An Investigation Into Some Engineering Properties of Dracaena Arborea Nuts R
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Flavonoids and Stilbenoids of the Genera Dracaena and Sansevieria: Structures and Bioactivities
molecules Review Flavonoids and Stilbenoids of the Genera Dracaena and Sansevieria: Structures and Bioactivities Zaw Min Thu 1,* , Ko Ko Myo 1, Hnin Thanda Aung 2, Chabaco Armijos 3,* and Giovanni Vidari 4,* 1 Department of Chemistry, Kalay University, Kalay 03044, Sagaing Region, Myanmar; [email protected] 2 Department of Chemistry, University of Mandalay, Mandalay 100103, Myanmar; [email protected] 3 Departamento de Química y Ciencias Exactas, Universidad Técnica Particular de Loja, San Cayetano Alto s/n, Loja 1101608, Ecuador 4 Medical Analysis Department, Faculty of Science, Tishk International University, Erbil 44001, Iraq * Correspondence: [email protected] (Z.M.T.); [email protected] (C.A.); [email protected] (G.V.) Received: 18 May 2020; Accepted: 2 June 2020; Published: 3 June 2020 Abstract: The genera Dracaena and Sansevieria (Asparagaceae, Nolinoideae) are still poorly resolved phylogenetically. Plants of these genera are commonly distributed in Africa, China, Southeast Asia, and America. Most of them are cultivated for ornamental and medicinal purposes and are used in various traditional medicines due to the wide range of ethnopharmacological properties. Extensive in vivo and in vitro tests have been carried out to prove the ethnopharmacological claims and other bioactivities. These investigations have been accompanied by the isolation and identification of hundreds of phytochemical constituents. The most characteristic metabolites are steroids, flavonoids, stilbenes, and saponins; many of them exhibit potent analgesic, anti-inflammatory, antimicrobial, antioxidant, antiproliferative, and cytotoxic activities. This review highlights the structures and bioactivities of flavonoids and stilbenoids isolated from Dracaena and Sansevieria. Keywords: Dracaena; Sansevieria; biological/pharmacological activities; flavonoids; stilbenoids 1. Introduction The taxonomic boundaries of the dracaenoid genera Dracaena and Sansevieria have long been debated. -
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 -
Complete Chloroplast Genomes Shed Light on Phylogenetic
www.nature.com/scientificreports OPEN Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Ju Namgung1,4, Hoang Dang Khoa Do1,2,4, Changkyun Kim1, Hyeok Jae Choi3 & Joo‑Hwan Kim1* Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, fve of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein‑coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA , psbA upstream, rpl32- trnL-UAG , ycf1, rpl22, matK, and ndhF, were identifed in the studied Allium species. Additionally, we present the frst phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, fve species of Amaryllidoideae, one species of Agapanthoideae, and fve species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae‑Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae‑ Gilliesieae‑Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by diferentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya. -
List 01 Hawaiian Names 01 Plants
V\.{). 3 v BOTANICAL BULLETIN NO.2 JUNE. 1913 TERRITORY OF HAWAII BOARD OF AGRICULTURE AND FORESTRY List 01 Hawaiian Names 01 Plants BY JOSEPH F. ROCK Consulting Botanist, Board of Agriculture and Forestry HONOLULU: HAWAIIAN GAZETTE CO., LTD. 1913 ALPHABETICAL LIST OF HAWAIIAN NAMES OF PLANTS. The following list of Hawaiian plant-names has been compiled from various sources. Hillebrand in his valuable Flora of the Hawaiian Islands has given many Hawaiian names, especially of the more common species; these are incorporated in this list with a few corrections. Nearly all Hawaiian plant-names found in this list and not in Hillebrand's Flora were secured from Mr. Francis Gay of the Island of Kauai, an old resident in this Terri tory and well acquainted with its plants from a layman's stand point. It was the writer's privilege to camp with Mr. Gay in the mountains of Kauai collecting botanical material; for almost every species he could give the native name, which he had se cured in the early days from old and reliable natives. Mr. Gay had made spatter prints of many of the native plants in a large record book with their names and uses, as well as their symbolic meaning when occurring in mele (songs) or olioli (chants), at tached to them. For all this information the writer is indebted mainly to Mr. Francis Gay and also to Mr. Augustus F. Knudsen of the same Island. The writer also secured Hawaiian names from old na tives and Kahunas (priests) in the various islands of the group. -
Dyuhei Sato Division of Genetics, Bot. Inst. Faculty of Science, Tokyo
ANALYSIS OF THE KARYOTYPES IN YUCCA, A GA VE AND THE RELATED GENERA WITH SPECIAL REFERENCE TO THE PHYLOGENETIC SIGNIFICANCEI~ Dyuhei SATo Divisionof Genetics, Bot. Inst. Faculty of Science, Tokyo Imperial University McKelvey and Sax (2933) have called attention to the existence of taxonomic and cytological similarities of the genera Yucca, Hesperoyucca, Gleistvucca,Hesperoaloe and Samuela of the Liliaceae with the genera Agave and Fourcroya which belong to a related family, Amaryllidaceae. Wh.itaker (1934) also has reported that Polianhes and Fourcroya have exactly the same chromosome constitution as the Yucca-Abave karyotype (5 long and 25 short chromosomes) (Figs. 1, 2). These observations when considered in respect to taxonomic resemblances, seem to indicate that the genera mentioned above are more closely related than it is shown by their classifica- tion into distinct families. Whitaker also has remarked that Dasylirion (2n=38) and ATolina(2n=36) in Yucceae and Doryanthes (2n=36) in Agavoideae are of different karyotypes from the Yucca-Agave type. In the present work an analysis of the karyotypes in Liliaceous plants has been attempted and several karyotypes have been found in Scilloideae. Eucornis and Carassia have been selected with the purpose of discovering a possible connecting link between these genera and the Yucca-Agave group. In the present paper an analysis of the karyotypes of the following species is given. LILIACEAE Scilloideae 211 Fig. Euconis undulata 60=8L+8M+44S (4b)2) 3 Euconsispallidi ora 60=8L+8M+44S (4b) 4 Eucomispunctata 60=8L±8M+44S (4b) 5 Camassiaescrema 30=6L+24S (2b) 6 Yucceae Yuccafilamentosa 30 60=1OL+50S (2b) 1, 7 Yuccarecurvifolia 30 60=1OL+50S (2b) 2, 8 Yuccaaloifolia 60=1OL+50S (2b) 9 „ var. -
Massonia Amoena (Asparagaceae, Scilloideae), a Striking New Species from the Eastern Cape, South Africa
Phytotaxa 181 (3): 121–137 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.181.3.1 Massonia amoena (Asparagaceae, Scilloideae), a striking new species from the Eastern Cape, South Africa MARIO MARTÍNEZ-AZORÍN1,2, MICHAEL PINTER1, GERFRIED DEUTSCH1, ANDREAS BRUDERMANN1, ANTHONY P. DOLD3, MANUEL B. CRESPO2, MARTIN PFOSSER4 & WOLFGANG WETSCHNIG1* 1Institute of Plant Sciences, NAWI Graz, Karl-Franzens-University Graz, Holteigasse 6, A-8010 Graz, Austria; e-mail: wolfgang.wet- [email protected] 2CIBIO (Instituto Universitario de la Biodiversidad), Universidad de Alicante, P. O. Box 99, E-03080 Alicante, Spain. 3Selmar Schonland Herbarium, Department of Botany, Rhodes University, Grahamstown 6140 South Africa. 4Biocenter Linz, J.-W.-Klein-Str. 73, A-4040 Linz, Austria. *author for correspondence Abstract As part of an ongoing study towards a taxonomic revision of the genus Massonia Houtt., a new species, Massonia amoena Mart.-Azorín, M.Pinter & Wetschnig, is here described from the Eastern Cape Province of South Africa. This new species is characterized by the leaves bearing heterogeneous circular to elongate pustules and the strongly reflexed perigone seg- ments at anthesis. It is at first sight related to Massonia jasminiflora Burch. ex Baker, M. wittebergensis U.Müll.-Doblies & D.Müll.-Doblies and M. saniensis Wetschnig, Mart.-Azorín & M.Pinter, but differs in vegetative and floral characters, as well as in its allopatric distribution. A complete morphological description of the new species and data on biology, habitat, and distribution are presented. Key words: flora, Hyacinthaceae, Massonieae, Southern Africa, taxonomy Introduction Hyacinthaceae sensu APG (2003) includes ca. -
Agave Americana and Furcraea Andina: Key Species to Andean Cultures in Ecuador
Ethnobotany Agave americana and Furcraea andina: Key Species to Andean Cultures in Ecuador LUCÍA DE LA TORRE1*, IAN CUMMINS2, AND ELIOT LOGAN-HINES2 Botanical Sciences 96 (2): 246-266, 2018 Abstract Background: The rich Agaveae-based culture that exists in the Ecuadorian Andes is little known. Wild DOI: 10.17129/botsci.1813 and cultivated rosettes of Agave americana and Furcraea andina coexist in arid Andean landscapes. A. americana is considered an introduced species to Ecuador. Received: Questions: What are Agaveae use patterns and cultural importance in the Ecuadorian Andes? Is the ethno- December 19th, 2017 Accepted: botanical significance of Agave in Ecuador comparable to that in Mexico and other Andean countries? Agave americana, Furcraea andina March 12th, 2018 Species studied: Associated editor: Study site, dates: Ecuadorian Andes, 2016. Salvadro Arias Methods: Semi-structured interviews to Agaveae users (37) and a review of literature on ethnobotanical research conducted in Ecuador since the 18th century. Results: A. americana is more diversely and widely used than F. andina (124 vs 36 uses and 548 vs 140 use records, respectively). The versatility of A. americana lies in its mishki (sap extracted from its heart) which has multiple medicinal, edible and ceremonial applications. We found significant variation of its use patterns throughout the region. The main use of F. andina as a source of fiber is disappearing. Most productive initiatives involve A. americana (92 %, n = 53). Conclusion: The importance of A. americana in the Ecuadorian Andes is comparable to that of agaves in Mexico, but not to its importance in other Andean countries where it is used sporadically. -
Mini Data Sheet on Asparagus Asparagoides (Asparagaceae)
EPPO, 2013 Mini data sheet on Asparagus asparagoides (Asparagaceae) Added in 2012 – Deleted in 2013 Reasons for deletion: Asparagus asparagoides was added to the EPPO Alert List in 2012 but as no immediate risk was perceived, it was transferred to the Observation List in 2013. Why Asparagus asparagoides (Asparagaceae) is a rhizomatous perennial climbing vine originating from South Africa. One of its English common names is “bridal creeper”. This species is invasive in Australia. It is used as an ornamental plant in the EPPO region, and is listed as an invasive alien plant in Spain, but is also present in other EPPO member countries. Considering the invasive behavior of this species elsewhere in the world as well as in EPPO countries, it is considered that Mediterranean and Macaronesian countries may be at risk, and that the species should usefully be monitored. Geographical distribution EPPO region: France (including Corse), Italy (Sicilia), Malta, Morocco, Portugal (Azores, Madeira), Spain (including Islas Canarias), Tunisia. Note: The species had erroneously been indicated as present in Slovenia (from an incorrect interpretation of Jogan, 2005). Africa (native): Ethiopia, Kenya, Lesotho, Malawi, Morocco, Namibia, South Africa, Swaziland, Tanzania, Tunisia, Uganda, Zimbabwe. North America: Mexico, USA (California, Hawaii (East Maui)). South and Central America: Argentina, Guatemala, Uruguay. Oceania (invasive): Australia (New South Wales, Queensland, South Australia, Tasmania, Victoria, Western Australia), New Zealand. Morphology A. asparagoides is a geophyte with a perennial cylindrical, slender (about 5 mm wide), branching rhizome, growing parallel to the soil surface, bearing fleshy tubers (25–42 mm long and 8–20 mm wide). It produces thin shoots, slightly woody at the base and up to 6 m long when support is available. -
Two New Species and One New Variety of Aspidistra (Asparagaceae: Nolinoideae) from Southern Vietnam
Gardens’ Bulletin Singapore 66(1): 27–37. 2014 27 Two new species and one new variety of Aspidistra (Asparagaceae: Nolinoideae) from southern Vietnam 1 2 3 J. Leong-Škorničková , H.-J. Tillich & Q.B. Nguyễn 1Herbarium, Singapore Botanic Gardens, National Parks Board, 1 Cluny Road, Singapore 259569 [email protected] 2Ludwig-Maximilians-University, Systematic Botany, Menzinger Str. 67, D-80638 Munich, Germany [email protected] 3 Vietnam National Museum of Nature, Vietnam Academy of Science and Technology, 18 Hoàng Quốc Việt Street, Cầu Giấy, Hanoi, Vietnam ABSTRACT. Two new species and one new variety of Aspidistra Ker-Gawl. (Asparagaceae: Nolinoideae) from southern and central Vietnam, A. ventricosa Tillich & Škorničk., A. mirostigma Tillich & Škorničk., and A. connata Tillich var. radiata Tillich & Škorničk., are described and illustrated here. Keywords. Asparagaceae, Aspidistra, Convallariaceae s. str., Nolinoideae, Ruscaceae s.l., Vietnam Introduction The genus Aspidistra Ker-Gawl. (Asparagaceae: Nolinoideae – formerly also placed in Convallariaceae and in Ruscaceae) ranges from Assam (India) in the west to southern Japan in the east, and from central China southwards to the Malay Peninsula. Its centre of diversity is in southeast China (Guangxi Province) and adjacent northern Vietnam (Tillich, 2005). The number of known species continues to grow as the Indochinese floristic region is better explored. Currently more than 100 species are recognised (Tillich & Averyanov, 2012) of which many were first reported from Vietnam only in the last decade (Bogner & Arnautov, 2004; Bräuchler & Ngoc, 2005; Tillich, 2005, 2006, 2008; Tillich et al., 2007; Tillich & Averyanov, 2008, 2012; Averyanov & Tillich, 2012, 2013, submitted; Tillich & Leong-Škorničková, 2013; Vislobokov et al., 2013). -
Assessment of Photosynthetic Potential of Indoor Plants Under Cold Stress
DOI: 10.1007/s11099-015-0173-7 PHOTOSYNTHETICA 54 (1): 138-142, 2016 BRIEF COMMUNICATION Assessment of photosynthetic potential of indoor plants under cold stress S.M. GUPTA+, A. AGARWAL, B. DEV, K. KUMAR, O. PRAKASH, M.C. ARYA, and M. NASIM Molecular Biology and Genetic Engineering Laboratory, Defence Institute of Bio-Energy Research, Goraparao, P.O.-Arjunpur, Haldwani, Dist.-Nainital (UK) – 263 139, India Abstract Photosynthetic parameters including net photosynthetic rate (PN), transpiration rate (E), water-use efficiency (WUE), and stomatal conductance (gs) were studied in indoor C3 plants Philodendron domesticum (Pd), Dracaena fragans (Df), Peperomia obtussifolia (Po), Chlorophytum comosum (Cc), and in a CAM plant, Sansevieria trifasciata (St), exposed to various low temperatures (0, 5, 10, 15, 20, and 25C). All studied plants survived up to 0ºC, but only St and Cc endured, while other plants wilted, when the temperature increased back to room temperature (25C). The PN declined rapidly with –2 –1 the decrease of temperature in all studied plants. St showed the maximum PN of 11.9 mol m s at 25ºC followed by Cc, –2 –1 Po, Pd, and Df. E also followed a trend almost similar to that of PN. St showed minimum E (0.1 mmol m s ) as compared to other studied C3 plants at 25ºC. The E decreased up to ~4-fold at 5 and 0ºC. Furthermore, a considerable decline in WUE was observed under cold stress in all C3 plants, while St showed maximum WUE. Similarly, the gs also declined gradually with the decrease in the temperature in all plants. -
Austronea Patersoniae (Asparagaceae, Scilloideae), a New Species from the Eastern Cape Province in South Africa
Phyt otaxa 400 (2): 076-080 https://W\\ ''.m a press.com/j/pt/ Copyright © 2019 Magnolia Press Article https://doi.org/10. 11646/phytotaxa.400.2.4 Austronea patersoniae (Asparagaceae, Scilloideae), a new species from the Eastern Cape Province in South Africa MARIO MARTiNEZ-AZORfN'·, ANTHONY P. DOLD2 & MANUEL B. CRESP01 1D epto. de Ciencias Ambientales y Recursos aturales (dCARN), Universidad de Alicante, P. 0. Box 99, E-03080 Alicante, Spain: e-mail: [email protected] JSe/mar Schonland Herbarium, Department ofB otaff)\ Rhodes University. Grahamstown 61-10, South Africa. "author for correspondence Abstract Our fieldwork in the Eastern Cape province of South Africa revealed an undescribed species of Austronea which was named by Schonland as "Urginea Patersoniae Schonl. Ms.", but never validly published. We here describe Austronea patersoniae to include plants showing bulbs with loose scales; 5-9 narrowly linear erect leaves with papillate margins; elongate pe duncle; lowermost bracts with a broad, flat, papery spur and reddish flowers with papillate filaments. We provide a complete morphological description as well as data on ecology and distribution. Keywords: Distribution, ecology, Hyacinthaceae, taxonomy, Urgineoideae Introduction Austronea Mart.-Azorln, M.B.Crespo, M.Pinter & Wetschnig in Martinez-Azorln et al. (20 18a: I 05) has been recently described to include some species of Hyacinthaceae subfamily Urgineoideae (= Asparagaceae subfam. Scilloideae tribe Urgineeae) from southern Africa, which were traditionally included in Urginea -
No. 34 March 2016
No. 34 March 2016 Sansevieria 34/2016 pages 14 - 26 The Genus Sansevieria: An Introduction to Molecular (DNA) Analysis and Preliminary Insights to Intrageneric Relationships Andrew S. Baldwin*, Robert H. Webb** *Department of Life Science, Mesa Community College, Mesa, Arizona **School of Natural Resources, University of Arizona, Tucson, Arizona Contact: [email protected] All photos by the Author Summary species? So, in this article, pretend that the genus San- Molecular biology, particularly as it involves the analysis sevieria, and the use of molecular biology, is on trial and of DNA, is growing in importance within plant taxon- you are the jury: will you vote for conviction or acquittal? omy to resolve how families and genera are related and to even resolve plant species from one another. Here, we Biogeography review some of the concepts of molecular biology with As the readers of this journal are well aware, Sansevieria an emphasis on how it may help to unravel certain long- is a cosmopolitan genus that occurs in Africa, the Middle debated issues within the genus Sansevieria as well as the East, and the Asian subcontinent. The diversity in form placement of this genus among other related genera. We is rather astonishing, ranging from tiny little plants, provide some preliminary data and offer a few insights some with stout, spiky leaves and others with thin, flat but caution against jumping to any conclusions about ones, to formidable shrubs 2-4 m in height. What holds Sansevierias without considerable additional data. this group of plants together within the genus Sansevier- ia are the similar flowers and seeds, but some believe that Introduction the flowers and seeds aren’t so unique to exclude larger, A well-respected succulent plant and cactus collector related plants currently within the genus Dracaena (Bos, and researcher from England reportedly refers to DNA 1984), and some molecular data bear this out (Lu and as “Damned Nasty Answers” because he doesn’t particu- Morden, 2014).