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Surface sediments (n = 124) were gathered to evaluate spatial pattern and source apportionment of ∑ 24 n-alkanes in the Persian Gulf. Moran's I indices revealed that ∑ 24 n-alkanes were randomly distributed in sampling space in general. One noticeable exception was a significant spatial high-high cluster (Z-score = 8.6). Profile of n-alkanes observed for this cluster maximized at n-C 20 , n-C 18 , n-C 16 , and n-C 22 . Detection of very low carbon preference indices and strong even carbon-numbered predominance suggested that bacterial inputs were the process making this cluster. Based on diagnostic ratios and GIS techniques, in situ production of organic materials was widespread in the studied space. Allochthonous and petroleum-based inputs were not traceable for 73.8% and 24.7% of the area, respectively. Petrogenic source apportionment map proposed that petroleum-originated contaminants were probably limited to 6.32 km 2 of the sampling matrix. The biogenic inputs (autochthonous and allochthonous inputs) and not the petroleum contaminants were the main source of n-alkanes deposited.

Surface sediments (n = 35) and a core sample around Pars Special Economic Energy Zone were analyzed to address spatiotemporal variations of heavy metals. Enrichment factors classified the elements as: (1) poorly enriched, geogenic elements (Co, Cr, Fe, Li, Mn, Mo, Ni, Ti, and V), (2) minimal enriched elements (Zn and Mg), (3) moderately enriched elements (Ag, Cd, Pb, Se, and Sr), and (4) significantly enriched element (As and Hg). The core profile showed that As, Hg, Ag, and Cd had considerable anthropogenic inventories. Arsenic levels were continuously increasing toward the top of the core and sedimentary cycling was not an effective factor on its enrichment. Pollution load index classified the area as a severely affected region and Risk Index values suggested that 57% of the sediments had a moderate potential risks. The mapping techniques proposed a polluted and hazardous patch at the entrance and center part of the Nayband Bay., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Surface sediments (n=17) were collected from 6 sites located in the coasts of the Bushehr Peninsula. ∑ 16 PAH concentrations were in the range of 285.9-1288ngg -1 dw and the sediments were moderately polluted. Py, Ph, B(a)A and Flu showed >70% of the detected values in order of the mentioned rank. 4-ring PAHs were the dominant compounds and the molecular ratios presented the dominant pyrolytic source. The toxicity of PAHs for sediment dwelling life was averagely equivalent to occurrence of 0.08ngg -1 of Dioxin in dw of the examined sediments. The evaluated narcotic potential (confidence level of 99%) was 0.027-3.04 and upper part of the Bushehr Peninsula, where the human population is more concentrated, showed more narcotic potential. ∑n-alkane concentrations (n-C 15 -n-C 32 ) were in the range of 3.10-35.6μgg -1 dw. The dominant distribution of even carbon number n-alkanes was traced back to a possibly autochthonous source., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

In the present study, antifouling paint booster biocides, Irgarol 1051 and diuron were measured in ports and marinas of Bushehr, Iran. Results showed that in seawater samples taken from ports and marinas, Irgarol was found at the range of less than LOD to 63.4ngL(-1) and diuron was found to be at the range of less than LOD to 29.1ngL(-1) (in Jalali marina). 3,4-dichloroaniline (3,4-DCA), as a degradation product of diuron, was also analyzed and its maximum concentration was 390ngL(-1). Results for analysis of Irgarol 1051 in sediments showed a maximum concentration of 35.4ngg(-1) dry weight in Bandargah marina. A comparison between the results of this study and those of other published works showed that Irgarol and diuron pollutions in ports and marinas of Bushehr located in the Persian Gulf were less than the average of reports from other parts of the world., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Dissolved carbon dioxide flotation after emulsification microextraction (DCF-EME) technique coupled with gas chromatography-electron capture detection (GC-ECD) was introduced for preconcentration and determination of six organochlorine pesticides (OCPs) in seawater samples. DCF-EME method is based on the rapid and simple phase separation of low density organic solvent from the aqueous phase via introducing of a saturated NaHCO3 solution (9.6% w/v) into the acidified sample solution (0.1M of HCl) containing analytes. Thanks to the in situ generation of carbon dioxide (CO2) bobbles intensified by ultrasound radiation, the dispersed extraction solvent was collected to the surface of the aqueous sample and then was narrowed to the capillary part of a special home-made extraction cell for facile retrieving. Under the optimal conditions, the limits of detection were at the range of 2.6-9.2 ng L(-1) and preconcentration factors were varied between 271 and 307 for different OCPs. The applicability of the developed method was evaluated by the extraction and determination of the target analytes from Caspian seawater samples., (Copyright © 2015 Elsevier B.V. All rights reserved.)

In the present work, microfunnel-supported liquid-phase microextraction method (MF-LPME) based on applying low density organic solvent was developed for the determination of antifoulings (Irgarol 1051, diuron and 3,4-dichloroaniline) from seawater samples. In this method, home-designed MF device was used for facile loading and retrieving of organic solvent during the extraction procedure. The extraction was carried out with introduction of 400 μL of toluene via syringe into the MF device placed on the surface of sample solution (300 mL) containing analytes. After the extraction, extractant layer was narrowed into the capillary part of MF by pushing the device inside the sample and withdrawn by using a syringe to evaporate by nitrogen purging. The residual redissolved into 50 μL methanol, diluted to 100 μL with deionized water and injected into the high performance liquid chromatography with UV detection (HPLC-UV). Several factors influencing the extraction such as the type and volume of extraction solvent, sample pH, extraction time and ionic strength were investigated and optimized. Under the optimized conditions, the limits of detection in seawater were 1.4, 4.8 and 1.0 ng L(-1) for 3,4-dichloroaniline (DCA), diuron and Irgarol 1051, respectively. Enrichment factors were obtained 333, 150 and 373 for DCA, diuron and Irgarol 1051, respectively. The precision of the technique was evaluated in terms of repeatability which was less than 12.0% (n=5). The applicability of the proposed method was evaluated by the extraction and determination of antifoulings from seawater samples collected from harbors of Bushehr located in northern Persian Gulf coast., (Copyright © 2014 Elsevier B.V. All rights reserved.)