Woody Vegetation in the Upland Region of Rarotonga, Cook Islands!

Total Page:16

File Type:pdf, Size:1020Kb

Woody Vegetation in the Upland Region of Rarotonga, Cook Islands! Pacific Science (1985), vol. 39, no. 1 © 1985 by the University ofHawaii Press. All rights reserved Woody Vegetation in the Upland Region of Rarotonga, Cook Islands! MARK D. MERLIN2 2 ABSTRACT: Rarotonga is the largest (64 km ) and by far the highest (652 m) of the Cook Islands. The native coastal and lowland vegetation of this high volcanic, tropical island has been either completely removed or heavily disturbed. Numerous exotic plant species have been introduced and many ofthese are now naturalized in the lower elevation habitats ofthe island. The results ofthis initial, quantitative study in the upland forests ofRarotonga indicate, however, that the plant life ofthe rugged interior is still largely dominated by native species. Over 92 percent of all the woody plants (dbh > 2.5 cm) sampled in the 19 upland forest transects are either indigenous or endemic to Rarotonga. Native plants also accounted for more than 95 percent ofthe basal area covered by the woody vegetation in the upland study area. Three basic native plant associations have been recognized by dendrogram analysis: (1) the Homalium montane forest; (2) the Fagraea-Fitchia ridge forest; and (3) the Metrosideros cloud forest. The first two associations develop under subtropical climatic conditions, while the cloud forest is adapted to warm temperate conditions. Some aspects of the biogeo­ graphical significance ofthis unique forest region and the ecological implications of human disturbance in the uplands are also discussed. THE COOK ISLANDS INCLUDE fifteen small coral that both vegetation and floristic research in and volcanic islands with a total land area of the island group have been quite limited. approximately 238 km2 scattered over about Rarotonga is the only island in the Cook Ar­ 2,176,000 km2 of the South Pacific Ocean chipelago with two published floras (Cheese­ between 9° and 23° S latitude and 156° and man 1903, Wilder 1931); but the most recent 167° W longitude (see Figure 1). Rarotonga, of these, over 50 years old, has a number of located near the southern end of the archi­ inaccuracies and needs considerable updating pelago at 21° 12' S latitude and 158° 46' W (Sykes 1980, W. Authur Whistler, pers. 2 longitude, is the largest (64 km ) and by far comm. 1984). In addition to Sykes' literature the highest (652 m) of the Cook Islands (Fig­ review, the only recent botanical publications ure 1). This island is the subaerial portion of dealing with Rarotonga include a brief flo­ an extinct shield volcano typical of the ig­ ristic discussion emphasizing phytogeography neous formations commonly found in the (Philipson 1971), a taxonomic account of the deep Pacific Ocean Basin. ferns and fern allies found in the Southern In his annotated bibliographic study of Cook Islands (Brownlie and Philipson 1971), botanical research carried out in the Cook and a list of the vascular flora on the reef Islands, Sykes (1980) briefly described the veg­ islands of Rarotonga (Fosberg 1972). etation of the Cook Islands and presented an In an unpublished, descriptive report based exhaustive survey of the references to the ter­ on field work carried out in 1974 and 1975, restrial plant life in the archipelago. He notes Sykes (1976, revised in 1983) divided the veg­ etation of Rarotonga into coastal, lowland, and upland zones. The coastal zone, which 1 Manuscript accepted 15 August 1984. 2 University of Hawaii at Manoa, General Science contains strand, scrub, and small makatea Department, Honolulu, Hawaii 96822. (raised limestone) components, still has some 81 82 PACIFIC SCIENCE, Volume 39, January 1985 VEGETATION SAMPLING SITES ON RAROTONGA 21 15' tienrhyn o M.~nihikj Pukapuk.t c;;) Nass.u 0 NORTHERN GROUP Suwarrow Is. o 160 W 180 140 W Hawaii 20 N COOK ISLANDS • Sampling Siles PACIFIC Equ.lor.J. + --J-.oPa~~rlston Paved Roads OCEAN Aitutaki 0 ~bnU~itiIIrO ----0 Sireams Til ulea 0 l) 20 Aliu ~auke L!. Mln.,Peaks Q NGAo Coral Reef Mangaia "'",w SOUTHE N GROUP Towns Tropic f C.pricorn L-_'-'.!_4---o'{,,2__--" Mile Q 1{2 1 Kilometer Miles 0 100 200 ]90 Kilometers 0 100 200 ]00 400500 FIGURE 1. Map of the Cook Islands and vegetation sampling sites on Rarotonga. Woody Vegetation in,Upland Rarotonga-MERLIN 83 FIGURE 2. The northern coast, lowlands, and lower uplands of Rarotonga, areas (e,g., the Muri Sand) where native vege­ Numerous introduced species have become tation can be found. However, the majority of naturalized along the coast orin the lowlands. this zone has been greatly modified by human Some of these nonnative plants were brought disturbance. The native plants that can still be in during the prehistoric Polynesian period, found in this zone, such as Ipomoea pes­ but many more were introduced after the caprae, Vigna marina, Scaevola taccada, Bar­ initial European contact in the early part of ringtonia asiatica, Hernandia nymphaeifolia, the 19th century. and Pisonia grandis, are almost all organisms Weedy plants that have become abundant commonly found in the coastal areas of trop­ in some parts of the lower habitats of Raro­ ical South Pacific islands. tonga include herbaceous species such as The lowland vegetation zone of Raro­ Bidens pilosa, Elephantopus mollis, Euphorbia tonga comprises the low lying, generally level hirta, Mimosa pudica, Sida rhombifolia, area located between the coastal coral sands Mikania micrantha, Momordica charantia, and the steep hills a few hundred meters in­ Panicum maximum, Chrysopogon aciculatus, land. This zone also includes the lower, mode­ Cenchrus echinatus, Sorghum bicolor, and rately inclined, hilly areas near the coast and Stenotaphrum secundatum. Exotic woody the valley bottoms which, in some places, species that are commonly naturalized in penetrate far into the interior of the island some coastal or lowland habitats include (Figure 2). Although this zone contains the Leucaena leucocephala, Lantana camara, most fertile soils on Rarotonga, almost all of Aleurites moluccana, Inocarpus fagifer, Man­ the original lowland plant life of Rarotonga gifera indica, Cecropia palmata, Inga edulis, has been replaced by exotic associations of Syzygium sp., Psidium guajava, and more re­ cultivated and/or weedy plants (Figure 3). cently Ardisia humilis. It should also be noted 84 PACIFIC SCIENCE, Volume 39, January 1985 FIGURE 3. Cultivated pondfields and plantations in lower Takuvaine Valley, with Ikurangi Peak in the far background. that Hibiscus tiliaceus, an aggressive, woody both start atlower elevations on the windward species which is commonly found along some side of the island. coastal areas, in abandoned plantations and These upland vegetation subzones of taro (Colocasia esculenta) pondfields, on Rarotonga are botanically unique and of stream banks (Figure 4), and even in some of special scientific interest for two reasons: (I) the more recently disturbed lower forest as noted above and supported in the present slopes, is here considered to be an early Poly­ study, these subzones are still almost entirely nesian introduction in the Cook Islands (cf. covered by native species; and (2) since the Fosberg 1975). summit ofMangaia, the second highest island Unlike the vegetation in the coastal and in the Cook group, is only 168 m (550 ft) lowland zones on Rarotonga that is predomi­ above sea level, the native vegetation above nately exotic, the plant life found in the rugged about 200 m on Rarotonga is not, or in many uplands is overwhelmingly made up ofnative cases may never have been, found anywhere species (Cheeseman 1903, Philipson 1971, else in the Cook Islands. Consequently, the Sykes 1980). This upland zone includes all of native upland forests of Rarotonga can only the interior area above about 50 m to 200 m be compared with similar native subtropical (Figure 5). Itcan be separated into subtropical and warm temperate ecosystems found on and warm temperate subzones which have dis­ other high volcanic islands in: (1) the Society, tributions that vary widely according to the Marquesas, and Austral islands located altitude and aspect ofthe narrow ridges, steep hundreds of kilometers to the east; (2) the slopes, and deep valleys. Thus, for example, Samoan, Tongan, and Fijian islands located the subtropical and warm temperate subzones hundreds of kilometers to the west; or (3) in Woody Vegetation in Upland Rarotonga-MERLIN 85 FIGURE 4. Hibiscus tiliaceus and native ferns on the banks ofPapua Stream. FIGURE 5. The uplands in the interior of Rarotonga, with Maungaroa (509 m) the highest peak in this east-facing view. 86 PACIFIC SCIENCE, Volume 39, January 1985 the Kermadec Islands and part of the North posits. These are bordered by a small fringing Island of New Zealand farther to the reef that encloses a narrow lagoon. southwest. Although Rarotonga lies in the path of the In spite of the unique environmental situa­ generally mild, prevailing southeast trade­ tion and nearly original condition ofthe native winds, it is periodically affected by severe tro­ upland forests of Rarotonga, there have been pical storm or cyclone conditions during the no previous detailed ecological studies of this warmer, more humid hurricane season that region (Sykes 1980). The nearly pristine eco­ usually lasts from November to April. In the logy, exceptional phytogeography, and lack lowlands ofthe island, the mean monthly tem­ of any prior quantitative vegetation research perature ranges from 22° C in July to 26° C in in the central part ofthe island have prompted January, a difference of only 4° C (Kennedy this study ofthe woody vegetation in the sub­ 1974). The average annual rainfall in the tropical and warm temperate uplands of coastal lowlands is 2ll0mm. A large percen­ Rarotonga. The major aims of this research tage ofthe yearly precipitation usually occurs are to determine what kinds of woody plant during the summer months of the Southern associations occur in these uplands, to mea­ Hemisphere (especially December-March) sure the relative dominance and frequency of when the tradewinds are more variable and the individual species found in these vege­ the island may experience squalls and north­ tation types, and to quantify the extent to erly winds (Stoddart 1975).
Recommended publications
  • ATIU SWIFTLET KOPEKA (Aerodramus Sawtelli): SPECIES STATUS REPORT 2020
    ATIU SWIFTLET KOPEKA (Aerodramus sawtelli): SPECIES STATUS REPORT 2020 Atiu Swiftlet James J. S. Johnson Author: Te Ipukarea Society Te Ipukarea Society, PO Box 649, Rarotonga Cook Islands Funded with the support of: The Ridge to Reef Project through the National Environment Service, funded by Global Environment Facility (GEF) and facilitated by United Nations Development Programme (UNDP) Species status report – Kopeka, Atiu Swiftlet (Aerodramus sawtelli) Summary The Atiu swiftlet (Aerodramus sawtelli), known locally as the kopeka, is endemic to the island of Atiu within the Cook Islands and is listed under the IUCN Red List as ‘Vulnerable’ (BirdLife International, 2016; IUCN 2020). Under the Ridge to Reef project (R2R), the Atiu Swiftlet was listed as a key terrestrial species for conservation activities (UNDP Project document, undated). Projects relevant to the kopeka that were initially planned to be implemented under R2R included: support for the kopeka conservation effort; support collaborative work amongst key stakeholders such as National Environment Service (NES), National Heritage Trust (NHT), the Atiu Island Council and Traditional Leaders to create and implement a Species Conservation Plan for this species; and to measure the population at the end of the project to gauge the overall results of the species conservation plan. The R2R baseline figures for the kopeka were recorded at 420 individuals in 2015. Species target goals upon completion of the R2R project were for ‘no net decline in population numbers’. During the four-year R2R programme 2015-19, later extended to 2021, no updated population surveys were conducted. In 2016 -2017, estimated population numbers were around 600 adults (M.
    [Show full text]
  • Coreopsideae Daniel J
    Chapter42 Coreopsideae Daniel J. Crawford, Mes! n Tadesse, Mark E. Mort, "ebecca T. Kimball and Christopher P. "andle HISTORICAL OVERVIEW AND PHYLOGENY In a cladistic analysis of morphological features of Heliantheae by Karis (1993), Coreopsidinae were reported Morphological data to be an ingroup within Heliantheae s.l. The group was A synthesis and analysis of the systematic information on represented in the analysis by Isostigma, Chrysanthellum, tribe Heliantheae was provided by Stuessy (1977a) with Cosmos, and Coreopsis. In a subsequent paper (Karis and indications of “three main evolutionary lines” within "yding 1994), the treatment of Coreopsidinae was the the tribe. He recognized ! fteen subtribes and, of these, same as the one provided above except for the follow- Coreopsidinae along with Fitchiinae, are considered ing: Diodontium, which was placed in synonymy with as constituting the third and smallest natural grouping Glossocardia by "obinson (1981), was reinstated following within the tribe. Coreopsidinae, including 31 genera, the work of Veldkamp and Kre# er (1991), who also rele- were divided into seven informal groups. Turner and gated Glossogyne and Guerreroia as synonyms of Glossocardia, Powell (1977), in the same work, proposed the new tribe but raised Glossogyne sect. Trionicinia to generic rank; Coreopsideae Turner & Powell but did not describe it. Eryngiophyllum was placed as a synonym of Chrysanthellum Their basis for the new tribe appears to be ! nding a suit- following the work of Turner (1988); Fitchia, which was able place for subtribe Jaumeinae. They suggested that the placed in Fitchiinae by "obinson (1981), was returned previously recognized genera of Jaumeinae ( Jaumea and to Coreopsidinae; Guardiola was left as an unassigned Venegasia) could be related to Coreopsidinae or to some Heliantheae; Guizotia and Staurochlamys were placed in members of Senecioneae.
    [Show full text]
  • Cook Islands of the Basicbasic Informationinformation Onon Thethe Marinemarine Resourcesresources Ofof Thethe Cookcook Islandsislands
    Basic Information on the Marine Resources of the Cook Islands Basic Information on the Marine Resources of the Cook Islands Produced by the Ministry of Marine Resources Government of the Cook Islands and the Information Section Marine Resources Division Secretariat of the Pacific Community (SPC) with financial assistance from France . Acknowledgements The Ministry of Marine Resources wishes to acknowledge the following people and organisations for their contribution to the production of this Basic Information on the Marine Resources of the Cook Islands handbook: Ms Maria Clippingdale, Australian Volunteer Abroad, for compiling the information; the Cook Islands Natural Heritage Project for allowing some of its data to be used; Dr Mike King for allowing some of his drawings and illustration to be used in this handbook; Aymeric Desurmont, Secretariat of the Pacific Community (SPC) Fisheries Information Specialist, for formatting and layout and for the overall co-ordination of efforts; Kim des Rochers, SPC English Editor for editing; Jipé Le-Bars, SPC Graphic Artist, for his drawings of fish and fishing methods; Ministry of Marine Resources staff Ian Bertram, Nooroa Roi, Ben Ponia, Kori Raumea, and Joshua Mitchell for reviewing sections of this document; and, most importantly, the Government of France for its financial support. iii iv Table of Contents Introduction .................................................... 1 Tavere or taverevere ku on canoes ................................. 19 Geography ............................................................................
    [Show full text]
  • Chromosome Numbers in Compositae, XII: Heliantheae
    SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII.
    [Show full text]
  • New Insights on Bidens Herzogii (Coreopsideae, Asteraceae), an Endemic Species from the Cerrado Biogeographic Province in Bolivia
    Ecología en Bolivia 52(1): 21-32. Mayo 2017. ISSN 1605-2528. New insights on Bidens herzogii (Coreopsideae, Asteraceae), an endemic species from the Cerrado biogeographic province in Bolivia Novedades en el conocimiento de Bidens herzogii (Coreopsideae, Asteraceae), una especie endémica de la provincia biogeográfica del Cerrado en Bolivia Arturo Castro-Castro1, Georgina Vargas-Amado2, José J. Castañeda-Nava3, Mollie Harker1, Fernando Santacruz-Ruvalcaba3 & Aarón Rodríguez2,* 1 Cátedras CONACYT – Centro Interdisciplinario de Investigación para el Desarrollo Integral Regional, Unidad Durango (CIIDIR-Durango), Instituto Politécnico Nacional. 2 Herbario Luz María Villarreal de Puga (IBUG), Instituto de Botánica, Departamento de Botánica y Zoología, Universidad de Guadalajara. Apartado postal 1-139, Zapopan 45101, Jalisco, México. *Author for correspondence: [email protected] 3 Laboratorio de Cultivo de Tejidos, Departamento de Producción Agrícola, Universidad de Guadalajara. Apartado postal 1-139, Zapopan 45101, Jalisco, México. Abstract The morphological limits among some Coreopsideae genera in the Asteraceae family are complex. An example is Bidens herzogii, a taxon first described as a member of the genus Cosmos, but recently transferred to Bidens. The species is endemic to Eastern Bolivia and it grows on the Cerrado biogeographic province. Recently collected specimens, analysis of herbarium specimens, and revisions of literature lead us to propose new data on morphological description and a chromosome counts for the species, a tetraploid, where x = 12, 2n = 48. Lastly, we provide data on geographic distribution and niche modeling of B. herzogii to predict areas of endemism in Eastern Bolivia. This area is already known for this pattern of endemism, and the evidence generated can be used to direct conservation efforts.
    [Show full text]
  • National Fishery Sector Overview Cook Islands
    FISHERY AND AQUACULTURE Food and Agriculture COUNTRY PROFILE Organization of the United FID/CP/COK Nations PROFIL DE LA PÊCHE ET DE Organisation des Nations Unies L’AQUACULTURE PAR PAYS pour l'alimentation et l'agriculture RESUMEN INFORMATIVO SOBRE Organización de las Naciones May 2010 LA PESCA Y LA ACUICULTURA POR Unidas para la Agricultura y la PAÍSES Alimentación NATIONAL FISHERY SECTOR OVERVIEW COOK ISLANDS 1. GENERAL GEOGRAPHIC AND ECONOMIC DATA Area: 237 km² Water area: 1 830 000 km² Shelf area: [no continental shelf] Length of continental coastline: 419 km (length of the coast of islands) Population (2007)*: 20 000 GDP at purchaser's value (2008) 225 676 000 USD1 GDP per head (2008): 10 645 USD Agricultural GDP (2008): 17 172 000 USD2 Fisheries GDP (2007): 3 318 000 USD3 * source: UN Population Division) 2. FISHERIES DATA Total Per Caput 2007 Production Imports Exports Supply Supply tonnes liveweight kg/year Fish for direct human 2 056 351 1 259 1 148 57.4 consumption4 1 2007 average exchange rate: US$1 – New Zealand $1.36; GDP source: A summary of the national accounts of the Cook Islands is given in Statistics Office (2008). Economic Statistics. Available at www.stats.gov.ck/Statistics/Economic. Staff of the Statistics Office kindly provided a disaggregation of the “agriculture and fishing” component, from which the fishing contribution to GDP can be determined. 2 This is the official contribution of agriculture to GDP and does not include fishing. 3 This is the official fishing contribution to GDP. A recalculation shows the total fishing contribution to be USD$2.9 million: Gillett (2009).
    [Show full text]
  • Tuhinga Pdf for TPP:Layout 1
    Tuhinga 21: 99–123 Copyright © Museum of New Zealand Te Papa Tongarewa (2010) Rediscovering the collection: Cook Islands material culture in the Museum of New Zealand Te Papa Tongarewa Grace Hutton*, Safua Akeli** and Sean Mallon*** * Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, New Zealand ([email protected]) ** Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, New Zealand ([email protected]) *** Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, New Zealand ([email protected]) ABSTRACT: Artefacts from the Cook Islands have been collected since the Museum of New Zealand Te Papa Tongarewa (Te Papa) opened in 1865 as the Colonial Museum. In this article we provide a historical overview of the Cook Islands collection at Te Papa. We discuss the strengths and weaknesses of the collection, review some of the factors influencing its growth, and consider the possibilities for future collection development. This article is an output of a survey of the Cook Islands collection carried out between 2007 and 2009. KEYWORDS: Te Papa, Cook Islands collection, Pacific Cultures collection, Pacific Islanders, New Zealand, museums. Introduction to New Zealand in recent decades. What began in the It is only since 1993 that the Museum of New Zealand Te nineteenth century as a comparative collection of ethno - Papa Tongarewa (Te Papa) has managed its Pacific treasures graphic ‘specimens’ – objects collected during the scientific as a separate collection. For most of the institution’s history study of peoples and cultures – has broadened to include (as the Colonial Museum from 1865 to 1907, the Dominion contemporary works by known artists.
    [Show full text]
  • Treaty Between the United States of America and the Cook Islands (1980)
    TREATIES AND OTHER INTERNATIONAL ACTS SERIES 10774 MARITIME BOUNDARIES Treaty Between the UNITED STATES OF AMERICA and the COOK ISLANDS Signed at Rarotonga June 11, 1980 NOTE BY THE DEPARTMENT OF STATE Pursuant to Public Law 89-497, approved July 8, 1966 (80 Stat. 271; 1 U.S.C. 113)- "... the Treaties and Other International Acts Series issued under the authority of the Secretary of State shall be competent evidence . of the treaties, international agreements other than treaties, and proclamations by the President of such treaties and international agree- ments other than treaties, as the case may be, therein contained, in all the courts of law and equity and of maritime jurisdiction, d in all the tribunals and public offices of the United States, and of the several States, without any further proof or authentication thereof." For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 COOK ISLANDS Maritime Boundaries Treaty signed at Rarotonga June 11, 1980; Transmitted by the President of the United States of America to the Senate September 2, 1980 (S. Ex. P, 96th Cong., 2d Sess.); Reported favorably by the Senate Committee on Foreign Rela­ tions February 11, 1982 (S. Ex. Rept. No. 97­49, 97th Cong., 2d Sess.); Advice and consent to ratification by the Senate June 21, 1983; Ratified by the President August 16, 1983; Ratified by the Cook Islands September 8, 1983; Ratifications exchanged at Rarotonga September 8, 1983; Proclaimed by the President October 31, 1983; Entered into force September 8,
    [Show full text]
  • Activite Anti-Age De L'extrait De Fitchia Nutans, Un Ingredient
    C. R. Chimie xxx (2016) 1e7 Contents lists available at ScienceDirect Comptes Rendus Chimie www.sciencedirect.com Full paper/Memoire Activite anti-age^ de l'extrait de Fitchia nutans, un ingredient cosmeticeutique d'un monoï traditionnel polynesien Anti-ageing activity of Fitchia nutans extract, a cosmeticeutical ingredient of a Polynesian traditional monoï Jean-Luc Ansel a, b, Quoc Ly a, Jean-François Butaud c, Mael Nicolas a, d, Gaetan€ Herbette e, Laurent Peno-Mazzarino f, Elian Lati f, * Phila Raharivelomanana a, a EIO, UMR 241, universite de la Polynesie française, BP 6570, 98702 Faa'a, Tahiti, France b Cosmetic-Valley, 1, place de la Cathedrale, 28200 Chartres, France c Consultant en foresterie et botanique polynesienne, BP 52832, 98716 Pirae, Tahiti, France d Geoazur, UMR 7329, Universite de NiceeSophia Antipolis, 250, rue Albert-Einstein, Sophia Antipolis, 06560 Valbonne, France e Spectropole, FR 1739, Universite Aix-Marseille, Campus Saint-Jerome,^ 13397 Marseille cedex 20, France f Laboratoire BIO-EC, 1, chemin de Saulxier, 91160 Longjumeau, France article info résumé Article history: Fitchia nutans (asterac ee), plante d'un genre endemique de Polynesie française, autrefois Received 17 December 2015 utilisee traditionnellement pour les soins de la peau comme ingredient des monoï sacres, Accepted 8 March 2016 fait partie de la cosmetop ee polynesienne. Les extraits de feuille de F. nutans ont et e soumis Available online xxxx a des tests d'activite anti-age,^ sur explants de peau ex vivo montrant leurs potentialites a Mots-cles: stimuler la croissance de collagene et d'elastine dermique. L'etude phytochimique de cette Fitchia nutans plante, realisee pour la premiere fois, montre que les constituants principaux sont des Activite anti-age^ sesquiterpenoïdes (incluant un nouveau produit naturel, le 15-isovaleroyloxydihydro- Test ex vivo sur peau costunolide), des phenylpropanoïdes et des composes phenoliques.
    [Show full text]
  • Supplementary Material Saving Rainforests in the South Pacific
    Australian Journal of Botany 65, 609–624 © CSIRO 2017 http://dx.doi.org/10.1071/BT17096_AC Supplementary material Saving rainforests in the South Pacific: challenges in ex situ conservation Karen D. SommervilleA,H, Bronwyn ClarkeB, Gunnar KeppelC,D, Craig McGillE, Zoe-Joy NewbyA, Sarah V. WyseF, Shelley A. JamesG and Catherine A. OffordA AThe Australian PlantBank, The Royal Botanic Gardens and Domain Trust, Mount Annan, NSW 2567, Australia. BThe Australian Tree Seed Centre, CSIRO, Canberra, ACT 2601, Australia. CSchool of Natural and Built Environments, University of South Australia, Adelaide, SA 5001, Australia DBiodiversity, Macroecology and Conservation Biogeography Group, Faculty of Forest Sciences, University of Göttingen, Büsgenweg 1, 37077 Göttingen, Germany. EInstitute of Agriculture and Environment, Massey University, Private Bag 11 222 Palmerston North 4474, New Zealand. FRoyal Botanic Gardens, Kew, Wakehurst Place, RH17 6TN, United Kingdom. GNational Herbarium of New South Wales, The Royal Botanic Gardens and Domain Trust, Sydney, NSW 2000, Australia. HCorresponding author. Email: [email protected] Table S1 (below) comprises a list of seed producing genera occurring in rainforest in Australia and various island groups in the South Pacific, along with any available information on the seed storage behaviour of species in those genera. Note that the list of genera is not exhaustive and the absence of a genus from a particular island group simply means that no reference was found to its occurrence in rainforest habitat in the references used (i.e. the genus may still be present in rainforest or may occur in that locality in other habitats). As the definition of rainforest can vary considerably among localities, for the purpose of this paper we considered rainforests to be terrestrial forest communities, composed largely of evergreen species, with a tree canopy that is closed for either the entire year or during the wet season.
    [Show full text]
  • Genetic Diversity and Evolution in Lactuca L. (Asteraceae)
    Genetic diversity and evolution in Lactuca L. (Asteraceae) from phylogeny to molecular breeding Zhen Wei Thesis committee Promotor Prof. Dr M.E. Schranz Professor of Biosystematics Wageningen University Other members Prof. Dr P.C. Struik, Wageningen University Dr N. Kilian, Free University of Berlin, Germany Dr R. van Treuren, Wageningen University Dr M.J.W. Jeuken, Wageningen University This research was conducted under the auspices of the Graduate School of Experimental Plant Sciences. Genetic diversity and evolution in Lactuca L. (Asteraceae) from phylogeny to molecular breeding Zhen Wei Thesis submitted in fulfilment of the requirements for the degree of doctor at Wageningen University by the authority of the Rector Magnificus Prof. Dr A.P.J. Mol, in the presence of the Thesis Committee appointed by the Academic Board to be defended in public on Monday 25 January 2016 at 1.30 p.m. in the Aula. Zhen Wei Genetic diversity and evolution in Lactuca L. (Asteraceae) - from phylogeny to molecular breeding, 210 pages. PhD thesis, Wageningen University, Wageningen, NL (2016) With references, with summary in Dutch and English ISBN 978-94-6257-614-8 Contents Chapter 1 General introduction 7 Chapter 2 Phylogenetic relationships within Lactuca L. (Asteraceae), including African species, based on chloroplast DNA sequence comparisons* 31 Chapter 3 Phylogenetic analysis of Lactuca L. and closely related genera (Asteraceae), using complete chloroplast genomes and nuclear rDNA sequences 99 Chapter 4 A mixed model QTL analysis for salt tolerance in
    [Show full text]
  • A Grammar of the Manihiki Language
    A Grammar of the Manihiki Language Aslak Vaag Olesen BA (Aarhus), MA (Copenhagen) A thesis submitted in fulfilment of the requirements for the degree of Master of Philosophy (MPhil) in Linguistics School of Humanities and Social Science Faculty of Education and Arts University of Newcastle, NSW, Australia July 2020 I hereby certify that the work embodied in the thesis is my own work, conducted under normal supervision. The thesis contains no material which has been accepted, or is being examined, for the award of any other degree or diploma in any university or other tertiary institution and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made. I give consent to the final version of my thesis being made available worldwide when deposited in the University’s Digital Repository, subject to the provisions of the Copyright Act 1968 and any approved embargo. Signature: Date: i Dedications To Norwegian adventurer Thor Heyerdahl, For igniting my life-long interest in Polynesia through his writings. To Professor William Wilson of the University of Hawai‘i, For suggesting to me to make the language of Manihiki and Rakahanga the object of this present work. To all the people of Manihiki and Rakahanga, For generously sharing their time and their knowledge with me, and for inviting me into their homes and treating me like an old friend. And to my partner, Gabrielle McGinnis, For being a constant support for me through all the ups and downs that I have encountered during my travels in the Pacific and during the writing of this thesis.
    [Show full text]