Garlon 360 Trial for the Control of Wetland Weeds
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Juncus Pallidus
Juncus pallidus COMMON NAME Giant rush, leafless rush SYNONYMS Juncus macrostigma Colenso FAMILY Juncaceae AUTHORITY Juncus pallidus R.Br. FLORA CATEGORY Vascular – Native ENDEMIC TAXON No ENDEMIC GENUS No ENDEMIC FAMILY No STRUCTURAL CLASS Rushes & Allied Plants NVS CODE JUNPAL Juncus pallidus - last seasons inflorescences, CURRENT CONSERVATION STATUS Oratia Native Plant Nurseries. Photographer: 2012 | Not Threatened Peter de Lange, 3 May 2007, PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened DISTRIBUTION Indigenous. North, South, and Stewart Islands. Present in Australia and naturalised on Norfolk, Lord Howe and the Chatham Islands HABITAT Coastal to lowland. Often in pastures where it can be as major weed. Usually in damp swampy hollows, on the margins of wetlands and lakes, in open shrubland on damp ground, or near saltmarshes in places that can be flooded by King tides. Juncus pallidus close up of fruiting inflorescences, Oratia Native Plant Nurseries. Photographer: Peter de Lange FEATURES Very robust, tall perennial forming dense patches up to 2 m tall. Rhizome 5-10 mm diameter, horizontal. Flowering stems 1-2 m tall, 3-8 mm diameter, erect, very rarely drooping, smooth, slightly glossy, light green or glaucous, soft, pith continuous; leaves absent; basal sheathing bracts numerous, lower ones shorter, upper ones larger, loosely sheathing, very obtuse with a long, hair-like mucro, light green, light brown or pinkish brown, Inflorescence apparently lateral, many-flowered, usually contracted into a dense head > 15 mm wide, or effuse with long stout, rigid branchlets. Flowers 2.3-3.0 mm long, clustered at branchlet apices, or evenly spaced along branchlets, on stout pedicels or almost sessile; tepals pale green, occasionally tinged with pink, maturing light brown, the outer rigid, the inner soft and membranous, almost colourless. -
Otanewainuku ED (Report Prepared on 13 August 2013)
1 NZFRI collection wish list for Otanewainuku ED (Report prepared on 13 August 2013) Fern Ally Isolepis cernua Lycopodiaceae Isolepis inundata Lycopodium fastigiatum Isolepis marginata Lycopodium scariosum Isolepis pottsii Psilotaceae Isolepis prolifera Tmesipteris lanceolata Lepidosperma australe Lepidosperma laterale Gymnosperm Schoenoplectus pungens Cupressaceae Schoenoplectus tabernaemontani Chamaecyparis lawsoniana Schoenus apogon Cupressus macrocarpa Schoenus tendo Pinaceae Uncinia filiformis Pinus contorta Uncinia gracilenta Pinus patula Uncinia rupestris Pinus pinaster Uncinia scabra Pinus ponderosa Hemerocallidaceae Pinus radiata Dianella nigra Pinus strobus Phormium cookianum subsp. hookeri Podocarpaceae Phormium tenax Podocarpus totara var. totara Iridaceae Prumnopitys taxifolia Crocosmia xcrocosmiiflora Libertia grandiflora Monocotyledon Libertia ixioides Agapanthaceae Watsonia bulbillifera Agapanthus praecox Juncaceae Alliaceae Juncus articulatus Allium triquetrum Juncus australis Araceae Juncus conglomeratus Alocasia brisbanensis Juncus distegus Arum italicum Juncus edgariae Lemna minor Juncus effusus var. effusus Zantedeschia aethiopica Juncus sarophorus Arecaceae Juncus tenuis var. tenuis Rhopalostylis sapida Luzula congesta Asparagaceae Luzula multiflora Asparagus aethiopicus Luzula picta var. limosa Asparagus asparagoides Orchidaceae Cordyline australis x banksii Acianthus sinclairii Cordyline banksii x pumilio Aporostylis bifolia Asteliaceae Corunastylis nuda Collospermum microspermum Diplodium alobulum Commelinaceae -
Coastal Planting Guide 1 for Detailed Information Are Very Dynamic Places with No Two Being Exactly Alike
Arno Gasteiger - Coastal wetland Whakanewha Regional Park Coastal wetlands, saltmarshes & estuaries We can all be part of protecting, restoring and connecting Auckland's biodiversity. Coastal wetlands, saltmarshes & estuaries This factsheet provides a basic planting guide for coastal wetlands, estuaries and saltmarshes which are found in the dynamic saline zone between the land and the sea. It provides a coastal planting supplement to the Auckland Council’s Riparian Zone Management Guidelines which focuses on freshwater and inland environments, and to the Wetland planting guide factsheet. In the Auckland region, wetlands typically form on the edges of streams and lakes and in estuaries or damp, boggy places where water collects. Estuaries form where rivers and streams flow into the sea. They are partly enclosed by land and contain a mixture of fresh and salt water. Salt water moves in and out of estuaries with each tide. Special places The region’s coastal wetlands, saltmarshes and estuaries are important and special places. These areas contain a diverse range of flora and fauna and offer significant habitat for many rare and threatened species. Wetlands and estuaries form a buffer zone between land and sea, protecting the land from erosion and also acting as a filter, by trapping sediment and pollutants from land run off, that would otherwise flow into coastal waters. Coastal wetlands & estuaries in the Auckland region Coastal wetland types in the Auckland region include: Mangrove swamps – mangroves are found in the shallow areas of many of the region’s estuaries and in coastal wetland areas. Saltmarsh – dominated by sea rush, oioi and saltmarsh ribbon wood. -
Jervis Bay Territory Page 1 of 50 21-Jan-11 Species List for NRM Region (Blank), Jervis Bay Territory
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
The Smut Fungi (Ustilaginomycetes) of Restionaceae S. Lat
MYCOLOGIA BALCANICA 3: 19–46 (2006) 19 Th e smut fungi (Ustilaginomycetes) of Restionaceae s. lat. Kálmán Vánky Herbarium Ustilaginales Vánky (H.U.V.), Gabriel-Biel-Str. 5, D-72076 Tübingen, Germany (e-mail: [email protected]) Received 2 October 2005 / Accepted 25 October 2005 Abstract. Smut fungi of Restionaceae s. lat. were studied. Th ey are classifi ed into two genera, Restiosporium and Websdanea. Problems of species delimitation in these smuts are discussed. In addition to the nine known smut fungi, thirteen new species are described and illustrated: Restiosporium anarthriae, R. apodasmiae, R. chaetanthi, R. desmocladii, R. eurychordae, R. fl exuosum, R. hypolaenae, R. lepyrodiae, R. pallentis, R. patei, R. proliferum, R. spathacei, and R. sphacelatum. Key words: new species, Restionaceae s. lat., Restiosporium, smut fungi, taxonomy, Websdanea Introduction and stained in 1 % aqueous uranyl acetate for 1 h in the dark. After fi ve washes in distilled water, the material was Th e monocotyledonous Restionaceae is a remarkable family dehydrated in acetone series, embedded in Spurr’s plastic, of Southern Hemisphere, evergreen, rush-like plants. Th ey and sectioned with a diamond knife. Semi-thin sections are concentrated mainly in SW Africa and in SW Australia. were stained with new fuchsin and crystal violet, mounted Th e c. 320 species of African Restionaceae, in 19 genera, were in ‘Entellan’ and studied in a light microscope. revised by Linder (1985, 1991). Th e 170 species of Australian Spore ball and spore morphology was studied using Restionaceae s. lat. were published by Meney & Pate (1999) a light microscope (LM) with an oil immersion lens at a in a beautifully illustrated monograph. -
Low Risk Aquarium and Pond Plants
Plant Identification Guide Low-risk aquarium and pond plants Planting these in your pond or aquarium is environmentally-friendly. Glossostigma elatinoides, image © Sonia Frimmel. One of the biggest threats to New Zealand’s waterbodies is the establishment and proliferation of weeds. The majority of New Zealand’s current aquatic weeds started out as aquarium and pond plants. To reduce the occurrence of new weeds becoming established in waterbodies this guide has been prepared to encourage the use of aquarium and pond plants that pose minimal risk to waterbodies. Guide prepared by Dr John Clayton, Paula Reeves, Paul Champion and Tracey Edwards, National Centre of Aquatic Biodiversity and Biosecurity, NIWA with funding from the Department of Conservation. The guides will be updated on a regular basis and will be available on the NIWA website: www.niwa.co.nz/ncabb/tools. Key to plant life-forms Sprawling marginal plants. Grow across the ground and out over water. Pond plants Short turf-like plants. Grow in shallow water on the edges of ponds and foreground of aquariums. Includes very small plants (up to 2-3 cm in height). Most species can grow both submerged (usually more erect) and emergent. Pond and aquarium plants Tall emergent plants. Can grow in water depths up to 2 m deep depending on the species. Usually tall reed-like plants but sometimes with broad leaves. Ideal for deeper ponds. Pond plants Free floating plants. These plants grow on the water surface and are not anchored to banks or bottom substrates. Pond and aquarium plants Floating-leaved plants. Water lily-type plants. -
New Zealand Rushes: Juncus Factsheets
New Zealand Rushes: Juncus factsheets K. Bodmin, P. Champion, T. James and T. Burton www.niwa.co.nz Acknowledgements: Our thanks to all those who contributed photographs, images or assisted in the formulation of the factsheets, particularly Aarti Wadhwa (graphics) at NIWA. This project was funded by TFBIS, the Terrestrial and Freshwater Biodiversity information System (TFBIS) Programme. TFBIS is funded by the Government to help New Zealand achieve the goals of the New Zealand Biodiversity Strategy and is administered by the Department of Conservation (DOC). All photographs are by Trevor James (AgResearch), Kerry A. Bodmin or Paul D. Rushes: Champion (NIWA) unless otherwise stated. Additional images and photographs were kindly provided by Allan Herbarium; Auckland Herbarium; Larry Allain (USGS, Wetland and Aquatic Research Center); Forest and Kim Starr; Donald Cameron (Go Botany Juncus website); and Tasmanian Herbarium (Threatened Species Section, Department of Primary Industries, Parks, Water and Environment, Tasmania). factsheets © 2015 - NIWA. All rights Reserved. Cite as: Bodmin KA, Champion PD, James T & Burton T (2015) New Zealand Rushes: Juncus factsheets. NIWA, Hamilton. Introduction Rushes (family Juncaceae) are a common component of New Zealand wetland vegetation and species within this family appear very similar. With over 50 species, Juncus are the largest component of the New Zealand rushes and are notoriously difficult for amateurs and professionals alike to identify to species level. This key and accompanying factsheets have been developed to enable users with a diverse range of botanical expertise to identify Juncus to species level. The best time for collection, survey or identification is usually from December to April as mature fruiting material is required to distinguish between species. -
Impact of Sea Level Rise on Coastal Natural Values in Tasmania
Impact of sea level rise on coastal natural values in Tasmania JUNE 2016 Department of Primary Industries, Parks, Water and Environment Acknowledgements Thanks to the support we received in particular from Clarissa Murphy who gave six months as a volunteer in the first phase of the sea level rise risk assessment work. We also had considerable technical input from a range of people on various aspects of the work, including Hans and Annie Wapstra, Richard Schahinger, Tim Rudman, John Church, and Anni McCuaig. We acknowledge the hard work over a number of years from the Sea Level Rise Impacts Working Group: Oberon Carter, Louise Gilfedder, Felicity Faulkner, Lynne Sparrow (DPIPWE), Eric Woehler (BirdLife Tasmania) and Chris Sharples (University of Tasmania). This report was compiled by Oberon Carter, Felicity Faulkner, Louise Gilfedder and Peter Voller from the Natural Values Conservation Branch. Citation DPIPWE (2016) Impact of sea level rise on coastal natural values in Tasmania. Natural and Cultural Heritage Division, Department of Primary Industries, Parks, Water and Environment, Hobart. www.dpipwe.tas.gov.au ISBN: 978-1-74380-009-6 Cover View to Mount Cameron West by Oberon Carter. Pied Oystercatcher by Mick Brown. The Pied Oystercatcher is considered to have a very high exposure to sea level rise under both a national assessment and Tasmanian assessment. Its preferred habitat is mudflats, sandbanks and sandy ocean beaches, all vulnerable to inundation and erosion. Round-leaved Pigface (Disphyma australe) in flower in saltmarsh at Lauderdale by Iona Mitchell. Three saltmarsh communities are associated with the coastal zone and are considered at risk from sea level rise. -
Marginal Evidence for Taro Production in Northern New Zealand
LETTER REPLY TO BARBER: Marginal evidence for taro production in northern LETTER New Zealand between 1200 and 1500 CE Matthew Prebblea,1, Atholl J. Andersona, Paul Augustinusb, Joshua Emmittc, Stewart J. Fallond, Louise L. Fureye, Simon J. Holdawayc, Alex Jorgensenc, Thegn N. Ladefogedc,f, Peter J. Matthewsg, Jean-Yves Meyerh, Rebecca Phillippsc, Rod Wallacec, and Nicholas Porchi We welcome Barber’s (1) comments and are grateful for not meet widely accepted criteria for high-precision the opportunity to respond. Our study of wetland taro dating, as they contain mixed carbon sources (9). (Colocasia esculenta) gardens during the initial coloni- 3) Description of crop ecosystems: Ancient crop ecosys- zation period (ICP) (1200 to 1500 CE) in New Zealand tems cannot be described without comprehensive did not overlook the evidence from the Aupouri Penin- analyses of biological remains from archaeological sula (2–4). We agree that gardens were probably estab- contexts. At Polynesian arrival, the Motutangi wet- lished on mainland New Zealand, within the climate lands were dominated by the large-statured conifer envelope shown in figure 1 of our paper (4), but in areas Dacrydium cupressinum, requiring repeated firing to that lacked large-statured forests at Polynesian arrival. establish gardens, and Restionaceae (3), most likely However, the fossil evidence from Motutangi does not Apodasmia similis, a rush which dominates the mar- meet the 3 criteria for defining ICP taro gardens met in gins of regularly flooded estuaries or lakes and out- our study of Ahuahu and subtropical French Polynesia: competes other plants in nutrient-poor soils (10). This densely spreading rush likely posed difficulties for 1) Reliable fossil proxies: We identify pollen, the crop cultivation, although taro may have been com- most reliable fossil proxy for taro (5), but also clus- petitive if grown in clumps over multiple sea- ters of small globular orbicular starch grains inside sons. -
Patterns of Flammability Across the Vascular Plant Phylogeny, with Special Emphasis on the Genus Dracophyllum
Lincoln University Digital Thesis Copyright Statement The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). This thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: you will use the copy only for the purposes of research or private study you will recognise the author's right to be identified as the author of the thesis and due acknowledgement will be made to the author where appropriate you will obtain the author's permission before publishing any material from the thesis. Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy at Lincoln University by Xinglei Cui Lincoln University 2020 Abstract of a thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy. Abstract Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum by Xinglei Cui Fire has been part of the environment for the entire history of terrestrial plants and is a common disturbance agent in many ecosystems across the world. Fire has a significant role in influencing the structure, pattern and function of many ecosystems. Plant flammability, which is the ability of a plant to burn and sustain a flame, is an important driver of fire in terrestrial ecosystems and thus has a fundamental role in ecosystem dynamics and species evolution. However, the factors that have influenced the evolution of flammability remain unclear. -
Travis Report
Travis Marsh:- invertebrate inventory and analysis R.P. Macfarlane Buzzuniversal 43 Amyes Road, Hornby Christchurch B.H. Patrick P.O. Box 6202, Great King Street, Otago Museum, Dunedin P.M. Johns Zoology Department, Canterbury University, Christchurch C.J. Vink Entomology and animal ecology Department, Lincoln University, Lincoln May 1998 Page CONTENTS 1 SUMMARY 2 INTRODUCTION 5 The marsh 5 Lowland invertebrate communities 7 Terrestrial invertebrate survey objectives 9 METHODS 10 Sampling procedure and site features 10 Fauna investigation and identification 13 RESULTS AND DISCUSSION 14 Invertebrate biodiversity and mobility 14 Habitat and ecological relationships 16 Foliage, seed herbivores and their parasites 17 Insects on invasive weeds of Travis Marsh 20 Parasites and their distribution on the marsh 21 Flower visitors 21 The predators 22 Ground, litter and tree trunk dwellers 23 Drainage, seepage and wet bare spot inhabitants 24 Cattle and pukeko dung 25 Pukeko diet and feeding 25 Skinks 26 Sampling methods and imput needs for an invertebrate community study 26 ANALYSIS AND CONCLUSIONS 27 Biodiversity 27 Localized species loss 28 Characteristic marsh and native woodland species 29 Research and education prospects 29 Recreational value and restoration potential 30 ACKNOWLEDGMENTS 31 REFERENCES 32 Table 1 Biodiversity and habitat surveys of New Zealand grasslands to marshes (arranged by geographic and habitat proximity to Travis Marsh) 8 Table 2 Invertebrate collection:- duration, composition and habitats sampled 13 Table 3 Comparison of relative abundance of insect groups from a malaise trap at shrub/tree and the tall marsh plant sites 16 Appendix 1 Invertebrates found at Travis Marsh (467 insect species, 88 ‘introduced’ species) 39 Appendix 2 Site, plant and method details for the survey 59 Appendix 3 Selected invertebrate species: simplified keys, informal family characters and some reasons to consider species are undescribed 60 Figure 1 Travis Marsh with location of sample sites 11 Figure 2 Vegetation and east ditch boundary of the Long I. -
Wenderholm 2015/16 Seed Collection
Wenderholm 2015/16 Seed Collection Table of Contents Introduction 1 Apodasmia similis 2 Carex virgata 3 Coprosma macrocarpa subsp. macrocarpa 4 Coprosma robusta 5 Cordyline australis 6 Cyperus ustulatus 7 Dacrycarpus dacrydioides 8 Hebe stricta var. stricta 9 Juncus kraussii subsp. australiensis 10 Kunzea robusta 11 Leptospermum scoparium var. scoparium 12 Melicytus ramiflorus 13 Metrosideros excelsa 14 Phormium tenax 15 Plagianthus divaricatus 16 Glossary 17 Made on the New Zealand Plant Conservation Network website – www.nzpcn.org.nz Copyright All images used in this book remain copyright of the named photographer. Any reproduction, retransmission, republication, or other use of all or part of this book is expressly prohibited, unless prior written permission has been granted by the New Zealand Plant Conservation Network ([email protected]). All other rights reserved. © 2015 New Zealand Plant Conservation Network Introduction About the Network This book was compiled from information stored on the The Network has more than 800 members worldwide and is website of the New Zealand Plant Conservation Network New Zealand's largest nongovernmental organisation solely (www.nzpcn.org.nz). devoted to the protection and restoration of New Zealand's indigenous plant life. This website was established in 2003 as a repository for information about New Zealand's threatened vascular The vision of the New Zealand Plant Conservation Network is plants. Since then it has grown into a national database of that 'no indigenous species of plant will become extinct nor be information about all plants in the New Zealand botanic placed at risk of extinction as a result of human action or region including both native and naturalised vascular indifference, and that the rich, diverse and unique plant life of plants, threatened mosses, liverworts and fungi.