首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
Temperatures up to 35°C have been shown to increase ethylene production and ripening of propylene-treated kiwifruit (Stavroulakis, G., Sfakiotakis, E.M., 1993. We attempted to study the regulation by high stress temperature of the propylene induced ethylene biosynthesis and ripening in ‘Hayward’ kiwifruit. ‘Hayward’ kiwifruit were treated with 130 μl/l propylene at temperatures from 30 to 45°C up to 120 h. Ethylene biosynthesis pathway and fruit ripening were investigated. Propylene induced normal ripening of kiwifruit at 30–34°C. Fruit failed to ripe normally at 38°C and above 40°C ripening was inhibited. Propylene induced autocatalytic ethylene production after a lag period of 24 h at 30–34°C. Ethylene production was drastically reduced at 38°C and almost nil at 40°C. The 1-aminocyclopropane-1-carboxylic acid (ACC) content was similar at 30–38°C and was very low at 40°C. The 1-aminocyclopropane-1-carboxylate synthase (ACC synthase) and 1-aminocyclopropane-1-carboxylate oxidase (ACC oxidase) activities decreased with a temperature increase above 30°C, but ACC oxidase decreased at a faster rate than ACC synthase. Fruit not treated with propylene showed no ripening response or ethylene production. However, kiwifruit respiration rate increased with temperature up to 45°C, reaching the respiration peak in 10 h. At temperatures up to 38°C, propylene treatment enhanced the respiration rate. After 48 h at 45°C, fruit showed injury symptoms and a larger decrease in CO2. The results suggest that high temperature stress inhibits ripening by inhibiting ethylene production and sensitivity while respiration proceeds until the breakdown of tissues.  相似文献   

2.
The effect of delays of 1, 5, 10 or 15 d after harvest in establishing a static controlled atmosphere (SCA) or dynamic controlled atmosphere (DCA) on the quality of ‘Hass’ avocados (Persea americana Mill.) was investigated. Fruit were stored at 5 °C in SCA (5% O2/5% CO2) or DCA (<3% O2/0.5% CO2) for 6 weeks and compared with fruit stored in air. In addition, to determine whether increasing the CO2 in the DCA would affect the fruit quality, DCA-stored fruit were compared with fruit held in a DCA with 5% CO2 (DCA + CO2) established 1 d after harvest. The quality of fruit was assessed at the end of storage and after ripening at 20 °C. DCA-stored fruit ripened in 4.6 d compared with 7.2 d for SCA-stored fruit, or 4.8 d for air-stored fruit. In addition, the incidences of stem end rot (SER), body rot (BR) and vascular browning (VB) were lower in DCA-stored fruit (35%, 29% and 29%, respectively) than in SCA-stored fruit (57%, 52% and 49%, respectively), or air-stored fruit (76%, 88% and 95%, respectively). Delaying the establishment of both SCA and DCA for 15 d resulted in significantly more advanced skin colour at the end of storage (average rating score 11.9) compared with other delay periods (4.6–5.1). There was no significant effect of delay on the time to ripen, skin colour when ripe or any ripe fruit disorder incidence. The incidence of diffuse flesh discolouration (DFD) was not only <1% when averaged over all delays but only occurred at >0.5% incidence in the 15 d delay treatment in DCA (4.8%) and not in SCA. The incidence of diffuse flesh discolouration was 62% in air-stored fruit. Inclusion of 5% CO2 in DCA retarded fruit ripening from 4.7 to 6.9 d and increased the incidence of rots at the end of storage from 5% to 14%, and increased the incidence in ripe fruit of SER from 30% to 56% and of BR from 27% to 55%. It is concluded that fruit quality was better after CA storage than after air storage, and that DCA storage was better than SCA. The effect of DCA is to independently reduce the time to ripen after storage and the incidence of rots when ripe. Delaying the application of SCA or DCA did not affect the expression of rots, but may increase the incidence of DFD. Inclusion of CO2 at 5% in CA retarded fruit ripening but stimulated rot expression and should not be used for CA storage of New Zealand grown ‘Hass’ avocados.  相似文献   

3.
'Laiyang Chili’ and ‘Ya Li’ (Pyrus bertschneideri Reld) pears were treated with 3, 6, and 9% emulsions of commercial or refined (reduced -tocopherol levels) plant (soybean, corn, peanut, linseed, and cottonseed) oils at harvest an stored at 0°C for 6 months. Effects of oil treatments on ethylene production, respiration, fruit firmness, fruit color, soluble solid content (SSC), titratable acids (TA), internal browning (IB), and internal CO2, O2, and ethanol were studied. At the same concentration, oil treatments induced similar responses regardless of their sources or their -tocopherol concentrations. In both cultivars, ethylene production and respiration in fruit treated with 9% oils were lower in early storage and higher in late storage than that in the controls. Oils at 6% reduced IB, at 9% inhibited IB completely, and at 3% was not effective after 6 months at 0°C and 7 days at 20°C. Plant oil treatment maintained fruit color, firmness, SSC, and TA in a concentration-dependent manner during storage. In the first 4 months storage, 9% corn oil-treated fruit contained similar partial pressure of CO2 and O2 as the controls. After 5 months storage, oil-treated fruit contained higher partial pressure of CO2 and lower levels of O2 than the controls. When held at 20°C for 7 days, changes of internal CO2 and O2 were slower but partial pressure of CO2 were higher, and O2 were lower, in 9% corn oil-treated fruit than in the controls. Internal ethanol was not affected by oil treatment compared with control, either during storage or 7 days at 20°C. No off-flavor was detected in either oil-treated and control fruit by sensory evaluation.  相似文献   

4.
Potato (Solanum tuberosum L cv. Bintje) was exposed to ambient and elevated carbon dioxide (CO2), to ambient and elevated ozone (O3) and to elevated levels of both gases during two growing seasons, 1998 and 1999. Experiments in open-top chambers (OTC) were carried out in Finland, Sweden, Ireland, United Kingdom, Germany and Belgium and a FACE (Free Air Carbon dioxide Enrichment) experiment was carried out in Italy. In OTCs the plants were grown under ambient CO2 concentrations or with 550 and 680 μl l−1 CO2 alone or in combination with ambient or elevated O3 concentrations (target seasonal mean of 60 nl l−1 8 h per day). In the FACE systems the plants were exposed to ambient or 550 μl l−1 CO2. In the OTC experiments the reducing sugar content of potato tubers decreased significantly with increased concentration of O3. The starch content of potato tubers decreased, with negative impact on tuber quality, but the ascorbic acid concentration increased as a function of the AOT40 (The sum of the differences between hourly ozone concentration and 40 nl l−1 for each hour when the concentration exceeds 40 nl l−1 during a relevant growing season). However, simultaneous exposure to elevated CO2 counteracted the ozone effect. With increase in the CO2 exposure, glycoalkaloid and nitrate concentrations decreased yielding improved quality, while the citric acid concentration decreased causing a higher risk for discoloration after cooking. The amount of dry matter and starch increased significantly in the FACE experiment.  相似文献   

5.
The response of cabbage to controlled atmospheres (CA) of 1–3% O2 and 1–10% CO2; 3% O2 and 5% CO2 was studied in relation to the incidence of physiological and pathological disorders. Fungal infections, pepper spot, low oxygen injury, weight loss, colour, odour, flavour and ethanol were evaluated. The findings show that CA did not reduce Botrytis cinerea rot in comparison to low temperature storage in air. PVC film and CA, on the other hand, reduced pepper spot by over 50% with respect to the air control. In particular, pepper spot was eliminated by high CO2 (10%) levels. Low O2 (1% O2 and 1% CO2) atmospheres caused 33 and 50% injury respectively after 89 and 109 days of storage. CA and PVC film reduced weight loss to 1%, as compared with 11% in the heads in air, which had shrivelled. The combination of 3% O2/5% CO2 and PVC film delayed yellowing with respect to air control. Concentrations of 1–3% O2 and 10% CO2 resulted in off odours and flavours after 74 days of storage. This result was confirmed by a considerable increase in ethanol concentrations. The most effective concentration tested was 3%O2/5%CO2 although, in general, infection by B. cinerea limited the storage life.  相似文献   

6.
Modified atmosphere packaging alleviates chilling injury in cucumbers   总被引:7,自引:0,他引:7  
Cucumbers (Cucumis sativus L.) packaged in perforated or sealed 31.75 μm (1.25 mil) low density polyethylene (LDPE) bags were found to have less severe chilling injury than nonwrapped fruit in storage at 5 °C and 90–95% relative humidity. The onset of chilling injury was also delayed by the LDPE packaging compared to the nonpackaged control. The concentrations of CO2 increased to 3% while O2 levels decreased to 16% in the sealed bags. Fruit in the sealed bags had the least decay. The O2 and CO2 concentrations inside the perforated bags changed very little from the ambient atmosphere. However, there was a marked difference in the weight loss between nonwrapped cucumbers and fruit from perforated or sealed bags. The weight loss of nonwrapped fruit reached 9% in 18 days while perforated and sealed samples lost less than 1% during the same period. Chilling stress induced increases in putrescine levels in all treatments but the sealed fruit had the highest levels of putrescine. Sealed fruit and perforated fruit also had higher content of spermidine than non-wrapped fruit. These high levels of polyamines may have contributed to the increase of chilling tolerance in fruit from perforated and sealed packages.  相似文献   

7.
Central to the CHanging climate and potential Impacts on Potato yield and quality project (CHIP) was the consideration of the potential impacts of ozone and CO2 on growth and yield of future European Potato crops. Potato crops, cv. Bintje, were exposed to ambient or elevated ozone; targeted daily average, 60 nl l−1 for 8 h, and ambient or elevated CO2; targeted 680 μl l−1 averaged over the full growing season, in open top chambers (OTCs) at six European sites in 1998 and 1999, or to elevated CO2 (550 μl l−1) in Free Air Carbon dioxide Enrichment facilities (FACE) at two sites in both years. Some OTC experiments included 550 μl l−1. Above and below ground biomass were measured at two destructive harvests; at maximum leaf area (MLA) and at final-harvest. Final-harvest fresh weight yields of marketable-size tubers, >35 mm diameter, from ambient conditions ranged from 1 to 12 kg m−2. There was no consistent (P>0.1) CO2×O3 interaction for growth or yield variables at either harvest. No consistent effects of ozone were detected at the maximum-leaf-area harvest. However, at final harvest, ozone had reduced both above-ground biomass and tuber dry weight (P<0.05), particularly of the largest (>50 mm) size class. These yield losses showed linear relationships both with accumulated ozone exposure; AOT40 expressed as nl l−1 h over 40 nl l−1, and with yields from chambered ambient-ozone treatments (P<0.05) but, because of partial confounding between the treatment AOT40s and the ambient-ozone yields in the data, the two relationships were not completely independent. Yields from ambient-ozone treatments, however, explained a significant (P<0.01) amount of the residual variation in ozone effects unexplained by AOT40. When averaged over all experiments, mean dry weights and tuber numbers from both harvests were increased by elevated CO2. Only green leaf number at the MLA harvest was reduced. The CO2 responses varied between sites and years. For marketable-size tubers, this variation was unrelated to variation in ambient-CO2 treatment yields. Yield increases resulting from the 680 μl l−1 and 550 μl l−1 treatments were similar. Thus elevating [CO2] from 550 to 680 μl l−1 was less effective than elevating [CO2] from ambient to 550 μl l−1. On average, CO2 elevation to 680 μl l−1 increased the dry weight of marketable-size tubers by about 17%, which far exceeded the average ozone-induced yield loss of about 5%. The net effect of raising CO2 and O3 concentrations on the European potato crop would be an increase marketable yield.  相似文献   

8.
This paper describes the effects of elevated CO2 (550 and 680 μl l−1) and O3 (60 nl l−1 O3 as an 8 h mean), alone or in combination, on canopy development and senescence in potato (Solanum tuberosum L. cv Bintje) across a range of European agro-climatic conditions. The assessments were made within the European CHIP project (CHanging climate and potential Impacts on Potato yield and quality) that was conducted for two growing seasons (1998 and 1999) in free air CO2 enrichment systems (FACE) and open-top chamber facilities (OTCs) at seven European sites. A comparison of chambered and unchambered experimental plots was included to examine the effects of chamber enclosure. Phenological growth stages, plant height, leaf area index (LAI) and the number of green and yellow leaves were recorded non-destructively throughout the growing season and by a destructive intermediate harvest at maximum leaf area (MLA). In the dynamic growth analysis CO2 and O3 effects were studied over three developmental stages: canopy expansion, full canopy and canopy senescence. Chamber enclosures promoted potato crop development (taller plants, more leaves) during the initial growth stages and led to a faster decline of LAI and a higher number of yellow leaves. The growth in ambient plots varied between sites and seasons, as did the scale of the treatment responses. Despite the large background variation, some overall treatment effects could be detected across all sites. Both levels of increased CO2 reduced final plant height in comparison to ambient concentrations, which indicates a premature ending of the active plant growth. At the stage of full canopy and crop senescence the average number of green leaves was significantly (P<0.05) decreased by 680 μl l−1 CO2 (OTC experiments) and LAI showed the same tendency (P=0.07). As there was however no indication of a decreased leaf formation during initial growth and at full canopy, this must have been due to an earlier leaf fall. In the FACE experiments LAI had already began to decline at the stage of full canopy at 550 μl l−1 CO2 but not in ambient CO2 (DAE×CO2, P<0.05). These observations strongly indicated that elevated CO2 induced a premature senescence during full canopy. O3 did not have an overall detrimental effect on crop development during initial growth nor at full canopy, but did induce a faster reduction of LAI during crop senescence (DAE×O3, P<0.05). Final plant height was not affected by O3. There were few CO2×O3 interactions detected. There was a suggestion (P=0.06) that O3 counteracted the CO2-induced decrease of green leaves at full canopy, but on the other hand during crop senescence the decline of LAI due to elevated O3 was faster at ambient compared to elevated CO2 (P<0.05). These responses of canopy development to elevated CO2 and O3 help to explain the treatment responses of potato yield within the CHIP project at sites across Europe.  相似文献   

9.
以酥梨为试材,研究了(0±0.5)℃条件下不同O2浓度梯度和CO2浓度梯度的气调贮藏对酥梨采后生理及果实褐变的影响。结果表明:在贮藏期内,当CO2浓度为0%时,随着O2浓度的降低,在一定程度上可以延缓酥梨果肉组织相对电导率的升高、酚类物质的下降、多酚氧化酶活性的上升及色泽的转黄;但当O2浓度为1.5%时,会对酥梨果实造成伤害,引起多酚氧化酶活性上升,果心褐变指数升高;当O2浓度为5%时,CO2浓度的升高有效保持了果实的硬度、色泽;但当CO2浓度为8%时,会导致酥梨果实相对电导率增幅加大,果心、果肉酚类物质氧化加剧,果心褐变指数升高。综上所述,酥梨适宜的气调指标阈值为CO2<2%,O2为3%~5%。  相似文献   

10.
Spring wheat cv. Minaret crop stands were grown under ambient and elevated CO2 concentrations at seven sites in Germany, Ireland, the UK, Belgium and the Netherlands. Six of the sites used open-top chambers and one used a controlled environment mimicking field conditions. The effect of elevated CO2 for a range of N application regimes, O3 concentrations, and growth temperatures on flag leaf photosynthesis was studied. Before anthesis, flag leaf photosynthesis was stimulated about 50% by 650 compared with 350 μmol mol−1 CO2 at all sites, regardless of other treatments. Furthermore, there was no evidence of a decrease in photosynthetic capacity of flag leaves due to growth at elevated CO2 before anthesis, even for low N treatments. However, photosynthetic capacity, particularly carboxylation capacity, of flag leaves was usually decreased by growth at elevated CO2 after anthesis, especially in low N treatments. Acclimation of photosynthesis to elevated CO2 therefore appears to occur only slowly, consistent with a response to changes in sink–source relationships, rather than a direct response. Effect of elevated CO2 on stomatal conductance was much more variable between sites and treatments, but on average was decreased by ˜10% at 650 compared with 350 μmol mol−1 CO2. Carboxylation capacity of flag leaves was decreased by growth at elevated O3 both before and after anthesis, regardless of CO2 concentration.  相似文献   

11.
Ethylene biosynthesis in kiwifruit, Actinidia chinensis ‘Sanuki Gold’ was characterized using propylene, an ethylene analog, and 1-methylcyclopropene (1-MCP), an inhibitor of ethylene perception. In fruit harvested between a young stage (66 days after pollination) (DAP) and an early commercial harvesting stage (143 DAP), 2 days of exposure to propylene were sufficient to initiate ethylene biosynthesis while in fruit harvested at commercial harvesting stage (154 DAP), 4 days of propylene treatment were required. This observation suggests that response of ethylene biosynthesis to propylene treatment in kiwifruit declined with fruit maturity. Propylene treatment resulted in up-regulated expression of AC-ACO1, AC-ACO2, AC-SAM1 and AC-SAM2, prior to the induction of AC-ACS1 and ethylene production, confirming that AC-ACS1 is the rate limiting step in ethylene biosynthesis in kiwifruit. Treatment of fruit with more than 5 μL L?1 of 1-MCP after the induction of ethylene production subsequently suppressed ethylene production and expression of ethylene biosynthesis genes. Treatment of fruit with 1-MCP at harvest followed with propylene treatment delayed the induction of ethylene production and AC-ACS1 expression for 5 days. These observations suggest that in ripening kiwifruit, ethylene biosynthesis is regulated by positive feedback mechanism and that 1-MCP treatment at harvest effectively delays ethylene production by 5 days.  相似文献   

12.
The physiological effects of elevated CO2 and/or O3 on Solanum tuberosum cv. Bintje were examined in Open-Top Chambers during 1998 and 1999 at experimental sites across Europe as part of the EU ‘Changing Climate and Potential Impacts on Potato Yield and Quality’ programme (CHIP). At tuber initiation (≈20 days after emergence, DAE) elevated CO2 (680 μl l−1) induced a 40% increase in the light saturated photosynthetic rate (Asat) of fully expanded leaves in the upper canopy. This was 16% less than expected from short-term exposures of plants grown under ambient CO2 (360 μl l−1) to elevated CO2, indicating that photosynthetic acclimation began at an early stage of crop growth. This effect resulted from a combination of a 12% reduction in stomatal conductance (gs) and a decline in photosynthetic capacity, as indicated by the significant reductions in the maximum carboxylation rate of Rubisco (Vcmax) and light-saturated rate of electron transport (Jmax) under elevated CO2. The seasonal decline in the promotion of photosynthesis by elevated CO2 reflected the concurrent decrease in gs. Vcmax and Jmax were both reduced in plants grown under elevated CO2 until shortly after maximum leaf area (MLA) was attained. Although non-photorespiratory mitochondrial respiration in the light (Rd) increased during the later stages of the season, net photosynthesis was consistently increased by elevated CO2 during the main part of the season. Photosynthetic rate declined more rapidly in response to elevated O3 under ambient CO2, and the detrimental impact of O3 was most obvious after MLA was attained (DAE 40–50). Several exposure indices were compared, with the objective of determining the critical ozone level required to induce physiological effects. The critical O3 exposure above which a 5% reduction in light saturated photosynthetic rate may be expected (expressed in terms of cumulative exposure above 0 nl l−1 O3 between emergence and specific dates during the season (AOT0-cum)) was 11 μl l−1 h; however this value should only be extrapolated beyond the CHIP dataset with caution. The interaction between O3 and stomatal behaviour was more complex, as it was influenced by both long-term and daily exposure levels. Elevated CO2 counteracted the adverse effect of O3 on photosynthesis, perhaps because the observed reduction in stomatal conductance decreased O3 fluxes into the leaves. The results are discussed in the context of nitrogen deficiency, carbohydrate accumulation and yield.  相似文献   

13.
Potato cv. Bintje was grown in open-top-chambers and free-air-CO2-enrichment systems at 7 sites across Europe for 2 years (1998–99). The effect of different treatments (CO2 enrichment and O3 fumigation) on the chlorophyll content of fully expanded upper and lower canopy leaves was investigated collecting Minolta SPAD-502 meter readings. In both CO2 treated and O3 fumigated plants, leaves had lower chlorophyll content than those in ambient air controls; season-long chlorophyll averages were 9.3% lower in the ‘CO2’ treatments, 9.1% lower in ‘O3’ treatments and 12.3% lower in ‘CO2+O3’ treatments. The analysis of chlorophyll content in three different growth phases (Emergence–Tuber Initiation; Tuber Initiation–Maximum Leaf Area; Maximum Leaf Area–Harvest) showed that in the early growth period, i.e. before tuber initiation there was a slight indication for an higher chlorophyll content at elevated CO2 (+3.8%) or O3 (+1.7%). However, from tuber initiation onwards the leaves of plants grown under elevated CO2 or O3 showed a progressively lower chlorophyll content (−4.8% for CO2 treatments and −2.6% for O3 treatments) indicating a faster senescence of leaves that increased during the late growth period (−12.8% for CO2 treatments and −12.7% for O3 treatments) and that was enhanced by CO2–O3 interaction (−17.8%).  相似文献   

14.
The influence of aqueous 1-methylcyclopropene (1-MCP) concentration, immersion duration, and solution longevity on the ripening of early ripening-stage tomato (Solanum lycopersicum L.) has been investigated. Tomato fruit at the breaker-turning stage were fully immersed in aqueous 1-MCP at 50, 200, 400 and 600 μg L−1 for 1 min, quickly dried, and then stored at 20 °C. Ethylene production, respiration, surface color development, and rate of accumulation of lycopene and polygalacturonase (PG) activity were suppressed and/or delayed in fruit exposed to aqueous 1-MCP. Suppression of ripening was concentration dependent, with maximum inhibition in response to 1 min immersion occurring at concentrations of 400 and 600 μg L−1. Climacteric ethylene peaks were delayed approximately 6, 7, and 9 d and respiration was strongly suppressed in fruit treated with aqueous 1-MCP at 200, 400, and 600 μg L−1, respectively, compared with control fruit. Fruit firmness, lycopene content, PG activity, and surface hue of fruit treated at the three higher levels remained strongly suppressed compared with control. Skin hue values and pericarp lycopene content in response to treatment at the subthreshold 50 μg L−1 provided evidence for differential ripening suppression in external versus internal tissues. Maximum delay of softening and surface color development in response to 50 μg L−1 aqueous 1-MCP occurred following immersion periods of between 6 and 12 min. Factors affecting fruit penetration by aqueous 1-MCP and mechanisms contributing to recovery from 1-MCP-induced ripening inhibition are discussed.  相似文献   

15.
Controlling the rate of fruit softening in melting-flesh peaches is a primary goal of the fruit industry. Stony hard (SH) peach varieties lack the ability to synthesize 1-aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, which is required for fruit maturation. SH peaches thus have crisp flesh that remains firm during ripening. In this study, we developed a simple technique to stimulate fruit softening by a single spray application of ACC at a concentration of 10–20 mM, which was sufficient to allow ethylene synthesis and fruit softening. Higher concentrations of ACC increased ethylene production, and made the fruit softer. Ethylene synthesis was limited to the first 2–3 d after ACC treatment, after which fruit ceased softening and retained its remaining firmness. These results indicate that a single application of ACC solution can be used to regulate the process of fruit softening in SH peaches.  相似文献   

16.
Storage of ‘Fuji’ apple fruit in a high CO2 (3 kPa) and low O2 (1.5 kPa) controlled atmosphere (CA) reduced firmness and titratable acidity (TA) loss during long term storage. This CA environment also induced development of internal CO2-injury (brown-heart) and slowed the disappearance of watercore. The symptoms of internal CO2-injury were first detected 15 days after CA establishment and the severity increased during the first 4 months of CA-storage. Delaying establishment of CA conditions for 2–12 weeks significantly reduced the severity of CO2-injury. Delaying CO2 accumulation to 3 kPa for 1–4 months during CA (1.5 kPa O2+0.05 kPa CO2) storage also reduced development of CO2-injury symptoms. Delaying CA or CO2 accumulation resulted in lower firmness and TA compared to establishment of CA within 72 h of harvest. However, the delay treatments did result in firmness and TA that were significantly higher compared to values for fruit stored in air. The incidence and severity of senescent injuries (flesh browning and core flush) detected during the late period of storage were greater in air- than CA-stored fruit. The results indicate the susceptibility of ‘Fuji’ apples to CO2-injury is highest during the first weeks of storage after harvest. Delaying establishment of CA or exposure to elevated CO2 after harvest may be a practical strategy to reduce CO2-injury while maintaining other important quality attributes at acceptable levels.  相似文献   

17.
One of the major goals of the European Stress Physiology and Climate Experiment (ESPACE-wheat) was to investigate the sensitivity of wheat growth and productivity to the combined effects of changes in CO2 concentration, ozone and other physiological stresses. Experiments were performed at different sites throughout Europe, over three consecutive growing-seasons using open-top chambers. This paper summarizes the main experimental findings of the effects of CO2 enrichment and other factors i.e. ozone (O3), drought stress or nitrogen supply on the biomass and yield of spring wheat (Triticum aestivum cv. Minaret). Final harvest data from different sites and seasons were statistically analysed: (1) to identify main effects and interactions between experimentally controlled factors; and (2) to evaluate quantitative relationships between environmental variables and biological responses. Generally, ‘Minaret’ wheat did not respond significantly to O3, suggesting that this cultivar is relatively tolerant to the O3 levels applied. The main effect of CO2 was a significant enhancement of grain yield and above-ground biomass in almost all experiments. Significant interactions between CO2 and other factors were not common, although modifications in different N- and water supplies also led to significant effects on grain yield and biomass. In addition, climatic factors (in particular: mean air temperature and global radiation) were identified as important co-variables affecting grain yield or biomass, repectively. On average, the yield increase as a result of a doubling of [CO2] was 35% compared with that observed at ambient CO2 concentrations. However, linear regressions of grain yield or above-ground biomass for individual experiments revealed a large variability in the quantitative responses of ‘Minaret’ wheat to CO2 enrichment (yield increase ranging from 11 to 121%). Hence, CO2 responsiveness was shown to differ considerably when the same cultivar of wheat was grown at different European locations. Multiple regression analyses perfomed to evaluate the relative importance of the measured environmental parameters on grain yield indicated that although yield was significantly related to five independent variables (24 h mean CO2 concentration, 12 h mean O3 concentration, temperature, radiation, and drought stress), a large proportion of the observed variability remained unexplained.  相似文献   

18.
The mode of action of nitric oxide (NO) in inhibiting ethylene biosynthesis and fruit softening during ripening and cool storage of mango fruit was investigated. Hard mature green mango (Mangifera indica L. cv. ‘Kensington Pride’) fruit were fumigated with 20 μL L−1 NO for 2 h at 21 °C and allowed to ripen at 21 ± 1 °C for 10 d, or stored at 13 ± 1 °C for 21 d. During ripening and cool storage, ethylene production and respiration rate from whole fruit were determined daily. The 1-aminocyclopropane-1-carboxylic acid (ACC) content, activities of ACC synthase (ACS), ACC oxidase (ACO), and fruit softening enzymes such as pectin esterase (PE), endo-1,4-β-d-glucanase (EGase), exo- and endo-polygalacturonase (exo-PG, endo-PG) as well as firmness and rheological properties of pulp were determined at two- and seven-day intervals during ripening and cool storage, respectively. NO fumigation inhibited ethylene biosynthesis and respiration rate, and maintained higher pulp firmness, springiness, cohesiveness, chewiness, adhesiveness, and stiffness. NO-fumigated fruit during cool storage and ripening had lower ACC contents through inhibiting the activities of both ACS and ACO in the fruit pulp. NO-fumigated fruit showed decreased activities of exo-PG, endo-PG, EGase, but maintained higher PE activity in pulp tissues during ripening and cool storage. In conclusion, NO fumigation inhibited ethylene biosynthesis through inhibition of ACS and ACO activities leading to reduced ACC content in the fruit pulp which consequently, reduced the activities of fruit softening enzymes during ripening and cool storage.  相似文献   

19.
Controlling the rate of fruit softening in melting-flesh peaches is a primary goal of the fruit industry. Stony hard (SH) peach varieties lack the ability to synthesize 1-aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, which is required for fruit maturation. SH peaches thus have crisp flesh that remains firm during ripening. In this study, we developed a simple technique to stimulate fruit softening by a single spray application of ACC at a concentration of 10–20 mM, which was sufficient to allow ethylene synthesis and fruit softening. Higher concentrations of ACC increased ethylene production, and made the fruit softer. Ethylene synthesis was limited to the first 2–3 d after ACC treatment, after which fruit ceased softening and retained its remaining firmness. These results indicate that a single application of ACC solution can be used to regulate the process of fruit softening in SH peaches.  相似文献   

20.
Spring wheat cv. Minaret was grown in open-top chambers at four sites across Europe. The effect of different treatments (CO2 enrichment, O3 fumigation, drought stress and temperature) on the chlorophyll content of the flag leaf was investigated using the MINOLTA SPAD-502 meter. Under optimum growth conditions the maximum chlorophyll content, which was reached at anthesis, was consistent among the sites ranging from 460 to 500 mg chlorophyll m−2. No significant effect of elevated CO2 or O3 was observed at anthesis. Leaf senescence, indicated by the chlorophyll breakdown after anthesis, was relatively constant in the control chambers. Under control conditions, thermal time until 50% chlorophyll loss was reached was 600°C day. Elevated CO2 caused a faster decline in chlorophyll content (thermal time until 50% chlorophyll loss was reduced to 500–580°C day) indicating a faster rate of plant development at two experimental sites. The effect of ozone on chlorophyll content depended on the time and dose of O3 exposure. During grain filling, high O3 concentrations induced premature senescence of the flag leaves (up to −130°C day). This deleterious effect was mitigated by elevated CO2. Drought stress led to faster chlorophyll breakdown irrespective of CO2 treatment.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号