity of between these periods, extinction of local plant species and addition of exotic plants modi- angiosperm assemblage on southeastern Pacific Oceanic islands. PLoS ONE 12(8): e0182105. fied phylogenetic-α-diversity at different levels (deeper and terminal phylogeny) and https://doi.org/10.1371/journal.pone.0182105 increased phylo-β-diversity among islands. Based on floristic studies, we assembled a phy- Editor: Ulrich Melcher, Oklahoma State University, logenetic tree from occurrence data that includes 921 species, of which 165 and 756 were UNITED STATES native or exotic in origin, respectively. Then, we studied change in the phylo-α-diversity and Received: March 3, 2017 phylo-β-diversity (1 ±Phylosor) by comparing pre-European and current times. Despite extinction of 18 native angiosperm species, an increase in species richness and phylo- - Accepted: July 12, 2017 α diversity was observed for all islands studied, attributed to introduction of exotic plants Published: August 1, 2017 (between 6 to 477 species per island). -
Falkland Island Peatland Development Processes and the Pervasive
Manuscript File 1 Falkland Island peatland development 2 processes and the pervasive presence of 3 fire 4 5 Dmitri Mauquoy1#, Richard J Payne2*, Kirill V. Babeshko3, Rebecca Bartlett4, Ian 6 Boomer4, Hannah Bowey1, Chris D. Evans5, Fin Ring-Hrubesh2, David Muirhead1, 7 Matthew O’Callaghan4, Natalia Piotrowska6, Graham Rush2, Thomas Sloan2, Craig 8 Smeaton7, Andrey N. Tsyganov8,9, Yuri A. Mazei8,9 9 10 1. Geography and Environment, School of Geosciences, University of 11 Aberdeen, St Mary’s Building, Aberdeen AB24 3UF, United Kingdom 12 2. Environment and Geography, University of York, York YO10 5NG, United 13 Kingdom 14 3. Department of Zoology and Ecology, Penza State University, 440026, Penza, 15 Russia 16 4. School of Geography, Earth and Environmental Sciences, University of 17 Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom 18 5. Centre for Ecology & Hydrology, Environment Centre Wales, Deiniol Road, 19 Bangor, Gwynedd LL57 2UW, United Kingdom 20 6. Silesian University of Technology, Institute of Physics-CSE, Gliwice, Poland. 21 7. School of Geography & Sustainable Development, University of St Andrews, 22 St Andrews, KY16 9AL, UK 23 8. Department of General Ecology and Hydrobiology, Lomonosov Moscow State 24 University, 119991, Moscow, Russia 25 9. A.N. Severtsov Institute of Ecology and Evolution RAS, 119071, Moscow, 26 Russia 1 27 #Corresponding author, [email protected] 28 *Deceased 29 30 Abstract 31 32 Palaeoecological analyses of Falkland Island peat profiles have largely been 33 confined to pollen analyses. In order to improve understanding of long-term Falkland 34 Island peat development processes, the plant macrofossil and stable isotope 35 stratigraphy of an 11,550 year Falkland Island Cortaderia pilosa (‘whitegrass’) peat 36 profile was investigated. -
Batatasin-III and the Allelopathic Capacity of Empetrum Nigrum
Nordic Journal of Botany 33: 225–231, 2015 doi: 10.1111/njb.00559, ISSN 1756-1051 © 2014 Th e Authors. Nordic Journal of Botany © 2014 Nordic Society Oikos Subject Editor: Per Milberg. Editor-in-Chief: Torbjörn Tyler. Accepted 4 June 2014 Batatasin-III and the allelopathic capacity of Empetrum nigrum Victoria T. Gonz á lez , Olavi Junttila , Bente Lindg å rd , Rigmor Reiersen , Kajetan Trost and Kari Anne Br å then V. T. Gonz á lez ([email protected]), O. Junttila, B. Lindg å rd, R. Reiersen and A. Br å then, Dept of Arctic and Marine Biology, Univ. of Troms ø , NO-9037 Troms ø , Norway. VTG also at: Bioforsk Jord og Milj ø Svanhovd, 9925 Svanvik, Norway. – K. Trost, Wine Research Centre, Univ. of Nova Gorica, Vipavska cesta 11c, 5270 Ajdovscina, Slovenia. Batatasin-III (3,3-dihydroxy-5-methoxybibenzyl) is a phenolic compound associated with the allelopathic eff ect of the evergreen dwarf shrub Empetrum nigrum , and has been referred to as the causal factor for the species being successful in dominating extensive ecosystems. Yet, only a few plant species have been tested for their response to batatasin-III, and little is known about whether environmental factors modify this allelopathic eff ect. In this study, we tested the inhibitory eff ect of purifi ed batatasin-III through bioassays on 24 vascular plant species and, for certain species, we tested if this eff ect depended on growth substrate (mineral vs organic substrate), pH, and fertilization. Moreover, we tested if batatasin-III predicted the allelopathic eff ect of E. -
The Natural History of Tristan Da Cunha
The Natural History of Tristan da Cunha Paul Tyler and Alison Rothwell The Natural History of Tristan da Cunha Contents Page 1 Habitats Page 12 Birds Page 28 Marine Life Page 40 Landscape Paul Tyler and Alison Rothwell The Natural History of Tristan da Cunha 1 Habitats What is a habitat? What are the main habitats on A habitat describes the kind of place where Tristan? animals and plants live. The main habitats found on land on the main island There are different habitats in Tristan where you of Tristan are described in the following pages. They will find different kinds of animals and plants are mainly recognised by the kinds of plants that living. For instance at the patches you will find grow there. lots of farm grass, whereas up on the base there will be lots of bog ferns growing - these plants are different because they live under different conditions. What makes them different? Altitude - some plants can stand the cold better than others - the higher you go the colder it gets What makes habitats the way they are? Moisture - some plants do better in wet conditions than others The reason one habitat is different to another can depend on a number of things. For example, Shelter - Some plants such as trees prefer places some plants need shelter, some can’t survive where it’s not too windy being frozen, and some prefer very wet soil. So the plants that grow in a particular place Rock and soil type - some plants can live on bare will be those that are best able to survive the rock but most need some kind of soil conditions found there. -
Black Crowberry (Empetrum Nigrum) L
Conservation Assessment for Black crowberry (Empetrum nigrum) L. USDA Forest Service, Eastern Region March 2002 Hiawatha National Forest This document is undergoing peer review, comments welcome CONSERVATION ASSESSMENT FOR BLACK CROWBERRY (EMPETRUM NIGRUM) L. 1 This Conservation Assessment was prepared to compile the published and unpublished information on the subject taxon or community; or this document was prepared by another organization and provides information to serve as a Conservation Assessment for the Eastern Region of the Forest Service. It does not represent a management decision by the U.S. Forest Service. Though the best scientific information available was used and subject experts were consulted in preparation of this document, it is expected that new information will arise. In the spirit of continuous learning and adaptive management, if you have information that will assist in conserving the subject taxon, please contact the Eastern Region of the Forest Service - Threatened and Endangered Species Program at 310 Wisconsin Avenue, Suite 580 Milwaukee, Wisconsin 53203. CONSERVATION ASSESSMENT FOR BLACK CROWBERRY (EMPETRUM NIGRUM) L. 1 Table of contents ACKNOWLEDGEMENTS ......................................................................... 3 EXECUTIVE SUMMARY .......................................................................... 4 NOMENCLATURE AND TAXONOMY .................................................. 4 DESCRIPTION OF SPECIES .................................................................... 5 HABITAT TYPES -
Native and Exotic Plants with Edible Fleshy Fruits Utilized in Patagonia and Their Role As Sources of Local Functional Foods Melina Fernanda Chamorro and Ana Ladio*
Chamorro and Ladio BMC Complementary Medicine and Therapies (2020) 20:155 BMC Complementary https://doi.org/10.1186/s12906-020-02952-1 Medicine and Therapies RESEARCH ARTICLE Open Access Native and exotic plants with edible fleshy fruits utilized in Patagonia and their role as sources of local functional foods Melina Fernanda Chamorro and Ana Ladio* Abstract Background: Traditionally part of the human diet, plants with edible fleshy fruits (PEFF) contain bioactive components that may exert physiological effects beyond nutrition, promoting human health and well-being. Focusing on their food-medicine functionality, different ways of using PEFF were studied in a cross-sectional way using two approaches: a bibliographical survey and an ethnobotanical case study in a rural community of Patagonia, Argentina. Methods: A total of 42 studies were selected for the bibliographical review. The case study was carried out with 80% of the families inhabiting the rural community of Cuyín Manzano, using free listing, interviews, and participant observation. In both cases we analyzed species richness and use patterns through the edible consensus and functional consensus indices. Local foods, ailments, medicines and drug plants were also registered. Results: The review identified 73 PEFF, the majority of which (78%) were native species, some with the highest use consensus. PEFF were used in 162 different local foods, but mainly as fresh fruit. Of the total, 42% were used in a functional way, in 54 different medicines. The principal functional native species identified in the review were Aristotelia chilensis and Berberis microphylla. In the case study 20 PEFF were in current use (50% were native), and consensus values were similar for native and exotic species. -
Falkland Islands Species List
Falkland Islands Species List Day Common Name Scientific Name x 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 1 BIRDS* 2 DUCKS, GEESE, & WATERFOWL Anseriformes - Anatidae 3 Black-necked Swan Cygnus melancoryphus 4 Coscoroba Swan Coscoroba coscoroba 5 Upland Goose Chloephaga picta 6 Kelp Goose Chloephaga hybrida 7 Ruddy-headed Goose Chloephaga rubidiceps 8 Flying Steamer-Duck Tachyeres patachonicus 9 Falkland Steamer-Duck Tachyeres brachypterus 10 Crested Duck Lophonetta specularioides 11 Chiloe Wigeon Anas sibilatrix 12 Mallard Anas platyrhynchos 13 Cinnamon Teal Anas cyanoptera 14 Yellow-billed Pintail Anas georgica 15 Silver Teal Anas versicolor 16 Yellow-billed Teal Anas flavirostris 17 GREBES Podicipediformes - Podicipedidae 18 White-tufted Grebe Rollandia rolland 19 Silvery Grebe Podiceps occipitalis 20 PENGUINS Sphenisciformes - Spheniscidae 21 King Penguin Aptenodytes patagonicus 22 Gentoo Penguin Pygoscelis papua Cheesemans' Ecology Safaris Species List Updated: April 2017 Page 1 of 11 Day Common Name Scientific Name x 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 23 Magellanic Penguin Spheniscus magellanicus 24 Macaroni Penguin Eudyptes chrysolophus 25 Southern Rockhopper Penguin Eudyptes chrysocome chrysocome 26 ALBATROSSES Procellariiformes - Diomedeidae 27 Gray-headed Albatross Thalassarche chrysostoma 28 Black-browed Albatross Thalassarche melanophris 29 Royal Albatross (Southern) Diomedea epomophora epomophora 30 Royal Albatross (Northern) Diomedea epomophora sanfordi 31 Wandering Albatross (Snowy) Diomedea exulans exulans 32 Wandering -
(Black Spruce)- Pleurozium Forests of South-Eastern Labrador, Canada Author(S): David R
Vegetation Development Following Fire in Picea Mariana (Black Spruce)- Pleurozium Forests of South-Eastern Labrador, Canada Author(s): David R. Foster Source: Journal of Ecology, Vol. 73, No. 2 (Jul., 1985), pp. 517-534 Published by: British Ecological Society Stable URL: http://www.jstor.org/stable/2260491 . Accessed: 05/08/2011 12:57 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. British Ecological Society is collaborating with JSTOR to digitize, preserve and extend access to Journal of Ecology. http://www.jstor.org Journal of Ecology (1985), 73, 5 17-534 VEGETATION DEVELOPMENT FOLLOWING FIRE IN PICEA MARIANA (BLACK SPRUCE)-PLEUR OZIUM FORESTS OF SOUTH-EASTERN LABRADOR, CANADA DAVID R. FOSTER Harvard University,Harvard Forest, Petersham, Massachusetts 01366, U.S.A. SUMMARY (1) The pattern of post-fire vegetation development in Picea mariana (black spruce)- Pleurozium forests in south-eastern Labrador,Canada, is evaluated using palaeoecological methods and vegetation analysis of extant stands. (2) Macrofossil analysis of mor humus profiles in mature stands yields the following stratigraphy: mineral soil-charcoal-Polytrichum juniperinum-Cladonia lichens- Pleurozium schreberi-feather mosses and Sphagnum girgensohnii. The stratigraphic record of the post-fire dynamics of the vegetation at individual sites strengthens the conclusions obtained from the detailed analysis of a chronosequence of stands. -
Overview of Vegetation Association Classification and Fact Sheets Vegetation Associations Are Part of the Yukon ELC Framework
Overview of Vegetation Association Classification and Fact Sheets Vegetation associations are part of the Yukon ELC Framework. An association is a vegetation classification unit “defined on the basis of a characteristic range of species composition, diagnostic species occurrence, habitat conditions, and physiognomy”. They describe the current vegetation of Yukon and are specifically used to characterize the vegetation growing on a specific ecosite. However, they can also be used separately to describe vegetation (i.e., without the ecosite classification). Canadian National Vegetation Classification, or CNVC (http://cnvc-cnvc.ca) system protocols are used to identify, name and describe vegetation associations and subassociations. The Yukon vegetation associations are sometimes at a different scale than the national associations. For example, a Yukon association is sometimes a national subassociation. This is a result of the process of development of national associations where existing vegetation types were correlated between jurisdictions so jurisdictional protocols sometimes had to be taken into account. Names and Codes Every vegetation association has a name and code. The names and codes are described briefly here— see Yukon Ecological and Landscape Classification and Mapping Guidelines for more detail. Vegetation associations are named according to one or more dominant and/or indicator species. Species of different “layers” — i.e., tree, shrub, herb or moss/lichen — are separated by a forward slash (/). Species within the same layer are separated by an en dash (–). Vegetation subassociations are generally used to characterize variation in species composition that is not considered significant enough to be an association. A single species name is appended to the association to name the subassociation. -
Parque Nacional Tierra Del Fuego Flora
Parque Nacional Tierra del Fuego Flora • Common English Name (Nombre Español o Local)Order Family Genus species) Monocotyledons (Monocotyledones) • Arrowgrass, Marsh (??) (Najadales Juncaginaceae Triglochin palustris) • Arrowgrass, Seaside (??) (Najadales Juncaginaceae Triglochin maritima) • Bentgrass, Common (Pasto Quila) (Poales Gramineae/Poaceae Agrostis capillaris) • Bentgrass, Upland (??) (Poales Gramineae/Poaceae Agrostis perennans) • Bluegrass (??) (Poales Gramineae/Poaceae Poa alopecurus) • Bluegrass (??) (Poales Gramineae/Poaceae Poa breviculmis) • Bluegrass (??) (Poales Gramineae/Poaceae Poa rigidifolia) • Bluegrass (??) (Poales Gramineae/Poaceae Poa scaberula) • Bluegrass (Möra-Shúka) (Poales Gramineae/Poaceae Poa yaganica) • Bluegrass, Annual (Pastito de Invierno) (Poales Gramineae/Poaceae Poa annua) • Bluegrass, Canada (??) (Poales Gramineae/Poaceae Poa compressa) • Bluegrass, Kentucky (Pasto de Mallin) (Poales Gramineae/Poaceae Poa pratensis) • Bluegrass, Northern (??) (Poales Gramineae/Poaceae Poa stenantha) • Bulrush, California (Junco) (Cyperales Cyperaceae Schoenoplectus californicus) • Bulrush, Nevada (Scirpus) (Cyperales Cyperaceae Amphiscirpus nevadensis) • Foxtail, Meadow (Alopecuro de los Prados-cola de Zorro) (Poales Gramineae/Poaceae Alopecurus pratensis) • Grass, Black (??) (Poales Gramineae/Poaceae Alopecurus magellanicus) • Grass, Fiber Optic (??) (Cyperales Cyperaceae Isolepis cernua) • Grass, Small Tussock (??) (Poales Gramineae/Poaceae Festuca magellanica) • Grass, Sweet Holy (Ratonera) (Poales Gramineae/Poaceae -
Pollination Issues with Three Northern Berry Plants for Newfoundland & Labrador
Pollination Issues with Three Northern Berry Plants for Newfoundland & Labrador Prepared by Peter G. Kevan Scientific Director, NSERC-CANPOLIN June, 2009 Crowberry or Blackberry; Empetrum nigrum L. (Empetraceae) This species is described as dioecious, with the majority of flowers being male. The sex ratio of the plants is not known. The male plant’s pink flowers have three stamens and the vestige of a pistil. The female plant’s purple flowers have a short style with a black, shiny stigma with six to nine lobes (rays) about 2mm in diameter. The stigmatic exudate may contain sugar. Unisexual flowers are also known to occur. It has been suggested that pollination can be by wind and by insects (flies) but bees (Colletes and Andrena) have also been observed visiting the flowers. Partridgeberry or Lignonberry; Vaccinium vitis-idaea L. (Ericaceae) Sometimes Vaccinium vitis-idea is called crowberry. V. vitis-idea is pollinated in the same way as lowbush blueberry, but possibly with minor differences. Plants in northern Labrador have smaller flowers than those elsewhere to the south, but the situation in southern Labrador needs investigating. The flowers are described as having stigmas and anthers that are sexually functional at the same time (homogamous), or with stigmas that are receptive before the pollen is shed from the anthers (protogynous). Although the pollination mechanism of the larger flowers of southern regions is considered to rely on insects, especially bumblebees, old literature suggests that the smaller flowers can be self-pollinating. In some populations, the flowers of some plants, or the plants themselves, may be functionally male by suppression of the development of the pistil (if this situation describes the functional sex of whole plants, i.e.