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• A passive sampler was developed to measure inorganic and organic pollutants synchronously. • Vertical resolution of centimeters for pollutants could be obtained by the sampler. • The sediment role of source or sink for pollutant was identified by the passive sampler. In situ measurement of multiple pollutants coexisting in sediment porewater is an essential step in comprehensively assessing the bioavailability and risk of pollutants, but to date, this needs to be better developed. In this study, a passive sampler, consisting of an "I-shaped" supporting frame and inorganic/organic sampling units, incorporating equilibrium dialysis theory and kinetic/equilibrium sorption principle, was developed for the synchronous measurement of inorganic (e.g., phosphorus and metal(loid)s) and organic pollutants (e.g., parent and substituted PAHs). The equilibrium time and sampling rates were explored in laboratory tests to support in situ application. Profiles of pollutants in porewater within a vertical resolution of centimeters, i.e., 1 cm and 2 cm for inorganic and organic pollutants, respectively, were obtained by field deployment of the sampler for further estimation of diffusive fluxes across the sediment-water interface. The results suggested that the role of sediments for a specific pollutant may change (e.g., from "sink" to "source") during the sampling time. This study demonstrated the feasibility of synchronous measurement of inorganic and organic pollutants in sediment porewater by the passive sampler. In addition, it provided new insight for further investigation into the combined pollution effects of various pollutants in sediments. [Display omitted] [ABSTRACT FROM AUTHOR]

Mercury (Hg) could be microbially methylated to the bioaccumulative neurotoxin methylmercury (MeHg), raising health concerns. Understanding the methylation of various Hg species is thus critical in predicting the MeHg risk. Among the known Hg species, mercury sulfide (HgS) is the largest Hg reservoir in the lithosphere and has long been considered to be highly inert. However, with advances in the analytical methods of nanoparticles, HgS nanoparticles (HgS NPs) have recently been detected in various environmental matrices or organisms. Furthermore, pioneering laboratory studies have reported the high bioavailability of HgS NPs. The formation, presence, and transformation (e.g., methylation) of HgS NPs are intricately related to several environmental factors, especially dissolved organic matter (DOM). The complexity of the behavior of HgS NPs and the heterogeneity of DOM prevent us from comprehensively understanding and predicting the risk of HgS NPs. To reveal the role of HgS NPs in Hg biogeochemical cycling, research needs should focus on the following aspects: the formation pathways, the presence, and the environmental behaviors of HgS NPs impacted by the dominant influential factor of DOM. We thus summarized the latest progress in these aspects and proposed future research priorities, e.g., developing the detection techniques of HgS NPs and probing HgS NPs in various matrices, further exploring the interactions between DOM and HgS NPs. Besides, as most of the previous studies were conducted in laboratories, our current knowledge should be further refreshed through field observations, which would help to gain better insights into predicting the Hg risks in natural environment. [Display omitted] [ABSTRACT FROM AUTHOR]