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Article

Nutrient Control to Prevent the Occurrence of Cyanobacterial Blooms in a Eutrophic Lake in Southern Sweden, Used for Drinking Water Supply

1
Department of Building and Environmental Technology/Water Resources Engineering, Lund University, PO Box 118, SE-221 00 Lund, Sweden
2
Department of Biology/Aquatic ecology, Lund University, Sölvegatan 37, SE-223 62 Lund, Sweden
3
Sweden Water Research AB, Ideon Science Park, SE-223 70 Lund, Sweden
*
Author to whom correspondence should be addressed.
Water 2018, 10(7), 919; https://doi.org/10.3390/w10070919
Submission received: 24 April 2018 / Revised: 26 June 2018 / Accepted: 27 June 2018 / Published: 11 July 2018
(This article belongs to the Special Issue Eutrophication Management: Monitoring and Control)

Abstract

:
Control of nutrients, mainly nitrogen (N) and phosphorus (P), plays a significant role in preventing cyanobacterial blooms (harmful algal blooms (HABs)). This study aims at evaluating changes in the risk of the occurrence of cyanobacterial blooms and advancing the understanding of how nitrogen and phosphorus affect the growth of cyanobacteria in a eutrophic lake, Lake Vombsjön, in southern Sweden. Our results show that TP (total phosphorus) has stronger positive correlation with cyanobacteria biomass than DIP (dissolved inorganic phosphorus); DIN (dissolved inorganic nitrogen) has a stronger negative correlation with cyanobacteria biomass than TN (total nitrogen); and DIN:TP has a stronger negative correlation with cyanobacteria biomass than TN:TP. The highest amount of cyanobacteria biomass, above WHO (World Health Organization) Alert Level 2 (10 mm3/L) for drinking water correspond to the DIN/TP ratio below 10. To diminish the growth of cyanobacteria in Lake Vombsjön, TP and DIN control should be in focus, preferably a TP below 20 µg/L, and the DIN:TP ratio should be maintained at a level of at least above 10, but preferably above 50, thereby reducing the likelihood for a nitrogen limiting situation which may favor cyanobacteria dominating blooms.

Graphical Abstract

1. Introduction

Harmful algal blooms (HABs), specifically those caused by cyanobacteria, have become one of the most critical concerns for drinking water supply, as well as for maintaining the ecological and economic sustainability of freshwater ecosystems worldwide [1,2]. Eutrophication is the major process stimulating the growth of algal and cyanobacterial biomass, the key factors here being the maintaining of a high availability of important nutrients, such as phosphorus (P) and nitrogen (N), and also a low N/P ratio [3,4]. Cyanobacterial blooms are predicted to become even more common due to climate warming [2,5]. Recent studies have also demonstrated that synergies between climate warming and increasing levels of humic substances in runoff are able to trigger an increase in cyanobacteria biomass [6], as well as a reduction in the biodiversity of phytoplankton [7,8]. Accordingly, both global and local scale adaptive management tools are important to manage future challenges related to water security and adequate functioning of freshwater ecosystems [7].
Regarding drinking water supply, major reasons for the strong impact of cyanobacterial blooms are that large algal blooms tend to clog the treatment process. They also cause unpleasant smells, may produce toxins [7,8,9], and are difficult to remove [10]. There is even a cyanotoxin risk in the sludge managed at drinking water treatment plants [11]. Nearly all eutrophic freshwater bodies contain toxic cyanobacteria though the size of cyanobacterial populations may also be dependent upon such environmental conditions, temperature, mixing regimes, transparency, and the availability of iron or carbon [12,13,14,15].
Hence, to meet future challenges with respect to ecosystem services, such as the provision of clean drinking water, it is crucial to reduce the input of nutrients to aquatic ecosystems [16,17,18]. Phosphorus is commonly considered to be the limiting nutrient in freshwater ecosystems [19], and high concentrations of P often co-occur with severe cyanobacterial blooms in many regions of the world, such as in large lakes in North America and in China [20,21]. To reduce the probability that the biomass of HABs reach concentrations above WHO Alert Level 1 (0.2 mm3/L) for drinking waters [1] in Swedish lakes, it has been recommended to reduce TP (total phosphorus) below 20 μg/L in this particular region and climate [22].
Although phosphorus is generally the main limiting nutrient for cyanobacterial growth in freshwaters, nitrogen may sometimes be co-limiting, since it is a quantitatively important bio-element [23]. However, contrary to most other planktonic algae, some cyanobacteria are able to fix atmospheric nitrogen in a nitrogen-limiting situation, which can lead to a lack of nitrates or of ammonia, and in turn to a dominance of N2-fixing cyanobacteria such as Anabaena spp. and Aphanizomenon spp. [24]. For instance, the drop of dissolved inorganic nitrogen (DIN) correlated with an increase of N2 fixation rates and Aphanizomenon abundance in the eutrophic Lake Mendota, Wisconsin, USA [25]. Another example is that under nitrogen-limiting conditions the abundance of various common toxic cyanobacteria, such as Microcystis aeruginosa, which are not capable of fixing N2, declines, whereas their biomass increases again as nitrogen becomes more readily available [26]. Because of differences in the N2 fixation capabilities involved, many studies have examined interactions between cyanobacterial blooms and the nutrients available to them. For example, in Lake Taihu, China, the availability of P has been found to control the pre-bloom conditions of Microcystis spp. during the spring months, whereas the availability of N controls the blooms of this species during the summer months. The thresholds for the limitations of TN and TP were estimated to below 800 μg/L and below 50 μg/L, respectively [16].
In addition to the absolute concentrations of the nutrients, the ratio of nitrogen to phosphorus (the N:P ratio) has been considered to be one of the main parameters in determining cyanobacterial growth [4,5,27]. Keeping the absolute concentrations of N and P at low levels and combined with this, maintaining a high TN:TP ratio above 30, reduces the risk of cyanobacterial blooms [28]. A high concentration of P and a low N:P ratio tend to favour the development of cyanobacterial blooms [29], since for some species, nitrogen deficits may be compensated by nitrogen fixation from the atmosphere. However, a low N:P ratio does not always lead to a nitrogen limiting situations and nitrogen fixation conditions, since it is also affected by the phytoplankton biomass and by the nitrogen concentration [4]. Hence, a low N:P ratio alone does not suffice for appreciably limiting the development of cyanobacterial blooms. In this study, we thus compared the influence of DIN, DIP (dissolved inorganic phosphorus), TP, TN, TN:TP, and DIN:TP on cyanobacteria biomass separately and tested if DIN:TP was a better indicator of cyanobacteria peaks.
From both a research and a management perspective, it is highly important to identify and control environmental processes that have the potential of driving and sustaining cyanobacterial blooms [30]. Beside nutrient reduction, there are many factors influencing ecosystem function, such as shifting baselines where changes in forcing factors other than nutrients, such as climate and food web structure. Understanding how ecosystems respond to multiple shifting baselines is essential in order to set reliable targets for restoration efforts [31]. For a successful monitoring of ecosystem transitions, a priori specific knowledge of the underlying processes/mechanisms driving ecosystem transitions is required [32]. The more eutrophic a lake is, the more sensitive cyanobacteria will be to the interactions between nutrients and temperature, but ultimately the nutrient level is the more important predictor for cyanobacterial biomass development [33]. To reduce cyanobacteria growth, we need system-specific analytic and management approaches of different kinds, which define the combined monitoring of nutrient concentrations, cyanobacteria and cyanotoxin concentrations [22].
To obtain a better understanding on how nutrient concentrations and nutrient ratios affect the frequency and intensity of cyanobacterial blooms and the ecosystem services provided by lakes, long-term data for Lake Vombsjön, in southern Sweden, which serves as a raw water resource for more than 500,000 inhabitants, were collected and evaluated. We examined seasonal, as well as long-term trends in nutrient levels, in N:P and DIN:TP ratios, in phytoplankton species compositions and in their interactions. The rationale for the study was to use a model lake, Lake Vombsjön, to obtain a detailed understanding of the formation of harmful cyanobacterial blooms, which could serve as a basis for a general understanding of efficient management of eutrophic lakes.
We employed system analysis and statistical analysis to identify the critical nutrient drivers of harmful algal blooms and seasonal patterns of phytoplankton dominance. By using a long-term time series from a eutrophic lake in southern Sweden as model system, we specifically tested the hypothesis that DIN/TP might be a better precursor, and even an early warning signal [32] for cyanobacterial blooms.

2. Materials and Methods

Lake Vombsjön is part of Kävlingeån River’s catchment area (See Figure S1). It is situated 20 km east of the city of Lund. The main type of land use within the catchment area are agriculture (72%) and forestry (23%), whereas urban living areas (3%) and lakes (2%) cover only a minor portion of the area. The lake has a surface area of approximately 12 km2 and the average and a maximum depths of 9.4 and 16.0 m, respectively [34]. The lake has a turnover time of 1.04 years. The main inflow to the lake is that from the Björkaån River (76%). Some 20% of the water flow (of 31 Mm3/year) from Lake Vombsjön is used for drinking water.
Due to Lake Vombsjön being located in what is both an agricultural and a highly populated region, the water quality of the lake suffers considerably from the leaching of nutrients and pesticides from the wastewater and agriculture. More than 85% of the external phosphorus and nitrogen load is from agricultural activities [35]. The accumulation of large amounts of nutrients in the lake sediments has also become a challenge for nutrient management of the lake.
Data on nutrients in the outlet from Lake Vombsjön was collected from 1990 to 2016 within the framework of the regional and national environmental water recipient monitoring program (Vattenanknuten recipientkontrollprogram [36]), led by the Kävlingeåns Water Protection Agency [37]. Data was analyzed by ALcontrol AB, methods for TP µg/L: SS-EN ISO 156812:2005, TN µg/L: SS-EN ISO 12260:2004, NOx-N µg/L: ISO 15923-12013 C, NH4-N µg/L: ISO 15923-12013 B, PO4-P µg/L: SS-EN ISO 6878:2005 [38]. Dissolved inorganic nitrogen (DIN) is the sum of NOx-N and NH4-N.
Phytoplankton data from 1989 to 2010 was provided by the county board of Scania and was analyzed using the method of Utermöhl for quantitative assessment of phytoplankton [39]. Data for 2016 was provided by Sydvatten AB, one of the largest water suppliers in southern Sweden. Samples were taken of the incoming water to the drinking water treatment plant in the area (the Vomb water treatment plant) [40].
To assess the relationship between nutrients and phytoplankton data, we used the non-parametric Spearman’s rank correlation coefficient. The Spearman’s correlation between two variables will be high when the observations have a similar rank (or identical for a correlation of 1) and low when the observations have a dissimilar (or completely opposite for a correlation of −1) rank. p-Value is the significant level which shows the likelihood that the two variables are uncorrelated [41]. Boxplots were used to visualize the seasonal pattern of cyanobacteria and the variation of its percentage in the phytoplankton community.

3. Results and Discussion

3.1. Nutrient Condition at Lake Vombsjön

Temporal nutrient trends in the main inflow to Lake Vombsjön, the Björkaån River, have shown an increasing tendency during recent decades (See Figure S2a). In contrast, there has been a decreasing trend in both TN and TP concentrations at the main outlet from Lake Vombsjön, although the levels have remained high with average concentrations of around 1000 µg/L and 55 µg/L, respectively (See Figure S2b). Thus, very large amounts of nutrients have remained in the lake, as can be seen as in See Figure S2c, which also demonstrates a considerable potential for nutrients to accumulate in the lake. For the period reported in this study, phosphorus deposition in the lake sediments was below 1 ton per year. This translates to an internal P load of which approximately 38% (corresponding to 226 tons) involves three P fractions, which are not stable but instead can readily be released into the water [42]. The TN load has reached about 914 tons per year, 96% of which is from diffuse sources, specifically from agriculture, forests, and pasture lands [43]. The large amounts of nutrients provide a considerable opportunity for algae to grow. In a Swedish national research project, entitled WATERS, aimed at obtaining a dataset for the ecological assessment of Swedish water bodies, it was found that levels of TP > 20 µg/L or of TN > 500 µg/L were indicative of a heightened risk of health-related problems connected with cyanobacteria [44]. In line with this, it may be concluded that Lake Vombsjön is not in a healthy state since TP levels are about two times higher, and TN levels about four times higher than the recommended thresholds.

3.2. Seasonal Pattern of Cyanobacteria

Heavy algal blooms have been observed in Lake Vombsjön almost every summer since the 1970s. There is a clear seasonal pattern in the cyanobacterial development, which often starts with an initial bloom in spring, followed by an increase during July and August, which generally peaks in September and then eventually declines (Figure 1a). In July, the median values of cyanobacteria biomass generally exceed the WHO alert level 1, 0.2 mm3/L for drinking waters (blue line in Figure 1a) [1]. More than 80% of the samples obtained during the past 26 years have been above alert level 1 and 13% have been above the WHO Alert level 2, (10 mm3/L) for drinking waters. The Finnish National Supervisory Authority for Welfare and Health has chosen 0.1 mm3/L as national alert level 1 for operators of drinking water treatment plants to increase raw water monitoring and 1 mm3/L for actions to be initiated, such as risk assessment and information to authorities [45]. Since in general 50–75% of algal blooms are toxic [46], this suggests that raw water taken from the lake for drinking water purposes might frequently be toxic during bloom seasons. We also found that the later in the season a bloom occurs, the more likely it is dominated by cyanobacteria (Figure 1b). During the period of September to November the percentage of cyanobacteria present in the phytoplankton community was often above 80% (Figure 1b), suggesting that monitoring of algal blooms in late autumn is crucial.

3.3. Nutrients Influence on Cyanobacteria

As Lake Vombsjön is rich in nutrients, it provides suitable condition for cyanobacteria to grow. However, it remains to be determined whether TP, TN, DIN, and DIP have different influences on cyanobacteria growth and if low DIN:TP is more accurate than low TN:TP as an indicator for cyanobacteria peaks in Lake Vombsjön.
The long-term time series of samples from Lake Vombsjön demonstrates a clear seasonal pattern in the TN:TP ratio, where TN:TP in the outlet decreased more than in the inlet from June and onwards. Before the end of June, the TN:TP ratio in the outlet was in general above 50 and during the rest of the year the ratios were below 20 (Figure 2). The former might indicate the lake water at the first half of the year under P limiting conditions, whereas the latter might indicate N limiting conditions. A similar pattern was observed in the Great Lakes of the USA [47]. It might further indicate that the dominance of cyanobacteria during summer and autumn (Figure 1b) was caused by a transition from phosphorus to nitrogen limiting conditions. One of the likely reasons behind the seasonal pattern in TN:TP ratios, which declines during the summer and autumn (Figure 2), might be the increase of phosphorus concentrations at the outflow of the lake (See Figure S3), possibly caused by phosphorus leakage from the sediment (resulting in internal phosphorus loading). At the same time, N depletion in the autumn also contributed to the decrease in TN:TP ratios (See Figure S4).
The correlation between cyanobacteria biomass and TP, TN, DIP, and DIN in Lake Vombsjön shows that TP has a stronger positive correlation with cyanobacteria biomass than DIP, and that DIN has a stronger negative correlation with cyanobacteria biomass than TN. Therefore, DIN:TP predicts cyanobacteria biomass development better than TN:TP (Table 1 and Figure 3, Figure 4 and Figure 5). Low DIN corresponded to high cyanobacteria biomass, suggesting that certain cyanobacteria thrive under nitrogen limiting conditions. This might also reflect the autumn (September) situation characterized by more nitrogen limiting conditions. Morris and Lewis (1988) supported that TP is better than dissolved phosphorus for P availability measurements as it includes internal stores of P, while dissolved nitrogen is better than TN for availability measurements, as TN includes various non-available components, whereas luxury uptake of N is limited [48]. This may explain why cyanobacteria dominate when there are large amounts of dissolved phosphorus released from the sediment that coincide with very limited dissolved nitrogen availability in the lake. As discussed by Dolman and Wiedner, DIN/TP might be a better indicator of nutrient limitation than TN:TP and the influence of nitrogen on freshwater phytoplankton biomass might need more attention [49]. Previous empirical studies observed values of DIN/TP ratios in the range of 0.5–4 (mass) to discriminate between the outcomes of nutrient addition experiments and to do so better than the TN:TP [48,50]. Furthermore, it was shown that nitrogen availability might matter in the genetic regulation of toxin production as discussed by Steffen and others, wherein their statistical examination of Canadian lakes showed a correlation between microcystin concentration and low N:P ratios [48]. Hence this suggests that besides studying the phosphorus dynamics, it is crucial to also monitor DIN and understand how the nitrogen cycle is influencing cyanobacteria. In Lake Vombsjön, the highest amount of cyanobacteria biomass, >10 mm3, correspond to DIN/TP values of less than 10, whereas the lowest biomass are recorded when DIN/TP is above 50 (Figure 6). Hence, it may be concluded that trends in DIN/TP ratios may function as “early warning signals” for developing cyanobacterial blooms, suggesting that managers should be more aware of, and monitor, DIN/TP values, especially in late summer and autumn.

4. Conclusions

The long-term monitoring of Lake Vombsjön provides further understanding of the mechanisms behind cyanobacteria growth and blooms. Our study also highlights the importance of monitoring cyanobacterial blooms during the period from July to November, with a particular focus on September. Our findings suggest that reducing the amount of total phosphorus is a key for reducing the risk of cyanobacterial blooms, but that the nitrogen availability, such as DIN, plays a very important role for the phytoplankton dynamics and that cyanobacteria often dominate under N limiting conditions. DIN should be monitored more carefully than TN as it is a better indicator of nitrogen availability than TN. It is especially important to control TP under N depletion, as our data analysis also brought to light the importance of DIN/TP relative to that of TN:TP for extreme cyanobacteria bloom events, where a ratio of at least 10, but preferably above 50, is needed to curtail cyanobacteria dominating blooms.
To realize effective management practices to reduce nutrient for cyanobacteria prevention, many efforts are applied, such as improving the sewage system in the surrounding area [51] and reducing nutrient leakage from agriculture [52]. There are many options to obtaining control over the P levels, such as increasing the efficiency of the phosphorus uptake by crops in the farmland, recycling and reusing phosphorus in water bodies, and promoting efficient wastewater treatment, especially at individual wastewater treatment plants around Lake Vombsjön, which requires the involvement and investment of many cooperating stakeholders. In order to optimize the management of Lake Vombsjön and other lakes providing drinking water, we recommend monitoring and reduction of phosphorus and dissolved nitrogen in concert.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4441/10/7/919/s1, Figure S1: Location of Lake Vombsjön in Scania, Figure S2a: Multi-year dynamics (solid line) and trend (dashed line) in TN (blue) and TP (red) at the inlet of the Björkaån River (The main inlet of Lake Vombsjön), Figure S2b: Seasonal dynamics (solid line) and trend (dashed line) in TP and TN concentrations (µg/L) at the outlet of Lake Vombsjön, Figure S2c: Yearly differences in yearly TN and TP transport (kg/year) between the main inlet and the outlet of Lake Vombsjön during the period of 1999–2015, Figure S3: The average monthly dissolved phosphorus concentration (PO4-P µg/L) at the outlet of Lake Vombsjön during the period of 1999–2015, Figure S4: Average monthly values for the amount of TN and TP found in the main inlet and the main outlet of Lake Vombsjön during the period of 1999 to 2015.

Author Contributions

Conceptualization, J.L. and K.M.P.; Methodology, J.L.; Software, J.L.; Validation, J.L., K.M.P. and L.A.H.; Formal Analysis, J.L.; Investigation, J.L.; Resources, J.L.; Data Curation, J.L.; Writing-Original Draft Preparation, J.L.; Writing-Review & Editing, J.L., K.M.P. and L.A.H.; Visualization, J.L.; Supervision, K.M.P. and L.A.H.; Project Administration, K.M.P.; Funding Acquisition, K.M.P.

Funding

This research was funded by Formas—The Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning grant number 2017-00303. This project is also financially supported by Sydvatten and Sweden Water Research.

Acknowledgments

This work was mainly executed during Young Scientist Summer Program 2017 at IIASA, i.e. International Institute for Applied System Analysis. Many thanks to Professor Peter Burek for his kind supervision and the whole WATER group at IIASA for their support.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (a) Seasonal patterns of cyanobacteria biomass (mm3/L) in Lake Vombsjön during 1990 to 2002 (the blue line: 0.2 mm3/L is WHO (World Health Organization alert level 1 for drinking water waters; yellow line 1 mm3/L is Finnish drinking water for actions taken such as risk assessment and inform authorities; Red line is 10 mm3/L is WHO alert level 2 for drinking waters); (b) Seasonal patterns of cyanobacteria relative abundance found in Lake Vombsjön 1989–2002.
Figure 1. (a) Seasonal patterns of cyanobacteria biomass (mm3/L) in Lake Vombsjön during 1990 to 2002 (the blue line: 0.2 mm3/L is WHO (World Health Organization alert level 1 for drinking water waters; yellow line 1 mm3/L is Finnish drinking water for actions taken such as risk assessment and inform authorities; Red line is 10 mm3/L is WHO alert level 2 for drinking waters); (b) Seasonal patterns of cyanobacteria relative abundance found in Lake Vombsjön 1989–2002.
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Figure 2. Seasonal patterns of TN:TP (total nitrogen:total phosphorus) ratios at both inlet and the outlet of Lake Vombsjön.
Figure 2. Seasonal patterns of TN:TP (total nitrogen:total phosphorus) ratios at both inlet and the outlet of Lake Vombsjön.
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Figure 3. Comparison of the relation of dissolved inorganic phosphorus (DIP) with cyanobacteria biomass (dot red) and TP with cyanobacteria biomass (triangle blue).
Figure 3. Comparison of the relation of dissolved inorganic phosphorus (DIP) with cyanobacteria biomass (dot red) and TP with cyanobacteria biomass (triangle blue).
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Figure 4. Comparison of the relation of dissolved inorganic nitrogen (DIN) with cyanobacteria biomass (triangle blue) and TN with cyanobacteria biomass (dot red).
Figure 4. Comparison of the relation of dissolved inorganic nitrogen (DIN) with cyanobacteria biomass (triangle blue) and TN with cyanobacteria biomass (dot red).
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Figure 5. Comparison of the relation of DIN:TP with cyanobacteria biomass (triangle blue) and TN:TP with cyanobacteria biomass (dot red).
Figure 5. Comparison of the relation of DIN:TP with cyanobacteria biomass (triangle blue) and TN:TP with cyanobacteria biomass (dot red).
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Figure 6. Plot of DIN:TP and cyanobacteria biomass; it is likely to conclude that low DIN:TP (<10) corresponds cyanobacteria peaks.
Figure 6. Plot of DIN:TP and cyanobacteria biomass; it is likely to conclude that low DIN:TP (<10) corresponds cyanobacteria peaks.
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Table 1. Correlations between concentration of cyanobacteria and TN, DIN (dissolved inorganic nitrogen), TP, DP (dissolved phosphorus), TN:TP, and DIN:TP in Lake Vombsjön, and resulting p-values (Spearman’s rs).
Table 1. Correlations between concentration of cyanobacteria and TN, DIN (dissolved inorganic nitrogen), TP, DP (dissolved phosphorus), TN:TP, and DIN:TP in Lake Vombsjön, and resulting p-values (Spearman’s rs).
ItemTNDINTPDPTN:TPDIN:TP
Correlation Coefficient−0.56−0.650.620.31−0.63−0.66
p-Values<0.001<0.001<0.001<0.001<0.001<0.001

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Li, J.; Hansson, L.-A.; Persson, K.M. Nutrient Control to Prevent the Occurrence of Cyanobacterial Blooms in a Eutrophic Lake in Southern Sweden, Used for Drinking Water Supply. Water 2018, 10, 919. https://doi.org/10.3390/w10070919

AMA Style

Li J, Hansson L-A, Persson KM. Nutrient Control to Prevent the Occurrence of Cyanobacterial Blooms in a Eutrophic Lake in Southern Sweden, Used for Drinking Water Supply. Water. 2018; 10(7):919. https://doi.org/10.3390/w10070919

Chicago/Turabian Style

Li, Jing, Lars-Anders Hansson, and Kenneth M. Persson. 2018. "Nutrient Control to Prevent the Occurrence of Cyanobacterial Blooms in a Eutrophic Lake in Southern Sweden, Used for Drinking Water Supply" Water 10, no. 7: 919. https://doi.org/10.3390/w10070919

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