Morphological and Physiological Effects of Maleic Hydrazide on Tobacco

Tobacco plants (Nicotiana tabacum cv. Burley 21) were cultured in the greenhouse to the 18-leaf stage. The apical meristem was removed and subsequent axillary bud growth was removed by hand (controls) or axillary bud development was inhibited by application of maleic hydrazide. Compared with the controls, maleic hydrazide treated plants had a decreased stem diameter and stem weight, but an increased leaf weight and leaf weight/area. Plant height and leaf area were the same for both treatments. Maleic hydrazide inhibited translocation of ¹⁴C from a single leaf exposed to ¹⁴CO₂. Respiration was greater than in the controls three days after application of maleic hydrazide, but 9 and 14 days after application there were no differences in respiration between the two treatments. Maleic hydrazide did not affect photosynthetic activity.     

Uptake, Cellular Distribution, and Metabolism of 14C-picloram by Excised Plant Tissues

Excised soybean (Glycine max (L.) Merr.) hypocotyls, barley (Hordeum vulgare L.) coleoptiles, barley leaf sections, and Canada thistle (Cirsium arvense (L.) Scop.) leaf discs continuously absorbed ¹⁴C-picloram from a buffered solution over a 24 h period. After an 8 h uptake period excised sections released up to 30 % of the absorbed picloram into ‘clean’ buffer solution in a 4 h period. Leaf sections released less than did the other tissues. Uptake of ¹⁴C-picloram by soybean hypocotyl and barley coleoptile sections increased with an increase in temperature from 5 to 35°C. Uptake was promoted by added ATP and sucrose but inhibited by actinomycin D, cycloheximide, and DNP. After differential centrifugation of aqueous extracts of ¹⁴C-picloram-treated excised tissues more than 95 % of the radioactivity was in the soluble fraction. In excised barley and Canada thistle leaf tissues, 3 days after treatment, part of the ¹⁴C-picloram was conjugated with plant constituents, largely with sugar(s). After acid hydrolysis of ethanol extracts of such tissues only unaltered picloram was detected. In barley coleoptile and soybean hypocotyl sections no conjugation products of ¹⁴C-picloram were detected.     

Investigations on the causes of low susceptibility of scentless mayweed to 2,4-D

White mustard (Sinapis alba L.) plants, susceptible to 2,4-D, and scentless mayweed (Tripleurospermum maritimum L.) plants, resistant to 2,4-D, markedly differ in the distribution and metabolism of 2,4-D. When 2,4-D-¹⁴C was applied onto the leaf, radioactivity was found in mustard after 8 days in the entire plant, whereas in scentless mayweed radioactivity occurred mainly in the leaf onto which it was applied and in another one or two leaves, with the roots showing only traces of radioactivity. The two plant species differed both in the character and in the number and amount of metabolites detected in aqueous and ether fractions. The metabolite with R_f 0.63 -0.65, soluble in ethylether (39% of the total radioactivity applied), and that with R_f 0.35 -0.36 (23% of the total radioactivity) were present exclusively in the roots of scentless mayweed plants. The R_f values established indicate that the former metabolite may be a conjugate with the amino acids alanine and valine and the latter a hydroxylated derivate of 2,4-D. In the shoots of both plants, 2,4-D-¹⁴C was metabolized to identical metabolites with R_f 0.59 -0.61, which occurred in mustard plants only in trace amounts. Free 2,4-D-¹⁴C occurred in the shoots of both plants and in considerable amounts also in mustard roots; it could not be demonstrated in the roots of scentless mayweed. The two species did not differ in the uptake rate or in the amount of absorbed 2,4-D-¹⁴C.     

Estimation of mutagenicity and metabolic activation after recurrent exposures ofnicotiana tabacum L. var.xanthi to 14 pesticides

Recurrent application (17 administrations in 38 days) of 14 pesticides (Karathane FN 57, Fundazol 50 WP, Dithane M 45, Topsin M 70 WP, Perozin 75 B, Fademorf EK 20, Novozir MN 80, Metation E 50, Pirimor DP, Decemtion EK 20, Zeazin 50 DP, Fatex EK 80, maleic hydrazide and Ethrel) did not increase (with the exception of maleic hydrazide) the frequency of somatic mutations in a heterozygous chlorophyll mutant ofNicotiana tabacumL. var.xanthi n. c. None of the four tested pesticides (Fademorf EK 20, Decemtion EK 20, maleic hydrazide and Ethrel) were transformed in tobacco plants to a stable mutagenic or promutagenic product active in theSalmonella (Ames) mutagenicity assay.     

The relationship between the entry of isoproturon into Alopecurus myosuroides and its effect on growth and CO2 fixation

Alopecurus myosuroides (blackgrass) was grown in nutrient and with isoproturon added to the solution when plants had three leaves. The transpiration stream coefficient factor was calculated over a period of 96h after treatment to be approximately 1. On this basis isoproturon entry into A. myosuroides was estimated using data for water loss through plants and there was a linear relationship between herbicide entry and plant weight 14 days after treatment. Treatment for at least 7 days with isoproturon at a dose of 1 μg a.i./15 ml nutrient solution (≡ 0.32 × 10^-6M) before returning plants to fresh nutrient was necessary for damage to be still evident after 14 days. This time period corresponded with the reduction of CO₂ exchange to zero as measured by infra-red gas analysis. Some recovery occurred from 6 h treatment with 120 μg a.i. isoproturon/15 ml nutrient solution when assessed after returning plants to untreated nutrient for 14 days. A quicker depletion in CO₂ uptake by blackgrass occurred when both the primary and secondary roots were treated compared with secondary alone but eventually the levels reached were similar. The ‘CALF’ model predicted much higher concentrations of isoproturon than appeared necessary to damage A. myosuroides. This suggests a major influence of climate on the plant and this and other interactions are discussed.     

Nitrogen fixation by white clover when competing with grasses at moderately low temperatures

It was the aim of this study to determine the way in which low temperature modifies the effect of a competing grass on nitrogen fixation of a forage legume. White clover (Trifolium repens L.) was grown in monoculture or in different planting ratios with timothy (Phleum pratense L.) or perennial ryegress (Lolium perenne L.) in growth chambers at either 7.5/5°C (LoT) or 15/10°C (HiT) average day/night temperatures, and with 2.5 or 7.5 mM ¹⁵N-labelled nitrate in the nutrient solution.Competition with grass led to a marked increase in the proportion of clover nitrogen derived from symbiosis (% N_sym). This increase was slower at LoT where % N_sym was reduced considerably; it was closely related to the reduction in the amount of available nitrate as a result of its being utilized by the grass.Nitrogen concentration in white clover herbage and dry matter yield per clover plant were reduced, for the most part, when a competing grass was present. The amount of nitrogen fixed per plant of white clover decreased markedly with temperature. Low temperature consequently accentuated competition for nitrate. The capacity of white clover to compete successfully was limited by its slower growth and nitrogen accumulation.     

Uptake of organic matter by the roots of sweet potato: Analysis of the δ14C value of plants

Summary To determine whether sweet potato (Ipomoea batatas (L.) Poir.) takes up organic matter through the roots from the medium, the concentrations of natural¹⁴C (¹⁴C) in plant organic matter, atmospheric CO₂ and compost applied to media were examined under soil and sand culture conditions. In these experiments, three kinds of composts of different ¹⁴C were used. CO₂ derived from the mineralization of compost was continuously pumped out from the pots and its direct uptake by the leaves was prevented.¹⁴C of plant parts harvested after the 43 days experimental period were affected by the ¹⁴C of the compost in the treatments where the compost of rice straw was applied, and which suggested that a significant amount of plant carbon was derived from the compost.     

The uptake,distribution, and translocation of86Rb in alfalfa plants susceptible and resistant to the bacterial wilt and the effect ofCorynebacterium insidiosum upon these processes

Alfalfa (Medicago sativa; L.) plants susceptible (S) and resistant (R) to the bacterial wilt were fedvia roots with a nutrient solution labelled with⁸⁶Rb⁺, at different times after inoculating them withCorynebacterium insidiosum (McCull.) H. L. Jens. The infection did not influence⁸⁶Rb⁺ uptake per plant in the course of a 14-day-period following inoculation, however it did affect its distribution differentially in the S- and the R-plants.⁸⁶Rb⁺ uptake was significantly decreased due to the infection in the S-plants on the day 49 after the inoculation (a 4-h-exposure to⁸⁶Rb⁺), with the iona also being more slowly translocated to the shoots in diseased S-plants than in diseased R-plants. Likely factors causing these effects and their relationship to alfalfa resistance to the bacterial wilt are discussed.     

Factors which affect the amount of inorganic phosphate, phosphorylcholine, and phosphorylethanolamine in xylem exudate of tomato plants

Phosphate in the xylem exudate of tomato (Lycopersicon esculentum) plants was 70 to 98% inorganic phosphate (Pi), 2 to 30% P-choline, and less than 1% P-ethanolamine. Upon adding ³²Pi to the nutrient, Pi in xylem exudate had the same specific activity within 4 hours. P-choline and P-ethanolamine reached the same specific activity only after 96 hours. The amount of Pi in xylem exudate was dependent on Pi concentration in the nutrient and decreased from 1700 to 170 micromolar when Pi in the nutrient decreased from 50 to 2 micromolar. The flux of 0.4 nmoles organic phosphate per minute per gram fresh weight root into the xylem exudate was not affected by the Pi concentration in the nutrient solution unless it was below 1 micromolar. During 7 days of Pi starvation, Pi in the xylem exudate decreased from 1400 to 130 micromolar while concentrations of the two phosphate esters remained unchanged.

The concentration of phosphate esters in the xylem exudate was increased by addition of choline or ethanolamine to the nutrient solution, but Pi remained unchanged. Upon adding [¹⁴C]choline to the nutrient, 10 times more [¹⁴C]P-choline than [¹⁴C]choline was in the xylem exudate and 85 to 90% of the ester phosphate was P-choline. When [¹⁴C]ethanolamine was added, [¹⁴C]P-ethanolamine and [¹⁴C]ethanolamine in the xylem sap were equal in amount. P-choline and P-ethanolamine accumulated in leaves of whole plants at the same time and the same proportion as observed for their flux into the xylem exudate. No relationship between the transport of P-choline and Pi in the xylem was established. Rather, the amount of choline in xylem exudate and its incorporation into phosphatidylcholine in the leaf suggest that the root is a site of synthesis of P-choline and P-ethanolamine for phospholipid synthesis in tomato leaves.

     

Respiration from C3 plant green manure added to a C4 plant carbon dominated soil

Application of tree leaves (C₃ plants) on maize (Zea mays L.) (C₄ plant) fields is an agroforestry management technology to restore or maintain soil fertility. The rate at which the tree leaves decompose is crucial for the nutrient supply to the crop. We studied the in situ decomposition of Sesbania sesban (L.) Merr. leaves or C₃ sugar for 4 – 8 days after application to a maize field in Kenya. By using the difference of around 10‰ in natural abundance of ¹³C between the endogenous soil C (mainly C₄) and the applied C (C₃), we could calculate the contributions of the two C sources to soil respiration. The δ¹³C value of the basal respiration was from –15.9 to –16.7‰. The microbial response to the additions of leaves and sugar to this tropical soil was immediate. Application of sesbania leaves gave an initial peak in respiration rates that lasted from one to less than 6 days, after which it levelled off and remained about 2 – 3 times higher (230–270 mg C m^-2 h^-1) than the control respiration rates throughout the rest of the experiment (5 – 8 days). In the sugar treatment, there was no initial peak in respiration rate. The respiration rate was 170 mg C m^-2 h^-1 after 4 days. At the end of the experiments, after 4–8 days, as much as 14–17% of the added C had been respired and about 60% of the total respiration was from the added sesbania leaves or C₃ sugar. This non-destructive method allows repeated measurements of the actual rate of C mineralisation and facilitates decomposition studies with high temporal resolution in the field. This revised version was published online in August 2006 with corrections to the Cover Date.     

Allocation of carbon to shoots,roots, soil and rhizosphere respiration by barrel medic (Medicago truncatula) before and after defoliation

The allocation of carbon to shoots, roots, soil and rhizosphere respiration in barrel medic (Medicago truncatulaGaertn.) before and after defoliation was determined by growing plants in pots in a labelled atmosphere in a growth cabinet. Plants were grown in a ¹⁴CO₂-labelled atmosphere for 30 days, defoliated and then grown in a ¹³CO₂-labelled atmosphere for 19 days. Allocation of ¹⁴C-labelled C to shoots, roots, soil and rhizosphere respiration was determined before defoliation and the allocation of ¹⁴C and ¹³C was determined for the period after defoliation. Before defoliation, 38.4% of assimilated C was allocated below ground, whereas after defoliation it was 19.9%. Over the entire length of the experiment, the proportion of net assimilated carbon allocated below ground was 30.3%. Of this, 46% was found in the roots, 22% in the soil and 32% was recovered as rhizosphere respiration. There was no net translocation of assimilate from roots to new shoot tissue after defoliation, indicating that all new shoot growth arose from above-ground stores and newly assimilated carbon. The rate of rhizosphere respiration decreased immediately after defoliation, but after 8 days, was at comparable levels to those before defoliation. It was not until 14 days after defoliation that the amount of respiration from newly assimilated C (¹³C) exceeded that of C assimilated before defoliation (¹⁴C). This revised version was published online in June 2006 with corrections to the Cover Date.     

Uptake of 3HHO and 32P by roots of wheat and rape

Summary Direct measurements were made of ³HHO and ³²P taken up from labelled soil by roots of wheat (Triticum aestivum L.) and rape (Brassica campestris L.). Single roots were encased in labelled soil for 3 days, and the amount of ³HHO and ³²P retained in the shoots was determined. Plants were grown to five stages of maturity in growth boxes under controlled conditions. Roots were labelled at up to four depths (to 90 cm) depending on the rooting depth at each stage of maturity. Uptake of ³HHO per unit length of root increased as the plant age increased, while uptake of ³²P decreased to below detection levels by 45 days after germination. Larger amounts of both nutrients were translocated to and retained in the shoots from surface roots than from roots located deeper in the soil although the soil was uniform in temperature, bulk density, and composition throughout the growth boxes. Wheat roots were more efficient than rape roots in absorbing ³HHO; however, rape roots took up larger amounts of ³²P per unit length of root. Neither native nor added P located more than 30 cm deep is of much importance to these annual crops, since uptake is minimal and the main demand for this nutrient occurs at early growth stages when the root system is restricted to the surface layers. re]19750812     

Effect of nitrate infusion into the shoot apoplast on photosynthesis and assimilate transport in symplastic and apoplastic plants

The shoots of fireweed (Chamerion angustifolium (L.) Holub) and common flax (Linum usitatissimum L.) were infused with 50 mM KNO₃ solution to compare the influence of nitrate on photosynthesis and assimilate export from leaves in plants with the symplastic and apoplastic phloem loading, respectively. The infusion of nitrate in the shoots of both plant species lowered ¹⁴CO₂ fixation and enhanced the assimilate transport in the upward direction. Irrespective of the phloem loading type, the incorporation of ¹⁴C into sucrose decreased in nitrate-treated seedlings exposed to assimilation for short (3 min) periods. However, when shoots were sampled 3 h after ¹⁴CO₂ fixation, the content of ¹⁴C-labeled sucrose was higher in treated plants than in control seedlings infused with water. In fireweed, in contrast to flax, a similar temporal pattern was also characteristic for ¹⁴C incorporation into oligosaccharides. Within 3 h after nitrate infusion into the fireweed apoplast, the mitochondria and the cell vacuolar system underwent ultrastructural changes indicative of the increase in cytosolic osmotic pressure. At the same time, we observed accumulation of fibrillar inclusions in cell vacuoles of vascular bundles. It is concluded that the mechanisms of nitrate influence on photosynthesis and sugar export in leaves of symplastic and apoplastic plants are similar to a certain extent and involve the blocking of pores in phloem tubes, initiated by the NO-signaling system.     

Fixation and distribution of 14C in Populus deltoides during dormancy induction

Photosynthetically fixed ¹⁴C was analyzed in various chemical fractions from leaves and stems of cottonwood (Populus deltoides Bartr. ex. Marsh.) during dormancy induction. Dormancy was induced by 8-h photoperiods and 20/14°C temperature regimes. Within 4 weeks under short days, terminal buds were set and leaf expansion and stem elongation had stopped. ¹⁴C₂ was fed to a leaf at Leaf Plastochron Index 7 for 30 min. Either after this 30 min feeding period or after a 48-h translocation period the plants were sampled, freeze-dried, extracted and analyzed for¹⁴C. ¹⁴C-fixation decreased during dormancy induction from 60% to 17% of the 3.7 MBq ¹⁴C applied at 0 week and 8 weeks, respectively. Percentage distribution of ¹⁴C in chemical fractions of source leaves reflected leaf age and translocation inhibition. In rapidly growing plants, considerable ¹⁴C was incorporated into leaf protein while most of the soluble¹⁴C-sugars were either metabolized or translocated out of the leaf. After terminal bud set, the percentage of ¹⁴C in the protein and residue fractions decreased rapidly and that in the sugar fraction increased. Percent distribution in stems closely reflected changing metabolic pathways of carbon flow as influenced by dormancy induction. For example, the ¹⁴C in structural carbohydrates decreased in 5 weeks under short days from 65 to less than 10% of the ¹⁴C recovered in the chemical fractions, thus indicating cambium inhibition. At the same time the percentage of ¹⁴C in starch and sugar increased indicating storage. Short term (after 30 min) incorporation of ¹⁴C into the protein and starch fractions of leaves changed relatively little throughout the 8-week induction period. In contrast the turnover rates of these fractions (¹⁴C present after 48 h) increased considerably after active growth of the whole plant stopped.     

Distribution of assimilated carbon in plants and rhizosphere soil of basket willow (Salix viminalis L.)

Willow is often used in bio-energy plantations for its potential to function as a renewable energy source, but knowledge about its effect on soil carbon dynamics is limited. Therefore, we investigated the temporal variation in carbon dynamics in willow, focusing on below-ground allocation and sequestration to soil carbon pools. Basket willow plants (Salix viminalis L.) in their second year of growth were grown in pots in a greenhouse. At five times during the plants growth, namely 0, 1, 2, 3 and 4 months after breaking winter dormancy, a subset of the plants were continuously labelled with ¹⁴CO₂ in an ESPAS growth chamber for 28 days. After the labelling, the plants were harvested and separated into leaves, first and second year stems and roots. The soil was analysed for total C and ¹⁴C content as well as soil microbial biomass. Immediately after breaking dormancy, carbon stored in the first year stems was relocated to developing roots and leaves. Almost half the newly assimilated C was used for leaf development the first month of growth, dropping to below 15% in the older plants. Within the second month of growth, secondary growth of the stem became the largest carbon sink in the system, and remained so for the older age classes. Between 31 and 41% of the recovered ¹⁴C was allocated to below-ground pools. While the fraction of assimilated ¹⁴C in roots and root+soil respiration did not vary with plant age, the amount allocated to soil and soil microbial biomass increased in the older plants, indicating an increasing rhizodeposition. The total amount of soil microbial biomass was 30% larger in the oldest age class than in an unplanted control soil. The results demonstrate a close linkage between photosynthesis and below-ground carbon dynamics. Up to 13% of the microbial biomass consisted of carbon assimilated by the willows within the past 4 weeks, up to 11% of the recovered ¹⁴C was found as soil organic matter.     

Routes of Ethephon Uptake in Pineapple (Ananas comosus) and Reasons for Failure of Flower Induction

Ethylene-releasing agents such as ethephon (2-chloroethylphosphonic acid) are used widely to induce flowering in pineapples (Ananas comosus (L.) Merrill). However, ethephon treatment is less reliable in summer, particularly if plants are treated on abnormally hot days. [¹⁴C]ethephon was used to follow uptake and translocation in leaf tissues. Up to 30% of the ethephon entered the leaf within 4 h, and up to 60% by 24 h. Uptake was dramatically modified by temperature, relative humidity, solution pH, and the surface on which solution droplets were placed. Entry occurred across the leaf cuticle and probably also by way of stomatal pores, and label was recovered at all depths within the leaf. ¹⁴C label entered more rapidly through the abaxial epidermis than through the adaxial epidermis. Low-volume spray applications to whole plants resulted in rapidly drying droplets mainly on the adaxial, distal epidermis and were rather ineffective at inducing flowering, possibly because little ethephon or ethylene reaches the shoot apex. High-volume sprays may facilitate ethephon entry because solution accumulates in leaf axils and hence remains in prolonged contact with abaxial epidermis of leaf bases close to the shoot apex. When poured into the center of the plant, 20% of a normal commercial ethephon dose induced full flowering even under adverse temperatures. It is suggested that high-volume evening spraying and avoidance of hot days may reduce the incidence of flowering failure. Received March 20, 1998; accepted September 6, 1999     

Differential Absorption, Translocation and Metabolism of Metribuzin [4-amino-6-tert-butyl-3-(methylthio)-as-triazine-5(4H)one] by Soybean Cultivars

Soybean (Glycine max (L.) Merr.) cultivars have been reported to range in tolerance to injury by 4-amino-6-tert-butyl-3-(methylthio)-as-triazine-5(4H)one (metribuzin), from tolerant (e.g.‘Bragg’) to susceptible (e.g.‘Coker 102’ and ‘Semmes’). ‘Bragg,’‘Coker 102’, and ‘Semmes’ soybeans were grown in sand subirrigated with nutrient solution containing labelled (¹⁴C-carbonyl metribuzin) and nonlabelled metribuzin to determine cultivar variability in absorption, translocation, and metabolism of metribuzin. Plants were periodically harvested, autoradiographed, and radioactivity in tissue extracts quantified. Data indicated that all 3 cultivars readily absorbed and translocated metribuzin. However, ‘Bragg’ tissues accumulated greater quantities of metribuzin metabolites than the other two cultivars. The major ¹⁴C-containing metabolite in ‘Semmes’ and ‘Coker’ roots and stems was 6-tert-butyl-as-triazine-3-5-(2H,4H)-dione, whereas the major ¹⁴C-metabolite isolated from‘Bragg’ roots and stems was a glucose conjugate. Results indicated that differential-intraspecific responses to metribuzin may result from differential capacities for herbicide detoxification by conjugation.     

Specificity of 1-triacontanol as a plant growth stimulator and inhibition of its effect by other long-chain compounds

The effect of several analogs of 1-triacontanol (TRIA), differing in C-chain length (16–32), the position of the hydroxyl group and the terminal functional group, were tested alone and in combination with TRIA on the growth of rice (Oryza sativa L.), maize (Zea mays L.) and tomato (Lycopersicon esculentum Mill.) seedlings. Applied alone, none of the compounds caused an increase in growth; thus, chain length (30 C) and presence and position (terminal) of the hydroxyl group appear to be specific for the growth-promoting activity of TRIA. When applied simultaneously with TRIA, all analogs inhibited the response to the latter in all three test plants, whether applied in the nutrient solution, as foliar spray or by seed soaking. 1-Octacosanol inhibited the response of rice seedlings to 2.3 x 10^-8 M TRIA at concentrations as low as 2.4 x 10^-12 M. Thus preparations of TRIA and application equipment must be free from trace amounts of other long-chain compounds if they are to be used to increase plant growth.Abbreviation TRIA 1-triacontanol     

Comparative Effects and Concentration of Picloram, 2,4,5-T and Dicamba in Tissue Culture

In nutrient agar comparative concentrations (10^?3 to 10^?5M) of (2,4,5-trichlorophenoxy)acetic acid (2,4,5-T) were generally more inhibitory to the growth of tissue cultures of soybean (Glycine max (L.) Merrill cv. Acme) and cottonwood (Populus deltoides Marsh.) than were either 4-amino-3,5,6-trichloropicolinic acid (picloram) or 3,6-dichloro-o-anisic acid (dicamba). Compared to untreated tissue dicamba or picloram at 10^?6M in the nutrient agar resulted in a 200 % increase in the growth of soybean tissue. At 10^?5 and 10^?6M dicamba also produced an increase in the growth of cottonwood tissue. Greatest absorption of picloram and dicamba by tissue cultures from agar occurred during the first 24 h after treatment. However, absorption remained nearly static thereafter for 14 days. More dicamba was absorbed by soybean and cottonwood tissue cultures than either picloram or 2,4,5-T.     

Factors Affecting Dalapon Absorption and Translocation in Johnsongrass

The factors affecting the absorption and translocation of ¹⁴C-dalapon (2.2-dichloropropionic acid) in johnsongrass were studied. Johnsongrass [Sorghum halepense (L.) Pers.] was first pot-grown in a greenhouse and then treated and placed in controlled-environment chambers. Absorption of ¹⁴C-dalapon into johnsongrass leaves and subsequent translocation occurred continuously within the plant during a 48-h period after treatment. Gas chromatographic analysis of johnsongrass extracts showed that the dalapon molecule was translocated intact. Absorption and translocation of ¹⁴C-dalapon increased as the droplet volume of the diluent was increased from 0.2 to 5.0 μl per treated spot. At 21 and 32°C, translocation of ¹⁴C-dalapon from a 2-cm treated leaf section into the plant was greater at 100% than at 35% relative humidity. At 38°C, translocation was greater at 35% than at 100% relative humidity. The addition of 0.5% surfactant to the dalapon solution increased translocation under all environmental conditions studied. The addition of 0.1 M KH₂PO₄ to dalapon-surfactant solutions increased ⁴-dalapon translocation under high temperature (38°C), especially at 35% relative humidity.