The present work aimed at the development of a simple and accurate direct immersion-solidphase microextraction-gas-chromatography-mass spectrometry (DI-SPME-GC-MS) method for simultaneous determination of PAHs, PCBs, and pesticide residues in edible seaweeds. As the target contaminants possess a wide range of physical-chemical properties, multivariate experimental design was used for method optimization. In particular, two different methods were optimized and validated: one that allows for simultaneous determination of all targets, and an ad hoc method for determination of hydrophobic analytes, a class that often poses a challenge for extraction from food matrices. Optimum conditions suitable for simultaneous quantitation of all targeted compounds, namely buffer at pH = 7.0, 20% acetone (v/v), 10% NaCl (w/w), 0.02% NaN3, 60 min DI extraction at 55 °C, and 20 min desorption at 270 °C, afforded limits of quantitation (LOQs) in the range of 1-30 μg kg-1, a wide linear range of 5-2000 μg kg-1, the attainment of satisfactory determination coefficients (R2˃0.99) with no significant lack of fit (p > 0.05) at the 5% level, and satisfactory accuracy and precision values. By modifying the extraction conditions to favor extraction of the most hydrophobic analytes (e.g. higher amount of organic modifier and pH, and lower salt content) lower LOQs were obtained for these compounds ranging from 0.2 to 13.3 μg kg-1. The established methods were then used for screening of commercial, edible dry seaweeds, with PCBs (≤16.0 ng g-1) and PAHs (≤15.5 ng g-1) detected in some samples. This method overcomes most challenges commonly encountered in dry sample analysis applications, and represents the first report of a DI-SPME method employing the matrix-compatible fiber for simultaneous multiclass and multiresidue analysis of seaweeds.

With the prohibition of conventional organochlorine pesticides (OCPs), the extensive use and continuous release of current-use pesticides (CUPs), such as organic amine pesticides (OAPs) and organophosphate pesticides (OPPs), in agriculture and mariculture activities have raised global attention. In this study, the occurrence and distribution of 36 pesticides from above 3 categories were investigated in seawater and sediment in Beibu Gulf, a typical subtropical agricultural and maricultrual zone. Results showed that pesticides were widely present in this region with the total concentration ranging from 0.36 to 21.07 ng/L in seawater and from 0.02 to 9.73 ng/g dw in sediment. OAPs and OPPs were the most abundant categories contributing 74% and 66% to the total pesticides burden in seawater and sediment, respectively, revealing the current-use pesticides as substitutes of legacy organochlorine pesticides (OCPs) were mainly used in surrounding areas. For both seawater and surface sediment, the spatial distribution of pesticides concentrations showed generally seaward decreasing trends, suggesting that anthropogenic activities at coastal areas have an important impact on pesticides pollution. Source identification indicated OCPs in some seawater samples might be from mixture of antifouling paint and dicofol usage, while history residues are main sources of OCPs in sediment. OAPs, especially for cyflufenamid and kresoxim-methyl, mainly come from agricultral and maricultural sewage input, and OPPs were speculated from currency transportation from surrounding areas. Ecological risk assessment showed that OPPs posed moderate to even high risks in most seawater sites. It appears that crustaceans are the most sensitive trophic species to OPPs among aquatic organisms, followed by fish. According to the results of health risks proposed by the major aquatic products in Beibu Gulf (fish and shrimp), the selected pesticides pose no health risk to humans. Nevertheless, OCPs made the highest contribution to the total HQ values. Comprehensively considering the evaluation results of both ecological and health risks, more attention should be given on OPPs and OCPs pollution in the Beibu Gulf.