Plant Nitrogen Dynamics in Shortgrass Steppe under Elevated Atmospheric Carbon Dioxide

The direct and indirect effects of increasing levels of atmospheric carbon dioxide (CO₂) on plant nitrogen (N) content were studied in a shortgrass steppe ecosystem in northeastern Colorado, USA. Beginning in 1997 nine experimental plots were established: three open-top chambers with ambient CO₂ levels (approximately 365 mol mol^–1), three open-top chambers with twice-ambient CO₂ levels (approximately 720 mol mol^–1), and three unchambered control plots. After 3 years of growing-season CO₂ treatment, the aboveground N concentration of plants grown under elevated atmospheric CO₂ decreased, and the carbon–nitrogen (C:N) ratio increased. At the same time, increased aboveground biomass production under elevated atmospheric CO₂ conditions increased the net transfer of N out of the soil of elevated-CO₂ plots. Aboveground biomass production after simulated herbivory was also greater under elevated CO₂ compared to ambient CO₂. Surprisingly, no significant changes in belowground plant tissue N content were detected in response to elevated CO₂. Measurements of individual species at peak standing phytomass showed significant effects of CO₂ treatment on aboveground plant tissue N concentration and significant differences between species in N concentration, suggesting that changes in species composition under elevated CO₂ will contribute to overall changes in nutrient cycling. Changes in plant N content, driven by changes in aboveground plant N concentration, could have important consequences for biogeochemical cycling rates and the long-term productivity of the shortgrass steppe as atmospheric CO₂ concentrations increase.     

Elevated CO2 enhances water relations and productivity and affects gas exchange in C3 and C4 grasses of the Colorado shortgrass steppe.

Six open‐top chambers were installed on the shortgrass steppe in north‐eastern Colorado, USA from late March until mid‐October in 1997 and 1998 to evaluate how this grassland will be affected by rising atmospheric CO₂. Three chambers were maintained at current CO₂ concentration (ambient treatment), three at twice ambient CO₂, or approximately 720 μmol mol^?1 (elevated treatment), and three nonchambered plots served as controls. Above‐ground phytomass was measured in summer and autumn during each growing season, soil water was monitored weekly, and leaf photosynthesis, conductance and water potential were measured periodically on important C₃ and C₄ grasses. Mid‐season and seasonal above‐ground productivity were enhanced from 26 to 47% at elevated CO₂, with no differences in the relative responses of C₃/C₄ grasses or forbs. Annual above‐ground phytomass accrual was greater on plots which were defoliated once in mid‐summer compared to plots which were not defoliated during the growing season, but there was no interactive effect of defoliation and CO₂ on growth. Leaf photosynthesis was often greater in Pascopyrum smithii (C₃) and Bouteloua gracilis (C₄) plants in the elevated chambers, due in large part to higher soil water contents and leaf water potentials. Persistent downward photosynthetic acclimation in P. smithii leaves prevented large photosynthetic enhancement for elevated CO₂‐grown plants. Shoot N concentrations tended to be lower in grasses under elevated CO₂, but only Stipa comata (C₃) plants exhibited significant reductions in N under elevated compared to ambient CO₂ chambers. Despite chamber warming of 2.6 °C and apparent drier chamber conditions compared to unchambered controls, above‐ground production in all chambers was always greater than in unchambered plots. Collectively, these results suggest increased productivity of the shortgrass steppe in future warmer, CO₂ enriched environments.     

Tree species diversity interacts with elevated CO2 to induce a greater root system response

As a consequence of land‐use change and the burning of fossil fuels, atmospheric concentrations of CO₂ are increasing and altering the dynamics of the carbon cycle in forest ecosystems. In a number of studies using single tree species, fine root biomass has been shown to be strongly increased by elevated CO₂. However, natural forests are often intimate mixtures of a number of co‐occurring species. To investigate the interaction between tree mixture and elevated CO₂, Alnus glutinosa, Betula pendula and Fagus sylvatica were planted in areas of single species and a three species polyculture in a free‐air CO₂ enrichment study (BangorFACE). The trees were exposed to ambient or elevated CO₂ (580 μmol mol^?1) for 4 years. Fine and coarse root biomass, together with fine root turnover and fine root morphological characteristics were measured. Fine root biomass and morphology responded differentially to the elevated CO₂ at different soil depths in the three species when grown in monocultures. In polyculture, a greater response to elevated CO₂ was observed in coarse roots to a depth of 20 cm, and fine root area index to a depth of 30 cm. Total fine root biomass was positively affected by elevated CO₂ at the end of the experiment, but not by species diversity. Our data suggest that existing biogeochemical cycling models parameterized with data from species grown in monoculture may be underestimating the belowground response to global change.     

Root dynamics in a semi-natural grassland in relation to atmospheric carbon dioxide enrichment,soil water and shoot biomass

Plant responses to increasing atmospheric CO₂ concentrations have been studied intensively. However, the effects of elevated CO₂ on root dynamics, which is important for global carbon budgets as well as for nutrient cycling in ecosystems, has received much less attention. We used minirhizotrons inside open-top chambers to study the effects of elevated atmospheric carbon dioxide concentration on root dynamics in a nutrient-poor semi-natural grassland in central Sweden. We conducted our investigation over three consecutive growing seasons during which three treatments were applied at the site: Elevated (≈ 700 μmol mol^-1) and ambient (≈ 360 μmol mol^-1) chamber levels of CO₂ and a control, without a chamber. During 1997, a summer with two dry periods, the elevated treatment compared with ambient had 25% greater mean root counts, 65% greater above-ground biomass and 15% greater soil moisture. The chambers seemed responsible for changes in root dynamics, whereas the elevated CO₂ treatment in general increased the absolute sum of root counts compared with the ambient chamber. In 1998, a wet growing season, there were no significant differences in shoot biomass or root dynamics and both chamber treatments had lower soil moisture than the control. We found that as seasonal dryness increased, the ratio of elevated – ambient shoot biomass production increased while the root to shoot ratio decreased. We conclude that this grasslands response to elevated CO₂ is dependent on seasonal weather conditions and that CO₂ enrichment will most significantly increase production in such a grassland when under water stress. This revised version was published online in June 2006 with corrections to the Cover Date.     

Root biomass and nutrient dynamics in a scrub-oak ecosystem under the influence of elevated atmospheric CO2

Elevated CO₂ can increase fine root biomass but responses of fine roots to exposure to increased CO₂ over many years are infrequently reported. We investigated the effect of elevated CO₂ on root biomass and N and P pools of a scrub-oak ecosystem on Merritt Island in Florida, USA, after 7 years of CO₂ treatment. Roots were removed from 1-m deep soil cores in 10-cm increments, sorted into different categories (<0.25 mm, 0.25–1 mm, 1–2 mm, 2 mm to 1 cm, >1 cm, dead roots, and organic matter), weighed, and analyzed for N, P and C concentrations. With the exception of surface roots <0.25 mm diameter, there was no effect of elevated CO₂ on root biomass. There was little effect on C, N, or P concentration or content with the exception of dead roots, and <0.25 mm and 1–2 mm diameter live roots at the surface. Thus, fine root mass and element content appear to be relatively insensitive to elevated CO₂. In the top 10 cm of soil, biomass of roots with a diameter of <0.25 mm was depressed by elevated CO₂. Elevated CO₂ tended to decrease the mass and N content of dead roots compared to ambient CO₂. A decreased N concentration of roots <0.25 mm and 1–2 mm in diameter under elevated CO₂ may indicate reduced N supply in the elevated CO₂ treatment. Our study indicated that elevated CO₂ does not increase fine root biomass or the pool of C in fine roots. In fact, elevated CO₂ tends to reduce biomass and C content of the most responsive root fraction (<0.25 mm roots), a finding that may have more general implications for understanding C input into the soil at higher atmospheric CO₂ concentrations.     

Enhanced root system C-sink activity,water relations and aspects of nutrient acquisition in mycotrophic Bouteloua gracilis subjected to CO2 enrichment

In order to better elucidate fixed-C partitioning, nutrient acquisition and water relations of prairie grasses under elevated [CO₂], we grew the C₄ grass Bouteloua gracilis (H.B.K.) lag ex Steud. from seed in soil-packed, column-lysimeters in two growth chambers maintained at current ambient [CO₂] (350 μL L⁻¹) and twice enriched [CO₂] (700 μL L⁻¹). Once established, plants were deficit irrigated; growth chamber conditions were maintained at day/night temperatures of 25/16°C, relative humidities of 35%/90% and a 14-hour photoperiod to simulate summer conditions on the shortgrass steppe in eastern Colorado. After 11 weeks of growth, plants grown under CO₂ enrichment had produced 35% and 65% greater total and root biomass, respectively, and had twice the level of vesicular-arbuscular mycorrhizal (VAM) infection (19.8% versus 10.8%) as plants grown under current ambient [CO₂]. The CO₂-enriched plants also exhibited greater leaf water potentials and higher plant water use efficiencies. Plant N uptake was reduced by CO₂ enrichment, while P uptake appeared little influenced by CO₂ regime. Under the conditions of the experiment, CO₂ enrichment increased root biomass and VAM infection via stimulated growth and adjustments in C partitioning below-ground. The U.S. Government right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The U.S. Government right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged.     

Plant biodiversity on shortgrass steppe after 55 years of zero,light, moderate,or heavy cattle grazing

Shortgrass steppe rangeland near Nunn, Colorado, USA, has been lightly,moderately, or heavily grazed by cattle, or protected from grazing inexclosures, for 55 years. Plant species biodiversity and evenness were greatestin lightly- and moderately-grazed pastures. Both pastures weredominated by the warm-season shortgrass Boutelouagracilis, but the cool-season midgrasses Pascopyrumsmithii and Stipa comata contributedsignificantly to biomass production on the lightly-grazed pasture, asthey did in the exclosures. Diversity was least in the exclosures, which werestrongly dominated by the cactus Opuntia polyacantha.Buchloë dactyloides, another warm-seasonshortgrass, and Bouteloua gracilis were co-dominantsunder heavy grazing, and diversity was intermediate. Plant community structureand diversity were controlled by selective grazing by cattle and soildisturbance by cattle and rodents. Shortgrass steppe moderately or heavilygrazed by cattle was similar to and probably as sustainable as steppe grazed formillenia by bison and other wild ungulates.     

Root response to CO2 enrichment and nitrogen supply in loblolly pine

This paper examines how elevated CO₂ and nitrogen (N) supply affect plant characteristics of loblolly pine (Pinus taeda L.) with an emphasis on root morphology. Seedlings were grown in greenhouses from seeds during one growing season at two atmospheric CO₂ concentrations (375 and 710 μL L^-1) and two N levels (High and Low). Root morphological characteristics were determined using a scanner and an image analysis program on a Macintosh computer. In the high N treatment, elevated CO₂ increased total plant dry weight by 80% and did not modify root to shoot (R/S) dry weight ratio, and leaf and plant N concentration at the end of the growing season. In the low N treatment, elevated CO₂ increased total dry weight by 60%. Plant and leaf N concentration declined and R/S ratio tended to increase. Nitrogen uptake rate on both a root length and a root dry weight basis was greater at elevated CO₂ in the high N treatment and lower in the low N treatment. We argue that N stress resulting from short exposures to nutrients might help explain the lower N concentrations observed at high CO₂ in other experiments; Nitrogen and CO₂ levels modified root morphology. High N increased the number of secondary lateral roots per length of first order lateral root and high CO₂ increased the length of secondary lateral roots per length of first order lateral root. Number and length of first order lateral roots were not modified by either treatment. Specific root length of main axis, and to a lower degree, of first order laterals, declined at high CO₂, especially at high N. Basal stem diameter and first order root diameters increased at high CO₂, especially at high N. Elevated CO₂ increased the proportion of upper lateral roots within the root system.     

Relationship Between Root Biomass and Soil Organic Matter Pools in the Shortgrass Steppe of Eastern Colorado

We examined the distribution of soil organic carbon (SOC) fractions and roots with depth to improve our understanding of belowground carbon dynamics in the shortgrass steppe of northern Colorado. Weaver and others (1935) found that the surface 15 cm of soil contained over 70% of the total roots found in a tallgrass prairie soil profile, while only accounting for 40% of the profile soil organic matter. We asked whether the relationship between roots and SOC that Weaver and others (1935) found in the tallgrass prairie was also found in the shortgrass steppe. Weaver and others (1935) suggested that the dissimilarity between belowground biomass and SOC with depth is the result of variability in decomposition rates. In an effort to determine whether patterns of SOC are the result of short-term plant input patterns or decomposition, we measured the ¹⁴C content of potentially mineralizable C and particulate organic matter (POM) C ten years after pulse labeling shortgrass steppe vegetation. We also estimated the mass specific decomposition rate constant (kPOM) for POM C through a shortgrass steppe soil profile. We found that the distribution of roots and SOM in the shortgrass steppe were similar to those observed in tallgrass prairie (Weaver and others 1935), with a higher proportion of total root biomass in the surface soils than total soil organic matter. Fifty-seven percent of root biomass was found in the surface 15-cm, while this same soil layer contained 23 percent of profile soil organic C. We measured the highest accumulation of ¹⁴C at the soil surface (12.0 ng ¹⁴C·m^-2·cm^-1 depth), with the least accumulation from 75-100 cm (0.724 ng ¹⁴C·m^-2·cm^-1 depth). The highest values of potentially mineralizable C were at the soil surface, with no significant differences in total mineralizable C among the 10-100 cm soil depths. The contribution of POM C to total C reached a profile minimum at the 15-20 cm depth increment, with profile maxima in the surface 5 cm and from 75-100 cm. We estimated that the proportion of particulate organic matter lost annually (kPOM) reached a profile maximum of 0.097 yr^-1 within the 10-15 cm depth increment. The 75-100 cm depth increment had the lowest kPOM value at 0.058 yr^-1. Thus, within the same physical fraction of SOC, decomposition rates vary with depth by nearly twofold. This pattern of high decomposition rates from 10-15 cm with lower decomposition rates at the soil surface and deeper in the soil profile may be the result of higher water availability in sub-surface soils in the shortgrass steppe.     

Root to shoot ratio of crops as influenced by CO2

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.Abbreviations R:S root to shoot ratio, dry weight basis     

Root production and mortality under elevated atmospheric carbon dioxide

An essential component of an understanding of carbon flux is the quantification of movement through the root carbon pool. Although estimates have been made using radiocarbon, the use of minirhizotrons provides a direct measurement of rates of root birth and death. We have measured root demographic parameters under a semi-natural grassland and for wheat. The grassland was studied along a natural altitudinal gradient in northern England, and similar turf from the site was grown in elevated CO₂ in solardomes. Root biomass was enhanced under elevated CO₂. Root birth and death rates were both increased to a similar extent in elevated CO₂, so that the throughput of carbon was greater than in ambient CO₂, but root half-lives were shorter under elevated CO₂ only under a Juncus/Nardus sward on a peaty gley soil, and not under a Festuca turf on a brown earth soil. In a separate experiment, wheat also responded to elevated CO₂ by increased root production, and there was a marked shift towards surface rooting: root development at a depth of 80–85 cm was both reduced and delayed. In conjunction with published results for trees, these data suggest that the impact of elevated CO₂ will be system-dependent, affecting the spatio-temporal pattern of root growth in some ecosystems and the rate of turnover in others. Turrnover is also sensitive to temperature, soil fertility and other environmental variables, all of which are likely to change in tandem with atmospheric CO₂ concentrations. Differences in turnover and time and location of rhizodeposition may have a large effect on rates of carbon cycling.     

Elevated Atmospheric CO2 Alters Soil Microbial Communities Associated with Trembling Aspen (Populus tremuloides) Roots

Global atmospheric CO₂ levels are expected to double within the next 50 years. To assess the effects of increased atmospheric CO₂ on soil ecosystems, cloned trembling aspen (Populus tremuloides) seedlings were grown individually in 1 m³ open bottom root boxes under either elevated (720 ppm, ELEV) or ambient CO₂ (360 ppm, AMB). After 5 years, soil cores (40 cm depth) were collected from the root boxes and divided into 0–20 cm and 20–40 cm fractions. ELEV treatment resulted in significant decreases in both soil nitrate and total soil nitrogen in both the 0–20 cm and 20–40 cm soil fractions, with a 47% decrease in soil nitrate and a 50% decrease in total soil nitrogen occurring in the 0–20 cm fraction. ELEV treatment did not result in a significant change in the amount of soil microbial biomass. However, analysis of indicator phospholipid fatty acids (PLFA) indicated that ELEV treatment did result in significant increases in PLFA indicators for fungi and Gram-negative bacteria in the 0–20 cm fraction. Terminal restriction fragment length polymorphism (T-RFLP) analysis was used to analyze the composition of the soil bacterial communities (using primers targeting the 16SrRNA gene) and the soil fungal communities (using primers targeting the intergenic transcribed spacer region). T-RFLP analysis revealed shifts in both bacterial and fungal community structure, as well as increases in both bacterial and fungal species richness with ELEV treatment. These results indicated that increased atmospheric CO₂ had significant effects on both soil nutrient availability and the community composition of soil microbes associated with aspen roots.     

Carbon dynamics and microbial activity in tallgrass prairie exposed to elevated CO2 for 8 years

Alterations in microbial mineralization and nutrient cycling may control the long-term response of ecosystems to elevated CO₂. Because micro-organisms constitute a labile fraction of potentially available N and are regulators of decomposition, an understanding of microbial activity and microbial biomass is crucial. Tallgrass prairie was exposed to twice ambient CO₂ for 8 years beginning in 1989. Starting in 1991 and ending in 1996, soil samples from 0 to 5 and 5 to 15 cm depths were taken for measurement of microbial biomass C and N, total C and N, microbial activity, inorganic N and soil water content. Because of increased water-use-efficiency by plants, soil water content was consistently and significantly greater in elevated CO₂ compared to ambient treatments. Soil microbial biomass C and N tended to be greater under elevated CO₂ than ambient CO₂ in the 5–15 cm depth during most years, and in the month of October, when analyzed over the entire study period. Microbial activity was significantly greater at both depths in elevated CO₂ than ambient conditions for most years. During dry periods, the greater water content of the surface 5 cm soil in the elevated CO₂ treatments increased microbial activity relative to the ambient CO₂ conditions. The increase in microbial activity under elevated CO₂ in the 5–15 cm layer was not correlated with differences in soil water contents, but may have been related to increases in soil C inputs from enhanced root growth and possibly greater root exudation. Total soil C and N in the surface 15 cm were, after 8 years, significantly greater under elevated CO₂ than ambient CO₂. Our results suggest that decomposition is enhanced under elevated CO₂ compared with ambient CO₂, but that inputs of C are greater than the decomposition rates. Soil C sequestration in tallgrass prairie and other drought-prone grassland systems is, therefore, considered plausible as atmospheric CO₂ increases. This revised version was published online in June 2006 with corrections to the Cover Date.     

Root dynamics and demography in shortgrass steppe under elevated CO2, and comments on minirhizotron methodology

The dynamics and demography of roots were followed for 5 years that spanned wet and drought periods in native, semiarid shortgrass steppe grassland exposed to ambient and elevated atmospheric CO₂ treatments. Elevated compared with ambient CO₂ concentrations resulted in greater root‐length growth (+52%), root‐length losses (+37%), and total pool sizes (+41%). The greater standing pool of roots under elevated compared with ambient CO₂ was because of the greater number of roots (+35%), not because individuals were longer. Loss rates increased relatively less than growth rates because life spans were longer (+41%). The diameter of roots was larger under elevated compared with ambient CO₂ only in the upper soil profile. Elevated CO₂ affected root architecture through increased branching. Growth‐to‐loss ratio regressions to time of equilibrium indicate very long turnover times of 5.8, 7.0, and 5.3 years for control, ambient, and elevated CO₂, respectively. Production was greater under elevated compared with ambient CO₂ both below‐ and aboveground, and the above‐ to belowground ratios did not differ between treatments. However, estimates of belowground production differed among methods of calculation using minirhizotron data, as well as between minirhizotron and root‐ingrowth methods. Users of minirhizotrons may need to consider equilibration in terms of both new growth and disappearance, rather than just growth. Large temporal pulses of root initiation and termination rates of entire individuals were observed (analogous to birth–death rates), and precipitation explained more of the variance in root initiation than termination. There was a dampening of the pulsing in root initiation and termination under elevated CO₂ during both wet and dry periods, which may be because of conservation of soil water reducing the suddenness of wet pulses and duration and severity of dry pulses. However, a very low degree of synchrony was observed between growth and disappearance (production and decomposition).     

The influence of plant species,fertilization and elevated CO2 on soil aggregate stability

We tested the effects of plant species, fertilization and elevated CO₂ on water-stable soil aggregation. Five annual grassland species and a plant community were grown in outdoor mesocosms for 4 years, with and without NPK fertilization, at ambient or elevated atmospheric CO₂ concentrations. Aggregate stability (resistance of aggregates to slaking) in the top 0.15 m of soil differed among plant species. However, the more diverse plant community did not enhance aggregate stability relative to most monocultures. Species differences in aggregate stability were positively correlated with soil active bacterial biomass, but did not correlate with root biomass or fungal length. Plant species did not affect aggregate stability lower in the soil profile (0.15–0.45 m), where soil biological activity is generally decreased. Elevated CO₂ and NPK fertilization altered many of the factors known to influence aggregation, but did not affect water-stable aggregation at either depth, in any of the plant treatments. These results suggest that global changes will alter soil structure primarily due to shifts in vegetation composition.     

Denitrification in the top soil of managed grasslands in The Netherlands in relation to soil type and fertilizer level

The objective of this investigation was to determine how free-air carbon dioxide enrichment (FACE) of cotton (Gossypium hirsulam L.) affects root distribution in a natural soil environment. For two years cotton was grown on a Trix clay loam under two atmospheric CO₂ concentrations (370 and 550 μmol mol⁻¹) and two water treatments [wet, 100% of evapotranspiration (ET) replaced and dry, 75% (1990) and 67% (1991) of ET replaced] at Maricopa, AZ. At early vegetative and mid-reproductive growth, 90 cm soil cores were taken at 0,0.25, and 0.5 m perpendicular to row center; root variables were ascertained at three 30 cm depth increments. The effect of water stress alone or its interaction with CO₂ on measured variables during both samplings were rare and showed no consistent pattern. There was a significant CO₂ × position interaction for root length density at the vegetative stage (both years) and reproductive stage (1990 only); the positive effects of extra CO₂ were more evident at interrow positions (0.25 and 0.5 m). A CO₂ × depth × position interaction at the vegetative phase (1990) indicated that FACE increased root dry weight densities for the top soil depth increment at all positions and at the middle increment at the 0.5 m position. Similar trends were seen at the reproductive sampling for this measure as well as for root length density at both sample dates in 1990. In 1991, a CO₂ × depth interaction was noted at both periods; CO₂ enhancement of root densities (i.e., both length and dry weight) were observed within the upper and middle depths. Although variable in response, increases for root lineal density under high CO₂ were also seen. In general, results also revealed that the ambient CO₂ treatment had a higher proportion of its root system growing closer to the row center, both on a root length and dry wight basis. On the other hand, the FACE treatment had proportionately more of its roots allocated away from row center (root length basis only). Results from this field experiment clearly suggest that increased atmospheric CO₂ concentration will alter root distribution patterns in cotton.     

Root production and tissue quality in a shortgrass steppe exposed to elevated CO<Subscript>2</Subscript>: Using a new ingrowth method

A modified root ingrowth method was developed to minimize destructive sampling in experiments with limited space, and used to estimate belowground net primary production and root tissue quality in a native semiarid grassland exposed to elevated CO₂ for five years. Increases in root production of over 60% were observed with elevated CO₂ during years of intermediate levels of precipitation, with smaller effects in a very wet year and no effects in a very dry year. Aboveground to belowground production ratios, and the depth distribution of root production, did not differ between ambient and elevated CO₂ treatments. Root soluble concentrations increased an average of 11% and lignin concentrations decreased an average of 6% with elevated CO₂, while nitrogen concentrations decreased an average of 21%. However, most tissue quality responses to CO₂ varied greatly among years, and C:N ratios were higher in only one year (22 ambient vs. 33 elevated). Among years, root nitrogen concentrations declined with increasing aboveground plant nitrogen yield, and increased over the study period. Estimates of root production by the ingrowth donut method were much lower than previous estimates in the shortgrass steppe based on ¹⁴C decay. We discuss reasons why all ingrowth methods will always result in relative rather than absolute estimates of root production.     

Elevated atmospheric CO2 and feedback between carbon and nitrogen cycles

We tested a conceptual model describing the influence of elevated atmospheric CO₂ on plant production, soil microorganisms, and the cycling of C and N in the plant-soil system. Our model is based on the observation that in nutrient-poor soils, plants (C₃) grown in an elevated CO₂ atmosphere often increase production and allocation to belowground structures. We predicted that greater belowground C inputs at elevated CO₂ should elicit an increase in soil microbial biomass and increased rates of organic matter turnover and nitrogen availability. We measured photosynthesis, biomass production, and C allocation of Populus grandidentata Michx. grown in nutrient-poor soil for one field season at ambient and twice-ambient (i.e., elevated) atmospheric CO₂ concentrations. Plants were grown in a sandy subsurface soil i) at ambient CO₂ with no open top chamber, ii) at ambient CO₂ in an open top chamber, and iii) at twice-ambient CO₂ in an open top chamber. Plants were fertilized with 4.5 g N m⁻² over a 47 d period midway through the growing season. Following 152 d of growth, we quantified microbial biomass and the availabilities of C and N in rhizosphere and bulk soil. We tested for a significant CO₂ effect on plant growth and soil C and N dynamics by comparing the means of the chambered ambient and chambered elevated CO₂ treatments. Rates of photosynthesis in plants grown at elevated CO₂ were significantly greater than those measured under ambient conditions. The number of roots, root length, and root length increment were also substantially greater at elevated CO₂. Total and belowground biomass were significantly greater at elevated CO₂. Under N-limited conditions, plants allocated 50–70% of their biomass to roots. Labile C in the rhizosphere of elevated-grown plants was significantly greater than that measured in the ambient treatments; there were no significant differences between labile C pools in the bulk soil of ambient and elevated-grown plants. Microbial biomass C was significantly greater in the rhizosphere and bulk soil of plants grown at elevated CO₂ compared to that in the ambient treatment. Moreover, a short-term laboratory assay of N mineralization indicated that N availability was significantly greater in the bulk soil of the elevated-grown plants. Our results suggest that elevated atmospheric CO₂ concentrations can have a positive feedback effect on soil C and N dynamics producing greater N availability. Experiments conducted for longer periods of time will be necessary to test the potential for negative feedback due to altered leaf litter chemistry. ei]{gnH}{fnLambers} ei]{gnA C}{fnBorstlap}     

Competition for nitrogen between Pinus sylvestris and ectomycorrhizal fungi generates potential for negative feedback under elevated CO2

We investigated fungal species-specific responses of ectomycorrhizal (ECM) Scots pine (Pinus sylvestris) seedlings on growth and nutrient acquisition together with mycelial development under ambient and elevated CO₂. Each seedling was associated with one of the following ECM species: Hebeloma cylindrosporum, Laccaria bicolor, Suillus bovinus, S. luteus, Piloderma croceum, Paxillus involutus, Boletus badius, or non-mycorrhizal, under ambient, and elevated CO₂ (350 or 700 μl l⁻¹ CO₂); each treatment contained six replicates. The trial lasted 156 days. During the final 28 days, the seedlings were labeled with ¹⁴CO₂. We measured hyphal length, plant biomass, ¹⁴C allocation, and plant nitrogen and phosphorus concentration. Almost all parameters were significantly affected by fungal species and/or CO₂. There were very few significant interactions. Elevated CO₂ decreased shoot-to-root ratio, most strongly so in species with the largest extraradical mycelium. Under elevated CO₂, ECM root growth increased significantly more than hyphal growth. Extraradical hyphal length was significantly negatively correlated with shoot biomass, shoot N content, and total plant N uptake. Root dry weight was significantly negatively correlated with root N and P concentration. Fungal sink strength for N strongly affected plant growth through N immobilization. Mycorrhizal fungal-induced progressive nitrogen limitation (PNL) has the potential to generate negative feedback with plant growth under elevated CO₂. Responsible Editor: Herbert Johannes Kronzucker     

Photosynthetic pathway and ontogeny affect water relations and the impact of CO2 on Bouteloua gracilis (C4) and Pascopyrum smithii (C3)

The eastern Colorado shortgrass steppe is dominated by the C₄ grass, Bouteloua gracilis, but contains a mixture of C₃ grasses as well, including Pascopyrum smithii. Although the ecology of this region has been extensively studied, there is little information on how increasing atmospheric CO₂ will affect it. This growth chamber study investigated gas exchange, water relations, growth, and biomass and carbohydrate partitioning in B. gracilis and P. smithii grown under present ambient and elevated CO₂ concentrations of 350 μl l⁻¹and 700 μl l⁻¹, respectively, and two deficit irrigation regimes. The experiment was conducted in soil-packed columns planted to either species over a 2-month period under summer-like conditions and with no fertilizer additions. Our objective was to better understand how these species and the functional groups they represent will respond in future CO₂-enriched environments. Leaf CO₂ assimilation (A _n), transpiration use efficiency (TUE, or A _n/transpiration), plant growth, and whole-plant water use efficiency (WUE, or plant biomass production/water evapotranspired) of both species were greater at elevated CO₂, although responses were more pronounced for P. smithii. Elevated CO₂ enhanced photosynthesis, TUE, and growth in both species through higher soil water content (SWC) and leaf water potentials (Ψ) and stimulation of photosynthesis. Consumptive water use was greater and TUE less for P. smithii than B. gracilis during early growth when soil water was more available. Declining SWC with time was associated with a steadily increased sequestering of total non-structural carbohydrates (TNCs), storage carbohydrates (primarily fructans for P. smithii) and biomass in belowground organs of P. smithii, but not B. gracilis. The root:shoot ratio of P. smithii also increased at elevated CO₂, while the root:shoot ratio of B. gracilis was unresponsive to CO₂. These partitioning responses may be the consequence of different ontogenetic strategies of a cool-season and warm-season grass entering a warm, dry summer period; the cool-season P. smithii responds by sequestering TNCs belowground in preparation for summer dormancy, while resource partitioning of the warm-season B. gracilis remains unaltered. One consequence of greater partitioning of resources into P. smithii belowground organs in the present study was maintenance of higher Ψ and A _n rates. This, along with differences in photosynthetic pathway, may have accounted for the greater responsiveness of P. smithii to CO₂ enrichment compared to B. gracilis. Received: 21 July 1997 / Accepted: 16 December 1997