Responding to the predicted shift in climate envelope jack pine, ( Pinus banksiana Lamb.) might migrate 10° northward between 2071 and 2100 and will be exposed to a different photoperiod regime. Successful migration of the species might depend on the initial acclimating capability to the conditions of new location. The impacts of elevated carbon dioxide concentration [CO 2 ], soil temperature and photoperiod on the phenological traits, growth and biomass responses in jack pine seedlings were investigated. Seedlings were grown in greenhouses under two [CO 2 ] (400 and 950 μmol • mol -1 ), two soil temperatures (ambient soil temperature at seed origin and 5°C warmer) and three photoperiod regimes (photoperiods at seed origin, 5° north of the seed origin and 10° north of the seed origin). Budburst and bud setting time were recorded and the seedling height (Ht), root collar diameter (RCD), root biomass, stem biomass and leaf biomass were measured after six months of treatment. It was observed that under elevated [CO 2 ], ambient T soil and photoperiods associated with 10° northward migrations budburstis advanced by 10 days. Photoperiods toward north significantly prolonged the bud setting time. However, tri-factor interactive effect on bud set was not statistically significant. Elevated [CO 2 ] significantly (P < 0.05) increased the RCD, volume of the seedlings and total biomass and longer growing season photoperiods towards north significantly increased the seedling heights. Though elevated [CO 2 ] significantly increased the projected leaf area, it had no significant effect on specific leaf area. Elevated [CO 2 ] significantly reduced the shoot to root ratio, which indicated higher biomass allocation in roots under elevated [CO 2 ]. However, all these growth and biomass responses were statistically insignificant under tri-factor interactive effects. The results suggest that climate change induced northward migration will not affect the growth of jack pine. However, a long distance migration (e.g. 10° north) will expose the species to late-spring frost damage.
Soolanayakanahally, R.Y., Guy, R.D., Silim, S.N. and Song, M. (2013) Timing of Photoperiodic Competency Causes Phenological Mismatch in Balsam Poplar (Populus balsamifera L.). Plant, Cell and Environment, 36, 116-127. http://dx.doi.org/10.1111/j.1365-3040.2012.02560.x
Aitken, S.N., Yeaman, S., Holliday, J.A., Wang, T.L. and Curtis-McLane, S. (2008) Adaptation, Migration or Extirpation: Climate Change Outcomes for Tree Populations. Evolutionary Applications, 1, 95-111. http://dx.doi.org/10.1111/j.1752-4571.2007.00013.x
Bunnell, F.L. and Kremsater, L.L. (2012) Migrating Like a Herd of Cats: Climate Change and Emerging Forests in British Columbia. Journal of Ecosystems and Management, 13, 27-50.
Johnston, M.H., Campagna, M., Gray, P.A., Kope, H.H., Loo, J.A., Ogden, A.E., O’Neill, G.A., Price, D.T. and Williamson, T.B. (2009) Vulnerability of Canada’s Tree Species to Climate Change and Management Options for Adaptation: An Overview for Policy Makers and Practitioners. Canadian Council of Forest Ministers. Northern Forestry Centre, 44.
Huang, J.G., Bergeron, Y., Denneler, B., Berninger, F. and Tardif, J. (2007) Response of Forest Trees to Increased Atmospheric CO2. Critical Reviews in Plant Sciences, 26, 265-283. http://dx.doi.org/10.1080/07352680701626978
Lambers, H., Chapin III, F.S. and Thijs, L.P. (2008) Plant Physiological Ecology. 2nd Edition, Springer, New York, 604 p.
Lukac, M., Calfapietra, C., Lagomarsino, A. and Loreto, F. (2010) Global Climate Change and Tree Nutrition: Effects of Elevated CO2 and Temperature. Tree Physiology, 30, 1209-1220. http://dx.doi.org/10.1093/treephys/tpq040
Ainsworth, E.A. and Long, S.P. (2005) What Have We Learned from 15 Years of Free-Air CO2 Enrichment (FACE)? A Meta-Analytic Review of the Responses of Photosynthesis, Canopy Properties and Plant Production to Rising CO2. New Phytologist, 165, 351-372. http://dx.doi.org/10.1111/j.1469-8137.2004.01224.x
Curtis, P.S. and Wang, X. (1998) A Meta-Analysis of Elevated CO2 Effects on Woody Plant Mass, Form, and Physiology. Oecologia, 113, 299-313. http://dx.doi.org/10.1007/s004420050381
Idso, K.E. and Edso, S.B. (1994) Plant Responses to Atmospheric CO2 Enrichment in the Face of Environmental Constraints: A Review of the Past 10 Years’ Research. Agricultural and Forest Meteorology, 69, 153-203. http://dx.doi.org/10.1016/0168-1923(94)90025-6
Marfo, J. and Dang, Q.L. (2009) Interactive Effects of Carbon Dioxide Concentration and Light on the Morphological and Biomass Characteristics of Black Spruce Seedlings. Botany, 87, 67-77. http://dx.doi.org/10.1139/B08-114
Norby, R.J., Wullschleger, S.D., Gunderson, C.A., Johnson, D.W. and Ceulemans, R. (1999) Tree Responses to Rising CO2 in Field Experiments: Implication for Future Forest. Plant, Cell and Environment, 22, 683-714. http://dx.doi.org/10.1046/j.1365-3040.1999.00391.x
Pregitzer, K.S., King, J.S., Andrew, J.B. and Brown, E. (2000) Responses of Tree Fine Roots to Temperature. New Phytologist, 147, 105-115. http://dx.doi.org/10.1046/j.1469-8137.2000.00689.x
Eamus, D. and Jarvis, P.G. (1989) The Direct Effects of Increase in the Global Atmospheric CO2 Concentration on Natural and Commercial Temperate Trees and Forests. Advances in Ecological Research, 19, 1-55. http://dx.doi.org/10.1016/S0065-2504(08)60156-7
Koch, K.E., Jones, P.H., Avigne, W.T. and Allen, L.H. (1986) Growth and Dry Matter Partitioning and Diurnal Activities of RuBP Carboxylase in Citrus Seedlings Maintained at Two Levels of CO2. Physiologia Plantarum, 67, 477-484. http://dx.doi.org/10.1111/j.1399-3054.1986.tb05766.x
Norby, R.J. and O’Neill, E.G. (1989) Growth Dynamics and Water Use of Seedlings of Quercus alba L. in CO2-Enriched Atmospheres. New Phytologist, 111, 491-500. http://dx.doi.org/10.1111/j.1469-8137.1989.tb00712.x
Pettersson, R., McDonald, A.J.S. and Stadenberg, I. (1993) Response of Small Birch Plants (Betula pendula Roth.) to Elevated CO2 and Nitrogen Supply. Plant, Cell & Environment, 16, 1115-1121. http://dx.doi.org/10.1111/j.1365-3040.1996.tb02069.x
Samuelson, L.J. and Seiler, J.R. (1993) Interactive Role of Elevated CO2, Nutrient Limitations, and Water Stress in the Growth Responses of Red Spruce Seedlings. Forest Science, 39, 348-358.
Rogers, H.H., Runion, G.B. and Krupa, S.V. (1994) Plant Responses to Atmospheric CO2 Enrichment with Emphasis on Roots and the Rhizosphere. Environmental Pollution, 83, 155-189. http://dx.doi.org/10.1016/0269-7491(94)90034-5
Tingey, D.T., Phillips, D.L. and Johnson, M.G. (2000) Elevated CO2 and Conifer Roots: Effects on Growth, Life Span and Turnover. New Phytologist, 147, 87-103. http://dx.doi.org/10.1046/j.1469-8137.2000.00684.x
Day, F.P., Weber, E.P., Hinckle, C.R. and Drake, B.G. (1996) Effects of Elevated Atmospheric CO2 on Fine Root Length and Distribution in an Oak-Palmetto Scrub Ecosystem in Central Florida. Global Change Biology, 2, 143-148. http://dx.doi.org/10.1111/j.1365-2486.1996.tb00059.x
Janssens, I.A., Crookshanks, M., Taylor, G. and Ceulemans, R. (1998) Elevated CO2 Increases Fine Root Production, Respiration, Rhizosphere Respiration and Soil CO2 Efflux in Scots Pine Seedlings. Global Change Biology, 4, 871-878. http://dx.doi.org/10.1046/j.1365-2486.1998.00199.x
Bigras, F.J. and Bertrand, A. (2006) Responses of Piceamariana to Elevated CO2 Concentration during Growth, Cold Hardening and Dehardening: Phenology, Cold Tolerance, Photosynthesis and Growth. Tree Physiology, 26, 875-888. http://dx.doi.org/10.1093/treephys/26.7.875
Ceulemans, R., Jiang, X.N. and Shao, B.Y. (1995) Effects of Elevated Atmospheric CO2 on Growth, Biomass Production and Nitrogen Allocation of Two Populus Clones. Journal of Biogeography, 22, 261-268. http://dx.doi.org/10.2307/2845920
Jach, M.E. and Ceulemans, R. (1999) Effects of Elevated Atmospheric CO2 on Phenology, Growth and Crown Structure of Scots Pine (Pinus sylvestris) Seedlings after Two Years of Exposure in the Field. Tree Physiology, 19, 289-300. http://dx.doi.org/10.1093/treephys/19.4-5.289
Murray, M.B., Cannell, M.G.R. and Smith, R.I. (1989) Date of Bud Burst of Fifteen Tree Species in Britain Following Climate Warming. Journal of Applied Ecology, 26, 693-700. http://dx.doi.org/10.2307/2404093
Heninger, R.L. and White, D.P. (1974) Tree Seedling Growth at Different Soil Temperatures. Forest Science, 20, 363-367.
Lyford, W.H. and Wilson, B.F. (1966) Controlled Growth of Forest Tree Roots: Technique and Application. Harvard Forest Paper 16, p. 12.
Alvarez-Uria, P. and Korner, C. (2007) Low Temperature Limits of Root Growth in Deciduous and Evergreen Temperate Tree Species. Functional Ecology, 21, 211-218. http://dx.doi.org/10.1111/j.1365-2435.2007.01231.x
Cai, T.B. and Dang, Q.L. (2002) Effects of Soil Temperature on Parameters of a Coupled Photosynthesis-Stomatal Conductance Model. Tree Physiology, 22, 819-828. http://dx.doi.org/10.1093/treephys/22.12.819
Camm, E.L. and Harper, G.J. (1991) Temporal Variations in Cold Sensitivity of Root Growth in Cold-Stored White Spruce Seedlings. Tree Physiology, 9, 425-431. http://dx.doi.org/10.1093/treephys/9.3.425
Dang, Q.L. and Cheng, S. (2004) Effects of Soil Temperature on Ecophysiological Traits in Seedlings of Four Boreal Tree Species. Forest Ecology and Management, 194, 379-387. http://dx.doi.org/10.1016/j.foreco.2004.03.004
Landhausser, S.M., DesRochers, A. and Lieffers, V.J. (2001) A Comparison of Growth and Physiology in Picea glauca and Populus tremuloides at Different Soil Temperatures. Canadian Journal of Forest Research, 31, 1922-1929.
Stathers, R.J. and Spittlehouse, D.L. (1990) Forest Soil Temperature Manual. FRDA Report No. 130, British Columbia Ministry of Forests, Victoria.
Grossnickle, S.C. (2000) Ecophysiology of Northern Spruce Species: The performance of Planted Seedlings. NRC Research Press, Ottawa, 409.
Peng, Y.Y. and Dang, Q.L. (2003) Effects of Soil Temperature on Biomass Production and Allocation in Seedlings of Four Boreal Tree Species. Forest Ecology and Management, 180, 1-9. http://dx.doi.org/10.1016/S0378-1127(02)00486-3
Tierney, G., Fahey, T., Groffman, P., Hardy, J., Fitzhugh, R. and Driscoll, C. (2001) Soil Freezing Alters Fine Root Dynamics in A Northern Hardwood Forest. Biogeochemistry, 56, 175-190. http://dx.doi.org/10.1023/A:1013072519889
Ambebe, T.F., Dang, Q.L. and Li, J. (2010) Low Soil Temperature Inhibits the Effects of High Nutrient Supply on Photosynthetic Response to Elevated Carbon Dioxide Concentration in White Birch Seedlings. Tree Physiology, 30, 234-243. http://dx.doi.org/10.1093/treephys/tpp109
Domisch, T., Finer, L., Lehto, T. and Smolander, A. (2002) Effect of Soil Temperature on Nutrient Allocation and Mycorrhizas in Scots Pine Seedlings. Plant and Soil, 239, 173-185. http://dx.doi.org/10.1023/A:1015037127126
Haussling, C.A., Jorn, C.A., Lehmbecker, G., Hecht-Buchholz, C. and Marschner, H. (1988) Ion and Water Uptake in Relation to Root Development in Norway Spruce (Picea abies [L.] Karst.). Journal of Plant Physiology, 133, 486-491. http://dx.doi.org/10.1016/S0176-1617(88)80042-7
Campbell, R.K. and Sugano, A.I. (1975) Phenology of Bud Burst in Douglas-Fir Related to Provenance, Photoperiod, Chilling, and Flushing Temperature. International Journal of Plant Sciences, 136, 290-298. http://dx.doi.org/10.1086/336817
Campbell, R.K. (1979) Genecology of Douglas-Fir in a Watershed in the Oregon Cascades. Ecology, 60, 1036-1050. http://dx.doi.org/10.2307/1936871
Weiser, C.J. (1970) Cold Resistance and Injury in Woody Plants. Science, 169, 1269-1278. http://dx.doi.org/10.1126/science.169.3952.1269
Hanninen, H. (2006) Climate Warming and the Risk of Frost Damage to Boreal Forest Trees: Identification of Critical Ecophysiological Traits. Tree Physiology, 26, 889-898. http://dx.doi.org/10.1093/treephys/26.7.889
Thomas, B. and Vince-Prue, D. (1997) Photoperiodism in Plants. 2nd Edition, Academic Press, San Diego, 428.
Colombo, S.J., Zhao, S.Y. and Blumwald, E. (1995) Frost Hardiness Gradients in Shoots and Roots of Picea mariana Seedlings. Scandinavian Journal of Forest Research, 10, 32-36. http://dx.doi.org/10.1080/02827589509382864
Fracheboud, Y., Luquez, V., Bjorkén, L., Sjodin, A., Tuominen, H. and Jansson, S. (2009) The Control of Autumn Senescence in European Aspens. Plant Physiology, 149, 1982-1991. http://dx.doi.org/10.1104/pp.108.133249
Curtis, P.S., Vogel, C.S., Wang, X., Pregistzer, K.S., Zak, D.R., Lussenhop, J., Kubiske, M. and Teeri, J.A. (2000) Gas Exchange, Leaf Nitrogen, and Growth Efficiency of Populus tremuloides in a CO2-Enriched Atmosphere. Ecological Applications, 10, 3-17.
Nowak, R.S., Ellsworth, D.S. and Smith, S.D. (2004) Functional Responses of Plants to Elevated Atmospheric CO2—Do Photosynthetic and Productivity Data from FACE Experiments Support Early Predictions? New Phytologist, 162, 253-280. http://dx.doi.org/10.1111/j.1469-8137.2004.01033.x
Allen, S.G., Idso, S.B. and Kimball, B.A. (1990) Interactive Effects of CO2 and Environment on Net Photosynthesis of Water-Lily. Agriculture, Ecosystems & Environment, 30, 81-88. http://dx.doi.org/10.1016/0167-8809(90)90185-G
Mishra, R.S., Abdin, M.Z. and Uprety, D.C. (1999) Interactive Effects of Elevated CO2 and Moisture Stress on the Photosynthesis, Water Relation and Growth of Brassica Species. Journal of Agronomy & Crop Science, 182, 223-229. http://dx.doi.org/10.1046/j.1439-037x.1999.00294.x
Robredo, A., Pérez-López, U., Sainz, H., de la Maza, B., González-Moro, M.L., Mena-Petite, A. and Munoz-Rueda, A. (2007) Elevated CO2 Alleviates the Impact of Drought on Barley Improving Water Status by Lowering Stomatal Conductance and Delaying Its Effects on Photosynthesis. Environmental and Experimental Botany, 59, 252-263. http://dx.doi.org/10.1016/j.envexpbot.2006.01.001
Zebian, K.J. and Reekie, E.G. (1998) The Interactive Effects of Atmospheric Carbon Dioxide and Light on Stem Elongation in Seedlings of Four Species. Annals of Botany, 81, 185-193. http://dx.doi.org/10.1006/anbo.1997.0528
Cantin, D., Tremblay, M.F., Lechowicz, M.J. and Potvin, C. (1997) Effects of CO2 Enrichment, Elevated Temperature, and Nitrogen Availability on the Growth and Gas Exchange of Different Families of Jack Pine Seedlings. Canadian Journal of Forest Research, 27, 510-520.
DeLucia, E.H. and Smith, W.K. (1987) Air and Soil Temperature Limitations on Photosynthesis in Engelmann Spruce during Summer. Canadian Journal of Forest Research, 17, 527-533. http://dx.doi.org/10.1139/x87-088
Fraser, D.A. (1962) Growth of Spruce Seedlings under Long Photoperiods. Canada Department of Forestry, Forest Research Branch, Technical Note No. 114.
Li, J., Dang, Q.L. and Man, R. (2015) Photoperiod and Nitrogen Supply Limit the Scope of Northward Migration and Seed Transfer of Black Spruce in a Future Climate Associated with Doubled Atmospheric CO2 Concentration. American Journal of Plant Sciences, 6, 189-200. http://dx.doi.org/10.4236/ajps.2015.61022
Way, D.A. and Sage, R.F. (2008) Thermal Acclimation of Photosynthesis in Black Spruce [Picea mariana (Mill.) B.S.P.]. Plant, Cell and Environment, 31, 1250-1262. http://dx.doi.org/10.1111/j.1365-3040.2008.01842.x
Way, D.A. and Sage, R.F. (2008) Elevated Growth Temperatures Reduce the Carbon Gain of Black Spruce [Picea mariana (Mill.) B.S.P.]. Global Change Biology, 14, 624-636. http://dx.doi.org/10.1111/j.1365-2486.2007.01513.x
Fowells, H.A. (1965) Silvics of Forest Trees of the United States. US Department of Agriculture, Agriculture Handbook No. 271.
Forestry Canada (1992) Selected Forestry Statistics Canada 1991. Forestry Canada, Policy and Economics Directorate, Ottawa. Information Report E-X-46, 231 p.
OMNR (1991) Statistics 1989-1990. Queen’s Printer for Ontario, Toronto, 106 p.
McKenney, D.W., Pedlar, J.H., Lawrence, K.E.V.I., Campbell, K. and Hutchinson, M.F. (2007) Potential Impacts of Climate Change on the Distribution of North American Trees. BioScience, 57, 939-948. http://dx.doi.org/10.1641/B571106
McKenney, D.W., Pedlar, J.H., Rood, R.B. and Price, D.A.V.I. (2011) Revisiting Projected Shifts in the Climate Envelopes of North American Trees Using Updated General Circulation Models. Global Change Biology, 17, 2720-2730. http://dx.doi.org/10.1111/j.1365-2486.2011.02413.x
Pearson, R.G. and Dawson, T.P. (2003) Predicting the Impacts of Climate Change on the Distribution of Species: Are Bioclimate Envelope Models Useful? Global Ecology and Biogeography, 12, 361-371. http://dx.doi.org/10.1046/j.1466-822X.2003.00042.x
Tjoelker, M.G., Oleksyn, J. and Reich, P.B. (1998) Seedlings of Five Boreal Tree Species Differ in Acclimation of Net Photosynthesis to Elevated CO2 and Temperature. Tree Physiology, 18, 715-726. http://dx.doi.org/10.1093/treephys/18.11.715
Cheng, S., Dang, Q.L. and Cai, T.B. (2000) A Soil Temperature Control System for Ecological Research in Greenhouses. Journal of Forest Research, 5, 205-208. http://dx.doi.org/10.1007/BF02762403
Scarratt, J.B. (1986) An Evaluation of Some Commercial Soluble Fertilizers for Culture of Jack Pine Container Stock. Canadian Forestry Service, Great Lakes Forestry Centre, Sault Ste. Marie, Ontario, Information Report O-X-377, 21 p.
van den Driessche, R. (1992) Absolute and Relative Growth of Douglas-Fir Seedlings of Different Sizes. Tree Physiology, 10, 141-152. http://dx.doi.org/10.1093/treephys/10.2.141
R Core Team (2015) R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org/
Basler, D. and Korner, C. (2012) Photoperiod Sensitivity of Bud Burst in 14 Temperate Forest Tree Species. Agricultural and Forest Meteorology, 165, 73-81. http://dx.doi.org/10.1016/j.agrformet.2012.06.001
Heide, O.M. (1993) Daylength and Thermal Time Responses of Bud Burst during Dormancy Release in Some Northern Deciduous Trees. Physiologia Plantarum, 88, 531-540. http://dx.doi.org/10.1111/j.1399-3054.1993.tb01368.x
Heide, O.M. (1993) Dormancy Release in Beech Buds (Fagus sylvatica) Requires Both Chilling and Long Days. Physiologia Plantarum, 89, 187-191. http://dx.doi.org/10.1111/j.1399-3054.1993.tb01804.x
Korner, C. and Basler, D. (2010) Phenology under Global Warming. Science, 327, 1461-1462. http://dx.doi.org/10.1126/science.1186473
Laube, J., Sparks, T.H., Estrella, N., Hofler, J., Ankerst, D.P. and Menzel, A. (2014) Chilling Outweighs Photoperiod in Preventing Precocious Spring Development. Global Change Biology, 20, 170-182. http://dx.doi.org/10.1111/gcb.12360
Myking, T. and Heide, O.M. (1995) Dormancy Release and Chilling Requirement of Buds of Latitudinal Ecotypes of Betula pendula and B. pubescens. Tree Physiology, 15, 697-704. http://dx.doi.org/10.1093/treephys/15.11.697
Partanen, J., Koski, V. and Hanninen, H. (1998) Effects of Photoperiod and Temperature on the Timing of Bud Burst in Norway Spruce (Picea abies). Tree Physiology, 18, 811-816. http://dx.doi.org/10.1093/treephys/18.12.811
Zohner, C.M. and Renner, S.S. (2014) Common Garden Comparison of the Leaf-Out Phenology of Woody Species from Different Native Climates, Combined with Herbarium Records Forecasts Long-Term Change. Ecology Letters, 17, 1016-1025. http://dx.doi.org/10.1111/ele.12308
Zohner, C.M. and Renner, S.S. (2015) Perception of Photoperiod in Individual Buds of Mature Trees Regulates Leaf-Out. New Phytologist, 208, 1023-1030. http://dx.doi.org/10.1111/nph.13510
Jach, M.E., Ceulemans, R. and Murray, M.B. (2001) Impacts of Greenhouse Gases on the Phenology of Forest Trees. In: Karnosky, D.F., Ceulemans, R., Scarascia-Mugnozza, G.E. and Innes, J.L., Eds., The Impact of Carbon Dioxide and Other Greenhouse Gases on Forest Ecosystems, CABI Publishing, CAB International, Wallingford, Oxford, 193-235. http://dx.doi.org/10.1079/9780851995519.0193
Slaney, M., Wallin, G., Medhurst, J. and Linder, S. (2007) Impact of Elevated Carbon Dioxide Concentration and Temperature on Bud Burst and Shoot Growth of Boreal Norway Spruce. Tree Physiology, 27, 301-312. http://dx.doi.org/10.1093/treephys/27.2.301
Apple, M.E., Lucash, M.S., Olszyk, D.M. and Tingey, D.T. (1998) Morphogenesis of Douglas Fir Buds Is Altered at Elevated Temperature but Not at Elevated CO2. Environmental and Experimental Botany, 40, 159-172. http://dx.doi.org/10.1016/S0098-8472(98)00031-8
Olszyk, D., Wise, C., VanEss, E., Apple, M. and Tingey, D. (1998) Phenology and Growth of Shoots, Needles, and Buds of Douglas-Fir Seedlings with Elevated CO2 and (or) Temperature. Canadian Journal of Botany, 76, 1991-2001.
Roberntz, P. (1999) Effects of Long-Term CO2 Enrichment and Nutrient Availability in Norway Spruce. I. Phenology and Morphology of Branches. Trees, 18, 188-198. http://dx.doi.org/10.1007/pl00009750
Bergh, J. and Linder, S. (1999) Effects of Soil Warming during Spring on Photosynthetic Recovery in Boreal Norway Spruce Stands. Global Change Biology, 5, 245-253. http://dx.doi.org/10.1046/j.1365-2486.1999.00205.x
Domisch, T., Finer, L. and Lehto, T. (2001) Effects of Soil Temperature on Biomass and Carbohydrate Allocation in Scots Pine (Pinus sylvestris) Seedlings at the Beginning of the Growing Season. Tree Physiology, 21, 465-472. http://dx.doi.org/10.1093/treephys/21.7.465
Vapaavuori, E.M., Rikala, R. and Ryyppo, A. (1992) Effects of Root Temperature on Growth and Photosynthesis in Conifer Seedlings during Shoot Elongation. Tree Physiology, 10, 217-230. http://dx.doi.org/10.1093/treephys/10.3.217
Lyr, H. and Garbe, V. (1995) Influence of Root Temperature on Growth of Pinus sylvestris, Fagus sylvatica, Tilia cordata and Quercus robur. Trees, 9, 220-223. http://dx.doi.org/10.1007/BF00195276
Basler, D. and Korner, C. (2014) Photoperiod and Temperature Responses of Bud Swelling and Bud Burst in Four Temperate Forest Tree Species. Tree Physiology, 34, 377-388. http://dx.doi.org/10.1093/treephys/tpu021
Hanninen, H. (1990) Modelling Bud Dormancy Release in Trees from Cool and Temperate Regions. Acta Forestalia Fennica, 213, 1-47.
Dalen, L.S. (1998) Elevated CO2 and Development of Frost Hardiness in Norway Spruce (Picea abies (L.) Karst). Thesis, Agricultural University of Norway.
Centritto, M., Lee, H.S.J. and Jarvis, P.G. (1999) Long-Term Effects of Elevated Carbon Dioxide Concentration and Provenance on Four Clones of Sitka Spruce (Picea sitchensis). I. Plant Growth, Allocation and Ontogeny. Tree Physiology, 19, 799-806. http://dx.doi.org/10.1093/treephys/19.12.799
Murray, M.B., Smith, R.I., Leith, I.D., Fowler, D., Lee, H.S.J., Friend, A.D. and Jarvis, P.G. (1994) Effects of Elevated CO2, Nutrition and Climatic Warming on Bud Phenology in Sitka Spruce (Picea sitchensis) and Their Impact on the Risk of Frost Damage. Tree Physiology, 14, 691-706. http://dx.doi.org/10.1093/treephys/14.7-8-9.691
Surano, K.A., Daley, P.F., Houpis, J.L.J., Shinn, J.H., Helms, J.A., Palassou, R.J. and Costella, M.P. (1986) Growth and Physiological Responses of Pinus ponderosa Dougl ex P. Laws. to Long-Term Elevated CO2 Concentrations. Tree Physiology, 2, 243-259. http://dx.doi.org/10.1093/treephys/2.1-2-3.243
Guehl, J.M., Picon, C., Aussenac, G. and Gross, P. (1994) Interactive Effects of Elevated CO2 and Soil Drought on Growth and Transpiration Efficiency and Its Determinants in Two European Forest Tree Species. Tree Physiology, 14, 707-724. http://dx.doi.org/10.1093/treephys/14.7-8-9.707
Johnsen, K.H. and Seiler, J.R. (1996) Growth, Shoot Phenology and Physiology of Diverse Seed Sources of Black Spruce: I. Seedling Responses to Varied Atmospheric CO2 Concentrations and Photoperiods. Tree Physiology, 16, 367-373. http://dx.doi.org/10.1093/treephys/16.3.367
DeLucia, E.H. and Thomas, R.B. (2000) Photosynthetic Responses to CO2 Enrichment of Four Hardwood Species in a Forest Understory. Oecologia, 122, 11-19. http://dx.doi.org/10.1007/PL00008827
Zhang, S. and Dang, Q.L. (2006) Effects of Carbon Dioxide and Nutrition on Photosynthetic Functions of White Birch Seedlings. Tree Physiology, 26, 1457-1467. http://dx.doi.org/10.1093/treephys/26.11.1457
Pushnik, J.C., Demaree, R.S., Houpis, J.L.J., Flory, W.B., Bauer, S.M. and Anderson, P.D. (1995) The Effect of Elevated Carbon Dioxide on a Sierra-Nevadan Dominant Species: Pinus ponderosa. Journal of Biogeography, 22, 249-254. http://dx.doi.org/10.2307/2845918
Ambebe, T.F., Danyagri, G. and Dang, Q.L. (2013) Low Soil Temperature Inhibits the Stimulatory Effect of Elevated [CO2] on Height and Biomass Accumulation of White Birch Seedlings Grown under Three Non-Limiting Phosphorus Conditions. Nordic Journal of Botany, 31, 239-246. http://dx.doi.org/10.1111/j.1756-1051.2012.01211.x
Dawes, M.A., Hagedorn, F., Zumbrunn, T., Handa, I.T., Hattenschwiler, S., Wipf, S. and Rixen, C. (2011) Growth and Community Responses of Alpine Dwarf Shrubs to in Situ CO2 Enrichment and Soil Warming. New Phytologist, 191, 806-818. http://dx.doi.org/10.1111/j.1469-8137.2011.03722.x
Walker, M.D., Wahren, C.H., Hollister, R.D., Henry, G.H.R., Ahlquist, L.E., Alatalo, J.M., Bret-Harte, M.S., Calef, M.P., Callaghan, T.V., Carroll, A.B., et al. (2006) Plant Community Responses to Experimental Warming across the Tundra Biome. Proceedings of the National Academy of Sciences of the United States of America, 103, 1342-1346. http://dx.doi.org/10.1073/pnas.0503198103
Butler, S.M., Melillo, J.M., Johnson, J.E., Mohan, J., Steudler, P.A., Lux, H., Burrows, E., Smith, R.M., Vario, C.L., Scott, L., Hill, T.D., Aponte, N. and Bowles, F. (2012) Soil Warming Alters Nitrogen Cycling in a New England Forest: Implications for Ecosystem Function and Structure. Oecologia, 168, 819-828. http://dx.doi.org/10.1007/s00442-011-2133-7
Melillo, J.M., Butler, S., Johnson, J., Mohan, J., Steudler, P., Lux, H., Burrows, E., Bowles, F., Smith, R., Scott, L., Vario, C., Hill, T., Burton, A., Zhou, Y.M. and Tang, J. (2011) Soil Warming, Carbon-Nitrogen Interactions, and Forest Carbon Budgets. Proceedings of the National Academy of Sciences of the United States of America, 108, 9508-9512. http://dx.doi.org/10.1073/pnas.1018189108
Zhang, S., Dang, Q.L. and Yu, X. (2006) Nutrient and [CO2] Elevation Had Synergistic Effects on Biomass Production but Not on Biomass Allocation of White Birch Seedlings. Forest Ecology and Management, 234, 238-244. http://dx.doi.org/10.1016/j.foreco.2006.07.017
Cao, B., Dang, Q.L., Yu, X. and Zhang, S. (2008) Effects of [CO2] and Nitrogen on Morphological and Biomass Traits of White Birch (Betula papyrifera) Seedlings. Forest Ecology and Management, 254, 217-224. http://dx.doi.org/10.1016/j.foreco.2007.08.002