Piquigua, Heteropsis Ecuadorensis Sodiro
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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. -
Understanding the Origin and Rapid Diversification of the Genus Anthurium Schott (Araceae), Integrating Molecular Phylogenetics, Morphology and Fossils
University of Missouri, St. Louis IRL @ UMSL Dissertations UMSL Graduate Works 8-3-2011 Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils Monica Maria Carlsen University of Missouri-St. Louis, [email protected] Follow this and additional works at: https://irl.umsl.edu/dissertation Part of the Biology Commons Recommended Citation Carlsen, Monica Maria, "Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils" (2011). Dissertations. 414. https://irl.umsl.edu/dissertation/414 This Dissertation is brought to you for free and open access by the UMSL Graduate Works at IRL @ UMSL. It has been accepted for inclusion in Dissertations by an authorized administrator of IRL @ UMSL. For more information, please contact [email protected]. Mónica M. Carlsen M.S., Biology, University of Missouri - St. Louis, 2003 B.S., Biology, Universidad Central de Venezuela – Caracas, 1998 A Thesis Submitted to The Graduate School at the University of Missouri – St. Louis in partial fulfillment of the requirements for the degree Doctor of Philosophy in Biology with emphasis in Ecology, Evolution and Systematics June 2011 Advisory Committee Peter Stevens, Ph.D. (Advisor) Thomas B. Croat, Ph.D. (Co-advisor) Elizabeth Kellogg, Ph.D. Peter M. Richardson, Ph.D. Simon J. Mayo, Ph.D Copyright, Mónica M. Carlsen, 2011 Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils Mónica M. Carlsen M.S., Biology, University of Missouri - St. Louis, 2003 B.S., Biology, Universidad Central de Venezuela – Caracas, 1998 Advisory Committee Peter Stevens, Ph.D. -
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. -
Ornamental Garden Plants of the Guianas, Part 3
; Fig. 170. Solandra longiflora (Solanaceae). 7. Solanum Linnaeus Annual or perennial, armed or unarmed herbs, shrubs, vines or trees. Leaves alternate, simple or compound, sessile or petiolate. Inflorescence an axillary, extra-axillary or terminal raceme, cyme, corymb or panicle. Flowers regular, or sometimes irregular; calyx (4-) 5 (-10)- toothed; corolla rotate, 5 (-6)-lobed. Stamens 5, exserted; anthers united over the style, dehiscing by 2 apical pores. Fruit a 2-celled berry; seeds numerous, reniform. Key to Species 1. Trees or shrubs; stems armed with spines; leaves simple or lobed, not pinnately compound; inflorescence a raceme 1. S. macranthum 1. Vines; stems unarmed; leaves pinnately compound; inflorescence a panicle 2. S. seaforthianum 1. Solanum macranthum Dunal, Solanorum Generumque Affinium Synopsis 43 (1816). AARDAPPELBOOM (Surinam); POTATO TREE. Shrub or tree to 9 m; stems and leaves spiny, pubescent. Leaves simple, toothed or up to 10-lobed, to 40 cm. Inflorescence a 7- to 12-flowered raceme. Corolla 5- or 6-lobed, bluish-purple, to 6.3 cm wide. Range: Brazil. Grown as an ornamental in Surinam (Ostendorf, 1962). 2. Solanum seaforthianum Andrews, Botanists Repository 8(104): t.504 (1808). POTATO CREEPER. Vine to 6 m, with petiole-tendrils; stems and leaves unarmed, glabrous. Leaves pinnately compound with 3-9 leaflets, to 20 cm. Inflorescence a many- flowered panicle. Corolla 5-lobed, blue, purple or pinkish, to 5 cm wide. Range:South America. Grown as an ornamental in Surinam (Ostendorf, 1962). Sterculiaceae Monoecious, dioecious or polygamous trees and shrubs. Leaves alternate, simple to palmately compound, petiolate. Inflorescence an axillary panicle, raceme, cyme or thyrse. -
Anadendrum (Araceae: Monsteroideae: Anadendreae) in Thailand
THAI FOR. BULL. (BOT.) 37: 1–8. 2009. Anadendrum (Araceae: Monsteroideae: Anadendreae) in Thailand PETER C. BOYCE1 ABSTRACT. As part of the Araceae project for the Flora of Thailand a study of Anadendrum was undertaken with the result that all three species hitherto collected in Thailand are considered to represent new taxa. A key to the lianescent aroid genera in Thailand and a key to Thai Anadendrum are presented. All species are illustrated. KEY WORDS: Araceae, Anadendrum, taxonomy, key, Flora of Thailand. INTRODUCTION Anadendrum is taxonomically by far the least-known lianescent aroid genus in tropical Asia. The problems besetting researchers are several-fold. To begin with, historical types are for the most part woefully inadequate. They were mainly preserved post anthesis so that the spathes are unknown for most of the described species. In addition field notes for the types (indeed for almost all existing specimens) are poor to effectively nonexistent and field sampling is patchy in the extreme. Lastly, groups of species that are immediately recognizable as distinct in nature look indistinguishable from one another when preserved. In essence, working from herbarium specimens alone is wholly inadequate but nonetheless time constraints mean that a workable account for the flora must be produced without recourse to a much-needed full scale, field-based revision. Given the above, I have opted for the pragmatic but unorthodox approach of not attempting to match Thai collections to any previously described species (a futile exercise in any case given the poor condition of almost all historical types) but instead have chosen to describe all species as new. -
Pollination by Nitidulid Beetles in the Hemi-Epiphytic Aroid Monstera Lentii (Araceae: Monsteroideae)
Flora 231 (2017) 57–64 Contents lists available at ScienceDirect Flora j ournal homepage: www.elsevier.com/locate/flora Original Research Pollination by nitidulid beetles in the hemi-epiphytic aroid Monstera lentii (Araceae: Monsteroideae) a b,∗ Danyi Prieto , Alfredo Cascante-Marín a Escuela de Ciencias Biológicas, Universidad Nacional de Costa Rica, Heredia, Costa Rica b Escuela de Biología, Universidad de Costa Rica, 11501-2060 San Pedro de Montes de Oca, San José, Costa Rica a r a t b i c s t l e i n f o r a c t Article history: Among aroids (Araceae family) with bisexual flowers, the reproductive biology of the neotropical genus Received 7 November 2016 Monstera (Subfamily Monsteroideae) is misunderstood. Nothing is known about the reproductive phe- Received in revised form 19 April 2017 nology and the sparse evidence on its pollination system is equivocal, suggesting both bees and beetles Accepted 19 April 2017 as pollinators. In order to elucidate the pollination system and reproductive behavior of Monstera, we Edited by Stefan Dötterl documented the floral cycle, spathe movement, floral visitors, and heat production of the inflorescence, Available online 24 April 2017 and the flowering and fruiting phenology of M. lentii in a montane forest in Costa Rica. We found that M. lentii was mainly visited and likely pollinated by nitidulid beetles (Cychrocephalus corvinus, Nitidulidae) Keywords: Cantharophily from the Mystropini tribe, which were mainly known as palm pollinators so far. In this mutualism, the beetles use the floral chamber as shelter, mating place, and probably as brood site. Drosophilid flies also Drosophilid flies Floral chamber visited the inflorescences and might participate in a mixed-pollination system, while stingless bees are Beetle pollination considered as pollen robbers. -
The Genus Amydrium (Araceae: Monsteroideae: Monstereae) With
KEWBULLETIN 54: 379 - 393 (1999) The genus Amydrium (Araceae: Monsteroideae:Monstereae) with particular reference to Thailand and Indochina NGUYENVAN Dzu'l & PETER C. BOYCE2 Summary. The genus Amydrium (Araceae) is recorded for the first time from Vietnam, with two species, A. hainanense and A. sinense, hitherto known only from China (including Hainan). Neither species was treated in the last revision of Amydrium(Nicolson 1968) and their recognition requires alterations to his account. A key to the Asian genera of Monstereaeand Anadendreae,an expanded generic description, keys to fertile, sterile and juvenile plants and a review of the genus is presented. Both newly recorded Vietnamese species are illustrated. INTRODUCTION AmydriumSchott, a genus of terrestrial subscandent herbs and root-climbing lianes occurring from Sumatra to New Guinea and from southern China to Java, was last revised by Nicolson (1968). Nicolson merged EpipremnopsisEngl. into the then monospecific Amydrium,recognizing four species in all. Since Nicolson's account two more species have been recognized: A. sinense (Engl.) H. Li and A. hainanense (C. C. Ting & C. Y Wu ex H. Li et al.) H. Li. Amydriumsinense, based upon Engler's Scindapsus sinensis (Engler 1900), was overlooked by Nicolson. Amydrium hainanense, described initially in Epipremnopsis(Li et al. 1977), was later transferred to Amydrium (Li 1979). Additionally, two species recognized by Nicolson, A. zippelianumand A. magnificum, have since been shown to be conspecific (Hay 1990; Boyce 1995). Amydriumas here defined comprises five species. Amydrium is currently placed in Monsteroideae tribe Monstereae (sensu Mayo et al. 1997) but has a chequered history of infrafamilial placement. In publishing Amydrium(then monospecific: A. -
History and Current Status of Systematic Research with Araceae
HISTORY AND CURRENT STATUS OF SYSTEMATIC RESEARCH WITH ARACEAE Thomas B. Croat Missouri Botanical Garden P. O. Box 299 St. Louis, MO 63166 U.S.A. Note: This paper, originally published in Aroideana Vol. 21, pp. 26–145 in 1998, is periodically updated onto the IAS web page with current additions. Any mistakes, proposed changes, or new publications that deal with the systematics of Araceae should be brought to my attention. Mail to me at the address listed above, or e-mail me at [email protected]. Last revised November 2004 INTRODUCTION The history of systematic work with Araceae has been previously covered by Nicolson (1987b), and was the subject of a chapter in the Genera of Araceae by Mayo, Bogner & Boyce (1997) and in Curtis's Botanical Magazine new series (Mayo et al., 1995). In addition to covering many of the principal players in the field of aroid research, Nicolson's paper dealt with the evolution of family concepts and gave a comparison of the then current modern systems of classification. The papers by Mayo, Bogner and Boyce were more comprehensive in scope than that of Nicolson, but still did not cover in great detail many of the participants in Araceae research. In contrast, this paper will cover all systematic and floristic work that deals with Araceae, which is known to me. It will not, in general, deal with agronomic papers on Araceae such as the rich literature on taro and its cultivation, nor will it deal with smaller papers of a technical nature or those dealing with pollination biology. -
Molecular and Physiological Role of Epipremnum Aureum
[Downloaded free from http://www.greenpharmacy.info on Tuesday, September 16, 2014, IP: 223.30.225.254] || Click here to download free Android application for this journal Molecular and physiological role of Epipremnum aureum TICLE R Anju Meshram, Nidhi Srivastava Department of Bioscience and Biotechnology, Banasthali University, Banasthali, Rajasthan, India A Epipremnum aureum (Golden pothos) is a naturally variegated climbing vine that produces abundant yellow-marbled foliage. It is among the most popular tropical ornamental plant used as hanging basket crop. An insight has been provided about the different varieties of Golden pothos including Neon, Marble Queen, Jade Pothos and N Joy. This paper presents a critical review on botanical study and important characteristics of Golden pothos and special emphasis has been provided on variegated leaves and chloroplast EVIEW biogenesis explaining the important genes involved during the process and various proteins associated with it. Studies have been included comprising the special features of Epipremnum aureum in phytoremediation for the removal of Cobalt and Cesium and in R the purification of air against formaldehyde. The antimicrobial activity of roots and leaf extracts of Epipremnum aureum against many bacterial strains have been included. It also presents the antitermite activity of Golden pothos that can be harnessed for pest control. Key words: Antimicrobial, antitermite, calcium oxalate, Epipremnum aureum, formaldehyde INTRODUCTION Other Species of Epipremnum • Epipremnum amplissimum (Schott) Engl Epipremnum comprises 15 speciesof slender to gigantic • Epipremnum amplissimum (Schott) Engl root‑climbing Iianes.[1] All these herbaceous evergreens • Epipremnum carolinense Volkens are native to South East Asia and Solomon islands.[2] • Epipremnum ceramense (Engl. -
An Introduction to Aroid Genera
An Introduction to Aroid Genera by Tom Croat Gymnostachys Subfamilies of Araceae anceps 1 sp. • Proto-Araceae Australia I. Subfamily Gymnostachydoideae – Gymnostachys II. Subfamily Orontioideae – Orontium – Lysichiton – Symplocarpus Lysichiton camchatsense 2 sp. W. Orontium aquaticum N. Amer 3 sp. W. & E. Asia N. Amer. & 1 sp. E. E. Asia N. Amer. Symplocarpus foetidus Orontium aquaticum, 57207 Lysichiton camtschatsense Lysichiton camtschatsense Lysichiton camtschatsense Symplocarpus foetidus, 790539 Symplocarpus foetidus Symplocarpus foetidus, MBG 790539 Symplocarpus foetidus True Araceae III. Subfamily Pothoideae – Tribe Pothoeae • Pothos – Tribe Anthurieae Pothos • Anthurium scandens , Anthurium antioquense Pothos, Croat 77332 Pothos scandens Pothos scandens Pothos chinensis Anthurium corrugatum Anthurium sect. Pachyneurium Anthurium 49788 Subfamily Monsteroideae • Tribe Spathiphylleae – Spathiphyllum – Holochlamys • Tribe Anadendreae Spathiphyllum floribundum – Anadendron • Tribe Heteropsidae – Heteropsis Holochlamys beccari Anadendrum Heteropsis spruceana Anadendrum Spathiphyllum brevirostre Spathiphylllum wendlandii Spathiphyllum floribundum Spathiphyllum floribundum Spathiphyllum humboldtii Spathiphyllum coclearispathum Spathiphylllum patulinervia Subfamily Monsteroideae • Tribe Monstereae – Amydrium – Rhaphidophora – Epipremnum Amydrium Rhaphidophora magnificum – Scindapsus pinnata – Monstera – Alloschemone – Rhodospatha – Stenospermation Epipremnum pinnatum Scindapsus exotica _ Monstera Rhodospatha Stenospermation marantifolium -
The Genus Rhaphidophora Hassk. (Araceae-Monsteroideae-Monstereae) in Peninsular Malaysia and Singapore
Gardens' Bulletin Singapore 51 (1999) 183-256. The Genus Rhaphidophora Hassk. (Araceae-Monsteroideae-Monstereae) in Peninsular Malaysia and Singapore P.C. BOYCE Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, U.K. Abstract An alpha-taxonomic account of Rhaphidophora in Peninsular Malaysia and Singapore is presented as a precursor to the forthcoming Flora Malesiana Araceae treatment. Fifteen species, two newly described, R. corneri, and R. nicolsonii, are recognized. An extensive new synonymy is proposed: R. pteropoda (syn. Scindapsus pteropodus) is synonymized with R. angustata; R. celatocaulis (syn. Pothos celatocaulis), R. copelandii, R. korthalsii var. angustiloba, R. latifolia, R. maxima, R. palawanensis Furtado non Merr., R. ridleyi (syn. R. grandis Ridl. non Schott), R. tenuis, and R. trinervia with R. korthalsii; R. fluminea with R. beccarii; R. apiculata Alderw. non K. Krause with R. maingayi; R. celebica with R. minor; R. burkilliana with R. montana; R. batoensis, R. gracilipes, R. hallieri, R. kunstleri, R. megasperma, R. pilosula, and R, scortechinii with R. puberula; R. gratissima (syn. R. sylvestris var, obtusata), R. lingulata (syn. Monstera lingulata, Scindapsus lingulatus), R. motleyana, R. wrayi, and Scindapsus aruensis with R. sylvestris. Dichotomous keys to genera and species are provided. All species except R. falcata are illustrated. Contents Introduction ...................................................................................................184 History .............................. .......................................................................184 -
English Contents
ENGLISH CONTENTS (for Color Plates, see pages 27–50) Participants ............................................................................ 174 Apéndices/Appendices (1) Geological Formations ....................................................... 296 Institutional Profiles ............................................................... 178 (2) Water Samples ................................................................... 300 Acknowledgments ................................................................... 182 (3) Vascular Plants .................................................................. 304 Mission and Approach ............................................................ 186 (4) Fish Sampling Stations ....................................................... 330 (5) Fishes ................................................................................ 332 Report at a Glance .................................................................. 187 (6) Amphibians and Reptiles ................................................... 346 Why Ere-Campuya-Algodón?.................................................... 198 (7) Birds ................................................................................. 362 Conservation Targets .............................................................. 199 (8) Large and Medium-sized Mammals ................................... 374 Assets and Opportunities ........................................................ 202 (9) Commonly Used Plants .....................................................