FIJI – Country Data Dossier for Reducing Risk of Extinction Summary Sheet
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Pelagodoxa Henryana (Arecaceae): a Supplement of Additional Photographs and Figures to the 2019 Article in the Journal PALMS
PALMARBOR Hodel et al.: Pelagodoxa supplement 2019-1: 1-24 Pelagodoxa henryana (Arecaceae): A Supplement of Additional Photographs and Figures to the 2019 Article in the Journal PALMS DONALD R. HODEL, JEAN-FRANCOIS BUTAUD, CRAIG E. BARRETT, MICHAEL H. GRAYUM, JAMES KOMEN, DAVID H. LORENCE, JEFF MARCUS, AND ARIITEUIRA FALCHETTO With its large, initially undivided leaves; big, curious, warty fruits; monotypic nature; and mysterious, remote, island habitat, Pelagodoxa henryana has long fascinated palm botanists, collectors and growers, and been one of the holy grails of all who have an interest in palms. The possibility of a second species of Pelagodoxa has generated a substantial amount of interest but the recent literature on the subject has dismissed this prospect and accepted or recognized only one species. However, for 40 years the senior author has propagated and grown P. henryana nearly side by side with a second species of the genus, first in Hawaii, U.S.A and later at his wife’s home in Papeari, Tahiti, French Polynesia, allowing ample opportunity to compare and contrast the two species at various stages of development. An article we wrote reassessing the genus Pelagodoxa was published in the journal PALMS [Hodel et al., Reassessment of Pelagodoxa, PALMS 63(3): 113-146. 2019]. In it we document substantial and critical differences between the two species, P. henryana and P. mesocarpa, establish the validity and resurrect the name of the second species from synonymy, discuss molecular data, phylogeny and phytogeography, ethnobotany and conservation of Pelagodoxa and what impact, if any, they might have had in its speciation and insular distribution. -
Promecothecini Chapuis 1875 Promecothecites Chapuis 1875:300
Tribe Promecothecini Chapuis 1875 Promecothecites Chapuis 1875:300. Handlirsch 1925:666 (classification); Gressitt 1950:81 (China species). Promecothecini Chapuis. Würmli 1975a:45 (genera); Bouchard et al. 2011:78, 518 (nomenclature); Liao et al. 2015:162 (host plants). Promecothecini Weise 1911a:78. Weise 1911b:81 (redescription); Zacher 1913:103 (key); Handlirsch 1925:666 (classification); Uhmann 1931i:848 (museum list), 1940g:121 (claws), 1951a:31 (museum list), 1958e:222 (catalog), 1959d:8 (scutellum), 1964a:458 (catalog), 1964(1965):241 (faunal list), 1966d:275 (note); Bryant 1936:256 (faunal list); Liu 1936:249 (China species); Wu 1937:912 (faunal list); Gressitt 1939c:133 (distribution), 1957b:279 (South Pacific species), 1970:71 (Fiji species); Gressitt & Kimoto 1963a:905 (China species); Seeno & Wilcox 1982:164 (catalog); Jolivet 1988b:13 (host plants), 1989b:310 (host plants); Jolivet & Hawkeswood 1995:154 (host plants); Cox 1996a:172 (pupae); Mohamedsaid 2004:169 (Malaysian species); Staines 2004a:317 (host plants); Chaboo 2007:183 (phylogeny). Type genus:Promecotheca Blanchard. Promecispa Weise 1909 Promecispa Weise 1909:112. Type species:Promecispa voeltzkowi Weise 1909 by monotypy. Weise 1910d:442, 501 (faunal list), 1911a:53 (catalog), 1911b:80 (redescription); Uhmann 1931i:848 (museum list), 1958e:223 (catalog); Würmli 1975a:46 (genera); Seeno & Wilcox 1982:164 (catalog). Promecispa voeltzkowi Weise 1909 Promecispa voeltzkowi Weise 1909:112 (type:Madagascar, Kinkuni, ZMHB). Weise 1910d:442, 501 (faunal list), 1911a:53 (catalog), 1911b:80 (catalog); Uhmann 1931i:848 (type), 1958e:223 (catalog). Distribution. Madagascar. Food plant. Unknown. Promecotheca Blanchard 1853 Promecotheca Dejean 1837:387 Nomen Nudum. Guérin-Méneville 1840b:334 (note). Promecotheca Blanchard 1853:312. Type species:Hispa cyanipes Erichson 1834, designated by Baly 1858. -
Kilaka Forest
Kilaka Forest Conservation Area Management Plan Copyright: © 2016 Wildlife Conservation Society Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided that the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited withoutprior written consent of the copyright owner. Citation: WCS (2016) Kilaka Forest Conservation Area Management Plan. Wildlife Conservation Society, Suva, Fiji. 34 pp. Photograph (front cover): ©Ruci Lumelume/WCS Graphic design & Layout: cChange NOTE: This management plan may be amended from time to time. To obtain a copy of the current management plan, please contact: Wildlife Conservation Society Fiji Country Program 11 Ma’afu Street Suva Republic of Fiji Islands Telephone: +679 331 5174 Email: [email protected] Kilaka Forest Conservation Area Management Committee Kilaka Village Kubulau District Bua Province Republic of Fiji Kubulau Resource Management Committee Kubulau District Bua Province Republic of Fiji ENDORSEMENT On this day, 24 November, 2016 at Kilaka Village in the district of Kubulau, Bua Province, Vanua Levu in the Republic of Fiji Islands, we the undersigned endorse this management plan and its implementation. We urge the people of all communities in Kubulau and key stakeholders from government, private and non-government sectors to observe the plan and make every effort to ensure effective implementation. Minister, Ministry of Forests Tui -
Supplementary Material Local and Expert
10.1071/PC14920_AC CSIRO 2015 Pacific Conservation Biology 21 (3), 214-219 Supplementary material Local and expert knowledge improve conservation assessment of rare and iconic Fijian tree species Gunnar KeppelA,F, Alifereti NaikatiniB, Isaac A. RoundsC, Robert L. PresseyD, and Nunia T. ThomasE ASchool of Natural and Built Environments and Barbara Hardy Institute, University of South Australia, Mawson Lakes Campus, GPO Box 2471, Adelaide, SA 5001, Australia. BSouth Pacific Regional Herbarium, University of the South Pacific CConservation International, Suva, Fiji DAustralian Research Council Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, QLD 4811 Australia. ENatureFiji-MareqetiViti, 14 Hamilton-Beattie Street, Suva, Fiji FCorresponding author. Email: [email protected] Part 1: Overview of conservation status for each study species before this study. Acmopyle sahniana Buchholz & N.E. Gray (Podocarpaceae) is a rare conifer to 12 m tall, previously only reported from forested mountain ridges from central Viti Levu (Bush and Doyle 1997, Thomas 2013a). A detailed survey of the species recorded a total of 46 adult and 17 juvenile trees in 2 subpopulations (Bush 1997). A recent (2011) assessment reported another subpopulation near Fiji’s highest mountain, Mt. Tomanivi, and estimated the total size of that subpopulation at <100 mature individuals (Thomas 2013a). The species is listed as critically endangered (CR), based on small population size and low area of occupancy (<10 km2) (Thomas 2013a). Cynometra falcata A.Gray (Leguminosae) is reported as a slender tree to 4 m in height that until recently had only been known from two locations, one on Vanua Levu and another on Viti Levu (Smith 1985, WCMC 1998). -
Hydriastele Costata Click on Images to Enlarge
Species information Abo ut Reso urces Hom e A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Hydriastele costata Click on images to enlarge Family Arecaceae Scientific Name Hydriastele costata F.M.Bailey Bailey, F.M. (1898) Queensland Agricultural Journal 2(2): 129. Type: Somerset, Cape York Peninsula, Nov. 1897, Frank L. Jardine. Female flowers after flowering [not vouchered]. Copyright Common name J.L. Dowe Gulubia Palm Stem Solitary palm to 35 m tall, to 40 cm dbh, expanded at base; leaf scars to 35 mm wide; internodes to 25 cm long, smooth, grey. Leaves Usually 10-15 leaves, each to 4 m long, held out straight but lower ones tend to hang below horizontal; with 80-120 pinnae each side of rachis. Crownshaft to 150 cm long, light green suffused with lilac, with dense gray tomentum. Petiole 15-40 cm long; rachis to 350 cm long. Pinnae regularly arranged, to 127 cm long, Male and female flowers [not vouchered]. Copyright J.L. acuminate, pendulous. Dowe Flowers Inflorescence to 125 cm long, 40 cm wide. Flowers in threes, 1-2 male. Male flowers 10 mm in bud, not opening widely; sepals 1-1.5 mm x 1-1.5 mm, green; petals 9-10 mm x 3-5 mm, cream; stamens 6-24, 5-7 mm long; filaments 0.5 mm long; anthers 2-3 mm, bright yellow. Female flowers 1.5-3 x 2-3 mm in bud; sepals 0.2-0.5 x 0.5 mm, light green; petals 2-2.5 x 2-2.5 mm, cream-green; stigmas 0.2 mm long. -
A Floristic Study of Halmahera, Indonesia Focusing on Palms (Arecaceae) and Their Eeds Dispersal Melissa E
Florida International University FIU Digital Commons FIU Electronic Theses and Dissertations University Graduate School 5-24-2017 A Floristic Study of Halmahera, Indonesia Focusing on Palms (Arecaceae) and Their eedS Dispersal Melissa E. Abdo Florida International University, [email protected] DOI: 10.25148/etd.FIDC001976 Follow this and additional works at: https://digitalcommons.fiu.edu/etd Part of the Biodiversity Commons, Botany Commons, Environmental Studies Commons, and the Other Ecology and Evolutionary Biology Commons Recommended Citation Abdo, Melissa E., "A Floristic Study of Halmahera, Indonesia Focusing on Palms (Arecaceae) and Their eS ed Dispersal" (2017). FIU Electronic Theses and Dissertations. 3355. https://digitalcommons.fiu.edu/etd/3355 This work is brought to you for free and open access by the University Graduate School at FIU Digital Commons. It has been accepted for inclusion in FIU Electronic Theses and Dissertations by an authorized administrator of FIU Digital Commons. For more information, please contact [email protected]. FLORIDA INTERNATIONAL UNIVERSITY Miami, Florida A FLORISTIC STUDY OF HALMAHERA, INDONESIA FOCUSING ON PALMS (ARECACEAE) AND THEIR SEED DISPERSAL A dissertation submitted in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY in BIOLOGY by Melissa E. Abdo 2017 To: Dean Michael R. Heithaus College of Arts, Sciences and Education This dissertation, written by Melissa E. Abdo, and entitled A Floristic Study of Halmahera, Indonesia Focusing on Palms (Arecaceae) and Their Seed Dispersal, having been approved in respect to style and intellectual content, is referred to you for judgment. We have read this dissertation and recommend that it be approved. _______________________________________ Javier Francisco-Ortega _______________________________________ Joel Heinen _______________________________________ Suzanne Koptur _______________________________________ Scott Zona _______________________________________ Hong Liu, Major Professor Date of Defense: May 24, 2017 The dissertation of Melissa E. -
5 Pacific Ocean Region
Tropical Palms 107 5 PACIFIC OCEAN REGION This chapter considers the islands of the Pacific Ocean which are geographically divided into Micronesia, Melanesia and Polynesia. Micronesia delimits islands in the western Pacific and consists of the Mariana, Palau, Caroline, Marshall and Gilbert island groups. Melanesia lies to the northeast of Australia and includes New Caledonia, Vanuatu, Solomon Islands and Fiji. Polynesia designates the islands of the central Pacific, including Samoa (Western and American), French Polynesia (Marquesas, Society Islands, etc.) and Tonga. Papua New Guinea is also included within the scope of this chapter; politically the nation of Papua New Guinea consists of the eastern portion of the island of New Guinea and the Bismarck Archipelago as well as Bougainville. The following geographic areas where palms occur are excluded from discussion in this chapter and this report: The Hawaiian Islands; New Zealand, including the Kermadec Islands; Australia and its island territories (e.g. Lord Howe, Norfolk, Christmas and Cocos); and the Bonin and Ryukyu Islands belonging to Japan. The Pacific Ocean Region presents some very unusual patterns of native palm diversity. In the entire area of Micronesia there are only about ten species of native palms (Moore and Fosberg, 1956). The situation in Polynesia is comparable. In marked contrast Melanesia has much greater native palm diversity. For example, New Caledonia alone has 37 indigenous palm species, all endemic (Hodel and Pintaud, 1998; Moore and Uhl, 1984) and Vanuatu has 21 native palms (Dowe and Cabalion, 1996). Papua New Guinea and its islands hold a very rich diversity of palms, with about 270 native species in 31 genera (Baker and Dransfield, 2006; Essig, 1995; Hay, 1984). -
Report on the Endangered and Protected Species
STANDING COMMITTEE ON NATURAL RESOURCES REPORT ON THE ENDANGERED AND PROTECTED SPECIES (AMENDMENT) BILL (BILL NO. 6 OF 2016) PARLIAMENT OF THE REPUBLIC OF FIJI Parliamentary Paper No. 60 of 2016 Contents 1.0 Introduction…………………………………………………………………………………..3 2.0 Committee Remit and Member …………………………………………………….4 3.0 Analysis of the evidence received………………………………………………….5 4.0 Committee Conclusion ………………………………………………………………………………….5 5.0 Gender analysis…………………………………………………………………………….5-6 6.0 Committee Observation……………………………………………………………………………………………………...6 7.0 Amendments to the Bill……………………………………………………………...7-23 Amendment 1 ............................................................................................ 7 Annexe A – Glossary of terms used......................................................... 25 Annexe B – Oral evidence received .......................................................... 26 Annexe C – Written evidence received ................................................... 27 NATURAL RESOURCES COMMITTEE Page 2 | 27 Introduction The Natural Resources Committee was referred the Endangered and Protected Species (Amendment) Bill 2016 for second reading on 27thApril, 2016. The Committee has responsibility for examining the Bill and agreeing any appropriate amendments. The Endangered and Protected Species (Amendment) Bill 2016 amends the Endangered and Protected Species Act 2002 by adding more species for protection. The 2002 Act regulates the international trade, domestic trade, possession and transportation of species protected under the Convention on International Trade of Endangered Species and Wild Fauna and Flora (‘CITES’). To support the Committee in this process, it issued a call for written submissions on 7th May, 2016 and received two responses from a range of stakeholders. It held oral evidence sessions on 06th May, 2016 and 16th May, 2016 and heard from Department of Environment and the SODELPA Opposition Party Office. The Committee would like to extend its thanks to all those who participated and provided an essential contribution to this process. -
9 Costion Plant Endemism 133-166 PROOFS
Micronesica 41(1): 131–164, 2009 Plant Endemism, Rarity, and Threat in Palau, Micronesia: A Geographical Checklist and Preliminary Red List Assessment 1 CRAIG M. COSTION Department of Ecology and Evolutionary Biology, School of Earth and Environmental Sciences, University of Adelaide, Adelaide SA 5001 [email protected] ANN HILLMANN KITALONG The Environment, Inc., P.O. Box 1696, Koror, Palau 96940 TARITA HOLM Palau Conservation Society/PALARIS, P.O. Box 1811, Koror, Palau, 96940 Abstract—An official checklist of the endemic plant species of Palau has been long awaited, and is presented here for the first time. For each species a substrate limitation, growth form, and relative abundance is listed. In addition an IUCN red list assessment was conducted using all available data. For over half of the endemic species there is insufficient data to provide a red listing status however an expected minimum number of threatened plants out of the total is inferred. Approximately 15% of Palau’s endemic plants are believed to be only known from the type collection and many more only known from a few collections. These taxa however may now be prioritized and targeted for future inventory and research. The taxonomic robustness of several of these taxa is questionable and it is expected that more endemic species will be lost to synonymy in the future. Previous estimations have significantly over-estimated the rate of plant endemism in Palau (e.g., 194). Here, 130 plants are recognized for Palau, making its level of plant endem- ism comparable to some of its neighboring Micronesian islands to the east, notably Guam and Pohnpei. -
Obdiplostemony: the Occurrence of a Transitional Stage Linking Robust Flower Configurations
Annals of Botany 117: 709–724, 2016 doi:10.1093/aob/mcw017, available online at www.aob.oxfordjournals.org VIEWPOINT: PART OF A SPECIAL ISSUE ON DEVELOPMENTAL ROBUSTNESS AND SPECIES DIVERSITY Obdiplostemony: the occurrence of a transitional stage linking robust flower configurations Louis Ronse De Craene1* and Kester Bull-Herenu~ 2,3,4 1Royal Botanic Garden Edinburgh, Edinburgh, UK, 2Departamento de Ecologıa, Pontificia Universidad Catolica de Chile, 3 4 Santiago, Chile, Escuela de Pedagogıa en Biologıa y Ciencias, Universidad Central de Chile and Fundacion Flores, Ministro Downloaded from https://academic.oup.com/aob/article/117/5/709/1742492 by guest on 24 December 2020 Carvajal 30, Santiago, Chile * For correspondence. E-mail [email protected] Received: 17 July 2015 Returned for revision: 1 September 2015 Accepted: 23 December 2015 Published electronically: 24 March 2016 Background and Aims Obdiplostemony has long been a controversial condition as it diverges from diploste- mony found among most core eudicot orders by the more external insertion of the alternisepalous stamens. In this paper we review the definition and occurrence of obdiplostemony, and analyse how the condition has impacted on floral diversification and species evolution. Key Results Obdiplostemony represents an amalgamation of at least five different floral developmental pathways, all of them leading to the external positioning of the alternisepalous stamen whorl within a two-whorled androe- cium. In secondary obdiplostemony the antesepalous stamens arise before the alternisepalous stamens. The position of alternisepalous stamens at maturity is more external due to subtle shifts of stamens linked to a weakening of the alternisepalous sector including stamen and petal (type I), alternisepalous stamens arising de facto externally of antesepalous stamens (type II) or alternisepalous stamens shifting outside due to the sterilization of antesepalous sta- mens (type III: Sapotaceae). -
Florida Plant Immigrants
- •'' '.. n FLORIDA PLANT IMMIGRANTS OCCASIONAL PAPER No. 7 FAIRCHILD TROPICAL GARDEN THE RIB-SEED PALMS IN FLORIDA THE LADY PALMS L. H. BAILEY COCONUT GROVE, FLORIDA No. 7 • JANUARY 1, 1940 THE RIB-SEED PALMS IN FLORIDA FEW EXOTIC small palms with bright red makes a handsome and clean addition to the A little fruits and deeply ribbed seeds are home property. more or less planted in southern Florida, but they This palm and its associates are tender to are so similar to each frost, but as they are other and the names of usually grown near them are so confused buildings or under the that we may now try to protection of large understand them. They trees they are not often are seldom mentioned injured. They come in common writings readily from seeds and on palms, at least not grow rapidly into under their proper comely subjects. They names. have good shape and The picture on this color even when young. page identifies the How far north they may commonest one of the stand in the open I do rib-seeds. It is seen fre- not know. If we can quently from Palm bring them more ac- Beach southward about tively to the attention buildings, in yards, of observers we may along driveways, and it soon accumulate many should make a good records of their distri- tub subj ect for verandas bution in Florida. I in its juvenile state. have not noted them in This tree I have other parts of the called the Solitaire United States, but they palm to distinguish it are frequently planted from the Cluster palms in the tropics. -
Value Island Biodiversity It’S Our Life!
VALUE ISLAND BIODivERSITY It’s Our Life! Secretariat of the Pacific Regional Environment Programme 1 CONTENTS Introduction Introduction David Sheppard, Director SPREP 3 VALUE ISLAND BIODIVERSITY Campaign Launch Kosi Latu, Deputy Director SPREP 5 It’s Our Life! Pacific getting ready to meet new targets 6 Emerald of the Isles 7 David Sheppard, Director, SPREP Rare giant box crab 7 he Pacific islands region swung into action The hive of activity across the region culmi- Micronesia’s Go Local 9 T with determination to observe 2010 as the nated at the 10th Conference of Parties to the Convention on Biological Diversity (CBD International Year of Biodiversity (IYOB). COP10) in Nagoya, Japan. The region’s COP10 Climate Change and Invasive Species 10 communication strategy, The Pacific Voyage, The Biodiversity Bus 11 In 2009 following discussions with participants a flower, was used to convey the over-arch- highlighted the unique biodiversity of the Pa- at the Nature Conservation Roundtable held in ing message that we are all intertwined with cific islands and showcased our PYOB activities Pacific Ocean for your Children 12 Solomon Islands, a draft framework for imple- nature. to the world. The Pacific Voyage also served to menting the International Year of Biodiversity enable the Pacific islands to be heard during The slogan, Value Island Biodiversity – it’s our life, (IYOB) in the Pacific was circulated regionally negotiations and discussions as one voice. And Island Wear Biodiversity and Fashion 13 resounded well with many of SPREP’s Pacific for comment and input. Member countries and we were successful! Issues of importance to island members and was used extensively in territories then endorsed the framework at the the region – invasive species, climate change, Polynesia, Micronesia Challenged 18 correspondence and other publications, and 20th SPREP Meeting held in Apia in 2009 and coastal and marine biodiversity and financing on stickers and posters.