Minuartia Hybrida (Vill.) Schischk
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Caryophyllaceae) in Iran
International Journal of Modern Botany 2014, 4(1): 8-21 DOI: 10.5923/j.ijmb.20140401.02 Pollen Micro-morphology of the Minuartia Species (Caryophyllaceae) in Iran Golaleh Mostafavi1,*, Iraj Mehregan2 1Department of Biology, College of Basic Sciences, Yadegar-e-Imam, Khomeini (RAH) Branch, Islamic Azad University, Tehran, Iran 2Department of Biology, Science and Research Branch, Islamic Azad University, Tehran-Iran Abstract The present study compared pollen micro-morphological characters among 20 Iranian Minuartia species. For this purpose, mature pollen grains taken from unopened flowers, were prepared, fixed and exhaustively investigated using Scanning Electron Microscopy (SEM). In order to perform the pollen micro-morphology of Minuartia, and to find its significance in taxonomy of the group, qualitative and quantitative variables related to the shape, size, ornamentations and pores were studied. Cluster and PCA analyses of qualitative and quantitative data were performed to demonstrate the pollen grain similarities among the species. According to our results, Minuartia species exhibit either sub-spherical or polyhedral pollen shapes. Pollen size also varies among different species. The longest polar axis length (P) belongs to Minuartia meyeri Bornm. (34.3±0.26µm) and the smallest one to M. montana L. (15.8±0.26µm). Pore ornamentations differ from prominent granular to slightly or distinctly sunken granular. The number of pores also varies considerably depending on species. It ranges from 10 (in M. meyeri and M. acuminata Turrill) to 24 (in M. subtilis Hand.-Mazz.) on two pollen hemispheres. The most reliable characters in this study were pore diameter (annulus included) (D), equatorial diameter (E), polar axis length (P), the distance between two pores (d), pollen outline, Pore diameter (annulus excluded) (R), annulus diameter (a), P/E ratio, Puncta diameter and Echini diameter respectively. -
Taxonomic Studi Es on Thearenaria Serpyllifolia Group (Caryophyllaceae)
Flora Mediterranea lO - 2000 185 Mohamed N. Abuhadra Taxonomic studies on theArenaria serpyllifolia group (Caryophyllaceae) Abstract Abuhadra, M. N.: Taxonomic studies on the Arenaria serpy//ifolia group (Caryophyllaceae). Fl. Medit. lO : 185-190.2000. - ISSN 1120-4052. Scanning electron microscopic investigation of seed and capsule morphology of Arenaria ser pyllifolia L. and A. leptoclados Guss. In the Caryophy/laceae have been studied. Seed size in both species show consistency, but testa ornamentation (midzone) vary in shape even in the seeds from one capsule of A. serpyfolia, while in A. leptoclados midzone cells are narrowly elongate in different populations and environments. The ripe capsule teeth ornamentation has a diagnosti c character lO separate A. serpy/lifolia and A. leptoclados. lntroduction The group Arenaria serpyllifolia (Caryophyllaceae), includes some taxa, thet in tum has often been considered at specific or subspecific rank. McNeii (1963) regarded seed size as the most satisfactory character separating the tetraploid A. serpyllifolia L. from the diploid A. leptoclados, both automatically self-pollinating species. Perring and Sell (1967) used seed characters but not those of the testa to separate the subspecies lepto clados, serpyllifolia and macrocarpa (Lloyd) Perring & Sell. In the first edition of Flora Europaea A. serpyllifolia and A. leptoclados are treated as species (Charter & Halliday 1964) but in the second they are regarded as subspecies (Charter & Halliday 1993). Greuter & al. (1984) recognised as species the following in the Mediterranean area: A. argaea Rech. f, A. leptoclados (Rchnb.) Guss., A. marschlinsii Koch, A. minutiflora Loscos [doubtful status], A. peloponnesiaca Rech. fil. and A serpyllifolia L .. For Britain Stace (1991), accepts subspecific status: serpyllifolia, leptoclados (Reichenb.) Nyman and Lloydii (Jordan) Bonnier (A . -
Species List For: Valley View Glades NA 418 Species
Species List for: Valley View Glades NA 418 Species Jefferson County Date Participants Location NA List NA Nomination and subsequent visits Jefferson County Glade Complex NA List from Gass, Wallace, Priddy, Chmielniak, T. Smith, Ladd & Glore, Bogler, MPF Hikes 9/24/80, 10/2/80, 7/10/85, 8/8/86, 6/2/87, 1986, and 5/92 WGNSS Lists Webster Groves Nature Study Society Fieldtrip Jefferson County Glade Complex Participants WGNSS Vascular Plant List maintained by Steve Turner Species Name (Synonym) Common Name Family COFC COFW Acalypha virginica Virginia copperleaf Euphorbiaceae 2 3 Acer rubrum var. undetermined red maple Sapindaceae 5 0 Acer saccharinum silver maple Sapindaceae 2 -3 Acer saccharum var. undetermined sugar maple Sapindaceae 5 3 Achillea millefolium yarrow Asteraceae/Anthemideae 1 3 Aesculus glabra var. undetermined Ohio buckeye Sapindaceae 5 -1 Agalinis skinneriana (Gerardia) midwestern gerardia Orobanchaceae 7 5 Agalinis tenuifolia (Gerardia, A. tenuifolia var. common gerardia Orobanchaceae 4 -3 macrophylla) Ageratina altissima var. altissima (Eupatorium rugosum) white snakeroot Asteraceae/Eupatorieae 2 3 Agrimonia pubescens downy agrimony Rosaceae 4 5 Agrimonia rostellata woodland agrimony Rosaceae 4 3 Allium canadense var. mobilense wild garlic Liliaceae 7 5 Allium canadense var. undetermined wild garlic Liliaceae 2 3 Allium cernuum wild onion Liliaceae 8 5 Allium stellatum wild onion Liliaceae 6 5 * Allium vineale field garlic Liliaceae 0 3 Ambrosia artemisiifolia common ragweed Asteraceae/Heliantheae 0 3 Ambrosia bidentata lanceleaf ragweed Asteraceae/Heliantheae 0 4 Ambrosia trifida giant ragweed Asteraceae/Heliantheae 0 -1 Amelanchier arborea var. arborea downy serviceberry Rosaceae 6 3 Amorpha canescens lead plant Fabaceae/Faboideae 8 5 Amphicarpaea bracteata hog peanut Fabaceae/Faboideae 4 0 Andropogon gerardii var. -
GRANITIC FLATROCK (ANNUAL HERB SUBTYPE) Concept: Granitic
GRANITIC FLATROCK (ANNUAL HERB SUBTYPE) Concept: Granitic Flatrock communities are sparsely vegetated or herbaceous communities of flatrock outcrops. The Annual Herb Subtype represents the zones in the vegetation mosaic that occur on the shallowest soil accumulations or on bare rock, where plants are primarily annual herbs, small bryophytes, or lichens. This subtype represents the earliest stages of primary succession. Characteristic flatrock endemic species such as Diamorpha smalli, Sedum pusillum, Portulaca smallii, Mononeuria uniflora, and Cyperus granitophilus occur primarily in this subtype. Distinguishing Features: Granitic Flatrocks are distinguished from Granitic Domes by floristic differences such as the presence of Diamorpha smallii, Sedum pusillum, Mononeuria glabra, Packera tomentosa, Croton willdenowii, and the absence of plants more characteristic of the Blue Ridge, as well as by their location in the central and eastern Piedmont. They are generally distinguished by gentler topography and the associated presence of small weathering depressions, but the range of slopes can overlap with that of Granitic Domes. Granitic Flatrocks are distinguished from all other rock outcrop communities by the characteristic physical structure produced by exfoliation, with shallow depressions but few crevices, fractures, or deeper soil pockets. The Annual Herb Subtype is distinguished from other zones by the dominance of smaller mosses, lichens, or annual herbs, usually Diamorpha, Mononeuria, Sedum, or Portulaca, but also including Hexasepalum (Diodia) teres, Cyperus granitophilus, Hypericum gentianoides, and others. Mats of Grimmia laevigata are included, but beds of Polytrichum spp., Sphagnum spp. beds in seeps, and other larger mosses are included with the Perennial Herb Subtype. Synonyms: Diamorpha smallii - Minuartia glabra - Minuartia uniflora - Cyperus granitophilus Herbaceous Vegetation (CEGL004344). -
Literature Cited Allendorf, F. W. and G. Luikart. 2007. Conservation and the Genetics of Populations. Blackwell Publishing, Ma
Literature Cited Allendorf, F. W. and G. Luikart. 2007. Conservation and the Genetics of Populations. Blackwell Publishing, Malden, Massachusetts. 642 pp. Chester, E. W., B. E. Wofford, D. Estes, and C. Bailey. 2009. A Fifth Checklist of Tennessee Vascular Plants. Botanical Research Institute of Texas Press, Fort Worth, Texas. 102 pp. Dell, N. 2018. Email to Geoff Call, Biologist, U.S. Fish and Wildlife Service re: Mononeuria (=Minuartia) cumberlandensis accessions at Missouri Botanical Garden. Center for Conservation and Sustainable Development, Missouri Botanical Garden, April 25, 2018. Dillenberger, M. S. and J. W. Kadereit. 2014. Multiple origins and delimitation with plesiomorphic characters require a new circumscription of Minuartia (Caryophyllaceae). Taxon 63:64-88. Flora of North America. 2019. http://www.efloras.org. Accessed February 5, 2019. Glick, P., S. Palmer, and J. Wisby. 2015. Climate Change Vulnerability Assessment for Tennessee Wildlife and Habitats. Prepared by National Wildlife Federation and The Nature Conservancy—Tennessee for Tennessee Wildlife Resources Agency, Nashville, Tennessee. 104 pp. Henderson, C. P. 2018. Email to Geoff Call, Biologist, U.S. Fish and Wildlife Service re: TennGreen easements near Big South Fork – Peters Bridge. Director of Land Conservation, Tennessee Parks and Greenways Foundation, May 1, 2018. Heschel, M. S. and K. N. Paige. 1995. Inbreeding depression, environmental stress, and population size variation in scarlet gilia (Ipomopsis aggregata). Conservation Biology 9:126-133. Horton, J. D., 2017. The State Geologic Map Compilation (SGMC) geodatabase of the conterminous United States (ver. 1.1, August 2017): U.S. Geological Survey data release, https://doi.org/10.5066/F7WH2N65. Integrated Taxonomic Information System. -
Interpretation Manual of European Union Habitats-Aprile 2013
INTERPRETATION MANUAL OF EUROPEAN UNION HABITATS EUR 28 April 2013 EUROPEAN COMMISSION DG ENVIRONMENT Nature ENV B.3 The Interpretation Manual of European Union Habitats - EUR28 is a scientific reference document. It is based on the version for EUR15, which was adopted by the Habitats Committee on 4. October 1999 and consolidated with the new and amended habitat types for the 10 accession countries as adopted by the Habitats Committee on 14 March 2002. A small amendment to habitat type 91D0 was adopted by the Habitats Committee in its meeting on 14th October 2003. The Habitats Committee at its meeting on 13 April 2007 adopted additional changes for the accession of Bulgaria and Romania, and for the marine habitats, followed the descriptions given in “Guidelines for the establishment of the Natura 2000 network in the marine environment. Application of the Habitats and Birds Directives” published in May 2007 by the Commission services. Amendments for the accession of Croatia were adopted by the Habitats Committee on 4 October, 2012. The April 2013 version consolidates the changes for Croatia in the text and corrects the references to EUNIS codes for three marine habitat types. TABLE OF CONTENTS WHY THIS MANUAL? 3 HISTORICAL REVIEW 3 THE MANUAL 4 THE EUR15 VERSION 5 THE EUR25 VERSION 5 THE EUR27 VERSION 6 THE EUR28 VERSION 6 EXPLANATORY NOTES 7 COASTAL AND HALOPHYTIC HABITATS 7 COASTAL AND HALOPHYTIC HABITATS 8 OPEN SEA AND TIDAL AREAS 8 SEA CLIFFS AND SHINGLE OR STONY BEACHES 17 ATLANTIC AND CONTINENTAL SALT MARSHES AND SALT MEADOWS 20 -
Flora-Lab-Manual.Pdf
LabLab MManualanual ttoo tthehe Jane Mygatt Juliana Medeiros Flora of New Mexico Lab Manual to the Flora of New Mexico Jane Mygatt Juliana Medeiros University of New Mexico Herbarium Museum of Southwestern Biology MSC03 2020 1 University of New Mexico Albuquerque, NM, USA 87131-0001 October 2009 Contents page Introduction VI Acknowledgments VI Seed Plant Phylogeny 1 Timeline for the Evolution of Seed Plants 2 Non-fl owering Seed Plants 3 Order Gnetales Ephedraceae 4 Order (ungrouped) The Conifers Cupressaceae 5 Pinaceae 8 Field Trips 13 Sandia Crest 14 Las Huertas Canyon 20 Sevilleta 24 West Mesa 30 Rio Grande Bosque 34 Flowering Seed Plants- The Monocots 40 Order Alistmatales Lemnaceae 41 Order Asparagales Iridaceae 42 Orchidaceae 43 Order Commelinales Commelinaceae 45 Order Liliales Liliaceae 46 Order Poales Cyperaceae 47 Juncaceae 49 Poaceae 50 Typhaceae 53 Flowering Seed Plants- The Eudicots 54 Order (ungrouped) Nymphaeaceae 55 Order Proteales Platanaceae 56 Order Ranunculales Berberidaceae 57 Papaveraceae 58 Ranunculaceae 59 III page Core Eudicots 61 Saxifragales Crassulaceae 62 Saxifragaceae 63 Rosids Order Zygophyllales Zygophyllaceae 64 Rosid I Order Cucurbitales Cucurbitaceae 65 Order Fabales Fabaceae 66 Order Fagales Betulaceae 69 Fagaceae 70 Juglandaceae 71 Order Malpighiales Euphorbiaceae 72 Linaceae 73 Salicaceae 74 Violaceae 75 Order Rosales Elaeagnaceae 76 Rosaceae 77 Ulmaceae 81 Rosid II Order Brassicales Brassicaceae 82 Capparaceae 84 Order Geraniales Geraniaceae 85 Order Malvales Malvaceae 86 Order Myrtales Onagraceae -
Zeki Aytaç & Hayri Duman the Steppic Flora of High Mounts Ahir
Zeki Aytaç & Hayri Duman The Steppic flora of high Mounts Ahir, Öksüs and Binboga( (Kahramanmaras, - Kayseri, Turkey) Abstract Aytaç, Z. & Duman, H: The Steppic flora of high Mounts Ahir, Öksüz and Binboga( (Kahramanmaras, - Kayseri, Turkey). — Fl. Medit. 15: 121-178. 2005. — ISSN 1120-4052. The vascular flora of Mts. Ahir, Öksüz and Binboga( in the provinces of Kahramanmaras, and Kayseri (C Anatolia, Turkey B6/C6) has been investigated. 928 specific and infraspecific taxa are listed. 249 (27 %) of them are endemic to Turkey. 372 taxa are Irano-Turanian, 103 Mediterranean, 14 Euro-Siberian elements, 439 multiregional or have not been assessed phyto- ( geographically. 379 taxa are confined to Binboga, 228 to Ahir, and 93 to Öksüz Dagi( and the others for three. Introduction The research areas are located in Kahramanmaras, and Kayseri provinces (Fig. 1). They are within B6 and C6 squares according to the grid system used for Turkish flora. The rea- sons for choosing Ahir, Öksüz and Binboga( Mountains as research area are given as follows: Abundance of endemic plants in this region, its being at the intersection of Mediterranean and Irano-Turanian phytogeographic areas, being on the Anatolian Diagonal. The flora and vegetation of Ahir, Öksüz and Binboga( mountains have not been studied before in detail. Davis and his colleagues collected plant specimens especially from Binboga( Mountain, Haussknechti collected from Berit and Ahir mountains, also Huber- Morath collected from Ahir and Binboga( Mountains (Davis 1965-1988; Davis & al. 2000). Some flora and vegetation studies had been performed in the areas in vicinity to our research area. These areas are as follows: Engizek Mountain (Duman 1990), Berit Mountain (Yildiz 2001), Erciyes Mountain (Çetik 1981, 1985); Bolkar mountains (Gemici 1994). -
Arenaria Serpyllifolia Sensu Been Declared
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Jagiellonian Univeristy Repository Acta Societatis Botanicorum Poloniae DOI: 10.5586/asbp.3630 ORIGINAL RESEARCH PAPER Publication history Received: 2018-08-29 Accepted: 2019-07-18 Is the presence of simple or glandular hairs Published: 2019-09-24 a good trait for distinguishing species in Handling editor Krzysztof Spalik, Faculty of Biology, Biological and Chemical Caryophyllaceae? A case study of Arenaria Research Centre, University of Warsaw, Poland serpyllifolia sensu lato in southern Poland Authors’ contributions KR, MN: idea of the study; MN: project leader; EJ: Kaja Rola, Elżbieta Jędrzejczak, Joanna Zalewska-Gałosz, Marcin morphometric studies; MN: SEM Nobis* studies; KR: statistical analysis; Institute of Botany, Faculty of Biology, Jagiellonian University in Kraków, Gronostajowa 3, 30-387 JZG: molecular analysis; all Kraków, Poland authors helped in preparing the manuscript * Corresponding author. Email: [email protected] Funding The research was funded by the Institute of Botany, Jagiellonian Abstract University in Kraków (K/N18/ Te presence of diferent types of indumentum is regarded as a valuable taxonomic DBS/000002). trait for describing and diferentiating between species in many diferent families Competing interests and genera. In Caryophyllaceae, however, this character is sometimes a subject of No competing interests have discussion and scientifc conficts. For instance, within Arenaria serpyllifolia sensu been declared. lato (s. l.), two or three taxa have been distinguished based on the presence or absence of glandular and/or eglandular hairs on the calyx and uppermost leaves, namely Copyright notice A. serpyllifolia, A. viscida, and A. -
From Cacti to Carnivores: Improved Phylotranscriptomic Sampling And
Article Type: Special Issue Article RESEARCH ARTICLE INVITED SPECIAL ARTICLE For the Special Issue: Using and Navigating the Plant Tree of Life Short Title: Walker et al.—Phylotranscriptomic analysis of Caryophyllales From cacti to carnivores: Improved phylotranscriptomic sampling and hierarchical homology inference provide further insight into the evolution of Caryophyllales Joseph F. Walker1,13, Ya Yang2, Tao Feng3, Alfonso Timoneda3, Jessica Mikenas4,5, Vera Hutchison4, Caroline Edwards4, Ning Wang1, Sonia Ahluwalia1, Julia Olivieri4,6, Nathanael Walker-Hale7, Lucas C. Majure8, Raúl Puente8, Gudrun Kadereit9,10, Maximilian Lauterbach9,10, Urs Eggli11, Hilda Flores-Olvera12, Helga Ochoterena12, Samuel F. Brockington3, Michael J. Moore,4 and Stephen A. Smith1,13 Manuscript received 13 October 2017; revision accepted 4 January 2018. 1 Department of Ecology & Evolutionary Biology, University of Michigan, 830 North University Avenue, Ann Arbor, MI 48109-1048 USA 2 Department of Plant and Microbial Biology, University of Minnesota-Twin Cities, 1445 Gortner Avenue, St. Paul, MN 55108 USA 3 Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, UK 4 Department of Biology, Oberlin College, Science Center K111, 119 Woodland Street, Oberlin, OH 44074-1097 USA 5 Current address: USGS Canyonlands Research Station, Southwest Biological Science Center, 2290 S West Resource Blvd, Moab, UT 84532 USA 6 Institute of Computational and Mathematical Engineering (ICME), Stanford University, 475 Author Manuscript Via Ortega, Suite B060, Stanford, CA, 94305-4042 USA This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. -
1 CV: Snow 2018
1 NEIL SNOW, PH.D. Curriculum Vitae CURRENT POSITION Associate Professor of Botany Curator, T.M. Sperry Herbarium Department of Biology, Pittsburg State University Pittsburg, KS 66762 620-235-4424 (phone); 620-235-4194 (fax) http://www.pittstate.edu/department/biology/faculty/neil-snow.dot ADJUNCT APPOINTMENTS Missouri Botanical Garden (Associate Researcher; 1999-present) University of Hawaii-Manoa (Affiliate Graduate Faculty; 2010-2011) Au Sable Institute of Environmental Studies (2006) EDUCATION Ph.D., 1997 (Population and Evolutionary Biology); Washington University in St. Louis Dissertation: “Phylogeny and Systematics of Leptochloa P. Beauv. sensu lato (Poaceae: Chloridoideae)”. Advisor: Dr. Peter H. Raven. M.S., 1988 (Botany); University of Wyoming. Thesis: “Floristics of the Headwaters Region of the Yellowstone River, Wyoming”. Advisor: Dr. Ronald L. Hartman B.S., 1985 (Botany); Colorado State University. Advisor: Dr. Dieter H. Wilken PREVIOUS POSITIONS 2011-2013: Director and Botanist, Montana Natural Heritage Program, Helena, Montana 2007-2011: Research Botanist, Bishop Museum, Honolulu, Hawaii 1998-2007: Assistant then Associate Professor of Biology and Botany, School of Biological Sciences, University of Northern Colorado 2005 (sabbatical). Project Manager and Senior Ecologist, H. T. Harvey & Associates, Fresno, CA 1997-1999: Senior Botanist, Queensland Herbarium, Brisbane, Australia 1990-1997: Doctoral student, Washington University in St. Louis; Missouri Botanical Garden HERBARIUM CURATORIAL EXPERIENCE 2013-current: Director -
Flora of Australia, Volume 46, Iridaceae to Dioscoreaceae
FLORA OF AUSTRALIA Volume 46 Iridaceae to Dioscoreaceae This volume was published before the Commonwealth Government moved to Creative Commons Licensing. © Commonwealth of Australia 1986. This work is copyright. You may download, display, print and reproduce this material in unaltered form only (retaining this notice) for your personal, non-commercial use or use within your organisation. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced or distributed by any process or stored in any retrieval system or data base without prior written permission from the copyright holder. Requests and inquiries concerning reproduction and rights should be addressed to: [email protected] FLORA OF AUSTRALIA The nine families in this volume of the Flora of Australia are Iridaceae, Aloeaceae, Agavaceae, Xanthorrhoeaceae, Hanguan- aceae, Taccaceae, Stemonaceae, Smilacaceae and Dioscoreaceae. The Xanthorrhoeaceae has the largest representation with 10 genera and 99 species. Most are endemic with a few species of Lomandra and Romnalda extending to neighbouring islands. The family includes the spectacular blackboys and grass-trees. The Iridaceae is largely represented by naturalised species with 52 of the 78 species being introduced. Many of the introductions are ornamentals and several have become serious weeds. Patersonia is the largest genus with all 17 species endemic. Some of these are cultivated as ornamentals. The Dioscoreaccae is a family of economic significance, particularly in the old world tropics where some species are cultivated or collected for their tubers and bulbils. In Australia there are 5 species, one of which is a recent introduction. The endemic and native species, commonly known as yams, are traditionally eaten by the Aborigines.