2006 Annual Report

Agronomy Section

Dickinson Research Extension Center
1089 State Avenue
Dickinson, ND 58601

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Spring Wheat Seed Treatment Demonstration-Dunn and Stark Counties, North Dakota

R.O. Ashley, D. Barondeau, and G. Martin

Summary

Three experimental products at three different rates and two registered products at labeled rates were evaluated at two southwest North Dakota locations for the control of fungal root and crown diseases on hard red spring wheat (Triticum aestivum L. c.v. Parshall) by comparing disease, growth, and yield parameters of treated plots to an untreated check plot at two southwest North Dakota locations.

Introduction

Seeds may be treated with fungicides for various reasons. These reasons include: 1) prevention of disease development because of seed-borne infection by pathogenic microorganisms; 2) protecting seeds and seedlings from invasion by soil-borne seedling invaders; and 3) protecting the plant from specific soil-borne pathogens that cause root and crown rots. A number of protectant or systemic seed treatments are registered for wheat seed treatment. Some are specific for certain seed or soil-borne fungi; others are wider spectrum. Often several products are used in combination or are formulated to provide control of a wider spectrum of diseases.

Soil-borne fungi and seed treatments are affected by individual or local soil environments so field demonstrations under local conditions are prudent. The purpose of this study was to demonstrate the ability of fungicide seed treatments to control root and crown pathogens in a continuous wheat rotations.

Methods

The demonstrations were conducted on the Jay Elkin Farm near Taylor, ND, (Stark County) at a site that had been in continuous wheat for the previous five years and on the Larry Pavlicek Farm near Dickinson, ND (Dunn County) at a site that had been in wheat the previous year. At the Stark County site winter wheat was seeded in the fall of 2003 and eliminated from the plot area on 9 Apr with an application of Roundup Ultra Max at the rate of 20 fl oz/acre + 40 fl oz/acre Actamater (ammonium sulfate) spray adjuvant. The soil is a Morton silty clay loam. The soil was sampled on 2 Apr 2004 and analyzed at the NDSU Soil Testing Laboratory. The soil analysis indicated the soil contained 15 lbs/acre NO3-N, 7 ppm P, 380 ppm K, 48 lbs/acre SO4-S and 139 lbs/acre Cl. Organic mater content at the site was 3.9% and pH was 6.0. Urea at the rate of 220 pounds per acre was broadcast applied on 16 Apr 2004. Significant rainfall occurred the following day.

The Dunn County site was seeded on a Regent silty clay loam. The soil was sampled on The soil was sampled on 7 Apr 2004 and analyzed at the NDSU Soil Testing Laboratory. The soil analysis indicated the soil contained 63 lbs/acre NO3-N, 16 ppm P, 290 ppm K, 24 lbs/acre SO4-S and 75 lbs/acre CL. Ammonium sulfate at the rate of 150 pounds per acre was broadcast when the crop was at the three-leaf stage on 2 Jun.

A randomized complete block design with four replications was used at each location. Plots were 10 feet wide by 45 feet long with a four-foot buffer of winter wheat seeded between each plot.

Parshall hard red spring wheat was treated with one of three experimental seed treatment fungicides at three different rates prior to planting (Table 1) or one of two registered products at the labeled rate. Seed planted in the check (CHECK) plot was untreated. No-till production practices were used at each location. Seed was planted with a Cross-Slot no-till drill on 27 Apr at the Stark County site and on 29 Apr at the Dunn County site at the rate of 1.5 million seed per acre.

One post-emergent herbicide application was used to control weeds in the crop. This application was made on 8 Jun 2004 with a tank mix of 0.5 oz/acre of Harmony GT XP + 0.66 pt/acre of Puma. In addition to the herbicides 2 fl oz/acre of Tilt was applied at the same time for foliar disease control.

Emergence evaluations were conducted when approximately 50% of the plants had emerged in the untreated plot on 19 May 2004 and the emergence completed count was may on 26 May 2004. Plant counts in three 4.9 m sections of row were collected and plants per square meter were calculated.

Root and crown samples from four plots per treatment were evaluated twice during the growing season. The first evaluation occurred between Zadoks 24 and 28 (tillering) and the second evaluation occurred at Zadoks 85 (soft dough). For the first evaluation, 15 plants were carefully dug from each plot and excess soil gently shaken from the roots. Samples were stored with the soil still on the roots in plastic bags and refrigerated until washed and analyzed. Plants selected for the first evaluation were evaluated for stage of development; length of the plant measured from the crown to the tip of the last fully extended leaf, extent of lesions on the subcrown internode, and counts of both seminal and crown roots. Twenty-five plants for the second evaluation were carefully dug and excess soil gently shaken from the roots. The samples were stored with the soil still on the roots and refrigerated until the roots were washed and evaluated. For the second evaluation, subcrown internode, root color, and root mass were examined.

During Zadoks 85 (soft dough), soil from each of the untreated CHECK plots was sampled by discarding the first 5 cm of soil from the surface and retaining the next 5 cm of soil for the sample. These samples were then combined, mixed and a subsample placed in a plastic bag and submitted to Ribeiro Plant Lab, Inc., Bainbridge Island, WA for analysis of Pythium, Fusarium, and Rhizoctonia propagules. Pythium presence and levels were determined using a modification of the PARPH medium published by Jeffers and Martin (1986); Fusarium presence and levels were determined using Komada’s medium (Komada, 1975); and Rhizoctonia presence and levels were determined using MKH at 1:1000 dilution (Sneth, 1991). Propagule counts for Bipolaris sorokiniana, the cause of common root rot, were not done.

Prior to harvest, mature plant height and head densities were determined. The Taylor plots were harvested on 24 Aug and the Dickinson Plots were harvested on 30 Aug with a Massy Ferguson 8XP combine, which measured grain weight harvested, percent moisture of harvested grain, and grain test weight. Harvested area was measured and yields were calculated. Protein was determined at Southwest Grain Inc., Dickinson, ND. Grain yield, test weight, and protein were adjusted to 12% moisture basis (Hellevang, 1986).

All data were statistically analyzed using SAS Statistical software version 8.2.

Results and Discussion

Emergence

No significant differences in emergence were detected at either location (Table 2). As the application rate for KNF 2829 increased, stand counts tended to decrease.

Grain Yield, Test Weight, Protein and Head Density

KNF 2826 at 400 ml/100 Kg of seed produced the highest grain yield of any seed treatment in this trial and was significantly higher than the untreated CHECK (Table 3). All grain test weights were considered low and no significant differences in protein were detected. Rainfall was 43% of normal for the entire growing season. June was the second driest ever recorded in the 108 year history of the Dickinson weather station with only 12% of normal or 0.46 inches of rainfall measured for that month. August precipitation was 36% of normal and was probably not sufficient to produce normal test weight grain. Head densities for KNF 2826 significantly decreased as application rates increased for this product. The other experimental products did not exhibit a change in head density as application rates changed.

Root Evaluations

During the initial root evaluation, plant length and crop development stage tended to decrease as application rates of KNF 2826 and KNF 2827 increased, although not significantly (Table 4). Seminal root counts decreased as application rates increased for KNF 2827.

The subcrown internode ratings in the second evaluation were lower for all seed treatments, except KNF 2826 at the 300 ml/Kg rate (Table 5). Root mass tended to be larger but not significantly larger than the check for all seed treatments except Dividend XL, which was lower than the CHECK.

Propagule counts (Ribeiro 2004) were noted at medium levels for Pythium spp (250 ppg), Fusarium spp (520 ppg) and Rhizoctonia spp (20 ppg) at the Taylor site. Propagule counts at the Dickinson site for Pythium spp. were high (490 ppg), Fusarium spp. were medium (600 ppg) and no Rhizoctonia spp. were detected. This may explain some of the treatment by location and location interactions found in this trial.

Implications of Demonstration

KNF 2826 applied at the rate of 400 ml/100 Kg had a significantly better subcrown internode rating at the soft dough stage and higher yield than the CHECK. In addition to these ratings, KNF 2826 tended to produce higher test weight grain, improved tiller counts, subcrown internode ratings, seminal root counts and crown root counts at the Zadoks 24, and improved root color and root mass at Zadoks 85 when compared to the CHECK. However, this product decreased the number of heads produced per unit area as application rates increase.

The KNF 2826 fungicide seed treatment appears to provide some protection from Pythium spp. and Biolaris sorokiniana and provides better protection from soil-borne pathogens than the currently registered products used in this demonstration.

Cooperating Producer and Financial Support

The authors wish to thank Jay Elkin for providing the use of his land to this trial. In addition, the authors wish to extend a thank you to Crompton Uniroyal Chemical Company for their financial support of this trial.

The following individuals assisted with collecting the data: Heidi Schmierer, Samatha Roth, Tina Partin, Joshua Seekins, Jean Pippert Dustin Roberts, Tina Hirsch and David Ell.

Literature Cited

Helevang, K.J. 1986. Grain moisture content effects and management. AE-905. Cooperative Extension service, North Dakota State University, Fargo, ND.

Jeffers, S.N., and S.B. Martin. 1986. Comparison of two media selective for Pytophthora and Pythium species. Plant Disease. 70:1038-1043.

Komada, H. 1975. Development of selective media for quantitative isolation of Fusarium oxysporum for natural soil. Rev. Plant Port. Res. 8:114-125.

Ribeiro, O.K. 2004. Personal communication 11 Nov 2004.

SAS Institute 2001. Release 8.2 ed SAS Institute, Inc., Cray, NC.

Sneh B., L. Burpee, and A. Ogoshi. 1991. Identification of Rhizoctonia species. APS Press, St. Paul, MN. 133p.

 

 

 

 

 

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