Appendix 1-2 USACE Invasive Plant ID on Army Lands, Base Year 2011
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Flora and Fauna
ENVIRONMENTAL ASSESSMENT Volume 2 Technical Papers MUNMORAH GAS TURBINE FACILITY MUNMORAH POWER STATION.indd 3 21/12/05 2:27:29 PM Contents Technical Papers (Volume 2) Technical Paper No.1 Flora and Fauna Assessment Technical Paper No.2 Heritage Assessment Technical Paper No.3 Noise Assessment Technical Paper No.4 Air Quality Impact Assessment Technical Paper No 5 Photochemical Pollution Assessment Technical Paper No 6 Preliminary Hazard Analysis FLORA AND FAUNA ASSESSMENT TECHNICAL PAPER DIVIDERS.indd 30 121/12/05 3:44:33 PM Technical Paper 1 Flora and Fauna Assessment of Munmorah Gas Turbine Facility December 2005 Delta Electricity Parsons Brinckerhoff Australia Pty Limited ACN 078 004 798 and Parsons Brinckerhoff International (Australia) Pty Limited ACN 006 475 056 trading as Parsons Brinckerhoff ABN 84 797 323 433 Level 27 Ernst & Young Centre 680 George Street Sydney NSW 2000 GPO Box 5394 Australia Telephone +61 2 9272 5100 Facsimile +61 2 9272 5101 Email [email protected] ABN 84 797 323 433 NCSI Certified Quality System ISO 9001 2116541A Parsons Brinckerhoff supports the Environment by PR_2467.doc printing on 100per cent A4 recycled paper ©Parsons Brinckerhoff Australia Pty Limited and Parsons Brinckerhoff International (Australia) Pty Limited trading as Parsons Brinckerhoff (“PB”). [2005] Copyright in the drawings, information and data recorded in this document (“the information”) is the property of PB. This document and the information are solely for the use of the authorised recipient and this document may not be used, copied or reproduced in whole or part for any purpose other than that for which it was supplied by PB. -
New England Peppermint (Eucalyptus Nova-Anglica) Grassy
Advice to the Minister for Sustainability, Environment, Water, Population and Communities from the Threatened Species Scientific Committee on an Amendment to the List of Threatened Ecological Communities under the Environment Protection and Biodiversity Conservation Act 1999 (EPBC Act) 1. Name of the ecological community New England Peppermint (Eucalyptus nova-anglica) Grassy Woodlands This advice follows the assessment of two public nominations to list the ‘New England Peppermint (Eucalyptus nova-anglica) Woodlands on Sediment on the Northern Tablelands’ and the ‘New England Peppermint (Eucalyptus nova-anglica) Woodlands on Basalt on the Northern Tablelands’ as threatened ecological communities under the EPBC Act. The Threatened Species Scientific Committee (the Committee) recommends that the national ecological community be renamed New England Peppermint (Eucalyptus nova-anglica) Grassy Woodlands. The name reflects the fact that the definition of the ecological community has been expanded to include all grassy woodlands dominated or co-dominated by Eucalyptus nova-anglica (New England Peppermint), in New South Wales and Queensland. Also the occurrence of the ecological community extends beyond the New England Tableland Bioregion, into adjacent areas of the New South Wales North Coast and the Nandewar bioregions. Part of the national ecological community is listed as endangered in New South Wales, as ‘New England Peppermint (Eucalyptus nova-anglica) Woodland on Basalts and Sediments in the New England Tableland Bioregion’ (NSW Scientific Committee, 2003); and, as an endangered Regional Ecosystem in Queensland ‘RE 13.3.2 Eucalyptus nova-anglica ± E. dalrympleana subsp. heptantha open-forest or woodland’ (Qld Herbarium, 2009). 2. Public Consultation A technical workshop with experts on the ecological community was held in 2005. -
Supporting Information
Supporting Information Christin et al. 10.1073/pnas.1216777110 SI Materials and Methods blades were then embedded in resin (JB-4; Polysciences), Phylogenetic Inference. A previously published 545-taxa dataset of following the manufacturer’s instructions. Five-micrometer the grasses based on the plastid markers rbcL, ndhF,andtrnK-matK thick cross-sections of the embedded leaf fragments were cut (1) was expanded and used for phylogenetic inference. For species with a microtome and stained with saturated cresyl violet sampled for anatomical cross-sections but not included in the acetate (CVA). Some samples were fixed in formalin-pro- published dataset, the markers ndhF and/or trnK-matK were either pionic acid-alcohol (FPA), embedded in paraffin, sectioned at retrieved from GenBank when available or were newly sequenced 10 μm, and stained with a safranin O-orange G series (11) as from extracted genomic DNA with the method and primers de- described in (12). All slides were made permanent and are scribed previously (1, 2). These new sequences were aligned to the available on request. dataset, excluding the regions that were too variable as described previously (1). The final dataset totaled 604 taxa and was used for Anatomical Measurements. All C3 grasses possess a double BS, with “ phylogenetic inference as implemented in the software Bayesian the outer layer derived from ground meristem to form a paren- ” Evolutionary Analysis by Sampling Trees (BEAST) (3). chyma sheath, and the internal layer derived from the vascular “ ” The phylogenetic tree was inferred under a general time-re- procambium to form a mestome sheath (13). Many C4 grasses versible substitution model with a gamma-shape parameter and also possess these two BS layers, with one of them specialized in “ ” a proportion of invariants (GTR+G+I). -
Topic 27: GRASSES (Poaceae)
Australian Plants Society NORTH SHORE GROUP Ku-ring-gai Wildflower Garden Topic 27: GRASSES (Poaceae) Did you know that, Grass pollen first appeared in fossil record 50 million years ago, at the start of the Eocene period. They are thought to have evolved alongside grazing mammals. Poaceae is one of the most diverse and abundant plant groups. Worldwide it contains 700 genera and 10,000 species. In Australia there are 220 genera and 1,230 species. 30% are introduced. They are adapted to a wide range of habitats from alpine to warm tropical savannah regions where there is plenty of sun, moisture and warmth. The Importance of Grasses They are of great economic importance and have made human civilization possible. It is estimated that grasses supply 60% of the world’s food. All of the cereal grains: wheat, rice, maize, oats, barley, rye, sorghum and millet are grasses. The meat, poultry, dairy and wool growing industries depend on grazing or cereals. Sugar cane and bamboo are grasses. Grasses form the basis of natural ecosystems such as grasslands. Why are grasses so successful? They produce large quantities of seed which are spread by wind, water and animals. Some have hooks, hairs or awns to facilitate this. They can survive adverse conditions by reproducing vegetatively from buds on underground stems. This enables survival from drought and fire. They are wind pollinated and produce large quantities of pollen. The flowers are small, green and inconspicuous as they do not need to attract pollinators. Grasses are Monocotyledons These are herbaceous plants which have one seed leaf (cotyledon), strap-like leaves with parallel veins, a fibrous root system and usually no woody material. -
1 CV: Snow 2018
1 NEIL SNOW, PH.D. Curriculum Vitae CURRENT POSITION Associate Professor of Botany Curator, T.M. Sperry Herbarium Department of Biology, Pittsburg State University Pittsburg, KS 66762 620-235-4424 (phone); 620-235-4194 (fax) http://www.pittstate.edu/department/biology/faculty/neil-snow.dot ADJUNCT APPOINTMENTS Missouri Botanical Garden (Associate Researcher; 1999-present) University of Hawaii-Manoa (Affiliate Graduate Faculty; 2010-2011) Au Sable Institute of Environmental Studies (2006) EDUCATION Ph.D., 1997 (Population and Evolutionary Biology); Washington University in St. Louis Dissertation: “Phylogeny and Systematics of Leptochloa P. Beauv. sensu lato (Poaceae: Chloridoideae)”. Advisor: Dr. Peter H. Raven. M.S., 1988 (Botany); University of Wyoming. Thesis: “Floristics of the Headwaters Region of the Yellowstone River, Wyoming”. Advisor: Dr. Ronald L. Hartman B.S., 1985 (Botany); Colorado State University. Advisor: Dr. Dieter H. Wilken PREVIOUS POSITIONS 2011-2013: Director and Botanist, Montana Natural Heritage Program, Helena, Montana 2007-2011: Research Botanist, Bishop Museum, Honolulu, Hawaii 1998-2007: Assistant then Associate Professor of Biology and Botany, School of Biological Sciences, University of Northern Colorado 2005 (sabbatical). Project Manager and Senior Ecologist, H. T. Harvey & Associates, Fresno, CA 1997-1999: Senior Botanist, Queensland Herbarium, Brisbane, Australia 1990-1997: Doctoral student, Washington University in St. Louis; Missouri Botanical Garden HERBARIUM CURATORIAL EXPERIENCE 2013-current: Director -
Lose the Plot: Cost-Effective Survey of the Peak Range, Central Queensland
Lose the plot: cost-effective survey of the Peak Range, central Queensland. Don W. Butlera and Rod J. Fensham Queensland Herbarium, Environmental Protection Agency, Mt Coot-tha Botanic Gardens, Mt Coot-tha Road, Toowong, QLD, 4066 AUSTRALIA. aCorresponding author, email: [email protected] Abstract: The Peak Range (22˚ 28’ S; 147˚ 53’ E) is an archipelago of rocky peaks set in grassy basalt rolling-plains, east of Clermont in central Queensland. This report describes the flora and vegetation based on surveys of 26 peaks. The survey recorded all plant species encountered on traverses of distinct habitat zones, which included the ‘matrix’ adjacent to each peak. The method involved effort comparable to a general flora survey but provided sufficient information to also describe floristic association among peaks, broad habitat types, and contrast vegetation on the peaks with the surrounding landscape matrix. The flora of the Peak Range includes at least 507 native vascular plant species, representing 84 plant families. Exotic species are relatively few, with 36 species recorded, but can be quite prominent in some situations. The most abundant exotic plants are the grass Melinis repens and the forb Bidens bipinnata. Plant distribution patterns among peaks suggest three primary groups related to position within the range and geology. The Peak Range makes a substantial contribution to the botanical diversity of its region and harbours several endemic plants among a flora clearly distinct from that of the surrounding terrain. The distinctiveness of the range’s flora is due to two habitat components: dry rainforest patches reliant upon fire protection afforded by cliffs and scree, and; rocky summits and hillsides supporting xeric shrublands. -
C4 Photosynthetic Evolution
C4 PHOTOSYNTHETIC EVOLUTION: SUB-TYPES, DIVERSITY, AND FUNCTION WITHIN THE GRASS TRIBE PANICEAE _______________________________________ A Dissertation presented to the Faculty of the Graduate School at the University of Missouri-Columbia _______________________________________________________ In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy _____________________________________________________ by JACOB DANIEL WASHBURN Dr. J. Chris Pires, Dissertation Supervisor MAY 2017 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled: C4 PHOTOSYNTHETIC EVOLUTION: SUB-TYPES, DIVERSITY, AND FUNCTION WITHIN THE GRASS TRIBE PANICEAE Presented by Jacob Daniel Washburn, a candidate for the degree of doctor of philosophy, and hereby certify that, in their opinion, it is worthy of acceptance. _____________________________ Dr. J. Chris Pires _____________________________ Dr. James A. Birchler _____________________________ Dr. Paula McSteen _____________________________ Dr. Gavin Conant ACKNOWLEDGEMENTS I would first like to thank my beautiful wife and sweetheart Melinda for her constant companionship, support, and sacrifice over the past five years. Also my three children: Nathan, Sam, and Emma. The four of you have been, and continue to be my inspiration, and my happiness. I also want to thank my parents, Shelley and Kevin Washburn, who instilled in me a love for learning and for hard work. This degree is for you as well. I also thank my advisor Chris for being the most supportive, helpful, and forward- thinking mentor I have ever had the privilege of associating with. I credit you with the success I have had in grant writing during my Ph.D., and with many of the life skills I have learned. My co-advisor Jim has also been an incredible help. -
2016 Ecological Monitoring Report
2016 Ecological Monitoring Report 2016 Ecological Monitoring Report Bulga Coal Complex Bulga Surface Operations Pty Ltd & Bulga Underground Operations Pty Ltd July 2016 Prepared by Prepared by DnA Environmental July 2016 i 2016 Ecological Monitoring Report Disclaimer This is a report of work carried out by DnA Environmental on behalf of the Bulga Coal Management Pty Ltd and Bulga Underground Operations Pty Ltd, collectively referred to as the Bulga Coal Complex (BCC) and has been prepared according to the brief provided by the client. The information contained herein is complete and correct to the best of my knowledge. The representations, statements, opinions and advice, expressed or implied in this report are produced in good faith but on the basis that DnA Environmental are not liable (whether by reason of negligence, lack of care or otherwise) to any person for any damage or loss whatsoever which has occurred or may occur in relation to that person taking or not taking (as the case may be) action in respect of any or all of the content. Signed: Dr Donna Johnston Restoration Ecologist PhD, B.App.Sc (Hons) MEIANZ Draft submitted: 15th July 2016 Reviewed: 20th December 2016, Tom Scott (Bulga Surface Ops) Final submitted: 21st December 2016 DnA Environmental 417 Mandurama Rd Mandurama NSW 2792 Ph/Fax: (02) 63 675 251 Mobile: 0408 221 922 [email protected] ABN 19 607 392 634 Acknowledgements The field surveys and resultant report were undertaken by and prepared by Dr Donna Johnston and Andrew Johnston from DnA Environmental. Tom Scott (Bulga Open Cut) and Marty Salm (Bulga Underground Operations) provided comments on the report. -
Anatomical Enablers and the Evolution of C4 Photosynthesis in Grasses
Anatomical enablers and the evolution of C4 photosynthesis in grasses Pascal-Antoine Christina, Colin P. Osborneb, David S. Chateleta, J. Travis Columbusc, Guillaume Besnardd, Trevor R. Hodkinsone,f, Laura M. Garrisona, Maria S. Vorontsovag, and Erika J. Edwardsa,1 aDepartment of Ecology and Evolutionary Biology, Brown University, Providence, RI 02912; bDepartment of Animal and Plant Sciences, University of Sheffield, Sheffield S10 2TN, United Kingdom; cRancho Santa Ana Botanic Garden, Claremont Graduate University, Claremont, CA 91711; dUnité Mixte de Recherche 5174, Centre National de la Recherche Scientifique-Université Paul Sabatier-Ecole Nationale de Formation Agronomique, 31062 Toulouse Cedex 9, France; eSchool of Natural Sciences, Trinity College Dublin, Dublin 2, Ireland; fTrinity Centre for Biodiversity Research, Trinity College Dublin, Dublin 2, Ireland; and gHerbarium, Library, Art and Archives, Royal Botanic Gardens, Kew, Surrey TW9 3AE, United Kingdom Edited by Elizabeth A. Kellogg, University of Missouri, St. Louis, MO, and accepted by the Editorial Board November 27, 2012 (received for review September 27, 2012) C4 photosynthesis is a series of anatomical and biochemical mod- metabolic modules that are suitable for the C4 pathway and can ifications to the typical C3 pathway that increases the productivity be recruited for this function through relatively few mutations of plants in warm, sunny, and dry conditions. Despite its complex- (6, 7). In addition, the photorespiratory pump based on glycine ity, it evolved more than 62 times independently in flowering decarboxylase is a likely evolutionary stable intermediate phe- plants. However, C4 origins are absent from most plant lineages notype on the road from C3 to C4 (3, 8). -
Plant Biodiversity Science, Discovery, and Conservation: Case Studies from Australasia and the Pacific
Plant Biodiversity Science, Discovery, and Conservation: Case Studies from Australasia and the Pacific Craig Costion School of Earth and Environmental Sciences Department of Ecology and Evolutionary Biology University of Adelaide Adelaide, SA 5005 Thesis by publication submitted for the degree of Doctor of Philosophy in Ecology and Evolutionary Biology July 2011 ABSTRACT This thesis advances plant biodiversity knowledge in three separate bioregions, Micronesia, the Queensland Wet Tropics, and South Australia. A systematic treatment of the endemic flora of Micronesia is presented for the first time thus advancing alpha taxonomy for the Micronesia-Polynesia biodiversity hotspot region. The recognized species boundaries are used in combination with all known botanical collections as a basis for assessing the degree of threat for the endemic plants of the Palau archipelago located at the western most edge of Micronesia’s Caroline Islands. A preliminary assessment is conducted utilizing the IUCN red list Criteria followed by a new proposed alternative methodology that enables a degree of threat to be established utilizing existing data. Historical records and archaeological evidence are reviewed to establish the minimum extent of deforestation on the islands of Palau since the arrival of humans. This enabled a quantification of population declines of the majority of plants endemic to the archipelago. In the state of South Australia, the importance of establishing concepts of endemism is emphasized even further. A thorough scientific assessment is presented on the state’s proposed biological corridor reserve network. The report highlights the exclusion from the reserve system of one of the state’s most important hotspots of plant endemism that is highly threatened from habitat fragmentation and promotes the use of biodiversity indices to guide conservation priorities in setting up reserve networks. -
Checklist of Microfungi on Grasses in Thailand (Excluding Bambusicolous Fungi)
Asian Journal of Mycology 1(1): 88–105 (2018) ISSN 2651-1339 www.asianjournalofmycology.org Article Doi 10.5943/ajom/1/1/7 Checklist of microfungi on grasses in Thailand (excluding bambusicolous fungi) Goonasekara ID1,2,3, Jayawardene RS1,2, Saichana N3, Hyde KD1,2,3,4 1 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 2 School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand 3 Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 4 World Agroforestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan, China Goonasekara ID, Jayawardene RS, Saichana N, Hyde KD 2018 – Checklist of microfungi on grasses in Thailand (excluding bambusicolous fungi). Asian Journal of Mycology 1(1), 88–105, Doi 10.5943/ajom/1/1/7 Abstract An updated checklist of microfungi, excluding bambusicolous fungi, recorded on grasses from Thailand is provided. The host plant(s) from which the fungi were recorded in Thailand is given. Those species for which molecular data is available is indicated. In total, 172 species and 35 unidentified taxa have been recorded. They belong to the main taxonomic groups Ascomycota: 98 species and 28 unidentified, in 15 orders, 37 families and 68 genera; Basidiomycota: 73 species and 7 unidentified, in 8 orders, 8 families and 18 genera; and Chytridiomycota: one identified species in Physodermatales, Physodermataceae. Key words – Ascomycota – Basidiomycota – Chytridiomycota – Poaceae – molecular data Introduction Grasses constitute the plant family Poaceae (formerly Gramineae), which includes over 10,000 species of herbaceous annuals, biennials or perennial flowering plants commonly known as true grains, pasture grasses, sugar cane and bamboo (Watson 1990, Kellogg 2001, Sharp & Simon 2002, Encyclopedia of Life 2018). -
The Evolutionary Ecology of C-4 Plants
This is a repository copy of The evolutionary ecology of C-4 plants. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/95833/ Version: Submitted Version Article: Christin, P-A. and Osborne, C.P. (2014) The evolutionary ecology of C-4 plants. New Phytologist, 204 (4). pp. 765-781. ISSN 0028-646X https://doi.org/10.1111/nph.13033 This is the pre-peer reviewed version of the following article: Christin, P.-A. and Osborne, C. P. (2014), The evolutionary ecology of C4 plants. New Phytologist, 204: 765–781, which has been published in final form at https://dx.doi.org/10.1111/nph.13033. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving (http://olabout.wiley.com/WileyCDA/Section/id-820227.html). Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request.