Cailing Shi, Jing Zhang, Haibo Zhang, Lei Xu, Wenjun Xie, Weiming Li, Lichang Zhang and Yu Sun
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Results showed that the straw mineralization rate and the amount of potentially mineralized straw significantly decreased with increasing salinity (<em>p</em> < 0.05). Compared with BS, the cumulative CO<small><sub>2</sub></small> emissions, PE, and the amount of mineralized straw in LS, MS, and HS decreased by 3.6%–26.8%, 3.4%–26.5%, and 2.7%–15.6%, respectively. Simultaneously, increasing soil salinity prompted the earlier occurrence of the peak straw mineralization and PE. The contribution of straw mineralization to CO<small><sub>2</sub></small> emissions on the 1st day significantly decreased with rising salinity levels (<em>p</em> < 0.05), while the opposite change was observed from 5 days to 120 days. Although PE significantly decreased with increasing salinity, the duration of the effect of straw input on soil organic matter mineralization increased substantially in high-salinity soils. These findings reveal the influence of soil salinity levels on the straw mineralization process and CO<small><sub>2</sub></small> emission, which will help us assess and boost carbon sequestration in saline soils under straw input conditions.</p>","PeriodicalId":74,"journal":{"name":"Environmental Science: Processes & Impacts","volume":" 3","pages":" 794-803"},"PeriodicalIF":3.9000,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Straw mineralization and carbon dioxide emissions in soils with different salinity levels\",\"authors\":\"Cailing Shi, Jing Zhang, Haibo Zhang, Lei Xu, Wenjun Xie, Weiming Li, Lichang Zhang and Yu Sun\",\"doi\":\"10.1039/D4EM00698D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Straw application is widely used to reclaim saline soils. 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引用次数: 0
摘要
秸秆被广泛用于盐碱地的复垦。然而,在盐碱地中,秸秆矿化的特征及其诱导启动效应(PE)在很大程度上是未知的。因此,我们进行了180天的盐渍土培养实验,观察秸秆矿化和CO2排放特征。建立了3.0 g kg-1 (BS)、5.0 g kg-1 (LS)、10.0 g kg-1 (MS)和15.0 g kg-1 (HS) 4个盐度水平,其中13c标记玉米秸秆以5.0%的添加率添加。结果表明,随着盐度的升高,秸秆矿化率和潜在矿化秸秆量显著降低(p < 0.05)。与BS相比,LS、MS和HS的累积CO2排放量、PE和矿化秸秆量分别降低3.6% ~ 26.8%、3.4% ~ 26.5%和2.7% ~ 15.6%。同时,土壤盐分的增加使秸秆矿化高峰和PE的出现时间提前。随着盐度的升高,第1天秸秆矿化对CO2排放的贡献显著降低(p < 0.05),第5 ~ 120天则相反。虽然PE随盐度的增加而显著降低,但秸秆投入对土壤有机质矿化影响的持续时间在高盐度土壤中显著增加。这些发现揭示了土壤盐分水平对秸秆矿化过程和CO2排放的影响,有助于我们评估和促进秸秆投入条件下盐碱地的碳固存。
Straw mineralization and carbon dioxide emissions in soils with different salinity levels
Straw application is widely used to reclaim saline soils. However, the characteristics of straw mineralization and its induced priming effects (PE) in saline soil are largely unknown. Thus, we conducted a 180-day saline soil incubation experiment to observe the characteristics of straw mineralization and CO2 emissions. Four salinity levels, i.e., 3.0 g kg−1 (BS), 5.0 g kg−1 (LS), 10.0 g kg−1 (MS), and 15.0 g kg−1 (HS), were established, to which 13C-labeled maize straw was added at a rate of 5.0%. Results showed that the straw mineralization rate and the amount of potentially mineralized straw significantly decreased with increasing salinity (p < 0.05). Compared with BS, the cumulative CO2 emissions, PE, and the amount of mineralized straw in LS, MS, and HS decreased by 3.6%–26.8%, 3.4%–26.5%, and 2.7%–15.6%, respectively. Simultaneously, increasing soil salinity prompted the earlier occurrence of the peak straw mineralization and PE. The contribution of straw mineralization to CO2 emissions on the 1st day significantly decreased with rising salinity levels (p < 0.05), while the opposite change was observed from 5 days to 120 days. Although PE significantly decreased with increasing salinity, the duration of the effect of straw input on soil organic matter mineralization increased substantially in high-salinity soils. These findings reveal the influence of soil salinity levels on the straw mineralization process and CO2 emission, which will help us assess and boost carbon sequestration in saline soils under straw input conditions.
期刊介绍:
Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.