The effects of elevated atmospheric CO 2 concentration on growth of forest tree species are difficult to predict because practical limitations restrict experiments to much shorter than the average life-span of a tree. Long-term, processbased computer models must be used to extrapolate from shorter-term experiments. A key problem is to ensure a strong flow of information between experiments and models. In this study, meta-analysis techniques were used to summarize a suite of photosynthetic model parameters obtained from 15 field-based elevated [CO 2 ] experiments on European forest tree species. The parameters studied are commonly used in modelling photosynthesis, and include observed light-saturated photosynthetic rates (A max ), the potential electron transport rate (J max ), the maximum Rubisco activity (V cmax ) and leaf nitrogen concentration on mass (N m ) and area (N a ) bases. Across all experiments, light-saturated photosynthesis was strongly stimulated by growth in elevated [CO 2 ]. However, significant down-regulation of photosynthesis was also observed; when measured at the same CO 2 concentration, photosynthesis was reduced by 10-20%. Wullschleger (1993) and Ryan et al. (1994), are therefore invaluable for improving model predictions.These challenges were faced by the ECOCRAFT network, a group of laboratories conducting field-based experiments on the effects of elevated [CO 2 ] on European forest tree species. The network has existed since 1991, and the experimental results up to 1995 have been compiled by Jarvis (1998). Besford, Mousseau & Matteucci (1998) reviewed observations of photosynthetic rates in the ECOCRAFT experiments, and concluded that 'both up and down-regulation of photosynthesis has been found. Downregulation appears to be associated with either poor nutrient status or accumulation of starch, occurs more often late in the growing season and in the older needles of conifers.'The group then faced the problem of quantifying these results in such a way that they could be included in models. This problem was addressed by establishing a central relational database of model parameters (Medlyn & Jarvis 1999). The parameters required, and the methods of deriving them from experimental data, were agreed upon by project working groups comprising both experimentalists and modellers. This paper reports on the photosynthesis parameters from the database, presenting them in formats useful for modelling. First, lists of photosynthesis parameters for different species, extracted from the database, are presented. This catalogue should provide a useful resource for modellers. Second, quantitative methods (i.e. meta-analysis) are used to estimate the effects of elevated [CO 2 ] on the parameters across experiments. Different hypotheses for the effects of long-term elevated [CO 2 ] on photosynthesis are examined. This analysis aids our understanding of photosynthetic responses to elevated [CO 2 ] and suggests ways in which we can improve model formulation.Photosynthesis is a key process when stu...

), at elevated temperature (ambient + 2·8-6·2 ∞ ∞ ∞ ∞ C depending on the time of the year) and in a combination of elevated CO 2 and temperature in closed-top chambers. The treatments were started in August 1996. At elevated temperature, the needles that were grown in the first year (i.e. the 1997 cohort) were thinner, had thinner mesophyll in the abaxial side, thinner vascular cylinder and lower stomatal density than those grown at ambient temperature. The proportion of mesophyll area occupied by vascular cylinder or intercellular spaces were not changed. Lower stomatal density apparently did not lead to decreased use of water, as these needles had higher concentrations of less mobile nutrients (Ca, Mg, B, Zn and Mn), which could indicate increased total transpiration. In the 1997 and 1998 cohorts, elevation of temperature decreased concentrations of N, P, K, S and Cu. In the 1999 cohort, contradictory, higher concentrations of N and S at elevated temperature may be related to increased nutrient mineralization in the soil. Elevation of CO 2 did not affect stomatal density, needle thickness, thickness of epidermis or hypodermis, vascular cylinder or intercellular spaces. Concentrations of N, P, S and Cu decreased at elevated CO 2 . Reductions were transient and most distinct in the 1997 cohort. The effects of CO 2 and temperature were in some cases interactive, which meant that in the combined treatment stomatal density decreased less than at elevated temperature, and concentrations of nutrients decreased less than expected on the basis of separate treatments, whereas the thickness of the epidermis and hypodermis decreased more than in the separate treatments. In conclusion, alterations in the anatomy and stomatal density of Scots pine needles were more distinct at elevated temperature than at elevated CO 2 . Both elevated CO 2 and temperature-induced changes in nutrient concentrations that partly corresponded to the biochemical and photosynthetic alterations in the same cohorts (

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Naturally regenerated 20-25-year-old Scots pine (Pinus sylvestris L.) trees were grown in open-top chambers in the presence of an elevated temperature or CO(2) concentration, or both. The elevated temperature treatment was administered year-round for 3 years. The CO(2) treatment was applied between April 15 and September 15 for 2 years. The photosynthetic responses of 1- and 2-year-old needles to varying photon flux densities (0-1500 micro mol m(-2) s(-1)) and CO(2) concentrations (350, 700 and 1400 micro mol mol(-1)) during measurement were determined. The CO(2) treatment alone increased maximum photosynthetic rate and light-use efficiency, but decreased dark respiration rate, light compensation and light saturation regardless of needle age. In contrast, the temperature treatment decreased maximum photosynthetic rate and photosynthetic efficiency, but increased dark respiration rate, light compensation and light saturation. The aging of needles affected the photosynthetic performance of the shoots; values of all parameters except photosynthetic efficiency were less in 2- than in 1-year-old needles. The CO(2) treatment decreased and the temperature treatment enhanced the reduction in maximum photosynthesis due to needle aging.

Impacts of elevated temperature and carbon dioxide concentration ([CO2]) on wood properties of 15-year-old Scots pines (Pinus sylvestris L.) grown under conditions of low nitrogen supply were investigated in open-top chambers. The treatments consisted of (i) ambient temperature and ambient [CO2] (AT+AC), (ii) ambient temperature and elevated [CO2] (AT+EC), (iii) elevated temperature and ambient [CO2] (ET+AC) and (iv) elevated temperature and elevated [CO2] (ET+EC). Wood properties analyzed for the years 1992-1994 included ring width, early- and latewood width and their proportions, intra-ring wood density (minimum, maximum and mean, as well as early- and latewood densities), mean fiber length and chemical composition of the wood (cellulose, hemicellulose, lignin and acetone extractive concentration). Absolute radial growth over the 3-year period was 54% greater in AT+EC trees and 30 and 25% greater in ET+AC and ET+EC trees, respectively, than in AT+AC trees. Neither elevated temperature nor elevated [CO2] had a statistically significant effect on ring width, early- and latewood widths or their proportions. Both latewood density and maximum intra-ring density were increased by elevated [CO2], whereas fiber length was increased by elevated temperature. Hemicellulose concentration decreased and lignin concentration increased significantly in response to elevated temperature. There were no statistically significant interaction effects of elevated temperature and elevated [CO2] on the wood properties, except on earlywood density.