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Diversity and Abundance of Ichthyofaunal Species in Karingali Wetland of Central Kerala, India

Kripa Mariam Mammen1,*, M.G. Sanal Kumar1
1Department of Zoology, N.S.S. College Pandalam, Pathanamthitta- 689 501, Kerala, India.
Background: Karingali wetland is a collection of wetlands in Alappuzha and Pathanmthitta district. It is one of the major wetland paddy fields of central Travancore and had been considered as the rice bank of Mavelikara kingdom. This wetland has not yet been the subject of study. The present study is an inventorization of fish species in this wetland.This will eventually be utilised as a database.

Methods:  The study areas were divided into five sites; fish samples were collected monthly for a period of  June 2020 – May 2022. The collected fish samples were stored in 10% formalin solution and  identified with the help of standard literature.

Result: During the course of the current study, a total of 35 species from 11 orders were discovered from the Karingali wetland. Cypriniformes, Siluriformes, Perciformes, Anabantiformes, Cichliformes, Beloniformes, Elopiformes, Synbranchiformes, Gobiiformes, Clupeiformes and Mugiliformes were the principal orders. The diversity value ranges high during march and low in July. Even though Karingali wetland  are not as much polluted but at the verge of contamination.
Wetlands serves an important role in human survival. They are among the most prolific habitats on Earth; cradles of biological diversity that supply the water and production essential to the survival of innumerable plant and animal species. The Ramsar Convention defines wetlands as areas of marsh, fen, peat land, or water, whether natural or manmade, long-lasting or momentary, with water that is still or flowing, fresh, brackish, or salt, including regions of marine water, whose depth at low tide does not exceed six meters (Ramsar Convention Secretariat, 2013). There are five different types of wetlands: oxbow lakes, freshwater lakes, freshwater ponds, marshes, swamps and bogs and reservoirs (Kar et al., 2007). Of all vertebrates in the world, fish make up nearly half. There are 1,027 different species of freshwater fish in India, including native, alien and secondary species. The wetlands serve as water filters. They convert dissolved nitrogen into nitrogen gas, trap pollutants like heavy metals and phosphorus in their soils and decompose suspended particles to kill hazardous bacteria. For the various advantages, or “ecosystem services,” they offer humanity, including freshwater supply, food and building materials, biodiversity, flood control, groundwater recharge and climate change mitigation, they are important. Although the importance of wetlands for the preservation of fish and wildlife has long been understood, other advantages, such as the preservation of biodiversity, the maintenance of water quality, the regulation of water recharge and discharge, etc., have only recently come to light.

Freshwater fish are one of the most threatened taxonomic groups because of their high sensitivity to the quantitative and qualitative alteration of aquatic habits. Fishes are very important from the biodiversity point of view living in different ecosystems, habitats and niches of aquatic environment. Over 18,000 different species of fish are thought to exist in freshwater biomes, making them one of the world’s most productive and diversified ecosystems (Fricke et al., 2020). Fish make up almost half of all vertebrates in the world and are the most prevalent class of vertebrates in terms of quantity and diversity in size, biology, form and habitat. In addition to serving as a vital source of water for drinking, farming, recreation and sewage disposal, wetlands also significantly support a sizable fishery. It not only complements a healthy diet but also provides the local fishing community with a means of subsistence.
 
Description of the study area
 
‘Karingali puncha’ is a collection of wetlands of Alappuzha and Pathanamthitta districts (Fig 1). It is one of the major wetland paddy fields of central Travancore and had been considered as the rice bank of Mavelikkara kingdom. The area falls under 4 panchayaths (Pandalam Thekkekkara‚ Nooranad‚ Palamel and Thumpamon) and Pandalam municipality. About 28 cultivating wetlands including Mavara‚ Karivellooor‚ Chiramudi‚ Puthuvakkal‚ Shasthampadi‚ Chittilappadam‚ Ampadakam‚ Noorukodi and Nedumpadakam‚  coming under two sections of the total land area: Mavera (near Pandalam) and Karingali (around the Karingali thodu‚ which is flowing through the centre of the wetland collection). The rivulets and streams of padashekharam are emptying to River Achencovil.

Fig 1: Map showing the Karingali Wetland.


 
Sample collection and preservation
 
The study areas were divided into five sites. Nedumpadakam (S1), Chittilappadam (S2), Puthuvakkal (S3), Mavara (S4) and Chiramudi (S5). Nedumpadakam is an area encircled by deep waters. Puthuvakkal is a land covered with various types of vegetation, Chittilappadam and Chiramudi are paddy fields and Mavara is a rocky agricultural area. From June 2020 to May 2022, monthly fish samples were collected with the assistance of local fishermen, samples were collected using a variety of fishing nets, including cast nets, gill nets and traps. Collected samples were preserved in 10% formalin solution. Prior to preservation, photographs were taken. The standard keys from Jhingran and Thalwar (2002); Day (1889); Easa and Shaji (2003) and Jayaram (2012) were used to accomplish the identification. Software from Past 3 and Biodiversity Professional were used to compute the biodiversity indices.
A total of 35 piscine species from 28 genera of 18 families and 11 orders were found in the Karingali wetland over the course of the current study. The prominent orders were Cypriniformes, Siluriformes, Perciformes, Anabantiformes, Cichliformes, Beloniformes, Elopiformes Synbranchiformes, Gobiiformes, Clupeiformes and Mugiliformes (Table 1). Horabagridae, Bagridae, Pangasiidae, Heteropneustidae and Siluridae are the families that belongs to the Order Siluriformes which represent more in number, whereas Channidae, Osphronemidae and Anabantidae are the three families recorded for the Order Anabantiformes. Ambassidae and Nandidae, two families in the Order Perciformes, were reported, with the remaining orders having one family each.

Table 1: List of fish species collected from Karingali wetland during the period of June 2020 to May 2022.



Whereas Elopiformes and Clupeiformes were the least frequently reported, the order Cypriniformes were the most numerous. There are more species in the Cyprinidae family. All five study regions reported identifying Channa striata, Anabas testudineus, Xenentodon cancila, Amblypharyngodon melettinus, Rasbora daniconius, Puntius mahecola, Heteropneustes fossilis and Dawkinsia filamentosa. Nevertheless, Nedumpadakam (site-1) were the only place in which Channa diplogramme, Pangasinodon hypothalamus, Megalops cyorinoides and Stolephorus indicus were identified. Among which, Amblypharyngodon melettinus and the Puntius species, which were found in substantial numbers in this wetland, were much more numerous than Pangasinodon hypothalamus and Channa micropeltes species.

The only family listed for the order Cypriniformes was Cyprinidae, which has 11 species within 8 genera. The species were Amblypharyngodon melettinus, Rasbora daniconius, Tor khudree, Puntius euspilurus, Puntius mahecola, Puntius sophore, Dawkinsia filamentosa, Labeo dussumeri, Systomus chryseus, Systomus rufus, Hypselobarbus curmuca.

During the study period, seven species from genus and five families of the order Siluriformes were reported. Horabagrus brachysoma, Mystus oculatus, Mystus armatus, Pangasinodon hypothalamus, Heteropneustes fossilis, Wallago attu and Ompok malabaricus are among the species on the list. The least frequently observed species from the Karingali wetland is Pangasinodon hypothalamus, which belongs to this order.

Three species from two genus comprise the Order Perciformes. They were Parambassis dayi and Parambassis thomassi from Ambassidae family, Nandus from Nandidae, the order Anabantiformes was represented by 5 species that are members of 3 genera and 3 families. Pseudosphromenus cupanus from the Osphronemidae, Channa diplogramme, Channa micropeltes, Channa striata (Channidae), Anabas testudineus (Anabantidae). The only family identified from the order Cichliformes is Cichlidae. The three species were Etroplus suratensis, Pseudoentroplus maculatus and Orechromus niloticus.

Only one species, Xenentodon cancila of the Belonidae family, comprises the Order Beloniformes. Another solitary species was Megalops cyorinoides of the Megalopidae family of the order Elopiformes. The other orders that had a single species represented them were (Macrognathus fasciatus) Gobiiformes (Glossogobius giuris) Clupeiformes (Stolephorus indicus) and Mugiliformes (Mugil cephalus).

The percentage composition among various orders reveals that  the order Cypriniformes were represented by 42%, Siluriformes 15%, Perciformes 5%, Anabantiformes 12%, Cichliformes 12%, Beloniformes 5%, Elopiformes 1% Synbranchiformes 2%, Gobiiformes 2%,  Mugiliformes  3% and Clupeiformes 1% (Fig 2).

Fig 2: Graph showing order wise population density of fish species.



Fisheries in India have great potential of contributing to the food security of the country. Reservoirs and lakes are the main resources exploited for inland fisheries and understanding of fish faunal diversity is a major aspect for its development and the sustainability management. Fisheries in India have great potential of contributing to the food security of the country. Reservoirs and lakes are the main resources exploited for inland fisheries and understanding of fish faunal diversity is a major aspect for its development and the sustainability management. Fisheries in India have great potential of contributing to the food security of the country. Reservoirs and lakes are the main resources exploited for inland fisheries and understanding of fish faunal diversity is a major aspect for its development and the sustainability management.

In Karingali wetland, cyprinids have been discovered to be dominant. Additionally, Das and Nath (1966); Tilak (1971); Malhotra and Dutta (1975); Dutta and Malhotra (1984); Dutta and Kour (1999); Dutta (2003); Johnson and Arunachalam (2010); Kantaraj et al., (2011); Hoque Rabiul (2023) have reported on the dominance of cyprinids. These three Orders Cypriniformes, Siluriformes are the most prevalent groups in the freshwater bodies hence the findings indicated above are typical (Rahman, 2005). Due to their high adaptive behaviour and capacity to inhabit the various habitats that are available to them, cyprinids predominate in all research sites. Nisa et al., 2021). The same point of view has been supported by several researchers (Gandotra et al., 2015; Wani et al., 2015).

The diversity and abundance of the Karingali Wetland were determined using the Shannon-Weiner, Simpson’s, Margalf, Richness and Eveness indices. The Simpson’s dominance index ranges from 0.04284 to 0.08185 (Table 3). S3 recorded the greatest value and S1 reported the lowest value. The value demonstrates a peak in July and a slow decline in March. Whereas the range of the Shannon-Weiner index value is 2.632 to 3.212 (Table 2). The highest values were from S1 and the lowest values from S3. March marked the Shannon-Weiner index’s peak and July its low point. The lower dominance value suggests that individual species are not quantitatively significant. This trait once again supports the findings of (Sharma and Sharma, 2008). Wilhm and Dorris (1968) assert that clean water is specified if the Shannon’s index (H’) value is greater than three. A score between 1 and 3 indicates generally clean water. Because of anthropogenic activity and the discharge of domestic sewage, the study area were at the verge of pollution. The evenness value ranges from 0.7567 (S4)- 0.9818 (S5) (Table 4). Evenness levels peaked in February and declined in July. The Margalaf richness index was peak in S1 at 5.189 and least in S3 at 3.112. (Table 5). March had seen the greatest values, while February had seen the lowest values. In this study, January and February have seen highest number of freshwater fish recorded. Due to the absence of rainfall, the water depth has been lowered to the barest minimum, allowing fisherman to use their fishing gear more efficiently.

Table 2: Shannon-Weiner index of fish species in Karingali wetland.



Table 3: Simpson’s dominance index of fish species in Karingali wetland.



Table 4: Evenness index of fish species in Karingali wetland.



Table 5: Margalf index of fish species in Karingali wetland.



Rising water levels during the rainy season in tropical environments with seasonal flood pulses cause fish to travel laterally onto floodplains or longitudinally upstream to spawn and feed. Junk et al. (1983) Winemiller and Jepsen (1998). Seasonal rainfall may have had an impact on nutrient inputs, affecting the usage of fish habitat, the availability of food resources and reproductive effort. Archis and Krik (2018) Overfishing, alien species invasion, uncontrolled water pollution from different sources causes and damaging fishing techniques are considered to be the main concerns to fisheries management in the fresh water (Dinesh Kumar et al., 2020). The loss in fish variety is caused by habitat destruction, fishing pressure and foreign fish invasion (Lakra et al., 2008; 2009). In rivers, lakes with river sources and reservoirs, fish populations’ abundance varies greatly from year to year and the relative frequency of various species varies in population. Floods and variations in rainfall have an impact on this change. Spawning, growth and survival rates are improved by the expanding area and flood flow time (Hashemi, 2015).

Freshwater fish variety is decreasing as a result of the combined and interrelated effects of overfishing, contamination of aquatic environment, altered flow patterns, habitat degradation and exotic species invasion (Dudgeon, 2006). The increase in polluting inputs, including as industrial effluents, pesticides and fertilisers from aquaculture, agriculture and home sewage, was caused by an expanding population and more intensive land use (Adikari, 2009). The primary cause of freshwater declining water quality is because of entry of industrial effluents and other pollutants through inflowing drains (Rao and Rao, 2000; Rao and Shekar, 2003). It has been proposed that foreign species introduced for various reasons could constitute a hazard to the local fish population. Recreational activities and other anthropogenic activities are frequent in this wetland. These techniques will affect the wetland and leads to habitat destruction of fish species. Previous researches about freshwater habitat concurs the same (Raju and Simachalam, 2014).

According to Nisa (2021), anthropogenic activities like as fishing pressure, pollution and destroying habitat all have a direct correlation to one another. It is critical to emphasize that sites 1 and 4 have the highest level of anthropogenic activity, such as habitat destruction, runoff from agricultural regions, garbage disposal and exploitation. The least diversity index is justified because fish habitat and water quality are being merely destroyed. The less diverse fish fauna in the wetland may be attributed to habitat degradation, over-exploitation, the random destruction of young fish due to unregulated fishing pressures and other factors. The findings from (Siddiq et al., 2013; Galib et al., 2009 and Chakraborty and Mirza, 2007), which found about the same causes for the loss in fish variety, support the conclusions from the present study.
The Karingali Wetland is found to support a remarkably rich fish diversity and serves as a possible source of income for the local people. A total of 35 species from 28 genus of 18 families and 11 orders were reported from the Karingali wetland during the study period. The major orders were Cypriniformes, Siluriformes, Perciformes, Anabantiformes, Cichliformes, Beloniformes, Elopiformes Synbranchiformes, Gobiiformes, Clupeiformes and Mugiliformes. The percentage composition among various  orders reveals that  the order Cypriniformes were represented by 42%, Siluriformes 15%, Perciformes 5%, Anabantiformes 12%, Cichliformes 12%, Beloniformes 5%, Elopiformes 1% Synbranchiformes 2%, Gobiiformes 2%, Mugiliformes 3% and Clupeiformes 1%. The Cyprinidae family represent more number of individual species. The simpson’s dominance index goes from 0.017 to 0.069 while the Shannon-Weiner index value spans from 0.985 to 1.428. Even though Karingali wetland are not as much polluted but at the verge of contamination. Because of human activity, agricultural pesticides and fertilisers  and in addition, excessive reclamation and contamination from other sources are causing wetlands to lose some of their original qualities. As a result of the loss of biodiversity, there will soon be a shortage of basic foods and water. To effectively safeguard our wetlands and maintain wildlife for future generations, it is crucial to be aware of the situation. The preservation of fish diversity is crucial for preserving the ecological, dietary and economical balance.
All authors declared that there is no conflict of interest.

  1. Adhikari, S., Ghosh, L., Giri, B.S. and Ayyappan, S. (2009). Distributions of metals in the food web of fishponds of Kolleru Lake, India. Ecotoxicology and Environmental Safety. 72(4): 1242-1248.

  2. Archis, R. Grubg and Kirk, O. Winemiller. (2018). Spatiotemporal variation in wetland fish assemblages in the Western Ghats region of India. Knowledge and Management of Aquatic Ecosystems. (419): 35. DOI:10.1051/kmae/2018023.

  3. Chakraborty, B.K. and Mirza, M.J.A. (2007). Study of aquatic biodiversity of Gharia beel of Bangladesh, West Bengal, India: West Bengal Weed Science Society. Journal of Crop and Weed. 3(1): 23-34.

  4. Das, S.M. and Nath, S. (1966). The Icthyofauna of Jammu province (J&K). Kashmir in Science. 2: 65-78.

  5. Day, F. (1889). The Fauna of British India: Fishes. Today and Tomorrow Printers and Publishers. New Delhi, 1: 548.

  6. Dinesh, K., Ashish, K.M., Laxmi Prasad., Singh, C.P. Radhakrishnan, K.V. and Somasekara, S.R. (2020). Fish biodiversity and its diversity indices in the Himalayan River Ghaghara at Northern India. Journal of Entomology and Zoology Studies. 8(6): 1559-1564.

  7. Dudgeon, D., Arthington, A.H., Gessner, M.O., Kawabata, Z.I., Knowler, D.J., Lévêque, C. and Sullivan, C.A. (2006). Freshwater biodiversity: Importance, threats, status and conservation challenges. Biological Reviews. 81(2): 163-182.

  8. Dutta, S.P.S. (2003). Fish fauna of Poonch District, Jammu region, Jammu and Kashmir State. Journal of Aquaculture and Biology. 4: 241-246.

  9. Dutta, S.P.S. and Kour, H. (1999). Some new fish records for Jammu (J&K). Oriental Sciences. 4: 45-47. 

  10. Dutta, S.P.S. and Malhotra, Y.R. (1984). An up-to-date checklist and a key to identification of fishes of Jammu. Jammu University. A Review. 2: 65-92. 

  11. Easa, P.S. and Shaji, C.P. (2003). Biodiversity Documentation for Kerala Part 8. Kerala Forest Research Institute. 126.

  12. Fricke, R. Eschmeyer., W.N. and Fong, J.D. (2020). Eschmeyer’s Catalog of Fishes: Species by Family/subfamily [Internet]. San Francisco: California Academy of Science.

  13. Galib, S.M., Samad, M.A., Mohsin, A.B.M., Flowra, F.A. and Alam, M.T. (2009). Present status of fishes in the Chalan Beel- the largest beel (wetland) of Bangladesh. International Journal Animal Fisheries Science. 2(3): 214-218.

  14. Gandotra, R. and Sharma, P. (2015). Study of Ichthyofaunal diversity in a stream in Sunderbani district Rajouri, Jammu (J&K).  International Journal of Multidisciplinary Research and  Development. 2: 401-404.

  15. Hashemi, S.A., Ghorbani, R., Kymaram, F., Hossini, S.A., Eskandari, G. and Hedayati, A. (2015). Fish species composition, distribution and abundance in Shadegan Wetland. Fisheries  and Aquaculture Journal. 6:2. DOI: 10.4172/2150-3508. 1000128.

  16. Hoque Rabiul, Das, S., Biswas, P., Dey, A. (2023). Icthyofaunal diversity of the river padma at Murshidabad, West Bengal. Agricultural Science Digest. 43(4): 568-571. doi: 10.18805/ag.D-5714.

  17. Jayaram, K.C. (2012). The Freshwater Fishes of Indian Region, Narendra Publishing House, Delhi, India.

  18. Jhingran, A.G. and Talwar, P.K. (2002). Inland Fishes of India and Adjacent Countries. New Delhi, Oxford and IBH Publishing Co.

  19. Johnson, J.A. and Arunachalam, M. (2010). Relations of physical habitat to fish assemblages in streams of Western Ghats, India. Applied Ecology and Environmental Research. 8(1): 1-10.

  20. Junk, W.J., Soares, G.M. and Carvalho, F.M. (1983). Distribution of fish species in a lake of the Amazon river floodplain near Manaus (Lago Camaleão), with special reference to extreme oxygen conditions. Amazoniana: Limnologia et Oecologia Regionalis Systematis Fluminis Amazonas. 7(4): 397-431.

  21. Kantaraj, G.S., Thirumala, S., Kiran, B.R. (2011). Fish diversity in relation to physico-chemical characteristics of Bhadra reservoir of Karnataka, India. Advances in Applied Science  Research. 2(5): 34-47.

  22. Kar, D., Barbhuiya, H. and Saha, B.  (2007). Wetland Diversity in Assam: Their Present Status. Proceeding of Taal: The 12th World Lake Conference. 1844-1857.

  23. Lakra, W.S., Singh, A.K., Ayyappan, S. (2008). Fish Introductions in India: Status, Potential and Challenges. Narendra Publishers, New Delhi, India.

  24. Lakra, W.S., Singh, A.K., Mahanta, P.C (eds) (2009). Fish Genetic Resources. Narendra Publishers, New Delhi.

  25. Malhotra, Y.R. and Dutta, S.P.S. (1975). On Two New Fish Species from Jammu Along with the Checklist of Fishes Inhabiting Jammu Division of J&K State, India. Proceedings of the National Academy of Sciences, India. 42: 153-162.

  26. Nisa, R.U., Gupta, K., Wani, S. M., Allie, K.A. and Kouser, N. (2021). A study on diversity and ecology of ichthyofauna of Rajouri district, Jammu and Kashmir, India. Records of the Zoological Survey of India. 120(4): 363-372.

  27. Rahman, A.K.A. (2005). Freshwater Fishes of Bangladesh, second edition. Zoological Society of Bangladesh, Department of Zoology, University of Dhaka, Dhaka. 1000. 263. 

  28. Raju, C.S., Sekhara, J.C. and Simhachalam, G. (2014). Biodiversity and conservation status of Ichthyofauna of Lake Kolleru Andhra Pradesh, India. International Journal of Scientific Research Zoology. 3(5): 555-563.

  29. Ramsar Convention Secretariat. (2013). The Ramsar Conventioin  Manual, A Guide to the Convention on Wetlands (Ramsar, Iran, 1971), 6th Edition. Ramsar Convention Secretariat, Gland, Switzerland, 103 pp.

  30. Rao, A.S. and Rao, P.R. (2000). Environmental impact of aquaculture on Kolleru Lake. Indian Journal of Environment and Toxicology. 10(1): 1-4.

  31. Rao, P.M. and Sekhar, P. (2003). A Profile of Ecological Disturbances of Kolleru Lake of Andhra Prasdesh, In: Environment, Pollution and Management, [Kumar, A., Bohra, C. and Singh, L.K.]. New Delhi.

  32. Sharma, Venot, J., B.R. and Rao, K.V. (2008). The Lower Krishna Basin Trajectory: Relationships between Basin Development and Downstream Environmental Degradation. 125. IWMI.

  33. Siddiq, M.A., Miah, M.I., Ahmed, Z.F. and Asadujjaman, M. (2013). Present status of fish, fishers and fisheries of Dogger Beel in Hajigonj Upazila, Chandpur, Bangladesh. Journal of Aquatic Science. 1(2): 39-45.

  34. Tilak, R. (1971). The fishes of river Tawi and its tributaries (Jammu) with notes on ecology. Records of Zoological Survey of India. 56: 189-232.

  35. Wani, O.A. and Gupta, U.S. (2015). A study on Ichthyofaunal diversity of Sagar lake, Madhya Pradesh, India. International Journal of Biodiversity and Conservation. 7(3): 126-129.

  36. Wilhm, J.L. and Dorris, T.C. (1968). Biological parameters for water quality criteria. Bioscience. 18: 477-481.

  37. Winemiller, K.O. and Jepsen, D.B. (1998). Effects of seasonality and fish movement on tropical river food webs. Journal of Fish Biology. 53: 267-296.

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