| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
a Dep. of Agronomy and Plant Genetics, 411 Borlaug Hall, St. Paul, MN 55108
b USDA-ARS Plant Science Res. Unit and Dep. of Soil, Water, and Climate, 439 Borlaug Hall, St. Paul, MN 55108
c Dep. of Soil, Water, and Climate, 439 Borlaug Hall, Univ. of Minnesota, 1991 Upper Buford Circle, St. Paul, MN 55108
* Corresponding author (sheaf001{at}tc.umn.edu).
 |
ABSTRACT |
|---|
 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
Abbreviations: DAP, days after planting • PCR, polymerase chain reaction • PNL, Perennial Native Legume • %Ndfa, percentage of N derived from the atmosphere
|
INTRODUCTION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
Illinois bundleflower is compatible in mixtures with a diversity of warm-season grasses. In east-central Texas, established kleingrass (Panicum coloratum L.) stands interseeded with ‘Sabine’ Illinois bundleflower had greater forage yields than kleingrass monocultures in the second, third, and fourth years after seeding (Dovel et al., 1990). Mixtures of Illinois bundleflower accession PI 434011 with switchgrass (Panicum virgatum L.), sideoats grama (Bouteloua curtipendula Michx.), or indiangrass [Sorghastrum nutans (L.) Nash] in northeastern Kansas had higher forage yield and crude protein concentration than grass monocultures in the fourth and fifth years after establishment (Posler et al., 1993). Springer et al. (2001) showed that Sabine Illinois bundleflower was highly compatible in mixture with indiangrass.
Although Illinois bundleflower is known to contribute N in forage systems (Dovel et al., 1990; Posler et al., 1993; Springer et al., 2001), there is a paucity of information on its N2 fixation capability. Nodulation has been observed in 90% of the Mimosoideae (de Faria et al., 1989) including Illinois bundleflower (Allen and Allen, 1981). Kulakow et al. (1990) found that mean acetylene reduction rates of 70-d-old seedlings of Illinois bundleflower were comparable with those of soybean [Glycine max (L.) Merr.] and alfalfa (Medicago sativa L.), but also noted that rates varied significantly among accessions. However, the instantaneous rates of N2 fixation measured by the acetylene reduction technique cannot be extrapolated to obtain an accurate estimate of total N2 fixed across a growing season.
Integrated estimates of N2 fixation can be made by comparing N accumulation with non-N2–fixing plants (the total N difference technique) or by isotopic N methodologies. The latter depends on a 15N-labeled soil N pool, which is manifested in higher 15N concentrations in non-N2–fixing reference plants dependent on soil N than in N2–fixing plants, which incorporate both soil and unlabeled atmospheric N. In the 15N enrichment or isotope dilution technique, the soil N pool is labeled with an 15N-enriched source, whereas the 15N natural abundance method relies on the small but measurable elevation of 15N already present in most soils relative to the atmosphere (Chalk, 1985; Shearer and Kohl, 1986). In this study, we compared both isotope methods and the total N difference method as estimates of N2 fixation in monocultures of Illinois bundleflower. Our objective was to determine the in-field N2–fixation of three accessions of Illinois bundleflower managed as a forage crop in pure stands during the first 2 yr after seeding.
|
MATERIALS AND METHODS |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
15N natural abundance of total N in the top 15 cm of the soil at Becker, Rosemount, and Lamberton, as determined by a Europa Scientific Hydra 20/20 mass spectrometer (PDZ Europa, Cheshire, UK)1, was 7.47 ± 0.12, 7.85 ± 0.03, and 7.95 ± 0.16
(means ± standard error for six replicates), respectively.
|
|
Wild senna [Senna hebecarpa (Fernald) H.S. Irwin & Barneby], a warm-season perennial legume native to the northeastern and east-central USA (Irwin and Barneby, 1982), was grown as the non-N2–fixing reference plant for use in the comparisons involving 15N. Like many Caesalpinioid legumes, it is not nodulated (Allen and Allen, 1981), but in Minnesota, it generally exhibits similar emergence times and biomass accumulation patterns as Illinois bundleflower (E. Ristau, 1999, personal communication). Detailed descriptions of the root morphology of D. illinoensis and S. hebecarpa are lacking.
Field Experiment
The experiment was designed as a split plot at each of three locations with whole plots arranged in randomized complete blocks. There were six replicates per location. The whole-plot treatments were natural abundance and enriched levels of 15N. The split-plot treatments were the three Illinois bundleflower accessions and wild senna. Each plot measured 6 by 3 m. A 1.5-m-wide alley was maintained around each whole plot to reduce contamination of 15N natural abundance plots with enriched 15N.
Seed of the three populations of Illinois bundleflower were from DeHaan et al. (2003). The seed was mechanically scarified with sandpaper and inoculated with 5 g kg–1 of a commercial, peat-based inoculant for Desmanthus using 22 mL kg–1 seed of a 10% (w/v) sucrose solution as an adhesive. The inoculant contained two strains: Nitragin 43A1 and 43C2 (Liphatec, Milwaukee, WI). In 2000, seed was drilled in rows 15 cm apart on 25 May at Becker, 3 June at Lamberton, and 7 June at Rosemount. Seeding rates were 200 live seeds m–2 for Illinois bundleflower and 510 live seeds m–2 for wild senna. The higher rate for senna was based on previous data showing lower persistence and a less-open growth form than bundleflower (E. Ristau, 1999, personal communication). Average stand densities of Illinois bundleflower in 2000 were 157, 93, and 72 plants m–2 at Becker, Rosemount, and Lamberton, respectively. The corresponding densities of wild senna were 256, 171, and 155 plants m–2.
In the seeding year, 52 mL a.i. ha–1 of imazapic {Plateau, ±2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-methyl-3-pyridinecarboxylic acid, American Cyanamid Co., Parsippany, NJ} was applied before seedling emergence to control weeds in the Illinois bundleflower plots. In the second year, 68 mL a.i. ha–1 imazapic and 0.65 L a.i. ha–1 pendimethalin [Prowl, N-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine, American Cyanamid Co.] with 1.2 L ha–1 of an N-surfactant blend (Class Prefer-28, Cenex-Land O'Lakes Agronomy Co., Winona, MN) were applied before seedling emergence in the Illinois bundleflower plots. Pendimethalin inhibited growth of any seedlings from shattered first-year seed, ensuring purely 2-yr-old stands. Because wild senna does not tolerate imazapic (E. Ristau, 1999, personal communication), 0.5 L a.i. ha–1 of trifluralin (Treflan, 
,,-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine, Dow AgroSciences, Indianapolis, IN) was incorporated into the soil before planting the wild senna plots. In both years, hand weeding was also performed.
At 20 to 23 days after planting (DAP), a 0.2% (w/v) aqueous solution of 98 atom% 15N (NH4)2SO4 was applied to a 1.8-m2 area in the enriched plots by injection every 7.5 cm between every row for a total application rate of 0.2 g 15N m–2. Dinitrogen fixation should not have been inhibited by this low rate of N addition (2 kg N ha–1). The injection cannulas had pores at depths of 7.5 cm and 15 cm. In the second year, the solution was applied to a separate 1.8-m2 area in the enriched plots within 28 d after new shoots were visible. In both years, central areas in each plot were chosen for treatment to minimize edge effects.
Plants were harvested at maximum aboveground biomass (approximately 10% seedpod fill). In 2000, this occurred on 9 September at Lamberton, 10 September at Becker, and 14 September at Rosemount. In 2001, harvest dates were 14 August at Rosemount, 20 August at Becker, and 25 to 26 August at Lamberton. Aboveground biomass from a 0.8-m2 area within the 15N-treated area in the enriched plots was clipped at ground level by hand. A 0.8-m2 area also was harvested from the 15N natural abundance plots in a similar manner. Standing first-year stems were mowed and removed from the plots by hand-raking in April and May 2001, before emergence of second-year plants.
Samples were oven-dried for 48 h at 60°C and ground to pass a 0.5-mm screen. Total N concentration was determined using a LECO CN-2000 analyzer (LECO Corporation, St. Joseph, MI). The University of California-Davis Stable Isotope Facility determined isotopic composition of shoots. Shoots with enriched levels of 15N were analyzed on a Europa Scientific Integra mass spectrometer (PDZ Europa, Cheshire, UK), whereas shoots with natural abundance levels of 15N were analyzed on a Europa Scientific Hydra 20/20 mass spectrometer. Illinois bundleflower leaf tissue was analyzed for S and Mo concentration using a LECO S-144DR S analyzer (LECO Corporation, St. Joseph, MI) and an Applied Research Laboratories 3560 inductively coupled plasma spectrometer (Thermo ARL, Ecublens, Switzerland), respectively.
Calculations
The yield-independent measure %Ndfa represents the percentage of plant N derived from the atmosphere through N2 fixation. With natural abundance levels of 15N,
 | [1] |
15N is the per mil () departure from the 15N concentration of the atmosphere (which is at a constant 0.3663 atom% 15N, thus 15Natmosphere = 0 by definition), o is the non-N2–fixing reference plant, t is the N2–fixing plant grown under field conditions in which both soil and atmospheric N are available, and a is the N2–fixing plant grown under conditions in which only atmospheric N is available (Shearer and Kohl, 1986). Discrimination against the heavier 15N isotope during chemical reactions such as N2 fixation and N metabolism can lead to 15N enrichment in certain tissues (nodules), and 15N depletion in others (shoots) (Boddey et al., 2000). The resulting isotope fractionation is accounted for by the value 15Na.
If 15No is sufficiently large relative to 15Na or the converse, 15Na can be disregarded (Shearer and Kohl, 1986). Thus, at enriched levels of 15N, Eq. [1] reduces to:
 | [2] |
 | [3] |
These measures of %Ndfa are multiplied by N yield (which is calculated as dry matter yield per unit area x N concentration in the tissue) of the N2–fixing plant to give the amount of N2 fixed per unit area, a yield-dependent measure. Both methods assume that the N2–fixing and reference plants absorb N from the same pool of soil N across time and that the N2–fixing and nonfixing crops absorb 15N-labeled N and the plant-available soil N in the same ratio. An additional estimate of fixed N2 can be calculated as the difference in N yield between the N2–fixing plant and the reference plant. This total N difference method assumes that the N2–fixing and non-N2–fixing crops absorb equal amounts of soil N (Rennie, 1984).
Nodule Occupancy and 15N Fractionation
Because isotopic fractionation in plant shoots can vary according to rhizobial strain and host cultivar (Ledgard, 1989), a separate 15N was determined for selected rhizobium from each location x accession combination. For this determination, 10 nodules sampled from each location x accession combination in August 2001 were surface sterilized in 3% (w/v) NaOCl, rinsed repeatedly, and crushed in yeast-mannitol broth (Somasegaran and Hoben, 1994). Nodule preparations were streaked on yeast mannitol agar plates. Plates were incubated for 3 d at 25°C, then rhizobium were reisolated and resubcultured to ensure purity (Somasegaran and Hoben, 1994). Rep-PCR (polymerase chain reaction) genomic fingerprinting of cultures was performed using the BOXA1 primer 5'-CTACGGCAAGGCGACGCTGACG-3' (Veraslovic et al., 1994; Schneider and de Bruijn, 1996) and the results subjected to cluster analysis using BioNumerics software (BioSystematica, Devon, UK) to produce an unweighted pair group method with arithmetic mean dendrogram with the Pearson correlation as the similarity coefficient.
Isolates were transferred to yeast mannitol broth cultures. Seeds of the three accessions of Illinois bundleflower were chemically scarified and sterilized by soaking in concentrated H2SO4 for 5 min and then were washed repeatedly with sterile water. Plants were grown in 15-cm pots previously soaked in 3% NaOCl and filled with silica sand that had been washed with concentrated HCl. Six seeds were planted and then thinned to two per pot. Plants were inoculated at planting with 10 mL of broth culture of either the inoculant strains alone or a mixture of the inoculant strains plus indigenous strains from Lamberton. Plants were watered daily with N-free nutrient solution through capped glass tubes (Somasegaran and Hoben, 1994) and grown at 24°C during the day and 18°C at night, with a daylength of 16 h. Shoots were harvested 72 DAP, dried for 48 h at 60°C, and analyzed for natural abundance of 15N as above. The values of 15Na from the plants inoculated with the inoculant strain only were used for Becker and Rosemount, and the values of 15Na from the plants inoculated with the mixture of inoculant and indigenous strains were used for Lamberton (Table 3).
|
= 0.05 (Oelhert, 2000). |
RESULTS AND DISCUSSION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
15Na for plants inoculated with a mixture of indigenous strains than with the inoculant strains. Thus, we would have overestimated N2 fixation at Lamberton if we had based estimates for %Ndfa on the fractionation value from plants infected only with the inoculant strains rather than with a mixture of the inoculant strains plus indigenous strains. It should be recognized that the inoculant-adjusted values for 15Na may not reflect the relative occupancy of nodules by different rhizobial strains in the field, which was not estimated in this study. There was no rhizobial strain x accession interaction (P > 0.05).
|
|
|
|
The difference in %Ndfa between the two 15N methods at Becker and Rosemount may be due to the small differences in 15N between Illinois bundleflower and wild senna (0.75 at Becker and 0.10 at Rosemount, vs. 2.33 at Lamberton, averaged across accessions). Numerous physical and biological processes other than symbiotic N2 fixation can fractionate 15N, and can obscure the 15N signature of fixed atmospheric N2 (Handley and Scrimgeour, 1997). The contribution of these fractionation processes becomes important at low levels of 15N enrichment, and leads to invalidation of the assumption that fixed N2 and soil-derived N necessarily have unique 15N signatures (Handley and Scrimgeour, 1997). Therefore, the estimates of %Ndfa by the 15N natural abundance method probably should be considered less reliable than those given by the 15N enrichment method in this study.
Estimates of N2 fixed were similar for the 15N natural abundance and total N difference methods at Becker and Rosemount (P > 0.05), but estimates for the methods differed at Lamberton (P < 0.001), where estimates for the total N difference method were higher (Fig. 2). The pattern was reversed when comparing the 15N enrichment method with the total N difference method: the estimates for the two methods were similar at Lamberton (P > 0.05), but differed at Becker (P < 0.001) and Rosemount (P < 0.05), where estimates for the total N difference method were lower than for the 15N enrichment method.
Because of the low levels of N2 fixation in the seeding year, Illinois bundleflower may benefit from supplemental N fertilization to improve establishment (Hojjati et al., 1978). Although Dovel et al. (1990) achieved good establishment of Illinois bundleflower in kleingrass without supplemental N, bundleflower grew very slowly in the establishment year. In Minnesota, the northern edge of its range, Illinois bundleflower may be more difficult to establish because significant growth in the first year does not occur until July (DeHaan et al., 2003). The use of supplemental N fertilizer sufficient to increase vigor and establishment, but not in amounts so that nodulation is suppressed (Streeter, 1988), may be advantageous at low-fertility sites like Becker.
Second Year
Accessions had similar herbage yield, aboveground N yield, and N2 fixed estimated by the total N difference or 15N methods, or %Ndfa (P > 0.05) (Table 5). The lack of accession effects suggests that the first-year effects could have been due in part to factors such as seedling vigor and establishment, or perhaps in speed of nodulation. Second-year differences among the accessions noted by DeHaan et al. (2003), who grew Illinois bundleflower in space-planted nurseries, may have been masked in our experiments when plants were grown in dense stands.
|
A legume control with known yield potential was not included in this research. We are limited, therefore, to comparing data from Illinois bundleflower with published data from other trials. Mean yields of established stands of alfalfa, red clover (Trifolium pratense L.), and birdsfoot trefoil (Lotus corniculatus L.) at Rosemount were 13.2, 10.5, and 7.4 Mg ha–1, respectively (Minnesota Agricultural Experiment Station, 2002), compared with only 3.0 Mg ha–1 for Illinois bundleflower in our trial. In the same report, alfalfa yielded 12.0 Mg ha–1 at Lamberton, about 50% more than Illinois bundle-flower in our experiment in 2002. Lower yield of Illinois bundleflower compared with these cool-season legumes is likely due to its shorter growing season, the undomesticated status of the accessions used, or to less-than-optimum N2 fixation. Aboveground N yield of Illinois bundleflower was lowest at Rosemount, where the accessions averaged only 48 kg ha–1, which was less than first-year N yield at that site. Nitrogen yields at Becker and Lamberton were about 100 and 400% greater, respectively, than at Rosemount. Nitrogen yield of wild senna was more consistent than Illinois bundleflower, with low accumulation (<40 kg N ha–1) at all locations. On the basis of yields reported in the Minnesota cultivar trials cited above, and assuming a mean herbage N concentration of 26 g N kg–1 dry mass, harvested herbage N of established alfalfa, red clover, and birdsfoot trefoil at Rosemount averaged 340, 270, and 190 kg N ha–1, respectively, and alfalfa contained 310 kg N ha–1 at Lamberton. Harvested N in Illinois bundleflower at the most productive site (Lamberton) was, therefore, about 40% lower than alfalfa and about equal to birdsfoot trefoil.
As in the first year, the two 15N methods differed in estimated %Ndfa (P < 0.01), with higher estimates of %Ndfa at enriched than at natural abundance levels of 15N. The location effect was significant (P < 0.001). Plants at the low-N Becker site were most dependent on fixed N2, with %Ndfa ranging from 63 to 83% averaged across accessions. At Rosemount, %Ndfa of PNL534 and PNL541 was zero according to the 15N natural abundance method, whereas the 15N enrichment method estimated %Ndfa of 28 and 17% for these accessions, respectively. At Lamberton, %Ndfa across accessions was estimated at only 40% by the 15N natural abundance method, but 67 to 79% by the 15N enrichment and total N difference methods, respectively. In contrast to our results, Brandon et al. (1998), using the 15N natural abundance method, measured %Ndfa in inoculated second-year stands of the related species Desmanthus virgatus (L.) Willd. of 78, 48, and 26%, in an infertile sandy soil, a moderately fertile black earth, and a highly fertile clay soil, respectively. This response corresponds more closely to what is generally expected; that is, that legume reliance on symbiotic N2 fixation declines with increasing N supply (Allos and Bartholomew, 1959). We conclude that factors other than soil N supply were important in our experiment.
The two 15N methods did not differ in estimating N2 fixed at Becker and Rosemount (P > 0.05). The 15N methods estimated N2 fixation of about 70 kg ha–1 across accessions at Becker and <10 kg ha–1 fixed at Rosemount. At Lamberton, estimates of N2 fixed were different for the two methods (P < 0.01), with an estimate only one-half as large with the 15N natural abundance method as with the 15N enrichment method.
Only 12 kg N ha–1 was fixed at Rosemount according to the total N difference method, vs. 67 kg ha–1 at Becker and 142 kg ha–1 at Lamberton. The total N difference method produced higher estimates of N2 fixed than did the 15N natural abundance method at Lamberton (P < 0.001), but the methods were similar at Becker (P > 0.05). In contrast, the total N difference method gave lower estimates of N2 fixation than the 15N enrichment method at Becker (P < 0.001), but higher at Lamberton (P < 0.001), with no difference at Rosemount (P > 0.05). Except for the results at Rosemount, these estimates of N2 fixation by Illinois bundleflower compare favorably to those of birdsfoot trefoil in the north-central USA, which generally have ranged from 50 to 205 kg N ha–1, with a median of 90 to 100 kg N ha–1 annually (Seguin et al., 2000). Under irrigated, high-yield conditions at Becker, others have estimated that established alfalfa fixed between 240 and 340 kg N ha–1, depending on the method used to estimate N2 fixation (Lamb et al., 1995).
Plants at Rosemount were visibly chlorotic in the second year. The relatively wet spring and dry summer in 2001 may have adversely affected N2 fixation at Rosemount. Brandon and Date (1998) found that growth of Desmanthus virgatus was limited by S and Mo in a relatively fertile soil, and recommended a critical leaf S concentration of 2.0 g kg–1. Sulfur concentrations in Illinois bundleflower leaves were much lower at Rosemount (1.8 g kg–1) than at Becker (4.8 g kg–1) or Lamberton (5.2 g kg–1). Molybdenum concentrations were also lower in leaves from Rosemount (0.25 mg kg–1) than in leaves from Becker (2.1 mg kg–1) or Lamberton (3.0 mg kg–1). These results are quite surprising, given the high levels of soil organic matter at Rosemount (Table 1). Sulfur and Mo fertilization research may help clarify whether these nutrients limit Illinois bundle-flower growth.
The inoculant rhizobial strains accounting for almost all nodules at Rosemount and Becker may have been less than optimal in symbiotic efficiency considered. Dinitrogen fixation was highest at Lamberton, the only site within the native range of Illinois bundleflower. Over one-half of the nodules sampled were occupied by noninoculant indigenous strains at this site. The relative effectiveness of the inoculant and indigenous strains has not been characterized and is a promising direction for further investigations into the N2–fixation capabilities of Illinois bundleflower.
Another factor that deserves investigation is the role of mycorrhizal fungi in enhancing uptake of nutrients and N2 fixation in Illinois bundleflower. After conducting these studies, we learned that Illinois bundleflower is a host of Gigaspora spp. mycorrhizae (C. Picone, 2002, personal communication). If mycorrhizal inoculum present at Lamberton, where Illinois bundleflower is native, was not available at the other locations where the plant is introduced, differences in 15N among locations might result. Infection by mycorrhizae generally leads to lower 15N than noninfected plants (Handley and Scrimgeour, 1997), and would thus lead to higher estimates for %Ndfa. We did not inoculate with mycorrhizae in the experiment designed to determine 15N fractionation (Table 3). Inoculation with appropriate mycorrhizae also may improve access to nutrients that otherwise may limit plant growth.
Overall, %Ndfa was lowest at Rosemount in both years. Little or no N2 was fixed at Becker and Rosemount the first year, whereas 30 to 43 kg ha–1 was fixed at Lamberton, depending on the measurement method. Dinitrogen fixation did not occur at Rosemount in the second year, whereas apparent N2 fixation was 60 to 79 kg ha–1 at Becker and 67 to 142 kg ha–1 at Lamberton, depending on the measurement method.
Large differences in herbage yield among locations, but similar yields among accessions, indicate that conditions at one or two of the sites were suboptimal for Illinois bundleflower forage production. We expected to find larger differences among accessions in herbage yield, N yield, and apparent N2 fixation. We confirmed that indigenous rhizobial strains reduced 15N in herbage, compared with the inoculant strains. This implies that nodule occupancy should be determined when the natural abundance 15N method is used at locations that may differ in rhizobial strain presence and/or competitiveness. On the basis of our analysis of nodule occupancy, we recommend that additional rhizobial strains be sought for use as inoculum for this potential forage crop.
|
ACKNOWLEDGMENTS |
|---|
|
NOTES |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
Received for publication November 22, 2002.
|
REFERENCES |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSNOTESRESULTS AND DISCUSSIONREFERENCES |
|---|
This article has been cited by other articles:
|
|
 |
|
  M. P. Russelle, J. F. S. Lamb, N. B. Turyk, B. H. Shaw, and B. Pearson Managing Nitrogen Contaminated Soils: Benefits of N2-Fixing Alfalfa Agron. J., May 11, 2007; 99(3): 738 - 746. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. A. Fischbach, P. R. Peterson, C. C. Sheaffer, N. J. Ehlke, J. Byun, and D. L. Wyse Illinois Bundleflower Forage Potential in the Upper Midwestern USA: I. Yield, Regrowth, and Persistence Agron. J., May 13, 2005; 97(3): 886 - 894. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. A. Fischbach, P. R. Peterson, N. J. Ehlke, D. L. Wyse, and C. C. Sheaffer Illinois Bundleflower Forage Potential in the Upper Midwestern USA: II. Forage Quality Agron. J., May 13, 2005; 97(3): 895 - 903. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| The SCI Journals | Agronomy Journal | Vadose Zone Journal | |||
| Journal of Plant Registrations | Soil Science Society of America Journal | ||||
| Journal of Natural Resources and Life Sciences Education |
Journal of Environmental Quality |
||||
