In this paper, we studied the regional aerosol and air quality over an urban location, Pune, India during the period from 8 to 18 November 2012, encompassing a major Indian celebration, namely, Diwali Festival (12–14 November 2012) and also a clean (control) day (9 November 2012). A suit of ground–based measurements, employing solar radiometers (Microtops II and Cimel Sun–sky radiometer), Nephelometer, and satellite observations carried out over the study region have been applied for these investigations. The study revealed many interesting results which include (i) almost four–fold enhancement in AOD and fine mode dominated aerosol size distribution (ASD) during Diwali compared to clean day conditions; (ii) higher columnar water vapor (H2O), nitrogen dioxide (NO2), and lower ozone (O3) during Diwali period; (iii) higher cooling at bottom (–117W m−2) and top of the atmosphere (–33W m−2) and warming (+82W m−2) in the atmosphere during the festival period, (iv) abundance of fine mode anthropogenic scattering particles associated with greater real part and smaller imaginary part of refractive index, and higher single scattering albedo, (v) higher backscattering coefficient revealing intrusion of more aerosol particles, higher depolarization ratio indicating particles of non–spherical nature, presence of water–phase particles, more polluted smoke and dust particles, (vi) greater attenuation and poor horizontal/vertical visibility, and (vii) dominance of urban industrial/biomass burning aerosols among other aerosol types. These results have been compared with concurrent satellite products and found to be consistent. The results have been further explained with local meteorology, back–trajectory analysis and satellite rapid response images.

Increased frequency and enhanced damage to the marine environment and to human society caused by green macroalgae blooms demand improved high-resolution early detection methods. Conventional satellite remote sensing methods via spectra radiometers do not work in cloud-covered areas, and therefore cannot meet these demands for operational applications. We present a methodology for green macroalgae bloom detection based on RADARSAT-2 synthetic aperture radar (SAR) images. Green macroalgae patches exhibit different polarimetric characteristics compared to the open ocean surface, in both the amplitude and phase domains of SAR-measured complex radar backscatter returns. In this study, new index factors are defined which have opposite signs in green macroalgae-covered areas, compared to the open water surface. These index factors enable unsupervised detection from SAR images, providing a high-resolution new tool for detection of green macroalgae blooms, which can potentially contribute to a better understanding of the mechanisms related to outbreaks of green macroalgae blooms in coastal areas throughout the world ocean.

The photochemical degradation of two widely used organophosphorothioate insecticides, fenitrothion and diazinon, was investigated in aqueous solutions containing three separate dissolved constituents commonly found in natural waters (NO 3 − , CO 3 2− and dissolved organic matter (DOC)). The effect of these constituents on pesticide photodegradation was compared to degradation in “constituent-free” pure water. Solutions were irradiated in an Atlas solar simulator fitted with a UV-filtered Xenon arc lamp with light irradiances (500 W m−2) measured using a spectral radiometer to allow derivation of quantum yields of degradation. Fenitrothion absorbs light within the solar UV range (λ, 295–400 nm) and underwent direct photolysis in pure water whereas diazinon (λ max ∼250 nm) showed no observable loss over the experimental period. However, photodegradation conforming to pseudo-first-order kinetics was observed for both chemicals in the presence of the dissolved constituents (at concentrations typically observed in natural waters), with the rates of photodecay observed in the order of NO 3 − > CO 3 2− ≅ DOC, with the highest rates observed in the 3 mM NO 3 − solutions (k Fen = 0.155 ± 0.041 h−1; k Dia = 0.084 ± 0.0007 h−1). For diazinon this rate was comparable to fenitrothion photolysis in pure water (k fen 0.072 ± 0.0078 h−1), highlighting the importance of NO 3 − on a non-photolabile pesticide, with indirect photodegradation probably attributable to the light-induced release of aqueous hydroxyl radicals (·OH) from NO 3 − . Suwannee river fulvic acid (serving as DOC) did not statistically affect the rate of photodecay for fenitrothion relative to its photolysis in MilliQ water, although measured rates in DOC solutions were slightly lower. However, measurable rates of photodecay were apparent for diazinon in the DOC solutions, indicating that fulvic acid, possibly in the form of “excited” triplet-state-DOC plays a role in diazinon transformation. Hydrolysis was not apparent for fenitrothion (in buffered solutions of pH 5–9) but was notable for diazinon at the lower pHs of 5 and 3 (k Dia-hyd 0.3414 h−1 at pH 3 and 0.228 h−1 at pH 5), resulting in the formation of the degradate, 2-isopropyl–6-methyl–4-pyrimidinol. This work highlights the importance of dissolved constituents on abiotic photodegradation of pesticides and it is recommended that these constituents be incorporated into laboratory-based fate-testing regimes.