Dissolved organic carbon (DOC) is an essential component of the biogeochemical marine system, effecting biological and chemical reactions that take place in the sea. DOC represents a dynamic component of the global carbon cycle. This paper reports 25years of measurements of DOC content and distribution at seven stations along the transect Po River delta - Rovinj in the northern Adriatic (NA). The results show strong temporal and spatial variability: (1) The highest average DOC concentrations were observed in 1998 and 2002 (143μmol/L and 137μmol/L, respectively); (2) The minimum average DOC was recorded in 2006 (88μmol/L) and (3) The short-term DOC accumulation (up to 203, average 102μmol/L) for the years 2009 to 2012, was observed during the summer and autumn months followed by unusually low DOC concentrations during the winter and spring. The DOC results from the more recent monitoring at the same stations indicate primarily oligotrophic characteristics of the NA seawater (88μmol/L). The results of DOC variability and distribution in the NA appears to be strongly influenced by complex circulation patterns. This paper provides a "link" between the Ionian circulation and the NA ecosystem as a part of the recently identified Adriatic-Ionian Bimodal Oscillating System (BiOS). A good agreement between the BiOS oscillation and other variables related to the DOC concentration, like the NA A and B winter types, the Po River discharge, salinity, chlorophyll a, occurrence of hypoxic-anoxic conditions, eutrophication and oligotrophication, suggests that DOC might be a good tool and indicator of global change.

The characterization of organic matter (OM) and trace elements (TEs) was conducted in bulk precipitation samples collected in an urban area of Croatia (Zagreb center), from January 2009 to October 2011 (N = 31). Characterization of OM was performed by measurement of dissolved (DOC) and particulate forms of organic carbon (POC), as well as surface-active substances, copper complexing capacity and reduced sulfur species which were determined electrochemically. Concentrations of TEs (Al, Fe, Zn, Cr, Ba, Mn, Cu, Sr, Ti, Pb, V, Ni, Rb, Sb, As, Sn, Se, Co, Cd, Mo) were analyzed by HR ICP-MS. The most important outcome of this study is confirmed relatively low concentrations of DOC (0.69–4.86 mgC L⁻¹) and TEs. Daily fluxes of Zn, Pb, Ni, As, and Cd were two to three times lower than that of those reported for an urban industrial site in Europe. Additionally, this study shows that the value and reactivity of rainwater DOC has not considerably changed if compared with the results from the 1998–1999 study (0.78–4.39 mgC L⁻¹). High traffic density and thermal power plants are assumed to be the main local sources of pollutants in Zagreb. Using Al as a reference element, it was found that Cd, Sb, and Cu were associated with anthropogenic sources. The solubility of Sr, Zn, Cd, Ni, Cr, As, and Rb was higher than 70%. Another critical characteristic of precipitation composition is episodic variation in POC concentration because of Saharan dust transport. Obtained data can be valuable for environmental quality assessment, as well as for insight into atmospheric deposition processes.

Elemental sulfur (S) persists in natural aquatic environment in a variety of forms with different size distributions from dissolved to particulate. Determination of S speciation mainly consists of the application of chromatographic and electrochemical techniques while its size determination is limited only to the application of microscopic and light scattering techniques. S biological and geochemical importance together with recent increases of S industrial applications requires the development of different analytical tools for S sizing and quantification. In recent years the use of electrochemical measurements as a direct, fast, and inexpensive technique for the different nanoparticles (NPs) characterization (Ag, Au, Pt) is increasing. In this work, electrochemical i.e. chronoamperometric measurements at the Hg electrode are performed for determination of the size distribution of the S NPs. S NPs were synthesized in aqueous medium by sodium polysulphide acidic hydrolysis. Chronoamperometric measurements reveal the polydisperse nature of the formed suspension of S NPs. The electrochemical results were compared with dynamic light scattering measurements parallel run in the same S NPs suspensions. The two methods show fairly good agreement, both suggesting a log-normal size distribution of the S NPs sizes characterized by similar parameters. The preliminary results highlight the amperometric measurements as a promising tool for the size determination of the S NPs in the water environment.