Trait completeness | 94% |
Total data | 201 |
References | 39 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 6.4-6.6 | 6.5 mm | Hovarth et al, 1992 |
8 | Initial larval size | 7.0 | 7.0 mm | Mittelbach and Persson, 1998 |
8 | Initial larval size | 6.4-6.6 | 6.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | By DPH 3 : average TL is 7.4 ± 0.894 mm ranging from 6 to 8 mm | 7.4 mm | Kozaric et al, 2008 |
9 | Larvae behaviour | To start with the yellow and helpless larvae lay at the bottom of the boxes. On the 2nd and 3rd day, as they became greyish, they gathered in the darker corner | Demersal | Horvath, 1977 |
9 | Larvae behaviour | Remains fixed to roots of the nest by a ceplalic cement glands | Demersal | Bruslé and Quignard, 2001 |
9 | Larvae behaviour | Remain motionless on the bottom, 5-6 days after they swim well | Demersal | Linhart et al, 2002 |
10 | Reaction to light | Light caused aggressive bahavior of fish, they crowded at the bottom, near the walls, and in tank corers. The fish reared in darkness were evenly dispersed in the entire water volume and did not crowd | Photopositive | Kozlowski and Poczyczynski, 1999 |
10 | Reaction to light | Photophobic | Photophobic | Bruslé and Quignard, 2001 |
11 | Temperature during larval development | 22-26 | 24.0 °C | Horvath, 1977 |
11 | Temperature during larval development | 25-30 | 27.5 °C | Wolnicki et al, 1998 |
11 | Temperature during larval development | 26-28 | 27.0 °C | Kozlowski and Poczyczynski, 1999 |
11 | Temperature during larval development | 22-25 for the first 2-3 days, 25-28 for the other 2-3 days | 23.5 °C | Linhart et al, 2002 |
11 | Temperature during larval development | Both systems were supplied with the same treated wter from a water-pipe network with temperature ranging from 23 to 26°C | 23.0 °C | Brzuska and Adamek, 1999 |
12 | Sibling intracohort cannibalism | Fish loss to cannibalims was equal to 2% and 17 % of overall mortality in these groups respectively | Absent | Wolnicki et al, 1998 |
12 | Sibling intracohort cannibalism | In the course of the trial , the fish manifested neither sibling cannibalism nor any indications of an aggressive behavior | Absent | Wolnicki and Myszkowski, 1998 |
12 | Sibling intracohort cannibalism | 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 |
13 | Full yolk-sac resorption | A yolk sac was present during the first 5 days (1-5 DPH) | 3.0 °C * day | Kozaric et al, 2008 |
14 | Onset of exogeneous feeding | After their first feeding (5-7 days old) at temperature of 22-26°C | 6.0 °C * day | Horvath, 1977 |
14 | Onset of exogeneous feeding | 125 [5 days at 25°C] | 125.0 °C * day | Wolnicki et al, 1998 |
14 | Onset of exogeneous feeding | 130 [5 days at 28°C] | 130.0 °C * day | Wolnicki and Myszkowski, 1998 |
14 | Onset of exogeneous feeding | 150.0 | 150.0 °C * day | Linhart et al, 2002 |
14 | Onset of exogeneous feeding | Exogenous feeding started at DPH 4 and there was a 2-day mixed endogenous-exogenous feeding period | 4.0 °C * day | Kozaric et al, 2008 |
10 | Reaction to light | Photonegative | Photophobic | Copp et al, 2009 |
8 | Initial larval size | 5-6 | 5.5 mm | Proteau et al, 2008 |
10 | Reaction to light | photonegative. "groupées en zone sombre" | Photophobic | Proteau et al, 2008 |
12 | Sibling intracohort cannibalism | yes | Present | Guillaume, 2012 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4 [Mass maturation in 5-6 years] | 5.5 year | Zholdasova and Guseva, 1987 |
15 | Age at sexual maturity | Mass maturation occurs in the 3-4 th year of life. However the maturation rate may be accelerated to 2 year [Sex not specified] | 3.5 year | Orlova, 1987 |
15 | Age at sexual maturity | 4-5 | 4.5 year | Hovarth et al, 1992 |
15 | Age at sexual maturity | 4-5 | 4.5 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3-5 [Sex not specified] | 4.0 year | Schlumberger and Proteau, 2001 |
15 | Age at sexual maturity | The smallest mature female was 4 years old [3-4 for females in other sutides] | 3.5 year | Alp et al, 2004 |
15 | Age at sexual maturity | 3-4 | 3.5 year | Fishbase, 2006 |
16 | Length at sexual maturity | Mass maturation occurs at 57-66 cm, however the maturation rate may be 50.7 [Sex not specified] | 61.5 cm | Orlova, 1987 |
16 | Length at sexual maturity | 63.5 | 63.5 cm | Zholdasova and Guseva, 1987 |
16 | Length at sexual maturity | 50-70 | 60.0 cm | Hovarth et al, 1992 |
16 | Length at sexual maturity | 50-60 [Sex not specified] | 55.0 cm | Schlumberger and Proteau, 2001 |
16 | Length at sexual maturity | The smallest mature female was 86.0 cm [85.0-90.0 cm], also [58-60 for both sex in other studies] | 87.5 cm | Alp et al, 2004 |
17 | Weight at sexual maturity | Mass maturation occurs at 1.3-2.3 kg, however the maturation rate may be 1.22 kg [Sex not specified] | 1.8 kg | Orlova, 1987 |
17 | Weight at sexual maturity | 2.6 | 2.6 kg | Zholdasova and Guseva, 1987 |
17 | Weight at sexual maturity | 4-12 | 8.0 kg | Hovarth et al, 1992 |
17 | Weight at sexual maturity | 2 [Sex not specified] | 2.0 kg | Schlumberger and Proteau, 2001 |
17 | Weight at sexual maturity | The smallest mature female was 4.434 [1-2, 1.43 for both sex in other studies] | 1.5 kg | Alp et al, 2004 |
19 | Relative fecundity | About 30 [A female of 2 kg release 60000 eggs] | 30.0 thousand eggs/kg | Maitland, 1977 |
19 | Relative fecundity | 10-48 | 29.0 thousand eggs/kg | Hovarth et al, 1992 |
19 | Relative fecundity | 10-25 [Usual fecundity of female broodfish] | 17.5 thousand eggs/kg | Legendre et al, 1997 |
19 | Relative fecundity | 7-42 | 24.5 thousand eggs/kg | Mittelbach and Persson, 1998 |
19 | Relative fecundity | 20-30 | 25.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 20-30 | 25.0 thousand eggs/kg | Schlumberger and Proteau, 2001 |
19 | Relative fecundity | 8.443 +/ 1.114 [12,7 in other studies] | 8.44 thousand eggs/kg | Alp et al, 2004 |
20 | Absolute fecundity | Number of the yellow oocytes in particular females amounted to from 34.7 thousand in a female weghting 5.3 kg to 788.0 thousand in a female weighting 36.0 kg [Described in other study : 38592-306240; 11810-1380000; 27400-384500; 42822-391411; 356400; 14600-285000; 61400-249300] | 172416.0 thousand eggs | Wisniewolski, 1988 |
20 | Absolute fecundity | 50-200 | 125.0 thousand eggs | Hovarth et al, 1992 |
20 | Absolute fecundity | Mean fecundity 87,108 +/ 20,992 [Range 9,033 to 340,461 for females ranging from 86.0 to 151.0 cm] | 87.0 thousand eggs | Alp et al, 2004 |
21 | Oocyte development | Asynchronous development of sex cells | Asynchronous | Zholdasova and Guseva, 1987 |
21 | Oocyte development | Two groups of the oocytes were present in all samples [Also described as: asynchronic development of the oocytes was observed in catfish as late as 10 days before spawning] | Asynchronous | Wisniewolski, 1988 |
22 | Onset of oogenesis | Yolk accumulation in the oocytes of the old generation begins in autumn, and continues for 7-8 months | ['October', 'November', 'December'] | Zholdasova and Guseva, 1987 |
22 | Onset of oogenesis | The peak of vitellogenesis was observed in summer (July-August), and females passed winter with the ovaries in the IV th stage of development | ['January', 'February', 'March', 'July', 'August', 'September'] | Wisniewolski, 1988 |
23 | Intensifying oogenesis activity | Supplementary vitellogenesis took place in spring | ['April', 'May', 'June'] | Wisniewolski, 1988 |
24 | Maximum GSI value | 7.5% [Maturation coefficient, measured prior to spawning] | 7.5 percent | Zholdasova and Guseva, 1987 |
24 | Maximum GSI value | 3-15 [GSI usually found in female broodstock] | 9.0 percent | Legendre et al, 1997 |
24 | Maximum GSI value | 4.5% [May] | 4.5 percent | Alp et al, 2004 |
25 | Oogenesis duration | 7-8 months | 7.5 months | Zholdasova and Guseva, 1987 |
25 | Oogenesis duration | From December to May | 7.0 months | Alp et al, 2004 |
26 | Resting period | July, August: 0.42-0.81% | 3.0 months | Zholdasova and Guseva, 1987 |
26 | Resting period | September-October: >0.05% | 3.0 months | Alp et al, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3 [Mass maturation at 4-5] | 4.5 years | Zholdasova and Guseva, 1987 |
27 | Age at sexual maturity | Mas maturation occurs in the 3-4 th year of life. However the maturation rate may be accelerated to 2 year [Sex not specified] | 3.5 years | Orlova, 1987 |
27 | Age at sexual maturity | 3-4 | 3.5 years | Hovarth et al, 1992 |
27 | Age at sexual maturity | 3-5 [Sex not specified] | 4.0 years | Schlumberger and Proteau, 2001 |
27 | Age at sexual maturity | 3-4 | 3.5 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | Smallest males belonged at 3 years old [2-3 in other studies] | 2.5 years | Alp et al, 2004 |
27 | Age at sexual maturity | 2-3 [Male] | 2.5 years | Fishbase, 2006 |
28 | Length at sexual maturity | Mass maturation occurs at 57-66 cm, however the maturation rate may be 50.7 [Sex not specified] | 61.5 cm | Orlova, 1987 |
28 | Length at sexual maturity | 70.5 | 70.5 cm | Zholdasova and Guseva, 1987 |
28 | Length at sexual maturity | 50-70 | 60.0 cm | Hovarth et al, 1992 |
28 | Length at sexual maturity | 50-60 [Sex not specified] | 55.0 cm | Schlumberger and Proteau, 2001 |
28 | Length at sexual maturity | Smallest males belonged to the 80-85 cm length class [the smallest male was 83.0 cm], also [58-60 both sex, other studies] | 82.5 cm | Alp et al, 2004 |
29 | Weight at sexual maturity | Mass maturation occurs at 1.3-2.3 kg, however the maturation rate may be 1.22 kg [Sex not specified] | 1.8 kg | Orlova, 1987 |
29 | Weight at sexual maturity | 2.2 | 2.2 kg | Zholdasova and Guseva, 1987 |
29 | Weight at sexual maturity | 3-7 | 5.0 kg | Hovarth et al, 1992 |
29 | Weight at sexual maturity | 2 [Sex not specified] | 2.0 kg | Schlumberger and Proteau, 2001 |
29 | Weight at sexual maturity | The smallest male was 3.744 [12, 1.43 for both sex in other studies] | 3.74 kg | Alp et al, 2004 |
30 | Male sexual dimorphism | Sexual dimorphism is not very pronounced. Females have a comparatively more oval, convex and blunt genital papilla, while male present a more conical papilla and a brush part on the first spin ray of the pectoral fin, but difficulty on distinguishing differences may lead to erros in sexing | Absent | Legendre et al, 1997 |
30 | Male sexual dimorphism | Males grew 2 to 15% faster than females | Absent | Alp et al, 2004 |
31 | Onset of spermatogenesis | End of July-August | ['July', 'August'] | Zholdasova and Guseva, 1987 |
31 | Onset of spermatogenesis | December | ['December'] | Alp et al, 2004 |
32 | Main spermatogenesis activity | September | ['September'] | Zholdasova and Guseva, 1987 |
32 | Main spermatogenesis activity | March-April and May | ['March', 'April', 'May'] | Alp et al, 2004 |
33 | Maximum GSI value | May reach 0.94%, but mean is 0.38% | 0.94 percent | Zholdasova and Guseva, 1987 |
33 | Maximum GSI value | In captivity GSI reaches 1-1.5% | 1.25 percent | Legendre et al, 1997 |
33 | Maximum GSI value | 0.2 [May] | 0.2 percent | Alp et al, 2004 |
34 | Spermatogenesis duration | 2 months [July to September] | 2.0 months | Zholdasova and Guseva, 1987 |
35 | Resting period | 0.12-0.25% at the end of July [June-July] | 3.0 months | Zholdasova and Guseva, 1987 |
35 | Resting period | Low between August and November | 5.0 months | Alp et al, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | No migration | No data | Agence de l'eau, |
37 | Spawning migration period | Leave their winter shelters from the main channel of danube for entering into the spawning areas when water temperature is about 4-6°C | ['January', 'February', 'March'] | Ciolac, 2004 |
39 | Spawning season | May-July | ['May', 'July'] | The Halyn Publishing Group limited, 1976 |
39 | Spawning season | Spawning lasted from the beginning of May to the end of the third week in June | ['May', 'June'] | Horvath, 1977 |
39 | Spawning season | Second half of May | ['May'] | Zholdasova and Guseva, 1987 |
39 | Spawning season | In Dagestan (USSR) catfish spawn at the end of May, but in Polish conditions in mid-june | ['May'] | Wisniewolski, 1988 |
39 | Spawning season | May-June | ['May', 'June'] | Hovarth et al, 1992 |
39 | Spawning season | May-June | ['May', 'June'] | Billard, 1997 |
39 | Spawning season | May-June | ['May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | June, thermophilic species | ['June'] | Ulikowski, 2004 |
39 | Spawning season | June to August | ['June', 'July', 'August'] | Alp et al, 2004 |
39 | Spawning season | May-June | ['May', 'June'] | Fishbase, 2006 |
40 | Spawning period duration | 3-4 [Begins at the end of June and ends in Mid-July] | 3.5 weeks | Zholdasova and Guseva, 1987 |
41 | Spawning temperature | Reared at 23-24°C | 23.5 °C | Horvath, 1977 |
41 | Spawning temperature | 18-19°C | 18.5 °C | Zholdasova and Guseva, 1987 |
41 | Spawning temperature | 22-24 | 23.0 °C | Hovarth et al, 1992 |
41 | Spawning temperature | Spawning can be started as soon as the pond water temperature reaches 20-22°C | 21.0 °C | Legendre et al, 1997 |
41 | Spawning temperature | 20 | 20.0 °C | Mittelbach and Persson, 1998 |
41 | Spawning temperature | 20 [Optimal temperature = 22-25] | 23.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | Exceed 18 | 18.0 °C | Ulikowski, 2004 |
42 | Spawning water type | Spawn in Amudar'ya River, its backwaters and lakes adjacent to the river | Stagnant water | Zholdasova and Guseva, 1987 |
42 | Spawning water type | Between plants, often near roots of trees | Stagnant water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Fish spawning out of the tributary area: carp, pikeperch, catfish Silurus glanis and eel | No category | Hladik and Kubecka, 2003 |
43 | Spawning depth | Shallow waters | No data | Maitland, 1977 |
44 | Spawning substrate | Phytophil | Phytophils | Balon, 1975 |
44 | Spawning substrate | Under vegetation | Phytophils | Maitland, 1977 |
44 | Spawning substrate | Phytophil | Phytophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Sand and mud and located near the roots of tree | Psammophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Over roots | No category | Schlumberger and Proteau, 2001 |
45 | Spawning site preparation | Substratum choosers | No category | Balon, 1975 |
45 | Spawning site preparation | Males buries a nest | No category | The Halyn Publishing Group limited, 1976 |
45 | Spawning site preparation | Eggs are deposited in a hole within the ground | Susbtrate chooser | Billard, 1997 |
45 | Spawning site preparation | The male cleans the nest and after a period of courtship spawning takes place | No category | Legendre et al, 1997 |
45 | Spawning site preparation | Male clear an area | No category | Schlumberger and Proteau, 2001 |
45 | Spawning site preparation | The male opens out a depression in the bottom | No category | Alp et al, 2004 |
45 | Spawning site preparation | Male spawing territories | No category | Ah-King et al, 2004 |
45 | Spawning site preparation | Clutch tenders | No category | Fishbase, 2006 |
45 | Spawning site preparation | Artifical nests installed in spawning grounds | No category | Brzuska and Adamek, 1999 |
47 | Mating system | The aggressiveness of both sexes increase during the spanwing season and heavy injuries occur even during the normal spawning process. Such injuries may later be the cause of death | No category | Horvath, 1977 |
47 | Mating system | By pair: one male and one female | Monogamy | Bruslé and Quignard, 2001 |
47 | Mating system | Spawing in pairs | Monogamy | Ah-King et al, 2004 |
48 | Spawning release | Spawns intermittently [Most female spawns two batches of eggs] | Multiple | Zholdasova and Guseva, 1987 |
48 | Spawning release | After reaching maturity in nature, reproduce only once year | Total | Legendre et al, 1997 |
48 | Spawning release | One clear seasonal peak per year | Total | Fishbase, 2006 |
49 | Parity | Alternate year spawning by some females | No category | Zholdasova and Guseva, 1987 |
49 | Parity | After reaching maturity in nature, reproduce only once year | No category | Legendre et al, 1997 |
50 | Parental care | Males guard eggs until hatching | Male parental care | The Halyn Publishing Group limited, 1976 |
50 | Parental care | Guarded by the male | Male parental care | Legendre et al, 1997 |
50 | Parental care | Male guards eggs | Male parental care | Billard, 1997 |
50 | Parental care | Male guard eggs and discard mud and give oxygen to the eggs | Male parental care | Bruslé and Quignard, 2001 |
50 | Parental care | Male guards eggs | Male parental care | Schlumberger and Proteau, 2001 |
50 | Parental care | The eggs are guarded by the males until they hatch | Male parental care | Alp et al, 2004 |
50 | Parental care | Males guards the nest | Male parental care | Ah-King et al, 2004 |
50 | Parental care | Male guards a cluster of eggs | Male parental care | Fishbase, 2006 |