A comparative study of zooplankton diversity and abundance from
Transcription
A comparative study of zooplankton diversity and abundance from
2nd International Conference on Agriculture, Environment and Biological Sciences (ICAEBS'15) August 16-17, 2015 Bali (Indonesia) A comparative study of zooplankton diversity and abundance from three different types of water body Azma Hanim Ismail, and Siti Azrin Zaidin sites with aim of contributing to the knowledge of zooplankton diversity in Malaysian water bodies. Abstract—In this study, we compared the species composition and diversity of planktonic Rotifera, Cladocera and Copepoda between river, irrigation canal and rice field ecosystem in Balik Pulau, Penang, Malaysia. The present study was carried out from October 2013 to February 2014. Average total diversity of zooplankton tended to be the highest in river (24 species) and the lowest in rice field (19 species). Despite the relatively high species number of zooplankton supported by river, irrigation canal water body seems to contribute considerably higher total abundance than the other two types of ecosystem. Data analysis highlighted significant difference in zooplankton abundance among the different types of water body (p = 0.004). The zooplankton abundance was influenced by physical factors of the water bodies. Correlation analysis revealed a strong positive relationship between zooplankton abundance and water transparency (r = +0.547), while there exists a weak negative correlation with dissolved oxygen (r = -0.238) and temperature (r = -0.234). The findings of the present study provide useful knowledge on the spatial organization of zooplankton diversity in different types of freshwater ecosystem as well as can be used as management strategies to protect the aquatic biodiversity in the agricultural area. Keywords— Rotifera, Cladocera, Copepoda, II. MATERIALS AND METHODS A. Study Site Balik Pulau is a suburban area on the southwest part of Penang Island. The present study was carried out in three types of freshwater ecosystems in Balik Pulau which were river, irrigation canal and rice field. Five stations were established (Fig. 1) and the characteristics of each station are shown in Table I. Malaysia, zooplankton. I. INTRODUCTION Zooplankton are microscopic animals that act as primary and secondary links in the food webs of all aquatic ecosystems. They feed on phytoplankton which directly provide food source for larval vertebrates and invertebrates as well as related to the growth of juvenile and larger fish. They are also important component in the transfer of energy from primary producers of phytoplankton to higher trophic levels such as fish [1]. Regarding the habitat, zooplankton are cosmopolitan fauna and inhabit all freshwater bodies of the world [2]. These communities are also sensitive to various substances in water such as nutrient enrichment and pollutants. Thus, they have often been used as indicators to assess the condition and change of the freshwater environment particularly in the northern hemisphere [3]. The present study has been undertaken to determine the zooplankton diversity and abundance in relation to physical parameters in the study Fig. 1 Study area with sampling stations of irrigation canal, rice field and Burung River in Balik Pulau, Penang. Azma Hanim Ismail, Universiti Sains Malaysia, Malaysia, Siti Azrin Zaidin, Universiti Sains Malaysia, Malaysia http://dx.doi.org/10.17758/IAAST.A0715053 37 2nd International Conference on Agriculture, Environment and Biological Sciences (ICAEBS'15) August 16-17, 2015 Bali (Indonesia) TABLE I CHARACTERISTICS OF SAMPLING STATIONS IN BALIK PULAU, PENANG Station Ecosystem Mean depth (m) 1 Irrigation canal 0.65 2 Irrigation canal 0.55 3 Rice field 0.15 4 Burung River 1.05 5 Burung River 1.48 taxonomic level according to the standard taxonomic references [4], [5] and [6]. Geographic coordinates 5°2007.62 N, 100°1241.33 E 5°2019.08 N, 100°1244.33 E 5°2015.11 N, 100°1241.79 E 5°2034.20 N, 100°1246.19 E 5°2033.75 N, 100°1247.36 E C. Data Analyses In order to provide more information on zooplankton community dynamic, some ecological indices were calculated which were diversity indices (Simpson Index and ShanonWiener Index), richness indices (Margalef Index and Menhinick Index) and evenness index (Pielou Index) according to [7]. All of the data has been compiled into Microsoft Excel spreadsheet based on sampling stations and sampling months. Normality test was performed using SPSS to determine whether the input data is normally distributed. Since the data was not normally distributed, non-parametric analysis of Kruskal-Wallis was performed in order to see if there is any difference on zooplankton species number and abundance between sampling stations. Spearman correlation was used to describe the degree of relationship [8] between zooplankton abundance and physical parameters. The result can show how strongly pairs of variables such as temperature, pH, dissolved oxygen and water transparency are related to zooplankton abundance. Spearman correlation was performed and the range of values was between +1 to – 1. When the coefficient, r exceed 0.5, thus it indicates that the correlation is strong. B. Data Collection Field sampling was conducted monthly from October 2013 until February 2014 for 5 months. Zooplankton samples were collected by filtering 40 L of water through a Wisconsin conical plankton net (35 µm mesh size). Samples were transferred into 120 ml screw cap plastic container and preserved with 70% ethanol before transported to the laboratory. Three sample replicates were collected for each station to increase accuracy of the result. Station 3 dried out during the sampling occasion so it present fewer samples compared to the other stations. In - situ parameters including dissolved oxygen (DO), temperature and pH were measured at the surface water of all sampling stations. Dissolved oxygen (DO) (mg/L) and temperature (°C) were measured using a YSI meter (Model 57), while pH was measured using the Orion pH meter (Model 230A). Water transparency was measured using Secchi disc. The disc was lowered slowly into the water until it was disappeared from eyesight. The depth at which the pattern on disc is no longer visible was recorded. Water depth was measured using scaled rope attached with a weight at the end of the rope. Then, it was lowered into the water until reached the bottom. The depth was taken as a measure of water depth. In the laboratory, three sub-sample of 1 mL for each replicate were examined under a compound microscope (Olympus BX40) at various magnifications using a SedgwickRafter counting cell. In order to ensure that the plankton was fairly distributed, sample bottle has been shaken before introducing into the cell. 1 ml of well mixed sub-sample was filled into the cells using an adjustable volume pipette. Then cover slip was placed gently to avoid any air bubbles trapped in the cell. Sample was allowed to settle for at least 10 minutes to ensure that zooplankton was settled into a single layer. These steps were repeated three times for each sample bottle and an average of the counts was recorded. The organisms were expressed as individual per liter (ind/L) of the sample. Zooplankton abundance was derived from the following formula: Individu / L = AC / L III. RESULTS A. Zooplankton Diversity A checklist of zooplankton species occurred in the study sites are shown in Table II. B. Zooplankton Abundance Zooplankton abundance throughout the study period is shown in Fig. 2. The highest zooplankton abundance (182 ind/L) was recorded in the month of November 2013 while the lowest abundance (19 ind/L)) was noticed in the month of February 2014. All zooplankton groups occurred at the highest abundance in November 2013 while the lowest in February 2014 which was dominated by Rotifera, followed by Copepoda and Cladocera. Fig. 3 shows the percentage of zooplankton abundance at each station during the study period. Rotifera shows the highest abundance at all sampling stations compared to the other groups. The highest abundance of Rotifera occurred at Station 5 (145 ind/L), Copepoda at Station 2 (12 ind/L), while Copepoda at Station 3 (9 ind/L). Based on result of KruskallWallis test, there was a statistically significant difference in zooplankton abundance between sampling stations (p = 0.004). C. Physical Parameters Dissolved oxygen, temperature, pH and water transparency were measured while collecting zooplankton samples. Their mean and standard error values are given in Table III. Where, A = Average number of individual per mL; C = Volume of concentrated sample in mL; L = Volume of filtered water in L Zooplankton were identified and enumerated at the lowest http://dx.doi.org/10.17758/IAAST.A0715053 38 2nd International Conference on Agriculture, Environment and Biological Sciences (ICAEBS'15) August 16-17, 2015 Bali (Indonesia) TABLE II ZOOPLANKTON SPECIES CHECKLIST AND DISTRIBUTION BY SAMPLING STATION DURING THE STUDY PERIOD (OCTOBER 2013 UNTIL FEBRUARY 2014) ORDER 1 2 STATION 3 4 5 Branchionus angularis Branchionus nilsoni Branchionus forficula Branchionus quadridentatus Keratella cochlearis Anuraeopsis sp. Plationus patulus Lepadella sp. Colurella uncinata Dicranophoroides sp. Asplanchna sp. Lecane bulla Lecane hamata Lecane lateralis Lecane luna Lecane papuana Lecane cf. ungulata Lophocharis sp. Notommata sp. Proalides sp. Scaridium sp. Conochillus sp. Filinia sp. Testudinella sp. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + Diaphanosoma sarsi Diaphanosoma sp. + - + - + + - - Adult Nauplii + + + + + + + + + FAMILY SPECIES ROTIFERA Branchionidae Lepadellidae Ploimida Flosculariacea Bdelloidea CLADOCERA Diplostraca Dicranophoridae Asplanchnidae Lecanidae Mytilinidae Notommatidae Proalidae Scaridiidae Conochilidae Filinidae Testudinellidae Sidiidae COPEPODA Cyclopoida Fig. 2 Different groups of zooplankton abundance during the study period http://dx.doi.org/10.17758/IAAST.A0715053 Fig. 3 Different groups of zooplankton abundance at all sampling stations during the study period 39 2nd International Conference on Agriculture, Environment and Biological Sciences (ICAEBS'15) August 16-17, 2015 Bali (Indonesia) Zooplankton abundance was strong positively correlated with water transparency (r = 0.547) while negative correlations were found with dissolved oxygen (r = -0.238) and temperature (r = -0.234). Correlations of zooplankton abundance with physical parameters in the study sites are given by Table IV. TABLE III MEAN VALUES (MEAN ± SE) OF PHYSICAL PARAMETERS IN ALL SAMPLING STATIONS 4.92 ± 0.30 Temperature (°C) 27.82 ± 0.24 7.12 ± 0.11 Water transparency (m) 0.55 ± 0.06 5.24 ± 0.30 28.33 ± 0.33 7.12 ± 0.11 0.57 ± 0.06 3 3.42 ± 0.70 28.00 ± 0.31 7.28 ± 0.23 0.15 ± 0.02 4 3.44 ± 0.42 28.05 ± 0.38 5.79 ± 0.24 0.82 ± 0.04 5 4.16 ± 0.33 28.11 ± 0.26 6.26 ± 0.29 0.82 ± 0.07 Station DO (mg/L) 1 2 pH D. Ecological Indices Table V shows the ecological indices at all sampling stations during the study period. The highest value of Margalef TABLE IV SPEARMAN CORRELATION VALUES OF ZOOPLANKTON ABUNDANCE AND PHYSICAL PARAMETERS DURING THE STUDY PERIOD Zooplankton DO Temperature pH Transparency 1.000 Zooplankton -0.238* 1.000 DO -0.234* 0.037 1.000 Temperature 0.076 0.407** -0.067 1.000 pH 0.547** -0.199 -0.415** -0.382** 1.000 Transparency *. Correlation is significant at the 0.05 level (2-tailed). **. Correlation is significant at the 0.01 level (2-tailed). Station 1 2 3 4 5 TABLE V ECOLOGICAL INDICES AT ALL SAMPLING STATIONS DURING THE STUDY PERIOD Richness indices Diversity Indices Eveness indices Menhinick Margalef (R1) Simpson (D) Shannon-Wiener (H’) Pielou (J) (R2) 5.46 2.50 0.83 1.09 0.76 4.27 2.02 0.85 1.07 0.81 4.79 2.90 0.93 1.20 0.94 5.60 2.65 0.90 1.21 0.84 5.15 2.16 0.88 1.17 0.82 The number of zooplankton species recorded in rice field ecosystem of present study was lower than that reported in references [17] and [18]. However, reference [19] reported lower species number of zooplankton compared to Burung River in the present study. The differences of species number among the studies probably due to the differences in terms of sampling frequency, sampling methods and physical parameters measurements during the sampling periods. In the present study, zooplankton abundance was strong positively correlated with water transparency. This is good evidence that an increase in the water transparency leads to an increase in the zooplankton communities [12]. The Simpson index in the present study shows high values (0.83 - 0.93) which indicated that the communities are mature and stable as the dominance is shared by large number of species. Low diversity which is usually showed close to zero values is a signal that the communities are under stress conditions [20]. The Pielou index values which are more than 0.5 indicated that the zooplankton ecology is balance during the study period. If the values are less than 0.5, it could be an indicator of the presence of ecological stress with the occurrence of few dominant species at high density in the study site [21]. index occurred at Station 4 (5.60) while the lowest value found at Station 2 (4.27). Menhinick index showed the highest value of richness at Station 3 (2.90) while the lowest value was at Station 2 (2.02). The values of diversity index of Simpson index varied from 0.83 to 0.93 while the values for ShanonWiener index fluctuated between 1.07 and 1.21. Pielou’s Evenness index showed the highest value of 0.94 at Station 3 while the lowest value was recorded at Station 1 for 0.76. IV. DISCUSSION The present study showed that rotifers dominated all three types of water body in terms of species richness and abundance. This finding is in accord with work by [9] and [10], who reported that rotifers are the dominant group in their study sites. The high number of rotifers in freshwater ecosystem is due to their less specialized feeding habits, high fecundity and short developmental rates [11]. In fact, this pattern is common in freshwater ecosystem such as lakes, ponds, rivers and streams [12]. Cladocera and Copepoda were observed in lower species richness and abundance compared to Rotifera. This is due to the effects of size-selective predation by fish [13] and the changes in chemical characteristics of the water condition [14]. In terms of copepods, the abundance of nauplii was always higher than the adult stages [15]. This is probably due to the larger size of adult forms which increase the predation intensity compared to juvenile forms [16]. http://dx.doi.org/10.17758/IAAST.A0715053 V. CONCLUSION The qualitative analysis of zooplankton from all three aquatic ecosystems revealed the presence of three taxonomic groups: Rotifera, Cladocera and Copepoda. From those, 40 2nd International Conference on Agriculture, Environment and Biological Sciences (ICAEBS'15) August 16-17, 2015 Bali (Indonesia) [15] H. Y. Zakaria, A. A. Radwan and M. A. Said, “Influence of salinity variations on zooplankton community in El-Mex Bay, Alexandria, Egypt,” Egypt. J. Aquat. Res. vol. 33, no. 3, pp. 52–67, 2007. [16] E. V. Sampaio, O. Rocha, T. Matsumura-Tundisi and J. G. Tundisi, “Composition and abundance of Zooplankton in the limnetic zone of seven reservoirs of the Paranapanema River, Brazil,” Braz. J. Biol. vol. 62, pp. 525–545, 2002. http://dx.doi.org/10.1590/S1519-69842002000300018 [17] A. B. Ali, “Seasonal dynamics of microcrustacean and rotifers communities in Malaysian ricefields used for rice-fish farming,” Hydrobiologia, vol. 206, pp. 139-148, 1990. http://dx.doi.org/10.1007/BF00018640 [18] A. S.R.M. Shah and A. Ali, “Distribution and seasonal dynamics of zooplankton in the Muda rice agro-ecosystem,” in Sustainable rice production in Malaysia beyond 2000, M. Nashriyah, S. Ismail, N. K. Ho, A. Ali, K. Y. Lum and M. Mashhor, Eds. Malaysia: Malaysia Institute for Nuclear Technology (MINT) and Muda Agricultural Development Authority (MADA), 2002, pp. 285. [19] N.Z. Zulikha, F.M. Yusoff, J. Nishikawa, A. Arshad and H.M. MatiasPeralta, “Mesozooplankton composition and abundance in a tropical estuary during monsoon season,” Journal of Fisheries and Aquatic Science. vol 8, pp. 430-440, 2013. http://dx.doi.org/10.3923/jfas.2013.430.440 [20] M. C. Dash, Fundamental of Ecology. New Delhi: Tata McGraw-Hill, 2003, pp. 516-527. [21] S. M. Frutos, A. S. Poi de Neiff and G. Neiff, “Zooplankton abundance and species diversity in two lakes with different trophic states (Corrientes, Argentina),” Acta Limnol. Bras. vol. 21, no. 3, pp. 367– 375, 2009. rotifers are best represented as number of species diversity and abundance, followed by cladocerans and copepods in nauplius, copepodite and adult froms. The dominance of zooplankton species is highly variable in different types of water body according to nutrient levels, predator and other environmental factors which then affects the other biotic components of the ecosystems. ACKNOWLEDGMENT This research project was supported by funds from Universiti Sains Malaysia (grant no. 1001/PBIOLOGI/811243). The authors are grateful to Dr. Russell Shiel for helping with the identification of zooplankton. REFERENCES [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] R.S. Stemberger, “An inventory of rotifer species diversity of northern Michigan inland Lakes,” Archiv für Hydrobiologie. vol. 118, pp. 283302, 1990. S. K. Mukhopadhyay, B. Chattopadhyay, A. R. Goswami and A. Chatterjee, “Spatial variations in zooplankton diversity in waters contaminated with composite effluents,” J. Limnol. vol. 66, pp. 97-106, 2007. http://dx.doi.org/10.4081/jlimnol.2007.97 D. Rissik, D. van Senden, M. Doherty, T. Ingleton, P. Ajani, L. Bowling, M. Gibbs, M. Gladstone M, T. Kobayashi, I. Suthers and W. Froneman, “'Plankton-related environmental and water-quality issues,” in Plankton, a guide to their ecology and monitoring for water quality, 1st ed. I.M. Suthers, D. Rissik, Eds. Melbourne: CSIRO Publishing, 2009, pp. 39–72. R. W. Pennak, Freshwater invertebrates of the United States. New York: John Wiley & Sons, Inc., 1978, pp. 1-803. B. A. G. Idris, Freshwater zooplankton of Malaysia (Crustacea: Cladocera). Malaysia: Universiti Pertanian Malaysia, Serdang, Selangor, 1983, pp. 10-151. R. J. Shiel, A guide to identification of rotifers, cladocerans and copepods from Australian inland waters. Albury: Co-operative Research Centre for Freshwater Ecology, Murray-Darling Freshwater Research Centre, 1995, pp. 1-142. E. Ogbeigbu, Biostatistics, a practical approach to research and data handling. Nigeria: Minex publishing Company Limited, Benin City Nigeria, 2005, pp. 153-155. J. H. Zar, Biostatistical analysis. New Jersey: Prentice Hall, Upper Saddle River, 1999, pp. 395-398. W. Reckendorfer, H. Keckeis, G. Winkler and F. Schiemer, “Zooplankton abundance in the River Danube, Austria: the significance of inshore retention. Freshwater Biol. vol. 41, pp. 583–591, 1999. http://dx.doi.org/10.1046/j.1365-2427.1999.00412.x A. M. Rabee, “The effect of Al-Tharthar – Euphrates Canal on the quantitative and qualitative composition of zooplankton in Euphrates River,” J. Al-Nahrain Univ. vol. 13, no. 3, pp. 120–128, 2010. J. D. Allan, “Life history patterns in zooplankton,” American Naturalist., vol. 110, pp. 165–176, 1976. http://dx.doi.org/10.1086/283056 I. F. Neves, D. Rocha, K. F. Roche and A. A. Pinto, “Zooplankton community structure of two marginal lake of river (Cuiaba) (Mato, Grosso, Brazil) with analysis of rotifer and Cladocera diversity,” Braz. J. Biol., vol. 63, no. 2, pp. 329–343, 2003. http://dx.doi.org/10.1590/S1519-69842003000200018 J. F. Pankow, Aquatic Chemistry Concepts. Chelsea: Lewis Publishers, 1991, pp. 109–127. E.S.F. Medeiros, and A.H. Arthington, “The importance of zooplankton in the diets of three native fish species in floodplain waterholes of a dryland river, the Macintyre River, Australia,”.Hydrobiologia, vol. 614, pp. 19– 31, 2008. http://dx.doi.org/10.1007/s10750-008-9533-7 http://dx.doi.org/10.17758/IAAST.A0715053 About Author: Spatial organization of zooplankton community will contribute to the knowledge of zooplankton diversity in Malaysian water bodies. 41