• google scholor
  • Views: 7485

  • PDF Downloads: 312

Insect diversity and water quality parameters of two ponds of Chatla wetland, Barak valley, Assam

Pinki Purkayastha1 and Susmita Gupta1 *

1 Department of Ecology and Environmental Science, Assam University, Silchar, 788 011 India

DOI: http://dx.doi.org/10.12944/CWE.7.2.08

An investigation was carried out on two ponds of Chatla floodplain, Barak valley, Assam with special reference to aquatic insects.  Pond 1 is purely a fish pond where as pond 2 is a community pond too.  Present study revealed the status of water quality and in turn diversity, density, dominance and abundance of aquatic insects in both the ponds. Almost all the physico chemical parameters of both the ponds were found within permissible range for aquatic life .However in pond 2 level of phosphate was found little higher than pond 1 due to release of soaps and detergents by human influence. In both the ponds order Hemiptera showed maximum relative abundance ( 98% in pond 1 and 94% in pond 2).  The study revealed lower diversity of aquatic insects in pond 2  than that in pond 1.

Chatla Floodplain; Pond; Human Interference; Water Quality; Aquatic Insects

Copy the following to cite this article:

Purkayastha P, Gupta S. Insect Diversity and Water Quality Parameters of Two Ponds of Chatla Wetland, Barak Valley, Assam. Curr World Environ 2012;7(2):243-250 DOI:http://dx.doi.org/10.12944/CWE.7.2.08

Copy the following to cite this URL:

Purkayastha P, Gupta S. Insect Diversity and Water Quality Parameters of Two Ponds of Chatla Wetland, Barak Valley, Assam. Curr World Environ 2012;7(2):243-250. Available from: http://www.cwejournal.org/?p=2814


Download article (pdf)
Citation Manager
Publish History


Article Publishing History

Received: 2012-07-12
Accepted: 2012-09-17

Introduction 

Among different ecosystems, wetlands constitute one of the most important ecosystems for man offering numerous regulating services. Water quality assessment of small water bodies of the wetlands are of immense importance in the management of fisheries, water supply, and irrigation. Pollution status of water bodies are usually expressed as biological and physico-chemical parameters.1 Several authors have extensively documented the responses of macro-invertebrates to organic and inorganic pollution.2,3 Chatla floodplain (24042/697// N and 92046/264//E) situated in the south of Silchar town, Barak Valley, Assam has 1500 fishery ponds and 12 seasonal lakes. (Fig.1). Although the wetland is resourceful with variety of macrophytes, trees and fishes it is in a derelict or near derelict state due to high rates of siltation, infestation of weeds, unscientific fishing activities, and  use of pesticides in the surrounding tea gardens and  agricultural fields 4 which led to a loss of  73% wetland area of Chatla floodplain.5  All these factors can affect the communities of aquatic organisms leading to loss of diversity and species extinction.6 Since, fluctuations in aquatic insect community can give quick information of their surrounding water quality and are commonly used as tools for marking an integrated assessment of water quality, investigation on water quality of two fishery ponds of Chatla wetland with special reference to aquatic insects was carried out.

Material and Methods

The topography of the Chatla floodplain is fenland type with small hillocks strewn among large stretches of lowland.  Pond 1 is a fish pond and is relatively undisturbed. Pond 2 is a fishery cum community pond. Water and insect samples were collected in replicates from both the sites during 2009-2010. Physico-chemical parameters such as Air temperature (AT), Water temperature (WT), Transparency, pH, Electrical Conductivity (EC), Dissolved oxygen (DO), Free CO2 , Total alkalinity (TA), Nitrate (NO3-) and Phosphate (PO4 3-), Nitrite (NO2-), and Ammonium (NH4 +) content of water were analyzed by standard methods.7,8 The aquatic insects were collected by kick method whereby the vegetation was disturbed and the circular net (mesh size 60µm) was dragged around the vegetation for one minute.9,10 They were immediately sorted, preserved in 70% ethyl alcohol and were later identified using Dewinter advanced stereo zoom microscope with the help of standard keys.11,12,13,14,15,16,17 A number of identified insects were confirmed in the entomological laboratory of Zoological Survey of India. Statistical analyses were done by MS EXCEL 2007; SPSS 15.0 for Windows, Shannon Wiener Index of Diversity (H/ ), Evenness Index (J/) and Berger–Parker Index of  Dominance (d)  were calculated by Biodiversity professional version 2 for windows.

Result and Discussion

Different physico-chemical parameters (AT, WT, Transparency, pH, EC, DO, Free CO2,TA, PO4 3-, NO3 -, NO2 -, NH4 +)  in pond 1 and 2 during Post monsoon 2009 to Monsoon 2010  and their mean concentrations are shown in Table 1. Table 2 showed the distribution of aquatic insects in pond 1 and 2. The significant correlations that exist among environmental variables, diversity and density of insect are shown in Table 3. Fig.2 showed the relative abundance of aquatic insect orders recorded from pond 1 and pond 2 during the study period. Relative abundance of aquatic insect families and aquatic insect species in pond 1 and 2 are shown in the Fig.3 and Fig.4 respectively.  Pattern of variation in the levels of Shannon –Weiner Diversity index (H') and Evenness index (J') and Berger-Parker index of Dominance (d) are shown in the Fig.5.The study revealed that in pond 1 and 2 both air and water temperature did not show much variation. In pond 1 DO, EC, NH4 and NO3 -concentration were slightly higher than that of pond 2 while other parameters such as Transparency, Free CO2, TA, pH, and PO4 3-concentration were recorded to be higher in pond 2. The solubility and availability of nutrients is affected by oxygen content of water and therefore the productivity of aquatic ecosystems.18 The range of DO recorded in the present study is similar to the DO concentration reported in a previous study in the same area.19 In pond 1 correlation coefficient analyses revealed a significant negative relationship of WT with pH and DO. Classical negative relationship of WT with DO was also recorded in a previous study on Chatla floodplain20 which is attributed to the fact that in lower temperature oxygen carrying capacity of water increases.21 Negative relationship of DO with Rainfall might be an indication that surface runoff transported sewage, fertilizer etc. into the pond which have lowered DO value by bacterial respiration.22 EC was found to be higher in pond 1 (4.59ms/ppt ± 2.93) compared to pond 2 ( 3.24ms/ppt ± 0.20) where it showed significant positive correlation with TA and NO3-. The range  of NO3-. between 0.1 - 3.0   mgl-1 is considered favorable for fish productivity.23 In both the ponds, NO3-. concentration was found within the said range indicating their suitability for fish production.  In pond 2 EC showed significant positive correlation with TA, Free CO2, and DO. Higher free CO2 accompanied by higher TA and higher pH in pond 2 could be due to external application of lime. It is known that addition of lime increases fish production in soft (low total hardness) waters by stabilizing the pH of bottom mud and increasing the availability of Phosphorus and Carbon dioxide for photosynthesis. The overall effect of liming is to increase phytoplankton production which results in increased fish production.24 Another reason might be that in heavily stocked fish ponds, Carbon dioxide (CO2) concentration can become high as a result of respiration. High CO2 concentrations are almost always accompanied by low DO concentrations (high respiration). Acidity of rain water has impact on the pH of natural water bodies. As rain falls to the earth, each droplet becomes saturated with CO2 and pH is lowered.25 This explained the negative relationship of Rainfall with pH in pond 1. However in pond 2 no such relationship could be found due to application of lime. In pond 1 DO has shown significant positive correlation with pH , such type of positive correlation in between DO and pH have been recorded from the study of Asa lake llorin , Nigeria26 where DO distribution followed a similar annual cycle with the pH. In pond 2 DO has shown a positive significant correlation with TA. These alkalinity relationships are extremely important in water chemistry, since the most prominent water problems are deposits and corrosion, and these are closely related to the instability of each  specific water caused by the tendency of CaCO3 to dissolve in or precipitate from it.27 Range of PO43- (0.86 ± 0.27  in pond 1 and 1.25 ± 0.72 in pond 2) recorded in the present study is  supported by the previous study in a marsh of the same floodplain.28 Relatively high concentration of PO43- in pond 2 might be due to its use as community pond where PO43- is contributed by household activities such as washing, bathing etc. In pond 1 PO43- has shown significant positive correlation with NO3 -. Actually large concentration of PO43- and NO3 - reported together from a water body indicate  that water is eutrophic in nature 29 but  as the water of this pond showed low concentration of both ,it indicates the water is not eutrophicated. Rainfall showed significant negative relationship with NO3 - and positive correlation with NO2- in pond 2. A previous study conducted in the same study area also reported relatively high concentration of NO3 - during dry months.30 A positive correlation between NO2- and NH4+ is supported by the fact that the most possible way of Nitrate entry in an aquatic system is through oxidation of Ammonia form of Nitrogen to NO2-   and to NO3 - consequently.31
 
Table 1: Physico-chemical properties of water of Pond 1 and Pond 2 Table 1: Physico-chemical properties of
water of Pond 1 and Pond 2

Click here to View table
 
Table 2: Distribution of aquatic insect species in Ponds 1 and 2 of Chatla floodplain during study period Table 2: Distribution of aquatic insect species in
Ponds 1 and 2 of Chatla floodplain during study period

Click here to View table
 
Table 3: Significant Correlations among environmental variables, diversity and density of aquatic insects for pond 1 and pond 2 Table 3: Significant Correlations among environmental variables, diversity and density of aquatic insects
for pond 1 and pond 2

Click here to View table
 
 Fig. 1: Location of the two Ponds , 1 and 2 in the floodplain of Chatla Wetland Figure 1: Location of the two Ponds , 1 and 2 in the
floodplain of Chatla Wetland

Click here to View figure
 
 Fig. 2: Relative abundance of insect orders in Pond 1 and Pond 2 Figure 2: Relative abundance of insect
orders in Pond 1 and Pond 2

Click here to View figure
 
 Fig. 3: Relative abundance of aquatic insect families in Pond 1 and Pond 2 Figure 3: Relative abundance of aquatic insect
families in Pond 1 and Pond 2

Click here to View figure

Aquatic insect community of pond 1 was represented by two orders- Hemiptera, Odonata; four families- Gerridae, Notonectidae, Mesoveliidae (Hemiptera), Coenagrionidae (Odonata) and seven species. Pond 2 was represented by three orders Hemiptera, Odonata, Diptera; five families- Notonectidae, Gerridae, Mesoveliidae (Hemiptera), Coenagrionidae (Odonata); Culicidae (Diptera) and seven species (Table 2). In both the ponds order Hemiptera was the most prominent order, having 98% relative abundance in pond 1 and 94% in pond 2. The most abundant family in Pond 1 is Notonectidae (64%), followed by Gerridae (32%), Mesoveliidae (2%), and Coenagrionidae (2%). In Pond 2 the relative abundance of Gerridae was highest (76%) followed by Notonectidae (16%), Coenagrionidae (5%), Mesoveliidae (2%) and Culicidae (1%) (Fig.2 and 3). The aquatic insect species found common in both the ponds were Gerris lepcha Distant, Limnogonus nitidus Mayr, Enithares fusca Brooks, Mesovelia vittigera Horvath, Enallagma sp. and Anisops barbata Brooks. In addition to these species Neogerris parvula Stål was recorded in pond 1 and Culex sp. in pond 2 (Fig.4).  Values of Shannon –Weiner Diversity index (H') and Evenness index  (J')  were found higher in pond 1 than that of Pond 2  while  Berger-Parker index of Dominance (d)  value was  found higher in pond 2 (Fig. 5).  However the H’ values were found to be less than 1 in both the ponds indicating polluted nature of water 32 . In pond 1 insect density has shown negative correlations with PO43- and NO2-. This might be due to the reason that increased pollution level with high concentration of PO43- and NO2-.might have disturbed the colonization as many species of aquatic insects are very susceptible to pollution or alteration of their habitat 33.  In pond 2 density of aquatic insects showed positive correlation with Free CO2 which might be due to increased respiration by more number of insects. Rainfall 34 has shown no significant relationship with diversity or density of aquatic insects in both the ponds. The diversity of aquatic insects showed positive correlation with Transparency. Such kind of positive correlation was reported from lake Victoria 35. From the study, it can be said that different physico chemical parameters of water quality are inter related and these factors influence diversity, density and distribution of aquatic insects in a particular water body.
 
Fig. 4: Relative abundance of aquatic insect species in Pond 1 and Pond 2 Figure 4: Relative abundance of aquatic insect
species in Pond 1 and Pond 2

Click here to View figure
 
Fig. 5: Pattern of variation in the levels of Shannon diversity index, Evenness index and Berger-Parker dominance of different insect species in both the Ponds Figure 5: Pattern of variation in the levels of Shannon
diversity index, Evenness index and Berger-Parker dominance of different insect species in both the Ponds

Click here to View figure

Acknowledgements

The authors are thankful to University Grants Commission, New Delhi, India for financial support. Authors are also thankful to the Head, Department of Ecology and Environmental Science, Assam University, Silchar, Assam for providing laboratory facilities.

References
 
  1. Lenat,  D.R. , Smock, L.A .  and Penrose, D.L., Use of Benthic Macroinvertebrates as Indicators of Environmental Quality, Biological Monitoring for Environmental Effects, Lexinton Books, Toronto,  Canada, p-7-114 (1980).
  2. Thorne,  R.S.T.J. and  Williams, W.P. , The response of benthic macroinvertebrates to pollution in developing countries: a multimetric system of bioassessment, Freshwater Biol., 37, 671-686  (1997). http://dx.doi.org/10.1046/j.1365-2427.1997.00181.x
  3. Kazanci, N. and Dugel , M., Ordination and classification of macro invertebrates  and   environmental data of stream in Turkey, Water Sci. Tech., 47, 7-8 (2000).
  4. Laskar H. S. and Gupta, S., Chatla Wetland, Cachar, Assam: An ecological appraisal, Northeast Researches, 3(2), 39-48 (2011).
  5. Phukon, P. and  Laskar , A.A., Wetland Mapping and Change Detection in Part of Barak Valley Using Remote Sensing and GIS, Map India, (2006).
  6. Primack, R.B. and Rodrigues ,  E., Biologia da Conservação, Londrina ( Edited by Viva), p-328  (2001)  .
  7. Michael, P., Ecological Methods for Field and Laboratory Investigations, Tata Mc. Graw-Hill publishing Company Ltd., New Delhi , p-434 (1984).
  8. APHA, Standard methods for the Examination of Water and Wastewater, 19th edition,  Published by American Public Health association, 1015, fifteen streets NW Washington, D.C. 20 R.C.0015 ( 2005).
  9. K.C. Gupta and J. Oberai, Orient J. Chem., 26(1): 215-221 (2010).
  10. A. Malviya, S.K. Diwakar, Sunanda, O.N. Choubey, Orient. J. Chem., 26(1): 319-323 (2010).
  11. Brittain,  J.E., Studies on the lentic Ephimeroptera and Plecoptera of Southern Norway, Norskent. Tidsskr , 21, 135-151 (1974).
  12. Subramanian, K.A. and  Sivaramakrishnan , K.G., Aquatic insects for biomonitoring fresh water ecosystems: A methodology manual, Trust for Ecology  and Environment (ATREE) , Bangalore, India, p-31(2007).
  13. Kumar, A., Description of the last instar larvae of Odonata from Dehra Dun Valley (India) with notes on biology. I. Suborder Zygoptera, Oriental Insects, 7, 83-118 (1973a). http://dx.doi.org/10.1080/00305316.1973.10434207
  14. Kumar, A., Description of the last instar larvae of Odonata from Dehra Dun Valley (India) with notes on biology. II. Suborder Anisoptera, Oriental Insects, 7, 291-331(1973b). http://dx.doi.org/10.1080/00305316.1973.10434222
  15. Thirumalai, G., Aquatic and semi aquatic hemiptera (Insecta) of Javadi Hills, Tamilnadu, Zool. Surv. of India, 18, 63 (1989).
  16. Thirumalai, G., Aquatic and semi aquatic hemiptera (Insecta) of Tamilnadu-1,Dharampuri and Pudukkatai districts, Zool.Surv.India, Occasion 165,45 (1994).
  17. Bal, A. and  Basu , R.C., Insecta: Hemiptera: Mesovellidae, Hydrometridae, Veliidae  and Gerridae, In: State fauna series 5, Fauna of West Bengal, India, p-511-534(1994 a).
  18. Westfall , M.J. Jr. and Tennessen , K.J., Odonata, In: An introduction to the aquatic insects of North America, (Edited by Merritt , R. W. and Cummins, K. W. ) , Dubuque , Kendall Hunt Publishing, IA3,p-164-169 (1996) .
  19. ZSI,  State fauna series 10. Fauna of Manipur, (Part -2) Insects, Zoological Survey of India, Kolkata, India (2004).
  20. Wetzel, R.G., Detrial dissolved and particulate organic carbon functions in aquatic ecosystems, Bulletin of Marine Science, 33,503-509 (1984).
  21. Bhuiyan,  J.R. and  Gupta, S.A., Comparative Hydrobiological Study of a Few Ponds of Barak Valley, Assam, and Their Role as Sustainable Water Resources, J.  Environmental Biol., 28(4),  799-802 (2007).
  22. Laskar, H.S. and Gupta, S., Phytoplankton diversity and dynamics of Chatla floodplain lake, Barak Valley, Assam, North East India – A seasonal study, J  Environmental Biol. 30 (6), 1007-1012 (2009).
  23. Wetzel, R.G., Limnology, 2nd edn., Philadelphia :Saunders Coll. Publication, p-860 (1983).
  24. Singhal, R.N., S, and Davies , R.W. ,The physicochemical environment and the plankton of managed ponds in Haryana, India, Proc Ind Acd Ani  Sci.,  95, 353-364 (1986). http://dx.doi.org/10.1007/BF03179369
  25. Verma, S.K. , Fresh water toxic blue-green algal blooms - A response to extra nutrient enrichment,  In: Ecology of polluted waters (Edited  by Kumar , A.). Voll. II, A.P.H. Publishing Corporation, New Delhi,  1161-1175 (2002).
  26. Lewis, G.W., Pond Fertilization and Liming. Cooperative Extension Service, University of Georgia College of Agricultural & Environmental Sciences, Athens (1998).
  27. William, A.W. and Durborow. , M.R., Interactions of pH, Carbon Dioxide, Alkalinity and Hardness in Fish Ponds, SRAC Publication No. 464 (1992).
  28. Araoye, P.A., The seasonal variation of pH and dissolved oxygen (DO2) concentration in Asa lake Ilorin, Nigeria, Int. J. of Physical Sciences, 4(5), 271-274 (2009).
  29. www.onlinewatertreatment.com (Technifax).
  30. Laskar, H.S. and Gupta,  S., Ecology of a marsh in Chatla floodplain, Barak Valley,North-East India,  Ecology  Environment & Conserv.,16(3), 333-339(2010).
  31. Ahmad, U., Parveen, S. Khan , A.A. ,  Kabir , H.A. , Mola , H.R.A.  and Ganai, A.H., Zooplankton population in relation to physico-chemical factors of a sewage fed pond of Aligarh (UP), India, Biology and Med. 3(1), 336-341(2011).
  32. Duttagupta,  S., Gupta S. and  Gupta, A., Gupta Euglenoid blooms in the floodplain wetlands of Barak Valley, Assam, North Eastern India, J Environmental Biol., 25, 369-373(2004).
  33. Rajasegar,  M. , Psysico-Chemical Characteristics of the Vellar estuary in relation to shrimp farming,  J  Environmental Biol., 24, 95-101(2003).
  34. Staub, R., Appling,  J.W. , Hofsteiler , A.M. and Hass, I.J., The effect of industrial wastes of Memphis and Shelby county on primary plankton producers,  Bioscience, 20, 905-912 (1970). http://dx.doi.org/10.2307/1295583
  35. Voshell, J.R. Jr. ,A Guide to Common Freshwater Invertebrates of North America, McDonald & Woodward Publishing Company,Granville, Ohio, p-.442 (2002).
  36. Cachar College Meteorological Observatory data , Cachar College, Silchar , Assam   (Rainfall data) (2009-10).