Transport of Na and Cl across exuding tomato (Lycopersicon esculentum Mill.) roots was determined as a function of ambient NaCl concentrations in the ranges of both systems 1 and 2.Kinetics of radial transport under steady-state conditions and the effect of dinitrophenol indicate that Na and Cl were transported by two (5,16,17,19,24,30,34,37). Both the root and the stem have been implicated in the regulation of Na transport to the leaves. Basically, the proposed mechanisms of root regulation involve discriminatory exclusion of Na at the plasmalemma (10, 13, 20), Na-selective absorption into the vacuole by the tonoplast (18) and possibly, active Na extrusion from the cortical cells across the plasmalemma (1 1, 18, 28, 29, 31). Further Na dilution may occur in the stem where Na is selectively withdrawn from the xylem stream by adjacent living cells (1,16,17,30,34,36) and either sequestered there or retranslocated by way of the phloem to the root (5,23).Directly related to the mechanism of exclusion, and perhaps differing only by degree, is the mechanism whereby accumulator plants translocate Na or Cl readily to the shoots. Recently, the concept of an active anion pump as the driving force for cation transport to the xylem has received increasing support (2-4, 12, 26, 27, 35). The rationale for this theory is based primarily on the interpretation of electrochemical potentials 64 measured across exuding roots. However, the interpretations are not unequivocally accepted (18,32,33), and the mechanism of Na and Cl transport to the xylem remains in doubt.The purpose of the present investigation was to test further the active anion pump concept of salt transport with a plant that readily transports Na and Cl to the shoot. The tomato plant was chosen because it meets this criterion and because the transport of Na by this plant has been reported to be metabolically facilitated (15). The role of metabolism and steady-state kinetics of radial transport were determined over a broad range of ambient NaCl concentrations.
MATERIALS AND METHODSPlant Culture. Decapitated root systems from 23-day-old tomato (Lycopersicon esculentum Mill. cv. Heinz 1350) plants were used as the experimental material. Plants were grown from seed germinated between moist paper towels suspended over tenth-strength Hoagland's solution. Seedlings were transferred when 5 cm high to 14-liter polyethylene containers of half-strength Hoagland's solution. Phosphate was reduced to 0.25 mm and Fe was added as the metal chelate of diethylenetriamine pentaacetate. Culture solutions were prepared from demineralized water and reagent-grade salts. Eight plants per container were supported in holes in Styrofoam' covers with strips of polyurethane foam wrapped around the stem. The plants were grown in environmental chambers at 25 C and with a 16-hr photoperiod at 3300 ft-c light intensity. Solutions were aerated continuously and the pH was maintained between 6.0 and 6.5 with HNO.Experimental Procedure. All plants were transferred to 1 meq/1 CaSO4 solutions (pH 6) f...