Seasonal Variation of the Particle Size Distribution of n-Alkanes and Polycyclic Aromatic Hydrocarbons (PAHs) in Urban Aerosol of Guangzhou, China

Seasonal aerosol samples have been collected by Andersen Hi-Vol pumping system equipped with a five stage cascade impactor and a backup filter (size range: 10–7.2 μ m, 7.2–3.0 μ m, 3.0–1.5 μ m, 1.5–0.95 μ m, 0.95–0.49 μ m, ≤0.49 μ m) in the Liwan district, Guangzhou. n-Alkanes were measured using gas chromatography and PAHs were measured using gas chromatography/mass spectrometry analysis. The bimodal log-normal distributions of n-alkanes and semi-volatile PAHs were found, while for non-volatile PAHs that was unimodal, so much as the mode of semi-volatile PAHs was similar with that of the particles. The n-alkanes and PAHs were preferably associated with fine particles. C _max (carbon number maximum) (C₂₂–C₂₆), CPI (carbon preference index) (1.12–1.21), U/R (unresolved to resolved components ratio) (7.42–10.7), wax% (0.9–3.12%) and the diagnostic ratios for PAHs revealed that vehicular emission was the major source of these organic compounds during the study periods, while the contribution of epicuticular waxes emitted by terrestrial plants was minor. CPI₂ (values for petrogenic hydrocarbons), CPI₃ (values for biogenic n-alkanes) and wax% revealed that the natural preferentially accumulated in the larger aerosol while the anthropogenic in the smaller. In addition, the different MMDs (mass median diameters) for n-alkanes and PAHs were observed in different seasons. The MMDs for n-alkanes and PAHs were higher in autumn/winter than those in spring/summer. The seasonal effect was related to the hydrocarbon content in the individual particulate fractions, showing a preferential association of n-alkanes and PAHs with larger particles in the autumn/winter season.     

Extractable Hydrocarbons, Nickel and Vanadium Contents of Ogbodo-Isiokpo Oil Spill Polluted Soils in Niger Delta, Nigeria

An oil spill polluted site at Ogbodo-Isiokpo in Ikwere Local Government Area of Rivers State in southern Nigeria, was identified for study following three successive reconnaissance surveys of oil fields in the Agbada west plain of Eastern Niger Delta. A sampling area of 200 m × 200 m was delimited at the oil spill impacted site using the grid technique and soils were collected at surface (0–15 cm) and subsurface (15–30 cm) depths from three replicate quadrats. A geographically similar, unaffected area, located 50 m adjacent to the polluted site, was chosen as a control (reference) site. Total extractable hydrocarbon contents of the polluted soils ranged from 3.02–4.54 and 1.60–4.20 mg/kg (no overlap in standard errors) at surface and subsurface depths respectively. The concentrations of two “diagnostic” trace heavy metals, nickel (Ni) and vanadium (V), which are normal constituents of crude oil, were also determined in the soils by atomic absorption spectrophotometric method after pre-extraction of cations with dithionite–citrate carbonate. Ni varied from 0.15 to 1.65 mg/kg in the polluted plots and from 0.18 to 0.82 mg/kg in the unpolluted plots; vanadium varied from 0.19 to 0.70 mg/kg in the polluted plots and from 0.14 to 0.38 mg/kg in the unpolluted plots. Ni and V were more enhanced (p < 0.05) in the oil-polluted soils, especially at subsurface depth. Whilst the oil spillage could be said to be indirectly responsible for the enhanced concentrations of nickel and vanadium via the injection and availability of the petroleum hydrocarbons that might have increased the activities of biodegradation on site, the physico-chemical properties of the soils and inherent mobility of metals, as well as the intense rainfall and flooding that characterized the period of study, may have also contributed, at least in part, to these enhanced concentrations. Such levels of Ni and V may result to enhanced absorption by plants, which may bring about possible bioaccumulation in such plants and the animals that depend on them for survival and all of these may lead to toxic reactions along the food chain.     

Implications of climate change for evaporation from bare soils in a Mediterranean environment

The purpose of this study was to predict quantitative changes in evaporation from bare soils in the Mediterranean climate region of Turkey in response to the projections of a regional climate model developed in Japan (hereafter RCM). Daily RCM data for the estimation of reference evapotranspiration (ET _r) and soil evaporation were obtained for the periods of 1994–2003 and 2070–2079. Potential evaporation (E _p) from bare soils was calculated using the Penman–Monteith equation with a surface resistance of zero. Simulation of actual soil evaporation (E _a) was carried out using Aydin model (Aydin et al., Ecological Modelling 182:91–105, 2005) combined with Aydin and Uygur (2006, A model for estimating soil water potential of bare fields. In Proceedings of the 18th International Soil Meeting (ISM) on Soils Sustaining Life on Earth, Managing Soil and Technology, Sanliurfa, 477–480pp.) model of predicting soil water potential at the top surface layer of a bare soil, after performances of Aydin model (R ² = 94.0%) and Aydin and Uygur model (R ² = 97.6) were tested. The latter model is based on the relations among potential soil evaporation, hydraulic diffusivity, and soil wetness, with some simplified assumptions. Input parameters of the model are simple and easily obtainable such as climatic parameters used to compute the potential soil evaporation, average diffusivity for the drying soil, and volumetric water content at field capacity. The combination of Aydin and Aydin and Uygur models appeared to be useful in estimating water potential of soils and E _a from bare soils, with only a few parameters. Unlike ET _r and E _p projected to increase by 92 and 69 mm (equivalent to 8.0 and 7.3% increases) due to the elevated evaporative demand of the atmosphere, respectively, E _a from bare soils is projected to reduce by 50 mm (equivalent to a 16.5% decrease) in response to a decrease in rainfall by 46% in the Mediterranean region of Turkey by the 2070s predicted by RCM, and consequently, to decreased soil wetness in the future.     

Gas chromatographic fingerprinting of crude oil from Idu-Ekpeye oil spillage site in Niger-delta, Nigeria

Samples were collected from an oil polluted site in Niger-delta, Nigeria. Gas chromatographic analyses carried out on the samples revealed an abundance of n-alkanes within the n-C₈–n-C₂₃ region. The pristane/phytane ratio of 5.70 obtained for the samples depicted a plant/terrestrial source input and a possible oxic depositional environment. The n-C₁₇/pristane and n-C₁₈/phytane ratios of 2.80 and 2.77, respectively, suggested that the spilled oil was only slightly weathered, as corroborated by the presence of peaks in the aromatic hydrocarbon fingerprints. The polycyclic aromatic hydrocarbon (PAH) fractions showed that the hydrocarbon fractions might have undergone combustion and/or that there was bush burning at the site prior to the oil spill incidence. This is supported by the abundance of high-molecular-weight PAHs which are pyrogenic in nature. High molecular weight PAHs are products of the combustion of petroleum or its products. The phenanthrene/anthracene ratio of 0.95, fluorathene/pyrene ratio of 2.23 and the ∑ (other three to six ringed PAHs)/∑ (five alkylated PAHs) ratio far greater than unity (4.10) also affirm this. On the other hand, the benzo (a) anthracene to chrysene ratio of 0.24 confirms the petrogenic origin of the spilled oil because chrysene which is highly abundant is a fossil PAH.     

Long-term variability of metals from fungicides applied in amended young vineyard fields of La Rioja (Spain)

The long-term variability of total Cu content from fungicides applied in a certified wine region of Spain (La Rioja) and of other metals (Cd, Cr, Ni, Pb, and Zn) was evaluated in three young vineyard soils and subsoils unamended and amended with spent mushroom substrates (SMS) over a 3-year period (2006–2008). SMS is a promising agricultural residue as an amendment to increase the soil organic matter content but may modify the behaviour of metals from pesticide utilisation in vineyards. Fresh and composted SMS was applied each year at a rate of 25 t ha⁻¹ (dry-weight). Copper concentrations in the three unamended soils were 21.2–88.5, 25.5–77.1, and 29.4–78.4 mg kg⁻¹. They exceeded natural Cu concentrations of the region and reference sub-lethal hazardous concentration for soil organism. The concentrations of Cd, Ni, Pb, and Zn were largely below the sub-lethal limits. Thus, although Cu levels were lower than those of established vineyards, vine performance, and productivity might be affected. The variation in behaviour between different amendments for each soil was high, so a generic conclusion could not be drawn. The amendment practice seemed to have caused temporarily Cu mobilization respect to untreated soils. Total zinc concentrations fall within the range of the natural soil of La Rioja and were significantly affected (p < 0.05) especially by fresh state SMS addition, with increasing up to 75% respect to untreated specimen. The results indicated a build-up of fresh sites for metal retention at both surface and subsurface level, although no accumulation of metals was observed in the short-term period. However, the benefit for soils and the negative effects need to be monitored in the long run.     

Spatial and seasonal distribution of nitrogen in marsh soils of a typical floodplain wetland in Northeast China

Horizontal and profile distributions of nitrogen in marsh soils in different seasons were studied in a typical site within the Erbaifangzi wetland in Northeast China. Results showed that there was higher spatial heterogeneity for nitrate nitrogen (NO₃^--_{3}^{-}-N) and ammonium nitrogen (NH₄⁺_{4}^{+}–N), as well as available nitrogen (AN), in surface soils in July compared to that in September. Relative to July, the mean nitrogen contents in surface soils were slightly higher in September; however, in November, soils contained significantly lower NO₃^--_{3}^{-}-N and NH₄⁺_{4}^{+}–N, higher AN, organic nitrogen (Org-N), and total nitrogen (TN). Except for mineral nitrogen, no significant differences were observed between Org-N and TN contents in September and November. Nitrogen contents generally declined exponentially with depth along soil profiles in three sampling dates (July, September, and November), except for a significant accumulation peak of NO₃^--_{3}^{-}-N at the 20–30 cm depth in September. However, NH₄⁺_{4}^{+}–N contents showed a vertical alternation of “increasing and decreasing” in both July and September, while nearly kept constant with depth in November. The depth ranking of nitrogen showed the shallowest distribution for AN, followed by Org-N and TN, while deeper distributions for NO₃^--_{3}^{-}-N and NH₄⁺_{4}^{+}–N. TN, Org-N, and AN were significantly correlated with soil organic matter and total phosphorus. Soil pH values were significantly correlated with TN and AN contents in surface soils. Clay contents showed significant correlations with nitrogen contents except for NO₃^--_{3}^{-}-N in surface soils and NH₄⁺_{4}^{+}–N in profile soils. However, soil moisture was not significantly correlated with nitrogen contents among all soil samples.     

Heavy metals and PCDD/Fs in solid waste incinerator fly ash in Zhejiang province,China: chemical and bio-analytical characterization

Fly ash samples were taken from solid waste incinerators with different feeding waste, furnace type, and air pollution control device in six cities of Zhejiang province. The solid waste incinerators there constitute one fifth of incinerators in China. Heavy metals and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were analyzed in the fly ash. Moreover, the fly ash samples were extracted by toxicity characteristic leaching procedure (TCLP). The biotoxicity of the leachate was evaluated by Chlorella pyrenoidosa. High variation and contents were found for both the heavy metals and PCDD/Fs. The contents of Zn, Cu, As, Pb, Cd, Cr, Ni, and Hg in the fly ash samples varied from 300 to 32,100, 62.1–1175, 1.1–57, 61.6–620, 0.4–223, 16.6–4380, 1.2–94.7, and 0.03–1.4 μg g⁻¹ dw, respectively. The total contents of 17 PCDD/Fs varied from 0.1128 to 127.7939 μg g⁻¹ dw, and the 2,3,7,8-TeCDD toxic equivalents (TEQ) of PCDD/Fs ranged from 0.009 to 6.177 μg g⁻¹ dw. PCDF congeners were the main contributor to the TEQ. The leachate of the fly ash showed biotoxicity to C. pyrenoidosa. A significant correlation was found between the Cd and EC₅₀ values. Further research is required to investigate the environmental impact of the various pollutants in the fly ash.     

Application of a Larval Medaka Assay to Evaluate the Fish Safety Level in Sagami River, Japan

Physico-chemical characteristics of some river and hand-dug well waters used for drinking and domestic purposes in the oil rich Niger Delta area of Nigeria were assessed using standard methods. The concentrations of the parameters in the river water samples ranged in the following order: pH (5.6–6.9), temperature (26.90–28.60°C), turbidity (23–63 NTU), electrical conductivity (52–184 μs/cm), DO (5.4–7.2 mg/l), BOD (21–57 mg/l), TDS (6.0–217 mg/l), PO₄ ³⁻ (0.19–1.72 mg/l), SO₄ ²⁻ (25–36.8 mg/l), NO₃ ⁻ (20.3–28 mg/l), Fe (6.07–15.71 mg/l), Zn (0.04–0.24 mg/l), Pb (0.01–0.17 mg/l), Ni (0.01–0.13 mg/l), Vn (0.01–0.20 mg/l) and Hg (0.001–0.002 mg/l). The concentrations of these parameters in the hand-dug well water ranged in the following order: pH (5.7–6.8) temperature (26–30°C), turbidity (134–171 NTU), electrical conductivity (160–340 μs/cm), DO (5.4–6.4 mg/l), BOD (13–34 mg/l), TDS (110–190 mg/l), PO₄ ³⁻ (0.84–1.84 mg/l), SO₄ ²⁻ (10.6–28.1 mg/l), NO₃ ⁻ (11.3–23 mg/l), Fe (13.17–16.31 mg/l), Ni (0.01–0.02 mg/l), Vn (0.01–0.04 mg/l) and Hg (0.001–0.004 mg/l). The concentrations of BOD, turbidity, NO₃ ⁻ and Fe in the water samples were above WHO and FMENV permissible limits for safe drinking water. The results suggest that the use of such waters for drinking and domestic purposes pose a serious threat to the health of the users and calls for the intervention of government agencies.     

Desorption Kinetics of Benzene in a Sandy Soil in the Presence of Powdered Activated Carbon

Desorption kinetics of benzene was investigated with a modified biphasic desorption model in a sandy soil with five different powdered activated carbon (PAC) contents (0, 1, 2, 5, 10% w/w) as sorbents. Sorption experiments followed by series dilution desorption were conducted for each sorbent. Desorption of benzene was successively performed at two stages using deionized water and hexane. Modeling was performed on both desorption isotherm and desorption rate for water-induced desorption to elucidate the presence of sorption–desorption hysteresis and biphasic desorption and if present to quantify the desorption-resistant fraction (q _irr) and labile fraction (F) of desorption site responsible for rapid process. Desorption isotherms revealed that sorption–desorption exhibited a severe hysteresis with a significant fraction of benzene being irreversibly adsorbed onto both pure sand and PAC, and that desorption-resistant fraction (q _irr) increased with PAC content. Desorption kinetic modeling showed that desorption of benzene was biphasic with much higher (4–40 times) rate constant for rapid process (k ₁) than that for slow process (k ₂), and that the difference in the rate constant increased with PAC content. The labile fraction (F) of desorption site showed a decreasing tendency with PAC. The experimental results would provide valuable information on remediation methods for soils and groundwater contaminated with BTEX.     

Heavy Metal and Trace Elements in Various Fish Samples from Sır Dam Lake, Kahramanmaraş, Turkey

Achanthobrama marmid (thorn-bream) (n:24), Chondrostoma regium (nose-carp) (n:33) and Silurus glanis (wels) (n:21), and Cyprinus carpio (carp) (n:30) were collected from Sır Dam Lake in Kahramanmaraş Province. The iron (Fe), manganese (Mn), cobalt (Co), nickel (Ni), and lead (Pb) levels were determined in the total of 108 fish samples by Atomic Absorption Spectrophotometer. The concentrations of heavy metals were expressed as mg kg⁻¹ wet weight of tissue. The mean Fe and Mn levels of muscle and gill of C. carpio were 0.8–5.71 and 0.30–1.96, respectively. The mean of the Fe and Mn levels of muscle and gill of A. marmid were 1.22, 5.07 and 0.38, 0.85 mg kg⁻¹, respectively. The ranges of mean concentrations of Fe and Mn levels in muscle and gill of C. regium were 0.91, 5.61 and 0.27, 3.42 mg kg⁻¹, respectively. The mean value of Fe in S. glanis gill was 1.03, which of Mn was 0.17 mg kg⁻¹. Fe, Mn, Co, Ni, and Pb were not detected in the muscle of S. glanis. The mean values for Co in muscle of thorn-bream, carp, and nose-carp were 0.005, 0.01, 0.0 mg kg⁻¹, respectively. Nickel values in the muscle were ranged between 0.38 and 1.93 in thorn-bream, 0.06 and 1.34 in carp, 0.14 and 1.89 in nose-carp, in that order. The mean Pb levels of muscle and gill of A. marmid were 0.14 and 0.29 mg kg⁻¹, respectively. The mean values of Pb concentration of muscle and gill for C. carpio were 0.13 and 0.50 mg kg⁻¹, respectively. In C. regium mean values for Pb in muscle and gill were 0.06 and 0.06 mg kg⁻¹, respectively. The mean value of Pb in S. glanis gill was 0.42, ranged between 0.0–0.92 mg kg⁻¹.     

Element contents and food safety of water spinach (Ipomoea aquatica Forssk.) cultivated with wastewater in Hanoi, Vietnam

Extensive aquatic or semi-aquatic production of water spinach (Ipomoea aquatica Forssk.) for human consumption takes place in Southeast Asia. The aim of this study was to assess the concentrations of 38 elements in soil and water spinach cultivated under different degrees of wastewater exposure in Hanoi, Vietnam. The results showed no effect of wastewater use on the overall element concentrations in soil and water spinach. Mean soil concentrations for selected potentially toxic elements at the studied field sites had the following ranges 9.11–18.7 As, 0.333–0.667 Cd, 10.8–14.5 Co, 68–122 Cr, 34.0–62.1 Cu, 29.9–52.8 Ni, 32.5–67.4 Pb, 0.578–0.765 Tl and 99–189 Zn mg kg⁻¹ dry weight (d.w.). In all samples Cd, Pb and Zn soil concentrations were below the Vietnamese Guideline Values (TCVN 7209-2002) for agricultural soils whereas As and Cu exceeded the guideline values. Maximum site element concentrations in water spinach were 0.139 As, 0.032 Cd, 0.135 Cr, 2.01 Cu, 39.1 Fe, 57.3 Mn, 0.16 Ni, 0.189 Pb and 6.01 Zn mg kg⁻¹ fresh weight (f.w.). The site and soil content of organic carbon were found to have high influence on the water spinach element concentrations whereas soil pH and the total soil element concentrations were of less importance. The estimated average daily intake of As, Cd, Cu, Fe, Pb and Zn for adult Vietnamese consumers amounts to <11% of the maximum tolerable intake proposed by FAO/WHO for each element. It is assessed that the occurrence of the investigated elements in water spinach will pose low health risk for the consumers.     

Irrigation Efficiency and Quality of Irrigation Return Flows in the Ebro River Basin: An Overview

The review analysis of twenty two irrigation efficiency (IE) studies carried out in the Ebro River Basin shows that IE is low (average IE)_avg(= 53%) in surface-irrigated areas with high-permeable and shallow soils inadequate for this irrigation system, high (IE)_avg(= 79%) in surface-irrigated areas with appropriate soils for this system, and very high (IE)_avg(= 94%) in modern, automated and well managed sprinkler-irrigated areas. The unitary salt (total dissolved solids) and nitrate loads exported in the irrigation return flows (IRF) of seven districts vary, depending on soil salinity and on irrigation and N fertilization management, between 3–16 Mg salt/ha⋅ year and 23–195 kg NO)₃ ⁻-N/ha⋅ year, respectively. The lower nitrate loads exported from high IE districts show that a proper irrigation design and management is a key factor to reduce off-site nitrogen pollution. Although high IE’s also reduce off-site salt pollution, the presence of salts in the soil or subsoil may induce relatively high salt loads (≥14 Mg/ha⋅ year) even in high IE districts. Two important constrains identified in our revision were the short duration of most surveys and the lack of standards for conducting irrigation efficiency and mass balance studies at the irrigation district level. These limitations {emphasize the need for the establishment of a permanent and standardized network of drainage monitoring stations for the appropriate off-site pollution diagnosis and control of irrigated agriculture.     

Hydrogen Peroxide and Ultraviolet Irradiations in Water Treatment

Trihalomethanes (THMs) the by-products of chlorination in water treatment are recognised as a threat to public health due to their carcinogenicity. The photodegradation of THMs using hydrogen peroxide has been found to give increased removal efficiency and the outcome of the study may find, its application in designing a unit process for water treatment. Batch experiments were carried out using UV lamp of 83 W and 40% w/w Hydrogen peroxide (H₂O₂) in test waters between 2.5–10 pH range of chloroform, bromodichloromethane, dibromochloromethane and bromoform at 50–200 μg L⁻¹ initial concentration. 92–100% removal of chloroform, bromodichloromethane, dibromochloromethane and bromoform were found with 0.1% of H₂O₂ and 90 min of UV exposure.     

Water quality assessment: surface water sources used for drinking and irrigation in Zaria,Nigeria are a public health hazard

We assessed the quality and pollution status of source surface waters in Zaria, Nigeria by monitoring the nature, cause and extent of pollution in Samaru stream, Kubanni River and Kubanni dam over a period of 10 months, between March and December 2002. A total of 228 water samples was collected from 12 sites and analysed for a total of ten physicochemical and one bacteriological quality indicators, using standard methods. Aesthetic water quality impairment parameters were also observed. The mean values of most water quality parameters were significantly higher (P < 0.05) in both the stream and river than in the dam. There was no significant correlation between faecal coliform counts (FCC) and water temperature (in the range 15–33°C); pH (5.77–7.32); and turbidity (1.4–567 NTU). The high FCC ranged from 2.0 × 10¹ to 1.6 × 10⁶ MPN/100 ml and exceeded the WHO standards for drinking water and water used for fresh-produce irrigation, and correlated positively (P < 0.05) with conductivity (in the range 68–1,029 μS/cm); TDS (10.0–70.0 mg/l); TSS (10.0–70.0 mg/l); Cl (7.5–181 mg/l); PO₄⁻P (0.01–0.41 mg/l); NO₃⁻N (0.6–3.8 mg/l) and BOD₅ (0.1–14.9 mg/l). The main pollution sources were municipal wastewater, stormwater runoffs, the ABU sewage treatment plant, abattoir effluents and irrigation farms treated with chemical fertilisers. We conclude that these water bodies are potentially hazardous to public health and that proper sewage treatment and river quality monitoring are needed to warn against hazards to public health.     

Cyanobacterial Flora from Polluted Marine Shores

Citation of cyanobacterial cultures from the shores of south west coast of Gujarat, India and their relationship with sea water quality, influenced by extensive pollutant runoff is reported in this study. Intensity of pollution was evaluated by physico-chemical analysis of water. Higher load of suspended solids (60–1000 mg l⁻¹) and nutrients (PO₄ ⁻P: 1.3–4 μmole l⁻¹ and NO₃ ⁻N: 12.5–17.8 μmole l⁻¹) were persistent throughout the analysis. Community structure is seen to be influenced by such persistent pollution. Twenty nine cyanobacterial species were isolated belonging to 9 genera of 4 families, with an elevated occurrence of Oscillatoria and Lyngbya species. No heterocystous cyanobacteria were isolated throughout the study.     

Trace Metal Levels in Mussels (Mytilus Galloprovincialis L. 1758) from Turkish Aegean Sea Coast

Bio-monitoring of some heavy metal levels (Cd, Pb, Zn, Cu) in whole edible soft parts of Mytilus galloprovincialis (L. 1758) was conducted in Turkish Aegean Sea coast during the period of September 2002–August 2003 seasonally. Moreover, some physico-chemical environmental parameters, also have been analysed in the same region. The values of some physico-chemical environmental parameters in coastal waters of Turkish Aegean Sea were changed between; 9.0–27.0 ^∘C for temperature, 31.93–40.45 psu for salinity, 7.35–8.48 for pH and 4.05–9.50 mg/l for dissolved oxygen. The levels of trace elements in whole edible soft parts including interstitial fluids of Mediterranean mussels M. galloprovincialis (L. 1758), sampled from 6 different regions of Turkish Aegean Sea coast have ranged between; 0.04–0.52 μg Cd/g wet weight, 0.49–1.72 μg Pb/g w.w., 0.95–1.85 Cu/g w.w., 16.11–37.15 μg Zn/g w.w. The highest values for all trace metals (Cd, Pb, Zn, Cu) were measured in inner part of Izmir Bay (station 3) and lowest in Sigacik and Gulluk Bay (station 5, 6). Generally heavy metal levels are lower than the results in soft mussel tissues reported from Mediterranean regions.     

Comparison of some quality properties of soils around land-mined areas and adjacent agricultural fields

When agricultural lands are no longer used for agriculture and allowed to recover its natural vegetation, soil organic carbon can accumulate in the soil. Measurements of soil organic carbon and aggregate stability changes under various forms of land use are needed for the development of sustainable systems. Therefore, comparison of soil samples taken from both agricultural and nearby area close to land-mined fields where no agricultural practices have been done since 1956 can be a good approach to evaluate the effects of tillage and agriculture on soil quality. The objective of this study was to compare tillage, cropping and no tillage effects on some soil-quality parameters. Four different locations along the Turkey–Syria border were selected to determine effects of tillage and cropping on soil quality. Each location was evaluated separately because of different soil type and treatments. Comparisons were made between non-tilled and non-cropped fallow since 1956 and adjacent restricted lands that were tilled about every 2 years but not planted (T) or adjacent lands tilled and planted with wheat and lentil (P). Three samples were taken from the depths of 0–20 and 20–40 cm each site. Soil organic carbon (SOC), pH ,electrical conductivity, water soluble Ca⁺⁺, Mg⁺⁺, CO₃^-2{\rm CO}_{3}^{-2} and HCO₃^-{\rm HCO}_{3}^{-}, extractable potassium (K⁺) and sodium (Na⁺), soil texture, ammonium (NH₄⁺{\rm NH}_{4}^{+}–N) and nitrate (NO₃–N), extractable phosphorous and soil aggregate stability were determined. While the SOC contents of continuous tillage without cropping and continuous tillage and cropping were 2.2 and 11.6 g kg⁻¹, respectively, it was 30 g kg⁻¹ in non-tilled and non-planted site. Tillage of soil without the input of any plant material resulted in loss of carbon from the soil in all sites. Soil extractable NO₃−N contents of non-tilled and non-cropped sites were greatest among all treatments. Agricultural practices increased phosphorus and potassium contents in the soil profile. P₂O₅ contents of planted soils were approximately 20 to 39 times greater than those of non-tilled and non-cropped soils at different sites. FTIR spectra showed that never tilled sites had greater phenol, carboxylic acid, amide, aromatic compounds, polysaccharide and carbohydrates than other treatments.     

Facile and Sensitive Spectrophotometric Determination of Carbosulfan in Formulations and Environmental Samples

Facile, selective and sensitive spectrophotometric method has been developed for the determination of carbosulfan in insecticidal formulations, fortified water, food grains, agriculture wastewater and soil samples with newly synthesized reagents. The method was based on acid and alkaline hydrolysis of the carbosulfan pesticide, and the resultant hydrolysis product of carbosulfan was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λ _max of 464 nm or interaction with 2,6-dibromo-4-nitroaniline to produce yellow colored product with λ _max of 408 nm or coupling with 2,4,6-tribromoaniline to form red colored product has a λ _max of 471 nm. Under optimal conditions, Beer’s law range for 2,6-dibromo-4-methylaniline (DBMA) was found to be 0.2–12.0 μg ml⁻¹, 0.6–16.0 μg ml⁻¹ for 2,6-dibromo-4-nitroaniline (DBNA) and 0.4–15.0 μg ml⁻¹ for 2,4,6-tribromoaniline (TBA). The molar absorptivity of the color systems were found to be 3.112 × 10⁴ l mol⁻¹ cm⁻¹ for DBMA, 3.214 × 10⁴ l mol⁻¹ cm⁻¹ for DBNA and 3.881 × 10⁴ l mol⁻¹ cm⁻¹ for TBA. Sandell’s of the color reactions are 0.013 μg cm⁻² (DBMA), 0.012 μg cm⁻² (DBNA) and 0.011 μg cm⁻² (TBA) respectively. The effect of the non-target species on the determination of carbosulfan was studied to enhance the selectivity of the proposed methods. The formation of colored derivatives with the coupling agents is instantaneous and stable for 28, 30, and 26 h. Performance of the proposed methods were compared statistically in terms Student’s F and t-tests with the reported methods. An erratum to this article can be found at     

Aerosol characteristics and surface radiative forcing components during a dust outbreak in Gwangju, Republic of Korea

Atmospheric surface aerosol radiative forcing (SARF) ΔF, forcing efficiency ΔF_e and fractional forcing efficiency ΔFF_e evaluated from cloud-screened narrowband spectral and thermal-offset-corrected radiometric observations during the Asia dust outbreak episodes in Gwangju, Republic of Korea are reported in this study. Columnar aerosol optical properties (aerosol optical depth (AOD), τ _aλ, Angstrom exponent α, mass concentration of fine and coarse mode particles) were also reported for the station between January 2000 and May 2001 consisting of 211cloud-free days. Results indicate that majority of the AOD were within the range 0.25–0.45 while some high aerosol events in which AODs ≥ 0.6 were observed during the severe dust episodes. For example, AOD increases from annual average value of 0.34 ± 0.13 at 501 nm to values >0.60 during the major dust events of March 27–30 and April 7–9, 2000, respectively. The α _{501–870 nm} which is often used as a qualitative indicator of aerosol particle size had values ranging from 0.01 to 1.77. The diurnal forcing efficiency ΔDF_e at Gwangju was estimated to be −81.10 ± 5.14 W m ⁻²/τ _{501 nm} and −47.09 ± 2.20 W m ⁻²/τ _{501 nm} for the total solar broadband and visible band pass, respectively while the fractional diurnal forcing efficiency ΔFDF_e were −15.8 ± 0.64%/τ _{501 nm} and −22.87 ± 1.13%/τ _{501 nm} for the same band passes. Analyses of the 5-day air-mass back trajectories were further developed for Gwangju in order to classify the air-mass and types of aerosol reaching the site during the Asia dust episodes.     

Distribution of heavy metals in the dissolved and suspended phase of the sea-surface microlayer, seawater column and in sediments of Singapore’s coastal environment

Concentrations of heavy metals were determined in the water column (including the sea-surface microlayer, subsurface, mid-depth and bottom water) and sediments from Singapore’s coastal environment. The concentration ranges for As, Cd, Cr, Cu, Ni, Pb and Zn in the seawater dissolved phase (DP) were 0.34–2.04, 0.013–0.109, 0.07–0.35, 0.23–1.16, 0.28–0.78, 0.009–0.062 and 0.97–3.66 μg L⁻¹ respectively. The ranges for Cd, Cr, Cu, Ni, Pb and Zn in the suspended particulate matter (SPM) were 0.16–0.73, 6.72–53.93, 12.87–118.29, 4.34–60.71, 1.10–6.08 and 43.09–370.49 μg g⁻¹, respectively. Heavy metal concentrations in sediments ranged between 0.054–0.217, 37.48–50.52, 6.30–21.01, 13.27–26.59, 24.14–37.28 and 48.20–62.36 μg g⁻¹ for Cd, Cr, Cu, Ni, Pb and Zn, respectively. The lowest concentrations of metals in the DP and SPM were most frequently found in the subsurface water while the highest concentrations were mostly observed in the SML and bottom water. Overall, heavy metals in both the dissolved and particulate fractions have depth profiles that show a decreasing trend of concentrations from the subsurface to the bottom water, indicating that the prevalence of metals is linked to the marine biological cycle. In comparison to data from Greece, Malaysia and USA, the levels of metals in the DP are considered to be low in Singapore. Higher concentrations of particulate metals were reported for the Northern Adriatic Sea and the Rhine/Meuse estuary in the Netherlands compared to values reported in this study. The marine sediments in Singapore are not heavily contaminated when compared to metal levels in marine sediments from other countries such as Thailand, Japan, Korea, Spain and China.