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a USDA-ARS Plant Science Research Unit and Dep. of Agronomy and Plant Genetics, Univ. of Minnesota, 411 Borlaug Hall, 1991 Upper Buford Circle, Saint Paul, MN 55108
b Dep. of Agronomy and Plant Genetics, Univ. of Minnesota, 411 Borlaug Hall, 1991 Upper Buford Circle, Saint Paul, MN 55108
c Dep. of Plant Pathology, Ohio State Univ., 2021 Coffey Road, Columbus, OH 43210-1086
d Dep. of Horticulture and Crop Sci., Ohio State Univ., 2021 Coffey Road, Columbus, OH 43210-1086
e Dep. of Agronomy, Univ. of Wisconsin-Madison, 1575 Linden Drive, Madison, WI 53706
f Raymond F. Baker Center for Plant Breeding, Dep. of Agronomy, Iowa State Univ., 1204 Agronomy Hall, Ames, IA 50010
* Corresponding author (joannlamb{at}umn.edu)
| ABSTRACT |
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Abbreviations: CAIC, Central Alfalfa Improvement Conference CP, crude protein IVTD, in vitro true digestibility NDF, neutral detergent fiber NDFD, neutral detergent fiber digestibility NIRS, near infrared reflectance spectroscopy
| INTRODUCTION |
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Starting in 1956, forage yield trial results from across the upper Midwest were published annually by the Central Alfalfa Improvement Conference (CAIC). Hill et al. (1988) used data reported by the CAIC and determined that average forage yield for improved alfalfa cultivars released between 1971 and 1988 was 9% greater than the yield of Vernal. This contrasted with a report by these same authors (Hill and Rosenberger, 1985), using a different set of data, that attributed a yearly yield increase to cultivars released between 1971 and 1981 to <1%. Other researchers reported a 3% gain in forage yield between the mid-1950s and the early 1970s (Hill and Kalton, 1976; Elliott et al., 1972). Holland and Bingham (1994) grew alfalfas from three eras: 1898 to 1910, 1940 to 1953, and 1979 to 1985 at one location in Wisconsin. They concluded that mean forage yields increased between each era with a greater rate of increase in yield occurring between the second and third era than between the first and second era. However, data reported in their research showed that forage yield from some individual cultivars from the second and third eras were similar.
In contrast to the aforementioned results, Wiersma et al. (1997) used CAIC yield data to report a slight but statistically significant decline in forage yield for cultivars released between 1978 and 1996. Volenec et al. (2002) used an updated version of the database created by Wiersma et al. (1997) to compare first harvest yields of alfalfas released between 1907 and 1998. They evaluated both the highest and average yield of landraces or cultivars released in each year and reported no improvement or a small decline in forage yield for more recently released cultivars. Conflicting reports on changes in forage yield of cultivars released during the past century cause speculation on the reality of yield improvement in alfalfa.
Yield improvement in forage crops during the past century has lagged far behind that of annual grain crops (Brummer, 1999). Some factors contributing to the slower rate of progress for alfalfa include the dynamics related to survival and overwintering of a perennial growth habit; multiple years of evaluation before selection decisions can be made; and inability to repartition plant assimilates to maximize harvest index, as has been done in annual grain crops, since the entire aboveground portion of the alfalfa plant is harvested (Hill et al., 1988). Another potential reason for reduced yield improvements in alfalfa has been the major focus of most U.S. alfalfa breeding programs on disease and pest resistance. Breeding efforts during the past five decades have resulted in nearly all currently marketed alfalfa cultivars having high levels of resistance to a wide variety of important diseases and insects (AOSCA, 2002). Consequently, resistant cultivars should have superior yields compared with susceptible cultivars when grown in environments that favor pest development. While breeding for pest resistance can play a role in realizing yield potential, it likely does not increase the frequency of genes for yield per se in populations under improvement.
A possible explanation for the previously mentioned conflicting reports on changes in yield for new alfalfa cultivars is that yield totals were compiled from trials conducted at numerous locations across several years ignoring germplasm by year (age of the stand) and germplasm x environment (location) interactions. Hill and Baylor (1983) reported that response patterns related to age of the stand and disease infestation would occur for total yield in a perennial forage like alfalfa, and that these age and disease resistance effects would not be reflected in the cultivar mean across all locations.
Increasing forage yield has once again become a focus for discussion among alfalfa researchers (Brummer, 1999; Volenec et al., 2002). In an attempt evaluate genetic improvement in alfalfa during the past 60 yr, while accounting for genotype x environment and age interactions, our objective was to compare the forage yield, and assess persistence and nutritive value of alfalfa cultivars released from 1940 to 1995, side by side in replicated trials for 5 yr at four upper Midwest locations.
| MATERIALS AND METHODS |
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All plots were mown in July of 1999 and subsequent forage yields were estimated from a 0.9- by 5.2-m swath cut through each plot at a stubble height of 5 to 7.5 cm. At all locations, the target maturity for harvest was bud to early flower, with the last harvest in each growing season taken in early to mid-September. The numbers of harvests taken annually to evaluate forage yield differed at the four locations. At Iowa, two, three (third harvest in 2000 not recorded because of harvest error), four, four, and four harvests were taken in 1999, 2000, 2001, 2002, and 2003 respectively, for a total of 17 harvests. At Minnesota, one harvest was taken in 1999, three harvests each in 2000 to 2002, and four in 2003, for a total of 14 harvests. One harvest was taken in the establishment year, and four harvests were taken each in 2000 to 2003, for a total of 17 harvests at Ohio. Two harvests were taken in 1999, and four harvests each year for 2000 to 2002, for a total of 14 harvests at Wisconsin. Hand grab samples (minimum 300 g wet weight) were taken from harvested materials in at least 10% of the plots at each harvest, dried at 55°C, reweighed and used to calculate dry matter yields. All yields were recorded on a dry matter basis. Final stand densities of all plots were estimated as percentage ground cover m2 (at Iowa, Minnesota, and Ohio in October 2003) or number of stems m2 (at Wisconsin in October 2002).
Nutritive Value Comparisons
Subsamples were taken from the first and third harvests in 2000 and 2001 at Minnesota, Ohio, and Wisconsin to assess any changes in nutritive value among these cultivars released during the past five decades. Plots were hand clipped to a stubble height of 5 cm, in a minimum of three random, nonborder 1-ft2 areas to produce a minimum sample size of 300 g wet weight. These subsamples were dried at 55°C in forced-air ovens, weighed, and ground through a 1-mm screen in preparation for nutritive value analysis.
Crude protein (CP), neutral detergent fiber (NDF), and in vitro true digestibility (IVTD) were determined via near infrared reflectance spectroscopy (NIRS) analysis (model 6500, NIRSystems, Silver Springs, MD)1 using NIRS equations developed for alfalfa in Minnesota. Equations for NIRS were developed using the software program Calibrate (NIRS 3 version 4.0, Infrasoft International, Port Matilda, PA) with modified partial least squares regression option (Shenk and Westerhaus, 1991a, 1991b). Random subsets of 10 samples were chosen and subjected to conventional chemical analysis for CP (Kjeldahl N x 6.25), NDF, and IVTD (Goering and Van Soest, 1970); and used as monitoring sets. Predicted values for CP, NDF, and IVTD were adjusted for bias based on conventional analysis results from the monitoring sets. Neutral detergent fiber digestibility (NDFD) for each sample was calculated from NDF and IVTD using equations developed by Hoffman et al. (2001).
Statistical Analyses
Analysis of variance was conducted to estimate the effects of year, location, and cultivar or cultivar-release date on forage yield and quality (PROC GLM; SAS Institute, 2001). Locations were considered random and years and cultivars were fixed. Means and standard errors were calculated for forage yield for each cultivar-release date. When cultivars differed for forage yield or final stand score, regression analyses were conducted to describe the response in relation to their release dates (P
0.01) (PROC REG; SAS Institute, 2001). Means and LSD (0.05) were calculated for nutritive value traits for each cultivar.
| RESULTS AND DISCUSSION |
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Years, locations, and cultivar-release date and all two- and three-way interactions among these main effects impacted forage yield (Table 2). The year x location x cultivar-release date interaction demonstrated that forage yields among the cultivars differed in each year within each location. Therefore, the ANOVA for forage yield among the cultivar-release dates was conducted separately for each year within each location (Table 3). Regression analyses of forage yield vs. cultivar-release date were conducted for those years within each location where the cultivars differed.
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In the first production year (2000) at Minnesota, cultivars differed in forage yield (Table 3). Regression analysis demonstrated that the relationship between forage yield and cultivar-release date was minimal (Fig. 1C). Vernal (1953) and 525 (1962) yielded less than the other cultivars in the first production year. The older cultivars released in the 1940s yielded the same as cultivars released during the latter three decades. A slight increase in forage yield for more recently released cultivars occurred again in the second production year (2001). In 2001, 520 (1969) had the highest yield, while Atlantic (1940), 525 (1962), and Vernal (1953) were lower in forage yield compared with the rest of the cultivars. In 2002, no differences in forage yield among the cultivars occurred. Difference in forage yield was found among the cultivars in 2003, but no relationship with release date was demonstrated. In the final 2 yr of the experiment, cultivar-release date appeared to have little influence on forage yield at Minnesota.
At Ames, no differences in forage yield among cultivars released between 1940 through 1995 were shown (Table 3 and Fig. 1D). The oldest cultivars, Atlantic (1940) and Ranger (1942), had comparable forage yields to the rest of the cultivars, including Jade II (1995), in every year of the experiment.
Final Plant Stand Density
Final stand density estimates of the cultivars were different at each of the four locations (Fig. 2
). As with forage yield, final stand density was similar (average = 90%) for all cultivars at Iowa. Stand survival among the cultivars was different at the three remaining locations. At Minnesota, final stand density ranged from 73 to 95% ground cover with Atlantic (1940), Saranac (1965), 525 (1962), Blazer (1978), and 520 (1969) having the greatest stand loss. Ranger (1942), Vernal (1953), Cayuga (1961), and Magnum III (1988) were intermediate, while 526 (1981) and all cultivars released between 1990 and 1995 had the greatest stand survival. The range in final stand densities among the cultivars at Ohio was much wider (3381%) compared with Minnesota. Saranac (1965), Atlantic (1940), and Ranger (1942) had the most profound plant stand losses. The remaining cultivars released between 1953 and 1981 were intermediate in plant stand, and all cultivars released in 1988 or later had the greatest plant stand density. At Wisconsin, final stand estimates ranged from 277 to 519 stems m2. DK 127 (1994), Wintergreen (1994), Garst 645 (1990), WL 324 (1994), and Magnum III (1988) had the highest stem counts, while Saranac (1965), 525 (1962), Ranger (1942), and Atlantic (1940) had the lowest stem counts.
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The conflicting yield responses across locations and years imply that factors other than yield per se influenced our results. Simple correlations between total yield per plot and final stand density per plot were greater at Wisconsin (r = 0.73, P
0.001) and Ohio (r = 0.65, P
0.001) compared with Minnesota (r = 0.48, P
0.001) and Iowa (not significant). The disparity in the relationship between yield and final stand density were likely influenced by biotic and environmental stresses unique to each location including differences in soil type, temperature, and moisture regimes proscribed by climate and incidence of disease or pests. At Ohio, the plots were evaluated annually for incidence of disease. At Ohio, Ariss (2005) found significant negative relationships between the total number of diseased stems [primarily Fusarium wilt, Fusarium oxysporum Schlecht f. sp. medicaginis (Weimer) Snyd. and Hans., and anthracnose, Colletotrichum trifolii Bain and Essary] per plot and total yield (r = 0.65, P
0.01), final stand density (r = 0.71, P
0.01), and release date (r = 0.65, P
0.01). Results at Ohio indicated that recently released cultivars (19881995) had fewer diseased stems, denser final stands, and higher forage yield compared with older cultivars.
Multiple disease resistance in marketed alfalfa has increased with time as newer cultivars were released (Table 1). Cultivars rated as the most susceptible to disease (Atlantic, Ranger, and Saranac) had the greatest stand losses and the lowest yields at Ohio. We speculated that the increased disease resistance advantage of recently released cultivars improved stand survival and protected yield potential at Ohio. Disease infestation assessments were not conducted at the other three locations. However, at Wisconsin, results were similar to those found at Ohio; cultivars with higher levels of multiple pest resistance (released between 1988 and 1995) had higher yields and greater final stem counts compared with the rest of the cultivars. By fall 2002, stand scores (stems m2) of the more susceptible cultivars were so low that the decision was made to terminate the study at Wisconsin. At Iowa and Minnesota, where differences in plant stand did not occur or were minimal, forage yields were similar for all cultivars regardless of release date. We concluded that evidence for changes in forage yield for cultivars released between 1940 and 1995 was environmentally dependent. In environments where conditions lead to plant stand losses, recently released cultivars with multiple disease resistance had a yield advantage over older cultivars, but in environments where no differences in plant density occurred, older cultivars yielded the same as the improved cultivars.
| ACKNOWLEDGMENTS |
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| NOTES |
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| REFERENCES |
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