Weed Descriptions

Total Page:16

File Type:pdf, Size:1020Kb

Weed Descriptions Weed Descriptions Part II Perennial sowthistle Sonchus arvensis Life Cycle perennial, reproducing by seed and creeping roots; found in cultivated fields, pastures, and waste areas. Cotyledons are ovate with a small indentation at the tip; somewhat fleshy with milky juice. Leaves are 4 to 8 inches long, alternate, lobed, and have spiny edges. Stems are smooth, 3 to 7 feet tall, and have a milky juice. Flowers are borne in heads about 1 1/2 inches across; yellow. Horsenettle Solanum carolinense Life Cycle perennial, spreading by seeds and creeping rootstocks; found in fields, gardens, and waste areas, especially those with sandy soil. Cotyledons are lanceolate; smooth with hairs on margins. Leaves are alternate; with dense hairs; dark green on upper surface; later leaf midribs and petioles with spines; margins undulate to sparsely toothed; petioles are short and hairy. Stems are green to purple; erect; dense hairs; usually crooked at nodes; prickly. Horseweed (Marestail) Conyza canadensis Life Cycle annual, reproducing by seed; found in pastures, roadsides, and wasteland. Cotyledons are ovate and hairless. Leaves alternate at first; entire, mostly smooth; later leaves becoming hairy; serrated margins; lanceolate; petioles are short to moderate in length; clasping; hairy on upper surface. Stems are stout; erect; 1 to 6 feet tall; unbranched at base. Ivyleaf morningglory Ipomoea hederacea Life Cycle annual, reproducing by seed; found in gardens, fields, and waste places; common in corn and soybean fields. Cotyledons are butterfly-shaped, shiny, and deeply notched at the tip; the stem below the cotyledons is dull purple with a ridge running from the base of each cotyledon. Leaves are alternate; hairy; 3-lobed and ivy- shaped; petioles are long; hairy with reddish tint. Stems are hairy; twining and climbing or trailing on the ground. Jimsonweed Datura stramonium Life Cycle annual, reproducing by seed; found in cultivated crops on fertile soil and especially in old feedlots. Cotyledons are smooth and lance-shaped; prominent midrib; the stem below the cotyledon is often purplish. Leaves are alternate; large; smooth; ovate with irregularly toothed edges; distinctive rank odor when crushed; petioles are long, pale green to purple, and may have short hairs. Stems are smooth; thick; branching widely on upper part. Johnsongrass Sorghum halepense Life Cycle perennial grass, reproducing by seed and large rhizomes; found especially on rich soil; common in corn and soybeans in bottomlands. Seedling leaves are hairless; seedlings resemble young corn or grain sorghum. Leaves are simple; smooth; alternate; 6 to 20 inches long; 1/2 to 1 1/2 inches wide; stems are erect; stout; 1 1/2 to 6 feet tall; leaf sheath hairless; no auricles; prominent, jagged, membranous ligule. Flowers are borne in panicles that are large, purplish, and hairy. Ladysthumb smartweed Polygonum persicaria Life Cycle annual, reproducing by seed; found in cultivated fields, waste places, and along ditches. Cotyledons are lance-shaped with rounded tips and smooth on both surfaces. Leaves are narrow; pointed; have smooth margins; usually with dark spot in the middle of the leaf; short petioles. Stems are smooth; branched; sometimes hairy; clear membrane at leaf nodes. Flowers are pink or purplish in dense erect, terminal and axillary spikes. Large crabgrass Digitaria sanguinalis Life Cycle annual grass, reproducing by seed; found in lawns, gardens, and fields. Seedling leaves—the first leaf is short and wide with a blunt tip. Ligule is membranous; no auricles; medium; jagged margins; sheaths are densely hairy. Leaves are hairy; margins often wrinkled. Stems often root at lower nodes. Musk thistle Carduus nutans Life Cycle biennial, reproducing by seed; found in pastures, meadows, and waste areas. Cotyledons are lance-shaped, dull green, and have broad white veins. Leaves smooth; light colored; very spiny margins; after stem elongation, leaf margins extend down stem. Stems do not elongate in first year; thereafter, erect and spiny with spiny wings; 3 to 6 feet tall; lower portion branched. Peppergrass Lepidium virginicum Life Cycle annual or winter annual, reproducing by seed; found in winter wheat, first-year pastures, and waste places. Cotyledons lack hairs, have a peppery taste, and are unequally oval, with long petioles. Leaves lanceolate to linear; coarsely toothed; usually lacking petioles. Stems branched; 6 to 18 inches high; hairless or with fine hairs. Flowers small, white, four-petaled; borne on racemes that bloom constantly, so they may show flowers on top and seed pods below. Pigweeds (Redroot, Smooth) Amaranthus species Life Cycle annual, reproducing by seed; found in cultivated fields, fence rows, and waste places. Cotyledons are linear and hairless. Leaves are alternate; ovate to oval, usually with a notched tip; prominently veined; leaf tissue between veins appearing puffy and rough; younger leaves pink-tinged on bottom surface; purplish midvein; petioles are green to pink-tinged, long, and grooved on upper surface with appressed hairs. Stems are rough; hairy; vertically ridged; branching widely if not crowded; pinkish, turning red below soil surface. Prickly lettuce Lactuca serriola Life Cycle annual, sometimes a biennial; found in roadsides, fencerows, and wasteland. Cotyledons are oval to spatula-shaped; the upper surface and margins are hairy. Leaves are large, coarse, all with prickles along the margins and along the lower midribs; contain milky juice. Flowers appear in large, terminal, pyramid- shaped clusters. Stems are erect; 2 to 6 feet tall; stiff; hollow. Root is a large taproot. Prickly sida Sida spinosa Life Cycle annual, reproducing by seed; found late in the season in waste places, cultivated fields, gardens, and pastures. Cotyledons are rounded to heart-shaped, have hairy margins, and have a shallow indentation or notch at the apex; the stem below cotyledons is covered with short, velvety hairs. Leaves are alternate; oblong; sparsely hairy; saw-toothed margins; yellow-green; petioles are long and covered with short, gland-tipped hairs. Stems are branching widely; softly hairy; bearing 2 to 3 short, blunt spiny projections below each node. Prostrate knotweed Polygonum aviculare Life Cycle annual, reproducing by seeds; found in trampled areas in lawns, waste places, and along roadways or paths. Cotyledons are united at the base to form a small cup. Leaves are bluish-green, alternate, oblong, narrowed at the base and pointed at the tip. Stems are bluish-green; leafy; wiry; extending 4 to 24 inches in all directions from the taproot, forming a mat; nodes are covered with thin papery sheaths. Purslane Portulaca oleracea Life Cycle annual, reproducing by seed; found in fields and waste places. Cotyledons are succulent, linear, and hairless; tinged with bright red; the stem below cotyledons is bright red and succulent. Leaves are oblanceolate; fleshy; maroon on edges; opposite; smooth; petioles are short, fleshy, and flattened on upper surface. Stems are juicy; smooth; often reddish; prostrate and ascending toward ends. Flowers are small, star-shaped, and yellow; borne in axillary clusters. Quackgrass Elymus repens Life Cycle perennial grass, spreading by seeds and rhizomes; found in waste places, pastures, and cultivated areas. Seedling leaves are slightly hairy and bright green; the lower part of the stem is often pinkish brown and hairy. Ligule is membranous and short; sheaths have lower parts with short hairs; upper parts smooth. Leaves are rough above; sparsely hairy to smooth below; constriction often showing near tip; auricles present—a slender, clawlike structure at the base of the blade and clasping the stem. Rhizomes are long; slender; sharp; white. Shattercane Sorghum bicolor Life Cycle annual grass, reproducing by seed; found in cultivated fields where it reseeds itself. Ligule is long; membranous; apical margin jagged with short hairs; sheaths are smooth to rough with membranous margins. Leaves are finely veined; smooth to sparsely hairy; vigorous growth; bigger than most annuals. Roots are fibrous. Shepherd’s-purse Capsella bursa-pastoris Life Cycle annual, reproducing by seeds; found in cultivated and noncultivated areas. Cotyledons and early leaves are oval to spatula-shaped with long petioles; cotyledons have a grainy appearance; the stem below cotyledons is dull green with some purplish tones. Leaves in a rosette are coarsely serrate and 2 to 4 inches long. Stems are erect, 1 to 1 1/2 feet tall. Flowers are small, white, 4-petaled; fruit is a triangular pod that contains about 20 seeds. Stinkgrass Eragrostis cilianensis Life Cycle annual grass; found in cultivated fields and waste places. Leaves have smooth sheaths except for hairs on upper portion; flat, smooth blades. Stems are slender, smooth, and 1 to 2 feet tall, branched at the top; several stems arise from the crown; plant has a disagreeable odor. Flowers are in branched panicles; spikelets are flat, containing 20 to 40 florets. Tall morningglory Ipomoea purpurea Life Cycle annual, reproducing by seeds; found in gardens, fields, and waste places. Cotyledons are shiny; smooth; oval with deeply indented tip and base to give a butterfly or kidney shape. Leaves are alternate; hairy; broadly heart- shaped with pointed tip; petioles are long, hairy, and dull green to reddish in color. Stems are hairy; twining or trailing on the ground. Flowers are blue, purple, white, or variegated. Velvetleaf Abutilon theophrasti Life Cycle annual, reproducing by seed; found
Recommended publications
  • Genetic Suppression of Plant Development and Chloroplast Biogenesis Via the Snowy Cotyledon 3 and Phytochrome B Pathways
    CSIRO PUBLISHING Functional Plant Biology, 2015, 42, 676–686 http://dx.doi.org/10.1071/FP15026 Genetic suppression of plant development and chloroplast biogenesis via the Snowy Cotyledon 3 and Phytochrome B pathways Diep Ganguly A, Peter Crisp A, Klaus Harter B, Barry J. Pogson A and Verónica Albrecht-Borth A,C AARC (Australian Research Council) Centre of Excellence in Plant Energy Biology, Research School of Biology, Australian National University Canberra, Acton, ACT 0200, Australia. BZentrum für Molekularbiologie der Pflanzen, Plant Physiology, University of Tübingen, 72076 Tübingen, Germany. CCorresponding author. Email: [email protected] Abstract. Plant development is regulated by external and internal factors such as light and chloroplast development. A revertant of the Arabidopsis thaliana (L.) Heyhn. chloroplast biogenesis mutant snowy cotyledon 3 (sco3–1) was isolated partially recovering the impaired chloroplast phenotype. The mutation was identified in the Phytochrome B (PhyB) gene and is a result of an amino acid change within the PAS repeat domain required for light-induced nuclear localisation. An independent phyB-9 mutation was crossed into sco3–1 mutants, resulting in the same partial reversion of sco3–1. Further analysis demonstrated that SCO3 and PhyB influence the greening process of seedlings and rosette leaves, embryogenesis, rosette formation and flowering. Interestingly, the functions of these proteins are interwoven in various ways, suggesting a complex genetic interaction. Whole-transcriptome profiling of sco3–1phyB-9 indicated that a completely distinct set of genes was differentially regulated in the double mutant compared with the single sco3–1 or phyB-9 mutants. Thus, we hypothesise that PhyB and SCO3 genetically suppress each other in plant and chloroplast development.
    [Show full text]
  • BIO 102 General Biology Lecture Outline Plantae I. Introduction A. Taxonomy Domain
    BIO 102 General Biology Lecture Outline Plantae I. Introduction A. Taxonomy Domain: Eukarya Kingdom: Plantae B. General characteristics Multicellular Autotrophic / Photosynthetic Cellulose cell wall Reproduction – alternation of generations C. Life cycle Alternation of generations Haploid = gametophyte, which produces gametes via mitosis Diploid = sporophyte, which produces spores via meiosis Meiosis = cell division from 2n to n Mitosis = cell division either from 2n to 2n, OR from n to n Fertilization = combine gametes: n + n = 2n Homospory vs. heterospory II. Major Groups of Plants A. Characterized by 4 criteria in branching manner Vascular vs. non-vascular Seed production or lack thereof Types of seeds produced Development & morphology B. Non-tracheophytes (nonvascular plants) General characteristics No vascular tissue Gametophyte (haploid) generation dominant Requires water for reproduction Examples Liverworts Hornworts Mosses Moss reproductive cycle C. Tracheophytes General characteristics Vascular tissue: Xylem and Phloem Specialized tissues: Leaves Roots Stems Cuticles Stomata Sporophyte (diploid) generation dominant Divisions based on seed-bearing vs. non-seed bearing (Seed vs. spore) D. Seedless plants BIO 102 General Biology Lecture Outline General characteristics Have vascular tissue but lack seeds Examples Ferns Whisk ferns Club mosses Horsetails E. Seed-bearing plants General characteristics Have vascular tissue and seeds Divisions based on whether seeds are “covered” or not F. Gymnosperms General characteristics Vascular plants with “naked” seeds = i.e., no fruit Examples Conifers Gingkos Cycads Gnetophytes Gymnosperm life cycle G. Angiosperms General characteristics Vascular plants with “covered” seeds = i.e., seeds within fruits Fruits are derived from flowers Angiosperm = flowering plant Divisions are based on development and plant morphology (i.e., structures) Angiosperm life cycle H.
    [Show full text]
  • Eudicots Monocots Stems Embryos Roots Leaf Venation Pollen Flowers
    Monocots Eudicots Embryos One cotyledon Two cotyledons Leaf venation Veins Veins usually parallel usually netlike Stems Vascular tissue Vascular tissue scattered usually arranged in ring Roots Root system usually Taproot (main root) fibrous (no main root) usually present Pollen Pollen grain with Pollen grain with one opening three openings Flowers Floral organs usually Floral organs usually in in multiples of three multiples of four or five © 2014 Pearson Education, Inc. 1 Reproductive shoot (flower) Apical bud Node Internode Apical bud Shoot Vegetative shoot system Blade Leaf Petiole Axillary bud Stem Taproot Lateral Root (branch) system roots © 2014 Pearson Education, Inc. 2 © 2014 Pearson Education, Inc. 3 Storage roots Pneumatophores “Strangling” aerial roots © 2014 Pearson Education, Inc. 4 Stolon Rhizome Root Rhizomes Stolons Tubers © 2014 Pearson Education, Inc. 5 Spines Tendrils Storage leaves Stem Reproductive leaves Storage leaves © 2014 Pearson Education, Inc. 6 Dermal tissue Ground tissue Vascular tissue © 2014 Pearson Education, Inc. 7 Parenchyma cells with chloroplasts (in Elodea leaf) 60 µm (LM) © 2014 Pearson Education, Inc. 8 Collenchyma cells (in Helianthus stem) (LM) 5 µm © 2014 Pearson Education, Inc. 9 5 µm Sclereid cells (in pear) (LM) 25 µm Cell wall Fiber cells (cross section from ash tree) (LM) © 2014 Pearson Education, Inc. 10 Vessel Tracheids 100 µm Pits Tracheids and vessels (colorized SEM) Perforation plate Vessel element Vessel elements, with perforated end walls Tracheids © 2014 Pearson Education, Inc. 11 Sieve-tube elements: 3 µm longitudinal view (LM) Sieve plate Sieve-tube element (left) and companion cell: Companion cross section (TEM) cells Sieve-tube elements Plasmodesma Sieve plate 30 µm Nucleus of companion cell 15 µm Sieve-tube elements: longitudinal view Sieve plate with pores (LM) © 2014 Pearson Education, Inc.
    [Show full text]
  • Early Soybean Growth and Development
    EARLY SOYBEAN GROWTH AND DEVELOPMENT A soybean seed has two distinct parts: the cotyledons and the embryo. The two cotyledons are the main food storage structure, which supply food during emergence and for the seven to ten days after emergence through the V1 growth stage. The embryo itself is comprised of three parts. 1. The radicle is the first root and it’s the first part of the embryo to penetrate the seed coat. Lateral roots form from the radicle, and tiny root hairs then develop on the lateral roots. Root hairs are the main absorbing surface of the entire root system. A soybean’s root system branches and rebranches within the first four to five weeks after planting, with the bulk of root mass persisting in the top six inches of soil. 2. The hypocotyl is the stem below the cotyledon. It begins to elongate after the radicle and forms an arch, which is pushed upward. As the arch breaks the soil surface, it pulls the cotyledons and epicotyl up. The uppermost cells of the hypocotyl stop growing as cells on the underside continue to straighten the arch. This process lifts the cotyledons into an upright position. 3. The epicotyl is comprised of the small leaves, stem and the apical growing point. The epicotyl is protected between the cotyledons until after emergence. The loss of a cotyledon is not lethal to the seedling, but damage to the epicotyl is. The hypocotyl arch is a large structure that is relative to seed size, utilizing considerable seed energy to push through the soil.
    [Show full text]
  • Red Cotyledon of Lettuce Study of Abnormality Shows Seedling Growth Not Always Retarded, Calls for Modified Germination Requirements
    Red Cotyledon of lettuce study of abnormality shows seedling growth not always retarded, calls for modified germination requirements Wesley H. Dempsey and James F. Harrington Many lettuce seedlings with red coty- must have produced normal plants. Evi- ledons--seed leaves-produce normal dently a slight reddening of the cotyledon plants, and their general classification as is not serious enough to produce a weak abnormal is not justified. plant as long as the roots are normal. The high percentage of seedlings with To further test the effect of red coty- red cotyledons constitutes a new problem ledon on subsequent plant growth, trans- for California lettuce seed growers and plants were made from the germination seedsmen. Because of the inflexible rules tests of normal, abnormal C, and abnor- defining a normal seedling, seed analysts mal B seedlings. There were three repli- are forced to call reddening of the coty- cations of each lot. After four weeks ledons symptoms of abnormality. As a growth in flats in\the greenhouse all result, many lots are rated low in germi- plants appeared to be growing normally. nation even though most of the seedlings Fresh weight determinations were made are normal except for the reddening of of each treatment. The results are shown Red cotyledon condition in lettuce seedlings. the cotyledons. N is a normal seedling; c, b, and a are three in the following table. A slight but sig- An investigation was undertaken to de- categories of abnormal seedlings. nificant retardation of growth had oc- termine the effect of the red cotyledon curred among the B seedlings.
    [Show full text]
  • AGR-223: Identifying Soybean Growth Stages
    AGR-223 University of Kentucky College of Agriculture, Food and Environment Identifying Soybean Growth Stages Cooperative Extension Service Carrie A. Knott and Chad Lee, Plant and Soil Sciences ccurate identification of soybean Soybean growth stages are divided a soybean field that has 10 percent of the growth stages is important to maxi- into two phases: vegetative (V) and re- plants with two fully developed trifoliate mizeA grain yield and profitability, because productive (R) (Table 1). When identify- leaves (V2), 60 percent of the plants with most management decisions are based ing vegetative growth stages of soybean three fully developed trifoliate leaves upon the growth stage of soybean plants (figures 1 to 5), the primary consideration (V3), and 30 percent of the plants with within the fields. Two plant growth habits is the number of fully developed leaves four fully developed trifoliate leaves exist for soybean: indeterminate and on the main stem. A fully developed leaf (V4) will be the V3 growth stage. This is determinate. Indeterminate cultivars can is one that has all leaflets open (Figure because 70 percent of the field is or has produce both vegetative and reproduc- 4), while an undeveloped leaf has leaflet already been the V3 growth stage. tive growth simultaneously until about edges that are still touching (figures 2 and Key features of soybean growth stages R5 growth stage. Most indeterminate 3). Reproductive growth stages (figures 6 are highlighted within this guide. For a cultivars are maturity groups 00 to IV. to 13) are identified by specific flower, comprehensive description of soybean In contrast, determinate cultivars will pod, and seed characteristics.
    [Show full text]
  • Plant ID. Agricultural Lesson Plans. INSTITUTION Southern Illinois Univ., Carbondale
    DOCUMENT RESUME ED 364 744 CE 065 309 TITLE Plant ID. Agricultural Lesson Plans. INSTITUTION Southern Illinois Univ., Carbondale. Dept. of Agricu ral Education and Mechanization. PUB DATE 92 NOTE 33p.; For related documents, see CE 065 306-311. PUB TYPE Guides Classroom Use Teaching Guides (For Teacher) (052) EDRS PRICE MF01/PCO2 Plus Postage. DESCRIPTORS *Agricultural Education; Behavioral Objectives; *Classification; Learning Activities; Lesson Plans; *Plant Growth; *Plant Identification; *Plants (Botany); Secondary Education ABSTRACT This lesson plan is intended for use in conducting classes on plant identification. Presented first are a series of questions and answers designed to convey general information about the scientific classification of plants. The following topicsare among those discussed: main types of plants; categories of vascular plants; gymnosperms and angiosperms; dicots; monocots; plant families; and classification of plants by their parts (leaves, stems, flowers, seeds, and roots), life cycle, and/or hardiness. Also provided are the following: a glossary of pertinent scientific terms, four worksheets, answers to the worksheets, a quiz and quizanswers, six overhead transparency masters, and a lesson plan for teaching students to identify 10 plants. Included in the lesson planare an objective, list of equipment needed, detailed steps for completing the activity, and student activity record sheet. (MN) *********************************************************************** Reproductions supplied by EDRS are the best
    [Show full text]
  • Swahili-English Dictionary, the First New Lexical Work for English Speakers
    S W AHILI-E N GLISH DICTIONARY Charles W. Rechenbach Assisted by Angelica Wanjinu Gesuga Leslie R. Leinone Harold M. Onyango Josiah Florence G. Kuipers Bureau of Special Research in Modern Languages The Catholic University of Americ a Prei Washington. B. C. 20017 1967 INTRODUCTION The compilers of this Swahili-English dictionary, the first new lexical work for English speakers in many years, hope that they are offering to students and translators a more reliable and certainly a more up-to-date working tool than any previously available. They trust that it will prove to be of value to libraries, researchers, scholars, and governmental and commercial agencies alike, whose in- terests and concerns will benefit from a better understanding and closer communication with peoples of Africa. The Swahili language (Kisuiahili) is a Bantu language spoken by perhaps as many as forty mil- lion people throughout a large part of East and Central Africa. It is, however, a native or 'first' lan- guage only in a nnitp restricted area consisting of the islands of Zanzibar and Pemba and the oppo- site coast, roughly from Dar es Salaam to Mombasa, Outside this relatively small territory, elsewhere in Kenya, in Tanzania (formerly Tanganyika), Copyright © 1968 and to a lesser degree in Uganda, in the Republic of the Congo, and in other fringe regions hard to delimit, Swahili is a lingua franca of long standing, a 'second' (or 'third' or 'fourth') language enjoy- ing a reasonably well accepted status as a supra-tribal or supra-regional medium of communication. THE CATHOLIC UNIVERSITY OF AMERICA PRESS, INC.
    [Show full text]
  • Seedling Emergence Patterns
    1 Seedling emergence patterns Learning objective: To be able to recognize the two major seedling emergence patterns. Background information: There are two common patterns of seedling emergence. The most common pattern is where the cotyledons are raised above ground as the seedling emerges. The seedling forms a hypocotyl hook that pushes through the soil. Once the seedling reaches the light, the hook opens to create a straight seedling. This pattern is called epigeous. In the second pattern, the cotyledons remain underground and the stem (epicotyl) emerges above ground. This pattern is called hypogeous. Large seeded plants like Kentucky coffeetree and oaks tend to have hypogeous germination. The cotyledons function as the repository for food reserves in the seed. During seed development the plant stores food in the cotyledons that the seedling will use for emergence. Once the seedling emerges into the sunlight, it can begin to make its own food through photosynthesis. 2 In the group of plants covered in this website, the oaks, nuts (Ohio buckeye, black walnut and pecan), paw paw, and Kentucky coffeetree have a hypogeous seedling emergence pattern. For black walnut, pecan, and paw paw, the cotyledons never emerge from the seed. All the other plant species on the website have a epigeous seedling emergence pattern. An easy comparison can be made using Kentucky coffeetree and honeylocust. They are both in the legume family and only have physical dormancy. The seeds are easy to collect, are large and store for a very long time so the experiment can be conducted any time of the year. Procedures: 1.
    [Show full text]
  • Cotyledon Orbiculata
    Alfred Maroyi /J. Pharm. Sci. & Res. Vol. 11(10), 2019, 3491-3496 A review of botany, medicinal uses, phytochemistry and biological activities of Cotyledon orbiculata Alfred Maroyi Department of Biodiversity, University of Limpopo, Private Bag X1106, Sovenga 0727, South Africa. Abstract Cotyledon orbiculata is a succulent shrub widely used as herbal medicine throughout its distributional range in southern Africa. This study is aimed at providing a critical review of the botany, biological activities, phytochemistry and medicinal uses of C. orbiculata. Documented information on the botany, biological activities, medicinal uses and phytochemistry of C. orbiculata was collected from several online sources which included BMC, Scopus, SciFinder, Google Scholar, Science Direct, Elsevier, Pubmed and Web of Science. Additional information on the botany, biological activities, phytochemistry and medicinal uses of C. orbiculata was obtained from pre-electronic sources such as book chapters, books, journal articles and scientific publications sourced from the University library. This study showed that the leaves, leaf sap and roots of C. orbiculata are mainly used as herbal medicines for earache, epilepsy, infertility, respiratory problems, sexually transmitted infections, skin problems, sores and wounds, toothache, ulcers and worms. Phytochemical compounds identified from C. orbiculata include cardiac glycosides, flavonoids, gallotannin, phenols, reducing sugar, saponins, tannins and triterpene steroids. Pharmacological research revealed that C.
    [Show full text]
  • Weed Seedling Identification Guide This Guide Is Not a Complete List of All the Weeds to Be Found in Croplands Or Rangelands
    EB0215 Weed Seedling for Montana and the Northern Identification Guide Great Plains by Hilary Parkinson, Jane Mangold and Fabian Menalled This project was funded in part by the Montana Department of Agriculture’s Noxious Weed Trust Fund; Montana Wheat and Barley Commission; Extension Integrated Pest Management (EIPM) through the USDA; and USDA National Institute of Food and Agriculture through the Western Integrated Pest Management Center. We would like to thank Susan Anderegg for her work designing and assembling this publication; Matt Lavin, Rose Malisani, Bobbie Roos and Steve Young for their reviews; and Bugwood.org for sharing their large collection of high quality photos. Hilary Parkinson Plant Identification Diagnostician and Research Associate Jane Mangold Assistant Professor, Extension Invasive Plant Specialist Fabian Manalled Associate Professor, Extension Cropland Weed Specialist © 2013 Montana State University Extension EB0215 The U.S. Department of Agriculture (USDA), Montana State University and Montana State University Extension prohibit discrimination in all of their programs and activities on the basis of race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, and marital and family status. Issued in furtherance of cooperative extension work in agriculture and home economics, acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, Jill Martz, Director of Extension, Montana State University, Bozeman, MT 59717. i TABLE OF CONTENTS Weed seedling identification: A keystone component of integrated weed Weed Seedling Identification management (IWM). Principles of IWM . iii Tips on using this guide . vi Rapid and accurate identification of weeds at the seedling stage is the first step in the design of a successful weed management program that saves Broadleaf Weeds producers and land managers time and money, and reduces herbicide use.
    [Show full text]
  • Anatomy and Morphology of the Cotton Seed and Seedling
    Chapter 1 ANATOMY AND MORPHOLOGY OF THE COTTON SEED AND SEEDLING Jack Mauney, Jarman Enterprises, Mesa, Arizona 85201 INTRODUCTION The structures of the seed of the cotton plant (Gossypium sp.) have been described in great detail by Brown (1927), Baranov and Maltzev (1937), Leahy (1948), Tharp (1965), Mauney (1968), and 0osterhuis and Jerstadt (1999). The definitive structures of the seed and seedling which influence the development of the subsequent crop are: 1) vascular connections, 2) seed coat and chalazal pore connections, 3) cotyledons, 4) hypocotyl and radicle axis, and 5) apex. This review will concentrate upon these five elements of the seed anatomy and morphology. VASCULAR CONNECTIONS OF THE SEED During development the seed is connected to the vascular system of the plant through the attachment of the funiculus to the placenta of the boll (Figure 1K). There are vascular strands consisting primarily of phloem in the raphe (Fig 1, J) of the seed extending to the chalazal pore on the distal portion of the developing seed. The vascular strands end at the pore. Thus, all hy- dration and nutrition for the developing embryo must enter the embryo sac through the spongy (unvascularized) tissue of the chalazal pore. This arrangement enables the plant to bathe the developing embryo in endosperm with very high osmotic potential (Mauney, 1961; Trolinger, et al., 1993) while the canopy operates at familiar, and fluctuating, water potential (Van Iersel et al., 1994, Van Iersel et al., 1995; Van Iersel and Oosterhuis, 1996) SEED COAT AND CHALAZAL PORE STRUCTURE Seed dormancy is evolutionarily and culturally necessary for cotton which has a long period of exposure to weather before harvest.
    [Show full text]