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Susan S. Han

Leaf yellowing of excised Easter lily leaves was significantly delayed by application of gibberellic acids ≥250 mg·liter-1 or benzyladenine ≥50 mg·liter-1. Rapid development of foliar chlorosis following cold storage was delayed significantly by applying 500 mg·liter-1 of GA3 or BA before storage. Poststorage treatments were less effective. Development of chlorosis was associated with rapid loss of fresh weight and was not related to the aperture of the stomates (diffusive resistance). Respiration rates of leaves treated with growth regulators were significantly lower than those of the controls.'

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R.C. Beeson Jr.

Elaeagnus pungens Thunb., Ligustrum japonicum Thunb., Photinia ×fraseri `Red Top', and Rhododendron sp. `Fashion' (azalea) growing in 10.4-liter containers were irrigated only at dawn with overhead impact sprinklers or pulse-irrigated three or four times each day with a drip system. Plant water potential was measured diurnally each week for 24 weeks, and growth was measured at the end of the growing season in December. Overhead irrigation resulted in less growth of all species than plants maintained near 100% container moisture with pulse irrigation. With the exception of photinia, more growth was associated with significantly lower daily accumulated water stress. Water stress of overhead-irrigated plants was generally not severe enough to cause stomata1 closure.

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Abdul K. Janoudi, Irvin E. Widders, and James A. Flore

Cucumber plants were cultured in a greenhouse and subjected to either well-watered or water deficit conditions that reduced leaf water potential to-0.6 MPa. Leaf gas exchange measurements were conducted using an open gas exchange system. Carbon dioxide assimilation (A) attained saturation at a photon flux density (PFD) of 1000 μmol·m-2·s-1 (400-700 nm). There were no significant differences in A at ambient temperatures between 16 and 34C. Water use efficiency decreased rapidly with increasing vapor-pressure deficits to 2.5 kPa. Water stressed plants had lower stomata1 conductances and CO2 assimilation rates. The decrease in A was only partially due to stomata1 closure. The A vs. intercellular CO (Ci) relationship for stressed leaves revealed a change in the CO, compensation point, and that nonstomatal factors were contributing to the decrease in A in stressed plants. Thus, feedback inhibition of A may have occurred through photoassimilate accumulation. The concentrations of sucrose and raffinose were higher, and the concentration of stachyose was lower in leaves of stressed than of well-watered plants.