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Important biogeochemical processes occur in sediments at fine scales. Sampling techniques capable of yielding information with high resolution are therefore needed to investigate chemical distributions and fluxes and to elucidate key processes affecting chemical fates. In this study, a high-resolution diffusive gradients in thin-films (DGT) technique was systematically developed and tested in a controlled sediment system to measure organic contaminants, antibiotics, for the first time. The DGT probe was used to resolve compound distributions at the mm scale. It also reflected the fluxes from the sediment pore-water and remobilization from the solid phase, providing more dynamic information. Through the fine scale detection, a reduction of re-supply was observed over time, which was concentration and location dependent. Compared to the Rhizon sampling method, antibiotic concentrations obtained by DGT probes were less than the pore-water concentrations, as DGT measures the labile fraction of the compounds. The DGT probe was also tested on an intact sediment core sampled from a lake in China and used to measure the distribution of labile antibiotics with depth in the core at the mm scale. The abuse of antibiotics and widespread of their residues influences the ecosystem, induces the generation of super-bacteria, and finally poses threat to human health. Sediments adsorbs pollutants from the aquatic environment, while may also release them back to the environment. We systematically developed DGT probe approach for measuring antibiotics in sediment in situ in high resolving power, it provides information at fine scale to help us investigate biogeochemical processes take place in sediment and sediment-water interface. [Display omitted] • Developed a new in situ high resolution sampling probe for studying antibiotics. • Resolving power reached the mm scale, better than conventional methods. • Vertical distribution of antibiotics in sediments and their transport were determined. • Antibiotics were detected in an intact sediment core using DGT probe. [ABSTRACT FROM AUTHOR]

A new method for the determination of 26 legacy and emerging per- and polyfluoroalkyl substances (PFASs) in marine sediment pore water was developed using online solid phase extraction coupled with liquid chromatography-tandem mass spectrometry. The proposed method requires only about 1 mL of pore water samples. Satisfactory recoveries of most target PFASs (83.55–125.30 %) were achieved, with good precision (RSD of 1.09–16.53 %), linearity (R 2 ≥ 0.990), and sensitivity (MDLs: 0.05 ng/L–5.00 ng/L for most PFASs). Subsequently, the method was applied to determine PFASs in the sediment pore water of five mariculture bays in the Bohai and Yellow Seas of China for the first time. Fifteen PFASs were detected with total concentrations ranging from 150.23 ng/L to 1838.48 ng/L (mean = 636.80 ng/L). The ∑PFASs and PFOA concentrations in sediment pore water were remarkably higher than those in surface seawater (tens of ng/L), indicating that the potential toxic effect of PFASs on benthic organisms may be underestimated. PFPeA was mainly distributed in pore water, and the partition of PFHpA (50.99 %) and PFOA (49.01 %) was almost equal in the solid and liquid phases. The proportions of all other PFASs partitioned in marine sediments were significantly higher than those in pore water. [Display omitted] • A convenient method for the detection of PFASs in marine sediment pore water was developed. • Only about 1 mL of actual sediment pore water is needed to determine various PFASs. • High levels of PFASs were detected in pore water from five mariculture bays of China. • Different PFASs exhibit varying partitioning behaviors at the sediment–pore water interface. • Great attention should be paid to PFASs in the sediment pore water of mariculture areas. [ABSTRACT FROM AUTHOR]

Understanding various biogeochemical processes, especially in eutrophic sediments, necessitates fine-scale phosphorus (P) measurements in pore waters. To the best of our knowledge, the fine-scale distributions of P across the sediment profiles of Lake Nansi have rarely been investigated. Herein we evaluated the dynamic distributions of labile P and Fe across the sediment-water interface (SWI) of Lake Nansi at two-dimensional (2D) and sub-millimeter resolution, using well-established colorimetric diffusive gradients in thin films (DGT) methodology. The concentrations of labile P in all investigated sediment profiles exhibited strong spatial variations, ranging from 0 to 1.50 mg/L with a considerable number of hotspots. Lake Nanyang (0.55 ± 0.21 mg/L) had the highest mean concentration of labile P, followed by Lake Dushan (0.38 ± 0.19 mg/L), Lake Weishan (0.28 ± 0.21 mg/L), and Lake Zhaoyang (0.18 ± 0.09 mg/L). The highest concentrations of labile P were always detected in Lake Dushan, which had been subjected to excessive exogenous P pollution. The co-distributions of labile P and Fe in the majority of the sediment of Lake Nansi confirmed highly positive correlations (P < 0.01), suggesting that the mobility of labile P throughout the SWI was likely governed by iron redox processes. The apparent diffusion fluxes of P across the SWI ranged from −7.7 to 33.6 μg/m2·d, with a mean value of 5.26 ± 7.80 μg/m2·d. Positive apparent fluxes for labile P were recorded in most sediment cores, demonstrating the strong upward mobility of P from the sediment to the overlying water. Our results provided accurate and extensive information regarding the micro-distribution and dynamic exchange of labile P across the SWI. This allows for a better understanding of eutrophication processes and the implementation of P management strategies in Lake Nansi. [Display omitted] • The spatial variation and mobility of P in Lake Nansi were characterized using DGT. • 2D, heterogeneously micro-distribution of P in the sediment profile was observed. • Labile P had a northward and downward spatial gradient, related to human activity. • The mobility of P across the SWI was likely governed by iron redox processes. • Fine-scale measurement improves the accuracy P-cycle depiction for eutrophic lake. [ABSTRACT FROM AUTHOR]