scholarly journals Spray mixture pH as affected by dicamba, glyphosate, and spray additives

2019 ◽  
Vol 33 (4) ◽  
pp. 547-554 ◽  
Author(s):  
Thomas C Mueller ◽  
Lawrence E Steckel
Keyword(s):  
Critical Value ◽  
Minor Effect ◽  
Solution Ph ◽  
Ph Change ◽  
Limited Effect ◽  
Mixed Response ◽  
Spray Solution ◽  
Initial Ph ◽  
Carrier Volume ◽  
A Minor

AbstractThe pH of spray mixtures is an important attribute that affects dicamba volatility under field conditions. This report examined the effect of different components added to water sources that ranged in initial pH from 4.6 to 8.4. Commercial products were used, which include formulations of dicamba, glyphosate, the drift retardant Intact, ammonium sulfate (AMS), and several pH modifiers. Adding BAPMA salt of dicamba always increased the mixture pH, whereas diglycolamine + VaporGrip® (DGA+VG) had a mixed response. The addition of AMS decreased pH slightly (usually <0.5 pH unit), whereas the addition of potassium salt of glyphosate (GLY-K) always decreased the measured pH (from 1.0 to 2.1 pH units). A substantial pH change could have profound effects on dicamba volatility. Moreover, the 1.0 to 2.1 pH units would not be consistent with the registrant’s report stating that GLY-K decreased mixtures with DGA+VG pH by only 0.2 to 0.3 units. The drift retardant Intact had no effect on pH. There was no difference in resultant pH when comparing K salt and isopropylamine (IPA) salts of glyphosate. Spray carrier volume, ranging from 94 to 187 L ha–1, had only a minor effect on measured pH after the addition of various spray components. The addition of selected pH modifiers raised the pH above 5.0, which is a critical value according to the latest dicamba application labels. The order of mixing of various pH modifiers, including AMS, had only limited effect on measured spray solution pH.

scholarly journals A Theoretical and Experimental Study of Electrochemical pH Control at Gold Interdigitated Microband Arrays

2021 ◽  
Author(s):  
Bernardo Patella ◽  
Robert Daly ◽  
Ian Seymour ◽  
Pierre Lovera ◽  
James Rohan ◽  
...  
Keyword(s):  
Electrode Array ◽  
Ph Control ◽  
Reduction Peak ◽  
Solution Ph ◽  
Ph Indicator ◽  
Ph Change ◽  
Initial Ph ◽  
The Impact ◽  
Strong Acids

In electroanalysis, solution pH is a critical parameter that often needs to be adjusted and controlled for the detection of particular analytes. This is most commonly performed by the addition of chemicals, such as strong acids or bases. Electrochemical in-situ pH control offers the possibility for the local adjustment of pH at the point of detection, without additional reagents. FEA simulations have been performed to guide experimental design for both electroanalysis and in-situ control of solution pH. No previous model exists that describes the generation of protons at an interdigitated electrode array in buffered solution with one comb acting as a protonator, and the other as the sensor. In this work, FEA models are developed to provide insight into the optimum conditions necessary for electrochemical pH control. The magnitude of applied galvanostatic current has a direct relation to the flux of protons generated and subsequent change in pH. Increasing the separation between the electrodes increases the time taken for protons to diffuse across the gap. The final pH achieved at both, protonators and sensor electrodes, after 1 second, was shown to be largely uninfluenced by the initial pH of the solution. The impact of buffer concentration was modelled and investigated. In practice, the pH at the electrode surface was probed by means of cyclic voltammetry, i.e., by cycling a gold electrode in solution and identifying the potential of the gold oxide reduction peak. A pH indicator, methyl red, was used to visualise the solution pH change at the electrodes, comparing well with the model’s prediction

The Influence of Adjusting Spray Solution pH on the Efficacy of Saflufenacil

2013 ◽  
Vol 27 (3) ◽  
pp. 445-447 ◽  
Author(s):  
Jared M. Roskamp ◽  
William G. Johnson
Keyword(s):  
Ammonium Sulfate ◽  
Weight Reduction ◽  
Seed Oil ◽  
Dry Weight ◽  
Final Solution ◽  
Solution Ph ◽  
Field Corn ◽  
Spray Solution ◽  
Initial Ph ◽  
Water Ph

Saflufenacil solubility and efficacy has been shown to be influenced by carrier water pH. This research was conducted to determine if altering the pH of a solution already containing saflufenacil would influence the efficacy of the herbicide. Saflufenacil at 25 g ai ha−1was applied to field corn in carrier water with one of five initial pH levels (4.0, 5.2, 6.5, 7.7, or 9.0) and then buffered to one of four final solution pH levels (4.0, 6.5, 9.0, or none) for a total of twenty treatments. All treatments included ammonium sulfate at 20.37 g L−1and methylated seed oil at 1% v/v. Generally, saflufenacil with a final solution pH of 6.5 or higher provided more dry weight reduction of corn than saflufenacil applied in a final pH of 5.2 or lower. When applying saflufenacil in water with an initial pH of 4.0 or 5.2, efficacy was increased by raising the final solution pH to either 6.5 or 9.0. Conversely, reduction in corn dry weight was less when solution pH of saflufenacil mixed in carrier water with an initial pH of 6.5 or 7.7 was lowered to a final pH of 4.0. When co-applying saflufenacil with herbicides that are very acidic, such as glyphosate, efficacy of saflufenacil may be reduced if solution pH is 5.2 or lower.

Mechanisms of aluminum tolerance in Triticum aestivum (wheat). IV. The role of ammonium and nitrate nutrition

1985 ◽  
Vol 63 (12) ◽  
pp. 2181-2186 ◽  
Author(s):  
Gregory J. Taylor ◽  
Charles D. Foy
Keyword(s):  
Triticum Aestivum ◽  
Phase Ii ◽  
Aluminum Tolerance ◽  
Triticum Aestivum L ◽  
Al Tolerance ◽  
Solution Ph ◽  
Ph Change ◽  
Initial Ph ◽  
Nutrient Solutions

Five cultivars of Triticum aestivum L. (wheat) were grown for 21 days in solution cultures with aluminum (+Al) (74 μM) and without Al (−Al) at an initial pH of 4.5. Patterns of nitrogen depletion and pH change were biphasic. Ammonium [Formula: see text] was rapidly depleted and solution pH declined during phase I. Depletion of nitrate [Formula: see text] was most rapid and solution pH increased after [Formula: see text] was exhausted from solutions (phase II). Cultivar tolerance to Al was negatively correlated with the rate of pH decline induced by cultivars, and the rate of pH decline was positively correlated with the rate at which cultivars depleted [Formula: see text] from +Al and −Al nutrient solutions. Cultivar tolerance to Al was also negatively correlated with the rate of [Formula: see text] depletion from +Al and −Al solutions. Cultivar tolerance to Al was positively correlated with the rate of [Formula: see text] depletion during phase II but only when plants were grown with Al. These results support the hypothesis that differential Al tolerance among cultivars of T. aestivum is caused by differences in the rate of [Formula: see text], and possibly [Formula: see text], uptake. Such diffferences in N preference may have caused differences in pH and Al solubility in the nutrient solutions.

scholarly journals An Inquiry into the Phenomenon of Enhanced Transport of Pesticides Caused by Effluents

1995 ◽  
Author(s):  
Ellen R. Graber ◽  
Linda S. Lee ◽  
M. Borisover
Keyword(s):  
Soil Solution ◽  
Dissociation Constants ◽  
Acid Dissociation ◽  
Minor Effect ◽  
Column Studies ◽  
Solution Ph ◽  
Flow Paths ◽  
Water Flow Velocity ◽  
Pesticide Transport ◽  
A Minor

The objective of this collaborative research project was to determine the factors that may cause enhanced pesticide transport under effluent irrigation. For s-triazines, the potential for enhanced transport through association with effluent dissolved organic matter (OM) was shown to be small in batch and column studies and in numerical simulations. High alkalinity and pH of treated effluents increased soil-solution pH for selected soil-effluent combinations, promoting the dissolution of soil OM and mobilizing otherwise OM-retained pesticides. Evapotranspiration in column studies resulted in increased pore-water concentrations of dissolved OM and some pesticide transport enhancement with the greatest effect observed with OM-poor soils. For ionogenic pesticides, effluent-induced increases in soil-solution pH increased the mobility of pesticides with acid dissociation constants within 2 pH units of the initial soil-solution pH. Effluents high in suspended solids and/or monovalent cations resulted in blockage of soil pores reducing water-flow velocity and/or changing flow paths. Reduced flow resulted in an increase in desorption time of soil sorbed pesticides, increasing the amount available for further transport with the net effect being soil texture dependent. In terms of pesticide degradation in soils, effluents appeared to have only a minor effect for the few pesticides investigated.

scholarly journals A Theoretical and Experimental Study of Electrochemical pH Control at Gold Interdigitated Microband Arrays

2021 ◽  
Author(s):  
Bernardo Patella ◽  
Robert Daly ◽  
Ian Seymour ◽  
Pierre Lovera ◽  
James Rohan ◽  
...  
Keyword(s):  
Electrode Array ◽  
Ph Control ◽  
Reduction Peak ◽  
Solution Ph ◽  
Ph Indicator ◽  
Ph Change ◽  
Initial Ph ◽  
The Impact ◽  
Strong Acids

In electroanalysis, solution pH is a critical parameter that often needs to be adjusted and controlled for the detection of particular analytes. This is most commonly performed by the addition of chemicals, such as strong acids or bases. Electrochemical in-situ pH control offers the possibility for the local adjustment of pH at the point of detection, without additional reagents. FEA simulations have been performed to guide experimental design for both electroanalysis and in-situ control of solution pH. No previous model exists that describes the generation of protons at an interdigitated electrode array in buffered solution with one comb acting as a protonator, and the other as the sensor. In this work, FEA models are developed to provide insight into the optimum conditions necessary for electrochemical pH control. The magnitude of applied galvanostatic current has a direct relation to the flux of protons generated and subsequent change in pH. Increasing the separation between the electrodes increases the time taken for protons to diffuse across the gap. The final pH achieved at both, protonators and sensor electrodes, after 1 second, was shown to be largely uninfluenced by the initial pH of the solution. The impact of buffer concentration was modelled and investigated. In practice, the pH at the electrode surface was probed by means of cyclic voltammetry, i.e., by cycling a gold electrode in solution and identifying the potential of the gold oxide reduction peak. A pH indicator, methyl red, was used to visualise the solution pH change at the electrodes, comparing well with the model’s prediction

Effects of CO2on Spray Solution pH

1995 ◽  
Vol 9 (1) ◽  
pp. 23-28 ◽  
Author(s):  
Michael P. Braverman ◽  
James L. Griffin
Keyword(s):  
Deionized Water ◽  
Bicarbonate Concentration ◽  
Solution Ph ◽  
Spray System ◽  
Spray Solution ◽  
Initial Ph ◽  
Recovery From Acidification ◽  
Rate Of Recovery ◽  
Ph Decrease ◽  
Ph Range

The pH of deionized water, initially adjusted to a pH of 6 to 9, all decreased to near pH 5 upon pressurization with CO2in a backpack spray system. When deionized water contained bicarbonate (NaHCO3or KHCO3) at 0 to 800 mg/L to buffer against a pH decrease from CO2pressurization the return to their initial pH was more rapid than deionized water alone regardless of bicarbonate source. Acidification of spray solution following CO2pressurization of 138, 276, or 414 kPa was similar and bicarbonate had a greater effect than spray pressure. Addition of acidifying buffer and bicarbonate to the solution resulted in an initial and post-CO2pressurization pH range of less than one pH unit. All spray solution pH levels returned to near their initial pH following depressurization, indicating that the pH decrease was not permanent. Rate of recovery from acidification with CO2increased with initial pH and bicarbonate concentration.

Effect of pH and NH4NO3 as a Spray Additive on Penetration of NAA Through Isolated Tomato Fruit Cuticle

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 550a-550 ◽  
Author(s):  
Royal G. Fader ◽  
Martin J. Bukovac
Keyword(s):  
Direct Measurement ◽  
Sodium Citrate ◽  
Tomato Fruit ◽  
Initial Slope ◽  
Control Effect ◽  
Solution Ph ◽  
Ph Change ◽  
Effect Of Ph ◽  
Spray Droplets ◽  
Partition Behavior

We have reported that NH4NO3 (AN, 8 mM, pH 4.2), applied as simulated spray droplets, enhanced penetration of 14C-NAA through isolated leaf and fruit cuticles. One explanation for this response is that AN depresses NAA (pKa= 4.2) dissociation, increasing the nondissociated moiety, which penetrates more readily than the anion (NAA'). Direct measurement of AN (concn. 0-800 mM) effect on NAA (215 μM) dissociation as indexed by change in solution pH revealed no significant effect, with a pH change from 4.19 to 4.05. This change is not sufficient to account for the observed enhancement. When 14C-NAA, buffered (20 mM sodium citrate) at pH 3.2, 4.2, 5.2, 6.2, was partitioned against chloroform, there was a marked increase in NAA partitioning into chloroform as pH was decreased. AN (8 mM) did not alter this partition behavior, also indicating no effect on NAA dissociation. However, in cuticle penetration studies, using a finite dose system with 14C-NAA buffered at pH 3.2, 4.2, 5.2, 6.2, and in the presence and absence of 8 mM AN, there was no marked or consistent pH or AN (-70 to + 232 % of no AN control) effect on penetration as indexed by initial slope (4-12 h) or penetration after 120 h. The possible effects of AN and buffer on penetration of 14C-NAA from the droplet deposit will be discussed.

Improvement of monitoring of tertiary filtration with particle counting

2006 ◽  
Vol 6 (1) ◽  
pp. 1-9
Author(s):  
V. Miska ◽  
J.H.J.M. van der Graaf ◽  
J. de Koning
Keyword(s):  
Particle Surface ◽  
Minor Effect ◽  
Particle Size Distributions ◽  
Particle Volume ◽  
Mass Distributions ◽  
Particle Counting ◽  
Total Particle ◽  
Particle Counts ◽  
A Minor ◽  
Sample Dilution

Nowadays filtration processes are still monitored with conventional analyses like turbidity measurements and, in case of flocculation–filtration, with phosphorus analyses. Turbidity measurements have the disadvantage that breakthrough of small flocs cannot be displayed, because of the blindness regarding changes in the mass distributions. Additional particle volume distributions calculated from particle size distributions (PSDs) would provide a better assessment of filtration performance. Lab-scale experiments have been executed on a flocculation–filtration column fed with effluent from WWTP Beverwijk in The Netherlands. Besides particle counting at various sampling points, the effect of sample dilution on the accuracy of PSD measurements has been reflected. It was found that the dilution has a minor effect on PSD of low turbidity samples such as process filtrate. The correlation between total particle counts, total particle volume (TPV) and total particle surface is not high but is at least better for diluted measurements of particles in the range 2–10 μm. Furthermore, possible relations between floc-bound phosphorus and TPV removal had been investigated. A good correlation coefficient is found for TPV removal versus floc-bound phosphorus removal for the experiments with polyaluminiumchloride and the experiments with single denitrifying and blank filtration.

scholarly journals Linkage mapping identifies a non-synonymous mutation in FLOWERING LOCUS T (FT-B1) increasing spikelet number per spike

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jonathan Brassac ◽  
Quddoos H. Muqaddasi ◽  
Jörg Plieske ◽  
Martin W. Ganal ◽  
Marion S. Röder
Keyword(s):  
Flowering Time ◽  
Aspartic Acid ◽  
Synonymous Substitution ◽  
Minor Effect ◽  
Phenotypic Variance ◽  
Spikelet Number ◽  
Wheat Varieties ◽  
Trait Locus ◽  
A Minor ◽  
Spikelet Number Per Spike

AbstractTotal spikelet number per spike (TSN) is a major component of spike architecture in wheat (Triticumaestivum L.). A major and consistent quantitative trait locus (QTL) was discovered for TSN in a doubled haploid spring wheat population grown in the field over 4 years. The QTL on chromosome 7B explained up to 20.5% of phenotypic variance. In its physical interval (7B: 6.37–21.67 Mb), the gene FLOWERINGLOCUST (FT-B1) emerged as candidate for the observed effect. In one of the parental lines, FT-B1 carried a non-synonymous substitution on position 19 of the coding sequence. This mutation modifying an aspartic acid (D) into a histidine (H) occurred in a highly conserved position. The mutation was observed with a frequency of ca. 68% in a set of 135 hexaploid wheat varieties and landraces, while it was not found in other plant species. FT-B1 only showed a minor effect on heading and flowering time (FT) which were dominated by a major QTL on chromosome 5A caused by segregation of the vernalization gene VRN-A1. Individuals carrying the FT-B1 allele with amino acid histidine had, on average, a higher number of spikelets (15.1) than individuals with the aspartic acid allele (14.3) independent of their VRN-A1 allele. We show that the effect of TSN is not mainly related to flowering time; however, the duration of pre-anthesis phases may play a major role.

scholarly journals IL-6 Is Not Absolutely Essential for the Development of a TH17 Immune Response after an Aerosol Infection with Mycobacterium tuberculosis H37rv

Cells ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 9
Author(s):  
Kristina Ritter ◽  
Jan Christian Sodenkamp ◽  
Alexandra Hölscher ◽  
Jochen Behrends ◽  
Christoph Hölscher
Keyword(s):  
Immune Response ◽  
Inflammatory Diseases ◽  
Mycobacterial Infection ◽  
Minor Effect ◽  
Mycobacterium Tuberculosis H37rv ◽  
Th 17 ◽  
Anti Inflammatory ◽  
A Minor ◽  
Aerosol Infection ◽  
Deficient Mice

Anti-inflammatory treatment of chronic inflammatory diseases often increases susceptibility to infectious diseases such as tuberculosis (TB). Since numerous chronic inflammatory and autoimmune diseases are mediated by interleukin (IL)-6-induced T helper (TH) 17 cells, a TH17-directed anti-inflammatory therapy may be preferable to an IL-12-dependent TH1 inhibition in order to avoid reactivation of latent infections. To assess, however, the risk of inhibition of IL-6-dependent TH17-mediated inflammation, we examined the TH17 immune response and the course of experimental TB in IL-6- and T-cell-specific gp130-deficient mice. Our study revealed that the absence of IL-6 or gp130 on T cells has only a minor effect on the development of antigen-specific TH1 and TH17 cells. Importantly, these gene-deficient mice were as capable as wild type mice to control mycobacterial infection. Together, in contrast to its key function for TH17 development in other inflammatory diseases, IL-6 plays an inferior role for the generation of TH17 immune responses during experimental TB.

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