Polycyclic aromatic hydrocarbons (PAHs) in indoor dust samples from Cities of Jeddah and Kuwait: Levels, sources and non-dietary human exposure.

This study reports levels and profiles of polycyclic aromatic hydrocarbons (PAHs) in dust samples collected from three different microenvironments (cars, air conditioner (AC) filters and household floor dust) of Jeddah, Saudi Arabia (KSA) and Kuwait. To the best of our knowledge, this is first study reporting PAHs in indoor microenvironments of KSA, which makes these findings important. Benzo(b)fluoranthene (BbF), benzo(a)pyrene (BaP), phenanthrene (Phe), and pyrene (Pyr) were found to be the major chemicals in dust samples from all selected microenvironments. ΣPAHs occurred at median concentrations (ng/g) of 3450, 2200, and 2650 in Saudi AC filter, car and household floor dust, respectively. The median levels (ng/g) of ΣPAHs in Kuwaiti car (950) and household floor (1675) dust samples were lower than Saudi dust. The PAHs profile in Saudi dust was dominated by high molecular weight (HMW) (4-5 ring) PAHs while in Kuwaiti dust 3 ring PAHs have marked contribution. BaP equivalent, a marker for carcinogenic PAHs, was high in Saudi household floor and AC filter dust with median levels (ng/g) of 370 and 455, respectively. Different exposure scenarios, using 5th percentile, median, mean, and 95th percentile levels, were estimated for adults and toddlers. For Saudi and Kuwaiti toddlers worst exposure scenario of ΣPAHs was calculated at 175 and 85ng/kg body weight/day (ng/kgbw/d), respectively. For Saudi toddlers, the calculated worst exposure scenarios for carcinogenic BaP (27.7) and BbF (29.3ng/kgbw/d) was 2-4 times higher than Kuwaiti toddlers. This study is based on small number of samples which necessitate more detailed studies for better understanding of dynamics of PAHs in the indoor environments of this region. Nevertheless, our finding supports the ongoing exposure of organic pollutants to population that accumulates indoor.

Organohalogenated contaminants in sediments and bivalves from the Northern Arabian Gulf.

Several classes of Organohalogenated contaminants (OHCs) were determined in sediments and bivalves collected from Kuwait coast. The levels and profile of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs) and polybrominated diphenyl ethers (PBDEs) were compared in both sediments and bivalves. PCB-153 and -138 were the major contributors towards total OHCs followed by DDT and its metabolites (DDTs). The higher contribution of DDTs (~40%) and BDE-47 (~15%) in bivalves as compared to that in associated sediments indicated high biota-sediment accumulation factors (BSAF). Higher BSAF (values for heavier PCBs, DDTs and PBDEs) also indicated their high accumulation potential from sediment into associated biota at most of the studied locations. Overall, OHCs in sediments and bivalves measured in current study were lower than those reported in the literature worldwide. Most of the sediment concentrations of OHCs (ng/g, dry weight) were in the range of permissible guideline values proposed by Canadian Sediment Quality Guidelines (CSQGs), with few exceptions for DDTs (5 ng/g) and PCBs (22.7 ng/g). Similarly, 10% of bivalve samples contained high levels (ng/g, lipid weight) of PCBs (300) and DDTs (150) and were above the set safety benchmarks. This study establishes baseline for future monitoring programs.

Seasonal variations in the atmospheric concentrations of polybrominated diphenyl ethers in Kuwait.

The study reports fortnightly atmospheric concentrations of PBDEs concomitantly measured at an urban and a remote location over a twelve-month period in Kuwait to examine seasonal variability and urban-rural concentration gradients. The annual mean (and range) of ∑PBDE concentrations was 32 (3-208) pgm(-3) at the remote site and 57 (0.3-445) pgm(-3) at the urban site. Although not statistically significant, the median (29 pg m(-3)) and mean (57 pg m(-3)) concentrations at the urban location were higher than those measured at the remote location (18 and 29 pg m(-3) respectively), consistent with the view that urban centers are an important net source of these compounds to the environment. Although Clausius-Clapeyron plots showed statistically significant correlations (p<0.05) with temperature for low molecular weight congeners (BDEs 28, 47, 100), correlations with the ΣPBDE concentrations were not significant at both urban and remote sites. The seasonal variations in ΣPBDE concentrations were not markedly different at the urban location, but the median summer ΣPBDE concentration at the remote location was significantly higher than winter median ΣPBDE concentrations. The absence in seasonality at the urban location may be due to ongoing primary emissions in urban areas.

Levels and profiles of organochlorines and flame retardants in car and house dust from Kuwait and Pakistan: implication for human exposure via dust ingestion.

There are only few studies documenting indoor pollution in the Middle East and the Indian subcontinent. In present study, we have evaluated the occurrence of various organochlorines (OCs) and flame retardants (FRs) in dust from cars and houses of Pakistan and Kuwait. Polybrominated diphenyl ethers (PBDEs), novel brominated flame retardants (NBFRs), organophosphate FRs (PFRs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs) were investigated in indoor dust from urban houses (N=15 per country) and cars (N=15 per country). PFRs were the major analytes in all four microenvironments, followed by PBDEs>NBFRs>OCPs>PCBs. For all classes of analytes, relatively lower levels were observed in car and house dust from Pakistan than Kuwait. Levels of ∑PBDEs, ∑NBFRs and ∑PFRs were higher in car dust, while ∑OCPs and ∑PCBs were higher in house dust from both countries. ∑PFRs occurred at average concentrations of 16,900, 87,900, 475, and 2500ng/g in Kuwaiti house and car, and Pakistani house and car dust, respectively. For both countries, the profiles of analytes in car dust were different from those in the house dust. Different exposure scenarios using 5th percentile, median, mean, and 95th percentile levels were estimated for adult, taxi drivers and toddlers. For Kuwaiti toddlers, assuming high dust intake and mean and 95th percentile concentrations, the values computed for ∑OCPs (1500ng/kg bw/day) were higher than RfD values, while for ∑PCBs (14.5ng/kg bw/day) it was only two-fold lower than the corresponding RfDs.

Effect of environmental factors on photodegradation of polycyclic aromatic hydrocarbons (PAHs) in the water-soluble fraction of Kuwait crude oil in seawater.

Photodegradation of PAHs in the water-soluble fraction of Kuwait crude oil in seawater was investigated under various environmental factors (temperature, light intensity, oxygen levels and presence of a sensitizer) in laboratory conditions. All factors investigated had significant effect on the degradation rates of PAHs. At 15 °C almost all PAHs optimally degraded at an oxygen level of 4 ppm. For lower molecular weight PAHs a light intensity of 500 W/m(2) in the presence of the sensitizer worked well. Higher molecular weight PAHs degraded at faster rates at a light intensity 750 W/m(2). At 30 °C, most of the PAHs degraded optimally at an oxygen level of 0 ppm and light intensity of 500 or 750 W/m(2) in presence of the sensitizer. At 40 °C, most of PAHs degraded optimally at low oxygen concentrations (0 and 4 ppm) and a light intensity of 500 W/m(2) in the presence of the sensitizer. Linear regression indicated that for most of the compounds, light intensity had the greatest effect on degradation rates.

Passive sampler-derived air concentrations for polybrominated diphenyl ethers and polycyclic aromatic hydrocarbons in Kuwait.

The present study presents, to our knowledge, the first ambient air data for a range of polybrominated diphenyl ethers (PBDEs) and polycyclic aromatic hydrocarbons (PAHs) in Kuwait. This was achieved by concurrently deploying polyurethane foam-disk passive samplers at 14 sites over a six-week period. Calculated mean sigma5PBDE concentrations (sum of brominated diphenyl ethers [BDEs] 47, 99, 100, 153, and 154) ranged from 2.5 to 32 pg/m3 of air, with BDE 47 contributing between 39 and 65% of the sigmaPBDEs detected. Differences in relative concentrations were observed between sites, with higher concentrations measured close to suspected sources. Calculated sigmaPAH concentrations ranged from 5 to 13 ng/m3 (mean, 8.3 ng/m3). The compound distribution was dominated by three- and four-ring compounds, which constituted approximately 90% of the sigmaPAHs, with phenanthrene contributing approximately 35%. However, the proportion of five- and six-ring PAHs increased around the "oil lakes," which were formed by the torching of oil wells during the 1991 Gulf War. The oil lakes are a reservoir of PAHs that will continue feeding the atmosphere as long as they remain untreated.

House dust as a source of human exposure to polybrominated diphenyl ethers in Kuwait.

This study reports concentrations of polybrominated diphenyl ethers (PBDEs) in dust samples collected from 17 homes in Kuwait. PBDEs were measured in all homes investigated with mean summation operatorPBDEs concentration ranging from 1 to 393 ng g(-1), with a geometric mean of 76 ng g(-1). The dominant congener in all samples was BDE 209 constituting ca. 85% of the summationPBDEs followed by BDE 99 (5%), BDE 47 (4.5%), and BDE 183 (2%). The congener mixture in dust is dominated by those in deca and penta formulations. Using the measured concentrations and estimates of dust ingestion rates for children and adults, estimated human non-dietary exposure based on mean PBDE levels were 14.8 and 1.5 ng day(-1) for children and adults, respectively. The 10-fold difference in exposure estimates between children and adults in this study supports previous reports that children are at greater risk from pollutants that accumulate indoors. The ubiquitous distribution of these chemicals as noted in this study highlights the fact that we are continuously exposed to low doses of chemicals in the indoor environment.