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.
The particulate organic carbon flux from the photic zone provides the major food supply to the seafloor community1 and is an important mechanism of atmospheric CO2 drawdown but usually less than 1% of primary produced organic carbon reaches abyssal depths2. However, excess density by incorporation of ballast minerals (biominerals and lithogenic material) can significantly increase the sinking speed of fresh organic matter and magnitude of carbon export2,3,4,5. Thus, mineral ballasting plays an important role in strengthening the biological carbon pump that transfers particulate organic carbon (POC) from the surface to the deep ocean6. Ballasting by lithogenic material plays a minor role in the deep Central Arctic Ocean6,7,8 and the scarce sediment-trap data available indicate that mineral ballasting of organic carbon in the ice-covered Arctic Ocean is three orders of magnitude lower than the global average6. The resulting POC flux to depths >1000 m in the ice-covered Arctic Ocean is usually 0.17–1 gC m−2yr−1 (refs9,10) (Supplementary Table S1), and is considered to be amongst the lowest in the global ocean6. Even so, infrequently efficient carbon export events have been observed that were associated with the release of ice algal aggregates10,11. These notable exceptions highlight the importance of fast-sinking particles for POC export12 in the Central Arctic.
Concurrent with the transformation of the Arctic sea ice from a thick, multi-year to a thinner, first-year ice cover, recent observations have detected phytoplankton blooms beneath snow-covered sea ice early in the season13 and below ponded ice during the melt period14. The fate of these under-ice blooms is unknown but their occurrence suggests that there is more organic material available for ice-associated mineral ballasting under the new sea ice regime. The recent increase in Phaeocystis under-ice13 and marginal ice zone15,16,17 blooms in the European Arctic could have a negative impact on the strength of the biological carbon pump since Phaeocystis is thought to contribute less to deep carbon export than diatoms18. Whether further seasonal and spatial shifts in primary production and alterations in the phytoplankton community composition will influence POC export in the ice-covered Arctic Ocean is still an open question19,20,21.
The precipitation of gypsum (CaSO4 · H2O) has recently been reported in Arctic sea ice22, but this mineral has never been implicated as a potential ballasting material for POC. Here, we report cryogenic gypsum ballasting of an under-ice phytoplankton bloom dominated by the haptophyte Phaeocystis north of Svalbard: this is the first report of cryogenic gypsum ballasting.
In the spring of 2015, the international “Transitions in the Arctic Seasonal Sea Ice Zone” (TRANSSIZ) expedition of RV Polarstern (PS92, ARK-XXIX/1, 19 May–26 June) systematically investigated the sea-ice ecosystem north of Spitsbergen (Fig. 1)23. At Ice Station PS92/47 (81°22′N, 13°36′E, 2146 m; Fig. 1), which was occupied on June 19 and 20, a multicorer (MUC) with eight tubes was used to retrieve sea-floor surface sediment samples. Simultaneously, a video camera mounted on the MUC frame recorded marine snow aggregates throughout the two hours for both the down- and upcast and, while on the sea floor, those that had already settled (Fig. 2a,b, Supplementary Video S1 and Supplementary Fig. S1).
To understand the origin and composition of the marine snow, aggregates from the sediment surface and, subsequently, from the water column at site PS92/47 were collected and investigated. Larger marine snow aggregates were pipetted from the sediment surface of the MUC tubes (Fig. 2a–b) and like sediments of the topmost surface centimetre stored in a Rose Bengal–ethanol solution24. In the home laboratory, all samples were washed with tap water over a 63-µm mesh sieve, dried, and examined under a stereo microscope.
The >63-µm residue of the Rose Bengal–ethanol-treated algal aggregates (see methods for details) showed remains of Phaeocystis colonies and abundant needle-like crystals: the crystals amounted to half of the aggregate volume (Fig. 2c–d). No biominerals (e.g., planktonic foraminifera, diatom frustules), faecal pellets or terrigenous material were observed in the >63-µm residue (Fig. 2c). However, due to the mesh size that was adapted to micropaleontological work, smaller particles may have been missed during microscopic observations. The needle-like crystals, which had a maximum length of 1 mm and a diameter of 30–300 µm, were only observed in the algal aggregate samples treated with Rose Bengal–ethanol, with none found in the surrounding sediments. No crystals were detected in unpreserved aggregates (stored only in seawater). Thus, for future studies, it is important to note that gypsum crystals were preserved only in ethanol-fixed samples.
To confirm that the Phaeocystis aggregates on the sediment surface had settled through the water column, plankton (>55-µm) and aggregates from the water column (in the upper 2000 m) were collected during two Multi Plankton Sampler (MultiNet) casts (see method). Microscopic analyses of the Rose Bengal–ethanol treated, washed, and dried residues confirmed that remains of Phaeocystis aggregates with embedded crystals occurred in samples from all water depths. However, quantification of the relative aggregate/crystal number and volume was hampered by the sampling technique itself. The use of MultiNets could have allowed re-aggregation of gypsum crystals and aggregates, as well as loss of an unknown quantity of thin needle-like crystals through the nets. Nevertheless, the finding of needle-like crystals entangled in algal aggregates caught with the MultiNets supports the observation of an export event occurring during the video recording and very recent sedimentation of the algal aggregates retrieved from the seafloor.
The crystals retrieved from the aggregates were identified as gypsum by means of confocal Raman microscopy (see Supplementary Fig. S2). The isotopic signature of the gypsum crystals (δ34S = +21.3‰) was consistent with the enrichment expected for abiotic gypsum precipitation from a marine sulphate source (typically δ34S = +20.3‰ ± 0.8‰)25. This observation indicates that the gypsum crystals were precipitated from marine sulphate within sea ice rather than from oxidation of reduced sulphur in biogenic pyrite or organic matter within the algal aggregates, which would have yielded lower δ34S values (−50‰ to +15‰)26,27,28,29.
To estimate the amount of gypsum in the local sea ice, we reconstructed its thermal history and applied FREZCHEM, a chemical–thermodynamic model that was explicitly developed to quantify aqueous electrolyte properties at sub-zero temperatures; it calculates the precipitation of solids by solving the equations of thermodynamic equilibrium using the Pitzer approach30,31. We used FREZCHEM to calculate mineral precipitation in high-salinity brines, and found that gypsum can be precipitated between −6.5° and −8.5 °C and below −18 °C (ref.30) (Fig. 3). Temperatures in first-year Arctic sea ice never reach as low as −18 °C; thus, only the narrow ‘warmer’ precipitation range is of interest in this study. Our model calculations indicate that up to 2.7 g gypsum m−2 could be precipitated. This value is comparable to the observed Phaeocystis (1.6 g C m−2) and POC (9.4 g m−2) standing stocks at Station PS92/47 (Supplementary Table S2) and to standing stocks found during the contemporaneous Norwegian young sea ICE (N-ICE2015) expedition that operated in the vicinity of the current study (average 1.3 g Phaeocystis C m−2, average 11.1 g POC m−2; Supplementary Table S2). The ballasting of POC (here Phaeocystis carbon) with 50% gypsum would increase the density from ~1 to 1.65 g cm−3 with gypsum ballasting. This density increase could enhance the amount and speed of surface-derived organic carbon export to the abyssal ocean32.
The thermodynamic FREZCHEM30 model does not account for the time scales of gypsum dissolution outside the stability range. The direct observation of gypsum crystals at a depth of more than 2 km presented here indicates that the relatively large gypsum crystals observed were stable enough to survive the descent through the water column. Even so, our current knowledge of the kinetics of gypsum dissolution under the conditions at the sampling site is insufficient to exclude the possibility that some smaller crystals dissolved during the descent. Gypsum crystals might have been expelled from the sea ice during warming, even before melting, when brine pockets interconnect at T > −5 °C (ref.33), which is near the warm gypsum precipitation window. The release of crystals to the water column coincided with a large Phaeocystis bloom (Supplementary Fig. S3) that developed beneath the dense pack ice (1.4 m modal sea ice thickness), despite the heavy snow cover (0.4 m modal snow thickness), 80 km north of the marginal ice zone (Fig. 1). The under-ice bloom was facilitated by light transmission through leads in the ice pack and could be observed for one month, from 25 May until 22 June13.
We report here for the first time on the ballasting of a Phaeocystis bloom by cryogenic gypsum released from melting sea ice and thus representing a previously unknown role of this mineral in enhancing deep carbon export in ice covered areas of the world ocean.
The genus Phaeocystis is a common member of the phytoplankton community in the marginal sea-ice zone15,34. Phaeocystis is associated with the inflow of Atlantic water into the Arctic Ocean16,34. It is assumed that the higher temperature of the Atlantic water promotes blooms dominated by Phaeocystis in the eastern Fram Strait34,35. The ability of Phaeocystis to bloom under low and changing light conditions36 enables this organism to take advantage of the occurrence of leads opening up between ice floes13. The combination of a relatively shallow mixed layer (Supplementary Fig. S3) and an occasional light supply through the leads allows Phaeocystis to bloom relatively early and far north (north of 81°N)13.
Although Phaeocystis has been found in surface sediments in the Southern Ocean37, it has been proposed that this alga is remineralized within the upper 50–100 m (refs38,39). However Phaeocystis export events have recently been observed below 300 m at the ice edge in the Arctic Ocean17,40, but they were not related to a release of gypsum crystals and thus did not demonstrate the ballasting export mechanism presented here. Phaeocystis can form large blooms in its colonial stage36. In Phaeocystis colonies (which reach sizes of up to 2 mm), the cells are embedded in a matrix of polysaccharides – they are known to excrete large amounts of mucopolysaccharides and heteropolysaccharides36. This combination of large size and the sticky polysaccharide gel matrix38,39,41 make Phaeocystis colonies in the water column an ideal trap for gypsum crystals released from sea ice. Our video recording of the MUC deployment and aggregate accumulation on the sea floor clearly indicates downward flux of the gypsum-ballasted Phaeocystis (Fig. 2 and Supplementary Data Video S1). Given the timing of the bloom in the study area13, we infer that this process occurred within a relatively short time.
Backtracking the ice floe42 beneath which we observed the Phaeocystis export event, we calculate that gypsum crystals must have formed between December 2014 and February 2015 at temperatures below −6.5 °C. The gypsum crystals would have been released shortly before our sampling operations. This scenario is supported by the simultaneous occurrence of sea-ice temperatures above −5 °C (ref.23, fig. 7.2.2), abundant particles in the water column, and gypsum-ballasted algal aggregates at the sediment surface at a depth of 2146 m, as observed at station PS92/47 (Fig. 2, Supplementary Video S1 and Supplementary Fig. S1). Temperature-induced increase in the brine-channel size and connectivity potentially facilitated the release of gypsum crystals into the water column, coincident with the presence of a similar mass per area of Phaeocystis.
To illustrate the effect of this potential ballasting on carbon drawdown from the surface, we estimated the potential maximum carbon drawdown by Phaeocystis using the integrated net primary production (NPP) for the upper 50 m at station PS92/47. The total NPP was 0.24 ± 0.02 g C m−2 d−1, with a Phaeocystis contribution of 56% (estimated via the share of total phytoplankton carbon standing stock) corresponding to a daily production share of 0.13 ± 0.02 g C m−2 d−1 (Supplementary Table S2). Based on a bloom duration of at least 28 days13, the estimated Phaeocystis NPP amounted to a total of 3.8 ± 0.2 g C m−2 (Supplementary Table 2). Although no shallow carbon export was measured in this study, a purely speculative carbon export of only a quarter of the above-estimated Phaeocystis NPP (approximately 1 g C m−2) to the seafloor during the short-term gypsum ballasting export event would rival the annual carbon export in various deep-sea regions of the Arctic Ocean (Supplementary Table S1). This is in accordance with previous observations that rapid ballasted-particle export can be extremely efficient over very short time scales12.
Given the ongoing changes in the prevailing ice type (thin, first-year sea ice replacing thicker multi-year ice)19, the annual release of cryogenic gypsum may increase in the future. The apparent increase of Phaeocystis blooms in the European Arctic16, the prevalence of under-ice phytoplankton blooms13,14, and the rapid melting of gypsum-containing sea ice could strengthen the export of phytoplankton, particularly Phaeocystis. With the anticipated increase in Arctic primary production43, this ballasting process could lead to an increase in the food supply for abyssal organisms. This change in carbon export efficiency from the surface ocean could impact the structure and functioning of benthic ecosystems, and subsequently alter the cycling of carbon and other biogenic elements, especially in the ice-covered Arctic Ocean. However, this hypothesis still has to be tested in future studies and will require a dedicated observational programme that includes targeted sampling of sea ice and the surface mixed layer, as well as deployments of free-floating sediment traps at various depths for extended time periods.
Unless stated otherwise, all treatments, measurements and analyses were carried out at the Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung in Bremerhaven, Germany.
A multicorer (MUC) with eight tubes of 10-cm inner diameter was used for retrieving undisturbed sea-floor surface sediment samples. Simultaneously, a Sanyo HD400P video camera (10× optical zoom, autofocus, 330 kbit s−1) mounted to the MUC frame routinely recorded the descent and ascent of the MUC (Supplementary Video S1 and Supplementary Fig. 1).
As we had no idea that we would encounter cryogenic gypsum our sampling strategy and applied methods followed the micropaleontological protocol for benthic foraminifera investigations.
Larger marine snow aggregates approximately 1 cm in diameter were pipetted from the sediment surface of three of the MUC tubes selected at random (Fig. 2a,b). The aggregates were transferred into a container with a sample-equivalent volume of Rose Bengal–ethanol solution24. Hereby, ethanol hampers the disintegration of organic matter and gypsum, Rose Bengal stains proteins of early aggregate invaders like foraminifers. In addition, the topmost surface centimetre of each of the three selected MUC tubes was similarly preserved.
Multi plankton sampler
A Midi Hydro-Bios MultiNet, Kiel, Germany (MultiNet), with five nets, each with an opening of 50 × 50 cm, a length of 250 cm and a 55-µm mesh was used for plankton sampling. At station PS92/47 the water column was sampled above 100, 200, 600, 1000 and 2000 m water depths at a speed of 1 m s−1.
Treatment of aggregate and MultiNet samples
In the home laboratory, all samples were washed with tap water over a 63-µm mesh sieve, dried at room temperature (MUC samples) or 50 °C (MultiNet samples), and examined under a stereo microscope (100–160× optical magnification).
For pigment analysis with high pressure liquid chromatography (HPLC), seawater samples (1–2 L) were taken with Niskin bottles from seven depths in the upper 100 m attached to a rosette water sampler with a package of electronic instruments (SBE911plus) that continuously measures conductivity, temperature, and depth (CTD). The sample handling and pigment measurement processing were carried out as described in Kilias et al.44. The taxonomic structure of the phytoplankton groups was calculated from marker pigment ratios using the CHEMTAX program45. Pigment ratios were constrained as suggested by Higgins et al.46 based on microscopic examination of representative samples during the cruise, and the input matrix published by Fragoso et al.47 was applied. The resulting Phaeocystis contribution represents a percentage of the total chlorophyll a (Chl a) biomass and is expressed as µg Chl a L−1. The standing stocks of Phaeocystis, in terms of carbon biomass, were calculated by multiplying the chlorophyll concentrations with a conversion factor of 31.4, which was estimated for this bloom by Assmy et al.13.
Microscopic analyses of phytoplankton
To verify the HPLC pigment measurements, the phytoplankton taxonomic composition was analysed by light microscopy in samples from the chlorophyll maximum (shown for station PS92/47 in Supplementary Fig. 3d). Seawater samples were preserved in hexamethylenetetramine-buffered formalin (final concentration 0.5%) and stored in amber glass bottles. For the microscopic analyses, 50-mL aliquots were transferred to settling chambers where the phytoplankton cells were allowed to settle for 48 h. At least 500 cells of the dominant phytoplankton species or groups were counted with an inverted microscope48 using phase contrast and at three different magnifications. Phytoplankton cells were identified to the genus level, and the phytoplankton carbon content was obtained by multiplying the counts by the carbon values for individual cells. The phytoplankton carbon content was calculated as described in Edler49.
To calculate photosynthetic parameters, seawater samples from the Niskin bottles were incubated at different light levels in the presence of 14C-labelled sodium bicarbonate using the method after Lewis and Smith50. To calculate the integrated primary production, the photosynthetically available radiation (PAR) just below the sea ice was derived from the incoming global radiation measured every 10 minutes over a period of 24 hours by the Polarstern weather station. Hourly PAR values were then estimated by integrating the measurements taken during each hour (n = 6). For each hour, the PAR at different depths (2.1, 5.0, 10.0, 15.0, 30.0, and 50.0 m) was estimated using a 4% transmittance through snow and sea ice, as determined from radiometric measurements taken by a remotely operated vehicle (ROV) and the attenuation coefficient (kdPAR) of 0.15 m−1, which was estimated from vertical light profiles measured during the time at ice station PS92/47.
The hourly primary production at each depth was then estimated using fitted photosynthetic parameters that were derived from photosynthesis versus irradiance (P/I) curves by fitting the model of Platt et al.51 in order to account for photoinhibition. The non-linear fitting was done using the Levenberg–Marquardt algorithm from the minpack.lm R package52.
At each depth, primary production was estimated using photosynthetic-parameter and PAR estimates. Finally, daily primary production (PP) was calculated by integrating production over time and depth. For error estimation of PP, a Monte Carlo procedure was used to propagate the uncertainty of the fitted photosynthetic parameters on the estimated daily primary production. At each depth, a total of 10,000 simulations (i.e., P/I curves) were performed by randomly sampling parameter values based on a multivariate normal distribution of the fitted parameters. Using the generated curves, the depth and daily integrated primary production rates were calculated as described above. The standard deviation of the 10,000 integrated daily primary production rates was then used as a measure of the uncertainty around the estimated value of primary production.
Seawater samples for suspended POC were collected from eight discrete depths between 0 and 200 m, with Niskin bottles mounted on a rosette water sampler with a CTD system (SBE911plus). Triplicate samples (300–500 mL depending on concentration) were filtered onto glass microfiber filters (GF/F) filters (Whatman), precombusted at 500 °C, and immediately frozen at −20 °C for laboratory analysis at UiT, the Arctic University of Norway, Tromsø, which occurred within 6 months of sample collection. For analysis, the frozen filters were dried at 60 °C for 24 h and subsequently placed in an acid fume bath (concentrated hydrochloric acid) for 24 h to remove all inorganic carbon. The filters were then placed into a 60 °C desiccator for an additional 24 h and finally put into nickel capsules for analysis. The samples were analysed for POC using an Exeter Analytical CE440 CHN elemental analyser.
Single crystals were measured with a confocal Raman microscope (WITec alpha 300 R) using an excitation wavelength of 488 nm (pinhole size: 50 µm) and a 20× (Zeiss EC Epiplan, Numerical Aperture = 0.4) lens. This type of instrument is ideal for unambiguous determination of the mineral phase of small (few µm) crystals53,54. As seen from the Raman spectrum (Supplementary Fig. 2), the crystals extracted from the MUC sample yield an exact match to the gypsum in-house standard when measured under identical conditions.
The sulphur isotopic composition (δ43S) of the gypsum extracted from the MUC samples was measured in the Godwin Laboratory at the University of Cambridge (United Kingdom). Gypsum microcrystals (~300 mg) were handpicked and combusted in a tin capsule in the presence of V2O5 at 1030 °C by a Flash Elemental Analyser (Flash EA, Thermo Scientific). The sulphur dioxide produced was measured by continuous-flow gas source isotope ratio mass spectrometry (Thermo Scientific, Delta V Plus). The sample run was bracketed by three standards (NBS-127; +20.3‰). A blank (no sample) was analysed before and after the gypsum sample and the block of standards, to avoid a memory effect. No drift was detected during the run. The reproducibility of the method was better than 0.1‰ (1 sd) based on the analysis of the six NBS-127 standards. All δ43S values are relative to V-CDT (Vienna-Canyon Diablo Troilite). Consistent with Thode et al.55 and Pierre56, the sulphur isotope value (δ43S) of +21.3‰ determined for the gypsum is regarded as indicating a marine source of sulphur (+20.3‰), with an offset of approximately 1‰ due to fractionation during precipitation.
Weight and volume of gypsum in Phaeocystis aggregates
The weight of the gypsum crystals was calculated from a 3-mL volume of algal aggregates pipetted from the MUC sediment surface that was stored in the Rose Bengal–ethanol solution. In the laboratory, the 3-mL sample of algal aggregates was sieved through a 63-µm mesh screen, and the residue was dried at room temperature. All gypsum crystals were picked from this residue, and the weight was determined with a high-precision Sartorius SE2 ultra-microbalance. Using a density value of 2.32 g cm−3, gypsum comprised approximately half of the algal aggregate by volume (>600 µg mL−1).
The incorporation of gypsum in the Phaeocystis aggregates increased the mass density due to ballasting, i.e., 50% (by volume) Phaeocystis (density φ ~ 1) plus 50% gypsum (density φ = 2.3) is equivalent to φ~1.65 g cm−3.
Calculation of potential gypsum precipitation
To evaluate the potential for gypsum precipitation in sea ice and quantify the amount of precipitated crystals, we combined ice-floe backtracking, reanalysis forcing data, a thermodynamic sea-ice model and a geochemical freezing chemistry model. Although each of the individual models has shortcomings and uncertainties, we are confident that we achieved the best possible, conservative estimate of precipitated gypsum mass. Solid precipitation in sea ice is mostly driven by temperature evolution. To reconstruct gypsum growth, we reconstructed ice temperatures of the surveyed area over the winter season before sampling. As no ice-mass-balance buoy was within a reasonable distance during period before sampling, ice temperatures were reconstructed using a thermodynamic model forced by reanalysis data. To assess the correct location of the surveyed ice floe throughout the winter, we used a Lagrangian backtracking algorithm employing a variety of sea-ice drift products42. This process provided a trajectory of the surveyed ice parcel from its initial formation to the location where it was sampled. This trajectory was used to extract the appropriate temperature and six-hourly meteorological forcing data from the European Centre for Medium-Range Weather Forecasts (ECMWF) ERA-Interim reanalysis product57. Together with the assumption of a constant ocean heat flux of 5 W m−2, these data were used to force the SNOWPACK thermodynamic model58,59,60 in a newly developed variant SNOWPACK SeaIce Branch model (http://models.slf.ch/p/snowpack/) to derive the ice growth and the internal temperature field. The total ice thickness of 95 cm (sea ice plus superimposed ice/snow ice) calculated by the model is in good agreement with the modal ice thickness of 90–100 cm measured by electromagnetic induction sounding (GEM2, Geophex, Canada) that was provided in the expedition report23. The fact that the modelled and observed ice thicknesses correspond well strongly suggests that this approach is suitable for reconstruction of the thermodynamic evolution of the ice parcel, despite all the uncertainties involved in backtracking and reanalysis data42.
To calculate the potential for gypsum precipitation, we used the FREZCHEM freezing chemistry model30. This model is frequently used for calculations of seawater freezing, and is thus the best tool for an absolute estimate of total precipitated gypsum mass. Seawater freezing was calculated at 0.1 °C intervals for standard seawater, starting at 0 °C. As the precipitation kinetics of gypsum are largely unknown, especially at low temperatures, we had to base our calculations on two assumptions: first, the fact that we found sea-ice-precipitated gypsum in algal aggregates on the deep-sea floor proves that, once they have formed, gypsum crystals remain stable during the melting phase of sea ice. Hence, once gypsum is produced, it will not be dissolved by further thermal changes in the ice cover. Second, we assume that gypsum precipitation occurs immediately when the temperature threshold is reached. As almost nothing is known about the kinetics of gypsum formation, and the FREZCHEM model does not offer a temporal dimension, this is the only suitable assumption. Earlier observations22 that gypsum crystals form within a limited time frame support the validity of this assumption.
By adding the maximal gypsum formation potentials of all modelled horizontal layers, we estimated the potential gypsum precipitation on our surveyed ice parcel. To account for brine rejection during sea-ice formation, the final precipitated gypsum masses (of 18.8 g gypsum m−2) were divided by the ratio of the seawater salinity of approximately 35 and the observed sea-ice bulk salinity of 5. This results in an estimate of potential gypsum precipitation to 2.7 g gypsum m−2.
Overall, our salinity-corrected estimate likely provides an underestimation, as gypsum precipitation was observed by Geilfus et al.22 within a much wider temperature window, starting at temperatures as high as −3 °C. Higher temperature windows for gypsum precipitation can be easily achieved in FREZCHEM simulations with minor changes to the initial ion composition of the seawater. Additionally, the reanalysis data tend to overestimate snow accumulation on Arctic sea ice, as a significant amount of snow is lost in open leads during snow drift events. Thus, ice temperatures low enough for gypsum precipitation might be present in an even larger portion of the sea-ice column.
Ocean Data View (ODV)
The data shown in Supplementary Fig. 3 were plotted with the Ocean Data View software61. The stations included in the sections are outlined by the red rectangle in the map (c). The plot for Phaeocystis (a) is based on the samples from discrete depths in the upper 50 m (see pigment analysis section) and is gridded with the weighted average method in ODV. The temperature (a, b) and salinity (b) contours are based on CTD sensor data23 with 1-m vertical resolution and are gridded with the DIVA method in ODV.
Jones, D. O. B. et al. Global reductions in seafloor biomass in response to climate change. Glob. Change Biol. 20(6), 1861–1872 (2014).
De La Rocha, C. & Passow, U. Factors influencing the sinking of POC and the efficiency of the biological carbon pump. Deep-Sea Res. II 54(5-7), 639–658 (2007).
Armstrong, R. A., Lee, C., Hedges, J. I., Honjo, S. & Wakeham, S. G. A new, mechanistic model for organic carbon fluxes in the ocean based on the quantitative association of POC with ballast minerals. Deep-Sea Res. II 49(1–3), 219–236 (2002).
Le Moigne, F., Pabortsava, K., Marcinko, C., Martin, P. & Sanders, R. Where is mineral ballast important for surface export of particulate organic carbon in the ocean? Geophys. Res. Letter 41(23), 8460–8468 (2014).
Klaas, C. & Archer, D. E. Association of sinking organic matter with various types of mineral ballast in the deep sea: implications for the rain ratio. Global Biogeochem. Cycles 16, 1–14 (2002).
Honjo, S., Manganini, S. J., Krishfield, R. A. & Francois, R. Particulate organic carbon fluxes to the ocean interior and factors controlling the biological pump: a synthesis of global sediment trap programs since 1983. Prog. Oceanogr. 76, 217–285 (2008).
Fahl, K. & Nöthig, E. M. Lithogenic and biogenic particle fluxes on the Lomonosov Ridge (central Arctic Ocean) and their relevance for sediment accumulation: Vertical vs. lateral transport. Deep Sea Research I 54(8), 1256–1272 (2007).
Honjo, S. et al. Biological pump processes in the cryopelagic and hemipelagic Arctic Ocean: Canada Basin and Chukchi Rise. Prog. Oceanogr. 85, 137–170 (2010).
Harada, N. Review: Potential catastrophic reduction of sea ice in the western Arctic Ocean: Its impact on biogeochemical cycles and marine ecosystems. Glob. Planet. Change 136, 1–17 (2016).
Roca-Martí, M. et al. Carbon export fluxes and export efficiency in the central Arctic during the record sea-ice minimum in 2012: a joint 234Th/238U and 210Po/210Pb study. J. Geophys. Res. Oceans 121, https://doi.org/10.1002/2016JC011816 (2016).
Boetius, A. et al. Export of algal biomass from the melting Arctic sea ice. Science 339, 1430–1432 (2013).
Riley, J. S. et al. The relative contribution of fast and slow sinking particles to ocean carbon export. Glob. Biogeochem. Cycl. 26(GB1026), https://doi.org/10.1029/2011GB004085 (2011).
Assmy, P. et al. Leads in Arctic pack ice enable early phytoplankton blooms below snow-covered sea ice. Sci. Rep. 7, 40850, https://doi.org/10.1038/srep40850 (2017).
Arrigo, K. R. et al. Massive phytoplankton blooms under Arctic sea ice. Science 336, 1408 (2012).
Lasternas, S. & Agusti, S. Phytoplankton community structure during the record Arctic ice-melting of summer 2007. Polar Biol. 33, 1709–1717 (2010).
Nöthig, E.-M. et al. Summertime plankton ecology in Fram Strait - a compilation of long- and short-term observations. Polar Res. 34, https://doi.org/10.3402/polar.v34.23349 (2015).
Moigne Le, F. A. C. et al. Carbon export efficiency and phytoplankton community composition in the Atlantic sector of the Arctic Ocean. J. Geophys. Res. Oceans 120, 3896–3912 (2015).
Reigstad, M. & Wassmann, P. Does Phaeocystis spp. contribute significantly to vertical export of organic carbon? Biogeochemistry 83, 217–234 (2007).
Meier, W. N. et al. Arctic sea ice in transformation: A review of recent observed changes and impacts on biology and human activity. Rev. Geophys. 51, 185–217 (2014).
Lalande, C. et al. Variability in under-ice export fluxes of biogenic matter in the Arctic Ocean. Glob. Biogeochem. Cycl. 28, 571–583 (2014).
Anderson, L. G. & Macdonald, R. W. Observing the Arctic Ocean carbon cycle in a changing environment. Polar Research 34, 26891, https://doi.org/10.3402/polar.v34.26891 (2015).
Geilfus, N. X. et al. Gypsum crystals observed in experimental and natural sea ice. Geophys. Res. Lett. 40, 6362–6367 (2013).
Peeken, I. The Expedition PS92 of the Research Vessel POLARSTERN to the Arctic Ocean in 2015. Rep. Polar Mar. Res. 694, 155, 10013/epic.46750.d001 (2016).
Schönfeld, J. et al. The FOBIMO (FOraminiferal BIo-MOnitoring) initiative—Towards a standardised protocol for soft-bottom benthic foraminiferal monitoring studies. Mar. Micropal. 94-95, 1–13 (2012).
Raab, M. & Spiro, B. Sulfur isotopic variations during seawater evaporation with fractional crystallization. Chem. Geol. 86, 323–333 (1991).
Rees, C. E., Jenkins, W. J. & Monster, J. The sulphur isotopic composition of ocean water sulphate. Geochim. Cosmochim. Acta 42(4), 377–381 (1978).
Paris, G., Sessions, A. L., Subhas, A. V. & Adkins, J. F. MC-ICP-MS measurement of δ34S and Δ33S in small amounts of dissolved sulfate. Chem. Geol. 345, 50–61 (2013).
Strauss, H. The isotopic composition of sedimentary sulfur through time. Palaeogeogr. Palaeoclimatol. Palaeoecol. 132(1–4), 97–118 (1997).
Werne, J. P., Lyons, T. W., Hollander, D. J., Formolo, M. & Sinninghe- Damsté, J. S. Reduced sulfur in euxinic sediments of the Cariaco Basin: Sulfur isotope constraints on organic sulfur formation. Chem. Geol. 195, 159–179 (2003).
Marion, G. M. & Grant, S. A. FREZCHEM: A chemical-thermodynamic model for aqueous solutions at subzero temperatures, CRREL Spec. Rep. 94-18, 1–35 (1994).
Marion, G. M., Mironenko, M. V. & Roberts, M. W. FREZCHEM: A geochemical model for cold aqueous solutions. Comput. Geosci. 36(1), 10–15 (2010).
Sanders, R. et al. Does a ballast effect occur in the surface ocean? Geophys. Res. Lett. 37, L08602, https://doi.org/10.1029/2010GL042574 (2010).
Golden, K. M., Ackley, S. F. & Lytle, V. I. The percolation phase transition in sea ice. Science 282, 2238–2241 (1998).
Degerlund, M. & Eilertsen, H. C. Main species characteristics of phytoplankton spring blooms in NE Atlantic and Arctic waters (68–80°N). Estuaries Coast 33, 242–269 (2010).
Metfies, K., von Appen, W.-J., Kilias, E., Nicolaus, A. & Nöthig, E.-M. Biogeography and photosynthetic biomass of Arctic marine pico-eukaryotes during summer of the record sea ice minimum 2012. PLoS ONE 11, e0148512, https://doi.org/10.1371/journal.pone.0148512 (2016).
Schoemann, W., Becquevort, S., Stefels, J., Rousseau, W. & Lancelot, C. Phaeocystis blooms in the global ocean and their controlling mechanisms: a review. J. Sea Res. 53, 43–66 (2005).
DiTullio, G. R. et al. Rapid and early export of Phaeocystis antarctica blooms in the Ross Sea, Antarctica. Nature 404, 595–598 (2000).
Passow, U. & Wassmann, P. On the trophic fate of Phaeocystis pouchetii (Hariot): IV. The formation of marine snow by. P. pouchetii, Mar. Ecol. Progr. Ser. 104, 153–161 (1994).
Riebesell, U., Reigstad, M., Wassmann, P., Noji, T. & Passow, U. On the trophic fate of Phaeocystis pouchetii (Hariot): VI. Significance of Phaeocystis-derived mucus for vertical flux. Neth. J. Sea Res. 33, 193–203 (1995).
Lalande, C., Bauerfeind, E. & Nöthig, E.-M. Downward particulate organic carbon export at high temporal resolution in the eastern Fram Strait: influence of Atlantic Water on flux composition. Mar. Ecol. Prog. Ser. 440, 127–136 (2011).
Alderkamp, A. C., Buma, A. G. & Van Rijssel, J. M. The carbohydrates of Phaeocystis and their degradation in the microbial food web. Biogeochemistry 83, 99–118 (2007).
Krumpen et al. Recent summer sea ice thickness surveys in Fram Strait and associated ice volume fluxes. The Cryosphere 10, 523–534 (2016).
Randelhoff, A. & Guthrie, J. D. Regional patterns in current and future export production in the central Arctic Ocean quantified from nitrate fluxes. Geophys. Res. Lett. 43, 8600–8608 (2016).
Kilias, E., Wolf, C., Nöthig, E.-M., Peeken, I. & Metfies, K. Protist distribution in the western Fram Strait in Summer 2010 based on 454-Pyrosequencing of 18S RDNA. J. Phycol. 49, 996–1010 (2013).
Mackey, M., Mackey, D., Higgins, H. & Wright, S. CHEMTAX® - a program for estimating class abundances from chemical markers: application to HPLC measurements of phytoplankton. Mar. Ecol. Progr. Ser. 144, 265–283 (1996).
Higgins, H. W., Wright, S. W. & Schlüter, L. Quantitative interpretation of chemotaxonomic pigment data, in Phytoplankton Pigments. Characterization, Chemotaxonomy and Applications in Oceanography (eds Roy, S., Llewellyn, C., Egeland, E. S. & Johnsen, G.) 257–313, Cambridge University Press, Cambridge (2011).
Fragoso, G. M., Poulton, A. J., Yashayaev, I. M., Head, E. J. H. & Purdie, D. A. Spring phytoplankton communities of the Labrador Sea (2000–2014): pigment signatures, photophysiology and elemental ratios, Biogeosciences Discuss. https://doi.org/10.5194/bg-2016-295 (2016).
Utermöhl, H. Zur Vervollkommnung der quantitativen Phytoplankton-Methodik. Mitt. int. Ver. theor. angew. Limnol. 9, 1–38 (1958).
Edler, L. Recommendations on methods for marine biological studies in the Baltic Sea. Phytoplankton and chlorophyll, Publication-Baltic Marine Biologists BMB (Sweden), 38pp (1979).
Lewis, M. R. & Smith, J. C. A. Small volume, short-incubation-time method for measurement of photosynthesis as a function of incident irradiance. Mar. Ecol. Progr. Ser. 13, 99–102 (1983).
Platt, T., Gallegos, C. L. & Harrison, W. G. Photoinhibition of photosynthesis in natural assemblages of marine-phytoplankton. J. Mar. Res. 38, 687–701 (1980).
Elzhov, T. V., Mullen, K. M., Spiess, A.-N. & Bolker, B. R. Interface to the Levenberg- Marquardt nonlinear least-squares algorithm found in MINPACK, plus support for bounds. R package version 1.2-1. https://CRAN.R-project.org/package=minpack.lm. (2016).
Kranz, S. A., Wolf-Gladrow, D., Nehrke, G., Langer, G. & Rost, B. Calcium carbonate precipitation induced by the growth of the marine cyanobacteria Trichodesmium. Limnol. Oceanogr. 55, 2563–2569 (2010).
Hu, Y.-B., Wolthers, M., Wolf-Gladrow, D. A. & Nehrke, G. Effect of pH and phosphate on calcium carbonate polymorphs precipitated at near-freezing temperature. Crystal Growth Design 15, 1596–1601 (2015).
Thode, H. G. & Monster, J. Sulfur isotope geochemistry of petroleum, evaporites and ancient seas. AAPG Memoir 4, 367–377 (1965).
Pierre, C. Isotopic evidence for the dynamic redox cycle of dissolved sulphur compounds between free and interstitial solutions in marine salt pans. Chem. Geol. 53, 191–196 (1985).
Dee, D. P. et al. The ERA-Interim reanalysis: Configuration and performance of the data assimilation system. Quarterly J. Royal Meteorol. Soc. 137, 553–597 (2011).
Lehning, M. et al. SNOWPACK model calculations for avalanche warning based upon a new network of weather and snow stations. Cold Reg. Sci. Technol. 30, 145–157 (1999).
Bartelt, P. & Lehning, M. A physical SNOWPACK model for the Swiss avalanche warning Part I: numerical model. Cold Reg. Sci. Technol. 35, 123–145 (2002).
Wever, N., Fierz, C., Mitterer, C., Hirashima, H. & Lehning, M. Solving Richards Equation for snow improves snowpack meltwater runoff estimations in detailed multi-layer snowpack model. The Cryosphere 8, 257–274 (2014).
Schlitzer, R. Ocean Data View, http://odv.awi.de (2016).
This study used samples and data provided by the Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung in Bremerhaven (Grant No. AWI-PS92_00). We thank the IASC Network ART (Arctic in Rapid Transition) for initiating RV Polarstern expedition PS92 (TRANSSIZ). We thank Philippe Massicotte for his support with the NPP calculation and Yannick Huot for his support of the P/I experiments. We thank the captain and crew for their support at sea. This study was funded by the PACES (Polar Regions and Coasts in a Changing Earth System) Program of the Helmholtz Association. P.A. was supported by the Centre for Ice, Climate and Ecosystems (ICE) at the Norwegian Polar Institute and the Research Council of Norway (project no. 244646).
The authors declare no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Wollenburg, J.E., Katlein, C., Nehrke, G. et al. Ballasting by cryogenic gypsum enhances carbon export in a Phaeocystis under-ice bloom. Sci Rep 8, 7703 (2018). https://doi.org/10.1038/s41598-018-26016-0
This article is cited by
Nature Communications (2023)
Nature Reviews Earth & Environment (2022)
Marine snow morphology illuminates the evolution of phytoplankton blooms and determines their subsequent vertical export
Nature Communications (2021)
Nature Climate Change (2020)
Diversity and Composition of Pelagic Prokaryotic and Protist Communities in a Thin Arctic Sea-Ice Regime
Microbial Ecology (2019)