Chilled storage life of hot-boned, pre-rigor, salted minced beef

Pre-rigor beef mince with 2% added salt was stored under CO₂ at −1.5 °C (A). The same mince with 100 ppm sodium nitrite was stored under CO₂ at 5 °C (B) and −1.5 °C (C), and under vacuum at −1.5 °C (D). Microbiological and sensory analyses were carried out for up to 21 weeks. Indicative storage life was taken as the time for microbial numbers to reach 10⁷ colony forming units per g. Mince stored under regimes B or D attained these numbers by 6 and 14 weeks, respectively; mince stored under regimes A and C had not attained these numbers by the end of the storage trial. Mince stored at 5 °C developed storage flavours of sufficient intensity to be detectable by consumers by 9 weeks storage. In general, the other minces did not develop unacceptable levels of storage or off flavours. Over 90% of the added sodium nitrite had disappeared after 10 weeks of storage, partly through conversion to sodium nitrate. Mince pH was not affected by the storage conditions and remained at about 6.0. The water holding capacity of the pre-rigor mince deteriorated during prolonged storage.     

The storage life of chilled pork packaged under carbon dioxide

Pork cuts of longissimus dorsi muscle with overlaying fat and skin were packed under vacuum in film of low oxygen transmission rate, or under CO₂ in gas impermeable aluminium foil laminate. Cuts were stored at +3 or −1·5°C. Vacuum packaged cuts were grossly spoiled by Brochothrix thermosphacta after 2 weeks' storage at 3°C and after 5 weeks at −1·5°C. Cuts packaged under CO₂ were grossly spoiled by B. thermosphacta after 5·5 weeks' storage at 3°C. Growth of B. thermosphacta was suppressed when CO₂ packaged cuts were stored at −1·5°C. At that temperature, slow growth of enterobacteria was detected after a lag of about 18 weeks. The enterobacteria caused gross spoilage of an increasing proportion of cuts between 18 and 26 weeks. Muscle tissue with pale, soft, exudative (PSE) characteristics tended to lose colour after long storage periods, apparently because of loss of myogglobin with exudate. Until spoilage, the eating qualities of pork appeared little affected by prolonged storage.     

The display life of retail-packaged beef steaks after their storage in master packs under various atmospheres

Beef strip loins were divided into four portions. One portion of each loin was vacuum-packaged and then stored at −1·5°C. The other portions were each divided into three steaks, which were retail-packaged. The retail packs were master-packaged under atmospheres of N₂, CO₂, or O₂ + CO₂ (2 : 1, v/v) and then stored at 2°C. Product was assessed after storage times of up to 60 days. At each assessment, a vacuum pack and a master pack of each type, each containing product from the same loin, were withdrawn from storage. The vacuum-packaged product was cut into three steaks, which were retail-packaged. The newly prepared retail packs and those from the master packs were displayed in a retail cabinet, at air temperatures that averaged between 3 and 5·7°C, and were assessed twice daily until the product was judged to be unacceptable. When first assessed, steaks cut from vacuum-packaged product were generally considered desirable, with little metmyoglobin in the surface pigment, although the edges of same steaks were discoloured. Steaks stored under N₂ or CO₂ for 4 days or less were only slightly desirable at best, with metmyoglobin forming relatively large fractions of the surface pigment. However, after storage under N₂ or CO₂ for 6 days or more, metmyoglobin fractions were low, and the steaks bloomed to a desirable red colour. Steaks stored under O₂ + CO₂ had lower metmyoglobin fractions, and were desirable after storage for up to 8 days. However, the fractions of metmyoglobin increased, and steaks were judged to be less desirable after longer storage times. Steaks stored under O₂ + CO₂ for 20 days were unacceptable. After storage, the numbers of bacteria on steaks from vacuum packs and N₂, CO₂, and O₂ + CO₂ atmospheres were, respectively, <10⁴, <10⁶, <10⁵, and <10⁴ CFU/cm². The flora from steaks stored under CO₂ were composed wholly of lactic acid bacteria. Other flora were dominated by lactic acid bacteria, but contained fractions of enterobacteria and/or Brochothrix thermosphacta.

The appearance of product from vacuum packs generally was unacceptable after 72 h of display. The display life of steaks stored under N₂ or CO₂ was shorter than that of the product from vacuum packs when product was stored for 2 days or less, or 46 days or more. After other storage times, the product from vacuum packs or master packs with N₂ or CO₂ atmospheres had a similar display life. The display life of product stored under O₂ + CO₂ was similar to that of product from vacuum packs or CO₂ or O₂ + CO₂ was similar to that of product from vacuum packs after storage times of 8 days or less but was shorter after storage times of 12 or 16 days. The flora on displayed product from vacuum packs or CO₂ or O₂ + CO₂. atmospheres did not attain the maximum number of 10⁷ CFU/cm². and the product did not develop off-odours of microbial origin. However, numbers of 10⁷ CFU/cm² were approached or attained during display of product stored under N₂ for 28 days or longer, and some of that product developed moderate off-odours. It then appears that, under temperature regimes that are common in commercial practice, retail-packaged strip-loin steaks with a display life of 2 days or longer can be obtained from master packs after storage periods of up to about 2, 4, or 7 weeks, respectively, with master-pack atmospheres of O₂ + COPin2 (2 : 1, v/v), N₂, or CO₂.     

Influence of packaging method and length of chilled storage on microflora, tenderness and colour stability of venison loins

Sections of venison loins (LD) weighing approximately 300 g from 12 red deer (Cervus elaphus) were packaged using four packaging methods: (a) vacuum packaging, (b) CO₂ flushed using a nylon containment film (CO₂-Nylon), (c) CO₂ flushed using an ultra-high barrier containment film (CO₂-UHB), and (d) CO₂ flushed using an aluminium foil laminate containment film (CO₂-Foil) and stored for 1, 6, 12 and 18 weeks at 0°C. Meat pH values were lower in all CO₂ flushed meat packages (P<0·05) than in vacuum packaged meat. Lactic acid bacteria and total anaerobic counts increased over storage time in all packages regardless of treatment up to values of log₁₀ 7·8 and 7·6 g⁻¹, respectively. Tenderness tended to increase as meat was stored for up to 18 weeks. Colour scores taken during simulated retail display indicated that colour deteriorated more rapidly when meat was stored for 12 and 18 weeks than for 1 and 6 weeks. Vacuum packaging and gas flushing (CO₂-Foil) resulted in higher initial colour scores than venison packaged in the CO₂-Nylon or CO₂-UHB materials. Venison stored for 18 weeks also exhibited a higher proportion of packages containing off odours, lower flavour desirability and flavour intensity scores as well as higher off flavour scores than meat stored for shorter times. The implications of these effects are discussed. Although there were few significant differences in microbial growth and sensory characteristics due to packaging method or containment film, vacuum packaging appeared to be the most economic and produced meat of better colour stability.     

Identification of halothane genotypes by calcium accumulation and their meat quality using live pigs

The three halothane genotypes (NN, Nn, and nm) were identified by measuring the capacity for Ca²⁺ accumulation by sarcoplasmic reticulum in whole muscle homogenate preparations of M. longissimus dorsi with a Ca²⁺ specific electrode at 35°C. Significant differences (P < 0·001) in deterioration (%) of Ca²⁺ accumulation, 12% for NN, 35% for Nn, and 81% for nn pigs, were observed after ageing the whole muscle homogenate preparations for 24 h in ice.

Predictions of meat quality in live pigs (n = 34) based on the values for water-holding capacity, assessed as fluid (g/0·5 g wet wt LD), and pH (fluid) by using small biopsy LD samples (Cheah et al. 1993) were performed on all the halothane genotypes. The halothane genotype NN (n = 11) showed a fluid value of 0·37 ± 0·01 and a pH (fluid) value of 6·62 ± 0·03 as compared with 0·61 ± 0·02 and 5·84 ± 0·04, respectively, for the halothane genotype nn (n = 13). The Nn pigs (n = 10) showed fluid (0·49 ± 0·03) and pH (fluid) (6·19 ± 0·11) values between those values observed for the two homozygotes (NN and nn). Predictions of meat quality in live pigs from biopsy LD muscles were confirmed from assessments on post-mortem LD muscles based on pH₁ and fibre optic probe (FOP) measurements.

The extent of deterioration (%) in Ca²⁺ accumulation showed high correlations with fluid (r = −0·861) and pH (fluid) (r = −0·831) in the biopsy LD samples, and with pH₁ (r = 0·663), FOP (r = −0·812), and drip (%) loss (r = −0·777) in the post-mortem LD samples.     

Design, fabrication, and testing of a returnable, insulated, nitrogen-refrigerated shipping container for distribution of fresh red meat under controlled CO2 atmosphere

In today's market, fresh red meat is cut and packaged at both the wholesale and retail level. Greater economies could result if the wholesaler prepared all consumer cuts centrally, but the short storage life of meat limits distribution. Use of CO₂-controlled atmosphere, master packaging, and strict temperature control (−1.5±0.5°C) can enhance storage life and, therefore, distribution ease. An insulated shipping and storage container was designed and tested for its suitability to distribute master-packaged meat. Shelves in the container supported 36 master trays (508 × 381 × 60 mm), with the source of refrigeration being injected liquid nitrogen (N₂). Electric fans dispersed the N₂ gas throughout the container. To reduce costs, 36 saline water bags (10% w/v NaCl) were used to thermally simulate the meat. Temperatures of 20 bags were recorded during storage experiments. The container was tested at outside temperatures of 15, 0 and −15°C with 4 internal fans and at 30°C with 2, 4 and 6 fans. In all instances, bags cooled from 10°C to an equilibrium temperature of −1.5°C within 5.5 h. Minimum equilibrium temperatures during any 8 h trial were −2.6, −2.0 and −2.0°C for 2, 4 and 6 fans, respectively. Correspondingly, maximum temperatures were −0.2, −0.7 and −0.3°C. Initial chilling of the product required, on average, 19 kg of N₂, while equilibrium was maintained at a N₂ consumption rate of 5.5, 4.0, 2.6 and 0.93 kg/h at outside temperatures of 30, 15 0 and −15°C, respectively, with 4 fans. The N₂ use for 2 and 6 fans was 5 and 6.3 kg/h, respectively, at an outside temperature of 30°C. During simulated power failure or when the N₂-tank ‘ran dry', temperatures in the container rose 0.9 and 2.0°C/h, respectively. When the door to the container was opened long enough to remove three trays, temperature was restored within 5 min. Convective heat transfer coefficients between saline water bags and circulating N₂ were in the range of 80–100, 115–135, and 140–155 W/(m²·K) for 2, 4 and 6 fans, respectively. Heat transfer to meat will be limited by conduction in master packaged meat if similar convection coefficients prevail.     

Conventional freezing plus high pressure-low temperature treatment: Physical properties, microbial quality and storage stability of beef meat

Meat high-hydrostatic pressure treatment causes severe decolouration, preventing its commercialisation due to consumer rejection. Novel procedures involving product freezing plus low-temperature pressure processing are here investigated. Room temperature (20 °C) pressurisation (650 MPa/10 min) and air blast freezing (−30 °C) are compared to air blast freezing plus high pressure at subzero temperature (−35 °C) in terms of drip loss, expressible moisture, shear force, colour, microbial quality and storage stability of fresh and salt-added beef samples (Longissimus dorsi muscle). The latter treatment induced solid water transitions among ice phases. Fresh beef high pressure treatment (650 MPa/20 °C/10 min) increased significantly expressible moisture while it decreased in pressurised (650 MPa/−35 °C/10 min) frozen beef. Salt addition reduced high pressure-induced water loss. Treatments studied did not change fresh or salt-added samples shear force. Frozen beef pressurised at low temperature showed L, a and b values after thawing close to fresh samples. However, these samples in frozen state, presented chromatic parameters similar to unfrozen beef pressurised at room temperature. Apparently, freezing protects meat against pressure colour deterioration, fresh colour being recovered after thawing. High pressure processing (20 °C or −35 °C) was very effective reducing aerobic total (2-log₁₀ cycles) and lactic acid bacteria counts (2.4-log₁₀ cycles), in fresh and salt-added samples. Frozen + pressurised beef stored at −18 °C during 45 days recovered its original colour after thawing, similarly to just-treated samples while their counts remain below detection limits during storage.     

Combined effect of modified atmosphere bulk packaging, dietary vitamin E supplementation and microbiological contamination on colour stability of Musculus gluteus medius

Five Simmentaler type calves were fed diets supplemented with 500 mg vitamin E per day and five fed control diets. Rump steaks from each carcass were PVC-overwrapped and bulk packaged in 100% CO, or 20% CO₂:80% O₂. Bulk packs were stored up to 42 days at 4°C and steaks displayed up to 7 days at 4°C. Bacterial counts of rump steaks from either packaging treatment were not significantly influenced during bulk storage or retail display by supplementation with dietary vitamin E. Both packaging treatments delayed bacterial growth during bulk storage. Aerobic plate counts of rump steaks stored in 100% CO₂ were lower than those of rump steaks stored in 20% CO₂: 80%: O₂. This study showed that rump steaks supplemented with dietary vitamin E can be bulk packaged in 20% CO₂: 80% O₂ or 100% CO₂ and stored for up to 42 days with shelf life of 4–7 days.     

Influence of various preservatives on the quality of minced beef under modified atmosphere at chilled storage

The effect of preservatives on microbial quality, pH, drip-loss, roasting-loss, colour, and sensorial properties of modified atmosphere packaged (70% O₂ and 30% CO₂) minced beef (M. semimembranosus) stored at (2 ± 0.5 °C) for 12 days was investigated. Beef cubes (approx. 20 × 20 × 20 mm size) were immersed in solutions of 2% and 5% lactic acid, 2% lactic acid combined with 0.5% sodium ascorbate, 20% potassium lactate and 20% potassium sorbate before mincing. Addition of lactic acid was associated with pH drop, which increased drip-loss and roasting-loss. Application of all additives inhibited aerobic micro-organisms (10³–10⁴ CFU g⁻¹ on day 12) compared to reference sample (9 × 10⁵ CFU g⁻¹ on day 12). Lactic acid discoloured samples, while sodium ascorbate seemed to improve colour stability. Despite good visual colour characteristics, potassium sorbate treated samples were organoleptically unacceptable with massive off-flavour.     

Effect of modified atmospheres on microbiological, color and sensory properties of refrigerated pork

Pork loin samples were stored (4 °C) in nylon polyethylene plastic bags using different modified atmospheres packaging (MAP): vacuum, 100% CO₂ 99% CO₂ + 1% CO, 100% O₂ or 100% CO followed by vacuum. Throughout the storage period Pseudomonas growth was limited in loins packaged in all MAPs evaluated, except for 100% O₂. Psychrotrophs reached 10⁷ CFU g⁻¹ after 20 days of storage except for the loin samples in 100% O₂ MAP that present count above 10⁸ CFU g⁻¹. The 1% CO/99% CO₂ atmosphere was best for preserving the desirable pork loin color and the L* and a* values remained similar to the fresh meat values using this MAP. Pork loins in 99% CO₂/1% CO MAP obtained the highest consumer acceptance scores after 24 h of storage. These samples and those treated with CO and then vacuum packaged received the greatest acceptance scores even after 20 days of storage.     

The effect of wholesale vacuum and 100% CO2 storage on the subsequent microbiological, colour and acceptability attributes of PVC-overwrapped pork loin chops

The shelf life of chops cut from pork loins, after either vacuum or 100% CO₂ storage (0, 7 or 14 days), was determined. The PVC-overwrapped chops were assessed, following a shelf life study of 0, 2, 5 or 7 days at 0 or 5°C, regarding quality attributes such as microbiological contamination levels, colour and acceptability. The study indicated that according to the psychrotrophic counts, the PVC-overwrapped retail chops, from the vacuum as well as the 100% CO₂ stored pork loins (0, 7 or 14 days), still attained a conventional shelf life of 3 days.

Lactic acid bacteria and pseudomonads largely represented the psychrotrophic counts. No clear pattern could be detected regarding the colour scores except that the samples displayed at 0°C tended to retain colour longer. These samples were also judged to be more acceptable, although the determination of acceptability was subjective.     

Addition of grape seed extract and bearberry to porcine diets: Influence on quality attributes of raw and cooked pork

The effect of supplementation of pig diets with grape seed extract (GSE) (100, 300, 700 mg/kg feed) and bearberry (BB) (100, 300, 700 mg/kg feed) for 56 days pre-slaughter, on the oxidative stability and quality of raw and cooked M. longissimus dorsi (LD) was examined. Susceptibility of porcine liver, kidney and heart tissue homogenates to iron-induced (1 mM FeSO₄) lipid oxidation was also investigated. In raw LD steaks, stored in modified atmosphere packs (75% O₂:25% CO₂) (MAP) for up to 16 days at 4 °C, surface lightness (CIE ‘L’ value), redness (CIE ‘a’ value), lipid stability (TBARS, mg MDA (malondialdehyde)/kg muscle) and pH were not significantly affected by supplemental GSE or BB. Similarly, the oxidative stability and sensory properties of cooked LD steaks, stored in MAP (70% N₂:30% CO₂), for up to 28 days at 4 °C, were not enhanced by dietary GSE or BB. Iron-induced lipid oxidation increased in liver, kidney and heart tissue homogenates over the 24 h storage period and susceptibility to oxidation followed the order: liver > heart > kidney. Dietary GSE or BB did not significantly reduce lipid oxidation in tissue homogenates. Potential reasons for the lack of efficacy of supplemental GSE and BB on pork quality were explored.     

The effects of spray and blast-chilling on carcass shrinkage and pork muscle quality

Combinations of blast- and spray-chilling of pork carcasses were compared to spray-chilling at conventional chilling temperatures with regard to carcass shrinkage during chilling and pork muscle quality. In experiment 1, pork sides were spray-chilled at 1°C for the first 10 h (40 spray cycles of 60-s duration every 15 min) of cooling or blast-chilled at −20°C for 1, 2 or 3 h followed by spray-chilling for 9, 8 or 7 h duration, respectively. All pork sides were then chilled to 24 h post mortem at 1°C. Experiment 2 followed the same procedures as experiment 1, except that −40°C was used as the blast-chill temperature.

Carcass shrinkage was similar for all treatments in experiment 1 at 24 h ranging from 0·5–0·7 g 100 g⁻¹. Blast/spray-chilling increased the rate of chilling and reduced the rate of post-mortem pH decline in two muscles (longissimus thoracis, LT and semimembranosus, SM) compared to the combined conventional/spray-chill treatment. Carcasses that were blast-chilled for 3 h had LT muscles that were darker with a higher protein solubility, less drip loss, shorter lengths and higher shear values compared to those from carcasses in the conventional/spray-chill treatment. In experiment 2, carcasses blast-chilled for 3 h at −40°C recorded a weight gain at 24 h of 0·4 g 100 g⁻¹, compared to a weight loss in all other treatments (0·2–0·4 g 100 g⁻¹). Muscle colour was darker in both the LT and SM of carcasses blast-chilled for 3 h at −40°C compared to carcasses from the conventional/spray-chill treatment, but most other measurements of muscle quality showed an inconsistent response to chilling treatment.     

Effect of dietary supplementation of vitamin E on characteristics of lamb meat packed under modified atmosphere

The effect of dietary vitamin E supplementation on modified-atmosphere packed lamb meat during storage was studied. Thirty-six weaned male Manchego breed lambs were fed diets supplemented with three different vitamin E concentrations (0, 250, 500 and 1000 mg/kg feed) for an average of 37 days, in the 13–26 kg live weight growth range. Slices of m. longissimus dorsi were packaged under modified atmosphere (70% O₂ and 30% CO₂), stored at 2 ± 1 °C in darkness for 14 and 28 days. Meat quality parameters after both storage periods were assessed. Dietary vitamin E supplementation significantly increased -tocopherol concentration in muscle. Initially, lipid oxidation (TBARS), meat colour and bacterial load were similar in all groups. Lipid and colour oxidation of meat increased significantly (P < 0.001) throughout storage. The increase was greater in non-supplemented lambs than in supplemented ones. The bacterial counts after 28 days of storage reached the limit for microbiological shelf life (7 log₁₀cfu/cm²). Dietary vitamin E supplementation increased the shelf life of meat packaged under modified atmosphere to 14 days. TBARS, pigment oxidation and bacterial load were inside the acceptable limit. The meat maintained its quality for 28 days of storage only when lambs were fed with the 1000 mg/kg dietary supplement, though the bacterial load was at the limit of acceptability.     

Evaluation of the antioxidant potential of grape seed and bearberry extracts in raw and cooked pork

The effect of grape seed extract (GSE) and bearberry (BB), on lipid oxidation (TBARS, mg malondialdehyde (MDA)/kg muscle), colour (CIE ‘a’ redness value), pH, microbial status (log₁₀CFU colony forming units/g pork) and sensorial properties of cooked pork patties was investigated. GSE (0–1000 μg/g muscle) and BB (0–1000 μg/g muscle) were added to raw pork (M. longissimus dorsi) patties which were stored in modified atmosphere packs (MAP) (75% O₂:25% CO₂) for up to 12 days at 4 °C. Cooked pork patties were stored in MAP (70% N₂:30% CO₂) for up to 4 days at 4 °C. Mesophilic plate counts and pork pH were unaffected by GSE and BB. GSE and BB addition decreased (P < 0.05) lipid oxidation (TBARS) in raw pork patties on days 9 and 12 of storage, relative to controls. Antioxidant activity of GSE and BB was observed in cooked pork patties demonstrating the thermal stability of GSE and BB. The ‘a’ redness values of raw and cooked pork patties marginally increased with increasing GSE concentration. The sensory properties of cooked pork patties were unaffected by GSE and BB addition. Results obtained demonstrate the potential for using health promoting nutraceuticals in meat and meat products.     

Diffusion of thiocyanate and hypothiocyanite in whey protein films incorporating the lactoperoxidase system

The diffusion of the thiocyanate (SCN⁻) and hypothiocyanite (OSCN⁻) components of a lactoperoxidase system (LPOS) in whey protein isolate (WPI) films was investigated. Diffusion coefficients for these molecules were measured for the LPOS-incorporated WPI films prepared with different WPI:glycerol ratios (1:1, 3:1, and 5:1). WPI film disks were coated on the surfaces of smoked salmon samples, and the samples were stored at 4, 10 and 22 °C. The diffusion coefficients were determined by fitting a mathematical model to the amounts of SCN⁻ and OSCN⁻ released from the disks during a period of time. The diffusion coefficients for SCN⁻ (D₁) and OSCN⁻ (D₂) in the films were 0.19–5.2 × 10⁻¹² m² s⁻¹ and 0.13–6.5 × 10⁻¹³ m² s⁻¹, respectively. The D₁ and D₂ decreased as the WPI:glycerol ratio increased and the storage temperature decreased. The E_a values for diffusion in 1:1, 3:1, and 5:1 WPI:glycerol films were 13.3, 29.5, and 35.6 kJmol⁻¹, respectively, for SCN⁻ and 15.8, 30.1, and 39.9 kJmol⁻¹, respectively, for OSCN⁻.     

Centralised bulk pre-packaging of fresh pork retail cuts in various gas atmospheres

A centralised bulk pre-packaging technique (laboratory method), utilising various gas mixtures (c. 100% CO₂; c. 75% CO₂:25% N₂; c. 80% O₂: 20% CO₂ and c. 25% CO₂:50% N₂:25% O₂), was evaluated in terms of quality attributes such as microbiology, colour, odour and consumer acceptability. According to the bacterial counts recorded, all four packaging treatments were successful in prolonging the storage life (21 days c. 0°C) of centralised bulk pre-packaged pork retail cuts, while still ensuring a subsequent shelf life of at least 3 days (c. 0°C). The gas mixture comprising c. 25% CO₂:50% N₂:25% O₂ was the most successful treatment in terms of acceptability and colour scores.     

A novel use of modified atmospheres: Storage insect population control

The research described here aimed to establish the feasibility of using modified atmospheres (MA) to protect commodities throughout their storage life by using oxygen (O₂) levels that disrupt the life cycles of the target beetle species. Rather than achieving complete mortality of all stages, the aim was to identify more easily obtainable MAs that would kill the most susceptible stage and prevent population growth. Simulated burner gas and nitrogen (N₂) atmospheres with O₂ contents between 3% and 6%, were tested, along with a N₂-based MA with elevated carbon dioxide (CO₂) (10–20%).

Laboratory tests were carried out on five species of stored-product beetles, Cryptolestes ferrugineus, Oryzaephilus surinamensis, Sitophilus granarius, S. oryzae and Tribolium castaneum. After exposure to the MAs for 28 d an assessment was made of the mortality of adults, the number of adults from progeny produced under the MAs and, for the simulated burner gas, the number of adults from progeny produced in a 28-d period after exposure to the MA. The tests were carried out at 20 and 25 °C with 75% and 85% r.h. at each temperature.

The O₂ content preventing population growth varied with species and temperature. For simulated burner gas or N₂ it was about 4% for O. surinamensis, S. granarius and S. oryzae, and about 3% for C. ferrugineus and T. castaneum at 25 °C. At 20 °C it was about 3% for all species tested. When CO₂ was increased to 10% or 20%, reducing O₂ to 5% was sufficient to eliminate emergence of S. granarius at 20°C, but a few individuals emerged at 25 °C. For C. ferrugineus there was a 95% reduction with 5% O₂ plus 20% CO₂ at 20 °C, but not at 25 °C.     

Beef shelf life in low O(2) and high CO(2) atmospheres containing different low CO concentrations

The use of atmospheres with low concentrations of CO (0.1 to 1%), in combination with O₂ (24%), high CO₂ (50%) and N₂ (25 to 25.9%), for preserving chilled beef steaks was investigated. The atmosphere used as reference contained 70% O₂+20% CO₂+10% N₂. Bacterial counts showed that all atmospheres containing CO greatly reduced total aerobic population numbers, including Brochothrix thermosphacta. Lactic acid bacteria, however, were not affected. CO concentrations of 0.5–0.75% were able to extend shelf life by 5–10 days at 1±1°C, as demonstrated by delayed metmyoglobin formation (less than 40% of total myoglobin after 29 days of storage), stabilisation of red colour (no change of CIE a* and hue angle after 23 days), maintenance of fresh meat odour (no variation of sensory score after 24 days) and significant (P<0.01) slowing of oxidative reactions (TBARS).     

Frozen storage conditions and rancid flavour development in lamb

Frozen storage of lamb at temperatures of −5 or −10°C before ultimate storage at −35°C induced changes that led to rancidity development (as assessed by a taste panel) continuing at a more rapid rate at the lower temperature. Parallel storage regimes, but with storage at −35°C first, then ultimate storage at −5°C or −10°C, led to much less storage flavour development.

No significant flavour changes occurred even after 40 weeks storage at −15°C followed by 20 weeks storage at −35°C.

These studies emphasise the importance of order of time-temperature holding treatments in studies of rancid flavour development and indicate that time-temperature effects may not be truly additive.