Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-27T08:02:15.406Z Has data issue: false hasContentIssue false
  • English
  • Français

Geographic and ontogenetic variations in parasite communities of intertidal fish species from the south-eastern Pacific coast

Published online by Cambridge University Press:  07 February 2020

N.V. Leiva Open the ORCID record for N.V. Leiva [Opens in a new window] ,
G. Muñoz  and
M.T. González
N.V. Leiva*
Affiliation:
Instituto de Ciencias Naturales ‘Alexander von Humboldt’, Facultad de Ciencias del Mar y Recursos Biológicos, Universidad de Antofagasta, Antofagasta, Chile
G. Muñoz
Affiliation:
Facultad de Ciencias del Mar y de Recursos Naturales, Universidad de Valparaíso, Viña del Mar, Chile
M.T. González
Affiliation:
Instituto de Ciencias Naturales ‘Alexander von Humboldt’, Facultad de Ciencias del Mar y Recursos Biológicos, Universidad de Antofagasta, Antofagasta, Chile
*
Author for correspondence: N.V. Leiva, E-mail: natalialeivah.uv@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Parasite composition can be affected by physiological and ecological changes during host ontogeny. Intertidal fish do not travel long distances and live in the same area throughout their lifetimes, meaning that parasite communities can differ across geographic ranges. The objective of this study was to analyse the parasite communities of three fish species (Hypsoblennius sordidus, Helcogrammoides cunninghami and Scartichthys viridis) collected from the Chilean coast. The composition of parasite species was compared among host ontogenetic stages (larvae, juveniles and mature fish) and geographic areas. A total of 184 larval, 252 juveniles and 217 mature individuals were collected in the northern area (c. 24°S), and 186 larval, 192 juveniles and 112 mature individuals from the central area (c. 33°S). Ectoparasites were most prevalent in fish from the central area, whereas endoparasites were most prevalent in the northern area. The parasite species richness varied significantly between geographical areas for H. sordidus and H. cunninghami, but the parasite composition varied significantly between geographical areas for all fish species analysed. Therefore, the geographical area was the most important factor determining the parasite composition of intertidal fish species. The absence of endoparasites in fish larvae and the increased infestation in juvenile and mature fish may be explained by the shift in habitat from the water column to intertidal pools where prey abundance and availability are higher. On the other hand, hydrographic barriers affecting prey distributions may also offer an explanation as to the differences in parasite composition.

Keywords

Biogeographyfishesintertidal rocky zoneontogenyparasites
Type
Short Communication
Information
Journal of Helminthology , Volume 94 , 2020 , e124
Copyright
Copyright © The Author(s) 2020. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Balbontín, F and Pérez, R (1979) Modalidad de postura, huevos y estados larvales de Hypsoblennius sordidus (Bennett) en la Bahía de Valparaíso (Blenniidae: Perciformes). Revista de Biología Marina 16, 1–318.Google Scholar
Bush, AO, Lafferty, KD, Lotz, JM and Shostak, AW (1997) Parasitology meets ecology in its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575–583.CrossRefGoogle Scholar
Camus, PA (2001) Biogeografía marina de Chile continental. Revista Chilena de Historia Natural 74, 587–617.CrossRefGoogle Scholar
Cancino, C, Farías, K, Lampas, S, González, B and Cuevas, V (2010) Descripción de los complejos estructurales óseos en Helcogrammoides chilensis (Blennioidei: Tripterygiidae) de la zona central de Chile. Revista de Biología Marina y Oceanografía 45, 671–682.CrossRefGoogle Scholar
Cribb, TH (2005) Family opecoelidae. pp. 443–532in Jones, A, Bray, RA and Gibson, DI (Eds) Keys to the Trematoda. London, CABI Publishing.CrossRefGoogle Scholar
Escribano, R, Marín, V and Irribarren, C (2000) Distribution of Euphausia mucronata at the upwelling area of Peninsula Mejillones, northern Chile: the influence of the oxygen minimum layer. Scientia Marina 64, 69–77.CrossRefGoogle Scholar
Flores, K and George-Nascimento, M (2009) Las infracomunidades de parásitos de dos especies de Scartichthys (Pisces: Blenniidae) en localidades cercanas del norte de Chile. Revista Chilena de Historia Natural 82, 63–71.CrossRefGoogle Scholar
González, MT and Moreno, CA (2005) The distribution of the ectoparasite fauna of Sebastes capensis from the southern hemisphere does not correspond with zoogeographical provinces of free-living marine animals. Journal of Biogeography 32, 1539–1547.CrossRefGoogle Scholar
González, MT and Oliva, ME (2009) Is the nestedness of metazoan parasite assemblages of marine fishes from the southeastern Pacific coast a pattern associated with the geographical distributional range of the host? Parasitology 136, 401–409.CrossRefGoogle Scholar
González, MT and Poulin, R (2005) Spatial and temporal predictability of the parasite community structure of a benthic marine fish along its distributional range. International Journal for Parasitology 35, 1369–1377.CrossRefGoogle ScholarPubMed
González, MT, Barrientos, C and Moreno, CA (2006) Biogeographical patterns in endoparasite communities of a marine fish (Sebastes capensis Gmelin) with extended range in the Southern Hemisphere. Journal of Biogeography 33, 1086–1095.CrossRefGoogle Scholar
Guiñez, M, Valdés, J and Sifeddine, A (2010) Variabilidad espacial y temporal de la materia orgánica sedimentaria, asociada a la Zona de Mínimo Oxígeno (ZMO), en un ambiente costero del norte de la corriente de Humboldt, bahía de Mejillones, Chile. Latin American Journal of Aquatic Research 38, 242–253.CrossRefGoogle Scholar
Hernández, CE, Neill, PE, Pulgar, JM, Ojeda, FP and Bozinovic, F (2002) Water temperature fluctuations and territoriality in the intertidal zone: two possible explanations for the elevational distribution of body size in Graus nigra. Journal of Fish Biology 61, 472–488.CrossRefGoogle Scholar
Hernández, CE, Moreno, RA and Rozbaczylo, N (2005) Biogeographical patterns and Rapoport's rule in southeastern Pacific benthic polychaetes of the Chilean coast. Ecography 28, 363–373.CrossRefGoogle Scholar
Jones, A and Bray, RA (1994) Keys to the cestode parasites of vertebrates. 751 pp. Wallingford, Cab International.Google Scholar
Landaeta, MF, Contreras, JE, Bustos, CA and Muñoz, G (2015) Larval growth of two species of lanternfish at nearshore waters from an upwelling zone based on otolith microstructure analyses. Journal of Applied Ichthyology 31, 106–113.CrossRefGoogle Scholar
Leiva, N, George-Nascimento, M and Muñoz, G (2015) Carga parasitaria en crustáceos decápodos de la costa central de Chile: ¿Existe alguna asociación con la abundancia de los hospedadores definitivos? Latin American Journal of Aquatic Research 43, 726–738.Google Scholar
Leiva, NV, López, Z, González, MT and Muñoz, G (2017) Determining intermediate hosts for Opecoelidae and Microphallidae species (Platyhelminthes: Trematoda) in the Southeastern Pacific Coast, using molecular markers. Journal of Parasitology 103, 132–138.CrossRefGoogle ScholarPubMed
Mansur, L, Plaza, G, Landaeta, MF and Ojeda, FP (2014) Planktonic duration in fourteen species of intertidal rocky fishes from the south-eastern Pacific Ocean. Marine and Freshwater Research 65, 901–909.CrossRefGoogle Scholar
Medina, M, Vega, AC and Araya, CM (2004) Guía de peces marinos de la zona norte de Chile. 104 pp. Iquique, Universidad Arturo Prat.Google Scholar
Moravec, F (1998) Nematodes of freshwater fishes of the Neotropical region. 464 pp. Prague, Academia Publishing House of the Academy of Sciences of the Czech Republic.Google Scholar
Muñoz, G and Delorme, N (2011) Variaciones temporales de las comunidades de parásitos en peces intermareales de Chile central: hospedadores residentes vs temporales. Revista de Biología Marina y Oceanografía 46, 313–327.CrossRefGoogle Scholar
Muñoz, AA and Ojeda, FP (1997) Feeding guild structure of a rocky intertidal fish assemblage in central Chile. Environmental Biology of Fishes 49, 471–479.CrossRefGoogle Scholar
Muñoz, G and Randhawa, HS (2011) Monthly variation in the parasite communities of the intertidal fish Scartichthys viridis (Blenniidae) from central Chile: are there seasonal patterns? Parasitology Research 109, 53–62.CrossRefGoogle ScholarPubMed
Muñoz, G and Zamora, L (2011) Ontogenetic variation in parasite infracommunities of the clingfish Sicyases sanguineus (Pisces: Gobiesocidae). Journal of Parasitology 97, 14–20.CrossRefGoogle Scholar
Muñoz, G, Valdebenito, V and George-Nascimento, M (2002) La dieta y la fauna de parásitos metazoos del torito Bovichthys chilensis Regan 1914 (Pisces: Bovichthydae) en la costa de Chile centro-sur: variaciones geográficas y ontogenéticas. Revista Chilena de Historia Natural 75, 661–671.CrossRefGoogle Scholar
Ojeda, F, Labra, F and Muñoz, A (2000) Biogeographic patterns of Chilean littoral fishes. Revista Chilena de Historia Natural 73, 625–641.CrossRefGoogle Scholar
Oliva, ME and González, MT (2005) The decay of similarity over geographical distance in parasite communities of marine fishes. Journal of Biogeography 32, 1327–1332.CrossRefGoogle Scholar
Pequeño, G (2000) Delimitaciones y relaciones biogeográficas de los peces del Pacífico Suroriental. Estudios Oceanológicos 19, 53–76.Google Scholar
Petrochenko, VI (1958) Acanthocephala of domestic and wild animals. Vol. II, 458 pp. Moscú, Izdatelstvo Akademii Nauk SSSR.Google Scholar
Poulin, R (2007) Evolutionary ecology of parasites. 332 pp. Princeton, New Jersey, Princeton University Press.Google Scholar
Pulgar, JM, Bozinovic, F and Ojeda, FP (2005) Local distribution and thermal ecology of two intertidal fishes. Oecologia 142, 511–520.CrossRefGoogle ScholarPubMed
Pulgar, JM, Bozinovic, F and Ojeda, FP (2007) Inter-population thermal variability and physiological response in the intertidal fish Scartichthys viridis (Blenniidae). Revista Chilena de Historia Natural 80, 439–446.CrossRefGoogle Scholar
Ritter, AF (2017) Adult avoidance behavior leads to ontogenetic shifts in habitat use of an intertidal fish. Marine Ecology Progress Series 585, 143–154.CrossRefGoogle Scholar
Stepien, CA (1990) Population structure, diets and biogeographic relationships of a rocky intertidal fish assemblage in central Chile: high levels of herbivory in a temperate system. Bulletin of Marine Science 47, 598–612.Google Scholar
Valdovinos, C, Navarrete, SA and Marquet, PA (2003) Mollusk species diversity in the Southeastern Pacific: why are there more species towards the pole? Ecography 26, 139–144.CrossRefGoogle Scholar
Venables, WN and Ripley, BD (2002) Modern applied statistics with S. 330 pp. New York, Springer.CrossRefGoogle Scholar
Supplementary material: File

Leiva et al. supplementary material

Tables S1-S3

Download Leiva et al. supplementary material(File)
File 23.2 KB