Thlaspi Arvense L. Common Name: Field Pennycress Assessors: Timm Nawrocki Lindsey A
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(Cruciferae) – Mustard Family
BRASSICACEAE (CRUCIFERAE) – MUSTARD FAMILY Plant: herbs mostly, annual to perennial, sometimes shrubs; sap sometimes peppery Stem: Root: Leaves: mostly simple but sometimes pinnately divided; alternate, rarely opposite or whorled; no stipules Flowers: mostly perfect, mostly regular (actinomorphic); 4 sepals, 4 petals often forming a cross; 6 stamens with usually 2 outer ones shorter than the inner 4; ovary superior, mostly 2 fused carpels, 1 to many ovules, 1 pistil Fruit: seed pods, often used in classification, many are slender and long (Silique), some broad (Silicle) – see morphology slide Other: a large family, many garden plants such as turnip, radish, and cabbage, also some spices; often termed the Cruciferae family; Dicotyledons Group Genera: 350+ genera; 40+ locally WARNING – family descriptions are only a layman’s guide and should not be used as definitive Flower Morphology in the Brassicaceae (Mustard Family) - flower with 4 sepals, 4 petals (often like a cross, sometimes split or lobed), commonly small, often white or yellow, distinctive fruiting structures often important for ID 2 types of fruiting pods: in addition, fruits may be circular, flattened or angled in cross-section Silicle - (usually <2.5x long as wide), 2-valved with septum (replum) Silique - (usually >2.5x long as wide), 2- valved with septum (replum) Flowers, Many Genera BRASSICACEAE (CRUCIFERAE) – MUSTARD FAMILY Sanddune [Western] Wallflower; Erysimum capitatum (Douglas ex Hook.) Greene var. capitatum Wormseed Wallflower [Mustard]; Erysimum cheiranthoides L. (Introduced) Spreading Wallflower [Treacle Mustard]; Erysimum repandum L. (Introduced) Dame’s Rocket [Dame’s Violet]; Hesperis matronalis L. (Introduced) Purple [Violet] Rocket; Iodanthus pinnatifidus (Michx.) Steud. Michaux's Gladecress; Leavenworthia uniflora (Michx.) Britton [Cow; Field] Cress [Peppergrass]; Lepidium campestre L.) Ait. -
Seed Ecology Iii
SEED ECOLOGY III The Third International Society for Seed Science Meeting on Seeds and the Environment “Seeds and Change” Conference Proceedings June 20 to June 24, 2010 Salt Lake City, Utah, USA Editors: R. Pendleton, S. Meyer, B. Schultz Proceedings of the Seed Ecology III Conference Preface Extended abstracts included in this proceedings will be made available online. Enquiries and requests for hardcopies of this volume should be sent to: Dr. Rosemary Pendleton USFS Rocky Mountain Research Station Albuquerque Forestry Sciences Laboratory 333 Broadway SE Suite 115 Albuquerque, New Mexico, USA 87102-3497 The extended abstracts in this proceedings were edited for clarity. Seed Ecology III logo designed by Bitsy Schultz. i June 2010, Salt Lake City, Utah Proceedings of the Seed Ecology III Conference Table of Contents Germination Ecology of Dry Sandy Grassland Species along a pH-Gradient Simulated by Different Aluminium Concentrations.....................................................................................................................1 M Abedi, M Bartelheimer, Ralph Krall and Peter Poschlod Induction and Release of Secondary Dormancy under Field Conditions in Bromus tectorum.......................2 PS Allen, SE Meyer, and K Foote Seedling Production for Purposes of Biodiversity Restoration in the Brazilian Cerrado Region Can Be Greatly Enhanced by Seed Pretreatments Derived from Seed Technology......................................................4 S Anese, GCM Soares, ACB Matos, DAB Pinto, EAA da Silva, and HWM Hilhorst -
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 -
Example Pennycress (Thlaspi Arvense L.)
Plant Science 227 (2014) 122–132 Contents lists available at ScienceDirect Plant Science j ournal homepage: www.elsevier.com/locate/plantsci Review New approaches to facilitate rapid domestication of a wild plant to an oilseed crop: Example pennycress (Thlaspi arvense L.) a,∗ b c John C. Sedbrook , Winthrop B. Phippen , M. David Marks a School of Biological Sciences, Illinois State University, Campus Box 4120, Normal, IL 61790 USA b School of Agriculture, Western Illinois University, 1 University Circle, Macomb, IL 61455, USA c Department of Plant Biology, University of Minnesota, 1445 Gortner Avenue, 250 Biological Sciences Center, Saint Paul, MN 55108, USA a r t i c l e i n f o a b s t r a c t Article history: Oilseed crops are sources of oils and seed meal having a multitude of uses. While the domestication of Received 20 May 2014 soybean and rapeseed took extended periods of time, new genome-based techniques have ushered in Received in revised form 23 July 2014 an era where crop domestication can occur rapidly. One attractive target for rapid domestication is the Accepted 25 July 2014 winter annual plant Field Pennycress (Thlaspi arvense L.; pennycress; Brassicaceae). Pennycress grows Available online 4 August 2014 widespread throughout temperate regions of the world and could serve as a winter oilseed-producing cover crop. If grown throughout the USA Midwest Corn Belt, for example, pennycress could produce as Keywords: much as 840 L/ha oils and 1470 kg/ha press-cake annually on 16 million hectares of farmland currently Oilseed left fallow during the fall through spring months. -
Biogeography and Diversification of Brassicales
Molecular Phylogenetics and Evolution 99 (2016) 204–224 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Biogeography and diversification of Brassicales: A 103 million year tale ⇑ Warren M. Cardinal-McTeague a,1, Kenneth J. Sytsma b, Jocelyn C. Hall a, a Department of Biological Sciences, University of Alberta, Edmonton, Alberta T6G 2E9, Canada b Department of Botany, University of Wisconsin, Madison, WI 53706, USA article info abstract Article history: Brassicales is a diverse order perhaps most famous because it houses Brassicaceae and, its premier mem- Received 22 July 2015 ber, Arabidopsis thaliana. This widely distributed and species-rich lineage has been overlooked as a Revised 24 February 2016 promising system to investigate patterns of disjunct distributions and diversification rates. We analyzed Accepted 25 February 2016 plastid and mitochondrial sequence data from five gene regions (>8000 bp) across 151 taxa to: (1) Available online 15 March 2016 produce a chronogram for major lineages in Brassicales, including Brassicaceae and Arabidopsis, based on greater taxon sampling across the order and previously overlooked fossil evidence, (2) examine Keywords: biogeographical ancestral range estimations and disjunct distributions in BioGeoBEARS, and (3) determine Arabidopsis thaliana where shifts in species diversification occur using BAMM. The evolution and radiation of the Brassicales BAMM BEAST began 103 Mya and was linked to a series of inter-continental vicariant, long-distance dispersal, and land BioGeoBEARS bridge migration events. North America appears to be a significant area for early stem lineages in the Brassicaceae order. Shifts to Australia then African are evident at nodes near the core Brassicales, which diverged Cleomaceae 68.5 Mya (HPD = 75.6–62.0). -
Integrated Pest and Crop Management Newsletter, April 2016
Integrated Pest Management April 2016 Integrated Pest & Crop Management Optimum Corn Planting Depth - “Don’t Plant Your Corn Too Shallow” by Gregory Luce There are a lot of factors that influence corn stand and final yield. Some we cannot control and some we can. One easy way to give your corn crop the best opportunity for consistent stand level, and ultimately yield potential, is to plant at the proper depth. The old rule of thumb (index finger in this case) is to plant corn seed at a depth equal to the second knuckle on their index finger. Well, not everybody has the same length fingers so a bit more accurate measurement is in order for this important management decision. University Extension publications across the Midwest typically recommend a corn seeding depth of 1.5 to 2.5 inches. Most agronomists will agree that planting Rootless corn can result if planting corn too shallow. corn too shallow leads to more frequent problems than planting too deep. From my experiences, bad things The second reason for the recommended planting happen when corn seed is planted shallower than 1.5 depth is to establish a strong nodal root system.The inches. Therefore, I recommend targeting 2 inches as nodal root system not only helps support the corn an excellent depth for corn planting. plant structurally, but is also responsible for uptake A primary reason to target a 2 inch depth is to achieve of the vast majority of the water and nutrients the good seed-to-soil contact. In order to accomplish this plant needs. -
A Chromosome-Scale Reference Genome of Lobularia Maritima, An
Huang et al. Horticulture Research (2020) 7:197 Horticulture Research https://doi.org/10.1038/s41438-020-00422-w www.nature.com/hortres ARTICLE Open Access A chromosome-scale reference genome of Lobularia maritima, an ornamental plant with high stress tolerance Li Huang1,YazhenMa1, Jiebei Jiang1,TingLi1, Wenjie Yang1,LeiZhang1,LeiWu1,LandiFeng1, Zhenxiang Xi1, Xiaoting Xu1, Jianquan Liu 1,2 and Quanjun Hu 1 Abstract Lobularia maritima (L.) Desv. is an ornamental plant cultivated across the world. It belongs to the family Brassicaceae and can tolerate dry, poor and contaminated habitats. Here, we present a chromosome-scale, high-quality genome assembly of L. maritima based on integrated approaches combining Illumina short reads and Hi–C chromosome conformation data. The genome was assembled into 12 pseudochromosomes with a 197.70 Mb length, and it includes 25,813 protein-coding genes. Approximately 41.94% of the genome consists of repetitive sequences, with abundant long terminal repeat transposable elements. Comparative genomic analysis confirmed that L. maritima underwent a species-specific whole-genome duplication (WGD) event ~22.99 million years ago. We identified ~1900 species-specific genes, 25 expanded gene families, and 50 positively selected genes in L. maritima. Functional annotations of these genes indicated that they are mainly related to stress tolerance. These results provide new insights into the stress tolerance of L. maritima, and this genomic resource will be valuable for further genetic improvement of this important ornamental plant. 1234567890():,; 1234567890():,; 1234567890():,; 1234567890():,; Introduction ancestral species, WGDs can also promote reproductive Whole-genome duplication (WGD), or polyploidy, has isolation and thus facilitate speciation13. -
Field Pennycress and Winter Camelina)
Agronomy Publications Agronomy 12-30-2020 Weather and landscape influences on pollinator visitation of flowering winter oilseeds (field pennycress and winter camelina) Frank Forcella University of Minnesota - Twin Cities Swetabh Patel Iowa State University Andrew W. Lenssen Iowa State University, [email protected] Cody Hoerning University of Minnesota - Twin Cities M. Scott Wells University of Minnesota - Twin Cities See next page for additional authors Follow this and additional works at: https://lib.dr.iastate.edu/agron_pubs Part of the Climate Commons, Ecology and Evolutionary Biology Commons, Entomology Commons, and the Plant Sciences Commons The complete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ agron_pubs/693. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Agronomy at Iowa State University Digital Repository. It has been accepted for inclusion in Agronomy Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Weather and landscape influences on pollinator visitation of flowering winter oilseeds (field pennycress and winter camelina) Abstract Flowers of field pennycress (Thlaspi arvsense L.) and winter camelina (Camelina sativa (L.) Crantz.) produce abundant pollen and nectar in early spring and thereby may be valuable for pollinators. Insects observed in field plots of these flowers were classified into seven easily identifiable groups (bumblebee, honeybee, solitary bee, butterfly/moth, beetle, fly and other) and monitored for 2 years at three sites in the Upper Midwest region of the USA. -
Chromosome-Level Thlaspi Arvense Genome Provides New Tools for Translational Research and for a Newly Domesticated Cash Cover Crop of the Cooler Climates
bioRxiv preprint doi: https://doi.org/10.1101/2021.07.30.454478; this version posted August 1, 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. Title: Chromosome-level Thlaspi arvense genome provides new tools for translational research and for a newly domesticated cash cover crop of the cooler climates Adam Nunn1,2, Isaac Rodríguez-Arévalo3,4, Zenith Tandukar5, Katherine Frels5,6, Adrián Contreras-Garrido7, Pablo Carbonell-Bejerano7, Panpan Zhang8,9, Daniela Ramos-Cruz3,4, Katharina Jandrasits3,4, Christa Lanz7, Anthony Brusa5, Marie Mirouze8,9, Kevin Dorn10,11, Brice Jarvis12, John Sedbrook12, Donald L. Wyse5, Christian Otto1, David Langenberger1, Peter F. Stadler2,13, Detlef Weigel7, M. David Marks10, James A. Anderson5, Claude Becker3,4,*, Ratan Chopra5,10,* Affiliations 1ecSeq Bioinformatics GmbH, 04103 Leipzig, Germany 2Department of Computer Science, Leipzig University, 04107 Leipzig, Germany 3Genetics, Faculty of Biology, Ludwig Maximilians University, 82152 Martinsried, Germany 4Gregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences (ÖAW), Vienna BioCenter (VBC), 1030 Vienna, Austria 5Department of Agronomy and Plant Genetics, University of Minnesota, Saint Paul, MN, USA 6Department of Agronomy and Horticulture, University of Nebraska, Lincoln, NE, USA 7Department of Molecular Biology, Max Planck Institute -
Cabbage Family Affairs: the Evolutionary History of Brassicaceae
Review Cabbage family affairs: the evolutionary history of Brassicaceae Andreas Franzke1, Martin A. Lysak2, Ihsan A. Al-Shehbaz3, Marcus A. Koch4 and Klaus Mummenhoff5 1 Heidelberg Botanic Garden, Centre for Organismal Studies Heidelberg, Heidelberg University, D-69120 Heidelberg, Germany 2 Department of Functional Genomics and Proteomics, Faculty of Science, Masaryk University, and CEITEC, CZ-625 00 Brno, Czech Republic 3 Missouri Botanical Garden, St. Louis, MO 63166-0299, USA 4 Biodiversity and Plant Systematics, Centre for Organismal Studies Heidelberg, Heidelberg University, D-69120 Heidelberg, Germany 5 Biology Department, Botany, Osnabru¨ ck University, D-49069 Osnabru¨ ck, Germany Life without the mustard family (Brassicaceae) would Glossary be a world without many crop species and the model Adh: alcohol dehydrogenase gene (nuclear genome). organism Arabidopsis (Arabidopsis thaliana) that has Calibration: converting genetic distances to absolute times by means of fossils revolutionized our knowledge in almost every field of or nucleotide substitution rates. modern plant biology. Despite this importance, research Chs: chalcone synthase gene (nuclear genome). Clade: group of organisms (species, genera, etc.) derived from a common breakthroughs in understanding family-wide evolution- ancestor. ary patterns and processes within this flowering plant Core Brassicaceae: all recent lineages except tribe Aethionemeae. family were not achieved until the past few years. In this Crown group age: age of the clade that includes all recent taxa of a group. Evo–devo (evolutionary developmental biology): compares underlying devel- review, we examine recent outcomes from diverse bo- opmental processes of characters in different organisms to investigate the links tanical disciplines (taxonomy, systematics, genomics, between evolution and development. paleobotany and other fields) to synthesize for the first Gamosepaly: fusion of sepals. -
Research on Spontaneous and Subspontaneous Flora of Botanical Garden "Vasile Fati" Jibou
Volume 19(2), 176- 189, 2015 JOURNAL of Horticulture, Forestry and Biotechnology www.journal-hfb.usab-tm.ro Research on spontaneous and subspontaneous flora of Botanical Garden "Vasile Fati" Jibou Szatmari P-M*.1,, Căprar M. 1 1) Biological Research Center, Botanical Garden “Vasile Fati” Jibou, Wesselényi Miklós Street, No. 16, 455200 Jibou, Romania; *Corresponding author. Email: [email protected] Abstract The research presented in this paper had the purpose of Key words inventory and knowledge of spontaneous and subspontaneous plant species of Botanical Garden "Vasile Fati" Jibou, Salaj, Romania. Following systematic Jibou Botanical Garden, investigations undertaken in the botanical garden a large number of spontaneous flora, spontaneous taxons were found from the Romanian flora (650 species of adventive and vascular plants and 20 species of moss). Also were inventoried 38 species of subspontaneous plants, adventive plants, permanently established in Romania and 176 vascular plant floristic analysis, Romania species that have migrated from culture and multiply by themselves throughout the garden. In the garden greenhouses were found 183 subspontaneous species and weeds, both from the Romanian flora as well as tropical plants introduced by accident. Thus the total number of wild species rises to 1055, a large number compared to the occupied area. Some rare spontaneous plants and endemic to the Romanian flora (Galium abaujense, Cephalaria radiata, Crocus banaticus) were found. Cultivated species that once migrated from culture, accommodated to environmental conditions and conquered new territories; standing out is the Cyrtomium falcatum fern, once escaped from the greenhouses it continues to develop on their outer walls. Jibou Botanical Garden is the second largest exotic species can adapt and breed further without any botanical garden in Romania, after "Anastasie Fătu" care [11]. -
Phylogenetic Distribution and Identification of Fin-Winged Fruits
Bot. Rev. (2010) 76:1–82 DOI 10.1007/s12229-010-9041-0 Phylogenetic Distribution and Identification of Fin-winged Fruits Steven R. Manchester1,2 & Elizabeth L. O’Leary1 1 Florida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800, USA 2 Author for Correspondence; e-mail: [email protected] Published online: 9 March 2010 # The New York Botanical Garden 2010 Abstract Fin-winged fruits have two or more wings aligned with the longitudinal axis like the feathers of an arrow, as exemplified by Combretum, Halesia,andPtelea. Such fruits vary in dispersal mode from those in which the fruit itself is the ultimate disseminule, to schizocarps dispersing two or more mericarps, to capsules releasing multiple seeds. At least 45 families and more than 140 genera are known to possess fin-winged fruits. We present an inventory of these taxa and describe their morphological characters as an aid for the identification and phylogenetic assessment of fossil and extant genera. Such fruits are most prevalent among Eudicots, but occur occasionally in Magnoliids (Hernandiaceae: Illigera) and Monocots (Burmannia, Dioscorea, Herreria). Although convergent in general form, fin-winged fruits of different genera can be distinguished by details of the wing number, texture, shape and venation, along with characters of persistent floral parts and dehiscence mode. Families having genera with fin-winged fruits and epigynous perianth include Aizoaceae, Apiaceae, Araliaceae, Asteraceae, Begoniaceae, Burmanniaceae, Combre- taceae, Cucurbitaceae, Dioscoreaceae, Haloragaceae, Lecythidiaceae, Lophopyxida- ceae, Loranthaceae, and Styracaceae. Families with genera having fin-winged fruits and hypogynous perianth include Achariaceae, Brassicaceae, Burseraceae, Celastra- ceae, Cunoniaceae, Cyrillaceae, Fabaceae, Malvaceae, Melianthaceae, Nyctaginaceae, Pedaliaceae, Polygalaceae, Phyllanthaceae, Polygonaceae, Rhamnaceae, Salicaceae sl, Sapindaceae, Simaroubaceae, Trigoniaceae, and Zygophyllaceae.