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[Display omitted] • Measurement of GEM emissions from urban atmosphere in Pakistan. • Open burning, and physical dismantling are common e-waste recycling practices. • E-waste sites from Karachi, Lahore, and Peshawar were found highly contaminated. • Lower seasonal variations indicating the stable emission sources throughout year. • Workers and public living close to these facilities are exposed to hazards of GEM. Detrimental effects of mercury (Hg) on ecosystems and human health have been well-documented. Whereas emissions of gaseous elemental mercury (GEM) from e-waste recycling have been reported in developed countries, much less is known about the situation in the Global South. Using a total of 132 passive air samplers, seasonally resolved concentrations of GEM in air were measured continuously at 32 informal e-waste recycling facilities and background location in Pakistan for a period of one year between September 2020 and December 2021. Annual average GEM concentrations at the studied locations ranged from 1.8 to 92 ng m−3. Among the studied cities, higher concentrations were measured in Karachi (mean ± s.d: 17 ± 22, range: 4.2–92 ng m−3), Lahore (16 ± 4.2, 8.2–22 ng m−3) and Peshawar (15 ± 17, 4.9–80 ng m−3), while lower levels were measured in Hyderabad (6.9 ± 6.2, 3.1–25 ng m−3), consistent with a higher rate of informal recycling activities in metropolitan areas. Seasonally, higher GEM levels occurred during autumn (15 ± 16: 3.3–92 ng m−3) and summer (13 ± 8.7: 1.8–80 ng m−3) than in winter (12 ± 8.4: 2.5–49 ng m−3) and spring (9.2 ± 7.3: 1.8–80 ng m−3), possibly reflecting enhanced volatilization at higher temperatures and/or varying magnitude of recycling operations in different seasons. Policies and strict regulations related to e-waste management should be developed and implemented urgently in the country. [ABSTRACT FROM AUTHOR]

Samples of airborne particulate matter (PM2.5) were collected at a site in Lahore, Pakistan from November 2005 to January 2006. A total of 129 samples were collected using an Andersen Reference Ambient Air Sampler 2.5-400 sampler and analyzed for major ions, trace metals, and organic and elemental carbon concentrations. The data set was then analyzed by positive matrix factorization (PMF) to identify the possible sources of the atmospheric PM collected in this urban area. Six factors reproduced the PM2.5 sample compositions with meaningful physical interpretation of the resolved factors. The sources included secondary PM, diesel emissions, biomass burning, coal combustion, two-stroke vehicle exhaust, and industrial sources. Diesel and two-stroke vehicles contributed about 36%, biomass burning about 15%, and coal combustion sources around 13% of the PM2.5 mass. Nearly two thirds of the PM2.5 mass is carbonaceous material. Secondary particles contributed about 30% of PM2.5 mass. The conditional probability function (CPF) was then used to help identify likely locations of the sources present in this area. CPF analysis point to the east and northeast, which are directions of urban and industrial areas located across the border near Amritsar, India as the most probable source for high PM2.5 concentration from diesel and two-stroke vehicles exhaust in Lahore. Analysis of those days within three different ranges of PM2.5 concentration shows that most of the measured high PM2.5 mass concentrations were driven by diesel and two-stroke vehicle emissions including the associated primary sulfate. The use of the potential source contribution function (PSCF) to find the source locations of regionally transported particles is inapplicable in situations when high PM2.5 concentrations are dominated by local sources and local meteorology. [ABSTRACT FROM AUTHOR]

The article presents a study which measured the concentration of 7beryllium (Be) in the outdoor ambient air of Lahore City in Pakistan. The concentration of the cosmogenic radionuclide was measured using two air samplers and a high purity germanium detector. The air samplers were used in collecting samples of air particulates. The study has found that 7Be concentration exists in the range from 1.6 to 11.3 megabecquerel per cubic metre. Rainfall reduces the concentration of the cosmogenic radionuclide in outdoor air.

The emission of polychlorinated biphenyls (PCBs) in South Asian countries is one of the great environmental concerns and has resulted in the contamination of surrounding high altitude regions such as Azad Jammu and Kashmir (AJK), Pakistan. This first investigation of Polychlorinated Biphenyl (PCBs) concentrations in the ambient air, water and surface soil was conducted along the extensive stream network in the AJK valley of the Himalayan Region. In 2014, surface soil samples were taken and passive air and water samplers were deployed along the four main rivers, namely Jhelum, Neelum, Poonch and Kunhar, and analysed for PCBs (33 congeners) using GC-MS/MS. The ∑ 33 PCBs concentrations ranged from 31.17 to 175.2 (mean ± SD: 81 ± 46.4 pg/L), ND to 1908 (1054 ± 588.5 pg/g), and 29.8 to 94.4 (52.9 ± 22.7 pg/m3) in surface water, soil and air matrices, respectively. The levels of dioxin-like PCBs (∑ 8 DL-PCBs) contributed considerably towards the total PCBs concentrations: 60.63% (water), 43.87% (air) and 13.76% (soil). The log transformed air-water fugacity (log fa/fw) ratios ranged from −9.37 to 2.58; with 86.3% of the sampling sites showing net volatilization of selected PCB congeners. Similarly, the fugacity fractions for air-soil exchange exhibited narrow variation (0.8 to < 1) indicating net volatilization of PCBs. The ecological risk assessment showed low potential ecological risks ( E r i = 1.58–7.63) associated with PCB contamination. The present findings provide baseline data that suggest cold trapping of POPs in the remote mountainous areas of Pakistan and can support environmental management of POPs at the regional level. This pioneer investigation campaign to assess the PCBs concentrations in Himalayan Riverine Network of Azad Jammu and Kashmir, Pakistan helps to develop baseline data of PCBs from the strategically important riverine environment that would help in future regional as well as global ecological studies. However, the effects of temperature variations on the sampling rates of chemicals across a wide spectrum of volatility along the elevation gradient were not taken under consideration for PCBs atmospheric concentrations. Image 1 • Pioneer investigation of PCBs in riverine network of AJK, Pakistan. • Hepta-PCBs (in water), penta-PCBs (in soil), and hexa-PCBs (in air) identified as dominant homologs. • Net volatilization of PCBs from soil and water to the atmosphere. • Low potential ecological risks associated with PCB contamination. Practical Implications: [ABSTRACT FROM AUTHOR]