Macroalgal metabolism and lateral carbon flows can create significant carbon sinks
Macroalgal beds have drawn attention as one of the vegetated coastal ecosystems that act as atmospheric CO2 sinks. Although macroalgal metabolism as well as inorganic and organic carbon flows are important pathways for CO2 uptake by macroalgal beds, the relationships between macroalgal metabolism and associated carbon flows are still poorly understood. In the present study, we investigated carbon flows, including air–water CO2 exchange and budgets of dissolved inorganic carbon, total alkalinity, and dissolved organic carbon (DOC), in a temperate macroalgal bed during the productive months of the year. To assess the key mechanisms responsible for atmospheric CO2 uptake by the macroalgal bed, we estimated macroalgal metabolism and lateral carbon flows (i.e., carbon exchanges between the macroalgal bed and the offshore area) by using field measurements of carbon species, a field-bag method, a degradation experiment, and mass-balance modeling in a temperate Sargassum bed over a diurnal cycle. Our results showed that macroalgal metabolism and lateral carbon flows driven by water exchange affected air–water CO2 exchange in the macroalgal bed and the surrounding waters. Macroalgal metabolism caused overlying waters to contain low concentrations of CO2 and high concentrations of DOC that were efficiently exported offshore from the macroalgal bed. These results indicate that the exported water can potentially lower CO2 concentrations in the offshore surface water and enhance atmospheric CO2 uptake. Furthermore, the Sargassum bed exported 6 %–35 % of the macroalgal net community production (NCP; 302–1378 mmol C m−2 d−1) as DOC to the offshore area. The results of degradation experiments showed that 56 %–78 % of macroalgal DOC was refractory DOC (RDOC) that persisted for 150 d; thus, the Sargassum bed exported 5 %–20 % of the macroalgal NCP as RDOC. Our findings suggest that macroalgal beds in habitats associated with high water exchange rates can create significant CO2 sinks around them and export a substantial amount of DOC to offshore areas.
Vegetated coastal ecosystems provide a variety of ecosystem functions that support diverse biological communities and biogeochemical processes. Recent recognition of the carbon sequestration function of these ecosystems has led to the development of blue carbon strategies for mitigating the adverse effects of global climate change via conservation and restoration of these ecosystems (Nellemann et al., 2009; Duarte et al., 2013; Macreadie et al., 2019).
Carbon flows that sequester atmospheric CO2 in marine ecosystems over timescales of at least several decades are crucial for the mitigation of climate change (McLeod et al., 2011; Macreadie et al., 2019). Organic carbon burial in sediments is one of the most important pathways for sequestering carbon for a long time (Nellemann et al., 2009; Miyajima et al., 2019). Evaluation of the carbon sequestration function of vegetated coastal ecosystems has thus far been focused on salt marshes, seagrasses, and mangroves, which develop their own organic-rich sediments (Macreadie et al., 2019). In contrast, beds of macroalgae have been assumed to have limited capacity to sequester carbon because they generally settle on hard strata such as rocks and artificial structures (Krause-Jensen et al., 2018). Organic matter produced by macroalgae shows variable lability, but it is generally more labile than that produced by vascular plants (Trevathan-Tackett et al., 2015) and hence is more efficiently utilized by consumers and decomposers (Duarte, 1995). However, macroalgal beds are estimated to be the most extensive vegetated coastal habitats (3.5×106 km2) in the global ocean, and their global net primary production (1521 Tg C yr−1) is larger than that of other vegetated coastal habitats (Krause-Jensen and Duarte, 2016; Duarte, 2017; Raven, 2018). Macroalgal beds therefore have the potential to regulate carbon dynamics in coastal ecosystems.
Other processes in addition to organic carbon burial in on-site sediments must exist for macroalgae to contribute to atmospheric CO2 sequestration. Recent studies have proposed that a large fraction of macroalgal production is exported to other vegetated coastal ecosystems, shelves, and the deep sea, where organic carbon derived from macroalgae can be stored in sediments and the water column for a long time (Krause-Jensen and Duarte, 2016; Krause-Jensen et al., 2018; Queirós et al., 2019).
The export and persistence of macroalgal dissolved organic carbon (DOC) have been proposed to be principal processes of macroalgal carbon sequestration, but more empirical support is needed to quantify this carbon flow. Macroalgal beds export about 43 % of their production as DOC and particulate organic carbon (POC) (Krause-Jensen and Duarte, 2016). A first-order estimate has suggested that 33 % of the flux of DOC derived from macroalgae is exported to depths below the mixed layer, where it contributes to carbon sequestration (Bauer and Druffel, 1998; Krause-Jensen and Duarte, 2016). Because the proportion of exported carbon that persists for a long time is estimated to be higher in DOC (33 %) than in POC (15 %) (Krause-Jensen and Duarte, 2016), DOC production, export, and degradation are believed to be significant processes for carbon sequestration. Although the production of refractory DOC by macroalgae is one of the important factors that impact carbon sequestration, there are few relevant data (e.g., Wada et al., 2008; Wada and Hama, 2013). The long residence time of refractory DOC in the water column increases the probability that it reaches depths below the mixed layer.
Even though macroalgal beds perform a significant function by assimilating organic carbon, the chemical kinetics of the carbonate system in the water column could cause them to be net CO2 emitters via air–water CO2 exchange. The dissolved constituents of the carbonate system must therefore be assessed to quantify the effect of community metabolism on air–water CO2 exchange (Macreadie et al., 2019; Tokoro et al., 2019). The high rates of macroalgal photosynthesis and respiration change dissolved inorganic carbon (DIC) concentrations. Calcification and dissolution of associated organisms modify the total alkalinity (TAlk) and DIC. Physical parameters and the balance of the carbonate system decide the magnitude of the air–water CO2 exchange (Tokoro et al., 2019). Indeed, some previous studies have shown that macroalgal beds act as sinks for atmospheric CO2 (Delille et al., 2009; Ikawa and Oechel, 2015; Koweek et al., 2017) and contribute substantially to global carbon fluxes (Smith, 1981; Krause-Jensen and Duarte, 2016). Macroalgal metabolism regulates diurnal and temporal variations in carbonate chemistry and affects calcification by calcifiers in macroalgal beds (Middelboe and Hansen, 2007; Krause-Jensen et al., 2015, 2016; Duarte and Krause-Jensen, 2018; Wahl et al., 2018). However, there is limited field evidence for how the effects of macroalgal metabolism on the carbonate system extend to adjacent water bodies.
Despite the importance of dissolved carbon flows as CO2 sequestration pathways, little attention has been paid to assessing the related carbon budgets in macroalgal beds. In this study, we assessed carbon flows, including air–water CO2 exchange and changes of DIC, TAlk, and DOC, in a temperate macroalgal bed during productive periods (winter). To quantify macroalgal metabolism and dissolved carbon flows, we used a field-bag method, a degradation experiment, and mass-balance modeling. In the present study, we focused on Sargassum beds because they are one of the dominant macroalgal habitats in both temperate and tropical regions (e.g., Fulton et al., 2019; Yoshida et al., 2019). Our goals were to quantify the contribution of macroalgal beds to atmospheric CO2 uptake and to investigate the responsible mechanisms on a daily timescale.
2.1 Study site and sample collection
This study was conducted in the coastal waters of Heigun Island (33∘46′1.7′′ N, 132∘15′24.3′′ E) in the western Seto Inland Sea of Japan (Fig. 1). The macroalgal bed at the study site is dominated by Sargassum algae (Figs. S1 and S2 in the Supplement). The surface area of the macroalgal bed is 1.44 ha, and the macroalgal habitat is located at depths shallower than 5 m (mean depth – 2.0 m). There is no significant freshwater input from the island. The study site is characterized by a relatively high tidal amplitude (<4 m), and it is adjacent to a deep strait (∼60 m).
Field surveys were conducted in February and March of 2019 in the macroalgal bed and the adjacent water bodies to take into account the temporal variations in biotic and abiotic conditions. Winter, including the months of February and March, is the most productive period of Sargassum algae around this study site (Yoshida et al., 2001). Surface water samples for analyses of DIC, TAlk, and DOC were collected from a research vessel three times (10:00, 13:00, and 16:00 JST – Japan standard time) during the daytime (approximately from 7:00 to 17:00 JST) during both surveys at five stations (H1–H5; Fig. 1). Four stations (H1–H4) inside the macroalgal bed were chosen at equal intervals between the ends of the bed to assess average conditions. Station H5 was established at an offshore site. Samples for DIC and TAlk were dispensed into 250 mL Schott Duran bottles and preserved with mercuric chloride (200 µL per bottle) to prevent DIC changes due to biological activity. Water samples for DOC analysis were filtered through 0.2 µm polytetrafluoroethylene filters (DISMIC–25HP; Advantec, Durham, NC, USA) into precombusted (450 ∘C for 2 h) 50 mL glass vials and frozen at −20 ∘C until analysis. At each station, the salinity, temperature, and chlorophyll fluorescence of the surface water were recorded with a RINKO-Profiler (ASTD102, JFE Advantech, Nishinomiya, Japan).
Field-bag experiments (e.g., Towle and Pearse, 1973; Wada et al., 2007) were conducted to quantify the changes of DIC, TAlk, and DOC by macroalgae during 1 d in both February and March of 2019. We selected Sargassum horneri as the subject species because sufficient amounts of S. horneri were present in a zone suitable for the experiments. The entire thallus of an individual S. horneri was covered with a plastic bag containing ambient seawater collected in the macroalgal bed. The open end of the bag was tied at the algal stipe by scuba divers. Triplicate transparent and dark bags were set up to measure the changes of dissolved constituents due to macroalgal metabolism (Fig. S3). To assess the effect of phytoplankton, a set of transparent and dark bags were filled with ambient seawater that was collected in the macroalgal bed but contained no macroalgae. These bags served as control bags. Water samples from the bags were collected just after the start of the experiment and about 4 h later through a Tygon® tube by using a hand-held vacuum pump. The collected water samples were preserved with mercuric chloride for the carbonate chemistry analysis and filtered through the 0.2 µm filters for the DOC analysis (vide supra). After the experiments, the volume of seawater and the wet weight of the macroalgae in each bag were measured. At the beginning and end of the experiments, the salinity, temperature, and chlorophyll fluorescence of the surface water were recorded with a RINKO-Profiler (ASTD102, JFE Advantech). Photosynthetic photon flux was measured with a photon flux sensor (DEFI-L, JFE Advantech) during the experiments.
The assessment of the biomass and species composition of the macroalgal bed that we studied was conducted in March 2019. Two 120 m transect lines were set from the shoreline to the edge of the macroalgal bed to document the biomass, coverage, and species composition of the macroalgae (Fig. 1). To assess the coverage and species composition, 1 m × 1 m quadrats were located at 10 m intervals along each transect. Scuba divers quantified the apparent vegetation coverage and species composition in each quadrat. Five quadrats (0.5 m × 0.5 m) were randomly located in the area dominated by Sargassum algae along each transect to quantify the wet weight biomass (g WW – grams wet weight) of the macroalgae. Scuba divers collected all macroalgae in each quadrat. The wet weight of the Sargassum algae and the other macroalgae were then measured immediately.
2.2 Degradation experiment
To quantify the degradation rates of macroalgal DOC due to microbial activity and to estimate the refractory fraction of that DOC, DOC samples for degradation experiments were obtained after the field-bag experiments. Water samples were collected from each transparent bag of macroalgae and control. The samples were filtered through precombusted (450 ∘C for 2 h) glass-fiber filters (0.7 µm pore size; GF/F, Whatman, Maidstone, Kent, UK) under reduced pressure. We assumed that GF/F filters would allow the passage of a significant fraction of free-living bacteria into the experimental samples (e.g., Wada et al., 2008; Bauer and Bianchi, 2011; Kubo et al., 2015).
The 40 mL filtrates were transferred into precombusted (450 ∘C for 2 h) 100 mL glass vials sealed with rubber and aluminum caps. The 60 mL headspace in each glass bottle contained about 540 µmol oxygen, which was sufficient to support the aerobic microbial degradation of DOC (∼220 µmol) in each bottle if 1 mol of oxygen was consumed by the mineralization of 1 mol of DOC into CO2. The degradation experiments were conducted based on a total of six incubations (0, 3, 10, 30, 90, and 150 d) per field survey. Triplicate bottles were used for each incubation. The experimental samples were stored at room temperature (22 ∘C) in total darkness until analysis. In the present study, we used room temperature for both samples to evaluate the quality of the organic matter. After incubation, the samples were filtered through 0.2 µm polytetrafluoroethylene filters (DISMIC–25HP; Advantec) into precombusted (450 ∘C for 2 h) 100 mL glass vials and frozen at −20 ∘C until analysis.
In this study, the concentration of refractory DOC (RDOC) was defined as the concentration of DOC remaining after 150 d, and the concentration of DOC derived from macroalgae (DOCM) was equated to the difference between the DOC concentration in the macroalgae bag and the DOC concentration in the control bag (DOCC). Degradation rates (k) were calculated by a first-order exponential decay model as follows:
where DOCM(t) is the amount of DOCM remaining at time t (d), and k is the degradation rate (d−1).
2.3 Sample analyses
The DIC concentration and TAlk were determined with a batch-sample analyzer (ATT-05 and ATT-15; Kimoto Electric, Osaka, Japan) according to Tokoro et al. (2014). The analytical precision of the system, based on the standard deviation of multiple reference replicates, was normally within ±2 µmol L−1 for DIC and TAlk.
DOC concentrations were measured at least in triplicate with a total organic carbon analyzer (TOC-L; Shimadzu, Kyoto, Japan) as non-purgeable organic carbon according to Ogawa et al. (1999). Potassium hydrogen phthalate (Wako Pure Industries, Osaka, Japan) adjusted to three concentrations (83, 166, and 332 µM) was used as a standard for the measurement. The coefficient of variation of the analyses was less than 2 %.
2.4 Metabolic parameters
Net community production (NCP), gross community production (GCP), community respiration (R), community calcification (CC), and net DOC release (NDR) were determined from the changes in DIC, TAlk, and DOC of the field-bag experiments. These metabolic parameters were determined for both control and macroalgae as follows:
In both the control and macroalgal field-bag experiments, ΔDIC, ΔTAlk, and ΔDOC were equated to the final concentrations minus the initial concentrations. The subscripts L and D indicate transparent (i.e., light) and dark bags, respectively. The variables V, B, and T are the volume of seawater (L), the wet weight of the macroalgae (g WW), and the incubation time (h) in each bag, respectively. The CC and NDR rates were calculated for the daytime and night-time separately by using the data from the light and dark experiments, respectively. The metabolic parameters were converted to daily areal rates (mmol C m−2 d−1) by using the mean macroalgal biomass, the mean water depth, the lengths of the photoperiods, and the results of both daytime and night-time experiments. The photoperiod was defined as the time interval between sunrise and sunset; photoperiods were obtained from Automated Meteorological Data Acquisition System (AMeDAS) data provided by the Japan Meteorological Agency (available at https://www.jma.go.jp, last access: 24 March 2020).
2.5 Air–water CO2 flux
The air–water CO2 flux (FCO2) was determined by using the bulk formula method. The equation for the method is as follows:
where fCO2 is fugacity. The gas transfer velocity (K) was determined from empirical relationships between K and the wind speed above the surface of the water (e.g., Wanninkhof, 1992; McGillis et al., 2001). S is the CO2 solubility in the water. A positive FCO2 value indicates CO2 uptake from the air to the water. Here we used the following empirical equation to estimate K (Wanninkhof, 1992):
where U10 is the wind speed at a height of 10 m above the water surface. We determined U10 by assuming that there was a logarithmic relationship between wind speed, height, and the roughness of the water surface (Kondo, 2000). Wind speed was obtained from AMeDAS data provided by the Japan Meteorological Agency and was measured about 10 km away at Agenosho (altitude: 6.5 m) (available at https://www.jma.go.jp). The Schmidt number (Sc) was determined from the water temperature and salinity of the water surface.
The solubility (S) of CO2 is a function of water temperature and salinity (Weiss, 1974). fCO2 water and fCO2 air are the fugacities of CO2 in water and air, respectively. The values of fCO2 water were estimated with the CO2SYS program (Lewis and Wallace, 1998) and the TAlk and DIC of the water samples (Zeebe and Wolf-Gladrow, 2001). The average salinity and water temperature were used to calculate fCO2 water in each survey. We used the averaged fCO2 air (410 µatm) measured with a CO2 analyzer (CO2-09; Kimoto Electric, Osaka, Japan).
2.6 Mass-balance modeling
We simulated the diurnal changes and budgets of the carbonate system and DOC in the macroalgal bed by using mass-balance models (Fig. 2). The mass-balance models of the macroalgal bed simulated a hypothetical average macroalgal bed covering an area of 1 m2. The average depth of the hypothetical macroalgal bed was the same as that of the macroalgal bed at the study site (2.0 m), and the tide was simulated by changing the water height in synchrony with the observed tide. We used the average biomass of Sargassum algae obtained from the field survey in the mass-balance models. This modeling was conducted solely for the macroalgal bed, and the observed values of the offshore site (H5) were used as the boundary conditions for carbon inflowing into the macroalgal bed.
Time course changes in the concentrations of DIC, TAlk, and DOC (µmol L−1) in the macroalgal bed were calculated at hourly time intervals (Fig. 2). The duration of the simulation was 24 h, beginning at sunrise of the survey day. Each concentration at time step (t) was calculated from the concentration at time step (t−1) as follows:
Metabolic parameters (GCP, R, CC, and NDR) were determined from changes in DIC, TAlk, and DOC measured in the field-bag experiments (Fig. 2 and Table S1 in the Supplement). These metabolic parameters were calculated as the sum of the contributions from both macroalgae and phytoplankton. The parameters DICO, TAlkO, and DOCO in Eqs. (14)–(16) are the mean values of DIC, TAlk, and DOC, respectively, at the offshore station (H5), and the initial values in the simulation were equated to those values. Namely, DIC(0), TAlk(0), and DOC(0) were equated to DICO, TAlkO, and DOCO, respectively. We assumed that there was no biogeochemical exchange between the bottom substrate and water. In the simulation, we assumed that the metabolic parameters (GCP, R, CC, and NDR) of S. horneri were applied to the entire macroalgal bed and used different metabolic parameters for day and night. EX (1), the hourly water exchange rate, was defined as follows:
EXtide indicates the water exchange rate due to tidal change. EXtide was estimated from the changes of water height (H) and was positive during the flood tide and zero during the ebb tide. EXr was defined as the residual exchange rate due to factors other than tidal exchange (e.g., wind-driven water exchange and coastal currents). The value of EXr was chosen so as to minimize the root-mean-square error (RMSE) of the modeled values versus the observed values. RMSEs were calculated for the z scores of DIC, TAlk, DOC, and fCO2, which were equated to the differences between the modeled values and the means of the observed values divided by the standard deviations of the observed values. The value of EXr that minimized the averaged RMSEs for these four parameters was determined for each survey. This model fitting was performed using the daytime data. The estimated EXr was applied throughout the diurnal cycle on the assumption that EXr was comparable during the day and night. We ran two different model scenarios, one with and the other without water exchange (i.e., EX).
The budgets of DIC, TAlk, and DOC were calculated as the net gain or loss of each constituent due to water exchange. The changes in fCO2, which were estimated by using chemical equilibrium relationships and the TAlk and DIC of the water samples (Lewis and Wallace, 1998; Zeebe and Wolf-Gladrow, 2001), were used to calculate FCO2. The average salinity and water temperature were used to calculate fCO2 in each survey.
2.7 Statistical analyses
Statistical analyses were performed by using R statistical packages (R Core Team, 2019). We used Welch's two-sample t test to determine whether there were differences in salinity, DIC, TAlk, fCO2, and DOC between the macroalgal bed and the offshore site and to detect the differences between the initial and final concentrations of DOC during degradation experiments.
3.1 Carbonate system and DOC in the macroalgal bed
There were no differences in salinity and TAlk between the macroalgal bed (n=12) and the offshore site (n=3) in either February or March (Welch's two-sample t test, p>0.05; Fig. 3 and Table S2). The DIC concentration was significantly lower in the macroalgal bed (1964±22 µmol L−1) than at the offshore site (1991±1 µmol L−1) in February (p=0.002) (Fig. 3 and Table S2). In March, the variation in the DIC concentration was large (1962±43 µmol L−1) in the macroalgal bed but was also significantly lower than at the offshore site (1992±1 µmol L−1; p=0.033). The fCO2 values were significantly lower in the macroalgal bed than at the offshore site in both February (p=0.001) and March (p=0.025; Fig. 3 and Table S2). The fCO2 values in the macroalgal bed (February – 265±31 µatm; March – 272±49 µatm) and the offshore site (February – 305±3 µatm; March – 309±1 µatm) were lower than fCO2 air (410 µatm). On average, the DOC concentrations were higher in the macroalgal bed than at the offshore site, but the difference between them was significant only in March (p=0.010; Fig. 3 and Table S2). fCO2 was strongly correlated with DIC in both February and March (Fig. 4). The homogeneous buffer factors (β), which were equated to the slopes of log–log plots of fCO2 versus DIC, were 10.81 and 9.36 in February and March, respectively.
Community carbon metabolism was calculated from the field-bag experiments (Tables 1 and S1). The NCP of macroalgae was about 4 times higher in March (1378 mmol C m−2 d−1) than in February (302 mmol C m−2 d−1) (Table 1) and was considerably higher than that of phytoplankton (∼22 mmol C m−2 d−1). The net community calcification (NCC) of macroalgae was positive during both months (11–21 mmol C m−2 d−1), but the average carbon fluxes due to NCC were 1–2 orders of magnitude lower than those associated with NCP. The net DOC release rates of macroalgae were 107 and 88 mmol C m−2 d−1 in February and March, respectively. These values were equivalent to about 35 % and 6 % of the NCP in February and March, respectively.
3.2 Biomass and species composition of macroalgae
The macroalgal bed was dominated by Sargassum algae (Figs. 5, S1, and S2). The biomass of Sargassum algae (mean: 4693 g WW m−2) was higher than that of the other macroalgae (264 g WW m−2) (Fig. 5). The coverage of Sargassum algae (∼80 %) was also larger than that of the other macroalgae (∼51 %).
3.3 Degradation of DOC
DOC concentrations collected from macroalgae bags decreased with time in both experiments (Welch's two-sample t test, p<0.05; Fig. 6). In contrast, the stability of DOC concentrations collected from control bags during the experiments (p>0.05) suggested that DOCM gradually decreased with time. Refractory DOCM (RDOCM) concentrations were 56±4 % and 78±27 % of initial DOCM concentrations in February and March, respectively (Fig. 6c). The degradation rate (k) for 150 d incubations was higher in February (0.0044 d−1) than in March (0.0021 d−1).
3.4 Carbon budgets estimated using mass-balance models
The mass-balance models simulated the temporal changes of carbonate chemistry and DOC concentrations for the two model scenarios – that is, with and without considering water exchange (Fig. 3). The RMSEs of the z scores of the best-fitting models considering water exchange (mean: February – 0.56; March – 0.91) were lower than those assuming that water exchange was zero (mean: February – 3.77; March – 3.10; Table 2). The fitted model that took into consideration EX improved the RMSEs of the z scores of all parameters in February. In March, the RMSEs of the z scores of DIC and fCO2 were improved by the model fitting, but those of DOC and TAlk showed little or no improvement (Table 2). The estimated EXr values were 39 % and 42 % in February and March, respectively (Table 3). The EXr rates were the main components of the hourly water exchange rates (the sums of EXtide and EXr), which were estimated to be 39 %–52 % and 42 %–68 % in February and March, respectively (Fig. 3 and Table 3).
DIC concentrations were decreased in the daytime by primary production (Fig. 3a, f). TAlk values in the macroalgal bed were stable and very similar to the TAlk values of the offshore seawater (Fig. 3b, g). The fCO2 decreased during the daytime because of the concurrent decrease in the DIC concentration (Fig. 3c, h). DOC concentrations in the macroalgal bed exceeded those at the offshore site during the daytime (Fig. 3d, i).
DOC was exported offshore from the macroalgal bed (Fig. 7). The areal effluxes of DOC (February – 125 mmol C m−2 d−1; March – 96 mmol C m−2 d−1) were similar to the NDRs. The export fluxes of RDOCM were estimated to be 59 and 67 mmol C m−2 d−1 in February and March, respectively (Fig. 7). DIC budgets driven by water exchange indicated a net input of DIC from offshore to the macroalgal bed (Fig. 7 and Table 3). The areal influxes of DIC were 323 and 1386 mmol C m−2 d−1 in February and March, respectively. These fluxes were almost equivalent to the sum of NCP, NCC, and FCO2 in the macroalgal bed (Fig. 7). The FCO2 values showed that both the macroalgal bed and the offshore site took up atmospheric CO2 during these study periods. FCO2 values were higher in the macroalgal bed than offshore during both periods (Fig. 7 and Table 3).
4.1 Refractory DOC release by macroalgae
Our results showed that the Sargassum bed released a large amount of DOC (Fig. 7). Most of the released DOC was exported out of the macroalgal bed via water exchange during the day. The DOC release rates of S. horneri (18.7–22.8 µmol C g WW−1 d−1; Table S1) were within the range of those reported for Ecklonia kelp (1.5–72.5 µmol C g WW−1 d−1; Wada et al., 2007), which were calculated by assuming that water content was 85 % of wet weight (Watanabe et al., unpublished data). The fact that Wada et al. (2007) collected data over an entire year, whereas our data were collected during only the most productive 2 months of the year, accounts for the difference in the variations in DOC release rates. Previous studies have found that a substantial portion of production is released as DOC by kelps (18 %–62 %; Abdullah and Fredriksen, 2004; Wada et al., 2007). Our results showed that Sargassum algae sometimes release a similar percentage of production as DOC (February – 35 %; March – 6 %), and the percentages were very different between the 2 months, despite the similarity of the DOC release rates (Fig. 7). DOC release rates by kelps have been shown to be correlated with irradiance, but irradiance explained only 13 % of the variation in the DOC release rates (Reed et al., 2015). Time lags between light-stimulated carbon assimilation and DOC release may explain some of the variation between irradiance and DOC release. High-frequency time-series measurements may help to explain the daily variations in macroalgal carbon metabolism. In this study, the reproducibility of the DOC mass-balance model (i.e., the improvement of RMSEs) differed between the February and March data sets (Fig. 3 and Table 2). Temporal and interspecific variations in DOC release rates may have caused this difference.
Refractory organic carbon acts as a carbon reservoir in seawater (Hansell and Carlson, 2014) and is considered to be one of the important contributors to carbon sequestration by coastal macrophytes (Maher and Eyre, 2010; Watanabe and Kuwae, 2015; Krause-Jensen and Duarte, 2016; Duarte and Krause-Jensen, 2017). Our results show that the Sargassum bed exported 5 %–20 % of the macroalgal NCP as RDOC that persisted for 150 d (Fig. 7). The fact that the degradation rates of macroalgal DOC are lower than those of DOC released by phytoplankton (k values, >0.025 d−1; Hama et al., 2004; Kirchman et al., 1991) implies that macroalgal DOC is more biologically recalcitrant than DOC produced by phytoplankton (Wada et al., 2008). Previous studies have suggested that macroalgae produce phenolic compounds such as phlorotannin that are biologically recalcitrant (Swanson and Druehl, 2002; Wada and Hama, 2013; Powers et al., 2019). A thermogravimetric approach has also shown that macroalgal thalli contain refractory compounds (Trevathan-Tackett et al., 2015), some of which are released as the plant grows. These findings indicate that macroalgae release chemically recalcitrant DOC for decomposers.
Wada et al. (2008) have estimated the turnover times of the DOC released by Ecklonia kelp, the reciprocals of the degradation rates (k), to be 24–172 d (i.e., k values of 0.0058–0.0407 d−1) during 30 d incubations. In the present study, the turnover times of DOC released by S. horneri were calculated to be 111–238 d (i.e., k values for 30 d incubations of 0.0042–0.0090 d−1), longer than the turnover times of Ecklonia kelp. These findings indicate that the recalcitrance of macroalgal DOC is variable and depends on the species and environmental conditions. The production of recalcitrant macroalgae compounds such as phlorotannins varies among seasons, growth phases, and species (Steinberg, 1989; Kamiya et al., 2010), and these variations may regulate seasonal and interspecific variations in the biological recalcitrance of macroalgal DOC. Furthermore, degradation rates for 150 d incubations (0.0021–0.0044 d−1; Fig. 6) were slower than those for first 30 d incubations, indicating that relatively short-duration degradation experiments may underestimate the long-term persistence of OC (e.g., Trevathan-Tackett et al., 2020).
The microbial degradation of DOC is also affected by temperature, and high temperature stimulates DOC degradation (e.g., Chen and Wangersky, 1996; Lønborg and Álvarez-Salgado, 2012). In this study, the microbial degradation rates of DOC were potentially overestimated compared to in situ conditions because the incubation temperature for the degradation experiments (22 ∘C) was higher than the in situ temperature (∼13 ∘C; Table 1). The difference in the initial DOCM concentrations in the macroalgae bags between February and March may have been caused by the differences in the biomass of macroalgae and volume of water in the experimental bags (Fig. 6a, b). Variations in DOC concentrations may affect degradation rates via resource limitation of microbial activity (e.g., Arrieta et al., 2015). Understanding of the fate of macroalgal DOC would be enhanced by the assessment of the physical and biochemical factors that regulate microbial degradation of DOC. The rates of DOC degradation processes, which were not measured in this study (e.g., photochemical degradation), might also be important in driving macroalgal DOC degradation (Wada et al., 2015).
Ogawa et al. (2001) have shown that marine bacteria take up labile organic matter (OM) such as glucose and convert it into refractory OM. Some of the macroalgal DOC may be converted to refractory OC by microbes and persist in water for a long time. Carbon flows through the microbial loop should be assessed as one of the fates of OM derived from macroalgal beds.
4.2 CO2 uptake and DIC budgets in the macroalgal bed
Atmospheric CO2 uptake was affected by community metabolism and water exchange, which regulated the carbon budget in the Sargassum algae-dominated macroalgal bed. Positive NCP values showed that the macroalgal bed acted as an autotrophic system during the study periods. Macroalgal DIC uptake (i.e., NCP) accounted for > 97 % of total NCP in this system (Table 1); the rest was attributable to planktonic NCP. Biological uptake of DIC promoted atmospheric CO2 uptake by contributing to the decrease in DIC concentrations and fCO2 during the day inside the macroalgal bed (Figs. 3 and 7).
Previous studies have shown that macroalgal primary production reduces DIC and CO2 concentrations. For example, DIC uptake by kelp reduces fCO2 and thereby contributes to the uptake of atmospheric CO2 inside kelp beds (Delille et al., 2000, 2009; Koweek et al., 2017; Pfister et al., 2019). The aquaculture of macroalgal species such as the kelp Laminaria japonica and the red algae Gracilaria lemaneiformis has also been shown to result in annual net uptake of CO2 because of active photosynthesis by the macroalgae (Jiang et al., 2013). In contrast, knowledge about in situ carbonate chemistry in beds of Sargassum algae is limited (e.g., Tokoro et al., 2019). The present study, however, has shown that a bed of Sargassum algae takes up atmospheric CO2 over a diurnal cycle during productive periods of the year.
Our results showed that metabolism and water exchange regulated the diurnal variations in DIC and fCO2 in the macroalgal bed. Our mass-balance model analyses suggested that the high rate of water inflow from the outside the bed strongly affected DIC concentrations and fCO2 in the macroalgal bed (Fig. 3a, f). The decrease in the DIC concentration of the macroalgal bed was moderated by water exchange during the day. The high rate of water exchange reduced the difference in FCO2 between the inside and outside of the macroalgal beds (Fig. 7). Conversely, water characterized by low DIC and fCO2 values was efficiently exported from the macroalgal bed to the surrounding water (Fig. 7). Our findings therefore suggested that macroalgal beds can create areas of adjacent water that serve as CO2 sinks. Previous studies have proposed that a canopy of the kelp genus Macrocystis dampens water exchange (Rosman et al., 2007), and the residence time of water within kelp beds can reach several days (Jackson and Winant, 1983; Delille et al., 2009). In contrast, the exposed side of a kelp bed is very much affected by the advection of offshore water (Koweek et al., 2017). Water exchange rates are affected by the surface area of beds, canopy development, topography, and hydrological conditions.
The seasonality of the growth of macroalgae regulates the seasonal variations in carbonate chemistry and sink–source behavior (Delille et al., 2009; Koweek et al., 2017). Annual fluctuations of the surface area of kelp beds affect interannual variations in air–water CO2 fluxes in adjacent water bodies (Ikawa and Oechel, 2015). In the present study, we focused on how daily carbon budgets were related to macroalgal metabolism and hydrological conditions during productive periods. The biomass of Sargassum algae fluctuates seasonally and increases in winter (from November to April) around the present study site (Yoshida et al., 2001). Future studies should assess the seasonal variability in carbonate chemistry in Sargassum beds.
The homogenous buffer factor (β) is a general and helpful tool that can be used to identify the main processes that affect carbonate chemistry dynamics (e.g., Frankignoulle, 1994). Frankignoulle (1994) found the relationship × %Corg, where %Corg is the percent change of the DIC concentration due to photosynthesis and respiration. By using this equation, we calculated the %Corg to be 96 % and 88 % in February and March, respectively (Fig. 4). The results therefore indicate that NCP was the main regulator of carbonate chemistry, and the contribution of NCC was relatively small. This conclusion is consistent with the results of the field-bag experiments (Table 1).
4.3 Community metabolism in the macroalgal bed
Macroalgal NCP values in the present study (302–1378 mmol C m−2 d−1) were comparable to those in a sub-Arctic kelp bed (∼1250 mmol C m−2 d−1; Delille et al., 2009) and to gross primary production in a Macrocystis kelp bed in California (∼570 mmol C m−2 d−1; Towle and Pearse, 1973; Jackson, 1987) and in an Ecklonia kelp bed (464 mmol C m−2 d−1; Randall et al., 2019); they were much larger than the NCP values in a calcareous macrophyte bed (19 mmol C m−2 d−1; Bensoussan and Gattuso, 2007), in temperate maerl beds (−38 mmol C m−2 d−1; Martin et al., 2007), and on a coral reef dominated by green and red algae (−112 to 61 mmol C m−2 d−1; Falter et al., 2001). The suppression of macroalgal R by low water temperatures during the productive winter can explain the relatively high NCP values observed at our study site (Tables 1 and S1). The macroalgal NCP value during March was 4 times higher than the value during February in the present study (Table 1). Irradiance, length of the photoperiod, and growth phase collectively control the temporal variations in macroalgal NCP. In the present study, both surveys were conducted during the productive period, but the difference in the averaged biomass per individual S. horneri used for the field-bag experiments (February – 353 g WW; March – 260 g WW) may indicate a difference in growth phase.
The relative growth rates (% d−1) of S. horneri were calculated to be 1.1–7.3 % d−1 based on the ratio of growth (= NCP − NDR) to biomass (Table S1). To calculate biomass, we assumed that the water content was 85 % of the wet weight and that carbon content was 30 % of the dry weight (Watanabe et al., unpublished data). These relative growth rates were comparable to estimates based on biomass changes of S. horneri (around 4 % d−1; Gao and Hua, 1997; Choi et al., 2008) and S. muticum (∼10 % d−1; Pedersen et al., 2005).
The estimated uncertainties of NCC and NCP derived from the measurement precision of TAlk and DIC were ∼13 mmol C m−2 d−1 and ∼26 mmol C m−2 d−1, respectively. These uncertainties were similar to NCC values (macroalgae – 11–21 mmol C m−2 d−1; phytoplankton – −12–3 mmol C m−2 d−1) and phytoplankton NCP values (7–22 mmol C m−2 d−1; Table 1). It is therefore difficult to discuss NCC values and phytoplankton NCP values quantitatively, but these values were substantially lower than macroalgal NCP values in this study. Increasing the incubation time in the field-bag experiments should help to reduce these uncertainties.
4.4 Implications for the CO2 sequestration function of macroalgae
Macroalgal beds are considered to be potential carbon-donor sites in the context of blue carbon sequestration (Krause-Jensen et al., 2018). The release and subsequent export of particulate macroalgal carbon (e.g., entire thalli and fragments) via physical processes would contribute to CO2 sequestration (Krause-Jensen and Duarte, 2016; Filbee-Dexter et al., 2018; Pessarrodona et al., 2018; Kokubu et al., 2019; Pedersen et al., 2020; Fig. 2). The export of recalcitrant DOC from macroalgal beds is also anticipated to be an important pathway of CO2 sequestration (Wada and Hama, 2013; Barrón et al., 2014; Reed et al., 2015). A first-order assessment has suggested that almost 70 % of global macroalgal carbon sequestration is attributable to DOC export to depths below the mixed layer (Krause-Jensen and Duarte, 2016). Our results showed that a Sargassum bed released a substantial amount of RDOC, which was rapidly exported from the habitat to the offshore. The maximum residence time of dissolved matter in the study's oceanographic basin is between 95 and 218 d depending on the season (Balotro et al., 2002), indicating that macroalgal RDOC can be exported to the outside of the Seto Inland Sea and to depths below the mixed layer via vertical mixing.
The decrease in fCO2 due to macroalgal DIC uptake directly controls the influx of atmospheric CO2 into macroalgal habitats and the waters surrounding them. The present study showed that the metabolism of Sargassum algae mediated the production of low-DIC and low-fCO2 water, which was rapidly exported to outside the habitat. Because macroalgae commonly inhabit rocky reefs facing the open ocean, macroalgal metabolism may affect a wide range of water bodies surrounding rocky reef habitats (e.g., Ikawa and Oechel, 2015). The CO2 sequestration function of macroalgae found in habitats where macroalgae-affected water easily diffuses offshore has been overlooked.
Studies of the role of macroalgae in CO2 sequestration should use field observations and coupled ecological–physical models to assess the spatial spread and fate of DOC and low-fCO2 waters derived from macroalgal habitats (Kuwae et al., 2019; Macreadie et al., 2019). Because coastal primary producers other than macroalgae can also be a source of low-fCO2 and high-DOC waters, separately analyzing the fate of these waters would help shed light on the role of these ecosystems. Seasonal variations in oceanographic and climatic conditions regulate the transport of waters affected by macroalgae. Such studies will lead to a better understanding of the role of macroalgae in sequestering blue carbon and thereby mitigating global climate change.
The present study showed that macroalgal metabolism and lateral carbon flows regulated carbon budgets and air–water CO2 exchange in a temperate macroalgal bed and its surrounding water. Macroalgae took up DIC via photosynthesis and released large amounts of DOC to the offshore waters adjacent to the bed. Hydrological water exchange enhanced the lateral carbon flows and the spread of low-fCO2 and high-DOC water mediated by macroalgal metabolism. Our findings suggest that macroalgal beds have the potential to create areas of adjacent water that serve as CO2 sinks. These results suggest the need for future research to assess the areal extent and fate of macroalgae-mediated low-fCO2 and high-DOC waters.
The data set used in this study can be obtained from Zenodo (https://doi.org/10.5281/zenodo.3715876; Watanabe et al., 2020).
The supplement related to this article is available online at: https://doi.org/10.5194/bg-17-2425-2020-supplement.
KW, GY, MH, YU, and TK conceived the study. KW, GY, MH, HM, and TK collected the samples. KW and HM conducted the laboratory analyses. KW and TK processed the data. KW and TK wrote the paper, with substantial input from the other authors.
The authors declare that they have no conflict of interest.
We thank Atsushi Kajita, Koji Manabe, and Shinjiro Sueyoshi for help in field observations and Naoko Umegaki, Hikaru Kimishima, and Ryoko Makino for chemical analyses. Finally, we thank Albert Pessarrodona Silvestre and Dorte Krause-Jensen as reviewers for their useful comments that contributed to the development of the paper.
This research has been supported by Grants-in-Aid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science (grant nos. JP18H04156, 19K20500, and 19K12295).
This paper was edited by Jean-Pierre Gattuso and reviewed by Dorte Krause-Jensen and Albert Pessarrodona Silvestre.
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