The Arctic is a sentinel of global change. This region is influenced by multiple physical and socio-economic drivers and feedbacks, impacting both the natural and human environment. Air pollution is one such driver that impacts Arctic climate change, ecosystems and health but significant uncertainties still surround quantification of these effects. Arctic air pollution includes harmful trace gases (e.g. tropospheric ozone) and particles (e.g. black carbon, sulphate) and toxic substances (e.g. polycyclic aromatic hydrocarbons) that can be transported to the Arctic from emission sources located far outside the region, or emitted within the Arctic from activities including shipping, power production, and other industrial activities. This paper qualitatively summarizes the complex science issues motivating the creation of a new international initiative, PACES (air Pollution in the Arctic: Climate, Environment and Societies). Approaches for coordinated, international and interdisciplinary research on this topic are described with the goal to improve predictive capability via new understanding about sources, processes, feedbacks and impacts of Arctic air pollution. Overarching research actions are outlined, in which we describe our recommendations for 1) the development of trans-disciplinary approaches combining social and economic research with investigation of the chemical and physical aspects of Arctic air pollution; 2) increasing the quality and quantity of observations in the Arctic using long-term monitoring and intensive field studies, both at the surface and throughout the troposphere; and 3) developing improved predictive capability across a range of spatial and temporal scales.

/pdf/arctic-air-pollution-challenges-and-opportunities-for-the-3fu5gfw7ot.pdf

Arctic air pollution: Challenges and opportunities for the next decade

Terrestrial vegetation releases large quantities of plant volatiles into the atmosphere that can then oxidize to form secondary organic aerosol. These particles affect plant productivity through the diffuse radiation fertilization effect by altering the balance between direct and diffuse radiation reaching the Earth’s surface. Here, using a suite of models describing relevant coupled components of the Earth system, we quantify the impacts of biogenic secondary organic aerosol on plant photosynthesis through this fertilization effect. We show that this leads to a net primary productivity enhancement of 1.23 Pg C yr−1 (range 0.76–1.61 Pg C yr−1 due to uncertainty in biogenic secondary organic aerosol formation). Notably, this productivity enhancement is twice the mass of biogenic volatile organic compound emissions (and ~30 times larger than the mass of carbon in biogenic secondary organic aerosol) causing it. Hence, our simulations indicate that there is a strong positive ecosystem feedback between biogenic volatile organic compound emissions and plant productivity through plant-canopy light-use efficiency. We estimate a gain of 1.07 in global biogenic volatile organic compound emissions resulting from this feedback.

/pdf/enhanced-global-primary-production-by-biogenic-aerosol-via-5dxsaz72sz.pdf

Enhanced global primary production by biogenic aerosol via diffuse radiation fertilization

During Biogenic Aerosols—Effects on Clouds and Climate (BAECC), the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) Program deployed the Second ARM Mobile Facility (AMF2) to Hyytiala, Finland, for an 8-month intensive measurement campaign from February to September 2014. The primary research goal is to understand the role of biogenic aerosols in cloud formation. Hyytiala is host to the Station for Measuring Ecosystem–Atmosphere Relations II (SMEAR II), one of the world’s most comprehensive surface in situ observation sites in a boreal forest environment. The station has been measuring atmospheric aerosols, biogenic emissions, and an extensive suite of parameters relevant to atmosphere–biosphere interactions continuously since 1996. Combining vertical profiles from AMF2 with surface-based in situ SMEAR II observations allows the processes at the surface to be directly related to processes occurring throughout the entire tropospheric column. Together with the inclusion of extensi...

https://opensky.ucar.edu:/islandora/object/articles%3A19369/datastream/PDF/view

BAECC: A Field Campaign to Elucidate the Impact of Biogenic Aerosols on Clouds and Climate

Secondary organic aerosol (SOA) accounts for a dominant fraction of the submicron atmospheric particle mass, but knowledge of the formation, composition and climate effects of SOA is incomplete and limits our understanding of overall aerosol effects in the atmosphere. Organic oligomers were discovered as dominant components in SOA over a decade ago in laboratory experiments and have since been proposed to play a dominant role in many aerosol processes. However, it remains unclear whether oligomers are relevant under ambient atmospheric conditions because they are often not clearly observed in field samples. Here we resolve this long-standing discrepancy by showing that elevated SOA mass is one of the key drivers of oligomer formation in the ambient atmosphere and laboratory experiments. We show for the first time that a specific organic compound class in aerosols, oligomers, is strongly correlated with cloud condensation nuclei (CCN) activities of SOA particles. These findings might have important implications for future climate scenarios where increased temperatures cause higher biogenic volatile organic compound (VOC) emissions, which in turn lead to higher SOA mass formation and significant changes in SOA composition. Such processes would need to be considered in climate models for a realistic representation of future aerosol-climate-biosphere feedbacks.

https://biblio.ugent.be/publication/8524710/file/8524711.pdf

Enhanced Volatile Organic Compounds emissions and organic aerosol mass increase the oligomer content of atmospheric aerosols

Reduction of structural impacts and distinction of photosynthetic pathways in a global estimation of GPP from space-borne solar-induced chlorophyll fluorescence

H.C. Hansson

Papers

CO₂-induced terrestrial climate feedback mechanism: From carbon sink to aerosol source and back