Skip to main content
Log in

Hawaiian flying squid Nototodarus hawaiiensis (Cephalopoda: Ommastrephidae) in the Arabian Sea: range extension, age, and growth

  • Original Paper
  • Published:
Marine Biodiversity Aims and scope Submit manuscript

Abstract

The oceanic cephalopod fauna of the Arabian Sea has not been well studied. The Hawaiian flying squid Nototodarus hawaiiensis (Oegopsida: Ommastrephidae) is known to have a very broad, disjunct distribution in tropical to subtropical waters. In the present study, the squid Nototodarus hawaiiensis is reported for the first time from the Arabian Sea. Five females ranging in size from 62 to 128 mm dorsal mantle length (DML) were collected. Age estimates based on the statolith-increment analysis ranged from 79 to 132 days, with growth rates ranging from 0.78 to 0.99 (mean = 0.93) mm DML/day. Back-calculated hatch dates occurred from November to January. Stomach-content analysis revealed that the dominant prey was crustaceans.

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

References

  • Arkhipkin AI (1996) Age and growth of the squid Aabraliopsis pfefferi (Oegpsida: Enoploteuthidae) from the Central-East Atlantic based on statolith microstructure. Sci Mar 60:325–330

    Google Scholar 

  • Arkhipkin AI (1997) Age and growth of the mesopelagic squid Ancistrocheirus lesueurii (Oegopsida: Ancistrocheiridae) from the central-east Atlantic based on statolith microstructure. Mar Biol 129:103–111. https://doi.org/10.1007/s002270050151

  • Arkhipkin AI, Shcherbich ZN (2012) Thirty years’ progress in age determination of squid using statoliths. J Mar Biol Assoc UK 92:1389–1398. https://doi.org/10.1017/S0025315411001585

    Article  Google Scholar 

  • Arkhipkin AI, Rodhouse PGK, Pierce GJ, Sauer W, Sakai M, Allcock L, Arguelles J, Bower JR, Castillo G, Ceriola L, Chen C, Chen X, Diaz-Santana M, Downey N, González AF, Amores JG, Green CP, Guerra A, Hendrickson LC et al (2015) World Squid Fisheries. Rev Fish Sci Aquac 23(2):92–252. https://doi.org/10.1080/23308249.2015.1026226

    Article  Google Scholar 

  • Berry SS (1918) Report on the Cephalopoda Obtained by the F.I.S. "Endeavour" in the Great Australian Bight and Other Southern Australian Localities. Biological Results of the Fishing Experiments carried on by the F.I.S. "Endeavour", 1909-1914 4(5):201–298

  • Braid HE (2018) Taxonomy id destiny: resolving the systematics of unstable squid families using integrative taxonomy to aid cephalopod conservation. PhD Thesis, Auckland University of Technology, New Zealand

  • Braid HE, Bolstad KS (2019) Cephalopod biodiversity of the Kermadec Islands: implications for conservation and some future taxonomic priorities. Invertebr Syst 33(2):402–425. https://doi.org/10.1071/IS18041

  • Chakraborty RD, Nandakumar G, Maheswarudu G, Chellapan K, Sajeev CK, Purushothaman P, Kuberan G (2014) Fishery and biology of Plesionika quasigrandis Chace, 1985 off Sakthikulangara, south-west coast of India. Indian J Fish 61(4):10–17

    Google Scholar 

  • Collins MA, De Grave S, Lordan C, Burnell RPG (1994) Diet of the squid Loligo forbesi Steenstrup (Cephalopoda: Loliginidae) in Irish waters. ICES J Mar Sci 51:337–344

    Article  Google Scholar 

  • Dawe EG, O’dor RK, Odense PH, Hurley GV (1985) Validation and application of an ageing technique for short-finned squid (Illex illecebrosus). J Northwest Atlantic Fish Sci 6:107–116

    Article  Google Scholar 

  • Dong Z (1963) A priliminary taxonomic study of the Cephalopoda from the Chinese waters. Studia Marina Sinica 4:125–162

    Google Scholar 

  • Dunn MR (2009) Feeding habits of the ommastrephid squid Nototodarus sloanii on the Chatham Rise, New Zealand. New Zealand J Mar Fre Res 43:1103–1113. https://doi.org/10.1080/00288330.2009.9626533

    Article  Google Scholar 

  • Dunning M (1988a) First records of Nototodarus hawaiiensis (Berry, 1912) (Cephalopoda: Ommstrephidae) from northern Australia with a reconsideration of the identity of N. sloani philippinensis Voss, 1962. Mem Mus Victoria 49:159–168

    Article  Google Scholar 

  • Dunning M (1988b) Distribution and comparative life history studies of deepwater squid of the family Ommastrephidae in Australasian waters. PhD Thesis, Department of Zoology, University of Queensland, Brisbane, Australia, p-288

  • Dunning MC, Förch EC (1998) A review of the systematics, distribution and biology of arrow squids of the genus Nototodarus Pfeffer, 1912 (Cephalopoda: Ommastrephidae), pp 393-404. In: Voss N, Vecchione M, Toll RB, Sweeney MJ (eds) (1998) Systematics and biogeography of cephalopods. Smithsonian Contrib Zool 586(1):1–276

  • Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome coxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biote l3: 294–299

  • Gebhardt K, Knebelsberger T (2015) Identification of cephalopod species from the North and Baltic Seas using morphology, COI and 18S rDNA sequences. Helgol Mar Res 69:259–271. https://doi.org/10.1007/s10152-015-0434-7

  • Harman RF, Young RE (1985) The larvae of Ommastrephid squids (Cephalopoda: Teuthoidea) from Hawaiian waters. Vie Milieu 35:211–222

    Google Scholar 

  • Hoang DT, Chernomor O, Von Haeseler A, Minh BQ, Vinh LS (2018) UFBoot2: improving the ultrafast bootstrap approximation. Mol Biol Evol 35(2):518–522. https://doi.org/10.1093/molbev/msx281

  • Jackson GD, Wadley VA (1998) Age growth, and reproduction of the tropical squid Nototodarus hawaiiensis (Cepahlopoda: Ommastrephidae) off the North West Slope of Australia. Fish Bull 96:779–787

    Google Scholar 

  • Jackson GD, Forsythe JW, Hixon RF, Hanlon RT (1997) Age, growth, and maturation of Lolliguncula brevis (Cephalopoda: Loliginidae) in the northwest Gulf of Mexico with a comparison of length-frequency versus statolith age analysis. Can J Fish Aquat Sci 54:2907–2919. https://doi.org/10.1139/f97-192

  • Jackson GD, Wotherspoon S, McGrath-Steer BL (2005) Temporal population dynamics in arrow squid Nototodarus gouldi in southern Australian waters. Mar Biol 146(5):975–983. https://doi.org/10.1007/s00227-004-1491-7

  • Kalyaanamoorthy S, Minh BQ, Wong TK, Von Haeseler A, Jermiin LS (2017) ModelFinder: fast model selection for accurate phylogenetic estimates. Nat Methods 14(6):587–589. https://doi.org/10.1038/nmeth.4285

  • Lipinski MR (1979) Universal maturity scale for the commercially-important squids (Cephalopoda: Teuthoidea). The results of maturity classification of the Illex illecebrosus (LeSuer, 1821) populations for the years 1973-1977. Int Comm Northwest Atl Fish ICNAF Res, pp 1–14

  • Mcgregor V, Large K (2015) Progress with in-season modelling of squid within New Zealand’s EEZ and Management strategy evolution (MSE). Documents of South Pacific Regional Fisheries Management Organization 3rd meeting (SC-03-26)

  • Miller SA, Dykes DD, Polesky HFRN (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16(3):12–15

    Article  Google Scholar 

  • Mohamed KS, Sajikumar KK, Ragesh N, Ambrose TV, Jayasankar J, Said Koya KP, Sasikumar G (2018) Relating abundance of purpleback flying squid Sthenoteuthis oualaniensis (Cephalopoda: Ommastrephidae) to environmental parameters using GIS and GAM in south-eastern Arabian Sea. J Nat Hist 52(29):1869–1882. https://doi.org/10.1080/00222933.2018.1497721

    Article  Google Scholar 

  • Nesis (1970) Occurance of a rare squid, Chaunoteuthis mollis Appellof (Family Onychoteuthidae) in the Indian Ocean. Veliger 12(3):290–291

    Google Scholar 

  • Nesis KN (1987) Cephalopods of the world. T.F.H. Publications, Neptune City, NJ

  • Nguyen LT, Schmidt HA, Von Haeseler A, Minh BQ (2015) IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol 32(1):268–274. https://doi.org/10.1093/molbev/msu300

  • Okutani T, Kuroiwa M (1985) The first occurrence of Nototodarus (Cephalopoda: Ommastrephidae) from off Chile, southeast Pacific (preliminary report). Venus 44(2):95–102

    Google Scholar 

  • Piatkowski U, Welsch W (1991) On the distribution of pelagic cephalopods in the Arabian Sea. Bull Mar Sci 49:186–198

    Google Scholar 

  • Rajan KN, Nandakumar GK, Chellappan K (2001) Innovative exploitation of deep-sea crustaceans along the Kerala coast. Mar Fish Infor Serv T & E Ser 168:1–5

    Google Scholar 

  • Roper CFE, Voss GL (1983) Guidelines for taxonomic descriptions of cephalopod species. Memories of National Museum of Victoria 44:49–63

    Google Scholar 

  • Roper CFE, Sweeney MJ, Nauen CE (1984) FAO Species Catalogue. Vol 3. Cephalopod of the World. An annotated and illustrated catalogue of species of interest to fisheries. FAO Fisheries Synopsis, 125(3):277 pp

  • Roper CFE, Nigmatullin C, Jereb P (2010) Family Ommastrephidae. In: Jereb P, Roper CFE (eds) Cephalopods of the world. An annotated and illustrated catalogue of species known to date. Volume 2. Myopsid and Oegopsid Squids. FAO Species Catalogue for Fishery Purposes. No. 4, Vol. 2. Rome, FAO, pp 269–347

  • Sajikumar KK, Arkhipkin AI, Venkatesan V, Jestin Joy KM, Binesh CP, Sasikumar G, Mohamed KS (2017) Range extension of a bathypelagic squid, Bathyteuthis bacidifera (Cephalopoda: Bathyteuthidae), to the south Arabian Sea with special reference to its age and growth pattern. Mar Biodivers 48:1511–1518. https://doi.org/10.1007/s12526-017-0655-x

  • Sajikumar KK, Venkatesan V, Binesh CP, Mohan G, Sanil NK, Kripa V, Mohamed KS (2018) Presence of the Wondrous jewel squid Histioteuthis miranda (Cephalopoda: Histioteuthidae) in the eastern Arabian Sea and determination of its age from statoliths. Thalassas 34:383–390. https://doi.org/10.1007/s41208-018-0076-z

  • Sajikumar KK, Sasikumar G, Venkatesan V, Vidya R, Alloycious PS, Jestin Joy KM, Karamathullah PS, Nataraja GD, Mohamed KS (2020) Distribution, age and growth of the diamondback squid, Thysanoteuthis rhombus (Cephalopoda: Thysanoteuthidae) from the tropical Arabian Sea. Fish Res 224(105478). https://doi.org/10.1016/j.fishres.2019.105478

  • Sato T (1985) Reports on the Squid Tagging in New Zealand Waters. Far Seas Fisheries Research Laboratory, Series, 14:1–73

  • Silva L, Balguerías E, Afonso PS, Sobrino I, Gill J, Burgos C (2009) Cephalopod Species in Mozambican Waters Caught in the “Mozambique 0307” Survey: Distribution, Abundance and Assemblages. West Indian Ocean J Mar Sci 8:37–48

    Google Scholar 

  • Sreeja V, Norman MD, Bijukumar A (2015) A new species of pouched octopus, Cistopus Gray, 1849 (Cephalopoda: Octopodidae) from the southwest coast of India. Zootaxa 4058(2):244–256. https://doi.org/10.11646/zootaxa.4058.2.6

  • Tamura K, Stecher G, Kumar S (2021) MEGA11: molecular evolutionary genetics analysis version 11. Mol Biol Evol 38(7):3022–3027. https://doi.org/10.1093/molbev/msab120

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Uozumi Y (1998) Fishery biology of arrow squids, Nototodarus gouldi and N. sloanii in New Zealand waters. Bulletin of the National Research Institute of Far Seas Fisheries 35: 1–111

  • Uozumi Y, Ohara H (1993) Age and growth of Nototodarus sloanii (Cephalopoda: Oegopsida) based on daily increments counts in statoliths. Nippon Suisan Gakkaishi 59:1469–1477

    Article  Google Scholar 

  • Velasco A, Ramilo-Fernández G, Sotelo CG (2020) A real-time PCR method for the authentication of common cuttlefish (Sepia officinalis) in food products. Foods 9(3):286. https://doi.org/10.3390/foods9030286

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Villanueva R (1992) Interannual growth differences in the oceanic squid Todarodes angolensis Adam in the northern Benguela up-welling system, based on statolith growth increment analysis. J Exp Mar Biol Ecol 159:157–177

    Article  Google Scholar 

  • Wakabayashi T, Suzuki N, Sakai M et al (2006) Identification of ommastrephid squid paralarvae collected in northern Hawaiian waters and phylogenetic implications for the family Ommastrephidae using mtDNA analysis. Fish Sci 72:494–502. https://doi.org/10.1111/j.1444-2906.2006.01177.x

    Article  CAS  Google Scholar 

  • Wakabayashi T, Suzuki N, Sakai M, Ichii T, Chow S (2012) Phylogenetic relationships among the family Ommastrephidae (Mollusca: Cephalopoda) inferred from two mitochondrial DNA gene sequences. Mar Genom 7:11–16. https://doi.org/10.1016/j.margen.2012.04.005

  • Wormuth JH (1976) The biogeography and numerical taxonomy of the Oegopsid squid family Ommastrephidae in the Pacific Ocean. Bulletin of the Scripps Institution of Oceanography 23:1-90

  • Young RE (1978) Vertical distribution and photosensitive vesicles of pelagic cephalopods from Hawaiian waters. Fish Bull 76(3):583–615

    Google Scholar 

  • Zhang J, Kapli P, Pavlidis P, Stamatakis A (2013) A general species delimitation method with applications to phylogenetic placements. Bioinformatics. 29(22):2869–2876. https://doi.org/10.1093/bioinformatics/btt499

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We are thankful to Director of ICAR-CMFRI for facilities and encouragements. We are indebted to Malcolm Dunning, Honorary Research Fellow, Queensland Museum and C M. Nigmatullin, Russia, for help in the identification of the specimen. Many thanks are due to the crew of the commercial fishing vessel for the squid and for information that made this study possible. We would also like to thank anonymous reviewers whose valuable and helpful comments greatly improved the manuscript.

Funding

The work was funded by ICAR-CMFRI, Kochi, India.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kurichithara Kunjumony Sajikumar.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Ethical approval

All necessary permits for sampling and observational field studies have been obtained by the authors from the competent authorities and are mentioned in the acknowledgements, if applicable.

Sampling and field studies

All necessary permits for sampling and observational field studies have been obtained by the authors from the competent authorities and are mentioned in the acknowledgements, if applicable.

Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on request.

Author contribution

KKS and GS conceived and designed research. KKS, PL, VV, RV, PSA, and KMJJ conducted morphological species identification. SV made genetic analyses. PP made the distribution map. All authors contributed to manuscript writing and read and approved the manuscript.

Additional information

Communicated by M. Vecchione

Publisher’s note

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

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sajikumar, K.K., Laxmilatha, P., Vargheese, S. et al. Hawaiian flying squid Nototodarus hawaiiensis (Cephalopoda: Ommastrephidae) in the Arabian Sea: range extension, age, and growth. Mar. Biodivers. 53, 15 (2023). https://doi.org/10.1007/s12526-022-01325-w

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s12526-022-01325-w

Keywords

Navigation