Live-Oak-Publication Set-Two
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CITIZEN SCIENTIST PROGRAM Southern California Oak Resource Assessment Reference Guide
CITIZEN SCIENTIST PROGRAM Southern California Oak Resource Assessment Reference Guide Forest Health Protection, Region 5 and University of California,1 Riverside Table of Contents New threats to forest health are commonly first diagnosed in urban environments and initially discovered by concerned citizens. Early detection of introduced/exotic pests can assist with mitigating these new threats. The southern oak woodlands of Califor- nia represent crucial habitat for plants and wildlife, improve ecosystem services, and contribute to aesthetics. Observations by citizens can assist with protecting these valuable woodlands. This reference guide was developed to provide an overview of common injury symp- toms from insects and diseases to oaks in southern California. The guide is parti- tioned into feeding guilds and injury types with less emphasis on identifying specific insect and pathogen species. Injury symptoms can assist with identifying the specific problem and level of severity. This guide should be used jointly with the Southern California Citizen Scientist Survey Form. Headings Page Oak Species of Southern California 3-7 Injury Ratings for Oak Canopies 8 Common Insect Injury Classes Wood Boring 9-11 Bark Feeding 12-13 Leaf Feeding 14-15 Sucking Insects 16-17 Common Disease Injury Classes Cankers, Wetwood, and Stem Decays 18-19 Leaf and Twig Diseases and Mistletoe 20-21 Severity Ratings for Injury Symptoms 22 Additional information 23 2 Common Oak Species Coast live oak (Quercus agrifolia) This is an evergreen oak species with a broad crown and smooth bark that is common in urban and for- est settings. Leaves are leathery and cupped or flat shaped with margins spiny or round. -
Native Trees of Georgia
1 NATIVE TREES OF GEORGIA By G. Norman Bishop Professor of Forestry George Foster Peabody School of Forestry University of Georgia Currently Named Daniel B. Warnell School of Forest Resources University of Georgia GEORGIA FORESTRY COMMISSION Eleventh Printing - 2001 Revised Edition 2 FOREWARD This manual has been prepared in an effort to give to those interested in the trees of Georgia a means by which they may gain a more intimate knowledge of the tree species. Of about 250 species native to the state, only 92 are described here. These were chosen for their commercial importance, distribution over the state or because of some unusual characteristic. Since the manual is intended primarily for the use of the layman, technical terms have been omitted wherever possible; however, the scientific names of the trees and the families to which they belong, have been included. It might be explained that the species are grouped by families, the name of each occurring at the top of the page over the name of the first member of that family. Also, there is included in the text, a subdivision entitled KEY CHARACTERISTICS, the purpose of which is to give the reader, all in one group, the most outstanding features whereby he may more easily recognize the tree. ACKNOWLEDGEMENTS The author wishes to express his appreciation to the Houghton Mifflin Company, publishers of Sargent’s Manual of the Trees of North America, for permission to use the cuts of all trees appearing in this manual; to B. R. Stogsdill for assistance in arranging the material; to W. -
Oaks (Quercus Spp.): a Brief History
Publication WSFNR-20-25A April 2020 Oaks (Quercus spp.): A Brief History Dr. Kim D. Coder, Professor of Tree Biology & Health Care / University Hill Fellow University of Georgia Warnell School of Forestry & Natural Resources Quercus (oak) is the largest tree genus in temperate and sub-tropical areas of the Northern Hemisphere with an extensive distribution. (Denk et.al. 2010) Oaks are the most dominant trees of North America both in species number and biomass. (Hipp et.al. 2018) The three North America oak groups (white, red / black, and golden-cup) represent roughly 60% (~255) of the ~435 species within the Quercus genus worldwide. (Hipp et.al. 2018; McVay et.al. 2017a) Oak group development over time helped determine current species, and can suggest relationships which foster hybridization. The red / black and white oaks developed during a warm phase in global climate at high latitudes in what today is the boreal forest zone. From this northern location, both oak groups spread together southward across the continent splitting into a large eastern United States pathway, and much smaller western and far western paths. Both species groups spread into the eastern United States, then southward, and continued into Mexico and Central America as far as Columbia. (Hipp et.al. 2018) Today, Mexico is considered the world center of oak diversity. (Hipp et.al. 2018) Figure 1 shows genus, sub-genus and sections of Quercus (oak). History of Oak Species Groups Oaks developed under much different climates and environments than today. By examining how oaks developed and diversified into small, closely related groups, the native set of Georgia oak species can be better appreciated and understood in how they are related, share gene sets, or hybridize. -
Quercus Acutissima (Sawtooth Oak)
Green Gone Bad Featured Ornamental Plant: Quercus acutissima (Sawtooth Oak) Some exotic ornamental plants behave badly when they escape from the place they are planted. Infestations of these plants have negative impacts on natural environments. One of these plants is Quercus acutissima; common name: Sawtooth oak. Quercus acutissima is medium to large deciduous tree in the family Fagaceae. It is native to Asia but has been widely planted in the United States as an ornamental and as food for wildlife. Particular varieties have been developed for the abundant production of acorns early in the life of the tree. Quercus acutissima has recently begun invading forests in the eastern United States. Quercus acutissima grows up to 50 feet tall and forms a dense pyramidal crown that rounds with age. Leaves are alternate, simple, lanceolate, 3 to 7 inches long, pinnately veined with a very sharply serrate margin bearing bristle-tipped teeth. The leaves resemble some native tree species including American chestnut, Alleghany chinkapin, American beech, as well as the non-native Chinese chestnut. Acorns are oval with a cap that covers 1/2 of the nut with prominently curved scales resembling hair. Twigs are slender, red to gray-brown with multiple pubescent terminal buds. Mature bark is ridged, furrowed, and somewhat corky. The problem with Quercus acutissima is that it can escape from planted landscapes into natural areas. Early mast production has led to widespread planting of sawtooth oak as a wildlife food tree in natural areas and parks. Due to the large crop of acorns, this species can out-compete the seedlings of native oaks and other species, ultimately reducing plant diversity and wildlife habitat quality. -
The Founding Member Trees of the Live Oak Society
Survivors—the Founding Member Trees of the Live Oak Society William Guion www.williamguion.com 831.224.2962 In South Louisiana, the landscape lies flat as cut sugarcane. Here, the sprawling shape of a live oak tree can dominate the view for miles. By the sight of a familiar oak you can tell where you’re going, where you’d been, and how much farther you have to go before you reach your destination. Live oaks are heritage, heirlooms, and history all rolled into one. On the old land maps, oaks marked where one property line ended and another began. They were a point on the horizon to aim the blade of a plow or the nose of a tractor. They mark where back roads cross and provide a shady spot where neighbors can park their pickups, pass a plastic thermos cup of chicory coffee, and discuss the weather. Duels were fought and honor won or lost under their bowed limbs. People picnic under them, get married under them, dance the two-step under them, and finally when the music ends, are laid to rest alongside their massive roots. In April 1934, Dr. Edwin Lewis Stephens, the first president of the Southwestern Louisiana Institute (now University of Louisiana at Lafayette), published an article in the Louisiana Conservation Review titled, “I Saw in Louisiana a Live Oak Growing.” The piece drew its name from a poem by Walt Whitman, and like Whitman’s poem, Stephens praised the singular beauty of this distinctly Southern species of oak (Quercus virginiana). His appreciation for live oaks grew over many years of being raised and living in Louisiana and from frequent motor trips he took with his wife along the back roads and byways through Cajun country. -
ISB: Atlas of Florida Vascular Plants
Longleaf Pine Preserve Plant List Acanthaceae Asteraceae Wild Petunia Ruellia caroliniensis White Aster Aster sp. Saltbush Baccharis halimifolia Adoxaceae Begger-ticks Bidens mitis Walter's Viburnum Viburnum obovatum Deer Tongue Carphephorus paniculatus Pineland Daisy Chaptalia tomentosa Alismataceae Goldenaster Chrysopsis gossypina Duck Potato Sagittaria latifolia Cow Thistle Cirsium horridulum Tickseed Coreopsis leavenworthii Altingiaceae Elephant's foot Elephantopus elatus Sweetgum Liquidambar styraciflua Oakleaf Fleabane Erigeron foliosus var. foliosus Fleabane Erigeron sp. Amaryllidaceae Prairie Fleabane Erigeron strigosus Simpson's rain lily Zephyranthes simpsonii Fleabane Erigeron vernus Dog Fennel Eupatorium capillifolium Anacardiaceae Dog Fennel Eupatorium compositifolium Winged Sumac Rhus copallinum Dog Fennel Eupatorium spp. Poison Ivy Toxicodendron radicans Slender Flattop Goldenrod Euthamia caroliniana Flat-topped goldenrod Euthamia minor Annonaceae Cudweed Gamochaeta antillana Flag Pawpaw Asimina obovata Sneezeweed Helenium pinnatifidum Dwarf Pawpaw Asimina pygmea Blazing Star Liatris sp. Pawpaw Asimina reticulata Roserush Lygodesmia aphylla Rugel's pawpaw Deeringothamnus rugelii Hempweed Mikania cordifolia White Topped Aster Oclemena reticulata Apiaceae Goldenaster Pityopsis graminifolia Button Rattlesnake Master Eryngium yuccifolium Rosy Camphorweed Pluchea rosea Dollarweed Hydrocotyle sp. Pluchea Pluchea spp. Mock Bishopweed Ptilimnium capillaceum Rabbit Tobacco Pseudognaphalium obtusifolium Blackroot Pterocaulon virgatum -
Bromeliads Bromeliads Are a Family of Plants (Bromeliaceae, the Pineapple Family) Native to Tropical North and South America
A Horticulture Information article from the Wisconsin Master Gardener website, posted 19 March 2012 Bromeliads Bromeliads are a family of plants (Bromeliaceae, the pineapple family) native to tropical North and South America. Europeans fi rst found out about bromeliads on Columbus’ second trip to the New World in 1493, where the pineapple (Ananas sp.) was being cultivated by the Carib tribe in the West Indies. The commercial pineapple (Ananas comosus) is native to southern Brazil and Paraguay. After the colonization of the New World it was rapidly transported to all areas of the tropics, and now is widely grown in tropical and sub- tropical areas. The only A collection of bromeliads placed on a tree at Costa Flores, Costa Rica. bromeliad to occur north of the tropics is Spanish “moss” (Tillandsia usneoides). It is neither Spanish nor a moss, but an epiphytic bromeliad. It doesn’t look much like a typical Commercial pineapple, Ananas comosus, bromeliad, though, with its long scaly stems and reduced in the fi eld. fl owers. Bromeliads are monocots, many of which, like their grass relatives, have a special form of photosynthesis that uses a variation of the more usual biochemical pathways to allow them to use water more effi ciently. Even though they come from the tropics, this helps those that are epiphytes contend with life in the treetops where there is limited water and a real danger of drying out. There are about 2500 species Many bromeliads are tropical and several thousand hybrids epiphytes. and cultivars. Many have brightly colored leaves, fl owers or fruit, and range in size from moss-like species of Tillandsia to the enormous Puya raimondii from the Andes which produces a fl owering stem up to 15 feet tall. -
Floristic Discoveries in Delaware, Maryland, and Virginia
Knapp, W.M., R.F.C. Naczi, W.D. Longbottom, C.A. Davis, W.A. McAvoy, C.T. Frye, J.W. Harrison, and P. Stango, III. 2011. Floristic discoveries in Delaware, Maryland, and Virginia. Phytoneuron 2011-64: 1–26. Published 15 December 2011. ISSN 2153 733X FLORISTIC DISCOVERIES IN DELAWARE, MARYLAND, AND VIRGINIA WESLEY M. KNAPP 1 Maryland Department of Natural Resources Wildlife and Heritage Service Wye Mills, Maryland 21679 [email protected] ROBERT F. C. NACZI The New York Botanical Garden Bronx, New York 10458-5126 WAYNE D. LONGBOTTOM P.O. Box 634 Preston, Maryland 21655 CHARLES A. DAVIS 1510 Bellona Ave. Lutherville, Maryland 21093 WILLIAM A. MCAVOY Delaware Natural Heritage and Endangered Species Program 4876 Hay Point, Landing Rd. Smyrna, Delaware 19977 CHRISTOPHER T. FRYE Maryland Department of Natural Resources Wildlife and Heritage Service Wye Mills, Maryland 21679 JASON W. HARRISON Maryland Department of Natural Resources Wildlife and Heritage Service Wye Mills, Maryland 21679 PETER STANGO III Maryland Department of Natural Resources, Wildlife and Heritage Service, Annapolis, Maryland 21401 1 Author for correspondence ABSTRACT Over the past decade studies in the field and herbaria have yielded significant advancements in the knowledge of the floras of Delaware, Maryland, and the Eastern Shore of Virginia. We here discuss fifty-two species newly discovered or rediscovered or whose range or nativity is clarified. Eighteen are additions to the flora of Delaware ( Carex lucorum var. lucorum, Carex oklahomensis, Cyperus difformis, Cyperus flavicomus, Elymus macgregorii, Glossostigma cleistanthum, Houstonia pusilla, Juncus validus var. validus, Lotus tenuis, Melothria pendula var. pendula, Parapholis incurva, Phyllanthus caroliniensis subsp. -
Physiological, Anatomical, and Ecological Characteristics of Southern Live Oak
PHYSIOLOGICAL, ANATOMICAL, AND ECOLOGICAL CHARACTERISTICS OF SOUTHERN LIVE OAK Yadong Qi, Jammie Favorite, Kit L. Chin, and Ying Xiao1 Abstract—Gas exchanges of sun-exposed and shaded leaves of southern live oak (Quercus virginiana Mill.) were studied monthly from May to September, 2000. Six healthy live oak trees with d.b.h. ranging from 21 to 148 cm on Southern University’s campus in Baton Rouge, LA, were selected for the study. Instantaneous gas exchanges were measured during clear sky days from 9 a.m. to 4 p.m. using a portable gas exchange system. Leaf chlorophyll, moisture content, and environ- mental conditions were also monitored. Anatomy of sun-exposed and shaded leaves was studied in July using a scanning electron microscopy. Sun-exposed leaves had significantly higher net carbon dioxide (CO2) uptake rate, transpiration rate, and chlorophyll content, and significantly lower internal CO2 concentration and moisture content than the shaded leaves. The leaf anatomy related well to the leaf physiology. The sun-exposed leaves had a remarkably denser trichome layer and more closely packed palisade mesophyll cells than the shaded leaves. The combined leaf anatomy and physiology indicate that southern live oak possesses a unique ecological advantage of self defense against various environmental stresses. INTRODUCTION Increasing levels of atmospheric CO2 and other greenhouse Southern live oak (Quercus virginiana, Mill.) is predominately gases are thought by many to be leading to increased atmo- a landscape and shade tree species that is considered a spheric temperatures (Nowak 1994a). Trees act as a sink for virtual emblem of the Old South. Live oak is a picturesque atmospheric CO2 by storing carbon (C) through their growth native tree found in the lower coastal plain of the Southeastern processes. -
Tillandsia Recurvata Is the Most Wide
ZLATKO JANEBA Tillandsia recurvata illandsia recurvata is the most wide- even known to grow on roofs and power lines. spread bromeliad. It occurs in the T. recurvata is the type species of subgenus Dia- southern US, where it stretches phoranthema, which contains some 30 variable and from Florida all the way to Arizo- mostly miniature species that have small, incon- na, and as far south as as Argenti- spicuous flowers. Members of Diaphoranthema are na and Chile. It grows epiphytical- common and locally abundant in South Ameri- ly on trees, bushes, and cacti or as ca, with a distribution centered in Argentina and a petrophyte on rocky cliffs. It is Bolivia. Only two species reach North America: T. recurvata (aka Small Ballmoss) was found growing close to the ground on the side of the barrel cactus Echinocactus platyacanthus near La Ascención, Nuevo León, Mexico (right). More often, T. recurvata is spotted (right) clinging to the bark of pine trees (Pinus johannis and Pinus arizonica var stormiae), as seen here at a Tspot between Santa Lucia and El Pinito, Nuevo León. 2 CACTUS AND SUCCULENT JOURNAL T. recurvata, sometimes called Small Ballmoss, and Tillandsia species, such as T. capillaris, T. croca- T. usneoides, the well known Spanish Moss. ta, and T. mallemontii, which are found in simi- Polyploidy, the condition wherein a plant con- lar habitats but which have different flower char- tains more than one set of chromosomes in its acteristics. cells, is common in this subgenus. Normally we T. recurvata was described by Carl Linnaeus think of polyploidy resulting in larger-than-nor- as Renealmia recurvata in 1753, the same year mal plants, but these bromeliads tend to be quite that he erected the genus Tillandsia. -
Water Relations of Bromeliaceae in Their Evolutionary Context
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Apollo Botanical Journal of the Linnean Society, 2016, 181, 415–440. With 2 figures Think tank: water relations of Bromeliaceae in their evolutionary context JAMIE MALES* Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EA, UK Received 31 July 2015; revised 28 February 2016; accepted for publication 1 March 2016 Water relations represent a pivotal nexus in plant biology due to the multiplicity of functions affected by water status. Hydraulic properties of plant parts are therefore likely to be relevant to evolutionary trends in many taxa. Bromeliaceae encompass a wealth of morphological, physiological and ecological variations and the geographical and bioclimatic range of the family is also extensive. The diversification of bromeliad lineages is known to be correlated with the origins of a suite of key innovations, many of which relate directly or indirectly to water relations. However, little information is known regarding the role of change in morphoanatomical and hydraulic traits in the evolutionary origins of the classical ecophysiological functional types in Bromeliaceae or how this role relates to the diversification of specific lineages. In this paper, I present a synthesis of the current knowledge on bromeliad water relations and a qualitative model of the evolution of relevant traits in the context of the functional types. I use this model to introduce a manifesto for a new research programme on the integrative biology and evolution of bromeliad water-use strategies. The need for a wide-ranging survey of morphoanatomical and hydraulic traits across Bromeliaceae is stressed, as this would provide extensive insight into structure– function relationships of relevance to the evolutionary history of bromeliads and, more generally, to the evolutionary physiology of flowering plants. -
Key to Leaves of Eastern Native Oaks
FHTET-2003-01 January 2003 Front Cover: Clockwise from top left: white oak (Q. alba) acorns; willow oak (Q. phellos) leaves and acorns; Georgia oak (Q. georgiana) leaf; chinkapin oak (Q. muehlenbergii) acorns; scarlet oak (Q. coccinea) leaf; Texas live oak (Q. fusiformis) acorns; runner oak (Q. pumila) leaves and acorns; background bur oak (Q. macrocarpa) bark. (Design, D. Binion) Back Cover: Swamp chestnut oak (Q. michauxii) leaves and acorns. (Design, D. Binion) FOREST HEALTH TECHNOLOGY ENTERPRISE TEAM TECHNOLOGY TRANSFER Oak Identification Field Guide to Native Oak Species of Eastern North America John Stein and Denise Binion Forest Health Technology Enterprise Team USDA Forest Service 180 Canfield St., Morgantown, WV 26505 Robert Acciavatti Forest Health Protection Northeastern Area State and Private Forestry USDA Forest Service 180 Canfield St., Morgantown, WV 26505 United States Forest FHTET-2003-01 Department of Service January 2003 Agriculture NORTH AMERICA 100th Meridian ii iii ACKNOWLEDGMENTS The authors wish to thank all those who helped with this publication. We are grateful for permission to use the drawings illustrated by John K. Myers, Flagstaff, AZ, published in the Flora of North America, North of Mexico, vol. 3 (Jensen 1997). We thank Drs. Cynthia Huebner and Jim Colbert, U.S. Forest Service, Northeastern Research Station, Disturbance Ecology and Management of Oak-Dominated Forests, Morgantown, WV; Dr. Martin MacKenzie, U.S. Forest Service, Northeastern Area State and Private Forestry, Forest Health Protection, Morgantown, WV; Dr. Steven L. Stephenson, Department of Biology, Fairmont State College, Fairmont, WV; Dr. Donna Ford-Werntz, Eberly College of Arts and Sciences, West Virginia University, Morgantown, WV; Dr.