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Published in Crop Sci. 44:425-432 (2004).
© 2004 Crop Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA

CROP BREEDING, GENETICS & CYTOLOGY

Influence of Genotype, Environment, and Nitrogen Management on Spring Wheat Quality

E. J. Souzaa, J. M. Martin*,b, M. J. Guttieria, K. M. O'Briena, D. K. Habernichtb, S. P. Lanningb, R. McLeanc, G. R. Carlsond and L. E. Talbertb

a Univ. of Idaho Aberdeen Research and Extension Center, P.O. Box 870, Aberdeen, ID 83210
b Dep. of Plant Sci. and Plant Pathology, Montana State Univ., Bozeman, MT 59717-3140
c Pendleton Flour Mills, 463 W. Hwy 26, Blackfoot, ID 83221
d Northern Agric. Res. Center, Star Route No. 36, Box 43, Havre, MT 59501

* Corresponding author (jmmartin{at}montana.edu).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Bread baking is the primary end-use criterion used to select hard spring wheat (Triticum aestivum L.) genotypes for the northwestern USA, yet the use of hard wheats has expanded beyond traditional pan breads to include Asian noodles. We assessed the relative influence of genotype, N management, and location on quality characteristics of a set of spring wheat cultivars that provided a range in gluten strength and acceptability for bread and Asian noodle quality, and determined whether grain characteristics could predict bread and/or noodle market suitability. Seven spring cultivars were grown at four locations across 3 yr with two levels of N fertilizer in irrigated and moisture-limited conditions. Bread quality, alkaline noodle color, and Chinese noodle color and texture were assessed on grain samples. Cultivar was the most important determinant of bread and noodle quality traits in both the irrigated and moisture-limited environments. Nitrogen level influenced only Chinese noodle color in irrigated environments, but impacted test weight, flour ash, loaf volume, and bake absorption in moisture-limited environments. Responses to N management and location were usually not cultivar specific, as interactions were not important relative to main effects of cultivar and location. Grain protein had more value than test weight or grain hardness in predicting bread and noodle quality, and was most useful in predicting loaf volume and Chinese noodle color characteristics. Cultivar selection is critical for achieving a desired end use, with location effects being of secondary importance. Nitrogen management for a particular end use will be difficult, with N level being much less important than cultivar selection and location. Grain protein may be the best predictor of the suitability of a particular cultivar produced in a specific year for alternative end-use possibilities, with high-protein grain most suitable for bread production and low-protein, high-quality grain more suitable for noodle production.


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
A LIMITED NUMBER of crops are grown in the semiarid regions of the Pacific Northwest, with wheat being most widely grown because of adaptation and availability of reliable markets. Given the reliance on wheat production in the region, breeding efforts aimed at market diversification have developed wheat cultivars with diverse end-use properties, and thus distinct market channels. Hard red spring wheat is a predominant crop in much of this region where rainfall is limited, and is used primarily for domestic and international markets in bread manufacture. Desirable characteristics for hard red spring wheat include high protein and strong gluten (Souza et al., 2002). Soft white wheat is grown in regions with higher rainfall expectations or in arid areas with supplemental irrigation. Cookies and cakes are the target end-use products for most of the soft white crop. Desirable characteristics for this wheat class include low protein and limited damage to starch granules during milling that results in low-water-absorption flours (Guttieri et al., 2001a).

Recent cropping diversification has prompted development and deployment of hard white spring wheat in the Pacific Northwest of the USA. Asian customers desire hard white wheat for manufacturing noodles largely because of its brighter flour and product color (Hatcher and Kruger, 1993). Asian consumers use 30 to 45% of their wheat in noodles (Miskelly, 1996). Additionally, domestic bread bakers use hard white spring as an alternative to hard red spring. Advantages to hard white spring wheat derive from the absence of red seed coat pigments that are found in hard red spring wheat. Red pigmentation discolors flour at high extraction levels and subsequently taints noodle color. Additionally, the lack of the red pigment results in lighter-colored whole wheat bread products. The USA does not currently produce hard white spring wheat in quantities sufficient for the export market, and produces limited quantities for the domestic bread market.

The utility of hard white spring wheat in two markets (bread and noodles) provides marketing advantages and unique challenges. In particular, lower protein wheat is needed for noodle manufacture than is typically desired for making bread. Protein levels in wheat are influenced by cultivar (genotype), N management, and by environmental conditions. Growers may manipulate the first two factors through cultivar selection and N application. However, environmental conditions may work either in support or opposition to cultivar selection and management. For instance, despite N management for high yield and low protein, a low-rainfall season will tend to produce a crop with low yield and high protein.

The lack of environmental predictability, and to a certain extent market conditions, has made the idea of dual-purpose hard wheat attractive. That is, if the grain does not meet quality specifications for one use, there is potential for placement of the grain in the alternative market. Grain protein concentration is heavily influenced by genotype. Yet, a range in grain protein concentration may be obtained when the same cultivar is grown across a range of environments, thus producing grain with variable end-use qualities. A challenge is that genetic factors for noodle vs. bread quality may work in opposition. For instance, Lang et al. (1998) found that superior noodle color characteristics were negatively correlated with bread loaf volume in a set of hard white spring wheat genotypes tested across three environments. However, much of this negative relationship could be attributed to grain protein, in that high protein was associated with high loaf volume and poor noodle color (Lang et al., 1998). Similar results were found by Habernicht et al. (2002), with a set of hard winter wheat genotypes grown in several dryland environments.

For this report, we assessed the relative influence of genotype, N management, and location on quality characteristics of a set of spring wheat cultivars that provided a range in gluten strength and acceptability for bread and Asian noodle quality. Additionally, given the possibility of grain entering market channels for either bread or noodle production, we were interested to identify grain characteristics that may provide direction to growers and buyers as to market suitability.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Field Experiment
Seven spring wheat genotypes were selected for analysis across a range of environments. Genotypes included ‘Hi-Line’ (PI 549275) hard red (Lanning et al., 1992), ‘Idaho 377s’ (PI 591045) hard white (Souza et al., 1997), ‘Klasic’ hard white (PI 486139), MTHW9603 hard white, ‘Centennial’ (PI 537303) soft white (Souza et al., 1991), ‘Lolo’ (PI 614840) hard white (Souza et al., 2003), and ‘Pomerelle’ (PI 592983) soft white (Souza et al., 1997). Centennial, Idaho 377s, Klasic, and Lolo carry the null allele at the wx-b1 locus, which reduces the proportion of amylose compared with wild-type wheat starch. The seven genotypes represent a range in gluten strength. Hi-Line has strong gluten with good bread-baking qualities. Klasic, Idaho 377s, Lolo, and MTHW9603 were considered dual-purpose wheats with moderate gluten strength. The two soft wheats represent the low end of the spectrum for gluten strength. Genotypes were grown under irrigation at Aberdeen, ID, Bozeman, MT, and Tetonia, ID, in each of 3 yr (1998, 1999, and 2000), and under moisture-limited conditions at Aberdeen, Bozeman, Tetonia, and Havre, MT, in each of the same 3 yr. In each trial, three replications were grown in a split-plot arrangement, with cultivar being the main plot and fertility the subplot treatments. The fertility treatment involved N fertilization to optimal predicted yield potential, and fertilizing with 85% of the N needed to reach optimal predicted yield potential. An exception was that for Bozeman 1998, fertility was the main-plot treatment and cultivars were subplots. Therefore, the Bozeman 1998 data were not included in the analysis of variance, but were used in subsequent correlation analyses. Plots consisted of four 3-m rows at Bozeman, three 5-m rows at Havre, and seven 3-m rows at Aberdeen and Tetonia. Between-row spacing matched local commercial grain plantings, with Bozeman and Havre plots 30 cm and Aberdeen and Tetonia 17 cm between rows. Grain from each plot was harvested for quality analysis. A subsample of grain was used to determine test weight with a Seedburo (Chicago, IL) test weight scale. Kernel weight and grain hardness were determined with the Single Kernel Characterization System 4100 (SKCS) (Perten Instruments North America, Inc., Springfield, IL) with a sample of 300 kernels from each plot.

Milling and Baking Analysis
Total grain protein of samples was determined with a near-infrared analyzer (AACC Method 39-10A), calibrated by automated combustion analysis of total N content (Model NFP-428, LECO Corp., St. Joseph, MO), and corrected to 12% moisture. Samples were tempered (AACC Method 26-10) and milled with a Brabender Quadramat Senior Mill (AACC Method 26-21A). Flour protein concentration was determined by the same protocol as whole grain protein. With the Minolta CR-310 Chroma Meter (Ramsey, NJ), flour color was measured against the Commission Internationale de D'Elairage L*a*b* color scale. Brightness was measured by the L* axis, red-green colors by the a* axis, and yellow-blue colors by the b* axis.

Bread quality evaluations involved standard AACC mixograph and 100-g flour pup loaf tests (American Association of Cereal Chemists, 1995; Baley et al., 2001). Mixograph mixing time and absorption were scored for each sample. Tolerance to mixing was scored (1–8) by visual comparison of mixographs to standard mixograph reference charts, adjusted for protein content (Pomeranz, 1987). Dough was prepared for baking, noting water absorption and mixing time, by a protocol consistent with a 90-min, sugar-based fermented dough system. The bread formula contained 100 g flour, 6 g sugar, 3.5 g shortening, 1.8 g yeast, 1.5 g salt, 180 µg g–1 Doh-Tone (American Ingredients Co., Kansas City, MO), and 150 µg g–1 ascorbic acid oxidant. The finished loaves were analyzed for bake volume by measuring the displacement of canola seeds and crumb grain scored on a subjective 0 to 5 scale (5 = best).

Noodle Analysis
Chinese raw noodles were prepared by a method similar to Kruger et al. (1992) with the modifications described in Habernicht et al. (2002). Flour (100 g) was premixed at low speed on a National pup-loaf mixer for 1 min with 29.2 mL of a NaCl solution (4.29% w/v) during a 30-s time period. Mixing continued at medium speed for 5 min. Dough rested in a plastic bag for 30 min before sheeting with an Ohtake noodle machine (Ohtake Manufacturing Co., Ltd., Tokyo, Japan). Dough was folded and sheeted six times with a gap of 5 mm at 30°C. The dough rested 30 min before reduction sheeting, five reductions to a thickness of 1.2 mm. Dough sheets were stored in plastic bags at room temperature during evaluations. Noodle color was evaluated at 0 and 24 h after sheeting with the Minolta CR-310 Chroma Meter. The Chinese raw noodles were boiled and their texture profile after cooking evaluated as previously described (Lang et al. 1998, Habernicht et al. 2002). Texture characteristics (springiness, cohesiveness, adhesiveness, hardness, chewiness) were measured on five strands of rinsed noodles at 0 and 5 min after cooking with a TA-XT2 Texture Analyzer (Texture Technologies Corp., Scarsdale, NY) with a 6-mm flat Lexan probe.

Alkaline noodles were prepared as described in Guttieri et al. (2001b) by mixing 50 g flour to a crumbly consistency with 9 mL of alkaline salt solution (0.25% w/v Na2CO3, 1% NaCl) on a 35 g National pin mixer (National Manufacturing, Lincoln, NE) for 45 s. Dough was scraped down from the pins and bowl sides and mixed for another 45 s. Dough was collected and sheeted through an Atlas/Marcato (Wilton Industries, Woodridge, IL) hand-crank pasta maker at the zero (widest) setting for the first pass. The dough piece was folded twice and repeatedly passed through the sheeter until a sheet thickness of approximately 1.5 mm was achieved. The dough sheet was cut into three strips, stacked on a white tile, and measured for color at 0 and 24 h after sheeting as described for the Chinese raw noodles. Noodles were stored at room temperature in sealed plastic bags between color measurements.

Rapid Viscoanalysis of Flour Pasting
The flour pasting viscosity of each flour sample was determined with the Rapid Visco Analyser (Newport Scientific, Warriewood, NSW, Australia) to analyze 3 g of flour mixed with 25 mL of water. Pasting curves were determined with heating and mixing profiles from Guttieri et al. (2001a): flour suspension cycle of 10 s with a rotor speed of 960 rpm, followed by a 2-min pregelatinization step of 60°C at 160 rpm rotor speed (rotor speed held constant for all subsequent steps), a gelatinization step ramping the temperature to 93.5°C during a 6-min period, held at 93.5°C for a 4-min period, then cooled to 50°C for a 4-min period, and finally held at 50°C for 4 min. Peak flour pasting viscosity during the heating step was recorded in centipoise (cP = kg m2 s2), as were final viscosities during the 50°C holding cycle.

Statistical Analysis
The irrigated and rain-fed trials were analyzed independently by mixed effects analysis of variance with PROC MIXED in SAS (Littell et al., 1996). The analysis was combined across years, treating trial location, cultivar, and N as fixed effects and year, replication, and their interactions with location, cultivar, and N as random effects. Tests of significance of fixed effects were accomplished by combining the appropriate linear combination of mean squares using Satterthwaite's (Satterthwaite, 1946) approximation with the DDFM = SATTERTH option in PROC MIXED.

Relationships among grain traits with bread and noodle quality traits were computed with either grain protein, test weight, or grain hardness as independent variables and individual bread or noodle quality traits as dependent variables using the moisture regime x location x N combination means for each cultivar (n = 28). Heterogeneity of slope among cultivars was evaluated with regression analysis with PROC GLM in SAS (SAS Institute, 1988), by testing for the interaction of the class variable, cultivar, and the independent continuous variable. The relationships between grain traits and bread and noodle quality traits were presented as Pearson's linear correlation coefficients for ease of comparison across relationships, as tests of significance for linear regression coefficient and linear correlation are equivalent (Steel and Torrie, 1980).


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The 3 yr of research produced grain yield and grain protein concentration values that spanned the range normally found for spring wheat production within this region (Table 1). Average grain protein concentration ranged from 123 to 141 g kg–1 for the irrigated locations, and from 124 to 149 g kg–1 for the moisture-limited locations. The difference in grain protein concentration between high and low applied N was 8 and 5 g kg–1 for irrigated and moisture-limited locations, respectively. Among cultivars, hard red spring wheat Hi-Line had the highest average grain protein at 145 g kg–1, while soft white spring wheat genotypes Centennial and Pomerelle had the lowest average grain protein at 119 and 116 g kg–1, respectively. Grain yield showed similar variation, with irrigated locations varying between 4112 and 7070 kg ha–1, and moisture-limited locations varying between 2372 and 6984 kg ha–1. High vs. low applied N made little difference in final yield in the moisture-limited locations, and had a somewhat larger influence in the irrigated locations. Variation among genotypes for yield potential was more pronounced in irrigated than moisture-limited environments, with a range of >1500 kg ha–1 between the highest- (Pomerelle) and the lowest-yielding genotype (MTHW9603) in the irrigated environments and a range of approximately 550 kg ha–1 in the moisture-limited environments.


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Table 1. Spring wheat genotype, N level, and location means for selected traits in irrigated and moisture-limited environments averaged across 3 yr.

 
Loaf volume differences among environments, N levels, and genotypes tended to reflect grain protein differences with higher grain protein being associated with higher loaf volume in both the irrigated and moisture-limited environments (Table 1). The span within environments and between high and low N levels was less for moisture-limited than for irrigated environments for Chinese noodle hardness. Centennial, a soft white, and Hi-Line, a hard red, represented the low and high extremes for Chinese noodle hardness in both irrigated and moisture-limited environments. Mean Chinese noodle brightness (L*) at 24 h tended to be inversely related to grain protein mean values for locations and N level. Klasic and Pomerelle, both white wheats, represented darkest (lowest L*) and brightest (highest L*) Chinese noodles after 24 h in both types of environments.

Main Effects of Treatments
Genotype was consistently the most important determinate of quality traits in both the irrigated and moisture-limited environments (Tables 2 and 3). The exceptional traits were the initial brightness (L*) of alkaline noodles and flour yield in irrigated environments where differences among genotypes were nonsignificant. Locations within the irrigated trials affected protein concentration (grain and flour), bread crumb yellowness (b*), initial brightness of the alkaline noodles, and most of the characteristics of Chinese noodles (Table 2). In contrast, the moisture-limited sites produced significant location effects for protein concentration (grain and flour), flour yield, and bread crumb yellowness (b*), but none of the Chinese noodle characters. Loaf volume was also affected by location in the moisture-limited sites (Table 3).


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Table 2. Selected analysis of variance F values for irrigated trials showing sources of variation for selected quality traits for seven spring wheat genotypes, two N levels, and three locations for 3 yr.

 

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Table 3. Selected analysis of variance F values for moisture-limited trials showing sources of variation for key quality traits for seven spring wheat genotypes, two N levels, and three locations for 3 yr.

 
The level of N fertilization did not significantly affect grain yield in either irrigated or moisture-limited environments. In the high-N treatment, relative to the low-N treatment, flour protein concentration was increased by 7 g kg–1 in the irrigated environments (P < 0.05). No similar increase in grain or flour protein concentration was observed in the moisture-limited environments. However, test weight was reduced by the greater N fertility level (6 kg hL–1) in the moisture-limited trials (P < 0.01). Flour ash was not changed significantly in the irrigated trials, but increased 0.10 g kg–1 in the moisture-limited trials in the high-N treatment relative to the low-N treatment (P < 0.01). The limited response in protein concentration and the reduction in grain test weight in the moisture-limited environments suggest that the low-N treatments on average were adequate for the genotypes tested, and that higher levels of N in these trials did not have beneficial results. Although the N treatment did not significantly change the protein concentration in the moisture-limited trials, it did increase loaf volume by 30 mL and water absorption by 8 g kg–1 (P < 0.01) (Tables 1 and 3). No effect was observed on the loaf volume in the irrigated trials. In the irrigated trials, added N significantly altered Chinese noodle color by making them more dark at 0 and 24 h (L*) and more yellow (b*) (Table 2). No effect of N treatment on Chinese noodle color was observed in the moisture-limited trials (Table 3).

Interactions among Main Effects
Few of the quality or agronomic traits were influenced by interactions among the main effects of location, N, or genotype in either the irrigated or moisture-limited environments. Only grain protein concentration in the irrigated trials and noodle hardness in the moisture-limited trials had a significant three-way interaction among the main effects. When location interactions with genotype were observed, they were smaller than the effects of genotype. Graybosch et al. (1996) used the ratio of cultivar F values to interaction F values to assess the relative importance of genotype x environment interaction. Applying that analysis to this data set, the smallest ratio of genotype to genotype x location was found for initial brightness of alkaline noodles in irrigated environments. Genotypic effects were not significant for initial brightness, and the F value for genotypes was only 1.7 times the magnitude of the significant genotype x location interaction. Because of the interaction of genotype x environment, initial brightness of the alkaline noodles may be difficult to improve through selection in irrigated environments, and likely would be difficult to predict on the basis of knowledge of the mean performance of cultivars or the location. The next smallest ratio of F values was found for flour ash, where the F value for genotype was five and six times greater than the genotype x environment interaction in the irrigated and moisture-limited environments, respectively.

Prediction of End Use from Grain Characteristics
In this research, we wanted to improve the understanding of whole grain characteristics that may be predictive of bread and noodle quality, and to determine if those trait associations were similar across cultivars. Grain characteristics were predictive of several important bread-making traits within cultivars (Table 4). Grain protein was negatively associated with flour ash for all cultivars, but responses varied with cultivars where r values ranged from –0.22 for Centennial to –0.80 for Lolo (Table 4). Grain protein was highly predictive for loaf volume (mean r = 0.83) and water absorption (mean r = 0.59). Increased test weight was always associated with decreased mixograph tolerance, but response varied with cultivar, and r values ranged from –0.13 for Centennial to –0.72 for Lolo. Test weight showed predictive value for both water absorption (mean r = –0.34) and loaf volume (mean r = –0.46), where associations were always negative for all cultivars. On average, grain hardness was not a reliable predictor of mixograph tolerance, water absorption, or loaf volume. Cultivars differed in response for grain hardness with flour ash. Centennial and Pomerelle, both soft textured wheats, showed lower correlations than the hard wheats (Table 4).


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Table 4. Correlations of grain characteristics with important bread-making traits within seven spring wheat genotypes grown in 28 moisture regime x location x N level combinations.

 
Grain characteristics were correlated to noodle-making traits within cultivars (Table 5). Grain protein was most highly predictive of Chinese Noodle L* at 0 h (mean r = –0.79) and Chinese noodle L* change (0–24 h) (mean r = 0.81). Increasing grain protein was associated with decreasing L* at 0 h and with increasing change in L* between 0 and 24 h (less color stability). The grain protein–Chinese noodle L* change relation differed across cultivars where correlations ranged from 0.73 for Klasic to 0.91 for Pomerelle. Grain protein was also moderately predictive (mean r = 0.37) of Chinese noodle hardness, where cultivars differed in their responses with correlations ranging from –0.24 for Klasic to 0.69 for Pomerelle. Test weight was most highly predictive of Chinese noodle hardness (mean r = –0.46), with increased test weight being associated with decreased Chinese noodle hardness. The only instance where relationship between test weight and noodle traits was not similar across cultivars was for Chinese noodle L* at 0 h, where correlations ranged from –0.22 to 0.52. On average, grain hardness showed little promise in predicting alkaline noodle L* at 0 h, Chinese noodle springiness or Chinese noodle hardness with mean r < 0.13 in absolute value for each case. The predictive value of grain hardness varied among cultivars for Chinese noodle L* at 0 h and both alkaline and Chinese noodle L* change (0–24 h). Increasing grain hardness within cultivars was most often associated with increased Chinese noodle L* at 0 h, but decreased stability in L* (0–24 h) in both alkaline and Chinese noodles.


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Table 5. Correlations of grain characteristics with important Alkaline and Chinese raw noodle traits within seven spring wheat genotypes grown in 28 moisture regime x location x N level combinations.

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Wheat grown in the Pacific Northwest enters both domestic and international markets. Historically, hard wheat has been milled into white flour and used for baking bread. Although traditional pan bread is still a primary end use, there is increasing demand for hard wheat that is suitable for specialty bread products as well as for making Asian noodles (Miskelly, 1996). Soft white wheat is primarily grown in higher rainfall areas or under irrigation, and is used primarily for cookies and cakes in addition to Asian noodles. For these experiments, we wished to empirically determine the relative influence of location, N management, and genotype on the suitability of a diverse set of wheat genotypes for bread products and noodle production. In addition, our goal was to generate a range of values for bread and noodle traits for these selected genotypes that a wheat grower might expect to produce and market. The most striking observation concerning the effects of genotype and location is that genotype tended to be the predominant source of variation for most quality traits, illustrating the importance of cultivar selection in the management plan for growers. Additionally, this result points to the potential desirability of cultivar identification as a tool for grain buyers to select production lots for a specific end use. Location effects were significant for grain and flour protein in both irrigated and moisture-limited trials. In addition, locations influenced noodle brightness (L*) for the irrigated experiments. Previous analysis of soft wheat quality traits for Centennial and Pomerelle also concluded that genotype, followed by location, were the two most important factors determining pastry quality of the grain, while irrigation and fertility effects within an environment were significantly less important (Guttieri and Souza, 2003).

In contrast to most end-use quality traits, location differences overshadowed genotype differences for grain yield (Tables 1, 2, and 3). This implies that cultivar selection by growers may be more meaningful in terms of end-use quality than for grain yield. However, the current pricing system whereby farmers are not paid for end-use quality means that growers place greater emphasis on grain yield than end-use quality traits when selecting cultivars.

Level of applied N was rarely important for end-use quality traits (Tables 2 and 3). When N application was significant, such as for grain protein in irrigated trials, genotype and location still tended to be more important. The lack of predictable effect of applied N probably relates to the unpredictable nature of production. In our experiments, two levels of fertilization included recommended levels for average predicted yield potential in each environment, and a level 15% below that recommended. In environments where actual rainfall limited yield potential, available N was probably in excess for both high and low treatments. In environments where rainfall exceeded expectations, available N was likely used by the plant for yield enhancement for both N levels. These results reflect the challenges faced by growers that may wish to manage a crop for a particular end use.

Genotypes performed relatively the same across locations and N levels for quality measures. No patterns emerged for interactions, as traits showing interactions were not consistent between the irrigated and moisture-limited trials. The similarity of genotype response across N levels might have arisen because N levels generally did not differ.

Although genotype had a major influence in the performance of grain in a specific end-use quality application, location effects also impacted fundamental properties of a given cultivar (Table 1). Thus, it would be desirable for growers and buyers to have the opportunity to determine the best end-use quality application for a given production lot based on measurable characteristics of the grain. In this regard, we looked at correlations among three grain characteristics that are simple to measure with end-use quality traits that may be ultimately important to grain buyers, and whether these relationships were specific to a given genotype. Bread quality traits were highly related to grain protein, as has been found in numerous studies (Peterson et al., 1992; Lang et al., 1998). For all traits, and especially final loaf volume, higher protein predicted desired changes in bread quality, meaning increased loaf volume, water absorption, dough strength measured by mixograph tolerance, and lower flour ash. On the other hand, higher test weight was associated with undesirable effects on bread quality traits. This presents somewhat of a dichotomy, as greater test weight is generally a positive factor in pricing grain.

Among noodle traits, color characteristics for Chinese noodles were most highly related to any grain characteristic (Table 5). High-protein grain tended to produce noodles with poor initial color and rapid color deterioration after they were manufactured. Alkaline noodle color traits were unrelated to grain protein. This is consistent with previous studies regarding the influence of protein on Chinese noodle color (Lang et al., 1998; Habernicht et al., 2002). Although protein can be an important determinant of color in an alkaline noodle (Miskelly, 1996), the higher pH of the alkaline noodle formula is closer to the optimum for polyphenol oxidase activity (Interesse et al., 1983). A number of studies have shown that polyphenol oxidase activity is related to the degree of time-dependent discoloration of noodles (Kruger et al., 1994; Baik et al., 1995; Park et al., 1997). Therefore, the elevated discoloration due to polyphenol oxidase activity tends to mask protein effects on color to a greater degree in alkali noodles than in Chinese noodles.

The positive effects of grain protein on both bread quality and noodle textural hardness suggests a synergy in management of wheat for both bread and noodle quality. Yet, the detrimental protein effect on noodle color creates an upper limit of acceptable protein concentration in most noodle flours. This suggests that to improve both textural and color components of Asian noodle quality, genotypes or environments that produce either (i) brighter flours against which the effects of the increasing protein concentration are minimized, or (ii) greater quality of protein per unit of protein to produce acceptable hardness values at lower protein concentrations. Selection experiments for components of protein quality such as loaf volume per concentration of protein could be used to verify the degree to which this conclusion can be generalized.

The large influence of genotypes noted may be reflective of the genotypes chosen. They span a wide range of gluten strength and grain protein concentration, and large genotype differences were to be expected. Klasic, Idaho 377s, Lolo, and MTHW9603 were considered dual-purpose wheats, while Hi-Line and the two soft wheats represented the extremes of good bread quality and traditional soft wheat product quality, respectively. A set of genotypes that spanned the range of bread and Asian noodle quality traits seemed appropriate to determine how and when genotypes might bridge across products (bread products vs. Asian noodles) to expand market opportunities. Furthermore, use of wheat in specialty bread products such as European and Chinese steam bread is increasing. Traditional pan bread traits, as measured here, are probably the best indicator of gluten strength and performance in other specialty bread products.

Our results have several implications. First, for the range of environmental conditions we encountered, it is apparent that genotype selection is critical for achieving a desired end use, with location effects being of secondary importance. Second, N management for a particular end use will be difficult, with N level being much less important than cultivar selection and location. Third, grain protein may be the best predictor of the suitability of a particular cultivar produced in a specific year for alternative end-use possibilities, with high-protein grain being most suitable for bread production, and low- and medium-protein, high-quality grain being more suitable for noodle production. And finally, genotypes tended to perform consistently across locations and N levels, and had a consistent relationship of grain traits with bread and noodle traits.

Received for publication February 25, 2003.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 




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E. J. Souza, M. J. Guttieri, K. M. O'Brien, and R. S. Zemetra
Registration of 'UI Darwin' Wheat
Journal of Plant Registrations, January 1, 2008; 2(1): 43 - 46.
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M. J. Guttieri, R. McLean, J. C. Stark, and E. Souza
Managing Irrigation and Nitrogen Fertility of Hard Spring Wheats for Optimum Bread and Noodle Quality
Crop Sci., August 26, 2005; 45(5): 2049 - 2059.
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J. M. Martin, J. E. Berg, A. M. Fischer, A. K. Jukanti, K. D. Kephart, G. D. Kushnak, D. Nash, and P. L. Bruckner
Divergent Selection for Polyphenol Oxidase and Its Influence on Agronomic, Milling, Bread, and Chinese Raw Noodle Quality Traits
Crop Sci., January 1, 2005; 45(1): 85 - 91.
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E.J. Souza, M.J. Guttieri, and J.A. Udall
Registration of 'IDO580' Spring Wheat Germplasm
Crop Sci., January 1, 2005; 45(1): 429 - 430.
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E.J. Souza, M.J. Guttieri, and R. McLean
Registration of 'Gary' Wheat
Crop Sci., July 1, 2004; 44(4): 1476 - 1477.
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E.J. Souza, M.J. Guttieri, K.M. O'Brien, and B. Brown
Registration of 'Alturas' Wheat
Crop Sci., July 1, 2004; 44(4): 1477 - 1478.
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The SCI Journals Agronomy Journal Vadose Zone Journal
Journal of Plant Registrations Soil Science Society of America Journal
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