Fritillaria Imperialis Hybrids) FIRST THINGS FIRST
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Survey for Special-Status Vascular Plant Species
SURVEY FOR SPECIAL-STATUS VASCULAR PLANT SPECIES For the proposed Eagle Canyon Fish Passage Project Tehama and Shasta Counties, California Prepared for: Tehama Environmental Solutions 910 Main Street, Suite D Red Bluff, California 96080 Prepared by: Dittes & Guardino Consulting P.O. Box 6 Los Molinos, California 96055 (530) 384-1774 [email protected] Eagle Canyon Fish Passage Improvement Project - Botany Report Sept. 12, 2018 Prepared by: Dittes & Guardino Consulting 1 SURVEY FOR SPECIAL-STATUS VASCULAR PLANT SPECIES Eagle Canyon Fish Passage Project Shasta & Tehama Counties, California T30N, R1W, SE 1/4 Sec. 25, SE1/4 Sec. 24, NE ¼ Sec. 36 of the Shingletown 7.5’ USGS Topographic Quadrangle TABLE OF CONTENTS I. Executive Summary ................................................................................................................................................. 4 II. Introduction ............................................................................................................................................................ 4 III. Project Description ............................................................................................................................................... 4 IV. Location .................................................................................................................................................................. 5 V. Methods .................................................................................................................................................................. -
Bulb Dormancy in Vitro—Fritillaria Meleagris: Initiation, Release and Physiological Parameters
plants Review Bulb Dormancy In Vitro—Fritillaria meleagris: Initiation, Release and Physiological Parameters Marija Markovi´c*, Milana Trifunovi´cMomˇcilov , Branka Uzelac , Sladana¯ Jevremovi´c and Angelina Suboti´c Department of Plant Physiology, Institute for Biological Research “Siniša Stankovi´c“—NationalInstitute of the Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11060 Belgrade, Serbia; [email protected] (M.T.M.); [email protected] (B.U.); [email protected] (S.J.); [email protected] (A.S.) * Correspondence: [email protected] Abstract: In ornamental geophytes, conventional vegetative propagation is not economically feasible due to very slow development and ineffective methods. It can take several years until a new plant is formed and commercial profitability is achieved. Therefore, micropropagation techniques have been developed to increase the multiplication rate and thus shorten the multiplication and regeneration period. The majority of these techniques rely on the formation of new bulbs and their sprouting. Dormancy is one of the main limiting factors to speed up multiplication in vitro. Bulbous species have a period of bulb dormancy which enables them to survive unfavorable natural conditions. Bulbs grown in vitro also exhibit dormancy, which has to be overcome in order to allow sprouting of bulbs in the next vegetation period. During the period of dormancy, numerous physiological processes occur, many of which have not been elucidated yet. Understanding the process of dormancy will allow us to speed up and improve breeding of geophytes and thereby achieve economic profitability, which is very important for horticulture. This review focuses on recent findings in the area of Citation: Markovi´c,M.; Momˇcilov, bulb dormancy initiation and release in fritillaries, with particular emphasis on the effect of plant M.T.; Uzelac, B.; Jevremovi´c,S.; growth regulators and low-temperature pretreatment on dormancy release in relation to induction of Suboti´c,A. -
Karyological Studies of Fritillaria (Liliaceae) Species from Iran
© 2016 The Japan Mendel Society Cytologia 81(2): 133–141 Karyological Studies of Fritillaria (Liliaceae) Species from Iran Marzieh Ahmadi-Roshan1, Ghasem Karimzadeh1*, Alireza Babaei2 and Hadi Jafari2 1 Department of Plant Breeding and Biotechnology, Faculty of Agriculture, Tarbiat Modares University, Tehran P. O. Box 14115–336, Iran 2 Department of Horticultural Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran Received September 26, 2015; accepted March 14, 2016 Summary Five species (13 ecotypes) belonging to three subgenera of ornamental-medicinal Iranian Fritillaria were karyotypically studied, using a standard squash technique. All species were diploid (2n=2x=24) having mean chromosome lengths of 15.8 µm (15.2–16.7 µm). Their satellites varied in number (1–3 pairs) and in size (1.2–2.6 µm), mostly being located on long arms. Four chromosome types (“m”, “sm”, “st”, “T”) formed 10 dif- ferent karyotype formulas: “T” type chromosome is reported for the first time in most species (with the exception of S4, Fritillaria. reuteri Boissi). ANOVA confirmed significant intra- and inter-specific chromosomal variation across the Iranian Fritillaria species. Twelve different methods were used to assess the degree of karyotype asymmetry. Among those, one qualitative parameter (Stebbins classification) and eight quantitative (CVTL, DI, A1 & A2, AI, A, AsK%, MCA, CVCI) parameters verified that S2 (F. gibbosa Boiss.) and S5 (F. zagrica Stapf.) species represented the most asymmetrical and symmetrical karyotypes, respectively. Key words Fritillaria, Cytogenetics, New chromosome type, Karyotype, Iran. The name Fritillaria is likely based on the word “fri- Fritillaria subgenus is morphologically classified into six tullus” which means a cup in Latin (Ulug et al. -
Analysis of the Giant Genomes of Fritillaria (Liliaceae) Indicates That a Lack of DNA Removal Characterizes Extreme Expansions in Genome Size
CORE Metadata, citation and similar papers at core.ac.uk Provided by Queen Mary Research Online Analysis of the giant genomes of Fritillaria (Liliaceae) indicates that a lack of DNA removal characterizes extreme expansions in genome size. Kelly, LJ; Renny-Byfield, S; Pellicer, J; Macas, J; Novák, P; Neumann, P; Lysak, MA; Day, PD; Berger, M; Fay, MF; Nichols, RA; Leitch, AR; Leitch, IJ © 2015 The Authors. CC-BY For additional information about this publication click this link. http://qmro.qmul.ac.uk/jspui/handle/123456789/8496 Information about this research object was correct at the time of download; we occasionally make corrections to records, please therefore check the published record when citing. For more information contact [email protected] Research Analysis of the giant genomes of Fritillaria (Liliaceae) indicates that a lack of DNA removal characterizes extreme expansions in genome size Laura J. Kelly1,2, Simon Renny-Byfield1,3, Jaume Pellicer2,Jirı Macas4, Petr Novak4, Pavel Neumann4, Martin A. Lysak5, Peter D. Day1,2, Madeleine Berger2,6,7, Michael F. Fay2, Richard A. Nichols1, Andrew R. Leitch1 and Ilia J. Leitch2 1School of Biological and Chemical Sciences, Queen Mary University of London, London, E1 4NS, UK; 2Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, TW9 3DS, UK; 3 4 Department of Plant Sciences, University of California Davis, Davis, CA 95616, USA; Biology Centre CAS, Institute of Plant Molecular Biology, CZ-37005, Ceske Budejovice, Czech Republic; 5Plant Cytogenomics Research Group, CEITEC – Central European Institute of Technology, Masaryk University, Kamenice 5, CZ-62500, Brno, Czech Republic; 6School of Biological and Biomedical Sciences, Durham University, South Road, Durham DH1 3LE, UK; 7Rothamsted Research, West Common, Harpenden, Hertfordshire, AL5 2JQ, UK Summary Authors for correspondence: Plants exhibit an extraordinary range of genome sizes, varying by > 2000-fold between the Laura J. -
Pollen Morphology of Some Fritillaria L. Species (Liliaceae) from Iran
Pak. J. Bot., 50(6): 2311-2315, 2018. POLLEN MORPHOLOGY OF SOME FRITILLARIA L. SPECIES (LILIACEAE) FROM IRAN SHAHLA HOSSEINI Department of Biological Science, University of Kurdistan, P.O. Box 416, Sanandaj, Iran Corresponding author’s email: [email protected] Abstract Pollen grains of 5 taxa from the genus Fritillaria L. in Iran were studied by scanning electron microscopy. Detailed pollen morphological features are given for these taxa. Pollens were monosulcate and ellipsoidal. Sulcus extends from distal to proximal in all studied taxa. Results shows that the sculpturing of the exine, pollen membrane ornamentation and lumina shape provides valuable characters for separating species. Based on these characters, 3 main pollen types were determined with three different exine sculpturing: reticulate, reticulate-perforate and suprareticulate. Key words: Fritillaria, Liliaceae, Pollen morphology, SEM. Introduction Natural Resources. Information about localities of investigated specimens have been provided in table 1. Genus Fritillaria L. (Liliaceae) comprises of For SEM after acetolysis, pollen grains were soaked in approximately 170 taxa (130-140 species) which are absolute ethanol, and were pipetted directly onto 12.5 distributed through the temperate regions of the northern mm diameter stubs, air-dried at room temperature, then hemisphere (Day et al., 2014; Metin et al., 2013). Most of coated in a sputter coater with approximately 25 nm of the species in this genus are belong to the main subgenus, Gold Palladium. The specimens were examined and Fritillaria (Rix et al., 2001). The Mediterranean region is photographed with a TESCAN MIRA 3 scanning the center of genetic diversity of Fritillaria species, with electron microscope. -
Gentner's Fritillary
Gentner’s Fritillary The Discovery and Protection of a Rare Species Georgie Robinett Freedom Plaza 5524, 13373 Plaza del Rio Blvd., Peoria, AZ 85381 are plants are often accidentally discovered. Sometimes amateurs Rfind them. Fritillaria gentneri was first noticed in the spring of 1942, while 18-year-old Laura Gentner was pursuing one of her favorite pastimes, bicycling the back roads of Jackson County. Her bicycle gave her an excellent vantage point for admiring the wildflowers she sometimes collected for her parents’ garden in Med- ford. From this trip, however, she brought home a fritillary unlike the two she was accustomed to seeing on her wildflower jaunts, Fritillaria recurva and F. affinis (historically also known as F. lanceolata). The following spring Laura could not find the new fritillary again. However, the year after that (1944), Laura’s sister Kath- erine recognized it in a bouquet of wild- flowers a friend had picked. Before long, the source was traced to a location south of the town of Jacksonville, about seven miles away. Laura and Katherine’s father, Dr. Louis G. Gentner, was an entomologist who had imbued his family with a deep interest in natural history. His wife Lillian was a horticulturist, and the family en- thusiastically investigated the flora and fauna of Jackson and Josephine counties. Their excitement in discovering what might be a new, undescribed wildflower can be imagined. Dr. Gentner, the Assistant Superin- tendent for the Southern Oregon Branch Fritillaria gentneri: 1, flowering stalk; 2, cross-section of flower; 3, pistil; 4, capsule; 5, outer perianth Experiment Station in Medford, was a segment, face view. -
Flowering Bulbs for Tennessee Gardens
Agricultural Extension Service The University of Tennessee PB 1610 Flowering Bulbs for Tennessee Gardens 1 Contents Bulbs ........................................3 Corms .......................................3 Tubers .......................................3 Rhizomes .....................................4 Culture ......................................4 Introduction ................................4 Site Selection ................................5 Site Preparation ..............................5 Selecting Plant Material ........................5 Planting Spring-Flowering Geophytes ................6 Iris .......................................6 Planting Summer-Flowering Geophytes ..............7 Caladium ..................................7 Canna .....................................8 Dahlia .....................................8 Gladiolus ..................................9 Maintenance of Geophytes ....................... 10 Forcing Spring-Flowering Geophytes in the Home ... 11 Forcing Tender Geophytes in the Home ........... 12 Amaryllis ................................. 12 Dictionary of Bulbous Plants ...................... 13 The Bulb Selector .............................. 21 Mail Order Sources ............................ 22 U.S.D.A. Hardiness Zone Map .................... 23 2 Flowering Bulbs for Tennessee Gardens Mary Lewnes Albrecht, Professor and Head Ornamental Horticulture and Landscape Design wealth of spring-, are thick, fleshy, modified corm does not summer- and fall- leaves, the scales. The scales persist from A flowering -
Spring Flowering Bulbs Anne M
G1742 Spring Flowering Bulbs Anne M. Streich, Extension Educator Don E. Janssen, Extension Educator Kathleen P. Cue, Extension Associate thrive in heavy, constant shade. If reliable bloom is desired Selecting, planting, caring for, harvesting and from year to year, the site should receive at least eight hours forcing spring flowering bulbs are discussed in this of full sunlight per day. Some areas near trees may receive publication. full sun early in the season, before leaves have fully emerged and may be suitable for early flowering bulbs. All bulbs need well-drained soil to reduce rot while dormant. For this reason, Bulbs are underground stems formed by fleshy scales at- areas that receive frequent moisture from lawn irrigation are tached to a basal plate (for example: tulip, narcissus and lily). not desirable planting sites. Corms are underground swollen stems surrounded by dry, Spring flowering bulbs may be used to provide early scale-like leaves (gladiolus, freesia and crocus). Tubers are season color in the landscape while other plants are slowly swollen underground stems that are often irregularly shaped developing. Some, such as grape hyacinths (Figure 1) and (dahlia, gloriosa and ranunculus). Rhizomes are horizontally daffodils (Figure 2), can be planted in grassy areas and may creeping underground stems that produce aerial shoots from spread or multiply to give a naturalized effect. nodes (iris and convallaria). In this publication, all corms, Bulbs planted in a southern exposure near a building or tubers and rhizomes will be referred to as bulbs. wall will encourage early foliage growth due to increased Most spring flowering bulbs are hardy perennials. -
Diversity of Nectar Amino Acids in the Fritillaria(Liliaceae)
www.nature.com/scientificreports Corrected: Author Correction OPEN Diversity of nectar amino acids in the Fritillaria (Liliaceae) genus: ecological and evolutionary implications Katarzyna Roguz 1*, Andrzej Bajguz 2, Magdalena Chmur2, Agnieszka Gołębiewska2, Agata Roguz3 & Marcin Zych 1* Nectar is considered to be a primary food reward for most pollinators. It mostly contains sugars, but also has amino acids. The signifcance of the concentration and composition of amino acids in nectar is often less understood than that of its volume, sugar concentration and composition. However, there is a trend towards a broader approach in ecological research, which helps to understand nectar properties in an ecological context. The genus Fritillaria, exhibiting great diversity in fower morphology, nectar composition, and dominant pollinators, allows for the possibility to study some of the above. We studied the concentration and composition of amino acids in the nectar of 38 Fritillaria species attracting diferent groups of pollen vectors (bees, fies, passerines, and hummingbirds). The fowers of fritillaries produced nectar with a varying composition and concentration of amino acids. These diferences were mostly associated with the pollinator type. The nectar of passerine bird-pollinated species was rich in amino acids, whereas humming bird-pollinated produced low amino acid nectar. Contrary to previous reports nectar of the insect-pollinated species did not contain a higher amount of proline. Two non-protein amino acids, sarcosine and norvaline, were detected in the foral nectar for the frst time. Nectar is the most crucial foral reward for animal pollinators1. Primarily, it is a sugar solution composed of sucrose, fructose and glucose, in varying proportions. -
Vascular Plant Species Checklist and Rare Plants of Fossil Butte National
Vascular Plant Species Checklist And Rare Plants of Fossil Butte National Monument Physaria condensata by Jane Dorn from Dorn & Dorn (1980) Prepared for the National Park Service Northern Colorado Plateau Network By Walter Fertig Wyoming Natural Diversity Database University of Wyoming PO Box 3381, Laramie, WY 82071 9 October 2000 Table of Contents Page # Introduction . 3 Study Area . 3 Methods . 5 Results . 5 Summary of Plant Inventory Work at Fossil Butte National Monument . 5 Flora of Fossil Butte National Monument . 7 Rare Plants of Fossil Butte National Monument . 7 Other Noteworthy Plant Species from Fossil Butte National Monument . 8 Discussion and Recommendations . 8 Acknowledgments . 10 Literature Cited . 11 Figures, Tables, and Appendices Figure 1. Fossil Butte National Monument . 4 Figure 2. Increase in Number of Plant Species Recorded at Fossil Butte National Monument, 1973-2000 . 9 Table 1. Annotated Checklist of the Vascular Plant Flora of Fossil Butte National Monument . 13 Table 2. Rejected Plant Taxa . 32 Table 3. Potential Vascular Plants of Fossil Butte National Monument . 35 Appendix A. Rare Plants of Fossil Butte National Monument . 41 2 INTRODUCTION The National Park Service established Fossil Butte National Monument in October 1972 to preserve significant deposits of fossilized freshwater fish, aquatic organisms, and plants from the Eocene-age Green River Formation. In addition to fossils, the Monument also preserves a mosaic of 12 high desert and montane foothills vegetation types (Dorn et al. 1984; Jones 1993) and over 600 species of vertebrates and vascular plants (Beetle and Marlow 1974; Rado 1976, Clark 1977, Dorn et al. 1984; Kyte 2000). From a conservation perspective, Fossil Butte National Monument is especially significant because it is one of only two managed areas in the basins of southwestern Wyoming to be permanently protected and managed with an emphasis on maintaining biological processes (Merrill et al. -
Phylogenetics of Liliales
Aliso: A Journal of Systematic and Floristic Botany Volume 22 Issue 1 Article 43 2006 Phylogenetics of Liliales Michael F. Fay Royal Botanic Gardens, Kew Mark W. Chase Royal Botanic Gardens, Kew Nina Rønsted Royal Botanic Gardens, Kew Dion S. Devey Royal Botanic Gardens, Kew Yohan Pillon Royal Botanic Gardens, Kew See next page for additional authors Follow this and additional works at: https://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Fay, Michael F.; Chase, Mark W.; Rønsted, Nina; Devey, Dion S.; Pillon, Yohan; Pires, J. Chris; Peterson, Gitte; Seberg, Ole; and Davis, Jerrold I. (2006) "Phylogenetics of Liliales," Aliso: A Journal of Systematic and Floristic Botany: Vol. 22: Iss. 1, Article 43. Available at: https://scholarship.claremont.edu/aliso/vol22/iss1/43 Phylogenetics of Liliales Authors Michael F. Fay, Mark W. Chase, Nina Rønsted, Dion S. Devey, Yohan Pillon, J. Chris Pires, Gitte Peterson, Ole Seberg, and Jerrold I. Davis This article is available in Aliso: A Journal of Systematic and Floristic Botany: https://scholarship.claremont.edu/ aliso/vol22/iss1/43 Liliales MONOCOTS Comparative Biology and Evolution Excluding Poales Aliso 22, pp. 559-565 © 2006, Rancho Santa Ana Botanic Garden PHYLOGENETICS OF LILIALES: SUMMARIZED EVIDENCE FROM COMBINED ANALYSES OF FIVE PLASTID AND ONE MITOCHONDRIAL LOCI 1 5 1 1 1 1 2 6 MICHAEL F. FAY, • MARK W. CHASE, NINA R0NSTED, DION S. DEVEY, YOHAN PILLON, J. CHRIS PIRES, • GITTE PETERSEN,3·7 OLE SEBERG,3·7 AND JERROLD I DAVIS4 1lodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK; 2Department of Agronomy, University of Wisconsin, Madison, Wisconsin 53706, USA; 3Botanical Institute, University of Copenhagen, Gothersgade 140, DK-1123 Copenhagen K, Denmark; 4L. -
Oda2004reportfritillariagentneri.Pdf
Developing biogeographically based population introduction protocols for at-risk plant species of the interior valleys of southwestern Oregon: Fritillaria gentneri (Gentner’s fritillary) Limnanthes floccosa ssp. bellingeriana (Bellinger’s meadowfoam) Limnanthes floccosa ssp. grandiflora (big-flowered wooly meadowfoam) Limnanthes floccosa ssp. pumila (dwarf wooly meadowfoam) Limnanthes gracilis var. gracilis (slender meadowfoam) Lomatium cookii (Cook’s desert parsley) Perideridia erythrorhiza (red-rooted yampah) Plagiobothrys hirtus (rough popcorn flower) Ranunculus austro-oreganus (southern Oregon buttercup) Prepared by Rebecca Currin, Kelly Amsberry, and Robert J. Meinke Native Plant Conservation Program, Oregon Department of Agriculture for U.S. Fish and Wildlife Service (Grant OR-EP-2, segment 14) Acknowledgements: We would like to thank the many people who contributed to the completion of this report. Thanks to Andy Robinson and Kathy Pendergrass (USFWS) for providing funding and encouragement (Grant no. OR-EP-2, segment 14). R.J. Meinke contributed to text completion and review, and Melissa Carr provided invaluable assistance in compiling data. Thanks also to the staff, interns and students who provided plant and habitat photos. Contact Information: Robert J. Meinke Kelly Amsberry Native Plant Conservation Program Native Plant Conservation Program Oregon Department of Agriculture Oregon Department of Agriculture Dept. of Botany and Plant Pathology Dept. of Botany and Plant Pathology Oregon State University Oregon State University Corvallis, OR 97331 Corvallis, OR 97331 (541) 737-2317 (541) 737-4333 [email protected] [email protected] Report format: The following species are presented in alphabetical order: Fritillaria gentneri (Gentner’s fritillary), Limnanthes floccosa ssp. bellingeriana (Bellinger’s meadowfoam), Limnanthes floccosa ssp. grandiflora (big-flowered wooly meadowfoam), Limnanthes floccosa ssp.