scholarly journals Processes controlling the Si-isotopic composition in the Southern Ocean and application for paleoceanography

2012 ◽  
Vol 9 (7) ◽  
pp. 2443-2457 ◽  
Author(s):  
F. Fripiat ◽  
A.-J. Cavagna ◽  
F. Dehairs ◽  
A. de Brauwere ◽  
L. André ◽  
...  

Abstract. Southern Ocean biogeochemical processes have an impact on global marine primary production and global elemental cycling, e.g. by likely controlling glacial-interglacial pCO2 variation. In this context, the natural silicon isotopic composition (δ30Si) of sedimentary biogenic silica has been used to reconstruct past Si-consumption:supply ratios in the surface waters. We present a new dataset in the Southern Ocean from a IPY-GEOTRACES transect (Bonus-GoodHope) which includes for the first time summer δ30Si signatures of suspended biogenic silica (i) for the whole water column at three stations and (ii) in the mixed layer at seven stations from the subtropical zone up to the Weddell Gyre. In general, the isotopic composition of biogenic opal exported to depth was comparable to the opal leaving the mixed layer and did not seem to be affected by any diagenetic processes during settling, even if an effect of biogenic silica dissolution cannot be ruled out in the northern part of the Weddell Gyre. We develop a mechanistic understanding of the processes involved in the modern Si-isotopic balance, by implementing a mixed layer model. We observe that the accumulated biogenic silica (sensu Rayleigh distillation) should satisfactorily describe the δ30Si composition of biogenic silica exported out of the mixed layer, within the limit of the current analytical precision on the δ30Si. The failures of previous models (Rayleigh and steady state) become apparent especially at the end of the productive period in the mixed layer, when biogenic silica production and export are low. This results from (1) a higher biogenic silica dissolution:production ratio imposing a lower net fractionation factor and (2) a higher Si-supply:Si-uptake ratio supplying light Si-isotopes into the mixed layer. The latter effect is especially expressed when the summer mixed layer becomes strongly Si-depleted, together with a large vertical silicic acid gradient, e.g. in the Polar Front Zone and at the Polar Front.

2011 ◽  
Vol 8 (5) ◽  
pp. 10155-10185 ◽  
Author(s):  
F. Fripiat ◽  
A.-J. Cavagna ◽  
F. Dehairs ◽  
A. de Brauwere ◽  
L. André ◽  
...  

Abstract. Southern Ocean biogeochemical processes have an impact on global marine primary production and global elemental cycling, e.g. by likely controlling glacial-interglacial pCO2 variation. The natural silicon isotopic composition (δ30Si) of sedimentary biogenic silica has been used to reconstruct past Si-consumption:supply ratio in the surface waters. We present a new dataset in the Southern Ocean which includes for the first time summer δ30Si signatures of suspended biogenic silica (i) for the whole water column at three stations and (ii) in the mixed layer at seven stations from the sub-tropical zone up to the Weddell Gyre. In general, the biogenic silica isotopic composition at depth reflected a mixed layer origin and seemed not affected by any diagenetic effect in the water column, even if in the northern part of the Weddell Gyre an effect of biogenic silica dissolution cannot be ruled out. We develop a mechanistic understanding of the processes involved in the modern Si-isotopic balance, by implementing a mixed layer model. We observe that the accumulated biogenic silica (sensu Rayleigh) should satisfactorily describe the δ30Si composition of biogenic silica exported out of the mixed layer, within the limit of the current analytical precision on the δ30Si. The failures of previous models (Rayleigh and steady state) become apparent especially at the end of the productive period in the mixed layer, when biogenic silica production is low. This results from: (1) a higher biogenic silica dissolution:production ratio imposing a lower net fractionation factor and (2) a higher Si-supply:Si-uptake ratio supplying light Si-isotopes into the mixed layer. The latter effect is especially expressed when the summer mixed layer becomes strongly Si-depleted together with a large vertical silicic acid gradient.


Ocean Science ◽  
2011 ◽  
Vol 7 (5) ◽  
pp. 533-547 ◽  
Author(s):  
F. Fripiat ◽  
A.-J. Cavagna ◽  
F. Dehairs ◽  
S. Speich ◽  
L. André ◽  
...  

Abstract. Silicon isotopic signatures (δ30Si) of water column silicic acid (Si(OH)4) were measured in the Southern Ocean, along a meridional transect from South Africa (Subtropical Zone) down to 57° S (northern Weddell Gyre). This provides the first reported data of a summer transect across the whole Antarctic Circumpolar Current (ACC). δ30Si variations are large in the upper 1000 m, reflecting the effect of the silica pump superimposed upon meridional water transfer across the ACC: the transport of Antarctic surface waters northward by a net Ekman drift and their convergence and mixing with warmer upper-ocean Si-depleted waters to the north. Using Si isotopic signatures, we determine different mixing interfaces: the Antarctic Surface Water (AASW), the Antarctic Intermediate Water (AAIW), and thermoclines in the low latitude areas. The residual silicic acid concentrations of end-members control the δ30Si alteration of the mixing products and with the exception of AASW, all mixing interfaces have a highly Si-depleted mixed layer end-member. These processes deplete the silicic acid AASW concentration northward, across the different interfaces, without significantly changing the AASW δ30Si composition. By comparing our new results with a previous study in the Australian sector we show that during the circumpolar transport of the ACC eastward, the δ30Si composition of the silicic acid pools is getting slightly, but significantly lighter from the Atlantic to the Australian sectors. This results either from the dissolution of biogenic silica in the deeper layers and/or from an isopycnal mixing with the deep water masses in the different oceanic basins: North Atlantic Deep Water in the Atlantic, and Indian Ocean deep water in the Indo-Australian sector. This isotopic trend is further transmitted to the subsurface waters, representing mixing interfaces between the surface and deeper layers. Through the use of δ30Si constraints, net biogenic silica production (representative of annual export), at the Greenwich Meridian is estimated to be 5.2 ± 1.3 and 1.1 ± 0.3 mol Si m−2 for the Antarctic Zone and Polar Front Zone, respectively. This is in good agreement with previous estimations. Furthermore, summertime Si-supply into the mixed layer of both zones, via vertical mixing, is estimated to be 1.6 ± 0.4 and 0.1 ± 0.5 mol Si m−2, respectively.


2016 ◽  
Vol 13 (21) ◽  
pp. 6049-6066 ◽  
Author(s):  
Ivia Closset ◽  
Damien Cardinal ◽  
Mathieu Rembauville ◽  
François Thil ◽  
Stéphane Blain

Abstract. 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).


2011 ◽  
Vol 8 (2) ◽  
pp. 639-674 ◽  
Author(s):  
F. Fripiat ◽  
A.-J. Cavagna ◽  
F. Dehairs ◽  
S. Speich ◽  
L. André ◽  
...  

Abstract. Water column silicon isotopic signatures (δ30Si) of silicic acid (Si(OH)4) in the Southern Ocean were measured along a meridional transect from South Africa (Subtropical Zone) down to 57° S (northern Weddell Gyre). These data are the first reported for a summer transect across the whole Antarctic Circumpolar Current (ACC). δ30Si variations are large in the upper 1000 m, reflecting the effect of the silica pump superimposed upon meridional transfer across the ACC: the transport of Antarctic surface waters northward by a net Ekman drift and their convergence and mixing with warmer upper-ocean Si-depleted waters to the north. Using Si isotopic signatures, we determined different mixing interfaces between ACC water masses: the Antarctic Surface Water (AASW), the Antarctic Intermediate Water (AAIW), and the thermoclines in the low latitude areas. The residual silicic acid concentrations of end-members control the δ30Si alteration of the mixing products. With the exception of AASW, all mixing interfaces have a highly Si-depleted mixed layer end-member. These processes deplete the silicic acid AASW concentration across the different interfaces northward without significantly changing the AASW δ30Si. By comparing our new results with a previous study in the Australian sector we show that during the circumpolar transport of the ACC eastward, there is a slight but significant Si-isotopic lightening of the silicic acid pools from the Atlantic to the Australian sectors. This results either from the dissolution of biogenic silica in the deeper layers and/or from an isopycnal mixing with the deep water masses in the different oceanic basins: North Atlantic Deep Water in the Atlantic, and Indian Ocean deep water in the Indo-Australian sector. This eastward lightening is further transmitted to the subsurface waters, representing mixing interfaces between the surface and deeper layers. Using the Si-isotopic constraint, we estimate for the Greenwich Meridian a net biogenic silica production which should be representative of the annual export, at 4.5 ± 1.1 and 1.5 ± 0.4 mol Si m−2 for the Antarctic Zone and Polar Front Zone, respectively, in agreement with previous estimations. The summertime Si-supply into the mixed layer via vertical mixing was also assessed at 1.5 ± 0.4 and 0.1 ± 0.5 mol Si m−2, respectively.


2016 ◽  
Author(s):  
Ivia Closset ◽  
Damien Cardinal ◽  
Mathieu Rembauville ◽  
François Thil ◽  
Stéphane Blain

Abstract. A massive diatom-bloom is observed annually in the surface waters of the naturally Fe-fertilized Kerguelen Plateau (Southern Ocean). In this study, silicon isotopic signatures (δ30Si) of silicic acid (DSi) and suspended biogenic silica (BSi) were investigated in the whole water column with an unprecedented spatial resolution in this region, during the KEOPS-2 experiment (spring 2011). We use δ30Si measurements to track the silicon sources that fuel the bloom, and investigate the seasonal evolution of Si biogeochemical cycle in the iron fertilized area. We compare the results from a HNLC reference station with stations characterized by different degrees of iron enrichment and bloom conditions. Dissolved and particulate δ30Si signatures were generally highly variable in the upper 500 m, reflecting the effect of the intense silicon utilization in spring, while they were quite homogeneous in deeper waters. The Si-isotopic and mass balance identified a unique WW Si-source for the iron-fertilized area originating from the southeastern Kerguelen Plateau and spreading northward. However, when reaching a retroflection of the Polar Front (PF), the δ30Si composition of WW silicic acid pool was getting progressively heavier. This would result from sequential diapycnal mixings between these 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 here 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 y−1, that 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 on the Si-biogeochemical cycle since the isotopic and mass balance allows resolving the processes involved i.e. uptake, dissolution, mixing.


1997 ◽  
Vol 44 (5) ◽  
pp. 1151-1176 ◽  
Author(s):  
Christophe Rabouille ◽  
Jean-Francois Gaillard ◽  
Paul Tréguer ◽  
Marie-Anne Vincendeau

2021 ◽  
Vol 8 ◽  
Author(s):  
Ryan Cloete ◽  
Jean C. Loock ◽  
Natasha R. van Horsten ◽  
Susanne Fietz ◽  
Thato N. Mtshali ◽  
...  

Winter distributions of dissolved cadmium (dCd) and particulate cadmium (pCd) were measured for the first time in the Indian sector of the Southern Ocean thereby contributing a unique spatial and seasonal dataset. Seven depth profiles, between 41°S and 58°S, were collected along the 30°E longitude during the 2017 austral winter to investigate the biogeochemical cycling of cadmium during a period characterized by contrasting upper water column dynamics compared to summer. Our results support an important role for biological uptake during winter months albeit weaker compared to summer. Distinct, biologically driven changes in cadmium cycling across the transect were observed. For example, surface ratios of pCd to phosphorus (P; pCd:P) increased from 0.37 to 1.07 mmol mol–1 between the subtropical zone (STZ) and the Antarctic zone (AAZ) reflecting increased Cd requirements for diatoms at higher latitudes which, in turn, was driven by a complex relationship between the availability of dCd and dissolved iron (dFe), zinc (dZn) and manganese (dMn). Vertical profiles of pCd:P displayed near-surface maxima consistent with (1) P occurring in two phases with different labilities and the lability of Cd being somewhere in-between and (2) increasing dCd to phosphate (PO4; dCd:PO4) ratios with depth at each station. North of the Antarctic Polar Front (APF), a secondary, deeper pCd:P maximum may reflect an advective signal associated with northward subducting Antarctic Intermediate Water (AAIW). The strong southward increase in surface dCd and dCd:PO4, from approximately 10–700 pmol kg–1 and 40–400 μmol mol–1, respectively, reflected the net effect of preferential uptake and regeneration of diatoms with high Cd content and the upwelling of Cd enriched water masses in the AAZ. Furthermore, distinct dCd versus PO4 relationships were observed in each of the intermediate and deep water masses suggesting that dCd and PO4 distributions at depth are largely the result of physical water mass mixing.


2013 ◽  
Vol 10 (7) ◽  
pp. 11405-11446 ◽  
Author(s):  
N. Coffineau ◽  
C. L. De La Rocha ◽  
P. Pondaven

Abstract. This study presents 6 new water column profiles of the silicon isotopic composition (δ30Si) of dissolved silicon (DSi) from the Atlantic and the Indian sectors of the Southern Ocean and a variable depth box model of silica cycling in the mixed layer constructed to illuminate the evolution of surface ocean δ30Si over the full course of a year. In keeping with previous observations, δ30Si values ranged from +1.9 to +2.4‰ in the mixed layer (ML), +1.2 to +1.7‰ in Winter Water (WW), and +0.9 to +1.4‰ in Circumpolar Deep Water (CDW). These data also confirmed the occurrence of diminished values for ML δ30Si at low DSi concentrations in early austral autumn on the Kerguelen Plateau. The box model was used to investigate whether these low, post-growing season values of δ30Si were related to input of DSi to the ML from basalt weathering, biogenic silica dissolution (with or without isotopic fractionation), the onset of winter mixing, or some combination of the three. Basalt weathering and fractionation during biogenic silica dissolution could both lower ML δ30Si below what would be expected from the extent of biological uptake of DSi. However, the key driver of the early autumn decrease in δ30Si appears to be the switch from bloom growth (with net removal of DSi and net accumulation of biogenic silica (BSi) biomass) to steady state growth (when slow but continuing production of BSi prevented significant net increase in DSi concentrations with diffusive input of DSi from WW but not decrease in ML δ30Si towards WW values). Lastly, fractionation during dissolution had only a negligible effect on the δ30Si of BSi exported throughout the course of the year, implying that seasonal changes in export efficiency (e.g., favoring the export of bloom BSi vs. the export of BSi produced during other times of the year) strongly influence the δ30Si of BSi accumulating in marine sediments. Altogether, these results suggest that as a paleoceanographic proxy, δ30Si may more reflect the dominant mode of production of the BSi that is exported (i.e. bloom vs. steady state growth) rather than strictly the extent of DSi utilization by diatoms.


2014 ◽  
Vol 11 (5) ◽  
pp. 1371-1391 ◽  
Author(s):  
N. Coffineau ◽  
C. L. De La Rocha ◽  
P. Pondaven

Abstract. This study presents six new water column profiles of the silicon isotopic composition (δ30Si) of dissolved silicon (DSi) from the Atlantic and Indian sectors of the Southern Ocean and a variable depth box model of silica cycling in the mixed layer that was constructed to illuminate the evolution of surface ocean δ30Si over the full course of a year. In keeping with previous observations, δ30Si values ranged from +1.9 to +2.4‰ in the mixed layer (ML), +1.2 to +1.7‰ in Winter Water (WW), and +0.9 to +1.4‰ in Circumpolar Deep Water (CDW). These data also confirmed the occurrence of diminished values for ML δ30Si at low DSi concentrations in early austral autumn on the Kerguelen Plateau. The box model was used to investigate whether these low, post-growing season values of δ30Si were related to input of DSi to the ML from basalt weathering, biogenic silica dissolution (with or without isotopic fractionation), the onset of winter mixing, or some combination of the three. Basalt weathering and fractionation during biogenic silica dissolution could both lower ML δ30Si below what would be expected from the extent of biological uptake of DSi. However, the key driver of the early autumn decrease in δ30Si appears to be the switch from bloom growth (with net removal of DSi and net accumulation of biogenic silica (BSi) biomass) to steady state growth (when slow but continuing production of BSi prevented significant net increase in DSi concentrations with diffusive input of DSi from WW but not decrease in ML δ30Si towards WW values). Model results also indicated that fractionation during dissolution has only a negligible effect on the δ30Si of BSi exported throughout the course of the year. However, seasonal changes in export efficiency (e.g. favouring the export of bloom BSi versus the export of BSi produced during other times of the year) should strongly influence the δ30Si of BSi accumulating in marine sediments. Finally, the choice for the parameterisation of the mixing between the ML and the WW in terms of δ30Si (i.e. constant or allowed to vary with the seasonal migration of the thermocline) is critical to take into account in box model simulations of the silica biogeochemical cycle. Altogether, these results suggest that as a paleoceanographic proxy, δ30Si may more reflect the dominant mode of production of the BSi that is exported (i.e. bloom versus steady state growth) rather than strictly the extent of DSi utilisation by diatoms.


2021 ◽  
Author(s):  
Shantelle Smith ◽  
Katye E. Altieri ◽  
Mhlangabezi Mdutyana ◽  
David R. Walker ◽  
Ruan G. Parrott ◽  
...  

Abstract. The production and consumption of ammonium (NH4+) are essential upper-ocean nitrogen cycle pathways, yet in the Southern Ocean where NH4+ has been observed to accumulate in surface waters, its mixed-layer cycling remains poorly understood. For surface samples collected between Cape Town and the marginal ice zone (MIZ) in winter 2017, we found that NH4+ concentrations were five-fold higher than is typical for summer, and lower north than south of the Subantarctic Front (SAF; 0.01–0.26 µM versus 0.19–0.70 µM). Our observations confirm that NH4+ accumulates in the Southern Ocean’s winter mixed layer, particularly in polar waters. NH4+ uptake rates were highest near the Polar Front (PF; 12.9 ± 0.4 nM day−1) and in the Subantarctic Zone (10.0 ± 1.5 nM day−1), decreasing towards the MIZ (3.0 ± 0.8 nM day−1) despite high ambient NH4+ concentrations, likely due to low sea surface temperatures and light availability. By contrast, rates of NH4+ oxidation were higher south than north of the PF (16.0 ± 0.8 versus 11.1 ± 0.5 nM day−1), perhaps due to the lower light and higher iron conditions characteristic of polar waters. Augmenting our dataset with NH4+ concentration measurements spanning the 2018/2019 annual cycle reveals that mixed-layer NH4+ accumulation south of the SAF likely derives from sustained heterotrophic NH4+ production in late summer through winter that outpaces NH4+ consumption by temperature-, light, and iron-limited microorganisms. Our observations thus imply that the Southern Ocean becomes a biological source of CO2 to the atmosphere for half the year not only because nitrate drawdown is weak, but also because the ambient conditions favour net heterotrophy and NH4+ accumulation.


Sign in / Sign up

Export Citation Format

Share Document