Competition increasingly dominates the responsiveness of juvenile beech and spruce to elevated CO₂ and/or O₃ concentrations throughout two subsequent growing seasons
Saplings of Fagus sylvatica and Picea abies were grown in mono‐ and mixed cultures in a 2‐year phytotron study under all four combinations of ambient and elevated ozone (O3) and carbon dioxide (CO2) concentrations. The hypotheses tested were (1) that the competitiveness of beech rather than spruce i...
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Published in | Global change biology Vol. 11; no. 9; pp. 1387 - 1401 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Oxford, UK
Blackwell Science Ltd
01.09.2005
Blackwell Publishing Ltd |
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Abstract | Saplings of Fagus sylvatica and Picea abies were grown in mono‐ and mixed cultures in a 2‐year phytotron study under all four combinations of ambient and elevated ozone (O3) and carbon dioxide (CO2) concentrations. The hypotheses tested were (1) that the competitiveness of beech rather than spruce is negatively affected by the exposure to enhanced O3 concentrations, (2) spruce benefits from the increase of resource availability (elevated CO2) in the mixed culture and (3) that the responsiveness of plants to CO2 and O3 depends on the type of competition (i.e. intra vs. interspecific).
Beech displayed a competitive disadvantage when growing in mixture with spruce: after two growing seasons under interspecific competition, beech showed significant reductions in leaf gas exchange, biomass development and crown volume as compared with beech plants growing in monoculture. In competition with spruce, beech appeared to be nitrogen (N)‐limited, whereas spruce tended to benefit in terms of its plant N status.
The responsiveness of the juvenile trees to the atmospheric treatments differed between species and was dominated by the type of competition: spruce growth benefited from elevated CO2 concentrations, while beech growth suffered from the enhanced O3 regime. In general, interspecific competition enhanced these atmospheric treatment effects, supporting our hypotheses. Significant differences in root : shoot biomass ratio between the type of competition under both elevated O3 and CO2 were not caused by readjustments of biomass partitioning, but were dependent on tree size.
Our study stresses that competition is an important factor driving plant development, and suggests that the knowledge about responses of plants to elevated CO2 and/or O3, acquired from plants growing in monoculture, may not be transferred to plants grown under interspecific competition as typically found in the field. |
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AbstractList | Saplings of Fagus sylvatica and Picea abies were grown in mono‐ and mixed cultures in a 2‐year phytotron study under all four combinations of ambient and elevated ozone (O3) and carbon dioxide (CO2) concentrations. The hypotheses tested were (1) that the competitiveness of beech rather than spruce is negatively affected by the exposure to enhanced O3 concentrations, (2) spruce benefits from the increase of resource availability (elevated CO2) in the mixed culture and (3) that the responsiveness of plants to CO2 and O3 depends on the type of competition (i.e. intra vs. interspecific).
Beech displayed a competitive disadvantage when growing in mixture with spruce: after two growing seasons under interspecific competition, beech showed significant reductions in leaf gas exchange, biomass development and crown volume as compared with beech plants growing in monoculture. In competition with spruce, beech appeared to be nitrogen (N)‐limited, whereas spruce tended to benefit in terms of its plant N status.
The responsiveness of the juvenile trees to the atmospheric treatments differed between species and was dominated by the type of competition: spruce growth benefited from elevated CO2 concentrations, while beech growth suffered from the enhanced O3 regime. In general, interspecific competition enhanced these atmospheric treatment effects, supporting our hypotheses. Significant differences in root : shoot biomass ratio between the type of competition under both elevated O3 and CO2 were not caused by readjustments of biomass partitioning, but were dependent on tree size.
Our study stresses that competition is an important factor driving plant development, and suggests that the knowledge about responses of plants to elevated CO2 and/or O3, acquired from plants growing in monoculture, may not be transferred to plants grown under interspecific competition as typically found in the field. Saplings of Fagus sylvatica and Picea abies were grown in mono- and mixed cultures in a 2-year phytotron study under all four combinations of ambient and elevated ozone (O3) and carbon dioxide (CO2) concentrations. The hypotheses tested were (1) that the competitiveness of beech rather than spruce is negatively affected by the exposure to enhanced O3 concentrations, (2) spruce benefits from the increase of resource availability (elevated CO2) in the mixed culture and (3) that the responsiveness of plants to CO2 and O3 depends on the type of competition (i.e. intra vs. interspecific). Beech displayed a competitive disadvantage when growing in mixture with spruce: after two growing seasons under interspecific competition, beech showed significant reductions in leaf gas exchange, biomass development and crown volume as compared with beech plants growing in monoculture. In competition with spruce, beech appeared to be nitrogen (N)-limited, whereas spruce tended to benefit in terms of its plant N status. The responsiveness of the juvenile trees to the atmospheric treatments differed between species and was dominated by the type of competition: spruce growth benefited from elevated CO2 concentrations, while beech growth suffered from the enhanced O3 regime. In general, interspecific competition enhanced these atmospheric treatment effects, supporting our hypotheses. Significant differences in root : shoot biomass ratio between the type of competition under both elevated O3 and CO2 were not caused by readjustments of biomass partitioning, but were dependent on tree size. Our study stresses that competition is an important factor driving plant development, and suggests that the knowledge about responses of plants to elevated CO2 and/or O3, acquired from plants growing in monoculture, may not be transferred to plants grown under interspecific competition as typically found in the field. [PUBLICATION ABSTRACT] |
Author | Göttlein, Axel Grams, Thorsten E. E. Matyssek, Rainer Blaschke, Helmut Kozovits, Alessandra R. |
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References_xml | – reference: Lippert M, Steiner K, Payer H-D et al. (1996) Assessing the impact of ozone on photosynthesis of European beech (Fagus sylvatica L.) in environmental chambers. Trees, 10, 268-275. – reference: Dickson RE, Coleman MD, Pechter P et al. (2001) Growth and crown architecture of two aspen genotypes exposed to interacting ozone and carbon dioxide. Environmental Pollution, 115, 319-334. – reference: Bloom AJ, Chapin FS, Mooney HA (1985) Resource limitation in plants - an economic analogy. Annual Review of Ecology and Systems, 16, 363-392. – reference: Matyssek R, Keller T, Koike T (1993) Branch growth and leaf gas-exchange of Populus tremula exposed to low ozone concentrations throughout two growing seasons. Environmental Pollution, 79, 1-7. – reference: Wang Z, Göttlein A, Bartonek G (2001) Effects of growing roots of Norway spruce (Picea abies Karst.) and European beech (Fagus sylvatica) on rhizosphere soil solution chemistry. Journal of Plant Nutrition and Soil Science, 164, 35-41. – reference: Küppers M (1985) Carbon relations and competition between woody species in a central European hedgerow. IV. Growth form and partitioning. Oecologia, 66, 343-352. – reference: Volin JC, Reich PB, Givnish TJ (1998) Elevated carbon dioxide ameliorates the effects of ozone on photosynthesis and growth: species respond similarly regardless of photosynthetic pathway or plant functional group. New Phytologist, 138, 315-325. – reference: Poorter H, Navas M-L (2003) Plant growth and competition at elevated CO2: on winners, losers and functional groups. New Phytologist, 157, 175-198. – reference: Aerts R (1999) Interspecific competition in natural plant communities: mechanism, trade-offs and plant-soil feedbacks. Journal of Experimental Botany, 50, 29-37. – reference: Lemaire G, Millard P (1999) An ecophysiological approach to modelling resource fluxes in competing plants. Journal of Experimental Botany, 50, 15-28. – reference: Thiel S, Döhring T, Köfferlein M et al. (1996) A phytotron for plant stress research: how far can artificial lighting compare to natural sunlight? Journal of Plant Physiology, 148, 456-463. – reference: Pretzsch H (2002) A unified law of spatial allometry for woody and herbaceous plants. Plant Biology, 4, 159-166. – reference: Bortier K, Ceulemans R, De Temmerman L (2000) Effects of ozone exposure on growth and photosynthesis of beech seedlings (Fagus sylvatica). New Phytologist, 146, 271-280. – reference: Schulze ED, Hall AE, Lange OL et al. (1982) A portable steady-state porometer for measuring the carbon-dioxide and water-vapor exchanges of leaves under natural conditions. Oecologia, 53, 141-145. – reference: Yokozawa M, Kubota Y, Hara T (1996) Crown architecture and species coexistence in plant communities. Annals of Botany, 78, 437-447. – reference: Oren R, Ellsworth DS, Johnsen et al. (2001) Soil fertility limits carbon sequestration by forest ecosystems in a CO2-enriched atmosphere. Nature, 411, 469-472. – reference: Barnes JD, Pfirrmann T, Steiner K et al. (1995) Effects of elevated CO2, elevated O3 and potassium deficiency on Norway spruce (Picea abies (L.) Karst.): seasonal changes in photosynthesis and non-structural carbohydrate content. Plant, Cell and Environment, 18, 1345-1357. – reference: Vanderheyden D, Skelly J, Innes J et al. (2001) Ozone exposure thresholds and foliar injury on forest plants in Switzerland. Environmental Pollution, 111, 321-331. – reference: Umeki K (1995) Importance of crown position and morphological plasticity in competitive interaction in a population of Xanthium canadense. Annals of Botany, 75, 259-265. – reference: Maurer S, Egli P, Spinnler D et al. (1999) Carbon and water fluxes in Beech-Spruce model ecosystems in response to long-term exposure to atmospheric CO2 enrichment and increased nitrogen deposition. 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Snippet | Saplings of Fagus sylvatica and Picea abies were grown in mono‐ and mixed cultures in a 2‐year phytotron study under all four combinations of ambient and... Saplings of Fagus sylvatica and Picea abies were grown in mono- and mixed cultures in a 2-year phytotron study under all four combinations of ambient and... |
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SubjectTerms | air pollution allometry Biomass Botany Carbon dioxide Competition elevated atmospheric gases European beech (Fagus sylvatica) Fagus sylvatica Gas exchange Growing season growth chambers interspecific competition juvenility Monoculture nitrogen content Norway spruce (Picea abies) Ozone partitioning Picea abies plant competition plant nutrition Resource availability tree growth Trees whole-plant nitrogen status |
Title | Competition increasingly dominates the responsiveness of juvenile beech and spruce to elevated CO₂ and/or O₃ concentrations throughout two subsequent growing seasons |
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