Interannual variability in the summer dissolved organic matter inventory of the North Sea: Implications for the continental shelf pump

We present the distribution and C:N stoichiometry of dissolved organic matter (DOM) in the North Sea in two summers (August 2011 and August 2012), with supporting data from the intervening winter (January 2012). These data demonstrate local variability superimposed on a general pattern of decreasing DOM with increasing distance from land, suggesting concentrations of DOM are controlled on large spatial scales by mixing between the open North Atlantic and either riverine sources or high DOM productivity in nearshore coastal waters driven by riverine nutrient discharge. Given the large size and long residence time of water in the North Sea, we find concentrations are commonly modified from simple conservative mixing between two endmembers. We observe differences in dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) concentrations and land-ocean gradients between the two summers, leading to an estimated 10-20Tg difference in the DOC inventory between the two years, which is of the same order of magnitude as the annual uptake of atmospheric CO 2 by the North Sea system, and thus significant for the carbon budget of the North Sea. This difference is not consistent with additional terrestrial loading and is more likely to be due to balancing of mixing and in situ production and loss processes across the North Sea. Differences were particularly pronounced in the bottom layer of the seasonally stratifying northern North Sea, with higher DOC and C:N ratio in 2011 than in 2012. Using other data, we consider the extent to which these differences in the concentrations and C:N ratio of DOM could be due to changes in the biogeochemistry or physical circulation in the two years, or a combination of both. The evidence we have is consistent with a flushing event in winter 2011/12 exchanging DOM-rich, high C:N shelf waters, which may have accumulated over more than 1 year, with deep North Atlantic waters with lower DOC and marginally higher DON. We discuss the implications of these observations for the shelf sea carbon pump and the export of carbon-rich organic matter off the shelf and hypothesise that intermittent flushing of temperate shelf systems may be a key mechanism in the maintenance of the continental shelf pump, via the accumulation and subsequent export of carbon-rich DOM

Benthic nitrogen cycling in the North Sea

We present new data on the rates of sedimentary denitrification and its component processes (canonical denitrification, anammox and dissimilatory nitrate reduction to ammonium) for intertidal and subtidal sites in the North Sea using nitrogen isotope addition methods. We find overall average denitrification rates of 6.3 (range 0.4-10.6) µmol m-2h-1, similar to those previously reported for this region and other temperate shelf environments. We find canonical denitrification to be the dominant (>90%) process of the three. At the subtidal sites, most of the denitrification is supported by nitrate generated within the sediments, while at the intertidal site the main source is from the water column. We go on to consider the impact of these rates on nitrogen cycling within the North Sea region and compare the sediment core incubation rate results to estimates derived from modelling approaches. Model rates are somewhat higher than those directly measured and we consider possible reasons for this

Estimation of the atmospheric flux of nutrients and trace metals to the Eastern Tropical North Atlantic Ocean

Atmospheric deposition contributes potentially significant amounts of the nutrients iron, nitrogen and phosphorus (via mineral dust and anthropogenic aerosols) to the oligotrophic tropical North Atlantic Ocean. Transport pathways, deposition processes and source strengths contributing to this atmospheric flux are all highly variable in space and time. Atmospheric sampling was conducted during 28 research cruises through the Eastern Tropical North Atlantic (ETNA) over a 12 year period and a substantial dataset of measured concentrations of nutrients and trace metals in aerosol and rainfall over the region was acquired. This database was used to quantify (on a spatial- and seasonal-basis) the atmospheric input of ammonium, nitrate, soluble phosphorus and soluble and total iron, aluminium and manganese to the ETNA. The magnitude of atmospheric input varies strongly across the region, with high rainfall rates associated with the Inter-tropical Convergence Zone contributing to high wet deposition fluxes in the south, particularly for soluble species. Dry deposition fluxes of species associated with mineral dust exhibited strong seasonality, with highest fluxes associated with winter-time low-level transport of Saharan dust. Overall (wet plus dry) atmospheric inputs of soluble and total trace metals were used to estimate their soluble fractions. These also varied with season and were generally lower in the dry north than in the wet south. The ratio of ammonium plus nitrate to soluble iron in deposition to the ETNA was lower than the N:Fe requirement for algal growth in all cases, indicating the importance of the atmosphere as a source of excess iron

Western Pacific atmospheric nutrient deposition fluxes, their impact on surface ocean productivity

The atmospheric deposition of both macronutrients and micronutrients plays an important role in driving primary productivity, particularly in the low-latitude ocean. We report aerosol major ion measurements for five ship-based sampling campaigns in the western Pacific from similar to 25 degrees N to 20 degrees S and compare the results with those from Atlantic meridional transects (similar to 50 degrees N to 50 degrees S) with aerosols collected and analyzed in the same laboratory, allowing full incomparability. We discuss sources of the main nutrient species (nitrogen (N), phosphorus (P), and iron (Fe)) in the aerosols and their stoichiometry. Striking north-south gradients are evident over both basins with the Northern Hemisphere more impacted by terrestrial dust sources and anthropogenic emissions and the North Atlantic apparently more impacted than the North Pacific. We estimate the atmospheric supply rates of these nutrients and the potential impact of the atmospheric deposition on the tropical western Pacific. Our results suggest that the atmospheric deposition is P deficient relative to the needs of the resident phytoplankton. These findings suggest that atmospheric supply of N, Fe, and P increases primary productivity utilizing some of the residual excess phosphorus (P*) in the surface waters to compensate for aerosol P deficiency. Regional primary productivity is further enhanced via the stimulation of nitrogen fixation fuelled by the residual atmospheric iron and P*. Our stoichiometric calculations reveal that a P* of 0.1 mu mol L-1 can offset the P deficiency in atmospheric supply for many months. This study suggests that atmospheric deposition may sustain similar to 10% of primary production in both the western tropical Pacific

Iron biogeochemistry across marine systems progress from the past decade

Based on an international workshop (Gothenburg, 14–16 May 2008), this review article aims to combine interdisciplinary knowledge from coastal and open ocean research on iron biogeochemistry. The major scientific findings of the past decade are structured into sections on natural and artificial iron fertilization, iron inputs into coastal and estuarine systems, colloidal iron and organic matter, and biological processes. Potential effects of global climate change, particularly ocean acidification, on iron biogeochemistry are discussed. The findings are synthesized into recommendations for future research areas

Seasonal ITCZ migration dynamically controls the location of the (sub)tropical Atlantic biogeochemical divide

Inorganic nitrogen depletion restricts productivity in much of the low-latitude oceans, generating a selective advantage for diazotrophic organisms capable of fixing atmospheric dinitrogen (N2). However, the abundance and activity of diazotrophs can in turn be controlled by the availability of other potentially limiting nutrients, including phosphorus (P) and iron (Fe). Here we present high-resolution data (∼0.3°) for dissolved iron, aluminum, and inorganic phosphorus that confirm the existence of a sharp north–south biogeochemical boundary in the surface nutrient concentrations of the (sub)tropical Atlantic Ocean. Combining satellite-based precipitation data with results from a previous study, we here demonstrate that wet deposition in the region of the intertropical convergence zone acts as the major dissolved iron source to surface waters. Moreover, corresponding observations of N2 fixation and the distribution of diazotrophic Trichodesmium spp. indicate that movement in the region of elevated dissolved iron as a result of the seasonal migration of the intertropical convergence zone drives a shift in the latitudinal distribution of diazotrophy and corresponding dissolved inorganic phosphorus depletion. These conclusions are consistent with the results of an idealized numerical model of the system. The boundary between the distinct biogeochemical systems of the (sub)tropical Atlantic thus appears to be defined by the diazotrophic response to spatial–temporal variability in external Fe inputs. Consequently, in addition to demonstrating a unique seasonal cycle forced by atmospheric nutrient inputs, we suggest that the underlying biogeochemical mechanisms would likely characterize the response of oligotrophic systems to altered environmental forcing over longer timescales

Quantifying and valuing carbon flows and stores in coastal and shelf ecosystems in the UK

Evidence shows that habitats with potential to mitigate against greenhouse gases emissions, by taking up and storing CO2, are being lost due to the effects of on-going human activities and climate change. The carbon storage by terrestrial habitats (e.g. tropical forests) and the role of coastal habitats (‘Blue Carbon’) as carbon storage sinks is well recognised. Offshore shelf sediments are also a manageable carbon store, covering ∼9% of global marine area, but not currently protected by international agreements to enable their conservation. Through a scenario analysis, we explore the economic value of the damage of human activities and climate change can inflict on UK marine habitats, including shelf sea sediments. In a scenario of increased human and climate pressures over a 25-year period, we estimate damage costs up to US$12.5 billion from carbon release linked to disturbance of coastal and shelf sea sediment carbon stores. It may be possible to manage socio-economic pressure to maintain sedimentary carbon storage, but the trade-offs with other global social welfare benefits such as food security will have to be taken into account. To develop effective incentive mechanisms to preserve these valuable coastal and marine ecosystems within a sustainability governance framework, robust evidence is required

Governing processes for reactive nitrogen compounds in the atmosphere in relation to ecosystem climatic and human health impacts

Reactive nitrogen (Nr) compounds have different fates in the atmosphere due to differences in governing processes of physical transport, deposition and chemical transformation. Nr compounds addressed here include reduced nitrogen (NHx: ammonia (NH3) and its reaction product ammonium (NH4+)), oxidized nitrogen (NOy: nitrogen monoxide (NO) + nitrogen dioxide (NO2) and their reaction products) as well as organic nitrogen compounds (organic N). Pollution abatement strategies need to take into account these differences in the governing processes of these compounds when assessing their impact on ecosystem services, biodiversity, human health and climate. NOx (NO + NO2) emitted from traffic affects human health in urban areas where the presence of buildings increases the residence time in streets. In urban areas this leads to enhanced exposure of the population to NOx concentrations. NOx emissions have little impact on nearby ecosystems because of the small dry deposition rates of NOx. These compounds need to be converted into nitric acid (HNO3) before removal through deposition is efficient. HNO3 sticks quickly to any surface and is thereby either dry deposited or incorporated into aerosols as nitrate (NO3−). In contrast to NOx compounds, NH3 has potentially high impacts on ecosystems near the main agricultural sources of NH3 because of its large ground-level concentrations along with large dry deposition rates. Aerosol phase NH4+ and NO3− contribute significantly to background PM2.5 and PM10 (mass of aerosols with a diameter of less than 2.5 and 10 μm, respectively) with an impact on radiation balance as well as potentially on human health. Little is known quantitatively and qualitatively about organic N in the atmosphere, other than that it contributes a significant fraction of wet-deposited N, and is present in both gaseous and particulate forms in the atmosphere. Further studies are needed to characterize the sources, air chemistry and removal rates of organic N emissions