85 research outputs found
Abundance and distribution of gaseous ammonia and particulate ammonium at Delhi, India
This study reports abundance and distribution of gaseous NH<sub>3</sub> and particulate NH<sub>4</sub><sup>&plus;</sup> at Delhi. Gaseous NH<sub>3</sub> and particulate NH<sub>4</sub><sup>&plus;</sup> concentrations were measured during pre-monsoon, monsoon and post-monsoon seasons of the years 2010 and 2011. Average concentrations of gaseous NH<sub>3</sub> during pre-monsoon, monsoon and post-monsoon seasons were recorded as 26.4, 33.2 and 32.5 μg m<sup>−3</sup>, respectively. Gaseous NH<sub>3</sub> concentrations were the highest during monsoon, thought to be due to decay and decomposition of plants and other biogenic material under wet conditions, leading to increased NH<sub>3</sub> emission. The results showed that particulate NH<sub>4</sub><sup>&plus;</sup> was always lower than the gaseous NH<sub>3</sub> during all the seasons. The concentrations of particulate NH<sub>4</sub><sup>&plus;</sup> were recorded as 11.6, 22.9 and 8.5 μg m<sup>−3</sup> during pre-monsoon, monsoon and post-monsoon seasons, respectively. The percent fraction of particulate NH<sub>4</sub><sup>&plus;</sup> was noticed to be highest during the monsoon season, which is attributed to increased humidity levels favouring partitioning into the aerosol phase. On an average, 33.3% of total N-NH<sub>x</sub> was present as particulate NH<sub>4</sub><sup>&plus;</sup>. Higher concentrations of NH<sub>3</sub> noticed during night time may be due to stable atmospheric conditions. The study highlighted that, as compared with rural sites, urban sites showed higher concentrations of gaseous NH<sub>3</sub> in India, which may be due to higher population density, human activities and poor sanitation arrangements
Chemical characteristics of PM<SUB>10</SUB> aerosols and airmass trajectories over Bay of Bengal and Arabian sea during ICARB
For the first time, chemical characterization of
PM10 aerosols was attempted over the Bay of Bengal
(BoB) and Arabian Sea (AS) during the ICARB campaign.
Dominance of SO42-,
NH4+ and NO3- was
noticed over both the regions which indicated the presence of
ammonium sulphate and ammonium nitrate as major water soluble
particles playing a very important role in the radiation
budget. It was observed that all the chemical constituents
had higher concentrations over Bay of Bengal as compared to
Arabian Sea. Higher concentrations were observed near the
Indian coast showing influence of landmass indicating that
gaseous pollutants like SO2, NH3 and NO
x are transported over to the sea regions which
consequently contribute to higher
SO42-, NH4+ and
NO3- aerosols respectively. The most
polluted region over BoB was 13°-19°N and
70°-90°E while it was near 11°N and 75°E
over AS. Although the concentrations were higher over Bay of
Bengal for all the chemical constituents of PM10
aerosols, per cent non-sea salt (nss) fraction (with respect
to Na) was higher over Arabian Sea. Very low Ca2+
concentration was observed at Arabian Sea which led to higher
atmospheric acidity as compared to BoB. Nss
SO42-alone contributed 48% of total
water soluble fraction over BoB as well as AS. Ratios
SO42- /NO3- over
both the regions (7.8 and 9 over BoB and AS respectively)
were very high as compared to reported values at land sites
like Allahabad (0.63) and Kanpur (0.66) which may be due to
very low NO.3 over sea regions as compared to land sites. Air
trajectory analysis showed four classes: (i) airmass passing
through Indian land, (ii) from oceanic region, (iii) northern
Arabian Sea and Middle East and (iv) African continent. The
highest nss SO42- was observed during
airmasses coming from the Indian land side while lowest
concentrations were observed when the air was coming from
oceanic regions. Moderate concentrations of nss
SO2- 4 were observed when air was seen
moving from the Middle East and African continent. The pH of
rainwater was observed to be in the range of 5.9-6.5 which is
lower than the values reported over land sites. Similar
feature was reported over the Indian Ocean during INDOEX
indicating that marine atmosphere had more free acidity than
land atmosphere
Chemical characteristics and source apportionment of aerosols over Indian Ocean during INDOEX-1999
During INDOEX IFP-99, the samples of aerosols were collected onboard ORV Sagar Kanya over Indian Ocean along the cruise track, for chemical characterization and identification of dominating sources of aerosols. The concentrations of nss-SO4, nss-Ca, nss-Mg, NO3, K, NH4 and SO2 were observed to be significantly higher before ITCZ in northern hemisphere than across ITCZ in southern hemisphere. In this study, variation of concentrations of nss-SO4, nss-Ca and nss-K with respect to change in latitude, wind direction, wind speed and relative humidity have been highlighted. North of ITCZ, nss-SO4 varied from 2.20 to 18.31 μg/m3 and south of ITCZ from 0.50 to 2.79 μg/m3 while nss-Ca varied from 0.02 to 0.72 μg/m3 north of ITCZ and from 0.01 to 0.14 μg/m3 south of ITCZ. nss-K ranged 0.09-1.43 μg/m3 and 0.07-0.60 μg/m3 before ITCZ and across ITCZ respectively. nss-Ca and nss-SO4 were contributed mainly by NNW and ENE winds while nss-K was observed to be contributed mainly by SSW and ENE winds. Wind speed greater than 4.5 m/s negatively influenced the concentration of nss-Ca concentrations. Correlation coefficients of nss-SO4 with SO2 (r = 0.7) and RH (r = 0.5) suggested a significant contribution of nss-SO4 by aqueous phase oxidation of SO2. Using PCA, four major sources namely sea salt, biogenic combustion, secondary SO4 and crustal contribution were identified over Indian Ocean during INDOEX period
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
Several hundred genetic muscle diseases have been described, all of which are rare. Their clinical and genetic heterogeneity means that a genetic diagnosis is challenging. We established an international consortium, MYO-SEQ, to aid the work-ups of muscle disease patients and to better understand disease etiology. Exome sequencing was applied to 1001 undiagnosed patients recruited from more than 40 neuromuscular disease referral centers; standardized phenotypic information was collected for each patient. Exomes were examined for variants in 429 genes associated with muscle conditions. We identified suspected pathogenic variants in 52% of patients across 87 genes. We detected 401 novel variants, 116 of which were recurrent. Variants in CAPN3, DYSF, ANO5, DMD, RYR1, TTN, COL6A2, and SGCA collectively accounted for over half of the solved cases; while variants in newer disease genes, such as BVES and POGLUT1, were also found. The remaining well-characterized unsolved patients (48%) need further investigation. Using our unique infrastructure, we developed a pathway to expedite muscle disease diagnoses. Our data suggest that exome sequencing should be used for pathogenic variant detection in patients with suspected genetic muscle diseases, focusing first on the most common disease genes described here, and subsequently in rarer and newly characterized disease genes
The study of atmospheric ice-nucleating particles via microfluidically generated droplets
Ice-nucleating particles (INPs) play a significant role in the climate and hydrological cycle by triggering ice formation in supercooled clouds, thereby causing precipitation and affecting cloud lifetimes and their radiative properties. However, despite their importance, INP often comprise only 1 in 10³–10⁶ ambient particles, making it difficult to ascertain and predict their type, source, and concentration. The typical techniques for quantifying INP concentrations tend to be highly labour-intensive, suffer from poor time resolution, or are limited in sensitivity to low concentrations. Here, we present the application of microfluidic devices to the study of atmospheric INPs via the simple and rapid production of monodisperse droplets and their subsequent freezing on a cold stage. This device offers the potential for the testing of INP concentrations in aqueous samples with high sensitivity and high counting statistics. Various INPs were tested for validation of the platform, including mineral dust and biological species, with results compared to literature values. We also describe a methodology for sampling atmospheric aerosol in a manner that minimises sampling biases and which is compatible with the microfluidic device. We present results for INP concentrations in air sampled during two field campaigns: (1) from a rural location in the UK and (2) during the UK’s annual Bonfire Night festival. These initial results will provide a route for deployment of the microfluidic platform for the study and quantification of INPs in upcoming field campaigns around the globe, while providing a benchmark for future lab-on-a-chip-based INP studies
Rural versus urban gaseous inorganic reactive nitrogen in the Indo-Gangetic plains (IGP) of India
The present study reports on the abundance of reactive nitrogen (NH _3 and NO _2 ) at two sites, i.e. Okhla (urban site) in Delhi and Mai (rural site), located in the nearby state: Uttar Pradesh. The measurements were carried out during the period from October, 2012 to September, 2013 on a monthly basis. The average concentrations of NH _3 at Okhla and Mai have been recorded as 40.4 ± 16.8 and 51.57 ± 22.8 μ g m ^−3 , respectively. The average concentrations of NO _2 have been recorded as 24.4 ± 13.5 and 18.8 ± 12.6 μ g m ^−3 at Okhla and Mai, respectively. Results show that the seasonal variation at Mai was more prominent where NH _3 concentrations varied at 72.0 μ g m ^−3 during the winter, 47.2 μ g m ^−3 during the summer and 30.7 μ g m ^−3 during the monsoon season, whereas at Okhla the average NH _3 concentrations were almost equal during different seasons, namely 44.2 μ g m ^−3 during the winter, 42.5 μ g m ^−3 during the summer and 38.9 μ g m ^−3 during the monsoon season. This is probably due to significant differences in crops and in the fertilizer amounts applied across the seasons in rural areas, while urban areas have almost constant sources throughout the year. Winter concentrations were highest at both sites, followed by summer and then the monsoon season. The average NO _2 concentrations were recorded as 39.6 μ g m ^−3 , 24.5 μ g m ^−3 and 10.4 μ g m ^−3 during the winter, summer and monsoon season at Okhla, whereas the average NO _2 concentrations were recorded as 27.5 μ g m ^−3 , 17.2 μ g m ^−3 and 4.1 μ g m ^−3 during the winter, summer and monsoon season, respectively. NO _2 emissions at Okhla may be attributed to various urban activities, such as vehicular traffic and industries, while NO _2 emissions at Mai may be attributed to biomass burning as a major source. However, NO _2 concentrations from vehicular traffic and nearby industries cannot be ignored at Mai
Real-time wet scavenging of major chemical constituents of aerosols and role of rain intensity in Indian region
Real-time simultaneous studies on chemical characteristics of rainwater and PM10 aerosols were carried out to understand the scavenging of major chemical components in Indian region. The concentrations of Ca2+, NH4+, SO42− and NO3− were observed to be lower in the aerosol samples collected during rain as compared to before and after rain events. The most significant reduction was noticed for Ca2+ (74%) during rain which showed highest scavenging ratio (SR) and indicated that below-cloud scavenging is an effective removal process for Ca2+ in Indian region. Among non-sea salt components, Ca2+ had highest SR at Hyderabad indicating typical characteristics of crustal influence as abundance of calcium carbonate in soil dust has been reported in India. However, the levels of these major chemical components gradually got build-up in due course of time. After rain events, the levels of SO42− aerosols were noticed to be substantially higher (more than double) within 24 h. In general, scavenging ratios for all components (except Ca2+, NH4+ and K+) were higher over BOB as compared to Hyderabad. The maximum fall in aerosol levels (BR minus AR) was observed during continuous and low intensity rain events that did not allow building up of aerosol concentrations
GHG AND AEROSOL EMISSION FROM FIRE PIXEL DURING CROP RESIDUE BURNING UNDER RICE AND WHEAT CROPPING SYSTEMS IN NORTH-WEST INDIA
Emission of smoke and aerosol from open field burning of crop residue is a long-standing subject matter of atmospheric pollution. In this study, we proposed a new approach of estimating fuel load in the fire pixels and corresponding emissions of selected GHGs and aerosols i.e. CO2, CO, NO2, SO2, and total particulate matter (TPM) due to burning of crop residue under rice and wheat cropping systems in Punjab in north-west India from 2002 to 2012. In contrasts to the conventional method that uses RPR ratio to estimate the biomass, fuel load in the fire pixels was estimated as a function of enhanced vegetation index (EVI). MODIS fire products were used to detect the fire pixels during harvesting seasons of rice and wheat. Based on the field measurements, fuel load in the fire pixels were modelled as a function of average EVI using second order polynomial regression. Average EVI for rice and wheat crops that were extracted through Fourier transformation were computed from MODIS time series 16 day EVI composites. About 23 % of net shown area (NSA) during rice and 11 % during wheat harvesting seasons are affected by field burning. The computed average fuel loads are 11.32 t/ha (±17.4) during rice and 10.89 t/ha (±8.7) during wheat harvesting seasons. Calculated average total emissions of CO2, CO, NO2, SO2 and TPM were 8108.41, 657.85, 8.10, 4.10, and 133.21 Gg during rice straw burning and 6896.85, 625.09, 1.42, 1.77, and 57.55 Gg during wheat burning. Comparison of estimated values shows better agreement with the previous concurrent estimations. The method, however, shows its efficiency parallel to the conventional method of estimation of fuel load and related pollutant emissions
Separation and determination of 3,4-dimethoxybenzaldehyde and related compounds by high performance capillary electrophoresis
662-6653,4-Dimethoxybenzaldehyde and five
related compounds have been separated and determined by high performance
capillary electrophoresis using micellar electrokinetic chromatography method.
Good separation for all the compounds is achieved using 10 mM di-sodium
tetraborate, 100 mM sodium dodecyl sulphate and 10% acetonitrile. The
detection has been carried out at 214 nm using UV-vis detector. The proposed
method has been further applied for the quality control of two commercial
samples
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