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Publications

NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.

2017

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Abstract

Increased mineralization of the organic matter (OM) stored in permafrost is expected to constitute the largest additional global warming potential from terrestrial ecosystems exposed to a warmer climate. Chemical composition of permafrost OM is thought to be a key factor controlling the sensitivity of decomposition to warming. Our objective was to characterise OM from permafrost soils of the European Arctic: two mineral soils—Adventdalen, Svalbard, Norway and Vorkuta, northwest Russia— and a ‘‘palsa’’ (ice-cored peat mound patterning in heterogeneous permafrost landscapes) soil in Neiden, northern Norway, in terms of molecular composition and state of decomposition. At all sites, the OM stored in the permafrost was at an advanced stage of decomposition, although somewhat less so in the palsa peat. By comparing permafrost and active layers, we found no consistent effect of depth or permafrost on soil organic matter (SOM) chemistry across sites. The permafrost-affected palsa peat displayed better preservation of plant material in the deeper layer, as indicated by increasing contribution of lignin carbon to total carbon with depth, associated to decreasing acid (Ac) to aldehyde (Al) ratio of the syringyl (S) and vanillyl (V) units, and increasing S/V and contribution of plant-derived sugars. By contrast, in Adventdalen, the Ac/Al ratio of lignin and the Alkyl C to O-alkyl C ratio in the NMR spectra increased with depth, which suggests less oxidized SOM in the active layer compared to the permafrost layer. In Vorkuta, SOM characteristics in the permafrost profile did not change substantially with depth, probably due to mixing of soil layers by cryoturbation. The composition and state of decomposition of SOM appeared to be site-specific, in particular bound to the prevailing organic or mineral nature of soil when attempting to predict the SOM proneness to degradation. The occurrence of processes such as palsa formation in organic soils and cryoturbation should be considered when up-scaling and predicting the responses of OM to climate change in arctic soils.

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Abstract

Empirical evidence based on integrated environmental monitoring including physical, chemical and biological variables is essential for evaluating the ecosystem benefits of costly emission reduction policies. The international multidisciplinary ICP IM (International Cooperative Programme on Integrated Monitoring of Air Pollution Effects on Ecosystems) programme studies the integrated effects of air pollution and climate change on ecosystems in unmanaged and calibrated forested catchments. We calculated site-specific annual input-output budgets for sulphate (SO4) and total inorganic nitrogen (TIN NO3- N + NH4-N) for 17 European ICP IM sites in 1990–2012. Temporal trends for input (deposition) and output (runoff water) fluxes and the net retention/net release of SO4 and TIN were also analysed. Large differences in the input and output fluxes of SO4 and TIN reflect important gradients of air pollution effects in Europe, with the highest deposition and runoff water fluxes at IM sites located in southern Scandinavia and in parts of Central and Eastern Europe and the lowest fluxes at more remote sites in northern European regions. A significant decrease in the total (wet + dry) deposition of non-marine SO4 and bulk deposition of TIN was found at 90% and 65% of the sites, respectively. Output fluxes of non-marine SO4 in runoff decreased significantly at 65% of the sites, indicating positive effects of the international emission abatement actions in Europe during the last 20 years. Catchments retained SO4 in the early and mid1990s, but this shifted towards a net release in the late 1990s, which may be due to the mobilization of legacy S pools accumulated during times of high atmospheric SO4 deposition. Despite decreased deposition, TIN output fluxes and retention rates showed a mixed response with both decreasing (9 sites) and increasing (8 sites) trend slopes, and trends were rarely significant. In general, TIN was strongly retained in the catchments not affected by natural disturbances. The long-term annual variation in net releases for SO4 was explained by variations in runoff and SO4 concentrations in deposition, while a variation in TIN concentrations in runoff was mostly associated with a variation of the TIN retention rate in catchments. The net release of SO4 from forest soils may delay the recovery from acidification for surface waters and the continued enrichment of nitrogen in catchment soils poses a threat to terrestrial biodiversity and may ultimately lead to a higher TIN runoff through N-saturation. Continued monitoring and further evaluations of mass balance budgets are thus needed.