News

New study from Hokkaido University details processes that keep pollutants aloft despite a drop in emissions.

The ice core used in the study (Photo: Mai Matsumoto)

Nitrates in the atmosphere reduce air quality and play an important role in climate change. An international team led by Hokkaido University researchers has revealed how chemical processes in the atmosphere have led to persistently high nitrate levels despite a reduction in emissions over the past few decades. These findings, published in Nature Communications, will help improve climate modelling by refining our ability to assess and predict atmospheric nitrate levels.

Atmospheric nitrate levels peaked between 1970 and 2000. The levels decreased somewhat with the decrease in the emission of nitrate precursors since the 1990s, but the drop in nitrate levels is smaller than the drop in the emission of precursors—something is keeping nitrates in the atmosphere.

Nitrates can exist in either a gaseous or particulate form in the atmosphere. Gaseous nitrate is more easily deposited out of the atmosphere, while the particulate form—particularly finer particles—can be transported over long distances. Understanding the balance between gaseous and particulate nitrates is therefore important in getting a picture of the atmospheric dynamics and persistence of nitrates.

The persistence of atmospheric nitrates in source regions is explained by a buffering effect, where gaseous nitrates are converted to particulate nitrates, contributing to their persistence. The impact of this buffering over long timescales and at long ranges is unclear, but nitrates deposited in Arctic ice cores show the same patterns as atmospheric nitrates. These sites are far from the sources, so the continuing high deposition rates don’t reflect local processes near the source but must be due to atmospheric transport and other processes in the atmosphere.

To understand these dynamics, a research team led by Professor Yoshinori Iizuka at the Institute of Low Temperature Science, Hokkaido University, examined the nitrate deposition history from 1800 to 2020 in an ice core taken from southeastern Greenland. As expected, nitrate levels within the core increased from the 1850s, peaking between the 1970s and 2000s before declining somewhat but remaining high. Overall, the increase in nitrates up to the 1970s happened more gradually than the increase in precursors, and the decrease after the 1990s was also slower and smaller than the decrease in precursor emission.

Since the 1990s, although nitrate emissions have decreased greatly (graph, orange line), the Greenland SE-Dome ice core shows that particulate nitrates have persisted (graph, black line). This is due to a buffering effect where gaseous nitrates are converted to particulate nitrates even though emissions have decreased; these particulate nitrates were transported to the Arctic and recorded in the Arctic ice. (Illustration: Sakiko Ishino)

The delayed effect and persistence of nitrates indicates factors other than the emission of precursors are affecting nitrate levels. The researchers investigated these factors with a global chemical transport model and found that the difference between nitrate and precursor levels correlated with atmospheric acidity and not with other meteorological factors, such as air temperature.

In other words, the persistence of nitrates has been driven by chemical processes happening in the atmosphere rather than meteorological conditions or atmospheric dynamics. Changes in atmospheric acidity altered the proportion of nitrate that was gaseous or particulate. This affects the lifetime of nitrates in the atmosphere. Atmospheric acidity has increased the fraction of nitrates in particulate form, enabling this pollutant to persist longer and travel farther.

“Ours is the first study to present accurate information for records of particulate nitrates in ice cores, which has been a very challenging problem,” says Iizuka. “As it is more difficult to reduce anthropogenic emissions of substances that lead to increased nitrates, accurate measurements of particulate nitrates in the ice cores provides data for increasing the accuracy of predicting the amplification of Arctic warming in the future.”

“It was difficult to present accurate nitrate from ice cores, but our team was able to do so this time.” says Iizuka. “In the future, nitrate will replace sulfate as the primary aerosol in the Arctic, suggesting this result leads to the higher accuracy of future predictions of Arctic warming amplification.”

Sumito Matoba (left) and Yoshinori Iizuka (right) drilling the ice core in Greenland. (Photo: Tetsuhide Yamasaki)

Original article:

Yoshinori Iizuka, et al. Acidity-driven gas-particle partitioning of nitrate regulates its transport to Arctic through the industrial era. Nature Communications. May 19, 2025.
DOI: 10.1038/s41467-025-59208-0

Funding:

This study was supported by Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)/Japan Society for the Promotion of Science (JSPS) KAKENHI (23H00511, 23K18516, 18H05292, 26257201, 23H03522, 20H04305, JP23K18519, JP23K24976); the Arctic Challenge for Sustainability (ArCS II) Project (JPMXD1420318865); the National Science Foundation of China (W2441015, 42494851, 42494852, 42473011); the Fundamental Research Funds for the Central Universities (0206/14380918, 0206/143802024, 0206/14380150, 0206/14380185, 0206/14380174), International Collaboration Program (2024300346, 0206/14380918); Cemac “GeoX” Inter-disciplinary Program (Grant no. 2024300245); startup funding from Nanjing University; the Institute of Nature and Environmental Technology, Kanazawa University (24006); and the Environment Research and Technology Development Fund 2-2301 (JPMEERF20232001) of the Environmental Restoration and Conservation Agency of Japan (ERCA).

Contacts:

Professor Yoshinori Iizuka
Institute of Low Temperature Science
Hokkaido University
Tel: +81-11-706-7351
Email: iizuka[at]lowtem.hokudai.ac.jp

Naoki Namba
Public Relations & Communications Division
Office of Public Relations and Social Collaboration
Hokkaido University
Tel: +81-11-706-2185
Email: en-press[at]general.hokudai.ac.jp