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PHYTOCHEMICAL and PHARMACOLOGICAL PROFILING of Dysphania Botrys L
PHYTOCHEMICAL AND PHARMACOLOGICAL PROFILING OF Dysphania botrys L. BY MUHAMMAD NAEEM KHAN A dissertation submitted to The University of Agriculture Peshawar, in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY IN BIOTECHNOLOGY AND GENETIC ENGINEERING INSTITUTE OF BIOTECHNOLOGY & GENETIC ENGINEERING FACULTY OF CROP PRODUCTION SCIENCES THE UNIVERSITY OF AGRICULTURE PESHAWAR, PAKISTAN AUGUST, 2018 PHYTOCHEMICAL AND PHARMACOLOGICAL PROFILING OF Dysphania botrys L. BY MUHAMMAD NAEEM KHAN A dissertation submitted to The University of Agriculture Peshawar, in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY IN BIOTECHNOLOGY AND GENETIC ENGINEERING APPROVED BY: Chairman Supervisory Committee Dr. Asad Jan Associate Professor Co-Supervisor for Research Dr. Inamullah Khan Assistant Professor Pharmacy (UOP) Member Major Field Dr. Safdar Hussain Shah Member Minor Field Prof. Dr. Farhatullah Chairman and Convener Board of Studies Prof. Dr. Iqbal Munir Dean Faculty of Crop Production Sciences Prof. Dr. Zahir Shah Director Advanced Studies and Research Dr. Shahid Sattar INSTITUTE OF BIOTECHNOLOGY & GENETIC ENGINEERING FACULTY OF CROP PRODUCTION SCIENCES THE UNIVERSITY OF AGRICULTURE PESHAWAR, PAKISTAN AUGUST, 2018 TABLE OF CONTENTS S. No. Title Page No. List of Tables .......................................................................................... i List of Figures ....................................................................................... iii Abbreviations ........................................................................................ -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
A Review of Botany, Phytochemical, and Pharmacological Effects of Dysphania Ambrosioides
Indonesian Journal of Life Sciences Vol. 02 | Number 02 | September (2020) http://journal.i3l.ac.id/ojs/index.php/IJLS/ REVIEW ARTICLE A Review of Botany, Phytochemical, and Pharmacological Effects of Dysphania ambrosioides Lavisiony Gracius Hewis1, Giovanni Batista Christian Daeli1, Kenjiro Tanoto1, Carlos1, Agnes Anania Triavika Sahamastuti1* 1Pharmacy study program, Indonesia International Institute for Life-sciences, Jakarta, Indonesia *corresponding author. Email: [email protected] ABSTRACT Traditional medicine is widely used worldwide due to its benefits and healthier components that these natural herbs provide. Natural products are substances produced or retrieved from living organisms found in nature and often can exert biological or pharmacological activity, thus making them a potential alternative for synthetic drugs. Natural products, especially plant-derived products, have been known to possess many beneficial effects and are widely used for the treatment of various diseases and conditions. Dysphania ambrosioides is classified as an annual or short-lived perennial herb commonly found in Central and South America with a strong aroma and a hairy characteristic. Major components in this herb are ascaridole, p-cymene, α-terpinene, terpinolene, carvacrol, and trans-isoascaridole. Active compounds isolated from this herb are found to exert various pharmacological effects including schistosomicidal, nematicidal, antimalarial, antileishmanial, cytotoxic, antibacterial, antiviral, antifungal, antioxidant, anticancer, and antibiotic modulatory activity. This review summarizes the phytochemical compounds found in the Dysphania ambrosioides, together with their pharmacological and toxicological effects. Keywords: Dysphania ambrosioides; phytochemicals; pharmacological effect; secondary metabolites; toxicity INTRODUCTION pharmacologically-active compound, morphine, Natural products have been used by a wide was isolated from plants by Serturner spectrum of populations to alleviate and treat (Krishnamurti & Rao, 2016). -
(Amaranthaceae) in Italy. V. Atriplex Tornabenei
Phytotaxa 145 (1): 54–60 (2013) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2013 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.145.1.6 Studies on the genus Atriplex (Amaranthaceae) in Italy. V. Atriplex tornabenei DUILIO IAMONICO1 1 Laboratory of Phytogeography and Applied Geobotany, Department PDTA, Section Environment and Landscape, University of Rome Sapienza, 00196 Roma, Italy. Email: [email protected] Abstract The typification of the name Atriplex tornabenei (a nomen novum pro A. arenaria) is discussed. An illustration by Cupani is designated as the lectotype, while a specimen from FI is designated as the epitype. Chorological and morphological notes in comparison with the related species A. rosea and A. tatarica are also provided. A nomenclatural change (Atriplex tornabenei subsp. pedunculata stat. nov.) is proposed. Key words: Atriplex tornabenei var. pedunculata, epitype, infraspecific variability, lectotype, Mediterranean, nomenclatural change, nomen novum Introduction Atriplex Linnaeus (1753: 1054) is a genus of about 260 species distributed in arid and semiarid regions of Eurasia, America and Australia (Sukhorukov & Danin 2009). Several names (at species, subspecies, variety and form ranks) were described related to the high phenotipic variability of this critical genus (Al-Turki et al. 2000). As conseguence, misapplication of names and nomenclatural disorders exist and need clarification. In this paper, the identity of the A. tornabenei Tineo ex Gussone (1843: 589) is discussed as part of the treatment of the genus Atriplex for the new edition of the Italian Flora (editor, Prof. S. Pignatti) and within the initiative “Italian Loci Classici Census” (Domina et al. -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
CHENOPODIACEAE 藜科 Li Ke Zhu Gelin (朱格麟 Chu Ge-Ling)1; Sergei L
Flora of China 5: 351-414. 2003. CHENOPODIACEAE 藜科 li ke Zhu Gelin (朱格麟 Chu Ge-ling)1; Sergei L. Mosyakin2, Steven E. Clemants3 Herbs annual, subshrubs, or shrubs, rarely perennial herbs or small trees. Stems and branches sometimes jointed (articulate); indumentum of vesicular hairs (furfuraceous or farinose), ramified (dendroid), stellate, rarely of glandular hairs, or plants glabrous. Leaves alternate or opposite, exstipulate, petiolate or sessile; leaf blade flattened, terete, semiterete, or in some species reduced to scales. Flowers monochlamydeous, bisexual or unisexual (plants monoecious or dioecious, rarely polygamous); bracteate or ebracteate. Bractlets (if present) 1 or 2, lanceolate, navicular, or scale-like. Perianth membranous, herbaceous, or succulent, (1–)3–5- parted; segments imbricate, rarely in 2 series, often enlarged and hardened in fruit, or with winged, acicular, or tuberculate appendages abaxially, seldom unmodified (in tribe Atripliceae female flowers without or with poorly developed perianth borne between 2 specialized bracts or at base of a bract). Stamens shorter than or equaling perianth segments and arranged opposite them; filaments subulate or linear, united at base and usually forming a hypogynous disk, sometimes with interstaminal lobes; anthers dorsifixed, incumbent in bud, 2-locular, extrorse, or dehiscent by lateral, longitudinal slits, obtuse or appendaged at apex. Ovary superior, ovoid or globose, of 2–5 carpels, unilocular; ovule 1, campylotropous; style terminal, usually short, with 2(–5) filiform or subulate stigmas, rarely capitate, papillose, or hairy on one side or throughout. Fruit a utricle, rarely a pyxidium (dehiscent capsule); pericarp membranous, leathery, or fleshy, adnate or appressed to seed. Seed horizontal, vertical, or oblique, compressed globose, lenticular, reniform, or obliquely ovoid; testa crustaceous, leathery, membranous, or succulent; embryo annular, semi-annular, or spiral, with narrow cotyledons; endosperm much reduced or absent; perisperm abundant or absent. -
Notes on <I>Atriplex, Oxybasis</I> and <I>Dysphania</I
Plant Ecology and Evolution 149 (2): 249–256, 2016 http://dx.doi.org/10.5091/plecevo.2016.1181 SHORT COMMUNICATION Notes on Atriplex, Oxybasis and Dysphania (Chenopodiaceae) in West-Central Tropical Africa Alexander P. Sukhorukov1,*, Maria Kushunina2 & Filip Verloove3 1Department of Higher Plants, Biological Faculty, Lomonosov Moscow State University, 119234, Moscow, Russian Federation 2Department of Plant Physiology, Biological Faculty, Lomonosov Moscow State University, 119234, Moscow, Russian Federation 3Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium *Author for correspondence: [email protected] Background and aims – The indigenous representatives of Chenopodiaceae in tropical Africa are still insufficiently studied. Some genera, especially Atriplex L., Oxybasis Kar. & Kir. and Dysphania R.Br. (subfam. Chenopodioideae), are difficult to diagnose and are often confused with other native or alien taxa. Methods – The morphological characters of Atriplex, Oxybasis and Dysphania were reviewed using speci- mens from the herbaria B, BM, BR, BRLU, E, G, K, LE, MHA, MW, P, and W. Key results – A new species Atriplex congolensis Sukhor. is described from the highlands of D.R.Congo and illustrated. It was previously cited as A. hastata L. (now A. prostrata Boucher ex DC.) and is the only species of Atriplex sect. Teutliopsis Dumort. emend. Sukhor. in tropical Africa. A morphological comparison of all Atriplex representatives encountered in Africa (A. chenopodioides Batt., A. congolensis Sukhor., A. davisii Aellen, A. nilotica Sukhor., A. patula L., A. prostrata Boucher ex DC., and A. verreauxii Moq.) is provided. All records of the rare native Dysphania congolana (Hauman) Mosyakin & Clemants in mountainous tropical Africa are mapped using previously known and re-identified locations. -
A Synopsis of the Family Chenopodiaceae in India
Pleione 6(2): 273 - 297. 2012. ISSN: 0973-9467 © East Himalayan Society for Spermatophyte Taxonomy A synopsis of the Family Chenopodiaceae in India T. K. Paul Botanical Survey of India, Central National Herbarium, Howrah-711103, India E- mail: [email protected] Received revised 07.12.2012; Accepted 11.12.2012 Abstract The present paper presents a concise account of Chenopodiaceae in India. In all 19 genera with 50 species, 1 subspecies, 3 varieties have been recognized and another 2 genera and 14 species are cultivated or introduced. The genera and species are arranged in alphabetical order. Within the enumeration Key to genera and species, correct nomenclature, reference to type materials wherever available, phenology and distribution also have been added. Key words: India, Chenopodiaceae, Synopsis, comb. et stat. nov. INTRODUCTION The plants of Chenopodiaceae Ventenat, commonly known as ‘Goosefoot’ family, are mostly grow as weed and some are food plants like spinach, chard, beets, sugar beet and quinoa. The family is placed in the order Caryophyllales by Cronquist (1981), Takhtajan (1969) and Dahlgren (1975). Hutchinson (1959) and Thorne (1968, 1992) included the family in the order Chenopodiales, Ulbrich in Engler & Prantl (1934) in the order Centrospermae and Bentham & Hooker (1880) in the series Curvembryeae. Bentham & Hooker (1880) divided the family into two series, cyclobeae and spirolobeae. Cyclobeae is characterized by annular embryo, albumen copious whereas in spirolobeae the embryo is spiral and albumen scanty or absent. Williams & Ford-Lloyd (1974) recognised three subfamilies: Chenopodieae (embryo cyclical, operculum absent, endosperm absent, ovary superior), Salsoleae (embryo spiral, operculum absent, endosperm absent, ovary superior), Beteae (embryo cyclical, operculum present in fruit, endosperm present, ovary semi-inferior). -
Chenopodioideae, Chenopodiaceae/ Amaranthaceae): Implications for Evolution and Taxonomy
Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/ Amaranthaceae): Implications for Evolution and Taxonomy Alexander P. Sukhorukov1,2*, Mingli Zhang1,3 1 Key Laboratory of Biogeography and Bioresource in Arid Land, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi, Xinjiang, China, 2 Department of Higher Plants, Biological Faculty, Moscow Lomonosov State University, Moscow, Russia, 3 Institute of Botany, Chinese Academy of Sciences, Beijing, China Abstract A comparative carpological study of 96 species of all clades formerly considered as the tribe Chenopodieae has been conducted for the first time. The results show important differences in the anatomical structure of the pericarp and seed coat between representatives of terminal clades including Chenopodium s.str.+Chenopodiastrum and the recently recognized genera Blitum, Oxybasis and Dysphania. Within Chenopodium the most significant changes in fruit and seed structure are found in members of C. sect. Skottsbergia. The genera Rhagodia and Einadia differ insignificantly from Chenopodium. The evolution of heterospermy in Chenopodium is discussed. Almost all representatives of the tribe Dysphanieae are clearly separated from other Chenopodioideae on the basis of a diverse set of characteristics, including the small dimensions of the fruits (especially in Australian taxa), their subglobose shape (excl. Teloxys and Suckleya), and peculiarities of the pericarp indumentum. The set of fruit and seed characters evolved within the subfamily Chenopodioideae is described. A recent phylogenetic hypothesis is employed to examine the evolution of three (out of a total of 21) characters, namely seed color, testa-cell protoplast characteristics and embryo orientation. Citation: Sukhorukov AP, Zhang M (2013) Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/Amaranthaceae): Implications for Evolution and Taxonomy. -
WOOD ANATOMY of CHENOPODIACEAE (AMARANTHACEAE S
IAWA Journal, Vol. 33 (2), 2012: 205–232 WOOD ANATOMY OF CHENOPODIACEAE (AMARANTHACEAE s. l.) Heike Heklau1, Peter Gasson2, Fritz Schweingruber3 and Pieter Baas4 SUMMARY The wood anatomy of the Chenopodiaceae is distinctive and fairly uni- form. The secondary xylem is characterised by relatively narrow vessels (<100 µm) with mostly minute pits (<4 µm), and extremely narrow ves- sels (<10 µm intergrading with vascular tracheids in addition to “normal” vessels), short vessel elements (<270 µm), successive cambia, included phloem, thick-walled or very thick-walled fibres, which are short (<470 µm), and abundant calcium oxalate crystals. Rays are mainly observed in the tribes Atripliceae, Beteae, Camphorosmeae, Chenopodieae, Hab- litzieae and Salsoleae, while many Chenopodiaceae are rayless. The Chenopodiaceae differ from the more tropical and subtropical Amaran- thaceae s.str. especially in their shorter libriform fibres and narrower vessels. Contrary to the accepted view that the subfamily Polycnemoideae lacks anomalous thickening, we found irregular successive cambia and included phloem. They are limited to long-lived roots and stem borne roots of perennials (Nitrophila mohavensis) and to a hemicryptophyte (Polycnemum fontanesii). The Chenopodiaceae often grow in extreme habitats, and this is reflected by their wood anatomy. Among the annual species, halophytes have narrower vessels than xeric species of steppes and prairies, and than species of nitrophile ruderal sites. Key words: Chenopodiaceae, Amaranthaceae s.l., included phloem, suc- cessive cambia, anomalous secondary thickening, vessel diameter, vessel element length, ecological adaptations, xerophytes, halophytes. INTRODUCTION The Chenopodiaceae in the order Caryophyllales include annual or perennial herbs, sub- shrubs, shrubs, small trees (Haloxylon ammodendron, Suaeda monoica) and climbers (Hablitzia, Holmbergia). -
The C4 Plant Lineages of Planet Earth
Journal of Experimental Botany, Vol. 62, No. 9, pp. 3155–3169, 2011 doi:10.1093/jxb/err048 Advance Access publication 16 March, 2011 REVIEW PAPER The C4 plant lineages of planet Earth Rowan F. Sage1,*, Pascal-Antoine Christin2 and Erika J. Edwards2 1 Department of Ecology and Evolutionary Biology, The University of Toronto, 25 Willcocks Street, Toronto, Ontario M5S3B2 Canada 2 Department of Ecology and Evolutionary Biology, Brown University, 80 Waterman St., Providence, RI 02912, USA * To whom correspondence should be addressed. E-mail: [email protected] Received 30 November 2010; Revised 1 February 2011; Accepted 2 February 2011 Abstract Using isotopic screens, phylogenetic assessments, and 45 years of physiological data, it is now possible to identify most of the evolutionary lineages expressing the C4 photosynthetic pathway. Here, 62 recognizable lineages of C4 photosynthesis are listed. Thirty-six lineages (60%) occur in the eudicots. Monocots account for 26 lineages, with a Downloaded from minimum of 18 lineages being present in the grass family and six in the sedge family. Species exhibiting the C3–C4 intermediate type of photosynthesis correspond to 21 lineages. Of these, 9 are not immediately associated with any C4 lineage, indicating that they did not share common C3–C4 ancestors with C4 species and are instead an independent line. The geographic centre of origin for 47 of the lineages could be estimated. These centres tend to jxb.oxfordjournals.org cluster in areas corresponding to what are now arid to semi-arid regions of southwestern North America, south- central South America, central Asia, northeastern and southern Africa, and inland Australia. -
Vascular Plants of Santa Cruz County, California
ANNOTATED CHECKLIST of the VASCULAR PLANTS of SANTA CRUZ COUNTY, CALIFORNIA SECOND EDITION Dylan Neubauer Artwork by Tim Hyland & Maps by Ben Pease CALIFORNIA NATIVE PLANT SOCIETY, SANTA CRUZ COUNTY CHAPTER Copyright © 2013 by Dylan Neubauer All rights reserved. No part of this publication may be reproduced without written permission from the author. Design & Production by Dylan Neubauer Artwork by Tim Hyland Maps by Ben Pease, Pease Press Cartography (peasepress.com) Cover photos (Eschscholzia californica & Big Willow Gulch, Swanton) by Dylan Neubauer California Native Plant Society Santa Cruz County Chapter P.O. Box 1622 Santa Cruz, CA 95061 To order, please go to www.cruzcps.org For other correspondence, write to Dylan Neubauer [email protected] ISBN: 978-0-615-85493-9 Printed on recycled paper by Community Printers, Santa Cruz, CA For Tim Forsell, who appreciates the tiny ones ... Nobody sees a flower, really— it is so small— we haven’t time, and to see takes time, like to have a friend takes time. —GEORGIA O’KEEFFE CONTENTS ~ u Acknowledgments / 1 u Santa Cruz County Map / 2–3 u Introduction / 4 u Checklist Conventions / 8 u Floristic Regions Map / 12 u Checklist Format, Checklist Symbols, & Region Codes / 13 u Checklist Lycophytes / 14 Ferns / 14 Gymnosperms / 15 Nymphaeales / 16 Magnoliids / 16 Ceratophyllales / 16 Eudicots / 16 Monocots / 61 u Appendices 1. Listed Taxa / 76 2. Endemic Taxa / 78 3. Taxa Extirpated in County / 79 4. Taxa Not Currently Recognized / 80 5. Undescribed Taxa / 82 6. Most Invasive Non-native Taxa / 83 7. Rejected Taxa / 84 8. Notes / 86 u References / 152 u Index to Families & Genera / 154 u Floristic Regions Map with USGS Quad Overlay / 166 “True science teaches, above all, to doubt and be ignorant.” —MIGUEL DE UNAMUNO 1 ~ACKNOWLEDGMENTS ~ ANY THANKS TO THE GENEROUS DONORS without whom this publication would not M have been possible—and to the numerous individuals, organizations, insti- tutions, and agencies that so willingly gave of their time and expertise.