Fireweed Risk Assessment
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Current and Potential Distribution of Senecio Madagascariensis Poir
Japanese Society of Grassland Science Japanese Society of Grassland Science ISSN1744-6961 ORIGINAL ARTICLE Current and potential distribution of Senecio madagascariensis Poir. (fireweed), an invasive alien plant in Japan Michio Tsutsumi National Agricultural Research Center for Western Region, Ohda, Shimane, Japan Keywords Abstract Invasive alien plant; macroclimatic environment; Maxent; potential distribution; The short-lived perennial (sometimes annual) plant, Senecio madagascariensis Senecio madagascariensis. Poir. (fireweed) is native to South Africa and Madagascar. This plant is an invasive weed becoming naturalized over a wide range of the world, and has caused agri- Correspondence cultural damage mainly due to its toxicity to livestock. In Japan, fireweed was first Michio Tsutsumi, National Agricultural found in 1976, and has been spreading throughout the country. In this study, the Research Center for Western Region, Ohda, Shimane 694-0013, Japan. current distribution of fireweed in Japan was investigated. Using a maximum Email: [email protected] entropy ecological niche modeling algorithm, the relationship between the distri- bution records of fireweed and climatic variables was modeled, and the potential Received 10 February 2011; distribution of fireweed was predicted. Many growing sites of fireweed have been Accepted 19 April 2011. observed on the Pacific coast and Seto Inland Sea coast. The northern and south- ern ends of the current distribution were the Pacific coast of southern Tohoku doi: 10.1111/j.1744-697X.2011.00222.x (36.9172°N, 140.8613°E) and southern Kyushu (31.5654°N, 130.3438°E), respec- tively. The results of modeling showed that mean temperature in the warmest quarter was the most influential predictor, and suggested that geographical distri- bution of fireweed in Japan is restricted mainly by temperature, not by precipita- tion. -
Senecio Madagascariensis
Senecio madagascariensis Madagascar ragwort, Madagascar fireweed, variable groundsel Senecio madagascariensis Poiret Family: Asteraceae Description: Low, upright, branched herb to 2 ft tall. Leaves smooth, narrow, up to 5 inches long by 1 inch wide, alternate, entire or lobed, margins serrated. Flow- ers profusely, 0.75 inches diameter, daisy-like flowers, each with 13 petals, disc and petals bright yellow, ma- tures into thistle ball which quickly blows away in the wind. Each flower is capable of producing 150 long- lived seeds and each plant can produce 30,000 seeds(67). Senecio is derived from the Latin senex, old man, for the white thistles(70); madagascariensis, of Madagas- car(69). The reason for the common name “fireweed” in Australia is uncertain. It has been speculated that it was due to its rapid spread, or the fact that it colonizes burnt- Environmental impact: Ragwort is toxic (pyrro- out areas, or that it causes spontaneous combustion in lizidine alkaloids) to cattle and horses, and although alfalfa hay, or because of its bright yellow color(67). The sheep and goats are somewhat tolerant, they can become Weed Science Society of America, to bring more con- ill or be killed by grazing too much fireweed(71). Although sistency to weed names, has adopted “Madagscar rag- fireweed poisoning of livestock in Hawai‘i is not appar- wort” as the common name for this weed. “Fireweed” ent so far, because cattle and horses will not normally is a very frequently used common name and is generi- graze the weed, it may become a problem in times of cally meaningless. -
Sterol Addition During Pollen Collection by Bees
Sterol addition during pollen collection by bees: another possible strategy to balance nutrient deficiencies? Maryse Vanderplanck, Pierre-Laurent Zerck, Georges Lognay, Denis Michez To cite this version: Maryse Vanderplanck, Pierre-Laurent Zerck, Georges Lognay, Denis Michez. Sterol addition during pollen collection by bees: another possible strategy to balance nutrient deficiencies?. Apidologie, 2020, 51 (5), pp.826-843. 10.1007/s13592-020-00764-3. hal-02784696 HAL Id: hal-02784696 https://hal.archives-ouvertes.fr/hal-02784696 Submitted on 3 May 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Apidologie (2020) 51:826–843 Original article * INRAE, DIB and Springer-Verlag France SAS, part of Springer Nature, 2020 DOI: 10.1007/s13592-020-00764-3 Sterol addition during pollen collection by bees: another possible strategy to balance nutrient deficiencies? 1,2 1 3 1 Maryse VANDERPLANCK , Pierre-Laurent ZERCK , Georges LOGNAY , Denis MICHEZ 1Laboratory of Zoology, Research Institute for Biosciences, University of Mons, 20 Place du Parc, 7000, Mons, Belgium 2CNRS, UMR 8198 - Evo-Eco-Paleo, Univ. Lille, F-59000, Lille, France 3Analytical Chemistry, Agro Bio Chem Department, Gembloux Agro-Bio Tech University of Liège, 2 Passage des Déportés, 5030, Gembloux, Belgium Received 10 July 2019 – Revised2March2020– Accepted 30 March 2020 Abstract – Sterols are essential nutrients for bees which are thought to obtain them exclusively from pollen. -
TAXON:Pluchea Carolinensis SCORE:16.0 RATING:High Risk
TAXON: Pluchea carolinensis SCORE: 16.0 RATING: High Risk Taxon: Pluchea carolinensis Family: Asteraceae Common Name(s): cattletongue Synonym(s): Conyza carolinensis Jacq. (basionym) cure-for-all Pluchea odorata auct. nonn. shrubby fleabane Pluchea symphytifolia auct. sourbush stinking fleabane sweet-scent tabat-diable wild tobacco Assessor: Chuck Chimera Status: Assessor Approved End Date: 11 May 2015 WRA Score: 16.0 Designation: H(Hawai'i) Rating: High Risk Keywords: Weedy Shrub, Aromatic, Hybridizes, Thicket-forming, Wind-dispersed Qsn # Question Answer Option Answer 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? 103 Does the species have weedy races? Species suited to tropical or subtropical climate(s) - If 201 island is primarily wet habitat, then substitute "wet (0-low; 1-intermediate; 2-high) (See Appendix 2) High tropical" for "tropical or subtropical" 202 Quality of climate match data (0-low; 1-intermediate; 2-high) (See Appendix 2) High 203 Broad climate suitability (environmental versatility) y=1, n=0 n Native or naturalized in regions with tropical or 204 y=1, n=0 y subtropical climates Does the species have a history of repeated introductions 205 y=-2, ?=-1, n=0 y outside its natural range? 301 Naturalized beyond native range y = 1*multiplier (see Appendix 2), n= question 205 y 302 Garden/amenity/disturbance weed 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see Appendix 2) y 304 Environmental weed n=0, y = 2*multiplier (see Appendix 2) y 305 Congeneric -
Fireweed Report
Fireweed in Australia Directions for Future Research 2 Professor Brian Sindel School of Environmental and Rural Science University of New England Armidale, New South Wales 2351 Phone 02 6773 3747 Fax 02 6773 3238 Email [email protected] January 2009 Report for the Bega Valley Fireweed Association PO Box 79 Bega NSW 2550 http://thebegavalley.org.au/fireweed.html Fireweed in Australia – Directions for Future Research 3 Contents Executive Summary 5 Why this Report? 7 What do we Know? 10 Identity 10 Botanical name 10 Common name 10 Recent taxonomical revisions 11 Worldwide distribution 12 Africa 12 South America 13 Japan 13 Hawaii 13 Spread and distribution in Australia 13 Recent spread 14 Future spread 15 Factors affecting further spread 17 Frost 17 Climate change 17 Other factors 17 Habitat 17 Climatic requirements 18 Soils 18 Plant associations 18 Growth and development 18 Perennation 18 Physiology 20 Phenology 20 Reproduction 20 Floral biology and breeding system 20 Genetic variation 21 Seed production and dispersal 22 Physiology of seeds and germination 23 Vegetative reproduction 25 Hybridization 25 Population dynamics 25 Impact 26 Invasiveness and competition 26 Economic and social impact 28 Toxicity 28 To livestock 28 To humans 30 Legislation 30 Fireweed in Australia – Directions for Future Research 4 Fireweed management 31 Herbicides 31 Pasture management 32 Grazing 33 Hand weeding 34 Mowing 34 Cultivation 34 Natural enemies 34 Biological control 35 What Research is Underway? 37 What Research is Needed? 38 Biological control 38 Is fireweed just a management issue? 38 Cost effectiveness of biocontrol 38 Pinpointing the area of origin of fireweed 39 Host specificity 39 Potential collaboration 42 First stage 42 Ecology 43 Impact 43 Better management 44 Conclusion 46 Acknowledgments 47 Acronyms 48 References 49 Appendix 1 – About the Author 58 Appendix 2 – Description of Fireweed 59 Description of S. -
“Study of the Effects of an Artificial Cut on the Invasive Plant S. Ineaquidens”
UNIVERSITAT POLITÈCNICA DE VALÈNCIA E S C O L A POLITÈCNICA SUPERIOR D E G A N D I A Grau en Ciències Ambientals “Study of the effects of an artificial cut on the invasive plant S. Ineaquidens” TREBALL FINAL DE GRAU Autor/a: Marc Fuster Adrover Tutor/s: Prof. Dr. Martin Diekmann Prof. Dra. Maria Pilar Donat Torres GANDIA, 2016 2 3 I ABSTRACT .......................................................................................................... 5 1 INTRODUCTION ................................................................................................. 6 2 MATERIAL AND METHODS ............................................................................. 9 2.1 STUDY SITE AND PLANT SAMPLING ........................................................................ 9 2.2 PLANT TREATMENT AND ANALYSIS ...................................................................... 10 2.3 STATISTICAL ANALYSIS ........................................................................................ 11 3 RESULTS .......................................................................................................... 12 3.1 CONSEQUENCES OF CUT ON INDIVIDUAL SURVIVAL OF S. INEAQUIDENS ........... 12 3.2 CONSEQUENCES OF CUT ON GROWTH OF S. INEAQUIDENS ................................ 13 3.3 CONSEQUENCES OF CUT ON FLOWER PRODUCTION OF S. INEAQUIDENS .......... 17 4 DISCUSSION .................................................................................................... 19 4.1 METHODOLOGY ................................................................................................... -
Data Sheet For
Web version 2006-02-01 - doc 05-11836 EPPO data sheet on Invasive Plants Senecio inaequidens Identity Scientific name: Senecio inaequidens De Candolle Synonyms: Senecio burchellii De Candolle, Senecio Taxonomic position: Asteraceae. Common names: Narrow-leaved ragwort, South African ragwort (English), séneçon du Cap (French), schmalblättriges Greiskraut, schmalblättriges Kreuzkraut, südafrikanisches Greiskraut (German), senecione sudafricano (Italian). EPPO code: SENIQ Notes on taxonomy and nomenclature: Senecio inaequidens DC. (Asteraceae) is a perennial plant originally growing in South Africa which was unintentionally and independently introduced into several sites in Europe from 1889 onwards. The identity of the plant in Europe has long been in doubt; it has been called S. harveianus Mac Owan and quite erroneously S. lautus Solander ex Willd (Tutin et al., 1976). In fact, Senecio inaequidens De Candolle, Senecio madagascariensis Poiret and Senecio harveianus Mac Owan are three Senecio species growing in South Africa frequently confused by the botanists. Molecular studies have shown that South African S. madagascariensis was more closely related to South African S. inaequidens than to Madagascan S. madagascariensis. However chromosome counts revealed that individuals of S. inaequidens are tetraploids in Europe whereas Australian individuals of S. madagascariensis, which have a South African origin, are diploids. The tetraploid form is very aggressive (Lafuma et al., 2003). A comparison of some South African populations of the three species and a study on ploidy level was conducted. It showed that S. inaequidens, S. madagascariensis and S. harveianus are the same species and that polyploidisation of S. inaequidens occurred in South Africa and seeds introduced in Europe probably came from tetraploid populations of the Lesotho area (Lafuma et al., 2002). -
Senecio Madagascariensis Poir.) in the Hawaiian Islands As Inferred from Phylogenetic Analysis Johannes J
Diversity and Distributions, (Diversity Distrib.) (2006) 12, 694–702 Blackwell Publishing Ltd BIODIVERSITY Resolving the native provenance of RESEARCH invasive fireweed (Senecio madagascariensis Poir.) in the Hawaiian Islands as inferred from phylogenetic analysis Johannes J. Le Roux1*, Ania M. Wieczorek1, Mohsen M. Ramadan2 and Carol T. Tran1 1Department of Tropical Plant and Soil Sciences, ABSTRACT University of Hawaii at Manoa, 3190 Maile Accurate identification of weedy species is critical to the success of biological control Way, St. John 102, Honolulu, Hawaii 96822, USA, and 2Division of Plant Industry, Hawaii programs seeking host-specific control agents. Phylogenetic relationships based on Department of Agriculture, 1428 South King internal transcribed spacer region (ITS1, ITS2) DNA sequence data were used to Street, Honolulu, Hawaii 96814, USA elucidate the most likely origin and taxonomic placement of Senecio madagascariensis Poir. (fireweed; Asteraceae) in the Hawaiian archipelago. Putative S. madagascarien- sis populations from Madagascar, South Africa, Swaziland, and Hawaii were included in the analysis. Different phylogenetic models (maximum parsimony and maximum likelihood) were congruent in suggesting that Hawaiian fireweed is most closely related to populations from the KwaZulu-Natal region in South Africa. Phylogenetic divergence and morphological data (achene characteristics) suggest that the S. madagascariensis complex is in need of revised alpha-level taxonomy. Taxonomic identity of invasive fireweed in Hawaii is important for finding effective biological control agents as native range populations constitute different biotypic variants across a wide geographical area. Based on our phylogenetic results, research directed at biological control of Hawaiian infestations should focus on areas in the KwaZulu- Natal region in South Africa where host-specific natural enemies are most likely to be found. -
Senecio Inaequidens DC
CCCOMMUNAUTÉ FFFRANÇAISE DE BBBELGIQUE AAACADEMIE UUUNIVERSITAIRE WWWALLONIE ---E-EEEUROPE FFFACULTE UUUNIVERSITAIRE DES SSSCIENCES AAAGRONOMIQUES DE GGGEMBLOUX SSSOURCES DE VARIATION PHÉNOTYPIQUE DES TRATRAITSITS DDD’’’HISTOIRE DE VIE D ’’’UNE ESPÈCE INVASIVE ,,, SSSENECIO INAEQUIDENS DC. (A(A(A STERACEAE ).).). Arnaud MMMONTY EEESSAI PRÉSENTÉ EN VUE DE L '''OBTENTION DU GRADE DDEE DOCTEUR EN SCIENCESCIENCESS AGRONOMIQUES ET INGINGÉNIERIEÉNIERIE BIOLOGIQUE Promoteur : Pr. Grégory MMMAHY Année 2009 CCCOMMUNAUTÉ FFFRANÇAISE DE BBBELGIQUE AAACADEMIE UUUNIVERSITAIRE WWWALLONIE ---E-EEEUROPE FFFACULTE UUUNIVERSITAIRE DES SSSCIENCES AAAGRONOMIQUES DE GGGEMBLOUX SSSOURCES DE VARIATION PHÉNOTYPIQUE DES TRATRAITSITS DDD’’’HISTOIRE DE VIE D ’’’UNE ESPÈCE INVASIVE ,,, SSSENECIO INAEQUIDENS DC. (A(A(A STERACEAE ).).). Arnaud MMMONTY EEESSAI PRÉSENTÉ EN VUE DE L '''OBTENTION DU GRADE DDEE DOCTEUR EN SCIENCESCIENCESS AGRONOMIQUES ET INGINGÉNIERIEÉNIERIE BIOLOGIQUE Promoteur : Pr. Grégory MMMAHY Année 2009 Monty Arnaud. (2009). Sources de variation phénotypique des traits d’histoire de vie d’une espèce invasive, Senecio inaequidens DC. (Asteraceae)(thèse de doctorat). Gembloux, Faculté Universitaire des Sciences Agronomiques. 18 p., 1 fig., 1 tableau, 7 articles. Résumé L’importance des différentes sources de variation phénotypique que sont l’adaptation, la plasticité phénotypique, les effets maternels environnementaux, le niveau de ploïdie et la dérive génétique, a été analysée pour différents traits d’histoire de vie, au sein de l’aire colonisée par une espèce végétale invasive. A cette fin, plusieurs expériences en jardins communs ont été installées, dont deux en transplantations réciproques. Les populations considérées étaient localisées en Belgique, en France, ainsi que dans l’aire d’indigénat de l’espèce. Senecio inaequidens DC. (Asteraceae), l’espèce étudiée dans ce travail, est une plante d’origine africaine accidentellement introduite en Europe par le commerce lainier, vers la fin du 19 ème siècle. -
Plants in Urban Environments in Relation to Global Change Drivers at Different Scales
Plants in urban environments in relation to global change drivers at different scales Dissertation Zur Erlangung der Würde des Doktors der Naturwissenschaften des Fachbereichs Biologie der Fakultät für Mathematik, Informatik und Naturwissenschaften der Universität Hamburg vorgelegt von Katharina Johanna Schmidt aus Heidelberg Hamburg 2014 TABLE OF CONTENTS List of figures V List of tables VII Summary 1 Zusammenfassung 5 1 Introduction 11 1.1 Urbanisation 11 1.2 Environmental conditions in urban areas and urbanisation gradients 12 1.3 History of urban ecology 13 1.4 Urban areas and vegetation 14 1.5 Climate change and biodiversity 19 1.6 Hamburg as a case study 23 1.7 Aims and outline of the thesis 27 2 Effects of urban structure on plant species richness in a large European city 31 2.1 Introduction 31 2.2 Methods 33 2.3 Results 38 2.4 Discussion 43 2.5 Acknowledgements 45 3 Plant species distribution clearly reflects the structure of Hamburg (Germany) on a meso-scale 47 3.1 Introduction 47 3.2 Methods 49 3.3 Results 53 3.4 Discussion 58 3.5 Acknowledgements 60 3.6 Appendix 61 4 Floristic mapping data as a proxy for the mean urban heat island 65 4.1 Introduction 65 4.2 Data and Methods 67 4.3 Results and Discussion 73 4.4 Conclusions and Outlook 79 4.5 Acknowledgements 80 5 Plant species diversity in select habitats along an urbanisation gradient 83 5.1 Introduction 83 5.2 Methods 84 5.3 Results 85 5.4 Discussion and Outlook 87 6 Biotic interactions of Senecio inaequidens DC. -
The Phylogenetic Structure of Plant-Pollinator Networks Increases with Habitat Size and Isolation
S1 Supporting Information The phylogenetic structure of plant-pollinator networks increases with habitat size and isolation Marcelo A. Aizen, Gabriela Gleiser, Malena Sabatino, Luis J. Gilarranz, Jordi Bascompte, and Miguel Verdú Content Supporting Materials and Methods Tables S1-S14 Figures S1-S5 S2 Supporting Materials and Methods Landscape’s human transformation The fertile Austral Pampas’ region, where the study sierras are located, was effectively colonized by criollos of Spanish descent between 1820 and 1830, and the land divided among the first “estancieros”, whose main activity was cattle-raising. The transformation from pasture to cropland on the plains surrounding the sierras occurred at the end of the 19th century associated with the onset of the big European immigration to Argentina (Barsky & Gelman 2001). As it happened across the Pampas, a relatively diverse agriculture dominated by wheat was replaced, starting in the late seventies, by one monopolized by soybean (Aizen et al. 2009). Today the sierras emerge as true islands of diversity amidst a relatively uniform agriculture matrix (Fig. 1). Threshold distance Functional connectivity depends on the dispersal capacity of individuals. Thus, it is difficult to determine a priori the threshold distance below which two given habitat patches are expected to be "connected" based solely on theoretical expectations, particularly for community attributes. An empirical approach frequently used in landscape ecological studies is to identify the threshold distance that maximizes the variance explained by the correlation between a given connectivity metric and a population/community attribute (e.g. Steffan-Dewenter et al. 2002). We followed this approach by estimating the relation between phylogenetic signals in interactions and estimates of patch betweenness centrality for each of the 12 focal sierras (Table S1), considering threshold distances between 10 and 20 km (Table S2). -
The Risk of Injurious and Toxic Plants Growing in Kindergartens Vanesa Pérez Cuadra, Viviana Cambi, María De Los Ángeles Rueda, and Melina Calfuán
Consequences of the Loss of Traditional Knowledge: The risk of injurious and toxic plants growing in kindergartens Vanesa Pérez Cuadra, Viviana Cambi, María de los Ángeles Rueda, and Melina Calfuán Education Abstract The plant kingdom is a producer of poisons from a vari- ered an option for people with poor education or low eco- ety of toxic species. Nevertheless prevention of plant poi- nomic status or simply as a religious superstition (Rates sonings in Argentina is disregarded. As children are more 2001). affected, an evaluation of the dangerous plants present in kindergartens, and about the knowledge of teachers in Man has always been attracted to plants whether for their charge about them, has been conducted. Floristic inven- beauty or economic use (source of food, fibers, dyes, etc.) tories and semi-structured interviews with teachers were but the idea that they might be harmful for health is ac- carried out at 85 institutions of Bahía Blanca City. A total tually uncommon (Turner & Szcawinski 1991, Wagstaff of 303 species were identified, from which 208 are consid- 2008). However, poisonings by plants in humans repre- ered to be harmless, 66 moderately and 29 highly harm- sent a significant percentage of toxicological consulta- ful. Of the moderately harmful, 54% produce phytodema- tions (Córdoba et al. 2003, Nelson et al. 2007). titis, and among the highly dangerous those with alkaloids and cyanogenic compounds predominate. The number of Although most plants do not have any known toxins, there dangerous plants species present in each institution var- is a variety of species with positive toxicological studies ies from none to 45.