Riverine transport of biogenic elements to the Baltic Sea ? past and possible future perspectives

International audienceThe paper reviews critical processes for the land-sea fluxes of biogenic elements (C, N, P, Si) in the Baltic Sea catchment and discusses possible future scenarios as a consequence of improved sewage treatment, agricultural practices and increased hydropower demand (for N, P and Si) and of global warming, i.e., changes in hydrological patterns (for C). These most significant drivers will not only change the total amount of nutrient inputs and fluxes of organic and inorganic forms of carbon to the Baltic Sea, their ratio (C:N:P:Si) will alter as well with consequences for phytoplankton species composition in the Baltic Sea. In summary, we propose that N fluxes may increase due to higher livestock densities in those countries recently acceded to the EU, whereas P and Si fluxes may decrease due to an improved sewage treatment in these new EU member states and with further damming and still eutrophic states of many lakes in the entire Baltic Sea catchment. This might eventually decrease cyanobacteria blooms in the Baltic but increase the potential for other nuisance blooms. Dinoflagellates could eventually substitute diatoms that even today grow below their optimal growth conditions due to low Si concentrations in some regions of the Baltic Sea. C fluxes will probably increase from the boreal part of the Baltic Sea catchment due to the expected higher temperatures and heavier rainfall. However, it is not clear whether dissolved organic carbon and alkalinity, which have opposite feedbacks to global warming, will increase in similar amounts, because the spring flow peak will be smoothed out in time due to higher temperatures that cause less snow cover and deeper soil infiltration

Remineralization rate of terrestrial DOC as inferred from CO2 supersaturated coastal waters

Coastal seas receive large amounts of terrestrially derived organic carbon (OC). The fate of this carbon, and its impact on the marine environment, is however poorly understood. Here we combine underway CO2 partial pressure (pCO(2)) measurements with coupled 3-D hydrodynamical-biogeochemical modelling to investigate whether remineralization of terrestrial dissolved organic carbon (tDOC) can explain CO2 supersaturated surface waters in the Gulf of Bothnia, a subarctic estuary. We find that a substantial remineralization of tDOC and a strong tDOC-induced light attenuation dampening the primary production are required to reproduce the observed CO2 supersaturated waters in the nearshore areas. A removal rate of tDOC of the order of 1 year, estimated in a previous modelling study in the same area, gives a good agreement between modelled and observed pCO(2). The remineralization rate is on the same order as bacterial degradation rates calculated from published incubation experiments, suggesting that bacteria has the potential to cause this degradation. Furthermore, the observed high pCO(2) values during the ice-covered season argue against photochemical degradation as the main removal mechanism. All of the remineralized tDOC is outgassed to the atmosphere in the model, turning the northernmost part of the Gulf of Bothnia into a source of CO2 to the atmosphere.peerReviewe

Weathering rates and origin of inorganic carbon as influenced by river regulation in the boreal sub-arctic region of Sweden

International audienceMajor environmental stressors of boreal and sub-arctic rivers are hydrological changes and global warming and both factors will significantly influence the future evolution of the river chemistry in high latitudes. We tested the hypothesis whether lower concentrations of dissolved constituents observed in regulated rivers come along with lower weathering rates, though specific discharge as a major force for physical erosion and weathering is often higher in regulated river systems. In this study the river chemistry, weathering rates and related carbon dioxide consumption in two large watersheds in the sub arctic region of Sweden, one regulated river (Lule River) and one unregulated river (Kalix River), was investigated. Weathering rates of silicates in the two watersheds are shown to be different; the silicate weathering rate in Kalix River catchment is almost 30% higher than in the Lule River catchment. This is most likely a result of constructing large reservoirs in the former river valleys inundating the alluvial deposits and thus decreasing soil/water contact resulting in lower weathering rates. Furthermore, the difference observed in weathering rates between lowland regions and headwaters suggests that weathering in sub arctic boreal climates is controlled by the residence time for soil water rock interactions followed by lithology. The chemistry in the two rivers shows weathering of silicates as the origin for 68% of the inorganic carbon in the Lule River and 74% for Kalix River. The study clearly shows that river regulation significantly decreases alkalinity export to the sea because lower weathering rates gives less carbon dioxide ending up as DIC. By considering sources for inorganic carbon we here report that the inorganic carbon load that originates from respiration of organic matter in soils makes up of 30% and 35% of the total C export for the watersheds of the Kalix River and Lule River, respectively. Therefore, both the inorganic (i.e. the origin of carbon in DIC) and organic carbon load carbon must be considered when studying climate changes on the organic carbon load since effects from increased degradation of organic matter may lead to more weathering (higher production of DIC)

River biogeochemistry and source identification of nitrate by means of isotopic tracers in the Baltic Sea catchments

International audienceNitrate input to a river is largely controlled by land use in its catchment. We compared the information carried by the isotopic signatures of nitrate in 12 Baltic rivers, in relation to the vegetation cover of their catchments. We found isotope values in nitrate ranging from ?2 to 14 for ?15N and 8 to 25 per mil for ?18O. Seasonal signals were evident in all rivers. The annual variability of riverine isotope signatures is presented in detail for one Nordic, the Kemijoki, and two southern rivers, Vistula and Oder. Nordic rivers with relatively pristine vegetation in its catchments show not only low ?15N values and high ?18O-NO3? but also lower annual variability than rivers draining densely populated land. Seasonal signals could be found in all of the rivers. We used load weighted nitrate isotope data and data from the three major sources (farmland/sewage, atmospheric deposition and from runoff of pristine soils) to theoretically estimate the shares of nitrate from these sources. The results agree well with same estimates derived from a Global Land Cover data base. The comparison with an emission model (EM) reveals good agreements for intensively used catchments and rather bad ones for pristine catchments. Advantages and limitations of the tested model types are discussed

Landscape elements and river chemistry as affected by river regulation – a 3-D perspective

We tested the hypothesis whether individual land classes within a river catchment contribute equally to river loading with dissolved constituents or whether some land classes act as "hot spots" to river loading and if so, are these land classes especially affected by hydrological alterations. The amount of land covered by forests and wetlands and the average soil depth (throughout this paper soil refers to everything overlying bedrock i.e. regolith) of a river catchment explain 58–93% of the variability in total organic carbon (TOC) and dissolved silicate (DSi) concentrations for 22 river catchments in Northern Sweden. For the heavily regulated Luleälven, with 7 studied sub-catchments, only 3% of the headwater areas have been inundated by reservoirs, some 10% of the soils and aggregated forest and wetland areas have been lost due to damming and further hydrological alteration such as bypassing entire sub-catchments by headrace tunnels. However, looking at individual forest classes, our estimates indicate that some 37% of the deciduous forests have been inundated by the four major reservoirs built in the Luleälven headwaters. These deciduous forest and wetlands formerly growing on top of alluvial deposits along the river corridors forming the riparian zone play a vital role in loading river water with dissolved constituents, especially DSi. A digital elevation model draped with land classes and soil depths which highlights that topography of various land classes acting as hot spots is critical in determining water residence time in soils and biogeochemical fluxes. Thus, headwater areas of the Luleälven appear to be most sensitive to hydrological alterations due to the thin soil cover (on average 2.7–4.5 m) and only patchy appearance of forest and wetlands that were significantly perturbed. Hydrological alterations of these relatively small headwater areas significantly impacts downstream flux of dissolved constituents and their delivery to receiving water bodies

Estimation of permafrost thawing rates in a sub-arctic catchment using recession flow analysis

Permafrost thawing is likely to change the flow pathways taken by water as it moves through arctic and sub-arctic landscapes. The location and distribution of these pathways directly influence the carbon and other biogeochemical cycling in northern latitude catchments. While permafrost thawing due to climate change has been observed in the arctic and sub-arctic, direct observations of permafrost depth are difficult to perform at scales larger than a local scale. Using recession flow analysis, it may be possible to detect and estimate the rate of permafrost thawing based on a long-term streamflow record. We demonstrate the application of this approach to the sub-arctic Abiskojokken catchment in northern Sweden. Based on recession flow analysis, we estimate that permafrost in this catchment may be thawing at an average rate of about 0.9 cm/yr during the past 90 years. This estimated thawing rate is consistent with direct observations of permafrost thawing rates, ranging from 0.7 to 1.3 cm/yr over the past 30 years in the region

Direct determination of the air-sea CO₂ gas transfer velocity in Arctic sea-ice regions

The Arctic Ocean is an important sink for atmospheric CO₂. The impact of decreasing sea-ice extent and expanding marginal ice zones on Arctic air-sea CO₂ exchange depends on the rate of gas transfer in the presence of sea ice. Sea ice acts to limit air-sea gas exchange by reducing contact between air and water, but is also hypothesised to enhance gas transfer rates across surrounding open water surfaces through physical processes such as increased surface-ocean turbulence from ice-water shear and ice-edge form drag. Here we present the first direct determination of the CO₂ air-sea gas transfer velocity in a wide range of Arctic sea-ice conditions. We show that the gas transfer velocity increases near-linearly with decreasing sea-ice concentration. We also show that previous modeling approaches overestimate gas transfer rates in sea-ice regions

High spatiotemporal variability of methane concentrations challenges estimates of emissions across vegetated coastal ecosystems

Coastal methane (CH4) emissions dominate the global ocean CH4 budget and can offset the "blue carbon" storage capacity of vegetated coastal ecosystems. However, current estimates lack systematic, high-resolution, and long-term data from these intrinsically heterogeneous environments, making coastal budgets sensitive to statistical assumptions and uncertainties. Using continuous CH4 concentrations, delta C-13-CH4 values, and CH4 sea-air fluxes across four seasons in three globally pervasive coastal habitats, we show that the CH4 distribution is spatially patchy over meter-scales and highly variable in time. Areas with mixed vegetation, macroalgae, and their surrounding sediments exhibited a spatiotemporal variability of surface water CH4 concentrations ranging two orders of magnitude (i.e., 6-460 nM CH4) with habitat-specific seasonal and diurnal patterns. We observed (1) delta C-13-CH signatures that revealed habitat-specific CH4 production and consumption pathways, (2) daily peak concentration events that could change >100% within hours across all habitats, and (3) a high thermal sensitivity of the CH4 distribution signified by apparent activation energies of similar to 1 eV that drove seasonal changes. Bootstrapping simulations show that scaling the CH4 distribution from few samples involves large errors, and that similar to 50 concentration samples per day are needed to resolve the scale and drivers of the natural variability and improve the certainty of flux calculations by up to 70%. Finally, we identify northern temperate coastal habitats with mixed vegetation and macroalgae as understudied but seasonally relevant atmospheric CH4 sources (i.e., releasing >= 100 mu mol CH4 m(-2) day(-1) in summer). Due to the large spatial and temporal heterogeneity of coastal environments, high-resolution measurements will improve the reliability of CH4 estimates and confine the habitat-specific contribution to regional and global CH4 budgets.Peer reviewe

Source identification of nitrate by means of isotopic tracers in the Baltic Sea catchments

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Methane emissions offset atmospheric carbon dioxide uptake in coastal macroalgae, mixed vegetation and sediment ecosystems

Publisher Copyright: © 2023, The Author(s).Coastal ecosystems can efficiently remove carbon dioxide (CO2) from the atmosphere and are thus promoted for nature-based climate change mitigation. Natural methane (CH4) emissions from these ecosystems may counterbalance atmospheric CO2 uptake. Still, knowledge of mechanisms sustaining such CH4 emissions and their contribution to net radiative forcing remains scarce for globally prevalent macroalgae, mixed vegetation, and surrounding depositional sediment habitats. Here we show that these habitats emit CH4 in the range of 0.1 – 2.9 mg CH4 m−2 d−1 to the atmosphere, revealing in situ CH4 emissions from macroalgae that were sustained by divergent methanogenic archaea in anoxic microsites. Over an annual cycle, CO2-equivalent CH4 emissions offset 28 and 35% of the carbon sink capacity attributed to atmospheric CO2 uptake in the macroalgae and mixed vegetation habitats, respectively, and augment net CO2 release of unvegetated sediments by 57%. Accounting for CH4 alongside CO2 sea-air fluxes and identifying the mechanisms controlling these emissions is crucial to constrain the potential of coastal ecosystems as net atmospheric carbon sinks and develop informed climate mitigation strategies.Peer reviewe