Effects of Storage Temperature, Humidity and Duration on Ostrich Fern (Matteuccia Struthiopteris (L.) Todaro) Quality

Storage of Ostrich ferns (fiddleheads) at temperatures above or below 0°C decreased storage life and marketable quality. Percent weight loss, ascorbic acid, bacterial load, yeast and mold loads generally increased and relative water content decreased with increased storage temperature above 0°C and duration. Fiddlehead absolute moisture and ascorbic acid decreased with extended storage at lower storage humidities. Marketable yields decreased with higher storage temperatures, lower storage humidity and extended storage durations. Optimum storage conditions of 0°C and 100% RH provided marketable yields of 95% and 76% after 16 and 32 days, respectively, while fiddlehead storage in water at 0°C for 15 days provided marketable yields of 97%.     

Effects of β‐cyclodextrin addition and farming type on vitamin C,antioxidant activity,carotenoids profile,and sensory analysis in pasteurised orange juices

The effects of organic farming, pasteurisation and addition of β‐cyclodextrin on the content of vitamin C, colour, carotenoids and antioxidant capacity of orange juices were studied. After pasteurisation at 98 °C (20 s) and subsequently storage along 145 days at room temperature (20–25 °C), the loss of vitamin C content was around 30%. The effects of the thermal process on carotenoid were clearly observed in lutein (loss of 16% for organic and traditional 8%) and especially β‐cryptoxanthin (loss of 30%). The colour changes were noticeable after the pasteurisation of orange juice and subsequent storage, with significant decreases being observed in lightness and the coordinate a*, while increases were found for coordinates b*, Hue* and chroma. The antioxidant capacity was 0.075 ± 0.01 and 0.053 ± 0.01 mMT mL^?1 for organic and conventional, respectively, with losses around 40% being found at the end of the storage period. The addition of β‐cyclodextrin caused no significant effects on the parameters under analysis. These data showed that strong thermal treatments, such as pasteurisation, adversely affect the nutritional and sensory quality of orange juices.     

Effect of refrigerated storage on vitamin C and antioxidant activity of orange juice processed by high-pressure or pulsed electric fields with regard to low pasteurization

A better knowledge of the effect of refrigerated storage on the nutritional and antioxidant characteristics of foods processed by emerging technologies with regard to thermal traditional technology is necessary. Thus, freshly squeezed orange juice was processed by high-pressure (HP) (400 MPa/40 °C/1 min), pulsed electric fields (PEF) (35 kV/cm/750 μs) and low pasteurization (LPT) (70 °C/30 s). The stability of vitamin C and antioxidant activity was studied just after treatment and during 40 days of refrigerated storage at 4 °C. The determination of total vitamin C (ascorbic acid plus dehydroascorbic acid) was achieved by HPLC whereas the antioxidant activity was assessed by the measurement of the DPPH• radical scavenging. Just after treatment, all treated orange juices showed a decrease lower than 8% in vitamin C content compared with the untreated one. At the end of refrigerated storage, HP and LPT juices showed similar vitamin C losses (14 and 18%, respectively) in relation to untreated juice, although HP juices maintained better the vitamin C content during more days than LPT juices. Regarding antioxidant activity, after 40 days at 4 °C, differences among treated juices were no significant in terms of antiradical efficiency (AE=1/EC₅₀T_EC50). HP and PEF may be technologies as effective as LPT to retain antioxidant characteristics of orange juice during refrigerated storage.     

The effects of nanoemulsions based on citrus essential oils (orange,mandarin, grapefruit,and lemon) on the shelf life of rainbow trout (Oncorhynchus mykiss) fillets at 4 ± 2°C

This study investigated the antioxidant and antimicrobial effects of nanoemulsions of orange, grapefruit, mandarin, and lemon essential oils on rainbow trout fillets stored at 4 ± 2°C in refrigerator. The results demonstrated that the shelf life of the rainbow trout fillets was determined as 10 days for the control group, 12 days for the tween 80 (surfactant), 14 days for orange and lemon treatment groups, and 16 days for mandarin and grapefruit groups. Nanoemulsions based on essential oils removed the fishy odor and had a positive effect on organoleptic quality. The use of citrus essential oil-based nanoemulsions decreased the values of biochemical parameters and slowed the growth of bacteria compared to the control group. Among all treatment groups, only the control group exceeded the TVB-N limit value on the 12th day of storage. PV and FFA values in fillets treated with mandarin and grapefruit nanoemulsions developed more slowly during the storage period. In addition, the lowest bacteria counts were found in the mandarin and grapefruit treatment groups. It can be concluded that especially mandarin and grapefruit EOs in all citrus essential oils can be recommended for preparing nanoemulsions in the preservation of rainbow trout fillets.     

Comparison of High Hydrostatic Pressure,High-PressureCarbon Dioxide and High-Temperature Short-Time Processing on Quality of Mulberry Juice

Changes of microbial, physicochemical and sensory properties of mulberry juice processed by high hydrostatic pressure (HHP) (500 MPa/5 min), high-pressure carbon dioxide (HPCD) (15 MPa/55 °C/10 min), and high-temperature short time (HTST) (110 °C/8.6 s) during 28 days of storage at 4 °C and 25 °C were investigated. Total aerobic bacteria (TAB) and yeast and mold (Y&M) were not detected in HHP-treated and HTST-treated mulberry juices for 28 days at 4 °C and 25 °C, but were detected more than 2 log₁₀ CFU/ml in HPCD-treated mulberry juice for 21 days at 4 °C and 14 days at 25 °C, respectively. Total anthocyanins were retained after HHP and reduced by 4 % after HTST while increased by 11 % after HPCD. Total phenols were retained by HHP, while increased by 4 % after HTST and 16 % after HPCD. The antioxidant capacity was retained by HTST and HHP and increased by HPCD. Both total phenols and antioxidant capacity were decreased during the initial 14 days but then increased up to 28 days regardless of storage temperature. The value of polymeric color and browning index decreased and a* increased in HHP-treated and HPCD-treated mulberry juices, while HTST-treated mulberry juice had a reverse result. The viscosity of mulberry juice increased in HHP-treated and HPCD-treated juices, while decreased in HTST-treated juice. During storage, total anthocyanins, total phenols, and antioxidant capacity and color in all mulberry juices decreased more largely at 25 °C than that at 4 °C. Better quality was observed in HHP- and HPCD-treated mulberry juices, and a longer shelf life was observed in HHP-treated samples compared to HPCD-treated ones.     

The growth of Propionibacterium cyclohexanicum in fruit juices and its survival following elevated temperature treatments

This study investigated the growth of Propionibacterium cyclohexanicum in orange juice over a temperature range from 4 to 40 degrees C and its ability to multiply in tomato, grapefruit, apple, pineapple and cranberry juices at 30 and 35 degrees C. Survival after 10 min exposure to 50, 60, 70, 80, 85, 90 and 95 degrees C in culture medium and in orange juice was also assessed. In orange juice the organism was able to multiply by 2 logs at temperatures from 4 to 35 degrees C and survived for up to 52 days. However, at 40 degrees C viable counts were reduced after 6 days and no viable cells isolated after 17 days. The optimum growth temperature in orange juice over 6 days was 25 degrees C but over 4 days it was 35 degrees C. The growth of P. cyclohexanicum was monitored in tomato, grapefruit, cranberry, pineapple and apple juices at 30 and 35 degrees C over 29 days. Cranberry, grapefruit and apple juice did not support the growth of P. cyclohexanicum. At 30 degrees C no viable cells were detected after 8 days in cranberry juice or after 22 days in grapefruit juice while at 35 degrees C no viable cells were detected after 5 and 15 days, respectively. However, in apple juice, although a 5 log reduction occurred, viable cells could be detected after 29 days. P. cyclohexanicum was able to multiply in both tomato and pineapple juices. In tomato juice, there was a 2 log increase in viable counts after 8 days at 30 degrees C but no increase at 35 degrees C, while in pineapple juice there was a 1 log increase in numbers over 29 days with no significant difference between numbers of viable cells present at 30 and 35 degrees C. The organism survived at 50 degrees C for 10 min in culture medium without a significant loss of viability while similar treatment at 60, 70 and 80 degrees C resulted in approximately a 3-4 log reduction, with no viable cells detected after treatment at 85 or 90 or 95 degrees C but, when pre-treated at intermediate temperatures before exposure to higher temperatures, some cells survived. However, in orange juice a proportion of cells survived at 95 degrees C for 10 min without pre-treatment and there was no significant difference between numbers surviving with and without pre-treatment. The results from this study demonstrate that P. cyclohexanicum is able to grow in a number of juices, other than orange juice, and able to survive a number of high temperature procedures. Therefore, if initially present in the raw materials P. cyclohexanicum might survive the pasteurization procedures used in the fruit juice industry, contaminate and consequently spoil the final product.     

High hydrostatic pressure treatment and storage of carrot and tomato juices: Antioxidant activity and microbial safety

The application of high hydrostatic pressure (HHP) (250 MPa, 35 °C for 15 min) and thermal treatment (80 °C for 1 min) reduced the microbial load of carrot and tomato juices to undetectable levels. Different combinations of HHP did not cause a significant change in the ascorbic acid content of either juice (P > 0.05). Both heat treatments (60 °C for 5–15 min and 80 °C for 1 min) resulted in a significant loss (P < 0.05) in the free‐radical scavenging activity as compared to untreated samples. HHP‐treated juices showed a small loss of antioxidants (below 10%) during storage. The ascorbic acid content of pressurized tomato and carrot juices remained over 70 and 45% after 30 days of storage, respectively. However, heat treatment caused a rapid decrease to 16–20%. Colour changes were minor (ΔE = 10) for pressurised juices but for heat‐pasteurised samples it was more intense and higher as a result of insufficient antioxidant activity. HHP treatment (250 MPa, 35 °C for 15 min) led to a better product with regard to anti‐radical scavenging capacity, ascorbic acid content and sensory properties (colour, pH) of the tomato and carrot juices compared to conventional pasteurisation. Therefore, HHP can be recommended not only for industrial production but also for safe storage of fresh juices, such as tomato and carrot, even at elevated storage temperatures (25 °C). Copyright © 2007 Society of Chemical Industry     

Determination of Oxygen Solubility in Liquid Foods Using a Dissolved Oxygen Electrode

A rapid method for determining oxygen solubility in foods was introduced. Fructose, glucose, sucrose, orange juice, apple juice, grape juice, grapefruit juice, lemonade, and tomato juice had similar oxygen solubilities at comparable °Brix readings. The equation: In [ppm O₂] = 2.63 ? 0.0179 (°Brix) ? 0.0190 (°C) estimated to within 5% the oxygen solubility of sugar solutions and fruit juices at temperatures between 4°C and 40°C. At likely food concentrations, citric acid, ascorbic acid, and NaCl reduced oxygen solubility by less than 10%. Tests for component interactions were also conducted. There was no measurable synergism or antagonism between fructose, glucose, and sucrose with or without organic acids.     

Composition of Some Organic and Inorganic Compounds in Reverse Osmosis-Concentrated Citrus Juices

Orange, grapefruit and lemon juices were concentrated over twofold in a pilot scale reverse osmosis (RO) process using a commercially available membrane system. Major sugars, acids, vitamin C, aroma volatiles and over 20 minerals were examined in feed, concentrate and permeate streams. Typically, 15–20 aroma compounds were identified in feed juices and concentrates. Compared with less volatile compounds (e.g., ethyl butyrate, limonene), poorer retention during processing was noted for more volatile molecules (methanol, acetaldehyde, ethanol). °Brix of membrane concentrates were orange (25.3°B), grapefruit (25.1°B) and lemon (22.5°B). Vitamin C was rejected efficiently by the membrane. Mineral analyses showed similar elemental contents in feed and concentrate and insignificant concentration in permeate streams.     

Stability of enterocin AS-48 in fruit and vegetable juices

Enterocin AS-48 is a candidate bacteriocin for food biopreservation. Before addressing application of AS-48 to vegetable-based foods, the interaction between AS-48 and vegetable food components and the stability of AS-48 were studied. Enterocin AS-48 had variable interactions with fruit and vegetable juices, with complete, partial, or negligible loss of activity. For some juices, loss of activity was ameliorated by increasing the bacteriocin concentration, diluting the juice, or applying a heat pretreatment. In juices obtained from cabbage, cauliflower, lettuce, green beans, celery, and avocado, AS-48 was very stable for the first 24 to 48 h of storage under refrigeration, and decay of activity was markedly influenced by storage temperature. In fresh-made fruit juices (orange, apple, grapefruit, pear, pineapple, and kiwi) and juice mixtures, AS-48 was very stable for at least 15 days at 4 degrees C, and bacteriocin activity was still detectable after 30 days of storage. Gradual and variable loss of activity occurred in juices stored at 15 and 28 degrees C; inactivation was faster at higher temperatures. In commercial fruit juices (orange, apple, peach, and pineapple) stored at 4 degrees C, the bacteriocin was completely stable for up to 120 days, and over 60% of initial activity was still present in juices stored at 15 degrees C for the same period. Commercial fruit juices stored at 28 degrees C for 120 days retained between 31.5% (apple) and 67.71% (peach) of their initial bacteriocin activity. Solutions of AS-48 in sterile distilled water were stable (120 days at 4 to 28 degrees C). Limited loss of activity was observed after mixing AS-48 with some food-grade dyes and thickening agents. Enterocin AS-48 added to lettuce juice incubated at 15 degrees C reduced viable counts of Listeria monocytogenes CECT 4032 and Bacillus cereus LWL1 to below detection limits and markedly reduced viable counts of Staphylococcus aureus CECT 976.     

Comparative study on shelf life of orange juice processed by high intensity pulsed electric fields or heat treatment

The effects of high intensity pulsed electric fields (HIPEF) processing (35 kV/cm for 1,000 μs; bipolar 4-μs pulses at 200 Hz) on the microbial shelf life and quality-related parameters of orange juice were investigated during storage at 4 and 22 °C and compared to traditional heat pasteurization (90 °C for 1 min) and an unprocessed juice. HIPEF treatment ensured the microbiological stability of orange juice stored for 56 days under refrigeration but spoilage by naturally occurring microorganisms was detected within 30 days of storage at 22 °C. Pectin methyl esterase (PME) of HIPEF-treated orange juice was inactivated by 81.6% whereas heat pasteurization achieved a 100% inactivation. Peroxidase (POD) was destroyed more efficiently with HIPEF processing (100%) than with the thermal treatment (96%). HIPEF-treated orange juice retained better color than heat-pasteurized juice throughout storage but no differences (p<0.05) were found between treatments in pH, acidity and °Brix. Vitamin C retention was outstandingly higher in orange juice processed by HIPEF fitting recommended daily intake standards throughout 56 days storage at 4 °C, whereas heat-processed juice exhibited a poor vitamin C retention beyond 14 days storage (25.2–42.8%). The antioxidant capacity of both treated and untreated orange juice decreased slightly during storage. Heat treatments resulted in lower free-radical scavenging values but no differences (p<0.05) were found between HIPEF-processed and unprocessed orange juice.     

Storage Stability of Lactobacillus paracasei as Free Cells or Encapsulated in Alginate-Based Microcapsules in Low pH Fruit Juices

The main objective of this research effort was to study whether microencapsulation could be a viable alternative to obtain probiotic orange or peach juices. In order to be considered probiotic food, probiotic bacteria must be present in sufficient viable numbers to promote a benefit to the host. The survival and viability of Lactobacillus paracasei L26 in juices over 50?days of storage at 5°C was assessed, evaluating the potential use of encapsulated cells in alginate microcapsules. L. paracasei L26 demonstrated good viability in both orange and peach juices despite the low pH values of both juices. Microencapsulation in alginate, with or without double coating, revealed to be suitable to protect L. paracasei L26 since viable cells were approximately 9 log cfu/g after 50?days of storage at 5°C. In general, the probiotic fruit juices showed a decrease in pH during storage. Glucose and fructose contents as well as citric acid contents decreased during storage, whereas an increase in formic acid was observed. The outcome of this study points to L. paracasei L26 as having promising potential, especially in an encapsulated form, as functional supplements in fruit juices without dairy ingredients due to their tolerance in an acidic environment over 50?days of storage at 5°C. Further studies are warranted to prove the functionality of juices with encapsulated probiotic strains.     

Formation of α-terpineol in Citrus Juices, Model and Buffer Solutions

The formation of α-terpineol from its putative precursors in citrus juice (d-limonene and linalool) was investigated in juice, buffers and model solutions. α-Terpineol content was higher in commercial lemon juice than in orange or grapefruit juices. Its content exceeded its taste threshold of 2.5 mg/L in orange juice stored for 1 month at 35 °C. During storage of homogenized model solutions fortified with d-limonene or linalool, α-terpineol was simultaneously formed and degraded, especially at 45 °C and its formation was strongly dependent on pH. Linalool was a more reactive substrate than limonene for α-terpineol formation; the protonation in linalool was faster than in limonene. However, since there was more limonene than linalool in citrus juices, a-terpineol appeared to have been formed to about the same extent from both precursors.     

Thermal Stability of Ricin in Orange and Apple Juices

ABSTRACT: Ricin is a potent protein toxin that could be exploited for bioterrorism. Although ricin may be detoxified using heat, inactivation conditions in foods are not well characterized. Two brands of pulp-free orange juice and 2 brands of single-strength apple juice (one clarified and the other unclarified) containing 100 μg/mL added ricin were heated at 60 to 90 °C for up to 2 h. With increasing heating times and temperatures the heat-treated juices exhibited decreasing detectability of ricin by enzyme-linked immunosorbent assay (ELISA) and cytotoxicity to cultured cells. Z-values for ricin inactivation in orange juices were 14.4 ± 0.8 °C and 17 ± 4 °C using cytotoxicity assays, compared to 13.4 ± 1.5 °C and 14 ± 2 °C determined by ELISA. Although insignificant differences were apparent for z-values measured for the 2 orange juice brands, significant differences were found in the z-values for the 2 brands of apple juice. The z-values for ricin inactivation in the clarified and unclarified apple juices were 21 ± 4 °C and 9.5 ± 1.1 °C, determined by cytotoxicity assays, and 20 ± 2 °C and 11.6 ± 0.7 °C, respectively, using ELISA. Overall, there were no significant differences between results measured with ELISA and cytotoxicity assays. Ricin stability in orange juice and buffer was evaluated at 25 °C. Half-lives of 10 ± 3 d and 4.9 ± 0.4 d, respectively, indicated that active ricin in juice could reach consumers. These results indicate that ricin in apple and orange juices can remain toxic under some processing and product storage conditions. Practical Application: Ricin is a potent toxin that is abundant in castor beans and is present in the castor bean mash by-product after cold-press extraction of castor oil. U.S. Health and Human Services recognizes that ricin could be used for bioterrorism. This study reports the stability of ricin in apple and orange fruit juices at temperatures ranging from 60 to 90 °C (140 to 194 °F).     

Analysis of sterols: a novel approach for detecting juices of pineapple,passionfruit, orange and grapefruit in compounded beverages

Direct GC/MS analysis of the hexane extracts of fruit juices provides an efficient means for demonstrating that very different sterol patterns exist in the juices of pineapple, passionfruit and the two citrus fruits, orange and grapefruit. Ergostanol and stigmastanol were found to be the sterol markers for pineapple juice, while passionfruit juice was characterised by the presence of an unidentified but unique sterol referred to as compound C. Juices of orange and grapefruit yielded very similar sterol profiles. They were readily distinguished from pineapple and passionfruit juices by a higher stigmasterol/campesterol ratio. Valencene/nootkatone response ratio in the hexane extracts was employed to aid in the differentiation of the two citrus juices. Matrix effects on the determination of sterol and sesquiterpenoid distributions were found to be insignificant. Although natural variation and absolute uniqueness of the sterol profile for each of the four fruit juices were not established due to the relatively small number of fruit samples examined, the results of several compounded beverages clearly point to the potential usefulness of sterol profiles for detecting juices of orange, grapefruit, pineapple and passionfruit in mixed drinks. © 1998 SCI.     

Microbial, Enzymatic, and Chemical Changes During Storage of Fresh and Processed Orange Juice

Microbial, enzymatic, and chemical comparisons were made on orange juice stored at 4°C without pasteurization, with light pasteurization (66°C, 10 sec) directed at vegetative microorganisms, and with full pasteurization (90°C, 60 sec) directed at the heat stable isozyme of pectinesterase. Effects of oxygen-barrier and nonbarrier packaging were also examined. Oxygen-barrier packaging did not benefit unpasteurized juice. However, lightly and fully pasteurized juices in barrier cartons exhibited lower microbial counts, greater ascorbic acid retention, and apparent slowing of cloud loss by the third week of storage. During the first 22 days storage, microbial, cloud, sugar, and ascorbic acid values for lightly pasteurized juice were similar to those of juice receiving full pasteurization.     

SHELF-LIFE OF ASEPTICALLY BOTTLED ORANGE JUICE

In comparison with the regularly thermally processed food product, the aseptically filled ones which receive considerably less heat treatment, is thought to have better taste, texture and color, and exhibit less damage to nutritive properties. In this work the storage stability of aseptically bottled juice stored at 4, 15, 25°C was compared to that of hot filled juice. Criteria for stability were ascorbic acid retention, browning as measured by optical density, tristimulus color reflectance and organoleptic evaluation. It was found that the governing factor of establishing shelf-life was storage temperature rather than the method of filling. The quality parameters for the juices stored at 4 and 15°C were similar for both methods of filling. No difference was found in sensoric evaluations between aseptically filled juices and hot-filled juices stored at the same temperatures after 60 days storage. Immediately after filling the aseptically filled juice was judged slightly better but this difference disappeared rapidly during storage even at 4°C. In all cases juices stored at the lower storage temp, were judged better than those stored at the higher temperature regardless of filling method.     

Effect of refrigerated storage on ascorbic acid content of orange juice treated by pulsed electric fields and thermal pasteurization

Application of pulsed electric fields (PEF) can lead to longer shelf life of fruit juices with minimal product quality loss and good retention of fresh-like flavour. The aim of this study was to evaluate the effect of PEF and conventional pasteurization (90 °C, 20 s) on ascorbic acid content of orange juice, and to assess modifications in ascorbic acid concentration of orange juice stored in refrigeration at 2 and 10 °C for 7 weeks. The ascorbic acid degradation rate was −0.0003, −0.0006, −0.0009 and −0.0010 μs⁻¹ for fields of 25, 30, 35 and 40 kV/cm, respectively. With selected PEF treatment (30 kV/cm and 100 μs) the shelf life based on 50% ascorbic acid losses was 277 days for the PEF-treated orange juice stored at 2 °C, while for the pasteurized juice was 90 days.     

Ascorbic Acid Retention in Orange Juice Stored under Simulated Consumer Home Conditions

Ascorbic acid levels in 13 types of commercially packaged orange juices and a juice drink were monitored over 5–7 days at 4.5°C as stored in the original container. Comparable samples stored in an open plastic container were monitored for comparison. In both cases the average ascorbic acid loss was about 1.5–2% per day. These simulated consumer home conditions showed that juice retained an average of 88% of the original ascorbic acid after 1 wk, and 67% after 2 wk in opened containers stored at typical home refrigerator temperatures.     

The influence of storage temperature and storage time on color stability,retail properties and case-life of retail-ready beef

Steaks from three different muscles were either vacuum or carbon dioxide packed and stored for up to 24 weeks at three different storage temperatures (−1.5, 2, or 5 °C). Following storage, they were displayed for up to 30 h. CIE color coordinates, the oxidative states of myoglobin and pH were measured and muscle color, surface discoloration, retail appearance, and odor were evaluated prior to storage and during display (0, 1, 2, 4, 6, 24 and 30 h), and/or immediately prior to and following display. Prior to display, pH was negatively related to duration of storage, and samples stored at −1.5 °C had the highest and samples stored at 5 °C, had the lowest pH. Perception of muscle color was influenced by duration of storage and display, but lower storage temperatures appeared to produce a stabilizing effect. Both lightness of muscle color and deoxymyoglobin content were apparently not influenced by storage temperature or duration of storage or display. Both oxymyoglobin (OMB) and redness, as defined by CIE a* values, were lost progressively during storage and display, but this loss was progressively lower as storage temperature decreased. Yellowness of muscle color, as defined by CIE b* values, generally decreased as storage was prolonged, and this decrease was observed more quickly at higher storage temperatures. Surprisingly, b* values were not related to duration of display. Both surface discoloration and metmyoglobin (MMB) content increased progressively during storage and display. Samples stored at 5 °C displayed the most surface discoloration, while samples stored at −1.5 °C contained the least MMB and displayed the least surface discoloration. Retail appearance deteriorated progressively during storage in all samples stored at 2 and 5 °C and in samples stored at −1.5 °C, which were displayed for at least 24 h. Retail appearance also deteriorated progressively during display in samples stored at −1.5 and 2 °C for three weeks or longer and in samples stored at 5 °C for 0 to 15 and 24 weeks. In unstored samples, samples to be stored at −1.5 °C generally received the lowest retail appearance scores, but after prolonged storage and display, samples stored at −1.5 °C received higher retail appearance scores than samples stored at 5 °C, particularly when samples were stored for 12 weeks or longer and displayed for 1 h or more. Odor deteriorated progressively during storage when measured both prior to display and after 30 h of display. In samples stored for three weeks or longer, samples stored at −1.5 °C generally received the lowest odor scores and were perceived to have the least prevalent off-odors. Samples stored at −1.5 °C maintained a retail case-life of 30 h, when stored for up to 17 weeks, while samples stored at 2 and 5 °C maintained a retail case-life of 30 h, when stored for only eight and seven weeks, respectively. Consequently, storage life can be more than doubled by storage at subzero temperatures (−1.5 °C).