Antibiotics in Wastewater: Baseline of the Influent and Effluent Streams in Kuwait.

This study provides baseline information on the concentrations of antibiotics in influent and effluent from two wastewater treatment plants in regular operation in the State of Kuwait. Wastewater samples were collected from the influent and effluent streams of two WWTPs, over four sampling campaigns and analyzed for a broad range of antibiotics. The mean influent concentrations of sulfamethoxazole, ciprofloxacin, clarithromycin, and cefalexin were 852 ng/L, 672 ng/L, 592 ng/L), and 491 ng/L, respectively, at Umm Al Hayman WWTP. At the Kabd WWTP, the influent concentration of clarithromycin was highest with a mean of 949 ng/L, followed by ciprofloxacin (mean, 865 ng/L), cefalexin (mean, 598 ng/L), and sulfamethoxazole (mean, 520 ng/L). The dominant compounds in the effluent from Umm Al Hayman were sulfamethoxazole (mean, 212 ng/L), ciprofloxacin (mean, 153 ng/L), ofloxacin (mean, 120 ng/L), dimetridazole (mean, 96 ng/L), and metronidazole (mean, 93 ng/L). Whereas, at the Kabd WWTP, the dominant compounds were sulfamethoxazole (mean, 338 ng/L), dimetridazole (mean, 274 ng/L), cefalexin (mean, 213 ng/L), ciprofloxacin (mean, 192 ng/L), and clarithromycin (189 ng/L). The mean influent concentrations of all compounds were higher than those measured in the effluents. The concentrations of antibiotic compounds were not significantly different between the two WWTPs (p > 0.05). The removal efficiencies of the various antibiotics over the four sampling campaigns for the Kabd and Umm Hayman WWTPs ranged between 10.87 and 99.75% and also showed that they were variable and were compound dependent. The data clearly show that the concentrations of antibiotics measured in the influents of both WWTPs were highest in samples collected during the winter-summer (September samples) transition followed by the concentrations measured during the winter-summer (March samples) transition period. This is possibly linked to the increased prescription of these medications to treat infectious diseases and flu prevalent in Kuwait during these periods. This study provides the first reported concentrations of antibiotics in the dissolved aqueous influents and effluents of WWTPs in Kuwait. Additional studies are required to evaluate the environmental impact that antibiotic residues may cause since treated wastewater is used in irrigation, and often there are instances when untreated wastewater is discharged directly into the marine environment.

Temporal trend of polychlorinated biphenyls contamination in the northwestern Arabian Gulf - Evidence from sediment records.

This study provides an insight into the polychlorinated biphenyls (PCBs) inventories in the sediments of the northwestern Arabian/Persian Gulf. PCBs can be used as chemical markers that correlate with historical events in the region, to estimate the sedimentation rates in the northern Gulf, and to determine the sources of pollutants in the study area. The concentrations of PCBs were generally patchy in sediments. At Station 1 the ΣPCB concentrations generally fluctuated between 0.100 and 0.400 ng g-1 dw throughout the depositional history measured in a sediment core. There were four peaks in the ΣPCB profile corresponding to 1969, 1979, 1983 and 1991. Station 2 showed a prominent peak at depth of 25 cm. The concentrations of the ΣPCBs and ΣICE congeners at this depth were 28 and 12 ng g-1 dw respectively. Concentrations then dropped dramatically thereafter by a factor of 4. The ΣPCB concentrations at Station 3 were very low compared to the concentrations measured at Stations 1 and 2. The PCB concentration in Core 4 which was taken from open waters was 2-3 orders of magnitude lower than those in the other coastal cores. However, a 1990-91 peak was omnipresent in these cores. There is no record of PCB production within the Gulf region, and PCB releases into the Kuwait marine environment are likely to originate from their use in products. These maxima in early-1990s can be correlated to inputs from war-related activities, including the reported destruction of PCB-containing transformers and military equipment during the occupation of Kuwait. None of the recent sediment core sections at the four stations had a ΣPCB concentration near the effects range-median (ERM) concentration of 180 ng g-1, or permissible exposure limits (PEL) of 189 ng g-1, or were above the effect range-low (ERL) values of 22.7 ng g-1.

Baseline concentrations of pharmaceuticals in Kuwait's coastal marine environment.

This study was carried out to provide baseline information on the concentrations of pharmaceuticals in Kuwait's coastal waters. Samples were collected over four sampling campaigns from various outfalls that occasionally discharged water into the marine environment and analyzed for a range of pharmaceuticals including analgesic/anti-inflammatories, antibiotics, anticoagulant, antidiabetic, antihelmintics, antihypertensives, antiplatelet agent, asthma medication, ß-blocking agent, calcium channel blocker, diuretic, histamine H1 and H2 receptor antagonist, lipid regulators/cholesterol-lowering, prostatic hyperplasia, psychiatric drug, sedation and muscle relaxant, synthetic glucocorticoid, tranquilizer and x-ray contrast media. The levels varied between the detection limits of the method and a maximum of 28,183 ng/L for analgesics/anti-inflammatories. The highest pharmaceutical concentrations were in samples collected during the September campaign, possibly linked to the increased prescription of these medications to treat infectious diseases and flu prevalent in Kuwait during the winter months. The spatial variation is concentration is evident with KISR site being most polluted as hospital wastewater is discharged at the site. This study provides the first dataset on the concentrations of pharmaceuticals in the seawater in Kuwait and possibly the wider Arabian Gulf. Kuwait's coastal water pharmaceutical concentrations derived from this study exceed those reported from the Spanish coast, the Hong Kong harbour, the Bohai and the Yellow seas. More studies are needed to evaluate the environmental impact that these residues may have on non-target organisms.

Depositional time trends of phosphorous accumulation in a dated sediment core from the northwestern Arabian Gulf: Can phosphorous be used to support 210Pb chronologies in coastal aquatic sediments?

The use of 210Pb dating for the reconstruction of contaminant profiles in undisturbed sediments is the most widely acceptable technique historically. Due to the uncertainties associated with the technique, dating of sediments have often been supported by ancillary evidence such as an alternative historical marker in the catchment that is preserved in the sedimentary records. The most widely used verification marker is 137Cs, which is attributed to global fallout from past nuclear weapons testing, and the Chernobyl accident. In the southern hemisphere, and the mid-latitudes, the 137Cs signal from Chernobyl fallout is often absent from the sedimentary records making it very difficult to verify the 210Pb chronologies in these natural archives. This study reports the spatial and temporal variability of total phosphorus (TP) and its forms in sediments from Kuwait Bay and provides evidence of the possibility of using Phosphorous as a potential marker to support dates derived from 210Pb dating. In the current study we report the spatial and temporal variations in the concentrations of Phosphorus from near-shore sediments from Kuwait. The mean (and range) of TP concentration in surficial sediments is 19.4 (12.2 to 24) µmol-P g-1 dry weight. The highest concentrations were measured in the deepest portions of the Bay which is characterized by fine grained sediments. The vertical profile of TP in the sediments was characterized by a gradual increase in concentration from lower layers to a subsurface maximum (at approximately 4-5 cm) followed by an exponential decrease to the sediment-water interface. The sedimentary TP profile correlated remarkably well with changes in the population of Kuwait over the last three decades, suggesting that wastewater inputs into the Bay from treatment plants are an important source of phosphorus in the coastal waters. The decrease in concentration in sediment deposited over the last five years of the core is explained by the commissioning of an improved wastewater treatment plant with higher phosphorus removal efficiency. These fluctuations preserved in the sedimentary records linked to identifiable historical events provides powerful evidence that this nutrient associated with wastewater inputs in coastal aquatic environments can be used as ancillary information to support 210Pb dating.

Organophosphate esters in indoor dust from 12 countries: Concentrations, composition profiles, and human exposure.

A total of 20 organophosphate triesters (OPEs), including seven alkyl-OPEs, three chlorinated (Cl)-OPEs, seven aryl-OPEs, and three oligomeric-OPEs were measured in 341 house dust samples collected from 12 countries during the period 2010-2014. OPEs were ubiquitous in indoor dust, and the total concentrations of OPEs (∑OPEs; sum of 20 OPEs) ranged from 49.4 to 249,000 ng/g dry weight (dw). Generally, Cl-OPEs were the predominant compounds (51% of total) in indoor dust samples, with a median concentration of 800 ng/g, followed by alkyl-OPEs (31%), aryl-OPEs (17%), and oligomeric-OPEs (1%), with median concentrations of 480, 270, and 21.9 ng/g, respectively. ∑OPE concentrations in indoor dust from more industrialized countries (South Korea: median, 31,300; Japan: 29,800; and the United States: 26,500 ng/g dw) were one or two orders of magnitude higher than those from less industrialized countries (Greece: 7140, Saudi Arabia: 5310, Kuwait: 4420, Romania: 4110, Vietnam: 1190, China: 1120, Colombia: 374, India: 276, and Pakistan: 138 ng/g dw). Statistically significant positive correlations (0.114 < r < 0.748, p < 0.05) were found among the concentrations of 16 OPEs in dust samples, indicating similar sources of these compounds. The median estimated daily intakes of ΣOPEs via dust ingestion for children and adults were in the ranges of 0.29-64.8 and 0.07-14.9 ng/kg bw/day, respectively.

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.

Atmospheric concentration of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (dl-PCBs) at Umm-Al-Aish oil field-Kuwait.

A sampling campaign was carried out to assess the impact of the oil field activities on the concentrations of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (dl-PCBs) in ambient air at Umm Al-Aish oil field in northern Kuwait. Sixteen samples were collected from March 2014 to January 2015. The concentrations of ΣPCDD/Fs were relatively high (33.6-586 fg I-TEQ/m3; median: 94.7 fg I-TEQ/m3; 31.2 to 516 fg WHO-TEQ2005/m3; median: 83.7 fg WHO-TEQ2005/m3) compared to those of dl-PCBs (3.9-36.8 WHO-TEQ2005/m3; median 9.9 WHO-TEQ2005/m3). A unique PCDD/F profile that was not previously reported was found. Further investigations should be conducted to establish whether the dioxin profile found in this study is specific for the desulfurization facility located in the study area or from oil flaring in the oil fields located upstream of the study area. The findings suggest that the oil field activities have a significant impact on the PCDD/F concentration in ambient air but a low or negligible influence on dl-PCBs' levels.

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.

Synthetic Phenolic Antioxidants and Their Metabolites in Indoor Dust from Homes and Microenvironments.

Synthetic phenolic antioxidants (SPAs), including 2,6-di-tert-butyl-4-hydroxytoluene (BHT), are extensively used in food, cosmetic and plastic industries. Nevertheless, limited information is available on human exposures, other than the dietary sources, to SPAs. In this study, occurrence of 9 SPAs and their metabolites/degradation products was determined in 339 indoor dust collected from 12 countries. BHT was found in 99.5% of indoor dust samples from homes and microenvironments at concentrations that ranged from < LOQ to 118 µg/g and 0.10 to 3460 µg/g, respectively. This is the first study to measure BHT metabolites in house dust (0.01-35.1 µg/g) and their concentrations accounted for 9.2-58% of the sum concentrations (∑SPAs). 3,5-di-tert-butyl-4-hydroxybenzaldehyde (BHT-CHO), 2,6-di-tert-butyl-4-(hydroxymethyl)phenol (BHT-OH), 2,6-di-tert-butyl-1,4-benzoquinone (BHT-Q) were the major derivatives of BHT found in dust samples. The concentrations of gallic acid esters (gallates) in dust from homes and microenvironments ranged from < LOQ to 18.2 and < LOQ to 684 µg/g, respectively. The concentrations and profiles of SPAs varied among countries and microenvironments. Significantly elevated concentrations of SPAs were found in dust from an e-waste workshop (1530 µg/g). The estimated daily intake (EDI) of BHT via house dust ingestion ranged from 0.40 to 222 ng/kg/d (95th percentile).

A comparative assessment of human exposure to tetrabromobisphenol A and eight bisphenols including bisphenol A via indoor dust ingestion in twelve countries.

Tetrabromobisphenol A (TBBPA) and eight bisphenol analogues (BPs) including bisphenol A (BPA) were determined in 388 indoor (including homes and microenvironments) dust samples collected from 12 countries (China, Colombia, Greece, India, Japan, Kuwait, Pakistan, Romania, Saudi Arabia, South Korea, U.S., and Vietnam). The concentrations of TBBPA and sum of eight bisphenols (Æ©BPs) in dust samples ranged from <1 to 3600 and from 13 to 110,000 ng/g, respectively. The highest TBBPA concentrations in house dust were found in samples from Japan (median: 140 ng/g), followed by South Korea (84 ng/g) and China (23 ng/g). The highest ∑BPs concentrations were found in Greece (median: 3900 ng/g), Japan (2600 ng/g) and the U.S. (2200 ng/g). Significant variations in BPA concentrations were found in dust samples collected from various microenvironments in offices and homes. Concentrations of TBBPA in house dust were significantly correlated with BPA and ∑BPs. Among the nine target chemicals analyzed, BPA was the predominant compound in dust from all countries. The proportion of TBBPA in sum concentrations of nine phenolic compounds analyzed in this study was the highest in dust samples from China (27%) and the lowest in Greece (0.41%). The median estimated daily intake (EDI) of ∑BPs through dust ingestion was the highest in Greece (1.6-17 ng/kg bw/day), Japan (1.3-16) and the U.S. (0.89-9.6) for various age groups. Nevertheless, in comparison with the reported BPA exposure doses through diet, dust ingestion accounted for less than 10% of the total exposure doses in China and the U.S. For TBBPA, the EDI for infants and toddlers ranged from 0.01 to 3.4 ng/kg bw/day, and dust ingestion is an important pathway for exposure accounting for 3.8-35% (median) of exposure doses in China.

A survey of cyclic and linear siloxanes in indoor dust and their implications for human exposures in twelve countries.

Siloxanes are used widely in a variety of consumer products, including cosmetics, personal care products, medical and electrical devices, cookware, and building materials. Nevertheless, little is known on the occurrence of siloxanes in indoor dust. In this survey, five cyclic (D3-D7) and 11 linear (L4-L14) siloxanes were determined in 310 indoor dust samples collected from 12 countries. Dust samples collected from Greece contained the highest concentrations of total cyclic siloxanes (TCSi), ranging from 118 to 25,100ng/g (median: 1380), and total linear siloxanes (TLSi), ranging from 129 to 4990ng/g (median: 772). The median total siloxane (TSi) concentrations in dust samples from 12 countries were in the following decreasing order: Greece (2970ng/g), Kuwait (2400), South Korea (1810), Japan (1500), the USA (1220), China (1070), Romania (538), Colombia (230), Vietnam (206), Saudi Arabia (132), India (116), and Pakistan (68.3). TLSi concentrations as high as 42,800ng/g (Kuwait) and TCSi concentrations as high as 25,000ng/g (Greece) were found in indoor dust samples. Among the 16 siloxanes determined, decamethylcyclopentasiloxane (D5) was found at the highest concentration in dust samples from all countries, except for Japan and South Korea, with a predominance of L11; Kuwait, with L10; and Pakistan and Romania, with L12. The composition profiles of 16 siloxanes in dust samples varied by country. TCSi accounted for a major proportion of TSi concentrations in dust collected from Colombia (90%), India (80%) and Saudi Arabia (70%), whereas TLSi predominated in samples collected from Japan (89%), Kuwait (85%), and South Korea (78%). Based on the measured median TSi concentrations in indoor dust, we estimated human exposure doses through indoor dust ingestion for various age groups. The exposure doses ranged from 0.27 to 11.9ng/kg-bw/d for toddlers and 0.06 to 2.48ng/kg-bw/d for adults.

Occurrence of perchlorate in indoor dust from the United States and eleven other countries: implications for human exposure.

Perchlorate is a widespread environmental contaminant and potent thyroid hormone disrupting compound. Despite this, very little is known with regard to the occurrence of this compound in indoor dust and the exposure of humans to perchlorate through dust ingestion. In this study, 366 indoor dust samples were collected from 12 countries, the USA, Colombia, Greece, Romania, Japan, Korea, Pakistan, Kuwait, Saudi Arabia, India, Vietnam, and China, during 2010-2014. Dust samples were extracted by 1% (v/v) methylamine in water. Analyte separation was achieved by an ion exchange (AS-21) column and analysis was performed by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The overall concentrations of perchlorate in dust were in the range of 0.02-104µg/g (geometric mean: 0.41µg/g). The indoor dust samples from China contained the highest concentrations (geometric mean: 5.38µg/g). No remarkable differences in perchlorate concentrations in dust were found among various microenvironments (i.e., car, home, office, and laboratory). The estimated median daily intake (EDI) of perchlorate for toddlers through dust ingestion in the USA, Colombia, Greece, Romania, Japan, Korea, Pakistan, Kuwait, Saudi Arabia, India, Vietnam, and China was 1.89, 0.37, 1.71, 0.74, 4.90, 7.20, 0.60, 0.80, 1.55, 0.70, 2.15, and 21.3ng/kgbodyweight (bw)/day, respectively. Although high concentrations of perchlorate were measured in some dust samples, the contribution of dust to total perchlorate intake was <5% of the total perchlorate intake in humans. This is the first multinational survey on the occurrence of perchlorate in indoor dust.

Screening for PCDD/Fs and dl-PCBs in local and imported food and feed products available across the State of Kuwait and assessment of dietary intake.

A total of 318 local and imported meat, milk, eggs, fish, and animal feed samples collected in Kuwait were analyzed by cell-based reporter gene assay (Dioxin-Responsive Chemical Activated LUciferase gene eXpression DR-CALUX) for PCDD/Fs and dl-PCBs. The bioanalytical equivalents (BEQs) obtained by DR-CALUX bioassay were compared with the official maximum limits according to the European Commission (EC) regulations. Suspected and randomly chosen negative samples were analyzed by gas chromatography-high resolution mass spectrometry (GC-HRMS). The results showed that among suspected samples, one sample was confirmed to be non-compliant. The positive sample was of imported origin. The correlation coefficient of 0.98 between DR-CALUX and GC-HRMS was found. Moreover, the average daily intakes of PCDD/Fs and dl-PCBs for the Kuwaiti population were estimated. Results obtained in this study were discussed and compared with other published data.

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.

Depositional history of polychlorinated biphenyls in a dated sediment core from the northwestern Arabian Gulf.

The vertical distribution of polychlorinated biphenyls (PCBs) was measured in a dated sediment core from the northwestern Arabian Gulf to reconstruct their depositional history. The downcore profile showed an increase in concentrations from depth to a subsurface maximum of approximately 1,500 pg g(-1) in approximately 1991, followed by an exponential decrease to the sediment-water interface. Current concentrations of ΣPCBs are similar to levels predating the episodic input of PCBs in sediments dated coincident with the 1991 Arabian Gulf war. The spike in ΣPCB concentrations during the war may be related to the destruction of PCB-laden transformers during the conflict. The 15-fold decrease in ΣPCB concentrations from the period of maximum flux to prewar levels suggests that the factors delivering PCBs to sediments at present are similar to those that that existed before the war-related inputs.

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.