Available online at http://www.urpjournals.com International Journal of Research
in Fisheries and Aquaculture Universal Research Publications. All rights reserved
algal negative ecological consequenceson aquatic ecosystem chlorophyll, water transparency and dissolved structures, processes and functions,result in the fast growth oxygen. Although there are many different assessment of algae and otherplankton, and deteriorate water quality parameters, the concentrations of total nitrogen and (Western, 2001). Water eutrophication is caused by the phosphorus are the two basic ones (CNEPA, 2002).The autotrophic algae blooming in water,which composes its available parameters concerned include total nitrogen(TN), bioplasm by solar energy andinorganic substances through total phosphorus (TP), Chlorophyll-a, dissolvedoxygen photosynthesis. Inorganic nitrogen and phosphorus are the (DO), chemical oxygen demand by K2MnO 4 ox idation major control factors for the propagation of algae, method (COD Mn ), biological oxygen demand(BOD 5 especially phosphorus(Richardson et al., 2007). 3. Assessment of water eutrophication – Physical and Chemical evaluation Surface water quality guidelines have been improved in recent years.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), ), etc.(Cheng and Li, 2006). Table 2 shows the critical values of TN, TP, TNI and primary productivity in various eutrophicated water. It has been shown that theeutrophication or red/green 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 TP threshold concentration of 15 μg/L causes an ecological imbalance in algal, macrophyte and macro invertebrate community structure. Therefore it is considered that a buffering zone (12~15 μg/L) of TP may be more realistic and protective for all trophic levels. Table 1: Classification of surface water quality for lakes or reservoir (CNEPA, 2002) Items Surface water quality classification Class I Class II Class III Class IV Class V pH 6.0-7.0 7-7.5 7.5-8.0 8.0-8.5 8.5-9.0 DO (mg/L) Near saturation ≥6 ≥5 ≥3 ≥2 COD Mn (mg/L) ≤2 ≤4 ≤6 ≤10 ≤15 BOD 5 (mg/L) ≤3 ≤3 ≤4 ≤6 ≤10 TN (mg/L) ≤0.2 ≤0.5 ≤1 ≤1.5 ≤2 NH 3 -N (mg/L) ≤0.15 ≤0.5 ≤1 ≤1.5 ≤2.0 NO 2 -N (mg/L) ≤0.06 ≤0.1 ≤0.15 ≤1 ≤1 TP (mg/L) ≤0.01 ≤0.025 ≤0.05 ≤0.1 ≤0.2 Chlorophyll a ≤0.001 ≤0.004 ≤0.01 ≤0.03 ≤0.65 Transparency (m) ≥15 ≥4 ≥2.5 ≥1.5 ≥0.5 Escherichia coli (L−1) ≤200 ≤2000 ≤10000 ≤20000 ≤40000 DO: dissolved-oxygen; COD Mn : Chemical oxygen demand by K 2 MnO 4 oxidation method; BOD 5 : Biological oxygen demand; TN: Total nitrogen; TP: Total phosphorus. Table 2: Critical values of N and P in various eutrophicated water (Richardson et al., 2007) Eutrophic status TP (μg/L) TN (μg/L) Primary productivity (mg C/m2/day) Oligotrophic water 5-10 250-600 5-300 Mesotrophic water 10-30 500-1100 300-1000 Eutrophic water 30-100 1000-2000 >1000 Hypereutrophic water >100 >2000 >1000 3.1. Biological assessment of eutrophication – A new approach A set of ecological indicators including structural, functional and system-level aspects were proposed for a lake ecosystem health assessment according to the responses of lake ecosystems to chemical stresses like acidification, eutrophication, andcopper, oil and pesticide contamination. The structural indicators included phytoplankton cell size and biomass, zooplankton body size and biomass, speciesdiversity, macro- and micro- zooplankton biomass, thezooplankton/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 (Xuet al., 2001). 4. Influencing factors of 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 sources such as waste water from industry and municipal sewage and non- point pollution sources like irrigation water, surface run water containing fertilizer from farmland, etc. The basic cause of water eutrophication is more connected to an imbalance in the load of nitrogen and phosphorus with 171 International Journal of Research in Fisheries and Aquaculture 2013; 3(4): 170-175
respect to silica (Dauvinet al., 2007). At present, excessive TN and TP in water are considered as the only factors inducing water eutrophication. Rather, nutrient enrichment is only the necessary but not the sufficient condition for algal boom. Other influencing factors of water eutrophication include: slow current velocity, adequate temperature, other favorable environmental factors, microbial activity and biodiversity (Li and Liao, 2002). 4.1. Nutrient enrichment 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). The ―experienced molecular formula‖ of alga is as ―C algae. 106 H N 263 and O 110 P N are 16 P‖ the based two elements on the chemical which account components for least of proportion in the molecular formulaof 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, about10% 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 eutrophication. If the Redfield ratio is 16:1 or more, P is most likely the limiting factor for algal growth and 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. The variations in the chemical composition of natural waters are believed to be an important factor in regulating the abundance, composition, 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 (Turner et al., 2003). 4.2. Hydrodynamics There is no relationship between water disturbance and algal occurrence or its scale, but water disturbing can influence the growth periphytic algae because their blooms grow 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 is not related to disturbing water itself but is influenced indirectly by changing light and nutrient 172 International Journal of Research in Fisheries and Aquaculture 2013; 3(4): 170-175 status. In shallow water, increased frequency of disturbance could increase the P release from the sediment, especially at high temperatures (Cai et al., 2007). 4.3. Other environmental factors In many moderately eutrophicated water bodies, algal bloom occurs in some seasons or some years when the environmental conditions are favorable. The influence of some of these factors is discussed as follows: 4.3.1. Temperature Temperature induces alga bloom. Alga bloom always occurs at temperature between 23 °C and 28 °C. Statistical analysis shows that the influence of temperature on algal growth rate is the largest.The process of sporangium formation and bursting is hypersensitive to temperature. Under adequate temperature, it can propagate largely and alga bloom will form very fast (Wang et al., 1996). 4.3.2. Carbon dioxide Carbon dioxide level is one of major factors controlling water eutrophication. Cyanophytes are more capable of utilizing levels of carbon dioxide and become more buoyant at low levels of carbon dioxide and high pH. Some species produce dense mats of vegetation, inhibit the growth of other phytoplankton and also limit the swimming of zooplankton. 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). 4.3.3. Light 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 occur in many shallow water bodies, probably due to low light intensity caused by algal blooming.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 (Ni et al., 1999). 4.3.4. pH and Dissolved oxygen 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.High pH values promote the growth of phytoplankton and result in bloom
(Howarthet al.,2000). 4.4. Microbial biomass Microbial activity is the inducement factor toalga bloom (Paerl, 1998; Paerlet 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 bacterial activities can produce nutrients and organic substances, which may promote algal bloom (Watson and Ormerod, 2004). 5. Harmful effects of water eutrophication Water eutrophication disturbs the intrinsic equilibrium of the aquatic ecosystem and lead to the damage of the water ecosystem with gradual degeneration of its functions. As a result it can affect water quality and make transparency of water become worse. Thus little sunlight can penetrate water body and photosynthesis of plants under thewater will be weakened or even stopped. Water eutrophication can also cause the super-saturation or lack of dissolved oxygen in water, which will be stressful to aquatic animals and may cause death. Eutrophic systems tend to accumulate large amounts of organic carbon (Dell′Annoet al., 2002). Meanwhile due to water eutrophication, a mass of algae, mainly Cyanophyta and Chlorophyta, bloom and form a thick layer of ―green scum‖ on water surface. Algae can release toxins, consumes dissolved oxygen and render the organic matters in water to be decomposed into harmful gases, which will poison the fish/shellfish. The harmfulness of eutrophication also causes the shortage of drinking water source by degrading water quality. When the blooming algae die, they produce lots of algal toxin which is harmful to human health. Cyanobacterial toxins (cyanotoxins) include cytotoxins and biotoxins which are responsible for lethal, acute, chronic and sub-chronic poisonings of wild/domestic animals and humans. The biotoxins include the neurotoxins; anatoxins, saxitoxins, hepatotoxins, microcystins, nodularins and cylindrospermopsins (Carmichael, 2001). 6. Impact of eutrophication on the fisheries production of lentic systems – A contradictory case Eutrophication can cause problems such as bad tasteand odour in fishes captured from such waters. Sometimes it leads to the death of all forms of life in water bodies. On the other hand, it has also been reported that eutrophication increases the growth and age structure of planktivorous fish populations (ICAR, 2011).The increase in total catches incyprinid and silurid populations together with the decrease in percid, clupeid and salmonidis a well documented phenomenon in the eutrophic patches of rivers and reservoirs (Colby et al. 1972; Svärdson and Molin 1981; Persson et al. 1991). Organic matter depositing from the increased phytoplankton crops promotes oxygen consumption in the hypolimnion, causing even anaerobic conditions in lakes, reservoirs and tanks. A deoxygenated 173 International Journal of Research in Fisheries and Aquaculture 2013; 3(4): 170-175 hypolimnion excludes some fish groups such as percid, clupeid and salmonid, as they are intolerant of such situations. Fish tolerant of higher temperatures and lower oxygen concentrations may increase in production (Lappalainen, 1996). Usually in shallow lakes, dense algal growth out-competes the original aquatic plant beds. This means a loss of living habitats for young fish and a loss of spawning habitats for species that attach their eggs to aquatic plants. The abundance of large invertebrates living on plants, such as snails and insect nymphs, is also much curtailed, reducing the amount of suitable food for many larger carnivorous fishes. Such extreme conditions may be less favourable for cyprinids, too (Moss 1980).Changesin the physical environment induced by eutrophication such as decrease in submerged vegetation,increase in turbidity could affect thecompetitive interactions predator and prey, especially carnivorous fishes (Persson, 1983; Diehl, 1988). Cyprinids are able to feed efficiently at low light intensities and evenin darkness, whereas silurids, percids, clupeids and salmonids are visual hunters as they are dependent on vision (Diehl, 1988).Some highly eutrophic waterbodies also tend to produce large populations of stunted pan fish. This may be the result of inadequate predation onthese fish arising from the inability of predators to see them due to increased turbidity from planktonic algae and suspended sediment (Lee et. al., 2012). 7. Future suggestions The limited knowledge of water eutrophication processes will add difficulties for the prevention and remediation of water bodies. Therefore, more researches should be turned to the mechanisms of water eutrophication under different watershed conditions. References 1. Alongi, D.M., Chong, V.C., Dixon, P., Sasekumar, A., Tirendi, F., 2003. The influence of fish cage aquaculture on pe- lagic carbon flow and water chemistry in tidally domi- nated mangrove estuaries of peninsular Malaysia. Marine Environmental Research, 55(4):313-333. 2. Andersen, J.H., Conley, D.J., Hedal, S., 2004. Palaeoecology, reference conditions and classification of ecological status: The EU Water Framework Directive in practice. Marine Pollution Bulletin, 49(4):283-290. 3. Bledsoe, E.L., Phlips, E.J., Jett, C.E., Donnelly, K.A., 2004. The relationships among 336 phytoplankton biomass, nutrient loading and hydrodynamics in an inner-shelf estuary. Ophelia, 58(1):29-47. 4. Cai, J.B., Ding, X.F., Peng, H.Y., Chang, H.Q., Yang, X.E., 2007. Effects of environmental factors and submerged aquatic plants on phosphorus release from the sediment. Journal of Soil and Water Conservation, 21(2):151-154. 5. Carmichael, W.W., 2001. Health effects of toxin- producing Cyanobacteria: ―The CyanoHABs‖. Human and Ecological Risk Assessment, 7(5):1393-1407. 6. Cheng, X.Y., Li, S.J., 2006. An analysis on the evolvement processes of Lake Eutrophication and their characteristics of the typical lakes in the middle and lower reaches of Yangtze River. Chinese Science
Bulletin, 51(13): 1603-1613. 7. CNEPA (Environmental Protection Agency of China), 2002. Environmental Quality Standard 8. Cloern, J.E., 2001. Our evolving conceptual modle of the coastal eutrophication 350 problem. Marine Ecology Progress Series, 210:223-253. 9. Colby, P.J., Spangler, G.R., Hurley, D.A. and McCombie, A.M. 1972. Effects of eutrophication on salmonid communitiesof oligotrophic lakes. J. Fish. Res. Board Can.29: 975–983. 10. Dauvin, J.C., Ruellet, T., Desroy, N., Janson, A.L., 2007. The ecological quality status of the Bay of Seine and the Seine estuary: Use of biotic indices. Marine Pollution Bulletin, 55(1-6):241-257. 11. Dell′Anno, A., Mei, M.L., Pusceddu, A., Danovaro, R., 2002. Assessing the trophic state and eutrophication of coastal marine systems: A new approach based on the bio- chemical composition of sediment organic matter. Marine Pollution Bulletin, 44(7):611-622. 12. Diehl, S. 1988. Foraging efficiency of three freshwater fishes: effects of structural complexity and light. Oikos53: 207–214. 13. Fang, Y.Y., Yang, X.E., Pu, P.M., Chang, H.Q., Ding, X.F., 2004. Water eutrophiocation in Li-Yang Reservoir and its ecological remediation countermeasures. Journal of Soil and Water Conservation, 18(6):183-186. 14. Hodgkiss, I.J., Lu, S.H., 2004. The effects of nutrients and their ratios on phytoplankton aboundance in Junk Bay, Hong Kong. Hydrobiologia, 512(1-3):215-229. 15. Howarth, R.W., Swaney, D.P., Butler, T.J., Marino, R., 2000. Climatic control on eutrophication of the Hudson River estuary. Ecosystems, 3(2):210-215. 16. ICAR. 2011. Handbook of fisheries and aquaculture. ICAR publication, New Delhi. 17. Kant, S., Raina, A.K., 1990. Limnological studies of two ponds in Jammu. II. Physico-chemical parameters. Journal of Environmental Biology, 11(2):137-144. 18. Khan, F.A., Ansari, A.A., 2005. Eutrophication: An ecological vision. The Botanical Review, 71(4):449- 482. 19. Lappalainen, A. and Pönni, J. 1996. The Gulf of Finland in the fisherman‘s eyes - Pollution and recreational fishery in the Gulf of Finland. Finnish Game and FisheriesResearch Institute, Helsinki. Kalatutkimuksia 107. 44pp. 20. Lee, G. F. and Jones, R. A. 1991. ̳Effects of Eutrophication on Fisheries‘, Reviews in Aquatic Sciences, CRC Press, Boca Raton, FL 5:287-305. 21. Li, J.X., Liao, W.G., 2002. Discussion on the synthetic adjustive guidelines for the prevention and cure of eutrophication. Protection of Water Resource, 2(5):4-5. 22. Liu, W., Qiu, R.L., 2007. Water eutrophication in China and the combating strategies. Journal of Chemical Technol- ogy and Biotechnology, 82(9):781- 786. 23. Mainstone, C.P., Parr, W., 2002. Phosphorus in rivers- ecology and management. The Science of the Total Environment, 282-283(1-3):25-47. 24. Moss, B. 1980. Ecology of fresh waters. Man and medium. Blackwell Scientific Publications, Oxford. 332 pp. 25. Ni, L.Y., Wang, D.M., Xie, P., 1999. Experimental Studies on the Growth of Potamogetonmacckianus A. under Low-Light Stress in Highly Eutrophic Water. Acta Hydrobiologica Sinica, 23:53-58. 26. Paerl, H.W., 1998. Structure and function of anthropogenically altered microbial communities in coastal waters. Current Opinion in Microbiology, 1(3):296-302. 27. Paerl, H.W., Dyble, J., Moisander, P.H., Noble, R.T., Piehler M.F., Pinckney, J.L., Steppe, T.F., Twomey, L., Valdes, L.M., 2003. Microbial indicators of aquatic ecosystem change: current applications to eutrophication studies. FEMS Microbiology Ecology, 46(3):233-246. 28. Persson, L. 1983. Effects of intra- and interspecific competitionon dynamics and structure of a perch Percafluviatilis and a roach Rutilusrutilus population. Oikos41: 197–207. 29. Persson, L., Diehl, S., Johansson, L., Andersson, G. andHamrin, S. 1991. Shifts in fish communities along theproductivity gradient in temperate lakes — patterns andthe importance of size-structured interactions. J. FishBiol. 38: 281–293. 30. Phlips, E.J., 2002. Algae and Eutrophication. In: Bitton, G. (Ed.), Encyclopedia of Environmental Microbiology. John Wiley and Sons, New York. 31. Redfield, A.C., Ketchum, B.H., Richards, F.A., 1963. The Influence of Organisms on the Composition of Seawater. In: Hill, M.N. (Ed.), The Sea. Volume 2. Wiley-Interscience, New York, p.26-77. 32. Reynolds, C., 2006. Ecology of Phytoplankton. Cambridge University Press, Cambridge, p.535. 33. Richardson, C.J., King, R.S., Qian, S.S., Vaithiyanathan, P., Qualls, R.G., Stow, C.A., 2007. Estimating ecological thresholds for phosphorus in the Everglades. Environ- mental Science and Technology, 41(23):8084-8091. 34. Shen, D.S., 2002. Study on limiting factors of water eutro-phication of the network of rivers in plain. Journal of Zhejiang University (Agriculture and Life Sciences), 28(4):94-97. 35. Svärdson, G. and Molin, G. 1981. The impact of eutrophication and climate on a warmwater fish community. Rep.Inst. Freshw. Res., Drottningholm 59: 142–151. 36. Tong, C.H., Yang, X.E., Pu, P.M., 2003. Degradation of aquatic ecosystem in the catchment of Mu-Ge Lake and its Remediation countermeasures. Journal of Soil and Water Conservation, 17(1):72-88. 37. Turner, R.E., Rabalais, N.N., Justic, D., Dortch, Q., 2003.Global patterns of dissolved N, P and Si in large rivers.Biogeochemistry, 64(3):297-317. 38. Wang, Z.F., Zhang, Q., Lu, Y., Lv, H.Y., 1996. The effects of nutrients and trace metals on the growth of the red tide organism Prorocentrummicans. Donghai Marine Sci- ences, 14(3):33-38. 39. Watson, A.M., Ormerod, S.J., 2004. The distribution of three uncommon freshwater gastropods in the 174 International Journal of Research in Fisheries and Aquaculture 2013; 3(4): 170-175
drainage ditches of British grazing marshes. Aquatic Conservation, 118(3): 455-466. 40. Western, D., 2001. Human-modified ecosystems and future evolution. Proceedings of the National Academy 41. of Sci- ences of the United States of America, 98(10):5458-5465. 42. Xu, F.L., Tao, S., Dawson, R.W., Li, P.G., Cao, J., 2001. Lake ecosystem health assessment: Indicators and methods. Water Research, 35(13):3157-3167. 43. Zhao, S.C., 2004. Mechanisms of Lake Eutrophication and technologies for controlling in China. Advance in Earth Sciences, 19(1):138-140.
Source of support: Nil; Conflict of interest: None declared
175 International Journal of Research in Fisheries and Aquaculture 2013; 3(4): 170-175