A computer-controlled multichannel data acquisition system was employed to obtain continuous measurements of net nitrate or chlorate uptake by roots of intact barley plants (Hordeum vulgare cv Betzes) using nitrate-specific electrodes. Plants, previously grown in solutions maintained at 10 or 200 micromolar N03-(low N or Rates of uptake of the major inorganic nutrients, by roots of higher plants, are extremely sensitive to the availability of these nutrients in the ambient solution. Generally, the capacity for uptake increases with low availability so that internal concentrations tend to be maintained at prescribed levels (2, 13). Such responses have been interpreted to reflect the operation of regulatory mechanisms which may function via negative feedback effects upon the transport systems involved (3,4,11,19,23 (14) demonstrated that NO3-'influx' was reduced and NO3-efflux enhanced by prior growth of wheat seedlings at increasing levels of NO3-(0.25 to 15 mM). However, the term influx in these studies referred to rates of '5NO3 uptake based upon exposures ranging from 0.5 to 6 h. Unfortunately, if the half-life for cytoplasmic exchange is short by comparison to the uptake period, then the measured flux would approximate net uptake rather than unidirectional influx. In these experiments, NO3 efflux increased as the nitrate concentration of the growth medium was increased from 1.0 to 15 mm. Here also, the long term basis ofthe flux measurements (20.5 h) would inevitably lead to an underestimate ofefflux if t1/2for cytoplasmic exchange is short by comparison to flux measurements. Our recently reported estimate of cytoplasmic half-life for NO3 exchange in barley roots (7) suggest that this is indeed the case; t/2 was estimated to be 17 min. Nevertheless, the former study as well as earlier and more recent work from the same laboratory (16-18) attest to the potential importance of efflux in determining net uptake rates.Recently, two techniques which facilitate the measurement of nitrate fluxes over relatively short time periods (610 min) have been reported from this laboratory. First, 36C103-has been demonstrated to be a tracer for nitrate (7). Second, a microcomputer-based system has been described (12) which permits rapid and automatic measurement of ion uptake, using ion-specific electrodes. The frequency with which measurements can be obtained by the latter method leads to extremely sensitive estimates of uptake even in experiments of short duration (5-10 min). The present work was undertaken, using these methods, to explore the relationships between nitrogen status and NO3 flux into barley roots.
MATERIALS AND METHODSPlant Culture. Barley plants (Hordeum vulgare L. cv Betzes or Bonanza) were grown hydroponically, in 36-L tanks containing 0.01x Johnson's modified inorganic medium in which NO3 was maintained at 10 gM (low N) or 200 gM (high N) as described in a previous communication (6). Tanks were contained in a Conviron growth cabinet at 26°C and 70% RH and illumination was provided by fluorescent l...