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A fluorimetric ratio technique was elaborated to measure apoplastic pH in the outer root cortex of maize (Zea mays L.) grown hydroponically. A newly synthesized fluorescent probe, fluorescein boronic acid (pK(a) = 5.48), which covalently binds to the cell wall of the outer cell layers, was used. Under conditions of saturating ion concentrations the apoplastic pH was determined along the root axis ranging from 1 to 30 mm behind the root tip. Apoplastic pH was recorded for root segment areas (1 mm(2)), and pH values of high statistical significance were obtained. With an external solution of pH 5, the apoplastic pH was about pH 5.1 in the division zone, between pH 4.8 and 4.9 in the elongation region and about pH 4.9 in the root hair zone. At an external pH of 8.6, the difference between the external pH and the apoplastic pH was considerably more, with a pH of 5.2-5.3 in all root zones. Addition of 1 mM NH(4)(+) caused a small apoplastic pH decrease (0.05 of a pH unit) in all root zones. Apoplastic alkalization upon application of 6 mM NO(3)(-) was highest (0.3 of a pH unit) in the zone where root hairs emerge; in the division and early elongation zones, apoplastic pH increased only transiently. In the presence of 10 mM HCO(3)(-), NO(3)(-) elicited a higher and persistent alkalization (0.06-0.25 of a pH unit) in all root zones. Application of fusicoccin reduced apoplastic pH from 4.85 to 4.75 in the elongation zone, while inhibition of the H(+)-ATPase with vanadate alkalized the apoplast in the root hair zone from pH 5.4 to 5.6. The observed pH differences along the root axis upon differential N supply and application of HCO(3)(-) provide evidence that this new pH technique is a useful tool with which to measure apoplastic pH, and in future may permit measurements at microsites at the cell level by use of microscope imaging.

1989. Effect of acidic fog on needle surface and water relations of Picea abies. -Physiol. Plant. 75: 201-207.Young spruce trees [Picea abies (L.) Karst.] exposed to acidic fog (pH 3) showed a disintegration of the epicuticular waxes of the current year's needles as compared with trees treated with a fog of pH 5. The fog treatment was followed by a period in which the trees received different water supply. Under water stress conditions, trees that had been exposed to the acidic fog showed significantly higher transpiration rates than control trees that were treated with a fog of pH 5. The water loss of the controls was 0 at the middle of the photoperiod, while the trees pretreated with acidic fog still showed a substantial transpiration rate at this time. Water loss of excised twigs measured in the dry atmosphere of a desiccator also provided evidence that the water holding capacity of needles pretreated with acidic fog was affected. There is evidence that particularly the cuticular transpiration was increased by pretreatment with acidic fog. The xylem water potential of twigs pretreated with acidic fog was significantly lower than that of twigs pretreated with a fog of pH 5, while the osmotic potential was not affected by the different fog treatments. It is suggested that in draught years trees with a damaged cuticle caused by acidic fog will be affected in their resistance against water stress. In this way acidic fog could be involved in forest decline now widely spread in Central Europe.

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