The carbon cycle of the seasonally ice covered region of the southwest Indian Ocean sector of East Antarctica (30°–80°E, 60°–69°S) was investigated during austral summer (January–March 2006). Large variability in the drivers and timing of carbon cycling dynamics were observed and indicated that the study site was a weak net source of carbon dioxide (CO2) to the atmosphere of 0.8 ± 1.6 g C m−2 during the ice‐free period, with narrow bands of CO2 uptake observed near the continental margin and north of the Southern Antarctic Circumpolar Current Front. Continuous surface measurements of dissolved oxygen and the fugacity of CO2 were combined with net community production estimates from oxygen/argon ratios to show that surface heat gain and photosynthesis were responsible for the majority of observed surface water variability. On seasonal timescales, winter sea‐ice cover reduced the flux of CO2 to the atmosphere in the study area, followed by biologically driven drawdown of CO2 as the ice retreated in spring‐summer highlighting the important role that sea‐ice formation and retreat has on the biogeochemical cycling of the region.
Although the supply of iron generally limits phytoplankton productivity in the Southern Ocean, substantial seasonal blooms are observed over and downstream of the Kerguelen plateau in the Indian sector of the Southern Ocean. Surprisingly, of the oceanic blooms, those associated with the deeper southern plateau last much longer (~3 months) than the northern bloom (~1‐month downstream of northern plateau). In this study, iron supply mechanisms around the southern plateau were investigated, obtaining profiles of dissolved iron (<0.2 μm, dFe) to 2,000‐m deep at 25 stations during austral summer 2016. The dFe concentrations in surface waters (≤100‐m depth) ranged from below the detection limit (DL, median of 0.026 nmol/kg) to 0.34 nmol/kg near the Antarctic shelf, with almost half the data points below detection. These low and—with few exceptions—largely spatially invariant concentrations, presumably driven by seasonal drawdown of this essential micronutrient by phytoplankton, could not explain observed patterns in chlorophyll a. In contrast, dFe concentrations (0.05–1.27 nmol/kg) in subsurface waters (100–800 m) showed strong spatial variations that can explain bloom patterns around the southern Kerguelen plateau when considered in the context of frontal locations and associated frontal processes, including upwelling, that may increase the upward supply of dFe in the region. This sustained vertical dFe supply distinguishes the southern blooms from the bloom downstream of the northern Kerguelen plateau and explains their persistence through the season.
Free-ocean CO2 enrichment (FOCE) experiments have been deployed in marine ecosystems to manipulate carbonate system conditions to those predicted in future oceans. We investigated whether the pH/carbonate chemistry of extremely cold polar waters can be manipulated in an ecologically relevant way, to represent conditions under future atmospheric CO2 levels, in an in-situ FOCE experiment in Antarctica. We examined spatial and temporal variation in local ambient carbonate chemistry at hourly intervals at two sites between December and February and compared these with experimental conditions. We successfully maintained a mean pH offset in acidified benthic chambers of −0.38 (±0.07) from ambient for approximately 8 weeks. Local diel and seasonal fluctuations in ambient pH were duplicated in the FOCE system. Large temporal variability in acidified chambers resulted from system stoppages. The mean pH, Ωarag and fCO2 values in the acidified chambers were 7.688 ± 0.079, 0.62 ± 0.13 and 912 ± 150 µatm, respectively. Variation in ambient pH appeared to be mainly driven by salinity and biological production and ranged from 8.019 to 8.192 with significant spatio-temporal variation. This experiment demonstrates the utility of FOCE systems to create conditions expected in future oceans that represent ecologically relevant variation, even under polar conditions.
<p>Water isotopes measured in ice cores are well-known tracers of paleoclimate variations. The ratio of heavy to light isotope in snow is indeed strongly controlled by the temperature during condensation along the entire airmass transport. This allows the utilization of isotope variability in the water cycle in current climatic conditions, and on weather time scales, to try to pinpoint key events and processes building up (or re-stating) the isotope signature of a given air mass. Because isotopic fractionation occurs every time water changes phase, it is highly beneficial to sample concurrently the different water reservoirs (i.e. seawater, sea ice, snow, rain and vapor) in order to truly understand the processes at work.</p><p>Here we present stable water isotope data from two cruises north of Svalbard within the INTAROS project (summer 2018 and summer 2019). During these cruises, vapor isotope composition was measured quasi-continuously on the coast guard icebreaker <em>KV Svalbard</em>. Seawater and precipitation samples were collected continuously throughout the cruises. The 2018 cruise mainly targeted locations within the Marginal Ice Zone north of Svalbard. On the 2019 cruise, sea ice samples and snow samples were collected at 8 ice stations, all the way to the North Pole. The liquid/solid samples were later analyzed at FARLAB at the University of Bergen.</p><p>A first analysis of the dataset shows that stable water isotope values vary with air mass origin, with marked differences between '<sup>18</sup>O-enriched&#8217; air coming from the south-east (Barents Sea) and &#8216;<sup>18</sup>O-depleted&#8217; air from the north-west (Inner Arctic) during the second cruise. During the 2019 cruise, vapor in air from the south-east tends to have relatively low d-excess values whereas precipitation is largely at equilibrium with the ambient vapor. This INTAROS dataset will be highly beneficial for studies using (coupled) isotope-enabled models, such as earth system models or high-latitude regional climate models, to validate their representation of the high-latitude water cycle.</p><p>&#160;</p>
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