Assessment of Invasive Species in Alaska and Its National Forests August 30, 2005
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Two New Chrysomyxa Rust Species on the Endemic Plant, Picea Asperata in Western China, and Expanded Description of C
Phytotaxa 292 (3): 218–230 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.292.3.2 Two new Chrysomyxa rust species on the endemic plant, Picea asperata in western China, and expanded description of C. succinea JING CAO1, CHENG-MING TIAN1, YING-MEI LIANG2 & CHONG-JUAN YOU1* 1The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University, Beijing 100083, China 2Museum of Beijing Forestry University, Beijing 100083, China *Corresponding author: [email protected] Abstract Two new rust species, Chrysomyxa diebuensis and C. zhuoniensis, on Picea asperata are recognized by morphological characters and DNA sequence data. A detailed description, illustrations, and discussion concerning morphologically similar and phylogenetically closely related species are provided for each species. From light and scanning electron microscopy observations C. diebuensis is characterized by the nailhead to peltate aeciospores, with separated stilt-like base. C. zhuoni- ensis differs from other known Chrysomyxa species in the annulate aeciospores with distinct longitudinal smooth cap at ends of spores, as well as with a broken, fissured edge. Analysis based on internal transcribed spacer region (ITS) partial gene sequences reveals that the two species cluster as a highly supported group in the phylogenetic trees. Correlations between the morphological and phylogenetic features are discussed. Illustrations and a detailed description are also provided for the aecia of C. succinea in China for the first time. Keywords: aeciospores, molecular phylogeny, spruce needle rust, taxonomy Introduction Picea asperata Mast.is native to western China, widely distributed in Qinghai, Gansu, Shaanxi and western Sichuan. -
Alpine Larch
Alpine Larch Pinaceae Pine family Stephen F. Arno Alpine larch (Lurix lyallii), also called subalpine larch and Lyall larch, is a deciduous conifer. Its com- mon name recognizes that this species oRen grows higher up on cool exposures than any other trees, thereby occupying what would otherwise be an al- pine tundra. Both early-day botanical explorers and modern visitors to the high mountains have noted this tree’s remarkable ability to form pure groves above the limits of evergreen conifers. Alpine larch inhabits remote high-mountain terrain and its wood has essentially no commercial value; however this tree is ecologically interesting and esthetically at- tractive. Growing in a very cold, snowy, and often windy environment, alpine larch usually remains small and stunted, but in windsheltered basins it sometimes attains large size-maximum 201 cm (79 in) in d.b.h. and 29 m (95 ft) in height. This species is distinguished from its lower elevation relative western larch (Larix occidentalis) by the woolly hairs that cover its buds and recent twigs, and frequently by its broad, irregular crown. Habitat Figure l-The native range of alpine larch. Native Range amounts atop numerous other ranges and peaks in western Montana and northern Idaho (4). In British Alpine larch (fig. 1) occupies a remote and rigorous Columbia and Alberta, alpine larch is common along environment, growing in and near the timberline on the Continental Divide and adjacent ranges, and in high mountains of the inland Pacific Northwest. Al- the Purcell and southern Selkirk Ranges. though alpine larch is found in both the Rocky Moun- In the Cascade Range alpine larch is found prin- tains and the Cascades, the two distributions are cipally east of the Cascade Divide and extends from separated at their closest points by 200 km (125 mi) the Wenatchee Mountains (47” 25’ N.) in central in southern British Columbia. -
DEFOLIATORS Insect Sections
Alaska. Reference is made to this map in selected DEFOLIATORS insect sections. (Precipitation information from Schwartz, F.K., and Miller, J.F. 1983. Probable maximum precipitation and snowmelt criteria for Fewer defoliator plots (27 plots) were visited during southeast Alaska: National Weather Service the 1999 aerial survey than in previous years (52 plots) Hydrometeorological Report No. 54. 115p. GIS layer throughout southeast Alaska. An effort was made to created by: Tim Brabets, 1997. distribute these plots evenly across the archipelago. URL:http://agdc.usgs.gov/data/usgs/water) The objectives during the 1999 season were to: ¨ Spend more time covering the landscape during Spruce Needle Aphid the aerial survey, Elatobium abietinum Walker ¨ Allow more time to land and identify unknown mortality and defoliation, and Spruce needle aphids feed on older needles of Sitka ¨ Avoid visit sites that were hard to get to and had spruce, often causing significant amounts of needle few western hemlocks. drop (defoliation). Defoliation by aphids cause reduced tree growth and can predispose the host to Hemlock sawfly and black-headed budworm larvae other mortality agents, such as the spruce beetle. counts were generally low in 1999 as they were in Severe cases of defoliation alone may result in tree 1998. The highest sawfly larvae counts were from the mortality. Spruce in urban settings and along marine plots in Thorne Bay and Kendrick Bay, Prince of shorelines are most seriously impacted. Spruce aphids Wales Island. Larval counts are used as a predictive feed primarily in the lower, innermost portions of tree tool for outbreaks of defoliators. For example, if the crowns, but may impact entire crowns during larval sample is substantially greater in 1999, then an outbreaks. -
Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
Integration of Entomopathogenic Fungi Into IPM Programs: Studies Involving Weevils (Coleoptera: Curculionoidea) Affecting Horticultural Crops
insects Review Integration of Entomopathogenic Fungi into IPM Programs: Studies Involving Weevils (Coleoptera: Curculionoidea) Affecting Horticultural Crops Kim Khuy Khun 1,2,* , Bree A. L. Wilson 2, Mark M. Stevens 3,4, Ruth K. Huwer 5 and Gavin J. Ash 2 1 Faculty of Agronomy, Royal University of Agriculture, P.O. Box 2696, Dangkor District, Phnom Penh, Cambodia 2 Centre for Crop Health, Institute for Life Sciences and the Environment, University of Southern Queensland, Toowoomba, Queensland 4350, Australia; [email protected] (B.A.L.W.); [email protected] (G.J.A.) 3 NSW Department of Primary Industries, Yanco Agricultural Institute, Yanco, New South Wales 2703, Australia; [email protected] 4 Graham Centre for Agricultural Innovation (NSW Department of Primary Industries and Charles Sturt University), Wagga Wagga, New South Wales 2650, Australia 5 NSW Department of Primary Industries, Wollongbar Primary Industries Institute, Wollongbar, New South Wales 2477, Australia; [email protected] * Correspondence: [email protected] or [email protected]; Tel.: +61-46-9731208 Received: 7 September 2020; Accepted: 21 September 2020; Published: 25 September 2020 Simple Summary: Horticultural crops are vulnerable to attack by many different weevil species. Fungal entomopathogens provide an attractive alternative to synthetic insecticides for weevil control because they pose a lesser risk to human health and the environment. This review summarises the available data on the performance of these entomopathogens when used against weevils in horticultural crops. We integrate these data with information on weevil biology, grouping species based on how their developmental stages utilise habitats in or on their hostplants, or in the soil. -
Danske Snyltehvepse Og -Fluer Fra Fyrrevikleren, Rhyacionia Buoliana Schiff
Danske snyltehvepse og -fluer fra fyrrevikleren, Rhyacionia buoliana Schiff. (Lepid., Tortricidaey af PETER ESBJERG (With a summary: Danish hymenopterous and dipterous parasites from the pine shoot moth, Rhyacionia buoliana Schiff.). Fyrrevikleren er på grund af sin forstlige betydning blevet fulgt med be tydelig interesse i Europa de senere år. Også i Danmark har den været genstand for øget opmærksomhed, hvad især hænger sammen med den stigende anvendelse af contortafyr (Pinus contorta Loud.) i dansk skov brug (B. Bejer-Petersen, 1966 ). Contortafyrren kan nemlig angribes meget stærkt, da den hører til blandt fyrreviklerens foretrukne værtstræer. Deri mod finder man her i landet sjældent større angreb på andre fyrretræer (Esbjerg og Feilberg, 1970). De fleste udenlandske undersøgelser har vist, at fyrrevikleren ofte er udsat for en ikke ringe parasitering af en række snyltehvepse og -fluer. Naturlige spørgsmål angående det hjemlige fyrreviklerproblem har derfor været, om vor fyrreviklerbestand også parasiteres, og i bekræftende fald da i hvilket omfang, og om parasitterne er de samme som i nabolandene. Undersøgelsen heraf er begrænset til contortafyr med udeladelse af æg• parasitter, der antagelig kun findes i ringe antal. MATERlAL E OG METODIK Indsamling Indsamlingerne er foretaget i juni måned, da de angrebne skud på denne tid er særlig lette at erkende, og klækningen er nært forestående. I materialet indgår 15 lokaliteter, der repræsenterer fyrreviklerangreb af varierende tæthed og styrke, i aldrene 1-1 O år (tabel 1 og fig. 1). Prø verne udtoges systematisk efter groftmasket kvadratnet i årene 1969-70 og for et enkelt områdes vedkommende også i 1968. Der indsamledes ialt ca. 9000 skud. -
Root Weevils Fact Sheet No
Root Weevils Fact Sheet No. 5.551 Insect Series|Home and Garden by W.S. Cranshaw* None of the root weevils can fly and A root weevil is a type of “snout beetle” they are night active, hiding during the Quick Facts that develops on the roots of various plants. day around the base of host plants, usually Adult stages produce more conspicuous under a bit of cover. About an hour after • Root weevils can be common plant damage, cutting angular notches along sunset they become active and crawl onto insects that develop on roots the edge of leaves when they feed at night. the plants to feed on leaves, producing their of many garden plants. Adult root weevils also may attract attention characteristic angular notches. If disturbed, • Adult root weevils chew when they wander into buildings, acting as a root weevils will readily drop from plants and distinctive notches along the temporary “nuisance invader”. play dead. The most common root weevils found Adults typically live for at least a couple edges of leaves at night. in Colorado are strawberry root weevil of months, and some may be present into • Some kinds of root weevils (Otiorhynchus ovatus), rough strawberry autumn. Most eggs are laid in late spring and often wander into homes but root weevil (O. rugostriatus), black vine early summer with females squeezing eggs cause no injury indoors. weevil (O. sulcatus) and lilac root weevil into soil cracks. A few days after they are (O. meridionalis). Dyslobus decoratus is laid, eggs hatch and the larvae move to the • Insecticides applied on the established in some areas and chews leaves roots where they feed. -
Larix Decidua Miller Taxonomy Author, Year Miller Synonym Larix Europaea DC; Larix Sudetica Domin; Pinus Larix L
Forest Ecology and Forest Management Group Tree factsheet images at pages 3 and 4 Larix decidua Miller taxonomy author, year Miller synonym Larix europaea DC; Larix sudetica Domin; Pinus larix L. Family Pinaceae Eng. Name European larch, Common larch Dutch name Europese lariks (Boom, 2000) Europese lork (Heukels’ Flora, 2005) subspecies - varieties L. decidua var. polonica (Racib) Ostenf. & Syrach Larsen (syn. L. polonica Racib.) L. decidua var. carpatica Domin (syn. L. carpatica Domin.) hybrids Larix x marschlinsii Coaz (L. decidua x L. kaempferi) (syn. Larix x eurolepis Henry) cultivars, frequently planted - references Earle, C.J. Gymnosperm database www.conifers.org USDA Forest Service www.pfaf.org/database/index.php Westra, J.J. Het geslacht Larix. In Schmidt (ed.). 1987. Ned. Boomsoorten 1 Syllabus vakgroep Bosteelt en Bosecologie, Landbouwuniversiteit Wageningen Plants for a Future Database; www.pfaf.org/index.html morphology crown habit tree, pyramidal max. height (m) Europe: 30-50 The Netherlands: 30 max. dbh (cm) 100-200 oldest tree year 988 AC, tree ring count, Val Malenco, Italy. actual size Europe year …, d(130) 95, h 46, Glenlee Park, Dumfries and Galloway, UK. year …, d(130) 271, h 30, Ulten Valley, Saint Nicholas, Italy. actual size Netherlands year 1844, d…, h …, Schovenhorst, Putten year 1830-1840, d(130) 114, h 17 year 1850-1860, d(130) 115, h 20 year 1860-1870, d(130) 97, h 28 leaf length (cm) 2-4 single leaf petiole (cm) 0 leaf colour upper surface green leaf colour under surface green leaves arrangement alternate flowering March - May flowering plant monoecious flower monosexual flower diameter (cm) ? pollination wind fruit; length cone; 3-4 cm fruit petiole (cm) 0,3 seed; length samara (=winged nut); … cm seed-wing length (cm) weight 1000 seeds (g) 5,0-5,9 seeds ripen October same year seed dispersal wind habitat natural distribution Alps, Central Europe in N.W. -
Pinus Nigra V
Technical guidelines for genetic conservation and use European black pine Pinus nigra V. Isajev1, B. Fady2, H. Semerci3 and V. Andonovski4 1 Forestry Faculty of Belgrade University, Belgrade, Serbia and Montenegro EUFORGEN 2 INRA, Mediterranean Forest Research Unit, Avignon, France 3 Forest Tree Seeds&Tree Breeding Research Directorate, Ankara,Turkey 4 Faculty of Forestry, Skopje, Macedonia FYR These Technical Guidelines are intended to assist those who cherish the valuable European black pine genepool and its inheritance, through conserving valuable seed sources or use in practical forestry. The focus is on conserving the genetic diversity of the species at the European scale. The recommendations provided in this module should be regarded as a commonly agreed basis to be complemented and further developed in local, national or regional conditions. The Guidelines are based on the available knowledge of the species and on widely accepted methods for the conservation of forest genetic resources. Biology and ecology although seed yield is abundant only every 2–4 years. Trees reach sexual maturity at 15–20 years in The European black pine (Pinus their natural habitat. Flowers nigra Arnold) grows up to 30 appear in May. Female inflores- (rarely 40–50) m tall, with a trunk cences are reddish, and male that is usually straight. The bark catkins are yellow. Fecundation is light grey to dark grey-brown, occurs 13 months after pollina- deeply furrowed longitudinally on tion. Cones are sessile and hori- older trees. The crown is broadly zontally spreading, 4–8 cm long, conical on young trees, umbrel- 2–4 cm wide, yellow-brown or la-shaped on older trees, light yellow and glossy. -
Northern Fen Communitynorthern Abstract Fen, Page 1
Northern Fen CommunityNorthern Abstract Fen, Page 1 Community Range Prevalent or likely prevalent Infrequent or likely infrequent Absent or likely absent Photo by Joshua G. Cohen Overview: Northern fen is a sedge- and rush-dominated 8,000 years. Expansion of peatlands likely occurred wetland occurring on neutral to moderately alkaline following climatic cooling, approximately 5,000 years saturated peat and/or marl influenced by groundwater ago (Heinselman 1970, Boelter and Verry 1977, Riley rich in calcium and magnesium carbonates. The 1989). community occurs north of the climatic tension zone and is found primarily where calcareous bedrock Several other natural peatland communities also underlies a thin mantle of glacial drift on flat areas or occur in Michigan and can be distinguished from shallow depressions of glacial outwash and glacial minerotrophic (nutrient-rich) northern fens, based on lakeplains and also in kettle depressions on pitted comparisons of nutrient levels, flora, canopy closure, outwash and moraines. distribution, landscape context, and groundwater influence (Kost et al. 2007). Northern fen is dominated Global and State Rank: G3G5/S3 by sedges, rushes, and grasses (Mitsch and Gosselink 2000). Additional open wetlands occurring on organic Range: Northern fen is a peatland type of glaciated soils include coastal fen, poor fen, prairie fen, bog, landscapes of the northern Great Lakes region, ranging intermittent wetland, and northern wet meadow. Bogs, from Michigan west to Minnesota and northward peat-covered wetlands raised above the surrounding into central Canada (Ontario, Manitoba, and Quebec) groundwater by an accumulation of peat, receive inputs (Gignac et al. 2000, Faber-Langendoen 2001, Amon of nutrients and water primarily from precipitation et al. -
Retrospective Analysis of Lophodermium Seditiosum Epidemics in Estonia
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Directory of Open Access Journals Acta Silv. Lign. Hung., Spec. Edition (2007) 31-45 Retrospective Analysis of Lophodermium seditiosum Epidemics in Estonia * Märt HANSO – Rein DRENKHAN Estonian University of Life Sciences, Institute of Forestry and Rural Engineering, Tartu, Estonia Abstract – The needle trace method (NTM), created and developed by the Finnish forest pathologists prof. T. Kurkela, dr. R. Jalkanen and T. Aalto during the last decade of the XX century, has been already used by several researchers of different countries for retrospective analysis of needle diseases (Hypodermella sulcigena , by R. Jalkanen et al. in Finland) or herbivorous insect pests of Scots pine (Diprion pini, by T. Kurkela et al. in Finland; Bupalus piniaria , by H. Armour et al. in Scotland), but as well of pests of Sitka spruce (Gilpinia hercyniae , by D.T. Williams et al. in England). Scots pine in forest nurseries and young plantations of Estonia is often but irregularly suffering from the epidemics of the needle cast fungus Lophodermium seditiosum . Current environmental regulations exclude from the regulatory (control) measures all the others except of well-argued prophylactic systems, built up on reliable prognoses. The last is inconceivable without the availability of a reliable, as well, and long- lasting retrospective time-series of L. seditiosum epidemics, which, as it is known from the last half of the XX century, are occupying large forest areas, usually not least than a half of (the small) Estonia. An appropriate time-series would be useful, as well, for the more basic understanding of the accelerated mortality processes during the stand formation in early pole-age Scots pine plantations. -
Evidence and Implications of Recent and Projected Climate Change in Alaska’S Forest Ecosystems 1, 2 1 3 4 JANE M
Evidence and implications of recent and projected climate change in Alaska’s forest ecosystems 1, 2 1 3 4 JANE M. WOLKEN, TERESA N. HOLLINGSWORTH, T. SCOTT RUPP, F. STUART CHAPIN, III, SARAH F. TRAINOR, 5 6 7 3 8 TARA M. BARRETT, PATRICK F. SULLIVAN, A. DAVID MCGUIRE, EUGENIE S. EUSKIRCHEN, PAUL E. HENNON, 9 10 11 8 1 ERIK A. BEEVER, JEFF S. CONN, LISA K. CRONE, DAVID V. D ’AMORE, NANCY FRESCO, 8 3 12 11 13 THOMAS A. HANLEY, KNUT KIELLAND, JAMES J. KRUSE, TRISTA PATTERSON, EDWARD A. G. SCHUUR, 14 14 DAVID L. VERBYLA, AND JOHN YARIE 1Scenarios Network for Alaska and Arctic Planning, University of Alaska, 3352 College Road, Fairbanks, Alaska 99709 USA 2United States Department of Agriculture Forest Service, Pacific Northwest Research Station, Boreal Ecology Cooperative Research Unit, P.O. Box 756780, University of Alaska, Fairbanks, Alaska 99775 USA 3Institute of Arctic Biology, University of Alaska, Fairbanks, Alaska 99775 USA 4Alaska Center for Climate Assessment and Policy, University of Alaska, 3352 College Road, Fairbanks, Alaska 99709 USA 5United States Department of Agriculture Forest Service, Pacific Northwest Research Station, Anchorage Forestry Sciences Laboratory, 3301 C Street, Suite 200, Anchorage, Alaska 99503 USA 6Environment and Natural Resources Institute, Department of Biological Sciences, University of Alaska, Anchorage, Alaska 99508 USA 7United States Geological Survey, Alaska Cooperative Fish and Wildlife Research Unit, University of Alaska, Fairbanks, Alaska 99775 USA 8United States Department of Agriculture Forest