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Growing Plants for Hawaiian Lei ‘A‘Ali‘I
6 Growing Plants for Hawaiian Lei ‘a‘ali‘i OTHER COMMON NAMES: ‘a‘ali‘i kū range of habitats from dunes at sea makani, ‘a‘ali‘i kū ma kua, kū- level up through leeward and dry makani, hop bush, hopseed bush forests and to the highest peaks SCIENTIFIC NAME: Dodonaea viscosa CURRENT STATUS IN THE WILD IN HAWAI‘I: common FAMILY: Sapindaceae (soapberry family) CULTIVARS: female cultivars such as ‘Purpurea’ and ‘Saratoga’ have NATURAL SETTING/LOCATION: indigenous, been selected for good fruit color pantropical species, found on all the main Hawaiian Islands except Kaho‘olawe; grows in a wide Growing your own PROPAGATION FORM: seeds; semi-hardwood cuttings or air layering for selected color forms PREPLANTING TREATMENT: step on seed capsule to release small, round, black seeds, or use heavy gloves and rub capsules vigorously between hands; put seeds in water that has been brought to a boil and removed from heat, soak for about 24 hours; if seeds start to swell, sow imme- diately; discard floating, nonviable seeds; use strong rooting hormone on cuttings TEMPERATURE: PLANTING DEPTH: sow seeds ¼" deep in tolerates dry heat; tem- after fruiting period to shape or keep medium; insert base of cutting 1–2" perature 32–90°F short; can be shaped into a small tree or maintained as a shrub, hedge, or into medium ELEVATION: 10–7700' espalier (on a trellis) GERMINATION TIME: 2–4 weeks SALT TOLERANCE: good (moderate at SPECIAL CULTURAL HINTS: male and female CUTTING ROOTING TIME: 1½–3 months higher elevations) plants are separate, although bisex- WIND RESISTANCE: -
Pu'u Wa'awa'a Biological Assessment
PU‘U WA‘AWA‘A BIOLOGICAL ASSESSMENT PU‘U WA‘AWA‘A, NORTH KONA, HAWAII Prepared by: Jon G. Giffin Forestry & Wildlife Manager August 2003 STATE OF HAWAII DEPARTMENT OF LAND AND NATURAL RESOURCES DIVISION OF FORESTRY AND WILDLIFE TABLE OF CONTENTS TITLE PAGE ................................................................................................................................. i TABLE OF CONTENTS ............................................................................................................. ii GENERAL SETTING...................................................................................................................1 Introduction..........................................................................................................................1 Land Use Practices...............................................................................................................1 Geology..................................................................................................................................3 Lava Flows............................................................................................................................5 Lava Tubes ...........................................................................................................................5 Cinder Cones ........................................................................................................................7 Soils .......................................................................................................................................9 -
Rhinogobius Mizunoi, a New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Bull. Kanagawa prefect. Mus. (Nat. Sci.), no. 46, pp. 79-95, Feb. 2017 79 Original Article Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan Toshiyuki Suzuki 1), Koichi Shibukawa 2) & Masahiro Aizawa 3) Abstract. A new freshwater goby, Rhinogobius mizunoi, is described based on six specimens from a freshwater stream in Shizuoka Prefecture, Japan. The species is distinguished from all congeneric species by the following combination of characters: I, 8 second dorsal-fin rays; 18–20 pectoral-fin rays; 13–18 predorsal scales; 33–35 longitudinal scales; 8 or 9 transverse scales; 10+16=26 vertebrae 26; first dorsal fin elongate in male, its distal tip reaching to base of fourth branched ray of second dorsal fin in males when adpressed; when alive or freshly-collected, cheek with several pale sky spots; caudal fin without distinct rows of dark dots; a pair of vertically- arranged dark brown blotches at caudal-fin base in young and females. Key words: amphidoromous, fish taxonomy, Rhinogobius sp. CO, valid species Introduction 6–11 segmented rays; anal fin with a single spine and 5–11 The freshwater gobies of the genus Rhinogobius Gill, segmented rays; pectoral fin with 14–23 segmented rays; 1859 are widely distributed in the East and Southeast pelvic fin with a single spine and five segmented rays; Asian regions, including the Russia Far East, Japan, 25–44 longitudinal scales; 7–16 transverse scales; P-V 3/ Korea, China, Taiwan, the Philippines, Vietnam, Laos, II II I I 0/9; 10–11+15–18= 25–29 vertebrae; body mostly Cambodia, and Thailand (Chen & Miller, 2014). -
Checklist of Fish and Invertebrates Listed in the CITES Appendices
JOINTS NATURE \=^ CONSERVATION COMMITTEE Checklist of fish and mvertebrates Usted in the CITES appendices JNCC REPORT (SSN0963-«OStl JOINT NATURE CONSERVATION COMMITTEE Report distribution Report Number: No. 238 Contract Number/JNCC project number: F7 1-12-332 Date received: 9 June 1995 Report tide: Checklist of fish and invertebrates listed in the CITES appendices Contract tide: Revised Checklists of CITES species database Contractor: World Conservation Monitoring Centre 219 Huntingdon Road, Cambridge, CB3 ODL Comments: A further fish and invertebrate edition in the Checklist series begun by NCC in 1979, revised and brought up to date with current CITES listings Restrictions: Distribution: JNCC report collection 2 copies Nature Conservancy Council for England, HQ, Library 1 copy Scottish Natural Heritage, HQ, Library 1 copy Countryside Council for Wales, HQ, Library 1 copy A T Smail, Copyright Libraries Agent, 100 Euston Road, London, NWl 2HQ 5 copies British Library, Legal Deposit Office, Boston Spa, Wetherby, West Yorkshire, LS23 7BQ 1 copy Chadwick-Healey Ltd, Cambridge Place, Cambridge, CB2 INR 1 copy BIOSIS UK, Garforth House, 54 Michlegate, York, YOl ILF 1 copy CITES Management and Scientific Authorities of EC Member States total 30 copies CITES Authorities, UK Dependencies total 13 copies CITES Secretariat 5 copies CITES Animals Committee chairman 1 copy European Commission DG Xl/D/2 1 copy World Conservation Monitoring Centre 20 copies TRAFFIC International 5 copies Animal Quarantine Station, Heathrow 1 copy Department of the Environment (GWD) 5 copies Foreign & Commonwealth Office (ESED) 1 copy HM Customs & Excise 3 copies M Bradley Taylor (ACPO) 1 copy ^\(\\ Joint Nature Conservation Committee Report No. -
Taxonomic Checklist of CITES Listed Coral Species Part II
CoP16 Doc. 43.1 (Rev. 1) Annex 5.2 (English only / Únicamente en inglés / Seulement en anglais) Taxonomic Checklist of CITES listed Coral Species Part II CORAL SPECIES AND SYNONYMS CURRENTLY RECOGNIZED IN THE UNEP‐WCMC DATABASE 1. Scleractinia families Family Name Accepted Name Species Author Nomenclature Reference Synonyms ACROPORIDAE Acropora abrolhosensis Veron, 1985 Veron (2000) Madrepora crassa Milne Edwards & Haime, 1860; ACROPORIDAE Acropora abrotanoides (Lamarck, 1816) Veron (2000) Madrepora abrotanoides Lamarck, 1816; Acropora mangarevensis Vaughan, 1906 ACROPORIDAE Acropora aculeus (Dana, 1846) Veron (2000) Madrepora aculeus Dana, 1846 Madrepora acuminata Verrill, 1864; Madrepora diffusa ACROPORIDAE Acropora acuminata (Verrill, 1864) Veron (2000) Verrill, 1864; Acropora diffusa (Verrill, 1864); Madrepora nigra Brook, 1892 ACROPORIDAE Acropora akajimensis Veron, 1990 Veron (2000) Madrepora coronata Brook, 1892; Madrepora ACROPORIDAE Acropora anthocercis (Brook, 1893) Veron (2000) anthocercis Brook, 1893 ACROPORIDAE Acropora arabensis Hodgson & Carpenter, 1995 Veron (2000) Madrepora aspera Dana, 1846; Acropora cribripora (Dana, 1846); Madrepora cribripora Dana, 1846; Acropora manni (Quelch, 1886); Madrepora manni ACROPORIDAE Acropora aspera (Dana, 1846) Veron (2000) Quelch, 1886; Acropora hebes (Dana, 1846); Madrepora hebes Dana, 1846; Acropora yaeyamaensis Eguchi & Shirai, 1977 ACROPORIDAE Acropora austera (Dana, 1846) Veron (2000) Madrepora austera Dana, 1846 ACROPORIDAE Acropora awi Wallace & Wolstenholme, 1998 Veron (2000) ACROPORIDAE Acropora azurea Veron & Wallace, 1984 Veron (2000) ACROPORIDAE Acropora batunai Wallace, 1997 Veron (2000) ACROPORIDAE Acropora bifurcata Nemenzo, 1971 Veron (2000) ACROPORIDAE Acropora branchi Riegl, 1995 Veron (2000) Madrepora brueggemanni Brook, 1891; Isopora ACROPORIDAE Acropora brueggemanni (Brook, 1891) Veron (2000) brueggemanni (Brook, 1891) ACROPORIDAE Acropora bushyensis Veron & Wallace, 1984 Veron (2000) Acropora fasciculare Latypov, 1992 ACROPORIDAE Acropora cardenae Wells, 1985 Veron (2000) CoP16 Doc. -
Trait Decoupling Promotes Evolutionary Diversification of The
Trait decoupling promotes evolutionary diversification of the trophic and acoustic system of damselfishes rspb.royalsocietypublishing.org Bruno Fre´de´rich1, Damien Olivier1, Glenn Litsios2,3, Michael E. Alfaro4 and Eric Parmentier1 1Laboratoire de Morphologie Fonctionnelle et Evolutive, Applied and Fundamental Fish Research Center, Universite´ de Lie`ge, 4000 Lie`ge, Belgium 2Department of Ecology and Evolution, University of Lausanne, 1015 Lausanne, Switzerland Research 3Swiss Institute of Bioinformatics, Ge´nopode, Quartier Sorge, 1015 Lausanne, Switzerland 4Department of Ecology and Evolutionary Biology, University of California, Los Angeles, CA 90095, USA Cite this article: Fre´de´rich B, Olivier D, Litsios G, Alfaro ME, Parmentier E. 2014 Trait decou- Trait decoupling, wherein evolutionary release of constraints permits special- pling promotes evolutionary diversification of ization of formerly integrated structures, represents a major conceptual the trophic and acoustic system of damsel- framework for interpreting patterns of organismal diversity. However, few fishes. Proc. R. Soc. B 281: 20141047. empirical tests of this hypothesis exist. A central prediction, that the tempo of morphological evolution and ecological diversification should increase http://dx.doi.org/10.1098/rspb.2014.1047 following decoupling events, remains inadequately tested. In damselfishes (Pomacentridae), a ceratomandibular ligament links the hyoid bar and lower jaws, coupling two main morphofunctional units directly involved in both feeding and sound production. Here, we test the decoupling hypothesis Received: 2 May 2014 by examining the evolutionary consequences of the loss of the ceratomandib- Accepted: 9 June 2014 ular ligament in multiple damselfish lineages. As predicted, we find that rates of morphological evolution of trophic structures increased following the loss of the ligament. -
Scleractinian Reef Corals: Identification Notes
SCLERACTINIAN REEF CORALS: IDENTIFICATION NOTES By JACKIE WOLSTENHOLME James Cook University AUGUST 2004 DOI: 10.13140/RG.2.2.24656.51205 http://dx.doi.org/10.13140/RG.2.2.24656.51205 Scleractinian Reef Corals: Identification Notes by Jackie Wolstenholme is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. TABLE OF CONTENTS TABLE OF CONTENTS ........................................................................................................................................ i INTRODUCTION .................................................................................................................................................. 1 ABBREVIATIONS AND DEFINITIONS ............................................................................................................. 2 FAMILY ACROPORIDAE.................................................................................................................................... 3 Montipora ........................................................................................................................................................... 3 Massive/thick plates/encrusting & tuberculae/papillae ................................................................................... 3 Montipora monasteriata .............................................................................................................................. 3 Massive/thick plates/encrusting & papillae ................................................................................................... -
Reef Fishes of the Bird's Head Peninsula, West
Check List 5(3): 587–628, 2009. ISSN: 1809-127X LISTS OF SPECIES Reef fishes of the Bird’s Head Peninsula, West Papua, Indonesia Gerald R. Allen 1 Mark V. Erdmann 2 1 Department of Aquatic Zoology, Western Australian Museum. Locked Bag 49, Welshpool DC, Perth, Western Australia 6986. E-mail: [email protected] 2 Conservation International Indonesia Marine Program. Jl. Dr. Muwardi No. 17, Renon, Denpasar 80235 Indonesia. Abstract A checklist of shallow (to 60 m depth) reef fishes is provided for the Bird’s Head Peninsula region of West Papua, Indonesia. The area, which occupies the extreme western end of New Guinea, contains the world’s most diverse assemblage of coral reef fishes. The current checklist, which includes both historical records and recent survey results, includes 1,511 species in 451 genera and 111 families. Respective species totals for the three main coral reef areas – Raja Ampat Islands, Fakfak-Kaimana coast, and Cenderawasih Bay – are 1320, 995, and 877. In addition to its extraordinary species diversity, the region exhibits a remarkable level of endemism considering its relatively small area. A total of 26 species in 14 families are currently considered to be confined to the region. Introduction and finally a complex geologic past highlighted The region consisting of eastern Indonesia, East by shifting island arcs, oceanic plate collisions, Timor, Sabah, Philippines, Papua New Guinea, and widely fluctuating sea levels (Polhemus and the Solomon Islands is the global centre of 2007). reef fish diversity (Allen 2008). Approximately 2,460 species or 60 percent of the entire reef fish The Bird’s Head Peninsula and surrounding fauna of the Indo-West Pacific inhabits this waters has attracted the attention of naturalists and region, which is commonly referred to as the scientists ever since it was first visited by Coral Triangle (CT). -
Plants of Cat Tien National Park DANH LỤC THỰC VẬT VƯỜN
Plants of Cat Tien National Park 22 January 2017 * DANH LỤC THỰC VẬT VƯỜN QUỐC GIA CÁT TIÊN Higher Family Chi - Loài NGÀNH / LỚP v.v. HỌ / HỌ PHỤ Rec. No. Clas. (& sub~) Species Authority ssp., var., syn. etc. & notes TÊN VIỆT NAM Ds Cd Mã số Clade: Embryophyta Nhánh: Thực vật có phôi (Division) Marchantiophyta Liverworts Ngành Rêu tản (Division) Anthocerotophyta Hornworts Ngành Rêu sừng (Division) Bryophyta Mosses Ngành Rêu Tracheophyta: Vascular plants: Thực vật có mạch: (Division) Lycopodiophyta clubmosses, etc Ngành Thạch tùng Lycopodiaceae 1. HỌ THẠCH TÙNG Huperzia carinata (Poir.) Trevis Thạch tùng sóng K C - T 4 Huperzia squarrosa (Forst.) Trevis Thạch tùng vảy K T 12 Huperzia obvalifolia (Bon.) Thạch tùng xoan ngược K C - T 8 Huperzia phlegmaria (L.) Roth Râu cây K C - T 9 Lycopodiella cernua (L.) Franco & Vasc Thạch tùng nghiên K T 16 Lycopodiella sp. Thạch tùng K T Selaginellaceae spikemosses 2. HỌ QUYỂN BÁ Selaginella delicatula (Desv) Alst. Quyển bá yếu K T 41 Selaginella rolandi-principis Alston. Hoa đá K T 27 Selaginella willdenowii (Desv.) Baker. Quyển bá Willdenov K T 33 Selaginella chrysorrhizos Spring Quyển bá vàng K 39 Selaginella minutifolia Spring Quyển bá vi diệp K 49 (Division) Pteridophyta (Polypodiophyta) Leptosporangiate ferns Ngành Dương xỉ Class: Marattiopsida Lớp Dương xỉ tòa sen Marattiaceae (prev. Angiopteridaceae) 4. HỌ HIỀN DỰC Angiopteris repandulade Vriese. Ráng hiền dực K 82 Class: Pteridopsida or Polypodiopsida Lớp Dương xỉ Order: Polypodiales polypod ferns Bộ Dương xỉ Aspleniaceae 5. HỌ CAN XỈ Asplenium nidus L. Ráng ổ phụng K 456 Asplenium wightii Eatoni Hook. -
Pomacentridae): Structural and Expression Variation in Opsin Genes
Molecular Ecology (2017) 26, 1323–1342 doi: 10.1111/mec.13968 Why UV vision and red vision are important for damselfish (Pomacentridae): structural and expression variation in opsin genes SARA M. STIEB,*† FABIO CORTESI,*† LORENZ SUEESS,* KAREN L. CARLETON,‡ WALTER SALZBURGER† and N. J. MARSHALL* *Sensory Neurobiology Group, Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia, †Zoological Institute, University of Basel, Basel 4051, Switzerland, ‡Department of Biology, The University of Maryland, College Park, MD 20742, USA Abstract Coral reefs belong to the most diverse ecosystems on our planet. The diversity in col- oration and lifestyles of coral reef fishes makes them a particularly promising system to study the role of visual communication and adaptation. Here, we investigated the evolution of visual pigment genes (opsins) in damselfish (Pomacentridae) and exam- ined whether structural and expression variation of opsins can be linked to ecology. Using DNA sequence data of a phylogenetically representative set of 31 damselfish species, we show that all but one visual opsin are evolving under positive selection. In addition, selection on opsin tuning sites, including cases of divergent, parallel, conver- gent and reversed evolution, has been strong throughout the radiation of damselfish, emphasizing the importance of visual tuning for this group. The highest functional variation in opsin protein sequences was observed in the short- followed by the long- wavelength end of the visual spectrum. Comparative gene expression analyses of a subset of the same species revealed that with SWS1, RH2B and RH2A always being expressed, damselfish use an overall short-wavelength shifted expression profile. Inter- estingly, not only did all species express SWS1 – a UV-sensitive opsin – and possess UV-transmitting lenses, most species also feature UV-reflective body parts. -
Scleractinia Fauna of Taiwan I
Scleractinia Fauna of Taiwan I. The Complex Group 台灣石珊瑚誌 I. 複雜類群 Chang-feng Dai and Sharon Horng Institute of Oceanography, National Taiwan University Published by National Taiwan University, No.1, Sec. 4, Roosevelt Rd., Taipei, Taiwan Table of Contents Scleractinia Fauna of Taiwan ................................................................................................1 General Introduction ........................................................................................................1 Historical Review .............................................................................................................1 Basics for Coral Taxonomy ..............................................................................................4 Taxonomic Framework and Phylogeny ........................................................................... 9 Family Acroporidae ............................................................................................................ 15 Montipora ...................................................................................................................... 17 Acropora ........................................................................................................................ 47 Anacropora .................................................................................................................... 95 Isopora ...........................................................................................................................96 Astreopora ......................................................................................................................99 -
AC26 Doc. 20 Annex 6 English Only / Únicamente En Inglés / Seulement En Anglais
AC26 Doc. 20 Annex 6 English only / únicamente en inglés / seulement en anglais Annex 6 CORAL SPECIES, SYNONYMS, AND NOMENCLATURE REFERENCES CURRENTLY RECOGNIZED IN THE UNEP-WCMC DATABASE Data kindly provided by UNEP-WCMC AC26 Doc. 20, Annex 6 – 1 AC26 Doc. 20 Annex 6 English only / únicamente en inglés / seulement en anglais CORAL SPECIES AND SYNONYMS CURRENTLY RECOGNIZED IN THE UNEP‐WCMC DATABASE 1. Scleractinia families FamName Accepted Name SpcAuthor Nomenclature Reference Synonyms ACROPORIDAE Acropora abrolhosensis Veron, 1985 Veron (2000) Acropora mangarevensis; Madrepora ACROPORIDAE Acropora abrotanoides (Lamarck, 1816) Veron (2000) crassa; Madrepora abrotanoides ACROPORIDAE Acropora aculeus (Dana, 1846) Veron (2000) Madrepora aculeus Acropora diffusa; Madrepora acuminata; ACROPORIDAE Acropora acuminata (Verrill, 1864) Veron (2000) Madrepora diffusa; Madrepora nigra ACROPORIDAE Acropora akajimensis Veron, 1990 Veron (2000) Madrepora anthocercis; Madrepora ACROPORIDAE Acropora anthocercis (Brook, 1893) Veron (2000) coronata ACROPORIDAE Acropora arabensis Hodgson & Carpenter, 1995 Veron (2000) Acropora cribripora; Acropora hebes; Acropora manni; Acropora yaeyamaensis; ACROPORIDAE Acropora aspera (Dana, 1846) Veron (2000) Madrepora aspera; Madrepora cribripora; Madrepora hebes; Madrepora manni ACROPORIDAE Acropora austera (Dana, 1846) Veron (2000) Madrepora austera ACROPORIDAE Acropora awi Wallace & Wolstenholme, 1998 Veron (2000) ACROPORIDAE Acropora azurea Veron & Wallace, 1984 Veron (2000) ACROPORIDAE Acropora batunai Wallace,