6. QUERCUS Linnaeus, Sp. Pl. 2: 994. 1753. 栎属 Li Shu Trees Or Sometimes Shrubs, Evergreen Or Deciduous
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Department of Planning and Zoning
Department of Planning and Zoning Subject: Howard County Landscape Manual Updates: Recommended Street Tree List (Appendix B) and Recommended Plant List (Appendix C) - Effective July 1, 2010 To: DLD Review Staff Homebuilders Committee From: Kent Sheubrooks, Acting Chief Division of Land Development Date: July 1, 2010 Purpose: The purpose of this policy memorandum is to update the Recommended Plant Lists presently contained in the Landscape Manual. The plant lists were created for the first edition of the Manual in 1993 before information was available about invasive qualities of certain recommended plants contained in those lists (Norway Maple, Bradford Pear, etc.). Additionally, diseases and pests have made some other plants undesirable (Ash, Austrian Pine, etc.). The Howard County General Plan 2000 and subsequent environmental and community planning publications such as the Route 1 and Route 40 Manuals and the Green Neighborhood Design Guidelines have promoted the desirability of using native plants in landscape plantings. Therefore, this policy seeks to update the Recommended Plant Lists by identifying invasive plant species and disease or pest ridden plants for their removal and prohibition from further planting in Howard County and to add other available native plants which have desirable characteristics for street tree or general landscape use for inclusion on the Recommended Plant Lists. Please note that a comprehensive review of the street tree and landscape tree lists were conducted for the purpose of this update, however, only -
Sawtooth Oak Planting Guide
Planting Guide and into southern New England (USDA plant hardiness zones 5b through 8b). On exposed sites in SAWTOOH OAK the northern Finger Lakes Region of New York, it may winterkill. Sawtooth oak is winter hardy and Quercus acutissima can be grown in droughty and well-drained soils from Carruthers sandy loam to clay loam. However, the best performance is achieved in deep, well-drained soils. plant symbol = QUAC80 It can also be grown on reclaimed surface mined land where favorable moisture conditions are present and pH is above 5.0. For a current distribution map, please consult the Plant Profile page for this species on the PLANTS Website. Establishment Sawtooth oak may be established, from bareroot seedlings, containerized plants, or acorns. One year old bareroot seedlings or containerized plants should be planted 15-20 feet apart for maximum acorn production. In areas where multiple rows are used, the spacing should be no less than 20 feet apart. In seed orchards, there should be at least 15 plants per C. Miller USDA NRCS planting for effective wind pollination. Uses Bareroot seedlings must be planted while the plants The primary use for this species is as a wildlife food are dormant (from the average date of first frost in source and cover. It is also a good shade tree. the fall until the average date of last frost in the spring). Containerized plants may be planted later in the spring, but may require frequent irrigation to Status survive. Please consult the PLANTS Web site and your State Department of Natural Resources for this plant’s Sites for landscape plantings and seed orchards current status (e.g. -
Soil Seed Burial and Competition with Surrounding Plants Determine the Emergence and Development of Seedling of an Endangered Species Horsfeldia Hainanensis Merr
www.nature.com/scientificreports OPEN Soil seed burial and competition with surrounding plants determine the emergence and development of seedling of an endangered species Horsfeldia hainanensis Merr. in China Xiongsheng Liu1, Yinghui He1, Yufei Xiao1, Yong Wang1, Yinghong Jiang2 & Yi Jiang1* Three well-conserved Horsfeldia hainanensis Merr. populations were used to investigate their soil seed bank and seedling regeneration characteristics and their relationship to environmental factors. The results showed that the seed reserves were low in the H. hainanensis soil seed bank (16.93~24.74 seed/m2). The distribution pattern for the seeds and seedlings in the H. hainanensis populations was aggregated, and they were mainly found around 2–3 m from the mother plant. The seeds in the litter layer and the 5–10 cm soil layer showed no vigor, and only 25.7%~33.3% of the total seeds in the 0–5 cm soil layer were viable afected by the high temperature and humidity, the animals’ eating and poisoning. Afected by the height and coverage of the surrounding herbaceous layer and shrub layer, the seedlings of H. hainanensis could not obtain enough light and nutrients in the competition, resulting in the survival competitiveness of 1- to 3-year-old (1–3a) seedlings in the habitat had been in a weak position and a large number of seedlings died. It would take at least four years for seedlings to develop under the current environmental constraints. It can be concluded that the low seed reserve in the soil seed bank and high mortality of seedlings of H. hainanensis lead to slow or even stagnation of population regeneration, which was an important reason for the endangered of H. -
Qrno. 1 2 3 4 5 6 7 1 CP 2903 77 100 0 Cfcl3
QRNo. General description of Type of Tariff line code(s) affected, based on Detailed Product Description WTO Justification (e.g. National legal basis and entry into Administration, modification of previously the restriction restriction HS(2012) Article XX(g) of the GATT, etc.) force (i.e. Law, regulation or notified measures, and other comments (Symbol in and Grounds for Restriction, administrative decision) Annex 2 of e.g., Other International the Decision) Commitments (e.g. Montreal Protocol, CITES, etc) 12 3 4 5 6 7 1 Prohibition to CP 2903 77 100 0 CFCl3 (CFC-11) Trichlorofluoromethane Article XX(h) GATT Board of Eurasian Economic Import/export of these ozone destroying import/export ozone CP-X Commission substances from/to the customs territory of the destroying substances 2903 77 200 0 CF2Cl2 (CFC-12) Dichlorodifluoromethane Article 46 of the EAEU Treaty DECISION on August 16, 2012 N Eurasian Economic Union is permitted only in (excluding goods in dated 29 may 2014 and paragraphs 134 the following cases: transit) (all EAEU 2903 77 300 0 C2F3Cl3 (CFC-113) 1,1,2- 4 and 37 of the Protocol on non- On legal acts in the field of non- _to be used solely as a raw material for the countries) Trichlorotrifluoroethane tariff regulation measures against tariff regulation (as last amended at 2 production of other chemicals; third countries Annex No. 7 to the June 2016) EAEU of 29 May 2014 Annex 1 to the Decision N 134 dated 16 August 2012 Unit list of goods subject to prohibitions or restrictions on import or export by countries- members of the -
New York City Approved Street Trees
New York City Approved Street Trees Suggested Tree Species Shape Visual interest Frequency of Preferred Cultivars Notes Scientific Name Common Name Planting Acer rubrum Red Maple Sparingly 'Red Sunset' ALB Host Aesculus hippocastanum Horsechestnut White May flowers Sparingly 'Baumanni' ALB Host Aesculus octandra Yellow Buckeye Yellow May Flowers Sparingly ALB Host ALB Host 'Duraheat' Betula nigra River Birch Ornamental Bark Sparingly Plant Single Stem 'Heritage' Only Celtis occidentalis Hackberry Ornamental Bark Sparingly 'Magnifica' ALB Host ALB Host Cercidiphyllum japonicum Katsura Tree Sparingly Plant Single Stem Only Corylus colurna Turkish Filbert Sparingly LARGE TREES: Mature LARGE TREES: height than greater feet 50 tall Eucommia ulmoides Hardy Rubber Tree Frequently 'Asplenifolia' Fagus sylvatica European Beech Sparingly 'Dawyckii Purple' 'Autumn Gold' Ginkgo biloba Ginkgo Yellow Fall Color Moderately 'Magyar' Very Tough Tree 'Princeton Sentry' 'Shademaster' 'Halka' Gleditsia triacanthos var inermis Honeylocust Yellow Fall Color Moderately 'Imperial' 'Skyline' 'Espresso' Gymnocladus dioicus Kentucky Coffeetree Large Tropical Leaves Frequently 'Prairie Titan' Page 1 of 7 New York City Approved Street Trees Suggested Tree Species Shape Visual interest Frequency of Preferred Cultivars Notes Scientific Name Common Name Planting 'Rotundiloba' Seedless Cultivars Liquidambar styraciflua Sweetgum Excellent Fall Color Frequently 'Worplesdon' Preffered 'Cherokee' Orange/Green June Liriodendron tulipifera Tulip Tree Moderately Flowers Metasequoia -
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. -
Complete Chloroplast Genome Sequence and Phylogenetic Analysis of Quercus Bawanglingensis Huang, Li Et Xing, a Vulnerable Oak Tree in China
Article Complete Chloroplast Genome Sequence and Phylogenetic Analysis of Quercus bawanglingensis Huang, Li et Xing, a Vulnerable Oak Tree in China Xue Liu 1 , Er-Mei Chang 1, Jian-Feng Liu 1,* , Yue-Ning Huang 1, Ya Wang 1, Ning Yao 1 and Ze-Ping Jiang 1,2 1 Key Laboratory of Tree Breeding and Cultivation of State Forestry Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 100091, China 2 Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Beijing 100091, China * Correspondence: [email protected] Received: 5 June 2019; Accepted: 12 July 2019; Published: 15 July 2019 Abstract: Quercus bawanglingensis Huang, Li et Xing, an endemic evergreen oak of the genus Quercus (Fagaceae) in China, is currently listed in the Red List of Chinese Plants as a vulnerable (VU) plant. No chloroplast (cp) genome information is currently available for Q. bawanglingensis, which would be essential for the establishment of guidelines for its conservation and breeding. In the present study, the cp genome of Q. bawanglingensis was sequenced and assembled into double-stranded circular DNA with a length of 161,394 bp. Two inverted repeats (IRs) with a total of 51,730 bp were identified, and the rest of the sequence was separated into two single-copy regions, namely, a large single-copy (LSC) region (90,628 bp) and a small single-copy (SSC) region (19,036 bp). The genome of Q. bawanglingensis contains 134 genes (86 protein-coding genes, 40 tRNAs and eight rRNAs). More forward (29) than inverted long repeats (21) are distributed in the cp genome. -
Quercus ×Coutinhoi Samp. Discovered in Australia Charlie Buttigieg
XXX International Oaks The Journal of the International Oak Society …the hybrid oak that time forgot, oak-rod baskets, pros and cons of grafting… Issue No. 25/ 2014 / ISSN 1941-2061 1 International Oaks The Journal of the International Oak Society … the hybrid oak that time forgot, oak-rod baskets, pros and cons of grafting… Issue No. 25/ 2014 / ISSN 1941-2061 International Oak Society Officers and Board of Directors 2012-2015 Officers President Béatrice Chassé (France) Vice-President Charles Snyers d’Attenhoven (Belgium) Secretary Gert Fortgens (The Netherlands) Treasurer James E. Hitz (USA) Board of Directors Editorial Committee Membership Director Chairman Emily Griswold (USA) Béatrice Chassé Tour Director Members Shaun Haddock (France) Roderick Cameron International Oaks Allen Coombes Editor Béatrice Chassé Shaun Haddock Co-Editor Allen Coombes (Mexico) Eike Jablonski (Luxemburg) Oak News & Notes Ryan Russell Editor Ryan Russell (USA) Charles Snyers d’Attenhoven International Editor Roderick Cameron (Uruguay) Website Administrator Charles Snyers d’Attenhoven For contributions to International Oaks contact Béatrice Chassé [email protected] or [email protected] 0033553621353 Les Pouyouleix 24800 St.-Jory-de-Chalais France Author’s guidelines for submissions can be found at http://www.internationaloaksociety.org/content/author-guidelines-journal-ios © 2014 International Oak Society Text, figures, and photographs © of individual authors and photographers. Graphic design: Marie-Paule Thuaud / www.lecentrecreatifducoin.com Photos. Cover: Charles Snyers d’Attenhoven (Quercus macrocalyx Hickel & A. Camus); p. 6: Charles Snyers d’Attenhoven (Q. oxyodon Miq.); p. 7: Béatrice Chassé (Q. acerifolia (E.J. Palmer) Stoynoff & W. J. Hess); p. 9: Eike Jablonski (Q. ithaburensis subsp. -
Light Spectra Modify Nitrogen Assimilation and Nitrogen
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.02.407924; this version posted December 2, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Light spectra modify nitrogen assimilation and nitrogen 2 content in Quercus variabilis Blume seedling components: 3 A bioassay with 15N pulses 4 Jun Gao 1,2, Jinsong Zhang 1,2, Chunxia He 1,2,*, Qirui Wang 3 5 1 Key Laboratory of Tree Breeding and Cultivation of State Forestry Administration, Research Institute of Forestry, 6 Chinese Academy of Forestry, Beijing 100091, China; [email protected]; [email protected]; [email protected] 7 2 Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China 8 3 Henan Academy of Forestry, Zhengzhou 450008, China; [email protected] 9 10 * Correspondence: Dr. Chunxia He, email: [email protected], address: Key Laboratory of Tree Breeding and 11 Cultivation, State Forestry Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 12 100091, China; Fax & phone: +86-10-6288-9668 13 bioRxiv preprint doi: https://doi.org/10.1101/2020.12.02.407924; this version posted December 2, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. -
Chapter 4 Phytogeography of Northeast Asia
Chapter 4 Phytogeography of Northeast Asia Hong QIAN 1, Pavel KRESTOV 2, Pei-Yun FU 3, Qing-Li WANG 3, Jong-Suk SONG 4 and Christine CHOURMOUZIS 5 1 Research and Collections Center, Illinois State Museum, 1011 East Ash Street, Springfield, IL 62703, USA, e-mail: [email protected]; 2 Institute of Biology and Soil Science, Russian Academy of Sciences, Vladivostok, 690022, Russia, e-mail: [email protected]; 3 Institute of Applied Ecology, Chinese Academy of Sciences, P.O. Box 417, Shenyang 110015, China; 4 Department of Biological Science, College of Natural Sciences, Andong National University, Andong 760-749, Korea, e-mail: [email protected]; 5 Department of Forest Sciences, University of British Columbia, 3041-2424 mail Mall, Vancouver, B.C., V6T 1Z4, Canada, e-mail: [email protected] Abstract: Northeast Asia as defined in this study includes the Russian Far East, Northeast China, the northern part of the Korean Peninsula, and Hokkaido Island (Japan). We determined the species richness of Northeast Asia at various spatial scales, analyzed the floristic relationships among geographic regions within Northeast Asia, and compared the flora of Northeast Asia with surrounding floras. The flora of Northeast Asia consists of 971 genera and 4953 species of native vascular plants. Based on their worldwide distributions, the 971 gen- era were grouped into fourteen phytogeographic elements. Over 900 species of vascular plants are endemic to Northeast Asia. Northeast Asia shares 39% of its species with eastern Siberia-Mongolia, 24% with Europe, 16.2% with western North America, and 12.4% with eastern North America. -
Genetic Diversity and Structure of Natural Quercus Variabilis Population in China As Revealed by Microsatellites Markers
Article Genetic Diversity and Structure of Natural Quercus variabilis Population in China as Revealed by Microsatellites Markers Xiaomeng Shi 1,†, Qiang Wen 2,†, Mu Cao 1, Xin Guo 1 and Li-an Xu 1,* 1 Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China; [email protected] (X.S.); [email protected] (M.C.); [email protected] (X.G.) 2 Plant Bio-tech Key Laboratory of Jiangxi Province, Jiangxi Academy of Forestry, Nanchang 330013, China; [email protected] * Correspondence: [email protected]; Tel.: +86-025-8542-7882 † These two authors contribute equally to this work. Received: 3 November 2017; Accepted: 7 December 2017; Published: 11 December 2017 Abstract: Quercus variabilis is a tree species of ecological and economic value that is widely distributed in China. To effectively evaluate, use, and conserve resources, we applied 25 pairs of simple sequence repeat (SSR) primers to study its genetic diversity and genetic structure in 19 natural forest or natural secondary forest populations of Q. variabilis (a total of 879 samples). A total of 277 alleles were detected. Overall, the average expected heterozygosity (He) was 0.707 and average allelic richness (AR) was 7.79. Q. variabilis manifested a loss of heterozygosity, and the mean of inbreeding coefficient (FIS) was 0.044. Less differentiation among populations was observed, and the genetic differentiation coefficient (FST) was 0.063. Bayesian clustering analysis indicated that the 19 studied populations could be divided into three groups based on their genetic makeup, namely, the Southwest group, Central group, and Northeastern group. The Central group, compared to the populations of the Southwest and Northeast group, showed higher genetic diversities and lower genetic differentiations.