Redwood | Sequoia Sempervirens
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Thuja Plicata Has Many Traditional Uses, from the Manufacture of Rope to Waterproof Hats, Nappies and Other Kinds of Clothing
photograph © Daniel Mosquin Culturally modified tree. The bark of Thuja plicata has many traditional uses, from the manufacture of rope to waterproof hats, nappies and other kinds of clothing. Careful, modest, bark stripping has little effect on the health or longevity of trees. (see pages 24 to 35) photograph © Douglas Justice 24 Tree of the Year : Thuja plicata Donn ex D. Don In this year’s Tree of the Year article DOUGLAS JUSTICE writes an account of the western red-cedar or giant arborvitae (tree of life), a species of conifers that, for centuries has been central to the lives of people of the Northwest Coast of America. “In a small clearing in the forest, a young woman is in labour. Two women companions urge her to pull hard on the cedar bark rope tied to a nearby tree. The baby, born onto a newly made cedar bark mat, cries its arrival into the Northwest Coast world. Its cradle of firmly woven cedar root, with a mattress and covering of soft-shredded cedar bark, is ready. The young woman’s husband and his uncle are on the sea in a canoe carved from a single red-cedar log and are using paddles made from knot-free yellow cedar. When they reach the fishing ground that belongs to their family, the men set out a net of cedar bark twine weighted along one edge by stones lashed to it with strong, flexible cedar withes. Cedar wood floats support the net’s upper edge. Wearing a cedar bark hat, cape and skirt to protect her from the rain and INTERNATIONAL DENDROLOGY SOCIETY TREES Opposite, A grove of 80- to 100-year-old Thuja plicata in Queen Elizabeth Park, Vancouver. -
Growth and Colonization of Western Redcedar by Vesicular-Arbuscular Mycorrhizae in Fumigated and Nonfumigated Nursery Beds
Tree Planter's Notes, Volume 42, No. 4 (1991) Growth and Colonization of Western Redcedar by Vesicular-Arbuscular Mycorrhizae in Fumigated and Nonfumigated Nursery Beds S. M. Berch, E. Deom, and T. Willingdon Assistant professor and research assistant, Department of Soil Science, University of British Columbia, Vancouver, BC, and manager, Surrey Nursery, British Columbia Ministry of Forests, Surrey, BC Western redcedar (Thuja plicata Donn ex D. Don) VAM. Positive growth responses of up to 20 times the seedlings were grown in a bareroot nursery bed that had nonmycorrhizal controls occurred under conditions of limited been fumigated with methyl bromide. Seedlings grown in soil phosphorus. Incense-cedar, redwood, and giant sequoia fumigated beds were stunted and had purple foliage. seedlings in northern California nursery beds are routinely Microscopic examination showed that roots from these inoculated with Glomus sp. (Adams et al. 1990), as seedlings were poorly colonized by mycorrhizae, and only by experience has shown that the absence of VAM after soil fine vesicular-arbuscular mycorrhizae. In contrast, roots from fumigation leads to phosphorus deficiency and poor growth. seedlings grown in non-fumigated beds had larger shoots and When western redcedars in fumigated transplant beds at green foliage and were highly colonized by both fine and the British Columbia Ministry of Forest's Surrey Nursery coarse vesicular-arbuscular mycorrhizae. Tree Planters' began to show signs of phosphorus deficiency, a deficiency Notes 42(4):14-16; 1991. of mycorrhizal colonization was suspected. Many studies have demonstrated improved P status of VAM-inoculated Species of cypress (Cupressaceae) and yew plants (see Harley and Smith 1983). -
Metasequoia Dawn Redwood a Truly Beautiful Tree
Metasequoia Dawn Redwood A Truly Beautiful Tree Metasequoia glyptostroboides is considered to be a living fossil as it is the only remaining species of a genus that was widespread in the geological past. In 1941 it was discovered in Hubei, China. In 1948 the Arnold Arboretum of Harvard University sent an expedition to collect seed, which was distributed to universities and botanical gardens worldwide for growth trials. Seedlings were raised in New Zealand and trees can be seen in Christchurch Botanical Gardens, Eastwoodhill and Queens Gardens, Nelson. A number of natural Metasequoia populations exist in the wetlands and valleys of Lichuan County, Hubei, mostly as small groups. The largest contains 5400 trees. It is an excellent tall growing deciduous tree to complement evergreens in wetlands, stream edge plantings to control slips, and to prevent erosion in damp valley bottoms where other forestry trees fail to grow. Spring growth is a fresh bright green and in autumn the foliage turns a A fast growing deciduous conifer, red coppery brown making a great display. with a straight trunk, numerous It is also a most attractive winter branch silhouette. While the foliage is a similiar colour in autumn to that of swamp cypress (Taxodium), it is a branches and a tall conical crown, much taller erect growing tree, though both species thrive in moist soil growing to 45 metres in height and conditions. We import our seed from China and the uniformity of the seedling one metre in diameter. crop is most impressive. The timber has been used in boat building. Abies vejari 20 years old on left 14 years old on right Abies Silver Firs These dramatic conical shaped conifers make a great statement in the landscape, long-lived and withstanding the elements. -
Cupressaceae Calocedrus Decurrens Incense Cedar
Cupressaceae Calocedrus decurrens incense cedar Sight ID characteristics • scale leaves lustrous, decurrent, much longer than wide • laterals nearly enclosing facials • seed cone with 3 pairs of scale/bract and one central 11 NOTES AND SKETCHES 12 Cupressaceae Chamaecyparis lawsoniana Port Orford cedar Sight ID characteristics • scale leaves with glaucous bloom • tips of laterals on older stems diverging from branch (not always too obvious) • prominent white “x” pattern on underside of branchlets • globose seed cones with 6-8 peltate cone scales – no boss on apophysis 13 NOTES AND SKETCHES 14 Cupressaceae Chamaecyparis thyoides Atlantic white cedar Sight ID characteristics • branchlets slender, irregularly arranged (not in flattened sprays). • scale leaves blue-green with white margins, glandular on back • laterals with pointed, spreading tips, facials closely appressed • bark fibrous, ash-gray • globose seed cones 1/4, 4-5 scales, apophysis armed with central boss, blue/purple and glaucous when young, maturing in fall to red-brown 15 NOTES AND SKETCHES 16 Cupressaceae Callitropsis nootkatensis Alaska yellow cedar Sight ID characteristics • branchlets very droopy • scale leaves more or less glabrous – little glaucescence • globose seed cones with 6-8 peltate cone scales – prominent boss on apophysis • tips of laterals tightly appressed to stem (mostly) – even on older foliage (not always the best character!) 15 NOTES AND SKETCHES 16 Cupressaceae Taxodium distichum bald cypress Sight ID characteristics • buttressed trunks and knees • leaves -
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). -
Plant Palette - Trees 50’-0”
50’-0” 40’-0” 30’-0” 20’-0” 10’-0” Zelkova Serrata “Greenvase” Metasequoia glyptostroboides Cladrastis kentukea Chamaecyparis obtusa ‘Gracilis’ Ulmus parvifolia “Emer I” Green Vase Zelkova Dawn Redwood American Yellowwood Slender Hinoki Falsecypress Athena Classic Elm • Vase shape with upright arching branches • Narrow, conical shape • Horizontally layered, spreading form • Narrow conical shape • Broadly rounded, pendulous branches • Green foliage • Medium green, deciduous conifer foliage • Dark green foliage • Evergreen, light green foliage • Medium green, toothed leaves • Orange Fall foliage • Rusty orange Fall foliage • Orange to red Fall foliage • Evergreen, no Fall foliage change • Yellowish fall foliage Plant Palette - Trees 50’-0” 40’-0” 30’-0” 20’-0” 10’-0” Quercus coccinea Acer freemanii Cercidiphyllum japonicum Taxodium distichum Thuja plicata Scarlet Oak Autumn Blaze Maple Katsura Tree Bald Cyprus Western Red Cedar • Pyramidal, horizontal branches • Upright, broad oval shape • Pyramidal shape • Pyramidal shape, develops large flares at base • Pyramidal, buttressed base with lower branches • Long glossy green leaves • Medium green fall foliage • Bluish-green, heart-shaped foliage • Leaves are needle-like, green • Leaves green and scale-like • Scarlet red Fall foliage • Brilliant orange-red, long lasting Fall foliage • Soft apricot Fall foliage • Rich brown Fall foliage • Sharp-pointed cone scales Plant Palette - Trees 50’-0” 40’-0” 30’-0” 20’-0” 10’-0” Thuja plicata “Fastigiata” Sequoia sempervirens Davidia involucrata Hogan -
The Pine Genome Initiative- Science Plan Review
ProCoGen Training Workshop 2013 Umeå An Undiscovered Country: What Comparative Genomics Tells Us of Gymnosperm Genomes Ujwal R. Bagal, W. Walter Lorenz, Jeffrey F.D. Dean Warnell School of Forestry and Natural Resources & Institute of Bioinformatics University of Georgia Diverse Form and Life History JGI CSP - Conifer EST Project Transcriptome Assemblies Statistics Pinaceae Reads Contigs* • Pinus taeda 4,074,360 164,506 • Pinus palustris 542,503 44,975 • Pinus lambertiana 1,096,017 85,348 • Picea abies 623,144 36,867 • Cedrus atlantica 408,743 30,197 • Pseudotsuga menziesii 1,216,156 60,504 Other Conifer Families • Wollemia nobilis 471,719 35,814 • Cephalotaxus harringtonia 689,984 40,884 • Sequoia sempervirens 472,601 42,892 • Podocarpus macrophylla 584,579 36,624 • Sciadopitys verticillata 479,239 29,149 • Taxus baccata 398,037 33,142 *Assembled using MIRA http://ancangio.uga.edu/ng-genediscovery/conifer_dbMagic.jnlp Loblolly pine PAL amino acid sequence alignment Analysis Method Sequence Collection PlantTribe, PlantGDB, GenBank, Conifer DBMagic assemblies 25 taxa comprising of 71 sequences Phylogenetic analysis Maximum Likelihood: RAxML (Stamatakis et. al) Bayesian Method: MrBayes (Huelsenbeck, et al.) Tree reconciliation: NOTUNG 2.6 (Chen et al.) Phylogenetic Tree of Vascular Plant PALs Phylogenetic Analysis of Conifer PAL Gene Sequences Conifer-specific branch shown in green Amino Acids Under Relaxed Constraint Maximum Likelihood analysis Nested codon substitution models M0 : constant dN/dS ratio M2a : rate ratio ω1< 1, ω2=1 and ω3>1 M3 : (ω1< ω2< ω3) (M0, M2a, M3, M2a+S1, M2a+S2, M3+S1, M3+S2) Fitmodel version 0.5.3 ( Guindon et al. 2004) S1 : equal switching rates (alpha =beta) S2 : unequal switching rates (alpha ≠ beta) Variable gymnosperm PAL amino acid residues mapped onto a crystal structure for parsley PAL Ancestral polyploidy in seed plants and angiosperms Jiao et al. -
Aneides Vagrans Residing in the Canopy of Old-Growth Redwood Forest 1 1 1 James C
Herpetological Conservation and Biology 1(1):16-26 Submitted: June 15, 2006; Accepted: July 19, 2006 EVIDENCE OF A NEW NICHE FOR A NORTH AMERICAN SALAMANDER: ANEIDES VAGRANS RESIDING IN THE CANOPY OF OLD-GROWTH REDWOOD FOREST 1 1 1 JAMES C. SPICKLER , STEPHEN C. SILLETT , SHARYN B. MARKS , 2,3 AND HARTWELL H. WELSH, JR. 1Department of Biological Sciences, Humboldt State University, Arcata, CA 95521, USA 2Redwood Sciences Laboratory, USDA Forest Service, 1700 Bayview Drive, Arcata, CA 95521, USA 3Corresponding Author, email: [email protected] Abstract.—We investigated habitat use and movements of the wandering salamander, Aneides vagrans, in an old-growth forest canopy. We conducted a mark-recapture study of salamanders in the crowns of five large redwoods (Sequoia sempervirens) in Prairie Creek Redwoods State Park, California. This represented a first attempt to document the residency and behavior of A. vagrans in a canopy environment. We placed litter bags on 65 fern (Polypodium scouleri) mats, covering 10% of their total surface area in each tree. Also, we set cover boards on one fern mat in each of two trees. We checked cover objects 2–4 times per month during fall and winter seasons. We marked 40 individuals with elastomer tags and recaptured 13. Only one recaptured salamander moved (vertically 7 m) from its original point of capture. We compared habitats associated with salamander captures using correlation analysis and stepwise regression. At the tree-level, the best predictor of salamander abundance was water storage by fern mats. At the fern mat-level, the presence of cover boards accounted for 85% of the variability observed in captures. -
The Taxonomic Position and the Scientific Name of the Big Tree Known As Sequoia Gigantea
The Taxonomic Position and the Scientific Name of the Big Tree known as Sequoia gigantea HAROLD ST. JOHN and ROBERT W. KRAUSS l FOR NEARLY A CENTURY it has been cus ing psychological document, but its major,ity tomary to classify the big tree as Sequoia gigan vote does not settle either the taxonomy or tea Dcne., placing it in the same genus with the nomenclature of the big tree. No more the only other living species, Sequoia semper does the fact that "the National Park Service, virens (Lamb.) End!., the redwood. Both the which has almost exclusive custodY of this taxonomic placement and the nomenclature tree, has formally adopted the name Sequoia are now at issue. Buchholz (1939: 536) pro gigantea for it" (Dayton, 1943: 210) settle posed that the big tree be considered a dis the question. tinct genus, and he renamed the tree Sequoia The first issue is the generic status of the dendron giganteum (Lind!.) Buchholz. This trees. Though the two species \differ con dassification was not kindly received. Later, spicuously in foliage and in cone structure, to obtain the consensus of the Calif.ornian these differences have long been generally botanists, Dayton (1943: 209-219) sent them considered ofspecific and notofgeneric value. a questionnaire, then reported on and sum Sequoiadendron, when described by Buchholz, marized their replies. Of the 29 answering, was carefully documented, and his tabular 24 preferred the name Sequoia gigantea. Many comparison contains an impressive total of of the passages quoted show that these were combined generic and specific characters for preferences based on old custom or sentiment, his monotypic genus. -
Supporting Information
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. -
Flora of South Australia 5Th Edition | Edited by Jürgen Kellermann
Flora of South Australia 5th Edition | Edited by Jürgen Kellermann KEY TO FAMILIES1 J.P. Jessop2 The sequence of families used in this Flora follows closely the one adopted by the Australian Plant Census (www.anbg.gov. au/chah/apc), which in turn is based on that of the Angiosperm Phylogeny Group (APG III 2009) and Mabberley’s Plant Book (Mabberley 2008). It differs from previous editions of the Flora, which were mainly based on the classification system of Engler & Gilg (1919). A list of all families recognised in this Flora is printed in the inside cover pages with families already published highlighted in bold. The up-take of this new system by the State Herbarium of South Australia is still in progress and the S.A. Census database (www.flora.sa.gov.au/census.shtml) still uses the old classification of families. The Australian Plant Census web-site presents comparison tables of the old and new systems on family and genus level. A good overview of all families can be found in Heywood et al. (2007) and Stevens (2001–), although these authors accept a slightly different family classification. A number of names with which people using this key may be familiar but are not employed in the system used in this work have been included for convenience and are enclosed on quotation marks. 1. Plants reproducing by spores and not producing flowers (“Ferns and lycopods”) 2. Aerial shoots either dichotomously branched, with scale leaves and 3-lobed sporophores or plants with fronds consisting of a simple or divided sterile blade and a simple or branched spikelike sporophore .................................................................................. -
Common Name: Bald Cypress Scientific Name: Taxodium Distichum Order: Arecales Family: Cupressaceae Wetland Plant Status: Oblig
Common Name: Bald Cypress Scientific Name: Taxodium distichum Order: Arecales Family: Cupressaceae Wetland Plant Status: Obligatory Ecology & Description Bald cypress needs water to thrive. It can be found naturally on the banks of a water body or in the center of the water. When planted, it can survive more upland. The cypress tree grows very slowly and will die if submerged in water. It is a slow growing, long-lived deciduous conifer. The trees frequently get over 100 feet tall with a diameter of 6 feet. The trunk is normally tapered. The leaves are needle-like but appear flattened. The bark is very thin and fibrous with narrow furrows. The bald cypress produces cone fruit and cypress knees. Habitat Bald cypress trees are confined to wet soils were water is almost permanent. It is usually found on flat elevations. Distribution Bald cypress is widely distributed along the Atlantic Coast and Gulf Coast, but can be found inland along streams. Native/Invasive Status Bald cypress is native to lower 48 states of the United States. Wildlife Uses Squirrels and many different bird species use the seeds as food. Bald cypress domes also create watering holes for a variety of birds and mammals. Amphibians and reptiles will also use bald cypress domes as breeding grounds. Management & Control Techniques When regenerating cypress, canopy thinning is a must. Overhead thinning will allow for seedlings to grow. The seedling cannot be submerged in water. Seedlings cannot germinate in flooded areas. The seedling must be somewhat taller than the floodwaters for survival. Good seed production occurs about every three years and is dispersed better with flood waters.