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SESSION-3: Aquatic Biodiversity
PAPER-5: Nutrient status of lentic water bodies and
diversity of Aquatic Macrophytes- Narayana J
CONTENTS-
Abstract
Introduction
Study Area and Methodology
Results and Discussions
References
Abstract | up | previous | next | last |
Lentic water bodies receive nutrients from allochthonous and autochthonous sources and they promote the succession of aquatic macrophytes. The present study comprises nutrient condition of sediment and water, and its influence on the growth and diversity of aquatic plants. During the study period (1999-2000), water and sediment samples were collected and analysed for calcium (Ca 2+ ), magnesium (Mg + ), sodium (Na + ), potassium (K + ), nitrates (NO 3 + ) and phosphates (PO 4 3- ). Similarly aquatic macrophytes were collected and identified to know the distribution and diversity of macrophytes. The present study concluded that, increase in the nitrate and phosphate concentration both in sediment and water, influence the distribution and diversity of macrophytic vegetation and luxuriant growth with great succession of dominant species was encountered.
Introduction | up | previous | next | last |
Aquatic plants play a key role in biogeochemical cycles and food webs of living things in the lentic water bodies. On the other hand aquatic plants are primary producers of food in aquatic ecosystem, and further the absence of aquatic flora may also lead to the absence of fauna. Distribution of macrophytic plants and abundance also indicate the water quality. In natural ecosystem, macrophytes remove both toxic and non-toxic elements in the sediments and water (Narayana and Somashekar, 1997). The trophic status is mainly influenced by the variety of communities and indicator species occurring at the source. Moreover, metabolic activities of macrophytic communities accelerate the physico-chemical conditions of the stream. Submerged aquatic macrophytes are one of the most important components of the littoral zones of lakes. Field studies conducted by Carpenter and Lodge (1986), Balls et al ., (1989) and Sondergaard et al ., (1996) evidenced that submerged macrophytes have an important role in restoration of shallow eutrophic lakes. Therefore, from an engineering point of view, evaluation of life cycles of macrophytes is a key issue before using them in restoration of lakes (Carpenter and Adams, 1977; Asaeda and Bon, 1997).
Macrophytes also take up a large amount of nutrients from the sediment and water. But after death and decay, the nutrient load is again increased in the sediment. In the succeeding decomposition process, accumulated organic matter and nutrients are released, which has a significant influence on the lake ecosystem. The release of ammonia and phosphorous raises the nutrient concentration in the overlying waters and the oxygen consumption in the chemical and biological decomposition process may decrease the dissolved oxygen level in the overlying waters as well as sediments (Jewell, 1971; Pereira et al ., 1994).
Study Area and Methodology | up | previous | next | last |
Sediment and water samples were collected from four sites namely Lakkavally, Rangenahally, Duglapura and Kadlekere ponds. The study area is located in malnad region (Western Ghat region) situated 15 kilometers away from Bhadra wild life sanctuary and Bhadra reservoir. The study area lies at latitude of 13º 42' 10" N and longitude 75º 38º 20" S. The source of water to the ponds is from Bhadra canal linked from Bhadra river. Further the third sampling station namely Duglapura pond is considered as a reservoir, and serves drinking water needs of people of Tarikere. The different physico-chemical parameters such as Ca 2+ , Mg + , Na + , K+, PO 4 -3 and nitrogen content ware analysed using the standard methods (APHA, 1992). Similarly, aquatic plants were also collected and preserved for identification. The standard books and manuals were used for identification. (Fasset, 1975; Cook, 1974; Haslam, 1971; and Britto, 1991).
The present data reveals that the concentration of all inorganic ions in the sediment and water are variable from different ponds. The average values of Ca 2+ , Mg 2+ , Na + , K + , PO 4 -3 and NO 3 + are presented in Table 1.
Table 1. Average values of Nutrient concentration in water and sediment samples
Parameters |
P 1 |
P 2 |
P 3 |
P 4 |
||||
W |
S |
W |
S |
W |
S |
W |
S |
|
Calcium (Ca 2+ ) |
51.21 |
31.02 |
14.29 |
41.25 |
36.40 |
27.84 |
52.09 |
34.78 |
Magnesium (Mg + ) |
18.48 |
40.08 |
16.79 |
48.62 |
36.11 |
30.85 |
48.98 |
42.12 |
Sodium (Na + ) |
0.82 |
4.18 |
0.34 |
2.64 |
5.26 |
35.31 |
6.16 |
44.13 |
Potassium (K + ) |
1.05 |
13.27 |
0.72 |
5.39 |
0.08 |
14.71 |
0.23 |
18.48 |
Phosphorous (PO 4 3-) |
0.31 |
14.6 |
0.26 |
6.31 |
0.64 |
7.58 |
0.90 |
9.013 |
Nitrogen (NO 3 + ) |
0.26 |
6.24 |
0.17 |
4.29 |
0.63 |
0.68 |
0.77 |
0.93 |
Index
P 2 = Rangenahalli pond S = Sediment samples
P 3 = Duglapura pond (Values in mg/kg in sediment)
P 4 = Kadlekere pond (Values in mg/l in water).
The results indicate that the calcium ions show higher concentration in water samples from Lakkvally pond compared to other sampling stations. Similarly Mg + values show higher concentration in sediment at Lakkavally and Rangenahally. Similarly the other parameters such as Na + and K + , phosphorous and nitrogen show higher concentrations in sediment than water.
Distribution of aquatic plants in each pond was determined to understand the species diversity, abundance and occurrence of rare species. The presence and absence of species was noted and is presented in Table 2. In the present study twenty-eight different species of aquatic plants are identified from all the ponds. But species distribution from each pond is greatly varied, which may be due the physico-chemical characteristics of water and sediment. The disturbance from human and domestic activity leads to the loss of macrophytic vegetation.
Table 2. Distribution and species diversity of aquatic plants recorded from different ponds
Plant species |
P 1 |
P 2 |
P 3 |
P 4 |
|
01. |
Azolla pinnata |
- |
+ |
+ |
+ |
02. |
Bacopa monnieri L. |
- |
- |
+ |
- |
03. |
Ceratophyllum demersum L. |
+ |
+ |
+ |
- |
04. |
Convolulus arvensis |
- |
- |
+ |
+ |
05. |
Colocasia esculantus (L) fabr. |
- |
- |
- |
+ |
06. |
Cyperus rotundus L. |
+ |
+ |
+ |
+ |
07. |
Cyperus diffuses Vahl. |
- |
- |
+ |
+ |
08. |
Hydrilla verticellata (L. F) Royle |
- |
+ |
- |
+ |
09. |
Ipomea aquatica L. Forsk. |
+ |
+ |
+ |
+ |
10. |
Jussiea repens L. |
+ |
+ |
+ |
+ |
11. |
Jussiea suffruticosa L. |
+ |
+ |
- |
- |
12. |
Leersia hexandra Sw. |
- |
- |
- |
+ |
13. |
Marsilea minuta |
- |
- |
+ |
+ |
14. |
Marsilea quadrifolia |
- |
+ |
- |
- |
15. |
Monochoria vagenalis Burm. |
+ |
+ |
+ |
- |
16. |
Najas minor All. |
+ |
- |
+ |
+ |
17. |
Nelumbium nucifera Gaertn. |
- |
+ |
- |
- |
18. |
Nymphaea nelambo L. |
- |
- |
+ |
+ |
19. |
Nymphaea stellata Willd. |
- |
+ |
- |
- |
20. |
Pteris sp. |
+ |
+ |
+ |
+ |
21. |
Pistia stratiotes L. |
+ |
- |
- |
- |
22. |
Polygonum glabrum Willd. |
+ |
+ |
+ |
+ |
23. |
Polygonum hydropiper L. |
- |
- |
+ |
+ |
24. |
Sagittaria obtusifolia L. |
- |
- |
- |
+ |
25. |
Setaria sp. Beauv. |
- |
- |
+ |
+ |
26. |
Trapa bispinosa Roxb. |
+ |
+ |
- |
- |
27. |
Typha angustata L. |
+ |
+ |
+ |
+ |
28. |
Zizania aquatica (Wildrice) |
- |
- |
+ |
+ |
Index : + = Present, - = Absent.
It is confirmed that Lakkavally pond is rich in few aquatic plants such as Ceratophyllum demersum, Jussiea repens, Monochoria vaginalis, Najas minor, pteris, Pista stratiotes and Polygonum sp . The pond receives water from surrounding paddy fields and sewage from Lakkavally town. Due to this, the pond has become highly eutrophic. . On the other hand, sediment load has increased due to the runoff from paddy fields. Thus lake depth is slowly reduced, and it supports rich semi-aquatic plants such as Cyperus and other grass species.
Distribution and species diversity of macrophytic vegetation at Rangenahally pond supports rich aquatic and semi-aquatic plants. The pond is surrounded by paddy fields, the run-off has led to the increase in nutrient load. In addition to this, farmers have encroached the catchment area of the lake and now half of the lake is totally filled with sediment and covered with semi-aquatic plants like Polygonum members, Cyperus rotundus, Grass family, Ipomea aquatica and other plants. Similarly, floating and submerged plants namely Azolla pinnata, Ceratophyllum demersum, Hydrilla verticillata, Jussia sp., Monochoria vaginalis, Nelumbo nucifera, Nymphaea sp. , Trapa bispinosa and pteridophytic plants such as pteris are abundant.
The third sampling station called as Duglapura pond is considered as a clean water pond, because Bhadra canal water is linked to the pond for pumping drinking water to Tarikere city. Interestingly this pond also supports a number of different species of aquatic and semi-aquatic plants. Interestingly Typha latifolia covers the pond and some of the semi-aquatic plants support rich bird diversity. Finally Kadlekere pond, has a half moon shaped structure and is also surrounded by paddy fields. Comparatively sediment load is less in Kadlekere and Duglapura ponds.
A number of investigators studied the lentic ecosystem and concluded that the physico-chemical characters influence the growth, species distribution, indicator groups and pollution tolerant species (Narayana and Somashekar, 2002). The increasing concentration of phosphorous and nitrogen have important effects on the primary production. Waglenska et al ., 1987 observed a close relationship between phytoplankton abundance and diversity of submerged macrophytes. The dense stands of macrophytes release large amounts of inorganic nutrients (Dawidowicz et al ., 1987).
References | up | previous | next | last |
APHA, (1992). Standard method for the Examination of water and waste water 18 th Ed. New York.
Aseada, T, and Bon, T.V. (1997). Modeling the effects of macrophytes on algal blooming in eutrophic shallow lakes. Ecol. Modeling 104, 261-287.
Balls, H.B., and Moss, B., Irvine, (1989). The loss of submerged plants with eutrophication 1. Experimental design, water chemistry, aquatic plant and phytoplankton biomass in experiments carried out in ponds in the Norfolk Broadland, Freshwater Biol. 22, 71-87.
Britto., S.J. (1991). Macrophytes collection Procedure. St.Joseph collage, Tiruchirapally, pp. 1-33.
Carpenter, S.R. and Adams, M.S. (1977). The macrophyte tissue nutrient pool of a hardwater eutropic lake: implication for macrophyte harvesting, Aquat. Bot., 3, 239-255.
Carpenter, S.R. and Lodge, D.M. (1986). Effects of submerged macrophytes on ecosystem process, Aqua, Bot. 26, 341-370.
Cook, C.D.K.(1974). Water plants of the world. A manual for the identification of the genera of fresh water macrophytes. W.Junk. B.V. Publishers, The Hague, pp 561.
Dawidowicz, P and Gliwicz, Z.M, (1987). Biomanipulation-III, 33: 259-278.
Fasset, (1975), A manual of aquatic vascular plants. The University of Wisconsin press, Madison. pp.405.
Haslam, S.M. (1978). River plants. The macrophytic vegetation and their identification and management, Cambridge University Press, Cambridge.
Jewell, W.J. (1971). Aquatic weed decay: dissolved oxygen utilization and nitrogen and phosphorous regeneration. J. Water Pollut. Control Fed. 43, 1457-1467.
Narayana, J. and R.K. Somashekar, (1997). Heavy metal composition in the sediment and plants of the river Cauvery. Journal of Environment and Pollution, 4(4), 325-328.
Narayana, J and R.K. Somashekar, (2002). Macrophytes diversity in relation to water quality – Investigation on river Cauvery. In: Ecology and conservation of lakes, reservoirs and rivers. ABD Publishers, Jaipur.
Pereira, A., Tassin, B., and Jorgensen, S.E, (1994). A model for decomposition is the down vegetation in an Amazonian reservoir Ecol. Modeling – 75176, 447-458.
Sondergaard, M. Brunn, L., Lauridsen, T., Jeppesen, E., and Madsen, T.V., (1996). The impact of grazing waterfowl on submerged macrophytes in Situ experiments in a shallow eutrophic lake. Aquat. Bot. 53, 73-84.
Waglenska, T, Dylinska, L.B., Kartin, T.E. and Spoiska, I, (1987). Ecological pollution, 173-208.
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