Abstract
The occurrence of Tylodelphys barilochensis, Acanthostomoides apophalliformis, Contracaecum sp. and Camallanus corderoi infecting Galaxias maculatus ("puyenes") was quantified for the first time in Lake Nahuel Huapi, southern Argentina. T. barilochensis was recorded in this lake for the first time. The role of G. maculatus population in transmission of parasites to the salmonids is more important for Contracaecum sp. (prevalence 14-34%) and A. apophalliformis (prevalence 30-54%) than for C. corderoi (prevalence 6-8%). The absence of Diphyllobothrium spp. in samples shows that the G. maculatus population does not play any role in the life cycles of these important zoonotic parasites. The sex of the host had no effect on T. barilochensis abundance. Statistical differences in T. barilochensis abundance between "puyenes" of the same size class between sampling stations and positive correlation between prevalence of infected snails and T. barilochensis abundance in fish suggest that different stocks have been sampled. Factors influencing T. barilochensis abundance are discussed.
parasitism; Tylodelphys; Galaxias maculatus; salmonids; southern Argentina
Infections by Helminth Parasites in "Puyenes", Galaxias maculatus (Galaxiidae, Salmoniformes), from Southern Argentina with Special Reference to Tylodelphys barilochensis (Digenea, Platyhelminthes)
Vol. 94(5): 605-609
J Revenga+, P Scheinert
Laboratorio de Ictiopatología, Centro Regional Universitario Bariloche, Unidad Postal Universidad Nacional del Comahue, 8400 Bariloche, Argentina
The occurrence of Tylodelphys barilochensis, Acanthostomoides apophalliformis, Contracaecum sp. and Camallanus corderoi infecting Galaxias maculatus ("puyenes") was quantified for the first time in Lake Nahuel Huapi, southern Argentina. T. barilochensis was recorded in this lake for the first time. The role of G. maculatus population in transmission of parasites to the salmonids is more important for Contracaecum sp. (prevalence 14-34%) and A. apophalliformis (prevalence 30-54%) than for C. corderoi (prevalence 6-8%). The absence of Diphyllobothrium spp. in samples shows that the G. maculatus population does not play any role in the life cycles of these important zoonotic parasites. The sex of the host had no effect on T. barilochensis abundance. Statistical differences in T. barilochensis abundance between "puyenes" of the same size class between sampling stations and positive correlation between prevalence of infected snails and T. barilochensis abundance in fish suggest that different stocks have been sampled. Factors influencing T. barilochensis abundance are discussed.
Key words: parasitism - Tylodelphys - Galaxias maculatus - salmonids - southern Argentina
Salmonid fishing is of economic importance in the Argentinian Patagonia.
The "puyen" Galaxias maculatus (Galaxiidae, Salmoniformes) is a small autochthonous fish (total asymptotic growth length = 97 mm in Ezquerra pond, near Lake Nahuel Huapi), (Cervellini et al. 1993) that inhabits southern South America and Oceania (Quaggiotto & Valverde 1993) and may be predated by salmonids whereby transmission of parasites may occurr (Revenga 1993). Studies in New Zealand (McDowall 1968) and Australia (Pollard 1971) agree that most of each population dies during its first year, immediately after spawning, but a small proportion might reach 3 years of age.
In a population study in a dam in North Patagonia, Ferriz (1987) observed an annual cycle. The "puyenes" are found in Patagonia in various lakes and rivers where they inhabits littoral waters.
Different helminth parasites have been recorded in "puyenes" from the Nahuel Huapi Lake (Ortubay et al. 1994) and information on their biology appears in articles by Szidat and Nani (1951), Szidat (1956), and Torres et al. (1990).
Tylodelphys is a digenetic trematode genus and its species range extensively in both the northern and southern hemispheres. The species paraziting "puyenes" that have been described for the region are T. argentinus, T. barilochensis and T. crubensis (Quaggiotto & Valverde 1992). Adults develop in the intestine of ichthyophagous birds (species unknown for the region). The first stage (miracidium) is a swimming larva. The following stages (sporocysts, rediae, cercariae) develop in snails (Chilina sp.).When the cercariae emerge, they can swim and actively infect "puyenes", where the metacercariae develop (Scheinert et al. 1997).
This paper presents the first quantitative parasitological records of "puyenes" from Nahuel Huapi Lake and analyses species abundance of T. barilochensis and migratory movements of fishes.
The study was carried out in Lake Nahuel Huapi, in the Nahuel Huapi National Park and Reserve (40°8'-41°35'S, 71°2'-71°57'W). The coastline is very irregular with a series of bays, peninsulas, and isthmuses, gravel or sandy beaches, and rocky cliffs, favouring the existence of different microhabitats. The lake bed harbors few macrophytes, partly because of the low proportion of shallow waters and partly because of wave action, strongly influenced by west winds (Thomasson 1959). The town of San Carlos de Bariloche is located on the easthern coast.
Six sampling stations were established on the easthern littoral zone over aproximately 40 km (named A, B, C, D, E and F). Distance from the town of San Carlos de Bariloche increases from A (0 km) to F (40 km). From January 20 to February 10, 1994, 579 "puyenes" G. maculatus, were trapped (Table I). Traps were submerged at a depth not greater than 0.5 m for 1-5 days. After not longer than five days, fish were put to death, total length and weight were measured and sex was determined (162 males and 154 females; the remaining fish were inmature). Necropsies were carried out under stereomicroscope and internal helminth parasites collected, identified and counted.
On February 12 and 13, 1994, Chilina dom-beiana snails were sampled from the Nahuel Huapi stations where fish were captured. Random samples were taken (manual collection within an area of 1 m²) every 4 m along a transect of approximately 150 m, at a depth between 0.0 and 0.40 m. From each sample, 70 snails were separated at random in individual glasses at room temperature, to observe cercariae emergence. The cercariae that emerged were "furcocercaria type A" and "echinocercaria sp.", as described by Ostrowsky and Quaggiotto (1995), but never coexisted. Absence of trematode larvae was verified by necropsy under stereomicroscope for snails that failed to shed cercariae. Specific identity of cercariae was determined by experimental infections with "furcocer-caria type A" on "puyenes" free of parasites, as in Scheinert et al. (1997). They were found to correspond to T. barilochensis (Quaggiotto & Valverde 1992).
In this paper, the terms abundance and prevalence are used according to the recommendations of Margolis et al. (1982).
The Mann-Whitney, Kruskall-Wallis and multiple comparison (Conover 1980) tests were used to compare abundances. Correlation analysis was used to relate prevalence of infected snails and parasite abundance in fish and density of snails and parasite abundance in fish. The significance level considered was 0.05.
Table I shows the number of "puyenes" of different size classes captured at the different sampling stations.
The following parasites were found: T. barilochensis (unencysted metacercariae in the encephalic cavity), A. apophalliformis (metacercariae encysted in the liver), Contracaecum sp. (larvae in the body cavity) and C. corderoi (adults in intestine). Table II shows abundance and prevalence of the parasites found at the different sampling stations.
For T. barilochensis, no significant difference in parasite abundance was found between fish sexes. The analysis of T. barilochensis metacercariae abundance for each "puyenes" size class showed significant differences between sites for size classes 41-50, 51-60 and > 60 mm (Kruskall-Wallis test). Comparing abundance in pairs (a posteriori), the multiple comparison test permits a distinction of fish as follows (Fig.1), in size class 41-50 mm 3 stocks (A, B-E, C-D). In size class 51-60 mm 3 stocks (B-E, C, F) and in size class > 60 mm 3 stocks (B, E, F). Increased abundance with fish size and stocks of fish is also shown (Fig. 1). Fig. 2 shows positive correlation between prevalence of snails infected by T. barilochensis and parasite abundance in fish of 3 size classes (41-50, 51-60, > 60 mm), r²= 0.98, r²= 0.96 and r²= 0.79 respectively. In contrast, Fig. 3 shows no correlation between density of snails and abundance of parasites in fish of size classes 41-50, 51-60 and > 60 mm; r²= 0.44, r² = 0.40 and r² = 0.41.
This is the first time that the presence of T. barilochensis, A. apophalliformis, Contracaecum sp. and C. corderoi in G. maculatus is quantified in the Nahuel Huapi National Park and Reserve. It is also the first time that T. barilochensis has been recorded in "puyenes" from Lake Nahuel Huapi. To date, it is the most abundant parasite reported from fish in the entire Park.
The final hosts of Tylodelphys spp. are birds. For A. apophalliformis, Contracaecum sp. and C. corderoi fish may act both as intermediate and definitive hosts, thus transmission by predation may occurr. This mechanism has been proposed for G. maculatus and salmonids for Contracaecum sp. and C. corderoi, in Chile (Torres et al. 1991). According to our results, the role of G. maculatus population in transmission of parasites to the salmonids is more important for Contracaecum sp. (prevalence 14-34%) and A. apophalliformis (prevalence 30-54%) than for C. corderoi (prevalence 6-8%). Revenga (1993) reports two parasites with zoonotic importance: Diphyllobothrium dendriticum and D. latum in fish from Lake Moreno, which is connected with Nahuel Huapi Lake. He suggests that salmonids can act as paratenic hosts for both species and states the importance of studying the role of G. maculatus populations in the life cycle of D. dendriticum and D. latum. The absence of Diphyllobothrium spp. in this study shows that the G. maculatus population does not play a role in life cycles of these parasites and contradicts the argument of salmonids as paratenic hosts.
The absence of significant differences in. T. barilochensis abundance between sexes shows that susceptibility to infection is not associated with sex.
The use of parasites for separating fish stocks has been reviewed by different authors (MacKenzie l983, l987, Lester 1990). In this study the absence of Contracaecum sp. and C. corderoi at stations A, B and D suggests different fish stocks. The significant differences in the abundance of T. barilochensis from fish in the same size (as age indicator) class from neighbouring stations (Fig. 1) reinforces the hypothesis of different stocks. When more than one size class repeats the same result (Fig.1) this idea is further reinforced. The positive correlation between metacercariae abundance and prevalence of infected snails (also analyzed by size class in "puyenes") at different stations (Fig. 2), constitutes additional information in favor of this hypothesis. All these results strongly suggest that different stocks have been sampled, although this does not exclude the possibility of a certain degree of mixing, which is difficult to quantify (Lester 1990).
This stock separation in small fishes with short lives (Gambusia affinis) was observed by Aho et al. (1982) and Camp et al. (1982) in studies on population biology of metacercariae of the family Diplostomatidae. The Lake Nahuel Huapi receives urban contaminants at some points. If the movement of fishes from place to place were restricted and certain stocks remained permanently in contaminated areas, the effect of contamination on fishes could be studied. Further studies including more sampling stations, greater sample size and analyses of water quality would be of interest.
The lack of correlation between density of snails and T. barilochensis metacercariae abundance in fishes analyzed by size class suggests that it is prevalence rather than number of previous hosts, that regulates parasite abundance in fishes. Thus, the controlling factor would be number of birds (definitive hosts) that visit or remain in different areas of the lake. Further studies are needed.
To Eduardo Revenga for help with data processing and Clive R Kennedy for helpful criticism on a previous version of this paper.
Fig.1 | Fig.2 | Fig.3 | TABLE I | TABLE II
This project was partially supported by grant No. B029 from Universidad Nacional del Comahue.
+Corresponding author. Present address: Depto. de Acuicultura, CRUB, Universidad Nacional del Comahue, Quintral 1250, 8400 Bariloche, Argentina. Fax: +54-944-22111. E-mail: jrevenga@bariloche.com.ar
Received 26 August 1998
Accepted 19 May 1999
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Publication Dates
-
Publication in this collection
27 Aug 1999 -
Date of issue
Sept 1999
History
-
Received
26 Aug 1998 -
Accepted
19 May 1999