Sydney-Wide Ludwigia Regional Plan 08-13
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Ludwigia Spp
A WEED REPORT from the book Weed Control in Natural Areas in the Western United States This WEED REPORT does not constitute a formal recommendation. When using herbicides always read the label, and when in doubt consult your farm advisor or county agent. This WEED REPORT is an excerpt from the book Weed Control in Natural Areas in the Western United States and is available wholesale through the UC Weed Research & Information Center (wric.ucdavis.edu) or retail through the Western Society of Weed Science (wsweedscience.org) or the California Invasive Species Council (cal-ipc.org). Ludwigia spp. Waterprimroses Family: Onagraceae Range: Primarily in the coastal states, Washington, Oregon and California; creeping waterprimrose is also found in Arizona and New Mexico. Habitat: Slow-flowing rivers, lake and reservoir margins, and in the shallow waters of canals and floodplains. Origin: Most species are native to South America. L. peploides ssp. peploides is native to California, Arizona, New Mexico, Ludwigia peploides Texas, and Louisiana; ssp. glabrescens (Kuntze) Raven is native to the central and eastern U.S.; and ssp. montevidensis (Spreng.) Raven is introduced from southern South America. L. peploides is sometimes sold as an aquarium or pond ornamental. Impacts: Dense stands degrade natural communities, reduce water quality and floodwater retention, and prevent effective mosquito control. Plants can develop a tangled mat of stems that can reduce water flow in irrigation channels and drainage ditches. Western states listed as Noxious Weed: L. grandiflora, Washington California Invasive Plant Council (Cal-IPC) Inventory: L. hexapetala, High Invasiveness (Alert); L. peploides, High Invasiveness Waterprimroses are floating to emergent perennials with stems to 10 ft long. -
Report of a Pest Risk Analysis For: Ludwigia Grandiflora
EUROPEAN AND MEDITERRANEAN PLANT PROTECTION ORGANIZATION ORGANISATION EUROPEENNE ET MEDITERRANEENNE POUR LA PROTECTION DES PLANTES 11-17142 Report of a Pest Risk Analysis for: Ludwigia grandiflora This summary presents the main features of a pest risk analysis which has been conducted on the pest, according to EPPO Decision support scheme for quarantine pests. Pest: Ludwigia grandiflora PRA area: The PRA area is the EPPO region (see map www.eppo.org). Assessors: A Draft PRA had been prepared by Mr Guillaume Fried, and the Expert Working Group was attended by the following experts: Mr Mustafa Selçuk Basaran, Plant Protection Central Research Institute, Turkey Mr Alain Dutartre, CEMAGREF, France Mr Guillaume Fried, LNPV Station de Montpellier, France Mr Jonathan Newman, Waterland Management Ltd, United Kingdom Mr Uwe Starfinger, Julius Kühn Institute, Germany Mr Johan van Valkenburg, Plant Protection Service, The Netherlands EPPO Secretariat: Ms Sarah Brunel Comments were received from Ms Iris Stiers, Vrije Universiteit Brussel, Belgium, and Mr Andreas Hussner, University of Duesseldorf, Germany. Peer review has been undertaken by Ms Schrader, Julius Kühn Institute, Germany. Date: Expert working group 06-2010, core member consultation 06-2011 STAGE 1: INITIATION Reason for doing PRA: L. grandiflora is widespread and invasive in the South and West of France but its distribution is still very limited in the North and East of France, as well as in Belgium, Germany, Ireland, Italy, the Netherlands, Spain and the UK where invasion is at an early stage. The species could spread to further EPPO countries and have negative impacts on agriculture and the environment. Taxonomic position of Kingdom: Plantae pest: Class: Magnoliopsida (Dicotyledons) Subclass: Rosidae Order: Myrtales Family: Onagraceae Ludwigia grandiflora ressembles and is often confused with L. -
An Assessment of Exotic Species in the Tonle Sap Biosphere Reserve
AN ASSESSMENT OF EXOTIC SPECIES IN THE TONLE SAP BIOSPHERE RESERVE AND ASSOCIATED THREATS TO BIODIVERSITY A RESOURCE DOCUMENT FOR THE MANAGEMENT OF INVASIVE ALIEN SPECIES December 2006 Robert van Zalinge (compiler) This publication is a technical output of the UNDP/GEF-funded Tonle Sap Conservation Project Executive Summary Introduction This report is mainly a literature review. It attempts to put together all the available information from recent biological surveys, and environmental and resource use studies in the Tonle Sap Biosphere Reserve (TSBR) in order to assess the status of exotic species and report any information on their abundance, distribution and impact. For those exotic species found in the TSBR, it is examined whether they can be termed as being an invasive alien species (IAS). IAS are exotic species that pose a threat to native ecosystems, economies and/or human health. It is widely believed that IAS are the second most significant threat to biodiversity worldwide, following habitat destruction. In recognition of the threat posed by IAS the Convention on Biological Diversity puts forward the following strategy to all parties in Article 8h: “each contracting party shall as far as possible and as appropriate: prevent the introduction of, control, or eradicate those alien species which threaten ecosystems, habitats or species”. The National Assembly of Cambodia ratified the Convention on Biological Diversity in 1995. After reviewing the status of exotic species in the Tonle Sap from the literature, as well as the results from a survey based on questionnaires distributed among local communities, the main issues are discussed, possible strategies to combat the spread of alien species that are potentially invasive are examined, and recommendations are made to facilitate the implementation of a strategy towards reducing the impact of these species on the TSBR ecosystem. -
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. -
Ludwigia Grandiflora (Large-Flower Primrose-Willow) ERSS
Large-flower Primrose-willow (Ludwigia grandiflora) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, May 2012 Revised, March 2018 Web Version, 2/1/2019 Photo: O. Pichard. Licensed under Creative Commons (CC-BY-SA-3.0). Available: https://commons.wikimedia.org/wiki/File:Ludwigia_grandiflora_saint-mathurin-sur- loire_49_10082007_4.JPG. (March 2018). 1 Native Range and Status in the United States Native Range From CABI (2018): “L. grandiflora is native to the Americas, ranging from the Rio La Plata in Argentina north to the south/southeastern USA. In the USA, its range is primarily along the Atlantic coast and through the Gulf Coastal Plain (southeastern New York through Florida, westward to Texas) (McGregor et al., 1996).” From NatureServe Explorer (2018): “Global range includes two disjunct areas, one in southern Brazil, Bolivia, northeastern Argentina, Uruguay, and Paraguay (also locally in Guatemala), and the second (with relevance here) in the southeastern United States coastal plains of southern South Carolina, Georgia, northern Florida, and Louisiana, west to central Texas; and once in southwest Missouri (Zardini et al., 1991; Crow and Hellquist, 2000a).” “There is some uncertainty over the native range of Ludwigia grandiflora.” The USDA Natural Resources Conservation Service (2018) website reports all occurrences in the contiguous United States are introductions. Status in the United States From NatureServe Explorer (2018): “This species has expanded rapidly in the past in the United States beyond its original early invasion into the Pacific Northwest and the American southeast. It is now found in more than 20 states with recent expansion continuing, though not as rapidly because a significant portion of its potential range has already been filled. -
Recent Distribution and Phytosociological Affiliation of Ludwigia Palustris in Slovakia
Acta Societatis Botanicorum Poloniae DOI: 10.5586/asbp.3544 ORIGINAL RESEARCH PAPER Publication history Received: 2016-02-28 Accepted: 2017-03-08 Recent distribution and phytosociological Published: 2017-03-31 affiliation of Ludwigia palustris in Slovakia Handling editor Joanna Zalewska-Gałosz, Faculty of Biology and Earth Sciences of the Jagiellonian University, Daniel Dítě1, Pavol Eliáš Jr.2*, Zuzana Dítě1, Andrea Šimková3 Poland 1 Plant Science and Biodiversity Center, Institute of Botany, Slovak Academy of Sciences, Dúbravská cesta 9, 845 23 Bratislava, Slovakia Authors’ contributions 2 Slovak University of Agriculture, A. Hlinku 2, 949 76 Nitra, Slovakia DD: idea of the study; DD, ZD: 3 Administration of Latorica Protected Landscape Area, Záborského 1760/1, 075 01 Trebišov, writing the first draft of the Slovakia manuscript; PE: revision of the manuscript, map and table * Corresponding author. Email: [email protected] creating; AŠ: comments to the manuscript; all the authors: field study, relevés sampling Abstract Funding Ludwigia palustris has always been a very rare species in Central Europe. In Slo- The research was partially vakia, its occurrence remained unconfirmed for over 60 years and it was therefore funded by the projects VEGA 1/0083/16 and VEGA 2/0040/17. considered extinct. The paper reports its rediscovery on two sites in SE Slovakia. Both localities were found in the Latorica River catchment area in 2015 when per- Competing interests sistent summer droughts enabled the development of natural mudflat vegetation No competing interests have in the dried oxbows. Confirmation of this historic site indicates the long-term been declared. survival ability of the species. -
Folivory and Disease Occurrence on Ludwigia Hexapetala in Guntersville Reservoir, Alabama
J. Aquat. Plant Manage. 55: 19–25 Folivory and disease occurrence on Ludwigia hexapetala in Guntersville Reservoir, Alabama NATHAN E. HARMS, JUDY F. SHEARER, AND MICHAEL J. GRODOWITZ* ABSTRACT southeastern United States, with disjunct populations in California and Oregon (Grewell et al. 2016). Invasive We report leaf feeding, disease occurrence, and associ- populations also exist outside the United States in France, ated indigenous herbivore/fungal pathogen communities Belgium, Italy, Spain, Greece, the United Kingdom, and The on the introduced wetland species Ludwigia hexapetala at Netherlands (Dandelot et al. 2005, Thouvenot et al. 2013). Guntersville Reservoir, AL. Plant populations were sam- Closely related Ludwigia are difficult to distinguish mor- pled on three dates from May to September 2014. A phologically, and conflicting diagnostic characters have complex of indigenous herbivore and fungal taxa, mostly been presented by various authors (Nesom and Kartesz known from other Ludwigia spp., resulted in peak feeding 2000). Ludwigia hexapetala is decaploid (2n ¼ 80; Zardini et al. and disease occurrence on 88% and 92% of sampled 1991), a characteristic that may contribute to relative leaves, respectively. Herbivore damage declined over the invasiveness over other Ludwigia spp. (Pandit et al. 2011, growing season from 78 to 21% of sampled leaves, and Grewell et al. 2016). disease symptom occurrence increased from 0 to 80%. Management of L. hexapetala in the United States is a Total leaf damage (percent leaf area) from both herbivory concern as the number and distribution of infestations and disease was determined by software image analyses of increase. Ludwigia hexapetala causes economic damage floating and aerial leaves and reached 14% total reduction through disruption of flood control, irrigation water in photosynthetic tissues by September 2014. -
Ludwigia ID Guide
A handful of primary features are useful for distinguishing water primrose (Ludwigia) from other plants. Understand what to look for, such as leaf arrangement and number of petals. Pairing morphological features with growth habit in the field quickly narrows down the thirty-odd species of water primrose in Florida to the handful most commonly found in the lakes, ponds, rivers and canals typically frequented by aquatic managers. 1 This genus of plants was named after a German botanist may not have been happy over the Latinization of his name. Florida has about 30 species. Habitat serves as general indicator of species. 2 Ludwigia peruviana is our most commonly seen species. Demonstrating little preference for an aquatic habitat, it forms tall thickets along roadside ditch banks and upper shorelines. It recurs perennially from thick, woody stem bases. Its tough stems and rough, hairy leaves afford a level of upland tolerance to this non-native, invasive species. 3 Most pertinent to aquatic managers in Florida are the emergent aquatics. 4 Stems are what gives these emergent species of aquatic habitats a special punch. They are reservoirs of energy used in maintaining, expanding, and recurring populations. With our emergent Ludwigia, stems are the most important plant feature in management. Fibrous roots acquire nutrients and help bind the submersed and floating stems into dense mats that provide support for emergent stems. 5 Special aquatic adaptations for oxygenation in an anaerobic environment. It is common for aquatic Ludwigia species to display multiple shades of green and red. 6 Apply these three initial steps to eliminate species and to arrive at the emergent aquatic Ludwigia in Florida. -
Common Name: Anglestem Primrose-Willow Scientific Name: Ludwigia Leptocarpa Family: Myrtales Order: Onagraceae Wetland Plant
Common Name: Anglestem Primrose-willow Scientific Name: Ludwigia leptocarpa Family: Myrtales Order: Onagraceae Wetland Plant Status: Obligatory Ecology & Description Anglestem primrose-willow is an upright, branched perennial plant that can grow up to 1 meter tall. Its stem is a stout, 4-angled stem that can be green, brown, or tan. The leaves are alternate, lanceolate, and up to 14 cm long and 2.5 cm wide. Yellow flowers that are 6-12 mm long and 4-6 mm wide are produced from May to October. The flowers have 4-7 petals and have to bracts. Fruit and seeds develop November through March. Fruits are a 4- sided, tubular capsule that is 2 cm long and 2-4.5 cm wide. The seeds are spread when the plant is shaken by the wind. Habitat Anglestem primrose-willow inhabits wet soils in new forests, right-of-ways, and older forest openings. Distribution It grows naturally as far north as Pennsylvania, as far east as Texas, and as far south as Puerto Rico. Native/Invasive Status This species is native to the Gulf Coastal Plain and Southeastern United States, as well as Puerto Rico Wildlife Uses Anglestem primrose-willow a forage used by white-tailed deer (Odocoileus virginianus). Wood ducks (Aix sponsa) have also used this plant as a minor food source in the fall. The nutritional value of anglestem primrose-willow ranges from moderate to poor. Management & Control Techniques In many places anglestem primrose-willow is thought of as a weed. If you want to remove it from a pond, remove the seed heads and burn them. -
Appendix A. Plant Species Known to Occur at Canaveral National Seashore
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science Vegetation Community Monitoring at Canaveral National Seashore, 2009 Natural Resource Data Series NPS/SECN/NRDS—2012/256 ON THE COVER Pitted stripeseed (Piriqueta cistoides ssp. caroliniana) Photograph by Sarah L. Corbett. Vegetation Community Monitoring at Canaveral National Seashore, 2009 Natural Resource Report NPS/SECN/NRDS—2012/256 Michael W. Byrne and Sarah L. Corbett USDI National Park Service Southeast Coast Inventory and Monitoring Network Cumberland Island National Seashore 101 Wheeler Street Saint Marys, Georgia, 31558 and Joseph C. DeVivo USDI National Park Service Southeast Coast Inventory and Monitoring Network University of Georgia 160 Phoenix Road, Phillips Lab Athens, Georgia, 30605 March 2012 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado publishes a range of reports that address natural resource topics of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Data Series is intended for the timely release of basic data sets and data summaries. Care has been taken to assure accuracy of raw data values, but a thorough analysis and interpretation of the data has not been completed. Consequently, the initial analyses of data in this report are provisional and subject to change. All manuscripts in the series receive the appropriate level of peer review to ensure that the information is scientifically credible, technically accurate, appropriately written for the intended audience, and designed and published in a professional manner. -
Biological and Host Range Characteristics of Lysathia Flavipes
insects Article Biological and Host Range Characteristics of Lysathia flavipes (Coleoptera: Chrysomelidae), a Candidate Biological Control Agent of Invasive Ludwigia spp. (Onagraceae) in the USA Angelica M. Reddy 1,* , Paul D. Pratt 1, Brenda J. Grewell 2 , Nathan E. Harms 3, Ximena Cibils-Stewart 4, Guillermo Cabrera Walsh 5 and Ana Faltlhauser 5,6 1 USDA-ARS, Invasive Species and Pollinator Health Research Unit, Western Regional Research Center, 800 Buchanan St., Albany, CA 94710, USA; [email protected] 2 USDA-ARS, Invasive Species and Pollinator Health Research Unit, University of California Davis, Department of Plant Sciences Mail Stop 4, One Shields Ave, Davis, CA 95616, USA; [email protected] 3 US Army Engineer Research and Development Center (ERDC), Aquatic Ecology and Invasive Species Branch, 3909 Halls Ferry Rd, Vicksburg, MS 39180, USA; [email protected] 4 Instituto Nacional de Investigación Agropecuaria (INIA), Estación Experimental INIA La Estanzuela, Ruta 50 Km 11, Colonia del Sacramento, Colonia, Uruguay; [email protected] 5 Fundación para el Estudio de Especies Invasivas (FuEDEI), Simón Bolívar 1559, Hurlingham (CP1686), Buenos Aires B1686EFA, Argentina; [email protected] (G.C.W.); [email protected] (A.F.) 6 Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, Ciudad Autónoma de Buenos Aires C1425FQB, Argentina * Correspondence: [email protected] Citation: Reddy, A.M.; Pratt, P.D.; Grewell, B.J.; Harms, N.E.; Simple Summary: Exotic water primroses (Ludwigia spp.) are aggressive plant invaders in aquatic Cibils-Stewart, X.; Cabrera Walsh, G.; Faltlhauser, A. Biological and Host ecosystems worldwide. Management of exotic Ludwigia spp. -
Floristic Composition of the South-Central Florida Dry Prairie Landscape Steve L
Floristic Composition of the South-Central Florida Dry Prairie Landscape Steve L. Orzell Avon Park Air Force Range, 29 South Blvd., Avon Park Air Force Range, FL 33825-5700 [email protected] Edwin L. Bridges Botanical and Ecological Consultant, 7752 Holly Tree Place NW, Bremerton, WA 98312-1063 [email protected] ABSTRACT Floristic composition of the Florida dry prairie landscape was compiled from 291 sites in nine south-central peninsular counties. Floristic lists were based upon field inventory and compilation from reliable sources to- taling 11,250 site and community type-specific observations and were analyzed by region (Kissimmee River, Desoto/Glades “Big Prairie,” and Myakka). The known vascular flora consists of 658 vascular plant taxa, rep- resenting 317 genera and 115 families. Families with the highest number of species are Poaceae (103), Asteraceae (78), Cyperaceae (76), Fabaceae (23), Scrophulariaceae (20), and Orchidaceae (18). The most diverse genera are Rhynchospora (29), Dichanthelium (17), Ludwigia (13), Xyris (12), and Andropogon (11). Of this flora 24 taxa are endemic to central or southern peninsular Florida, primarily within the pine savanna- flatwood/dry prairie landscape, and 41 taxa are of Floridian biotic affinity. Although most species are not re- gionally specific, a few (Carphephorus carnosus, Ctenium aromaticum, and Liatris spicata) appear to be ab- sent from the Myakka prairie region, while Marshallia tenuifolia appears to be absent from both the Desoto/ Glades and Myakka prairie regions. Within the dry prairie landscape Hypericum edisonianum is restricted to the Desoto/Glades region. A few other species somewhat differentiate between prairie regions; however, most occur in other habitats in the counties where they are absent or nearly absent from dry prairie.