DOCSLIB.ORG

References to Accepted Names in Bold-Faced Print, to Synonyms in Upright Print, to Illustrations in Italics

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text

Load more

Index References to accepted names in bold-faced print, to synonyms in upright print, to illustrations in italics. A A. quaternata, 258 Annesorhiza, 101 Absolmsia, 333 A. sect. Tonduzia, 259 Anodendron, 302 Acanthopanax, 441 Alstonieae, 257 Anomalluma, 342 Acerates, 370 Alyxia, 276 Anomopanax, 84 Aciphylla, 95 A. concatenata, 276 Anomotassa, 381 Acokanthera, 280 Alyxieae, 274 Anthanotis, 370 Acomosperma, 392 Amalocalyx, 306 Anthocleista, 493 Acrocoryne, 382 Amarella, 488 Anthoclitandra, 264 Acronema, 96 Ambelania, 267 Anthriscus, 102 Actinolema, 92 Amblyopetalum, 386 A. caucalis, 102 A. macrolema, 92 Ammi, 98 A. caucalis var. caucalis, 102 Actinotus, 82 A. majus, 14 A. caucalis var. gymnocarpa, 102 Acustelma, 317 Ammodaucus, 99 A. kotschyi, 102 Adelostemma, 377 Ammoides, 99 A. sylvestris, 18, 102 Adelphacme, 520 Ammoselinum, 99 Antiostelma, 333 Adenium, 285 Ampelamus, 377 Antonia, 520 Adenolisianthus, 497 Amphidetes, 391 Antoniaceae, 511 Adenosciadium, 96 Amphineurion, 302 Antonieae, 520 Aegokeras, 96 Amphistelma, 380 Antoniinae, 520 Aegopodium, 96 Amphorella, 388 Apegia, 344 Aenigma, 397 Amsonia, 271 Aphanopleura, 102 Aethusa, 97 Amsonieae, 271 Aphanostelma, 386 Aframmi, 137, 158 Anagallidium, 489 Aphanostylis, 264 Afrocarum, 107 Anakasia, 436 Apiaceae, 9 Afroligusticum, 97 Anatropanthus, 329 Apiastrum, 103 Afrosciadium, 97 Ancylobothrys, 263 Apioideae, 95 Afrosison, 170 Andrewsia, 486 Apiopetalum, 82 Aganonerion, 305 Andriana, 99 A. glabratum, 83 Aganosma, 306 Anechites, 278 A. velutinum, 83 A. sect. Amphineurion, 302 Anemotrochus, 387 Apium, 103 Agasyllis, 97 Anethum, 99 Apocinae, 207 Agathotes, 489 Angadenia, 294 Apocynaceae, 207 Agrocharis, 97 Angelica, 100 Apocyneae, 301 Aidomene, 370 A. czernaevia, 18 Apocynoideae, 281 Alafia, 286 A. decurrens, 14 Apocynoids, 281 Albovia, 170 Anginon, 100 Apocynum, 304 Alepidea, 92 Angolluma, 349 Apodicarpum, 103 Aletes, 98 Angoseseli, 100 Apophragma, 472 Aliopsis, 488 Anidrum Apoxyanthera, 318 Allamanda, 277 Anidrum sect. Lipskya, 149 Apteranthes, 343 Allomarkgrafia, 295 Anisopoda, 101 Arafoe, 103 Allotoonia, 300 Anisopus, 329 Aralia, 432 Allowoodsonia, 290 Anisosciadium, 101 A. californica, 419 Alococarpum, 98 Anisotoma, 341 A. nudicaulis, 419 Aloitis, 488 Anisotomaria, 341 A. tibetana, 432 Alposelinum, 150 Anisotome, 101 Araliaceae, 413 Alstonia, 257 Anisotominae, 341 Aralidium, 552 # Springer International Publishing AG, part of Springer Nature 2018 557 J.W. Kadereit, V. Bittrich (eds.), Flowering Plants. Eudicots, The Families and Genera of Vascular Plants 15, https://doi.org/10.1007/978-3-319-93605-5 558 Index Aralidium, 552 (cont.) Azorella, 86 B. lophocarpum, 18 A. pinnatifidum, 553 Azorelloideae, 86 B. papillosum, 18, 19 Araujia, 384 B. rotundifolium, 15 Arctogentia, 488 B. sibiricum, 18 Arctopus, 93 B Bursaria, 544 Arcuatopterus, 103 Baeolepis, 314 Argelia, 375 Baharuia, 306 Argyronerium, 307 Bahiella, 300 C Aripuana, 496 Baissea, 308 Cabucala, 260 Arracacia, 104 Baisseeae, 307 Cachrys, 109 Artedia, 104 Ballyanthus, 346 Calathiana, 483 Arthrophyllum, 435 Barjonia, 381 Calathostelma, 381 Artia, 301 Baroniella, 311 Calciphila, 371 Asciadium, 104 Barrowia, 340 Callaeolepium, 391 Asclepiadaceae, 207 Bartonia, 486 Callichilia, 268 Asclepiadeae, 207, 354 Baseonema, 312 Calocrater, 269 Asclepiadinae, 370 Batesanthus, 312 Calolisianthus, 498 Asclepiadoideae, 324 Baynesia, 343 Calotropis, 371 Asclepias, 370 Beaumontia, 304 Calpicarpum, 259 Asclepiodella, 370 Belmontia, 473 Calyptranthera, 322 Asketanthera, 299 Bentleya, 546 Calyptrosciadium, 110 Aspidoglossum, 371 Berula, 107 Cameraria, 278 Aspidonepsis, 371 B. erecta, 108 Campelepis, 317 Aspidosperma, 256 Bidaria, 332 Campestigma, 330 A. excelsum, 257 Bifora, 107 Camptocarpus, 312 A. neblinae, 257 Bilacunaria, 108 Canaria, 181 A. pachypterum, 257 Billardiera, 545 Cannaboides, 110 Aspidospermateae, 255 Billburttia, 108 Canscora, 480 Astelma, 334 Biondia, 378 C. roxburghii, 476 Astephaninae, 369 Bisgoeppertia, 492 Canscorinae, 479 Astephanus, 369 Blaberopus, 257 Canscorinella, 480 Asteriscium, 86 Blackstonia, 476 Capnophyllum, 110 Asterostemma, 329 Bleekeria, 259 Caralluma, 344 Astomaea, 104 Blepharaden, 489 Carissa, 280 Astomatopsis, 105 Blepharanthera, 344 C. lanceolata, 281 Astrantia, 93 Blepharodon, 381 C. laxiflora, 281 A.major, 14 Blyttia, 378 C. ovata, 281 A. maxima, 18 Boerlagiodendron, 429 C. scabra, 281 A. pontica, 16 Bolax, 87 Carisseae, 280 A. trifida, 93 Bonannia, 108 Carlesia, 110 Astrodaucus, 105 Bonyunia, 520 Caropsis, 111 A. littoralis, 16, 18 B. superba, 512 Caroselinum, 123 Astropanax, 431 Borealluma, 343 Carpodinopsis, 274 Astrotricha, 428 Boucerosia, 343 Carpodinus, 264 Astydamia, 105 Bousigonia, 262 Carruthersia, 289 Athamanta, 105 Bowlesia, 87 Carum, 111 Atherandra, 311 B. palmata, 88 Caruncularia, 352 Atherolepis, 315 Brachyapium, 191 Carvalhoa, 270 Atherostemon, 311 Brachycodon, 496 Cascabela, 279 Atrema, 106 Brachylepis, 314 Catharanthus, 260 Atrostemma, 387 Brachyscias, 82 Cathetostemma, 330 Aulacospermum, 106 Brachystelma, 344 Caucalis, 111 A. anomalum, 14 Brachystelmaria, 344 C. platycarpos, 14 A. sect. Pseudotrachydium, 176 Brargentina, 388 Caudanthera, 344 Aulostephanus, 341 Brassaia, 436 Celiantha, 496 Auranticarpa, 545 Brassaiopsis, 440 Cenolophium, 111 Australluma, 343 Bruceholstia, 388 Centaurella, 486 Austrochthamalia, 387 Bubon, 109 Centaurium, 477 Austropeucedanum, 106 Buckollia, 312 C. beyrichii, 476 Autumnalia, 106 Buniella, 127 C. sect. Spicaria, 479 A. innopinata, 107 Bunium, 109 Centella, 83 Azilia, 107 Bupleurum, 109 Cephalaralia, 429 Index 559 Cephalopodum, 112 Clitandra, 263 Cyclocotyla, 262 Ceramanthus, 385 C. sect. Chamaeclitandra, 264 Cyclodon, 389 Cerbera, 279 Clitandropsis, 273 Cyclorhiza, 119 C. laeta, 279 Cnidiocarpa, 115 Cyclospermum, 119 Cerberiopsis, 280 Cnidium, 115 Cylindrilluma, 348 Cerberoideae, 253 C. monnieri, 14 Cylindropsis, 262 Ceropegia, 344 Coaxana, 115 Cylixylon, 315 C. zambesiaca, 345 Coelostelma, 389 Cymbocarpum, 119 Ceropegieae, 336 Coelostyleae, 522 Cymopterus, 120 Cervaria, 112 Coelostylis, 522 Cynanchinae, 377 Chabraea, 123 Comastoma, 487 Cynanchum, 213, 377 Chaerefolium, 102 Condylocarpon, 275 C. sect. Formosum, 380 Chaerophyllopsis, 112 Congolanthus, 489 C. sect. Microphyllum, 380 Chaerophyllum, 112 Conioselinum, 116 Cynapium, 120 C. aureum, 16, 18 Conium, 116 Cynoctonum, 521 C. prescottii, 14 Conomitra, 340 Cynorhiza, 120 Chaetosciadium, 113 Conopodium, 116 Cynosciadium, 121 C. trichospermum, 18 Cordylogyne, 372 Cyprinia, 317 Chamaeclitandra, 264 Coriandropsis, 116 Cyrtophyllum, 492 Chamaele, 96 Coriandrum, 116 Chamaesciadium, 113 Coristospermum, 117 Chamaesium, 113 Cornacchinia, 314 D Chamarea, 113 Corollonema, 386 Dactylostelma, 386 Changium, 114 Cortia, 117 Dahliaphyllum, 121 Chavannesia, 305 Cortiella, 117 Dalzielia, 334 Cheiranthera, 546 Cosmostigma, 330 Dasispermum, 121 Cheirodendron, 430 Costantina, 333 Dasystephana, 483 Chelidospermum, 545 Cotopaxia, 117 Daucosma, 121 Chelonanthus, 498 Cotylanthera, 474 Daucus, 122 C. alatus, 494 Coulterophytum, 118 Decabelone, 352 Chengiopanax, 439 Couma, 266 Decalepis, 314 Chilocarpus, 275 Couthovia, 523 Decanema, 377 Chionogentias, 488 Coutoubea, 481 Decanemopsis, 377 Chironia, 477 C. spicata, 476 Decodontia, 347 C. laxiflora, 476 Coutoubeinae, 481 Decostea, 507 Chironieae, 476 Coxella, 95 Deianira, 482 Chironiinae, 476 Cracosna, 480 Delarbrea, 530 Chlaenosciadium, 83 Craspidospermum, 272 D. montana ssp. Chlora, 476 C. verticillatum, 272 montana, 531 Chlorocodon, 316 Crawfurdia, 484 Delphyodon, 300 Chlorocyathus, 313 Crenosciadium, 118 Demavendia, 122 Chloropetalum, 388 Crenulluma, 345 Dendropanax, 439 Chondrophylla, 483 Crepinella, 436 D. fluminensis, 440 Chonemorpha, 305 Crioceras, 269 Desmidorchis, 345 Chorisepalum, 495 Cristobalia, 389 Dethawia, 122 Choristigma, 385 Crithmum, 118 Deverra, 123 Choritaenia, 114 Crossopetalum, 485 Dewevrella, 308 Christya, 286 Cryptolepis, 313 Dicarpophora, 380 Chthamalia, 388 C. macrophylla, 313 Dicerolepis, 315 Chuanminshen, 114 Cryptolluma, 344 Dichaelia, 344 Chunechites, 305 Cryptostegia, 314 Dichoropetalum, 123 Chymocormus, 325 Cryptotaenia, 118 Dichosciadium, 87 Chymsydia, 114 Cuminum, 119 Dickinsia, 87 Cibirhiza, 325 Cuphocarpus, 435 Dictyanthus, 389 Cicendia, 477 Curroria, 313 Dictyophleba, 263 Cicuta, 114 Curtia, 472 Dicyclophora, 123 Ciminalis, 483 C. obtusifolia, 472 Didiscus, 427 Cionura, 330 C. tenuifolia, 472 Didymopanax, 436 Citriobatus, 543 Cussonia, 430 Dimorphosciadium, 123 Cleghornia, 304 Cyathoselinum, 119 Dipladenia, 296 Clemensia, 333 Cyathostelma, 380 Diplaspis, 88 Clemensiella, 333 Cycladenia, 293 Diplocyatha, 349 560 Index Diplolepinae, 379 Emplectanthus, 341 Fergania, 130 Diplolepis, 379 Enantiophylla, 127 Fernaldia, 300 Diplolophium, 124 Endressia, 127 Ferula, 130 Diplorhynchus, 271 Enicostema, 491 F. rutbaensis, 16 Diplostigma, 378 E. verticillatum, 490 Ferulago, 130 Diplotaenia, 124 Ephippiocarpa, 268 Ferulopsis, 131 Diposis, 88 Epigynum, 307 Fimbristemma, 390 Discalyxia, 276 Epikeros, 100 Finlaysonia, 315 Dischidanthus, 334 Epistemma, 314 Fischeria, 390 Dischidia, 330 Eremocharis, 89 Flanagania, 377 Dischidiopsis, 330 Eremodaucus, 127 Fockea, 325 Distichoselinum, 194 E. lehmannii, 128 F. edulis, 326 Ditassa, 381 Eremopanax, 435 Fockeeae, 325 Dittoceras, 339 Ergocarpon, 128 Foeniculum, 131 Dizygotheca, 434 Ericoila, 483 Folotsia, 377 Djaloniella, 490 Erigenia, 128 Fontellaea, 386 Dolichopetalum, 331 Eriopetalum, 344 Formosia, 302 Dolichostegia, 330 Eriosynaphe, 129 Formosum, 380 Dolpojestella, 113 Eryngium, 94 Forsteronia, 296 Domeykoa, 89 E. bungei, 94
Recommended publications
  • Flowering Plants Eudicots Apiales, Gentianales (Except Rubiaceae)

    Flowering Plants Eudicots Apiales, Gentianales (Except Rubiaceae)

    Edited by K. Kubitzki Volume XV Flowering Plants Eudicots Apiales, Gentianales (except Rubiaceae) Joachim W. Kadereit · Volker Bittrich (Eds.) THE FAMILIES AND GENERA OF VASCULAR PLANTS Edited by K. Kubitzki For further volumes see list at the end of the book and: http://www.springer.com/series/1306 The Families and Genera of Vascular Plants Edited by K. Kubitzki Flowering Plants Á Eudicots XV Apiales, Gentianales (except Rubiaceae) Volume Editors: Joachim W. Kadereit • Volker Bittrich With 85 Figures Editors Joachim W. Kadereit Volker Bittrich Johannes Gutenberg Campinas Universita¨t Mainz Brazil Mainz Germany Series Editor Prof. Dr. Klaus Kubitzki Universita¨t Hamburg Biozentrum Klein-Flottbek und Botanischer Garten 22609 Hamburg Germany The Families and Genera of Vascular Plants ISBN 978-3-319-93604-8 ISBN 978-3-319-93605-5 (eBook) https://doi.org/10.1007/978-3-319-93605-5 Library of Congress Control Number: 2018961008 # Springer International Publishing AG, part of Springer Nature 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.
  • Chapter 2.Indd

    Chapter 2.Indd

    Gardens’ Bulletin Singapore 69(1): 33–65. 2017 33 doi: 10.3850/S2010098116000039 Index of names and types of Hoya (Apocynaceae: Asclepiadoideae) of Borneo M. Rodda Herbarium, Singapore Botanic Gardens, National Parks Board, 1 Cluny Road, Singapore 259569 [email protected] ABSTRACT. Types of all Hoya species occurring in Borneo and their synonyms are indicated and clarified. Forty-six lectotypes, nine neotypes and five epitypes are designated. Keywords. Brunei, epitype, holotype, Kalimantan, lectotype, neotype, Sabah, Sarawak Introduction The present paper is a precursor to a revision of Hoya R.Br. of Borneo. Its aim is to list all Hoya taxa occurring on the island of Borneo and their synonyms, clarify and standardize type citation, select lectotypes, epitypes and neotypes when necessary and provide an extensive list of isotypes and syntypes. The earliest description of a Hoya species that occurs in Borneo, H. multiflora Blume, was described by the German born Dutch botanist Carl Ludwig Blume in 1823, based, however, on Javanese materials. The first Hoya species based on a Bornean collection, H. imperialis Lindl., was published by Lindley (1846). Later, in 1880, Bentham published a peculiar leafless species with long photosynthetic peduncles endemic to Borneo, Astrostemma spartioides Benth. (now Hoya spartioides (Benth.) Kloppenb.). Until 1921 only nine Hoya species where known to occur in Borneo (Merrill, 1921). Nutt (2001) listed 21 species in an unpublished checklist. Lamb et al. (2014) estimated 60–70 species for Sabah alone. In the past 20 years almost 40 taxa (species and subspecies) of Hoya from Borneo have been described, mostly by Ted Green and Dale Kloppenburg (USA).
  • Ethnobotanical Study on Wild Edible Plants Used by Three Trans-Boundary Ethnic Groups in Jiangcheng County, Pu’Er, Southwest China

    Ethnobotanical Study on Wild Edible Plants Used by Three Trans-Boundary Ethnic Groups in Jiangcheng County, Pu’Er, Southwest China

    Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Yilin Cao Agriculture Service Center, Zhengdong Township, Pu'er City, Yunnan China ren li ( [email protected] ) Xishuangbanna Tropical Botanical Garden https://orcid.org/0000-0003-0810-0359 Shishun Zhou Shoutheast Asia Biodiversity Research Institute, Chinese Academy of Sciences & Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Liang Song Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences & Center for Intergrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Ruichang Quan Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences & Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Huabin Hu CAS Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Research Keywords: wild edible plants, trans-boundary ethnic groups, traditional knowledge, conservation and sustainable use, Jiangcheng County Posted Date: September 29th, 2020 DOI: https://doi.org/10.21203/rs.3.rs-40805/v2 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Version of Record: A version of this preprint was published on October 27th, 2020. See the published version at https://doi.org/10.1186/s13002-020-00420-1. Page 1/35 Abstract Background: Dai, Hani, and Yao people, in the trans-boundary region between China, Laos, and Vietnam, have gathered plentiful traditional knowledge about wild edible plants during their long history of understanding and using natural resources. The ecologically rich environment and the multi-ethnic integration provide a valuable foundation and driving force for high biodiversity and cultural diversity in this region.
  • Check List of Wild Angiosperms of Bhagwan Mahavir (Molem

    Check List of Wild Angiosperms of Bhagwan Mahavir (Molem

    Check List 9(2): 186–207, 2013 © 2013 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution Check List of Wild Angiosperms of Bhagwan Mahavir PECIES S OF Mandar Nilkanth Datar 1* and P. Lakshminarasimhan 2 ISTS L (Molem) National Park, Goa, India *1 CorrespondingAgharkar Research author Institute, E-mail: G. [email protected] G. Agarkar Road, Pune - 411 004. Maharashtra, India. 2 Central National Herbarium, Botanical Survey of India, P. O. Botanic Garden, Howrah - 711 103. West Bengal, India. Abstract: Bhagwan Mahavir (Molem) National Park, the only National park in Goa, was evaluated for it’s diversity of Angiosperms. A total number of 721 wild species belonging to 119 families were documented from this protected area of which 126 are endemics. A checklist of these species is provided here. Introduction in the National Park are Laterite and Deccan trap Basalt Protected areas are most important in many ways for (Naik, 1995). Soil in most places of the National Park area conservation of biodiversity. Worldwide there are 102,102 is laterite of high and low level type formed by natural Protected Areas covering 18.8 million km2 metamorphosis and degradation of undulation rocks. network of 660 Protected Areas including 99 National Minerals like bauxite, iron and manganese are obtained Parks, 514 Wildlife Sanctuaries, 43 Conservation. India Reserves has a from these soils. The general climate of the area is tropical and 4 Community Reserves covering a total of 158,373 km2 with high percentage of humidity throughout the year.
  • FINAL REPORT PSRA Vegetation Monitoring 2005-2006 PC P502173

    FINAL REPORT PSRA Vegetation Monitoring 2005-2006 PC P502173

    Rare Plants and Their Locations at Picayune Strand Restoration Area: Task 4a FINAL REPORT PSRA Vegetation Monitoring 2005-2006 PC P502173 Steven W. Woodmansee and Michael J. Barry [email protected] December 20, 2006 Submitted by The Institute for Regional Conservation 22601 S.W. 152 Avenue, Miami, Florida 33170 George D. Gann, Executive Director Submitted to Mike Duever, Ph.D. Senior Environmental Scientist South Florida Water Management District Fort Myers Service Center 2301 McGregor Blvd. Fort Myers, Florida 33901 Table of Contents Introduction 03 Methods 03 Results and Discussion 05 Acknowledgements 38 Citations 39 Tables: Table 1: Rare plants recorded in the vicinity of the Vegetation Monitoring Transects 05 Table 2: The Vascular Plants of Picayune Strand State Forest 24 Figures: Figure 1: Picayune Strand Restoration Area 04 Figure 2: PSRA Rare Plants: Florida Panther NWR East 13 Figure 3: PSRA Rare Plants: Florida Panther NWR West 14 Figure 4: PSRA Rare Plants: PSSF Northeast 15 Figure 5: PSRA Rare Plants: PSSF Northwest 16 Figure 6: PSRA Rare Plants: FSPSP West 17 Figure 7: PSRA Rare Plants: PSSF Southeast 18 Figure 8: PSRA Rare Plants: PSSF Southwest 19 Figure 9: PSRA Rare Plants: FSPSP East 20 Figure 10: PSRA Rare Plants: TTINWR 21 Cover Photo: Bulbous adder’s tongue (Ophioglossum crotalophoroides), a species newly recorded for Collier County, and ranked as Critically Imperiled in South Florida by The Institute for Regional Conservation taken by the primary author. 2 Introduction The South Florida Water Management District (SFWMD) plans on restoring the hydrology at Picayune Strand Restoration Area (PSRA) see Figure 1.
  • Progress on Southeast Asia's Flora Projects

    Progress on Southeast Asia's Flora Projects

    Gardens' Bulletin Singapore 71 (2): 267–319. 2019 267 doi: 10.26492/gbs71(2).2019-02 Progress on Southeast Asia’s Flora projects D.J. Middleton1, K. Armstrong2, Y. Baba3, H. Balslev4, K. Chayamarit5, R.C.K. Chung6, B.J. Conn7, E.S. Fernando8, K. Fujikawa9, R. Kiew6, H.T. Luu10, Mu Mu Aung11, M.F. Newman12, S. Tagane13, N. Tanaka14, D.C. Thomas1, T.B. Tran15, T.M.A. Utteridge16, P.C. van Welzen17, D. Widyatmoko18, T. Yahara14 & K.M. Wong1 1Singapore Botanic Gardens, National Parks Board, 1 Cluny Road, 259569 Singapore [email protected] 2New York Botanical Garden, 2900 Southern Boulevard, Bronx, New York, 10458, USA 3Auckland War Memorial Museum Tāmaki Paenga Hira, Private Bag 92018, Auckland 1142, New Zealand 4Ecoinformatics and Biodiversity, Department of Bioscience, Aarhus University Building 1540, Ny Munkegade 114, Aarhus C DK 8000, Denmark 5The Forest Herbarium, National Park, Wildlife and Plant Conservation Department, 61 Phahonyothin Rd., Chatuchak, Bangkok 10900, Thailand 6Herbarium, Forest Research Institute Malaysia, Kepong, Selangor 52109, Malaysia 7School of Life and Environmental Sciences, University of Sydney, NSW 2006, Australia 8Department of Forest Biological Sciences, College of Forestry & Natural Resources, University of the Philippines - Los Baños, College, 4031 Laguna, Philippines 9Kochi Prefectural Makino Botanical Garden, 4200-6 Godaisan, Kochi, 7818125, Japan 10Southern Institute of Ecology, Vietnam Academy of Science and Technology, 01 Mac Dinh Chi Street, District 1, Ho Chi Minh City, Vietnam 11Forest
  • Epilist 1.0: a Global Checklist of Vascular Epiphytes

    Epilist 1.0: a Global Checklist of Vascular Epiphytes

    Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2021 EpiList 1.0: a global checklist of vascular epiphytes Zotz, Gerhard ; Weigelt, Patrick ; Kessler, Michael ; Kreft, Holger ; Taylor, Amanda Abstract: Epiphytes make up roughly 10% of all vascular plant species globally and play important functional roles, especially in tropical forests. However, to date, there is no comprehensive list of vas- cular epiphyte species. Here, we present EpiList 1.0, the first global list of vascular epiphytes based on standardized definitions and taxonomy. We include obligate epiphytes, facultative epiphytes, and hemiepiphytes, as the latter share the vulnerable epiphytic stage as juveniles. Based on 978 references, the checklist includes >31,000 species of 79 plant families. Species names were standardized against World Flora Online for seed plants and against the World Ferns database for lycophytes and ferns. In cases of species missing from these databases, we used other databases (mostly World Checklist of Selected Plant Families). For all species, author names and IDs for World Flora Online entries are provided to facilitate the alignment with other plant databases, and to avoid ambiguities. EpiList 1.0 will be a rich source for synthetic studies in ecology, biogeography, and evolutionary biology as it offers, for the first time, a species‐level overview over all currently known vascular epiphytes. At the same time, the list represents work in progress: species descriptions of epiphytic taxa are ongoing and published life form information in floristic inventories and trait and distribution databases is often incomplete and sometimes evenwrong.
  • Apocynaceae-Apocynoideae)

    Apocynaceae-Apocynoideae)

    THE NERIEAE (APOCYNACEAE-APOCYNOIDEAE) A. J. M. LEEUWENBERG1 ABSTRACT The genera of tribe Nerieae of Apocynaceae are surveyed here and the relationships of the tribe within the family are evaluated. Recent monographic work in the tribe enabled the author to update taxonomie approaches since Pichon (1950) made the last survey. Original observations on the pollen morphology ofth egener a by S.Nilsson ,Swedis h Natural History Museum, Stockholm, are appended to this paper. RÉSUMÉ L'auteur étudie lesgenre s de la tribu desNeriea e desApocynacée s et évalue lesrelation s del a tribu au sein de la famille. Un travail monographique récent sur la tribu a permit à l'auteur de mettre à jour lesapproche s taxonomiques depuis la dernière étude de Pichon (1950). Lesobservation s inédites par S. Nilsson du Muséum d'Histoire Naturelle Suédois à Stockholm sur la morphologie des pollens des genres sontjointe s à cet article. The Apocynaceae have long been divided into it to generic rank and in his arrangement includ­ two subfamilies, Plumerioideae and Apocynoi- ed Aganosma in the Echitinae. Further, because deae (Echitoideae). Pichon (1947) added a third, of its conspicuous resemblance to Beaumontia, the Cerberioideae, a segregate of Plumerioi­ it may well be that Amalocalyx (Echiteae— deae—a situation which I have provisionally ac­ Amalocalycinae, according to Pichon) ought to cepted. These subfamilies were in turn divided be moved to the Nerieae. into tribes and subtribes. Comparative studies Pichon's system is artificial, because he used have shown that the subdivision of the Plume­ the shape and the indumentum of the area where rioideae is much more natural than that of the the connectives cohere with the head of the pistil Apocynoideae.
  • Phylogeny and Systematics of the Rauvolfioideae

    Phylogeny and Systematics of the Rauvolfioideae

    PHYLOGENY AND SYSTEMATICS Andre´ O. Simo˜es,2 Tatyana Livshultz,3 Elena OF THE RAUVOLFIOIDEAE Conti,2 and Mary E. Endress2 (APOCYNACEAE) BASED ON MOLECULAR AND MORPHOLOGICAL EVIDENCE1 ABSTRACT To elucidate deeper relationships within Rauvolfioideae (Apocynaceae), a phylogenetic analysis was conducted using sequences from five DNA regions of the chloroplast genome (matK, rbcL, rpl16 intron, rps16 intron, and 39 trnK intron), as well as morphology. Bayesian and parsimony analyses were performed on sequences from 50 taxa of Rauvolfioideae and 16 taxa from Apocynoideae. Neither subfamily is monophyletic, Rauvolfioideae because it is a grade and Apocynoideae because the subfamilies Periplocoideae, Secamonoideae, and Asclepiadoideae nest within it. In addition, three of the nine currently recognized tribes of Rauvolfioideae (Alstonieae, Melodineae, and Vinceae) are polyphyletic. We discuss morphological characters and identify pervasive homoplasy, particularly among fruit and seed characters previously used to delimit tribes in Rauvolfioideae, as the major source of incongruence between traditional classifications and our phylogenetic results. Based on our phylogeny, simple style-heads, syncarpous ovaries, indehiscent fruits, and winged seeds have evolved in parallel numerous times. A revised classification is offered for the subfamily, its tribes, and inclusive genera. Key words: Apocynaceae, classification, homoplasy, molecular phylogenetics, morphology, Rauvolfioideae, system- atics. During the past decade, phylogenetic studies, (Civeyrel et al., 1998; Civeyrel & Rowe, 2001; Liede especially those employing molecular data, have et al., 2002a, b; Rapini et al., 2003; Meve & Liede, significantly improved our understanding of higher- 2002, 2004; Verhoeven et al., 2003; Liede & Meve, level relationships within Apocynaceae s.l., leading to 2004; Liede-Schumann et al., 2005). the recognition of this family as a strongly supported Despite significant insights gained from studies clade composed of the traditional Apocynaceae s.
  • PLANT SCIENCE Bulletin Fall 2013 Volume 59 Number 3

    PLANT SCIENCE Bulletin Fall 2013 Volume 59 Number 3

    PLANT SCIENCE Bulletin Fall 2013 Volume 59 Number 3 Botany in Action - in New Orleans! In This Issue.............. More BSA awards announced at PlantingScience mentors Botany 2013!.....p. 146 Botany 2013.....p. 80 make a difference.....p. 90 From the Editor PLANT SCIENCE BULLETIN The good news these days is about resources. There is so much information readily available on the internet Editorial Committee that one hardly needs to leave the office to work on a Volume 59 literature review or gather information for a lecture. The first step—Google it! The bad news these days is Elizabeth Schussler about resources. There is so much information readily (2013) available on the internet that one could spend hours Department of Ecology & sorting through possible sites to find the information Evolutionary Biology you want. What we need is a resource that has done University of Tennessee the dirty work of searching what is available and evalu- Knoxville, TN 37996-1610 ating its usefulness. That resource has been provided [email protected] for botanical and lichenological systematic research by Morgan Gostel, Manuela Dal-Forno, and Andrea Weeks in this issue. This is also a great resource to use for teaching images. Christopher Martine (2014) In our other feature article, Melanie Link-Pérez and Department of Biology Elizabeth Schussler demonstrate that resources, by Bucknell University themselves, are not enough to support grade-school Lewisburg, PA 17837 teachers in their efforts to introduce plant science to [email protected] students. At this age the kids love plants and so do the teachers, and the teachers are anxious to find and use resources to help them incorporate plants into the curriculum.
  • Floral Glands in Asclepiads: Structure, Diversity and Evolution

    Floral Glands in Asclepiads: Structure, Diversity and Evolution

    Acta Botanica Brasilica - 31(3): 477-502. July-September 2017. doi: 10.1590/0102-33062016abb0432 Review Floral glands in asclepiads: structure, diversity and evolution Diego Demarco1 Received: December 7, 2016 Accepted: February 24, 2017 . ABSTRACT Species of Apocynaceae stand out among angiosperms in having very complex fl owers, especially those of asclepiads, which belong to the most derived subfamily (Asclepiadoideae). Th ese fl owers are known to represent the highest degree of fl oral synorganization of the eudicots, and are comparable only to orchids. Th is morphological complexity may also be understood by observing their glands. Asclepiads have several protective and nuptial secretory structures. Th eir highly specifi c and specialized pollination systems are associated with the great diversity of glands found in their fl owers. Th is review gathers data regarding all types of fl oral glands described for asclepiads and adds three new types (glandular trichome, secretory idioblast and obturator), for a total of 13 types of glands. Some of the species reported here may have dozens of glands of up to 11 types on a single fl ower, corresponding to the largest diversity of glands recorded to date for a single structure. Keywords: anatomy, Apocynaceae, Asclepiadoideae, diversity, evolution, fl ower, secretory structures considering its most derived subfamily Asclepiadoideae. Introduction Th e close relationship between the former families Apocynaceae and Asclepiadaceae has always been recognized Apocynaceae is an extremely diverse family in since its establishment as “Apocineae” by Jussieu (1789). morphological terms, represented by trees, shrubs, herbs and climbers, with single leaves usually opposite, rarely Although Brown (1810) divided it into two families and alternate or whorled, with stipules modifi ed in colleters in this separation had been maintained in the subsequent several species (Endress & Bruyns 2000; Capelli et al.
  • Ethnobotanical Knowledge of the Kuy and Khmer People in Prey Lang, Cambodia

    Ethnobotanical Knowledge of the Kuy and Khmer People in Prey Lang, Cambodia

    Ethnobotanical knowledge of the Kuy and Khmer people in Prey Lang, Cambodia Turreira Garcia, Nerea; Argyriou, Dimitrios; Chhang, Phourin; Srisanga, Prachaya; Theilade, Ida Published in: Cambodian Journal of Natural History Publication date: 2017 Document version Publisher's PDF, also known as Version of record Citation for published version (APA): Turreira Garcia, N., Argyriou, D., Chhang, P., Srisanga, P., & Theilade, I. (2017). Ethnobotanical knowledge of the Kuy and Khmer people in Prey Lang, Cambodia. Cambodian Journal of Natural History, 2017(1), 76-101. http://www.fauna-flora.org/wp-content/uploads/CJNH-2017-June.pdf Download date: 26. Sep. 2021 76 N. Turreira-García et al. Ethnobotanical knowledge of the Kuy and Khmer people in Prey Lang, Cambodia Nerea TURREIRA-GARCIA1,*, Dimitrios ARGYRIOU1, CHHANG Phourin2, Prachaya SRISANGA3 & Ida THEILADE1,* 1 Department of Food and Resource Economics, University of Copenhagen, Rolighedsvej 25, 1958 Frederiksberg, Denmark. 2 Forest and Wildlife Research Institute, Forestry Administration, Hanoi Street 1019, Phum Rongchak, Sankat Phnom Penh Tmei, Khan Sen Sok, Phnom Penh, Cambodia. 3 Herbarium, Queen Sirikit Botanic Garden, P.O. Box 7, Maerim, Chiang Mai 50180, Thailand. * Corresponding authors. Email [email protected], [email protected] Paper submitted 30 September 2016, revised manuscript accepted 11 April 2017. ɊɮɍɅʂɋɑɳȶɆſ ȹɅƺɁɩɳȼˊɊNJȴɁɩȷ Ʌɩȶ ɑɒȴɊɅɿɴȼɍɈɫȶɴɇơȲɳɍˊɵƙɈɳȺˊƙɁȪɎLJɅɳȴȼɫȶǃNjɅȷɸɳɀɹȼɫȶɈɩɳɑɑ ɳɍˊɄɅDžɅɄɊƗƺɁɩɳǷȹɭɸ ɎȻɁɩ ɸɆɅɽɈɯȲɳȴɌɑɽɳǷʆ ɳDŽɹƺnjɻ ȶǁ ƳɌȳɮȷɆɌǒɩ Ə ɅLJɅɆɅƏɋȲƙɊɩɁɄɅDžɅɄɊƗƺɁɩɴȼɍDžƚ ɆɽNjɅ