The Mertz Glacier Polynya off George V Land, East Antarctica, is a source of Adélie Land Bottom Water, which contributes up to ~25% of the Antarctic Bottom Water. This major polynya is closely linked ...to the presence of the Mertz Glacier Tongue that traps pack ice upstream. In 2010, the Mertz Glacier calved a massive iceberg, deeply impacting local sea ice conditions and dense shelf water formation. Here we provide the first detailed 250-year long reconstruction of local sea ice and bottom water conditions. Spectral analysis of the data sets reveals large and abrupt changes in sea surface and bottom water conditions with a ~70-year cyclicity, associated with the Mertz Glacier Tongue calving and regrowth dynamics. Geological data and atmospheric reanalysis, however, suggest that sea ice conditions in the polynya were also very sensitive to changes in surface winds in relation to the recent intensification of the Southern Annular Mode.
The distribution of dissolved silicon isotopes (δ30Si) was examined along the U.S. GEOTRACES East Pacific Zonal Transect (GP16) extending from Peru to Tahiti (10°S and 15°S latitude). Surface waters ...in the subtropical gyre displayed high δ30Si due to strong utilization of silicic acid (DSi). In contrast, surface waters close to the Peruvian coast where upwelling prevailed were less depleted and only moderately fractionated. δ30Si of water masses along the transect was compared with the results of an Optimum Multiparameter Analysis that quantified the fractional contributions of end‐member water masses in each sample. Strong admixture of intermediate waters obscured the expected heavy isotopic signatures of Subantarctic Mode Water and Antarctic Intermediate Water. Isotope values were nearly homogenous below 2,000 m (average: +1.3 ± 0.1‰, 1 s.d.) despite the 25 μmol kg−1 range in the DSi content among water masses. This homogeneity confirms prior observations and model results that predict nearly constant δ30Si values of +1.0‰ to +1.2‰ for Pacific deep waters with DSi > 100 μmol kg−1. Waters above the East Pacific Rise (EPR) influenced by hydrothermal activity showed a small increase in DSi together with dissolved iron, but overall stations close to the EPR were slightly depleted in DSi (3 to 6 μmol kg−1) with no significant shift in δ30Si compared to adjacent waters. Hydrothermal DSi appears to precipitate within the conduit of the EPR or upon contact with cold seawater resulting in a negligible influence of hydrothermal fluids on δ30Si in deep water.
Key Points
Surface waters have a large range in dissolved silicon isotopes covering nutrient‐rich coastal upwelling to oligotrophic waters
Deep water masses with DSi concentrations >100 μmol kg−1 show homogenous silicon isotope signatures despite up to 25 μmol kg−1 differences in DSi
Hydrothermal fluids have a negligible effect on Si isotope distributions in the deep Pacific
A massive diatom bloom is observed each year in the surface waters of the naturally Fe-fertilized Kerguelen Plateau (Southern Ocean). We measured biogenic silica production and dissolution fluxes ...(ρSi and ρDiss, respectively) in the mixed layer in the vicinity of the Kerguelen Plateau during austral spring 2011 (KEOPS-2 cruise). We compare results from a high-nutrient low-chlorophyll reference station and stations with different degrees of iron enrichment and bloom conditions. Above the plateau biogenic ρSi are among the highest reported so far in the Southern Ocean (up to 47.9 mmol m−2 d−1). Although significant (10.2 mmol m−2 d−1 on average), ρDiss were generally much lower than production rates. Uptake ratios (ρSi : ρC and ρSi : ρN) confirm that diatoms strongly dominate primary production in this area. At the bloom onset, decreasing dissolution-to-production ratios (D : P) indicate that the remineralization of silica could sustain most of the low silicon uptake and that the system progressively shifts toward a silica production regime which must be mainly supported by new source of silicic acid. Moreover, by comparing results from the two KEOPS expeditions (spring 2011 and summer 2005), we suggest that there is a seasonal evolution of the processes decoupling Si and N cycles in the area. Indeed, the consumption of H4SiO4 standing stocks occurs only during the growing stage of the bloom when strong net silica production is observed, contributing to higher H4SiO4 depletion relative to NO3−. Then, the decoupling of H4SiO4 and NO3− is mainly controlled by the more efficient nitrogen recycling relative to Si. Gross Si : N uptake ratios were higher in the Fe-rich regions compared to the high-nutrient low-chlorophyll (HNLC) area, likely due to different diatom communities. This suggests that the diatom responses to natural Fe fertilization are more complex than previously thought, and that natural iron fertilization over long timescales does not necessarily decrease Si : N uptake ratios as suggested by the silicic acid leakage hypothesis. Finally, we propose the first seasonal estimate of the Si biogeochemical budget above the Kerguelen Plateau based on direct measurements. This study points out that naturally iron-fertilized areas of the Southern Ocean could sustain very high regimes of biogenic silica production, similar to those observed in highly productive upwelling systems.
Although the Southern Ocean is considered a high-nutrient, low-chlorophyll (HNLC) area, massive and recurrent blooms are observed over and downstream of the Kerguelen Plateau. This mosaic of blooms ...is triggered by a higher iron supply resulting from the interaction between the Antarctic Circumpolar Current and the local bathymetry. Net primary production, N uptake (NO3− and NH4+), and nitrification rates were measured at eight stations in austral spring 2011 (October–November) during the KEOPS 2 cruise in the Kerguelen Plateau area. Natural iron fertilization stimulated primary production, with mixed layer integrated net primary production and growth rates much higher in the fertilized areas (up to 315 mmol C m−2 d−1 and up to 0.31 d−1 respectively) compared to the HNLC reference site (12 mmol C m−2 d−1 and 0.06 d−1 respectively). Primary production was mainly sustained by nitrate uptake, with f ratios (corresponding to NO3−-uptake / (NO3−-uptake + NH4+-uptake)) lying at the upper end of the observations for the Southern Ocean (up to 0.9). We report high rates of nitrification (up to ~ 3 μmol N L−1 d−1, with ~ 90 % of them < 1 μmol N L−1 d−1) typically occurring below the euphotic zone, as classically observed in the global ocean. The specificity of the studied area is that at most of the stations, the euphotic layer was shallower than the mixed layer, implying that nitrifiers can efficiently compete with phytoplankton for the ammonium produced by remineralization at low-light intensities. Nitrate produced by nitrification in the mixed layer below the euphotic zone is easily supplied to the euphotic zone waters above, and nitrification sustained 70 ± 30 % of the nitrate uptake in the productive area above the Kerguelen Plateau. This complicates estimations of new production as potentially exportable production. We conclude that high productivity in deep mixing system stimulates the N cycle by increasing both assimilation and regeneration.
We report on the zonal variability of mesopelagic particulate organic carbon remineralization and deep carbon transfer potential during the Kerguelen Ocean and Plateau compared Study 2 expedition ...(KEOPS 2; October-November 2011) in an area of the polar front supporting recurrent massive blooms from natural Fe fertilization. Mesopelagic carbon remineralization (MR) was assessed using the excess, non-lithogenic particulate barium (Baxs) inventories in mesopelagic waters and compared with bacterial production (BP), surface primary production (PP) and export production (EP). Results for this early season study are compared with the results obtained during a previous study (2005; KEOPS 1) for the same area at a later stage of the phytoplankton bloom. Our results reveal the patchiness of the seasonal advancement and of the establishment of remineralization processes between the plateau (A3) and polar front sites during KEOPS 2. For the Kerguelen plateau (A3 site) we observe a similar functioning of the mesopelagic ecosystem during both seasons (spring and summer), with low and rather stable remineralization fluxes in the mesopelagic column (150-400 m). The shallow water column (~500 m), the lateral advection, the zooplankton grazing pressure and the pulsed nature of the particulate organic carbon (POC) transfer at A3 seem to drive the extent of MR processes on the plateau. For deeper stations (>2000 m) located on the margin, inside a polar front meander, as well as in the vicinity of the polar front, east of Kerguelen, remineralization in the upper 400 m in general represents a larger part of surface carbon export. However, when considering the upper 800 m, in some cases, the entire flux of exported carbon is remineralized. In the polar front meander, where successive stations form a time series, two successive events of particle transfer were evidenced by remineralization rates: a first mesopelagic and deep transfer from a past bloom before the cruise, and a second transfer expanding at mesopelagic layers during the cruise. Regarding the deep carbon transfer efficiency, it appeared that above the plateau (A3 site) the mesopelagic remineralization was not a major barrier to the transfer of organic matter to the seafloor (close to 500 m). There, the efficiency of carbon transfer to the bottom waters (>400 m) as assessed by PP, EP and MR fluxes comparisons reached up to 87% of the carbon exported from the upper 150 m. In contrast, at the deeper locations, mesopelagic remineralization clearly limited the transfer of carbon to depths of >400 m. For sites at the margin of the plateau (station E-4W) and the polar front (station F-L), mesopelagic remineralization even exceeded upper 150 m export, resulting in a zero transfer efficiency to depths >800 m. In the polar front meander (time series), the capacity of the meander to transfer carbon to depth >800 m was highly variable (0 to 73%). The highest carbon transfer efficiencies in the meander are furthermore coupled to intense and complete deep (>800 m) remineralization, resulting again in a near-zero, deep (>2000 m) carbon sequestration efficiency there.
Tracking variations in the surface ocean supply and demand of nitrate, a key marine nutrient, can help constrain the contribution of biological production in driving past climate shifts. The nitrogen ...isotopic composition (as δ15N) of organic matter in marine sediments is a proxy for surface ocean nitrate supply and demand over time, but it may be subject to alteration during sinking and burial. The isotopic composition of nitrogen occluded in the opal shells, or frustules, of diatoms (δ15NDB) is protected and is, therefore, a potentially more robust tracer of nitrate use in the past. Here, we show that δ15NDB in Southern Ocean growout cultures of natural communities does not depend on species composition. We found that the εDB (= biomass δ15N–δ15NDB) of the community growouts was −4.8 ± 0.8‰, more than 10‰ different from previous monospecific growouts, but statistically indistinguishable from previous Southern Ocean and North Pacific surface ocean observations. The two community growouts, seeded with populations from ∼66° to ∼61°S, had distinct community compositions, but indistinguishable εDB, suggesting that species composition does not primarily set δ15NDB values, at least in Antarctic and Polar Frontal Zones of the Southern Ocean. Our results demonstrate that under nitrate‐replete conditions, δ15NDB values of frustules sinking from the surface ocean robustly track surface ocean nitrate δ15N values, and therefore nitrate supply and demand.
Key Points
In natural community growouts, δ15NDB values are higher than δ15Nbiomass values—opposite of prior monospecific diatom growouts
The relationship between δ15Nbiomass and δ15NDB was the same in community growouts and in surface ocean particles
Two distinct, diatom‐dominated Southern Ocean communities produced indistinguishable δ15NDB values, when grown on the same nitrate pool
In this study, we use IP25 and alkenone biomarker proxies to document the subdecadal variations of sea ice and sea surface temperature in the subpolar North Atlantic induced by the decadally paced ...explosive tropical volcanic eruptions of the second half of the thirteenth century. The short‐ and long‐term evolutions of both variables were investigated by cross analysis with a simulation of the IPSL‐CM5A LR model. Our results show short‐term ocean cooling and sea ice expansion in response to each volcanic eruption. They also highlight that the long response time of the ocean leads to cumulative surface cooling and subsurface heat buildup due to sea ice capping. As volcanic forcing relaxes, the surface ocean rapidly warms, likely amplified by subsurface heat, and remains almost ice free for several decades.
Key Points
ocean response to volcanism combining proxy and model data
Impact of closely spaced eruptions on SSTs and sea ice
long‐term response of high latitude ocean to volcanism
A massive diatom bloom forms annually in the surface waters of the naturally iron-fertilized Kerguelen Plateau (Southern Ocean). In this study, silicon isotopic signatures (δ30Si) of silicic acid ...(DSi) and suspended biogenic silica (BSi) were investigated through the whole water column with unprecedented spatial resolution, during the KEOPS-2 experiment (spring 2011). We used δ30Si measurements to track the sources of silicon that fuelled the bloom, and investigated the seasonal evolution of the Si biogeochemical cycle in the iron-fertilized area. We compared the results from stations with various degrees of iron enrichment and bloom conditions to an HNLC reference station. Dissolved and particulate δ30Si signatures were highly variable in the upper 500 m, reflecting the effect of intense silicon utilization in spring, while they were quite homogeneous in deeper waters. The Si isotopic and mass balance identified a unique Winter Water (WW) Si source for the iron-fertilized area that originated from southeast of the Kerguelen Plateau and spread northward. When the WW reached a retroflection of the Polar Front (PF), the δ30Si composition of the silicic acid pool became progressively heavier. This would result from sequential diapycnal and isopycnal mixings between the initial WW and ML water masses, highlighting the strong circulation of surface waters that defined this zone. When comparing the results from the two KEOPS expeditions, the relationship between DSi depletion, BSi production, and their isotopic composition appears decoupled in the iron-fertilized area. This seasonal decoupling could help to explain the low apparent fractionation factor observed in the ML at the end of summer. Taking into account these considerations, we refined the seasonal net BSi production in the ML of the iron-fertilized area to 3.0 ± 0.3 mol Si m−2 yr−1, which was exclusively sustained by surface water phytoplankton populations. These insights confirm that the isotopic composition of dissolved and particulate silicon is a promising tool to improve our understanding of the Si biogeochemical cycle since the isotopic and mass balance allows resolution of processes in the Si cycle (i.e. uptake, dissolution, mixing).
The first inter-calibration study of the stable silicon isotope composition of dissolved silicic acid in seawater, d 30 Si(OH) 4 , is presented as a contribution to the international GEOTRACES ...program. Eleven laboratories from seven countries analyzed two seawater samples from the North Pacific subtropical gyre (Station ALOHA) collected at 300 m and at 1000 m water depth. Sampling depths were chosen to obtain samples with a relatively low (9 mmol L -1 , 300 m) and a relatively high (113 mmol L -1 , 1000 m) silicic acid concentration as sample preparation differs for low- and high concentration samples. Data for the 1000 m water sample were not normally distributed so the median is used to represent the central tendency for the two samples. Median d 30 Si(OH) 4 values of +1.66‰ for the low-concentration sample and +1.25‰ for the high-concentration sample were obtained. Agreement among laboratories is overall considered very good; however, small but statistically significant differences among the mean isotope values obtained by different laboratories were detected, likely reflecting inter-laboratory differences in chemical preparation including preconcentration and purification methods together with different volumes of seawater analyzed, andthe use of different mass spectrometers including the Neptune MC-ICP-MS (Thermo Fisher™, Germany), the Nu Plasma MC-ICP-MS (Nu Instruments™, Wrexham, UK), and the Finnigan™ (now Thermo Fisher™, Germany) MAT 252 IRMS. Future studies analyzing d 30 Si(OH) 4 in seawater should also analyze and report values for these same two reference waters in order to facilitate comparison of data generated among and within laboratories over time.
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