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Comparison of the parasite community of two notothens, Notothenia rossii and N. coriiceps (Pisces: Nototheniidae), from King George Island, Antarctica

Published online by Cambridge University Press:  01 October 2018

G. Muñoz Open the ORCID record for G. Muñoz [Opens in a new window]  and
M. Rebolledo
G. Muñoz*
Affiliation:
Facultad de Ciencias del Mar y de Recursos Naturales, Universidad de Valparaíso, Avenida Borgoño 16344, Viña del Mar, Chile
M. Rebolledo
Affiliation:
Facultad de Ciencias del Mar y de Recursos Naturales, Universidad de Valparaíso, Avenida Borgoño 16344, Viña del Mar, Chile
*
Author for correspondence: G. Muñoz, E-mail: [email protected]
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Abstract

In this study, we analysed and compared the whole parasite community from the fish Notothenia rossii and Notothenia coriiceps collected from Fildes Bay at King George Island, Antarctica, during January–February 2017 in a field campaign supported by the Chilean Antarctic Institute. The fish samples collected were 45 specimens of N. rossii and 22 of N. coriiceps, with total lengths averaging 29.7 ± 5.3 cm and 32.5 ± 3.2 cm, respectively. Fish were dissected to collect their internal and external parasites. All the fish were parasitized; 13 taxa were found in N. rossii and 12 taxa in N. coriiceps. Acanthocephalans, mainly Metacanthocephalus johnstoni and Aspersentis megarhynchus, were the most abundant and prevalent parasites in both fish species. The abundance and richness of the parasite infracommunity increased with the host body length only in N. rossii. Twelve parasitic taxa were shared by both notothen species. Abundance and prevalence of parasitic taxa, as well as the average richness and abundance of the parasite infracommunities were mostly similar between the two fish species. Parasite compositions of N. coriiceps reported in published studies from King George Island were relatively comparable to our sample. We concluded that the two congeneric and sympatric fish species had highly similar parasite communities, which indicates that they use resources in a similar way, thus allowing them to become parasitized with the same parasitic species and in the same abundances. All parasites recorded in this study have been found in several other fish species; therefore, parasites from notothens are considered to be generalists.

Keywords

Antarctic fishNototheniaparasite communitiesparasite diversity
Type
Research Paper
Information
Journal of Helminthology , Volume 93 , Issue 6 , November 2019 , pp. 732 - 737
Copyright
Copyright © Cambridge University Press 2018 

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References

Bush, AO et al. (1997) Parasitology meets ecology on its own terms Margolis et al. revisited. The Journal of Parasitology 83, 575–583.Google Scholar
Cali, F et al. (2017) Life history traits of Notothenia rossii and N. coriiceps along the southern Scotia Arc. Polar Biology 40, 1409–1423.Google Scholar
Casaux, RJ and Barrera-Oro, ER (2002) Effect of a shore-based sampling programme on Notothenia coriiceps populations. Antarctic Science 14, 221–224.Google Scholar
Chao, A et al. (2006) Abundance-based similarity indices and their estimation when there are unseen species in samples. Biometrics 62, 361–371.Google Scholar
Clarke, KR and Warwick, RM (1994) Change in Marine Communities: An Approach to Statistical Analysis and Interpretation. Bournemouth: Natural Environment Research Council.Google Scholar
Cohen, BF and Poore, GC (1994) Phylogeny and biogeography of the Gnathiidae (Crustacea: Isopoda) with descriptions of the new genera and species, most from South-Eastern Australia. Memoirs of the Museum of Victoria 54, 271–379.Google Scholar
Desdevises, Y et al. (2002) Evolution and determinants of host specificity in the genus Lamellodiscus (Monogenea). Biological Journal of the Linnean Society 77, 431–443.Google Scholar
DeWitt, HH, Heemstra, PC and Gon, O (1990) Nototheniidae. In Gon, O and Heemstra, PC (eds), Fishes of the Southern Ocean. Grahamstown: J. L. B. Smith Institute of Ichthyology, pp. 279–331.Google Scholar
Eastman, JT (2005) The nature of the diversity of Antarctic fishes. Polar Biology 28, 93–107.Google Scholar
Esch, GW and Fernandez, JA (1993) A Functional Biology of Parasitism: Ecological and Evolutionary Implications. London: Chapman and Hall.Google Scholar
Froese, R and Pauly, D (2018) FishBase. Available at www.fishbase.org.Google Scholar
Laskowski, Z and Rocka, A (2014) Molecular identification larvae of Onchobothrium antarcticum (Cestoda: Tetraphyllidea) from marbled rockcod, Notothenia rossii in Admiralty Bay (King George Island, Antarctica). Acta Parasitologica 59, 767–772.Google Scholar
Laskowski, Z and Zdzitowiecki, K (2005) The helminth fauna of some notothenioid fishes collected from the shelf of Argentine Islands, West Antarctica. Polish Polar Research 26, 315–324.Google Scholar
Laskowski, Z and Zdzitowiecki, K (2017) Acanthocephalans in Sub-Antarctic and Antarctic. In Klimpel, S, Kuhn, T and Mehlhorn, H (eds),. Biodiversity and Evolution of Parasitic Life in the Southern Ocean, Parasitology Research Monograph, Vol. 9. Cham: Springer, pp. 141–182.Google Scholar
Laskowski, Z, Korczak-Abshire, M and Zdzitowiecki, K (2012) Changes in acanthocephalan infection of the Antarctic fish Notothenia coriiceps in Admiralty Bay, King George Island, over 29 years. Polish Polar Research 33, 99–108.Google Scholar
Laskowski, Z, Jeżewski, W and Zdzitowiecki, K (2014) Changes in digenean infection of the Antarctic fish Notothenia coriiceps in Admiralty Bay, King George Island, over three decades. Polish Polar Research 35, 513–520.Google Scholar
Lutnicka, H and Zdzitowiecki, K (1984) On some problems related to the occurrence of Pseudobenedenia nototheniae Lohnston, 1931 (Monogenea, Capsalidae, Trochopodinae) off the South Shetlands. Acta Ichthyologica et Piscatoria 14, 141–147.Google Scholar
Meyer, MC and Burreson, EM (1990) Some leeches (Hirudinea: Piscicolidae) of the southern oceans. Biology of the Antarctic Seas XXI 52, 219–236.Google Scholar
Moreno, CE (2001) Métodos para medir la biodiversidad. Zaragoza: Manuales y Tesis SEA.Google Scholar
Moteki, M et al. (2011) Spatial distribution of pelagic fish off Adélie and George V Land, East Antarctica in the austral summer 2008. Polar Science 5, 211–224.Google Scholar
Muñoz, G, Grutter, AS and Cribb, TH (2006) Endoparasite communities of five fish species (Labridae: Cheilininae) from Lizard Island: How important is the ecology and phylogeny of the hosts? Parasitology 132, 363–373.Google Scholar
Münster, J et al. (2017) Parasite fauna of the Antarctic dragonfish Parachaenichthys charcoti (Perciformes: Bathydraconidae) and closely related Bathydraconidae from the Antarctic Peninsula, Southern Ocean. Parasites & Vectors 10, 235.Google Scholar
Nezhybová, V and Mašová, S (2015) Basic epidemiological data on metazoan parasites of notothenioid fish off James Ross Island (Prince Gustav Channel, Weddell Sea), Antarctica. Czech Polar Reports 5, 44–54.Google Scholar
Oğuz, MC et al. (2015) Metazoan parasites of Antarctic fishes. Turkiye Parazitoloji Derneğig 39, 174–178.Google Scholar
Palm, HW et al. (1998) The role of the rock cod Notothenia coriiceps (Richardson, 1844) in the life-cycle of Antarctic parasites. Polar Biology 19, 399–406.Google Scholar
Palm, HW, Klimpel, S and Walter, T (2007) Demersal fish parasite fauna around the South Shetland Island: high species richness and low host specificity in deep Antarctic waters. Polar Biology 30, 1513–1522.Google Scholar
Poulin, R (2007) Evolutionary Ecology of Parasites. Princeton, NJ: Princeton University Press.Google Scholar
Rocka, A (2004) Nematodes of the Antarctic fishes. Polish Polar Research 25, 135–152.Google Scholar
Rokiki, J and Zdzitowiecki, K (1991) Dynamics of Eubrachiella antarctica (Quidor, 1906) (Copepoda) occurrence in Notothenia rossii marmorata (Fischer, 1885). Acta Ichthyologica et Piscatoria 21, 45–52.Google Scholar
Sokolov, SG, Khasanov, FK and Gordeev, II (2018) New data on the morphology and phylogenetic connections of Postlepidapedon opisthobifurcatum (Trematoda, Lepocreadioidea: Lepidapedidae), a parasite of Antarctic and sub-Antarctic fishes. Helminthologia 55, 95–101.Google Scholar
Szidat, L (1965) Estudios sobre la fauna de parásitos de peces antárticos. I - Los parásitos de Notothenia neglecta Nybelin. Servicio de Hidrografía Naval, República de Argentina H910, 1–84.Google Scholar
Trontelj, P and Fišer, C (2009) Perspectives: Cryptic species diversity should not be trivialised, Systematics and Biodiversity 7, 1–3.Google Scholar
Utevsky, AY (2005) An identification key to Antarctic fish leeches (Hirudinea: Piscicolidae). Ukrainian Antarctic Journal 3, 135–144.Google Scholar
Utevsky, AY (2007) Antarctic Piscicolid Leeches. Bonn: Zoologisches Forschungsmuseum Alexander Koenig.Google Scholar
Wägele, JW (1987) Description of the postembryonal stages of the Antarctic fish parasite Gnathia calva Vanhöffen (Crustacea: Isopoda) and synonymy with Heterognathia Amar & Roman. Polar Biology 7, 77–92.Google Scholar
Walton, DWH (1987) Antarctic Science. Cambridge: Cambridge University Press.Google Scholar
Zdzitowiecki, K (1990) Antarctic representative of the genus Macvicaria Gibson & Bray, 1982 (Digenea: Opecoelidae), with descriptions of two new species. Systematic Parasitology 16, 169–179.Google Scholar
Zdzitowiecki, K (1997) Antarctic Digenea, Parasites of Fishes. Königstein: Koeltz Scientific Book.Google Scholar
Zdzitowiecki, K and 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
Zdzitowiecki, K and White, MG (1992) Digenean Trematoda infection of inshore fish at South Georgia. Antarctic Science 4, 51–55.Google Scholar
Zdzitowiecki, K and White, MG (1996) Acanthocephalan infection of inshore fish at the South Orkney Islands. Antarctic Science 8, 273–276.Google Scholar
Zdzitowiecki, K and Zadrozny, T (1999) Endoparasitic worms of Harpagifer antarcticus Nybelin, 1947 off the South Shetland Islands (Antarctic). Acta Parasitologica 44, 125–130.Google Scholar