Abstract

As an important component of carbonaceous particles, organic carbon (OC) plays a significant role in radiative forcing in the atmosphere. Recently, the warming effect of light-absorbing OC has been emphasized. Water-soluble organic carbon (WSOC) is commonly used as a surrogate to investigate the light absorption of OC. Thus far, filters with 0.45 μm (PS1) and 0.20 μm pore sizes (PS2) are both used to investigate the light absorption of WSOC, which may cause large divergent results. In this study, we found that the light absorption ability of WSOC treated with PS1 was higher than that of PS2 due to the extinction of suspended particles (e.g., black carbon) with particle size between 0.20 μm and 0.45 μm, although the concentrations of WSOC treated with PS1 and PS2 were very close. This phenomenon was more remarkable at visible wavelengths, resulting in an overestimation of the warming effect of WSOC by 9%–22% for aerosol samples treated by PS1, with the highest values occurring in samples heavily influenced by fossil fuel burning emissions. An overestimation of WSOC light absorption treated by PS1 occurred in the investigated ambient aerosol samples from three sites, so it may be a general phenomenon that also exists in other regions of the world. Therefore, to achieve the actual solar radiative forcing of OC in the atmosphere, it is recommended to use PS2 in the future, and reported data of WSOC treated by PS1 should be re-evaluated.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.