Agricultural Science Digest

  • Chief EditorArvind kumar

  • Print ISSN 0253-150X

  • Online ISSN 0976-0547

  • NAAS Rating 5.52

  • SJR 0.176, CiteScore: 0.357

Frequency :
Bi-monthly (February, April, June, August, October and December)
Indexing Services :
BIOSIS Preview, Biological Abstracts, Elsevier (Scopus and Embase), AGRICOLA, Google Scholar, CrossRef, CAB Abstracting Journals, Chemical Abstracts, Indian Science Abstracts, EBSCO Indexing Services, Index Copernicus

Seasonal Trends of Freshwater Gastropods in Relation to Physicochemical Variables in the Upper Brahmaputra Basin, Assam, India

James Sanong1, Devid Kardong1, Jyotish Sonowal2,*
  • 0000-0001-5971-3775
1Department of Life Sciences, Dibrugarh University, Dibrugarh-786 004, Assam, India.
2Centre for Biotechnology and Bioinformatics, Dibrugarh University, Dibrugarh-786 004, Assam, India.

Background: Limited scientific exploration and documentation have been conducted on the diversity, morphology, physiology, biochemical characteristics and nutritional value of gastropods in this region. The study attempts to present an outline of freshwater gastropods and highlight the significance of physicochemical variables in clarifying their distribution patterns in the upper Brahmaputra Basin of Assam.

Methods: Nine physicochemical parameters were analyzed across 20 sampling stations in four seasons: Pre-monsoon, monsoon, post-monsoon and winter, over three consecutive years, from 2022 to 2024. The Quadrat sampling method (quadrat size-1m2) was followed by taking 10 random sampling sites in each sampling station for sampling across different stations. Diversity indices, principal component analysis (PCA), canonical correspondence analysis (CCA) and linear regression analysis were performed to explore the correlations between physicochemical parameters, sampling stations and freshwater gastropod assemblage.

Result: A total of 16,124 gastropod samples were collected, representing 18 species from three orders-Archaetaenioglossa, Sorbeoconcha and Hygrophila-and six families-Viviparidae, Ampullaridae, Thiaridae, Pachychilidae, Lymnaeidae and Planorbidae. One-way ANOVA substantiated that multiple physicochemical parameters were considerably distinct and Pearson correlation coefficients showed mild to strong links with the distribution of gastropods. Strong positive correlations were found for pH (r = 0.55), DO (r = 0.64) and TA (r = 0.75), while chloride content showed a negative connection (r = -0.30). Principal component analysis (PCA) and canonical correspondence analysis (CCA) revealed that pH, DO, TDS, TA and TH all play important roles in influencing gastropod distribution.

The Brahmaputra river basin, with its vast habitat diversity and varied microclimates, hosts endemic freshwater mollusc species (Bolotov et al., 2024; Sonowal et al., 2021; Kardong et al., 2016; Budha et al., 2010). This basin is bestowed with range of habitats such as streams, wetlands, seagrass meadows and oxbow lakes. The diversity and richness of species in an aquatic ecosystem are influenced by factors such as resource availability, habitat structure and physicochemical properties as well as other factors affecting species dispersal and colonization (Kohler et al., 2012). Temperature, dissolved oxygen, pH and salinity are the chief factors that mould the composition, distribution and abundance of gastropods and to evaluate the functionality of an ecosystem, monitoring these variables is essential (Salawu et al., 2014). It has been observed that some physicochemical parameters influence the distribution and abundance of molluscan populations in Poba Reserve, Assam, India (Chutia and Kardong, 2021).
       
Gastropods are highly diversified class of phylum Mollusca that includes a broad taxonomic group of invertebrates (Lydeard et al., 2004). They occupy a pivotal position in the food chain and it is known to configure the benthic macroinvertebrates (Strong et al., 2008). Many freshwater gastropods are highly sensitive to pollutants and human impact on aquatic ecosystems, making them valuable indicators of biodiversity and ecosystem health (Bogan et al., 2008). In northeastern India, freshwater ecosystems face threats from pollution, dam construction and habitat destruction. Additionally, various freshwater gastropod species have served as traditional food sources for indigenous communities in the Northeast. Certain snail gastropods serve as intermediate hosts for various parasitic diseases that affect both livestock and humans (Alam et al., 2010). Despite their critical ecological significance, limited scientific research has been conducted on freshwater molluscs in the northeast region (Kardong et al., 2016). It was reported that the studies on freshwater molluscs are restricted mostly to diversity, distribution and nutritional values, but the studies are confined to the southern peninsula as well as the Indo-Burma region (Budha, 2005; Ramesha et al., 2013; Subavathy, 2020; Jesintha et al., 2022). Despite the ecological and cultural significance of freshwater gastropods in the Brahmaputra River basin, there is a lack of comprehensive studies on their distribution and response to environmental changes. This study aims to assess the distribution and habitat preferences of freshwater molluscs in the Brahmaputra basin, with a focus on understanding how physicochemical parameters influence their populations.
Sampling
 
20 distinct sampling stations were established across various major aquatic bodies in the upper Brahmaputra basin of Assam (Fig 1). Within each station, 10 random sampling sites were selected for sampling. The Quadrat method (quadrat size-1m2) was followed for sampling. The sampling was carried out during four different seasons: pre-monsoon, monsoon, post-monsoon and winter, over three consecutive years: 2022 to 2024.

Fig 1: Map of study area with co-ordinates.


 
Collection of samples and laboratory analysis
 
Large samples were handpicked, while a Surber net sampler with a mesh size of 0.5-1 mmwas used for smaller samples. The collected samples were sorted into representative morphotypes and their quantities were recorded before being transported to the laboratory for further examination. Water samples from each sampling site were collected seasonally using Tarsons PP/HDPE-100 containers to assess nine different physicochemical variables: pH, water temperature (WT), free carbon dioxide (FCO2), dissolved oxygen (DO), total alkalinity (TA), total dissolved solids (TDS), total hardness (TH), chloride content (Cl-) and nitrate content (NC). pH was measured with a digital pH meter and water temperature was measured with a mercury bulb thermometer. The remaining variables were analyzed according to APHA standards (Sorensen, 2007).
 
Identification
 
The morphological identification of the collected specimens was done following Preston, 1915; Subba Rao, 1989; Ramakrishna and Dey, 2007 and the literature available in the molluscabase.org.
 
Statistical analysis
 
A one-way ANOVA was conducted using GraphPad Prism 8 software to assess the significance of differences in physicochemical variables. Diversity indices, principal component analysis (PCA) and canonical correspondence analysis (CCA) were performed with paleontological statistics software (PAST version 4.03) to explore the correlations between physicochemical parameters, sampling stations and gastropods. Linear regression analysis was employed to evaluate the relationship between physicochemical variables and taxa richness by using GraphPad Prism 8 software and MS-Excel. During this process, variables with insignificant p-values were progressively removed from the regression model, leaving only those variables that were significantly related to taxa richness (p<0.05).
Effects of physicochemical variables on the distribution pattern of freshwater gastropods
 
The One-way ANOVA of nine variables were carried out to check the significant difference at p<0.05 (Table 1). The present study detailed the particulars of the influence of physicochemical parameters on the seasonal distribution pattern of gastropods along the upper Brahmaputra basin. The study recorded the highest pH value of 8.36±0.2 during the monsoon season at sampling station MB and the lowest pH value of 6.9±0.5 at KB and SN during post-monsoon, with an average pH value of 7.59±0.12 across all the stations. A significant difference was observed in pH, p = 0.04 at all sampling stations and the Pearson coefficient (r)= 0.55, which infers that gastropods can endure reasonable pH variations and this result coincides with the previous finding as noted by Dodiya and Poriya (2024).

Table 1: Range of physicochemical parameters across different sampling stations with Pearson correlation coefficients (p-value<0.05 indicates significance).


       
The essence of water temperature in the growth and development of a macro-benthic organism in an aquatic ecosystem can be understood from the study of Nirar and Valparai (2017). The present study recorded maximum WT at MSB (31.4oC±0.5) during the monsoon and the minimum was recorded at TB (18.1oC±0.7) during winter, resulting in a mean temperature of (27.09±0.18). The observations of the present study are consistent with the result of Vase et al., (2018), which recorded maximum temperature during summer and lowest during winter. The recent study recorded a statistically significant difference of p<0.0001 in temperatures in all the twenty sampling stations and Pearson coefficient (r) value of 0.49, which indicates a moderate correlation between the two.
       
DO was recorded highest at JB during the monsoon and lowest at DR during winter with, a mean value of 8.74±0.2. The collective consequence of higher wind rate, heavy precipitation, freshwater influx, influence of deposits and high biological activity (Garg et al., 2009) are the reasons for high values observed during monsoon. The Pearson coefficient (r)=0.64 value indicates a moderate positive correlation with the gastropod community, which is in accordance with Satheeshkumar and Khan (2012). The TDS were highest at OB and lowest at BB during pre-monsoon, with a mean value of 186.15±0.8. The p-value = 0.009 was statistically significant and the Pearson coefficient (r) = 0.57 implies moderate positive correlation with the gastropod community, which is in accordance with the results as detailed by PIP (1987).
       
TA was highest at MSB (68±0.18) during pre-monsoon and lowest at BDR (19.4±0.72) during monsoon, with an average of 44.87±1.6 during pre-monsoon. The reason for the elevated values of DO during the pre-monsoon season may be due to increased biological activity, decreased dilution and evaporation concentration. During the study, significant difference in p value = 0.04 was observed and TA was found to have strong positive correlation with the gastropod population with Pearson coefficient (r = 0.75), which is parallel with the finding as documented by Hoverman et al., (2011). Maximum chloride content was recorded at SR (32.4±1.2), (38.5±1.5) and (40.5±0.9) during pre-monsoon, post-monsoon and winter, respectively, while during monsoon it was recorded highest at MB (31.4±0.5). Minimum value was recorded at BFB (1.4±0.2), (2.5±0.8), (3.2±0.5) and (5.8±1.1) throughout the four seasons with a mean value of (16.33±1.5). Recorded P value = 0.03. The present study showed that chloride content was found to be negatively correlated (r = -30), which coincides with previous studies which have shown that high concentration of chloride has negative effect on unionid mussels, particularly, glochidia (Gills, 2011). The maximum total hardness (TH) was recorded at MB (234.5±0.6) and the lowest at SB (91.4±85), with average values of (151.14±4.6) and p value=0.04, during pre-monsoon and winter, respectively. The recorded Pearson coefficient (r)=0.70 during the study period shows a strong positive correlation with the gastropod population. Some previous findings on the effect of total hardness on gastropods distribution conform with the present result, excluding the findings as documented by Strzelec (2014). P values for free carbon dioxide and nitrate content were found to be insignificant and they were discarded from further analysis and discussion.
 
Abundance and density
 
A total of 16,124 specimens of freshwater gastropods were collected across four seasons from 20 different sampling stations over two years. The study identified 18 species of freshwater gastropods from six families across the various sampling stations throughout the different seasons (Table 2  and Fig 2). During the study period, it was found that throughout the four seasons, the abundance of Filopaludina bengalensis was recorded highest: Pre-monsoon (1.86±0.12), monsoon (0.76±0.21), post-monsoon (2.1±0.0.06) and winter (2.1±0.0.06) with mean value of 1.73±0.48, while Mekongia crassa was recorded lowest during the pre-monsoon (0.33±0.11) and winter (0.26+0.12) with mean value of 0.46±0.04. During monsoon and post-monsoon, the lowest values were recorded with Tarebia lineata (0.11±0.09 and 0.18±0.06, respectively) among all the recorded species.

Table 2: Seasonal variation of abundance and density (pre-monsoon, monsoon, post-monsoon and winter).



Fig 2: Shells of some of the recorded freshwater gastropods from Upper Brahmaputra Basin (dorsal and ventral view).


       
Density was recorded highest with Filopaludina bengalensis (1.43±0.32), (1.22±0.15), (1.58±0.02) during pre-monsoon, post-monsoon and winter, respectively, while Pila globosa was recorded maximum (2.1±0.3) during monsoon and it was recorded lowest with Idiopoma dissimilis (0.14±0.02), Gyraulus convexiusculus (0.06±0.01, Tarebia lineata (0.11±0.02), respectively, among all the recorded species. Density was recorded highest with Filopaludina bengalensis (1.43±0.32), (1.22±0.15), (1.58±0.02) during pre-monsoon, post-monsoon and winter, respectively, while Pila globosa was recorded maximum (2.1±0.3) during monsoon and it was recorded lowest with Idiopoma dissimilis (0.14±0.02), Gyraulus convexiusculus (0.06±0.01), Tarebia lineata (0.11±0.02) and Mekongia crassa (0.17±0.05) during pre-monsoon, monsoon, post-monsoon and winter, respectively. Increase in water temperature, pH, dissolved oxygen, alkalinity and dissolved solids was correlated with high occurrence of density and abundance (Bath and Dhillon, 1999). The collective consequence of the alkaline nature of water, dissolved oxygen, chloride content and dissolved solids might be ascribed to the present study on the richness of gastropods, which afford them an upright habitat to dwell in. During the study period, the seasonal values of abundance and density were found to be statistically significant, where p=0.0003 (abundance) and p = 0.0002 (density).
       
Taxa richness (S), Simpson index (1-D) and Shannon-Weiner index (H) were highest at MB (12±2.10), (0.90±0.02) and (2.4±0.14) during pre-monsoon; (8±0.82), (0.88±0.05) and (2.18±0.24) during monsoon; (13±1.5), (0.91±0.05) and (2.48±0.53) during post-monsoon; and (14±1.3), (0.92±0.14) and (2.59±0.52) during winter respectively (Table 3). The lowest taxa richness (S) was observed at BMB, AB, SN and SB with (1.25±0.6), (1±0.27), (1±0.6), (2±0.5) during pre-monsoon, monsoon, post-monsoon and winter, respectively. The Simpson index(1-D) and Shannon-Weiner index (H) and Shannon-Weiner index (H) were count least at SN with (0.29±0.07), (0.14±0.09), (0.33±0.07), (0.43±0.05) and (0.43±0.18), (0.20±0.05), (0.51±0.2), (0.62±0.7) during pre-monsoon, monsoon, post-monsoon and winter respectively (Table 3).

Table 3: Diversity indices among the (pre-monsoon, monsoon, post-monsoon and winter).


       
The present study found a pattern of low species diversity during monsoon and high diversity during pre-monsoon, post-monsoon and winter across the sampling stations, which is in accordance with previous studies (Raut et al., 2005). Maximum diversity and richness during pre-monsoon, post-monsoon and winter may be due to steady physicochemical variables such as pH, WT, DO, TA and TDS during these seasons. Earlier observation (Field et al., 1982) noted that diversity of a species is governed chiefly by the variations of physicochemical variables, wherein the present observations conform with it. The scatter plot diagram of PCA (Fig 3) depicts that the sampling stations are of different environmental conditions since there is no overlapping of the physicochemical variables. It can be drawn from the ordination diagram (Fig 4) that P. globosa, R. ovalior, I. dissimilis, A. microchaetophora, I. umbilicalis were associated with moderate to high concentration of pH, DO and TA than other physicochemical variables, whereas B. costula, P. olea, A. oxytropis, F. bengalensis and F. micron flourished under high concentration of TH and TDS. Furthermore, M. scabra, M. tuberculata and T. lineata were linked to WT.  It was found that out of the seven physicochemical variables, the taxa richness was negatively correlated to chloride content (R2 = 23%, p = 0.0001; Fig 5), which conforms with the finding as documented by (Uttam et al., 2022), while the rest are positively correlated.

Fig 3: Scatter plot of PCA using seven statistically significant physicochemical variables of water: pH, WT, DO, Cl¯, TA, TH and TDS.



Fig 4: Ordination diagram of physicochemical variables and taxa richness.



Fig 5: Linear regression equation for the (k) pH (l) DO (m) TA (n) TDS (o) TH (p) Cl- (q) WT.

The current study highlights the significance of environmental factors in determining freshwater gastropod abundance and dispersion. Different gastropod species exhibited varying levels of tolerance to specific physico-chemical conditions. Findings revealed that freshwater gastropods diversity and distribution in the upper Brahmaputra basin are influenced by a combination of factors, with species-specific responses. Key parameters affecting these patterns included water temperature (WT), pH, dissolved oxygen (DO), chloride (Cl-), total alkalinity (TA), total hardness (TH) and total dissolved solids (TDS). Our study revealed that the sampling stations SR, BDR and AB had high concentrations of chloride ions, which could explain the reduced taxa richness and densities at these locations. Moreover, linear regression analysis showed no significant relationship between taxa richness and taxa density.
The authors are thankful to the Department of Life Sciences, Centre for Biotechnology and Bioinformatics, Dibrugarh University, Assam, India, for providing the necessary facilities and UGC for the financial support to carry out the research work.
 
Disclaimer
 
The views expressed in this article are solely those of the authors and may not reflect their affiliated institutions. Accuracy is ensured, but no liability is accepted for any losses resulting from the use of the manuscript.
 
Authors’ contributions
 
This work was carried out in collaboration between the three authors. Author JS1 originated the research ideas, drafted the manuscript and analyzed and interpreted the data. Author(s) DK1 and JS2 did the idea formulation, data analysis and reviewed and edited the manuscript. The three authors read and finalized the manuscript.
 
The authors declare that there are no conflicts of interest regarding the publication of this article.

  1. Alam, H.M., Kaur, A., Singh, N.K., Haque, M. and Rath, S.S. (2010). Molluscicidal effects of methanolic extract of Azadirachta indica (NEEM) on snails Lymnaea auricularia and Indo- planorbis exustus. Indian Journal of Animal Research. 44(3): 178-182.

  2. Bath, K.S., Kaur, H. and Dhillon, S.S. (1999). Correlation of molluscs with physico-chemical factors at Harike Reservoir (Punjab). Indian Journal of Environmental Sciences. 3(2): 159-163.

  3. Bogan, A.E. and Roe, K.J. (2008). Freshwater bivalve (Unioniformes) diversity, systematics and evolution: Status and future directions. Journal of the North American Benthological Society. 27(2): 349-369.

  4. Bolotov, I. N., Sonowal, J., Kardong, D., Pasupuleti, R., Subba Rao, N.V., Unnikrishnan, S.K. and Vikhrev, I.V. (2024). Discovery of an endemism hotspot of freshwater mussels (Bivalvia: Unionidae) in Assam, with a description of two new genera. Zoological Journal of the Linnean Society. 202(4): zlae052.

  5. Budha, P.B. (2005). Nepalese malacology trails behind. 3(5): 9-10.

  6. Budha, P.B., Aravind, N.A. and Daniel, B.A. (2010). The status and distribution of freshwater molluscs of the eastern Himalaya. In: Allen, D.J., Molur, S. and Daniel, B.A. (Compilers), The Status and Distribution of Freshwater Biodiversity in the Eastern Himalaya. 42-53. IUCN, Cambridge, UK and Gland, Switzerland and Zoo Outreach Organization, Coimbatore, India. 88.

  7. Chutia, J. and Kardong, D. (2021). Current status and seasonal distribution of malacofaunal assemblage in poba reserve forest in relation to certain physico-chemical parameters. Asian Journal of Biological and Life Sciences. 10(1): 93-100.

  8. Dodiya, D. and Poriya, P. (2024). Correlating distribution patterns of intertidal gastropods with physicochemical parameters along the Adri Coast of Gujarat, India. European Journal of Theoretical and Applied Sciences. 2(3): 235-243.

  9. Field, J.1., Clarke, K.R. and Warwick, R.M. (1982). A practical strategy for analysing multispecies distribution patterns. Marine Ecology Progress Series. pp: 37-52.

  10. Garg, R.K., Rao, R.J. and Saksena, D.N. (2009). Correlation of molluscan diversity with physico-chemical characteristics of water of Ramsagar reservoir, India. International Journal of Biodiversity and Conservation. 1(6): 202-207.

  11. Gills, P.L. (2011). Assessing the toxicity of sodium chloride to the glochidia of freshwater mussels: Implications for salinization of surface waters. Environmental Pollution. 159(6): 1702- 1708.

  12. Hoverman, J.T., Davis, C.J., Werner, E.E., Skelly, D.K., Relyea, R.A. and Yurewicz, K.L. (2011). Environmental gradients and the structure of freshwater snail communities. Ecography. 34(6): 1049-1058.

  13. Jesintha, N., Jayakumar, N., Karuppasamy, K., Ahilan, B., Manikandavelu, D., Uma, A. and Madhavi, K. (2022). An annotated check- list of finfish and shellfish diversity of Pulicat Lake, Southeast Coast of India. Indian Journal of Animal Research. 56(4): 468-475. doi: 10.18805/IJAR.B-4740.

  14. Kardong, D., Puzari, M. and Sonowal, J. (2016). Diversity of freshwater mollusc in Maguri Beel: A floodplain wetland of Tinsukia district in Assam, India. International Journal of Current Research. 8(4): 29169-29176.

  15. Köhler, F., Seddon, M., Bogan, A.E., Tu, D.V., Sri-Aroon, P., Allen, D., Allen, D.J., Smith, K.G. and Darwall, W.R.T. (2012). The status and distribution of freshwater molluscs of the Indo-Burma region. In: The status and distribution of freshwater biodiversity in Indo-Burma. pp: 66-88.

  16. Lydeard, C., Cowie, R.H., Ponder, W.F., Bogan, A.E., Bouchet, P., Clark, S.A., Cummings, K.S., Frest, T.J., Gargominy, O., Herbert, D.G. and Hershler, R. (2004). The global decline of nonmarine mollusks. BioScience. 54(4): 321-330.

  17. Nirar, D. and Valparai, C.D. (2017). Gastropod diversity with physico-chemical characteristics of water and soil in selected areas of Dakshina Kannada district of Karnataka, India.

  18. PIP, E. (1987). Species richness of freshwater gastropod communities in central North America. Journal of Molluscan Studies. 53(2): 163-170.

  19. Preston, H.B. (1915). The fauna of british India including Ceylon and Burma. Taylor and Francis, Red Lion Court Fleet Street; Bombay.

  20. Ramakrishna and A. Dey (2007). Handbook on Indian Freshwater Molluscs. Zoological Survey of India, Kolkata. pp: 399. 

  21. Ramesha, M.M., Sophia, S. and Muralidhar, M. (2013). Freshwater bivalve fauna in the Western Ghats rivers of Karnataka, India: Diversity, distribution patterns, threats and conservation needs. International Journal of Current Research. 5: 2500-2505.

  22. Raut, D., Ganesh, T., Murty, N.V.S.S. and Raman, A.V. (2005). Macrobenthos of kakinada bay in the Godavari delta, East coast of India: Comparing decadal changes. Estuarine, Coastal and Shelf Science. 62(4): 609-620.

  23. Salawu, O.T. and Odaibo, A.B. (2014). The bionomics and diversity of freshwater snails’ species in Yewa North, Ogun State, Southwestern Nigeria. Helminthologia. 51: 337-344.

  24. Satheeshkumar, P. and Khan, A.B. (2012). Influence of environmental parameters on the distribution and diversity of molluscan composition in Pondicherry mangroves, southeast coast of India. Ocean Science Journal. 47: 61-71.

  25. Sonowal, J., Puzari, M. and Kardong, D. (2021). Diversity of freshwater molluscs from the upper Brahmaputra Basin, Assam, India. Journal of Threatened Taxa. 13(5): 18237- 18246.

  26. Sorensen, T.D. (2007). Report of the 2007 APHA house of delegates: Actions of the official legislative body of the American pharmacists association. Journal of the American Pharmacists Association. 47(5): 580-582.

  27. Strong, E.E., Gargominy, O., Ponder, W.F. and Bouchet, P. (2008). Global diversity of gastropods (Gastropoda; Mollusca) in freshwater. Freshwater Animal Diversity Assessment. 149-166.

  28. Strzelec, M., Krodkiewska, M. and Królczyk, A. (2014). The impact of environmental factors on the diversity of gastropod communities in sinkhole ponds in a coal mining region (Silesian Upland, Southern Poland). Biologia. 69: 780-789.

  29. Subavathy, P. (2020). Histological investigation of the digestive system and SEM study of radula in fusinus nicobaricus (Gastropoda: Fasciolariidae). Indian Journal of Animal Research. 54(2): 191-195.  doi: 10.18805/ijar.B-3759.

  30. Subba Rao, N.V. (1989). Handbook, freshwater molluscs of India.

  31. Vase, V.K., Dash, G., Sreenath, K.R., Temkar, G., Shailendra, R., Mohammed Koya, K., Divu, D., Pradhan, R.K., Sukhdhane, K.S. and Jayasankar, J. (2018). Spatio-temporal variability of physico-chemical variables, chlorophyll a and primary productivity in the northern Arabian Sea along India coast. Environmental Monitoring and Assessment. 190: 1-14.

Editorial Board

View all (0)