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Article

A Simple Model for a Fast Forewarning System of Brown Tide in the Coastal Waters of Qinhuangdao in the Bohai Sea, China

1
College of Civil Engineering, Tongji University, Shanghai 200092, China
2
Research Center of Harmful Algae and Marine Environment, Jinan University, Guangzhou 510632, China
3
CAS Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China
4
State Key Laboratory of Marine Geology, Tongji University, Shanghai 200092, China
5
The Lyell Centre for Earth and Marine Science and Technology, Institute for Infrastructure and Environment, Heriot-Watt University, Edinburgh EH14 4AS, UK
*
Authors to whom correspondence should be addressed.
Appl. Sci. 2022, 12(13), 6477; https://doi.org/10.3390/app12136477
Submission received: 25 May 2022 / Revised: 21 June 2022 / Accepted: 24 June 2022 / Published: 26 June 2022

Abstract

:
Qinhuangdao, a famous coastal resort city in northeastern China, has been affected by the rapid growth of harmful algae. The brown tide induced by Aureococcus anophagefferens (A. anophagefferens) first occurred along Qinhuangdao’s coastline in 2009, and it then developed into a harmful alga for the Bohai Sea. Based on MIKE 21, we construct a 2D coupled hydrodynamic and transport model to study the variation and distribution of total nitrogen (TN), and establish the relationship between A. anophagefferens, dissolved organic nitrogen (DON), and TN to provide a fast forewarning system for brown tide in Qinhuangdao. This model considers the decay, diffusion, and settling of TN, and the model results are in good agreement with the measured tidal level, current, and TN, indicating that the model is capable of capturing the observed TN distribution during the brown tide period. The transfer function relating TN to A. anophagefferens leads to a reliable fast forewarning and monitoring system. Moreover, the transferred A. anophagefferens cell density can be used to forecast the regional risk level of brown tide with a specific color indicator. The implementation of national policy relating to marine ecosystems decreases the nearshore concentration of N, P, and other nutrients, and therefore decreases harmful algal blooms. The fast routine assessment of brown tide by the present warning system provides robust guidance for the government to take action.

1. Introduction

Rapid industrialization and aquaculture have taken place during the past few decades in the Bohai Sea. The Bohai Sea has been one of the most important aquaculture areas in China since ancient times, producing more than 40% of the fishery resources of China. Qinhuangdao is located in Bohai Bay, a semi-closed area close to the M2 tide amphidromic point where the water is too slow to achieve self-purification [1]. Due to the high nutrient loads and organic wastewater discharges in surrounding areas and increasing sewage and industrial effluent in the aquaculture, the offshore water in Qinhuangdao is subject to frequent harmful algal blooms. Under high nutrient levels and sub-tropical temperatures, phytoplankton concentration can grow rapidly to an alarming level. Harmful tides typically last a few days to a week, depending on wind conditions, and lead to low dissolved oxygen in the bottom layer of the water [2]. Harmful algal blooms including brown tide have become more frequent, extensive, and severe worldwide [3,4,5].
Aureococcus anophagefferens (A. anophagefferens)-induced algal bloom events have received considerable attention for decades since their first occurrence in the 1980s along the eastern coast of the USA [6,7,8], and they were also found in the coastal bays of South Africa [9,10]. As a type of pico-sized red tide, this algal bloom has been named “brown tide” to distinguish it from traditional red tide [11], as it can discolor waters into a dark brown color. Brown tide is a discoloration of marine water due to the explosive reproduction or aggregation of planktonic algae, protozoa, or bacteria in the ocean driven by anomalous hydro-meteorological, hydrodynamic, and biological processes [12,13]. The brown tide induced by the A. anophagefferens in Qinhuangdao was first observed in the coastal waters near a scallop cultivation farms in 2009 [14,15,16,17], which motivated extensive investigations on the geographic and historical presence of this species in the seas of China. Tang et al. [18] investigated 3000 km of coastline and the 1500-year presence of A. anophagefferens and revealed that it is an indigenous species in Qinhuangdao. It took several years to confirm the causative species by microscopy, pigment chemotaxonomy, and genetic analyses [19]. Zhang et al. [12] found that all eight pelagophyte clones were similar to A. anophagefferens, which caused the brown tides along the coasts of the eastern Unites States and South Africa. Dissolved organic nitrogen (DON) and shellfish farms are mainly responsible for brown tide [20,21]. Brown tide outbreaks have become a major ecological hazard in the Bohai Sea, with significant impacts on the mariculture industry (scallops), coastal ecosystems [14,20], and zooplankton [22,23,24,25,26,27]. The main tributaries to Qinhuangdao Bay have been polluted to various degrees by industrial effluent, aquaculture wastewater, and domestic sewage. During brown tide events, peak A. anophagefferens concentrations were always observed along the Funing and Changli coast, where scallop cultivation farms are located in Qinhaungdao Bay.
Human activity-induced eutrophication offshore is well-recognized as the main cause of harmful algal bloom [28,29,30]. Lee and Qu [31] investigated algal blooms in Hong Kong and found that red tide can be formed under the right temperature, nutrient, and hydrodynamic conditions and transported to other locations. Zhang et al. [32] studied the relationship between A. anophagefferens distribution and environmental factors and found that certain temperature and salinity levels are required for intensive brown tide to occur in Qinhuangdao coastal water with high DON and low dissolved inorganic nutrients (DIN). Anderson et al. [28] and Glibert and Burford [33] found that eutrophication is induced by nutrient pollution close to the harmful algal area offshore. Eutrophication can impact the distribution and diversity of species and then change the preponderant algae. Wong et al. [34] proposed that algal blooms are strongly controlled by the interaction of physical and biological process. In a changing climate, an increased carbon dioxide concentration in the atmosphere is expected to intensify global warming and ocean acidification, therefore altering the distribution, frequency, and occurrence season of the red tide [35]. Brown tide events will become more frequent due to urbanization along the coast.
Previous studies into harmful algae mainly focused on species invasion or ecology deterioration. There is a lack of understanding of the formation and outbreak mechanisms of brown tide, which would be critical for establishing a reliable monitoring, forewarning, and treatment system for hot spots to prevent and reduce brown tide events. Gastrich [36] proposed a three-level hierarchy of effects of brown tide based on algal cell components. He used 35,000 and 200,000 cells/mL as concentration criteria to identify the risk level. Zhang et al. [37] used traditional modified clays to remove A. anophagefferens and found the removal efficiency to be low. Randhawa [38] used H2O2 to control brown tide in the laboratory and found that it can remove high-density A. anophagefferens efficiently, but the cost is high. In recent years, advanced technology has been developed to monitor harmful algae and to create a warning system. Remote sensing and satellite observations have been applied to track the spatial distribution and growth of algae. Numerical models have been applied to provide harmful algal warnings [39,40]. Using physical and chemical methods to treat brown tide and other harmful algal bloom events, however, is still in its infancy.
In this study, a coupled hydrodynamic and particulate transport model based on MIKE21 is employed to predict the temporal and spatial distribution of the total nitrogen (TN). This model considers the decay, diffusion, and settling of TN, and the model results are in a good agreement with the measured tidal level, current, and TN, which indicates that the model is capable of capturing the observed TN distribution during the brown tide period. A relationship between A. anophagefferens, dissolved organic nitrogen (DON), and TN is obtained from field observations and combined with numerical simulation results of TN to establish a fast forewarning system for brown tide in Qinhuangdao. The objective is to make full use of the observation data to establish a reliable relationship between A. anophagefferens and TN to represent the complex process of algal growth in order to provide fast alerts for the stakeholder. The main simulated area in this study is shown in Figure 1.

2. Materials and Methods

MIKE 21 was developed by the DHI Group and can continuously simulate tidal circulation and mass transport. In this study, we established a two-dimensional coupled hydrodynamic and mass transport model of Qinhuangdao using a flow model (FM) based on the flexible unstructured mesh method, which was developed for applications within oceanographic, coastal, and estuarine environments. The spatial discretization of the primitive equations was performed using an element-centered finite volume method. The spatial domain was discretized by the subdivision of the continuum into non-overlapping elements. The MIKE FM has been used in many studies, and the governing equations and details of this model can be found in the MIKE User Manual [41].

2.1. Study Area and Mesh

Brown tides commonly occur in summer, especially in July and August, along the Qinhuangdao coastline. This model included two parts with different scales. A double-level scheme of unstructured triangular meshes with different refinements and scales was set up as shown in Figure 2. The large mesh (Level 1) covered the whole Bohai Sea to ensure a correct tidal flow field, and it provided the water level and current boundary to the small mesh (Level 2). The small mesh covered Qinhuangdao coastal waters, including the main river outlets. The Bohai Sea model was driven by the time series of the tidal level at Dalian and Yantai (two ends of the open boundary in Figure 2) from the tidal table published by the National Marine Data and Information Service of China. The Qinhuangdao model was driven by the time series of the water level, current speed, and direction extracted from the computational results of the Bohai Sea model along three open boundaries. The boundary of the small mesh was from the Luan River to the Shi River Estuary, along the coastline with a length of 16.5 km in the northeast and 35.6 km in the southeast. The large and small meshes had 14,183 and 13,606 nodes with 23,419 and 25,301 elements, respectively. The mesh size generally decreased from the sea toward the coast and estuary when considering both computational time and accuracy.

2.2. Hydrodynamic Model

The transport model was based on the currents calculated by a hydrodynamic model. Given that the coverage area of brown tides is restricted to the shallow intertidal and sub-tidal zones, a 2DH model mesh was adequate to simulate the hydrodynamics of the study area, considering the balance of computational speed and model precision in Qinhuangdao [42,43]. The model solved the two-dimensional incompressible Reynolds-averaged Navier–Stokes equations with assumptions of Boussinesq and hydrostatic pressure. The computational mesh used in this research was unstructured triangular mesh with the spatial discretization adopting the cell-centered finite volume method. The continuity and momentum equations were converted into nonlinear shallow water equations by integrating them over depth, and the 2DH equations are shown as follows:
h t + h u x + h v y = h S
h u t + h u 2 x + h v u y = f v h g h η x h ρ 0 p a x g h 2 2 ρ 0 ρ x + τ s x ρ 0 τ b x ρ 0 F u + h u s S
h v t + h u v x + h v 2 y = f u h g h η y h ρ 0 p a y g h 2 2 ρ 0 ρ y + τ s y ρ 0 τ b y ρ 0 F v + h v s S
where t is the time; x and y are the Cartesian coordinates; u and v are the depth-averaged velocity components in the x and y directions; h is the sum of the still water depth, d, and the time-varying water level, η ; S is the discharge of the point sources; f is the Coriolis parameter related to the angular velocity of Earth’s rotation and the geographic latitude; g is the gravitational acceleration; ρ is the water density; ρ 0 is the reference water density; P a is the atmospheric pressure; τ s x and τ s y are the surface stresses induced by wind; τ b x and τ b y are the bottom stresses; F u and F v are the horizontal stress terms due to eddy viscosity; and u s as well as v s are the discharge velocities of the point sources.
The model adopted wet–dry dynamic boundary processing technology, and the critical water depths of dry and wet points were 0.005 m and 0.05 m, respectively. The computational time step was in the range of 0.1–30 s and was adjusted to meet the Courant–Friedrich–Lewy (CFL) condition with a limited value of 0.8 in the model calculation process, where C F L = ( g h + | u | ) Δ t Δ x + ( g h + | v | ) Δ t Δ y . The horizontal eddy viscosity coefficient used the Samagorinsky model to calculate the grid scale, and the Samagorinsky coefficient was 0.28. The initial velocity and water level were 0 m/s and 0 m, respectively. The Manning number was 74 m1/3/s, by which the model bed resistance was determined. Based on the Bohai Sea model, the boundary condition at the tidal inlet and open sea boundaries was adopted for the medium tidal range and Flather condition, respectively [42]. The boundary condition at the river outlet was set as the specified discharge value of 1 m3/s, and the initial condition was set as 0, including values of surface elevation, u-velocity, and v-velocity. The time step interval could self-regulate itself, ranging from 0.01 to 30 s to meet the CFL restriction as velocity changed with time at all computational nodes and time steps. The wind and temperature data were downloaded from the European Centre for Medium-Range Weather Forecasts (ECMWF (http://apps.ecmwf.int/datasets/data/interim-full-daily, accessed on 1 January 2021)) with a spatial resolution of 0.25°.

2.3. Transport Model

We set the TN as a component of the transport model. There was no dispersion across open boundaries, as the gradient of the concentration here was assumed to be 0. The linear decay of a component is generally defined as:
c t = k c
where c is the specific concentration and k is the decay constant.
For simulating the variation of TN distribution, after conducting many tests, we set the parameter of decay as 1.157 × 10−7/s. The time step was the same as that of the hydrodynamic simulation. The initial component of TN was set as 5 mg/L according to the measured data. The discharge and TN components of the main rivers were based on the field-measured data collected.

2.4. Model Validation

Field observations of tidal level and current were used to verify the hydrodynamic model. The water levels were collected from the Shanhaiguan station during the spring tide (11–12 May 2013) and neap tide (16–17 May 2013). The current data were collected at five field stations, SDL01 to SDL05, during the neap tide, 16–17 May 2013. These observation stations are shown in Figure 1. Figure 3 shows the comparison of simulated results and measured data including tidal level and current speed and direction. The hydrodynamic model results were quantitatively assessed against observed values using the skill model [44].
s k i l l = 1 | X m X o | 2 ( | X m X o ¯ | + | X o X o ¯ | ) 2
where D ¯ is the mean value, in situ, of the observed data; M and D are the computed result and in situ observed data, respectively; and N is the number of data entries. A skill value of 1.0 indicates a perfect performance of the model: skill between 0.65 and 1 is considered excellent, skill in the range of 0.5–0.65 is considered very good, skill in the range of 0.2–0.5 is considered good, and skill of less than 0.2 is considered poor.
The model results generally matched the measured values very well with the excellent performance of skill evaluation summarized in Table 1. The skill of tidal level at Shanhaiguan during the spring and neap tides were all 0.99, and those of current speed at SDL01, SDL02, SDL03, SDL04, and SDL05 were 0.90, 0.87, 0.85, 0.94, and 0.86, respectively. The skill values of current direction at the same stations were 0.97, 0.98, 0.95, 0.97, and 0.95, respectively. All skill values (over 0.90) were much larger than 0.65, implying the excellent predictive efficiency of the model.
In order to evaluate the transport model, which shares the same computational mesh as the hydrodynamic model of Qinhuangdao, the validated TN concentration data were collected from Qinhuangdao during the period 16–23 July 2013. The simulated result of TN concentration is shown in Figure 4. Given that the measured data at 20 stations were from different dates, the time series was discontinuous, we calculated the average error, and all of the numbers were below 11% (shown in Table 2), which means the present model can accurately predict the TN distribution.

3. Results

In this section, we firstly use the coupled hydrodynamic and transport validated model to simulate the TN concentration during the brown tide period in 2014. The TN concentration in the coastal water is mainly controlled by the seagoing rivers. We then find the relationship between the TN concentration and A. anophagefferens density by studying the observed data at 20 stations and transfer the TN to DIN, and then to A. anophagefferens. Furthermore, we establish an indicator system with four grades and provide appropriate measures for application.

3.1. TN Distribution during Brown Tide

Figure 5 shows the measured and simulated data of TN concentration at 20 stations. The simulation period is from March to September 2014 and includes two large-scale brown tide events in May and August, respectively. As we lack the seagoing rivers’ TN input data for 2014, considering that there are no large construction projects and the climate only changed slightly, we use the data for 2013 to take the place of the data for 2014. We can see that the result shows a certain deviation, which may be mainly caused by the difference in TN concentration from 2013 to 2014 in the seagoing rivers. Although there is this weakness, the simulation deviation is controlled at 26%, indicating that the results are reasonably convincing. Figure 6a presents the distribution of TN during the brown tide period in 2014, and Figure 6b depicts the satellite-observed bloom-area for the same period. We can see that these two figures are similar to each other in the abnormal area, although the simulated one covers more area, which demonstrates that the TN is correlated with brown tide. It is shown that, in the coastal area, the TN concentration is higher than that of the open sea, indicating that there is a higher risk along the coastline of having an algal bloom event.

3.2. Transfer Function from TN to A. anophagefferens

A. anophagefferens is a tiny, spherical and nonmotile picoplanktonic (cell size 2–3 µm) pelagophyte with no flagella [18,45]. A. anophagefferens cells were abundant during the brown tide period in Qinhaungdao coastal waters, which can be seen as an indicator of brown tide. Zhang et al. [32] reported that A. anophagefferens abundance was strongly positively correlated with nitrite and temperature. DON is commonly thought of as the main nitrite resource, and it is vital for improving A. anophagefferens-induced brown tide [46,47]. Since nitrogen is routinely monitored as a chemical element discharged from rivers to sea along the coastline in Qinhaungdao, we seek the relationship between A. anophagefferens density and TN concentration through their correlations with DON.
We analyzed the measured data from June 2013 to August 2014, which included two large-scale brown tide events (May 2013 and August 2014) in the sea area. The observation data indicates strong correlation between A. anophagefferens cell density and DON and temperature (T). Figure 7 shows the relationship between the A. anophagefferens density (use the cells concentration to represent) and DON in 2013 and 2014 during the brown tide event periods. Commonly, a concentration of 5 × 107 cells/L is thought of as the warning indication value to represent brown tide, and we use red circles to mark these values in this figure. As shown in Figure 7a, the density of A. anophagefferens cells increases when the concentration of DON is in the range of 0.00 ~ 40.00   μ mol / L and the value reaches a relatively high grade. Therefore, we narrow the range of DON concentration to 10.00 ~ 30.00   μ mol / L and find that the density of A. anophagefferens distributes in every value, which implies that the DON concentration is not the only main factor that influences the A. anophagefferens cell density in this range. When the range continuously narrows to 30.00 ~ 40.00   μ mol / L , the measured data reduce but the density of A. anophagefferens cells significantly increases, showing that the DON concentration varies in this range and it becomes the main factor of A. anophagefferens cell growth. In Figure 7b, the data in 2014 are similar to the data collected in 2013, showing that the A. anophagefferens cells rapidly grow in the range of 30.00 ~ 40.00   μ mol / L , and the concentration is higher than the indicated value. As can be seen in the range of 50.00 ~ 60.00   μ mol / L , there is also a point above the warning indication concentration, which means the brown tide can still bloom. However, if the DON concentration is lower than 20.00   μ mol / L , the possibility of bloom becomes lower, indicating that a low concentration can inhibit the propagation of A. anophagefferens. Combined with Figure 6a, although the data for DON are finite, the range of DON concentration from approximately 20.00 to 60.00 µmol/L can be seen as the sensitive range for inducing brown tide. With the DON concentration increase, a higher A. anophagefferens cell density can cause the brown tide event with more certainty.
Separately drawing the fitting relationship in Figure 7a,b, we can see that, in Figure 7b, the data are substantial and the time covers four months, providing greater accuracy than in Figure 7a. So, we preliminarily choose the fitting equation of the data in 2014 to establish the relationship of A. anophagefferens cell density and DON concentration as an exponential function:
ρ = 5000 e 0.24 D O N
where ρ is the A. anophagefferens cell density.
In this study, temperature is not the main factor affecting the transformation, but for rigor and accuracy, we still clarify it in this section and set the most appropriate value in the numerical model. We also draw a relationship between the temperature (T) and A. anophagefferens cell density in Figure 8. A. anophagefferens concentration reaching the warning indication level in the range of 10~23 °C is rare; however, in the range of 23~28 °C, the concentration rapidly increases. From Figure 8, we can obviously see that the most appropriate temperature for A. anophagefferens growth is around 23~26 °C, which is slightly higher than the study that gave the appropriate temperature as ranging from 21.5 to 23.2 °C [32].
Based on the correlation between the A. anophagefferens cell density and DON concentration during the brown tide periods, we tried to explore the correlation between A. anophagefferens cell density and TN concentration in the long-term measured data. There are no sufficient data, so we used the existing data to analyze the correlations of TN–DIN and DIN–DON and then transferred the relationship to TN concentration–A. anophagefferens cell density to obtain the mechanism of TN concentration’s effect on A. anophagefferens growth.
Figure 9 shows the relationship between the measured concentration of DIN and TN at 20 stations (time series are from June to July in 2013 and from April to August in 2014; positions are shown in Figure 1b). The intercepts are all set as 0, because the DIN and DON are also 0 mg/L when the TN concentration is 0 mg/L. All determination coefficients (R2) are above 0.53, indicating that the fitting relationships are reasonable. The slope of every station is summarized in Table 3, and the average value is 0.195.
Based on the measured data of TDN, DIN, and DON, we also draw the fitting curves of DIN–TDN and DON–TDN and calculate R2 using the same methods. All determination coefficients (R2) shown in Figure 10 are above 0.82, indicating that the fitting relationships are good. The average slope values of DIN–TDN and DON–TDN, as shown in Table 4, are 0.450 and 0.550, respectively. Furthermore, we transfered these two groups of relationship to establish that the slope of DON–DIN is 1.222. Combined with the slope of DIN–TN, we finally obtain that the averaged DON/TN is 0.238.
Based on the correlation of DON–TN and DON–A. anophagefferens cells, we derived the fitting equation of A. anophagefferens cell density and TN concentration as below:
ρ = 5000 e 4.087 T N

3.3. Fast Forewarning System of Brown Tide

The brown tide in the coastal area of Qinhuangdao was induced by DON and shellfish aquaculture [16,20] and, conversely, the brown tide also influences the shellfish. The brown tide in 2009 resulted in shellfish death in two out of three of the mariculture areas in Qinhaungdao. Meanwhile, the brown tide event in 2010 covered more than 3350 km2, which caused the pecuniary loss of more than 0.2 billion RMB [48]. We indirectly transferred the DON concentration to the A. anophagefferens cell density using the TN concentration as mentioned before.
According to the current situation, we separated the system into four grades in Table 5 to help the government to take appropriate measures to prevent brown tide from occurring or spreading. This system setup uses the relationship between TN and A. anophagefferens density on the basis of the transport model results to compartmentalize grades. Green represents good water quality, and the government should only conduct routine monitoring; meanwhile, when the water quality worsens and brown tide occurs, it needs to take appropriate measures.
Meanwhile, we have highlighted the transferred A. anophagefferens distribution in August 2014 with the appropriate color in Figure 11. It is clear that A. anophagefferens density in this period for most of the area offshore is in the range of approximately 5 × 105 to 5 × 106 cell/L, in the system shown as the third degree. However, there is also a small area in the range of 5 × 106~5 × 107 cell/L close to the seagoing rivers, which is indicated as second degree, meaning that the government needs to take relevant measures to address this higher concentration.
Although this forewarning system uses a simple mechanism and model, it still provides a fast prediction for brown tide outbreaks and helps to carry out total management in the mariculture areas. The system uses routine monitoring data as the input, which is convenient for operation. Meanwhile, the result indicator provides different degrees of warning for the government to quickly conduct monitoring in the key areas of potential risk and take appropriate actions in mitigating brown tide.

4. Discussion

4.1. Impact of Nutrients on Brown Tide

During the Thirteenth Five-Year-Plan period, the Science and Technology Ministry of China conducted special studies on typical harmful algal blooms in offshore areas. In 2017, a project examining the formation mechanism, monitoring, and forecasting and estimate technology of red tide (include brown tide) started. Aiming at algal bloom in offshore areas, many scholars have conducted studies into monitoring and water environmental treatment. Using modified clays is an important technique for the mitigation of harmful algal blooms, especially the red tide [49], and has been successfully applied in offshore red tide management in China, greatly improving coastal water quality. Hebei province has promulgated the plan for comprehensive control in the Bohai Sea and advocated improving the marine environmental risk monitoring and forecasting and emergency management capability. Policy demands that in the ecologically fragile region and the brown tide-prone area, the feeding aquaculture model is forbidden. Meanwhile, carrying out the risk assessment of emergencies in coastal cities to improve the ability of the government to prevent environment risk events is also a vital measure. All of these measures have great effects on reducing harmful algal bloom. Figure 12 shows the occurrence number of red tide (include brown tide) and the coverage of A. anophagefferens from 1990 to 2020 (data collected from the Bulletin of China Marine Disaster, http://www.mnr.gov.cn/sj/sjfw/hy/gbgg/zghyzhgb/, accessed from 26 November 1990 to 26 April 2021. [48]). It is obvious that, after undertaking the relevant measures, the algal bloom decreased sharply, and the ecological environment was improved.
Sufficient nutrients and low grazing pressure by zooplankton and scallops can accelerate the growth of small-celled phytoplankton [50], including A. anophagefferens. Previous studies have revealed the nutrient effects on brown tide blooms. As one of the dominant species in brown tide, A. anophagefferens has a considerable contribution to phytoplankton abundance [15,51] because it can outcompete other phytoplankton in the presence of elevated organic matter concentration [52]. The decreasing concentration of DIN, increasing human aquaculture activities, and suitability of summer temperatures for the growth of A. anophagefferens may be the primary causes of brown tide outbreaks [53]. Zhang et al. [54,55] analyzed the in situ data of the stations in Qinhuangdao and found that the DOP (dissolved organic phosphorus) can restrain A. anophagefferens growth, while DON showed great importance in causing brown tide.
With the continuous increase in the amount of national attention paid to the marine ecological environment, the concentration of nutrients, including nitrogen, in the seagoing rivers has significantly reduced. Considering the appropriate temperature, we can see that brown tide always blooms in summer, so the predicted time period is set from April to September. Therefore, we simulated the TN and transferred it into A. anophagefferens density to investigate the possibility of brown tide in recent years. We selected the TN concentration of July, August, and September in 2021 to convert into A. anophagefferens cell density (Figure 13). Although there exists a slightly higher area offshore compared to the open sea, it does not achieve the warning grade, indicating that this period experienced no danger of brown tide outbreak, and therefore the government just needed to conduct routine monitoring. The model results combine the transformation records, showing that water environment improvements reduced the degree of eutrophication to prevent brown tide from occurring in 2021.

4.2. Comparison with Other Forewarning Systems

The aim of this study is mainly to provide a simple fast forewarning system for brown tide. A similar method was also studied by Guo et al. [56] in their forewarning system, with the indicator of Chl-a by establishing a coupled physical-chemistry-eco-hydrodynamic module to simulate the growth, development, and decline of harmful algal bloom. The method for monitoring red tide and green tide has developed over many years, but brown tide has rarely been studied. Nowadays, satellite technology can enable the large-scale simultaneous monitoring of green tide [57]. During the bloom period in the Huanghai Sea, the satellite data of MERSI and HJ/CCD were applied to monitor green tide migration [58]. Allen et al. [59] took advantage of satellites combined with a model to monitor the chlorophyll and presented the medium resolution continental shelf (MRCS) to forecast red tide events. Sivapragasam et al. [60] established a numerical model using genetic programming and predicted the red tide event in Tolo Harbor in Hong Kong. Dippner et al. [61] presented a numerical model based on the HAMSOM model and the Lagrangian red-tide model. With the rapid development of computer technology and artificial intelligence, neural network models have gradually been applied to harmful algal bloom forecasting systems. Ma et al. [62] applied modified three-layer back propagation to forecast Noctiluca scintillans-induced red tide, and it performed well in reality. Velo-Suárez and Gutiérrez-Estrada [63] combined principal component analysis and a feed forward neural network to predict red tide bloom. However, the neural network model has a projecting defect of overdependence on the sample size, which may decrease the adaptability and tolerance. In recent years, harmful algal coupled monitoring and forecasting systems have drawn high levels of attention around the world [64]. Europe and some East Asian countries have distributed these systems, and the most important aim of these systems is to monitor for different kinds of algae [65].
For a fast forewarning system of brown tide in Qinhuangdao, a simple model, based on the 2D hydrodynamic and transport module to simulate the TN concentration, is adopted in the shallow coastal water where brown tides often occur in the summer season. A relationship between A. anophagefferens and TN obtained from field-measured data, combined with TN distribution from the transport module considering the decay, diffusion, and settling of TN, provided a fast forewarning system of brown tide in Qinhuangdao coastal water. This simple fast forewarning system of brown tide has been successfully used in Qinhuangdao and provided the local government with the ability to quickly conduct monitoring in the key areas of potential risk and take appropriate actions to mitigate brown tide. However, it has been proven by many previous studies that the vertical nutrient condition also plays a vital role in affecting harmful algal bloom [33]. In addition to nutrients, some other pressure variables, such as salinity, temperature, and the distribution of Chl-a, influence A. anophagefferens growth, migration, and spatiotemporal distribution [32]. Hence, a 3D-coupled model involving a hydrodynamic model, an ecological model, and a particle tracking model should be further established to simulate the real process of A. anophagefferens-induced brown tide, which is expected to be developed in following studies to improve the forewarning system.

5. Conclusions

In this study, the A. anophagefferens-induced brown tide in Qinhuangdao was investigated using a coupled hydrodynamic and particulate transport model based on MIKE 21. The hydrodynamic model was executed using a two-nested mesh system with different refinements and scales for the domains of the Bohai Sea and Qinhaungdao, respectively, and to predict the current to drive the transport model. This model considers the decay, diffusion, and settling of TN, and the model results are in good agreement with the measured tidal level, current, and TN, and thus the model is reliable. A relationship between A. anophagefferens, DON, and TN is obtained from field-measured data. This relationship and the numerically simulated TN distribution in Qinhuangdao can provide a fast forewarning system for brown tide. The fast routine assessment of brown tide by the present warning system provides robust guidance for the government to take action.
Due to the government having implemented various measures to protect the marine environment from harmful algal blooms, brown tide has been successfully mitigated in recent years. It is known that brown tide is not only affected by the A. anophagefferens cell density, but also by the vertical distribution of salinity and microorganisms; therefore, obtaining a better understanding of the mechanism of brown tide outbreak is of great importance. The present warning system only considers the single indicator of A. anophagefferens cell density, which has its limitations, and we will further improve it with a 3D model and neural networks and remote sensing technology.

Author Contributions

Conceptualization, C.K. and J.W.; methodology, C.K. and J.W.; software, J.W., J.F. and R.Q.; validation, J.W. and J.F.; investigation, L.O. and Q.Z. (Qingchun Zhang); data curation, L.O. and Q.Z. (Qingchun Zhang); writing—original draft preparation, J.W. and C.K.; writing—review and editing, C.K. and Q.Z. (Qingping Zou); supervision, C.K. and Q.Z. (Qingping Zou); funding acquisition, C.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Key Research and Development Project of China, under contract no. 2019YFC1407900, and the National Natural Science Foundation of China, under contract no. 41976159.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are sincerely grateful to the Eighth Geological Brigade of the Hebei Geo-logical Prospecting Bureau for supporting the fieldwork and measured data for the model validation. The last author has been supported by NERC, grant NE/V006088/1.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (a) The Bohai Sea area; (b) the main study area and the field observation stations (the black circle represents the tidal level station, the red triangles are the current stations, and the blue pentagrams show the position of TN stations). (c) Google Earth view of Qinghuangdao and the Bohai Sea.
Figure 1. (a) The Bohai Sea area; (b) the main study area and the field observation stations (the black circle represents the tidal level station, the red triangles are the current stations, and the blue pentagrams show the position of TN stations). (c) Google Earth view of Qinghuangdao and the Bohai Sea.
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Figure 2. The nested model domain and mesh. (a) The regional model domain and mesh of the Bohai Sea; (b) The local model domain and mesh of Qinhuangdao.
Figure 2. The nested model domain and mesh. (a) The regional model domain and mesh of the Bohai Sea; (b) The local model domain and mesh of Qinhuangdao.
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Figure 3. Model validation of tidal level and current velocity.
Figure 3. Model validation of tidal level and current velocity.
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Figure 4. Verification of the TN concentration.
Figure 4. Verification of the TN concentration.
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Figure 5. The simulated results compared with measured data at selected stations in May 2014.
Figure 5. The simulated results compared with measured data at selected stations in May 2014.
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Figure 6. (a) The distribution of TN concentration during the brown tide period in May 2014. (b) The satellite-observed brown tide area in May 2014.
Figure 6. (a) The distribution of TN concentration during the brown tide period in May 2014. (b) The satellite-observed brown tide area in May 2014.
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Figure 7. The relationship between A. anophagefferens cell density and DON in 2013 (a) and 2014 (b).
Figure 7. The relationship between A. anophagefferens cell density and DON in 2013 (a) and 2014 (b).
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Figure 8. The relationship between T and A. anophagefferens density from June to July in 2013.
Figure 8. The relationship between T and A. anophagefferens density from June to July in 2013.
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Figure 9. The relationships between DIN and TN at 20 stations from June 2013 to August 2014 derived from the field observations at station X1 to X5 and C1 to C15.
Figure 9. The relationships between DIN and TN at 20 stations from June 2013 to August 2014 derived from the field observations at station X1 to X5 and C1 to C15.
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Figure 10. The relationships of DIN–TDN and DON–TDN at 20 stations from June 2013 to August 2014.
Figure 10. The relationships of DIN–TDN and DON–TDN at 20 stations from June 2013 to August 2014.
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Figure 11. (a) The distribution of TN concentration in August 2014; (b) the transformation results from TN concentration to A. anophagefferens cell density, and amplification of the bloom area (c).
Figure 11. (a) The distribution of TN concentration in August 2014; (b) the transformation results from TN concentration to A. anophagefferens cell density, and amplification of the bloom area (c).
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Figure 12. The occurrence number of red tide (a) and the A. anophagefferens coverage during the brown tide period (b) from 1990 to 2020.
Figure 12. The occurrence number of red tide (a) and the A. anophagefferens coverage during the brown tide period (b) from 1990 to 2020.
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Figure 13. The distribution of A. anophagefferens cell distribution in July, August, and September 2021.
Figure 13. The distribution of A. anophagefferens cell distribution in July, August, and September 2021.
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Table 1. Hydrodynamic model evaluation.
Table 1. Hydrodynamic model evaluation.
VariableTimeStationPeriodSkillPerformance
tidal levelMay, 2013Shanhaiguan StationNeap tide0.99excellent
Spring tide0.99excellent
speedMay, 2013SDL01Neap tide0.90excellent
SDL020.87excellent
SDL030.85excellent
SDL040.94excellent
SDL050.86excellent
directionMay,2013SDL01Neap tide0.97excellent
SDL020.98excellent
SDL030.95excellent
SDL040.97excellent
SDL050.95excellent
Table 2. The average error of TN for July 16–18 2013.
Table 2. The average error of TN for July 16–18 2013.
TimeAverage Error of Station Groups (%)
X GroupC Group
16 July 20134.052.40
18 July 20133.738.60
23 July 20136.648.81
25 July 201310.4510.45
Average6.227.57
Table 3. The slope of fitted linear relationship between DIN and TN at 20 stations from June 2013 to August 2014.
Table 3. The slope of fitted linear relationship between DIN and TN at 20 stations from June 2013 to August 2014.
StationsDIN/TNStationsDIN/TNStationsDIN/TNStationsDIN/TN
C10.239C60.186C110.195X10.243
C20.166C70.179C120.214X20.217
C30.169C80.155C130.198X30.186
C40.193C90.200C140.155X40.263
C50.224C100.170C150.146X50.208
Average value0.195
Table 4. Summary of the values of DIN/TDN and DON/TDN.
Table 4. Summary of the values of DIN/TDN and DON/TDN.
PeriodDIN/TDNDON/TDN
June to July 20130.3850.615
April to August 20140.5150.485
Average0.4500.550
Table 5. The brown tide warning and fast forecast monitoring indicator of A. anophagefferens density.
Table 5. The brown tide warning and fast forecast monitoring indicator of A. anophagefferens density.
A. anophagefferens Density ( C e l l s / L ) GradeRepresent ColorMeasures
< 5 × 10 5 SafeGreenConduct routine monitoring
5 × 10 5 ~ 5 × 10 6 Third-degreeYellowConduct Third-degree forecast
5 × 10 6 ~ 5 × 10 7 Second-degreeOrangeWarning for shellfish aquaculture
> 5 × 10 7 First-degreeRedBrown tides—Conduct emergency handling for shellfish aquaculture
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Wang, J.; Kuang, C.; Ou, L.; Zhang, Q.; Qin, R.; Fan, J.; Zou, Q. A Simple Model for a Fast Forewarning System of Brown Tide in the Coastal Waters of Qinhuangdao in the Bohai Sea, China. Appl. Sci. 2022, 12, 6477. https://doi.org/10.3390/app12136477

AMA Style

Wang J, Kuang C, Ou L, Zhang Q, Qin R, Fan J, Zou Q. A Simple Model for a Fast Forewarning System of Brown Tide in the Coastal Waters of Qinhuangdao in the Bohai Sea, China. Applied Sciences. 2022; 12(13):6477. https://doi.org/10.3390/app12136477

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Wang, Jie, Cuiping Kuang, Linjian Ou, Qingchun Zhang, Rufu Qin, Jiadong Fan, and Qingping Zou. 2022. "A Simple Model for a Fast Forewarning System of Brown Tide in the Coastal Waters of Qinhuangdao in the Bohai Sea, China" Applied Sciences 12, no. 13: 6477. https://doi.org/10.3390/app12136477

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