This paper elaborates soil, water, and lettuce contamination status with respect to selenium, sulphur, trace metals, and BTEX (benzene, toluene, ethylbenzene, and xylenes) in a coal-based area (Raša Bay, Adriatic Sea, Croatia). A local coal-fired power plant polluted soil with S, Se, Cd, and PAHs due to the combustion of domestic superhigh-organic-sulphur coal. The locality is dotted with waste from coal mining/separation, coal combustion, former metal factories, untreated municipal and coal mine effluents, along with various harbour activities, which contribute to environmental contamination. The methodology involved ICP-MS and GC-MS for the measurement of trace elements and BTEX, respectively, while soil sulphur was determined with Eschka’s mixture. The max values of the analysed trace elements in soil (mg/kg) are reported: Hg 1.14, Cd 3.29, V 624, Se 10.3, Pb 872, Cr 1860, Zn 6580, Cu 1850, and U 25.2. According to ecological indices, these values fall into the category of an extremely high level of soil pollution. Elevated total Se values in surface water are ascribed to leaching of seleniferous coal, ash, and coal-polluted soil. Levels of BTEX in water samples were very low (0–0.83 µg/L). The data provide basic information on the inorganic and organic contamination status of the Raša Bay area.

Milk containing aflatoxin M1 (ATM1) in quantities above 0.05 µg/kg is considered unsuitable for consumption. It is possible to use mycotoxin deactivators that bind aflatoxin M1 and allow the further use of milk. The study aimed to examine the impact of selected mycotoxin deactivators (beta-glucan from yeast and oats, and live and dead lactic acid bacteria) on the nutritional composition of milk after binding to aflatoxin M1 intentionally added to milk. The study used consumption milk with 2.8% milk fat intentionally contaminated with aflatoxin M1. Furthermore, 0.05% and 0.1% solutions of beta-glucan from yeast and beta-glucan from oats were added to the contaminated milk, as well as live and dead lactic acid. Concentrations of Na, K, Mg, and Ca were monitored at the zero hour of binding of mycotoxin deactivators and ATM1, after 2 h of binding, and after 4 and 24 h of binding. The largest deviations were found in Na, K, and Mg, while the minimum changes were observed in Ca. Live lactic acid bacteria were found to have the least impact on micronutrients, except in Na (difference = 40, p = 0.029, GES = 0.083), where the 0.1% solution from oats had the least impact on micronutrient content. The results of this study suggest that it is best to use live lactic acid bacteria where the different duration of action regarding nutrients, with the possible exception of Na, is not relevant, which indicates that, when using this mycotoxin deactivator, milk contaminated with ATM1 can be further used.

The aim of this study was to determine the quantity of particular toxic metals (Pb, Cd, As, Hg) and micronutrients (Cr, Fe, Co, Ni, Cu, Zn, Se) in the recommended daily dose of 51 food supplements based on beehive products. Samples taken from the Croatian market were submitted for the identification/quantification of studied metals and micronutrients. It was carried out by means of inductively coupled plasma mass spectrometry (ICP-MS). Eleven samples (21.57%) showed an increased concentration of total arsenic, three samples (5.88%) contained an increased concentration of total iron, and eight samples (15.68%) had an increased concentration of total nickel. Three samples (5.88%) contained an increased concentration of zinc, while one sample (1.96%) contained an increased concentration of selenium. Increased levels of certain toxic metals and micronutrients do not pose a danger to human health because the amount identified was less than what can cause toxic effects in humans. All other analysed metals and micronutrients fell within the defined literature values. Despite certain increases in particular parameters, all samples met the established toxicity criteria. This study evidenced their safety if consumed in the recommended daily dose.

Human activities inevitably affect natural ecosystems, the impact of which most often refers to negative factors resulting in the accumulation of toxic elements in environmental components. This study quantified the presence of 12 toxic elements (Cd, Co, Cr, Cu, Hg, Fe, Mn, Ni, Pb, Zn, As, and Se) in water, soil, and six melliferous plant species across the Republic of Croatia. Sampling sites were classified into four groups according to the dominant anthropogenic impact: agricultural areas, urban and traffic-affected zones, industrial vicinities, and forested hill regions. The results demonstrate the transfer of toxic elements from abiotic matrices into plants, indicating their potential as bioaccumulators. Soil contamination with toxic metals was identified as a relevant ecological risk factor, while contamination of melliferous plants highlights potential implications for human health through the production of honeybee-derived products. Element concentrations in water and soil were determined using three atomic absorption spectrometry techniques (FAAS, GFAAS, and CVAAS), whereas concentrations in floral samples of melliferous plants were measured using inductively coupled plasma mass spectrometry (ICP MS). The obtained results were interpreted in relation to natural background levels and the current national legislation. Anthropogenic impacts were further evaluated using environmental quality indices and bioaccumulation factors, revealing site-specific contamination patterns of both natural and anthropogenic origin.