Sewage sludge is a cost-effective media for the production of Bacillus thuringiensis (Bt) based biopesticides. To enhance the entomotoxicity of the fermentation broth, pretreatments of sewage sludge by alkali and ultrasonic were applied in this study. Effects of alkaline and ultrasonic pretreatments on the soluble COD (SCOD) and total COD (TCOD) were evaluated by altering the alkali addition dose and the ultrasonic specific energy. Suitable pretreatment conditions were optimized with 5 g l-¹ sodium hydroxide (NaOH) for alkaline treatment and 1.2 x 10⁵ kJ kg-¹ of total solid for ultrasonic treatment. Fermentations of raw and pretreated sludge for biopesticides were carried out in a bench scale fermentor. Results revealed that both pretreatments were effective for Bt growth and metabolism. Higher viable cells (VC) and viable spores (VS) counts, δ-endotoxin yields and entomotoxicity were achieved in the pretreated sludge. The enhancement was attributed to more available nutrients and better oxygen transfer. Moreover, ultrasonic pretreated sludge was superior to alkaline pretreated sludge for δ-endotoxin production and entomotoxicity owing to its higher soluble C/N ratio and finer particles.

The study of mineral components in respirable particles (particulate matter with diameter less than 10 μm, PM₁₀) in ambient air is important in understanding and improving air quality. In this study, PM₁₀ samples were collected in various areas around Beijing during 2002~2003, including an urban setting, a satellite city and a rural area. The mineralogical composition of these PM₁₀ samples was studied by X-ray diffraction (XRD), environmental scanning electron microscopy / and energy-dispersive X-ray analyzer (ESEM/EDX). The results indicated that mineral composition of PM₁₀ in different seasons and in different region varied significantly. Mineral mass concentration in Beijing PM₁₀ reached the highest percentage in the spring and fell to the lowest level in the autumn. The minerals in the spring PM₁₀ were dominated by clay minerals and quartz, followed by plagioclase, K-feldspar, calcite, dolomite, hematite, pyrite, magnesite, gypsum and laumontite as well as some unidentified materials. Fewer mineral types were collected in summer, however some new components, including K(NH₄)Ca(SO4)₂·H₂O, NH₄Cl and As₂O₃·SO₃ were noted to be present, suggesting that atmospheric chemical reaction in Beijing air were more active in summer than in other seasons. Mineral components in Beijing urban air were at a higher percentage with fewer phases than that in satellite city air. In conclusion, there was considerable variation in mineral components in PM₁₀ samples collected in different seasons and areas, which reflects the related air quality of sampling areas.

Long-term nutrient concentration trends and load variations at six monitoring stations on four canals in the Southern Indian River Lagoon (Florida, USA) were evaluated using the Estimate Trend (Estrend) and Load Estimator (Loadest) programs. The results of trend analysis on nutrient concentrations suggested that the nutrient trend patterns were spatially variable. Increasing trends were most often observed in orthophosphate and/or total phosphorus at five stations. Significantly increased annual loads were observed for orthophosphate at four stations from 1979 through 2004. The median concentrations of ammonia (0.05 to 0.10 mg l-¹) were greater than the State of Florida surface water quality criteria of class III freshwater body for ammonia. The median concentrations of total phosphorus (138 to 376 μg l-¹) were greater than the USEPA ambient water quality criteria recommendation for the study area (Nutrient Ecoregion XIII). Nutrient (phosphorus and nitrogen) loads observed in this study are likely to impair the water quality in the Southern Indian River Lagoon.

In principle, conventional lysimeters are suitable for the investigation of vertical water and solute fluxes. Lateral fluxes in water-saturated fen sites are characterized by heterogeneities and abnormities due to anisotropic layering. But due to lack of adequate monitoring techniques, these fluxes have been insufficiently analyzed. The newly developed large weighable fen lysimeter (LWFL) overcomes the limitations of conventional lysimetry and enables the measurement of vertical and horizontal transport processes in undisturbed large volume soil monoliths. The LWFL has a volume of 6 m³ (4 m length, 1 m width and 1.5 m depth) and was tested by filling the lysimeter with an undisturbed fen monolith. A special extraction procedure for the horizontal sliding of the lysimeter vessel through the natural fen was developed. In front of the vessel a converted cutting tool assisted in carving the soil monolith out of the peat, both vertically and horizontally. Inlet and outlet of the LWFL was constructed to allow the adjustment of a wide range of hydraulic gradients to depict natural occurring lateral transport processes. The LWFL including the measurement techniques was tested successfully for 3 years. On the basis of these tests, we conclude that complex physical and biogeochemical research problems involving lateral flows can be tackled now with multiphase observations and measurements at high spatial and temporal resolution, transdisciplinary data evaluation and numerical modelling approaches.

Trace elements may present an environmental hazard in the vicinity of mining and smelting activities. However, the factors controlling their distribution and transfer within the soil and vegetation systems are not always well defined. Total concentrations of up to 15,195 mg . kg –¹ As, 6,690 mg . kg–¹ Cu, 24,820 mg . kg–¹ Pb and 9,810 mg . kg–¹ Zn in soils, and 62 mg . kg–¹ As, 1,765 mg . kg–¹ Cu, 280 mg . kg–¹ Pb and 3,460 mg . kg –¹ Zn in vegetation were measured. However, unusually for smelters and mines of a similar size, the elevated trace element concentrations in soils were found to be restricted to the immediate vicinity of the mines and smelters (maximum 2–3 km). Parent material, prevailing wind direction, and soil physical and chemical characteristics were found to correlate poorly with the restricted trace element distributions in soils. Hypotheses are given for this unusual distribution: (1) the contaminated soils were removed by erosion or (2) mines and smelters released large heavy particles that could not have been transported long distances. Analyses of the accumulation of trace elements in vegetation (median ratios: As 0.06, Cu 0.19, Pb 0.54 and Zn 1.07) and the percentage of total trace elements being DTPA extractable in soils (median percentages: As 0.06%, Cu 15%, Pb 7% and Zn 4%) indicated higher relative trace element mobility in soils with low total concentrations than in soils with elevated concentrations.

Interactions between Zn and Cd on the accumulation of these metals in coontail, Ceratophyllum demersum were studied at different metal concentrations. Plants were grown in nutrient solution containing Cd (0.05–0.25 mg l⁻¹) and Zn (0.5–5 mgl⁻¹). High concentrations of Zn caused a significant decrease in Cd accumulation. In general, adding Cd solution decreased Zn accumulation in C. demersum except at the lowest concentration of Zn in which the Zn accumulation was similar to that without Cd. C. demersum could accumulate high concentrations of both Cd and Zn. The influence of humic acid (HA) on Cd and Zn accumulation was also studied. HA had a significant effect on Zn accumulation in plants. 2 mg l⁻¹ of HA reduced Zn accumulation at 1 mg l⁻¹ level (from 2,167 to 803 mg kg⁻¹). Cd uptake by plant tissue, toxicity symptoms and accumulation at 0.25 and 0.5 mg l⁻¹, were reduced (from 515 to 154 mg kg⁻¹ and from 816 to 305 mg kg⁻¹, respectively) by addition of 2 mg l⁻¹ of HA. Cd uptake reached a maximum on day 9 of treatment, while that of Zn was observed on day 15. Long-term accumulation study revealed that HA reduced toxicity and accumulation of heavy metals.

Drainage water from agricultural fields with applied manure can degrade the bacterial quality of surface and groundwater. The impact of conventional tillage (CT) and zero tillage (ZT) practices on Escherichia coli (E.coli) discharge through artificially drained soils is not well understood. Consequently, two field trials were conducted during 2002–2004. The first trial involved fall applications of beef manure while the second involved spring applications of dairy manure. Both surface and subsurface drainage water were monitored in the first trial while only subsurface drainage water was monitored in the second. Under fall applied beef manure (trial 1), no differences (p > 0.05) were observed in E.coli concentrations (cfu/100 ml) in combined drainage water under both tillage systems. However, during 2003–2004, subsurface drainage water under ZT had higher E.coli concentrations and loads than drainage water under CT. When the combined (surface + subsurface) annual E.coli loads were considered, CT loads were greater than ZT during 2002–2003 with an opposite situation during 2003–2004. Overall, annual E.coli loads were similar under ZT (4.7 × 10¹⁰ cfu/ha) and CT (4.8 × 10¹⁰ cfu/ha). Spring dairy manure application (trial 2) produced significant (p > 0.03) tillage effect on E.coli loads in subsurface drainage water only during the second year. During the study period, ZT plots (1.55 × 10¹⁰ cfu/ha) discharged 5× more E.coli than CT (0.23 × 10¹⁰ cfu/ha). A longer duration of ZT practices resulted in higher subsurface flow volumes and subsequently greater loads of E.coli discharge in both trials.

The representativeness of soil pore water extracted by suction lysimeters in ground-water monitoring studies is a problem that often confounds interpretation of measured data. Current soil water sampling techniques cannot delineate from which soil volume a pore water sample is extracted, neither macroscopic, microscopic, or preferential flowpath. This research was undertaken to compare δ¹⁸O and Br- values of extracted suction lysimeters samples from intact soil cores with samples obtained by the direct extraction methods of centrifugation and azeotropic distillation. Also, the study was concerned with determining what portion of soil pore water is sampled by each method and explaining differences in concentrations of the extracted water from each method to allow a determination of the accuracy and viability of the three methods of extraction. Intact soil cores (30 cm diameter by 40 cm height) were extracted from two different sites. Site 1 was rapid infiltration basin number 50, near Altamonte Springs in Seminole County, Florida. Site 2 was the Missouri Management System Evaluation Area (MSEA) near Centralia in Boone County, Missouri. Isotopically (¹⁸Oδ) labeled water and bromide concentrations within water samples taken by suction lysimeters was compared with samples obtained by methods of centrifugation and azeotropic distillation. The ¹⁸Oδ water was analyzed by mass spectrometry while bromide concentration, applied in the form of KBr was measured using standard IC procedures. Water collected by centrifugation and azeotropic distillation data were about 0.25[per thousand] more negative than that collected by suction lysimeter values from a sandy soil and about 2-7[per thousand] more negative from a well structured soil. Results indicate that the majority of soil water in well-structured soil is strongly bound to soil grain surfaces and is not easily sampled by suction lysimeters. In cases where a sufficient volume of water has passed through the soil profile and displaced previous pore water, suction lysimeters will collect a representative sample of soil pore water from the sampled depth interval. It is suggested that for stable isotope studies monitoring precipitation and soil water, suction lysimeter be installed at shallow depths (10 cm). Samples should also be coordinated with precipitation events. The data also suggest that each extraction method samples a separate component of soil-pore water. Centrifugation can be used with success, particularly for efficient sampling of large areas. Azeotropic distillation is more appropriate when strict qualitative and quantitative data on sorption desorption, and various types of kinetic studies may be needed.

Many lakes in the Adirondack Mountains, New York, have acidified over the past century due to acidic atmospheric deposition. More recently, most monitored lakes have shown signs of chemical recovery (increase in acid neutralizing capacity) as sulfur deposition levels have declined in response to the Clean Air Act and other emissions control legislation. We used measured and modeled trends in past lakewater acidification and projections of future recovery from acidification to extrapolate results from judgment samples of intensively studied lakes to the population of acid-sensitive Adirondack lakes. Simulations were developed for 70 watersheds using the Model of Acidification of Groundwater in Catchments (MAGIC) to classify lakes according to their sensitivity to change in atmospheric S and N deposition. MAGIC simulations suggested that the modeled Adirondack Long-Term Monitoring Project (ALTM) and Adirondack Effects Assessment Project (AEAP) lakes were largely among the lakes in the population that had acidified most between 1850 and 1990. Most of the modeled ALTM/AEAP lakes were within the top 36% of acid sensitivity, based on model projections of past acidification and future chemical recovery, compared with the 1,829 Adirondack lakes in EPA's Environmental Monitoring and Assessment Program (EMAP) statistical frame. Results of this research will allow fuller utilization of data from on-going chemical and biological monitoring and process-level studies by providing a basis for regionalization of findings and developing/refining relationships among watershed characteristics, chemical change, and biological responses to changing levels of acidic deposition.

According to recent insight, the toxicity of metals in soils is better related to the free metal ion (FMI) activity in the soil solution than to the total metal concentration in soil. However, the determination of FMI activities in soil solution is a difficult and time-consuming task. An alternative is to use empirical equations (so called transfer functions (TFs)) that relate FMI activity in solution to the reactive metal concentration in the solid phase and to soil properties (pH and organic matter content). Here we test the applicability of two sets of TF for Cd and Pb using independent data from a wide range of soil types and regions that are not represented in the datasets used to derive the TFs. From these soils, soil solution was extracted using four different methods. For all these extracts, FMI activities were calculated from total concentrations in solution using the speciation program WHAM VI. In some of the soils, Cd and Pb FMI activities were also measured using a Donnan membrane technique. Most of these FMI activities deviated from the TF predictions by less than one order of magnitude and were within the 95% confidence interval of the TFs, irrespective of the method used to extract soil solution. Predictability was higher for Pb than for Cd and differed also between the two TF sets.