I Annotated Selected Bibliography
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Carmona Retusa Carmona Boraginaceae
Carmona retusa Carmona Boraginaceae Forest Starr, Kim Starr, and Lloyd Loope United States Geological Survey--Biological Resources Division Haleakala Field Station, Maui, Hawai'i January, 2003 OVERVIEW Carmona retusa is a popular ornamental plant cultivated in Hawai'i as a hedge or specimen plant. On Maui, C. retusa is observed in residential plantings, mostly in low elevation neighborhoods, such as Kahului, Wailuku, Lahaina, Paia, Haiku, and Kihei. Seedlings and naturalized plants are also commonly observed in landscaping areas and wild semi-wild areas nearby plantings. In one area in Waiehu, C. retusa forms a dense shrubby understory in a kiawe (Prosopis pallida) forest. This plant is fairly widespread on Maui and is probably beyond the eradication stage. Future efforts should be aimed at monitoring, preventing infestations in natural areas, and educating the public about harmful plants that spread beyond the confines of the garden. TAXONOMY Family: Boraginaceae (Heliotrope family) (Lorence et al. 1995, Wagner et al. 1999). Latin name: Carmona retusa (Vahl) Masamune (Lorence et al. 1995, Wagner et al. 1999). Synonyms: C. microphylla (Lam.) Don; Ehretia microphylla Lam.; Ehretia buxifolia Roxb.; Cordia retusa Vahl (Lorence et al. 1995; Bailey and Bailey 1976; GRIN 2001). Common names: Carmona, Philippine tea (Bailey and Bailey 1976), Fukien tea (Caine and Zane 2001). Taxonomic notes: The genus Carmona, also commonly known as Ehretia, is comprised of about 50 species of evergreen or deciduous shrubs and trees of tropical and subtropical regions of both the New and Old World (Bailey and Bailey 1976). Related species in Hawai'i: Neal (1965) lists Ehretia acuminata R. -
CGGJ Vansteenis
BIBLIOGRAPHY : ALGAE 3957 X. Bibliography C.G.G.J. van Steenis (continued from page 3864) The entries have been split into five categories: a) Algae — b) Fungi & Lichens — c) Bryophytes — d) Pteridophytes — e) Spermatophytes 8 General subjects. — Books have been marked with an asterisk. a) Algae: ABDUS M & Ulva a SALAM, A. Y.S.A.KHAN, patengansis, new species from Bang- ladesh. Phykos 19 (1980) 129-131, 4 fig. ADEY ,w. H., R.A.TOWNSEND & w„T„ BOYKINS, The crustose coralline algae (Rho- dophyta: Corallinaceae) of the Hawaiian Islands. Smithson„Contr„ Marine Sci. no 15 (1982) 1-74, 47 fig. 10 new) 29 new); to subfamilies and genera (1 and spp. (several key genera; keys to species„ BANDO,T„, S.WATANABE & T„NAKANO, Desmids from soil of paddyfields collect- ed in Java and Sumatra. Tukar-Menukar 1 (1982) 7-23, 4 fig. 85 species listed and annotated; no novelties. *CHRISTIANSON,I.G., M.N.CLAYTON & B.M.ALLENDER (eds.), B.FUHRER (photogr.), Seaweeds of Australia. A.H.& A.W.Reed Pty Ltd., Sydney (1981) 112 pp., 186 col.pl. Magnificent atlas; text only with the phyla; ample captions; some seagrasses included. CORDERO Jr,P.A„ Studies on Philippine marine red algae. Nat.Mus.Philip., Manila (1981) 258 pp., 28 pi., 1 map, 265 fig. Thesis (Kyoto); keys and descriptions of 259 spp„, half of them new to the Philippines; 1 new species. A preliminary study of the ethnobotany of Philippine edible sea- weeds, especially from Ilocos Norte and Cagayan Provinces. Acta Manillana A 21 (31) (1982) 54-79. Chemical analysis; scientific and local names; indication of uses and storage. -
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. -
Sistema De Clasificación Artificial De Las Magnoliatas Sinántropas De Cuba
Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA Pedro- Pabfc He.r retira Qltver CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA Y UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA ASPIRANTE: Lie. Pedro Pablo Herrera Oliver Investigador Auxiliar Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente DIRECTORES: CUBA Dra. Nancy Esther Ricardo Ñapóles Investigador Titular Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente ESPAÑA Dr. Andreu Bonet Jornet Piiofesjar Titular Departamento de EGdfegfe Universidad! dte Mearte CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver I. INTRODUCCIÓN 1 II. ANTECEDENTES 6 2.1 Historia de los esquemas de clasificación de las especies sinántropas (1903-2005) 6 2.2 Historia del conocimiento de las plantas sinantrópicas en Cuba 14 III. -
A New Record of Ehretia (Ehretiaceae, Boraginales) for Thailand
THAI FOREST BULL., BOT. 47(1): 34–37. 2019. DOI https://doi.org/10.20531/tfb.2019.47.1.07 A new record of Ehretia (Ehretiaceae, Boraginales) for Thailand KANOKORN RUEANGSAWANG1,*, MANOP POOPATH2 & PRANOM CHANTARANOTHAI3 ABSTRACT Ehretia silvana, a tree from limestone habitat in Uthai Thani province, is newly recorded for Thailand. A description and illustrations are provided, together with a conservation assessment and a new key to the species of Ehretia in Thailand. KEYWORDS: Ehretia silvana, conservation assessment, taxonomy Accepted for publication: 25 February 2019. Published online: 25 March 2019 INTRODUCTION specimen [K001110196], designated by Mill, 1996; isolectotypes BM! [BM000603166], K! [K000998072], Ehretia P.Br. has a pantropical distribution and M! [M0188691, M0188692]). Figs. 1–2. comprises ca 50 species of trees to shrubs. The genus, formerly in Boraginaceae subfam. Ehretioideae, is Trees, 3–7 m tall; bark thin, rough, grey-brown, now classified under Ehretiaceae (Boraginales), and with elliptic lenticels, glabrous; branchlets terete, is distinguished by having a bifid style with two glabrous to sparsely puberulous with glandular stigmatic branches and drupaceous fruits with four trichomes when young. Leaves chartaceous, elliptic pyrenes (Gottschling & Hilger, 2004; Luebert et al., to broadly ovate, 12–18 × 7–12 cm, apex cuspidate 2016). This circumscription of the family is supported or acuminate, base oblique or rounded, margin entire; by molecular analysis using nrITS and cpDNA upper surface dark green, glabrous, lustrous; lower sequence data (Gottschling et al., 2014). Five species surface light green, usually puberulous, with scattered were enumerated in the most recent treatment of the in the axils of lateral veins or glandular trichomes genus for Thailand by Ruengsawang & Chantaranothai when young; lateral veins and venations impressed (2010), then still under Boraginaceae. -
Notes from Grasses Workshop
NATIVE GRASSES OF THE MELBOURNE AREA WORKSHOP AT BRIMBANK PARK March 25, 1988 For the Melbourne and Metropolitan Board of Works By Paget and Shim m en Bushland Seeds (14 Seascape Close, FTG 3156. PH:758.5416) INTRODUCTION: Native Grasses covers a wide range of grass species, of wkich there are . species suital~le for a variety of uses, induding erosion control, lawns, parklands, coastal sand dune stabilization, and low fire-hazard plantings. Most grasslands in Victoria are now exotic pastures, co m posed of grasses which have been bred for high l~iomass product5on so they produce Large a mounts of feed for stock, and these grasses are usually winter-growing and die-back severely over sum m er. These sa m e grasses do not necessarily have the rn ost desired characteristics for those orher uses. In lawns, for example, high biomass production means regular mowing, and growing in winter m cans they browning off during summer. Many of our native grasses are not as vigorous and grow over sum mcr, so do not grow so fast as to require constant mowing, and do not brown off over summer. ATTRIBUTES: The above introduction is a broad generalization, and it is important Lo study the charactemcs of each grass species to determine both its suitabtkity for any use, and the manage rn cnt it: requires. The most important attribute to contider is that of the grass's growth period. The table below ouflines the growth periods of the major native grass species: COMMON NAME BOTANICAL NAME GROWS COMMON WHEAT-GRASS A gropyron scabru m Winter COMMON BLOWN GRASS -
Revision of the Genus Cleidion (Euphorbiaceae) in Malesia
BLUMEA 50: 197–219 Published on 22 April 2005 http://dx.doi.org/10.3767/000651905X623373 REVISION OF THE GENUS CLEIDION (EUPHORBIACEAE) IN MALESIA KRISTO K.M. KULJU & PETER C. VAN WELZEN Nationaal Herbarium Nederland, Universiteit Leiden branch, P.O. Box 9514, 2300 RA Leiden, The Netherlands; e-mail: [email protected], [email protected] SUMMARY A revision of the Malesian species in the genus Cleidion is presented. Cleidion javanicum is shown to be the correct name for the widespread type species (instead of the name C. spiciflorum). A new species, C. luziae, resembling C. javanicum, is described from the Moluccas, New Guinea and the Solomon Islands. In addition, C. salomonis is synonymised with C. papuanum and C. lanceolatum is treated as a variety of C. ramosii. In total 7 Malesian Cleidion species are recognized. Cleidion megistophyllum from the Philippines cannot reliably be confirmed to belong to the genus due to lack of information and specimens and is treated as a doubtful species. Key words: Cleidion, Acalypheae, Cleidiinae, revision, taxonomy, Malesia. INTRODUCTION Cleidion is a pantropical genus belonging to the large angiosperm family Euphorbiaceae s.s. It was described by Blume (1825), who included a single species C. javanicum1. The first revision was made by Müller Argoviensis (1865, 1866). His work was fol- lowed by the comprehensive treatment of Pax & Hoffmann (1914), which included 17 species. Pax & Hoffmann excluded the section Discocleidion Müll.Arg. which differs from Cleidion by the presence of a staminate and pistillate disc (in Cleidion a disc is absent), stipellate and palmatinerved leaves (in Cleidion the leaves are non-stipellate and pinnatinerved), and differences in anther type. -
Title Evolutionary Relationships Between Pollination and Protective Mutualisms in the Genus Macaranga (Euphorbiaceae)( Dissertat
Evolutionary relationships between pollination and protective Title mutualisms in the genus Macaranga (Euphorbiaceae)( Dissertation_全文 ) Author(s) Yamasaki, Eri Citation 京都大学 Issue Date 2014-03-24 URL https://doi.org/10.14989/doctor.k18113 学位規則第9条第2項により要約公開; 許諾条件により本文 Right は2019-06-25に公開 Type Thesis or Dissertation Textversion ETD Kyoto University Evolutionary relationships between pollination and protective mutualisms in the genus Macaranga (Euphorbiaceae) Eri Yamasaki 2014 1 2 Contents 摘要.…………………………………………………………………………………..5 Summary.……………………………………………………………………………..9 Chapter 1 General introduction……………………………………………………………….14 Chapter 2 Diversity of pollination systems in Macaranga Section 2.1 Diversity of bracteole morphology in Macaranga ………………………….20 Section 2.2 Wind and insect pollination (ambophily) in Mallotus , a sister group of Macaranga …………..…………..……...…………..………………………...31 Section 2.3 Disk-shaped nectaries on bracteoles of Macaranga sinensis provide a reward for pollinators……………………………….………………………………...45 Chapter 3 Interactions among plants, pollinators and guard ants in ant-plant Macaranga Section 3.1 Density of ant guards on inflorescences and their effects on herbivores and pollinators…………………………………………………….......................56 Section 3.2 Anal secretions of pollinator thrips of Macaranga winkleri repel guard ants…….71 Chapter 4 General discussion.………………….……………………………………………...85 Appendix…………………………………………………………………….………89 Acknowledgement…………………………………………………………….…...101 Literature cited……………………………….…………………………………….103 -
Lecythidaceae (G.T
Flora Malesiana, Series I, Volume 21 (2013) 1–118 LECYTHIDACEAE (G.T. Prance, Kew & E.K. Kartawinata, Bogor)1 Lecythidaceae A.Rich. in Bory, Dict. Class. Hist. Nat. 9 (1825) 259 (‘Lécythidées’), nom. cons.; Poit., Mém. Mus. Hist. Nat. Paris 13 (1835) 141; Miers, Trans. Linn. Soc. London, Bot. 30, 2 (1874) 157; Nied. in Engl. & Prantl, Nat. Pflanzenfam. 3, 7 (1892) 30; R.Knuth in Engl., Pflanzenr. IV.219, Heft 105 (1939) 26; Whitmore, Tree Fl. Malaya 2 (1973) 257; R.J.F.Hend., Fl. Australia 8 (1982) 1; Corner, Wayside Trees Malaya ed. 3, 1 (1988) 349; S.A.Mori & Prance, Fl. Neotrop. Monogr. 21, 2 (1990) 1; Chantar., Kew Bull. 50 (1995) 677; Pinard, Tree Fl. Sabah & Sarawak 4 (2002) 101; H.N.Qin & Prance, Fl. China 13 (2007) 293; Prance in Kiew et al., Fl. Penins. Malaysia, Ser. 2, 3 (2012) 175. — Myrtaceae tribus Lecythideae (A.Rich.) A.Rich. ex DC., Prodr. 3 (1828) 288. — Myrtaceae subtribus Eulecythideae Benth. & Hook.f., Gen. Pl. 1, 2 (1865) 695, nom. inval. — Type: Lecythis Loefl. Napoleaeonaceae A.Rich. in Bory, Dict. Class. Hist. Nat. 11 (1827) 432. — Lecythi- daceae subfam. Napoleonoideae Nied. in Engl. & Prantl., Nat. Pflanzenfam. 3, 7 (1893) 33. — Type: Napoleonaea P.Beauv. Scytopetalaceae Engl. in Engl. & Prantl, Nat. Pflanzenfam., Nachtr. 1 (1897) 242. — Lecythidaceae subfam. Scytopetaloideae (Engl.) O.Appel, Bot. J. Linn. Soc. 121 (1996) 225. — Type: Scytopetalum Pierre ex Engl. Lecythidaceae subfam. Foetidioideae Nied. in Engl. & Prantl, Nat Pflanzenfam. 3, 7 (1892) 29. — Foetidiaceae (Nied.) Airy Shaw in Willis & Airy Shaw, Dict. Fl. Pl., ed. -
Flora and Fauna
ENVIRONMENTAL ASSESSMENT Volume 2 Technical Papers MUNMORAH GAS TURBINE FACILITY MUNMORAH POWER STATION.indd 3 21/12/05 2:27:29 PM Contents Technical Papers (Volume 2) Technical Paper No.1 Flora and Fauna Assessment Technical Paper No.2 Heritage Assessment Technical Paper No.3 Noise Assessment Technical Paper No.4 Air Quality Impact Assessment Technical Paper No 5 Photochemical Pollution Assessment Technical Paper No 6 Preliminary Hazard Analysis FLORA AND FAUNA ASSESSMENT TECHNICAL PAPER DIVIDERS.indd 30 121/12/05 3:44:33 PM Technical Paper 1 Flora and Fauna Assessment of Munmorah Gas Turbine Facility December 2005 Delta Electricity Parsons Brinckerhoff Australia Pty Limited ACN 078 004 798 and Parsons Brinckerhoff International (Australia) Pty Limited ACN 006 475 056 trading as Parsons Brinckerhoff ABN 84 797 323 433 Level 27 Ernst & Young Centre 680 George Street Sydney NSW 2000 GPO Box 5394 Australia Telephone +61 2 9272 5100 Facsimile +61 2 9272 5101 Email [email protected] ABN 84 797 323 433 NCSI Certified Quality System ISO 9001 2116541A Parsons Brinckerhoff supports the Environment by PR_2467.doc printing on 100per cent A4 recycled paper ©Parsons Brinckerhoff Australia Pty Limited and Parsons Brinckerhoff International (Australia) Pty Limited trading as Parsons Brinckerhoff (“PB”). [2005] Copyright in the drawings, information and data recorded in this document (“the information”) is the property of PB. This document and the information are solely for the use of the authorised recipient and this document may not be used, copied or reproduced in whole or part for any purpose other than that for which it was supplied by PB. -
ABSTRACTS 117 Systematics Section, BSA / ASPT / IOPB
Systematics Section, BSA / ASPT / IOPB 466 HARDY, CHRISTOPHER R.1,2*, JERROLD I DAVIS1, breeding system. This effectively reproductively isolates the species. ROBERT B. FADEN3, AND DENNIS W. STEVENSON1,2 Previous studies have provided extensive genetic, phylogenetic and 1Bailey Hortorium, Cornell University, Ithaca, NY 14853; 2New York natural selection data which allow for a rare opportunity to now Botanical Garden, Bronx, NY 10458; 3Dept. of Botany, National study and interpret ontogenetic changes as sources of evolutionary Museum of Natural History, Smithsonian Institution, Washington, novelties in floral form. Three populations of M. cardinalis and four DC 20560 populations of M. lewisii (representing both described races) were studied from initiation of floral apex to anthesis using SEM and light Phylogenetics of Cochliostema, Geogenanthus, and microscopy. Allometric analyses were conducted on data derived an undescribed genus (Commelinaceae) using from floral organs. Sympatric populations of the species from morphology and DNA sequence data from 26S, 5S- Yosemite National Park were compared. Calyces of M. lewisii initi- NTS, rbcL, and trnL-F loci ate later than those of M. cardinalis relative to the inner whorls, and sepals are taller and more acute. Relative times of initiation of phylogenetic study was conducted on a group of three small petals, sepals and pistil are similar in both species. Petal shapes dif- genera of neotropical Commelinaceae that exhibit a variety fer between species throughout development. Corolla aperture of unusual floral morphologies and habits. Morphological A shape becomes dorso-ventrally narrow during development of M. characters and DNA sequence data from plastid (rbcL, trnL-F) and lewisii, and laterally narrow in M. -
Everywhere but Antarctica: Using a Super Tree to Understand the Diversity and Distribution of the Compositae
BS 55 343 Everywhere but Antarctica: Using a super tree to understand the diversity and distribution of the Compositae VICKI A. FUNK, RANDALL J. BAYER, STERLING KEELEY, RAYMUND CHAN, LINDA WATSON, BIRGIT GEMEINHOLZER, EDWARD SCHILLING, JOSE L. PANERO, BRUCE G. BALDWIN, NURIA GARCIA-JACAS, ALFONSO SUSANNA AND ROBERT K. JANSEN FUNK, VA., BAYER, R.J., KEELEY, S., CHAN, R., WATSON, L, GEMEINHOLZER, B., SCHILLING, E., PANERO, J.L., BALDWIN, B.G., GARCIA-JACAS, N., SUSANNA, A. &JANSEN, R.K 2005. Everywhere but Antarctica: Using a supertree to understand the diversity and distribution of the Compositae. Biol. Skr. 55: 343-374. ISSN 0366-3612. ISBN 87-7304-304-4. One of every 10 flowering plant species is in the family Compositae. With ca. 24,000-30,000 species in 1600-1700 genera and a distribution that is global except for Antarctica, it is the most diverse of all plant families. Although clearly mouophyletic, there is a great deal of diversity among the members: habit varies from annual and perennial herbs to shrubs, vines, or trees, and species grow in nearly every type of habitat from lowland forests to the high alpine fell fields, though they are most common in open areas. Some are well-known weeds, but most species have restricted distributions, and members of this family are often important components of 'at risk' habitats as in the Cape Floral Kingdom or the Hawaiian Islands. The sub-familial classification and ideas about major patterns of evolution and diversification within the family remained largely unchanged from Beutham through Cronquist. Recently obtained data, both morphologi- cal and molecular, have allowed us to examine the distribution and evolution of the family in a way that was never before possible.