Handbook of the Iridae (Iridaceae) 1892

Total Page:16

File Type:pdf, Size:1020Kb

Handbook of the Iridae (Iridaceae) 1892 HANDBOOK OF THE IP,IDEAL LONDON WEST NEWMAN AND CO., PRINTERS HATTON GARDEN, E.C. HANDBOOK OF THE IRIDET BY J. G. BAKER, F.R.S., F.L.S., KEEPER OF THE HERBARIUM OF TOE ROYAL GARDENS, KEW. LONDON: GEORGE BELL & SONS, YORK STREET, COVENT GARDEN. AND NEW YORK. 1892. t CONTENTS. ------ ♦------ PAGE P reface ...... V K ey to the G enera .... ix I ris—A ntholyza ..... 1-232 I ndex ....... 283 1 PREFACE. --------♦-------- This is the last of a series of botanical handbooks on which I have been working for a long time. When I first came to Kew, in January, 1866, I found the groups of plants that enter largely into horticulture that most wanted working at were the Vascular Cryptogams and Petaloid Monocotyledons. To those, consequently, during my connection with Kew, I have paid special attention. First, as was agreed upon with Sir Joseph Hooker when I was engaged as first-assistant in the herbarium, I finished the * Synopsis Filicum ’ which Sir William Hooker had planned out and commenced. This was published in 1868, and a second edition, with a Supple­ ment, in 1874. In 1891 I contributed to the fifth volume of the ‘Annals of Botany’ a classified index of the new species discovered up to that date. This has now been issued separately. In the Handbooks of the Fern Allies, Amaryl- lideie, Bromeliaceae, and the present work, I have followed the same concise general plan as in the Fern Synopsis. The Liliacece are dealt with in greater detail in the ‘ Journal of the Linnean Society.’ The papers extend from the eleventh to the eighteenth volume, and cover the whole order, with the exception of the two large genera, Smilax and Allium, which have been monographed recently by M. Alphonse DeCandolle and Dr. Von Ilegel. Those who wish for full bibliographical details about the species of Iridece will find them in a paper V lll PREFACE. entitled “ Systerna Iridacearum ” in the sixteenth volume of the ‘ Journal of the Linnean Society,’ but this contains only descriptions of the genera, not of the species. In the nomenclature and circumscription of the genera I have in the present handbook followed Bentham and Hooker’s ‘ Genera Plantarum,’ with very slight exception. The number of known species of Vascular Cryptogamia now amounts to 3500, and of these orders of Petaloid Monocotyledons to little short of 5000. J. G. BAKER. H erbarium of the R oyal Gardens, K ew, August 17th, 1892. KEY TO THE GENERA. -------- 4-------- Tribe I. Morjea®. — Flowers stalked, usually more than one to a spatlie, often fugitive and opening one after the other. Style- branches placed opposite the stamens and the outer segments of the perianth. * Style-branches furnished with crests that overtop the anthers and transverse stigmas. f Inner segments of the perianth not convolute (temperate regions). 1. I ris.— Perianth usually with a tube above the ovary. Fila­ ments free. Ovary 3-celled. Rootstock usually a rhizome, in § Xiplvion a bulb.— North temperate zone. 2. H ermodactylus. — Like Iris, but ovary 1-celled, with 3 parietal placentas and rootstock digitate.— Mediterranean region. 3. M orjea.— Perianth without a tube. Filaments monadelphous. Ovary 3-celled. Rootstock, except in § Dietes, a tunicated corns.— Cape, Tropical Afnca, Lord Howe's Island. + f Inner segments of the perianth convolute (tropical). 4. Marica. — Perianth without a tube. Style-crests petaloid. Leaves in a distichous rosette, not plicate. Peduncle flattened. Rootstock not bulbous.— Tropical America. 5. Cypella. — Perianth without a tube. Style-crests large, spur-like or flattened. Stems terete. Leaves superposed, plicate. Rootstock bulbous.— Tropical America. G. T r im e z ia . — Perianth without a tube. Style-crests small tubercles or cusps. Stems terete. Leaves not plicate. Rootstock bulbous.— Tropical America. ** Style-branches furnished with terminal stigmas, not overtopping the anthers. 7. T ig r id ia . — Perianth-segments connivent in a cup, then spreading. Style-branches bifid; forks subulate.— Tropical America. 8. H ydrotvenia.— Like Tigridia, but perianth-segments without any spreading blade.— Tropical America. 9 . R ig id e l l a .— Perianth-segments connivent in a cu p ; inner very small; outer with a large reflexed blade. Style-branches bifid ; forks subulate.— Mexico <& Guatemala. 10. H e r bertia.— Perianth-tube none; inner segments small, not convolute. Style-branches bifid at the tip.— Texas <£■ Subtemperate S. Amenca. 1 1 . F erraria. — Perianth-segments subequal, connivent in a cup, joined at the base. Style-branches forked at the tip, densely penicillate.— Cape & Angola. b X KEY TO THE GENERA. 12. H omeria.— Perianth-segments subequal, connivent in a cup at the base, then spreading. Style-branches with two petaloid stigmatose crests.— Cape. 13. H exaglottis.— Perianth-segments subequal, obtuse, spread­ ing from the base. Style-branches cut down to the base into two subulate forks.— Cape. Tribe II. Sisyrinchiee.— Flowers stalked, usually more than one to a spathe, and opening out one after the other, often fugitive. Style-branches alternate with the anthers. Subtribe I. C rocee. — Rootstock a bulb or conn. Spathes essentially 1-flowered. 14. Crocus. — Peduncle short, hidden. Perianth with a long tube and long ascending segments. Style-arms entire or cut into capillary branches.— S. Europe, N. Africa, IF. Asia. 15. S yringodea. — Peduncle short, hidden. Perianth with a long tube; segments spreading or ascending. Style-branches subulate, entire.— Cape. Id. Galaxia.— Peduncle short, hidden. Perianth with a cylin­ drical tube and short obtuse spreading segments. Stigma peltate, petaloid.— Cape. 17. R omulea.— Peduncle produced. Perianth-segments oblong, much exceeding the short tube. Spathe-valves herbaceous.— Mediterranean region, Trop. Africa, Cape. Subtribe II. Cipuree.— Rootstock a bulb or conn. Perianth-tube obsolete. Flowers usually more than one to a spathe, very fugitive.— All American. * Perianth-segments dimorphic. 18. Cipura. — Inner segments connivent. Style-branches dilated. Clusters of flowers sessile, mostly fascicled. Flowers white. 19. Sphenostigma.— Inner perianth-segments spreading. Style- branches dilated. Clusters of flowers peduncled. Flowers generally blue. ** Perianth-segments subequal, obovate-cuneate. 20. E leutherine. — Filaments free. Style-branches long, simple, subulate. Flowers white. 21. Calydorea. — Filaments free. Style-branches subulate, entire or emarginate. Flowers blue or yellow. 22. G elasine. — Filaments united. Style-branches simple, subulate. Flowers blue. 23. Nemastylis. — Filaments free or united. Style-branches cleft to the base into subulate forks. Flowers usually blue. Subtribe III. E usisyrinchiee.— Rootstock not a bulb nor conn. Perianth cleft down to the ovary. Flowers fugitive, usually more than one to a spathe. KEY TO THE GENERA. XI * Perianth-segments unequal. 24. Diplarrhena.— Inner segments shorter, connivent. Upper stamen imperfect.— A ustralia. 25. L ibertia.— Inner segments obovate-cuneate; outer oblong, usually shorter. Stamens all perfect. — Australia, New Zealand, Chili. ** Perianth-segments subequal. 26. Belemcanda.— L eaves broad. Inflorescence a lax corymb. Style-branches flattened and emarginate at the apex. Flowers red, dotted.— China. 27. Orthosanthus. — Clusters panicled. Filaments nearly or quite free. Style-branches subulate. Flowers pale blue, shortly pedicellate.— Australia, Tropical America. 28. B obartia.— Clusters terminal on a leafless peduncle, usually fascicled. Style-branches subulate. Flowers pale yellow, with long pedicels.— Cape. 29. Sisyrinchiuai. — Clusters terminal, single or fascicled. Filaments more or less connate. Style-branches subulate. Flowers usually blue oi yellow ; pedicels long.— America, Sandwich Islands, Ireland. 30. Tapeinia. — Stem very short, bearing a single 1-flowered spathe.— Magellan Straits. Subtribe IY. Ariste.e .— Rootstock not a bulb nor corm. Perianth with a distinct tube above the ovary. Flowers fugitive, usually more than one to a spathe. * Perianth-segments unequal. 31. Patersonia.— Inner segments very small. Filaments con­ nate.— Australia. 32. Cleanthe.— Inner segments the largest, obovate. Filaments free.— Cape. ** Perianth-segments subequal. t Filaments connate. 33. Syjiphyostemon. — Perianth-tube funnel-shaped. Style- branches spreading, subulate.— Chili <£• Southern Andes. 34. ChamjELUM. — Perianth-tube slender. Style shortly tri- cuspidate.— Chili. 35. Solenomelus.— Periantli-tube slender. Style unbranched. — Chili. f t Filaments free. 36. A ristea. — Herbaceous, rarely fruticose. Perianth-tube short, cylindrical. Filaments short, subulate. — Cape, Tropical Africa, Madagascar. 37. W itsen ia.— Fruticose. Perianth-tube funnel-shaped, longer than the segments.— Cape. 38. K lattia. — Fruticose. Perianth-tube short, cylindrical. Filaments very long, filiform.— Cape. X l l KEY TO THE GENERA. Tribe III. Ixie^e.— Flowers spicate,not fugitive,never more than one to a spathe. (This tribe is concentrated at the Cape, but 40, 41, 42, 46, 47, 51, 56, & 57 extend also to the mountains of Tropical Africa, 50 to Socotra, and 56 to the Mediterranean region.) * Style-branches simple. Perianth regular. Stamens equilateral. 39. Schizostylis.— Like Hesperantha, but rootstock not thick­ ened into a conn. 40. H esperantha. — Style short; branches long, subulate. Spatlie-valves green. 41. Geissorhiza. — Style longer than in the last; branches shorter, subulate. Spatlie-valves oblong, green or brownish upwards. 42. D ierama.— Style long, with short clavate branches. Spatlie- valves large,
Recommended publications
  • 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.
    [Show full text]
  • The Taxonomic Status of Gladiolus Illyricus (Iridaceae) in Britain
    The Taxonomic Status of Gladiolus illyricus (Iridaceae) in Britain Aeron Buchanan Supervisor: Fred Rumsey, Natural History Museum, London A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science of Imperial College, London Abstract First noticed officially in Britain in 1855, Gladiolus illyricus (Koch) presents an interesting taxonomic and biogeographical challenge: whether or not this isolated northern population should be recognized as a separate sub-species. Fundamental conservation issues rest on the outcome. Here, the investigation into the relationship of the G. illyricus plants of the New Forest, Hampshire, to Gladiolus species across Europe, northern Africa and the middle east is initiated. Two chloroplast regions, one in trnL–trnF and the other across psbA–trnH have been sequenced for 42 speci- mens of G. illyricus, G. communis, G. italicus, G. atroviolaceus, G. triphyllos and G. anatolicus. Phylogenetic and biogeographical treatments support the notion of an east–west genetic gradation along the Mediterranean. Iberia particularly appears as a zone of high hybridization potential and the source of the New Forest population. Alignment with sequences obtained from GenBank give strong support to the classic taxonomy of Gladiolus being monophyletic in its sub-family, Ixioideae. Comments on these chloroplast regions for barcoding are also given. In conclusion, the genetic localization of Britain’s G. illyricus population as an extremity haplotype suggests that it could well deserve sub-species status. Contents 1 Introduction 2 2 Background 4 3 Materials and Methods 8 4 Results and Discussion 15 5 Conclusions 26 Appendices 28 References 56 1. Introduction G. illyricus in Britain Figure 1: G.
    [Show full text]
  • Weed Risk Assessment for Iris Pseudacorus L. (Iridaceae)
    Weed Risk Assessment for Iris United States pseudacorus L. (Iridaceae) – Yellow Department of flag iris Agriculture Animal and Plant Health Inspection Service September 24, 2013 Version 1 Left: Iris pseudacorus flower. Right: A colony of Iris pseudacorus (source: Bugwood, 2013). Agency Contact: Plant Epidemiology and Risk Analysis Laboratory Center for Plant Health Science and Technology Plant Protection and Quarantine Animal and Plant Health Inspection Service United States Department of Agriculture 1730 Varsity Drive, Suite 300 Raleigh, NC 27606 Weed Risk Assessment for Iris pseudacorus Introduction Plant Protection and Quarantine (PPQ) regulates noxious weeds under the authority of the Plant Protection Act (7 U.S.C. § 7701-7786, 2000) and the Federal Seed Act (7 U.S.C. § 1581-1610, 1939). A noxious weed is defined as “any plant or plant product that can directly or indirectly injure or cause damage to crops (including nursery stock or plant products), livestock, poultry, or other interests of agriculture, irrigation, navigation, the natural resources of the United States, the public health, or the environment” (7 U.S.C. § 7701-7786, 2000). We use weed risk assessment (WRA)— specifically, the PPQ WRA model (Koop et al., 2012)—to evaluate the risk potential of plants, including those newly detected in the United States, those proposed for import, and those emerging as weeds elsewhere in the world. Because the PPQ WRA model is geographically and climatically neutral, it can be used to evaluate the baseline invasive/weed potential of any plant species for the entire United States or for any area within it. As part of this analysis, we use a stochastic simulation to evaluate how much the uncertainty associated with the analysis affects the model outcomes.
    [Show full text]
  • For the Flora of Central Asia
    ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at KHASSANOV & RAKHIMOVA • The genus Iris in Central Asia STAPFIA 97 (2012): 174–179 Taxonomic revision of the genus Iris L. (Iridaceae Juss.) for the flora of Central Asia F. O. KHASSANOV* & N. RAKHIMOVA Abstract: A new conspectus of the genus Iris (including the genera Juno and Iridodictyum) is presented for the rich flora of Central Asia. Two new combinations as well as new epithetha for two species are proposed. Zusammenfassung: Die Gattung Iris (inklusive der Gattungen Juno und Iridodictyum) wurde für die reiche Flora Zentralasiens systematisch bearbeitet. Zwei neue Kombinationen, sowie neue Epitheta für zwei Arten werden vorgeschlagen. Key words: Taxonomy, Iris, Juno, Central Asia, nomenclature. * Correspondence to: [email protected] Introduction ulate bulb tunics. Amazingly that 36 species of Iris are endemic for this area (fig. 1–3). Nomenclature changes has been started by P. WENDELBO (1975). R. KAMELIN (1981) and later on T. Hall During the last 70 years in all floristic revisions for Central et A. SEISUMS (2011) made several new combinations from Juno Asia made by A. I. VVEDENSKY (1941, 1971) section Juno was restoring to Iris. Nevertheless, several taxa needed in nomen- treated as a separated genus. 30 species were mentioned and sev- clature correction as well new ones described recently from this eral new species were newly described in his last revision. In- area. No doubt, that Central Asia can be treated as one of the terestingly enough, that all other genera of Iridaceae (including largest centers of biodiversity of genus Iris L. and proposed con- Iris) has been revised in “Conspectus Florae Asiae Mediae” by spectus given below based on revisions of R.
    [Show full text]
  • Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property
    Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property. Los Alerces National Park, Argentina 185 Map 2: Andean-North Patagonian Biosphere Reserve: Context for the Nominated Proprty. Los Alerces National Park, Argentina 186 Map 3: Vegetation of the Valdivian Ecoregion 187 Map 4: Vegetation Communities in Los Alerces National Park 188 Map 5: Strict Nature and Wildlife Reserve 189 Map 6: Usage Zoning, Los Alerces National Park 190 Map 7: Human Settlements and Infrastructure 191 Appendix 2: Species Lists Ap9n192 Appendix 2.1 List of Plant Species Recorded at PNLA 193 Appendix 2.2: List of Animal Species: Mammals 212 Appendix 2.3: List of Animal Species: Birds 214 Appendix 2.4: List of Animal Species: Reptiles 219 Appendix 2.5: List of Animal Species: Amphibians 220 Appendix 2.6: List of Animal Species: Fish 221 Appendix 2.7: List of Animal Species and Threat Status 222 Appendix 3: Law No. 19,292 Append228 Appendix 4: PNLA Management Plan Approval and Contents Appendi242 Appendix 5: Participative Process for Writing the Nomination Form Appendi252 Synthesis 252 Management Plan UpdateWorkshop 253 Annex A: Interview Guide 256 Annex B: Meetings and Interviews Held 257 Annex C: Self-Administered Survey 261 Annex D: ExternalWorkshop Participants 262 Annex E: Promotional Leaflet 264 Annex F: Interview Results Summary 267 Annex G: Survey Results Summary 272 Annex H: Esquel Declaration of Interest 274 Annex I: Trevelin Declaration of Interest 276 Annex J: Chubut Tourism Secretariat Declaration of Interest 278
    [Show full text]
  • Native Plant Diversity and Composition Across a Pinus Radiata D.Don Plantation Landscape in South-Central Chile—The Impact Of
    Article Native Plant Diversity and Composition Across a Pinus radiata D.Don Plantation Landscape in South-Central Chile—The Impact of Plantation Age, Logging Roads and Alien Species Steffi Heinrichs 1,*, Aníbal Pauchard 2,3 and Peter Schall 1 1 Department Silviculture and Forest Ecology of the Temperate Zones, University of Goettingen, 37077 Göttingen, Germany; [email protected] 2 Facultad de Ciencias Forestales, Universidad de Concepción, Concepción 3349001, Chile; [email protected] 3 Institute of Ecology and Biodiversity (IEB), Santiago 8320000, Chile * Correspondence: [email protected]; Tel.: +49-551-395-974 Received: 18 July 2018; Accepted: 12 September 2018; Published: 14 September 2018 Abstract: Alien tree plantations are expanding globally with potential negative effects for native biodiversity. We investigated plant species diversity and composition in a Pinus radiata landscape in south-central Chile, a biodiversity hotspot, by sampling understory vegetation in different plantation age classes, along forest roads and in natural forest remnants in order to find effective conservation measures for native biodiversity. Plantations, including different age classes and roadsides, maintained high native species richness at the landscape scale but supported a completely different community composition than natural forests. Thus, natural forest remnants must be conserved as plantations cannot replace them. Certain natural forest species occurred frequently in mature plantations and can represent starting points for retaining natural elements in plantations. Generalist native and alien species benefited from plantation management, mainly in young plantations and along roadsides. Stand maturation and a closed canopy, though, reduced alien species occurrences within plantations. Along roads, shade-tolerant aliens should be monitored and removed as they can potentially invade natural forests.
    [Show full text]
  • Iridaceae – Iris Family
    IRIDACEAE – IRIS FAMILY Plant: herbs, perennial; can be shrub-like elsewhere Stem: Root: growing from rhizomes, bulbs, or corms Leaves: simple, alternate or mostly basal (sheaths open or closed), most grass or sword-like with parallel veins Flowers: perfect, regular (actinomorphic) or irregular (zygomorphic); flowers showy, often solitary; flowers in 3’s (petals, sepals, and stamens), both sepals and petals often colored; regular as in Blue-Eyed grasses (looks like 6-plan), or irregular as in true Irises; flower subtended by 2 bracts; ovary mostly inferior, 3 carpels, 1 style Fruit: capsule with seed Other: Monocotyledons Group Genera: 65+ genera; locally Belamcanda (blackberry-lily), Iris (iris), Sisyrinchium (blue-eyed grass) WARNING – family descriptions are only a layman’s guide and should not be used as definitive Flower Morphology in the Iridaceae (Iris Family) Examples of some common genera German Iris [Blue Flag] Iris germanica L. (Introduced Blackberry Lily Belamcanda chinensis (L.) DC. (Introduced) Dwarf Crested Iris Stout Blue-Eyed Grass Iris cristata Aiton Sisyrinchium angustifolium Mill. Copper [Red] Iris Iris fulva Ker Gawl. Prairie Blue-Eyed Grass Sisyrinchium campestre E.P. Bicknell IRIDACEAE – IRIS FAMILY Blackberry Lily; Belamcanda chinensis (L.) DC. (Introduced) Dwarf Crested Iris; Iris cristata Aiton Copper [Red] Iris; Iris fulva Ker Gawl. German Iris [Blue Flag]; Iris germanica L. (Introduced) Yellow Iris [Flag]; Iris pseudacorus L. (Introduced) Southern Blue Flag [Shreve's Iris]; Iris virginica L. var. shrevei (Small) E.S. Anderson Common Blue-Eyed Grass; Sisyrinchium albidum Raf. Stout Blue-Eyed Grass; Sisyrinchium angustifolium Mill. Eastern Blue-Eyed Grass; Sisyrinchium atlanticum E.P. Bicknell Prairie Blue-Eyed Grass; Sisyrinchium campestre E.P.
    [Show full text]
  • Wild Watsonia (DPI Vic)
    May 2000 Wild watsonia LC0251 Keith Turnbull Research Institute, Frankston ISSN 1329-833X This Landcare Note describes the weed Wild watsonia, West Gippsland, the central highlands and the Geelong Watsonia meriana var. bulbillifera, and related species region. and outlines options for its management. Description Common Name An erect perennial herb forming large clumps; similar to Wild watsonia, bulbil watsonia gladiolus, with strap-like leaves, slender reddish flowering stems 0.5 to 2 m high, pink, orange or red flowers, Botanical Name underground corms and clusters of small corms (known as Watsonia meriana (L.) Miller var. bulbillifera (J.W. bulbils or cormils) on the stems. Leaves and flowering Matthews & L. Bolus) D.A. Cooke heads are produced annually. Family Iridaceae (Iris family) Status Under the Catchment and Land Protection Act, wild watsonia is a Regionally Controlled Weed in the Glenelg, Corangamite, Port Phillip West, Port Phillip East, North East, East Gippsland and West Gippsland Regions. Land owners in areas where wild watsonia is Regionally Controlled must take all reasonable steps to control it and prevent its spread on their land and the roadsides which adjoin their land. Wild watsonia is mainly a weed of roadsides, railway reserves, the edges of water courses, open woodland, unimproved pastures and neglected areas. Origin and Distribution Native to South Africa, wild watsonia was originally introduced to Australia as a garden ornamental. It was considered naturalised in Victoria by 1907 and was spread widely in the 1940s as a fashionable garden plant. It is also a weed in New Zealand and on the Indian Ocean islands of Mauritius and Reunion.
    [Show full text]
  • Sisyrinchium Sarmentosum Suksd
    Sisyrinchium sarmentosum Suksd. ex Greene pale blue-eyed grass Iridaceae - iris family status: State Threatened, Federal Species of Concern, BLM sensitive, USFS sensitive rank: G2 / S1S2 General Description: A dapted from Flora of North A merica (1993+): Tufted perennial herb up to 32 cm tall. Stems unbranched, 1.7-2.8 mm wide, hairless, compressed, 2-winged; margins entire and similar to stem body. Leaves hairless, narrow, elongate but generally shorter than the stem, overlapping and sheathing at the base. Floral Characteristics: Inflorescence solitary and terminal; flowers 2-7 on slender pedicels. Sheathing bracts 2, green, hairless, keels smooth. O uter bract 27-48 mm, 14-17 mm longer than the inner bract, margins basally fused for 3-5 mm. Inner bracts with translucent margins up to 0.5 mm wide. Tepals 6, pale blue with yellow bases; outer tepals 10-14 mm, with tips rounded and awned. Filaments fused; anthers yellow. Fruits: Tan to medium brown capsules, globe-shaped, 4-5 mm. Seeds 1-1.5 mm, minutely wrinkled. Flowers and fruits mid-June to mid-A ugust. Identif ication Tips: This species is not in Hitchcock & Cronquist (1973), but would mistakenly key to S. angus tifolium, whic h grows only in the eastern U.S. S. s eptentrionale is the only other member of the genus with pale blue tepals in our area; it has shorter outer tepals (8-9.1 mm), and outer bracts 17-42 mm longer than the inner bract. The length/width ratio of the outer tepals is 2.6-3.0 for S.
    [Show full text]
  • Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes
    Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Shichao Chen1., Dong-Kap Kim2., Mark W. Chase3, Joo-Hwan Kim4* 1 College of Life Science and Technology, Tongji University, Shanghai, China, 2 Division of Forest Resource Conservation, Korea National Arboretum, Pocheon, Gyeonggi- do, Korea, 3 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, United Kingdom, 4 Department of Life Science, Gachon University, Seongnam, Gyeonggi-do, Korea Abstract Phylogenetic analysis aims to produce a bifurcating tree, which disregards conflicting signals and displays only those that are present in a large proportion of the data. However, any character (or tree) conflict in a dataset allows the exploration of support for various evolutionary hypotheses. Although data-display network approaches exist, biologists cannot easily and routinely use them to compute rooted phylogenetic networks on real datasets containing hundreds of taxa. Here, we constructed an original neighbour-net for a large dataset of Asparagales to highlight the aspects of the resulting network that will be important for interpreting phylogeny. The analyses were largely conducted with new data collected for the same loci as in previous studies, but from different species accessions and greater sampling in many cases than in published analyses. The network tree summarised the majority data pattern in the characters of plastid sequences before tree building, which largely confirmed the currently recognised phylogenetic relationships. Most conflicting signals are at the base of each group along the Asparagales backbone, which helps us to establish the expectancy and advance our understanding of some difficult taxa relationships and their phylogeny.
    [Show full text]
  • Sisyrinchium Hastile Bickn
    Sisyrinchium hastile Bickn. blue-eyed-grassblue-eyed-grass, Page 1 State Distribution No photo available Best Survey Period Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Status: State extirpated Total range: The sole collection of this blue-eyed- grass was made on Belle Isle in the Detroit River in Global and state rank: GHQ/SX Wayne County. Other common names: spear-like blue-eyed-grass. Recognition: Plants of S. hastile are dull green, erect, and quite slender, ranging from 30-40 cm in Family: Iridaceae (Iris family) height and “apparently little if at all tufted” (Bicknell 1899). The stems are slightly roundish to at best Taxonomy: Similar to Sisyrinchium farwellii Bickn., somewhat compressed, but not strongly flattened this species is known only from the type collection, and 2-winged. Flowers are borne in a loose cluster made in Michigan by O. A. Farwell in 1896, and is of terminating the simple stem, arising from an erect, leaf- questionable origin and distinction. Farwell noted on like (involucral) bract and a series of smaller one collection sheet that the plant was “very rare” and bracts (the 2 spathes) that are stalkless. The inner “perhaps only a stray immigrant”. Bicknell (1899) spathe (which like the outer consists of a pair of bracts) considered it to be a very distinct plant not closely has 2-3 cm long bracts. S. albidum, a relatively related to other Michigan species. Britton and Brown common species of southern Lower Michigan, usually (1913) suggested that this species closely resembles the has shorter inner spathe bracts and anthers 2.5 mm long Mexican S.
    [Show full text]
  • Seasonality, Growth, and Net Productivity of Herbs and Shrubs Of
    Abstract: The physiognomy and species composition Seasonality, Growth, and Net Productivity of of the matorral, as well as growth period and net Herbs and Shrubs of the Chilean Matorral1 productivity of shrubs, change with altitude. In shrubs, vegetative growth period is shorter at higher altitudes; leaf area indices are signifi- cantly higher at lower sites, while biomass Gloria Montenegro, María E. Aljaro, Alan Walkowiak, and indices increase with altitude. At the community 2 Ricardo Saenger level, productivity is lower in the montane matorral. Growth and productivity of the herba- ceous understory markedly varies depending on precipitation. Most vegetative growth occurs between winter and early spring. Chile, located between 18° and 56° latitude The midelevation matorral in the Coastal Range south, has a climate which markedly varies accord- and the sclerophyllous scrub at the foothills of ing to geographical position (Di Castri 1968, the Andes are replaced at about 1850 m by a mon- Hajek and Di Castri 1975). Drought predominates tane evergreen scrub community (Mooney and others in the north of the country and rainfall is char- 1970, Rundel and Weisser 1975, Hoffmann and acteristic of the central and southern regions. Hoffmann 1978, Montenegro and others 1979b). At The natural vegetation is closely related to the 2300 m in the Andes the matorral gives way to a different climatic patterns. The northern part of low subalpine scrub. Over 3000 m, alpine herbs the country is desertic, while evergreens predomi- and cushion plants predominate (Villagran and nate in the south (Pisano 1954, Di Castri 1968, others 1979, Arroyo and others 1979).
    [Show full text]