Global warming amplified by reduced sulphur fluxes as a result of ocean acidification

被引:6
|
作者
Six, Katharina D. [1 ]
Kloster, Silvia [1 ]
Ilyina, Tatiana [1 ]
Archer, Stephen D. [2 ,3 ]
Zhang, Kai [4 ]
Maier-Reimer, Ernst [1 ]
机构
[1] Max Planck Inst Meteorol, D-20146 Hamburg, Germany
[2] Plymouth Marine Lab, Plymouth PL1 3DH, Devon, England
[3] Bigelow Lab Ocean Sci, East Boothbay, ME 04544 USA
[4] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
DMS CYCLE; CLIMATE; CO2; SENSITIVITY; ATMOSPHERE;
D O I
10.1038/NCLIMATE1981
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Climate change and decreasing seawater pH (ocean acidification)(1) have widely been considered as uncoupled consequences of the anthropogenic CO2 perturbation(2,3). Recently, experiments in seawater enclosures (mesocosms) showed that concentrations of dimethylsulphide (DMS), a biogenic sulphur compound, were markedly lower in a low-pH (e)nvironment4. Marine DMS emissions are the largest natural source of atmospheric sulphur(5) and changes in their strength have the potential to alter the Earth's radiation budget(6). Here we establish observational-based relationships between pH changes and DMS concentrations to estimate changes in future DMS emissions with Earth system model(7) climate simulations. Global DMS emissions decrease by about 18(+/-3)% in 2100 compared with pre-industrial times as a result of the combined effects of ocean acidification and climate change. The reduced DMS emissions induce a significant additional radiative forcing, of which 83% is attributed to the impact of ocean acidification, tantamount to an equilibrium temperature response between 0.23 and 0.48 K. Our results indicate that ocean acidification has the potential to exacerbate anthropogenic warming through a mechanism that is not considered at present in projections of future climate change.
引用
收藏
页码:975 / 978
页数:4
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