Transport roots

Evidence was obtained recently that pesticide vapors may enter the air by still another mechanism, involving plant circulation and water loss (57). Rice plants were found to efficiently transport root-zone applied systemic carbamate insecticides via xylem flow to the leaves, eventually to the leaf surface by the processes of guttation and/or stomatal transpiration, and finally to the air by surface volatilization. Results from a model chamber showed that 4.2, 5.8, and 5.7% of the residues of carbaryl, carbofuran, and aldicarb, respectively, present in rice plants after root soaking vaporized within 10 days after treatment. The major process was evaporation of surface residues deposited by guttation fluid. 

It is clear that we must look around for another mechanism of xylem transport. Root pressure can only be a reinforcing measure, particularly in the spring, when very heavy demands are made on the xylem before the leaves have burst forth and the transpiration surface of the leaves is not yet present. This gives us our cue transport in the xylem occurs, in the main, as a result of suction from above rather than pressure from below. The precondition for this suction is transpiration. 

Figure Bl.24.16. An example of the applieation of the PIXE teelmique using the NMP in the imaging mode. The figures show images of the eross seetion tlirough a root of the Phaseolus vulgaris L. plant. In this ease the material was seetioned, freeze-dried and mounted in vaeuiim for analysis. The seales on the right of the figures indieate the eoneentrations of the elements in ppm by weight. It is elear that the transports of the elements tlirough the root are very different, not only in the eases of the major elements Ca and K, but also in the ease of the traee element Zn.

Eor pesticides to leach to groundwater, it may be necessary for preferential flow through macropores to dominate the sorption processes that control pesticide leaching to groundwater. Several studies have demonstrated that large continuous macropores exist in soil and provide pathways for rapid movement of water solutes. Increased permeabiUty, percolation, and solute transport can result from increased porosity, especially in no-tiUage systems where pore stmcture is stiU intact at the soil surface (70). Plant roots are important in creation and stabilization of soil macropores (71). 

Preferential flow through root-mediated soil pores has been demonstrated for chloride, nitrate, and other ions that are not sorbed onto soil organic matter and clays. However, pesticide sorption onto soil affects both mobiUty of the pesticide as well as its residual life in the soil. Pesticide sorption onto root organic matter or organic linings of worm burrows may also slow transport of pesticides relative to water (72), thus countering the effects of increased permeabihty caused by roots. 

After determination of the seasonal variation in alkaloidal content of the leaves, stems and roots of belladonna and the production of evidence that there is a considerable movement of alkaloid upwards from root to leaves and a small transport in the opposite direction, Cromwell found that of a laige number of amines injected, with or without glucose, into... 

The SAH water potential determines many aspects of their behavior in the soil. The processes of water redistribution in the soil, its transport to the plant roots, and assimilation follow the osmotic laws and are regulated by the thermodynamic potential. 

It is interesting to note that independent, direct calculations of the PMC transients by Ramakrishna and Rangarajan (the time-dependent generation term considered in the transport equation and solved by Laplace transformation) have yielded an analogous inverse root dependence of the PMC transient lifetime on the electrode potential.37 This shows that our simple derivation from stationary equations is sufficiently reliable. It is interesting that these authors do not discuss a lifetime maximum for their formula, such as that observed near the onset of photocurrents (Fig. 22). Their complicated formula may still contain this information for certain parameter constellations, but it is applicable only for moderate flash intensities. 

If the film is nonconductive, the ion must diffuse to the electrode surface before it can be oxidized or reduced, or electrons must diffuse (hop) through the film by self-exchange, as in regular ionomer-modified electrodes.9 Cyclic voltammograms have the characteristic shape for diffusion control, and peak currents are proportional to the square root of the scan speed, as seen for species in solution. This is illustrated in Fig. 21 (A) for [Fe(CN)6]3 /4 in polypyrrole with a pyridinium substituent at the 1-position.243 This N-substituted polypyrrole does not become conductive until potentials significantly above the formal potential of the [Fe(CN)6]3"/4 couple. In contrast, a similar polymer with a pyridinium substituent at the 3-position is conductive at this potential. The polymer can therefore mediate electron transport to and from the immobilized ions, and their voltammetry becomes characteristic of thin-layer electrochemistry [Fig. 21(B)], with sharp symmetrical peaks that increase linearly with increasing scan speed. 

Mosses and liverworts (Bryophyta) are more complex than algae. Some of the larger species have structures that superficially appear similar to roots, stems and leaves, but they lack the internal conducting systems present in the vascular plants (Tracheophyta). Internal transport systems (vascular systems) make possible the large sizes of terrestrial plants where the soil is the source of some requisites (water, mineral nutrients) and the air is the source of others (CO2, sunlight). The different groups of vascular plants are characterized primarily by their methods of reproduction. Vascular plants are the source of all wood. 

Zhang, J. Davies, W.J. (1987). Increased synthesis of ABA in partially dehydrated root tips and ABA transport from roots to leaves. Journal of Experimental Botany, 38, 2015-23. 

Macklon, A.E.S. (1975). Cortical cell fluxes and transport to the stele in excised root segments of Allium cepa L. I. Potassium, sodium and chloride. Planta, 122, 109-30. 

Pitman, M.G. Saddler, H.D. W. (1967). Active sodium and potassium transport in cells of barley roots. Proceedings of the National Academy of Sciences, USA, 57, 44-9. 

Wyse, R.E., Zamski, E. Tomos, A.D. (1986). Turgor regulation of sucrose transport in sugar beet tap root tissue. Plant Physiology, 81, 478-81. 

Apoplastic transport of sodium across the root Plant vigour (degree of dwarfing)... 

Fig. 1. Relative composition of root microsomal membranes from 24 land races, varieties and breeding lines of rice which differ in their salt resistance. Campesterol, Stigmasterol and Sitosterol as % of total sterols 16 0, 18 1, 18 2 and 18 3 fatty acids as % of total fatty acids Na transport on a relative scale from (1) lowest to (9) highest. Data of D.R. Lachno, T.J. Flowers A.R. Yeo (unpublished).

There has been considerable interest in the use of plants for bioremediation and this merits a rather extensive discussion. Plants can play an important role in bioremediation for several reasons (1) they can transport contaminants from the soil, (2) they can metabolize the contaminants after uptake, or (3) they can produce exudes that support microbial activity for degradation of the contaminants. In addition, bacteria can produce metabolites that counter the effect of toxins produced by fungi, and serve as biocontrol agents that diminish the need for the application of agrochemicals. Plant exudates play an important role in supporting the growth and activity of bacteria that carry out the degradation of contaminants in the rhizosphere and rhizoplane (the external surface of roots... 

Mammalian cytochrome P450 2E1 was introduced into tobacco plants that were exposed to trichloroethene in hydroponic medium for 5 d. Trichloroethene epoxide was produced initially, and was rearranged to trichloroacetaldehyde, which was then reduced to trichloro-ethanol. This was found in samples of leaves, stems, and roots, but was absent in the control plants. Trichloroethanol was subsequently transported to the leaves where it was apparently metabolized (Doty et al. 2000). 

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