4.6 Article

Relative contributions of bacteria and fungi to nitrous oxide emissions following nitrate application in soils representing different land uses

Journal

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ibiod.2021.105199

Keywords

Nitrogen fertilisation; Nitrous oxide; Antibiotics; Fungi; Bacteria; qPCR

Funding

  1. ERDF
  2. Ministerio de Economia, Industria y Competitividad [AGL2017-85676R]
  3. Federation of European Microbiological Societies (FEMS) [FEMS-RG-2017-0067]
  4. Ministerio de Educacion Cultura y Deporte (MECD) [FPU 2014/01633]
  5. UK Biotechnology and Biological Sciences Research Council (BBSRC) [BBS/E/C/000I0310, BBS/E/C/000I0320, BBS/E/C/000J0100]
  6. UK Natural Environment Research Council (NERC) [NE/M013847/1, NE/M015351/1]
  7. BBSRC [BBS/E/C/000I0310, BBS/E/C/000I0320] Funding Source: UKRI
  8. NERC [NE/M013847/1] Funding Source: UKRI

Ask authors/readers for more resources

This study investigated the contribution of bacteria and fungi to N2O and CO2 production in soil after nitrate application. The results showed that fungi contributed more to N2O emissions initially, while bacteria had a greater impact later on. The use of antibiotics effectively inhibited the growth of bacteria and fungi, highlighting the importance of considering both microbial groups in greenhouse gas mitigation strategies.
Bacteria and fungi have been shown to produce nitrous oxide (N2O) during denitrification, but their contribution after nitrate (NO3? ) application to soil is not clearly established. In a microcosm experiment, the relative contribution of bacteria and fungi to N2O and carbon dioxide (CO2) production by four contrasting soils representing different land uses after KNO3 addition was studied. The soils were daily wetted to 80% water-filled pore space (WFPS) and kept under greenhouse conditions for 10 days. The fungicide cycloheximide and the bactericide streptomycin were used to determine the possible microbial origin of the N2O and CO2 emissions. Non-target effects of the antibiotics on the emission of N2O and CO2 were evaluated using the inhibitor additivity ratio (IAR). The abundance of the bacterial and fungal communities was estimated by quantitative PCR (qPCR) of the bacterial 16S rRNA gene and the fungal internal transcribed spacer (ITS) region, respectively. The gene copy number of bacterial denitrifiers was calculated after quantification of the nirK, nirS, norB, nosZI and nosZII genes. After 10 d, regardless of the soil type, the cumulative N2O emission from the soils treated with cycloheximide or streptomycin were similar. In all the four soils, N2O fluxes were greater (on average 1.8 ? 0.3 times) in soils amended with the fungicide than with the bactericide during incubation for the first 48?96 h. Greater N2O emissions (on average 1.7 ? 0.2 times) were detected in soils where bacteria were inhibited in comparison to those treated with the fungicide from 96 to 240 h. On average, 68.5% of the total CO2 emitted during the 10d incubation period was produced in soils treated with the fungicide and 31.5% in those treated with the bactericide. The greater contribution of bacteria to the production of N2O than fungi during the first 48?96 h was possibly due to a faster used of nitrate. Variations in the abundance of bacterial 16S rRNA genes, the ITS region, and the nirK, nirS, norB and nosZI bacterial denitrification genes indicated that the antibiotics used to prevent the growth of bacteria and fungi were effective during incubation. These results suggest that both bacteria and fungi should be considered when designing and applying greenhouse gas mitigation strategies in soils and that their relative contribution to produce N2O and CO2 can vary with time and nitrate availability.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available