Notes on the Occurrence of Erigeron Sumatrensis (Asteraceae) in Georgia
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The Ecology of Fleabane (Conyza Spp.)
The ecology of fleabane (Conyza spp.) Todd Douglas Green B.LandMgmt(Ecological Agriculture) University of Sydney B.Sc (Hons) University of Newcastle A thesis submitted for the degree of Doctor of Philosophy of the University of New England School of Environmental and Rural Science Faculty of Arts and Sciences University of New England October 2010 DECLARATION I certify that the substance of this thesis has not already been submitted for any degree and is not currently being submitted for any other degree or qualification. I certify that any help received in preparing this thesis, and all sources used, have been acknowledged in this thesis. Todd Douglas Green i ACKNOWLEDGEMENTS I would like to acknowledge the Cotton Research Development Corporation (CRDC) and the Cotton Catchment Communities Co-operative Research Centre (Cotton CRC) for funding this research (Project #1.01.54) and thank these entities for offering me an opportunity to undertake a PhD. My supervisory team of Professor Brian Sindel, Dr Jeff Werth and Mr Graham Charles all played a role in getting my research completed and thesis submitted. I thank them all for supporting my journey over the past three years. I am grateful for the detailed reviews and editing by Professor Sindel, his encouragement, knowledge and understanding. I would like to thank Dr Jeff Werth for his promptness in feedback, knowledge and his encouragement. To Mr Graham Charles, I am fortunate to have access to his practical knowledge and thank him for his thorough reviews and encouragement. I would also like to thank general staff members of the University of New England who provided assistance to me personally and for practical elements of my research, namely, Dan Alter, Greg (‘Tractor’) Chamberlain, Mick Faint, George Henderson, Dave Edmonds and Elizabeth Davies. -
V. Vladimirov, V. Matevski, S. Bancheva, M. Delcheva, M
Fl. Medit. 26: 203-207 doi: 10.7320/FlMedit26.203 Version of Record published online on 30 December 2016 V. Vladimirov, V. Matevski, S. Bancheva, M. Delcheva, M. Kostadinovski & R. Ćušterevska First report of Erigeron sumatrensis (Asteraceae) for the flora of the Republic of Macedonia Abstract Vladimirov, V., Matevski, V., Bancheva, S., Delcheva, M., Kostadinovski, M. & Ćušterevska, R.: First report of Erigeron sumatrensis (Asteraceae) for the flora of the Republic of Macedonia. — Fl. Medit. 26: 203-207. 2016. — ISSN: 1120-4052 printed, 2240-4538 online. Erigeron sumatrensis (Asteraceae) is reported for the first time for the flora of the Republic of Macedonia. The taxon was recorded in several localities across the country. It seems, the species was introduced several decades ago, however, it remained unrecognized, mainly due to mis-identification with E. bonariensis. Brief morphological description, based on the material collected from Macedonia, and the habitat preferences of the species are provided. Erigeron sumatrensis has viable and persistent populations and should be regarded as naturalized in the Macedonian flora. The invasive behavior of the species is discussed briefly. Key words: alien plants, Conyza, Conyza sumatrensis, Macedonian flora, xenophytes. Introduction Although the flora of the Republic of Macedonia is relatively well studied, ongoing research into the plant diversity of the county for the preparation of the critical national Flora continues to provide floristic novelties. Recently, four new taxa – Andrachne tele- phioides L., Chorispora tenella (Pallas) DC., Nepeta parviflora M. Bieb. and Marrubium pestalozzae Boiss. – were reported (Matevski 2016). During field studies within a bilateral Bulgarian-Macedonian project devoted to the taxonomic diversity in the families Lamiaceae and Asteraceae, a new alien species for the Macedonian flora was recorded next to a petrol station near the highway in Veles Municipality – Erigeron sumatrensis Retz. -
ISB: Atlas of Florida Vascular Plants
Longleaf Pine Preserve Plant List Acanthaceae Asteraceae Wild Petunia Ruellia caroliniensis White Aster Aster sp. Saltbush Baccharis halimifolia Adoxaceae Begger-ticks Bidens mitis Walter's Viburnum Viburnum obovatum Deer Tongue Carphephorus paniculatus Pineland Daisy Chaptalia tomentosa Alismataceae Goldenaster Chrysopsis gossypina Duck Potato Sagittaria latifolia Cow Thistle Cirsium horridulum Tickseed Coreopsis leavenworthii Altingiaceae Elephant's foot Elephantopus elatus Sweetgum Liquidambar styraciflua Oakleaf Fleabane Erigeron foliosus var. foliosus Fleabane Erigeron sp. Amaryllidaceae Prairie Fleabane Erigeron strigosus Simpson's rain lily Zephyranthes simpsonii Fleabane Erigeron vernus Dog Fennel Eupatorium capillifolium Anacardiaceae Dog Fennel Eupatorium compositifolium Winged Sumac Rhus copallinum Dog Fennel Eupatorium spp. Poison Ivy Toxicodendron radicans Slender Flattop Goldenrod Euthamia caroliniana Flat-topped goldenrod Euthamia minor Annonaceae Cudweed Gamochaeta antillana Flag Pawpaw Asimina obovata Sneezeweed Helenium pinnatifidum Dwarf Pawpaw Asimina pygmea Blazing Star Liatris sp. Pawpaw Asimina reticulata Roserush Lygodesmia aphylla Rugel's pawpaw Deeringothamnus rugelii Hempweed Mikania cordifolia White Topped Aster Oclemena reticulata Apiaceae Goldenaster Pityopsis graminifolia Button Rattlesnake Master Eryngium yuccifolium Rosy Camphorweed Pluchea rosea Dollarweed Hydrocotyle sp. Pluchea Pluchea spp. Mock Bishopweed Ptilimnium capillaceum Rabbit Tobacco Pseudognaphalium obtusifolium Blackroot Pterocaulon virgatum -
Erigeron Speciosus (Lindl.) DC
ASPEN FLEABANE Erigeron speciosus (Lindl.) DC. Asteraceae – Aster family Corey L. Gucker & Nancy L. Shaw | 2018 ORGANIZATION NOMENCLATURE Erigeron speciosus (Lind.) DC., hereafter Names, subtaxa, chromosome number(s), hybridization. referred to as aspen fleabane, belongs to the Astereae tribe of the Asteraceae or aster family (Nesom 2006). Range, habitat, plant associations, elevation, soils. NRCS Plant Code. ERSP4 (USDA NRCS 2018). Synonyms. Erigeron conspicuus Rydberg; E. macranthus Nuttall; E. speciosus var. conspicuus (Rydberg) Breitung; E. speciosus Life form, morphology, distinguishing characteristics, reproduction. var. macranthus (Nuttall) Cronquist; E. subtrinervis Rydberg ex Porter & Britton subsp. conspicuus (Rydberg) Cronquist; Growth rate, successional status, disturbance ecology, importance to E. subtrinervis var. conspicuus (Rydberg) animals/people. Cronquist, Stenactis speciosa Lindley (Nesom 2006). Current or potential uses in restoration. Common Names. Aspen fleabane, Oregon fleabane, Oregon wild-daisy, showy daisy, showy fleabane (USDA FS 1937; Nesom 2006; AOSA 2016; USDA NRCS 2018). Seed sourcing, wildland seed collection, seed cleaning, storage, testing and marketing standards. Subtaxa. No varieties or subspecies are currently recognized by the Flora of North America (Nesom 2006). Recommendations/guidelines for producing seed. Chromosome Number. Chromosome numbers are 2n = 18, 36 (Jones and Young 1983; Welsh et al. 1987). Recommendations/guidelines for producing planting stock. Hybridization. Distributions of aspen fleabane and threenerve fleabane (E. subtrinervis) have considerable overlap, and although they are Recommendations/guidelines, wildland restoration successes/ considered at least partially reproductively failures. isolated, intermediate forms are common (Nesom 2006). Primary funding sources, chapter reviewers. DISTRIBUTION Bibliography. Aspen fleabane is widely distributed throughout western North America. In Canada, it occurs in British Columbia and Alberta. -
Chemical Constituents from Erigeron Bonariensis L. and Their Chemotaxonomic Importance
SHORT REPORT Rec. Nat. Prod . 6:4 (2012) 376-380 Chemical Constituents from Erigeron bonariensis L. and their Chemotaxonomic Importance Aqib Zahoor 1,4 , Hidayat Hussain *1,2 , Afsar Khan 3, Ishtiaq Ahmed 1, Viqar Uddin Ahmad 4 and Karsten Krohn 1 1Department of Chemistry, Universität Paderborn, Warburger Straße 100, 33098 Paderborn, Germany 2Department of Biological Sciences and Chemistry, University of Nizwa, P.O Box 33, Postal Code 616, Birkat Al Mauz, Nizwa, Sultanate of Oman 3Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad-22060, Pakistan. 4H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270, Pakistan. (Received September 11, 2011; Revised May 9, 2012 Accepted June 15, 2012) Abstract: The study of the chemical constituents of the whole plant of Erigeron bonariensis (L.) has resulted in the isolation and characterization of a new and nine known compounds. The known compounds were identified as stigmasterol (1), freideline ( 2), 1,3-dihydroxy-3R,5 R-dicaffeoyloxy cyclohexane carboxylic acid methyl ester ( 3), 1R,3 R-dihydroxy- 4S,5 R-dicaffeoyloxycyclohexane carboxylic acid methyl ester ( 4), quercitrin ( 5), caffeic acid ( 6), 3-(3,4- dihydroxyphenyl)acrylic acid 1-(3,4-dihydroxyphenyl)-2-methoxycarbonylethyl ester (8), benzyl O-β-D-glucopyranoside (9), and 2-phenylethyl-β-D-glucopyranoside ( 10 ). The aromatic glycoside, erigoside G ( 7) is reported as new natural compound. The above compounds were individually identified by spectroscopic analyses and comparisons with reported data. The chemotaxonomic studies of isolated compounds have been discussed. Keywords: Erigeron bonariensis ; natural products; chemotaxonomic studies. 1.Plant Source Erigeron bonariensis (L.) is locally called “gulava” or “mrich booti” and is traditionally used in urine problems. -
Essential Oil Compositions of Three Invasive Conyza Species Collected in Vietnam and Their Larvicidal Activities Against Aedes A
molecules Article Essential Oil Compositions of Three Invasive Conyza Species Collected in Vietnam and Their Larvicidal Activities against Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus Tran Minh Hoi 1, Le Thi Huong 2 , Hoang Van Chinh 3, Dang Viet Hau 4, Prabodh Satyal 5, Thieu Anh Tai 6, Do Ngoc Dai 7,8 , Nguyen Huy Hung 6,9,* , Vu Thi Hien 10 and William N Setzer 5,11,* 1 Department of Plant Resources, Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam; [email protected] 2 School of Natural Science Education, Vinh University, 182 Le Duan, Vinh City 43000, Vietnam; [email protected] 3 Faculty of Natural Sciences, Hong Duc University, 365 Quang Trung, Thanh Hoa 440000, Vietnam; [email protected] 4 Center for Research and Technology Transfer, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam; [email protected] 5 Aromatic Plant Research Center, 230 N 1200 E, Suite 102, Lehi, UT 84043, USA; [email protected] 6 Department of Pharmacy, Duy Tan University, 03 Quang Trung, Da Nang 550000, Vietnam; [email protected] 7 Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18-Hoang Quoc Viet, Cau Giay, Hanoi, 100000 Vietnam; [email protected] 8 Faculty of Agriculture, Forestry and Fishery, Nghe An College of Economics, 51-Ly Tu Trong, Vinh City 460000, Vietnam 9 Center for Advanced Chemistry, Institute of Research and Development, Duy Tan University, 03 Quang Trung, Da Nang 550000, Vietnam -
Flora Mediterranea 26
FLORA MEDITERRANEA 26 Published under the auspices of OPTIMA by the Herbarium Mediterraneum Panormitanum Palermo – 2016 FLORA MEDITERRANEA Edited on behalf of the International Foundation pro Herbario Mediterraneo by Francesco M. Raimondo, Werner Greuter & Gianniantonio Domina Editorial board G. Domina (Palermo), F. Garbari (Pisa), W. Greuter (Berlin), S. L. Jury (Reading), G. Kamari (Patras), P. Mazzola (Palermo), S. Pignatti (Roma), F. M. Raimondo (Palermo), C. Salmeri (Palermo), B. Valdés (Sevilla), G. Venturella (Palermo). Advisory Committee P. V. Arrigoni (Firenze) P. Küpfer (Neuchatel) H. M. Burdet (Genève) J. Mathez (Montpellier) A. Carapezza (Palermo) G. Moggi (Firenze) C. D. K. Cook (Zurich) E. Nardi (Firenze) R. Courtecuisse (Lille) P. L. Nimis (Trieste) V. Demoulin (Liège) D. Phitos (Patras) F. Ehrendorfer (Wien) L. Poldini (Trieste) M. Erben (Munchen) R. M. Ros Espín (Murcia) G. Giaccone (Catania) A. Strid (Copenhagen) V. H. Heywood (Reading) B. Zimmer (Berlin) Editorial Office Editorial assistance: A. M. Mannino Editorial secretariat: V. Spadaro & P. Campisi Layout & Tecnical editing: E. Di Gristina & F. La Sorte Design: V. Magro & L. C. Raimondo Redazione di "Flora Mediterranea" Herbarium Mediterraneum Panormitanum, Università di Palermo Via Lincoln, 2 I-90133 Palermo, Italy [email protected] Printed by Luxograph s.r.l., Piazza Bartolomeo da Messina, 2/E - Palermo Registration at Tribunale di Palermo, no. 27 of 12 July 1991 ISSN: 1120-4052 printed, 2240-4538 online DOI: 10.7320/FlMedit26.001 Copyright © by International Foundation pro Herbario Mediterraneo, Palermo Contents V. Hugonnot & L. Chavoutier: A modern record of one of the rarest European mosses, Ptychomitrium incurvum (Ptychomitriaceae), in Eastern Pyrenees, France . 5 P. Chène, M. -
Morphology, Anatomy, Palynology and Achene Micromorphology of Bellis L. (Asteraceae) Species from Turkey
Acta Bot. Croat. 79 (1), 59–67, 2020 CODEN: ABCRA 25 DOI: 10.37427/botcro-2020-006 ISSN 0365-0588 eISSN 1847-8476 Morphology, anatomy, palynology and achene micromorphology of Bellis L. (Asteraceae) species from Turkey Faruk Karahan* Department of Biology, Faculty of Science and Arts, Hatay Mustafa Kemal University, 31040 Hatay, Turkey Abstract – In the present study, the morphological characters, root, stem and leaf anatomy, pollen and achene micromorphology of Bellis L. species (Bellis annua L., B. perennis L. and B. sylvestris Cirillo) distributed in Turkey have been investigated on light and scanning electron microscope. Palynological analysis showed that pollen characters were found as small to medium size, isopolar, radially symmetrical, oblate-spheroidal and prolate- spheroidal, tricolporate and echinate-perforate ornamentation in the three species. Achene characters were found dark brown to yellow in colour, often cylindrical, compressed, with thickened margin, obovate orobovoid shaped, pappus absent and the coat ornamentations are rectangular with short hairs on the surface. As a result of this study, leaf morphology and some pollen characteristics such as pollen size, shape, perforation and distance be- tween spines were demonstrated to be different among the Bellis species. Keywords: Bellis, common daisy, Compositae, taxonomy, SEM Introduction The genus Bellis L. (Asteraceae) has been included in the Fiz et al. (2002) studied the phylogenetic relationships subtribe Bellidinae Willk. (tribe Astereae Cass.) along with between Bellis and the closely related genera (Bellidastrum 117 other genera representing more than 3000 annual or Scop, Bellium L. and Rhynchospermum Lindl.) and evolu- perennial taxa (Bremer 1994). It is native to western, cen- tion of their morphological characters. -
Genotypic Diversity and Clonal Structure of Erigeron Annuus
26. Deutsche Arbeitsbesprechung über Fragen der Unkrautbiologie und -bekämpfung, 11.-13. März 2014 in Braunschweig Genotypic diversity and clonal structure of Erigeron annuus (Asteraceae) in Lithuania Genetische Vielfalt und Klonstruktur von Erigeron annuus (Asteraceae) in Litauen Virginija Tunaitienė1*, Jolanta Patamsytė1, Tatjana Čėsnienė1, Violeta Kleizaitė1, Donatas Naugžemys2, Vytautas Rančelis1 and Donatas Žvingila1 1Department of Botany and Genetics, Vilnius University, M. K. Čiurlionio 21, Vilnius, Lithuania 2Botanical Garden of Vilnius University, Kairėnų 43, Vilnius, Lithuania *Corresponding author, [email protected] DOI 10.5073/jka.2014.443.023 Abstract This study was conducted to assess the clonal structure and genetic diversity of alien herbaceous plant species Erigeron annuus. The global warming and changes in agriculture practice in the past few decades were favourable for the expansion of this species in Lithuania. We used RAPD and ISSR assays to assess genetic variation within and among 29 populations of E. annuus. A total of 278 molecular markers were revealed. Our study detected reduced level of genetic diversity of invasive populations of E. annuus. Significant differences in DNA polymorphism among populations of E. annuus were also found. Some populations of this species are composed of genetically identical plants, while others were polymorphic. Clonal diversity of study populations ranged from 0.083 to 0.4 for both DNA marker systems. The Simpsons diversity index values ranged from 0.0 to 0.636. The average number of genotypes per population established using both assays was about 1.7. Out of 328 E. annuus individuals only 16 showed unique RAPD and 14 unique ISSR banding patterns. The remaining plants were clones of different size. -
Open-Pollinated Transfer of Glyphosate Resistance in Horseweed (Conyza Canadensis) in Greenhouse Isolation Ryan S
Open-Pollinated Transfer of Glyphosate Resistance in Horseweed (Conyza canadensis) in Greenhouse Isolation Ryan S. Henry, Vince M. Davis, William G. Johnson Department of Botanyygy,y and Plant Pathology, Purdue University Introduction Results Horseweed (Conyza canadensis) has become a problematic weed in crop production fields across the United States. The fraction of the population that is resistant to the herbicide glyphosate continues to increase each year. In Indiana, farmers have ranked horseweed as a top-five problematic weed, and a field survey found 38% of the population of horseweed to be glyphosate-resistant (GR) in southeastern Indiana. A single- locus, nuclear encoded gene confers glyphosate resistance (Zelaya et al. 2004). Horseweed primarily self pollinates, but nuclear encoded paraquat resistance out-crosses at Figure 1. GR and GS F horseweed progeny 35 DAT -1 1 Figure 2. GR and GS F2 horseweed progeny 28 DAT with 0.84 kg ae ha approximately 4% under field conditions (Smisek 1995). The with 0.84 kg ae ha-1 glyphosate. glyphosate, and example of green value analysis with ImageJ software. transfer of glyphosate resistance via pollen as a mechanism of gene flow, in addition to long distance seed movement, is -1 Table 1 Response of first (F1) and second (F2) generation horseweed progeny to 0.84 kg ae ha glyphosate for open troubling because it could aid in the evolution of multiple and manually cross pollinated horseweed. Green pixel value was determined by digital image analysis program. resistance. Horseweed Glyphosate- Glyphosate- Biotypes resistant susceptible Objective Cross Green Green The objective of this experiment was to quantify the potential for pollination pixel Std. -
Erigeron Howellii Asteraceae Rays Relatively Broad, Howell's Daisy, Howell's Fleabane White Or Pinkish
Erigeron howellii Asteraceae rays relatively broad, Howell's daisy, Howell's fleabane white or pinkish Gerald D. Carr Gerald D. Carr involucral bracts long and acuminate disk floret corollas flared achenes short and hairy, mostly 5 nerved Gerald D. Carr Gerald D. Carr plants 20-50 cm tall Illustration by Jeanne R. Janish. VASCULAR PLANTS OF THE PACIFIC NORTHWEST (1955) Hitchcock, Cronquist, & Ownbey, courtesy of University of Washington Press. Herbaceous perennial from a short rhizome, 20-50cm tall. Stems slender, erect, glabrous, scantily short-villous under the heads. Leaves are shiny dark green, thin and glabrous, alternate, entire, ovate or obovate, lower leaves with 2-12 cm petiole connecting directly to the blade, upper leaves strongly clasp- ing at the base. Inflorescence solitary head, disk 12-20 mm wide, involucral bracts long, acuminate, loose, equal, glandular and somewhat herbaceous, rays relatively broad, 30-50, white or pinkish; disk corollas 4-5 mm long and distinctly flared, pappus simple, coarse and fragile about 20-30 bristles. Fruits achenes, short, hairy, mostly asymmetrically 5 nerved. Lookalikes differs from featured plant by Erigeron peregrinus its disk corollas not as flared, ray flowers usually pink best survey times to purple. J | F | M | A | M | J | J | A | S | O | N | D Erigeron howellii (A. Gray) A. Gray Howell's daisy, Howell's fleabane PLANTS symbol: ERHO3 August 2019 status Oregon:C; ORBIC: List 1 Distribution: Columbia River Gorge, Multnomah, Hood River and Clackamas Counties, OR and Skamania County, WA. Habitat: Often found in moist, rocky sites, on protected slopes within mixed coniferous forests. -
Effects of Residence Time, Auto-Fertility and Pollinator
plants Article Effects of Residence Time, Auto-Fertility and Pollinator Dependence on Reproductive Output and Spread of Alien and Native Asteraceae Anna Corli 1,2 and Christine S. Sheppard 1,* 1 Institute of Landscape and Plant Ecology, University of Hohenheim, August-von-Hartmann Str. 3, 70599 Stuttgart, Germany; [email protected] 2 Department of Earth and Environmental Sciences, University of Pavia, Pavia, Via S. Epifanio 14, 27100 Pavia, Italy * Correspondence: [email protected] Received: 18 March 2019; Accepted: 18 April 2019; Published: 23 April 2019 Abstract: Alien plants benefit from auto-fertility to spread over areas where the lack of co-evolved mutualists would otherwise limit invasion success. However, the widespread generalists among mutualists and their large geographical ranges allow alien plants to be integrated into networks. The role of residence time also has to be accounted for, as it takes time for a species to spread and adapt to a new area. We investigated how residence time, auto-fertility and pollinator dependence affect reproductive output and invasion success of Asteraceae in Germany. We conducted a multi-species common-garden experiment along an alien–native continuum including 42 species of natives, archaeophytes and neophytes (casual and established), subjecting plant individuals either to free access or exclusion of pollinators. Pollinator dependence does not play a crucial role in invasion success, with most Asteraceae being able to self-fertilize. Surprisingly, both established neophytes and natives showed higher abilities to self-fertilize, while archaeophytes and casual neophytes were more attractive to pollinators. In contrast to casual neophytes, the established neophytes’ strategy was associated with a large reproductive output.