Anthropogenic-Driven Alterations in Black Carbon Sequestration and the Structure in a Deep Plateau Lake

被引:28
作者
Huang, Changchun [1 ,2 ,3 ,6 ]
Lu, Lingfeng [1 ,2 ]
Li, Yi [1 ,2 ]
He, Yao [1 ,2 ]
Shang, Nana [1 ,2 ]
Bai, Yixin [1 ,2 ]
Yu, Heyu [1 ,2 ]
Huang, Tao [1 ,2 ]
Zhu, A-Xing [1 ,3 ,4 ]
Yang, Hao [1 ,2 ]
Zhao, Kan [1 ,2 ]
Yu, Yanhong [5 ]
机构
[1] Nanjing Normal Univ, Jiangsu Ctr Collaborat Innovat Geog Informat Reso, Nanjing 210023, Peoples R China
[2] Nanjing Normal Univ, Sch Geog Sci, Nanjing 210023, Peoples R China
[3] Nanjing Normal Univ, Key Lab Virtual Geog Environm, Minist Educ, Nanjing 210023, Peoples R China
[4] Univ Wisconsin, Dept Geog, Madison, WI 53706 USA
[5] Yunnan Res Acad Ecoenvironm Sci, Kunming 650034, Yunnan, Peoples R China
[6] Chinese Acad Sci, Nanjing Inst Geog & Limnol, State Key Lab Lake Sci & Environm, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; ORGANIC-CARBON; SOURCE APPORTIONMENT; ELEMENTAL CARBON; PYROGENIC CARBON; TIBETAN PLATEAU; NITROGEN BURIAL; RISK-ASSESSMENT; SEDIMENTS; EMISSIONS;
D O I
10.1021/acs.est.1c00106
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The continuous flux of organic carbon (OC) from terrestrial ecosystems into inland water is an important component of the global carbon cycle. The buried OC pool in inland water sediments is considerable, and black carbon (BC) is a significant contributor to this OC pool because of the continuous growth in BC emissions. Therefore, determining the effect of BC on total OC burial and variations in the structure of BC during the burial process will contribute significantly to our understanding of lacustrine carbon cycling. This study investigated BC burial and its structural variations in response to anthropogenic drivers using four dated sedimentary cores from a deep plateau lake in China. The BC burial rate rose from 0.96 +/- 0.64 g.m(-2).y(-1) (mean of sedimentary cores pre-1960s) to 4.83 +/- 1.25 g.m(-2).y(-1) (after 2000), which is a 5.48 +/- 2.12-fold rise. The increase of char was similar to those of BC. The growth rate of soot was 7.20 +/- 4.30 times, which is higher than that of BC and char, increasing from 0.12 +/- 0.08 to 0.64 +/- 0.23 g.m(-2).y(-1). There was a decreasing trend in the ratio of char and soot at a mean rate of 62.8 +/- 6.46% (excluding core 3) in relation to increased fossil fuel consumption. The contribution of BC to OC burial showed a significant increasing trend from the past to the present, particularly in cores 3 and 4, and the mean contribution of the four cores was 11.78 +/- 2.84%. Source tracer results from positive matrix factorization confirmed that the substantial use of fossil fuels has promoted BC burial and altered the BC structure. This has resulted in BC with a higher aromatic content in the lake sediment, which exhibits reduced reactivity and increased stability. The strong correlation between BC and allochthonous total OC indicates that the input pathways of the buried BC in this plateau lake sediment were terrestrial surface processes and not atmospheric deposition.
引用
收藏
页码:6467 / 6475
页数:9
相关论文
共 78 条
  • [1] Land-use change, not climate, controls organic carbon burial in lakes
    Anderson, N. J.
    Dietz, R. D.
    Engstrom, D. R.
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2013, 280 (1769)
  • [2] [Anonymous], 1985, BLACK CARBON ENV
  • [3] Three decades of dating recent sediments by fallout radionuclides: a review
    Appleby, P. G.
    [J]. HOLOCENE, 2008, 18 (01) : 83 - 93
  • [4] Chemical (C, N, S, black carbon, soot and char) and stable carbon isotope composition of street dusts from a major West African metropolis: Implications for source apportionment and exposure
    Bandowe, Benjamin A. Musa
    Nkansah, Marian Asantewah
    Leimer, Sophia
    Fischer, Daniela
    Lammel, Gerhard
    Han, Yongming
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2019, 655 : 1468 - 1478
  • [5] Freshwater Methane Emissions Offset the Continental Carbon Sink
    Bastviken, David
    Tranvik, Lars J.
    Downing, John A.
    Crill, Patrick M.
    Enrich-Prast, Alex
    [J]. SCIENCE, 2011, 331 (6013) : 50 - 50
  • [6] The Pyrogenic Carbon Cycle
    Bird, Michael I.
    Wynn, Jonathan G.
    Saiz, Gustavo
    Wurster, Christopher M.
    McBeath, Anna
    [J]. ANNUAL REVIEW OF EARTH AND PLANETARY SCIENCES, VOL 43, 2015, 43 : 273 - 298
  • [7] Contrasting temporal trends and relationships of total organic carbon, black carbon, and polycyclic aromatic hydrocarbons in rural low-altitude and remote high-altitude lakes
    Bogdal, Christian
    Bucheli, Thomas D.
    Agarwal, Tripti
    Anselmetti, Flavio S.
    Blum, Franziska
    Hungerbuehler, Konrad
    Kohler, Martin
    Schmid, Peter
    Scheringer, Martin
    Sobek, Anna
    [J]. JOURNAL OF ENVIRONMENTAL MONITORING, 2011, 13 (05): : 1316 - 1326
  • [8] Bounding the role of black carbon in the climate system: A scientific assessment
    Bond, T. C.
    Doherty, S. J.
    Fahey, D. W.
    Forster, P. M.
    Berntsen, T.
    DeAngelo, B. J.
    Flanner, M. G.
    Ghan, S.
    Kaercher, B.
    Koch, D.
    Kinne, S.
    Kondo, Y.
    Quinn, P. K.
    Sarofim, M. C.
    Schultz, M. G.
    Schulz, M.
    Venkataraman, C.
    Zhang, H.
    Zhang, S.
    Bellouin, N.
    Guttikunda, S. K.
    Hopke, P. K.
    Jacobson, M. Z.
    Kaiser, J. W.
    Klimont, Z.
    Lohmann, U.
    Schwarz, J. P.
    Shindell, D.
    Storelvmo, T.
    Warren, S. G.
    Zender, C. S.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2013, 118 (11) : 5380 - 5552
  • [9] Characteristics and sources of carbonaceous aerosols from Shanghai, China
    Cao, J. -J.
    Zhu, C. -S.
    Tie, X. -X.
    Geng, F. -H.
    Xu, H. -M.
    Ho, S. S. H.
    Wang, G. -H.
    Han, Y. -M.
    Ho, K. -F.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2013, 13 (02) : 803 - 817
  • [10] Characterization and source apportionment of atmospheric organic and elemental carbon during fall and winter of 2003 in Xi'an, China
    Cao, JJ
    Wu, F
    Chow, JC
    Lee, SC
    Li, Y
    Chen, SW
    An, ZS
    Fung, KK
    Watson, JG
    Zhu, CS
    Liu, SX
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 : 3127 - 3137