Search

In this article, we analyze the impacts of climate change on Antarctic marine ecosystems. Observations demonstrate large-scale changes in the physical variables and circulation of the Southern Ocean driven by warming, stratospheric ozone depletion, and a positive Southern Annular Mode. Alterations in the physical environment are driving change through all levels of Antarctic marine food webs, which differ regionally. The distributions of key species, such as Antarctic krill, are also changing. Differential responses among predators reflect differences in species ecology. The impacts of climate change on Antarctic biodiversity will likely vary for different communities and depend on species range. Coastal communities and those of sub-Antarctic islands, especially range-restricted endemic communities, will likely suffer the greatest negative consequences of climate change. Simultaneously, ecosystem services in the Southern Ocean will likely increase. Such decoupling of ecosystem services and endemic species will require consideration in the management of human activities such as fishing in Antarctic marine ecosystems. Expected final online publication date for the Annual Review of Marine Science Volume 12 is January 3, 2020. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

Macrozooplankton and its grazing pressure shape ecosystem structures and carbon pathways in the Southern Ocean. Here, we present the implementation of “polar macrozooplankton” as a plankton functional type and a related fast-sinking detritus class (fecal pellets) into the biogeochemical model REcoM-2. We use the model to assess major carbon pathways and ecosystem structure in the Southern Ocean south of 50°S. The model represents zooplankton biomass and its spatial distribution in the Southern Ocean reasonably well in comparison to available biomass data. A distinct difference of our model from previous versions is the seasonal pattern of particle formation processes and ecosystem structures in the Southern Ocean. REcoM-2 now captures high zooplankton biomass and a typical shift from a dominance of phytodetrital aggregates in spring to zooplankton fecal pellets later in the year. At sites with high biomass of macrozooplankton, the transfer efficiency of particulate organic carbon can be as high as 50%, and the carbon content of the exported material increases. In our simulations, macrozooplankton is an important component of the Southern Ocean plankton community, contributing up to 0.12 Pg C per year (14%) to total modeled carbon export across 100 m depth. Macrozooplankton changes the phytoplankton composition and supports the recycling of macronutrients. These results support the important role of macrozooplankton such as krill in the Southern Ocean and have implications for the representation of Southern Ocean biogeochemical cycles in models.

Successful management and mitigation of marine challenges depends on cooperation and knowledge sharing which often occurs across culturally diverse geographic regions. Global ocean science collaboration is therefore essential for developing global solutions. Building effective global research networks that can enable collaboration also need to ensure inter- and transdisciplinary research approaches to tackle complex marine socio-ecological challenges. To understand the contribution of interdisciplinary global research networks to solving these complex challenges, we use the Integrated Marine Biosphere Research (IMBeR) project as a case study. We investigated the diversity and characteristics of 1,827 scientists from 11 global regions who were attendees at different IMBeR global science engagement opportunities since 2009. We also determined the role of social science engagement in natural science based regional programmes (using key informants) and identified the potential for enhanced collaboration in the future. Event attendees were predominantly from western Europe, North America, and East Asia. But overall, in the global network, there was growing participation by females, students and early career researchers, and social scientists, thus assisting in moving toward interdisciplinarity in IMBeR research. The mainly natural science oriented regional programmes showed mixed success in engaging and collaborating with social scientists. This was mostly attributed to the largely natural science (i.e., biological, physical) goals and agendas of the programmes, and the lack of institutional support and push to initiate connections with social science. Recognising that social science research may not be relevant to all the aims and activities of all regional programmes, all researchers however, recognised the (potential) benefits of interdisciplinarity, which included broadening scientists’ understanding and perspectives, developing connections and interlinkages, and making science more useful. Pathways to achieve progress in regional programmes fell into four groups: specific funding, events to come together, within-programme-reflections, and social science champions. Future research programmes should have a strategic plan to be truly interdisciplinary, engaging natural and social sciences, as well as aiding early career professionals to actively engage in such programmes.

A quantitative analysis of any environment older than the instrumental record relies on proxies. Uncertainties associated with proxy reconstructions are often underestimated, which can lead to artificial conflict between different proxies, and between data and models. In this paper, using ordinary least squares linear regression as a common example, we describe a simple, robust and generalizable method for quantifying uncertainty in proxy reconstructions. We highlight the primary controls on the magnitude of uncertainty, and compare this simple estimate to equivalent estimates from Bayesian, nonparametric and fiducial statistical frameworks. We discuss when it may be possible to reduce uncertainties, and conclude that the unexplained variance in the calibration must always feature in the uncertainty in the reconstruction. This directs future research toward explaining as much of the variance in the calibration data as possible. We also advocate for a “data-forward” approach, that clearly decouples the presentation of proxy data from plausible environmental inferences.

Cell division of the coccolithophore Emiliania huxleyi and other phytoplankton typically becomes entrained to diel light/dark cycles under laboratory conditions, with division occurring primarily during dark phases and production occurring during light phases. Under these conditions, increases in cell and biomass concentrations deviate from exponential functions on time scales < 24 h. These deviations lead to significant diel variations in common measurements of phytoplankton physiology such as cellular quotas of particulate organic and inorganic carbon (POC, PIC) and their production rates. Being time-dependent, only the temporal mean of the various values during the day are comparable between experiments. Deviations from exponential growth furthermore imply that increases in cell and biomass concentrations cannot be expressed by the daily growth rate μ_{24 h} (typically determined from daily increments in cell concentrations). Consequently, conventional calculations of production as the product of a cellular quota (e.g., POC quota) and μ_{24 h} are mathematically incorrect. To account for this, we here describe short-term changes in cell and biomass concentrations of fastdividing, dilute-batch cultures of E. huxleyi grown under a diel light/dark cycle using linear regression. Based on the derived models, we present calculations for daily means of cellular quotas and production rates. Conventional (time-specific) measurements of cellular quotas and production differ from daily means by up to 65% in our example and, under some circumstances, cause false “effects” of treatments. Intending to reduce errors in ecophysiological studies, we recommend determining daily means—mathematically or by adjusting the experimental setup or sampling times appropriately.

The genesis of phytoplankton blooms and the fate of their biomass in iron-limited, high-nutrient−low-chlorophyll regions can be studied under natural conditions with ocean iron fertilization (OIF) experiments. The Indo-German OIF experiment LOHAFEX was carried out over 40 d in late summer 2009 within the cold core of a mesoscale eddy in the productive southwest Atlantic sector of the Southern Ocean. Silicate concentrations were very low, and phytoplankton biomass was dominated by autotrophic nanoflagellates (ANF) in the size range 3−10 μm. As in all previous OIF experiments, the phytoplankton responded to iron fertilization by increasing the maximum quantum yield (Fv/Fm) and cellular chlorophyll levels. Within 3 wk, chlorophyll levels tripled and ANF biomass doubled. With the exception of some diatoms and dinoflagellates, the biomass levels of all other groups of the phyto- and protozooplankton (heterotrophic nanoflagellates, dinoflagellates and ciliates) remained remarkably stable throughout the experiment both inside and outside the fertilized patch. We attribute the unusually high biomass attained and maintained by ANF to the absence of their grazers, the salps, and to constraints on protozooplankton grazers by heavy predation exerted by the large copepod stock. The resistance to change of the ecosystem structure over 38 d after fertilization, indicated by homogeneity at regional and temporal scales, suggests that it was locked into a stable, mature state that had evolved in the course of the seasonal cycle. The LOHAFEX bloom provides a case study of a resistant/robust dynamic equilibrium between auto- and heterotrophic ecosystem components resulting in low vertical flux both inside and outside the patch despite high biomass levels.

The LOHAFEX iron fertilization experiment was conducted for 39 days in the closed core of a cyclonic mesoscale eddy located along the Antarctic Polar Front in the Atlantic sector of the Southern Ocean. Mixed layer (ML) waters were characterized by high nitrate (~ 20 μM), low dissolved iron (DFe ~ 0.2 nM) and low silicate concentrations (below 1 μM) restricting diatom growth. Upon initial fertilization, chlorophyll-a doubled during the first two weeks and stabilized thereafter, despite a second fertilization on day 21, due to an increase in grazing pressure. Biomass at the different trophic levels was mostly comprised of small autotrophic flagellates, the large copepod Calanus simillimus and the amphipod Themisto gaudichaudii. The downward flux of particulate material comprised mainly copepod fecal pellets that were remineralized in the upper 150 m of the water column with no significant deeper export. DFe concentrations in the upper 200 m were not significantly affected by the two fertilizations but after day 14 showed a greater variability (ranging from 0.3 to 1.3 nM) without a clear vertical pattern. Particulate iron concentrations (measured after 2 months at pH 1.4) decreased with time and showed a vertical pattern that indicated an important non-biogenic component at the bottom of the mixed layer. In order to assess the contribution of copepod grazing to iron cycling we used two different approaches: first, we measured for the first time in a field experiment copepod fecal pellet concentrations in the water column together with the iron content per pellet, and second, we devised a novel analytical scheme based on a two-step leaching protocol to estimate the contribution of copepod fecal pellets to particulate iron in the water column. Analysis of the iron content of isolated fecal pellets from C. simillimus showed that after the second fertilization, the iron content per fecal pellet was ~ 5 fold higher if the copepod had been captured in fertilized waters. We defined a new fraction termed leachable iron (pH 2.0) in 48 h (LFe48h) that, for the conditions during LOHAFEX, was shown to be an excellent proxy for the concentration of iron contained in copepod fecal pellets. We observed that, as a result of the second fertilization, iron accumulated in copepod fecal pellets and remained high at one third of the total iron stock in the upper 80 m. We hypothesize that our observations are due to a combination of two biological processes. First, phagotrophy of iron colloids freshly formed after the second fertilization by the predominant flagellate community resulted in higher Fe:C ratios per cell that, via grazing, lead to iron enrichment in copepod fecal pellets in fertilized waters. Second, copepod coprophagy could explain the rapid recycling of particulate iron in the upper 100–150 m, the accumulation of LFe48h in the upper 80 m after the second fertilization and provided the iron required for the maintenance of the LOHAFEX bloom for many weeks. Our results provide the first quantitative evidence of the major ecological relevance of copepods and their fecal products in the cycling of iron in silicate depleted areas of the Southern Ocean., This work was supported by the Government of Spain (MINECO CTM2008-01864-E/ANT and CTM2014-59244-C3-3-R). LML was supported by the Campus de Excelencia Internacional Program (Ministerio de Educación, Cultura y Deportes, España).

A recent numerical cell model, which explains observed light and carbonate system effects on particulate organic and inorganic carbon (POC and PIC) production rates under the assumption of internal pH homeostasis, is extended for stable carbon isotopes (12C, 13C). Aim of the present study is to mechanistically understand the stable carbon isotopic fractionation signal (e) in POC and PIC and furthermore the vital effect(s) included in measured ePIC values. The virtual cell is divided into four compartments, for each of which the 12C as well as the 13C carbonate system kinetics are implemented. The compartments are connected to each other via trans-membrane fluxes. In contrast to existing carbon fractionation models, the presented model calculates the disequilibrium state for both carbonate systems and for each compartment. It furthermore calculates POC and PIC production rates as well as ePOC and ePIC as a function of given light conditions and the compositions of the external carbonate system. Measured POC and PIC production rates as well as ePIC values are reproduced well by the model (comparison with literature data). The observed light effect on ePOC (increase of ePOC with increasing light intensities), however, is not reproduced by the basic model set-up, which is solely based on RubisCO fractionation. When extending the latter set-up by assuming that biological fractionation includes further carbon fractionation steps besides the one of RubisCO, the observed light effect on ePOC is also reproduced. By means of the extended model version, four different vital effects that superimpose each other in a real cell can be detected. Finally, we discuss potential limitations of the ePIC proxy.

Salp fecal pellets are rich in organic matter and have been shown to sink at very high velocities. In recent years, salp abundances have been increasing in the Southern Ocean where they seem to be replacing krill as the dominant grazers on phytoplankton. As salps can form large swarms with high pellet production rates, it has been suggested that they will become increasingly important for the vertical export of particulate organic matter in the Southern Ocean. However, detailed studies combining both investigations of pellet production rates, turnover, and export are still needed in order to determine whether salp pellets are important for export (‘sinkers’) or recycling (‘floaters’) of organic matter. Our results suggest that pellets are produced at high rates in the upper few hundred meters of the water column. Although we observed high sinking velocities and low microbial degradation rates of the produced salp pellets, only about one third of the produced pellets were captured in sediment traps placed at 100 m and about ~13% of the produced pellets were exported to sediment traps placed at 300 m. The high retention of these fast-settling pellets seems to be caused by break-up and loosening of the pellets, possibly by zooplankton and salps themselves. We measured 3-fold lower size-specific sinking velocities in loosened and fragmented compared to freshly produced intact pellets-. This enhanced the residence times (>1 day) of both small and large pellets in the upper water column. We postulate that the fragile nature of salp pellets make them more important for recycling of organic matter in the upper mesopelagic layer rather than as a conduit for export of particulate organic matter to the seafloor.

International audience; The influence of eddy structures on the seasonal depletion of dissolved inorganic carbon (DIC) and carbon dioxide (CO2) disequilibrium was investigated during a trans-Atlantic crossing of the Antarctic Circumpolar Current (ACC) in austral summer 2012. The Georgia Basin, downstream of the island of South Georgia (54-55°S, 36-38°W) is a highly dynamic region due to the mesoscale activity associated with the flow of the Subantarctic Front (SAF) and Polar Front (PF). Satellite sea-surface height and chlorophyll-a anomalies revealed a cyclonic cold core that dominated the northern Georgia Basin that was formed from a large meander of the PF. Warmer waters influenced by the SAF formed a smaller anticyclonic structure to the east of the basin. Both the cold core and warm core eddy structures were hotspots of carbon uptake relative to the rest of the ACC section during austral summer. This was most amplified in the cold core where greatest CO2 undersaturation (-78 μatm) and substantial surface ocean DIC deficit (5.1 mol m-2) occurred. In the presence of high wind speeds, the cold core eddy acted as a strong sink for atmospheric CO2 of 25.5 mmol m-2 day-1. Waters of the warm core displayed characteristics of the Polar Frontal Zone (PFZ), with warmer upper ocean waters and enhanced CO2 undersaturation (-59 μatm) and depletion of DIC (4.9mol m-2). A proposed mechanism for the enhanced carbon uptake across both eddy structures is based on the Ekman eddy pumping theory: (i) the cold core is seeded with productive (high chlorophyll-a) waters from the Antarctic Zone and sustained biological productivity through upwelled nutrient supply that counteracts DIC inputs from deep waters; (ii) horizontal entrainment of low-DIC surface waters (biological uptake) from the PFZ downwell within the warm core and cause relative DIC-depletion in the upper water column. The observations suggest that the formation and northward propagation of cold core eddies in the region of the PF could project low-DIC waters towards the site of Antarctic Intermediate Water formation and enhance CO2 drawdown into the deep ocean.

Measuring temperature and salinity profiles in the world's oceans is crucial to understanding ocean dynamics and its influence on the heat budget, the water cycle, the marine environment and on our climate. Since 1983 the German research vessel and icebreaker Polarstern has been the platform of numerous CTD (conductivity, temperature, depth instrument) deployments in the Arctic and the Antarctic. We report on a unique data collection spanning 33 years of polar CTD data. In total 131 data sets (1 data set per cruise leg) containing data from 10 063 CTD casts are now freely available at doi:10.1594/PANGAEA.860066. During this long period five CTD types with different characteristics and accuracies have been used. Therefore the instruments and processing procedures (sensor calibration, data validation, etc.) are described in detail. This compilation is special not only with regard to the quantity but also the quality of the data – the latter indicated for each data set using defined quality codes. The complete data collection includes a number of repeated sections for which the quality code can be used to investigate and evaluate long-term changes. Beginning with 2010, the salinity measurements presented here are of the highest quality possible in this field owing to the introduction of the OPTIMARE Precision Salinometer.

The Western Antarctic Peninsula (WAP), one of the most productive regions of the Southern Ocean, is currently undergoing rapid environmental changes such as ocean acidification (OA) and increased daily irradiances from enhanced surface‐water stratification. To assess the potential for future biological CO2 sequestration of this region, we incubated a natural phytoplankton assemblage from Ryder Bay, WAP, under a range of pCO2 levels (180 μatm, 450 μatm, and 1000 μatm) combined with either moderate or high natural solar radiation (MSR: 124 μmol photons m−2 s−1 and HSR: 435 μmol photons m−2 s−1, respectively). The initial and final phytoplankton communities were numerically dominated by the prymnesiophyte Phaeocystis Antarctica, with the single cells initially being predominant and solitary and colonial cells reaching similar high abundances by the end. Only when communities were grown under ambient pCO2 in conjunction with HSR did the small diatom Fragilariopsis pseudonana outcompete P. Antarctica at the end of the experiment. Such positive light‐dependent growth response of the diatom was, however, dampened by OA. These changes in community composition were caused by an enhanced photosensitivity of diatoms, especially F. pseudonana>/i>, under OA and HSR, reducing thereby their competitiveness toward P. Antarctica. Moreover, community primary production (PP) of all treatments yielded similar high rates at the start and the end of the experiment, but with the main contributors shifting from initially large to small cells toward the end. Even though community PP of Ryder Bay phytoplankton was insensitive to the changes in light and CO2 availability, the observed size‐dependent shift in productivity could, however, weaken the biological CO2 sequestration potential of this region in the future.

Mineral ballasting enhances carbon export from the surface to the deep ocean; however, little is known about the role of this process in the ice-covered Arctic Ocean. Here, we propose gypsum ballasting as a new mechanism that likely facilitated enhanced vertical carbon export from an under-ice phytoplankton bloom dominated by the haptophyte Phaeocystis. In the spring 2015 abundant gypsum crystals embedded in Phaeocystis aggregates were collected throughout the water column and on the sea floor at a depth below 2 km. Model predictions supported by isotopic signatures indicate that 2.7 g m−2 gypsum crystals were formed in sea ice at temperatures below −6.5 °C and released into the water column during sea ice melting. Our finding indicates that sea ice derived (cryogenic) gypsum is stable enough to survive export to the deep ocean and serves as an effective ballast mineral. Our findings also suggest a potentially important and previously unknown role of Phaeocystis in deep carbon export due to cryogenic gypsum ballasting. The rapidly changing Arctic sea ice regime might favour this gypsum gravity chute with potential consequences for carbon export and food partitioning between pelagic and benthic ecosystems.

Harde (2017) proposes an alternative accounting scheme for the modern carbon cycle and concludes that only 4.3% of today's atmospheric CO2 is a result of anthropogenic emissions. As we will show, this alternative scheme is too simple, is based on invalid assumptions, and does not address many of the key processes involved in the global carbon cycle that are important on the timescale of interest. Harde (2017) therefore reaches an incorrect conclusion about the role of anthropogenic CO2 emissions. Harde (2017) tries to explain changes in atmospheric CO2 concentration with a single equation, while the most simple model of the carbon cycle must at minimum contain equations of at least two reservoirs (the atmosphere and the surface ocean), which are solved simultaneously. A single equation is fundamentally at odds with basic theory and observations. In the following we will (i) clarify the difference between CO2 atmospheric residence time and adjustment time, (ii) present recently published information about anthropogenic carbon, (iii) present details about the processes that are missing in Harde (2017) , (iv) briefly discuss shortcoming in Harde's generalization to paleo timescales, (v) and comment on deficiencies in some of the literature cited in Harde (2017) .

Antarctic Intermediate Water (AAIW) formation constitutes an important mechanism for the export of macronutrients out of the Southern Ocean that fuels primary production in low latitudes. We used quality-controlled gridded data from five hydrographic cruises between 1990 and 2014 to examine decadal variability in nutrients and dissolved inorganic carbon (DIC) in the AAIW (neutral density range 27 < γ n

In the rapidly changing Arctic Ocean, marine primary productivity is tightly linked to the balance between light and nutrient limitation. To capture this balance in ocean general circulation biogeochemical models (OGCBMs), a good representation of the physics is important due to the tight bio-physical coupling in the Arctic. Using a horizontal model resolution of a few kilometers makes it possible to resolve an increasing number of small scale processes, that otherwise need to be parameterized in OGCBMs. Such high resolution is, however, commonly not possible due to computational constrains. Utilizing an unstructured mesh approach, we have run the finite element sea-ice ocean model (FESOM 1.4) coupled to the biogeochemical model REcoM2 in a global configuration with an Arctic-wide resolution of 4.5 km. This resolution is so far unprecedented for a global biogeochemical setup, and here we present an analysis of the mean state of the model. FESOM-REcoM2’s integrated Arctic net primary production (NPP) averages 445 Tg C yr−1 for the years 2011 to 2015, a value that is in the middle of the range compared to estimates from the literature. Most production takes place in the inflow regions of the Nordic and Chukchi Seas, and 32% is associated with the sea ice zone, the latter including the marginal ice zone and below-ice productivity. Light limits production to some degree at all latitudes north of 60°N, with growth becoming nutrient limited following the initial spring bloom in most places. The model reproduces the relatively low surface concentration of dissolved inorganic nitrogen (DIN) that has been observed in the central Arctic Ocean, as well as the low surface DIN concentration towards the end of the growth season further to the south, thereby also capturing widespread subsurface chlorophyll maxima (SCM). The SCMs are found in the whole Arctic except for the areas where sea ice concentration is high the whole year. They have a duration of two weeks to five months. The balance between nutrient and light limitations, both in the vertical and horizontal direction, highlights that decreased light limitation in a future ice free Arctic Ocean will not necessarily induce an increase in NPP due to increasing nutrient limitation, and that further studies of the role of the SCMs are required.

Increasing concern about the impacts of climate change on ecosystems is prompting ecologists and ecosystem managers to seek reliable projections of physical drivers of change. The use of global climate models in ecology is growing, although drawing ecologically meaningful conclusions can be problematic. The expertise required to access and interpret output from climate and earth system models is hampering progress in utilizing them most effectively to determine the wider implications of climate change. To address this issue, we present a joint approach between climate scientists and ecologists that explores key challenges and opportunities for progress. As an exemplar, our focus is the Southern Ocean, notable for significant change with global implications, and on sea ice, given its crucial role in this dynamic ecosystem. We combined perspectives to evaluate the representation of sea ice in global climate models. With an emphasis on ecologically-relevant criteria (sea ice extent and seasonality) we selected a subset of eight models that reliably reproduce extant sea ice distributions. While the model subset shows a similar mean change to the full ensemble in sea ice extent (approximately 50% decline in winter and 30% decline in summer), there is a marked reduction in the range. This improved the precision of projected future sea ice distributions by approximately one third, and means they are more amenable to ecological interpretation. We conclude that careful multidisciplinary evaluation of climate models, in conjunction with ongoing modeling advances, should form an integral part of utilizing model output.

The rise in anthropogenic CO2 and the associated ocean acidification (OA) will change trace metal solubility and speciation, potentially altering Southern Ocean (SO) phytoplankton productivity and species composition. As iron (Fe) sources are important determinants of Fe bioavailability, we assessed the effect of Fe-laden dust versus inorganic Fe (FeCl3) enrichment under ambient and high pCO2 levels (390 and 900 μatm) in a naturally Fe-limited SO phytoplankton community. Despite similar Fe chemical speciation and net particulate organic carbon (POC) production rates, CO2-dependent species shifts were controlled by Fe sources. Final phytoplankton communities of both control and dust treatments were dominated by the same species, with an OA-dependent shift from the diatom Pseudo nitzschia prolongatoides towards the prymnesiophyte Phaeocystis antarctica. Addition of FeCl3 resulted in high abundances of Nitzschia lecointei and Chaetoceros neogracilis under ambient and high pCO2, respectively. These findings reveal that both the characterization of the phytoplankton community at the species level and the use of natural Fe sources are essential for a realistic projection of the biological carbon pump in the Fe-limited pelagic SO under OA. As dust deposition represents a more realistic scenario for the Fe-limited pelagic SO under OA, unaffected net POC production and dominance of P. antarctica can potentially weaken the export of carbon and silica in the future.

A dominant Antarctic ecological paradigm suggests that winter sea ice is generally the main feeding ground for krill larvae. Observations from our winter cruise to the southwest Atlantic sector of the Southern Ocean contradict this view and present the first evidence that the pack-ice zone is a food-poor habitat for larval development. In contrast, the more open marginal ice zone provides a more favourable food environment for high larval krill growth rates. We found that complex under-ice habitats are, however, vital for larval krill when water column productivity is limited by light, by providing structures that offer protec- tion from predators and to collect organic material released from the ice. The larvae feed on this sparse ice-associated food during the day. After sunset, they migrate into the water below the ice (upper 20 m) and drift away from the ice areas where they have previously fed. Model analyses indicate that this behaviour increases both food uptake in a patchy food environment and the likelihood of overwinter transport to areas where feeding conditions are more favourable in spring.

11 páginas, 6 figuras, 2 tablas.-- C.J.M. Hoppe ... et al.-- Proyecto Carbochange.-- This is an open access article under the CCBY-NC-ND license, The Antarctic Circumpolar Current has a high potential for primary production and carbon sequestration through the biological pump. In the current study, two large-scale blooms observed in 2012 during a cruise with R.V. Polarstern were investigated with respect to phytoplankton standing stocks, primary productivity and nutrient budgets. While net primary productivity was similar in both blooms, chlorophyll a –specific photosynthesis was more efficient in the bloom closer to the island of South Georgia (39 °W, 50 °S) compared to the open ocean bloom further east (12 °W, 51 °S). We did not find evidence for light being the driver of bloom dynamics as chlorophyll standing stocks up to 165 mg m−2 developed despite mixed layers as deep as 90 m. Since the two bloom regions differ in their distance to shelf areas, potential sources of iron vary. Nutrient (nitrate, phosphate, silicate) deficits were similar in both areas despite different bloom ages, but their ratios indicated more pronounced iron limitation at 12 °W compared to 39 °W. While primarily the supply of iron and not the availability of light seemed to control onset and duration of the blooms, higher grazing pressure could have exerted a stronger control toward the declining phase of the blooms, C.J.M.H. and B.R. were funded by the European Research Council (ERC) under the European Community׳s Seventh Framework Programme (FP7/2007-2013), ERC Grant agreement no. 205150. S.T. was funded by the German Science Foundation (DFG), project TR 899/2 and the Helmholtz Impulse Fond (HGF Young Investigator Group EcoTrace). Funding to M.S. was supplied by CAPES, Brazil (Grant BEX 3483/09-6), and to A.B. by the Helmholtz Innovation Fund Phytooptics. This work was funded by the MINECO of Spain (Grant CGL2010-11846-E) and the Government of the Balearic Islands (Grant AAEE083/09). J.S.E. was supported by the JAE-Doc program of the CSIC. M.H. was supported through EU FP7 project CARBOCHANGE, which received funding from the European Community׳s Seventh Framework Programme under Grant agreement no. 264879. This work was furthermore supported by the DFG in the framework of the priority programme "Antarctic Research with comparative investigations in Arctic ice areas" by a Grant HO 4680/1

Phytoplankton community structure and their physiological response in the vicinity of the Antarctic Polar Front (APF; 44°S to 53°S, centred at 10°E) were investigated as part of the ANT-XXVIII/3 Eddy-Pump cruise conducted in austral summer 2012. Our results show that under iron-limited View the MathML source(0.6mgm−3) can be observed at stations with deep mixed layer View the MathML source(>60m) across the APF. In contrast, light was excessive at stations with shallower mixed layer and phytoplankton were producing higher amounts of photoprotective pigments, diadinoxanthin (DD) and diatoxanthin (DT), at the expense of TChl-a, resulting in higher ratios of (DD+DT)/TChl-a. North of the APF, significantly lower silicic acid (Si(OH)4) concentrations View the MathML source(5mmolm−3) region south of the APF, on the contrary, was dominated by microphytoplankton (diatoms and dinoflagellates) with lower ratios of (DD+DT)/TChl-a, despite having been exposed to higher levels of irradiance. The significant correlation between nanophytoplankton and (DD+DT)/TChl-a indicates that differences in taxon-specific response to light are also influencing TChl-a concentration in the APF during summer. Our results reveal that provided mixing is deep and Si(OH)4 is replete, TChl-a concentrations higher than View the MathML source0.6mgm−3 are achievable in the iron-limited APF waters during summer.

The δ13C value measured on benthic foraminiferal tests is widely used by palaeoceanographers to reconstruct the distribution of past water masses. The biogeochemical processes involved in forming the benthic foraminiferal δ13C signal (δ13Cforam), however, are not fully understood and a sound mechanistic description is still lacking. We use a reaction–diffusion model for calcification developed by Wolf-Gladrow et al. (1999) and Zeebe et al. (1999) in order to quantify the effects of different physical, chemical, and biological processes on δ13Cforam of an idealised benthic foraminiferal shell. Changes in the δ13C value of dissolved inorganic carbon (δ13CDIC) cause equal changes in δ13Cforam in the model. The results further indicate that temperature, respiration rate, and pH have a significant impact on δ13Cforam. In contrast, salinity, pressure, the δ13C value of particulate organic carbon (δ13CPOC), total alkalinity, and calcification rate show only a limited influence. In sensitivity experiments we assess how combining these effects can influence δ13Cforam. We can potentially explain 33 to 47% of the interglacial-to-glacial decrease in δ13Cforam by changes in temperature and pH, without invoking changes in δ13CDIC. Furthermore, about a quarter of the − 0.4‰ change in δ13Cforam observed in phytodetritus layers can be accounted for by an increase in respiration rate and a reduction in pH.

Stratospheric ozone depletion and emission of greenhouse gases lead to a trend of the Southern Annular Mode (SAM) towards its high-index polarity. The positive phase of the SAM is characterised by stronger than usual westerly winds that induce changes in the physical carbon transport. Changes in the natural carbon budget of the upper 100 m of the Southern Ocean in response to a positive SAM phase are explored with a coupled ecosystem-general circulation model and regression analysis. Previously overlooked processes that are important for the upper ocean carbon budget during a positive SAM period are identified, namely export production and downward transport of carbon north of the Polar Front (PF) as large as the upwelling in the south. The limiting micronutrient iron is brought into the surface layer by upwelling and stimulates phytoplankton growth and export production, but only in summer. This leads to a drawdown of carbon and less summertime outgassing (or more uptake) of natural CO2. In winter, biological mechanisms are inactive and the surface ocean equilibrates with the atmosphere by releasing CO2. In the annual mean, the upper ocean region south of the PF loses more carbon by additional export production than by the release of CO2 into the atmosphere, highlighting the role of the biological carbon pump in response to a positive SAM event.

Chemical weathering is an integral part of both the rock and carbon cycles and is being affected by changes in land use, particularly as a result of agricultural practices such as tilling, mineral fertilization, or liming to adjust soil pH. These human activities have already altered the terrestrial chemical cycles and land-ocean flux of major elements, although the extent remains difficult to quantify. When deployed on a grand scale, Enhanced Weathering (a form of mineral fertilization), the application of finely ground minerals over the land surface, could be used to remove CO2 from the atmosphere. The release of cations during the dissolution of such silicate minerals would convert dissolved CO2 to bicarbonate, increasing the alkalinity and pH of natural waters. Some products of mineral dissolution would precipitate in soils or be taken up by ecosystems, but a significant portion would be transported to the coastal zone and the open ocean, where the increase in alkalinity would partially counteract "ocean acidification" associated with the current marked increase in atmospheric CO2. Other elements released during this mineral dissolution, like Si, P, or K, could stimulate biological productivity, further helping to remove CO2 from the atmosphere. On land, the terrestrial carbon pool would likely increase in response to Enhanced Weathering in areas where ecosystem growth rates are currently limited by one of the nutrients that would be released during mineral dissolution. In the ocean, the biological carbon pumps (which export organic matter and CaCO3 to the deep ocean)may be altered by the resulting influx of nutrients and alkalinity to the ocean. This review merges current interdisciplinary knowledge about Enhanced Weathering, the processes involved, and the applicability aswell as some of the consequences and risks of applying the method.

In the early 1980s, Germany started a new era of modern Antarctic research. The Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research (AWI) was founded and important research platforms such as the German permanent station in Antarctica, today called Neumayer III, and the research icebreaker Polarstern were installed. The research primarily focused on the Atlantic sector of the Southern Ocean. In parallel, the German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) started a priority program ‘Antarctic Research’ (since 2003 called SPP-1158) to foster and intensify the cooperation between scientists from different German universities and the AWI as well as other institutes involved in polar research. Here, we review the main findings in meteorology and oceanography of the last decade, funded by the priority program. The paper presents field observations and modelling efforts, extending from the stratosphere to the deep ocean. The research spans a large range of temporal and spatial scales, including the interaction of both climate components. In particular, radiative processes, the interaction of the changing ozone layer with large-scale atmospheric circulations, and changes in the sea ice cover are discussed. Climate and weather forecast models provide an insight into the water cycle and the climate change signals associated with synoptic cyclones. Investigations of the atmospheric boundary layer focus on the interaction between atmosphere, sea ice and ocean in the vicinity of polynyas and leads. The chapters dedicated to polar oceanography review the interaction between the ocean and ice shelves with regard to the freshwater input and discuss the changes in water mass characteristics, ventilation and formation rates, crucial for the deepest limb of the global, climate-relevant meridional overturning circulation. They also highlight the associated storage of anthropogenic carbon as well as the cycling of carbon, nutrients and trace metals in the ocean with special emphasis on the Weddell Sea. DFG/SPP/1158

Hunt J.R., George L. ... et al.-- 42 pages, 11 figures, We compare and contrast the ecological impacts of atmospheric and oceanic circulation patterns on polar and sub-polar marine ecosystems. Circulation patterns differ strikingly between the north and south. Meridional circulation in the north provides connections between the sub-Arctic and Arctic despite the presence of encircling continental landmasses, whereas annular circulation patterns in the south tend to isolate Antarctic surface waters from those in the north. These differences influence fundamental aspects of the polar ecosystems from the amount, thickness and duration of sea ice, to the types of organisms, and the ecology of zooplankton, fish, seabirds and marine mammals. Meridional flows in both the North Pacific and the North Atlantic oceans transport heat, nutrients, and plankton northward into the Chukchi Sea, the Barents Sea, and the seas off the west coast of Greenland. In the North Atlantic, the advected heat warms the waters of the southern Barents Sea and, with advected nutrients and plankton, supports immense biomasses of fish, seabirds and marine mammals. On the Pacific side of the Arctic, cold waters flowing northward across the northern Bering and Chukchi seas during winter and spring limit the ability of boreal fish species to take advantage of high seasonal production there. Southward flow of cold Arctic waters into sub-Arctic regions of the North Atlantic occurs mainly through Fram Strait with less through the Barents Sea and the Canadian Archipelago. In the Pacific, the transport of Arctic waters and plankton southward through Bering Strait is minimal. In the Southern Ocean, the Antarctic Circumpolar Current and its associated fronts are barriers to the southward dispersal of plankton and pelagic fishes from sub-Antarctic waters, with the consequent evolution of Antarctic zooplankton and fish species largely occurring in isolation from those to the north. The Antarctic Circumpolar Current also disperses biota throughout the Southern Ocean, and as a result, the biota tends to be similar within a given broad latitudinal band. South of the Southern Boundary of the ACC, there is a large-scale divergence that brings nutrient-rich water to the surface. This divergence, along with more localized upwelling regions and deep vertical convection in winter, generates elevated nutrient levels throughout the Antarctic at the end of austral winter. However, such elevated nutrient levels do not support elevated phytoplankton productivity through the entire Southern Ocean, as iron concentrations are rapidly removed to limiting levels by spring blooms in deep waters. However, coastal regions, with the upward mixing of iron, maintain greatly enhanced rates of production, especially in coastal polynyas. In these coastal areas, elevated primary production supports large biomasses of zooplankton, fish, seabirds, and mammals. As climate warming affects these advective processes and their heat content, there will likely be major changes in the distribution and abundance of polar biota, in particular the biota dependent on sea ice.

Carbon dioxide removal (CDR) approaches are efforts to reduce the atmospheric CO2 concentration. Here we use a marine carbon cycle model to investigate the effects of one CDR technique: the open ocean dissolution of the iron-containing mineral olivine. We analyse the maximum CDR potential of an annual dissolution of 3 Pg olivine during the 21st century and focus on the role of the micro-nutrient iron for the biological carbon pump. Distributing the products of olivine dissolution (bicarbonate, silicic acid, iron) uniformly in the global surface ocean has a maximum CDR potential of 0.57 gC/g-olivine mainly due to the alkalinisation of the ocean, with a significant contribution from the fertilisation of phytoplankton with silicic acid and iron. The part of the CDR caused by ocean fertilisation is not permanent, while the CO2 sequestered by alkalinisation would be stored in the ocean as long as alkalinity is not removed from the system. For high CO2 emission scenarios the CDR potential due to the alkalinity input becomes more efficient over time with increasing ocean acidification. The alkalinity-induced CDR potential scales linearly with the amount of olivine, while the iron-induced CDR saturates at 113 PgC per century (on average ~1.1 PgC yr−1) for an iron input rate of 2.3 Tg Fe yr−1 (1% of the iron contained in 3 Pg olivine). The additional iron-related CO2 uptake occurs in the Southern Ocean and in the iron-limited regions of the Pacific. Effects of this approach on surface ocean pH are small (< 0.01).

The Southern Ocean supports diverse and unique ecosystems that have been impacted by more than two centuries of exploitation and are now experiencing rapid changes in ocean temperature and seasonal ice cover due to climate warming. Understanding and projecting responses of Southern Ocean marine ecosystems to changing climate conditions and direct human impacts, such as fisheries, requires integrated ecosystem analyses at scales previously unexplored. Here we consider the main ecological and modelling challenges in predicting the responses of Southern Ocean ecosystems to change, and propose three interlinked focus areas that will advance the development of integrated models for Southern Ocean ecosystems. The first focus area is development of fundamental understanding of the factors that determine the structure and function of the food webs at multiple scales. Ecological research in the Southern Ocean is often centred on key species or localised systems, a tendency which is reflected in existing food web and ecosystem models. To build on this, a systematic analysis of regional food web structure and function is required. The second focus area is development of a range of mechanistic models that vary in their resolution of ecological processes, and consider links across physical scales, biogeochemical cycles and feedbacks, and the central role of zooplankton. These two focus areas underlie the third, which is development of methodologies for scenario testing across a range of trophic levels of the effects of past and future changes, which will facilitate consideration of the underlying complexity of interactions and the associated uncertainty. The complex nature of interactions determining Southern Ocean ecosystem structure and function will require new approaches, which we propose should be developed within a scale-based framework that emphasises both physical and ecological aspects.

The growing field of ocean acidification research is concerned with the investigation of organism responses to increasing pCO2 values. One important approach in this context is culture work using seawater with adjusted CO2 levels. As aqueous pCO2 is difficult to measure directly in small-scale experiments, it is generally calculated from two other measured parameters of the carbonate system (often AT, CT or pH). Unfortunately, the overall uncertainties of measured and subsequently calculated values are often unknown. Especially under high pCO2, this can become a severe problem with respect to the interpretation of physiological and ecological data. In the few datasets from ocean acidification research where all three of these parameters were measured, pCO2 values calculated from AT and CT are typically about 30% lower (i.e. ~300 μatm at a target pCO2 of 1000 μatm) than those calculated from AT and pH or CT and pH. This study presents and discusses these discrepancies as well as likely consequences for the ocean acidification community. Until this problem is solved, one has to consider that calculated parameters of the carbonate system (e.g. pCO2, calcite saturation state) may not be comparable between studies, and that this may have important implications for the interpretation of CO2 perturbation experiments.

The low surface nitrate concentration and high atmospheric iron input in the tropical eastern North Atlantic provide beneficial conditions for N-2 fixation. Varying abundances of diazotrophs have been observed and an Fe- and P-colimitation of N-2 fixation was reported in this ocean region. It is however unclear, how different limiting factors control the temporal variability of N-2 fixation and what the role of Fe-limitation is in a region with high fluxes of dust deposition. To study the environmental controls on N-2 fixation, an one-dimensional ecosystem model is coupled with a physical model for the Tropical Eastern North Atlantic Times-series Station (TENATSO), north of the Cape Verde Islands. The model describes diazotrophy according to the physiology of Trichodesmium, taking into account a growth dependence on light, temperature, iron, dissolved inorganic (DIP) and organic phosphorus (DOP). The modelled total Chl a is compared with satellitederived total Chl a and modelled Trichodesmium (Tri) compared with satellite-derived cyanobacterial Chl a as well as with High Performance Liquid Chromatography data. Model results show a complex pattern of competitive as well as mutually beneficial interactions between diazotrophs and non-diazotrophic phytoplankton. High DOP availability after spring blooms of non-diazotrophic phytoplankton and the ability of Trichodesmium to take up DOP are crucial for allowing a maximal abundance of Tri in autumn. Part of the reactive nitrogen newly fixed by diazotrophs is directly excreted or released through mortality, significantly fuelling the growth of non-diazotrophic phytoplankton in autumn and winter. Fe consumption by non-diazotrophic phytoplankton earlier in the year makes Fe limitation of Tri in late summer more acute, whereas Tri growth in surface waters reduces phytoplankton abundance deeper in the water column by light limitation. Overall, the atmospheric iron input at the TENATSO site is required to enable diazotrophic growth and to support the observed abundance of non-diazotrophic phytoplankton

We analyzed 214 new core-top samples for their CaCO3 content from shelves all around Antarctica in order to understand their distribution and contribution to the marine carbon cycle. The distribution of sedimentary CaCO3 on the Antarctic shelves is connected to environmental parameters where we considered water depth, width of the shelf, sea-ice coverage and primary production. While CaCO3 contents of surface sediments are usually low, high (> 15%) CaCO3 contents occur at shallow water depths (150–200 m) on the narrow shelves of the eastern Weddell Sea and at a depth range of 600–900 m on the broader and deeper shelves of the Amundsen, Bellingshausen and western Weddell Seas. Regions with high primary production, such as the Ross Sea and the western Antarctic Peninsula region, have generally low CaCO3 contents in the surface sediments. The predominant mineral phase of CaCO3 on the Antarctic shelves is low-magnesium calcite. With respect to ocean acidification, our findings suggest that dissolution of carbonates in Antarctic shelf sediments may be an important negative feedback only after the onset of calcite undersaturation on the Antarctic shelves. Macrozoobenthic CaCO3 standing stocks do not increase the CaCO3 budget significantly as they are two orders of magnitude lower than the budget of the sediments. This first circumpolar compilation of Antarctic shelf carbonate data does not claim to be complete. Future studies are encouraged and needed to fill data gaps especially in the under-sampled southwest Pacific and Indian Ocean sectors of the Southern Ocean.

We introduce a novel, simple method to measure sinking velocity of particles and aggregates in roller tanks. Using this noninvasive method, it is possible to follow changes in sinking velocities on the same aggregates during time and to make paired measurements of aggregate sinking velocity and composition. Particles and aggregates are video recorded in roller tanks, and their sinking velocity is derived from the orbital trajectories. This new method is compared with three other methods (using roller tanks, a vertical flow system, and a sedimentation column), which have not previously been inter-calibrated. Agar spheres and diatom aggregates were used as model particles in all experimental systems. No method showed significantly different sinking velocities of agar spheres compared with those calculated by theory. Paired measurements showed that sinking velocities from 70 to 700 m d(-1) were linearly correlated between different methods. Highest sinking velocities were measured in a sedimentation column followed by those measured in roller tanks and in the vertical flow system, respectively. The average difference of sinking velocity measured with the different methods ranged from 8% to 11% for agar spheres, and up to 20% for diatom aggregates.

Ongoing acidification of the global ocean necessitates a solid understanding of how biogeochemical processes are driving proton cycling and observed pH changes in natural waters. The standard way of calculating the pH evolution of an aquatic system is to specify first how biogeochemical processes affect total alkalinity, followed by the solution of a nonlinear acid-base equilibrium equation system. This approach, however, does not explicitly reveal how individual biogeochemical processes contribute to the overall proton cycling in the system. Here, we provide an extension of the classical acid-base theory that explicitly quantifies the proton production/ consumption by a given process, showing that it can be calculated as the proton-cycling sensitivity times the rate of the biogeochemical process at hand. The proton-cycling sensitivity emerges as a central concept in acid-base chemistry of natural waters and can be further decomposed as the ratio of a stoichiometric coefficient for the proton over the buffer factor. The stoichiometric coefficient for the proton expresses how many moles of protons would be produced per mole of reaction if buffering was absent, and is obtained by bringing the reaction equation of the process into a specific form: the fractional reaction equation at ambient pH. The buffer factor quantifies how acid-base systems attenuate the proton production/consumption by biogeochemical processes, and is identified as the negative of the partial derivative of the total alkalinity with respect to the proton concentration. Applying this new concept to an acidification scenario for the future surface ocean, we illustrate its potential to analyze proton cycling in natural waters. Thereby we show that a reduced buffer factor due to anthropogenic carbon input makes the ocean more vulnerable to any process influencing the pH.

The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean acidification on marine organisms and communities but few have provided details concerning full carbonate chemistry and complementary observations. Additionally, carbonate system variables are often reported in different units, calculated using different sets of dissociation constants and on different pH scales. Hence the direct comparison of experimental results has been problematic and often misleading. The need was identified to (1) gather data on carbonate chemistry, biological and biogeochemical properties, and other ancillary data from published experimental data, (2) transform the information into common framework, and (3) make data freely available. The present paper is the outcome of an effort to integrate ocean carbonate chemistry data from the literature which has been supported by the European Network of Excellence for Ocean Ecosystems Analysis (EUR-OCEANS) and the European Project on Ocean Acidification (EPOCA). A total of 185 papers were identified, 100 contained enough information to readily compute carbonate chemistry variables, and 81 data sets were archived at PANGAEA – The Publishing Network for Geoscientific & Environmental Data. This data compilation is regularly updated as an ongoing mission of EPOCA. Data access: http://doi.pangaea.de/10.1594/PANGAEA.735138

Despite their microscopic size, marine phytoplankton are responsible for about half of the global primary production and represent the basis of the marine food web. This diverse group of organisms drives important biogeochemical cycles, exporting massive amounts of carbon to deep waters and sediments, and strongly influencing ocean–atmosphere gas exchanges. Anthropogenic climate change will result in significant alterations in the marine environment over the next 100 yr and beyond. The increase in atmospheric CO2 has already caused significantly higher aquatic CO2 concentrations and lower pH values (‘ocean acidification’) than in pre-industrial times. Rising temperatures will also impact surface ocean stratification, which in turn will affect the surface-water light regime and nutrient input from deeper layers. Phytoplankton will be affected by these environmental changes in many ways. In this article we assess the possible responses of different phytoplankton groups with regard to the expected physico-chemical changes. In addition to summarizing laboratory and field studies, we outline the current understanding of the underlying mechanisms that cause processes such as photosynthesis, calcification, and nitrogen fixation to be sensitive to ocean acidification. We describe different approaches to manipulate carbonate chemistry (e.g. acid/base or CO2 addition), discuss their potential to simulate future ocean acidification, and allude to common problems in experiments caused, for instance, by high biomass or the use of buffers. In addition to guidelines for CO2 perturbation experiments, we argue that it is essential to look at multiple environmental factors in combination with CO2, to aim for process-understanding rather than correlation, and to assess a wider diversity of phytoplankton species both in laboratory and field studies.

This paper primarily reviews our recent work on the biology and geochemistry of foraminifera with respect to their use as paleoceanographic proxies. Our approach to proxy validation and development is described, primarily from a modeler’s point of view. The approach is based on complementary steps in understanding the inorganic chemistry, inorganic isotope fractionation, and biological controls that determine paleo-tracer signals in organisms used in climate reconstructions. Integration of laboratory experiments, field and culture studies, theoretical considerations, and numerical modeling holds the key to the method’s success. We describe effects of life-processes in foraminifera on stable carbon, oxygen, and boron isotopes as well as Mg incorporation into foraminiferal calcite shells. Stable boron isotopes will be used to illustrate our approach. We show that a mechanism-based understanding is often required before primary climate signals can be extracted from the geologic record because the signals can be heavily overprinted by secondary, non-climate related phenomena. Moreover, for some of the proxies, fundamental knowledge on the thermodynamic, inorganic basis is still lacking. One example is stable boron isotopes, a paleo-pH proxy, for which the boron isotope fractionation between the dissolved boron compounds in seawater was not precisely known until recently. Attempts to overcome such hurdles are described and implications of our work for paleoceanographic reconstructions are discussed.

International audience; We use a suite of eight ocean biogeochemical/ecological general circulation models from the Marine Ecosystem Model Intercomparison Project and Coupled Model Intercomparison Project Phase 5 archives to explore the relative roles of changes in winds (positive trend of Southern Annular Mode, SAM) and in warming- and freshening-driven trends of upper ocean stratification in altering export production and CO2 uptake in the Southern Ocean at the end of the 21st century. The investigated models simulate a broad range of responses to climate change, with no agreement on a dominance of either the SAM or the warming signal south of 44°S. In the southernmost zone, i.e., south of 58°S, they concur on an increase of biological export production, while between 44 and 58°S the models lack consensus on the sign of change in export. Yet in both regions, the models show an enhanced CO2 uptake during spring and summer. This is due to a larger CO2(aq) drawdown by the same amount of summer export production at a higher Revelle factor at the end of the 21st century. This strongly increases the importance of the biological carbon pump in the entire Southern Ocean. In the temperate zone, between 30 and 44°S, all models show a predominance of the warming signal and a nutrient-driven reduction of export production. As a consequence, the share of the regions south of 44°S to the total uptake of the Southern Ocean south of 30°S is projected to increase at the end of the 21st century from 47 to 66% with a commensurable decrease to the north. Despite this major reorganization of the meridional distribution of the major regions of uptake, the total uptake increases largely in line with the rising atmospheric CO2. Simulations with the MITgcm-REcoM2 model show that this is mostly driven by the strong increase of atmospheric CO2, with the climate-driven changes of natural CO2 exchange offsetting that trend only to a limited degree (∼10%) and with negligible impact of climate effects on anthropogenic CO2 uptake when integrated over a full annual cycle south of 30°S.

The effects of pH and phosphate on the precipitation of calcium carbonate polymorphs from aqueous solution were investigated. Experiments were carried out at near-freezing temperature and two different pH conditions (pH 13.4 and 9.0). At each pH condition, solutions having different concentrations of CaCl2 and NaHCO3 were mixed to achieve Ca/CO3 ratios of 1:1 and 10:1 at different pumping rates with and without phosphate. Results showed that, at pH 13.4, only ikaite was formed, independent of pumping rate, Ca/CO3 ratio, and phosphate. At pH 9.0, the precipitate was predominantly vaterite in the absence of phosphate and ikaite in the presence of phosphate regardless of the ratio of Ca/CO3. These results indicate that at low temperatures and moderate alkaline conditions (pH 9.0), phosphate can act as a switch between ikaite and vaterite polymorphs. Contrastingly, at higher alkaline conditions (pH 13.4) phosphate is not prerequisite and the high pH in itself is enough to trigger ikaite formation over vaterite.

Coccolithophores play a crucial role in the marine carbon cycle and thus it is interesting to know how they will respond to climate change. After several decades of research the interplay between intracellular processes and the marine carbonate system is still not well understood. On the basis of experimental findings given in literature, a numerical cell model is developed that describes inorganic carbon fluxes between seawater and the intracellular sites of calcite precipitation and photosynthetic carbon fixation. The implemented cell model consists of four compartments, for each of which the carbonate system is resolved individually. The four compartments are connected to each other via H+, CO2, and View the MathML sourceHCO3− fluxes across the compartment-confining membranes. For CO2 accumulation around RubisCO, an energy-efficient carbon concentrating mechanism is proposed that relies on diffusive CO2 uptake. At low external CO2 concentrations and high light intensities, CO2 diffusion does not suffice to cover the carbon demand of photosynthesis and an additional uptake of external View the MathML sourceHCO3− becomes essential. The model is constrained by data of Emiliania huxleyi, the numerically most abundant coccolithophore species in the present-day ocean.

Earth System Science has developed over the last two decades from an interesting concept in Earth sciences education to a fully integrative science focussed on understanding the complex system Earth. This evolution is partially due to the radical and far reaching anthropogenic changes and the general feeling of helplessness with regards to the possible consequences and future impacts on the Earth System. This paper proposes that a paradigm shift in undergraduate and graduate education is needed to further develop Earth System Science. Graduate programs such as the Earth System Science Research School (ESSReS), which are intrinsically trans- and interdisciplinary will help to change rigid subject specific mind-set among faculty and students. The health and sustainability of our planet is at stake.

Ikaite (CaCO3�6H2O) has recently been discovered in sea ice, providing first direct evidence of CaCO3 precipitation in sea ice. However, the impact of ikaite precipitation on phosphate (PO4) concentration has not been considered so far. Experiments were set up at pH from 8.5 to 10.0, salinities from 0 to 105, temperatures from 24°C to 0°C, and PO4 concentrations from 5 to 50 mmol kg-1 in artificial sea ice brine so as to understand how ikaite precipitation affects the PO4 concentration in sea ice under different conditions. Our results show that PO4 is coprecipitated with ikaite under all experimental conditions. The amount of PO4 removed by ikaite precipitation increases with increasing pH. Changes in salinity (S >=35) as well as temperature have little impact on PO4 removal by ikaite precipitation. The initial PO4 concentration affects the PO4 coprecipitation. These findings may shed some light on the observed variability of PO4 concentration in sea ice.

y . Dissolved boron in seawater occurs mainly in the form of boric acid B OH and borate B OH . While the 34 equilibrium properties of the dissociation of boric acid have been studied in detail, very little work has focused on the kinetics of the boric acid-borate equilibrium in seawater. Here, we present a theoretical study of the relaxation of the w

Dissolved inorganic carbon in sea water plays a key role in understanding the properties of the oceanic carbon reservoir within the global carbon cycle. For instance, fluxes between the atmosphere and the ocean are estimated using the stable carbon isotopes 12C and 13C of atmospheric CO2 and its dissolved forms within the ocean. Likewise, the investigation of carbon uptake by marine phytoplankton or the reconstruction of past oceans via stable isotope analysis demand a sound understanding of the sea water chemistry and associated carbon isotope fractionation. Chemical and isotopic disequilibrium is of particular interest when small length and time scales are considered. For example, within the microenvironment of marine plankton or within the surface boundary layer of the ocean (gas exchange atmosphere-ocean) the seawater carbonate chemistry deviates appreciably from equilibrium. It can be shown that a time-dependent description of the carbonate system is indispensable when time scales smaller than 90 s are involved (length scale of the diffusive boundary layer ∼10−4 m). Properties of the equilibrium state of the carbonate system in sea water are well known. However, hitherto there is little detailed work on the disequilibrium state of the chemical and in particular on the isotopic properties of the system. Here we present analytical and numerical techniques to determine the relaxation time of the chemical system including νCO2,HνCO−3,νCO2−3, H+, OH−, B(OH)3, and B(OH)4−, where ν=12, 13, and 14. The calculated relaxation time for chemical equilibrium at a temperature of 25°C and a salinity of 35 at pH 8.2 is 15.9 s (only 12C species), while the time calculated for isotopic equilibrium is 17.5 s (all carbon isotopes considered).

The excretion of siderophores and the reduction of organic iron-complexes at the cell surface are common reactions of terrestrial plants, fungi and bacteria in response to low availability of iron. However, there is much less evidence for the use of these strategies by marine phytoplankton. It has been argued that siderophore excretion is inefficient in an aquatic environment due to rapid diffusion. This study examines how diffusion and chemical reactions in the microenvironment of a phytoplankton cell influence the efficiency of both strategies to increase the bioavailability of iron and to reduce iron stress. A numerical model of the cell surroundings is presented that calculates the concentration distribution for different iron species and allows to study the effect of siderophores or surface reductases. It calculates the efficiency of these mechanisms, defined as the quotient between the increase in iron uptake rate and the excretion rate of siderophores or electrons, needed to obtain this increase. The dependence of this efficiency on rates of iron coordination reactions, on diffusivity, and on the kinetics of iron uptake is discussed with the aid of some analytical calculations.

The results of an existing one-dimensional diagnostic model that calculates the fugacity of CO 2 (fCO 2 ) in the surface layer of the southern ocean were compared with in situ observations from different ocean sectors and seasons. Our model is based on the translation of monthly variations of constraints fields into surface water fCO 2 variations, and was used to assess the CO 2 uptake of the southern ocean. In situ observations are useful to verify the model results and were here applied to improve the estimation of the CO 2 uptake of the southern ocean south of 50 S. The model reproduces the fCO 2 distribution in both Pacific and Indian sectors of the southern ocean satisfactorily, the mean deviation being only 5 μatm. This diserepancy requires only a minor modification of the CO 2 uptake calculated by the model for that area. By contrast, the model strongly underestimates the fCO 2 levels in carly spring and early winter in the Weddell gyre. This indicates that the CO 2 uptake by the Atlantic sector of the southern ocean as calculated by the model, amounting to 0.47 GtC yr -1 . should be reduced, possibly by about half of this value. The reason for this mismatch lies in the use of climatological physical constraints by the model, that do not sufficiently well describe reality. Partly, the mismatch is also caused by a difference of seasonal stage between the model which reflects climatological conditions and the real ocean which is affected by interannual variability. Based on this study it is concluded that the CO 2 uptake of the southern ocean south of 50 S is likely to lie somewhere between 0.6 and 0.7 GtC yr -1 for the 1990s, which is a high value compared to estimates from other investigations.

Inorganic carbon uptake by phytoplankton depletes the immediate cell environment and disturbs the carbonate system equilibrium. Uptake is balanced by both diffusional transport across and chemical reactions within the depleted boundary layer. In this study, we have derived a model that simulates inorganic carbon diffusion and reactions in the vicinity of phytoplankton cells. To allow a general application of the model, the reaction kinetics of the carbonate system are reviewed and temperature- and salinity-dependence of the various rate constants are discussed. A consistency condition for some of the kinetic rates is derived. The effective thickness of the diffusive boundary layer in spherical and planar geometry is discussed. In addition, the effect of cell shape on diffusive transport to phytoplankton is examined and a simple means to account for this effect in model calculations is presented. In a second step, the complete description of the diffusion-reaction system is simplified to consider two special cases in which (1) algal production relies on CO2(aq) as the single source of inorganic carbon, and (2) CO2, HCO3−, or CO32− are utilized independently for organic matter production combined with calcite precipitation. In the size range typical for phytoplankton cells model predictions of these simplified versions are nearly identical to those of the complete model, indicating that the simplified models represent good approximations of the complete diffusion-reaction system.

[1] We combined data sets of measured sedimentary calcium carbonate (CaCO3) and satellite-derived pelagic primary production to parameterize the relation between CaCO3 content on the Antarctic shelves and primary production in the overlying water column. CaCO3 content predicted in this way was in good agreement with the measured data. The parameterization was then used to chart CaCO3 content on the Antarctic shelves all around the Antarctic, using the satellite-derived primary production. The total inventory of CaCO3 in the bioturbated layer of Antarctic shelf sediments was estimated to be 0.5 Pg C. This quantity is comparable to the total CO2 uptake by the Southern Ocean in only one to a few years (dependent on the uptake estimate and area considered), indicating that the dissolution of these carbonates will neither delay ocean acidification in this area nor augment the Southern Ocean CO2 uptake capacity.

Assmy, Philipp ... et. al.-- 6 pages, 4 figures, Diatoms of the iron-replete continental margins and North Atlantic are key exporters of organic carbon. In contrast, diatoms of the iron-limited Antarctic Circumpolar Current sequester silicon, but comparatively little carbon, in the underlying deep ocean and sediments. Because the Southern Ocean is the major hub of oceanic nutrient distribution, selective silicon sequestration there limits diatom blooms elsewhere and consequently the biotic carbon sequestration potential of the entire ocean. We investigated this paradox in an in situ iron fertilization experiment by comparing accumulation and sinking of diatom populations inside and outside the iron-fertilized patch over 5 wk. A bloom comprising various thin- and thick-shelled diatom species developed inside the patch despite the presence of large grazer populations. After the third week, most of the thinner-shelled diatom species underwent mass mortality, formed large, mucous aggregates, and sank out en masse (carbon sinkers). In contrast, thicker-shelled species, in particular Fragilariopsis kerguelensis, persisted in the surface layers, sank mainly empty shells continuously, and reduced silicate concentrations to similar levels both inside and outside the patch (silica sinkers). These patterns imply that thick-shelled, hence grazer-protected, diatom species evolved in response to heavy copepod grazing pressure in the presence of an abundant silicate supply. The ecology of these silica-sinking species decouples silicon and carbon cycles in the iron-limited Southern Ocean, whereas carbon- sinking species, when stimulated by iron fertilization, export more carbon per silicon. Our results suggest that large-scale iron fertilization of the silicate-rich Southern Ocean will not change silicon sequestration but will add carbon to the sinking silica flux, P.A. was supported through Deutsche Forschungsgemeinschaft–Cluster of Excellence “The Ocean in the Earth System” and the Centre for Ice, Climate and Ecosystems at the Norwegian Polar Institute