picea rubens
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2022 ◽  
Vol 504 ◽  
pp. 119823
Author(s):  
C. Tattersall Smith ◽  
Christopher Preece ◽  
Inge Stupak ◽  
Russell D. Briggs ◽  
Bruna Barusco ◽  
...  

Author(s):  
Thibaut Capblancq ◽  
Helena Munson ◽  
John R. Butnor ◽  
Stephen R. Keller
Keyword(s):  

2021 ◽  
Vol 12 (1) ◽  
pp. 18-37
Author(s):  
Helen M. White ◽  
Lynn M. Resler ◽  
David Carroll

During the late 19th and early 20th centuries, intensive land use nearly eliminated red spruce (Picea rubens Sarg.) throughout portions of West Virginia (WV). Red spruce has been slow to regenerate on mountaintop heathland barrens surrounding Canaan Valley, West Virginia (WV), and little is known about the nature of encroachment. Using field surveys, geospatial data, and statistical modelling, the objectives were to 1) characterize and compare red spruce encroachment at two upland heath study areas in West Virginia (Bear Rocks and Cabin Mountain), 2) characterize percent cover of major ground cover types associated with red spruce regeneration sites in order to elucidate biotic interactions, and 3) model the biophysical correlates of red spruce encroachment using geospatial data and statistical modelling. Red spruce count was similar at both study areas, but there were substantially more seedlings and saplings at Cabin Mountain. Modelling revealed a positive relationship between red spruce count and rock cover and a negative relationship between red spruce and stand distance.


2020 ◽  
Vol 19 (10) ◽  
pp. 1101-1112
Author(s):  
David R. McMullin ◽  
Joey B. Tanney ◽  
Grace J. Daly ◽  
J. David Miller

2020 ◽  
Vol 13 (9) ◽  
pp. 2190-2205 ◽  
Author(s):  
Thibaut Capblancq ◽  
John R. Butnor ◽  
Sonia Deyoung ◽  
Ethan Thibault ◽  
Helena Munson ◽  
...  

2020 ◽  
Author(s):  
Cameron M. Stauder ◽  
Nicole M. Utano ◽  
Matt T. Kasson

AbstractThe Nectriaceae contains numerous canker pathogens. Due to scarcity of ascomata on many hosts, comprehensive surveys are lacking. Here we characterize the diversity of perithecia-producing nectriaceous fungi across the central Appalachians. Ten species from twelve hosts were recovered including a novel Corinectria sp. from Picea rubens. Neonectria ditissima and N. faginata were most abundant and associated with Fagus grandifolia with beech bark disease (BBD). N. ditissima was also recovered from additional cankered hardwoods, including previously unreported Acer spicatum, Ilex mucronata, and Sorbus americana. Cross-pathogenicity inoculations of N. ditissima confirmed susceptibility of Acer and Betula spp. Neonectria magnoliae was recovered from cankered Liriodendron tulipifera and Magnolia fraseri and pathogenicity on L. tulipifera was confirmed. Fusarium babinda was consistently recovered from beech with BBD, although its role remains unclear. This survey provides a contemporary snapshot of Nectriaceae diversity across the Appalachian Mountains. The following nomenclatural changes are proposed: Neonectria magnoliae comb. nov.


2019 ◽  
Vol 43 (1) ◽  
pp. 223-425 ◽  
Author(s):  
P.W. Crous ◽  
M.J. Wingfield ◽  
L. Lombard ◽  
F. Roets ◽  
W.J. Swart ◽  
...  

Novel species of fungi described in this study include those from various countries as follows: Antarctica , Apenidiella antarctica from permafrost, Cladosporium fildesense fromanunidentifiedmarinesponge. Argentina , Geastrum wrightii onhumusinmixedforest. Australia , Golovinomyces glandulariae on Glandularia aristigera, Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbia ficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.)on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max. British Virgin Isles , Lactifluus guanensis onsoil. Canada , Sorocybe oblongispora on resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma caverna fromcarbonatiteinKarstcave. Colombia , Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. Costa Rica, Psathyrella pivae onwood. Cyprus , Clavulina iris oncalcareoussubstrate. France , Chromosera ambigua and Clavulina iris var. occidentalis onsoil. French West Indies , Helminthosphaeria hispidissima ondeadwood. Guatemala , Talaromyces guatemalensis insoil. Malaysia , Neotracylla pini (incl. Tracyllales ord. nov. and Neotra- cylla gen. nov.)and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyrium viticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiae on Phoenix sp. Pakistan , Russula quercus-floribundae onforestfloor. Portugal , Trichoderma aestuarinum from salinewater. Russia , Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduouswoodorsoil. South Africa , Alloconiothyrium encephalarti, Phyllosticta encephalarticola and Neothyrostroma encephalarti (incl. Neothyrostroma gen. nov.)onleavesof Encephalartos sp., Chalara eucalypticola on leaf spots of Eucalyptus grandis× urophylla, Clypeosphaeria oleae on leaves of Olea capensis, Cylindrocladiella postalofficium on leaf litter of Sideroxylon inerme , Cylindromonium eugeniicola (incl. Cylindromonium gen. nov.)onleaflitterof Eugenia capensis , Cyphellophora goniomatis on leaves of Gonioma kamassi , Nothodactylaria nephrolepidis (incl. Nothodactylaria gen. nov. and Nothodactylariaceae fam. nov.)onleavesof Nephrolepis exaltata , Falcocladium eucalypti and Gyrothrix eucalypti on leaves of Eucalyptus sp., Gyrothrix oleae on leaves of Olea capensis subsp. macrocarpa , Harzia metro sideri on leaf litter of Metrosideros sp., Hippopotamyces phragmitis (incl. Hippopota- myces gen. nov.)onleavesof Phragmites australis , Lectera philenopterae on Philenoptera violacea , Leptosillia mayteni on leaves of Maytenus heterophylla , Lithohypha aloicola and Neoplatysporoides aloes on leaves of Aloe sp., Millesimomyces rhoicissi (incl. Millesimomyces gen. nov.) on leaves of Rhoicissus digitata , Neodevriesia strelitziicola on leaf litter of Strelitzia nicolai , Neokirramyces syzygii (incl. Neokirramyces gen. nov.)onleafspotsof


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