The economic effect of applying phosphorus at planting of durum wheat is directly correlated to the phosphorus that is available to the plants from the soil. In 1998 a study was done on a field with a bicarbonate soluble phosphorus level of 4.8 ppm, an a sizeable return on the phosphorous fertilizer investment was seen. In 1999 the test field had a phosphorous level of 13.0 ppm and as the University guidelines indicated, returns on phosphoroud expenditures were small. Negative returns were seen with barley and an increase of $61/ac was seen with 400 pounds of 16-20-0 on wheat.

Proper nutrient management is necessary for successful production of durum wheat in the desert. If grain protein content is less than 13 %, significant economic losses to growers can result. Late season nitrogen (N) fertilization can resolve this problem, but tissue test guidelines have not yet been established. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N, (ii) determine the minimum NO₃-N concentration in lower stem tissue at heading associated with the critical grain protein content, and (iii) determine whether flag leaf head, or whole plant total N at heading can be used as indicators of N status. In November 1998 three varieties of durum wheat, Mohawk, Kronos, and Westbred 881, were planted at the Maricopa Agricultural Center. Five N rates (0, 100, 200, 300, and 400 lbs/A) were applied in four split applications. Each treatment was replicated three times in a randomized complete block design. Samples were collected from the lower stem, flag leaf head, and whole plant from each plot at heading and analyzed for total N. Grain yields ranged from 1937 to 6174 lbs /A for Mohawk, 1706 to 6161 lbs/A for Kronos, and 864 to 5162 lbs/A for Westbred 881. Grain protein content averaged 5.7% to 14.0% for Mohawk, 7.3% to 13.7% for Kronos, and 7.9% to 14.5% for Westbred 881. Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.88 for Mohawk, 0.94 for Kronos, and 0.98 for Westbred 881. The critical NO₃-N concentration in the sap associated with >13% grain protein was 550 -770 ppm at heading for three varieties. Lower dried stem tissue critical NO₃-N concentration for Kronos was 4500 ppm NO₃-N, 4700 ppm NO₃-N for Mohawk, and 3600 ppm NO₃-N for Westbred 881 for a grain protein content of 13 %. Nitrogen concentration in flag leaves, heads, and whole plants were highly correlated with N rate. Therefore, N concentration in these tissues could potentially be used as indicators of late-season N status.

Malting barley is not a widely planted crop in the Southwest, due to grain protein contents that can sometimes exceed the industry standard of 11.4 %. To achieve < 11.4% grain protein, careful nitrogen (N) management is needed. Tissue testing guidelines for N management for reduced grain protein and acceptable yields have not yet been determined for malting barley in the Southwest. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N, and (ii) develop stem NO₃-N guidelines for N management in malting barley. In November 1998 two varieties of malting barley, Morex and Crystal, were planted at the Maricopa Agricultural Center. Five N rates (0, 60, 120, 180, and 240 lbs/acre) were applied in four split applications. Each treatment was replicated three times in a randomized complete block design. Samples were collected from lower stems at the 3-4 leaf 2 node, and flag leaf visible growth stages. Grain yields ranged from 1011 lbs/A to 2677 lbs/A for Morex and 827 lbs/A to 2641 lbs/A for Crystal. Grain protein ranged from 6.94 -11.5% (Morex) and 8.48-13.0% (Crystal). Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.83 for Morex and 0.85 for Crystal. For Morex and Crystal, grain protein was within the malting industry grain protein range of 10.5-11.4% and yield was optimized at 180 lbs N/A. Sap NO₃ analysis can be a useful tool for determining N status of malting barley.

Ironite and phosphorus were applied to plots seeded to hard red wheat and barley to find their effect on crop yield and nutrient uptake at various stages of crop development. Phosphorous caused significant increases in yield in both wheat and barley, where Ironite caused few changes in yield. Ironite caused significant increases in percent of nutrients stored in barley grain, but generally had little effect on nutrient uptake by plants at boot or milk stage. Phosphorous tended to decrease the percent nutrient uptake by plants.

The standard procedure for determining nitrogen (N) status in small grains is to sample lower stem tissue for nitrate (NO₃) analysis. The tissues are then submitted to a laboratory for analysis. Sap nitrate (NO₃) can be analyzed in the field, immediately after collecting the sample, using a Cardy meter. Guidelines for sap analysis have not yet been determined. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N , and (ii) develop sap NO₃ test guidelines for N management in durum and feed barley. In November 1998 one variety of durum (Kronos) and one variety of feed barley (Gustoe) were planted at the Maricopa Agricultural Center. Three N rates (80, 200, and 400 lbs N/acre) were applied in four split applications. Each treatment was replicated five times in a randomized complete block design. Samples were collected from lower stems at the 3-4 leaf 2 node, flag leaf visible, and heading growth stages. Grain yields ranged from 4330 lbs/A to 6794 lbs/A for Kronos and 3220 lbs/A to 4533 lbs/A for Gustoe. Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.76 for Kronos and 0.60 for Gustoe. Sap NO₃-N analysis can be used to determine N status during the season for Kronos. Results for the barley suggest at low concentrations of NO₃ in the lower stem, the Cardy meter may underestimate NO₃ concentrations. This may be due to changes in moisture content in the stem as the season progresses.

Proper nutrient management is necessary for successful production of durum wheat in the desert. If grain protein content is less than 13 %, significant economic losses to growers can result. Late season nitrogen (N) fertilization can resolve this problem, but tissue test guidelines have not yet been established. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N, (ii) determine the minimum NO₃-N concentration in lower stem tissue at heading associated with the critical grain protein content, and (iii) determine whether flag leaf head, or whole plant total N at heading can be used as indicators of N status. In November 1997 two varieties of durum wheat, Mohawk and Kronos, were planted at the Maricopa Agricultural Center. Five N rates (0, 100, 200, 300, and 400 lbs/A) were applied in four split applications. Each treatment was replicated three times in a randomized complete block design. Samples were collected from the lower stem, flag leaf head, and whole plant from each plot at heading and analyzed for total N. Grain yields ranged from 1663 to 6916 lbs/A for Mohawk and 1529 to 7060 lbs/A for Kronos. Maximum yields were achieved at 200 lbs N/A for both varieties. Grain protein content averaged 8.6% to 13.4% (Mohawk) and 9.1% to 13.8% (Kronos). Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.96 for Mohawk and 0.97 for Kronos. Lower stem sap critical NO₃-N concentration in Kronos is 1100 ppm NO3 N and 1700 ppm NO₃-N for Mohawk at heading for a grain protein content of 13 %. Lower dried stem tissue critical NO₃-N concentration in Kronos is 5500 ppm NO₃-N and 7500 ppm NO₃-N for Mohawk for a grain protein content of 13 %. Nitrogen concentration in flag leaves, heads, and whole plants were highly correlated with N rate. Therefore, N concentration in these tissues could potentially be used as indicators of late-season N status.

The standard procedure for determining nitrogen (N) status in small grains is to sample lower stem tissue for nitrate (NO₃) analysis. The tissues are then submitted to a laboratory for analysis. Sap nitrate (NO₃) can be analyzed in the field, immediately after collecting the sample, using a Cardy meter. Guidelines for sap analysis have not yet been determined. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N, and (ii) develop sap NO₃ test guidelines for N management in durum and feed barley. In November 1997 one variety of durum (Kronos) and one variety of feed barley (Gustoe) were planted at the Maricopa Agricultural Center. Three N rates (80, 200, and 400 lbs N/acre) were applied in four split applications. Each treatment was replicated five times in a randomized complete block design. Samples were collected from lower stems at the 3-4 leaf 2 node, flag leaf visible, and heading growth stages. Grain yields ranged from 5185 lbs/A to 7156 lbs/A for Kronos and 6314 lbs/A to 7517 lbs/A for Gustoe. Maximum yields were achieved at 200 lbs N/A for both varieties. Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.79 for Kronos and 0.84 for Gustoe. Sap NO₃-N analysis can be used to determine N status during the season for both Kronos and Gustoe.

The economic effect of applying phosphorus at planting of durum wheat is directly correlated to the phosphorus that is available to the plants from the soil. For bicarbonate soluble phosphorus levels less than 6 ppm, there will likely be a positive economic effect from applying some phosphorus. At this site the soil phosphorus level was 4.8 ppm and the application of 200 pounds of 16-20-0 caused an increase in yield of 2101 pounds per acre. A cost of $23 per acre with a return of $168 per acre.

Grain quality is important to growers and buyers of durum. Growers are usually docked if their HVAC drops below 90% or their grain protein is below 13 %. The purpose of this study was to demonstrate the ability of nitrogen fertilizer application near flowering to increase HVAC and grain protein. Six commercial sites were chosen for this study and Kronos was the variety. The application of about 50 pounds of nitrogen per acre increased HVAC by from 81 to 93% and increased grain protein from 11.2 to 12.3% on average, similar to results obtained in the past.

Malting barley is not a widely planted crop in the Southwest, due to grain protein contents that can sometimes exceed the industry standard of 11.4 %. To achieve < 11.4% grain protein, careful nitrogen (N) management is needed. Tissue testing guidelines for N management for reduced grain protein and acceptable yields have not yet been determined for malting barley in the Southwest. The objectives of this study were to: (i) correlate NO₃-N in dried stem tissue with sap NO₃-N, and (ii) develop stem NO₃-N guidelines for N management in malting barley. In November 1997 two varieties of malting barley, Morex and Crystal, were planted at the Maricopa Agricultural Center. Five N rates (0, 60, 120, 180, and 240 lbs/acre) were applied in four split applications. Each treatment was replicated three times in a randomized complete block design. Samples were collected from lower stems at the 3-4 leaf 2 node, and flag leaf visible growth stages. Grain yields ranged from 1765 lbs/A to 3439 lbs/A for Morex and 2104 lbs/A to 4274 lbs/A for Crystal. Grain protein ranged from 7.6- 10.5% (Morex) and 7.0- 10.7% (Crystal). Correlation coefficients between stem NO₃-N and sap NO₃-N were 0.80 for Morex and 0.84 for Crystal. For Morex and Crystal, grain protein was within the malting industry grain protein range of 10.5- 11.4% at 240 lbs N/A, and yield was optimized at 180 lbs N/A. Sap NO₃ analysis can be a useful tool for determining N status of malting barley. Stem NO₃-N concentrations at 180 lbs N/A were generally within the optimum range for NO₃-N in small grains.