Mountain Sweet Pitcher Plant Sarracenia Rubra Ssp
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Sarracenias Aquascapes Seed Grown Hybrids Dutch Treats Collector's
AQUASCAPES UNLIMITED, INC PO Box 364, Pipersville PA 18947 Phone: 215-766-8151, Fax: 215-766-8986 www.aquascapesunlimited.com EMAIL: [email protected] Spring 2014 Our Sarracenias are sold in small, medium and large sizes. The availability is indicated in the chart below with an X=Avail . The pricing reflects age and size: Small - $1.95 (1-2 Years) Multiples of 6, Medium - $3.95 (2-3 Years) Multiples of 5, Large - $8.95 (3-4Years) Multiples of 4. Sarracenias Botanical Name Common Name Small Med. Large Sarracenia alata Pale Pitcher X X X Sarracenia flava Yellow Trumpet X X Sarracenia leucophylla White Trumpet X X Sarracenia leucophylla 'Tarnock' ‘Tarnock’ X X Sarracenia psittacina Parrot Pitcher X Sarracenia purpurea Purple Pitcher X X X Sarracenia rubra Sweet Pitcher X X S. rubra ssp. jonesii (all green) Sweet Pitcher (all green) X Sarracenia x UNC Hybrid ‘Dixie Lace’ X X Sarracenia x UNC Hybrid ‘Doodle Bug’ X Sarracenia x UNC Hybrid ‘Mardi Gras’ X X Sarracenia x UNC Hybrid ‘Red Bug’ X Aquascapes Seed Grown Hybrids Sarracenia Hybrid Botanical Name Small Med. Large S. x areolata S. leucophylla x alata X X X S. x catesbaei S. purp x flava X X X S. readii x moorei S. (leuco x rubra j) (lxf) X X S. x readii All Green S. leuco x rubra jonsii X S. x moorei S. flava x leucophylla X S. x formosa (Limited) S. psitt x minor X Dutch Treats Botanical Name Common Name Size Price S. x 'Farnhamii ' Sarracenia x 'Farnhamii ' PL/72 3.95 S. -
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 -
(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. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Genetics of Sarracenia Leaf and Flower Color PHIL SHERIDAN
Genetics of Sarracenia leaf and flower color PHIL SHERIDAN Virginia Commonwealth Meadowview Biological Research University Station 8390 Fredericksburg Turnpike Department of Biology Woodford, VA 22580 816 Park Avenue Keywords: genetics: pigmentation-genetics: Sarracenia. Abstract Sarracenia is a genus of insectivorous plants confined to wetlands of eastern U.S. and Canada. Eight species are generally recognized with flower and leaf color ranging from yellow to red. Fertile hybrids occur in the wild under disturbed conditions and can be artificially produced in the greenhouse. Thus genetic barriers between species are weak. Normally when crosses occur or are induced between species or between different color types the progeny exhibit a blending of parental phenotypes called incomplete or partial dominance. In most species all-green mutants have been found which lack any red pigment in leaves, flowers or growth point. Controlled crosses were performed on all-green mutants from S. purpurea and two subspecies of the S. rubra complex. Self pollinated all-green plants Figure 1: A pink flowered hybrid in cultivation. This result in all-green offspring specimen was collected by Fred Case and is the cross S. and self pollinated wild-type rubra subsp. wherry) x S. alata. red plants result in red offspring. Crosses between red and all-green plants produce wild-type colored red progeny. These results suggest that the red alleles are "dominant" to the "recessive" all green mutant alleles in the three independent all-green variants tested. Since partial dominance is the usual genetic pattern in the genus, dominant/recessive characteristics are an unusual phenomenon. 1 Introduction The Sarraceniaceae (American pitcher plants) is a family of insectivorous pitcher plants restricted to wet, sunny, generally acid, nutrient poor habitats of the southeastern United States, Canada, northern California, southern Oregon, Venezuela, British Guiana (Lloyd, 1942), and Brazil (Maguire, 1978). -
The Long Overdue Recognition of Sarracenia Rubra Subsp. Viatorum
cpnl-47-04-06, PAGE 152, 10/05/18 Technical Refereed Contribution The long overdue recognition of Sarracenia rubra subsp. viatorum Barry A. Rice • Center for Plant Diversity • University of California • One Shields Avenue • Davis • California 95616 • USA • [email protected] Keywords: Taxonomy: Sarracenia rubra subsp. viatorum. Introduction The complex of taxa associated with Sarracenia rubra Walter has long been embroiled in contro- versy, with many scientists having different perspectives on how the plant should be interpreted. In part, this is because the plants have an interesting, patchy distribution throughout the southeastern USA. An early classification scheme of the plants under discussion was promoted by Case & Case (1974, 1976): Sarracenia rubra Walter Sarracenia jonesii Wherry Sarracenia alabamensis Case & R.B.Case Sarracenia alabamensis subsp. wherryi Case & R.B.Case Don Schnell, who I candidly observe was highly influential in my own thoughts on this, intro- duced a new name to recognize the plants along the Florida Gulf Coast: Sarracenia rubra Walter Sarracenia rubra subsp. jonesii (Wherry) Wherry Sarracenia rubra subsp. alabamensis (Case & R.B.Case) D.E.Schnell Sarracenia rubra subsp. wherryi (Case & R.B.Case) D.E.Schnell Sarracenia rubra subsp. gulfensis D.E.Schnell Looking at the names of scientists after the epithets, you see he did this by reducing the Case & Case “S. alabamensis” to subspecies status under S. rubra, and also transferred S. alabamensis subsp. wherryi to S. rubra. You can also see how even Wherry was uncertain how to deal with the S. rubra subsp. jonesii taxon, first having treated it as a species, and then as a subspecies. -
Carnivorous Plant Newsletter V47 N2 June 2018
An informal population report and observation of phenotypic variance and habitat of the Alabama Canebrake Pitcher Plant Sarracenia alabamensis Case & R.B. Case subsp. alabamensis (Sarraceniaceae) Noah D. Yawn • Helena High School • 1310 Hillsboro Parkway • Helena • Alabama • USA • [email protected] Abstract: Varying phenotypic traits of Sarracenia alabamensis Case & R.B. Case subsp. alabamen- sis (Sarraceniaceae), the Alabama Canebrake Pitcher Plant, were observed across its entire range. Listed under the U.S. Endangered Species Act, this rare, endemic species is currently limited to two counties across central Alabama. There is an undocumented phenotypic variability concern- ing pigmentation in five populations of Sarracenia alabamensis subsp. alabamensis across central Alabama. There appears to be higher levels of pigmentation in <5% of plants, characterized by a bi- lateral, interior ventral patch of anthocyanin pigmentation, terminating at the peristome and pitcher neck. Areolate and excess yellow coloration characteristics in these five populations, as well as net population status are reviewed and discussed. Introduction There is a total of five locations in two counties across central Alabama discussed in this report (Fig. 1), all visited within fall of 2016. Four visits occurred in the fall of 2017. Sarracenia alaba- mensis exhibits three main stages of growth during the active growing season. Beginning in mid to late April, the pitcher plants begin to bloom, producing multiple flowers per rhizomal growth point. Shortly after bloom, the first set of carnivorous leaves emerge, char- acterized by an enlarged ala, a perpendicular leaf “sail” on the anterior outside face of the pitcher tube. This en- larged ala, coinciding with significantly narrower pitcher tube diameters, results in spring growth being very floppy in nature. -
A Rare Plant Survey of Atlantic White-Cedar , Chamaecyparis Thyoides (L.) B.S.P., Habitats Of
A Rare Plant Survey of Atlantic White-Cedar , Chamaecyparis thyoides (L.) B.S.P., Habitats of the Georgia Westcentral Fall Line Sandhills Philip M. Sheridan1&2 and Thomas S. Patrick3 1Meadowview Biological Research Station, 8390 Fredericksburg Tnpk., Woodford, VA 22580, 2Old Dominion University, Department of Biological Sciences, Norfolk, VA 23529-0266, and 3Georgia Department of Natural Resources, Georgia Natural Heritage Program, 2117 U.S. Highway 278, S.E., Social Circle, Georgia 30025. Abstract The Georgia Westcentral Fall Line Sandhills are known for their local occurrences of rare and disjunct plant populations. Isolated stands of Atlantic white-cedar along clear, cool, sand- bottomed, spring-fed creeks associate with longleaf pine uplands. Together these two keystone species form the nucleus of a unique ecosystem in westcentral Georgia. During 1998 and 1999 a rare plant survey of Atlantic white-cedar habitats was performed. Typical rare plant species found with Atlantic white-cedar include Carex collinsii, Carex venusta, Fothergilla gardenii Helenium brevifolium, Kalmia carolina, Myriophyllum laxum, Pinguicula primuliflora, Sarracenia rubra, and Schoenoplectus etuberculatus. Noteworthy discoveries included Utricularia floridana, which has only been reported from Georgia in the Lake Seminole region, and a range extension for Macbridea caroliniana. The discovery of Chamaecyparis thyoides on a tributary formerly containing a population of Sarracenia oreophila represents a previously unrecognized plant association for this federally endangered pitcher plant species. New drainages containing Chamaecyparis thyoides were discovered on tributaries of Patsiliga, Beaver, and Horse creeks in Taylor County, Beaver Creek in Crawford County, Black Creek in Talbot County, and Shoal Creek in Marion County. Taken together these discoveries represent significant additions to the distributional knowledge of Atlantic white-cedar in westcentral Georgia. -
Carnivorous Plants Trap Them by Various Means, Depending on the Kind of Plant
ave you ever heard of meat-eating plants? Just like many animal species, some plant species are carnivorous—that is, they consume insects and other small animals for a primary source of nutrients and minerals for growth. Instead of actually eating insects, carnivorous plants trap them by various means, depending on the kind of plant. After animals such as flies, grasshoppers, and spiders are trapped, a pool of enzymes secreted by the plant digests the prey. arnivorous plants are found in many parts of the U.S., but are particularly abundant and diverse in some floodplains and small wetlands in the Southeast. Wetlands that are good for carnivorous plants generally have little or no drainage and low levels of essential plant nutrients. Nutrient-poor habitats typically have soils that are acidic or high in clay content; therefore, nutrients and minerals are not available in forms that are accessible to plants. The ability of carnivorous plants to capture and digest insects, supplemented by their capacity to make energy stores by photosynthesis as other green plants do, makes them highly competitive in nutrient-poor habitats. esearchers have discovered that not only do carnivorous plants depend upon the nutrition from devoured insects for survival, but some invertebrates also depend solely upon carnivorous plants for food and/or reproduction. In the Yellow Trumpet pitcher plant, Sarracenia flava, for example, some mosquito and other inspect species somehow evade capture and reproduce inside the rainwater-filled leaves. arnivorous plants are found in and near three wetland habitats that are increasingly rare due to impacts from mining, agriculture, and development. -
Energetics and the Evolution of Carnivorous Plants—Darwin’S ‘Most Wonderful Plants in the World’
Journal of Experimental Botany, Vol. 60, No. 1, pp. 19–42, 2009 doi:10.1093/jxb/ern179 DARWIN REVIEW Energetics and the evolution of carnivorous plants—Darwin’s ‘most wonderful plants in the world’ Aaron M. Ellison1,* and Nicholas J. Gotelli2 1 Harvard Forest, Harvard University, 324 North Main Street, Petersham, MA 01366, USA 2 Department of Biology, University of Vermont, 120 Marsh Life Sciences Building, Burlington, VT 05405, USA Received 6 May 2008; Revised 5 June 2008; Accepted 16 June 2008 Abstract Carnivory has evolved independently at least six times in five angiosperm orders. In spite of these independent origins, there is a remarkable morphological convergence of carnivorous plant traps and physiological convergence of mechanisms for digesting and assimilating prey. These convergent traits have made carnivorous plants model systems for addressing questions in plant molecular genetics, physiology, and evolutionary ecology. New data show that carnivorous plant genera with morphologically complex traps have higher relative rates of gene substitutions than do those with simple sticky traps. This observation suggests two alternative mechanisms for the evolution and diversification of carnivorous plant lineages. The ‘energetics hypothesis’ posits rapid morphological evolution resulting from a few changes in regulatory genes responsible for meeting the high energetic demands of active traps. The ‘predictable prey capture hypothesis’ further posits that complex traps yield more predictable and frequent prey captures. To evaluate these hypotheses, available data on the tempo and mode of carnivorous plant evolution were reviewed; patterns of prey capture by carnivorous plants were analysed; and the energetic costs and benefits of botanical carnivory were re-evaluated. -
Phylogeny and Biogeography of the Carnivorous Plant Family Sarraceniaceae Aaron M
University of Kentucky UKnowledge Regulatory Services Faculty Publications Regulatory Services 6-13-2012 Phylogeny and biogeography of the carnivorous plant family Sarraceniaceae Aaron M. Ellison Harvard University Elena D. Butler Harvard University Emily Jean Hicks University of Kentucky, [email protected] Robert F. C. Naczi The New York Botanical Garden Patrick J. Calie Eastern Kentucky University See next page for additional authors Right click to open a feedback form in a new tab to let us know how this document benefits oy u. Follow this and additional works at: https://uknowledge.uky.edu/regulatoryservices_facpub Part of the Agriculture Commons Repository Citation Ellison, Aaron M.; Butler, Elena D.; Hicks, Emily Jean; Naczi, Robert F. C.; Calie, Patrick J.; Bell, Charles D.; and Davis, Charles C., "Phylogeny and biogeography of the carnivorous plant family Sarraceniaceae" (2012). Regulatory Services Faculty Publications. 1. https://uknowledge.uky.edu/regulatoryservices_facpub/1 This Article is brought to you for free and open access by the Regulatory Services at UKnowledge. It has been accepted for inclusion in Regulatory Services Faculty Publications by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Authors Aaron M. Ellison, Elena D. Butler, Emily Jean Hicks, Robert F. C. Naczi, Patrick J. Calie, Charles D. Bell, and Charles C. Davis Phylogeny and biogeography of the carnivorous plant family Sarraceniaceae Notes/Citation Information Published in PLoS ONE, v. 7, no. 6, e39291. © 2012 Ellison et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
Teacher Guide to Georgia Sandhills
TEACHER GUIDE TO GEORGIA SANDHILLS TABLE OF CONTENTS SPONSORS . III ACKNOWLEDGMENTS . IV FOREWORD .. V HOW TO USE THIS GUIDE . VI SECTION 1: SANDHILL ECOSYSTEM OVERVIEW . 1 GEORGIA SANDHILLS FACT SHEET . 2 SANDHILL RETREAT . 5 SANDHILL RETREAT: A SIMULATED FIELD TRIP . 6 SANDHILLS FIRE ECOLOGY FACT SHEET . 9 PRESCRIBED FIRE Q & A . .11 FIRE IN THE SANDHILLS! . 14 SUCCESSION IN THE SANDHILLS - COPY PAGE . 17 PINE SEED HELICOPTERS - COPY PAGE . 18 SECTION 2: WILDLIFE OF THE SANDHILLS . 19 TORTOISE TROUBLES . 20 TORTOISE TROUBLES PLAYING FIELD DIAGRAM - COPY PAGE. 24 RESEARCH BIOLOGIST TALLY SHEET - COPY PAGE . 25 BURROW BUDDIES . 26 GOPHER TORTOISE AS THE KEYSTONE SPECIES IN THE SANDHILLS - COPY PAGE . 28 GOPHER TORTOISE BURROW WITH INHABITANTS - COPY PAGE . 29 GOPHER TORTOISE BURROW CROSS-SECTION - COPY PAGE . 31 BURROW BUDDIES FACT CARDS - COPY PAGE . 32 INTERVIEW A SANDHILL HERP . 38 SANDHILLS BIRD DETECTIVE . 40 SANDHILLS BIRD DETECTIVE FACT CARDS - COPY PAGE . 42 SECTION 3: PLANTS OF THE SANDHILLS . 49 COASTAL PLAIN PITCHERPLANT BOG FACT SHEET . 50 COASTAL PLAIN PLANT BOG DIVERSITY . 51 SANDHILL PLANTS ADAPTATION ARTISTRY . 53 SECTION 4: WILDLIFE FACT SHEETS . 57. BACHMAN’S SPARROW . 58 COTTON MOUSE . 60 EASTERN COTTONTAIL . 62 EASTERN DIAMONDBACK RATTLESNAKE. 64 i EASTERN FENCE LIZARD . 66 EASTERN INDIGO SNAKE . 68 EASTERN KINGSNAKE . 70 EASTERN SPADEFOOT TOAD . .72 GOPHER FROG . .74 GOPHER TORTOISE .. 76 GREAT BLUE HERON . 80 HISPID COTTON RAT . 82 NORTHERN BOBWHITE . 84 PINE SNAKE . 86 RED-COCKADED WOODPECKER . 88 RUBY-THROATED HUMMINGBIRD . 90 SOUTHEASTERN AMERICAN KESTREL . 92 SOUTHERN HOGNOSE SNAKE . 95 STRIPED NEWT . 97 STRIPED SKUNK . 99 APPENDICES . 101 A . ECOREGIONS OF GEORGIA MAPS .