High-latitude mires store a considerable part of the global soil carbon. Current understanding suggests that wetter conditions promote carbon accumulation. This paradigm is based primarily on temperate ombrogenic bogs and overlooks the influence of minerogenic water from the catchment area, despite most northern mires being minerogenic fens. Here we show that minerogenic water is the main negative influence on past century carbon accumulation in boreal fens. This effect is most pronounced in mires formed during the last millennia. Rather than enhancing productivity, minerogenic water stimulates organic matter decay, apart from in elevated hummocks where both decay and productivity were stimulated. These findings reshape our understanding of carbon cycling at high-latitudes, highlighting how shifts in precipitation-evapotranspiration may impact carbon sequestration in fens, which are widespread in the circum-arctic. Contrary to expectations for temperate regions, we argue that increased catchment water input in sub-arctic peatlands is unlikely to enhance mire carbon accumulation.

The consequences of permafrost thaw for organic carbon release are mainly studied in summer, considering the frozen soil is inert in winter. Here, we show that biogeochemical processes also occur during early winter. We combine Si isotopes and Ge/Si with Fe and dissolved organic carbon (DOC) concentrations in soil porewater along a natural gradient of permafrost degradation (palsa, intermediate and degraded palsa sites) and in river water (Stordalen, Sweden) collected during late autumn and early winter. The data support: (i) the occurrence of early winter snowmelt water infiltration in soils diluting more extensively the soil porewater in dry well-drained palsa soils; (ii) the decrease of the redox potential (by 30 %) induced by snowmelt water infiltration and water table rise at the intermediate site, favouring Fe-oxides dissolution and the release of the associated DOC in soil porewater; (iii) the contribution of snowmelt water infiltration to the Fe and DOC lateral export from permafrost degrading soils to rivers.

Coastal areas are an important source of methane (CH4). However, the exact origins of CH4 in the surface waters of coastal regions, which in turn drive sea-air emissions, remain uncertain. To gain a comprehensive understanding of the current and future climate change feedbacks, it is crucial to identify these CH4 sources and processes that regulate its formation and oxidation. This study investigated coastal CH4 dynamics by comparing water column data from six stations located in the brackish Tvärminne Archipelago, Baltic Sea. The sediment biogeochemistry and microbiology were further investigated at two stations (i.e., nearshore and offshore). These stations differed in terms of stratification, bottom water redox conditions, and organic matter loading. At the nearshore station, CH4 diffusion from the sediment into the water column was negligible, because nearly all CH4 was oxidized within the upper sediment column before reaching the sediment surface. On the other hand, at the offshore station, there was significant benthic diffusion of CH4, albeit the majority underwent oxidation before reaching the sediment-water interface, due to shoaling of the sulfate methane transition zone (SMTZ). The potential contribution of CH4 production in the water column was evaluated and was found to be negligible. After examining the isotopic signatures of δ13C-CH4 across the sediment and water column, it became apparent that the surface water δ13C-CH4 values observed in areas with thermal stratification could not be explained by diffusion, advective fluxes, nor production in the water column. In fact, these values bore a remarkable resemblance to those detected below the SMTZ. This supports the hypothesis that the source of CH4 in surface waters is more likely to originate from ebullition than diffusion in stratified brackish coastal systems.

Submarine groundwater discharge (SGD) is an important process responsible for transporting terrestrial dissolved chemical substances into the coastal ocean, thereby impacting the marine ecosystem. Despites its significance, there are few studies addressing SGD in the northern Baltic Sea. Here we investigate the potential occurrence of SGD in an area characterized by seafloor terraces formed in varved glacial clay located around Fifång Island, Southern Stockholm Archipelago. We analyzed 222Rn activity and porewater geochemistry in both marine and terrestrial sediment cores retrieved from Fifång Island and its surrounding offshore areas. Results from 222Rn mass-balance calculations, water isotopes, salinity, chloride concentration, and dating (including 14C and helium-tritium dating) indicate that modern groundwater flows through varved glacial clay layers and fractured rocks on Fifång Island and discharges into Fifång Bay. Additionally, the offshore cores reveal a saline groundwater source that, dating of the dissolved inorganic carbon, appears systematically younger than the hosting clay varves dated using the Swedish clay varve chronology. Acoustic blanking in our acquired sub-bottom profiles may be related to this fluid migration. The occurrence of this saline groundwater seems to be independent from the distance to the submarine terraces. Collectively, our study confirms the occurrence of submarine groundwater in the varved glacial clay close to Fifång Island and further offshore. Our findings help establish the significance of submarine groundwater discharge in influencing the past and present coastal environment in the Baltic Sea region.

Sea-ice dynamics can affect carbon cycling in polar oceans, with sea-ice ikaite acting as a potentially important carbon pump. However, there is no large-scale direct field evidence to support this. Here we used a unique data set that combined continuous measurements of atmospheric and water CO2 concentrations with water chemistry data collected over 1,200 km along the East Siberian Sea, the widest Arctic shelf sea. Our results reveal large spatial heterogeneity of sea-ice ikaite contents, which directly interact with carbonate chemistry in the water column. Our findings demonstrate that the CO2 drawdown by sea-ice ikaite dissolution could be as important as that by primary production. We suggest that the role of ikaite in regulating the seasonal carbon cycle on a regional scale could be more important than we previously thought. Effects of the warmer climate on sea ice loss might also play a role in the ikaite inventory.

An advance has been made towards a method for forecasting earthquakes several months before they occur. The method relies on changes of groundwater chemistry as earthquake precursors. In a study published in 2014, we showed that changes of groundwater chemistry occurred prior to and were associated with two earthquakes of magnitude 5 and higher, which affected northern Iceland in 2012 and 2013. Here we test the hypothesis that similar or larger earthquakes could have been forecast in the following decade (i.e. 2014–2023) based on our published findings. We found that we could have forecast one of the three greater than magnitude 5 earthquakes that occurred. Noting that changes of groundwater chemistry were oscillatory, we infer expansion and contraction of the groundwater source region caused by coupled crustal dilation and fracture mineralisation associated with the stress build-up before earthquakes. We conclude by proposing how our approach could be implemented elsewhere.

Elevated manganese (Mn) concentration in many drinking water tubewells in Bangladesh has made access to safe drinking water more critical despite providing arsenic (As) safe water to millions of people after decades of efforts to achieve latter. This study evaluates the potential of the Intermediate Deep Aquifer (IDA) in the Matlab area of Bangladesh as a source of As-safe and low-Mn groundwater. Based on observations from depth-specific piezometer nests, drinking water tubewells were installed at a targeted depth of 120 m in the Matlab region, an As-hot spot in the country. Water chemistry analysis of 243 Intermediate Deep Tubewells (IDTW) provided promising results which support the strategy of exploiting the IDA as a safe source for drinking water tubewells. Arsenic, manganese and other trace elements, along with the major ions, were analyzed by high-precision ICP-OES and ion chromatography. The Bangladesh drinking water standard for As (50 μg/L) was exceeded only in 3 wells (1%) while 99% (n = 240) of the wells were found to be safe. More than 91% (n = 222) were within the WHO guideline value of 10 μg/L. For Mn, 89% (n = 217) of the wells showed the concentration within or below the former WHO guideline value of 0.4 mg/L with a mean and median value of 0.18 and 0.07 mg/L respectively. Similar high permeability sand units at this depth range, if available could be targeted by the local tubewell drillers for tapping water at half the cost of deep tubewell installation, which will be quite encouraging for the local community, considering their affordability for installation of As-safe and low-Mn drinking water tubewells. This study's results could also be important for other relevant stakeholders, including the policy makers, implementing agencies and the water sector development partners, as well as water supply projects elsewhere in the world with similar hydrogeological settings.

Vegetation holds the key to many properties that make natural mires unique, such as surface microtopography, high biodiversity values, effective carbon sequestration and regulation of water and nutrient fluxes across the landscape. Despite this, landscape controls behind mire vegetation patterns have previously been poorly described at large spatial scales, which limits the understanding of basic drivers underpinning mire ecosystem services. We studied catchment controls on mire nutrient regimes and vegetation patterns using a geographically constrained natural mire chronosequence along the isostatically rising coastline in Northern Sweden. By comparing mires of different ages, we can partition vegetation patterns caused by long-term mire succession (<5000 years) and present-day vegetation responses to catchment eco-hydrological settings. We used the remote sensing based normalized difference vegetation index (NDVI) to describe mire vegetation and combined peat physicochemical measures with catchment properties to identify the most important factors that determine mire NDVI. We found strong evidence that mire NDVI depends on nutrient inputs from the catchment area or underlying mineral soil, especially concerning phosphorus and potassium concentrations. Steep mire and catchment slopes, dry conditions and large catchment areas relative to mire areas were associated with higher NDVI. We also found long-term successional patterns, with lower NDVI in older mires. Importantly, the NDVI should be used to describe mire vegetation patterns in open mires if the focus is on surface vegetation, since the canopy cover in tree-covered mires completely dominated the NDVI signal. With our study approach, we can quantitatively describe the connection between landscape properties and mire nutrient regime. Our results confirm that mire vegetation responds to the upslope catchment area, but importantly, also suggest that mire and catchment aging can override the role of catchment influence. This effect was clear across mires of all ages, but was strongest in younger mires.

Large Arctic rivers are an important source of iron (Fe) to the Arctic Ocean, though seasonal variations in the terrestrial source and supply of Fe to the ocean are unknown. To constrain the seasonal variability, we present Fe concentrations and isotopic compositions (δ⁵⁶Fe) for particulate (>0.22 µm) and colloidal (<0.22 µm–1 kDa) Fe from the Lena River, NE Russia. Samples were collected every month during winter baseflow (September 2012–March 2013) and every 2–3 days before, during and after river ice break-up (May 2015).

Iron in particles have isotope ratios lower than crustal values during winter (e.g., δ⁵⁶Fe_Part = −0.37 ± 0.16‰), and crustal-like values during river ice break-up and spring flood (e.g., δ⁵⁶Fe_Part = 0.07 ± 0.08‰), indicating a change in the source of particulate Fe between winter and spring flood. Low isotope values are indicative of mineral dissolution, transport of reduced Fe in sub-oxic, ice-covered sub-permafrost groundwaters and near-quantitative precipitation of Fe as particles. Crustal-like isotopic compositions result from the increased supply of detrital particles from riverbank and soil erosion during river ice break-up and flooding. Iron colloids (<0.22 μm) have δ⁵⁶Fe values that are comparable to or lower than crustal values during winter (e.g., δ⁵⁶Fe_Col = −0.08 ± 0.05‰) but similar to or higher than crustal values during spring flood (e.g., δ⁵⁶Fe_Col= +0.24 ± 0.11‰). Low δ⁵⁶Fe ratios for colloidal Fe during winter are consistent with precipitation from isotopically light Fe(II)_aq transported in sub-permafrost groundwaters. Higher colloidal δ⁵⁶Fe ratios during the spring flood indicate that these colloids are supplied from surface soils, where Fe is fractionated via oxidation or organic carbon complexation, similar to during summer. Approximately half of the annual colloidal Fe flux occurs during spring flood while most of the remaining colloidal Fe is supplied during summer months. The total amount of colloidal Fe transported during winter was relatively low. The seasonal variation in colloidal Fe isotope values may be a useful tool to trace the source of colloidal Fe to the Arctic Ocean and monitor future changes in the sources and supply of Fe from the permafrost landscape to the Lena River basin.

Microbial sulfate reduction (MSR), which transforms sulfate into sulfide through the consumption of organic matter, is an integral part of sulfur and carbon cycling. Yet, the knowledge on MSR magnitudes is limited and mostly restricted to snap-shot conditions in specific surface water bodies. Potential impacts of MSR have consequently been unaccounted for, e.g., in regional or global weathering budgets. Here, we synthesize results from previous studies on sulfur isotope dynamics in stream water samples and apply a sulfur isotopic fractionation and mixing scheme combined with Monte Carlo simulations to derive MSR in entire hydrological catchments. This allowed comparison of magnitudes both within and between five study areas located between southern Sweden and the Kola Peninsula, Russia. Our results showed that the freshwater MSR ranged from 0 to 79 % (interquartile range of 19 percentage units) locally within the catchments, with average values from 2 to 28 % between the catchments, displaying a non-negligible catchment-average value of 13 %. The combined abundance or deficiency of several landscape elements (e.g., the areal percentage of forest and lakes/wetlands) were found to indicate relatively well whether or not catchment-scale MSR would be high. A regression analysis showed specifically that average slope was the individual element that best reflected the MSR magnitude, both at sub-catchment scale and between the different study areas. However, the regression results of individual parameters were generally weak. The MSR-values additionally showed differences between seasons, in particular in wetland/lake dominated catchments. Here MSR was high during the spring flood, which is consistent with the mobilization of water that under low-flow winter periods have developed the needed anoxic conditions for sulfate-reducing microorganisms. This study presents for the first time compelling evidence from multiple catchments of wide-spread MSR at levels slightly above 10 %, implying that the terrestrial pyrite oxidation may be underestimated in global weathering budgets.