Trait completeness | 76% |
Total data | 98 |
References | 16 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 2.2-2.4 | 2.3 mm | Belyaeva, 2005 |
1 | Oocyte diameter | Average 2.5 | 2.5 mm | Fishbase, 2006 |
1 | Oocyte diameter | Up to 2.4 [Not specified] | 2.4 mm | Coad, 2006 |
2 | Egg size after water-hardening | 3.1-3.2 | 3.15 mm | Sturn, 1994 |
2 | Egg size after water-hardening | 3.1-3.2 [Fully hardened eggs] | 3.15 mm | Penaz, 1981 |
3 | Egg Buoyancy | Demersal [Deposited on the bottom] | Demersal | Belyaeva, 2005 |
3 | Egg Buoyancy | Demersal [On the bottom] | 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 | Semi-adhesive | Adhesive | Belyaeva, 2005 |
4 | Egg adhesiveness | Slightly adhesive | Adhesive | Coad, 2006 |
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 |
5 | Incubation time | 180-220 | 200.0 days | Belyaeva, 2005 |
5 | Incubation time | 250-260 | 255.0 days | Chereshnev et al, 2000 |
5 | Incubation time | 180-200 | 190.0 days | Coad, 2006 |
6 | Temperature for incubation | 0.1-1.2 | 0.65 °C | Belyaeva, 2005 |
6 | Temperature for incubation | 4.0 | 4.0 °C | Sturn, 1994 |
6 | Temperature for incubation | Range limits: 0.1-8 | 4.05 °C | Mack and Billard, 1984 |
7 | Degree-days for incubation | 180-200 [180-220 at 0.1-1.2°C] | 190.0 °C * day | Belyaeva, 2005 |
7 | Degree-days for incubation | 360, i.e. about 91 at 4°C | 360.0 °C * day | Sturn, 1994 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 11 | 11.0 mm | Belyaeva, 2005 |
8 | Initial larval size | Average 13.2, range 12.6-14.3 | 13.45 mm | Chereshnev et al, 2000 |
8 | Initial larval size | 12.5, mass hatching | 12.5 mm | Bogdanova, 1978 |
8 | Initial larval size | 11.0-11.3 | 11.15 mm | Sturn, 1994 |
11 | Temperature during larval development | 1.2-10.6 | 5.9 °C | Belyaeva, 2005 |
11 | Temperature during larval development | Two tests: 2.2-6 and 8.8-13.8 | 4.1 °C | Bogdanova, 1978 |
11 | Temperature during larval development | From 4 to 14 | 4.0 °C | Sturn, 1994 |
13 | Full yolk-sac resorption | 115 [Around 11 days at 11.4°C, the last remnants of the yolk has disappeared and 23 days at 3.8°C] | 115.0 °C * day | Bogdanova, 1978 |
13 | Full yolk-sac resorption | 130 [33 days at 4°C] | 130.0 °C * day | Sturn, 1994 |
14 | Onset of exogeneous feeding | About 30 [Mixed feeding at 3 days at 11.4°C, and 7 days at 3.8°C] | 30.0 °C * day | Bogdanova, 1978 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 6-7 | 6.5 year | Belyaeva, 2005 |
15 | Age at sexual maturity | 7-10 [Sex not specified] | 8.5 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | 10-12 [Female] | 11.0 year | Fishbase, 2006 |
15 | Age at sexual maturity | Mass maturation for females at 10-12 [But could be as early as 8] | 11.0 year | Chereshnev et al, 2000 |
15 | Age at sexual maturity | 8-10 [Not specified] | 9.0 year | Maitland, 1977 |
16 | Length at sexual maturity | 70-75 | 72.5 cm | Fishbase, 2006 |
16 | Length at sexual maturity | Mass maturation for females at 70-75 [But could be as 66.2] | 72.5 cm | Chereshnev et al, 2000 |
17 | Weight at sexual maturity | Mass maturation for females at 4.0-5.0 [But could be 2.53] | 4.5 kg | Chereshnev et al, 2000 |
17 | Weight at sexual maturity | 5.65 pounds at 7 years and 9.75 pounds at 10 years | 5.65 kg | Scott and Crossman, 1973 |
18 | Female sexual dimorphism | The inconnu exhibits little external difference between the sexes, although females can be slightly bigger than same-age males | Absent | Willson, 1997 |
19 | Relative fecundity | 18-35 eggs per 1 g of body weight, not viscera. Also described that the absolute fecundity ranges from 80000 to 420000, for female ranging from means of 3.35 [At 11 years old] to 9.74 [At 17 years old] | 26.5 thousand eggs/kg | Chereshnev et al, 2000 |
19 | Relative fecundity | 23.74 ± 1.14 (group I, n = 12) and 21.24 ± 0.85 (group II, n =26) | 23.74 thousand eggs/kg | Dyubin, 2007 |
20 | Absolute fecundity | 160-400 | 280.0 thousand eggs | Belyaeva, 2005 |
20 | Absolute fecundity | 125-325 | 225.0 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | 80-420 | 250.0 thousand eggs | Chereshnev et al, 2000 |
20 | Absolute fecundity | 130-400 | 265.0 thousand eggs | Maitland, 1977 |
23 | Intensifying oogenesis activity | July-August [From 7.8% to 18.3%] | ['July', 'August'] | Chereshnev et al, 2000 |
24 | Maximum GSI value | Mean 18.3 but up to 23.5 [First ten day period of August] | 18.3 percent | Chereshnev et al, 2000 |
24 | Maximum GSI value | 26.25 ± 2.02 | 26.25 percent | Kychanov, 1982 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 5-6 | 5.5 years | Belyaeva, 2005 |
27 | Age at sexual maturity | 7-10 [Sex not specified] | 8.5 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | 9-11 [Male] | 10.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | Mass maturation for males at 9-11 [But could be as early as 7] | 10.0 years | Chereshnev et al, 2000 |
28 | Length at sexual maturity | 65-70 | 67.5 cm | Fishbase, 2006 |
28 | Length at sexual maturity | Mass maturation for males at 65-70 [But could be as 54.0] | 67.5 cm | Chereshnev et al, 2000 |
29 | Weight at sexual maturity | Mass maturation for females at 2.0-3.5 [But could be 1.47] | 2.75 kg | Chereshnev et al, 2000 |
30 | Male sexual dimorphism | Males develop tubercles on the head and sides of the abdomen during spawning | Absent | Coad, 2006 |
33 | Maximum GSI value | 2.72 ± 0.08 | 2.72 percent | Kychanov, 1982 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Up to 3000 km | 3000.0 km | Belyaeva, 2005 |
37 | Spawning migration period | The upstream, presumably prespawning migration, is prolonged and apparently continues all summer | ['July', 'August', 'September'] | Scott and Crossman, 1973 |
37 | Spawning migration period | Upstream migration from wintering areas begins at ice break-up | ['January', 'February', 'March'] | Fishbase, 2006 |
37 | Spawning migration period | The prespawning nelma begins migration to its spawning grounds before the ice drift, the mass migration is observed in the first half of June | ['June'] | Chereshnev et al, 2000 |
37 | Spawning migration period | The Caspian inconnu migration into the Volga mouth began in September-Ocotber when the water temperature decreased down to 18-19°C, and it went on 6-7 months | ['September'] | Dyubin, 2007 |
39 | Spawning season | October-November | ['October', 'November'] | Belyaeva, 2005 |
39 | Spawning season | Late summer or earty autumn | ['July', 'August', 'September', 'October', 'November', 'December'] | Scott and Crossman, 1973 |
39 | Spawning season | September to October | ['September', 'October'] | Fishbase, 2006 |
39 | Spawning season | Mass spawning of nelma begins in middle to late September | ['September'] | Chereshnev et al, 2000 |
39 | Spawning season | Spawning takes place in October and November | ['October', 'November'] | Coad, 2006 |
39 | Spawning season | October-November | ['October', 'November'] | Maitland, 1977 |
39 | Spawning season | In summer and early fall | ['July', 'August', 'September', 'October', 'November', 'December'] | Willson, 1997 |
40 | Spawning period duration | 6-8 [Spawning takes place in October and November] | 7.0 weeks | Coad, 2006 |
41 | Spawning temperature | Falls to 6°C | 6.0 °C | Belyaeva, 2005 |
41 | Spawning temperature | 3-6°C | 4.5 °C | Chereshnev et al, 2000 |
41 | Spawning temperature | 0.2-6°C | 3.1 °C | Coad, 2006 |
41 | Spawning temperature | Spawning which occurred at the water temperature of 0.2-6.0°C | 3.1 °C | Dyubin, 2007 |
42 | Spawning water type | Wide areas | No category | Chereshnev et al, 2000 |
42 | Spawning water type | Usually in mid and inferior part of big streams | No category | Maitland, 1977 |
42 | Spawning water type | Streams | No category | Willson, 1997 |
43 | Spawning depth | Shallow | No data | Belyaeva, 2005 |
43 | Spawning depth | Near the surface | No data | Fishbase, 2006 |
43 | Spawning depth | Depth 2-3 m | 2.5 m | Chereshnev et al, 2000 |
44 | Spawning substrate | Grounds covered with sand and gravel | Lithophils | Belyaeva, 2005 |
44 | Spawning substrate | Sandy-pebbly bottom | Psammophils | Chereshnev et al, 2000 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
45 | Spawning site preparation | Open water / substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | The eggs are shed on the river bottom | No category | Coad, 2006 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
45 | Spawning site preparation | Brood hiders | Susbtrate chooser | Balon, 1975 |
46 | Nycthemeral period of oviposition | Spawning begins at dusk, and continuing well into the night | Night | Fishbase, 2006 |
47 | Mating system | A female accompanied by a male swims to the surface near the upstream end of the spawning ground [Female may repeat the spawning act over the downstream portion of the spawning area or may move upstream to the head of the grounds before releaseing more eggs] | No category | Fishbase, 2006 |
48 | Spawning release | Once | Total | Belyaeva, 2005 |
48 | Spawning release | Female may repeat the spawning act over the downstream portion of the spawning area or may move upstream to the head of the grounds before releasing more eggs | No category | Fishbase, 2006 |
49 | Parity | Twice in his lifecycle, with an interval of 2-3 years | No category | Belyaeva, 2005 |
49 | Parity | Suspected that individual fish spawn only once every 2, 3 or 4 years | No category | Scott and Crossman, 1973 |
49 | Parity | Russian fish appear to spawn only every third or fourth year | No category | Fishbase, 2006 |
49 | Parity | Spawning occur only once or twice in the life cycle of most fish although exceptional famesl may spawn 3 times [spawning occur at intervals of 2-3 years] | No category | Coad, 2006 |
49 | Parity | Live up to 20 years | No category | Maitland, 1977 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |