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a Dep. of Land, Air and Water Resources, Univ. of California, Davis, CA 95616
b Univ. of California Cooperative Extension, Kearney Agricultural Center, Parlier, CA, 93648
c Dep. of Agronomy and Range Science, University of California, Davis, CA 95616
* Corresponding author (wrhorwath{at}ucdavis.edu)
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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Abbreviations: SMB-N, soil microbial biomass N • SMB-C, soil microbial biomass C • SOM, soil organic matter • WF, winter flooded • NF nonwinter flooded
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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Recently, grain producers in North America and Europe have been required to adopt alternative straw management practices, because burning has raised air pollution concerns (Ocio et al., 1991; Eagle et al., 2000). In California, soil incorporation of crop residues during the fall and shallow flooding of fields during the winter-fallow period has replaced open-field burning. These changes in straw management have prompted a reexamination of N immobization–mineralization dynamics and their effect on N fertility in rice soils. In California, rice straw production is 8 to 10 Mg ha-1, and it contains 50 to 70 kg N ha-1 (Brandon et al., 1995). The traditional practice of burning eliminates 70 to 80% of the C and N held in the straw, crown, and roots (Hill et al., 1999). Most of the straw C and N left after burning remains in the form of noncombusted root, crown, and stubble. Consequently, the change from burning to straw incorporation and winter flooding will likely alter the cycling of C and N in soil.
Although many studies have reported the fate of added 15N-labeled fertilizer N in lowland rice agroecosystems, most investigations were limited to the measurement of total fertilizer N in the plant and recovery in the soil (Patnaik and Broadbent, 1967; Patrick and Reddy, 1976; Clement et al., 1995). Few investigations have directly examined the pathways of N immobilization into the microbial biomass (Paul and Juma, 1981). We determined the effects of alternative rice straw management practices on the dynamics of N immobilization of applied fertilizer and crop residue N. 15N stable isotope methodology was used to follow the turnover of added fertilizer and crop residue N in the inorganic, microbial, and total soil and plant N pools. A 2-yr study of 15N fertilizer and crop residues was initiated in a 4-yr-old rice straw management experiment. Our main objective was to assess the effects of straw incorporation and winter flooding on crop N availability, microbial N use-efficiency, and the stabilization of added fertilizer-N and crop residue N in the soil. These parameters are critical to develop straw management practices that lead to an optimization of long-term N supply in flooded soils.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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Straw management practices were implemented following grain harvest in late October 1993. The harvester-combine chopped the rice residue at a height of 7 to 12 cm above the soil surface. The rice straw remaining after harvest averaged 9.5 Mg ha-1. The straw was incorporated by swathing, forage chopping, and stubble disking to a 12-cm depth. The straw was burned by ignition of dry straw with a torch. After the straw was burned, the unburned roots, crown and stubble were left undisturbed. Winter flooding to a depth of 15 cm occurs after fall tillage in November and the fields are drained in early March prior to field preparation. Traditionally, rice soils in California had only undergone submergence during the growing season and remained fallow during the rainy winter months. Unless fields are winter flooded, precipitation during the winter months results in frequent wet and dry periods. Spring tillage operations for all treatments included chisel plowing, disking, and rolling prior to flooding to 15 cm during the growing season (May–September). Fertilizer N was applied prior to aerial seeding as aqua ammonia at rates of 167 and 146 kg N ha-1 in 1997 and 1998, respectively. Triple-super phosphate was applied at a rate of 32 kg P ha-1 in both 1997 and 1998. The fields were maintained with commercial equipment and conventional weed, disease, and insect control management practices.
15N Fertilizer Study
We used 15N to examine the dynamics of fertilizer over a 2-yr period (May 1997–1999). Microplots (4 by 3 m) were established in each main plot prior to the fourth growing season of the field study (May 1997). Enriched urea fertilizer (9.99% 15N-atom excess) was uniformly applied to the microplots at a rate of 20 kg N ha-1 prior to seeding in 1997. The total amount of excess 15N added was 2 kg N ha-1. To reduce losses of applied N during the few days prior to flooding, N-Serve 24-E [nitrapyrin: 2-chloro-6-(trichloromethyl) pyridine; Dow-Elanco, Indianapolis, IN] was applied with the N fertilizer at a rate of 0.4 L ha-1. Immediately following 15N application, the microplots were tilled to a depth of 12 cm. To reduce lateral flow and dilution of the applied fertilizer N, metal barriers were placed around the plot exterior to a depth of 30 cm. Additional unlabelled urea-N fertilizer was applied to the 15N-microplots at a rate of 167 and 146 kg N ha-1 prior to planting in May 1997 and 1998, respectively.
In 1997 and 1998, straw incorporation in the 15N microplots was achieved using a small-scale chopper and tiller that simulated field-scale operations; it conserved the integrity of the microplots. All other agronomic operations applied to the microplots, including annual spring tillage and fertilizer applications, utilized commercial, field-scale equipment.
Instead of burning 15N-labeled straw after the first growing season of the 15N study (1997), the labeled surface straw from the burned plots (straw cut 7–12 cm above the soil surface) was replaced with equivalent amounts of unlabeled rice straw from the adjacent area. The labeled roots, crowns, and stubble along with the unlabeled surface straw in the designated burned plots were then burned. The labeled straw removed from the burned 15N microplots was used for an accompanying study examining the fate of straw N described below. In 1998, labeled surface straw in the burned plots was not removed and was burned.
15N Straw Residue Study
We applied 15N-labeled straw to new microplots to examine the fate of rice straw N. Following harvest in October 1997, the 15N-labeled rice straw from the burned treatment microplots was transferred onto new 15N microplots (4 by 3 m) located in the winter-flooded and unflooded incorporated plots. The labeled surface straw and unlabelled stubble, crowns and roots were incorporated as described for the labeled N fertilizer microplots. The labeled straw applied contained 51.1 kg N ha-1, 3615 kg C ha-1, and had a mean 15N atom excess of 0.434%. The total amount of excess 15N added was 0.221 ± 0.005 kg 15N ha-1. Agronomic operations for the new straw residue microplots were similar as described earlier for the straw management study. The labeled 15N straw was followed for 1 yr . Recovery of the added 15N straw in the different soil N pools was related to the total amount of 15N applied straw N.
Soil Characterization
Prior to the initiation of the field study, selected physical and chemical soil properties were determined. Values were determined on soil sub-samples from a combined soil sample representing the multiple cores from the 0- to 15-cm depth (Table 1). Soil was extracted for exchangeable K, Ca, and Mg with 0.5 M NH4COOH (Knudsen et al., 1982; Lanyon and Hearld, 1982) and subsequently quantified by atomic absorption/emission spectrometry. Plant-available P (Olsen P) was determined by the sodium bicarbonate method (Olsen and Sommers, 1982). Soil pH and electrical conductivity (EC) were measured as a saturated soil paste (Richards, 1954). Soil cation exchange capacity (CEC) was determined by barium acetate saturation and calcium replacement (Janitzski, 1986). Soil particle size distribution was measured in soil suspension by the hydrometer method (Gee and Bauder, 1979). Total soil C and N were measured with a CHN gas analyzer (Nelson et al., 1982). Soil chemical data listed in Table 1 are expressed as concentrations, as soil bulk density was not measured in 1993.
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Microbial biomass C and N were determined by a modified version of the chloroform-fumigation incubation method (10-d chloroform period on saturated soil, Horwath and Paul, 1994). Soil microbial biomass C (SMB-C) was calculated without use of the control and adjusted by a KC value of 0.41 (Voroney and Paul 1984; Horwath et al., 1996). Soil microbial biomass N (SMB-N) was calculated after subtracting the initial extractable soil NH+4. SMB-N values were adjusted by a KN value of 0.57 (Jenkinson, 1988). Carbon dioxide concentrations evolved at the end of the 10-d incubation of the microbial biomass samples were measured with an infrared gas analyzer.
Field moist soil subsamples were extracted with 2 M KCl for exchangeable inorganic N (5:1 extractant:dry soil ratio). Inorganic N was quantified colorimetrically with an automated N analyzer (LACHAT, Mequin, WI) (Keeney and Nelson, 1982). Gravimetric water content was determined by drying soil subsamples at 105°C for 24 h. Total soil C and N were measured as previously described. For 15N analysis, inorganic N and microbial biomass extracts were diffused onto Whatman DF/A filter paper by the teflon filter-pack method on the basis of Stark and Hart (1996). The 15N content of total soil N, extractable inorganic NO-3 and NH+4 and microbial biomass N was determined on a Europa Scientific Integra Mass Spectrometer (PDZ Europa Ltd., Crewe, UK). Soil C and N determinations are expressed on a volumetric basis for data gathered from 1997 to 1999. All soil determinations are expressed on a dry soil basis.
Plant Analyses
In 1997 and 1998, rice plant samples were collected from the 15N-microplots by cutting plants just above the soil surface in two 0.25-m2 quadrats. Grain and straw dry matter were determined after drying samples until constant weight at 60°C and separating into grain and straw biomass. Dried straw sub-samples were ground using a Wiley mill fit with a 2-mm screen; grain and straw subsamples were ball milled to pass a 250-µm sieve. Total C, N, and 15N content were determined as previously described. All plant determinations are expressed on a dry-matter basis.
Statistical Analysis
Main effects of winter flooding and straw management were tested by a general linear model (GLM) designed for the split-plot design. The winter flooding x replicate mean square error (3 df) was used as the error term in the GLM for the winter flooded versus the no winter flood treatments (1 df). The replicate x winter flood x straw management mean square error (6 df) was used as the error term in the GLM for the burned versus incorporated straw treatment (1 df) and the winter flood x straw management interaction (1 df). All data are expressed as least squares means with standard errors of indicated treatments. F statistics and P values are indicated in text and tables for all GLM procedures. A significance level of P < 0.05 was set a priori as the 
-level; and P values were specified between 0.05 and 0.20 in tables and text to facilitate data interpretation. P values greater than 0.20 are indicated simply as NS (nonsignificant) in the tables. Adjusted Bonferroni t-tests were performed between soil inorganic N and microbial biomass N data to compare 15N atom excess values on specific sample dates. The kinetic parameters of So (initial substrate concentration) and k (decay rate) for microbial biomass fertilizer recovery were derived by fitting the recovery of 15N fertilizer as SMB-15N to a single exponential model (Eq. [1]).
 | (1) |
Time is expressed in years. Kinetic parameters were derived for each plot (N = 16) by the Non-linear procedure in SYSTAT version 7.0 (1997, SPSS Inc., Chicago, IL). Parameters from each plot were then used to test main effects by GLM procedures described previously. Means and standard errors of So and k for each treatment (N = 4) are presented. All statistical tests were performed using SYSTAT version 7.0.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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Total fertilizer 15N recovery in the 0- to 15-cm soil depth was similar among treatments during the first growing season of the 15N fertilizer study and averaged 29% at crop maturity in August 1997 (Fig. 1). Following rice harvest in 1997, soil recovery of applied fertilizer 15N increased in all plots 14 d after straw incorporation and burning. In May 1998, fertilizer 15N recovery in the soil after the winter fallow period was greater when straw was incorporated compared with the amount of 15N recovered with straw burned (F = 5.68; P = 0.054). From that applied in May 1997, the amount of residual 15N fertilizer recovered in the soil averaged 14.9% after the 1998 growing season (September) and 14.1% after the second winter fallow season (May 1999). Although more 15N in the soil 0- to 15-cm depth was recovered after 2 yr (May 1999) when straw was incorporated, this difference was not statistically significant (F = 1.99; P = 0.208). Winter flooding did not affect total 15N recovery in the top 15-cm of the soil during the 2-yr 15N-study period.
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Soil Extractable Inorganic N
Inorganic N (NO-3 and NH+4) during the 2-yr 15N study was relatively low and ranged from 25.4 to 1.5 kg N ha-1 (Fig. 2). Ammonium was the dominant inorganic N form extracted during flooded periods. Nitrate was present at amounts greater than 0.2 kg N ha-1 during the seasonal dry periods in the fall (November), spring (May) and winter (nonwinter flooded) and was the dominate form of inorganic N only at preplanting (May 1998 and 1999). Highest inorganic N values were observed during mid-season in July 1997 and prior to planting in May 1998 and 1999. Compared with nonwinter-flooded conditions, inorganic N contents increased under winter flooded conditions when straw was burned and incorporated (Fig. 2). Increases in inorganic N due to winter flooding occurred prior to the growing season (May) in both years of the fertilizer study compared with nonwinter flooded (Table 3). Additionally, winter flooding led to significantly higher inorganic N levels during mid-season (July 1997) and prior to the winter fallow in November 1998. Two weeks after straw incorporation in November 1997, inorganic N in incorporated plots was less than the inorganic N content in the soil when burned. In November 1998, both burned and incorporated treatments had low inorganic N contents. Slightly greater inorganic N was present in the top 15 cm of soils in incorporated plots versus burned prior to planting (May 1998) and during the growing season in September 1998 (Fig. 2).
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Over the 2-yr 15N-fertilizer study, no significant differences were detected among straw management treatments for the 15N-atom excess values of the SMB-N (data not shown). In July 1997, 22.8% of the N in the microbial biomass was from the N fertilizer. At this stage, winter flooding led to an increase in the recovery of fertilizer-N in the SMB-N as compared with nonwinter flooding: 12.1 ± 1.3% and 8.5 ± 0.6%, respectively (F = 9.4; P = 0.054). Initial amounts of 15N immobilization were similar when straw was incorporated or burned in July and August 1997. In fall (November 1997) and spring (May 1998), the recovery of SMB-15N was greater when straw was incorporated than when burned (fall: F = 4.0; P = 0.093; spring: F = 12.0; P = 0.013). Four months after 15N-fertilizer application (September 1997), about one-quarter of the 15N remaining in the soil was immobilized in the SMB-N. Averaged across treatments, the percentage of 15N-fertilizer in the soil that was present in the SMB-N decreased to 10% in September 1998 and became 18.8% 2 yr after 15N fertilizer application (Table 4). Overall, during the second growing season of the 15N-fertilizer study (1998) the amount of 15N in the microbial biomass was not affected by straw management.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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In this study, straw incorporation increased plant available soil N supply compared with straw burning after the straw was incorporated for 3 yr (Eagle et al., 2000). When rice was grown without any additional fertilizer-N in annual trials, grain yield and total N accumulation almost doubled when straw was incorporated. This effect of yield and N uptake was seen annually after the third season of treatments (Eagle et al., 2000). Additionally, in the absence of N fertilizer, winter-flooded treatments with straw retained resulted in greater yields and N uptake than those not winter flooded with straw retained in Years 3 and 4 of the field study. However, no yield effect was seen at optimum N fertilizer levels among all treatments through Year 6 (Eagle et al., 2000).
Studies directly examining the long-term effects of application of straw compared with burning have reported both positive and negative effects on soil N accumulation, plant-N availability, and yields under tropical conditions. Comparing 5 yr of straw incorporation compared with straw burning, a slightly higher soil organic C, greater inorganic N levels and increased wheat and rice yields were observed (Verma and Bhagat, 1992). In contrast, Beri et al. (1995) reported a yield decline during an 11-yr field study when straw was incorporated even though total soil N increased. Beri et al. (1992) attributed this yield reduction to low available N because this decline was reversed after straw incorporation ceased. While the yield constraints in these studies from the tropics are likely different than under the temperate climate found in California, it appears that long-term straw incorporation can play an active role in providing greater amounts of plant-available N.
Inorganic N in winter-flooded soil was higher than in nonwinter-flooded soil prior to planting, and during the growing season. The large amounts of inorganic N present during July 1997 may be due to the higher N fertilizer rates used in 1997 compared with 1998 when N rates were decrease to more accurately meet crop demand. The increase in inorganic N in winter-flooded plots may occur because of the lower N requirement of anaerobic heterotrophs (Acharya, 1935). While most of the differences in inorganic N due to winter flooding were generally small, they may play an important role in plant N nutrition when inorganic N is limiting. Our results indicate greater available N in the both burned and incorporated winter flooded treatments compared with the respective nonflooded treatments.
Straw incorporation, compared with burning, resulted in lower inorganic N in November 1997, thereby conserving N likely to be lost over the winter fallow period. This straw management effect was not observed in November 1998 when inorganic N amounts were low in all treatments. No effect of straw incorporation on inorganic N in November 1998 suggests that N immobilization was occurring in both incorporated and burned straw management treatments. Additionally, straw incorporation increased inorganic N levels in 1998 during the spring and growing season suggesting the release of immobilized N to the crop. The effects of straw incorporation on inorganic N are consistent with other work that showed a brief period of N immobilization followed by a subsequent increase in N mineralization (Rule et al., 1991; Nishio et al., 1993).
Sustained, higher SMB-N and SMB-C were observed after 4 yr of straw incorporation. Changes in the C content of the microbial biomass have been promoted as an early indicator of changes in the soil organic matter status and fertility from long-term in situ straw incorporation studies (Powlson and Jenkinson, 1981). Laboratory investigations using continuous applications of rice straw compared with straw removal, showed temporal increases in SMB-N and SMB-C, which in general, declined over time (Azmal et al., 1997; Devêvre and Horwath, 2000). Continuous applications of crop residues appear to be necessary to sustain higher SMB-N and SMB-C (S
renson, 1987; Dalal et al., 1990). Long-term incorporation of straw (18 yr) showed greater SMB-N (50 and 46%) and SMB-C (45 and 37%) than when barley straw was burned (Powlson et al., 1987). For these reasons, the greater sustained microbial biomass levels in incorporated plots compared with burned suggest a larger active C and N pool.
15N Fertilizer and Straw Residue Dynamics
The use of 15N-labeled fertilizer during the fourth and fifth year of the field study enabled us to follow the fate of fertilizer N as affected by changes in rice residue management implemented in 1993. As expected, soil microbial biomass and inorganic N pools were the most enriched soil N pools; however, the size of these pools were small illustrating their dynamic nature. At the time of maximum plant N uptake following 15N addition (July 1997), most of the fertilizer N remaining in the soil was organic (90%). In September 1997, grain uptake of fertilizer N was greater in the burned plots than incorporated, whereas total grain-N uptake (fertilizer and native soil N) was similar among treatments (Eagle, 2000). These results suggest that in incorporated plots, there was greater immobilization of fertilizer N by the soil microbial biomass with a concurrent greater mineralization of native soil N. However, our results also show similar amounts of fertilizer N in microbial biomass and inorganic N pools in the incorporated and burned treatments at both sampling times during the first growing season after 15N application. Therefore, the net result is a greater loss of fertilizer N from the incorporated treatments than the burned by the end of the 1997 growing season. This loss was offset by greater fertilizer N retained in the soil after fall straw incorporation in May 1998 in incorporated plots compared with burned.
Straw incorporation resulted in greater total soil recovery (0–15 cm) of fertilizer N prior to planting 1 yr after 15N application (May 1998), and more 15N as available N in September 1998. Similarly, grain uptake of residual fertilizer N in 1998 was slightly greater in incorporated plots than in burned (Table 2; Eagle, 2000). Increased retention of N in the incorporated plots contributed to increased plant-N availability in the second crop cycle of the fertilizer 15N study. Results from the additional microplot study, assessing the contribution of straw-N to immobilization of fertilizer N, suggest that slightly more than half (62%) of the increase in total 15N immobilization in incorporated plots over the burned in May 1998 was due to fall incorporated straw. These results suggest a significant contribution of the unburned straw stubble-N and root-N to soil N immobilization over the winter fallow period in incorporated plots. This may be due to the incorporation of straw in the top 15 cm of the soil compared with the no-till winter fallow in burned plots.
Our results support the active role of the microbial biomass in competing for added fertilizer in flooded rice soils in all rice straw management systems evaluated here. Microbial biomass accumulated 23% of its N with fertilizer N by mid-season (10.2% of added fertilizer). Similar findings were reported from a field study with wheat where microbial biomass accounted for 30% of the N retained in the soil (18.1% of added) at the end of the first growing season (Paul and Juma, 1981). The large amount of N immobilized by the soil microbial biomass in our study may be due to a preference for the dominant form of inorganic N (NH+4) by heterotrophic bacteria found in flooded soils and the lower loss potential of NH+4 compared with NO-3 (Jenkinson et al., 1985). In addition, the larger microbial biomass in the straw incorporated plots led to an increase in N immobilization. For these reasons, our study emphasizes the importance of soil microbial biomass in controlling fertilizer N sequestration and subsequent availability in flooded rice soils in California. Overall, the long-term effects of a greater biomass along with a larger organic soil N additions appear positive because greater N immobilization of fertilizer N in the incorporated plots was more than offset by greater remineralization of previously immobilized and native soil N.
The turnover of immobilized fertilizer N in microbial biomass was described by first-order decay model 2 yr following fertilizer application. However, the first-order model poorly accounted for the pulse of 15N entering the microbial biomass as straw-N in the fall. The calculated half-lives of 200 to 300 d for immobilized 15N in the soil microbial biomass are similar to those reported by Paul and Juma (1981). They calculated a half-life of 180 d for N immobilized in the microbial biomass during a laboratory incubation of 15N-labeled soil after one growing season. As expected the rate of turnover of 15N immobilized by the soil microbial biomass was faster than the total loss of 15N from the soil, illustrating the stability of more than 50% of the immobilized 15N in soil organic matter pools.
The turnover of assimilated fertilizer N in crop residues is evident in the large increase in soil 15N enrichment from crop maturity to late fall (November 1997) regardless of treatment. Much of the straw at this time was not decomposed and was present in large pieces (>2 mm). Therefore, the most likely sources of this steep increase in recovered fertilizer N in the soil were N released from straw and root turnover. Although not measured directly, turnover of 15N immobilized by algae may have contributed to this steep increase in enrichment in the fall after drainage. Floodwater algae have been found to immobilize up to 40% of 15N-labeled urea applied to greenhouse pots (Vlek et al., 1980).
The total 15N budget 2 yr after 15N fertilizer application shows no significant differences in N losses, and about half of the applied 15N was unaccounted for across all treatments in the plant-soil system. Most studies report 15N recovery and losses at the end of the first cropping season resulting in few examples of losses after one or 2 yr of cropping and fallow (Vlek and Byres, 1986). Our fertilizer 15N loss from the plant-soil (0–15 cm) system after one season (August 1997) averaged 35.8% across treatments. Similar losses were reported for urea (25–30%) in rice (Craswell et al., 1985; Bronson et al., 2000). The two most significant periods of potential N loss from the soil-plant system occur during the spring tillage operation and just after application of the fertilizer. Following the fertilizer application, all treatments were flooded for the growing season. During this initial crop growth period, a rapid and large amount of applied N can be lost the via denitrification and volatilization processes (Vlek and Byrnes, 1986). During the spring, drying, tillage, and higher temperatures increase N mineralization and the conversion of NH+4 to NO-3, which will subsequently be lost during dry-down and upon subsequent flooding. A higher amount of 15N fertilizer recovered in the subsoil (15- to 90-cm depth) in the nonwinter flooded plots compared with winter-flooded at the end of 2 yr (May 1999), suggests that greater denitrification activity (especially in the 15- to 30-cm depth) may be present in winter-flooded subsoils. This trend observed in the subsoil N loss due to winter flooding, however, was not apparent in the topsoil over the 2-yr period (1997–1999). While the overall loss fertilizer N after 2 yr, considered alone, reveals little information about the effects of straw management practices on fertilizer N utilization, the flux of N through the biomass, inorganic-N, and plant-N pool suggests that a labile pool of available N has been produced with 4 to 6 yr of straw incorporation compared with burned. This soil N pool is released during crop growth and offsets the lower fertilizer- N use efficiency of rice observed in incorporated plots during Year 1.
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CONCLUSIONS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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ACKNOWLEDGMENTS |
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Received for publication June 22, 2000.
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REFERENCES |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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renson, L.H. 1987. Organic matter and microbial biomass in a soil incubated in the field for 20 years with 14C-labelled barley straw. Soil Biol. Biochem. 19:39–42.This article has been cited by other articles:
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  N. H. Thuy, Y. Shan, Bijay-Singh, K. Wang, Z. Cai, Yadvinder-Singh, and R. J. Buresh Nitrogen Supply in Rice-Based Cropping Systems as Affected by Crop Residue Management Soil Sci. Soc. Am. J., February 15, 2008; 72(2): 514 - 523. [Abstract] [Full Text] [PDF]
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 B. A. Linquist, S. M. Brouder, and J. E. Hill Winter Straw and Water Management Effects on Soil Nitrogen Dynamics in California Rice Systems Agron. J., June 5, 2006; 98(4): 1050 - 1059. [Abstract] [Full Text] [PDF]
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J. A. Bird, C. van Kessel, and W. R. Horwath Stabilization of 13C-Carbon and Immobilization of 15N-Nitrogen from Rice Straw in Humic Fractions Soil Sci. Soc. Am. J., May 1, 2003; 67(3): 806 - 816. [Abstract] [Full Text] [PDF]
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J. A. Bird, C. van Kessel, and W. R. Horwath Nitrogen Dynamics in Humic Fractions under Alternative Straw Management in Temperate Rice Soil Sci. Soc. Am. J., March 1, 2002; 66(2): 478 - 488. [Abstract] [Full Text] [PDF]
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A. J. Eagle, J. A. Bird, J. E. Hill, W. R. Horwath, and C. van Kessel Nitrogen Dynamics and Fertilizer Use Efficiency in Rice following Straw Incorporation and Winter Flooding Agron. J., November 1, 2001; 93(6): 1346 - 1354. [Abstract] [Full Text] [PDF]
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