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1.
Forest fragmentation in tropical ecosystems can alter nutrient cycling in diverse ways. We have analysed the effects of the forest-pasture edge on nutrient soil dynamics in a tropical deciduous forest (TDF) in Mexico. In two remnant forest fragments, both larger than 10 ha, litterfall, litter and soil samples associated to the tree Caesalpinia eriostachys were collected at five distances from the pasture edge into the inner forest (10 m in the pasture and 0–10, 30–40, 70–80 and 100–110 m towards the forest interior). We measured the concentrations of carbon (C), nitrogen (N) and phosphorus (P) in litterfall, surface litter and soil, and soil microbial C (Cmic) and microbial N (Nmic). Soil nutrient concentrations and Cmic and Nmic were lower in the pasture soils than in the forest soil samples. Total C and N pools, and Cmic and Nmic in the pasture were lower than in the forest. In contrast, net N immobilization and the increase in Nmic from rain to dry season increased from the edge to the inner forest. Soil P concentration was lower in the pasture and at the first distance class in the forest margin (0–10 m) than in the sites located further into the forest, while litter P concentration had the inverse pattern. Litterfall P was also reduced near the edge and increased towards the forest interior. As a consequence, litterfall C:P and N:P ratios decreased from the edge to the inner forest. These results suggest that the forest–pasture edge disrupts P dynamics within the first 10 m in the forest. Thus, plants' use of nutrients and productivity could be altered in the edge of fragmented forests.  相似文献   

2.
Large seasonal changes in Q10 of soil respiration in a beech forest   总被引:1,自引:0,他引:1  
We analyzed one year of continuous soil respiration measurements to assess variations in the temperature sensitivity of soil respiration at a Danish beech forest. A single temperature function derived from all measurements across the year (Q10 = 4.2) was adequate for estimating the total annual soil respiration and its seasonal evolution. However, Q10's derived from weekly datasets ranged between three in summer (at a mean soil temperature of 14 °C) and 23 in winter (at 2 °C), indicating that the annual temperature function underestimated the synoptic variations in soil respiration during winter. These results highlight that empirical models should be parameterized at a time resolution similar to that required by the output of the model. If the objective of the model is to simulate the total annual soil respiration rate, annual parameterization suffices. If however, soil respiration needs to be simulated over time periods from days to weeks, as is the case when soil respiration is compared to total ecosystem respiration during synoptic weather patterns, more short‐term parameterization is required. Despite the higher wintertime Q10's, the absolute response of soil respiration to temperature was smaller in winter than in summer. This is mainly because in absolute numbers, the temperature sensitivity of soil respiration depends not only on Q10, but also on the rate of soil respiration, which is highly reduced in winter. Nonetheless, the Q10 of soil respiration in winter was larger than can be explained by the decreasing respiration rate only. Because the seasonal changes in Q10 were negatively correlated with temperature and positively correlated with soil moisture, they could also be related to changing temperature and/or soil moisture conditions.  相似文献   

3.
Soil respiration (SR) represents a major component of forest ecosystem respiration and is influenced seasonally by environmental factors such as temperature, soil moisture, root respiration, and litter fall. Changes in these environmental factors correspond with shifts in plant phenology. In this study, we examined the relationship between canopy phenophases (pre-growth, growth, pre-dormancy, and dormancy) and SR sensitivity to changes in soil temperature (TS). SR was measured 53 times over 550 days within an oak forest in northwest Ohio, USA. Annual estimates of SR were calculated with a Q10 model based on TS on a phenological (PT), or annual timescale (AT), or TS and soil volumetric water content (VWC) on a phenological (PTM) or annual (ATM) timescale. We found significant (p<0.01) difference in apparent Q10 from year 2004 (1.23) and year 2005 (2.76) during the growth phenophase. Accounting for moisture-sensitivity increased model performance compared to temperature-only models: the error was −17% for the ATM model and −6% for the PTM model. The annual models consistently underestimated SR in summer and overestimated it in winter. These biases were reduced by delineating SR by tree phenophases and accounting for variation in soil moisture. Even though the bias of annual models in winter SR was small in absolute scale, the relative error was about 91%, and may thus have significant implications for regional and continental C balance estimates.  相似文献   

4.
Tropical soils account for 10%–20% of the 15–35 Tg of atmospheric methane (CH4) consumed annually by soils, although tropical deforestation could be changing the soil sink. The objectives of this study were (a) to quantify differences in soil CH4 fluxes among primary forest, secondary forest, active pasture, and degraded pasture in eastern Amazonia; and (b) to investigate controlling mechanisms of CH4 fluxes, including N availability, gas-phase transport, and soil respiration. At one ranch, Fazenda Vitória, annual uptake estimates (kg CH4ha−1 y−1) based on monthly measurements were: primary forest, 2.1; secondary forest, 1.0; active pasture, 1.3; degraded pasture, 3.1. The lower annual uptake in the active pasture compared with the primary forest was due to CH4 production during the wet season in the pasture soils, which is consistent with findings from other studies. In contrast, the degraded pasture was never a CH4 source. Expressing uptake as a negative flux and emission as a positive flux, CH4 fluxes were positively correlated with CO2 fluxes, indicating that root and microbial respiration in the productive pastures, and to a lesser extent in the primary forest, contributed to the formation of anaerobic microsites where CH4 was produced, whereas this productivity was absent in the degraded pasture. In all land uses, uptake rates of atmospheric CH4 were greater in the dry season than in the wet season, indicating the importance of soil water content and gas transport on CH4 fluxes. These clay soils had low annual uptake rates relative to reported rates on sandy soils, which also is consistent with gas transport within the soil being a limiting factor. Nitrogen availability indices did not correlate with CH4 fluxes, indicating that inhibition of CH4 oxidation was not an important mechanism explaining differences among land uses. At another ranch, Fazenda Agua Parada, no significant effect of pasture age was observed along a chronosequence of pasture ages. We conclude that land-use change can either increase or decrease the soil sink of CH4, depending on the duration of wet and dry seasons, the effects of seasonal precipitation on gas-phase transport, and the phenology and relative productivity of the vegetation in each land use.  相似文献   

5.
Sustainable management of grassland ecosystems for improved productivity can enhance their potential to sequester atmospheric CO2 in the soil. However, land-use management influences the quantity and quality of carbon (C) inputs which may, in turn, affect microbial activity and soil C decomposition rates. Understanding the potential changes in magnitude of soil C loss through respiration is critical for a comprehensive assessment of land-use conversion and grassland management impacts on terrestrial C dynamics. Thus, this study was designed to assess the effect of land-use management intensification on soil respiration in subtropical grasslands. Experimental sites consisted of a gradient of management intensities ranging from native rangeland (lowest), silvopasture (intermediate), to sown pasture (highest). Increasing management intensity from native rangeland to sown pasture elevated soil respiration. There was a significant effect of ‘season vs. management’ interaction on total soil respiration (RS), with greater increases in RS from summer to winter in sown pasture (∼200%) compared to native rangeland and silvopasture (∼91%). The temperature sensitivity of RS and heterotrophic soil respiration (RH) increased with management intensification, with a highest Q10 of 1.55 and 2.29, in sown pasture, compared to Q10 values of 1.09 and 1.48 in native rangelands. These results suggested that potential increases in soil C stock with intensification may be susceptible to faster turnover under warming climate scenarios. Improved resilience (and longer residence) of additionally sequestered soil C after intensification may be crucial for long-term ecological resilience, especially with changing climatic conditions. These findings are relevant for sustainable grassland management, especially within subtropical ecoregions, and add to the understanding of changes that may occur in rates of soil C losses as native grasslands are converted to more productive grassland ecosystems.  相似文献   

6.
In order to investigate the annual variation of soil respiration and its components in relation to seasonal changes in soil temperature and soil moisture in a Mediterranean mixed oak forest ecosystem, we set up a series of experimental treatments in May 1999 where litter (no litter), roots (no roots, by trenching) or both were excluded from plots of 4 m2. Subsequently, we measured soil respiration, soil temperature and soil moisture in each plot over a year after the forest was coppiced. The treatments did not significantly affect soil temperature or soil moisture measured over 0–10 cm depth. Soil respiration varied markedly during the year with high rates in spring and autumn and low rates in summer, coinciding with summer drought, and in winter, with the lowest temperatures. Very high respiration rates, however, were observed during the summer immediately after rainfall events. The mean annual rate of soil respiration was 2.9 µ mol m?2 s?1, ranging from 1.35 to 7.03 µmol m?2 s?1. Soil respiration was highly correlated with temperature during winter and during spring and autumn whenever volumetric soil water content was above 20%. Below this threshold value, there was no correlation between soil respiration and soil temperature, but soil moisture was a good predictor of soil respiration. A simple empirical model that predicted soil respiration during the year, using both soil temperature and soil moisture accounted for more than 91% of the observed annual variation in soil respiration. All the components of soil respiration followed a similar seasonal trend and were affected by summer drought. The Q10 value for soil respiration was 2.32, which is in agreement with other studies in forest ecosystems. However, we found a Q10 value for root respiration of 2.20, which is lower than recent values reported for forest sites. The fact that the seasonal variation in root growth with temperature in Mediterranean ecosystems differs from that in temperate regions may explain this difference. In temperate regions, increases in size of root populations during the growing season, coinciding with high temperatures, may yield higher apparent Q10 values than in Mediterranean regions where root growth is suppressed by summer drought. The decomposition of organic matter and belowground litter were the major components of soil respiration, accounting for almost 55% of the total soil respiration flux. This proportion is higher than has been reported for mature boreal and temperate forest and is probably the result of a short‐term C loss following recent logging at the site. The relationship proposed for soil respiration with soil temperature and soil moisture is useful for understanding and predicting potential changes in Mediterranean forest ecosystems in response to forest management and climate change.  相似文献   

7.
Soil respiration (R s) is an important component of the carbon cycle in terrestrial ecosystems, and changes in soil respiration with land cover alteration can have important implications for regional carbon balances. In southeastern China (Xiashu Experimental Forest, Jiangsu Province), we used an automated LI-8100 soil CO2 flux system to quantify diurnal variation of soil respiration in a secondary oak forest and a pine plantation. We found that soil respiration in the pine plantation was significantly higher than that in the secondary oak forest. There were similar patterns of soil respiration throughout the day in both the secondary oak forest and the pine plantation during our 7-month study (March–September 2005). The maximum of R s occurred between 4:00 pm and 7:00 pm. The diurnal variations of R s were usually out of phase with soil surface (0.5 cm) temperature (T g). However, annual variation in R s correlated with surface soil temperature. Soil respiration reached to a maximum in June, and decreased thereafter. The Q10 of R s in the secondary oak forest was significantly higher than that in the pine plantation. The higher Q10 value in the secondary oak forest implied that it might release more CO2 than the pine plantation under a global-warming scenario. Our results indicated that land-use change from secondary forest to plantation may cause a significant increase in CO2 emission, and reduce the temperature sensitivity of soil respiration in southeastern China.  相似文献   

8.
We measured the response of dark respiration (Rd) to temperature and foliage characteristics in the upper canopies of tree species in temperate rainforest communites in New Zealand along a soil chronosequence (six sites from 6 years to 120,000 years). The chronosequence provided a vegetation gradient characterised by significant changes in soil nutrition. This enabled us to examine the extent to which changes in dark respiration can be applied across forest biomes and the utility of scaling rules in whole-canopy carbon modelling. The response of respiration to temperature in the dominant tree species differed significantly between sites along the sequence. This involved changes in both Rd at a reference temperature (R10) and the extent to which Rd increased with temperature (described by Eo, a parameter related to the energy of activation, or the change in Rd over a 10°C range, Q10). Site averaged Eo ranged from 44.4 kJ mol–1 K–1 at the 60-year-old site to 26.0 kJ mol–1 K–1 at the oldest, most nutrient poor, site. Relationships between respiratory and foliage characteristics indicated that both the temperature response of respiration (Eo or Q10) and the instantaneous rate of respiration increased with both foliar nitrogen and phosphorus content. The ratio of photosynthetic capacity (Whitehead et al. in Oecologia 2005) to respiration (Amax/Rd) attained values in excess of 15 for species in the 6- to 120-year-old sites, but thereafter decreased significantly to around five at the 120,000-year-old site. This indicates that shoot carbon acquisition is regulated by nutrient limitations in the retrogressing ecosystems on the oldest sites. Our findings indicate that respiration and its temperature response will vary according to soil age and, therefore, to soil nutrient availability and the stage of forest development. Thus, variability in respiratory characteristics for canopies should be considered when using models to integrate respiration at large spatial scales.  相似文献   

9.
Variation in soil temperature can account for most of the seasonal and diel variation in soil CO2 efflux, but the temperature effect is not always consistent, and other factors such as soil water content are known to influence soil respiration. The objectives of this research were to study the spatial and temporal variation in soil respiration in a temperate forested landscape and to evaluate temperature and soil water functions as predictors of soil respiration. Soil CO2 fluxes were measured with chambers throughout an annual cycle in six study areas at the Harvard Forest in central Massachusetts that include soil drainage classes from well drained to very poorly drained. The mean annual estimate of soil CO2 efflux was 7.2 Mg ha–1, but ranged from 5.3 in the swamp site to 8.5 in a well-drained site, indicating that landscape heterogeneity is related to soil drainage class. An exponential function relating CO2 fluxes to soil temperature accounted for 80% of the seasonal variation in fluxes across all sites (Q10 = 3.9), but the Q10 ranged from 3.4 to 5.6 for the individual study sites. A significant drought in 1995 caused rapid declines in soil respiration rates in August and September in five of the six sites (a swamp site was the exception). This decline in CO2 fluxes correlated exponentially with decreasing soil matric potential, indicating a mechanistic effect of drought stress. At moderate to high water contents, however, soil water content was negatively correlated with soil temperature, which precluded distinguishing between the effects of these two confounded factors on CO2 flux. Occurrence of high Q10 values and variation in Q10 values among sites may be related to: (i) confounding effects of high soil water content; (ii) seasonal and diel patterns in root respiration and turnover of fine roots that are linked to above ground phenology and metabolism; and (iii) variation in the depth where CO2 is produced. The Q10 function can yield reasonably good predictions of annual fluxes of CO2, but it is a simplification that masks responses of root and microbial processes to variation in temperature and water content throughout the soil.  相似文献   

10.
Global warming and changes in rainfall amount and distribution may affect soil respiration as a major carbon flux between the biosphere and the atmosphere. The objectives of this study were to investigate the site to site and interannual variation in soil respiration of six temperate forest sites. Soil respiration was measured using closed chambers over 2 years under mature beech, spruce and pine stands at both Solling and Unterlüß, Germany, which have distinct climates and soils. Cumulative annual CO2 fluxes varied from 4.9 to 5.4 Mg C ha?1 yr?1 at Solling with silty soils and from 4.0 to 5.9 Mg C ha?1 yr?1 at Unterlüß with sandy soils. With one exception soil respiration rates were not significantly different among the six forest sites (site to site variation) and between the years within the same forest site (interannual variation). Only the respiration rate in the spruce stand at Unterlüß was significant lower than the beech stand at Unterlüß in both years. Soil respiration rates of the sandy sites at Unterlüß were limited by soil moisture during the rather dry and warm summer 1999 while soil respiration at the silty Solling site tended to increase. We found a threshold of ?80 kPa at 10 cm depth below which soil respiration decreased with increasing drought. Subsequent wetting of sandy soils revealed high CO2 effluxes in the stands at Unterlüß. However, dry periods were infrequent, and our results suggest that temporal variation in soil moisture generally had little effect on annual soil respiration rates. Soil temperature at 5 cm and 10 cm depth explained 83% of the temporal variation in soil respiration using the Arrhenius function. The correlations were weaker using temperature at 0 cm (r2 = 0.63) and 2.5 cm depth (r2 = 0.81). Mean Q10 values for the range from 5 to 15 °C increased asymptotically with soil depth from 1.87 at 0 cm to 3.46 at 10 cm depth, indicating a large uncertainty in the prediction of the temperature dependency of soil respiration. Comparing the fitted Arrhenius curves for same tree species from Solling and Unterlüß revealed higher soil respiration rates for the stands at Solling than in the respective stands at Unterlüß at the same temperature. A significant positive correlation across all sites between predicted soil respiration rates at 10 °C and total phosphorus content and C‐to‐N ratio of the upper mineral soil indicate a possible effect of nutrients on soil respiration.  相似文献   

11.
Soil temperature and moisture influence soil respiration at a range of temporal and spatial scales. Although soil temperature and moisture may be seasonally correlated, intra and inter-annual variations in soil moisture do occur. There are few direct observations of the influence of local variation in species composition or other stand/site characteristics on seasonal and annual variations in soil moisture, and on cumulative annual soil carbon release. Soil climate and soil respiration from twelve sites in five different forest types were monitored over a 2-year period (1998–1999). Also measured were stand age, species composition, basal area, litter inputs, total above-ground wood production, leaf area index, forest floor mass, coarse and fine root mass, forest floor carbon and nitrogen concentration, root carbon and nitrogen concentration, soil carbon and nitrogen concentration, coarse fraction mass and volume, and soil texture. General soil respiration models were developed using soil temperature, daily soil moisture, and various site/soil characteristics. Of the site/soil characteristics, above-ground production, soil texture, roots + forest floor mass, roots + forest floor carbon:nitrogen, and soil carbon:nitrogen were significant predictors of soil respiration when used alone in respiration models; all of these site variables were weakly to moderately correlated with mean site soil moisture. Daily soil climate data were used to estimate the annual release of carbon (C) from soil respiration for the period 1998–1999. Mean annual soil temperature did not differ between the 2 years but mean annual soil moisture was approximately 9% lower in 1998 due to a summer drought. Soil C respired during 1998 ranged from 8.57 to 11.43 Mg C ha−1 yr−1 while the same sites released 10.13 and 13.57 Mg C ha−1 yr−1 in 1999; inter-annual differences of 15.41 and 15.73%, respectively. Among the 12 sites studied, we calculated that the depression of soil respiration linked to the drought caused annual differences of soil respiration from 11.00 to 15.78%. Annual estimates of respired soil C decreased with increasing site mean soil moisture. Similarly, the difference of respired carbon between the drought and the non-drought years generally decreased with increasing site mean soil moisture.  相似文献   

12.
Over two-thirds of terrestrial carbon is stored belowground and a significant amount of atmospheric CO2 is respired by roots and microbes in soils. For this analysis, soil respiration (Rs) data were assembled from 31 AmeriFlux and CarboEurope sites representing deciduous broadleaf, evergreen needleleaf, grasslands, mixed deciduous/evergreen and woodland/savanna ecosystem types. Lowest to highest rates of soil respiration averaged over the growing season were grassland and woodland/savanna < deciduous broadleaf forests < evergreen needleleaf, mixed deciduous/evergreen forests with growing season soil respiration significantly different between forested and non-forested biomes (p < 0.001). Timing of peak respiration rates during the growing season varied from March/April in grasslands to July–September for all other biomes. Biomes with overall strongest relationship between soil respiration and soil temperature were from the deciduous and mixed forests (R2 ≥ 0.65). Maximum soil respiration was weakly related to maximum fine root biomass (R2 = 0.28) and positively related to the previous years’ annual litterfall (R2 = 0.46). Published rates of annual soil respiration were linearly related to LAI and fine root carbon (R2 = 0.48, 0.47), as well as net primary production (NPP) (R2 = 0.44). At 10 sites, maximum growing season Rs was weakly correlated with annual GPP estimated from eddy covariance towersites (R2 = 0.29; p < 0.05), and annual soil respiration and total growing season Rs were not correlated with annual GPP (p > 0.1). Yet, previous studies indicate correlations on shorter time scales within site (e.g., weekly, monthly). Estimates of annual GPP from the Biome-BGC model were strongly correlated with observed annual estimates of soil respiration for six sites (R2 = 0.84; p < 0.01). Correlations from observations of Rs with NPP, LAI, fine root biomass and litterfall relate above and belowground inputs to labile pools that are available for decomposition. Our results suggest that simple empirical relationships with temperature and/or moisture that may be robust at individual sites may not be adequate to characterize soil CO2 effluxes across space and time, agreeing with other multi-site studies. Information is needed on the timing and phenological controls of substrate availability (e.g., fine roots, LAI) and inputs (e.g., root turnover, litterfall) to improve our ability to accurately quantify the relationships between soil CO2 effluxes and carbon substrate storage.For this study, these authors received significant contributions from: M. Aubinet, D. Baldocchi, C. Bernhofer, P. Bolstad, A. Bosc, J.L. Campbell, Y. Cheng, J. Curiel Yuste, P. Curtis, E.A. Davidson, D. Epron, A. Granier, T. Grünwald, D. Hollinger, I.A. Janssens, B. Longdoz, D. Loustau, J. Martin, R. Monson, W. Oechel, J. Pippen, F. Ponti, R. Ryel, K. Savage, L. Scott-Denton, J.-A. Subke, J. Tang, J. Tenhunen, V. Turcu, C. S. Vogel.  相似文献   

13.
Over the past decades, the tropical mountain rainforest of southern Ecuador has been threatened by conversion to cattle pastures. Frequently, these pastures are invaded by bracken fern and abandoned when bracken becomes dominant. Changes in land-use (forest–pasture–abandoned pasture) can affect soil microorganisms and their physiological responses with respect to soil carbon and nutrient cycling. In situ investigations on litter decomposition and soil respiration as well as biogeochemical characterization of the soil were carried out to identify the driving factors behind. The conversion of forest to pasture induced a pronounced increase in CO2–C effluxes to 12.2 Mg ha?1 a?1 which did not decrease after abandonment. Soil microbial activity and biomass showed a different pattern with lowest values at forest and abandoned pasture sites. With 3445 mg kg?1 (0–5 cm) microbial biomass carbon (MBC by CFE-method), the active pasture had a more than three times higher value than forest and abandoned pasture, which was among the highest in tropical pasture soils. A shift in the microbial community structure (phospholipid fatty acid, PLFA) was also induced by the establishment of pasture land; the relative abundance of fungi and Gram-negative bacteria increased. PLFA fingerprints of the forest organic layer were more similar to pasture than to forest mineral soil. Chemical properties (pH value, exchangeable cations) were the main factors influencing the respective microbial structure. Bracken-invasion resulted in a decrease in the quantity and quality of above- and belowground biomass. The lower organic substance and nutrient availability induced a significant decline in microbial biomass and activity. After pasture abandonment, these differences in soil microbial function were not accompanied by pronounced shifts in the community structure and in soil pH as was shown for the conversion to pasture. A disconnection between microbial structure and function was identified. Similar soil CO2–C effluxes between active and abandoned pasture sites might be explained by an underestimation of the effluxes from the active pasture site. All measurements were carried out between grass tussocks where fine-root density was about 2.6 times lower than below tussocks. Thus, lower proportions of root respiration were expected than below tussocks. Overall, soil microorganisms responded differently to changes in land-use from forest to pasture and from pasture to abandoned pasture resulting in pronounced changes of carbon and nutrient cycling and hence of ecosystem functioning.  相似文献   

14.
To better understand the effects of local topography and climate on soil respiration, we conducted field measurements and soil incubation experiments to investigate various factors influencing spatial and temporal variations in soil respiration for six mixed‐hardwood forest slopes in the midst of the Korean Peninsula. Soil respiration and soil water content (SWC) were significantly greater (P=0.09 and 0.003, respectively) on north‐facing slopes compared to south‐facing slopes, while soil temperature was not significantly different between slopes (P>0.5). At all sites, soil temperature was the primary factor driving temporal variations in soil respiration (r2=0.84–0.96) followed by SWC, which accounted for 30% of soil respiration spatial and temporal variability. Results from both field measurements and incubation experiments indicate that variations in soil respiration due to aspect can be explained by a convex‐shaped function relating SWC to normalized soil respiration rates. Annual soil respiration estimates (1070–1246 g C m?2 yr?1) were not closely related to mean annual air temperatures among sites from different climate regimes. When soils from each site were incubated at similar temperatures in a laboratory, respiration rates for mineral soils from wetter and cooler sites were significantly higher than those for the drier and warmer sites (n=4, P<0.01). Our results indicate that the application of standard temperature‐based Q10 models to estimate soil respiration rates for larger geographic areas covering different aspects or climatic regimes are not adequate unless other factors, such as SWC and total soil nitrogen, are considered in addition to soil temperature.  相似文献   

15.
Responses of soil respiration (CO2 emission) to simulated N deposition were studied in a disturbed (reforested forest with previous understory and litter harvesting) and a rehabilitated (reforested forest with no understory and litter harvesting) tropical forest in southern China from October 2005 to September 2006. The objectives of the study were to test the following hypotheses: (1) soil respiration is higher in rehabilitated forest than in disturbed forest; (2) soil respiration in both rehabilitated and disturbed tropical forests is stimulated by N additions; and (3) soil respiration is more sensitive to N addition in disturbed forest than in rehabilitated forest due to relatively low soil nutrient status in the former, resulting from different previous human disturbance. Static chamber and gas chromatography techniques were employed to quantify the soil respiration, following different N treatments (Control, no N addition; Low-N, 5 g N m−2 year−1; Medium-N, 10 g N m−2 year−1), which had been applied continuously for 26 months before the respiration measurement. Results showed that soil respiration exhibited a strong seasonal pattern, with the highest rates observed in the hot and wet growing season (April–September) and the lowest rates in winter (December–February) in both rehabilitated and disturbed forests. Soil respiration rates exhibited significant positive exponential relationship with soil temperature and significant positive linear relationship with soil moisture. Soil respiration was also significantly higher in the rehabilitated forest than in the disturbed forest. Annual mean soil respiration rate in the rehabilitated forest was 20% lower in low-N plots (71 ± 4 mg CO2-C m−2 h−1) and 10% lower in medium-N plots (80 ± 4 mg CO2-C m−2 h−1) than in the control plots (89 ± 5 mg CO2-C m−2 h−1), and the differences between the control and low-N or medium-N treatments were statistically significant. In disturbed forest, annual mean soil respiration rate was 5% lower in low-N plots (63 ± 3 mg CO2-C m−2 h−1) and 8% lower in medium-N plots (61 ± 3 mg CO2-C m−2 h−1) than in the control plots (66 ± 4 mg CO2-C m−2 h−1), but the differences among treatments were not significant. The depressed effects of experimental N deposition occurred mostly in the hot and wet growing season. Our results suggest that response of soil respiration to elevated N deposition in the reforested tropical forests may vary depending on the status of human disturbance. Responsible Editor: Hans Lambers.  相似文献   

16.
Microbiological and physico-chemical characteristics of tropical forest, grassland and cropfield soils from India were investigated. The study revealed that the conversion of natural forest led to a reduction of soil organic C (26–36%), total N (26–35%), total P (33–44%), microfungal biomass (44–66%) and total microbial biomass C, N and P (25–60%) over a period of 30–50 years. Comparative analysis of microbial activity in terms of basal soil respiration revealed maximum activity in the forest and minimum in the cropfield soil. Analysis of microbial metabolic respiratory activity (qCO2) indicated relatively greater respiratory loss of CO2-C per unit microbial biomass in cropfield and grassland than in forest soil. Considering the importance of the microbial component in soil, we conclude that the conversion of the tropical forest to different land uses leads to the loss of biological stability of the soil.  相似文献   

17.
Soil respiration and the hydrolysis of fluorescein diacetate (FDA) as a measure of total microbial activity were investigated in central Korea, at three sites that had been changed from abandoned agricultural lands to natural vegetation: rice field conversion to forest (RF), crop field conversion to shrub (CS), and indigenous forest (IF). Seasonal variations in soil respiration were affected by soil temperature and, to a lesser extent, by photosynthetically active radiation (PAR) and soil moisture. The mean annual rate of soil respiration (g CO2 m-2 hr-1) was highest at CS (0.36), followed by IF (0.29) and RF (0.28), whereas the total annual soil respiration (kg CO2 m-2 yr-1) was 2.82 for CS, 2.46 for IF, and 2.40 for RF. Mean annual FDA hydrolysis (μg FDA min-1 g-1 dry soil) was higher at RS (4.56) and IF (4.61) than at CS (3.65). At all three land-use change sites, soil respiration was only very weakly correlated with FDA hydrolysis.  相似文献   

18.
Soil microbial respiration is a critical component of the global carbon cycle, but it is uncertain how properties of microbes affect this process. Previous studies have noted a thermodynamic trade-off between the rate and efficiency of growth in heterotrophic organisms. Growth rate and yield determine the biomass-specific respiration rate of growing microbial populations, but these traits have not previously been used to scale from microbial communities to ecosystems. Here we report seasonal variation in microbial growth kinetics and temperature responses (Q10) in a coniferous forest soil, relate these properties to cultured and uncultured soil microbes, and model the effects of shifting growth kinetics on soil heterotrophic respiration (Rh). Soil microbial communities from under-snow had higher growth rates and lower growth yields than the summer and fall communities from exposed soils, causing higher biomass-specific respiration rates. Growth rate and yield were strongly negatively correlated. Based on experiments using specific growth inhibitors, bacteria had higher growth rates and lower yields than fungi, overall, suggesting a more important role for bacteria in determining Rh. The dominant bacteria from laboratory-incubated soil differed seasonally: faster-growing, cold-adapted Janthinobacterium species dominated in winter and slower-growing, mesophilic Burkholderia and Variovorax species dominated in summer. Modeled Rh was sensitive to microbial kinetics and Q10: a sixfold lower annual Rh resulted from using kinetic parameters from summer versus winter communities. Under the most realistic scenario using seasonally changing communities, the model estimated Rh at 22.67 mol m−2 year−1, or 47.0% of annual total ecosystem respiration (Re) for this forest.  相似文献   

19.
Sparse Ulmus pumila woodlands play an important role in contributing to ecosystem function in semi-arid grassland of northern China. To understand the key attributes of soil carbon cycling in U. pumila woodland, we studied dynamics of soil respiration in the canopy field (i.e., the projected crown cover area) and the open field at locations differing in distance (i.e., at 1–1.5, 3–4, 10, and >15 m) to tree stems from July through September of 2005, and measured soil biotic factors (e.g., fine root mass, soil microbial biomass, and activity) and abiotic factors [e.g., soil water content (SWC) and organic carbon] in mid-August. Soil respiration was further separated into root component and microbial component at the end of the field measurement in September. Results showed that soil respiration had a significant exponent relationship with soil temperature at 10-cm depth. The temperature sensitivity index of soil respiration, Q 10, was lower than the global average of 2.0, and declined significantly (P < 0.05) with distance. The rate of soil respiration was generally greater in the canopy field than in the open field; monthly mean of soil respiration was 305.5–730.8 mg CO2 m−2 h−1 in the canopy field and 299.6–443.1 mg CO2 m−2 h−1 in the open field from July through September; basal soil respiration at 10°C declined with distance, and varied from ~250 mg CO2 m−2 h−1 near tree stems to <200 mg CO2 m−2 h−1 in the open field. Variations in soil respiration with distance were consistent with patterns of SWC, fine root mass, microbial biomass and activities. Regression analysis indicated that soil respiration was tightly coupled with microbial respiration and only weakly related to root respiration. Overall, variations in SWC, soil nutrients, microbial biomass, and microbial activity are largely responsible for the spatial heterogeneity of soil respiration in this semi-arid U. pumila woodland.  相似文献   

20.
A simulation study based on recent regional climate scenarios for Sweden investigated possible changes in carbon (C) dynamics and net ecosystem exchange (NEE) of Swedish Norway spruce forest ecosystems. Four sites, representative of well-drained soils in four regions, were included. Stand development was simulated for a 100-year rotation period using a coupled model describing abiotic and biotic processes in the soil-plant-atmosphere system. Two IPCC climate change scenarios, corresponding to a mean annual temperature increase of about 2°C (A2) or 3°C (B2) from the reference period 1961–1990 to a new period 2061–2090, were considered. Annual maximum snow depth decreased with the increase in air temperature, whereas maximum soil frost depth and mean annual soil temperature showed only small changes, especially for the sites in northern Sweden. Simulations suggested that in the warmer climate, gross primary production (GPP) increased by 24–32% in northern Sweden and by 32–43% in the south. In the north, the increase was related to the combined effect of air and soil temperature extending the growing season, whereas in the south it was mainly governed by increased N availability due to increased soil temperature. NEE increased by about 20% (A2) or 25% (B2) at all sites, more or less solely due to increased accumulation of C in the tree biomass (including harvest residues), since changes in soil C were small compared with the current climate. Both light use efficiency and water use efficiency were improved in the future climate scenarios, despite increases in atmospheric CO2 not being considered.  相似文献   

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