A total of 208 polycyclic aromatic compounds and their substituted homologues were investigated on eight stations along Croatia-Italy transect in the Middle Adriatic. PAC concentrations were higher in the coastal area than in the open sea area. The highest PAC concentrations were measured in the vicinity of the industrial harbor of Split while the lowest concentrations were observed on stations located in the open sea area. Polycyclic aromatic hydrocarbons were dominant group of compounds on each investigated station with contributions in total PAC concentration of more than 85%. S-PAH concentrations were higher than O-PAH concentration in each sample and tend to decrease as the distance from the coast increased. Contributions of O-PAH in total PAC concentrations were higher in the open sea sediments while S-PAH contributions were higher in the coastal sediment, indicating a different origin of O-PAH. Grain size analysis of the investigated sediments shows the dominance of fine fraction in sediments in the coastal area whereas sandy particles were a dominant fraction in the open sea sediments. TOC concentrations were higher in the open sea area where lower PAH concentrations were observed, indicating a different origin of PAC and TOC. PAH origin was evaluated by application of diagnostic ratios. Pyrogenic origin was determined only on one station whereas dominance of petrogenic PAHs was observed on the most of the stations in the open sea area. Marine traffic was suspected to be the main source of pollution in the open sea area.

The Krka River estuary is a karstic, permanently stratified estuary due to the strong freshwater inflow. It is a special environment in which to study the phytoplankton community, especially because this area is an important aquaculture site. Among other potentially toxic phytoplankton species, the diatom genus Pseudo-nitzschia occurs frequently and is a potential source of domoic acid (DA), causing shellfish toxicity and human intoxication. The main objective was to examine the dynamics of the phytoplankton community and, in particular, the genus Pseudo-nitzschia in the upper part of the Krka estuary, through monthly sampling over two years. The phytoplankton community was analysed using light microscopy and scanning electron microscopy to determine the diversity of Pseudo-nitzschia species and characterise the environmental parameters associated with a high abundance of Pseudo-nitzschia species. Seven Pseudo-nitzschia species were identified in the investigation, with higher frequencies and abundances in the less variable layer, at a 7 m depth. Blooms of Pseudo-nitzschia were noted in the late summer/early autumn, dominated by P. delicatissima/arenysensis. Winter assemblages were characterised by P. pseudodelicatissima/cuspidata, P. calliantha, and P. subfraudulenta, and were associated with domoic acid occurrence in shellfish.

An improved methodology was developed for V redox speciation in estuarine waters using a hyphenated technique consisting of ion chromatograph (IC) with an anion exchange column and a high-resolution inductively coupled plasma mass spectrometer (HR ICP-MS). This approach enables the direct determination of V(V), whereas reduced species (mainly V(IV)) are calculated by subtracting V(V) concentrations from the measured total V concentration. Based on the “on-column” V(V) chelation mechanism by EDTA, with the eluent composed of 40 mmol L⁻¹ ammonium bicarbonate, 40 mmol L⁻¹ ammonium sulphate, 8 mmol L⁻¹ ethylenediaminetetraacetic acid and 3% acetonitrile, the method was successfully used for analyses of V redox speciation in samples taken in the vertical salinity gradient of the highly stratified Krka River estuary. Due to the matrix effects causing different sensitivities, a standard addition method was used for V(V) quantification purposes. The limit of detection (LOD) was also found to be matrix related: 101.68 ng L⁻¹ in the seawater and 30.56 µg L⁻¹ in the freshwater. Performed stability tests showed that V redox speciation is preserved at least 7 days in un-treated samples, possibly due to the stabilization of V-reduced species with natural organic matter (NOM). The dominant V form in the analysed samples was V(V) with the reduced V(IV) accounting for up to 26% of the total dissolved pool. The concentration of V(IV) was found to correlate negatively with the oxygen concentration. Significant removal of dissolved V was detected in oxygen depleted zones possibly related to the particle scavenging.

Concentrations of polycyclic aromatic hydrocarbons (PAH) were studied in 36 sediment samples collected from 29 sites in the central Adriatic Sea. The total concentration of PAH showed high variability, ranging from 42.85 µg kg⁻¹ in open sea sediments to 28,662 µg kg⁻¹ in the sediments of Šibenik Bay. Unsubstituted, parent PAH were dominant PAH compounds in the entire area of Šibenik Bay and most of the stations in the coastal area. In Kaštela Bay, methyl PAH concentrations were higher than the concentrations of unsubstituted PAH, whereas in the sediments along the mid-Adriatic transect, similar concentrations of both PAH fractions were determined. PAH sources were investigated by applying the Positive Matrix Factorization software developed by the U.S. Environmental Protection Agency (USEPA). The results indicate the presence of four sources, two of which can be considered petrogenic and two pyrogenic. The contribution of the sources to the total concentration PAH at each station indicates the dominance of pyrogenic sources in Šibenik Bay and at most stations in the coastal area. In the sediments along the mid-Adriatic transversal, as well as in Kaštela Bay, PAHs originate mainly from petrogenic sources. The obtained results show that PMF can be a suitable tool for control of PAH pollution and thus, for the management of various activities in the Adriatic region. Seasonal differences between the contributions of sources in the Kaštela and Šibenik bays indicate that the contribution of traffic to the total concentration of PAH was higher during the tourist season. The carcinogenic risk of PAH determined by toxicity equivalent (TEQ) calculations showed an increased carcinogenic risk in the whole area of Šibenik Bay, regardless of the number of PAH compounds considered for the calculations. A low PAH-related carcinogenic risk was found for the rest of the study area.