Abstract
The success of introduced species is often facilitated by escape from the effects of natural predators and parasites. Introduced species can profit from this favourable situation, attaining higher population densities and greater individual sizes in novel areas. In this study, somatic condition and parasite infection were compared between native and non-native populations of Neogobius kessleri Günther; introduced only within the interconnected Danube and Rhine River system, and N. melanostomus (Pallas); widely introduced throughout several river systems in Europe and North America. Higher values of Fulton’s condition factor were observed in non-native populations of both goby species. Neogobius melanostomus attained higher gonadosomatic index values in non-native populations, indicating potential increased investment in reproduction in its new area. A lower splenosomatic index was observed in non-native populations, especially in N. melanostomus. Parasite infracommunity richness and mean abundance were higher in N. kessleri in both native and non-native populations, suggesting higher susceptibility of N. kessleri to these parasites. Non-native populations of both hosts showed higher infra-community richness as a result of acquiring parasites native to the new area, but lower parasite abundance. Differences in success of the introduction and establishment in new areas between the two fish species may be associated with a relatively low parasite infection rate and a higher gonadosomatic index in non-native populations of N. melanostomus in comparison to N. kessleri.
Similar content being viewed by others
References
Brown CR, Brown MB (2002) Spleen volume varies with colony size and parasite load in a colonial bird. Proc R Soc Lond B 269:1367–1373
Bush AO, Lafferty KD, Lotz JM, Shostak AW (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. J Parasitol 83:575–583
Camp JW, Blaney LM, Barnes DK (1999) Helminths of the Round Goby, Neogobius melanostomus (Perciformes: Gobiidae), from Southern Lake Michigan, Indiana. J Helm Soc Wash 66:70–72
Copp GH, Bianco PG, Bogutskaya N, Erős T, Falka I, Ferreira MT, Fox MG, Freyhof J, Gozlan RE, Grabowska J, Kováč V, Moreno-Amich R, Naseka AM, Peňáz M, Povž M, Przybylski M, Robillard M, Russell IC, Stakėnas S, Šumer S, Vila-Gispert A, Wiesner C (2005) To be, or not to be, a non-native freshwater fish? J Appl Ichthyol 21:242–262
Corkum LD, Sapota MR, Skora KE (2004) The round goby, Neogobius melanostomus, a fish invader on both sides of the Atlantic Ocean. Biol Inv 6:173–181
Devin S, Beisel J-N (2007) Biological and ecological characteristics of invasive species: a gammarid study. Biol Inv 9:13–24
Diggins TP, Kaur J, Chakarborti RK, DePinto JV (2002) Diet choice by the exotic round goby Neogobius melanostomus as influenced by prey motility and environmental complexity. J Great Lakes Res 28:411–420
Ergens R, Lom J (1970) Causative agents of fish diseases. Academia, Prague
Forseth T, Naesje TF, Jonsson B, Harsaker K (1999) Juvenile migration in brown trout: a consequence of energetic state. J Anim Ecol 68:783–793
Freyhof J, Huckstorf V (2006) Conservation and management of aquatic genetic resources: a critical checklist of German freshwater fishes. In: Annual Report 2005; Leibniz-Institute of Freshwater Ecology and Inland Fisheries. Seibt, Berlin, pp 113–126
Grigorovich IA, Colautti RI, Mills EL, Holeck K, Ballert AG, MacIsaac HJ (2003) Ballast-mediated animal introductions in the Laurentian Great Lakes: retrospective and prospective analyses. Can J Fish Aquat Sci 60:740–756
Hanski I (1982) Dynamics of regional distribution: the core and satellite species hypothesis. Oikos 38:210–221
Jurajda P, Černý J, Polačik M, Valová Z, Janáč M, Blažek R, Ondračková M (2005) The recent distribution and abundance of non-native Neogobius fishes in the Slovak section of the River Danube. J Appl Ichthyol 21:319–323
Kvach J, Skóra KE (2007) Metazoa parasites of the invasive round goby Apollonia melanostoma (Neogobius melanostomus) (Pallas) (Gobiidae: Osteichthyes) in the Gulf of Gdansk, Baltic Sea, Poland: a comparison with the Black Sea. Par Res 100:767–774
Kvach J, Stepien CA (2008) Metazoan parasites of introduced round and tubenose gobies in the Great Lakes: support for the “Enemy Release Hypothesis”. J Great Lakes Res 34:23–35
L’avrinčíková M, Kováč V (2007) Invasive round goby Neogobius melanostomus from the Danube mature at small size. J Appl Ichthyol 23:276–278
Møller AP, Dufva R, Erritzøe J (1998) Host immune function and sexual selection in birds. J Evol Biol 11:703–719
Moravec F, Taraschewski H (1988) Revision of the genus Anguillicola Yamaguti, 1935 (Nematoda, Anguillicolidae) of the swimbladder of eels, including descriptions of 2 new species, Anguillicola novaezelandiae sp. n. and Anguillicola papernai sp. n. Folia Parasitol 53:125–146
Moyle PB (1986) Fish introductions into North America: patterns and ecological impact. In: Mooney HA, Drake JA (eds) Ecology of biological invasions of North America and Hawaii. Springer, New York
Ondračková M, Dávidová M, Pečínková M, Blažek R, Gelnar M, Valová Z, Černý J, Jurajda P (2005) Metazoan parasites of Neogobius fishes in the Slovak section of the River Danube. J Appl Ichthyol 21:349–354
Ondračková M, Dávidová M, Blažek R, Gelnar M, Jurajda P (2009) The interaction between an introduced fish host and local parasite fauna: Neogobius kessleri in the middle Danube River. Par Res 105:201–208
Polačik M, Janáč M, Trichkova T, Vassilev M, Keckeis H, Jurajda P (2008) The distribution and abundance of the Neogobius fishes in their native range (Bulgaria) with notes on the non-native range in the Danube River. Archiv Hydrobiol Suppl. Large Rivers 18:193–208
Polačik M, Janáč M, Jurajda P, Adámek Z, Ondračková M, Trichkova T, Vassilev M (2009) Invasive gobies in the Danube: invasion success facilitated by availability and selection of superior food resources. Ecol Fresh Fish 18:640–649
Prenter J, MacNeil C, Dick JTA, Dunn AM (2004) Roles of parasites in animal invasions. Trends Ecol Evol 19:385–390
Pronin NM, Fleischer GW, Baldanova DR, Pronina SV (1997) Parasites of the recently established round goby (Neogobius melanostomus) and tubenose goby (Proterorhinus marmoratus) (Cottidae) from the St. Clair River and Lake St. Clair, Michigan, USA. Folia Parasitol 44:1–6
Rokicki J, Rolbiecki L (2002) Colonization of the round goby, Neogobius melanostomus (Gobiidae) parasites in the new environment of the gulf of Gdaňsk (Southern Baltic). Wiadom Parazytol 48:197–200
Sasal P, Morand S, Guégan JF (1997) Determinants of parasite species richness in Mediterranean marine fishes. Mar Ecol Prog Ser 149:61–71
Simberloff D, Gibbons L (2004) Now you see them, now you don’t!–population crashes of established introduced species. Biol Inv 6:161–172
Skarstein F, Folstad I, Liljedal S (2001) Whether to reproduce or not: immune suppression and costs of parasites during reproduction in the Arctic char. Can J Zool 79:271–278
Stepien CA, Tumeo MA (2006) Invasion genetics of Ponto-Caspian gobies in the Great Lakes: a “cryptic” species, absence of founder effects, and comparative risk analysis. Biol Inv 8:61–78
Taraschewski H (2000) Host-parasite interactions in Acanthocephala: a morphological approach. Adv Parasitol 46:1–179
Tompkins DM, Begon M (1999) Parasites can regulate wildlife populations. Par Today 15:311–313
Torchin ME, Lafferty KD, Kuris AM (2001) Release from parasites as natural enemies: increased performance of a globally introduced marine crab. Biol Inv 3:333–345
Torchin ME, Lafferty KD, Dobson AP, McKenzie VJ, Kuris AM (2003) Introduced species and their missing parasites. Nature 421:628–630
Vila-Gispert A, Alcaraz C, García-Berthou E (2005) Life-history traits of invasive fish in small Mediterranean streams. Biol Inv 7:107–116
Wiesner C (2005) New records of non-indigenous gobies (Neogobius sp.) in the Austrian Danube. J Appl Ichthyol 21:324–327
Williams H, Jones A (1994) Parasitic worms of fish. Taylor and Francis, London
Acknowledgements
This study was supported by Ichthyoparasitology, Centre of Excellence No. LC 522. We would like to thank staff of the National Park Donau-Auen for sampling permission, Teodora Trichkova, Milen Vassilev, Jaroslav Černý and Hubert Keckeis for help with fish sampling; Zdenka Valová, Radim Blažek, Markéta Dušková and Karolína Rohlenová for help with parasite dissections, Martin Reichard for useful comments and Carl Smith and Seth White for English correction.
Author information
Authors and Affiliations
Corresponding author
Appendix
Appendix
See Table 5.
About this article
Cite this article
Ondračková, M., Francová, K., Dávidová, M. et al. Condition status and parasite infection of Neogobius kessleri and N. melanostomus (Gobiidae) in their native and non-native area of distribution of the Danube River. Ecol Res 25, 857–866 (2010). https://doi.org/10.1007/s11284-010-0716-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11284-010-0716-0