C3 Primitive Angiosperms

Total Page:16

File Type:pdf, Size:1020Kb

C3 Primitive Angiosperms Magnoliids & other Primitive Angiosperms Revised 5th of May 2015 Angiosperm, pl angiosperms; Angiospermae n (Greek anggeion (angeion), vessel, small container, & Greek σπέρµα, sperma, seed) A major division of the plant kingdom, commonly called flowering plants as their reproductive organs are in flowers, having seeds which develop in a closed ovary made of carpels, a very reduced gametophyte, & endosperm develop from a triple fusion nucleus; flowering plant producing seeds enclosed in a structure derived from the ovary; flowering plant, plants with ovules enclosed in ovary. A division of the seed plants (spermatophytes) that bear ovules & seeds in closed megaspores (carpels) in contrast to gymnosperms, which have exposed ovules & seeds, born “naked” on the megasporophylls. Angiosperms are distinguished by a unique process of sexual reproduction called “double fertilization”. According to the number of leaves (cotyledons) present in the embryo, two major groups are distinguished, the Monocotyledons & the Dicotyledons. Angiosperms are commonly referred to as “flowering plants: even though the reproductive organs of some gymnosperms are also borne in structures that fulfill the definition of a flower. Cf gymnosperm. Angiosperms have traditionally been split into monocotyledons & dicotyledons, or plants with one or two seed leaves respectively. One group of plants that have two seeds leaves was problematic, as it also had primitive flowers & some traits in common with monocots. This group is the Magnoliids, or primitive angiosperms. The remainder of the dicots are called Eudicots, the prefix eu-, from Greek ἐὐς, eus, good, meaning the good dicots. Magnoliids (Eumagnoliids?) About 8,500 (5,000-9,000) spp in 20 angiosperm families, of large trees, shrubs, vines, lianas, & herbs that are neither eudicotyledons nor monocotyledons, distributed in tropical & temperate areas. They are also referred to as primitive angiosperms, the primitiveness demonstrated by flowers that have fewer or less differentiated parts. Most spp have long, broad, net-veined leaves & large flowers, 3-merous, with numerous, spirally arranged tepals (perianth parts that are not differentiated into petals & sepals), stamens, & carpels, & pollen with a single pore (like the monocotyledons). Most have fused carpels, some also have leaf-like stamens & vesselless wood. Many have cells with ether-containing oils. The seeds have embryos with two cotyledons (like the eudicotyledons). The group is polyphyletic, or not sharing a common ancestor. They are sometimes split into woody magnoliids & paleoherbs. Woody magnoliids have large, often showy, bisexual flowers. Paleoherbs have small flowers with few parts, & they may be unisexual. Magnoliids include many spp of economic importance, including avocados (Persea americana), guanabana, sour sop, cherimoya, & sweet sop (Annona spp), black & white pepper (Piper nigrum), bay leaves (Laurus nigrus), nutmeg (Myristica fragrans), cinnamon (Cinnamomum verum), camphor (Cinnamomum camphora), ornamentals (Magnolia) & lumber (Liriodendron). Other spp are known for narcotic, hallucinogenic, & paralytic properties. The hallucinogenic compound myristicin comes from the spice NUTMEG. The Magnoliids include most, but not all, WATER LILIES. Like other intricate plants, WATER LILY nomenclature is the stuff of bad dreams. The families include the following: ANNONACEAE AL de Jussieu 1789 CUSTARD-APPLE FAMILY, ARISTOLOCHIACEAE AL de Jussieu 1789 BIRTHWORT FAMILY, CABOMBACEAE A Richard 1828 WATER-SHIELD FAMILY, CALYCANTHACEAE Lindley 1819 SWEET-SHRUB FAMILY, ILLICIACEAE AC Smith 1947 STAR-ANISE FAMILY, LAURACEAE AL de Jussieu 1789 LAUREL FAMILY, MAGNOLIACEAE AL de Jussieu 1789 MAGNOLIA FAMILY, NYMPHAEACEAE RA Salisbury 1805 WATER-LILY FAMILY, PIPERACEAE CA Agardh 1824 PEPPER FAMILY, SCHISANDRACEAE Blume 1830 STAR-VINE FAMILY, & SAURURACEAE E Meyer 1827 LIZARD'S-TAIL FAMILY, TABLE OF CONTENTS PRIMITIVE ANGIOSPERMS BACK TO TOP ANNONACEAE Asimina NYMPHAEACEAE Brasenia ARISTOLOCHIACEAE Asarum Castalia CABOMACEAE Brasenia Nelumbo LAURACEAE Lindera Nuphar Sassafras Nymphaea MAGNOLIACEAE Liriodendron SAURURACEAE Saururus Magnolia ANNONACEAE AL de Jussieu 1789 Custard-apple Family, Anonads A family of about 128 genera & about 2300 spp of trees, shrubs, & lianas, primarily tropical. Anonaceae in some older sources. The wood of Annona glabra fluoresces dull yellow under ultraviolet lights. ASIMINA Adanson 1763 Pawpaw Annonaceae Asimina (Assimina), Asiminum (a-SI-mi-na or asim’ina) The name for Asimina triloba, New Latin, from the North American Indian name assimin, or from the French- Indian name assiminier, from American French assimine papaw, modification of Illinois rassimina, from rassi divided lengthwise into equal parts & mina seeds. One source gives American Indian assimin through French asiminier, or a French-Canadian name asiminier, used by Adanson*. Eastern North American endemic genus of 8 spp of deciduous shrubs & small trees having aromatic alternate leaves & flowers with 3 to 15 stamens & carpels. Former genus names include Uvaria & Porcelia. The tropical papaya is Carica paypaya. Several spp of Asimina are larval hosts for the Zebra Swallowtail Butterfly. *Michel Adanson’s, a French botanist of Scottish descent, naming style gave rise to the term an ‘Adansonian name’, or a name that has an unknown basis or little basis relative to the plant described. Asimina spp. Photos & line drawing courtesy of the US Forest Service USDA-NRCS PLANTS Database. Asimina triloba (Linnaeus) Dunal *NJ, NY COMMON PAW-PAW, aka ASIMINA, ACIMINIER, BANANA TREE, BANANGO, CUSTARD APPLE, DOG BANANA, DOG-BANANA, FALSE BANANA, FETID-SHRUB, HOOSIER BANANA, INDIAN-BANANA, INDIANA BANANA, KANSAS BANANA, KENTUCKY BANANA, MICHIGAN BANANA, MISSOURI BANANA, OZARK BANANA, PAPAU, PAPAW, PAW PAW, PAWPAW, PAWPAW APPLE, PAWPAWTREE, POSSUMHAW, PRAIRIE BANANA, POOR MAN'S BANANA, WEST VIRGINIA BANANA, (trilobus -a -um (tri-LO- bus) with three lobes, from Latin tri, prefix from tres, three, & Late Latin lobus, husk, pod noun from Greek λοβος, lobos, lobe of the ear, liver, or lung, also a capsule or pod of a legume, in reference to the calyx, the outer most flower whorl) The common name probably came from the Arawakan name of papaya (or alternately from Spanish papaya), for the similarity of the fruits. Habitat: Rich woods & alluvium, woods & thickets, wooded slopes, alluvial soils. Deciduous forests, on slopes of ravines, along streams, & floodplains. In the se USA, “Alluvial forests, other moist, nutrient-rich forests” (w12). In Michigan, deciduous forests, swamps, thickets along streams (rvw11). distribution/range: Native from western New York & southwest Ontario to Iowa, south to Florida & east Texas. Its northern range may have been extended by Native Americans. In most Illinois cos except in the northern tier & northwest. It is rumored to grow in some sheltered coves in the upper reaches of Bureau Creek. Culture: Propagation: By seed or bud graft. Fruit set is very low, 0.45%, compared to the number of flowers. Seeds usually 2-3 large, dark brown; remove from pulpy matrix. Delayed germination is caused by slowly permeable seedcoats & dormant embryos; seed from a southern source germinated 100% without cold treatment; three seed lots given 60 day cold stratification germinated 50, 62, & 82%; fall sowing untreated seed did not improve germination; dormant seeded seeds may germinate over a two year period; seedlings have a long taproot. Fruits ripen late summer to fall. Collect fruits when they turn from green to yellow green and the seed coats are light brown. The fruits can be ripened indoors in a paper bag, but the overripe fruit develop an unpleasant odor. Seeds have a pulpy skin that can be removed by soaking in a bucket of water for a week. Code B seeds will germinate upon shifting to 70ºF after 90 days of cold moist stratification at 40ºF, and G chemical inhibitors, & * seeds are hydrophilic, intolerant of dry storage. Outdoor-planted seeds are subject to small mammal granivory, best stratified in ziplock in a refrigerator. Cultivars are grafted onto seeding stock. Propagation from sed is the preferred method. (cu02) Seed must have 90-120 days cold moist stratification in moist sphagnum at 34-40ºF, overwinter filed planted seed. Germination is hypogeal, shoots emerge without cotyledons. Green house germination occurs in about 7 weeks, field planted seeds in following July or August. 10” taproot develops before shoots emerge. (crfg) “Fruit often drops from tree while still hard, green & sour. These fruits can be stored in single layers on trays until pulp begins to soften. Remove seeds & air dry before storing. Trees are easily grown from scarified/stratified seed. Follow scarification with a 60-90 day stratification at 41 degrees. Fall sow in a shady location. Some sources say seed is the only method of propagation while other say increase is possible by root cuttings or layering.” (lbj) Can be grown from seed sown in fall in a cold frame or in pots of sandy soil in a heated greenhouse in winter, as well as by layering or root cuttings; best in well-drained, loamy soil in a sunny sheltered location; not easy to transplant. Medium growth rate. Kew Royal Botanic Garden notes Storage Behaviour: Uncertain; Thousand Seed Weight: 810g; Dispersal: Animal; Oil content: 38.0%. Cultivation: Hard to transplant, due to fleshy, brittle roots with few fine root hairs. Transplant from container grown seedlings after bud break. Provide good drainage & keep well watered. Prefers moist,
Recommended publications
  • ABSTRACT CULATTA, KATHERINE EMILY. Taxonomy, Genetic
    ABSTRACT CULATTA, KATHERINE EMILY. Taxonomy, Genetic Diversity, and Status Assessment of Nuphar sagittifolia (Nymphaeaceae). (Under the direction of Dr. Alexander Krings and Dr. Ross Whetten). Nuphar sagittifolia (Walter) Pursh (Nymphaeaceae), Cape Fear spatterdock, is an aquatic macrophyte considered endemic to the Atlantic Coastal Plain and of conservation concern in North Carolina, South Carolina, and Virginia. The existence of populations of unclear taxonomic identity has precluded assessment of the number of populations, distribution, and conservation needs of N. sagittifolia. Thus, the first objective of this thesis was to re-assess the circumscription of the species by evaluating four taxonomic hypotheses: 1) Populations of Nuphar in the N. sagittifolia range, including morphological intermediates, are members of a single polymorphic species; 2) Morphological intermediates in the N. sagittifolia range are hybrids between N. advena subsp. advena and N. sagittifolia; 3) Morphological intermediates are variants of N. advena subsp. advena or N. sagittifolia; 4) Intermediates, distinct from both N. advena subsp. advena and N. sagittifolia, are either disjunct populations of N. advena subsp. ulvacea or members of an undescribed taxon. The second objective was to summarize information on the taxonomy, biology, distribution, and genetic diversity of N. sagittifolia s.s to inform conservation decisions. Approximately 30 individuals from each of 21 populations of Nuphar across the N. sagittifolia range, and the type populations of N. advena subsp. advena, N. advena subsp. ulvacea, and N. sagittifolia were included in genetic and morphological analyses. Individuals were genotyped across 26 SNP loci identified for this study, and 31 leaf, flower and fruit morphological characters were measured. STRUCTURE analysis identified three genetic groups with corresponding morphological differences in the N.
    [Show full text]
  • The Potential Use of Annona (Annonaceae) by Products As a Source of Botanical Insecticides
    The potential use of Annona (Annonaceae) by products as a source of botanical insecticides Leandro do Prado Ribeiroa*, Camila Moreira de Souzab, Keylla Utherdyany Bicalhoc, Edson Luiz Lopes Baldinb, Moacir Rossi Forimc, João Batista Fernandesc, José Djair Vendramimd a Research Center for Family Agriculture, Agricultural Research and Rural Extension Company of Santa Catarina (CEPAF/EPAGRI), Chapecó, Santa Catarina, Brazil. *E-mail: [email protected]; bDepartment of Crop Protection, College of Agricultural Sciences, São Paulo State University (FCA/UNESP) Botucatu, São Paulo, Brazil; d Department of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, São Paulo, Brazil; c Department of Entomology and Acarology, “Luiz de Queiroz” College of Agriculture, University of São Paulo (ESALQ/USP), Piracicaba, São Paulo, Brazil. INTRODUCTION In addition, some species of Annona genera (e.g.: Annona muricata, Annona squamosa, Annona cherimolia, and Annona The structural and functional diversity of secondary metabolites cherimolia x Annona squamosa) have great economic (allelochemicals) is a key factor for the survival and evolutionary importance due to their edible fruits of ample commercial success of plant species inhabiting an environment with an interest. Consequently, a considerably cultivated area (~ 14,000 abundance of natural enemies. Therefore, the tropical flora, hectares) with these species is observed in Brazil. However, most with its unique biodiversity, is a promising natural reservoir of of Annona fruits production are destined for fruit-processing bioactive substances. In this context, Brazil has the highest plant industries and commercialized as frozen pulps for juice genetic diversity in the world offering enormous potential for preparations due to its small shelf life.
    [Show full text]
  • Introduction to Common Native & Invasive Freshwater Plants in Alaska
    Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting
    [Show full text]
  • In Planta Expression of Exocellulase Enzymes for Bio-Ethanol Production
    In planta expression of exocellulase enzymes for Bio-ethanol production A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Parsu Ram Budathoki Degree of Bachelor of Science, University of North Bengal, India Master of Science in Biotechnology, Bangalore University, India School of Science College of Science, Engineering and Health RMIT University March 2018 Declaration I certify that except where due acknowledgement has been made, the work is that of the author alone; the work has not been submitted previously, in whole or in part, to qualify for any other academic award; the content of the thesis is the result of work which has been carried out since the official commencement date of the approved research program; any editorial work, paid or unpaid, carried out by a third party is acknowledged; and, ethics procedures and guidelines have been followed. Parsu Ram Budathoki Date: 13/03/2018 i ACKNOWLEDGEMENTS I wish to thank my senior supervisor, Professor Trevor Stevenson for his help and advice during the period of research. I also thank my secondary supervisor Dr Gregory Nugent for his guidance and assistance. I thank Professor David Stalker for many useful discussions. I am indebted to Mrs. Kim Stevenson for her assistance and guidance in my laboratory work. I also thank Dr. Chung Hong Chen (former CSIRO Scientist) for providing me with plasmids and helping me in the cloning vectors. I acknowledge Dr. Chaitali Dekiwadia for assistance in sample preparation and imaging of TEM work at RMIT Microscopy and Microanalysis Facility. The research described in this thesis was carried on while I held a research scholarship from the ARC Linkage grant in partnership with Biomass Conversion Technologies, was funded from Chevron Technology Ventures in USA is gratefully acknowledged.
    [Show full text]
  • Ceylon Cinnamon • Pure Cinnamon • Mexican Cinnamon • Sri Lanka Cinnamon • Canela (Spanish for Cinnamon)
    Cinnamon The 4th most valuable spice in the world http://www.trueceylonspices.com/ceylon-cinnamon/ www.truecylonspices.com 1. About Cinnamon is a first traded and most popular spice from the ancient time. It extracts from the bark of the cinnamon tree have also been used traditionally as medicine throughout the world. www.truecylonspices.com 2. Products of Cinnamon • Cinnamon Quills (Full tubes) • Cinnamon Quillings (broken tubes) • Cinnamon Featherings • Cinnamon Chips • Ground Cinnamon (Cinnamon powder) • Cinnamon Leaf Oil • Cinnamon Bark Oil www.truecylonspices.com 3. Varieties 1. Cassia Cinnamon 1. Cinnamomum loureiroi 2. Cinnamomum aromaticum 3. Cinnamomum burmannii 2. True Cinnamon 1. Cinnamomum verum www.truecylonspices.com 3.1.1 Cinnamomum loureiroi • Other names: • Saigon Cinnamon • Vietnamese cinnamon • Vietnamese cassia • Origin: • Vietnam • Pros: • Strong spicy cinnamon taste • high levels of oil content Image credit: Wikipedia • Cons: • High Coumarin Levels www.truecylonspices.com 3.1.2 Cinnamomum aromaticum • Other names: • Cinnamomum cassia (old Latin name) • Cassia • Chinese cinnamon • Chinese cassia • Tung Hing • Origin: • China • Pros: • Cheap Image credit: Wikipedia • Cons: • High Coumarin Levels www.truecylonspices.com 3.1.3 Cinnamomum burmannii • Other names: • Korintje cassia • Padang cassia • Batavia cassia • Indonesian cinnamon • Origin: • Indonesia • Pros: • Cheap • Spicy Cinnamon flavor Image credit: Wikipedia • Cons: • High Coumarin Levels www.truecylonspices.com 3.2.1 b. Cinnamomum verum • Other names: • Cinnamomum zeylanicum (old Latin name) • True Cinnamon • Ceylon Cinnamon • Pure cinnamon • Mexican cinnamon • Sri Lanka cinnamon • Canela (Spanish for cinnamon) • Origin: • Sri Lanka (90%), • India, Madagascar, Brazil, Caribbean • Pros: • Ultra Low Coumarin levels • Softer and subtle taste • crumbly • Cons: • Expensive www.truecylonspices.com 4. Usage of Cinnamon • Usage of Cinnamon bark • As a spice.
    [Show full text]
  • Aquatic Vascular Plant Species Distribution Maps
    Appendix 11.5.1: Aquatic Vascular Plant Species Distribution Maps These distribution maps are for 116 aquatic vascular macrophyte species (Table 1). Aquatic designation follows habitat descriptions in Haines and Vining (1998), and includes submergent, floating and some emergent species. See Appendix 11.4 for list of species. Also included in Appendix 11.4 is the number of HUC-10 watersheds from which each taxon has been recorded, and the county-level distributions. Data are from nine sources, as compiled in the MABP database (plus a few additional records derived from ancilliary information contained in reports from two fisheries surveys in the Upper St. John basin organized by The Nature Conservancy). With the exception of the University of Maine herbarium records, most locations represent point samples (coordinates were provided in data sources or derived by MABP from site descriptions in data sources). The herbarium data are identified only to township. In the species distribution maps, town-level records are indicated by center-points (centroids). Figure 1 on this page shows as polygons the towns where taxon records are identified only at the town level. Data Sources: MABP ID MABP DataSet Name Provider 7 Rare taxa from MNAP lake plant surveys D. Cameron, MNAP 8 Lake plant surveys D. Cameron, MNAP 35 Acadia National Park plant survey C. Greene et al. 63 Lake plant surveys A. Dieffenbacher-Krall 71 Natural Heritage Database (rare plants) MNAP 91 University of Maine herbarium database C. Campbell 183 Natural Heritage Database (delisted species) MNAP 194 Rapid bioassessment surveys D. Cameron, MNAP 207 Invasive aquatic plant records MDEP Maps are in alphabetical order by species name.
    [Show full text]
  • Redalyc.Antioxidant Capacity and Total Phenol Content of Hyptis Spp., P
    Revista Colombiana de Química ISSN: 0120-2804 [email protected] Universidad Nacional de Colombia Colombia Tafurt-García, Geovanna; Jiménez-Vidal, Luisa F.; Calvo-Salamanca, Ana M. Antioxidant capacity and total phenol content of Hyptis spp., P. heptaphyllum, T. panamensis, T. rhoifolia and Ocotea sp. Revista Colombiana de Química, vol. 44, núm. 2, 2015, pp. 28-33 Universidad Nacional de Colombia Bogotá, Colombia Available in: http://www.redalyc.org/articulo.oa?id=309044127005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Geovanna Tafurt-García1,*, Luisa F. Jiménez-Vidal1, Ana M. Calvo-Salamanca1 1.Orinoquía´s Science Research Group, Universidad Nacional de Colombia, sede Orinoquia, km 9, to Caño Limón, Arauca, Colombia. *Corresponding author: [email protected]. Recibido: 19 de junio de 2015 Aceptado: 10 de julio de 2015 Antioxidant capacity Capacidad antioxidante Capacidade antioxidante and total phenol y contenido de fenoles e conteúdo de fenóis content of Hyptis spp., totales de Hyptis spp., totais de Hyptis spp., P. heptaphyllum, T. P. Heptaphyllum, T. P. Heptaphyllum, T. panamensis, T. rhoifolia Panamensis, T. Rhoifolia, y Panamensis, T. Rhoifolia, e and Ocotea sp. Ocotea sp. Ocotea sp. Química Aplicada y Analítica Abstract Resumen Resumo In this work, the possible correlation En este trabajo se evaluó la posible Neste trabalho foi avaliada a possível between the antioxidant activities and correlación entre las actividades correlação entre as atividades antioxidantes, the Total Phenolic Content (TPC) and antioxidantes, el contenido de fenoles o conteúdo de fenóis totais e a composição chemical composition of Lamiaceae (H.
    [Show full text]
  • Proefschrift RHJ Erkens V2.Qxp
    REFERENCES Aldrich, J., Cherney, B. W., Merlin, E. & Christopherson, L. 1988. The role of insertions/deletions in the evolution of the intergenic region between psbA and trnH in the chloroplast genome. Cur. Genet. 14: 137-147. Alfaro, M. E., Zoller, S. & Lutzoni, F. 2003. Bayes or Bootstrap? A simulation study comparing the performance of Bayesian Markov Chain Monte Carlo Sampling and Bootstrapping in assessing phylogenetic confidence. Mol. Biol. Evol. 20: 255-266. Allman, E. S. & Rhodes, J. A. 2004. Mathematical models in Biology: an introduction. Cambridge University Press, Cambridge, United Kingdom. APG 1998. An ordinal classification for the families of flowering plants. Ann. Missouri Bot. Gard. 85: 531-553. APG-II 2003. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Bot. J. Linn. Soc. 141: 399-436. Armbruster, W. S., Debevec, E. M. & Willson, M. F. 2002. Evolution of syncarpy in angiosperms: theoretical and phylogenetic analyses of the effects of carpel fusion on offspring quantity and quality. J. Evol. Biol. 15: 657-672. Aublet, F. 1775. Histoire des plantes de la Guiane françoise. Pierre-François Dodot jeune, London, Paris. Avise, J. C. & Johns, G. C. 1999. Proposal for a standardized temporal scheme of biological classification for extant species. Proc. Natl. Acad. Sci. USA 96: 7358-7363. Avise, J. C. 2000. Phylogeography. The history and formation of species. Harvard University Press, Cambridge, Massachusetts. Bachmann, K. 2001. Evolution and the genetic analysis of populations: 1950-2000. Taxon 50: 7-45. Backlund, A. & Bremer, K. 1998. To be or not to be - principles of classification and monotypic plant families.
    [Show full text]
  • Aristolochia Serpentaria L
    New England Plant Conservation Program Aristolochia serpentaria L. Virginia Snakeroot Conservation and Research Plan for New England Prepared by: Dorothy J. Allard, Ph.D. Analytical Resources, LLC P.O. Box 279 East Montpelier, VT 05651 For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, 2002 SUMMARY Aristolochia serpentaria L., commonly known as Virginia Snakeroot, is a perennial herb in the Aristolochiaceae. Several varieties have been described in the past, but they are no longer recognized in most taxonomic manuals. Aristolochia serpentaria occurs in 26 eastern states and is common in the southern and central part of its range, while becoming rare along its northern periphery. It is listed as a Division 2 species in Flora Conservanda (Brumback and Mehrhoff et al. 1996). Connecticut is the only New England state in which it is found, where it occurs at 12 known sites in ten towns. It grows in a variety of upland forest communities, but is more likely to be found in dry, somewhat rich, rocky, deciduous or mixed deciduous-coniferous woods in Connecticut. Farther south, it also has broad environmental requirements, occupying many upland soil and forest types. Population trends for the species in Connecticut are unclear. One new population was discovered in 2001. Monitoring in 2001 of eight extant sites found that two populations had decreased, three had increased, and one had stayed the same. Several known populations are threatened by habitat modification, invasive species, or site fragility. Two extant populations have not been surveyed for several years.
    [Show full text]
  • HOVERFLY NEWSLETTER Dipterists
    HOVERFLY NUMBER 41 NEWSLETTER SPRING 2006 Dipterists Forum ISSN 1358-5029 As a new season begins, no doubt we are all hoping for a more productive recording year than we have had in the last three or so. Despite the frustration of recent seasons it is clear that national and international study of hoverflies is in good health, as witnessed by the success of the Leiden symposium and the Recording Scheme’s report (though the conundrum of the decline in UK records of difficult species is mystifying). New readers may wonder why the list of literature references from page 15 onwards covers publications for the year 2000 only. The reason for this is that for several issues nobody was available to compile these lists. Roger Morris kindly agreed to take on this task and to catch up for the missing years. Each newsletter for the present will include a list covering one complete year of the backlog, and since there are two newsletters per year the backlog will gradually be eliminated. Once again I thank all contributors and I welcome articles for future newsletters; these may be sent as email attachments, typed hard copy, manuscript or even dictated by phone, if you wish. Please do not forget the “Interesting Recent Records” feature, which is rather sparse in this issue. Copy for Hoverfly Newsletter No. 42 (which is expected to be issued with the Autumn 2006 Dipterists Forum Bulletin) should be sent to me: David Iliff, Green Willows, Station Road, Woodmancote, Cheltenham, Glos, GL52 9HN, (telephone 01242 674398), email: [email protected], to reach me by 20 June 2006.
    [Show full text]
  • Anatomical Structure of Barks in Neotropical Genera of Annonaceae
    Ann. Bot. Fennici 44: 79–132 ISSN 0003-3847 Helsinki 28 March 2007 © Finnish Zoological and Botanical Publishing Board 2007 Anatomical structure of barks in Neotropical genera of Annonaceae Leo Junikka1 & Jifke Koek-Noorman2 1) Finnish Museum of Natural History, Botanical Museum, P.O. Box 7, FI-00014 University of Helsinki, Finland (present address: Botanic Garden, P.O. Box 44, FI-00014 University of Helsinki, Finland) (e-mail: [email protected]) 2) National Herbarium of the Netherlands, P.O. Box 80102, 3508 TC Utrecht, The Netherlands (e-mail: [email protected]) Received 1 Oct. 2004, revised version received 23 Aug. 2006, accepted 21 Jan. 2005 Junikka, L. & Koek-Noorman, J. 2007: Anatomical structure of barks in Neotropical genera of Annonaceae. — Ann. Bot. Fennici 44 (Supplement A): 79–132. The bark anatomy of 32 Neotropical genera of Annonaceae was studied. A family description based on Neotropical genera and a discussion of individual bark compo- nents are presented. Selected character states at the family and genus levels are sur- veyed for identification purposes. This is followed by a discussion on the taxonomical and phylogenetic relevance of bark characters according to a phylogram in preparation based on molecular characters. Although the value of many bark anatomical characters turned out to be insignificant in systematic studies of the family, some features lend support to recent phylogenetic results based on morphological and molecular data sets. The taxonomically most informative features of the bark anatomy are sclerification of phellem cells, shape of fibre groups and occurrence of crystals in bark components. Key words: anatomy, Annonaceae, bark, periderm, phloem, phylogeny, rhytidome, taxonomy Introduction collections and the development of some novel methods a multidisciplinary programme on Anno- Woody members of the Annonaceae are one of naceae was embarked on in 1983 at the Univer- the most species-rich components in the tropi- sity of Utrecht.
    [Show full text]
  • Aristolochic Acids Tract Urothelial Cancer Had an Unusually High Incidence of Urinary- Bladder Urothelial Cancer
    Report on Carcinogens, Fourteenth Edition For Table of Contents, see home page: http://ntp.niehs.nih.gov/go/roc Aristolochic Acids tract urothelial cancer had an unusually high incidence of urinary- bladder urothelial cancer. CAS No.: none assigned Additional case reports and clinical investigations of urothelial Known to be human carcinogens cancer in AAN patients outside of Belgium support the conclusion that aristolochic acids are carcinogenic (NTP 2008). The clinical stud- First listed in the Twelfth Report on Carcinogens (2011) ies found significantly increased risks of transitional-cell carcinoma Carcinogenicity of the urinary bladder and upper urinary tract among Chinese renal- transplant or dialysis patients who had consumed Chinese herbs or Aristolochic acids are known to be human carcinogens based on drugs containing aristolochic acids, using non-exposed patients as sufficient evidence of carcinogenicity from studies in humans and the reference population (Li et al. 2005, 2008). supporting data on mechanisms of carcinogenesis. Evidence of car- Molecular studies suggest that exposure to aristolochic acids is cinogenicity from studies in experimental animals supports the find- also a risk factor for Balkan endemic nephropathy (BEN) and up- ings in humans. per-urinary-tract urothelial cancer associated with BEN (Grollman et al. 2007). BEN is a chronic tubulointerstitial disease of the kidney, Cancer Studies in Humans endemic to Serbia, Bosnia, Croatia, Bulgaria, and Romania, that has The evidence for carcinogenicity in humans is based on (1) findings morphology and clinical features similar to those of AAN. It has been of high rates of urothelial cancer, primarily of the upper urinary tract, suggested that exposure to aristolochic acids results from consump- among individuals with renal disease who had consumed botanical tion of wheat contaminated with seeds of Aristolochia clematitis (Ivic products containing aristolochic acids and (2) mechanistic studies 1970, Hranjec et al.
    [Show full text]