Measurements of cell lengths made at 0.5 millimeter intervals in median longitudinal sections of the primary roots of com (Zea mays) were used to construct a growth curve. The region 1.5 to 4.0 millimeters from the apex contained the largest number of elongating cells. Absorption of "Rb* was measured using intact, dark-grown com seedlings. Following uptake and exchange, the terminal 8.0 millimeters of each root was cut into four 2.0 millimeter segments. Maximum "Rb+ uptake occurred in the region from 0.0 to 4.0 millimeter from the root tip. Washing the intact primary root in fresh 2.0 millimolar CaSO4 for 2 hours prior to uptake augmented the rate of "Rb+ uptake in all regions. Illumination with white light during washing caused a reduction of "Rb+ uptake as compared with controls washed in darkness, and the region of greatest light response was the region of elongation. Removal of the coleoptile prior to washing did not prevent the light inhibition of subsequent "Rb+ uptake. Removal of the root cap prior to washing in light partially reversed the light-induced inhibition of the washing response.The rate of absorption of mineral ions by cells in the root is influenced by the distance of the absorbing cells from the root tip (1,2,13,14). Longitudinal profiles of K/Rb absorption in corn show an absorption peak in the region of cell elongation as compared with the meristematic and early maturation zones adjacent to the elongating cells (2, 13) These highest rates of K/Rb absorption have been attributed to the involvement of those ions in growth, specifically cell enlargement (5).Another influence on ion uptake is revealed as the washing response (11,17,21): the rates of ion uptake may be augmented by washing the roots just prior to the uptake period. Although the magnitude of this response can be questioned as involving a recovery from wounding (4, 12), nevertheless, some of the published data involved intact portions of roots where injury presumably would not have been involved (1 1). It has been suggested that this washing response involves some native growth factor or inhibitor (11, 21), but there is not presently any conclusive experimental support for this, nor has any identity for such an agent been suggested.The present study reveals that there is yet a third influence: light. Light is already known to inhibit root growth (15,23,30), and it is shown here that it also has an inhibiting effect on the washing response as well. Furthermore, the data preFlorida Agricultural Experiment Station Journal Series No. 7467. sented show that the maximal inhibiting effect of light occurs in the same region which shows maximal elongation, maximal ion absorption, and maximal washing response.
MATERIALS AND METHODS Plant MaterialCorn seedlings (Zea mays L.) of two different cultivars ('XL-80,' DeKalb; 'Merit,' Asgrow) were used in these experiments. One-hundred gram lots of dry seeds were washed, surface-sterilized, and incubated in distilled water at 30°C in the dark as described earlier (21). The flask was place...