Variation in the seston C:N ratio of the Arctic Ocean and pan-Arctic shelves

Studying more than 3600 observations of particulate organic carbon (POC) and particulate organic nitrogen (PON), we evaluate the applicability of the classic Redfield C:N ratio (6.6) and the recently proposed Sterner ratio (8.3) for the Arctic Ocean and pan-Arctic shelves. The confidence intervals for C:N ranged from 6.43 to 8.82, while the average C:N ratio for all observations was 7.4. In general, neither the Redfield or Sterner ratios were applicable, with the Redfield ratio being too low and the Sterner ratio too high. On a regional basis, all northern high latitude regions had a C:N ratio significantly higher than the Redfield ratio, except the Arctic Ocean (6.6), Chukchi (6.4) and East Siberian (6.5) Seas. The latter two regions were influenced by nutrient-rich Pacific waters, and had a high fraction of autotrophic (i.e. algal-derived) material. The C:N ratios of the Laptev (7.9) and Kara (7.5) Seas were high, and had larger contributions of terrigenous material. The highest C:N ratios were in the North Water (8.7) and Northeast Water (8.0) polynyas, and these regions were more similar to the Sterner ratio. The C:N ratio varied between regions, and was significantly different between the Atlantic (6.7) and Arctic (7.9) influenced regions of the Barents Sea, while the Atlantic dominated regions (Norwegian, Greenland and Atlantic Barents Seas) were similar (6.7–7). All observations combined, and most individual regions, showed a pattern of decreasing C:N ratios with increasing seston concentrations. This meta-analysis has important implications for ecosystem modelling, as it demonstrated the striking temporal and spatial variability in C:N ratios and challenges the common assumption of a constant C:N ratio. The non-constant stoichiometry was believed to be caused by variable contributions of autotrophs, heterotrophs and detritus to seston, and a significant decrease in C:N ratios with increasing Chlorophyll a concentrations supports this view. This study adds support to the use of a power function model, where the exponent is system-specific, but we suggest a general Arctic relationship, where POC = 7.4 PON0.89

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrainedMethane release from open leads and new ice following an Arctic winter storm eventacceptedVersio

Enhanced CO2 uptake at a shallow Arctic Ocean seep field overwhelms the positive warming potential of emitted methane

Source at https://doi.org/10.1073/pnas.1618926114.Continued warming of the Arctic Ocean in coming decades is projected to trigger the release of teragrams (1 Tg = 106 tons) of methane from thawing subsea permafrost on shallow continental shelves and dissociation of methane hydrate on upper continental slopes. On the shallow shelves (<100 m water depth), methane released from the seafloor may reach the atmosphere and potentially amplify global warming. On the other hand, biological uptake of carbon dioxide (CO2) has the potential to offset the positive warming potential of emitted methane, a process that has not received detailed consideration for these settings. Continuous sea−air gas flux data collected over a shallow ebullitive methane seep field on the Svalbard margin reveal atmospheric CO2 uptake rates (−33,300 ± 7,900 μmol m−2⋅d−1) twice that of surrounding waters and ∼1,900 times greater than the diffusive sea−air methane efflux (17.3 ± 4.8 μmol m−2⋅d−1). The negative radiative forcing expected from this CO2 uptake is up to 231 times greater than the positive radiative forcing from the methane emissions. Surface water characteristics (e.g., high dissolved oxygen, high pH, and enrichment of 13C in CO2) indicate that upwelling of cold, nutrient-rich water from near the seafloor accompanies methane emissions and stimulates CO2 consumption by photosynthesizing phytoplankton. These findings challenge the widely held perception that areas characterized by shallow-water methane seeps and/or strongly elevated sea−air methane flux always increase the global atmospheric greenhouse gas burden

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrained

Marine CDOM accumulation during a coastal Arctic mesocosm experiment: No response to elevated pCO2levels

A large-scale multidisciplinary mesocosm experiment in an Arctic fjord (Kongsfjorden, Svalbard; 78°56.2′N) was used to study Arctic marine food webs and biogeochemical elements cycling at natural and elevated future carbon dioxide (CO2) levels. At the start of the experiment, marine-derived chromophoric dissolved organic matter (CDOM) dominated the CDOM pool. Thus, this experiment constituted a convenient case to study production of autochthonous CDOM, which is typically masked by high levels of CDOM of terrestrial origin in the Arctic Ocean proper. CDOM accumulated during the experiment in line with an increase in bacterial abundance; however, no response was observed to increased pCO2 levels. Changes in CDOM absorption spectral slopes indicate that bacteria were most likely responsible for the observed CDOM dynamics. Distinct absorption peaks (at ~ 330 and ~ 360 nm) were likely associated with mycosporine-like amino acids (MAAs). Due to the experimental setup, MAAs were produced in absence of ultraviolet exposure providing evidence for MAAs to be considered as multipurpose metabolites rather than simple photoprotective compounds. We showed that a small increase in CDOM during the experiment made it a major contributor to total absorption in a range of photosynthetically active radiation (PAR, 400–700 nm) and, therefore, is important for spectral light availability and may be important for photosynthesis and phytoplankton groups composition in a rapidly changing Arctic marine ecosystem

Seasonal shifts of microbial methane oxidation in Arctic shelf waters above gas seeps

The Arctic Ocean subseabed holds vast reservoirs of the potent greenhouse gas methane (CH4), often seeping into the ocean water column. In a continuously warming ocean as a result of climate change an increase of CH4 seepage from the seabed is hypothesized. Today, CH4 is largely retained in the water column due to the activity of methane-oxidizing bacteria (MOB) that thrive there. Predicted future oceanographic changes, bottom water warming and increasing CH4 release may alter efficacy of this microbially mediated CH4 sink. Here we investigate the composition and principle controls on abundance and activity of the MOB communities at the shallow continental shelf west of Svalbard, which is subject to strong seasonal changes in oceanographic conditions. Covering a large area (364 km2), we measured vertical distribution of microbial methane oxidation (MOx) rates, MOB community composition, dissolved CH4 concentrations, temperature and salinity four times throughout spring and summer during three consecutive years. Sequencing analyses of the pmoA gene revealed a small, relatively uniform community mainly composed of type-Ia methanotrophs (deep-sea 3 clade). We found highest MOx rates (7 nM d−1) in summer in bathymetric depressions filled with stagnant Atlantic Water containing moderate concentrations of dissolved CH4 (d−1) due to lower temperatures and mixing of Transformed Atlantic Water flushing MOB with the Atlantic Water out of the depressions. Our results show that MOB and MOx in CH4-rich bottom waters are highly affected by geomorphology and seasonal conditions

Compositions of dissolved organic matter in the ice-covered waters above the Aurora hydrothermal vent system, Gakkel Ridge, Arctic Ocean

Hydrothermal vents modify and displace subsurface dissolved organic matter (DOM) into the ocean. Once in the ocean, this DOM is transported together with elements, particles, dissolved gases and biomass along with the neutrally buoyant plume layer. Considering the number and extent of actively venting hydrothermal sites in the oceans, their contribution to the oceanic DOM pool may be substantial. Here, we investigate the dynamics of DOM in relation to hydrothermal venting and related processes at the as yet unexplored Aurora hydrothermal vent field within the ultraslow-spreading Gakkel Ridge in the Arctic Ocean at 82.9∘ N. We examined the vertical distribution of DOM composition from sea ice to deep waters at six hydrocast stations distal to the active vent and its neutrally buoyant plume layer. In comparison to background seawater, we found that the DOM in waters directly affected by the hydrothermal plume was molecularly less diverse and 5 %–10 % lower in number of molecular formulas associated with the molecular categories related to lipid and protein-like compounds. On the other hand, samples that were not directly affected by the plume were chemically more diverse and had a higher percentage of chemical formulas associated with the carbohydrate-like category. Our results suggest that hydrothermal processes at Aurora may influence the DOM distribution in the bathypelagic ocean by spreading more thermally and/or chemically induced compositions, while DOM compositions in epipelagic and mesopelagic layers are mainly governed by the microbial carbon pump dynamics and surface-ocean–sea-ice interactionspublishedVersio

The Postglacial response of Arctic Ocean gas hydrates to climatic amelioration

Seafloor methane release due to the thermal dissociation of gas hydrates is pervasive across the continental margins of the Arctic Ocean. Furthermore, there is increasing awareness that shallow hydrate-related methane seeps have appeared due to enhanced warming of Arctic Ocean bottom water during the last century. Although it has been argued that a gas hydrate gun could trigger abrupt climate change, the processes and rates of subsurface/atmospheric natural gas exchange remain uncertain. Here we investigate the dynamics between gas hydrate stability and environmental changes from the height of the last glaciation through to the present day. Using geophysical observations from offshore Svalbard to constrain a coupled ice sheet/gas hydrate model, we identify distinct phases of subglacial methane sequestration and subsequent release on ice sheet retreat that led to the formation of a suite of seafloor domes. Reconstructing the evolution of this dome field, we find that incursions of warm Atlantic bottom water forced rapid gas hydrate dissociation and enhanced methane emissions during the penultimate Heinrich event, the B?lling and Aller?d interstadials, and the Holocene optimum. Our results highlight the complex interplay between the cryosphere, geosphere, and atmosphere over the last 30,000 y that led to extensive changes in subseafloor carbon storage that forced distinct episodes of methane release due to natural climate variability well before recent anthropogenic warmingauthorsversionPeer reviewe

Temporal biomass dynamics of an Arctic plankton bloom in response to increasing levels of atmospheric carbon dioxide

Ocean acidification and carbonation, driven by anthropogenic emissions of carbon dioxide (CO2), have been shown to affect a variety of marine organisms and are likely to change ecosystem functioning. High latitudes, especially the Arctic, will be the first to encounter profound changes in carbonate chemistry speciation at a large scale, namely the under-saturation of surface waters with respect to aragonite, a calcium carbonate polymorph produced by several organisms in this region. During a CO2 perturbation study in Kongsfjorden on the west coast of Spitsbergen (Norway), in the framework of the EU-funded project EPOCA, the temporal dynamics of a plankton bloom was followed in nine mesocosms, manipulated for CO2 levels ranging initially from about 185 to 1420 μatm. Dissolved inorganic nutrients were added halfway through the experiment. Autotrophic biomass, as identified by chlorophyll a standing stocks (Chl a), peaked three times in all mesocosms. However, while absolute Chl a concentrations were similar in all mesocosms during the first phase of the experiment, higher autotrophic biomass was measured as high in comparison to low CO2 during the second phase, right after dissolved inorganic nutrient addition. This trend then reversed in the third phase. There were several statistically significant CO2 effects on a variety of parameters measured in certain phases, such as nutrient utilization, standing stocks of particulate organic matter, and phytoplankton species composition. Interestingly, CO2 effects developed slowly but steadily, becoming more and more statistically significant with time. The observed CO2-related shifts in nutrient flow into different phytoplankton groups (mainly dinoflagellates, prasinophytes and haptophytes) could have consequences for future organic matter flow to higher trophic levels and export production, with consequences for ecosystem productivity and atmospheric CO2.publishedVersio

Arctic Ocean carbon biogeochemistry under climate change and ocean acidification

Human-induced CO2 emissions to the atmosphere cause climate change and ocean acidification. The strongest indicators of climate change and ocean acidification are expected to be found in the Arctic Ocean (AO). The AO area is small compared to the world ocean, but the global influence of its carbon biogeochemical system with large spatial and temporal variability is considerable and complex. The AO carbon biogeochemical system is also expected to experience feedback in regard to climate change, and to influence the energy flow throughout the Arctic food web. This thesis investigates the carbon biogeochemical system in the AO: present variability; coupling with processes at the low trophic level; and response to future climate and CO2 scenarios. The study combines differing methodological approaches: (i) in-situ observations, (ii) field perturbation experiments, and (iii) ecosystem modeling. The thesis is based on four separate papers. Paper I describes the natural variability of particulate organic carbon and particulate organic nitrogen in a composition of seston and estimates the carbon to nitrogen (C:N) ratio in the AO seston. The paper is based on 3672 in-situ measurements gathered from sources both published and unpublished. The overall C:N ratio in seston was 7.4, which is significantly higher than the classical Redfield ratio of 6.6. A great regional variability in the seston C:N ratio was found. Paper II introduces the inorganic carbonate system around the Svalbard archipelago in the AO, at present and under future climate and CO2 scenarios. This paper is based on results from a coupled physical-biogeochemical ecosystem model forced by SRES A1B scenario, as well as on results of a CO2 perturbation study on the natural community conducted in an Arctic fjord. The results presented in this paper suggest that seawater pCO2 in the area around Svalbard at the end of the 21st century will be 300 μatm higher than at present in the Atlantic influenced region, and 400 μatm higher than at present in the Arctic influenced region. As a result, the waters in the Arctic-influenced region will be undersaturated with respect to aragonite, and waters in the Atlantic-influenced region will be close to the undersaturation state. The modeled summer decrease in seawater pCO2, and the increase in pH and aragonite saturation state are all steeper in the future. This was also observed during an experiment on ocean acidification in natural phytoplankton assemblage, which was perturbed with the projected high levels of seawater pCO2. Paper III is based on results from two model simulations, performed with the coupled physical-biogeochemical ecosystem model forced by SRES A1B scenario, parameterized with the constant C:N ratio and with the pCO2 sensitive C:N ratio. The paper demonstrates that more inorganic carbon could be fixed by autotrophs in the future surface Arctic waters if annual primary production increases in response to the pCO2 sensitive C:N ratio. As a result of higher primary production, and consequently higher export production in case of pCO2 sensitive C:N ratio, more carbon is released below the euphotic zone, which leads to lower pH and aragonite saturation states than in case with the constant C:N ratio. Paper IV is based on the results of the large-scale CO2 perturbation experiment, revealing enhanced carbon fixation by autotrophs at high levels of pCO2 when the phytoplankton assemblage was dominated by a smallsized phytoplankton group. The results of the paper suggest that net community production could enhance if small-sized phytoplankton thrives in the future Arctic Ocean. The introduction to the thesis provides a comprehensive overview of the carbonate system and processes controlling it. The AO carbon biogeochemistry is introduced, with its uniqueness and importance for the earth climate system. The findings of the four papers are summarized and future prospects for carbon biogeochemistry research in the AO are discussed