Global ocean dimethyl sulfide climatology estimated from observations and an artificial neural network
Marine dimethyl sulfide (DMS) is important to climate due to the ability of DMS to alter Earth's radiation budget. Knowledge of the global-scale distribution, seasonal variability, and sea-to-air flux of DMS is needed in order to improve understanding of atmospheric sulfur, aerosol/cloud dynamics, and albedo. Here we examine the use of an artificial neural network (ANN) to extrapolate available DMS measurements to the global ocean and produce a global climatology with monthly temporal resolution. A global database of 82 996 ship-based DMS measurements in surface waters was used along with a suite of environmental parameters consisting of latitude–longitude coordinates, time of day, time of year, solar radiation, mixed layer depth, sea surface temperature, salinity, nitrate, phosphate, and silicate. Linear regressions of DMS against the environmental parameters show that on a global-scale mixed layer depth and solar radiation are the strongest predictors of DMS. These parameters capture ∼9 % and ∼7 % of the raw DMS data variance, respectively. Multilinear regression can capture more of the raw data variance (∼39 %) but strongly underestimates DMS in high-concentration regions. In contrast, the artificial neural network captures ∼66 % of the raw data variance in our database. Like prior climatologies our results show a strong seasonal cycle in surface ocean DMS with the highest concentrations and sea-to-air fluxes in the high-latitude summertime oceans. We estimate a lower global sea-to-air DMS flux (20.12±0.43 Tg S yr−1) than the prior estimate based on a map interpolation method when the same gas transfer velocity parameterization is used. Our sensitivity test results show that DMS concentration does not change unidirectionally with each of the environmental parameters, which emphasizes the interactions among these parameters. The ANN model suggests that the flux of DMS from the ocean to the atmosphere will increase with global warming. Given that larger DMS fluxes induce greater cloud albedo, this corresponds to a negative climate feedback.
Dimethyl sulfide emitted from the surface ocean is the major precursor for aerosol sulfate in the marine atmosphere. These aerosols play a significant role in the climate system both directly, through aerosol radiative effects, and indirectly, through their role as cloud condensation nuclei and influence on cloud radiative properties (Andreae and Rosenfeld, 2008). Assessing the impact of dimethyl sulfide (DMS) on global climate requires an understanding of the seawater DMS distribution and the factors controlling variability on a variety of spatial and temporal scales. Dimethyl sulfide is produced in surface waters, mainly via enzymatic cleavage of the biogenic compound dimethyl sulfoniopropionate (DMSP; Stefels et al., 2007). The abundance of DMS in surface waters is a function of numerous factors controlling production and loss rates, as well as pathways of both DMSP and DMS (Simó, 2001; Toole and Siegel, 2004; Galí et al., 2015). Developing mechanistic and predictive models of surface ocean DMS is challenging due to limitations of the existing observational database and process rate measurements.
Given the biogenic origin of DMS, early efforts focused on the relationship between DMS and Chl a (a proxy for biomass). Positive correlations between DMS and Chl a have been reported on basin scales (e.g., Andreae and Barnard, 1984; Yang et al., 1999). However, this positive correlation disappears when more data are used. Kettle et al. (1999) found no significant relationship between DMS and Chl a based on the global DMS dataset available at the time. The weak relationship may be caused by the so-called “summer DMS paradox”, which describes a phenomenon in which the annual maximum of the surface DMS concentration is commonly detected in summer when Chl a is at its annual minimum in midlatitude and subtropical low-latitude waters (Simó and Pedrós-Alió, 1999). Kettle et al. (1999) also tested linear regression models on a compilation of data, including sea surface salinity and temperature, nitrate, silicate, phosphate, and Chl a. The authors then concluded that no simple algorithm based on linear regression could be used to create monthly DMS fields, indicating that more complex mechanisms can control surface DMS concentrations.
Simó and Dachs (2002) achieved a strong linear relationship between heavily binned/averaged DMS and mixed layer depth (MLD) when Chl a ∕ MLD ≥ 0.02, as well as a logarithmic relationship between DMS and Chl a ∕ MLD when Chl a ∕ MLD < 0.02. Vallina and Simó (2007) found a linear relationship between DMS concentration and solar radiation dose (SRD) in the coastal northwestern Mediterranean. They conducted a global-scale study by dividing the ocean into 10∘ latitude by 20∘ longitude boxes and correlating SRD and the box-averaged DMS concentration. A strong linear relationship was detected in this filtered dataset. Derevianko et al. (2009) reexamined the relationship between SRD ∕ MLD and DMS concentration by using 1∘ by 1∘ bins and found that only a small fraction (14 %) of the DMS variance was captured by a linear model based on SRD or MLD. These authors also pointed out that the previously identified strong relationship between MLD ∕ SRD and DMS “results from the reduction in the total variance in the data due to binning” (Derevianko et al., 2009).
Prognostic models have also been used to obtain climatological DMS distributions. In these models, phytoplankton are divided into different groups based on their ability to produce DMSP, the precursor of DMS. For example, diatoms produce less DMS than coccolithophores and Phaeocystis (e.g., Bopp et al., 2003; Vogt et al., 2010; Gypens et al., 2014). Elliott (2009) implicitly incorporated Phaeocystis in a model by assuming that DMS yields are simply related to temperature. The work of Wang et al. (2015) explicitly incorporated Phaeocystis into the Biogeochemical Elemental Cycling (BEC) model and included DMSP production from each phytoplankton group, along with DMS leakage pathways from algal cells (grazing, lysis, and exudation). Despite this level of modeling detail, there are still large discrepancies between the model simulations and in situ measurements (Tesdal et al., 2016). Le Clainche et al. (2010) suggested that environmental conditions should be included in future model development because DMS cycling depends strongly on phytoplankton dynamics.
The DMS climatologies used in most climate models were obtained by extrapolating observed DMS to the global ocean using objective analysis schemes (Kettle et al., 1999; Lana et al., 2011). In those climatologies, observational data were first binned and averaged into 1∘ by 1∘ grid squares, which were then grouped into 57 static biogeographic provinces according to Longhurst (2007). Many provinces lacked adequate data to create a reliable climatology (Fig. A1 in the Appendix). In those situations, they first generated an annual cycle with monthly means for each province. Temporal interpolations were used to fill the monthly gaps if there were enough data to create a robust annual mean. Otherwise, weighted interpolation from neighboring provinces was used to fill the remaining gaps. Major gaps remain in the observational database for wintertime in the high latitudes of both hemispheres.
Machine learning is being increasingly used in oceanography and geoscience studies (Bergen et al., 2019). For example, Roshan and DeVries (2017) applied an artificial neural network (ANN) to extrapolate observed dissolved organic carbon (DOC) to the global ocean. Rafter et al. (2019) used an ensemble of neural networks to study oceanic δ15N distribution. ANNs have also been used to study DMS on regional scales (e.g., Humphries et al., 2012). The popularity of machine learning partially stems from one of its inherent advantages: it can detect nonlinear relationships that traditional linear regression models are unable to capture. In this study, we explore the relationships between DMS and environmental parameters using a machine-learning method. Such relationships are hard to detect using traditional linear regression methods, because environmental parameters do not directly influence DMS concentration. They control the distribution of marine algae that determines the distribution of DMSP (a precursor of DMS) and its conversion to DMS (Kiene et al., 2000; Simó, 2001). The objective of this paper is to discover the relationships between DMS and environmental variables, with the goal of constructing a novel monthly-resolved DMS climatology.
The paper is organized as follows. We begin by exploring the relationships between DMS concentration and various environmental parameters taken one at a time using linear regression. We then do a stepwise multilinear regression to create a reference model to which we compare our neural network model results. Lastly, we train an ANN using DMS measurements and environmental parameters. With the trained networks, we extrapolate the sparse measurements globally to obtain gridded fields of monthly DMS distributions and sea-to-air DMS fluxes.
2.1 Data sources and cleaning
Surface ocean DMS data were obtained from the Global Surface Seawater DMS Database (Pacific Marine Environmental Laboratory, PMEL; last access: 1 May 2020) and from the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) (Behrenfeld et al., 2019) (Table A1). In total, there are 93 571 valid measurements (PMEL: 86 785; NAAMES: 6786) after removing ultralow (<0.1 nM) and ultrahigh (>100 nM) DMS measurements according to Galí et al. (2015). The number of measurements used are substantially more than the 47 313 used by Lana et al. (2011). The Global Surface Seawater DMS Database also includes some ancillary in situ data, such as DMSP (4620), Chl a (PMEL: 11 491; NAAMES: 6750), sea surface temperature (SST; PMEL: 81 069; NAAMES: 6786), and salinity (SSS; PMEL: 77 209; NAAMES: 6786). In situ SST and SSS were used if available. If not, monthly climatology data from other sources (Table A1) were used to fill the gaps. SeaWiFS Chl a data (monthly average, Level 3-binned, spatial resolution of 9.2 km, last access: 1 May 2020) from December 1997 to March 2010 were matched to DMS data according to coordinates and sampling date. We compared PMEL in situ Chl a to SeaWiFS Chl a, which are well correlated on a logarithmic scale (R2=0.64) with a slope of 0.67 and an intercept of −0.06, , which means that on a logarithmic scale SeaWiFS Chl a concentrations are on average ∼30 % lower than those of in situ Chl a concentrations. This is possibly because SeaWiFS Chl a is calibrated based on high-performance liquid chromatography (HPLC)-determined Chl a (Morel et al., 2007), which on average is ∼40 % lower than that determined using the fluorometric method (Sathyendranath et al., 2009). Unfortunately, there is no flag in the database showing how Chl a was determined. For consistency, we use only Chl a data retrieved from SeaWiFS in the following multilinear and network models.
SeaWiFS photosynthetically available radiation (PAR) and diffuse attenuation coefficient for downwelling irradiance at 490 nm (Kd490) (monthly average, both are L3BIN with spatial resolution of 9.2 km, last access: 1 May 2020) from September 1997 to August 2010 were matched with DMS according to coordinates and sampling date. Mixed layer depth climatologies were obtained from the MIMOC climatology (Schmidtko et al., 2013). Sea ice cover was from a simulation with the ocean component of the Community Earth System Model (CESM) forced with a repeating 30-year cycle (1980–2009) of NCEP reanalysis datasets (Wang et al., 2019). The output was averaged into a monthly climatology and was used as part of the air–sea gas exchange calculations. Nutrient data (nitrate, phosphate, and silicate) from World Ocean Atlas (WOA2013, Garcia et al., 2013) were also included in the multilinear regression and neural network analyses, since they can exert influence on phytoplankton distribution and thus influence DMS production (Wang et al., 2015; Archer et al., 2009). The ancillary data are then matched with DMS data according to sampling location and time of year.
The entire dataset is subjected to another round of quality control following Galí et al. (2015). Specifically, coastal data with salinity lower than 30 and samples with sampling depth greater than 10 m were removed. Additionally, data with extremely low nutrient concentrations (e.g., dissolved inorganic phosphate (DIP) < 0.01 µM, dissolved inorganic nitrate (DIN) < 0.01 µM, SiO4<0.1 µM) or low Chl a concentrations (Chl a < 0.01 mg m−3) were also removed because (a) the low concentrations are below traditional method detection limits and (b) they cause the data distributions to be severely left skewed, which significantly affects the performance of an ANN model.
2.2 Linear regressions
Linear regression models are conducted on three sets of data to diagnose the predictive skill of each ancillary variable. As a first step, we restrict the regression model to the PMEL datasets where both DMS and the predictor variable are simultaneously available. This selection process yields a total of 10 404 pairs for Chl a and DMS, 4061 pairs of total DMSP (DMSPt) and DMS, 69 197 pairs of SST and DMS, and 85 150 pairs of SSS and DMS, respectively. In a second step, we conduct regression models on combined PMEL and NAAMES data. Since almost all NAAMES samples are accompanied by in situ measurements of Chl a, SSS, and SST, the data pairs increased to 17 153 pairs for Chl a and DMS, 75 983 pairs of SSS and DMS, and 91 936 pairs of SST and DMS, respectively. In a third step, to keep Chl a data sources consistent as described previously, we use satellite Chl a; the other unmeasured predictors (i.e., MLD, PAR, DIN, DIP, and silicate (SiO4), SST, and SSS) are filled in using monthly climatology data from the previously cited sources. DMSPt is not included, because there is no observation-based climatological dataset to fill the missing values.
To reduce the dynamic range, we log-transform the DMS, DMSPt, Chl a, MLD, DIP, DIN, SiO4, and SST after conversion to absolute temperature to avoid losing data with temperatures below or equal to 0 ∘C. The corresponding predictors are then standardized to their z score, , where C is predictor's concentration, is the mean of the variables, and σ is the standard deviation of the variables. MATLAB's polyfit function is applied to each pair to fit a first-degree polynomial, i.e., a linear regression.
2.3 Multilinear regression
We begin by applying a stepwise multilinear regression model to the environmental data using MATLAB's stepwiselm function. In a first test, we consider a total of eight potential DMS predictors: PAR, MLD, Chl a, SSS, SST, DIN, DIP, and SiO4. In a second test, we combine the above eight potential parameters with sampling location and time parameters (Eqs. 1–3). The multilinear regression model and the following ANN model require that the predictor fields be available for every DMS data point so we fill missing values in the environmental dataset with climatological data. We eliminate DMS measurements that are under ice cover, leaving us with 82 996 DMS measurements with a complete set of predictors.
The in situ sampling times (months and hours) were converted to periodic functions using sine and cosine functions to address the data continuity issue, such that in a diurnal or seasonal cycle the start (0th hour or January) and the end (24th hour or December) of a cycle share the same properties but are numerically different. The coordinate space notations have a similar issue in the longitudinal direction. The conversions are conducted according to Gade (2010) and Gregor et al. (2017) as follows:
A Bayesian information criterion (BIC) of 0.01 is used as a criterion for accepting or rejecting a predictor, which means that predictors are removed if they induce a BIC increase of more than 0.01.
2.4 Artificial neural network (ANN)
To assess the possibility that a nonlinear model might provide better prediction, we train artificial neural networks (ANNs) using the Keras deep-learning toolbox in Python. DMS concentration along with the eight environmental predictors (PAR, MLD, Chl a, SSS, SST, DIN, DIP, and SiO4) are log-transformed. The predictors' dynamic ranges are then constrained to the  interval using a min–max normalization, i.e., , where Cmin and Cmax are the minimum and maximum values in the data C, respectively.
The dataset is then separated into three sets: training, internal testing, and external validating sets. Data from each of the fourteen 1∘ latitude bands (64–65∘ N, 54–55∘ N, 44–45∘ N, 34–35∘ N, 24–25∘ N, 14–15∘ N, 4–5∘ N, 4–5∘ S, 14–15∘ S, 24–25∘ S, 34–35∘ S, 44–45∘ S, 54–55∘ S, 64–65∘ S) are left out for internal testing (9084 points). Data from each of the fifteen 1∘ latitude bands (69–70∘ N, 59–60∘ N, 49–50∘ N, 39–40∘ N, 29–30∘ N, 19–20∘ N, 9–10∘ N, 1–0∘ S, 9–10∘ S, 19–20∘ S, 29–30∘ S, 39–40∘ S, 49–50∘ S, 59–60∘ S, 69–70∘ S) are left out for external validation (10 870 points). The remaining data (63 042 points) are used to train the neural network. The data are split into the above sets manually rather than automatically. This is because data collected from the same cruise are highly intercorrelated. The common practice of shuffling and randomly splitting the data produces an overfitted model because the validating data can be predicted using near-neighbor values. This kind of apparent skill does not generalize to regions with large data gaps, which we need for constructing a robust climatology. We also manually adjust the hyper-parameters (dropout ratio, hidden layers, number of nodes, etc.) using the data that have been manually divided into training, internal testing, and external validation subsets. After obtaining a satisfactory combination of those hyper-parameters (as discussed below), we fix them and fine-tune the network using all available data.
The network has one input layer with input nodes corresponding to the number of predictors, two dense hidden layers with 128 nodes each, and one output layer with one node corresponding to the predicted logarithm of DMS concentration. To avoid overfitting, we add two dropout layers with a dropout ratio of 25 % after each hidden layer. We also apply a L2 kernel regularizer for each hidden layer with the regulation parameter value set to 0.001. When the network is trained, the mean squared error of the internal validation data is monitored, and the training is stopped when there is no error reduction in 10 epochs. An epoch consists of one forward pass and one backward pass of all the training examples. Only the best model with the lowest validation mean squared error is saved. We tested different network setups – the current setting achieves goodness of fit but avoids overfitting.
2.4.1 Parameter selections
The 15 predictors (8 environmental predictors and 7 time and coordinate signatures) were tested separately. In the first set of tests, we use only time and location parameters. In the second set of tests, we run a series models that examine every possible combination of the eight environmental parameters (a total of 255 combinations). The models are then ranked according to the root mean square error of the validation data.
2.4.2 Monthly climatology
To obtain monthly DMS climatologies, we interpolate the corresponding predictor variables (PAR, MLD, Chl a, SSS, SST, DIN, DIP, and SiO4) onto a 1∘ by 1∘ grid. Coordinates and target months are transformed accordingly. We then apply the top 10 (Sect. 2.4.1) trained networks to obtain DMS monthly concentrations. Monthly results from 10 models are then used to produce the final monthly climatology and to analyze uncertainties.
2.5 Sea-to-air flux
Air–sea gas transfer is estimated using the following bulk formula:
where F is sea-to-air gas exchange flux, Ca and Cw are bulk air and bulk water gas concentrations, and Kw (cm h−1) is the overall gas transfer velocity, expressed in waterside units (Liss, 1974). Kw reflects the combined resistance to gas transfer on both sides of the interface, as follows:
where H is the dimensionless (gas/liquid) Henry law constant, and ka and kw are gas transfer velocities in air and seawater. DMS in the surface ocean is strongly supersaturated with respect to that in the overlying atmosphere (Cw≫Ca), which simplifies the flux Eq. (4) to
For this study we used two parameterizations for Kw. The Goddijn-Murphy et al. (2012) parameterization (hereafter GM12) is based on regressions between satellite-based wind speed observations with shipboard in situ measurements of DMS gas transfer velocities using eddy covariance. The GM12 parameterization for Kw normalized to a Sc number of 660 is
where U10 is a vector of wind speed (m s−1) at 10 m above sea surface. Negative Kw,660 values produced at low wind speeds are set to zero. We also utilized the Nightingale et al. (2000) (hereafter N00), which is based on shipboard 3He∕SF6 dual-tracer experiments. Their parameterization for waterside-only DMS gas transfer velocity at a Schmidt number of 660 (κw,660) is calculated as follows:
where ScDMS is calculated as a function of temperature after Saltzman et al. (1993). A total transfer velocity is obtained from N00 as follows:
where γa is the atmospheric gradient fraction given by (McGillis et al., 2000). Air-side DMS transfer velocity is given as , where MDMS and are the molecular weights of DMS and water, respectively (McGillis et al., 2000).
DMS fluxes were calculated using surface ocean DMS concentrations from the ANN results and a satellite-based wind speed climatology (Table A1 and Fig. A2). Because the N00 parameterization was calibrated using in situ wind speeds and has a nonlinear quadratic dependence on wind speed, the use of monthly mean wind speeds will introduce errors. To reconcile the differences between in situ wind speeds and monthly mean wind speeds, a correction is applied according to Simó and Dachs (2002) by assuming that instantaneous wind speeds follow a Rayleigh distribution. Eq. (8) thus becomes , where , ), and ξ = 2 for the Rayleigh distribution (Livingstone and Imboden, 1993). Ice fraction data are from the CESM simulation monthly climatology. DMS fluxes from ice-covered regions are set to zero, although DMS concentration in or below sea ice is not necessarily zero.
3.1 Linear regressions
The linear regression coefficients and R2 values are summarized in Table 1. For the test using in situ measurements, DMS and DMSPt show the strongest positive correlation with an R2 value of 0.41 (n=4061). Galí et al. (2018) reported a slightly higher R2 value (0.42) with fewer data points (n=3637). It is not surprising to find the strong relationship between total DMSP (DMSPt) and DMS, since DMS derives from the enzymatic cleavage of DMSP (Stefels, 2000; Stefels et al., 2007). Since DMSP is directly produced by phytoplankton and does not undergo sea-to-air gas exchange, it is relatively easy to parameterize in a biogeochemical model (Galí et al., 2015). The strong relationship between DMS and DMSP points toward a potential way to model marine seawater DMS. McParland and Levine (2019) developed a mechanistic model that related intracellular DMSP concentration to environmental stress and coupled the model with the MIT ecosystem model (DARWIN) to estimate global ocean DMSP distribution. Galí et al. (2015) first applied a remote sensing algorithm to obtain a DMSP climatology, from which they predict DMS climatology through an empirical relationship with PAR (Galí et al., 2018).
The second strongest predictor is in situ Chl a (R2=0.21, n=10 404), which is slightly higher than that by Galí et al. (2018), who reported an R2 value of 0.20 (n=8141). The positive correlation between Chl a and DMS is possibly due to the fact that the precursor of DMS, namely DMSP, is biogenic. However, when we test the relationship on satellite-based climatological Chl a, it becomes weaker (PMEL, R2=0.09, n=81 767; PMEL+NAAMES R2=0.09, n=88 516). The weaker relationship can be caused by (1) greater variance in the larger dataset (81 767 vs. 10 404); (2) mismatch between satellite derived Chl a concentrations and analytical Chl a concentrations; and (3) the in situ Chl a samples in PMEL database collected mainly in highly productive regions (Galí et al., 2018), whereas the relationship between Chl a and DMS negatively correlated in oligotrophic oceans over the seasonal cycle (Galí and Simó, 2015).
When tested against climatological data with gaps filled in, PAR has the strongest correlation with DMS (PMEL: R2=0.07, n=82 137; PMEL + NAAMES: R2=0.09, n=88 923), with a positive correlation slope. Climatological MLD is the second strongest predictor (PMEL: R2=0.06, n=81 646; PMEL + NAAMES: R2=0.07, n=88 214) of raw DMS data, with a slope of −0.25 for PMEL and −0.26 for PMEL and NAAMES combined data.
3.2 Multilinear regression
A multilinear regression model that uses a combination of predictors or product of predictors has a higher predictive ability than a linear regression model. For example, a multilinear regression model using eight environmental parameters has an R2 value of 0.28, which is higher than that of any of the linear models. By adding time and location parameters, the R2 value increases to 0.39 (n=82 996, Fig. 1a). The results emphasize the importance of including time and location information in the model. Sampling time and location are useful predictors, especially when the output has strong seasonality such as DMS. Given a location and sampling time, the model roughly predicts the level of DMS concentrations (e.g., high-latitude DMS concentrations are higher in summer than in winter). However, it is apparent that the multilinear regression model significantly underestimates high DMS concentrations. The generally low correlation coefficient hinders the possibility of reliably extrapolating the model to the global ocean.
Figure 1b displays the correlation between DMS observations and ANN predictions. Compared to simple linear and multilinear regression models, ANN captures much more of the observed DMS variance (R2=0.66, n=82 996). Compared to previous extrapolations (Kettle et al., 1999; Lana et al., 2011), the ability of the ANN to build a nonlinear relationship between DMS and environmental predictors allows it to capture more of the variance. The ANN model can also incorporate sampling time and coordinate signals present in the data (see below). As a result, the extrapolation obtained from the ANN considers the relationships with geographical and temporal neighbors.
From traditional linear or multilinear models, one can easily determine which parameter is a strong predictor and how a predictor influences the state variable (e.g., the correlation between DMSP and DMS). An ANN model is much more complex: it adjusts weights of each node that connect inputs and outputs. The relationship between inputs and outputs is therefore much more subtle, and that is why ANN models are generally referred to as a “black box”. In this study, we design experiments that help open this black box and reveal parameters that drive surface ocean DMS distributions.
As shown in Fig. 2, without using any environmental parameters, sampling location and date alone can explain 44 % of the validation data variance (RMSE = 0.65 on a natural logarithm scale). Time of day can be another possible predictor if DMS concentration varies diurnally. However, adding time of day to the model increases RMSE slightly (Fig. 2a). Galí et al. (2013c) studied diel cycle at the Mediterranean Sea and Sargasso Sea. Among their four experiments (three in the Mediterranean Sea and one in the Sargasso Sea) regular diel variation was observed at only one experiment in the Mediterranean Sea in the summer season, with the highest DMS values observed at midnight and the lowest values at midday. In all the other experiments, diel variations for both DMS and DMSPt pools were small. Gross community DMS production during the daytime was 2 to 3 times higher than that in the nighttime, but the high DMS production was compensated for by greater photochemical and microbial consumption (Galí et al., 2013c). The balance between DMS production and consumption appears to dampen DMS diel variation. This may explain why adding time parameters does not improve the ANN model's predictive ability.
Adding environmental parameters can further improve the model performance; however, different parameter combinations show different predictive abilities. Among the top 10 models ranked according to RMSE of validation data
9 models have SST; 8 models have MLD; 5 models have PAR, SSS, and DIP; 4 models have SiO4; and 3 models have Chl a as a predictor, and none of the models have DIN as a predictor. Section 3.7 shows the results of a series of sensitivity tests that demonstrate how each of those parameters influences the DMS distribution.
3.4 Binned data versus raw data
Simó and Dachs (2002) obtained high R2 values between DMS concentration and the ratio of Chl a to MLD (Chl ∕ MLD) when Chl ∕ MLD is greater than or equal to 0.02, as well as between DMS concentration and ln(MLD) when Chl ∕ MLD is less than 0.02. We tried exactly the same model on raw PMEL data with in situ Chl a measurements and climatological MLD and found that both correlations between DMS and Chl ∕ MLD (n=4921, ) and between DMS and ln(MLD) (n=5978, ) are statistically insignificant. To reduce interannual variability, we binned in situ Chl a and DMS into a monthly grid, retested the above model on the binned data, and found that the correlations are still statistically insignificant.
Vallina and Simó (2007) reported an R2 of 0.95 (n=14) between DMS concentration and SRD. We applied the same linear regressions on both raw data and monthly data, and found no significant correlations between DMS and SRD as calculated according to Vallina and Simó (2007):
where SI is shortwave irradiance (W m−2), which is converted from PAR according to Galí and Simó (2015).
Compared to Simó and Dachs (2002) and Vallina and Simó (2007), we used significantly more data points. For example, in this study, there is a total of 10 899 DMS measurements accompanied with simultaneous Chl a measurements versus 2385 data points used in Simó and Dachs (2002), as well as 83 152 (DMS, MLD) pairs in this study versus 26 400 in Vallina and Simó (2007). Another noticeable difference between the current study and previous analyses is that both Simó and Dachs (2002) and Vallina and Simó (2007) binned the data into large longitude and latitude grids. By doing so, the raw data variance is greatly reduced.
Binning data will necessarily result in the loss of information. A lot of information is associated with sampling location and date as shown in Fig. 2a. By binning the data into a monthly grid, the number of data points decreases from 82 996 to only 9018; sampling date features (365) will be averaged to 12 months, and coordinate combinations will be averaged from 87 332×87 332 to , which represents a substantial loss of information. For ANN models, using fewer data points can lead to overfitting. For example, the averaged RMSE on a natural logarithm scale for the 10 best ANN models is 0.608 for the validating dataset and 0.600 for the training dataset when using the unbinned data, whereas the RMSE is 0.655 (validating) and 0.635 (training) for the model constructed using the binned data (See Fig. 2b).
3.5 DMS distributions
Northern Hemisphere and Southern Hemisphere monthly mean DMS concentrations are plotted along with results from previous studies (Simó and Dachs, 2002; Vallina and Simó, 2007; Lana et al., 2011; Galí et al., 2018) (Fig. 3a). Overall, all models show similar seasonal patterns with the highest concentrations in summer and the lowest concentrations in winter. Our predictions are highly consistent with the products derived from satellite data reported by Galí et al. (2018), who used an optimized relationship between DMS, DMSPt, and PAR to obtain DMS climatology from satellite-retrieved PAR and DMSPt fields (Galí et al., 2015). In the Northern Hemisphere, the algorithms by Simó and Dachs (2002) (SD02 hereafter) and by Vallina and Simó (2007) (VS07 hereafter) generate higher concentrations and a smaller seasonal amplitude. From zonal average plots (Fig. 4), it is clear that the elevated monthly means from SD02 are caused by high concentrations in high-latitude oceans, whereas high monthly means of VS07 are caused by high DMS concentrations in low and middle latitude. High DMS concentration in high-latitude summer (SD02) is driven by a shoaling of the MLD caused by high freshwater content (Galí et al., 2018), while high DMS concentrations at low/middle latitude (VS07) are driven by a strong solar radiation dose, which is a joint effect of shallow MLD and strong irradiance.
L11 stands out in the Southern Hemisphere monthly mean plot (Fig. 3b), with the highest mean concentrations in January and December, when DMS concentrations are ∼2 times higher than other model predictions. Galí et al. (2018) identified five shortcomings associated with the direct interpolation method employed by Lana et al. (2011). All shortcomings concern the nature of in situ DMS data, including the right-skewed distribution, lack of spatial and temporal coverage, lack of duplicate measurements, and sampling bias towards DMS-productive conditions. Because of the sparsity and skewed distribution, the interpolation/extrapolation method broadcasts small-scale features to large scales (Tesdal et al., 2016). This is especially true for the month of January and December when the elevated L11 monthly means were mainly driven by a small amount of extremely high DMS measurements (>40 nM) near the Antarctic continent. On the other hand, empirical models including the ANN model used in this study rely on environmental parameter climatologies to obtain the DMS climatology. Extreme conditions are smoothed out in climatological data, e.g., in the DMS database the 99th percentile of in situ Chl a concentration is 12.58 mg m−3, whereas it is only 6.85 mg m−3 in the SeaWiFS climatology. When climatological data are used to generate the DMS distribution, a smaller variance than in situ data is expected.
Figure 5 displays monthly DMS concentration distributions predicted by the ANN. Generally, DMS concentrations in polar regions show strong seasonality. The highest DMS concentrations are in summer when light and temperature are ideal for primary production. For example, in austral summer, the Southern Ocean circumpolar regions, the Scotia Sea, and the Ross Sea display the highest DMS concentration (>10 nM), which gradually decreases and falls below 0.5 nM in the following months when primary production is limited by light or low temperature. In boreal summer, DMS concentration in the Bering Sea and Greenland Sea can exceed 20 nM.
The high DMS concentration during the summertime at high latitudes is believed to accompany blooms of coccolithophores and Phaeocystis, which are strong DMSP producers (Neukermans et al., 2018; Wang et al., 2015). The shoaling mixed layer depth during the summer provides favorable conditions, i.e., stable and warm, with adequate irradiation for coccolithophores and Phaeocystis growth (Galí et al., 2019). Additionally, high DMS concentrations at ice edge zones have also been observed. These high concentrations are due to the release of ice algae that are prolific DMSP producers (Stefels et al., 2012; Webb et al., 2019). As an important cryoprotectant and osmolyte, DMSP helps ice algae to cope with the low-temperature and high-salinity conditions (Thomas and Dieckmann, 2002).
Another interesting region is the Pacific equatorial upwelling region. Large-scale upwelling brings nutrient-rich waters to the surface, which nourish highly productive phytoplankton communities. Overall, the seasonality in the equatorial Pacific is weaker than that in polar regions, but there is still a clear seasonal pattern. In the period from December to April, the tongue with higher DMS concentration (∼3 nM) extends to the west Pacific Ocean reaching the east coast of Australia and the Philippine Sea. The tongue gradually retreats eastward in the following months. From September to November, the tongue is constrained to the eastern Pacific and DMS concentration falls to its lowest values (<2.0 nM). High DMS concentrations in the west Pacific ocean from November to February are also predicted by Lana et al. (2011).
The subtropical gyres show consistently low DMS concentrations and weak seasonal cycles throughout the year. In the Southern Hemisphere gyres, DMS concentrations are highest during austral summer, when the ocean is strongly stratified and local primary production is low. There are hot spots where DMS concentration exceeds 3 nM in December and February. DMS concentrations are generally low (≤1 nM) during austral spring and winter seasons. In the period from April to September, DMS concentrations in the South Atlantic Gyre fall below 0.6 nM. In the Northern Hemisphere gyres, DMS concentrations are high during the boreal summer season. Figure 6 compares monthly mean Chl a concentrations to DMS concentrations in the Northern Hemisphere and Southern Hemisphere gyres. The concentrations are normalized to the range of 0 to 1. It is clear that Chl a and DMS are anticorrelated; DMS concentration peaks in the summer season when Chl a concentration is generally low. This phenomenon has previously been termed as the “summer DMS paradox” (Simó and Pedrós-Alió, 1999). This pattern is more apparent in the Southern Hemisphere gyres, because the terrestrial influence is smaller in the Southern Hemisphere than in the Northern Hemisphere.
3.6 Sea-to-air flux
In this study, we computed monthly sea-to-air DMS fluxes using both the GM12 and N00 gas transfer velocity parameterizations (Figs. 7 and 8). These yield global DMS annual fluxes of 15.89±0.34 Tg S yr−1 (GM12) and 20.12±0.43 Tg S yr−1 (N00), respectively. The uncertainties (±1σ) are calculated according to DMS distributions from the top 10 ANN models based on different parameter combinations. We also calculated sea-to-air DMS fluxes using the N00 parameterization and previous DMS climatologies from Lana et al. (2011) (L11), Simó and Dachs (2002) (SD02), Vallina and Simó (2007) (VS07), and four from Galí et al. (2018) (Gali18). Among those climatologies, VS07 produces the highest annual DMS flux (31.59 Tg S yr−1); the ensemble of Galí et al. (2018) climatologies produce the lowest flux (18.18±0.52 Tg S yr−1) (Table 2). Generally, our fluxes are consistent with previous results when the same flux parameterization, wind speed field, sea surface temperature, and ice coverage are used. The sea-to-air flux based on the GM12 parameterization is ∼24 % lower than that based on N00.
Geographically, in the high-latitude Northern Hemisphere, sea-to-air DMS fluxes are low in boreal winter, even though wind speeds are high. The DMS flux tends to increase in the proceeding months and reaches a maximum in boreal summer, despite the lower wind speeds (Fig. A2). The inverse relationship between wind speed and DMS flux indicates that the high DMS flux is mainly driven by high seawater DMS concentrations. In the Southern Hemisphere, large sea-to-air DMS fluxes at high latitudes in austral summer are driven jointly by high DMS concentrations and high wind speeds (Figs. 7 and A2). The eastern tropical Pacific Ocean displays a year-round intermediate sea-to-air DMS flux. This is mainly driven by the high DMS concentration in this region, since the wind speeds here are generally low (Figs. 7 and A2).
Figure 8 displays integrated monthly global DMS fluxes for both hemispheres and for the global ocean based on GM12 velocity parameterizations. Globally, DMS fluxes are highest in the winter months (December, January, and February) and March, which is mainly driven by high DMS flux in the Southern Hemisphere. There is another peak in the months of July and August because of Northern Hemisphere flux peaks. An interesting feature is that the Northern Hemisphere peak is close to the Southern Hemisphere though and does not reach the peak level in the Southern Hemisphere. This is mainly because of the larger surface area in the Southern Hemisphere. High DMS fluxes in the Southern Hemisphere have profound impact to the Earth's climate because there are less terrestrial and anthropogenic aerosol inputs compared to the Northern Hemisphere.
3.7 Sensitivity tests
Section 3.3 screens key parameter combinations that have the highest prediction skill. To demonstrate how these parameters influence the predicted distribution and sea-to-air flux of DMS, we ran a series of sensitivity tests. In each test, we increase/decrease one environmental parameter at a time. Fig. 9 shows annual mean differences between perturbed models and the control model. These sensitivity tests show regional differences in the sign of the perturbations anomalies. This nonlinear behavior of the ANN model is not possible with a simple linear model.
For the temperature sensitivity test, we uniformly increase SST by 2 ∘C for the whole ocean (Fig. 9a). Compared to the control case, DMS concentrations are lower in most of the low- and middle-latitude oceans and higher in high-latitude oceans, especially in the Southern Ocean, the Bering Sea, and the high-latitude North Atlantic Ocean. In contrast, the linear regression model shows no correlation between SST and DMS. SST alone with date and location parameters has very low prediction ability (ranked 244th over 255 models). When combined with other parameters, SST helps to improve the model performance. For example, the combination of SST and MLD ranks second among all models.
For the mixed layer depth sensitivity test, we decrease MLD by 10 % to mimic the stronger stratification in a warming world (Fig. 9b). DMS concentrations increase in most of the ocean, in line with the linear regression result. In the PAR sensitivity test, we uniformly increase PAR by 10 % with the expectation that light exposure will increase in the future because of MLD shoaling (Fig. 9c). DMS concentrations increase with increased PAR, in agreement with the linear regression result and also with the physiological role of DMS. First, high radiation negatively influences the bacterial population/activity, which decreases DMS consumption (Galí et al., 2013a, b, c; Royer et al., 2016). Second, high radiation promotes DMS production by inducing oxidative stress within algal cells (Toole et al., 2006; Sunda et al., 2002; Royer et al., 2016).
For the salinity sensitivity test, we uniformly decrease surface ocean salinity by 1 psu (practical salinity unit). Similar to the temperature sensitivity result, the changes in DMS concentration show regional variations. DMS concentrations increase in most of the Southern Ocean, the high-latitude North Atlantic Ocean, and the Arctic Ocean, whereas DMS levels decrease in the eastern North Pacific Ocean, the Indian Ocean, and South Atlantic Ocean (Fig. 9d). The linear regression model also shows that there is no significant correlation between DMS and salinity. As in the case for temperature, salinity works synergistically with the other environmental parameters to predict the DMS concentration.
Figure 9e and f show the sensitivity tests for DIP and SiO4, respectively. For these tests, we decrease DIP and SiO4 concentrations by 10 % with the expectation that increasing ocean stratification due to global warming will decrease the nutrient supply from the deep ocean. In certain regions, the two nutrient perturbations have nearly opposite effects. For example, DMS concentrations drop slightly in the western Pacific and Indian Ocean for the DIP perturbation experiment, whereas the concentrations have almost opposite patterns in those regions for the SiO4 perturbation experiment. In the eastern Pacific Ocean, the Southern Ocean, and high-latitude North and South Atlantic oceans, reduced DIP concentration triggers an increase in DMS concentrations, which might be related to nutrient stress, which can increase DMSP production by low DMSP producers (e.g., diatoms) (McParland and Levine, 2019). The increase in DMS concentration for the SiO4 perturbation is potentially due to a regime shift away from diatoms, which are low DMSP producers, to other more prolific DMSP producers.
Figure 9g shows the sensitivity test for Chl a. In the test, we decreased Chl a concentration by 10 % to mimic the decreased primary production caused by ocean stratification and nutrient depletion. Overall, the most apparent changes are in the subtropical gyres, where DMS concentrations are lower than the control run. DMS concentrations increase in some marginal seas and coastal oceans such as the Arabian Sea and eastern coast of Australia. Previous studies of the relationship between DMS and Chl a have produced contradictory results. Strong correlations have been reported in basin-scale studies (e.g., Yang et al., 1999). On the other hand, there are numerous studies that observed no correlation between DMS and Chl a (e.g., Dacey et al., 1998; Kettle et al., 1999; Toole and Siegel, 2004). The inconsistent relationships indicate the complexity of the reduced sulfur cycle.
On a global scale, the increase in temperature does not significantly change sea-to-air flux (15.96 Tg S yr−1 compared to 15.89 Tg S yr−1 for the control run based on GM12) because the elevated DMS concentrations in the high-latitude oceans are compensated for by the reduced concentrations in the low-latitude oceans. Similar to the case for the temperature perturbation, the salinity perturbation has a small effect on the sea-to-air flux of DMS (15.88 compared to 15.89 Tg S yr−1). The overall increases in DMS concentration in the MLD, PAR, and SiO4 perturbation tests lead to increases in DMS sea-to-air flux of 0.56, 0.96, and 0.91 Tg S yr−1, respectively. The Chl a perturbation model is the only one that shows a slight decrease in the sea-to-air flux of DMS (15.59 Tg S yr−1 compared to 15.89 Tg S yr−1).
Of course, the ocean is a very complex system and changes in these environmental parameters will be correlated. For example, the projected temperature increase will lead to a stronger surface ocean stratification that will result in shoaling of MLD and reduced nutrient supplies from the deep ocean, which together will decrease primary production in the ocean. Based on our model results, if these effects work jointly, the DMS sea-to-air flux will increase more than each of the individual perturbations. Assuming that larger DMS sea-to-air fluxes induce greater cloud albedo, then we might expect the changes in DMS to represent a negative climate feedback.
The artificial neural network (ANN) used in this study has some advantages compared to the prior methods used to develop DMS climatologies. Most importantly, the ANN utilizes available measurements to fill regions without DMS observations, using nonlinear relationships trained in more data-rich regions/seasons. By contrast, objective interpolation methods are spatial/temporal averages of sparse data with a weak underlying basis in environmental variability. As a result, the ANN approach captures significantly more of the raw data variance than simple linear/multilinear models. Simple models achieve comparable fits only after heavily binning the DMS observations (e.g., Simó and Dachs, 2002; Galí et al., 2015; Vallina and Simó, 2007; Galí et al., 2018). The ANN is computationally more expensive than the linear/multilinear models but considerably less expensive than prognostic biogeochemical models (e.g., Vogt et al., 2010; Wang and Moore, 2011; Wang et al., 2015). The principal weakness of the ANN approach is that it does not easily provide scientific insight into the relationships between the parameters. We attempted to overcome this weakness by running a series of sensitivity tests to explore how DMS concentration might change in response to global climate warming. We found that the predicted changes in DMS concentration are almost never unidirectional in response to a change in only one environmental parameter. This reveals the underlying interactions between these environmental parameters, which a linear regression model can not achieve.
The ANN approach is a useful tool for developing trace gas climatologies. It may also be useful as a means of assessing the sensitivity of DMS to past/future changes in climate by coupling the ANN to prognostic biogeochemical models. Caution is warranted in the interpretation of such efforts because there is as yet no basis for assessing whether the relationships obtained by training on contemporary measurements apply to the past or will hold in the future. Such relationships could be investigated using paleoceanographic and ice core data (Osman et al., 2019).
The annual sea-to-air DMS flux calculated in this study is slightly (∼23 %) lower than the objective interpolation method of Lana et al. (2011) using the same sea-to-air gas exchange models. DMS concentrations from this study are similar to Lana et al. (2011) where measurements are abundant, so we infer that the difference is likely caused by positive bias in the objective interpolation method for data-sparse regions/seasons.
1 Data from the online database. 2 New data from the North Atlantic Aerosols and Marine Ecosystems Study.
Code for ANN model is available at https://github.com/weileiw/ANN-DMS-code (last access: 15 October 2020, Wang, 2020a).
The data for DMS concentrations and sea-to-air flux are available at https://doi.org/10.5281/zenodo.3833233, (last access: 15 October 2020, Wang, 2020b).
WLW and GS initiated the study and drafted the manuscript. WLW built the model with inputs from FP, ESS, and JKM. ESS and TGB provided new N. Atlantic DMS measurement data. All authors contributed to review the manuscript and to the interpretation of the data presented.
The authors declare that they have no conflict of interest.
We thank the observational DMS community for making their measurements publicly available. We also thank the authors and agencies for providing the ancillary data used in this study (Table A1). We gratefully acknowledge Martí Galí and two anonymous reviewers for their constructive remarks that helped to improve and clarify this paper.
This research has been supported by the DOE Earth System Modeling program (grant no. DE-SC0016539), the Natural Key Research and Development Program of China (grant no. 2017YFC1404403), and the NASA North Atlantic Aerosols and Marine Ecosystems Study (grant no. NNX15AF31G).
This paper was edited by Koji Suzuki and reviewed by Martí Galí and two anonymous referees.
Andreae, M. and Rosenfeld, D.: Aerosol–cloud–precipitation interactions. Part 1. The nature and sources of cloud-active aerosols, Earth.-Sci. Rev., 89, 13–41, 2008. a
Andreae, M. O. and Barnard, W. R.: The marine chemistry of dimethylsulfide, Mar. Chem., 14, 267–279, 1984. a
Archer, S. D., Cummings, D. G., Llewellyn, C. A., and Fishwick, J. R.: Phytoplankton taxa, irradiance and nutrient availability determine the seasonal cycle of DMSP in temperate shelf seas, Mar. Ecol. Prog. Ser., 394, 111–124, 2009. a
Behrenfeld, M. J., Moore, R. H., Hostetler, C. A., Graff, J., Gaube, P., Russell, L. M., Chen, G., Doney, S. C., Giovannoni, S., Liu, H., Proctor, C., Bolaños, L. M., Baetge, N., Davie-Martin, C., Westberry, T. K., Bates, T. S., Bell, T. G., Bidle, K. D., Boss, E. S., Brooks, S. D., Cairns, B., Carlson, C., Halsey, K., Harvey, E. L., Hu, C., Karp-Boss, L., Kleb, M., Menden-Deuer, S., Morison, F., Quinn, P. K., Scarino, A. Jo, Anderson, B., Chowdhary, J., Crosbie, E., Ferrare, R., Hair, J. W., Hu, Y., Janz, S., Redemann, J., Saltzman, E., Shook, M., Siegel, D. A., Wisthaler, A., Martin, M. Y., Ziemba, L.: The North Atlantic Aerosol and Marine Ecosystem Study (NAAMES): Science Motive and Mission Overview, Front. Mar. Sci., 6, 1–25, https://doi.org/10.3389/fmars.2019.00122, 2019. a, b
Bergen, K. J., Johnson, P. A., De Hoop, M. V., and Beroza, G. C.: Machine learning for data-driven discovery in solid Earth geoscience, Science, 363, eaau0323, https://doi.org/10.1126/science.aau0323, 2019. a
Bopp, L., Aumont, O., Belviso, S., and Monfray, P.: Potential impact of climate change on marine dimethyl sulfide emissions, Tellus B, 55, 11–22, 2003. a
Dacey, J. W., Howse, F. A., Michaels, A. F., and Wakeham, S. G.: Temporal variability of dimethylsulfide and dimethylsulfoniopropionate in the Sargasso Sea, Deep-Sea Res. Pt. I, 45, 2085–2104, 1998. a
Derevianko, G. J., Deutsch, C., and Hall, A.: On the relationship between ocean DMS and solar radiation, Geophys. Res. Lett., 36, 2–5, 2009. a, b
Elliott, S.: Dependence of DMS global sea-air flux distribution on transfer velocity and concentration field type, J. Geophys. Res., 114, G02 001, https://doi.org/10.1029/2008JG000710, 2009. a
Frouin, R., McPherson, J., Ueyoshi, K., and Franz, B. A.: A time series of photosynthetically available radiation at the ocean surface from SeaWiFS and MODIS data, in: Proc. Spie., Vol. 8525, p. 852519, International Society for Optics and Photonics, 2012. a
Gade, K.: A Non-singular Horizontal Position Representation, J. Navigation, 63, 395–417, 2010. a
Galí, M. and Simó, R.: A meta-analysis of oceanic DMS and DMSP cycling processes: Disentangling the summer paradox, Global Biogeochem. Cy., 29, 496–515, 2015. a, b
Galí, M., Ruiz-González, C., Lefort, T., Gasol, J. M., Cardelús, C., Romera-Castillo, C., and Simó, R.: Spectral irradiance dependence of sunlight effects on plankton dimethylsulfide production, Limnol. Oceanogr., 58, 489–504, 2013a. a
Galí, M., Simó, R., Pérez, G. L., Ruiz-González, C., Sarmento, H., Royer, S.-J., Fuentes-Lema, A., and Gasol, J. M.: Differential response of planktonic primary, bacterial, and dimethylsulfide production rates to static vs. dynamic light exposure in upper mixed-layer summer sea waters, Biogeosciences, 10, 7983–7998, https://doi.org/10.5194/bg-10-7983-2013, 2013b. a
Galí, M., Simó, R., Vila-Costa, M., Ruiz-González, C., Gasol, J. M., and Matrai, P.: Diel patterns of oceanic dimethylsulfide (DMS) cycling: Microbial and physical drivers, Global Biogeochem. Cy., 27, 620–636, 2013c. a, b, c
Galí, M., Devred, E., Levasseur, M., Royer, S.-J., and Babin, M.: A remote sensing algorithm for planktonic dimethylsulfoniopropionate (DMSP) and an analysis of global patterns, Remote. Sens. Environ., 171, 171–184, 2015. a, b, c, d, e, f, g
Galí, M., Levasseur, M., Devred, E., Simó, R., and Babin, M.: Sea-surface dimethylsulfide (DMS) concentration from satellite data at global and regional scales, Biogeosciences, 15, 3497–3519, https://doi.org/10.5194/bg-15-3497-2018, 2018. a, b, c, d, e, f, g, h, i, j, k, l, m, n, o, p
Galí, M., Devred, E., Babin, M., and Levasseur, M.: Decadal increase in Arctic dimethylsulfide emission, P. Natl. Acad. Sci. USA, 116, 19 311–19 317, 2019. a
Garcia, H. E., Locarnini, R. A., Boyer, T. P., Antonov, J. I., Baranova, O. K., Zweng, M. M., Reagan, J. R., and Johnson, D. R.: World Ocean Atlas 2013, Volume 4: Dissolved Inorganic Nutrients (phosphate, nitrate, silicate), NOAA Atlas NESDIS 76, 25 pp., 2013. a, b, c, d, e, f
Goddijn-Murphy, L., Woolf, D. K., and Marandino, C.: Space-based retrievals of air-sea gas transfer velocities using altimeters: Calibration for dimethyl sulfide, J. Geophys. Res.-Oceans, 117, C08028, https://doi.org/10.1029/2011JC007535, 2012. a, b, c
Gregor, L., Kok, S., and Monteiro, P. M. S.: Empirical methods for the estimation of Southern Ocean CO2: support vector and random forest regression, Biogeosciences, 14, 5551–5569, https://doi.org/10.5194/bg-14-5551-2017, 2017. a
Gypens, N., Borges, A. V., Speeckaert, G., and Lancelot, C.: The dimethylsulfide cycle in the eutrophied Southern North Sea: A model study integrating phytoplankton and bacterial processes, PLoS ONE, 9, e85862, https://doi.org/10.1371/journal.pone.0085862, 2014. a
Humphries, G. R., Deal, C. J., Elliott, S., and Huettmann, F.: Spatial predictions of sea surface dimethylsulfide concentrations in the high arctic, Biogeochemistry, 110, 287–301, 2012. a
Kettle, A. J., Andreae, M. O., Amouroux, D., Andreae, T. W., Bates, T. S., Berresheim, H., Bingemer, H., Boniforti, R., Curran, M. A., DiTullio, G. R., Helas, G., Jones, G. B., Keller, M. D., Kiene, R. P., Leek, C., Levasseur, M., Malin, G., Maspero, M., Matrai, P., McTaggart, A. R., Mihalopoulos, N., Nguyen, B. C., Novo, A., Putaud, J. P., Rapsomanikis, S., Roberts, G., Schebeske, G., Sharma, S., Simó, R., Staubes, R., Turner, S., and Uher, G.: A global database of sea surface dimethylsulfide (DMS) measurements and a procedure to predict sea surface DMS as a function of latitude, longitude, and month, Global Biogeochem. Cy., 13, 399–444, 1999. a, b, c, d, e, f
Kiene, R. P., Linn, L. J., and Bruton, J. A.: New and important roles for DMSP in marine microbial communities, J. Sea Res., 43, 209–224, 2000. a
Lana, A., Bell, T. G., Simó, R., Vallina, S. M., Ballabrera-Poy, J., Kettle, A. J., Dachs, J., Bopp, L., Saltzman, E. S., Stefels, J., Johnson, J. E., and Liss, P. S.: An updated climatology of surface dimethlysulfide concentrations and emission fluxes in the global ocean, Global Biogeochem. Cy., 25, GB1004, 2011. a, b, c, d, e, f, g, h, i, j, k, l
Le Clainche, Y., Vézina, A., Levasseur, M., Cropp, R. A., Gunson, J. R., Vallina, S. M., Vogt, M., Lancelot, C., Allen, J. I., Archer, S. D., et al.: A first appraisal of prognostic ocean DMS models and prospects for their use in climate models, Global Biogeochem. Cy., 24, GB3021, 2010. a
Liss, P. S.: Flux of gases across the air-sea interface, Nature, 247, 181–184, 1974. a
Livingstone, D. M. and Imboden, D. M.: The non-linear influence of wind-speed variability on gas transfer in lakes, Tellus B, 45, 275–295, 1993. a
Longhurst, A. R.: Provinces: The Secondary Compartments, in: Ecological geography of the sea, 2nd edn., Academic Press, San Diego, 2007. a
McGillis, W., Dacey, J., Frew, N., Bock, E., and Nelson, R.: Water-air flux of dimethylsulfide, J. Geophys. Res.-Oceans, 105, 1187–1193, 2000. a, b
McParland, E. L. and Levine, N. M.: The role of differential DMSP production and community composition in predicting variability of global surface DMSP concentrations, Limnol. Oceanogr., 64, 757–773, 2019. a, b
Morel, A., Huot, Y., Gentili, B., Werdell, P. J., Hooker, S. B., and Franz, B. A.: Examining the consistency of products derived from various ocean color sensors in open ocean (Case 1) waters in the perspective of a multi-sensor approach, Remote. Sens. Environ., 111, 69–88, 2007. a
NASA: SeaWinds on QuickSCAT Level 3 surface wind speed for climate model comparison, Ver. 1, PO.DAAC, CA, USA, https://doi.org/10.5067/QSSWS-CMIP1, 2012. a
NASA: Goddard Space Flight Center, Ocean Ecology Laboratory, Ocean Biology Processing Group, Sea-viewing Wide Field-of-view Sensor (SeaWiFS) Ocean Color Data, NASA OB.DAAC, https://doi.org/10.5067/ORBVIEW-2/SEAWIFS_OC.2014.0, 2018. a
Neukermans, G., Oziel, L., and Babin, M.: Increased intrusion of warming Atlantic water leads to rapid expansion of temperate phytoplankton in the Arctic, Glob. Change Biol., 24, 2545–2553, 2018. a
Nightingale, P. D., Malin, G., Law, C. S., Watson, A. J., Liss, P. S., Liddicoat, M. I., Boutin, J., and Upstill-Goddard, R. C.: In situ evaluation of air-sea gas exchange parameterizations using novel conservative and volatile tracers, Global Biogeochem. Cy., 14, 373–387, 2000. a, b, c
Osman, M. B., Das, S. B., Trusel, L. D., Evans, M. J., Fischer, H., Grieman, M. M., Kipfstuhl, S., McConnell, J. R., and Saltzman, E. S.: Industrial-era decline in subarctic Atlantic productivity, Nature, 569, 551, https://doi.org/10.1038/s41586-019-1181-8, 2019. a
Rafter, P. A., Bagnell, A., Marconi, D., and DeVries, T.: Global trends in marine nitrate N isotopes from observations and a neural network-based climatology, Biogeosciences, 16, 2617–2633, https://doi.org/10.5194/bg-16-2617-2019, 2019. a
Roshan, S. and DeVries, T.: Efficient dissolved organic carbon production and export in the oligotrophic ocean, Nat. Commun., 8, 2036, https://doi.org/10.1038/s41467-017-02227-3, 2017. a
Royer, S.-J., Galí, M., Mahajan, A., Ross, O. N., Pérez, G., Saltzman, E. S., and Simó, R.: A high-resolution time-depth view of dimethylsulphide cycling in the surface sea, Sci. Rep.-UK, 6, 32 325, https://doi.org/10.1038/srep32325, 2016. a, b
Saltzman, E., King, D., Holmen, K., and Leck, C.: Experimental determination of the diffusion coefficient of dimethylsulfide in water, J. Geophys. Res.-Oceans, 98, 16 481–16 486, 1993. a
Sathyendranath, S., Stuart, V., Nair, A., Oka, K., Nakane, T., Bouman, H., Forget, M.-H., Maass, H., and Platt, T.: Carbon-to-chlorophyll ratio and growth rate of phytoplankton in the sea, Mar. Ecol. Prog. Ser., 383, 73–84, 2009. a
Schmidtko, S., Johnson, G. C., and Lyman, J. M.: MIMOC: A global monthly isopycnal upper-ocean climatology with mixed layers, J. Geophys. Res.-Oceans, 118, 1658–1672, 2013. a, b
Simó, R.: Production of atmospheric sulfur by oceanic plankton: Biogeochemical, ecological and evolutionary links, Trends Ecol. Evol., 16, 287–294, 2001. a, b
Simó, R. and Dachs, J.: Global ocean emission of dimethylsulfide predicted from biogeophysical data, Global Biogeochem. Cy., 16, 26–1, 2002. a, b, c, d, e, f, g, h, i, j, k, l, m
Simó, R. and Pedrós-Alió, C.: Short-term variability in the open ocean cycle of dimethylsulfide, Global Biogeochem. Cy., 13, 1173–1181, 1999. a, b
Stefels, J.: Physiological aspects of the production and conversion of DMSP in marine algae and higher plants, J. Sea Res., 43, 183–197, 2000. a
Stefels, J., Steinke, M., Turner, S., Malin, G., and Belviso, S.: Environmental constraints on the production and removal of the climatically active gas dimethylsulphide (DMS) and implications for ecosystem modelling, Biogeochemistry, 83, 245–275, 2007. a, b
Stefels, J., Carnat, G., Dacey, J. W., Goossens, T., Elzenga, J. T. M., and Tison, J.-L.: The analysis of dimethylsulfide and dimethylsulfoniopropionate in sea ice: Dry-crushing and melting using stable isotope additions, Mar. Chem., 128, 34–43, 2012. a
Sunda, W. G., Kieber, D., and Kiene, R. P.: An antioxidant function of DMSP and DMS in marine algae, Nature, 418, 317–320, 2002. a
Tesdal, J.-E., Christian, J. R., Monahan, A. H., and von Salzen, K.: Evaluation of diverse approaches for estimating sea-surface DMS concentration and air–sea exchange at global scale, Environ. Chem., 13, 390–412, 2016. a, b
Thomas, D. and Dieckmann, G.: Antarctic sea ice–a habitat for extremophiles, Science, 295, 641–644, 2002. a
Toole, D., Slezak, D., Kiene, R., Kieber, D., and Siegel, D.: Effects of solar radiation on dimethylsulfide cycling in the western Atlantic Ocean, Deep-Sea Res. Pt. I, 53, 136–153, 2006. a
Toole, D. A. and Siegel, D. A.: Light-driven cycling of dimethylsulfide (DMS) in the Sargasso Sea: Closing the loop, Geophys. Res. Lett., 31, https://doi.org/10.1029/2004GL019581, 2004. a, b
Vallina, S. M. and Simó, R.: Strong Relationship Between DMS and the Solar Radiation Dose over, Science, 315, 506–509, 2007. a, b, c, d, e, f, g, h, i, j, k, l, m
Vogt, M., Vallina, S. M., Buitenhuis, E. T., Bopp, L., and Le Quéré, C.: Simulating dimethylsulphide seasonality with the Dynamic Green Ocean Model PlankTOM5, J. Geophys. Res., 115, C06 021, https://doi.org/10.1029/2009JC005529, 2010. a, b
Wang, W. L.: Neural Network regression model to predict DMS monthly climatology, available at: https://github.com/weileiw/ANN-DMS-code, last access: 15 October 2020a. a
Wang, W. L.: DMS monthly climatology predicted using Neural Network regression models, available at: https://doi.org/10.5281/zenodo.3833233, last access: 15 October 2020b. a
Wang, S. and Moore, J. K.: Incorporating Phaeocystis into a Southern Ocean ecosystem model, J. Geophys. Res., 116, C01 019, https://doi.org/10.1029/2009JC005817, 2011. a
Wang, S., Elliott, S., Maltrud, M., and Cameron-Smith, P.: Influence of explicit Phaeocystis parameterizations on the global distribution of marine dimethyl sulfide, J. Geophys. Res.-Biogeo., 120, 2158–2177, 2015. a, b, c, d
Wang, W.-L., Moore, J. K., Martiny, A. C., and Primeau, F. W.: Convergent estimates of marine nitrogen fixation, Nature, 566, 205–211, 2019. a, b
Webb, A. v., van Leeuwe, M., den Os, D., Meredith, M., Venables, H., and Stefels, J.: Extreme spikes in DMS flux double estimates of biogenic sulfur export from the Antarctic coastal zone to the atmosphere, Sci. Rep.-UK, 9, 1–11, 2019. a
Yang, G. P., Liu, X. T., Li, L., and Zhang, Z. B.: Biogeochemistry of dimethylsulfide in the South China Sea, J. Mar. Res., 57, 189–211, 1999. a, b