The export flux of particulate organic carbon derived from 210Po∕210Pb disequilibria along the North Atlantic GEOTRACES GA01 transect: GEOVIDE cruise

© The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution 4.0 License. The definitive version was published in Biogeosciences 16(2), (2019): 309-327, doi:10.5194/bg-16-309-2019.The disequilibrium between 210Po activity and 210Pb activity in seawater samples was determined along the GEOTRACES GA01 transect in the North Atlantic during the GEOVIDE cruise (May–June 2014). A steady-state model was used to quantify vertical export of particulate 210Po. Vertical advection was incorporated into one version of the model using time-averaged vertical velocity, which had substantial variance. This resulted in large uncertainties for the 210Po export flux in this model, suggesting that those calculations of 210Po export fluxes should be used with great care. Despite the large uncertainties, there is no question that the deficits of 210Po in the Iberian Basin and at the Greenland Shelf have been strongly affected by vertical advection. Using the export flux of 210Po and the particulate organic carbon (POC) to 210Po ratio of total (> 1 µm) particles, we determined the POC export fluxes along the transect. Both the magnitude and efficiency of the estimated POC export flux from the surface ocean varied spatially within our study region. Export fluxes of POC ranged from negligible to 10 mmol C m−2 d−1, with enhanced POC export in the Labrador Sea. The cruise track was characterized by overall low POC export relative to net primary production (export efficiency < 1 %–15 %), but relatively high export efficiencies were seen in the basins where diatoms dominated the phytoplankton community. The particularly low export efficiencies in the Iberian Basin, on the other hand, were explained by the dominance of smaller phytoplankton, such as cyanobacteria or coccolithophores. POC fluxes estimated from the 210Po∕210Pb and 234Th∕238U disequilibria agreed within a factor of 3 along the transect, with higher POC estimates generally derived from 234Th. The differences were attributed to integration timescales and the history of bloom events.We thank the captain (Gilles Ferrand) and crew of the R/V Pourquoi Pas? and the chief scientists (Geráldine Sarthou and Pascale Lherminier) of the GEOVIDE cruise. We also thank Pierre Branellec, Floriane Desprez de Gésincourt, Michel Hamon, Catherine Kermabon, Philippe Le Bot, Stéphane Leizour, Olivier Ménage, Fabien Pérault, and Emmanuel de Saint-Léger for their technical support during the GEOVIDE expedition; Catherine Schmechtig for the GEOVIDE database management, and Phoebe Lam for providing two modified McLane in situ pumps; Frédéric Planchon, Virginie Sanial, and Catherine Jeandel for their assistance with pump deployments and particulate sample collection. The authors also thank Arnout Roukaerts, Debany Fonseca-Batista, Florian Deman, and Frank Dehairs for providing primary production data. Funding for the GEOVIDE cruise was provided by the French National Research Agency (ANR-13-BS06-0014, ANR-12-PDOC-0025-01), the French National Center for Scientific Research (CNRS-LEFE-CYBER), the LabexMER (anr-10-LABX-19), and Ifremer. Gillian Stewart and Yi Tang were supported by NSF award #OCE 1237108. The Generalitat de Catalunya also helped through its grant 2017 SGR-1588. This work is contributing to the ICTA “Unit of Excellence” (MinECo, MDM2015-0552). Maxi Castrillejo and Montserrat Roca-Marti were funded by an FPU PhD studentship (AP-2012-2901 and AP2010-2510, respectively) from the Ministerio de Educación, Cultura y Deporte of Spain. Maxi Castrillejo was also supported by the ETH Zurich Postdoctoral Fellowship Program (17-2 FEL-30), co-funded by the Marie Curie Actions for People COFUND Program. We also thank Gary Hemming (Queens College) and Troy Rasbury (Stony Brook University) for laboratory assistance with the ICP-MS analyses. Finally, we thank the associate editor and the anonymous reviewers for their helpful comments on how to improve the manuscript

The export flux of particulate organic carbon derived from 210Po/210Pb disequilibria along the North Atlantic GEOTRACES GA01 transect: GEOVIDE cruise

The disequilibrium between 210Po activity and 210Pb activity in seawater samples was determined along the GEOTRACES GA01 transect in the North Atlantic during the GEOVIDE cruise (May-June 2014). A steady-state model was used to quantify vertical export of particulate 210Po. Vertical advection was incorporated into one version of the model using time-averaged vertical velocity, which had substantial variance. This resulted in large uncertainties for the 210Po export flux in this model, suggesting that those calculations of 210Po export fluxes should be used with great care. Despite the large uncertainties, there is no question that the deficits of 210Po in the Iberian Basin and at the Greenland Shelf have been strongly affected by vertical advection. Using the export flux of 210Po and the particulate organic carbon (POC) to 210Po ratio of total (\u3e1μm) particles, we determined the POC export fluxes along the transect. Both the magnitude and efficiency of the estimated POC export flux from the surface ocean varied spatially within our study region. Export fluxes of POC ranged from negligible to 10mmolCm-2d-1, with enhanced POC export in the Labrador Sea. The cruise track was characterized by overall low POC export relative to net primary production (export efficiency \u3c1%-15%), but relatively high export efficiencies were seen in the basins where diatoms dominated the phytoplankton community. The particularly low export efficiencies in the Iberian Basin, on the other hand, were explained by the dominance of smaller phytoplankton, such as cyanobacteria or coccolithophores. POC fluxes estimated from the 210Po210Pb and 234Th238U disequilibria agreed within a factor of 3 along the transect, with higher POC estimates generally derived from 234Th. The differences were attributed to integration timescales and the history of bloom events. © 2019 Author(s)

The export flux of particulate organic carbon derived from 210Po/210Pb disequilibria along the North Atlantic GEOTRACES GA01 transect: GEOVIDE cruise

The disequilibrium between 210Po activity and 210Pb activity in seawater samples was determined along the GEOTRACES GA01 transect in the North Atlantic during the GEOVIDE cruise (May-June 2014). A steady-state model was used to quantify vertical export of particulate 210Po. Vertical advection was incorporated into one version of the model using time-averaged vertical velocity, which had substantial variance. This resulted in large uncertainties for the 210Po export flux in this model, suggesting that those calculations of 210Po export fluxes should be used with great care. Despite the large uncertainties, there is no question that the deficits of 210Po in the Iberian Basin and at the Greenland Shelf have been strongly affected by vertical advection. Using the export flux of 210Po and the particulate organic carbon (POC) to 210Po ratio of total (\u3e1μm) particles, we determined the POC export fluxes along the transect. Both the magnitude and efficiency of the estimated POC export flux from the surface ocean varied spatially within our study region. Export fluxes of POC ranged from negligible to 10mmolCm-2d-1, with enhanced POC export in the Labrador Sea. The cruise track was characterized by overall low POC export relative to net primary production (export efficiency \u3c1%-15%), but relatively high export efficiencies were seen in the basins where diatoms dominated the phytoplankton community. The particularly low export efficiencies in the Iberian Basin, on the other hand, were explained by the dominance of smaller phytoplankton, such as cyanobacteria or coccolithophores. POC fluxes estimated from the 210Po210Pb and 234Th238U disequilibria agreed within a factor of 3 along the transect, with higher POC estimates generally derived from 234Th. The differences were attributed to integration timescales and the history of bloom events. © 2019 Author(s)

Quantifying 210Po/210Pb disequilibrium in seawater: A comparison of two precipitation methods with differing results

The disequilibrium between lead-210 (210Pb) and polonium-210 (210Po) is increasingly used in oceanography to quantify particulate organic carbon (POC) export from the upper ocean. This proxy is based on the deficits of 210Po typically observed in the upper water column due to the preferential removal of 210Po relative to 210Pb by sinking particles. Yet, a number of studies have reported unexpected large 210Po deficits in the deep ocean indicating scavenging of 210Po despite its radioactive mean life of ∼ 200 days. Two precipitation methods, Fe(OH)3 and Co-APDC, are typically used to concentrate Pb and Po from seawater samples, and deep 210Po deficits raise the question whether this feature is biogeochemically consistent or there is a methodological issue. Here, we present a compilation of 210Pb and 210Po studies that suggests that 210Po deficits at depths \u3e 300 m are more often observed in studies where Fe(OH)3 is used to precipitate Pb and Po from seawater, than in those using Co-APDC (in 68 versus 33% of the profiles analyzed for each method, respectively). In order to test whether 210Po/210Pb disequilibrium can be partly related to a methodological artifact, we directly compared the total activities of 210Pb and 210Po in four duplicate ocean depth-profiles determined by using Fe(OH)3 and Co-APDC on unfiltered seawater samples. While both methods produced the same 210Pb activities, results from the Co-APDC method showed equilibrium between 210Pb and 210Po below 100 m, whereas the Fe(OH)3 method resulted in activities of 210Po significantly lower than 210Pb throughout the entire water column. These results show that 210Po deficits in deep waters, but also in the upper ocean, may be greater when calculated using a commonly used Fe(OH)3 protocol. This finding has potential implications for the use of the 210Po/210Pb pair as a tracer of particle export in the oceans because 210Po (and thus POC) fluxes calculated using Fe(OH)3 on unfiltered seawater samples may be overestimated. Recommendations for future research are provided based on the possible reasons for the discrepancy in 210Po activities between both analytical methods

Quantifying 210Po/210Pb Disequilibrium in Seawater: A Comparison of Two Precipitation Methods With Differing Results

The disequilibrium between lead-210 (210Pb) and polonium-210 (210Po) is increasingly used in oceanography to quantify particulate organic carbon (POC) export from the upper ocean. This proxy is based on the deficits of 210Po typically observed in the upper water column due to the preferential removal of 210Po relative to 210Pb by sinking particles. Yet, a number of studies have reported unexpected large 210Po deficits in the deep ocean indicating scavenging of 210Po despite its radioactive mean life of ∼ 200 days. Two precipitation methods, Fe(OH)3 and Co-APDC, are typically used to concentrate Pb and Po from seawater samples, and deep 210Po deficits raise the question whether this feature is biogeochemically consistent or there is a methodological issue. Here, we present a compilation of 210Pb and 210Po studies that suggests that 210Po deficits at depths &gt;300 m are more often observed in studies where Fe(OH)3 is used to precipitate Pb and Po from seawater, than in those using Co-APDC (in 68 versus 33% of the profiles analyzed for each method, respectively). In order to test whether 210Po/210Pb disequilibrium can be partly related to a methodological artifact, we directly compared the total activities of 210Pb and 210Po in four duplicate ocean depth-profiles determined by using Fe(OH)3 and Co-APDC on unfiltered seawater samples. While both methods produced the same 210Pb activities, results from the Co-APDC method showed equilibrium between 210Pb and 210Po below 100 m, whereas the Fe(OH)3 method resulted in activities of 210Po significantly lower than 210Pb throughout the entire water column. These results show that 210Po deficits in deep waters, but also in the upper ocean, may be greater when calculated using a commonly used Fe(OH)3 protocol. This finding has potential implications for the use of the 210Po/210Pb pair as a tracer of particle export in the oceans because 210Po (and thus POC) fluxes calculated using Fe(OH)3 on unfiltered seawater samples may be overestimated. Recommendations for future research are provided based on the possible reasons for the discrepancy in 210Po activities between both analytical methods

High particulate organic carbon export during the decline of a vast diatom bloom in the Atlantic sector of the Southern Ocean

Carbon fixation by phytoplankton plays a key role in the uptake of atmospheric CO2 in the Southern Ocean. Yet, it still remains unclear how efficiently the particulate organic carbon (POC) is exported and transferred from ocean surface waters to depth during phytoplankton blooms. In addition, little is known about the processes that control the flux attenuation within the upper twilight zone. Here, we present results of downward POC and particulate organic nitrogen fluxes during the decline of a vast diatom bloom in the Atlantic sector of the Southern Ocean in summer 2012. We used thorium-234 (234Th) as a particle tracer in combination with drifting sediment traps (ST). Their simultaneous use evidenced a sustained high export rate of 234Th at 100 m depth in the weeks prior to and during the sampling period. The entire study area, of approximately 8000 km2, showed similar vertical export fluxes in spite of the heterogeneity in phytoplankton standing stocks and productivity, indicating a decoupling between production and export. The POC fluxes at 100 m were high, averaging 26±15 mmol C m−2 d−1, although the strength of the biological pump was generally low. Only <20% of the daily primary production reached 100 m, presumably due to an active recycling of carbon and nutrients. Pigment analyses indicated that direct sinking of diatoms likely caused the high POC transfer efficiencies (~60%) observed between 100 and 300 m, although faecal pellets and transport of POC linked to zooplankton vertical migration might have also contributed to downward fluxes

The export flux of particulate organic carbon derived from 210Po/210Pb disequilibria along the North Atlantic GEOTRACES GA01 transect : GEOVIDE cruise

Unidad de excelencia María de Maeztu MdM-2015-0552The disequilibrium between 210Po activity and 210Pb activity in seawater samples was determined along the GEOTRACES GA01 transect in the North Atlantic during the GEOVIDE cruise (May-June 2014). A steady-state model was used to quantify vertical export of particulate 210Po. Vertical advection was incorporated into one version of the model using time-averaged vertical velocity, which had substantial variance. This resulted in large uncertainties for the 210Po export flux in this model, suggesting that those calculations of 210Po export fluxes should be used with great care. Despite the large uncertainties, there is no question that the deficits of 210Po in the Iberian Basin and at the Greenland Shelf have been strongly affected by vertical advection. Using the export flux of 210Po and the particulate organic carbon (POC) to 210Po ratio of total (>1µm) particles, we determined the POC export fluxes along the transect. Both the magnitude and efficiency of the estimated POC export flux from the surface ocean varied spatially within our study region. Export fluxes of POC ranged from negligible to 10 mmolCm−2 d−1, with enhanced POC export in the Labrador Sea. The cruise track was characterized by overall low POC export relative to net primary production (export efficiency <1%-15%), but relatively high export efficiencies were seen in the basins where diatoms dominated the phytoplankton community. The particularly low export efficiencies in the Iberian Basin, on the other hand, were explained by the dominance of smaller phytoplankton, such as cyanobacteria or coccolithophores. POC fluxes estimated from the 210Po/210Pb and 234Th/238U disequilibria agreed within a factor of 3 along the transect, with higher POC estimates generally derived from 234Th. The differences were attributed to integration timescales and the history of bloom events

Tissue engineering by decellularization and 3D bioprinting

Discarded human donor organs have been shown to provide decellularized extracellular matrix (dECM) scaffolds suitable for organ engineering. The quest for appropriate cell sources to satisfy the need of multiple cells types in order to fully repopulate human organ-derived dECM scaffolds has opened new venues for the use of human pluripotent stem cells (hPSCs) for recellularization. In addition, three-dimensional (3D) bioprinting techniques are advancing towards the fabrication of biomimetic cell-laden biomaterial constructs. Here, we review recent progress in decellularization/recellularization and 3D bioprinting technologies, aiming to fabricate autologous tissue grafts and organs with an impact in regenerative medicine

Distribution and export of particulate organic carbon in East Antarctic coastal polynyas

Polynyas represent regions of enhanced primary production because of the low, or absent, sea-ice cover coupled with the proximity of nutrient sources. However, studies throughout the Southern Ocean suggest elevated primary production does not necessarily result in increased carbon export. Three coastal polynyas in East Antarctica and an off-shelf region were visited during the austral summer from December 2016 to January 2017 to examine the vertical distribution and concentration of particulate organic carbon (POC). Carbon export was also examined using thorium-234 (234Th) as a proxy at two of the polynyas. Our results show that concentrations and integrated POC stocks were higher within the polynyas compared to the off-shelf sites. Within the polynyas, vertical POC concentrations were higher in the Mertz and Ninnis polynyas compared to the Dalton polynya. Similarly, higher carbon export was measured in the diatom-dominated Mertz polynya, where large particles ( \u3e 53 μm) represented a significant fraction of the particulate 234Th and POC (average 50 % and 39 %, respectively), compared to the small flagellate-dominated Dalton polynya, where almost all the particulate 234Th and POC were found in the smaller size fraction (1 – 53 μm). The POC to Chlorophyll-a ratios suggest that organic matter below the mixed layer in the polynyas consisted largely of fresh phytoplankton at this time of the year. In combination with a parallel study on phytoplankton production at these sites, we find that increased primary production at these polynyas does lead to greater concentrations and export of POC and a higher POC export efficiency

Biogenic sinking particle fluxes and sediment trap collection efficiency at Ocean Station Papa

© The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Estapa, M., Buesseler, K., Durkin, C. A., Omand, M., Benitez-Nelson, C. R., Roca-Marti, M., Breves, E., Kelly, R. P., & Pike, S. Biogenic sinking particle fluxes and sediment trap collection efficiency at Ocean Station Papa. Elementa: Science of the Anthropocene, 9(1), (2021): 00122, https://doi.org/10.1525/elementa.2020.00122.Comprehensive field observations characterizing the biological carbon pump (BCP) provide the foundation needed to constrain mechanistic models of downward particulate organic carbon (POC) flux in the ocean. Sediment traps were deployed three times during the EXport Processes in the Ocean from RemoTe Sensing campaign at Ocean Station Papa in August–September 2018. We propose a new method to correct sediment trap sample contamination by zooplankton “swimmers.” We consider the advantages of polyacrylamide gel collectors to constrain swimmer influence and estimate the magnitude of possible trap biases. Measured sediment trap fluxes of thorium-234 are compared to water column measurements to assess trap performance and estimate the possible magnitude of fluxes by vertically migrating zooplankton that bypassed traps. We found generally low fluxes of sinking POC (1.38 ± 0.77 mmol C m–2 d–1 at 100 m, n = 9) that included high and variable contributions by rare, large particles. Sinking particle sizes generally decreased between 100 and 335 m. Measured 234Th fluxes were smaller than water column 234Th fluxes by a factor of approximately 3. Much of this difference was consistent with trap undersampling of both small (1 mm) and with zooplankton active migrant fluxes. The fraction of net primary production exported below the euphotic zone (0.1% light level; Ez-ratio = 0.10 ± 0.06; ratio uncertainties are propagated from measurements with n = 7–9) was consistent with prior, late summer studies at Station P, as was the fraction of material exported to 100 m below the base of the euphotic zone (T100, 0.55 ± 0.35). While both the Ez-ratio and T100 parameters varied weekly, their product, which we interpret as overall BCP efficiency, was remarkably stable (0.055 ± 0.010), suggesting a tight coupling between production and recycling at Station P.The authors would like to acknowledge funding support from the NASA EXPORTS program (Award 80NSSC17K0662) for all sediment trap data presented here. Net primary production data collection was supported by EXPORTS (Award 80NSSC17K568) to Oregon State University. Thorium data collection was supported by EXPORTS (Award 80NSSC17K0555) to KB, CRBN, and L. Resplandy