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Evaluation of a Proposed Significant Natural Area at Mt Iron, Wanaka
EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA R3762 EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA Coprosma shrubland on the southwest faces at the Allenby Farms site, Mt Iron. Contract Report No. 3762 March 2017 (Revised and updated) Project Team: Kelvin Lloyd - Report author: vegetation and flora Mandy Tocher - Report author: herpetofauna Brian Patrick - Report author: invertebrates Prepared for: Allenby Farms Ltd P.O. Box 196 Wanaka 9343 DUNEDIN OFFICE: 764 CUMBERLAND STREET, DUNEDIN 9016 Ph 03-477-2096, 03-477-2095 HEAD OFFICE: 99 SALA STREET, P.O. BOX 7137, TE NGAE, ROTORUA Ph 07-343-9017, 07-343-9018; email [email protected], www.wildlands.co.nz CONTENTS 1. INTRODUCTION 1 2. SITE CONTEXT 1 3. METHODS 1 4. ECOLOGICAL CONTEXT 4 5. INDIGENOUS VEGETATION AND HABITATS 5 5.1 Kānuka scrub and shrubland 5 5.2 Coprosma scrub and shrubland 6 5.3 Exotic grassland and herbfield 7 5.4 Swale turf 8 5.5 Cushionfield 8 6. FLORA 8 6.1 Species richness 8 6.2 Threatened and At Risk plant species 12 6.3 Pest plants 12 7. BIRDS 13 8. LIZARDS 14 8.1 Overview 14 8.2 “Remove from SNA” zone 14 8.3 Alternate SNA 18 9. INVERTEBRATES 18 9.1 Overview 18 9.2 Mixed Coprosma-dominant shrubland 18 9.3 Kānuka scrub and shrubland 19 9.4 Rock outcrop habitats 19 9.5 Open grassland and turf 19 10. PEST ANIMALS 20 11. ECOLOGICAL VALUES 20 11.1 District Plan (2009) - Section 6c Significance 20 11.2 Proposed District Plan - Section 6c Significance from Policy 33.2.1.9 22 11.3 Significance summary 23 12. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Rare Or Threatened Vascular Plant Species of Wollemi National Park, Central Eastern New South Wales
Rare or threatened vascular plant species of Wollemi National Park, central eastern New South Wales. Stephen A.J. Bell Eastcoast Flora Survey PO Box 216 Kotara Fair, NSW 2289, AUSTRALIA Abstract: Wollemi National Park (c. 32o 20’– 33o 30’S, 150o– 151oE), approximately 100 km north-west of Sydney, conserves over 500 000 ha of the Triassic sandstone environments of the Central Coast and Tablelands of New South Wales, and occupies approximately 25% of the Sydney Basin biogeographical region. 94 taxa of conservation signiicance have been recorded and Wollemi is recognised as an important reservoir of rare and uncommon plant taxa, conserving more than 20% of all listed threatened species for the Central Coast, Central Tablelands and Central Western Slopes botanical divisions. For a land area occupying only 0.05% of these divisions, Wollemi is of paramount importance in regional conservation. Surveys within Wollemi National Park over the last decade have recorded several new populations of signiicant vascular plant species, including some sizeable range extensions. This paper summarises the current status of all rare or threatened taxa, describes habitat and associated species for many of these and proposes IUCN (2001) codes for all, as well as suggesting revisions to current conservation risk codes for some species. For Wollemi National Park 37 species are currently listed as Endangered (15 species) or Vulnerable (22 species) under the New South Wales Threatened Species Conservation Act 1995. An additional 50 species are currently listed as nationally rare under the Briggs and Leigh (1996) classiication, or have been suggested as such by various workers. Seven species are awaiting further taxonomic investigation, including Eucalyptus sp. -
Rock Garden Quarterly
ROCK GARDEN QUARTERLY VOLUME 53 NUMBER 1 WINTER 1995 COVER: Aquilegia scopulorum with vespid wasp by Cindy Nelson-Nold of Lakewood, Colorado All Material Copyright © 1995 North American Rock Garden Society ROCK GARDEN QUARTERLY BULLETIN OF THE NORTH AMERICAN ROCK GARDEN SOCIETY formerly Bulletin of the American Rock Garden Society VOLUME 53 NUMBER 1 WINTER 1995 FEATURES Alpine Gesneriads of Europe, by Darrell Trout 3 Cassiopes and Phyllodoces, by Arthur Dome 17 Plants of Mt. Hutt, a New Zealand Preview, by Ethel Doyle 29 South Africa: Part II, by Panayoti Kelaidis 33 South African Sampler: A Dozen Gems for the Rock Garden, by Panayoti Kelaidis 54 The Vole Story, by Helen Sykes 59 DEPARTMENTS Plant Portrait 62 Books 65 Ramonda nathaliae 2 ROCK GARDEN QUARTERLY VOL. 53:1 ALPINE GESNERIADS OF EUROPE by Darrell Trout J. he Gesneriaceae, or gesneriad Institution and others brings the total family, is a diverse family of mostly Gesneriaceae of China to a count of 56 tropical and subtropical plants with genera and about 413 species. These distribution throughout the world, should provide new horticultural including the north and south temper• material for the rock garden and ate and tropical zones. The 125 genera, alpine house. Yet the choicest plants 2850-plus species include terrestrial for the rock garden or alpine house and epiphytic herbs, shrubs, vines remain the European genera Ramonda, and, rarely, small trees. Botanically, Jancaea, and Haberlea. and in appearance, it is not always easy to separate the family History Gesneriaceae from the closely related The family was named for Konrad Scrophulariaceae (Verbascum, Digitalis, von Gesner, a sixteenth century natu• Calceolaria), the Orobanchaceae, and ralist. -
Patterns in Ericaceae: New Phylogenetic Analyses
BS 55 479 Origins and biogeographic patterns in Ericaceae: New insights from recent phylogenetic analyses Kathleen A. Kron and James L. Luteyn Kron, KA. & Luteyn, J.L. 2005. Origins and biogeographic patterns in Ericaceae: New insights from recent phylogenetic analyses. Biol. Skr. 55: 479-500. ISSN 0366-3612. ISBN 87-7304-304-4. Ericaceae are a diverse group of woody plants that span the temperate and tropical regions of the world. Previous workers have suggested that Ericaceae originated in Gondwana, but recent phy logenetic studies do not support this idea. The theory of a Gondwanan origin for the group was based on the concentration of species richness in the Andes, southern Africa, and the southwest Pacific islands (most of which are thought to be of Gondwanan origin). The Andean diversity is comprised primarily of Vaccinieae with more than 800 species occurring in northern South America, Central America, and the Antilles. In the Cape Region of South Africa the genus Erica is highly diverse with over 600 species currently recognized. In the southwest Pacific islands, Vac cinieae and Rhodoreae are very diverse with over 290 species of Rhododendron (sect. Vireya) and approximately 500 species of Vaccinieae (I)imorphanthera, Paphia, Vaccinium). Recent phyloge netic studies have also shown that the Styphelioideae (formerly Epacridaceae) are included within Ericaceae, thus adding a fourth extremely diverse group (approximately 520 species) in areas considered Gondwanan in origin. Phylogenetic studies of the family on a global scale, how ever, have indicated that these highly diverse “Gondwanan” groups are actually derived from within Ericaceae. Both Fitch parsimony character optimization (using MacClade 4.0) and disper- sal-vicariance analysis (DIVA) indicate that Ericaceae is Laurasian in origin. -
Post-Fire Recovery of Woody Plants in the New England Tableland Bioregion
Post-fire recovery of woody plants in the New England Tableland Bioregion Peter J. ClarkeA, Kirsten J. E. Knox, Monica L. Campbell and Lachlan M. Copeland Botany, School of Environmental and Rural Sciences, University of New England, Armidale, NSW 2351, AUSTRALIA. ACorresponding author; email: [email protected] Abstract: The resprouting response of plant species to fire is a key life history trait that has profound effects on post-fire population dynamics and community composition. This study documents the post-fire response (resprouting and maturation times) of woody species in six contrasting formations in the New England Tableland Bioregion of eastern Australia. Rainforest had the highest proportion of resprouting woody taxa and rocky outcrops had the lowest. Surprisingly, no significant difference in the median maturation length was found among habitats, but the communities varied in the range of maturation times. Within these communities, seedlings of species killed by fire, mature faster than seedlings of species that resprout. The slowest maturing species were those that have canopy held seed banks and were killed by fire, and these were used as indicator species to examine fire immaturity risk. Finally, we examine whether current fire management immaturity thresholds appear to be appropriate for these communities and find they need to be amended. Cunninghamia (2009) 11(2): 221–239 Introduction Maturation times of new recruits for those plants killed by fire is also a critical biological variable in the context of fire Fire is a pervasive ecological factor that influences the regimes because this time sets the lower limit for fire intervals evolution, distribution and abundance of woody plants that can cause local population decline or extirpation (Keith (Whelan 1995; Bond & van Wilgen 1996; Bradstock et al. -
E29695d2fc942b3642b5dc68ca
ISSN 1409-3871 VOL. 9, No. 1—2 AUGUST 2009 Orchids and orchidology in Central America: 500 years of history CARLOS OSSENBACH INTERNATIONAL JOURNAL ON ORCHIDOLOGY LANKESTERIANA INTERNATIONAL JOURNAL ON ORCHIDOLOGY Copyright © 2009 Lankester Botanical Garden, University of Costa Rica Effective publication date: August 30, 2009 Layout: Jardín Botánico Lankester. Cover: Chichiltic tepetlauxochitl (Laelia speciosa), from Francisco Hernández, Rerum Medicarum Novae Hispaniae Thesaurus, Rome, Jacobus Mascardus, 1628. Printer: Litografía Ediciones Sanabria S.A. Printed copies: 500 Printed in Costa Rica / Impreso en Costa Rica R Lankesteriana / International Journal on Orchidology No. 1 (2001)-- . -- San José, Costa Rica: Editorial Universidad de Costa Rica, 2001-- v. ISSN-1409-3871 1. Botánica - Publicaciones periódicas, 2. Publicaciones periódicas costarricenses LANKESTERIANA i TABLE OF CONTENTS Introduction 1 Geographical and historical scope of this study 1 Political history of Central America 3 Central America: biodiversity and phytogeography 7 Orchids in the prehispanic period 10 The area of influence of the Chibcha culture 10 The northern region of Central America before the Spanish conquest 11 Orchids in the cultures of Mayas and Aztecs 15 The history of Vanilla 16 From the Codex Badianus to Carl von Linné 26 The Codex Badianus 26 The expedition of Francisco Hernández to New Spain (1570-1577) 26 A new dark age 28 The “English American” — the journey through Mexico and Central America of Thomas Gage (1625-1637) 31 The renaissance of science -
Interactive Effects of Climate Change and Species Composition on Alpine Biodiversity and Ecosystem Dynamics
Interactive effects of climate change and plant invasion on alpine biodiversity and ecosystem dynamics Justyna Giejsztowt M.Sc., 2013 University of Poitiers, France; Christian-Albrechts University, Germany B. Sc., 2010 University of Canterbury, New Zealand A thesis submitted to Victoria University of Wellington in partial fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological Sciences Victoria University of Wellington Te Herenga Waka 2019 i ii This thesis was conducted under the supervision of Dr Julie R. Deslippe (primary supervisor) Victoria University of Wellington Wellington, New Zealand And Dr Aimée T. Classen (secondary supervisor) University of Vermont Burlington, United States of America iii iv “May your mountains rise into and above the clouds.” -Edward Abbey v vi Abstract Drivers of global change have direct impacts on the structure of communities and functioning of ecosystems, and interactions between drivers may buffer or exacerbate these direct effects. Interactions among drivers can lead to complex non-linear outcomes for ecosystems, communities and species, but are infrequently quantified. Through a combination of experimental, observational and modelling approaches, I address critical gaps in our understanding of the interactive effects of climate change and plant invasion, using Tongariro National Park (TNP; New Zealand) as a model. TNP is an alpine ecosystem of cultural significance which hosts a unique flora with high rates of endemism. TNP is invaded by the perennial shrub Calluna vulgaris (L.) Hull. My objectives were to: 1) determine whether species- specific phenological shifts have the potential to alter the reproductive capacity of native plants in landscapes affected by invasion; 2) determine whether the effect of invasion intensity on the Species Area Relationship (SAR) of native alpine plant species is influenced by environmental stress; 3) develop a novel modelling framework that would account for density-dependent competitive interactions between native species and C. -
Astereae, Asteraceae) Downloaded from by Guest on 04 September 2019 GISELA SANCHO1*, PETER J
bs_bs_banner Botanical Journal of the Linnean Society, 2015, 177, 78–95. With 5 figures Late Cenozoic diversification of the austral genus Lagenophora (Astereae, Asteraceae) Downloaded from https://academic.oup.com/botlinnean/article-abstract/177/1/78/2416348 by guest on 04 September 2019 GISELA SANCHO1*, PETER J. DE LANGE FLS2, MARIANO DONATO3, JOHN BARKLA4 and STEVE J. WAGSTAFF5 1División Plantas Vasculares, Museo de La Plata, FCNYM, UNLP, Paseo del Bosque s.n., La Plata, 1900, Buenos Aires, Argentina 2Ecosystems and Species Unit, Department of Conservation, Private Bag 68908, Newton 1145, Auckland, New Zealand 3ILPLA, Instituto de Limnología Dr. Raúl A. Ringuelet, FCNYM, UNLP and CONICET, 122 and 60, La Plata, 1900, Buenos Aires, Argentina 4Otago Conservancy, Department of Conservation, PO Box 5244, Dunedin 9058, New Zealand 5Allan Herbarium, Landcare Research, PO Box 69040, Lincoln 7640, New Zealand Received 14 March 2014; revised 23 May 2014; accepted for publication 30 August 2014 Lagenophora (Astereae, Asteraceae) has 14 species in New Zealand, Australia, Asia, southern South America, Gough Island and Tristan da Cunha. Phylogenetic relationships in Lagenophora were inferred using nuclear and plastid DNA regions. Reconstruction of spatio-temporal evolution was estimated using parsimony, Bayesian inference and likelihood methods, a Bayesian relaxed molecular clock and ancestral area and habitat reconstruc- tions. Our results support a narrow taxonomic concept of Lagenophora including only a core group of species with one clade diversifying in New Zealand and another in South America. The split between the New Zealand and South American Lagenophora dates from 11.2 Mya [6.1–17.4 95% highest posterior density (HPD)]. -
Olearia Adenocarpa PO Box 743 Invercargill Small–Leaved Tree Daisy May 2007
Published by Department of Conservation Southland Conservancy Olearia adenocarpa PO Box 743 Invercargill SMALL–LEAVED TREE DAISY May 2007 Olearia adenocarpa is one of eight rare Olearia species included in the Small-leaved Tree Daisy National Recovery Plan. A separate fact sheet is available for each species. The aim of the factsheets is to en- courage public awareness of these distinctive New Zealand species and to find compatible ways of managing the places where they exist. A first step towards this is to help people recognise the plants and take an interest in their welfare. Description Olearia adenocarpa is a newly recog- generally occur as scattered individuals nised species described and named in and are not abundant at any one site 2004. It had previously been mis-identi- because its former communities and fied as Olearia odorata or Olearia vir- habitats are generally degraded to un- gata. It is a deciduous shrub up to 1.2 improved dry grassland. Only one site m high, the main branches of which are is fenced and managed for conservation short-lived (<12 years). It regularly pro- purposes. duces new branches from at and below ground level and has opposite leaves in clusters. Leaves are egg shaped 3–14mm long × 2–4 mm wide, and are hairy on the underside. Flowers appear in clusters in January and February. The dry seeds are covered with hairs which distinguish it from other species. Habitat Olearia adeno - carpa occurs on the dry stony ter- races and channels bordering braided riverbeds where its most common asso- ciate appears to be matagouri (Discaria Sketches not to scale toumatou). -
Celmisia Spectabilis Subsp. Magnifica
Celmisia spectabilis subsp. magnifica COMMON NAME Cotton daisy, mountain daisy, shephards tobacco SYNONYMS Celmisia spectabilis var. magnifica Allan FAMILY Asteraceae AUTHORITY Celmisia spectabilis subsp. magnifica (Allan) Given FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Mount Somers. Feb 1982. Photographer: Colin Ogle No ENDEMIC FAMILY No STRUCTURAL CLASS Herbs - Dicotyledonous composites NVS CODE CELSSM CHROMOSOME NUMBER 2n = c.108 Mount Somers. Feb 1982. Photographer: Colin CURRENT CONSERVATION STATUS Ogle 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened DISTRIBUTION Endemic. South Island: Big Ben Range and Acheron Valley just north of Rakaia River, south to the Hunters Hills and Mount Studholme. HABITAT Alpine and subalpine grassland and herbfield rocky sites FEATURES Woody-based herb forming mats or cushions 2.0 m diameter; with branchlets arising from a usually hidden simple or multicipital stock. Living leaves in rosettes at the tips of branchlets, the whole forming a cushion or mat. Leaf sheaths densely imbricate and compacted, forming a pseudostem. Leaf lamina 70-290 × 1-45 mm, (ratio of length to width 5.6-10); coriaceous, usually lanceolate-oblong to narrowly ovate; upper surface shining and sulcate: lower surface densely covered in soft felted pale buff tomentum, midrib distinct; tip acute; margins entire and recurved, occasionally minutely toothed, with the lamina base cuneate to cuneate-truncate; sheath green to purple. Petiole thin with evident veins. Scape densely clad in floccose white hairs, stout, up to 300 mm long, bracteate, monocephalous Corolla of disc florets and achenes often with uniseriate and biseriate hairs, mostly hairy, rarely glabrous. Ray florets 40-100, ligulate, white. -
Co-Extinction of Mutualistic Species – an Analysis of Ornithophilous Angiosperms in New Zealand
DEPARTMENT OF BIOLOGICAL AND ENVIRONMENTAL SCIENCES CO-EXTINCTION OF MUTUALISTIC SPECIES An analysis of ornithophilous angiosperms in New Zealand Sandra Palmqvist Degree project for Master of Science (120 hec) with a major in Environmental Science ES2500 Examination Course in Environmental Science, 30 hec Second cycle Semester/year: Spring 2021 Supervisor: Søren Faurby - Department of Biological & Environmental Sciences Examiner: Johan Uddling - Department of Biological & Environmental Sciences “Tui. Adult feeding on flax nectar, showing pollen rubbing onto forehead. Dunedin, December 2008. Image © Craig McKenzie by Craig McKenzie.” http://nzbirdsonline.org.nz/sites/all/files/1200543Tui2.jpg Table of Contents Abstract: Co-extinction of mutualistic species – An analysis of ornithophilous angiosperms in New Zealand ..................................................................................................... 1 Populärvetenskaplig sammanfattning: Samutrotning av mutualistiska arter – En analys av fågelpollinerade angiospermer i New Zealand ................................................................... 3 1. Introduction ............................................................................................................................... 5 2. Material and methods ............................................................................................................... 7 2.1 List of plant species, flower colours and conservation status ....................................... 7 2.1.1 Flower Colours .............................................................................................................