Description: The effect of CO2 on carbon fluxes in Arctic plankton communities was investigated during the 2010 EPOCA mesocosm study in Ny Ålesund, Svalbard. Nine mesocosms were set up with initial pCO2 levels ranging from 185 to 1420 μatm for 5 weeks. 13C labelled bicarbonate was added at the start of the experiment to follow the transfer of carbon from dissolved inorganic carbon (DIC) into phytoplankton, bacteria, total particulate organic carbon (POC), zooplankton, and settling particles. Polar lipid derived fatty acids (PLFA) were used to trace carbon dynamics of phytoplankton and bacteria and allowed distinction of two groups of phytoplankton: phyto I (autotrophs) and phyto II (mixotrophs). Nutrients were added on day 13. A nutrient-phytoplankton-zooplankton-detritus model amended with 13C dynamics was constructed and fitted to the data to quantify uptake rates and carbon fluxes in the plankton community during the phase prior to nutrient addition (phase 1, days 0–12). During the first 12 days, a phytoplankton bloom developed that was characterized by high growth rates (0.87 days−1) for phyto I and lower growth rates (0.18 days−1) for phyto II. A large part of the carbon fixed by phytoplankton (~31%) was transferred to bacteria, while mesozooplankton grazed only ~6% of the production. After 6 days, the bloom collapsed and part of the organic matter subsequently settled into the sediment traps. The sedimentation losses of detritus in phase 1 were low (0.008 days−1) and overall export was only ~7% of production. Zooplankton grazing and detritus sinking losses prior to nutrient addition were sensitive to CO2: grazing decreased with increasing CO2, while sinking increased. Phytoplankton production increased again after nutrient addition on day 13. Although phyto II showed initially higher growth rates with increasing CO2 (days 14–22), the overall production of POC after nutrient addition (phase 2, days 14–29) decreased with increasing CO2. Significant sedimentation occurred towards the end of the experiment (after day 24) and much more material settled down in the sediment traps at low CO2.

Description: The ocean's nitrogen cycle is driven by complex microbial transformations, including nitrogen fixation, assimilation, nitrification, anammox and denitrification. Dinitrogen is the most abundant form of nitrogen in sea water but only accessible by nitrogen-fixing microbes. Denitrification and nitrification are both regulated by oxygen concentrations and potentially produce nitrous oxide (N2O), a climate-relevant atmospheric trace gas. The world's oceans, including the coastal areas and upwelling areas, contribute about 30 per cent to the atmospheric N2O budget and are, therefore, a major source of this gas to the atmosphere. Human activities now add more nitrogen to the environment than is naturally fixed. More than half of the nitrogen reaches the coastal ocean via river input and atmospheric deposition, of which the latter affects even remote oceanic regions. A nitrogen budget for the coastal and open ocean, where inputs and outputs match rather well, is presented. Furthermore, predicted climate change will impact the expansion of the oceans' oxygen minimum zones, the productivity of surface waters and presumably other microbial processes, with unpredictable consequences for the cycling of nitrogen. Nitrogen cycling is closely intertwined with that of carbon, phosphorous and other biologically important elements via biological stoichiometric requirements. This linkage implies that human alterations of nitrogen cycling are likely to have major consequences for other biogeochemical processes and ecosystem functions and services.

Description: The benthic diagenetic model OMEXDIA has been used to reproduce observed benthic pore water and solid phase profiles obtained during the OMEX study in the Goban Spur Area (N.E. Atlantic), and to dynamically model benthic profiles at site OMEX III (3660-m depth), with the sediment trap organic flux as external forcing. The results of the dynamic modelling show that the organic flux as determined from the lowermost sediment trap (400 metres above the bottom) at OMEX III is insufficient to explain the organic carbon and pore water profiles. The best fitting was obtained by maintaining the seasonal pattern as observed in the traps, while multiplying the absolute values of the flux by a factor of 1.85. The “inverse modelling” of diagenetic processes resulted in estimates of total mineralisation rate and of degradability of the organic matter at the different stations. These diagenetic model-based estimates are used to constrain the patterns of lateral and vertical transports of organic matter. Using the observed degradability as a function of depth, we show that the observed organic matter fluxes at the different depths are consistent with a model where at all stations along the gradient the same vertical export flux occurs at 200 m, and where organic matter sinks with a constant sinking rate of around 130 m d−1. If sinking rates were higher, in the order of 200 m d−1, the observations could be consistent with an off-slope gradient in export production of approximately a factor of 1.5 between the shallowest and deepest sites. The derived high degradability of the arriving organic matter and the consistency of the mass fluxes at the different stations exclude the possibility of a massive deposition, on the margin, of organic matter produced on the shelf or shelf break. However, other hypotheses to explain the patterns found in the sediment trap data of both OMEX and other continental margin study sites also suffer from different inconsistencies. Further, close examination of the flow patterns at the margin will be needed to examine the question.

Description: We report a new synthesis of best estimates of the inputs of fixed nitrogen to the world ocean via atmospheric deposition and compare this to fluvial inputs and dinitrogen fixation. We evaluate the scale of human perturbation of these fluxes. Fluvial inputs dominate inputs to the continental shelf, and we estimate that about 75% of this fluvial nitrogen escapes from the shelf to the open ocean. Biological dinitrogen fixation is the main external source of nitrogen to the open ocean, i.e., beyond the continental shelf. Atmospheric deposition is the primary mechanism by which land-based nitrogen inputs, and hence human perturbations of the nitrogen cycle, reach the open ocean. We estimate that anthropogenic inputs are currently leading to an increase in overall ocean carbon sequestration of ~0.4% (equivalent to an uptake of 0.15 Pg C yr−1 and less than the Duce et al. (2008) estimate). The resulting reduction in climate change forcing from this ocean CO2 uptake is offset to a small extent by an increase in ocean N2O emissions. We identify four important feedbacks in the ocean atmosphere nitrogen system that need to be better quantified to improve our understanding of the perturbation of ocean biogeochemistry by atmospheric nitrogen inputs. These feedbacks are recycling of (1) ammonia and (2) organic nitrogen from the ocean to the atmosphere and back, (3) the suppression of nitrogen fixation by increased nitrogen concentrations in surface waters from atmospheric deposition, and (4) increased loss of nitrogen from the ocean by denitrification due to increased productivity stimulated by atmospheric inputs.

Description: The potential impact of rising carbon dioxide (CO2) on carbon transfer from phytoplankton to bacteria was investigated during the 2005 PeECE III mesocosm study in Bergen, Norway. Sets of mesocosms, in which a phytoplankton bloom was induced by nutrient addition, were incubated under 1× (~350 μatm), 2× (~700 μatm), and 3× present day CO2 (~1050 μatm) initial seawater and sustained atmospheric CO2 levels for 3 weeks. 13C labelled bicarbonate was added to all mesocosms to follow the transfer of carbon from dissolved inorganic carbon (DIC) into phytoplankton and subsequently heterotrophic bacteria, and settling particles. Isotope ratios of polar-lipid-derived fatty acids (PLFA) were used to infer the biomass and production of phytoplankton and bacteria. Phytoplankton PLFA were enriched within one day after label addition, whilst it took another 3 days before bacteria showed substantial enrichment. Group-specific primary production measurements revealed that coccolithophores showed higher primary production than green algae and diatoms. Elevated CO2 had a significant positive effect on post-bloom biomass of green algae, diatoms, and bacteria. A simple model based on measured isotope ratios of phytoplankton and bacteria revealed that CO2 had no significant effect on the carbon transfer efficiency from phytoplankton to bacteria during the bloom. There was no indication of CO2 effects on enhanced settling based on isotope mixing models during the phytoplankton bloom, but this could not be determined in the post-bloom phase. Our results suggest that CO2 effects are most pronounced in the post-bloom phase, under nutrient limitation.

Description: The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean acidification on marine organisms and communities but few have provided details concerning full carbonate chemistry and complementary observations. Additionally, carbonate system variables are often reported in different units, calculated using different sets of dissociation constants and on different pH scales. Hence the direct comparison of experimental results has been problematic and often misleading. The need was identified to (1) gather data on carbonate chemistry, biological and biogeochemical properties, and other ancillary data from published experimental data, (2) transform the information into common framework, and (3) make data freely available. The present paper is the outcome of an effort to integrate ocean carbonate chemistry data from the literature which has been supported by the European Network of Excellence for Ocean Ecosystems Analysis (EUR-OCEANS) and the European Project on Ocean Acidification (EPOCA). A total of 185 papers were identified, 100 contained enough information to readily compute carbonate chemistry variables, and 81 data sets were archived at PANGAEA – The Publishing Network for Geoscientific & Environmental Data. This data compilation is regularly updated as an ongoing mission of EPOCA.

Description: We provide an overview of the role of biological processes in the Benthic boundary layer (BBL) and in sediments on the cycling of particulate organic material in the Goban Spur area (Northeast Atlantic). The benthic fauna, sediment and BBL characteristics were studied along a transect ranging from 208 to 4460 m water depth in different seasons over 3 years. Near-bottom flow velocities are high at the upper part of the slope (1000–1500 m), and high numbers of filter-feeding taxa are found there such that organic carbon normally passing this area during high flow conditions is probably trapped, accumulated, and/or remineralised by the fauna. Overall metabolism in shelf and upper slope sediments is dominated by the macrofauna. More than half of the organic matter flux is respired by macrofauna, with a lower contribution of metazoan meiofauna (4%) and anoxic and suboxic bacterial mineralisation (21%); the remainder (23%) being channelled through nanobiota and oxic bacteria. By its feeding activity and movement, the macrofauna intensely reworks the sediments on the shelf and upper slope. Mixing intensity of bulk sediment and of organic matter are of comparable magnitude. The benthos of the lower slope and abyssal depth is dominated by the microbiota, both in terms of total biomass (〉90%) and carbon respiration (about 80%). The macrofauna (16%), meiofauna (4%) and megafauna (0.5%) only marginally contribute to total carbon respiration at depths below 1400 m. Because large animals have a lower share in total metabolism, mixing of organic matter within the sediments is reduced by a factor of 5, whereas mixing of bulk sediment is one to two orders of magnitude lower than on the shelf. The food quality of organic matter in the sediments in the shallowest part of the Goban Spur transect is significantly higher than in sediments in the deeper parts. The residence time of mineralisable carbon is about 120 d on the shelf and compares well with the residence time of the biota. In the deepest station, the mean residence time of mineralisable carbon is more than 3000 d, an order of magnitude higher than that of biotic biomass.