Salinity control on Na incorporation into calcite tests of the planktonic foraminifera Trilobatus sacculifer – evidence from culture experiments and surface sediments
- 1GEOMAR Helmholtz Centre for Ocean Research Kiel, Wischhofstr. 1–3, 24148 Kiel, Germany
- 2Department of Ocean System Sciences, Royal Netherlands Institute for Sea Research, and Utrecht University, Texel, the Netherlands
- 3Department of Oceanography, Dalhousie University, 1355 Oxford Street, P.O. Box 15000, Halifax, Nova Scotia, B3H 4R2, Canada
- 4Department of Earth Sciences, Faculty of Geosciences, Utrecht University, Heidelberglaan 2, 3584 CS Utrecht, the Netherlands
- 5Marine Biogeosciences, Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany
Correspondence: Jacqueline Bertlich (firstname.lastname@example.org)
The quantitative reconstruction of past seawater salinity has yet to be achieved, and the search for a direct and independent salinity proxy is ongoing. Recent culture and field studies show a significant positive correlation of Na∕Ca with salinity in benthic and planktonic foraminiferal calcite. For accurate paleoceanographic reconstructions, consistent and reliable calibrations are necessary, which are still missing. In order to assess the reliability of foraminiferal Na∕Ca as a direct proxy for seawater salinity, this study presents electron microprobe Na∕Ca data measured on cultured specimens of Trilobatus sacculifer. The culture experiments were conducted over a wide salinity range of 26 to 45, while temperature was kept constant. To further understand potential controlling factors of Na incorporation, measurements were also performed on foraminifera cultured at various temperatures in the range of 19.5 to 29.5 ∘C under constant salinity conditions. Foraminiferal Na∕Ca values positively correlate with seawater salinity (, R=0.97, p<0.005). Temperature, on the other hand, exhibits no statistically significant relationship with Na∕Ca values, indicating salinity to be one of the dominant factors controlling Na incorporation. The culturing results are corroborated by measurements on T. sacculifer from Caribbean and Gulf of Guinea surface sediments, indicating no dissolution effect on Na∕Ca in foraminiferal calcite with increasing water depth up to >4 km. In conclusion, planktonic foraminiferal Na∕Ca can be applied as a potential proxy for reconstructing sea surface salinities, although species-specific calibrations might be necessary.
The combination of foraminiferal Mg∕Ca and stable oxygen isotopes (δ18O) measured on the same specimens is a well-established approach to estimate both past sea surface temperatures (SSTs) and δ18O of seawater (δ18Osw) (Elderfield and Ganssen, 2000; Anand et al., 2003; Flower et al., 2004). When corrected for past changes in global ice volume and individual temperature effects, the ice volume free δ18Oivf−sw indicates past changes in salinity (S) caused by changes in evaporation, precipitation, and freshwater fluxes such as river discharge (Rohling and Bigg, 1998; Rosenthal et al., 2000; Weldeab et al., 2007). Quantitative assessments of past sea surface salinity (SSS) may be erroneous, however, as the relationship between δ18Osw and salinity varies in space and most likely also time due to variable freshwater contributions, for instance, from river discharge or meltwater flux (Rohling and Bigg, 1998).
Weldeab et al. (2007) applied Ba∕Ca in planktonic foraminifera as an independent tool for quantitative reconstructions of salinity near rivers. Ba∕Ca of river water is an order of magnitude higher than that of seawater (Weldeab et al., 2007; Schmidt and Lynch-Stieglitz, 2011; Hönisch et al., 2011). Therefore, high foraminiferal Ba∕Ca values provide evidence of increased continental runoff due to precipitation changes in the hinterland (Hall and Chan, 2004; Hoffmann et al., 2014; Bahr et al., 2018). Ba∕Caforam is apparently not influenced by temperature changes within 7 ∘C and hence linearly correlated with Ba changes in seawater, but its applicability as a salinity proxy is still limited to regions close to river mouths (Weldeab et al., 2007; Bahr et al., 2013). Another theoretical and indirect approach to reconstruct salinity changes is based on the correlation of stable oxygen isotopes (δ18O) and stable hydrogen isotope ratios (δD) between surface waters and the hydrological cycle (Schouten et al., 2006; Rohling, 2007). However, these different ratios must be measured on different archives such as foraminifera calcite (δ18O) and alkenones (δD), whereby salinity reconstructions are inherently limited by an uncertainty of at least one salinity unit (Rohling, 2007).
Because of the limitations in current approaches for the quantitative reconstruction of past salinities, the search for a direct salinity proxy is ongoing. Recent culture experiments demonstrated a significant positive correlation between seawater salinity and Na∕Ca in foraminiferal calcite of the intertidal benthic foraminifer Ammonia tepida (Wit et al., 2013) and the planktonic species Globigerinoides ruber (pink) (Allen et al., 2016). A field calibration study of living specimens (G. ruber (white) and Trilobatus sacculifer) from the Red Sea confirms the positive correlation between Na∕Caforam and salinity, although measured Na∕Ca values were much higher (Mezger et al., 2016) compared to our culture studies.
Further studies are therefore essential to assess previous results and to understand the main controlling factors on foraminiferal Na incorporation. It is important to know how certain species react to extreme environmental changes and what their tolerance limits are to confirm the robustness of Na∕Ca as a salinity proxy over a broad salinity range. Here, we present electron microprobe measurements on Trilobatus sacculifer, which were cultured over a salinity range between 26 and 45 (Bijma et al., 1990b; Nürnberg et al., 1996). Salinity ranges used in previous culture studies were rather limited, with salinities of >30 and <40 (Wit et al., 2013: S30–39; Allen et al., 2016: S33–40). The high spatial resolution of the microprobe technique used here provides further insights into the inter- and intra-specimen variability of Na∕Ca and potential mechanisms involved in Na incorporation. Temperature experiments with cultured T. sacculifer grown at temperatures from 19.5 to 29.5 ∘C and constant salinity (Bijma et al., 1990b; Nürnberg et al., 1996) were performed to check for a potential temperature effect on Na incorporation, as previously suggested by Allen et al. (2016) and Mezger et al. (2016).
In addition, early diagenetic processes can significantly alter the geochemical signal of fossil foraminifera, while the empty tests settle through the water column and are buried in deep-sea sediments (Elderfield and Ganssen, 2000; Regenberg et al., 2006). Previous studies have shown that foraminiferal Mg∕Ca, Cd∕Ca, and Ba∕Ca are affected by calcite dissolution (McCorkle et al., 1995; Brown and Elderfield, 1996; Dekens et al., 2002; Regenberg et al., 2006, 2014). To assess potential geochemical alteration we compare Na∕Caforam results of T. sacculifer from culture experiments and from Caribbean and Gulf of Guinea surface sediments.
2.1 Foraminiferal species studied
The planktonic foraminifer T. sacculifer is a spinose, symbiont-bearing species and its chemical composition (e.g., Mg∕Ca, Nürnberg et al., 1996; δ18O, Elderfield and Ganssen, 2000) is widely used in paleoceanography to reconstruct environmental conditions at the ocean's surface. Here, we use the new genus name Trilobatus instead of Globigerinoides following Spezzaferri et al. (2015), since the latter genus is polyphyletic in its traditional perception based on the presence of supplementary apertures on the spiral side. The species T. sacculifer and T. trilobus are the same biological species and genetically identical (Hemleben et al., 1987; Bijma and Hemleben, 1994; André et al., 2013; Spezzaferri et al., 2015). They depict different morphotypes that developed during certain ontogenetic stages and were therefore not separated in the present study.
In the Caribbean, T. sacculifer preferentially inhabits water depths between 10 and 30 m (Jones, 1968; Hemleben et al., 1987). The average habitat depth of this species is between 31 and 50 m in the eastern Caribbean (Jentzen et al., 2018), with the highest abundances from 0–20 m (Schmuker and Schiebel, 2002). In the eastern tropical Atlantic, T. sacculifer calcifies ontogenetically in the mixed layer at 0–30 m, and slightly deeper in the western tropical Atlantic (0–80 m) within the photic zone above the pycnocline (Ravelo and Fairbanks, 1992; Steph et al., 2009; Jentzen et al., 2018). In the subtropical eastern North Atlantic, T. sacculifer is most abundant between ∼30 and 60 m (Rebotim et al., 2017). Prior to gametogenesis at the end of its life cycle, a process related to reproduction, T. sacculifer descends through the water column and precipitates gametogenic calcite after discarding spines (Bé, 1980; Bijma et al., 1990a; Bijma and Hemleben, 1994). The formation of a final sac-like chamber is a sign that gametogenesis is impending within 24 h (Bé, 1980; Hemleben et al., 1989; Erez, 2003).
Since T. sacculifer preferentially calcifies in the mixed layer at high light intensities, an averaged habitat depth of 30 m is assumed for this study. Further, T. sacculifer is present throughout the year and shell fluxes do not vary significantly with seasonal changes in the tropic and subtropical water masses when the annual SST is ≥25 ∘C (Bijma et al., 1990a, b; Bijma and Hemleben, 1994; Schmuker and Schiebel, 2002; Lin et al., 2004; Jonkers and Kučera, 2015). Accordingly, annual salinity and temperature values of 30 m water depth were taken from the World Ocean Atlas (WOA) 2013 (Zweng et al., 2013; Locarnini et al., 2013; Schlitzer, 2015) and correlated with the geochemical results of this study.
a Foraminifera were handpicked from the 300–400 µm size fraction. Each Na∕Ca value derives from the average of 30 specimens and is the mean of three to five repeated ICP-OES measurements. b Foraminifera were selected from the 315–400 µm size fraction. Every ICP-OES measurement was repeated five times. One sample contains 20–30 specimens.
2.2 Culture experiments
Two sets of culture experiments are described. For both, specimens of the planktonic foraminiferal species T. sacculifer (originally named as G. sacculifer in Bijma et al., 1990b and Nürnberg et al., 1996) were collected by scuba divers at 3–8 m of water depth 1–2 miles off the southern coast of Curaçao (Bijma et al., 1990b) and off the western coast of Barbados (Hemleben et al., 1987). The test length of collected foraminifera thus sampled did not exceed ∼110–500 µm, but only specimens with a similar test size were chosen for each experiment (Bijma et al., 1990b). For salinity experiments, specimens were grown in filtered seawater from the sampling site at salinities of 26, 41, 44, and 45 (abbreviated as S26–45 below). The different salinities were achieved by evaporating natural seawater at 50 ∘C or diluting with distilled water. The temperature was held constant at 26.5 ∘C during salinity experiments. Detailed information on culture protocols and experiments is given in Bijma et al. (1990b) and Nürnberg et al. (1996).
For the temperature experiment, specimens were grown in unfiltered seawater from the sampling site at temperatures of 19.5, 23.5, 26.5, and 29.5 ∘C (all ±0.25 ∘C), while keeping salinity changes to a minimum (Hemleben et al., 1987). The experiments were run during different seasons between 1980 and 1984, and because salinity varied in the winter and summer season between ∼36 and ∼31 at the sampling sites caused by Orinoco and Amazon freshwater discharges, the temperature experiments were divided into 33 salinity (S33) and 36 salinity (S36) groups (see Hemleben et al., 1987, for more details). The salinity increased by 0.5–0.8 during the 29.5 ∘C experiment by evaporation in the water bath (Nürnberg et al., 1996). Electron microprobe measurements were carried out on newly grown chambers at defined salinity and temperature conditions. The final newly grown chamber, the penultimate chamber, and prior chambers are labeled as F (for final), F-1, F-2, F-3, and so forth.
2.3 Surface sediment samples
Foraminiferal tests collected from Caribbean surface sediment samples were used to gain information about the natural interspecific variation of Na∕Ca in an open ocean setting with only minor annual changes in salinity and temperature (Fig. 1, Table 1). Undisturbed surface sediments were retrieved using a multicorer (MUC) during RV Sonne cruise SO164 (Nürnberg et al., 2003). Sample locations and their respective bottom water depths are shown in Fig. 1a and Table 1. Planktonic foraminifera were selected from the uppermost sediment layer (0–1 cm) and handpicked from the 315–400 µm size fraction. This narrow size fraction was chosen to avoid possible size effects, as known for Mg∕Ca values (e.g., Elderfield et al., 2002), or a bias of ontogenetic variations (e.g., Lin et al., 1997). Further, only foraminifera with intact, unbroken, and visually (using a binocular microscope) unaltered tests were selected for analysis. This procedure also holds for the Gulf of Guinea surface sediment samples.
The ages of Caribbean surface sediments are late Holocene; specifically, they are most likely younger than 2000–3000 years (AMS14C ages before present, BP) (Regenberg et al., 2009; Table 1). During this time period, Caribbean sea surface temperature (SST) varied by ±1–2 ∘C at most (Keigwin, 1996; Watanabe et al., 2001; Haase-Schramm et al., 2003).
Surface waters at the sampling locations are composed of Caribbean Surface Water (CSW), characterized by lower salinities throughout the year (S∼33.7–36.3) than the underlying subtropical underwater mass at depths of 100–300 m, reaching a salinity maximum of ∼37.2 (Corredor and Morell, 2001; Schmuker and Schiebel, 2002; Haase-Schramm et al., 2003; Schönfeld et al., 2011). The CSW is mainly fed by trade-wind-driven water masses of the tropical and subtropical Atlantic, entering the NE Caribbean through the Lesser Antilles (Gordon, 1967). Moreover, the CSW is seasonally influenced by local precipitation and freshwater input from the Orinoco and Amazon rivers in response to shifts of the Intertropical Convergence Zone (Busalacchi and Picaut, 1983; Gordon, 1967). In spite of seasonal variations, the annual sea surface salinity across the Caribbean is restricted to variations between 35.1 and 36.3 (±0.4) at 30 m of depth (Schlitzer, 2015; Zweng et al., 2013, Fig. 1c). Annual SST varies between 26.8 and 27.7 ∘C (Locarnini et al., 2013; Fig. 1d).
2.3.2 Gulf of Guinea
In addition to the Caribbean samples, surface sediments were chosen from six core locations (GIK16860 to GIK16808) in the Gulf of Guinea, located in the eastern equatorial Atlantic (Fig. 1b–d, Table 1). The surface sediments were retrieved by giant box corers from January to February 1988 during RV Meteor cruise M6–5 (Lutze et al., 1988; Altenbach et al., 2003). Foraminiferal samples were taken from the uppermost sediment layer (0–1 cm). For geochemical analyses, specimens of T. sacculifer were handpicked from the 300–400 µm size fraction. Radiocarbon ages are not available for these surface sediments, but the study of Regenberg et al. (2009) estimates ages of 2430–2730±40–50 years BP for eastern Atlantic surface sediments proximal to the Gulf of Guinea.
The Gulf of Guinea is influenced by high rates of monsoon-controlled precipitation and large freshwater discharges from the adjacent Sanaga and Niger rivers, with the highest input during June to September (Altenbach et al., 2003; Weldeab et al., 2007). The annual SSS varies from east to west at surface waters from ∼32 to 35 and increases within the same range from ∼32 to 36 with water depth (0–60 m), but is strongly dependent on proximity to river mouths (Schlitzer, 2015; Zweng et al., 2013; Fig. 1b, c). The annual SST varies around 27.6 ∘C (±0.6 ∘C) and decreases with depth to ∼19 ∘C at 60 m (Schlitzer, 2015; Locarnini et al., 2013; Fig. 1d).
2.3.3 Dissolution effect on foraminiferal Na∕Ca
To examine the possible effect of calcite dissolution on partial Na+ removal from foraminiferal calcite with increasing water depth, we provide the calcite saturation state of bottom waters at all sampling sites from Caribbean and Gulf of Guinea surface sediments (Fig. 6b). The is defined as the difference between the in situ carbonate ion concentration () and at calcite saturation and has been shown to be crucial for the selective ion removal of Mg2+ from foraminiferal calcite (Brown and Elderfield, 1996; Regenberg et al., 2006). The present day calcite saturation horizon at which is 0 µmol kg−1, is at ∼4.7 km in the Caribbean and ∼4.4 km in the Gulf of Guinea (Regenberg et al., 2006, 2014; Fig. 6b). According to Regenberg et al. (2014), the onset of planktonic foraminiferal Mg∕Ca dissolution occurs globally below a critical calcite saturation level in bottom waters of µmol kg−1. This critical threshold is reached at water depths around ∼3.5 km in the Caribbean and ∼2 km in the Gulf of Guinea. Below, Mg∕Ca values decline linearly by mmol mol−1 per µmol kg−1 (Regenberg et al., 2006, 2014). Conversely, Mg∕Caforam values are stable at supersaturated bottom waters with µmol kg−1 or above 400 m water depths (Regenberg et al., 2006, 2014). Although a clear dependence of foraminiferal Mg∕Ca with water depth and is shown in previous studies, no data are available yet about the Na∕Ca to relationship over time and with water depth in foraminiferal calcite. Hence, we assume a similar threshold (∼21 µmol kg−1) for our Na∕Ca results at which the onset of partial Na+ removal could possibly start, which needs further study.
Bottom water values for Caribbean surface sediments presented here are taken from preexisting datasets for the same core locations from Regenberg et al. (2006). To calculate , Regenberg et al. (2006) used total alkalinity (TA) and TCO2 data from the World Ocean Circulation Experiment (WOCE) (RV Knorr cruise 1997, section A22, campaign 316N151_4; https://cchdo.ucsd.edu/, last access: 26 June 2018). Calculated bottom water values for the Gulf of Guinea water depth profile were adopted from Weldeab et al. (2016) and Weldeab (2012) for overlapping core locations. Missing values were calculated with the program CO2SYS by Pierrot et al. (2006) using the constants K1 and K2 following Mehrbach et al. (1973), refitted by Dickson and Millero (1987), and the constant by Dickson (1990). To calculate the in situ carbonate concentration, the respective data (TA, TCO2, pCO2, pH, salinity, temperature, pressure, total phosphate, and silicate) were taken from WOCE (RV L'Atlante cruise, section A13, campaign 35A3CITHER3_2; https://cchdo.ucsd.edu/). The at saturation was calculated after Jansen et al. (2002).
2.4 Sample preparation and electron microprobe analysis of cultured foraminifera
Three individual foraminifera per salinity experiment and five individual foraminifera for every temperature experiment were selected from the same size fraction (250–400 µm). Only specimens without a sac-like final chamber were chosen for geochemical analysis to avoid a potential impact from factors other than those targeted here. Newly grown chambers under defined laboratory conditions were compared to chambers grown in situ before placing them in culture (Hemleben et al., 1987). For the electron microprobe analyses, all cultured specimens were mounted in epoxy resin (Nürnberg et al., 1996). To expose a fresh and planar surface of test cross sections, the sample mounts were polished with diamond-polishing pastes with a 1 µm grain size in the last step. The samples were coated with a carbon coating of 20 nm to reduce charging effects and hence to increase the spatial resolution of the obtained microprobe element maps.
The measurements were performed on a JEOL JXA 8200 electron microprobe at GEOMAR. In order to map and quantify Na distribution patterns in both single chambers and chamber wall profiles of T. sacculifer, quantitative wavelength-dispersive spectrometry (WDS) was applied. Na∕Ca values were derived from elemental maps, reaching a higher spatial resolution than point measurements (Fig. 2). Na∕Ca values of newly grown calcite were derived from at least six single maps along the inner (non-gametogenic) part of the relevant chamber, varying in size between 5 µm × 5 µm and 10 µm × 20 µm (Fig. 2). Calcium intensities (wt %) deviating more than 10 % from the maximum Ca intensity within one map were discarded to ensure that measurements affected by pores or cracks within the test were excluded. Further, to avoid a mixed signal, maps with accumulated higher Na concentrations (±2σ) at calcite spines and spine bases were not integrated into the calibration (referring to Branson et al., 2016). Every pixel within a map is 1 µm in diameter and has an element intensity. Pixels were averaged for the entire map (Fig. 2). The maps were generated with a focused electron beam, adjusted with an acceleration voltage of 15 kV, a beam current of 80 nA, and a spot diameter and step size of 1 µm. The dwell time was set at 50 ms per measurement with five accumulations, resulting in a total measurement time of 250 ms on the peak position. Na and Ca intensities were measured with the crystals TAPH (Kα) and PETH (Kα). The background intensities were measured separately at almost the same sample location with exactly the same settings and 250 ms of accumulation time.
Absolute Na∕Ca values were calculated using a constant calibration factor for each element after subtracting the background intensities from the total element intensities. The obtained net intensities were converted to concentrations and corrected to known concentrations (in wt %) from referenced materials (Table 2). Measurements on standard materials were performed with 10 µm × 10 µm maps (number of pixels: n=100). The precision of the element analysis and the uncertainty between single measurements are given by the relative standard deviation of averaged element maps (RSD = (standard deviation (1σ)∕mean value) ⋅ 100) in percent, which is less than 5 % for the standard materials used (Table 2). To check for matrix effects, the in-house standard A2 (Ohde et al., 2003), a natural modern coral with a similar elemental composition to foraminiferal calcite, was also measured. The accuracy of analyses is expressed as the relative error in percent, representing the deviation between the measured and the reference values (Table 2).
The intra-test variability is expressed as RSD in percent and is calculated from averaged Na∕Ca maps within chamber wall cross sections of one foraminifer. The inter-test variability (RSD in percent) is derived from mean Na∕Ca values of one foraminifer and exhibits differences between specimens within the same experiment. The Pearson's correlation coefficient R describes within the range of −1 to 1 the correlation between trace elements and the experimental settings, here salinity and temperature. A positive or negative correlation occurs if R is >0 or R<0. The appending p value indicates its significance. If p is less than 0.05 (5 %) the results are statistically significant. The Na∕Ca results for every culture experiment were tested for normality with the Shapiro–Wilk test and corresponding p values (Appendix A). If p is less than or equal to 0.05 (95 % confidence interval), the data are not normally distributed. The range and distribution of averaged Na∕Ca maps for each salinity and temperature experiment are shown as box and whisker plots, indicating the first and third quartiles (Fig. 3). The horizontal lines inside the box represent the mean and median. Minimum and maximum values are shown by vertical lines (whiskers) outside the box. All Na∕Ca values of culture experiments are presented with the standard error of the mean (SEM = (standard deviation )).
2.5 ICP-OES sample preparation and analysis of surface sediment samples
Traditional measurements of the elemental composition of foraminiferal calcite employ chemical cleaning procedures as pioneered by Boyle (1981). These were modified for Na∕Ca after Barker et al. (2003) as follows. Each sample consisting of 25–35 specimens from the same size fraction (Caribbean: 315–400 µm; Gulf of Guinea: 300–400 µm) was cracked under a binocular and placed in acid-cleaned PP micro-centrifuge tubes before being rinsed under ultrasonic agitation with ultrapure water (<18 MΩ) three times, ethanol, and again ultrapure water to remove clays. To eliminate metal oxides in the reductive cleaning step, 100 µL of a buffered solution of hydrous hydrazine (1 M hydrazine mixed with 0.25 M citric acid in 16 M ammonia, following the protocol of Boyle and Keigwin, 1985) was added to each vial and reacted in a hot (90 ∘C) water bath for 30 min. The samples were thoroughly rinsed to remove these chemicals with ultrapure water before being transferred to fresh acid-cleaned tubes. Residual organic matter was subsequently removed by a 0.3 % H2O2 solution (250 µL added to each vial), kept again for 20 min in a hot water bath and rinsed three times with ultrapure water. A final leaching step quickly rinsed the samples with 0.001 M HNO3 before they were finally rinsed once more with ultrapure water. The remaining water was removed and samples were diluted right before the measurements in 500 µL 0.075 M HNO3.
The elemental analyses were performed simultaneously with a Varian 720 inductively coupled plasma–optical emission spectroscope (ICP-OES) at GEOMAR. The device is equipped with a cooled cyclonic spray chamber combined with a microconcentric nebulizer (200 µL min−1 sample uptake) optimized for signal stability. The most intense element lines without interferences were chosen for elemental analysis. These wavelengths were 70.60 nm for Ca, 279.55 nm for Mg, and 589.59 nm for Na. The measurement routine repeats five times for every sample and standard solution, and the RSD of respective measurements gives an estimation of the internal error, which is 0.31 % RSD for Na and 0.22 % RSD for Ca. To correct for analytical drift of the instrument, the reference material ECRM 752-1, commonly used for foraminiferal Mg∕Ca analysis (reference value: 3.762 mmol mol−1 in Greaves et al., 2008), was measured after a set of 10 foraminifera samples (RSD: 0.06 %). As there are no Na values in the literature for the ECRM 752-1, we additionally measured the coral reference material JCp-1, with reference values of 0.586 (±0.003 SD) wt % Na2O and 53.52 (±0.29 SD) wt % CaO in Okai et al. (2002). The JCp-1 was measured after a set of 10 foraminifera samples, resulting in a average Na∕Ca value of 18.75 mmol mol mmol mol−1 (three measurements) during our ICP-OES analysis with a precision of 0.3 % (RSD). The accuracy of analysis is 5.5 %, which corresponds to a variation of ±0.54 mmol mol−1 from the reference JCp-1 Na∕Ca value.
3.1 Sodium incorporation into foraminiferal calcite
3.1.1 Salinity experiments
Averaged Na∕Ca values for the salinity experiments are presented in Table 3. Datasets for T=26.5 ∘C of both temperature experiments (S36, S33) were included into the Na∕Ca–salinity calibration. Newly grown chambers of T. sacculifer have, on average, Na∕Ca values between 3.86 and 6.40 mmol mol−1 over a range of 19 salinity units. Foraminiferal Na∕Ca values correlate positively with sea surface salinity: (R=0.97, p<0.005) and increase by 2.25 % per salinity unit, corresponding to an absolute Na∕Ca value of 0.12 mmol mol−1 (Fig. 4). Between salinities of 26 and 36, there is a marked increase in Na∕Caforam by 1–1.25 mmol mol−1 based on the lowest and highest Na∕Ca value of each experiment. The smallest possible range is detected between salinities of 33 and 36 at which Na∕Ca values increase by ∼0.5 mmol mol−1, which is 0.1 mmol mol−1 larger than the 95 % confidence interval.
Single values and the calculated intra- and inter-test variability for each experiment are presented in tabular form in Appendix B. The inter-test Na∕Ca variability (RSD in percent) ranges from 5.5 % to 6.5 % (±0.29–0.34 mmol mol−1) between single foraminifera from the same salinity experiment, which is larger than the analytical error of the electron microprobe (RSD≤0.2 %–1.2 %; Table 2). The intra-test Na∕Ca variability (between different maps on one chamber) is twice as large as the inter-test variability and varies between 7.4 % and 13.3 % (±0.39–0.70 mmol mol−1; Appendix B).
The largest ranges of Na∕Ca within one experiment are observed among foraminifera cultured at salinities >41 (Fig. 3a). Intra-test map analyses deviate within chamber cross sections of one foraminifer by ±1.1 mmol mol−1, while inter-test Na∕Ca values between foraminifera deviate by ±0.25 mmol mol−1 (S=41). For the remaining experiments at salinities<41, Na∕Ca values deviate within the same test by ±0.35–0.65 mmol mol−1 and vary among foraminifera by ±0.22–0.55 mmol mol−1, which equals the range of the 95 % confidence interval. The culture experiment conducted at a salinity of 44 deviates from previous results: Na∕Ca shows a decrease of ∼0.5 mmol mol−1 compared to the experiments at salinities below 41 (Figs. 3a, 4). According to Nürnberg et al. (1996), all specimens of the S44 experiment underwent gametogenesis and were enriched in Mg∕Ca. Because of differences in elemental composition and calcite structure between gametogenic calcite and ontogenetic calcite (Erez, 2003), the results of the S44 experiment were hence excluded from the regression shown in Fig. 4. Still, even when including foraminifera with gametogenic calcite in our calculations, Na∕Ca increases by 2 % per salinity unit (, R=0.90, p<0.01). Na∕Ca values measured on chambers (F-3, F-4) grown in situ before sampling and culturing reflect the salinity of ambient seawater in the Caribbean (S∼35.9) and correspond to the results of culture experiments at a salinity of 36 (Zweng et al., 2013; Fig. 4). Nonetheless, Na∕Ca values of chambers grown in situ were not included in the calibration because the calcification conditions are not exactly known.
3.1.2 Temperature experiments
Within the 36 salinity group, averaged Na∕Ca values of newly grown foraminiferal calcite, precipitated at temperatures from 19.5 to 29.5 ∘C, range from 3.96 to 5.49 mmol mol−1 (Table 4, Fig. 5). In the 33 salinity group, averaged Na∕Ca values vary between 4.10 and 5.78 mmol mol−1 (Table 5, Fig. 5). No significant (p<0.69 (S36), p<0.14 (S33)) correlation is found between Na∕Ca and temperature for either experiment (Fig. 5).
The inter- and intra-test variability of Na∕Ca for the different treatments is shown in Appendix B. Box and whisker plots demonstrate the Na∕Ca distribution for each temperature experiment (Fig. 3b). The inter-test variability of Na∕Ca (between single foraminifera of the same experiment), expressed as RSD, varies from 7.3 %–9.8 % (S36) and 3.2 %–11.5 % (S33), corresponding to absolute values of ±0.38–0.51 mmol mol−1 (S36) and ±0.17–0.6 mmol mol−1 (S33). Na∕Ca values vary within newly formed chambers of one test (intra-test) between 1.8 %–16.2 % (S36; ±0.09–0.85 mmol mol−1) and 3.6 %–10.6 % (S33; ±0.19–0.55 mmol mol−1). Notably, the highest Na∕Ca intra-test distribution (up to 16 %) only occurs in experiments below 24 ∘C (S36), which is in contrast to the smallest intra-test variation of 1.8 % observed for treatments close to the natural habitat conditions of T. sacculifer (S36, 26.5 ∘C; Fig. 3b, Appendix B). This corresponds to the lowest intra- and inter-test variability of ∼1.7 % measured on tests, which grew in situ in the open ocean before culturing started (see also Sect. 2.3).
3.2 Surface sediments
The ICP-OES-derived Na∕Ca values of T. sacculifer from both the Caribbean and Gulf of Guinea surface sediments match the results from single map analyses (electron microprobe) of chamber cross sections from cultured foraminifera (Figs. 4, 6a). All surface-sediment-related data are provided in Table 1.
Among all Caribbean stations, the surface water (0–60 m of water depth) salinity varies insignificantly by less than ±0.2 throughout the year (see Sect. 2.3, Fig. 1c). Temperature changes are also minor (with a maximum of ±0.3 ∘C at 0–60 m of water depth; Fig. 1d). Sediment surface foraminiferal Na∕Ca results in relation to salinity and temperature are shown in Figs. 4, 5, and 6a. Accordingly, all Na∕Ca values are presented with horizontal error bars. These indicate the salinity and temperature variations between 0 and 60 m water depths, representing the main habitat migration range of T. sacculifer (Sect. 2.1). As a result of minimal parameter changes with depth, horizontal error bars could be as small as their symbol sizes.
Maximum Na∕Ca values (5.68±0.3 mmol mol−1) were measured at stations SO164-7-3 and SO164-18-1 northwest of Haiti, showing the highest annual SSS at 30 m of water depth (∼36.3) for all sampling sites (Fig. 1a, c). The lowest Na∕Ca values of 4.64 and 4.79±0.2 mmol mol−1 were found southwest and southeast of Puerto Rico (stations SO164-23-3 and SO164-22-2), with an annual SSS of ∼35.4 at 30 m of water depth (Fig. 1a, c). In this respect, station SO164-24-3, which is close to the Puerto Rico stations, is exceptional as high Na∕Ca values of 5.51 mmol mol−1 were recorded at apparently low SSS (35.37). Nevertheless, a increase of about 0.2 mmol mol−1 per salinity unit is noticeable between the Puerto Rico stations and SO164-07-3/18-1.
All Caribbean stations exhibit Na∕Ca values within the error of the confidence interval of the Na∕Ca–salinity relationship derived from culture experiments (Figs. 4, 6a). This observation is also consistent with Na∕Ca values of in situ grown chambers in the open ocean (∼27.4 ∘C, ∼S35.7, WOA13) before culturing started (Fig. 6a, indicated by yellow reversed triangles). The Na∕Ca variability of averaged test concentrations (20–30 foraminifera per station) from Caribbean surface sediments varies between 5.5 % and 13 % in RSD (±0.2 to 0.7 mmol mol−1) among stations (Fig. 6a). These variations are consistent with results of single foraminifera analysis, as the inter-test variability indicates (salinity experiments: RSD of 5.5 %–6.5 %, mmol mol−1; temperature experiments: RSD of 3.2 %–11.5 %, –0.6 mmol mol−1) (Figs. 3, 4).
3.2.2 Gulf of Guinea
In contrast to the Caribbean, all sampling sites in the Gulf of Guinea are proximal to the Niger River mouth (Fig. 1b) with the upper 0–60 m being influenced by riverine freshwater input. Salinities vary from ∼32 to ∼35 at the surface and increase with water depth by 1.5–2 at stations close to freshwater discharge (GIK 16860-1, 16864-1, 16865-1) (Fig. 1c). Temperature variations at surface waters are minor (∼27–28 ∘C) compared to the significantly decreasing temperatures with water depth (0–60 m) by ∼27.5 to 19 ∘C (Fig. 1d). Na∕Ca results are therefore presented with horizontal error bars in order to account for the salinity (Figs. 4, 6) or temperature (Fig. 5) variations, respectively, in the preferred habitat depth (0–60 m) of T. sacculifer. Gulf of Guinea Na∕Ca results also lie within the 95 % confidence interval of our salinity culture experiments, even when taking into account their uncertainty marked by horizontal error bars (Fig. 6a). In comparison to the foraminiferal Na∕Ca variability of Caribbean surface sediments, samples from the Gulf of Guinea show the smallest Na∕Ca variability of ≤2 % (≤0.1 mmol mol−1) at all stations (Fig. 6a). The lowest Na∕Ca value of 4.77±0.03 mmol mol−1 in T. sacculifer was measured at station GIK 16865-1 close to the Niger and Sanaga river mouths with SSS of 35 at 30 m of water depth (Fig. 1b, c), while stations next to it at the same salinity level present higher Na∕Ca values ( mmol mol−1).
In the Gulf of Guinea temperature variations are higher ( ∘C) than changes in salinity with water depth and between sampling sites. Despite this, Na∕Ca values are in line with results of temperature culture experiments, demonstrating the limited impact of temperature on Na incorporation (Fig. 5).
3.2.3 Calcite dissolution effect on Na∕Ca in foraminiferal tests
Overall, Na∕Ca values of T. sacculifer from both Caribbean and Gulf of Guinea surface sediments show no significant correlation with increasing water depth, corresponding to the versus water depth profile at respective sampling stations (Table 1, Fig. 6b). Na∕Ca values of both sampling regions lie within the 95 % confidence interval (±0.25 mmol mol−1) of our salinity culture experiments (not affected by dissolution) and show the same range of inter-test variability (Figs. 4, 5 and 6a, Table 1).
In detail, although the onset of Mg∕Ca dissolution in planktonic foraminifera starts below the critical threshold of ∼21 µmol kg−1 (defined by Regenberg et al., 2006, 2014), stated at ∼3.5 km in the Caribbean, no similar trend is obvious from our foraminiferal Na∕Ca values at bottom waters until 4 km of water depth (Fig. 6b, Caribbean). Only three sampling stations (Caribbean: SO164-01-3, SO164-22-2, SO164-23-3) and their respective Na∕Ca values are below the critical threshold for Mg∕Ca dissolution, trending to a decline in Na∕Ca close to the calcite saturation horizon (∼4.7 km). Corresponding values of the latter stations show the lowest values of all Caribbean surface sediment samples. Although these Na∕Ca values do not intersect with any error bars of values above 4 km, they are still within the error of the 95 % confidence interval of cultured T. sacculifer (compare Fig. 6a and b).
Foraminiferal Na∕Ca values of Gulf of Guinea sediments show no clear trend versus (Fig. 6b). Compared to the Caribbean, the critical of ∼21 µmol kg−1 for Mg∕Ca dissolution (Regenberg et al., 2014) is already reached at 2.5–3 km of water depth in the Gulf of Guinea, but all stations are at supersaturated bottom waters >35 µmol kg−1 (Table 1) above 2.5 km. Further, the lowest Na∕Caforam value (GIK 16865-1) was measured in samples collected close to the Niger River discharge (Fig. 1b). Those samples were taken from the deepest station at this site (∼2.5 km of water depth; Table 1). Instead, both stations next to it (GIK 16860-1/16864-1) show higher Na∕Ca values ( mmol mol−1) collected at 0.2 and 1.5 km of water depth. Nevertheless, three of four stations show the same Na∕Caforam value of 4.92 mmol mol−1 between water depths of around 1.5 and 2.2 km, pointing to Na∕Ca values being unaffected by dissolution.
4.1 Inter- and intra-test variability
The inter- and intra-test element distribution revealed by high-resolution electron microprobe mapping provides important information on test Na∕Ca composition and heterogeneity, which is fundamental for proxy development. In this study, we explore the variability (expressed as RSD in percent) from averaged Na∕Ca electron microprobe maps within chamber wall cross sections of one foraminifer and among individual specimens. From our culture experiments the Na∕Ca inter- and intra-test variability varies between approximately 2 % and 16 % (Appendix B). This is in line with previous studies reporting an inter-test variability of 9 %–17 % (RSD) measured by laser ablation ICP-MS (Wit et al., 2013; Mezger et al., 2016).
Compared to the Mg∕Ca variability (≥30 %) observed in symbiont-bearing foraminiferal species, the Na∕Ca inter-test variability of T. sacculifer is relatively low, half that determined for Mg∕Ca (Sadekov et al., 2005; Dueñas-Bohórquez et al., 2011). Previous studies on (trace) metal distribution in various species of planktonic foraminifera showed, for instance, prominent Mg∕Ca banding alternating in high and low Mg–calcite bands within chamber walls. These variations are likely linked to different calcification mechanisms, with the inner primary calcite enriched in Mg and the outer thickening calcite depleted (together named as ontogenetic calcite) (Erez, 2003; Eggins et al., 2003; Sadekov et al., 2005; Dueñas-Bohórquez et al., 2011; Hathorne et al., 2009; Spero et al., 2015). Potential factors controlling Mg∕Ca values in banding, which could change the biological activity of foraminifera and/or their symbionts, are changes in calcification temperatures (due to habitat migration or seasonal change), seawater pH, pH in the calcifying microenvironment, carbonate ion concentrations, or diurnal day–night cycles (Eggins et al., 2004; Sadekov et al., 2005; Dueñas-Bohórquez et al., 2011; Spero et al., 2015; Davis et al., 2017; Fehrenbacher et al., 2017).
These potential factors affecting Mg heterogeneity could also bias Na incorporation. In the following, the possible effects on Na∕Ca inter- and intra-test variability are discussed. The reduced Na∕Ca variability compared to higher Mg∕Ca variations implies less pronounced Na∕Ca banding as found for Orbulina universa (Branson et al., 2016) and possible differences in calcification pathways (e.g., ion transport mechanisms to the calcification site in the cell). Using time-of-flight secondary ionization mass spectrometry, only one fine band (<500 nm) enriched in Na was found in all specimens, identified close to the primary organic sheet where the spines of foraminifera grow according to Branson et al. (2016). This is consistent with observations from Erez (2003), who reported higher Na concentrations in benthic foraminifera in proximity to the primary organic sheet, located between the inner and outer calcite. Branson et al. (2016) demonstrated that Na is not associated with higher Mg concentrations within tests of Orbulina universa, which could also be valid for T. sacculifer and other planktonic species.
Nevertheless, although the high Mg variability (>30 %) is strongly biologically controlled, changes in ambient environmental conditions, such as temperature or salinity, could also bias Mg∕Ca values in foraminifera (Nürnberg et al., 1996; Bentov and Erez, 2005, 2006; Dueñas-Bohórquez et al., 2009). Transferred to our study, higher Na∕Ca intra-test variations within single wall cross sections of each salinity and temperature experiment (Appendix B) may occur due to possibly higher ecological stress levels of (individual) foraminifera in culture. This hypothesis, which would imply a strong dependence of Na incorporation on environmental changes, is supported by the appearance of the lowest Na∕Ca range in tests which grew at culture settings close to the natural habitat of T. sacculifer (26.5 ∘C, S36) (Fig. 3).
The inhibition of chamber formation or gametogenesis, as observed in cultured foraminifera at different salinities (Bijma et al., 1990b), may be a prime indication of the biological response of foraminifera to environmental stress. Only within one culture experiment at a salinity of 41 did foraminifera precipitate more than two to three new chambers, while only one additional chamber grew at salinities below and above 41. Precipitation of gametogenic calcite (GAM) was only observed at salinity experiments of S44. Compared to salinity culture experiments, foraminifera were able to precipitate three to four new chambers in all temperature experiments (Hemleben et al., 1987; Bijma et al., 1990b; Nürnberg et al., 1996).
At the end of their life cycle foraminifera precipitate gametogenic calcite below their averaged living depth and commonly cooler waters, which should result in calcite with lower Mg∕Ca values (Nürnberg et al., 1996; Erez, 2003; Sadekov et al., 2005; Rebotim et al., 2017). In the culture experiments, the rate of gametogenesis was significantly influenced by salinity. As shown in different culture experiments of Bijma et al. (1990b), around 40 % of foraminifera successfully underwent gametogenesis at salinities between 41 and 44, but the reproduction frequency decreases ∼10-fold above a salinity of 45. However, Nürnberg et al. (1996) already noted that GAM calcite, when secreted at the same temperatures, is enriched in Mg relative to ontogenetic calcite because their biomineralization mechanisms could be fundamentally different (Bentov and Erez, 2006; Hamilton et al., 2008). Hamilton et al. (2008) proposed different calcification processes in the microenvironment of foraminifera prior to the gamete formation compared to the calcite precipitation of ontogenetic calcite (see Sect. 4.4). Similarly, our study points to geochemical differences between GAM and ontogenetic calcite with reduced Na∕Ca values in GAM calcite at a salinity of 44 (Figs. 3, 4). This agrees with findings that the outer gametogenic calcite layer has lower Mg∕Ca values (e.g., Brown and Elderfield, 1996; Hathorne et al., 2003; Sadekov et al., 2005). Although we could show differences between GAM and ontogenetic calcite, it needs to be considered in this respect that foraminifera cultured in the laboratory do not migrate to depth while they precipitate GAM calcite, as foraminifera do in the field (Bé, 1980, Hemleben et al., 1989; Erez, 2003).
4.2 Na∕Ca as a proxy for salinity
For T. sacculifer, Na incorporation increases significantly (p<0.005) by 2.25 % per salinity unit during culture experiments () (our study, Fig. 4). Within each experiment Na∕Ca values are normally distributed (Shapiro–Wilk test; Appendix A). Our results are broadly consistent with previous culture studies (Fig. 7), showing a positive correlation between Na∕Ca and seawater salinity for the benthic foraminifer Ammonia tepida and increasing Na∕Ca by 3 % per salinity unit (Wit et al., 2013). Allen et al. (2016) observed a Na∕Ca increase of 1 % per salinity unit in cultured G. ruber (pink), while there was no such salinity relationship in their T. sacculifer over a salinity range from 33 to 40 (Fig. 7). As the slope of the Na∕Ca versus salinity regression appears steeper for G. ruber than for T. sacculifer, Allen et al. (2016) suggested that the sensitivity of Na incorporation in response to salinity change is species specific and higher for G. ruber. Conversely, no differences were observed in Na∕Ca values between G. ruber and T. sacculifer within the field calibration study from the Red Sea (Mezger et al., 2016; Fig. 7). In that study Na∕Ca values were also markedly higher compared to Wit et al. (2013) and Allen et al. (2016) (Fig. 7). Na∕Ca increases by ∼7.5 %–8 % per salinity unit in G. ruber (w) and T. sacculifer, respectively (Mezger et al., 2016). The authors attributed this deviation to region-specific environmental and oceanographic conditions compared to the open ocean (Mezger et al., 2016; see detailed discussion in Sect. 4.3). Overall, this demonstrates the necessity for establishing species-specific (and regionally dependent) calibrations, similar to foraminiferal Mg∕Ca paleothermometry.
With respect to paleosalinity reconstructions, our results from culture experiments and surface sediment samples indicate that foraminiferal Na∕Ca may serve as a direct proxy for ocean salinities, but has limitations, as listed below. We demonstrate for cultured T. sacculifer that a change of ±1 salinity unit results in a Na∕Ca change of 2.25 %, i.e., ±0.12 mmol mol−1 in absolute terms. This change definitely exceeds the analytical uncertainty of the electron microprobe and the ICP-OES measurements (0.2–0.4 % RSD), providing the ability to resolve past SSS changes of this magnitude. Although the intra- and inter-test Na∕Ca variability of cultured T. sacculifer shown here is up to 10 times higher (Sect. 4.1) than the absolute change per salinity unit, averaged Na∕Ca values of specimens for each treatment fit with the Na∕Ca–salinity calibration and lie within the 95 % confidence interval (Fig. 4). The respective average Na∕Ca uncertainties, expressed as the standard error (SE), vary between ∼0.05 and 0.37 mmol mol−1 per salinity condition, which would correspond to a minimum salinity sensitivity of 0.14 units (Appendix C). As already demonstrated for Mg∕Ca, which has a strong intra- and inter-test heterogeneity, the deviation from the mean would decrease as the number of total specimens used for analyses increases (Sadekov et al., 2008; De Nooijer et al., 2014a). To resolve a salinity change of 0.1 (SE: 0.036 mmol mol−1), 40 to 50 specimens are statistically necessary based on our Na∕Ca–salinity calibration (Appendix C). Sodium is known to be heterogeneously distributed in foraminiferal calcite (Branson et al., 2016) and Na∕Ca intra- and inter-test heterogeneity is also observed here with single electron microprobe maps on chamber wall cross sections within one specimen having a standard error of 0.08–0.61 mmol mol−1. The latter standard error corresponds to a minimum salinity sensitivity of ∼0.7 units. To resolve a salinity change of 0.1 (SE: 0.01 mmol mol−1) with single spot analysis on one specimen, 30–60 measurements (S26–36) or up to 80 measurements (>S41) are required (Appendix C). The inter-test heterogeneity of Na∕Ca in cultured T. sacculifer observed here is rather low (∼5.5–6.5 RSD % for salinity experiments) compared to the inter-test variability of ∼14 RSD % observed by Mezger et al. (2016) (see Sect. 4.1). Since we exclusively analyzed chamber walls and avoided measuring other parts of the test with a distinct morphology and (potentially) different chemical composition (e.g., GAM calcite, crust, spines), Na∕Ca may be more variable than reported here. Nonetheless, the Na∕Ca range between single foraminifera of all culture experiments measured by the electron microprobe (±0.17–0.6 mmol mol−1) is rather similar to that averaged from 20–30 T. sacculifer specimens (which all have various amounts of gametogenic calcite) measured by the ICP-OES (Caribbean surface sediment samples: ±0.18–0.56 mmol mol−1, Gulf of Guinea surface sediment samples: ±0.03–0.14 mmol mol−1) (Figs. 4, 6a). Both field studies suggest at least 20 specimens are necessary to resolve past salinity changes of 0.5 to 1 (SE: 0.18–0.36 mmol mol−1; Appendix C).
With a sensitivity of 0.5 salinity units, reconstructions of paleoriver discharge (see, e.g., Weldeab et al., 2007) as well as glacial meltwater discharge (e.g., in Flower et al., 2004) should become possible, independent of stable oxygen isotope approaches. Therefore, the application of Na∕Caforam in multi-proxy approaches, as already suggested in Vetter et al. (2017) to combine, e.g., foraminiferal with Ba∕Ca, could provide more confidence to such reconstructions by providing absolute salinity values instead of previous indirect estimations.
4.3 The reliability of the foraminiferal Na∕Ca–salinity proxy
4.3.1 Temperature effect on Na incorporation
Before accepting Na∕Ca as a robust paleoceanographic tool, factors other than salinity potentially affecting Na incorporation need to be quantified. The statistically insignificant correlation of Na∕Ca with temperature changes in cultured T. sacculifer in our study (Figs. 3, 5) is in agreement with results reported by Allen et al. (2016) (Fig. 8). In contrast, the Red Sea plankton pump study of Mezger et al. (2016) showed a negative correlation between Na∕Ca values and temperature for G. ruber (R2=0.84, p<0.001) and T. sacculifer (R2=0.95, p<0.001) (Fig. 8). It is important to note that increasing temperatures (∼26–29 ∘C) in these samples are paralleled by decreasing salinities (from ∼40 to 37; Mezger et al., 2016, Fig. 8) and possibly other factors, such as changes in carbonate chemistry, in the Red Sea. Therefore, it was not possible to separate effects from each other. The absence of a temperature effect on Na incorporation in foraminiferal tests shown here would suggest that the apparent correlation observed by Mezger et al. (2016) was probably not due to temperature. A putative impact of the extreme salinity in the Red Sea can also be disregarded as the culture study here extended even beyond the very high salinities found in the Red Sea (45 versus 41).
Although T. sacculifer prefers higher temperatures (optimum 28 ∘C) and is mostly absent below 23 ∘C (Žarić et al., 2005), Na∕Caforam changes are minor in our study within temperature changes (19.5–29.5 ∘C) (Fig. 3b). Hence, there is quite robust support that variations in foraminiferal Na∕Ca are not primarily driven by temperature.
4.3.2 Further potential factors controlling Na incorporation
Although temperature shows no statistically significant relationship with foraminiferal Na∕Ca, aberrant Na∕Ca values between the same and amongst other planktonic and benthic foraminiferal species need to be discussed. Beside salinity as the potential dominant factor controlling Na incorporation into calcite tests, changes in seawater carbonate chemistry, biological processes, different sample preparation techniques, and/or diagenetic altering of fossil tests may affect the geochemical signature of foraminifera, which will be discussed below.
Averaged Na∕Ca values of cultured T. sacculifer (our study) are lower by ∼1–2 mmol mol−1 than those reported for A. tepida in Wit et al. (2013) and G. ruber and T. sacculifer in Allen et al. (2016) for the overlapping salinity interval of 30 to 38 in culture experiments (Fig. 7). Foraminiferal samples from the Red Sea are even higher by up to 4 mmol mol−1, with Na∕Ca values of 7–14 mmol mol−1 (±2–6 mmol mol−1) in G. ruber (white) and T. sacculifer within the salinity range of 37–40 (Mezger et al., 2016; Fig. 7). Mezger et al. (2016) related the extremely high Na∕Ca values to many covarying factors (e.g., carbonate chemistry, salinity, temperature) in the Red Sea, which may differ from open ocean conditions. Increasing dissolved inorganic carbon (DIC), pH, and the calcite saturation state () are likely promoting higher calcite precipitation rates and hence the uptake of trace elements, as observed for cultured benthic foraminifera (Bentov et al., 2009; De Nooijer et al., 2014b). Beside that, Allen et al. (2016) did not note a significant relation of Na∕Ca with (or pH) and DIC concentration and could not see a clear relationship between trace element partitioning and calcification rates in G. ruber (pink) and T. sacculifer. Hence, they assumed that calcification rates are not important factors for Na+ incorporation (Allen et al., 2016). This could indicate that differences in Na∕Ca within one species could be region specific due to indirect environmental controls on Na incorporation.
Although changes in seawater pH probably have a negligible effect on Na incorporation (Allen et al., 2016), pH changes in the microenvironment of foraminiferal tests, which are mainly regulated or biased by the photosynthetic activity of their symbionts, could impact Na variations instead. The symbiont activity depends on nutrient concentrations and light intensities and can thus actively change the pH of the ambient microenvironment (Rink et al., 1998; Wolf-Gladrow et al., 1999). Higher photosynthetic rates can thereby influence the test geochemistry, which has been demonstrated by boron isotopes in symbiont-bearing species, such as T. sacculifer and O. universa (Hönisch et al., 2003; Allen et al., 2011). In contrast, the Mg∕Ca heterogeneity of these species is neither related to seawater pH (Dueñas-Bohórquez et al., 2011) nor microenvironment pH changes due to symbiont photosynthetic–respiration activity and instead is linked to the diurnal day–night cycles (Spero et al., 2015). Hence, as Na incorporation is presumably not affected by pH () (Allen et al., 2016), other factors are influencing the Na variability. The inter- and intra-specimen variations of Na∕Ca in the calcite tests may be related to the active biological control on Na+ incorporation during different biomineralization processes causing ontogenetic variations, as described extensively for Mg∕Ca in previous studies (Erez, 2003; Bentov and Erez, 2006; De Nooijer et al., 2014b) (see Sect. 4.4 for a detailed discussion).
However, all factors mentioned previously do not explain the differences in the amount of Na∕Ca in T. sacculifer between our study and Allen et al. (2016), especially since specimens for both studies were collected in the Caribbean for culture experiments. We assume that the absolute Na∕Ca difference could be related to different cleaning techniques applied prior to analyses, which would need to be confirmed and quantified by additional experiments. The preparation for analysis is essential as has been exemplarily demonstrated by Rosenthal et al. (2004) for foraminiferal Mg∕Ca and its reference materials. Furthermore, observed differences could also be explained by different measurement approaches. The studies of Allen et al. (2016) and Mezger et al. (2016) provided a mixed Na∕Ca signal by measuring the entire newly calcified chamber during culture (including ontogenetic, gametogenic calcite, and/or spines), while we took care to avoid parts of the test with a distinct morphology and (potentially) different chemical composition. The wet chemical Na∕Ca analyses (ICP-OES) with 20 to 30 specimens per surface sediment sample (Caribbean, Gulf of Guinea) match the single foraminiferal analyses by electron microprobe (Figs. 4, 6), which further supports the representativeness of our data.
In addition to the parameters discussed above, which could affect and regulate Na+ incorporation in living foraminifera, we also need to address the preservation state of sodium in the tests over time. It is widely accepted that early diagenetic processes can significantly alter the geochemical composition of fossil foraminifera. For instance, planktonic foraminiferal Mg∕Ca values start to decline linearly below the critical threshold of ∼21.3 µmol kg−1 (Regenberg et al., 2006, 2014; see Sect. 2.3 for details). Evidently, we cannot see the same trend for values from Caribbean surface sediments, although Na∕Ca seems to decline at 3.5 to 4 km of water depth below a level of <13 µmol kg−1 (Fig. 6b). In the Gulf of Guinea, the critical threshold value is at even shallower water depth (∼2.5 km), but no significant Na∕Ca change with water depth is obvious, matching the Caribbean values (Table 1, Fig. 6b). Therefore, Na∕Ca seems to be less affected by dissolution than Mg∕Ca, which could be linked to different incorporation mechanisms of both elements into foraminiferal calcite (see Sect. 4.4). The issue of Na∕Ca removal due to calcite dissolution at greater water depth nonetheless needs further investigation because of the limited sample set of our study.
Although the calcite saturation state is quite different in bottom waters and differs regionally in depth (Brown and Elderfield, 1996; Dekens et al., 2002; Regenberg et al., 2006, 2014), we suspect that foraminiferal Na∕Ca, similar to foraminiferal Mg∕Ca dissolution, does not change above the critical calcite saturation state of µmol kg−1 in the Caribbean and the Gulf of Guinea at least over the last ∼3000 years (ages of Caribbean and Gulf of Guinea surface sediments; Regenberg et al., 2009). Although the lowest Na∕Ca values of surface sediments are possibly affected by calcite dissolution at respective water depths below 3.5 km, all foraminiferal Na∕Ca values match the 95 % confidence interval of culture experiments not affected by dissolution (Figs. 4, 6a). This confirms the robustness of Na∕Ca as a paleosalinity proxy over time.
4.4 Incorporation of Na+ in foraminiferal calcite
The high variations of Na∕Ca between and within benthic and planktonic species (Fig. 7), and the heterogeneity within chamber walls, suggest a biological control of Na+ incorporation during calcification. To examine this hypothesis, the apparent partition coefficient for Na in organic or inorganic calcite is expressed as in mmol mol−1. Partition calculations are based in our study on mol mol−1 as given in Delaney et al. (1985). Foraminifera in Delaney et al. (1985) were collected from the same sampling site as the cultured specimens of our study. In our study DNa of T. sacculifer is DNa=0.11–, which is in agreement with previously reported DNa: Allen et al. (2016) for T. sacculifer, G. ruber: ; Wit et al. (2013) for A. tepida: DNa=0.12–; Delaney et al. (1985) for T. sacculifer: DNa=0.14–. The highest partition coefficient was found in the Red Sea field calibration study from Mezger et al. (2016) for G. ruber and T. sacculifer with DNa of 0.18–. Notably, in inorganic calcite the partitioning of Na varies between DNa=0.3 and (Busenberg and Plummer, 1985; White, 1978) and is therefore markedly higher compared to foraminiferal calcite. The generally 2 times lower foraminiferal DNa values compared to inorganic calcite suggest a biological control on Na incorporation in foraminiferal calcite, as it is also known for Mg incorporation (e.g., Bentov and Erez, 2006; De Nooijer et al., 2014b). The partition coefficient of Mg in planktonic foraminiferal calcite (e.g., DMg (T. sacculifer, G. ruber) = ∼0.7– in Allen et al., 2016; DMg (O. universa) = 0.002 in Lea et al., 1999) could be 5 to 10 times lower than observed for inorganic precipitated calcite (0.01) (Busenberg and Plummer, 1989). Additionally, Mg∕Caforam increases by 8 %–10 % per ∘C, and only 3 % per ∘C in inorganic calcite, demonstrating a strong biological control over any kinetic and thermodynamic influence on test Mg incorporation (Nürnberg et al., 1996; Lea et al., 1999; Allen et al., 2016). Recent results of Allen et al. (2016) show an increase in DMg with increasing calcification rates, but not for DNa of T. sacculifer and G. ruber. This supports the assumption of a biological control on Na incorporation, as Busenberg and Plummer (1985) report increasing Na∕Ca values with increasing calcite growth rates of inorganic calcite, thought to result from increasing lattice distortions providing space for Na incorporation.
It is known from previous studies that perforate foraminifera are able to control the elemental composition of their calcite tests regulated in the microenvironment of their cells (Erez, 2003; Bentov and Erez, 2006; De Nooijer et al., 2014b). Different calcification pathways could possibly bias the element transport to the calcification site via various transport mechanisms, which could affect Na+ incorporation. There are different mechanisms proposed from which the ions needed for the calcification process derive. The first model of Erez (2003) suggested the uptake of ambient seawater transported and modified via vacuoles into the cell, from which the calcification starts. Alternatively, the ions taken up by seawater vacuolization may be stored in intracellular reservoirs before being used during calcification (Bentov and Erez, 2006; De Nooijer et al., 2014b). Foraminifera are also able to directly uptake ions from the ambient seawater by using a selective ion transport via ion pumps or channels during calcification. Just considering transport systems with Na+ involved, the most abundant mechanism is a exchanger that specifically counter transports one Mg2+ ion across the lower gradient into the cell, in exchange with 2Na+ ions (Bentov and Erez, 2006). On the other hand, Mg2+ ions could also be removed from the parent solution in the cell via transmembrane channels using the electrochemical gradient, which is generated by a or antiporter. These antiporters basically regulate the pH of the calcifying fluid and hence increase calcite precipitation (Erez, 2003; Bentov and Erez, 2006; De Nooijer et al., 2009; Toyofuku et al., 2017). In conclusion, Na+ ions potentially have an important function for element incorporation and calcification processes in the cell of perforate foraminifera, which could strongly influence Na partitioning. Hence, biomineralization processes could be fundamentally different between species (Bentov and Erez, 2006; De Nooijer et al., 2014b).
The next unknown in this process is the incorporation mechanism of Na in calcite. Due to the similar size of the ionic radii of both Na+ and Ca2+, Yoshimura et al. (2017) suggested that Na is likely to directly substitute for calcium ions as well as other divalent cations like Mg2+ or Sr2+ in spite of the difference in charge. In this case, two Na+ ions paired with anion vacancies (e.g., generated by ) as a possible charge compensator would replace two Ca2+ ions (White, 1977). Alternatively one Na+ ion accompanied by anions such as Cl− or , which induce calcite lattice distortions, would replace Ca2+ and ions (Yoshimura et al., 2017). However, this incorporation mechanism is only described for inorganic precipitation experiments of aragonites so far, in which alkali metals (e.g., Na+, K+, or Li+) directly substitute for Ca2+, whereas alkali metals occupy interstitial positions in inorganic calcite lattice defects due to a different crystal structure (Ishikawa and Ichikuni, 1984; Okumura and Kitano, 1986). This may play a role in the different Na contents of biogenic calcite, such as foraminifera (Na: ∼1000 ppm, Na∕Ca: ∼5 mmol mol−1), and aragonite, such as corals (Na: ∼5000 ppm, Na∕Ca: ∼20 mmol mol−1) (Yoshimura et al., 2017).
Despite the likelihood that Na is not competing with Ca for lattice sites, Wit et al. (2013) suggested that Na+ incorporation into foraminiferal calcite is mainly driven by the activity ratio of free Na+ to free Ca2+ in seawater, which is related to their concentrations in seawater and increases with salinity (Ishikawa and Ichikuni, 1984; Zeebe and Wolf-Gladrow, 2001). In contrast, Na+ and Ca2+ activities in seawater are only affected by temperature changes to a limited extent, and hence temperature has a minimal influence on Na incorporation (Ishikawa and Ichikuni, 1984; Delaney et al., 1985; Zeebe and Wolf-Gladrow, 2001). Instead, lower temperatures could cause enhanced solubility of calcium carbonate, resulting in an increase in free Ca2+ (Zeebe and Wolf-Gladrow, 2001). This could induce lower Na∕Ca values in foraminiferal calcite at higher temperatures and would explain the slight, but insignificant, negative response of Na∕Caforam to temperature.
Foraminiferal Na∕Ca of cultured T. sacculifer correlates positively (R=0.97, p<0.005) with increasing sea surface salinity between 26 and 45 salinity units: salinity = (). A temperature control on Na incorporation in foraminiferal calcite can be excluded by our data, supporting previous culture studies (Allen et al., 2016). In our experiments, we observed a rather low Na∕Ca inter- and intra-test variability of around 2 %–16 %, half of that determined for Mg∕Ca (≥30 %) in symbiont-bearing foraminiferal species (Sadekov et al., 2005; Dueñas-Bohórquez et al., 2011). The reduced Na∕Ca variability compared to higher Mg∕Ca variations implies less pronounced Na∕Ca banding. As a relationship between neither Na partitioning and calcification rates nor changes in the carbonate chemistry (pH, (), DIC) was observed in foraminiferal calcite (Allen et al., 2016), there is quite robust support for the fact that variations in Na∕Caforam are primarily driven by salinity.
According to our culture studies, a change of ±1 salinity unit would result in a Na∕Ca change in T. sacculifer calcite of 2.25 %, equivalent to ±0.12 mmol mol−1. This is in agreement with Na∕Ca values of T. sacculifer selected from both Caribbean and Gulf of Guinea surface sediments. We observed no significant calcite dissolution effect on Na∕Ca in foraminiferal calcite with changes in the calcite saturation state above 2.5 km of water depth in the Gulf of Guinea and 3.5 to 4 km in the Caribbean, while Na∕Ca values decline below. However, Na∕Ca does not change above the critical threshold of ∼21 µmol kg−1 established for the onset of Mg∕Ca dissolution in planktonic foraminifera (Regenberg et al., 2006, 2014). Further, Na∕Ca values of surface sediment samples lie within the 95 % confidence interval of our salinity culture experiments, which are unaffected by calcite dissolution. Therefore, our new data support the fact that foraminiferal Na∕Ca potentially serves as a direct and reliable proxy for significant changes in ocean salinities, e.g., exceeding 0.5 salinity units.
However, the sensitivity of Na∕Ca to salinity changes is species specific and possibly regional dependent, as demonstrated by the offset of 1–3 mmol mol−1 between various planktonic and benthic species, suggesting a dominant biological control (Wit et al., 2013; Allen et al., 2016). Further improvement and proxy development could be achieved by a multi-proxy approach, e.g., combining Na∕Ca paired with Mg∕Caforam, δ18Osw and Ba∕Caforam, to support the confidence of past salinity reconstructions.
The sample material used is archived at the GEOMAR Helmholtz Centre for Ocean Research Kiel (contact: email@example.com). All data used in this study are listed in the paper and the appendices.
JBe and DN designed this study. Data analyses and preparation of the paper were carried out by JBe with assistance from DN and ECH. The culture experiments described in this study were carried out by JBi. Measurements of Gulf of Guinea foraminiferal samples were accomplished by SN. GJR, EMM, LJdN, ECH, JS, JBi, and MK contributed to data interpretation and significantly improved the paper with intense discussions and text iterations.
The authors declare that they have no conflict of interest.
We gratefully thank Jan Fietzke, Mario Thöner, Thor Hansteen, and
Nicolaas Glock for their technical support and improving measurement
techniques for the electron microprobe at GEOMAR Helmholtz Centre for Ocean
Research Kiel. Special thanks go to Nadine Gehre for assistance in the
laboratory. We benefited from the comments of two anonymous reviewers, which greatly improved
the paper. Gert-Jan Reichart and Lennart de Nooijer acknowledge NESSC
funding. Jacqueline Bertlich was funded by a PhD fellowship of the Helmholtz
Research School for Ocean System Science and Technology (HOSST) at GEOMAR
Helmholtz Centre for Ocean Research Kiel (VH-KO-601).
The article processing charges for this open-access
publication were covered by a Research
Centre of the Helmholtz Association.
Edited by: Aninda Mazumdar
Reviewed by: two anonymous referees
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