Chromium transformation driven by iron redox cycling in basalt-derived paddy soil with high geological background values

The flooding and drainage of paddy fields has great effects on the transformation of heavy metals, however, the transformation of Cr in basalt-derived paddy soil with high geological background values was less recognized. The typical basalt-derived paddy soil was incubated under alternating redox conditions. The Cr fractions and the dynamics of Fe/N/S/C were examined. The HCl-extractable Cr increased under anaerobic condition and then decreased during aerobic stage. The UV-vis spectra of the supernatant showed that amounts of colloids were released under anaerobic condition, and then re-aggregated during aerobic phase. The scanning transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) revealed that Fe oxides were reduced and became dispersed during anaerobic stage, whereas Fe(II) was oxidized and recrystallized under aerobic condition. Based on these results, a kinetic model was established to further distinguish the relationship between the transformation of Cr and Fe. During anaerobic phase, the reduction of Fe(III) oxides not only directly released the structurally bound Cr, but also enhanced the breakdown of soil aggregation and dissolution of organic matter causing indirect mobilization of Cr. During aerobic phase, the oxidation of Fe(II) and further recrystallization of newly formed Fe(III) oxides might induce the re-aggregation of soil colloids and further incorporation of Cr. In addition, the kinetic model of Cr and Fe transformation was further verified in the pot experiment. The model-based findings demonstrated that the Cr transformation in the basalt-derived paddy soil with high geological background values was highly driven by redox sensitive iron cycling.     

SPACSYS: Integration of a 3D root architecture component to carbon, nitrogen and water cycling—Model description

It is an ongoing challenge to develop and demonstrate management practices that increase the sustainability of agricultural systems. Soil carbon and nitrogen dynamics directly affect soil quality, crop productivity and environmental impacts. Root systems are central to the acquisition of water and nutrients by plants, but are also a major pathway for the inputs of carbon and nutrients to soil. The complexity of both biotic and abiotic interactions, combined with stochastic changes in root architecture, makes it difficult to understand below-ground dynamics on the basis of experimentation alone. The integration of dynamic models of above-ground growth, three-dimensional root system demography, and interactions between plants and the environment, into one single model is a major challenge because of the complexity of the systems.In order to understand the interaction between a plant and the environment, it is advantageous to develop a model framework to integrate submodels that simulate various plant and environmental components. The objective of this paper is to outline a mechanistic and process-based model, which is capable of simulating interactions among environmental conditions around plants, plant growth and development, nitrogen and carbon cycles, with a three-dimensional root system submodel as an interface.The model presented in this paper is a mixed dimensional, multi-layer, field scale, weather-driven and daily time-step dynamic simulation model. The current version includes a plant growth and development component, a nitrogen cycling component, a carbon cycling component, plus a soil water component that includes representation of water flow to field drains as well as downwards through the soil layers, together with a heat transfer component. The components themselves and linkage among components are designed using object-oriented techniques, which makes the model robust, understandable and reusable. The components are implemented in the C++ programming language, and inputs and outputs of all components are organised as a database in either Microsoft^® SQL Server 2000, Access 2000 or MySQL5.0. Root architecture is visualised by using the OpenGL graphics system. Preliminary validation with two separate experimental datasets shows that the model can reasonably simulate root systems, nitrogen cycling, water movement and plant growth.     

PHOSPHORUS ASSIMILATION IN A STREAM SYSTEM OF THE LAKE OKEECHOBEE BASIN1

ABSTRACT: The ability to predict how streams and wetlands retain phosphorus (P) is critical to the management of watersheds that contribute nutrients to adjacent aquatic systems such as lakes. Field and laboratory experiments were conducted to determine the P assimilatory capacity of a stream (Otter Creek) in the Taylor Creek/Nubbin Slough Basin located north of Lake Okeechobee, Florida. Dominant soils in this basin are sandy Spodosols; landuse is primarily dairy farms and beef cattle pastures. Estimates of P assimilation show that sediments assimilate approximately 5 percent of the P load. Phosphorus assimilation rates in the stream were estimated using first-order relationships based on the total P concentration of the water column as a function of distance from the primary source. This method assumes minimal lateral inputs. Stream lengths required for one turnover in P assimilation were estimated to be in the range of 3–16 km. Laboratory studies using intact sediment cores indicated a P assimilation rate of 0.025 m day^?1, and equilibrium P concentration of 0.16 ± 0.03 mg L^?1 in the water column. Dissolved P concentration gradients in the sediments showed upward flux of P at water column P concentration of <0.16 mg L^?1. Approximately 56–77 percent of the P assimilated in the above-ground vegetation during active growth was released or translocated within six months of senesence, suggesting short-term storage in above-ground vegetation. Bottom sediments and recalcitrant detrital plant tissue provide for long-term P assimilation in the creek. Although stream sediments have the potential to adsorb P, high flow rate and low contact period between water and sediment limits this process.     

DYNAMICS OF ADDED NITRATE AND PHOSPHATE COMPARED IN A NORTHERN CALIFORNIA WOODLAND STREAM1

ABSTRACT: Injections of NO₃ and PO₄ were made during September 1975 into Little Lost Man Creek, a small pristine stream in Redwood National Park, California. Chloride, a conservative constituent, was added in a known ratio to the nutrients. Nutrient loss at a downstream point was calculated using concentration of added Cl as a reference. Nitrate nitrogen (NO₃-N), added for 4 h, reached 920 μg/1 (above 5 μg/1 background) just below the injection point, but increased only to 405 μg/1 at 310 m downstream. The concentration decrease was attributed to dispersion and to uptake by stream biota. Percent of NO₃-N lost decreased with increasing concentration of NO₃-N. Phosphate phosphorus (PO₄-P) was added a week after the NO₃-N for 3 h, causing a concentration increase of 296 μg/1 (above 13 μg/1 background) just below the injection point, of 161 μg/1 at 90 m downstream, and of 98 μg/1 at 310 m. Percent loss of PO₄-P at downstream sites increased with increasing PO₄-P concentration and also for a short period after peak concentration occurred, but then decreased as PO₄-P concentration continued decreasing. Differences in stream response to added NO₃-N and PO₄-P are attributed to differing rates of reaction with biota and differing degrees of interaction with abiotic stream solids.     

ATMOSPHERIC CONTRIBUTIONS TO FOREST NUTRIENT CYCLING1

The atmosphere is a significant source of plant nutrients that partially replenishes losses due to timber harvesting. The relative importance of wet and dry deposition depends upon the specific nutrient and site. Nitrogen in bulk precipitation (wetfall and dryfall) is equivalent to at least 70 percent of the nitrogen incorporated annually in above-ground woody tissues of some temperate hardwood forests. Atmospheric sources of calcium and potassium supply between 20 and 40 percent of the nutrients sequestered in woody increments. Annual nutrient inputs in bulk precipitation can exceed removals associated with sawiog harvest over a rotation period. Atmospheric inputs of nitrogen are only slightly less than hydrologic losses immediately after timber harvesting. The deposition of nutrients is highly variable in both time and space; interpretations of nutrient inputs and forest management impacts require quantification of inputs for a variety of ecosystems over long periods of time.     

EFFECTS OF FOREST HERBICIDE APPLICATIONS ON STREAMWATER CHEMISTRY IN SOUTHWESTERN BRITISH COLUMBIA1

ABSTRACT: The herbicide glyphosate was applied to portions of two watersheds in southwestern British Columbia to kill vegetation that was competing with Pseudotsuga menziesii (Douglas-fir) plantations. This application had little significant effect on streamwater chemistry (K⁺, Na²⁺, Mg²⁺, Ca²⁺, Cl^-, NOs₃^-, NH₄⁺, PO4^3-, SO₄⁼, and SiO₂ concentrations, electrical conductivity, and pH) when vegetation cover in a watershed was reduced by 4%, but had significant (P>0.05) effects, which lasted for at least five years, when cover was reduced by 43%. In this case, most parameters increased in value following the application, with K⁺ and Mg²⁺ concentrations and pH values exhibiting the most prolonged increases and NO₃^- concentrations exhibiting the greatest percentage increases. Sulphate and dissolved SiO₂ concentrations decreased following the application. Streamwater chemical fluxes showed similar trends to concentrations except that changes in fluxes were less significant and no decreases were observed. Forest management induced losses of NO₃-N in streamwater during the first five post-treatment years in the study area decreased in the order: herbicide application (approximately 40 kg/ha) < clearcutting and slashburning (approximately 20 kg/ha) < clearcutting (approximately 10 kg/ha). In watersheds similar to those of the study area, herbicide application is likely to have a greater impact on streamwater chemistry, in general, than would clearcutting or clearcutting followed by slashburning.     

Biogeochemical characterisation of a coal tar distillate plume

The distillation of acidified coal tars for up to 50 years has given rise to a phenol plume approximately 500 m long, 50 m deep and containing up to 15 g l(-1) dissolved organic carbon (DOC) in the Triassic Sandstones aquifer. A conceptual biogeochemical model based on chemical and microbiological analysis of groundwater samples has been developed as a preliminary to more detailed studies of the controls on natural attenuation. While the development of redox zones and the production of methane and carbon dioxide provide evidence of natural attenuation, it appears that degradation is slow. The existence of sulphate in the plume indicates that this electron acceptor has not been depleted and that consequently methanogenesis is probably limited. Based on a simple estimate of sulphate input concentration, a half-life of about 15 years has been estimated for sulphate reduction. Geochemical modelling predicts that increased alkalinity within the plume has not led to carbonate precipitation, and thus within the limits of accuracy of the measurement, alkalinity may reflect the degree of biodegradation. This implies a loss of around 18% of the DOC over a 30-year period. Despite limited degradation, microbial studies show that there are diverse microbial communities in the aquifer with the potential for both anaerobic and aerobic biodegradation. Microbial activity was found to be greatest at the leading edge of the plume where DOC concentrations are 60 mg l(-1) or less, but activity could still be observed in more contaminated samples even though cells could not be cultured. The study suggests that degradation may be limited by the high phenol concentrations within the core of the plume, but that once diluted by dispersion, natural attenuation may proceed. More detailed studies to confirm these initial findings are identified and form the basis of associated papers.     

Engineered and subsequent intrinsic in situ bioremediation of a diesel fuel contaminated aquifer

A diesel fuel contaminated aquifer in Menziken, Switzerland was treated for 4.5 years by injecting aerated groundwater, supplemented with KNO3 and NH4H2PO4 to stimulate indigenous populations of petroleum hydrocarbon (PHC) degrading microorganisms. After dissolved PHC concentrations had stabilized at a low level, engineered in situ bioremediation was terminated. The main objective of this study was to evaluate the efficacy of intrinsic in situ bioremediation as a follow-up measure to remove PHC remaining in the aquifer after terminating engineered in situ bioremediation. In the first 7 months of intrinsic in situ bioremediation, redox conditions in the source area became more reducing as indicated by lower concentrations of SO4(2-) and higher concentrations of Fe(II) and CH4. In the core of the source area, strongly reducing conditions prevailed during the remaining study period (3 years) and dissolved PHC concentrations were higher than during engineered in situ bioremediation. This suggests that biodegradation in the core zone was limited by the availability of oxidants. In lateral zones of the source area, however, gradually more oxidized conditions were reestablished again, suggesting that PHC availability increasingly limited biodegradation. The total DIC production rate in the aquifer decreased within 2 years to about 25% of that during engineered in situ bioremediation and remained at that level. Stable carbon isotope analysis confirmed that the produced DIC mainly originated from PHC mineralization. The total rate of DIC and CH4 production in the source area was more than 300 times larger than the rate of PHC elution. This indicates that biodegradation coupled to consumption of naturally occurring oxidants was an important process for removal of PHC which remained in the aquifer after terminating engineered measures.     

Ce-based catalysts used in advanced oxidation processes for organic wastewater treatment: A review

Refractory organic pollutants in water threaten human health and environmental safety, and advanced oxidation processes (AOPs) are effective for the degradation of these pollutants. Catalysts play vital role in AOPs, and Ce-based catalysts have exhibited excellent performance. Recently, the development and application of Ce-based catalysts in various AOPs have been reported. Our study conducts the first review in this rapid growing field. This paper clarifies the variety and properties of Ce-based catalysts. Their applications in different AOP systems (catalytic ozonation, photodegradation, Fenton-like reactions, sulfate radical-based AOPs, and catalytic sonochemistry) are discussed. Different Ce-based catalysts suit different reaction systems and produce different active radicals. Finally, future research directions of Ce-based catalysts in AOP systems are suggested.     

干湿循环与垃圾渗滤液耦合作用下GCL防渗性能

开展膨胀指数和渗透系数测定试验,研究干湿循环与垃圾渗滤液渗透耦合作用下膨润土的膨胀性能和土工合成黏土衬垫（GCL）防渗性能变化规律.结果表明,干湿循环与垃圾渗滤液渗透耦合作用对膨润土的膨胀性能和GCL的防渗性能具有显著负面影响：在7次干湿循环后,垃圾渗滤液饱和的膨润土的膨胀指数从20mL/2g降低至7.5mL/2g,GCL的渗透系数从1.65×10^-11m/s增加到1.89×10^-7m/s.膨胀指数下降和渗透系数升高的根本原因是膨润土渗透膨胀性能的丧失.单纯的垃圾渗滤液渗透不会改变GCL的渗透系数.将有效应力从20kPa升高至150kPa,可以促使GCL的渗透系数降低4个数量级,满足填埋场防渗要求（< 5.0x10^-11m/s）.