Skip to main content
Log in

Influence of upwelling on the chaetognath community along the Southeastern Arabian Sea

  • Original Paper
  • Published:
Wetlands Ecology and Management Aims and scope Submit manuscript

Abstract

Community structure and distribution of chaetognaths were investigated along the upwelled and non-upwelled waters of Southeastern Arabian Sea (SEAS) from the coastal, shelf and open ocean regions. With the onset of monsoon, intense upwelling along the southern part of SEAS (8° 28′ N) and a weak coastal upwelling along the northern counterpart (15° 30′ N) was evident. Zooplankton biomass was observed to be high in the upwelled waters with the dominance of copepods. Chaetognaths were also observed in significant numbers all along the SEAS, however maximum numerical abundance was observed in the southern upwelled waters. Chaetognaths belonging to 10 genera were identified of which genus Flaccisagitta (54%) made the most dominant group along the entire study area followed, in order of abundance, by Serratosagitta (20%), Mesosagitta (18.2%), Sagitta (12.3%), Ferosagitta (11%) and Krohnitta (6.4%). Flaccisagitta were observed to be abundant in the upwelled waters along with Pterosagitta, Serratosagitta, Sagitta, Krohnitta and Ferosagitta whereas genus Mesosagitta dominated the non-upwelled waters of northern transects.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

Data availability

The manuscript has no associated data.

References

  • Alvarino A (1964) The chaetognatha of the monsoon expedition in the Indian Ocean. Pac Sci 28:336–348

    Google Scholar 

  • Aravindakshan PN, Sakthivel M (1973) The location of cephalopod nurseries in the Indian Ocean. In Handbook to the international zooplankton collections, vol V. National Institute of Oceanography, Cochin, pp 70–75

  • Ashjian CJ, Smith SL, Flagg CN, Idrisi N (2002) Distribution, annual cycle, and vertical migration of acoustically derived biomass in the Arabian Sea during 1994–1995. Deep-Sea Res II 49:2377–2402. https://doi.org/10.1016/S0967-0645(02)00041-3

    Article  Google Scholar 

  • Atkinson A (1996) Subantarctic copepods in an oceanic, low chlorophyll environment: ciliate predation, low food selectivity and impact on prey populations. Mar Ecol Prog Ser 130:85–96

    Article  Google Scholar 

  • Azam F, Fenchel T, Field JG, Grey JS, Meyer-Reil LA, Thingstad F (1983) The ecological role of water-column microbes. Mar Ecol Prog Ser 10:257–263

    Article  Google Scholar 

  • Banse K, English DC (2000) Geographical differences in seasonality of CZCS-derived phytoplankton pigment in the Arabian Sea for 1978–1986. Deep-Sea Res Part II 47(7–8):1623–1677. https://doi.org/10.1016/S0967-0645(99)00157-5

    Article  Google Scholar 

  • Bhattathiri PMA, Pant A, Sawant S, Gauns M, Matondkar SGP, Mohanraju R (1996) Phytoplankton production and chlorophyll distribution in the eastern and central Arabian Sea. Curr Sci 71(11):857–862

    Google Scholar 

  • Bieri R (1959) The distribution of the planktonic Chaetognatha in the Pacific and their relationship to the water masses. Limnol Oceanogr 4(1):1–28. https://doi.org/10.4319/lo.1959.4.1.0001

    Article  Google Scholar 

  • Bieri R (1991) Systematics of the chaetognatha. In: Bone Q, Kapp H, Pierrot-Bults AC (eds) The biology of chaetognaths. Oxford University Press, Oxford, pp 122–136

    Google Scholar 

  • Brinton E, Gopalakrishnan K (1973) The distribution of Indian Ocean euphausiids. In: Zeitzschel B, Gerlach SA (eds) The biology of the Indian Ocean. Springer-Verlag, Berlin, pp 357–382

    Chapter  Google Scholar 

  • Brock J, McClain C, Luther M, Hay W (1991) The phytoplankton bloom in the northwestern Arabian Sea during the southwest monsoon of 1979. J Geophys Res 96:20623–20642. https://doi.org/10.1029/91JC01711

    Article  Google Scholar 

  • Casanova JP, Nair VR (1999) A new species of the genus Sagitta (phylum Chaetognatha) from the Agatti lagoon (Laccadive Archipelago, Indian Ocean) with comments on endemism. Ind J Mar Sci 28(2):169–172

    Google Scholar 

  • Chacko PI (1950) Marine plankton from waters around the Krusadai Island. Proc Indian Acad Sci Sect B 31(3):162–174

    Article  Google Scholar 

  • Cheney J (1985) Spatial and temporal abundance patterns of oceanic chaetognaths in the western North Atlantic—II Vertical distributions and migrations. Deep Sea Res Part A 32(9):1061–1075. https://doi.org/10.1016/0198-0149(85)90062-7

    Article  Google Scholar 

  • Feigenbaum DL, Maris RC (1984) Feeding in the Chaetognatha. Oceanogr Mar Biol Annu Rev 22:343–392

    Google Scholar 

  • Ganapati PN, Rao TSS (1954) Studies on the Chaetognatha off the Visakhapatnam coast, Part I. Seasonal fluctuations in relation to salinity and temperature. Andhra Univ Mem Oceanogr (Ser 49) 1:143–150

    Google Scholar 

  • George PC (1952) A systematic account of the chaetognatha of the Indian coastal waters, with observations on their seasonal fluctuations along the Malabar Coast. Proc Natl Inst Sci India 18(6):657–689

    Google Scholar 

  • George J (1969) A preliminary report on the distribution and abundance of planktonic ostracods in the Indian Ocean. In Proceedings of the symposium on Indian Ocean. National Institute of Sciences of India, New Delhi, pp 641–647

  • Gibbons MJ (1992) Diel feeding and vertical migration of Sagitta serratodentata Krohntasmanica Thomson (Chaetognatha) in the southern Benguela. J Plankton Res 14(2):249–259. https://doi.org/10.1093/plankt/14.2.249

    Article  Google Scholar 

  • Giesecke R, González HE (2004) Feeding of Sagitta enflata and vertical distribution of chaetognaths in relation to low oxygen concentrations. J Plankton Res 26(4):475–486. https://doi.org/10.1093/plankt/fbh039

    Article  Google Scholar 

  • Gopalakrishnan K, Brinton E (1969) Preliminary observations on the distribution of Euphausiacea from the International Indian Ocean Expedition. In Proceedings of the symposium on Indian Ocean. National Institute of Sciences of India, New Delhi, pp 594–611

  • Goswami SC, Sarupria JS, Bhargava RMS (1992) Zooplankton standing stock assessment and fishery resources in the Indian Seas. In: Desai BN (ed) Oceanography of the Indian Ocean. Oxford & IBH Published Company, New Delhi, pp 217–226

    Google Scholar 

  • Grasshoff K, Ehrhardt M, Kremling K, Almgren T (1983) Methods of seawater analysis. Verlag Chemie, Weinheim, p 419

    Google Scholar 

  • Gray P (1961) Encyclopedia of biological science. Reinhold Publishing Corp, New York

    Google Scholar 

  • Gurumurthy GP, Tripti M, Riotte J, Prakyath R, Balakrishna K (2017) Impact of water-particle interactions on molybdenum budget in humid tropical rivers and estuaries: insights from Nethravati, Gurupur and Mandovi river systems. Chem Geol 450:44–58. https://doi.org/10.1016/j.chemgeo.2016.12.008

    Article  CAS  Google Scholar 

  • Harris R, Lenz J, Skjoldal HR, Huntley M (2000) ICES zooplankton methodology manual. Academic, San Diego

    Google Scholar 

  • John CC (1933) Sagitta of the Madras coast. Government Press, Superintendent, pp 1–10

    Google Scholar 

  • John CC (1937) Seasonal variations in the distribution of Sagitta of the Madras coast. Rec Indian Mus 39(1):83–97

    Google Scholar 

  • Kasturirangan LR, Saraswathy M, Gopalakrishnan TC (1973) Distribution of copepoda in the Indian Ocean. In: Zeitzschel B, Gerlach SA (eds) Biology of the Indian Ocean. Springer Verlag, Berlin, pp 331–333

    Chapter  Google Scholar 

  • Krey J, Babenerd B (1976) Phytoplankton production: atlas of the international Indian Ocean expedition. Institutfür Meereskundean der Universität Kiel.

  • Kumari LK, Achuthanktty CT (1989) Standing stock and biogeochemical composition of zooplankton in the northeastern Arabian Sea. Indian Journal of Marine Science 18:103–105

    Google Scholar 

  • Kusum KK (2012) Ecology of Chaetognaths in the Indian EEZ. Ph.D Thesis, Cochin University of Science and Technology.

  • Kusum KK, Vineetha G, Raveendran TV, Muraleedharan KR, Biju A, Achuthankutty CT (2014) Influence of upwelling on the distribution of chaetognath (zooplankton) in the oxygen deficient zone of the eastern Arabian Sea. Cont Shelf Res 78:16–28. https://doi.org/10.1016/j.csr.2014.01.005

    Article  Google Scholar 

  • Lee C, Jones B, Brink K, Fischer A (2000) The upper ocean response to monsoonal forcing in the Arabian Sea: seasonal and spatial variability. Deep-Sea Res II 47:1177–1226. https://doi.org/10.1016/S0967-0645(99)00141-1

    Article  Google Scholar 

  • Madhupratap M, Nair SS, Haridas P, Padmavati G (1990) Response of zooplankton to physical changes in the environment: coastal upwelling along the central west coast of India. J Coast Res 6:413–426

    Google Scholar 

  • Madhupratap M, Kumar SP, Bhattathiri PMA, Kumar MD, Raghukumar S, Nair KKC, Ramaiah N (1996) Mechanism of the biological response to winter cooling in the northeastern Arabian Sea. Nature 384(6609):549. https://doi.org/10.1038/384549a0

    Article  CAS  Google Scholar 

  • Madhupratap M, Nair KNV, Venugopal P, Gauns M, Haridas P, Gopalakrishnan TC, Nair KKC (2004) Arabian Sea oceanography and fisheries. In: Somvanshi VS (ed) Large marine ecosystems: exploration and exploitation for sustainable development and conservation on fish stocks. Fishery Survey of India, pp 482–491

  • McCreary JP, Kohler KE, Hood RR, Olson DB (1996) A four component ecosystem model of biological activity in the Arabian Sea. Prog Oceanogr 37:193–240. https://doi.org/10.1016/S0079-6611(96)00005-5

    Article  Google Scholar 

  • Nair VR (1969) A preliminary report on the biomass of chaetognaths in the Indian Ocean comparing the south-west and north-east monsoon periods. In Proceedings of the symposium on Indian Ocean. National Institute of Sciences of India, New Delhi, pp 747–752.

  • Nair VR, Rao TSS (1973) Chaetognaths of the Arabian Sea. The biology of the Indian Ocean. Springer, Berlin, Heidelberg, pp 293–317

    Chapter  Google Scholar 

  • Nair KKC, Jacob PG, Kumaran S (1973) Distribution and abundance of planktonic amphipods in the Indian Ocean. In: Zeitzschel B, Gerlach SA (eds) The biology of the Indian Ocean. Springer-Verlag, Berlin, pp 349–356

    Chapter  Google Scholar 

  • Nair VR, Peter G, Paulinose VT (1978) Zooplankton studies in the Indian Ocean II. From the Arabian Sea during post monsoon period. Mahasagar 11:35–43

    Google Scholar 

  • Nair VR, Mustafa S, Metha P, Govindan K, Ram MJ, Gajbhiye SN (1998) Biological characteristics of the Vashishti estuary, Maharashtra. 1ndian. J. Mar. Sci. 27:310–316

    CAS  Google Scholar 

  • Nair VR, Terazaki M, Jayalakshmy KV (2002) Abundance and community structure of chaetognaths in the northern Indian Ocean. Plankton Biology and Ecology 49(1):27–37

    Google Scholar 

  • Nair VR, Kusum GKKR, Nair M (2015) The distribution of the chaetognath population and its interaction with environmental characteristics in the Bay of Bengal and the Arabian Sea. Marine Biology Research 11(3):269–282. https://doi.org/10.1080/17451000.2014.914224

    Article  Google Scholar 

  • Panikkar NK (1969) Fishery resources of the Indian Ocean. In Proceedings of the symposium on Indian Ocean, National Institute of Sciences of India, New Delhi, pp811–832

  • Panikkar NK (1970) Distribution of Copepoda and decapod larvae in the Indian Ocean. International Indian Ocean Plankton Atlas, Volume II, Fascicle 1. Indian Ocean Biological Center, Kochi, pp 15

  • Panikkar NK, Rao TSS (1973) Zooplankton investigation in Indian waters and the role of the Indian Ocean Biological Centre. In Handbook to the international zooplankton collections, vol V. National Institute of Oceanography 5, Kochi, pp111–162

  • Parsons TR, Maita Y, Lalli CM (1984) A manual of chemical and biological methods for seawater analysis. Pergamon Press, New York

    Google Scholar 

  • Pearre S Jr (1982) Feeding by Chaetognatha: aspects of inter-and intra-specific predation. Mar Ecol Prog Ser 7(1):33–45

    Google Scholar 

  • Peter G (1969a) A preliminary report on the general distribution and variation in abundance of the planktonic polychaetes in the Indian Ocean. In Proceedings of the symposium on Indian Ocean. National Institute of Sciences of India, New Delhi, pp 718–726

  • Peter KJ (1969b) Preliminary report on the density of fish eggs and larvae of the Indian Ocean. In Proceedings of the symposium Indian Ocean. National Institute of Sciences of India, New Delhi, pp 854–863

  • Pitchaikani SJ, Lipton AP (2015) Seasonal variation of zooplankton and pelagic fish catch in the fishing grounds off Tiruchendur coast, Gulf of Mannar. India Ecohydrol Hydrobiol 15(2):89–100. https://doi.org/10.1016/j.ecohyd.2015.04.003

    Article  Google Scholar 

  • Prasannakumar S, Prasad TG (1996) Winter cooling in the northern Arabian Sea. Curr Sci 71:834–841

    Google Scholar 

  • Prasannakumar S, Madhuprathap M, Dileepkumar M, Muraleedharan PM, de Souza SN, Gauns M, Sarma VVSS (2001) High biological productivity in the central Arabian Sea during summer monsoon driven by Ekman pumping and lateral advection. Curr Sci 81:1633–1638

    Google Scholar 

  • Qasim SZ (1982) Oceanography of the northern Arabian Sea. Deep-Sea Res 29:1041–1068

    Article  CAS  Google Scholar 

  • Rao TSS (1958a) Studies on chaetognatha in the Indian seas Part II-the chaetognatha of the Lawson’s Bay, Waltair. Andhra Univ Memo Oceanogr 3:137–146

    Google Scholar 

  • Rao TSS (1958b) Studies on chaetognatha in the Indian seas Part IV-distribution in relation to currents. Andhra Univer Mem Oceanogr 2:164–167

    Google Scholar 

  • Rao TSS, Ganapati PN (1958) Studies on Chaetognatha in the Indian seas Part III. Andhra Univ Mem Oceanogr 2:147–163

    Google Scholar 

  • Reeve MR (1971) Deadly arrow-worm. Sea. Frontiers 17:175–183

    Google Scholar 

  • Russell F (1935) On the value of certain plankton animals as indicators of water movements in the English Channel and North Sea. J Marine Biol Assoc UK 20(2):309–332. https://doi.org/10.1017/S0025315400045239

    Article  Google Scholar 

  • Russell F (1939) Hydrographical and biological conditions in the North Sea as indicated by plankton organisms. ICES J Mar Sci 14(2):171–192. https://doi.org/10.1093/icesjms/14.2.171

    Article  Google Scholar 

  • Ryther JH, Hall JR, Pease AK, Bakun A, Jones MM (1966) Primary organic production in relation to the chemistry and hydrography of the western Indian Ocean. Limnol Oceanogr 11(3):371–380. https://doi.org/10.4319/lo.1966.11.3.0371

    Article  CAS  Google Scholar 

  • ShannonLV, Pillar SC (1986) The Benguela ecosystem Part III-Plankton. In: Barnes M (ed) Oceanogr Mar Biol Annu Rev 24. Aberdeen University Press, pp 65–170.

  • Smith S, Roman M, Prusova I, Wishner K, Gowing M, Codispoti LA, Flagg C (1998) Seasonal response of zooplankton to monsoonal reversals in the Arabian Sea. Deep-Sea Res Part II 45(10–11):2369–2403. https://doi.org/10.1016/S0967-0645(98)00075-7

    Article  Google Scholar 

  • Smitha BR, Sanjeevan VN, Vimalkumar KG, Revichandran C (2008) On the upwelling off the southern tip and along the west coast of India. J Coastal Res 24(sp3):95–102. https://doi.org/10.2112/06-0779.1

    Article  Google Scholar 

  • Terazaki M (1989) Distribution of chaetognaths in the Australian sector of the Southern Ocean during the BIOMASS SIBEX cruise (KH-83—4). Proc NIPR Symp Polar Biol 2:51–60

    Google Scholar 

  • Tokioka T (1965) The taxonomical outline of chaetognatha. Public Seto Marine Biol Lab 12:335–357

    Article  Google Scholar 

  • Ulloa R, Palma S, Silva N (2004) Relationship between spatial distribution of chaetognaths and oceanographic conditions off Concepción Bay, Chile. Deep Sea Res Part II 51(6–9):537–550. https://doi.org/10.1016/j.dsr2.2004.05.002

    Article  Google Scholar 

  • Varadarajan S, Chacko PI (1943) On the arrow worms of Krusadai. Proc Nat Inst Sci India 9:245–248

    Google Scholar 

  • Vega-Pérez LA, Schinke KP (2011) Checklist of chaetognatha phyllum from São Paulo State, Brazil. Biota Neotrop 11:541–550. https://doi.org/10.1590/S1676-06032011000500021

    Article  Google Scholar 

  • Wishner KF, Gowing M, Gelfman MC (1998) Mesozooplankton biomass in the upper l000m in the Arabian Sea: overall seasonal and geographical patterns and relationship gradients. Deep Sea Res II 45:2405–2432. https://doi.org/10.1016/S0967-0645(98)00078-2

    Article  CAS  Google Scholar 

  • Young DK, Kindle J (1994) Physical processes affecting availability of dissolved silicate for diatom production in the Arabian Sea. J Geophys Res 99:22619–22632. https://doi.org/10.1029/94JC01449

    Article  Google Scholar 

  • Zhang JZ, Fischer CJ (2006) A simplified resorcinol method for direct spectrophotometric determination of nitrate in seawater. Mar Chem 99(1–4):220–226. https://doi.org/10.1016/j.marchem.2005.09.008

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors are thankful to the Centre for Marine Living Resources and Ecology, Ministry of Earth Science, for providing the facilities to conduct the research. We also thank crew members of FORV Sagar Sampada for the help rendered during the cruise period.

Author information

Authors and Affiliations

Authors

Contributions

AP wrote the manuscript with input from LCT. AP conducted the field study. AP and LCT contributed to the taxonomic identifications. SBN and KBP supervised this study and provided research materials. All authors read and approved the manuscript.

Corresponding author

Correspondence to K. B. Padmakumar.

Ethics declarations

Conflict of interest

The authors have no conflicts of interest.

Ethical approval

No animal testing was performed during this study.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Purushothaman, A., Thomas, L.C., Nandan, S.B. et al. Influence of upwelling on the chaetognath community along the Southeastern Arabian Sea. Wetlands Ecol Manage 29, 731–743 (2021). https://doi.org/10.1007/s11273-020-09773-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11273-020-09773-6

Keywords

Navigation