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Published online 17 June 2005
Published in Agron J 97:1037-1045 (2005)
DOI: 10.2134/agronj2003.0212
© 2005 American Society of Agronomy
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Nitrogen Management

Fate of Nitrogen-15 in a Long-Term Nitrogen Rate Study

I. Interactions with Soil Nitrogen

W. B. Stevensa,*, R. G. Hoeftb and R. L. Mulvaneyc

a Northern Plains Agric. Res. Lab., 1500 N. Central Ave., Sidney, MT 59270
b Dep. of Crop Sci., 1102 S. Goodwin Ave., Univ. of Illinois, Urbana, IL 61801
c Dep. of Nat. Resour. and Environ. Sci., 1102 S. Goodwin Ave., Univ. of Illinois, Urbana, IL 61801

* Corresponding author (bstevens{at}sidney.ars.usda.gov)

Received for publication September 2, 2003.

    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 
A better understanding of how N management practices affect transformations and movement of fertilizer N may lead to more efficient N management. The objectives of this work were to determine how long-term N fertilizer history in a continuous corn (Zea mays L.) production system affects (i) movement of fertilizer N through the soil profile and (ii) cycling of fertilizer N between available and nonavailable soil forms. Nitrogen-15-labeled ammonium nitrate (15NH415NO3) was applied at 0, 67, 134, 201, or 268 kg N ha–1 to subplots of long-term N rate plots. Twenty to 55% of labeled N was converted into either organic or clay-fixed forms during the first growing season, with the percentage decreasing with increasing N application rate. Significantly more N was released from nonavailable forms in plots where the historical N application rate had exceeded the long-term optimum (186 kg ha–1) than in plots that received lower rates. Little fertilizer-derived N leached from the profile during the first growing season, but losses did occur during the off-season and subsequent growing season when N application rate was higher than the optimum. It was concluded that a history of excessive N application may decrease response of subsequent crops to fertilizer N due to greater release from nonavailable N forms, most likely as a result of increased mineralization of crop residues and recently formed soil organic N.

Abbreviations: KMI, Kjeldahl nitrogen minus inorganic (nitrogen) • TKN, total Kjeldahl nitrogen


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 
APPLICATION OF SYNTHETIC N fertilizer is a convenient, economical, and effective way to meet the N demands of modern high-yielding crops such as hybrid corn. Yet despite obvious benefits, there is evidence that N fertilizer use leads to increased levels of NO3 in surface and ground water resources (Spalding and Exner, 1993; Randall and Mulla, 2001). Because the risk of NO3–N loss is greater with excessive N application rates than with rates near the agronomic optimum (Jolley and Pierre, 1977), careful N management can significantly reduce the environmental risks of N fertilizer use by reducing postharvest NO3 levels (Karlen et al., 1996). However, N application rates are difficult to optimize, owing to the uncertainty inherent in predicting net mineralization of soil organic N, which may vary greatly according to management and climatic variables.

Traditional N recommendation approaches, which typically include credits for previous legume crops, manure, and/or residual soil NO3, have been only moderately successful at predicting N fertilizer requirements. In an Illinois study, Brown et al. (1993) compared three methods of calculating N fertilizer requirements for corn—the proven yield method described in the Illinois Agronomy Handbook (Hoeft, 2000), the preplant nitrate test, and the presidedress nitrate test (PSNT) developed by Magdoff et al. (1984). All three approaches performed less than satisfactorily in many cases when compared with actual N response for 75 site-years. Of particular interest were 12 nonresponsive site-years where recommended N application rates greatly exceeded N requirements. Because residual NO3–N was not exceptionally high at these sites, the lack of response was attributed to unexpectedly high mineralization of organic N during the growing season.

Recent work by Mulvaney and Khan (2001) has identified serious defects in steam distillation methods of fractioning hydrolyzable soil N and has led to simple diffusion techniques that eliminate these defects. When the latter techniques were applied to some of the soil samples collected by Brown et al. (1993), a considerably higher concentration of amino sugar N was obtained for 11 nonresponsive sites than for seven responsive sites, whereas no consistent difference was observed in their concentrations of total hydrolyzable NH4–N or amino acid N (Mulvaney et al., 2001). Subsequent work has led to a simple soil test for estimating amino sugar N as a means to detect sites where corn does not respond to N fertilization (Khan et al., 2001).

While the work of Mulvaney et al. represents a significant stride toward understanding how N cycling affects response to fertilizer N, more information is needed regarding the effects of rate and time of N application and N source on the relative contributions of mineralized N and fertilizer N to plant N uptake. Numerous studies have been conducted to evaluate the effects of cropping sequence and tillage on N cycling, among the more recent being those by Kitchen et al. (1997), Karlen et al. (1998), Wienhold and Halvorson (1999), and Ottman and Pope (2000). Fewer studies have addressed the effects of previous fertilizer N application rate on N mineralization and subsequent crop response to N fertilization. Moreover, the findings are rather difficult to interpret as in some cases, a history of heavy N fertilization has promoted net mineralization (Shen et al., 1989; Motavalli et al., 1992; Kolberg et al., 1999) while in others, the opposite effect has been observed (Lovell and Hatch, 1998; Carpenter-Boggs et al., 2000).

The use of 15N-labeled fertilizer has obvious application in long-term studies to evaluate fertilizer effects on soil N availability. This approach has been employed in long-term N rate experiments with wheat (Triticum aestivum L.; Powlson et al., 1986) and barley (Hordeum vulgare L.; Glending et al., 1997) while 15N-tracer research with corn has been limited to plots with no documented history of long-term N application rate (Kitur et al., 1984; Sanchez and Blackmer, 1988; Reddy and Reddy, 1993). Our objectives were to investigate the effects of previous fertilizer N application rate on (i) the movement of fertilizer N through the soil profile and (ii) cycling of fertilizer N between available and nonavailable soil forms.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 
Location
The experiment was conducted on plots of a long-term N fertilizer rate study at the University of Illinois Northwest Research and Education Center located near Monmouth, IL. Urea had been applied annually to plots at rates of 0, 67, 134, 201, or 268 kg N ha–1, such that any given plot received the same application rate in every year since the establishment of the continuous corn study in 1983. Soil within the plot area is classified as a moderately permeable Muscatine silt loam (fine-silty, mixed, mesic Aquic Hapludolls) formed in a deep upland loess deposit on nearly level topography. The soil is classified as somewhat poorly drained, but no tile drainage exists within the plot area.

Treatment Application and Cultural Practices
Experimental units of the original long-term N rate study were 6.1 by 18.3 m in size and consisted of eight corn rows spaced 75 cm apart. To facilitate the establishment of microplots for 15N application without eliminating the main-plot harvest area, each experimental unit was divided into two 3.05- by 18.3-m areas, one of which was used for collection of grain yield data (main harvest area) and the other for establishment of 2.3- by 3.05-m 15N microplots. By the end of the 3-yr study, each experimental unit contained three microplots, a new microplot being established in each year (Fig. 1) . Urea was applied to the main-plot harvest area and immediately incorporated by tillage. Hybrid corn (DK 623, Dekalb Genetics Corp., DeKalb, IL) was then planted using a four-row tractor-drawn planter at a rate of 75500 seeds ha–1. Just after planting, 15NH415NO3 was applied to the microplot and unlabeled NH4NO3 to the remainder of the 3.05- by 18.3-m area that contained the microplots. To achieve a uniform application of labeled N, 2 L of 15NH415NO3 solution was applied to microplot areas using a CO2–pressurized spray boom, which spanned the entire width of the microplot. The boom was manually moved at a speed sufficient to travel the length of the plot 6 to 10 times before the solution was completely drained. A 3.1 atom% 15NH415NO3 solution was prepared for each experimental unit by dissolving an enriched stock reagent (10 atom% 15N, Icon Services, Summit, NJ) and unlabeled reagent grade NH4NO3 (0.3663 atom% 15N) in 2 L of distilled water in amounts that resulted in an N application rate equal to that of the main-plot area.



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Fig. 1. Location of 15N microplots and harvest area within main plots of the long-term N rate study at Monmouth, IL.

 
Weed control was accomplished with postemergence herbicide applications and interrow cultivation. In 1994, atrazine (3.5 kg a.i. ha–1) plus S-metolachlor (2.7 kg a.i. ha–1) was applied preplant, and bromoxynil octanoate (2.2 kg a.i. ha–1) plus primisulfuron-methyl (0.05 kg a.i. ha–1) was applied postemergence. In 1995 and 1996, alachlor (3.4 kg a.i. ha–1) was applied preplant, and dicamba (0.47 kg a.i. ha–1) plus atrazine (0.87 kg a.i. ha–1) was applied postemergence. The microplot areas were weeded by hand to prevent significant amounts of N from accumulating in weeds. Plant population was determined at the V4 growth stage, and microplot areas were thinned to a uniform population of 69500 plants ha–1.

Fall tillage consisted of one chisel plow operation after all harvest and sampling operations were completed. Care was taken during the tillage operation to prevent excessive movement of soil and crop residues within the plot area.

Sample Collection
Soil samples for determination of initial chemical and physical characteristics were collected in the spring before application of N fertilizer. Following application of labeled N, soil samples were collected from a 1.5- by 1.5-m area within the microplots in the fall soon after crop harvest. Microplots were also sampled in the spring and fall of the second and third growing seasons following 15N application until the termination of the study in the fall of 1996. Soil cores were extracted from a depth of 120 cm and divided into five depth increments (0 to 15, 15 to 30, 30 to 60, 60 to 90, and 90 to 120 cm). Three cores were extracted from each microplot at each sampling time using either a 1.9-cm-diam. hand probe or a Giddings hydraulic soil probe equipped with a 3.5-cm-diam. sampling tube. Samples were maintained at field moisture and frozen until analysis.

Sample Analysis
Initial levels of total C and total N were determined on air-dried soil samples using a LECO CNS 2000 combustion analyzer (LECO Corp., St. Joseph, MI). Soil concentrations of available P and K were determined using the Bray P1 (Kuo, 1996) and the NH4C2H3O2 (Helmke and Sparks, 1996) methods, respectively. Soil pH was determined from a 2:1 mixture of deionized water and soil, using a pH meter equipped with a glass combination pH electrode.

Field-moist soil samples collected before 15N application were thawed and then wet-sieved to pass through a 2-mm screen. Ammonium N and NO3–N concentrations were determined by extracting a portion of the sample with 2 M KCl using a 1:10 mass ratio of soil to KCl solution (Mulvaney, 1996). A 15-mL aliquot of the KCl extract was analyzed for NH4–N and (NO3 + NO2)-N by steam distillation (Mulvaney, 1996). Labeled soil samples were prepared and extracted in the same way as were nonlabeled samples, with additional precautions to prevent cross-contamination between samples. To collect an adequate amount of N (50 µg N) to allow reliable N isotope analyses, a 50-mL aliquot of each 15N-labeled KCl extract was analyzed for total mineral N (NH4 + NO3 + NO2) using mason-jar diffusion techniques (Mulvaney et al., 1997). Total N in 15N-labeled soil samples was determined by digesting approximately 1 g of field-moist soil using the reduced Fe-permanganate modification of the semimicro Kjeldahl procedure described by Bremner (1996). After the digests had cooled, each was diluted to a volume of 25 mL with deionized water and mixed. A 10-mL aliquot of each diluted digest was then analyzed for total Kjeldahl N (TKN) using mason-jar diffusion techniques (Stevens et al., 2000). The NH3 liberated by diffusion of soil extracts or TKN digests was quantified using an automated titrator (Model 719 S Titrino, Metrohm, Herisau, Switzerland) equipped with a microelectrode (Model MI-411 S, Microelectrodes, Inc., Bedford, NH). Finally, 50 to 200 µg of N from each sample was transferred to a plastic microplate, dried, and analyzed for 15N using a mass spectrometer equipped with an automated Rittenberg apparatus (Mulvaney, 1993). Nonmineral N, which includes both organic N and nonexchangeable NH4–N, was calculated by subtracting mineral (inorganic) N from TKN. The resulting fraction is referred to hereafter as KMI (Kjeldahl minus inorganic) N as per Sanchez and Blackmer (1988).

Experimental Design and Statistical Analysis
The experiment was conducted as a randomized complete block design with three replications. Statistical analysis was accomplished using the SAS GLM procedure (SAS Inst., 1998). Data collected from multiple soil depths within a given experimental unit were considered repeated measures and were analyzed as a split-plot arrangement of a randomized complete block design with N application rate as the main plot and depth as the split plot (Gomez and Gomez, 1984). Differences among treatment means were separated using the Fisher's least significant difference procedure.


    RESULTS AND DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 
Conditions Before 15N Application
The amount of total mineral N (NH4 + NO3 + NO2) in the surface 30 cm of the soil profile before application of labeled N did not vary significantly with N fertilizer application rate within any of the 3 yr (Fig. 2) . In 1995 and 1996, significantly more mineral N was detected in the lower profile (60 to 120 cm) of plots receiving 201 or 268 kg N ha–1 than at the same depth in plots receiving the lower application rates. No such difference was observed in 1994, presumably because unusually wet weather in 1993 (Fig. 3) had flushed residual NO3–N from the profile. The relatively high NO3–N concentrations of 7 to 13 mg kg–1 at the 90- to 120-cm depth in 1995 and 1996 indicate there was some downward movement of NO3–N, but total precipitation was inadequate to remove excess residual N from plots receiving the higher amounts of N fertilizer. Long-term N fertilizer treatment had no significant effect on total N content (Table 1).



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Fig. 2. Distribution of total mineral N (NH4 + NO3 + NO2) by soil depth before spring N application. Each data point represents a mean mineral N concentration for the corresponding soil depth increment (0 to 15, 15 to 30, 30 to 60, 60 to 90, or 90 to 120 cm). Error bars show the LSD (P < 0.05) for mean comparisons within a depth increment. NS indicates differences were not significant.

 


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Fig. 3. (a) Monthly average precipitation (crosshatched bars) and (b) monthly average air temperature (solid bars) recorded at the University of Illinois Northwest Research Center during the year preceding (1993) and 3 yr during which the experiment was conducted (1994–1996). The solid lines show the 100-yr average (a) precipitation and (b) air temperature for Monmouth, IL

 

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Table 1. Effect of long-term N rate on chemical characteristics of a Muscatine soil (surface 15 cm; spring 1994) under continuous corn production at Monmouth, IL.

 
These results would give no reason to vary N fertilizer recommendations based on preplant soil NO3 levels, unless residual NO3–N below 30 cm is considered. This is consistent with the conclusions of Brown et al. (1993), who suggested that a preplant soil NO3 test is of little value for predicting N fertilizer needs in Illinois. In Wisconsin, Motavalli et al. (1992) observed more residual NO3–N in the lower soil profile with higher long-term N application rates than with lower rates, but differences within the top 30 cm were not significant.

First Growing Season after 15N Application
In each of the 3 yr, little fertilizer-derived mineral N remained in the 120-cm profile following harvest when the long-term N fertilizer application rate was either 67 or 134 kg N ha–1 (Table 2). Significantly more labeled mineral N was recovered from plots receiving the two highest N treatments, with 11.4 to 15.3 kg N ha–1 recovered from plots receiving 201 kg N ha–1 and 23.2 to 43.9 kg N ha–1 recovered from those receiving 268 kg N ha–1. This same trend is evident in total mineral N data. With the exception of 1996, total mineral N content did not differ significantly among plots receiving 0, 67, or 134 kg N ha–1 (Table 2). However, more residual mineral N was detected in plots receiving 201 or 268 kg N ha–1 than in those receiving a lower N rate.


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Table 2. Fertilizer- and soil-derived N recovered from the 120-cm soil profile after harvest in the first growing season after application of labeled N.

 
Grain yield data from 1983 to 1996 show that the average agronomic optimum N rate for the Monmouth long-term study is 186 kg N ha–1 (Stevens et al., 1997). This is consistent with the results of the present study as significant residual mineral N accumulated in the soil profile only when this average optimum N rate was exceeded. However, the increased amount of residual NO3–N with the two highest N treatments cannot be attributed entirely to an increase in fertilizer-derived mineral N. In all 3 yr, significantly more soil-derived (unlabeled) mineral N was observed with plots receiving 201 or 268 kg N ha–1 than with plots receiving 67 or 134 kg N ha–1 (Table 2). This added N interaction might be explained by the process of pool substitution, whereby the microbial activity responsible for immobilization of the labeled N also resulted in the mineralization of soil N (Jenkinson et al., 1985). If this were the case, increasing the N fertilizer application rate would be expected to promote greater immobilization of labeled N, yet in 1994, there were no significant differences in recovery of fertilizer-derived N in the KMI-N fraction, which includes both organic and clay-fixed N forms (Table 2). Significant differences in fertilizer-derived KMI-N were observed among N treatments in 1995 and 1996, but the magnitude of those differences was insufficient to account for the 35 to 125 kg ha–1 increases in soil-derived mineral N observed for the 201 and 268 kg N ha–1 plots. This is particularly evident in 1996 when 123 kg ha–1 more soil-derived mineral N was recovered from plots receiving 268 kg N ha–1 than from those receiving 67 kg N ha–1, yet the corresponding increase in fertilizer-derived KMI-N was only about one-third as much.

A more likely explanation is that plots with a history of high N fertilizer application accumulated a larger pool of easily released KMI-N than plots with a history of suboptimal N fertilization. Both organic-matter (Shen et al., 1989) and clay-fixed N pools (Mengel and Scherer, 1981; Norman and Gilmour, 1987) have been shown to release significant amounts of N to the plant-available pool during the growing season. While our data do not allow the separation of residual mineral N into organic-matter- or clay-derived fractions, other researchers have shown evidence that the amount of N fertilizer applied in previous years significantly affects net mineralization of organic N compounds in subsequent growing seasons (Motavalli et al., 1992; Shen et al., 1989). Conversely, Li et al. (1990) observed that release of clay-fixed NH4–N was the same whether a prior urea application was 0 or 70 kg N ha–1. Thus, it is likely that variation in the release of soil-derived N in our study is primarily the result of differences in organic N mineralization.

It is evident from the postharvest distribution of mineral N within the 120-cm soil profile that downward movement did occur (Fig. 4) . No labeled mineral N was detected at the 90- to 120-cm depth during the exceptionally favorable growing season of 1994, but trace amounts were detected in 1995 and 1996 with N fertilizer application rates of 201 or 268 kg N ha–1. Regardless of N rate, trace amounts of fertilizer-derived KMI-N were also detected at profile depths of 60 to 90 cm and 90 to 120 cm, but the majority of the fertilizer-derived KMI-N was recovered from the top 15 cm of plots receiving 67 or 134 kg N ha–1 and from the top 30 cm of plots receiving 201 or 268 kg N ha–1 (data not shown). This suggests that, although some movement of fertilizer-derived N deep into the root zone may have occurred, it is unlikely that significant amounts of labeled N were lost from the rooting zone through leaching during the first growing season. Conversely, with the exception of 1994 when growing conditions were exceptional, significant amounts of total mineral N were detected throughout the profile of the plots receiving 201 and 268 kg N ha–1 (Fig. 5) , indicating that significant amounts of soil-derived NO3–N, which likely includes both native soil N and N from previous fertilizer applications, were leached from the rooting zone.



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Fig. 4. Distribution of fertilizer-derived mineral N (NH4 + NO3 + NO2) by soil depth following crop harvest. Each data point represents a mean mineral N concentration for the corresponding soil depth increment (0 to 15, 15 to 30, 30 to 60, 60 to 90, or 90 to 120 cm). Error bars show the LSD (P < 0.05) for mean comparisons within a depth increment. NS indicates differences were not significant.

 


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Fig. 5. Distribution of total mineral N (NH4 + NO3 + NO2) by soil depth following crop harvest. Each data point represents a mean mineral N concentration for the corresponding soil depth increment (0 to 15, 15 to 30, 30 to 60, 60 to 90, or 90 to 120 cm). Error bars show the LSD (P < 0.05) for mean comparisons within a depth increment. NS indicates differences were not significant.

 
Second Growing Season after 15N Application
When 15N microplots were sampled in the spring of the second growing season, the amount of fertilizer-derived mineral N (Fig. 6b and 7b) was approximately the same as for the previous fall (Fig. 6a and 7a) in plots that had received 67 or 134 kg N ha–1. By comparison, the amount of fertilizer-derived mineral N recovered from plots that had received 201 or 268 kg N ha–1 was only about 50 to 75% of the amount measured the preceding fall. Fertilizer-derived KMI-N increased with increasing N application rate until it reached a plateau at the 201 kg N ha–1 application rate (Fig. 6b and 7b). With the 1994 application of labeled N, from 15.0 to 26.2 kg ha–1 less labeled KMI-N was present in the spring of the second year than in the fall of the first year (Fig. 6) while with the 1995 application, the difference was 3.1 to 14.1 kg N ha–1 (Fig. 7). This may reflect a difference between the 2 yr in mineralization of labeled organic N from both soil organic matter and crop residue. Climatic conditions from November 1994 through March 1995 were warmer and somewhat wetter than for the same period in 1995 and 1996 (Fig. 3). This may account for the apparent net mineralization and loss of 15N with the 1994 application (Fig. 6a and 6b) while only small changes were observed with the 1995 application (Fig. 7a and 7b). As was the case the previous fall, the majority of the labeled KMI-N was located in the top 15 cm of the soil profile, with virtually all in the top 30 cm (data not shown).



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Fig. 6. Recovery of labeled fertilizer N from mineral and Kjeldahl N minus inorganic (KMI) N fractions of a 1.2-m soil profile following a 1994 application of 15NH415NO3. Lowercase and uppercase letters are for comparing (P < 0.05) KMI-N and mineral N means, respectively, within a sampling event. Least significant differences (P < 0.05) for comparing mineral N and KMI-N means within a N treatment and across sampling dates are 4 and 13 kg ha–1, respectively. Parenthetical values are standard deviations for their corresponding means.

 


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Fig. 7. Recovery of labeled fertilizer N from mineral and Kjeldahl N minus inorganic (KMI) N fractions of a 1.2-m soil profile following a 1995 application of 15NH415NO3. Lowercase and uppercase letters are for comparing (P < 0.05) KMI-N and mineral N means, respectively, within a sampling event. Least significant differences (P < 0.05) for comparing mineral N and KMI-N means within a N treatment and across sampling dates are 6 and 14 kg ha–1, respectively. Parenthetical values are standard deviations for their corresponding means.

 
In the fall of the second growing season, no significant difference occurred in recovery of labeled mineral N between plots receiving 67 or 134 kg N ha–1, but a significant increase was observed as N fertilizer application increased to 201 or 268 kg N ha–1 (Fig. 6b and 7b), indicating more extensive mineralization of fertilizer-derived organic N with the two highest N application rates than with the lower rates. In most cases, the amount of labeled KMI-N increased from spring to fall regardless of N application rate. The increase was particularly noticeable in plots receiving 268 kg N ha–1 where the increase from spring to fall, when averaged over the 1994 and 1995 15N applications (Fig. 6b and 7b), was 26.2 kg N ha–1. This indicates that plots receiving 268 kg N ha–1 were overfertilized, leaving a large pool of labeled N available for immobilization. The smaller change in labeled KMI-N content from spring to fall in the plots receiving the lower treatment levels suggests that the lower application rates more closely met crop needs during the previous growing season than did the highest rate.

Third Growing Season after 15N Application
In the spring 2 yr following the application of labeled fertilizer N, only trace amounts of labeled N were present in the mineral form, and no significant differences occurred among the four treatment levels (Fig. 6c). These data suggest that residual fertilizer-derived mineral N present in the profile the previous fall (Fig. 6b) had either been flushed from the soil profile by off-season precipitation or immobilized into organic or clay-fixed forms. There were no significant changes in the amount of labeled KMI-N from the fall of the second year to the spring of the third year, except for with the 268 kg ha–1 application rate, which decreased from 74 to 49 kg N ha–1 (Fig. 6b and 6c), presumably owing to mineralization and subsequent loss between the two sampling dates. These differences were not as great as those observed in the 1994–1995 off-season (Fig. 6a and 6b) when climatic conditions were more favorable for N mineralization and loss (Fig. 3). Similar to observations in the previous fall, plots receiving 268 kg N ha–1 contained the most labeled KMI-N in the spring of the third year, followed by those receiving 201 kg N ha–1, while the plots receiving 67 or 134 kg N ha–1 contained the least. While differences among treatments were less clear in the fall of the third yr, the trend in labeled KMI-N content was similar to that observed in the preceding spring (Fig. 6c). This is not surprising given the low concentration of labeled N in the previous year's crop residues. The amount of labeled organic N mineralized was likely less than in the previous growing season because of the stabilization of organic N with time (Shen et al., 1989).

The pattern in labeled mineral N contents across N application rates was similar in the fall of the third year (Fig. 6c) as in the fall of second year (Fig. 6b) though concentrations were less. There was still significantly more labeled mineral N present with the 268 and 201 kg N ha–1 application rates (3.4 and 2.4 kg ha–1, respectively) than with the 67 or 134 kg ha–1 application rates (<1.0 kg ha–1). Thus, even in the third growing season after the application of labeled fertilizer N, a higher percentage of labeled N was being mineralized with the two highest long-term N fertilizer application rates than with the two lowest rates.


    SUMMARY AND CONCLUSIONS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 
Movement of mineral N to the lower depths of the soil profile was significantly greater in cases involving excessive application of fertilizer N. Very little of the fertilizer-derived N moved to the 120-cm depth during the first growing season, but by the spring of the second growing season, there were indications that fertilizer N was being leached from the profile, especially when N applications exceeded plant uptake.

Results also provide evidence that overapplication of fertilizer N on a consistent, long-term basis may lead to an accumulation of readily mineralizable soil organic N compounds in continuous corn production systems. After one growing season, profile concentrations of total mineral N were consistently greater with the two highest treatment levels than in the profiles of the lower treatments. As expected, the amount of fertilizer-derived mineral N in the profile also increased significantly with increasing N application rate, but more than twice as much soil-derived mineral N was present in the profile when the N application rate was 201 or 268 kg ha–1 than when it was 134 kg ha–1 or less. In the fall of both the second and third growing seasons, very little labeled mineral N was detected in the soil profile when the N application rate was 67 or 135 kg ha–1, but significant amounts were still present when the N application rate was 201 or 268 kg ha–1. By the third growing season, these differences had become quite small, indicating that the labeled portion of the organic N pool had begun to stabilize and become more resistant to mineralization. These data suggest that mineralization of residual organic N is promoted when N fertilizer application rates consistently exceed the optimum N application rate on a long-term basis.

These findings emphasize the environmental risk associated with excessive N fertilization and underscore the need for better predictions of N mineralization. In light of the recent work by Mulvaney et al. (2001) and Khan et al. (2001) that potentially mineralizable N may be estimated by a simple soil test for amino sugar N, further research is warranted to determine whether long-term N applications promote the accumulation of this N fraction and thereby reduce crop responsiveness to subsequent N fertilizer applications.


    ACKNOWLEDGMENTS
 
Financial support was provided in part by The Fertilizer Research and Education Committee (FREC) and the Illinois Groundwater Consortium. We gratefully acknowledge Dr. Eric Adee and staff of the University of Illinois Northwest Research and Education Center for field plot maintenance and Jeff Warren and Lisa Gonzini for assistance in collecting and analyzing samples.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 SUMMARY AND CONCLUSIONS
 REFERENCES
 




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The SCI Journals Crop Science Vadose Zone Journal
Journal of Natural Resources
and Life Sciences Education
Soil Science Society of America Journal
Journal of Plant Registrations Journal of
Environmental Quality
The Plant Genome