Relation Between Soil Salinity and Species Composition of Halophytic Plant Communities: a Baseline Data Inventory for Wetland Monitoring
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Seed Germination of the Halophyte Anabasis Setifera (Amaranthaceae) from Saudi Arabia
Botany Seed germination of the halophyte Anabasis setifera (Amaranthaceae) from Saudi Arabia. Journal: Botany Manuscript ID cjb-2018-0053.R1 Manuscript Type: Article Date Submitted by the Author: 19-May-2018 Complete List of Authors: Basahi, Mohammed; Shaqra University College of Science and Arts Sajir, biology; Anabasis setifera,Draft halophyte, Temperature, Germination, seed germination Keyword: recovery Is the invited manuscript for consideration in a Special Not applicable (regular submission) Issue? : https://mc06.manuscriptcentral.com/botany-pubs Page 1 of 27 Botany Seed germination of the halophyte Anabasis setifera (Amaranthaceae) from Saudi Arabia. Mohammed A Basahi College of Science and Arts Sajir Shaqra University P.O. Box 33, Shaqra 11961 Saudi Arabia [email protected] Draft00966582223689 1 https://mc06.manuscriptcentral.com/botany-pubs Botany Page 2 of 27 Abstract The main objective of this study was to determine the effects of temperature, light/darkness, and salinity (NaCl) on seed germination of Anabasis setifera Moq. and the effects of alleviating salinity stress using distilled water. One-hundred percent of seeds completed germination at 15/5, 20/10, and 20°C, and a higher percentage of seeds completed germinationin light than in the dark at 20/10 and 25/15°C. The percentage of seeds that completed the germination decreased as salinity increased from 0 to 700 mM NaCl. Seeds that did not complete germination in the 800 or 700 mM NaCl solutions completed its germinationDraft after being transferred to distilled water, with a recovery rate of 94.5% and 75.5%, respectively, at 25/15°C. The inhibitory effect of NaCl on the completion of germination in this species probably occurs via an osmotic effect. -
5. KALIDIUM Moquin-Tandon in Candolle, Prodr. 13(2): 46, 146
Flora of China 5: 355-356. 2003. 5. KALIDIUM Moquin-Tandon in Candolle, Prodr. 13(2): 46, 146. 1849. 盐爪爪属 yan zhua zhua shu Shrubs small, much branched; branches not jointed. Leaves alternate, terete or undeveloped, fleshy, basally decurrent. Inflorescence pedunculate, spicate. Flowers spirally arranged, (1 or)3 borne in axil of a fleshy bract, appearing sunken into fleshy rachis, without bractlets, bisexual. Perianth 4- or 5-lobed, spongy in fruit, flat on top surface. Stamens 2. Ovary ovoid; stigmas 2, papillate. Fruit a utricle, enclosed by perianth. Seed vertical, compressed; testa subleathery; embryo semi-annular; perisperm present. Five species: C and SW Asia, SE Europe; five species in China. 1a. Leaves 4–10 mm; spikes 3–4 mm in diam. .................................................................................................................... 1. K. foliatum 1b. Leaves less than 3 mm or undeveloped; spikes 1.5–3 mm in diam. 2a. Branchlets slender; flowers 1 per bract ..................................................................................................................... 5. K. gracile 2b. Branchlets stout; flowers 3 per bract. 3a. Leaves developed, 1–3 mm, ovate, adaxially curved, apex acute ............................................................... 2. K. cuspidatum 3b. Leaves undeveloped, tuberculate, less than 1 mm, apex obtuse. 4a. Plants 10–25 cm tall, branched from base; leaves of branchlets narrow and obconic at base ......... 3. K. schrenkianum 4b. Plants 20–70 cm tall, branched from middle; leaves of branchlets sheathing at base ............................ 4. K. caspicum 1. Kalidium foliatum (Pallas) Moquin-Tandon in Candolle, 1b. Leaves 1–1.5 mm; plants densely Prodr. 13(2): 147. 1849. branched .................................................... 2b. var. sinicum 盐爪爪 yan zhua zhua 2a. Kalidium cuspidatum var. cuspidatum Salicornia foliata Pallas, Reise Russ. Reich. 1: 482. -
Towards an Updated Checklist of the Libyan Flora
Towards an updated checklist of the Libyan flora Article Published Version Creative Commons: Attribution 3.0 (CC-BY) Open access Gawhari, A. M. H., Jury, S. L. and Culham, A. (2018) Towards an updated checklist of the Libyan flora. Phytotaxa, 338 (1). pp. 1-16. ISSN 1179-3155 doi: https://doi.org/10.11646/phytotaxa.338.1.1 Available at http://centaur.reading.ac.uk/76559/ It is advisable to refer to the publisher’s version if you intend to cite from the work. See Guidance on citing . Published version at: http://dx.doi.org/10.11646/phytotaxa.338.1.1 Identification Number/DOI: https://doi.org/10.11646/phytotaxa.338.1.1 <https://doi.org/10.11646/phytotaxa.338.1.1> Publisher: Magnolia Press All outputs in CentAUR are protected by Intellectual Property Rights law, including copyright law. Copyright and IPR is retained by the creators or other copyright holders. Terms and conditions for use of this material are defined in the End User Agreement . www.reading.ac.uk/centaur CentAUR Central Archive at the University of Reading Reading’s research outputs online Phytotaxa 338 (1): 001–016 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2018 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.338.1.1 Towards an updated checklist of the Libyan flora AHMED M. H. GAWHARI1, 2, STEPHEN L. JURY 2 & ALASTAIR CULHAM 2 1 Botany Department, Cyrenaica Herbarium, Faculty of Sciences, University of Benghazi, Benghazi, Libya E-mail: [email protected] 2 University of Reading Herbarium, The Harborne Building, School of Biological Sciences, University of Reading, Whiteknights, Read- ing, RG6 6AS, U.K. -
Mohamad Al Hassan
Comparative Analyses of Plant Responses to Drought and Salt Stress in Related Taxa: A Useful Approach to Study Stress Tolerance Mechanisms Mohamad Al Hassan Supervisors: Oscar Vicente Meana Monica Tereza Boscaiu Neagu Valencia, January 2016 Alas, my 3 years journey has come to end, and I find myself in front of the challenging task to summarize my gratitude to those who made this experience end happily. To Pr. Oscar Vicente Meana, a supervisor, a teacher, and forever a good friend. Even before I had the chance to prove myself, you believed in me and gave me a lot of your trust. During these 3 years, I was blessed with your guidance and care that allowed me to attain the aimed title with outmost professionalism, while having the chance to follow my instincts. It is said that “The Mediocre Teacher Tells. The Good Teacher Explains. The Superior Teacher Demonstrates. The Great Teacher Inspires”, and you sir, were and always will be a source of inspiration. I will forever be proud that I was your student. To Dr. Mónica Tereza Boscaiu Neagu, a director, a teacher, and forever a good friend. You were always a great support in every step of this work. Thank you for your trust, guidance and care. I am forever in your debt and will always be proud to have been your student one day. To Dr. Federico Martinelli, a colleague and forever a good friend. Thank you for your time, help and support whenever needed, you are a special person, and I hope that what you and Cristian aspire for, gets fulfilled very soon. -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
CHENOPODIACEAE 藜科 Li Ke Zhu Gelin (朱格麟 Chu Ge-Ling)1; Sergei L
Flora of China 5: 351-414. 2003. CHENOPODIACEAE 藜科 li ke Zhu Gelin (朱格麟 Chu Ge-ling)1; Sergei L. Mosyakin2, Steven E. Clemants3 Herbs annual, subshrubs, or shrubs, rarely perennial herbs or small trees. Stems and branches sometimes jointed (articulate); indumentum of vesicular hairs (furfuraceous or farinose), ramified (dendroid), stellate, rarely of glandular hairs, or plants glabrous. Leaves alternate or opposite, exstipulate, petiolate or sessile; leaf blade flattened, terete, semiterete, or in some species reduced to scales. Flowers monochlamydeous, bisexual or unisexual (plants monoecious or dioecious, rarely polygamous); bracteate or ebracteate. Bractlets (if present) 1 or 2, lanceolate, navicular, or scale-like. Perianth membranous, herbaceous, or succulent, (1–)3–5- parted; segments imbricate, rarely in 2 series, often enlarged and hardened in fruit, or with winged, acicular, or tuberculate appendages abaxially, seldom unmodified (in tribe Atripliceae female flowers without or with poorly developed perianth borne between 2 specialized bracts or at base of a bract). Stamens shorter than or equaling perianth segments and arranged opposite them; filaments subulate or linear, united at base and usually forming a hypogynous disk, sometimes with interstaminal lobes; anthers dorsifixed, incumbent in bud, 2-locular, extrorse, or dehiscent by lateral, longitudinal slits, obtuse or appendaged at apex. Ovary superior, ovoid or globose, of 2–5 carpels, unilocular; ovule 1, campylotropous; style terminal, usually short, with 2(–5) filiform or subulate stigmas, rarely capitate, papillose, or hairy on one side or throughout. Fruit a utricle, rarely a pyxidium (dehiscent capsule); pericarp membranous, leathery, or fleshy, adnate or appressed to seed. Seed horizontal, vertical, or oblique, compressed globose, lenticular, reniform, or obliquely ovoid; testa crustaceous, leathery, membranous, or succulent; embryo annular, semi-annular, or spiral, with narrow cotyledons; endosperm much reduced or absent; perisperm abundant or absent. -
Common Edible Seaweeds in the Gulf of Alaska
eliciousor millennia, Alaska edible Natives have seaweedssubsisted COMMON EDIBLE Don the wild edibles—plants, animals, and F seaweeds—found in abundance along Alaska’s shores. In this book, Dr. Dolly Garza, a Haida-Tlingit Indian, shows you how to look for, identify, harvest, preserve, and prepare several species of seaweeds SEAWEEDS and one plant for tasty snacks or for the dinner table. IN THE GULF OF ALASKA A University of Alaska Fairbanks professor emerita, Dolly was raised in southeast Alaska Second Edition where her family routinely harvested seaweeds as a diet staple, a practice they continue today. Dolly enjoys sharing her traditional Native knowledge through presentations to Elderhostel groups, youth groups, and others. In this book she shares with you her lifetime of first-hand knowledge about the pleasures of harvesting, preparing, and eating some of the most common and delectable wild edibles found along Gulf of Alaska shores. US $10.00 CAN $10.00 DOLLY GARZA Seaweeds book cover.indd 1 3/28/12 9:30 AM COMMON EDIBLE SEAWEEDS IN THE GULF OF ALASKA Second Edition DOLLY GARZA Published by Alaska Sea Grant, University of Alaska Fairbanks SG-ED-46 Elmer E. Rasmuson Library Cataloging in Publication Data Garza, Dolly A. Common edible seaweeds in the Gulf of Alaska / Dolly Garza. — Fair- banks, Alaska : Alaska Sea Grant College Program, University of Alaska Fairbanks. p. : ill. ; cm. - (Alaska Sea Grant College Program, University of Alaska Fairbanks ; SG-ED-46) 1. Marine algae as food—Alaska—Alaska, Gulf of. 2. Cookery (Marine algae) I. Title. II. Series: Alaska Sea Grant College Program, University of Alaska Fairbanks ; SG-ED-46. -
Molecular Systematics of Genus Atractylodes (Compositae, Cardueae): Evidence from Internal Transcribed Spacer (ITS) and Trnl-F Sequences
Int. J. Mol. Sci. 2012, 13, 14623-14633; doi:10.3390/ijms131114623 OPEN ACCESS International Journal of Molecular Sciences ISSN 1422-0067 www.mdpi.com/journal/ijms Article Molecular Systematics of Genus Atractylodes (Compositae, Cardueae): Evidence from Internal Transcribed Spacer (ITS) and trnL-F Sequences Hua-Sheng Peng 1,2, Qing-Jun Yuan 1, Qian-Quan Li 1 and Lu-Qi Huang 1,* 1 Institute of Chinese Materia Medica, China Academy of Chinese Medical Science, Beijing 100700, China; E-Mails: [email protected] (H.-S.P.); [email protected] (Q.-J.Y.); [email protected] (Q.-Q.L.) 2 Department of Pharmacy, Anhui University of Traditional Chinese Medicine, Hefei 230031, China * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +86-10-8404-4340. Received: 13 August 2012; in revised form: 26 October 2012 / Accepted: 30 October 2012 / Published: 9 November 2012 Abstract: To determine the evolutionary relationships among all members of the genus Atractylodes (Compositae, Cardueae), we conducted molecular phylogenetic analyses of one nuclear DNA (nrDNA) region (internal transcribed spacer, ITS) and one chloroplast DNA (cpDNA) region (intergenic spacer region of trnL-F). In ITS and ITS + trnL-F trees, all members of Atractylodes form a monophyletic clade. Atractylodes is a sister group of the Carlina and Atractylis branch. Atractylodes species were distributed among three clades: (1) A. carlinoides (located in the lowest base of the Atractylodes phylogenetic tree), (2) A. macrocephala, and (3) the A. lancea complex, including A. japonica, A. coreana, A. lancea, A. lancea subsp. luotianensis, and A. chinensis. The taxonomic controversy over the classification of species of Atractylodes is mainly concentrated in the A. -
Liste Plantes
Plantes Quantité Acacia angustissima (Fabaceae) Acacia farnesiana Acacia greggii Acanthophyllum pungens (Caryophyllaceae) Acanthus hirsurtus subsp.syriacus (Acanthaceae) Acanthus mollis Acanthus spinosus Acanthus spinosus subsp.spinosissimus Adenocarpus decorticans (Fabaceae) Adenostoma fasciculatum (Rosaceae) Agave parryi var. truncata (Agavaceae) Aloysia gratissima (Verbenaceae) Amygdalus orientalis (Rosaceae) Anisacanthus quadrifidus subsp. wrightii (Acanthaceae) Anisacanthus thurberii Anthirrhinum charidemi (Plantaginaceae) Anthyllis hermanniae (Fabaceae) Aphyllanthes monspeliensis (Liliaceae) Arbutus andrachne (Ericaceae) Arbutus menziesii Arbutus unedo Arbutus x andrachnoïdes Arbutus x thuretiana Arbutus xalapensis subsp. texana Arbutus-xalapensis-subsp. -arizonica Arctostaphylos (Ericaceae) Arctostaphylos canescens subsp. canescens Arctostaphylos glandulosa subsp. glandulosa Arctostaphylos glauca Arctostaphylos manzanita Arctostaphylos pringlei subsp. pringlei Arctostaphylos pungens Argania spinosa (Sapotaceae) Argyrocytisus battandieri ( Leguminosae) Aristolochia baetica ( Aristolochiaceae) Aristolochia californica Aristolochia chilensis Aristolochia parvifolia Aristolochia pistolochia Aristolochia rotunda Aristolochia sempervirens Artemisia alba (Compositae) Artemisia alba var. canescens Artemisia arborescens Artemisia caerulescens subsp. gallica Artemisia californica Artemisia cana Artemisia cana subsp. bolanderi Artemisia herba-alba Artemisia tridentata subsp. nova Artemisia tridentata subsp. tridentata Artemisia tridentata -
Nuclear and Plastid DNA Phylogeny of the Tribe Cardueae (Compositae
1 Nuclear and plastid DNA phylogeny of the tribe Cardueae 2 (Compositae) with Hyb-Seq data: A new subtribal classification and a 3 temporal framework for the origin of the tribe and the subtribes 4 5 Sonia Herrando-Morairaa,*, Juan Antonio Callejab, Mercè Galbany-Casalsb, Núria Garcia-Jacasa, Jian- 6 Quan Liuc, Javier López-Alvaradob, Jordi López-Pujola, Jennifer R. Mandeld, Noemí Montes-Morenoa, 7 Cristina Roquetb,e, Llorenç Sáezb, Alexander Sennikovf, Alfonso Susannaa, Roser Vilatersanaa 8 9 a Botanic Institute of Barcelona (IBB, CSIC-ICUB), Pg. del Migdia, s.n., 08038 Barcelona, Spain 10 b Systematics and Evolution of Vascular Plants (UAB) – Associated Unit to CSIC, Departament de 11 Biologia Animal, Biologia Vegetal i Ecologia, Facultat de Biociències, Universitat Autònoma de 12 Barcelona, ES-08193 Bellaterra, Spain 13 c Key Laboratory for Bio-Resources and Eco-Environment, College of Life Sciences, Sichuan University, 14 Chengdu, China 15 d Department of Biological Sciences, University of Memphis, Memphis, TN 38152, USA 16 e Univ. Grenoble Alpes, Univ. Savoie Mont Blanc, CNRS, LECA (Laboratoire d’Ecologie Alpine), FR- 17 38000 Grenoble, France 18 f Botanical Museum, Finnish Museum of Natural History, PO Box 7, FI-00014 University of Helsinki, 19 Finland; and Herbarium, Komarov Botanical Institute of Russian Academy of Sciences, Prof. Popov str. 20 2, 197376 St. Petersburg, Russia 21 22 *Corresponding author at: Botanic Institute of Barcelona (IBB, CSIC-ICUB), Pg. del Migdia, s. n., ES- 23 08038 Barcelona, Spain. E-mail address: [email protected] (S. Herrando-Moraira). 24 25 Abstract 26 Classification of the tribe Cardueae in natural subtribes has always been a challenge due to the lack of 27 support of some critical branches in previous phylogenies based on traditional Sanger markers. -
A Formal Classification of the Lygeum Spartum Vegetation of the Mediterranean Region
DR. CORRADO MARCENÒ (Orcid ID : 0000-0003-4361-5200) Article type : Research article Florian Jansen Coordinating Editor: Prof. Florian Jansen A formal classification of the Lygeum spartum vegetation of the Mediterranean Region Corrado Marcenò1, Riccardo Guarino2, Ladislav Mucina3, Idoia Biurrun1, Ulrich Deil4, Kamal Shaltout5, Manfred Finckh6, Xavier Font 7, Javier Loidi1 1 Department of Plant Biology and Ecology, University of the Basque Country UPV/EHU, Bilbao, 48080, Spain 2 Department of Biological, Chemical and Pharmaceutical Sciences, and Technologies, University of Palermo, Palermo, 90128, Italy 3 Harry Butler Institute, Murdoch University, 90 South Street, Murdoch 6150, Perth, Australia; Department of Geography and Environmental Studies, Stellenbosch University, Private Bag X1, Matieland 7602, Stellenbosch, South Africa 4 Department of Geobotany, Faculty of Biology, University of Freiburg, 79104 Freiburg i. Br., Germany 5 Faculty of Science, Tanta University, Tanta, 31527, Egypt 6 Biodiversity, Ecology and Evolution of Plants, Institute for Plant Science and Microbiology, University of Hamburg, 22609, Hamburg, Germany 7Plant Biodiversity Resource Centre, University of Barcelona, 08028, Barcelona, Spain This article has been accepted for publication and 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. Please cite this article as doi: 10.1111/avsc.12456 This article is protected by copyright. All rights reserved ORCID Corrado Marcenò: 0000-0003-4361-5200 Riccardo Guarino: 0000-0003-0106-9416 Ladislav Mucina: 0000-0003-0317-8886 Idoia Biurrun: 0000-0002-1454-0433 Manfred Finckh: 0000-0003-2186-0854 Xavier Font: 0000-0002-7253-8905 Javier Loidi: 0000-0003-3163-2409 Correspondence Corrado Marcenò, Department of Plant Biology and Ecology, University of the Basque Country UPV/EHU, Bilbao, 48080, Spain Email: [email protected] Funding information CM, IB and JL were funded by the Basque Government (IT936-16). -
Salicornia L., Chenopodiaceae)
TAXON 56 (4) • November 2007: 1143–1170 Kadereit & al. • Phylogeny and biogeography of Salicornia A taxonomic nightmare comes true: phylogeny and biogeography of glassworts (Salicornia L., Chenopodiaceae) Gudrun Kadereit1*, Peter Ball2, Svetlana Beer3, Ladislav Mucina4, Dmitry Sokoloff 5, Patrick Teege1, Ahmet E. Yaprak5 & Helmut Freitag6 1 Institut für Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universität Mainz, 55099 Mainz, Germany 2 Biology Department, University of Toronto at Mississauga, Mississauga, Ontario, L5L 1C6, Canada 3 Higher Plants Department, Moscow State University, 119992 Moscow, Russia 4 Dept. of Botany & Zoology, Evolutionary Plant Biology & Conservation Group, Stellenbosch University, 7602 Matieland, South Africa 5 Ankara University, Science Faculty, Department of Biology, Besevler/Ankara, Turkey 6 Arbeitsgruppe Systematik und Morphologie der Pflanzen, Universität Kassel, 34109 Kassel, Germany * Author for correspondence ([email protected]) In this study we analysed ETS sequence data of 164 accessions belonging to 31 taxa of Salicornia, a wide- spread, hygrohalophytic genus of succulent, annual herbs of Chenopodiaceae subfam. Salicornioideae, to investigate phylogenetic and biogeographical patterns and hypothesise about the processes that shaped them. Furthermore, our aim was to understand the reasons for the notorious taxonomic difficulties in Salicornia. Salicornia probably originated during the Miocene somewhere between the Mediterranean and Central Asia from within the perennial Sarcocornia