MVG 21 – Other Grasslands, Herblands, Sedgelands and Rushlands
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The Angiosperm Flora of Singapore Part 2 PHILYDRACEAE
The Angiosperm Flora of Singapore Part 2 PHILYDRACEAE R.M.K. SAUNDERS Department of Ecology & Biodiversity, The Univenity of Hong Kong Pokfulam Road . Hong Kong Philydrum Banks & Sol. ex Gaertn Fruct. sem. pl. 1 (1788) 62, t. 16: Ridl.. F1. Malay Penins. 4 (1924) 347; Skott5b.. Bull. Jard. bot. Etat Brux. scr. 3. 13: (1933) 11 I; Skottsb., FI. Malcs. scr. 1, 4:1(1048) 5. Erect, perennial, caespitose herbs with a short rhizome. Lenves densely rosulate, equitant. 2-ranked; linear, fleshy, parallel-veined, sheathing at base. Inflorescence a simple or paniculate terminal spike; scape 1 m or longer, with few cauline leaves gradually replaced by alternate bracts. Flowers bisexual; zygomorphic; sessile, solitary in axil of spathaceous bracts; bracts enclosing flower buds, reflexed at anthesis, later embracing the fruit; perianth corolline, 4-segmented, 2-seriate, persistent as fruit cover, yellow, 2 outer tepals larger, adaxial and abaxial respectively, 2 inner tepals smaller, lateral: stamen single, filament flattened, adnate with base of inner and adaxial tepals, anther dorsifixed, 2-loculate, spirally twisted, extrorse, opening lengthwise by slits, pollen grains in tetrads, staminodes cuneate, acute, shorter than fertile stamen: ovary single, superior, 3-loculate, with parietal placentation, ovules many per locule, anatropous; style simple. Fruit a persistent triangular-oblong loculicidal capsule with 3 valves. Seeds with corona and spirally-striate testa, many per locule; embryo straight. Distribution - Monotypic genus, occurring in South Japan, Taiwan, South-East China, Indo-China, Malay Peninsula, Guam, South New Guinea and North, East and South-East Australia (Hamann, 1966a). P. lnni~ginosum is reported to be extinct in Singapore (Keng, 1987) but was previously collected in Bedok. -
Edition 2 from Forest to Fjaeldmark the Vegetation Communities Highland Treeless Vegetation
Edition 2 From Forest to Fjaeldmark The Vegetation Communities Highland treeless vegetation Richea scoparia Edition 2 From Forest to Fjaeldmark 1 Highland treeless vegetation Community (Code) Page Alpine coniferous heathland (HCH) 4 Cushion moorland (HCM) 6 Eastern alpine heathland (HHE) 8 Eastern alpine sedgeland (HSE) 10 Eastern alpine vegetation (undifferentiated) (HUE) 12 Western alpine heathland (HHW) 13 Western alpine sedgeland/herbland (HSW) 15 General description Rainforest and related scrub, Dry eucalypt forest and woodland, Scrub, heathland and coastal complexes. Highland treeless vegetation communities occur Likewise, some non-forest communities with wide within the alpine zone where the growth of trees is environmental amplitudes, such as wetlands, may be impeded by climatic factors. The altitude above found in alpine areas. which trees cannot survive varies between approximately 700 m in the south-west to over The boundaries between alpine vegetation communities are usually well defined, but 1 400 m in the north-east highlands; its exact location depends on a number of factors. In many communities may occur in a tight mosaic. In these parts of Tasmania the boundary is not well defined. situations, mapping community boundaries at Sometimes tree lines are inverted due to exposure 1:25 000 may not be feasible. This is particularly the or frost hollows. problem in the eastern highlands; the class Eastern alpine vegetation (undifferentiated) (HUE) is used in There are seven specific highland heathland, those areas where remote sensing does not provide sedgeland and moorland mapping communities, sufficient resolution. including one undifferentiated class. Other highland treeless vegetation such as grasslands, herbfields, A minor revision in 2017 added information on the grassy sedgelands and wetlands are described in occurrence of peatland pool complexes, and other sections. -
Introduction Methods Results
Papers and Proceedings Royal Society ofTasmania, Volume 1999 103 THE CHARACTERISTICS AND MANAGEMENT PROBLEMS OF THE VEGETATION AND FLORA OF THE HUNTINGFIELD AREA, SOUTHERN TASMANIA by J.B. Kirkpatrick (with two tables, four text-figures and one appendix) KIRKPATRICK, J.B., 1999 (31:x): The characteristics and management problems of the vegetation and flora of the Huntingfield area, southern Tasmania. Pap. Proc. R. Soc. Tasm. 133(1): 103-113. ISSN 0080-4703. School of Geography and Environmental Studies, University ofTasmania, GPO Box 252-78, Hobart, Tasmania, Australia 7001. The Huntingfield area has a varied vegetation, including substantial areas ofEucalyptus amygdalina heathy woodland, heath, buttongrass moorland and E. amygdalina shrubbyforest, with smaller areas ofwetland, grassland and E. ovata shrubbyforest. Six floristic communities are described for the area. Two hundred and one native vascular plant taxa, 26 moss species and ten liverworts are known from the area, which is particularly rich in orchids, two ofwhich are rare in Tasmania. Four other plant species are known to be rare and/or unreserved inTasmania. Sixty-four exotic plantspecies have been observed in the area, most ofwhich do not threaten the native biodiversity. However, a group offire-adapted shrubs are potentially serious invaders. Management problems in the area include the maintenance ofopen areas, weed invasion, pathogen invasion, introduced animals, fire, mechanised recreation, drainage from houses and roads, rubbish dumping and the gathering offirewood, sand and plants. Key Words: flora, forest, heath, Huntingfield, management, Tasmania, vegetation, wetland, woodland. INTRODUCTION species with the most cover in the shrub stratum (dominant species) was noted. If another species had more than half The Huntingfield Estate, approximately 400 ha of forest, the cover ofthe dominant one it was noted as a codominant. -
Luronium Natans
Luronium natans Status UK Biodiversity Action Plan Priority species. Nationally Scarce. Schedule 8, Wildlife & Countryside Act (1981). IUCN Threat category: Least concern (2005). Taxonomy Magnoliopsida: Alismataceae Scientific names: Luronium natans (L.) Raf. Common names: Floating Water-plantain, Dŵr-lyriad Nofiadwy Luronium natans (Alisma natans L.) is a distinct member of the Water-plantain family, and is the only representative of its genus. Biology & Distribution Luronium is under-recorded due to its generally submerged aquatic habitat, shy flowering, great phenotypic plasticity and similarity to other aquatic plants. The leaves do not tend to be caught on NB. Floating grapnels or get washed ashore and often the easiest leaves are way to find it in water is to dive or use a long hooked usually more blunt than pole. It may also be found easily when exposed in Submerged illustrated seasonal ponds. The species can grow in both isolated leaves clumps or extensive lawns on the bottom of canals, lochs, ponds, etc., in water up to 4 m depth. Figure 1. Luronium natans (from J. Sowerby & J. E. Sowerby Although its stronghold is Wales and the Welsh (1902). English Botany. London) borders, it has been found recently in Cumbria, Scotland and Ireland where it is probably an over- that they have flat leaves). In still or gently flowing looked native rather than a recent arrival; it may well water the submerged rosette leaves are typically c. 5-15 be more widespread still. cm long, strongly flattened, linear-triangular, tapering uniformly from a base c. 4-7 mm wide to a fine acute Identification & Field survey tip. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck 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. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Vicariance, Climate Change, Anatomy and Phylogeny of Restionaceae
Botanical Journal of the Linnean Society (2000), 134: 159–177. With 12 figures doi:10.1006/bojl.2000.0368, available online at http://www.idealibrary.com on Under the microscope: plant anatomy and systematics. Edited by P. J. Rudall and P. Gasson Vicariance, climate change, anatomy and phylogeny of Restionaceae H. P. LINDER FLS Bolus Herbarium, University of Cape Town, Rondebosch 7701, South Africa Cutler suggested almost 30 years ago that there was convergent evolution between African and Australian Restionaceae in the distinctive culm anatomical features of Restionaceae. This was based on his interpretation of the homologies of the anatomical features, and these are here tested against a ‘supertree’ phylogeny, based on three separate phylogenies. The first is based on morphology and includes all genera; the other two are based on molecular sequences from the chloroplast genome; one covers the African genera, and the other the Australian genera. This analysis corroborates Cutler’s interpretation of convergent evolution between African and Australian Restionaceae. However, it indicates that for the Australian genera, the evolutionary pathway of the culm anatomy is much more complex than originally thought. In the most likely scenario, the ancestral Restionaceae have protective cells derived from the chlorenchyma. These persist in African Restionaceae, but are soon lost in Australian Restionaceae. Pillar cells and sclerenchyma ribs evolve early in the diversification of Australian Restionaceae, but are secondarily lost numerous times. In some of the reduction cases, the result is a very simple culm anatomy, which Cutler had interpreted as a primitively simple culm type, while in other cases it appears as if the functions of the ribs and pillars may have been taken over by a new structure, protective cells developed from epidermal, rather than chlorenchyma, cells. -
Alisma Lanceolatum
Alisma lanceolatum COMMON NAME Water plantain FAMILY Alismataceae AUTHORITY Alisma lanceolatum With. FLORA CATEGORY Vascular – Exotic STRUCTURAL CLASS Herbs - Monocots NVS CODE ALILAN BRIEF DESCRIPTION A marginal aquatic plant, with lance-shaped leaves, with many tiny pink flowers held on a pyramid-shaped inflorescence, much taller than the rest of the plant. DISTRIBUTION Scattered in Hawkes Bay, Wellington and Canterbury. HABITAT Margins of still and slow flowing water bodies and wetlands. FEATURES Upper Hutt. Dec 2006. Photographer: Jeremy Leafy emergent perennial herb up to c. 1 m high, although non-flowering Rolfe plants are much shorter. Aerial parts die off over winter to the rootstock. Leaves all basal, broad ovate 7-23 (28) × 2-5 cm, with a tapered base with a long petiole up to or exceeding the leaf blade. Petiole is semi- circular in cross-section (D-shaped). Submerged or floating leaved plants sometimes occur, these have narrower than emergent leaves. Inflorescence a large, much-branched panicle; branches whorled. Flowers usually pale lilac, c. 1 cm across. C. 20 rounded and flattened seeds (achenes) c. 2.5 mm long, in a dense circular head. SIMILAR TAXA Alisma plantago-aquatica has broader lance-shaped leaves and lilac rather than pink coloured flowers. Sagittaria platyphylla has larger flowers on a smaller inflorescence and triangular petioles. FLOWERING Summer FLOWER COLOURS Red/Pink FRUITING Summer to autumn Upper Hutt. Dec 2006. Photographer: Jeremy Rolfe LIFE CYCLE Spreads by waterfowl and water dispersed seed. YEAR NATURALISED 1895 ORIGIN Native to Europe, North Africa and West Asia. REASON FOR INTRODUCTION Possibly ornamental pond plant, or a seed or soil contaminant. -
'A New Subfamilial and Tribal Classification of Restionaceae
Briggs, B G; Linder, H P (2009). A new subfamilial and tribal classification of Restionaceae (Poales). Telopea, 12(3):333-345. Postprint available at: http://www.zora.uzh.ch University of Zurich Posted at the Zurich Open Repository and Archive, University of Zurich. Zurich Open Repository and Archive http://www.zora.uzh.ch Originally published at: Telopea 2009, 12(3):333-345. Winterthurerstr. 190 CH-8057 Zurich http://www.zora.uzh.ch Year: 2009 A new subfamilial and tribal classification of Restionaceae (Poales) Briggs, B G; Linder, H P Briggs, B G; Linder, H P (2009). A new subfamilial and tribal classification of Restionaceae (Poales). Telopea, 12(3):333-345. Postprint available at: http://www.zora.uzh.ch Posted at the Zurich Open Repository and Archive, University of Zurich. http://www.zora.uzh.ch Originally published at: Telopea 2009, 12(3):333-345. Telopea 12(3) 333–345 A new subfamilial and tribal classification of Restionaceae (Poales) Barbara G. Briggs1 and H. Peter Linder2 1Botanic Gardens Trust Sydney, Mrs Macquaries Road, Sydney NSW 2000, Australia. Email: [email protected] 2Institute of Systematic Botany, University of Zurich, Zollikerrstrasse 107, CH-8008 Zurich, Switzerland Email: [email protected] Abstract Restionoideae Link, with the newly described Sporadanthoideae and Leptocarpoideae, represent major clades of Restionaceae distinguished by analyses of chloroplast DNA data. These subfamilies are supported by features of morphology, culm anatomy, pollen and phytochemistry. Sporadanthoideae occur in Australia and New Zealand, Leptocarpoideae principally in Australia but with representatives also in New Zealand, New Guinea, Aru Islands, Malesia, Hainan Island and Chile, while Restionoideae are in sub-Saharan Africa and Madagascar. -
List of Plant Species List of Plant Species
List of plant species List of Plant Species Contents Amendment history .......................................................................................................................... 2 1 Introduction ...................................................................................................................................... 3 1.1 Application ........................................................................................................................... 3 1.2 Relationship with planning scheme ..................................................................................... 3 1.3 Purpose ............................................................................................................................... 3 1.4 Aim ...................................................................................................................................... 3 1.5 Who should use this manual? ............................................................................................. 3 2 Special consideration ....................................................................................................................... 3 3 Variations ......................................................................................................................................... 4 4 Relationship ..................................................................................................................................... 4 Appendix A – Explanatory notes & definitions ....................................................................................... -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
The 1770 Landscape of Botany Bay, the Plants Collected by Banks and Solander and Rehabilitation of Natural Vegetation at Kurnell
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Hochschulschriftenserver - Universität Frankfurt am Main Backdrop to encounter: the 1770 landscape of Botany Bay, the plants collected by Banks and Solander and rehabilitation of natural vegetation at Kurnell Doug Benson1 and Georgina Eldershaw2 1Botanic Gardens Trust, Mrs Macquaries Rd Sydney 2000 AUSTRALIA email [email protected] 2Parks & Wildlife Division, Dept of Environment and Conservation (NSW), PO Box 375 Kurnell NSW 2231 AUSTRALIA email [email protected] Abstract: The first scientific observations on the flora of eastern Australia were made at Botany Bay in April–May 1770. We discuss the landscapes of Botany Bay and particularly of the historic landing place at Kurnell (lat 34˚ 00’ S, long 151˚ 13’ E) (about 16 km south of central Sydney), as described in the journals of Lieutenant James Cook and Joseph Banks on the Endeavour voyage in 1770. We list 132 plant species that were collected at Botany Bay by Banks and Daniel Solander, the first scientific collections of Australian flora. The list is based on a critical assessment of unpublished lists compiled by authors who had access to the collection of the British Museum (now Natural History Museum), together with species from material at National Herbarium of New South Wales that has not been previously available. The list includes Bidens pilosa which has been previously regarded as an introduced species. In 1770 the Europeans set foot on Aboriginal land of the Dharawal people. Since that time the landscape has been altered in response to a succession of different land-uses; farming and grazing, commemorative tree planting, parkland planting, and pleasure ground and tourist visitation. -
Flora of New Zealand Seed Plants
FLORA OF NEW ZEALAND SEED PLANTS ALISMATACEAE K.A. FORD & P.D. CHAMPION Fascicle 7 – DECEMBER 2020 © Landcare Research New Zealand Limited 2020. Unless indicated otherwise for specific items, this copyright work is licensed under the Creative Commons Attribution 4.0 International licence Attribution if redistributing to the public without adaptation: "Source: Manaaki Whenua – Landcare Research" Attribution if making an adaptation or derivative work: "Sourced from Manaaki Whenua – Landcare Research" See Image Information for copyright and licence details for images. CATALOGUING IN PUBLICATION Ford, Kerry A. (Kerry Alison) Flora of New Zealand : seed plants. Fascicle 7, Alismataceae / K.A. Ford and P.D. Champion. -- Lincoln, N.Z. : Manaaki Whenua Press, 2020. 1 online resource ISBN 978-0- 947525-67-5 (pdf) ISBN 978-0-478-34762-3 (set) 1.Alismataceae -- New Zealand – Identification. I. Champion, P.D. II. Title. III. Manaaki Whenua – Landcare Research New Zealand Ltd. UDC 582.536 (931) DC 584.720993 DOI: 10.7931/jwc3-zg41 This work should be cited as: Ford K.A. & Champion P.D. 2020: Alismataceae. In: Wilton, A.D. (ed.) Flora of New Zealand — Seed Plants. Fascicle 7. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/jwc3-zg41 Date submitted: 12 Jun 2019; Date accepted: 4 Jun 2020; Date published: 2 January 2021 Cover image: Alisma lanceolatum. Flower showing acute petal apices. Contents Introduction..............................................................................................................................................1