Chloroplast Genomes of Seven Coryloideae Species: Structures and Comparative Analysis

Total Page:16

File Type:pdf, Size:1020Kb

Chloroplast Genomes of Seven Coryloideae Species: Structures and Comparative Analysis Genome Chloroplast genomes of seven Coryloideae species: structures and comparative analysis Journal: Genome Manuscript ID gen-2019-0153.R1 Manuscript Type: Article Date Submitted by the 22-Feb-2020 Author: Complete List of Authors: Hu, Guanglong; Beijing Academy of Forestry and Pomology Sciences; Beijing Academy of Agricultural and Forestry Sciences, National Forestry and Grassland Administration, Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology Research Center, Key LaboratoryDraft of Biology and Genetic Improvement of Horticultural Crops (North China) Cheng, Lili; Beijing Academy of Forestry and Pomology Sciences; Beijing Academy of Agricultural and Forestry Sciences, National Forestry and Grassland Administration, Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology Research Center, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China) Huang, Wugang; Beijing Academy of Forestry and Pomology Sciences; Beijing Academy of Agricultural and Forestry Sciences, National Forestry and Grassland Administration, Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology Research Center, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China) Cao, Qingchang; Beijing Academy of Forestry and Pomology Sciences; Beijing Academy of Agricultural and Forestry Sciences, National Forestry and Grassland Administration, Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology Research Center, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China) Zhou, Lei; Hubei Academy of Agricultural Sciences, Food Crops Institute, Hubei Key Laboratory of Food Crop Germplasm and Genetic Improvement Jia, Wenshen; Beijing Academy of Agriculture and Forestry Science, Department of Beijing Research Center for Agricultural Standards and Testing Lan, Yanping; Beijing Academy of Forestry and Pomology Sciences; Beijing Academy of Agricultural and Forestry Sciences, National Forestry and Grassland Administration, Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology Research Center, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China) Corylus, Coryloideae, illumina sequencing, phylogenetic relationship, Keyword: Chloroplast genome (plastome) https://mc06.manuscriptcentral.com/genome-pubs Page 1 of 40 Genome Is the invited manuscript for consideration in a Special Not applicable (regular submission) Issue? : Draft https://mc06.manuscriptcentral.com/genome-pubs Genome Page 2 of 40 1 Title 2 Chloroplast genomes of seven Coryloideae ( Betulaceae ) species: structures and 3 comparative analysis 4 Authors and affiliations 5 ‘ 6 Guanglong Hua,b,†,*, Lili Chenga,b,†, Wugang Huanga,b, Qingchang Caoa,b, Lei Zhouc, 7 Wenshen Jiad, Yanping Lana,b,* 8 a Beijing Academy of Forestry and Pomology Sciences, Beijing 100093, China Draft 9 b Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North 10 China), Ministry of Agriculture and Rural Affairs/Chestnut Engineering Technology 11 Research Center, National Forestry and Grassland Administration, Beijing Academy of 12 Agricultural and Forestry Sciences, Beijing 100093, China 13 c Hubei Key Laboratory of Food Crop Germplasm and Genetic Improvement, Food 14 Crops Institute, Hubei Academy of Agricultural Sciences, Wuhan, Hubei 430064, 15 China 16 d Department of Beijing Research Center for Agricultural Standards and Testing, 17 Beijing Academy of Agriculture and Forestry Science, Beijing 100097, China 18 † The authors contributed equally to this work. 19 * Corresponding authors: Guanglong Hu (email: [email protected]) and Yanping Lan 20 ([email protected]). 1 https://mc06.manuscriptcentral.com/genome-pubs Page 3 of 40 Genome 21 Abstract 22 Coryloideae is a subfamily in the family Betulaceae consisting of four extant genera 23 Carpinus, Corylus, Ostrya , and Ostryopsis. We sequenced the plastomes of six 24 Corylus and one Ostryopsis species for comparative and phylogenetic analyses. The 25 plastomes are 159–160 kb long and possess the typical quadripartite cp architecture. 26 The plastomes show moderate divergence and conserved arrangement. We pointed five 27 mutational hotspots: trnG-atpA, trnF-ndhJ, accD-psaI, ndhF-ccsA, and ycf1, by 28 comparing the Coryloideae plastomes. We brought the most complete phylogenomic 29 tree for the family Betulaceae Draftusing 68 plastomes. Our cp genomic sequence 30 phylogenetic analyses placed Carpinus, Ostrya and Ostryopsis in a clade together and 31 left Corylus in a separate clade. Within the genus Corylus, these analyses indicate the 32 existence of five subclades reflecting the phylogeographical relationships among the 33 species. The data offer significant genetic information for the identification of 34 Coryloideae species, taxonomic and phylogenetic studies, and molecular breeding. 35 Key words 36 Corylus, Coryloideae, chloroplast genome, illumina sequencing, phylogenetic 37 relationship. 2 https://mc06.manuscriptcentral.com/genome-pubs Genome Page 4 of 40 38 Introduction 39 The Betulaceae Gray.(birch) family has six genera containing 120–150 species 40 (Abbe, 1974; Chen, 1994; Furlow, 1990). A majority of the species in the family are 41 primarily concentrated in the northern hemisphere. The six Betulaceae genera are 42 divided into two main tribes: Betuleae (Alnus Mill.and Betula L. ), and Coryleae 43 (Carpinus L., Corylus L., Ostrya Scop. , and Ostryopsis Decne.) ( Prantl and Engler, 44 1887; Winkler, 1904;Crane, 1989). Some authors suggest that the two tribes should be 45 elevated to the subfamilies Betuloideae and Coryloideae ( Rendle, 1925; Jury, 1978; 46 Furlow, 1990; Chen et al., 1999). DraftMoreover, the position of Ostryopsis in Coryleae is 47 controversial ( Kuprianova, 1963; Abbe, 1974; Furlow, 1990; Chen, 1994 ). Several 48 opinions concerning the genetic relationships among the genera of Coryleae have been 49 presented in the literature, using morphological characters, as well as rbcL gene and 50 ribosomal internal transcribed spacer (ITS) sequences (Abbe, 1974; Furlow, 1990; 51 Bousquet et al., 1992; Chen, 1994) 52 Ostryopsis davidiana Decne., one of two species in the genus Ostryopsis, is natively 53 distributed across vast northern areas of China (Raven, 1975; Li and Skvortsov, 1999; 54 Tian et al., 2009). The genus Corylus has 14 to 18 species concentrated in the northern 55 hemisphere’s temperature areas (Chen et al., 1999). Seven of those species grow in 56 China and comprise three tree species (C. chinensis Franch, C. fargesii C.K. Schneider, 57 and C. ferox Wall) and four shrub species (C. heterophylla Fisch, C. yunnanensis A. 58 Camus, C. mandshurica Maxim, and C. wangii Hu) (Liang and Zhang, 1988). However, 3 https://mc06.manuscriptcentral.com/genome-pubs Page 5 of 40 Genome 59 there is disagreement about whether C. yunnanensis and C. wangii should be 60 recognized as distinct species (Whitcher and Wen, 2001; Yoo and Wen, 2007). In 61 addition, most species of Corylus can hybridize with each other to achieve the cpDNA 62 introgression and transfer interspecificly (Erdogan and Mehlenbacher,2000b), therefor 63 the phylogeny and species definition of Corylus are still not completed. 64 The majority of plant plastomes typically possess a quadripartite architecture: two 65 inverted repeats (IRa and IRb), a small single copy region (SSC), and a large single 66 copy region (LSC). The plastome is usually circular DNA, of which 115–165 kb is 67 highly conserved. It has a conserved gene order and gene content ( Dong et al., 68 2013b;Wambugu et al., 2015; AsafDraft et al., 2016). Comparatively, the substitution rate 69 of a plant nuclear genome is higher than that of a cp genome (Duchene and Bromham, 70 2013; Smith, 2015). Furthermore, the angiosperm plastome has a stable structure, and 71 offer genetic markers sufficient for genome-wide evolutionary investigation at various 72 taxonomic levels ( Wu et al., 2010; Dong et al., 2012; Zhang et al., 2017;Givnish et 73 al., 2018;). Even though the plant plastome is evolutionarily conserved, specific 74 lineages and genes exhibit accelerated evolution rates ( Wu et al., 2010; Gaut et al., 75 2011; Dong et al., 2012, 2013b; Duchene and Bromham, 2013; Smith, 2015; Wambugu 76 et al., 2015;Asaf et al., 2016; Zhang et al., 2017). For instance, ycf1, matK, and rbcL 77 are all used, serving as DNA markers for barcoding plants ( Hollingsworth et al., 2011; 78 Dong et al., 2015). Due to such features, the plastome is assumed to serve as a good 4 https://mc06.manuscriptcentral.com/genome-pubs Genome Page 6 of 40 79 model for the investigation of lineage-specific molecular evolution (Sanitá Lima et al., 80 2016). 81 The plastomes of one Ostryopsis species and six Corylus species were sequenced in 82 this study via a next-generation sequencing platform. We gained valuable plastome 83 information including the length and content of highly variable regions, indels, 84 microsatellites, and single nucleotide polymorphisms (SNPs) in this subfamily by 85 comparing plastomes. Also, we assessed the phylogenetic relationships within the 86 Betulaceae genera and among the seven Coryloideae species. 87 Materials and methods Draft 88 Materials and DNA extraction 89 Fresh leaves of five Corylus species and O. davidiana were collected in China in 90 regions of natural distribution (Table 1). Fresh leaves of C. avellana were obtained from 91 the Germplasm Resource Nursery, Beijing Academy of Forestry and Pomology
Recommended publications
  • Evidence of Low Chloroplast Genetic Diversity in Two Carpinus Species
    Available online: www.notulaebotanicae.ro Print ISSN 0255-965X; Electronic 1842-4309 Not Bot Horti Agrobo, 2017, 45(1):316-322. DOI:10.15835/nbha45110799 Original Article Evidence of Low Chloroplast Genetic Diversity in Two Carpinus Species in the Northern Balkans Mihaela Cristina CĂRĂBUŞ 1, Alexandru Lucian CURTU 1, Dragoş POSTOLACHE 2, Elena CIOCÎRLAN 1, Neculae ŞOFLETEA 1* 1Transilvania University of Brasov, Department of Forest Sciences, 1 Şirul Beethoven, 500123, Braşov, Romania; [email protected] ; [email protected] ; [email protected] ; [email protected] (*corresponding author) 2National Research and Development Institute in Forestry “Marin Dracea”, 65 Horea Str., 400275 Cluj-Napoca, Romania; [email protected] Abstract Genetic diversity and differentiation in two Carpinus species ( C. betulus and C. orientalis ) occurring in Romania was investigated by using three chloroplast Simple Sequence Repeat markers (cpSSRs). A total of 96 and 32 individuals were sampled in eighteen C. betulus and six C. orientalis populations, respectively. A total of four chloroplast haplotypes were observed. Two haplotypes were specific for C. betulus and two for C. orientalis . Most of C. betulus populations were fixed for the predominant haplotype (H1), which was observed in 82% of the individuals. All C. orientalis populations were fixed for one haplotype or the other. Populations with haplotype (H3) are spread in southern Romania and the haplotype (H4) was observed at the northern limit of C. orientalis natural distribution range. Genetic differentiation among populations was moderate in C. betulus (GST = 0.422), compared to the high value observed in C. orientalis (GST = 1.000), which can be explained by the occurrence of a distinct haplotype in the peripheral population.
    [Show full text]
  • Global Survey of Ex Situ Betulaceae Collections Global Survey of Ex Situ Betulaceae Collections
    Global Survey of Ex situ Betulaceae Collections Global Survey of Ex situ Betulaceae Collections By Emily Beech, Kirsty Shaw and Meirion Jones June 2015 Recommended citation: Beech, E., Shaw, K., & Jones, M. 2015. Global Survey of Ex situ Betulaceae Collections. BGCI. Acknowledgements BGCI gratefully acknowledges the many botanic gardens around the world that have contributed data to this survey (a full list of contributing gardens is provided in Annex 2). BGCI would also like to acknowledge the assistance of the following organisations in the promotion of the survey and the collection of data, including the Royal Botanic Gardens Edinburgh, Yorkshire Arboretum, University of Liverpool Ness Botanic Gardens, and Stone Lane Gardens & Arboretum (U.K.), and the Morton Arboretum (U.S.A). We would also like to thank contributors to The Red List of Betulaceae, which was a precursor to this ex situ survey. BOTANIC GARDENS CONSERVATION INTERNATIONAL (BGCI) BGCI is a membership organization linking botanic gardens is over 100 countries in a shared commitment to biodiversity conservation, sustainable use and environmental education. BGCI aims to mobilize botanic gardens and work with partners to secure plant diversity for the well-being of people and the planet. BGCI provides the Secretariat for the IUCN/SSC Global Tree Specialist Group. www.bgci.org FAUNA & FLORA INTERNATIONAL (FFI) FFI, founded in 1903 and the world’s oldest international conservation organization, acts to conserve threatened species and ecosystems worldwide, choosing solutions that are sustainable, based on sound science and take account of human needs. www.fauna-flora.org GLOBAL TREES CAMPAIGN (GTC) GTC is undertaken through a partnership between BGCI and FFI, working with a wide range of other organisations around the world, to save the world’s most threated trees and the habitats which they grow through the provision of information, delivery of conservation action and support for sustainable use.
    [Show full text]
  • Number 3, Spring 1998 Director’S Letter
    Planning and planting for a better world Friends of the JC Raulston Arboretum Newsletter Number 3, Spring 1998 Director’s Letter Spring greetings from the JC Raulston Arboretum! This garden- ing season is in full swing, and the Arboretum is the place to be. Emergence is the word! Flowers and foliage are emerging every- where. We had a magnificent late winter and early spring. The Cornus mas ‘Spring Glow’ located in the paradise garden was exquisite this year. The bright yellow flowers are bright and persistent, and the Students from a Wake Tech Community College Photography Class find exfoliating bark and attractive habit plenty to photograph on a February day in the Arboretum. make it a winner. It’s no wonder that JC was so excited about this done soon. Make sure you check of themselves than is expected to seedling selection from the field out many of the special gardens in keep things moving forward. I, for nursery. We are looking to propa- the Arboretum. Our volunteer one, am thankful for each and every gate numerous plants this spring in curators are busy planting and one of them. hopes of getting it into the trade. preparing those gardens for The magnolias were looking another season. Many thanks to all Lastly, when you visit the garden I fantastic until we had three days in our volunteers who work so very would challenge you to find the a row of temperatures in the low hard in the garden. It shows! Euscaphis japonicus. We had a twenties. There was plenty of Another reminder — from April to beautiful seven-foot specimen tree damage to open flowers, but the October, on Sunday’s at 2:00 p.m.
    [Show full text]
  • Assessing the Effects of Vegetation Types on Carbon Storage Fifteen
    Forest Ecology and Management 258 (2009) 1437–1441 Contents lists available at ScienceDirect Forest Ecology and Management journal homepage: www.elsevier.com/locate/foreco Assessing the effects of vegetation types on carbon storage fifteen years after reforestation on a Chinese fir site Qinkui Wang a, Silong Wang a,b,*, Jianwei Zhang c a Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, PR China b Huitong Experimental Station of Forest Ecology, Chinese Academy of Sciences, Huitong 418307, PR China c USDA Forest Service, Pacific Southwest Research Station, 3644 Avtech Parkway, Redding, CA 96002, USA ARTICLE INFO ABSTRACT Article history: Forest ecosystems play a significant role in sequestering carbon (C) in biomass and soils. Plantations Received 13 April 2009 established in subtropical China since the 1980s, mainly of Chinese fir (Cunninghamia lanceolata (Lamb.) Received in revised form 9 June 2009 Hook) in monocultures, have proved to be major C sinks. However, information is lacking about whether Accepted 27 June 2009 mixing Chinese fir with broadleaved tree species will increase stand growth and C sequestration. We address this question by comparing a pure Chinese fir plantation and two mixed plantations established Keywords: in 1990 at Huitong Experimental Station of Forest Ecology, Hunan Province, China. The mixed Carbon storage plantations include Chinese fir and either Kalopanax septemlobus (Thunb.) Koidz or Alnus cremastogyne Mixed plantation Burk., planted at 4:1 ratios. We found that total C storage was 123, 131 and 142 Mg haÀ1 in the pure Broadleaved tree Coniferous plantation plantation, mixed plantation with K. septemlobus, and mixed plantation with A. cremastogyne, respectively.
    [Show full text]
  • A Critical Taxonomic Checklist of Carpinus and Ostrya (Coryloideae, Betulaceae)
    © European Journal of Taxonomy; download unter http://www.europeanjournaloftaxonomy.eu; www.zobodat.at European Journal of Taxonomy 375: 1–52 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.375 www.europeanjournaloftaxonomy.eu 2017 · Holstein N. & Weigend M. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph No taxon left behind? – a critical taxonomic checklist of Carpinus and Ostrya (Coryloideae, Betulaceae) Norbert HOLSTEIN 1,* & Maximilian WEIGEND 2 1,2 Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Nordrhein-Westfalen, Germany. * Corresponding author: [email protected] 2 Email: [email protected] Abstract. Hornbeams (Carpinus) and hop-hornbeams (Ostrya) are trees or large shrubs from the northern hemisphere. Currently, 43 species of Carpinus (58 taxa including subdivisions) and 8 species of Ostrya (9 taxa including sudivisions) are recognized. These are based on 175 (plus 16 Latin basionyms of cultivars) and 21 legitimate basionyms, respectively. We present an updated checklist with publication details and type information for all accepted names and the vast majority of synonyms of Carpinus and Ostrya, including the designation of 54 lectotypes and two neotypes. Cultivars are listed if validly described under the rules of the ICN. Furthermore, we consider Carpinus hwai Hu & W.C.Cheng to be a synonym of Carpinus fargesiana var. ovalifolia (H.J.P.Winkl.) Holstein & Weigend comb. nov. During the course of our work, we found 30 legitimate basionyms of non-cultivars that have been consistently overlooked since their original descriptions, when compared with the latest checklists and fl oristic treatments. As regional fl oras are highly important for taxonomic practice, we investigated the number of overlooked names and found that 78 basionyms were omitted at least once in the eight regional treatments surveyed.
    [Show full text]
  • (Carpinus Turczaninovii) Based on Nuclear Ribosomal ITS Sequence
    African Journal of Biotechnology Vol. 10(76), pp. 17435-17442, 30 November, 2011 Available online at http://www.academicjournals.org/AJB DOI: 10.5897/AJB11.1337 ISSN 1684–5315 © 2011 Academic Journals Full Length Research Paper Phylogeny of Korean Hornbeam ( Carpinus turczaninovii ) based on nuclear ribosomal ITS sequence Sun, Y. L. 1, Wang, D. 1, Lee, H. B.2, Park, W. G. 2, Kwon, O. W. 3 and Hong, S. K.1,4 * 1Department of Bio-Health Technology, Kangwon National University, Chuncheon, Kangwon-Do, 200-701, Korea. 2Department of Forest Resources, Kangwon National University, Chuncheon, Kangwon-Do, 200-701, Korea. 3Korea Forest Seed and Variety Center, Suanbo, Chungju, Chungcheongbuk-Do, 380-941, Korea. 4Division of Biomedical Technology, College of Biomedical Science, Chuncheon, Kangwon-Do, 200-701, Korea. Accepted 25 July, 2011 The genus Carpinus belonging to Coryloideae, Betulaceae, has significant economic and ornamental importance. This study was undertaken with the aim to understand the genetic diversity among eighteen isolates of Carpinus turczaninovii collected from different geographical regions of Korea, using ribosomal RNA (rRNA) internal transcribed spacer (ITS) sequences, to compare the infraspecific- phylogenetic relationships among C. turczaninovii in Korea, and some known Carpinus plants. The size variation of sequenced rRNA ITS regions was not seen, with 215, 162, 222 bp of ITS1 region, 5.8S rRNA gene, ITS2 region, respectively. However, some certain nucleotide variations resulted in genetic diversity. In the genus Carpinus , C. turczaninovii closely genetic with Castanopsis kawakamii , Carpinus orientalis , Carpinus monbeigiana , and Calyptranthes polynenra formed one monophyletic clade, while Carpinus betulus and Carpinus laxiflora, respectively formed one monophyletic clade.
    [Show full text]
  • A Critical Taxonomic Checklist of Carpinus and Ostrya (Coryloideae, Betulaceae)
    European Journal of Taxonomy 375: 1–52 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.375 www.europeanjournaloftaxonomy.eu 2017 · Holstein N. & Weigend M. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph No taxon left behind? – a critical taxonomic checklist of Carpinus and Ostrya (Coryloideae, Betulaceae) Norbert HOLSTEIN 1,* & Maximilian WEIGEND 2 1,2 Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Nordrhein-Westfalen, Germany. * Corresponding author: [email protected] 2 Email: [email protected] Abstract. Hornbeams (Carpinus) and hop-hornbeams (Ostrya) are trees or large shrubs from the northern hemisphere. Currently, 43 species of Carpinus (58 taxa including subdivisions) and 8 species of Ostrya (9 taxa including sudivisions) are recognized. These are based on 175 (plus 16 Latin basionyms of cultivars) and 21 legitimate basionyms, respectively. We present an updated checklist with publication details and type information for all accepted names and the vast majority of synonyms of Carpinus and Ostrya, including the designation of 54 lectotypes and two neotypes. Cultivars are listed if validly described under the rules of the ICN. Furthermore, we consider Carpinus hwai Hu & W.C.Cheng to be a synonym of Carpinus fargesiana var. ovalifolia (H.J.P.Winkl.) Holstein & Weigend comb. nov. During the course of our work, we found 30 legitimate basionyms of non-cultivars that have been consistently overlooked since their original descriptions, when compared with the latest checklists and fl oristic treatments. As regional fl oras are highly important for taxonomic practice, we investigated the number of overlooked names and found that 78 basionyms were omitted at least once in the eight regional treatments surveyed.
    [Show full text]
  • Integrating Molecular Tools and Conventional Approaches in the OSU Hazelnut Breeding Program
    Integrating Molecular Tools and Conventional Approaches in the OSU Hazelnut Breeding Program Shawn A. Mehlenbacher Dept. of Horticulture Oregon State University Workshop on the Genetics of Host-Parasite Interactions in Forestry Eugene, OR 31 July – 5 August 2011 Integrating Molecular Tools and Conventional Approaches in the OSU Hazelnut Breeding Program • Hazelnut, a model for the Betulaceae • Breeding program - the driving force • Eastern filbert blight resistance • DNA markers, marker-assisted selection, mapping • Microsatellite markers and uses • Map-based cloning (‘Gasaway’ EFB resistance gene) • Sequencing the hazelnut genome (and transcriptome) • HRM for marker-assisted selection • Quantitative EFB resistance Taxonomy of Hazelnut (Corylus) Angiosperms, Eudicots, Core Eudicots, Rosids Rosids: Order Fagales: from tolweb.org Family Betulaceae Betuloideae Betula = birch (35-50 species) Alnus = alder (35 species) Coryloideae Corylus = hazelnut, filbert (11-15 species) Ostrya = hophornbeam (10 species) Ostryopsis = hornbeam (2 species) There are 11 commonly recognized Corylus species, all native to the northern hemisphere. All species produce edible kernels, but only the European hazelnut is commercially important. Corylus species Leafy-husked shrubs C. avellana = European hazel Grown commercially C. americana = American hazel C. heterophylla = Siberian hazel Bristle-husked shrubs native to C. cornuta = beaked hazel North America C. californica = California hazel C. sieboldiana = Manchurian hazel Tree hazels C. colurna = Turkish tree
    [Show full text]
  • 100 Years of Change in the Flora of the Carolinas
    ASTERACEAE 224 Zinnia Linnaeus 1759 (Zinnia) A genus of about 17 species, herbs, of sw. North America south to South America. References: Smith in FNA (2006c); Cronquist (1980)=SE. 1 Achenes wingless; receptacular bracts (chaff) toothed or erose on the lip..............................................................Z. peruviana 1 Achenes winged; receptacular bracts (chaff) with a differentiated fimbriate lip........................................................Z. violacea * Zinnia peruviana (Linnaeus) Linnaeus, Zinnia. Cp (GA, NC, SC): disturbed areas; rare (commonly cultivated), introduced from the New World tropics. May-November. [= FNA, K, SE; ? Z. pauciflora Linnaeus – S] * Zinnia violacea Cavanilles, Garden Zinnia. Cp (GA, NC, SC): disturbed areas; rare (commonly cultivated), introduced from the New World tropics. May-November. [= FNA, K; ? Z. elegans Jacquin – S, SE] BALSAMINACEAE A. Richard 1822 (Touch-me-not Family) A family of 2 genera and 850-1000 species, primarily of the Old World tropics. References: Fischer in Kubitzki (2004). Impatiens Linnaeus (Jewelweed, Touch-me-not, Snapweed, Balsam) A genus of 850-1000 species, herbs and subshrubs, primarily tropical and north temperate Old World. References: Fischer in Kubitzki (2004). 1 Corolla purple, pink, or white; plants 3-6 (-8) dm tall; stems puberulent or glabrous; [cultivated alien, rarely escaped]. 2 Sepal spur strongly recurved; stems puberulent..............................................................................................I. balsamina 2 Sepal spur slightly
    [Show full text]
  • Cophorticultura 1(2019)
    Scientific Papers. Series B, Horticulture. Vol. LXIII, No. 1, 2019 Print ISSN 2285-5653, CD-ROM ISSN 2285-5661, Online ISSN 2286-1580, ISSN-L 2285-5653 HOW MANY ALDER SPECIES (ALNUS SP.) EXIST? A STATISTIC BASED ON HERBARIUM VOUCHERS Lucian DINCĂ1, Adrian PETICILĂ2 1“Marin Drăcea” National Institute for Research and Development in Forestry, 13 Closca St., Brasov, Romania 2University of Agronomic Sciences and Veterinary Medicine of Bucharest, Faculty of Horticulture, 59 Marasti Blvd., District 1, Bucharest, Romania Corresponding author email: [email protected] Abstract In the speciality literature, the number of Alnus species varies between 30 and 35. However, by analysing the species present in different herbarium (Al. Beldie Herbarium from Romania, WU Herbarium from Wien and Harvard University Herbaria from U.S.A.), this number increases to 42. The most numerous Alder species present in these herbariums are Alnus incana and Alnus viridis (spread out on a vast natural range, namely Eurasia and North America), followed by Alnus serrulata (which can be found in North America). As such, the Alnus Genus is well represented in Asia (especially in China and Japan), as well as in North America or Europe. The analysis of vouchers present in different herbariums has significant contributions regarding the number of species from a certain genus, their spreading, as well as their particular characteristics. However, in order to obtain satisfactory results, a large number of herbariums is required, followed by an appropriate geographic distribution. In this regard, the BUCF Romanian herbarium is a good case study. Key words: Alnus, herbarium, species, alder, voucher. INTRODUCTION The Alnus species can be recognized by their simple, deciduous and dented leaves.
    [Show full text]
  • Patterns in the Assembly of Temperate Forests Around the Northern Hemisphere
    Published online 7 October 2004 Patterns in the assembly of temperate forests around the Northern Hemisphere Michael J. Donoghueà and Stephen A. Smith Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520, USA Recent studies of Northern Hemisphere biogeography have highlighted potentially significant differences between disjunction patterns in plants versus animals. To assess such differences, we compiled a larger sam- ple of relevant plant phylogenies from which disjunction patterns, ancestral areas and directions of move- ment could be inferred. We considered 66 plant clades with species variously endemic today to eastern Asia (EA), Europe (including southwestern Asia), eastern North America (ENA), and/or western North America (WNA). Within these clades we focused on 100 disjunctions among these major areas, for 33 of which absol- ute divergence times have also been inferred. Our analyses uphold the view that disjunctions between EA and ENA are exceptionally common in plants, apparently more so than in animals. Compared with animals, we find few disjunctions between EA and WNA, consistent with increased extinction in WNA or failure of some groups to colonize that region. Taken at face value, our data also support the view that many temperate forest plant groups originated and diversified within EA, followed by movement out of Asia at different times, but mostly during the last 30 Myr. This favours Beringia over a North Atlantic land bridge as the primary path between the Old World and the New World. Additional studies are needed, especially to evalu- ate the impacts of differential extinction on these patterns, to more confidently establish divergence times, and to assess the statistical significance of these findings.
    [Show full text]
  • Supplementary Material
    Xiang et al., Page S1 Supporting Information Fig. S1. Examples of the diversity of diaspore shapes in Fagales. Fig. S2. Cladogram of Fagales obtained from the 5-marker data set. Fig. S3. Chronogram of Fagales obtained from analysis of the 5-marker data set in BEAST. Fig. S4. Time scale of major fagalean divergence events during the past 105 Ma. Fig. S5. Confidence intervals of expected clade diversity (log scale) according to age of stem group. Fig. S6. Evolution of diaspores types in Fagales with BiSSE model. Fig. S7. Evolution of diaspores types in Fagales with Mk1 model. Fig. S8. Evolution of dispersal modes in Fagales with MuSSE model. Fig. S9. Evolution of dispersal modes in Fagales with Mk1 model. Fig. S10. Reconstruction of pollination syndromes in Fagales with BiSSE model. Fig. S11. Reconstruction of pollination syndromes in Fagales with Mk1 model. Fig. S12. Reconstruction of habitat shifts in Fagales with MuSSE model. Fig. S13. Reconstruction of habitat shifts in Fagales with Mk1 model. Fig. S14. Stratigraphy of fossil fagalean genera. Table S1 Genera of Fagales indicating the number of recognized and sampled species, nut sizes, habits, pollination modes, and geographic distributions. Table S2 List of taxa included in this study, sources of plant material, and GenBank accession numbers. Table S3 Primers used for amplification and sequencing in this study. Table S4 Fossil age constraints utilized in this study of Fagales diversification. Table S5 Fossil fruits reviewed in this study. Xiang et al., Page S2 Table S6 Statistics from the analyses of the various data sets. Table S7 Estimated ages for all families and genera of Fagales using BEAST.
    [Show full text]