Nitrogen Fertilizers and N2O Emissions

1Lemke,R.L., 2Lafond,G., 3Brandt, S., 4Malhi, S.S., and 5Farrell, R.

1Semiarid Prairie Agricultural Research Centre, Swift Current; 2Semiarid Prairie Agricultural Research Centre, Indian Head; 3Saskatoon Research Centre, Scott; 4Saskatoon Research Centre, Melfort; 5Saskatchewan Centre for Soil Research, U of S

Introduction

The atmospheric concentrations of nitrous oxide (N2O), carbon dioxide (CO2) and methane (CH4) have been increasing rapidly. We are concerned about this because all three gases absorb long-wave radiation thereby increasing the amount of heat trapped in the earth’s atmosphere. In addition, N2O is involved in the destruction of stratospheric ozone, which shields the earth from biologically harmful ultra-violet radiation. Chlorofluorocarbons (CFCs), used in refrigeration systems, have been the major contributors to ozone destruction. Their recent phase out has not resulted in as rapid a recovery of the ozone layer as had been anticipated. Simulation studies now suggest that the rapid increase in stratospheric N2O is slowing the recovery, and could eventually begin to reverse some of the gains already made.

Canada has responded to these concerns by committing to a significant reduction in greenhouse gas emissions within the next decade. Current estimates suggest that agricultural activities are responsible for 10 to 15 % of Canada’s human-induced greenhouse gas emissions (Neitzert et al. 1999). While CO2 is the major concern for most industries, the main greenhouse gas emitted by the agricultural sector is N2O. Nitrous oxide is emitted directly and indirectly from crop and livestock production systems. Approximately 40% of the direct emissions from crop production systems are associated with the use of nitrogen (N) fertilizers. These estimates are calculated using a methodology derived by the Intergovernmental Panel on Climate Change (IPCC). The IPCC methodology assumes, as a default value, that 1.25 % of applied N is lost directly as N2O (IPCC 1997). No accommodations are made for differing soil or environmental conditions, which are known to strongly influence N2O emissions. In addition, the timing, placement and formulation of N fertilizer may have a significant influence on the amount of N2O emitted. Nitrous oxide emissions from anhydrous ammonia (AA), for example, have been reported to be substantially higher than other N formulations (Eichner 1990). The proposed loss coefficients need to be tested for western Canadian soil and climatic conditions and modified if necessary.

An extensive research project has been undertaken in Saskatchewan to address a number of the major questions regarding N2O loss from N fertilizer use. This presentation will discuss some preliminary results pertaining to four specific questions:

  1. How much N from fertilizers is lost directly as N2O under western Canadian conditions?
  2. Does fertilizer N source (AA vs. urea) influence direct losses of N2O?
  3. Does application time (spring vs. fall) influence direct losses of N2O?
  4. Does fertilizer placement (side-row vs. mid-row band) influence direct losses of N2O?

Study Description

The data presented in this paper is taken from an ongoing study investigating the influence of timing, placement and form of N fertilizer on N2O emissions. Briefly, this study includes field experiments at four locations, Swift Current, Scott, Indian Head and Star City. There are three test crops, canola, flax and wheat, at each site although only measurements made on the wheat crops are presented in this paper. Treatments that will be referred to here consist of urea and anhydrous ammonia (AA) banded in the fall or spring. Spring banded N was placed either to the side of the seed row (side-row band) or midway between alternate crop rows (mid-row band).

Nitrogen fertilizer was applied at 80 kg N ha-1 at Star City and Indian Head, and 60 kg N ha-1 at Swift Current and Scott. All sites received applications of P fertilizer (11-51-0), at rates of 17 kg P2O5 ha-1 at Scott and Swift Current and 23 kg P2O5 ha-1 at Star City and Indian Head. Phosphorus was placed with the seed except for the side-banded urea treatments where both N and P were placed in the side-row band. A blanket treatment of K2SO4 was broadcast prior to seeding at all sites to ensure sufficiency of these nutrients.

Trace gas samples were collected using vented soil chambers as described by Lessard et al. (1994). Sample collection and analysis followed accepted protocols similar to those described by Lemke et al. (1998). Annual estimates of N2O loss are the sum of N2O lost during the growing season plus the following spring thaw period.

Results and Discussion

Indian Head experienced unusually cool temperatures and above average precipitation during May and June of 2000, and somewhat drier than normal conditions for the balance of the season. Star City, Swift Current, and Scott experienced moderately dry conditions during early May, then above average precipitation from mid-May through to late July. Conditions at all sites were dry during the fall of 2000 and the spring of 2001. Overall, the growing season and fall of 2001 were very dry with most locations receiving 65 % or less of their mean long-term precipitation. Similarly, the spring of 2002 was very dry.

Previous studies in western Canada have shown that N fertilizer application generally increases N2O emissions when considered on a "per acre" basis (e.g. Corre et al. 1999, Lemke et al. 1999). Preliminary results from our study confirm these findings, but in our study the differences were frequently not statistically significant. Nitrogen fertilizer increased N2O emissions significantly only at one of four sites (Table 1) in the 2000/2001 season, and at two of three sites in the 2001/2002 season (Table 2). Our results also indicate very little difference in total N2O emissions from the N management systems we compared. Emissions from plots receiving N as AA tended to be slightly higher than those receiving N as urea, however the differences were not statistically significant. Similarly, emissions tended to be higher from mid-row compared to side-row banded N, but statistically significant differences were noted in only two of the six site-years presented. Applying N in the fall seems to increase the risk of N2O emissions during the following spring thaw, but on an annual basis N2O emissions were generally not significantly affected. It should be noted that snow cover during the study period was limited at most sites, which in turn reduced the risk of N2O production during spring thaw. As a consequence, we have limited confidence in the results of the spring vs. fall applied N comparison.

Table 1. Estimated annual N2O loss from selected treatments at four sites in Saskatchewan for the period May 2000 to April 2001.

N-form / Band Placement

Swift Current

Indian Head

Scott

Star City

 

_________________ g N ha-1 ________________

Urea side-row 1

302

114

121

162

Urea mid-row 2

393

186

115

501

Urea banded in fall

340

218

236

672

AA3 side-row

246

200

110

472

AA mid-row

411

140

166

758

AA banded in fall

301

187

194

414

Check (no N)

231

52

85

631

Contrasts

Significance

no N vs. N applied

ns 4

0.02

ns

ns

Fall vs. Spring banded N

ns

ns

ns

ns

Mid-row vs. Side-row

0.06

ns

ns

0.01

AA vs. Urea

ns

ns

ns

ns

1 side-row = fertilizer band placed to one side of the crop row

2 mid-row = fertilizer band placed midway between alternating crop rows

3 AA = anhydrous ammonia

4 ns = not significant (p>0.1)

Table 2. Estimated annual N2O loss for selected treatments at three sites in Saskatchewan

for the period May 2001 to April 2002.

N-form / Band Placement

Swift Current

Indian Head

Scott

 

_________________ g N ha-1 ________________

Urea side-row 1

55

47

46

Urea mid-row 2

163

27

76

Urea banded in fall

39

64

97

AA3 side-row

155

43

76

AA mid-row

159

59

188

AA banded in fall

63

47

127

Check (no N)

27

4

23

Contrasts

Significance

no N vs. N applied

0.03

0.08

ns 4

Fall vs. Spring banded N

0.01

ns

ns

Mid-row vs. Side-row

ns

ns

ns

AA vs. Urea

ns

ns

ns

1 side-row = fertilizer band placed to one side of the crop row

2 mid-row = fertilizer band placed midway between alternating crop rows

3 AA = anhydrous ammonia

4 ns = not significant (p>0.1)

Table 3. Percentage of Fertilizer-N lost as N2O at Four Sites in Saskatchewan for the period May 2000 to April 2001.

N form/Band Placement

Swift Current

Indian Head

Scott

Star City

 

%

Urea side-row 1

0.12

0.08

0.06

-0.59

Urea mid-row 2

0.27

0.17

0.05

-0.16

Urea banded in fall

0.18

0.21

0.25

0.05

AA 3 side-row

0.03

0.19

0.04

-0.20

AA mid-row

0.30

0.11

0.14

0.16

AA banded in fall

0.12

0.17

0.18

-0.27

Mean

0.17

0.16

0.12

-0.17

1 side-row = fertilizer band placed to one side of the crop row

2 mid-row = fertilizer band placed midway between alternating crop rows

3 AA = anhydrous ammonia

We calculated the percentage of N lost as N2O based on our estimates of annual loss. Assuming that N2O loss from the check (no N applied) treatment represents a background emission, then the difference between this background value and the amount of N2O lost from treatments receiving N should represent the "fertilizer induced" N2O emission. That difference divided by the total N applied as fertilizer (x 100) provides an estimate of the percentage of fertilizer N lost as N2O. The values calculated for the 2000/2001 season at four sites are presented in Table 3, and for the 2001/2002 season at three sites are presented in Table 4. The values calculated in our study are considerably lower than the IPCC default value discussed earlier. For example, the highest percent loss estimated was 0.30. This value is approximately 4x lower than the 1.25 % proposed in the IPCC methodology. Emissions from the check treatment at Star City during the 2001 spring thaw period were unusually high, resulting in negative percent loss values being calculated for many of the treatments. We believe this unusual outcome is simply an artifact of the high spatial variability inherent to N2O emissions. Estimates of N2O loss for the Star City site during the 2001/2002 season were not available at the time of writing.

Table 4. Percentage of Fertilizer-N lost as N2O at Three Sites in Saskatchewan for the period May 2001 to April 2002.

N-form/Band Placement

Swift Current

Indian Head

Scott

 

%

Urea side-row 1

0.05

0.05

0.04

Urea mid-row 2

0.23

0.03

0.09

Urea fall banded

0.02

0.08

0.12

AA3 side-row

0.21

0.05

0.09

AA mid-row

0.22

0.07

0.28

AA fall banded

0.06

0.05

0.17

Mean

0.13

0.06

0.13

1 side-row = fertilizer band placed to one side of the crop row

2 mid-row = fertilizer band placed midway between alternating crop rows

3 AA = anhydrous ammonia

Summary

Nitrous oxide loss tended to be higher from field plots receiving N fertilizer compared to plots that didn’t, but the increase was frequently not significant. The management of N fertilizers had very little influence on annual N2O losses in this study. Nitrous oxide emissions from the fall banded treatments was often higher during spring thaw, but lower emissions during the growing season resulted in virtually no significant differences between the fall and spring applied N treatments when compared on an annual basis. However, the lack of snow cover at most sites during the study period limits our confidence in this comparison. Losses from mid-row placed N tended to be higher than side-row placed N, but again these differences were rarely significant. There was no indication that anhydrous ammonia significantly increases N2O emissions relative to urea. We estimated that 0.3 % or less of fertilizer-N was lost as N2O. This value is many times lower than the current factor utilized to estimate N2O loss from fertilizer N in western Canada, suggesting that the current factor needs to be modified. Emissions were low from all the N-management systems investigated, suggesting that the specific N-management system selected is of less importance than how carefully the N is managed.

Acknowledgments

We gratefully acknowledge the financial support provided through the Agriculture and Agri-Food Canada Matching Initiatives Program, Canadian Fertilizer Institute, Saskatchewan Agriculture Development Fund, Bourgault Industries and the Saskatchewan Flax Development Commission, as well as in-kind support from the Prairie Agricultural Machinery Institute, Big Quill Enterprises, Western Ag Innovations, and Flexi-coil Ltd. We wish also to acknowledge the continued efforts of the technical support staff at Scott, Melfort, Indian Head, Swift Current and the Saskatchewan Centre for Soil Research, U of S.

 

References

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