Points covered in this factsheet Symptoms Planting problems Physiological effects Environmental, Soil and Climate factors Insect, Disease and Vertebrate agents Dying Cedar Hedges —What Is The Cause? Attractive and normally trouble free, cedar trees can be great additions to the landscape. Dieback of cedar hedging in the landscape is a common prob- lem. In most cases, it is not possible to pinpoint one single cause. Death is usually the result of a combination of envi- ronmental stresses, soil factors and problems originating at planting. Disease, insect or animal injury is a less frequent cause. Identifying The Host Certain species of cedar are susceptible to certain problems, so identifying the host plant can help to identify the cause and whether a symptom is an issue of concern or is normal for that plant. The most common columnar hedging cedars are Thuja plicata (Western Red Cedar - native to the West Coast) and Thuja occidentalis (American Arborvitae or Eastern White ICULTURE, PLANT HEALTH UNIT Cedar). Both species are often called arborvitae. Common varieties of Western Red ce- dar are ‘Emerald Giant’, ‘Excelsa’ and Atrovirens’. ‘Smaragd’ and ‘Pyramidalis’ are com- mon varieties of Eastern White cedar hedging. Species of Cupressus (Cypress), Chamaecyparis nootkatensis (Yellow Cedar or False Cypress) and Chamaecyparis law- soniana (Port Orford Cedar or lawsom Cypress) are also used in hedging. Symptoms The pattern of symptom development/distribution can provide a clue to whether the prob- lem is biotic (infectious) or abiotic (non-infectious). Trees often die out in a group, in one section of the hedge, or at random throughout the hedge.
Thuja Occidentalis) Swamps in Northern New York: Effects and Interactions of Multiple Variables
SUNY College of Environmental Science and Forestry Digital Commons @ ESF Dissertations and Theses Fall 12-16-2017 Plant Species Richness and Diversity of Northern White-Cedar (Thuja occidentalis) Swamps in Northern New York: Effects and Interactions of Multiple Variables Robert Smith SUNY College of Environmental Science and Forestry, rlsmit08@syr.edu Follow this and additional works at: https://digitalcommons.esf.edu/etds Recommended Citation Smith, Robert, "Plant Species Richness and Diversity of Northern White-Cedar (Thuja occidentalis) Swamps in Northern New York: Effects and Interactions of Multiple Variables" (2017). Dissertations and Theses. 7. https://digitalcommons.esf.edu/etds/7 This Open Access Thesis is brought to you for free and open access by Digital Commons @ ESF. It has been accepted for inclusion in Dissertations and Theses by an authorized administrator of Digital Commons @ ESF. For more information, please contact digitalcommons@esf.edu, cjkoons@esf.edu. PLANT SPECIES RICHNESS AND DIVERSITY OF NORTHERN WHITE-CEDAR (Thuja occidentalis) SWAMPS IN NORTHERN NEW YORK: EFFECTS AND INTERACTIONS OF MULTIPLE VARIABLES by Robert L. Smith II A thesis submitted in partial fulfillment of the requirements for the Master of Science Degree State University of New York College of Environmental Science and Forestry Syracuse, New York November 2017 Department of Environmental and Forest Biology Approved by: Donald J. Leopold, Major Professor René H. Germain, Chair, Examining Committee Donald J. Leopold, Department Chair S. Scott Shannon, Dean, The Graduate School ACKNOWLEDGEMENT I would like to thank my major professor, Dr. Donald J. Leopold, for his great advice during our many meetings and email exchanges. In addition, his visit to my study site and recommended improvements to my thesis were very much appreciated.
Behavioral Responses of American Black Bears to Reduced Natural Foods: Home Range Size and Seasonal Migrations
BEHAVIORAL RESPONSES OF AMERICAN BLACK BEARS TO REDUCED NATURAL FOODS: HOME RANGE SIZE AND SEASONAL MIGRATIONS Spencer J. Rettler1, David L. Garshelis, Andrew N. Tri, John Fieberg1, Mark A. Ditmer2 and James Forester1 SUMMARY OF FINDINGS American black bears (Ursus americanus) in the Chippewa National Forest demonstrated appreciable fat reserves and stable reproduction despite a substantial decline in natural food availability over a 30-year period. Here we investigated potential strategies that bears may have employed to adapt to this reduction in food. We hypothesized that bears increased their home range sizes to encompass more food and/or increased the frequency, duration and distance of large seasonal migrations to seek out more abundant food resources. We estimated home range sizes using both Minimum Convex Polygon and Kernel Density Estimate approaches and developed a method to identify seasonal migrations. Male home range sizes in the 2010s were approximately twice the size of those in the 1980s; whereas, female home ranges tripled in size from the 1980s to the 2010s. We found little difference in migration patterns with only slight changes to duration. Our results supported our hypothesis that home range size increased in response to declining foods, which may explain why body condition and reproduction has not changed. However, these increased movements, in conjunction with bears potentially consuming more human-related foods in the fall, may alter harvest vulnerability, and should be considered when managing the bear hunt. INTRODUCTION As a large generalist omnivore, American black bears (Ursus americanus; henceforth black bear or bear) demonstrate exceptional plasticity in response to changes in food availability.
Case Study of Anatomy, Physical and Mechanical Properties of the Sapwood and Heartwood of Random Tree Platycladus Orientalis (L.) Franco from South-Eastern Poland
Article Case Study of Anatomy, Physical and Mechanical Properties of the Sapwood and Heartwood of Random Tree Platycladus orientalis (L.) Franco from South-Eastern Poland Agnieszka Laskowska * , Karolina Majewska, Paweł Kozakiewicz , Mariusz Mami ´nskiand Grzegorz Bryk The Institute of Wood Sciences and Furniture, 159 Nowoursynowska St., 02-776 Warsaw, Poland; carolina9703@wp.pl (K.M.); pawel_kozakiewicz@sggw.edu.pl (P.K.); mariusz_maminski@sggw.edu.pl (M.M.); gbryk@onet.pl (G.B.) * Correspondence: agnieszka_laskowska@sggw.edu.pl Abstract: Oriental arborvitae is not fully characterized in terms of its microscopic structure or physical or mechanical properties. Moreover, there is a lot of contradictory information in the literature about oriental arborvitae, especially in terms of microscopic structure. Therefore, the sapwood (S) and heartwood (H) of Platycladus orientalis (L.) Franco from Central Europe were subjected to examinations. The presence of helical thickenings was found in earlywood tracheids (E). Latewood tracheids (L) were characterized by a similar thickness of radial and tangential walls and a similar diameter in the tangential direction in the sapwood and heartwood zones. In the case of earlywood tracheids, such a similarity was found only in the thickness of the tangential walls. The volume swelling (VS) of sapwood and heartwood after reaching maximum moisture content (MMC) was 12.8% (±0.5%) and 11.2% (±0.5%), respectively. The average velocity of ultrasonic Citation: Laskowska, A.; Majewska, waves along the fibers (υ) for a frequency of 40 kHz was about 6% lower in the heartwood zone K.; Kozakiewicz, P.; Mami´nski,M.; than in the sapwood zone. The dynamic modulus of elasticity (MOED) was about 8% lower in the Bryk, G.
Morphology and Morphogenesis of the Seed Cones of the Cupressaceae - Part II Cupressoideae
1 2 Bull. CCP 4 (2): 51-78. (10.2015) A. Jagel & V.M. Dörken Morphology and morphogenesis of the seed cones of the Cupressaceae - part II Cupressoideae Summary The cone morphology of the Cupressoideae genera Calocedrus, Thuja, Thujopsis, Chamaecyparis, Fokienia, Platycladus, Microbiota, Tetraclinis, Cupressus and Juniperus are presented in young stages, at pollination time as well as at maturity. Typical cone diagrams were drawn for each genus. In contrast to the taxodiaceous Cupressaceae, in Cupressoideae outgrowths of the seed-scale do not exist; the seed scale is completely reduced to the ovules, inserted in the axil of the cone scale. The cone scale represents the bract scale and is not a bract- /seed scale complex as is often postulated. Especially within the strongly derived groups of the Cupressoideae an increased number of ovules and the appearance of more than one row of ovules occurs. The ovules in a row develop centripetally. Each row represents one of ascending accessory shoots. Within a cone the ovules develop from proximal to distal. Within the Cupressoideae a distinct tendency can be observed shifting the fertile zone in distal parts of the cone by reducing sterile elements. In some of the most derived taxa the ovules are no longer (only) inserted axillary, but (additionally) terminal at the end of the cone axis or they alternate to the terminal cone scales (Microbiota, Tetraclinis, Juniperus). Such non-axillary ovules could be regarded as derived from axillary ones (Microbiota) or they develop directly from the apical meristem and represent elements of a terminal short-shoot (Tetraclinis, Juniperus).
Family: Cupressaceae Taxon: Thuja x 'Green Giant' Synonym: Thuja plicata J. Donn ex D. Don x Thuja stan Common Name: 'Green Giant' Questionaire : current 20090513 Assessor: Chuck Chimera Designation: L Status: Assessor Approved Data Entry Person: Chuck Chimera WRA Score -14 101 Is the species highly domesticated? y=-3, n=0 y 102 Has the species become naturalized where grown? y=1, n=-1 n 103 Does the species have weedy races? y=1, n=-1 n 201 Species suited to tropical or subtropical climate(s) - If island is primarily wet habitat, then (0-low; 1-intermediate; 2- Low substitute "wet tropical" for "tropical or subtropical" high) (See Appendix 2) 202 Quality of climate match data (0-low; 1-intermediate; 2- Low high) (See Appendix 2) 203 Broad climate suitability (environmental versatility) y=1, n=0 y 204 Native or naturalized in regions with tropical or subtropical climates y=1, n=0 n 205 Does the species have a history of repeated introductions outside its natural range? y=-2, ?=-1, n=0 ? 301 Naturalized beyond native range y = 1*multiplier (see n Appendix 2), n= question 205 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see n Appendix 2) 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see n Appendix 2) 304 Environmental weed n=0, y = 2*multiplier (see n Appendix 2) 305 Congeneric weed n=0, y = 1*multiplier (see Appendix 2) 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic y=1, n=0 403 Parasitic y=1, n=0 n 404 Unpalatable to grazing animals y=1, n=-1 405 Toxic to animals y=1, n=0 n 406 Host
Vol. XV DECEMBER, 1914 No. 180 JOURNAL The New York Botanical Garden EDITOR ARLOW BURDETTE STOUT Director of the Laboratories CONTENTS PAGE Index to Volumes I-XV »33 PUBLISHED FOR THE GARDEN AT 41 NORTH QUBKN STRHBT, LANCASTER, PA. THI NEW ERA PRINTING COMPANY OFFICERS 1914 PRESIDENT—W. GILMAN THOMPSON „ „ _ i ANDREW CARNEGIE VICE PRESIDENTS J FRANCIS LYNDE STETSON TREASURER—JAMES A. SCRYMSER SECRETARY—N. L. BRITTON BOARD OF- MANAGERS 1. ELECTED MANAGERS Term expires January, 1915 N. L. BRITTON W. J. MATHESON ANDREW CARNEGIE W GILMAN THOMPSON LEWIS RUTHERFORD MORRIS Term expire January. 1916 THOMAS H. HUBBARD FRANCIS LYNDE STETSON GEORGE W. PERKINS MVLES TIERNEY LOUIS C. TIFFANY Term expire* January, 1917 EDWARD D. ADAMS JAMES A. SCRYMSER ROBERT W. DE FOREST HENRY W. DE FOREST J. P. MORGAN DANIEL GUGGENHEIM 2. EX-OFFICIO MANAGERS THE MAYOR OP THE CITY OF NEW YORK HON. JOHN PURROY MITCHEL THE PRESIDENT OP THE DEPARTMENT OP PUBLIC PARES HON. GEORGE CABOT WARD 3. SCIENTIFIC DIRECTORS PROF. H. H. RUSBY. Chairman EUGENE P. BICKNELL PROF. WILLIAM J. GIES DR. NICHOLAS MURRAY BUTLER PROF. R. A. HARPER THOMAS W. CHURCHILL PROF. JAMES F. KEMP PROF. FREDERIC S. LEE GARDEN STAFF DR. N. L. BRITTON, Director-in-Chief (Development, Administration) DR. W. A. MURRILL, Assistant Director (Administration) DR. JOHN K. SMALL, Head Curator of the Museums (Flowering Plants) DR. P. A. RYDBERG, Curator (Flowering Plants) DR. MARSHALL A. HOWE, Curator (Flowerless Plants) DR. FRED J. SEAVER, Curator (Flowerless Plants) ROBERT S. WILLIAMS, Administrative Assistant PERCY WILSON, Associate Curator DR. FRANCIS W. PENNELL, Associate Curator GEORGE V.
Tel: 503.628.8685 Fax: 503.628.1426 www.eshraghinursery.com 1 Eshraghi’s TOP 10 picks Our locations 1 Main Office, Shipping & Growing 2 Retail Store & Growing 26985 SW Farmington Road Farmington Gardens Hillsboro, OR 97123 21815 SW Farmington Road Beaverton, OR 97007 1 2 3 7 6 3 River Ranch Facility 4 Liberty Farm 4 5 10 N SUNSET HWY TO PORTLAND 8 9 TU HILLSBORO ALA TIN 26 VALL SW 185TH AVE. EY HWY. #4 8 BEAVERTON TONGUE LN. GRABEL RD . D R . E D G R ID E ALOHA R G B D I R R #3 SW 209TH E B T D FARMINGTON ROAD D N A I SIMPSON O O M O R R 10 217 ROSEDALE W R E S W V S I R N W O 219 T K C A J #2 #1 SW UNGER RD. SW 185TH AVE. 1 Acer circinatum ‘Pacific Fire’ (Vine Maple), page 6 D A SW MURRAY BLVD. N RO 2 palmatum (Japanese Maple), NGTO Acer 'Geisha Gone Wild' page 8 FARMI 3 Acer palmatum 'Mikawa yatsubusa' (Japanese Maple), page 10 #1 4 Acer palmatum dissectum 'Orangeola' (Japanese Maple), page 14 5 Hydrangea macrophylla 'McKay', Cherry Explosion PP28757 (Hydrangea), page 32 6 Picea glauca 'Eshraghi1', Poco Verde (White Spruce), page 61 ROAD HILL CLARK 7 Picea pungens 'Hockersmith', Linda (Colorado Spruce), page 64 RY ROAD 8 Pinus nigra 'Green Tower' (Austrian Pine), page 65 SCHOLLS FER 9 Thuja occidentalis 'Janed Gold', Highlights™ PP21967 (Arborvitae), page 70 10 Thuja occidentalis 'Anniek', Sienna Sunset™ (Arborvitae), page 69 Table of contents Tags Make a Difference .
Combatting the Urban Heat Island Effect: What Trees Are Suitable for Atlanta’s Current and Future Climate? An Applied Research Paper Written by: Anna Baggett Supervised by: Dr. Brian Stone Spring 2019 Acknowledgements This report was prepared for Georgia Tech’s School of City and Regional Planning as a part of its applied research paper requirement. This paper would not have been possible without the support of Dr. Brian Stone who supervised its writing. The author would also like to thank Alex Beasley and Mike McCord at Trees Atlanta for generously offering tree species lists. Cover photo credit: 1460daysofgeorgia.wordpress.com Back cover photo credit: ATLnature Table of Contents INTRODUCTION ......................................................................................................................... 1 LITERATURE REVIEW ............................................................................................................2 Trees and the UHI Effect ............................................................................................2 Shifting Plant Hardiness Zones .........................................................................3 Future Climates and Tree Planting ..................................................................4 Gaps in Current Literature ......................................................................................4 METHODS.......................................................................................................................................5 Hardiness Zones ..............................................................................................................5
Supporting Information Mao et al. 10.1073/pnas.1114319109 SI Text BEAST Analyses. In addition to a BEAST analysis that used uniform Selection of Fossil Taxa and Their Phylogenetic Positions. The in- prior distributions for all calibrations (run 1; 144-taxon dataset, tegration of fossil calibrations is the most critical step in molecular calibrations as in Table S4), we performed eight additional dating (1, 2). We only used the fossil taxa with ovulate cones that analyses to explore factors affecting estimates of divergence could be assigned unambiguously to the extant groups (Table S4). time (Fig. S3). The exact phylogenetic position of fossils used to calibrate the First, to test the effect of calibration point P, which is close to molecular clocks was determined using the total-evidence analy- the root node and is the only functional hard maximum constraint ses (following refs. 3−5). Cordaixylon iowensis was not included in in BEAST runs using uniform priors, we carried out three runs the analyses because its assignment to the crown Acrogymno- with calibrations A through O (Table S4), and calibration P set to spermae already is supported by previous cladistic analyses (also [306.2, 351.7] (run 2), [306.2, 336.5] (run 3), and [306.2, 321.4] using the total-evidence approach) (6). Two data matrices were (run 4). The age estimates obtained in runs 2, 3, and 4 largely compiled. Matrix A comprised Ginkgo biloba, 12 living repre- overlapped with those from run 1 (Fig. S3). Second, we carried out two runs with different subsets of sentatives from each conifer family, and three fossils taxa related fi to Pinaceae and Araucariaceae (16 taxa in total; Fig.