Physicochemical factors affecting the uptake by roots and translocation to shoots of amine bases in barley

The uptake by barley roots from nutrient solution and subsequent transport to shoots of two series of amine bases were measured over 6 to 72 h. The compounds were chosen to span systematically ranges of lipophilicity (assessed using 1-octanol/water partition coefficients, K_ow) and pKa that would include commercial pesticide amines. In a series of six substituted phenethyl amines, strong bases with pKa∽9·5, all the compounds were strongly taken up by roots from solutions of pH 8·0; uptake declined substantially as the pH was lowered to 5·0, especially for the compounds of intermediate lipophilicity (log K_ow 2 to 3). This uptake could be ascribed to three processes: (i) accumulation of the cation inside the root cells due to the negative charge on the plasmalemma, as given by the Nernst equation and important only for the polar compounds which have low permeation rates through membranes; (ii) accumulation into the vacuole by ion-trapping, which was the dominant process at high pH for all compounds and at all pH values for the compounds of intermediate lipophilicity; (iii) partitioning on to the root solids, substantial only for the most lipophilic compounds. Translocation to shoots was proportional to uptake by roots, this ratio being independent of external pH for each compound and being optimal for the compounds of intermediate lipophilicity. Such proportionality was also observed in a series of three weaker bases of intermediate lipophilicity, in which compounds of pKa 7·4 to 8·0 were also well taken up and translocated whereas the very weak base 4-ethylaniline (pKa 5·03) was much less so. Tests with quaternised pyridines confirmed that organic cations move only slowly through membranes. The observed behaviour of the amines could be modelled reasonably well assuming that transport within the plant was dominated by movement across membranes of the non-ionised species, and this appeared to be true even for the most lipophilic phenethylamine (log K_ow 4·67) studied, though its long-distance movement would be as the protonated species. © 1998 Society of Chemical Industry     

Relationships between lipophilicity and the distribution of non-ionised chemicals in barley shoots following uptake by the roots

Determinations were made of the distribution of two series of non-ionised chemicals, ^O-methylcarbamoyloximes and substituted phenylureas, in barley shoots, following uptake by the roots from solution. The concentrations in basal and central shoot sections became constant after 24 to 48 h for all but the most lipophilic chemical studied, and were then greatest for the more lipophilic chemicals. Amounts in the leaves generally increased up to 72 or 96 h, when degradation balanced translocation. The accumulation of chemical in the lower section of shoots can be ascribed to a partitioning process similar to that in roots, the chemical being partitioned between the shoot and the xylem transpiration stream; this uptake could be estimated from the octan-1-01/water distribution coefficients, and was predicted to be greatest for compounds for which log K_ow=4. 5.     

Uptake of systemic fungicides by maize roots

The absorption of nine benzimidazole derivatives and four thiophanates by excised maize roots was shown to be due to passive mechanisms because a. the temperature coefficient was low, b. anaerobic conditions or metabolic inhibitors had little or no effect, c. the rate of uptake was a linear function of external concentration, d. compounds of similar structure did not compete for absorption.For benzimidazole derivatives, we observed a very rapid initial uptake which reached a maximum after one or two hours; this saturation did not occur with thiophanates.The effect of pH on the root absorption of benzimidazole derivative indicates that molecular (or unionized) forms of these amphoteric compounds were taken up preferentially; the behaviour of thiophanates was different.As observed with other pesticides, root absorption was greater for lipophilic than for lipophobic substances and in our experiments the rate of uptake of fungicides was well correlated to their partition coefficient in an octanol/ water system at pH 6.5.Generally, the various fungicides were taken up to the same extent all along the length of the roots.     

Genetic correlations in resistance to morpholine and piperidine fungicides inPyrenophora teres populations

Highly significant genetic variation (P<0.001) in resistance to the morpholine fungicides fenpropimorph, tridemorph and dodemorph and the piperidine fungicide, fenpropidin was found in different populations ofPyrenophore teres in North America and Europe which had not been previously exposed to these fungicides. Resistance phenotypes were continuously distributed for each fungicide in each population. Cross resistance relationships were determined by estimating genetic correlation coefficients in resistance to all pairwise combinations of fungicides. The majority of the correlation coefficients were highly positive for all fungicide combinations in all populations; eight of 36 (22%) coefficients were not significantly different from 1 (P>0.05). This result is consistent with the hypothesis that many of the same genes, or genes in gametic disequilibrium, control resistance to more than one fungicide in most populations ofP. teres and that these fungicides comprise a single cross resistance group. Three of 36 (8%) correlation coefficients were not significantly different from 0 (P>0.05) indicating that, in these populations, independent genes controlled resistance to these fungicides. The results of this study indicate that although most of the same genes control resistance to morpholine and piperidine fungicides inP. teres, differences in frequencies of these genes among populations can result in different cross resistance relationships from one population to another.     

Transport via xylem of atrazine, 2,4-dinitrotoluene, and 1,2,3-trichlorobenzene in tomato and wheat seedlings

Transport of atrazine (ATR), 2,4-dinitrotoluene (DNT), and 1,2,3-trichlorobenzene (TCB) from roots to shoots via xylem of wheat and tomato seedlings was measured following a 24-h exposure of plant roots to hydroponic solutions of these organic compounds. Transport of the compounds from roots to shoots reached equilibrium within 24 h, consistent with an earlier finding. Low concentrations of TCB were detected in the final external solution and the xylem efflux of control wheat seedlings. This suggested that there was a fast foliar uptake of TCB and its downward movement via phloem of the wheat seedlings. Concentrations of DNT, ATR, and TCB in xylem effluxes of wheat and tomato increased significantly with increases of their external concentrations. The translocation stream concentration factors (TSCF), i.e., the ratios of the concentrations in xylem sap to those in external solution, of the compounds with tomato seedlings followed the order of ATR > DNT >> TCB, which was inversely correlated with the log K_ow (the octanol–water partition coefficient) of the compounds. The observed xylem transports of DNT and TCB from roots to shoots with wheat seedlings were lower than those with tomato seedlings. ATR exhibited a high xylem transport with the two plant species, which resulted presumably from an atrazine–metal complex formation.     

Relationships between lipophilicity and root uptake and translocation of non-ionised chemicals by barley

The uptake by roots from solution, and subsequent translocation to shoots in barley, of two series of non-ionised chemicals, O-methylcarbamoyloximes and substituted phenylureas, were measured, Uptake of the chemicals by roots was greater the more lipophilic the chemical, and fell to a lower limiting value for polar chemicals. Translocation to the shoots was a passive process, and was most efficient for compounds of intermediate polarity. Both processes had reached equilibrium within 24h of treatment. The reported behaviour of many pesticides in various plant species agrees with the derived relationships, but the detailed mechanisms of these processes are unknown.     

Uptake and translocation of non-ionised pesticides in the emergent aquatic plant parrot feather Myriophyllum aquaticum

The uptake of four (14)C-labelled non-ionised compounds, the methyl carbamoyloxime insecticide/nematicide oxamyl and three model phenylureas, from solution by rooted stems of the aquatic plant parrot feather [Myriophyllum aquaticum (Vell.) Verdc], together with translocation to the emergent shoots, was measured over periods of 24 and 48 h. Uptake into the submerged tissues of roots and stem base could be ascribed to two processes: movement into the aqueous phase of cells and then partitioning onto the plant solids. This latter process was related to lipophilicity (as measured by the l-octanol/water partition coefficient, K(ow)) and gave rise to high uptake rates of the most lipophilic compounds. Translocation to shoots was passive and was optimal at log K(ow) approximately 1.8, at which the efficiency of translocation of compound was about 40% of that of water. This optimum log K(ow) was identical to that observed previously in barley, although the translocation efficiency was somewhat less in parrot feather. Solvation parameters were applied to model uptake and translocation of a set of ten compounds by barley with the particular objective of understanding why translocation efficiency is lower at log K(ow) > 1.8.     

Effects of sterol biosynthesis-inhibiting fungicides and plant growth regulators on the sterol composition of barley plants

A number of sterol biosynthesis-inhibiting (SBI) fungicides and plant growth regulator analogs were applied as root drenches to barley seedlings and their effect on the total sterol composition of the roots and shoots was measured by gas-liquid chromatography. Prochloraz was found to be inactive in this system, probably because of poor uptake, while the other compounds could be divided into two groups according to their mode of action as assessed by sterol profiling. The morpholines tridemorph and fenpropimorph inhibited the enzyme cycloeucalenol—obtusifoliol isomerase whereas triadimenol, nuarimol, paclobutrazol, and triapenthenol (RSW 0411) inhibited the enzyme responsible for the removal of the C-14 methyl group. Effects of individual diastereo-isomers and enantiomers of some compounds on sterol profiles were compared with their known fungicidal and anti-gibberellin properties. Shoot growth was reduced by all the compounds tested, paclobutrazol, nuarimol, and triapenthenol being the most effective. As well as inducing accumulation of abnormal sterols, SBI fungicide treatment changed the ratio of campesterol to stigmasterol and sitosterol. It is hypothesized that this may reflect changes in membrane architecture and may offer an explanation for the increased frost hardiness sometimes observed with SBI fungicide-treated plants.     

Root Uptake and Xylem Translocation of Pesticides from Different Chemical Classes

A pressure-chamber technique was used to study the root uptake and xylem translocation of some fungicides, herbicides and an insecticide from different chemical classes in detopped soybean roots. Physiological parameters such as K⁺ leakage from roots, K⁺ concentrations in the xylem sap, and protein and ATP levels in the root cells were measured so as to evaluate any potential damage of this technique to the root system. HPLC was used to quantify the compounds in the xylem sap. The pressure-chamber technique has proved useful to study the root uptake and translocation of pesticides, does not damage the root system, and allows one to obtain appreciable volumes of xylem sap that can be analysed directly by HPLC, thus avoiding dependence on the availability of radio-labelled compounds. The concentration of each pesticide in the xylem sap showed a steady-state kinetic profile. Non-linear regression analysis was used to calculate the steady-state concentration and the time required to achieve 50% of the steady-state concentration (TSSC₅₀). TSSC₅₀ was well correlated with log K_ow; the more lipophilic the compound the more time was required to reach the steady-state concentration. The efficiency of translocation was assessed by the transpiration stream concentration factor (TSCF) and a non-linear relationship between TSCF and log K_ow was observed. The highest TSCF values were measured for those compounds with log K_ow values around 3, a lipophilicity value similar to that reported earlier in an analogous experiment with detopped soybean plants but slightly higher than that reported in earlier experiments with intact barley plants. Lower TSCF values were obtained with chemicals with log K_ow values below as well as above 3. © 1997 SCI.     

Uptake and translocation of some pesticides by hypocotyls of radish seedlings

Some of the factors affecting absorption and translocation of pesticides by the hypocotyls of intact radish (Raphanus sativus, L., cv. Black Spanish) seedlings have been studied, particular attention being given to the triazine herbicides simazine, atrazine and atraton. Uptake and translocation appear to be largely passive processes and by contrast with foliar absorption seem to be unaffected by humidity, con-centration, light and by the aqueous solubilities of the compounds. Diffusion across the tissues of the hypocotyl, rather than rate of transpiration, appears to determine the rate at which atrazine and simazine are translocated to the cotyledons. For several pesticides there is a qualitative relationship between the percentages of the compounds translocated to the upper portion of the shoots and their partition coefficients in oil/water systems. In conclusion, some consideration is given to the relative importance of uptake by roots and shoots under field conditions.     

Measurement of xylem translocation of weak electrolytes with the pressure chamber technique

Xylem translocation and root uptake of weak electrolytes were investigated with the pressure chamber technique (PCT) using de-topped soybean plants. Two compounds were organic bases (fenpropimorph and imazalil) and four were organic acids (bentazone, primisulfuron-methyl, rimsulfuron and triasulfuron). The compounds covered a wide range of log KOW and pKa values. Concentrations in external solution and in xylem sap were measured by HPLC at pH values in external solution of 4.5, 6.5 and 8.5. For weak bases, translocation was higher at low pH and the transpiration stream concentration factors (TSCF) were in the range 0.31-0.95. At pH 8.5, the concentrations in leaking xylem sap were very low for fenpropimorph, and steady-state was probably not reached. For weak acids, TSCF values derived with external pH from 4.5 to 8.5 were in the range 0.55-1.50 for primisulfuron-methyl, 0.64-1.35 for rimsulfuron, 0.81-0.93 for triasulfuron and 0.69-0.92 for bentazone. The variation of TSCF of the weak electrolytes was much smaller in these PCT experiments than in recent experiments with intact plants. The likely reason is that de-topped soybean plants in the pressure chamber seemed to be unable to regulate their xylem sap pH, which was almost identical to the pH in external solution. Without pH differences, the ion-trap process, which is responsible for accumulation or exclusion of weak acids and bases in the xylem of living plants, does not take place. Model simulations carried out for intact and de-topped plants supported this hypothesis. By variation of the pH of the xylem sap, good agreement between measurements and simulations could be achieved.     

Modelling uptake into roots and subsequent translocation of neutral and ionisable organic compounds

A study on uptake of neutral and dissociating organic compounds from soil solution into roots, and their subsequent translocation, was undertaken using model simulations. The model approach combines the processes of lipophilic sorption, electrochemical interactions, ion trap, advection in xylem and dilution by growth. It needs as input data, apart from plant properties, log K_OW, pK_a and the valency number of the compound, and pH and chemical concentration in the soil solution. Equilibrium and dynamic (steady‐state) models were tested against measured data from several authors, including non‐electrolytes as well as weakly acidic and weakly basic compounds. Deviations from the measured values led to further development of the model approach: sorption in the central cylinder may explain the small transpiration stream concentration factor of lipophilic compounds. For non‐electrolytes, the model predicted uptake and translocation with high accuracy. For acids and bases, the tendency of the results was satisfactory. The dynamic model and the equilibrium approach gave similar results for the root concentration factor. The calculation of the transpiration stream concentration factor was more accurate with the dynamic model, but still gave deviations up to factor of ten or more. The dominating process for monovalent weak electrolytes was found to be the ion trap effect. © 2000 Society of Chemical Industry     

Physico-chemical factors affecting uptake by roots and translocation to shoots of weak acids in barley

The uptake from solution of maleic hydrazide, flamprop and a series of phenoxyacetic acids by roots, and their subsequent translocation to shoots, was measured in barley. Both uptake and translocation increased as the pH of the solution decreased, the magnitude of the change varying amongst the chemicals tested. Uptake by roots could be accounted for by the ion-trap mechanism, which assumes that entry of the chemicals occurs largely by passive diffusion of the undissociated form of the acids, with passage of the anions across the cell membranes being very slow. The ratio of the permeability of the cell membranes to the undissociated and dissociated forms of the acids was estimated from the accumulation in roots, and in the phenoxyacetic acid series this ratio was maximal (4×10⁵) for compounds of intermediate lipophilicity. Maleic hydrazide and flamprop had much lower ratios, 1.8×10² and 10³ respectively; the value for flamprop was much less than for phenoxyacetic acids of similar lipophilicity, such as 2, 4- dichlorophenoxyacetic acid, indicating that lipophilicity may not be the sole factor determining the behaviour of weak acids in plants. Translocation to shoots was approximately proportional to the chemical concentrations in the roots.     

The metabolic fate of tridemorph in rats

A single oral dose of [¹⁴C]tridemorph was partly, but rapidly absorbed by rats. Most of the radioactivity was excreted with a half-life of about 15 h. During 5 days, 42.6% was excreted in the urine, 46.7% in the faeces, 1.5% in the expired air and 3.4 % was still retained. 24 % was excreted in the 48 h bile. Sequential wholebody autoradiography indicated that much of the radioactivity was confined to the gastrointestinal tract, liver and kidneys. There was no unexpected uptake of radioactivity. Urinary metabolites were more polar than tridemorph and were also detected in the bile and faeces. The major metabolite in 24 h urine, accounting for 22.3% of the dose appeared to be a side-chain hydroxylated derivative. Cleavage of the morpholine ring was limited to about 1.5 % of the dose.     

Resistance to fungicides which inhibit ergosterol biosynthesis in laboratory strains of Botrytis cinerea and Ustilago maydis

The strains of Botrytis cinerea or Ustilago maydis selected on fenarimol, triarimol, or triadimefon were also resistant to the other inhibitors of sterol C-14 demethylation; the sterol composition of the strains was normal. Among the isolates of U. maydis resistant to dodemorph, fenpropidin, fenpropimorph and tridemorph, some were resistant to the 15-azasteroid A 25822B and did not contain ergosterol. The other strains remained sensitive to A 25822B and had a normal sterol composition. All the resistant isolates and the wild-type were inhibited to the same extent by nystatin and pimaricin.     

Phloem translocation of strong acids—glyphosate,substituted phosphonic and sulfonic acids—in Ricinus communis L

The mobility in phloem of several substituted phosphonic acids and a sulfonic acid was studied in the castor bean plant, Ricinus communis L. For a series of¹⁴C-labelled phosphonate mono-esters applied to the petioles of mature leaves, phloem transport was modest, becoming poor over longer distances in the plant. Substituted phenylphosphonic acids were more efficiently moved in phloem; uptake from the petiole and subsequent redistribution were slow, but these dibasic compounds were very stable in plants and substantial amounts reached the roots after 72 to 120 h. Glyphosate was very efficiently transported to phloem sinks even within 24 h, with high concentrations in phloem sap. Toluene-4-sulfonic acid moved predominantly in the xylem to the mature leaves and its phloem transport was poor. Transport patterns are considered in relation to the physico-chemical properties of the compounds. Ion trapping appears to play little part in the phloem transport of these strong acids, though the good accumulation and transport in phloem of the complex molecule glyphosate cannot at present be explained.     

Genetics of responses to morpholine-type fungicides and of avirulences inErysiphe graminis f. sp.hordei

The genetics of the responses of the barley powdery mildew pathogen,Erysiphe graminis f.sp.hordei, to three morpholine-type fungicides were studied. Resistances to a phenylpropylamine fungicide, fenpropidin, and to a morpholine, fenpropimorph, co-segregated in crosses of a sensitive isolate, DH14, with each of two resistant ones, CC151 and CC152. In the cross CC151×DH14, the results were consistent with resistance to both fungicides being controlled by a single gene, at a locus namedFenl. In the other cross, CC152×DH14, the genetics of resistance were more complicated; the data were consistent with the segregation of two complementary, unlinked genes which each conferred resistance to both fungicides. Fenpropidin-resistant progeny of CC151×DH14 were significantly more resistant to fenpropimorph than were fenpropidin-resistant progeny of CCI 52×DH14, although the resistant progeny of the two crosses did not differ significantly in their level of fenpropidin resistance. Fenpropidin-resistant progeny of CC151×DH14 were significantly more resistant to another morpholine, tridemorph, than were fenpropidin-sensitive progeny, but this was not the case for CC152×DH14. Resistance to triadimenol, a C14 demethylation-inhibitor (DMI) fungicide, segregated in both crosses. Triadimenol resistance appeared to be controlled by one gene in each cross and was not associated with morpholine resistance. CC151×DH14 also segregated for eight avirulence genes. Two of these matched theMla6 resistance, while one gene matched a previously unknown resistance in a Pallas near-isogenic line, P17, which also carries a known resistance gene,Mlk. Fenl was not significantly linked to the triadimenol resistance gene,Tdl(a), or to any of the eight avirulence genes.Avr _a6 1, Avr _a12 ,Avr _La ,Avr _p17 andTdl(a) were linked, as wereAvr _a 10 andAvr _k .Abbreviations ED₅₀ median effective dose - Fpd fenpropidin - Fpm fenpropimorph - PCA principal components analysis - Tdm tridemorph     

Effects of some fungicides on Rhizobium trifolii and its symbiotic relationship with white clover

A comparison has been made of the effects of some protective and systemic fungicides, and an eradicant fungicide, on the growth, metabolic activity and nitrogen-fixing capacity of Rhizobium trifolii. Effects on the bacterium grown in vitro with a combined nitrogen source were not necessarily reflected in the nitrogen-fixing capacity of excised nodulated roots of white clover. Symbiotic nitrogen fixation was affected by thiram, oxycarboxin and “Ethylan CP”, but was unchanged by benomyl, captan, carbendazim, carboxin, dodine, dimethirimol, ethirimol, tridemorph, triforine or thiophanate-methyl. None of the fungicides tested altered the leghaemoglobin content of the root nodules.     

Comparative systemic translocation of several xenobiotics and sucrose

The systemic movement of several xenobiotics was compared in soybean and barley. The more symplastic compounds were also compared to the movement of sucrose. The uptake and efflux from potato tuber tissue was studied and related to the in vivo translocation patterns. The patterns of translocation ranged from primarily apoplastic to ambimobile to symplastic. When the percentage of xenobiotic available for translocation was evaluated there were major differences in patterns of translocation, between plant genera. In barley fenapanil, fenarimol, and oxamyl exhibited primarily apoplastic transport while all three were more ambimobile in soybean. Basipetal transport of oxamyl was 4.2% in barley compared to 30.8% in soybean. Basipetal translocation of benomyl remained very low at 3.0 and 4.1% in barley and soybean, respectively, while sucrose was about 60% in both species. Glyphosate and sucrose were translocated in a similar pattern. The transport of 2,4-D was primarily symplastic, however, retention in the tissue appeared to limit the rate of movement when compared to sucrose. Uptake and efflux of fenapanil, fenarimol, and 2,4-D illustrated the possible role that cellular binding or partitioning may play in systemic translocation. In conjunction with the uptake and efflux, and systemic movement in plants, the octanol/water partition coefficients, log P, for fenarimol and fenapanil, 0.67 and ?0.03, respectively, are correlated with the possible role of cellular binding or partitioning in the systemic movement of xenobiotics.