首页|赣南稀土尾矿山土体硝态氮累积特征研究

赣南稀土尾矿山土体硝态氮累积特征研究

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稀土开采会造成大量浸矿剂(硫酸铵)残留在土壤中,高浓度铵态氮(NH4+-N)可能在生物化学作用下转化为硝态氮(NO3--N)。为探明NO3--N在稀土尾矿山土体内的含量及影响因素,明确硝酸盐污染程度,本研究选择赣南地区一个离子型稀土原地浸矿尾矿山,由表土分层采样至基岩面,并分析土壤NO3--N及相关的理化性质。研究结果表明,尾矿山土体NO3--N含量变异范围非常大(2。80~193。99 mg·kg-1),其平均值为46。30±55。16 mg·kg-1,表层土壤NO3--N含量范围为2。89~6。75 mg·kg-1,与自然土壤相近;表层以下土壤NO3--N含量明显高于自然土壤。尾矿山土体深部含矿层土壤NO3--N含量明显高于表层,NO3--N 含量随深度的分布规律与自然土壤相反,这是矿体部分残留大量浸矿剂造成的。土壤NH4+-N 含量主导了NO3--N的产生量,但NO3--N在土体不同深度、山体不同部位的累积量还受降雨淋溶及NO3--N迁移过程的控制。开采结束4年后,尾矿山内累积的NO3--N仍不断向环境中释放。长期来看,尾矿山土壤中富集的NH4+-N将不断转化为NO3--N并随水迁移,持续威胁生态环境及人类健康。本研究可为稀土原地浸矿场地土壤及下游水体污染的评价和治理提供理论基础与科学支撑。
Study on the Characteristics of Soil Nitrate Nitrogen Accumulation of Rare Earth Tailing in Southern Jiangxi
[Objective]Rare earth mining excessively increased the content of leaching agents(e.g.ammonium sulfate)in the soil.The high concentration of ammonium nitrogen(NH4+-N)may be converted into nitrate nitrogen(NO3--N)under active biochemical action,resulting in potential environmental risks,especially nitrate pollution of water bodies around tailings.Therefore,it is necessary to evaluate the content of soil NO 3--N,explore the influencing factors and understand the nitrate pollution degree of the rare earth tailings.[Method]We chose an ionic rare earth tailing after in-situ mining in southern Jiangxi province,which used ammonium sulfate as a leaching agent.Up to sampling,this mine had been closed for 4 years.We set three sampling points regularly from the top to bottom of this mine and collected soil profile samples in different layers from the topsoil to the bedrock.Soil samples were divided into two parts.One part was stored at a low temperature to analyze soil nitrate nitrogen and ammonium nitrogen.The other one was used for analyzing relevant physical and chemical properties after air drying.[Result]The results showed that the variation range of soil NO 3--N content in the tailing area was large(2.80 to 193.99 mg·kg-1),with a mean of 46.30±55.16 mg·kg-1.The content of topsoil NO 3--N was 2.89-6.75 mg·kg-1,which was similar to that of natural soil.Also,the content of NO3--N in the soil below surface layer was significantly higher than that in the natural soil.The soil NO 3--N of the ore-bearing layer in the deep profile was higher than that of the top layer.Moreover,the distribution of NO 3--N with depth was different from that of the natural soil and was mainly caused by a large number of leaching agents remaining in the ore body.NH 4+-N content dominated the generation of NO 3--N and determined the upper limit of soil NO 3--N accumulation.The accumulation degree of NO 3--N in different soil layers and different parts of mountains was controlled by rainfall leaching and the NO 3--N migration process.However,the soil's physical and chemical properties,including water content,cation exchange capacity and particle composition,had no significant correlation with NO 3--N content,and were not the determining factors of NO 3--N content.[Conclusion]The soil NO 3--N in the tailing mainly originated from nitrification.Four years after mining,a large amount of NH 4+-N remained in the tailing,and the NO 3--N generated by nitrification was continuously released into the environment.In the long term,the soil NH 4+-N enriched in tailing will be transformed into NO 3--N and the NO 3--N will migrate with water,threatening the ecological environment and human health.This study can provide a theoretical basis and scientific reference for the assessment and treatment of soil and downstream water pollution in rare earth in-situ leaching sites.

Nitrogen transformationNitrate nitrogen distributionNitrate nitrogen migrationIonic rare earthMine soil

许哲、杨金玲、赵越、张甘霖

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土壤与农业可持续发展国家重点实验室(中国科学院南京土壤研究所),南京 210008

中国科学院大学,北京 100049

中国科学院南京地理与湖泊研究所,南京 210008

氮转化 硝态氮分布 硝态氮迁移 离子型稀土 矿区土壤

国家重点研发计划

2018YFC1801801

2024

土壤学报
中国土壤学会

土壤学报

CSTPCD北大核心
影响因子:2
ISSN:0564-3929
年,卷(期):2024.61(3)
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