The features for assessing the authenticity of wines by region of origin are studied, based on the relationship between the mineral composition of the wine, the grapes, and the soil profile (0 to 160 cm) from the place of growth of Cabernet Sauvignon grapes. Soil, grape, and wine samples were taken from the territories of six vineyards in the Anapa district of Krasnodar Territory, Russia. Using the methods of ICP-OES, thermal, and X-ray phase analysis, the soils were differentiated into three groups, differing in mineralogical and mineral compositions. The soil samples of the first group contained up to 31% quartz, the second group up to 25% quartz and 19% mixed calcite, and the third group up to 32% calcite and 15% quartz. The formation of the elemental image of the grapes was studied, taking into account the total content and mobile forms of metals in the soil. The territorial proximity of the vineyards did not affect the extraction of elements from the soil into the grape berry, and the migration of metals for each territory was selective. According to the values of the biological absorption coefficient, the degree of transition of metals from the soil to a berry was estimated. For K, Ti, Zn, Rb, Cu, and Fe in all berries, the coefficient was higher than 1.00, which means that the berry extracts contained not only mobile-form, but also difficult-to-dissolve metal compounds. The migration of macro-components from the soil to the berry was low, and amounted to 6–7% for Ca, 0.8–3.0% for Na, and 25–70% for Mg of the concentration of their mobile forms. For all territories, the maximum correlation between metal concentrations in grapes and soil was observed for samples from a depth of 0–40 cm. The discriminant model based on concentrations of Rb, Al, K, Sr, Co, Na, Pb, Ca, and Ni showed the formation of clusters in the territories of vineyard cultivation. The developed model allow the problems of identifying wines by region to be solved with high accuracy, using their elemental image.

The aim of this work is to study the correlations of the elemental composition in the “soil–grape–wine” chain to determine the regional origin of Chardonnay grapes and wine. Soil samples (n = 40) from five vineyards in the Anapa region, Russia, taken from eight different depths, grapes from these vineyards (n = 75), and wines obtained from these grapes (n = 5) were analyzed using inductively coupled plasma atomic emission spectrometry and inductively coupled plasma mass spectrometry. The mineralogical composition of the soils was determined using thermal and X-ray phase analysis. The mineralogical composition of vineyard soils mainly consists of calcite, quartz, nontronite, vermiculite, and muscovite. According to spectrometric analysis, the distribution of both the total content and the mobile forms of elements in soil profiles turned out to be similar. The content of Na, Ca, and Sr increased with increasing sampling depth, while the content of Co, Cu, Fe, Ni, Mn, Pb, and Zn decreased. Regardless of the area of cultivation, the predominant elements in grapes are K, Ca, Na, and Mg. It is established that the elemental profiles of grapes and wine are correlated. At the same time, during the winemaking process, a decrease in the concentration of most elements (Al, Ba, Ca, Cu, K, Mg, Mn, Ni, Rb, Sr, Ti, and Zn) is observed. It has been shown that the vine is able to accumulate not only mobile but also less bioavailable forms of metals from the soil (Cu, Fe, K, Rb, Ti, and Zn), while the migration of Ca and Na remains low (<7%). Using discriminant analysis, a model of grape identification based on the concentrations of Al, Li, Mn, Na, Pb, and Rb was developed. This model demonstrated a high accuracy (100% for training and test datasets) in grape classification by region, confirming that the elemental “fingerprint” is a reliable marker of terroir.

To establish the relationship between the composition of wine and its regional origin, the most stable chemical parameters are selected because their variation is easiest to trace. Together with “classical” micro- and macroelements, rare earth elements (REEs) can be used for such purposes. However, the relationship between REE content in wine and its regional origin has not been systematically studied. This study examines the migration of REEs in the “soil-grape-wine” system to identify the relationship along the entire chain and establish the geographical origin of grapes and wine. The research was carried out on grapes and wines from the Chardonnay and Cabernet Sauvignon varieties, as well as soil samples selected from different vineyards. The concentrations of La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu in the studied samples were determined using ICP-MS. It was established that the studied soil samples are characterized by relatively low REE concentrations. Low transfer of REEs from soil to grapes was observed because the soils are rich in clay minerals that firmly retain these elements. Statistically significant differences in the REE content of grapes from different regions were detected (p < 0.05). Multidimensional analysis methods allowed us to group grape samples into clusters based on varietal and regional origin. Discriminant analysis showed the possibility of using the concentration of REEs as markers of the geographical origin of grapes. Of all the REEs, only La and Ce are reliably established in all wines. When determining the geographical origin of wine, the use of REE content is limited due to their very low concentrations in wine. In this regard, it has been proposed to use them in combination with macro- and microelements, which improves the classification performance of the model.

The paper shows the effect of organic fining agents on the formation of the elemental composition of young white wine of the Chardonnay variety. Substances of plant and animal origin and their mixtures were used as fining agents in the clarification of wines. The results were compared with clarification with activated calcium bentonite. In the untreated young wines from different areas of grape cultivation the concentrations of macroelements were 707–837 mg/L; minor elements—5.05–9.67 mg/L; microelements—0.033–0.058 mg/L; and rare earth elements (REEs)—0.001–1.350 µg/L. It was noted that organic agents have a smaller effect on the mineral composition of wine. The content of macroelements in wine decreased, regardless of the fining agent used (p < 0.01). After treatment with organic agents, the concentrations of Ti, Sr, Na and Ca increased, while the concentrations of Cu, Zr, Mo, Cs, Ba, W, Fe, Rb and K decreased. No increase in the REE content was observed. A moderate correlation (Pearson r = 0.69, 95% CI: 0.44–0.85, n = 30, p < 0.0001) was established between the applied concentration of Na in wine and its concentration in the fining agent. Despite changes, the elemental “image” of wine allows us to correctly determine the geographical origin of the drink. The most reliable markers were Li and Mn.