Description: The Joint Global Ocean Flux Study (JGOFS) has completed a decade of intensive process and time-series studies on the regional and temporal dynamics of biogeochemical processes in five diverse ocean basins. Its field program also included a global survey of dissolved inorganic carbon (DIC) in the ocean, including estimates of the exchange of carbon dioxide (CO2) between the ocean and the atmosphere, in cooperation with the World Ocean Circulation Experiment (WOCE). This report describes the principal achievements of JGOFS in ocean observations, technology development and modelling. The study has produced a comprehensive and high-quality database of measurements of ocean biogeochemical properties. Data on temporal and spatial changes in primary production and CO2 exchange, the dynamics of of marine food webs, and the availability of micronutrients have yielded new insights into what governs ocean productivity, carbon cycling and export into the deep ocean, the set of processes collectively known as the "biological pump." With large-scale, high-quality data sets for the partial pressure of CO2 in surface waters as well for other DIC parameters in the ocean and trace gases in the atmosphere, reliable estimates, maps and simulations of air-sea gas flux, anthropogenic carbon and inorganic carbon export are now available. JGOFS scientists have also obtained new insights into the export flux of particulate and dissolved organic carbon (POC and DOG), the variations that occur in the ratio of elements in organic matter, and the utilization and remineralization of organic matter as it falls through the ocean interior to the sediments. JGOFS scientists have amassed long-term data on temporal variability in the exchange of CO2 between the ocean and atmosphere, ecosystem dynamics, and carbon export in the oligotrophic subtropical gyres. They have documented strong links between these variables and large-scale climate patterns such as the El Nino-Southern Oscillation (ENSO) or the North Atlantic Oscillation (NAO). An increase in the abundance of organisms that fix free nitrogen (N-2) and a shift in nutrient limitation from nitrogen to phosphorus in the subtropical North Pacific provide evidence of the effects of a decade of strong El Ninos on ecosystem structure and nutrient dynamics. High-quality data sets, including ocean-color observations from satellites, have helped modellers make great strides in their ability to simulate the biogeochemical and physical constraints on the ocean carbon cycle and to extend their results from the local to the regional and global scales. Ocean carbon-cycle models, when coupled to atmospheric and terrestrial models, will make it possible in the future to predict ways in which land and ocean ecosystems might respond to changes in climate.

Description: Measurements of near-surface oxygen (O2) concentrations and mixed layer depth from the K1 mooring in the central Labrador Sea are used to calculate the change in column-integrated (0–1700 m) O2 content over the deep convection winter 2014/2015. During the mixed layer deepening period, November 2014 to April 2015, the oxygen content increased by 24.3 ± 3.4 mol m−2, 40% higher than previous results from winters with weaker convection. By estimating the contribution of respiration and lateral transport on the oxygen budget, the cumulative air-sea gas exchange is derived. The O2 uptake of 29.1 ± 3.8 mol m−2, driven by persistent undersaturation (≥5%) and strong atmospheric forcing, is substantially higher than predicted by standard (nonbubble) gas exchange parameterizations, whereas most bubble-resolving parameterizations predict higher uptake, comparable to our results. Generally large but varying mixed layer depths and strong heat and momentum fluxes make the Labrador Sea an ideal test bed for process studies aimed at improving gas exchange parameterizations.

Description: We use isoprene and related field measurements from three different ocean data sets together with remotely sensed satellite data to model global marine isoprene emissions. We show that using monthly mean satellite-derived chl a concentrations to parameterize isoprene with a constant chl a normalized isoprene production rate underpredicts the measured oceanic isoprene concentration by a mean factor of 19 ± 12. Improving the model by using phytoplankton functional type dependent production values and by decreasing the bacterial degradation rate of isoprene in the water column results in only a slight underestimation (factor 1.7 ± 1.2). We calculate global isoprene emissions of 0.21 Tg C for 2014 using this improved model, which is twice the value calculated using the original model. Nonetheless, the sea-to-air fluxes have to be at least 1 order of magnitude higher to account for measured atmospheric isoprene mixing ratios. These findings suggest that there is at least one missing oceanic source of isoprene and, possibly, other unknown factors in the ocean or atmosphere influencing the atmospheric values. The discrepancy between calculated fluxes and atmospheric observations must be reconciled in order to fully understand the importance of marine-derived isoprene as a precursor to remote marine boundary layer particle formation.

Description: From October 2008 to November 2010, CH3I concentrations were measured in the Kiel Fjord together with potentially related biogeochemical and physical parameters. A repeating seasonal cycle of CH3I was observed with highest concentrations in summer (ca. 8.3 pmol L−1; June and July) and lowest concentrations in winter (ca. 1.5 pmol L−1; December to February). A strong positive correlation at zero lag between [CH3I] and solar radiation (R2 = 0.93) was observed, whereas correlations with other variables (SST, Chlorophyll a) were weaker, and they lagged CH3I by ca. 1 month. These results appear consistent with the hypothesis that SSR is the primary forcing of CH3I production in surface seawater, possibly through a photochemical pathway. A mass balance of the monthly averaged data was used to infer mean rates of daily net production (Pnet) and losses for CH3I over the year. The sea-to-air flux of CH3I in the Kiel Fjord averaged 3.1 nmol m−2 d−1, the mean chemical loss rate was 0.047 pmol L−1 d−1, and Pnet varied systematically from winter to summer (from 0 to 0.6 pmol L−1 d−1). Pnet was correlated at zero lag with SST, SSR, and Chla (R2 = 0.55, 0.67, and 0.73, respectively, p 〈〈 0.01). The lagged cross-correlation analysis indicated that SSR led Pnet by 1 month, whereas the strongest cross correlations with Chla were at lags of 0 to +1 month, and SST lagged Pnet by 1 month. The broad seasonal peak of Pnet makes it difficult to determine the key factor controlling CH3I net production using in situ concentration data alone.

Description: Here we present first observations, from instrumentation installed on moorings and a float, of unexpectedly low (〈2 μmol kg−1) oxygen environments in the open waters of the tropical North Atlantic, a region where oxygen concentration does normally not fall much below 40 μmol kg−1. The low-oxygen zones are created at shallow depth, just below the mixed layer, in the euphotic zone of cyclonic eddies and anticyclonic-modewater eddies. Both types of eddies are prone to high surface productivity. Net respiration rates for the eddies are found to be 3 to 5 times higher when compared with surrounding waters. Oxygen is lowest in the centre of the eddies, in a depth range where the swirl velocity, defining the transition between eddy and surroundings, has its maximum. It is assumed that the strong velocity at the outer rim of the eddies hampers the transport of properties across the eddies boundary and as such isolates their cores. This is supported by a remarkably stable hydrographic structure of the eddies core over periods of several months. The eddies propagate westward, at about 4 to 5 km day−1, from their generation region off the West African coast into the open ocean. High productivity and accompanying respiration, paired with sluggish exchange across the eddy boundary, create the "dead zone" inside the eddies, so far only reported for coastal areas or lakes. We observe a direct impact of the open ocean dead zones on the marine ecosystem as such that the diurnal vertical migration of zooplankton is suppressed inside the eddies.

Description: The transit time distribution method was applied to dichlorodifluoromethane and sulfur hexafluoride measurements from four cruises to the tropical North Atlantic between 2006 and 2009 in order to estimate anthropogenic carbon (C-ant) concentrations. By assuming an Inverse Gaussian distribution of the transit time distribution the best fit to the data was achieved with the ratio of mean age to width equals 1. Significant differences in the mean age and C-ant concentrations between the equatorial belt (5 degrees S-5 degrees N) and the Guinea dome area (5 degrees-15 degrees N) was found. Mean ages are higher and C-ant concentrations are lower in the Guinea dome area than at same depths, or densities, in the equatorial belt. The mean column inventories in the upper 1200 m are higher by about 3 mol m(-2) in the equatorial belt compared to the Guinea dome area. The mean column inventory of C-ant, for the whole water column, in the tropical Atlantic is 32.2 mol m(-2) (error range: 30.6-45.2 mol m(-2)), which is significantly lower than the previous estimates. The total C-ant inventory in the eastern tropical Atlantic is 2.5 Pg (error range: 2.3-3.5 Pg) for an area of 6 x 10(6) km(2), comprising the Guinea dome region and the equatorial belt. The equatorial belt has 40% higher storage of C-ant compared to the Guinea dome area which reflects the occurrence of relatively young deep waters at the equator, being high in anthropogenic carbon. Our tracer based C-ant estimates were compared to C-ant concentrations calculated with the TrOCA method applied to measurements conducted in 1999. The TrOCA based estimates are significantly higher than our tracer based C-ant estimates. Comparison between tracer measurements in 1999 and the 2006-2009 time-frame revealed possible speed-up of ventilation in the upper water column, increasing the C-ant concentration in this depth range at a faster rate and a C-ant increase of 12.1 mu mol kg(-1) in the tropical surface water was found

Description: A deliberate tracer release experiment in 2008–2010 was used to study diapycnal mixing in the tropical northeastern Atlantic. The tracer (CF3SF5) was injected on the isopycnal surface σΘ = 26.88 kg m−3, which corresponds to about 330 m depth. Three surveys, performed 7, 20, and 30 months after the release, sampled the vertically and laterally expanding tracer patch. The mean diapycnal mixing estimate over the entire region occupied by the tracer and the period of 30 months was found to be (1.19 ± 0.18) × 10−5 m2 s−1, or, alternatively, (3.07 ± 0.58) × 10−11 (kg m−3)2 s−1 as computed from the advection-diffusion equation in isopycnal coordinates with the thickness-weighted averaging. The latter method is preferable in the regions of different stratification for it yields local diapycnal mixing estimates varying less with stratification than their Cartesian coordinate counterparts. Results of this study are comparable to the results of the North Atlantic tracer release experiment (NATRE). However, the internal wave-wave interaction models predict reduced mixing from the breaking of internal waves at low latitudes. Thus, the diapycnal diffusivity found in this study is higher than parameterized by the low latitude of the site (4°N–12°N).

Description: Fixed nitrogen (N) loss to biogenic N2 in intense oceanic O2 minimum zones (OMZ) accounts for a large fraction of the global N sink and is an essential control on the ocean's N budget. However, major uncertainties exist regarding microbial pathways as well as net impact on the magnitude of N-loss and the ocean's overall N budget. Here we report the discovery of a N-loss hotspot in the Peru OMZ associated with a coastally trapped mesoscale eddy that is marked by an extreme N deficit matched by biogenic N2 production, high NO2− levels, and the highest isotope enrichments observed so far in OMZ's for the residual NO3−. High sea surface chlorophyll (SSC) in seaward flowing streamers provides evidence for offshore eddy transport of highly productive, inshore water. Resulting pulses in the downward flux of particles likely stimulated heterotrophic dissimilatory NO3− reduction and subsequent production of biogenic N2. The associated temporal/spatial heterogeneity of N-loss, mediated by a local succession of microbial processes, may explain inconsistencies observed among prior studies. Similar transient enhancements of N-loss likely occur within all other major OMZ's exerting a major influence on global ocean N and N isotope budgets.

Description: Dangerous climate change is best avoided by drastically and rapidly reducing greenhouse gas emissions. Nevertheless, geoengineering options are receiving attention on the basis that additional approaches may also be necessary. Here we review the state of knowledge on large-scale ocean fertilization by adding iron or other nutrients, either from external sources or via enhanced ocean mixing. On the basis of small-scale field experiments carried out to date and associated modelling, the maximum benefits of ocean fertilization as a negative emissions technique are likely to be modest in relation to anthropogenic climate forcing. Furthermore, it would be extremely challenging to quantify with acceptable accuracy the carbon removed from circulation on a long term basis, and to adequately monitor unintended impacts over large space and time-scales. These and other technical issues are particularly problematic for the region with greatest theoretical potential for the application of ocean fertilization, the Southern Ocean. Arrangements for the international governance of further field-based research on ocean fertilization are currently being developed, primarily under the London Convention/London Protocol. Highlights: ► Fertilization using iron can increase the uptake of CO2 across the sea surface. ► But most of this uptake is transient; long-term sequestration is difficult to assess. ► Unintended impacts of ocean fertilization may be far removed in space and time. ► For climate benefits, the Southern Ocean has most potential – also most problems. ► A regulatory framework for ocean fertilization research has been developed.

Description: Methyl iodide (CH3I}, bromoform (CHBr3) and dibromomethane (CH2Br2), which are produced naturally in the oceans, take part in ozone chemistry both in the troposphere and the stratosphere. The significance of oceanic upwelling regions for emissions of these trace gases in the global context is still uncertain although they have been identified as important source regions. To better quantify the role of upwelling areas in current and future climate, this paper analyzes major factors that influenced halocarbon emissions from the tropical North East Atlantic including the Mauritanian upwelling during the DRIVE expedition. Diel and regional variability of oceanic and atmospheric CH3I, CHBr3 and CH2Br2 was determined along with biological and meteorological parameters at six 24 h-stations. Low oceanic concentrations of CH3I from 0.1–5.4 pmol L-1 were equally distributed throughout the investigation area. CHBr3 of 1.0–42.4 pmol L-1 and CH2Br2 of 1.0–9.4 pmol L-1 were measured with maximum concentrations close to the Mauritanian coast. Atmospheric mixing rations of CH3I of up to 3.3, CHBr3 to 8.9 and CH2Br2 to 3.1 ppt above the upwelling and 1.8, 12.8, respectively 2.2 ppt at a Cape Verdean coast were detected during the campaign. While diel variability in CH3I emissions could be mainly ascribed to oceanic non-biological production, no main driver was identified for its emissions in the entire study region. In contrast, oceanic bromocarbons resulted from biogenic sources which were identified as regional drivers of their sea-to-air fluxes. The diel impact of wind speed on bromocarbon emissions increased with decreasing distance to the coast. The height of the marine atmospheric boundary layer (MABL) was determined as an additional factor influencing halocarbon emissions. Oceanic and atmospheric halocarbons correlated well in the study region and in combination with high oceanic CH3I, CHBr3 and CH2Br2 concentrations, local hot spots of atmospheric halocarbons could solely be explained by marine sources. This conclusion is in contrast with previous studies that hypothesized the occurrence of elevated atmospheric halocarbons over the eastern tropical Atlantic mainly originating from the West-African continent.