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Diversity of Rhizobia Associated with Amorpha Fruticosa Isolated from Chinese Soils and Description of Mesorhizobium Amorphae Sp
International Journal of Systematic Bacteriology (1999), 49, 5 1-65 Printed in Great Britain Diversity of rhizobia associated with Amorpha fruticosa isolated from Chinese soils and description of Mesorhizobium amorphae sp. nov. E. T. Wang,lt3 P. van Berkum,2 X. H. SU~,~D. Beyene,2 W. X. Chen3 and E. Martinez-Romerol Author for correspondence : E. T. Wang. Tel : + 52 73 131697. Fax: + 52 73 175581. e-mail: [email protected] 1 Centro de lnvestigacidn Fifty-five Chinese isolates from nodules of Amorpha fruticosa were sobre Fijaci6n de characterized and compared with the type strains of the species and genera of Nitrdgeno, UNAM, Apdo Postal 565-A, Cuernavaca, bacteria which form nitrogen-f ixing symbioses with leguminous host plants. A Morelos, Mexico polyphasic approach, which included RFLP of PCR-amplified 165 rRNA genes, * Alfalfa and Soybean multilocus enzyme electrophoresis (MLEE), DNA-DNA hybridization, 165 rRNA Research Laboratory, gene sequencing, electrophoretic plasmid profiles, cross-nodulation and a Ag ricuI tu ra I Research phenotypic study, was used in the comparative analysis. The isolates Service, US Department of Agriculture, BeltsviI le, M D originated from several different sites in China and they varied in their 20705, USA phenotypic and genetic characteristics. The majority of the isolates had 3 Department of moderate to slow growth rates, produced acid on YMA and harboured a 930 kb Microbiology, College of symbiotic plasmid (pSym). Five different RFLP patterns were identified among Biology, China Agricultural the 16s rRNA genes of all the isolates. Isolates grouped by PCR-RFLP of the 165 University, Beijing 100094, People’s Republic of China rRNA genes were also separated into groups by variation in MLEE profiles and by DNA-DNA hybridization. -
Japanese Knotweed Fallopia Japonica (Houtt.) R. Decr. Or Polygonum Cuspidatum Sieb
Japanese knotweed Fallopia japonica (Houtt.) R. Decr. or Polygonum cuspidatum Sieb. & Zucc. Giant knotweed Fallopia sachalinensis (F. Schmidt ex Maxim.) R. Decr. or Polygonum sachalinense F. Schmidt ex Maxim. Bohemian knotweed Fallopia × bohemica (Chrtek & Chrtková) J. P. Bailey or Polygonum ×bohemicum (J. Chrtek & Chrtkovß) Zika & Jacobson [cuspidatum ×sachalinense] Family: Polygonaceae Synonyms for Fallopia japonica: Pleuropterus cuspidatus (Sieb. & Zucc.) Moldenke, P. zuccarinii (Small) Small, Polygonum cuspidatum Sieb. & Zucc. var. compactum (Hook. f.) Bailey, P. zuccarinii Small, Reynoutria japonica Houtt. Other common names: Japanese bamboo, fleeceflower, Mexican bamboo Synonyms for Fallopia sachalinensis: Reynoutria sachalinensis (F. Schmidt ex Maxim.) Nakai, Tiniaria sachalinensis (F. Schmidt) Janchen Other common names: none Synonyms for Fallopia x bohemica: none Other common names: none Invasiveness Rank: 87 The invasiveness rank is calculated based on a species’ ecological impacts, biological attributes, distribution, and response to control measures. The ranks are scaled from 0 to 100, with 0 representing a plant that poses no threat to native ecosystems and 100 representing a plant that poses a major threat to native ecosystems. Description Japanese knotweed is a perennial plant that grows from long, creeping rhizomes. Rhizomes are thick, extensive, and 5 to 6 meters long. They store large quantities of carbohydrates. Stems are stout, hollow reddish-brown, swollen at the nodes, and 1 ¼ to 2 ¾ meters tall. Twigs often zigzag slightly from node to node. Leaves are alternate, 5 to 15 cm long, and broadly ovate with more or less truncate bases and acuminate tips. They have short petioles. Plants are dioecious, with male and female flowers on separate plants. Inflorescences are many-flowered, branched, open, and lax. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Asclepias Syriaca L.) After a Single Herbicide Treatment in Natural Open Sand Grasslands László Bakacsy* & István Bagi
www.nature.com/scientificreports OPEN Survival and regeneration ability of clonal common milkweed (Asclepias syriaca L.) after a single herbicide treatment in natural open sand grasslands László Bakacsy* & István Bagi Invasive species are a major threat to biodiversity, human health, and economies worldwide. Clonal growth is a common ability of most invasive plants. The clonal common milkweed Asclepias syriaca L. is the most widespread invasive species in Pannonic sand grasslands. Despite of being an invader in disturbed semi-natural vegetation, this plant prefers agricultural felds or plantations. Herbicide treatment could be one of the most cost-efective and efcient methods for controlling the extended stands of milkweed in both agricultural and protected areas. The invasion of milkweed stand was monitored from 2011 to 2017 in a strictly protected UNESCO biosphere reserve in Hungary, and a single herbicide treatment was applied in May 2014. This single treatment was successful only in a short-term but not in a long-term period, as the number of milkweed shoots decreased following herbicide treatment. The herbicide translocation by rhizomatic roots induced the damage of dormant bud banks. The surviving buds developing shoots, growth of the milkweed stand showed a slow regeneration for a longer-term period. We concluded that the successful control of milkweed after herbicide treatment depends on repeated management of treated areas to suppress further spreading during subsequent seasons. Currently, invasive species are a major threat to biodiversity, human health, and economies 1–4. It has been esti- mated that the fght against invasive species and the damage caused by them in European Union accounts for a minimum of 9.6–12.7 billion euros annually, and this amount is expected to rise to 20 billion euros annually1,5–7. -
Amorpha Canescens Pursh Leadplant
leadplant, Page 1 Amorpha canescens Pursh leadplant State Distribution Best Survey Period Photo by Susan R. Crispin Jan Feb Mar Apr May Jun Jul Aug Sept Oct Nov Dec Status: State special concern the Mississippi valley through Arkansas to Texas and in the western Great Plains from Montana south Global and state rank: G5/S3 through Wyoming and Colorado to New Mexico. It is considered rare in Arkansas and Wyoming and is known Other common names: lead-plant, downy indigobush only from historical records in Montana and Ontario (NatureServe 2006). Family: Fabaceae (pea family); also known as the Leguminosae. State distribution: Of Michigan’s more than 50 occurrences of this prairie species, the vast majority of Synonym: Amorpha brachycarpa E.J. Palmer sites are concentrated in southwest Lower Michigan, with Kalamazoo, St. Joseph, and Cass counties alone Taxonomy: The Fabaceae is divided into three well accounting for more than 40 of these records. Single known and distinct subfamilies, the Mimosoideae, outlying occurrences have been documented in the Caesalpinioideae, and Papilionoideae, which are last two decades from prairie remnants in Oakland and frequently recognized at the rank of family (the Livingston counties in southeast Michigan. Mimosaceae, Caesalpiniaceae, and Papilionaceae or Fabaceae, respectively). Of the three subfamilies, Recognition: Leadplant is an erect, simple to sparsely Amorpha is placed within the Papilionoideae (Voss branching shrub ranging up to ca. 1 m in height, 1985). Sparsely hairy plants of leadplant with greener characterized by its pale to grayish color derived from leaves have been segregated variously as A. canescens a close pubescence of whitish hairs that cover the plant var. -
Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S. -
Characteristics That Make the Fallopia Genus (Polygonaceae) Highly Invasive
Ecological Questions 16/2012: 23 – 27 DOI: 10.2478/v10090-012-0002-6 Characteristics that make the Fallopia genus (Polygonaceae) highly invasive Justyna Sołtysiak, Teresa Brej Department of Botany and Plant Ecology, Wrocław University of Environmental and Life Sciences, pl. Grunwaldzki 24a, 50–363 Wrocław, Poland e-mail: [email protected] Abstract. Representatives of the Fallopia genus: Fallopia japonica, Fallopia sachalinensis and Fallopia × bohemica are known as successful invaders, wide spread throughout Europe and North America. This paper focuses on the invasive Fallopia complex and presents some features (a wide ecological amplitude, high competition abilities, sexual reproduction by hybridization) responsible for the fact that all species of the Fallopia genus are aggressive and noxious invaders. Key words: plant invasion, Fallopia japonica, Fallopia sachalinensis, Fallopia × bohemica. 1. Introduction cies of exotic plants have been introduced as a crop and have escaped to become established in natural ecosystems Biological invasions belong to the main problems of con- (Pimentel et al. 2007). temporary ecology and they are considered as a signifi- Recent research were dedicate to invasive species, de- cant component of global changes, connected with human spite that fact scientist still try to find the answer for the activity (Vitousek et al. 1997; Vilá et al. 2007; McKinney question: what characteristics make them invasive? (Rej- 2006). mánek 1995). The major point of the biological invasions was the The article is dedicated to the Fallopia genus, whose discovery of America by Christopher Columbus in 1492, some species are known as successful invaders, wide which has facilitated exchange of goods between new and spread in Europe and North America. -
Fallopia Japonica – Japanese Knotweed
Fallopia japonica – Japanese knotweed Japanese knotweed, sometimes referred to What is it? as donkey rhubarb for its sour red spring shoots, is a perennial plant in the Buckwheat family (Polygonaceae). It has large broad green leaves; tall, thick, sectioned and somewhat reddish zigzagging stems; and racemes of small papery flowers in summer. Photo by Liz West 2007 Other scientific names (synonyms) for Japanese knotweed are Reynoutria japonica and Polygonum cuspidatum. When does it grow? Shoots emerge from rhizomes (modified underground stems) from late March to mid-April. A spring freeze or deep frost can top kill new growth, but new shoots readily crop up from the hardy rootstalks. Growth continues rapidly once the weather begins to warm reaching heights up to 10 feet or greater by summer. R. Buczynski 2020 4.15.2020 Where is it from? Japanese knotweed is native to eastern Asia and was introduced to the United Kingdom in the 1800’s as a vigorous garden ornamental. Before becoming illegal to plant in England it was horticulturally introduced from the UK to the United States. Where is it now? Japanese knotweed has been reported extensively in the Northeastern U. S. and is currently present in all three counties (Hunterdon, Morris, and Somerset) within the upper Raritan watershed where it continues to spread into moist disturbed areas along waterways. Photo by Roger Kidd © Why is it invasive? Although knotweed can spread by seed, it is most effective at spreading underground via rhizomes that extend outward as well as downward, producing new shoots up to 70 feet away. If detached from the plant, small fragments of rhizome can survive and produce new plants wherever they land. -
Biology and Control of the Invasive Fallopia Taxa
Preface This thesis was written at the Norwegian University of Life Sciences, Department of Plant Sciences (IPV). Lab and greenhouse/garden experiments were carried out at Bioforsk Plant Health in Ås. Supervisors of the thesis are Lars Olav Brandsæter (Associate Professor at NMBU and researcher in weed science at Bioforsk Plant Health, Ås) and Helge Sjursen, (researcher in weed science at Bioforsk Plant Health, Ås). Experiment 1 was made possible through generous financial support from the Norwegian Public Roads Administration. 1 Acknowledgements My greatest thanks go to my supervisors, Lars Olav Brandsæter and Helge Sjursen, for all help, steady guidance and invaluable encouragement during the work with this thesis. Thank you for an educational and enjoyable time as your student, which has increased my interest in weed biology! A great thank also to May Bente Brurberg and Abdelhameed Elameen for all help and guidance on the genetic part of this study, and for reading through my thesis, providing valuable comments. A great thank to Even Sannes Riiser for all help with the barcoding experiment, and to Grete Lund for good and patient teaching in molecular methods. Thank you all for introducing me to the interesting field of genetics and for sharing your expertise and experience. I am greatly thankful to John P. Bailey at the University of Leicester, UK, for providing the control sample of Fallopia japonica used in the genetic analyses, for kindly taking the time to look at my herbarium specimens, and for helpful and inspiring email communication about Fallopia. I would also like to thank Marit Helgheim and Kjell Wernhus for their contributions on the fieldwork, Inger S. -
The Japanese Knotweed Invasion Viewed As a Vast Unintentional Hybridisation Experiment
Heredity (2013) 110, 105–110 & 2013 Macmillan Publishers Limited All rights reserved 0018-067X/13 www.nature.com/hdy ORIGINAL ARTICLE The Japanese knotweed invasion viewed as a vast unintentional hybridisation experiment J Bailey Chromosome counts of plants grown from open-pollinated seed from Japanese knotweed around the world have revealed the presence of extensive hybridisation with both native and other introduced taxa. These hybrids fit into three categories: inter- and intraspecific hybrids involving the taxa of Fallopia section Reynoutria (giant knotweeds), hybrids between Japanese knotweed and F. baldschuanica (Regel) Holub and hybrids between Japanese knotweed and the Australasian endemics of the genus Muehlenbeckia. In this minireview, the viability of the different classes of hybrid and the potential threats they pose are discussed in the context of recent examples of allopolyploid speciation, which generally involve hybridisation between a native and an alien species. Such wide hybridisations also challenge accepted taxonomic classifications. Japanese knotweed s.l. provides a fascinating example of the interplay between ploidy level, hybridisation and alien plant invasion. The octoploid (2n ¼ 88) Fallopia japonica var. japonica (Houtt.) Ronse Decraene is a single female clone throughout much of its adventive range, and provides an ideal system for investigating the potential for wide hybridisation. Heredity (2013) 110, 105–110; doi:10.1038/hdy.2012.98; published online 5 December 2012 Keywords: Fallopia; gynodioecy; polyploidy; invasive alien plant INTRODUCTION conveniently referred to as Japanese knotweed s.l.Theseareallgiant Although the threat to biodiversity posed by exotic invasive species rhizomatous herbs originating from Asia, they are gynodioecious, has long been recognised, less attention has been paid to the role of with hermaphrodite and male-sterile (female) individuals. -
Japanese Knotweed Invasion of the Clones
24_Gillies_Japanese_24.qxd 6/4/10 8:44 PM Page 133 RESEARCH ESSAY Japanese Knotweed: Invasion of the Clones? Sharon L. Gillies University of the Fraser Valley Introduction ave you ever seen headlines like this one? “Watch for flying carp” from the KEY CONCEPTS Toronto Sun, May 24, 2009. Because of amazing photos of Asian carp flying Hthrough the air and YouTube videos of people fishing being struck by fish in ■ Comparing genome their boats, this highly visible invasive species is hard to miss. Other introduced species sequences provides clues are not so noticeable, and some invasive plants have beautiful flowers that we admire. to evolution and High-profile or almost invisible, introduced species are a major threat to biodiversity. development. Many introduced species do not succeed in new environments. Others, however, are ■ Speciation can take place highly successful, and without predators or diseases, they can spread rapidly and disrupt with or without natural communities. geographic separation. Since the introduction of Japanese knotweed (Fallopia japonica) to North America ■ Human activities threaten about a century ago, it has gone from being a prize-winning horticulture plant to being Earth’s biodiversity. labelled one of the world’s top 10 invasive species. In England, Japanese knotweed is sterile and is considered a single, large female clone. In terms of biomass, it is the largest individ- ual female on Earth. With each new plant genetically identical to its mother, it spreads by fragmentation (small pieces breaking off and starting new plants). Evidence indicates that in other parts of Europe and North America, in the absence of male partners of their own species, female Japanese knotweed plants are mating with males from other species. -
Assessing the Potential Distribution of Invasive Alien Species Amorpha
A peer-reviewed open-access journal Nature ConservationAssessing 30: 41–67the potential (2018) distribution of invasive alien species Amorpha fruticosa... 41 doi: 10.3897/natureconservation.30.27627 RESEARCH ARTICLE http://natureconservation.pensoft.net Launched to accelerate biodiversity conservation Assessing the potential distribution of invasive alien species Amorpha fruticosa (Mill.) in the Mureş Floodplain Natural Park (Romania) using GIS and logistic regression Gheorghe Kucsicsa1, Ines Grigorescu1, Monica Dumitraşcu1, Mihai Doroftei2, Mihaela Năstase3, Gabriel Herlo4 1 Institute of Geography, Romanian Academy, 12 D. Racoviţă Street, sect. 2, 023993, Bucharest, Romania 2 Danube Delta National Institute, 165 Babadag Street, 820112, Tulcea, Romania 3 National Forest Ad- ministration, Protected Areas Department, 9A Petricani Street, sect. 2, Bucharest, Romania 4 National Forest Administration, Mureş Floodplain Natural Park Administration, Pădurea Ceala FN, Arad, Romania Corresponding author: Monica Dumitraşcu ([email protected]) Academic editor: Maurizio Pinna | Received 19 June 2018 | Accepted 2 October 2018 | Published 24 October 2018 http://zoobank.org/EF484149-F35A-4B0F-9F8B-4F8164BFF94F Citation: Kucsicsa G, Grigorescu I, Dumitraşcu M, Doroftei M, Năstase M, Herlo G (2018) Assessing the potential distribution of invasive alien species Amorpha fruticosa (Mill.) in the Mureş Floodplain Natural Park (Romania) using GIS and logistic regression. Nature Conservation 30: 41–67. https://doi.org/10.3897/natureconservation.30.27627