Reassessing carbon sequestration in the North China Plain via addition of nitrogen
- 1. Key Laboratory of Agricultural Water Resources, Center for Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang 050021 (China)
- 2. Geological Survey of Jiangxi Province, Nanchang 330030 (China)
Description
Soil inorganic carbon (SIC) exerts a strong influence on the carbon (C) sequestered in response to nitrogen (N) additions in arid and semi-arid ecosystems, but limited information is available on in situ SIC storage and dissolution at the field level. This study determined the soil organic/inorganic carbon storage in the soil profile at 0–100 cm depths and the concentration of dissolved inorganic carbon (DIC) in soil leachate in 4 N application treatments (0, 200, 400, and 600 kg N ha−1 yr−1) for 15 years in the North China Plain. The objectives were to evaluate the effect of nitrogen fertilizer on total amount of carbon sequestration and the uptake of atmospheric CO2 in an agricultural system. Results showed that after 15 years of N fertilizer application the SOC contents at depths of 0–100 cm significantly increased, whereas the SIC contents significantly decreased at depths of 0–60 cm. However, the actual measured loss of carbonate was far higher than the theoretical maximum values of dissolution via protons from nitrification. Furthermore, the amount of HCO3− and the HCO3− / (Ca2+ + Mg2+) ratio in soil leachate were higher in the N application treatments than no fertilizer input (CK) for the 0–80 cm depth. The result suggested that the dissolution of carbonate was mainly enhanced by soil carbonic acid, a process which can absorb soil or atmosphere CO2 and less influenced by protons through the nitrification which would release CO2. To accurately evaluate soil C sequestration under N input scenarios in semi-arid regions, future studies should include both changes in SIC storage as well as the fractions of dissolution with different sources of acids in soil profiles. - Highlights: • The SOC contents significantly increased after long-term nitrogen application, while SIC decreased. • The measured loss of carbonate was far higher than the theoretical values of dissolution from nitrification. • HCO3− / (Ca2+ + Mg2+) ratio in soil solution was higher after N application for the 0–80 cm depth.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2016.04.115Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2016.04.115;
- PII
- S0048-9697(16)30810-5;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 563-564
- Journal Page Range
- p. 138-144
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48011279
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- CARBON; CARBON DIOXIDE; CARBON SEQUESTRATION; CARBONATES; CARBONIC ACID; CHINA; CONCENTRATION RATIO; COST; DISSOLUTION; ECOLOGICAL CONCENTRATION; ECONOMICS; ECOSYSTEMS; FERTILIZERS; LEACHATES; MAGNESIUM IONS; NITRIFICATION; NITROGEN; SILICON CARBIDES; SOILS; UPTAKE
- Descriptors DEC
- AIR POLLUTION CONTROL; ASIA; CARBIDES; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; CONTROL; DIMENSIONLESS NUMBERS; DISPERSIONS; ELEMENTS; HOMOGENEOUS MIXTURES; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; IONS; MIXTURES; NONMETALS; OXIDES; OXYGEN COMPOUNDS; POLLUTION CONTROL; SEPARATION PROCESSES; SILICON COMPOUNDS; SOLUTIONS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.