Free Access
Issue
Aquat. Living Resour.
Volume 31, 2018
Article Number 29
Number of page(s) 6
DOI https://doi.org/10.1051/alr/2018019
Published online 10 October 2018

© EDP Sciences 2018

1 Introduction

European grayling Thymallus thymallus L. is a valuable fish species widely distributed in the Central and Northern Europe but is dependent on water of excellent quality with low temperature and high oxygen content. Deterioration of the aquatic environment including low water quality, changes in river morphology and flow regime, spawning grounds destruction, overfishing by sport anglers, and predation have considerably decreased grayling populations in the majority of European waters (Magee, 1993; Northcote, 1995; Uiblein et al., 2001). Despite its status on the European IUCN Red List of Threatened Species as “least concern” (Freyhof, 2011; Freyhof and Brooks, 2011), the status in the Czech Republic is “near threatened” (Lusk et al., 2004), “vulnerable” in France (UICN France et al., 2010) and Austria (Wolfram and Mikschi, 2007), “threatened” in Switzerland (Kirchhöfer et al., 2007), and “endangered” in Germany (Freyhof, 2009). Gum et al. (2006) reported cessation of European grayling stocking programs and a continued relatively low level of captive breeding programmes and support for breeding until ongoing cormorant and goosander predation problems are resolved. There are currently several programs in the Czech Republic aimed at restoring extinct grayling populations (Czech Anglers' Union, personal communication).

To re-establish threatened and extinct populations and expand the recreational fishery, hatchery-reared fish are commonly stocked. The success of stocking fish into natural waters depends on a variety of factors including fish origin, conditioning and acclimatization, handling and transportation, stocking density, and size and age, as well as timing of stocking and predation (Cowx, 1994). Destruction of wild grayling populations, often used as broodfish reservoirs, leads to insufficient local stock, forcing managers of fishing grounds to purchase and stock fish from producers outside the region. Some reports indicate problems with non-local fish. Johnsen and Hesthagen (1990) reported higher recapture rates of brown trout stocked into streams near their rearing site than into distant areas. Stress of transportation may result in lower survival, growth, and fecundity of stocked salmonids compared to resident wild fish (Jonsson et al., 1999; Finstad et al., 2003). Although some authors have pointed to the risk of genetic disruption in local grayling populations when stocking trans-basin fish (Meraner et al., 2013; Weiss et al., 2013), the use of extrinsic stock is often the only possibility for re-establishing deteriorating and depleted grayling populations.

The aim of this study was to investigate the effect of geographic origin and transport of fish on their post-stocking performance by assessing recapture rates of hatchery-reared 1+ year-old T. thymallus from one local and two distant hatcheries released into the Blanice River in South Bohemia, Czech Republic.

2 Materials and methods

2.1 Study area

The Blanice River (Vltava basin) in South Bohemia is 93 km long, with a drainage area of 860 km2. Six release sites of 150–190 m were designated in a 5 km stretch of the river (river km 53–58) in a protected area (fishing prohibited) downstream of the Husinec reservoir (37 ha; 2.5 × 106 m3) (Fig. 1). The Husinec reservoir provides a drinking water supply, flood protection, and hydroelectric power without hydropeaking. Water flow in this stretch of the river is characterized by wide seasonal fluctuations depending on rainfall, with an annual mean flow of 3.5 m3 s−1. During May–October 2014, the mean flow was 2.5 ± 1.8 m3 s−1 (min. 0.5, max. 6.3 m3 s−1), the mean water temperature was 12.5 ± 3.5 °C, and pH was 7–7.8. These values, and the water conductivity of 180–240 µS cm−1, are typical for the Blanice River in this season. The release sites were in an area of broad-leaf trees and meadows at ∼500 m asl. The sites had natural gravel banks and were similar with respect to substrate (gravel and stones), area (about 2000 m2), and water velocity. The borders of sections consisted of natural shallow gravel riffles, making fish migration difficult and were ideal for installation of pulsed-DC electrofishing units as a barrier to escape from the sites during electrofishing sampling. Depth ranged from 10–80 cm and width from 7–11 m in all sites. The dominant fish species in the area are brown trout Salmo trutta m. fario L. and grayling. European bullhead Cottus gobio L., stone loach Barbatula barbatula L., roach Rutilus rutilus L., and gudgeon Gobio gobio L. were caught occasionally. The sites were under severe predation pressure from the great cormorant Phalacrocorax carbo throughout several winters beginning in 2008/9. Therefore, we supposed strong reduction of fish (especially grayling) populations in all sites.

thumbnail Fig. 1

Map showing the locations of release sites in the Blanice River. The inset shows location hatcheries producing the fish used in the survey.

2.2 Fish

Hatchery-reared grayling were randomly chosen from one-year-old fish reared on conventional dry food pellets from fingerlings in concrete tanks at the Husinec, Pardubice, and Hynčice hatcheries.

Fish from the Husinec Hatchery (Czech Anglers' Union) were progeny of resident wild broodstock from the Blanice River (hand stripped). The hatchery is supplied with water from the Blanice River and is 5–7 km from the release sites.

Hynčice and Pardubice fish were transported on 12 May 2014 to the Research Institute of Fish Culture and Hydrobiology in Vodňany. The Pardubice hatchery (Czech Anglers' Union), at ∼220 m asl, is supplied with water from the Loučná River in East Bohemia (Labe basin) and is 250 km from the release sites (Fig. 1). The fish were progeny of resident wild broodstock of the Loučná River (hand stripped). The Loučná River is 81 km long with a drainage area of 724 km2. The fish were transported in an aerated plastic tank, and duration of transport was approximately 3 h.

The Hynčice hatchery, at an elevation of ∼420 m asl, is supplied with water from the Stěnava River in north-east Bohemia (Odra basin) and is 300 km from the release sites (Fig. 1). The Stěnava River is 62 km long with a drainage area of 594 km2. Fish from this hatchery were progeny of wild broodfish originating from the Metuje River (Labe basin). The fish were transported in three plastic bags with oxygenated water, and duration of transport was about 4 h. Fish were held overnight (∼15 h) at the Research Institute of Fish Culture and Hydrobiology in aerated 400 l aquaria in tap water until release.

2.3 Release

In their respective hatcheries prior to transport, fish were anaesthetized with 2-phenoxy-ethanol (0.2 ml l−1), and Visible Implant Elastomer (VIE) tags (Northwest Marine Technology, Ltd., USA), using a different colour for each source group, were injected in small quantities under the transparent skin behind the eye, on the mandible, and the operculum. Fish were tagged on either the left or right side of the head or mid-mandible and behind both eyes to identify them according to release site. The tags were injected twice in each position as a precaution against loss. Fish from the Husinec hatchery were randomly divided and tagged as Husinec Groups 1 and 2 according to co-released fish group (Tab. 1). Fifty fish from each hatchery were randomly chosen, measured (standard length LS, cm), and weighed (W, g) using a KERN Balance (type EMB 1200-1; max. 1200 g, d = 0.1 g) with a plastic bowl and measuring groove accurate to 1 mm. Fulton's condition factor (K = W/LS−3 × 100) was determined for each measured fish. After tagging, fish from the Husinec hatchery were placed in a flow-through system with water from the Blanice River in the hatchery area, and fish from Pardubice and Hynčice were placed in aquaria with tap water. The following morning (13 May), fish were transported to the release sites. Water from the Blanice River was used for the transport of fish from the Husinec groups in containers fitted with an oxygen injection system, and the duration of transport did not exceed 20 min. Tap water was used for transporting fish from the Hynčice and Pardubice groups in the same containers used for the Husinec groups, duration of transport was ∼30 min. Before release, water from the river was slowly mixed with water in transport containers. Each site was stocked with 100 fish from the Husinec hatchery along with 100 from Hynčice (sites I–III) or Pardubice (sites IV–VI) (Tab. 1). Fish were released in groups in the central area of each site. The total number of stocked fish was 1200.

Table 1

Number of grayling released at each site and tagging.

2.4 Recapture

Five months after release (20–21 October 2014), the sites and the stretches of river separating them, including approximately 1 km of the river downstream of the release area, were rigorously electrofished twice using two back-pack pulsed-DC electrofishing units (FEG 1500, EFKO-Germany). A further two backpack pulsed-DC electrofishing units (FEG 3000, EFKO-Germany) were situated at the upper border of each site to prevent fish from escaping upstream. All recaptured tagged fish were identified, measured, and weighed, and condition factor was determined. After measurement, fish from the Husinec groups were released near the point of capture, and fish from the Pardubice and Hynčice groups were released into a fishing area downstream of the surveyed area.

2.5 Statistical analyses

A one-way analysis of variance (ANOVA) was used to assess differences in weight, length, and K among fish groups prior to stocking and at recapture. Post hoc comparisons were made by Tukey's honest significant difference test. Student's t-test was used to test for weight, length, and K differences among groups of grayling stocked in the same sites. Recapture rates and movement of tagged fish were compared with the Pearson and maximum likelihood χ2 test. Significance was accepted for values of p < 0.05.

3 Results

Of the 1200 grayling tagged, 283 (23.6%) were recaptured. Wild grayling were occasionally captured, chiefly in the downstream areas (9 ind., SL 17–33 cm in Sites III–VI; 36 ind., SL 10–36 cm in Sites I and II). Higher density of brown trout in the lower river stretches was visually estimated during electrofishing. No significant differences in recapture rate were found between groups released within a given site (Sites I–III, Husinec 1, 22.0% v. Hynčice, 17.3%; Sites IV–VI, Husinec 2, 29.0% v. Pardubice, 26.0%), with the exception of Site V, which showed a significantly higher recapture rate (χ2 = 4.34; df = 1; p = 0.037) of local fish (Husinec 2, 33.0%) than distant strains (Pardubice, 20.0%).

Differences in recapture rate were found with respect to release site (χ2 = 12.78; df = 3; p = 0.005). Fish from the Hynčice group showed lower probability of being recaptured than fish released into upstream sites (IV–VI), Husinec 2 (p < 0.001) and Pardubice (p = 0.010). A significantly higher recapture rate of fish from Husinec 2 than Husinec 1 (p = 0.049) was also found.

Site fidelity, the recapture of marked fish in their original release site, was significantly higher (χ2 = 4.504; df = 1; p = 0.034) for Husinec 1 (11.7%) than for the Hynčice group (6.7%). Recapture downstream or upstream of release site did not differ among groups. Values of recapture rate are provided in Figure 2.

Significantly different weight (F = 20.61; df = 2; p < 0.001) and condition factor (F = 71.15; df = 2; p < 0.001) of fish before release were found among hatchery groups (Husinec groups combined). Initial SL of fish was higher (F = 23.83; df = 2; p < 0.001) in the Pardubice group than in Husinec and Hynčice groups (Tab. 2).

The weight and length of fish increased significantly in all groups over the course of the trial. Final weight and SL of groups released in the same site did not differ. Recaptured Husinec 2 and Pardubice fish were significantly heavier (F = 17.29; df = 3; p < 0.001) than other groups. Pardubice fish were also longer than fish from Husinec 1 and Hynčice at recapture (Tab. 3).

Significant differences (F = 14.89; df = 3; p < 0.001) were found in condition factor of recaptured fish. The Husinec 2 group exhibited higher K than the Pardubice group (p = 0.042). Final condition factor of fish from these two groups was significantly higher than fish from Husinec 1 (p < 0.001 vs. Husinec 2 and p = 0.029 vs. Pardubice) and Hynčice groups (p < 0.001 vs. Husinec 2 and p = 0.005 vs. Pardubice).

There were no significant differences in mean final weight, SL, and condition factor of fish groups released in the same site. Within each group, there were no differences in weight, SL, and condition among fish recaptured within, upstream, or downstream of their original release site.

thumbnail Fig. 2

Recapture rate (site fidelity = recapturing into release site/upstream = recapturing up of release site/downstream = recapturing down of release site) of stocked grayling in each site and total values (right column). *above bars indicates a significant difference (P < 0.05) in total recapture rate, different letters in bars indicate a significant difference (P < 0.05) in site fidelity/upstream/downstream recapture rate.

Table 2

Biometric data for tagged grayling before release: mean (±SD) standard length (LS), weight (W), and Fulton's condition factor (K).

Table 3

Biometric data for tagged grayling after recapture: mean (±SD) standard length (LS), weight (W), and Fulton's condition factor (K).

4 Discussion

The study demonstrated no significant advantage of stocking one-year-old European grayling from a local hatchery in comparison with strains from distant localities as assessed five months post-release. The higher recapture rate of local stock released in one site was not noted in the other two sites stocked with these strains.

With regard to the crucial time for fish adaptation immediately after stocking and during the first weeks in the wild (Heggberget et al., 1993; Olla et al., 1994, 1998; Brown and Laland, 2001), the five month period between stocking and recapture in our study should have been sufficient to provide information of adaptation to the Blanice River environment, including natural prey intake. Our results are contrary to the higher recapture rates of brown trout stocked into streams near their rearing site than in distant areas reported by Johnsen and Hesthagen (1990), who attributed the difference to factors associated with transportation but suggested that the impact of local climatic conditions and/or water chemistry could not be discounted. In the present study, transportation from distant hatcheries was 3–4 h in oxygenated plastic bags. During marking and overnight before release, fish were held in aquaria with tap water and aerating pumps typical for transportation. The local strains of fish were held in flow-through tanks with water from the stocked river. A negative effect of transportation time and conditions was not observed. However, equalization of the initially significantly lower weight and condition factor of Husinec fish compared with the non-local fish released into the same sites may indicate an advantage for local fish. It also agrees with the findings of Jonsson et al. (1999), who found better growth of brown trout acclimated prior to stocking compared to fish released directly. The lack of difference in downstream migration rate is consistent with results of Thorfve (2002) who reported no significant influence of the acclimatization period on downstream migration of stocked grayling.

The recapture rates observed in all groups of fish in the present study were higher than recapture rate of hatchery-reared, and similar to recapture rates of pond-reared, yearling grayling in Turek et al. (2012). This may be attributed to reduction of territorial competition between wild and stocked grayling attributed to scarcity of wild fish due to cormorant predation in the previous winters. The lower recapture of fish released into downstream sites (I–III) may be explained by higher competition from wild fish. These sites were near a village, where predation by cormorants may have been reduced, as suggested by the higher numbers of wild grayling and brown trout caught in these sections during electrofishing. Similarly, Hanfland and Laggerbauer (2011) observed fair grayling population in urban areas of rivers otherwise affected by cormorants, although other environmental parameters were suboptimal. Given the similar morphology of all sections, the influence of abiotic factors on lower performance in groups stocked in downstream section is unlikely. Hart et al. (2014) pointed to the importance of familiarity on adaptation to changing environmental conditions in grayling juveniles: fish paired with familiar partners were significantly more likely to enter and forage in new, upstream habitats with potentially reduced risk of predation. Hence, our strategy of stocking several fish groups into a single site may have improved the post-release performance and should be recommended for grayling management.

Some studies have pointed to a negative impact of non-autochthonous stock on the genetic structure of local grayling populations (Duftner et al., 2005; Dawnay et al., 2011; Weiss et al., 2013), especially for watersheds with preserved genetic structure and diversity of wild populations. Persat et al. (2016) suggested that stocking of grayling has provided no reproductive benefits to wild populations, due to low long-term survival of stocked fish. In the Czech Republic, populations of European grayling in the Elbe basin show low genetic variability and were strongly affected by introgressive gene flow caused by previous fishery management and restocking (Havelka, 2009; Havelka et al., 2013). The populations used in the present study were genetically similar, belonging to the east-central European group (Gum et al., 2005) of grayling populations. The results suggest the feasibility of using fish from remote hatcheries within the Elbe drainage in Czech Republic for restoration of threatened grayling populations without additional deterioration of genetic variation. After re-establishment of a naturally reproducing population, further management practices should be focused on the development of conditions for natural spawning and local stock production, based on a combination of intensive autochthonous broodstock production and wild fish exploitation, as suggested by Randák (2014).

Acknowledgments

The study was financially supported by the Ministry of Education, Youth and Sports of the Czech Republic − projects CENAKVA (No. CZ.1.05/2.1.00/01.0024), CENAKVA II (No. LO1205 under the NPU I program). The authors thank the Czech Anglers' Union and MVDr. Miroslav Kulich, owner of Hynčice hatchery, for technical support.

References

  • Brown C, Laland K. 2001. Social learning and life skills training for hatchery reared fish. J Fish Biol 59: 471–493. [CrossRef] [Google Scholar]
  • Cowx IG. 1994. Stocking strategies. Fish Manage Ecol 1: 15–130. [Google Scholar]
  • Dawnay N, Dawnay L, Hughes RN, Cove R, Taylor MI. 2011. Substantial genetic structure among stocked and native populations of the European grayling (Thymallus thymallus, Salmonidae) in the United Kingdom. Conserv Genet 3: 731–744. [CrossRef] [Google Scholar]
  • Duftner N, Koblmüller S, Weiss S, Medgyesy N, Sturmbauer C. The impact of stocking on the genetic structure of European grayling (Thymallus thymallus, Salmonidae) in two alpine rivers, in: Aquatic Biodiversity II, Springer, Netherlands, 2005, pp. 121–129. [CrossRef] [Google Scholar]
  • Finstad B, Iversen M, Sandodden R. 2003. Stress-reducing methods for releases of Atlantic salmon (Salmo salar) smolts in Norway. Aquaculture 222: 203–214. [CrossRef] [Google Scholar]
  • Freyhof J. 2009. Rote Liste der im Süßwasser reproduzierenden Neunaugen und Fische (Cyclostomata & Pisces). Naturschutz und Biologische Vielfalt 70: 291–316. [Google Scholar]
  • Freyhof J. Thymallus thymallus. The IUCN Red List of Threatened Species 2011:e.T21875A9333742, 2011, DOI: 10.2305/IUCN.UK.2008.RLTS.T21875A9333742.en. (accessed on: 2017/11/07). [Google Scholar]
  • Freyhof J, Brooks E. European Red List of Freshwater Fishes, Publications Office of the European Union, Luxembourg, 2011, http://ec.europa.eu/environment/nature/conservation/species/redlist/downloads/European_freshwater_fishes.pdf. (accessed on: 2017/11/03). [Google Scholar]
  • Gum B, Gross R, Kuehn R. 2005. Mitochondrial and nuclear DNA phylogeography of European grayling (Thymallus thymallus): evidence for secondary contact zones in central Europe. Mol Ecol 14: 1707–1725. [CrossRef] [PubMed] [Google Scholar]
  • Gum B, Gross R, Kuehn R. 2006. Discriminating the impact of recent human mediated stock transfer from historical gene flow on genetic structure of European grayling Thymallus thymallus L. J Fish Biol 69 (Suppl C): 115–135. [CrossRef] [Google Scholar]
  • Hanfland S, Laggerbauer B. Decline of graylings in Bavaria, their relation to cormorant population dynamics, and possibilities for recreational fishing, in: 6th World Recreational Fishing Conference − Toward Resilient Recreational Fisheries, Book of Abstracts, Berlin, Germany, 2011, pp. 100. [Google Scholar]
  • Hart PJ, Bergman E, Calles O, Eriksson S, Gustafsson S, Lans L, Norrgård J, Piccolo JJ, Rees N, Watz J, Österling M, Greenberg NA. 2014. Familiarity with a partner facilitates the movement of drift foraging juvenile grayling (Thymallus thymallus) into a new habitat area. Environ Biol Fish 5: 515–522. [CrossRef] [Google Scholar]
  • Havelka M. Genetic diversity of European grayling (Thymallus thymallus) and its relationship to the state of its populations in the Czech Republic, Master's Thesis, University of South Bohemia in České Budějovice, Faculty of Agriculture, 2009, 63 p. (in Czech). [Google Scholar]
  • Havelka M, Hucková D, Žurovcová M, Kohout J, Randák T, Flajšhans M. The impact of recent human mediated stock transfer on genetic structure of European grayling Thymallus thymallus L. in the Czech Republic, in: M. Pšenička, I. Němcová, Z. Dvořáková, K. Kovaříková, (Eds.), Diversification in Inland Finfish Aquaculture II (DIFA II), Vodňany, Czech Republic, 2013, pp. 80. [Google Scholar]
  • Heggberget TG, Johnsen BO, Hindar K, Jonsson B, Hansen LP, Hvidsten NA, Jensen AJ. 1993. Interactions between wild and cultured Atlantic salmon: a review of the Norwegian experience. Fish Res 18: 123–146. [CrossRef] [Google Scholar]
  • Johnsen BO, Hesthagen T. 1990. Recapture of pond- and hatchery-reared brown trout, Salmo trutta L., released in small streams. Aquacult Fish Manage 21: 245–252. [Google Scholar]
  • Jonsson S, Brännäs E, Lundqvist H. 1999. Stocking of brown trout, Salmo trutta L: effects of acclimatization. Fish Manage Ecol 6: 459–473. [CrossRef] [Google Scholar]
  • Kirchhöfer A, Breitenstein M, Zaugg B. Liste rouge poissons et cyclostomes-List rouge des espèces menacées en Suisse. Fédéral de l'environnement, Berne a Centre suisse de kartografie de la faune, Neuchâtel. L'environnement pratique 0734, 2007, pp. 64. [Google Scholar]
  • Lusk S, Hanel L, Lusková V. 2004. Red List of the ichthyofauna of the Czech Republic: Development and present status. Folia Zool 53: 215–226. [Google Scholar]
  • Magee L. 1993. A review of the grayling (Thymallus thymallus L.) in Yorkshire and some records of transfers of fish and ova. Naturalist 118: 115–122. [Google Scholar]
  • Meraner A, Unfer G, Gandolfi A. 2013. Good news for conservation: mitochondrial and microsatellite DNA data detect limited genetic signatures of inter-basin fish transfer in Thymallus thymallus (Salmonidae) from the Upper Drava River. Knowl Manage Aquat Ecosyst 409: 1. [CrossRef] [Google Scholar]
  • Northcote TG. 1995. Comparative biology and management of Arctic and European grayling (Salmonidae, Thymallus). Rev Fish Biol Fish 5: 141–194. [CrossRef] [Google Scholar]
  • Olla BL, Davis MW, Ryer CH. 1998. Understanding how the hatchery environment represses or promotes the development of behavioral survival skills. Bull Mar Sci 62: 531–550. [Google Scholar]
  • Olla BL, Davis MW, Ryer CH. 1994. Behavioural deficits in hatchery-reared fish: potential effects on survival following release. Aquacult Fish Manage 25 (Suppl. 1): 19–23. [Google Scholar]
  • Persat H, Mattersdorfer K, Charlat S, Schenekar T, Weiss S. 2016. Genetic integrity of the European grayling (Thymallus thymallus) populations within the Vienne River drainage basin after five decades of stockings. Cybium 40: 7–20. [Google Scholar]
  • Randák T. 2014. Fishery management in salmonid fishing grounds, in: T. Randák (Ed.), Fishery in Open Waters, University of South Bohemia in České Budějovice, Faculty of Fisheries and Protection of Waters, Vodňany, pp. 178–205. [Google Scholar]
  • Thorfve S. 2002. Impacts of in-stream acclimatization in post-stocking behaviour of European grayling in a Swedish stream. Fish Manage Ecol 9: 253–260. [Google Scholar]
  • Turek J, Horký P, Žlábek V, Velíšek J, Slavík O, Randák T. 2012. Recapture and condition of pond-reared, and hatchery-reared 1+ European grayling stocked in addition to wild conspecifics in a small river. Knowl Manage Aquat Ecosyst 5: 10. [CrossRef] [Google Scholar]
  • Uiblein F, Jagsch A, Honsig-Erlenburg W, Weiss S. 2001. Status, habitat use and vulnerability of the European T. thymallus in Austrian waters. J Fish Biol 59 (Suppl. A): 223–247. [Google Scholar]
  • UICN France, MNHN, SFI, ONEMA. La Liste rouge des espèces menacées en France − Chapitre Poissons d'eau douce de France métropolitaine, Paris, France, 2010. [Google Scholar]
  • Weiss SJ, Kopun T, Sušnik Bajec S. 2013. Assessing natural and disturbed population structure in European grayling Thymallus thymallus: melding phylogeographic, population genetic and jurisdictional perspectives for conservation planning. J Fish Biol 82: 505–521. [CrossRef] [PubMed] [Google Scholar]
  • Wolfram G, Mikschi E. Rote Liste der Fische (Pisces) Oesterreichs, in: K. Zulka (Ed.), Rote Liste gefaehrdeter Tiere Oesterreichs, Teil 2. Gruene Reihe des Lebensministerium Band 14/2, Boehlau-Verlag, Wien, Koeln, Weimar, 2007, pp. 61–198. [Google Scholar]

Cite this article as: Turek J, Žlábek V, Velíšek J, Lepič P, Červený D, Randák T. 2018. Influence of geographic origin on post-stocking survival and condition of European grayling (Thymallus thymallus) in a small river. Aquat. Living Resour. 31: 29

All Tables

Table 1

Number of grayling released at each site and tagging.

Table 2

Biometric data for tagged grayling before release: mean (±SD) standard length (LS), weight (W), and Fulton's condition factor (K).

Table 3

Biometric data for tagged grayling after recapture: mean (±SD) standard length (LS), weight (W), and Fulton's condition factor (K).

All Figures

thumbnail Fig. 1

Map showing the locations of release sites in the Blanice River. The inset shows location hatcheries producing the fish used in the survey.

In the text
thumbnail Fig. 2

Recapture rate (site fidelity = recapturing into release site/upstream = recapturing up of release site/downstream = recapturing down of release site) of stocked grayling in each site and total values (right column). *above bars indicates a significant difference (P < 0.05) in total recapture rate, different letters in bars indicate a significant difference (P < 0.05) in site fidelity/upstream/downstream recapture rate.

In the text

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.