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a Dep. of Plant Sci., Macdonald Campus of McGill Univ., 21,111 Lakeshore Rd., Ste. Anne de Bellevue, QC, H9X 3V9, Canada
b Inst. de Malherbologie, P.O. Box 222. Ste. Anne de Bellevue, QC, Canada
afm{at}nrs.mcgill.ca
| ABSTRACT |
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| INTRODUCTION |
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from the soil during crop production has adverse effects on soil properties and is an economic loss. Ground and surface water contamination can be caused by plant nutrients applied in excess of crop uptake. Nitrogen management goals are to promote N uptake and maximize crop yield while minimizing N losses. Losses of mineral N are a result of immobilization, volatilization of NH3, leaching, and denitrification (Bock, 1984). These last two processes are of concern as potential sources of contaminants of ground and surface waters and of the atmosphere. Sweet corn in eastern Canada may be a problem crop due to high N fertilizer rates.
Growing cover crops after sweet corn harvest may minimize residual soil NO-3N level and reduce NO-3N content of gravitational water (Karlen and Doran, 1991; Miller et al., 1992; Brandi-Dohrn et al., 1997). Legumes are difficult to study as they are both a sink and a source of N. Nitrogen supplied by hairy vetch (Vicia villosa Roth) and crimson clover (Trifolium incarnatum L.) in cover crop experiments ranged from 72 to 149 kg N ha-1 (Ebelhar et al., 1984; Hargrove, 1986; Holderbaum et al., 1990; Clark et al., 1995; McVay et al., 1989). Nonlegume cover crops have been associated with reducing N leaching loss, but the equivalent fertilizer N retained against leaching is estimated with difficulty. Studies of legume vs. nonlegume cover crops are needed in order to compare their capacity to decrease soil NO-3N and release N to the subsequent crop.
The denitrification process in agricultural soils is affected by NH+4N and NO-3N concentrations (De Klein and van Logtestijn, 1994), water content (Davidson, 1992), available C content (Rolston, 1981), and temperature (Mancino et al., 1988). Incorporation of available C from cover crops can increase denitrification rates (Aulakh et al., 1983). Production of crops such as sweet corn, which have high N rates and early maturity, might benefit from the use of cover crops to absorb excess fertilizer N in the late summer and fall growth. The objectives of the study were to quantify the effect of N fertilizers and cover crop species on subsequent sweet corn yield, N uptake, potential nutrient losses in gravitational water, and denitrification.
| Materials and methods |
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Two liters per hectare of Basagran [480 g L-1 bentazon; 3-(1-methylethyl)-(1H)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide] was applied on 22 June 1994, to control nut sedge (Cyperus rotundus L.) on the Ste. Rosalie site. In April 1995 and June 1996, the Ste. Rosalie plots were sprayed with 5 L ha-1 Roundup [356 g L-1 glyphosate, N-(phosphonomethyl)glycine] directed between the rows, 2.8 L ha-1 Hoe-grass 284 {284 g L-1 diclofop-methyl; methyl ester of (±)-2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid}, 1 L ha-1 Pardner (280 g L-1 bromoxynil; 3,5-dibromo-4-hydroxybenzonitrile), and 2.25 L ha-1 Basagran Fort (480 g L-1 bentazon). Herbicides were applied post emergence. No herbicides were used in the St. Bernard site. Corn was harvested by hand on 5 Aug. 1994, 24 July 1995, and 20 July 1996; 25 ears were randomly harvested from the central two rows and a five-plant subsample was taken from each plot to assess yield components. Samples were dried at 70°C and ground to pass a 1-mm sieve (18 mesh) prior to analyses.
Experimental areas were cultivated with a tractor-mounted rototiller before seeding cover crops. Six cover crops and a control treatment (no cover crop) were used. Cover crops were seeded on 8 and 10 Sept. 1994 and 5 and 6 Sept. 1995, using a 5-row, 76-cm small-plot forage seeder. Cover crop seeding rates were 12 kg ha-1 for red clover, 22 kg ha-1 for crimson clover, 10 kg ha-1 in 1994 and 20 kg ha-1 in 1995 for forage radish, 10 kg ha-1 for canola, 142 kg ha-1 for barley, and 35 kg ha-1 for annual ryegrass. Forage radish seeding rate was increased to 20 kg ha-1 in 1995, due to low plant populations in 1994.
Harvesting of cover crop biomass was completed on 28 October in 1994 and on 25 October in 1995, using a 53.4- by 53.4-cm quadrat. Due to unusual conditions, the cover crop continued to grow in 1994 after sampling. Ten plants were dug from each plot to estimate root and shoot biomass and NPK concentrations. Plant roots were removed with help of a small shovel, and washed carefully to remove the soil. All plant samples were dried at 70°C and weighed. Plots were plowed after sampling. Treatments were repeated in time in the same plots throughout the study.
Soil NO3 and gravitational water measurements were carried out only on high N rate plots, on forage radish, red clover, ryegrass, and control plots. Samples for NO3N were obtained before sweet corn seeding in spring and in late fall when cover crop growth ceased. Samples at the Ste. Rosalie site were taken to a depth of 100 cm in 20-cm increments; samples at the St. Bernard site were taken to a depth of 60 cm in 20-cm increments.
Zero-tension lysimeters were installed to collect gravitational water in November and removed in early May. Sampling cylinders (6.0 cm i.d. by 90 cm) with one closed end and three holes (0.3 cm diam.) were installed in the selected treatment plots, with three replicates, after sweet corn harvest for both sites in 1994 and 1995. Cylinders were pushed into the soil to 55 cm below the soil surface after removing soil with hydraulically inserted sampling tubes of the same diameter. The open end of the cylinder was covered with a glass jar to prevent precipitation entry and evaporation. Soil water at zero tension could enter but not leave the cylinder. Soil solution samples were collected periodically whenever water was found from the cylinder with a rubber hose connected to a 60-mL syringe. Both rubber hose and syringe were washed with distilled water after each sample and rinsed with the next sample to minimize contamination. At each sampling, approximately 70 mL of soil solution was collected from each cylinder for determination of NO-3N, NH+4N, P, and K on 28 Mar. 1995, 22 Jan. 1996, 2 May 1996, and 8 May 1996.
Denitrification measurements were made during the corn growing season using the technique of Aulakh et al. (1983). Soil cores (2.5 cm i.d. by 15 cm) were collected from the 0- to 15-cm depth from forage radish, red clover, ryegrass, and control plots and were incubated in 2-L bottles at ambient temperatures. The concentration of N2O was determined on gas samples from incubated soil by gas chromatography.
Soil samples were extracted using the Mehlich 3 procedure (Tran and Simard, 1993); P and K were determined with an automated analyzer. Organic matter analyses used the WalkleyBlack procedure (Nelson and Sommers, 1982). Soil particle size distribution was measured by hydrometer (McKeague, 1976, p. 1626).
The mineral N lost from the profile during the fall and winter of 19941995 and 19951996 was calculated using changes in soil NO3 and estimated leaching losses from gravitational water assuming leaching losses of 215 to 236 mm of excess water (Zhang and MacKenzie, 1997). Ammonium and NO-3N were extracted from approximately 10 to 15 g of soil from each depth by shaking in 100 mL of 1 M KCl for 1 h. Suspensions were filtered and filtrates analyzed colorimetrically (Keeney and Nelson, 1982). Plant total N, P, and K were determined by digesting 0.250 g of oven-dry plant tissue using H2SO4 and H2O2 and determining N and P colorimetrically and K by flame photometry (Thomas et al., 1967).
Statistical analyses were conducted using Analysis of Variance (ANOVA) and General Linear Model (GLM) procedures of Windows SAS Version 6.11 (SAS Institute, Cary, NC). Comparisons among treatments were made using orthogonal contrasts. Polynomial trend comparisons were used to examine N treatment effects.
| Results |
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Cover Crop Dry Matter Production
Cover crop root and shoot yields varied with species, except for the Ste. Rosalie shoot biomass in 1994 (Table 3)
. Shoot biomass at the St. Bernard site in 1994 was highest from barley and ryegrass, followed by forage radish, canola, and red and crimson clover. Estimated root biomass in 1994 was highest for ryegrass at both sites. In 1995, shoot biomass ranged from 255 to 3120 kg ha-1. Cover crop species effects were similar across both sites. Forage radish produced the highest shoot and root biomass; red clover produced the lowest aboveground biomass.
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Cover Crop N Uptake
Cover crop N uptake paralleled dry matter production at both sites for both years. There was no effect of N fertilizer in either year at either site (Table 4)
. Root and shoot N uptake was affected by cover crop species excepted for shoot N in 1994 at the Ste. Rosalie site. At the St. Bernard site, shoot N uptake was higher with barley, ryegrass, forage radish, and canola and lower with crimson and red clover. In 1995, forage radish had the highest total shoot and root N at both sites, followed by canola at the Ste. Rosalie site, and canola and barley shoot values at the St. Bernard site.
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Denitrification Values
Denitrification was not influenced by cover crops at either site, at any sampling date (data not shown). Seasonal variations were noted, and values ranged from lows in October of 0 to 21 g ha-1 N d-1 to highs in June of 8 to 95 g ha-1 N d-1.
| Discussion |
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Both methods for estimating NO-3N leaching losses showed similar overall trends between soils. Estimated losses of NO-3N were higher at the St. Bernard site than Ste. Rosalie site using either method. This could be due to reduced movement of NO-3N over the winter due to a higher clay content in Ste. Rosalie soil than in St. Bernard soil, or due to rapid surface water movement down fissures in the high-clay Ste. Rosalie soil, reducing N levels in the leaching water.
Differences in estimates of NO-3N loss between methods varied with the year. In the winter of 19941995, at the Ste. Rosalie site, losses of NO-3N calculated by each method were similar for control plots, but at St. Bernard, soil losses estimated using the soil gravitational solution method were higher than when using the sequential soil core sample method. In both soils, losses during winter 19951996 calculated from soil solution were less than those obtained from the sequential soil core sample method. This difference could be due to rapid surface preferential flow of water through soil macropores or fissures diluting gravitational soil solution NO-3N levels (Francis et al., 1994). Amount and distribution of over-winter precipitation was similar for both years, at 396 and 386 mm (November to March, inclusive), and was probably not a major cause of difference between years. Francis et al. (1994) stated that the sequential soil core sample method could overestimate losses if denitrification was significant during the fall to spring period. However, our denitrification rates were low in this period. Thus, denitrification is not considered to have been a significant component of the N cycle in the fall to spring time of the year.
In 1994, species differences were not pronounced, due to low dry matter production. In 1995, when the cover crop dry matter yields were higher, species effects were large. Barley, forage radish, and canola generally produced the highest shoot and root dry matter at both sites.
Root uptake N tended to parallel shoot N uptake but was only 10 to 20% of the total N uptake. Our results support previous observations of percentage of N contained in the cover crop shoots. Jensen et al. (1944) and Mitchell and Teel (1977) reported that more than 80% of the N in several forage species was contained in the shoots. Touchton et al. (1982) concluded that no more than 30% of N can be expected in the root system.
Losses of NH+4N, P, and K were not affected by cover crop, due to their low mobility in soils or retention on cation exchange complexes. With adequate cation exchange capacity in these soils, cations such as NH+4N and K+ would remain largely adsorbed. Phosphorus was largely immobile, due to fixation in the soils.
The highest denitrification values occurred during growth of the sweet corn, because residual N levels in the soil were high (De Klein and van Logtestijin, 1994) and temperature was high (Mancino et al., 1988) compared with the period of cover crop growth, when the temperature was low. The hypothesis that denitrification would be increased with cover crop (Aulakh et al., 1983) use was not supported, and cover crops following sweet corn had no apparent effect on denitrification.
Criteria for cover crop selection should include ease of establishment, effective absorption of excess fertilizer N, reduction of nutrient loss by leaching, and subsequent release of N for growth of a following crop. Under these criteria, establishment was most successful with forage radish, barley, and canola. In contrast, legumes and ryegrass resulted in disappointing stands and their effectiveness was limited under the short-term period of growth used in the experiment. Cover crops achieved the objectives of reducing potential fall leaching and ensuring adequate soil N levels the following spring.Jensen Frith 1944
| NOTES |
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Received for publication June 11, 1998.
| REFERENCES |
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