Abstract
Abstract. Chemical and aerosol processes in the transition from closed- to open-cell circulation in the remote, cloudy marine boundary layer are explored. It has previously been shown that precipitation can initiate a transition from the closed- to the open-cellular state, but that the boundary layer cannot maintain this open-cell state without a resupply of cloud condensation nuclei (CCN). Potential sources of CCN include wind-driven production of sea salt from the ocean, nucleation from the gas phase, and entrainment from the free troposphere. In order to investigate CCN sources in the marine boundary layer and their role in supplying new particles, we have coupled in detail chemical, aerosol, and cloud processes in the WRF/Chem model, and added state-of-the-art representations of sea salt emissions and aerosol nucleation. We conduct numerical simulations of the marine boundary layer in the transition from a closed- to an open-cell state. Results are compared with observations in the Southeast Pacific boundary layer during the VAMOS Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx). The transition from the closed- to the open-cell state generates conditions that are conducive to nucleation by forming a cloud-scavenged, ultra-clean layer below the inversion base. Open cell updrafts loft dimethyl sulfide from the ocean surface into the ultra-clean layer, where it is oxidized during daytime to SO2 and subsequently to H2SO4. Low H2SO4 condensation sink values in the ultra-clean layer allow H2SO4 to rise to concentrations at which aerosol nucleation produces new aerosol in significant numbers. The existence of the ultra-clean layer is confirmed by observations. We find that the observed DMS flux from the ocean in the VOCALS-REx region can support a nucleation source of aerosol in open cells that exceeds sea salt emissions in terms of the number of particles produced. The freshly nucleated, nanometer-sized aerosol particles need, however, time to grow to sizes large enough to act as CCN. In contrast, mechanical production of particles from the ocean surface by near-surface winds provides a steady source of larger particles that are effective CCN at a rate exceeding a threshold for maintenance of open-cell circulation. Entrainment of aerosol from the free troposphere contributes significantly to boundary layer aerosol for the considered VOCALS-REx case, but less than sea salt aerosol emissions.
Highlights
We find that the observed dimethyl sulfide (DMS) flux from the ocean in the VOCALS-REx region can support a nucleation source of aerosol in open cells that exceeds sea salt emissions in terms of the number of particles produced
To study the role of aerosol sources in supplying new particles in this complex, interactive system, we have coupled in detail chemical, aerosol, and cloud processes in the WRF/Chem model (Grell et al, 2005), and added representations of primary oceanic emissions (Clarke et al, 2006) and of aerosol nucleation from the gas phase (Kazil et al, 2010)
Trajectory calculations and satellite imagery indicate that the marine boundary layer (MBL) sampled in VOCALS-REx RF06 experienced a transition from closed- to open-cell circulation approximately in the 12 h preceding the RF06 measurements (Wood et al, 2010)
Summary
The cloudy marine boundary layer (MBL) is of much interest from a climate system perspective. Open-cell regions are potential candidates for the CLAW hypothesis (Charlson et al, 1987), which proposes that in broken cloud situations ocean phytoplankton respond to the increased surface (solar) radiation and temperature by producing more DMS, which in turn, results in stronger aerosol nucleation in the MBL, an increased number of aerosol particles, and a higher cloud albedo/fraction. To study the role of aerosol sources in supplying new particles in this complex, interactive system, we have coupled in detail chemical, aerosol, and cloud processes in the WRF/Chem model (Grell et al, 2005), and added representations of primary oceanic emissions (Clarke et al, 2006) and of aerosol nucleation from the gas phase (Kazil et al, 2010). Further details on the coupling between chemical, aerosol, and cloud processes used in this work are given in Appendix A
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