Quality changes during ripening of plums (Prunus domestica L.)

Quality changes during fruit ripening after the appearance of fruit colour of four Prunus domestica L. plum cultivars, ‘Jojo’, ‘Valor’, ‘Čačanska rodna’ and ‘Čačanska najbolja’, were investigated during 25 or 33 day periods. Fruit samples were analyzed for fruit weight, firmness, soluble solids content, fruit colour, content of sugars (glucose, fructose, sorbitol and sucrose), organic acids (malic, fumaric and shikimic acids), phenolics (neochlorogenic acid, p-coumaroylquinic acid, chlorogenic acid and rutin) and anthocyanins (cyanidin-3-rutinoside and peonidin-3-rutinoside). Ripening resulted in statistically increased fruit weight and soluble solids, decreased fruit firmness, darker colour of fruits, increased concentration of total sugars, decreased concentration of total acids, and increased concentration of anthocyanins. There was no influence of ripening on the content of phenols. The results show significant influences of cultivar on fruit weight, soluble solids content, firmness, fruit colour, concentration of total acids, SUAC index, concentration of total phenols and anthocyanins in European plums.     

Effect of candying on microstructure and texture of plums (Prunus domestica L.)

The plums (Prunus domestica L.) of a specific ‘Green Gage’ variety, “Rainha Cláudia Verde”, are used to produce the candied product “Ameixa d’Elvas”. The candying process consists in boiling the intact plums in water and further immersion in sucrose syrup until 75 °Brix. Scanning electron microscopy of unprocessed plums revealed perfectly turgid parenchyma isodiametric cells with few intercellular spaces and the boiled plums showed a loss of intercellular adhesion of parenchyma cells and ruptures on the vascular strand structure. However, candied plums showed recovery of the turgidity and cell-to-cell adhesion of parenchyma cells. Texture analysis showed that the unprocessed plums had a fairly hard texture, improved by the presence of the skin. Firmness, rigidity, and deformation work had a sharp decrease upon boiling. However, after candying, an increase of firmness and deformation work was observed, also improved by the skin. Microstructure and texture recovery of the candying product suggests the formation of a jam-like structure in the middle lamella region promoted by the syrup. Nevertheless, cell adhesion recovery is limited by the extent of the disruption of the tissues during the boiling process. This is the first report concerning texture and microstructure changes of plums occurring during the candying process.     

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).     

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.     

Effect of candying on cell wall polysaccharides of plums (Prunus domestica L.) and influence of cell wall enzymes

“Ameixa d’Elvas” is a candied plum (Prunus domestica L.) produced by a traditional process, using fruits of a specific ‘greengage’ variety, “Rainha Cláudia Verde”. The candying process consists of boiling the intact plums in water for 15 min and then putting them in sugar syrup, which is successively concentrated until 75 °Brix. Although a loss of intercellular adhesion of parenchyma cells after boiling is observed, candied plums are able to recover their cell-to-cell adhesion, giving a final tissue with a consistency similar to that observed for the fresh fruit. In order to explain this observation, cell wall polysaccharides of plums harvested in two orchards, Vila Viçosa (VV) and Cano (CA), from the same geographic region and at the same stage of ripening, were analysed fresh, boiled and candied. Plum cell walls are composed mainly of pectic polysaccharides and cellulose that, during the boiling step, are degraded and solubilised. Highly esterified pectic polysaccharides undergo gelation inside the fruits in the presence of sucrose, leading to the recovery of the fruit’s consistency. During the candying process diffusion of these methylesterified pectic polysaccharides to the sucrose syrup increase the syrup viscosity. The activity of pectin methylesterase, polygalacturonase, and cellulase of fresh fruits explains the observed higher extension of degradation of cell wall polysaccharides of the CA plum tissues after boiling. This higher degradation seems to prevent the complete recovery of the parenchyma cell structure, which was observed for the less degraded polysaccharides of VV plums.     

Anthocyanins and hydroxycinnamic acids of Lambert Compact cherries (Prunus avium L.) after cold storage and 1-methylcyclopropene treatment

Sweet cherries cv. Lambert Compact were treated with 1-methylcyclopropene (1-MCP) at 0, 180 and 360 nL/L for 2 h at 25 °C and then stored at 2–4 °C in refrigerator. Their quality was measured after 12 days of storage in terms of the contents of total and individual anthocyanins and hydroxycinnamic acids, occurrence of rot, and colour change. Colour change was monitored at three day intervals during storage in the CIE L*, a*, b* colour space. 1-MCP did not retard colour change. The contents of total and individual anthocyanins and hydroxycinnamic acids showed no correlation with the colour behaviour of the cherries. All cherries lost their initial shiny red colour on storage, regardless of the treatment. 1-MCP reduced sweet cherry rot at the highest concentration used (360 nL/L) – only 6% were rotten after 12 days in the refrigerator. This differed significantly (P < 0.05) from untreated fruits and those treated with 180 nL/L 1-MCP which resulted on average in 14 and 20% rot (not statistically different P < 0.05), respectively. The occurrence of rot was shown to be correlated with anthocyanin accumulation, (R = 0.62, P < 0.10). The profile of individual anthocyanins and hydroxycinnamic acids in sweet cherry was not affected neither by cold storage nor 1-MCP treatment.     

Search for suitable maturation parameters to define the harvest maturity of plums (Prunus domestica L.): A case study of candied plums

Plums (Prunus domestica L.) of a greengage variety, from South–East of Portugal, are used to produce a traditional candied product, “Ameixa d’Elvas”, which has a Protected Designation of Origin, recognised by the European Union. To obtain a good texture quality in candied plums, it is necessary to define accurate maturation parameters. Parameters such as the total soluble solids (TSS), titratable acidity (TA), TSS/TA, and pH are not always suitable for this purpose. In order to find a more reliable maturation parameter, plums were collected during the commercial harvesting period, in two orchards, Vila Viçosa and Cano in different years (2003 and 2005). Total polysaccharides (PS) and uronic acids (UA) were quantified in the alcohol-insoluble residues (AIR) of pulp. In all harvests, the content of polysaccharides and uronic acids present in the AIR increased as the maturity of the fruits progressed. To the dataset that comprised the TSS, TA, TSS/TA, pH, PS, and UA measured in these plums, a linear discriminant classifier was applied to obtain a reliable parameter to predict fruit quality upon candying. The models built showed errors of lack of fitness of 0.005% for the content of UA in the AIR and 0.8% for PS, which contrasted with the errors of 17%, 21%, 17%, and 11%, for the TSS, TA, ratio TSS/TA, and pH, respectively. Considering that the variability associated with the content of PS was higher than that observed in UA estimation, and the easy and fast determination of UA, it is proposed that the UA content in AIR be used as a reliable harvesting maturity parameter, complementary to TSS and/or TA, to obtain a high quality candied product. An easy and quick laboratory methodology is proposed for the determination of the UA in plums.     

Phenolic profile and antioxidant activity of highbush blueberry (Vaccinium corymbosum L.) during fruit maturation and ripening

The phenolic profile and quantitative composition of blueberries as well as the corresponding antioxidant activity of blueberries is well documented. Unfortunately, little is reported on the development of phenolic compounds and antioxidant activity during fruit maturation and ripening. In the present study, the total phenolic content and main phenolic compounds of four highbush blueberry cultivars (Vaccinium corymbosum L.) were analyzed at five stages of maturation and ripening. Antioxidant activity was screened with electron spin resonance spectrometry and trolox equivalent antioxidant capacity (TEAC) assay. An adequate picture of phenolic compounds developed during maturation and ripening was determined using HPLC-DAD. Anthocyanins of all varieties increased during successive harvest stages; meanwhile flavonols and hydroxycinnamic acids decreased from unripe green to ripe blue stage of berry ripening. Blueberry antioxidant activity, as well as total phenolic content tended to decrease during ripening.     

Sugars,organic acids,phenolic composition and antioxidant activity of sweet cherry (Prunus avium L.)

Sugars, organic acids, phenolics and anthocyanins in fruits of 13 sweet cherry cultivars: Badascony, Burlat, Early Van Compact, Fercer, Fernier, Ferprime, Lala Star, Lapins, Noire de Meched, Sylvia, Vesseaux, Vigred (red-coloured) and Ferrador (bi-coloured) were quantified by HPLC. Sweet cherry cultivars of different pomological characteristics and different time of ripening were evaluated sensorily. Cultivars were evaluated for their total phenolic content and antioxidant activity. The sum of sugars (glucose, fructose, sucrose and sorbitol) ranged from 125 to 265 g/kg fresh weight (FW) and the sum of organic acids (malic, citric, shikimic and fumaric) ranged from 3.67 to 8.66 g/kg FW. Total phenolic content ranged from 44.3 to 87.9 mg gallic acid equivalents/100 g FW and antioxidant activity ranged from 8.0 to 17.2 mg ascorbic acid equivalent antioxidant capacity mg/100 g FW. The correlation of antioxidant activity with total phenolics content and content of anthocyanins was cultivar dependent.     

Changes in pigment profile and surface colour of fig (Ficus carica L.) during drying

In this study, anthocyanins in three fresh fig varieties (Ficus carica L.) cultivated in Turkey were characterised and quantified by HPLC/DAD and HPLC/MS. In addition, the carotenoid composition of Sar?lop and Sar?zeybek, yellow fig varieties, was determined, and then the ripening‐ and drying‐related changes in carotenoids and surface colour of figs were monitored during conventional sun‐drying. Four different anthocyanins, cyanidin‐3‐glucoside, cyanidin‐3,5‐diglucoside, cyanidin‐3‐rutinoside (major anthocyanin) and pelargonidin‐3‐glucoside, were identified in samples. Lutein, zeaxanthin, β‐cryptoxanthin and β‐carotene were carotenoids in yellow fig varieties. Approximately 80% of carotenoid compounds in yellow fig varieties degraded at the end of drying (i.e. seventh day). L (lightness), a (redness and greenness) and b (yellowness and blueness) colour parameters were measured by Hunter Lab system. Great changes in carotenoid composition and surface colour were observed at ripening stage on tree. A significant reduction in L and b values that refers to browning in figs was made in the first 3 days of drying process.     

Effect of low temperature storage on physical and physiological characteristics of eggplant fruit (Solanum melongena L.)

Eggplant (Solanum melongena L.) is a perishable and chilling-sensitive tropical fruit. The chilling injury (CI) symptoms as well as some physical and physiological implications were studied in eggplants Money Maker No. 2 stored at 0 and 10 °C for 15 days. Eggplants stored at 10 °C were not damaged by temperature, whereas fruit stored at 0 °C suffered CI. Eggplant stored at 0 °C exhibited a decrease in L₀ (lightness) and ΔL (oxidation potential), increase of pH and electrolyte leakage after CI symptoms are manifested. At this temperature, flesh tissue revealed ultrastructural damage. On the other hand, skin from upper fruit section showed more lightness, reddish colouration, and lower content of anthocyanins than the central fruit section at harvest and over the entire storage period at 0 °C. In fruit stored at this temperature and in upper section, changes of anthocyanin content with time were closely proportional to the Chroma evolution (lower content of anthocyanin, lower saturation of colour).     

Maintaining mango (Mangifera indica L.) fruit quality during the export chain

Mangoes are tropical/sub tropical fruit with a highly significant economic importance. Preferable quality attributes include freedom from external damages such as bruises, latex or sap injury and decay, uniform weight, colour, aroma, firmness (with little give away, not soft), shape and size. The fruit is rich in antioxidants and recommended to be included in the daily diet due to its health benefits such as reduced risk of cardiac disease, anti cancer, and anti viral activities. Maintenance of mango fruit quality during the supply chain depends on many aspects including adequate orchard management practices, harvesting practices, packing operation, postharvest treatments, temperature management, transportation and storage conditions, and ripening at destination. Postharvest losses are high during the supply chain due to harvesting fruit at improper maturity, mechanical damage during the whole chain, sap burn, spongy tissue, lenticels discolouration, fruit softening, decay, chilling injury, and disease and pest damage. The aim of postharvest treatments and management practices in the supply chain is to create suitable conditions or environments to extend the storage life and retain the quality attributes, nutritional and functional compositions. This review summarises the available research findings to retain the overall mango fruit quality and to reduce postharvest losses during supply chain by adopting suitable postharvest novel technologies.     

A general method for the instrumental assessment of the colour of tomato fruit during ripening

The colour of subjectively-chosen tomato fruit of three contrasting cultivars at each of five stages of ripeness were measured on a tri-stimulus colour difference meter. The values were introduced into a formula previously developed for calculating objective limits for each ripening stage, but satisfactory separations were not achieved. When the colour components for areas on the side-walls of tomatoes were introduced into a revised formula, good discrimination was achieved between classes of fruit from fairly ripe to fully ripe. Similar measurements carried out on areas near the stylar scar and used with an alternative formula led to efficient separation of less ripe fruit into distinct classes. It is suggested that the revised formula can be applied to any cultivated tomato line except colour mutants.     

Drying characteristics and thermal degradation kinetics of hardness,anthocyanin content and colour in purple‐ and red‐fleshed potato (Solanum tuberosum L.) during hot air drying

Purple‐fleshed potatoes (PFP) and red‐fleshed potatoes (RFP) were dried using hot air. The hardness, anthocyanin content and colour in PFP and RFP during drying were evaluated at 60, 70 and 80 °C. The hardness was characterised by a softening stage in the early drying period, followed by a hardening stage. The times to reach at the transition were 420, 300 and 240 min at 60, 70 and 80 °C, respectively, for PFP, and 480, 360 and 240 min for RFP. However, the moisture content of both PFP and RFP at the transition time was identical at 0.3 (d.b.). The two stages of hardness changes were well described by combining two modified first‐order kinetics models. The activation energy (E_a) for the degradation of anthocyanin in PFP and RFP was 25.12 and 28.43 kJ mol^?1, respectively. The E_a values demonstrated that the thermal sensitivity of PFP was higher than that of RFP.     

Characterization of polyphenoloxidase (PPO) and total phenolic contents in medlar (Mespilus germanica L.) fruit during ripening and over ripening

Characterization of polyphenoloxidase (PPO) enzyme and determination of total phenolic concentrations during fruit ripening and over ripening in medlar (Mespilus germanica L.) were determined. During ripening, PPO substrate specificity, optimum pH and temperature, optimum enzyme and substrate concentrations were determined. Among the five mono- and di-phenolic substrates examined ((p-hydroxyphenyl) propionic acid, l-3,4-dihydroxyphenylalanine, catechol, 4-methylcatechol and tyrosine), 4-methylcatechol was selected as the best substrate for all ripening stages. A range of pH 3.0–9.0 was also tested and the highest enzyme activity was at pH 7.0 throughout ripening. The optimum temperature for each ripening stage was determined by measuring the enzyme activity at various temperatures over the range of 10–70 °C with 10 °C increments. The optimum temperatures were found to be 30, 20 and 30 °C, respectively, for each ripening stage. Optimum enzyme and substrate concentrations were found to be 0.1 mg/ml and 40 mM, respectively. The V_max and K_m value of the reaction were determined during ripening and found to be 476 U/mg protein and 26 mM at 193 DAFB (days after full bloom) – stage 1, 256 U/mg protein and 12 mM at 207 DAFB – stage 2, 222 U/mg protein and 8 mM at 214 DAFB – stage 3. For all ripening stages sodium metabisulfite markedly inhibited PPO activity. For stage 1 of ripening, Cu²⁺, Hg²⁺ and Al³⁺, for stage 2, Cu²⁺ and Hg²⁺, and for stage 3, Cu²⁺, Hg²⁺, Al³⁺ and Ca²⁺ strongly inhibited diphenolase activity. Accordingly, it can be concluded that as medlar fruit ripen there is no significant changes in the optimum values of polyphenoloxidases, although their kinetic parametres change. As the fruit ripening progressed through ripe to over-ripe, in contrary to polyphenoloxidase activity, there was an apparent gradual decrease in total fruit phenolic concentrations, as determined by using the aqueous solvents and water extractions.     

Characterization of New Tart Cherry (Prunus cerasus L.): Selections Based on Fruit Quality,Total Anthocyanins,and Antioxidant Capacity

Tart cherries (Prunus cerasus L.) are rich in anthocyanins and possess high antioxidant activity. The objective of this study was to evaluate six Michigan tart cherry selections for different quality attributes; fruit weight, firmness, total soluble solids (TSS), titratable acidity, instrumental color parameters, total anthocyanins, and antioxidant capacity, determined as Oxygen Radical Absorbance Capacity (ORAC). Generally, significant (p < 0.01) differences were observed across tart cherry selections for fruit weight, firmness, total soluble solids, titratable acidity, and color values. As compared to 13.7°B for Montmorency (control), the TSS contents of all the tart cherry selections were significantly higher; ranging from 15.8 °B in selection 27–10(50) to 20.2°B in Erdi Jubileum. Fruit weight also showed significant differences, which were in the range of 3.95–8.17 g/fruit. In comparison to Montmorency, other tart cherry selections showed significantly higher titratable acidity (1.20–1.41% vs. 1.132%); higher anthocyanins (78.9–391.4 μg/g vs. 33.1 μg/g, as gallic acid equivalent); and higher ORAC values (up to 145.4% more). With respect to cost and better marketability, the results of this study could be useful for the cherry juice/concentrate industry.     

Degradation kinetics and colour of anthocyanins in aqueous extracts of purple- and red-flesh potatoes (Solanum tuberosum L.)

The effect of pH and temperature on the stability and visual colour of aqueous anthocyanin (ACY) extracts from purple- and red-flesh potatoes was evaluated and compared to commercial ACY extracts from grape and purple carrot. Extracts from purple carrot and red-flesh potatoes showed higher stability than grape and purple-flesh potato extracts. Stability to pH (?3) and thermal degradation of extracts (pH 3) followed first-order kinetics. Changes in lightness and hue followed zero-order kinetics, while changes in chroma followed first-order kinetics. Degradation parameters such as t_1/2, k-, D-, z- and Q₁₀-values were determined. Extracts from red- and purple-flesh potatoes at pH 3 showed similar hues to FD&C Red #40 and red cabbage extracts, respectively. The visual colour of both potato ACY extracts was also affected by tinctorial strength. The use of purple- and red-flesh potatoes as a source of natural colorants shows potential use in the pH region around 3.     

Characterisation of cell wall polysaccharide profiles of apricots (Prunus armeniaca L.), peaches (Prunus persica L.), and pumpkins (Cucurbita sp.) for the evaluation of fruit product authenticity

Cell wall polysaccharides were investigated for their suitability as markers for quality and authenticity control of fruit products. For this purpose, the alcohol-insoluble residue (AIR) from several cultivars of apricots and peaches of different harvest seasons, provenances, and stages of ripeness was extracted and subsequently fractionated into acid- and EDTA/alkali-soluble pectins, hemicellulose, and cellulose. Each fraction was analysed for its neutral sugar composition by gas chromatography. In addition, analyses were also carried out on several cultivars of pumpkins because of their potential for use in fraudulent admixtures. Within the respective fruit species, characteristic neutral sugar profiles of the AIR and its fractions were observed, which were found to be independent of the cultivar, harvest season, and provenance. The fruit specific saccharide composition may be used for the differentiation of fruit products devoid of carbohydrate-based hydrocolloids. Furthermore, the isolated hemicellulose may also allow the detection of admixtures of non-specified fruit in complex fruit products, such as jams, spreads, and fruit preparations.     

Chemical changes of three native Turkish hazelnut varieties (Corylus avellana L.) during fruit development

Three native hazelnut varieties from Turkey, namely, Tombul, Palaz, and Badem, were examined for their proximate composition, minerals, and fatty acid profiles, as well as polyphenol oxidase (PPO), peroxidase (POD), and lipase activities during fruit development stages (early stage: ES, middle stage: MS, and harvest stage: HS). Proximate composition varied considerably (dry weight basis) from ES to MS. Fat was the predominant component at all stages and showed increasing trends. Six essential minerals (calcium, iron, magnesium, phosphorus, potassium, and zinc) were analysed (dry weight basis). Consuming recommended daily amount of 42.5 g hazelnut at HS supplies 23.3–25.0% of phosphorus, 11.6–18.1% of magnesium, 7.0–18.9% of iron, 4.9–8.9% of zinc, 5.1–5.7% of calcium, and 5.1–5.3% of potassium for recommended dietary allowances or adequate intake for adults. Significant (P < 0.05) decreasing trends were found in all mineral contents from early development to maturity, with some exceptions. Sixteen fatty acids were identified, among which 18:1ω9 was by far the most predominant one, followed by 18:2ω6, 16:0, and 18:0. As expected, total monounsaturated fatty acids constituted the main group of fatty acids ranging from 75.51 to 81.07% in Tombul, from 78.21 to 82.71% in Palaz, and from 73.69 to 81.65% in Badem through the maturation stages. In contrast, total polyunsaturated fatty acids showed decreasing trends from ES to HS. No significant changes (P > 0.05) were observed in total saturated fatty acids at different maturation stages. Tombul variety had the lowest PPO activity compared to those of Palaz and Badem. Badem showed highest POD activity compared to Tombul and Palaz at three stages of maturation and significant decreases (P < 0.05) in all hazelnut samples were observed in POD activity from ES to HS. No lipase activity was detected in any hazelnut samples at ES and MS, except in Badem at MS. In contrast, lipase activity was detected in all hazelnut samples at HS. These results suggest that some proximate compositions, minerals, and fatty acids gave good indications during fruit development stages, whereas enzymatic activities of PPO, POD, and lipase behaved differently among varieties and fruit development stages.     

Extractable antioxidants and non-extractable phenolics in the total antioxidant activity of selected plum cultivars (Prunus domestica L.): Evolution during on-tree ripening

The purpose of this study was to evaluate the contribution of extractable antioxidants and non-extractable phenolics to the total antioxidant activity (TAA) of plums. Therefore, the antioxidant activity was determined (ABTS assay) in aqueous–organic extracts, as well as in the extraction residues which were a subject of two different acidic treatments to release hydrolysable tannins and non-extractable proanthocyanidins (NEPA). In addition, the changes in TAA during the last week of ripening were investigated. Extractable antioxidants contributed less than 18% to the TAA, considerably higher values of antioxidant activity were associated with hydrolysable tannins and NEPA, suggesting that the antioxidant activity of plums may be underestimated in the literature. The ripening resulted in an increase of TAA up to 38% in excess of the value determined on the first sampling date. TAA showed a similar pattern over the ripening period for all cultivars studied.