Abstract

Abstract. Increasing atmospheric CO2 is decreasing ocean pH most rapidly in colder regions such as the Arctic. As a component of the EPOCA (European Project on Ocean Acidification) pelagic mesocosm experiment off Spitzbergen in 2010, we examined the consequences of decreased pH and increased pCO2 on the concentrations of dimethylsulphide (DMS). DMS is an important reactant and contributor to aerosol formation and growth in the Arctic troposphere. In the nine mesocosms with initial pHT 8.3 to 7.5, equivalent to pCO2 of 180 to 1420 μatm, highly significant but inverse responses to acidity (hydrogen ion concentration [H+]) occurred following nutrient addition. Compared to ambient [H+], average concentrations of DMS during the mid-phase of the 30 d experiment, when the influence of altered acidity was unambiguous, were reduced by approximately 60% at the highest [H+] and by 35% at [H+] equivalent to 750 μatm pCO2, as projected for 2100. In contrast, concentrations of dimethylsulphoniopropionate (DMSP), the precursor of DMS, were elevated by approximately 50% at the highest [H+] and by 30% at [H+] corresponding to 750 μatm pCO2. Measurements of the specific rate of synthesis of DMSP by phytoplankton indicate increased production at high [H+], in parallel to rates of inorganic carbon fixation. The elevated DMSP production at high [H+] was largely a consequence of increased dinoflagellate biomass and in particular, the increased abundance of the species Heterocapsa rotundata. We discuss both phytoplankton and bacterial processes that may explain the reduced ratios of DMS:DMSPt (total dimethylsulphoniopropionate) at higher [H+]. The experimental design of eight treatment levels provides comparatively robust empirical relationships of DMS and DMSP concentration, DMSP production and dinoflagellate biomass versus [H+] in Arctic waters.

Highlights

  • The surface energy budget of the Arctic is heavily influenced by cloud formation proSceossleisd(CEuarryrteht al., 1996; Sedlar et al, 2011), which correspondingly play an important role in the melting and freezing of the perennial sea ice (Kay and Gettelman, 2009)

  • In addition to monitoring how DMS and DMSP concentrations vary, we addressed two key factors that potentially alter DMS concentrations at different levels of acidity: (i) direct measures of DMSP synthesis rates by phytoplankton; and (ii) determination of which components of the phytoplankton communities contribute to the variations in DMSP production

  • During PII of the European Project on Ocean Acidification (EPOCA) mesocosm experiment, variations in composition and/or physiology of natural Arctic microbial communities resulted in daily average concentrations of DMS that were 35 (±11) % lower at [H+] concentrations that are projected to occur in 2100, compared to present conditions

Read more

Summary

Introduction

The surface energy budget of the Arctic is heavily influenced by cloud formation proSceossleisd(CEuarryrteht al., 1996; Sedlar et al, 2011), which correspondingly play an important role in the melting and freezing of the perennial sea ice (Kay and Gettelman, 2009). The dominance in summer of small Aitken-mode aerosol particles has been correlated to cspohnecreinctrDatMioSns(doifmMethSTyAlhsu(emlpehCtihdraeyn),eosssuugplgfohensetiicnrgeacaidli)naknbdetawtmeeonthe magnitude of DMS emission and cloud albedo over the Arctic (Ferek et al, 1995; Quinn et al, 2002). Archer et al.: Contrasting responses of DMS and DMSP to ocean acidification in Arctic waters unless proposed mechanisms of particle fragmentation are substantiated (Karl et al, 2012). Further evidence of the potential importance of DMS to Arctic albedo is provided by a chemical transport model with size-resolved aerosol microphysics, which illustrates the substantial contribution of sulphuric acid to formation of CCN (cloud condensation nuclei) during the Arctic summer (Korhonen et al, 2008). Understanding how DMS emissions are likely to alter in the future is especially important in relation to the rapidly changing Arctic climate

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

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