Endangered and Protected Species Act 2002
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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 -
Studies on New Guinea Moths. 1. Introduction (Lepidoptera)
PROC. ENTOMOL. SOC. WASH. 105(4), 2003, pp. 1034-1042 STUDIES ON NEW GUINEA MOTHS. 1. INTRODUCTION (LEPIDOPTERA) SCOTT E. MILLER, VOJTECH NOVOTNY, AND YVES BASSET (SEM) Department of Systematic Biology, National Museum of Natural History, Smith- sonian Institution, Washington, DC 20560-0105, U.S.A. (e-mail: [email protected]. edu); (VN) Institute of Entomology, Czech Academy of Sciences and Biological Faculty, University of South Bohemia, Branisovska 31, 370 05 Ceske Budejovice, Czech Republic; (YB) Smithsonian Tropical Research Institute, Apartado 2072, Balboa, Ancon, Panama Abstract.•This is the first in a series of papers providing taxonomic data in support of ecological and biogeographic studies of moths in New Guinea. The primary study is an extensive inventory of the caterpillar fauna of a lowland rainforest site near Madang, Papua New Guinea, from 1994•2001. The inventory focused on the Lepidoptera com- munity on 71 woody plant species representing 45 genera and 23 families. During the study, 46,457 caterpillars representing 585 species were sampled, with 19,660 caterpillars representing 441 species reared to adults. This introductory contribution is intended to provide background on the project, including descriptions of the study site, sampling methods, and taxonomic methods. Key Words: Malesia, Papua New Guinea, Lepidoptera, biodiversity, rearing, community ecology A very large portion of tropical biodi- 1992 and 1993 (Basset 1996, Basset et al. versity consists of herbivorous insects, and 1996). This paper represents the first in a among them, Lepidoptera are among the series of papers providing taxonomic doc- most amenable to study. To better under- umentation in support of the broader stud- stand the structure and maintenance of trop- ies, and is intended to provide general back- ical biodiversity, we undertook a series of ground, including descriptions of the study related inventories of Lepidoptera in New site, sampling methods, and taxonomic Guinea. -
DNA Barcoding Confirms Polyphagy in a Generalist Moth, Homona Mermerodes (Lepidoptera: Tortricidae)
Molecular Ecology Notes (2007) 7, 549–557 doi: 10.1111/j.1471-8286.2007.01786.x BARCODINGBlackwell Publishing Ltd DNA barcoding confirms polyphagy in a generalist moth, Homona mermerodes (Lepidoptera: Tortricidae) JIRI HULCR,* SCOTT E. MILLER,† GREGORY P. SETLIFF,‡ KAROLYN DARROW,† NATHANIEL D. MUELLER,§ PAUL D. N. HEBERT¶ and GEORGE D. WEIBLEN** *Department of Entomology, Michigan State University, 243 Natural Sciences Building, East Lansing, Michigan 48824, USA, †National Museum of Natural History, Smithsonian Institution, Box 37012, Washington, DC 20013-7012, USA, ‡Department of Entomology, University of Minnesota, 1980 Folwell Avenue, Saint Paul, Minnesota 55108–1095 USA, §Saint Olaf College, 1500 Saint Olaf Avenue, Northfield, MN 55057, USA,¶Department of Integrative Biology, University of Guelph, Guelph, Ontario, Canada N1G2W1, **Bell Museum of Natural History and Department of Plant Biology, University of Minnesota, 220 Biological Sciences Center, 1445 Gortner Avenue, Saint Paul, Minnesota 55108–1095, USA Abstract Recent DNA barcoding of generalist insect herbivores has revealed complexes of cryptic species within named species. We evaluated the species concept for a common generalist moth occurring in New Guinea and Australia, Homona mermerodes, in light of host plant records and mitochondrial cytochrome c oxidase I haplotype diversity. Genetic divergence among H. mermerodes moths feeding on different host tree species was much lower than among several Homona species. Genetic divergence between haplotypes from New Guinea and Australia was also less than interspecific divergence. Whereas molecular species identification methods may reveal cryptic species in some generalist herbivores, these same methods may confirm polyphagy when identical haplotypes are reared from multiple host plant families. A lectotype for the species is designated, and a summarized bibliography and illustrations including male genitalia are provided for the first time. -
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). -
Republic of Fiji: the State of the World's Forest Genetic Resources
REPUBLIC OF FIJI This country report is prepared as a contribution to the FAO publication, The Report on the State of the World’s Forest Genetic Resources. The content and the structure are in accordance with the recommendations and guidelines given by FAO in the document Guidelines for Preparation of Country Reports for the State of the World’s Forest Genetic Resources (2010). These guidelines set out recommendations for the objective, scope and structure of the country reports. Countries were requested to consider the current state of knowledge of forest genetic diversity, including: Between and within species diversity List of priority species; their roles and values and importance List of threatened/endangered species Threats, opportunities and challenges for the conservation, use and development of forest genetic resources These reports were submitted to FAO as official government documents. The report is presented on www. fao.org/documents as supportive and contextual information to be used in conjunction with other documentation on world forest genetic resources. The content and the views expressed in this report are the responsibility of the entity submitting the report to FAO. FAO may not be held responsible for the use which may be made of the information contained in this report. STATE OF THE FOREST GENETIC RESOURCES IN FIJI Department of Forests Ministry of Fisheries and Forests for The Republic of Fiji Islands and the Secreatriat of Pacific Communities (SPC) State of the Forest Genetic Resources in Fiji _____________________________________________________________________________________________________________________ Table of Contents Executve Summary ………………………………………………………………………………………………………………………..…….. 5 Introduction ………………………………………………………………………………………………………………………………..…….. 6 Chapter 1: The Current State of the Forest Genetic Resources in Fiji ………………………………………………………………….……. -
Floristic Relationships of New Caledonian Rainforest Phanerogams
Extract from Telopea 2(6): 631-679 (1986) 63 1 FLORISTIC RELATIONSHIPS OF NEW CALEDONIAN RAINFOREST PHANEROGAMS PH.MORAT!, J.-M. VELLONI& H. S. MACKEE~ (Accepted for publication 16.9.1983) ABSTRACT Morat, Ph.’, Veìllon, J.-M.’ & MacKee, H. S.2 (‘Centre ORSTOM, B.P. A5 Cedex, Nouméa, New Caledonia; 2L3.P. 3349, Nouméa, New Caledonia) 1984. Floristic relatiomhips of New Caledonian rainforest phanerogams. Telopea 2[4): 631-679 - A detailed analysis of the New Caledonian rainforest flora is given; 1499 species in 365 genera and 108 families are listed. Distribution of the species within New Caledonia is given in terms of specificity to rainforest (forestInon-forest and forest occurrence) and to substrate (only ultrabasiclabsent from ultrabasic/present on ultrabasic and other substr: :ss). Distribution of genera is presented according’to occurrences in 12 phyto- geographic units from endemic to pantropical. Sources of information are given. Comparisons with the whole New Caledonian phanerogamic flora are made; 46% of genera and species and 66% of families occur in the rainforest. For the flora the level of specific endemism is c. 75%. Floristic affinities are assessed by: comparison of numbers of genera shared with other regions (pantropical genera included/excluded); and numbers of genera shared exclusively by New Caledonia and 2, 3, 4, 5 or 6 other regions. In these comparisons Australia, New Guinea, Malesia, Fiji, the New Hebrides, the Solomon Islands and then New Zealand have the most genera in common with New Caledonia. A floristic affinity Co-efficient for each territory was calculated from the proportion of the number of common genera to the number of territories in which they occur, for groups of two to six territories. -
Summary Report on Forests of the Mataqali Nadicake Kilaka, Kubulau District, Bua, Vanua Levu
SUMMARY REPORT ON FORESTS OF THE MATAQALI NADICAKE KILAKA, KUBULAU DISTRICT, BUA, VANUA LEVU By Gunnar Keppel (Biology Department, University of the South Pacific) INTRODUCTION I was approached by Dr. David Olson of the Wildlife Conservation Society (WCS) to assess the type, status and quality of the forest in Kubulau District, Bua, Vanua Levu. I initially spent 2 days, Friday (28/10/2005) afternoon and the whole of Saturday (29/10/2005), in Kubulau district. This invitation was the result of interest by some landowning family clans (mataqali) to protect part of their land and the offer by WCS to assist in reserving part of their land for conservation purposes. On Friday I visited two forest patches (one logged about 40 years ago and another old-growth) near the coast and Saturday walking through the forests in the center of the district. Because of the scarcity of data obtained (and because the forest appeared suitable for my PhD research), I decided to return to the district for a more detailed survey of the northernmost forests of Kubulau district from Saturday (12/11/2005) to Tuesday (22/11/2005). Upon returning, I found out that the mataqali Nadicake Nadi had abandoned plans to set up a reserve and initiated steps to log their forests. Therefore, I decided to focus my research on the land of the mataqali Nadicake Kilaka only. My objectives were the following: 1) to determine the types of vegetation present 2) to produce a checklist of the flora and, through this list, identify rare and threatened species in the reserve 3) to undertake a quantitative survey of the northernmost forests (lowland tropical rain forest) by setting up 4 permanent 50 ×50m plots 4) to assess the status of the forests 5) to determine the state and suitability of the proposed reserve 6) to assess possible threats to the proposed reserve. -
Chapter One 1.0 Introduction and Background to The
CHAPTER ONE 1.0 INTRODUCTION AND BACKGROUND TO THE STUDY Loganiaceae is a family of flowering plants classified in the Order Gentianales (Bendre, 1975). The family was first suggested by Robert Brown in 1814 and validly published by von Martius in 1827 (Nicholas and Baijnath, 1994). Members habits are in form of trees, shrubs, woody climbers and herbs. Some are epiphytes while some members are furnished with spines or tendrils (Bendre, 1975). They are distributed mainly in the tropics, subtropics and a few in temperate regions (Backlund et al., 2000). Earlier treatments of the family have included up to 30 genera, 600 species (Leeuwenberg and Leenhouts, 1980; Mabberley, 1997) but were later reduced to 400 species in 15 genera, with some species extending into temperate Australia and North America (Struwe et al., 1994; Dunlop, 1996; Backlund and Bremer, 1998). Morphological studies have demonstrated that this broadly defined Loganiaceae was a polyphyletic assemblage and numerous genera have been removed from it to other families (sometimes to other Orders), e.g. Gentianaceae, Gelsemiaceae, Plocospermataceae, Tetrachondraceae, Buddlejaceae, and Gesneriaceae (Backlund and Bremer, 1998; Backlund et al., 2000). The family has undergone numerous revisions that have expanded and contracted its circumscription, ranging from one genus at its smallest (Takhtajan, 1997; Smith et al., 1997) to 30 at its largest (Leeuwenberg and Leenhouts, 1980). One of the current infrafamilial classifications contains four tribes: Antonieae Endl., Loganieae Endl., Spigelieae Dum. (monotypic), and Strychneae Dum. (Struwe et al., 1994). The tribes Loganieae and Antonieae are supported by molecular data, but Strychneae is not (Backlund et al., 2000). -
Types of Vegetation Occuring on Santo
in BOUCHET P., LE GUYADER H. & PASCAL O. (Eds), The Natural History of Santo. MNHN, Paris; IRD, Marseille; PNI, Paris. 572 p. (Patrimoines naturels; 70). Types of Vegetation Occurring on Santo Jérôme Munzinger, Porter P. Lowry II & Jean-Noël Labat The Santo 2006 expedition was Table 5: Vegetation types in Vanuatu proposed by Mueller- designed to carry out detailed explo- Dombois and Fosberg. ration of the botanical diversity 1. Lowland rain forest present on the island. A wide diver- sity of vegetation types were there- a. High-stature forests on old volcanic ash fore studied, covering the full range b. Medium-stature forest heavily covered with lianas extending from what can be regarded c. Complex forest scrub densely covered with lianas as "extremes" on a scale from natu- d. Alluvial and floodplain forests ral, nearly undisturbed areas to those e. Agathis-Calophyllum forest that have been profoundly modified f. Mixed-species forests without gymnosperms and by man. Large areas have been trans- Calophyllum formed by humans — partially or completely — through clearing, fire, 2. Montane cloud forest and related vegetation Principal and other means, in an effort to meet basic needs for food, shelter, fiber, 3. Seasonal forest, scrub and grassland grazing land for livestock, etc., although such a. Semi-deciduous transitions forests habitats exist only because they are created and b. Acacia spirorbis forest maintained by man or by domesticated animals. c. Leucaena thicket, savanna and grassland At the other extreme, Santo’s vegetation includes nearly pristine formations that result from the 4. Vegetation on new volcanic surfaces natural processes of evolution and succession and are self-maintaining, provided they are not subject 5. -
Explosive Radiation of Malpighiales Supports a Mid-Cretaceous Origin of Modern Tropical Rain Forests
Explosive Radiation of Malpighiales Supports a Mid-Cretaceous Origin of Modern Tropical Rain Forests The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Davis, Charles C., Campbell O. Webb, Kenneth J. Wurdack, Carlos A. Jaramillo, and Michael J. Donoghue. 2005. Explosive radiation of Malpighiales supports a mid-Cretaceous origin of modern tropical rain forests. American Naturalist 165(3): E36-E65. Published Version http://dx.doi.org/10.1086/428296 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:2710469 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA vol. 165, no. 3 the american naturalist march 2005 E-Article Explosive Radiation of Malpighiales Supports a Mid-Cretaceous Origin of Modern Tropical Rain Forests Charles C. Davis,1,* Campbell O. Webb,2,† Kenneth J. Wurdack,3,‡ Carlos A. Jaramillo,4,§ and Michael J. Donoghue2,k 1. Department of Ecology and Evolutionary Biology, University of Keywords: biome evolution, fossils, K/T boundary, Malpighiales, pe- Michigan Herbarium, Ann Arbor, Michigan 48108-2287; nalized likelihood, tropical rain forest. 2. Department of Ecology and Evolutionary Biology, Yale University, P.O. Box 208106, New Haven, Connecticut 06520; 3. Department of Botany and Laboratories of Analytical Biology, Modern tropical rain forests are one of the most important Smithsonian Institution, P.O. Box 37012, National Museum of and species rich biomes on the planet. -
Cunoniaceae.Pdf
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 Cunoniaceae Family Profile Cunoniaceae Family Description A family of about 27 genera and 280 species, mostly in the southern hemisphere, in South America north to Mexico and the West Indies, Malesia, Australia, New Caledonia and the SW Pacific islands; 14 genera occur naturally in Australia. Genera Ackama - A genus of 4 species in Australia and New Zealand; two species occur naturally in Australia. Hoogland (1979); Heslewood & Wilson (2013). Ceratopetalum - A genus of about eight species restricted to New Guinea and Australia; nine species occur naturally in Australia. Hoogland (1960, 1982). Davidsonia - A genus of one or two species endemic to Australia. Cronquist (1981); Floyd (1989). Eucryphia - A genus of about seven species in Australia and Chile; five species occur naturally in Australia. Forster & Hyland (1997); Taylor & Hill (1996). Gillbeea - A genus of three species in New Guinea and Australia; two species occurs naturally in Australia. Rozefelds & Pellow (2000). Karrabina - A genus of two species endemic to Australia. Hutchinson (1967); Schimanski & Rozefelds (2002); Hopkins et al (2013). Pseudoweinmannia - A monotypic genus endemic to Australia. Francis (1970). Pullea - A genus of three species in New Guinea, Australia and Fiji; one species occurs naturally in Australia. Hoogland (1979). Schizomeria - A genus of about 18 species in the Moluccas, New Guinea and Australia; two species occur naturally in Australia. Francis (1970). Spiraeanthemum - A genus of 20 species in the Molluccas, New Guinea and the Solomon Islands, Australia, New Caledonia and Fiji; one species occurs naturally in Australia.