Quantifying anthropogenic carbon inventory changes in the Pacific sector of the Southern Ocean

被引:39
作者
Williams, Nancy L. [1 ,2 ]
Feely, Richard A. [2 ]
Sabine, Christopher L. [2 ]
Dickson, Andrew G. [3 ]
Swift, James H. [3 ]
Talley, Lynne D. [3 ]
Russell, Joellen L. [4 ]
机构
[1] Univ Washington, Sch Oceanog, Seattle, WA 98195 USA
[2] NOAA, Pacific Marine Environm Lab, Seattle, WA 98115 USA
[3] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[4] Univ Arizona, Dept Geosci, Tucson, AZ 85721 USA
基金
美国国家科学基金会; 美国海洋和大气管理局;
关键词
Carbon dioxide; Dissolved inorganic carbon; Anthropogenic carbon; pH; Carbonate chemistry; Ocean acidification; Apparent oxygen utilization; Hydrography; Southern ocean; Decadal change; DISSOLVED INORGANIC CARBON; ANTARCTIC INTERMEDIATE WATER; TIME-SERIES; INDIAN-OCEAN; CO2; UPTAKE; DIOXIDE ANALYSIS; TEMPORAL-CHANGES; SURFACE OCEAN; ACIDIFICATION; STORAGE;
D O I
10.1016/j.marchem.2015.06.015
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Southern Ocean plays a major role in mediating the uptake, transport, and long-term storage of anthropogenic carbon dioxide (CO2) into the deep ocean. Examining the magnitude and spatial distribution of this oceanic carbon uptake is critical to understanding how the earth's carbon system will react to continued increases in this greenhouse gas. Here, we use the extended multiple linear regression technique to quantify the total and anthropogenic change in dissolved inorganic carbon (DIC) along the S04P and P16S CLIVAR/U.S. Global Ocean Carbon and Repeat Hydrography Program lines south of 67 degrees S in the Pacific sector of the Southern Ocean between 1992 and 2011 using discrete bottle measurements from repeat occupations. Along the S04P section, which is located in the seasonal sea ice zone south of the Antarctic Circumpolar Current in the Pacific, the anthropogenic component of the DIC increase from 1992 to 2011 is mostly found in the Antarctic Surface Water (AASW, upper 100 m), while the increase in DIC below the mixed layer in the Circumpolar Deep Water can be primarily attributed to either a slowdown in circulation or decreased ventilation of deeper, high CO2 waters. In the AASW we calculate an anthropogenic increase in DIC of 12-18 mu mol kg(-1) and an average storage rate of anthropogenic CO2 of 0.10 +/- 0.02 mol m(-2) yr(-1) for this region compared to a global average of 0.5 +/- 0.2 mol m(-2) yr(-1). In surface waters this anthropogenic CO2 uptake results in an average pH decrease of 0.0022 +/- 0.0004 pH units yr(-1), a 0.47 +/- 0.10% yr(-1) decrease in the saturation state of aragonite (Omega(Aragonite)) and a 2.0 +/- 0.7 m yr(-1) shoaling of the aragonite saturation horizons (calculated for the Omega(Aragonite) = 1.3 contour). (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:147 / 160
页数:14
相关论文
共 121 条
  • [1] Anderson L.A., 1994, GLOB BIOGEOCHEM CYCL
  • [2] [Anonymous], 2005, ORNLCDIAC145
  • [3] [Anonymous], CARBON DIOXIDE HYDRO
  • [4] [Anonymous], 2011, MATLAB PROGRAM DEV C, DOI DOI 10.3334/CDIAC/OTG.CO2SYS_MATLAB_V1.1
  • [5] [Anonymous], 1994, HDB METHODS ANAL VAR
  • [6] [Anonymous], 2013, Climate Change 2013: The physical science basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change
  • [7] [Anonymous], ORNLCDIAC155 US DEP
  • [8] [Anonymous], 1998, ORNL CDIAC
  • [9] A Time-Series View of Changing Surface Ocean Chemistry Due to Ocean Uptake of Anthropogenic CO2 and Ocean Acidification
    Bates, Nicholas R.
    Astor, Yrene M.
    Church, Matthew J.
    Currie, Kim
    Dore, John E.
    Gonzalez-Davila, Melchor
    Lorenzoni, Laura
    Muller-Karger, Frank
    Olafsson, Jon
    Magdalena Santana-Casiano, J.
    [J]. OCEANOGRAPHY, 2014, 27 (01) : 126 - 141
  • [10] Beaupre M.-C., 2005, CRUISE REPORT WOCE S