How Much AMS Do I Need to Combat Hard Water Antagonism of Postemergence Herbicides?

We have received a few questions this winter and spring about ammonium sulfate (AMS) rates to use with postemergence herbicides and how much is needed to overcome hard water issues.  Because of lower commodity prices and grower interest in keeping input expenses as low as possible, I thought it would be a good time to review this topic and the AMS equation to help applicators and farmers plan for spring and summer herbicide applications.

First, we would like to review the reasons for using ammonium sulfate with postemergence herbicide treatments.  It is fairly well-known that the weed control efficacy of many weak acid herbicides like glyphosate, 2,4-D, clethodim (Select and others), glufosinate (Liberty and others) can be reduced when water sources contain hard water cations like calcium (Ca+2), iron (Fe+3), magnesium (Mg+2), and sodium (Na+).  The hard water cations, which have a positive charge, will bind to the negatively charged herbicide molecule and reduce the herbicide’s ability to be absorbed into the plant.  Sometimes we call this process chelating and it is well known that glyphosate can chelate Ca2+ ions, and that calcium can tie up multiple glyphosate molecules (Figure 1).  To correct this problem, when you add AMS (NH4)2SO4 to the tank, the ammonium (NH4+) disassociates from the sulfate (SO4-2) and the sulfate preferentially binds to the positively charged hard water cations.  The sulfate essentially sequesters the hard water cations and prevents them from binding to the herbicide (Figures 2 and 3).  Additionally, after antagonistic minerals are neutralized by the sulfate, the ammonium can bind with the herbicide to form the ammonium herbicide salt, which can more effectively pass through the plant cuticle resulting in greater herbicide absorption, in some cases increased herbicide translocation, and overall greater herbicide efficacy.  This ‘physiological’ effect of AMS enhancing foliar herbicide activity even in the absence of hard water is important to keep in mind when considering adjuvant products that contain less ammonium, yet claim to be a replacement for AMS.

A simple formula was developed by weed scientists at North Dakota State University to show the minimum amount of AMS needed to overcome hard water antagonism.  Since we know which hard water cations are most problematic (K, Na, Ca, Mg, Fe), it is fairly easy to calculate the amount of ammonium sulfate needed to condition the water to reduce the negative implications of hard water antagonism.

The minimum amount of AMS needed to tie up hard water cations is calculated with this formula:

lbs AMS/100 gal =  (0.002 X ppm K)
+ (0.005 X ppm Na)
+ (0.009 X ppm Ca)
+ (0.014 X ppm Mg)
+ (0.042 X ppm Fe)

While this formula can be used to overcome the hard water cations in the spray solution (spray tank), the formula does not take into account hard water cations on plant leaf surfaces, which are fairly prevalent.  Many plants, such as velvetleaf (Figures 4 and 5), contain Ca on the leaf surface, and additional sulfate is needed to overcome the antagonism which can occur after the spray solution leaves the nozzle.  It is difficult to calculate the amount of ammonium sulfate needed to overcome Ca on the leaf surface.  This is the reason why herbicide labels typically contain statements that indicate that rates of AMS, 8 ½ to 17 pounds of AMS per hundred gallons of water, are recommended on many glyphosate labels.  Since AMS has typically been a low cost spray water conditioner, the additional amount added to a spray tank has not been viewed as a major expense.  However, in this era of low commodity prices and pressure on farmers to reduce input expenses, there may be an opportunity to reduce the amount of AMS applied and not compromise herbicide activity.  It is highly likely that AMS rates can be reduced to the lower end of the recommended rate and herbicide activity will not be compromised.  However, we would advise that it will be important to understand your water hardness test levels before severely reducing AMS rates.

Please keep in mind that the benefit of AMS goes beyond conditioning hard water since improved weed control with herbicides and AMS can even be observed when using de-ionized (distilled) water.  Thus, a good rule of thumb would be to add more AMS to your spray solution than what is specifically calculated above for your hard water to account for this ‘physiological’ benefit and fall within the herbicide label requirements for AMS.

 Figure 1. Glyphosate molecules in hard water.


Figure 1. Glyphosate molecules in hard water.

 

Figure 2. Glyphosate molecules in hard water plus Ammonium Sulfate (AMS).

Figure 2. Glyphosate molecules in hard water plus Ammonium Sulfate (AMS).

 

Figure 3. Effect of hard water cations on herbicide efficacy of weak acid herbicides.

Figure 3. Effect of hard water cations on herbicide efficacy of weak acid herbicides.

 

Figure 4. Effect of Ammonium Sulfate (AMS) on velvetleaf control with glyphosate in the greenhouse.

Figure 4. Effect of Ammonium Sulfate (AMS) on velvetleaf control with glyphosate in the greenhouse.

Figure 5. Effect of Ammonium Sulfate (AMS) on velvetleaf control with glyphosate in the field.

Figure 5. Effect of Ammonium Sulfate (AMS) on velvetleaf control with glyphosate in the field.

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