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Seasonal dynamics of body size in calanoid copepods (Calanoida: Copepoda) from the stressed tropical coast of India, Chennai, Bay of Bengal

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Abstract

Calanoid copepods have gained significant interest due to their rapid response to changes in environment. This study examined the seasonal variation in the size of calanoid copepods and their relationships to various environmental parameters in a tropical coast of India. Zooplankton samples were collected at Marina Beach, India, from January to December 2021. Ten calanoid species were selected based on their distribution to study the seasonal variation in the size, and the results showed a clear seasonal pattern, with smaller size of calanoid observed during summer months with high temperatures and larger sizes during the monsoon season associated with increased rainfall and nutrient availability. Negative correlations were observed between copepod size variation and temperature, while positive correlations were observed with dissolved oxygen, pH, salinity, and chlorophyll-a concentration. Acrocalanus gibber, Acrocalanus gracilis and Canthocalanus pauper showed changes that are more pronounced in body size (0.89–0.99, 1.12–1.23 mm and 1.41–1.52 mm, respectively) indicating species-specific responses to environmental fluctuations. These findings highlight the influence of environmental parameters in determining the size of calanoid copepods in tropical oceans. Moreover, this study contributes to our understanding of the ecological processes and global warming that determine copepod size variation in coastal ecosystems.

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References

  • Almeda R, Gréve GH, Kiørboe T (2017) Behavior is a major determinant of predation risk in zooplankton. Ecosphere 8:1–20. https://doi.org/10.1002/ecs2.1668

    Article  Google Scholar 

  • Altieri AH, Gedan KB (2015) Climate change and dead zones. Glob Change Biol 21(4):1395–1406

    Article  Google Scholar 

  • Boxshall G, Halsey S (2004) An introduction to copepod diversity. The Ray Society, London

    Google Scholar 

  • Castor G, Roger H (1995) Effect of total organic content of eggs on hatching success and naupliar survival in the copepod Calanus helgolandicus. Limnol Oceanogr 40:476–482. https://doi.org/10.4319/lo.1995.40.3.0476

    Article  Google Scholar 

  • Chen Q, Sheng J, Lin Q, Gao Y, Lv J (2006) Effect of salinity on reproduction and survival of the copepod Pseudodiaptomus annandalei Sewell, 1919. Aquaculture 258:575–582. https://doi.org/10.1016/j.aquaculture.2006.04.032

    Article  CAS  Google Scholar 

  • Chew LL, Chong VC (2016) Response of marine copepods to a changing tropical environment: winners, losers and implications. PeerJ 4:2052. https://doi.org/10.7717/peerj.2052

    Article  Google Scholar 

  • Choi SY, Lee EH, Soh HY, Jang MC (2021) Effects of temperature and salinity on egg production, hatching, and mortality rates in Acartia ohtsukai (Copepoda, Calanoida). Front Mar Sci 8:1–9. https://doi.org/10.3389/fmars.2021.704479

    Article  Google Scholar 

  • Dahms HU, Tseng LC, Hsiao SH, Chen QC, Kim BR, Hwang JS (2012) Biodiversity of planktonic copepods in the Lanyang River (Northeastern Taiwan), a typical watershed of Oceania. Zool Stud 51:160–174

    Google Scholar 

  • Drira Z, Belhassen M, Ayadi H, Hamza A, Zarrad R, Bouaïn A, Aleya L (2010) Copepod community structure related to environmental factors from a summer cruise in the Gulf of Gabès (Tunisia, eastern Mediterranean Sea). J Mar Biol Assoc UK 90:145–157. https://doi.org/10.1017/S0025315409990403

    Article  CAS  Google Scholar 

  • Drira Z, Kmiha-Megdiche S, Sahnoun H, Tedetti M, Pagano M, Ayadi H (2018) Copepod assemblages as a bioindicator of environmental quality in three coastal areas under contrasted anthropogenic inputs (Gulf of Gabes, Tunisia). J Mar Biol Assoc UK 98:1889–1905. https://doi.org/10.1017/S0025315417001515

    Article  Google Scholar 

  • Evans LE, Hirst AG, Kratina P, Beaugrand G (2020) Temperature-mediated changes in zooplankton body size: large scale temporal and spatial analysis. Ecography 43:581–590. https://doi.org/10.1111/ecog.04631

    Article  Google Scholar 

  • Gautam KR, Vongvisessomjai S, Kazama S (2000) Sea surface temperature and net heat flux variation in the Gulf of Thailand using Buoy, meteorological and remote sensing data. Coast Eng J 42:341–356. https://doi.org/10.1142/s0578563400000171

    Article  Google Scholar 

  • Hammer O, David AT, Paul DR (2001) PAST: paleontological statistics software package for education and data analysis. Palaeontol Electron 4:1–9

    Google Scholar 

  • Harrison JF, Kaiser A, VandenBrooks JM (2010) Atmospheric oxygen level and the evolution of insect body size. Proc R Soc B 277:1937–1946

    Article  PubMed  PubMed Central  Google Scholar 

  • Henry R, Hino K, Gentil JG, Tundisi JG (1985) Primary production and effects of enrichment with nitrate and phosphate on phytoplankton in the Barra Bonita reservoir (State of São Paulo, Brazil). Internationale Revue Der Gesamten Hydrobiologie Und Hydrographie 70:561–573. https://doi.org/10.1002/iroh.19850700409

    Article  CAS  Google Scholar 

  • Hildrew AGR, Edmonds-brown R (2007) Body size: the structure andfunction of aquatic ecosystems. Ecological Reviews. Cambridge University Press, Cambridge

  • Huntley ME, Lopez MDG (1992) Temperature-dependent production of marine copepods: a global synthesis. Am Nat 140:201–242. https://doi.org/10.1086/285410

    Article  CAS  PubMed  Google Scholar 

  • Irina P, Smith S, Popova E (2012) Calanoid copepods of the Arabian sea region. Sultan Qaboos University Academic Publication Board, Muscat, Sultanate of Oman

    Google Scholar 

  • Jakobsen HH, Markager S (2016) Carbon-to-chlorophyll ratio for phytoplankton in temperate coastal waters: seasonal patterns and relationship to nutrients. Limnol Oceanogr 61:1853–1868. https://doi.org/10.1002/lno.10338

    Article  Google Scholar 

  • Janakiraman A, Naveed MS, Sheriff MA, Altaff K (2016) Meiofaunal response to the tidal exchange and domestic sewage in the Adyar estuary, Chennai, India. Ind J Geo-Mar Sci 45:1341–1348

  • Jennings CD, Greenwood JG, Kay BH (1994) Response of Mesocyclops (Cyclopoida: Copepoda) to biological and physicochemical attributes of rainwater tanks. Environ Entomol 23:479–486. https://doi.org/10.1093/ee/23.2.479

    Article  Google Scholar 

  • Kasturirangan LR (1963) A Key for identification of the most common planktonic copepod of Indian coastal water. In: Panikkar NK (eds), Council of Scientific and Industrial Research, New Delhi

  • Kulkarni SJ (2016) A review on research and studies on dissolved oxygen and its affecting parameters. Inter J Res Rev 3:18–22

  • Landry MR (1978) Predatory feeding behavior of a marine copepod. Limnol Oceanogr 23:1103–1113. https://doi.org/10.4319/lo.1978.23.6.1103

    Article  Google Scholar 

  • Liao CH, Chang WJ, Lee MA, Lee KT (2006) Summer distribution and diversity of copepods in upwelling waters of the Southeastern East China sea. Zool Stud 45:378–394

    Google Scholar 

  • Milione M, Zeng C (2008) The effects of temperature and salinity on population growth and egg hatching success of the tropical calanoid copepod, Acartia sinjiensis. Aquaculture 275:116–123. https://doi.org/10.1016/j.aquaculture.2007.12.010

    Article  Google Scholar 

  • Murphy J, Riley JP (1962) A modified single solution method for the determination of phosphate in natural waters. Anal Chim Acta 27:31–36

    Article  CAS  Google Scholar 

  • Muthurajah SD, Leong SCY, Kuwahara VS, Moh PY, Ross OBH, Yoshida T (2021) Monsoonal and spatial influence on zooplankton variation in a tropical bay, North Borneo, Malaysia. Reg Stud Mar Sci 47:101952. https://doi.org/10.1016/j.rsma.2021.101952

    Article  Google Scholar 

  • Nagaraj M (1992) Combined effects of temperature and salinity on the development of the copepod Eurytemora affinis. Aquaculture 103:65–71

    Article  Google Scholar 

  • Nawaz MA, Sivakumar K, Baskar G, Vijayaraj R (2023a) Diversity rhythm in pontellid copepods (Pontellidae: Copepoda) from the covelong coast pre- and post-COVID-19 lockdown, Bay of Bengal. Turk J Zool 47:71–80. https://doi.org/10.55730/1300-0179.3117

    Article  CAS  Google Scholar 

  • Nawaz MA, Sivakumar K, Baskar G (2023b) Impact of variation in environmental parameters on abundance of Paracalanidae (Calanoida: Copepoda) from the tropical coast of India, Bay of Bengal. Russ J Mar Biol 49(5):391–400

    Google Scholar 

  • Paffenhöfer GA (1984) Food ingestion by the marine planktonic copepod Paracalanus in relation to abundance and size distribution of food. Mar Bio 80:323–333. https://doi.org/10.1007/BF00392828

    Article  Google Scholar 

  • Palanivel PS, Veeraiyan B, Perumal M, Palanichamy S, Rengasamy P (2022) Seasonal carbonate system vis-à-vis pH and salinity in selected tropical estuaries: implications on polychaete diversity and composition towards predicting ecological health. Oceanologia 64:346–362. https://doi.org/10.1016/j.oceano.2022.01.001

    Article  Google Scholar 

  • Paul GF, Miriam EK, Allen JM, Katja F, Benjamin SC, Marie PA, Robert AB, Michael JN, Warren MZ (2005) The rise of oxygen over the past 205 million years and the evolution of large placental mammals. Science 309:2202–2204. https://doi.org/10.1126/science.1116047

    Article  CAS  Google Scholar 

  • Razouls C, Desreuma N, Kouwenberg J, Bovée F (2022) Biodiversity of marine planktonic copepods (morphology, geographical distribution and biological data). Sorbonne University, CNRS. http://copepodes.obs-banyuls.fr/en

  • Riccardi N, Mariotto L (2000) Seasonal variations in copepod body length: a comparison between different species in the Lagoon of Venice. Aquat Ecol 34:243–252. https://doi.org/10.1023/A:1009971507797

    Article  CAS  Google Scholar 

  • Satpathy KK, Sahu G, Mohanty AK, Prasad MVR, Panigrahy RC (2009) Phytoplankton community structure and its variability during southwest to northeast monsoon transition in the coastal waters of Kalpakkam, East coast of India. Int J Ocean Oceanogr 3:43–74

    Google Scholar 

  • Sivakumar K, Nawaz MA, Saboor A (2021) Population composition of calanoid copepods of the Chennai coast, Tamil Nadu. Ind J Geo-Mar Sci 50:693–700

    Google Scholar 

  • Soloranzo L (1969) Determination of ammonia in natural waters by the phenohypochlorite method. Limnol Oceanogr 14:799–801

    Google Scholar 

  • Song H, Wignall PB, Song H, Dai X, Chu D (2019) Seawater temperature and dissolved oxygen over the past 500 million years. J Earth Sci 30:236–243. https://doi.org/10.1007/s12583-018-1002-2

    Article  CAS  Google Scholar 

  • Sridhar RT, Thangaradjou S, Kumar S, Kannan L (2006) Water quality and phytoplankton characteristics in the Palk Bay, Southeast coast of India. J Environ Biol 27(3):561–566

    CAS  PubMed  Google Scholar 

  • Strickland J, Parsons T (1972) A practical handbook of seawater analysis. Bull Fish Res Board Canada. https://doi.org/10.2307/1979241

    Article  Google Scholar 

  • Sukumaran MK, Muthukumaravel K, Sivakami R, Mohideen K (2013) Seasonal variation in physico-chemical characteristics of Agniar estuary, Southeast coast of India. Asia Pac J Res 2:108–120

    Google Scholar 

  • Tsunashima A, Itoh H, Katano T (2021) Effects of temperature and phytoplankton community composition on subitaneous and resting egg production rates of Acartia omorii in Tokyo Bay. Sci Rep 11:1–19. https://doi.org/10.1038/s41598-021-86976-8

    Article  CAS  Google Scholar 

  • Umer KS, Ebenezer V, Subramoniam T (2020) A short-term study on the effect of environmental factor variation on a zooplankton community. Indian J Geo-Mar Sci 49:1158–1164

    Google Scholar 

  • Utami E, Mahardika G, Anggraeni. Rosalina D (2021) Chlorophyll a concentration of Phytoplankton in Estuary Mangrove Kurau, Bangka Tengah, Indonesia. In: IOP Conference Series: Earth and Environmental Science 926: 012032

  • Vajravelu M, Martin Y, Ayyappan S, Mayakrishnan M (2018) Seasonal influence of physico-chemical parameters on phytoplankton diversity, community structure and abundance at Parangipettai coastal waters, Bay of Bengal, South East Coast of India. Oceanologia 60:114–127. https://doi.org/10.1016/j.oceano.2017.08.003

    Article  Google Scholar 

  • Verberk WC, Atkinson D, Hoefnagel KN, Hirst AG, Horne CR, Siepel H (2021) Shrinking body sizes in response to warming: explanations for the temperature–size rule with special emphasis on the role of oxygen. Biol Rev 96(1):247–268

    Article  PubMed  Google Scholar 

  • Viitasalo M, Koski M, Pellikka K, Johansson S (1995) Seasonal and long-term variations in the body size of planktonic copepods in the northern Baltic Sea. Mar Biol 123:241–250. https://doi.org/10.1007/BF00353615

    Article  Google Scholar 

  • Walczyńska A, Sobczyk Ł (2017) The underestimated role of temperature–oxygen relationship in large-scale studies on size-to-temperature response. Ecol Evol 7:7434–7441. https://doi.org/10.1002/ece3.3263

    Article  PubMed  PubMed Central  Google Scholar 

  • Wood ED, Armstrong FAJ, Richards FA (1967) Determination of nitrate in sea water by cadmium-copper reduction to nitrite. J Mar Biol Assoc UK 47:23–31

    Article  CAS  Google Scholar 

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Acknowledgements

The authors would like to express their sincere thanks to the Management, Principal, and Head of the Department of Biotechnology at Karpaga Vinayaga College of Engineering and Technology in India for supplying the essential resources. The authors would like to thank the Management, Principal, and Head of the Department of Biotechnology at St. Joseph's College of Engineering in India for their assistance throughout the study period.

Funding

This study was funded by Ministry of Earth Sciences (MoES), Government of India (MoES/36/OOIS/Extra/2018).

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MAN designed the research work, executed the research work, collected the zooplankton samples, analyzed the samples, identified the animals up to species level, interpreted the data and drafted the manuscript. KS acquired funding for the research work, collected the samples, analyzed the samples, and helped in species identification. GB analyzed environmental parameters, reviewed and finalized the manuscript. GB and KS supervised the entire work.

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Correspondence to Gurunathan Baskar.

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Nawaz, M.A., Sivakumar, K. & Baskar, G. Seasonal dynamics of body size in calanoid copepods (Calanoida: Copepoda) from the stressed tropical coast of India, Chennai, Bay of Bengal. Aquat Ecol (2023). https://doi.org/10.1007/s10452-023-10075-1

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