Climate and species affect fine root production with long-term fertilization in acidic tussock tundra near Toolik Lake,Alaska

Long-term fertilization of acidic tussock tundra has led to changes in plant species composition, increases in aboveground production and biomass and substantial losses of soil organic carbon (SOC). Root litter is an important input to SOC pools, although little is known about fine root demography in tussock tundra. In this study, we examined the response of fine root production and live standing fine root biomass to short- and long-term fertilization, as changes in fine root demography may contribute to observed declines in SOC. Live standing fine root biomass increased with long-term fertilization, while fine root production declined, reflecting replacement of the annual fine root system of Eriophorum vaginatum, with the long-lived fine roots of Betula nana. Fine root production increased in fertilized plots during an unusually warm growing season, but remained unchanged in control plots, consistent with observations that B. nana shows a positive response to climate warming. Calculations based on a few simple assumptions suggest changes in fine root demography with long-term fertilization and species replacement could account for between 20 and 39% of the observed declines in SOC stocks.     

Response of tussock tundra to elevated carbon dioxide regimes: analysis of ecosystem CO2 flux through nonlinear modeling

Summary The response of tussock tundra to elevated atmospheric concentrations of CO₂ was measured at Toolik Lake, Alaska in the summer of 1983. Computer-controlled greenhouses were used to determine diurnal ecosystem flux of CO₂ under four treatments: 340 ppm, 510 ppm, and 680 ppm CO₂, as well as 680 ppm CO₂ with a four degree centrigrade increase in temperature. For the seven days of data analyzed, net daily CO₂ flux was significantly different between treatments. Net uptake was positively correlated with CO₂ concentration in the chamber and negatively correlated with temperature. A nonlinear model was used to analyze this data set and to determine some of the reasons for different net CO₂ flux. This model allowed an estimation of light utilization efficiency, total conductance of CO₂, and a comparable measure of total respiration. From this analysis we conclude that nutrient limitations in the arctic decrease the capacity of tundra plants to make use of elevated CO₂ concentrations. The plants respond by decreasing conductance in the presence of elevated CO₂, which results in approximately equal gross uptake rates for the three CO₂ treatments. Apparent changes in system respiration result in higher net uptake under elevated CO₂ but this may be due to biases in the data. The treatment with increased temperature exhibited higher conductances and, consequently, higher gross uptake of CO₂ than the other treatments. Higher temperatures, however, also increase respiration with the result being lower net uptake than would be expected in the absence of temperature inscreases.     

Soil respiration of Alaskan tundra at elevated atmospheric carbon dioxide concentrations

Summary CO₂ efflux from tussock tundra in Alaska that had been exposed to elevated CO₂ for 2.5 growing seasons was measured to assess the effect of long- and short-term CO₂ enrichment on soil respiration. Long-term treatments were: 348, 514, and 683 μll⁻¹ CO₂ and 680 μll⁻¹ CO₂+4°C above ambient. Measurements were made at 5 CO₂ concentrations between 87 and 680 μll⁻¹ CO₂. Neither long- or short-term CO₂ enrichment significantly affected soil CO₂ efflux. Tundra developed at elevated temperature and 680 μll⁻¹ CO₂ had slightly higher, but not statistically different, mean respiration rates compared to untreated tundra and to tundra under CO₂ control alone.     

Carbon dioxide and methane exchange of a north-east Siberian tussock tundra

Carbon dioxide, energy flux measurements and methane chamber measurements were carried out in an arctic wet tussock grassland located on a flood plane of the Kolyma river in NE Siberia over a summer period of 155 days in 2002 and early 2003. Respiration was also measured in April 2004. The study region is characterized by late thaw of the top soil (mid of June) and periodic spring floods. A stagnant water table below the grass canopy is fed by thawing of the active layer of permafrost and by flood water. The climate is continental with average daily temperature in the warmest months of 13°C (maximum temperature at midday: 28°C by the end of July), dry air (maximum vapour pressure deficit at midday: 28 hPa) and low rainfall of 50 mm during summer (July–September). Summer evaporation (July–September: 103 mm) exceeded rainfall by a factor of 2. The daily average Bowen ratio (H/LE) was 0.62 during the growing season. Net ecosystem CO₂ uptake reached 10 μmol m⁻² s⁻¹ and was related to photon flux density (PFD) and vapour pressure deficit (VPD). The cumulative annual net carbon flux from the atmosphere to the terrestrial surface was estimated to be about −38 g C m⁻² yr⁻¹ (negative flux depicts net carbon sink). Winter respiration was extrapolated using the Lloyd and Taylor function. The net carbon balance is composed of a high rate of assimilation in a short summer and a fairly large but uncertain respiration mainly during autumn and spring. Methane flux (about 12 g C m⁻² measured over 60 days) was 25% of C uptake during the same period of time (end of July to end of September). Assuming that CH₄ was emitted only in summer, and taking the greenhouse gas warming potential of CH₄ vs. CO₂ into account (factor 23), the study site was a greenhouse gas source (at least 200 g C_equivalent m⁻² yr⁻¹). Comparing different studies in wetlands and tundra ecosystems as related to latitude, we expect that global warming would rather increase than decrease the CO₂-C sink.     

Winter regulation of tundra litter carbon and nitrogen dynamics

Mass and nitrogen (N) dynamics of leaf litter measured in Alaskan tussock tundra differed greatly from measurements of these processes made in temperate ecosystems. Nearly all litter mass and N loss occurred during the winter when soils were mostly frozen. Litter lost mass during the first summer, but during the subsequent two summers when biological activity was presumably higher than it is during winter, litter mass remained constant and litter immobilized N. By contrast, litter lost significant mass and N over both winters of measurement. Mass loss and N dynamics were unaffected by microsite variation in soil temperature and moisture. Whether wintertime mass and N loss resulted from biological activity during winter or from physical processes (e.g., fragmentation or leaching) associated with freeze-thaw is unknown, but has implications for how future climate warming will alter carbon (C) and N cycling in tundra. We hypothesize that spring runoff over permafrost as soils melt results in significant losses of C and N from litter, consistent with the observed influx of terrestrial organic matter to tundra lakes and streams after snow melt and the strong N limitation of terrestrial primary production.     

Ammonium and nitrate as nitrogen sources in two Eriophorum species

Summary We compared ammonium and nitrate nutrition in Eriophorum scheuchzeri and E. vaginatum, two Alaskan sedges that are native to high- and low-fertility sites, respectively. When grown in solution culture, the two species were similar in their kinetics of NH _inf4 ^sup+ NO _inf3 ^sup- absorption: at nitrogen concentrations below 50 M, net NH _inf4 ^sup+ and NO _inf3 ^sup- were absorbed at similar rates, but at higher concentrations, net uptake of NO _inf3 ^sup- was significantly faster than that of NH _inf4 ^sup+ . The two species also showed similar abilities to assimilate NO _inf3 ^sup- . Growth of E. vaginatum under NO _inf3 ^sup- nutrition was only slightly less than that under NH _inf4 ^sup+ . The observed similarities between these species from contrasting edaphic habitats indicate that factors other than tissue-specific rates of nitrogen acquisition and assimilation may underlie local adaptation to soil N fertility. Moreover, the capacity of these species to exploit NO _inf3 ^sup- as a N source supports the view that NO _inf3 ^sup- availability may be significant even in wet, acidic, arctic soils.     

Effects of increased soil water availability on grassland ecosystem carbon dioxide fluxes

There is considerable interest in how ecosystems will respond to changes in precipitation. Alterations in rain and snowfall are expected to influence the spatio-temporal patterns of plant and soil processes that are controlled by soil moisture, and potentially, the amount of carbon (C) exchanged between the atmosphere and ecosystems. Because grasslands cover over one third of the terrestrial landscape, understanding controls on grassland C processes will be important to forecast how changes in precipitation regimes will influence the global C cycle. In this study we examined how irrigation affects carbon dioxide (CO₂) fluxes in five widely variable grasslands of Yellowstone National Park during a year of approximately average growing season precipitation. We irrigated plots every 2 weeks with 25% of the monthly 30-year average of precipitation resulting in plots receiving approximately 150% of the usual growing season water in the form of rain and supplemented irrigation. Ecosystem CO₂ fluxes were measured with a closed chamber-system once a month from May-September on irrigated and unirrigated plots in each grassland. Soil moisture was closely associated with CO₂ fluxes and shoot biomass, and was between 1.6% and 11.5% higher at the irrigated plots (values from wettest to driest grassland) during times of measurements. When examining the effect of irrigation throughout the growing season (May–September) across sites, we found that water additions increased ecosystem CO₂ fluxes at the two driest and the wettest sites, suggesting that these sites were water-limited during the climatically average precipitation conditions of the 2005 growing season. In contrast, no consistent responses to irrigation were detected at the two sites with intermediate soil moisture. Thus, the ecosystem CO₂ fluxes at those sites were not water-limited, when considering their responses to supplemental water throughout the whole season. In contrast, when we explored how the effect of irrigation varied temporally, we found that irrigation increased ecosystem CO₂ fluxes at all the sites late in the growing season (September). The spatial differences in the response of ecosystem CO₂ fluxes to irrigation likely can be explained by site specific differences in soil and vegetation properties. The temporal effects likely were due to delayed plant senescence that promoted plant and soil activity later into the year. Our results suggest that in Yellowstone National Park, above-normal amounts of soil moisture will only stimulate CO₂ fluxes across a portion of the ecosystem. Thus, depending on the topographic location, grassland CO₂ fluxes can be water-limited or not. Such information is important to accurately predict how changes in precipitation/soil moisture will affect CO₂ dynamics and how they may feed back to the global C cycle.     

Influence of free air CO2 enrichment (EUROFACE) and nitrogen fertilisation on the anatomy of juvenile wood of three poplar species after coppicing

Populus × euramericana, P. alba, and P. nigra clones were exposed to ambient or elevated (about 550 ppm) CO₂ concentrations under field conditions (FACE) in central Italy. After three growing seasons, the plantation was coppiced. FACE was continued and in addition, one-half of each experimental plot was fertilised with nitrogen. Growth and anatomical wood properties were analysed in secondary sprouts. In the three poplar clones, most of the growth and anatomical traits showed no uniform response pattern to elevated [CO₂] or N-fertilisation. In cross-sections of young poplar stems, tension wood amounted to 2–10% of the total area and was not affected by elevated CO₂. In P. nigra, N-fertilisation caused an about twofold increase in tension wood, but not in the other clones. The formation of tension wood was not related to diameter or height growth of the shoots. In P. × euramericana N-fertilisation resulted in significant reductions in fibre lengths. In all three genotypes, N-fertilisation caused significant decreases in cell wall thickness. In P. × euramericana and P. alba elevated [CO₂] also caused decreases in wall thickness, but less pronounced than nitrogen. In P. nigra and P. × euramericana elevated [CO₂] induced increases in vessel diameters. These results show that elevated [CO₂] and N-fertilisation affect wood structural development in a clone specific manner. However, the combination of these environmental factors resulted in overall losses in cell wall area of 5–12% in all three clones suggesting that in future climate scenarios negative effects on wood quality are to be anticipated if increases in atmospheric CO₂ concentration were accompanied by increased N availability.     

Compensatory responses of CO2 exchange and biomass allocation and their effects on the relative growth rate of ponderosa pine in different CO2 and temperature regimes

Increases in the concentration of atmospheric carbon dioxide may have a fertilizing effect on plant growth by increasing photosynthetic rates and therefore may offset potential growth decreases caused by the stress associated with higher temperatures and lower precipitation. However, plant growth is determined both by rates of net photosynthesis and by proportional allocation of fixed carbon to autotrophic tissue and heterotrophic tissue. Although CO₂ fertilization may enhance growth by increasing leaf-level assimilation rates, reallocation of biomass from leaves to stems and roots in response to higher concentrations of CO₂ and higher temperatures may reduce whole-plant assimilation and offset photosynthetic gains. We measured growth parameters, photosynthesis, respiration, and biomass allocation of Pinus ponderosa seedlings grown for 2 months in 2×2 factorial treatments of 350 or 650 bar CO₂ and 10/25° C or 15/30° C night/day temperatures. After 1 month in treatment conditions, total seedling biomass was higher in elevated CO₂, and temperature significantly enhanced the positive CO₂ effect. However, after 2 months the effect of CO₂ on total biomass decreased and relative growth rates did not differ among CO₂ and temperature treatments over the 2-month growth period even though photosynthetic rates increased 7% in high CO₂ treatments and decreased 10% in high temperature treatments. Additionally, CO₂ enhancement decreased root respiration and high temperatures increased shoot respiration. Based on CO₂ exchange rates, CO₂ fertilization should have increased relative growth rates (RGR) and high temperatures should have decreased RGR. Higher photosynthetic rates caused by CO₂ fertilization appear to have been mitigated during the second month of exposure to treatment conditions by a 3% decrease in allocation of biomass to leaves and a 9% increase in root:shoot ratio. It was not clear why diminished photosynthetic rates and increased respiration rates at high temperatures did not result in lower RGR. Significant diametrical and potentially compensatory responses of CO₂ exchange and biomass allocation and the lack of differences in RGR of ponderosa pine after 2 months of exposure of high CO₂ indicate that the effects of CO₂ fertilization and temperature on whole-plant growth are determined by complex shifts in biomass allocation and gas exchange that may, for some species, maintain constant growth rates as climate and atmospheric CO₂ concentrations change. These complex responses must be considered together to predict plant growth reactions to global atmospheric change, and the potential of forest ecosystems to sequester larger amounts of carbon in the future.     

Effects of nitrogen supply and elevated carbon dioxide on construction cost in leaves of Pinus taeda (L.) seedlings

Seedlings of loblolly pine (Pinus taeda L.) were grown under varying conditions of soil nitrogen and atmospheric carbon dioxide availability to investigate the interactive effects of these resources on the energetic requirements for leaf growth. Increasing the ambient CO₂ partial pressure from 35 to 65 Pa increased seedling growth only when soil nitrogen was high. Biomass increased by 55% and photosynthesis increased by 13% after 100 days of CO₂ enrichment. Leaves from seedlings grown in high soil nitrogen were 7.0% more expensive on a g glucose g^–1 dry mass basis to produce than those grown in low nitrogen, while elevated CO₂ decreased leaf cost by 3.5%. Nitrogen and CO₂ availability had an interactive effect on leaf construction cost expressed on an area basis, reflecting source-sink interactions. When both resources were abundant, leaf construction cost on an area basis was relatively high (81.8±3.0 g glucose m^–2) compared to leaves from high nitrogen, low CO₂ seedlings (56.3±3.0 g glucose m^–2) and low nitrogen, low CO₂ seedlings (67.1±2.7 g glucose m^–2). Leaf construction cost appears to respond to alterations in the utilization of photoassimilates mediated by resource availability.     

Limitations on Sphagnum growth and net primary production in the foothills of the Philip Smith Mountains,Alaska

Summary In the foothills of the Philip Smith Mountains, Brooks Range, Alaska, tussock tundra occurs on rolling hills and in valleys that were shaped by Pleistocene glaciations. During the 1986 and 1987 summer seasons, Sphagnum growth and production were determined in water tracks on tundra slopes that acted to channel water flow to the valley bottom stream and in intertrack tundra areas that were relatively homogeneous with respect to downslope drainage. Measurements were made under ambient environmental conditions and on mosses receiving supplemental irrigation in each area. Growth rate for Sphagnum spp. (cm shoot length increase/day) was low and relatively constant in intertrack tundra and highest but quite variable in water tracks. A strong negative correlation was found between Sphagnum spp. growth rate and solar irradiance in the shady environment below Salix canopies in the water tracks. Estimates of net annual dry weight (DW) production for Sphagnum spp. ranged from 0.10 g DW dm^-2 yr^-1 in intertrack tundra vegetation to 1.64 g DW dm^-2 yr^-1 in well-shaded water tracks. Experimental water additions had little effect on growth and production in intertrack tundra and well-developed water tracks, but significantly increased growth in a weakly-developed water track community. Low production over large areas of tundra slopes may occur due to presence of slow growing species resistant to dessication in intertrack tundra as opposed to rapidly growing less compact species within the limited extent of water tracks. We hypothesize that species capable of rapid growth occur also in weakly-developed water tracks, and that these are water-limited more often than plants occurring in well-developed water track situations. Where experienced, high light intensity may additionally limit growth due to photoinhibition.     

Long- and short-term effects of reindeer grazing on tundra wetland vegetation

We studied long-term (50 years) and short-term (4 years) effects of summer grazing of reindeer on subarctic tundra wetland vegetation. The long-term effects of summer grazing were studied by comparing vegetation on Finnish and Norwegian sides of the fence line separating reindeer grazing regimes. The Finnish side was intensively grazed and trampled throughout the year, whereas the Norwegian side was grazed in winter. Experimental fences were erected to examine short-term effects of grazing exclusion. Both in the long- and short-term, summer grazing decreased the height of Salix lapponum whereas the short-term effects on willow cover were less clear than the long-term effects. In contrast, Carex spp. benefited from grazing. Long-term grazing had little effect on total bryophyte cover. Grazing had negligible effects on the nutrient content of leaves of S. lapponum and Eriophorum angustifolium. We conclude that tundra wetlands can withstand moderately high grazing pressure sustained over several decades.     

Irradiance and temperature effects on photosynthesis of tussock tundra Sphagnum mosses from the foothills of the Philip Smith Mountains,Alaska

Summary Photosynthetic characteristics of three species of Sphagnum common in the foothills of the Brooks Range on the North Slope of Alaska were investigated. Generally, light-saturated rates of net photosynthesis decreased in the order S. squarrosum, S. angustifolium, and S. warnstorfii when plants were grown under common growth chamber conditions. For field-grown S. angustifolium, average light compensation point at 10°C was 37 mol m^-2s^-1 photosynthetic photon flux density (PPFD), and light saturation occurred between 250 and 500 mol m^-2 s^-1. At 20°C, compensation point increased to 127 mol m^-2s^-1 and the PPFD required for light saturation increased to approximately 500 mol m^-2s^-1, while maximum rates of CO₂ uptake increased only slightly. Light response curves of chamber-grown plants exhibited substantially lower compensation points and higher light-saturated rates of CO₂ assimilation than field-grown material, due perhaps to a higher percentage of green, photosynthetically competent tissue. All three species exhibited broad responses to temperature, with optima near 20°C, and maintained at least 75% of maximum assimilation between approx. 13° and 30°C. Rates at 5°C were approx. 50% of maximum. Studies of the microclimate of Sphagnum at the field research site suggest that CO₂ uptake should occur at near light-saturated rates during the day in open tussock tundra but that PPFD may often be limiting under Salix and Betula canopies in a water track drainage. Simulations using a simple model provided a seasonal estimate of 0.78 g dry weight (DW) of S. angustifolium produced from each initial g of photosynthetic tissue under willow canopies, assuming no water limitations. Although the simulation model suggests that production would be 66% higher in open tussock tundra, S. angustifolium is rarely found in this potentially more stressful habitat. To explain the relative abundance of Sphagnum in shaded water track areas as compared to open tussock tundra, we postulate that the vascular plant canopies provide protection from adverse effects of high temperatures, excess irradiance and reduced water availability. Under conditions of normal water availability, removal of the vascular plant cover did not affect the tissue water content of S. squarrosum, but resulted in a strong decrease in photosynthetic capacity, accompanied by chlorophyll bleaching. These results suggest that photoinhibition may limit production under certain conditions.     

The global-scale temperature and moisture dependencies of soil organic carbon decomposition: an analysis using a mechanistic decomposition model

Since the decomposition rate of soil organic carbon (SOC) varies as a function of environmental conditions, global climate change is expected to alter SOC decomposition dynamics, and the resulting changes in the amount of CO₂ emitted from soils will feedback onto the rate at which climate change occurs. While this soil feedback is expected to be significant because the amount of SOC is substantially more than the amount of carbon in the atmosphere, the environmental dependencies of decomposition at global scales that determine the magnitude of the soil feedback have remained poorly characterized. In this study, we address this issue by fitting a mechanistic decomposition model to a global dataset of SOC, optimizing the model’s temperature and moisture dependencies to best match the observed global distribution of SOC. The results of the analysis indicate that the temperature sensitivity of decomposition at global scales (Q ₁₀=1.37) is significantly less than is assumed by many terrestrial ecosystem models that directly apply temperature sensitivity from small-scale studies, and that the maximal rate of decomposition occurs at higher moisture values than is assumed by many models. These findings imply that the magnitude of the soil decomposition feedback onto rate of global climate change will be less sensitive to increases in temperature, and modeling of temperature and moisture dependencies of SOC decomposition in global-scale models should consider effects of scale.     

Effect of elevated atmospheric carbon dioxide on the use of foliar application of Bacillus thuringiensis

Toxins from Bacillus thuringiensis have beenused as pest management tools for more than 50 years. The effect of these toxins depends on the quantityof Bacillus thuringiensis (Bt) toxins ingestedby susceptible insects. Food ingestion is affected byCO₂ concentration; plants grown in elevatedCO₂ often have increased carbon/nitrogen ratios(C/N), resulting in greater leaf area consumption. Therefore, we hypothesized that elevated CO₂would improve the efficacy of foliar applications ofB. thuringiensis. Cotton plants were grown ateither ambient (360–380 l/l) or elevated CO₂(900 l/l). Groups of plants in both CO₂treatments were exposed to low (30 mg/kg soil/week) orhigh (130 mg/kg soil/week) nitrogen (N) fertilizationlevels in a split plot design. The resulting plantswere assessed for N and carbon (C) contents. Leafdisks from the same plants were dipped in a Btsolution and then fed to Spodoptera exigua(Hübner), an insect species of considerableeconomic importance. Elevated CO₂ significantlyreduced total N, and increased the C/N. Nitrogenfertilization significantly affected consumption byearly stadia larvae, larval weight gain, and relativegrowth rate (RGR). Interactions between CO₂concentration and N fertilization level significantlyimpacted late stadia larval food consumption, andthrough differential Bt toxin intake, affectedduration of larval stage and mortality to the adultstage. We conclude that the elevated atmosphericCO₂ concentrations expected in the next centurywill interact with commercial fertilization practicesto enhance the efficacy of B. thuringiensisformulations applied topically to crops. Theimplications for improved control are discussed.     

Carbon balance of a tropical savanna of northern Australia

Through estimations of above- and below-ground standing biomass, annual biomass increment, fine root production and turnover, litterfall, canopy respiration and total soil CO₂ efflux, a carbon balance on seasonal and yearly time-scales is developed for a Eucalypt open-forest savanna in northern Australia. This carbon balance is compared to estimates of carbon fluxes derived from eddy covariance measurements conducted at the same site. The total carbon (C) stock of the savanna was 204±53 ton C ha^–1, with approximately 84% below-ground and 16% above-ground. Soil organic carbon content (0–1 m) was 151±33 ton C ha^–1, accounting for about 74% of the total carbon content in the ecosystem. Vegetation biomass was 53±20 ton C ha^–1, 39% of which was found in the root component and 61% in above-ground components (trees, shrubs, grasses). Annual gross primary production was 20.8 ton C ha^–1, of which 27% occurred in above-ground components and 73% below-ground components. Net primary production was 11 ton C ha^–1 year^–1, of which 8.0 ton C ha^–1 (73%) was contributed by below-ground net primary production and 3.0 ton C ha^–1 (27%) by above-ground net primary production. Annual soil carbon efflux was 14.3 ton C ha^–1 year^–1. Approximately three-quarters of the carbon flux (above-ground, below-ground and total ecosystem) occur during the 5–6 months of the wet season. This savanna site is a carbon sink during the wet season, but becomes a weak source during the dry season. Annual net ecosystem production was 3.8 ton C ha^–1 year^–1.     

Atmospheric carbon dioxide and fertilizer nitrogen effects on radiation interception by rice 1

In order to predict the potential impacts of global change, it is important to understand the impact of increasing global atmospheric [CO₂] on the growth and yield of crop plants. The objectives of this study were to determine the interaction of N fertilization rates and atmospheric [CO₂] on radiation interception and radiation-use efficiency of rice (Oryza sativa L. cv. IR72) grown under tropical field conditions. Rice plants were grown inside open top chambers in a lowland rice field at the International Rice Research Institute in the Philippines at ambient (about 350 μmol mol^-1) or elevated (about 600 μmol mol^-1 during the 1993 wet season and 700 μmol mol^-1 during the 1994 dry season) in combination with three levels of applied N (0, 50 or 100 kg N ha^-1 in the wet season; 0, 90 or 200 kg N ha-1 in the dry season). Light interception was not directly affected by [CO₂], but elevated [CO₂] indirectly increased light interception through increasing total absorbed N. Plant N requirement for radiation interception was similar for rice grown under ambient [CO₂] or elevated [CO₂] treatments. The conversion efficiency of intercepted radiation to dry matter, radiation-use efficiency (RUE), was about 35% greater at elevated [CO₂] than at ambient [CO₂]. The relationship between leaf N and RUE was curvilinear. At ambient [CO₂], RUE was fairly stable across levels of leaf N, but leaf N less than about 2.5% resulted in lower RUE for plants grown with elevated [CO₂] than for plant grown at ambient [CO₂]. Decreased leaf N with increased [CO₂], therefore decreased RUE of rice plants grown at elevated [CO₂]. When predicting responses of rice to elevated [CO₂], RUE should be adjusted with a decrease in leaf N. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effects of elevated CO2 and temperature on secondary compounds in the needles of Scots pine (Pinus sylvestris L.)

The aim of this study was to evaluate the long-term effects of elevated CO₂ concentration (doubling of ambient CO₂ concentration) and temperature (2–6°C elevation) on the concentration and content of secondary compounds in the needles of Scots pine (Pinus sylvestris L.) saplings grown in closed-top environmental chambers. The chamber treatments included (1) ambient temperature and CO₂, (2) ambient temperature and elevated CO₂, (3) elevated temperature and ambient CO₂, and (4) elevated temperature and elevated CO₂. The needle sampling and analyses of monoterpenes, HPLC-phenolics and condensed tannins in current- and 1-year-old needles were made in two consecutive years. The results showed that the effects of elevation of CO₂ and temperature were greatest on the monoterpene concentration in the needles while the concentration of HPLC-phenolics remained almost unaffected by the changed growing conditions. Most of the observed decrease in monoterpene concentration was caused by the CO₂ enrichment while the effect of elevated temperature alone was not as significant. The accumulation of condensed tannins tended to increase due to the elevation of CO₂ alone compensating the reduced carbon allocation to monoterpenes. Overall, the responses of the concentrations of secondary compounds to the elevation of CO₂ and temperature are variable and depend strongly on the properties and characteristics of each compound as well as on the interrelation between the production of these compounds and the primary production of trees.