Heterodera glycines Ichinohe is a serious pest of soybean [Glycine max (L.) Merr.] in the USA. Several Races of H. glycines occur in the soybean growing areas. Soybean accessions with resistance to Races 3, 5, and 14 have been identified. Data on reaction of these accessions for Races 1 and 2 are not available. Our objective was to bioassay these accessions for resistance to H. glycines Races 1 and 2. Eighty‐six accessions, host differentials, and susceptible control were bioassayed during 1995 to 1996 for each of the two Races in thermoregulated water baths in the greenhouse. The results indicated that 52 accessions had resistance to H. glycines Race 1, and 24 accessions had resistance to Race 2, respectively. Soybean PIs 89772, 90763, 404166, 404198A, 437654, 437690, 438489B, 567491A, and 567516C were either resistant or moderately resistant to both Races. These are potential resistance sources to H. glycines Races 1, and 2 for developing resistant soybean cultivars. These PI lines are being fingerprinted by means of molecular markers to identify the unique lines to allow broadening the diversity of resistance gene utilization.
Field experiments were conducted at locations in northern and southern Illinois, central Iowa, and central Missouri from 1997 to 1999 to investigate the effects of Heterodera glycines on soybean growth, development, and yield. A wide range of infestation levels was present at all locations. Two locally adapted cultivars, one resistant to H. glycines, were grown at each location. Cultivars were planted in alternating four-row strips with 76 cm between rows. For each cultivar, 20 1-m-long single-row plots were sampled every 2 weeks starting 4 weeks after planting. Infection by H. glycines reduced plant height and leaf and stem weight on the resistant cultivars in the first 12 weeks after planting, and delayed pod and seed development 12 to 14 weeks after planting. Biomass accumulation was not reduced on the susceptible cultivars until 10 weeks after planting; reduction in pod and seed development occurred throughout the reproductive stages. Susceptible cultivars produced significantly lower yields than resistant cultivars, but the yield reductions were not accompanied by visually detectable symptoms.
Crop growth models are tools with valuable uses in research synthesis and crop management. This paper discusses genetic coefficients in the CROPGRO–Soybean model in terms of definitions, implications for genetic improvement, relationships to field performance, and linkage to genomics. As used in crop models, genetic coefficients are mathematical constructs designed to mimic the phenotypic phenotypic outcome of genes under different environments to influence: (i) life cycle including fractional allocation to different phases, (ii) photosynthetic, (iii) vegetative, (iv) rooting, and (v) reproductive processes. Model sensitivity analyses was used to hypothesize genetic coefficients of soybean [Glycine max (L.) Merr.] and impact on field performance. Yield improvement from increased leaf photosynthesis was shown to be small if coupled to specific leaf weight. Yield improvement with longer seed filling duration was enhanced by traits such as slower N mobilization to sustain leaf photosynthesis or by genetic traits and management factors allowing adequate leaf area index before seed fill. Yield improvement under water‐deficit appeared feasible from rate of root‐depth increase, shift in root profile, and a slow senesce trait. Modeled genetic coefficients showed mostly additive effects on yield when evaluated in combinations; and combinations of minor changes gave yield increases of 13 to 17%, comparable to recent genetic improvement. More than additive effects occurred under good crop management or under projected rise in global CO2. Information from genomics, physiology, and yield performance trials can be used to derive genetic coefficients for crop models. Interaction of molecular geneticists, physiologists, and crop modelers is needed to facilitate the translation of genetic knowledge to modes of action, and finally to integrated field performance under multiple stress environments.
During 1997, the first year of widespread use of glyphosate (N‐[phosphonomethyl]glycine) on Roundup Ready (RR) soybean [Glycine max (L.) Merr.] a severe sudden death syndrome (SDS) epidemic occurred and several RR cultivars were affected. Effects of glyphosate on colonization of soybean root by Fusarium solani (Mart.) Sacc f. sp. glycines (Fsg) and SDS were evaluated. Five RR cultivar pairs that contrasted for SDS resistance from maturity groups (MG) II to VI were evaluated with and without glyphosate application. The MG II and III cultivars were evaluated near Bloomington, Pontiac, and Mahomet in central Illinois and the MG IV, V, and VI cultivars were evaluated near Harrisburg, Ullin, and Valmeyer in southern Illinois. The Fsg root infection severity (IS), colony forming units per gram of root (CFU), SDS leaf scorch disease index (DX), and grain yield were determined. Across environments within each MG, there were no significant effects of glyphosate on IS, CFU, and DX. Significant differences were expected between cultivars but only observed in some MG. There was no significant effect of glyphosate on yield. Significant Glyphosate × Cultivar interactions occurred for yield in MG VI, in favor of the glyphosate sprayed subplots. In this study root colonization by Fsg and SDS leaf symptoms did not significantly increase following the application of glyphosate. Data from this study indicate that the development of SDS on RR soybean is influenced by genotype. Farmers planting RR soybean in Fsg infested fields are encouraged to select cultivars with resistance to SDS.
Soybean sudden death syndrome (SDS), caused by Fusarium solani f. sp. glycines, is a problem in some soybean-growing areas in the United States. Resistance is an important control strategy. In this study, root colonization of six soybean cultivars by F. solani f. sp. glycines was determined. Cultivars included susceptible P3981, CM497, and Spencer and field resistant LS90-1920, Pharaoh, and Ripley. All cultivars were tested in field experiments at different locations in southern Illinois in 1997 and 1998. Roots were collected at six sampling times and were dried and ground to isolate and enumerate the pathogen on a selective medium. SDS foliar disease index (FDX), the area under the F. solani f. sp. glycines population curve (AUPC), the incidence of colonized roots at 45 days after planting (RCI45), and the root colonization rate (RCR) were used to compare cultivars. FDX on the three resistant cultivars was significantly lower than on the three susceptible cultivars. Means of AUPC on the three resistant cultivars were significantly lower than those on the susceptible CM497 and P3981. RCI45 of Pharaoh was significantly lower than those of P3981 and Spencer. RCRs of all three resistant cultivars were significantly lower than that of P3981, and RCR of Ripley was also significantly lower than that of CM497. Based on combination of all cultivars, AUPC was significantly correlated with RCI45 and RCR.
Field studies were conducted to determine the relationships between soybean yield and foliar disease index (FDX) of sudden death syndrome (SDS) as well as root colonization by Fusarium solani f. sp. glycines, the causal agent. Single-row plots in a soybean field with relatively uniform SDS incidence and severity were identified at growth stage R6 on cultivar Pioneer 9492 in DeSoto, IL, in 1997 and 1998. For each plot, foliar disease index (FDX), yield, and yield components were determined. In 1997, linear relationships between yield (Y, grams per meter of row) and FDX were obtained from the wide-row (Y = 207.84 - 1.09 FDX) and narrow-row (Y = 126.66 - 0.745 FDX) plots, respectively. A linear relationship (Y = 124.23 - 1.11 FDX) also was observed in 1998. Increase in each FDX unit caused yield loss from 18 to 29 kg/ha (0.7 – 1.1 g/m of row). FDX was negatively correlated with seed weight (grams per plant) in both years and with seed size (grams per 100 seeds) in 1997. A no-tilled field at Southern Illinois University planted to soybean cultivar Asgrow 5403 was divided into 25 plots in 1997 and 40 plots in 1998. Root samples were taken from each plot at five or six sampling times during the seasons. Roots were used to isolate and enumerate F. solani f. sp. glycines on a selective medium to obtain the CFU. FDX was assessed and soybean yield was obtained from each plot. Soybean yield correlated negatively with FDX in both years. Both yield and FDX correlated significantly with CFU from slightly before growth stage R1 to R2 in both years, and with area under the pathogen population curve (AUPC) in 1997. An increase in one unit of AUPC or CFU per gram of root at R6 was associated with yield loss of 0.19 or 0.014%, respectively.
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