UV-C treatment delays postharvest senescence in broccoli florets

Central broccoli heads (cv. de Cicco) were harvested and treated with UV-C light (4, 7, 10, or 14 kJ m⁻²). All treatments delayed yellowing and chlorophyll degradation at 20 °C but the irradiation dose of 10 kJ m⁻² allowed retaining the highest chlorophyll content yet had lower amounts of pheophytins than every treatment other than 7 kJ m⁻². This dose was selected to analyze the effect of UV-C on postharvest broccoli senescence at 20 °C. The UV-C treatment delayed yellowing, chlorophyll a and b degradation, and also the increase in pheophytins during storage. The activity of chlorophyll peroxidase and chlorophyllase was lower in UV-C treated broccoli. Instead, Mg-dechelatase activity increased immediately after the treatment, but after 4 and 6 d this activity was lower in UV-C treated florets than in controls. Treated broccoli also displayed lower respiration rate, total phenols and flavonoids, along with higher antioxidant capacity. The results suggest that UV-C treatments could be a useful non-chemical method to delay chlorophyll degradation, reduce tissue damage and disruption, and maintain antioxidant capacity in broccoli.     

Postharvest UV-C irradiation on cut Freesia hybrida L. inflorescences suppresses petal specking caused by Botrytis cinerea

Postharvest petal specking caused by Botrytis cinerea is a major concern for freesia growers and sellers in Holland and the UK. Germicidal and inducible host defence effects of UV-C irradiation were evaluated. UV-C irradiation of freesia inflorescences after artificial inoculation with B. cinerea (i.e. the germicidal effect) was more effective in reducing petal specking, compared to UV-C treatment before artificial inoculation (i.e. the defence induction effect). Cut freesia inflorescences exposed to 1 kJ m^?2 UV-C after artificial inoculation with 10⁴ B. cinerea conidia mL^?1 displayed reduced disease severity scores, lesion numbers and lesion diameters by 74, 68 and 14%, respectively, compared to non-irradiated control inflorescences. In contrast, UV-C irradiation with 1 kJ m^?2 before artificial inoculation reduced lesion numbers and lesion diameters by 13 and 24%, compared to the non-irradiated controls. Higher UV-C doses of 2.5 or 5 kJ m^?2 reduced disease severity scores, lesion numbers and lesion diameters when applied after artificial inoculation, but enhanced disease when applied before artificial inoculation. Vase life of cut freesia inflorescences irradiated with 0.5, 1 or 2.5 kJ m^?2 UV-C was maintained equal to non-irradiated controls. However, 5 kJ m^?2 resulted in phytotoxicity evident as petal discoloration and reduced vase life compared to non-irradiated inflorescences.     

Controlling sprouting in potato tubers using ultraviolet-C irradiance

Legislation limiting the use of chlorpropham (CIPC), the major potato sprout suppressant, has led to a need for new technologies to extend storage life of tubers. Ultra violet C (UV-C) has been used postharvest to reduce disease incidence on many crops, yet its use and efficacy as a sprout suppressant has not been investigated. The aim of this project was to identify the optimum dose and treatment timing of UV-C treatment on potato tubers as an alternative method of sprout suppression to reduce the dependence on chemical sprout suppressants. Up to six potato cultivars over two seasons were treated with varying doses of UV-C ranging from 0 to 30 kJ m⁻² either at harvest or at first indication of dormancy break. The tubers were stored at 9 °C and sprout growth and incidence assessed. Treatment with moderate UV-C doses (5–20 kJ m⁻²) suppressed sprout length and sprout incidence in a range of cultivars. Periderm DNA damage and programmed cell death were not detected in response to any of the UV-C doses. The inactive ABA metabolite, ABA-GE, increased in response to 10 or 20 kJ m⁻² within 72 h of treatment. Multivariate analysis showed a negative relationship between ABA metabolites and sprout growth/incidence during storage. This study found that UV-C reduced sprout growth in potato with no deleterious effects on tuber quality. This suggests potential for further development as an alternative or supplement to conventional sprout suppressant technologies.     

UV-C light inactivation kinetics of Penicillium expansum on pear surfaces: Influence on physicochemical and sensory quality during storage

UV-C inactivation kinetic data of Penicillium expansum on intact and wounded pear disks were determined. P. expansum conidia (0.5 mL, 1.6 × 10⁷ CFU/mL) were spot inoculated onto intact and wounded pear tissue with skin (excised disks), treated with UV-C doses ranging 0.101–3.06 kJ/m² at 23 °C and surviving conidia were enumerated. Changes in selected physicochemical parameters and sensory quality following UV-C treatment of whole pears were determined immediately after treatment, and 4 and 8 weeks of storage at 4 °C. A greater UV-C intensity was required for similar inactivation levels of P. expansum populations on wounded pear disks (3.1 kJ/m² for 2.7 log reduction) compared to intact pear disks (1.7 kJ/m² for 2.8 log reduction). No significant difference in % weight loss, or soluble solids content and texture was observed between UV-C treated and untreated pears. However, browning was observed on UV-C treated pear surfaces after 4 and 8 weeks along with changes in flavor and texture. An increase in consumer preference was noticed for the untreated control pears after 4 weeks storage.     

Flesh quality and lycopene stability of fresh-cut watermelon

Red fleshed watermelons are an excellent source of the phytochemical lycopene. However, little is known about the stability of lycopene in cut watermelon. In this study, lycopene stability and other quality factors were evaluated in fresh-cut watermelon. Twenty melons each of a seeded (Summer Flavor 800) and a seedless (Sugar Shack) variety were cut into 5 cm cubes and placed in unvented polystyrene containers, sealed, and stored at 2 °C for 2, 7, or 10 days. At each storage interval, melons were evaluated for juice leakage, changes in carotenoid composition, color, soluble solids content (SSC), and titratable acidity. Headspace carbon dioxide and ethylene were monitored during storage intervals. Juice leakage after 10 days of storage averaged 13 and 11% for the seeded and seedless melons, respectively. Lycopene content decreased 6 and 11% after 7 days of storage for Summer Flavor 800 and Sugar Shack melons, respectively. β-Carotene and cis lycopene contents were 2 and 6 mg kg⁻¹ for Summer Flavor 800 and Sugar Shack, respectively, and did not change with storage. After 10 days of storage, CIE L¹ values increased while chroma values decreased, indicating a lightening in color and loss of color saturation in melon pieces. Symptoms of chilling injury, such as greatly increased juice leakage, or lesions on cubes, were not seen on the fresh-cut cut watermelon after 10 days storage at 2 °C. Puree pH increased and SSC decreased slightly after storage. Carbon dioxide levels increased and oxygen levels decreased linearly during storage, creating a modified atmosphere of 10 kPa each of CO₂ and O₂ after 10 days. Fresh-cut cut watermelon held for 7 or more days at 2 °C had a slight loss of SSC, color saturation, and lycopene, most likely caused by senescence.     

UV-B irradiation retards chlorophyll degradation in lime (Citrus latifolia Tan.) fruit

Peel yellowing is a major postharvest problem of lime fruit. Research was conducted to control peel yellowing by UV-B irradiation. Mature green lime fruit were irradiated with UV-B doses at 0 (control), 8.8, and 13.2 kJ m^?2 and then stored at 25 °C in darkness. UV-B treatment at 8.8 kJ m^?2 efficiently delayed the decrease of chlorophyll content. A high level of chlorophyllide a accumulated in mature green fruit and then gradually decreased with the progress of peel yellowing. The chlorophyllide a level was higher in 8.8 kJ m^?2 UV-B-treated fruit than it was in the controls. The pheophorbide a level declined in lime fruit treated with 8.8 kJ m^?2 UV-B, especially during the development of yellowing. In addition, the pheophytin a level increased by 8.8 kJ m^?2 UV-B treatment at the late period of storage. We concluded that UV-B treatment effectively suppressed chlorophyll degradation in mature green lime during storage, which suggests that UV-B irradiation is a usable method for prolonging the postharvest life of lime fruit.     

Effects of gamma and UV-C irradiation on the postharvest control of papaya anthracnose

Anthracnose is the main postharvest disease in papaya fruit. Today, there is considerable interest on alternative methods of control to promote resistance against pathogens and supplement or replace the use of fungicides. The goal of this work was to evaluate the effects of gamma and UV-C irradiation on Colletotrichum gloeosporioides, the causal agent of anthracnose. Mycelial growth, sporulation, and conidial germination were evaluated in vitro after fungal exposition to different irradiation doses. In the in vivo assays, ‘Golden’ papaya fruit were inoculated through subcuticular injections of a conidial suspension or mycelium discs. Next, fruit were submitted to different irradiation doses (0, 0.12, 0.25, 0.5, 0.75, and 1 kGy), using Co⁶⁰ as source, or UV-C (0, 0.2, 0.4, 0.84, 1.3, and 2.4 kJ m⁻²). To check the possibility of resistance induction by irradiation, papayas were also inoculated 24, 48, or 72 h after the treatments. The fruit were stored at 25 °C/80% RH for 7 days and evaluated for incidence and rot severity. The results showed that the 0.75 and 1 kGy doses inhibited conidial germination and mycelial growth in vitro. All doses increased fungal sporulation. The 0.75 and 1 kGy doses reduced anthracnose incidence and severity, but did not reduce them when the fruit were inoculated after irradiation. All UV-C doses inhibited conidial germination and those higher than 0.84 kJ m⁻² inhibited mycelial growth. The 0.4, 0.84, and 1.3 kJ m⁻² UV-C doses reduced fungal sporulation in vitro. There was no effect of UV-C doses and time intervals between treatment and inoculation on anthracnose control and fungal sporulation in fruit lesions. Moreover, all UV-C doses caused scald on the fruit. Thus, gamma irradiation can contribute for the reduction of postharvest losses caused by anthracnose and reduce the use or doses of fungicides on disease control.     

Effect of UV-C treatments on phenolic compounds and antioxidant capacity of minimally processed Satsuma mandarin during refrigerated storage

The effect of UV-C treatments (0.75, 1.5 and 3.0 kJ/m²) on fruit quality, phenolic compounds and antioxidant capacity of minimally processed Satsuma mandarin during 12 days of storage at 4 °C was studied. The results showed that UV-C treatments had no adverse effects on quality attributes, ascorbic acid, phenolic acids and antioxidant capacity of mandarin segments. Significant increases of flavonoids (22.20% and 21.34% for narirutin, 11.75% and 33.25% for hesperidin) and total phenolics (5.73% and 8.13%) were found in 1.5 and 3.0 kJ/m² UV-C treated fruit at 3 days of storage. Further study confirmed that the increase of flavonoids occurred during the first 3 days and diminished after 4 days of storage. UV-C dose at 3.0 kJ/m² did not further improve the increase of flavonoids, and 0.75 kJ/m² had no significant effects on phenolics. Proper application of UV-C treatment could be a new way to enhance the functional quality of minimally processed citrus fruit.     

The combined effects of aqueous chlorine dioxide,fumaric acid,and ultraviolet-C with modified atmosphere packaging enriched in CO2 for inactivating preexisting microorganisms and Escherichia coli O157:H7 and Salmonella typhimurium inoculated on buckwheat sprouts

The combined effects of a sanitizer mixture, ultraviolet-C (UV-C), and modified atmosphere packaging (MAP) on the quality of non-inoculated and inoculated (Escherichia coli O157:H7 and Salmonella typhimurium) buckwheat sprouts were examined. Buckwheat sprouts were treated with a sanitizer mixture (comprising 100 mg L⁻¹ aqueous ClO₂ and 0.3% fumaric acid) and 2 kJ m⁻² UV-C, packaged under two different conditions (air and CO₂ gas) and storage for 8 d at 4 °C. The combination of the sanitizer mixture and UV-C treatment reduced the initial counts of preexisting microorganisms in the buckwheat sprouts by 1.9 log CFU g⁻¹ and reduced the initial inoculated counts of E. coli O157:H7 and S. typhimurium on buckwheat sprouts by 3.0 and 2.3 log CFU g⁻¹, respectively. The preexisting microorganisms and inoculated pathogens in buckwheat sprouts packaged under CO₂ gas were significantly reduced during storage following the combined treatment compared to those of the control by above 95%. Differences in Hunter L^*, a^*, and b^* values among the treatments were negligible. The combined sanitizer mixture and UV-C treatment increased the sprout rutin content by 147%, but there was no significant difference in 2,2-diphenyl-1-picrylhydrazyl radical scavenging activity between treatments during storage. Therefore, the combination of sanitizer mixture made from aqueous ClO₂ and fumaric acid, UV-C irradiation, and MAP can improve the microbial safety and quality of buckwheat sprouts.     

UV-C inactivation of Escherichia coli and dose uniformity on apricot fruit in a commercial setting

A UV-C treatment system (two treatment chambers connected by an inclined belt to rotate apricots between chambers) was tested in a commercial setting. Escherichia coli ATCC 25922, used as a surrogate for E. coli O157:H7 to determine the system's antimicrobial efficacy, was inoculated onto fruit surfaces at a population of 6.8 log CFU/fruit. UV-C dosage was evaluated by attaching film dosimeters to six fixed locations on each apricot. Results suggested that reduction of inoculated E. coli ATCC 25922 populations on the apricot fruit by UV-C treatment was small (only 0.5–0.7 logs). There were large variations in UV-C doses among varying apricot surface locations. Approximately 1/3 of apricots had individual surfaces receiving less than 0.2 kJ m⁻² UV-C exposure, even though fruit received, on average, more than 1 kJ m⁻². Low reductions of E. coli may be attributed, in part, to non-uniform UV-C exposure. This study demonstrates the need to use a fruit rotation device more capable of delivering uniform UV-C dosage to the surface of apricots for inactivating bacteria in a commercial setting.     

Low dose UV-C illumination as an eco-innovative disinfection system on minimally processed apples

In this study, the efficacy of UV-C illumination for inactivate Escherichia coli, Listeria innocua or Salmonella enterica, individually or in a mixture, in vitro and on apple slices was determined. Apple slices inoculated with a 10⁷ cfu/mL suspension of above indicated pathogens were irradiated on both sides with UV-C illumination, with doses of 0.5 and 1.0 kJ/m². UV-C illumination disinfection efficacy was compared to that of washings with sodium hypochlorite at 100 ppm of free chlorine and with distilled water. Bactericidal activity of each treatment was assessed after 30 min and after 7 and 15 days of storage at 4 °C. Results showed that UV-C illumination at 1.0 kJ/m² could be an alternative to the wash with hypochlorite solutions. On the in vitro study, these doses completely inhibited the growth of the three bacteria either as pure cultures or in a mixture. In fresh-cut apple, the pathogens were also affected by the UV-C illumination, the 1.0 kJ/m² dosage being the one that resulted in higher bacteria inhibition in almost every case. The UV-C treatment did not affect the quality properties of fresh-cut apple.     

Postharvest ultraviolet-C irradiation suppressed Psy 1 and Lcy-β expression and altered color phenotype in tomato (Solanum lycopersicum) fruit

Mature green cherry tomato fruit were harvested and treated with ultraviolet-C (UV-C) irradiation at a predetermined dose of 4.2 kJ m⁻², and stored at 18 °C for 35 days. The effects of UV-C treatment on color change, pigment contents, and the expression of major genes involved in carotenoid metabolism, including Psy 1, Pds, Lcy-β, and Lcy-ɛ, encoding phytoene synthase, phytoene desaturase, lycopene β-cyclase and lycopene ɛ-cyclase, respectively, were examined. The UV-C treated fruit developed a pink red color in contrast to the normal orange red color of control fruit. Lycopene accumulation during ripening in UV-C treated fruit was significantly inhibited but its final content was not affected. However, both accumulation and final content of β-carotene were significantly suppressed in UV-C treated fruit. The lower content of β-carotene, leading to a higher lycopene to β-carotene ratio, is probably responsible for the altered color phenotype in UV-C treated fruit. Psy 1, a major gene involved in lycopene synthesis was inhibited by UV-C irradiation. Significantly suppressed expression of Lcy-β gene was also observed in UV-C treated fruit. Thus it is possible that the lower transformation from lycopene to carotenes contributed to the relatively stable content of lycopene.     

Influence of UV-C treatment on antioxidant capacity,antioxidant enzyme activity and texture of postharvest shiitake (Lentinus edodes) mushrooms during storage

Shiitake (Lentinus edodes) mushrooms were exposed to UV-C light (4 kJ/m²) and stored in modified atmosphere packaging (MAP) prior to 15 days at 1 ± 1 °C and 95% relative humidity plus 3 days at 20 °C. Mushroom firmness, total phenolics, total flavonoids, ascorbic acid and H₂O₂ contents, superoxide anion (O₂⁻) production rate and activities of catalase (CAT), superoxide dismutase (SOD), ascorbate peroxidase (APX) and glutathione reductase (GR) were measured. UV-C treatment resulted in maintenance of a high level of firmness during 15 days at low temperature and reduced the decrease in firmness during shelf-life storage. Furthermore, treated samples showed higher total flavonoids, ascorbic acid, and delayed the increases in both O₂⁻ production rate and H₂O₂ contents. However, no clear treatment effects were seen in total phenolics contents. The treatment also increased the antioxidant enzyme activities of CAT, SOD, APX and GR throughout the storage period. These results indicate that postharvest application of UV-C radiation can delay softening and enhance antioxidant capacity in shiitake mushrooms.     

Vitamin C in broccoli (Brassica oleracea L. var. italica) flower buds as affected by postharvest light,UV-B irradiation and temperature

In this study, the changes in vitamin C, l-ascorbic acid (AA) and l-dehydroascorbic acid (DHA) levels in broccoli flower buds were examined during pre-storage and storage periods, simulating refrigerated transport with wholesale distribution and retail, respectively. Broccoli heads were pre-stored for 4 or 7 days at 0 °C or 4 °C in the dark and then stored for 3 days at 10 °C or 18 °C. During storage the broccoli heads were exposed for 12 h per day to three different levels of visible light (13, 19 or 25 μmol m⁻² s⁻¹) or a combination of visible light (19 μmol m⁻² s⁻¹) and UV-B irradiation (20 kJ m⁻² d⁻¹), or they were stored in the dark. The vitamin C content in broccoli flower buds during storage was significantly affected by pre-storage period and temperature. Higher vitamin C levels in flower buds after storage were observed for broccoli heads pre-stored for 4 days or at 0 °C as compared to those pre-stored for 7 days or at 4 °C. Storage temperature also affected vitamin C in broccoli flower buds, with higher levels observed for broccoli stored at 10 °C than at 18 °C. Hence, vitamin C in broccoli flower buds was demonstrated to decrease together with increasing pre-storage period, pre-storage temperature and storage temperature. AA in broccoli flower buds was influenced mainly by storage temperature and to a minor extent by pre-storage temperature. The DHA level and DHA/AA ratio were stable in flower buds of broccoli pre-stored for 7 days, whereas increasing tendencies for both DHA level and ratio were observed after pre-storage for 4 days. These results indicate a shift in the ascorbate metabolism in broccoli flower buds during storage at low temperatures, with its higher rate observed for broccoli pre-stored for shorter time. There were no effects of the light and UV-B irradiation treatments on vitamin C, AA and DHA levels in broccoli flower buds.     

Conventional and emergent sanitizers decreased Ectomyelois ceratoniae infestation and maintained quality of date palm after shelf-life

Several methods have been used to prevent pest diseases and microbial contamination of dates, although their use is being restricted due to harmful effects on humans and/or to the environment. Sustainable sanitation techniques for keeping overall quality and safety of harvested dates should be developed and implemented. The current work studied the effect of NaClO, UV-C, ozonated water and alkaline and neutral electrolyzed water (NEW) on natural infestation by Ectomyelois ceratoniae or moth of pyrale, and on overall quality of ‘Deglet Nour’ dates stored for 30 days at the commercially used temperature of 20 °C. As controls, untreated samples were used. The skin color, firmness, pH, titratable acidity, total soluble solids content, sugar content, total polyphenols, antioxidant activity, microbial counts, sensory quality and moth infestations were monitored. Phenolics content increased after shelf-life. As expected, all sanitizers lowered microbial counts and moth infestation. A dose of 6 kJ UV-C m⁻² was the most efficient treatment against yeast and molds (without differences with NaClO and O₃), and coliforms, maintaining overall quality of dates after shelf-life. UV-C and NEW (pH 7.2, ORP 814 mV, and 300 mg L⁻¹ of free chlorine) were the most effective against moth proliferation, and could be considered as promising useful tools for commercial disinfection of fresh dates and extending shelf-life. As far as we know, no other comparative studies on these postharvest sanitizers on dates have been reported.     

Effect of radiation intensity on the outcome of postharvest UV-C treatments

Studies on the use of UV-C radiation of fresh produce have focused on the selection of appropriate doses (energy per unit area) for different commodities, but little attention has been placed on the effect of radiation intensity (dose per unit time). In this study, tomatoes (Solanum lycopersicum cv. Elpida) and strawberries (Fragaria × ananassa cv. Camarosa), were harvested (breaker and 100% of surface red color respectively) and treated with 4 kJ m⁻² of UV-C, at low (3 W m⁻²) or high (33 W m⁻²) radiation intensities. Untreated fruits were used as controls. After the treatments and at different storage times the incidence of postharvest rots and the changes in fruit physical and chemical properties were determined. UV-C treatments reduced decay, with the effects being were more marked in fruit exposed to high intensities. Mold counts were unaffected by the treatments, suggesting that improved disease control did not result from greater germicide effect. In both fruit species exposure to UV-C radiation delayed ripening, evidenced as lower color development, pigment accumulation and softening. UV-C-treated fruit maintained better quality than the control. In strawberry, high intensity treatments were more effective to prevent deterioration than in tomato where the differences between UV-C treatments were subtler. Soluble solids, titratable acidity and ethanol soluble antioxidants were not affected regardless of the UV-C intensity. Consumer tests showed higher preference of fruit treated at high UV-C intensity. Results show that in addition to the applied dose, radiation intensity is a main factor determining the effectiveness of UV-C treatments and should not be over-sighted. For a given dose, increasing radiation intensity may in some cases maximize the benefits of UV-C on fruit quality, while significantly reducing the treatments time.     

Physiological basis of UV-C induced resistance to Botrytis cinerea in tomato fruit. V. Constitutive defence enzymes and inducible pathogenesis-related proteins

Changes in the protein content and profile of postharvest tomato fruit treated with the hormetic dose (3.7 kJ m^?2) of ultraviolet light C (UV-C) at the mature green stage was investigated. In UV-C treated fruits, the total protein content increased until 10 d after treatment and decreased thereafter during a 30 d storage period; whereas in control fruit, protein content decreased constantly throughout the storage period. Using polyacrylamide gel electrophoresis (PAGE) it was shown that UV-C treatment affected the protein profile of tomato fruit in several manners: (1) UV-C repressed the expression of some proteins presumably associated with ripening; (2) it enhanced the expression of several constitutive proteins, of which one was an acidic β-1,3-glucanase, three acidic chitinases and three basic chitinases; and (3) it induced the synthesis of at least 5 new proteins of which four were basic proteins. Among the proteins induced by UV-C, three (a basic β-1,3-glucanase and two acidic chitinases) were apparently pathogenesis-related proteins as they were also induced by inoculation with Botrytis cinerea. The molecular mass (MM) of five of the UV-C induced proteins was determined using SDS-PAGE. Their molecular masses were 45, 39.4, 34.6, 10 and 8.9 kDa. The UV-C induced β-1,3-glucanase had a MM of 33.1 kDa. The MM of two constitutive chitinases were 48.3 and 30.5 kDa, and those of the two UV-C and pathogenesis-induced chitinases were 37.1 and 20.6 kDa. Furthermore, the glucanohydrolase activities induced by UV-C were maintained until the end of the storage period. It is likely that the PR-proteins with glucanohydrolase activities induced by UV-C are an integral part of the long-term resistance observed in UV-C treated tomato fruit.     

Physiology of fresh-cut ‘Galia’ (Cucumis melo var. reticulatus) from ripe fruit treated with 1-methylcyclopropene

‘Galia’ (Cucumis melo var. reticulatus L. Naud. cv. Galia) fruit were harvested at the three-quarter slip stage and treated with 1 μL L⁻¹ 1-methylcyclopropene (1-MCP) at 20 °C for 24 h. The fruit were processed and stored as fresh-cut cubes and intact fruit for 10 d at 5 °C. Ethylene production of fresh-cut cubes was approximately 4–5-fold higher than intact fruit at day 1. Afterward, the ethylene production of fresh-cut cubes declined significantly whereas that of intact fruit remained relatively constant at about 0.69–1.04 ng kg⁻¹ s⁻¹. 1-MCP delayed mesocarp softening in both fresh-cut and intact fruit and the symptoms of watersoaking in fresh-cut fruit. Continuously stored fresh-cut cubes and cubes derived from intact fruit not treated with the ethylene antagonist softened 27% and 25.6%, respectively, during 10 d storage at 5 °C while cubes derived from 1-MCP-treated fruit softened 9% and 17%, respectively. Fresh-cut tissue from 1-MCP-treated fruit exhibited slightly reduced populations of both total aerobic organisms and Enterobacterium, although the differences did not appear to be sufficient to explain the differences in keeping quality between 1-MCP-treated and control fruit. Based primarily on firmness retention and reduced watersoaking, 1-MCP treatment deferred loss of physical deterioration of fresh-cut ‘Galia’ cubes at 5 °C by 2–3 d compared with controls.     

Evaluating the accuracy of VEMAP daily weather data for application in crop simulations on a regional scale

Weather plays a critical role in eco-environmental and agricultural systems. Limited availability of meteorological records often constrains the applications of simulation models and related decision support tools. The Vegetation/Ecosystem Modeling and Analysis Project (VEMAP) provides daily weather variables on a 0.5 latitude–longitude grid across the conterminous USA. Daily weather data from the VEMAP (1961–1990) for the state of Georgia were compared with data from 52 individual ground stations of the National Weather Service Cooperative Observer Program (COOP). Additionally, simulated crop grain yields of soybean (Glycine max) were compared using the two data sources. Averaged daily maximum and minimum temperatures (Tmax and Tmin, respectively), solar radiation (SRAD), and precipitation (PPT) differed by 0.2 °C, ?0.2 °C, 1.7 MJ m^?2 d^?1, and 0 mm, respectively. Mean absolute errors (MAEs) for Tmax, Tmin, SRAD, and PPT were 4.2 °C, 4.4 °C, 4.4 MJ m^?2 d^?1, and 6.1 mm, respectively, and root mean squared errors (RMSEs) for Tmax, Tmin, SRAD, and PPT were 5.5 °C, 5.9 °C, 5.8 MJ m^?2 d^?1, and 13.6 mm, respectively. Temperature differences were lowest during summer months. Simulations of grain yield using the two data sources were strongly correlated (r = 0.68, p < 0.01). The MAE of grain yield was 552 kg ha^?1. The RMSE of grain yield was 714 kg ha^?1. Hybrid analyses indicated that the variation of simulated yield was mainly associated with the differences in rainfall. The results showed that the VEMAP daily weather data were able to be adequately applied to crop growth simulation at spatial and temporal scales, especially for long-term climate change research. Overall, the VEMAP weather data appears to be a promising source for crop growth modeling concerned with scale to 0.5° coordinate grid.