Chemical characteristics of groundwater in parts of mountainous region, Alvand, Hamadan, Iran

Eighty-seven groundwater samples have been collected from a mountainous region (Alvand, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. Most water quality parameters are within World Health Organization acceptable limits set for drinking water. The least mineralized water is found closest to the main recharge zones and the salinity of water increased towards the north of the basin. The most prevalent water type is Ca–HCO₃ followed by water types Ca–NO₃, Ca–Cl, Ca–SO₄ and Mg–HCO₃. The Ca–NO₃ water type is associated with high nitrate pollution. Agricultural and industrial activities were associated with elevated level of NO₃⁻. Mineral dissolution/weathering of evaporites dominates the major element hydrochemistry of the area. Chemical properties of groundwater in Alvand region are controlled both by natural geochemical processes and anthropogenic activities.     

Nitrate pollution of groundwater in Toyserkan,western Iran

A total of 95 groundwater samples were collected from Toyserkan, western Iran to assess the chemical composition and nitrate (NO₃ ⁻) status of groundwater. The most prevalent water type is Ca–HCO₃ followed by water types Ca–Mg–HCO₃. In comparison with the World Health Organization (WHO) drinking water guideline of 50 mg l⁻¹ for NO₃ ⁻, a total of nine wells (9.5%) showed higher concentrations. In 36% of samples (34) NO₃ ⁻ concentration was low (<20 mg l⁻¹), and in 53.7% of samples (51), in the range of 20–50 mg l⁻¹. The samples were classified into four groups based on NO₃ ⁻ and chloride (Cl⁻) concentrations. Of the samples, 40% were classified as group 4 and were relatively high in Cl⁻ and NO₃ ⁻ (Cl⁻ > 47 mg l⁻¹, NO₃ ⁻ > 27 mg l⁻¹). The high correlation between NO₃ ⁻ and Cl⁻ (r = 0.86, p < 0.01) is consistent with a manure source, resulting from the practice of adding salt to animal feed. Pollution of groundwaters appeared to be affected by the application of inorganic fertilizer at greater than agronomic rates, Cl-salt inputs, and irrigation practice.     

Effect of water quality on the leaching of potassium from sandy soil

When potassium (K⁺) fertilizers are applied to soil, K⁺ is subject to displacement through the soil profile. More generally, the application of K⁺ fertilizers to sandy soils with low clay content and small buffer capacity, in which K⁺ does not interact strongly with the soil matrix, results in localized increases in K⁺ concentration in the soil solution. Losses of K⁺ depend on the concentration of calcium (Ca²⁺) as a competing ion in the leaching water and the amount of water that passes through the soil. In this study, we examined the adsorption and movement of applied K⁺ in columns of sandy soil. Glass tubes, 4.8 cm in diameter and 40 cm in length, were packed with either native soil or Ca²⁺-saturated soil. The resulting 10-cm-long column of soil had a bulk density of 1.65 g cm⁻³. Native soil was leached with distilled water and CaCl₂ solutions of various concentrations. In the Ca²⁺-saturated soil, a pulse of K⁺ was leached with CaCl₂ solutions of various concentrations or distilled water. Increasing the CaCl₂ concentration from 3 to 15 mm resulted in earlier breakthrough, a higher peak concentration of K⁺, and greater amounts of leached K⁺. The breakthrough curve for K⁺, when leached with distilled water, showed very low concentrations and was more delayed than the other treatments. In Ca²⁺-saturated soil, the amount of K⁺ leached increased as Ca²⁺ concentration increased, with up to 54% of the added pulse K⁺ being removed from 10 pore volumes (Pv) (387 mm) of 15 mm CaCl₂. The presence of Ca²⁺ in irrigation water and soil minerals able to release Ca²⁺ is important in determining the amount of K⁺ leached from soils. Large amounts of K⁺ are leached from soils in areas where crops are irrigated with water that contains significant concentrations of Ca²⁺ and other cations.     

The interaction of two asymmetric quasi-geostrophic vortex patches

ABSTRACT

Herein we study the general interaction of two vortex patches in a single-layer quasi-geostrophic shallow-water flow. Steadily-rotating equilibrium states are found over a wide parameter space spanning the Rossby deformation length, vortex area ratio, potential vorticity ratio, and gap between their innermost edges. A linear stability analysis is then used to identify the critical gap separating stable and unstable solutions, over the entire range of area and potential vorticity ratios, and for selected values of the Rossby deformation length. A representative set of marginally unstable equilibrium states are then slightly perturbed and evolved by an accurate contour dynamics numerical algorithm to understand the long-term fate of the instabilities. Not all instabilities lead to vortex merger; many in fact are characterised by weak filamentation and a small adjustment of the vortex shapes, without merger. Stronger instabilities lead to material being torn from one vortex and either wrapped around the other or reduced to ever thinning filamentary debris. A portion of the vortex may survive, or it may be completely strained out by the other.     

Hydrogeochemistry of Groundwater and Its Suitability for Drinking and Agricultural Use in Nahavand,Western Iran

Groundwater is the major source of drinking water in Nahavand city. However, the groundwater quality at the agricultural areas has been deteriorating in recent years. Ground water quality monitoring is a tool which provides important information for water management and sustainable development of the water resources in Nahavand. Hydrochemical investigations were carried out in an agricultural area in Nahavand, western Iran, to assess chemical composition of groundwater. In this study, 64 representative groundwater samples were collected from different irrigation wells and analyzed for pH, electrical conductivity, major ions, and nitrate. The results of the chemical analysis of the groundwater showed that concentrations of ions vary widely and the most prevalent water type is Ca–Mg–HCO₃, followed by other water types: Ca–HCO₃, Ca–Na–HCO₃, and Na–Cl, which is in relation with their interactions with the geological formations of the basin, dissolution of feldspars and chloride and bicarbonate minerals, and anthropogenic activities. Thirty-seven percent of the water samples showed nitrate (NO₃ ⁻) concentrations above the human affected value (13 mg L⁻¹). The phosphorous (P) concentration in groundwater was between 0.11 and 0.90 mg L⁻¹, with an average value of 0.30 mg L⁻¹, with all of the samples over 0.05 mg L⁻¹. The most dominant class C2-S1 (76.5%) was found in the studied area, indicating that sodicity is very low and salinity is medium, and that these waters are suitable for irrigation in almost all soils. Agronomic practices, such as cultivation, cropping, and irrigation water management may decrease the average NO₃ ⁻ concentration in water draining from the soil zone.     

Environmental contamination of Zn,Cd, Ni,Cu, and Pb from industrial areas in Hamadan Province,western Iran

Eleven surface soil samples from calcareous soils of industrial areas in Hamadan Province, western Iran were analyzed for total concentrations of Zn, Cd, Ni, Cu and Pb and were sequentially extracted into six fractions to determine the bioavailability of various heavy metal forms. Total Zn, Cd, Ni, Cu and Pb concentrations of the contaminated soils were 658 (57–5,803), 125.8 (1.18–1,361), 45.6 (30.7–64.4), 29.7 (11.7–83.5) and 2,419 (66–24,850) mg kg⁻¹, respectively. The soils were polluted with Zn, Pb, and Cu to some extent and heavily polluted with Cd. Nickel values were not above regulatory limits. Copper existed in soil mainly in residual (RES) and organic (OM) fractions (about 42 and 33%, respectively), whereas Zn occurred essentially as RES fraction (about 69%). The considerable presence of Cd (30.8%) and Pb (39%) in the CARB fraction suggests these elements have high potential biavailability and leachability in soils from contaminated soils. The mobile and bioavailable (EXCH and CARB) fractions of Zn, Cd, Ni, Cu, and Pb in contaminated soils averaged (7.3, 40.4, 16, 12.9 and 40.8%), respectively, which suggests that the mobility and bioavailability of the five metals probably decline in the following order: Cd = Pb > Ni > Cu > Zn.     

Geochemistry characterization of groundwater in an agricultural area of Razan,Hamadan, Iran

This study was conducted to evaluate factors regulating groundwater quality in an area with agriculture as main use. Thirty groundwater samples have been collected from Razan area (Hamadan, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. The chemical compositions of the groundwater are dominated by Na⁺, Ca²⁺, HCO₃ ⁻, Cl⁻ and SO₄ ²⁻, which have been derived largely from natural chemical weathering of carbonate, gypsum and anthropogenic activities of fertilizer’s source. The production of SO₄ ²⁻ has multiple origins, mainly from dissolution of sulphate minerals, oxidation of sulphide minerals and anthropogenic sources. The major anthropogenic components in the groundwater include Na⁺, Cl⁻, SO₄ ²⁻ and NO₃ ⁻, with Cl⁻ and NO₃ ⁻ being the main contributors to groundwater pollution in Razan area.     

Unstable modes of non-axisymmetric gaseous discs

We present a perturbation theory for studying the instabilities of non-axisymmetric gaseous discs. We perturb the dynamical equations of self-gravitating fluids in the vicinity of a non-axisymmetric equilibrium, and expand the perturbed physical quantities in terms of a complete basis set and a small non-axisymmetry parameter ε. We then derive a linear eigenvalue problem in matrix form, and determine the pattern speed, growth rate and mode shapes of the first three unstable modes. In non-axisymmetric discs, the amplitude and the phase angle of travelling waves are functions of both the radius R and the azimuthal angle φ. This is due to the interaction of different wave components in the response spectrum. We demonstrate that wave interaction in unstable discs, with small initial asymmetries, can develop dense clumps during the phase of exponential growth. Local clumps, which occur on the major spiral arms, can constitute seeds of gas giant planets in accretion discs.     

Effect of addition of organic residues on phosphorus release kinetics in some calcareous soils of western Iran

We investigated the effects on phosphorus (P) release of the addition of potato, wheat, and sunflower residues and fruit compost to five calcareous soils. Residue was added at the rate of 20 g kg⁻¹. After 2 months of incubation, P values in control and amended soils were used for kinetic studies and fractionated by a sequential extraction procedure. The relative contribution of available P fraction (KCl-P) increased from 1.4% in control soils to 1.8%, 1.9%, 2.2%, and 2.3% in soils amended by fruit, wheat, potato, and sunflower residue addition, respectively, indicating that organic residues increased P in this fraction. In soils amended with different residues, the percentage of Olsen-P released over 86-h successive extractions with 0.01 M CaCl₂ ranged from 57.6% for fruit residue addition (average of five soils) to 60.5% for potato residue addition. The ability of residues to release P depended on the soil properties, with 21.9 mg kg⁻¹ (average of all residues) released to soil 2 and 77.4 mg kg⁻¹ released to soil 4. Also residues behaved differently, with 31.5 mg kg⁻¹ (average of five soils) released by fruit residues and 40.0 mg kg⁻¹ released by sunflower residues. Release of P was best described by a parabolic diffusion model. The corresponding rate constant (mg kg⁻¹ h^−1/2) for P release for amended soils, defined as the release rate averaged for five soils, was found to decrease in the order: potato (2.73) > sunflower (2.61) > wheat (2.56) > fruit (2.50). The present study demonstrates that addition of residues improves P availability of these calcareous soils by increasing extractable P and the release rate and could be an alternative, indigenous source of P. However, the increase in P availability and the release rate following organic residue application suggests high potential mobility to water sources.