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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 3 Issue 5, August 2019 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 978
Species Diversity of Polychaete Worms from Some Selected
Freshwater Environment of Thenkasi District, Tamil Nadu
S. Balasubramanian1, T. Citarasu1, S. Lazarus2, A. Renu2
1Centre for Marine Science and Technology, Manonmaniam Sundaranar University,
Rajakkamangalam, Tamil Nadu, India
2Institute for Environmental Research and Social Education, Nesamony Nagar, Nagercoil, Tamil Nadu, India
How to cite this paper: S.
Balasubramanian | T. Citarasu | S. Lazarus
| A. Renu "Species Diversity of Polychaete
Worms from Some Selected Freshwater
Environment of Thenkasi District, Tamil
Nadu" Published in
International
Journal of Trend in
Scientific Research
and Development
(ijtsrd), ISSN: 2456-
6470, Volume-3 |
Issue-5, August
2019, pp.978-980,
https://doi.org/10.31142/ijtsrd26516
Copyright © 2019 by author(s) and
International Journalof Trendin Scientific
Research and Development Journal. This
is an Open Access
article distributed
under the terms of
the CreativeCommons AttributionLicense
(CC BY 4.0)
(http://creativecommons.org/licenses/by
/4.0)
ABSTRACT
The number of freshwater species in the world is quite small when compared
with the vast number of marine species. Thereareseveral marineformswhich
are penetrated brackish and freshwater but remain unable to breed there
while others have adapted sufficiently to remain for their entire life span.
Polychaetes are commonly found in Indian estuaries, among 152 species
recorded, 119 species from the east coast, 10 species from both east and west
coasts. A total of 8 species were identified along Thenkasi District. Macro
benthic polychaetes highlighted the presence of indicator species at all
stations. Most of the benthic studies explored that Nereididae is the dominant
species. The polychaetes observed throughout this study were a similar size
and this is a clear indication of extreme disturbance imposed on thesediment.
The present findings showmacrobenthicpolychaetediversityrichall alongthe
Thenkasi District of Tamil Nadu.
KEYWORDS: Polychaetes, Nereididae, Estuaries, Diversity, Thenkasi
1. INTRODUCTION
The number of freshwater species in the world is quite small when compared
with the vast number of marine species. There are several marine forms which
are penetrated brackish and freshwater but remain unabletobreed therewhile
others have adapted sufficiently to remain for theirentirelifespan.Polychaetes
are commonly found in Indian estuaries, among 152 species recorded, 119
species from the east coast, 10 species from both east and west coasts.
Many investigations were carried out on the abundance and
distribution of polychaetes in the estuarine environmentsof
the southwest coast of India (Ramachandran et al. 1984,
Sarala Devi et al. 1991a, Prabhu et al. 1993, Sheeba, 2000,
Feebarani, 2009). Among the 34 estuaries of the southwest
coast of India, the largest number of polychaetes species, 19
were recorded in the Cochin Estuary (Ajmal Khan and
Murugesan, 2005). Of some 60 polychaete families, only 7
have been reported as having freshwater representatives.
These are the Nereididae, Nephthyidae, Lumbrineridae,
Spionidae, Capitellidae, Ampharetidae, Sabellidae and
Serpulidae (Wesenberg-Lund, 1958). A large number of
freshwater species are of the families Nereididae and
Sabellidae, The others having fewer than five
representatives. The Nereididae (Blainville, 1818) is among
the most diverse of polychaetefamilies, comprisingover 540
species and 43 genera (Beesley et al. 2000). They are most
common in shallow marine habitats, but the Nereididae are
the ones that have been more economically found in
freshwater environments compared to other polychaete
families (Bakken and Wilson, 2005).
2. Materials and methods
Freshwater species are collected in much the same manner
as marine forms. Those from shore areas and shallow water
are collected with a shovel and a fine sieve. The sediment is
placed in the sieve. Washed through and the remaining
animals then removed. Those from deeper water may be
collected by dredging or by the use of grab samplers the
sediment from which is then washed through a fine sieve.
Polychaetes should be initially preserved in 10% formalin
and subsequently transferred to 70%ethylalcohol. As usual,
whenever possible observations should be made on the
living animal noting such things as coloration, presence of
eyes etc as these may possibly change or disappear in the
preservatives. Collected samples were brought to the
laboratory and sorted out. For the present study samples
were taken from different areas of Thenkasi District, Tamil
Nadu (Table1). The samples were identified by using
standard keys (Southern, 1921, Fauel, 1953, Days, 1967,
Kausal and Binford, 1999, Avnimelech et al. 2001, Bakken
and Wilson, 2005, Gravely, 2005).
IJTSRD26516
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 979
Table1. The geographical position of the study stations
Sl. No Name of the station Latitude Longitude
1 Thrumalaikovil pond 12.86 79.08
2 Kasiviswanathar temple pond 12.73 79.36
3 Chittar River 12.08 79.73
4 Thamirabarani River 12.45 79.85
5 Manimuthar River 12.72 78.99
6 Chervalar Dam 12.29 78.92
7 Adavinainar Dam 12.58 78.95
8 Kadana nathi 12.88 79.10
Table.2. Checklist of species diversity in some selected stations of Thenkasi district
Sl. No Species Family S-1 S-2 S-3 S-4 S-5 S-6 S-7 S-8
1 Laeonereis culveri Nereididae + + +
2 Lycastoides alticola Nereididae + + + + + + + +
3 Lycastopsis humelincki Nereididae + + + + +
4 Namanereis hawaiiensis Nereididae + + + + +
5 Nereies limnicola Nereididae + + + +
6 Nereis auccinea Nereididae + + + + + +
7 Manyunkia speciosa Sabellidae + + + +
8 Mercierella enigmatica Serpulidae + + + +
S-1 Thirumalai Kovil Pond; S-2 Kasiviswanathar temple Pond; S-3 Chittar River; S-4 Thamirabarani River; S-5 Manimuthar
River; S-6 Chervalar Dam; S-7 Adavinainar Dam; S-8 Kadana Nathi
3. Result and Discussion
The species diversity of macro polychaete appendix is given
in Table. 2. A total of 8 species were identified along
Thenkasi District. Macro benthicpolychaeteshighlighted the
presence of indicator species at all stations. Most of the
benthic studies explored that Nereididae is the dominant
species. The polychaetes observed throughout this study
were a similar size and this is a clear indication of extreme
disturbance imposed on the sediment. The present findings
show macrobenthic polychaete diversity rich all along the
district. When compared with other species Lycastoides
alticola was present in all stations and it is the dominant
species when compared with others. Laeonereis culveri
poorly distributed in all stations. In station No. 2, 3, 5, 7 & 8,
the species Laeonereis culveri were absent. Nereis auccinea
present in all stations except station 4 and 7. The
polychaetes observed throughout this study were a similar
size and this is a clear indication of extreme disturbance
imposed on the sediment. The present findings show
macrobenthic polychaete diversity rich all along thedistrict.
4. Reference
[1] Ajmal Khan S., and Murugesan P., 2005, Polychaetes
diversity in Indian estuaries, Indian Journal of Geo-
Marine Sciences, 34:114-119
[2] Avnimelech Y., Ritvo G., Meijer L. E., and Kochba M.,
2001, Water content, organic carbon and dry bulk
density in flooded sediments, Aquacultural
Engineering, 25:25-33.
[3] Bakken and Wilson, 2005. Phylogeny of nereidids
(Polychaeta, Nereididae) with paragnaths Zoologica
Scripta, 34(5): 507-54
[4] Beesley, P. L, Ross G. A. B., Glasby C. J. 2000, Beesley, P.
L., Ross, G. J. B. and Glasby, C. J. 2000. Polychaetes &
Allies: The Southern Synthesis. CSIRO Publishing:
Melbourne. xii + 465pp. A recent overview of
Polychaetes, and related groups including myotomes
(Myzostomida), pogonophorans (Pogonophora),
echiurans (Echiura) and sipunculans (Sipuncula).
[5] Blainvile, 1818. Blainville, H. de. 1818. Mémoire sur la
classe des Sétipodes, partie des Vers àsangrougedeM.
Cuvier, et des Annélides de M. de Lamarck. Bulletin des
Sciences, par la Société Philomatique de Paris.82.
[6] Day, J. H. 1967. A monograph of the Polychaeta of
southern Africa. Part 1. Errantia. Part 2. Sedentaria.
British Museum (Natural History), London. 656(2):87-
88.
[7] Fauvel P., 1953, The Fauna of Indian including Pakistan,
Ceylon, Burma and Malaya: Annelid Polychaeta, the
Indian Press Ltd.
[8] Feebarani J., 2009, Meiobenthos of Cochin backwaters
in relation to macrobenthos and environmental
parameters. Department of Marine Biology,
Microbiology and Biochemistry, School of Marine
Sciences. Kochi, Cochin University of Science and
Technology.
[9] Gravely F. H., 2005, Chaetopoda. IN MUSEUMS, D. O.
(Ed.) Bulletin of the Madras government museum: The
littoral fauna of Krusadai island in the Gulf of Manaar
with appendices on the vertebrates and plant. Madras,
Government of Tamilnadu.
[10] Kaushal S., and Binford M., 1999,Relationshipbetween
C: N ratios of lake sediments, organic matter sources,
and historical deforestation in Lake Pleasant,
Massachusetts, USA,JournalofPaleolimnology,22:439-
442.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 980
[11] Prabhu V. H., Narayan A. C., and Katti R. J., 1993,
Macrobenthic fauna in near-shore sediments off
Gangolli-west coast of India, Indian Journal of Geo-
Marine Sciences, 22:168
[12] Ramachandra U. T., GuptaR. C., and Katti R. J., 1984,
Macrobenthos and sediment characteristics of Mulki
estuary, west coast of India, Indian Journal of Geo-
Marine Sciences, 13:109-112.
[13] Sarala Devi K., Sankarnarayanan V.N., and Venugopal
P., 1991a, Distribution of nutrients in the Periyar River
estuary, Indian Journal of Geo-Marine Sciences, 20:49-
54.
[14] Sheeba P., 2000, Distribution of benthic infauna in the
Cochin backwaters in relation to environmental
parameters. Ph.D. Thesis NIO-RC.Kochi, Cochin
University of Science and Technology.
[15] Southern R. 1921, Polychaeta of the Chilka Lake and
also of fresh and brackish waters in other parts of
India. Memoirs of the Indian Museum.
[16] Wesenberg-Lund, Elise. 1958. Lesser Antillean
polychaetes chiefly from brackish waters, with a
survey and a bibliography of fresh and brackish water
polychaetes. Studies on the Fauna of Curaçao and other
Caribbean Islands. 8:1-41.

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Species Diversity of Polychaete Worms from Some Selected Freshwater Environment of Thenkasi District, Tamil Nadu

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 3 Issue 5, August 2019 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 978 Species Diversity of Polychaete Worms from Some Selected Freshwater Environment of Thenkasi District, Tamil Nadu S. Balasubramanian1, T. Citarasu1, S. Lazarus2, A. Renu2 1Centre for Marine Science and Technology, Manonmaniam Sundaranar University, Rajakkamangalam, Tamil Nadu, India 2Institute for Environmental Research and Social Education, Nesamony Nagar, Nagercoil, Tamil Nadu, India How to cite this paper: S. Balasubramanian | T. Citarasu | S. Lazarus | A. Renu "Species Diversity of Polychaete Worms from Some Selected Freshwater Environment of Thenkasi District, Tamil Nadu" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456- 6470, Volume-3 | Issue-5, August 2019, pp.978-980, https://doi.org/10.31142/ijtsrd26516 Copyright © 2019 by author(s) and International Journalof Trendin Scientific Research and Development Journal. This is an Open Access article distributed under the terms of the CreativeCommons AttributionLicense (CC BY 4.0) (http://creativecommons.org/licenses/by /4.0) ABSTRACT The number of freshwater species in the world is quite small when compared with the vast number of marine species. Thereareseveral marineformswhich are penetrated brackish and freshwater but remain unable to breed there while others have adapted sufficiently to remain for their entire life span. Polychaetes are commonly found in Indian estuaries, among 152 species recorded, 119 species from the east coast, 10 species from both east and west coasts. A total of 8 species were identified along Thenkasi District. Macro benthic polychaetes highlighted the presence of indicator species at all stations. Most of the benthic studies explored that Nereididae is the dominant species. The polychaetes observed throughout this study were a similar size and this is a clear indication of extreme disturbance imposed on thesediment. The present findings showmacrobenthicpolychaetediversityrichall alongthe Thenkasi District of Tamil Nadu. KEYWORDS: Polychaetes, Nereididae, Estuaries, Diversity, Thenkasi 1. INTRODUCTION The number of freshwater species in the world is quite small when compared with the vast number of marine species. There are several marine forms which are penetrated brackish and freshwater but remain unabletobreed therewhile others have adapted sufficiently to remain for theirentirelifespan.Polychaetes are commonly found in Indian estuaries, among 152 species recorded, 119 species from the east coast, 10 species from both east and west coasts. Many investigations were carried out on the abundance and distribution of polychaetes in the estuarine environmentsof the southwest coast of India (Ramachandran et al. 1984, Sarala Devi et al. 1991a, Prabhu et al. 1993, Sheeba, 2000, Feebarani, 2009). Among the 34 estuaries of the southwest coast of India, the largest number of polychaetes species, 19 were recorded in the Cochin Estuary (Ajmal Khan and Murugesan, 2005). Of some 60 polychaete families, only 7 have been reported as having freshwater representatives. These are the Nereididae, Nephthyidae, Lumbrineridae, Spionidae, Capitellidae, Ampharetidae, Sabellidae and Serpulidae (Wesenberg-Lund, 1958). A large number of freshwater species are of the families Nereididae and Sabellidae, The others having fewer than five representatives. The Nereididae (Blainville, 1818) is among the most diverse of polychaetefamilies, comprisingover 540 species and 43 genera (Beesley et al. 2000). They are most common in shallow marine habitats, but the Nereididae are the ones that have been more economically found in freshwater environments compared to other polychaete families (Bakken and Wilson, 2005). 2. Materials and methods Freshwater species are collected in much the same manner as marine forms. Those from shore areas and shallow water are collected with a shovel and a fine sieve. The sediment is placed in the sieve. Washed through and the remaining animals then removed. Those from deeper water may be collected by dredging or by the use of grab samplers the sediment from which is then washed through a fine sieve. Polychaetes should be initially preserved in 10% formalin and subsequently transferred to 70%ethylalcohol. As usual, whenever possible observations should be made on the living animal noting such things as coloration, presence of eyes etc as these may possibly change or disappear in the preservatives. Collected samples were brought to the laboratory and sorted out. For the present study samples were taken from different areas of Thenkasi District, Tamil Nadu (Table1). The samples were identified by using standard keys (Southern, 1921, Fauel, 1953, Days, 1967, Kausal and Binford, 1999, Avnimelech et al. 2001, Bakken and Wilson, 2005, Gravely, 2005). IJTSRD26516
  • 2. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 979 Table1. The geographical position of the study stations Sl. No Name of the station Latitude Longitude 1 Thrumalaikovil pond 12.86 79.08 2 Kasiviswanathar temple pond 12.73 79.36 3 Chittar River 12.08 79.73 4 Thamirabarani River 12.45 79.85 5 Manimuthar River 12.72 78.99 6 Chervalar Dam 12.29 78.92 7 Adavinainar Dam 12.58 78.95 8 Kadana nathi 12.88 79.10 Table.2. Checklist of species diversity in some selected stations of Thenkasi district Sl. No Species Family S-1 S-2 S-3 S-4 S-5 S-6 S-7 S-8 1 Laeonereis culveri Nereididae + + + 2 Lycastoides alticola Nereididae + + + + + + + + 3 Lycastopsis humelincki Nereididae + + + + + 4 Namanereis hawaiiensis Nereididae + + + + + 5 Nereies limnicola Nereididae + + + + 6 Nereis auccinea Nereididae + + + + + + 7 Manyunkia speciosa Sabellidae + + + + 8 Mercierella enigmatica Serpulidae + + + + S-1 Thirumalai Kovil Pond; S-2 Kasiviswanathar temple Pond; S-3 Chittar River; S-4 Thamirabarani River; S-5 Manimuthar River; S-6 Chervalar Dam; S-7 Adavinainar Dam; S-8 Kadana Nathi 3. Result and Discussion The species diversity of macro polychaete appendix is given in Table. 2. A total of 8 species were identified along Thenkasi District. Macro benthicpolychaeteshighlighted the presence of indicator species at all stations. Most of the benthic studies explored that Nereididae is the dominant species. The polychaetes observed throughout this study were a similar size and this is a clear indication of extreme disturbance imposed on the sediment. The present findings show macrobenthic polychaete diversity rich all along the district. When compared with other species Lycastoides alticola was present in all stations and it is the dominant species when compared with others. Laeonereis culveri poorly distributed in all stations. In station No. 2, 3, 5, 7 & 8, the species Laeonereis culveri were absent. Nereis auccinea present in all stations except station 4 and 7. The polychaetes observed throughout this study were a similar size and this is a clear indication of extreme disturbance imposed on the sediment. The present findings show macrobenthic polychaete diversity rich all along thedistrict. 4. Reference [1] Ajmal Khan S., and Murugesan P., 2005, Polychaetes diversity in Indian estuaries, Indian Journal of Geo- Marine Sciences, 34:114-119 [2] Avnimelech Y., Ritvo G., Meijer L. E., and Kochba M., 2001, Water content, organic carbon and dry bulk density in flooded sediments, Aquacultural Engineering, 25:25-33. [3] Bakken and Wilson, 2005. Phylogeny of nereidids (Polychaeta, Nereididae) with paragnaths Zoologica Scripta, 34(5): 507-54 [4] Beesley, P. L, Ross G. A. B., Glasby C. J. 2000, Beesley, P. L., Ross, G. J. B. and Glasby, C. J. 2000. Polychaetes & Allies: The Southern Synthesis. CSIRO Publishing: Melbourne. xii + 465pp. A recent overview of Polychaetes, and related groups including myotomes (Myzostomida), pogonophorans (Pogonophora), echiurans (Echiura) and sipunculans (Sipuncula). [5] Blainvile, 1818. Blainville, H. de. 1818. Mémoire sur la classe des Sétipodes, partie des Vers àsangrougedeM. Cuvier, et des Annélides de M. de Lamarck. Bulletin des Sciences, par la Société Philomatique de Paris.82. [6] Day, J. H. 1967. A monograph of the Polychaeta of southern Africa. Part 1. Errantia. Part 2. Sedentaria. British Museum (Natural History), London. 656(2):87- 88. [7] Fauvel P., 1953, The Fauna of Indian including Pakistan, Ceylon, Burma and Malaya: Annelid Polychaeta, the Indian Press Ltd. [8] Feebarani J., 2009, Meiobenthos of Cochin backwaters in relation to macrobenthos and environmental parameters. Department of Marine Biology, Microbiology and Biochemistry, School of Marine Sciences. Kochi, Cochin University of Science and Technology. [9] Gravely F. H., 2005, Chaetopoda. IN MUSEUMS, D. O. (Ed.) Bulletin of the Madras government museum: The littoral fauna of Krusadai island in the Gulf of Manaar with appendices on the vertebrates and plant. Madras, Government of Tamilnadu. [10] Kaushal S., and Binford M., 1999,Relationshipbetween C: N ratios of lake sediments, organic matter sources, and historical deforestation in Lake Pleasant, Massachusetts, USA,JournalofPaleolimnology,22:439- 442.
  • 3. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD26516 | Volume – 3 | Issue – 5 | July - August 2019 Page 980 [11] Prabhu V. H., Narayan A. C., and Katti R. J., 1993, Macrobenthic fauna in near-shore sediments off Gangolli-west coast of India, Indian Journal of Geo- Marine Sciences, 22:168 [12] Ramachandra U. T., GuptaR. C., and Katti R. J., 1984, Macrobenthos and sediment characteristics of Mulki estuary, west coast of India, Indian Journal of Geo- Marine Sciences, 13:109-112. [13] Sarala Devi K., Sankarnarayanan V.N., and Venugopal P., 1991a, Distribution of nutrients in the Periyar River estuary, Indian Journal of Geo-Marine Sciences, 20:49- 54. [14] Sheeba P., 2000, Distribution of benthic infauna in the Cochin backwaters in relation to environmental parameters. Ph.D. Thesis NIO-RC.Kochi, Cochin University of Science and Technology. [15] Southern R. 1921, Polychaeta of the Chilka Lake and also of fresh and brackish waters in other parts of India. Memoirs of the Indian Museum. [16] Wesenberg-Lund, Elise. 1958. Lesser Antillean polychaetes chiefly from brackish waters, with a survey and a bibliography of fresh and brackish water polychaetes. Studies on the Fauna of Curaçao and other Caribbean Islands. 8:1-41.