Stockholm university

Sara BlichnerPost doc

About me

I am an atmospheric scientist working on the climate effect of aerosols and clouds using large scale climate models. I have in particular worked on the effect of vegetation through emissions of biogenic volatile organic compounds (BVOCs). In terms of models, I have worked extensively with The Norwegian Earth System Model (NorESM), but I've also done evaluations of EC-Earth, ECHAM-HAM, ECHAM-SALSA and UKESM. I am a researcher at the Stockholm University, and received my PhD from the University of Oslo, Norway, in 2021. I am currently focusing on process evaluation of Earth System Models with the goal of constraining the uncertainty in climate projections.

Publications

A selection from Stockholm University publication database

  • Atmospheric nanoparticle growth

    2023. Dominik Stolzenburg (et al.). Reviews of Modern Physics 95 (4)

    Article

    New particle formation of liquid or solid nanoparticles from gas-phase precursors is a decisive process in Earth’s atmosphere and is considered one of the largest uncertainties in climate change predictions. Key for the climate relevance of new particle formation is the growth of freshly formed molecular clusters, as it determines the survival of these particles to cloud condensation nuclei sizes, where they can contribute to the aerosol-indirect effect. This review lays out the fundamental definitions of nanoparticle growth and addresses the rapidly emerging field of new particle formation studies with a focus on the diverse processes contributing to nanoparticle growth, explicitly comparing the latest experimental findings and their implementation in large-scale models. Atmospheric nanoparticle growth is a complex phenomenon including condensational and reactive vapor uptake, aerosol coagulation, and sink processes. It is linked to thermodynamics, cluster- and phase-transition physics. Nanoparticle growth rates measured from the evolution of the particle-size distribution describe growth as a collective phenomenon, while models often interpret them on a single-particle level and incorporate it into highly simplified size-distribution representations. Recent atmospheric observations show that sulfuric acid together with ammonia and amines, iodic acid, and oxidized organic species can contribute to nanoparticle growth, whereas most models describe the growth effects from a limited subset of this variety of condensable vapors. Atmospheric simulation chamber experiments have clarified the role of ions, intermolecular forces, the interplay of acids and bases, and the contribution of different types of organic vapors. Especially in the complex thermodynamics of organic vapor condensation, the field has had noteworthy advances over the last decade. While the experimental field has achieved significant progress in methodology and process level understanding, this has not led to a similar improvement in the description of the climate impact of nanoparticle formation in large-scale models. This review sets the basis to better align experimental and modeling studies on nanoparticle growth, giving specific guidance for future studies aiming to resolve the questions as to why the climate response in large-scale models seems to be buffered against high survival probabilities and why the global growth observations herein show surprisingly low variation.

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  • Process-evaluation of forest aerosol-cloud-climate feedback shows clear evidence from observations and large uncertainty in models

    2024. Sara M. Blichner (et al.). Nature Communications 15

    Article

    Natural aerosol feedbacks are expected to become more important in the future, as anthropogenic aerosol emissions decrease due to air quality policy. One such feedback is initiated by the increase in biogenic volatile organic compound (BVOC) emissions with higher temperatures, leading to higher secondary organic aerosol (SOA) production and a cooling of the surface via impacts on cloud radiative properties. Motivated by the considerable spread in feedback strength in Earth System Models (ESMs), we here use two long-term observational datasets from boreal and tropical forests, together with satellite data, for a process-based evaluation of the BVOC-aerosol-cloud feedback in four ESMs. The model evaluation shows that the weakest modelled feedback estimates can likely be excluded, but highlights compensating errors making it difficult to draw conclusions of the strongest estimates. Overall, the method of evaluating along process chains shows promise in pin-pointing sources of uncertainty and constraining modelled aerosol feedbacks.

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  • Potential pre-industrial–like new particle formation induced by pure biogenic organic vapors in Finnish peatland

    2024. Wei Huang (et al.). Science Advances 10 (14)

    Article

    Pure biogenic new particle formation (NPF) induced by highly oxygenated organic molecules (HOMs) could be an important mechanism for pre-industrial aerosol formation. However, it has not been unambiguously confirmed in the ambient due to the scarcity of truly pristine continental locations in the present-day atmosphere or the lack of chemical characterization of NPF precursors. Here, we report ambient observations of pure biogenic HOM-driven NPF over a peatland in southern Finland. Meteorological decoupling processes formed an “air pocket” (i.e., a very shallow surface layer) at night and favored NPF initiated entirely by biogenic HOM from this peatland, whose atmospheric environment closely resembles that of the pre-industrial era. Our study sheds light on pre-industrial aerosol formation, which represents the baseline for estimating the impact of present and future aerosol on climate, as well as on future NPF, the features of which may revert toward pre-industrial–like conditions due to air pollution mitigation.

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  • Constraining global transport of perfluoroalkyl acids on sea spray aerosol using field measurements

    2024. Bo Sha (et al.). Science Advances 10 (14)

    Article

    Perfluoroalkyl acids (PFAAs) are highly persistent anthropogenic pollutants that have been detected in the global oceans. Our previous laboratory studies demonstrated that PFAAs in seawater are remobilized to the air in sea spray aerosols (SSAs). Here, we conducted field experiments along a north-south transect of the Atlantic Ocean to study the enrichment of PFAAs in SSA. We show that in some cases PFAAs were enriched >100,000 times in the SSA relative to seawater concentrations. On the basis of the results of the field experiments, we estimate that the secondary emission of certain PFAAs from the global oceans via SSA emission is comparable to or greater than estimates for the other known global sources of PFAAs to the atmosphere from manufacturing emissions and precursor degradation.

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Show all publications by Sara Blichner at Stockholm University