Spatial and temporal variations in the atmospheric concentrations of "Stockholm Convention" organochlorine pesticides in Kuwait.

The study reports fortnightly atmospheric concentrations of organochlorine pesticides concomitantly measured at an urban, "industrial" and a remote location over a twelve month period in Kuwait to examine seasonal variability and urban-rural concentration gradients. The average±SD (and range) of the ΣOC concentrations measured throughout the study period in decreasing order were urban, 505±305 (range, 33-1352) pgm-3, remote, 204±124 (4.5-556) pgm-3, and "industrial" 155±103 (8.8-533) pgm-3. The concentrations of most OCs measured in this study, except for DDT and its metabolites, were higher at urban locations relative to their concentrations at remote location, in line with the literature on POPs regarding urban conurbations being sources of industrial chemicals. The most abundant pesticides measured throughout this study were dieldrin, pentachlorobenzene, hexachlorobenzene, ΣDDTs, ΣHCHs, and oxychlordane. Hexachlorobenzene concentrations were generally higher than those of pentachlorobenzene and are both strongly negatively correlated with temperature (p<0.05) at all sampling locations. Mean summertime concentrations were higher for hexachlorocyclohexanes, chlordanes, dieldrin, and DDT isomers, except for pp-DDT. This may suggest that concentrations of these compounds may be driven by temperature.

Seasonal variations in the atmospheric concentrations of polychlorinated biphenyls in Kuwait.

The spatial and temporal variations in the atmospheric concentrations of PCBs were concomitantly measured at several sites over a twelve-month period in Kuwait to examine seasonal variability and urban-rural concentration gradients using two sampling methods. The annual mean (and range) of ∑PCB concentrations measured using high volume samplers was 10.8 (1.2-32) pg m-3 at the remote site and 39.4 (1.1-128) pg m-3 at the urban site. The median concentrations of ΣPCBs at the urban location (30.3 pg m-3) was significantly higher (p < 0.001) than that measured at the remote location (8.6 pg m-3) consistent with the view that urban centers are an important net source of these compounds to the environment. Passive sampler derived concentrations across the country showed a uniform distribution except at a few locations in the vicinity of suspected sources where elevated concentrations were measured. As with active sampling data, the concentrations measured using passive samplers were higher in urban areas (range, 4-78 pg/m3) compared to remote sites (range, 2.2-17 pg/m3). The concentrations measured at some urban sites correlated extremely well with mean temperature during the deployment period whereas temperature correlations with measured concentrations were negative at remote and semi-rural sites suggesting that air-surface exchange maybe a key driving mechanism of the current levels of PCBs in Kuwait.

Depositional time trends of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in a dated sediment core from the Northern Arabian Gulf.

The historical record of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) deposition was reconstructed from the analysis of a dated sediment core collected from a remote area in the northwestern Arabian Gulf not influenced by any point sources of contamination. The sedimentary record showed that PCDD/F concentrations started to increase above pre-industrial background levels in the mid-1960s. This was followed by an exponential increase in concentrations attaining a maximum of 7.5pg/g (dry wt) in the early 1980s and stayed fairly constant thereafter. The homolog profiles in sediments remained fairly consistent throughout the core with PCDD contributing 75% of the ΣPCDD/F concentrations. The homolog profile was dominated by OCDD which contributed approximately 55% of the total dioxins throughout the core. The consistency in the homolog patterns throughout the core suggests that the source of dioxins have remained fairly unchanged throughout the sedimentary record represented by the core.

Spatial and temporal distributions of polycyclic aromatic hydrocarbons in the Northern Arabian Gulf sediments.

Surficial sediment samples were collected from 25 locations within Kuwait Bay and outside the Bay, in the Northwestern Arabian Gulf, to access recent polycyclic aromatic hydrocarbon pollution in Kuwait. Time trends in the depositional history of PAHs to this portion of the Arabian Gulf was reconstructed from the analysis of a dated sediment core. Intersite differences in concentration exist although these differences were not statistically significant (p=0.08). However, organic carbon normalized concentrations within Kuwait Bay were 4 times higher than the average concentrations outside the Bay and were shown to be statistically significant (p<0.001). The sedimentary record showed that ΣPAHs concentration fluctuated between 12 and 25ngg-1 before 1970. Concentrations then increased sharply to a maximum of 45ngg-1 around the late 1970s and early 1980s followed by an exponential decrease in concentration to pre-1970 "background" concentrations of between 12 and 25ngg-1.

Polybrominated diphenyl ether concentrations in sediments from the Northern Arabian Gulf: spatial and temporal trends.

Surficial sediment samples were obtained from 25 locations within Kuwait Bay and outside the Bay, in the Northwestern Arabian Gulf, to access recent pollution in Kuwait. The historical deposition of PBDEs to this portion of the Arabian Gulf was reconstructed by collecting a sediment core at the entrance of Kuwait Bay. The mean (and range) in concentrations of ∑11PBDEs in surficial sediments was 0.164±0.09 (0.06-0.44) pg/g dw. The concentrations measured in Kuwait Bay were generally higher than those measured in the open Gulf. When the concentrations were normalized to organic carbon, the average ∑11PBDEs concentrations measured in Kuwait Bay were seven times higher than average concentrations outside the Bay. The historical record, reconstructed from a sediment core collected at the entrance of Kuwait Bay, showed that Σ11PBDE concentrations were generally low in deeper sediment sections. The concentrations started to increase above background in the mid-1950s and increased sharply to a maximum Σ11PBDE concentration of ca 1,100 pg/g in the late 1980s. Concentrations decreased thereafter until another pulse in concentrations was observed around the early 2000 followed by a decrease in subsequent years. It is likely that the initial pulse in concentration recorded in sediments is related to inputs from the Gulf war of 1991. The penta congeners were observed throughout the length of the core although the concentrations were low. The congeners present in the Deca-PBDE technical mixture, particularly BDE 209 which is the main congener in the Deca-BDE mixture, occurred in sediment cores around the 1980s, and the concentrations increased rapidly thereafter being the most dominant congener since their first detection in sediments. The presence of nona-BDE congeners in proportions exceeding those in commercial mixtures may be suggestive of debromination of BDE 209 in sediments.

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.

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.

Polybrominated diphenyl ethers (PBDEs) in soils along a rural-urban-rural transect: sources, concentration gradients, and profiles.

This study reports concentrations of PBDEs in surface soil samples collected along a 140 km transect across Kuwait to assess the role of urban centers as sources of persistent organic pollutants to the surrounding environment. The ΣPBDE concentrations varied by a factor of ~250 and ranged from 289 to 80,078 pgg (-1)d.w. The concentrations of PBDEs in Kuwait City were significantly higher (p<0.01) than those collected from sites outside the city supporting the hypothesis that urban centers are sources of PBDEs. The congener profiles were dominated by BDE-209, accounting for 93% of the PBDEs in the soil samples. The concentrations of all congeners (except BDE-209) were highly correlated with percent organic carbon (%OC) (p>0.05) when the data from Kuwait City was omitted from the analysis. These findings suggest that soil concentrations outside the urban centers were close to equilibrium with the atmosphere.

Polybrominated diphenyl ethers in three commercially important fish from the northwestern Arabian Gulf: occurrence, concentration, and profiles.

Polybrominated diphenyl ethers (PBDEs) were measured in three species of fish (yellowfin seabream [Acanthopagrus latus, a predatory fish]; Klunzinger's mullet [Liza klunzingeri, a pelagic fish]; and large-scaled tonguesole [Cynoglossus arel, a demersal fish]) collected from two sites in the northwestern part of the Arabian Gulf, a marginal sea of the tropical Indo-Pacific Ocean. Concentrations of ΣPBDEs ranged from 11 to 57 ng g(-1) lipid weight (lw) for mullet, 5.0-38 ng g(-1) lw for tonguesole, and 2.8-48 ng g(-1) lw for seabream in Kuwait Bay, whereas in the open gulf, concentrations ranged from 6.0 to 160 lw for mullet, 8.3-190 lw for tonguesole, and 7.1-62 for lw for seabream. The congener composition in all species from both sites was dominated by BDEs 47, 99, and 100, which together constituted approximately 90% of the congeners detected. Although no statistically significant intersite differences were found, ΣPBDEs concentrations in mullet were significantly higher than those in seabream (p = 0.01). However, no significant differences existed between mullet and tonguesole (p = 0.28) or between tonguesole and seabream (p = 0.06). ΣPBDE concentrations were negatively correlated with fish mass for all species; however, the correlations were statistically insignificant, suggesting a growth dilution effect.

Polycyclic aromatic hydrocarbons in indoor air and dust in Kuwait: implications for sources and nondietary human exposure.

This study reports concentration of polycyclic aromatic hydrocarbons (PAHs) in indoor air and dust samples collected from 24 homes in Kuwait. Mean SigmaPAHs in indoor air ranged from 1.3 to 16 ng/m(3) with a geometric mean of 5.6 ng/m(3), whereas the dust concentrations varied over three orders of magnitude, from 3 to 2920 ng/g, with a geometric mean of 165 ng/g. The low-molecular-weight tricyclic and tetracyclic PAHs dominated the air profile constituting approximately 70-90 % of the measured compounds, with phenanthrene (51%), fluorene (13 %), fluoranthere (8 %), and pyrene (7 %) being the major contributors. The PAH profile in dust was dominated by the high-molecular-weight PAHs, with three compounds (benzo[a]pyrene, benzo[k]fluoranthene, and benzo[b]fluoranthene) contributing approximately 60% of the average SigmaPAHs measured in the samples. Indoor-to-outdoor (I/O) ratios for individual compounds were <1 for the majority of compounds, suggesting that there were no significant indoor sources for these compounds in these homes. Using the measured concentrations in air and dust, together with estimates of inhalation and inadvertent dust ingestion rates for children and adults, estimated human nondietary exposure on a BaP(equiv) basis were 547 pg/kg body weight/day and 205 pg/kg body weight/day for children and adults, respectively. Exposure from dust ingestion contributes about 42% of nondietary intake of SigmaPAHs in children, but only 11% for adults. The threefold 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.

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.