Classification, Description, and Dynamics of Plant Communities After Fire in the Taiga of Interior Alaska
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Coptis Trifolia Conservation Assessment
CONSERVATION ASSESSMENT for Coptis trifolia (L.) Salisb. Originally issued as Management Recommendations December 1998 Marty Stein Reconfigured-January 2005 Tracy L. Fuentes USDA Forest Service Region 6 and USDI Bureau of Land Management, Oregon and Washington CONSERVATION ASSESSMENT FOR COPTIS TRIFOLIA Table of Contents Page List of Tables ................................................................................................................................. 2 List of Figures ................................................................................................................................ 2 Summary........................................................................................................................................ 4 I. NATURAL HISTORY............................................................................................................. 6 A. Taxonomy and Nomenclature.......................................................................................... 6 B. Species Description ........................................................................................................... 6 1. Morphology ................................................................................................................... 6 2. Reproductive Biology.................................................................................................... 7 3. Ecological Roles ............................................................................................................. 7 C. Range and Sites -
Vegetative Ecology of a Montane Mire, Crater Lake National
AJ ABSTRACT OF THE THESIS OF Susan Cornelia Seyer for the degree of Master of Science in Botany and Plant Pathology presented on December 14, 1979 Title: VEGETATIVE ECOLOGY OF A MONTANE MIRE, CRATER LAKE NATIONAL PARK, OREGON Redacted for Privacy Abstract approved: Jerry F. Franklin Mires, or peat-producing ecosystems, dominated by sedges, shrubs, and brown mosses, are common features in Cascade subalpine regions, occurring where moisture accumulates in small basins or on poorly-drained slopes. Although descriptions and classifications have been developed for mire vegetation in much of the world, there is little information of even a descriptive nature for these montane mires in Oregon and Washington. This thesis reports on phytosocia- logical structure, env'ironental relations, and successional trends in one such mire in the Oregon Cascade mountains. To characterize the general phytosociological structure of the mire vegetation at Sphagnum Bog, Crater Lake National Park, quantitative species cover data were used in conjunction with a Braun-Blanquet tabular analysis and two-dimensional stand ordinations, reciprocal averaging and a Bray-Curtis polar ordination. Defined community types correspond to physiognomic types as follows: Carex rostrata (reedswamp); Eleocharis pauciflora-Carex limosa, Eleocharis pauciflora/bryophytes (low sedge fens); Carex sichensis (tall sedge fen); Vaccinium/ Aulacomnium palustre, Vaccinium occidentala/Carex sitchensis (shrub thickets; Alnus incana/Brachythacium sp. and Salix barclayi (marginal carrs).Phases were defined when appropriate. A vegetation map was made to illustrate the locations and extent of the variouscommunities. Comparisons with other montane mires in thearea determined that the physiognomic units defined are repeatable when appropriate habitat conditions are present, and that they usually includemany of the same characteristic species, the dominant mosses being particularly constant. -
Economic and Ethnic Uses of Bryophytes
Economic and Ethnic Uses of Bryophytes Janice M. Glime Introduction Several attempts have been made to persuade geologists to use bryophytes for mineral prospecting. A general lack of commercial value, small size, and R. R. Brooks (1972) recommended bryophytes as guides inconspicuous place in the ecosystem have made the to mineralization, and D. C. Smith (1976) subsequently bryophytes appear to be of no use to most people. found good correlation between metal distribution in However, Stone Age people living in what is now mosses and that of stream sediments. Smith felt that Germany once collected the moss Neckera crispa bryophytes could solve three difficulties that are often (G. Grosse-Brauckmann 1979). Other scattered bits of associated with stream sediment sampling: shortage of evidence suggest a variety of uses by various cultures sediments, shortage of water for wet sieving, and shortage around the world (J. M. Glime and D. Saxena 1991). of time for adequate sampling of areas with difficult Now, contemporary plant scientists are considering access. By using bryophytes as mineral concentrators, bryophytes as sources of genes for modifying crop plants samples from numerous small streams in an area could to withstand the physiological stresses of the modern be pooled to provide sufficient material for analysis. world. This is ironic since numerous secondary compounds Subsequently, H. T. Shacklette (1984) suggested using make bryophytes unpalatable to most discriminating tastes, bryophytes for aquatic prospecting. With the exception and their nutritional value is questionable. of copper mosses (K. G. Limpricht [1885–]1890–1903, vol. 3), there is little evidence of there being good species to serve as indicators for specific minerals. -
Vermont Natural Community Types
Synonymy of Vermont Natural Community Types with National Vegetation Classification Associations Eric Sorenson and Bob Zaino Natural Heritage Inventory Vermont Fish and Wildlife Department October 17, 2019 Vermont Natural Community Type Patch State National and International Vegetation Classification. NatureServe. 2019. Size Rank NatureServe Explorer: An online encyclopedia of life. NatureServe, Arlington, Virginia. Spruce-Fir-Northern Hardwood Forest Formation Subalpine Krummholz S S1 Picea mariana - Abies balsamea / Sibbaldiopsis tridentata Shrubland (CEGL006038); (Picea mariana, Abies balsamea) / Kalmia angustifolia - Ledum groenlandicum Dwarf-shrubland Montane Spruce-Fir Forest L-M S3 Picea rubens - Abies balsamea - Sorbus americana Forest (CEGL006128) Variant: Montane Fir Forest L-M S3 Abies balsamea - (Betula papyrifera var. cordifolia) Forest (CEGL006112) Variant: Montane Spruce Forest Lowland Spruce-Fir Forest L-M S3 Picea mariana - Picea rubens / Pleurozium schreberi Forest (CEGL006361) Variant: Well-Drained Lowland Spruce- L S2 Picea rubens - Abies balsamea - Betula papyrifera Forest (CEGL006273); Fir Forest Picea mariana - Picea rubens / Rhododendron canadense / Cladina spp. Woodland (CEGL006421) Montane Yellow Birch-Red Spruce Forest M S3 Betula alleghaniensis - Picea rubens / Dryopteris campyloptera Forest (CEGL006267) Variant: Montane Yellow Birch-Sugar L S3 Maple-Red Spruce Forest Red Spruce-Northern Hardwood Forest M S5 Betula alleghaniensis - Picea rubens / Dryopteris campyloptera Forest (CEGL006267) Red Spruce-Heath -
Appendix 2: Plant Lists
Appendix 2: Plant Lists Master List and Section Lists Mahlon Dickerson Reservation Botanical Survey and Stewardship Assessment Wild Ridge Plants, LLC 2015 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Acalypha rhomboidea Native 1 Forb 9 Acer palmatum Invasive 0 Tree 1 Acer pensylvanicum Native 7 Tree 2 Acer platanoides Invasive 0 Tree 4 Acer rubrum Native 3 Tree 27 Acer saccharum Native 5 Tree 24 Achillea millefolium Native 0 Forb 18 Acorus calamus Alien 0 Forb 1 Actaea pachypoda Native 5 Forb 10 Adiantum pedatum Native 7 Fern 7 Ageratina altissima v. altissima Native 3 Forb 23 Agrimonia gryposepala Native 4 Forb 4 Agrostis canina Alien 0 Graminoid 2 Agrostis gigantea Alien 0 Graminoid 8 Agrostis hyemalis Native 2 Graminoid 3 Agrostis perennans Native 5 Graminoid 18 Agrostis stolonifera Invasive 0 Graminoid 3 Ailanthus altissima Invasive 0 Tree 8 Ajuga reptans Invasive 0 Forb 3 Alisma subcordatum Native 3 Forb 3 Alliaria petiolata Invasive 0 Forb 17 Allium tricoccum Native 8 Forb 3 Allium vineale Alien 0 Forb 2 Alnus incana ssp rugosa Native 6 Shrub 5 Alnus serrulata Native 4 Shrub 3 Ambrosia artemisiifolia Native 0 Forb 14 Amelanchier arborea Native 7 Tree 26 Amphicarpaea bracteata Native 4 Vine, herbaceous 18 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Anagallis arvensis Alien 0 Forb 4 Anaphalis margaritacea Native 2 Forb 3 Andropogon gerardii Native 4 Graminoid 1 Andropogon virginicus Native 2 Graminoid 1 Anemone americana Native 9 Forb 6 Anemone quinquefolia Native 7 Forb 13 Anemone virginiana Native 4 Forb 5 Antennaria neglecta Native 2 Forb 2 Antennaria neodioica ssp. -
Molecular Phylogeny of Chinese Thuidiaceae with Emphasis on Thuidium and Pelekium
Molecular Phylogeny of Chinese Thuidiaceae with emphasis on Thuidium and Pelekium QI-YING, CAI1, 2, BI-CAI, GUAN2, GANG, GE2, YAN-MING, FANG 1 1 College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. 2 College of Life Science, Nanchang University, 330031 Nanchang, China. E-mail: [email protected] Abstract We present molecular phylogenetic investigation of Thuidiaceae, especially on Thudium and Pelekium. Three chloroplast sequences (trnL-F, rps4, and atpB-rbcL) and one nuclear sequence (ITS) were analyzed. Data partitions were analyzed separately and in combination by employing MP (maximum parsimony) and Bayesian methods. The influence of data conflict in combined analyses was further explored by two methods: the incongruence length difference (ILD) test and the partition addition bootstrap alteration approach (PABA). Based on the results, ITS 1& 2 had crucial effect in phylogenetic reconstruction in this study, and more chloroplast sequences should be combinated into the analyses since their stability for reconstructing within genus of pleurocarpous mosses. We supported that Helodiaceae including Actinothuidium, Bryochenea, and Helodium still attributed to Thuidiaceae, and the monophyletic Thuidiaceae s. lat. should also include several genera (or species) from Leskeaceae such as Haplocladium and Leskea. In the Thuidiaceae, Thuidium and Pelekium were resolved as two monophyletic groups separately. The results from molecular phylogeny were supported by the crucial morphological characters in Thuidiaceae s. lat., Thuidium and Pelekium. Key words: Thuidiaceae, Thuidium, Pelekium, molecular phylogeny, cpDNA, ITS, PABA approach Introduction Pleurocarpous mosses consist of around 5000 species that are defined by the presence of lateral perichaetia along the gametophyte stems. Monophyletic pleurocarpous mosses were resolved as three orders: Ptychomniales, Hypnales, and Hookeriales (Shaw et al. -
Correction To: Testing the Moss Layer Transfer Technique on Mineral Well Pads Constructed in Peatlands
Wetlands Ecol Manage (2018) 26:489–490 https://doi.org/10.1007/s11273-018-9608-9 CORRECTION Correction to: Testing the moss layer transfer technique on mineral well pads constructed in peatlands Marie-Eve Gauthier . Line Rochefort . Leonie Nadeau . Sandrine Hugron . Bin Xu Published online: 28 May 2018 Ó Springer Science+Business Media B.V., part of Springer Nature 2018 Correction to: Wetlands Ecol Manage https://doi.org/10.1007/s11273-017-9532-4 In the original publication, the Table 1 was published incorrectly. The correct version of Table 1 is given in this correction. The original article has been corrected. The original article can be found online at https:// doi.org/10.1007/s11273-017-9532-4. M.-E. Gauthier Á L. Rochefort (&) Á S. Hugron Department of Plant Sciences and Centre for Northern Studies, Universite´ Laval, Que´bec, QC G1V 0A6, Canada e-mail: [email protected] L. Nadeau Á B. Xu NAIT Boreal Research Institute, Peace River, AB T8S 1R2, Canada 123 490 Wetlands Ecol Manage (2018) 26:489–490 Table 1 Description of fen plant communities used as source of propagules (donor sites) for the moss layer transfer experiment Treed Rich Fen Cover Shrubby Rich Fen Cover Plant composition Trees Picea mariana 10 – Shrubs Vaccinium vitis-idaea 12 Salix spp. 15 Larix laricina 9 Betula glandulosa 2 Chamaedaphne calyculata 8 Empetrum nigrum 4 Rhododendron groenlandicum 4 Salix spp. 4 Herbs Carex aquatilis 3 Carex aquatilis 7 Carex tenuiflora * Comarum palustre 2 Carex magellanica ssp. irrigua 1 Mosses Sphagum fuscum 55 Sphagnum angustifolium 30 Aulacomnium palustre 3 Tomentypnum nitens 15 Aulacomnium palustre 3 Water chem. -
Vegetation at the Taiga Forest–Steppe Borderline in the Western Khentey Mountains, Northern Mongolia
Ann. Bot. Fennici 42: 411–426 ISSN 0003-3847 Helsinki 19 December 2005 © Finnish Zoological and Botanical Publishing Board 2005 Vegetation at the taiga forest–steppe borderline in the western Khentey Mountains, northern Mongolia Choimaa Dulamsuren1, Markus Hauck2 & Michael Mühlenberg1 1) Center of Nature Conservation, University of Göttingen, Von-Siebold-Straße 2, D-37075 Göttingen, Germany (e-mail: [email protected]) 2) Albrecht von Haller Institute of Plant Sciences, University of Göttingen, Untere Karspüle 2, D-37073 Göttingen, Germany (e-mail: [email protected]) Received 31 Aug. 2004, revised version received 11 Nov. 2004, accepted 7 Jan. 2005 Dulamsuren, C., Hauck, M. & Mühlenberg, M. 2005: Vegetation at the taiga forest–steppe border- line in the western Khentey Mountains, northern Mongolia. — Ann. Bot. Fennici 42: 411–426. Vegetation of an area of 500 km2 in the western Khentey Mountains, northern Mon- golia is phytosociologically classified with the help of 254 relevés. Twenty-one main vegetation units are described. The study area is situated at the interface between the western Siberian dark taiga, the eastern Siberian light taiga and the Mongolian-Daurian forest steppe. A small-scale pattern of these three major vegetation types was found depending on site characteristics. Dark taiga forests of Pinus sibirica, Abies sibirica, Picea obovata, and Larix sibirica grow at the most humid sites. Light taiga forests dominated by Larix sibirica and Betula platyphylla occur on relatively dry northern slopes of the lower montane belt. Sun-exposed, southern slopes of the lower montane belt are covered by montane meadow and mountain steppe. DCA ordination suggests that the distribution of vegetation types depends on water supply and altitude. -
Here Is Glaucum) Looks Like Tiny Pine Seedlings on This Disturbed Soil Along Forest Edge
Pennsylvania Natural Heritage Program informationinformation forfor thethe conservationconservation ofof biodiversitybiodiversity Wild Heritage News January—March 2014 Bryophytes and Lichens of Dry Oak Heath Forest Communities Inside This Issue by Scott Schuette Bryophytes and Pg 1 Lichens Pennsylvania is flush with a diversity of biodiversity ripe for exploration if one just Edge of Range Pg 4 forest communities, some garnering looks a little bit closer at the smaller Species special attention due to the quality of organisms living within this forest plant diversity and others for the community. Preserving Records Pg 6 hardwood resources they provide. The of our Work dry oak heath forests fall into the latter Bryophytes and lichens are present in category. These forest communities are every forest community, regardless of size Notes from the Pg 7 found throughout the state occurring on and condition. It is well-documented that Field moderately dry to xeric, acidic sites that bryophytes and lichens are sensitive to Measures of Pg 12 usually have shallow or sometimes sandy human disturbance and, as a result, have Progress soils. The dominant tree canopy is been used as indicators of habitat quality. chestnut oak (Quercus montana) mixed These organisms tend to live on the trees with black oak (Quercus velutina), white and shrubs as epiphytes (rootless, oak (Quercus alba), and red maple (Acer independent living plants), but they can rubrum). Other tree species that are also completely cover boulders or reside commonly present in the subcanopy Photo Banner: include sassafras (Sassafras albidum), Scott Schuette sweet birch (Betula lenta), black gum (Nyssa sylvatica), and eastern white pine The stair-step moss (Pinus strobus). -
Atlantic Woodlands in the Lake District Mosses & Liverworts
LIVERWORTS generally have two rows of leaves, one up each side of the stem We are Plantlife Further information For over 25 years, Plantlife has had a single ideal Bazzania trilobata Greater whipwort Plagiochila spinulosa Prickly featherwort – to save and celebrate wild flowers, plants and Books fungi. They are the life support for all our wildlife Mosses and Liverworts of Britain and Ireland: A Field Guide 3 and their colour and character light up our by Ian Atherton, Sam Bosanquet and Mark Lawley (British landscapes. But without our help, this priceless Bryological Society, 2010). The best field guide. 2 natural heritage is in danger of being lost. The Liverwort Flora of the British Isles by Jean Paton (Harley 3 Books, 1999). An in-depth guide to liverwort identification, From the open spaces of our nature reserves to for more advanced bryologists. the corridors of government, we work nationally The Moss Flora of Britain and Ireland by A J E Smith and internationally to raise their profile, (2nd edition, Cambridge University Press, 2004). 1 celebrate their beauty and to protect their future. An in-depth guide to liverwort identification, for more advanced bryologists. 2 Mosses and Liverworts by Ron Porley and Nick Hodgetts Where wild plants lead (Collins New Naturalist series, Harper Collins, 2005). Habitat Often forming dense, mounded colonies on earth banks and around tree bases; also on boulders, rotten wood and Habitat In loose mats or dense cushions on trees and rock faces, often close to rivers and streams. Wildlife follows A highly readable account of moss and liverwort ecology occasionally on tree trunks. -
Ecosites and Communities of Forested Rangelands
Saskatchewan Rangeland Ecosystems Ecosites and Communities of Forested Rangelands Jeff Thorpe and Bob Godwin Saskatchewan Research Council 2008 Funding for this publication provided by Agriculture and Agri-Food Canada's Greencover Canada Program Ecosites and Communities of Forested Rangelands ACKNOWLEDGMENTS This project was coordinated by the Saskatchewan Forest Centre (SFC), with major funding support from Agriculture and Agri-food Canada’s Greencover Canada Program. Additional funding supporting was received from: • Saskatchewan Ministry of Agriculture (SA) • Forest Service Branch, Saskatchewan Ministry of Environment (SE) • Parks Service Branch, Saskatchewan Ministry of Tourism, Parks, Culture, and Sport (STPCS) • Saskatchewan Research Council (SRC) Todd Jorgenson (SA) and Al Foster (SA) helped with planning and coordination of the project, and Larry White (SFC) dealt with financial administration. Michael McLaughlan (SE), Rob Wright (SE) and Bill Houston (PFRA) provided access to vegetation plot data. SA staff, including Todd Jorgenson, Al Foster, and numerous summer students, and PFRA staff (Jenny Calow and Michelle Graham) contributed significant time to field data collection. A major part of the fieldwork was done by SRC subcontractors Wade Sumners, Chet Neufeld, and Randy Reddekopp. John Hudson (independent botanist) helped to identify plant collections. Charlene Hudym (SRC) prepared the report. Finally, we would like to acknowledge the advice and example provided by Gerry Ehlert and Barry Adams of Alberta Sustainable Resource -
<I>Sphagnum</I> Peat Mosses
ORIGINAL ARTICLE doi:10.1111/evo.12547 Evolution of niche preference in Sphagnum peat mosses Matthew G. Johnson,1,2,3 Gustaf Granath,4,5,6 Teemu Tahvanainen, 7 Remy Pouliot,8 Hans K. Stenøien,9 Line Rochefort,8 Hakan˚ Rydin,4 and A. Jonathan Shaw1 1Department of Biology, Duke University, Durham, North Carolina 27708 2Current Address: Chicago Botanic Garden, 1000 Lake Cook Road Glencoe, Illinois 60022 3E-mail: [email protected] 4Department of Plant Ecology and Evolution, Evolutionary Biology Centre, Uppsala University, Norbyvagen¨ 18D, SE-752 36, Uppsala, Sweden 5School of Geography and Earth Sciences, McMaster University, Hamilton, Ontario, Canada 6Department of Aquatic Sciences and Assessment, Swedish University of Agricultural Sciences, SE-750 07, Uppsala, Sweden 7Department of Biology, University of Eastern Finland, P.O. Box 111, 80101, Joensuu, Finland 8Department of Plant Sciences and Northern Research Center (CEN), Laval University Quebec, Canada 9Department of Natural History, Norwegian University of Science and Technology University Museum, Trondheim, Norway Received March 26, 2014 Accepted September 23, 2014 Peat mosses (Sphagnum)areecosystemengineers—speciesinborealpeatlandssimultaneouslycreateandinhabitnarrowhabitat preferences along two microhabitat gradients: an ionic gradient and a hydrological hummock–hollow gradient. In this article, we demonstrate the connections between microhabitat preference and phylogeny in Sphagnum.Usingadatasetof39speciesof Sphagnum,withan18-locusDNAalignmentandanecologicaldatasetencompassingthreelargepublishedstudies,wetested