Sea-Beach Amaranth Amaranthus Pumilus Rafinesque
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Amaranthus Pumilus (Seabeach Amaranth)
Bartonia No. 61, 2002-News and Notes Amaranthus pumilus Raf. (Seabeach Amaranth, Amaranthaceae) Rediscovered in Sussex County, Delaware In August of 2000, Amaranthus pumilus was rediscovered in Sussex Co., Delaware after 125 years without a sighting. It was first collected in Delaware in 1875 by Albert Commons (10 September 1875, A. Commons, s.n., "seabeach, Baltimore Hundred, Delaware," PH). Amaranthus pumilus was federally listed as threatened by the U.S. Fish and Wildlife Service in 1993. Historically, this species was known from Massachusetts south to South Carolina (Weakley et al. 1996). Amaranthus pumilus was reported as rediscovered at Assateague Island National Seashore, Worcester County, Maryland in 1998 (Ramsey 2000). Prior to rediscovery on Assateague Island and in Sussex County, A. pumilus was extant on Long Island, New York, and in North Carolina and South Carolina. Lisa Marie Kendall of the Delaware Natural Heritage Program, Division of Fish and Wildlife, Delaware Department of Natural Resources discovered the first plants on 7 August 2000. Subsequent surveys revealed a total of 41 individuals scattered over 22 kilometers of Atlantic shoreline. All plants found are within the boundaries of Delaware Seashore and Fenwick Island State Parks. The largest number of plants (28) was found within a 1.5-km stretch of shoreline near the swimming beach at Delaware Seashore State Park. This section of beach is the only area where A. pumilus was found that is off-limits to vehicular traffic. This area provides the best habitat for the long-term survival of A. pumilus. Individual plants were found growing on relatively open sand near the base of the primary foredune. -
Weed Risk Assessment for Vitex Rotundifolia L. F. (Lamiaceae)
Weed Risk Assessment for Vitex United States rotundifolia L. f. (Lamiaceae) – Beach Department of Agriculture vitex Animal and Plant Health Inspection Service June 4, 2013 Version 2 Left: Infestation in South Carolina growing down to water line and with runners and fruit stripped by major winter storm (Randy Westbrooks, U.S. Geological Survey, Bugwood.org). Right: A runner with flowering shoots (Forest and Kim Starr, Starr Environmental, Bugwood.org). Agency Contact: Plant Epidemiology and Risk Analysis Laboratory Center for Plant Health Science and Technology Plant Protection and Quarantine Animal and Plant Health Inspection Service United States Department of Agriculture 1730 Varsity Drive, Suite 300 Raleigh, NC 27606 Weed Risk Assessment for Vitex rotundifolia Introduction Plant Protection and Quarantine (PPQ) regulates noxious weeds under the authority of the Plant Protection Act (7 U.S.C. § 7701-7786, 2000) and the Federal Seed Act (7 U.S.C. § 1581-1610, 1939). A noxious weed is defined as “any plant or plant product that can directly or indirectly injure or cause damage to crops (including nursery stock or plant products), livestock, poultry, or other interests of agriculture, irrigation, navigation, the natural resources of the United States, the public health, or the environment” (7 U.S.C. § 7701-7786, 2000). We use weed risk assessment (WRA)—specifically, the PPQ WRA model (Koop et al., 2012)—to evaluate the risk potential of plants, including those newly detected in the United States, those proposed for import, and those emerging as weeds elsewhere in the world. Because the PPQ WRA model is geographically and climatically neutral, it can be used to evaluate the baseline invasive/weed potential of any plant species for the entire United States or for any area within it. -
Vitex Rotundifolia L.F
NEW YORK NON -NATIVE PLANT INVASIVENESS RANKING FORM Scientific name: Vitex rotundifolia L.f. USDA Plants Code: VIRO80 Common names: Roundleaf chastetree, beach vitex, chasteberry, monk's pepper Native distribution: Asia (China, Japan), India, Sri Lanka, Mauritius, Australia, Pacific Islands (inlcuding Hawaii) Date assessed: 3 June 2009; edited August 19, 2009 Assessors: Steve Glenn, Gerry Moore Reviewers: LIISMA SRC Date Approved: August 19, 2009 Form version date: 3 March 2009 New York Invasiveness Rank: High (Relative Maximum Score 70.00-80.00) Distribution and Invasiveness Rank ( Obtain from PRISM invasiveness ranking form ) PRISM Status of this species in each PRISM: Current Distribution Invasiveness Rank 1 Adirondack Park Invasive Program Not Assessed Not Assessed 2 Capital/Mohawk Not Assessed Not Assessed 3 Catskill Regional Invasive Species Partnership Not Assessed Not Assessed 4 Finger Lakes Not Assessed Not Assessed 5 Long Island Invasive Species Management Area Not Present Moderate 6 Lower Hudson Not Assessed Not Assessed 7 Saint Lawrence/Eastern Lake Ontario Not Assessed Not Assessed 8 Western New York Not Assessed Not Assessed Invasiveness Ranking Summary Total (Total Answered*) Total (see details under appropriate sub-section) Possible 1 Ecological impact 40 ( 40 ) 37 2 Biological characteristic and dispersal ability 25 ( 25 ) 20 3 Ecological amplitude and distribution 25 ( 25 ) 4 4 Difficulty of control 10 ( 10 ) 8 Outcome score 100 ( 100 )b 73.00 a † Relative maximum score 73.00 § New York Invasiveness Rank High (Relative Maximum Score 70.00-80.00) * For questions answered “unknown” do not include point value in “Total Answered Points Possible.” If “Total Answered Points Possible” is less than 70.00 points, then the overall invasive rank should be listed as “Unknown.” †Calculated as 100(a/b) to two decimal places. -
(Amaranthaceae) in Italy. V. Atriplex Tornabenei
Phytotaxa 145 (1): 54–60 (2013) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2013 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.145.1.6 Studies on the genus Atriplex (Amaranthaceae) in Italy. V. Atriplex tornabenei DUILIO IAMONICO1 1 Laboratory of Phytogeography and Applied Geobotany, Department PDTA, Section Environment and Landscape, University of Rome Sapienza, 00196 Roma, Italy. Email: [email protected] Abstract The typification of the name Atriplex tornabenei (a nomen novum pro A. arenaria) is discussed. An illustration by Cupani is designated as the lectotype, while a specimen from FI is designated as the epitype. Chorological and morphological notes in comparison with the related species A. rosea and A. tatarica are also provided. A nomenclatural change (Atriplex tornabenei subsp. pedunculata stat. nov.) is proposed. Key words: Atriplex tornabenei var. pedunculata, epitype, infraspecific variability, lectotype, Mediterranean, nomenclatural change, nomen novum Introduction Atriplex Linnaeus (1753: 1054) is a genus of about 260 species distributed in arid and semiarid regions of Eurasia, America and Australia (Sukhorukov & Danin 2009). Several names (at species, subspecies, variety and form ranks) were described related to the high phenotipic variability of this critical genus (Al-Turki et al. 2000). As conseguence, misapplication of names and nomenclatural disorders exist and need clarification. In this paper, the identity of the A. tornabenei Tineo ex Gussone (1843: 589) is discussed as part of the treatment of the genus Atriplex for the new edition of the Italian Flora (editor, Prof. S. Pignatti) and within the initiative “Italian Loci Classici Census” (Domina et al. -
Understanding the Weedy Chenopodium Complex in the North Central States
UNDERSTANDING THE WEEDY CHENOPODIUM COMPLEX IN THE NORTH CENTRAL STATES BY SUKHVINDER SINGH DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Crop Sciences in the Graduate College of the University of Illinois at Urbana-Champaign, 2010 Urbana, Illinois Doctoral Committee: Professor Patrick J. Tranel, Chair Associate Professor Aaron G. Hager Associate Professor Geoffrey A. Levin Assistant Professor Matthew E. Hudson ABSTRACT The genus Chenopodium consists of several important weed species, including Chenopodium album, C. berlandieri, C. strictum, and C. ficifolium. All of these species share similar vegetative morphology and high phenotypic plasticity, which makes it difficult to correctly identify these species. All of these weedy Chenopodium species have developed resistance to one or more classes of herbicides. An experiment was conducted to determine if there is variability in response of Chenopodium species present in the North Central states to glyphosate. Our results indicate variable responses within and among the Chenopodium species. Species such as C. berlandieri and C. ficifolium had higher levels of tolerance to glyphosate than did various accessions of C. album. In another experiment, 33 populations of Chenopodium sampled across six North Central states were screened with glyphosate. The results showed variable responses to glyphosate within and among the Chenopodium populations. In general, the Chenopodium populations from Iowa were more tolerant, but some biotypes from North Dakota, Indiana and Kansas also had significantly high tolerance to glyphosate. Given there are species other than C. album that have high tolerance to glyphosate, and there are Chenopodium populations across the North Central states that showed tolerance to glyphosate, one intriguing question was to whether the Chenopodium populations were either biotypes of C. -
Amaranthaceae Amaranth Family
Amaranthaceae Amaranth Family Mostly ruderal annuals, there are 900 species in 65 genera. A single genus reaches Nova Scotia. Their flowers are inconspicuous, green and apetalous, subtended by papery bracts. Flowers are unisexual Page | 108 although the plants are monoecious. The terminal inflorescence is brushlike or axillary. A single lens- shaped achene is produced. Some are flowering ornamentals, such as Celosia and Love-lies-bleeding (Amaranthus caudatus) and others are used for grain. Amaranthus L. Three of 50 species have been introduced into Nova Scotia. Key to species A. A. Plants slender, branching diffusely; flowers in small axillary clusters; Amaranthus albus seeds small, <0.8mm wide. aa. Plants robust, erect; flowers in large terminal inflorescences; seeds >1mm B wide. B. Leaves green beneath; sepals pointed. A. hybridus bb. Leaves whitish beneath; sepals truncate. A. retroflexus Amaranthus albus L. Tumbleweed; amarante blanche An erect herb, its stems are freely branching. Leaves are elliptic or oblanceolate, borne on petioles. Flowers are arranged in dense axillary clusters. July to October, on disturbed soils. Uncommon and appearing as a garden weed or about railways. Collected from Truro, Wentworth, Windsor and Kentville. Ranges from western Canada to Mexico. Introduced throughout most of the continent. 3-2 Amaranthaceae Amaranthus hybridus L. Green Amaranth; amarante verte Tall and robust, its stem reaches to 2m in height, often branching freely. Stems are scaly or lightly pubescent Page | 109 especially in the inflorescence. Flowers are reddish, not showy. Leaves are elliptic and petiolate. August to October. A weed of disturbed soils and cultivated fields. It is limited to a few well-established populations: Morristown and other communities in Kings Co. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Beta Vulgaris (Common Beet) Class:Magnoliopsida Order
Beta vulgaris (Common Beet) Class:Magnoliopsida Order: Caryophyllales Family: Amaranthaceae Genus: Beta Species: Beta vulgaris Beet seeds Common Varieties: Bull’s Blood, Golden, Chioggia, Detroit Dark Red How to Save Seed Beets are a biennial crop, meaning they require two years to complete their full growing cycle. However, most growers never see this second stage of life because beets are harvested for food during the first year. The second year heralds seed production. To save the seeds from beta vulgaris, the beets themselves must be overwintered. This process, unique to perennial and biennial crops, requires that the taproot of the beta vulgaris (the edible part of the beet) be stored in a protected place during the winter months. A Seed Saving Guide asserts that the optimal temperature range for winter storage is between 35-38F at 90-95% humidity. The roots may be stored in sawdust or wood shavings to minimize rot. This allows the plant to enter a period of dormancy—during this time, the plant’s energy will be diverted to the next year’s seed production. In Spring, plant the overwintered beets outside in a well-watered trench. Because beets are wind-pollinated, they should be planted in a block formation rather than a straight row to ensure proper pollination. The Seed Saver’s Exchange Seed Saving Guide specifies that the isolation distance (the distance between different varieties of beets) must be over 800 feet. Adhering to this distance is critical—without it, there is potential for varieties to cross-pollinate, meaning the genetic integrity of the beet variety will be compromised. -
Table 4: Pollen-Types in Amaranthaceae by Mittre (1963). Amaranthus-Type
Table 4: Pollen-types in Amaranthaceae by Mittre (1963). Amaranthus-type Amaranthus- type sensu stricto Cyathula-type Celosia-type Pollen Faintly to moderately granulate Prominently granulate Baculariate morphological characters: Sexine pattern Total number of 5 2 2 genera studied Genera Amaranthus spinosus L., Cyathula prostrate (L.) Blume, Celosia argentea L., C. cristata L., A. viridis L., A. tricolor L., C. capitata Moq., Allmania albida (Willd.) R.Br. ex Hook.f., A. hybridus L., Deeringia celosioides R.Br. A. nodiflora (L.) R.Br. ex Wight. A. polygamous L., A. tenuifolius Willd., A. spinosus L., Achyranthes aspera L., A. bidentata Blume, Aerva lanata (L.) Juss., A. sanguinolenta (L.) Blume, A. tomentosa Forssk., A. javanica (Burm.f.) Juss. ex Schult., A. monsoniae (L. f.) Mart., Digera arvensis Forssk., Pupalia lappacea (L.) Juss., P. atropurpurea (Lam.) Moq. 22 Table 4: Continued. Gomphrena-type Gomphrena-type sensu stricto Alternanthera-type Not included in any group Pollen reticulate several meshes, without reticulate with few meshes, without reticulate with several meshes and spinulate morphological spinules spinules characters: Sexine pattern Total number of 1 1 1 genera studied Genera Gomphrena globosa L., Alternanthera sessilis (L.) R.Br. ex DC., Psilotrichum ferrugineum (Roxb.) Moq. G. celosioides Mart. A. repens J.F.Gmel. 2 3 Table 5: Pollen-types in Centrospermae by Nowicke (1975). Type I Type II Type III Pollen morphological 3- Colpate Pantoporate Pantocolpate characters: apertures Family studied Aizoaceae, Cactaceae, Caryophyllaceae, Amaranthaceae, Cactaceae, Basellaceae, Cactaceae, Molluginaceae, Nyctaginaceae, Caryophyllaceae, Chenopodiaceae, Molluginaceae, Nyctaginaceae, Phytolaccaceae, Portulacaceae Dysphaniaceae, Nyctaginaceae, Phytolaccaceae, Portulacaceae Phytolaccaceae, Portulacaceae Genera studied in 11 Amaranthaceae Species studied in Amaranthus spinosus L., Amaranthaceae Aerva leucura Moq., Allmania nodiflora (L.) R.Br. -
Beta Vulgaris: a Systematic Review
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by shahrekord university of medical scinces Available online a t www.scholarsresearchlibrary.com Scholars Research Library Der Pharmacia Lettre, 2016, 8 (19):404-409 (http://scholarsresearchlibrary.com/archive.html) ISSN 0975-5071 USA CODEN: DPLEB4 Chemistry and pharmacological effect of beta vulgaris: A systematic review Sepide Miraj M.D., Gynecologist, Fellowship of Infertility, Assistant Professor, Faculty of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran _____________________________________________________________________________________________ ABSTRACT Beta vulgaris is a plant native to Mediterranean, the Atlantic coast of Europe, the Near East, and India belong to Amaranthaceae, Genus Beta, and Subfamily Betoideae. The aim of this study is to overview Chemistry and pharmacological effect of beta vulgaris . This review article was carried out by searching studies in PubMed, Medline, Web of Science, and IranMedex databases up to 201 6.Among 89 found articles, 54 articles were included. The search terms were “Beta vulgaris”, “therapeutic”, and “pharmacological”, "Chemistry ". Various studies have shown that Beta vulgaris possess anti-inflammatory effect, antioxidant Properties, anti-stress effect, anti-Anxiety and anti-depressive effect, anti-cancer, antihypertensive effect, hydrophobic properties, anti-sterility effects. The result of this study have found various constituents of Beta vulgaris exhibit a variety of therapeutic -
An Uninhabited, Undeveloped Barrier Island. (Under the Direction of Thomas R
ABSTRACT ROSENFELD, KRISTEN MARIE. Ecology of Bird Island, North Carolina: an uninhabited, undeveloped barrier island. (Under the direction of Thomas R. Wentworth.) Barrier islands include some of the most endangered and fragmented ecosystems on the Atlantic coast, providing critical habitat for many species, including some that are threatened and endangered. As the vast majority of these islands have been developed for human usage study and protection of the few remaining undeveloped and undisturbed islands is critical. This study was undertaken in order to characterize the vascular plant communities on Bird Island, an uninhabited, undeveloped barrier island on the border of North and South Carolina, with the objectives of a thorough survey of flora, vegetation, and environment, classification of plant communities, and multivariate analysis of vegetation and environmental data. A floristic inventory of the island and its associated marshes was conducted during the growing season (May- November) of 2002 and 2003. One hundred four 100m2 plots were inventoried for vegetation and environment using protocols developed by the Carolina Vegetation Survey. Plant communities were identified according to the National Vegetation Classification, the Classification of the Natural Communities of North Carolina, and the Carolina Vegetation Survey. Interpretation of vegetation patterns was based on multivariate analysis of vegetation and environmental data. Ninety-one vascular plant species in 35 families, including 4 exotic species, were distributed across 12 communities. Communities on Bird Island appear to be distinctive when compared to those described for other barrier islands in the region. Additionally, the vegetation survey on Bird Island revealed suitable habitat for the federally listed Seabeach amaranth (Amaranthus pumilus); an important dune-building annual of the North American Atlantic coast. -
Guide to the Genera of Lianas and Climbing Plants in the Neotropics
GUIDE TO THE GENERA OF LIANAS AND CLIMBING PLANTS IN THE NEOTROPICS AMARANTHACEAE By Pedro Acevedo-Rodríguez (1 August 2018) A predominantly tropical family of herbs, sub-shrubs, shrubs and rarely trees, some herbs or shrubs are scandent and a few species are twining lianas. Generally found in moist to humid areas below 1400 m elevation with a few species reaching 2700 m. The family is represented in the Neotropics by ca. 490 species of which 25 are consistently reported as climbers that reach two or more m in length. Iresine, contain several species that are scandent herbs; Chamissoa and Pleuropetalum a species each that are scandent shrubs; Gomphrena, Hebanthe, and Pedersenia have species that are twining lianas and sometimes scandent shrubs with elongated stems. Gomphrena vaga (photo by P. Acevedo) Diagnostics: In the absence of fertile material, climbing Amaranthaceae are sometimes confused with Asteraceae or Acanthaceae. However, woody Amaranthaceae, i.e., scandent shrubs and twining lianas, are easily identified by the cylindrical stems with successive rings of xylem and phloem and by the presence of swollen nodes. The leaves are opposite or alternate depending on the genus, with entire margins, gland-less blades and petioles, and lack stipules. Fruits are circumscissile utricles. General Characters 1. STEMS. Stems are cylindrical, herbaceous in Iresine or woody in Chamissoa, Gomphrena, Hebanthe, Pedersenia, and Pleuropetalum. Herbaceous stems usually are 5 mm or less in diam., and up to 3 m in length; stems of woody species are 1 to 3 cm in diam. and up to 15 m in length. Stems usually present a large medulla, and successive rings of xylem and phloem are known to occur in most genera, however, these are more conspicuous in woody taxa (fig.1a, b).