Darlingtonia Jan—Mar
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Propagating with Nature: Simpler Is Better by Mike Creel Written for July 21, 2005 Workshop at the 22Nd Annual Cullowhee Conference “Native Plants in the Landscape
Propagating WITH Nature: Simpler Is Better By Mike Creel Written for July 21, 2005 workshop at The 22nd Annual Cullowhee Conference “Native Plants in the Landscape CONTENTS Page ---- Topics 1 -- Why You Came Here - To Learn Simple Propagation What Is Different About Creel-Way Propagation? Low-Tech, Simple, Outdoors, Cheap A Few “Technical Terms Why Learn to Propagate Native Plants 2 -- How to Get Started in Creel-Way Propagation Principles of Creel-Way Propagation When Sticking Cuttings When Planting Seed Pots Identification Tags Woody Cutting Theory 3 -- Selecting & Mixing Your Media One All-Purpose Media Mix Shade Cloth Cools Cuttings Just Local Humus, No Rooting Hormones, Repotting Cuttings Varmint Caps for Seed Pots 4 -- Drilling Pots To Improve Drainage Drilling Thin-Walled Plastic Rescuing Pots In Peril Hold-Down Wires 5 -- Selection And Use Of Propagation Domes 6 -- Cuttings by the Calendar - Winter, Spring, Summer, Fall 7 -- Cutting Selection for Native Azaleas and Other Plants Unusual Cutting Types - InstantPlant, SuperPlant Unorthodox Propagation Pots - High-Rise, Collander, Dome-Pot Potpourri 8 -- Propagator’s Review Propagation With Motivation, Advantages of Creel-Way My Latest Experiments, Several Rules Nature Is My Greenhouse, Sharing Your Fruits 9 -- American Native Azalea Species in Bloom Order for Southeast Photos and Illustrations 10 -- Creel-Way Dome-Pot one gallon 11 -- Recommended Pots & Domes 12 - -Drilling & Filling Pots for Good Drainage 13-- Menagerie of Dome-Pots 14 -- Collander Dome-Pot 15 -- Dormant Cuttings Are Really Pruning Mike Creel 155 Cannon Trail Road Lexington, South Carolina 29073 [email protected] 1 -- Propagating WITH Nature: Simpler Is Better by Mike Creel Why You Came - You have probably come to this workshop wanting to learn new, simpler ways to propagate native plants on a small scale, and you will! I do not use rooting hormones other than what is contained in the plant cutting and in local soil bacteria. -
Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae
OPEN ACCESS JCTS Article SERIES B Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae R.W. Sanders and T.C. Wood Core Academy of Science, Dayton, TN Abstract The morphological adaptations of carnivorous plants and taxonomic distributions of those adaptations are reviewed, as are the conflicting classifications of the plants based on the adaptations, reproductive morphology, and DNA sequences. To begin developing a creationist understanding of the origin of plant carnivory, we here focus specifically on pitcher plants of Nepenthaceae and Sarraceniaceae because their popularity as cultivated curiosities has generated a literature resource amenable to baraminological analysis. Hybridization records were augmented by total nucleotide differences to assess species similarities. Nonhybridizing species falling within the molecular range of hybridizing species were included in the monobaramin of the hybridizing species. The combined data support each of the three genera of the Sarraceniaceae as a monobaramin, but the three could not be combined into a larger monobaramin. With the Nepenthaceae, the data unequivocally place 73% of the species in a single monobaramin, strongly suggesting the whole genus (and, thus, family) is a monobaramin. The lack of variation in the carnivorous habit provides no evidence for the intrabaraminic origin of carnivory from non-carnivorous plants. An array of fascinating symbiotic relationships of pitchers in some species with unusual bacteria, insects, and vertebrates are known and suggest the origin of carnivory from benign functions of the adaptive structures. However, these symbioses still do not account for the apparent complex design for carnivory characteristic of all species in the two families. Editor: J.W. -
A Taxonomic Revision of Rhododendron L. Section Pentanthera G
A TAXONOMIC REVISION OF RHODODENDRON L. SECTION PENTANTHERA G. DON (ERICACEAE) BY KATHLEEN ANNE KRON A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 1987 , ACKNOWLEDGMENTS I gratefully acknowledge the supervision and encouragement given to me by Dr. Walter S. Judd. I thoroughly enjoyed my work under his direction. I would also like to thank the members of my advisory committee, Dr. Bijan Dehgan, Dr. Dana G. Griffin, III, Dr. James W. Kimbrough, Dr. Jonathon Reiskind, Dr. William Louis Stern, and Dr. Norris H. Williams for their critical comments and suggestions. The National Science Foundation generously supported this project in the form of a Doctoral Dissertation Improvement Grant;* field work in 1985 was supported by a grant from the Highlands Biological Station, Highlands, North Carolina. I thank the curators of the following herbaria for the loan of their material: A, AUA, BHA, DUKE, E, FSU, GA, GH, ISTE, JEPS , KW, KY, LAF, LE NCSC, NCU, NLU NO, OSC, PE, PH, LSU , M, MAK, MOAR, NA, , RSA/POM, SMU, SZ, TENN, TEX, TI, UARK, UC, UNA, USF, VDB, VPI, W, WA, WVA. My appreciation also is offered to the illustrators, Gerald Masters, Elizabeth Hall, Rosa Lee, Lisa Modola, and Virginia Tomat. I thank Dr. R. Howard * BSR-8601236 ii Berg for the scanning electron micrographs. Mr. Bart Schutzman graciously made available his computer program to plot the results of the principal components analyses. The herbarium staff, especially Mr. Kent D. Perkins, was always helpful and their service is greatly appreciated. -
Educational Posters on Threatened Plant Communities of North Carolina
Submitted by Nicolette L. Cagle on June 26, 2012 Native Plant Studies Certificate Project: Educational Posters on Threatened Plant Communities of North Carolina Nonriverine Wet Hardwood Forest from the Coastal Plain, NC. [Photo by David Blevins, Ph.D.] Submitted by Nicolette L. Cagle on June 26, 2012 Table of Contents Background ................................................................................................................................................... 3 Project Description........................................................................................................................................ 3 Timeline......................................................................................................................................................... 4 Most Threatened Plant Communities in North Carolina .............................................................................. 4 Poster Display at the North Carolina Botanical Garden................................................................................ 5 Posters .......................................................................................................................................................... 6 Introduction .............................................................................................................................................. 6 Threatened Plant Communities ................................................................................................................ 7 Poster Project References -
Carnivorous Plant Newsletter V42 N3 September 2013
Technical Refereed Contribution Phylogeny and biogeography of the Sarraceniaceae JOHN BRITTNACHER • Ashland, Oregon • USA • [email protected] Keywords: History: Sarraceniaceae evolution The carnivorous plant family Sarraceniaceae in the order Ericales consists of three genera: Dar- lingtonia, Heliamphora, and Sarracenia. Darlingtonia is represented by one species that is found in northern California and western Oregon. The genus Heliamphora currently has 23 recognized species all of which are native to the Guiana Highlands primarily in Venezuela with some spillover across the borders into Brazil and Guyana. Sarracenia has 15 species and subspecies, all but one of which are located in the southeastern USA. The range of Sarracenia purpurea extends into the northern USA and Canada. Closely related families in the plant order Ericales include the Roridu- laceae consisting of two sticky-leaved carnivorous plant species, Actinidiaceae, the Chinese goose- berry family, Cyrillaceae, which includes the common wetland plant Cyrilla racemiflora, and the family Clethraceae, which also has wetland plants including Clethra alnifolia. The rather charismatic plants of the Sarraceniaceae have drawn attention since the mid 19th century from botanists trying to understand how they came into being, how the genera are related to each other, and how they came to have such disjunct distributions. Before the advent of DNA sequencing it was very difficult to determine their relationships. Macfarlane (1889, 1893) proposed a phylogeny of the Sarraceniaceae based on his judgment of the overlap in features of the adult pitchers and his assumption that Nepenthes is a member of the family (Fig. 1a). He based his phy- logeny on the idea that the pitchers are produced from the fusion of two to five leaflets. -
Rhododendrons and Azaleas at Shore Acres
Overview Tips on Growing Rhodies and Azaleas All rhodies and azaleas are members Most azaleas and small-leaved rhodies of the genus Rhododendron. Azaleas Rhododendrons Rhodies and azaleas do not like “wet feet.” They prefer moist well- enjoy considerable sun in the Pacific differ from rhododendrons in that they Northwest if given adequate moisture can be evergreen or deciduous, while drained acid soil that contains lots of and Azaleas organic material. If your soil is a heavy during dry periods. Avoid hot spots like most rhodies are evergreen. They tend the south and west walls of buildings. However to have smaller leaves and flower clusters, clay-type, try to improve it by adding organic at Shore Acres material like compost or ground bark. Thoroughly the vast majority of rhodies and azaleas will as opposed to the larger flower trusses of not thrive in full or complete shade. More rhododendrons. Azaleas usually have 5-lobed dig or rototill in with the native soil. Do not totally replace the old soil with new material. shade promotes deeper green foliage but low flowers with 1 stamen per lobe, as opposed light intensity also reduces flower bud set to rhododendrons, which have 2 stamens per There should be a blend of native soil and soil amendments in the planting hole. If conditions and produces a leggier plant as it tries to find lobe. Other technical points that distinguish adequate sunshine. azaleas from rhododendrons are best left to are really challenging, consider a raised bed with those with microscopes. at least half of the root ball above the general ground level and good soil mounded around it. -
National List of Vascular Plant Species That Occur in Wetlands 1996
National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt. -
Evolutionary History of Floral Key Innovations in Angiosperms Elisabeth Reyes
Evolutionary history of floral key innovations in angiosperms Elisabeth Reyes To cite this version: Elisabeth Reyes. Evolutionary history of floral key innovations in angiosperms. Botanics. Université Paris Saclay (COmUE), 2016. English. NNT : 2016SACLS489. tel-01443353 HAL Id: tel-01443353 https://tel.archives-ouvertes.fr/tel-01443353 Submitted on 23 Jan 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. NNT : 2016SACLS489 THESE DE DOCTORAT DE L’UNIVERSITE PARIS-SACLAY, préparée à l’Université Paris-Sud ÉCOLE DOCTORALE N° 567 Sciences du Végétal : du Gène à l’Ecosystème Spécialité de Doctorat : Biologie Par Mme Elisabeth Reyes Evolutionary history of floral key innovations in angiosperms Thèse présentée et soutenue à Orsay, le 13 décembre 2016 : Composition du Jury : M. Ronse de Craene, Louis Directeur de recherche aux Jardins Rapporteur Botaniques Royaux d’Édimbourg M. Forest, Félix Directeur de recherche aux Jardins Rapporteur Botaniques Royaux de Kew Mme. Damerval, Catherine Directrice de recherche au Moulon Président du jury M. Lowry, Porter Curateur en chef aux Jardins Examinateur Botaniques du Missouri M. Haevermans, Thomas Maître de conférences au MNHN Examinateur Mme. Nadot, Sophie Professeur à l’Université Paris-Sud Directeur de thèse M. -
Rare Plants of Louisiana
Rare Plants of Louisiana Agalinis filicaulis - purple false-foxglove Figwort Family (Scrophulariaceae) Rarity Rank: S2/G3G4 Range: AL, FL, LA, MS Recognition: Photo by John Hays • Short annual, 10 to 50 cm tall, with stems finely wiry, spindly • Stems simple to few-branched • Leaves opposite, scale-like, about 1mm long, barely perceptible to the unaided eye • Flowers few in number, mostly born singly or in pairs from the highest node of a branchlet • Pedicels filiform, 5 to 10 mm long, subtending bracts minute • Calyx 2 mm long, lobes short-deltoid, with broad shallow sinuses between lobes • Corolla lavender-pink, without lines or spots within, 10 to 13 mm long, exterior glabrous • Capsule globe-like, nearly half exerted from calyx Flowering Time: September to November Light Requirement: Full sun to partial shade Wetland Indicator Status: FAC – similar likelihood of occurring in both wetlands and non-wetlands Habitat: Wet longleaf pine flatwoods savannahs and hillside seepage bogs. Threats: • Conversion of habitat to pine plantations (bedding, dense tree spacing, etc.) • Residential and commercial development • Fire exclusion, allowing invasion of habitat by woody species • Hydrologic alteration directly (e.g. ditching) and indirectly (fire suppression allowing higher tree density and more large-diameter trees) Beneficial Management Practices: • Thinning (during very dry periods), targeting off-site species such as loblolly and slash pines for removal • Prescribed burning, establishing a regime consisting of mostly growing season (May-June) burns Rare Plants of Louisiana LA River Basins: Pearl, Pontchartrain, Mermentau, Calcasieu, Sabine Side view of flower. Photo by John Hays References: Godfrey, R. K. and J. W. Wooten. -
(Sarracenia) Provide a 21St-Century Perspective on Infraspecific Ranks and Interspecific Hybrids: a Modest Proposal* for Appropriate Recognition and Usage
Systematic Botany (2014), 39(3) © Copyright 2014 by the American Society of Plant Taxonomists DOI 10.1600/036364414X681473 Date of publication 05/27/2014 Pitcher Plants (Sarracenia) Provide a 21st-Century Perspective on Infraspecific Ranks and Interspecific Hybrids: A Modest Proposal* for Appropriate Recognition and Usage Aaron M. Ellison,1,5 Charles C. Davis,2 Patrick J. Calie,3 and Robert F. C. Naczi4 1Harvard University, Harvard Forest, 324 North Main Street, Petersham, Massachusetts 01366, U. S. A. 2Harvard University Herbaria, Department of Organismic and Evolutionary Biology, 22 Divinity Avenue, Cambridge, Massachusetts 02138, U. S. A. 3Eastern Kentucky University, Department of Biological Sciences, 521 Lancaster Avenue, Richmond, Kentucky 40475, U. S. A. 4The New York Botanical Garden, 2900 Southern Boulevard, Bronx, New York 10458, U. S. A. 5Author for correspondence ([email protected]) Communicating Editor: Chuck Bell Abstract—The taxonomic use of infraspecific ranks (subspecies, variety, subvariety, form, and subform), and the formal recognition of interspecific hybrid taxa, is permitted by the International Code of Nomenclature for algae, fungi, and plants. However, considerable confusion regarding the biological and systematic merits is caused by current practice in the use of infraspecific ranks, which obscures the meaningful variability on which natural selection operates, and by the formal recognition of those interspecific hybrids that lack the potential for inter-lineage gene flow. These issues also may have pragmatic and legal consequences, especially regarding the legal delimitation and management of threatened and endangered species. A detailed comparison of three contemporary floras highlights the degree to which infraspecific and interspecific variation are treated inconsistently. -
Delete Darlingtonia Californica from Appendix II
Prop. 11.11 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II Proposals resulting from reviews by the Plants Committees A. Proposal Delete Darlingtonia californica from Appendix II. B. Proponent Swiss Confederation. C. Supporting Statement 1. Taxonomy 1.1 Class: Dicotyledonae 1.2 Order: Nepenthales 1.3 Family: Sarraceniaceae 1.4 Genus: Darlingtonia 1.4.1: Species: Darlingtonia californica Torrey 1.5 Scientific synonyms: 1.6 Common names: English: California pitcherplant, cobra lily French: Spanish: 1.7 Code numbers: 2. Biological Parameters 2.1 Distribution USA, West Coast, from Oregon to North California on a 160 km long strip between Roseburg (Oregon) and Santa Rosa (California). Along the coast, it appears in northern Curry County and extends north sporadically to Sandlake in Tillamook County. 2.2 Habitat availability From sea level to 2800 m. 2.3 Population status In the center of its range from Del Norte-Trinity-Shasta-Siskiyou County (California) to Curry & Josephine County (Oregon) this species is rather abundant. It is not uncommon throughout this area to find several colonies numbering between 1000-3000 specimens with abundant habitat for expansion and few threats to their survival because many locations are very difficult to access (Rondeau, pers.comm. to von Arx, 1999). At the southern limit of its range in Nevada County it is quite abundant and grows on remote sites; while in 3 nearby Counties (Butte, Plumas and Sierra) it has never been abundant, and it is now scattered and diminishing due to the combined effects of logging and succession into other vegetation types. Prop. 11.11 – p. -
The Cost of Carnivory for Darlingtonia Californica (Sarraceniaceae): Evidence from Relationships Among Leaf Traits1
American Journal of Botany 92(7): 1085±1093. 2005. THE COST OF CARNIVORY FOR DARLINGTONIA CALIFORNICA (SARRACENIACEAE): EVIDENCE FROM RELATIONSHIPS AMONG LEAF TRAITS1 AARON M. ELLISON2,4 AND ELIZABETH J. FARNSWORTH3 2Harvard University, Harvard Forest, P.O. Box 68, Petersham, Massachusetts 01366 USA; and 3New England Wild Flower Society, 180 Hemenway Road, Framingham, Massachusetts 01701 USA Scaling relationships among photosynthetic rate, foliar nutrient concentration, and leaf mass per unit area (LMA) have been observed for a broad range of plants. Leaf traits of the carnivorous pitcher plant Darlingtonia californica, endemic to southern Oregon and northern California, USA, differ substantially from the predictions of these general scaling relationships; net photosynthetic rates of Darlingtonia are much lower than predicted by general scaling relationships given observed foliar nitrogen (N) and phosphorus (P) concentrations and LMA. At ®ve sites in the center of its range, leaf traits of Darlingtonia were strongly correlated with elevation and differed with soil calcium availability and bedrock type. The mean foliar N : P of 25.2 6 15.4 of Darlingtonia suggested that these plants were P-limited, although N concentration in the substrate also was extremely low and prey capture was uncommon. Foliar N : P stoichiometry and the observed deviation of Darlingtonia leaf traits from predictions of general scaling relationships permit an initial assessment of the ``cost of carnivory'' in this species. Carnivory in plants is thought to have evolved in response to N limitation, but for Darlingtonia, carnivory is an evolutionary last resort when both N and P are severely limiting and photosynthesis is greatly reduced. Key words: carnivorous plants; Darlingtonia californica; fens; leaf mass area; leaf traits; photosynthesis; nitrogen; serpentine.