Iron biogeochemistry in Antarctic pack ice during SIPEX-2

Our study quantified the spatial and temporal distribution of Fe and ancillary biogeochemical parameters at six stations visited during an interdisciplinary Australian Antarctic marine science voyage (SIPEX-2) within the East Antarctic first-year pack ice zone during September–October 2012. Unlike previous studies in the area, the sea ice Chlorophyll a, Particulate Organic Carbon and Nitrogen (POC and PON) maxima did not occur at the ice/water interface because of the snow loading and dynamic processes under which the sea ice formed. Iron in sea ice ranged from 0.9 to 17.4 nM for the dissolved (<0.2 µm) fraction and 0.04 to 990 nM for the particulate (>0.2 µm) fraction. Our results highlight that the concentration of particulate Fe in sea ice was highest when approaching the continent. The high POC concentration and high particulate iron to aluminium ratio in sea ice samples demonstrate that 71% of the particulate Fe was biogenic in composition. Our estimated Fe flux from melting pack ice to East Antarctic surface waters over a 30 day melting period was 0.2 µmol/m2/d of DFe, 2.7 µmol/m2/d of biogenic PFe and 1.3 µmol/m2/d of lithogenic PFe. These estimates suggest that the fertilization potential of the particulate fraction of Fe may have been previously underestimated due to the assumption that it is primarily lithogenic in composition. Our new measurements and calculated fluxes indicate that a large fraction of the total Fe pool within sea ice may be bioavailable and therefore, effective in promoting primary productivity in the marginal ice zone

Chemometric perspectives on plankton community responses to natural iron fertilisation over and downstream of the Kerguelen Plateau in the Southern Ocean

International audienceWe examined phytoplankton community responses to natural iron fertilisation at 32 sites over and downstream from the Kerguelen Plateau in the Southern Ocean during the austral spring bloom in October–November 2011. The community structure was estimated from chemical and isotopic measurements (particulate organic carbon – POC; 13C-POC; particulate nitrogen – PN; 15N-PN; and biogenic silica – BSi) on size-fractionated samples from surface waters (300, 210, 50, 20, 5, and 1 μm fractions). Higher values of 13C-POC (vs. co-located 13C values for dissolved inorganic carbon – DIC) were taken as indicative of faster growth rates and higher values of 15N-PN (vs. co-located 15N-NO3 source values) as indicative of greater nitrate use (rather than ammonium use, i.e. higher f ratios).Community responses varied in relation to both regional circulation and the advance of the bloom. Iron-fertilised waters over the plateau developed dominance by very large diatoms (50–210 μm) with high BSi / POC ratios, high growth rates, and significant ammonium recycling (lower f ratios) as biomass built up. In contrast, downstream polar frontal waters with a similar or higher iron supply were dominated by smaller diatoms (20–50 μm) and exhibited greater ammonium recycling. Stations in a deep-water bathymetrically trapped recirculation south of the polar front with lower iron levels showed the large-cell dominance observed on the plateau but much less biomass. Comparison of these communities to surface water nitrate (and silicate) depletions as a proxy for export shows that the low-biomass recirculation feature had exported similar amounts of nitrogen to the high-biomass blooms over the plateau and north of the polar front. This suggests that early spring trophodynamic and export responses differed between regions with persistent low levels vs. intermittent high levels of iron fertilisation

(Table 1) Water column silicic acid concentrations and Si isotopic composition during Marion Dufresne cruise MD166 off South Africa

Silicon isotopic signatures (d30Si) 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). d30Si 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 d30Si 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 d30Si 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 d30Si 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 d30Si 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

Silicon pool dynamics and biogenic silica export in the Southern Ocean inferred from Si-isotopes

International audienceSilicon 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

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(Table 1) Water column biogenic silica concentrations and Si isotopic composition during Marion Dufresne cruise MD166 off South Africa

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 (d30Si) 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 d30Si 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 d30Si composition of biogenic silica exported out of the mixed layer, within the limit of the current analytical precision on the d30Si. 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

Sea-ice algal primary production and nitrogen uptake rates off East Antarctica

Antarctic pack ice comprises about 90% of the sea ice in the southern hemisphere and plays an important structuring role in Antarctic marine ecosystems, yet measurements of ice algal primary production and nitrogen uptake rates remain scarce. During the early austral spring of 2012, measurements for primary production rates and uptake of two nitrogen substrates (nitrate and ammonium) were conducted at 5 stations in the East Antarctic pack ice (63–66°S, 115–125°E). Carbon uptake was low (3.52 mg C m−2 d−1) but a trend of increased production was observed towards the end of the voyage suggesting pre-bloom conditions. Significant snow covers reaching, up to 0.8 m, induced strong light limitation. Two different regimes were observed in the ice with primarily nitrate based ‘new’ production (f-ratio: 0.80–0.95) at the bottom of the ice cover, due to nutrient-replete conditions at the ice–water interface, and common for pre-bloom conditions. In the sea-ice interior, POC:PN ratios (20–70) and higher POC:Chl a ratios suggested the presence of large amounts of detrital material trapped in the ice and here ammonium was the prevailing nitrogen substrate. This suggests that most primary production in the sea-ice interior was regenerated and supported by a microbial food web, recycling detritus.info:eu-repo/semantics/publishe

Twilight zone organic carbon remineralization in the Polar Front Zone and Subantarctic Zone south of Tasmania

We report on the distribution of excess, non-lithogenic particulate barium (Baxs), a proxy for twilight zone remineralization of organic matter, in the Australian sector of the Southern Ocean during the mid-austral summer 2007. This study was part of a broader investigation focusing on macro- and micronutrient availability controlling ecosystem functioning in this area. Mesopelagic particulate excess Ba (Baxs) in the twilight zone (focus was on the 100-600m depth layer) proved to be significantly controlled by the vertical distribution of bacterial activity, with higher Baxs contents in situations where significant bacterial activity extended deeper in the water column. However, despite this covariation, the magnitude of the carbon fluxes as estimated from Baxs and bacterial activity did not match well, with carbon demand based on bacterial activity largely exceeding organic carbon remineralization estimated from Baxs. Possible reasons for this discrepancy are discussed. It appeared that the magnitude of the mesopelagic carbon remineralization flux obtained from Baxs was realistic when weighted against primary, new and export productions. Our findings corroborate earlier results indicating that mesopelagic carbon remineralization in the 100-600m depth layer increases from the Subantarctic Zone (SAZ) toward the Polar Front, and from spring to late summer. We observed furthermore that the iron-replete Subantarctic Zone east of the Tasman Plateau had a higher mesopelagic remineralization efficiency (on average 91±20% of the carbon exported from the upper 100m was remineralized before reaching 600m) compared to the Fe-limited SAZ area west of the plateau and the Polar Front Zone, where mesopelagic remineralization efficiencies ranged between 21±5% and 64±24%, respectively. SAZ-East and SAZ-West sites thus differed in their efficiency of carbon sequestration into the deep (>600m) water column, with SAZ-West exceeding the sequestration capacity of SAZ-East. © 2011 Elsevier Ltd.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Water column distribution and carbon isotopic signal of cholesterol, brassicasterol and particulate organic carbon in the Atlantic sector of the Southern Ocean

Titre original dans Biogeosciences Discussions : Whole water column distribution and carbon isotopic composition of bulk particulate organic carbon, cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre in the Southern Ocean (DOI : 10.5194/BGD-9-1667-2012)International audienceThe combination of concentrations and δ13C signatures of Particulate Organic Carbon (POC) and sterols provides a powerful approach to study ecological and environmental changes both in the modern and ancient ocean, but its application has so far been restricted to the surface area. We applied this tool to study the biogeochemical changes in the modern ocean water column during the BONUS-GoodHope survey (Feb-Mar 2008) from Cape Basin to the northern part of the Weddell Gyre. Cholesterol and brassicasterol were chosen as ideal biomarkers of the heterotrophic and autotrophic carbon pools, respectively, because of their ubiquitous and relatively refractory nature. We document depth distributions of concentrations (relative to bulk POC) and δ13C signatures of cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre combined with CO2 aq. surface concentration variation. While relationships between surface water CO2 aq. and δ13C of bulk POC and biomarkers have been previously established for surface waters, our data show that these remain valid in deeper waters, suggesting that δ13C signatures of certain biomarkers could be developed as proxies for surface water CO2 aq. Our data suggest a key role of zooplankton fecal aggregates in carbon export for this part of the Southern Ocean. We observed a general increase in sterol δ13C signatures with depth, which is likely related to a combination of particle size effects, selective feeding on larger cells by zooplankton, and growth rate related effects Additionally, in the southern part of the transect south of the Polar Front (PF), the release of sea-ice algae is hypothesized to influence the isotopic signature of sterols in the open ocean. Overall, combined use of δ13C and concentrations measurements of both bulk organic C and specific sterol markers throughout the water column shows the promising potential of analyzing δ13C signatures of individual marine sterols to explore the recent history of plankton and the fate of organic matter in the SO

Whole water column distribution and carbon isotopic composition of bulk particulate organic carbon, cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre in the Southern Ocean

International audienceThe combination of concentrations and δ13C signatures of Particulate Organic Carbon (POC) and sterols provides a powerful approach to study ecological and environmental changes both in the modern and ancient ocean, but its application has so far been restricted to the surface area. We applied this tool to study the biogeochemical changes in the modern ocean water column during the BONUS-GoodHope survey (Feb-Mar 2008) from Cape Basin to the northern part of the Weddell Gyre. Cholesterol and brassicasterol were chosen as ideal biomarkers of the heterotrophic and autotrophic carbon pools, respectively, because of their ubiquitous and relatively refractory nature. We document depth distributions of concentrations (relative to bulk POC) and δ13C signatures of cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre combined with CO2 aq. surface concentration variation. While relationships between surface water CO2 aq. and δ13C of bulk POC and biomarkers have been previously established for surface waters, our data show that these remain valid in deeper waters, suggesting that δ13C signatures of certain biomarkers could be developed as proxies for surface water CO2 aq. Our data suggest a key role of zooplankton fecal aggregates in carbon export for this part of the Southern Ocean. We observed a general increase in sterol δ13C signatures with depth, which is likely related to a combination of particle size effects, selective feeding on larger cells by zooplankton, and growth rate related effects Additionally, in the southern part of the transect south of the Polar Front (PF), the release of sea-ice algae is hypothesized to influence the isotopic signature of sterols in the open ocean. Overall, combined use of δ13C and concentrations measurements of both bulk organic C and specific sterol markers throughout the water column shows the promising potential of analyzing δ13C signatures of individual marine sterols to explore the recent history of plankton and the fate of organic matter in the SO