The detailed mineralogical and microgeochemical characteristics of polymetallic nodules collected from the Interoceanmetal Joint Organization (IOM, Szczecin, Poland) claim area, Eastern Clarion-Clipperton Fracture Zone (CCFZ, Eastern Pacific) were described in this study. The obtained data were applied for the delimitation of nodule growth generations and estimation of the growth ratios (back-stripping using the Co-chronometer method). The applied methods included bulk X-ray powder diffraction (XRD) and electron probe microanalysis (EPMA), providing information about Mn-Fe minerals and clays composing nodules, as well as the geochemical zonation of the growth generations. The analyzed nodules were mostly diagenetic (Mn/Fe > 5), with less influence on the hydrogenous processes, dominated by the presence of 10-Å phyllomanganates represented by todorokite/buserite, additionally mixed with birnessite and vernadite. The specific lithotype (intranodulith), being an integral part of polymetallic nodules, developed as a result of the secondary diagenetic processes of lithification and the cementation of Fe-rich clays (potentially nontronite and Fe-rich smectite), barite, zeolites (Na-phillipsite), bioapatite, biogenic remnants, and detrital material, occurs in holes, microcaverns, and open fractures in between ore colloforms. The contents of ∑(Ni, Cu, and Co) varied from 1.54 to 3.06 wt %. Several remnants of siliceous microorganisms (radiolarians and diatoms) were found to form pseudomorphs. The applied Co-chronometer method indicated that the nodules’ age is mainly Middle Pliocene to Middle Pleistocene, and the growth rates are typical of diagenetic and mixed hydrogenetic–diagenetic (HD) processes. Additionally, few nodules showed suboxic conditions of nucleation. Growth processes in the eastern part of the CCFZ deposit might have been induced with the Plio-Pleistocene changes in the paleooceanographic conditions related to the deglaciation of the Northern Hemisphere.

Organotin compounds (OTCs) are among the most hazardous substances found in the marine environment and can be determined by either the ISO 23161 method based on extraction with non-polar organic solvents and gas chromatography analysis or by the recently developed QuEChERS method coupled to liquid chromatography-mass spectrometry (LC-MS/MS). To date, the QuEChERS LC/MS and ISO 23161 methods have not been compared in terms of their fit-for-purpose and reliability in the determination of OTCs in bottom sediments. In the case of ISO 23161, due to a large number of interferences gas chromatography-mass spectrometry was not suitable for the determination of OTCs contrary to more selective determination by gas chromatography with an atomic emission detector. Moreover, it has been found that the derivatization of OTCs to volatile compounds, which required prior gas chromatography determination, was strongly affected by the sediments’ matrices. As a result, a large amount of reagent was needed for the complete derivatization of the compounds. Contrary to ISO 23161, the QuEChERS LC-MS/MS method did not require the derivatization of OTC and is less prone to interferences. Highly volatile and toxic solvents were not used in the QuEChERS LC-MS/MS method. This makes the method more environmentally friendly according to the principles of green analytical chemistry. QuEChERS LC-MS/MS is suitable for fast and reliable environmental monitoring of OTCs in bottom sediments from the Odra River estuary. However, determination of di- and monobutyltin by the QuEChERS LC-MS/MS method was not possible due to the constraints of the chromatographic system. Hence, further development of this method is needed for monitoring di- and monobutyltin in bottom sediments.

The results from previous environmental studies on the physicochemical properties of bottom sediments from the Odra River estuary (SW Baltic Sea) and their contamination by pharmaceutically active compounds (PhACs) were compiled and analyzed by the use of various statistical methods (Principal Component Analysis, ANOVA/Kruskal–Wallis, Spearman correlation analysis, Partial Least Squares Discriminant Analysis, and Cluster Analysis). These studies included data on 130 PhACs determined in sediment samples collected from 70 sites across the Odra River estuary as well as the site distance to wastewater treatment plant discharge, PhACs’ physicochemical properties (Kd, Kow, pKa, solubility, metabolism), and sales data. Additionally, total organic carbon, total nitrogen, total phosphorus, acid volatile sulfides, clay mineral content, and trace elements such as As, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sn, and Zn were analyzed. Clay mineral content and TP were identified as the key physicochemical factors influencing the spatial distribution of PhACs in bottom sediments, exerting a greater impact than the distance of sampling sites from WWTP discharge points. The distribution of PhACs in the estuary was also influenced by the Kd and solubility of the compounds. More soluble pharmaceuticals with low adsorption affinity to sediments were detected more frequently and transported to distant locations, whereas less soluble compounds with high adsorption affinity settled down in bottom sediments near contamination sources. Neither the proportion of a drug excreted unchanged, nor its prescription frequency and sales volume, influenced the spatial distribution of PhACs. In general, Kd may be a useful parameter in the planning of environmental monitoring and tracing migration of PhACs in aquatic environments.