Works matching DE "EFFECT of carbon dioxide on plants"
Results: 487
CO effects on plant nutrient concentration depend on plant functional group and available nitrogen: a meta-analysis.
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- Plant Ecology, 2012, v. 213, n. 3, p. 505, doi. 10.1007/s11258-011-9998-8
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Carbon balance in a monospecific stand of an annual herb Chenopodium album at an elevated CO<sub>2</sub> concentration.
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- Plant Ecology, 2009, v. 203, n. 1, p. 33, doi. 10.1007/s11258-008-9502-2
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Stem respiration of Norway spruce trees under elevated CO concentration.
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- Biologia Plantarum, 2010, v. 54, n. 4, p. 773, doi. 10.1007/s10535-010-0140-x
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Sex-related and stage-dependent source-to-sink transition in Populus cathayana grown at elevated CO2 and elevated temperature.
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- Tree Physiology, 2012, v. 32, n. 11, p. 1325, doi. 10.1093/treephys/tps074
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Effects of predicted future and current atmospheric temperature and [CO<sub>2</sub>] and high and low soil moisture on gas exchange and growth of Pinus taeda seedlings at cool and warm sites in the species range.
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- Tree Physiology, 2012, v. 32, n. 7, p. 874, doi. 10.1093/treephys/tps051
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Transpiration modulates phosphorus acquisition in tropical tree seedlings.
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- Tree Physiology, 2011, v. 31, n. 8, p. 878, doi. 10.1093/treephys/tpr077
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Patchy stomatal behavior during midday depression of leaf CO2 exchange in tropical trees.
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- Tree Physiology, 2011, v. 31, n. 2, p. 160, doi. 10.1093/treephys/tpq102
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Elevated CO2 enhances leaf senescence during extreme drought in a temperate forest.
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- Tree Physiology, 2011, v. 31, n. 2, p. 117, doi. 10.1093/treephys/tpr002
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Seasonal fluctuations and temperature dependence in photosynthetic parameters and stomatal conductance at the leaf scale of Populus euphratica Oliv.
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- Tree Physiology, 2011, v. 31, n. 2, p. 178, doi. 10.1093/treephys/tpr005
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The bigger they are, the harder they fall: CO2 concentration and tree size affect drought tolerance.
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- Tree Physiology, 2011, v. 31, n. 2, p. 115, doi. 10.1093/treephys/tpr009
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Why do genotypes of Picea glauca differ in their growth response to elevated CO2?
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- Tree Physiology, 2011, v. 31, n. 1, p. 16, doi. 10.1093/treephys/tpq097
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Low moisture availability inhibits the enhancing effect of increased soil temperature on net photosynthesis of white birch (Betula papyrifera) seedlings grown under ambient and elevated carbon dioxide concentrations.
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- Tree Physiology, 2009, v. 29, n. 11, p. 1341, doi. 10.1093/treephys/tpp079
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Leaf and canopy conductance in aspen and aspen-birch forests under free-air enrichment of carbon dioxide and ozone.
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- Tree Physiology, 2009, v. 29, n. 11, p. 1367, doi. 10.1093/treephys/tpp070
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Interpretation of stem CO2 efflux measurements.
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- Tree Physiology, 2009, v. 29, n. 11, p. 1447, doi. 10.1093/treephys/tpp073
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Seasonal and long-term effects of CO2 and O3 on water loss in ponderosa pine and their interaction with climate and soil moisture.
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- Tree Physiology, 2009, v. 29, n. 11, p. 1381, doi. 10.1093/treephys/tpp071
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Wood CO2 efflux and foliar respiration for Eucalyptus in Hawaii and Brazil.
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- Tree Physiology, 2009, v. 29, n. 10, p. 1213, doi. 10.1093/treephys/tpp059
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Intra-annual dynamics of stem CO2 efflux in relation to cambial activity and xylem development in Pinus cembra.
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- Tree Physiology, 2009, v. 29, n. 5, p. 641, doi. 10.1093/treephys/tpp001
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Carbon dioxide exchange of buds and developing shoots of boreal Norway spruce exposed to elevated or ambient CO2 concentration and temperature in whole-tree chambers.
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- Tree Physiology, 2009, v. 29, n. 4, p. 461, doi. 10.1093/treephys/tpn047
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Do elevation of CO2 concentration and nitrogen fertilization alter storage and remobilization of carbon and nitrogen in pedunculate oak saplings?
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- Tree Physiology, 2008, v. 28, n. 11, p. 1729, doi. 10.1093/treephys/28.11.1729
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Size, shape and surface morphology of starch granules from Norway spruce needles revealed by transmission electron microscopy and atomic force microscopy: effects of elevated CO2 concentration.
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- Tree Physiology, 2008, v. 28, n. 10, p. 1593, doi. 10.1093/treephys/28.10.1593
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Sap flux in pure aspen and mixed aspen–birch forests exposed to elevated concentrations of carbon dioxide and ozone.
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- Tree Physiology, 2008, v. 28, n. 8, p. 1231, doi. 10.1093/treephys/28.8.1231
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Impact of needle age on the response of respiration in Scots pine to long-term elevation of carbon dioxide concentration and temperature.
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- Tree Physiology, 2002, v. 22, n. 17, p. 1241, doi. 10.1093/treephys/22.17.1241
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Carbon acquisition and water use in a northern Utah Juniperus osteosperma (Utah juniper) population.
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- Tree Physiology, 2002, v. 22, n. 17, p. 1221, doi. 10.1093/treephys/22.17.1221
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Diameter growth of Scots pine (Pinus sylvestris) trees grown at elevated temperature and carbon dioxide concentration under boreal conditions.
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- Tree Physiology, 2002, v. 22, n. 14, p. 963, doi. 10.1093/treephys/22.14.963
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Derivation of stem taper from the pipe theory in a carbon balance framework.
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- Tree Physiology, 2002, v. 22, n. 13, p. 891, doi. 10.1093/treephys/22.13.891
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Gas exchange, biomass, whole-plant water-use efficiency and water uptake of peach (Prunus persica) seedlings in response to elevated carbon dioxide concentration and water availability.
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- Tree Physiology, 2002, v. 22, n. 10, p. 699, doi. 10.1093/treephys/22.10.699
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Responses of deciduous broadleaf trees to defoliation in a CO2 enriched atmosphere.
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- Tree Physiology, 2002, v. 22, n. 7, p. 435, doi. 10.1093/treephys/22.7.435
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Growth rate and survivorship of drought: CO2 effects on the presumed tradeoff in seedlings of five woody legumes.
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- Tree Physiology, 2002, v. 22, n. 6, p. 383, doi. 10.1093/treephys/22.6.383
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Carbon dioxide and water vapor exchange by young and old ponderosa pine ecosystems during a dry summer.
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- Tree Physiology, 2001, v. 21, n. 5, p. 299, doi. 10.1093/treephys/21.5.299
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Effects of CO2 enrichment on the photosynthetic light response of sun and shade leaves of canopy sweetgum trees (Liquidambar styraciflua) in a forest ecosystem.
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- Tree Physiology, 1999, v. 19, n. 12, p. 779, doi. 10.1093/treephys/19.12.779
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Long-term effects of elevated carbon dioxide concentration and provenance on four clones of Sitka spruce (Picea sitchensis). I. Plant growth, allocation and ontogeny.
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- Tree Physiology, 1999, v. 19, n. 12, p. 799, doi. 10.1093/treephys/19.12.799
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Influence of environmental and plant factors on canopy photosynthesis and transpiration of apple trees.
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- Tree Physiology, 1997, v. 17, n. 10, p. 637, doi. 10.1093/treephys/17.10.637
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Effect of elevated carbon dioxide concentration and root restriction on net photosynthesis, water relations and foliar carbohydrate status of loblolly pine seedlings.
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- Tree Physiology, 1997, v. 17, n. 10, p. 655, doi. 10.1093/treephys/17.10.655
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Leaf conductance and CO2 assimilation of Larix gmelinii growing in an eastern Siberian boreal forest.
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- Tree Physiology, 1997, v. 17, n. 10, p. 607, doi. 10.1093/treephys/17.10.607
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Effects of dessication on post-planting stress in bare-root Corsican pine seedlings.
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- Tree Physiology, 1997, v. 17, n. 7, p. 429, doi. 10.1093/treephys/17.7.429
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Carbon dioxide gas exchange of cembran pine (Pinus cembra) at the alpine timberline during winter.
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- Tree Physiology, 1997, v. 17, n. 7, p. 473, doi. 10.1093/treephys/17.7.473
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Effect of measurement CO2 concentration on sugar maple root respiration.
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- Tree Physiology, 1997, v. 17, n. 7, p. 421, doi. 10.1093/treephys/17.7.421
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Effects of elevated CO2 on chloroplast components, gas exchange and growth of oak and cherry.
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- Tree Physiology, 1997, v. 17, n. 5, p. 319, doi. 10.1093/treephys/17.5.319
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Elevated atmospheric CO2 concentration changes ectomycorrhizal morphotype assemblages in Betula papyrifera.
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- Tree Physiology, 1997, v. 17, n. 5, p. 347, doi. 10.1093/treephys/17.5.347
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Leaf physiology, production, water use, and nitrogen dynamics of the grassland invader Acacia smallii at elevated CO2 concentrations.
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- Tree Physiology, 1997, v. 17, n. 2, p. 89, doi. 10.1093/treephys/17.2.89
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Effect of mineral nutrition content on oxygen exchange and chlorophyll a fluorescence in needles of Norway spruce.
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- Tree Physiology, 1997, v. 17, n. 4, p. 221, doi. 10.1093/treephys/17.4.221
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Carbon dioxide enrichment improves growth, water relations and survival of droughted honey mesquite (Prosopis glandulosa) seedlings.
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- Tree Physiology, 1996, v. 16, n. 10, p. 817, doi. 10.1093/treephys/16.10.817
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Growth and carbon accumulation in root systems of Pinus taeda and Pinus ponderosa seedlings as affected by varying CO2, temperature and nitrogen.
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- Tree Physiology, 1996, v. 16, n. 7, p. 635, doi. 10.1093/treephys/16.7.635
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Sensitive indicators of Stipa bungeana response to precipitation under ambient and elevated CO concentration.
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- International Journal of Biometeorology, 2018, v. 62, n. 2, p. 141, doi. 10.1007/s00484-017-1434-x
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Response of Cassava canopy to mid-day pseudo sunrise induced by solar eclipse.
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- International Journal of Biometeorology, 2013, v. 57, n. 4, p. 645, doi. 10.1007/s00484-012-0576-0
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Elevated CO<sub>2</sub> further lengthens growing season under warming conditions.
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- Nature, 2014, v. 510, n. 7504, p. 259, doi. 10.1038/nature13207
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C<sub>4</sub> grasses prosper as carbon dioxide eliminates desiccation in warmed semi-arid grassland.
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- Nature, 2011, v. 476, n. 7359, p. 202, doi. 10.1038/nature10274
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Elevated CO 2 may reduce arsenic accumulation in diverse ecotypes of Arabidopsis thaliana.
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- Journal of Plant Nutrition, 2018, v. 41, n. 5, p. 645, doi. 10.1080/01904167.2017.1415352
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Elevated CO 2 Improves Growth and Phosphorus Utilization Efficiency in Cereal Species Under Sub-Optimal Phosphorus Supply.
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- Journal of Plant Nutrition, 2015, v. 38, n. 8, p. 1196, doi. 10.1080/01904167.2014.983116
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Microbially mediated CH<sub>4</sub> consumption and N<sub>2</sub>O emission is affected by elevated CO<sub>2</sub>, soil water content, and composition of semi-arid grassland species.
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- Plant & Soil, 2010, v. 329, n. 1/2, p. 269, doi. 10.1007/s11104-009-0152-5
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