Incl. Basio- Implied That Lectotypification Is Sub-Regional Flora Subsequ

Total Page:16

File Type:pdf, Size:1020Kb

Incl. Basio- Implied That Lectotypification Is Sub-Regional Flora Subsequ BLUMEA Supplement 8 (1995) 1-161 Checklist of the Araceae of Malesia, Australia, and the tropical western Pacific region A. Hay P.C. Boyce W.L.A. Hetterscheid N. Jacobsen J. Murata and J. Bogner Summary A checklist of Malesian, Australian and Tropical Western Pacific Araceae is provided, giving generic names, specific and infraspecific binomials and trinomials (generally not below the level of variety), and lower and lower basionyms, synonyms at generic levels, protologues at specific levels, type specimens or equivalent elements and their locations, distribution of accepted taxa and status (native, status introduced or unknown), coded revision of accepted genera and nomenclatural notes where nec- essary. In total 1,437names are listed. Thirty-six genera are currently accepted. Introduction to The checklist is a precursor revisions of Australian, Tropical Western Pacific and Malesian Araceae, to the Flora of Australia, Flora Malesiana and sub-regional flora accounts and to subsequent monographic work which may eventuate. As such, it is intended be aid work in is to an to progress. It arranged alphabetically by genus and species. Accepted names (i.e., valid names accepted by the most recent reviser and those in published since) are bold print; synonyms and invalidor illegitimate names are in italics. Nomina nuda, in particular those from the horticultural literature, are generally not included. followed their when entire Accepted generic names are by synonyms (but only an generic concept has been subsumed - no partial generic synonyms are included). Then = there is a coded indicationof revision status: A recently revised or currently under active revision at an advanced stage, B = partially revised recently, C = not revised for 40 years or more. Accepted specific and lower ranking names are followed by synonyms (incl. basio- - of then nym): then a reference being the earliest known valid publication the name; the - than element is is that is type where more one cited, it implied lectotypification 1 1 Royal Botanic Gardens Sydney, Mrs Macquarie's Road, Sydney NSW 2000, Australia. 21 Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, United Kingdom. 3 ) Chrysantenstraat 28, 1214 BM Hilversum, The Netherlands. 41 Institut for Botanik, Dendrologi og Forstgenetik, Den Kgl. Veteriner- og Landbohpjskole, Ro- lighedsvej 23, DK-1958 Frederiksberg C, Denmark. 51 Botanical Gardens Nikko, Faculty of Science, University ofTokyo, 1842 Hanaishi-cho, Nikko, Tochigi Pref., Japan. 6 ) Menzinger StraBe 63, D-80638 Munchen, Germany. 2 BLUMEA Supplement 8 (1995) required; material has not necessarily been seen by us but is presumed to be extant unless otherwise indicated [significant Araceae material at B survived World War II (Sleumer, Kew Bull. 1949: 172)]; locations of types are indicated by standard her- barium acronyms - they should not be taken as necessarily the only location(s) of a given collection; next, distributionis coded: AUSTRAL = Australia and associated small islands, BORBRUN = Brunei, BOR1ND = Kalimantan, BORSABAH = Sabah, = BORSAR = Sarawak, CELEBES = Sulawesi and associated islands, JAVA Java and associated islands, LSI = Lesser Sunda Islands, MALPEN = Peninsular Malaysia, of MOLUCCAS = Halmaheraand other islands the Moluccas, NGIND = Irian Jaya or West New Guinea and associated islands, NGPNG = Papua New Guinea or East New Guinea plus the Bismarck Archipelago and other associated islands but not Bougain- ville, PACIFIC = the island groups ofPolynesia, Micronesia and Melanesia excluding New Guinea, PHILIP = the Philippine islands, SINGAPORE = Singapore, SUMATRA = Sumatra and associated islands, OUTSIDE = elsewhere; the letters I, N or U between brackets following the distribution code signify, respectively, introduced or native to the area, or status unknown. Entries for include and in entries for synonyms protologue type as accepted names, but no data for distribution. Entries for basionyms include only the protologues where of the will be found they are basionyms accepted names (where types cited). Types of synonyms that have basionyms are to be found cited under those basio- nyms. Misapplications of names are not dealt with. Unpublished new species are not in- cluded unless in at the timeof this list. i.e. auto- they are press compiling 'Typical', nymous, varieties are included where one or more segregate variety(ies) is/are ac- avoid varieties cepted. To duplication, autonymous are not listed separately from their species. It should be understood that they are validated at the time of valid pub- lication of first of the segregate and not at the time first publication of the species (ICBN Art. 26.2). Authors checklists - supplied for the following genera Bogner & Boyce: Aridarum, Bucephalandra, Heteroaridarum, Hottarum, Phymatarum, Piptospatha. - Boyce: Amydrium, Epipremnum (W Malesia), Hapaline, Rhaphidophora (W Malesia), Scin- dapsus (W Malesia). - Hay: Aglaodorum, Aglaonema, Alocasia, Anadendrum, Colocasia, Cyrtosperma, Epipremnum (not W Malesia), Furtadoa, Gymnostachys, Holochlamys, Homalomena, Lasia, Lazarum, Nephthytis, Pedicellarum, Pistia, Podolasia, Pothoidium, Pothos, Remusatia, Rhaphidophora (not W Malesia), Schis- matoglottis, Scindapsus (not W Malesia), Spathiphyllum, Typhonium (not W Male- - sia). - Hetterscheid: Amorphophallus. - Jacobsen: Cryptocoryne. Murata: Arisaema, Typhonium (W Malesia). Checklist of Malesian, Australian, and tropical western Pacific Araceae 3 Checklist AGLAODORUM Schott Revision status - C Aglaodorum griffithii (Schott) Schott Syn.: Aglaonema griffithii Schott, Aglaonemapalustre Teijsm. & Binn. Ref.: Gen. Aroid. (1858) t. 58 Type: Griffith (K) Distr.: BORSAR (N), MALPEN (N), SUMATRA (N) AGLAONEMA Schott Revision - A: Nicolson, 1969. revision status D.H. A of the genus Aglaonema (Araceae). Smithsonian Contr. Bot. 1: 1-69. Aglaonema alpinum Elmer = Aglaonema simplex Blume Ref.: Leafl.Philipp. Bot. 10 (1938) 3611 Type: Elmer 16520 (BO, CAL, GH, NY) Note: invalid (no Latin). Aglaonema angustifolium N.E.Br. = Aglaonema simplex Blume Ref.: Kew Bull. (1895) 18 Type: N.E. Brown s.n. (K) undulatumRidl. = Blume Aglaonema angustifolium var. Aglaonema simplex Ref.: MaterialsFl. Mai. Pen. 1 (1907) 21 Note: nom. superfl. pro var. typ. Aglaonema borneense Engl. = Aglaonema simplex Blume Ref.: Pflanzenr. 64 (IV.23Dc) (1915) 22 Type: Engler s.n. (B) Aglaonema brevivaginatum Alderw. = Aglaonema simplex Blume Ref.: Bull. Jard. Bot. Buitenzorg 111, 4 (1922) 324 Type: Bunnemeijer 7044(80, L) Aglaonema commutatumSchott var. commutatum Syn.: Aglaonema marantifolium var. commutatum (Schott) Engl. Ref.: Syn. Aroid. (1856) 123 Type: drawing, Schott Aroideae No. 38 (W) Distr.: CELEBES (N), PHILIP (N) Note: varieties. The natural distribution of the is unknown. The see type variety species is widely naturalised, as are the varieties. Several cultivars are recog- nised in Nicolson, Smithsonian Contrib. Bot. 1 (1969) 52. The species is highly variable and the botanical significance of the varieties that Nicolson recognised is not certain. 4 BLUMEA Supplement 8 (1995) Aglaonema commutatum var. elegans (Engl.) Nicolson Syn.: Aglaonema elegans Engl. Ref.: Baileya 15 (1967) 125 Type: Pflanzenr. 64 (IV.23Dc) (1915) fig. 11 Distr.: PHILIP (N) Aglaonema commutatum var. maculatum (Elook. f.) Nicolson maculatum f. Syn.: Aglaonema marantifolium var. Hook. Ref.: Baileya 15 (1967) 125 Type: Chelsea, Royal Exotic Nursery (no collector cited) (K) Distr.: PHILIP (N) Aglaonema commutatum var. robustum (Alderw.) Nicolson Syn.: Aglaonema robustum Alderw. Ref.: Baileya 15 (1967) 125 Type: van Alderwerelt van Rosenburgh 358 (BO) Distr.: JAVA (?I) cultivated Note: based on material at Bogor of unknown origin. Aglaonema commutatum var. warburgii (Engl.) Nicolson Syn.: Aglaonema warburgii Engl. Ref.: Smithsonian Contrib. Bot. 1 (1969) 50 Type: Warburg s.n. (B) Distr.: CELEBES (N) Aglaonema cordifolium Engl Ref.: Pflanzenr. 64 (IV.23Dc) (1915) 29 Type: Warburg 14604 (B) Distr.: PHILIP (N) Aglaonema costatum N.E. Br. Syn: Aglaonema costatum var. foxii Engl., Aglaonema costatum var. maculatum Engl. Ref.: 426 Gard. Chron. ser. 3, 11 (1892) Type: N.E.Brown s.n. (K) Distr.: MALPEN (N), OUTSIDE (I, N) Note: Nicolson recognises a number of forms mostly originating outside Malesia (see Smithsonian Contrib. Bot. 1 (1969) 23). Aglaonema costatum var. foxii Engl. = Aglaonema costatum N.E. Br. Ref.: Pflanzenr. 64 (IV.23Dc) (1915) 17 Type: Curtis s.n. (7SING) Note: a dubious taxon with errors in the citation of the type locality. Aglaonema costatum var. maculatumEngl. = Aglaonema costatum N.E.Br, Ref.: Pflanzenr. 64 (IV.23Dc) (1915) 17 Type: Curtis 2813 (K, SING) Checklist of Malesian, Australian, and tropical western Pacific Araceae 5 Aglaonema crispum (Pitcher & Manda) Nicolson Syn.: Aglaonema roebeliniiPitcher & Manda, Schismatoglottis crispa Pitcher & Manda,Schismatoglottis roebelinii(Pitcher & Manda) Pitcher & Manda Ref.: Baileya 15 (1967) 126 Type: photograph labelled Schismatoglottis roebelinii, p. 141 in Pitcher & Manda, General Illustrated Catalogue of Plants (1895) (Neotype) Distr.: PHILIP (N) Aglaonema? cuscuaria (Aubl.) Miq. = Scindapsus cuscuaria (Aubl.) Presl Ref.: FI. Ned. Ind. 3 (1856) 217 Aglaonema densinervium Engl. Ref.: Bot. Jahrb. Syst. 37 (1906) 134 Type: Copeland 418 (B, US) Distr.: CELEBES (N), PHILIP (N) Aglaonema elegans Engl. = Aglaonema commutatum var. elegans (Engl.) Nicolson Ref.: Pflanzenr. 64 (IV.23Dc) (1915) 28 Aglaonema elongatum Alderw. = Aglaonema simplex Blume Ref.: Bull. Jard. Bot. Buitenzorg III, 4 (1922)
Recommended publications
  • 197-1572431971.Pdf
    Innovare Journal of Critical Reviews Academic Sciences ISSN- 2394-5125 Vol 2, Issue 2, 2015 Review Article EPIPREMNUM AUREUM (JADE POTHOS): A MULTIPURPOSE PLANT WITH ITS MEDICINAL AND PHARMACOLOGICAL PROPERTIES ANJU MESHRAM, NIDHI SRIVASTAVA* Department of Bioscience and Biotechnology, Banasthali University, Rajasthan, India Email: [email protected] Received: 13 Dec 2014 Revised and Accepted: 10 Jan 2015 ABSTRACT Plants belonging to the Arum family (Araceae) are commonly known as aroids as they contain crystals of calcium oxalate and toxic proteins which can cause intense irritation of the skin and mucous membranes, and poisoning if the raw plant tissue is eaten. Aroids range from tiny floating aquatic plants to forest climbers. Many are cultivated for their ornamental flowers or foliage and others for their food value. Present article critically reviews the growth conditions of Epipremnum aureum (Linden and Andre) Bunting with special emphasis on their ethnomedicinal uses and pharmacological activities, beneficial to both human and the environment. In this article, we review the origin, distribution, brief morphological characters, medicinal and pharmacological properties of Epipremnum aureum, commonly known as ornamental plant having indoor air pollution removing capacity. There are very few reports to the medicinal properties of E. aureum. In our investigation, it has been found that each part of this plant possesses antibacterial, anti-termite and antioxidant properties. However, apart from these it can also turn out to be anti-malarial, anti- cancerous, anti-tuberculosis, anti-arthritis and wound healing etc which are a severe international problem. In the present study, details about the pharmacological actions of medicinal plant E. aureum (Linden and Andre) Bunting and Epipremnum pinnatum (L.) Engl.
    [Show full text]
  • Araceae) in Bogor Botanic Gardens, Indonesia: Collection, Conservation and Utilization
    BIODIVERSITAS ISSN: 1412-033X Volume 19, Number 1, January 2018 E-ISSN: 2085-4722 Pages: 140-152 DOI: 10.13057/biodiv/d190121 The diversity of aroids (Araceae) in Bogor Botanic Gardens, Indonesia: Collection, conservation and utilization YUZAMMI Center for Plant Conservation Botanic Gardens (Bogor Botanic Gardens), Indonesian Institute of Sciences. Jl. Ir. H. Juanda No. 13, Bogor 16122, West Java, Indonesia. Tel.: +62-251-8352518, Fax. +62-251-8322187, ♥email: [email protected] Manuscript received: 4 October 2017. Revision accepted: 18 December 2017. Abstract. Yuzammi. 2018. The diversity of aroids (Araceae) in Bogor Botanic Gardens, Indonesia: Collection, conservation and utilization. Biodiversitas 19: 140-152. Bogor Botanic Gardens is an ex-situ conservation centre, covering an area of 87 ha, with 12,376 plant specimens, collected from Indonesia and other tropical countries throughout the world. One of the richest collections in the Gardens comprises members of the aroid family (Araceae). The aroids are planted in several garden beds as well as in the nursery. They have been collected from the time of the Dutch era until now. These collections were obtained from botanical explorations throughout the forests of Indonesia and through seed exchange with botanic gardens around the world. Several of the Bogor aroid collections represent ‘living types’, such as Scindapsus splendidus Alderw., Scindapsus mamilliferus Alderw. and Epipremnum falcifolium Engl. These have survived in the garden from the time of their collection up until the present day. There are many aroid collections in the Gardens that have potentialities not widely recognised. The aim of this study is to reveal the diversity of aroids species in the Bogor Botanic Gardens, their scientific value, their conservation status, and their potential as ornamental plants, medicinal plants and food.
    [Show full text]
  • Outline of Angiosperm Phylogeny
    Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese
    [Show full text]
  • 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.
    [Show full text]
  • A Taxonomic Revision of Araceae Tribe Potheae (Pothos, Pothoidium and Pedicellarum) for Malesia, Australia and the Tropical Western Pacific
    449 A taxonomic revision of Araceae tribe Potheae (Pothos, Pothoidium and Pedicellarum) for Malesia, Australia and the tropical Western Pacific P.C. Boyce and A. Hay Abstract Boyce, P.C. 1 and Hay, A. 2 (1Herbarium, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, U.K. and Department of Agricultural Botany, School of Plant Sciences, The University of Reading, Whiteknights, P.O. Box 221, Reading, RS6 6AS, U.K.; 2Royal Botanic Gardens, Mrs Macquarie’s Road, Sydney, NSW 2000, Australia) 2001. A taxonomic revision of Araceae tribe Potheae (Pothos, Pothoidium and Pedicellarum) for Malesia, Australia and the tropical Western Pacific. Telopea 9(3): 449–571. A regional revision of the three genera comprising tribe Potheae (Araceae: Pothoideae) is presented, largely as a precursor to the account for Flora Malesiana; 46 species are recognized (Pothos 44, Pothoidium 1, Pedicellarum 1) of which three Pothos (P. laurifolius, P. oliganthus and P. volans) are newly described, one (P. longus) is treated as insufficiently known and two (P. sanderianus, P. nitens) are treated as doubtful. Pothos latifolius L. is excluded from Araceae [= Piper sp.]. The following new synonymies are proposed: Pothos longipedunculatus Ridl. non Engl. = P. brevivaginatus; P. acuminatissimus = P. dolichophyllus; P. borneensis = P. insignis; P. scandens var. javanicus, P. macrophyllus and P. vrieseanus = P. junghuhnii; P. rumphii = P. tener; P. lorispathus = P. leptostachyus; P. kinabaluensis = P. longivaginatus; P. merrillii and P. ovatifolius var. simalurensis = P. ovatifolius; P. sumatranus, P. korthalsianus, P. inaequalis and P. jacobsonii = P. oxyphyllus. Relationships within Pothos and the taxonomic robustness of the satellite genera are discussed. Keys to the genera and species of Potheae and the subgenera and supergroups of Pothos for the region are provided.
    [Show full text]
  • Of Connecting Plants and People
    THE NEWSLEttER OF THE SINGAPORE BOTANIC GARDENS VOLUME 34, JANUARY 2010 ISSN 0219-1688 of connecting plants and people p13 Collecting & conserving Thai Convolvulaceae p2 Sowing the seeds of conservation in an oil palm plantation p8 Spindle gingers – jewels of Singapores forests p24 VOLUME 34, JANUARY 2010 Message from the director Chin See Chung ARTICLES 2 Collecting & conserving Thai Convolvulaceae George Staples 6 Spotlight on research: a PhD project on Convolvulaceae George Staples 8 Sowing the seeds of conservation in an oil palm plantation Paul Leong, Serena Lee 12 Propagation of a very rare orchid, Khoo-Woon Mui Hwang, Lim-Ho Chee Len Robiquetia spathulata Whang Lay Keng, Ali bin Ibrahim 150 years of connecting plants and people: Terri Oh 2 13 The making of stars Two minds, one theory - Wallace & Darwin, the two faces of evolution theory I do! I do! I do! One evening, two stellar performances In Search of Gingers Botanical diplomacy The art of botanical painting Fugitives fleurs: a unique perspective on floral fragments Falling in love Born in the Gardens A garden dialogue - Reminiscences of the Gardens 8 Children celebrate! Botanical party Of saints, ships and suspense Birthday wishes for the Gardens REGULAR FEATURES Around the Gardens 21 Convolvulaceae taxonomic workshop George Staples What’s Blooming 18 22 Upside down or right side up? The baobab tree Nura Abdul Karim Ginger and its Allies 24 Spindle gingers – jewels of Singapores forests Jana Leong-Škornicková From Education Outreach 26 “The Green Sheep” – a first for babies and toddlers at JBCG Janice Yau 27 International volunteers at the Jacob Ballas Children’s Garden Winnie Wong, Janice Yau From Taxonomy Corner 28 The puzzling bathroom bubbles plant..
    [Show full text]
  • Plant Life of Western Australia
    INTRODUCTION The characteristic features of the vegetation of Australia I. General Physiography At present the animals and plants of Australia are isolated from the rest of the world, except by way of the Torres Straits to New Guinea and southeast Asia. Even here adverse climatic conditions restrict or make it impossible for migration. Over a long period this isolation has meant that even what was common to the floras of the southern Asiatic Archipelago and Australia has become restricted to small areas. This resulted in an ever increasing divergence. As a consequence, Australia is a true island continent, with its own peculiar flora and fauna. As in southern Africa, Australia is largely an extensive plateau, although at a lower elevation. As in Africa too, the plateau increases gradually in height towards the east, culminating in a high ridge from which the land then drops steeply to a narrow coastal plain crossed by short rivers. On the west coast the plateau is only 00-00 m in height but there is usually an abrupt descent to the narrow coastal region. The plateau drops towards the center, and the major rivers flow into this depression. Fed from the high eastern margin of the plateau, these rivers run through low rainfall areas to the sea. While the tropical northern region is characterized by a wet summer and dry win- ter, the actual amount of rain is determined by additional factors. On the mountainous east coast the rainfall is high, while it diminishes with surprising rapidity towards the interior. Thus in New South Wales, the yearly rainfall at the edge of the plateau and the adjacent coast often reaches over 100 cm.
    [Show full text]
  • The Evolution of Pollinator–Plant Interaction Types in the Araceae
    BRIEF COMMUNICATION doi:10.1111/evo.12318 THE EVOLUTION OF POLLINATOR–PLANT INTERACTION TYPES IN THE ARACEAE Marion Chartier,1,2 Marc Gibernau,3 and Susanne S. Renner4 1Department of Structural and Functional Botany, University of Vienna, 1030 Vienna, Austria 2E-mail: [email protected] 3Centre National de Recherche Scientifique, Ecologie des Foretsˆ de Guyane, 97379 Kourou, France 4Department of Biology, University of Munich, 80638 Munich, Germany Received August 6, 2013 Accepted November 17, 2013 Most plant–pollinator interactions are mutualistic, involving rewards provided by flowers or inflorescences to pollinators. An- tagonistic plant–pollinator interactions, in which flowers offer no rewards, are rare and concentrated in a few families including Araceae. In the latter, they involve trapping of pollinators, which are released loaded with pollen but unrewarded. To understand the evolution of such systems, we compiled data on the pollinators and types of interactions, and coded 21 characters, including interaction type, pollinator order, and 19 floral traits. A phylogenetic framework comes from a matrix of plastid and new nuclear DNA sequences for 135 species from 119 genera (5342 nucleotides). The ancestral pollination interaction in Araceae was recon- structed as probably rewarding albeit with low confidence because information is available for only 56 of the 120–130 genera. Bayesian stochastic trait mapping showed that spadix zonation, presence of an appendix, and flower sexuality were correlated with pollination interaction type. In the Araceae, having unisexual flowers appears to have provided the morphological precon- dition for the evolution of traps. Compared with the frequency of shifts between deceptive and rewarding pollination systems in orchids, our results indicate less lability in the Araceae, probably because of morphologically and sexually more specialized inflorescences.
    [Show full text]
  • Giant Swamp Taro, a Little-Known Asian-Pacific Food Crop Donald L
    36 TROPICAL ROOT CROPS SYMPOSIUM Martin, F. W., Jones, A., and Ruberte, R. M. A improvement of yams, Dioscorea rotundata. wild Ipomoea species closely related to the Nature, 254, 1975, 134-135. sweet potato. Ec. Bot. 28, 1974,287-292. Sastrapradja, S. Inventory, evaluation and mainte­ Mauny, R. Notes historiques autour des princi­ nance of the genetic stocks at Bogor. Trop. pales plantes cultiVl!es d'Afrique occidentale. Root and Tuber Crops Tomorrow, 2, 1970, Bull. Inst. Franc. Afrique Noir 15, 1953, 684- 87-89. 730. Sauer, C. O. Agricultural origins and dispersals. Mukerjee, I., and Khoshoo, T. N. V. Genetic The American Geogr. Society, New York, 1952. evolutionary studies in starch yielding Canna Sharma, A. K., and de Deepesh, N. Polyploidy in edulis. Gen. Iber. 23, 1971,35-42. Dioscorea. Genetica, 28, 1956, 112-120. Nishiyama. I. Evolution and domestication of the Simmonds, N. W. Potatoes, Solanum tuberosum sweet potato. Bot. Mag. Tokyo, 84, 1971, 377- (Solanaceae). In Simmonds, N. W., ed., Evolu­ 387. tion of crop plants. Longmans, London, 279- 283, 1976. Nishiyama, I., Miyazaki, T., and Sakamoto, S. Stutervant, W. C. History and ethnography of Evolutionary autoploidy in the sweetpotato some West Indian starches. In Ucko, J. J., and (Ipomea batatas (L). Lam.) and its preogenitors. Dimsley, G. W., eds., The domestication of Euphytica 24, 1975, 197-208. plants and animals. Duckworth, London, 177- Plucknett, D. L. Edible aroids, A locasia, Colo­ 199, 1969. casia, Cyrtosperma, Xanthosoma (Araceae). In Subramanyan, K. N., Kishore, H., and Misra, P. Simmonds, N. W., ed., Evolution of crop plants. Hybridization of haploids of potato in the plains London, 10-12, 1976.
    [Show full text]
  • Full Text (PDF)
    12 Journal of Pharmaceutical, Chemical and Biological Sciences February 2014 ; 1(1):12-17 Available online at http://www.jpcbs.info Research Article Evaluation of Antidiabetic Activity from the Stem of Lasia spinosa in Dexamethasone Induced Diabetic Albino Rats. Sumit Das *, Mousumi Baruah , Dibyendu Shill Department of Pharmaceutical Chemistry, Girijananda Chowdhury Institute of Pharmaceutical Science, Guwahati, Assam- 781017 (India). ABSTRACT Diabetes mellitus is a chronic metabolic disease. It causes number of complications, like retinopathy, neuropathy and peripheral vascular insufficiencies. The worldwide prevalence of diabetes is expected to be more than 240 million by the year 2010. In India more than 30 million people are with diabetes mellitus. There are lots of synthetic agents available to treat Diabetes, but they have some undesirable side effects. Plant-based medicinal products have been known since ancient times and various medicinal plants and their products have been used to manage diabetes mellitus in the traditional medicinal systems of many countries in the world. Moreover, during the past few years many phyto-constituents which are responsible for antidiabetic activity have been isolated from the plant species. In the present study, an attempt was made to investigate the anti-diabetic activity of Lasia spinosa stem extracts (Hydroalcoholic extract) in different dosages (200 and 400 mg/kg b.w.) in dexamethasone induced diabetic albino rats and it shows potent antidiabetic activity against standard. Key words: Diabetes mellitus (DM), Dexamethasone, Hydroalcoholic extract Non-insulin dependent Diabetes mellitus (NIDDM), Hypoglycemia. Received: 24 January 2014 Revised and Accepted: 06 February 2014 * Corresponding author: Email: [email protected] Journal of Pharmaceutical, Chemical and Biological Sciences, February 2014; 1(1):12-17 Das et al 13 INTRODUCTION The World Health Organization Expert Committee Assam is rich in flora and diverse in its vegetation on diabetes has recommended that traditional types.
    [Show full text]
  • Studies on Schismatoglottideae (Araceae) of Borneo LIX – a Preliminary Conspectus of Schismatoglottis Calyptrata Complex Clade Species for Sarawak
    Wong, Hoe and Boyce, 2016 Studies on Schismatoglottideae (Araceae) of Borneo LIX ... Studies on Schismatoglottideae (Araceae) of Borneo LIX – A preliminary conspectus of Schismatoglottis Calyptrata Complex Clade species for Sarawak Wong Sin Yeng* Department of Plant Science & Environmental Ecology Faculty of Resource Science & Technology Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia [email protected] Associate Researcher Harvard University Herbaria 22 Divinity Avenue, Cambridge, MA 02138, USA *corresponding author Hoe Yin Chen Department of Plant Science & Environmental Ecology Faculty of Resource Science & Technology Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia Peter C. Boyce Ludwig–Maximilians–Universität München Department Biologie I Systematische Botanik und Mykologie Menzinger Straße 67, 80638 München, Germany [email protected] ABSTRACT Boyce is newly described, and S. muluensis A preliminary conspectus of species of M. Hotta is resurrected from within S. the Schismatoglottis Calyptrata Complex Clade calyptrata (Roxb.) Zoll. & Moritzi. Current for Sarawak is presented. Six species are evidence does not support the presence of accepted, of which Schismatoglottis Schismatoglottis calyptrata sens. strict. in Sarawak, baangongensis S.Y. Wong, Y.C. Hoe & P.C. while occurrence on Borneo as a whole is Aroideana VOL 39 NO 2, 2016 71 Wong, Hoe and Boyce, 2016 Studies on Schismatoglottideae (Araceae) of Borneo LIX ... questionable. A modified description of S. discrete segregate species was calyptrata, excluding characteristics of acknowledged, as below: Bornean taxa hitherto included in synonymy is provided. An identification key to the accepted species for Sarawak is provided, Sumatera and most are illustrated from living plants. Schismatoglottis ecaudata A. Hay Borneo – widespread KEY WORDS Geological obligation, Schismatoglottis Schismatoglottis ahmadii A.
    [Show full text]
  • Phylogenetic Study of the Schismatoglottis Nervosa Complex (Araceae: Schismatoglottideae)
    Gardens’ Bulletin Singapore 64(1): 211–219. 2012 211 Phylogenetic study of the Schismatoglottis Nervosa Complex (Araceae: Schismatoglottideae) A.P.J. Ting1,2, S.Y. Wong1, J. Jamliah1 and P.C. Boyce3 1Department of Plant Science & Environmental Ecology, Faculty of Resource Science & Technology, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia [email protected] 3Pusat Pengajian Sains Kajihayat (School of Biological Sciences), Universiti Sains Malaysia, 11800 USM, Pulau Pinang, Malaysia ABSTRACT. The Schismatoglottis Nervosa Complex (Araceae: Schismatoglottideae) currently comprises 10 species: Schismatoglottis adoceta S.Y.Wong, S. elegans A.Hay, S. liniae S.Y.Wong, S. tessellata S.Y.Wong, S. ulusarikeiensis S.Y.Wong, S. matangensis S.Y.Wong, S. simonii S.Y.Wong, S. turbata S.Y.Wong, and S. nervosa Ridl., occurring in Borneo, with each endemic to a specific locality and most to a particular geology; and one species (S. brevicuspis Hook.f.) widespread in Peninsular Malaysia and Sumatera, where it is restricted to granites. Based on analysis of the matK region, a preliminary biogeographical hypothesis for the origins and subsequent taxagenesis of the Nervosa Complex is presented. This study also provides insight into possible evolution of localised mesophytic endemics in everwet, humid, and perhumid megathermal Sundaic forests. Two clades are resolved: one north of, and another south of, the Lupar Divide. Keywords. Araceae, biogeography, Borneo, matK, Schismatoglottis Nervosa Complex, vicariance Introduction Geology and tectonics of Borneo Borneo is the third largest island in the world and the second largest tropical island after New Guinea. Borneo is situated in a tectonically intricate region between three marginal basins: the South China, Sulu and Celebes Seas (Hall et al.
    [Show full text]