Spatial and seasonal variations in soil respiration in a temperate deciduous forest with fluctuating water table

Our objectives were to determine both spatial and temporal variations in soil respiration of a mixed deciduous forest, with soils exhibiting contrasting levels of hydromorphy. Soil respiration (R_S) showed a clear seasonal trend that reflected those of soil temperature (T_S) and soil water content (W_S), especially during summer drought. Using a bivariate model (RMSE=1.03), both optimal soil water content for soil respiration (W_SO) and soil respiration at both 10 °C and optimal soil water content (R_S10) varied among plots, ranging, respectively, from 0.25 to 0.40 and from 2.30 to 3.60 μmol m⁻² s⁻¹. Spatial variation in W_SO was related to bulk density and to topsoil N content, while spatial variation in R_S10 was related to basal area and the difference in pH measured in water or KCl suspensions. These results offer promising perspectives for spatializing ecosystem carbon budget at the regional scale.     

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.     

Temperature sensitivity of soil respiration in different ecosystems in China

Understanding the sensitivity of soil respiration to temperature change and its impacting factors is an important base for accurately evaluating the response of terrestrial carbon balance to future climatic change, and thus has received much recent attention. In this study, we synthesized 161 field measurement data from 52 published papers to quantify temperature sensitivity of soil respiration in different Chinese ecosystems and its relationship with climate factors, such as temperature and precipitation. The results show that the observed Q₁₀ value (the factor by which respiration rates increase for a 10 °C increase in temperature) is strongly dependent on the soil temperature measurement depth. Generally, Q₁₀ significantly increased with the depth (0 cm, 5 cm, and 10 cm) of soil temperature measuring point. Different ecosystem types also exhibit different Q₁₀ values. In response to soil temperature at the depth of 5 cm, alpine meadow and tundra has the largest Q₁₀ value with magnitude of 3.05 ± 1.06, while the Q₁₀ value of evergreen broadleaf forests is approximately half that amount (Q₁₀ = 1.81 ± 0.43). Spatial correlation analysis also shows that the Q₁₀ value of forest ecosystems is significantly and negatively correlated with mean annual temperature (R = −0.51, P < 0.001) and mean annual precipitation (R = −0.5, P < 0.001). This result not only implies that the temperature sensitivity of soil respiration will decline under continued global warming, but also suggests that such acclimation of soil respiration to warming should be taken into account in forecasting future terrestrial carbon cycle and its feedback to climate system.     

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.     

Microbial activity in soils frozen to below −39 °C

Recent research on life in extreme environments has shown that some microorganisms metabolize at extremely low temperatures in Arctic and Antarctic ice and permafrost. Here, we present kinetic data on CO₂ and ¹⁴CO₂ release from intact and ¹⁴C-glucose amended tundra soils (Barrow, Alaska) incubated for up to a year at 0 to −39°C. The rate of CO₂ production declined exponentially with temperature but it remained positive and measurable, e.g. 2-7 ng CO₂-C cm⁻³ soil d⁻¹, at −39 °C. The variation of CO₂ release rate (v) was adequately explained by the double exponential dependence on temperature (T) and unfrozen water content (W) (r²>0.98): v=A exp(λT+kW) and where A, λ and k are constants. The rate of ¹⁴CO₂ release from added glucose declined more steeply with cooling as compared with the release of total CO₂, indicating that (a) there could be some abiotic component in the measured flux of CO₂ or (b) endogenous respiration is more cold-resistant than substrate-induced respiration. The respiration activity was completely eliminated by soil sterilization (1 h, 121 °C), stimulated by the addition of oxidizable substrate (glucose, yeast extract), and reduced by the addition of acetate, which inhibits microbial processes in acidic soils (pH 3-5). The tundra soil from Barrow displayed higher below-zero activity than boreal soils from West Siberia and Sweden. The permafrost soils (20-30 cm) were more active than the samples from seasonally frozen topsoil (0-10 cm, Barrow). Finding measurable respiration to −39 °C is significant for determining, understanding, and predicting current and future CO₂ emission to the atmosphere and for understanding the low temperature limits of microbial activity on the Earth and on other planets.     

Response of soil respiration to precipitation during the dry season in two typical forest stands in the forest-grassland transition zone of the Loess Plateau

Forest ecosystems on the Loess Plateau are receiving increasing attention for their special importance in carbon fixation and conservation of soil and water in the region. Soil respiration was investigated in two typical forest stands of the forest-grassland transition zone in the region, an exotic black locust (Robinia pseudoacacia) plantation and an indigenous oak (Quercus liaotungensis) forest, in response to rain events (27.7 mm in May 2009 and 19 mm in May 2010) during the early summer dry season. In both ecosystems, precipitation significantly increased soil moisture, decreased soil temperature, and accelerated soil respiration. The peak values of soil respiration were 4.8 and 4.4 μmol CO₂ m⁻² s⁻¹ in the oak plot and the black locust plot, respectively. In the dry period after rainfall, the soil moisture and respiration rate gradually decreased and the soil temperature increased. Soil respiration rate in black locust stand was consistently less than that in oak stand, being consistent with the differences in C, N contents and fine root mass on the forest floor and in soil between the two stands. However, root respiration (R_r) per unit fine root mass and microbial respiration (R_m) per unit the amount of soil organic matter were higher in black locust stand than in oak stand. Respiration by root rhizosphere in black locust stand was the dominant component resulting in total respiration changes, whereas respiration by roots and soil microbes contributed equally in oak stand. Soil respiration in the black locust plantation showed higher sensitivity to precipitation than that in the oak forest.     

Temporal change in spatial variability of soil respiration on a slope of Japanese cedar (Cryptomeria japonica D. Don) forest

Although information regarding the spatial variability of soil respiration is important for understanding carbon cycling and developing a suitable sampling design for estimating average soil respiration, it remains relatively understudied compared to temporal changes. In this study, soil respiration was measured at 35 locations by season on a slope of Japanese cedar forest in order to examine temporal changes in the spatial distribution of soil respiration. Spatial variability of soil respiration varied between seasons, with the highest coefficient variation in winter (42%) and lowest in summer (26%). Semivariogram analysis and kriged maps revealed different patterns of spatial distribution in each season. Factors affecting the spatial variability were relief index (autumn), soil hardness of the A layer (winter), soil hardness at 50 cm depth (spring) and the altitude and relief index (summer). Annual soil respiration (average: 39 mol m⁻² y⁻¹) varied from 26 mol m⁻² y⁻¹ to 55 mol m⁻² y⁻¹ between the 35 locations and was higher in the upper part of the slope and lower in the lower part. The average Q₁₀ value was 2.3, varying from 1.3 to 3.0 among the locations. These findings suggest that insufficient information on the spatial variability of soil respiration and imbalanced sampling could bias estimates of current and future carbon budgets.     

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.     

Nitrogen addition stimulates different components of soil respiration in a subtropical bamboo ecosystem

Soil respiration is an important carbon (C) flux of global C cycle, and greatly affected by nitrogen (N) addition in the form of deposition or fertilization. However, the effects of N addition on the different components of soil respiration are poorly understood. The aim of this study is to investigate how the components of soil respiration response to N addition and the potential mechanisms in a subtropical bamboo ecosystem. Four N treatment levels (0, 50, 150, 300 kg N ha⁻¹ year⁻¹) were applied monthly in a Pleioblastus amarus bamboo plantation since November 2007. Total soil respiration (RS_T) and soil respiration derived from litter layer (RS_L), root-free soil (RS_S), and plant roots (RS_R) were measured for one year (February 2010 to January 2011). The results showed that the mean rate of RS_T was 428 ± 11 g C m⁻² year⁻¹, and RS_L, RS_S, RS_R contributed (30.2 ± 0.7)%, (20.7 ± 0.9)%, and (49.1 ± 0.7)%, respectively. The temperature coefficients (Q₁₀) of RS_T, RS_L, RS_S, and RS_R were 2.87, 2.28, 3.09, and 3.19, respectively, in control plots. Nitrogen additions significantly increased RS_T and its three components. RS_R was stimulated by N additions through increasing fine root biomass and root metabolic rate. The positive effects of N additions on soil fertility, microbial activity, and the quality and amount of aboveground litterfall also stimulated other CO₂ production processes. In the background of increased N input, response of RS_T and components of RS_T are primarily due to the positive response of plant growth in this bamboo ecosystem.     

Ozone deposition onto bare soil: A new parameterisation

The variables controlling ozone deposition onto bare soil are still unknown and it is necessary to understand this pathway well, as it represents a significant sink for ozone. Eddy-covariance measurements of ozone (O₃) fluxes were performed over bare soils in agricultural land. Three datasets with contrasted meteorological conditions and soil nitric oxide (NO) emissions were used to study the factors controlling soil deposition. It is considered that ozone deposition can be represented with an aerodynamic resistance (R_a), a quasi-laminar boundary layer resistance (Rb O₃), and an additional resistance, named soil resistance (R_soil). Although it is assumed in previous studies that soil resistance is a function of soil water content (SWC) and could be considered constant as variation of SWC at monthly scale are generally weak, the results of this study indicate that SWC is not the main factor controlling R_soil which shows daily and hourly variations. The main factor controlling soil resistance is the surface relative humidity which is positively correlated with R_soil, contrary to non stomatal resistance onto canopies which show a negative correlation with relative humidity. The relationship between R_soil and the surface relative humidity is probably due to a decrease in the surface available for ozone deposition, due to an increasing adsorption of water molecules onto the ground with relative humidity. A new parameterisation of R_soil was established, where R_soil is a function of the surface relative humidity only (R_soil = R_{soil min} × e^(k×RH_surf), and R_{soil min} = 21 ± 1.01 s m⁻¹ and k = 0.024 ± 0.001, mean ± SD). The measured and parameterised ozone deposition velocities agree well when soil NO emissions are negligible. However, when there are large soil NO emissions, the parameterised ozone deposition strongly underestimates the measured deposition velocity even if the chemical destruction of ozone by reaction with NO in the air column was evaluated to be negligible. This suggests that soil NO emissions enhance soil ozone deposition by chemical reaction at or near the soil surface. The new parameterisation allows a better estimation of soil deposition, especially during daytime when R_soil is overestimated using previously published parameterisations. It is an important step towards a better parameterisation of the non-stomatal uptake of ozone.     

A single application of Cu to field soil has long-term effects on bacterial community structure, diversity, and soil processes

Long-term diversity-disturbance responses of soil bacterial communities to copper were determined from field-soils (Spalding; South Australia) exposed to Cu in doses ranging from 0 through to 4012 mg Cu kg⁻¹ soil. Nearly 6 years after application of Cu, the structure of the total bacterial community showed change over the Cu gradient (PCR-DGGE profiling). 16S rRNA clone libraries, generated from unexposed and exposed (1003 mg Cu added kg⁻¹ soil) treatments, had significantly different taxa composition. In particular, Acidobacteria were abundant in unexposed soil but were nearly absent from the Cu-exposed sample (P<0.05), which was dominated by Firmicute bacteria (P<0.05). Analysis of community profiles of Acidobacteria, Bacillus, Pseudomonas and Sphingomonas showed significant changes in structural composition with increasing soil Cu. The diversity (Simpsons index) of the Acidobacteria community was more sensitive to increasing concentrations of CaCl-extractable soil Cu (Cu_Ext) than other groups, with decline in diversity occurring at 0.13 Cu_Ext mg kg⁻¹ soil. In contrast, diversity in the Bacillus community increased until 10.4 Cu_Ext mg kg⁻¹ soil, showing that this group was 2 orders of magnitude more resistant to Cu than Acidobacteria. Sphingomonas was the most resistant to Cu; however, this group along with Pseudomonas represented only a small percentage of total soil bacteria. Changes in bacterial community structure, but not diversity, were concomitant with a decrease in catabolic function (BioLog). Reduction in function followed a dose-response pattern with Cu_Ext levels (R²=0.86). The EC₅₀ for functional loss was 0.21 Cu_Ext mg kg⁻¹ soil, which coincided with loss of Acidobacteria diversity. The microbial responses were confirmed as being due to Cu and not shifts in soil pH (from use of CuSO₄) as parallel Zn-based field plots (ZnSO₄) were dissimilar. Changes in the diversity of most bacterial groups with soil Cu followed a unimodal response - i.e. diversity initially increased with Cu addition until a critical value was reached, whereupon it sharply decreased. These responses are indicative of the intermediate-disturbance-hypothesis, a macroecological theory that has not been widely tested in environmental microbial ecosystems.     

Soil CO2 flux in six monospecific forest plantations in Southern Rwanda

Forest soils contain the largest carbon stock of all terrestrial biomes and are probably the most important source of carbon dioxide (CO₂) to atmosphere. Soil CO₂ fluxes from 54 to 72-year-old monospecific stands in Rwanda were quantified from March 2006 to December 2007. The influences of soil temperature, soil water content, soil carbon (C) and nitrogen (N) stocks, soil pH, and stand characteristics on soil CO₂ flux were investigated. The mean annual soil CO₂ flux was highest under Eucalyptus saligna (3.92 μmol m⁻² s⁻¹) and lowest under Entandrophragma excelsum (3.13 μmol m⁻² s⁻¹). The seasonal variation in soil CO₂ flux from all stands followed the same trend and was highest in rainy seasons and lowest in dry seasons. Soil CO₂ flux was mainly correlated to soil water content (R² = 0.36-0.77), stand age (R² = 0.45), soil C stock (R² = 0.33), basal area (R² = 0.21), and soil temperature (R² = 0.06-0.17). The results contribute to the understanding of factors that influence soil CO₂ flux in monocultural plantations grown under the same microclimatic and soil conditions. The results can be used to construct models that predict soil CO₂ emissions in the tropics.     

Modeling vertical movement of organic matter in a soil incubated for 41 years with C labeled straw

The distribution of organic matter (OM) in the soil profile reflects the balance between inputs and decomposition at different depths as well as transport of OM within the profile. In this study we modeled movement of OM in the soil profile as a result of mechanisms resulting in dispersive and advective movement. The model was used to interpret the distribution of ¹⁴C in the soil profile 41 years after the labeling event. The model fitted the observed distribution of ¹⁴C well (R²=0.988, AIC_c=−82.6), with a dispersion constant of D=0.71 cm² yr⁻¹ and an advection constant of v=0.0081 cm yr⁻¹. However, the model consistently underestimated the amount of OM in the soil layers from 27 to 37 cm depth. A possible explanation for this is that different fractions of OM are transported by different mechanisms. For example, particulate OM, organomineral colloids and dissolved OM are not likely to be transported by the same mechanisms. A model with two OM fractions, one moving exclusively by dispersive processes (D=0.26 cm² yr⁻¹) and another moving by both dispersive (D=0.99 cm² yr⁻¹) and advective (v=0.23 cm yr⁻¹) processes provided a slightly better fit to the data (R²=0.995, AIC_c=−83.6). More importantly, however, this model did not show the consistent underestimation from 27 to 37 cm soil depth. This corroborates the assumption that differing movement mechanisms for different OM fractions are responsible for the observed distribution of ¹⁴C in the profile. However, varying dispersion, advection, and decay of OM with depth are also possible explanations.     

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.     

Influence of selenium on oxidoreductive enzymes activity in soil and in plants

The aim of this greenhouse experiment was the assessment of the influence of H₂SeO₃ at soil concentrations of 0.05, 0.15 and 0.45 mmol kg⁻¹, on the activity of selected oxidoreductive enzymes in wheat (Triticum aestivum). The wheat plants were grown in 2 dm³ pots filled with dust-silt black soil of pH 7.7. Applied H₂SeO₃ caused activation of plant nitrate reductase at all concentrations, but activation of plant polyphenol oxidase at only two lower concentrations. The highest concentration caused inhibition of polyphenol oxidase and peroxidase. Plant catalase activity decreased under the influence of 0.15 and 0.45 mmol kg⁻¹ concentration. After the final analysis Se was quantified in plants and soil. The amounts in plants were: control (unamended soil) 1.95 mg kg⁻¹; I dose (0.05 mmol kg⁻¹) 18.27 mg kg⁻¹; II dose (0.15 mmol kg⁻¹) 33.20 mg kg⁻¹ and III dose (0.45 mmol kg⁻¹) 38.37 mg kg⁻¹, in soil: 0.265 mg kg⁻¹; 3.61 mg kg⁻¹; 10.53 mg kg⁻¹; 30.53 mg kg⁻¹; respectively. Simultaneously, a laboratory experiment was performed, where the activity of soil catalase and peroxidase were tested after 1, 3, 7, 14, 28, 56, and 112 days after Se treatment. Peroxidase activity in soil decreased with increasing Se content, over the whole experiment. The lowest dose of Se caused activation a significant 10% increase in catalase activity, but the influence of others doses was unclear.     

Emission of N2O, N2 and CO2 from soil fertilized with nitrate: effect of compaction, soil moisture and rewetting

Soil compaction and soil moisture are important factors influencing denitrification and N₂O emission from fertilized soils. We analyzed the combined effects of these factors on the emission of N₂O, N₂ and CO₂ from undisturbed soil cores fertilized with (150 kg N ha⁻¹) in a laboratory experiment. The soil cores were collected from differently compacted areas in a potato field, i.e. the ridges (ρ_D=1.03 g cm⁻³), the interrow area (ρ_D=1.24 g cm⁻³), and the tractor compacted interrow area (ρ_D=1.64 g cm⁻³), and adjusted to constant soil moisture levels between 40 and 98% water-filled pore space (WFPS).High N₂O emissions were a result of denitrification and occurred at a WFPS≥70% in all compaction treatments. N₂ production occurred only at the highest soil moisture level (≥90% WFPS) but it was considerably smaller than the N₂O-N emission in most cases. There was no soil moisture effect on CO₂ emission from the differently compacted soils with the exception of the highest soil moisture level (98% WFPS) of the tractor-compacted soil in which soil respiration was significantly reduced. The maximum N₂O emission rates from all treatments occurred after rewetting of dry soil. This rewetting effect increased with the amount of water added. The results show the importance of increased carbon availability and associated respiratory O₂ consumption induced by soil drying and rewetting for the emissions of N₂O.     

Controls over pathways of carbon efflux from soils along climate and black spruce productivity gradients in interior Alaska

Small changes in C cycling in boreal forests can change the sign of their C balance, so it is important to gain an understanding of the factors controlling small exports like water-soluble organic carbon (WSOC) fluxes from the soils in these systems. To examine this, we estimated WSOC fluxes based on measured concentrations along four replicate gradients in upland black spruce (Picea mariana [Mill.] BSP) productivity and soil temperature in interior Alaska and compared them to concurrent rates of soil CO₂ efflux. Concentrations of WSOC in organic and mineral horizons ranged from 4.9 to 22.7 g C m⁻² and from 1.4 to 8.4 g C m⁻², respectively. Annual WSOC fluxes (4.5-12.0 g C m⁻² y⁻¹) increased with annual soil CO₂ effluxes (365-739 g C m⁻² y⁻¹) across all sites (R²=0.55, p=0.02), with higher fluxes occurring in warmer, more productive stands. Although annual WSOC flux was relatively small compared to total soil CO₂ efflux across all sites (<3%), its relative contribution was highest in warmer, more productive stands which harbored less soil organic carbon. The proportions of relatively bioavailable organic fractions (hydrophilic organic matter and low molecular weight acids) were highest in WSOC in colder, low-productivity stands whereas the more degraded products of microbial activity (fulvic acids) were highest in warmer, more productive stands. These data suggest that WSOC mineralization may be a mechanism for increased soil C loss if the climate warms and therefore should be accounted for in order to accurately determine the sensitivity of boreal soil organic C balance to climate change.     

Reductive transformation of pentachlorophenol on the interface of subtropical soil colloids and water

Ten soil colloids were obtained from three kinds of Fe-rich (> 50 g kg^− 1) subtropical soil parent materials (Basalt, Sandshale, and Quaternary Period Red Earth) collected in nine sites in Guangdong of China. Effect of the Fe-rich soil colloids and adding Fe(II) and oxalic acid on reductive dechlorination transformation of pentachlorophenol (PCP) were studied on colloids interfaces of reaction suspension. Mineralogical properties and specific surface area of the soil colloids were characterized by X-ray powder diffraction and Brunauer-Emmett-Teller (BET) methods, respectively. A series of reductive experiments were designed to determine PCP transformation and chloride ion release, and to calculate rate constant (k values) of pseudo first-order kinetics. Our results showed that reductive transformation of PCP occurred with k values from 0.007 to 0.057 d^− 1, and relevant chloride was released in the suspension of the ten soil colloids. Soil colloid developed from Basalt presented higher transformation rates (0.040-0.057 d^− 1) than that from Sandshale (0.007-0.033 d^− 1) and Quaternary Period red earth (0.012 d^− 1). Two paddy soil colloids developed from Sandshale (0.032-0.033 d^− 1) were more active than other three Sandshale soil colloids (0.007-0.011 d^− 1). The k values were significantly and positively correlated to the BET surface area (P < 0.01, n = 10). Addition of oxalic acid (0.022-0.231 d^− 1) or Fe(II) (0.029-0.256 d^− 1) into suspension of soil colloids gave arise to increase by 1.2-9.4 times in the k values. The release of chloride ion was simultaneously elevated. The enhancement of oxalic acid or Fe(II) on reductive transformation of PCP was attributed to increase of surface-bound Fe(II), which possess high reductive reactivity. The k values adding 1.0 mM oxalic acid were significantly and positively correlated to BET surface area and soil pH (P < 0.01), while k values adding 1.0 mM Fe(II) were related to total Fe (P < 0.001). The results may give new insight to understand the contribution of PCP abiotic reductive transformation in subtropical and tropical soils, and also in permeable reactive barriers.     

Changes in soil biological and biochemical characteristics in a long-term field trial on a sub-tropical inceptisol

Soil organic carbon (SOC), microbial biomass carbon (MBC), their ratio (MBC/SOC) which is also known as microbial quotient, soil respiration, dehydrogenase and phosphatase activities were evaluated in a long-term (31 years) field experiment involving fertility treatments (manure and inorganic fertilizers) and a maize (Zea mays L.)-wheat (Triticum aestivum L.)-cowpea (Vigna unguiculata L.) rotation at the Indian Agricultural Research Institute near New Delhi, India. Applying farmyard manure (FYM) plus NPK fertilizer significantly increased SOC (4.5-7.5 g kg⁻¹), microbial biomass (124-291 mg kg⁻¹) and microbial quotient from 2.88 to 3.87. Soil respiration, dehydrogenase and phosphatase activities were also increased by FYM applications. The MBC response to FYM+100% NPK compared to 100% NPK (193 vs. 291 mg kg⁻¹) was much greater than that for soil respiration (6.24 vs. 6.93 μl O₂ g⁻¹ h⁻¹) indicating a considerable portion of MBC in FYM plots was inactive. Dehydrogenase activity increased slightly as NPK rates were increased from 50% to 100%, but excessive fertilization (150% NPK) decreased it. Acid phosphatase activity (31.1 vs. 51.8 μg PNP g⁻¹ h⁻¹) was much lower than alkali phosphatase activity (289 vs. 366 μg PNP g⁻¹ h⁻¹) in all treatments. Phosphatase activity was influenced more by season or crop (e.g. tilling wheat residue) than fertilizer treatment, although both MBC and phosphatase activity were increased with optimum or balanced fertilization. SOC, MBC, soil respiration and acid phosphatase activity in control (no NPK, no manure) treatment was lower than uncultivated reference soil, and soil respiration was limiting at N alone or NP alone treatments.     

Surface soil hydraulic properties in four soil series under different land uses and their temporal changes

The concepts of “genoform” and “phenoform” distinguish the genetically-defined soil series and the variation of soil properties resulted from different land uses and management practices. With the repeated field measurements over time, we attempted to understand the difference of soil hydraulic properties among different land uses for a given soil series, and their temporal dynamics. Four soil series (Glenelg, Hagerstown, Joanna, and Morrison) in Pennsylvania with contrasting textures, structures, and parent materials were investigated. Within each soil series, four common land uses (woodland, cropland, pasture, and urban) were examined. At each site of soil series–land use combination, field-saturated and near-saturated hydraulic conductivities, K(ψ), were measured at the soil surface using standard tension infiltrometers at water supply potentials (ψ) of − 0.12, − .06, − 0.03, − 0.02, − 0.01, and 0 m. Surface infiltration measurements were repeated at each site in May and October from 2004 to 2006. The analysis of variance indicated that the measurement time (May or October) had the greatest impact on all measured hydraulic conductivities (p < 0.001), followed by the land use (p < 0.05 for K_ψ = 0 and K_{ψ = − 0.06}) and soil series (p < 0.06 for K_{ψ = − 0.01} to K_{ψ = − 0.03}). The interactions between the time and land use and between the soil series and land use were statistically significant for K_ψ = 0 and K_{ψ = − 0.01.} When separated by the measurement time, land use showed greater impacts in October than in May, while soil series had greater impacts in May than in October. Among the four land uses, woodland showed less obvious temporal change compared to the other three land uses because of less human-induced impacts and more consistent ground cover. Other three land uses generally showed a higher hydraulic conductivity in May than in October due to the drier initial soil moisture condition and related management practices in the spring that gave rise to more significant macropore flow. The results suggested that the initial soil moisture is an important variable that drives the temporal variation of the surface soil hydraulic properties.