Polycyclic aromatic hydrocarbons (PAHs) are excellent tracers for fossil fuel combustion, natural fires and petroleum contamination, and have been widely used for reconstructing past wildfires and industrial activities at a variety of time scales. Here, for the first time, we obtain a high resolution (annual to decadal scale) record of PAHs from two parallel marine sediment cores from the Liaodong Bay, Northeastern China to reconstruct the industrial activities, spanning the past ∼ 200 years from 1815 to 2014. Our data indicate that PAH variations can be divided into four episodes: I) low (probably near background) PAHs from natural fires and domestic wood combustion during the pre-industrial period from 1815 to 1890; II) slightly increased (but with large fluctuations) PAH concentrations derived from intermittent warfare during the World War (1891-1945) and increased industrial activities after 1946 (1946-1965); III) a period of stagnation and, in some cases, reduction in PAHs during the \"Cultural Revolution\" (1966 to 1979); and IV) a rapid and persistent rise in PAHs post 1979 linked to fast economic development, with PAH concentrations doubled from 1979 to 2014. Changes in PAH distributions demonstrate major shifts in the dominant types of fuels over time from vegetation/wood, to coal and wood, followed by coal and petroleum (including vehicle emissions) over the past 200 years. We find that PAH records also show similar trend to domestic economy and the estimated regional Anthropocene CO2 emissions from industrial activities, suggesting sedimentary PAH fluxes could be used as an indirect and qualitative proxy to track the trend for regional anthropogenic CO2 emissions.

An evaluation of the history of anthropogenic mercury (Hg) emissions is needed to quantify total atmospheric Hg emissions since the Industrial Revolution. Thus more long-term records of Hg accumulation rate from natural archives are needed. In the present study, a sediment core from Tianchi Lake, a crater lake in northeastern China, was used to reconstruct atmospheric Hg accumulation rates during the past 800 years. The results show that both Hg concentration and Hg accumulation rate began to increase from 29.5 to 40.2 ng g-1 and from 1.44 to 2.26 μg m-2 yr-1, respectively, at ~ 1750 AD, synchronous with the initiation of the Industrial Revolution. The Hg accumulation rate and Hg concentration increased significantly at ~ 1850 AD, and subsequently, there were two prominent peaks, at ~ 1940 AD and ~ 1980 AD, which are temporally consistent with the Second World War and the peak in commercial usage of Hg, respectively. The Hg accumulation rate and Hg concentration decreased after ~ 1980 AD, possibly because of the decrease in the global Hg background at that time. Differences in regional Hg emissions and atmospheric circulation may be responsible for the different trends in Hg accumulation rate after ~ 1980 AD in the Tibetan Plateau and northeastern China. Our results provide new data for evaluating natural and anthropogenic Hg emissions to the atmosphere in China.