Harmful algal blooms threaten the water quality of many eutrophic and hypertrophic lakes and cause severe ecological and economic damage worldwide. Dense blooms often deplete the dissolved CO2 concentration and raise pH. Yet, quantitative prediction of the feedbacks between phytoplankton growth, CO2 drawdown and the inorganic carbon chemistry of aquatic ecosystems has received surprisingly little attention. Here, we develop a mathematical model to predict dynamic changes in dissolved inorganic carbon (DIC), pH and alkalinity during phytoplankton bloom development. We tested the model in chemostat experiments with the freshwater cyanobacterium Microcystis aeruginosa at different CO2 levels. The experiments showed that dense blooms sequestered large amounts of atmospheric CO2, not only by their own biomass production but also by inducing a high pH and alkalinity that enhanced the capacity for DIC storage in the system. We used the model to explore how phytoplankton blooms of eutrophic waters will respond to rising CO2 levels. The model predicts that (1) dense phytoplankton blooms in low- and moderately alkaline waters can deplete the dissolved CO2 concentration to limiting levels and raise the pH over a relatively wide range of atmospheric CO2 conditions, (2) rising atmospheric CO2 levels will enhance phytoplankton blooms in low- and moderately alkaline waters with high nutrient loads, and (3) above some threshold, rising atmospheric CO2 will alleviate phytoplankton blooms from carbon limitation, resulting in less intense CO2 depletion and a lesser increase in pH. Sensitivity analysis indicated that the model predictions were qualitatively robust. Quantitatively, the predictions were sensitive to variation in lake depth, DIC input and CO2 gas transfer across the air-water interface, but relatively robust to variation in the carbon uptake mechanisms of phytoplankton. In total, these findings warn that rising CO2 levels may result in a marked intensification of phytoplankton blooms in eutrophic and hypertrophic waters.
Citation: Verspagen JMH, Van de Waal DB, Finke JF, Visser PM, Van Donk E, Huisman J (2014) Rising CO2 Levels Will Intensify Phytoplankton Blooms in Eutrophic and Hypertrophic Lakes. PLoS ONE 9(8): e104325. doi:10.1371/journal.pone.0104325
Editor: Hans G. Dam, University of Connecticut, United States of America
Received: June 14, 2013; Accepted: June 17, 2014; Published: August 13, 2014
Copyright: © 2014 Verspagen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research was supported by grant 854.10.006 of the Earth and Life Sciences Foundation (ALW), which is subsidized by the Netherlands Organization for Scientific Research (NWO). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Since the start of the industrial revolution, atmospheric CO2 concentrations have increased from 275 to 400 ppm CO2, and climate change scenarios predict that atmospheric CO2 will further increase . Enhanced dissolution of CO2 will lower the pH of aquatic ecosystems , . However, CO2 in freshwater ecosystems does not only originate from dissolution of atmospheric CO2, but also from mineralization of organic carbon obtained from terrestrial sources in the surrounding watershed . Mineralization of organic carbon causes CO2 supersaturation in many lakes, in some cases even reaching CO2 levels exceeding 10,000 ppm –.
Phytoplankton fix CO2 for photosynthesis, and many species can also utilize bicarbonate as a carbon source –. Assimilation of inorganic carbon by dense phytoplankton blooms can deplete the dissolved CO2 concentration –, sometimes down to levels below 1 ppm , , so that these waters become severely CO2-undersaturated. CO2 depletion will cause an increase in pH , , . Indeed, in eutrophic lakes with dense phytoplankton blooms, pH easily exceeds values of 9 , , and can reach values as high as 11 in shallow hypertrophic lakes .
The combination of high pH values and CO2 depletion in freshwaters is often associated with cyanobacterial blooms , . Several of the cyanobacterial species that commonly dominate these blooms are capable of producing toxic substances , . Consequently, cyanobacterial blooms threaten the water quality of many freshwater lakes and brackish waters around the world, including Lake Erie in USA-Canada , Lake Taihu in China , , Lake Biwa in Japan , Lake Victoria in Africa , , the Baltic Sea in Northern Europe , , and many other ecologically and economically important lakes, rivers and estuaries , , , . Cyanobacterial blooms are expected to benefit from global warming –. The response of cyanobacteria to rising CO2 concentrations, however, is less well understood, although it is clear that there is a strong interaction between cyanobacterial bloom development and CO2 availability.
As an illustration, Fig. 1 provides data from Lake Volkerak, a large eutrophic lake in The Netherlands , . In winter and spring, CO2 concentrations in Lake Volkerak largely exceed the CO2 concentrations that would be predicted from equilibrium with the atmosphere, and hence the lake is supersaturated with CO2. In summer and early fall, however, Lake Volkerak is covered by dense blooms of the harmful cyanobacterium Microcystis , . The photosynthetic activity of these blooms depletes the CO2 concentration, such that the lake becomes undersaturated with CO2 in summer while the pH rises to values above 9 for several months (Fig. 1, Text S1).
(A) Changes in phytoplankton population density (strongly dominated by the cyanobacterium Microcystis) and measured dissolved CO2 concentration ([CO2]) during two consecutive years. The dashed line is the expected dissolved CO2 concentration ([CO2*]) when assuming equilibrium with atmospheric pCO2. Dark shading indicates that the lake is supersaturated with CO2, while light shading indicates undersaturation. (B) Changes in pH, bicarbonate and total DIC concentration. Sampling details are described in Text S1.
Hence, there is a strong and complex coupling between phytoplankton growth and the inorganic carbon chemistry of aquatic ecosystems that may lead to CO2 depletion during dense blooms, even in lakes that would otherwise be supersaturated with CO2. This biological-chemical coupling is further complicated by several additional feedbacks. For instance, dense phytoplankton blooms not only deplete CO2 and enhance pH but also increase the turbidity of the water column as a result of self-shading, thereby reducing light available for carbon fixation by photosynthesis , . Moreover, nutrient uptake by dense blooms also affects alkalinity –, which in turn feeds back upon pH and the speciation of dissolved inorganic carbon (DIC). Given the pH and total DIC concentration, it is straightforward to calculate the CO2, bicarbonate and carbonate concentrations –. However, we still lack an integrative understanding that incorporates the different feedback loops to enable quantitative prediction of the changes in DIC concentration and pH during phytoplankton bloom development. Yet, such an integrative approach will be required to assess how rising CO2 concentrations will affect phytoplankton blooms and carbon sequestration in aquatic systems.
In this study, we investigate the dynamic feedbacks between phytoplankton growth, DIC, alkalinity, pH and light during phytoplankton bloom development. Our study specifically focuses on eutrophic and hypertrophic waters, where an excess of mineral nutrients provides ideal conditions for phytoplankton blooms. We incorporate standard inorganic carbon chemistry into a mathematical model of phytoplankton growth with CO2, bicarbonate and light as limiting resources. We test the model in controlled laboratory experiments at different pCO2 levels and alkalinities using the harmful cyanobacterium Microcystis aeruginosa, a cosmopolitan and often toxic species that develops dense blooms in Lake Volkerak and many other eutrophic lakes worldwide –, , . Our model fits were in good agreement with the experimental results, and show that the coupling between phytoplankton growth and inorganic carbon chemistry is strongly affected by the CO2 level. Subsequently, we use the experimentally validated model to explore how phytoplankton blooms in eutrophic lakes may respond to rising CO2 availability.
Our model builds upon a long tradition of model studies in phytoplankton ecology –, extending these earlier studies by the incorporation of dynamic changes in inorganic carbon availability, alkalinity and pH induced by phytoplankton blooms. The model considers a well-mixed water column, illuminated from above, with a growing phytoplankton population that is homogeneously distributed over depth. Here we introduce the key assumptions, while the model is described in full detail in Text S2 (for chemostats) and Text S3 (for lakes).
Phytoplankton population dynamics
In this study, we focus on eutrophic and hypertrophic ecosystems where all nutrients are in excess. Hence, the specific growth rate of phytoplankton does not become limited by nutrients but depends only on its cellular carbon content. The cellular carbon content is a dynamic variable, which increases by the photosynthetically-driven uptake of CO2 and bicarbonate, while it decreases by respiration and by dilution of the cellular carbon content due to population growth. More precisely, let X denote the population density of the phytoplankton, and let Q denote its cellular carbon content. Changes in phytoplankton population density and its carbon content can then be described by:(1)(2)where µ(Q) is the specific growth rate of the phytoplankton as function of its cellular carbon content, m is the specific loss rate (e.g., by background mortality, grazing, sedimentation), uCO2 and uHCO3 are the uptake rates of CO2 and bicarbonate, respectively, and r is the respiration rate.
We assume that the specific growth rate increases with the cellular carbon content of the phytoplankton, which require a minimum cellular carbon content in order to function (i.e., µ(QMIN) = 0) and reach their maximum specific growth rate when satiated with carbon (i.e., µ(QMAX) = µMAX). Uptake rates of CO2 (uCO2) and bicarbonate (uHCO3) are increasing but saturating functions of the ambient CO2 and bicarbonate concentration according to Michaelis-Menten kinetics, and are suppressed when cells become satiated with carbon . The energy for carbon assimilation comes from photosynthesis, and therefore depends on light availability. The underwater light environment is described by Lambert-Beer’s law, taking into account that a growing phytoplankton population gradually increases the turbidity of the water column through self-shading and thereby reduces the light available for further photosynthesis , . We assume that the respiration rate (r) increases with the cellular carbon content, approaching maximum values when cells become satiated with carbon . The mathematical equations describing these relationships are presented in Text S2.
To assess to what extent phytoplankton growth is limited by carbon, we introduce a simple relative measure of the inorganic carbon availability for photosynthesis (fC):(3)where uMAX,CO2 and uMAX,HCO3 are the maximum uptake rates of carbon dioxide and bicarbonate, respectively, and HCO2 and HHCO3 are their half-saturation constants. We note that 0≤fC≤1. The level of carbon limitation (LC) can then be defined as the reduction in carbon uptake due to low carbon availability: LC = (1−fC)×100%. Accordingly, if CO2 and bicarbonate are both available in saturating concentrations, LC will be close to 0%. Conversely, if CO2 and bicarbonate are available only in trace amounts, LC approaches 100%.
Dissolved inorganic carbon, alkalinity and pH
On the timescales used in our model (ranging from minutes to days) the speciation of dissolved inorganic carbon is essentially in equilibrium with alkalinity and pH. Therefore, let [DIC] denote the total concentration of dissolved inorganic carbon. Changes in [DIC] can be described by:(4)
The first term on the right-hand side of Eqn (4) describes changes in the DIC concentration due to the influx ([DIC]IN) and efflux of water containing DIC, where D is the dilution rate. The second term describes exchange of CO2 gas with the atmosphere, where gCO2 is the CO2 flux across the air-water interface (also known as the carbon sequestration rate) and division by zMAX converts the CO2 flux per unit surface into a volumetric CO2 change. The third term describes how the DIC concentration increases through respiration (r) and decreases through uptake of CO2 (uCO2) and bicarbonate (uHCO3) by phytoplankton.
The CO2 flux across the air-water interface is proportional to the difference between the dissolved CO2 concentration that would be attained in equilibrium with the atmospheric pressure ([CO2*]) and the actual dissolved CO2 concentration , :(5)where v is the gas transfer velocity. The equilibrium value [CO2*] is calculated from Henry’s law, i.e., [CO2*] = K0 pCO2, where pCO2 is the partial pressure of CO2 in air and K0 is the solubility constant of CO2 gas in water. In our experiments, gas exchange will increase with the gas flow rate (a). Hence, we assume v = b a, where b is a constant of proportionality reflecting the efficiency of gas exchange.
Changes in pH depend on alkalinity, which is a measure of the acid-neutralizing capacity of water. In our experiments, alkalinity is dominated by dissolved inorganic carbon and inorganic phosphates :(6)
We note from Eqn (6) that changes in the concentration of dissolved CO2 do not change alkalinity. Furthermore, uptake of bicarbonate for photosynthesis is accompanied by the release of a hydroxide ion or uptake of a proton, and therefore does not change alkalinity either. Hence, carbon assimilation by phytoplankton does not affect alkalinity . However, nitrate, phosphate and sulfate assimilation are accompanied by proton consumption to maintain charge balance, and thus increase alkalinity –. More specifically, both nitrate and phosphate uptake increase alkalinity by 1 mole equivalent, whereas sulfate uptake increases alkalinity by 2 mole equivalents . Hence, changes in alkalinity can be described as:(7)where ALKIN is the alkalinity of the water influx, and uN, uP and uS are the uptake rates of nitrate, phosphate and sulfate by the growing phytoplankton population. The model keeps track of the nitrate, phosphate and sulfate concentration.
At each time step, the dissolved CO2, bicarbonate and carbonate concentration and pH are calculated from [DIC] and alkalinity (Text S2).
Materials and Methods
We tested the model using two strains of the freshwater cyanobacterium Microcystis aeruginosa. Strain Microcystis CYA140 was obtained from the Norwegian Institute for Water Research (NIVA). Strain Microcystis HUB5-2-4 was obtained from the Humboldt University of Berlin, Germany. Both Microcystis strains grow as single cell populations. Although all culture equipment was autoclaved prior to the experiments, we were not able to sustain axenic conditions. However, regular microscopic inspection confirmed that abundances of heterotrophic bacteria remained low (<0.1% of the total biomass) for the entire duration of the experiments.
The experiments were carried out in laboratory-built chemostats specifically designed for phytoplankton studies , , . Each chemostat consisted of a flat culture vessel illuminated from one side with a constant incident light intensity of IIN = 50±1 µmol photons m−2 s−1 provided by white fluorescent tubes (Philips PL-L 24W/840/4P, Philips Lighting, Eindhoven, The Netherlands). The chemostats had an optical path length (“mixing depth”) of zMAX = 5 cm, and an effective working volume of 1.7 L. The chemostats were supplied with a nutrient-rich mineral medium  to prevent nutrient limitation during the experiments. Under conditions of nutrient excess, phytoplankton population densities tend to become much higher in laboratory chemostats where phytoplankton is concentrated within only 5 cm depth than in lakes where the phytoplankton population is dispersed over several meters depth , . This scaling rule implies that nutrient concentrations have to be much higher in mineral media of small-scale laboratory chemostats than in eutrophic lakes to sustain these high population densities. The chemostats were maintained at a constant temperature using a metal cooling finger connected to a Colora thermocryostat, and were aerated with sterilized (0.2 µm Millex-FG Vent Filter, Millipore, Billerica, MA, USA) N2 gas enriched with different CO2 concentrations using Brooks Mass Flow Controllers (Brooks Instrument, Hatfield, PA, USA). The gas mixture was dispersed from the bottom of the chemostat vessel in fine bubbles at a constant gas flow rate (a) of 25 L h−1.
First, we studied dynamic changes in inorganic carbon chemistry and pH in six chemostats without any phytoplankton, to assess whether the model adequately described the dissolution of CO2 and subsequent dynamic changes in inorganic carbon chemistry. These auxiliary experiments are described in Text S4.
Subsequently, we ran two chemostat experiments with Microcystis CYA140 to investigate dynamic changes in phytoplankton growth, inorganic carbon chemistry, alkalinity and pH. The first chemostat was provided with a low pCO2 of 200 ppm in the gas flow and 0.5 mmol L−1 NaHCO3 in the mineral medium. The second chemostat was provided with a high pCO2 of 1,200 ppm in the gas flow and 2.0 mmol L−1 NaHCO3 in the mineral medium. Both chemostats had a dilution rate of D = 0.011 h−1. The chemostats were sampled every other day, from the inoculation of a small number of Microcystis CYA140 cells to steady state with high population densities.
Next, we studied the steady states of six chemostats of Microcystis HUB5-2-4 along a gradient from carbon-limited to light-limited conditions. The chemostats had a dilution rate of D = 0.00625 h−1, and were provided with different pCO2 concentrations in the gas flow (0.5, 50, 100, 400 or 2,800 ppm CO2) and two different NaHCO3 concentrations in the mineral medium (0.5 or 2.0 mmol L−1). The steady states were monitored for at least ten days.
The incident light intensity (IIN) and the light intensity transmitted through the chemostat vessel (IOUT) were measured with a LI-COR LI-250 quantum photometer (LI-COR Biosciences, Lincoln, NE, USA) at 10 randomly chosen positions on the front and back surface of the chemostat vessel, respectively. Background turbidity (Kbg) was calculated from the light transmission through chemostat vessels without phytoplankton using Lambert-Beer’s law, as Kbg = ln(IIN/IOUT)/zMAX.
DIC concentrations were determined by sampling 15 mL of culture suspension, which was immediately filtered over 0.45 µm membrane filters (Whatman, Maidstone, UK). DIC was subsequently analyzed by phosphoric acid addition on a Model 700 TOC Analyzer (OI Corporation, College Station, TX, USA), with a detection limit of 0.15 ppm. Temperature and pH were measured with a SCHOTT pH meter (SCHOTT AG, Mainz, Germany). Concentrations of dissolved CO2, bicarbonate and carbonate were calculated from DIC and pH , based on the dissociation constants of inorganic carbon corrected for temperature and salinity (Table S2.1 in Text S2). Alkalinity was determined in a 50 mL sample that was titrated in 0.1 to 1 mL steps with 10 mmol L−1 HCl to a pH of 3.0. The alkalinity was subsequently calculated using Gran plots .
Residual nitrate and phosphate concentrations in the chemostats were determined in triplicate by sampling 15 mL of culture suspension, which was immediately filtered over 0.45 µm membrane filters (Whatman, Maidstone, UK) and the filtrate was stored at −20°C. Nitrate concentrations were analyzed using a Skalar SA 400 autoanalyzer (Skalar Analytical B.V., Breda, The Netherlands), and phosphate concentrations were analyzed spectrophotometrically .
Phytoplankton population density, both as cell numbers and total biovolume, was determined in triplicate using a Casy 1 TTC cell counter with a 60 µm capillary (Schärfe System GmbH, Reutlingen, Germany). Cell size varied considerably during the experiments, ranging from 31–66 µm3 cell−1 in Microcystis CYA140 and from 25–50 µm3 cell−1 in Microcystis HUB5-2-4. We therefore used the total biovolume (i.e. the summed volume of all cells per litre of water) as a measure of phytoplankton population density.
Samples for cellular carbon, nitrogen, phosphorus and sulfur content were pressurized at 10 bar to collapse the gas vesicles of Microcystis and subsequently centrifuged for 15 min at 2,000 g. After discarding the supernatant, the pellet was resuspended in demineralised water, and centrifuged for 5 min at 15,000 g. The supernatant was discarded, pellets were stored at −20°C and subsequently freeze-dried and weighted to determine dry weight. The carbon, nitrogen and sulfur content of homogenised freeze-dried cell powder were analysed using a Vario EL Elemental Analyzer (Elementar Analysensysteme GmbH, Hanau, Germany). To determine the phosphorus content, cells were oxidized with potassium persulfate for 1 h at 100°C , and phosphate concentrations were subsequently analyzed spectrophotometrically .
To calculate the carbon sequestration rate of the experiments at steady state, we solved Eqns (1), (2) and (4) for zero. This yields:(8)where we assumed that the specific loss rate of the phytoplankton was governed by the dilution rate of the chemostat (i.e., m = D). This equation shows that, at steady state, the carbon sequestration rate equals the net enhancement of the DIC concentration plus the carbon fixation rate of the phytoplankton population.
System parameters such as incident light intensity, mixing depth of the chemostats, composition of the mineral medium, dilution rate and CO2 concentration in the gas flow were measured prior to and/or during the experiments. Some phytoplankton parameters were measured experimentally, while others were estimated from fits of the model predictions to time courses of the experimental variables following the same procedures as in earlier studies , . An overview of all parameter estimates is given in Text S2.
Extrapolation to lakes
Chemostats provide ideal systems to test models under highly controlled conditions. They operate at the laboratory scale, with parameter settings tuned to the small size of the chemostat vessel. To extrapolate the model predictions to natural waters, we therefore adapted several model assumptions. Phytoplankton parameters were still based on our laboratory experiments with Microcystis HUB5-2-4. However, we used physical and chemical parameter settings typical for the summer situation in eutrophic lakes based on our data from Lake Volkerak, The Netherlands . For instance, the mixing depth was increased from a chemostat of only 5 cm deep to a lake of 5 m deep. The very high phosphate and nitrate concentrations in the mineral medium of the chemostat were reduced to a lower (but still fairly high) phosphate concentration of 15 µmol L−1 and nitrate concentration of 150 µmol L−1, representative for hypertrophic lakes dominated by cyanobacterial blooms , , –. The high influx of CO2 gas into the chemostat vessel was replaced by a low gas transfer velocity across the air-water interface of lakes , , . Full implementation of the lake model is described in Text S2 and Text S3.
We performed a sensitivity analysis to assess how variation in the model parameters would affect the model predictions. In this analysis, we focus on low-alkaline lakes (ALKIN = 0.5 mEq L−1), since they are more sensitive to rising atmospheric CO2 concentrations than high-alkaline lakes. The sensitivity analysis investigates how the model predictions were affected by variation in two input parameters: (i) the atmospheric CO2 level and (ii) a second model parameter of choice. In contrast to traditional one-factor-at-a-time (OAT) sensitivity analysis, this two-dimensional approach may reveal possible interactions between the two model parameters . For instance, model predictions might be more sensitive to parameter changes at low than at high atmospheric CO2 levels.
In addition, we calculated the normalized sensitivity coefficient (SC), which is a local sensitivity index that quantifies the relative change in model output Y with respect to a relative change in input parameter Z :(9)
The normalized sensitivity coefficient is dimensionless, and allows comparison between input and output parameters independent of their units of measurement. |SC|>>1 implies that the model prediction is very sensitive to a change in the input parameter, whereas |SC|<<1 implies that the model prediction is rather insensitive to a change in the input parameter. We based the calculation of SC on a 1% increment of the input parameter. The sensitivity coefficient was calculated at two atmospheric CO2 levels, the present-day level of 400 ppm and an elevated level of 750 ppm predicted for the year 2150 by the RCP6 scenario of the Fifth Assessment Report of the IPCC .
Dynamic changes during phytoplankton growth
We studied dynamic changes in inorganic carbon chemistry during the growth of Microcystis CYA140 in two chemostats that differed with respect to the pCO2 level in the gas flow and the bicarbonate concentration in the medium (Fig. 2). In both chemostats, the population density increased after inoculation, while light penetration (IOUT) decreased due to shading by the growing Microcystis populations, until steady state was reached after ∼30 days (Figs. 2A and 2B). At high pCO2 the population density became two times higher and light penetration decreased more strongly than at low pCO2.
Left panels: Chemostat experiment with low pCO2 of 200 ppm in the gas flow and 500 µmol L−1 bicarbonate in the mineral medium. Right panels: Chemostat experiment with high pCO2 of 1,200 ppm in the gas flow and 2,000 µmol L−1 bicarbonate in the mineral medium. Both chemostats were inoculated with Microcystis CYA140. (A, B) Population density (expressed as biovolume) and light intensity penetrating through the chemostat (IOUT), (C, D) dissolved CO2, bicarbonate and carbonate concentrations, (E, F) total DIC concentration and pH, and (G, H) alkalinity (ALK) and concentrations of dissolved inorganic nitrogen (DIN) and phosphorus (DIP). Symbols represent measurements, lines show the model fits. The model and its parameter values are detailed in Text S2.
Phytoplankton growth impacted DIC, pH and alkalinity in both chemostats, but in a different way. With a low pCO2 in the gas flow, the growing phytoplankton population depleted the dissolved CO2 concentration over almost two orders of magnitude, from 10 to 0.2 µmol L−1, while the bicarbonate concentration varied between 600 and 900 µmol L−1 (Fig. 2C). At high pCO2, the dissolved CO2 concentration was much less depleted, while the bicarbonate concentration doubled from 2,000 µmol L−1 at inoculation to 4,000 µmol L−1 at steady state (Fig. 2D). The strong CO2 depletion raised the pH from 8 to 10 at low pCO2 (Fig. 2E), while the pH increased only to ∼8.5 at high pCO2 (Fig. 2F). The increase in pH mediated a shift in carbon speciation in both chemostats, although the shift was more dramatic at low pCO2 (Fig. 2C and 2D). In particular, the carbonate concentration increased to ∼45% of the total DIC at low pCO2, while it remained at only 4% at high pCO2. The total DIC concentration increased from 600 to 1,000 µmol L−1 at low pCO2 (Fig. 2E), and from 2,100 to 4,200 µmol L−1 at high pCO2 (Fig. 2F).
Despite the increase in total DIC, the phytoplankton experienced considerable carbon limitation (LC = 44%) in the experiment at low pCO2. This was primarily due to depletion of the dissolved CO2 concentration. Carbonate is unavailable for uptake, while our model estimated a half-saturation constant for bicarbonate of 75 µmol L−1 (Table S2.3 in Text S2), indicating that the bicarbonate uptake rate was essentially saturated with bicarbonate throughout the experiment. At high pCO2, carbon limitation was negligible (LC = 2%), and growth was primarily limited by the low availability of light. At steady state, the light intensity penetrating through the chemostat vessel (IOUT) was only 0.8 µmol photons m−2 s−1 (Fig. 2B).
The growing phytoplankton population reduced the residual nitrate and phosphate concentration, yet nitrate and phosphate remained available at saturating concentrations of >10 mmol N L−1 and >180 µmol P L−1, respectively (Fig. 2G and 2H). Hence, nitrate and phosphate were not depleted to limiting levels. However, uptake of nitrate, phosphate and sulfate by phytoplankton consumed H+ ions and thereby increased alkalinity in both chemostats (Fig. 2G and 2H). Since a larger population density consumes more nutrients, alkalinity increased more strongly in the high pCO2 than in the low pCO2 treatment. The model fits captured the coupling between phytoplankton growth, carbon availability, nutrients, light, pH and alkalinity quite well at both low and high pCO2 levels (Fig. 2).
Separation of time scales
Because of the relatively high dimensionality of our model, formal mathematical analysis of the existence, uniqueness and stability of the equilibrium point is not straightforward. Therefore, we explored the full phase space of the model by extensive numerical simulations. This did not reveal any indications for alternative stable states or non-equilibrium dynamics. Instead, we always found at most one unique positive equilibrium point that was locally and globally stable whenever it existed.
Two examples are given in Fig. 3, where we used the calibrated model to investigate trajectories of dissolved CO2 and population density from a range of different initial conditions. Interestingly, the trajectories show that the dynamics operated at two distinct time scales: fast chemical dynamics and slow biological dynamics. The inorganic carbon chemistry equilibrated with the standing population density within a few hours, as indicated by the horizontal parts of the trajectories in Fig. 3. These rapid dynamics are consistent with the inorganic carbon chemistry in our chemostat experiments without phytoplankton, which also equilibrated within 1–4 hours (Fig. S4.1 in Text S4). Subsequently, the population density slowly converged to equilibrium within a time span of several weeks. These slow dynamics are indicated in Fig. 3 by the thick curved parts of the trajectories, which ultimately lead to the equilibrium point. Hence, the inorganic carbon chemistry rapidly adjusted to the standing population, and subsequently tracked the slower changes in population density.
Trajectories predicted by the model for chemostats with (A) low pCO2 of 200 ppm in the gas flow and 500 µmol L−1 bicarbonate in the mineral medium, and (B) high pCO2 of 1,200 ppm in the gas flow and 2,000 µmol L−1 bicarbonate in the mineral medium. The trajectories start from a series of different initial conditions, and all converge to the same equilibrium point. Arrows indicate the direction of the trajectories. The model assumes species parameters specific for Microcystis CYA140, and is detailed in Text S2.
We investigated steady-state patterns of phytoplankton abundance and inorganic carbon chemistry using six chemostats of Microcystis HUB5-2-4 (Fig. 4). The steady-state population density increased with pCO2, demonstrating that it was limited by the supply of inorganic carbon. The population density leveled off when carbon limitation was alleviated at pCO2>200 ppm (Fig. 4A). At pCO2 levels <1 ppm, a low DIC concentration of 0.5 mmol L−1 in the mineral medium provided insufficient inorganic carbon, whereas a higher DIC concentration of 2.0 mmol L−1 was sufficient to sustain a steady-state population density. At pCO2 levels >100 ppm, the influx of DIC supplied by the mineral medium was small compared to the influx of CO2 supplied by the high gas flow rate, such that the four-fold difference in DIC concentration in the mineral medium had little effect on the steady-state population density.
Steady-state results are shown for 6 chemostats with Microcystis HUB5-2-4 exposed to different pCO2 levels in the gas flow and two different bicarbonate concentrations in the mineral medium (0.5 or 2.0 mmol L−1). (A) Phytoplankton population density (expressed as biovolume), (B) light intensity penetrating through the chemostat (IOUT), (C) dissolved CO2 concentration, (D) bicarbonate concentration, (E) pH, (F) alkalinity, (G) DIC concentration, and (H) carbon sequestration rate. Symbols show the mean (± s.d.) of 5 measurements in each steady-state chemostat, lines show the model fits. For comparison, dashed lines show steady-state patterns predicted for chemostats without phytoplankton. Shading indicates the level of carbon limitation (LC) predicted by the model. The model and its parameter values are detailed in Text S2.
The increase in population density with rising pCO2 reduced light penetration through the chemostats (Fig. 4B), which shifted the growth conditions from carbon limitation at low pCO2 to light limitation at high pCO2. At pCO2 levels <100 ppm, phytoplankton strongly depleted the dissolved CO2 concentration to a stable level of ∼0.1 µmol L−1 (Fig. 4C), while pH was maintained at values around 10 (Fig. 4E). At pCO2 levels >100 ppm, the dissolved CO2 concentration increased and pH decreased with increasing pCO2 (Fig. 4C, E). The pH remained consistently higher in the presence than in the absence of phytoplankton.
Counterintuitively, at pCO2>100 ppm, the bicarbonate concentration became higher in the presence than in the absence of phytoplankton (Fig. 4D), even though phytoplankton consume bicarbonate as inorganic carbon source. This unexpected result is caused by the shift in pH in combination with an increase in alkalinity associated with uptake of nitrate, phosphate and sulfate by the phytoplankton population (Fig. 4F; see also Eqn (7)). An increased alkalinity enhances the storage capacity for bicarbonate and carbonate in the system. The alkalinity, bicarbonate concentration and total DIC concentration all showed a similar increase with rising pCO2 as the phytoplankton population density (compare Figs. 4D, F, G with Fig. 4A). At pCO2>200 ppm, 70–80% of the total amount of carbon in the system was in phytoplankton biomass while 20–30% of the total carbon was DIC.
The carbon sequestration rate also showed a similar increase with rising pCO2 as the DIC concentration and phytoplankton population density, and leveled off when the population approached its maximum productivity at >200 ppm (Fig. 4H).
The model fits were in good agreement with the observed steady-state patterns in phytoplankton population density, inorganic carbon availability, alkalinity and pH along the entire CO2 gradient.
Extrapolation to lakes
The model was adapted to natural waters to explore the impact of rising atmospheric CO2 levels on phytoplankton blooms in lakes. Although it is difficult to capture the complex dynamics of natural systems, such a modelling exercise may help in understanding the coupling between phytoplankton blooms and inorganic carbon chemistry. As a first step, we investigated steady-state patterns of phytoplankton abundance in low-alkaline lakes, where bicarbonate concentrations are low and phytoplankton growth therefore largely depends on dissolved CO2 as a carbon source. This is a similar situation as in our chemostat experiments, and the model predictions for low-alkaline lakes are therefore qualitatively similar to the results obtained in our chemostats (compare Fig. 4 and Fig. 5). The phytoplankton population can be sustained at pCO2 levels above 0.17 ppm, and is predicted to increase strongly with pCO2 (Fig. 5A). Above 2,000 ppm, a further rise of the pCO2 level no longer enhances the population density, because the high CO2 supply in combination with self-shading in dense phytoplankton blooms has shifted phytoplankton growth from carbon-limited to light-limited conditions (Fig. 5B).
Steady-state predictions of the model evaluated across a wide range of atmospheric pCO2 levels. (A) Phytoplankton population density (expressed as biovolume), (B) light intensity reaching the lake sediment (IOUT), (C) dissolved CO2 concentration, (D) bicarbonate concentration, (E) pH, (F) alkalinity, (G) DIC concentration, and (H) carbon sequestration rate. Shading indicates the level of carbon limitation (LC). For comparison, dashed lines show steady-state patterns predicted for low-alkaline waters without phytoplankton. The model parameters are representative for eutrophic low-alkaline lakes (ALKIN = 0.5 mEq L−1) dominated by the cyanobacterium Microcystis HUB5-2-4. The model and its parameter values are detailed in Text S2 and Text S3.
Over a wide range of pCO2 levels, from 0.17 to 1,000 ppm, phytoplankton blooms exert strong control over the dissolved CO2 concentration and pH, depleting the dissolved CO2 concentration below 0.1 µmol L−1 and raising pH to 10 (Fig. 5C, E). The bicarbonate and total DIC concentration are reduced by the phytoplankton population for pCO2 levels ranging from 0.17 to 1,400 ppm CO2 (Fig. 5D, G). The bicarbonate concentration, total DIC concentration, alkalinity and carbon sequestration rate all increase with rising pCO2, and level off when the phytoplankton population approaches maximum densities (Fig. 5D, F–H). Above 1,000 ppm, phytoplankton blooms exert less control over CO2 availability and pH, and the dissolved CO2 concentration increases while pH decreases with a further rise in pCO2 (Fig. 5C, E).
Figure 6 summarizes the level of carbon limitation and the population density predicted for dense phytoplankton blooms in different eutrophic waters spanning a wide range of alkalinities and pCO2 levels. In line with expectation, the model predicts that carbon limitation of dense phytoplankton blooms will be most pronounced in low-alkaline waters, where CO2 provides the main inorganic carbon source (Fig. 6A). Rising atmospheric pCO2 levels are expected to lead to a strong increase in phytoplankton population density in these low-alkaline waters (Fig. 6B). In lakes with a moderate alkalinity, where bicarbonate can partially supplement growth when CO2 is depleted, carbon limitation is predicted to be less intense but may still play a substantial role (i.e., LC = 10–50%; Fig. 6A). In high-alkaline waters and soda lakes, however, carbon will rarely be limiting at ambient atmospheric pCO2 levels (Fig. 6A). Their large DIC pools provide a sufficient supply of CO2 and bicarbonate to produce high phytoplankton population densities at ambient pCO2 levels (Fig. 6B).
Model predictions of (A) the level of carbon limitation, and (B) phytoplankton population density (expressed as biovolume, in mm3 L−1). The vertical solid line represents the present-day atmospheric CO2 level of ∼400 ppm, while the vertical dashed line shows the atmospheric CO2 level of 750 ppm predicted for the year 2150 by the RCP6 scenario of the Fifth Assessment Report of the IPCC. The model predictions are based on steady-state solutions across a grid of 40×50 = 2,000 simulations, using the model and parameter values detailed in Text S2 and Text S3.
As a first step, we investigated the sensitivity of the model predictions to variation in the half-saturation constant for CO2 uptake (Fig. 7A, B). Note that an increase of the half-saturation constant implies a reduced affinity. All else being equal, an increase in the half-saturation constant for CO2 therefore leads to stronger carbon limitation and lower phytoplankton population densities (Fig. 7A, B). The normalized sensitivity coefficients were small, both at 400 and at 750 ppm (Table 1). A value of SC = 0.10 implies that for a 1% increase in the half-saturation constant, the model predicts only a 0.1% increase in the level of carbon limitation. Hence, the sensitivity of the model predictions to variation in the half-saturation constant for CO2 uptake is relatively low.
Contour plots of the level of carbon limitation (left panels) and steady-state phytoplankton population density (right panels, expressed as biovolume, in mm3 L−1) predicted for different atmospheric pCO2 levels and phytoplankton traits. The phytoplankton traits are (A, B) the half-saturation constant for CO2 uptake (HCO2), (C, D) the half-saturation constant for bicarbonate uptake (HHCO3), (E, F) the maximum CO2 uptake rate (uMAX, CO2), and (G, H) the cellular N:C ratio (cN). The model considers a low-alkaline lake (ALKIN = 0.5 mEq L−1). Vertical lines represent atmospheric CO2 levels of 400 ppm (present-day) and 750 ppm (predicted for the year 2150 by the RCP6 scenario of the IPCC). Horizontal dotted lines represent our default parameter values. The contour plots are based on steady-state solutions across a grid of 40×50 = 2,000 simulations.
The half-saturation constant for bicarbonate shows a similar pattern (Fig. 7C, D).
An increase in the maximum uptake rate of CO2 causes stronger CO2 depletion during phytoplankton blooms, which results in stronger carbon limitation and higher population densities (Fig. 7E, F). Interestingly, comparison of the sensitivity coefficients indicates that changes in the maximum uptake rate of CO2 have a larger effect on the level of carbon limitation than on the phytoplankton population density (Table 1).
Changes in the C:N stoichiometry of phytoplankton cells do not directly affect the growth rates in our model, because we assumed that all nutrients are available at saturating levels. Changes in cellular C:N stoichiometry may have a small indirect effect, however, because nitrate uptake affects alkalinity, and thereby inorganic carbon availability. Hence, as expected, the model predictions are rather insensitive to changes in cellular C:N stoichiometry (Fig. 7G, H; Table 1).
Lake depth has strong effects on the model predictions. In deep lakes, the phytoplankton population is spread out over a large water volume, and will be light-limited in deeper parts of the water column. Hence, all else being equal, CO2 depletion in deep lakes will be less intense, resulting in lower levels of carbon limitation than in shallow lakes (Fig. 8A). Phytoplankton population densities are therefore predicted to respond more strongly to rising pCO2 levels in shallow than in deep lakes (Fig. 8B).
Contour plots of the level of carbon limitation (left panels) and steady-state phytoplankton population density (right panels, expressed as biovolume, in mm3 L−1) predicted for different atmospheric pCO2 levels and lake properties. The lake properties are (A, B) lake depth (zMAX), (C, D) CO2 gas transfer velocity (v), (E, F) DIC concentration of the influx ([DIC]IN), and (G, H) salinity (Sal). The model considers a low-alkaline lake (ALKIN = 0.5 mEq L−1). Vertical lines represent atmospheric CO2 levels of 400 ppm (present-day) and 750 ppm (predicted for the year 2150 by the RCP6 scenario of the IPCC). Horizontal dotted lines represent our default parameter values. In (E, F), the dotted line indicates equilibrium with the atmospheric CO2 pressure. The contour plots are based on steady-state solutions across a grid of 40×50 = 2,000 simulations.
The CO2 gas transfer velocity across the air-water interface varies with wind speed and precipitation events , , . An increase in CO2 gas transfer velocity strongly reduces the level of carbon limitation and increases the phytoplankton population density (Fig. 8C, D). Interestingly, the sensitivity coefficients point at an interactive effect with the atmospheric CO2 level. The model predictions become more sensitive to changes in CO2 gas transfer velocity at higher atmospheric CO2 levels (Table 1).
Enhanced mineralization of organic carbon in the sediment or additional CO2 input from the surrounding watershed may cause an enhanced CO2 influx into the lake. In our model this would be represented by an increase in DIC influx without a change in alkalinity. Such an enhanced CO2 influx reduces the level of carbon limitation, thereby raising phytoplankton population density (Fig. 8E, F). The sensitivity coefficients indicate that the model predictions respond strongly to changes in DIC input (Table 1).
Salinity has a negative impact on the solubility of CO2 in water , but a positive impact on the dissociation constants of carbonic acid and bicarbonate . We explored salinities from 0 to 40 g L−1, covering the full salinity range from freshwater lakes to the oceans. The results show that, all else being equal, changes in salinity have only minor effects on the predicted level of carbon limitation and phytoplankton population density (Fig. 8G, H; Table 1).
All normalized sensitivity coefficients remained below 1, indicating that none of the model parameters had an unexpectedly strong nonlinear effect on the model output.
Coupling between phytoplankton blooms and inorganic carbon chemistry
Our theoretical and experimental results demonstrate that the development of dense algal blooms can dramatically change the dissolved CO2 concentration, alkalinity and pH of aquatic ecosystems. In our experiments, phytoplankton growth induced a strong CO2 drawdown, especially when provided with a low pCO2 level in the gas flow. Assimilation of CO2 and nutrients such as nitrate, phosphate and sulfate increased alkalinity and pH during bloom development –. Increases in pH and alkalinity shifted the inorganic carbon composition towards bicarbonate and carbonate. These findings are in good agreement with field observations, as similar changes in DIC speciation, pH, and alkalinity have also been documented in studies of dense phytoplankton blooms in natural waters (Fig. 1) , , .
Dense phytoplankton blooms contribute to both ‘biological enhancement’ and ‘chemical enhancement’ of the CO2 influx into aquatic ecosystems. Biological enhancement is due to the drawdown of the dissolved CO2 concentration by dense phytoplankton blooms, which enlarges the CO2 concentration gradient across the air-water interface. Hence, dense phytoplankton blooms can turn aquatic ecosystems into net carbon sinks, and the resultant influx of atmospheric CO2 can further fuel phytoplankton growth , . Chemical enhancement occurs because part of the influx of CO2 chemically reacts with water, and is transferred to bicarbonate and carbonate . This chemical enhancement is promoted by the high pH and alkalinity induced by phytoplankton blooms, which enlarge the DIC storage capacity of aquatic ecosystems.
Interestingly, our laboratory experiments show that the enhanced CO2 influx induced by dense phytoplankton populations can even raise the bicarbonate and total DIC concentration (Fig. 2E, 2F, 4G). This may seem counterintuitive, because phytoplankton populations consume inorganic carbon. However, the high pH and alkalinity in phytoplankton blooms favors the formation of bicarbonate and carbonate. Depending on the interplay between CO2 gas transfer, inorganic carbon uptake, alkalinity and pH, this can result in either a decrease or increase in total DIC concentration. The lake model predicts that dense phytoplankton blooms may increase the bicarbonate and DIC concentration in lakes, but only at very high pCO2 levels. At pCO2 levels below 1,400 ppm, the lake model predicts a reduced bicarbonate and DIC concentration during phytoplankton blooms (Fig. 5D, G), which is supported by our observations from Lake Volkerak (Fig. 1B).
In contrast to nutrients and light, carbon availability is often dismissed as an important limiting factor for phytoplankton growth. One common argument is that the CO2 concentrations in many freshwater lakes are sufficiently high to cover the carbon demands of phytoplankton populations, because these lakes are often supersaturated with CO2 , , . However, dense phytoplankton blooms can strip surface waters from dissolved CO2, as has been observed in a wide range of aquatic ecosystems , , . This is exemplified by our data from Lake Volkerak, which is supersaturated with CO2 in winter, yet dense cyanobacterial blooms deplete the CO2 concentration during the summer period (Fig. 1). Our laboratory experiments and model simulations indicate that dense phytoplankton blooms can deplete the dissolved CO2 concentration of low-alkaline waters by two to three orders of magnitude (Figs. 2, 4, 5).
Another common argument is that alkaline lakes typically have sufficiently high bicarbonate concentrations to cover the carbon demands of phytoplankton populations. Indeed, in addition to CO2, many phytoplankton species also utilize bicarbonate as carbon source –. However, utilization of bicarbonate requires additional investments in, e.g., sodium-dependent and ATP-dependent bicarbonate uptake systems and carbonic anhydrases , . The costs of bicarbonate utilization may therefore have repercussions for the growth rates that can be achieved. Synechococcus leopoliensis, for instance, grows at ∼80% of its maximum growth rate when provided with bicarbonate as its main carbon source . Our parameter estimates indicate that Microcystis CYA 140 grows at <50% while Microcystis HUB5-2-4 can only grow at 35% of its maximum growth rate on bicarbonate alone (Table S2.3 in Text S2). This is supported by the chemostat experiments. For instance, Microcystis HUB5-2-4 could just barely sustain a low population density when CO2 was largely removed from the gas flow, even though bicarbonate was provided at a saturating concentration of 2,000 µmol L−1 in the mineral medium (see the datapoint at 0.5 ppm pCO2 in Fig. 4A). For both strains, an increase in pCO2 level led to a clear increase in population density (Figs. 2 and 4). Hence, our experiments demonstrate that, even for cyanobacteria with their sophisticated carbon-concentrating mechanisms, increasing pCO2 levels in bicarbonate-rich waters can cause an increase in phytoplankton population density.
In line with expectation, our model predicts that the potential for carbon limitation strongly depends on alkalinity (Fig. 6). This is consistent with studies in natural waters. Carbon limitation is often observed during algal blooms in eutrophic low-alkaline lakes, where CO2 is the main inorganic carbon source , . Carbon limitation has also been reported for moderately alkaline lakes (Fig. 1) , , , where bicarbonate partially supplements phytoplankton growth when CO2 is depleted. The model predicts that carbon limitation will be almost absent in high-alkaline waters and soda lakes, owing to their high inorganic carbon availability (Fig. 6). Indeed, tropical soda lakes are widely recognized to be among the world’s most productive ecosystems, and can sustain extremely dense populations of cyanobacteria , .
Only high nutrient loads can sustain phytoplankton blooms dense enough to deplete the dissolved CO2 concentration and induce carbon limitation . In an analysis of 131 eutrophic lakes in the Midwestern USA, Balmer and Downing  showed that dissolved CO2 decreased below atmospheric equilibrium when total phosphorus (TP) concentrations exceeded 1–2 µmol L−1 and chlorophyll a levels exceeded 10–20 µg L−1. Severe CO2 depletion occurred at chlorophyll concentrations exceeding 80–100 µg L−1. This matches our data from Lake Volkerak, which has a summer TP concentration of ∼3 µmol L−1 , and where the dissolved CO2 concentration became undersaturated at chlorophyll concentrations exceeding 20 µg L−1 and was severely depleted during the height of the blooms (Fig. 1A). Such conditions also seem to be representative of several other eutrophic and hypertrophic lakes with dense phytoplankton blooms. For example, TP concentrations exceeding 2 µmol L−1 are also found in Lake Taihu in China , Lake Victoria in East Africa , the western part of Lake Erie, USA , , the southern part of Lake Peipsi on the border of Estonia and Russia , , and several smaller lakes and reservoirs , , , all of which have suffered from dense cyanobacterial blooms in summer. This indicates that the nutrient availability in these eutrophic and hypertrophic lakes is, at least in potential, high enough for dense phytoplankton blooms to induce carbon-limited conditions.
Combining models and experiments has several advantages. It allows quantitative analysis of the different processes under controlled conditions. Furthermore, it ensures that model predictions are strongly grounded in measured data, which adds confidence to the model output. Moreover, the model aids interpretation of the experimental results, and also offers a tool for extrapolation of the investigated processes to natural waters (Figs. 4–7).
Nevertheless, like all models, our model is at best a major simplification of reality, based on a series of simplifying assumptions that ignore many of the intriguing complexities of the natural world. In particular, the domain of applicability of our model predictions is restricted to eutrophic and hypertrophic waters where all nutrients are in excess. In oligotrophic waters, rising atmospheric CO2 levels will probably have a much smaller effect on the development of phytoplankton blooms, because nutrient limitation suppresses phytoplankton growth , . Therefore, we recently extended our model and associated experiments to nutrient-limited conditions . This confirmed that, at low nutrient levels, rising CO2 concentrations will have much less impact on phytoplankton biomass development. Lower phytoplankton population densities will lead to less CO2 depletion and have a smaller impact on pH. However, at low nutrient levels, rising CO2 concentrations may lead to a strong increase of the carbon:nutrient stoichiometry of phytoplankton, with possible repercussions for their nutritional quality as food for herbivores .
Furthermore, natural waters vary in phytoplankton species composition, while our laboratory experiments were based on a single species only. Cyanobacteria and eukaryotic phytoplankton show genetic and physiological variation in carbon concentrating mechanisms, both between and within species –. Likewise, lakes vary in lake depth and DIC input from the surrounding watershed. We therefore performed a sensitivity analysis to assess how intrinsic uncertainty and natural variation in the model parameters would affect the model predictions. The sensitivity analysis shows that the model predictions are relatively robust to variation in species traits such as the half-saturation constants of CO2 and bicarbonate uptake, but respond strongly to changes in lake depth, CO2 gas transfer velocity and DIC input. The sensitivity of the model predictions to these lake properties indicates that the response to rising CO2 levels is likely to be lake specific. Yet, the general patterns predicted by the model are qualitatively robust, in the sense that rising atmospheric CO2 levels are predicted to alleviate the level of carbon limitation and to increase phytoplankton population densities irrespective of the exact parameter values used (Figs. 7, 8).
Finally, we emphasize that the extrapolation of our model to natural waters is intended to be of an exploratory nature. We focused exclusively on feedbacks between dense phytoplankton blooms and the inorganic carbon chemistry of lakes. However, many other processes are also known to affect phytoplankton blooms, such as nutrient availability, thermal stratification, and day-to-day weather variability , , . Interactions with other species in the food web may induce phytoplankton-zooplankton oscillations , , the collapse of phytoplankton blooms by viruses , and other nonequilibrium dynamics . Furthermore, the alkalinity and pH of natural systems is influenced not only by phytoplankton growth, but also by a variety of hydrological and biogeochemical processes , , . Application of our model to specific phytoplankton blooms in specific lakes is encouraged, but will require incorporation of the myriad of additional processes that are considered to be of relevance for the particular lake under study.
Effects of rising CO2
Our results support earlier reports that rising atmospheric pCO2 levels are likely to promote phytoplankton productivity in eutrophic waters , . More specifically, both our model predictions and laboratory experiments indicate that elevation of the atmospheric pCO2 will enhance the CO2 influx across the air-water interface during dense phytoplankton blooms, which in turn will tend to further increase the population density of these blooms.
Our study shows that dense phytoplankton blooms are capable to deplete the dissolved CO2 concentration and increase the pH over a relatively wide range of atmospheric CO2 levels (Fig. 4C, E, Fig. 5C, E). Yet, at some point, rising atmospheric CO2 levels will alleviate phytoplankton blooms from carbon limitation, such that they will exert much less control over the dissolved CO2 concentration and pH. Beyond this point, phytoplankton blooms become carbon-saturated and a further rise in atmospheric CO2 levels will not enhance population densities but will lead to less intense CO2 depletion and a lower pH during the blooms. Our results indicate that the atmospheric CO2 level at which blooms become carbon-saturated is likely to vary among phytoplankton species depending on e.g. their carbon concentrating mechanisms –, and among ecosystems depending on e.g. alkalinity, lake depth and CO2 input from the mineralization of dissolved organic carbon (Figs. 6–8). For instance, in our chemostat experiments the population density increased for atmospheric pCO2 levels from 10 to 200 ppm, while the Microcystis population became carbon-saturated at pCO2 levels beyond 200 ppm (Fig. 4A). In contrast, for low-alkaline lakes, our baseline model predicts a strong increase in phytoplankton population density from 100 to 1,500 ppm, while the transition to carbon-saturated Microcystis blooms is predicted to occur only when the pCO2 level exceeds 1,500 ppm (Fig. 5A).
Intensification of phytoplankton blooms by rising CO2 levels may further aggravate the problems associated with these blooms, such as anoxia and fish kills ,  and the loss of submerged vegetation due to an increased turbidity , . In particular, enhanced bloom formation by toxic phytoplankton species, like the cyanobacterium Microcystis of this study, can pose health risks for humans and animals, and may threaten the use of eutrophic waters for recreation, fisheries, drinking water and agricultural irrigation –.
The interplay between data-driven models and model-driven experimentation explored by our study may offer an important step towards an improved quantitative understanding and prediction of the impacts of rising CO2 on phytoplankton blooms. Our results demonstrate that, under controlled laboratory conditions, the coupling between phytoplankton growth, CO2 drawdown and the inorganic carbon chemistry of aquatic systems can be captured by a relatively simple model. Extrapolation of this experimentally validated model to lakes warns that rising CO2 levels are likely to intensify phytoplankton blooms, especially in low to moderately alkaline waters with high nutrient loads.
Sampling of Lake Volkerak. Description of the lake, sampling method and analysis of the data displayed in Fig. 1.
Model description and parameter estimation. Full description of the model used to predict the population dynamics, inorganic carbon chemistry, pH and alkalinity in the chemostat. Solubility and dissociation constants of dissolved inorganic carbon and phosphate are given in Table S2.1 in this text. System parameters and phytoplankton parameters are listed in Tables S2.2 and S2.3, respectively.
Adaptation of the model to lakes. Detailed description of the extended model formulation to apply the model to lakes.
Dynamic changes in inorganic carbon chemistry and pH without phytoplankton. Auxiliary experiments investigating dynamic changes in inorganic carbon chemistry and pH in six chemostats without phytoplankton. The experimental data and model fits are displayed in Fig. S4.1, and the estimated parameter values are given in Table S4.1 in this text.
We thank Hans G. Dam and the four anonymous reviewers for their constructive comments on the manuscript, Virgilio Floris, Roel Pel and Hans Hoogveld, for analysis of DIC data of Lake Volkerak, and Leo Hoitinga and Bert de Leeuw for their contribution to the nutrient analyses.
Conceived and designed the experiments: JMHV DBVDW PMV EVD JH. Performed the experiments: JMHV DBVDW JFF. Analyzed the data: JMHV DBVDW JH. Contributed reagents/materials/analysis tools: EVD JH. Wrote the paper: JMHV DBVDW JH. Designed the model: JMHV JH.
- 1. Stocker TF, Qin D, Plattner GK, Tignor M, Allen SK, et al. (2013) Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, 1535 p.
- 2. Orr JC, Fabry VJ, Aumont O, Bopp L, Doney SC, et al. (2005) Anthropogenic ocean acidification over the twenty-first century and its impact on calcifying organisms. Nature 437: 681–686.
- 3. Doney SC, Fabry VJ, Feely RA, Kleypass JA (2009) Ocean acidification: the other CO2 problem. Ann Rev Mar Sci 1: 169–192.
- 4. Del Giorgio PA, Peters RH (1994) Patterns in planktonic P:R ratios in lakes: influence of lake trophy and dissolved organic carbon. Limnol Oceanogr 39: 772–787.
- 5. Cole JJ, Caraco NF, Kling GW, Kratz TK (1994) Carbon dioxide supersaturation in the surface waters of lakes. Science 265: 1568–1570.
- 6. Sobek S, Tranvik LJ, Cole JJ (2005) Temperature independence of carbon dioxide supersaturation in global lakes. Global Biogeochem Cycles 19: GB2003 doi:10.1029/2004GB002264.
- 7. Lazzarino JK, Bachmann RW, Hoyer MV, Canfield Jr DE (2009) Carbon dioxide supersaturation in Florida lakes. Hydrobiologia 627: 169–180.
- 8. Giordano M, Beardall J, Raven JA (2005) CO2 concentrating mechanisms in algae: mechanisms, environmental modulation, and evolution. Ann Rev Plant Biol 56: 99–131.
- 9. Price GD, Badger MR, Woodger FJ, Long BM (2008) Advances in understanding the cyanobacterial CO2-concentrating-mechanism (CCM): functional components, Ci transporters, diversity, genetic regulation and prospects for engineering into plants. J Exp Bot 59: 1441–1461.
- 10. Sandrini G, Matthijs HCP, Verspagen JMH, Muyzer G, Huisman J (2014) Genetic diversity of inorganic carbon uptake systems causes variation in CO2 response of the cyanobacterium Microcystis. ISME J 8: 589–600.
- 11. Talling JF (1976) The depletion of carbon dioxide from lake water by phytoplankton. J Ecol 64: 79–121.
- 12. Maberly SC (1996) Diel, episodic and seasonal changes in pH and concentrations of inorganic carbon in a productive lake. Freshw Biol 35: 579–598.
- 13. Hein M (1997) Inorganic carbon limitation of photosynthesis in lake phytoplankton. Freshw Biol 37: 545–552.
- 14. Gu B, Schelske CL, Coveney MF (2011) Low carbon dioxide partial pressure in a productive subtropical lake. Aquat Sci 73: 317–330.
- 15. Balmer MB, Downing JA (2011) Carbon dioxide concentrations in eutrophic lakes: undersaturation implies atmospheric uptake. Inland Waters 1: 125–132.
- 16. Ibelings BW, Maberly SC (1998) Photoinhibition and the availability of inorganic carbon restrict photosynthesis by surface blooms of cyanobacteria. Limnol Oceanogr 43: 408–419.
- 17. Verschoor AM, Van Dijk MA, Huisman J, Van Donk E (2013) Elevated CO2 concentrations affect the elemental stoichiometry and species composition of an experimental phytoplankton community. Freshw Biol 58: 597–611.
- 18. López-Archilla A, Moreira D, López-García P, Guerrero C (2004) Phytoplankton diversity and cyanobacterial dominance in a hypereutrophic shallow lake with biologically produced alkaline pH. Extremophiles 8: 109–115.
- 19. Shapiro J (1997) The role of carbon dioxide in the initiation and maintenance of blue-green dominance in lakes. Freshw Biol 37: 307–323.
- 20. Caraco NF, Miller R (1998) Effects of CO2 on competition between a cyanobacterium and eukaryotic phytoplankton. Can J Fish Aquat Sci 55: 54–62.
- 21. Chorus I, Bartram J, eds. (1999) Toxic Cyanobacteria in Water: A Guide to their Public Health Consequences, Monitoring and Management. Spon, London. 416 p.
- 22. Huisman J, Matthijs HCP, Visser PM, eds. (2005) Harmful Cyanobacteria. Springer, Berlin. 241 p.
- 23. Michalak AM, Anderson EJ, Beletsky D, Boland S, Bosche NS, et al. (2013) Record-setting algal bloom in Lake Erie caused by agricultural and meteorological trends consistent with expected future conditions. Proc Natl Acad Sci USA 110: 6448–6452.
- 24. Guo L (2007) Doing battle with the green monster of Taihu Lake. Science 317: 1166.
- 25. Xu H, Paerl HW, Qin B, Zhu G, Gao G (2010) Nitrogen and phosphorus inputs control phytoplankton growth in eutrophic Lake Taihu, China. Limnol Oceanogr 55: 420–432.
- 26. Ozawa K, Fujioka H, Muranaka M, Yokoyama A, Katagami Y, et al. (2005) Spatial distribution and temporal variation of Microcystis species composition and microcystin concentration in Lake Biwa. Environ Toxicol 20: 270–276.
- 27. Ochumba PBO, Kibaara DI (1989) Observations on blue-green algal blooms in the open waters of Lake Victoria, Kenya. Afr J Ecol 27: 23–34.
- 28. Verschuren D, Johnson TC, Kling HJ, Edgington DN, Leavitt PR, et al. (2002) History and timing of human impact on Lake Victoria, East Africa. Proc R Soc Lond B 269: 289–294.
- 29. Kanoshina I, Lips U, Leppänen JM (2003) The influence of weather conditions (temperature and wind) on cyanobacterial bloom development in the Gulf of Finland (Baltic Sea). Harmful Algae 2: 29–41.
- 30. Suikkanen S, Laamanen M, Huttunen M (2007) Long-term changes in summer phytoplankton communities of the open northern Baltic Sea. Estuar Coast Shelf Sci 71: 580–592.
- 31. Verspagen JMH, Passarge J, Jöhnk KD, Visser PM, Peperzak L, et al. (2006) Water management strategies against toxic Microcystis blooms in the Dutch delta. Ecol Appl 16: 313–327.
- 32. Beaulieu M, Pick F, Gregory-Eaves I (2013) Nutrients and water temperature are significant predictors of cyanobacterial biomass in a 1147 lakes data set. Limnol Oceanogr 58: 1736–1746.
- 33. Jöhnk KD, Huisman J, Sharples J, Sommeijer B, Visser PM, et al. (2008) Summer heatwaves promote blooms of harmful cyanobacteria. Glob Chang Biol 14: 495–512.
- 34. Paerl HW, Huisman J (2008) Blooms like it hot. Science 320: 57–58.
- 35. O’Neil JM, Davis TW, Burford MA, Gobler CJ (2012) The rise of harmful cyanobacteria blooms: The potential roles of eutrophication and climate change. Harmful Algae 14: 313–334.
- 36. Verspagen JMH, Snelder EOFM, Visser PM, Jöhnk KD, Ibelings BW, et al. (2005) Benthic-pelagic coupling in the population dynamics of the harmful cyanobacterium Microcystis. Freshw Biol 50: 854–867.
- 37. Huisman J, Sharples J, Stroom JM, Visser PM, Kardinaal WEA, et al. (2004) Changes in turbulent mixing shift competition for light between phytoplankton species. Ecology 85: 2960–2970.
- 38. Goldman JC, Brewer PG (1980) Effect of nitrogen source and growth rate on phytoplankton-mediated changes in alkalinity. Limnol Oceanogr 25: 352–357.
- 39. Schindler DW, Turner MA, Hesslein RH (1985) Acidification and alkalinization of lakes by experimental addition of nitrogen compounds. Biogeochemistry 1: 117–133.
- 40. Wolf-Gladrow DA, Zeebe RE, Klaas C, Körtzinger A, Dickson AG (2007) Total alkalinity: the explicit conservative expression and its application to biogeochemical processes. Mar Chem 106: 287–300.
- 41. Portielje R, Lijklema L (1995) Carbon dioxide fluxes across the air-water interface and its impact on carbon availability in aquatic systems. Limnol Oceanogr 40: 690–699.
- 42. Stumm W, Morgan JJ (1996) Aquatic Chemistry: Chemical Equilibria and Rates in Natural Waters. New York: Wiley-Interscience. 1022pp.
- 43. Lewis E, Wallace DWR (1998) Program developed for CO2 system calculations. Oak Ridge: Carbon Dioxide Information Analysis Center, rep. ORNL/CDIAC-105, Oak Ridge Natl Lab, US Dept of Energy. 21 p.
- 44. Droop MR (1973) Some thoughts on nutrient limitation in algae. J Phycol 9: 264–272.
- 45. Grover JP (1991) Resource competition in a variable environment: phytoplankton growing according to the variable-internal-stores model. Am Nat 138: 811–835.
- 46. Huisman J, Weissing FJ (1994) Light-limited growth and competition for light in well-mixed aquatic environments: an elementary model. Ecology 75: 507–520.
- 47. Diehl S (2002) Phytoplankton, light, and nutrients in a gradient of mixing depths: theory. Ecology 83: 386–398.
- 48. Klausmeier CA, Litchman E, Levin SA (2004) Phytoplankton growth and stoichiometry under multiple nutrient limitation. Limnol Oceanogr 49: 1463–1470.
- 49. Passarge J, Hol S, Escher M, Huisman J (2006) Competition for nutrients and light: stable coexistence, alternative stable states, or competitive exclusion? Ecol Monogr 76: 57–72.
- 50. Morel FMM (1987) Kinetics of nutrient uptake and growth in phytoplankton. J Phycol 23: 137–150.
- 51. Huisman J (1999) Population dynamics of light-limited phytoplankton: microcosm experiments. Ecology 80: 202–210.
- 52. Visser PM, Passarge J, Mur LR (1997) Modelling vertical migration of the cyanobacterium Microcystis. Hydrobiologia 349: 99–109.
- 53. Siegenthaler U, Sarmiento JL (1993) Atmospheric carbon dioxide and the ocean. Nature 365: 119–125.
- 54. Cole JJ, Caraco NF (1998) Atmospheric exchange of carbon dioxide in a low-wind oligotrophic lake measured by the addition of SF6. Limnol Oceanogr 43: 647–656.
- 55. Huisman J, Jonker RR, Zonneveld C, Weissing FJ (1999) Competition for light between phytoplankton species: experimental tests of mechanistic theory. Ecology 80: 211–222.
- 56. Van de Waal DB, Verspagen JMH, Finke JF, Vournazou V, Immers AK, et al. (2011) Reversal in competitive dominance of a toxic versus non-toxic cyanobacterium in response to rising CO2. ISME J 5: 1438–1450.
- 57. Van de Waal DB, Verspagen JMH, Lürling M, Van Donk E, Visser PM, et al. (2009) The ecological stoichiometry of toxins produced by harmful cyanobacteria: an experimental test of the carbon-nutrient balance hypothesis. Ecol Lett 12: 1326–1335.
- 58. Diehl S, Berger S, Ptacnik R, Wild A (2002) Phytoplankton, light, and nutrients in a gradient of mixing depths: field experiments. Ecology 83: 399–411.
- 59. Murphy J, Riley JP (1962) A modified single-solution method for the determination of phosphate in natural waters. Water Sci Technol 32: 25–34.
- 60. Wetzel RG, Likens GE (2000) Limnological Analysis. New York: Springer-Verlag. 429pp.
- 61. Crusius J, Wanninkhof R (2003) Gas transfer velocities measured at low wind speed over a lake. Limnol Oceanogr 48: 1010–1017.
- 62. Guérin F, Abril G, Serça D, Delon C, Richard S, et al. (2007) Gas transfer velocities of CO2 and CH4 in a tropical reservoir and its river downstream. J Mar Syst 66: 161–172.
- 63. Saltelli A, Annoni P (2010) How to avoid a perfunctory sensitivity analysis. Environ Modell Softw 25: 1508–1517.
- 64. Frey HC, Patil SR (2002) Identification and review of sensitivity analysis methods. Risk Analysis 22: 553–578.
- 65. Weiss RF (1974) Carbon dioxide in water and seawater: the solubility of a non-ideal gas. Mar Chem 2: 203–215.
- 66. Millero FJ, Graham TB, Huang F, Bustos-Serrano H, Pierrot D (2006) Dissociation constants of carbonic acid in seawater as a function of salinity and temperature. Mar Chem 100: 80–94.
- 67. Schindler DW, Brunskill GT, Emerson S, Broecker WS, Peng TH (1972) Atmospheric carbon dioxide: its role in maintaining phytoplankton standing crops. Science 177: 1192–1194.
- 68. Emerson S (1975) Chemically enhanced CO2 gas exchange in a eutrophic lake: a general model. Limnol Oceanogr 20: 743–753.
- 69. Jansson M, Karlsson J, Jonsson A (2012) Carbon dioxide supersaturation promotes primary production in lakes. Ecol Lett 15: 527–532.
- 70. Miller AG, Turpin DH, Canvin DT (1984) Growth and photosynthesis of the cyanobacterium Synechococcus leopoliensis in HCO3– limited chemostats. Plant Physiol 75: 1064–1070.
- 71. Gu B, Chapman AD, Schelske CL (2006) Factors controlling seasonal variations in stable isotope composition of particulate organic matter in a soft water eutrophic lake. Limnol Oceanogr 51: 2837–2848.
- 72. Berman-Frank I, Zohary T, Erez J, Dubinsky Z (1994) CO2 availability, carbonic anhydrase, and the annual dinoflagellate bloom in Lake Kinneret. Limnol Oceanogr 39: 1822–1834.
- 73. Talling JF, Wood RB, Prosser MV, Baxter RM (1973) The upper limit of photosynthetic productivity by phytoplankton: evidence from Ethiopian soda lakes. Freshw Biol 3: 53–76.
- 74. Oduor SO, Schagerl M (2007) Phytoplankton primary productivity characteristics in response to photosynthetically active radiation in three Kenyan Rift Valley saline-alkaline lakes. J Plankton Res 29: 1041–1050.
- 75. Verspagen JMH, Van de Waal DB, Finke JF, Visser PM, Huisman J (2014) Contrasting effects of rising CO2 on primary production and ecological stoichiometry at different nutrient levels. Ecol Lett 17: 951–960.
- 76. Guildford SJ, Hecky RE (2000) Total nitrogen, total phosphorus, and nutrient limitation in lakes and oceans: is there a common relationship? Limnol Oceanogr 45: 1213–1223.
- 77. Chaffin JD, Bridgeman TB, Heckathorn SA, Mishra S (2011) Assessment of Microcystis growth rate potential and nutrient status across a trophic gradient in western Lake Erie. J Great Lakes Res 37: 92–100.
- 78. Kangur K, Möls T (2008) Changes in spatial distribution of phosphorus and nitrogen in the large north-temperate lowland Lake Peipsi (Estonia/Russia). Hydrobiol 599: 31–39.
- 79. Nõges T, Tuvikene L, Nõges P (2010) Contemporary trends of temperature, nutrient loading, and water quality in large Lakes Peipsi and Võrtsjärv, Estonia. Aquat Ecosyst Health Manag 13: 143–153.
- 80. Sabart M, Pobel M, Briand E, Combourieu B, Salençon MJ, et al. (2010) Spatiotemporal variations in microcystin concentrations and in the proportions of microcystin-producing cells in several Microcystis aeruginosa populations. Appl Environ Microbiol 76: 4750–4759.
- 81. Dzialowski AR, Wang SH, Lim NC, Spotts WW, Huggins DG (2005) Nutrient limitation of phytoplankton growth in central plains reservoirs, USA. J Plankton Res 27: 587–595.
- 82. Anderson DM, Glibert PM, Burkholder JM (2002) Harmful algal blooms and eutrophication: nutrient sources, composition, and consequences. Estuaries 25: 704–726.
- 83. Gulati RD, van Donk E (2002) Lakes in the Netherlands, their origin, eutrophication and restoration: state-of-the-art review. Hydrobiologia 478: 73–106.
- 84. Scheffer M (1998) Ecology of Shallow Lakes. Chapman and Hall, London. 357 p.
- 85. Fussmann GF, Ellner SP, Shertzer KW, Hairston Jr NG (2000) Crossing the Hopf bifurcation in a live predator-prey system. Science 290: 1358–1360.
- 86. Van Hannen EJ, Zwart G, van Agterveld MP, Gons HJ, Ebert J, et al. (1999) Changes in bacterial and eukaryotic community structure after mass lysis of filamentous cyanobacteria associated with viruses. Appl Environ Microbiol 65: 795–801.
- 87. Benincà E, Huisman J, Heerkloss R, Jöhnk KD, Branco P, et al. (2008) Chaos in a long-term experiment with a plankton community. Nature 451: 822–825.
- 88. Soetaert K, Hofmann AF, Middelburg JJ, Meysman FJR, Greenwood J (2007) The effect of biogeochemical processes on pH. Mar Chem 105: 30–51.
- 89. Schippers P, Lürling M, Scheffer M (2004) Increase of atmospheric CO2 promotes phytoplankton productivity. Ecol Lett 7: 446–451.
- 90. Qiu B, Gao K (2002) Effects of CO2 enrichment on the bloom-forming cyanobacterium Microcystis aeruginosa (Cyanophyceae): Physiological responses and relationships with the availability of dissolved inorganic carbon. J Phycol 38: 721–729.
- 91. Hallegraeff GM (1993) A review of harmful algal blooms and their apparent global increase. Phycologia 32: 79–99.