Trait completeness | 76% |
Total data | 180 |
References | 28 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 3.6-6.0 | 4.8 mm | Barton, 1996 |
1 | Oocyte diameter | 4-5.5 | 4.75 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 3.48-7.64 [Not specified] | 5.56 mm | Bartel et al, 1999 |
1 | Oocyte diameter | 5 | 5.0 mm | Fishbase, 2006 |
1 | Oocyte diameter | 4.5-6 [Not specified] | 5.25 mm | Prawochensky and Kolder, 1968 |
1 | Oocyte diameter | Their equatorial diameter was on average 3.95. In fish farm, found mean size of unswollen eggs 4.4-5.35 mm | 4.88 mm | Penaz and Prihoda, 1981 |
1 | Oocyte diameter | Range: 4.61-6.69, mean 5.38 | 5.65 mm | Purtscher and Humpesch, 2006 |
2 | Egg size after water-hardening | 4.0-5.5 [2 hours after fertilization] | 4.75 mm | Jatteau, 1991 |
2 | Egg size after water-hardening | 3.6-6.0 [Seems to be fertilized eggs] | 4.8 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | Mature roe is light yellow or light orange and about 5 mm in diameter | 5.0 mm | Witokowski and Kokurewicz, 1981 |
2 | Egg size after water-hardening | In our case swelling of the eggs began c. 30 min. after activation and went on intensively for 2 hrs., when the average egg size reached 4.32 mm, though slower swelling and an increase in egg size continued for the first three days of incubation up to a size of 4.55 mm | 4.32 mm | Penaz and Prihoda, 1981 |
2 | Egg size after water-hardening | 4.5 [Fully hardened eggs] | 4.5 mm | Penaz, 1981 |
3 | Egg Buoyancy | Demersal | Demersal | Fishbase, 2006 |
3 | Egg Buoyancy | The eggs of Salmonidae are buried in unguarded nests called 'redds' and are demersal-nonadheive | Demersal | Kunz, 2004 |
4 | Egg adhesiveness | The eggs of Salmonidae are buried in unguarded nests called 'redds' and are demersal-nonadheive | Non-Adhesive | Kunz, 2004 |
4 | Egg adhesiveness | Salmonidae, whose eggs are not sticky | Non-Adhesive | Woynarovich, 1962 |
4 | Egg adhesiveness | The stickiness of the chorion is very low and disappears in washing | Adhesive | Penaz and Prihoda, 1981 |
5 | Incubation time | 138.2 [2°], 50 [6°C], 20.4 [12°C], 13.5 [16°C] | 138.2 days | Jungwirth and Winkler, 1984 |
5 | Incubation time | About 30 | 30.0 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 20 days at 12°C | 20.0 days | Holcik, 1990 |
5 | Incubation time | About 30 | 30.0 days | Perrin, 2001 |
5 | Incubation time | 31 | 31.0 days | Jatteau, 1991 |
5 | Incubation time | Estimates of the number of days required for 50% of egg to hatch: 55 [5°C], 23 [10°C], and 14 [15°C] [In different populations: 32 [At 5.1-16.0°C], 18 [At 4.0-16.0°C]] | 10.55 days | Humpesch, 1985 |
5 | Incubation time | About 3 weeks at 12°C | 3.0 days | Jungwirth, 1978 |
5 | Incubation time | The beginning was on the 31st day, mass hatching begining on the 32nd day, and hathcing finishing on the 34th day at an average temperature of 9.25°C | 31.0 days | Penaz and Prihoda, 1981 |
6 | Temperature for incubation | 5-12 | 8.5 °C | Barton, 1996 |
6 | Temperature for incubation | 6-12 best results, mortality is total above 16°C | 9.0 °C | Jungwirth and Winkler, 1984 |
6 | Temperature for incubation | 4.8-15.5 [Natural conditions], optimal temperaure 10-12°C | 10.15 °C | Jatteau, 1991 |
6 | Temperature for incubation | 8-10 | 9.0 °C | Fishbase, 2006 |
6 | Temperature for incubation | 5.0-13 is the temperature range for >50% survival to hatch [<1.5 and >15.5°C, lethal lower and upper limit] | 9.0 °C | Crisp, 1996 |
6 | Temperature for incubation | Optimum temperature was about 8°C [The lower limit for hatching ca 3°C and the upper limit was between ca. 16 and 20°C] | 8.0 °C | Humpesch, 1985 |
6 | Temperature for incubation | 7°C | 7.0 °C | Prawochensky and Kolder, 1968 |
6 | Temperature for incubation | 12°C | 12.0 °C | Jungwirth, 1978 |
6 | Temperature for incubation | The temperature during the 32-day incubation period fluctuated in the range 4.8-15.5°C | 10.15 °C | Penaz and Prihoda, 1981 |
6 | Temperature for incubation | Average water temperature of 9.25°C | 9.25 °C | Penaz and Prihoda, 1981 |
7 | Degree-days for incubation | 272 | 272.0 °C * day | Barton, 1996 |
7 | Degree-days for incubation | 260-300 | 280.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 240 [20 days at 12°C] | 240.0 °C * day | Holcik, 1990 |
7 | Degree-days for incubation | 232-266 | 249.0 °C * day | Jatteau, 1991 |
7 | Degree-days for incubation | About 200 [19 days at 8-10°C] | 9.0 °C * day | Fishbase, 2006 |
7 | Degree-days for incubation | 230 [i.e. 23 days at 10°C at ca. optimum temperature] | 230.0 °C * day | Humpesch, 1985 |
7 | Degree-days for incubation | 232 DD at 10°C | 232.0 °C * day | Witokowski and Kokurewicz, 1981 |
7 | Degree-days for incubation | 173 [Effective day-degrees] | 173.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | 294 at 7°C | 294.0 °C * day | Prawochensky and Kolder, 1968 |
7 | Degree-days for incubation | The beginning was on 285.5 DD, mass hatching begining on the 301DD, and hathcing finishing on the 331DD at an average temperature of 9.25°C | 285.5 °C * day | Penaz and Prihoda, 1981 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 13-15 | 14.0 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 13-15 [Fry with yolk-sac] | 14.0 mm | Jatteau, 1991 |
8 | Initial larval size | 10.1 mm in length just after hatching obtained at a constant temperature of 10°C | 10.1 mm | Witokowski and Kokurewicz, 1981 |
8 | Initial larval size | The average length of freshly-hatched embryos was 14.1 mm | 14.1 mm | Penaz and Prihoda, 1981 |
9 | Larvae behaviour | Fry remain on the spawning ground until they reach 40 mm | Demersal | Jatteau, 1991 |
9 | Larvae behaviour | Once the vesicle is reabsorbed, young stays near spawning area feeding on bottom fauna | Demersal | Fishbase, 2006 |
9 | Larvae behaviour | The larvae keep close to the ground, near the spawning place | Demersal | Prawochensky and Kolder, 1968 |
9 | Larvae behaviour | After hatching they mostly remain motionless at the bottom of the trough, lying sideways on the yolk sac | Demersal | Penaz and Prihoda, 1981 |
11 | Temperature during larval development | 16-18°C optimum for growth and mortality | 17.0 °C | Jungwirth et al, 1989 |
11 | Temperature during larval development | The maximum temperature for the alevin is 12°C | 12.0 °C | Prawochensky and Kolder, 1968 |
11 | Temperature during larval development | Incubated at 15°C | 15.0 °C | Penaz and Prihoda, 1981 |
12 | Sibling intracohort cannibalism | Cannibalism occurred at fingerling stage in salmonid | Present | Kozlowski and Poczyczynski, 1999 |
12 | Sibling intracohort cannibalism | 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 |
13 | Full yolk-sac resorption | 140-160 | 150.0 °C * day | Bruslé and Quignard, 2001 |
13 | Full yolk-sac resorption | 140-160 | 150.0 °C * day | Jatteau, 1991 |
13 | Full yolk-sac resorption | The larval stage from hatching to the complete resorption of the vitelline sac is about 309°D at 10°C [The feeding to larvae began a few days before the completion of the vitelline sac] | 309.0 °C * day | Witokowski and Kokurewicz, 1981 |
13 | Full yolk-sac resorption | The period from hatching to the loss of the yolk sac is 164.1 DD | 164.1 °C * day | Prawochensky and Kolder, 1968 |
13 | Full yolk-sac resorption | 545 (less than 287.6-339.1 for incubation) yolk sac has disappeared, exlusively external nutrition | 313.35 °C * day | Penaz and Prihoda, 1981 |
14 | Onset of exogeneous feeding | Two or three weeks later they begin feeding (at 12°C) | 12.0 °C * day | Jungwirth, 1978 |
14 | Onset of exogeneous feeding | 457-545 DD (less than 287.6-339.1 for incubation) mixed nutrition | 501.0 °C * day | Penaz and Prihoda, 1981 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4-5 | 4.5 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3-5 | 4.0 year | Barton, 1996 |
15 | Age at sexual maturity | 4-5 [Sex specified] | 4.5 year | Holcik, 1990 |
15 | Age at sexual maturity | 4 [Female] | 4.0 year | Perrin, 2001 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Jatteau, 1991 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Witkowski, 1988 |
15 | Age at sexual maturity | The female reach sexual maturity at the age of 5 years, but also described at 3 or 4 | 5.0 year | Prawochensky and Kolder, 1968 |
15 | Age at sexual maturity | First spawning takes place when fish are 4 or 5 years old [Sex not specified] | 4.0 year | Jungwirth, 1978 |
15 | Age at sexual maturity | Reach sexual maturity after 4-5 years [Sex not specified] | 4.5 year | Jungwirth, 1979 |
15 | Age at sexual maturity | Danubian salmon in pond culture achieve sexual maturity in the 6th-8th year of life | 6.0 year | Penaz and Prihoda, 1981 |
16 | Length at sexual maturity | 70-100 | 85.0 cm | Barton, 1996 |
16 | Length at sexual maturity | Mean of 83.6, range 63.0-94.5 [For female migrating] | 78.75 cm | Witkowski, 1988 |
16 | Length at sexual maturity | At the age of 5 years, female are 65-70 cm long | 67.5 cm | Prawochensky and Kolder, 1968 |
16 | Length at sexual maturity | Average length of 70 cm [Sex not specified] | 70.0 cm | Jungwirth, 1979 |
17 | Weight at sexual maturity | 2-3 | 2.5 kg | Holcik, 1990 |
17 | Weight at sexual maturity | Mean of 6.1, range 2.5-8.3 [For female migrating] | 5.4 kg | Witkowski, 1988 |
17 | Weight at sexual maturity | At the age of 5 years, female weights about 3.5 | 5.0 kg | Prawochensky and Kolder, 1968 |
17 | Weight at sexual maturity | First spawning takes place when fish are 3 or 4 kg [Sex not specified] | 3.0 kg | Jungwirth, 1978 |
17 | Weight at sexual maturity | 4 [Sex not specified] | 4.0 kg | Jungwirth, 1979 |
19 | Relative fecundity | 1.1.6 | 1.1 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 1-1.6 | 1.3 thousand eggs/kg | Jatteau, 1991 |
19 | Relative fecundity | 1.2-1.5 | 1.35 thousand eggs/kg | Jungwirth, 1978 |
19 | Relative fecundity | Relative fertility of 1095 to 3330 pieces | 1095.0 thousand eggs/kg | Penaz and Prihoda, 1981 |
20 | Absolute fecundity | 1-1.6 | 1.3 thousand eggs | Barton, 1996 |
20 | Absolute fecundity | Absolute fertility range from 2500-18000, but could even reach 25000 | 10250.0 thousand eggs | Witokowski and Kokurewicz, 1981 |
20 | Absolute fecundity | 2.4 [For female 3-5 kg], 3-4 [4-5 kg], 5-6 [6-8 kg], 8-12 [10-12 kg], 18.6 [18 kg] | 4.0 thousand eggs | Prawochensky and Kolder, 1968 |
20 | Absolute fecundity | Useful fertility 12500-22500 pieces | 17500.0 thousand eggs | Penaz and Prihoda, 1981 |
24 | Maximum GSI value | Mean of 15.5% for different populations | 15.5 percent | Fleming, 1998 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3-4 | 3.5 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 3-4 [Sex specified] | 3.5 years | Holcik, 1990 |
27 | Age at sexual maturity | 3 [Male] | 3.0 years | Perrin, 2001 |
27 | Age at sexual maturity | 3-4 [Male] | 3.5 years | Jatteau, 1991 |
27 | Age at sexual maturity | 3-4 [Male, the males mature a year before than females] | 3.5 years | Witkowski, 1988 |
28 | Length at sexual maturity | Mean of 83.2, range 58.3-109.0 [For male migrating] | 83.65 cm | Witkowski, 1988 |
29 | Weight at sexual maturity | 1-2 | 1.5 kg | Holcik, 1990 |
29 | Weight at sexual maturity | Mean of 6.6, range 2.1-14.2 [For male migrating] | 8.15 kg | Witkowski, 1988 |
29 | Weight at sexual maturity | First spawning takes place when fish are 3 or 4 kg [Sex not specified] | 3.0 kg | Jungwirth, 1978 |
30 | Male sexual dimorphism | Breeding tubercles present | Present | Kratt and Smith, 1978 |
30 | Male sexual dimorphism | The males undergo marked colour changes, turning red or copper-red | Absent | Prawochensky and Kolder, 1968 |
30 | Male sexual dimorphism | Males are bigger than females | Absent | Fleming, 1998 |
33 | Maximum GSI value | Mean of 3 for different populations | 3.0 percent | Fleming, 1998 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Low ampliture about 5-15 km | 10.0 km | Bruslé and Quignard, 2001 |
36 | Spawning migration distance | Move upstream to spawning sites, but these migrations are short, not exceeding 10-25 km | 17.5 km | Holcik, 1990 |
36 | Spawning migration distance | Migration during night of about 5-20 km | 12.5 km | Perrin, 2001 |
36 | Spawning migration distance | Short migrations: from 5 to 10-25 km | 17.5 km | Jatteau, 1991 |
36 | Spawning migration distance | Does not undertake large migrations. Unless disturbed, it makes only local migrations in seach of spawning places | No data | Prawochensky and Kolder, 1968 |
37 | Spawning migration period | Most often the migration starts between April 7 and 10, with water 7-8°C warm [Duration of migration varies from 6 days to 1.5 months depending on environmental conditions] | ['April'] | Witkowski, 1988 |
37 | Spawning migration period | Represents the largest exclusively riverine and non-migratory salmonid fish | No data | Jungwirth, 1979 |
38 | Homing | Seem to display the same homing of salmon | Present | Bruslé and Quignard, 2001 |
38 | Homing | Homing behavior | Present | Jatteau, 1991 |
39 | Spawning season | March-April | ['March', 'April'] | Billard, 1997 |
39 | Spawning season | Spring: Mid-March until Mid-April, up to May | ['March', 'April', 'May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | April | ['April'] | Perrin, 2001 |
39 | Spawning season | March-April | ['March', 'April'] | Jatteau, 1991 |
39 | Spawning season | April-May | ['April', 'May'] | Fishbase, 2006 |
39 | Spawning season | On the south of Europe spawning starts as soon as February and lasts until March and in Central Europe it extends from April to mid-May | ['February', 'March', 'April', 'May'] | Witkowski, 1988 |
39 | Spawning season | Spring spawner [Other authors described between March and May] | ['March', 'April', 'May', 'June'] | Humpesch, 1985 |
39 | Spawning season | The spawning begins in April (the earliest spawning was noted on April 6, at water temperature of 3.6°C) and lasts to mid July (the last spawning was observed on May 13, at water temperature of 9.2°C). The most intense spawning usually occurs by the end of April at water temperature of about 7°C | ['April', 'May', 'July'] | Witokowski and Kokurewicz, 1981 |
39 | Spawning season | Spring spawner, it spawns in March and April | ['March', 'April', 'May', 'June'] | Prawochensky and Kolder, 1968 |
39 | Spawning season | Depending on the local water temperature spawning takes place between the middle of March and end of April | ['March', 'April'] | Jungwirth, 1978 |
39 | Spawning season | The ripening of the sexual products of Danubian salmon takes place in the spring months, especially in the second half of April and first half of May | ['April', 'May', 'June'] | Penaz and Prihoda, 1981 |
40 | Spawning period duration | 5-6 [On the south of Europe spawning starts as soon as February and lasts until March] | 5.5 weeks | Witkowski, 1988 |
40 | Spawning period duration | The earliest spawning was noted on April 6, to mid July (the last spawning was observed on May 13 (the most intense spawning usually occurs by the end of April) | 6.0 weeks | Witokowski and Kokurewicz, 1981 |
40 | Spawning period duration | In Poland, the spawning time is between April 20 and 26, in Yugoslavia in the Drava river, between march 18 and 22 | 20.0 weeks | Prawochensky and Kolder, 1968 |
40 | Spawning period duration | Annual spawning period in free rivers is relatively short | No data | Jungwirth, 1979 |
41 | Spawning temperature | 6-10 | 8.0 °C | Barton, 1996 |
41 | Spawning temperature | 8-10 | 9.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 5-10 | 7.5 °C | Holcik, 1990 |
41 | Spawning temperature | 8-10 | 9.0 °C | Perrin, 2001 |
41 | Spawning temperature | 8-10 | 9.0 °C | Jatteau, 1991 |
41 | Spawning temperature | Species starts spawning at 6-10°C | 8.0 °C | Witkowski, 1988 |
41 | Spawning temperature | The earliest spawning was noted at water temperature of 3.6°C and last spawning was observed at water temperature of 9.2°C. The most intense spawning usually occurs at water temperature of about 7°C | 3.6 °C | Witokowski and Kokurewicz, 1981 |
41 | Spawning temperature | 5-10, mainly 5-6°C | 7.5 °C | Prawochensky and Kolder, 1968 |
41 | Spawning temperature | When the water temperature, at least during the day, exceeds 8°C | 8.0 °C | Penaz and Prihoda, 1981 |
42 | Spawning water type | Water velocities : 0.61 m/s | Flowing or turbulent water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Perrin, 2001 |
42 | Spawning water type | Water with current: 0.6-1 m/s | Flowing or turbulent water | Jatteau, 1991 |
42 | Spawning water type | Migrate upstream into smaller and shallower streams | No category | Fishbase, 2006 |
42 | Spawning water type | Rivers and larger streams on the region of the grayling | No category | Witokowski and Kokurewicz, 1981 |
42 | Spawning water type | Upper courses of highland rivers, where the stream runs fairly rapidly | No category | Prawochensky and Kolder, 1968 |
43 | Spawning depth | 0.30-1.20 | 0.75 m | Bruslé and Quignard, 2001 |
43 | Spawning depth | 0.3-1.2 m | 0.75 m | Jatteau, 1991 |
43 | Spawning depth | 0.3-1.5 | 0.9 m | Fishbase, 2006 |
43 | Spawning depth | Often chooses for spawning the stream section with a depth from 0.4-0.6 m | 0.5 m | Witkowski, 1988 |
43 | Spawning depth | 60-100 cm | 80.0 m | Witokowski and Kokurewicz, 1981 |
43 | Spawning depth | 30-60 cm | 45.0 m | Prawochensky and Kolder, 1968 |
43 | Spawning depth | Average depth of one meter | No data | Jungwirth, 1978 |
44 | Spawning substrate | Gravels | Lithophils | Billard, 1997 |
44 | Spawning substrate | Small gravels | Lithophils | Perrin, 2001 |
44 | Spawning substrate | Sand or gravels | Lithophils | Jatteau, 1991 |
44 | Spawning substrate | Sand or gravels | Lithophils | Fishbase, 2006 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Gravelly and sandy bottom | Lithophils | Witokowski and Kokurewicz, 1981 |
44 | Spawning substrate | Bottom is covered with gravel or coarse sand | Lithophils | Prawochensky and Kolder, 1968 |
44 | Spawning substrate | Fist-sized loose gravel | Lithophils | Jungwirth, 1978 |
45 | Spawning site preparation | Female dig a nest | Susbtrate chooser | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Eggs are buried within 40 cm deep | No category | Perrin, 2001 |
45 | Spawning site preparation | Female dig a nest 30-40 cm deep, and 120-150 cm wide | Susbtrate chooser | Jatteau, 1991 |
45 | Spawning site preparation | Female dig a nest [Brood hiders] | Susbtrate chooser | Fishbase, 2006 |
45 | Spawning site preparation | Brood hiders | Susbtrate chooser | Balon, 1975 |
45 | Spawning site preparation | The female is aided by the male in making a nest 120-150 cm in width and 3040 cm in depth, in the bottom of the river | No category | Witokowski and Kokurewicz, 1981 |
45 | Spawning site preparation | Female sets to work to scoop out a shallow, saucer-like depression, 25-60 cm deep, by means of vigorous, flapping movements of her body and tail, may take several days [During the spawning period, the males are generally very fierce, driving away intruders with great pugnacity and vigour, or engagin in formal combats with other males] | No category | Prawochensky and Kolder, 1968 |
45 | Spawning site preparation | Nest by females | Best build by female | Fleming, 1998 |
47 | Mating system | By pair, males and females are very aggressive | Monogamy | Jatteau, 1991 |
47 | Mating system | Spawn in pairs | Monogamy | Witkowski, 1988 |
48 | Spawning release | Eggs are buried in spawning redds | No category | Holcik, 1990 |
49 | Parity | Iteroparous : 8-12 spawning during a lifetime | Iteroparous | Bruslé and Quignard, 2001 |
49 | Parity | The fishes spawning represented nine age groups: 4 to 12 years | No category | Witkowski, 1988 |
49 | Parity | The reproduction is annual | No category | Jatteau, 1991 |
49 | Parity | Spawning takes place once a year | Iteroparous | Prawochensky and Kolder, 1968 |
49 | Parity | They are known to spawn up to 12 times per lifetime | No category | Jungwirth, 1978 |
49 | Parity | Mean of 64 (range 51-77%) of repeat spawners | No category | Fleming, 1998 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |
50 | Parental care | There is no parental care during the hatching or embryonic phase [After spawning, the parent fish go downstream and keep close to deep places and rocks] | No care | Prawochensky and Kolder, 1968 |
50 | Parental care | No defence by females | No care | Fleming, 1998 |