Root biomass, water-use efficiency, and performance of wheat-rye translocations of chromosomes 1 and 2 in spring bread wheat `Pavon'. (Plant Genetic Resources).
The presence of 1RS.1BL in some hard red winter wheats was associated with higher grain yield, aerial biomass, grain weight, and spikelet fertility (Carver and Rayburn, 1994; Schlegel and Meinel, 1994; Moreno-Sevilla et al., 1995a). However, Moreno-Sevilla et al. (1995b), using a different hard red winter wheat background, reported no yield advantage associated with 1RS.1BL lines. McKendry et al. (1996) reported reduced plant height and delayed heading with the presence of 1RS.1BL, but found no significant yield advantage in soft red winter wheat. Using a set of genetically diverse spring wheat cultivars, Villareal et al. (1991, 1994) found a positive effect of 1RS.1BL on aerial biomass at maturity, spikes per square meter, grain weight, and test weight, but no significant effects on grain yield were detected.
In two sets of 1RS.1BL lines derived from crosses involving `Seri M82', Villareal et al. (1995, 1998) reported higher grain yield, aerial biomass at maturity, grains per spike, grain weight, and test weight associated with 1RS.1BL under optimum and reduced moisture conditions. In these studies, the 1RS.1BL lines delayed flowering and maturity, but had no consistent effect on plant height, harvest index (HI), grains per square meter, and aerial biomass at maturity. Singh et al. (1998) found that the 1RS.1BL translocation in spring bread wheat had a negative effect on grain yield under optimum and droughted conditions.
Another wheat-rye translocation that is commonly used is 1RS.1AL. The 1RS.1AL translocations derived from three winter X spring wheat crosses exhibited increased grain yield, aerial biomass at maturity, spikes per square meter, and test weight under optimum and reduced irrigation conditions compared with their checks (Villareal et al., 1996). These lines showed greater grain weight, delayed maturity, and longer grain filling periods under optimum irrigation. In hard red winter wheat, the presence of 1RS.1AL had no significant effects on grain yield or grain weight (Graybosch et al., 1999). Espitia-Rangel et al. (1999) reported that the 1RS.1AL translocation in winter wheat `Nekota' had a small effect on agronomic performance or environmental stability.
Research on the effect of 1RS.1DL on agronomic performance and end-use quality in bread wheat is limited. The presence of 1RS.1DL in `Gabo' wheat genetic background caused a reduction in grain yield and had a detrimental effect on bread making quality (Koebner and Shepherd, 1988).
The disadvantage of using certain 1RS translocations is that they may reduce the end-use quality of wheat (Dhaliwal et al., 1987; Martin and Stewart, 1990). Graybosch et al. (1993) reported that the 1RS.1AL translocation was less detrimental to dough strength than the 1RS.1BL translocation.
There is evidence that rye has the most highly developed root system among the temperate cereals and it is more tolerant to abiotic stresses such as drought, heat, and cold than bread wheat (Starzycki, 1976). Evaluation of the disomic additions of `Imperial' rye chromosomes to `Chinese Spring' wheat indicated that chromosome 2R increased water-use efficiency and improved rooting characteristics of the recipient wheat cultivar (Lahsaiezadeh et al., 1983; Shah, 1992). The translocation line 2AS.2RL of bread wheat Chinese Spring and Imperial rye surpassed Chinese Spring for grain yield, shoot biomass at maturity, root biomass, and water-use efficiency, especially in droughted conditions (Lahsaiezadeh et al., 1983; Ehdaie et al., 1991, 1998). Furthermore, the long arm of chromosome 2R carries genes for resistance to tan spot [Pyrenophora tritici-repentis (Died.) Drechs.] and Hessian fly [Mayetiola destructor (Say)] (Hatchett et al., 1993; Lee et al., 1996). The 2BS.2RL translocation in bread wheat `Hamlet' was evaluated for bread making quality (Knackstedt et al., 1994). The 2BS.2RL translocation, in contrast to 1RS translocations, did not have a detrimental effect on milling or baking quality of wheat. This translocation showed increased grain yield, aerial biomass at maturity, seeds per spike, and seeds per plant (Fritz and Sears, 1991). However, it delayed maturity and reduced grain weight and HI.
The yield advantage of wheat-rye translocations reported under reduced moisture conditions could be due to their greater water-use efficiency or rooting ability than their nontranslocation counterparts. As far as we are aware, water-use efficiency and rooting ability of wheat-rye translocations have not been studied in translocations involving 1RS, 2RS, and 2RL.
The major objectives of our study were to (i) determine the effect of translocations 1RS.1AL, 1RS.1BL, 1RS.1DL, 2RS.2BL, and 2BS.2RL on root biomass and water-use efficiency when grown in pots under well-watered and droughted conditions and (ii) evaluate field performance of these translocation lines under optimum and terminal drought conditions in the disease-free environment of southern California.
MATERIALS AND METHODS
The original translocation 1RS.1BL of Kavkaz wheat was used to reconstruct the complete chromosome 1R in hexaploid bread wheat Pavon (Lukaszewski, 1993). Then, the reconstructed chromosome 1R was used to develop three new centric translocations 1RS.1AL, 1RS.1BL, and 1RS.1DL in Pavon wheat. Thus, each of these translocations possessed the same rye chromosome arm IRS, which was present in the original translocation 1RS.1BL of Kavkaz wheat and the long arm of chromosome 1 of Pavon wheat (Lukaszewski, 1993).
Centric translocations of chromosome 2R from spring rye cultivar Blanco to chromosome 2B of wheat were produced in the wheat cultivar Chinese Spring by centric breakage-fusion (Lukaszewski, 1993; Brunell et al., 1999) and transferred to Pavon wheat by the backcross procedure. After seven backcrosses, the translocation heterozygotes, which were developed from two separate backcross programs, were self-pollinated. Among their progeny, translocation homozygotes 2RS.2BL and 2BS.2RL and their respective 2B disomic sibs were isolated and grown. All cytological analyses used C-banding for chromosome identification.
The translocation lines involving chromosome 1 and 2 of Pavon (5 lines) along with the 2B disomic sibs, 2B1 and 2B2 (used as checks for 2RS.2BL and 2BS.2RL, respectively), the Kavkaz translocation line (1RS.1BLK), Pavon, and `Yecora Rojo' were used in this study. Seeds of the lines were kindly donated by Dr. A.J. Lukaszewski, University of California, Riverside. Pavon is a spring bread wheat cultivar developed at CIMMYT and recommended for cultivation under irrigated conditions (Calhoun et al., 1994). It is very susceptible to drought, particularly during the grain filling period (Bruckner and Frohberg, 1987). Yecora Rojo is a dwarf, early maturing spring bread wheat cultivar derived from the CIMMYT breeding program and it is still a commercial bread wheat in southern California.
Two separate pot experiments were conducted in an unheated glasshouse at the University of California, Riverside, in 1997 and 1998. One experiment used Pavon and its 1RS translocation lines (1RS.1AL, 1RS.1BL, 1RS.1DL) and the original 1RS.1BLK. The other experiment used Pavon and its 2RS and 2RL translocation lines and their respective checks 2B1 and 2B2. For each experiment, we used a factorial design with 10 treatments (5 genotypes X 2 irrigation regimes), arranged in a randomized complete block design with four replicates.
Seeds from each genotype were soaked in water on 7 Jan. 1997 and on 6 Jan. 1998 for 24 h before being planted into wooden flats. Ten days later, one-leaf seedlings with similar growth were transplanted to plastic pots. Each plastic pot contained a plastic bag filled with 5.0 kg of soil composed of 800 g [kg.sup.-1] sand, 162 g [kg.sup.-1] silt, and 38 g [kg.sup.-1] clay with water-holding capacity of [approximately equal to] 260 g [kg.sup.-1] Each replicate had a similarly treated but unplanted pot to quantify the evaporative water. Each pot was brought to water-holding capacity by adding a predetermined amount of half-strength Hoagland solution (Hoagland and Arnon, 1950) before transplanting a seedling into it. Pots were irrigated with the same solution throughout the study. One day after transplanting the seedlings, 80 g of small-sized perlite was added to the top of each pot to reduce surface evaporation. Pots were weighed every 2 or 3 d and an amount of solution equal to the loss in weight was added.
In the well-watered treatment, hereafter referred to as the wet treatment, pots were irrigated as described until the color of the main tiller of the plants turned yellow. In the droughted treatment, hereafter referred to as the dry treatment, drought was initiated at the early booting stage by adding 33% of solution needed to bring the pots to initial weight. Genotypes received different amounts of solution in both wet and dry treatments due to genotypic differences in days to booting stage and maturity. In the first experiment, booting stage ranged from 67 to 70 d and maturity ranged from 111 to 114 d. In the second experiment, booting stage ranged from 64 to 68 d and maturity ranged from 106 to 112 d. Mean evaporation water calculated from the unplanted pots was from 14.7 to 16.9% in 1997 and from 16.6 to 18.5% in 1998 of total water applied in the experiment. These values overestimate the actual amount of water evaporated from the planted pots.
Plants were harvested at maturity. Shoots were removed from roots at the soil surface. The pots were weighed to the nearest gram, and the soil was carefully washed from the roots. Plant parts were dried at 65[degrees]C for 10 d before weighing. The total amount of water used was calculated as the difference between final and initial pot weight plus the amount of water supplied to each pot (Ehdaie et al., 1991; Ehdaie and Waines, 1993). Thus, the total water used included both transpired and evaporative water. Phenological periods such as days from sowing to early booting, to heading, to anthesis, and to maturity were recorded. Number of tillers and spikes, plant height, root dry matter, shoot dry matter, and total dry matter per plant were measured. Plant water-use efficiency was calculated as grams total dry matter per kilogram water used (Ehdaie, 1995).
Field experiments were planted on 13 Dec. 1999 and on 14 Dec. 2000 in a Ramona Type A sandy loam soil (fine-loamy, mixed, thermic Typic Haploxeralfs) at the Moreno Farm of the University of California Agricultural Experiment Station, Moreno Valley, CA. The nine wheat genotypes used in the glasshouse study, plus Yecora Rojo, were planted in a split-plot design with four replicates (blocks). The main plots consisted of two irrigation treatments, namely well-watered (wet) and droughted (dry) treatments. The split-plots consisted of the genotypes. Plants in the wet treatment were irrigated with sprinklers to minimize water shortage until they reached maturity. Irrigation was terminated for plants in the dry treatment when plants in 50% of plots reached heading stage. In 1999, plants in the wet treatment received 440 mm of water (250.5 mm irrigation + 189.5 mm rain) and those in the dry treatment received 322.5 mm of water (133.0 mm irrigation + 189.5 mm rain). In 2000, plants in the wet treatment received 404 mm of water (225.5 mm irrigation + 181.5 mm rain) and those in the dry treatment received 329.0 mm of water (147.5 mm irrigation + 181.5 mm rain). After irrigation was terminated in the dry treatment, 18.8 mm of rain fell during the grain-filling period in 1999 and 7.3 mm in 2000.
Each plot consisted of six rows, 5.0 m in length. Interrow spacing was 20 cm and interplant spacing was 3 cm. The land was fallowed the previous year and 112.0 kg [ha.sup.-1] urea fertilizer were added to the soil before planting. The two middle rows in each plot were used to harvest 1-m length of plants at maturity to determine shoot biomass and grain yield. Plant height from soil surface to the tip of a spike (excluding awns) was measured from three randomly chosen spots in each plot at maturity. Two 50-cm lengths of two of the middle rows in each plot were used to count the number of tillers and spikes at maturity. Five spikes were randomly chosen from each plot to determine mean number of grains per spike and grain weight. Harvest index was calculated as the ratio of grain yield to shoot biomass. In 2000 only, one 1-m length of plants at anthesis was harvested from the second and fifth rows and immediately were dried in a forced-air drier at 60[degrees]C for 6 d to determine the relationship between shoot biomass at anthesis and grain weight and grain yield at maturity. Days from plant emergence to boot stage, to heading, to anthesis, and to maturity were recorded. Grain filling period was calculated as the difference between days to maturity and days to anthesis.
Analysis of variance was performed for each character measured in the glasshouse experiments and the field experiment for each year (Steel et al., 1997). The combined ANOVA was also performed across years for the glasshouse experiments and for the field experiments. Associations among characters were examined by correlation analysis. The key comparisons in our study were between Pavon and each of 1RS.1AL, 1RS.1BL, and 1RS.1DL translocations, between 2RS.2BL and its check 2B1, between 2BS.2RL and its check 2B2, and between 1RS.1BL and 1RS.1BLK. Mean comparisons between Pavon and its 1RS translocations used Dunnett's test (control vs. treatments) and other comparisons utilized the LSD test (Steel et al., 1997).
A stress tolerance index (STI) was used to characterize relative response of each genotype to stressed field conditions (Fernandez, 1992). The index was calculated from genotype means using the generalized formula
STI = [([Y.sub.P]/[[bar]Y.sub.P])([Y.sub.S]/ [[bar]Y.sub.S])([[bar]Y.sub.S]/[[bar]Y.sub.P]) = ([Y.sub.P])([Y.sub.S])/([[bar]Y.sub.P]).sup.2]
where [Y.sub.P] and [Y.sub.S] are the yield of a given genotype in a nonstress (yield potential) and stress environment, respectively, and [[bar]Y.sub.P] and [[bar]Y.sub.S] are mean yield in nonstress and stress environment, respectively. Therefore, STI is a function of relative performance of a genotype in nonstress ([Y.sub.P]/[Y.sub.P]), and stress ([Y.sub.S]/[Y.sub.S]) environments and the stress intensity ([Y.sub.S]/[Y.sub.P]). Greater values of STI for a genotype indicate greater stress tolerance and yield potential.
RESULTS AND DISCUSSION
The combined ANOVA (not shown) indicated highly significant main effects for year, irrigation, and genotype for most of the characters examined. The genotype X year interaction was highly significant for days to maturity, root dry matter, and grain weight for Pavon and its 1RS translocation lines in the first experiment and for most of the characters examined for Pavon and its 2B translocation lines and their checks in the second experiment. However, the significant genotype X year interactions observed were almost entirely due to differences in changes in magnitude of the means rather than in ranking of the genotypes in different years. Therefore, means averaged across years are reported.
Mean values for Pavon and its 1RS translocation lines under wet and dry treatments are presented in Table 1. Experimental precision was good as indicated by the small to intermediate coefficients of variation for all the measured characters (Table 1). Pavon and its 1RS translocation lines were similar in plant maturity under both treatments (Table 1). The 1RS translocations showed a negative trend for plant height, but a positive trend for number of tillers and spikes per plant. A strong positive trend was shown by the 1RS translocations for root production (Table 1). Root dry matter increased significantly in 1RS.1AL and 1RS.1DL in well-watered and only in 1RS.1AL in droughted conditions. The relative increases in root dry matter in 1RS translocations were consistent in both treatments. Roots in the 1RS translocation lines were more branched and narrower than those in Pavon. Increase in root dry matter in the 1RS translocations did not have a depressing effect on shoot dry matter or grain yield (Table 1). In fact, the 1RS translocations showed a positive trend for total dry matter. The 1RS translocations also exhibited a positive trend for total water used. Since days to maturity were similar for Pavon and its 1RS translocations, it appears that the 1RS translocations had increased transpiration rates by using more water and producing more dry matter per day than Pavon. Total dry matter produced is positively and linearly correlated to total water used (Hubick et al., 1986; Ismail and Hall, 1992; Ehdaie, 1995). The presence of 1RS translocations in the background of Pavon had no significant effects on grain yield, number of grains per plant, grain weight, and water-use efficiency (WUE; Table 1).
Mean values of Pavon and its 1R translocation lines (1RS.1AL, 1RS.1BL, 1RS.1DL) in both years (n = 8) were used to determine the association between root biomass and grain yield under well-watered and under droughted conditions. The correlation coefficients between root biomass and grain yield was significant under droughted (r = 0.89, P < 0.01) and under well-watered conditions (r = 0.66, P < 0.07).
The presence of 2RS.2BL in the Pavon background, in general, delayed maturity and increased the number of tillers per plant (Table 2). Under well-watered conditions, number of spikes per plant increased, whereas grain weight decreased in the presence of 2RS.2BL. Grain yield, number of grains per plant, and grain weight exhibited negative trends in the presence of the 2RS.2BL translocation (Table 2). The short arm of chromosome 2 of rye, 2RS, is partially homeologous to the short arms of both group 2 and 6 chromosomes of wheat (Naranjo et al., 1987; Devos et al., 1993). Therefore, 2RS is not capable of fully compensating for the absence of 2BS (Brunell et al., 1999) and a reduction in plant performance is expected in 2RS.2BL translocations as reported by Gupta et al. (1989) and also confirmed by our observations.
The presence of 2BS.2RL in the Pavon background had little effect on most characters examined (Table 2). However, it significantly delayed maturity and reduced plant height under well-watered conditions. A positive trend for number of grains per plant was observed in the presence of 2BS.2RL. The negative effect of 2BS.2RL translocation on grain weight was significant and consistent across the irrigation treatments (Table 2). The presence of the 2RS.2BL or 2BS.2RL translocation in Pavon had no significant effect on WUE. Experimental precision was satisfactory as indicated by the small to moderate coefficients of variation for most characters examined, except root dry matter (Table 2).
The results obtained from the pot experiments for the two reciprocal centric translocations 2RS.2BL and 2BS.2RL were unexpected. Since the long arm of chromosome 2 of rye, 2RL, is homeologous to 2BL (Brunell et al., 1999), the presence of 2BS.2RL translocation was expected to have more positive and less negative effects on plant performance than those of the 2RS.2BL translocation. However, such a trend was not observed (Table 2).
The combined ANOVA (not shown) indicated highly significant main effects for year, irrigation, and genotype for most of the characters examined. The year X irrigation, genotype X year, genotype X irrigation, and genotype X year X irrigation interactions were significant or highly significant for most of the characters examined. The genotype X year interactions were mainly due to changes in the magnitude rather than ranking of the genotypic means in different years. Thus, means averaged across years are reported.
Experimental precision was high as indicated by the small coefficients of variation for all the measured characters, except for grain yield (Table 3). The presence of 1RS in the Pavon background delayed maturity by 3 d under wet and dry field conditions (Table 3), which was in agreement with other reports (Carver and Rayburn, 1994; Villareal et al., 1995, 1996, 1998; Singh et al., 1998). Compared with Pavon, grain filling period was longer in 1RS.1AL by 7 d and in 1RS.1BL by 5 d under wet field conditions and in 1RS.1AL by 4 d under dry field conditions (Table 3). The presence of the 1RS.1DL in Pavon reduced plant height significantly. The presence of 1RS translocations in Pavon background significantly increased shoot biomass by 13% only under wet field conditions (Table 3). Also, grain weight and grain yield of the 1RS translocations increased by 15.7 and 27.6%, respectively, under wet field conditions compared with those of Pavon (Table 3). Pavon and its 1RS translocations were similar for number of spikes per 50 cm, number of grains per spike, and HI, except for 1RS.1AL translocation that had more spikes and higher HI than Pavon under wet field conditions (Table 3). The superior performance of the 1RS translocations over Pavon in grain production under wet field conditions appeared to be mainly due to their heavier grains. Villareal et al. (1996) also reported a longer grain filling period and heavier grains for different 1RS.1AL translocations compared with their respective checks. Grain yield of the 1RS translocations also were greater than that of the commercial check Yecora Rojo under well-watered field conditions (Table 3).
The 2RS.2BL translocation in the Pavon background had no beneficial effect on any of the characters examined (Table 3). The presence of the 2BS.2RL translocation reduced number of spikes per 50 cm under both irrigation regimes, delayed maturity by 3 d and increased number of grains per spike under wet conditions, and reduced grain filling period by 5 d in dry conditions (Table 3). Fritz and Sears (1991) also reported that presence of a 2BS.2RL translocation in `Karl' wheat background delayed maturity and increased number of grains per spike. They also reported reduced HI and grain weight and increased grain yield for the 2BS.2RL translocation, which were not observed in our study. These conflicting observations indicate that the effect of different 2BS.2RL translocations on agronomic performance depends on the genetic background of the recipient wheat cultivar and their interactions with the genes carried by the 2RL segment of a specific rye cultivar, which was also reported for 1RS.1BL translocations (Carver and Rayburn, 1994; McKendry et al., 1996; Singh et al., 1998). The performance of the 2B1 and 2B2 checks was expected to be similar to that of Pavon. However, the 2B2 check showed higher grain yield and HI and produced more spikes and grains per spike than Pavon under wet field conditions (Table 3). Since 2B2 was developed in a backcrossing program, it appears that more backcrossing to recurrent parent Pavon was needed to recover most of Pavon genetic background.
The correlation coefficients between shoot biomass at anthesis and grain weight and grain yield calculated only in 2000 season were not significant, indicating that preanthesis assimilates were not a major source in determining grain yield in that season (Ehdaie and Waines, 1996).
The STI measured for the genotypes based on grain yield and kernel weight are presented in Table 4. The growing season was longer in 2000 than in 1999. The grain filling period in 2000 coincided with partly cloudy days and less heat. Therefore, environmental stresses were less in 2000 than in 1999. On average, drought significantly (P < 0.01) reduced grain yield by 68% and kernel weight by 30% in 1999. In 2000, the two traits also were significantly (P < 0.01) reduced under droughted field conditions by 38 and 34%, respectively. The grain yield-based STI and kernel weight-based STI are measures of relative overall and postanthesis stress tolerance, respectively (Bruckner and Frohberg, 1987). Pavon had consistently low STI, confirming previous reports that this cultivar was susceptible to drought (Calhoun et al., 1994; Bruckner and Frohberg, 1987). The STI values for Yecora Rojo were relatively low, except for grain weight-based STI in the 2000 growing season. The original translocation 1RS.1BL in Kavkaz wheat showed consistent and relatively moderate values for STI (Table 4). In contrast, the STI values for translocation 1RS.1BL in Pavon wheat were not consistent across both years. Since both 1RS.1BL translocations in our study used the same 1RS rye segment, it appears that enhanced adaptability reported for certain 1RS.1BL translocations is the result of complex gene interactions between genes in the iRS rye chromosome and genes of the recipient wheat cultivar. In the more stressful environments of 1999, the 1RS.1DL and 1RS.1BL translocations exhibited, respectively, greater overall and postanthesis tolerance to drought than Pavon (Table 4). In the less stressful environments of 2000, the overall tolerance of 1RS.1BL and 1RS.1AL translocations and postanthesis tolerance of 1RS.1DL translocation were greater than those of Pavon. The 2RS.2BL and 2BS.2RL translocations had lower values for STI compared with their respective checks (Table 4), indicating that these Blanco rye translocations in Pavon wheat were not beneficial for either yield potential or tolerance to stress environments. In contrast to the 2BS.2RL translocation in the present study, the 2AS.2RL translocation in our previous studies (Lahsaiezadeh et al., 1983; Ehdaie et al., 1991, 1998) showed positive effects on WUE and on field performance, although different bread wheat and rye cultivars (Chinese Spring wheat and Imperial rye) were used to develop these translocations.
Although the results obtained in the glasshouse and field experiments indicated that 1RS translocations in the Pavon background delayed maturity and reduced plant height, they exhibited positive effects on grain yield and grain weight under well-watered conditions. The relatively higher values of STI observed for the 1RS translocations compared with Pavon in disease-free southern California were mainly due to their greater grain yield potential. The consistent tendency of the 1RS.1A1, 1RS.1BL, and 1RS.1DL translocations to produce more root biomass, as evidenced in the glasshouse experiments, might have contributed to their overall greater grain production under field conditions as compared with Pavon wheat. Root biomass, averaged across the irrigation treatments and years, was 2.7 g [plant.sup.-1] for Pavon, 3.5 g [plant.sup.-1] for 1RS.1AL, 3.0 g plant-t for 1RS.1BL, and 3.4 g [plant.sup.-1] for 1RS.1DL translocations. A larger root biomass will enhance water and nutrient uptake, which may contribute to increased yield. The overall mean grain yield produced under field conditions was 4.066 Mg [ha.sup.-1] for Pavon, 4.895 Mg [ha.sup.-1] for 1RS.1AL, 4.503 Mg [ha.sup.-1] for 1RS.1BL, and 4.633 Mg [ha.sup.-1] for 1RS.1DL translocations. The 7% higher overall mean grain yield of the 1RS.1BL translocation observed in our study is comparable with those reported earlier (Carver and Rayburn, 1994; Moreno-Sevilla et al., 1995a,b). The 20% higher overall mean grain yield observed for the 1RS.1AL translocation is greater than the 3 to 4% reported by Villareal et al. (1996). This difference could be due to the genetic background effects of the wheat and rye cultivars used to produce the translocations, which were also detected for the 1RS.1BL translocations (Rajaram and van Ginkel, 1996). In our study, the 1RS.1DL translocation exhibited 14% higher overall mean grain yield compared with Pavon wheat. These results may serve to encourage the development and use of the 1RS.1AL and 1RS.1DL translocations in wheat breeding programs, although increased grain yield may not be associated with increased water-use efficiency.
The CIMMYT-derived wheats such as Yecora Rojo and Pavon in the present study and `Anza' and `Chenab 70' in our previous study (Ehdaie et al., 1991) showed relatively small root biomass compared with some landrace wheats. This may be a general phenomenon of some CIMMYT-derived wheats selected under high irrigation and fertilizer inputs. It may be possible to increase grain yield in CIMMYT-type wheats by also selecting for a larger root system. Root biomass is under genetic control with a relatively high heritability under both well-watered and droughted conditions (Ehdaie et al., 2001). A wheat ideotype should react positively to drought by producing a larger root biomass under droughted compared with favorable conditions. The translocation lines examined here did not exhibit this root response. It appeared that presence of the 1RS translocation in the genetic background of Pavon enhanced root biomass only under well-watered conditions. The increased yield potential of certain 1RS.1BL translocations reported in the literature (Rajaram et al., 1983; Villareal et al., 1991, 1995; Moreno-Sevilla et al., 1995a) may be due to their greater root biomass and the observed higher transpiration rate. The promising yield performance reported for the 1RSK translocations in Pavon suggest that additional translocations involving the other rye chromosomes should be systematically developed and tested in a common wheat background in gravimetric pot and field studies.
Table 1. Means per plant, averaged across years, for bread wheat `Pavon' and its 1RS translocation lines, and changes relative to Pavon (%) under well-watered and droughted pot conditions. Well-watered Character Pavon 1RS.1AL 1RS.1BL 1RS.1DL Days to maturity 114 115 (1) 114 (0) 115 (1) Plant height, cm 90 92 (2) 88 (-2) 88 (-2) No. of tillers 6.6 7.8 (18) * 7.4 (12) 8.6 (15) No. of spikes 5.3 5.9 (11) 5.6 (6) 5.3 (0) Root dry matter, g 2.5 3.4 (36) * 3.0 (20) 3.4 (36) * Shoot dry matter, g 32.1 35.4 (10) 34.8 (8) 33.5 (4) Total dry matter, g 34.6 38.7 (12) 37.9 (10) 36.9 (7) Total water used, kg 12.2 13.5 (11) * 13.1 (7) 12.7 (4) Grain yield, g 15.9 17.5 (10) 16.7 (5) 15.6 (-2) Number of grains 320 359 (12) 339 (6) 322 (1) Grain weight, mg 51.4 50.7 (-1) 50.7 (-1) 50.6 (-2) WUE, g [kg.sup.-1] ([dagger]) 2.9 2.9 (0) 2.9 (0) 2.9 (0) Droughted Character Pavon 1RS.1AL 1RS.1BL 1RS.1DL Days to maturity 111 113 (2) 111 (0) 113 (2) Plant height, cm 89 85 (-5) 83 (-7) * 86 (-3) No. of fillers 6.0 7.0 (17) 6.0 (0) 7.0 (17) No. of spikes 4.0 5.0 (25) * 4.0 (0) 5.0 (25) * Root dry matter, g 2.9 3.6 (24) * 3.0 (3) 3.3 (14) Shoot dry matter, g 25.6 28.2 (10) 26.3 (3) 26.4 (3) Total dry matter, g 28.5 31.8 (12) 29.3 (3) 29.7 (4) Total water used, kg 9.0 9.9 (10) 9.3 (3) 9.5 (6) Grain yield, g 12.3 13.2 (7) 12.3 (0) 11.6 (-6) Number of grains 246 263 (7) 244 (-1) 240 (-2) Grain weight, mg 51.2 50.9 (-1) 51.1 (0) 49.8 (-3) WUE, g [kg.sup.-1] ([dagger]) 3.1 3.2 (3) 3.2 (3) 3.1 (0) Character CV % Days to maturity 2.1 Plant height, cm 4.1 No. of fillers 14.3 No. of spikes 14.4 Root dry matter, g 15.1 Shoot dry matter, g 11.0 Total dry matter, g 10.7 Total water used, kg 7.4 Grain yield, g 11.8 Number of grains 14.0 Grain weight, mg 3.2 WUE, g [kg.sup.-1] ([dagger]) 5.2 * Significant at the P = 0.05 probability level according to Dunnett's test. ([dagger]) WUE=water-use efficiency (total dry matter/total water used). Table 2. Means per plant, averaged across years, for 2RS.2BL and 2BS.2RL translocation lines of bread wheat `Pavon' and changes relative to their respective checks 2B1 and 2B2 (%) under well-watered and droughted pot conditions. Well-watered Droughted Character 2B1 2RS.2BL 2B1 2RS.2BL Days to maturity 110 113 (3) * 107 111 (4) * Plant height, cm 92 88 (-4) 89 88 (-1) Number of tillers 6 8 (13) * 5 7 (40) * Number of spikes 5 7 (40) * 4 4 (0) Root dry matter, g 2.8 2.8 (0) 2.4 2.6 (8) Shoot dry matter, g 31.2 33.5 (7) 22.8 23.3 (2) Total dry matter, g 34 36.3 (7) 25.2 25.9 (3) Total water used, kg 11.7 12.9 (10) 8.5 9.0 (6) Grain yield, g 16.4 15.0 (-9) 11.7 10.0 (-15) Number of grains 325 318 (-2) 220 195 (-11) Grain weight, mg 50.1 47.6 (-5) * 53.5 51.6 (-4) WUE, g [kg.sup.-1] ([dagger]) 2.8 2.9 (4) 3.0 2.9 (-3) Well-watered Droughted Character 2B2 2BS.2RL 2B2 2BS.2RL Days to maturity 106 109 (3) * 105 106 (1) Plant height, cm 90 83 (-8) * 85 82 (-4) Number of tillers 6 5 (-17) 5 4 (-20) * Number of spikes 5 5 (0) 4 4 (0) Root dry matter, g 2.3 2.0 (-13) 2.3 2.5 (9) Shoot dry matter, g 29.0 27.4 (-6) 23.3 23.3 (0) Total dry matter, g 31.2 29.4 (-6) 25.6 25.7 (0) Total water used, kg 10.8 10.8 (0) 8.5 8.6 (1) Grain yield, g 15.4 14.6 (-5) 12.0 12.1 (1) Number of grains 301 341 (13) 237 269 (14) Grain weight, mg 51.5 42.9 (-17) * 51.2 44.8 (-13) * WUE, g [kg.sup.-1] ([dagger]) 2.9 2.8 (-3) 3.0 3.0 (0) Character CV % Days to maturity 2.4 Plant height, cm 4.9 Number of tillers 17.0 Number of spikes 16.1 Root dry matter, g 20.9 Shoot dry matter, g 15.6 Total dry matter, g 15.6 Total water used, kg 13.0 Grain yield, g 15.2 Number of grains 16.3 Grain weight, mg 4.1 WUE, g [kg.sup.-1] ([dagger]) 5.7 * Significant at the P = 0.05 probability level according to LSD test. ([dagger]) WUE = water-use efficiency (total dry matter/total water used). Table 3. Means, averaged across years, for bread wheat `Pavon' and its 1RS and 2RS.2BL and 2BS.2RL transiocation lines and their respective checks 2B1 and 2B2 along with the 1RS.1B[L.sub.K] (`Kavkaz' wheat), and `Yecora Rojo' under well-watered (wet) and droughted (dry) field conditions. Days to Grain-filling maturity period Plant height Genotype Wet Dry Wet Dry Wet Dry d cm Pavon 157c 151c 40d 36c 81a 72a ([dagger]) 1RS.1AL 161a 154ab 47b 40b 78ab 71ab 1RS.1BL 161a 153b 45bc 37c 75bc 68abc 1RS.1DL 159b 155a 41d 36c 73c 67bc 1RS.1B [L.sub.K] 159b 151c 44c 38bc 78ab 70abc 2RS.2BL 162a 154ab 45bc 36c 75bc 69abc 2B1 159b 154ab 44c 40b 78ab 70abc 2BS.2RL 162a 153b 44c 34d 80a 72a 2B2 159b 154ab 44c 39b 78ab 70abc Yecora Rojo 143d 147d 49a 44a 64d 59d CV, % 0.8 5.3 6.3 No. of No. of grains Shoot biomass spikes per spike Genotype Wet Dry Wet Dry Wet Dry Mg [ha.sup.-1] Pavon 13.8bc 10.1abc 47cd 45a 43cd 43b 1RS.1AL 15.5a 10.1abc 57a 42ab 39d 42bc 1RS.1BL 15.9a 9.1c 51bc 39b 42cd 38cd 1RS.1DL 15.5a 9.7bc 50bc 43ab 46bc 42bc 1RS.1B [L.sub.K] 14.4ab 10.1abc 54ab 45a 39d 38cd 2RS.2BL 14.4ab 9.1c 54ab 44ab 39d 35de 2B1 13.6bc 9.2bc 53ab 42ab 43cd 43b 2BS.2RL 14.4ab 9.5bc 42d 31c 52a 53a 2B2 14.7ab 10.6ab 52ab 44ab 48b 49a Yecora Rojo 12.6c 9.5bc 57a 44ab 34e 33e CV, % 12.4 11.2 10.0 Harvest Grain weight index Grain field Genotype Wet Dry Wet Dry Wet Dry mg % Mg [ha.sup.-1] Pavon 36ef 27cde 39d 28abc 5.2de 2.9ab 1RS.1AL 41bcd 27cde 45a 27abc 7.0a 2.8ab 1RS.1BL 42bc 29bcd 40cd 25c 6.5ab 2.4b 1RS.1DL 42bc 26def 41cd 29ab 6.4abc 2.9ab 1RS.1BLK 44ab 29bcd 43ab 28abc 6.2bc 2.9ab 2RS.2BL 43bc 31bc 39d 29ab 5.7cde 2.7ab 2B1 39cde 26def 43ab 27abc 6.0bcd 2.6ab 2BS.2RL 35f 23f 42abc 27abc 6.0bcd 2.7ab 2B2 38def 25ef 45a 30ab 6.6b 3.2a Yecora Rojo 44ab 35a 39d 31a 5.0e 3.1ab CV, % 11.5 10.6 17.6 ([dagger]) Means followed by the same letter within a column are not significantly different at the P = 0.05 probability level according to LSD test. Table 4. Stress tolerance indices (STI) ([dagger]) based on grain yield and kernel weight for bread wheat `Pavon', its 1RS, 2RS.2BL and 2BS.2RL translocation lines and their respective checks 2B1 and 2B2, along with the 1RS.1B[L.sub.K] (`Kavkaz' wheat), and `Yecora Rojo' in 1999 and 2000. STI in 1999 Genotype Grain yield Kernel weight von 0.25 [+ or -] 0.04 0.61 [+ or -] 0.09 ([double dagger]) 1RS.1AL 0.31 [+ or -] 0.07 0.75 [+ or -] 0.09 1RS.1BL 0.18 [+ or -] 0.02 0.83 [+ or -] 0.03 1RS.1DL 0.42 [+ or -] 0.04 0.63 [+ or -] 0.09 1RS.1B[L.sub.K] 0.35 [+ or -] 0.03 0.84 [+ or -] 0.05 2RS.2BL 0.29 [+ or -] 0.06 0.82 [+ or -] 0.05 2B1 0.28 [+ or -] 0.05 0.72 [+ or -] 0.08 2BS.2RL 0.29 [+ or -] 0.07 0.49 [+ or -] 0.05 2B2 0.58 [+ or -] 0.07 0.64 [+ or -] 0.03 Yecora Rojo 0.29 [+ or -] 0.06 0.60 [+ or -] 0.05 STI in 2000 Genotype Grain yield Kernel weight von 0.57 [+ or -] 0.04 0.58 [+ or -] 0.05 1RS.1AL 0.80 [+ or -] 0.05 0.58 [+ or -] 0.05 1RS.1BL 0.75 [+ or -] 0.06 0.61 [+ or -] 0.03 1RS.1DL 0.58 [+ or -] 0.05 0.65 [+ or -] 0.04 1RS.1B[L.sub.K] 0.59 [+ or -] 0.06 0.64 [+ or -] 0.05 2RS.2BL 0.51 [+ or -] 0.11 0.73 [+ or -] 0.06 2B1 0.54 [+ or -] 0.06 0.51 [+ or -] 0.03 2BS.2RL 0.58 [+ or -] 0.09 0.46 [+ or -] 0.05 2B2 0.58 [+ or -] 0.04 0.45 [+ or -] 0.05 Yecora Rojo 0.40 [+ or -] 0.07 1.31 [+ or -] 0.09 ([dagger]) STI = ([Y.sub.P]/[[bar]Y.sub.P])([[bar]Y.sub.S]/[[bar] Y.sub.S])([bar]Y.sub.S]/[[bar]Y.sub.P]) = ([Y.sub.P])([Y.sub.S])/ [([[bar]Y.sub.P]).sup.2], where [Y.sub.P] and [Y.sub.S] are the yield of a given genotype in well-watered (yield potential) and droughted treatment; [[bar]Y.sub.P], and [[bar]Y.sub.S] are mean yield in well-watered and droughted treatment, respectively. ([double dagger]) Mean [+ or -] SE of the mean.
Research supported in part by grant number SWC-96N01/ 97R01 from the Southwest Consortium on Plant Genetics and Water Resources to Drs. Lukaszewski, Whitkus, and Ehdaie, the California Agricultural Experiment Station, and the University of California, Riverside, Botanic Gardens.
Bruckner, P.L., and R.C. Frohberg. 1987. Stress tolerance and adaptation in spring wheat. Crop Sci. 27:31-36.
Brunell, M.S., A.J. Lukaszewski, and R. Whitkus. 1999. Development of arm specific RAPD markers for rye chromosome 2R in wheat. Crop Sci. 39:1702-1706.
Calhoun, D.S., G. Gebeyehu, A. Miranda, S. Rajaram, and M. van Ginkel. 1994. Choosing evaluation environments to increase wheat grain yield under drought conditions. Crop Sci. 34:673-678.
Carver, B.F., and A.L. Rayburn. 1994. Comparison of related wheat stocks possessing 1B or 1RS.1BL chromosomes: Agronomic performance. Crop Sci. 34:1505-1510.
Devos, K.M., M.D. Atkinson, C.N. Chinoyt, H.A. Francis, R.L. Hartcourt, R.M.D. Koebner, C.J. Liu, P. Masojc, D.X. Xie, and M.D. Gale. 1993. Chromosomal rearrangements in rye genome relative to that of wheat. Theor. Appl. Genet. 85:673-680.
Dhaliwal, A.S., D.J. Mares, and D.R. Marshall. 1987. Effect of 1B/ 1R chromosome translocation on milling and quality characteristics of bread wheats. Cereal Chem. 64:72-76.
Ehdaie, B. 1995. Variation in water-use efficiency and its components in wheat: II. Pot and field experiments. Crop Sci. 35:1617-1626.
Ehdaie, B., D. Barnhart, and J.G. Waines. 1998. Effects of the 2AS.2RL translocation on grain yield and evapotranspiration efficiency of `Chinese Spring' bread wheat, p. 38-39. In A.E. Slinkard (ed.) Proc. Int. Wheat Genet. Symp., 9th, Saskatoon, SK, Canada. Vol. 2. 2-7 Aug. 1998. Univ. of Saskatchewan, Saskatoon, SK, Canada.
Ehdaie, B., D. Barnhart, and J.G. Waines. 2001. Inheritance of root and shoot biomass in a bread wheat cross. J. Genet. Breed. 55:1-10.
Ehdaie, B., A.E. Hall, G.D. Farquhar, H.T. Nguyen, and J.G. Waines. 1991. Water-use efficiency and carbon isotope discrimination in wheat. Crop Sci. 31:1282-1288.
Ehdaie, B., and J.G. Waines. 1993. Variation in water-use efficiency and its components in wheat: I. Well-watered pot experiment. Crop Sci. 33:294-299.
Ehdaie, B., and J.G. Waines. 1996. Genetic variation for contribution of preanthesis assimilates to grain yield in spring wheat. J. Genet. Breed. 50:47-56.
Espitia-Rangel, E., P.S. Baenziger, R.A. Graybosch, D.R. Shelton, B. Moreno-Sevilla, and C.J. Peterson. 1999. Agronomic performance and stability of 1A vs. 1AL.1RS genotypes derived from winter wheat `Nekota'. Crop Sci. 39:643-648.
Fernandez, G.C.J. 1992. Effective selection criteria for assessing plant stress tolerance, p. 257-270. In C.G. Kuo (ed.) Adaptation of food crops to temperature and water stress, p. 531. In Proc. Int. Symp., Taipei, Taiwan. 13-18 Aug. 1992. Publ. no. 93-410. Asian Vegetable Res. and Dev. Center, Shanhua, Taiwan.
Fritz, A.K., and R.G. Sears. 1991. The effect of the Hamlet (2BS.2RL) translocation on yield components of hard red winter wheat, p. 94. In 1991 Agronomy abstracts. ASA, Madison, WI.
Graybosch, R.A., J.H. Lee, C.J. Peterson, D.R. Porter, and O.K. Chung. 1999. Genetic, agronomic and quality comparisons of two 1AL.1RS wheat-rye chromosomal translocations. Plant Breed. 118: 125-130.
Graybosch, R.A., C.J. Peterson, L.E. Hansen, D. Worrall, D.R. Shelton, and A. Lukaszewski. 1993. Comparative flour quality and protein characteristics of 1BL/1RS and 1AL/1RS wheat-rye translocation lines. J. Cereal Sci. 17:95-106.
Gupta, R.B., K.W. Shepherd, and F. MacRitchie. 1989. Effect of rye chromosome arm 2RS on flour proteins and physical dough properties in bread wheat. J. Cereal Sci. 10:169-174.
Hatchett, J.H., R.G. Sears, and T.S. Cox. 1993. Inheritance of resistance to Hessian fly in rye and in wheat-rye translocation lines. Crop Sci. 33:730-734.
Heun, M., and G. Fishbeck. 1987. Identification of wheat powdery mildew resistance genes by analyzing host-pathogen interactions. Plant Breed. 98:124-129.
Hubick, K.T., G.D. Farquhar, and R. Shorter. 1986. Correlation between water-use efficiency and carbon isotope discrimination in diverse peanut (Arachis) germplasms. Aust. J. Plant Physiol. 13:803-816.
Hoagland, D.R., and D.I. Arnon. 1950. The water-culture method for growing plants without soil. Circ. 347. California Agric. Exp. Stn., Berkeley, CA.
Ismail, A.M., and A.E. Hall. 1992. Correlation between water-use efficiency and carbon isotope discrimination in diverse cowpea genotypes and isogenic lines. Crop Sci. 32:7-12.
Knackstedt, M.A., R.G. Sears, D.E. Rogers, and G.L. Lookhart. 1994. Effects of T2BS.2RL wheat-rye translocation on breadmaking quality in wheat. Crop Sci. 34:1066-1070.
Koebner, R.M.D., and K.W. Shepherd. 1988. Isolation and agronomic assessment of allosyndetic recombinants derived from wheat/rye translocation 1DL.1RS, carrying reduced amounts of rye chromatin. p. 343-348. In T.E. Miller and R.M.D. Koebner (ed.) Proc. Int. Wheat Genet. Symp., 7th, Cambridge, England. 13-19 July 1988. Inst. of Plant Science Res., Cambridge.
Lahsaiezadeh, M., I.P. Ting, and J.G. Waines. 1983. Drought resistance in Chinese Spring wheat/Imperial rye addition and substitution lines, p. 945-950. In S. Sakamoto (ed.) Proc. Int. Wheat Genet. Symp., 6th, Kyoto, Japan. 28 Nov.-3 Dec. 1983. Plant Germplasm Inst., Kyoto Univ., Kyoto, Japan.
Lee, J.H., R.A. Graybosch, S.M. Kaeppler, and R.G. Sears. 1996. A PCR assay for detection of a 2RL.2BS wheat-rye chromosome translocation. Genome 39:605-608.
Lukaszewski, A.J. 1990. Frequency of 1RS.1AL and 1RS.1BL translocations in United States wheats. Crop Sci. 30:1151-1153.
Lukaszewski, A.J. 1993. Reconstruction in wheat of complete chromosomes 1B and 1R from the 1RS.1BL translocation of `Kavkaz' origin. Genome 36:821-824.
Martin, D.J., and B.G. Stewart. 1990. Dough stickiness in rye-derived wheat cultivars. Euphytica 51:77-86.
McIntosh, R.A. 1983. A catalogue of gene symbols for wheat, p. 1197-1255. In S. Sakamoto (ed.) Proc. Int. Wheat Genet. Symp., 6th, Kyoto, Japan. 28 Nov.-3 Dec. 1983, Plant Germplasm Inst., Kyoto Univ., Kyoto, Japan.
McKendry, A.L., D.N. Tague, P.L. Finny, and K.E. Miskin. 1996. Effect of 1BL. 1RS on milling and baking quality of soft red winter wheat. Crop Sci. 36:848-851.
Merker, A. 1982. `Veery'--A CIMMYT spring wheat with 1B/1R chromosome translocation. Cereal Res. Commun. 10:105-106.
Moreno-Sevilla, B., P.S. Baenziger, C.J. Peterson, R.A. Graybosch, and D.V. McVey. 1995a. The 1BL.1RS translocation: Agronomic performance of [F.sub.3]-derived lines from a winter wheat cross. Crop Sci. 35:1051-1055.
Moreno-Sevilla, B., P.S. Baenziger, D.R. Shelton, R.A. Graybosch, and C.J. Peterson. 1995b. Agronomic performance and end-use quality of 1B vs. 1BL/1RS genotypes derived from winter wheat `Rawhide'. Crop Sci. 35:1607-1612.
Naranjo, T., A. Rocca, P.G. Goiocoechea, and R. Giraldez. 1987. Arm homoeology of wheat and rye chromosomes. Genome 29:873-882.
Rajaram, S., Ch.E. Mann, G. Ortiz-Ferrara, and A. Mujeeb-Kazi. 1983. Adaptation, stability and high yield potential of certain 1B/ 1R CIMMYT wheats, p. 613-621. In S. Sakamoto (ed.) Proc. Int. Wheat Genet. Symp., 6th, Kyoto, Japan. 28 Nov.-3 Dec. 1983. Plant Germplasm Inst., Kyoto Univ., Kyoto, Japan.
Rajaram, S., and M. van Ginkel. 1996. Yield potential debate: Germ plasm vs. methodology, or both. p. 11-18. In M.P. Reynolds et al. (ed.) Increasing yield potential in wheat: Breaking the barriers. Proc. of a Workshop. March 1996. Ciudad Obregon, Sonora, Mexico.
Rajaram, S., R.L. Villareal, and A. Mujeeb-Kazi. 1990. The global impact of 1B/1R spring wheat, p. 105. In 1990 Agronomy abstracts. ASA, Madison, WI.
Schlegel, R., and A. Meinel. 1994. A quantitative trait locus (QTL) on chromosome arm 1RS rye and its effect on yield performance of hexaploid wheat. Cereal Res. Commun. 22:7-13.
Shah, S.H. 1992. Drought resistance in wheat relatives and their addition lines. Ph.D. diss. Univ. of California, Riverside, CA (Diss. Abstr. AAG9231945).
Singh, R.P., J. Huerta-Espino, S. Rajaram, and J. Crossa. 1998. Agronomic effects from chromosome translocations 7DL.7Ag and 1BL. 1RS in spring wheat. Crop Sci. 38:27-33.
Starzycki, S. 1976. Diseases, pests and physiology of rye. p. 27-61. In W. Bushuk (ed.) Rye: Production, chemistry and technology. Am. Assoc. of Cereal Chemists, St. Paul, MN.
Steel, R.G.D., J.H. Torrie, and D.A. Dickey. 1997. Principles and procedures of statistics. 3rd ed. McGraw-Hill, New York.
Villareal, R.L., O. Bafiuelos, A. Mujeeb-Kazi, and S. Rajaram. 1998. Agronomic performance of chromosome 1B and T1BL.1RS nearisolines in spring bread wheat Seri M82. Euphytica 103:195-202.
Villareal, R.L., E. del Toro, A. Mujeeb-Kazi, and S. Rajaram. 1995. The 1BL/1RS chromosome translocation effect on yield characteristics in a Triticum aestivum L. cross. Plant Breed. 144:497-500.
Villareal, R.L., E. del Toro, S. Rajaram, and A. Mujeeb-Kazi. 1996. The effect of chromosome 1AL/1RS translocation on agronomic performance of 85 [F.sub.2]-derived [F.sub.6] lines from three Triticum aestivum L. crosses. Euphytica 89:363-369.
Villareal, R.L., A. Mujeeb-Kazi, S. Rajaram, and E. del Toro. 1994. Associated effects of chromosome 1B/1R translocation in agronomic traits in hexaploid wheat. Breed. Sci. 44:7-11.
Villareal, R.L., S. Rajaram, A. Mujeeb-Kazi, and E. del Toro. 1991. The effect of chromosome 1B/1R translocation on the yield potential of certain spring wheat (Triticum aestivum L). Plant Breed. 106:77-81.
Abbreviations: HI, harvest index; STI, stress tolerance index; WUE, water-use efficiency.
|Printer friendly Cite/link Email Feedback|
|Author:||Ehdaie, B.; Whitkus, R.W.; Waines, J.G.|
|Date:||Mar 1, 2003|
|Previous Article:||Evaluation of spring cereal grains and wild triticum germplasm for resistance to Rhizoctonia solani AG-8. (Plant Genetic Resources).|
|Next Article:||Comparing a preliminary racial classification with a numerical classification of the maize landraces of Uruguay. (Plant Genetic Resources).|