Checklist of Vascular Plants Recorded from Chatham Islands
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Volume 73, Number
New Zealand Science Review Vol 73 (3–4) 2016 Symposium on Systematics and Biodiversity in honour of Dr Dennis P. Gordon Official Journal of the New Zealand Association of Scientists ISSN 0028-8667 New Zealand Science Review Vol 73 (3–4) 2016 Official Journal of the New Zealand Association of Scientists P O Box 1874, Wellington www.scientists.org.nz A forum for the exchange of views on science and science policy Managing Editor: Allen Petrey Contents Guest Editor: Daniel Leduc Production Editor: Geoff Gregory Editorial .....................................................................................................................................................61 Proceedings of a Symposium on Systematics and Biodiversity: Past, Present and Future, National Institute of Water & Atmospheric Research, Wellington, April 2016 Bryozoa—not a minor phylum – Dennis P. Gordon and Mark J. Costello ..................................................63 The contribution of Dennis P. Gordon to the understanding of New Zealand Bryozoa – Abigail M Smith, Philip Bock and Peter Batson ................................................................................67 The study of taxonomy and systematics enhances ecological and conservation science – Ashley A. Rowden ............................................................................................................................72 Taxonomic research, collections and associated databases – and the changing science scene in New Zealand – Wendy Nelson .............................................................................79 -
Recent Changes in the Names of New Zealand Tree and Shrub Species
-- -- - Recent changes in the names of New Zealand tree and shrub species - Since the publication of 'Flora of New Zealand' Volume 1 (A- iii) Podocarpus dacydioides Dacrycarpus ducydioides lan 1961),covering indigenous ferns, conifers and dicots, there (iii)Podocarpus ferrugzneus Prumnopitys ferruginea have been major advances in taxonomic research and the clas- Podocarpus spicatus Prumnopitys taxijolia sification of many plant groups revised accordingly. Most of (iv1 Dacrydium cupressinum (unchanged) these changes have been summarised in the Nomina Nova (v)Dacrydium bidwillii Halocarpus bidwillii series published in the New Zealand Journal of Botany (Edgar Dacrydium bijorme Halocarpus bijormis 1971, Edgar and Connor 1978, 1983) and are included in re- Dacrydium kirkii Halocarpus kirkii cent books on New Zealand plants ie.g. Eagle 1982, Wilson (vi)Dacydium colensoi Lagarostrobos colensoi 1982). A number of these name changes affect important (vii)Dacrydium intermediurn Lepidothamnus intermedius forest plants and as several of these new names are now start- Dacrydium laxijolium Lepidotbamnus laxijolius ing to appear in the scientific literature, a list of changes af- (viii)Phyllocladus trichomanoidi~(unchanged) fecting tree and shrub taxa are given here. As a large number Phyllocladus glaucus (unchanged) of the readers of New Zealand Forestry are likely to use Poole Phyllocladus alpinus Phyllocladus aspleniijolius and Adams' "Trees and Shrubs of New Zealand" as their var. alpinus* * main reference for New Zealand forest plants, all the name changes are related to the fourth impression of this book. * It has been suggested that the Colenso name P, cunnin- it is important to realise that not all botanists necessarily ghamii (1884)should take precedence over the later (18891 ark agree with one particular name and you are not obliged to use name (P. -
Plant Charts for Native to the West Booklet
26 Pohutukawa • Oi exposed coastal ecosystem KEY ♥ Nurse plant ■ Main component ✤ rare ✖ toxic to toddlers coastal sites For restoration, in this habitat: ••• plant liberally •• plant generally • plant sparingly Recommended planting sites Back Boggy Escarp- Sharp Steep Valley Broad Gentle Alluvial Dunes Area ment Ridge Slope Bottom Ridge Slope Flat/Tce Medium trees Beilschmiedia tarairi taraire ✤ ■ •• Corynocarpus laevigatus karaka ✖■ •••• Kunzea ericoides kanuka ♥■ •• ••• ••• ••• ••• ••• ••• Metrosideros excelsa pohutukawa ♥■ ••••• • •• •• Small trees, large shrubs Coprosma lucida shining karamu ♥ ■ •• ••• ••• •• •• Coprosma macrocarpa coastal karamu ♥ ■ •• •• •• •••• Coprosma robusta karamu ♥ ■ •••••• Cordyline australis ti kouka, cabbage tree ♥ ■ • •• •• • •• •••• Dodonaea viscosa akeake ■ •••• Entelea arborescens whau ♥ ■ ••••• Geniostoma rupestre hangehange ♥■ •• • •• •• •• •• •• Leptospermum scoparium manuka ♥■ •• •• • ••• ••• ••• ••• ••• ••• Leucopogon fasciculatus mingimingi • •• ••• ••• • •• •• • Macropiper excelsum kawakawa ♥■ •••• •••• ••• Melicope ternata wharangi ■ •••••• Melicytus ramiflorus mahoe • ••• •• • •• ••• Myoporum laetum ngaio ✖ ■ •••••• Olearia furfuracea akepiro • ••• ••• •• •• Pittosporum crassifolium karo ■ •• •••• ••• Pittosporum ellipticum •• •• Pseudopanax lessonii houpara ■ ecosystem one •••••• Rhopalostylis sapida nikau ■ • •• • •• Sophora fulvida west coast kowhai ✖■ •• •• Shrubs and flax-like plants Coprosma crassifolia stiff-stemmed coprosma ♥■ •• ••••• Coprosma repens taupata ♥ ■ •• •••• •• -
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. -
Newsletter Number 29 September 1992 New Zealand Botanical Society Newsletter Number 29 September 1992
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 29 SEPTEMBER 1992 NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 29 SEPTEMBER 1992 CONTENTS News NZ Bot Soc News Call for nominations 2 New Zealand Threatened Indigenous Vascular Plant List .2 Regional Bot Soc News Auckland 5 Canterbury 6 Nelson 6 Rotorua 7 Waikato 7 Wellington 8 Obituary Margot Forde 8 Other News Distinguished New Zealand Scientist turns 100 9 Government Science structures reorganised 10 New Department consolidates Marine Science strengths 10 Notes and Reports Plant records Conservation status of titirangi (Hebe speciosa) 11 Senecio sterquilinus Ornduff in the Wellington Ecological District ....... 16 Trip reports Ecological Forum Excursion to South Patagonia and Tierra del Fuego (2) .... 17 Tangihua Fungal Foray, 20-24 May 1992 19 Biography/Bibliography Biographical Notes (6) Peter Goyen, an addition 20 Biographical Notes (7) Joshua Rutland 20 New Zealand Botanists and Fellowships of the Royal Society 22 Forthcoming Meetings/Conferences Lichen Techniques Workshop 22 Forthcoming Trips/Tours Seventh New Zealand Fungal Foray 22 Publications Checklist of New Zealand lichens 23 The mosses of New Zealand, special offer 24 Book review An illustrated guide to fungi on wood in New Zealand 25 Letters to the Editor New Zealand Botanical Society President: Dr Eric Godley Secretary/Treasurer: Anthony Wright Committee: Sarah Beadel, Ewen Cameron, Colin Webb, Carol West Address: New Zealand Botanical Society C/- Auckland Institute & Museum Private Bag 92018 AUCKLAND Subscriptions The 1992 ordinary and institutional subs are $14 (reduced to $10 if paid by the due date on the subscription invoice). The 1992 student sub, available to full-time students, is $7 (reduced to $5 if paid by the due date on the subscription invoice). -
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. -
INDEX for 2011 HERBALPEDIA Abelmoschus Moschatus—Ambrette Seed Abies Alba—Fir, Silver Abies Balsamea—Fir, Balsam Abies
INDEX FOR 2011 HERBALPEDIA Acer palmatum—Maple, Japanese Acer pensylvanicum- Moosewood Acer rubrum—Maple, Red Abelmoschus moschatus—Ambrette seed Acer saccharinum—Maple, Silver Abies alba—Fir, Silver Acer spicatum—Maple, Mountain Abies balsamea—Fir, Balsam Acer tataricum—Maple, Tatarian Abies cephalonica—Fir, Greek Achillea ageratum—Yarrow, Sweet Abies fraseri—Fir, Fraser Achillea coarctata—Yarrow, Yellow Abies magnifica—Fir, California Red Achillea millefolium--Yarrow Abies mariana – Spruce, Black Achillea erba-rotta moschata—Yarrow, Musk Abies religiosa—Fir, Sacred Achillea moschata—Yarrow, Musk Abies sachalinensis—Fir, Japanese Achillea ptarmica - Sneezewort Abies spectabilis—Fir, Himalayan Achyranthes aspera—Devil’s Horsewhip Abronia fragrans – Sand Verbena Achyranthes bidentata-- Huai Niu Xi Abronia latifolia –Sand Verbena, Yellow Achyrocline satureoides--Macela Abrus precatorius--Jequirity Acinos alpinus – Calamint, Mountain Abutilon indicum----Mallow, Indian Acinos arvensis – Basil Thyme Abutilon trisulcatum- Mallow, Anglestem Aconitum carmichaeli—Monkshood, Azure Indian Aconitum delphinifolium—Monkshood, Acacia aneura--Mulga Larkspur Leaf Acacia arabica—Acacia Bark Aconitum falconeri—Aconite, Indian Acacia armata –Kangaroo Thorn Aconitum heterophyllum—Indian Atees Acacia catechu—Black Catechu Aconitum napellus—Aconite Acacia caven –Roman Cassie Aconitum uncinatum - Monkshood Acacia cornigera--Cockspur Aconitum vulparia - Wolfsbane Acacia dealbata--Mimosa Acorus americanus--Calamus Acacia decurrens—Acacia Bark Acorus calamus--Calamus -
Cortaderia Selloana
Cortaderia selloana COMMON NAME Pampas grass FAMILY Poaceae AUTHORITY Cortaderia selloana (Schult. et Schult.f.) Asch. et Graebn. FLORA CATEGORY Vascular – Exotic STRUCTURAL CLASS Grasses NVS CODE CORSEL BRIEF DESCRIPTION Robust tussock with tall erect flowering stems bearing dense heads of white to pale pink flowers. HABITAT Terrestrial. A coastal and lowland plant found between sea level and 800 metres. Plant grows in sites of all levels of fertility from low to high. The plant grows in a wide variety of soils from pumice and coastal sands to Plimmerton. Jun 2006. Photographer: Jeremy heavy clay (Ford 1993). Coloniser of open ground (West, 1996). A plant Rolfe that occurs in low or disturbed forest (including plantations), wetlands, grasslands, scrub, cliffs, coastlines, islands, forest margins, riverbanks, shrubland, open areas, roadsides and sand dunes. The plant’s primary habitat is disturbed ground. FEATURES Large-clump-forming grass to 4 m+. Leaf base smooth or sparsely hairy, no white waxy surface (cf. toetoe - Austroderia - species). Leaves with conspicuous midrib which does not continue into leaf base, no secondary veins between midrib and leaf edge. Leaves bluish-green above, dark green below, snap across readily when folded and tugged (toetoe species have multiple ribs in the leaves, making the leaves difficult to snap across). Dead leaf bases spiral like wood shavings, which makes pampas grasses more flammable than toetoe species. Flower head erect, dense, fluffy, white-pinkish, fading to dirty white, (Jan)-Mar-Jun. SIMILAR TAXA Can be separated from native Austroderia (toetoe) by the prominent single midrib on the leaves (Austroderia species have several prominent veins.). -
ACT, Australian Capital 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. -
ABSTRACTS 117 Systematics Section, BSA / ASPT / IOPB
Systematics Section, BSA / ASPT / IOPB 466 HARDY, CHRISTOPHER R.1,2*, JERROLD I DAVIS1, breeding system. This effectively reproductively isolates the species. ROBERT B. FADEN3, AND DENNIS W. STEVENSON1,2 Previous studies have provided extensive genetic, phylogenetic and 1Bailey Hortorium, Cornell University, Ithaca, NY 14853; 2New York natural selection data which allow for a rare opportunity to now Botanical Garden, Bronx, NY 10458; 3Dept. of Botany, National study and interpret ontogenetic changes as sources of evolutionary Museum of Natural History, Smithsonian Institution, Washington, novelties in floral form. Three populations of M. cardinalis and four DC 20560 populations of M. lewisii (representing both described races) were studied from initiation of floral apex to anthesis using SEM and light Phylogenetics of Cochliostema, Geogenanthus, and microscopy. Allometric analyses were conducted on data derived an undescribed genus (Commelinaceae) using from floral organs. Sympatric populations of the species from morphology and DNA sequence data from 26S, 5S- Yosemite National Park were compared. Calyces of M. lewisii initi- NTS, rbcL, and trnL-F loci ate later than those of M. cardinalis relative to the inner whorls, and sepals are taller and more acute. Relative times of initiation of phylogenetic study was conducted on a group of three small petals, sepals and pistil are similar in both species. Petal shapes dif- genera of neotropical Commelinaceae that exhibit a variety fer between species throughout development. Corolla aperture of unusual floral morphologies and habits. Morphological A shape becomes dorso-ventrally narrow during development of M. characters and DNA sequence data from plastid (rbcL, trnL-F) and lewisii, and laterally narrow in M. -
Austroderia Richardii
Austroderia richardii COMMON NAME Toetoe SYNONYMS Arundo richardii Endl.; Arundo kakao Steud.; Arundo australis A.Rich.; Gynerium zeelandicum Steud.; Cortaderia richardii (Endl.) Zotov FAMILY Poaceae AUTHORITY Austroderia richardii (Endl.) N.P.Barker et H.P.Linder FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Kakanui Mountains, Otago. Photographer: John Yes Barkla ENDEMIC FAMILY No STRUCTURAL CLASS Grasses NVS CODE AUSRIC CHROMOSOME NUMBER 2n = 90 CURRENT CONSERVATION STATUS Cortaderia richardii. Photographer: John Smith- Dodsworth 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened DISTRIBUTION Endemic. Confined to the South Island. Possibly in the North Island, east of Cape Palliser. Naturalised in Tasmania. HABITAT Abundant, from the coast to subalpine areas. Common along stream banks, river beds, around lake margins, and in other wet places. Also found in sand dunes, especially along the Foveaux Strait. FEATURES Tall, gracile, slender tussock-forming grass up to 3 m tall when flowering. Leaf sheath glabrous, green, covered in white wax. Ligule 3.5 mm. Collar brown, basally glabrous, upper surface with short, stiff hairs surmounting ribs. Leaf blade 2-3 x 0.25 m, green, dark-green, often somewhat glaucous, upper side with thick weft of hairs at base, otherwise sparsely hairy up midrib with abundant, minute prickle teeth throughout. Undersurface with leaf with 5 mm long hairs near leaf margins, otherwise harshly scabrid. Culm up to 3 m, inflorescence portion up to 1 m tall, pennant-shaped, drooping, narrowly plumose. Spikelets numerous, 25 mm with 3 florets per spikelet. Glumes equal, > or equal to florets, 1- or 3-nerved. Lemma 10 mm, scabrid.