Abstract
Of the ~240 × 1012 mol year−1 of biogenic silica (bSi) produced by diatoms and other silicifying organisms, only roughly 3%–4% escapes dissolution to be permanently buried. At the global scale, how, where and why bSi is preserved in sediment is not well understood. To help address this, I compile 6245 porewater dissolved Si concentrations from 453 sediment cores, to derive the concentration gradient at the sediment–water interface and thus diffusive fluxes out of the sediment. These range from <0.002 to 3.4 mol m−2 year−1, and are independent of temperature, depth and latitude. When classified by sediment lithology, predominantly siliceous sediments unsurprisingly have higher mean diffusive fluxes than predominantly calcareous or clay-rich sediment. Combined with the areal extent of these lithologies, the ‘best-guess’ global sedimentary bSi recycling flux is 69 × 1012 mol year−1.
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1 Introduction
Ocean dissolved Si concentrations (hereafter [Si]) span two orders of magnitude, from <1 μmol L−1 in surface gyres to almost 200 μmol L−1 in parts of the deep ocean. Yet even these regions are highly undersaturated—amorphous Si solubility is ca. 1800 μmol L−1 at 20 °C (Gunnarsson and Arnórsson 2000). The ubiquitously high degree of undersaturation attests to the efficiency with which biosilicifying organisms, in particular the diatoms, can take dissolved Si and precipitate it in their biogenic silica (bSi) skeletons. This high degree of undersaturation also means that much of the bSi produced dissolves after the organism’s death. Dissolution begins in the euphotic zone, and continues throughout the water column and into the upper sediment, until the bSi is exhausted (leading to large parts of the ocean floor devoid of siliceous remains) or the bSi reaches equilibrium with sediment porewaters and dissolution ceases.
The canonical figure for annual bSi production is 240 Tmol (Tréguer and De La Rocha 2013), approximately 25× annual inputs of Si to the ocean (Frings et al. 2016). Various approaches consistently indicate a large fraction—around 50%–60%—is remineralised in the upper 100 m. This leaves around 100 Tmol year−1 bSi as export production (Tréguer and De La Rocha 2013). The fate of this bSi is less well understood, though ca. 10 Tmol year−1 must be preserved to balance the inputs at steady-state. In particular, the relative fractions of dissolution occurring in the water column and in the sediments are not well constrained, but has implications for how we quantify the past and present Si cycle. Diffusive fluxes of Si across the sediment–water interface can be used to estimate bSi dissolution in the sediment; previous global scale estimates include 8–38 Tmol year−1 (Treguer et al. 1995), 25.5 Tmol year−1 (Laruelle et al. 2009) and 33–159 Tmol year−1 (Tréguer and De La Rocha 2013). Clearly, there is scope to improve these estimates. Here, I attempt this by using a compilation of porewater [Si] profiles from marine sediments to calculate diffusive Si fluxes out of sediment.
2 Methods
I compiled >450 published porewater [Si] records from the upper 40 cm of marine sediment cores (Fig. 1), assuming that the different methods of coring and sample collection yield comparable results. Most studies kept cores at in-situ temperatures to avoid chemical changes, though no attempt was made to identify and account for those that did not. Both theoretical and empirical studies have shown that porewater [Si] profiles can be described as an exponential function (e.g. McManus et al. 1995; Fig. 1):
where \(C_{asym}\) is an asymptotic concentration, \(C_{0}\) is the overlying water concentration, \(\beta\) an exponential constant (cm−1) and z the depth below sediment surface (cm). Values of \(C_{asym}\) and \(\beta\) were obtained for each profile by searching for the combination that minimised the RMSE between predicted and measured values. The 5% of poorest model fits were discarded. Differentiation of Eq. (1) at z = 0 provides the gradient across the sediment–water interface:
which can then be used in Fick’s first law to calculate the flux J (mol m−2 year−1) across the sediment–water interface, assuming steady-state porewater DSi:
where D is dissolved Si diffusion coefficient which takes a value of ca. 0.03 m2 year−1 at 25 °C (Wollast and Garrels 1971), and is corrected for sediment tortuosity and temperature after Boudreau (1996). In-situ temperature was extracted from the closest grid-cell of the WOCE ocean climatology (Gouretski and Koltermann 2004). A representative, uniform value of surface sediment porosity Φ (also required for the tortuosity correction) was prescribed at 0.9 for all sites. Finally, sediment lithology was identified at each location using the 0.1° resolution classification of Dutkiewicz et al. (2015).
3 Results and discussion
In total, 453 porewater profiles were compiled, of which 325 were at sufficiently high resolution to be included in the analysis. These data span the global ocean (Fig. 1B), though are biased towards the Atlantic. Calculated asymptote concentrations (\(C_{asym}\)) range from 9 to 862 μmol L−1, and \(\beta\) values from 0.01 to 6 cm−1. In all cases, the flux across the sediment–water interface was positive and ranges from 0.0017 to 3.35 mol m−2 year−1, with mean = 0.22 and median = 0.10 mol m−2 year−1. The fluxes are lognormally distributed, and are not systematically related to temperature, core depth or latitude (Fig. 2). Asymptote concentrations and exponential constants (\(\beta\)) are similarly unrelated to these parameters (data not shown).
Although the data is noisy, there are significant differences in diffusive fluxes from different sediment lithologies (Fig. 2A). Taking the area of these lithologies from the Dutkiewicz et al. (2015) digital map together with their diffusive fluxes (fitted to a lognormal distribution and using a Monte Carlo approach to uncertainty propagation) yields a median total flux of 69.5 Tmol year−1 (5th–95th percentiles: 64–232 Tmol year−1), of which only 16.5 Tmol year−1 is from areas classified as siliceous (i.e. diatom, radiolarian or sponge oozes, or siliceous/siliceous-calcareous mud. The remainder (median = 44.9 Tmol year−1) comes from clay or calcareous sediments, which together cover 284 × 106 km2, or about 78% of ocean area (Dutkiewicz et al. 2015). This suggests regions not typically considered important in the ocean Si cycle may deserve more attention, simply because of their spatial extent. Tréguer and De La Rocha (2013) had previously considered diffusion from non-siliceous sediments to reflect dissolution/alteration of ocean basalts or terrigenous sediments. They employed an areal diffusive flux rate of 10–20 mmol m−2 year−1 from the study of Sayles et al. (1996), which is an order of magnitude less than the rate derived here for non-siliceous sediments. Either the dissolution of ocean basalt and terrigenous detrital sediment is greatly underestimated in recent budgets, or there is a more active benthic biological Si cycle in these regions than conventionally recognised, perhaps via sponges (e.g. Alvarez et al. in review). A discrepancy also exists between the amount of bSi thought to arrive at the seafloor and that calculated to dissolve within the sediments. According to the sediment trap analysis of Honjo et al. (2008), 34.6 Tmol year−1 bSi sinks past 2 km. About 86% of ocean floor is below this depth, and given the lack of correlation between water depth and Si diffusive fluxes (Fig. 2C), then ca. 60 Tmol year−1 is calculated here to dissolve below this depth. This remains to be explained.
Assuming the marine Si cycle is close to steady-state, then ca. 9.5 × 1012 mol bSi year−1 is permanently buried (Frings et al. 2016), broadly consistent with independent estimates of bSi burial (e.g. DeMaster 2002). This implies a globally averaged sediment preservation efficiency of ca. 12%, in the same range as derived for individual regions (see e.g. Ragueneau et al. 2009). This analysis confirms that a large fraction of bSi dissolution takes place in the sediment rather than the water column. The best estimate for the total dissolution flux is 69.5 Tmol year−1, though the large associated uncertainties suggest it is rather more poorly understood than previously realised.
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11th International Symposium on Geochemistry of the Earth’s Surface.
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Frings, P. Revisiting the dissolution of biogenic Si in marine sediments: a key term in the ocean Si budget. Acta Geochim 36, 429–432 (2017). https://doi.org/10.1007/s11631-017-0183-1
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DOI: https://doi.org/10.1007/s11631-017-0183-1