Anguilla anguilla |
Present |
Present |
Hecht and Pienaar, 1993 |
Anguilla anguilla |
A RELIRE :!!! |
Absent |
Degani and Levanon, 1983 |
Aristichthys nobilis |
Cannibalism is observed in juveniles |
Present |
Kozlowski and Poczyczynski, 1999 |
Carassius auratus |
Cannibaslim by the parents on eggs and larvae ! |
Absent |
Horvath, 1992 |
Chondrostoma toxostoma |
No cannibalism or aggressive behaviour was observed |
Absent |
Gozlan, 1999 |
Ctenopharyngodon idella |
Cannibalism is observed in juveniles |
Present |
Kozlowski and Poczyczynski, 1999 |
Ctenopharyngodon idella |
No evidence of any form of aggression or cannibalism in silver carp, grasscarp |
Absent |
Hecht and Pienaar, 1993 |
Cyprinus carpio |
Cannibaslim during early life of enclosures |
Absent |
Dabrowski and Bardega, 1984 |
Cyprinus carpio |
Cannibalism as a possible cause of missing larvae (less than 7% in fed groups, less than 11% in unfed groups) was quite insufficient th explain the growth of living larvae |
Present |
Charlon and Bergot, 1984 |
Cyprinus carpio |
Sibling cannibaslim started in populations with a mean total length of c. 10.2 mm (on the 9th day after the start of exogeneous feeding) and with a cannibal to prey length ratio of 1.8 (12.9:7.2 mm). In all aquaria, cannibalism ceased when a mean total length of c. 35 mm was attained (after c. 55 days). Cannibalism was found to be positvely density-dependent |
Present |
Van Damme, 1989 |
Cyprinus carpio |
Cannibalism observed |
Present |
Bry, 1992 |
Cyprinus carpio |
Present |
Present |
Hecht and Pienaar, 1993 |
Cyprinus carpio |
Cannibalism is observed in juveniles |
Present |
Kozlowski and Poczyczynski, 1999 |
Cyprinus carpio |
Larval cannibalism was described in Koi carp, Cyprinus carpio |
Present |
Hatziathanasiou, 2002 |
Gobio gobio |
Not any cannibalism has ever been observed |
Absent |
Chemillier, 1995 |
Hypophthalmichthys molitrix |
No evidence of any form of aggression or cannibalism in silver carp, grasscarp |
Absent |
Hecht and Pienaar, 1993 |
Leucaspius delineatus |
With the onset of spawning period, adults may turn on feeding on their own eggs and larvae |
Absent |
Pipoyan, 1996 |
Leucaspius delineatus |
Throughout the spawing season, filial and hetero-cannibaslim was observed in all groups of individuals except parasitic males. Cannibalism in males guarding the nest site containing eggs was rare |
Present |
Gozlan, 2003 |
Phoxinus phoxinus |
Not described |
Absent |
Soin, 1982 |
Tinca tinca |
Unlike typical predatory fish such as northern pike Esox lucius that require, in order to avoid cannibalism, almost continuous intensive feeding throughout the rearing period, 24 h feeding or larval cyrpinids is generally not necessary |
Present |
Wolnicki,2003 |
Esox masquinongy |
If the grading extends over too long a period, cannibalism takes its toll of fish |
Present |
Sorenson, 1966 |
Esox masquinongy |
At that stage of development, the muskellunge were progressing from the larval to the juvenile period, and cannibalism was first detected |
Present |
Anonymous, 1982 |
Esox niger |
The species is cannibalistic under certain conditions |
Present |
Coffie, 1998 |
Esox niger |
NO INFORMATIONS |
Absent |
Armbruster, 1959 |
Esox lucius |
Cannibalism occured at the age of 3 weeks |
Present |
Wurtz, 1944 |
Esox lucius |
Within 2 weeks, cannibalism among the young pike became apparent |
Present |
Bryan, 1967 |
Esox lucius |
Cannibalism occured during the third weeks, at a size of 2.5 and below |
Present |
Chodorowski, 1975 |
Esox lucius |
Cannibalistic [This is the cannibalistic individuals that grow bigger and faster] |
Present |
Chodorowska and Chodorowski, 1975 |
Esox lucius |
Cannibalism is common in pike, may occur as early as 21 mm [Cannibalism intensity is highest where growth is omst heterogeneous] |
Present |
Bry and Gillet, 1980 |
Esox lucius |
At a size of 9 cm, it becomes cannibalistic, but could ocur earlier at 2.3 cm if insect populations are absent |
Absent |
Balvay, 1983 |
Esox lucius |
At 28-35 days cannibalism occured indepedently in all 12 tanks. The mean age at first cannibalism was 32 days (s.d. = 1.5 days) which occured at a mean length of 30.3 mm (s.d. 4.3 mm) |
Present |
Giles, 1986 |
Esox lucius |
"Cannibalism was observed from 21 days after the exogeneous feeding [mean total length 60 mm], most are ""Type II cannibalism"". May start at a total length of 21-23 mm" |
Present |
Bry, 1992 |
Esox lucius |
Present |
Present |
Hecht and Pienaar, 1993 |
Esox lucius |
The frequency of all cannibalistic attacks decreased in the order: highest>middle>lowest density |
Present |
Kucharczyk, 1997 |
Esox lucius |
Cannibalism occur when size is about 74 mm |
Present |
Bruslé and Quignard, 2001 |
Esox lucius |
Cannibalism was noticed on the 12th day of the experiment when pike larvae reached 16.0-22.3 mm SL (18.7 mm on average) |
Present |
Ziliukiene and Ziliukas, 2006 |
Lota lota |
Sibling intracohort cannibalism is present |
Present |
Kujawa, 2002 |
Lota lota |
No cannibalism occurred at any temperature throughout the experiment, although in this species it may appear at about 12 mm TL |
Absent |
Wolnicki, 2002 |
Gasterosteus aculeatus |
Male could eat some of their guarded eggs |
Absent |
Bruslé and Quignard, 2001 |
Gasterosteus aculeatus |
Lost of cannibalism |
Present |
Crivelli, 2001 |
Gasterosteus aculeatus |
Male eat egg and fry |
Absent |
Fitzgerald, 1983 |
Pungitius pungitius |
Male eat egg and fry |
Absent |
Fitzgerald, 1983 |
Micropterus dolomieui |
Present |
Present |
Chodorowski, 1975 |
Micropterus salmoides |
Apparently cannibalism had not decimated the new year classes in ponds stocked with bass alone |
Present |
Jonhson and McCrimmon, 1967 |
Micropterus salmoides |
Cannibalism occured among 24-mm fish, which reduced overall success rates |
Present |
Meyer, 1970 |
Micropterus salmoides |
Present |
Present |
Chodorowski, 1975 |
Micropterus salmoides |
Cannibalism can be a significant influence on young-of-the-year largemouth bass populations, especially when forage fish of suitable size are not available |
Present |
Deangelis, 1979 |
Micropterus salmoides |
Cannibalism described |
Present |
Bry, 1992 |
Micropterus salmoides |
Do cannibalims but not precised when ! |
Absent |
Bruslé and Quignard, 2001 |
Micropterus salmoides |
Cannibalism is frequent |
Present |
Carrel and Schlumberger, 2001 |
Micropterus salmoides |
During the indoor rearing, to reduce size variability and control cannibalism, it was necessary to submit fingerlings to frequent grading: the first at 150-200 mg, the second at 300 mg and third at 400 mg mean weight |
Present |
Roncarati, 2005 |
Dicentrarchus labrax |
NO INFORMATIONS |
Absent |
Barnabé, 1980 |
Dicentrarchus labrax |
Sea bass fingerlings, if not fed early in the morning, showed increased cannibalistic activities, 37% of the larger fish filled their stomachs with smaller siblings. The predator must be twice the length of the victim for ingestion. The extent of cannibalism is found to depend on feeding frequency |
Present |
Katavic, 1989 |
Dicentrarchus labrax |
Cannibalism described |
Present |
Bry, 1992 |
Dicentrarchus labrax |
Present |
Present |
Hecht and Pienaar, 1993 |
Dicentrarchus labrax |
Cannibalism was the main cause of death in post-larvae. Two types of cannibalism was detected: type I, attack from tail (observed at the beginning of the stage) and type II, attack from head (observed at the end of the stage) |
Present |
Hatziathanasiou, 2002 |
Morone saxatilis |
The growth differential among fry of the same age probably accounts for most cannibalistic activities starts about 2-3 weeks after hatching |
Present |
Braid, 1981 |
Morone saxatilis |
Cannibalism can be a serious problem in intensive culture of striped bass [could start when striped bass larvae were only 6 days |
Present |
Katavic, 1989 |
Morone saxatilis |
Cannibalism described |
Present |
Bry, 1992 |
Morone saxatilis |
Present |
Present |
Hecht and Pienaar, 1993 |
Perca flavescens |
Larvae are cannibalistic on their siblings [Cannibalism by adults also takes place weh nlarvae are > 18 mm] |
Present |
Craig, 2000 |
Perca flavescens |
The incidence of perch cannibalism was typically most intense in August when young perch averaged 40-70 mm length |
Present |
Tarby, 1974 |
Perca flavescens |
Yellow perch are known to be cannibaslitic |
Absent |
Kerr and Grant, 1999 |
Perca fluviatilis |
Present, at about 13 mm |
Present |
Goubier, 1990 |
Perca fluviatilis |
Cannibalism described |
Present |
Bry, 1992 |
Perca fluviatilis |
After one month, cannibalism occur in the mornings |
Present |
Wang and Eckmann, 1994 |
Perca fluviatilis |
Intense sibling cannibalism |
Present |
Kestemont, 1996 |
Perca fluviatilis |
The impact of cannibalism was proportionally decreased when fish grew more slowly |
Present |
Mélard, 1996 |
Perca fluviatilis |
One month after hatching, cannibalism occured in the mornings, before food was given |
Present |
Craig, 2000 |
Perca fluviatilis |
Perch can act as a piscivore from larval stage VI (body size 10.3 mm) on smaller siblings of its own cohort |
Absent |
Brabrand, 2001 |
Perca fluviatilis |
Is very frequent [Starts at abour 2.5 cm] |
Absent |
Dubois, 2001 |
Perca fluviatilis |
Data from the present study indicate that cannibalism emergence is not consistenstly size dependent in Eurasian perch larvae or young juveniles, and that re-establishment of this phenomenon at restocking is independent of the initial predator-prey relationship because size heterogeneity is negatively related to growth rate |
Present |
Mandiki, 2007 |
Sander lucioperca |
Cannibalism seems to be apply only to Central and Eastern European regions, not to Western Europe |
Present |
Deeler and Willemsen, 1964 |
Sander lucioperca |
In rearing conditions, cannibalism has been observed with individuals 2 to 4 cm long. In natural conditions, the cannibalism is maximal with individuals 1.1-2.0 cm long |
Present |
Chodorowski, 1975 |
Sander lucioperca |
Cannibalism could be a big problem |
Present |
Schlumberger and Proteau, 1993 |
Sander lucioperca |
This includes the onset of cannbalism due to the size differences bewteen indifviduals of this species. Bi-modality of size frequency distributions is a well-known phenomenon in this species. An earlier start of cannibaslim was observed in pike-perch of smaller size (less than 30 mm) fed in laboratory experiments using artifical diets, however cannibalism ceases at aout 5 cm body length (1.2 g). |
Present |
Hilge and Steffens, 1996 |
Sander lucioperca |
The first cannibalistic attacks were observed at 4-6th day after rearing |
Present |
Mamcarz, 1997 |
Sander lucioperca |
Larvae are cannibalistic on their siblings [Cannibalism by adults also takes place when larvae are > 18 mm] |
Present |
Craig, 2000 |
Sander lucioperca |
Mortality at all densities was mainly caused by cannibalism II type behaviour (27-35% of total). The first signs of cannibalism were observed in larvae measuring 15 mm in total length, and it increased after the larvae had exceeded 20 mm, consequently, it occurred primarily during the period when they fed exclusively on artificial feed |
Present |
Szkudlarek and Zakes, 2007 |
Sander vitreus |
Some cannibaslim was noted especially near the end of yolk absorption |
Absent |
Hurley, 1972 |
Sander vitreus |
Cannibalism is one of the most important source sof predation and in some situations amon fry, it may be the principal factor |
Present |
Colby, 1979 |
Sander vitreus |
Cannibalism among fry of other piscivorous fish species such as walleyes has greatly reduces production during intensive culture |
Present |
Braid, 1981 |
Sander vitreus |
"""Cohort cannibalism"" behavior dissapeared by the time larvae had reached about 16-19 mm" |
Present |
Li and Mathias, 1982 |
Sander vitreus |
The occurrence of cannibalism is reported from ages 6 to 16 days after hatching (120-214 DD). Population fry can be decimated unless steps are taken to control cannibalism |
Present |
Krise and Meade, 1986 |
Sander vitreus |
Cannibalism among other piscivorous fish species such as walleye can greattl reduce production during intensive culture in floating cages |
Present |
Katavic, 1989 |
Sander vitreus |
Cannibalism produced severe mortality |
Present |
Moodie, 1989 |
Sander vitreus |
"Cannibalism is frequent in predatory fishes, from ages 6 to 16, related to fish density [Mostly ""Type I ]cannibalism""" |
Present |
Bry, 1992 |
Sander vitreus |
Present |
Present |
Hecht and Pienaar, 1993 |
Sander vitreus |
Canibalism can occur in first-feeding fry |
Absent |
Colsesante, 1996 |
Sander vitreus |
Most mortality from cohort cannibaslim occurs from trunk attacks, not the result of successful consumption f the prey, which is from the tail first. Cannibalism begin as the fry begin feeding |
Present |
Summerfelt, 1996 |
Sander vitreus |
Larvae are cannibalistic on their siblings [Cannibalism by adults also takes place weh nlarvae are > 18 mm] |
Present |
Craig, 2000 |
Sander vitreus |
Walleye may turn cannibalistic at two stages during their early life stages. The first stage occurs within a week after hatching if zooplnakton is scarce in ponds, and the second stage develops about midsummer, when the young walleye are ready to feed on fish |
Present |
Kestemont and Mélard, 2000 |
Coregonus lavaretus |
Whitefish to a large extent cannibalize their own eggs |
Absent |
Skurdal, 1985 |
Coregonus lavaretus |
Never observed |
Absent |
Kozlowski and Poczyczynski, 1999 |
Coregonus lavaretus |
NO INFORMATIONS |
Absent |
Ylönen and Karjalainen, 2004 |
Coregonus albula |
Never observed |
Absent |
Kozlowski and Poczyczynski, 1999 |
Coregonus clupeaformis |
Never observed, no larval cannibalism was ever observed either in fish reared on artificial feed or on natural food |
Absent |
Kozlowski and Poczyczynski, 1999 |
Hucho hucho |
Cannibalism occured at fingerling stage in salmonid |
Present |
Kozlowski and Poczyczynski, 1999 |
Hucho hucho |
The year's cultivation is removed at the end of August or the beginning of september, since cannibalism considerably increases at this time, which can account for half the population in a month |
Present |
Penaz and Prihoda, 1981 |
Oncorhynchus mykiss |
Present |
Present |
Hecht and Pienaar, 1993 |
Oncorhynchus mykiss |
Newly hatched rainbow trout are sometimes cannibalized by juveniles of the same species |
Absent |
Kerr and Grant, 1999 |
Oncorhynchus mykiss |
The most numerous of the possible egg eaters seen around rainbow trout redds were juvenile of six to eight inches |
Absent |
Greeley, 1932 |
Salmo trutta fario |
It is probable that the smaller brown trout may be successful in picking up a few of the eggs of their own species |
Absent |
Greeley, 1932 |
Salvelinus alpinus |
It is not an uncommon occurrence that a young salmonid, having become cannibalistic, will take several days to fully ingest a captured sibling of similar dimensions |
Present |
Aasjord and Wallace, 1987 |
Salvelinus fontinalis |
Small, mature males were the most abundant of the egg eaters |
Absent |
Greeley, 1932 |
Thymallus arcticus |
Most of the grayling were eating fish eggs, but it was impossible to tell whether they were grayling of pike eggs |
Absent |
Bishop, 1971 |
Cottus gobio |
Male eat some eggs that they guard |
Absent |
Bruslé and Quignard, 2001 |
Cottus gobio |
The occurrence of egg cannibalism in guarding male varied throughout the season and reached a maximum of 80% in the sample of 12 March |
Present |
Marconato and Bisazza, 1988 |
Silurus glanis |
Fish loss to cannibalims was equal to 2% and 17 % of overall mortality in these groups respectively |
Absent |
Wolnicki, 1998 |
Silurus glanis |
In the course of the trial, the fish manifested neither sibling cannibalism nor any indications of an aggressive behavior |
Absent |
Wolnicki and Myszkowski, 1998 |
Silurus glanis |
Cannibalism was 7% lower in case of fish reared in darkness than in group [The level of cannibalism was directly related to stocking density in that experiment]. Cannibalism may be reduced by fish rearing in darkness, at stocking densities under 25 ind. dm-3 |
Present |
Kozlowski and Poczyczynski, 1999 |