Squalius cephalus (European chub)
- Summary of Invasiveness
- Taxonomic Tree
- Notes on Taxonomy and Nomenclature
- Distribution Table
- History of Introduction and Spread
- Risk of Introduction
- Habitat List
- Biology and Ecology
- Latitude/Altitude Ranges
- Notes on Natural Enemies
- Means of Movement and Dispersal
- Pathway Causes
- Pathway Vectors
- Impact Summary
- Environmental Impact
- Risk and Impact Factors
- Uses List
- Detection and Inspection
- Similarities to Other Species/Conditions
- Prevention and Control
- Links to Websites
- Distribution Maps
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PicturesTop of page
IdentityTop of page
Preferred Scientific Name
- Squalius cephalus (Linnaeus, 1758)
Preferred Common Name
- European chub
Other Scientific Names
- Cyprinus albula Nardo, 1827
- Cyprinus cephalus Linnaeus, 1758
- Cyprinus chub Bonnaterre, 1788
- Cyprinus kietaibeli Reisinger, 1830
- Cyprinus kittaibeli Reisinger, 1830
- Cyprinus lugdunensis Walbaum, 1792
- Cyprinus orthonotus Hermann, 1804
- Cyprinus rufus Vallot, 1837
- Cyprinus salmoneus Gronow, 1854
- Leucalburnus kosswigi Karaman, 1972
- Leuciscus albiensis Valenciennes, 1844
- Leuciscus albus (non Bonaparte, 1838)
- Leuciscus brutius Costa, 1838
- Leuciscus cabeda Risso, 1827
- Leuciscus cabeda pamvoticus (non Stephanidis, 1939)
- Leuciscus cavedanus Bonaparte, 1838
- Leuciscus cephaloides Battalgil, 1942
- Leuciscus cephalus (Linnaeus, 1758)
- Leuciscus cephalus albus Bonaparte, 1838
- Leuciscus cephalus cabeda Risso, 1827
- Leuciscus cephalus cephalus (Linnaeus, 1758)
- Leuciscus cephalus macedonicus Karaman, 1955
- Leuciscus cephalus moreoticus (non Stephanidis, 1971)
- Leuciscus cephalus orientalis Nordmann, 1840
- Leuciscus cephalus orientalis aralychensis Barach, 1934
- Leuciscus cephalus orientalis ardebilicus Barach, 1934
- Leuciscus cephalus orientalis kaznakovi Berg, 1912
- Leuciscus cephalus orientalis thracica Drensky, 1930
- Leuciscus cephalus orientalis thracicus Drensky, 1930
- Leuciscus cephalus orientalis zangicus Barach, 1934
- Leuciscus cephalus ruffoi Bianco & Recchia, 1983
- Leuciscus cephalus wjatkensis Lukasch, 1925
- Leuciscus chub pictava De la Pylaie, 1835
- Leuciscus cii (non Richardson, 1857)
- Leuciscus fellowesii Günther, 1868
- Leuciscus frigidus Valenciennes, 1844
- Leuciscus latifrons Nilsson, 1855
- Leuciscus nothulus Bonaparte, 1841
- Leuciscus orientalis Nordmann, 1840
- Leuciscus orientalis pursakensis Hanko, 1924
- Leuciscus peloponensis (non Valenciennes, 1844)
- Leuciscus rissoi Schinz, 1840
- Leuciscus ruffoi Bianco & Recchia, 1983
- Leuciscus squalius Valenciennes, 1844
- Leuciscus svallize zrmanjae risae Vladykov & Petit, 1930
- Squalius agdamicus (non Kamensky, 1901)
- Squalius berak Heckel, 1843
- Squalius cephaloides (Battalgil, 1942)
- Squalius cephalopsis Heckel, 1843
- Squalius cephalus (Linnaeus, 1758)
- Squalius cephalus athurensis Roule & Cardaillac de Saint-Paul, 1903
- Squalius cephalus cavedanus prespensis Karaman, 1924
- Squalius cephalus vardarensis (non Karaman, 1928)
- Squalius clathratus Blanchard, 1866
- Squalius meridionalis Blanchard, 1866
- Squalius meunier Heckel, 1852
- Squalius orientalis (non Heckel, 1847)
- Squalius orientalis (Nordmann, 1840)
- Squalius pareti Bonaparte, 1841
- Squalius turcicus (non De Filippi, 1865)
- Squalius turcicus platycephala Kamenskii, 1897
- Squalus tyberinus Bonaparte, 1841
International Common Names
- English: English chub; vardar chub
- Spanish: bagre
- French: cabot; chavasson; chevaine; chevesne; chovaine; juègne; meunier; mulet
- Russian: golavl; govali
Local Common Names
- Albania: blyshi; kleni; mëlyshi
- Austria: Döbel
- Belgium: kopvoorn; meun
- Bulgaria: rechen cefal; rechenclen
- Czech Republic: dyblink; jelec; klen; tloušt
- Denmark: almindelig døbel
- Finland: turpa
- Germany: Aitel; Aitel; Alsert; Breitschädel; Butt; Hässel
- Italy: cavedano
- Netherlands: Kopvoorn; meun
- Portugal: escalo
- Spain: bagra
- Sweden: färna
- Turkey: kepenez; talisu kefali
- UK: chub; round chub, fat chub, chevin, pollard
Summary of InvasivenessTop of page
The chub is a European freshwater cyprinid which has been reported as an invasive species in Italy and targeted for removal from a river system where introduced in Ireland. It is a long lived fish and has high mobility due to its pelagic condition. Humans may also facilitate its spread due to its value as a game or bait species in recreational fishing. It is also considered a valuable food resource in some regions, although the flesh is of poor quality (Dahl and Medem, 1964).
S. cephalus has ecological characteristics associated with invasiveness. It is omnivorous, and its food sources range from small (i.e. detritus, plants, invertebrates) to large (i.e. tadpoles, small fish) items. In addition it has high fecundity, fast growth rate, and is considered tolerant of anthropogenic pressures. However, there are few reports of impacts in its introduced range and indeed the changes in the taxonomic status of the species make it difficult to identify introduced populations.
Taxonomic TreeTop of page
- Domain: Eukaryota
- Kingdom: Metazoa
- Phylum: Chordata
- Subphylum: Vertebrata
- Class: Actinopterygii
- Order: Cypriniformes
- Family: Cyprinidae
- Genus: Squalius
- Species: Squalius cephalus
Notes on Taxonomy and NomenclatureTop of page
Squalius cephalus has long been considered to be widely distributed throughout most of Europe, from the Iberian Peninsula to the Urals, the Caspian Sea basin and central Iran. For a long time, many Squalius populations in the Mediterranean basin have attracted little attention and they have been uncritically identified as S. cephalus or dumped into a “S. cephalus complex” or “S. cephalus species group”.
Several peri-Mediterranean populations are now considered morphologically and genetically distinct enough to be considered valid species or subspecies. Some morphological characters may be difficult to identify in live fish and, in particular, in juveniles: therefore, genetic analysis is recommended for correct identification. The recent description of new species and the previous wide range of S. cephalus makes the identification of introduced populations in Europe difficult.
DescriptionTop of page
The chub (S. cephalus) is a freshwater fish species (Cyprinidae family) that inhabits slow and moderate water flows from a wide range of European waters. It has 3 dorsal spines in total, 7-9 dorsal soft rays, 3 anal spines, 7-10 anal soft rays and 42-48 vertebrae. The mean size is 30.0 cm TL male/unsexed (Muus and Dahlström, 1968) and the maximum length reported is 60.0 cm SL male/unsexed (Kottelat and Freyhof, 2007). The maximum age reported is 22 years (Wüstemann, 1995). The maximum published weight is 8.0 kg (Spillman, 1961).
DistributionTop of page
Froese and Pauly (2011) describe the distribution as Eurasia: North, Baltic, northern Black, White, Barents and Caspian Sea basins, Atlantic basins southward to Adour drainages (France), Great Britain north to 56°N. Scandinavia: southern Finland, Sweden north to about Stockholm. Mediterranean basin from Var to Hérault (possibly Aude) (France) drainages. Naturally absent from Italy and the Adriatic basin.
Distribution TableTop of page
The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.Last updated: 10 Jan 2020
|Continent/Country/Region||Distribution||Last Reported||Origin||First Reported||Invasive||Reference||Notes|
|Armenia||Present||Native||Blanc et al. (1971)||Recorded from almost all reservoirs in Armenia|
|Azerbaijan||Present||Native||Blanc et al. (1971)|
|Georgia||Present||Native||Blanc et al. (1971)|
|Iran||Present||Native||Bogutskaya (1997)||Recorded in Caspian Sea, Lake Urmia, Namak Lake and Tigris River basins. Also found in Qom River, inner drainage from northern Iran|
|Kazakhstan||Present||Native||Blanc et al. (1971)|
|Turkey||Present||Native||Bogutskaya (1997)||Known from the Gümüldür stream near Izmir. A short-lived species which inhabits water courses in lowland rivers. Is threatened due to habitat destruction and pollution|
|Austria||Present||Native||Blanc et al. (1971)||Status of threat: Least concern|
|Belarus||Present||Native||Blanc et al. (1971)|
|Belgium||Present||Native||Blanc et al. (1971)|
|Bosnia and Herzegovina||Present||Native||Gerstmeier and Romig (1998)|
|Bulgaria||Present||Native||Blanc et al. (1971)|
|Croatia||Present||Native||Gerstmeier and Romig (1998)|
|Czechia||Present||Native||Gerstmeier and Romig (1998)||Occurs in Odra and Morava river basins. Status of threat: Least concern|
|Estonia||Present||Native||CABI (Undated)||Rare in the Gulf of Riga and Gulf of Finland; Original citation: Anon (1999)|
|Finland||Present, Widespread||Native||Koli (1990)||Occurs on the coast of the Gulf of Finland, and up to the River Kokemäenjoki mouth on the coast of the Gulf of Bothnia, and in many rivers flowing towards South and Southeast coasts|
|France||Present||Native||Keith and Allardi (2001)||Found in the metropolitan territory. Not reported in Finistère, Corse, Nord and Landes. A different form with a smaller head is encountered in the south of France. Adults occur in creeks and fast flowing rivers, occasionally in lakes|
|Germany||Present, Few occurrences||Native||Spratte and Hartmann (1997)||Potentially threatened in Schleswig-Holstein in 1990|
|Greece||Present||Native||Blanc et al. (1971)||Known from Prespa lakes. Also recorded from the Strymonikos Gulf|
|Hungary||Present||Native||Blanc et al. (1971)|
|Ireland||Present||2010||Introduced||Caffrey et al. (2008)||Introduced to River Inny in the late 1990s early 2000s by anglers. Capture campaign began in 2006.|
|Italy||Present||Introduced||Invasive||Kottelat and Freyhof (2007)||Has been stocked in rivers and recorded as invasive. Recorded from Ombrone, Albegna, Fiora and Bruna|
|Latvia||Present||Native||Blanc et al. (1971)|
|Lithuania||Present, Widespread||Native||Blanc et al. (1971)|
|Moldova||Present||Native||Blanc et al. (1971)|
|Netherlands||Present, Few occurrences||Native||Blanc et al. (1971)|
|Norway||Present||Native||Blanc et al. (1971)|
|Poland||Present, Few occurrences||Native||Muus and Dahlström (1968)||Important food fish in early-mediaeval times|
|Russia||Present||Native||Reshetnikov et al. (1997)||Occurs in the basins of the Baltic and White Seas (up to the Northern Dvina), in river basins of the Sea of Azov, Black and Caspian Sea (up to the Ural River in the east)|
|Serbia||Present||Native||Blanc et al. (1971)||In Serbia, Montenegro and Kosovo|
|Slovakia||Present||Native||Gerstmeier and Romig (1998)|
|Slovenia||Present||Native||Gerstmeier and Romig (1998)|
|Spain||Present||Native||Elvira (1996)||Threatened due to habitat destruction, pollution, and introductions of exotic predators. Status of threat: vulnerable. Species has been subject to commercial fishing|
|Sweden||Present||Native||Kottelat and Freyhof (2007)||Occurrence: Native and regular|
|Switzerland||Present||Native||Muus and Dahlström (1968)||In Lakes, rivers and creeks, close to the shore. Fairly common|
|United Kingdom||Present||Native||Maitland and Campbell (1992)||Native to UK but introduced to Loch Lomond|
|Atlantic - Northeast||Present||Native||Froese and Pauly (2011)|
|Indian Ocean - Eastern||Present||Native||Froese and Pauly (2011)|
|Indian Ocean - Western||Present||Native||Froese and Pauly (2011)|
|Mediterranean and Black Sea||Present||Native||Froese and Pauly (2011)|
History of Introduction and SpreadTop of page
A few chub were found in the River Inny, Ireland, and are presumed to have been introduced intentionally by anglers in the late 1990s or early 2000s to improve the diversity of coarse angling species available. While relatively few were captured during a survey in 2006 (17 individuals), those examined were healthy and most were in spawning condition (Caffrey et al., 2008) and an eradication campaign was initiated. Bartley (2006) reported the introduction of Leuciscus cephalus [S. cephalus] to Italy but its origin was not determined. Other possible introductions of this fish species have not yet been reported: recent description of new species and previous wide range makes identification of introduced populations difficult (see Notes on Taxonomy and Nomenclature).
IntroductionsTop of page
Risk of IntroductionTop of page
The chub is not of interest to the aquarium trade, but is considered a valuable food resource in some countries and also has interest as a game or bait fish species. Therefore, recreational fishing and interconnection of waterways represent the main pathways of introduction into new locations.
HabitatTop of page
S. cephalus inhabits pools and tables from small to large rivers, and there are also populations described in lakes or reservoirs. Lake populations migrate to inflowing streams for spawning that preferably takes place in fast-flowing waters with gravel bottoms, rarely among submerged vegetation (Kottelat and Freyhof, 2007).
Adults are usually solitary or occur in small swarms, whereas juveniles form large swarms. Adults are usually found in pools, whereas juveniles live in very shallow shoreline habitats (Kottelat and Freyhof, 2007).
Habitat ListTop of page
|Irrigation channels||Secondary/tolerated habitat||Natural|
|Rivers / streams||Principal habitat||Natural|
Biology and EcologyTop of page
Some genetic records were listed with the same values in the River Kupa, South Pyrenees, Yugoslavia and other unspecified localities. Haploid/gametic chromosome number (n) is 25, whereas diploid/Zygotic chromosome number (2n) is 50-50 (Al-Sabti, 1986; Klinkhardt et al., 1995; Arkhipchuk, 1999).
Sokolov and Berdicheskii (1989) reported that spawning occurs in fast-flowing water above gravel bottom, rarely among submerged vegetation. Males reach sexual maturity at the age of 2-4 years whereas females reach it at 4-6. Maturity is influenced by environmental factors and some individuals may mature much later. Spawning takes place in May-August, when temperature rises above 14ºC. Multiple spawning is described during each breeding season. Males assemble at spawning sites and follow ripe females, often with much splashing, to shallow riffles. Females then lay sticky eggs into the gravel (Kottelat and Freyhof, 2007). Pale yellow eggs are found attached to gravel, weed and stones in flowing water (Pinder, 2001). Billard (1997) also reported eggs added to plants.
Fecundity varies seasonally and geographically. The lowest value of fecundity (1158-2050 eggs) was detected in Turkey (Ünver, 1998; Ünlü and Balci, 1993) and the highest values (100,000 eggs) were detected in Europe (Vostradovsky, 1973). Maitland and Campbell. (1992) reported the same maximum values in Western Greece and Peloponnese.
Physiology and Phenology
Tolerant of anthropogenic impacts. Further studies are required.
S. cephalus lives up to 15 years, females longer than males (Kottelat and Freyhof, 2007). Maximum reported age is 22 years (Wüstemann, 1995)
Population Size and Density
Abundant. Unknown population trend.
Feeds on a wide variety of aquatic and terrestrial animals and plant material. Large individuals are predominantly piscivorous (Kottelat and Freyhof, 2007). In the UK is recorded as feeding on worms, molluscs, crustaceans, and various insect larvae (Maitland and Campbell, 1992); large chub eat considerable numbers of small fish, such as chub, eels, dace, roach, gudgeon and minnows; also frogs, crayfish, voles and young water birds. Further information on natural food sources is as follows:
Natural Food Sources
Contribution to total food intake (%)
Plants, benthic algae, weeds
42.9% (28.3% algae, 14.6% macrophytes)
Nekton, fish juveniles (Anguilla anguilla, Gobio gobio, Leuciscus leuciscus, Phoxinus phoxinus, Rutilus rutilus)
28.3% (18.3% eel, 2.7% minnow, 1.8% bullhead, 1.3% grayling, 0.1% stickleback, 4.3% unid. fish)
11.8% (7% Caddis larvae, 0.4 % blackfly larvae and pupae, 0.2% stonefly larvae, 0.1% mayfly larvae, 0.1% mayfly larvae, 0.1% midge larvae)
Zooplankton (crayfish), plankton, crustaceans
3% (2.5% terrestrial organisms, 0.5% water vole)
Herpetofauna, toads, frogs
Other benthonic invertebrates
S. cephalus prefers slow-flowing waters. Although it is considered tolerant to anthropogenic perturbations, large animals may be particularly vulnerable to reduced water flow levels due to the pelagic conditions of the species. Detailed studies on environmental preferences to establish lower and upper tolerance values have not been published. A study performed on Iberian populations of S. laietanus (i.e. formerly S. cephalus) considers the species tolerant to poor water quality and physical habitat degradation gradients (Maceda-Veiga and De Sostoa, 2011).
Latitude/Altitude RangesTop of page
|Latitude North (°N)||Latitude South (°S)||Altitude Lower (m)||Altitude Upper (m)|
Notes on Natural EnemiesTop of page
All piscivorous species are the chub’s natural enemies (e.g. birds, mammals, introduced and native piscivorous fish species).
Means of Movement and DispersalTop of page
S. cephalus is a potamodromous species. Migrations take place during the breeding season. It can cover more than 100 km (Riede, 2004). The latitude and longitude migration movements range from 10°W to 60°E and 64°N to 35°N, respectively.
Pathway CausesTop of page
Pathway VectorsTop of page
Impact SummaryTop of page
Environmental ImpactTop of page
The introduction of exotic species may cause hybridization with native species, predation, resource competition and agonistic behaviour with native species and/or the introduction of diseases. Chub does not represent a risk for humans but it may cause changes to ecosystems (i.e. altering food web structures) and it may predate on native species. The risk of hybridization is particularly important with closely related fish species, in particular with other members of the Squalius genus. Fertile hybrids with Alburnus alburnus have also been reported (Kottelat and Freyhof, 2007). Studies on the effects of chub on native fish species are lacking.
Risk and Impact FactorsTop of page Impact outcomes
- Altered trophic level
- Ecosystem change/ habitat alteration
- Modification of natural benthic communities
- Highly likely to be transported internationally deliberately
- Highly likely to be transported internationally illegally
- Difficult to identify/detect in the field
- Difficult/costly to control
UsesTop of page
The chub is of no interest to the aquarium trade, but is considered a valuable food resource in some countries despite poor quality of the flesh. It also has interest as a game or bait fish species in recreational fishing.
Uses ListTop of page
Animal feed, fodder, forage
- Sport (hunting, shooting, fishing, racing)
DiagnosisTop of page
The similar morphological traits between species of the Squalius genus require the aid of specialists to distinguish between them. The combination of morphological and genetic traits may also be necessary to ensure proper identification (particularly in juvenile specimens) and this procedure may also allow detection of hybrids.
Detection and InspectionTop of page
The existence of stowaway species mixed with valuable species in ornamental or any other live fish stocks is not uncommon. The live fish trade therefore requires careful inspection by specialists in order to detect undesirable organisms which are often not labeled. In addition, the regular monitoring of current waters allows managers to detect new fish introductions and to know the spread patterns of exotic species once introduced. This information helps resource managers to identify areas at high risk of invasion and to plan local eradication programs when possible. Electrofishing is a widely recognized method to catch fish without damaging the ecosystem. Nets are a complementary sampling tool for surveys performed in lakes or reservoirs.
Similarities to Other Species/ConditionsTop of page
Differs from its congeners in France, North, Baltic, Arctic, Black and Caspian Sea basins by possession of the following characteristics: dorsal profile with a well-marked discontinuity between head and trunk; a row of black pigments along free margin of each flank scale, forming a regular reticulate pattern, with no or very few pigments on central part of scales; anal and pelvic fins orange to red; dorsal fin with 8½ branched rays; anal fin with 8½ branched rays (rarely 9½); scales on lateral line 40-45 + 2-3; mouth terminal, with well-marked chin; lower jaw tip not included in the upper lip; interorbital distance 37-42% HL; postorbital distance 47-51% HL; eye diameter 17-22% HL, 1.5-2.3 times in snout length; body depth 22-27% SL; lower jaw long, length greater than depth of operculum; iris whitish; pharyngeal teeth 2,5-5,2; in stretched anal fin of individuals larger than about 15 cm SL, distance between tips of first and last branched rays usually greater than caudal peduncle depth. Size up to at least 600 mm SL (Kottelat and Freyhof, 2007). Caudal fin with 19 rays (Spillman, 1961).
Prevention and ControlTop of page
Due to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.
Education programmes can be used to raise public awareness about the threats of introduced species to ecosystems. Regular monitoring of waters by trained specialists can be used to detect new invaders and newly invaded areas.
Once established, complete eradication is almost impossible, particularly in large areas. Local extirpation of introduced fish species may be performed in areas of high conservation value, particularly in small streams where the probability of success increases. In the River Inny, Ireland, a netting and electrofishing campaign has been running since 2006 to control a small number of introduced chub (Caffrey et al., 2008) with the result that none have been detected since 2010 (J Caffrey, Inland Fisheries Ireland, personal communication, 2012).
Physical barriers and rotenone are commonly used to control small fish. Regular removal of specimens in small streams may mitigate the effect of exotic species.
Monitoring and Surveillance
Regular electrofishing surveys.
ReferencesTop of page
Al-Sabti K, 1986. Karyotypes of Cyprinus carpio and Leuciscus cephalus. Cytobios, 47(188):19-25.
Anon., 1999. Systematic list of Estonian fishes. World Wide Web Electronic Publication, 14 January 2000. http://bio.edu.ee/animals/Kalad/kalalist2.htm
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Billard R, 1997. Les poissons d’eau douce des rivieres de France. Identification, inventaire et repartition des 83 especes. Lausanne: Delachaux and Niestle, 192 pp.
Blanc M; Gaudet JL; Banarescu P; Hureau JC, 1971. European inland water fish: a multilingual catalogue. London: Fishing News (Books) Ltd.
Bogutskaya NG, 1997. Contribution to the knowledge of leuciscine fishes of Asia Minor. An annotated checklist of leuciscine fishes (Leuciscinae, Cyprinidae) of Turkey with descriptions of a new species and two new subspecies. Mitt. Hamb. Zool. Mus. Inst. 94:161-186.
Caffrey JM; Acevedo S; Gallagher K; Britton R, 2008. Chub (Leuciscus cephalus): a new potentially invasive fish species in Ireland. Aquatic Invasions, 3(2):201-209. http://www.aquaticinvasions.ru/2008/AI_2008_3_2_Caffrey_etal.pdf
Dahl G; Medem F, 1964. [English title not available]. (Informe sobre la fauna acuatica del río Sinú.) Informe sobre la fauna acuatica del río Sinú. Bogata, Colombia: Corporacion Autonoma Regional de los Valles del Magdalena y del Sinu-CVM-Depto. de Investigaciones Ictiologicas y Faunisticas, Bogotá, 109 pp.
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Gerstmeier R; Romig T, 1998. Die Süßwasserfische Europas: für Naturfreunde und Angler. Stuttgart, Germany: Franckh-Kosmos Verlag, 368 pp.
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Reshetnikov YS; Bogutskaya NG; Vasil'eva ED; Dorofeeva EA; Naseka AM; Popova OA; Savvaitova KA; Sideleva VG; Sokolov LI, 1997. An annotated check-list of the freshwater fishes of Russia. J. Ichthyol, 37(9):687-736.
Riede K, 2004. Global register of migratory species - from global to regional scales. Final Report of the R&D-Projekt 808 05 081. Bonn, Germany: Federal Agency for Nature Conservation, 329 pp.
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Vostradovsky J, 1973. Freshwater fishes. London, UK: The Hamlyn Publishing Group Limited, 252 pp.
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Ünlü E; Balci K, 1993. Observation on the reproduction of Leuciscus cephalus orientalis (Cyprinidae) in Savur stream (Turkey). Cybium, 17(3):241-250.
Ünver B, 1998. An Investigation on the Reproduction Properties of Chub Leuciscus cephalus (L.,1758) in Lake Tödürge (Zara/Sivas). Turkish Journal of Zoology, 22:141-147.
Bogutskaya N G, 1997. Contribution to the knowledge of leuciscine fishes of Asia Minor, Part 2. An annotated checklist of leuciscine fishes (Leuciscinae, Cyprinidae) of Turkey with descriptions of a new species and two new subspecies. Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut. 161-186.
CABI, Undated. Compendium record. Wallingford, UK: CABI
Caffrey J M, Acevedo S, Gallagher K, Britton R, 2008. Chub (Leuciscus cephalus): a new potentially invasive fish species in Ireland. Aquatic Invasions. 3 (2), 201-209. http://www.aquaticinvasions.ru/2008/AI_2008_3_2_Caffrey_etal.pdf DOI:10.3391/ai.2008.3.2.11
Dhora D, 2010. Register of Species of the Fauna of Albania 2010. (Regjistër I specieve të faunës së Shqipërisë 2010). In: Register of Species of the Fauna of Albania 2010, Shkodër, Shkodër: Camaj-Pipa.
Elvira B, 1996. Endangered freshwater fish of Spain. In: Conservation of Endangered Freshwater Fish in Europe, [ed. by Kirchhofer A, Hefti D]. Basel, Switzerland: Birkhäuser Verlag. 55-61.
Gerstmeier R, Romig T, 1998. (Die Süßwasserfische Europas: für Naturfreunde und Angler)., Stuttgart, Germany: Franckh-Kosmos Verlag. 368 pp.
Reshetnikov Y S, Bogutskaya N G, Vasil'eva E D, Dorofeeva E A, Naseka A M, Popova O A, Savvaitova K A, Sideleva V G, Sokolov L I, 1997. An annotated check-list of the freshwater fishes of Russia. J. Ichthyol. 37 (9), 687-736.
Spratte S, Hartmann U, 1997. [English title not available]. (Fischartenkataster: Süsswasserfische und Neunaugen in Schleswig-Holstein. Ministerium für ländliche Räume, Landwirtschaft, Ernährung und Tourismus, Kiel Germany)., [ed. by Froese R, Pauly D]. FishBase. World Wide Web electronic publication. http://www.fishbase.org
OrganizationsTop of page
Italy: FAO (Food and Agriculture Organization of the United Nations), Viale delle Terme di Caracalla, 00100 Rome, http://www.fao.org/
ContributorsTop of page
04/01/12 Original text by:
Mònica Utjés Mascó, Department of Animal Biology & Research Institute of Biodiversity (IrBio), Faculty of Biology, University of Barcelona, Avda Diagonal, 643. E-08028 Barcelona, Spain
Alberto Maceda Veiga, Department of Animal Biology & Research Institute of Biodiversity (IrBio), Faculty of Biology, University of Barcelona, Avda Diagonal, 643. E-08028 Barcelona, Spain
The names of reviewers are available from CABI on request.
Distribution MapsTop of page
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