2Center for Environmental Nuclear Research, Directorate of Research SRM Institute of Science and Technology, Kattankulathur-603 203
Keywords: Marine gastropods; Invertebrate; Checklist; TAPS; Maharashtra;
The change in spatial scale often supposed to alter the diversity pattern, in the sense that an increased in scale could provide more resources to species and that promote an increased in diversity [9]. In case of invertebrates the second largest group on earth is Mollusc [7]. Intertidal molluscan communities are interlinks for the study of morphological and ecological convergence between geographically and temporally isolated communities [13]. The molluscs are soft bodied animals with long evolutionary history and diversity [6,8]. Based on the habitat the molluscs are classified as terrestrial and aquatic community. Molluscan community structure and their diversity indicate the overall ecosystem health [26]. To investigate the relationship between biodiversity and ecosystem function the intertidal ecosystem is very helpful. The intertidal organisms are under continuous stress by environmental as well as anthropogenic cause, which can be better assessed by studying the responses of these organisms. The advantages behind selection of these organisms are many as they are numerous, accessible, slow moving, easy to collect and suitable for experimental manipulation [14]. Biodiversity essentially reflects ecological quality of the habitat [37]. In current scenario with increased interference of manmade activities in coastal area, the flora and fauna are under threat. Hence, continuous monitoring and record through diversity studies is an important. A baseline checklist of marine gastropods around ecologically importance area of Tarapur is not available till yet. Therefore, the present work was done to achieve the baseline information about the marine gastropods checklist along with physcio-chemical parameters around Tarapur Atomic Power Station (TAPS), Tarapur site area. This study will be assisted any future reference study on marine invertebrates diversity in relation to running of the atomic power plant.
Sampling location |
GPS position |
Importance of location |
TAPS 1 & 2 |
N -19°50.003’ |
Intertidal area near to intake channel (North side) |
Light House |
N -19°50’32.1” |
Intertidal area at the discharge channel of TAPS 1 & 2 (North side) |
Varor |
N -19°54’32.4” |
Reference location, at the distance of 8.00 km from the discharge channel of TAPS 1& 2 (North side) |
TAPS 3 & 4 |
N -19°49.533’ |
Intertidal area near to intake channel (South side) |
Popharan |
N – 19°50.638” |
Intertidal area at the discharge channel of TAPS 3 & 4 (South side) |
Nandgaon |
N -19°45’09.0” |
Reference location, at the distance of 8.00 km from the discharge channel of TAPS 3& 4 (South side) |
The each selected intertidal location was sub-divided into three tidal zone namely High water level (HWL), Mid Water Level (MWL) and Low Water Level (LWL) so that maximum area could get covered. The sampling was started at LWL followed by MWL and then HWL, to get maximum time period for extensive survey. The numbers of sampling techniques are used; the most common for the collection of molluscs is the quadrate sampling [10,11,16,18,23,24]. At each water level four quadrate of 1 m2 were placed at almost equal distance intervals (Approximately 25 m). The gastropods in quadrate were collected by using scraper (Scissor like tool) that skims the animals, since most of the gastropods are not firmly attached to substratum, it become easy to collect them with this tool. The burrowing and organisms present in rock crevices were collected with the help of small spade like material. The gastropods collected from four quadrates at each water level were kept in different plastic container. 5% buffer formaline prepared in sea water were added to containers to avoid putrid smell after death.
The 50g of dried sediment sample were taken for analysis. The sediment texture were analyzed by following Hydrometer method explained in Soil Sampling, Preparation and Analysis, authored by [19] and the result is express in percentage value. The Organic Carbon (Corg %) were estimated by Walkley – Black Wet Combustion Method (1934). All the analysis for water and sediment were repeated thrice for each sample and the average value is taken as the final result.
Seasons |
Water |
pH |
Salinity |
Dissolved |
Ammonia |
Nitrite |
Nitrate |
Phosphate |
MON-2013 |
28-33.75 |
7.7-8.4 |
33.5-35.5 |
6.5-7.8 |
0.7-1.2 |
0.2-0.7 |
0.45-0.7 |
0.5-0.8 |
POST-2013 |
25.3-32 |
7.5-8.0 |
33-35 |
6.1-7.0 |
0.7-1.2 |
0.05-0.8 |
0.4-0.8 |
0.42-1.15 |
PRE-2014 |
28.2-38.5 |
7.1-8.17 |
35-36.3 |
5.9-7.2 |
0.75-1.8 |
0.2-0.5 |
0.18-0.4 |
0.84-1.39 |
Seasons |
Water |
pH |
Salinity |
Dissolved |
Ammonia |
Nitrite |
Nitrate |
Phosphate |
TAPS 1&2 |
27.1-30.5 |
7.9-8.1 |
33-35 |
6.1-7.5 |
0.6-1.22 |
0.2-0.6 |
0.23-0.7 |
0.42-0.84 |
TAPS 3&4 |
27-32 |
7.5-8.4 |
34-35 |
6-6.9 |
0.75-1.1 |
0.2-0.98 |
0.2-0.6 |
0.7-0.88 |
Light House |
27-30.6 |
7.8-8.26 |
33.5-35 |
6.3-7.2 |
0.7-1.8 |
0.3-1 |
0.12-0.8 |
0.54-1.39 |
Popharan |
30.5-38.5 |
7.1-8.15 |
34.5-36.3 |
5.9-7.5 |
0.7-1.2 |
0.3-0.8 |
0.25-0.8 |
0.65-1.15 |
Varor |
26.5-28.2 |
7.7-8 |
33-35.5 |
6.4-7.7 |
0.8-1.25 |
0.1-0.22 |
0.1-0.8 |
0.5-1.16 |
Nandgaon |
25.3-29.5 |
7.9-8.4 |
32.5-35 |
6.1-7.5 |
0.8-1.51 |
0.5-0.94 |
0.2-0.7 |
0.6-1.15 |
Seasons |
Sand (%) |
Silt (%) |
Clay (%) |
Organic carbon (Corg, %) |
MON-2013 |
74.98 - 89.6 |
6.5 -18.4 |
3.6 – 11.5 |
0.65 – 1.91 |
POST-2013 |
73.2 - 90.5 |
5.02 – 10.3 |
3.7 – 17.7 |
0.18 – 1.6 |
PRE-2014 |
73.2 – 92.3 |
6 – 12.3 |
1.7 – 20.7 |
0.04 – 1.32 |
Seasons |
Sand (%) |
Silt (%) |
Clay (%) |
Organic carbon (Corg, %) |
TAPS 1&2 |
82.18 – 92.3 |
5.02 – 9.5 |
1.7 – 9.3 |
0.11 – 1.4 |
TAPS 3&4 |
86.11 – 91 |
5.8 – 8.7 |
2.6 – 6.49 |
0.03 – 1.91 |
Light House |
73.2 – 81.2 |
6.1 – 10.24 |
8.69 – 20.7 |
1.2 – 1.8 |
Popharan |
85.9 – 95.6 |
4.1 – 8.7 |
0.3 – 5.4 |
0.09 – 0.7 |
Varor |
74.98 – 83.7 |
10.3 – 18.4 |
6.62 – 11.08 |
0.9 – 1.68 |
Nandgaon |
84.3 – 89.4 |
6 – 9.5 |
4.2 – 8.9 |
0.65 – 1.1 |
Sl. No. |
Species |
Author |
1 |
Nerita oryzarum |
Récluz, 1841 |
2 |
Nerita undata |
Linnaeus, 1758 |
3 |
Nerita chamaeleon |
Linnaeus, 1758 |
4 |
Nerita polita |
Linnaeus, 1758 |
5 |
Nerita albicilla |
Linnaeus, 1758 |
6 |
Neripteron violaceum |
Gmelin, 1791 |
7 |
Clypeomorus bifasciata |
G. B. Sowerby II, 1855 |
8 |
Pirenella cingulata |
Gmelin, 1791 |
9 |
Cerithium echinatum |
Lamarck, 1822 |
10 |
Cerithium scabridum |
Philippi, 1848 |
11 |
Planaxis sulcatus |
Born, 1778 |
12 |
Supplanaxis niger |
Quoy & Gaimard, 1833 |
13 |
Littoraria undulata |
Gray, 1839 |
14 |
Indothais lacera |
Born, 1778 |
15 |
Semiricinula tissoti |
Petit de la Saussaye, 1852 |
16 |
Semiricinula konkanensis |
Melvill, 1893 |
17 |
Gyrineum natator |
Röding, 1798 |
18 |
Echinolittorina malaccana |
Philippi, 1847 |
19 |
Conus figulinus |
Linnaeus, 1758 |
20 |
Cantharus spiralis |
Gray, 1839 |
21 |
Pollia fumosa |
Dillwyn, 1817 |
22 |
Pollia undosa |
Linnaeus, 1758 |
23 |
Indothais blanfordi |
Melvill, 1893 |
24 |
Engina zea |
Melvill, 1893 |
25 |
Chicoreus brunneus |
Link, 1807 |
26 |
Littoraria scabra |
Linnaeus, 1758 |
27 |
Strigatella scutulata |
Gmelin, 1791 |
28 |
Nassarius stolatus |
Gmelin, 1791 |
29 |
Nassarius jacksonianus |
Quoy & Gaimard, 1833 |
30 |
Turricula tornata |
Dillwyn, 1817 |
31 |
Drupella rugosa |
Born, 1778 |
32 |
Indothais lacera |
Born, 1778 |
33 |
Telescopium telescopium |
Linnaeus, 1758 |
34 |
Conus hyaena |
Hwass in Bruguière, 1792 |
35 |
Turricula javana |
Linnaeus, 1767 |
36 |
Strigatella litterata |
Lamarck, 1811 |
37 |
Echinolittorina vidua |
Gould, 1859 |
38 |
Naria miliaris |
Gmelin, 1791 |
39 |
Lataxiena bombayana |
Melvill, 1893 |
40 |
Tenguella granulata |
Duclos, 1832 |
41 |
Turbo bruneus |
Röding, 1798 |
42 |
Astralium semicostatum |
Kiener, 1850 |
43 |
Clanculus ceylonicus |
G. & H. Nevill, 1869 |
44 |
Astralium stellare |
Gmelin, 1791 |
45 |
Herpetopoma aspersum |
Philippi, 1846 |
46 |
Umbonium vestiarium |
Linnaeus, 1758 |
47 |
Trochus radiatus |
Gmelin, 1791 |
48 |
Cellana radiata |
Born, 1778 |
49 |
Cellana testudinaria |
Linnaeus, 1758 |
50 |
Acmaea achates |
Reeve, 1855 |
51 |
Ocenebra bombayana |
Melvill, 1893 |
- David A. Biodiversity and distribution of marine gastropods (Mollusca) during pre- and post monsoon seasons along the Goa coastline, India. Journal of Marine Biological Association of India. 2013;55:17-24. doi: 10.6024/jmbai.2013.55.1.01720-03
- Appukuttan KK, Ramadoss K. Edible and ornamental gastropod resources. Marine Fisheries Research and Management, Report of Central Marine Fisheries Research Institute, Edited by; VN Pillai and NG Menon, Kerala, India. 2000:525-535.
- Apte D. Molluscan fauna of point Calimere wildlife sanctuary A. Gastropoda. Journal of Bombay Natural History Society. 2004;101(2):201-210.
- Kannapiran E, Kannan L, Purushothaman A, Thangarajdou T. Physico-chemical and microbial characteristics of the coral reef environment of the Gulf of Mannar marine biosphere reserve, India. J Environ Biol. 2008;29(2):215-222.
- Shirke B, Patil A, Rao B, Quadros G, Babu S. Molluscan diversity from the tourist destination of Malvan. Proc UGC Sponsored National Seminar on “Wetlands-Present Status, Ecology & Conservation” ISBN: 978-81-925005-3-9. 2015.
- Bogan AE. Global diversity of freshwater mussels (Mollusca, Bivalvia) in freshwater. Hydrobiologia. 2008;595(1):139-147.
- Bouchet P. The magnitude of marine biodiversity, In: Duarte CM, editor. The Exploration of Marine Biodiversity: Scientific and Technological Challenges. Madrid, Spain: Fundacion BBVA. 2006:32-64.
- Chiba S. Species richness patterns along environmental gradients in island land molluscan fauna. Ecology. 2007;88(7):1738-1746.
- Crawley MJ, Harral JE. Scale dependence in plant biodiversity. Science. 2001;291(5505):864-868.
- Datta SN, Chakraborty SK, Jaiswar AK, venkateshvaran K. Temporal and spatial differences in species diversity in the intertidal region of south Mumbai. Journal of Marine Biological Association, India. 2008;50(1):29-37.
- Datta SN, Chakraborty SK, Jaiswar AK, Ziauddin G. A comparative study on intertidal faunal biodiversity of selected beaches of Mumbai coast. Journal of Environmental Biology. 2010;31(6):981-986.
- FAO. Carpenter KE; Niem VH. (eds) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Volume 2. Cephalopods, crustaceans, holothurians and sharks. Rome. 1998:687-1396.
- Vermeij GJ, Raven H. Southeast Asia as the birth place of unusual traits: the Melongenidae (Gastropoda) of northwest Borneo. Contributions to Zoology. 2009;78(3):113-127.
- Hammond PM. Species inventory, in Groombridge, B. (ed.) Global Biodiversity. Status of the Earth’s living resources, London: Chapman and Hall. 1992:17-39.
- Hornell J. The study of Indian molluscs (part II). J Bombay Nat Hist Soc, 48(3):543-569. Hornell J.1951. Indian molluscs. J Bombay Nat Hist Soc. 1949:1-96.
- Khade SN, Mane UH. Diveristy of bivalve and gastropod molluscs of some localities from Raigad district, Maharashtra, west coast of India. Recent Research in Science and Technology. 2012;4(10):43-48.
- Khade SN. Marine gastropods molluscan diversity from west coast of India. International Journal of Zoology Studies. 2018;3(2):116-119.
- Khade SN, Mane UH. Diveristy of bivalve and gastropod molluscs of some localities from Raigad district, Maharashtra, west coast of India. Recent Research in Science and Technology. 2012;4(10):43-48.
- Tan KH. Soil sampling, preparation, and analysis: Books in soil, plants, and the environment. Taylor & Francis Publisher. 1996:432.
- Kurhe AR, Mane UH, Pawar BA. Studies on marine gastropods mollusks from Ratnagiri coast Maharashtra, India. Journal of Experimental Zoology, India. 2009;12(2):409-414.
- Kurve P, Kurve N, Shenai D, Oak G. Bivalve and Gastropod diversity of Borli Coast, Raigad, Maharashtra. “National conference on Biodiversity: Status and Challenges in Conservation”- “FAVEO-2013”. ISBN: 978-81-923628-1-6.
- Legendre P, Thrush SF, Cummings VJ, Dayton PK, Grant J, Hewitt JE, et al. Spatial structure of bivalves in sand flat: scale and generating processes. Journal of Experimental Marine Biology and Ecology. 1997;216(1-2):99-128.
- Mark ML, Steven NM. Influence of Domestic Wastes on Energetic Pathways in Rocky Intertidal Communities. Journal of Applied Ecology. 1978;15(2):583-595.
- Odum HT, Odum EP. Trophic structure and productivity of a windward coral reef community on Eniwetok Atoll. Ecological Monographs. 1955;25(3):291-320.
- Perry JN, Leibold AM, Rosenberg MS, Dungan J, Miriti M, Jakomulska A, et al. Illustrations and guidelines for selecting statistical methods for quantifying spatial pattern in ecological data. Ecography. 2002;25(5):578-600.
- Romano JA, McClellan-Green P, Rittschof D. Copper pyrithione and diuron toxicity in the non-target species, Lytechinus variegatus. Society for Integrative and Comparative Biology, San Diego, California. 2005.
- Satyamurti ST. The Mollusca of Krusadai Island, Gulf of Mannar. Bull. Madras Govt. Museum (Natural History). 1952;1(2):201.
- Satyamurti T. The mollusca of Krusadai Island (in Gulf of Mannar). Scaphopoda, Pelecypoda and Cephalophoda. Bulletin Madras Government Museum New Serious. 1956;2(1):1-202.
- Stork NE. Measuring Global Biodiversity and Its Decline, in Reaka-Kudla ML, Wilson DE, Wilson EO. (eds.) Biodiversity II: Understanding and Protecting Our Biological Resources, Washington DC: Joseph Henry Press. 1997.
- Strickland JDH, Parsons TR. A practical handbook of seawater analysis. Fishery Research Board of Canada. 1972:310.
- Subba Rao NV, Dey A. Composition and distribution of marine molluscs of Andaman and Nicobar Islands. Journal of the Andaman Science Association. 1991;4:61-66.
- Subba Rao NV. Indian sea shells. (Part 1.) Polyplacophora and gastropods. Kolkata: Zoological Survey of India (Books). 2003:20-337.
- Subrahmanyam TV, Karandikar KR, Murti NN. The marine gastropoda of Bombay. Journal of University of Bombay. 1951;20(3):26-73.
- Takashi N. Spatial hierarchical approach in community ecology: a way beyond high context-dependency and low predictability in local phenomena. Population Ecology. 2004;46(2):105-117.
- Terlizzi A, Fraschetti S, Guidetti P, Boero F. The effects of sewage discharge on shallow hard bottom sessile assemblage. Marine Pollution Bulletin. 2002;44(6):544-550.
- Venkatraman C, Venkataraman K. Diversity of Molluscan fauna along the Chennai coast. International day for biological diversity. 2012:29-35.
- Vladica MS, Snezana S. Use of river macro benthos of Siberia to formulate a biotic index. Hydrobiologia. 1999;392:263-272.
- Walkley A, Armstrong BI. An examination of the degtjareff method for determination of soil organic matter, and a proposed modification of the chromic acid titration. Soil Science. 1934;37(1):29-38.
- Whittaker RH. Vegetation of the Siskiyou Mountains, Oregon and California. Ecological Monographs. 1960;30(3):279-338.
- Whittaker RH. Evolution and measurement of species diversity. Taxon. 1972;21(2):213-251.





