Abstract

Abstract. The effect of ocean acidification and changing water conditions on primary (and secondary) marine aerosol emissions is not well understood on a regional or a global scale. To investigate this effect as well as the indirect effect on aerosol that changing biogeochemical parameters can have, ~ 52 m3 pelagic mesocosms were deployed for several weeks in the Mediterranean Sea during both winter pre-bloom and summer oligotrophic conditions and were subjected to various levels of CO2 to simulate the conditions foreseen in this region for the coming decades. After seawater sampling, primary bubble-bursting aerosol experiments were performed using a plunging water jet system to test both chemical and physical aerosol parameters (10–400 nm). Comparing results obtained during pre-bloom and oligotrophic conditions, we find the same four log-normal modal diameters (18.5 ± 0.6, 37.5 ± 1.4, 91.5 ± 2.0, 260 ± 3.2 nm) describing the aerosol size distribution during both campaigns, yet pre-bloom conditions significantly increased the number fraction of the second (Aitken) mode, with an amplitude correlated to virus-like particles, heterotrophic prokaryotes, TEPs (transparent exopolymeric particles), chlorophyll a and other pigments. Organic fractions determined from kappa closure calculations for the diameter, Dp ~ 50 nm, were much larger during the pre-bloom period (64 %) than during the oligotrophic period (38 %), and the organic fraction decreased as the particle size increased. Combining data from both campaigns together, strong positive correlations were found between the organic fraction of the aerosol and chlorophyll a concentrations, heterotrophic and autotrophic bacteria abundance, and dissolved organic carbon (DOC) concentrations. As a consequence of the changes in the organic fraction and the size distributions between pre-bloom and oligotrophic periods, we find that the ratio of cloud condensation nuclei (CCN) to condensation nuclei (CN) slightly decreased during the pre-bloom period. The enrichment of the seawater samples with microlayer samples did not have any effect on the size distribution, organic content or the CCN activity of the generated primary aerosol. Partial pressure of CO2, pCO2, perturbations had little effect on the physical or chemical parameters of the aerosol emissions, with larger effects observed due to the differences between a pre-bloom and oligotrophic environment.

Highlights

  • With oceans covering 71 % of the Earth’s surface, sea spray aerosol comprises a large portion of the natural aerosol emissions, with an estimated contribution between 2000 and 10 000 Tg yr−1 for aerosols with diameter Dp < 20 μm (Gantt and Meskhidze, 2013)

  • Comparing results obtained during pre-bloom and oligotrophic conditions, we find the same four lognormal modal diameters (18.5± 0.6, 37.5± 1.4, 91.5± 2.0, 260± 3.2 nm) describing the aerosol size distribution during both campaigns, yet pre-bloom conditions significantly increased the number fraction of the second (Aitken) mode, with an amplitude correlated to virus-like particles, heterotrophic prokaryotes, Transparent exopolymeric particle (TEP), chlorophyll a and other pigments

  • While several studies have shown the effects of ocean acidification on biogeochemical parameters in eutrophic waters (Galgani et al, 2014; Schulz et al, 2013), observations from the MedSea experiment showed no effect of ocean acidification on most of the biogeochemical parameters in these oligo- to mesotrophic areas

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Summary

Introduction

With oceans covering 71 % of the Earth’s surface, sea spray aerosol comprises a large portion of the natural aerosol emissions, with an estimated contribution between 2000 and 10 000 Tg yr−1 for aerosols with diameter Dp < 20 μm (Gantt and Meskhidze, 2013). Marine aerosol can be produced from primary processes (e.g. sea spray aerosol from breaking waves) and secondary processes (i.e. formation via chemical processing or gas-to-particle conversion). These aerosols can have a large impact upon the Earth’s radiative budget through both direct effects, such as light scattering, and indirect effects, by becoming cloud condensation nuclei (CCN) and affecting cloud formation and cloud properties (Novakov and Corrigan, 1996; Novakov and Penner, 1993). The sea surface microlayer has been shown to exhibit physical, chemical and biological differences from oceanic subsurface water (Cunliffe et al, 2013)

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