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1.
The direct H2Oliquid–H2Ovapour equilibration method utilizing laser spectroscopy (DVE-LS) is a way to measure soil pore water stable isotopes. Various equilibration times and calibration methods have been used in DVE-LS. Yet little is known about their effects on the accuracy of the obtained isotope values. The objective of this study was to evaluate how equilibration time and calibration methods affect the accuracy of DVE-LS. We did both spiking and field soil experiments. For the spiking experiment, we applied DVE-LS to four soils of different textures, each of which was subjected to five water contents and six equilibration times. For the field soil experiment, we applied three calibration methods for DVE-LS to two field soil profiles, and the results were compared with cryogenic vacuum distillation (CVD)-LS. Results showed that DVE-LS demonstrated higher δ2H and δ18O as equilibration time increased, but 12 to 24 hr could be used as optimal equilibration time. For field soil samples, DVE-LS with liquid waters as standards led to significantly higher δ2H and δ18O than CVD-LS, with root mean square error (RMSE) of 8.06‰ for δ2H and 0.98‰ for δ18O. Calibration with soil texture reduced RMSE to 3.53‰ and 0.72‰ for δ2H and δ18O, respectively. Further, calibration with both soil texture and water content decreased RMSE to 3.10‰ for δ2H and 0.73‰ for δ18O. Our findings conclude that the calibration method applied may affect the measured soil water isotope values from DVE-LS.  相似文献   

2.
Measurements of δ2H and δ18O composition of pore waters in saturated and unsaturated soil samples are routinely performed in hydrological studies. A variety of in‐situ and lab‐based pore water extraction methods for the analysis of the stable isotopes of water now exist. While some have been used for decades (e.g. cryogenic vacuum extraction) others are relatively new, such as direct vapour equilibration or the microwave extraction technique. Despite their broad range of application, a formal and comprehensive intercomparison of soil water extraction methods for stable isotope analysis is lacking and long overdue. Here we present an intercomparison among five commonly used lab‐based pore water extraction techniques (high pressure mechanical squeezing, centrifugation, direct vapour equilibration, microwave extraction, and cryogenic extraction). We applied these extraction methods to two physicochemically different soil types that were dried and rewetted with water of known isotopic composition at three different water contents. Our results showed that the extraction approach can have a significant effect on pore water isotopic composition as all methods exhibited significant deviations from the spiked reference water, depending secondarily on the soil type and soil water content. Most pronounced, cryogenic water extraction showed large deviations from the spiked reference water, whereas mechanical squeezing and centrifugation provided results closest to the spiked water for both soil types. We also compared results for each extraction method – where liquid water was obtained – on both an OA‐ICOS and IRMS. Differences between these two analytical instruments were negligible for these organic compound‐free waters. We suggest that users of soil water extraction approaches carefully choose an extraction technique that is suitable for the specific research question, adapted to the dominant soil type and water content of the study. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

3.
Extracting water from soils is often a critical step for obtaining soil water isotope information. Cryogenic vacuum extraction (CVE), the most widely used laboratory-based removal technique, produces biased isotope composition and the mechanisms causing the biases remain uncertain. Here, we conducted spiking tests on soil samples oven-dried at 105 and 205°C, respectively. The recovery rate and isotopic composition of the extracted water were analysed. Our results show that conventional oven-drying (105°C) was not sufficient to liberate tightly bound water from soils but oven-drying at temperatures above 205°C was. Part of the tightly bound water in soil was extracted by CVE, because the extraction capacity of CVE (heating at 95°C) was equivalent to oven-drying at temperature between 105 and 205°C. Moreover, the two pretreatments yielded markedly differences in water recovery rates. And with increasing ratios of clay contents to water contents, the recovery rates of the pretreated soil at 105°C trended upward above 100%, but that of 205°C trended downward below 100%. Further, the 2H and 18O signatures of the extracted water from the soil pretreated at 205°C were both depleted relative to reference water, but the pretreatment at 105°C showed enriched 18O and depleted 2H. This suggests that oxygen isotope exchange may have occurred between tightly bound water and soil minerals, resulting in enriched 18O in water for the 105°C pretreatments. For the 205°C pretreatment, pre-existing soil water was completely removed and relative to spiking water, isotopic signatures of the extracted water followed equilibrium fractionation law due to incomplete extraction. Therefore, our results suggested that the biased isotopic signatures of water extracted by CVE may be partially due to incomplete extraction and mixture of added water with the residual tightly bound water that pre-exists before spiking.  相似文献   

4.
Spatio‐temporal heterogeneity in soil water content is recognized as a common phenomenon, but heterogeneity in the hydrogen and oxygen isotope composition of soil water, which can reveal processes of water cycling within soils, has not been well studied. New advances are being driven by measurement approaches allowing sampling with high density in both space and time. Using in situ soil water vapour probe techniques, combined with conventional soil and plant water vacuum distillation extraction, we monitored the hydrogen and oxygen stable isotopic composition of soil and plant waters at paired sites dominated by grasses and Gambel's oak (Quercus gambelii) within a semiarid montane ecosystem over the course of a growing season. We found that sites spaced only 20 m apart had profoundly different soil water isotopic and volumetric conditions. We document patterns of depth‐ and time‐explicit variation in soil water isotopic conditions at these sites and consider mechanisms for the observed heterogeneity. We found that soil water content and isotopic variability were damped under Q. gambelii, perhaps due in part to hydraulic redistribution of deep soil water or groundwater by Q. gambelii in these soils relative to the grass‐dominated site. We also found some support for H isotope discrimination effects during water uptake by Q. gambelii. In this ecosystem, the soil water content was higher than that at the neighbouring Grass site, and thus, 25% more water was available for transpiration by Q. gambelii compared with the Grass site. This work highlights the role of plants in governing soil water variation and demonstrates that they can also strongly influence the isotope ratios of soil water. The resulting fine‐scale heterogeneity has implications for the use of isotope tracers to study soil hydrology and evaporation and transpiration fluxes to improve understanding of water cycling through the soil–plant–atmosphere continuum.  相似文献   

5.
Water content and movement in soil profile and hydrogen isotope composition (δD) of soil water, rainwater, and groundwater were examined in a subalpine dark coniferous forest in the Wolong National Nature Reserve in Sichuan, China, following rainfall events in 2003–2004. Light rainfall increased water content in the litter and at soil depth of 0–80 cm, but the increased soil water was lost in several days. Heavy rainfall increased soil water content up to 85% at depths of 0–40 cm. Following the light rainfall in early spring, the δD of water from the litter, humus, illuvial, and material layers decreased first and then gradually reached the pre‐rainfall level. In summer, light rainfall reached the litter humus, and illuvial layer, but did not hit the material layer. Heavy rainfall affected δD of water in all layers. The δD of soil interflow slightly fluctuated with rainfall events. The δD of shallow groundwater did not differ significantly among all rainfall events. Light rainfall altered the shape of δD profile curve of water in the upper layer of soil, whereas heavy rainfall greatly affected the shape of δD profile curve of water in all soil layers. Following the heavy rainfall, preferential flow initially occurred through macropores, decayed plant roots, and rocks at different depths of soil profile. With continuing rainfall, the litter and surface soil were nearly saturated or fully saturated, and infiltration became homogeneous and plug‐like. Forest soil water, particularly in deeper soil profile, was slightly affected by rainfall and, thus, can be a source of water supply for regional needs, particularly during dry seasons. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

6.
The stable isotopes of hydrogen and oxygen (δ2H and δ18O) are useful conservative tracers for tracking the movement of water in soil. But although the tracking of water infiltrating through the soil profile and its movement as run‐off and groundwater recharge are well developed, water movement through the soil can also include evaporative fractionation. Soil water fractionation factors have, until now, been largely empirical. Unlike open water evaporation where temperature, humidity, and vapour pressure gradient define fractionation, soil water evaporation includes fractionation by soil matrix effects. These effects are still poorly characterized. Here, we present preliminary results from a simple laboratory experiment with four soil admixtures with grain sizes that range from sand to silt and clay. Our results show that soil tension seems to control the isotope fractionation of resident soil water. The relationship between soil tension and equilibrium fractionation appears to be independent of soil texture and appears well supported by thermodynamic theory. Although these results are preliminary, they suggest that future work should go after soil tension effects as a possible explanatory factor of soil water and water vapour fractionation.  相似文献   

7.
Soil water stable isotopes are widely used across disciplines (e.g., hydrology, ecology, soil science, and biogeochemistry). However, the full potential of stables isotopes as a tool for characterizing the origin, flow path, transport processes and residence times of water in different eco-, hydro-, and geological compartments has not yet been exploited. This is mainly due to the large variety of different methods for pore water extraction. While recent work has shown that matric potential affects the equilibrium fractionation, little work has examined how different water retention characteristics might affect the sampled water isotopic composition. Here, we present a simple laboratory experiment with two well-studied standard soils differing in their physico-chemical properties (e.g., clayey loam and silty sand). Samples were sieved, oven-dried and spiked with water of known isotopic composition to full saturation. For investigating the effect of water retention characteristics on the extracted water isotopic composition, we used pressure extractors to sample isotopically labelled soil water along the pF curve. After pressure extraction, we further extracted the soil samples via cryogenic vacuum extraction. The null hypothesis guiding our work was that water held at different tensions shows the same isotopic composition. Our results showed that the sampled soil water differed isotopically from the introduced isotopic label over time and sequentially along the pF curve. Our and previous studies suggest caution in interpreting isotope results of extracted soil water and a need to better characterize processes that govern isotope fractionation with respect to soil water retention characteristics. In the future, knowledge about soil water retention characteristics with respect to soil water isotopic composition could be applied to predict soil water fractionation effects under natural and non-stationary conditions. In this regard, isotope retention characteristics as an analog to water retention characteristics have been proposed as a way forward since matric potential affects the equilibrium fractionation between the bound water and the water vapour.  相似文献   

8.
Data on temporal variability in Mg isotope ratios of atmospheric deposition and runoff are critical for decreasing the uncertainty associated with construction of isotope mass balances in headwater catchments, and statistical evaluation of isotope differences among Mg pools and fluxes. Such evaluations, in turn, are needed to distinguish between biotic and abiotic contributions to Mg2+ in catchment runoff. We report the first annual time-series of δ26Mg values simultaneously determined for rainfall, canopy throughfall, soil water and runoff. The studied 55-ha catchment, situated in western Czech Republic, is underlain by Mg-rich amphibolite and covered by mature spruce stands. Between 1970 and 1996, the site received extremely high amounts of acid deposition and fly ash form nearby coal-burning power plants. The δ26Mg values of open-area precipitation (median of −0.79‰) at our study site were statistically indistinguishable from the δ26Mg values of throughfall (−0.73‰), but significantly different from the δ26Mg values of soil water (−0.55‰) and runoff (−0.55‰). The range of δ26Mg values during the observation period decreased in the order: open-area precipitation (0.57‰) > throughfall (0.27‰) > runoff (0.21‰) > soil water (0.16‰). The decreasing variability in δ26Mg values of Mg2+ from precipitation to soil water and runoff reflected an increasing homogenization of atmospheric Mg in the catchment and its mixing with geogenic Mg. In addition to atmospheric Mg, runoff also contained Mg mobilized from the three major solid Mg pools, bedrock (δ26Mg of −0.32‰), soil (−0.28‰), and vegetation (−0.31‰). The drought of summer 2019 did not affect the nearly constant δ26Mg value of runoff. Collectively, our data show that within-catchment processes buffer the Mg isotope variability of the atmospheric input.  相似文献   

9.
Here, we studied the isotope characteristics and source contributions of soil water in the permafrost active layer by collecting soil samples in July 2018 in Yangtze River basin. Soil moisture and temperature showed decreasing trends from 0–80 cm, and an increasing trend from 80–100 cm. The value of δ18O and δD first increased and then decreased in the soil profile of 0–100 cm; however, d-excess increased from 0–100 cm. δ18O values became gradually positive from the southwest to northeast of the study area, while d-excess gradually increased from southeast to northwest. The evaporation water line (EL) was δD = 7.56 δ18O + 1.50 (R2 = 0.90, p < 0.01, n = 96). Due to intense solar radiation and evaporation on the Tibetan Plateau, the elevation did not impact the surface soil. The altitude effect of the soil depths of 0–20 cm was not obvious, but the other soil layers had a significant altitude effect. Soil moisture and temperature were closely related to the stable isotopic composition of soil water. The contribution of precipitation to soil water on the sunny slope was 86%, while the contribution of the shady slope was 84%. However, the contribution of ground ice to soil water on sunny slope was 14% and the shady slope was 16%. The contribution of ground ice to soil water increased with increasing altitude on the sunny slope, but the contribution of ground ice to soil water had no obvious trend on the shady slope.  相似文献   

10.
Intercomparison of soil pore water extraction methods for stable isotope analysis has been a focus of recent studies in relation to plant source waters, which found a wide isotopic variance depending on the extraction method. Few studies have yet explored extraction effects for mobile pore waters that relate to hillslope runoff. This is because it is extremely difficult in natural systems to control the boundary conditions in order to assess and compare impacts of pore water extraction on resulting hillslope flow. With our new semicontrolled experiments on outdoor mini‐hillslopes, we studied mixing and runoff processes by means of stable isotopes of water and quantified relations between pore water extraction methods. We tested the null hypothesis that nondestructive and destructive pore water sampling methods sample the same soil water pool. Three hillslopes were mounted on load cells, filled with loamy sand textured soils from the Landscape Evolution Observatoryat Biosphere 2, equipped with soil moisture and temperature sensors, a bottom outflow, and a surface runoff gauge for isotope sampling. We followed the precipitation isotopic composition over and through the soil profile. One hillslope was instrumented with suction cups, on the second we installed sampling ports for in‐situ soil water vapour measurements, and the third hillslope was sampled destructively for applying the centrifugation and vapour equilibrium methods. All hillslopes were sampled at four depths (0–10, 10–20, 20–30, and 30–40 cm) at three different downslope positions. 2H and 18O analyses were performed via laser spectroscopy. We found no isotopic differences between rainfall, surface runoff, and bottom outflow. The in situ vapour ports' soil isotope data showed the widest spread over all hillslope positions and depths. Centrifugation's and suction cups' isotope results plotted closest to the local meteoric water line and within the range of hillslope runoff and bottom outflow data. Hillslope position did not influence the soil isotope results. These results suggest caution be used in the field when selecting an extraction technique for matching soil waters to runoff waters. Soil suction lysimeters and centrifugation appeared to be the most appropriate tools in this regard.  相似文献   

11.
Clay aquitards are semipermeable membranes that allow groundwater flow while retarding solute migration has been researched extensively but also subjected to much debate. At present, there is no evidence of whether the physical and chemical properties of clay soil and the isotopic composition of pore water affect the semipermeable membrane effect. In this study, we collected clay samples from drilling cores (30–90 m) in the Hengshui area located in the North China Plain (NCP), then extracted pore water using a high-pressure squeezing device. Vertical hydrochemical and isotopic profile variation trends for the pore water were revealed using hydrochemical (Cl−, Na+, Ca2+, K+, Mg2+, and SO42−) and stable isotopic measurements of H, O and Cl. The results showed that the hydrochemical clay interlayer pore water of the saline aquifer is Cl/SO4-Na/Mg type and the average total dissolved solids (TDS) are 10.17 g/L. However, the hydrochemical clay aquitard pore water is of the Cl/SO4-Na/Ca type with an average TDS of 1.90 g/L. The hydrochemical clay interlayer pore water of aquifer II is of Cl-Na/Ca type with an average TDS of 1.10 g/L. Our results showed that the water quality of the aquifer II is not affected by the upper part of the saline aquifer, thus the clay aquitard acts as a significant barrier to salt movement. A polarization layer concentrated in ions was formed between the upper part of the saline aquifer and the clay aquitard. The concentration polarization layer increases the salt-inhibition effect. H, O and Cl isotopic composition results showed significant fractionation. The pore water of aquifer II lacked heavy isotopes (2H, 18O, 37Cl), but had significant heavy isotope enrichment in the concentrated polarized layer (the δ2H value was −76‰, the δ18O value was −8.4‰, and the δ37Cl value was 1.59‰). Hyperfiltration thus played a significant role in isotope fractionation.  相似文献   

12.
Stable water isotope ratios are measured as a tracer of environmental processes in materials such as leaves, soils, and lakes. Water in these archives may experience evaporation, which increases the abundance of heavy isotopologues proportionally to the gradients in humidity and isotope ratio between the evaporating water and the surrounding atmosphere. The isotope ratio of the atmosphere has been difficult to measure until recently, and measurements remain scarce. As a result, several assumptions have been adopted to estimate isotope ratios of atmospheric water vapour. Perhaps the most commonly employed assumption in terrestrial environments is that water vapour is in isotopic equilibrium with precipitation. We evaluate this assumption using an eight‐member ensemble of general circulation model (GCM) simulations that include explicit calculation of isotope ratios in precipitation and vapour. We find that across the model ensemble, water vapour is typically less depleted in heavy isotopologues than expected if it were in equilibrium with annual precipitation. Atmospheric vapour likely possesses higher‐than‐expected isotope ratios because precipitation isotope ratios are determined by atmospheric conditions that favour condensation, which do not reflect atmospheric mixing and advection processes outside of precipitation events. The effect of this deviation on theoretical estimates of isotope ratios of evaporating waters scales with relative humidity. As a result, the equilibrium assumption gives relatively accurate estimates of the isotope ratios of evaporating waters in low latitudes but performs increasingly poorly at increasing latitudes. Future studies of evaporative water pools should include measurements of atmospheric isotope ratios or constrain potential bias with isotope‐enabled GCM simulations.  相似文献   

13.
Hanford Loam, from Richland, Washington, was used as a test soil to determine the precision, accuracy and nature of two methods to extract soil water for stable isotopic analysis: azeotropic distillation using toluene, and simple heating under vacuum. The soil was oven dried, rehydrated with water of known stable isotopic compositions, and the introduced water was then extracted.

Compared with the introduced water, initial aliquots of evolved water taken during a toluene extraction were as much as 30 ‰ more depleted in D and 2.7 ‰ more depleted in 18O, whereas final aliquots were as much as 40 ‰ more enriched in D and 14.3 ‰ more enriched in 18O. Initial aliquots collected during the vacuum/heat extraction were as much as 64 ‰ more depleted in D and 8.4 ‰ more depleted in 18O than was the introduced water, whereas the final aliquots were as much as 139 ‰ more enriched in D, and 20.8 ‰ more enriched in 18O. Neither method appears quantitative; however, the difference in stable isotopic composition between the first and last aliquots of water extracted by the toluene method is less than that from the vacuum/heat method. This is attributed to the smaller fractionation factors involved with the higher average temperatures of distillation of the toluene. The average stable isotopic compositions of the extracted water varied from that of the introduced water by up to 1.4 ‰ in δD and 4.2 ‰ in δ18O with the toluene method, and by 11.0 ‰ in δD and 1.8 ‰ in δ18O for the vacuum/heat method.

The lack of accuracy of the extraction methods is thought to be due to isotopic fractionation associated with water being weakly bound (not released below 110°C) in the soil. The isotopic effect of this heat-labile water is larger at low water contents (3.6 and 5.2% water by weight) as the water bound in the soil is a commensurately larger fraction of the total. With larger soilwater contents the small volume of water bound with an associated fractionation is not enough to affect the remaining unbound introduced soil water. Pretreatment of the soil to equilibrate the heat-labile water to the test water produced good results for the toluene distillation but not the vacuum/heat extraction method.

Vapors collected over the soils also show stable isotopic variations related to soilwater content. These vapors also appear to be in closer equilibrium with the free water, as extracted by the toluene method, than with the originally introduced water; thus, the soil vapors do not appear to be isotopically affected by the heat-labile water.

The toluene method appears to be better for extracting soil water for stable isotopic analysis because it allows more precise temperature control and excludes the extraction of heat-labile water which is isotopically fractionated. The bound nature of this heat-labile water limits association with the hydrologically active soil water; thus, the exclusion of this water from the soil water attained by toluene distillation may be advantageous. However, the azeotropic nature of toluene distillation affords no benefit and the extraction procedure must continue to completion.  相似文献   


14.
Subalpine forests are hydrologically important to the function and health of mountain basins. Identifying the specific water sources and the proportions used by subalpine forests is necessary to understand potential impacts to these forests under a changing climate. The recent “Two Water Worlds” hypothesis suggests that trees can favour tightly bound soil water instead of readily available free-flowing soil water. Little is known about the specific sources of water used by subalpine trees Abies lasiocarpa (Subalpine fir) and Picea engelmannii (Engelmann spruce) in the Canadian Rocky Mountains. In this study, stable water isotope (δ18O and δ2H) samples were obtained from S. fir and Engelmann spruce trees at three points of the growing season in combination with water sources available at time of sampling (snow, vadose zone water, saturated zone water, precipitation). Using the Bayesian Mixing Model, MixSIAR, relative source water proportions were calculated. In the drought summer examined, there was a net loss of water via evapotranspiration from the system. Results highlighted the importance of tightly vadose zone, or bound soil water, to subalpine forests, providing insights of future health under sustained years of drought and net loss in summer growing seasons. This work builds upon concepts from the “Two Water Worlds” hypothesis, showing that subalpine trees can draw from different water sources depending on season and availability. In our case, water use was largely driven by a tension gradient within the soil allowing trees to utilize vadose zone water and saturated zone water at differing points of the growing season.  相似文献   

15.
Soil moisture and its isotopic composition were observed at Spasskaya Pad experimental forest near Yakutsk, Russia, during summer in 1998, 1999, and 2000. The amount of soil water (plus ice) was estimated from volumetric soil water content obtained with time domain reflectometry. Soil moisture and its δ18O showed large interannual variation depending on the amount of summer rainfall. The soil water δ18O decreased with soil moisture during a dry summer (1998), indicating that ice meltwater from a deeper soil layer was transported upward. On the other hand, during a wet summer (1999), the δ18O of soil water increased due to percolation of summer rain with high δ18O values. Infiltration after spring snowmelt can be traced down to 15 cm by the increase in the amount of soil water and decrease in the δ18O because of the low δ18O of deposited snow. About half of the snow water equivalent (about 50 mm) recharged the surface soil. The pulse of the snow meltwater was, however, less important than the amount of summer rainfall for intra‐annual variation of soil moisture. Excess water at the time just before soil freezing, which is controlled by the amount of summer rainfall, was stored as ice during winter. This water storage stabilizes the rate of evapotranspiration. Soil water stored in the upper part of the active layer (surface to about 120 cm) can be a water source for transpiration in the following summer. On the other hand, once water was stored in the lower part of the active layer (deeper than about 120 cm), it would not be used by plants in the following summer, because the lower part of the active layer thaws in late summer after the plant growing season is over. Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

16.
Isotopic heterogeneity in soil water has hindered the application of isotope compositions (δ18O and δ2H) in soil water dynamics. This heterogeneity has been suggested to be caused by soil properties such as organic matter (OM) and clay content. However, this is yet to be verified in field soil. We sampled the organic layer (O-horizon soil) with highly decomposed organic material and the A-horizon soil in western Sichuan, China, and equilibrated these samples with vapour created by unconfined labelling water. The relationship between soil properties and isotopic fractionation (εT/U) between unconfined water and the total soil water was used to determine the line-conditioned excess (lc-excess) and source rain of A-horizon field soil by removing the influence of confined water. Equilibration experiments demonstrated a significant isotopic difference between the εT/U levels in the A-horizon and O-horizon soils, indicating that OM plays an important role in isotopic fractionation. In field samples, the lc-excess of the unconfined A-horizon water was, on an average, 2.5‰ higher than that of bulk soil water. The average offsets between the annual rain and the estimated source rain of soil water decreased by 5.0 and 0.5‰ for hydrogen and oxygen after removing the influence of confined water. Isotopic heterogeneity should not be ignored while examining the evaporation of soil water, soil source rain, and hence the recent ‘two water worlds’ hypothesis, which is especially true for cases in which the soils contain high levels of OM.  相似文献   

17.
Soils release more carbon, primarily as carbon dioxide (CO2), per annum than current global anthropogenic emissions. Soils emit CO2 through mineralization and decomposition of organic matter and respiration of roots and soil organisms. Given this, the evaluation of the effects of abiotic factors on microbial activity is of major importance when considering the mitigation of greenhouse gases emissions. Previous studies demonstrate that soil CO2 emission is significantly affected by temperature and soil water content. A limited number of studies have illustrated the importance of bulk density and soil surface characteristics as a result of exposure to rain on CO2 emission, however, none examine their relative importance. Therefore, this study investigated the effects of soil compaction and exposure of the soil surface to rainfall and their interaction on CO2 release. We conducted a factorial laboratory experiment with three soil types after sieving (clay, silt and sand soil), three different bulk densities (1·1 g cm–3, 1·3 g cm–3, 1·5 g cm–3) and three different exposures to rainfall (no rain, 30 minutes and 90 minutes of rainfall). The results demonstrated CO2 release varied significantly with bulk density, exposure to rain and time. The relationship between rain exposure and CO2 is positive: CO2 emission was 53% and 42% greater for the 90 minutes and 30 minutes rainfall exposure, respectively, compared to those not exposed to rain. Bulk density exhibited a negative relationship with CO2 emission: soil compacted to a bulk density of 1·1 g cm–3 emitted 32% more CO2 than soil compacted to 1·5 g cm–3. Furthermore we found that the magnitude of CO2 effluxes depended on the interaction of these two abiotic factors. Given these results, understanding the influence of soil compaction and raindrop impact on CO2 emission could lead to modified soil management practices which promote carbon sequestration. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

18.
Seasonal soil water dynamics were measured at a fine-textured, upslope site within the jarrah forest of southwest Western Australia and compared to the results from a coarse-textured hillslope transect. Gravity drainage dominated during winter and early spring. This reversed in early summer and an upward potential gradient was observed to 7 m depth. A shallow ephemeral saturation zone was observed above a clay pan at 1.5 m depth. This saturation zone persisted through late winter and early spring, contrasting with the short-lived saturation in the duricrust on the hillslope transect. The annual maximum to minimum unsaturated soil water storage was about 530 mm, 50 mm greater than the hillslope transect and higher than most values reported elsewhere in Australia. Significant soil water content changes following winter rain were generally restricted to 6 m but at one site occurred to 9 m. These depths were significantly less than the coarser-textured hillslope transect. Soil water drying rates averaged 5 mm day?1 during extended dry periods compared to 3.5 mm day?1 on the hillslope transect. The drying rate occurred uniformly through the profile until late summer when a significant decrease in the upper 3 m was observed.  相似文献   

19.
The stable isotopes of hydrogen and oxygen (δ2H and δ18O, respectively) have been widely used to investigate tree water source partitioning. These tracers have shed new light on patterns of tree water use in time and space. However, there are several limiting factors to this methodology (e.g., the difficult assessment of isotope fractionation in trees, and the labor-intensity associated with the collection of significant sample sizes) and the use of isotopes alone has not been enough to provide a mechanistic understanding of source water partitioning. Here, we combine isotope data in xylem and soil water with measurements of tree's physiological information including tree water deficit (TWD), fine root distribution, and soil matric potential, to investigate the mechanism driving tree water source partitioning. We used a 2 m3 lysimeter with willow trees (Salix viminalis) planted within, to conduct a high spatial–temporal resolution experiment. TWD provided an integrated response of plant water status to water supply and demand. The combined isotopic and TWD measurement showed that short-term variation (within days) in source water partitioning is determined mainly by plant hydraulic response to changes in soil matric potential. We observed changes in the relationship between soil matric potential and TWD that are matched by shifts in source water partitioning. Our results show that tree water use is a dynamic process on the time scale of days. These findings demonstrate tree's plasticity to water supply over days can be identified with high-resolution measurements of plant water status. Our results further support that root distribution alone is not an indicator of water uptake dynamics. Overall, we show that combining physiological measurements with traditional isotope tracing can reveal mechanistic insights into plant responses to changing environmental conditions.  相似文献   

20.
Widespread observations of ecohydrological separation are interpreted by suggesting that water flowing through highly conductive soil pores resists mixing with matrix storage over periods of days to months (i.e., two ‘water worlds’ exist). These interpretations imply that heterogeneous flow can produce ecohydrological separation in soils, yet little mechanistic evidence exists to explain this phenomenon. We quantified the separation between mobile water moving through preferential flow paths versus less mobile water remaining in the soil matrix after free-drainage to identify the amount of preferential flow necessary to maintain a two water world's scenario. Soil columns of varying macropore structure were subjected to simulated rainfall of increasing rainfall intensity (26 mm h−1, 60 mm h−1, and 110 mm h−1) whose stable isotope signatures oscillated around known baseline values. Prior to rainfall, soil matrix water δ2H nearly matched the known value used to initially wet the pore space whereas soil δ18O deviated from this value by up to 3.4‰, suggesting that soils may strongly fractionate 18O. All treatments had up to 100% mixing between rain and matrix water under the lowest (26 mm h−1) and medium (60 mm h−1) rainfall intensities. The highest rainfall intensity (110 mm h−1), however, reduced mixing of rain and matrix water for all treatments and produced significantly different preferential flow estimates between columns with intact soil structure compared to columns with reduced soil structure. Further, artificially limiting exchange between preferential flow paths and matrix water reduced bypass flow under the most intense rainfall. We show that (1) precipitation offset metrics such as lc-excess and d-excess may yield questionable interpretations when used to identify ecohydrological separation, (2) distinct domain separation may require extreme rainfall intensities and (3) domain exchange is an important component of macropore flow.  相似文献   

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