North American Rock Garden Society |
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Phylogeny and Evolution of the Arctium-Cousinia Complex (Compositae, Cardueae-Carduinae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC TAXON 58 (1) • February 2009: 153–171 López-Vinyallonga & al. • Arctium-Cousinia complex Phylogeny and evolution of the Arctium-Cousinia complex (Compositae, Cardueae-Carduinae) Sara López-Vinyallonga1,4*, Iraj Mehregan2,4, Núria Garcia-Jacas1, Olga Tscherneva3, Alfonso Susanna1 & Joachim W. Kadereit2 1 Botanical Institute of Barcelona (CSIC-ICUB), Pg. del Migdia s. n., 08038 Barcelona, Spain. *slopez@ibb. csic.es (author for correspondence) 2 Johannes Gutenberg-Universität Mainz, Institut für Spezielle Botanik und Botanischer Garten, 55099 Mainz, Germany 3 Komarov Botanical Institute, Ul. Prof. Popova 2, 197376 St. Petersburg, Russia 4 These authors contributed equally to this publication The phylogeny and evolution of the Arctium-Cousinia complex, including Arctium, Cousinia as one of the largest genera of Asteraceae, Hypacanthium and Schmalhausenia, is investigated. This group of genera has its highest diversity in the Irano-Turanian region and the mountains of Central Asia. We generated ITS and rpS4-trnT-trnL sequences for altogether 138 species, including 129 (of ca. 600) species of Cousinia. As found in previous analyses, Cousinia is not monophyletic. Instead, Cousinia subgg. Cynaroides and Hypacanthodes with together ca. 30 species are more closely related to Arctium, Hypacanthium and Schmalhausenia (Arc- tioid clade) than to subg. Cousinia (Cousinioid clade). The Arctioid and Cousiniod clades are also supported by pollen morphology and chromosome number as reported earlier. In the Arctioid clade, the distribution of morphological characters important for generic delimitation, mainly leaf shape and armature and morphology of involucral bracts, are highly incongruent with phylogenetic relationships as implied by the molecular data. -
Appendix Color Plates of Solanales Species
Appendix Color Plates of Solanales Species The first half of the color plates (Plates 1–8) shows a selection of phytochemically prominent solanaceous species, the second half (Plates 9–16) a selection of convol- vulaceous counterparts. The scientific name of the species in bold (for authorities see text and tables) may be followed (in brackets) by a frequently used though invalid synonym and/or a common name if existent. The next information refers to the habitus, origin/natural distribution, and – if applicable – cultivation. If more than one photograph is shown for a certain species there will be explanations for each of them. Finally, section numbers of the phytochemical Chapters 3–8 are given, where the respective species are discussed. The individually combined occurrence of sec- ondary metabolites from different structural classes characterizes every species. However, it has to be remembered that a small number of citations does not neces- sarily indicate a poorer secondary metabolism in a respective species compared with others; this may just be due to less studies being carried out. Solanaceae Plate 1a Anthocercis littorea (yellow tailflower): erect or rarely sprawling shrub (to 3 m); W- and SW-Australia; Sects. 3.1 / 3.4 Plate 1b, c Atropa belladonna (deadly nightshade): erect herbaceous perennial plant (to 1.5 m); Europe to central Asia (naturalized: N-USA; cultivated as a medicinal plant); b fruiting twig; c flowers, unripe (green) and ripe (black) berries; Sects. 3.1 / 3.3.2 / 3.4 / 3.5 / 6.5.2 / 7.5.1 / 7.7.2 / 7.7.4.3 Plate 1d Brugmansia versicolor (angel’s trumpet): shrub or small tree (to 5 m); tropical parts of Ecuador west of the Andes (cultivated as an ornamental in tropical and subtropical regions); Sect. -
BIGHEAD KNAPWEED (Centaurea Macrocephala Puschk.)
PNW386 BIGHEAD KNAPWEED (Centaurea macrocephala Puschk.) Bighead knapweed is native to woody crown, each topped by a the mountain grasslands of 3-inch flower head. When Caucasia (specifically Armenia competing with other plants, and Romania) and also to bighead knapweed is generally subalpine meadows in Turkey. only 2 to 3 feet tall with one or European growers cultivate it as two stalks bearing flower heads an ornamental flower and sell it about 1.5 inches in diameter. in the fresh flower markets. Broadly lance-shaped leaves have Although not as popular as sharp-pointed tips, shallowly cornflower (bachelor's button) or toothed edges and rough mountain bluet, it is also surfaces. Blades of the stalked available in the United States in basal and rosette leaves may be flower seed catalogs and 10 inches long and 3 inches wide; nurseries under various common blade and stalk together may names, including Lemon fluff exceed 15 inches. Stem leaves and Globe Centaury. gradually change from having Occasionally, it appears in dried simple stalks to winged stalks to flower arrangements. stalkless as they become smaller Weed specialists in Washington going up the stem. The smallest found bighead knapweed in the Under frroorable conditions, bighead leaves are clustered on the early 1980s escaping from knapweed grows 4 to 5 feet tall. (Each swollen stem at the base of the abandoned gardens in Pend stripe on the stake is 4 inches.) flower head. Oreille and Whitman counties, and added it to the Class A noxious weed list. Since then, Okanogan County, Washington, and Quesnel, British Columbia have reported it. -
Approaches and Limitations of Species Level Diagnostics in Flowering Plants
Genetic Food Diagnostics Approaches and Limitations of Species Level Diagnostics in Flowering Plants Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN (Dr. rer. nat.) Fakultät für Chemie und Biowissenschaften Karlsruher Institut für Technologie (KIT) - Universitätsbereich genehmigte DISSERTATION von Dipl. Biologe Thomas Horn aus 77709 Wolfach Dekan: Prof. Dr. Peter Roesky Referent: Prof. Dr. Peter Nick Korreferent: Prof. Dr. Horst Taraschewski Tag der mündlichen Prüfung: 17.04.2014 Parts of this work are derived from the following publications: Horn T, Völker J, Rühle M, Häser A, Jürges G, Nick P; 2013; Genetic authentication by RFLP versus ARMS? The case of Moldavian Dragonhead (Dracocephalum moldavica L.). European Food Research and Technology, doi 10.1007/s00217-013-2089-4 Horn T, Barth A, Rühle M, Häser A, Jürges G, Nick P; 2012; Molecular Diagnostics of Lemon Myrtle (Backhousia citriodora versus Leptospermum citratum). European Food Research and Technology, doi 10.1007/s00217-012-1688-9 Also included are works from the following teaching projects: RAPD Analysis and SCAR design in the TCM complex Clematis Armandii Caulis (chuān mù tōng), F2 Plant Evolution, 2011 Effects of highly fragmented DNA on PCR, F3, Lidija Krebs, 2012 1 I. Acknowledgement “Nothing is permanent except change” Heraclitus of Ephesus Entering adolescence – approximately 24 years ago – many aspects of life pretty much escaped my understanding. After a period of turmoil and subsequent experience of a life as laborer lacking an education, I realized that I did not want to settle for this kind of life. I wanted to change. With this work I would like to thank all people that ever bothered trying to explain the world to me, that allowed me to find my way and nurtured my desire to change. -
Plant Species of Special Concern and Vascular Plant Flora of the National
Plant Species of Special Concern and Vascular Plant Flora of the National Elk Refuge Prepared for the US Fish and Wildlife Service National Elk Refuge By Walter Fertig Wyoming Natural Diversity Database The Nature Conservancy 1604 Grand Avenue Laramie, WY 82070 February 28, 1998 Acknowledgements I would like to thank the following individuals for their assistance with this project: Jim Ozenberger, ecologist with the Jackson Ranger District of Bridger-Teton National Forest, for guiding me in his canoe on Flat Creek and for providing aerial photographs and lodging; Jennifer Whipple, Yellowstone National Park botanist, for field assistance and help with field identification of rare Carex species; Dr. David Cooper of Colorado State University, for sharing field information from his 1994 studies; Dr. Ron Hartman and Ernie Nelson of the Rocky Mountain Herbarium, for providing access to unmounted collections by Michele Potkin and others from the National Elk Refuge; Dr. Anton Reznicek of the University of Michigan, for confirming the identification of several problematic Carex specimens; Dr. Robert Dorn for confirming the identification of several vegetative Salix specimens; and lastly Bruce Smith and the staff of the National Elk Refuge for providing funding and logistical support and for allowing me free rein to roam the refuge for plants. 2 Table of Contents Page Introduction . 6 Study Area . 6 Methods . 8 Results . 10 Vascular Plant Flora of the National Elk Refuge . 10 Plant Species of Special Concern . 10 Species Summaries . 23 Aster borealis . 24 Astragalus terminalis . 26 Carex buxbaumii . 28 Carex parryana var. parryana . 30 Carex sartwellii . 32 Carex scirpoidea var. scirpiformis . -
<I>Carthamus Tinctorius</I>
Promoting the conservation and use of underutilized and neglected crops. 7. SafflowerSafflower Carthamus tinctorius L. Li Dajue and Hans-Henning Mündel netic t Ge Res lan ou P rc al e n s o I ti n a s t n i r t u e t t e n I IPGRI 2 Safflower. Carthamus tinctorius L. The International Plant Genetic Resources Institute (IPGRI) is an autonomous inter- national scientific organization operating under the aegis of the Consultative Group on International Agricultural Research (CGIAR). The international status of IPGRI is conferred under an Establishment Agreement which, by December 1995, had been signed by the Governments of Australia, Belgium, Benin, Bolivia, Burkina Faso, Cameroon, China, Chile, Congo, Costa Rica, Côte d’Ivoire, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Greece, Guinea, Hungary, India, Iran, Israel, Italy, Jordan, Kenya, Mauritania, Morocco, Pakistan, Panama, Peru, Poland, Portugal, Romania, Russia, Senegal, Slovak Republic, Sudan, Switzerland, Syria, Tunisia, Turkey, Ukraine and Uganda. IPGRI’s mandate is to advance the conservation and use of plant genetic resources for the benefit of present and future generations. IPGRI works in partner- ship with other organizations, undertaking research, training and the provision of scientific and technical advice and information, and has a particularly strong programme link with the Food and Agriculture Organization of the United Nations. Financial support for the agreed research agenda of IPGRI is provided by the Gov- ernments of Australia, Austria, Belgium, Canada, China, Denmark, France, Ger- many, India, Italy, Japan, the Republic of Korea, Mexico, the Netherlands, Norway, Spain, Sweden, Switzerland, the UK and the USA, and by the Asian Development Bank, IDRC, UNDP and the World Bank. -
Extensive Chromosomal Variation in a Recently Formed Natural Allopolyploid Species, Tragopogon Miscellus (Asteraceae)
Extensive chromosomal variation in a recently formed natural allopolyploid species, Tragopogon miscellus (Asteraceae) Michael Chestera, Joseph P. Gallaghera, V. Vaughan Symondsb, Ana Veruska Cruz da Silvac,d, Evgeny V. Mavrodievd, Andrew R. Leitche, Pamela S. Soltisd, and Douglas E. Soltisa,1 aDepartment of Biology, University of Florida, Gainesville, FL 32611; bInstitute of Molecular Biosciences, Massey University, Palmerston North, 4442, New Zealand; cEmbrapa Tabuleiros Costeiros, CEP 49025-040, Aracaju-SE, Brazil; dFlorida Museum of Natural History, University of Florida, Gainesville, FL 32611; and eSchool of Biological and Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom Edited by James A. Birchler, University of Missouri, Columbia, MO, and approved December 6, 2011 (received for review July 22, 2011) Polyploidy, or whole genome duplication, has played a major role after whole genome duplication (18). In some cases, the regularity in the evolution of many eukaryotic lineages. Although the of meiosis was found to increase rapidly in experimental neo- prevalence of polyploidy in plants is well documented, the molec- allopolyploids that were initially chromosomally unstable (21, ular and cytological consequences are understood largely from 22); for example, after just five selfed generations, Nicotiana newly formed polyploids (neopolyploids) that have been grown neoallotetraploids displayed bivalent pairing and >99% stainable experimentally. Classical cytological and molecular cytogenetic pollen (22). -
December 2012 Number 1
Calochortiana December 2012 Number 1 December 2012 Number 1 CONTENTS Proceedings of the Fifth South- western Rare and Endangered Plant Conference Calochortiana, a new publication of the Utah Native Plant Society . 3 The Fifth Southwestern Rare and En- dangered Plant Conference, Salt Lake City, Utah, March 2009 . 3 Abstracts of presentations and posters not submitted for the proceedings . 4 Southwestern cienegas: Rare habitats for endangered wetland plants. Robert Sivinski . 17 A new look at ranking plant rarity for conservation purposes, with an em- phasis on the flora of the American Southwest. John R. Spence . 25 The contribution of Cedar Breaks Na- tional Monument to the conservation of vascular plant diversity in Utah. Walter Fertig and Douglas N. Rey- nolds . 35 Studying the seed bank dynamics of rare plants. Susan Meyer . 46 East meets west: Rare desert Alliums in Arizona. John L. Anderson . 56 Calochortus nuttallii (Sego lily), Spatial patterns of endemic plant spe- state flower of Utah. By Kaye cies of the Colorado Plateau. Crystal Thorne. Krause . 63 Continued on page 2 Copyright 2012 Utah Native Plant Society. All Rights Reserved. Utah Native Plant Society Utah Native Plant Society, PO Box 520041, Salt Lake Copyright 2012 Utah Native Plant Society. All Rights City, Utah, 84152-0041. www.unps.org Reserved. Calochortiana is a publication of the Utah Native Plant Society, a 501(c)(3) not-for-profit organi- Editor: Walter Fertig ([email protected]), zation dedicated to conserving and promoting steward- Editorial Committee: Walter Fertig, Mindy Wheeler, ship of our native plants. Leila Shultz, and Susan Meyer CONTENTS, continued Biogeography of rare plants of the Ash Meadows National Wildlife Refuge, Nevada. -
Evaluating the Monophyly and Biogeography of Cryptantha (Boraginaceae)
Systematic Botany (2018), 43(1): pp. 53–76 © Copyright 2018 by the American Society of Plant Taxonomists DOI 10.1600/036364418X696978 Date of publication April 18, 2018 Evaluating the Monophyly and Biogeography of Cryptantha (Boraginaceae) Makenzie E. Mabry1,2 and Michael G. Simpson1 1Department of Biology, San Diego State University, San Diego, California 92182, U. S. A. 2Current address: Division of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211, U. S. A. Authors for correspondence ([email protected]; [email protected]) Abstract—Cryptantha, an herbaceous plant genus of the Boraginaceae, subtribe Amsinckiinae, has an American amphitropical disjunct distri- bution, found in western North America and western South America, but not in the intervening tropics. In a previous study, Cryptantha was found to be polyphyletic and was split into five genera, including a weakly supported, potentially non-monophyletic Cryptantha s. s. In this and subsequent studies of the Amsinckiinae, interrelationships within Cryptantha were generally not strongly supported and sample size was generally low. Here we analyze a greatly increased sampling of Cryptantha taxa using high-throughput, genome skimming data, in which we obtained the complete ribosomal cistron, the nearly complete chloroplast genome, and twenty-three mitochondrial genes. Our analyses have allowed for inference of clades within this complex with strong support. The occurrence of a non-monophyletic Cryptantha is confirmed, with three major clades obtained, termed here the Johnstonella/Albidae clade, the Maritimae clade, and a large Cryptantha core clade, each strongly supported as monophyletic. From these phylogenomic analyses, we assess the classification, character evolution, and phylogeographic history that elucidates the current amphitropical distribution of the group. -
Rubus Arcticus Ssp. Acaulis Is Also Appreciated
Rubus arcticus L. ssp. acaulis (Michaux) Focke (dwarf raspberry): A Technical Conservation Assessment Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project October 18, 2006 Juanita A. R. Ladyman, Ph.D. JnJ Associates LLC 6760 S. Kit Carson Cir E. Centennial, CO 80122 Peer Review Administered by Society for Conservation Biology Ladyman, J.A.R. (2006, October 18). Rubus arcticus L. ssp. acaulis (Michaux) Focke (dwarf raspberry): a technical conservation assessment. [Online]. USDA Forest Service, Rocky Mountain Region. Available: http:// www.fs.fed.us/r2/projects/scp/assessments/rubusarcticussspacaulis.pdf [date of access]. ACKNOWLEDGMENTS The time spent and help given by all the people and institutions mentioned in the reference section are gratefully acknowledged. I would also like to thank the Wyoming Natural Diversity Database, in particular Bonnie Heidel, and the Colorado Natural Heritage Program, in particular David Anderson, for their generosity in making their records available. The data provided by Lynn Black of the DAO Herbarium and National Vascular Plant Identification Service in Ontario, Marta Donovan and Jenifer Penny of the British Columbia Conservation Data Center, Jane Bowles of University of Western Ontario Herbarium, Dr. Kadri Karp of the Aianduse Instituut in Tartu, Greg Karow of the Bighorn National Forest, Cathy Seibert of the University of Montana Herbarium, Dr. Anita Cholewa of the University of Minnesota Herbarium, Dr. Debra Trock of the Michigan State University Herbarium, John Rintoul of the Alberta Natural Heritage Information Centre, and Prof. Ron Hartman and Joy Handley of the Rocky Mountain Herbarium at Laramie, were all very valuable in producing this assessment. -
David A. Rasmussen, 2 Elena M. Kramer, 3 and Elizabeth A. Zimmer 4
American Journal of Botany 96(1): 96–109. 2009. O NE SIZE FITS ALL? M OLECULAR EVIDENCE FOR A COMMONLY INHERITED PETAL IDENTITY PROGRAM IN RANUNCULALES 1 David A. Rasmussen, 2 Elena M. Kramer, 3 and Elizabeth A. Zimmer 4 Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138 USA Petaloid organs are a major component of the fl oral diversity observed across nearly all major clades of angiosperms. The vari- able morphology and development of these organs has led to the hypothesis that they are not homologous but, rather, have evolved multiple times. A particularly notable example of petal diversity, and potential homoplasy, is found within the order Ranunculales, exemplifi ed by families such as Ranunculaceae, Berberidaceae, and Papaveraceae. To investigate the molecular basis of petal identity in Ranunculales, we used a combination of molecular phylogenetics and gene expression analysis to characterize APETALA3 (AP3 ) and PISTILLATA (PI ) homologs from a total of 13 representative genera of the order. One of the most striking results of this study is that expression of orthologs of a single AP3 lineage is consistently petal-specifi c across both Ranunculaceae and Berberidaceae. We conclude from this fi nding that these supposedly homoplastic petals in fact share a developmental genetic program that appears to have been present in the common ancestor of the two families. We discuss the implications of this type of molecular data for long-held typological defi nitions of petals and, more broadly, the evolution of petaloid organs across the angiosperms. Key words: APETALA3 ; MADS box genes; petal evolution; PISTILLATA ; Ranunculales.