Sources Of Ionic Species Research Articles

Nature and sources of ionic species in rainwater during monsoon periods in and around sixteenth-seventeenth century CE monuments in Yamuna River basin, India.

The nature and sources of ionic species were studied in the monsoon rainwater collected from two monuments of the sixteenth-seventeenth century CE in the Yamuna River basin from 2016 to 2018. The results showed the acidic pH of the rainwater with high dissolved SO4-2 and NO3-, and soil-derived components (Ca+2, Mg+2, and K+). The anionic (SO4-2, NO3-, Cl-, F-, and HCO3-) and cationic (Ca+2, Mg+2, K+, NH4+, and Na+) concentrations showed regional differences in yearly contribution mainly from the fossil fuel combustion, soil dust, and farm residue burning. The rainwater analysis showed low dissolved ions at SCTK (Sheikh Chilli's Tomb, Kurukshetra) compared to KBMP (Kabuli Bagh Mosque, Panipat). The mean concentration of SO4-2 was 1.5 times higher than the NO3- apportioning the sulfate as a dominant acidifying constituent in rainwater. Pearson's correlation and principal component analysis (PCA) showed terrestrial and marine origins of dissolved ions in the rainwater. The Na-normalized molar ratios and the analysis of sea salt and non-sea salt fractions indicate the dominance of non-marine contributions in the precipitation. Based on neutralization factors, cations showed neutralization of rainwater acidity as follows: NFCa+2 > NFMg+2 > NFNH4+ > NFK+. The potential index showed the dominance of the neutralization potential (NP) on acidic potential (AP) at both locations.

Nature and Sources of Ionic Species in Precipitation across the Indo-Gangetic Plains, India

ABSTRACTThe spatial distribution of rainwater chemistry over the densely-populated and highly polluted Indo-Gangetic Plains (IGP) was investigated using samples (total = 687) collected during three consecutive summer monsoon seasons from 2009 to 2011. The concentrations of secondary ionic species (SO42– and NO3–) were measured along with the other major ions (F–, Cl–, Na+, K+, Ca2+, Mg2+ and NH4+) and pH and specific conductivity. The weighted mean pH (± std) and conductivity of rainwater were 5.73 (± 0.17) and 31.6 (± 31.0) µS cm–1, respectively. Approximately 16% of rainwater samples were acidic (pH 5.61) (mean pH = 6.34 for the more basic samples). Specific conductivity was ~39% lower (20.6 µS cm–1) for the acidic rain compared to the more basic (33.6 µS cm–1) samples. The mean sum of all of the measured ions is 351.6 ± 130.1 µeq L–1 with the highest contributions being Ca2+ (30%) and SO42– (15%). Mean [SO42–] (52 µeq L–1) and [NO3–] (29 µeq L–1) were approximately five and ten times higher, respectively, compared to background hemispheric values. Secondary ions had the highest deposition fluxes (SO42–, 25.2 kg ha–1 y–1 and NO3–: 18.3 kg ha–1 y–1). The mean ratio of H+/(NO3– + SO42–) was 0.02 indicating ~98% of the acidity was neutralized. Ca2+, (57%), Mg2 (25%), NH4+ (15%) and K+ (4%) were important neutralizing species. Positive Matrix Factorization (PMF) was applied to the deposition fluxes. Five factors were identified and identified as ammonia neutralized, sea salt, soil, biomass burning, and calcium neutralized.

Hydrochemistry of Wet Atmospheric Precipitation Over an Urban Area in Northern Indo-Gangetic Plains

Rain water samples were collected to study the chemical composition of wet atmospheric precipitation (first event) over the Lucknow city in the northern Indo-gangetic alluvial plains. The samples were collected in the month of July, 2005 from different sites. The wet precipitation samples were analyzed for pH, EC, major ions (HCO(-3), Cl(-), SO4(2-), NO(-3), PO4(-3), F(-), Na(+), K(+), Ca(2+), Mg(2+), NH4+) and heavy metals (As, Cd, Al, Co, Cr, Cu, Fe, Mn, Mo, Ni, Hg, Pb, Se, Sn, Ti, V, Zn). The pH values of wet precipitation samples ranged between 6.5 and 8.7. The analysis of linear regression applied to the set of studied variables and computation of neutralization factors showed that neutralization occurred in precipitation samples and Ca(2+) had the maximum neutralization capacity. It was found that Cl(-), [Formula: see text], Ca(2+), Mg(2+), Na(+) and K(+) in the precipitation samples originated mainly from crustal/anthropogenic sources in the region. On an average Fe, and Al accounted for >72% of the total concentration of trace metals in the wet precipitation samples followed by Zn (>10%). Enrichment factors calculated for heavy metals over reference background level in seawater and Earth's crust showed relatively higher enrichment of Zn. The principal component analysis (PCA) identified the possible sources of ionic species and heavy metals in the wet precipitation samples.