Epicuticular Flavonoids of Some Scrophulariaceae
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Think Outside the Box Page 1
LNewsletteret’s of the San DiegoT Horticulturalalk Society Pl ants! February 2016, Number 257 Think Outside the Box PAGE 1 Our Spring Garden Tour – pages 3 & 8 Auxins – page 5 Early Spring Bloomers – page 6 El Niño Garden Realities – page 9 On the Cover: Tropical look for the garden SPECIAL EVENT: Chinese Garden Bus Trip Huntington Botanical Gardens on Wednesday, April 20 Join SDHS members on a docent-led tour of the stunning Chinese Garden, among the largest Chinese-style gardens outside China. Designed to promote the rich traditions of Chinese culture, the garden is truly a cross-cultural effort. After the tour we’ll have about four hours to see other areas of the Botanical Gardens, including the new California Garden. The bus leaves San Diego at 7am and returns around 7:30pm. All fees & tip included; lunch at the Gardens is on your own. Members-$89, Guests-$99 Space is limited - register ASAP Details & registration at: sdhort.org ▼SDHS SPONSOR GREEN THUMB SUPER GARDEN CENTERS 1019 W. San Marcos Blvd. • 760-744-3822 (Off the 78 Frwy. near Via Vera Cruz) • CALIFORNIA NURSERY PROFESSIONALS ON STAFF • HOME OF THE NURSERY EXPERTS • GROWER DIRECT www.supergarden.com Now on Facebook WITH THIS VALUABLE Coupon $10 00 OFF Any Purchase of $6000 or More! • Must present printed coupon to cashier at time of purchase • Not valid with any sale items or with other coupons or offers • Offer does not include Sod, Gift Certifi cates, or Department 56 • Not valid with previous purchases • Limit 1 coupon per household • Coupon expires 2/29/2016 at 6 p.m. -
Lamiales – Synoptical Classification Vers
Lamiales – Synoptical classification vers. 2.6.2 (in prog.) Updated: 12 April, 2016 A Synoptical Classification of the Lamiales Version 2.6.2 (This is a working document) Compiled by Richard Olmstead With the help of: D. Albach, P. Beardsley, D. Bedigian, B. Bremer, P. Cantino, J. Chau, J. L. Clark, B. Drew, P. Garnock- Jones, S. Grose (Heydler), R. Harley, H.-D. Ihlenfeldt, B. Li, L. Lohmann, S. Mathews, L. McDade, K. Müller, E. Norman, N. O’Leary, B. Oxelman, J. Reveal, R. Scotland, J. Smith, D. Tank, E. Tripp, S. Wagstaff, E. Wallander, A. Weber, A. Wolfe, A. Wortley, N. Young, M. Zjhra, and many others [estimated 25 families, 1041 genera, and ca. 21,878 species in Lamiales] The goal of this project is to produce a working infraordinal classification of the Lamiales to genus with information on distribution and species richness. All recognized taxa will be clades; adherence to Linnaean ranks is optional. Synonymy is very incomplete (comprehensive synonymy is not a goal of the project, but could be incorporated). Although I anticipate producing a publishable version of this classification at a future date, my near- term goal is to produce a web-accessible version, which will be available to the public and which will be updated regularly through input from systematists familiar with taxa within the Lamiales. For further information on the project and to provide information for future versions, please contact R. Olmstead via email at [email protected], or by regular mail at: Department of Biology, Box 355325, University of Washington, Seattle WA 98195, USA. -
A Phylogenetic Study of the Tribe Antirrhineae: Genome Duplications and Long-Distance Dispersals from the Old World to the New World 1
RESEARCH ARTICLE AMERICAN JOURNAL OF BOTANY A phylogenetic study of the tribe Antirrhineae: Genome duplications and long-distance dispersals from the Old World to the New World 1 Ezgi Ogutcen2 and Jana C. Vamosi PREMISE OF THE STUDY: Antirrhineae is a large tribe within Plantaginaceae. Mostly concentrated in the Mediterranean Basin, the tribe members are present both in the Old World and the New World. Current Antirrhineae phylogenies have diff erent views on taxonomic relationships, and they lack homogeneity in terms of geographic distribution and ploidy levels. This study aims to investigate the changes in the chromosome numbers along with dispersal routes as defi nitive characters identifying clades. METHODS: With the use of multiple DNA regions and taxon sampling enriched with de novo sequences, we provide an extensive phylogeny for Antir- rhineae. The reconstructed phylogeny was then used to investigate changes in ploidy levels and dispersal patterns in the tribe using ChromEvol and RASP, respectively. KEY RESULTS: Antirrhineae is a monophyletic group with six highly supported clades. ChromEvol analysis suggests the ancestral haploid chromosome number for the tribe is six, and that the tribe has experienced several duplications and gain events. The Mediterranean Basin was estimated to be the origin for the tribe with four long-distance dispersals from the Old World to the New World, three of which were associated with genome duplications. CONCLUSIONS: On an updated Antirrhineae phylogeny, we showed that the three out of four dispersals from the Old World to the New World were coupled with changes in ploidy levels. The observed patterns suggest that increases in ploidy levels may facilitate dispersing into new environments. -
Rare Plant Register
1 BSBI RARE PLANT REGISTER Berkshire & South Oxfordshire V.C. 22 MICHAEL J. CRAWLEY FRS UPDATED APRIL 2005 2 Symbols and conventions The Latin binomial (from Stace, 1997) appears on the left of the first line in bold, followed by the authority in Roman font and the English Name in italics. Names on subsequent lines in Roman font are synonyms (including names that appear in Druce’s (1897) or Bowen’s (1964) Flora of Berkshire that are different from the name of the same species in Stace). At the right hand side of the first line is a set of symbols showing - status (if non-native) - growth form - flowering time - trend in abundance (if any) The status is one of three categories: if the plant arrived in Britain after the last ice age without the direct help of humans it is defined as a native, and there is no symbol in this position. If the archaeological or documentary evidence indicates that a plant was brought to Berkshire intentionally of unintentionally by people, then that species is an alien. The alien species are in two categories ● neophytes ○ archaeophytes Neophytes are aliens that were introduced by people in recent times (post-1500 by convention) and for which we typically have precise dates for their first British and first Berkshire records. Neophytes may be naturalized (forming self-replacing populations) or casual (relying on repeated introduction). Archaeophytes are naturalized aliens that were carried about by people in pre-historic times, either intentionally for their utility, or unintentionally as contaminants of crop seeds. Archaeophytes were typically classified as natives in older floras. -
Pollinator Adaptation and the Evolution of Floral Nectar Sugar
doi: 10.1111/jeb.12991 Pollinator adaptation and the evolution of floral nectar sugar composition S. ABRAHAMCZYK*, M. KESSLER†,D.HANLEY‡,D.N.KARGER†,M.P.J.MULLER€ †, A. C. KNAUER†,F.KELLER§, M. SCHWERDTFEGER¶ &A.M.HUMPHREYS**†† *Nees Institute for Plant Biodiversity, University of Bonn, Bonn, Germany †Institute of Systematic and Evolutionary Botany, University of Zurich, Zurich, Switzerland ‡Department of Biology, Long Island University - Post, Brookville, NY, USA §Institute of Plant Science, University of Zurich, Zurich, Switzerland ¶Albrecht-v.-Haller Institute of Plant Science, University of Goettingen, Goettingen, Germany **Department of Life Sciences, Imperial College London, Berkshire, UK ††Department of Ecology, Environment and Plant Sciences, University of Stockholm, Stockholm, Sweden Keywords: Abstract asterids; A long-standing debate concerns whether nectar sugar composition evolves fructose; as an adaptation to pollinator dietary requirements or whether it is ‘phylo- glucose; genetically constrained’. Here, we use a modelling approach to evaluate the phylogenetic conservatism; hypothesis that nectar sucrose proportion (NSP) is an adaptation to pollina- phylogenetic constraint; tors. We analyse ~ 2100 species of asterids, spanning several plant families pollination syndrome; and pollinator groups (PGs), and show that the hypothesis of adaptation sucrose. cannot be rejected: NSP evolves towards two optimal values, high NSP for specialist-pollinated and low NSP for generalist-pollinated plants. However, the inferred adaptive process is weak, suggesting that adaptation to PG only provides a partial explanation for how nectar evolves. Additional factors are therefore needed to fully explain nectar evolution, and we suggest that future studies might incorporate floral shape and size and the abiotic envi- ronment into the analytical framework. -
Leaf Epidermis: the Ambiguous Symplastic Domain
ORIGINAL RESEARCH published: 29 July 2021 doi: 10.3389/fpls.2021.695415 Leaf Epidermis: The Ambiguous Symplastic Domain Olga V. Voitsekhovskaja 1,2*, Anna N. Melnikova 1,3, Kirill N. Demchenko 1, Alexandra N. Ivanova 1,3, Valeria A. Dmitrieva 1, Anastasiia I. Maksimova 1, Gertrud Lohaus 2,4, A. Deri Tomos 5, Elena V. Tyutereva 1 and Olga A. Koroleva 5 1 Komarov Botanical Institute, Russian Academy of Sciences, Saint Petersburg, Russia, 2 Department of Plant Biochemistry, Albrecht von Haller Institute for Plant Sciences, Göttingen, Germany, 3 Saint Petersburg State University, Saint Petersburg, Russia, 4 Molecular Plant Research/Plant Biochemistry, School of Mathematics and Natural Sciences, University of Wuppertal, Wuppertal, Germany, 5 School of Biological Sciences, Bangor University, Bangor, United Kingdom The ability to develop secondary (post-cytokinetic) plasmodesmata (PD) is an important Edited by: evolutionary advantage that helps in creating symplastic domains within the plant body. Jung-Youn Lee, University of Delaware, United States Developmental regulation of secondary PD formation is not completely understood. In Reviewed by: flowering plants, secondary PD occur exclusively between cells from different lineages, Chul Min Kim, e.g., at the L1/L2 interface within shoot apices, or between leaf epidermis (L1-derivative), Wonkwang University, South Korea John Larkin, and mesophyll (L2-derivative). However, the highest numbers of secondary PD occur Louisiana State University, in the minor veins of leaf between bundle sheath cells and phloem companion cells United States in a group of plant species designated “symplastic” phloem loaders, as opposed *Correspondence: to “apoplastic” loaders. This poses a question of whether secondary PD formation Olga V. -
WRA Species Report
Family: Plantaginaceae Taxon: Lophospermum erubescens Synonym: Asarina erubescens (D. Don) Pennell Common Name: larger roving sailor Maurandya erubescens (D. Don) A. Gray creeping gloxinia Maurandya scandens var. erubescens (D. Don Mexican twist Questionaire : current 20090513 Assessor: Chuck Chimera Designation: H(HPWRA) Status: Assessor Approved Data Entry Person: Chuck Chimera WRA Score 10 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? y=1, n=-1 103 Does the species have weedy races? y=1, n=-1 201 Species suited to tropical or subtropical climate(s) - If island is primarily wet habitat, then (0-low; 1-intermediate; 2- High substitute "wet tropical" for "tropical or subtropical" high) (See Appendix 2) 202 Quality of climate match data (0-low; 1-intermediate; 2- High high) (See Appendix 2) 203 Broad climate suitability (environmental versatility) y=1, n=0 y 204 Native or naturalized in regions with tropical or subtropical climates y=1, n=0 y 205 Does the species have a history of repeated introductions outside its natural range? y=-2, ?=-1, n=0 y 301 Naturalized beyond native range y = 1*multiplier (see y Appendix 2), n= question 205 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see n Appendix 2) 304 Environmental weed n=0, y = 2*multiplier (see y Appendix 2) 305 Congeneric weed n=0, y = 1*multiplier (see n Appendix 2) 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic -
Lophospermum Erubescens D.Don Family: Plantaginaceae Don, D
Australian Tropical Rainforest Plants - Online edition Lophospermum erubescens D.Don Family: Plantaginaceae Don, D. (1832) The British Flower Garden Ser. 2, 1: 68. Type: "The seeds of the above interesting plant were obtained from specimens collected in thickets, near Jalapa, in September, 1829, by Messrs. Deppe and Schiede, two German Botanists, who have been for some time in Mexico." Common name: Climbing Lophospermum; Maurandia; Lophospermum, Climbing; Creeping Gloxinia; Gloxinia, Creeping; Snapdragon Vine; Vine, Snapdragon; Snapdragon, Climbing; Climbing Snapdragon Stem A slender vine not exceeding a stem diameter of 2 cm. Leaves Leaf blades ovate-cordate, very soft, about 6-8 x 6-8 cm, margin with 1 or 2 lobes on each side towards the base and about 18-20 rounded teeth on each side. Petiole about 4.5-6 cm long, often modified to form coiled tendrils. Upper and lower leaf blades surfaces densely clothed in pale simple Flowers. © CSIRO hairs. Lateral veins poorly developed. Flowers Peduncles about 20-25 mm long. Sepals ovate, about 25 x 15 mm, densely hairy on both surfaces, folded near the base. Corolla tube curved, about 60 mm long, throat white. Corolla lobes about 12 x 15-16 mm, apices rounded. Stamens attached near the base of the corolla tube. Staminal filaments about 35-45 mm long, 2 long and 2 shorter, clothed in glandular hairs on the upper half with a large glandular appendage near the apex. Ovary hairy, about 4 mm long. Style hairy towards the base. Ovules numerous. Fruit. © CSIRO Fruit Fruits +/- bilobed, about 16 x 23 x 15 mm, calyx lobes rather large, persistent at the base, stylar remnants often persistent at the apex. -
Pollinator Attractors: Petaloidy and Petal Epidermal Cell Shape in Close Relatives of Snapdragon
Pollinator attractors: petaloidy and petal epidermal cell shape in close relatives of snapdragon By Copyright 2011 Jacob Brian Landis Submitted to the graduate degree program in Ecology and Evolutionary Biology and the Graduate Faculty of the University of Kansas in partial fulfillment of the requirements for the degree of Master of Arts. ________________________________ Chairperson Dr. Lena Hileman ________________________________ Dr. Mark Mort ________________________________ Dr. Paulyn Cartwright Date Defended: April 13, 2011 ii The Thesis Committee for Jacob B Landis certifies that this is the approved version of the following thesis: Pollinator attractors: petaloidy and petal epidermal cell shape in close relatives of snapdragon ________________________________ Chairperson Dr. Lena Hileman Date approved: 30 June 2011 1 ABSTRACT The diversity of angiosperms in floral form and development has been an area of interest for biologists. A multitude of studies investigating the evolution of flowering plants have attempted to determine why angiosperms are so diverse. One possible major contributor to flower form diversity is pollinator pressure. The interactions between flowers and their pollinators have important ecological and evolutionary consequences, with co-evolution often occuring. Many studies have looked at suites of floral traits that affect pollinator visitation, which have been coined pollination syndromes (Fenster et al., 2004). These traits include but are not limited to, flower color, flower orientation, landing platforms, and nectar guides. With the increase in genetic tools, and the utilization of model species such as Antirrhinum majus(Plantaginaceae) and Arabidopsis thaliana (Brassicaeae), many studies are looking at the geneitc architecture of floral traits. Studies have determined the genetic blueprint for floral oragn identity, as well as in traits asociated with pollination syndromes including flower color and symmetry. -
Pack Trials 2004 — Part I
june 04 9/10/04 7:26 AM Page 20 vegetative matters companion coverage Pick of the Pack Trials, Part I . .page 30 A Pack Trial Adventure . .page 48 Pack Trials 2004 — Part I So many good plants, so little time. By Rick Schoellhorn University of Florida he 2004 Pack Trials was a great experi- ence this year. A lot of fantastic plant material, some killerT new plant materials and some companies that really hit their stride and made some big advances in trials and displays. There was a bit more emphasis put back on comparison trialing which is always good to see. I wasn’t around for the early days of Pack Trials when the main thrust was comparative trialing, but it is great to see some of that mixed in with displays of current releases in their prime. It was not an easy year to put on a good display, as temperatures in California were soaring and plung- ing all spring, making it difficult to time crops for the trials. We also went through trials on the last days of the event so some of the truly early cool season crops were a little past peak. It also seemed that the number of new releases were, in general, a little more con- Clockwise from top: ‘Raspberry Smoothie’ thunbergia (Ecke); rhodochiton (Benary); ‘Wine Red’ lophospermum (Suntory). servative this year, and given the recent political and economical cli- SOME STANDOUTS we are focusing on in our trials this All America Selection and is noted mate, I guess that is to be expected. -
Worldwide Biogeography of Snapdragons and Relatives
SUPPORTING INFORMATION Out of the Mediterranean Region: worldwide biogeography of snapdragons and relatives (tribe Antirrhineae, Plantaginaceae) Juan Manuel Gorospe, David Monjas, Mario Fernández-Mazuecos Appendix S1. Supplementary text. Table S1. GenBank accession numbers for previously published and newly generated DNA sequences of Antirrhineae and the outgroup used in the present study. Table S2. Vouchers specimens for newly-sequenced taxa of Antirrhineae. Table S3. Distribution ranges of taxa used in biogeographic analyses. Table S4. Comparison of biogeographic models in BioGeoBEARS. Fig. S1. Dispersal probability matrices for each time slice and maps representing a schematic configuration of landmasses. Fig. S2. Bayesian phylogenetic tree of Antirrhineae based on analysis of ITS, ndhF and rpl32-trnL sequences in MrBayes. Fig. S3. Maximum clade credibility tree from phylogenetic analysis in BEAST. Fig. S4. S-DIVA ancestral range estimation in RASP. Fig. S5. Ancestral range estimation under the DEC model in BioGeoBEARS (with dispersal scalars). Appendix S1. Supplementary text. MATERIALS AND METHODS DNA sequencing DNA regions ITS, ndhF and rpl32-trnL were selected according to previous studies (Fernández-Mazuecos, Blanco-Pastor, Gómez, & Vargas, 2013; Fernández-Mazuecos et al., 2019; Fernández-Mazuecos, Blanco-Pastor, & Vargas, 2013; Fernández-Mazuecos & Vargas, 2011; Ghebrehiwet, Bremer, & Thulin, 2000; Vargas, Rosselló, Oyama, & Güemes, 2004). DNA extractions were obtained using the DNeasy Plant Mini Kit (Qiagen, CA, USA). PCR amplification followed the methods of Fernández-Mazuecos, Blanco-Pastor, and Vargas (2013) for ITS and Fernández-Mazuecos and Vargas (2011) for rpl32-trnL. Amplified products were submitted to Macrogen Inc. (Macrogen Europe, Madrid, Spain) for Sanger sequencing using primers P1A and P4 for the ITS region (Sang, Crawford, & Stuessy, 1995; White, Bruns, Lee, & Taylor, 1990) and trnL(UAG) and rpl32F for the rpl32-trnL region (Shaw, Lickey, Schilling, & Small, 2007). -
Lophospermum Erubescens Click on Images to Enlarge
Species information Abo ut Reso urces Hom e A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Lophospermum erubescens Click on images to enlarge Family Plantaginaceae Scientific Name Lophospermum erubescens D.Don Don, D. (1832) The British Flower Garden Ser. 2, 1: 68. Type: "The seeds of the above interesting plant were obtained from specimens collected in thickets, near Jalapa, in September, 1829, by Messrs. Deppe and Schiede, two German Botanists, who have been for some time in Mexico." Flowers. Copyright CSIRO Common name Climbing Lophospermum; Maurandia; Lophospermum, Climbing; Creeping Gloxinia; Gloxinia, Creeping; Snapdragon Vine; Vine, Snapdragon; Snapdragon, Climbing; Climbing Snapdragon Weed * Stem Fruit. Copyright CSIRO A slender vine not exceeding a stem diameter of 2 cm. Leaves Leaf blades ovate-cordate, very soft, about 6-8 x 6-8 cm, margin with 1 or 2 lobes on each side towards the base and about 18-20 rounded teeth on each side. Petiole about 4.5-6 cm long, often modified to form coiled tendrils. Upper and lower leaf blades surfaces densely clothed in pale simple hairs. Lateral veins poorly developed. Flowers Scale bar 10mm. Copyright CSIRO Peduncles about 20-25 mm long. Sepals ovate, about 25 x 15 mm, densely hairy on both surfaces, folded near the base. Corolla tube curved, about 60 mm long, throat white. Corolla lobes about 12 x 15-16 mm, apices rounded. Stamens attached near the base of the corolla tube. Staminal filaments about 35-45 mm long, 2 long and 2 shorter, clothed in glandular hairs on the upper half with a large glandular appendage near the apex.