Environmental study of two significant solid samples: gravitation dust sediment and soil

In this work are presented results of the complex study of two significant solid environmental samples: gravitation dust sediments (industrial pollutants, potential source of risk elements input to soils) and soils (component of the environment, potential source of risk elements input to food web). The first phase of this study was focused on the study of the significant chemical properties (phase composition, content of organic and inorganic carbon) of the dust and soil samples. In the second phase, the fractionation analysis was used on the evaluation of the mobility of chosen risk elements (Cu, Ni, Pb, Zn) in the studied samples. The single-step extractions were applied in the order of the isolation of the element forms (fractions), with different mobilities during defined ecological conditions by utilization of the following reagents: 1 mol dm^− 3 NH₄NO₃ for isolation of the “mobile” fraction, 0.05 mol dm^− 3 ethylenediaminetetraacetic acid and 0.43 mol dm^− 3 CH₃COOH for isolation of the “mobilizable” fraction, and 2 mol dm^− 3 HNO₃ for isolation of all releasable forms. On the basis of the results obtained in this study, it is possible to state that different origins and positions of solid environmental samples in the environment reflect in different chemical properties of their matrix. The different properties of the sample matrix result in different mobilities of risk elements in these kinds of samples. The fractionation analysis with single-step extraction for isolation element fractions is the method most suitable for easy checking of environmental pollution and for evaluation of risk elements cycle in the environment.     

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.     

Assessment of the sources of suspended particulate matter aerosol using US EPA PMF 3.0

The main purpose of this paper was to carry out a source apportionment of suspended particulate matter (SPM) samples using positive matrix factorization procedure. The central and local Government of Japan introduced strict emission regulations in 2002/10 and 2003/10, respectively, in curbing SPM pollution from major metropolitans. This paper also highlighted the impact of the measures taken by the central and local Government of Japan on the reduction of SPM and the contributions of sources. SPM samples were collected for 6 years starting from 1999 to 2005 at two sites, i.e., site A (urban) and site B (suburban) of Yokohama, Japan. Microwave digestion and inductively coupled plasma-mass spectroscopy (ICP-MS) were employed to measure Mg, Al, Ca, V, Cr, Mn, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Pb and Bi, while water soluble ions (Na⁺, NH₄  ⁺_{4}^{\ \,+}, K⁺, Ca^2 +, Mg^2 +, Cl⁻, NO₃  ^-_{3}^{\ \,-} and SO₄  ^2-)_{4}^{\ \,2-}) as well as carbonaceous mass (EC and OC) were analyzed using ion chromatograph and CHN analyzer, respectively. The sources identified at two sites were automobile, soil dust, marine aerosol, mixed sources, and secondarily formed aerosol. Also, source quantification was performed. Automobile and soil dust were striking contributors at site A. Automobile and soil dust of SPM aerosol might be produced from local origin at current study areas. Besides, Asian dust had an impact on high concentrations of SPM aerosol in some certain period of the year due to the outflows of East Asian emission. In contrast, secondary aerosol in the form of sulfate and ammonium as well as mixed sources (coal, long-transported Cs, and other unknown sources) were remarkable at site B. Stationary/industrial combustion has apparently more impact on the release of SPM components at site B than A. Automobile regulations in 2002 and 2003, respectively, resulted in reduction of SPM by 28% for site A and 16% for site B. There was also net reduction of automobile contribution at both sites due to the above measures being implemented.     

Geochemical position of Pb,Zn and Cd in soils near the Olkusz mine/smelter,South Poland: effects of land use,type of contamination and distance from pollution source

The soils adjacent to an area of historical mining, ore processing and smelting activities reflects the historical background and a mixing of recent contamination sources. The main anthropogenic sources of metals can be connected with historical and recent mine wastes, direct atmospheric deposition from mining and smelting processes and dust particles originating from open tailings ponds. Contaminated agriculture and forest soil samples with mining and smelting related pollutants were collected at different distances from the source of emission in the Pb–Zn–Ag mining area near Olkusz, Upper Silesia to (a) compare the chemical speciation of metals in agriculture and forest soils situated at the same distance from the point source of pollution (paired sampling design), (b) to evaluate the relationship between the distance from the polluter and the retention of the metals in the soil, (c) to describe mineralogy transformation of anthropogenic soil particles in the soils, and (d) to assess the effect of deposited fly ash vs. dumped mining/smelting waste on the mobility and bioavailability of metals in the soil. Forest soils are much more affected with smelting processes than agriculture soils. However, agriculture soils suffer from the downward metal migration more than the forest soils. The maximum concentrations of Pb, Zn, and Cd were detected in a forest soil profile near the smelter and reached about 25 g kg^− 1, 20 g kg^− 1 and 200 mg kg^− 1 for Pb, Zn and Cd, respectively. The metal pollutants from smelting processes are less stable under slightly alkaline soil pH then acidic due to the metal carbonates precipitation. Metal mobility ranges in the studied forest soils are as follows: Pb > Zn ≈ Cd for relatively circum-neutral soil pH (near the smelter), Cd > Zn > Pb for acidic soils (further from the smelter). Under relatively comparable pH conditions, the main soil properties influencing metal migration are total organic carbon and cation exchange capacity. The mobilization of Pb, Zn and Cd in soils depends on the persistence of the metal-containing particles in the atmosphere; the longer the time, the more abundant the stable forms. The dumped mining/smelting waste is less risk of easily mobilizable metal forms, however, downward metal migration especially due to the periodical leaching of the waste was observed.     

Heavy metal contamination from mining sites in South Morocco: Monitoring metal content and toxicity of soil runoff and groundwater

The aim of the present work is the assessment of metal toxicity in runoff, in their contaminated soils and in the groundwater sampled from two mining areas in the region of Marrakech using a microbial bioassay MetPLATE™. This bioassay is based on the specific inhibition of the β-galactosidase enzyme of a mutant strain of Escherichia coli, by the metallic pollutants. The stream waters from all sampling stations in the two mines were all very toxic and displayed percent enzyme inhibition exceeding 87% except SWA₄ and SWB₁ stations in mine C. Their high concentrations of copper (Cu) and zinc (Zn) confirm the acute toxicity shown by MetPLATE. The pH of stream waters from mine B and C varied between 2.1 and 6.2 and was probably responsible for metal mobilization, suggesting a problem of acid mine drainage in these mining areas. The bioassay MetPLATE™ was also applied to mine tailings and to soils contaminated by the acidic waters. The results show that the high toxicity of these soils and tailings was mainly due to the relatively concentration of soluble Zn and Cu. The use of MetPLATE™ in groundwater toxicity testing shows that, most of the samples exhibited low metal toxicity (2.7–45.5% inhibition) except GW3 of the mine B (95.3% inhibition during the wet season and 82.9% inhibition during the dry season). This high toxicity is attributed to the higher than usual concentrations of Cu (189 μg Cu l⁻¹) and Zn (1505 μg Zn l⁻¹). These results show the potential risk of the contamination of different ecosystems situated to the vicinity of these two metalliferous sites. The general trend observed was an increase in metal toxicity measured by the MetPLATE with increasing total and mobile metal concentrations in the studied matrices. Therefore, the MetPLATE bioassay is a reliable and fast bioassay to estimate the metals toxicity in the aquatic and solids samples.     

Major ion chemistry of shallow groundwater of a fast growing city of Central India

Nagpur City located in semiarid area of central India is a fast-growing industrial centre. In recent years, rapid development has created an increased demand for drinking water, which is increasingly being fulfilled by groundwater abstraction. The present study was undertaken to assess major ion chemistry of shallow groundwater to understand geochemical evolution of groundwater and water quality for promoting sustainable development and effective management of groundwater resources. A total of 47 water samples were collected from shallow aquifer of selected parts of the city and the water chemistry of various ions viz. Ca^2 +, Mg^2 +, Na⁺, K⁺, CO₃  ^2-_{3}^{\ \, 2-}, HCO₃  ^-_{3}^{\ \, -}, Cl⁻, SO₄  ^2-_{4}^{\ \,2-} and NO₃  ^-_{3}^{\ \,-} are carried out. The chemical relationships in Piper diagram identify Ca–HCO₃–Cl and mixed Ca–Na–HCO₃–Cl as most prevalent water types. Alkaline earth exceeds alkalis and weak acids exceed strong acids. Ionic ratios and Gibb’s diagram suggest that silicate rock weathering and anthropogenic activities are the main processes that determine the ionic composition in the study area. The nitrate appeared as a major problem of safe drinking water in this region. We recorded highest nitrate concentration, i.e., 411 mg/l in one of the dug well. A comparison of groundwater quality in relation to drinking water quality standards revealed that about half of the shallow aquifer samples are not suitable for drinking.     

Determination of road dust loadings and chemical characteristics using resuspension

The contribution of fugitive dust from traffic to air pollution can no longer be ignored in China. In order to obtain the road dust loadings and to understand the chemical characteristics of PM₁₀ and PM_2.5 from typical road dust, different paved roads in eight districts of Beijing were selected for dust collection during the four seasons of 2005. Ninety-eight samples from 28 roads were obtained. The samples were resuspended using equipment assembled to simulate the rising process of road dust caused by the wind or wheels in order to obtain the PM₁₀ and PM_2.5 filter samples. The average road dust loading was 3.82 g m^− 2, with the highest of 24.22 g m^− 2 being in Hutongs in the rural–urban continuum during winter. The road dust loadings on higher-grade roads were lower than those on lower-grade roads. Attention should be paid to the pollution in the rural–urban continuum areas. The sums of element abundances measured were 16.17% and 18.50% for PM₁₀ and PM_2.5 in road dust. The average abundances of OC and EC in PM₁₀ and PM_2.5 in road dust were 11.52%, 2.01% and 12.50%, 2.06%, respectively. The abundance of elements, water-soluble ions, and OC, EC in PM₁₀ and PM_2.5 resuspended from road dust did not change greatly with seasons and road types. The soil dust, construction dust, dust emitted from burning coal, vehicle exhaust, and deposition of particles in the air were the main sources of road dust in Beijing. Affected by the application of snow-melting agents in Beijing during winter, the amount of Cl⁻ and Na⁺ was much higher during that time than in the other seasons. This will have a certain influence on roads, bridges, vegetations, and groundwater.     

Pasture composition in a trace element-contaminated area: the particular case of Fe and Cd for grazing horses

Pasture selection by livestock is an essential topic for rangeland management, especially in trace element-contaminated soils. We have studied the composition (nutrients and trace elements) of a grass-based diet from soils affected by a mine spill at different growth stages (October 2008 to May 2009). A diet based on other plants (mainly Compositae species) was also studied (May 2009) for comparison. Faeces and mane hair of horses feeding on these pastures were also analysed. Micronutrient (Cu, Fe, Mn and Zn) and potentially toxic trace element (As, Cd, Pb, Tl) concentrations were below the maximum tolerable levels (MTL) for horses, except for Fe (at early growth of pastures) and Cd (in the diet based on ‘other’ plants). Values of potential ingestion of Fe by horses were higher than 10 mg kg body weight^− 1 day^− 1. Cadmium concentrations in some pasture samples (those composed of Compositae species) were higher than 3 mg kg^− 1. Potential toxicity of such Cd levels in pastures is uncertain, since a high disparity of criteria about MTL by cattle exists (between 0.5 and 10 mg kg^− 1 diet). Nutrient concentrations were adequate for horses, which could counteract possible harmful effects derived from trace element ingestion. The analyses of excreta and mane hair point to the low risk of toxicity derived from the consumption of these contaminated pastures. However, the ingestion of regenerating pastures (autumnal samples) should be avoided due to the greater risk of ingestion of contaminated soil attached to the plant material. Management of these pastures by grazing requires periodic monitoring. Special attention should be given to Fe and particularly Cd (non-essential element) which accumulates in animal organs, where it could provoke uncertain long-term effects.     

Rinodina sophodes (Ach.) Massal.: a bioaccumulator of polycyclic aromatic hydrocarbons (PAHs) in Kanpur City, India

The aim of this study is to determine the possibility of using Rinodina sophodes (Ach.) Massal., a crustose lichen as polycyclic aromatic hydrocarbons (PAHs) bioaccumulator for evaluation of atmospheric pollution in tropical areas of India, where few species of lichens are able to grow. PAHs were identified, quantified and compared to evaluate the potential utility of R. sophodes. The limit of detection for different PAHs was found to be 0.008–0.050 μg g^− 1. The total PAHs in different sites were ranged between 0.189 ± 0.029 and 0.494 ± 0.105 μg g^− 1. The major sources of PAHs were combustion of organic materials, traffic and vehicular exhaust (diesel and gasoline engine). Significantly higher concentration of acenaphthylene and phenanthrene indicates road traffic as major source of PAH pollution in the city. Two-way ANOVA also confirms that all PAHs content showed significant differences between all sampling sites (P 1%). This study establishes the utility of R. sophodes in monitoring the PAHs accumulation potentiality for development of effective tool and explores the most potential traits resistant to the hazardous environmental conditions in the tropical regions of north India, where no such other effective way of biomonitoring is known so far.     

Spatial and seasonal variability of pore water phosphorus concentration in shallow Lake Swarzędzkie,Poland

Pore waters play an important role in phosphorus dynamics in aquatic ecosystems. Phosphorus concentrations in pore waters are much higher than above the bottom. This is confirmed by the results of this study concerning the hypereutrophic lake. Pore water was analyzed at 11 sampling stations in the upper layer of bottom sediments. This water was separated by centrifugation and phosphorus level was measured spectrophotometrically with ascorbic acid as a reducer. Total phosphorus concentration in pore waters ranged from 0.5 to 8.1 mgP l^− 1 (mean 3.2 mgP l^− 1). Mean phosphorus concentration in pore water samples of this lake was the highest in summer and the lowest in winter. High concentrations were observed in samples from the pelagial and low from the macrophyte zone.     

Water quality and dissolved inorganic fluxes of N,P, SO<Subscript>4</Subscript>, and K of a small catchment river in the Southwestern Coast of India

The southwestern coast of India is drained by many small rivers with lengths less than 250 km and catchment areas less than 6,500 km². These rivers are perennial and are also the major drinking water sources in the region. But, the fast pace of urbanization, industrialization, fertilizer intensive agricultural activities and rise in pilgrim tourism in the past four to five decades have imposed marked changes in water quality and solute fluxes of many of these rivers. The problems have aggravated further due to leaching of ionic constituents from the organic-rich (peaty) impervious sub-surface layers that are exposed due to channel incision resulting from indiscriminate instream mining for construction-grade sand and gravel. In this context, an attempt has been made here to evaluate the water quality and the net nutrient flux of one of the important rivers in the southwestern coast of India, the Manimala river which has a length of about 90 km and catchment area of 847 km². The river exhibits seasonal variation in most of the water quality parameters (pH, electrical conductivity, dissolved oxygen, total dissolved solids, Ca, Mg, Na, K, Fe, HCO₃, NO₂-N, NO₃-N, P _\text-inorg_{\rm \text{-}inorg}, P _\text-tot_{\rm \text{-}tot}, chloride, SO₄, and SiO₂). Except for NO₃-N and SiO₂, all the other parameters are generally enriched in non-monsoon (December–May) samples than that of monsoon (June–November). The flux estimation reveals that the Manimala river transports an amount of 2,308 t y^− 1 of dissolved inorganic nitrogen, 87 t y^− 1 dissolved inorganic phosphorus, and 9246 t y^− 1 of SO₄, and 1984 t y^− 1 K into the receiving coastal waters. These together constitute about 23% of the total dissolved fluxes transported by the Manimala river. Based on the study, a set of mitigation measures are also suggested to improve the overall water quality of small catchment rivers of the densely populated tropics in general and the south western coast in particular.     

Determination of ametryn in sugarcane and ametryn–atrazine herbicide formulations using spectrophotometric method

A sensitive spectrophotometric method has been developed for determination of ametryn in agricultural samples. The proposed method was based on reaction with pyridine and further coupling with sulfanilic acid to form a colored product. The absorbance was measured at 400 nm with a molar absorptivity of 2.1 × 10⁵ L mol⁻¹ cm⁻¹. The method shows a linear range from 0.2–20 μg mL⁻¹ with limit of detection and limit of quantification 0.16 and 0.54 μg mL⁻¹, respectively. The method has been successfully applied to the determination of ametryn in sugarcane juice and commercial formulations after separation of ametryn from triazine herbicides based on solvent extraction. Recovery values were found to be in the range of 96.0 ± 0.2% to 98.4 ± 0.1%.     

Organochlorine pesticides and polychlorinated biphenyls in common buzzard (<Emphasis Type="Italic">Buteo buteo</Emphasis>) from Sicily (Italy)

In the present study, we investigated the concentrations and distribution of organochlorine pesticides (OCs) and polychlorinated biphenyls (PCBs) in intestine, liver, and muscle samples of 11 common buzzards (Buteo buteo) from Sicily used as bioindicator for monitoring pollution in environment. All samples of common buzzards were collected at the “Recovery Center of Wild Fauna” of Palermo, through the Zooprophilactic Institute. Quantitative determination of OCs and PCBs in the samples examined has been carried out using HRGC-ECD and GC-MS. The results obtained show the presence of concentrations of ∑DDT and ∑PCB in almost all samples. Regarding ∑DDT (4,4^′-DDE, 2,4^′-DDD, 4,4^′-DDD, 2,4^′-DDT, and 4,4^′-DDT), the highest concentrations were found in intestine (0.411 ± 0.050 μg/g) followed by muscle (0.130 ± 0.017 μg/g) and liver samples (0.109 ± 0.014 μg/g). As regards the ∑PCB congeners (PCB-28, PCB-52, PCB-95, PCB-99, PCB-101, PCB-110, PCB-138, PCB-146, PCB-149, PCB-151, PCB-153, PCB-170, PCB-177, PCB-180, PCB-183, and PCB-187), the highest concentrations were found in intestine (1.686 ± 0.144 μg/g) followed by liver (1.064 ± 0.162 μg/g) and muscle samples (0.797 ± 0.078 μg/g). Our data deserve particular attention not only for their significance but especially because they were recorded in Sicily, a region with a very low risk of environmental pollution due to the shortage of industries.     

Variations in sensitivity of two populations of Corophium Orientale (Crustacea: Amphipoda) towards cadmium and sodium laurylsulphate

The aim of this work was to monitor the sensitivity of two populations of Corophium orientale (Crustacea: Amphipoda) living at the outfall of two rivers (Magra and Serchio), comparing their responses towards two different toxicant solutions. Sensitivity was monthly checked performing the 96h-LC₅₀ static water only test with Cd(NO₃)₂ and SDS. If no significant differences were found between the two populations, they could have been employed without distinction to perform sediment toxicity bioassays. As regard to Cd, an increasing in LC₅₀ values from summer to winter was evident in each population (Serchio River: August 2003  =  1,36 mg/l, February 2004  =  7,23 mg/l; Magra River: August  =  1,21 mg/l, April  =  5,01 mg/l). This pattern was correlated to the droop of temperatures in winter period. The responses of the two populations towards the cadmium were compared using the ANOVA. The analysis showed any significant differences between the populations (p  =  0.12). The pattern of sensitivity towards SDS for the population living on Magra River was similar to the same pattern found for Cd; as regard to the population living on Serchio River, data were not enough to describe the annual pattern. Anyway, statistical analysis was performed and no significant differences were found between the two populations (p  =  0.34).     

A spectrophotometric assay method for vanadium in biological and environmental samples using 2,4-dinitrophenylhydrazine with imipramine hydrochloride

A simple, rapid, and sensitive method involving the interaction of 2,4-dinitrophenylhydrazine with imipramine hydrochloride in presence of vanadium (V) in sulfuric acid medium has been proposed for the determination of vanadium. The purple-colored product developed showed an absorption maximum at 560 nm and was stable for 24 h. The working curve was linear over the concentration range of 0.1–2.8 μg ml^− 1, with sensitivity of detection of 0.0124 μg ml^− 1. Molar absorptivity and Sandell’s sensitivity were found to be 2.6 × 10⁴ l/mol cm and 0.0039 μg cm^− 1, respectively. The accuracy of the proposed method was assessed by Student’s t test and variance ratio F test, and the results were on par with the reported method. The method was successfully used in the determination of V in water, human urine, soil, and plant samples, and it was free from interference by various concomitant ions.     

Risk assessment due to intake of heavy metals through the ingestion of groundwater around two proposed uranium mining areas in Jharkhand,India

Heavy metal pollution of water resources can be apprehended in East Singhbhum region which is a highly mineralised zone with extensive mining of copper, uranium and other minerals. Ten groundwater samples were collected from each site and the heavy metal analysis was done by atomic absorption spectrophotometer. Analysis of the results of the study reveals that the concentration of iron, manganese, zinc, lead, copper and nickel in groundwater of Bagjata mining area ranged 0.06–5.3 mg l^− 1, 0.01–1.3 mg l^− 1, 0.02–8.2 mg l^− 1, 1.4–28.4 μg l^− 1, 0.78–20.0 μg l^− 1 and 1.05–20.1 μg l^− 1, respectively. In case of Banduhurang mining area, the range was 0.04–2.93 mg l^− 1, 0.02–1.1 mg l^− 1, 0.01–4.68 mg l^− 1, 1.04–33.21 μg l^− 1, 1.24–18.7 μg l^− 1 and 1.06–14.58 μg l^− 1, respectively. The heavy metals were found to be below the drinking water standards (IS:10500 1993) except iron (0.3 mg l^− 1) and manganese (0.1 mg l^− 1). The hazard quotients of the heavy metals for drinking water were below 1 posing no threat due to intake of water to the people for both the areas.     

Bio-concentration of chromium—an <Emphasis Type="Italic">in situ</Emphasis> phytoremediation study at South Kaliapani chromite mining area of Orissa,India

Mine waste water at South Kaliapani usually contains toxic levels of hexavalent Cr(VI). The present in situ study was conducted at South Kaliapani chromite mine area in Orissa state, India, to assess the phytoremediation ability of three plants, namely, rice (Oryza sativa L.), paragrass (Brachiaria mutica), and an aquatic weed (Eichhornia crassipes), in attenuating Cr(VI) from mine waste water and to correlate the bio-concentration factors (BCF) of Cr. Water hyacinth (E. crassipes) showed 24% to 54% reduction whereas paragrass (B. mutica) was able to reduce 18% to 33% of Cr(VI) from mine water. This reduction was studied over a period of 100 days of plant growth. The reduction was observed through a passage of a sum total of 2,000 sq. ft. cultivated plots and ponds separately. Reduction in Cr(VI) content in mine water varies with plant age as well as with the distance of passage. Cr accumulation and BCF values increased with high soil Cr levels as well as the age of plants. High BCF and transportation index (Ti) values, i.e., 10,924 and 32.09, respectively, were noted for water hyacinth. The Ti values indicated that the root-to-shoot translocation of Cr was very high after 100 days of growth. The total accumulation rate was maximum (8.29 mg Cr kg dry biomass^− 1 day ^− 1) in paragrass. The BCF values for roots were noted to be higher than those of leaves, stems, and grains of the 125-day-old plants. Hence, paragrass and water hyacinth may be used as tools of phytoremediation to combat the problem of in situ Cr contamination.     

Greenhouse gas mitigation in rice–wheat system with leaf color chart-based urea application

Conventional blanket application of nitrogen (N) fertilizer results in more loss of N from soil system and emission of nitrous oxide, a greenhouse gas (GHG). The leaf color chart (LCC) can be used for real-time N management and synchronizing N application with crop demand to reduce GHG emission. A 1-year study was carried out to evaluate the impact of conventional and LCC-based urea application on emission of nitrous oxide, methane, and carbon dioxide in a rice–wheat system of the Indo-Gangetic Plains of India. Treatments consisted of LCC scores of ≤4 and 5 for rice and wheat and were compared with conventional fixed-time N splitting schedule. The LCC-based urea application reduced nitrous oxide emission in rice and wheat. Application of 120 kg N per hectare at LCC ≤ 4 decreased nitrous oxide emission by 16% and methane by 11% over the conventional split application of urea in rice. However, application of N at LCC ≤ 5 increased nitrous oxide emission by 11% over the LCC ≤ 4 treatment in rice. Wheat reduction of nitrous oxide at LCC ≤ 4 was 18% as compared to the conventional method. Application of LCC-based N did not affect carbon dioxide emission from soil in rice and wheat. The global warming potential (GWP) were 12,395 and 13,692 kg CO₂ ha⁻¹ in LCC ≤ 4 and conventional urea application, respectively. Total carbon fixed in conventional urea application in rice–wheat system was 4.89 Mg C ha⁻¹ and it increased to 5.54 Mg C ha⁻¹ in LCC-based urea application (LCC ≤ 4). The study showed that LCC-based urea application can reduce GWP of a rice–wheat system by 10.5%.     

Determination of cobalt,nickel and iron at trace level in natural water samples by in-column chelation-reversed phase high-performance liquid chromatography

This paper reports the utilization of 4-(2-pyridylazo) resorcinol (PAR) as a chelating reagent for in-column derivatization and the determination of trace Co, Fe, and Ni ions by reversed-phase high-performance liquid chromatography with photodiode array detector. A good separation of Co, Fe, and Ni chelates were achieved by using an Inertsil ODS-3 column and a mobile phase, consisted of methanol–THF–water mixture (50:5:45) containing ammonium acetate buffer (pH 5.0) and PAR. After full optimization, good repeatability of retention times (relative standard deviation (RSD) < 0.05%) and peak areas (RSD < 1.7%) was achieved as well as a good linearity (r ² > 0.9991). The detection limits (S/N = 3), expressed as micrograms per liter, were 0.50 (Co), 9.07 (Fe), and 2.00 (Ni). The applicability and the accuracy of the developed method were estimated by the analysis of spiked water samples and certified reference material BCR 715 wastewater-SRM.     

Evaluation of groundwater suitability for domestic,irrigational, and industrial purposes: a case study from Thirumanimuttar river basin,Tamilnadu, India

The Thirumanimuttar sub-basin forms an important groundwater province in south India, facing serious deficiency in both quality and quantity of groundwater due to increased demand associated with rapid population explosion, agricultural growth and industrial activities. A total of 194 groundwater samples were collected and 15 water quality parameters were analyzed using standard procedures. Na⁺, Cl⁻, Ca^2 +, HCO₃^-_{3}^{-}, Mg^2 + and SO₄^2-_{4}^{2-} concentration ions are more dominant in both seasons. The total dissolved solids and electrical conductivity was observed good correlation with Na⁺, Cl⁻, HCO₃^-_{3}^{-}, Ca^2 +, Mg^2 +, Cl⁻, PO₄^3-_{4}^{3-} and NO₃^- _{3}^{- } ions indicating dominance of plagioclase feldspar weathering, anthropogenic input and over drafting of groundwater irrespective of seasons. The Hill–Piper diagram indicates alkaline earths exceed the alkalis, an increase of weak acids was noted during both the seasons. For assessing the groundwater for irrigation suitability parameters like total hardness, sodium adsorption ratio, residual sodium carbonate (RSC), permeability index, and sodium percentage are also calculated. Permanent hardness was noted in higher during both the seasons due to discharge of untreated effluents and ion exchange process. The RSC indicates 56% of the samples are not suitable for irrigation purposes in both seasons, if continuously used will affect the crop yield. From the results, nearly 72% of the samples are not suitable for irrigation.