The effects of ethylene aad ultraviolet (UV) (6,12). Several cell properties related to membranes have been reported to change with senescence. These include loss ofseveral membrane components (1, 2, 14), loss of semipermeability (12, 14), and a decrease in membrane lipid fluidity (3). Ethylene has been demonstrated to be directly involved in the regulation of flower senescence. Ethylene production increases sharply with senescence while exogenous application of ethylene enhanced flower senescence and wilting (6), increased permeability of petal cells (9, 14), and accelerated the decrease in cell membrane fluidity (15).Far-UV irradiation has been demonstrated to have several effects on plant cells. These include increase in cell membrane permeability (13), decrease in solute uptake capacity (5) raises the possibility of a common mechanism of action. The site of ethylene action is unknown, while that of UV irradiation might be more clearly identified physically. Therefore, a detailed comparison between the effects of these two agents might lead to a better understanding of senescence processes.
MATERIALS AND METHODS Plant Material. Carnation flowers (Dianthus caryophyllus L. cvWhite Sim) were grown, harvested at the fully open stage, and prepared as outlined previously (11). Treatments with UV irradiation and ethylene were given 2 h after harvest and for the periods specified. Treatments and evaluations were carried out at 21°C, RH 75 ± 5%, and unless otherwise specified, at light intensity of Chemical Treatments. Ethylene was applied to the flowers at 10 ,4/l for 6 h as described previously (11). Silver thiosulfate was applied as a pulse treatment through the stems for 10 min at 4 mm as described by Reid et al. (10). Petal In-Rolling. Wilting of the flower petals was monitored by measuring the in-rolling of the petal tips. This was measured as the angle through which the petal tip had rolled, relative to the plane of the petal base.Petal Eletrolyte Leakage. The leakage of electrolytes from the petals into a 0.5 M mannitol bathing solution was measured essentially as described by Suttle and Kende (14). Ten petals were washed for 10 min and placed into 10 ml bathing solution for 10 h at 30°C. The conductivity ofthe resulting solution was measured using a Radiometer Copenhagen CDM 2e conductivity meter.Ethylene Measurements. Ethylene production by whole flowers was measured as described previously (11). Ethylene production of isolated petals was measured by sealing them in quartz cuvettes of 3.5 ml volume from which samples were taken at 15-intervals for ethylene determinations. After each sampling, the cuvettes were aerated with ethylene-free air.Sucrose Uptake.