7 research outputs found

    Quantifying changes in soil organic carbon density from 1982 to 2020 in Chinese grasslands using a random forest model

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    China has the second-largest grassland area in the world. Soil organic carbon storage (SOCS) in grasslands plays a critical role in maintaining carbon balance and mitigating climate change, both nationally and globally. Soil organic carbon density (SOCD) is an important indicator of SOCS. Exploring the spatiotemporal dynamics of SOCD enables policymakers to develop strategies to reduce carbon emissions, thus meeting the goals of “emission peak” in 2030 and “carbon neutrality” in 2060 proposed by the Chinese government. The objective of this study was to quantify the dynamics of SOCD (0–100 cm) in Chinese grasslands from 1982 to 2020 and identify the dominant drivers of SOCD change using a random forest model. The results showed that the mean SOCD in Chinese grasslands was 7.791 kg C m−2 in 1982 and 8.525 kg C m−2 in 2020, with a net increase of 0.734 kg C m−2 across China. The areas with increased SOCD were mainly distributed in the southern (0.411 kg C m−2), northwestern (1.439 kg C m−2), and Qinghai–Tibetan (0.915 kg C m−2) regions, while those with decreased SOCD were mainly found in the northern (0.172 kg C m−2) region. Temperature, normalized difference vegetation index, elevation, and wind speed were the dominant factors driving grassland SOCD change, explaining 73.23% of total variation in SOCD. During the study period, grassland SOCS increased in the northwestern region but decreased in the other three regions. Overall, SOCS of Chinese grasslands in 2020 was 22.623 Pg, with a net decrease of 1.158 Pg since 1982. Over the past few decades, the reduction in SOCS caused by grassland degradation may have contributed to soil organic carbon loss and created a negative impact on climate. The results highlight the urgency of strengthening soil carbon management in these grasslands and improving SOCS towards a positive climate impact

    Chemical profiles of urban fugitive dust over Xi'an in the south margin of the Loess Plateau, China

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    AbstractUrban fugitive dust samples were collected to determine the chemical profiles of fugitive dust over Xi'an. Seventy eight samples were collected and divided into categories of paved road dust, construction dust, cement dust, and soil dust. Eighteen elements, including Na, Mg, Al, Si, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Ba, and Pb, and eight water–soluble inorganic ions, including Na+, Mg2−, Ca2−, NH4−, F−, Cl−, NO3− and SO42−, were measured. The most abundant elements in these urban dust samples were Al, Si, Ca, and Fe. Al, Si, K, and Ti and showed strong positive correlations with each other, indicating they are typical dust trace elements. In contrast, elements of Ca, Zn, As, and Pb had negative correlations to crustal elements. Si/Al, K/Al, Ti/Al, Mn/Al, and Fe/Al ratios varied insignificantly among these four samples types; these ratios are similar to the properties of loess, desert, and Gobi soil dust reported in previous studies. A significantly higher Ca/Al ratio was dominant in the chemical profile of the cement samples. In addition, high Pb/Al and Zn/Al ratios were detected in comparison with those in the Gobi soil, desert soil, and loess soil samples, which indicated that Pb/Al and Zn/Al ratios can be considered as markers of urban dust. To t a l water–soluble ions occupied only a small fraction (<5%) in the urban fugitive soil samples indicating that most of the materials in the fugitive dust were insoluble. Ca2+ and SO42− were the most abundant ions in all samples. Most of the Ca and K in the fugitive soil samples were in insoluble phases, which differ significantly in comparison with combustion sources. A strong correlation was observed between Ca2+ and estimated CO32− levels indicating that most of Ca2+ was in the form of CaCO3 rather than other calcium minerals in Xi’an fugitive dust

    Chemical profiles of urban fugitive dust over Xi'an in the south margin of the Loess Plateau, China

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    Urban fugitive dust samples were collected to determine the chemical profiles of fugitive dust over Xi&#39;an. Seventy eight samples were collected and divided into categories of paved road dust, construction dust, cement dust, and soil dust. Eighteen elements, including Na, Mg, Al, Si, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Ba, and Pb, and eight water-soluble inorganic ions, including Na+, Mg2+, Ca2+, NH4+, F-, Cl-, NO3- and SO42-, were measured. The most abundant elements in these urban dust samples were Al, Si, Ca, and Fe. Al, Si, K, and Ti and showed strong positive correlations with each other, indicating they are typical dust trace elements. In contrast, elements of Ca, Zn, As, and Pb had negative correlations to crustal elements. Si/Al, K/Al, Ti/Al, Mn/Al, and Fe/Al ratios varied insignificantly among these four samples types; these ratios are similar to the properties of loess, desert, and Gobi soil dust reported in previous studies. A significantly higher Ca/Al ratio was dominant in the chemical profile of the cement samples. In addition, high Pb/Al and Zn/Al ratios were detected in comparison with those in the Gobi soil, desert soil, and loess soil samples, which indicated that Pb/Al and Zn/Al ratios can be considered as markers of urban dust. Total water-soluble ions occupied only a small fraction (&lt;5%) in the urban fugitive soil samples indicating that most of the materials in the fugitive dust were insoluble. Ca2+ and SO42- were the most abundant ions in all samples. Most of the Ca and K in the fugitive soil samples were in insoluble phases, which differ significantly in comparison with combustion sources. A strong correlation was observed between Ca2+ and estimated CO32- levels indicating that most of Ca2+ was in the form of CaCO3 rather than other calcium minerals in Xi&#39;an fugitive dust.</p
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