CONSERVATION of ARCTIC FLORA and FAUNA (CAFF) FLORA GROUP Acknowledgements I
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The Newfoundland Rare Plant Project Including an Update to the Rare Vascular Plants of the Island of Newfoundland
The Newfoundland Rare Plant Project Including an Update to the Rare Vascular Plants of the Island of Newfoundland April 2004 prepared by: Nathalie Djan-Chékar, Project Manager Newfoundland and Labrador Inland Fish and Wildlife Division and Claudia Hanel, Assistant Botanist Atlantic Canada Conservation Data Centre ii Table of Contents Table of Contents..........................................................................................................................ii Acknowledgments........................................................................................................................iii Participants....................................................................................................................................4 Background...................................................................................................................................1 Project description ........................................................................................................................1 Methodology.................................................................................................................................2 Results...........................................................................................................................................3 Revised list of rare vascular plants of the Island of Newfoundland .............................................4 Additions to the list of rare vascular plants of the Island of Newfoundland ............................4 Deletions -
The Vegetation and Flora of Auyuittuq National Park Reserve, Baffin Island
THE VEGETATION AND FLORA OF AUYUITTOQ NATIONAL PARK RESERVE, BAFFIN ISLAND ;JAMES E. HINES AND STEVE MOORE DEPARTMENT OF RENEWABLE RESOURCES GOVERNMENT OF THE NORTHWEST TERRITORIES YELLOWKNIFE I NORTHWEST TERRITORIES I XlA 2L9 1988 A project completed under contract to Environment Canada, Canadian Parks Service, Prairie and Northern Region, Winnipeg, Manitoba. 0 ~tona Renewable Resources File Report No. 74 Renewabl• R•sources ~ Government of tha N p .0. Box l 310 Ya\lowknif e, NT XlA 2L9 ii! ABSTRACT The purposes of this investigation were to describe the flora and major types of plant communities present in Auyuittuq National Park Reserve, Baffin Island, and to evaluate factors influencing the distribution of the local vegetation. Six major types of plant communities were recognized based on detailed descriptions of the physical environment, flora, and ground cover of shrubs, herbs, bryophytes, ·and lichens at 100 sites. Three highly interrelated variables (elevation, soil moisture, and texture of surficial deposits) seemed to be important in determining the distribution and abundance of plant communities. Continuous vegetation developed mainly at low elevations on mesic to wet, fine-textured deposits. Wet tundra, characterized by abundant cover of shrubs, grasses, sedges, and forbs, occurred most frequently on wet, fine-textured marine and fluvial sediments. Dwarf shrub-qram.inoid comm.unities were comprised of abundant shrubs, grasses, sedges and forbs and were found most frequently below elevations of 400 m on mesic till or colluvial deposits. Dwarf shrub comm.unities were characterized by abundant dwarf shrub and lichen cover. They developed at similar elevations and on similar types of surficial deposits as dwarf-shrub graminoid communities. -
Leaf Photosynthesis and Simulated Carbon Budget of Gentiana
Journal of Plant Ecology Leaf photosynthesis and simulated VOLUME 2, NUMBER 4, PAGES 207–216 carbon budget of Gentiana DECEMBER 2009 doi: 10.1093/jpe/rtp025 straminea from a decade-long Advanced Access published on 20 November 2009 warming experiment available online at www.jpe.oxfordjournals.org Haihua Shen1,*, Julia A. Klein2, Xinquan Zhao3 and Yanhong Tang1 1 Environmental Biology Division, National Institute for Environmental Studies, Onogawa 16-2, Tsukuba, Ibaraki, 305-8506, Japan 2 Department of Forest, Rangeland & Watershed Stewardship, Colorado State University, Fort Collins, CO 80523, USA and 3 Northwest Plateau Institute of Biology, Chinese Academy of Sciences, Xining, Qinghai, China *Correspondence address. Environmental Biology Division, National Institute for Environmental Studies, Onogawa 16-2, Tsukuba, Ibaraki, 305-8506, Japan. Tel: +81-29-850-2481; Fax: 81-29-850-2483; E-mail: [email protected] Abstract Aims 2) Despite the small difference in the temperature environ- Alpine ecosystems may experience larger temperature increases due ment, there was strong tendency in the temperature acclima- to global warming as compared with lowland ecosystems. Informa- tion of photosynthesis. The estimated temperature optimum of tion on physiological adjustment of alpine plants to temperature light-saturated photosynthetic CO2 uptake (Amax) shifted changes can provide insights into our understanding how these ;1°C higher from the plants under the ambient regime to plants are responding to current and future warming. We tested those under the OTCs warming regime, and the Amax was sig- the hypothesis that alpine plants would exhibit acclimation in pho- nificantly lower in the warming-acclimated leaves than the tosynthesis and respiration under long-term elevated temperature, leaves outside the OTCs. -
Heathland Wind Farm Technical Appendix A8.1: Habitat Surveys
HEATHLAND WIND FARM TECHNICAL APPENDIX A8.1: HABITAT SURVEYS JANAURY 2021 Prepared By: Harding Ecology on behalf of: Arcus Consultancy Services 7th Floor 144 West George Street Glasgow G2 2HG T +44 (0)141 221 9997 l E [email protected] w www.arcusconsulting.co.uk Registered in England & Wales No. 5644976 Habitat Survey Report Heathland Wind Farm TABLE OF CONTENTS ABBREVIATIONS .................................................................................................................. 1 1 INTRODUCTION ........................................................................................................ 2 1.1 Background .................................................................................................... 2 1.2 Site Description .............................................................................................. 2 2 METHODS .................................................................................................................. 3 2.1 Desk Study...................................................................................................... 3 2.2 Field Survey .................................................................................................... 3 2.3 Survey Limitations .......................................................................................... 5 3 RESULTS .................................................................................................................... 6 3.1 Desk Study..................................................................................................... -
Vivipary, Proliferation, and Phyllody in Grasses
Vivipary, Proliferation, and Phyllody in Grasses A.A. BEETLE Abstract Some temperate grasses have the ability to produce in their tration of the putative flowering hormone is required for inflorescence modified spikelet structures that act to reproduce the flower induction, whereas in the seminiferous races this species vegetatively. These types may be either genetically fixed or difference is not so great. In the viviparous races, the an occasional expression of environmental change. threshold for flower initiation is rarely exceeded so that perfect flowers appear only occasionally, while in the Vivipary sometimes refers to the development of normally seminiferous races, the conditions arise only separable vegetative shoots, as in the case of Poa bulbosa, rarely where an amount of hormone is produced that is wherein florets have been transformed into bulbils. At other sufficient to initiate culms but insufficient to promote times vivipary refers to the germination of an embryo in situ flowering. before the fall of the seed, as in Melocalamus, the fleshy (a) excess water about the roots seeded bamboo from Burma. (b) excess shade Vegetative proliferation refers to the conversion of the (c) high humidity spikelet, above the glumes, into a leafy shoot. These leafy (d) submergence shoots are not usually an effective method of reproduction (e) abrupt changes in moisture, day length, or tempera- in the wild, but are somewhat easier to establish under ture controlled conditions. (f) insufficient vernalization Both vivipary and proliferation may produce (4) True vivipary conspicuously abnormal spikelets which the latin words vivipara and proZifera have been used to describe, usually without any further discrimination than to indicate their Viviparous Races presence. -
Euphorbiaceae)
Polish Botanical Journal 60(2): 147–161, 2015 DOI: 10.1515/pbj-2015-0024 PHYTOGEOGRAPHICAL ANALYSIS OF EUPHORBIA SUBGENUS ESULA (EUPHORBIACEAE) Dmitry V. Geltman Abstract. Euphorbia subg. Esula is one of four major clades within the genus. A geographical analysis of the 466 species in the subgenus is reported here. Every species was assigned to one of 29 geographical elements clustered in ten groups of ele- ments. This geographical analysis showed that the Tethyan group (comprising nine geographical elements) clearly dominates the subgenus and contains 260 species (55.79% of the total number of species). The most numerous geographical elements are Irano-Turanian (105 species) and Mediterranean (85). Other significant groups of elements are Boreal (91 species, 19.54%), East Asian (40 species, 8.58%), Madrean (26 species, 5.58%), Paleotropical (23 species, 4.94%) and South African (16 species, 3.43%). The area of the Tethyan floristic subkingdom is the center of the modern diversity of E. subg. Esula. It is likely that such diversity is the result of intensive speciation that took place during the Eocene–Miocene. Key words: Euphorbia subg. Esula, geographical elements, Irano-Turanian floristic region, Mediterranean floristic region, phytogeographical analysis, Tethyan floristic subkingdom Dmitry V. Geltman, Komarov Botanical Institute of the Russian Academy of Sciences, Prof. Popov Street, 2, St. Petersburg, 197376, Russia; e-mail: [email protected] Introduction genus euphorbia and its taxonomy cantly differ from traditional ones. For subgenus Esula (Riina et al. 2013), 21 sections were ac- The giant genus Euphorbia L. (Euphorbiaceae) re- cepted on the basis of analyses of the combined cently became a subject of detailed phylogenetic and ITS + ndhF dataset (Fig. -
Salix L.) in the European Alps
diversity Review The Evolutionary History, Diversity, and Ecology of Willows (Salix L.) in the European Alps Natascha D. Wagner 1 , Li He 2 and Elvira Hörandl 1,* 1 Department of Systematics, Biodiversity and Evolution of Plants (with Herbarium), University of Goettingen, Untere Karspüle 2, 37073 Göttingen, Germany; [email protected] 2 College of Forestry, Fujian Agriculture and Forestry University, Fuzhou 350002, China; [email protected] * Correspondence: [email protected] Abstract: The genus Salix (willows), with 33 species, represents the most diverse genus of woody plants in the European Alps. Many species dominate subalpine and alpine types of vegetation. Despite a long history of research on willows, the evolutionary and ecological factors for this species richness are poorly known. Here we will review recent progress in research on phylogenetic relation- ships, evolution, ecology, and speciation in alpine willows. Phylogenomic reconstructions suggest multiple colonization of the Alps, probably from the late Miocene onward, and reject hypotheses of a single radiation. Relatives occur in the Arctic and in temperate Eurasia. Most species are widespread in the European mountain systems or in the European lowlands. Within the Alps, species differ eco- logically according to different elevational zones and habitat preferences. Homoploid hybridization is a frequent process in willows and happens mostly after climatic fluctuations and secondary contact. Breakdown of the ecological crossing barriers of species is followed by introgressive hybridization. Polyploidy is an important speciation mechanism, as 40% of species are polyploid, including the four endemic species of the Alps. Phylogenomic data suggest an allopolyploid origin for all taxa analyzed Citation: Wagner, N.D.; He, L.; so far. -
Supporting Information
Supporting Information Kier et al. 10.1073/pnas.0810306106 1350 New Caledonia** Cape Region** Polynesia-Micronesia and Eastern Pacific** Atlantic Islands* Queensland tropical rain forests Caribbean Islands** East Melanesian Islands** Taiwan Northern Andes incl. northern Páramo** South American Atlantic Coastal Forests** Philippines** West-Ecuador/Choco* Peruvian/Bolivian Yungas & montane forests* Madagascar & Indian Ocean Islands incl. Socotra** Mountains of SW China** Western Ghats* Sri Lanka* SW Australian Floristic Region** New Guinea Tropical Florida 0 200 400 600 800 1000 Range equivalents per 10,000 km² Fig. S1. Top 20 regions according to the level of endemism richness of vascular plants. Asterisks indicate congruence (**) or large overlap (*) with the biodiversity hotspots by Conservation International (Mittermeier, et al. 2004). Orange bars indicate island regions, green bars mainland regions. Kier et al. www.pnas.org/cgi/content/short/0810306106 1of15 Fig. S2. Endemism richness (range equivalents per 10,000 km2) of terrestrial vertebrates at the ecoregion level of mainland (green) and island regions (orange). Boxes mark second and third quartiles, whiskers the nonoutlier range of the data. (A) Terrestrial vertebrates, (B) amphibians, (C) birds, (D) reptiles, and (E) mammals. Kier et al. www.pnas.org/cgi/content/short/0810306106 2of15 Spearman rank correlation Vascular 0.75 0.82 0.73 0.78 0.83 plants 90 Amphibians 0.76 0.82 0.82 0.87 0 90 Reptiles 0.85 0.85 0.94 ER rank ER rank 0 90 Birds 0.89 0.96 0 90 Mammals 0.94 0 90 Tetrapods ER rank ER rank ER rank 0 090090090090090 ER rank ER rank ER rank ER rank ER rank Fig. -
Chapter 3 MATERIAL and METHODS
Chapter 3 MATERIAL AND METHODS 3.1. Introduction The study of flora consists of plant and situation of plant habitat. There are many definitions for word "flora". The word "flora" refers to the plants occurring within a given region. A Flora may contain anything from a simple list of the plants occurring in an area to a very detailed account of those plants. Floras are different from popular manuals in that they attempt to cover all of the plants, rather than only the most common or conspicuous ones. When a researcher wants to study Flora he/or she can understand many things from that. A Flora ahnost always contains scientific names, and it may also include common names, literature references, descriptions, habitats, geographical distribution, illustrations, flowering times, and notes. Less often, Floras includes such specialized information as data on plant chemistry, reproduction, chromosome numbers, and population occurrences. Sometimes, the plants are listed alphabetically, and sometimes they are represented within a classification system that indicates which plants are most similar or are thought to be related. Floras often also include devices called "keys" that enable the user to identify an unknown plant. Floristic elements are most often defined subjectively by grouping plant ranges into types based on descriptions provided by floras and manuals (McLaughlin and Bowers, 1990). By study of floristic traits of an area, it is possible to describe floristic province and phytogeographical regions. The delimitation of floristic provinces and sub-provinces is mainly based on the distribution boundaries of vascular plant species (Yurtsev, 1994) which is known as true plants. -
Phylogenetic Taxonomy of Artemisia L. Species from Kazakhstan Based On
PROCEEDINGS OF THE LATVIAN ACADEMY OF SCIENCES. Section B, Vol. 72 (2018), No. 1 (712), pp. 29–37. DOI: 10.1515/prolas-2017-0068 PHYLOGENETIC TAXONOMY OF ARTEMISIA L. SPECIES FROM KAZAKHSTAN BASED ON MATK ANALYSES Yerlan Turuspekov1,5, Yuliya Genievskaya1, Aida Baibulatova1, Alibek Zatybekov1, Yuri Kotuhov2, Margarita Ishmuratova3, Akzhunis Imanbayeva4, and Saule Abugalieva1,5,# 1 Institute of Plant Biology and Biotechnology, 45 Timiryazev Street, Almaty, KAZAKHSTAN 2 Altai Botanical Garden, Ridder, KAZAKHSTAN 3 Karaganda State University, Karaganda, KAZAKHSTAN 4 Mangyshlak Experimental Botanical Garden, Aktau, KAZAKHSTAN 5 Al-Farabi Kazakh National University, Biodiversity and Bioresources Department, Almaty, KAZAKHSTAN # Corresponding author, [email protected] Communicated by Isaak Rashal The genus Artemisia is one of the largest of the Asteraceae family. It is abundant and diverse, with complex taxonomic relations. In order to expand the knowledge about the classification of Kazakhstan species and compare it with classical studies, matK genes of nine local species in- cluding endemic were sequenced. The infrageneric rank of one of them (A. kotuchovii) had re- mained unknown. In this study, we analysed results of sequences using two methods — NJ and MP and compared them with a median-joining haplotype network. As a result, monophyletic origin of the genus and subgenus Dracunculus was confirmed. Closeness of A. kotuchovii to other spe- cies of Dracunculus suggests its belonging to this subgenus. Generally, matK was shown as a useful barcode marker for the identification and investigation of Artemisia genus. Key words: Artemisia, Artemisia kotuchovii, DNA barcoding, haplotype network. INTRODUCTION (Bremer, 1994; Torrel et al., 1999). Due to the large amount of species in the genus, their classification is still complex Artemisia of the family Asteraceae is a genus with great and not fully completed. -
Arctic National Wildlife Refuge Volume 2
Appendix F Species List Appendix F: Species List F. Species List F.1 Lists The following list and three tables denote the bird, mammal, fish, and plant species known to occur in Arctic National Wildlife Refuge (Arctic Refuge, Refuge). F.1.1 Birds of Arctic Refuge A total of 201 bird species have been recorded on Arctic Refuge. This list describes their status and abundance. Many birds migrate outside of the Refuge in the winter, so unless otherwise noted, the information is for spring, summer, or fall. Bird names and taxonomic classification follow American Ornithologists' Union (1998). F.1.1.1 Definitions of classifications used Regions of the Refuge . Coastal Plain – The area between the coast and the Brooks Range. This area is sometimes split into coastal areas (lagoons, barrier islands, and Beaufort Sea) and inland areas (uplands near the foothills of the Brooks Range). Brooks Range – The mountains, valleys, and foothills north and south of the Continental Divide. South Side – The foothills, taiga, and boreal forest south of the Brooks Range. Status . Permanent Resident – Present throughout the year and breeds in the area. Summer Resident – Only present from May to September. Migrant – Travels through on the way to wintering or breeding areas. Breeder – Documented as a breeding species. Visitor – Present as a non-breeding species. * – Not documented. Abundance . Abundant – Very numerous in suitable habitats. Common – Very likely to be seen or heard in suitable habitats. Fairly Common – Numerous but not always present in suitable habitats. Uncommon – Occurs regularly but not always observed because of lower abundance or secretive behaviors. -
Why Is the Alpine Flora Comparatively Robust Against Climatic Warming?
diversity Review Why Is the Alpine Flora Comparatively Robust against Climatic Warming? Christian Körner * and Erika Hiltbrunner Department of Environmental Sciences, Botany, University of Basel, Schönbeinstrasse 6, 4056 Basel, Switzerland; [email protected] * Correspondence: [email protected] Abstract: The alpine belt hosts the treeless vegetation above the high elevation climatic treeline. The way alpine plants manage to thrive in a climate that prevents tree growth is through small stature, apt seasonal development, and ‘managing’ the microclimate near the ground surface. Nested in a mosaic of micro-environmental conditions, these plants are in a unique position by a close-by neighborhood of strongly diverging microhabitats. The range of adjacent thermal niches that the alpine environment provides is exceeding the worst climate warming scenarios. The provided mountains are high and large enough, these are conditions that cause alpine plant species diversity to be robust against climatic change. However, the areal extent of certain habitat types will shrink as isotherms move upslope, with the potential areal loss by the advance of the treeline by far outranging the gain in new land by glacier retreat globally. Keywords: biodiversity; high-elevation; mountains; phenology; snow; species distribution; treeline; topography; vegetation; warming Citation: Körner, C.; Hiltbrunner, E. Why Is the Alpine Flora Comparatively Robust against 1. Introduction Climatic Warming? Diversity 2021, 13, The alpine world covers a small land fraction, simply since mountains get narrower 383. https://doi.org/10.3390/ with elevation [1]. Globally, 2.6% of the terrestrial area outside Antarctica meets the criteria d13080383 for ‘alpine’ [2,3], a terrain still including a lot of barren or glaciated areas, with the actual plant covered area closer to 2% (an example for the Eastern Alps in [4]).