Plant Composition of a Pasture As a Predictor of Soil Salinity
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Density, Distribution and Habitat Requirements for the Ozark Pocket Gopher (Geomys Bursarius Ozarkensis)
DENSITY, DISTRIBUTION AND HABITAT REQUIREMENTS FOR THE OZARK POCKET GOPHER (Geomys bursarius ozarkensis) Audrey Allbach Kershen, B. S. Thesis Prepared for the Degree of MASTER OF SCIENCE UNIVERSITY OF NORTH TEXAS May 2004 APPROVED: Kenneth L. Dickson, Co-Major Professor Douglas A. Elrod, Co-Major Professor Thomas L. Beitinger, Committee Member Sandra L. Terrell, Interim Dean of the Robert B. Toulouse School of Graduate Studies Kershen, Audrey Allbach, Density, distribution and habitat requirements for the Ozark pocket gopher (Geomys bursarius ozarkensis). Master of Science (Environmental Science), May 2004, 67 pp., 6 tables, 6 figures, 69 references. A new subspecies of the plains pocket gopher (Geomys bursarius ozarkensis), located in the Ozark Mountains of north central Arkansas, was recently described by Elrod et al. (2000). Current range for G. b. ozarkensis was established, habitat preference was assessed by analyzing soil samples, vegetation and distance to stream and potential pocket gopher habitat within the current range was identified. A census technique was used to estimate a total density of 3, 564 pocket gophers. Through automobile and aerial survey 51 known fields of inhabitance were located extending the range slightly. Soil analyses indicated loamy sand as the most common texture with a slightly acidic pH and a broad range of values for other measured soil parameters and 21 families of vegetation were identified. All inhabited fields were located within an average of 107.2m from waterways and over 1,600 hectares of possible suitable habitat was identified. ACKNOWLEDGMENTS Appreciation is extended to the members of my committee, Dr. Kenneth Dickson, Dr. Douglas Elrod and Dr. -
Arxiv:1508.05435V1 [Physics.Bio-Ph]
Fast nastic motion of plants and bio-inspired structures Q. Guo1,2, E. Dai3, X. Han4, S. Xie5, E. Chao3, Z. Chen4 1College of Materials Science and Engineering, FuJian University of Technology, Fuzhou 350108, China 2Fujian Provincial Key Laboratory of Advanced Materials Processing and Application, Fuzhou 350108, China 3Department of Biomedical Engineering, Washington University, St. Louis, MO 63130 USA 4Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire, NH 03755, USA 5Department of Energy, Environmental, and Chemical Engineering, Washington University, St. Louis, MO 63130 USA ∗ (Dated: August 25, 2015) The capability to sense and respond to external mechanical stimuli at various timescales is es- sential to many physiological aspects in plants, including self-protection, intake of nutrients, and reproduction. Remarkably, some plants have evolved the ability to react to mechanical stimuli within a few seconds despite a lack of muscles and nerves. The fast movements of plants in response to mechanical stimuli have long captured the curiosity of scientists and engineers, but the mechanisms behind these rapid thigmonastic movements still are not understood completely. In this article, we provide an overview of such thigmonastic movements in several representative plants, including Dionaea, Utricularia, Aldrovanda, Drosera, and Mimosa. In addition, we review a series of studies that present biomimetic structures inspired by fast moving plants. We hope that this article will shed light on the current status of research on the fast movements of plants and bioinspired struc- tures and also promote interdisciplinary studies on both the fundamental mechanisms of plants’ fast movements and biomimetic structures for engineering applications, such as artificial muscles, multi-stable structures, and bioinspired robots. -
MSRP Appendix E
Appendix E. Exotic Plant Species Reported from the South Florida Ecosystem. Community types are indicated where known Species High Pine Scrub Scrubby high pine Beach dune/ Coastal strand Maritime hammock Mesic temperate hammock Tropical hardwood Pine rocklands Scrubby flatwoods Mesic pine flatwoods Hydric pine flatwoods Dry prairie Cutthroat grass Wet prairie Freshwater marsh Seepage swamp Flowing water swamp Pond swamp Mangrove Salt marsh Abelmoschus esculentus Abrus precatorius X X X X X X X X X X X X Abutilon hirtum Abutilon theophrasti Acacia auriculiformis X X X X X X X X X Acacia retinoides Acacia sphaerocephala Acalypha alopecuroidea Acalypha amentacea ssp. wilkesiana Acanthospermum australe Acanthospermum hispidum Achyranthes aspera var. X aspera Achyranthes aspera var. pubescens Acmella pilosa Page E-1 Species High Pine Scrub Scrubby high pine Beach dune/ Coastal strand Maritime hammock Mesic temperate hammock Tropical hardwood Pine rocklands Scrubby flatwoods Mesic pine flatwoods Hydric pine flatwoods Dry prairie Cutthroat grass Wet prairie Freshwater marsh Seepage swamp Flowing water swamp Pond swamp Mangrove Salt marsh Acrocomia aculeata X Adenanthera pavonina X X Adiantum anceps X Adiantum caudatum Adiantum trapeziforme X Agave americana Agave angustifolia cv. X marginata Agave desmettiana Agave sisalana X X X X X X Agdestis clematidea X Ageratum conyzoides Ageratum houstonianum Aglaonema commutatum var. maculatum Ailanthus altissima Albizia julibrissin Albizia lebbeck X X X X X X X Albizia lebbeckoides Albizia procera Page -
Grass Genera in Townsville
Grass Genera in Townsville Nanette B. Hooker Photographs by Chris Gardiner SCHOOL OF MARINE and TROPICAL BIOLOGY JAMES COOK UNIVERSITY TOWNSVILLE QUEENSLAND James Cook University 2012 GRASSES OF THE TOWNSVILLE AREA Welcome to the grasses of the Townsville area. The genera covered in this treatment are those found in the lowland areas around Townsville as far north as Bluewater, south to Alligator Creek and west to the base of Hervey’s Range. Most of these genera will also be found in neighbouring areas although some genera not included may occur in specific habitats. The aim of this book is to provide a description of the grass genera as well as a list of species. The grasses belong to a very widespread and large family called the Poaceae. The original family name Gramineae is used in some publications, in Australia the preferred family name is Poaceae. It is one of the largest flowering plant families of the world, comprising more than 700 genera, and more than 10,000 species. In Australia there are over 1300 species including non-native grasses. In the Townsville area there are more than 220 grass species. The grasses have highly modified flowers arranged in a variety of ways. Because they are highly modified and specialized, there are also many new terms used to describe the various features. Hence there is a lot of terminology that chiefly applies to grasses, but some terms are used also in the sedge family. The basic unit of the grass inflorescence (The flowering part) is the spikelet. The spikelet consists of 1-2 basal glumes (bracts at the base) that subtend 1-many florets or flowers. -
The Ppz Protein Phosphatases Are Key Regulators of K+ and Ph Homeostasis: Implications for Salt Tolerance, Cell Wall Integrity and Cell Cycle Progression
The EMBO Journal Vol. 21 No. 5 pp. 920±929, 2002 The Ppz protein phosphatases are key regulators of K+ and pH homeostasis: implications for salt tolerance, cell wall integrity and cell cycle progression Lynne Yenush, Jose M.Mulet, but the mechanisms that regulate their activity to achieve JoaquõÂn ArinÄ o1 and Ramo n Serrano2 cation homeostasis are only starting to be elucidated (Serrano and Rodriguez-Navarro, 2001). Instituto de BiologõÂa Molecular y Celular de Plantas, Universidad PoliteÂcnica de Valencia-CSIC, Camino de Vera s/n, Several lines of evidence have indicated the existence of E-46022 Valencia and 1Departament de BioquõÂmica i Biologia a link between cation homeostasis and the cell cycle. Molecular, Fac. VeterinaÁria, Universitat AutoÁnoma de Barcelona, Speci®cally, previous studies have established a correl- Bellaterra 08193, Barcelona, Spain ation between cytosolic alkalinization and G1 progression 2Corresponding author in yeast (Gillies et al., 1981) and animal cells (Nuccitelli e-mail: [email protected] and Heiple, 1982). This increased intracellular pH may be either a regulatory signal (Perona and Serrano, 1988) or The yeast Ppz protein phosphatases and the Hal3p merely permissive for cell proliferation (Grinstein et al., inhibitory subunit are important determinants of salt 1989). More recently, in the eukaryotic model system tolerance, cell wall integrity and cell cycle progression. Saccharomyces cerevisiae, alterations in the expression of We present several lines of evidence showing that several genes encoding signal transduction proteins have these disparate phenotypes are connected by the fact been shown to affect both intracellular ion homeostasis that Ppz regulates K+ transport. First, salt tolerance, and cell cycle, again suggesting a possible link between cell wall integrity and cell cycle phenotypes of Ppz these two highly regulated cellular processes. -
Conservation of Grassland Plant Genetic Resources Through People Participation
University of Kentucky UKnowledge International Grassland Congress Proceedings XXIII International Grassland Congress Conservation of Grassland Plant Genetic Resources through People Participation D. R. Malaviya Indian Grassland and Fodder Research Institute, India Ajoy K. Roy Indian Grassland and Fodder Research Institute, India P. Kaushal Indian Grassland and Fodder Research Institute, India Follow this and additional works at: https://uknowledge.uky.edu/igc Part of the Plant Sciences Commons, and the Soil Science Commons This document is available at https://uknowledge.uky.edu/igc/23/keynote/35 The XXIII International Grassland Congress (Sustainable use of Grassland Resources for Forage Production, Biodiversity and Environmental Protection) took place in New Delhi, India from November 20 through November 24, 2015. Proceedings Editors: M. M. Roy, D. R. Malaviya, V. K. Yadav, Tejveer Singh, R. P. Sah, D. Vijay, and A. Radhakrishna Published by Range Management Society of India This Event is brought to you for free and open access by the Plant and Soil Sciences at UKnowledge. It has been accepted for inclusion in International Grassland Congress Proceedings by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Conservation of grassland plant genetic resources through people participation D. R. Malaviya, A. K. Roy and P. Kaushal ABSTRACT Agrobiodiversity provides the foundation of all food and feed production. Hence, need of the time is to collect, evaluate and utilize the biodiversity globally available. Indian sub-continent is one of the world’s mega centers of crop origins. India possesses 166 species of agri-horticultural crops and 324 species of wild relatives. -
Recognise the Important Grasses
Recognise the important grasses Desirable perennial grasses Black speargrass Heteropogon contortus - Birdwood buffel Cenchrus setiger Buffel grass Cenchrus ciliaris Cloncury buffel Cenchrus pennisetijormis Desert bluegrass Bothriochloa ewartiana - Forest bluegrass Bothriochloa bladhii - Giant speargrass Heteropogon triticeus - Gulf or curly bluegrass Dichanthiumjecundum - Indian couch Bothriochloa pertusa + Kangaroo grass Themeda triandra - Mitchell grass, barley Astrebla pectinata Mitchell grass, bull Astrebla squarrosa Mitchell grass, hoop Astrebla elymoides Plume sorghum Sorghum plumosum + Sabi grass Urochloa mosambicensis - Silky browntop Eulalia aurea (E. julva) - +" Wild rice Oryza australiensis Intermediate value grasses (perennials and annuals) Barbwire grass Cymbopogon rejractus Bottle washer or limestone grass Enneapogon polyphyllus + Early spring grass Eriochloa procera + Fire grass Schizachyrium spp. Flinders grass Iseilema spp. + Ribbon grass Chrysopogon jallax Liverseed Urochloa panico ides + Love grasses Eragrostis species + Pitted bluegrass Bothriochloa decipiens Annual sorghum Sorghum timorense Red natal grass Melinis repens (Rhynchelytrum) + Rice grass Xerochloa imburbis Salt water couch Sporobolus virginicus Spinifex, soft Triodia pungens Spinifex, curly Triodia bitextusa (Plectrachne pungens) Spiny mud grass Pseudoraphis spinescens White grass Sehima nervosum Wanderrie grass Eriachne spp. Native millet Panicum decompositum + Annual and less desirable grasses Asbestos grass Pennisetum basedowii Button grass Dacty loctenium -
Mimosa Diplotricha Giant Sensitive Plant
Invasive Pest Fact Sheet Asia - Pacific Forest Invasive Species Network A P F I S N Mimosa diplotricha Giant sensitive plant The Asia-Pacific Forest Invasive Species Network (APFISN) has been established as a response to the immense costs and dangers posed by invasive species to the sustainable management of forests in the Asia-Pacific region. APFISN is a cooperative alliance of the 33 member countries in the Asia-Pacific Forestry Commission (APFC) - a statutory body of the Food and Agricultural Organization of the United Nations (FAO). The network focuses on inter-country cooperation that helps to detect, prevent, monitor, eradicate and/or control forest invasive species in the Asia-Pacific region. Specific objectives of the network are: 1) raise awareness of invasive species throughout the Asia-Pacific region; 2) define and develop organizational structures; 3) build capacity within member countries and 4) develop and share databases and information. Distribution: South and Scientific name: Mimosa diplotricha C.Wright South-East Asia, the Pacific Synonym: Mimosa invisa Islands, northern Australia, South and Central America, the Common name: Giant sensitive plant, creeping Hawaiian Islands, parts of sensitive plant, nila grass. Africa, Nigeria and France. In India, it currently occurs Local name: Anathottawadi, padaincha (Kerala, throughout Kerala state and in India), banla saet (Cambodia), certain parts of the northeast, duri semalu (Malaysia), makahiyang lalaki especially the state of Assam. Its Flowers (Philippines), maiyaraap thao (Thailand), occurrence in other states is Cogadrogadro (Fiji). unknown and needs to be ascertained. M. diplotricha has Taxonomic position: not attained weed status in the Mimosa stem with prickles Division: Magnoliophyta Americas, Western Asia, East Class: Magnoliopsida, Order: Fabales Africa and Europe. -
Mimosa (Albizia Julibrissin)
W232 Mimosa (Albizia julibrissin) Becky Koepke-Hill, Extension Assistant, Plant Sciences Greg Armel, Assistant Professor, Extension Weed Specialist for Invasive Weeds, Plant Sciences Origin: Mimosa is native to Asia, from Iran to Japan. It was introduced to the United States in 1745 as an ornamental plant. Description: Mimosa is a legume with double-compound leaves that give the 20- to 40-foot tree a fern-like appear- ance. Each leaf has 10 to 25 leaflets and 40 to 60 subleaflets per leaflet. In the summer, the tree pro- duces pink puff flowers. Fruits are produced in the fall and are contained in tan seedpods. The tree often has multiple stems and a broad, spreading canopy. Seed- lings can be confused with other double-compound legumes, but mimosa does not have thorns or prickles like black locust (Robinia pseudoacacia), and has a woody base, unlike hemp sesbania (Sesbania exaltata). Habitat: Mimosa is cold-hardy to USDA hardiness zone 6 and is not found in elevations above 3,000 feet. Mimosa will thrive in full sun in a wide range of soils in any dis- turbed habitat, such as stream banks, roadsides and old fields. Mimosa can live in partial shade, but is almost never found in full shade or dense forests. Mi- mosa often spreads by seeds from nearby ornamental plantings, or by fill dirt containing mimosa seeds. It is a growing problem in aquatic environments, where mimosa gets started on the disturbed stream banks, and its seeds are carried by the running water. Environmental Impact: Mimosa is challenging to remove once it is estab- lished. -
The Degradation of the Asphalt Alleys by Rhizomes of Herbaceous Plant Species of Couch Grass
Recent Advances in Energy, Environment and Geology The Degradation of the Asphalt Alleys by Rhizomes of Herbaceous Plant Species of Couch Grass FILIPOV Feodor*1, ROBU Teodor**2 1* Soil sciences Department, Faculty of Agriculture 3, Ion Ionescu de la Brad" University of Agricultural Sciences and Veterinary Medicine of Iasi, Mihail Sadoveanu Alley, 700490, Iasi, Romania, +40232407450, [email protected] **2Crop science department, Ion Ionescu de la Brad" University of Agricultural Sciences and Veterinary Medicine of Iasi, Mihail Sadoveanu Alley, 700490, Iasi, Romania, +40232407450, teorobu@uaiasi Abstract: - The soil cover of urban areas consists of several soil taxonomic units with significantly altered properties and functions. Soils covered by asphalt or another compact materials (such as concrete materials), also known under the name of or ekranic Technosols [1, 2], have strongly modified properties and perform only part of the specific functions that allow only low biological activity and root growth of some plants species. Soil under asphalted alleys have water retention capacity and allows expansion of the roots of woody plants and grasses. The soil horizons under asphalt pavers can be developed only a small number of plant species that are tolerant of deficient aeration. It is well known that the concentration of oxygen decrease considerable and the concentration of carbon dioxide increase significantly (>10% or even 20%) in the compacted soil layers or in the soil layers under asphalt [3, 4]. Some physical soil properties of such as bulk density, compaction degree, air porosity, total soil porosity are substantially modified. Frequentlly, the values of physical properties of soils covered with asphalt indicate that soils are a strong compacted. -
Download Sanders-2019-Plantspeopleplanet.Pdf
DOI: 10.1002/ppp3.6 EDITORIAL Trapped in time: Lingering with “Plantness” 1 | INTRODUCTION 2 or 3 times, & then at same rate untwists & twists in opposite direction. It generally rests half an hour before In modern urban existence, the complex lives of plants are often re‐ it retrogrades. The stem does not become permanently duced to simplistic categories, which resonate with human utility; twisted. The stem beneath the twisting portion does not as Jahren (2016) noted: “Human civilization has reduced the plant, move in the least, though not tied. The movement goes a four‐hundred‐million‐year‐old life form, into three things: food, on all day & all early night— It has no relation to light for medicine and wood” (p. 279). These categories speak little of the the plant stands in my window & twists from the light just contributions plants make to the ecological fabric of life on Earth; as quickly as towards it. both on land and in the oceans, nor to the exploitation of humans (Darwin Correspondence Project Letter) by plants, for example, Darnel Lolium temulentum (Thomas, Archer, & Marggraf Turley, 2016); neither do they acknowledge the complex Unlike Charles Darwin, contemporary urban humans “are largely inter‐ and intrasystems in which plants live out their lives (Gagliano, asynchronous with plants” and “have neither the patience nor the 2015; Iverson et al., 2017). The temporal zones that plants inhabit capacity to linger with them, to accompany their development and need to be multifaceted: the “capability to sense and respond to ex‐ growth” (Marder, 2013, p. 19). But what if city dwellers did stay and lin‐ ternal mechanical stimuli at various timescales is essential to many ger with their houseplants? What might they witness? (Sanders, 2018) physiological aspects in plants, including self‐protection, intake of (Figures 1 and 2). -
Alien Plants in Central European River Ports
A peer-reviewed open-access journal NeoBiota 45: 93–115 (2019) Alien plants in Central European river ports 93 doi: 10.3897/neobiota.45.33866 RESEARCH ARTICLE NeoBiota http://neobiota.pensoft.net Advancing research on alien species and biological invasions Alien plants in Central European river ports Vladimír Jehlík1, Jiří Dostálek2, Tomáš Frantík3 1 V Lesíčku 1, 150 00 Praha 5 – Smíchov, Czech Republic 2 Silva Tarouca Research Institute for Landscape and Ornamental Gardening, CZ-252 43 Průhonice, Czech Republic 3 Institute of Botany, Academy of Sciences of the Czech Republic, CZ-252 43 Průhonice, Czech Republic Corresponding author: Jiří Dostálek ([email protected]) Academic editor: Ingo Kowarik | Received 14 February 2019 | Accepted 27 March 2019 | Published 7 May 2019 Citation: Jehlík V, Dostálek J, Frantík T (2019) Alien plants in Central European river ports. NeoBiota 45: 93–115. https://doi.org/10.3897/neobiota.45.33866 Abstract River ports represent a special type of urbanized area. They are considered to be an important driver of biological invasion and biotic homogenization on a global scale, but it remains unclear how and to what degree they serve as a pool of alien species. Data for 54 river ports (16 German, 20 Czech, 7 Hungarian, 3 Slovak, and 8 Austrian ports) on two important Central European waterways (the Elbe-Vltava and Dan- ube waterways) were collected over 40 years. In total, 1056 plant species were found. Of these, 433 were alien, representing 41% of the total number of species found in all the studied Elbe, Vltava, and Danube ports. During comparison of floristic data from literary sources significant differences in the percentage of alien species in ports (50%) and cities (38%) were found.