The study was designed to assess the seasonal variations in the quality and lipid profile of mussel meat (Mytilus galloprovincialis) harvested along the Bulgarian coast of the Black Sea. The trial period lasted from June to October, and the sampling was carried out in the area of Varna Bay. Technological quality of the mussels was determined by measuring the water holding capacity (WHC) and cooking and roasting losses. Proximate composition, total aerobic plate count, and fatty acid analysis were carried out. Technological parameters and nutritional quality of the mussel meat were strongly affected by the season. During the summer, the mussels had higher mass, meat content, and meat yield (p < 0.001) compared to the early autumn, which corresponds to the lowest protein content during this season. Lipid profile showed seasonal variations in both individual and total fatty acid amounts (p < 0.001). Saturated fatty acids (SFA) had the highest content in summer, while monounsaturated fatty acids (MUFA) decreased gradually until the autumn. The content of polyunsaturated fatty acids (PUFA) reached its peak in October, contributing to the most favorable values of the nutritional indices of lipids in the early autumn.

Economically motivated or accidental species substitutions lead to economic and potential health damage to consumers with a loss of confidence in the fishery supply chain. In the present study, a three–year survey on 199 retail seafood products sold on the Bulgarian market was addressed to assess: (1) product authenticity by molecular identification; (2) trade name compliance to the list of official trade names accepted in the territory; (3) adherence of the list in force to the market supply. DNA barcoding on mitochondrial and nuclear genes was applied for the identification of whitefish (WF), crustaceans (C) and mollusks (cephalopods—MC; gastropods—MG; bivalves—MB) except for Mytilus sp. products for which the analysis was conducted with a previously validated RFLP PCR protocol. Identification at the species level was obtained for 94.5% of the products. Failures in species allocation were reconducted due to low resolution and reliability or the absence of reference sequences. The study highlighted an overall mislabeling rate of 11%. WF showed the highest mislabeling rate (14%), followed by MB (12.5%), MC (10%) and C (7.9%). This evidence emphasized the use of DNA–based methods as tools for seafood authentication. The presence of non–compliant trade names and the ineffectiveness of the list to describe the market species varieties attested to the need to improve seafood labeling and traceability at the national level.

Aim: This study aimed to evaluate the effect of dietary monosodium glutamate (MSG) on growth performance and blood biochemical parameters of rainbow trout (Oncorhynchus mykiss W.). Materials and Methods: A total of 200 trouts were allotted in five experimental groups (n=40) that for 60 days received feed supplemented with MSG at the following levels: 0% (K) or 0.5% (E) or 1% (F) or 3% (G) or 5% (H). Results: The average initial weight of trouts was 116.68±1.51 g (K), 116.58±1.33 g (E), 116.43±1.39 g (F), 117.40±1.47 g (G), and 115.95±1.88 g (H). At the end of the trial, control fish (K) had the lowest live weight (242.90±3.87 g) compared to Groups E (252.70±5.69 g), F (250.93±4.82 g), G (248.25±4.98 g), and H (247.95±4.74 g). Feed conversion ratio (FCR) of control group (K) was higher (1.11±0.02) versus FCR values established in Groups E (1.03±0.01), F (1.04±0.02), G (1.07±0.03), and H (1.06±0.02). Albumin, aspartate aminotransferase, gamma-glutamyl transpeptidase, alkaline phosphatase, phosphorus, magnesium, and triglyceride exhibited statistically significant differences versus controls. Conclusion: The results from the study showed that dietary supplementation of rainbow trouts with MSG increased live weight and reduced FCR. The optimum level of MSG recommended for addition to feed was 0.5%.