Vinod Tare
Indian Institute of Technology Kanpur
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Publication
Featured researches published by Vinod Tare.
Geophysical Research Letters | 2005
S. N. Tripathi; Sagnik Dey; Vinod Tare; S. K. Satheesh
During a comprehensive aerosol field campaign as part of ISRO-GBP,extensive measurements of aerosol black carbon were made during December 2004, for the first time, at Kanpur, an urban continent allocation in northern India. BC diurnal variation is associated with changes in boundary layer mixing and anthropogenic activities. BC concentration in Kanpur is comparable to those measured in other megacities of India but much higher than in similar locations of Europe,USA and Asia. High BC concentration is found both in absolute terms
Environmental Science & Technology | 2011
Daya S. Kaul; Tarun Gupta; S. N. Tripathi; Vinod Tare; J. L. Collett
(6-20 \mu g m^{-3} )
Bioresource Technology | 2011
Subrata Hait; Vinod Tare
and mass fraction (similar to 10%) yielding very low single scattering albedo (0.76). The estimated surface forcing is as high as
Waste Management | 2010
Kunwar D. Yadav; Vinod Tare; M. Mansoor Ahammed
-62 +/- 23 W m^{-2}
Ecotoxicology and Environmental Safety | 2012
Subrata Hait; Vinod Tare
and top of the atmosphere (TOA) forcing is
Journal of The Air & Waste Management Association | 2003
Vinod Tare; Sandeep Gupta; Purnendu Bose
+9 +/- 3 W m^{-2}
Waste Management | 2011
Subrata Hait; Vinod Tare
, which means the atmospheric absorption is
Journal of remote sensing | 2007
Anup K. Prasad; Ramesh P. Singh; Vinod Tare; Menas Kafatos
+71 Wm^{-2}
Bioresource Technology | 2000
Mohammad Jawed; Vinod Tare
. The short wave atmospheric absorption translates to a lower atmospheric heating of similar to 1.8 degrees K/day. Large surface cooling and lower atmospheric heating may have impacts to regional climate.
Journal of Applied Polymer Science | 1999
Sanjeev Chaudhari; Vinod Tare
Carbonaceous species, meteorological parameters, trace gases, and fogwater chemistry were measured during winter in the Indian city of Kanpur to study secondary organic aerosol (SOA) during foggy and clear (nonfoggy) days. Enhanced SOA production was observed during fog episodes. It is hypothesized that aqueous phase chemistry in fog drops is responsible for increasing SOA production. SOA concentrations on foggy days exceeded those on clear days at all times of day; peak foggy day SOA concentrations were observed in the evening vs peak clear day SOA concentrations which occurred in the afternoon. Changes in biomass burning emissions on foggy days were examined because of their potential to confound estimates of SOA production based on analysis of organic to elemental carbon (OC/EC) ratios. No evidence of biomass burning influence on SOA during foggy days was found. Enhanced oxidation of SO(2) to sulfate during foggy days was observed, possibly causing the regional aerosol to become more acidic. No evidence was found in this study, either, for effects of temperature or relative humidity on SOA production. In addition to SOA production, fogs can also play an important role in cleaning the atmosphere of carbonaceous aerosols. Preferential scavenging of water-soluble organic carbon (WSOC) by fog droplets was observed. OC was found to be enriched in smaller droplets, limiting the rate of OC deposition by droplet sedimentation. Lower EC concentrations were observed on foggy days, despite greater stagnation and lower mixing heights, suggesting fog scavenging and removal of EC was active as well.