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Tianma, Gastrodia Tuber)
Chapter 13 Gastrodia elata Blume. 天麻 (Tianma, Gastrodia Tuber) Hui-Min Gao 13.1 Botanical Identity Tianma, the steamed and dried rhizome of Gastrodia elata Blume. (Orchid Family), is one of the most popular traditional Chinese medicines and a famous foodstuff in China. It was first recorded in Shen-nung-pen-tsao-ching as a high-grade drug and widely used for the treatment of headache, dizziness, vertigo, convulsion, hyper- tension and other neurodegenerative diseases [1]. The orchid G. elata, lacking green leaves and chlorophyll, is a saprophytic perennial herb and it grows in the glades or at the edge of forests in humid mountain areas with the altitude of 400– 3200 m. This species lives in symbiotic association with the honey mushroom (Armillariella mellea) and its whole growth cycle except for florescence, is in the underground [2]. The wild G. elata distributed in China’s southwest, northeast and central regions, and especially, the rhizomes collected in the western Guizhou, southern Sichuan and northeastern Yunnan are considered to be the genuine medicinal material with good prestige. Due to the increasing market demand, natural reserves of G. elata have drastically decreased and the species has been listed as rare and endangered one in China and even around the world. Since the 1970s, G. elata has been extensively cultivated in Shaanxi, Anhui, Sichuan, Guizhou and Yunnan, and to date, Lueyang in Shaanxi province, has become the biggest production base all over the country. The rhizome is harvested from early winter to late spring, washed clean imme- diately, steamed thoroughly, spread out and dried at a lower temperature. -
Chromosomal Evolution and Apomixis in the Cruciferous Tribe Boechereae
fpls-11-00514 May 26, 2020 Time: 17:57 # 1 ORIGINAL RESEARCH published: 28 May 2020 doi: 10.3389/fpls.2020.00514 Chromosomal Evolution and Apomixis in the Cruciferous Tribe Boechereae Terezie Mandáková1, Petra Hloušková1, Michael D. Windham2, Thomas Mitchell-Olds2, Kaylynn Ashby3, Bo Price3, John Carman3 and Martin A. Lysak1* 1 CEITEC, Masaryk University, Brno, Czechia, 2 Department of Biology, Duke University, Durham, NC, United States, 3 Plants, Soils, and Climate Department, Utah State University, Logan, UT, United States The mustard family (Brassicaceae) comprises several dozen monophyletic clades usually ranked as tribes. The tribe Boechereae plays a prominent role in plant research due to the incidence of apomixis and its close relationship to Arabidopsis. This tribe, largely confined to western North America, harbors nine genera and c. 130 species, with >90% of species belonging to the genus Boechera. Hundreds of apomictic diploid and triploid Boechera hybrids have spurred interest in this genus, but the remaining Boechereae genomes remain virtually unstudied. Here we report on comparative Edited by: genome structure of six genera (Borodinia, Cusickiella, Phoenicaulis, Polyctenium, Steven Dodsworth, Nevada, and Sandbergia) and three Boechera species as revealed by comparative University of Bedfordshire, United Kingdom chromosome painting (CCP). All analyzed taxa shared the same seven-chromosome Reviewed by: genome structure. Comparisons with the sister Halimolobeae tribe (n = 8) showed Ana Paula Moraes, that the ancestral Boechereae genome (n = 7) was derived from an older n = 8 Universidade Federal do ABC, Brazil Aretuza Sousa Dos Santos, genome by descending dysploidy followed by the divergence of extant Boechereae Ludwig Maximilian University taxa. -
Apiales, Aquifoliales, Boraginales, , Brassicales, Canellales
Kingdom: Plantae Phylum: Tracheophyta Class: Magnoliopsida Order: Apiales, Aquifoliales, Boraginales, , Brassicales, Canellales, Caryophyllales, Celastrales, Ericales, Fabales, Garryales, Gentianales, Lamiales, Laurales, Magnoliales, Malpighiales, Malvales, Myrtales, Oxalidales, Picramniales, Piperales, Proteales, Rosales, Santalales, Sapindales, Solanales Family: Achariaceae, Anacardiaceae, Annonaceae, Apocynaceae, Aquifoliaceae, Araliaceae, Bignoniaceae, Bixaceae, Boraginaceae, Burseraceae, Calophyllaceae, Canellaceae, Cannabaceae, Capparaceae, Cardiopteridaceae, Caricaceae, Caryocaraceae, Celastraceae, Chrysobalanaceae, Clusiaceae, Combretaceae, Dichapetalaceae, Ebenaceae, Elaeocarpaceae, Emmotaceae, Erythroxylaceae, Euphorbiaceae, Fabaceae, Goupiaceae, Hernandiaceae, Humiriaceae, Hypericaceae, Icacinaceae, Ixonanthaceae, Lacistemataceae, Lamiaceae, Lauraceae, Lecythidaceae, Lepidobotryaceae, Linaceae, Loganiaceae, Lythraceae, Malpighiaceae, Malvaceae, Melastomataceae, Meliaceae, Monimiaceae, Moraceae, Myristicaceae, Myrtaceae, Nyctaginaceae, Ochnaceae, Olacaceae, Oleaceae, Opiliaceae, Pentaphylacaceae, Phyllanthaceae, Picramniaceae, Piperaceae, Polygonaceae, Primulaceae, Proteaceae, Putranjivaceae, Rhabdodendraceae, Rhamnaceae, Rhizophoraceae, Rosaceae, Rubiaceae, Rutaceae, Sabiaceae, Salicaceae, Sapindaceae, Sapotaceae, Simaroubaceae, Siparunaceae, Solanaceae, Stemonuraceae, Styracaceae, Symplocaceae, Ulmaceae, Urticaceae, Verbenaceae, Violaceae, Vochysiaceae Genus: Abarema, Acioa, Acosmium, Agonandra, Aiouea, Albizia, Alchornea, -
Endosamara Racemosa (Roxb.) Geesink and Callerya Vasta (Kosterm.) Schot
Taiwania, 48(2): 118-128, 2003 Two New Members of the Callerya Group (Fabaceae) Based on Phylogenetic Analysis of rbcL Sequences: Endosamara racemosa (Roxb.) Geesink and Callerya vasta (Kosterm.) Schot (1,3) (1,2) Jer-Ming Hu and Shih-Pai Chang (Manuscript received 2 May, 2003; accepted 29 May, 2003) ABSTRACT: Two new members of Callerya group in Fabaceae, Endosamara racemosa (Roxb.) Geesink and Callerya vasta (Kosterm.) Schot, are identified based on phylogenetic analyses of chloroplast rbcL sequences. These taxa joined with other previously identified taxa in the Callerya group: Afgekia, Callerya, and Wisteria. These genera are resolved as a basal subclade in the Inverted Repeat Lacking Clade (IRLC), which is a large legume group that includes many temperate and herbaceous legumes in the subfamily Papilionoideae, such as Astragalus, Medicago and Pisum, and is not close to other Millettieae. Endosamara is sister to Millettia japonica (Siebold & Zucc.) A. Gray, but only weakly linked with Wisteria and Afgekia. KEY WORDS: Endosamara, Callerya, Millettieae, Millettia, rbcL, Phylogenetic analysis. INTRODUCTION Recent molecular phylogenetic studies of the tribe Millettieae have revealed that the tribe is polyphyletic and several taxa are needed to be segregated from the core Millettieae group. One of the major segregates from Millettieae is the Callerya group, comprising species from Callerya, Wisteria, Afgekia, and Millettia japonica (Siebold & Zucc.) A. Gray. The group is considered to be part of the Inverted-Repeat-Lacking Clade (IRLC; Wojciechowski et al., 1999) including many temperate herbaceous legumes. Such result is consistent and supported by chloroplast inverted repeat surveys (Lavin et al., 1990; Liston, 1995) and phylogenetic studies of the phytochrome gene family (Lavin et al., 1998), chloroplast rbcL (Doyle et al., 1997; Kajita et al., 2001), trnK/matK (Hu et al., 2000), and nuclear ribosomal ITS regions (Hu et al., 2002). -
Gastrodia Bambu (Orchidaceae: Epidendroideae), a New Species from Java, Indonesia
Phytotaxa 317 (3): 211–218 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.317.3.5 Gastrodia bambu (Orchidaceae: Epidendroideae), A New Species from Java, Indonesia DESTARIO METUSALA1,2 & JATNA SUPRIATNA2 1Purwodadi Botanic Garden, Indonesian Institute of Sciences (LIPI), Jl. Raya Surabaya-Malang km.65, Pasuruan, East Java, Indone- sia; Email: [email protected] 2Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Indonesia. Abstract Gastrodia bambu Metusala, a new species of Gastrodia (Orchidaceae: Epidendroideae, Gastrodieae) from Mount Merapi, Yogyakarta Province, Java, Indonesia, is described and illustrated. This new species is morphologically close to Gastrodia abscondita J.J.Sm, but differs in having a larger dark brown flower, a longer perianth tube, ovate petals, a longer and oblong- lanceolate lip, a different shape keels on lip, and a different shape column. Key words: Gastrodia, Java, Mount Merapi, holomycotrophic Introduction The genus Gastrodia R.Br (Brown 1810: 330) (Orchidaceae: Epidendroideae) is a genus of holomycotrophic terrestrial orchids that consists of approximately 80 accepted names, most of them being endemic species (Govaerts et al. 2017). This genus is characterized by having an underground fleshy rhizome, lacking functional leaves and chlorophyll, with sepals and petals connate into a 5-lobed tube, and having two mealy pollinia that lack caudicles (Seidenfaden & Wood 1992; Pridgeon et al. 2005; Cribb et al. 2010). It is widely distributed from northeastern India across southern China to Japan, eastern Siberia, the Southeast Asia, Australia, New Guinea, Solomon islands, and westwards to Madagascar, Mascarene Islands and tropical Africa (Pridgeon et al. -
Supplemental Information.Pdf
SUPPORTING INFORMATION Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the Cretaceous-Paleogene boundary Kevin Vanneste1,2, Guy Baele3, Steven Maere1,2,*, and Yves Van de Peer1,2,4,* 1 Department of Plant Systems Biology, VIB, Ghent, Belgium 2 Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium 3 Department of Microbiology and Immunology, Rega Institute, KU Leuven, Leuven, Belgium 4 Department of Genetics, Genomics Research Institute, University of Pretoria, Pretoria, South Africa *Corresponding authors Yves Van de Peer Steven Maere VIB / Ghent University VIB / Ghent University Technologiepark 927 Technologiepark 927 Gent (9052), Belgium Gent (9052), Belgium Tel: +32 (0)9 331 3807 Tel: +32 (0)9 331 3805 Fax: +32 (0)9 331 3809 Fax: +32 (0)9 331 3809 E-mail: [email protected] E-mail: [email protected] Overview Species grouping topology ................................................ 3 Calibrations and constraints .............................................. 5 Alternative calibrations and constraints ............................ 13 Relative rate tests ............................................................. 27 Re-dating the Pyrus bretschneideri WGD ......................... 30 WGD age estimates from literature ................................... 33 Eschscholzia californica and Acorus americanus ............. 34 2 Species grouping topology In order to date the node joining the homeologous pair, orthogroups were constructed consisting of both homeologs and orthologs from other plant species for which full genome sequence information was available. Different plant species were grouped into ‘species groups’ for which one ortholog was selected and added to the orthogroup, in order to keep the orthogroup topology fixed and to facilitate automation on the one hand, but also to allow enough orthogroups to be constructed on the other hand (see Material and methods). -
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 -
Arthur Monrad Johnson Colletion of Botanical Drawings
http://oac.cdlib.org/findaid/ark:/13030/kt7489r5rb No online items Arthur Monrad Johnson colletion of botanical drawings 1914-1941 Processed by Pat L. Walter. Louise M. Darling Biomedical Library History and Special Collections Division History and Special Collections Division UCLA 12-077 Center for Health Sciences Box 951798 Los Angeles, CA 90095-1798 Phone: 310/825-6940 Fax: 310/825-0465 Email: [email protected] URL: http://www.library.ucla.edu/libraries/biomed/his/ ©2008 The Regents of the University of California. All rights reserved. Arthur Monrad Johnson colletion 48 1 of botanical drawings 1914-1941 Descriptive Summary Title: Arthur Monrad Johnson colletion of botanical drawings, Date (inclusive): 1914-1941 Collection number: 48 Creator: Johnson, Arthur Monrad 1878-1943 Extent: 3 boxes (2.5 linear feet) Repository: University of California, Los Angeles. Library. Louise M. Darling Biomedical Library History and Special Collections Division Los Angeles, California 90095-1490 Abstract: Approximately 1000 botanical drawings, most in pen and black ink on paper, of the structural parts of angiosperms and some gymnosperms, by Arthur Monrad Johnson. Many of the illustrations have been published in the author's scientific publications, such as his "Taxonomy of the Flowering Plants" and articles on the genus Saxifraga. Dr. Johnson was both a respected botanist and an accomplished artist beyond his botanical subjects. Physical location: Collection stored off-site (Southern Regional Library Facility): Advance notice required for access. Language of Material: Collection materials in English Preferred Citation [Identification of item], Arthur Monrad Johnson colletion of botanical drawings (Manuscript collection 48). Louise M. Darling Biomedical Library History and Special Collections Division, University of California, Los Angeles. -
Lessons from 20 Years of Plant Genome Sequencing: an Unprecedented Resource in Need of More Diverse Representation
bioRxiv preprint doi: https://doi.org/10.1101/2021.05.31.446451; this version posted May 31, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Lessons from 20 years of plant genome sequencing: an unprecedented resource in need of more diverse representation Authors: Rose A. Marks1,2,3, Scott Hotaling4, Paul B. Frandsen5,6, and Robert VanBuren1,2 1. Department of Horticulture, Michigan State University, East Lansing, MI 48824, USA 2. Plant Resilience Institute, Michigan State University, East Lansing, MI 48824, USA 3. Department of Molecular and Cell Biology, University of Cape Town, Rondebosch 7701, South Africa 4. School of Biological Sciences, Washington State University, Pullman, WA, USA 5. Department of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, USA 6. Data Science Lab, Smithsonian Institution, Washington, DC, USA Keywords: plants, embryophytes, genomics, colonialism, broadening participation Correspondence: Rose A. Marks, Department of Horticulture, Michigan State University, East Lansing, MI 48824, USA; Email: [email protected]; Phone: (603) 852-3190; ORCID iD: https://orcid.org/0000-0001-7102-5959 Abstract The field of plant genomics has grown rapidly in the past 20 years, leading to dramatic increases in both the quantity and quality of publicly available genomic resources. With an ever- expanding wealth of genomic data from an increasingly diverse set of taxa, unprecedented potential exists to better understand the evolution and genome biology of plants. -
Taxa Named in Honor of Ihsan A. Al-Shehbaz
TAXA NAMED IN HONOR OF IHSAN A. AL-SHEHBAZ 1. Tribe Shehbazieae D. A. German, Turczaninowia 17(4): 22. 2014. 2. Shehbazia D. A. German, Turczaninowia 17(4): 20. 2014. 3. Shehbazia tibetica (Maxim.) D. A. German, Turczaninowia 17(4): 20. 2014. 4. Astragalus shehbazii Zarre & Podlech, Feddes Repert. 116: 70. 2005. 5. Bornmuellerantha alshehbaziana Dönmez & Mutlu, Novon 20: 265. 2010. 6. Centaurea shahbazii Ranjbar & Negaresh, Edinb. J. Bot. 71: 1. 2014. 7. Draba alshehbazii Klimeš & D. A. German, Bot. J. Linn. Soc. 158: 750. 2008. 8. Ferula shehbaziana S. A. Ahmad, Harvard Pap. Bot. 18: 99. 2013. 9. Matthiola shehbazii Ranjbar & Karami, Nordic J. Bot. doi: 10.1111/j.1756-1051.2013.00326.x, 10. Plocama alshehbazii F. O. Khass., D. Khamr., U. Khuzh. & Achilova, Stapfia 101: 25. 2014. 11. Alshehbazia Salariato & Zuloaga, Kew Bulletin …….. 2015 12. Alshehbzia hauthalii (Gilg & Muschl.) Salariato & Zuloaga 13. Ihsanalshehbazia Tahir Ali & Thines, Taxon 65: 93. 2016. 14. Ihsanalshehbazia granatensis (Boiss. & Reuter) Tahir Ali & Thines, Taxon 65. 93. 2016. 15. Aubrieta alshehbazii Dönmez, Uǧurlu & M.A.Koch, Phytotaxa 299. 104. 2017. 16. Silene shehbazii S.A.Ahmad, Novon 25: 131. 2017. PUBLICATIONS OF IHSAN A. AL-SHEHBAZ 1973 1. Al-Shehbaz, I. A. 1973. The biosystematics of the genus Thelypodium (Cruciferae). Contrib. Gray Herb. 204: 3-148. 1977 2. Al-Shehbaz, I. A. 1977. Protogyny, Cruciferae. Syst. Bot. 2: 327-333. 3. A. R. Al-Mayah & I. A. Al-Shehbaz. 1977. Chromosome numbers for some Leguminosae from Iraq. Bot. Notiser 130: 437-440. 1978 4. Al-Shehbaz, I. A. 1978. Chromosome number reports, certain Cruciferae from Iraq. -
Diploid Apomicts of the Boechera Holboellii Complex Display Large-Scale Chromosome Substitutions and Aberrant Chromosomes
Diploid apomicts of the Boechera holboellii complex display large-scale chromosome substitutions and aberrant chromosomes Laksana Kantama*†, Timothy F. Sharbel‡, M. Eric Schranz§, Thomas Mitchell-Olds¶, Sacco de Vries*, and Hans de Jongʈ** *Laboratory of Biochemistry, Wageningen University, Dreijenlaan 3, NL-6703 HA, Wageningen, The Netherlands; ‡Apomixis Research Group, Department of Cytogenetics and Genome Analysis, Leibniz Institute of Plant Genetics and Crop Plant Research, D-06466 Gatersleben, Germany; §Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Kruislaan 318, NL-1098 MS, Amsterdam, The Netherlands; ¶Department of Biology, Duke University, Durham, NC 27708; and ʈLaboratory of Genetics, Wageningen University, Arboretumlaan 4, NL-6703 BD, Wageningen, The Netherlands Communicated by Maarten Koornneef, Wageningen University and Research Centre, Wageningen, The Netherlands, July 15, 2007 (received for review May 20, 2007) We conducted a cytogenetic study of sexual lines of Boechera holboellii is polyphyletic. Its sequence and microsatellite analyses and seven diploid apomic- have shown that B. divaricarpa arose through hybridization (14 ؍ stricta and Boechera holboellii (2n tic accessions of their interspecific hybrid Boechera divaricarpa and between sexual B. stricta and B. holboellii or a closely related or 15). By studying chromosome morphology, species (3, 5, 6). The level of allelic variation is comparable 14 ؍ B. holboellii (2n rDNA repeats, genome painting, male meiosis, pollen morphology, between B. divaricarpa and B. holboellii, and a low number of and flow-cytometry seed screens, we revealed an unexpected species-specific alleles suggests that the hybrid originated re- plethora of chromosome forms, pairing behavior, and hybrid cently (6). Multiple evolutionary origins of triploidy in Boechera composition in all apomictic lines. -
Oral Allergy Syndrome: a Confuence of Immunology and Phylogeny by Merle K
NATIONAL CENTER FOR CASE STUDY TEACHING IN SCIENCE NATIONAL CENTER FOR CASE STUDY TEACHING IN SCIENCE Oral Allergy Syndrome: A Confuence of Immunology and Phylogeny by Merle K. Heidemann, Mike S. Taylor, Amanda Storm, Cassie Dresser-Briggs, Alexa Warwick, and Peter J.T. White Objectives Upon completion of this case study, you should be able to: • Explain the symptoms of allergic reactions in terms of cell biology (immune system cells). • Describe the molecular features of cross reactivity. • Build phylogenetic trees using morphological data. • Build phylogenetic trees using molecular data and interpret two kinds of phylogenetic trees. Part I – Immunology Sam had a history of allergic reactions, including reactions to various plant pollens. Birch pollen elicited a particularly strong reaction, causing him annoying sneezing fts and a sore throat. As he grew to adulthood, he discovered that he was also variably allergic to common foods, including some raw fruits and vegetables, as well as most nuts. Sam was puzzled by his recent food allergies. Also puzzling was the variability in his reactions. He reacted strongly to some foods; others resulted in only a mild itchy throat. He wondered, What exactly causes allergic reactions? Sam was determined to fgure out how and why he reacted to birch pollen and later became allergic to other plant- based food. He also hoped this information might help him avoid other foods that might cause him allergies. First, Sam decided he needed to know something about the cellular bases of allergic reactions. He knew it had some- thing to do with the immune system. He did some basic research on the Internet and here’s what he found: Allergens are bits of protein from an innocuous foreign substance, such as pollen or food.