Atmospheric chemistry

Marine sulfur cycle

Separating biological change from pollution-driven shifts in atmospheric oxidation and methanesulfonic acid (MSA).

Satellite view of a phytoplankton bloom in the Gulf of Alaska
NASA • Phytoplankton bloom in Gulf of Alaska

Marine phytoplankton release dimethyl sulfide (DMS), a gas that helps form atmospheric aerosols and influences cloud formation over the oceans. One of its oxidation products, methanesulfonic acid (MSA), is preserved in polar ice cores and has long been used as a proxy for past marine productivity. However, many Arctic ice-core records show a sharp decline in MSA beginning during the Industrial Era—a trend that was widely interpreted as evidence of crashing phytoplankton populations.

Using ice cores from Denali and Greenland together with atmospheric chemistry modeling, we found a different explanation. Rather than reflecting widespread changes in ocean biology, the decline in MSA is primarily the result of anthropogenic air pollution altering the chemistry of the atmosphere. As illustrated in Figure 1, pollution changes the oxidation pathways of DMS, causing less MSA to form before the air masses reach the Arctic. This work demonstrates that industrial emissions have fundamentally altered atmospheric chemistry even in Earth's most remote regions, while also redefining how scientists interpret one of the Arctic's most important ice-core proxies for the marine environment.

Related publications

Schematic showing how pollution alters dimethyl sulfide oxidation and reduces methanesulfonic acid deposition in Arctic ice
Figure 1. Human-caused air pollution has altered the atmospheric chemistry of marine sulfur. By changing the oxidation pathways of dimethyl sulfide (DMS), pollution causes a greater fraction of DMS to be converted into sulfate (SO₄²⁻) and a smaller fraction into methanesulfonic acid (MSA), reducing the amount of MSA preserved in Arctic ice cores.