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An electron microprobe (EMP) analysis of silica (SiO,) deposition in the epidermis of developing internodes of the perennial scouring rush (Equisetum hyemale var. affine) indicates that SiO, is first detected in the stomata1 apparatus beginning with internode 3, then the epidermal papillae (internode 8), and finally in radial cell walls of the long epidermal cells (internode 10). This process is initiated in the intercalary growth regions at the bases of the elongating internodes. The deposition of SiO, in long epidermal cell walls occurs after internodal extension has ceased and should therefore be considered as one of the final stages in internodal differentiation that involves strengthening the cellulosic framework of the cell wall. EMP measurements indicate that SiO, in stomata is equivalent to 30% of a pure SiO, standard and that SiO, in the radial walls of long epidermal cells averages twice that measured on the tangential walls of these same cells. This study supports the view that silicification plays a major role in strengthening the developing perennial scouring rush internodal system and that regulation of this process in this and other species of Eguisetum, whose SiO 2 deposition patterns are markedly different, deserves further study.

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Using scanning electron microscopy, we determined the kinds and distribution of epidermal cell types in Avella inflorescence bracts (glume, lemma, and palea). Electron microprobe analysis of silica deposition in these epidermal cells showed that silica cells constitute one of the important deposition sites. Probe ratio data indicate that the silica deposited is 74 % pure. Significant amounts of silica also become deposited in the trichomes and lesser amounts in the walls of long epidermal cells. None could be detected in the stomata. The possible functional significance of silica deposition in epidermal cells of these bracts is discussed.

The random cell movement of BALB/c 3T3 and SV40 virus-transformed BALB/c 3T3 cells within homogeneous aggregates was studied by observing the degree of penetration of newly attached [aH]thymidine-labeled cells into the interior of the aggregates. The 3T3 cells penetrated into 3T3 aggregates an average of 0.89 cell diameter in 1.5 days, whereas the SV40-3T3 cells penetrated into SV40-3T3 aggregates an average of 3.20 cell diameters in the same time. Treatment of the aggregates with theophylline, theophylline plus prostaglandin E,, or theophylline plus dibutyryl cyclic AMP all decreased the penetration of the SV40-3T3 cells into SV40-3T3 aggregates (2.36, 1.22, and 0.79 cell diameters, respectively). The same treatments had little effect on 3T3 aggregates.The ultrastructure of 3T3 and SV40-3T3 cells in aggregates was examined by transmission electron microscopy. The 3T3 cells in aggregates were surrounded by microvilli and lamellipodia which were in contact with neighboring cells, whereas SV40-3T3 cells were nearly devoid of microviUi and lamellipodia and made contact at broader, less regular surface undulations. Treatment with theophylline plus dibutyryl cyclic AMP resulted in the appearance of microvilli on SV40-3T3 cells and also appeared to increase the area of intercellular contacts in both 3T3 and SV40-3T3 cells. These observations were supported for the surface cells of the aggregates by scanning electron microscopy.The increased mobility of SV40-transformed 3T3 cells relative to their nontransformed counterparts has been demonstrated in monolayer culture (8) and postulated to be a general property of transformed cells (25). Previous work from our laboratory (9) has indicated that the ability of BALB/c 3T3 cells to penetrate into aggregates or masses of the same cell type was much less than that of SVT-2 cells, an SV40 virus-transformant of the BALB/ c 3T3 line.Cyclic AMP, some of its analogues, and agents that increase cycli~ AMP levels appear to increase cell-dish adhesiveness (11,12,22) by decreased detachability. In addition, dibutyryl cyclic AMP (dbcAMP) or prostaglandin E1 (PGE1) decrease the mobility of L-929 fibroblasts in monolayer cultures (13). Since cells in tissues move over the surfaces of other cells, rather than over artificial surfaces, we thought that it was important to examine the effects of these agents on mobility in an 424