Fruit of `Redchief Delicious' apple [Malus sylvestris (L) Mill. var. domestica (Borkh.) Mansf.] were harvested 1 week before the climacteric (harvest 1), at the onset of the climacteric (harvest 2), and 1 week after the onset of the climacteric (harvest 3). Fruit were stored at 0, 5, 10, 15, or 20 °C and were treated with 0.7 μL·L-1 1-MCP on a once-per-week, once-per-2-week, once-per-month, and once-per-year basis or were left nontreated. The initial 1-MCP treatment was at 20 °C and subsequent applications were at storage temperatures. The compound slowed softening at all temperatures relative to nontreated fruit, however as temperature decreased, the benefits of 1-MCP application became less pronounced. Effectiveness of 1-MCP declined slightly as harvest maturity increased. Efficacy of 1-MCP treatment increased with greater frequency of application at 5, 10, 15, and 20 °C, but not at 0 °C. Fruit stored without refrigeration (20 °C) for more than 100 days did not soften significantly when treated once per week with 1-MCP. However, decay was a significant problem for treated and nontreated fruit stored at temperatures >5 °C; 1-MCP application reduced, but did not prevent decay. Rate of decline in titratable acidity increased with storage temperature and 1-MCP had no significant effect on retarding the decline in acid content. Minimal (Fo) and maximal (Fm) chlorophyll fluorescence was altered markedly by 1-MCP application, but the ratio of (Fm-Fo)/Fm was only slightly affected. The most effective 1-MCP treatment frequency was once per week and, at all elevated temperatures (5, 10, 15, and 20 °C), slowed loss of firmness to a greater extent than refrigeration (0 °C) alone. Application of 1-MCP resulted in greater retention of firmness than controlled atmosphere (CA) with O2 and CO2 at 1.5 kPa and 3 kPa, respectively. Data suggest that 1-MCP application, has the potential to reduce reliance on refrigeration and CA storage for maintaining firmness of `Redchief Delicious' apple, especially for relatively short storage durations (<50 days) when fruit are harvested within a week of the ethylene climacteric. Chemical name used: 1-methylcyclopropene (1-MCP).

The capacity for 1-methylcyclopropene (1-MCP) to inhibit color change and firmness loss and alter aroma profiles for tomato (Lycopersicon esculentum Mill.) fruit was evaluated as a function of 1-MCP concentration, multiple and continuous applications, and stage of ripeness. In addition, the relationship between external and internal fruit color and firmness was determined. 1-MCP reduced the rate of red color development in fruit of all stages of ripeness. A single application of 1-MCP delayed color development by ≈ days. A second application of 1-MCP 10 days after first treatment additionally delayed color development of mature green fruit by another 8 to 10 days. Continuous 1-MCP application completely inhibited color development of breaker and half-ripe fruit for the duration (34 days) of application, but only partially inhibited firmness loss. When fruit at 50% color development were treated with 1-MCP, gel color development tended to lag behind the external fruit color change compared to nontreated fruit. Some aroma volatiles were affected by 1-MCP applied at the mature green and breaker stages, but the effect was relatively minor; 1-MCP did not affect sugar or titratable acid levels in these fruit. Collectively, the data indicate 1-MCP caused minor shifts in the quality attributes of locule color, aroma, and firmness relative to external color, which may reduce the value of this treatment, but benefits accrued by slowed firmness loss and color development may afford sufficient compensation to make 1-MCP application commercially feasible.

No abstract

The CO2 and HCO3" fluxes in air-grown cells of Synechococcus UTEX 625 at pH 8-0 were measured during dark to light and light to dark transitions using a mass spectrometer and sampling of the reaction medium. The kinetic parameters for initial uptake of CO2 aud HCO3" were determined during the initial period of illumination. The development of the internal Cj pool was followed up to steady-state photosynthesis, which occurred when the size of the internal inorganic carbon pool remained apparently constant for a limited period. The experimental procedure confirmed that only CO2 transport occurred with lOOmmolm •* Na^ and that hoth CO2 and HCO3" transport occurred with 25 mol m"-^ Na"*". The K1/2 values of initial CO2 and HCO3" uptake were 0-7 and 17-2 mmol m~^ respectively and agreed closely with the K1/2 values of net CO2 and HCO3 transport during steady-state photosynthesis, which were 0-66 and 17-1 mmolm ^ respectively. Maximum rates of CO2 and HCO3" transport were 423 and 219 mmol h ' g"' Chi. Maximum CO2 efflux observed upon darkening was 118mmolh 'g"' Chi. A permeability coefficient of the cell for CO2 of 3 X 10" tn s"' was determined from the dark CO2 efflux assuming an internal pH of 7-2 in the dark. Following the initial CO2 uptake in the light, the extracellular [CO2] steadily declined when only CO2 transport was allowed, but an increase in the extracellular [CO2] when HCO3" transport was allowed to proceed suggested that an ettihanced CO2 efflux occurred as a result of the larger size of the intracellular C| pool.

`Cortland' apples (Malus ×domestica Borkh.), either untreated or treated with diphenylamine (DPA), were stored for 120 days in air at 0 °C. Peel samples were taken from these fruit immediately after storage, placed in glass vials and incubated for 48 hours, or were isolated from fruit held 2 to 72 hours at 22 °C and incubated in the vials for 2 hours. Emission of 3,7,11-trimethyldodeca-1,3(E),6(E),10-tetraene, known as trans,trans-α-farnesene, or simply α-farnesene, and its oxidation product, MHO, were measured in the vial headspace. α-Farnesene content in the gas phase of vials with peel samples reached a maximal level 2 hours after vials were sealed and was higher in DPA-treated than untreated fruit. The content of α-farnesene in the vial headspace remained unchanged for DPA-treated fruit peel during the 2-day holding period. However, α-farnesene declined rapidly after 10 hours incubation for control samples. Incubating peel samples of control fruit under N2 atmosphere prevented the decline in α-farnesene. The MHO release by the peel of control fruit was rapid during the first 2 hours and continued to increase for 24 hours. In contrast, the MHO released from DPA-treated fruit peels was 8000-fold lower than from peel samples of control fruit. The increase in vapor phase MHO was concomitant with peel browning in controls. For whole fruit held at 22 °C for 2 to 72 hours, cumulative MHO release from fruit peels followed a pattern that was similar to the pattern of superficial scald development in these fruit.