Colour stability of anthocyanins in aqueous solutions at various pH values

This study focuses on the impact of anthocyanin structures such as 5-glucosidic substitution and aromatic acylation on anthocyanin, colour and stability at various pH values. Two concentrations (0.05 and 0.15 mM) of cyanidin 3-glucoside (1), cyanidin 3-(2″-glucosylglucoside)-5-glucoside (2), and cyanidin 3-(2″-(2^′′′-sinapoylglucosyl)-6″-sinapoylglucoside)-5-glucoside (3) in aqueous solutions were studied at fourteen pH levels between 1.1 and 10.5 during a 98 day period at 10 °C. The three pigments represent the structural variation of many anthocyanins isolated from fruits and vegetables. Colours were expressed by the CIELAB coordinates h_ab, (hue angle), C^* (chroma=saturation), and L^* (lightness), as well as by visible absorption maxima (λ_max) and molar absorption coefficients (ε). Limitations of using only spectral parameters, such as λ_max and ε, to express colour variations, were revealed. Pigment 2 was more unstable than 1 at most pH values, showing lower C^* and higher L^* values after storage for only hours in neutral and weakly acid solutions. Pigment 3 showed higher colour stability than the nonacylated forms at all pH values but pH 1.1, where all pigments retained their colours in the storage period, and in the most alkaline solutions, where all pigments experienced dramatic colour changes. Of potential importance for some food products, in solutions with pH 4.1 and 5.1, 3 maintained nearly the same h_ab, C^*, and L^* values during the whole measuring period (98 days), in contrast to pigments 1 and 2. The hue angle shift towards bluish tones in freshly made samples of anthocyanins with 5-glucosidic substitution, were amplified with aromatic acylation (3) throughout the entire pH range except pH 10.5. The variations in the results emphasizes the importance of structure for anthocyanin properties in fresh and processed fruits and vegetables.     

Effect of Oak Chips on Evolution of Phenolic Compounds and Color Attributes of Bog Bilberry Syrup Wine During Bottle‐Aging

This study investigated the evolution of phenolic compounds of bog bilberry syrup wine during a bottle‐aging process, and further estimated the oak chip treatment on the wine color alteration. The wine was macerated with oak chips (2 or 5 g/L under light or medium toasting level) for 20 d and then bottle‐aged for 6 mo. Results showed that the oak chip treatment significantly increased the content of phenolic compounds and enhanced the copigmented anthocyanin level before aging. It also resulted in an increase on a^* and C^* but a decrease on L^*, b^*, and H^* of the wine. During aging process, a content decrease of total phenol and antioxidant capacity of the wine was observed. Phenolic acids, flavonol glycosides, and anthocyanins reduced the content, whereas flavonol increased the content. Free and copigmented anthocyanin levels decreased, whereas polymerized anthocyanins level increased. This process caused an increase on L^*, b^*, and H^*, but a decrease on a^* and C^*. The oak chip treatment delayed the wine color change and its effect was mainly depended on the addition amount. Partial least square regression revealed that flavonol glycosides, phenolic acids, and anthocyanins displayed a positive correlation with L^*, b^*, and H^*, but a negative correlation with a^* and C^*. Quercetin‐3‐O‐glucuronide, myricetin‐3‐O‐galactoside, chlorogenic acid, and quercetin exerted a more important effect on the color alteration in wine.     

Colour stability of canned strawberries using black carrot and elderberry juice concentrates as natural colourants

Besides texture degradation and aroma loss colour fading and browning of processed fruits, in particular strawberries, displaying comparatively low amounts of non-acylated anthocyanins, still pose a serious problem. Therefore, in the present study the colour of texture-improved canned strawberries was stabilised using commercial concentrates from black carrots and elderberries as natural colourants. CIE L ^* a ^* b ^* values of the fruit surface and of the brine solutions were monitored over a period of 24 weeks under light exposure. Furthermore, the contents of individual anthocyanins were analysed by HPLC-DAD. The colour of the processed control fruits (without added colourant) was unacceptable even at the beginning of the storage. Their anthocyanin contents were reduced by more than 85% at the end of the storage period. In contrast, the colour of canned strawberries containing black carrot and elderberry anthocyanins was significantly improved. Colour difference values ΔE ^* of black carrot-coloured strawberries were found to be smaller than those of the samples containing elderberry concentrate as a colourant. This could be ascribed to the presence of acylated anthocyanins in the first exhibiting exceptional storage stability, while all non-acylated pigments were degraded. The chill brining process for fruit firming markedly affected pigment stability, which can be attributed to enzymes that are still active at cold storage conditions.     

Changes of anthocyanins and hydroxycinnamic acids affecting the skin colour during maturation of sweet cherries (Prunus avium L.)

The content and relative amounts of anthocyanins and hydroxycinnamic acids (HCA) were determined in local sweet cherries (cultivar Petrovka) at 7 stages of maturity, by means of high performance liquid chromatography (HPLC), and compared to instrumentally assessed skin colour of the same sweet cherries. Skin colour of harvested samples was measured using the CIE L^*,a^*,b^* system. The contents of neochlorogenic and 3′-p-coumarylquinnic acids decreased with no significant change in ratio during ripening, except for the first 4 days of maturation, when the ratio changed due to increased content of neochlorogenic acid. The linear increase of total anthocyanins during maturation was observed without the trend of stabilization in the final stages of maturity. The colour change of Petrovka during maturation was influenced by the increase of total anthocyanins, consisting mostly of cyanidin-3-rutinoside and cyanidin-3-glucoside (97-98% of the total). The chroma and L^* values appeared to be optimal indicators of anthocyanin accumulation during maturation, and better than the a^* value and hue angle. The accumulation of anthocyanins from 507.1 to 1150.9 mg of cyanidin-3-rutinoside/kg of fresh weight (FW) during the second half of maturation caused the formation of a new colour cast of Petrovka, which influenced the decrease of redness and colour intensity, as recognized by CIE L^*,a^*,b^* colour space.     

A colorimetric study of oenin copigmented by procyanidins

A colorimetric method was used to analyse the influence of procyanidin structure on colour changes of malvidin 3‐O‐glucoside (oenin) solution resulting from copigmentation. The study was performed in hydroalcoholic citrate/phosphate buffer solution (120 g L^?1) at pH 3.6 and ionic strength 0.2 mol L^?1. Chromatic L*, a* and b* coordinates (CIELAB, D65/10° illuminant/observer condition) obtained from spectral curves recorded between 360 and 830 nm allowed the calculation of lightness L*, chroma C* and hue angle h_ab. In general, addition of copigment induced colour enhancement (loss of lightness and increased chroma). The prevailing parameters affecting colour changes were lightness and chroma for monomers and lightness and hue for procyanidins B5 and B8 (C4–C6 dimers). A small blueing effect was observed only for catechin monomer‐copigmented solutions. For procyanidin copigments, as the structural complexity of the copigment increased, the hue angle moved to yellower values. The ester gallate of dimer B2 produced the strongest modification of colour attributes of oenin solution. Copyright © 2006 Society of Chemical Industry     

Protein changes after irradiation and ice storage of horse mackerel (Trachurus trachurus)

Anthocyanin-rich concentrates from different fruits can be used as natural food colourants. The pigments' stability is comparatively low and dependent on the composition of food matrices. Food ingredients relevant for soft drinks, jelly fruits and salad dressings were tested in model systems regarding their influence on the colour stability of elderberry and black currant concentrate determined by colour measurement (CIE L ^* a ^* b ^*). In aqueous solutions food-grade organic acids and salt were found to influence anthocyanin stability: colour stability increased with increasing pK _a of acids and decreased with increasing salt concentrations. This may be attributed to altered solvation characteristics of aqueous solutions. A stabilizing influence was found for sugars presumably by reducing water activity. However, when heat treatment was applied, e.g. in the production of hydrocolloid gels, fructose was shown to accelerate anthocyanin decay due to the formation of sugar degradation products. Comparing hydrocolloids, alginate was shown to increase colour stability in aqueous solution and pectin displayed overall highest colour stability in a gel model system, suggesting that polyuronic acids may improve anthocyanin stability by intermolecular association.     

Enzymatic vegetable extract with bio‐ active components: Influence of fertiliser on the colour and anthocyanins of red grapes

BACKGROUND: The obtention and physicochemical characterization of an enzymatic vegetable extract (EVE) from agroindustrial wastes by a proteolytic extraction is described. The main components of EVE are nitrogen (peptides and free amino acids) and phytohormones (auxins, gibberellins, cytokinins), as functional components. The effect of EVE as fertilizer/biostimulant on several parameters of red grapes, such as colour and anthocyanins, was also evaluated. RESULTS: Its application induced high anthocyanin content with the specific induction of petunidin. Tristimulus colorimetry was applied in order to study the colour of musts. Grape juice with significant and perceptible differences in colour characteristics was obtained using EVE. The colour points were located around redder hues (h_ab) on the (a*b*)‐plane and lightness (L*) was lower. CONCLUSION: The fertilization with biostimulant shows a promising future in the functional plant nutrition linked with an increase in the organoleptic and quality food parameters. Copyright © 2007 Society of Chemical Industry     

Effects of dietary humate supplementation to broilers on performance,slaughter, carcass and meat colour

BACKGROUND: This experiment was designed to examine the effect of dietary humate supplementation primarily on pH and colour parameters of carcasses, breast fillets and drumsticks and, secondarily on performance and carcass characteristics in broilers. RESULTS: A total of 240 male broiler chicks (Ross‐308) were randomly allocated to four dietary treatments varying in supplemental humate level (0, 0.1, 0.2 and 0.3% for H₀, H₁, H₂ and H₃). Dietary humate supplementation did not affect performance traits and slaughter, hot carcass weights and yields. Carcass‐related variables (pH, L*, a*, b*, H* and C*) were responsive to the dietary treatments. The L*, a*, b*, and C* values for drumstick muscles were higher than those for breast muscles. Except for the L* value, meat colour parameters changed due to packaging. The a* value was higher and b* value was lower for vacuum packaged breast and drumsticks than for those aerobic packaged. Storage period affected colour parameters; while L*, b*, H* and C* values were higher for drumstick skin than for drumstick meat; the a* value was greater in drumstick meat than in skin. CONCLUSION: pH and colour parameters of carcasses, breast fillets and drumsticks of broilers were improved by dietary humate supplementation. However, responses of broiler performance and slaughter and carcass characteristics were minimal. Copyright © 2008 Society of Chemical Industry     

Effect of the time of cold maceration on the evolution of phenolic compounds and colour of Syrah wines elaborated in warm climate

The effect of different cold maceration times on Syrah red wines from warm climate has been evaluated. Differential colorimetry and tristimulus colorimetry were applied to colour data at different points of the vinification stage. Virtually, all the phenolic compounds showed significantly higher content in cold macerated wines, even more when longer contact time was used. Long cold macerated (LCM) wines had the significantly (P < 0.05) highest chroma values (C*_ab) and lowest of lightness (L*) and hue (h_ab). Unexpectedly, wines submitted to short‐time cold maceration (SCM) presented the lowest chroma values, even significantly inferior to that observed in traditional macerated (TM) wines. Moreover, colour changes (ΔE*_ab) between TM and SCM were mainly quantitative (%Δ²L and %Δ²C), whereas they were also qualitative when compared TM with LCM (%Δ²C and %Δ²H). Cold maceration in warm climates characterised by common colour losses must be carefully employed because undesirable consequences on colour may occur.     

The quality of cold-smoked Atlantic salmon (Salmo salar) as affected by salting method, time and temperature

The effects of temperature (4 and 10–12 °C) and time (6, 12 and 24 h) on colorimetric parameters (Commission International de l'Eclairage (CIE) L*a*b*), carotenoid concentration, salt content and yield were investigated in brine (saturated or 50% saturation) and dry salted fillets of cold‐smoked Atlantic salmon (Salmo salar). Lightness (L*), yellowness (b*), hue (H_ab) and chroma (C*) values were lower at 10 than 4 °C (P < 0.01), whereas redness (a*) was unaffected. L* increased (P < 0.05) and a*, b*, H_ab and C* values dropped when salting time was increased (P < 0.001). Astaxanthin concentration of brine‐salted fillets decreased with increasing salting time (P < 0.05), but was unaffected by salting temperature. Increasing salting time affected colour negatively. The salt content of dry salted fillets increased with temperature and salting time. The process yield was unaffected by temperature and decreased with salting time. In conclusion, the cold smoking process is more important for variation in quality parameters than the salting process.     

The high ascorbic acid content is the main cause of the low stability of anthocyanin extracts from acerola

Acerola is considered to be one of the best natural sources of ascorbic acid (AA) and, for this reason, the influence of this component on the stability of anthocyanins from acerola extracts was determined and compared to those from açai, which have no detectable AA. The addition of three different levels of AA to the solution of açai anthocyanins resulted in a 110-fold increase in the degradation rate (k_obs) at the highest fortification level (276 mg/ml). The fact that the flavonoid concentration of the açai anthocyanin extract was 10 times higher than that of the acerola was probably responsible for the three times higher stability of the AA-fortified açai system compared to the acerola system, both at the same AA concentration and similar total polyphenol levels. The higher the level of AA addition to açai anthocyanin solutions, the greater was the colour fading, indicated by increase of L^∗ and decrease of a^∗ and C^∗ values.     

Possibilities of enhancing the colour of egg yolk

BACKGROUND: This study attempts to compare two possibilities of enhancing the colour of egg yolk. One of them is based on the ecological rearing of laying hens on natural green grass whereas the other uses a feeding dose supplemented with natural pigments in laying hens reared in individual cages. Is it possible to distinguish these two technologies using yolk colour determination in the CIELAB system? RESULTS: Yolk colour parameters such as L*, a*, and b* in the group of grazed hens are significantly different (α = 0.001) from those observed in hens reared in cages. The yolk colour shows a darker, redder and more yellow colour. The greatest difference was seen in the red colour parameter, a*, that increased more than twice. Visually, this means a shift towards a more orange colour. Compared to grazing in the meadow (ΔE* = 13.257), the addition of artificial pigments in the feed resulted in a more significant increase in the parameter ΔE* (CIE total colour difference), with the greatest value of ΔE* being observed with the use of both pigments (ΔE* = 24.265). CONCLUSION: Grazing increases the parameter a* whereas the values of the parameter C*_ab remain relatively low. The parameter ΔE* is significantly lower in the case of grazing as compared to the supplementation of the feed with pigments. However, colourity parameters cannot be used as a specific standard to identify a particular grazing technology as their values vary during the laying period. Copyright © 2011 Society of Chemical Industry     

Colour effects of co-pigmentation of anthocyanins revisited—2.A colorimetric look at the solutions of cyanin co-pigmented byrutin using the CIELAB scale

Spectral measurements (380–780 nm) were performed on 224 model solutions of cyanin co-pigmented by the flavonol rutin at pH between 2.5 and 5.5. The colour of the solutions was expressed as colorimetric co-ordinates in the CIELAB scale using the L^* (lightness) C^* (chroma) and h (hue angle) notation (for the D65/10° CIE Illuminant/Observer condition). Contrary to previous reports, all the most intensely co-pigmented solutions, although exhibiting the strongest bathochromic of their λ_max, did not displayed the bluest hues; an inverse, i.e. yellowing, effect was observed in the co-pigmented solutions at the lowest cyanin concentrations. The hyperchromic effect of co-pigmentation always caused a decreasing lightness of the solutions coupled with either an increasing or a decreasing chroma for those at low or high pigment concentrations respectively. Based on the amplitude of total colour CIELAB differences (ΔE*) at each co-pigment to pigment ratio, the most intense effects of co-pigmentation were observed at pH 3.5, except for the solutions at the highest pigment content (pH 4.5); the evolution of colour differences at increasing co-pigment to pigment ratios at pH between 2.5 and 5.5 are discussed. Colour differences calculations also showed that the maximum colour steps at successive increasing co-pigment to pigment ratios were observed at low values (0.5 or 1:1) in the most coloured solutions and at the highest values (up to 8–16:1) in the less coloured ones. In describing the colour effect of co-pigmentation on anthocyanins, the discrepancies found between the results of the present colorimetric approach and those previously reported based on spectral data at the λ_max only are discussed. Only the first one—by considering the spectral variations over the complete range of visible wavelengths and using the psychometric correlates of the three attributes of colour specified in the CIELAB system—correctly describes the colour variations as these are perceived by the human eye.     

Thermal degradation kinetics of anthocyanins and visual colour of Urmu mulberry (Morus nigra L.)

Urmu mulberry (Morus nigra L.) juice was concentrated from 15.02 to 45.20 °Brix by rotary vacuum evaporator at 40 °C. The objectives of this study were to determine the titratable acidity, soluble solid content, antioxidant capacity, total monomeric anthocyanins and total phenolic matter in prepared concentrate, to investigate the thermal degradation kinetics of anthocyanins and Hunter colour parameters (L^∗, a^∗, b^∗) and total colour difference (TCD^∗) and to develop a relationship between visual colour and anthocyanin during thermal processing at 60, 70 and 80 °C. Monomeric anthocyanin degradation showed a first order reaction kinetics. The zero order, first order and a combined kinetics model were applied to the changes in Hunter colour parameters (L^∗, a^∗ and b^∗) and total colour difference (TCD^∗). All colour parameters followed an apparent combined kinetics model. The degradation of anthocyanins showed positive correlation with a^∗, b^∗ and L^∗ and negative correlation with TCD^∗.     

Effect of vacuum frying on main physicochemical and nutritional quality parameters of pineapple chips

BACKGROUND: Slices of MD‐2 pineapple hybrid were vacuum fried at 24 kPa according to a central composite experimental design that simultaneously varied frying time (6.3–7.7 min) and temperature (106.3–117.7 °C). Major physicochemical and nutritional quality factors were measured and modelled using a second‐order polynomial equation. RESULTS: Moisture content, water activity a_w, colour parameters L*, C* and H* and total vitamin C content decreased while total phenolic content and dehydroascorbic acid content increased with increasing frying time and temperature. Oil content, hardness and hydrophilic antioxidant capacity reached minimum values near the centre of the experimental field. By superimposing contour curves, it was determined that processing conditions of 6.9 min frying time and 112 °C frying temperature produced pineapple chips with a golden colour (L*≥ 60, C*≥ 50, H*≥ 80), an a_w of less than 0.29, a moisture content of about 4% and a hardness of less than 1.9 N, giving rise to a crispy texture. Oil content was about 20% (d.b) and residual total vitamin C content (～90 mg per 100 g wet basis (w.b.)) was high. Phenolic compound content was about 150 mg gallic acid equivalents per 100 g w.b. and antioxidant capacity was around 22 µmol Trolox equivalents g^?1 w.b. CONCLUSION: Vacuum frying is a dehydration process that produces healthy fruit snacks which partially preserve the fruit's original colour and nutritional compounds and have a high hydrophilic antioxidant capacity. Copyright © 2008 Society of Chemical Industry     

Effects of pH,sulphur dioxide,alcohol content,temperature and storage time on colour composition of a young Portuguese red table wine

In a young Portuguese red table wine (Douro Valley) a significant relationship between the colour composition (anthocyanins, polymeric pigment, colour density) and five parameters (pH, SO₂, alcohol, temperature, time of storage) were found. Higher temperature increased the loss of individual and total anthocyanins (as measured fay HPLC) during the ageing, while the wines with higher SO₂ content contained a greater amount of anthocyanins. Malvidin 3-glucoside acetate was the only anthocyanin not affected by the SO₂ content, but its concentration was related with the interaction term (time of storage × SO₂ content). Peonidin and malvidin 3-glucoside-p-coumarate were the two anthocyanins affected by the quadratic term of temperature. Three different groups of equations corresponding to the three different states of the glucoside moiety were found. The polymeric pigment absorbance increases daring conservation and with higher temperature, while the pH and SO₂ content decreased the polymeric pigment formation. The colour density of the experimental wine was related significantly to the changes of the coloured anthocyanins and to the polymeric pigment content.     

Effect of ripeness and postharvest storage on the evolution of colour and anthocyanins in cherries (Prunus avium L.)

The relationship between colour parameters and anthocyanins of four sweet cherry cultivars, Burlat, Saco, Summit and Van was studied. The colour (L^∗, a^∗, b^∗, chroma and hue angle parameters) and anthocyanins were analysed during two different years at two different ripening stages (partially ripe, and ripe, respectively). The cherries were analysed at harvest and after storage at 1.5 ± 0.5 °C and 15 ± 5 °C for 30 and 6 days, respectively. The colour was measured by tristimulus colourimetry (CIELAB system) directly on the fruits, while anthocyanins were quantified by HPLC-DAD analysis on methanolic extracts of freeze-dried samples of the fresh cherries and on the differently stored cherries. L^∗, chroma, and hue angle values were always lower for the ripe than for the partially ripe cherries. All of the cultivars were found to contain cyanidin-3-rutinoside and cyanidin-3-glucoside as the major anthocyanins. The total anthocyanin content in fruits of the different cultivars varied in the order Burlat > Saco > Van > Summit. The concentration of anthocyanins increased at both temperatures of storage in both ripe and partially ripe cherries, but the extent of increase varied among cultivars. Cherries stored at 15 ± 5 °C showed higher reduction of L^∗, chroma and hue angle than fruits stored at 1.5 ± 0.5 °C. L^∗, a^∗, b^∗, chroma and hue angle correlated negatively (P < 0.001) with the total anthocyanins levels, but not with the total phenols. These results show that chromatic functions of chroma and hue correlate closely with the evolution of colour and anthocyanins levels during storage of sweet cherries and indicate that colour measurements can be used to monitor pigment evolution and anthocyanin contents of cherries (and vice versa).     

Comparative effect of red yeast rice (Monascus purpureus), red beet root (Beta vulgaris) and betanin (E‐162) on colour and consumer acceptability of fresh pork sausages packaged in a modified atmosphere

Fresh pork sausages containing natural colorants, red yeast rice powder (Monascus purpureus; Frame^®) or a crude red beet root (Beta vulgaris) juice or commercial betanin (E‐162), at different concentrations, were packaged in an atmosphere containing 80% O₂ and 20% CO₂ and stored in the dark for 20 days. The following parameters were measured at 4 day intervals: instrumental colour (CIE L*, a*, b*, a*/b*, C* and h*), reflectance spectra, sensory discoloration (trained panel) and acceptability and willingness to purchase (habitual and non‐habitual consumer panels) under two different lighting displays (standard fluorescent and Promolux^® lamp). The use of colorants improved the colour properties of fresh pork sausages. Sausages with red yeast rice, red beet root juice and betanin had lower L* and h* and higher a* and a*/b* values than control samples. The colour properties of sausages with red beet root were the closest to control sausages, while sausages with red yeast rice had significantly lower b* values. Both natural colorants and betanin protected sausages from discoloration and extended acceptability and willingness to purchase by about 4 days, according to evaluation by habitual consumers under two different types of lighting display. Therefore, red beet root juice may be envisaged as the most suitable natural colorant for use in fresh pork sausages. Copyright © 2005 Society of Chemical Industry     

CIELAB coordinates in response to berry skin anthocyanins and their composition in Vitis

Abstract: Berry skin color OIV index, anthocyanin composition, and content of 78 grape cultivars were surveyed using a CIELAB system and high‐performance liquid chromatography (HPLC)‐mass spectrometry (MS) coupled with photodiode array detection. There were high correlations between L*, b*, and color, while a* was not a representative parameter. L* and b* values declined as berry skin color OIV became darker, and a* increased as berry skin color OIV became darker in pink and red grape cultivars only. The composition and content of anthocyanins varied widely among the cultivars. Total anthocyanins and types of anthocyanins were significantly correlated with color OIV parameters. Through multiple linear regression analysis, cyanidin derivatives had a positive effect on values of L* and b*. Delphinidin derivatives had positive effects on the value of a*. The CIELAB system gave good results for differentiation of grape berry skin color OIV.     

Effect of sulphur dioxide and must extraction on colour,phenolic composition and sensory quality of red table wine

Red wines were made during 1992 from Vitis vinifera var Roriz grapes using a high and a low level of extraction and three levels of total sulphur dioxide (0, 75 and 150 mg SO₂ kg⁻¹). From this single experiment, the effects of total SO₂ and extraction on anthocyanin composition and colour were observed by HPLC, spectrophotometry and tristimulus colorimetry. High extraction produced a wine with more total pigments and total phenols than low extraction and increased the amount of organic acids extracted during fermentation. More anthocyanins were extracted with increasing SO₂ levels. On maturation, all wines lost colour and increased in brownness. Wines made without SO₂ browned more than the wines made with SO₂. The anthocyanins normally present in wines were all rapidly lost to trace levels at 24 months. Vitisin A, a more stable and highly coloured anthocyanin than malvidin 3-glucoside, showed a slower decrease in concentration than malvidin 3-glucoside and contributed significantly to the wine colour during aging. At the first analysis, the wines made without SO₂ had a higher percentage colour due to polymers than the wines made with SO₂. Polymerisation progressed during maturation, although the initial differences were maintained. Sensory analysis after 6 and 18 months storage by expert tasters revealed differences mainly related to the colour attributes, indicating that when wines are made using modern hygienic techniques, total SO₂ has a negligible effect on aroma and flavour attributes. © 1998 Society of Chemical Industry.