Plant carbon inputs and environmental factors strongly affect soil respiration in a subtropical forest of southwestern China

Soil respiration is a large component of global carbon fluxes, so it is important to explore how this carbon flux varies with environmental factors and carbon inputs from plants. As part of a long-term study on the chemical and biological effects of aboveground litterfall denial, root trenching and tree-stem girdling, we measured soil respiration for three years in plots where those treatments were applied singly and in combination. Tree-stem girdling terminates the flow of carbohydrates from canopy, but allows the roots to continue water and nutrient uptake. After carbon storage below the stem girdles is depleted, the girdled trees die. Root trenching immediately terminates root exudates as well as water and nutrient uptake. Excluding aboveground litterfall removes soil carbon inputs, but allows normal root functions to continue. We found that removing aboveground litterfall and the humus layer reduced soil respiration by more than the C input from litter, a respiration priming effect. When this treatment was combined with stem girdling, root trenching or those treatments in combination, the change in soil respiration was indistinguishable from the loss of litterfall C inputs. This suggests that litterfall priming occurs only when normal root processes persist. Soil respiration was significantly related to temperature in all treatment combinations, and to soil water content in all treatments except stem girdling alone, and girdling plus trenching. Aboveground litterfall was a significant predictor of soil respiration in control, stem-girdled, trenched and stem-girdled plus trenching treatments. Stem girdling significantly reduced soil respiration as a single factor, but root trenching did not. These results suggest that in addition to temperature, aboveground carbon inputs exert strong controls on forest soil respiration.     

Subtropical plantations are large carbon sinks: Evidence from two monoculture plantations in South China

Quantifying the net carbon (C) storage of forest plantations is required to assess their potential to offset fossil fuel emissions. In this study, a biometric approach was used to estimate net ecosystem productivity (NEP) for two monoculture plantations in South China: Acacia crassicarpa and Eucalyptus urophylla. This approach was based on stand-level net primary productivity (NPP, based on direct biometric inventory) and heterotrophic respiration (R_h). In comparisons of R_h determination based on trenching vs. tree girdling, both trenching and tree girdling changed soil temperature and soil moisture relative to undisturbed control plots, and we assess the effects of corrections for disturbances of soil moisture and soil moisture on the estimation of soil CO₂ efflux partitioning. Soil microbial biomass and dissolved organic carbon were significantly lower in trenched plots than in tree girdled plots for both plantations. Annual soil CO₂ flux in trenched plots (R_h-t) was significantly lower than in tree-girdled plots (R_h-g) in both plantations. The estimates of R_h-t and R_h-g, expressed as a percentage of total soil respiration, were 58 ± 4% and 74 ± 6%, respectively, for A. crassicarpa, and 64 ± 3% and 78 ± 5%, respectively, for E. urophylla. By the end of experiment, the difference in soil CO₂ efflux between the trenched plots and tree-girdled plots had become small for both plantations. Annual R_h (mean of the annual R_h-t and R_h-g) and net primary production (NPP) were 470 ± 25 and 800 ± 118 g C m⁻² yr⁻¹, respectively, for A. crassicarpa, and 420 ± 35 and 2380 ± 187 g C m⁻² yr⁻², respectively, for E. urophylla. The two plantations in the developmental stage were large carbon sinks: NEP was 330 ± 76 C m⁻² yr⁻¹ for A. crassicarpa and 1960 ± 178 g C m⁻² yr⁻¹ for E. urophylla.     

Estimating heterotrophic and autotrophic soil respiration using small-area trenched plot technique: Theory and practice

The trenching method of root exclusion is generally used to estimate heterotrophic (microbial decomposition) (F_h) and autotrophic (root and associated rhizosphere respiration) (F_a) components of soil respiration (F₀), particularly in forest ecosystems. However, some uncertainties exist on the accuracy and interpretation of the results from such experiments using small-area root exclusion plots. Using field and laboratory measurements as well as simulations using a process-based model of CO₂ production and transport in soil, we show that: (a) CO₂ concentrations at or immediately below the depth of root exclusion in small-area root exclusion plots are similar to those at the same depth in nearby undisturbed soil and (b) the contribution of soil CO₂ flux from below the root exclusion depth to the measured efflux at the surface of a root exclusion plot (F_0re) is increased because of the higher concentration gradient at the bottom of the root exclusion layer due to the decreased rate of CO₂ production above this depth. Consequently, F_a, calculated as F_0c measured in control (non-disturbed) plots minus F_0re measured in root exclusion plots, is underestimated. We describe an analytical model, derived from the soil CO₂ production and diffusion equation, to obtain correct estimates of F_a measured using small-area root exclusion plots. The analytical model requires knowledge of depth distribution of soil CO₂ diffusivity and source strength as inputs.     

Effects of trenching on soil processes and properties in a New Mexico mixed-conifer forest

Summary Trenching was used to reduce root activity in treeless plots in a New Mexico mixed-conifer forest to examine the effects of plant roots on soil processes. Trenching led to increases in moisture content (104%), inorganic N concentration (115%), and mass loss from cellulose (196%). In laboratory incubations, trenched soils collected in the 1st and 2nd year after trenching evolved 52% and 115% more CO₂, respectively, than control soils. Amending incubated trenched and control soils with moisture and inorganic N indicated that increased soil moisture content in trenched plots could explain the increased microbial activity. Trenching also had statistically significant but inconsistent effects on net N mineralization in incubated soils. The greatest effect of trenching was to increase net N mineralization under favorable temperature and moisture conditions. Irrigation of field plots increased both CO₂ evolution and net N mineralization. Overall, these data are consistent with the hypothesis that plant roots reduced microbial activity by moisture uptake during the time of the study.     

A comparison of trenched plot techniques for partitioning soil respiration

Partitioning the soil surface CO₂ flux (R_S) flux is an important step in understanding ecosystem-level carbon cycling, given that R_S is poorly constrained and its source components may have different sensitivities to climate change. Trenched plots are an inexpensive but labor-intensive method of separating the R_S flux into its root (autotrophic) and soil (heterotrophic) components. This study tested if various methods of plant suppression in trenched plots affected R_S fluxes, quantified the R_S response to soil temperature and moisture changes, and estimated the heterotrophic contribution to R_S. It was performed in a boreal black spruce (Picea mariana) plantation, using a randomized complete block design, during the 2007 and 2008 growing seasons. Trenched plots had significantly lower R_S than control plots, with differences appearing ∼100 days after trenching; spatial variability doubled immediately after trenching but then declined throughout the experiment. Most trenching treatments had significantly lower (by ∼0.5 μmol CO₂ m⁻² s⁻¹) R_S than the controls, and there was no significant difference in R_S among the various trenching treatments. Soil temperature at 2 cm explained more R_S variability than did 10-cm temperature or soil moisture. Temperature sensitivity (Q₁₀) declined in the control plots from ∼2.6 (at 5 °C) to ∼1.6 (at 15 °C); trenched plots values were higher, from 3.1 at 5 °C to 1.9 at 15 °C. We estimated R_S for the study period to be 241 ± 40 g C m⁻², with live roots contributing 64% of R_S after accounting for fine root decay, and 293 g C m⁻² for the entire year. These findings suggest that laborious hand weeding of trenched plot vegetation may be replaced by other methods, facilitating future studies of this large and poorly-understood carbon flux.     

Litter decomposition in beech forests — effects of excluding tree roots

Summary The hypothesis proposed by Gadgil and Gadgil (1971) that mycorrhizal tree roots suppress the decomposition of forest litter was examined in trenching experiments. The tests were conducted in two beech forest sites in southern Sweden, one with mor and one with mull. The exclusion of tree roots had no apparent influence on litter mass loss at any of the sites, which differed markedly in soil fertility and root distribution. Nor did trenching have any significant effect on total organic matter over the following 6 years, although trenched plots tended to be wetter than undisturbed soil. The present results as well as results from other similar studies suggest that the suppression of litter turnover by mycorrhizal tree roots is not an important mechanism in northern temperate and boreal forests.     

Effects of root and litter exclusion on soil CO2 efflux and microbial biomass in wet tropical forests

We examined the effects of root and litter exclusion on the rate of soil CO₂ efflux and microbial biomass at a soil depth of 25 cm in a secondary forest (dominated by Tabebuia heterophylla) and a pine (Pinus caribaea) plantation in the Luquillo Experimental Forest in Puerto Rico. The experimental plots were initially established in 1990, when root, forest floor mass and new litterfall were excluded for 7 y since then. Soil respiration was significantly reduced in the litter and root exclusion plots in both the secondary forest and the pine plantation compared with the control. Root exclusion had a greater effect on soil CO₂ efflux than the litter exclusion in the plantation, whereas a reversed pattern was observed in the secondary forest. The reduction of microbial biomass in the root exclusion plot was greater in the secondary forest (59%) than in the plantation (31%), while there was no difference of the reduction in the litter exclusion plots between these forests. Our results suggest that above-ground input and roots (root litter and exudates) differentially affect soil CO₂ efflux under different vegetation types.     

Above- and belowground carbon inputs affect seasonal variations of soil microbial biomass in a subtropical monsoon forest of southwest China

Soil microbial activity drives carbon and nutrient cycling in terrestrial ecosystems. Soil microbial biomass is commonly limited by environmental factors and soil carbon availability. We employed plant litter removal, root trenching and stem-girdling treatments to examine the effects of environmental factors, above- and belowground carbon inputs on soil microbial C in a subtropical monsoon forest in southwest China. During the experimental period from July 2006 through April 2007, 2 years after initiation of the treatments, microbial biomass C in the humus layer did not vary with seasonal changes in soil temperature or water content. Mineral soil microbial C decreased throughout the experimental period and varied with soil temperature and water content. Litter removal reduced mineral soil microbial C by 19.0% in the ungirdled plots, but only 4.0% in girdled plots. Root trenching, stem girdling and their interactions influenced microbial C in humus layer. Neither root trenching nor girdling significantly influenced mineral soil microbial C. Mineral soil microbial C correlated with following-month plant litterfall in control plots, but these correlations were not observed in root-trenching plots or girdling plots. Our results suggest that belowground carbon retranslocated from shoots and present in soil organic matter, rather than aboveground fresh plant litter inputs, determines seasonal fluctuation of mineral soil microbial biomass.     

Photodegradation effects on CO2 emissions from litter and SOM and photo-facilitation of microbial decomposition in a California grassland

Decomposition of soil organic matter (SOM) and plant litter has been shown to be affected by high solar radiation; this could partly explain why biogeochemical models underestimate decomposition in arid and semi-arid ecosystems. We set out to test the effect of using traditional PVC chambers for measuring soil gas fluxes versus quartz chambers that allowed passage of light during field measurements in a dry-land field in Davis, CA. Results showed that fluxes from quartz-top chambers were on average 29% higher than from opaque chambers. We also studied the effect of solar light exposure on decomposition of native grass litter and SOM in a field experiment where plots were shaded or left exposed for 157 days during summer; litter did not seem to be affected by exposure to light. However, we concluded that SOM decomposition was affected by light exposure since shaded soil had similar respiration to sunlight-exposed soil indicating that microbial respiration occurred under the shade while photo-degradation likely occurred under the sun. Additionally, ¹⁵N-labeled grass was placed in litter bags in the field with either clear filters to allow light or aluminum covers to block light; 3-month exposure caused a change in lignin degradability as indicated by the change in the Ad/Al ratio. Incubation of that litter showed 9.3% more CO₂ produced from litter in clear and aluminum bags than unexposed litter. This showed that photo-facilitation occurred although to a small degree and was a result of light exposure and/or heat degradation. We attributed the similar respiration from clear- and aluminum-exposed litter to heat degradation of the aluminum-exposed litter. In conclusion, our results show that in hot dry ecosystems conventional PVC chambers underestimate measured CO₂ flux rates; sunlight exposure changes litter chemistry and appears to affect the degradation of soil organic matter, but the magnitude of degradation depends on an interaction of factors such as soil temperature and moisture.     

Variation of soil respiration at three spatial scales: Components within measurements, intra-site variation and patterns on the landscape

Soil respiration is an important component of terrestrial carbon cycling and can be influenced by many factors that vary spatially. This research aims to determine the extent and causes of spatial variation of soil respiration, and to quantify the importance of scale on measuring and modeling soil respiration within and among common forests of Northern Wisconsin. The potential sources of variation were examined at three scales: [1] variation among the litter, root, and bulk soil respiration components within individual 0.1 m measurement collars, [2] variation between individual soil respiration measurements within a site (<1 m to 10 m), and [3] variation on the landscape caused by topographic influence (100 m to 1000 m). Soil respiration was measured over a two-year period at 12 plots that included four forest types. Root exclusion collars were installed at a subset of the sites, and periodic removal of the litter layer allowed litter and bulk soil contributions to be estimated by subtraction. Soil respiration was also measured at fixed locations in six northern hardwood sites and two aspen sites to examine the stability of variation between individual measurements. These study sites were added to an existing data set where soil respiration was measured in a random, rotating, systematic clustering which allowed the examination of spatial variability from scales of <1 m to 100+ m. The combined data set for this area was also used to examine the influence of topography on soil respiration at scales of over 1000 m by using a temperature and moisture driven soil respiration model and a 4 km² digital elevation model (DEM) to model soil moisture. Results indicate that, although variation of soil respiration and soil moisture is greatest at scales of 100 m or more, variation from locations 1 m or less can be large (standard deviation during summer period of 1.58 and 1.28 μmol CO₂ m⁻² s⁻¹, respectively). At the smallest of scales, the individual contributions of the bulk soil, the roots, and the litter mat changed greatly throughout the season and between forest types, although the data were highly variable within any given site. For scales of 1-10 m, variation between individual measurements could be explained by positive relationships between forest floor mass, root mass, carbon and nitrogen pools, or root nitrogen concentration. Lastly, topography strongly influenced soil moisture and soil properties, and created spatial patterns of soil respiration which changed greatly during a drought event. Integrating soil fluxes over a 4 km² region using an elevation dependent soil respiration model resulted in a drought induced reduction of peak summer flux rates by 37.5%, versus a 31.3% when only plot level data was used. The trends at these important scales may help explain some inter-annual and spatial variability of the net ecosystem exchange of carbon.     

Winter soil CO2 efflux and its contribution to annual soil respiration in different ecosystems of a forest-steppe ecotone, north China

Most soil respiration measurements are conducted during the growing season. In tundra and boreal forest ecosystems, cumulative winter soil CO₂ fluxes are reported to be a significant component of their annual carbon budgets. However, little information on winter soil CO₂ efflux is known from mid-latitude ecosystems. Therefore, comparing measurements of soil respiration taken annually versus during the growing season will improve the accuracy of ecosystem carbon budgets and the response of soil CO₂ efflux to climate changes. In this study we measured winter soil CO₂ efflux and its contribution to annual soil respiration for seven ecosystems (three forests: Pinus sylvestris var. mongolica plantation, Larix principis-rupprechtii plantation and Betula platyphylla forest; two shrubs: Rosa bella and Malus baccata; and two meadow grasslands) in a forest-steppe ecotone, north China. Overall mean winter and growing season soil CO₂ effluxes were 0.15-0.26 μmol m⁻² s⁻¹ and 2.65-4.61 μmol m⁻² s⁻¹, respectively, with significant differences in the growing season among the different ecosystems. Annual Q₁₀ (increased soil respiration rate per 10 °C increase in temperature) was generally higher than the growing season Q₁₀. Soil water content accounted for 84% of the variations in growing season Q₁₀ and soil temperature range explained 88% of the variation in annual Q₁₀. Soil organic carbon density to 30 cm depth was a good surrogate for SR₁₀ (basal soil respiration at a reference temperature of 10 °C). Annual soil CO₂ efflux ranged from 394.76 g C m⁻² to 973.18 g C m⁻² using observed ecosystem-specific response equations between soil respiration and soil temperature. Estimates ranged from 424.90 g C m⁻² to 784.73 g C m⁻² by interpolating measured soil respiration between sampling dates for every day of the year and then computing the sum to obtain the annual value. The contributions of winter soil CO₂ efflux to annual soil respiration were 3.48-7.30% and 4.92-7.83% using interpolated and modeled methods, respectively. Our results indicate that in mid-latitude ecosystems, soil CO₂ efflux continues throughout the winter and winter soil respiration is an important component of annual CO₂ efflux.     

凋落物对土壤呼吸的贡献研究进展

土壤呼吸是土壤碳库输出的主要途径,凋落物是影响土壤呼吸的重要因素。明确凋落物对土壤呼吸的贡献,有助于准确评估植物-土壤-大气三个碳库之间的碳收支过程。本文综述了近年来国内外有关凋落物对土壤呼吸贡献的研究成果,阐明了凋落物对土壤呼吸的贡献机理,讨论了凋落物对土壤呼吸贡献率及其存在的时空分异特征,在此基础上,对该领域研究前景进行了展望。     

Alterations in forest detritus inputs influence soil carbon concentration and soil respiration in a Central-European deciduous forest

In a Quercetum petraeae–cerris forest in northeastern Hungary, we examined effects of litter input alterations on the quantity and quality soil carbon stocks and soil CO₂ emissions. Treatments at the Síkfőkút DIRT (Detritus Input and Removal Treatments) experimental site include adding (by doubling) of either leaf litter (DL) or wood (DW) (including branches, twigs, bark), and removing all aboveground litter (NL), all root inputs by trenching (NR), or removing all litter inputs (NI). Within 4 years we saw a significant decrease in soil carbon (C) concentrations in the upper 15 cm for root exclusion plots. Decreases in C for the litter exclusion treatments appeared later, and were smaller than declines in root exclusion plots, highlighting the role of root detritus in the formation of soil organic matter in this forest. By year 8 of the experiment, surface soil C concentrations were lower than Control plots by 32% in NI, 23% in NR and 19% in NL. Increases in soil C in litter addition treatments were less than C losses from litter exclusion treatments, with surface C increasing by 12% in DL and 6% in DW. Detritus additions and removals had significant effects on soil microclimate, with decreases in seasonal variations in soil temperature (between summer and winter) in Double Litter plots but enhanced seasonal variation in detritus exclusion plots. Carbon dioxide (CO₂) emissions were most influenced by detritus input quantity and soil organic matter concentration when soils were warm and moist. Clearly changes in detritus inputs from altered forest productivity, as well as altered litter impacts on soil microclimate, must be included in models of soil carbon fluxes and pools with expected future changes in climate.     

Controls on soil respiration in semiarid soils

Soil respiration in semiarid ecosystems responds positively to temperature, but temperature is just one of many factors controlling soil respiration. Soil moisture can have an overriding influence, particularly during the dry/warm portions of the year. The purpose of this project was to evaluate the influence of soil moisture on the relationship between temperature and soil respiration. Soil samples collected from a range of sites arrayed across a climatic gradient were incubated under varying temperature and moisture conditions. Additionally, we evaluated the impact of substrate quality on short-term soil respiration responses by carrying out substrate-induced respiration assessments for each soil at nine different temperatures. Within all soil moisture regimes, respiration rates always increased with increase in temperature. For a given temperature, soil respiration increased by half (on average) across moisture regimes; Q₁₀ values declined with soil moisture from 3.2 (at −0.03 MPa) to 2.1 (−1.5 MPa). In summary, soil respiration was generally directly related to temperature, but responses were ameliorated with decrease in soil moisture.     

Carbon dioxide emissions of soils under pure and mixed stands of beech and spruce, affected by decomposing foliage litter mixtures

Soil respiration is the largest terrestrial source of CO₂ to the atmosphere. In forests, roughly half of the soil respiration is autotrophic (mainly root respiration) while the remainder is heterotrophic, originating from decomposition of soil organic matter. Decomposition is an important process for cycling of nutrients in forest ecosystems. Hence, tree species induced changes may have a great impact on atmospheric CO₂ concentrations. Since studies on the combined effects of beech-spruce mixtures are very rare, we firstly measured CO₂ emission rates in three adjacent stands of pure spruce (Picea abies), mixed spruce-beech and pure beech (Fagus sylvatica) on three base-rich sites (Flysch) and three base-poor sites (Molasse; yielding a total of 18 stands) during two summer periods using the closed chamber method. CO₂ emissions were higher on the well-aerated sandy soils on Molasse than on the clayey soils on Flysch, characterized by frequent water logging. Mean CO₂ effluxes increased from spruce (41) over the mixed (55) to the beech (59) stands on Molasse, while tree species effects were lower on Flysch (30-35, mixed > beech = spruce; all data in mg CO₂-C m⁻² h⁻¹). Secondly, we studied decomposition after fourfold litter manipulations at the 6 mixed species stands: the O_i - and O_e horizons were removed and replaced by additions of beech -, spruce - and mixed litter of the adjacent pure stands of known chemical quality and one zero addition (blank) in open rings (20 cm inner diameter), which were covered with meshes to exclude fresh litter fall. Mass loss within two years amounted to 61-68% on Flysch and 36-44% on Molasse, indicating non-additive mixed species effects (mixed litter showed highest mass loss). However, base cation release showed a linear response, increasing from the spruce - over the mixed - to the beech litter. The differences in N release (immobilization) resulted in a characteristic converging trend in C/N ratios for all litter compositions on both bedrocks during decomposition. In the summers 2006 and 2007 we measured CO₂ efflux from these manipulated areas (a closed chamber fits exactly over such a ring) as field indicator of the microbial activity. Net fluxes (subtracting the so-called blank values) are considered an indicator of litter induced changes only and increased on both bedrocks from the spruce - over the mixed - to the beech litter. According to these measurements, decomposing litter contributed between 22-32% (Flysch) and 11-28% (Molasse) to total soil respiration, strengthening its role within the global carbon cycle.     

Interannual and interseasonal soil CO2 efflux and VOC exchange rates in a Mediterranean holm oak forest in response to experimental drought

Climate models predict drier conditions in the next decades in the Mediterranean basin. Given the importance of soil CO₂ efflux in the global carbon balance and the important role of soil monoterpene and volatile organic compounds (VOCs) in soil ecology, we aimed to study the effects of the predicted drought on soil CO₂, monoterpenes and other VOC exchange rates and their seasonal and interannual variations. We decreased soil water availability in a Mediterranean holm oak forest soil by means of an experimental drought system performed since 1999 to the present. Measurements of soil gas exchange were carried out with IRGA, GC and PTR-MS techniques during two annual campaigns of contrasting precipitation. Soil respiration was twice higher the wet year than the dry year (2.27±0.26 and 1.05±0.15, respectively), and varied seasonally from 3.76±0.85 μmol m⁻² s⁻¹ in spring, to 0.13±0.01 μmol m⁻² s⁻¹ in summer. These results highlight the strong interannual and interseasonal variation in CO₂ efflux in Mediterranean ecosystems. The drought treatment produced a significant soil respiration reduction in drought plots in the wet sampling period. This reduction was even higher in wet springs (43% average reduction). These results show (1) that soil moisture is the main factor driving seasonal and interannual variations in soil respiration and (2) that the response of soil respiration to increased temperature is constrained by soil moisture. The results also show an additional control of soil CO₂ efflux by physiology and phenology of trees and animals. Soil monoterpene exchange rates ranged from −0.01 to 0.004 nmol m⁻² s⁻¹, thus the contribution of this Mediterranean holm oak forest soil to the total monoterpenes atmospheric budget seems to be very low. Responses of individual monoterpenes and VOCs to the drought treatment were different depending on the compound. This suggests that the effect of soil moisture reduction in the monoterpenes and VOC exchange rates seems to be dependent on monoterpene and VOC type. In general, soil monoterpene and other VOC exchange rates were not correlated with soil CO₂ efflux. In all cases, only a low proportion of variance was explained by the soil moisture changes, since almost all VOCs increased their emission rates in summer 2005, probably due to the effect of high soil temperature. Results indicate thus that physical and biological processes in soil are controlling soil VOC exchange but further research is needed on how these factors interact to produce the observed VOCs exchange responses.     

Belowground carbon allocation patterns in a dry Mediterranean ecosystem: A comparison of two models

Total belowground C allocation (TBCA) accounts for a large fraction of gross primary production, it may overtake aboveground net primary production, and contributes to the primary source of detrital C in the mineral soil. Here, we measure soil respiration, water erosion, litterfall and estimate annual changes in C stored in mineral soil, litter and roots, in three representative land uses in a Mediterranean ecosystem (late-successional forest, abandoned agricultural field, rain-fed olive grove), and use two C balance approaches (steady-state and non-steady-state) to estimate TBCA. Both TBCA approaches are compared to assess how different C fluxes (outputs and inputs) affect our estimates of TBCA within each land use. In addition, annual net primary productivity is determined and C allocation patterns are examined for each land use. We hypothesized that changes in C stored in mineral soil, litter and roots will be slight compared to soil respiration, but will still have a significant effect on the estimates of TBCA. Annual net primary productivity was 648 ± 31.5, 541 ± 42.3 and 324 ± 22.3 g C m⁻² yr⁻¹ for forest, abandoned agricultural field and olive grove, respectively. Across land uses, more than 60% of the C was allocated belowground. Soil respiration (F_S) was the largest component in the TBCA approaches across all land uses. Annual C losses through water erosion were negligible compared to F_S (less than 1%) and had little effect on the estimates of TBCA. Annual changes in C stored in the soil, litter layer and roots were low compared to F_S (16, 24 and 10% for forest, abandoned agricultural field and olive grove, respectively), but had a significant effect on the estimates of TBCA. In our sites, an assumption that Δ[C_S + C_R + C_L]/Δt = 0 will underestimate TBCA, particularly in the abandoned agricultural field, where soil C storage may be increasing more rapidly. Therefore, the steady-state model is unsuited to these Mediterranean ecosystems and the full model is recommended.     

Grazing intensity alters soil respiration in an alpine meadow on the Tibetan plateau

Grazing intensity may alter the soil respiration rate in grassland ecosystems. The objectives of our study were to (1) determine the influence of grazing intensity on temporal variations in soil respiration of an alpine meadow on the northeastern Tibetan Plateau; and (2) characterise the temperature response of soil respiration under different grazing intensities. Diurnal and seasonal soil respiration rates were measured for two alpine meadow sites with different grazing intensities. The light grazing (LG) meadow site had a grazing intensity of 2.55 sheep ha⁻¹, while the grazing intensity of the heavy grazing (HG) meadow site, 5.35 sheep ha⁻¹, was approximately twice that of the LG site. Soil respiration measurements showed that CO₂ efflux was almost twice as great at the LG site as at the HG site during the growing season, but the diurnal and seasonal patterns of soil respiration rate were similar for the two sites. Both exhibited the highest annual soil respiration rate in mid-August and the lowest in January. Soil respiration rate was highly dependent on soil temperature. The Q₁₀ value for annual soil respiration was lower for the HG site (2.75) than for the LG site (3.22). Estimates of net ecosystem CO₂ exchange from monthly measurements of biomass and soil respiration revealed that during the period from May 1998 to April 1999, the LG site released 2040 g CO₂ m⁻² y⁻¹ to the atmosphere, which was about one third more than the 1530 g CO₂ m⁻² y⁻¹ released at the HG site. The results suggest that (1) grazing intensity alters not only soil respiration rate, but also the temperature dependence of soil CO₂ efflux; and (2) soil temperature is the major environmental factor controlling the temporal variation of soil respiration rate in the alpine meadow ecosystem.     

雷竹凋落叶不同分解环境中土壤动物群落特征

为研究火烧迹地雷竹(Phyllostachys violascens)凋落叶分解过程中土壤动物群落特征,以毗邻雷竹林为对照,采用凋落物袋法研究雷竹凋落叶分解速率及土壤动物群落结构的变化特征.结果显示,两个样地雷竹凋落叶分解过程总体上可以划分为3个阶段,即分解初期(质量损失率较高)、分解中期(凋落叶的质量损失率较上阶段减...     

Partitioning root and microbial contributions to soil respiration in Leymus chinensis populations

Based on the enclosed chamber method, soil respiration measurements of Leymus chinensis populations with four planting densities (30, 60, 90 and 120 plants/0.25 m²) and blank control were made from July 31 to November 24, 2003. In terms of soil respiration rates of L. chinensis populations with four planting densities and their corresponding root biomass, linear regressive equations between soil respiration rates and dry root weights were obtained at different observation times. Thus, soil respiration rates attributed to soil microbial activity could be estimated by extrapolating the regressive equations to zero root biomass. The soil microbial respiration rates of L. chinensis populations during the growing season ranged from 52.08 to 256.35 mg CO₂ m⁻² h⁻¹. Soil microbial respiration rates in blank control plots were also observed directly, ranging from 65.00 to 267.40 mg CO₂ m⁻² h⁻¹. The difference of soil microbial respiration rates between the inferred and the observed methods ranged from −26.09 to 9.35 mg CO₂ m⁻² h⁻¹. Some assumptions associated with these two approaches were not completely valid, which might result in this discrepancy. However, these two methods' application could provide new insights into separating root respiration from soil microbial respiration. The root respiration rates of L. chinensis populations with four planting densities could be estimated based on measured soil respiration rates, soil microbial respiration rates and corresponding mean dry root weight, and the highest values appeared at the early stage, then dropped off rapidly and tended to be constant after September 10. The mean proportions of soil respiration rates of L. chinensis populations attributable to the inferred and the observed root respiration rates were 36.8% (ranging from 9.7 to 52.9%) and 30.0% (ranging from 5.8 to 41.2%), respectively. Although root respiration rates of L. chinensis populations declined rapidly, the proportion of root respiration to soil respiration still increased gradually with the increase of root biomass.