D. Weber et al., CORRELATIONS OF CARBON-ISOTOPE RATIOS OF WINE INGREDIENTS FOR THE IMPROVED DETECTION OF ADULTERATIONS .1. ORGANIC-ACIDS AND ETHANOL, ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG A-FOOD RESEARCH AND TECHNOLOGY, 205(2), 1997, pp. 158-164
The delta(13)C-values of organic acids and their correlations to those
of the sugar and ethanol, respectively, from 57 EU data bank wines of
the Rheinpfalz area (years 1991-1993) and from some of their correspo
nding musts have been determined. In addition to the well established
difference between fermented sugar and ethanol (Delta delta(13)C = -1.
7+/-0.2 parts per thousand), a new constant correlation was found in w
ine for ethanol and citric acid (Delta delta(13)C = +2.4+/-0.4 parts p
er thousand). From this result a fixed delta-value difference for citr
ic acid in wine to the fermented sugar of +0.7+/-0.6 parts per thousan
d can be deduced. The delta(13)C-values of L-malic acid and L-tartaric
acid in must were not altered by the alcoholic fermentation; they sho
uld therefore directly provide access to the delta(13)C-value of the n
atural sugar in must. However, in non-adulterated wines the expected d
elta(13)C-value differences between these acids and ethanol showed uns
atisfactory correlation coefficients. For L-malate this is attributed
to the secondary (partial) degradation of this acid by the malolactic
fermentation; a corresponding correction is envisaged in order to make
L-malate available as an internal standard. As a reason for the unsat
isfactory correlation between L-tartaric acid and ethanol, it is suppo
sed that the time of its maximum biosynthesis period does not coincide
with that of glucose in the grape ripening period.