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1.
Soil CO2 efflux was measured in clear‐cut and intact plots in order to quantify the impact of harvest on soil respiration in an intensively managed Eucalyptus plantation, and to evaluate the increase in heterotrophic component of soil respiration because of the decomposition of harvest residues. Soil CO2 effluxes showed a pronounced seasonal trend, which was well related to the pattern of precipitation and soil water content and were always significantly lower in the clear‐cut plots than in the intact plots. On an annual basis, soil respiration represented 1.57 and 0.91 kgC m?2 yr?1 in intact and clear‐cut plots, respectively. During the first year following harvest, residues have lost 0.79 kgC m?2 yr?1. Our estimate of heterotrophic respiration was calculated assuming that it was similar to soil respiration in the clear‐cut area except that the decomposition of residues did not occur, and it was further corrected for differences in soil water content between intact and clear‐cut plots and for the cessation of leaf and fine root turnover in clear cut. Heterotrophic respiration in clear‐cut plots was estimated at 1.18 kgC m?2 yr?1 whereas it was only 0.65 kgC m?2 yr?1 in intact plots (41% of soil respiration). Assumptions and uncertainties with these calculations are discussed.  相似文献   

2.
We investigated the effects of elevated atmospheric CO2 concentrations (ambient + 200 ppm) on fine root production and soil carbon dynamics in a loblolly pine (Pinus taeda) forest subject to free‐air CO2 enrichment (FACE) near Durham, NC (USA). Live fine root mass (LFR) showed less seasonal variation than dead fine root mass (DFR), which was correlated with seasonal changes in soil moisture and soil temperature. LFR mass increased significantly (by 86%) in the elevated CO2 treatment, with an increment of 37 g(dry weight) m?2 above the control plots after two years of CO2 fumigation. There was no long‐term increment in DFR associated with elevated CO2, but significant seasonal accumulations of DFR mass occurred during the summer of the second year of fumigation. Overall, root net primary production (RNPP) was not significantly different, but annual carbon inputs were 21.7 gC m?2 y?1 (68%) higher in the elevated CO2 treatment compared to controls. Specific root respiration was not altered by the CO2 treatment during most of the year; however, it was significantly higher by 21% and 13% in September 1997 and May 1998, respectively, in elevated CO2. We did not find statistically significant differences in the C/N ratio of the root tissue, root decomposition or phosphatase activity in soil and roots associated with the treatment. Our data show that the early response of a loblolly pine forest ecosystem subject to CO2 enrichment is an increase in its fine root population and a trend towards higher total RNPP after two years of CO2 fumigation.  相似文献   

3.
Chronic N additions to forest ecosystems can enhance soil N availability, potentially leading to reduced C allocation to root systems. This in turn could decrease soil CO2 efflux. We measured soil respiration during the first, fifth, sixth and eighth years of simulated atmospheric NO3? deposition (3 g N m?2 yr?1) to four sugar maple‐dominated northern hardwood forests in Michigan to assess these possibilities. During the first year, soil respiration rates were slightly, but not significantly, higher in the NO3?‐amended plots. In all subsequent measurement years, soil respiration rates from NO3?‐amended soils were significantly depressed. Soil temperature and soil matric potential were measured concurrently with soil respiration and used to develop regression relationships for predicting soil respiration rates. Estimates of growing season and annual soil CO2 efflux made using these relationships indicate that these C fluxes were depressed by 15% in the eighth year of chronic NO3? additions. The decrease in soil respiration was not due to reduced C allocation to roots, as root respiration rates, root biomass, and root turnover were not significantly affected by N additions. Aboveground litter also was unchanged by the 8 years of treatment. Of the remaining potential causes for the decline in soil CO2 efflux, reduced microbial respiration appears to be the most likely possibility. Documented reductions in microbial biomass and the activities of extracellular enzymes used for litter degradation on the NO3?‐amended plots are consistent with this explanation.  相似文献   

4.
Fine roots (≤1 mm diameter) are critical in plant water and nutrient absorption, and it is important to understand how rising atmospheric CO2 will affect them as part of terrestrial ecosystem responses to global change. This study's objective was to determine the effects of elevated CO2 on production, mortality, and standing crops of fine root length over 2 years in a free‐air CO2 enrichment (FACE) facility in the Mojave Desert of southern Nevada, USA. Three replicate 25 m diameter FACE rings were maintained at ambient (~370 μmol mol?1) and elevated CO2 (~550 μmol mol?1) atmospheric concentrations. Twenty‐eight minirhizotron tubes were placed in each ring to sample three microsite locations: evergreen Larrea shrubs, drought‐deciduous Ambrosia shrubs, and along systematic community transects (primarily in shrub interspaces which account for ~85% of the area). Seasonal dynamics were similar for ambient and elevated CO2: fine root production peaked in April–June, with peak standing crop occurring about 1 month later, and peak mortality occurring during the hot summer months, with higher values for all three measures in a wet year compared with a dry year. Fine root standing crop, production, and mortality were not significantly different between treatments except standing crop along community transects, where fine root length was significantly lower in elevated CO2. Fine root turnover (annual cumulative mortality/mean standing crop) ranged from 2.33 to 3.17 year?1, and was not significantly different among CO2 treatments, except for community transect tubes where it was significantly lower for elevated CO2. There were no differences in fine root responses to CO2 between evergreen (Larrea) and drought‐deciduous (Ambrosia) shrubs. Combined with observations of increased leaf‐level water‐use efficiency and lack of soil moisture differences, these results suggest that under elevated CO2 conditions, reduced root systems (compared with ambient CO2) appear sufficient to provide resources for modest aboveground production increases across the community, but in more fertile shrub microsites, fine root systems of comparable size with those in ambient CO2 were required to support the greater aboveground production increases. For community transects, development of the difference in fine root standing crops occurred primarily through lower stimulation of fine root production in the elevated CO2 treatment during periods of high water availability.  相似文献   

5.
Elevated atmospheric carbon dioxide increases soil carbon   总被引:4,自引:0,他引:4  
The general lack of significant changes in mineral soil C stocks during CO2‐enrichment experiments has cast doubt on predictions that increased soil C can partially offset rising atmospheric CO2 concentrations. Here, we show, through meta‐analysis techniques, that these experiments collectively exhibited a 5.6% increase in soil C over 2–9 years, at a median rate of 19 g C m?2 yr?1. We also measured C accrual in deciduous forest and grassland soils, at rates exceeding 40 g C m?2 yr?1 for 5–8 years, because both systems responded to CO2 enrichment with large increases in root production. Even though native C stocks were relatively large, over half of the accrued C at both sites was incorporated into microaggregates, which protect C and increase its longevity. Our data, in combination with the meta‐analysis, demonstrate the potential for mineral soils in diverse temperate ecosystems to store additional C in response to CO2 enrichment.  相似文献   

6.
Response of soil respiration (CO2 emission) to simulated nitrogen (N) deposition in a mature tropical forest in southern China was studied from October 2005 to September 2006. The objective was to test the hypothesis that N addition would reduce soil respiration in N saturated tropical forests. Static chamber and gas chromatography techniques were used to quantify the soil respiration, following four‐levels of N treatments (Control, no N addition; Low‐N, 5 g N m?2 yr?1; Medium‐N, 10 g N m?2 yr?1; and High‐N, 15 g N m?2 yr?1 experimental inputs), which had been applied for 26 months before and continued throughout the respiration measurement period. Results showed that soil respiration exhibited a strong seasonal pattern, with the highest rates found in the warm and wet growing season (April–September) and the lowest rates in the dry dormant season (December–February). Soil respiration rates showed a significant positive exponential relationship with soil temperature, whereas soil moisture only affect soil respiration at dry conditions in the dormant season. Annual accumulative soil respiration was 601±30 g CO2‐C m?2 yr?1 in the Controls. Annual mean soil respiration rate in the Control, Low‐N and Medium‐N treatments (69±3, 72±3 and 63±1 mg CO2‐C m?2 h?1, respectively) did not differ significantly, whereas it was 14% lower in the High‐N treatment (58±3 mg CO2‐C m?2 h?1) compared with the Control treatment, also the temperature sensitivity of respiration, Q10 was reduced from 2.6 in the Control with 2.2 in the High‐N treatment. The decrease in soil respiration occurred in the warm and wet growing season and were correlated with a decrease in soil microbial activities and in fine root biomass in the N‐treated plots. Our results suggest that response of soil respiration to atmospheric N deposition in tropical forests is a decline, but it may vary depending on the rate of N deposition.  相似文献   

7.
Elevated atmospheric carbon dioxide (CO2) often stimulates the growth of fine roots, yet there are few reports of responses of intact root systems to long‐term CO2 exposure. We investigated the effects of elevated CO2 on fine root growth using open top chambers in a scrub oak ecosystem at Kennedy Space Center, Florida for more than 7 years. CO2 enrichment began immediately after a controlled burn, which simulated the natural disturbance that occurs in this system every 10–15 years. We hypothesized that (1) root abundance would increase in both treatments as the system recovered from fire; (2) elevated CO2 would stimulate root growth; and (3) elevated CO2 would alter root distribution. Minirhizotron tubes were used to measure fine root length density (mm cm?2) every three months. During the first 2 years after fire recovery, fine root abundance increased in all treatments and elevated CO2 significantly enhanced root abundance, causing a maximum stimulation of 181% after 20 months. The CO2 stimulation was initially more pronounced in the top 10 cm and 38–49 cm below the soil surface. However, these responses completely disappeared during the third year of experimental treatment: elevated CO2 had no effect on root abundance or on the depth distribution of fine roots during years 3–7. The results suggest that, within a few years following fire, fine roots in this scrub oak ecosystem reach closure, defined here as a dynamic equilibrium between production and mortality. These results further suggest that elevated CO2 hastens root closure but does not affect maximum root abundance. Limitation of fine root growth by belowground resources – particularly nutrients in this nutrient‐poor soil – may explain the transient response to elevated CO2.  相似文献   

8.
Fine root dynamics have the potential to contribute significantly to ecosystem‐scale biogeochemical cycling, including the production and emission of greenhouse gases. This is particularly true in tropical forests which are often characterized as having large fine root biomass and rapid rates of root production and decomposition. We examined patterns in fine root dynamics on two soil types in a lowland moist Amazonian forest, and determined the effect of root decay on rates of C and N trace gas fluxes. Root production averaged 229 (±35) and 153 (±27) g m?2 yr?1 for years 1 and 2 of the study, respectively, and did not vary significantly with soil texture. Root decay was sensitive to soil texture with faster rates in the clay soil (k=?0.96 year?1) than in the sandy loam soil (k=?0.61 year?1), leading to greater standing stocks of dead roots in the sandy loam. Rates of nitrous oxide (N2O) emissions were significantly greater in the clay soil (13±1 ng N cm?2 h?1) than in the sandy loam (1.4±0.2 ng N cm?2 h?1). Root mortality and decay following trenching doubled rates of N2O emissions in the clay and tripled them in sandy loam over a 1‐year period. Trenching also increased nitric oxide fluxes, which were greater in the sandy loam than in the clay. We used trenching (clay only) and a mass balance approach to estimate the root contribution to soil respiration. In clay soil root respiration was 264–380 g C m?2 yr?1, accounting for 24% to 35% of the total soil CO2 efflux. Estimates were similar using both approaches. In sandy loam, root respiration rates were slightly higher and more variable (521±206 g C m2 yr?1) and contributed 35% of the total soil respiration. Our results show that soil heterotrophs strongly dominate soil respiration in this forest, regardless of soil texture. Our results also suggest that fine root mortality and decomposition associated with disturbance and land‐use change can contribute significantly to increased rates of nitrogen trace gas emissions.  相似文献   

9.
Soil fungi couple plant and ecosystem resource demands to pools of soil resources. Research on these organisms is needed to predict how rising atmospheric CO2 will influence forest ecosystem processes and soil carbon (C) sequestration potential. We examined the influence of free‐air‐CO2‐enrichment (FACE) on mycorrhizal and extraradical rhizomorph dynamics over a 5‐year period in a loblolly pine forest using minirhizotrons. Standing crop of mycorrhizal root tips varied greatly spatially and through time. Summed across all years, CO2 enrichment increased mycorrhizal root tip production by 194% in deep soil (15–30 cm) but did not influence mycorrhizal production in shallow soil (0–15 cm). Production and mortality of soil rhizomorph length was 27% and 25% greater in CO2‐enriched plots compared with controls over a 5‐year period beginning in January of 2000 and running through autumn 2004. Effects of atmospheric CO2 enrichment on longevity of mycorrhizal root tips and rhizomorphs varied with soil depth (mycorrhizae and rhizomorphs) and with diameter (rhizomorphs). For instance, survival of mycorrhizal tips was reduced in CO2‐enriched plots in deep soil (15–30 cm depth) but was increased in shallower soil (0–15 cm). Rhizomorph turnover was accelerated in shallow soil but effects on survivorship in deep soil varied according to diameter. A drought in 2002 coupled with loss of leaf area to an ice storm late in 2002 were followed by reductions in rhizomorph and mycorrhizal production, increases in mortality, and decreases in standing crop during 2003 and 2004. These effects tended to be more severe in CO2‐enriched plots. Positive effects of atmospheric CO2 enrichment on mycorrhizal fungi, primarily observed in deeper soil, are probably contributing to the prolonged stimulation of NPP by CO2 enrichment at the Duke FACE study site.  相似文献   

10.
The long‐term effects of conservation management practices on greenhouse gas fluxes from tropical/subtropical croplands remain to be uncertain. Using both manual and automatic sampling chambers, we measured N2O and CH4 fluxes at a long‐term experimental site (1968–present) in Queensland, Australia from 2006 to 2009. Annual net greenhouse gas fluxes (NGGF) were calculated from the 3‐year mean N2O and CH4 fluxes and the long‐term soil organic carbon changes. N2O emissions exhibited clear daily, seasonal and interannual variations, highlighting the importance of whole‐year measurement over multiple years for obtaining temporally representative annual emissions. Averaged over 3 years, annual N2O emissions from the unfertilized and fertilized soils (90 kg N ha?1 yr?1 as urea) amounted to 138 and 902 g N ha?1, respectively. The average annual N2O emissions from the fertilized soil were 388 g N ha?1 lower under no‐till (NT) than under conventional tillage (CT) and 259 g N ha?1 higher under stubble retention (SR) than under stubble burning (SB). Annual N2O emissions from the unfertilized soil were similar between the contrasting tillage and stubble management practices. The average emission factors of fertilizer N were 0.91%, 1.20%, 0.52% and 0.77% for the CT‐SB, CT‐SR, NT‐SB and NT‐SR treatments, respectively. Annual CH4 fluxes from the soil were very small (?200–300 g CH4 ha?1 yr?1) with no significant difference between treatments. The NGGF were 277–350 kg CO2‐e ha?1 yr?1 for the unfertilized treatments and 401–710 kg CO2‐e ha?1 yr?1 for the fertilized treatments. Among the fertilized treatments, N2O emissions accounted for 52–97% of NGGF and NT‐SR resulted in the lowest NGGF (401 kg CO2‐e ha?1 yr?1 or 140 kg CO2‐e t?1 grain). Therefore, NT‐SR with improved N fertilizer management practices was considered the most promising management regime for simultaneously achieving maximal yield and minimal NGGF.  相似文献   

11.
Elevated atmospheric CO2 concentration may result in increased below‐ground carbon allocation by trees, thereby altering soil carbon cycling. Seasonal estimates of soil surface carbon flux were made to determine whether carbon losses from Pinus radiata trees growing at elevated CO2 concentration were higher than those at ambient CO2 concentration, and whether this was related to increased fine root growth. Monthly soil surface carbon flux density (f) measurements were made on plots with trees growing at ambient (350) and elevated (650 μmol mol?1) CO2 concentration in large open‐top chambers. Prior to planting the soil carbon concentration (0.1%) and f (0.28 μmol m?2 s?1 at 15 °C) were low. A function describing the radial pattern of f with distance from tree stems was used to estimate the annual carbon flux from tree plots. Seasonal estimates of fine root production were made from minirhizotrons and the radial distribution of roots compared with radial measurements of f. A one‐dimensional gas diffusion model was used to estimate f from soil CO2 concentrations at four depths. For the second year of growth, the annual carbon flux from the plots was 1671 g y?1 and 1895 g y?1 at ambient and elevated CO2 concentrations, respectively, although this was not a significant difference. Higher f at elevated CO2 concentration was largely explained by increased fine root biomass. Fine root biomass and stem production were both positively related to f. Both root length density and f declined exponentially with distance from the stem, and had similar length scales. Diurnal changes in f were largely explained by changes in soil temperature at a depth of 0.05 m. Ignoring the change of f with increasing distance from tree stems when scaling to a unit ground area basis from measurements with individual trees could result in under‐ or overestimates of soil‐surface carbon fluxes, especially in young stands when fine roots are unevenly distributed.  相似文献   

12.
Responses of alpine tree line ecosystems to increasing atmospheric CO2 concentrations and global warming are poorly understood. We used an experiment at the Swiss tree line to investigate changes in vegetation biomass after 9 years of free air CO2 enrichment (+200 ppm; 2001–2009) and 6 years of soil warming (+4 °C; 2007–2012). The study contained two key tree line species, Larix decidua and Pinus uncinata, both approximately 40 years old, growing in heath vegetation dominated by dwarf shrubs. In 2012, we harvested and measured biomass of all trees (including root systems), above‐ground understorey vegetation and fine roots. Overall, soil warming had clearer effects on plant biomass than CO2 enrichment, and there were no interactive effects between treatments. Total plant biomass increased in warmed plots containing Pinus but not in those with Larix. This response was driven by changes in tree mass (+50%), which contributed an average of 84% (5.7 kg m?2) of total plant mass. Pinus coarse root mass was especially enhanced by warming (+100%), yielding an increased root mass fraction. Elevated CO2 led to an increased relative growth rate of Larix stem basal area but no change in the final biomass of either tree species. Total understorey above‐ground mass was not altered by soil warming or elevated CO2. However, Vaccinium myrtillus mass increased with both treatments, graminoid mass declined with warming, and forb and nonvascular plant (moss and lichen) mass decreased with both treatments. Fine roots showed a substantial reduction under soil warming (?40% for all roots <2 mm in diameter at 0–20 cm soil depth) but no change with CO2 enrichment. Our findings suggest that enhanced overall productivity and shifts in biomass allocation will occur at the tree line, particularly with global warming. However, individual species and functional groups will respond differently to these environmental changes, with consequences for ecosystem structure and functioning.  相似文献   

13.
Soil‐surface CO2 efflux and its spatial and temporal variations were examined in an 8‐y‐old ponderosa pine plantation in the Sierra Nevada Mountains in California from June 1998 to August 1999. Continuous measurements of soil CO2 efflux, soil temperatures and moisture were conducted on two 20 × 20 m sampling plots. Microbial biomass, fine root biomass, and the physical and chemical properties of the soil were also measured at each of the 18 sampling locations on the plots. It was found that the mean soil CO2 efflux in the plantation was 4.43 µmol m?2 s?1 in the growing season and 3.12 µmol m?2 s?1 in the nongrowing season. These values are in the upper part of the range of published soil‐surface CO2 efflux data. The annual maximum and minimum CO2 efflux were 5.87 and 1.67 µmol m?2 s?1, respectively, with the maximum occurring between the end of May and early June and the minimum in December. The diurnal fluctuation of CO2 efflux was relatively small (< 20%) with the minimum appearing around 09.00 hours and the maximum around 14.00 hours. Using daytime measurements of soil CO2 efflux tends to overestimate the daily mean soil CO2 efflux by 4–6%. The measurements taken between 09.00 and 11.00 hours (local time) seem to better represent the daily mean with a reduced sampling error of 0.9–1.5%. The spatial variation of soil CO2 efflux among the 18 sampling points was high, with a coefficient of variation of approximately 30%. Most (84%) of the spatial variation was explained by fine root biomass, microbial biomass, and soil physical and chemical properties. Although soil temperature and moisture explained most of the temporal variations (76–95%) of soil CO2 efflux, the two variables together explained less than 34% of the spatial variation. Microbial biomass, fine root biomass, soil nitrogen content, organic matter content, and magnesium content were significantly and positively correlated with soil CO2 efflux, whereas bulk density and pH value were negatively correlated with CO2 efflux. The relationship between soil CO2 efflux and soil temperature was significantly controlled by soil moisture with a Q10 value of 1.4 when soil moisture was <14% and 1.8 when soil moisture was >14%. Understanding the spatial and temporal variations is essential to accurately assessment of carbon budget at whole ecosystem and landscape scales. Thus, this study bears important implications for the study of large‐scale ecosystem dynamics, particularly in response to climatic variations and management regimes.  相似文献   

14.
free air carbon dioxide enrichment (FACE) and open top chamber (OTC) studies are valuable tools for evaluating the impact of elevated atmospheric CO2 on nutrient cycling in terrestrial ecosystems. Using meta‐analytic techniques, we summarized the results of 117 studies on plant biomass production, soil organic matter dynamics and biological N2 fixation in FACE and OTC experiments. The objective of the analysis was to determine whether elevated CO2 alters nutrient cycling between plants and soil and if so, what the implications are for soil carbon (C) sequestration. Elevated CO2 stimulated gross N immobilization by 22%, whereas gross and net N mineralization rates remained unaffected. In addition, the soil C : N ratio and microbial N contents increased under elevated CO2 by 3.8% and 5.8%, respectively. Microbial C contents and soil respiration increased by 7.1% and 17.7%, respectively. Despite the stimulation of microbial activity, soil C input still caused soil C contents to increase by 1.2% yr?1. Namely, elevated CO2 stimulated overall above‐ and belowground plant biomass by 21.5% and 28.3%, respectively, thereby outweighing the increase in CO2 respiration. In addition, when comparing experiments under both low and high N availability, soil C contents (+2.2% yr?1) and above‐ and belowground plant growth (+20.1% and+33.7%) only increased under elevated CO2 in experiments receiving the high N treatments. Under low N availability, above‐ and belowground plant growth increased by only 8.8% and 14.6%, and soil C contents did not increase. Nitrogen fixation was stimulated by elevated CO2 only when additional nutrients were supplied. These results suggest that the main driver of soil C sequestration is soil C input through plant growth, which is strongly controlled by nutrient availability. In unfertilized ecosystems, microbial N immobilization enhances acclimation of plant growth to elevated CO2 in the long‐term. Therefore, increased soil C input and soil C sequestration under elevated CO2 can only be sustained in the long‐term when additional nutrients are supplied.  相似文献   

15.
Willow coppice, energy maize and Miscanthus were evaluated regarding their soil‐derived trace gas emission potential involving a nonfertilized and a crop‐adapted slow‐release nitrogen (N) fertilizer scheme. The N application rate was 80 kg N ha?1 yr?1 for the perennial crops and 240 kg N ha?1 yr?1 for the annual maize. A replicated field experiment was conducted with 1‐year measurements of soil fluxes of CH4, CO2 and N2O in weekly intervals using static chambers. The measurements revealed a clear seasonal trend in soil CO2 emissions, with highest emissions being found for the N‐fertilized Miscanthus plots (annual mean: 50 mg C m?² h?1). Significant differences between the cropping systems were found in soil N2O emissions due to their dependency on amount and timing of N fertilization. N‐fertilized maize plots had highest N2O emissions by far, which accumulated to 3.6 kg N2O ha?1 yr?1. The contribution of CH4 fluxes to the total soil greenhouse gas subsumption was very small compared with N2O and CO2. CH4 fluxes were mostly negative indicating that the investigated soils mainly acted as weak sinks for atmospheric CH4. To identify the system providing the best ratio of yield to soil N2O emissions, a subsumption relative to biomass yields was calculated. N‐fertilized maize caused the highest soil N2O emissions relative to dry matter yields. Moreover, unfertilized maize had higher relative soil N2O emissions than unfertilized Miscanthus and willow. These results favour perennial crops for bioenergy production, as they are able to provide high yields with low N2O emissions in the field.  相似文献   

16.
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.  相似文献   

17.
Eddy covariance was used to measure the net CO2 exchange (NEE) over ecosystems differing in land use (forest and agriculture) in Thuringia, Germany. Measurements were carried out at a managed, even‐aged European beech stand (Fagus sylvatica, 70–150 years old), an unmanaged, uneven‐aged mixed beech stand in a late stage of development (F. sylvatica, Fraxinus excelsior, Acer pseudoplantanus, and other hardwood trees, 0–250 years old), a managed young Norway spruce stand (Picea abies, 50 years old), and an agricultural field growing winter wheat in 2001, and potato in 2002. Large contrasts were found in NEE rates between the land uses of the ecosystems. The managed and unmanaged beech sites had very similar net CO2 uptake rates (~?480 to ?500 g C m?2 yr?1). Main differences in seasonal NEE patterns between the beech sites were because of a later leaf emergence and higher maximum leaf area index at the unmanaged beech site, probably as a result of the species mix at the site. In contrast, the spruce stand had a higher CO2 uptake in spring but substantially lower net CO2 uptake in summer than the beech stands. This resulted in a near neutral annual NEE (?4 g C m?2 yr?1), mainly attributable to an ecosystem respiration rate almost twice as high as that of the beech stands, despite slightly lower temperatures, because of the higher elevation. Crops in the agricultural field had high CO2 uptake rates, but growing season length was short compared with the forest ecosystems. Therefore, the agricultural land had low‐to‐moderate annual net CO2 uptake (?34 to ?193 g C m?2), but with annual harvest taken into account it will be a source of CO2 (+97 to +386 g C m?2). The annually changing patchwork of crops will have strong consequences on the regions' seasonal and annual carbon exchange. Thus, not only land use, but also land‐use history and site‐specific management decisions affect the large‐scale carbon balance.  相似文献   

18.
We present the annual patterns of net ecosystem‐atmosphere exchange (NEE) of CO2 and H2O observed from a 447 m tall tower sited within a mixed forest in northern Wisconsin, USA. The methodology for determining NEE from eddy‐covariance flux measurements at 30, 122 and 396 m above the ground, and from CO2 mixing ratio measurements at 11, 30, 76, 122, 244 and 396 m is described. The annual cycle of CO2 mixing ratio in the atmospheric boundary layer (ABL) is also discussed, and the influences of local NEE and large‐scale advection are estimated. During 1997 gross ecosystem productivity (947?18 g C m?2 yr?1), approximately balanced total ecosystem respiration (963±19 g C m?2 yr?1), and NEE of CO2 was close to zero (16±19 g C m?2 yr?1 emitted into the atmosphere). The error bars represent the standard error of the cumulative daily NEE values. Systematic errors are also assessed. The identified systematic uncertainties in NEE of CO2 are less than 60 g C m?2 yr?1. The seasonal pattern of NEE of CO2 was highly correlated with leaf‐out and leaf‐fall, and soil thaw and freeze, and was similar to purely deciduous forest sites. The mean daily NEE of CO2 during the growing season (June through August) was ?1.3 g C m?2 day?1, smaller than has been reported for other deciduous forest sites. NEE of water vapor largely followed the seasonal pattern of NEE of CO2, with a lag in the spring when water vapor fluxes increased before CO2 uptake. In general, the Bowen ratios were high during the dormant seasons and low during the growing season. Evapotranspiration normalized by potential evapotranspiration showed the opposite pattern. The seasonal course of the CO2 mixing ratio in the ABL at the tower led the seasonal pattern of NEE of CO2 in time: in spring, CO2 mixing ratios began to decrease prior to the onset of daily net uptake of CO2 by the forest, and in fall mixing ratios began to increase before the forest became a net source for CO2 to the atmosphere. Transport as well as local NEE of CO2 are shown to be important components of the ABL CO2 budget at all times of the year.  相似文献   

19.
Observed responses of upland‐oak vegetation of the eastern deciduous hardwood forest to changing CO2, temperature, precipitation and tropospheric ozone (O3) were derived from field studies and interpreted with a stand‐level model for an 11‐year range of environmental variation upon which scenarios of future environmental change were imposed. Scenarios for the year 2100 included elevated [CO2] and [O3] (+385 ppm and +20 ppb, respectively), warming (+4°C), and increased winter precipitation (+20% November–March). Simulations were run with and without adjustments for experimentally observed physiological and biomass adjustments. Initial simplistic model runs for single‐factor changes in CO2 and temperature predicted substantial increases (+191% or 508 g C m?2 yr?1) or decreases (?206% or ?549 g C m?2 yr?1), respectively, in mean annual net ecosystem carbon exchange (NEEa≈266±23 g C m?2 yr?1 from 1993 to 2003). Conversely, single‐factor changes in precipitation or O3 had comparatively small effects on NEEa (0% and ?35%, respectively). The combined influence of all four environmental changes yielded a 29% reduction in mean annual NEEa. These results suggested that future CO2‐induced enhancements of gross photosynthesis would be largely offset by temperature‐induced increases in respiration, exacerbation of water deficits, and O3‐induced reductions in photosynthesis. However, when experimentally observed physiological adjustments were included in the simulations (e.g. acclimation of leaf respiration to warming), the combined influence of the year 2100 scenario resulted in a 20% increase in NEEa not a decrease. Consistent with the annual model's predictions, simulations with a forest succession model run for gradually changing conditions from 2000 to 2100 indicated an 11% increase in stand wood biomass in the future compared with current conditions. These model‐based analyses identify critical areas of uncertainty for multivariate predictions of future ecosystem response, and underscore the importance of long term field experiments for the evaluation of acclimation and growth under complex environmental scenarios.  相似文献   

20.
Elevated CO2 concentrations generally stimulate grassland productivity, but herbaceous plants have only a limited capacity to sequester extra carbon (C) in biomass. However, increased primary productivity under elevated CO2 could result in increased transfer of C into soils where it could be stored for prolonged periods and exercise a negative feedback on the rise in atmospheric CO2. Measuring soil C sequestration directly is notoriously difficult for a number of methodological reasons. Here, we present a method that combines C isotope labelling with soil C cycle modelling to partition net soil sequestration into changes in new C fixed over the experimental duration (Cnew) and pre‐experimental C (Cold). This partitioning is advantageous because the Cnew accumulates whereas Cold is lost in the course of time (ΔCnew>0 whereas ΔCold<0). We applied this method to calcareous grassland exposed to 600 μL CO2 L?1 for 6 years. The CO2 used for atmospheric enrichment was depleted in 13C relative to the background atmosphere, and this distinct isotopic signature was used to quantify net soil Cnew fluxes under elevated CO2. Using 13C/12C mass balance and inverse modelling, the Rothamsted model ‘RothC’ predicted gross soil Cnew inputs under elevated CO2 and the decomposition of Cold. The modelled soil C pools and fluxes were in good agreement with experimental data. C isotope data indicated a net sequestration of ≈90 g Cnew m?2 yr?1 in elevated CO2. Accounting for Cold‐losses, this figure was reduced to ≈30 g C m?2 yr?1 at elevated CO2; the elevated CO2‐effect on net C sequestration was in the range of≈10 g C m?2 yr?1. A sensitivity and error analysis suggests that the modelled data are relatively robust. However, elevated CO2‐specific mechanisms may necessitate a separate parameterization at ambient and elevated CO2; these include increased soil moisture due to reduced leaf conductance, soil disaggregation as a consequence of increased soil moisture, and priming effects. These effects could accelerate decomposition of Cold in elevated CO2 so that the CO2 enrichment effect may be zero or even negative. Overall, our findings suggest that the C sequestration potential of this grassland under elevated CO2 is rather limited.  相似文献   

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