Vascular Plants of an Unclassified Islet, Cape Brett Peninsula, Northern New Zealand, by E.K. Cameron, P

Total Page:16

File Type:pdf, Size:1020Kb

Vascular Plants of an Unclassified Islet, Cape Brett Peninsula, Northern New Zealand, by E.K. Cameron, P TANE 28,1982 VASCULAR PLANTS OF AN UNCLASSIFIED ISLET, CAPE BRETT PENINSULA, NORTHERN NEW ZEALAND by E.K. Cameron Department of Botany, University of Auckland, Private Bag, Auckland SUMMARY Seventy indigenous and 2 adventive vascular plants taxa are recorded for the "unmodified" islet. Its botanical value exceeds its small size because of the modification of the adjacent Cape Brett Peninsula and nearby islands. INTRODUCTION The islet is situated only a few metres off the northern coastline of Cape Brett Peninsula (Fig. 1). This steep beehive-shaped greywacke islet, less than two hectares in area, supports an excellent cover of indigenous vegetation compared with the adjacent goat (Copra hircus) browsed mainland. Approximately thirty minutes was spent on the islet during a four day botanical survey of Cape Brett Peninsula carried out for the Department of Lands and Survey, Auckland, in June 1980 (Cameron 1980). Time permitted only a single south-west to north-east traverse, returning to the starting point via the north-west littoral. PLANT COMMUNITIES For ease of description four plant associations (Fig. 2) are recognised although it must be remembered that these are by no means distinct as they grade into one another. Area 1: Coastal Rock. The amount of coastal rock on the islet is proportional to the degree of wave exposure and thus the north-eastern side of the islet has the greatest amount of exposed rock. Plants such as Asplenium flaccidum ssp. haurakiense, Samolus repens and the shore lobelia (Lobelia anceps) are frequently found growing in cracks and crevices. Others found here include the N.Z. ice plant (Disphyma australe), glasswort (Salicornia australis) shore groundsel (Senecio lautus), Scirpus nodosus and at the upper level Rhagodia triandra. Area 2: Prostrate Vegetation. The steep (c.50°) exposed northern slopes are carpeted with prostrate shrubs; kowhai (Sophora microphylla), 213 Piercy I 0 214 Melicytus novae-zelandiae and taupata (Coprosma repens) all less than half a metre in height. Underneath and growing through this mat is the twining Muehlenbeckia complexa and the 'succulent' pepper, Peperomia urvilleana. Associated with these plants are; the N.Z. iceplant; the renga lily (Arthropodium cirratum); coastal snow tussock (Chionochloa bromoides) and small ferns (Cheilanthes spp.) Area 3: Shrub development. Found at a similar level to Area 2, on the islet, but less exposed. This increase in shelter has allowed shrub development up to 2-3 m in height. Close to Area 2 ngaio (Myoporum laetum), coastal maire (Nestegis apetala) and kowhai are common; with Melicytus novae-zelandiae fringing the rock-shrub interface. On the south-western side coastal maire is abundant with spreading branches and attaining 2-3 m in height. Karaka (Corynocarpus laevigatas), Coprosma macrocarpa, houpara (Pseudopanax lessonii) and mahoe (Melicytus ramiflorus) are common; tawapou (Planchonella novo- zelandica) is present and the N.Z. jasmine (Parsonsia sp.) tangles through this mixed canopy. Ferns (Asplenium oblongifolium, Phymatodes diversifolium, Doodia media, Polystichum richardii) renga lily and Peperomia urvilleana are common on the loose, steep rocky ground. By the rock-shrub interface, karo (Pittosporum crassifolium) N.Z. flax (Phormium tenax) and coastal snow tussock grow. Fig. 2. Four plant communities of the islet; Cape Brett Peninsula in the background. Area 4: Tree development. The islet is crowned with a small forest 5-6 m tall and is comprised of coastal maire, kohekohe (Dysoxylum spectabile), mapou (Myrsine australis) and tawaroa (Beilschmiedia sp.) Pohutukawa 215 (Metrosideros excelsa) and kanuka (Leptospermum ericoides) emerge through this canopy to about 12 m in height. Hangehange (Geniostoma ligustrifolium), rangiora (Brachyglottis repanda) and Coprosma macrocarpa are common shrubs. The ground here is fairly level, less rocky, and the reasonable soil layer supports several ferns (Adiantum cunninghamii, Asplenium oblongifolium), Gahnia lacera and Astelia banksii. ANNOTATED SPECIES LIST Seventy-two taxa of vascular plants were recorded on the islet (Table 1). During the survey no conscious attempt was made to record all the adventive plants, making this group under-recorded. But it should be noted that the adventive plants were small and insignificant compared with the indigenous vegetation. Synonyms or references are given for the lesser-known name changes, * denotes adventive species. Table 1. Vascular flora of unclassified islet according to plant groups and indigenous o adventive status. Group Indigenous Adventive Totals Ferns 11 . 11 Dicots 45 1 46 Monocots 14 1 15 TOTALS 70 2 72 FILICOPSIDA Polypodiaceae Phymatodes diversifolium Hound's tongue. Abundant terrest rially in shaded sites throughout. Pyrrosia serpens Rupestral by the coast and epiphytic on pohutukawa. Aspleniaceae Asplenium flaccidum subsp. (Brownsey 1977). Occasional on ban haurakiense coastal rock. A. oblongifolium Col. Huruhuru whenua. Common, shaded (A. lucidum) sites throughout. Blechnaceae Doodia media Abundant, especially on the western. sides; shaded sites. Dryopteridaceae Polystichum richardii Frequent on the upper western side Adiantaceae Adiantum cunninghamii Maidenhair. Local, by the top of th< islet. A. hispidulum Rosy maidenhair. Occasional shaded sites. Cheilanthes distans Local, on bare rock between prostrate plants, north-eastern side. Growing by C. sieberi. C. sieberi As for C. distans. Pellaea rotundifolia Local open site near the top of the islet, AKU 11573. 216 Dicotyledones Beilschmiedia sp. Tawaroa (large-leaved tawa). Several trees (5-6 m tall) near summit. Clematis parviflora Clematis. Climbing through shrubs on the south-western side. Peperomia urvilleana Frequent on the shaded rocky slopes throughout. Melicytus novae-zelandiae (Green 1970). Prostrate and common on the steep, exposed north-eastern rock; more upright but less frequent on the less exposed north-western side. M. ramiflorus Mahoe. Occasional in the shrub canopy on the south-western side. Disphyma australe N.Z. iceplant; horokaka. Common on the coastal rock, especially on the northern side. Tetragonia trigyna N.Z. spinach. Local, north-eastern side by prostrate shrubs. Muehlenbeckia australis Single, climbing vine near summit. M. complexa Wire vine. Sprawling mats on steep north-eastern side. Rhagodia triandra Occasional sprawling, rock-shrub interface. Salicomia australis Glasswort. Occasional on coastal rocks. Colli trie he muelleri Local, damp mud near summit. Knightia excelsa Rewarewa. Occasional near summit. Pittosporum crassifolium Karo. Occasional 1-2 m tall, rock- shrub interface, south-western side. Occasional, rock-shrub interface, P. umbellatum south-western side and taller plants (5-6 m) near summit. Kanuka. Common at summit, Leptospermum ericoides individual trees reaching about 12 m tall. Pohutukawa. Only present near Metrosideros excelsa summit, emergent to 12 m tall, 60 cm DBH. M. peforata Occasional, near summit as a small liane. Hoheria populnea Houhere; lacebark. Rare, near summit. Sophora microphylla Kowhai. Common and prostrate on the steep north-eastern side. Corynocarpus laevigatus Kohekohe. Occasional, near summit, 5-6 m tall. Pseudopanax arboreus (Philipson 1965). Whauwhaupaku. Occasional, shrub association, south• western side. P. crassifolius x lessonii Two noticed near the summit P. lessonii Houpara. Common from the rock- shrub interface to about halfway up 217 the mid-face on the south-west* side. Epacridaceae Cyathodes juniperina Mingimingi. Rare, near summit. Sapotaceae Planchonella novo-zelandica Tawapou. Occasional from the n> shrub interface to about halfway the mid-face on the south-west* side, 2-3 m tall. Myrsinaceae Myrsine australis Mapou. Common; from small plant the rock-shrub interface on the soul western side to 5-6 m tall trees near the summit. Oleaceae Nestegis apetala Coastal maire. Frequent, low a spreading on the south-western roc shrub interface, becoming taller a: more erect proceeding up the mi face; attaining 6 m tall and 60 c DBH near the summit. It is absent i the north-eastern side. N. lanceolata White maire. Rare, only near sum mi Loganiaceae Geniostoma ligustrifolium Hangehange. Common understorey near summit. Apocynaceae Parsonsia sp. Kaihua. Climbing through the shrub association on the south-western mi face. Rubiaceae Coprosma arborea A single tree about 5 m tall net summit. C. macrocarpa Karamu. Abundant shrub forming i places the main vegetation cove especially near the sea on the wester side; present also in the underscore near the summit. C. repens Taupata. Common and prostrate o the exposed north-eastern side. Compositae Brachyglottis repanda Rangiora. Frequent in the under storey near the summit, 1-2 m tall. Gnaphalium audax (Drury 1972) Occasional, in ope sites. Hypochoeris radicata* Catsear. Several plants, open site between low vegetation. Olearia furfuracea Akepiro. Occasional; 1-2 m tall shrub on the south-western side near ti rock-shrub interface. Senecio kirkii A single 1.5 m plant with very wide leaves observed by the rock-shrub interface on the south-western side. S. lautus Shore groundsel. Frequent on coastal rock. Primulaceae Samolus repens Common on coastal rock, growing closer to the sea than any other vascular plant. Lobeliaceae Lobelia anceps Shore lobelia. Occasional, coastal rock. Convolvulaceae Dichondra repens Mercury Bay weed. Present among; the prostrate cover on the north eastern side. 218 Gesneriaceae Rhabdothamnus solandri Waiuatua. Rare, near summit. Myoporaceae Myoporum laetum
Recommended publications
  • Towards an Understanding of the Evolution of Violaceae from an Anatomical and Morphological Perspective Saul Ernesto Hoyos University of Missouri-St
    University of Missouri, St. Louis IRL @ UMSL Theses Graduate Works 8-7-2011 Towards an understanding of the evolution of Violaceae from an anatomical and morphological perspective Saul Ernesto Hoyos University of Missouri-St. Louis, [email protected] Follow this and additional works at: http://irl.umsl.edu/thesis Recommended Citation Hoyos, Saul Ernesto, "Towards an understanding of the evolution of Violaceae from an anatomical and morphological perspective" (2011). Theses. 50. http://irl.umsl.edu/thesis/50 This Thesis is brought to you for free and open access by the Graduate Works at IRL @ UMSL. It has been accepted for inclusion in Theses by an authorized administrator of IRL @ UMSL. For more information, please contact [email protected]. Saul E. Hoyos Gomez MSc. Ecology, Evolution and Systematics, University of Missouri-Saint Louis, 2011 Thesis Submitted to The Graduate School at the University of Missouri – St. Louis in partial fulfillment of the requirements for the degree Master of Science July 2011 Advisory Committee Peter Stevens, Ph.D. Chairperson Peter Jorgensen, Ph.D. Richard Keating, Ph.D. TOWARDS AN UNDERSTANDING OF THE BASAL EVOLUTION OF VIOLACEAE FROM AN ANATOMICAL AND MORPHOLOGICAL PERSPECTIVE Saul Hoyos Introduction The violet family, Violaceae, are predominantly tropical and contains 23 genera and upwards of 900 species (Feng 2005, Tukuoka 2008, Wahlert and Ballard 2010 in press). The family is monophyletic (Feng 2005, Tukuoka 2008, Wahlert & Ballard 2010 in press), even though phylogenetic relationships within Violaceae are still unclear (Feng 2005, Tukuoka 2008). The family embrace a great diversity of vegetative and floral morphologies. Members are herbs, lianas or trees, with flowers ranging from strongly spurred to unspurred.
    [Show full text]
  • Asplenium Oblongifolium
    Crop & Food Research Plant-SyNZ, INVERTEBRATE IDENTIFICATION CHART STUDENT LEVEL DEMONSTRATION Shining spleenwort – Asplenium oblongifolium FROND Small white scales on underside of frond, Whitefly adults and white waxy areas with Whitefly nymphs and puparia with white waxy present all year. eggs on underside of frond, present all year. areas on underside of frond, present all year. SUCKING INSECT (Coccoidea) 384 SUCKING INSECT (Aleyrodidae) 494 SUCKING INSECT (Aleyrodidae) 494 White mines on upper side of frond, present all year. FLY (Agromyzidae) 32 Other plant damage symptoms and invertebrates that may be seen LEAVES * Twisted and distorted frond, grey aphids Fern spores webbed together on the under- Fern spores webbed together on the may be present on expanding frond, side of frond and small holes in frond to underside of frond. No holes in frond. symptoms all year. upper side where small ‘towers’ may be Probably present all year. SUCKING INSECT (Aphididae) 991 constructed, probably present most of year. MOTH (Gelechioidea) 861 MOTH (Gelechioidea) 583 Other host associations in the Plant-SyNZ database (September 2003) LEVEL OF EXPERTISE No other host associations recorded in the database * = adventive (alien) species This version is suitable for non-experts. A 10x New associations hand lens is useful, but not essential to confirm The host associations illustrated and listed here are those known when this identification the presence of some invertebrates. Versions of guide was compiled. New host associations are likely to be discovered. If invertebrates and/or plant damage are found that may be a new association, send specimens of the this identification guide that are suitable for insects and plants to experts (botanists and entomologists) and Dr Nicholas Martin, students are available.
    [Show full text]
  • Rethinking Arboreal Heritage for Twenty-First-Century Aotearoa New Zealand
    NATURAL MONUMENTS: RETHINKING ARBOREAL HERITAGE FOR TWENTY-FIRST-CENTURY AOTEAROA NEW ZEALAND Susette Goldsmith A thesis submitted to Victoria University of Wellington in fulfilment of the requirements for the degree of Doctor of Philosophy Victoria University of Wellington 2018 ABSTRACT The twenty-first century is imposing significant challenges on nature in general with the arrival of climate change, and on arboreal heritage in particular through pressures for building expansion. This thesis examines the notion of tree heritage in Aotearoa New Zealand at this current point in time and questions what it is, how it comes about, and what values, meanings and understandings and human and non-human forces are at its heart. While the acknowledgement of arboreal heritage can be regarded as the duty of all New Zealanders, its maintenance and protection are most often perceived to be the responsibility of local authorities and heritage practitioners. This study questions the validity of the evaluation methods currently employed in the tree heritage listing process, tree listing itself, and the efficacy of tree protection provisions. The thesis presents a multiple case study of discrete sites of arboreal heritage that are all associated with a single native tree species—karaka (Corynocarpus laevigatus). The focus of the case studies is not on the trees themselves, however, but on the ways in which the tree sites fill the heritage roles required of them entailing an examination of the complicated networks of trees, people, events, organisations, policies and politics situated within the case studies, and within arboreal heritage itself. Accordingly, the thesis adopts a critical theoretical perspective, informed by various interpretations of Actor Network Theory and Assemblage Theory, and takes a ‘counter-’approach to the authorised heritage discourse introducing a new notion of an ‘unauthorised arboreal heritage discourse’.
    [Show full text]
  • Arthropodium 'Te Puna'
    Arthropodium ‘Te Puna’ Arthropodium cirratum ‘Te Puna’ Height: 40cm Spread: 50cm PART SHADE FULL SHADE DRY CONTAINER ATTRACTIVE GROUND EDGING TOLERANT FOLIAGE COVER FEATURES: •Very hardy and water wise with lush, evergreen foliage. •Dwarf form of a popular landscaping plant. •Suited to difficult dry and/or shady areas. •Billowy white floral stems from spring to summer. SUGGESTED USES: •Mass plant for low maintenance areas. •Adds textural contrast and permanent structure to mixed flower or shrub borders. •Containers, small or narrow spaces. •Edging for paths, drives or retaining walls. •Provides a lush effect around water features and poolside landscaping. •Suitable for coastal regions. CULTURAL CARE Very dry tolerant once established. Low maintenance with no pruning generally required other than to tidy. Feed in spring with a general fertiliser. Removing flower stems as they fade will encourage more to develop. Protect from heavy frost. Mulching is advisable to further reduce long term maintenance. Commonly know as ‘New Zealand Rock Lily’ as it is endemic to this country. It grows - as it’s name suggests - in rocky regions where growing conditions are often less than favourable. It is therefore an ideal solution for dry, shaded sites on slopes or beneath trees - infact most places that are a challenge may be overcome with this attractive and tough contender. Mass plant in difficult sites or create a bright habitat in low light areas using just green, silver and whites by pairing up with other shade loving ornamentals such as Brunnera ‘Jack Frost’, Iberis ‘Winter Glow’, Lamium ‘Snow and Frost’ and the beautiful Hellebore ‘Ivory Prince’..
    [Show full text]
  • Distribution and Chemical Diversity of Cyclotides From
    !"# $%%#&'(&)* $%#)+,()(''-(+)() . .. .(- The Violet Down in a green and shady bed, A modest violet grew; Its stalk was bent, it hung its head As if to hide from view. And yet it was a lovely flower, Its colour bright and fair; It might have graced a rosy bower, Instead of hiding there. Yet thus it was content to bloom, In modest tints arrayed; And there diffused a sweet perfume, Within the silent shade. Then let me to the valley go This pretty flower to see; That I may also learn to grow In sweet humility. Jane Taylor (1783-1824) List of Papers This thesis is based on the following papers, which are referred to in the text by their Roman numerals. I Burman, R., Gruber, C.W., Rizzardi, K., Herrmann, A., Craik, D.J., Gupta, M.P., Göransson, U. (2010) Cyclotide proteins and precursors from the genus Gloeospermum: Filling a blank spot in the cyclotide map of Violaceae. Phytochemistry, 71(1):13-20 II Burman, R., Larsson, S., Yeshak, M.Y., Rosengren, K.J., Craik, D.J., Göransson, U. (2010) Distribution of circular
    [Show full text]
  • Nzbotsoc No 107 March 2012
    NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 107 March 2012 New Zealand Botanical Society President: Anthony Wright Secretary/Treasurer: Ewen Cameron Committee: Bruce Clarkson, Colin Webb, Carol West Address: c/- Canterbury Museum Rolleston Avenue CHRISTCHURCH 8013 Subscriptions The 2012 ordinary and institutional subscriptions are $25 (reduced to $18 if paid by the due date on the subscription invoice). The 2012 student subscription, available to full-time students, is $12 (reduced to $9 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $7.00 each. Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next years subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the June 2012 issue is 25 May 2012. Please post contributions to: Lara Shepherd Museum of New Zealand Te Papa Tongarewa P.O. Box 467 Wellington Send email contributions to [email protected]. Files are preferably in MS Word, as an open text document (Open Office document with suffix “.odt”) or saved as RTF or ASCII. Macintosh files can also be accepted. Graphics can be sent as TIF JPG, or BMP files; please do not embed images into documents.
    [Show full text]
  • I UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE
    UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE BIOLOGIA DEPARTAMENTO DE BOTÂNICA ANDRÉA MACÊDO CORRÊA CITOTAXONOMIA DE REPRESENTANTES DA SUBFAMÍLIA RUBIOIDEAE (RUBIACEAE) NOS CERRADOS DO ESTADO DE SÃO PAULO Tese apresentada ao Instituto de Biologia para obtenção do Título de Doutor em Biologia Vegetal Orientadora: Profª. Drª. Eliana Regina Forni-Martins Campinas 2007 i ii Campinas, 02 de Março de 2007 BANCA EXAMINADORA Drª. Eliana Regina Forni-Martins – Orientadora Drª. Maria Angélica Maciel Martinho Ferreira Drª. Sigrid Luiza Jung Mendaçolli Drª. Neiva Isabel Pierozzi Dr. João Semir Drª. Luiza Sumiko Kinoshita - Suplente ______________________________________ Dr. Ricardo Lombelo - Suplente ______________________________________ Drª. Júlia Yamagishi Costa - Suplente ______________________________________ iii À minha família, de valor inestimável. iv AGRADECIMENTOS Este trabalho foi concluído graças ao apoio e dedicação de várias pessoas, que contribuíram direta ou indiretamente para sua realização. Agradeço então: A Deus; À minha família, Agostinho e Aracilda, meus pais, Araceli e Junior, meus irmãos, Otávio Augusto, meu sobrinho, pelo apoio, mesmo à distância; Ao meu marido Emerson, pelo apoio, companheirismo e auxílio nas coletas no campo; À Drª. Eliana, minha orientadora, que novamente confiou no meu trabalho, ensinando e ajudando em diversos momentos; À Universidade Estadual de Campinas, Instituto de Biologia, Departamento de Botânica, Laboratório de Biossistemática, pela infra-estrutura que possibilitou a realização desse trabalho; Ao curso de Pós-graduação em Biologia Vegetal; À FAPESP (Fundação de Apoio à Pesquisa do Estado de São Paulo), pela bolsa de doutorado concedida e os auxílios fornecidos a Drª. Eliana, possibilitando a realização dessa pesquisa; Ao CNPq (Conselho Nacional de Pesquisa e Desenvolvimento Tecnológico) pelo auxílio concedido a Drª.
    [Show full text]
  • Nestegis Lanceolata
    Nestegis lanceolata COMMON NAME White maire SYNONYMS Olea lanceolata Hook.f.; Gymnelaea lanceolata (Hook.f.) L.A.S.Johnson FAMILY Oleaceae AUTHORITY Nestegis lanceolata (Hook.f.) L.A.S.Johnson FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Close up of fruits, Te Moehau (March). No Photographer: John Smith-Dodsworth ENDEMIC FAMILY No STRUCTURAL CLASS Trees & Shrubs - Dicotyledons NVS CODE NESLAN CHROMOSOME NUMBER 2n = 46 CURRENT CONSERVATION STATUS 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened BRIEF DESCRIPTION Tree bearing pairs of dark green narrow smooth leaves that are pale Adult foliage, Waitakere Ranges. Photographer: green underneath. Leaves 5-9cm long by 1-2.5cm wide. Fruit red, 8-11mm Peter de Lange long, containing a single seed. DISTRIBUTION Endemic. North and South Islands. Widespread and common in the North Island except in the southern part of range (Horowhenua, southern Wairarapa and Wellington areas). Very uncommon in the South Island where it is locally present in the Marlborough Sounds, reaching its southern limit along the Tuamarina River. HABITAT Widespread in coastal to montane forest. Commonly found on steep hill slopes and ridge lines but also can be locally common in riparian forest. As a rule white maire tends to avoid frost-prone habitats and sites that frequently flood. In the northern part of its range it is often found with narrow-leaved maire (Nestegis montana) and black maire (Nestegis cunninghamii). In some parts of eastern Northland it is also found in coastal forest with Nestegis apetala. FEATURES Stout gynodioecious spreading tree up to 20 m tall usually forming a domed canopy; trunk up to c.
    [Show full text]
  • Flora of New Zealand Mosses
    FLORA OF NEW ZEALAND MOSSES BRACHYTHECIACEAE A.J. FIFE Fascicle 46 – JUNE 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 Fife, Allan J. (Allan James), 1951- Flora of New Zealand : mosses. Fascicle 46, Brachytheciaceae / Allan J. Fife. -- Lincoln, N.Z. : Manaaki Whenua Press, 2020. 1 online resource ISBN 978-0-947525-65-1 (pdf) ISBN 978-0-478-34747-0 (set) 1. Mosses -- New Zealand -- Identification. I. Title. II. Manaaki Whenua-Landcare Research New Zealand Ltd. UDC 582.345.16(931) DC 588.20993 DOI: 10.7931/w15y-gz43 This work should be cited as: Fife, A.J. 2020: Brachytheciaceae. In: Smissen, R.; Wilton, A.D. Flora of New Zealand – Mosses. Fascicle 46. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/w15y-gz43 Date submitted: 9 May 2019 ; Date accepted: 15 Aug 2019 Cover image: Eurhynchium asperipes, habit with capsule, moist. Drawn by Rebecca Wagstaff from A.J. Fife 6828, CHR 449024. Contents Introduction..............................................................................................................................................1 Typification...............................................................................................................................................1
    [Show full text]
  • Vascular Flora of Motuora Island, Hauraki Gulf Shelley Heiss-Dunlop & Jo Fillery
    Vascular flora of Motuora Island, Hauraki Gulf Shelley Heiss-Dunlop & Jo Fillery Introduction 1988). A total of 141 species (including 14 ferns) were Motuora Island lies in the Hauraki Gulf southwest of recorded. Exotic plants confined to the gardens Kawau Island, approximately 3km from Mahurangi around the buildings at Home Bay were not included Heads, and 5km from Wenderholm Regional Park, in Dowding’s (1988) list. Dowding (1988) commented Waiwera. This 80ha island is long and narrow on four adventive species that were “well-established” (approximately 2km x c. 600m at its widest) with a and that “may present problems” (presumably for a relatively flat top, reaching 75m asl. The land rises future restoration project). These species were abruptly, in places precipitously, from the shoreline so boneseed (Chrysanthemoides monilifera), boxthorn that the area of the undulating ‘level’ top is (Lycium ferocissimum), gorse (Ulex europaeus) and comparatively extensive. Composed of sedimentary kikuyu grass (Pennisetum clandestinum). All four strata from the Pakiri formation of the Waitemata species still require ongoing control. However, as a Group (Lower Miocene age, approximately 20 million years old), Motuora is geologically similar to other result of ongoing weed eradication endeavours, inner Hauraki gulf islands such as Tiritiri Matangi, boxthorn has been reduced to a few isolated sites, Kawau, Waiheke and Motuihe Islands (Ballance 1977; and boneseed once widespread on the island is Edbrooke 2001). considerably reduced also, occurring in high densities now only on the northern end of the island (Lindsay History 2006). Gorse and kikuyu are controlled where these Motuora Island was farmed, from as early as 1853 species inhibit revegetation plantings.
    [Show full text]
  • A Multi-Gene Region Targeted Capture Approach to Detect Plant DNA in Environmental Samples
    bioRxiv preprint doi: https://doi.org/10.1101/2021.07.03.450983; this version posted July 26, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 A multi-gene region targeted capture approach to detect plant DNA in 2 environmental samples: A case study from coastal environments 3 Nicole R. Foster1*, Kor-jent van Dijk1, Ed Biffin2, Jennifer M. Young3, Vicki Thomson1, 4 Bronwyn M. Gillanders1, Alice Jones1,4, Michelle Waycott1,2 5 6 Abstract 7 Metabarcoding of plant DNA recovered from environmental samples, termed environmental DNA 8 (eDNA), has been used to detect invasive species, track biodiversity changes and reconstruct past 9 ecosystems. The P6 loop of the trnL intron is the most widely utilized gene region for metabarcoding 10 plants due to the short fragment length and subsequent ease of recovery from degraded DNA, which 11 is characteristic of environmental samples. However, the taxonomic resolution for this gene region is 12 limited, often precluding species level identification. Additionally, targeting gene regions using 13 universal primers can bias results as some taxa will amplify more effectively than others. To increase 14 the ability of DNA metabarcoding to better resolve flowering plant species (angiosperms) within 15 environmental samples, and reduce bias in amplification, we developed a multi-gene targeted capture 16 method that simultaneously targets 20 chloroplast gene regions in a single assay across all flowering 17 plant species.
    [Show full text]
  • 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.
    [Show full text]