Dissolved organic carbon and apparent oxygen utilization in the Atlantic Ocean

Dissolved organic carbon (DOC) distributions along two Atlantic Meridional Transects conducted in 2005 in the region between 47°N and 34°S showed clear latitudinal patterns. The DOC concentrations in the epipelagic zone (0–100 m) were the highest (70–90 µM) in tropical and subtropical waters with stable mixed layers, and lowest (50–55 µM) at the poleward extremities of the transects due to deep convective mixing supplying low DOC waters to the surface. A decrease in DOC occurred with depth, and lowest DOC concentrations (41–45 µM) in the 100–300 m depth range were observed in the equatorial region due to upwelling of low DOC waters. A strong relationship between DOC and AOU was observed in the σ–t 26–26.5 isopycnal layer which underlies the euphotic zone and outcrops at the poleward extremities of the North and South Atlantic Subtropical Gyres (NASG and SASG) in the region ventilating the thermocline waters. Our observations reveal significant north–south variability in the DOC–AOU relationship. The gradient of the relationship suggests that 52% of the AOU in the σ–t 26–26.5 density range was driven by DOC degradation in the NASG and 36% in the SASG, with the remainder due to the remineralisation of sinking particulate material. We assess possible causes for the greater contribution of DOC remineralisation in the NASG compared to the SASG.     

Seasonal and spatial variability in N2O distribution in the Arabian Sea

Extensive measurements of nitrous oxide (N₂O) were made in the central and eastern Arabian Sea during the northeast monsoon (February–March), intermonsoon (April–May) and southwest monsoon (July–August) seasons. The latitudinal and longitudinal variations, along with seasonal changes with respect to winter convection and coastal upwelling, are clearly discernible. Vertical profiles collected down to 1000 m show that the Arabian Sea water column is supersaturated with N₂O at all depths. However, N₂O consumption at intermediate depths, coincident with the oxygen minimum and associated with sediment–water interfaces, and in the denitrifying zone, coincident with NO^-₂ secondary maxima, are also apparent. The N₂O concentration varies from ∼10 nM near the surface to about 80 nM in the secondary peak region (≈800 m). Interrelationships with chemical parameters suggest nitrification to be the main process for the production of N₂O in the oceanic water. Plots of apparent oxygen utilization vs production of N₂O indicate a consistent linear relationship for AOU between 0 and 200 μM.     

Total organic and inorganic carbon exchange through the Strait of Gibraltar in September 1997

The total organic carbon (TOC) and total inorganic carbon (C_T) exchange between the Atlantic Ocean and the Mediterranean Sea was studied in the Strait of Gibraltar in September 1997. Samples were taken at eight stations from western and eastern entrances of the Strait and at the middle of the Strait (Tarifa Narrows). TOC was analyzed by a high-temperature catalytic oxidation method, and C_T was calculated from alkalinity–pH_T pairs and appropriate thermodynamic relationships. The results are used in a two-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, the Mediterranean outflow and the interface layer in between. Our observations show a decrease of TOC and an increase of C_T concentrations from the surface to the bottom: 71–132 μM C and 2068–2150 μmol kg⁻¹ in the Surface Atlantic Water, 74–95 μM C and 2119–2148 μmol kg⁻¹ in the North Atlantic Central Water, 63–116 μM C and 2123–2312 μmol kg⁻¹ in the interface layer, and 61–78 μM C and 2307–2325 μmol kg⁻¹ in the Mediterranean waters. However, within the Mediterranean outflow, we found that the concentrations of carbon were higher at the western side of the Strait (75–78 μM C, 2068–2318 μmol kg⁻¹) than at the eastern side (61–69 μM C, 2082–2324 μmol kg⁻¹). This difference is due to the mixing between the Atlantic inflow and the Mediterranean outflow on the west of the Strait, which results in a flux of organic carbon from the inflow to the outflow and an opposite flux of inorganic carbon. We estimate that the TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from (0.97±0.8)10⁴ to (1.81±0.90)10⁴ mol C s⁻¹ (0.3×10¹² to 0.56×10¹² mol C yr⁻¹), while outflow of inorganic carbon ranges from (12.5±0.4)10⁴ to (15.6±0.4)10⁴ mol C s⁻¹ (3.99–4.90×10¹² mol C yr⁻¹). The high variability of carbon exchange within the Strait is due to the variability of vertical mixing between inflow and outflow along the Strait. The prevalence of organic carbon inflow and inorganic carbon outflow shows the Mediterranean Sea to be a basin of active remineralization of organic material.     

Dissolved and particulate organic carbon and nitrogen in the Northwestern Mediterranean

The distribution of dissolved organic carbon (DOC) and nitrogen (DON) and particulate organic carbon (POC) and nitrogen (PON) was studied on a transect perpendicular to the Catalan coast in the NW Mediterranean in June 1995. The transect covered a hydrographically diverse zone, including coastal waters and two frontal structures (the Catalan and the Balear fronts). The cruise was conducted during the stratified period, characterized by inorganic nutrient depletion in the photic zone and a well established deep chlorophyll a maximum. DOC concentrations were measured using a high-temperature catalytic oxidation method, and DON was determined directly, with an update of the Kjeldahl method, after removal of inorganic nitrogen.The ranges of DOC and DON concentrations were 44–95 μM-C and 2.8–6.2 μM-N. The particulate organic matter ranged between 0.9 and 14.9 μM-C and from 0.1 to 1.7 μM-N. The DOC : DON molar ratio averaged 15.5±0.4, and the mean POC : PON ratio was 8.6±0.6. The distribution of dissolved organic matter (DOM) was inverse to that of the salinity. The highest concentrations of DOM were found in coastal waters and in the stations affected by the Catalan front, located at the continental shelf break.It was estimated that recalcitrant DOM constituted 67% of the DOM pool in the upper 50 m. The data suggest that accumulation of DOC due to the decoupling of production and consumption may occur in the NW Mediterranean during stratification and that the organic matter exported from the photic layer is dominated by C-rich material.     

Vertical distributions of dissolved organic carbon and nitrogen in the Southern Ocean

Detailed vertical profiles of dissolved organic carbon (DOC), nitrogen (DON) and DOC/DON ratios in the Australian sector of the Southern Ocean (56°–65°S around 140°W transect) were obtained by a high-temperature catalytic oxidation method with a modified Shimadzu TOC-5000 unit. The simultaneous analyses of DOC and total dissolved nitrogen (TDN) gave high precision results (±0.7 μMC and ±0.3 μMN). In surface layers, DOC concentrations were lower (45–55 μM) than those generally obtained from other oceanic environments (60–90 μM). The surface concentrations of DON varied from 4 to 9 μM, but within the range generally reported for other ocean regions. Surface excesses of DOC and DON were calculated against nearly constant subsurface concentrations. A consistent contribution of low C/N ratio (2.7–5.0) was found in the mid-surface layer (30–75 m), suggesting more extensive degradation of carbon-enriched materials and/or enhanced supply of nitrogen-enriched ones.     

The influence of the south-west monsoon upon the nutrient biogeochemistry of the Arabian Sea

Variations in the nutrient concentrations were studied during two cruises to the Arabian Sea. The situation towards the end of the southwest monsoon season (September/October 1994) was compared with the inter-monsoonal season during November and December 1994. Underway surface transects showed the influence of an upwelling system during the first cruise with deep, colder, nutrient-rich water being advected into the surface mixed layer. During the southwesterly monsoon there was an area of coastal Ekman upwelling, bringing colder water (24.2°C) into the surface waters of the coastal margin. Further offshore at about 350 km there was an area of Ekman upwelling, as a result of wind-stress curl, north of the Findlater Jet axis; this area also had cooler surface water (24.6°C). Further offshore (>1000 km) the average surface temperatures increased to >27°C. These waters were oligotrophic with no evidence of the upwelling effects observed further inshore. In the upwelling regions nutrient concentrations in the close inshore coastal zone were elevated (NO₃=18 μmol l^-1, PO₄=1.48 μmol l^-1); higher concentrations also were measured at the region of offshore upwelling off the shelf, with a maximum nitrate concentration of 12.5 μmol l^-1 and a maximum phosphate concentration of 1.2 μmol l^-1. Nitrate and phosphate concentrations decreased with increasing distance offshore to the oligotrophic waters beyond 1400 km, where typical nitrate concentrations were 35.0 nmol l^-1 (0.035 μmol l^-1) in the surface mixed layer. A CTD section from the coastal shelf, to 1650 km offshore to the oligotrophic waters, clearly showed that during the monsoon season, upwelling is one of the major influences upon the nutrient concentrations in the surface waters of the Arabian Sea off the coast of Oman. Productivity of the water column was enhanced to a distance of over 800 km offshore. During the intermonsoon period a stable surface mixed layer was established, with a well-defined thermocline and nitracline. Surface temperature was between 26.8 and 27.4°C for the entire transect from the coast to 1650 km offshore. Nitrate concentrations were typically between 2.0 and 0.4 μmol l^-1 for the transect, to about 1200 km where the waters became oligotrophic, and nitrate concentrations were then typically 8–12 nmol l^-1. Ammonia concentrations for the oligotrophic waters were typically 130 nmol l^-1, and are reported for the first time in the Indian Ocean. The nitrogen/phosphorus (N/P) ratios suggest that phytoplankton production was potentially nitrogen-limited in all the surface waters of the Arabian Sea, with the greatest nitrogen limitation during the intermonsoon period.     

Fate of biogenic carbon in the upper 200 m of the central Greenland Sea

Sedimentation of particulate carbon from the upper 200–300 m in the central Greenland Sea from August 1993 to June 1995 was less than 2 g C m⁻² yr⁻¹. Daily rates of sedimentation of particulate organic carbon reached highest values of about 18 mg m⁻² d⁻¹ in fall 1994. For total particulate material, maximum rates of sedimentation of about 250 mg m⁻² d⁻¹ were recorded in spring and fall 1994. For chlorophyll equivalent, highest rates of sedimentation of about 140 μg m⁻² d⁻¹ were recorded in spring 1994. As reported in related investigations, the transient accumulation of DOC in surface waters during summer, as well as respiration and mortality of deep overwintering zooplankton stocks, appeared to dominate the fate of photosynthetically fixed organic carbon. The above processes may account for roughly 43 g C m⁻² in the upper 200 m of the central Greenland Sea. For comparison, the seasonal deficit in dissolved inorganic carbon was reported to be about 23 g C m⁻² in the upper 20 m of surface water, and estimates for new annual production were reported to be about 57 g C m⁻². In our investigation, the biological carbon pump was not unusually effective in transporting carbon out of the productive surface layer.     

Viral abundance and distribution in mesopelagic and bathypelagic waters of the Mediterranean Sea

Despite the fact that marine viruses have been increasingly investigated in the last decade, knowledge on virus abundance, biomass and distribution in mesopelagic and bathypelagic waters is limited. We report here the results of a large-spatial-scale study (covering more than 3000 km) on the virioplankton distribution in epi-, meso- and bathypelagic waters in 19 areas of the Mediterranean Sea, from the Alboran Sea and Western Mediterranean, to the Tyrrhenian Sea, Sicily Channel and Ionian Sea. Integrated viral abundance in epipelagic waters was significantly higher than in deep-sea waters (on average, 2.4 vs. 0.5×10¹² viruses m⁻³). However, abundance of viruses in the deep-Mediterranean waters was the highest reported so far for deep seas worldwide (7.0 and 3.1×10¹¹ viruses m⁻³ in mesopelagic and bathypelagic waters, respectively) and their biomass accounted for 13–18% of total prokaryotic C biomass. The significant relationship between viral abundance and prokaryotic abundance and production in deep waters suggests that also deep-sea viruses are closely dependent on the abundance and metabolism of their hosts. Moreover, virus to prokaryote (and nucleoid-containing cell (NuCC)) abundance ratio increased with increasing depths suggesting that deep waters may represent optimal environments for viral survival or proliferation. Overall, our results indicate that deep waters may represent a significant reservoir of viruses and open new perspectives for future investigations of viral impact on the functioning of meso-bathypelagic ecosystems.     

Microbial respiration in the Levantine Sea: evolution of the oxidative processes in relation to the main Mediterranean water masses

First data on microbial respiration in the Levantine Sea are reported with the aim of assessing the distribution of oxidative processes in association with the main Mediterranean water masses and the changing physical structure determined by the Eastern Mediterranean Transient. Respiratory rates, in terms of metabolic carbon dioxide production, were estimated from measured electron transport system activities in the polygonal area of the Levantine Sea (32.5–36.5 N Latitude, 26.0–30.25 E Longitude) and at Station Geo’95, in the Ionian Sea (35°34.88 N; 17°14.99 E). At the Levantine Sea, the mean carbon dioxide production rate decreased from the upper to the deeper layers and varied from 22.0±12.4 μg C h⁻¹ m⁻³ in the euphotic layer to 1.30±0.5 μg C h⁻¹ m⁻³ in the depth range between 1600 and 3000 m. Significant differences were found among upper, intermediate and bottom layers. The euphotic zone supported a daily carbon dioxide production of 96.6 mg C d⁻¹ m⁻² while the aphotic zone (between 200 and 3000 m) sustained a 177.1 mg C d⁻¹ m⁻² carbon dioxide production. In Station Geo’95, the carbon dioxide production rates amounted to 170.4 and 102.2 mg C d⁻¹ m⁻² in the euphotic and aphotic zones, respectively. The rates determined in the identified water masses showed a tight coupling of respiratory processes and Mediterranean circulation patterns. The increasing respiratory rates in the deep layers of the Levantine Sea are explained by the introduction of younger waters recently formed in the Aegean Sea.     

Temporal dynamics of dissolved combined neutral sugars and the quality of dissolved organic matter in the Northwestern Sargasso Sea

The dynamics of dissolved combined neutral sugars (DCNS) were assessed in the upper 250 m at the Bermuda Atlantic Time-series Study (BATS) site between 2001 and 2004. Our results reveal a regular annual pattern of DCNS accumulation with concentrations increasing at a rate of 0.009–0.012 μmol C L^?1 d^?1 in the surface 40 m from March to July and reaching maximum mean concentrations of 2.2–3.3 μmol C L^?1. Winter convective mixing (between January and March) annually exported surface-accumulated DCNS to the upper mesopelagic zone (100–250 m), as concentrations increased there by 0.3–0.6 μmol C L^?1. The exported DCNS was subsequently removed over a period of weeks following restratification of the water column. Vertical and temporal trends in DCNS yield (% of DOC) supported its use as a diagenetic indicator of DOM quality. Higher DCNS yields in surface waters suggested a portion of the DOM accumulated relatively recently compared to the more recalcitrant material of the upper mesopelagic that had comparably lower yields. DCNS yields and mol% neutral sugar content, together, indicated differences in the diagenetic state of the surface-accumulated and deep pools of DOM. Seasonally accumulated, recently produced DOM with higher DCNS yields was characterized by elevated mol% of galactose and mannose+xylose levels. Conversely, more recalcitrant DOM from depths >100 m had lower DCNS yields but higher mol% of glucose. Lower DCNS yields and elevated mol% glucose were also observed in the surface waters during winter convective mixing, indicating an entrainment of a diagenetically altered DOM pool into the upper 100 m. A multivariate statistical analysis confirms the use of DCNS as an index of shifts in DOM quality at this site.     

Evaluation of the budget for silicic acid in Cascadia Basin deep water

Between 2 and 3 km depth, North Pacific deep waters contain a plume of water with high silicic acid concentrations. The plume extends outward from Cascadia Basin (the Washington Margin), where waters can contain in excess of 200 μM off the coast of Oregon and Washington. To identify the source of the high Si concentrations in Cascadia Basin, we measured silicic acid and germanium concentrations in deep waters, and their fluxes from sediments using incubated cores. The mean flux of silicic acid into bottom waters is 0.81±0.05 mmol/m²-day, and the Ge/Si ratio of this flux is 0.7±0.1 μmol/mol. A box model, incorporating these results with hydrographic data, indicates that (1) no more than 5% of the silicic acid added to Basin deep waters can have a hydrothermal source (either hot or warm seeps), and (2) the total input of silicic acid to Basin deep waters is 0.06±0.02 Tmol/y. This input is nearly all from remineralized biogenic debris and should contribute about 0.5% of the 14 Tmol/y that are estimated to be necessary to maintain the North Pacific plume.     

Rapid removal of terrigenous dissolved organic carbon over the Eurasian shelves of the Arctic Ocean

The fate of terrigenous dissolved organic carbon (tDOC) delivered to the Arctic Ocean by rivers remains poorly constrained on both spatial and temporal scales. Early reports suggested Arctic tDOC was refractory to degradation, while recent studies have shown tDOC removal to be an active but slow process. Here we present observations of DOC, salinity, δ¹⁸O, and ²²⁸Ra/²²⁶Ra in the Polar Surface Layer (PSL) over the outer East Siberian/Chukchi shelf and the adjacent Makarov and Eurasian basins of the eastern Arctic Ocean. This off-shelf system receives meteoric water, introduced by rivers, after a few years residence on the shelf. Elevated concentrations of DOC (> 120 μM C) were observed in low salinity (~ 27) water over the Makarov Basin, suggesting inputs of tDOC-enriched river water to the source waters of the Transpolar Drift. The regression of DOC against salinity indicated an apparent tDOC concentration of 315 ± 7 μM C in the river water fraction, which is significantly lower than the estimated DOC concentration in the riverine sources to the region (724 ± 55 μM C). To obtain the timescale of removal, estimates of shelf residence were coupled with measurements of dissolved ²²⁸Ra/²²⁶Ra, an isotopic tracer of time since shelf residence. Shelf residence time coupled with DOC distributions indicates a first order tDOC removal rate constant, λ = 0.24 ± 0.07 yr^-1, for the eastern Arctic, 2.5–4 times higher than rates previously observed in the western Arctic. The observed removal of tDOC in the eastern Arctic occurs over the expansive shelf area, highlighting the initial lability of tDOC upon delivery to the Arctic Ocean, and suggests that tDOC is composed of multiple compartments defined by reactivity. The relatively rapid remineralization of tDOC on the shelves may mitigate the strength of the Arctic Ocean atmospheric CO₂ sink if a projected increase in labile tDOC flux occurs.     

Deep Caribbean Sea warming

Data collected from hydrographic stations occupied within the Venezuelan and Columbian basins of the Caribbean Sea from 1922 through 2003 are analyzed to study the decadal variability of deep temperature in the region. The analysis focuses on waters below the 1815-m sill depth of the Anegada–Jungfern Passage. Relatively dense waters (compared to those in the deep Caribbean) from the North Atlantic spill over this sill to ventilate the deep Caribbean Sea. Deep warming at a rate of over 0.01 °C decade^–1 below this sill depth appears to have commenced in the 1970s after a period of relatively constant deep Caribbean Sea temperatures extending at least as far back as the 1920s. Conductivity–temperature–depth station data from World Ocean Circulation Experiment Section A22 along 66°W taken in 1997 and again in 2003 provide an especially precise, albeit geographically limited, estimate of this warming over that 6-year period. They also suggest a small (0.001 PSS-78, about the size of expected measurement biases) deep freshening. The warming is about 10 times larger than the size of geothermal heating in the region, and is of the same magnitude as the average global upper-ocean heat uptake over a recent 50-year period. Together with the freshening, the warming contributes about 0.012 m decade^–1 of sea level rise in portions of the Caribbean Sea with bottom depths around 5000 m.     

Nitrous oxide and N-nutrient cycling in the oxygen minimum zone off northern Chile

Measurements of dissolved gases (O₂, N₂O), nutrients (NO₃⁻, NO₂⁻, PO₄³⁻), and oceanographic variables were performed off northern Chile (∼21°S) between March 2000 and July 2004, in order to characterize the existing oxygen minimum zone (OMZ) and identify processes involved in N₂O cycling. Both N₂O and NO₃⁻ displayed sharp, shallow peaks with concentrations of up to 124 nM (1370% saturation) and 26 μM, respectively, in association with a strong oxycline that impinges on the euphotic zone. NO₂⁻ accumulation below the oxycline's base reached up to 9 μM. The vertical distribution of physical and chemical parameters and the existing relationships between apparent oxygen utilization (AOU), apparent N₂O production (ΔN₂O), and NO₃⁻ revealed three main layers within the upper OMZ. The first layer, or the upper part of the oxycline, is located between the base of the mixed layer and the mid-point of the oxycline (around σ_t=25.5 kg m⁻³). There the O₂ declines from ∼250 to ∼50 μM, and strong (but opposing) O₂ and NO₃⁻ gradients and their associated AOU–ΔN₂O and AOU–NO₃⁻ relationships indicate that nitrification produces N₂O and NO₃⁻ in the presence of light. The second layer, or lower part of the oxycline, represents the upper OMZ boundary and is located between the middle and the base of the oxycline (25.9<σ_t<26.1 kg m⁻³). In this layer NO₃⁻ reduction begins at O₂ levels ranging from ∼50 to ∼11 μM and accumulation of 41–68% of the ΔN₂O pool occurs. The accumulation of N₂O (but not of NO₂⁻ or NH₄⁺) and the observed AOU–ΔN₂O and AOU–NO₃⁻ relationships (which are opposite to those of the overlying first layer) suggest that a coupling between nitrification and NO₃⁻ reduction is involved in N₂O cycling in this second layer. The third layer is the OMZ core, where the O₂ concentration remains constant (O₂<11 μM). It coincides with σ_t>26.2 kg m⁻³, which is typical of Equatorial Subsurface Water (ESSW). In this layer, N₂O and NO₃⁻ continue to decrease, but a large NO₂⁻ accumulation is observed. Considering all the data, a biogeochemical model for the upper OMZ off northern of Chile is proposed, in which nitrification and denitrification differentially mediate N₂O cycling in each layer.     

Net community production in the northeastern Chukchi Sea

To assess the magnitude, distribution and fate of net community production (NCP) in the Chukchi Sea, dissolved inorganic carbon (DIC), dissolved organic carbon (DOC) and dissolved organic nitrogen (DON), and particulate organic carbon (POC) and particulate organic nitrogen (PON) were measured during the spring and summer of 2004 and compared to similar observations taken in 2002. Distinctive differences in hydrographic conditions were observed between these two years, allowing us to consider several factors that could impact NCP and carbon cycling in both the Chukchi Shelf and the adjacent Canada Basin. Between the spring and summer cruises high rates of phytoplankton production over the Chukchi shelf resulted in a significant drawdown of DIC in the mixed layer and the associated production of DOC/N and POC/N. As in 2002, the highest rates of NCP occurred over the northeastern part of the Chukchi shelf near the head of Barrow Canyon, which has historically been a hotspot for biological activity in the region. However, in 2004, rates of NCP over most of the northeastern shelf were similar and in some cases higher than rates observed in 2002. This was unexpected due to a greater influence of low-nutrient waters from the Alaskan Coastal Current in 2004, which should have suppressed rates of NCP compared to 2002. Between spring and summer of 2004, normalized concentrations of DIC in the mixed layer decreased by as much as 280 μmol kg⁻¹, while DOC and DON increased by ∼16 and 9 μmol kg⁻¹, respectively. Given the decreased availability of inorganic nutrients in 2004, rates of NCP could be attributed to increased light penetration, which may have allowed phytoplankton to increase utilization of nutrients deeper in the water column. In addition, there was a rapid and extensive retreat of the ice cover in summer 2004 with warmer temperatures in the mixed layer that could have enhanced NCP. Estimates of NCP near the head of Barrow Canyon in 2004 were ∼1500 mg carbon (C) m⁻² d⁻¹ which was ∼400 mg C m⁻² d⁻¹ higher than the same location in 2002. Estimates of NCP over the shelf-break and deep Canada Basin were low in both years, confirming that there is little primary production in the interior of the western Arctic Ocean due to near-zero concentrations of inorganic nitrate in the mixed layer.     

Tracing dissolved organic matter cycling in the eastern boundary of the temperate North Atlantic using absorption and fluorescence spectroscopy

Apparent oxygen utilization (AOU), dissolved organic carbon (DOC), coloured dissolved organic matter (CDOM) absorption spectra, and CDOM fluorescence characteristic of aromatic amino acids (excitation/emission 280 nm/320 nm; F(280/320)) and marine-humic like substances (320 nm/410 nm; F(320/410)) were measured in full depth during a cruise in the temperate Eastern North Atlantic (ENA). An optimum multi-parameter (OMP) inverse method was run to calculate water mass proportion-weighted average (archetypal) concentrations of these chemical parameters for all water masses and samples. Archetypal concentrations retain the variability due to water mass mixing and basin scale mineralization from the water mass formation sites to the study area. Conversely, the difference between measured and archetypal concentrations, retain the variability due to dissimilarities in mineralization processes within the study area. Our analysis indicates that DOC supported 26±3% of the AOU in the dark temperate ENA and that basin scale processes occurring at and from the formation area of the water masses explained 63% of the total DOC variability. Our data also suggests that DOC remineralized at the basin scale was of lower molecular weight, and with a lower proportion of fluorescent aromatic amino acids than found within the study area. The relationship between the absorption coefficient at 254 nm (a_CDOM(254)) and AOU indicates that a_CDOM(254) was consumed during organic matter remineralization in the dark ocean, with 55% of the variability being explained by basin scale processes. The relationships of F(320/410) with AOU and DOC confirmed that marine humic-like substances are produced by microbial degradation processes, at a rate of 6.1±0.9×10⁻³ mg equivalents of QS mol AOU⁻¹. Our results also indicate that basin-scale remineralization processes account for 85% of the total variability of F(320/410), emphasizing that large scale processes control the formation of humic-like substance in the dark ENA.     

Seasonal variability of dissolved oxygen,percent oxygen saturation,and apparent oxygen utilization in the Atlantic and Pacific Oceans

Using objectively analyzed seasonal fields of dissolved oxygen content, percent oxygen saturation, and apparent oxygen utilization (AOU), we describe the large-scale seasonal variability of oxygen for the Atlantic and Pacific Oceans in the upper 400 m. The winter minus summer basin zonal averages of AOU reveal a two-layer feature in both the Atlantic and the Pacific, for both hemispheres. Biological activity and seasonal stratification in the summer give the upper 50–75 m of the water column in each basin a lower AOU in summer than winter. Greater mixing of upper ocean waters in winter gives the 75–400 m layer lower AOU values in that season. The basin integral seasonal volumes of oxygen for both the North Atlantic and the North Pacific mirror what is occurring in the atmosphere, indicating that there is a seasonal flux of oxygen across the air–sea interface. Winter total O₂ volume in the ocean is above the annual mean; the summer volume is below. Larger seasonal differences in the total O₂ content are observed in the North Atlantic Ocean than the North Pacific Ocean. A seasonal net outgassing (SNO) of 8.3×10¹⁴ moles O₂ is calculated from basin means, which is 25% higher than previous results.     

On the possibility of iodide oxidation in the near-surface of the Black Sea and its implications to iodine in the general ocean

Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10⁻⁴ mol I m⁻² a⁻¹. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO₃⁻/I⁻ and I₂/I⁻ couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.     

Phytoplankton of the western Arctic in the spring and summer of 2002: Structure and seasonal changes

We analyzed the taxonomic structure and spatial variability of phytoplankton abundance and biomass in the Chukchi and Beaufort Seas during spring and summer seasons of the SBI program. Phytoplankton samples were collected during two surveys from May 10 to June 13 and from July 19 to August 21 of 2002. In May and June, ice cover exceeded 80% over most of the study area and there was no vertical stratification, indicating that the successional state of the phytoplankton corresponded to the end of the winter biological season. The phytoplankton abundance ranged from a few tens to a few thousands of cells per liter, while biomass varied from 0.1 to 3.0 mg C m⁻³. Small areas of high phytoplankton abundance (0.13–1.3×10⁶ cells L⁻¹) and biomass (22–536 mg C m⁻³), dominated by early spring diatoms Pauliella taeniata and Fragilariopsis oceanica in the surface waters, which indicated the beginning of the spring bloom, were observed only in the southeastern part of the Chukchi shelf and off Point Barrow. In July and August summer period, more than a half of the study area had <50% ice cover and the water column was stratified by temperature and salinity. Over the Chukchi shelf and continental slope of the Beaufort Sea, the phytoplankton abundance and biomass were an order of magnitude higher in July–August than in May–June. The taxonomic diversity of algae also increased due to the appearance of late-spring and summer diatoms, dinoflagellates, and coccolithophorids (Emiliania huxleyi). Interestingly, the seasonal differences between phytoplankton abundance and taxonomic composition in the spring and summer periods varied the least over the Chukchi Sea slope and in the deep-water area of the Arctic Ocean. High algae concentrations in summer were located in the lower layers of the euphotic zone, suggesting that the spring bloom on both the Chukchi shelf and in the western part of the Beaufort Sea occurred in late June/early July. In the spring and summer, the microalgal community was characterized by a high abundance of 4–10 μm flagellates, which exceeded the abundance of all other taxonomic groups. In both seasons studied, phytoplankton reached its maximum abundance within restricted areas in the southern part of the Chukchi Sea southwest of Point Hope, in the northern part of the Chukchi shelf between the 50- and 100-m isobaths, on the shelf northwest of Point Barrow, and over the continental slope in the Beaufort Sea. The pronounced spatial difference in the seasonal state was a characteristic feature of the phytoplankton community in the western Arctic.     

Biogeochemical study of a coccolithophore bloom in the northern Bay of Biscay (NE Atlantic Ocean) in June 2004

The present paper synthesizes data obtained during a multidisciplinary cruise carried out in June 2004 at the continental margin of the northern Bay of Biscay. The data-set allows to describe the different stages of a coccolithophore bloom dominated by Emiliania huxleyi. The cruise was carried out after the main spring phytoplankton bloom that started in mid-April and peaked in mid-May. Consequently, low phosphate (PO₄ < 0.2 μM) and silicate (DSi < 2.0 μM) concentrations, low partial pressure of carbon dioxide (pCO₂) and high calcite saturation degree in surface waters combined with thermal stratification, probably favoured the blooming of coccolithophores. During the period of the year our cruise was carried out, internal tides induce enhanced vertical mixing at the continental shelf break leading to the injection of inorganic nutrients to surface waters that probably trigger the bloom. The bloom developed as the water-column stratified and as the water mass was advected over the continental shelf, following the general residual circulation in the area. The most developed phase of the bloom was sampled in a remote sensed high reflectance (HR) patch over the continental shelf that was characterized by low chlorophyll-a (Chl-a) concentration in surface waters (<1.0 μg L^?1), high particulate inorganic carbon (PIC) concentration (～8 μmol L^?1) and coccolithophore abundance up to 57 × 10⁶ cells L^?1. Transparent exopolymer particles (TEP) concentrations ranged between 15 and 75 μg C L^?1 and carbon content of TEP represented up to 26% of the particulate organic carbon (POC; maximum concentration of 15.5 μmol L^?1 in the upper 40 m). Integrated primary production (PP) ranged between 210 and 680 mg C m^?2 d^?1 and integrated calcification (CAL) ranged between 14 and 140 mg C m^?2 d^?1, within the range of PP and CAL values previously reported during coccolithophore blooms in open and shelf waters of the North Atlantic Ocean. Bacterial protein production (BPP) measurements in surface waters (0.3–0.7 μg C L^?1 h^?1) were much higher than those reported during early phases of coccolithophore blooms in natural conditions, but similar to those during peak and declining coocolithophorid blooms reported in mesocosms. Total alkalinity anomalies with respect to conservative mixing (ΔTA) down to ?49 μmol kg^?1 are consistent with the occurrence of biogenic precipitation of calcite, while pCO₂ remained 15–107 μatm lower than atmospheric equilibrium (372 μatm). The correlation between ΔTA and pCO₂ suggested that pCO₂ increased in part due to calcification, but this increase was insufficient to overcome the background under-saturation of CO₂. This is related to the biogeochemical history of the water masses due to net carbon fixation by the successive phytoplankton blooms in the area prior to the cruise, hence, the investigated area remained a sink for atmospheric CO₂ despite calcification.