Minnesota Dwarf Trout Lily: an Endangered Minnesota Wildflower.” Minnesota Department of Natural Resources, St
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Liliaceae S.L. (Lily Family)
Liliaceae s.l. (Lily family) Photo: Ben Legler Photo: Hannah Marx Photo: Hannah Marx Lilium columbianum Xerophyllum tenax Trillium ovatum Liliaceae s.l. (Lily family) Photo: Yaowu Yuan Fritillaria lanceolata Ref.1 Textbook DVD KRR&DLN Erythronium americanum Allium vineale Liliaceae s.l. (Lily family) Herbs; Ref.2 Stems often modified as underground rhizomes, corms, or bulbs; Flowers actinomorphic; 3 sepals and 3 petals or 6 tepals, 6 stamens, 3 carpels, ovary superior (or inferior). Tulipa gesneriana Liliaceae s.l. (Lily family) “Liliaceae” s.l. (sensu lato: “in the broad sense”) - Lily family; 288 genera/4950 species, including Lilium, Allium, Trillium, Tulipa; This family is treated in a very broad sense in this class, as in the Flora of the Pacific Northwest. The “Liliaceae” s.l. taught in this class is not monophyletic. It is apparent now that the family should be treated in a narrower sense and some of the members should form their own families. Judd et al. recognize 15+ families: Agavaceae, Alliaceae, Amarylidaceae, Asparagaceae, Asphodelaceae, Colchicaceae, Dracaenaceae (Nolinaceae), Hyacinthaceae, Liliaceae, Melanthiaceae, Ruscaceae, Smilacaceae, Themidaceae, Trilliaceae, Uvulariaceae and more!!! (see web reading “Consider the Lilies”) Iridaceae (Iris family) Photo: Hannah Marx Photo: Hannah Marx Iris pseudacorus Iridaceae (Iris family) Photo: Yaowu Yuan Photo: Yaowu Yuan Sisyrinchium douglasii Sisyrinchium sp. Iridaceae (Iris family) Iridaceae - 78 genera/1750 species, Including Iris, Gladiolus, Sisyrinchium. Herbs, aquatic or terrestrial; Underground stems as rhizomes, bulbs, or corms; Leaves alternate, 2-ranked and equitant Ref.3 (oriented edgewise to the stem; Gladiolus italicus Flowers actinomorphic or zygomorphic; 3 sepals and 3 petals or 6 tepals; Stamens 3; Ovary of 3 fused carpels, inferior. -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
The Ustilaginales (Smut Fungi) of Ohio*
THE USTILAGINALES (SMUT FUNGI) OF OHIO* C. W. ELLETT Department of Botany and Plant Pathology, The Ohio State University, Columbus 10 The smut fungi are in the order Ustilaginales with one family, the Ustilaginaceae, recognized. They are all plant parasites. In recent monographs 276 species in 22 genera are reported in North America and more than 1000 species have been reported from the world (Fischer, 1953; Zundel, 1953; Fischer and Holton, 1957). More than one half of the known smut fungi are pathogens of species in the Gramineae. Most of the smut fungi are recognized by the black or brown spore masses or sori forming in the inflorescences, the leaves, or the stems of their hosts. The sori may involve the entire inflorescence as Ustilago nuda on Hordeum vulgare (fig. 2) and U. residua on Danthonia spicata (fig. 7). Tilletia foetida, the cause of bunt of wheat in Ohio, sporulates in the ovularies only and Ustilago violacea which has been found in Ohio on Silene sp. forms spores only in the anthers of its host. The sori of Schizonella melanogramma on Carex (fig. 5) and of Urocystis anemones on Hepatica (fig. 4) are found in leaves. Ustilago striiformis (fig. 6) which causes stripe smut of many grasses has sori which are mostly in the leaves. Ustilago parlatorei, found in Ohio on Rumex (fig. 3), forms sori in stems, and in petioles and midveins of the leaves. In a few smut fungi the spore masses are not conspicuous but remain buried in the host tissues. Most of the species in the genera Entyloma and Doassansia are of this type. -
Alternative Strategies for Clonal Plant Reproduction©
Alternative Strategies for Clonal Plant Reproduction 269 Alternative Strategies for Clonal Plant Reproduction© Robert L. Geneve University of Kentucky, Department of Horticulture, Lexington, Kentucky 40546 U.S.A. Email: [email protected] INTRODUCTION Pick up any biology textbook and there will be a description of the typical sexual life cycle for plants. In higher plants, the life cycle starts with seed germination followed by vegetative growth leading to flower and gamete formation with the ultimate goal of creating genetically diverse offspring through seed production. The fern life cycle is more primitive but follows a similar progression from spore germi- nation to the gametophytic generation leading to sexual union of gametes resulting in the leafy sporophyte, which in turn creates the spores. Interestingly, plants have evolved unique alternative life cycles that bypass typi- cal seed production in favor of clonal reproduction systems. This may seem counter- intuitive because sexual reproduction should lead to greater genetic diversity in offspring compared to clonal plants. These sexual offspring should have a higher potential to adapt to new or changing environments, i.e., be more successful. How- ever, investing in clonal reproduction seems to increase the likelihood that a species can colonize specific environmental niches. It has been observed that many of the perennial species in a given ecosystem tend to combine both sexual and clonal forms of reproduction (Ellstrand and Roose, 1987). Additionally, unique clonal propaga- tion systems tend to be more prevalent in plants adapted to extreme environments like arctic, xerophytic, and Mediterranean climates. Mini-Review Objectives. The objective of this mini-review is to describe some of the ways plants have evolved clonal reproduction strategies that allow unique plants to colonize extreme environments. -
Minnesota Biodiversity Atlas Plant List
Cannon River Trout Lily SNA Plant List Herbarium Scientific Name Minnesota DNR Common Name Status Acer negundo box elder Acer saccharum sugar maple Achillea millefolium common yarrow Adiantum pedatum maidenhair fern Agastache scrophulariaefolia purple giant hyssop Ageratina altissima white snakeroot Agrostis stolonifera spreading bentgrass Allium tricoccum tricoccum wild leek Ambrosia artemisiifolia common ragweed Ambrosia trifida great ragweed Anemone acutiloba sharp-lobed hepatica Anemone quinquefolia quinquefolia wood anemone Anemone virginiana alba tall thimbleweed Antennaria parlinii fallax Parlin's pussytoes Aquilegia canadensis columbine Arctium minus common burdock Arisaema triphyllum Jack-in-the-pulpit Asarum canadense wild ginger Asclepias speciosa showy milkweed Athyrium filix-femina angustum lady fern Barbarea vulgaris yellow rocket Bromus inermis smooth brome Campanula americana tall bellflower Capsella bursa-pastoris shepherd's-purse Cardamine concatenata cut-leaved toothwort Carex cephalophora oval-headed sedge Carex gravida heavy sedge Carex grisea ambiguous sedge Carex rosea starry sedge Carex sprengelii Sprengel's sedge Carex vulpinoidea fox sedge Carya cordiformis bitternut hickory Caulophyllum thalictroides blue cohosh Celtis occidentalis hackberry Cerastium fontanum mouse-ear chickweed Chenopodium album white lamb's quarters Circaea lutetiana canadensis common enchanter's nightshade Cirsium discolor field thistle Cirsium vulgare bull thistle Claytonia virginica Virginia spring beauty Conyza canadensis horseweed © -
ERYTHRONIUMS in CULTIVATION © Ian Young Erythronium Californicum
ERYTHRONIUMS IN CULTIVATION © Ian Young ERYTHRONIUMS IN CULTIVATION © Ian Young Erythronium californicum ERYTHRONIUMS IN CULTIVATION © Ian Young Erythronium californicum Erythronium californicum filaments are narrow, ribbon-like with milky white pollen , the flowers are also creamy white with a yellow centre; some forms have dark red zig zag patterns around the centre. Erythronium californicum is another excellent garden plant which is most often seen under the cultivar name of Erythronium ‘White Beauty’ this is readily available. I include ‘White Beauty’ here, rather than under hybrids, as there are no morphological indications that any other species is involved. What makes this form such a good garden plant is its ability to tolerate a wide range of garden types and increase well by division: a healthy well- grown bulb can make two new flowering sized bulbs plus have several smaller offsets every year – it also regularly sets seed. Erythronium ‘White Beauty’ ERYTHRONIUMS IN CULTIVATION © Ian Young Erythronium californicum All forms are free flowering, setting seed most years provided the weather conditions at flowering time are not too cold and wet. Erythronium ‘White Beauty’ has fewer seeds in the capsule compared to other forms; about one third of the number. Erythronium californicum seeds ERYTHRONIUMS IN CULTIVATION © Ian Young Bulb On the left is a group of Erythronium californicum bulbs showing the typical shape – the longer thin ones are younger bulbs still taking themselves down into the ground seeking the best conditions. Most forms will increase by offsets, soon forming clumps – forms such as ‘White Beauty’ form clumps quickly, see below, and are best lifted and divided every three to five years to maintain good flowering. -
Erythronium Revolutum Sm
Erythronium revolutum Sm. pink fawn-lily Liliaceae - lily family status: State Sensitive rank: G4 / S3 General Description: Perennial from elongate underground bulbs. Leaves basal, paired, strongly mottled with irregular patches of pale green, brown, or white on a dark green background, oblong-lanceolate to broadly elliptic, (9) 12-18 (25) cm long. Floral Characteristics: Flowers 1-3, nodding on a leafless peduncle 1.5-4 dm tall. Tepals 6, 3.5-4 (5) cm long, uniformly deep pink with yellow banding at the base, drying to pinkish purple, spreading to reflexed; the inner with 2-4 saclike appendages near the base. Stamens 6, 12-22 mm. Filaments flattened, 2-3 mm wide, white to pink, darkening with age. A nthers yellow; style 12-18 mm. Stigma 3-lobed, lobes recurved, 4-6 mm. Flowers A pril to May. Fruits: Capsules oblong to club-shaped, 3-6 cm. Identif ication Tips: Erythronium revolutum sometimes hybridizes with E. Illustration by Jeanne R. Janish, oregonum, which has white to creamy white tepals (becoming pinkish in ©1969 University of Washington Press age, sometimes with red lines or bands). E. quinaultense has green or faintly mottled leaves, paler flowers than E. revolutum, and flattened filaments 0.8-2 mm wide. E. elegans is endemic to the O R Coast Range and has cream to white tepals, often strongly marked with pink and aging to deeper pink; its leaves have nearly no mottling. E. quinaultens e is endemic to the O lympic Mts. of WA ; all 6 of its tepals are white below, shading to pink at the outer margins and tips. -
SRGC BULB LOG DIARY---Pictures and Text © Ian Young
SRGC ----- Bulb Log Diary ----- Pictures and text © Ian Young BULB LOG 0 1....................................6th January 2016 Erythroniums in Cultivation chapters - Erythronium grandiflorum and Erythronium tuolumnense A very happy and healthy New Year to all my Bulb Log readers, I hope you also have a great gardening year. I would also like to say a big thank you to Len Rhind who has compiled an index to the Bulb log - updating it every year since the very start. Len very generously shares this work with all of us and you can access and download the latest version here- Bulb Log Index Weather wise 2016 has not got off to a very good start in the UK and especially here in the northeast where we have had constant rain for over a week now. The rain has prevented me from getting on with my normal tasks of winter tree pruning along with tidying and mulching the beds before the spring growth emerges. This small setback is trivial compared to the many people who have suffered flooding of both gardens and homes. I do hope that we get a dry period during January so I can achieve the tidy-up and mulching of the beds at least – the tree work can always be done later. Cyclamen coum The persistent rain clouds also bring the gloom at this time of year and we are in almost darkness all the time so it is very difficult to get any pictures taken. It is at times like this that areas near the house with the troughs and bonsai, this week’s cover picture, show their year round decorative qualities. -
Pollen Morphology of Erythronium L. (Liliaceae) and Its Systematic Relationships
J. Basic. Appl. Sci. Res., 2(2)1833-1838, 2012 ISSN 2090-4304 Journal of Basic and Applied © 2012, TextRoad Publication Scientific Research www.textroad.com Pollen Morphology of Erythronium L. (Liliaceae) and its Systematic Relationships Sayed-Mohammad Masoumi Department of Plant Protection, Razi University, Kermanshah, Iran ABSTRACT Pollen morphology of three genus of Erythronium was studied by the Light Microscopy (LM), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). Sulcus long reaching the ends of the grains, with operculum (E. giganteum, E. sibiricum) or without it (E. caucasicum). With surface latticed ornamentation and large lattice, thickness of muri and size of Lumina in E. sibiricum are widely varied. Also, most palynomorphological characteristics of the data transmission electron microscopy (TEM) showed no strong differences between E. caucasicum and E. sibiricum, , but these species are well distinguished from E. giganteum according to ectexine thickness (thickness of the tectum and the foot layer), shape and diameter of the caput, height and width of the columella. KEY WORDS: Caput; Columella; Exine ornamentation; intine; Microrelief; Pollen grain; Tectum. INTRODUCTION Takhtajan, 1987 indicated that the genus of Erythronium in Tribe Tulipeae is of the Liliaceae family. Different sources have considered the species number of this genus varied from 24-30. Baranova (1999) introduced 24 species for this genus, of which 20 species were spread in North America. Allen et al. (2003) examined the genus of Erythronium, Amana, and Tulipa using the DNA sequences from the chloroplast gene matK and the internal transcribed spacer (ITS) of nuclear ribosomal DNA. Palynomorphological characters of 20 different pollen species of Erythronium were evaluated by different researchers (Ikuse, 1965; Beug (1963); Radulescu, 1973; Nakamura, 1980; Schulze, 1980; Kuprianova, 1983; Takahashi (1987); Kosenko, 1991b, 1992, 1996, 1999; Maassoumi, 2005a, 2005b, 2007). -
Mississippi Natural Heritage Program Special Plants - Tracking List -2018
MISSISSIPPI NATURAL HERITAGE PROGRAM SPECIAL PLANTS - TRACKING LIST -2018- Approximately 3300 species of vascular plants (fern, gymnosperms, and angiosperms), and numerous non-vascular plants may be found in Mississippi. Many of these are quite common. Some, however, are known or suspected to occur in low numbers; these are designated as species of special concern, and are listed below. There are 495 special concern plants, which include 4 non- vascular plants, 28 ferns and fern allies, 4 gymnosperms, and 459 angiosperms 244 dicots and 215 monocots. An additional 100 species are designated “watch” status (see “Special Plants - Watch List”) with the potential of becoming species of special concern and include 2 fern and fern allies, 54 dicots and 44 monocots. This list is designated for the primary purposes of : 1) in environmental assessments, “flagging” of sensitive species that may be negatively affected by proposed actions; 2) determination of protection priorities of natural areas that contain such species; and 3) determination of priorities of inventory and protection for these plants, including the proposed listing of species for federal protection. GLOBAL STATE FEDERAL SPECIES NAME COMMON NAME RANK RANK STATUS BRYOPSIDA Callicladium haldanianum Callicladium Moss G5 SNR Leptobryum pyriforme Leptobryum Moss G5 SNR Rhodobryum roseum Rose Moss G5 S1? Trachyxiphium heteroicum Trachyxiphium Moss G2? S1? EQUISETOPSIDA Equisetum arvense Field Horsetail G5 S1S2 FILICOPSIDA Adiantum capillus-veneris Southern Maidenhair-fern G5 S2 Asplenium -
Jānis Rukšāns Late Summer/Autumn 2001 Bulb Nursery ROZULA, Cēsu Raj
1 Jānis Rukšāns Late summer/autumn 2001 Bulb Nursery ROZULA, Cēsu raj. LV-4150 LATVIA /fax + 371 - 41-32260 + 371 - 9-418-440 All prices in US dollars for single bulb Dear friends! Again, we are coming to you with a new catalogue and again we are including many new varieties in it, probably not so many as we would like, but our stocks do not increase as fast as the demand for our bulbs. We hope for many more novelties in the next catalogue. Last season we had one more successful expedition – we found and collected 3 juno irises never before cultivated (we hope that they will be a good addition to our Iris collection) and many other nice plants, too. In garden we experienced a very difficult season. The spring came very early – in the first decade of April the temperature unexpectedly rose up to +270 C, everything came up, flowered and finished flowering in few days and then during one day the temperature fell as low as –80 C. A lot of foliage was killed by a returned frost. As a result the crop of bulbs was very poor. The weather till the end of June was very dry – no rain at all, only hot days followed by cold nights. But then it started to rain. There were days with the relative air humidity up to 98%. The drying of harvested bulbs was very difficult. I was forced to clean one of my living rooms in my house, to heat it and to place there the boxes with Allium and Tulipa bulbs to save them from Penicillium. -
Liliaceae Lily Family
Liliaceae lily family While there is much compelling evidence available to divide this polyphyletic family into as many as 25 families, the older classification sensu Cronquist is retained here. Page | 1222 Many are familiar as garden ornamentals and food plants such as onion, garlic, tulip and lily. The flowers are showy and mostly regular, three-merous and with a superior ovary. Key to genera A. Leaves mostly basal. B B. Flowers orange; 8–11cm long. Hemerocallis bb. Flowers not orange, much smaller. C C. Flowers solitary. Erythronium cc. Flowers several to many. D D. Leaves linear, or, absent at flowering time. E E. Flowers in an umbel, terminal, numerous; leaves Allium absent. ee. Flowers in an open cluster, or dense raceme. F F. Leaves with white stripe on midrib; flowers Ornithogalum white, 2–8 on long peduncles. ff. Leaves green; flowers greenish, in dense Triantha racemes on very short peduncles. dd. Leaves oval to elliptic, present at flowering. G G. Flowers in an umbel, 3–6, yellow. Clintonia gg. Flowers in a one-sided raceme, white. Convallaria aa. Leaves mostly cauline. H H. Leaves in one or more whorls. I I. Leaves in numerous whorls; flowers >4cm in diameter. Lilium ii. Leaves in 1–2 whorls; flowers much smaller. J J. Leaves 3 in a single whorl; flowers white or purple. Trillium jj. Leaves in 2 whorls, or 5–9 leaves; flowers yellow, small. Medeola hh. Leaves alternate. K K. Flowers numerous in a terminal inflorescence. L L. Plants delicate, glabrous; leaves 1–2 petiolate. Maianthemum ll. Plant coarse, robust; stems pubescent; leaves many, clasping Veratrum stem.