Ongoing and amplified climate change in the Arctic is leading to glacier retreat and to the exposure of an ever-larger portion of non-glaciated permafrost-dominated landscapes. Warming will also cause more precipitation to fall as rain, further enhancing the thaw of previously frozen ground. Yet, the impact of those perturbations on the geochemistry of Arctic rivers remains a subject of debate. Here, we determined the geochemical composition of waters from various contrasting non-glacial permafrost catchments and investigated their impact on a glacially dominated river, the Zackenberg River (Northeast Greenland), during late summer (August 2019). We also studied the effect of rainfall on the geochemistry of the Zackenberg River, its non-glacial tributaries, and a nearby independent non-glacial headwater stream Gr ae nse. We analyzed water properties, quantified and characterized dissolved organic matter (DOM) using absorbance and fluorescence spectroscopy and radiocarbon isotopes, and set this alongside analyses of the major cations (Ca, Mg, Na, and K), dissolved silicon (Si), and germanium/silicon ratios (Ge/Si). The glacier-fed Zackenberg River contained low concentrations of major cations, dissolved Si and dissolved organic carbon (DOC), and a Ge/Si ratio typical of bulk rock. Glacial DOM was enriched in protein-like fluorescent DOM and displayed relatively depleted radiocarbon values (i.e., old DOM). Non-glacial streams (i.e., tributaries and Gr ae nse) had higher concentrations of major cations and DOC and DOM enriched in aromatic compounds. They showed a wide range of values for radiocarbon, Si and Ge/Si ratios associated with variable contributions of surface runoff relative to deep active layer leaching. Before the rain event, Zackenberg tributaries did not contribute notably to the solute export of the Zackenberg River, and supra-permafrost ground waters governed the supply of solutes in Zackenberg tributaries and Gr ae nse stream. After the rain event, surface runoff modified the composition of Gr ae nse stream, and non-glacial tributaries strongly increased their contribution to the Zackenberg River solute export. Our results show that summer rainfall events provide an additional source of DOM and Si-rich waters from permafrost-underlain catchments to the discharge of glacially dominated rivers. This suggests that the magnitude and composition of solute exports from Arctic rivers are modulated by permafrost thaw and summer rain events. This event-driven solute supply will likely impact the carbon cycle in rivers, estuaries, and oceans and should be included into future predictions of carbon balance in these vulnerable Arctic systems.
Rainfall can alter the hydrothermal state of permafrost, subsequently affecting organic carbon decomposition and CO2 transport. However, the mechanisms by which rainfall influences organic carbon decomposition and carbon dioxide transport processes in permafrost remain unclear. In this study, a coupled permafrost water-heatvapor-carbon model, based on the surface energy-water balance theory, is employed to explore the effects of increased precipitation on permafrost moisture, temperature, organic carbon decomposition, and carbon dioxide transport through numerical simulations. The results are as follows: (1) with increased rainfall, surface latent heat flux rises while surface sensible heat flux declines, leading to a reduction in surface heat flux. The annual mean surface heat fluxes for the three precipitation conditions of no change in precipitation (zP = 0 mm), 50 mm increase in precipitation (zP = 50 mm) and 100 mm increase in precipitation (zP = 100 mm) are -0.1 W/m2, -0.2 W/m2 and -0.4 W/m2 respectively; and (2) as rainfall increases, soil moisture content increases significantly, but the impact of rainfall on soil moisture content diminishes with increasing soil depth; and (3) increased rainfall results in a decrease in soil carbon fluxes, soil organic matter decomposition rates, and CO2 concentrations. Compared to the case of constant precipitation, the surface carbon fluxes decreased by 0.04 mu mol center dot m-2s-1 and 0.08 mu mol center dot m-2s-1 under zP = 50 mm and zP = 100 mm, respectively. Additionally, the decomposition rate of soil organic matter at 10 cm depth decreased by 3.2 E-8 mol center dot m-2s-1 and 6.3 E-8 mol center dot m-2s-1, respectively, while the soil carbon concentration decreased by 3 mu mol/mol and 5 mu mol/mol, respectively.
Soil organic carbon (SOC) rapidly accumulates during ecosystem primary succession in glacier foreland. This makes it an ideal model for studying soil carbon sequestration and stabilization, which are urgently needed to mitigate climate change. Here, we investigated SOC dynamics in the Kuoqionggangri glacier foreland on the Tibetan Plateau. The study area along a deglaciation chronosequence of 170-year comprising three ecosystem succession stages, including barren ground, herb steppe, and legume steppe. We quantified amino sugars, lignin phenols, and relative expression of genes associated with carbon degradation to assess the contributions of microbial and plant residues to SOC, and used FT-ICR mass spectroscopy to analyze the composition of dissolved organic matter. We found that herbal plant colonization increased SOC by enhancing ecosystem gross primary productivity, while subsequent legumes development decreased SOC, due to increased ecosystem respiration from labile organic carbon inputs. Plant residues were a greater contributor to SOC than microbial residues in the vegetated soils, but they were susceptible to microbial degradation compared to the more persistent and continuously accumulating microbial residues. Our findings revealed the organic carbon accumulation and stabilization process in early soil development, which provides mechanism insights into carbon sequestration during ecosystem restoration under climate change.
Permafrost stability is significantly influenced by the thermal buffering effects of snow and active-layer peat soils. In the warm season, peat soils act as a barrier to downward heat transfer mainly due to their low thermal conductivity. In the cold season, the snowpack serves as a thermal insulator, retarding the release of heat from the soil to the atmosphere. Currently, many global land models overestimate permafrost soil temperature and active layer thickness (ALT), partially due to inaccurate representations of soil organic matter (SOM) density profiles and snow thermal insulation. In this study, we evaluated the impacts of SOM and snow schemes on ALT simulations at pan-Arctic permafrost sites using the Energy Exascale Earth System Model (E3SM) land model (ELM). We conducted simulations at the Circumpolar Active Layer Monitoring (CALM) sites across the pan-Arctic domain. We improved ELM-simulated site-level ALT using a knowledge-based hierarchical optimization procedure and examined the effects of precipitation-phase partitioning methods (PPMs), snow compaction schemes, and snow thermal conductivity schemes on simulated snow depth, soil temperature, ALT, and CO2 fluxes. Results showed that the optimized ELM significantly improved agreement with observed ALT (e.g. RMSE decreased from 0.83 m to 0.15 m). Our sensitivity analysis revealed that snow-related schemes significantly impact simulated snow thermal insulation levels, soil temperature, and ALT. For example, one of the commonly used snow thermal conductivity schemes (quadratic Sturm or SturmQua) generally produced warmer soil temperatures and larger ALT compared to the other two tested schemes. The SturmQua scheme also amplified the model's sensitivity to PPMs and predicted deeper ALTs than the other two snow schemes under both current and future climates. The study highlights the importance of accurately representing snow-related processes and peat soils in land models to enhance permafrost dynamics simulations.
Permafrost soils in the northern hemisphere are known to harbor large amounts of soil organic matter (SOM). Global climate warming endangers this stable soil organic carbon (SOC) pool by triggering permafrost thaw and deepening the active layer, while at the same time progressing soil formation. But depending, e.g., on ice content or drainage, conditions in the degraded permafrost can range from water-saturated/anoxic to dry/oxic, with concomitant shifts in SOM stabilizing mechanisms. In this field study in Interior Alaska, we investigated two sites featuring degraded permafrost, one water-saturated and the other well-drained, alongside a third site with intact permafrost. Soil aggregate- and density fractions highlighted that permafrost thaw promoted macroaggregate formation, amplified by the incorporation of particulate organic matter, in topsoils of both degradation sites, thus potentially counteracting a decrease in topsoil SOC induced by the permafrost thawing. However, the subsoils were found to store notably less SOC than the intact permafrost in all fractions of both degradation sites. Our investigations revealed up to net 75% smaller SOC storage in the upper 100 cm of degraded permafrost soils as compared to the intact one, predominantly related to the subsoils, while differences between soils of wet and dry degraded landscapes were minor. This study provides evidence that the consideration of different permafrost degradation landscapes and the employment of soil fractionation techniques is a useful combination to investigate soil development and SOM stabilization processes in this sensitive ecosystem.
It is of prime importance to understand feedbacks due to the release of carbon (C) stored in permafrost soils (permafrost-climate feedback) and direct impacts of climatic variations on permafrost dynamics therefore received considerable attention. However, indirect effects of global change, such as the variation in soil nutrient availability and grazing pressure, can alter soil and surface properties of the Arctic tundra, with the potential to modify soil heat transfers toward the permafrost and impact resilience of Arctic ecosystems. We determined the potential of nutrient availability and grazing to alter soil energy balance using a 16-year split-plot experiment crossing fertilization at different doses of nitrogen (N) and phosphorus (P) with protection from goose grazing. Moss biomass and some determinants of the surface energy budget (leaf area index (LAI), dead vascular plant biomass and albedo) were quantified and active layer thaw depth repeatedly measured during three growing seasons. We measured soil physical properties and thermal conductivity and used a physical model to link topsoil organic accumulation processes to heat transfer. Fertilization increased LAI and albedo, whereas grazing decreased dead vascular plant biomass and albedo. Fertilization increased organic accumulation at the top of the soil leading to drier and more porous topsoil, whereas grazing increased water content of topsoil. As a result, topsoil thermal conductivity was higher in grazed plots than in ungrazed ones. Including these properties into a simulation model, we showed that, after 16 years, nutrient addition tended to shallow the active layer whereas grazing deepened mean July active layer by 3.3 cm relative to ungrazed subplots. As a result of OM accumulation at the surface, fertilization increased permafrost vertical aggradation rate by almost an order of magnitude (up to 5 mm year(-1) instead of 0.7 mm year(-1)), whereas grazing slowed down permafrost aggradation by reducing surface uprising and deepening thaw depth. Synthesis. We demonstrated that long-term grazing and N and P addition, through their impact on vegetation and soil properties have the potential to impact permafrost dynamics to the same extent as contemporary temperature increase in High Arctic polygonal wetlands.
Climate warming is predicted to change the fluxes of dissolved organic matter and nitrate by increasing active layer thickness, plant productivity, and organic matter decomposition. These changes are hypothesized to in-crease mineral weathering and soil acidification rates. We investigated whether acidification rates and solute leaching fluxes are variable between permafrost-affected soils with different active layer thicknesses. We compared the fluxes of dissolved organic carbon (DOC) and total dissolved N and the ion fluxes associated with solute leaching and plant uptake to calculate proton budgets in the soils that differed in slope positions (upper slope and lower slope) and soil texture (clayey and sandy soils) in NW Canada. We found the wide variation in DOC and nitrate-N fluxes, depending on slope positions and soil texture. The nitrate-N fluxes were higher at the lower slope position of the sandy soil, compared to the upper slope position. Compared to sandy soils, the DOC fluxes from the organic horizons were higher in the clayey soils on shallower permafrost table. Organic acids were major proton sources in the organic horizons at all sites, but acidity was also contributed by nitrate (sandy and clayey soils at lower slope position) and carbonic acid (clayey soil at upper slope position). The weathering by carbonic acid lead to accumulation of short-range-order minerals in the clayey soils, while incipient podzolization of the sandy soils included the weathering of illite to vermiculite and the dissolution of short-range-order minerals. The shallower active layer thickness at the lower slope position resulted in lower plant productivity and acidification rates. In the permafrost-affected soils, the active layer thickness, the DOC and nitrate-N fluxes, and their contribution to acidification are dependent on the local variation in slope position and soil texture, as well as climate change.
Fluorescence spectroscopy is a commonly used technique to analyze dissolved organic matter in aquatic environments. Given the high sensitivity and non-destructive analysis, fluorescence has recently been used to study water-soluble organic carbon (WSOC) in atmospheric aerosols, which have substantial abundance, various sources and play an important role in climate change. Yet, current research on WSOC characterization is rather sparse and limited to a few isolated sites, making it challenging to draw fundamental and mechanistic conclusions. Here we presented a review of the fluorescence properties of atmospheric WSOC reported in various field and laboratory studies, to discuss the current advances and limitations of fluorescence applications. We highlighted that photochemical reactions and relevant aging processes have profound impacts on fluorescence properties of atmospheric WSOC, which were previously unnoticed for organic matter in aquatic environments. Furthermore, we discussed the differences in sources and chemical compositions of fluorescent components between the atmosphere and hydrosphere. We concluded that the commonly used fluorescence characteristics derived from aquatic environments may not be applicable as references for atmospheric WSOC. We emphasized that there is a need for more systematic studies on the fluorescence properties of atmospheric WSOC and to establish a more robust reference and dataset for fluorescence studies in atmosphere based on extensive source specific experiments. (C) 2020 Elsevier Ltd. All rights reserved.
Arctic permafrost soils store substantial reserves of organic matter (OM) from which microbial transformation contributes significantly to greenhouse gas emissions of CH4 and CO2. However, many younger sediments exposed by glacier retreat and sea level change in fjord landscapes lack significant organic carbon resources, so their capacity to promote greenhouse gas emissions is unclear. We therefore studied the effects of increased temperatures (4 degrees C and 21 degrees C) and OM on rates of Fe(III) reduction, CO2 production, and methanogenesis in three different Holocene sedimentary units from a single site within the former marine limit of Adventdalen, Svalbard. Higher temperature and OM addition generally stimulated CH4 production and CO2 production and an increase in Bacteria and Archaea abundance in all units, whereas an equal stimulation of Fe(II) production by OM amendment and an increase in temperature to 21 degrees C was only observed in a diamicton. We observed an accumulation of Fe(II) in beach and delta deposits as well but saw no stimulating effect of additional OM or increased temperature. Interestingly, we observed a small but significant production of CH4 in all units despite the presence of large reservoirs of Fe(III), sulfate, and nitrate, indicating either the availability of substrates that are primarily used by methanogens or a tight physical coupling between fermentation and methanogenesis by direct electron transfer. Our study clearly illustrates a significant challenge that comes with the large heterogeneity on a narrow spatial scale that one encounters when studying soils that have complex histories.
Accelerated melting of mountain glaciers due to global warming has a significant impact on downstream biogeochemical evolution because a large amount of labile dissolved organic matter (DOM) is released. However, the DOM evolution processes from glacier to downstream are not well understood. To investigate these processes, samples from the glacial surface and terminating runoff of a mountain glacier on the Tibetan Plateau were collected simultaneously throughout the melting season. The samples were analyzed to determine the dissolved organic carbon (DOC) contents and chemical compositions by means of a combination of fluorescence excitation-emission matrix coupled with parallel factor analysis (EEM-PARAFAC) and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The results indicate that the DOC concentrations were higher in the snow samples than in the glacial runoff samples, although a significantly higher concentration of inorganic ions was found in the glacial runoff samples, suggesting the dominant source of DOM in the glacial runoff was the glacier. The EEM-PARAFAC revealed four fluorescent components in both the snow and glacial runoff samples. However, significantly different ratios between the four components of these two categories of samples suggested chemical, physical and/or biological evolution of DOM during transport. Molecular chemical composition analyses by FT-ICR MS revealed that the DOM composition varied dramatically between the glacier and the glacial runoff. More than 50 % of the molecules were transformed from aliphatic and peptide-like compounds in the snow samples into highly unsaturated and phenolic-like compounds in the glacial run-off samples. The potential chemical transformation of DOM was likely related to biological and/or photolytic evolution during transport. Our results suggest that chemical evolution of glacial DOM could occur during the downstream transport, which is expected to be useful for further research exploring the fate of DOM and carbon cycling from the ciyaspheric environment and evaluating the biogeochemical effects.