ALBERT

Notes: Root dynamics are important for plant, ecosystem and global carbon cycling. Changes in root dynamics caused by rising atmospheric CO2 not only have the potential to moderate further CO2 increases, but will likely affect forest function. We used FACE (Free-Air CO2 Enrichment) to expose three 30-m diameter plots in a 13-year-old loblolly pine (Pinus taeda) forest to elevated (ambient + 200 µL L−1) atmospheric CO2. Three identical fully instrumented plots were implemented as controls (ambient air only). We quantified root dynamics from October 1998 to October 1999 using minirhizotrons. In spite of 16% greater root lengths and 24% more roots per minirhizotron tube, the effects of elevated atmospheric CO2 on root lengths and numbers were not statistically significant. Similarly, production and mortality were also unaffected by the CO2 treatment, even though annual root production and mortality were 26% and 46% greater in elevated compared to ambient CO2 plots. Average diameters of live roots present at the shallowest soil depth were, however, significantly enhanced in CO2-enriched plots. Mortality decreased with increasing soil depth and the slopes of linear regression lines (mortality vs. depth) differed between elevated and ambient CO2 treatments, reflecting the significant CO2 by depth interaction. Relative root turnover (root flux/live root pool) was unchanged by exposure to elevated atmospheric CO2. Results from this study suggest modest, if any, increases in ecosystem-level root productivity in CO2-enriched environments.

Notes: Increasing atmospheric CO2 concentration has led to concerns about potential effects on production agriculture as well as agriculture's role in sequestering C. In the fall of 1997, a study was initiated to compare the response of two crop management systems (conventional and conservation) to elevated CO2. The study used a split-plot design replicated three times with two management systems as main plots and two CO2 levels (ambient=375 μL L−1 and elevated CO2=683 μL L−1) as split-plots using open-top chambers on a Decatur silt loam (clayey, kaolinitic, thermic Rhodic Paleudults). The conventional system was a grain sorghum (Sorghum bicolor (L.) Moench.) and soybean (Glycine max (L.) Merr.) rotation with winter fallow and spring tillage practices. In the conservation system, sorghum and soybean were rotated and three cover crops were used (crimson clover (Trifolium incarnatum L.), sunn hemp (Crotalaria juncea L.), and wheat (Triticum aestivum L.)) under no-tillage practices. The effect of management on soil C and biomass responses over two cropping cycles (4 years) were evaluated. In the conservation system, cover crop residue (clover, sunn hemp, and wheat) was increased by elevated CO2, but CO2 effects on weed residue were variable in the conventional system. Elevated CO2 had a greater effect on increasing soybean residue as compared with sorghum, and grain yield increases were greater for soybean followed by wheat and sorghum. Differences in sorghum and soybean residue production within the different management systems were small and variable. Cumulative residue inputs were increased by elevated CO2 and conservation management. Greater inputs resulted in a substantial increase in soil C concentration at the 0–5 cm depth increment in the conservation system under CO2-enriched conditions. Smaller shifts in soil C were noted at greater depths (5–10 and 15–30 cm) because of management or CO2 level. Results suggest that with conservation management in an elevated CO2 environment, greater residue amounts could increase soil C storage as well as increase ground cover.

Notes: A critical global climate change issue is how increasing concentrations of atmospheric CO2 and ground-level O3 will affect agricultural productivity. This includes effects on decomposition of residues left in the field and availability of mineral nutrients to subsequent crops. To address questions about decomposition processes, a 2-year experiment was conducted to determine the chemistry and decomposition rate of aboveground residues of soybean (Glycine max (L.) Merr.) grown under reciprocal combinations of low and high concentrations of CO2 and O3 in open-top field chambers. The CO2 treatments were ambient (370 μmol mol−1) and elevated (714 μmol mol−1) levels (daytime 12 h averages). Ozone treatments were charcoal-filtered air (21 nmol mol−1) and nonfiltered air plus 1.5 times ambient O3 (74 nmol mol−1) 12 h day−1. Elevated CO2 increased aboveground postharvest residue production by 28–56% while elevated O3 suppressed it by 15–46%. In combination, inhibitory effects of added O3 on biomass production were largely negated by elevated CO2. Plant residue chemistry was generally unaffected by elevated CO2, except for an increase in leaf residue lignin concentration. Leaf residues from the elevated O3 treatments had lower concentrations of nonstructural carbohydrates, but higher N, fiber, and lignin levels. Chemical composition of petiole, stem, and pod husk residues was only marginally affected by the elevated gas treatments. Treatment effects on plant biomass production, however, influenced the content of chemical constituents on an areal basis. Elevated CO2 increased the mass per square meter of nonstructural carbohydrates, phenolics, N, cellulose, and lignin by 24–46%. Elevated O3 decreased the mass per square meter of these constituents by 30–48%, while elevated CO2 largely ameliorated the added O3 effect. Carbon mineralization rates of component residues from the elevated gas treatments were not significantly different from the control. However, N immobilization increased in soils containing petiole and stem residues from the elevated CO2, O3, and combined gas treatments. Mass loss of decomposing leaf residue from the added O3 and combined gas treatments was 48% less than the control treatment after 20 weeks, while differences in decomposition of petiole, stem, and husk residues among treatments were minor. Decreased decomposition of leaf residues was correlated with lower starch and higher lignin levels. However, leaf residues only comprised about 20% of the total residue biomass assayed so treatment effects on mass loss of total aboveground residues were relatively small. The primary influence of elevated atmospheric CO2 and O3 concentrations on decomposition processes is apt to arise from effects on residue mass input, which is increased by elevated CO2 and suppressed by O3.

Notes: Consequences of increasing atmospheric CO2 concentration on plant structure, an important determinant of physiological and competitive success, have not received sufficient attention in the literature. Understanding how increasing carbon input will influence plant developmental processes, and resultant form, will help bridge the gap between physiological response and ecosystem level phenomena. Growth in elevated CO2 alters plant structure through its effects on both primary and secondary meristems of shoots and roots. Although not well established, a review of the literature suggests that cell division, cell expansion, and cell patterning may be affected, driven mainly by increased substrate (sucrose) availability and perhaps also by differential expression of genes involved in cell cycling (e.g. cyclins) or cell expansion (e.g. xyloglucan endotransglycosylase). Few studies, however, have attempted to elucidate the mechanistic basis for increased growth at the cellular level. Regardless of specific mechanisms involved, plant leaf size and anatomy are often altered by growth in elevated CO2, but the magnitude of these changes, which often decreases as leaves mature, hinges upon plant genetic plasticity, nutrient availability, temperature, and phenology. Increased leaf growth results more often from increased cell expansion rather than increased division. Leaves of crop species exhibit greater increases in leaf thickness than do leaves of wild species. Increased mesophyll and vascular tissue cross-sectional areas, important determinates of photosynthetic rates and assimilate transport capacity, are often reported. Few studies, however, have quantified characteristics more reflective of leaf function such as spatial relationships among chlorenchyma cells (size, orientation, and surface area), intercellular spaces, and conductive tissue. Greater leaf size and/or more leaves per plant are often noted; plants grown in elevated CO2 exhibited increased leaf area per plant in 66% of studies, compared to 28% of observations reporting no change, and 6% reported a decrease in whole plant leaf area. This resulted in an average net increase in leaf area per plant of 24%. Crop species showed the greatest average increase in whole plant leaf area (+ 37%) compared to tree species (+ 14%) and wild, nonwoody species (+ 15%). Conversely, tree species and wild, nontrees showed the greatest reduction in specific leaf area (– 14% and – 20%) compared to crop plants (– 6%). Alterations in developmental processes at the shoot apex and within the vascular cambium contributed to increased plant height, altered branching characteristics, and increased stem diameters. The ratio of internode length to node number often increased, but the length and sometimes the number of branches per node was greater, suggesting reduced apical dominance. Data concerning effects of elevated CO2 on stem/branch anatomy, vital for understanding potential shifts in functional relationships of leaves with stems, roots with stems, and leaves with roots, are too few tomake generalizations. Growth in elevated CO2 typically leads to increased root length, diameter, and altered branching patterns. Altered branching characteristics in both shoots and roots may impact competitive relationships above and below the ground. Understanding how increased carbon assimilation affects growth processes (cell division, cell expansion, and cell patterning) will facilitate a better understanding of how plant form will change as atmospheric CO2 increases. Knowing how basic growth processes respond to increased carbon inputs may also provide a mechanistic basis for the differential phenotypic plasticity exhibited by different plant species/functional types to elevated CO2.

Notes: Abstract Models describing plant and ecosystem N cycles require an accurate assessment of root physiological uptake capacity for NH 4 + and NO 3 - under field conditions. Traditionally, rates of ion uptake in field-grown plants are determined by using excised root segments incubated for a short period in an assay solution containing N either as a radioactive or stable isotope tracer (e.g., 36ClO3 as a NH 4 + analogue, 14CH3NH3 as an NO 3 - analogue or 15NH 4 + and 15NO 3 - ). Although reliable, this method has several drawbacks. For example, in addition to radioactive safety issues, purchase and analysis of radioactive and stable isotopes is relatively expensive and can be a major limitation. More importantly, because excision effectively interrupts exchange of compounds between root and shoot (e.g., carbohydrate supply to root and N transport to shoot), the assay must be conducted quickly to avoid such complications. Here we present a novel field method for simultaneous measurements of NH 4 + and NO 3 - uptake kinetics in intact root systems. The application of this method is demonstrated using two tree species; red maple (Acer rubrum) and sugar maple (Acer saccharum) and two crop species soybean (Glycine max) and sorghum (Sorghum bicolor). Plants were grown in open-top chambers at either ambient or elevated levels of atmospheric CO2 at two separate US national sites involved in CO2 research. Absolute values of net uptake rates and the kinetic parameters determined by our method were found to be in agreement with the literature reports. Roots of the crop species exhibited a greater uptake capacity for both N forms relative to tree species. Elevated CO2 did not significantly affect kinetics of N uptake in species tested except in red maple where it increased root uptake capacity, V, for NH 4 + . The application, reliability, advantages and disadvantages of the method are discussed in detail.

Notes: Abstract Crops of tomorrow are likely to grow under higher levels of atmospheric CO2. Fundamental crop growth processes will be affected and chief among these is carbon allocation. The root to shoot ratio (R:S, defined as dry weight of root biomass divided by dry weight of shoot biomass) depends upon the partitioning of photosynthate which may be influenced by environmental stimuli. Exposure of plant canopies to high CO2 concentration often stimulates the growth of both shoot and root, but the question remains whether elevated atmospheric CO2 concentration will affect roots and shoots of crop plants proportionally. Since elevated CO2 can induce changes in plant structure and function, there may be differences in allocation between root and shoot, at least under some conditions. The effect of elevated atmospheric CO2 on carbon allocation has yet to be fully elucidated, especially in the context of changing resource availability. Herein we review root to shoot allocation as affected by increased concentrations of atmospheric CO2 and provide recommendations for further research. Review of the available literature shows substantial variation in R:S response for crop plants. In many cases (59.5%) R:S increased, in a very few (3.0%) remained unchanged, and in others (37.5%) decreased. The explanation for these differences probably resides in crop type, resource supply, and other experimental factors. Efforts to understand allocation under CO2 enrichment will add substantially to the global change response data base.

Notes: Abstract One-year old, nursery-grown longleaf pine (Pinus palustris Mill.) seedlings were grown in 45-L pots containing a coarse sandy medium and were exposed to two concentrations of atmospheric CO2 (365 or 720 μmol-1) and two levels of nitrogen (N) fertility (40 or 400 kg N ha-1 yr-1) within open top chambers for 20 months. At harvest, needles, stems, coarse roots, and fine roots were separated and weighed. Subsamples of each tissue were frozen in liquid N, lyophilized at -50°C, and ground to pass a 0.2 mm sieve. Tissue samples were analyzed for carbon (C), N, nonpolar extractives (fats, waxes, and oils = FWO), nonstructural carbohydrates (total sugars and starch), and structural carbohydrates (cellulose, lignin, and tannins). Increased dry weights of each tissue were observed under elevated CO2 and with high N; however, main effects of CO2 were significant only on belowground tissues. The high N fertility tended to result in increased partitioning of biomass aboveground, resulting in significantly lower root to shoot ratios. Elevated CO2 did not affect biomass allocation among tissues. Both atmospheric CO2 and N fertility tended to affect concentration of C compounds in belowground, more than aboveground, tissues. Elevated CO2 resulted in lower concentrations of starch, cellulose, and lignin, but increased concentrations of FWO in root tissues. High N fertility increased the concentration of starch, cellulose, and tannins, but resulted in lower concentrations of lignin and FWO in roots. Differences between CO2 concentrations tended to occur only with high N fertility. Atmospheric CO2 did not affect allocation patterns for any compound; however the high N treatment tended to result in a lower percentage of sugars, cellulose, and lignin belowground.