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Copepod carcasses in the western Bay of Bengal and associated ecology

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Abstract

Although a portion of all copepods in the natural environment are physiologically inactive or dead, there is little data on this aspect in Indian seas. Using the classical neutral red live staining technique, the dead percentage of copepods in the western Bay of Bengal (BoB) is determined for the first time in this study, which takes into account hydrography and zooplankton samples collected on April 2015 (Spring Intermonsoon [SIM]) from 6 inshore and 8 offshore locations in the western BoB. The offshore parts of the research area were infested with a persistent and extensive warm-core eddy/gyre during the sampling time, as demonstrated by satellite data of sea surface temperature, mean sea level anomaly, and surface currents. As a result, the mixed layer depth in the offshore zone was higher, whereas nutrients, chlorophyll a, and turbidity were significantly lower than inshore. Copepods dominated the zooplankton community (> 80%), with abundances ranging from 112 to 2580 No m−3 in the study area. Calanoids (particularly Paracalanidae) dominated nearshore waters (35–65%), whereas cyclopoids (notably Corycaeidae and Oncaeidae) dominated offshore (49–71%). There were 48 species of copepods identified in total, and all of them had dead individuals (carcasses). Offshore waters had a larger percentage of copepod carcasses (27–39%) than inshore seas (18–28%). The larger percentage of carcasses is possibly related to a higher top-down feeding pressure on cyclopoids in offshore waters due to extreme oligotrophy and the dominance of the microbial food web.

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Availability of data and materials

The data sets used and/or analysed during the current study are available from the corresponding author on reasonable request through the Director, CSIR-National Institute of Oceanography, or the Scientist-in-Charge, Regional Centre Kochi.

References

  • Anjusha, A., Jyothibabu, R., Jagadeesan, L., Mohan, A. P., Sudheesh, K., Krishna, K., Ullas, N., & Deepak, M. P. (2013). Trophic efficiency of plankton food webs: Observations from the Gulf of Mannar and the Palk Bay, Southeast Coast of India. Journal of Marine Systems, 115, 40–61.

    Google Scholar 

  • Arunpandi, N., Jyothibabu, R., Jagadeesan, L., Gireeshkumar, T. R., Karnan, C., & Naqvi, S. A. (2017). Noctiluca and copepods grazing on the phytoplankton community in a nutrient-enriched neashore environment along the southwest coast of India. Environmental Monitoring and Assessment, 189(7), 351.

    CAS  Google Scholar 

  • Arunpandi, N., Jyothibabu, R., Jagadeesan, L., Parthasarathi, S., Anjusha, A., & Albin, K. J. (2021). Impact of human-altered hydrographical setting on the copepod community structure in an extensive tropical estuary along the southwest coast of India. Oceanologia, 63(1), 115–132. https://doi.org/10.1016/j.oceano.2020.10.004

    Article  Google Scholar 

  • Bickel, S. L., Tang, K. W., & Grossart, H. P. (2009). Use of aniline blue to distinguish live and dead crustacean zooplankton composition in freshwaters. Freshwater Biology, 54(5), 971–981.

    Google Scholar 

  • Bottger-Schnack, R. (1996). Vertical structure of small metazoan plankton, especially non-calanoid copepods. 1. Deep Arabian Sea. Journal of Plankton Research, 18, 1073–1101.

    Google Scholar 

  • Cervetto, G., Gaudy, R., & Pagano, M. (1999). Influence of salinity on the distribution of Acartiatonsa (Copepoda, Calanoida). Journal of Experimental Marine Biology and Ecology, 239(1), 33–45.

    Google Scholar 

  • Chen, G., Wang, D., & Hou, Y. (2012). The features and interannual variability mechanism of mesoscale eddies in the Bay of Bengal. Continental Shelf Research, 47, 178–185.

    Google Scholar 

  • Conway, D. V. P., White, R. G., Hugues-Dit-Ciles, J., Gallienne, C. P., & Robins, D. B. (2003). Guide to the coastal and surface zooplankton of the South-Western Indian Ocean. Occasional Publication of the Marine Biological Association of the United Kingdom, No. 15, Plymouth, UK, p. 354.

  • Daase, M., Varpe, O., & Falk-Petersen, S. (2014). Non-consumptive mortality in copepods: Occurrence of Calanus spp. carcasses in the Arctic Ocean during winter. Journal of plankton research36(1), pp.129–144.

  • Deevey, G. B., & Brooks, A. L. (1971). Annual cycle in quantity and composition of zooplankton of Sargasso Sea off Bermuda 2. Surface to 2,000 m. Limnology and Oceanography, 16, 927–943.

    Google Scholar 

  • Elliott, D. T., & Tang, K. W. (2009). Simple staining method for differentiating live and dead marine zooplankton in field samples. Limnology and Oceanography: Methods, 7(8), 585–594.

    Google Scholar 

  • Elliott, D. T., & Tang, K. W. (2011a). Spatial and temporal distributions of live and dead copepods in the lower Chesapeake Bay (Virginia, USA). Estuaries and Coasts, 34(5), 1039–1048.

    Google Scholar 

  • Elliott, D. T., & Tang, K. W. (2011b). Influence of carcass abundance on estimates of mortality and assessment of population dynamics in Acartia tonsa. Marine Ecology Progress Series, 427, 1–12.

    Google Scholar 

  • Elliott, D. T., Pierson, J. J., & Roman, M. R. (2013). Copepods and hypoxia in Chesapeake Bay: Abundance, vertical position and nonpredatory mortality. Journal of Plankton Research, 35, 1027–1034.

    CAS  Google Scholar 

  • Fernandes, V. (2008). The effect of semi-permanent eddies on the distribution of mesozooplankton in the central Bay of Bengal. Journal of Marine Research, 66(4), 465–488.

    Google Scholar 

  • Fernandes, V., & Ramaiah, N. (2014). Distributional characteristics of surface-layer mesozooplankton in the Bay of Bengal during the 2005 winter monsoon. Indian Journal of Marine Sciences, 43(2), 176–188.

    Google Scholar 

  • Gauns, M., Madhupratap, M., Ramaiah, N., Jyothibabu, R., Fernandes, V., Paul, J. T., & Prasannakumar, S. (2005). Comparative accounts of biological productivity characteristics and estimates of carbon fluxes in the Arabian Sea and Bay of Bengal. Deep Sea Research II, 52, 2003–2017.

    Google Scholar 

  • Genin, A., Gal, G., & Haury, L. (1995). Copepod carcasses in the ocean. II. Near coral reefs. Marine ecology progress series. Oldendorf, 123(1), 65–71.

  • Go, Y.B., Oh, B.C., & Terazaki, M. (1998). Feeding behavior of the poecilostomatoid copepods Oncaea spp. on chaetognaths. Journal of Marine Systems, 15(1–4), pp.475–482.

  • Gomez-Gutierrez, J., Peterson, W. T., De Robertis, A., & Brodeur, R. D. (2003). Mass mortality of krill caused by parasitoid ciliates. Science, 301(5631), 339–339.

    CAS  Google Scholar 

  • Grasshoff, K. (1983). Methods of seawater analysis. In: K. Grasshoff, Ehrhardt, M., Kremling, K., (eds.) Weinheim, Verlag Chemie, pp. 89–224.

  • Hall, L. W., Ziegenfuss, M. C., Anderson, R. D., & Killen, W. D. (1995). Use of estuarine water column tests for detecting toxic conditions in ambient areas of the Chesapeake Bay watershed. Environmental Toxicology and Chemistry, 14(2), 267–278.

    CAS  Google Scholar 

  • Hansen, F. C., & Van Boekel, W. H. M. (1991). Grazing pressure of the calanoid Copepod Temora Iongicorm’s on a Phaeocystis dominated spring. Marine Ecology Progress Series, 78, 123–129.

    Google Scholar 

  • Haury, L., Fey, C., Gal, G., Hobday, A., & Genin, A. (1995). Copepod carcasses in the ocean. I. Over seamounts. Marine ecology progress series. Oldendorf, 123(1), 57–63.

  • Hirst, A. G., & Kiorboe, T. (2002). Mortality of marine planktonic copepods: Global rates and patterns. Marine Ecology Progress Series, 230, 195–209.

    Google Scholar 

  • Homma, T., & Yamaguchi, A. (2010). Vertical changes in abundance, biomass and community structure of copepods down to 3000 m in the southern Bering Sea. Deep-Sea Res Part I, 57, 965–977.

    Google Scholar 

  • Ittekkot, V., Nair, R. R., Honjo, S., Ramaswamy, V., Bartsch, M., Manganini, S., & Desai, B. N. (1991). Enhanced particle fluxes in Bay of Bengal induced by injection of fresh water. Nature, 351(6325), 385–387.

    Google Scholar 

  • Jagadeesan, L., Jyothibabu, R., Anjusha, A., Mohan, A. P., Madhu, N. V., Muraleedharan, K. R., & Sudheesh, K. (2013). Ocean currents structuring the mesozooplankton in the Gulf of Mannar and the Palk Bay, southeast coast of India. Progress in Oceanography, 110, 27–48.

    Google Scholar 

  • Jagadeesan, L., Jyothibabu, R., Arunpandi, N., Karnan, C., & Balachandran, K. K. (2017). Dominance of coastal upwelling over mud bank in shaping the mesozooplankton along the southwest coast of India during the southwest monsoon. Progress in Oceanography, 156, 252–275.

    Google Scholar 

  • Jagadeesan, L., & Jyothibabu, R. (2016). Tumour-like anomaly of copepods-an evaluation of the possible causes in Indian marine waters. Environmental Monitoring and Assessment, 188(4), 244.

    CAS  Google Scholar 

  • Jagadeesan, L., Kumar, G. S., Rao, D. N., & Srinivas, T. N. R. (2019). Role of eddies in structuring the mesozooplankton composition in coastal waters of the western Bay of Bengal. Ecological Indicators, 105, 137–155.

    CAS  Google Scholar 

  • Jyothibabu, R., Madhu, N. V., Maheswaran, P. A., Jayalakshmy, K. V., Nair, K. K. C., & Achuthankutty, C. T. (2008). Seasonal variation of microzooplankton (20–200 μm) and its possible implications on the vertical carbon flux in the western Bay of Bengal. Continental Shelf Research, 28(6), 737–755.

    Google Scholar 

  • Jyothibabu, R., Vinayachandran, P. N., Madhu, N. V., Robin, R. S., Karnan, C., Jagadeesan, L., & Anjusha, A. (2015). Phytoplankton size structure in the southern Bay of Bengal modified by the summer monsoon current and associated eddies: Implications on the vertical biogenic flux. Journal of Marine Systems, 143, 1–63.

    Google Scholar 

  • Jyothibabu, R., Jagadeesan, L., & Lallu, K. R. (2016). Copepod carcasses in a tropical estuary during different hydrographical settings. Environmental Monitoring and Assessment, 188(10), 559.

    Google Scholar 

  • Jyothibabu, R., Arunpandi, N., Jagadeesan, L., Karnan, C., Lallu, K. R., & Vinayachandran, P. N. (2018). Response of phytoplankton to heavy cloud cover and turbidity in the northern Bay of Bengal. Scientific Reports, 8(1), 11282. https://doi.org/10.1038/s41598-018-29586-1

    Article  CAS  Google Scholar 

  • Jyothibabu, R., Karnan, C., Arunpandi, N., Krishnan, S. S., Balachandran, K. K., & Sahu, K. C. (2021). Significantly dominant warm-core eddies: An ecological indicator of the basin-scale low biological production in the Bay of Bengal. Ecological Indicators, 121, p.107016.

  • Karnan, C., Jyothibabu, R., Arunpandi, N., Pandiyarajan, R. S., Parthasarathi, S., & Santhikrishnan, S. (2021). Microplankton size structure induced by a warm-core eddy in the western Bay of Bengal: Role of Trichodesmium abundance. Oceanologia, 63(3), 283–300. https://doi.org/10.1016/j.oceano.2021.02.003

    Article  Google Scholar 

  • Kasturirangan, L.R. (1963). A key for the identification of the more common planktonic copepoda of the Indian coastal waters (No. 2). Council of Scientific & Industrial Research, India.

  • Kimmerer, W. J., & McKinnon, A. D. (1990). High mortality in a copepod population caused by a parasitic dinoflagellate. Marine Biology, 107(3), 449–452.

    Google Scholar 

  • Kirillin, G., Grossart, H. P., & Tang, K. W. (2012). Modeling sinking rate of zooplankton carcasses: Effects of stratification and mixing. Limnology and Oceanography, 57(3), 881–894.

    Google Scholar 

  • Leps, J., & Smilauer, P. (2003). Multivariate analysis of ecological data using CANOCO. Cambridge University Press.

    Google Scholar 

  • Madhu, N. V., Jyothibabu, R., Maheswaran, P. A., Gerson, V. J., Gopalakrishnan, T. C., & Nair, K. K. C. (2006). Lack of seasonality in phytoplankton standing stock (chlorophyll a) and production in the western Bay of Bengal. Continental Shelf Research, 26(16), 1868–1883.

    Google Scholar 

  • Madhupratap, M., Gauns, M., Ramaiah, N., Prasannakumar, S., Muraleedharan, P. M., de Douza, S. N., Sardesai, S., & Usha, M. (2003). Biogeochemistry of Bay of Bengal: Physical, chemical and primary productivity characteristics of the central and western Bay of Bengal during summer monsoon 2001. Deep-Sea Research II, 50, 881–886.

    CAS  Google Scholar 

  • Madhupratap, M., Gopalakrishnan, T. C., Haridas, P., Nair, K. K. C., Aravindakshan, P. N., Padmavati, G., & Paul, S. (1996). Lack of seasonal and geographic variation in mesozooplankton biomass in the Arabian Sea and its structure in the mixed layer. Current Science, 71(11), 863–868.

    Google Scholar 

  • Morales, C. E., Harris, R. P., Head, R. N., & Tranter, P. R. G. (1993). Copepod grazing in the oceanic northeast Atlantic during a 6 week drifting station: The contribution of size classes and vertical migrants. Journal of Plankton Research, 15(2), 185–212.

    Google Scholar 

  • Ohman, M. D., & Wood, S. N. (1995). The inevitability of mortality. ICES Journal of Marine Science: Journal Du Conseil, 52(3–4), 517–522.

    Google Scholar 

  • Postel, L., Fock, H., & Hagen, W. (2000). Biomass and abundance. In ICES zooplankton methodology manual 2000 Jan 1, Academic Press, pp. 83–192.

  • Prasannakumar, S., Muraleedharan, P. M., Prasad, T. G., Gauns, M., Ramaiah, N., de Souza, S. N., Sardesai, S., & Madhupratap, M. (2002). Why is the Bay of Bengal less productive during summer monsoon compared to the Arabian Sea? Geophysical Research Letters, 29(24), 88–91.

    Google Scholar 

  • Rakhesh, M., Raman, A. V., Kalavati, C., Subramanian, B. R., Sharma, V. S., Babu, E. S., & Sateesh, N. (2008). Zooplankton community structure across an eddy-generated upwelling band close to a tropical bay-mangrove ecosystem. Marine Biology, 154(6), 953–972.

    Google Scholar 

  • Roe, H. S. J. (1988). Midwater biomass profiles over the Madeira abyssal plain and the contribution of copepods. Hydrobiologia, 167, 169–181.

    Google Scholar 

  • Roman, M., Smith, S., Wishner, K., Zhang, X., & Gowing, M. (2000). Mesozooplankton production and grazing in the Arabian Sea. Deep Sea Research Part II: Topical Studies in Oceanography, 47(7–8), 1423–1450.

    Google Scholar 

  • Sameoto, D. D. (1986). Influence of the biological and physical environment on the vertical distribution of mesozooplankton and micronekton in the eastern tropical Pacific. Marine Biology, 93, 263–279.

    Google Scholar 

  • Sewell, R. B. S. (1999). The copepoda of Indian seas, 10. Daya Books.

  • Tanaka, O. (1956). The pelagic copepods of the Izu region, Middle Japan. Systematic account. II Families Paracalanidae and Pseudocalanidae.–Publ. Seto Marine Biological Laboratory, 5, 367–406.

    Google Scholar 

  • Tang, K. W., Bickel, S. L., Dziallas, C., & Grossart, H. P. (2009). Microbial activities accompanying decomposition of cladoceran and copepod carcasses under different environmental conditions. Aquatic Microbial Ecology, 57(1), 89–100.

    Google Scholar 

  • Tang, K. W., & Elliott, D. T. (2014). Copepod carcasses: Occurrence, fate and ecological importance. Copepods: Diversity, Habitat and Behavior, pp.255–278.

  • Tang, K. W., Freund, C. S., & Schweitzer, C. L. (2006). Occurrence of copepod carcasses in the lower Chesapeake Bay and their decomposition by ambient microbes. Estuarine, Coastal and Shelf Science, 68(3), 499–508.

    Google Scholar 

  • Tang, K. W., Gladyshev, M. I., Dubovskaya, O. P., Kirillin, G., & Grossart, H. P. (2014). Zooplankton carcasses and non-predatory mortality in freshwater and inland sea environments. Journal of Plankton Research, 36(3), 597–612.

    CAS  Google Scholar 

  • Terazaki, M., & Wada, M. (1988). Occurrence of large numbers of carcasses of the large, grazing copepod Calanus cristatus from the Japan Sea. Marine Biology, 97(2), 177–183.

    Google Scholar 

  • Turner, J. T. (1986). Zooplankton feeding ecology: Contents of fecal pellets of the cyclopoid copepods Oncaea venusta, Corycaeus amazonicus, Oithona plumifera, and O. simplex from the northern Gulf of Mexico. Marine Ecology, 7(4), pp.289–302.

  • Uye, S. (1986). Impact of copepod grazing on the red-tide flagellate Chattonellaantiqua. Marine Biology, 92(1), 35–43.

    Google Scholar 

  • Wu, C. H., Hwang, J. S., & Yang, J. S. (2004). Diets of three copepods (Poecilostomatoida) in the southern Taiwan Strait. Zoological Studies, 43(2), 388–392.

    Google Scholar 

  • Yanez, S., Hidalgo, P., & Escribano, R. (2012). Natural mortality of Paracalanus indicus (Copepoda: Calanoida) in coastal upwelling areas associated with oxygen minimum zone in the Humboldt Current system: Implications for the passive carbon flux. Revista De Biologia Marina y Oceanografia, 47, 295–310.

    Google Scholar 

  • Yamaguchi, A., Watanabe, Y., Ishida, H., Harimoto, T., Furusawa, K., Suzuki, S., Ishizaka, J., Ikeda, T., & Mac Takahashi, M. (2002). Community and trophic structures of pelagic copepods down to greater depths in the western subarctic Pacific (WEST-COSMIC). Deep Sea Research Part I: Oceanographic Research Papers, 49(6), 1007–1025.

    Google Scholar 

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Acknowledgements

The authors appreciate the facilities and support provided by the Director, CSIR-National Institute of Oceanography (CSIR-NIO), India. We are grateful to all of our colleagues at the National Institute of Oceanography in India who assisted us with the fieldwork. This research was conducted as part of the Eastern Offshore Environmental Monitoring project, which was supported by ONGC, IPSHEM, Goa, India. The DST-INSPIRE Fellowship was provided to the first author by the Department of Science and Technology (DST) (IF120804). This is the NIO contribution 6860.

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This study received funding from the ONGC, IPSHEM, Goa, India.

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AN: conceptualisation, investigation, writing—original draft; funding acquisition; project administration; JR: conceptualisation, investigation; visualisation, formal analysis; supervision and funding acquisition; JL: conceptualisation, investigation, visualisation, formal analysis; LS: investigation, visualization, formal analysis; SS: investigation; visualization; BA: investigation; visualisation.

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Correspondence to Jyothibabu R..

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N., A., R., J., L., J. et al. Copepod carcasses in the western Bay of Bengal and associated ecology. Environ Monit Assess 194, 137 (2022). https://doi.org/10.1007/s10661-021-09748-x

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