Abstract
Water eutrophication has become a worldwide environmental problem in recent years, and understanding the mechanisms of water eutrophication will help for prevention and remediation of water eutrophication. In this paper, recent advances in current status and major mechanisms of water eutrophication, assessment and evaluation criteria, and the influencing factors were reviewed. Water eutrophication in lakes, reservoirs, estuaries and rivers is widespread all over the world and the severity is increasing, especially in the developing countries like China. The assessment of water eutrophication has been advanced from simple individual parameters like total phosphorus, total nitrogen, etc., to comprehensive indexes like total nutrient status index. The major influencing factors on water eutrophication include nutrient enrichment, hydrodynamics, environmental factors such as temperature, salinity, carbon dioxide, element balance, etc., and microbial and biodiversity. The occurrence of water eutrophication is actually a complex function of all the possible influencing factors. The mechanisms of algal blooming are not fully understood and need to be further investigated.
Keywords: Eutrophication mechanisms, Influencing factors, Nutrient enrichment, Assessment criterion, Water quality
INTRODUCTION
Water eutrophication is one of the most challenging environmental problems in the world. The increasing severity of water eutrophication has been brought to the attention of both the governments and the public in recent years. The mechanisms of water eutrophication are not fully understood, but excessive nutrient loading into surface water system is considered to be one of the major factors (Fang et al., 2004; Tong et al., 2003). The nutrient level of many lakes and rivers has increased dramatically over the past 50 years in response to increased discharge of domestic wastes and non-point pollution from agricultural practices and urban development (Mainstone and Parr, 2002). For more than 30 years, nutrient enrichment, especially phosphorus (P) and nitrogen (N), has been considered as a major threat to the health of coastal marine waters (Andersen et al., 2004). Once a water body is eutrophicated, it will lose its primary functions and subsequently influence sustainable development of economy and society. Therefore, nowadays the solution of water eutrophication and recovery of the multiple functions of the water system have become the key issues for environmental biologists. The main purpose of this paper is to provide a brief review on recent advances on understanding the mechanisms of water eutrophication and progresses in identifying the influence factors inducing water eutrophication.
DEFINITION AND OCCURRENCE OF WATER EUTROPHICATION
Definition of water eutrophication
Lakes and estuaries accumulating large amounts of plant nutrients are called “eutrophic” (from the Greek words eu meaning “well” and trophe meaning “nourishment”). Eutrophication can be defined as the sum of the effects of the excessive growth of phytoplanktons leading to imbalanced primary and secondary productivity and a faster rate of succession from existence to higher serial stage, as caused by nutrient enrichment through runoffs that carry down overused fertilizers from agroecosystems and/or discharged human waste from settlements (Khan and Ansari, 2005). Water eutrophication can be greatly accelerated by human activities that increase the rate of nutrient input in a water body, due to rapid urbanization, industrialization and intensifying agricultural production. For lake aquatic ecosystems, human activities in the watershed can lead to loss of dominant species and functional groups, high nutrient turnover, low resistance, high porosity of nutrients and sediments, and the loss of productivity (Liu and Qiu, 2007). For example, aquaculture is one of many human activities contributing to the environmental decline of coastal waters and the collapse of fisheries stocks worldwide (Alongi et al., 2003). Because the influence of the human activities, excessive nitrogen, phosphorus and other nutrients are loaded into water bodies like lake, reservoirs, embouchure and bay, which could cause negative ecological consequences on aquatic ecosystem structures, processes and functions, result in the fast growth of algae and other plankton, and deteriorate water quality (Western, 2001). Generally speaking, water eutrophication is caused by the autotrophy algae blooming in water, which composes its bioplasm by sunlight energy and inorganic substances through photosynthesis—the process of eutrophication is described as follows:
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According to above equation, it can be concluded that inorganic nitrogen and phosphorus are the major control factors for the propagation of algae, especially phosphorus. The Florida Everglades, a wetland of international importance, has been undergoing a significant shift in its native flora and fauna due to excessive total phosphorus (TP) loadings (an average of 147 ton per annum from 1995 to 2004) and an elevated mean TP concentration (69 μg/L of TP in 2004) from agricultural runoff and Lake Okeechobee outflow despite the use of over 17 000 ha of stormwater treatment areas (Richardson et al., 2007).
Assessment of water eutrophication
Surface water quality guidelines have been improved in recent years. The parameters to assess the ambient surface water quality have been increased. In China, the parameters for assessing environmental quality of surface water have been increased to over 30 (CNEPA, 2002). Five classes of surface water quality have been set up, and some selected parameters for assessing water quality of lakes or reservoirs are shown in Table 1. However, there are no perfect evaluation criteria for assessing water eutrophication. Generally, the physical and chemical evaluation parameters were used to assess water eutrophication, mainly nutrient concentration (N and P), algal chlorophyll, water transparency and dissolved oxygen. Although there are many different assessment parameters, the concentrations of total nitrogen and phosphorus are the two basic ones. Cheng and Li (2006) used total nutrient status index (TNI) to assess eutrophication status of lakes. The calculation of total nutrient status index is as follows:
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where, TNI is the sum of indexes of all nutrient parameters, TNIj is the TNI of j parameter, Wj is the proportion of j parameter in the TNI, and rij is the relation of chlorophyll a (Chla) to other parameters. The available parameters concerned include total nitrogen (TN), total phosphorus (TP), Chla, dissolved oxygen (DO), chemical oxygen demand by K2MnO4 oxidation method (CODMn), biological oxygen demand (BOD5), etc., and TN, TP and Chla are selected for calculating the TNI (Cheng and Li, 2006). Table 2 shows the burthen values of TN, TP and TNI in various eutrophicated water. It has been shown that the eutrophication or red tide occurs when N concentration in water reaches 300 μg/L and P concentration reaches 20 μg/L. Richardson et al.(2007) reported that exceeding a surface water mean TP threshold concentration of 15 μg/L causes an ecological imbalance in algal, macrophyte and macroinvertebrate assemblages as well as slough community structure in the Everglades areas. Therefore, it is considered that a threshold zone (12~15 μg/L) of TP may be more realistic and protective for all trophic levels.
Table 1.
Items | Surface water quality classification |
||||
Class I | Class II | Class III | Class IV | Class V | |
Water temperature (°C) | Maximum week increase≤1; maximum week decrease≤2 | ||||
pH | 6~9 | ||||
DO (mg/L) | Saturation≥90% | ≥6 | ≥5 | ≥3 | ≥2 |
CODMn (mg/L) | ≤2 | ≤4 | ≤6 | ≤10 | ≤15 |
CODCr (mg/L) | ≤15 | ≤15 | ≤20 | ≤30 | ≤40 |
BOD5 (mg/L) | ≤3 | ≤3 | ≤4 | ≤6 | ≤10 |
TN (mg/L) | ≤0.2 | ≤0.5 | ≤1.0 | ≤1.5 | ≤2.0 |
NH3-N (mg/L) | ≤0.15 | ≤0.5 | ≤1.0 | ≤1.5 | ≤2.0 |
NO2-N (mg/L) | ≤0.06 | ≤0.1 | ≤0.15 | ≤1.0 | ≤1.0 |
TP (mg/L) | ≤0.01 | ≤0.025 | ≤0.05 | ≤0.1 | ≤0.2 |
Chlorophyll a | ≤0.001 | ≤0.004 | ≤0.01 | ≤0.03 | ≤0.065 |
Transparency (m) | ≥15 | ≥4 | ≥2.5 | ≥1.5 | ≥0.5 |
Escherichia coli (L−1) | ≤200 | ≤2000 | ≤10000 | ≤20000 | ≤40000 |
DO: dissolved-oxygen; CODMn: Chemical oxygen demand by K2MnO4 oxidation method; CODCr: Chemical oxygen demand by chromium oxidation method; BOD5: Biological oxygen demand; TN: Total nitrogen; TP: Total phosphorus
Table 2.
Eutrophic status | TP (µg/L) | TN (µg/L) | Primary productivity | TNI | References |
Oligotropic water | 5~10 | 250~600 | 5~300 mg C/m2 | 0~30 | Likens et al.(1977); Cheng and Li (2006); Richardson et al.(2007) |
Moderately eutrophic | 10~30 | 500~1100 | 1000 mg C/(m2·d) | 31~60 | |
Eutrophic | 30~100 | 1000~2000 | − | 61~100 | |
Hypereutropic | >100 | >2000 | − | >100 |
TN: Total nitrogen; TP: Total phosphorus, TNI: Total nutrient status index
Inglett and Reddy (2006) reported evidences to support the use of stable C (delta C-13) and N (delta N-15) isotopic ratios as indicators for eutrophication and shifts between N and P limitation. Lin et al.(2006) compared the stable isotopes from dissolved nutrients and plants and water column nutrient parameters and integration of multiple proxies in a sediment core from Meiliang Bay of Taihu Lake, and found that differences in aquatic plant species and trophic status between East Taihu Bay and Meiliang Bay are indicated by their variations in delta C-13 and delta N-15 of aquatic plants and delta N-15 of NH4 +-N. A significant influence of external nutrient inputs on water quality of Meiliang Bay is reflected in temporal changes in delta N-15 of NH4 +-N and hydro-environmental parameters. The synchronous change between delta C-13 and delta N-15 values of sedimented organic matter (OM) has been attributed to elevated primary production at the beginning of eutrophication between 1950 and 1990, and then recent inverse correlation between them has been caused by the uptake of N-15-enriched inorganic nitrogen by phytoplankton grown under eutrophication and subsequent OM decomposition and denitrification in surface sediments, indicating that the lake has suffered from progressive eutrophication since 1990.
More sensitive biological indicators for assessing water eutrophication are needed to further study. Water eutrophication caused a degradation of healthy aquatic ecosystem, so the assessment methods and parameters should reflect the extents of aquatic ecosystem health. A set of ecological indicators including structural, functional and system-level aspects were proposed for a lake ecosystem health assessment, according to the structural, functional and system-level responses of lake ecosystems to chemical stresses including acidification, eutrophication, and copper, oil and pesticide contamination. The structural indicators included phytoplankton cell size and biomass, zooplankton body size and biomass, species diversity, macro- and micro-zooplankton biomass, the zooplankton/phytoplankton ratio, and the macrozooplankton/microzooplankton ratio. The functional indicators encompassed the algal C assimilation ratio, resource use efficiency, community production, gross production/respiration (i.e., P/R) ratio, gross production/standing crop biomass (i.e., P/B) ratio, and standing crop biomass/unit energy flow (i.e., B/E) ratio. The ecosystem-level indicators consisted of ecological buffer capacities, energy, and structural energy. Based on these indicators, a direct measurement method (DMM) and an ecological modeling method (EMM) for lake ecosystem health assessment were developed (Xu et al., 2001). The results of a case study demonstrate that both methods provided similar results which corresponded with the lake’s actual trophic state.
Occurrence of water eutrophication
The investigation from the UNEP (United Nation Environmental Protection) indicates that about 30%~40% of the lakes and reservoirs have been affected more or less by water eutrophication all over the world. Table 3 cites selected samples of water eutrophication occurrence in lake, reservoir, estuary and river in the world. Erie Lake is excessively rich in nutrients (Reutter, 1989), which has resulted in huge blooms of floating blue-green algae and the attached green alga, Cladophora spp. These blooms have rolled onto beaches in large mats resembling green steel wool. Water eutrophication has been reported in USA for Washington Lake (Welch and Crooke, 1987), Okeechobee Lake (Schelske, 1989), City Park Lake (Ruley and Rusch, 2002), etc. In Lugano Lake, between Italy and Switzerland, a faster rate of eutrophication was reported due to excessive discharges from human settlements around the lake, owing to population increase and immigration (Barbieri and Simona, 2001). The majority of Danish lakes are highly eutrophic due to high nutrient input from domestic sources and agricultural activities (Jeppesen et al., 1999). Garg et al.(2002) studied three lakes of Bhopal (Upper Lake, Lower Lake and Mansarovar Lake) in India, to assess the potential fertility of lentic waters and analyze the floral ecology. The highest level of eutrophication was found in Mansarovar Lake. The nutrient loading into the lake initially promoted the growth of phytoplanktons. Eutrophication constitutes a serious threat to many European lakes (Søndergaard et al., 2007), such as Pamvotis Lake in Northwest Greece (Romero et al., 2002), which has undergone cultural eutrophication over the past 40 years and is currently eutrophic. In South Africa, de Villiers (2007) reported that hypertrophic conditions indicated by TP levels prevail at least episodically at all of the Berg River monitoring stations; additionally, river water phosphate levels show a dramatic increase by a factor of more than 10 over the past 20 years, mainly due to anthropogenic inputs. Chivero Lake, Zimbabwe was reported to be hypertrophic and not sustainable (Nhapi, 2004). Sewage effluent is the major source of nutrients in the lake.
Table 3.
Water body | Nutrient (N, P) concentrations | Phytoplankton biomass | History of eutrophication | References |
Erie Lake, USA | TP: 115 μg/L | Chlorophyll a: 58 μg/L | Blu-green algae bloom between 1965 and 1979; Declined quality from 1995 | Reutter, 1989; Maggie, 2004 |
Okeechobee Lake, Florida, USA | TP: 50~100 μg/L | N and P are limitors for phytoplankton | Eutrophic at present | Schelske, 1989 |
City Park Lake, Louisiana, USA | TN: 682 μg/L, TP: 330 μg/L | Chlorophyll a: 35.1 μg/L | Eutrophic (2000~2001) | Ruley and Rusch, 2002 |
Lugano Lake | TP: 140 μg/L | Phytoplankton dry weight: 7~16 g/m2 | Strongly eutrophic from 1960s | Barbieri and Simona, 2001 |
Danish lakes | TN: 2.4 mg/L, TP: 0.37 mg/L | Chlorophyll a: 73 μg/L | Highly eutrophic | Jeppesen et al., 1999 |
Pamvotis Lake, Northwest Greece | TP: 0.11 μg/L, NH4+: 0.25 mg N/L, NO3−: 0.56 mg N/L | − | Cultural eutrophication over the past 40 years; Eutrophication at present | Romero et al., 2002 |
Berg River, South Africa | TN: 217 mg/L, TP: 70 mg/L | − | Hypertrophic | de Villiers, 2007 |
Chivero Lake, Zimbabwe | TN: 0.3~8.4 mg/L, TP: 1.01~5.01 mg/L | Chlorophyll a: 18.02~22.48 μg/L | Highly eutrophic since 1980s | Nhapi, 2004; Ndebele and Magadza, 2006 |
Taihu Lake, China | TN: 2.56~4.5 mg/L, TP: 0.25~0.35 g/L | Algae biomass: 2.7~6.4 mg/L | Class I/II in the early 1960s; Class IV in the mid-1990s; Now, inferior Class V | Ye et al., 2007; Jin et al., 2006 |
Songhua Lake, China | TN: 1.14~1.98 mg/L, TP: 0.038~0.102 mg/L | Algae density: 210.84×104~432.68×104 cell/L | Wang et al., 2004 | |
Dianchi Lake, China | TN: 2.13~8.27 mg/L, TP: 0.33~0.59 mg/L | − | Class III in the early 1970s; Now, inferior Class V | Guo and Sun, 2002 |
In China, water eutrophication occurred in 67 lakes (51.2% of the total lakes). Although the Boyanghu Lake and the Dongtinghu Lake are still mesotrophic at present, Dianchi Lake in Yunnan is possibly the most hypertropic lake in the world. In the early 1970s the water of Dianchi Lake was graded as Class III, now declined to the more inferior Class V (Lu et al., 2005). Taihu Lake, in China, has similar eutrophication issue. It is the third largest freshwater lake in China, located in the Yangtze River delta, one of the more developed areas of eastern China. In recent decades, because of severe pollution, water quality in Taihu Lake degraded from Class I/II in the early 1960s to Class II/III in the early 1980s and then to Class IV by the mid-1990s. At present, 83.5% of the lake area is eutrophic with an inferior Class V ranking (Liu and Qiu, 2007). The increasingly wider occurrence of excessive algae growth also begins earlier and lasts longer each year in Taihu Lake, and in the summer of 2007 an outbreak of blue algal bloom caused many drinking water treatment plants shut down and created a severe “water crisis event” in Wuxi City. Chaohu Lake is the fifth largest lake in China, located in central Anhui Province, and has a population of 2.3 million and more than 3000 factories in its basin. Since the 1990s, massive and rapid nutrient loading has made it one of the most eutrophic freshwater lakes in China. Jin et al.(2005) reported that eutrophic trend of Taihu Lake, Chaohu Lake and Xuanwu Lake in the region of the middle and lower valleys of Yangtze River was predicated using the ecological stress model. Provided the pollution water treatment rate is 60% in 2030, approximately 30 billion ton of polluted water would still be discharged directly into the lakes. Therefore, by 2030, all the urban lakes and most of the medium-sized lakes at the urban-rural fringe areas in China may be eutrophicated or hypertrophicated.
In the region of Yangtze River delta, 80% of the rivers have been polluted and the water quality cannot meet the standards of drinking water source. The degraded water quality mainly due to eutrophication in this region has resulted in extremely serious problems for drinking water supply. In Zhejiang Province about 36 out of 88 counties are suffering from the short supply of good drinkable water sources. In 2004, water eutrophication and algae blooming even occurred in the Qiantang River, which has the highest water flow velocity in China. High concentration of phosphorus and nitrogen is gradually causing eutrophication.
Water eutrophication in rivers occurs worldwide. During the past several decades, catastrophic losses in seagrass meadows have occurred worldwide, especially in flushed estuaries, coastal embayments and lagoons where nutrient loads are both large and frequent (Burkholder et al., 2007; Ralph et al., 2006). Coastal marine ecosystems of Northern Europe are under pressure from global change (e.g., nutrient enrichment), which threatens these resources (Gowen and Stewart, 2005). There are many statutory obligations and strong political pressures for greatly increased emphasis on the control of nutrients levels in UK rivers because of serious problem of water eutrophication (Mainstone and Parr, 2002). Within Europe, many national and international initiatives have been implemented in order to reduce the inputs and effects of nutrients in waters, e.g., the European Union’s Water Framework Directive (Andersen et al., 2004).
Harmfulness of water eutrophication
Generally speaking, the main harmfulness of water eutrophication is that it can break out the intrinsic equilibrium of the aquatic ecosystem and lead to the damage of the water ecosystem and the gradual degeneration of its functions. As a result, it can affect water quality and make transparency of water become worse than ever. Thus, little sunlight can penetrate water body and photosynthesis of plants under the water will be weakened or even stopped. Water eutrophication can also cause the supersaturation or lack of dissolved oxygen in water, which will be dangerous to aquatic animals and cause great death to them. Eutrophic systems tend to accumulate large amounts of organic carbon causing a shift in organic matter biochemical composition (Dell′Anno et al., 2002). Meanwhile, because of water eutrophication, a mass of algae, mainly Cyanophyta and green algae, bloom and form a thick layer of “green scum” on water surface. Algae can release toxins and render the organic matters in water to be decomposed into harmful gases, which will poison the fish and seashell.
The harmfulness of eutrophication also includes causing the shortage supply of drinking water source by degrading water quality. When the blooming algae die, they can produce lots of algae’s toxin which is harmful to human health. Cyanobacteria toxins (cyanotoxins) including cytotoxins and biotoxins are responsible for acute lethal, acute, chronic and sub-chronic poisonings of wild/domestic animals and humans. The biotoxins include the neurotoxins; anatoxin-a, anatoxin-a(s) and saxitoxins plus the hepatotoxins; microcystins, nodularins and cylindrospermopsins (Carmichael, 2001). Recent investigation showed that the algae produced toxins, which are the metabolized production of Cyanotoxins, were detected in the Yangtze River, as well as many reservoirs and lakes of Yellow River valleys, apart from Dianchi Lake, Taihu Lake and Chaohu Lakes (Yu and Len, 2004). Besides, increased nitrite concentration in the eutrophic water will be dangerous to human health, too, as products of nitrite nitrification process is a strong carcinogen. Thus, the exacerbation of water eutrophication with the increased severity of algae blooming in surface water system has attracted great attention of both public and private sections.
FACTORS INFLUENCING WATER EUTROPHICATION
Water eutrophication is mainly caused by excessive loading of nutrients into water bodies like N and P. Excessive nutrients come from both point pollution such as waste water from industry and municipal sewage, and non-point pollution like irrigation water, surface run water containing fertilizer from farmland, etc. Increased nutrient load to water body is now recognized as a major threat to the structure and functions of near shore coastal ecosystems, and severe eutrophication problems associated with harmful algal bloom is a major manifestation. Although related to nutrient enrichment in general, the basic cause of water eutrophication is more connected to an imbalance in the load of nitrogen and phosphorus with respect to silica (Dauvin et al., 2007). At present, excessive TN and TP in water are considered as the only factors inducing water eutrophication, but nutrient enrichment is only the necessary but not the sufficient condition for algal boom. Eutrophication is not likely to occur if both TN and TP in water are low, but eutrophication may not occur in water high in TN and TP if other conditions such as temperature and current speed are not favorable. The influencing factors of water eutrophication include: (1) excessive TN and TP, (2) slow current velocity, (3) adequate temperature and favorable other environmental factors, and (4) microbial activity and biodiversity (Li and Liao, 2002). Water eutrophication may occur rapidly when all of these conditions are favorable.
Nutrient enrichment
There is clear evidence that nutrient loading to lakes, estuaries and coastal oceans has greatly increased through human activities over the past few decades and that this has caused or enhanced many of the symptoms of the aquatic ecosystem transformation known as eutrophication (Bishop et al., 2006). There are different opinions on the relationship of nutrient enrichment to water eutrophication and algal bloom: (1) When P concentration in water is low, it may be the limiting factor for inducing water eutrophication and algal bloom; (2) When P concentration in water increases rapidly, other may become a new limiting factor, such as pH, water depth, temperature, light, wave, wind or other biological factors; (3) The influence of N and P still lasts for a longer time because of the high development level of our society (Zhao, 2004).
N and P input and enrichment in water are the most primary factors to induce water eutrophication. The “experienced molecular formula” of alga is as “C106H263O110N16P” based on the chemical components of algae. N and P are the two elements which account for least proportion in the molecular formula of algae, especially P, it is the main limiting factor to control the growth of alga in water (Mainstone and Parr, 2002). It was reported that 80% lake and reservoir eutrophication is restricted by phosphorus, about 10% lake and reservoir eutrophication is relative to nitrogen, and the rest 10% lake and reservoir eutrophication is relative to other factors (Zhao, 2004). In many ecosystems, phytoplankton biomass is correlated with the availability of N or P (Cloern 2001; Bledsoe et al., 2004). The composition of phytoplankton species is also affected by the concentrations of N and P (Reynolds, 2006). The ratio of N:P in the water body (referred to as the “Redfield ratio”) is an important indicator of which nutrient is limiting eutrophication. If the Redfield ratio is 16:1, P is most likely the limiting factor for algal growth; lower ratios indicate that N is of great importance (Redfield et al., 1963; Hodgkiss and Lu, 2004). P has been shown to be the principal limiting nutrient for primary production of phytoplankton in many freshwater environments (Phlips, 2002), while N is commonly limiting in marine ecosystems (Cloern, 2001). However, there are many exceptions to this general pattern. In some freshwater environments, particularly in the tropics and subtropics, N has been found to be the primary limiting nutrient for phytoplankton production, due in large part to excessive P load and long growing seasons. For instances, in the Ten Mile Creek of Indian River Lagoon, where TP is >0.2 mg/L, chlorophyll a and turbidity sharply increased with addition of available N (0.2~6.0 mg/L), but not affected by addition of reactive P (Lin et al., 2008). The results indicate that available N is the limiting nutrient for the growth of phytoplankton at water bodies with high P. In phosphate-deficient water bodies or those having reasonably good growth of blue-green algae, which fix enough of the atmospheric nitrogen, phosphorus becomes the limiting element, because a portion of P is used to counterbalance high nitrate content (Reynolds, 2006). Such circumstances can be seen that no paroxysmal algal boom may break out in heavily eutrophicated water bodies with both high N and P. Thus, it is the key point to control the concentrations of both N and P reasonably for solving the problem of water eutrophication.
The variations in the chemical composition of natural waters are believed to be an important factor in regulating the abundance, composition and geographical and periodic distribution of phytoplankton. It has been considered that the growth of phytoplankton is influenced by dissolved silicate-Si (DSi) concentration in water and its ratio to nitrate. When the DSi:nitrate-N atomic ratio is near 1:1, aquatic food webs leading from diatoms which require silicate to fish may be compromised and the frequency or size of harmful or noxious algal blooms may increase. Used together, the DSi:nitrate-N ratio and nitrate-N concentration are the robust comparative indicators of eutrophication in large rivers (Turner et al., 2003).
Hydrodynamics
There is no relationship between water disturbance and diatom alga occurrence or its scale, but water disturbing can influence the growth of Pyrrophyta alga because Pyrrophyta alga blooms when it is grown in relatively stable water. Cai et al.(2007) found that when there is no water to dilute, disturbing water itself can influence the process of eutrophication and species succession, which, however, is not related to disturbing water itself but is influenced indirectly by changing light and nutrient status. In shallow water, increased frequency of disturbance could increased the P release from the sediment, especially at high temperature (Cai et al., 2007). This is an instructional point to maintain beneficial alga in water. Also, tide not only can urge alga assembling but can also influence the multiplication of alga bloom through changing the concentration of nutrition in water. Zhu et al.(2007) studied the effects of hydrodynamics on phosphorus concentrations in water of Taihu Lake, a large, shallow and eutrophic lake of China. They found that hydrodynamical disturbance had no significant relationship with water quality at the top layer when significant wave height was smaller than 30 cm, but it significantly increased suspended solids (SS) concentration of the bottom water layer. Concentrations of nutrients showed no positive correlation with SS concentration in the water body. Intensive sediment resuspension may not have occurred when the hydrodynamic stress on sediment was only a little higher than the critical stress for sediment resuspension. A new method for confirming the critical stress for intensive sediment resuspension and nutrient release still needs to be developed. Le Pape and Menesguen (1997) studied hydrodynamic prevention of eutrophication in the Brest Bay (France). The Brest Bay is a semi-enclosed coastal ecosystem where primary production is nutrient-limited, even if huge nutrients loading from tributaries are present. The most striking feature of the bay is the semi-diurnal tidal influence, resulting in large water exchange with the continental shelf. A historical study of the available data has shown the steadiness of this ecosystem during the last two decades inspite of increasing eutrophic conditions.
Environmental factors
A range of factors are related to water eutrophication, but the mechanisms of their influencing algal bloom are not fully understood. In many moderately eutrophicated water bodies, algal bloom occurs in some seasons or some years, when the environmental conditions are favorable. The algal bloom caused by phosphorus inputs also modifies several abiotic factors of the water body. These factors directly govern the growth, diversity and density of the biotic components. The impact of algal bloom on any one or some of these factors indirectly influences the structure and characteristics of the water bodies. The influence of nutrient inputs on some of these factors is discussed as follows:
1. Temperature and salinity are the two important factors to induce alga bloom. Alga bloom always occurs at temperature between 23 °C and 28 °C, salinity between 23% and 28%. The variation of temperature and salinity also affect algal bloom, and an important condition for algal bloom is that temperature increases and salinity decreases faster than ever in short time. From the conception of ecology, exquisite change of temperature may cause the subrogation of biological communities, thus leading to algal bloom when other environment conditions are adequate (Wang et al., 1996). Statistical analysis shows that the influence of temperature on algal growth rate is the largest, followed by salinity and their interaction. The process of sporangium pullulating is hypersensitive to temperature. When under adequate temperature, it can bourgeon largely and alga bloom will form very fast. Change of salinity is also influenced by the concentration of nutrition. Research shows that salinity is negatively related with NO3 −-N, and PO4 3−-P, but positively related with NH4 +-N, and however, it is not very related with NO2 −-N. In addition, average temperature in winter is highly relative with the beginning growth time of Gymnodinium, but whether it has universality to all algae still needs to be studied. In the Vistula Lagoon, salinity gradient was determined as an important factor (along with water temperature and predation by young herring) that defined the dynamics of zooplankton abundance and biomass in this estuary (Telesh, 2004).
2. Carbon dioxide level is one of major factors controlling water eutrophication. Cyanophytes are more capable of utilizing low levels of carbon dioxide and become more buoyant at low levels of carbon dioxide and high pH. It keeps them in the upper layers of the water column with abundant sunlight. In addition, some species produce dense mats of vegetation, inhibit the growth of other phytoplankton, and also limit the swimming of zooplankton. These factors together mean that a slow-moving freshwater ecosystem can rapidly become dominated by blue-green algae, displacing not only members of the phytoplankton but some of the animal community as well. The reduction of light reaching the lake floor also inhibits submerged and rooted macrophytes, and sediments become anoxic as large amounts of planktonic biomass are added to them (Kant and Raina, 1990). The fluctuations in free carbon dioxide values correspond directly with the fluctuation in the standing crop of phytoplankton. As the diversity and density of phytoplanktons increase through various months, the amount of free carbon dioxide for photosynthetic activity becomes limiting. The pH changes in these ponds are governed by the amount of free carbon dioxide, carbon trioxide, and bicarbonate (Kant and Raina, 1990). Inflow nutrient concentration, inflow volume and inflow water temperature show very regular and reasonable impacts on the quality of lake water (Imteaz et al., 2003). Yin (2002) reported that monsoons served as a flushing mechanism in two ways: (1) They reduced seasonal eutrophication by nutrient enrichment in summer, and (2) they prevented long-term (annual) accumulation of organic matter in the sediments due to nutrient enrichment in the region. Because of the monsoon-influenced processes and low phosphorus in the Pearl River estuary, the estuary and adjacent coastal waters of Hong Kong appeared to be more resilient to enrichment of nitrogen.
3. Light plays an important role in the growth, diversity and density of aquatic flora. Algal growth has been reported to increase with light intensity, and luminescence of 4000 lux was found most favorable (Shen, 2002). As eutrophication progresses, a decline of submerged macrophytes occurs in many shallow water bodies, probably due to low light intensity caused by algal blooming. It is suggested that the adaptation strategy of Potamogeton maackianus under a certain range of low light stress is to accelerate the elongation of the main and lateral shoots and to increase their density (Ni et al., 1999). The light has been almost completely absorbed by the plankton of the top few meters, so that too little light penetrates to the thermocline and beyond to support photosynthesis. However, there is a rain of corpses into the deep water, whose decomposition requires oxygen. Since the deep water is cut off from the air until fall overturn, an oxygen deficit develops in the deep water, and the bottom mud is reduced. Eutrophication in an estuary is a complex process, and climate change is likely to affect each estuary differently due to interactions with nutrient loading and physical circulation. Hence, it is essential to consider the effects of climate change on the context of individual estuarine function to successfully manage eutrophication (Howarth et al., 2000).
There are other factors like pH and dissolved oxygen affecting water eutrophication (Khan and Ansari, 2005). The minima and maxima in the concentration of dissolved oxygen are found to be directly related to the maxima and minima of the phytoplankton, The direct relationship between phytoplankton and dissolved oxygen content has been observed by a number of researchers (Khan and Ansari, 2005). pH is a plant growth limiting factor. The change in pH is directly related to the availability and absorption of nutrients from solution. Ionization of electrolytes or the valence numbers of different ion species are influenced by changes in pH. An acidic pH has been reported to promote growth of Spirodelapolyrrhiza at a faster rate, but high pH values promote the growth of phytoplankton and result in bloom. It must be pointed out that many factors influencing eutrophication are relative and affect each other.
Microbial and biodiversity
Microbial activity is the inducement factor to alga bloom (Paerl, 1998; Paerl et al., 2003). It can enhance abundant breeding of alga bloom. Nutrient-enhanced microbial production of organic matter, or eutrophication, is frequently accompanied by altered microbial community structure and function (Paerl, 1998). The amount of microbial biomass is positively related to the content of organic matter and the amount of plankton in eutrophicated water. There exists certain intrinsic relationship between the amount of bacteria and the occurrence of eutrophication. The decomposition of organic matter by bacteria activities can produce nutrients and organic substances, which may promote algal bloom breaking out. Of course, it may also produce some toxic substances, which are harmful to other algal species, so that it will selectively enhance the bloom of some algae to become preponderant species and subsequently eutrophication will occur. It may be relative with the decomposing of bacteria biomass, which can promote effective circulation of nutrients when alga bloom and eutrophication occur under lower concentrations of nutrients. Chang et al.(2005) demonstrated that impose of submerged macrophyte in combination of immobilized nitrogen cycling bacteria could effectively reduce chlorophyll a concentration and increase water transparency. Marshland drainage channels (=ditches) in the UK are relicts of a once extensive habitat whose management requires quantitative information on the ecology of marshland organisms. Distribution of these organisms in wetlands worldwide can reflect natural water quality, vegetation and anthropogenic factors (Watson and Ormerod, 2004). Acrophyte-specific richness and abundance increased along an upstream-to-downstream zonation, which was characterized by an increase in mineralization and nutrient level (Thiébaut and Muller, 1998). In hyper-eutrophicated water body, remarkable improvement in water quality and inhibition on algal growth was obtained by introducing nutrient cycling bacteria in proper combination with floating hydrophyte (Chang et al., 2006).
A comparison of aquatic macrophyte diversity of two streams reflected the impact of human-induced perturbations (fish farms, domestic sewage) in such weakly mineralized and poorly buffered waters. Disturbed sites with very high nutrient loading were characterized by low vascular plant richness and by the absence of filamentous algae (Thiébaut and Muller, 1998). Vădineanu et al.(1992) studied the phytoplankton and submerged macrophytes in the aquatic ecosystems of the Danube Delta and found that the species changes were linked to accelerated eutrophication of the lakes, with increased phosphorus loading and a reduction in the N/P ratio. Distinct changes were observed in the macrophyte species composition in response to phosphorus enrichment (Vaithiyanathan and Richardson, 1999). Marshes in the unenriched and enriched areas were dominated by Ladiumjamaicense and Typha domingensis, respectively. Open-water areas were characterized by Eleocharis spp., Utricularia spp., Chara zeylanica and Nymphaea odorata in ligotrophic areas and by floating plants and Polygonum spp. in eutrophic areas. A shift in primary producers from eelgrass to macroalgae in response to increased nutrient loading altered the habitat, physicochemical structure and food webs. The nitrogen decreased shoot density and biomass of the eelgrass and promoted a record increase in the algal biomass (Deegan et al., 2002). Enhanced nutrient concentrations and loading have been observed in several coastal areas of the North Sea, resulting in increased production and changes in the species composition of phytoplankton (Colijn et al., 2002). Garg et al.(2002) studied aquatic flora in three lakes of Bhopal (Upper Lake, Lower Lake and Mansarovar Lake) in India and assessed the potential fertility of the lentic water and its aquatic flora. Eutrophication was highest in Mansarovar Lake. The observations of Garg et al.(2002) indicated that different species of phytoplankton could subsist up to a certain nutrient level, beyond which competition between cyanophytes and other algae enhanced and eliminated the sensitive plankton flora.
RESEARCH PERSPECTIVES
The problem of water eutrophication has become more and more severe worldwide, but the mechanism of its occurrence has not been fully understood. The limited knowledge of water eutrophication processes will add difficulties for the prevention and remediation of water eutrophication. Therefore, more researches should be turned to the mechanisms of water eutrophication under different watershed conditions. For example, the mechanisms of the adsorption and release of the contaminants in sediments should be clarified, which named inner pollution converging in water bodies, especially the absorption and release of P in sediments; the mechanism of the excessive production of algae and Cyanobacteria, especially excessive production of blue-green algae in water should be further studied, which is the key for the prevention of algae and Cyanobacteria growth. Also, the guidelines for estimating eutrophication are still very incomplete. Comprehensive guidelines for assessing eutrophication should be established by considering various factors in combination with the development of economy and society, especially in modern society ecology and health are paid more and more attention in order to avoid adverse influence on the sustainable ecological development and human health to the best of our abilities. In view of the high level of nutrients already polluted into lakes, reservoirs, estuaries, etc., understanding the functions of the factors influencing algal growth and bloom will certainly help controlling algal bloom even at high nutrient burden in surface water bodies.
Footnotes
Project supported by the Key Project from the Ministry of Education of China (No. 705824), the Project from Science and Technology Bureau of Zhejiang Province (No. 2006C13059), and a grant from the St. Lucie River Water Initiative (SFWMD contract No. OT060162), USA, in part
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