Dipentodon. a New Genus of Uncertain Systematic Position Author(S): S
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Kamakahala Labordia Cyrtandrae
No Photo Available Plants Kamakahala Labordia cyrtandrae Federally Listed as Endangered Genetic Safety Net Species IUCN Red List Ranking – Critically Endangered (CR D) Hawai‘i Natural Heritage Ranking ‐ Critically Imperiled (G1) Endemism – O‘ahu Critical Habitat ‐ Designated SPECIES INFORMATION: Labordia cyrtandrae, a short‐lived perennial member of the logania family (Loganiaceae), is a shrub 0.7 to 2 m (2.3 to 6.6 ft) tall. This species is distinguished from others in the genus by its fleshy, hairy, cylindrical stem that flattens upon drying, the shape and length of the floral bracts, and the length of the corolla tube and lobes. Labordia cyrtandrae has been observed flowering from May through June, fruiting from July through August, and is sporadically fertile year‐round. The flowers are functionally unisexual, and male and female flowers are on separate plants. DISTRIBUTION: Labordia cyrtandrae is endemic to the Wai‘anae Mountains and Ko‘olau Mountains of O‘ahu. ABUNDANCE: Currently there are four subpopulations known, totaling 11 individuals. LOCATION AND CONDITION OF KEY HABITAT: Labordia cyrtandrae typically grows in shady gulches, slopes, and glens in mesic to wet forests and shrublands dominated by Metrosideros polymorpha, Diplopterygium pinnatum, and/or Acacia koa between the elevations of 212 and 1,233 m (695 and 4,044 ft). The habitat of Labordia cyrtandrae has been degraded by feral pigs; competition with the alien plants such as Christmas berry, Koster’s curse, prickly Florida blackberry, and strawberry guava, and is potentially threatened by military activities and fire. Associated native plant species include Antidesma sp., Artemisia australis, Bidens torta, Boehmeria grandis, Broussaisia arguta, Chamaesyce sp., Coprosma sp., Cyrtandra sp., Dicranopteris linearis, Diplazium sandwichianum, Dubautia plantaginea (naenae), Lysimachia hillebrandii, Peperomia membranacea (ala ala wai nui), Perrottetia sandwicensis, Phyllostegia sp., Pipturus albidus, Pouteria sandwicensis, and Psychotria sp. -
A Landscape-Based Assessment of Climate Change Vulnerability for All Native Hawaiian Plants
Technical Report HCSU-044 A LANDscape-bASED ASSESSMENT OF CLIMatE CHANGE VULNEraBILITY FOR ALL NatIVE HAWAIIAN PLANts Lucas Fortini1,2, Jonathan Price3, James Jacobi2, Adam Vorsino4, Jeff Burgett1,4, Kevin Brinck5, Fred Amidon4, Steve Miller4, Sam `Ohukani`ohi`a Gon III6, Gregory Koob7, and Eben Paxton2 1 Pacific Islands Climate Change Cooperative, Honolulu, HI 96813 2 U.S. Geological Survey, Pacific Island Ecosystems Research Center, Hawaii National Park, HI 96718 3 Department of Geography & Environmental Studies, University of Hawai‘i at Hilo, Hilo, HI 96720 4 U.S. Fish & Wildlife Service —Ecological Services, Division of Climate Change and Strategic Habitat Management, Honolulu, HI 96850 5 Hawai‘i Cooperative Studies Unit, Pacific Island Ecosystems Research Center, Hawai‘i National Park, HI 96718 6 The Nature Conservancy, Hawai‘i Chapter, Honolulu, HI 96817 7 USDA Natural Resources Conservation Service, Hawaii/Pacific Islands Area State Office, Honolulu, HI 96850 Hawai‘i Cooperative Studies Unit University of Hawai‘i at Hilo 200 W. Kawili St. Hilo, HI 96720 (808) 933-0706 November 2013 This product was prepared under Cooperative Agreement CAG09AC00070 for the Pacific Island Ecosystems Research Center of the U.S. Geological Survey. Technical Report HCSU-044 A LANDSCAPE-BASED ASSESSMENT OF CLIMATE CHANGE VULNERABILITY FOR ALL NATIVE HAWAIIAN PLANTS LUCAS FORTINI1,2, JONATHAN PRICE3, JAMES JACOBI2, ADAM VORSINO4, JEFF BURGETT1,4, KEVIN BRINCK5, FRED AMIDON4, STEVE MILLER4, SAM ʽOHUKANIʽOHIʽA GON III 6, GREGORY KOOB7, AND EBEN PAXTON2 1 Pacific Islands Climate Change Cooperative, Honolulu, HI 96813 2 U.S. Geological Survey, Pacific Island Ecosystems Research Center, Hawaiʽi National Park, HI 96718 3 Department of Geography & Environmental Studies, University of Hawaiʽi at Hilo, Hilo, HI 96720 4 U. -
P020110307527551165137.Pdf
CONTENT 1.MESSAGE FROM DIRECTOR …………………………………………………………………………………………………………………………………………………… 03 2.ORGANIZATION STRUCTURE …………………………………………………………………………………………………………………………………………………… 05 3.HIGHLIGHTS OF ACHIEVEMENTS …………………………………………………………………………………………………………………………………………… 06 Coexistence of Conserve and Research----“The Germplasm Bank of Wild Species ” services biodiversity protection and socio-economic development ………………………………………………………………………………………………………………………………………………… 06 The Structure, Activity and New Drug Pre-Clinical Research of Monoterpene Indole Alkaloids ………………………………………… 09 Anti-Cancer Constituents in the Herb Medicine-Shengma (Cimicifuga L) ……………………………………………………………………………… 10 Floristic Study on the Seed Plants of Yaoshan Mountain in Northeast Yunnan …………………………………………………………………… 11 Higher Fungi Resources and Chemical Composition in Alpine and Sub-alpine Regions in Southwest China ……………………… 12 Research Progress on Natural Tobacco Mosaic Virus (TMV) Inhibitors…………………………………………………………………………………… 13 Predicting Global Change through Reconstruction Research of Paleoclimate………………………………………………………………………… 14 Chemical Composition of a traditional Chinese medicine-Swertia mileensis……………………………………………………………………………… 15 Mountain Ecosystem Research has Made New Progress ………………………………………………………………………………………………………… 16 Plant Cyclic Peptide has Made Important Progress ………………………………………………………………………………………………………………… 17 Progresses in Computational Chemistry Research ………………………………………………………………………………………………………………… 18 New Progress in the Total Synthesis of Natural Products ……………………………………………………………………………………………………… -
Phylogeographical Structure of Liquidambar Formosana Hance Revealed by Chloroplast Phylogeography and Species Distribution Models
Article Phylogeographical Structure of Liquidambar formosana Hance Revealed by Chloroplast Phylogeography and Species Distribution Models 1,2, 1, 1 2 1 1, Rongxi Sun y , Furong Lin y, Ping Huang , Xuemin Ye , Jiuxin Lai and Yongqi Zheng * 1 State Key Laboratory of Tree Genetics and Breeding, Key Laboratory of Silviculture of the State Forestry Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 100091, China; [email protected] (R.S.); [email protected] (F.L.); [email protected] (P.H.); [email protected] (J.L.) 2 Jiangxi Provincial Key Laboratory of Silviculture, College of Forestry, Jiangxi Agricultural University, Nanchang 330045, China; [email protected] * Correspondence: [email protected]; Tel.: +86-10-6288-8565 These authors contributed equally to this work. y Received: 2 September 2019; Accepted: 29 September 2019; Published: 1 October 2019 Abstract: To understand the origin and evolutionary history, and the geographical and historical causes for the formation of the current distribution pattern of Lquidambar formosana Hance, we investigated the phylogeography by using chloroplasts DNA (cpDNA) non-coding sequences and species distribution models (SDM). Four cpDNA intergenic spacer regions were amplified and sequenced for 251 individuals from 25 populations covering most of its geographical range in China. A total of 20 haplotypes were recovered. The species had a high level of chloroplast genetic variation (Ht = 0.909 0.0192) and a significant phylogeographical structure (genetic differentiation takes into ± account distances among haplotypes (Nst) = 0.730 > population differentiation that does not consider distances among haplotypes (Gst) = 0.645; p < 0.05), whereas the genetic variation within populations (Hs = 0.323 0.0553) was low. -
Ancistrocladaceae
Soltis et al—American Journal of Botany 98(4):704-730. 2011. – Data Supplement S2 – page 1 Soltis, Douglas E., Stephen A. Smith, Nico Cellinese, Kenneth J. Wurdack, David C. Tank, Samuel F. Brockington, Nancy F. Refulio-Rodriguez, Jay B. Walker, Michael J. Moore, Barbara S. Carlsward, Charles D. Bell, Maribeth Latvis, Sunny Crawley, Chelsea Black, Diaga Diouf, Zhenxiang Xi, Catherine A. Rushworth, Matthew A. Gitzendanner, Kenneth J. Sytsma, Yin-Long Qiu, Khidir W. Hilu, Charles C. Davis, Michael J. Sanderson, Reed S. Beaman, Richard G. Olmstead, Walter S. Judd, Michael J. Donoghue, and Pamela S. Soltis. Angiosperm phylogeny: 17 genes, 640 taxa. American Journal of Botany 98(4): 704-730. Appendix S2. The maximum likelihood majority-rule consensus from the 17-gene analysis shown as a phylogram with mtDNA included for Polyosma. Names of the orders and families follow APG III (2009); other names follow Cantino et al. (2007). Numbers above branches are bootstrap percentages. 67 Acalypha Spathiostemon 100 Ricinus 97 100 Dalechampia Lasiocroton 100 100 Conceveiba Homalanthus 96 Hura Euphorbia 88 Pimelodendron 100 Trigonostemon Euphorbiaceae Codiaeum (incl. Peraceae) 100 Croton Hevea Manihot 10083 Moultonianthus Suregada 98 81 Tetrorchidium Omphalea 100 Endospermum Neoscortechinia 100 98 Pera Clutia Pogonophora 99 Cespedesia Sauvagesia 99 Luxemburgia Ochna Ochnaceae 100 100 53 Quiina Touroulia Medusagyne Caryocar Caryocaraceae 100 Chrysobalanus 100 Atuna Chrysobalananaceae 100 100 Licania Hirtella 100 Euphronia Euphroniaceae 100 Dichapetalum 100 -
Ancistrocladaceae
Soltis et al—American Journal of Botany 98(4):704-730. 2011. – Data Supplement S2 – page 1 Soltis, Douglas E., Stephen A. Smith, Nico Cellinese, Kenneth J. Wurdack, David C. Tank, Samuel F. Brockington, Nancy F. Refulio-Rodriguez, Jay B. Walker, Michael J. Moore, Barbara S. Carlsward, Charles D. Bell, Maribeth Latvis, Sunny Crawley, Chelsea Black, Diaga Diouf, Zhenxiang Xi, Catherine A. Rushworth, Matthew A. Gitzendanner, Kenneth J. Sytsma, Yin-Long Qiu, Khidir W. Hilu, Charles C. Davis, Michael J. Sanderson, Reed S. Beaman, Richard G. Olmstead, Walter S. Judd, Michael J. Donoghue, and Pamela S. Soltis. Angiosperm phylogeny: 17 genes, 640 taxa. American Journal of Botany 98(4): 704-730. Appendix S2. The maximum likelihood majority-rule consensus from the 17-gene analysis shown as a phylogram with mtDNA included for Polyosma. Names of the orders and families follow APG III (2009); other names follow Cantino et al. (2007). Numbers above branches are bootstrap percentages. 67 Acalypha Spathiostemon 100 Ricinus 97 100 Dalechampia Lasiocroton 100 100 Conceveiba Homalanthus 96 Hura Euphorbia 88 Pimelodendron 100 Trigonostemon Euphorbiaceae Codiaeum (incl. Peraceae) 100 Croton Hevea Manihot 10083 Moultonianthus Suregada 98 81 Tetrorchidium Omphalea 100 Endospermum Neoscortechinia 100 98 Pera Clutia Pogonophora 99 Cespedesia Sauvagesia 99 Luxemburgia Ochna Ochnaceae 100 100 53 Quiina Touroulia Medusagyne Caryocar Caryocaraceae 100 Chrysobalanus 100 Atuna Chrysobalananaceae 100 100 Licania Hirtella 100 Euphronia Euphroniaceae 100 Dichapetalum 100 -
Title the Noroshi Flora of Note Peninsula, Central Japan Author(S)
Title The Noroshi Flora of Note Peninsula, Central Japan Author(s) Ishida, Shiro Memoirs of the Faculty of Science, Kyoto University. Series of Citation geology and mineralogy (1970), 37(1): 1-112 Issue Date 1970-12-15 URL http://hdl.handle.net/2433/186566 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University MEMolRs oF THE FAcvLTy oF SclENcE, KyoTo UNIvlsRsrTy, SERIEs oF GEoL. & MINERAL. Vol. XXXVII, No. 1, pp. 1-112, pls. 1-22, December 15, 1970 The Noroshi Flora of Noto Peninsula, Central Japan By Shiro IsHiDA (Received December 20, 1969) CONTENTS Page Abstract ................................................................................... 3 . The Noroshi Flora .....................................................,................. 3 . Introduction .......,.........................................•••••••••••••••••••••• 3 . Acknowledgments .......................................................,... tl • Geologic Occurrence .........................................-•••••••••••••••••••• . 4 Composition ....................................................................... 12 . Systematic List of Families and Species ................................ 13 . List of Microfossils .................,......................................... 16 . Numerical Representation .................................................. 17 . Paleoecology ......................................................................• 21 Physical Conditions Indicated by the Flora .......................... 21 - Distributional Considerations -
Dipentodontaceae*
FLORA DEL BAJÍO Y DE REGIONES ADYACENTES Fascículo 169 febrero de 2011 DIPENTODONTACEAE* Por María Eugenia Molina-Paniagua**,*** Instituto de Ecología, A.C. Centro Regional del Bajío Pátzcuaro, Michoacán y Francisco G. Lorea-Hernández Instituto de Ecología, A.C. Xalapa, Veracruz. Árboles o arbustos hermafroditas o dioicos, perennifolios o caducifolios; hojas simples, alternas, pecioladas, estípulas pequeñas, caducas, venación pinnada; in- florescencia axilar o terminal, cimosa, tirsoide o umbelada; flores pequeñas, (4)5(7)- * Referencias: Cronquist, A. An integrated system of classification of flowering plants. Columbia University Press. New York. 681 pp. 1981. Ma, J. & B. Bartholomew. Dipentodontaceae. In: Wu, Z. & P. H. Raven. (eds.). Flora of China 11: 494- 495. 2008. Matthews, M. L. & P. K. Endress. Comparative floral structure and systematics of Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae). Botanical Journal of the Linnean Society 149: 129- 194. 2005. Simmons, M. P. Celastraceae. In: Kubitzki, K. (ed.). The families and genera of vascular plants. VI. Flowering plants. Dicotyledons: Celastrales, Oxalidales, Rosales, Cornales, Ericales. Springer-Verlag. Berlin & Heidelberg. pp. 27-64. 2004. Worberg, A., M. H. Alford., D. Quandt & T. Borsch. Huerteales sister to Brassicales plus Malvales, and newly circumscribed to include Dipentodon, Gerrardina, Huertea, Perrottetia and Tapiscia. Taxon 58: 468-478. 2009. Zhang, L. B. & M. P. Simmons. Phylogeny and delimitation of the Celastrales inferred from nuclear and plastid genes. Systematic Botany 31: 122-137. 2006. ** Se agradece a los doctores Ma. Hilda Flores, Fernando Chiang, Sergio Zamudio y Jerzy Rzedowski por sus importantes sugerencias para la integración de este trabajo. Se dan las gracias asimismo a la Biól. Paola Rodríguez Torres por la elaboración de la ilustración. -
Taxonomic and Phylogenetic Census of the Celastrales: a Synthetic Review Shisode S.B.1 and D.A
Curr. Bot. 2(4): 36-43, 2011 REVIEW ARTICLE Taxonomic and phylogenetic census of the Celastrales: A synthetic review Shisode S.B.1 and D.A. Patil2 1 Department of Botany L. V. H. College, Panchavati, Nashik–422003 (M.S.) India 2 Post-Graduate Department of Botany S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science College, Dhule – 424 005, India K EYWORDS A BSTRACT Taxonomy, Phylogeny, Celastrales A comprehensive assessment of the taxonomic and phylogenetic status of the celeastralean plexus is presented. An attempt has been made to review synthetically C ORRESPONDENCE based on the data from different disciplines divulged by earlier authors and from present author’s study on the alliance. The taxonomic literature indicated that the D.A. Patil, Post-Graduate Department of Botany Celeastrales (sensu lato) are a loose-knit assemblage. The tribal, subfamilial, familial S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science and even ordinal boundaries are uncertain and even criss-cross each other. It College , Dhule – 424 005, India appeared that the alliance can be grouped under two taxonomic entities viz., the Celastrales and the Rhamnales which appear evolved convergently. E-mail: [email protected] E DITOR Datta Dhale CB Volume 2, Year 2011, Pages 36-43 Introduction Hipporcrateaceae are accorded an independent familial status. The order Celastrales (sensu lato) is a loose - knit The family Rhamnaceae is included under the Rhamnales assemblage. The taxonomic history clearly reflected that this alongwith the Vitaceae only. In the latest Engler's syllabus, alliance is not restricted to any taxonomic entity. -
Forest and Population Structure and Regeneration Dynamics of Relict Dipentodon Sinicus in Southwestern China
Taiwania 64(4): 396-408, 2019 DOI: 10.6165/tai.2019.64.396 Forest and population structure and regeneration dynamics of relict Dipentodon sinicus in southwestern China Cindy Q. TANG1,*, Diao-Shun HUANG1, Peng-Bin HAN1, Li-Qin SHEN1, Yun-Fang LI2,*, Shuaifeng LI3, Qian CHEN4, Zhi-Ying ZHANG1 1. Institute of Ecology and Geobotany, College of Ecology and Environmental Science, Yunnan University, Dongwaihuan South Road, University Town, Chenggong New District, Kunming, Yunnan 650504, China. 2. Caojian Forest Station of Yunlong Forestry Bureau, Caojian Zhen, Yunlong County, Yunnan 672711, China. 3. Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, Yunnan 650224, China. 4. Liupanshui City Twenty-Second Middle School, Renmin Lu, Zhongshan District, Liupanshui, Guizhou 553000, China. *Corresponding author’s emails: Cindy Q. Tang: [email protected]; Yun-Fang Li: [email protected] (Manuscript received 21 May 2019; accepted 24 August 2019; online published 9 September 2019) ABSTRACT: Dipentodon sinicus is an extant relict plant of East Asia. It is a small deciduous broad-leaved tree, the sole surviving representative of the Dipentodonaceae. We investigated forest features, population structure, and regeneration dynamics of forest stands containing this species in Caojian Forest Station of Yunnan Province and Yushe National Forest Parks of Guizhou Province, southwestern China. We identified six forest types: Carpinus kweichowensis-Liquidambar formosana-Lithocarpus glaber- Dipentodon sinicus forest (Type 1); Illicium simonsii-Salix matsudana-Schima khasiana-Dipentodon sinicus forest (Type 2); Dipentodon sinicus forest (Type 3); Dipentodon sinicus-Schima khasiana forest (Type 4); Dipentodon sinicus-Tetracentron sinense forest (Type 5); Pterocarya macroptera var. delavayi-Tetracentron sinense-Populus yunnanensis-Salix matsudana forest (Type 6). -
China: a Rich Flora Needed of Urgent Conservationprovided by Digital.CSIC
Orsis 19, 2004 49-89 View metadata, citation and similar papers at core.ac.uk brought to you by CORE China: a rich flora needed of urgent conservationprovided by Digital.CSIC López-Pujol, Jordi GReB, Laboratori de Botànica, Facultat de Farmàcia, Universitat de Barcelona, Avda. Joan XXIII s/n, E-08028, Barcelona, Catalonia, Spain. Author for correspondence (E-mail: [email protected]) Zhao, A-Man Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, The People’s Republic of China. Manuscript received in april 2004 Abstract China is one of the richest countries in plant biodiversity in the world. Besides to a rich flora, which contains about 33 000 vascular plants (being 30 000 of these angiosperms, 250 gymnosperms, and 2 600 pteridophytes), there is a extraordinary ecosystem diversity. In addition, China also contains a large pool of both wild and cultivated germplasm; one of the eight original centers of crop plants in the world was located there. China is also con- sidered one of the main centers of origin and diversification for seed plants on Earth, and it is specially profuse in phylogenetically primitive taxa and/or paleoendemics due to the glaciation refuge role played by this area in the Quaternary. The collision of Indian sub- continent enriched significantly the Chinese flora and produced the formation of many neoen- demisms. However, the distribution of the flora is uneven, and some local floristic hotspots can be found across China, such as Yunnan, Sichuan and Taiwan. Unfortunately, threats to this biodiversity are huge and have increased substantially in the last 50 years. -
Environmental Assessment
Final Environmental Assessment Kohala Mountain Watershed Management Project Districts of Hāmākua, North Kohala, and South Kohala County of Hawai‘i Island of Hawai‘i In accordance with Chapter 343, Hawai‘i Revised Statutes Proposed by: Kohala Watershed Partnership P.O. Box 437182 Kamuela, HI 96743 October 15, 2008 Table of Contents I. Summary................................................................................................................ .... 3 II. Overall Project Description ................................................................................... .... 6 III. Description of Actions............................................................................................ .. 10 IV. Description of Affected Environments .................................................................. .. 18 V. Summary of Major Impacts and Mitigation Measures........................................... .. 28 VI. Alternatives Considered......................................................................................... .. 35 VII. Anticipated Determination, Reasons Supporting the Anticipated Determination.. .. 36 VIII. List of Permits Required for Project...................................................................... .. 39 IX. Environmental Assessment Preparation Information ............................................ .. 40 X. References ............................................................................................................. .. 40 XI. Appendices ...........................................................................................................