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Medicinal Practices of Sacred Natural Sites: a Socio-Religious Approach for Successful Implementation of Primary
Medicinal practices of sacred natural sites: a socio-religious approach for successful implementation of primary healthcare services Rajasri Ray and Avik Ray Review Correspondence Abstract Rajasri Ray*, Avik Ray Centre for studies in Ethnobiology, Biodiversity and Background: Sacred groves are model systems that Sustainability (CEiBa), Malda - 732103, West have the potential to contribute to rural healthcare Bengal, India owing to their medicinal floral diversity and strong social acceptance. *Corresponding Author: Rajasri Ray; [email protected] Methods: We examined this idea employing ethnomedicinal plants and their application Ethnobotany Research & Applications documented from sacred groves across India. A total 20:34 (2020) of 65 published documents were shortlisted for the Key words: AYUSH; Ethnomedicine; Medicinal plant; preparation of database and statistical analysis. Sacred grove; Spatial fidelity; Tropical diseases Standard ethnobotanical indices and mapping were used to capture the current trend. Background Results: A total of 1247 species from 152 families Human-nature interaction has been long entwined in has been documented for use against eighteen the history of humanity. Apart from deriving natural categories of diseases common in tropical and sub- resources, humans have a deep rooted tradition of tropical landscapes. Though the reported species venerating nature which is extensively observed are clustered around a few widely distributed across continents (Verschuuren 2010). The tradition families, 71% of them are uniquely represented from has attracted attention of researchers and policy- any single biogeographic region. The use of multiple makers for its impact on local ecological and socio- species in treating an ailment, high use value of the economic dynamics. Ethnomedicine that emanated popular plants, and cross-community similarity in from this tradition, deals health issues with nature- disease treatment reflects rich community wisdom to derived resources. -
GYNOECEUM MORPHOLOGY, EMBRYOLOGY and SYSTEMATIC POSITION of the GENUS ERYTHROPALUM by FOLKE FAGERLIND. Introduction the Genus Er
Fagerlind F. 1946. Gynöceummorphologische, embryologie und systematische stellung der gattung Erythropalum. Svensk Botanisk Tidskrift 40: 9-14. GYNOECEUM MORPHOLOGY, EMBRYOLOGY AND SYSTEMATIC POSITION OF THE GENUS ERYTHROPALUM BY FOLKE FAGERLIND. Introduction The genus Erythropalum has been described by BLUME (1826). He included it in the family Cucurbitaceae. Later, systematists have placed the genus in different plant families. Part of them considered it to be a member of its own family, Erythropalaceae. The views on the position of the genus or family are shown in the following summary: 1. The family is completely alone (PLANCHON 1854). 2. The genus belongs to Cucurbitaceae (BLUME 1826, DE CANDOLLE 1828, HASSKAHL 1848). 3. The family joins Cucurbitaceae, Passifloreae and Papayaceae (MIQUEL 1855). 4. The genus belongs to Olacaceae (ARNOTT 1838, BENTHAM and HOOKER 1862, VALETON 1886, ENGLER 1889, KOORDERS 1912, RIDLEY 1922, MERRIL 1923). 5. The family joins Olacaceae (VAN TIEGHEM 1896, 1897, GAGNEPAIN 1910, LECOMTE 1907-1912). 6. The genus is related to Vitis (BAILLON 1892, he made Vitis the tribe Viteae and Erythropalum the tribe Erythropaleae and summarized together these two tribes and Olacaceae, Santalaceae, Loranthaceae and others in the family Loranthaceae). 7. The genus is brought together with various Olacaceae, Opiliaceae and Icacinaceae to form a family that is placed in the neighborhood of families that are today classified in Therebinthales and Celastrales (MASTERS 1872-75). 8. The family joins Icacinaceae (GAGNEPAIN 1910, LECOMTE 1907-1912, SLEUMER 1935, 1942). In Buitenzorg's botanical garden a few individuals of Erythropalum scandens BLUME grow. During my stay in Java (1938), I collected material from them in order, if possible, to gain clarity about the correct position of the genus in the system by examining the gynoecium, the ovule, and the megagametophytes. -
Threatened Endemic Plants of Palau
THREA TENED ENDEMIC PLANTS OF PALAU BIODI VERSITY CONSERVATION LESSONS LEARNED TECHNICAL SERIES 19 BIODIVERSITY CONSERVATION LESSONS LEARNED TECHNICAL SERIES 19 Threatened Endemic Plants of Palau Biodiversity Conservation Lessons Learned Technical Series is published by: Critical Ecosystem Partnership Fund (CEPF) and Conservation International Pacific Islands Program (CI-Pacific) PO Box 2035, Apia, Samoa T: + 685 21593 E: [email protected] W: www.conservation.org The Critical Ecosystem Partnership Fund is a joint initiative of l’Agence Française de Développement, Conservation International, the Global Environment Facility, the Government of Japan, the MacArthur Foundation and the World Bank. A fundamental goal is to ensure civil society is engaged in biodiversity conservation. Conservation International Pacific Islands Program. 2013. Biodiversity Conservation Lessons Learned Technical Series 19: Threatened Endemic Plants of Palau. Conservation International, Apia, Samoa Authors: Craig Costion, James Cook University, Australia Design/Production: Joanne Aitken, The Little Design Company, www.thelittledesigncompany.com Photo credits: Craig Costion (unless cited otherwise) Cover photograph: Parkia flowers. © Craig Costion Series Editors: Leilani Duffy, Conservation International Pacific Islands Program Conservation International is a private, non-profit organization exempt from federal income tax under section 501c(3) of the Internal Revenue Code. OUR MISSION Building upon a strong foundation of science, partnership and field demonstration, -
9 Costion Plant Endemism 133-166 PROOFS
Micronesica 41(1): 131–164, 2009 Plant Endemism, Rarity, and Threat in Palau, Micronesia: A Geographical Checklist and Preliminary Red List Assessment 1 CRAIG M. COSTION Department of Ecology and Evolutionary Biology, School of Earth and Environmental Sciences, University of Adelaide, Adelaide SA 5001 [email protected] ANN HILLMANN KITALONG The Environment, Inc., P.O. Box 1696, Koror, Palau 96940 TARITA HOLM Palau Conservation Society/PALARIS, P.O. Box 1811, Koror, Palau, 96940 Abstract—An official checklist of the endemic plant species of Palau has been long awaited, and is presented here for the first time. For each species a substrate limitation, growth form, and relative abundance is listed. In addition an IUCN red list assessment was conducted using all available data. For over half of the endemic species there is insufficient data to provide a red listing status however an expected minimum number of threatened plants out of the total is inferred. Approximately 15% of Palau’s endemic plants are believed to be only known from the type collection and many more only known from a few collections. These taxa however may now be prioritized and targeted for future inventory and research. The taxonomic robustness of several of these taxa is questionable and it is expected that more endemic species will be lost to synonymy in the future. Previous estimations have significantly over-estimated the rate of plant endemism in Palau (e.g., 194). Here, 130 plants are recognized for Palau, making its level of plant endem- ism comparable to some of its neighboring Micronesian islands to the east, notably Guam and Pohnpei. -
The Embryology of <Emphasis Type="Italic">Ximenia Americana
Prec. Indian Acad. Sci,, Vol. 87 B, No. 2, February 1978, pp. 23-27, 9 Printed in India. The embryology of Ximenia americana L. K SANKARA RAO and G SHIVARAMIAH Department of Botany, St. Joseph's College, Bangalore 560 001 MS received 18 July 1977; revised 2 November 1977 Abstract. Olacaceae, Ximenia americana L.--Embryology. Anther tapetum glandu- lar. Endothecium fibrous. Cytokinesis in microsporocytes simultaneous. Pollen dimorphic, two-celled. Ovules ategmic, crassinucellar. Embryo sac Polygonum type, produces a haustorial caecum. A comparison with earlier investigations pre- sented. Keywords. Ximenia americana; embryology. 1. Introduction A perusal of the literature reveals that there are no adequate embryological data on the family Olacaceae except for the significant contributions by Fagerlind (1947), Shamanna (1954, 1961) and Agarwal (1961, 1963a, b). The present paper deals with aspects on the embryology of Ximenia americana L. 2. Materials and methods Flower buds at different stages of development were collected from Bannerghatta National Park, Bangalore, and fixed in FAA. Customary methods of dehydration and embedding were followed. Sections were cut at 8-12/zm and stained with Heidenhain's haematoxylin and counterstained with erythrosin. 3. Observations The creamy white flowers are 4--5-merous, actinomorphic, bisexual and hypogynous. Petals are hairy and reflexed. Stamens are twice as many as petals. Anthers are dithecous. Ovary is sessile and incompletely 3-4-celled each with one pendulous ovule (figures I-7). Anthers are tetrasporangiate. A transection of a young anther shows the epider- mis, endothecium, a middle layer and tapetum around the sporogenous tissue (figure 8). The tapetum is of the glandular type and its cells remain uninucleate throughout. -
University of Copenhagen, Rolighedsvej 25, 1958 Frederiksberg, Denmark
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Copenhagen University Research Information System 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. Download date: 08. Apr. 2020 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 -
Evolution of Angiosperm Pollen. 5. Early Diverging Superasteridae
Evolution of Angiosperm Pollen. 5. Early Diverging Superasteridae (Berberidopsidales, Caryophyllales, Cornales, Ericales, and Santalales) Plus Dilleniales Author(s): Ying Yu, Alexandra H. Wortley, Lu Lu, De-Zhu Li, Hong Wang and Stephen Blackmore Source: Annals of the Missouri Botanical Garden, 103(1):106-161. Published By: Missouri Botanical Garden https://doi.org/10.3417/2017017 URL: http://www.bioone.org/doi/full/10.3417/2017017 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/ page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non- commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. EVOLUTION OF ANGIOSPERM Ying Yu,2 Alexandra H. Wortley,3 Lu Lu,2,4 POLLEN. 5. EARLY DIVERGING De-Zhu Li,2,4* Hong Wang,2,4* and SUPERASTERIDAE Stephen Blackmore3 (BERBERIDOPSIDALES, CARYOPHYLLALES, CORNALES, ERICALES, AND SANTALALES) PLUS DILLENIALES1 ABSTRACT This study, the fifth in a series investigating palynological characters in angiosperms, aims to explore the distribution of states for 19 pollen characters on five early diverging orders of Superasteridae (Berberidopsidales, Caryophyllales, Cornales, Ericales, and Santalales) plus Dilleniales. -
1965) 278-307 Haustorium, (Loranthaceae
Acta Botanica Neerlandica 14 (1965) 278-307 On the Nature and Action of the Santalalean Haustorium, as exemplified by Phthirusa and Antidaphne (Loranthaceae) Job Kuijt {Department of Botany, University of British Columbia, Vancouver, Canada) (received June 30th, 1965) Abstract The original intent ofthe present study was an inquiry into the architecture of the secondary haustoria of the mistletoes Antidaphne viscoidea and Phthirusa pyrifolia, each representing one of the two subfamilies ofLoranthaceae. In the course of this study it fundamental has become clear that there are similarities uniting the haustoria of the entire order, Santalales. The needfor integration of all knowledge of Santalalean haustoria became the work and more pressing as proceeded has culminatedin this article form. in its present This work, then, represents an integrated review of the structure mechanism of Santalalean and haustoria, introduced by anaccount of the haustoria of Phthirusa and Antidaphne. Phthirusa and Antidaphne the The mistletoe haustorium of temperate zones is a direct out- growth of the radicular apex of the seedling. Even such complex those of absorptive systems as Arceuthobium, Phrygilanthus aphyllus, and some species of Phoradendron can be traced back to their origin from the apical meristem of the primary root. In a large numberof tropical and some subtropical Loranthaceae, however, secondary roots are formed from the base of the plant or from branches. Such roots are known as the the epicortical roots, and follow branches of host, producing secon- dary haustoria at irregular intervals. Secondary haustoria, partly their limited have received little through geographic occurrence, attention from anatomists. The present account of the young secon- dary haustoria of Phthirusa pyrifolia (HBK) Eichl. -
Hondurodendron, a New Monotypic Genus of Aptandraceae From
HONDURODENDRON, Carmen Ulloa Ulloa,2 Daniel L. Nickrent,3 A NEW MONOTYPIC GENUS Caroline Whitefoord,4 and Daniel L. Kelly5 OF APTANDRACEAE FROM HONDURAS1 ABSTRACT Hondurodendron C. Ulloa, Nickrent, Whitef. & D. Kelly, a new monotypic genus endemic to Honduras, is here described and illustrated. The new species, H. urceolatum C. Ulloa, Nickrent, Whitef. & D. Kelly, is a dioecious tree, distinguished by its minute flowers borne on densely tomentose inflorescences, unique anthers opening by three valves, and a characteristic fruit totally enveloped by the accrescent calyx, which projects beyond the fruit. A molecular analysis based on four genes (nuclear small subunit [SSU] ribosomal DNA [rDNA], chloroplast rbcL, matK, and accD) placed this genus in a clade with Aptandra Miers, Harmandia Pierre ex Baill., Chaunochiton Benth., and Ongokea Pierre in the family Aptandraceae Miers. RESUMEN Se describe e ilustra un nuevo ge´nero monotı´pico Hondurodendron C. Ulloa, Nickrent, Whitef. & D. Kelly ende´mico de Honduras. La nueva especie H. urceolatum C. Ulloa, Nickrent, Whitef. & D. Kelly es un a´rbol dioico, que se distingue por las flores diminutas en inflorescencias densamente tomentosas, las anteras u´nicas que se abren por tres valvas y un fruto caracterı´stico totalmente encerrado por el ca´liz acrescente que se proyecta sobre e´ste. Un ana´lisis molecular con cuatro genes (SSU ADN riboso´mico nuclear, rbcL del cloroplasto, matK y accD) ubica al ge´nero en un clado junto con Aptandra Miers, Harmandia Pierre ex Baill., Chaunochiton Benth. y Ongokea Pierre en la familia Aptandraceae Miers. Key words: Aptandraceae, Cusuco National Park, Honduras, Hondurodendron, IUCN Red List, Olacaceae. -
Ecological Aspects of the Cretaceous Flowering Plant Radiation1
Aww. Akv. EarfA f/o««f. Sci. 799& 26. J7V-/J/ ECOLOGICAL ASPECTS OF THE CRETACEOUS FLOWERING PLANT RADIATION1 Scott L. Wing and Lisa D. Boucher Department of Paleobiology, NHB121, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560; e-mail: [email protected], boucherl @ nmnh. si.edu KEY WORDS: angiosperms, Cretaceous, paleoecology, diversification, evolution ABSTRACT The first flowering plant fossils occur as rare, undiverse pollen grains in the Early Cretaceous (Valanginian-Hauterivian). Angiosperms diversified slowly during the Barremian-Aptian but rapidly during the Albian-Cenomanian. By the end of the Cretaceous, at least half of the living angiosperm orders were present, and angiosperms were greater than 70% of terrestrial plant species globally. The rapid diversification of the group, and its dominance in modern vegetation, has led to the idea that the Cretaceous radiation of angiosperms also represents their rise to vegetational dominance. Paleoecological data cast a different light on the Cretaceous radiation of an- giosperms. Analyses of sedimentary environments indicate that angiosperms not only originated in unstable habitats but remained centered there through most of the Cretaceous. Morphology of leaves, seeds, and wood is consistent with the status of most Cretaceous angiosperms as herbs to small trees with early successional strategy. The diversification of flowering plants in the Cretaceous represents the evolution of a highly speciose clade of weeds but not necessarily a major change in global vegetation. INTRODUCTION Flowering plants, or angiosperms, are presently the most dominant group of terrestrial autotrophs. They span an array of habits including very large trees, 1 The US Government has the right to retain a nonexclusive, royalty-free license in and to any copyright covering this paper. -
Perennial Edible Fruits of the Tropics: an and Taxonomists Throughout the World Who Have Left Inventory
United States Department of Agriculture Perennial Edible Fruits Agricultural Research Service of the Tropics Agriculture Handbook No. 642 An Inventory t Abstract Acknowledgments Martin, Franklin W., Carl W. Cannpbell, Ruth M. Puberté. We owe first thanks to the botanists, horticulturists 1987 Perennial Edible Fruits of the Tropics: An and taxonomists throughout the world who have left Inventory. U.S. Department of Agriculture, written records of the fruits they encountered. Agriculture Handbook No. 642, 252 p., illus. Second, we thank Richard A. Hamilton, who read and The edible fruits of the Tropics are nnany in number, criticized the major part of the manuscript. His help varied in form, and irregular in distribution. They can be was invaluable. categorized as major or minor. Only about 300 Tropical fruits can be considered great. These are outstanding We also thank the many individuals who read, criti- in one or more of the following: Size, beauty, flavor, and cized, or contributed to various parts of the book. In nutritional value. In contrast are the more than 3,000 alphabetical order, they are Susan Abraham (Indian fruits that can be considered minor, limited severely by fruits), Herbert Barrett (citrus fruits), Jose Calzada one or more defects, such as very small size, poor taste Benza (fruits of Peru), Clarkson (South African fruits), or appeal, limited adaptability, or limited distribution. William 0. Cooper (citrus fruits), Derek Cormack The major fruits are not all well known. Some excellent (arrangements for review in Africa), Milton de Albu- fruits which rival the commercialized greatest are still querque (Brazilian fruits), Enriquito D. -
Flowering Plants of Samoa
FLOWERING PLANTS OF SAMOA BY ERLING CHRISTOPHERSEN HONOLULU, HAWAII PUBLISHEDBY THE MUSEUM February 21, 1935 KRAUS REPRINT CO. New York 1971 CONTENTS PAGS Introduction ...................................................................................................................................... 3 Mono~otyledon~ae.......................................................................................................................... 6 Family 1. Pandanaceae ........................................................................................................ 6 Family 2. Hydrocharitaceae 6 Family 3. Gramineae ............................................................................................................ 6 Family 4. Cyperageae .......................................................................................................... 15 Family 5. Palmae .................................................................................................................. 25 Family 6- Araceae ................................................................................................................ 39 Family 7. Lemnaceae ............................................................................................................ 44 Family 8. Flagellariaceae 44 Family g. Bromeliaceae ...................................................................................................... 47 Family lo. Commelinaceae .................................................................................................. 48 . Family