AGRICULTURE AND BIOLOGY JOURNAL OF NORTH AMERICA ISSN Print: 2151-7517, ISSN Online: 2151-7525, doi:10.5251/abjna.2011.2.1.56.60 © 2011, ScienceHuβ, http://www.scihub.org/ABJNA Health implications of harmful algal blooms in tank culture of catfish Agatha A. Nwabueze Department of Fisheries, Delta State University, Abraka, Asaba, Campus, Asaba, Nigeria, E-mail: [email protected] ABSTRACT Health implications of harmful algal bloom in tank culture of Clarias gariepinus were investigated to ascertain its possible effects on fish by application of commonly used organic manure for pond fertilization. Poultry droppings, cow dung and excess feeding were used to generate algal blooms in tanks A, B and C respectively with tanks held in a static non-renewal bioassay and tank D (control) in static renewal bioassay. Ten juvenile cat fish introduced into the tanks were fed twice daily. Water samples were collected weekly from all tanks and analyzed by microscopy for presence of algae and water quality parameters. Algal bloom was observed in tanks A and B while blooms were not found in Tanks C and D. Algal species identified were Anabaena, Volvox, Phacus, Euglena, Spirogyra, Chlamydomonas, Synedra, Mallomones, Oscillatoria, Ceratium, Dinoflagellates, Cladophora, and Microcystis. Similar species with significantly higher (P≥ 0.05) number of algae/ ml was observed in tanks A and B than in C and D. The duo of Anabaena and Chlamydomonas blooms had the highest number of algae/ ml in tanks A and B respectively. Fish kills and algae die off were observed in tanks A and B as well as oxygen depletion also in tank C except in control. Dissolved oxygen level was significantly reduced (P ≥0.05) in tanks A and B when compared tanks C and D. Turbidity levels followed an increasing sequence of tanks D < C < A < B. Temperature and pH in treatment tanks were not significantly different from control. This study has shown that using poultry droppings for pond fertilization can encourage harmful algal bloom. There is a need to assess and monitor algal growth in tank culture of fish to know the species of algae in water samples and be able to estimate the algal density which is important to reduce impact of algal bloom in water bodies. Keywords: Health implications, harmful algal bloom, tank culture, catfish. INTRODUCTION Algae are naturally occurring microscopic plants that are usually aquatic, unicellular and lack true stems, roots and leaves (Bowman et al., 2010). Algae are a diverse group of simple, typically autotrophic organisms ranging from unicellular to multi cellular forms (Wikipedia, 2010). Algae are natural fish food and its density determines the greenness of pond water and primary productivity (Alphonse, 1997). An algal bloom is a rapid increase or accumulation in the number of algal cells such that the algae dominate the planktonic community (Bowman et al., 2010). According to Lathrop et al. (1998) and Diersing (2009), fresh water algal bloom results from excessive nutrients, particularly phosphorus, which originates from fertilizers that are applied to land for agricultural or recreational purposes and enter watersheds through run-off. Additional causes of algal bloom have been documented (Anderson et al., 2002). Problems associated with algal bloom include algae die off which lead to oxygen depletion of water column (hypoxia or anoxia) from cellular respiration and bacterial degradation (Mellergaard and Nielson, 1987). Chorus and Bartram (1999) also noted that when algae die off and decompose, carbon dioxide and nutrients are released back into the pond for the next generation of plants. Harmful algal bloom can occur when certain types of microscopic algae grow quickly in water forming visible patches. This often times, may contain cyanobacteria because most species of algae are not harmful and serve as the energy producers at the base of the food web (Falk et al. 2000). Cyanobacteria, also known as blue-green algae are actually bacteria, not algae, since their genetic material is not organized in a membranebound nucleus as found in true algae which have true nucleus (Agriculture & Agri-food, 2007). However, algae and cyanobacteria occur together naturally in surface waters where both can undergo blooms. Blue-green algae have been identified as having ability to produce highly potent toxins referred to as cyanotoxins (Anderson et al., 2000). Anderson et al (2006) observed that harmful algal bloom constitute serious threat to coastal resources, causing impacts ranging from contamination of sea food products with potent toxins to mortalities of wild and farmed fish and other marine animals. Other problems Agric. Biol. J. N. Am., 2011, 2(1): 56-60 associated with algal blooms are objectionable odor and tastes, poor aesthetic value, large fluctuation in pH, clogging of fish gills leading to fish kill, poisoning of fish, livestock and humans who drink or bath in ponds with algal bloom. The original weight of the oven-dried filter paper which was obtained before filtration was subtracted from the weight of the desiccated filter paper plus samples. The value obtained was taken as the value of suspended solids in the sample. Turbidity was determined using a secchi disk. Algae were collected by horizontal tows with a 55µm-1 mesh size bolting silk plankton net at a depth of 25 cm according to APHA (1992). Samples were preserved in 4% formalin. Samples were decanted to remove the supernatant. Fresh clean water was added to the sediment and centrifuged. The supernatant was again decanted and fresh water added to make up to 10 ml in the centrifuge tube which was agitated and 1 ml of subsample pipette onto the counting chamber (Neubauer haemacytometer, Marienfeld) for quantitative estimation of species of algae by examining fractions of each sample under the microscope. Algae were identified to generic level as much as possible and enumerated by binocular microscopy (x 100 magnification) using keys according to Willoughby (1976) and Green Water/Cyano Laboratories (2007). The number of algae/ml was calculated according to a formula by Boyd and Lichtkoppler (1979). Rearing of catfish in tank is rapidly developing in Nigeria and poultry dropping is commonly used as manure for fertilization. However, many interested fish farmers lack the basic knowledge of algal bloom and its application in tank culture of fish. To maintain productivity of tank culture, algal density must be monitored within favorable ranges and species of algae identified to prevent algal blooms, particularly harmful blooms which may be deleterious to fish health and by implication, health of fish consumers. This study investigates the health implications of harmful algal blooms in tank culture of catfish. MATERIALS AND METHODS The study which lasted six months in 2008 was conducted in the Department of Fisheries, Delta State University, Abraka, Asaba Campus. Four experimental concrete tanks measuring 6ft x 4ft x 4ft were used. Each tank contained borehole water to 2.5ft level. Two jute sacs of four kg each of poultry droppings and cow dung as well as excess feeds were used to generate algal bloom in tanks A, B and C respectively in the culture of Clarias gariepinus, catfish held in static non-renewal bioassay systems. Tank C received excess feeds while the fourth (tank D) was held in a static renewal bioassay and served as the control. All four tanks were allowed to stand for two weeks before the introduction of ten juvenile C. gariepinus (averaging 18.4 + 0.05 cm, total length and 133.1 + 0.14 g, weight) in each of the tanks. Supplementary feeding of fish in all four tanks was carried out twice daily (10.00 am and 6.00 pm) with commercially available feeds at 4% body weight for eight weeks. The experiment was replicated twice of eight weeks each. Water samples from the four tanks were collected weekly and analysis. Temperature was determined in-situ with mercury –in-glass thermometer. Dissolved oxygen was determined by oxygen meter (LabTech., England) while pH was determined using an electric pH model PHS-25 (Techmel and Techmel, USA) pH meter. The meter was standardized with solution of known pH and meter adjusted accordingly before use. For total suspended solids, gravimetric method was used. Briefly, 100 ml of water samples were filtered through dried weighted Whatman no.4 filter paper. The filter 0 was oven-dried at a temperature of 105 C and stored in a desiccator until a constant weight was obtained. Number of plankton (algae)/ml = T x 1000 AN x Vol. of concentrate in ml/Vol. of sample Where: T = total number of algae counted A = area of grid in mm2 N = number of grid counted 1000 = area of counting chamber in mm2 Skin scrapings of samples of catfish in each tank were examined by microscopy for presence of algae. Data obtained were subjected to analysis of variance (ANOVA) at P≤0.05 level of significance. While the significant means were separated with the Duncan’s multiple range test (DMRT) using SAS (1996). RESULTS Algal bloom was observed in experimental tanks A and B with poultry droppings and cow dung organic manure respectively. Algae without bloom were found in Tanks C and D (Control). Algal species identified were Anabaena, Volvox, Phacus, Euglena, Spirogyra, Chlamydomonas, Synedra, Mallomones, Oscillatoria, Ceratium, Dinoflagellates, Cladophora, and Microcystis colony. There was also unidentified plankton in some of the samples. Table 1 shows algae species found in the treatment and control tanks. Similar species with high number of algae/ ml were found in tank culture with poultry droppings and cow dung. This was significantly higher (P≥ 0.05) 57 Agric. Biol. J. N. Am., 2011, 2(1): 56-60 than species and number of algae/ ml in tanks C and D (Control). Blooms in Anabaena followed by Chlamydomonas species of algae were observed. The duo having the highest number of algae/ ml in tanks with poultry droppings and cow dung manure. The number of Anabaena was higher in poultry droppings while Chlamydomonas was higher in cow dung manure. A progressive increase in algal number was observed in all tanks during the study. Mean weekly abundance of algae species/ ml in the culture tanks are presented in tables 2 and 3.Objectionable odor was perceived from tanks A and B which also had fish kills. Three (33.3%) and two (20%) of ten fish each in tanks A and B respectively were found th th floating on water surface in the 6 and 7 weeks of the study. Some fish samples in tanks A and B also had their gills clogged with green scum of algae some of which were found floating on the surface of the tank water. The skin of some of the fish samples examined had patches of greenish algae. Algae die off were observed on the surface around the inside walls of tanks A and B. Skin scrapings from fish samples shows the presence of algal cells on the skin surface. Analysis of water quality parameters shows that oxygen depletion occurred in the non-renewal static bioassay tanks A, B and C while tank D with renewal bioassay system had higher levels of oxygen. Dissolved oxygen level was significantly reduced (P ≥0.05) in tanks A and B with poultry droppings and cow dung manure but not significantly reduced (P≤ 0.05) in tank C when compared with the control. Water turbidity was highest in the cow dung treatment tank B. Turbidity levels followed an increasing sequence of tanks D (control) < C < A < B .Turbidity levels were however not significantly higher (P ≤ 0.05) in tanks A and B than in tanks C and D. Secchi disk depth measurement shows that tank B had a depth of 0.06m, followed by tank A with 0.11m, tank C, 0.29m and tank D, 0.58m. A mean pH value of 8.2 and 8.7 was observed in tanks A and B respectively while pH in tank C had a mean of 7.2 and in tank D it was 6.8. Temperature remained fairly 0 0 constant with 29.4 C to 29.9 C range. Table 4 shows the mean values of water quality parameters determined. of study. The growth of algae was faster in the tank with poultry droppings than the tank with cow dung. Ajayi (2006) noted that poultry droppings generated the most productive algal blooms. Blooms of Anabaena found in tank A with poultry droppings and Chlamydomonas in tank B with cow dung show a possibility of harmful algal bloom, especially in fish culture using poultry droppings for pond fertilization. Wikipedia (2010), reported that only one or few species of phytoplankton algae are normally involved in blooms. Anabaena and Chlamydomonas had the highest growth in number/ml among thirteen algal species found in water samples. According to Anderson (1997) a great variety of algae species can be found in water samples with algal bloom some of which may be harmful. The algal species found include blue-green algae (cyanobacteria) such as Anabaena, Microcystis and Oscillatoria. These bluegreen algae especially Anabaena have been reported to be capable of causing negative impacts to other organisms via production of natural potent toxins. Health Link (2005) reported that blue-green algae can be poisonous if swallowed in water by wildlife, livestock and humans. Although toxicity testing of harmful algal bloom was not done, the occurrence of harmful algal bloom in one of the treatment tanks is enough reason to be cautious in the application and use of organic manure in tank culture of systems. Agriculture and Agri- Food (2007) reported that it is difficult to a certain when blue-green algae bloom produce toxins and so it is better to avoid them completely. Treatment tanks A and B had objectionable odor probably arising from the manure used and the presence of algae which contribute distinctive odors and tastes to water such as Anabaena, Volvox, Mallomones, Synedra and Ceratium (Haine et al., 2001). Fish gills were observed to be clogged with scum of algae from tank surface water. Skin scrapings also showed presence of algal cells on fish. The clogging of fish gills may have resulted in obstruction of gaseous exchange coupled with low level of oxygen in the tanks due to the algae die off and subsequent bacteria degradation. These facts probably contributed to the fish kill observed in the sixth and seventh week of the experiment. Algae die off have been reported to increase organic matter in the water necessitating degradation by aerobic bacteria which further depletes the oxygen content of the water. Oxygen depletion alone has also been known to be capable of causing fish kill (Connell and Miller, 1984). DISCUSSION Algal bloom observed in experimental tanks with poultry droppings and cow dung organic manure is an evidence of excess nutrients in the tanks. The growth of algae was not delayed as results obtained showed a progressive algal growth during the period 58 Agric. Biol. J. N. Am., 2011, 2(1): 56-60 Table 1: Algal species in treatment and control tanks. S/No Tank A Tank B Poultry Droppings Cow Dung Tank C (Excess Feed) Tank D (Control) 1 Anabaena Anabaena 2 3 4 Volvox Phacus Euglena Volvox Phacus Euglena Volvox Euglena Euglena 5 6 7 Spirogyra Chlamydomonas Synedra Spirogyra Chlamydomonas Synedra Spirogyra Chlamydomonas - Spirogyra Chlamydomonas - 8 9 10 Mallomones Oscillatoria Ceratium Mallomones Oscillatoria Ceratium Oscillatoria Ceratium 11 12 13 Dinoflagellate Cladophora Microcystis Dinoflagellate Cladophora Microcystis Dinoflagellate Cladophora - - - Cladophora - Source: Field survey (2008). Table 2: Mean weekly abundance of algae species in treatment tanks. S/No Algae Species Week 1 Week 2 Week 3 Week 4 Week 6 Week 7 Week 8 1 Anabaena 2.7 3.0 3.2 4.5 6.1 7.8 8.3 8.6 5.5 2 3 Volvox Phacus 2.1 2.0 2.3 2.5 2.8 2.9 3.3 3.0 3.7 3.3 4.0 4.6 4.9 4.8 5.5 5.6 3.6 3.6 4 Euglena 2.3 2.6 2.8 3.1 3.4 5.0 5.1 5.3 3.7 5 Spirogyra 2.4 2.5 3.0 3.2 3.5 4.2 4.7 5.2 3.6 6 Chlamydomonas 3.0 3.2 3.3 4.2 5.8 6.4 7.3 8.1 5.2 7 8 Synedra Mallomones 2.6 2.3 2.7 2.6 2.9 2.8 3.4 2.9 4.1 3.3 4.5 3.7 4.9 4.0 5.2 4.4 3.8 3.3 9 Oscillatoria 1.9 2.2 2.4 2.5 2.8 3.0 3.6 3.8 2.8 10 Ceratium 1.6 1.8 2.1 2.5 3.1 3.4 3.6 4.0 2.8 11 Dinoflagellate 2.0 2.7 2.8 2.9 3.0 3.2 3.5 3.9 3.0 12 13 Cladophora Microcystis 1.8 2.0 2.4 2.2 2.7 2.5 3.0 2.6 3.5 2.9 3.6 3.6 3.8 4.1 4.2 4.2 3.1 3.0 Source: Field survey Week 5 Total (2008). Table 3. Mean weekly abundance of algae species in control tank. S/No Algae Species Week 1 Week 2 Week 3 Week 4 Week 5 Week 6 1 Euglena 1.2 1.4 1.5 1.7 2.0 2.3 2 Spirogyra 1.5 1.8 2.1 2.2 2.4 2.6 3 Chlamydomonas 1.4 1.7 1.8 1.9 2.3 2.4 4 Cladophora 1.3 1.3 1.6 1.8 1.9 2.0 Source: Field survey (2008). Table 4: Mean values of water quality parameters in treatment and control tanks. S/No Water Quality Parameter Tank A Tank B (poultry droppings) (Cow dung) 1. Dissolved oxygen (mg/l) 2.2 2.7 2. Turbidity (secchi 0.11 0.06 Depth, m) 3. pH 8.7 8.2 4. Temperature(0C) 29.9 29.4 5. Suspended solids(mg/l) 112.6 101.3 Source: Field survey (2008). 59 Week 7 2.5 2.7 2.6 2.2 Week 8 2.8 2.9 2.7 2.4 Tank C (excess feed) 3.1 0.29 7.2 29.8 94.5 Total 1.9 2.3 2.1 1.8 Tank D (control) 4.4 0.58 6.8 29.6 67.7 Agric. Biol. J. N. Am., 2011, 2(1): 56-60 The water samples analyzed clearly showed that there was oxygen depletion in tanks A and B. Tank C also had reduced oxygen content probably due to the nonrenewal bioassay system, which did not provide for improvement in the oxygen content of the tank water. Tank D with renewal of bioassay system however, had oxygen content with optimal ranges for fish growth. Turbidity levels were higher in the treatment tanks than in the control. The greenish color impacted in the tank water by the algal bloom is likely responsible for the higher turbidity observed in the treatment tanks. Similar reports also show that greenness of the algal bloom signifies density of algae or high algal turbidity (Alphonse, 1997). High algal turbidity has been reported to reduce the penetration of sunlight into water bodies (NLWRA, 2008). Increased levels of pH observed corroborate earlier studies of Radke (2008), who noted that photosynthetic consumption of CO2,especially in algal bloom causes an increase in the level of pH. Pollution Control Federation Washington, DC. 14th edition. New York. 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