Metal binding in soil cores and sediments in the vicinity of a dammed agricultural and industrial watershed

The environment is witnessing a downgrade caused by the amelioration of the industrial and agricultural sectors, namely, soil and sediment compartments. For those reasons, a comparative study was done between soil cores and sediments taken from two locations in the Qaraaoun reservoir, Lebanon. The soil cores were partitioned into several layers. Each layer was analyzed for several physicochemical parameters, such as functional groups, particle size distribution, ζ-potential, texture, pH, electric conductivity, total dissolved solids, organic matter, cation exchange capacity, active and total calcareous, available sodium and potassium, and metal content (cadmium, copper, and lead). The metal content of each site was linked to soil composition and characteristics. The two sites showed distinguishable characteristics for features such as organic matter, pH, mineral fraction, calcareous, and metal content. The samples taken toward the south site (Q1), though contain lower organic matter than the other but are more calcareous, showed higher metal content in comparison to the other site (Q2) (average metal content of Q1 > Q2; for Cd 3.8?>?1.8 mg/kg, Cu 28.6?>?21.9 mg/kg, Pb 26.7?>?19 mg/kg). However, the metal content in this study did not correlate as much to the organic matter; rather, it was influenced by the location of the samples with respect to the dam, the reservoir’s hydrodynamics, the calcareous nature of the soil, and the variation of the industrial and agricultural influence on each site.     

Polycyclic aromatic hydrocarbon in rain and street runoff in Amman, Jordan

Concentrations of polycyclic aromatic hydrocarbons(PAHs) were determined in the rain and street runoff samples from two sites in the vicinity of Amman City during the pluvial period 1999--2000. The results showed that elevated levels of PAHs were detected in the city center(site 1 ) than the residential area( site 2) and that the levels were higher in street runoff than rain samples of the same sites. The highest concentration of PAHs in both street runoff and rain samples were observed in the first rainy month( November 1999) which indicated a wash out effect of PAHs originating from vehicular emission accumulated during the long dry summer season before sampling. Within the investigated cold winter seasons, fluctuations in PAHs concentration were observed. The variation was attributed to the fossil combustion for heating purposes and to intervals between rainfalls: as the longer the intervals between rains were, the higher the PAH concentration were. Removal of PAHs from the atmosphere through precipitation over the investigated period varied with time and places depending on the amount of rainfall where higher rainfall removed higher amount of PAHs from the almosphere. The amount of PAHs washed out through precipitation was estimated to be around 14.8 mg/m^2 and 21.1 mg/m^2 for sites 1 and 2 respectively.     

Distribution of gamma-ray emitting radionuclides in the marine environment of the Burullus Lake: II. Bottom sediments

The sediment compartment has the ability to trap large amounts of radionuclides and to indicate the radiological impact of pollution. The present work shows the results obtained related to the concentrations of ¹³⁷Cs and natural radionuclides in sediment in the Burullus Lake, Egypt. The average values of ²²⁶Ra, ²³²Th, and ⁴⁰K in the bottom sediments collected from the east of the Burullus Lake ranged from 10.3 to 21.8 Bq/kg, from 11.9 to 34.4 Bq/kg, and from 268 to 401 Bq/kg, respectively. The study has shown that ⁴⁰K concentration is nearly uniform throughout the studied area while ²²⁶Ra and ²³²Th are more concentrated in the northeastern shore. Lake sediments showed contamination with ¹³⁷Cs (2.7–15.9 Bq/kg). The ¹³⁷Cs sediment activities indicated higher concentrations in the off-shore sites. Concentrations of all γ -ray emitting radionuclides except ⁴⁰K in water samples were below the detection limits. The ⁴⁰K sediment–water distribution coefficients of the near-shore samples were higher than the off-shore samples.     

Empirical gas emission and oxidation measurement at cover soil of dumping site: example from Malaysia

Methane (CH₄) is one of the most relevant greenhouse gases and it has a global warming potential 25 times greater than that of carbon dioxide (CO₂), risking human health and the environment. Microbial CH₄ oxidation in landfill cover soils may constitute a means of controlling CH₄ emissions. The study was intended to quantify CH₄ and CO₂ emissions rates at the Sungai Sedu open dumping landfill during the dry season, characterize their spatial and temporal variations, and measure the CH₄ oxidation associated with the landfill cover soil using a homemade static flux chamber. Concentrations of the gases were analyzed by a Micro-GC CP-4900. Two methods, kriging values and inverse distance weighting (IDW), were found almost identical. The findings of the proposed method show that the ratio of CH₄ to CO₂ emissions was 25.4 %, indicating higher CO₂ emissions than CH₄ emissions. Also, the average CH₄ oxidation in the landfill cover soil was 52.5 %. The CH₄ and CO₂ emissions did not show fixed-pattern temporal variation based on daytime measurements. Statistically, a negative relationship was found between CH₄ emissions and oxidation (R ²?=?0.46). It can be concluded that the variation in the CH₄ oxidation was mainly attributed to the properties of the landfill cover soil.     

Road dust emissions from paved roads measured using different mobile systems

Very few real-world measurements of road dust suspension have been performed to date. This study compares two different techniques (referred to as Sniffer and Emma) to measure road dust emissions. The main differences between the systems are the construction of the inlet, different instruments for recording particulate matter (PM) levels, and different loads on the wheel axes (the weight of Sniffer was much higher than that of Emma). Both systems showed substantial small-scale variations of emission levels along the road, likely depending on-road surface conditions. The variations observed correlated quite well, and the discrepancies are likely a result of variations in dust load on the road surface perpendicular to the driving direction that cause variations in the measurements depending on slightly different paths driven by the two vehicles. Both systems showed a substantial influence on the emission levels depending on the type of tire used. The summer tire showed much lower suspension than the winter tires (one nonstudded and one studded). However, the relative importance of the nonstudded versus studded tire was rather different. For the ratio of studded/nonstudded, Emma shows higher values on all road sections compared with Sniffer. Both techniques showed increased emission levels with increasing vehicle speed. When the speed increased from 50 to 80 km hr(-1), the relative concentrations increased by 30-170% depending on the tire type and dust load. However, for road sections that were very dirty, Sniffer showed a much higher relative increase in the emission level with the nonstudded tire. Sniffer's absolute concentrations were mostly higher than Emma's. Possible reasons for the differences are discussed in the paper. Both systems can be used for studying relative road dust emissions and for designing air quality management strategies.     

Chemical absorption process for degradation of VOC gas using heterogeneous gas-liquid photocatalytic oxidation: toluene degradation by photo-Fenton reaction

A novel process for degradation of toluene in the gas-phase using heterogeneous gas-liquid photocatalytic oxidation has been developed. The degradation of toluene gas by photo-Fenton reaction in the liquid-phase has experimentally examined. The photo-Fenton reaction in the liquid-phase could improve the overall toluene absorption rate by increasing the driving force for mass transfer and as a result enhance the removal of toluene in the exhaust gas. The toluene concentrations in the inlet gas were varied in the range from 0.0968 to 8.69gm(-3) with initial hydrogen peroxide concentration of 400mgl(-1) and Fe dose of 5.0mgl(-1). It was found that toluene in the inlet gas was almost completely dissolved into water and degraded in the liquid-phase for the inlet toluene gas concentration of less than 0.42gm(-3). The dynamic process of toluene gas degradation by the photo-Fenton reaction providing information for reaction kinetics and mass transfer rate was examined. Toluene removal kinetic analysis indicated that photo-Fenton degradation was significantly affected by H(2)O(2) concentration. The experimental results were satisfactorily described by the predictions simulated using the simplified tanks-in-series model combined with toluene removal kinetic analysis. The present results showed that the proposed chemical absorption process using the photo-Fenton heterogeneous gas-liquid photocatalytic oxidation is very effective for degradation of volatile organic gases.     

Calibration Catchment Selection for Flood Regionalization Modeling1

Wan Jaafar, Wan Zurina, and Dawei Han, 2012. Calibration Catchment Selection for Flood Regionalization Modeling. Journal of the American Water Resources Association (JAWRA) 48(4): 698‐706. DOI: 10.1111/j.1752‐1688.2012.00648.x Abstract: There are two unsolved problems in flood regionalization model development related to the quantity and quality of calibration catchments: (1) how many calibration catchments should be used? and (2) how to select the calibration catchments? This study explores these two questions through a case study on the median annual maximum flood (QMED) model in the United Kingdom. It has been found that the chance of developing a good QMED model decreases significantly when the number of calibration catchments drops below a critical number (e.g., 60 in the case study). However, no significant improvement is achieved if the number of calibration catchments is above it. This number could be used as a benchmark for choosing randomly selected calibration catchments. Across a broad range of calibration catchment numbers, there are good and poor calibrated models regardless of calibration catchment numbers. High quality models could be developed from a small number of calibration catchments and also poor models from a large number of calibration catchments. This indicates that the number of calibration catchments may not be the dominating factor for developing a high quality regionalization model. Instead, the information content could be more important. The study has demonstrated that the standard deviation values between the best and poorest groups are distinctive and could be used in choosing appropriate calibration catchments.     

Selective metal leaching from technosols based on synthetic root exudate composition

This study focused on metal release from technosols induced by synthetic root exudate (SRE). The effect of SRE composition on metal release was studied using six technosols. This was done by treating the technosols with SRE solutions having varying concentrations of low molecular weight organic acids (LMWOAs), namely oxalic, citric, and malic acids. Consequently, the physico-chemical parameters (pH and electric conductivity), Ca, Mg, Fe, Zn, and Cu release (by atomic absorption spectroscopy, AAS), chemical changes (by Fourier transform infrared, FT-IR), and organic parameters (by fluorescence) were investigated. Metal release showed to be dependent on the SRE composition and technosol characteristics. Citric acid selectively released Ca, Mg, Zn, and Cu from technosols in a concentration-dependent manner; oxalic acid showed a significant role in the release of Mg and Fe. Under relatively high LMWOA concentrations, particulate organo-mineral complexes precipitated. Additionally, technosol weathering was seen by the dissolution of humic substances and ferriallophanes, which in turn caused metal release. However, re-precipitation of these phases showed to re-sorb metals, thus underestimating the role of LMWOAs in metal release. Therefore, the selective metal leaching was highly dependent on the SRE composition and LMWOA concentrations on one hand, and on the mineral, organic, and organo-mineral components of the technosols on the other. The understanding of such processes is crucial for proposing and implementing environmental management strategies to reduce metal leaching or for the beneficial re-usage of metals (e.g., for agromining) from technosols.     

Selenium and nano-selenium in plant nutrition

Selenium (Se) is a naturally occurring metalloid element which occurs nearly in all environments. Se is considered as a finite and non-renewable resource on the Earth. The common sources of Se in earth’s crust occur in association with sulfide minerals such as metal selenide, whereas it is rarely found in elemental form (Se⁰). While there is no evidence of Se need for higher plants, several reports show that when Se added at low concentrations, Se exerts beneficial effects on plant growth. Se may act as quasi-essential micronutrient through altering different physiological and biochemical traits. Thus, plants vary considerably in their physiological and biochemical response to Se. This review focusses on the physiological importance of Se forms as well as different Se fertilizers for higher plants, especially plant growth, uptake, transport, and metabolism.