Skip to main content

Advertisement

Log in

Helminths of the Antarctic dragonfish, Parachaenichthys charcoti (Perciformes, Notothenioidei, Bathydraconidae) Studied near Galindez Island (Argentine Islands, West Antarctica)

  • Original Paper
  • Published:
Acta Parasitologica Aims and scope Submit manuscript

Abstract

Purpose

The Antarctic dragonfish, Parachaenichthys charcoti is a notothenioid teleost fish endemic to the Southern Ocean surrounding Antarctica. It is a relatively rare fish species; therefore, published data on the parasite communities of P. charcoti are limited. The present study was performed on the Ukrainian Antarctic Station "Akademik Vernadsky", Argentine Islands, West Antarctica and the purpose was to examine the species diversity of the parasites of P. charcoti and to identify the parameters of helminth infection and helminth component community.

Methods

Fifteen specimens of P. charcoti were caught at a depth of 10–30 m and examined using standard parasitological techniques. All helminths (6251 specimens) were collected manually, fixed in 70% ethanol and identified based on their morphology.

Results

All examined specimens of P. charcoti were found to be infected with helminths; each fish harboured 10–20 helminth species (mean 13.2; median 13) and 237–804 helminth specimens (mean 417; median 401). Twenty-seven helminth species were found, including nine species of trematodes, 4 of cestodes, 4 of nematodes and 10 of acanthocephalans. P. charcoti is the definitive host for 11 out of 27 helminth species recorded. In the helminth component community, the diversity indices were 2.03 (Shannon's index) and 0.79 (Simpson's index); Pielou evenness index was 0.61, and Berger–Parker dominance index was 0.38.

Conclusions

Our results indicate a high species diversity and complex structure of the helminth community in Antarctic dragonfish P. charcoti in the Argentine Islands.

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

Similar content being viewed by others

References

  1. Nybelin O (1951) Subantarctic and Antarctic Fishes. Scientific results of the ‘‘Brategg’’ expedition 1947–1948, vol 2. Publication Christensen Hvalfanstmuseum, p 1–32

  2. Casaux RJ, Mazzotta AS, Barrera-Oro ER (1990) Seasonal aspects of the biology and diet of nearshore nototheniid fish at Potter Cove, South Shetland Islands. Antarctica Polar Biol 11(1):63–72. https://doi.org/10.1007/BF00236523

    Article  Google Scholar 

  3. Casaux R, Barrera-Oro E, Baroni A, Ramon A (2003) Ecology of inshore notothenioid fish from the Danco Coast, Antarctic Peninsula. Polar Biol 26:157–165. https://doi.org/10.1007/s00300-002-0463-y

    Article  Google Scholar 

  4. Manilo LG (2006) Ichthyofauna and morphobiological characteristics of mass fish species of coastal waters of Argentine Islands (Antarctica). Zbirnyk prats Zoologichnogo Muzeju 38:5–22 ([In Ukrainian])

    Google Scholar 

  5. Novillo M, Moreira E, Macchi G, Barrera-Oro E (2018) Reproductive biology in the Antarctic bathydraconid dragonfish Parachaenichthys charcoti. Polar Biol 41:2239–2248. https://doi.org/10.1007/s00300-018-2359-5

    Article  Google Scholar 

  6. Veselskyy MV, Khoetskyy PB (2018) Ichthyofauna of the waters of the archipelago of the Argentine Islands (Ukrainian Antarctic expedition 2015–2016). Nauk Zap Ternop Nats Ped Un-ty. Ser Biol 1(72):36–43

    Google Scholar 

  7. Kompowski A, Rojas C (1994) On some biological characters of Parachaenichthys georgianus (Fischer, 1885) (Pisces, Notothenioidei, Bathydraconidae) from the shelf waters of South Georgia (Antarctica). Acta Ichthyol Piscat 24(2):61–75. https://doi.org/10.3750/AIP1994.24.2.08

    Article  Google Scholar 

  8. Barrera-Oro E (2002) The role of fish in the Antarctic marine food web: differences between inshore and offshore waters in the southern Scotia Arc and west Antarctic Peninsula. Antarct Sci 14(4):293–309. https://doi.org/10.1017/S0954102002000111

    Article  Google Scholar 

  9. Ahn DH, Shin SC, Kim BM, Kang S, Kim JH, Ahn I, Park J, Park H (2017) Draft genome of the Antarctic dragonfish, Parachaenichthys charcoti. Gigascience 6(8):1–6. https://doi.org/10.1093/gigascience/gix060

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Daniels RA (1982) Feeding ecology of some fishes of the Antarctic Peninsula. Fish Bull US 80:575–588

    Google Scholar 

  11. Kompowski A (1992) Food and feeding behaviour of Parachaenichthys georgianus (Fischer, 1885) and Parachaenichthys charcoti (Vaillant, 1906) (Pisces, Bathydraconidae). Acta Ichthyol Piscat 22(1):15–29. https://doi.org/10.3750/AIP1992.22.1.02

    Article  Google Scholar 

  12. Takahashi M, Iwami T (1997) The summer diet of demersal fish at the South Shetland Islands. Antarctic Sci 9:407–413. https://doi.org/10.1017/S0954102097000527

    Article  Google Scholar 

  13. Reid K, Arnould JPY (1996) The diet of Antarctic fur seals Arctocephalus gazella during the breeding season at South Georgia. Polar Biol 16:105–114. https://doi.org/10.1007/BF02390431

    Article  Google Scholar 

  14. Xavier JC, Trathan PN, Ceia FR, Tarling GA, Adlard S, Fox D et al (2017) Sexual and individual foraging segregation in Gentoo penguins Pygoscelis papua from the Southern Ocean during an abnormal winter. PLoS ONE 12(3):e0174850. https://doi.org/10.1371/journal.pone.0174850

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Near TJ (2009) Notothenioid fishes (Notothenioidei). In: Hedges SB, Kumar S (eds) The time tree of life. Oxford University Press, pp 339–343

    Google Scholar 

  16. Szidat L, Graefe G (1967) Estudios sobre la fauna de parasitos de peces antarticos II-Los parasitos de Parachaenichthys charcoti. Servicio de Hidrografia Naval, Armada Argentina,República Argentina, Público H, 911, Buenos Aires, pp 1–27

  17. Zdzitowiecki K (2001) Occurrence of endoparasitic worms in fish, Parachaenichthys charcoti (Bathydraconidae), off the South Shetland Islands (Antarctica). Acta Parasitol 46(1):18–23

    Google Scholar 

  18. Zdzitowiecki K (1983) Antarctic acanthocephalans of the genus Metacanthocephalus. Acta Parasitol Pol 28:417–437

    Google Scholar 

  19. Zdzitowiecki K (1986) Prevalence of acanthocephalans in fishes of South Shetland Islands (Antarctic) I. Juvenile Corynosoma spp. Acta Parasitol Pol 30:143–171

    Google Scholar 

  20. Zdzitowiecki K (1986) Prevalence of acanthocephalans in fishes of South Shetland Islands (Antarctic) III Metacanthocephalus johnstoni Zdzitowiecki, 1983, M. dalmori Zdzitowiecki, 1983 and notes on other species; general conclusions. Acta Parasitol Pol 31:125–141

    Google Scholar 

  21. Zdzitowiecki K (1988) Occurrence of digenetic trematodes in fishes off South Shetlands (Antarctic). Acta Parasitol Pol 33:155–167

    Google Scholar 

  22. Zdzitowiecki K (1990) Little known and new Antarctic digenean species of the genera Neolepidapedon and Lepidapedon (Lepocreadiidae). Acta Parasitol Pol 35:19–30

    Google Scholar 

  23. Zdzitowiecki K (1991) Occurrence of digeneans in open sea fishes off the South Shetland Islands and South Georgia, and the list of fish digeneans in the Antarctic. Pol Polar Res 12:55–72

    Google Scholar 

  24. Palm HW (1999) Ecology of Pseudoterranova decipiens (Krabbe, 1878) (Nematoda: Anisakidae) from Antarctic Waters. Parasitol Res 85:638–646. https://doi.org/10.1007/s004360050608

    Article  CAS  PubMed  Google Scholar 

  25. Rocka A (2006) Helminths of Antarctic fishes: Life cycle biology, specificity and geographical distribution. Acta Parasitol 51:26–35. https://doi.org/10.2478/s11686-006-0003-y

    Article  Google Scholar 

  26. Faltýnková A, Georgieva S, Kostadinova A, Bray RA (2017) Biodiversity and Evolution of Digeneans of Fishes in the Southern Ocean. In: Klimpel S, Kuhn T, Mehlhorn H (eds) Biodiversity and evolution of parasitic life in the southern ocean. Parasitology Research Monographs, vol 9. Springer, Charm, pp 49–75. https://doi.org/10.1007/978-3-319-46343-8_5

    Chapter  Google Scholar 

  27. Laskowski Z, Zdzitowiecki K (2017) Acanthocephalans in Sub-Antarctic and Antarctic. In: Klimpel S, Kuhn T, Mehlhorn H (eds) Biodiversity and evolution of parasitic life in the southern ocean. Parasitology Research Monographs, vol 9. Springer, Charm. https://doi.org/10.1007/978-3-319-46343-8_8

    Chapter  Google Scholar 

  28. Wojciechowska A (1993) The tetraphyllidean and tetrabothriid cercoids from Antarctic bony fishes. I. Morphology. Identification with adult forms. Acta Parasitol 38:15–22

    Google Scholar 

  29. Rocka A (1999) Biometrical variability and occurrence of Ascarophis nototheniae (Nematoda, Cystidicolidae), a parasitic nematode of Antarctic and subantarctic fishes. Acta Parasitol 44:188–192

    Google Scholar 

  30. Palm HW, Klimpe S, Walter T (2007) Demersal fish parasite fauna around the South Shetland Islands; high species richness and low host specificity in deep Antarctic waters. Polar Biol 30:1513–1522. https://doi.org/10.1007/s00300-007-0312-0

    Article  Google Scholar 

  31. Münster J, Kochmann J, Grigat J, Klimpel S, Kuhn T (2017) Parasite fauna of the Antarctic dragonfish Parachaenichthys charcoti (Perciformes: Bathydraconidae) and closely related Bathydraconidae from the Antarctic Peninsula. Southern Ocean. Parasit Vector 10:235. https://doi.org/10.1186/s13071-017-2176-7

    Article  Google Scholar 

  32. Zdzitowiecki K, Laskowski Z (2004) Helminths of an Antarctic fish, Notothenia coriiceps, from the Vernadsky Station (Western Antarctica) in comparison with Admiralty Bay (South Shetland Islands). Helminthologia 41:201–207

    Google Scholar 

  33. Weber EP 3rd, Govett P (2009) Parasitology and necropsy of fish. Comp Contin Educ Vet 31(2):E12

    Google Scholar 

  34. Mozgovoy AA (1951) Ascaridata of animals and man, and the diseases caused by them. Osnovy nematodologii, vol 2. Izd-vo AN SSSR, Moskva, pp 1–616 (in Russian)

  35. Zdzitowiecki K, Cielecka D (1997a) Digenea of fishes of the Weddell Sea. II. The genus Macvicaria (Opecoelidae). Acta Parasitol 42:77–83

    Google Scholar 

  36. Zdzitowiecki K, Cielecka D (1997) Digenea of fishes of the Weddell Sea. III. The Lepocreadiidae (genera Neolepidapedon and Lepidapedon), parasites of Notothenioidea. Acta Parasitol 42(2):84–91

    Google Scholar 

  37. Gibson DI, Jones A, Bray RA (2002) Keys to the Trematoda, vol 1. CABI & Natural History Museum, Wallingford, p 544

    Book  Google Scholar 

  38. Jones A, Bray RA, Gibson DI (2005) Keys to the Trematoda, vol 2. CABI & Natural History Museum, Wallingford, p 768. https://doi.org/10.1079/9780851995878.0545

    Book  Google Scholar 

  39. Zdzitowiecki K (1984) Some Antarctic acanthocephalans of the genus Corynosoma parasitizing Pinnipedia, with descriptions of three new species. Acta Parasitol Pol 29:359–377

    Google Scholar 

  40. Zdzitowiecki K (1984) Redescription of Corynosoma hamanni (Linstow, 1892) and description of C. pseudohamanni sp. n. (Acanthocephala) from the environs of the South Shetlands (Antarctic). Acta Parasitol Pol 29:379–393

    Google Scholar 

  41. Zdzitowiecki K (1987) Acanthocephalans of marine fishes in the regions of South Georgia and South Orkneys (Antarctic). Acta Parasitol Pol 31:211–217

    Google Scholar 

  42. Zdzitowiecki K (1996) Acanthocephala in fish in the Weddell Sea (Antarctica). Acta Parasitol 41:199–203

    Google Scholar 

  43. Bush AO, Lafferty KD, Lotz JM, Shostak AW (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. J Parasitol 83(4):575–583. https://doi.org/10.2307/3284227

    Article  CAS  PubMed  Google Scholar 

  44. Rósza L, Reiczigel J, Majoros G (2000) Quantifying parasites in samples of hosts. J Parasitol 86(2):228–232. https://doi.org/10.1645/0022-3395(2000)086[0228:QPISOH]2.0.CO;2

    Article  Google Scholar 

  45. Clarke KR, Gorley RN (2006) PRIMER v6: User Manual/Tutorial (Plymouth Routines in Multivariate Ecological Research). PRIMER-E, Plymouth.

  46. Amin OM (2013) Classification of the acanthocephala. Folia Parasitol 60(4):273–305. https://doi.org/10.14411/fp.2013.031

    Article  Google Scholar 

  47. Kuzmina TA, Salganskij OO, Lisitsyna OI, Korol EM (2020) Helminths of Antarctic rockcod Notothenia coriiceps (Perciformes, Nototheniidae) from the Akademik Vernadsky Station area (Argentine Islands, West Antarctica): new data on the parasite community. Zoodiversity 54(2):99–110. https://doi.org/10.15407/zoo2020.02.099

    Article  Google Scholar 

  48. Linse K, Griffiths HJ, Barnes DKA, Clarke A (2006) Biodiversity and biogeography of Antarctic and sub-Antarctic mollusca. Deep-Sea Res II:985–1008. https://doi.org/10.1016/j.dsr2.2006.05.003

    Article  Google Scholar 

Download references

Acknowledgements

The authors thank Prof. Terry R. Spraker from the Colorado State University for his valuable comments and corrections to the manuscript. This study was partially supported by the National Research Foundation of Ukraine (Project Number 2020.02/0074) and by the National Antarctic Scientific Center, Ministry of Education and Science of Ukraine (Project Number H/12-2020).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tetiana A. Kuzmina.

Ethics declarations

Conflicts of interest/Competing interests

The authors declare that they have no conflict of interest.

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

Kuzmina, T.A., Salganskij, O.O., Dykyy, I.V. et al. Helminths of the Antarctic dragonfish, Parachaenichthys charcoti (Perciformes, Notothenioidei, Bathydraconidae) Studied near Galindez Island (Argentine Islands, West Antarctica). Acta Parasit. 66, 1424–1430 (2021). https://doi.org/10.1007/s11686-021-00417-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11686-021-00417-0

Keywords

Navigation