scholarly journals Future biogeochemical forcing in Eastern Siberia: cooling or warming?

2014 ◽  
Vol 14 (13) ◽  
pp. 19149-19179 ◽  
Author(s):  
A. Arneth ◽  
S. Olin ◽  
R. Makkonen ◽  
P. Paasonen ◽  
T. Holst ◽  
...  

Abstract. Over-proportional warming in the northern high latitudes, and large carbon stocks in boreal and (sub)arctic ecosystems have raised concerns as to whether substantial positive climate feedbacks from biogeochemical process responses should be expected. Such feedbacks occur if increasing temperatures lead to e.g., a net release of CO2 or CH4. However, temperature-enhanced emissions of biogenic volatile organic compounds (BVOC) have been shown to contribute to a cooling feedback via growth of secondary organic aerosol (SOA), and related aerosol forcings. Combining measurements in Eastern Siberia with model-based estimates of vegetation and permafrost dynamics, BVOC emissions and aerosol growth, we show here that the additional climate forcing from changes in ecosystem CO2 balance and BVOC-SOA interactions nearly cancel on a regional scale. The interactions between emissions and vegetation dynamics that underlie individual forcing estimates are complex and highlight the importance of addressing ecosystem-climate feedbacks in consistent, process-based model frameworks that account for a multitude of system processes.

2016 ◽  
Vol 16 (8) ◽  
pp. 5243-5262 ◽  
Author(s):  
Almut Arneth ◽  
Risto Makkonen ◽  
Stefan Olin ◽  
Pauli Paasonen ◽  
Thomas Holst ◽  
...  

Abstract. Disproportional warming in the northern high latitudes and large carbon stocks in boreal and (sub)arctic ecosystems have raised concerns as to whether substantial positive climate feedbacks from biogeochemical process responses should be expected. Such feedbacks occur when increasing temperatures lead, for example, to a net release of CO2 or CH4. However, temperature-enhanced emissions of biogenic volatile organic compounds (BVOCs) have been shown to contribute to the growth of secondary organic aerosol (SOA), which is known to have a negative radiative climate effect. Combining measurements in Eastern Siberia with model-based estimates of vegetation and permafrost dynamics, BVOC emissions, and aerosol growth, we assess here possible future changes in ecosystem CO2 balance and BVOC–SOA interactions and discuss these changes in terms of possible climate effects. Globally, the effects of changes in Siberian ecosystem CO2 balance and SOA formation are small, but when concentrating on Siberia and the Northern Hemisphere the negative forcing from changed aerosol direct and indirect effects become notable – even though the associated temperature response would not necessarily follow a similar spatial pattern. While our analysis does not include other important processes that are of relevance for the climate system, the CO2 and BVOC–SOA interplay serves as an example for the complexity of the interactions between emissions and vegetation dynamics that underlie individual terrestrial processes and highlights the importance of addressing ecosystem–climate feedbacks in consistent, process-based model frameworks.


2015 ◽  
Vol 15 (19) ◽  
pp. 27137-27175
Author(s):  
A. Arneth ◽  
R. Makkonen ◽  
S. Olin ◽  
P. Paasonen ◽  
T. Holst ◽  
...  

Abstract. Disproportional warming in the northern high latitudes, and large carbon stocks in boreal and (sub)arctic ecosystems have raised concerns as to whether substantial positive climate feedbacks from biogeochemical process responses should be expected. Such feedbacks occur if increasing temperatures lead to e.g. a net release of CO2 or CH4. However, temperature-enhanced emissions of biogenic volatile organic compounds (BVOC) have been shown to contribute to the growth of secondary organic aerosol (SOA) which is known to have a negative radiative climate effect. Combining measurements in Eastern Siberia with model-based estimates of vegetation and permafrost dynamics, BVOC emissions and aerosol growth, we assess here possible future changes in ecosystem CO2 balance and BVOC-SOA interactions, and discuss these changes in terms of possible climate effects. On global level, both are very small but when concentrating on Siberia and the northern hemisphere the negative forcing from changed aerosol direct and indirect effects become notable – even though the associated temperature response would not necessarily follow a similar spatial pattern. While our analysis does not include other important processes that are of relevance for the climate system, the CO2 and BVOC-SOA interplay used serves as an example of the complexity of the interactions between emissions and vegetation dynamics that underlie individual terrestrial feedbacks and highlights the importance of addressing ecosystem-climate feedbacks in consistent, process-based model frameworks.


2010 ◽  
Vol 40 (7) ◽  
pp. 1336-1346 ◽  
Author(s):  
E.S. Euskirchen ◽  
A.D. McGuire ◽  
F.S. Chapin ◽  
T.S. Rupp

In the boreal forests of Alaska, recent changes in climate have influenced the exchange of trace gases, water, and energy between these forests and the atmosphere. These changes in the structure and function of boreal forests can then feed back to impact regional and global climates. In this manuscript, we examine the type and magnitude of the climate feedbacks from boreal forests in Alaska. Research generally suggests that the net effect of a warming climate is a positive regional feedback to warming. Currently, the primary positive climate feedbacks are likely related to decreases in surface albedo due to decreases in snow cover. Fewer negative feedbacks have been identified, and they may not be large enough to counterbalance the large positive feedbacks. These positive feedbacks are most pronounced at the regional scale and reduce the resilience of the boreal vegetation – climate system by amplifying the rate of regional warming. Given the recent warming in this region, the large variety of associated mechanisms that can alter terrestrial ecosystems and influence the climate system, and a reduction in the boreal forest resilience, there is a strong need to continue to quantify and evaluate the feedback pathways.


2021 ◽  
Vol 21 (3) ◽  
pp. 1613-1625
Author(s):  
Mike J. Newland ◽  
Daniel J. Bryant ◽  
Rachel E. Dunmore ◽  
Thomas J. Bannan ◽  
W. Joe F. Acton ◽  
...  

Abstract. The impact of emissions of volatile organic compounds (VOCs) to the atmosphere on the production of secondary pollutants, such as ozone and secondary organic aerosol (SOA), is mediated by the concentration of nitric oxide (NO). Polluted urban atmospheres are typically considered to be “high-NO” environments, while remote regions such as rainforests, with minimal anthropogenic influences, are considered to be “low NO”. However, our observations from central Beijing show that this simplistic separation of regimes is flawed. Despite being in one of the largest megacities in the world, we observe formation of gas- and aerosol-phase oxidation products usually associated with low-NO “rainforest-like” atmospheric oxidation pathways during the afternoon, caused by extreme suppression of NO concentrations at this time. Box model calculations suggest that during the morning high-NO chemistry predominates (95 %) but in the afternoon low-NO chemistry plays a greater role (30 %). Current emissions inventories are applied in the GEOS-Chem model which shows that such models, when run at the regional scale, fail to accurately predict such an extreme diurnal cycle in the NO concentration. With increasing global emphasis on reducing air pollution, it is crucial for the modelling tools used to develop urban air quality policy to be able to accurately represent such extreme diurnal variations in NO to accurately predict the formation of pollutants such as SOA and ozone.


Author(s):  
Hind A. A. Al-Abadleh

Extensive research has been done on the processes that lead to the formation of secondary organic aerosol (SOA) including atmospheric oxidation of volatile organic compounds (VOCs) from biogenic and anthropogenic...


2000 ◽  
Vol 13 (12) ◽  
pp. 2002-2010 ◽  
Author(s):  
F. Stuart Chapin ◽  
Werner Eugster ◽  
Joseph P. McFadden ◽  
Amanda H. Lynch ◽  
Donald A. Walker

2013 ◽  
Vol 9 (4) ◽  
pp. 1403-1416 ◽  
Author(s):  
S. Preunkert ◽  
M. Legrand

Abstract. Seasonally resolved chemical ice core records available from the Col du Dôme glacier (4250 m elevation, French Alps), are here used to reconstruct past aerosol load and composition of the free European troposphere from before World War II to present. Available ice core records include inorganic (Na+, Ca2+, NH4+, Cl−, NO3−, and SO42−) and organic (carboxylates, HCHO, humic-like substances, dissolved organic carbon, water-insoluble organic carbon, and black carbon) compounds and fractions that permit reconstructing the key aerosol components and their changes over the past. It is shown that the atmospheric load of submicron aerosol has been increased by a factor of 3 from the 1921–1951 to 1971–1988 years, mainly as a result of a large increase of sulfate (a factor of 5), ammonium and water-soluble organic aerosol (a factor of 3). Thus, not only growing anthropogenic emissions of sulfur dioxide and ammonia have caused the enhancement of the atmospheric aerosol load but also biogenic emissions producing water-soluble organic aerosol. This unexpected change of biospheric source of organic aerosol after 1950 needs to be considered and further investigated in scenarios dealing with climate forcing by atmospheric aerosol.


2019 ◽  
Vol 59 (3) ◽  
Author(s):  
Julija Pauraitė ◽  
Steigvilė Byčenkienė ◽  
Kristina Plauškaitė ◽  
Algirdas Augustaitis ◽  
Vitas Marozas ◽  
...  

Volatile organic compounds (VOCs) emitted by trees in response to abiotic stress evoke high levels of secondary organic aerosol (SOA) compounds. Few techniques exist to provide chemically-resolved submicron (PM1) particle mass concentrations and source apportionment of stress-induced emissions from trees and SOA formation. The chemical composition of atmospheric aerosol particles was characterized using an aerosol chemical speciation monitor (ACSM) at a mixed-mature forest site – the Aukštaitija Integrated Monitoring Station in the eastern part of Lithuania. The organic fraction of PM1 consisted of SOA (76%) and of anthropogenic combustion related primary organic aerosol (POA) (24%). The analysis of tree trunk circumference revealed three shrinkage and three normal increase episodes. During the episodes of tree trunk circumference shrinkage, several m/z signal (m/z 42, 43, 45, 48, 50) intensities were found to be magnified together with the daily SOA concentration. The stress response analysis confirm that tree trunk circumference shrinkage may be observed through the enhancement of selected m/z signals and result in increased SOA levels.


2021 ◽  
Vol 21 (15) ◽  
pp. 11545-11562
Author(s):  
Louise N. Jensen ◽  
Manjula R. Canagaratna ◽  
Kasper Kristensen ◽  
Lauriane L. J. Quéléver ◽  
Bernadette Rosati ◽  
...  

Abstract. This work investigates the individual and combined effects of temperature and volatile organic compound precursor concentrations on the chemical composition of particles formed in the dark ozonolysis of α-pinene. All experiments were conducted in a 5 m3 Teflon chamber at an initial ozone concentration of 100 ppb and initial α-pinene concentrations of 10 and 50 ppb, respectively; at constant temperatures of 20, 0, or −15 ∘C; and at changing temperatures (ramps) from −15 to 20 and from 20 to −15 ∘C. The chemical composition of the particles was probed using a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). A four-factor solution of a positive matrix factorization (PMF) analysis of the combined HR-ToF-AMS data is presented. The PMF analysis and the elemental composition analysis of individual experiments show that secondary organic aerosol particles with the highest oxidation level are formed from the lowest initial α-pinene concentration (10 ppb) and at the highest temperature (20 ∘C). A higher initial α-pinene concentration (50 ppb) and/or lower temperature (0 or −15 ∘C) results in a lower oxidation level of the molecules contained in the particles. With respect to the carbon oxidation state, particles formed at 0 ∘C are more comparable to particles formed at −15 ∘C than to those formed at 20 ∘C. A remarkable observation is that changes in temperature during particle formation result in only minor changes in the elemental composition of the particles. Thus, the temperature at which aerosol particle formation is induced seems to be a critical parameter for the particle elemental composition. Comparison of the HR-ToF-AMS-derived estimates of the content of organic acids in the particles based on m/z 44 in the mass spectra show good agreement with results from off-line molecular analysis of particle filter samples collected from the same experiments. Higher temperatures are associated with a decrease in the absolute mass concentrations of organic acids (R-COOH) and organic acid functionalities (-COOH), while the organic acid functionalities account for an increasing fraction of the measured particle mass.


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