Trait completeness | 88% |
Total data | 216 |
References | 26 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.3-1.4 | 1.35 mm | Coad, 2005 |
1 | Oocyte diameter | 1.43 | 1.43 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 3 fractions of spawn with average grain of 1.4, 0.9 and 0.6 mm | 0.6 mm | Wajdowicz, 1974 |
1 | Oocyte diameter | Two size groups of eggs were found in gonads, the first of size 1.15-1.63 mm in stage "E", the second with size 0.4-0.6 mm in stage "C". The mean egg size was 1.33 mm (1.26-1.41 mm). We obtained 9500 eggs (mean diameter 1.51 mm) from the female with SL= 213mm (age 5 years), and 7400 eggs (mean diameter 1.46 mm) from the female with Sl= 188 mm(age 4 years) | 1.39 mm | Lusk et al, 2005 |
1 | Oocyte diameter | Egg diameter from the first batch is the largest (approx. 1.4 mm); in the final batch, eggs are much smaller (approx. O.6 mm in diameter). | 1.4 mm | Luszczek et al, 2008 |
2 | Egg size after water-hardening | After fertilization the spawn of V. Vimba from the Czarna Orawa, similarly as that from the catchment area of the Baltic Sea, swells greatly in water, its volume increasing about twice | No data | Wajdowicz, 1974 |
2 | Egg size after water-hardening | 2.0 [Not specified] | 2.0 mm | Kamler and Wolnicki, 2006 |
2 | Egg size after water-hardening | The mean egg size on the 3rd day of incubation reached 1.95 mm (1.90-2.05 mm). | 1.97 mm | Lusk et al, 2005 |
3 | Egg Buoyancy | Demersal [Deposit on gravel and stones] | Demersal | Coad, 2005 |
3 | Egg Buoyancy | The fertilized spawn adheres to the stones or becomes covered by the gravel of the river bottom | Demersal | Wajdowicz, 1974 |
3 | Egg Buoyancy | Fertilized eggs drifting with the current fall upon the stony - gravel bottom | Demersal | Trzebiatowski and Narozanski, 1973 |
4 | Egg adhesiveness | The eggs are very sticky | Adhesive | Shikhshabekov, 1979 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | The fertilized spawn adheres to the stones or becomes covered by the gravel of the river bottom | Adhesive | Wajdowicz, 1974 |
4 | Egg adhesiveness | Fertilized eggs were seperated using water-diluted milk and placed in 1.5 litre hatching jars. | Non-Adhesive | Lusk et al, 2005 |
4 | Egg adhesiveness | The current study demonstrated that eggs of common carp (and of vimba, bleak and chub in unpublished data) became sticky within seconds after mixing with water and already 30 s after water contact was enough to develop the egg stickiness mechanism | Adhesive | Mansour et al, 2008 |
4 | Egg adhesiveness | Owing to their viscosity, become attached to the substrate | Adhesive | Trzebiatowski and Narozanski, 1973 |
5 | Incubation time | 3-3.5 | 3.25 days | Coad, 2005 |
5 | Incubation time | 2-3 | 2.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 2-10 | 6.0 days | Keith and Allardi, 2001 |
5 | Incubation time | 8.2 [13.2°C], 3 [19.1°C] | 8.2 days | Herzig and Winkler, 1986 |
5 | Incubation time | 5-10 | 7.5 days | Maitland, 1977 |
5 | Incubation time | 5 at about 18-20°C [Also described at 3.5-4 days at 13-15°C] | 19.0 days | Wajdowicz, 1974 |
5 | Incubation time | Hatching occurred on the 5th day within 6 hours after reaching 80-90 degree-days | 85.0 days | Lusk et al, 2005 |
5 | Incubation time | Embryonic development lasts for 3-4 days at 20-24°C, but can extend to 7 days at lower temperatures | 3.5 days | Luszczek et al, 2008 |
6 | Temperature for incubation | 17-22 | 19.5 °C | Coad, 2005 |
6 | Temperature for incubation | 12-20 for embryonic development, 10-23 in which normal development occurs and 10-11 lower lethal temperature and >24 upper lethal temperature | 16.0 °C | Herzig and Winkler, 1986 |
6 | Temperature for incubation | About 16-18°C [When during the incubation time the water temperature fell below 11-12°C, the development of the embryos was distinctly inhibited and those born were not vital] | 17.0 °C | Wajdowicz, 1974 |
6 | Temperature for incubation | Eggs incubated at 25 ± 0.5°C | 25.0 °C | Hliwa et al, 2003 |
6 | Temperature for incubation | Viable range 10-24, threshold temperature at which ontogeny is theoretically arrested: 10.1 | 17.0 °C | Kamler and Wolnicki, 2006 |
6 | Temperature for incubation | Water flowing through the apparatus had a temperature of 15-16°C, rising at the end of incubation to 17°C | 15.5 °C | Lusk et al, 2005 |
6 | Temperature for incubation | 20-24°C | 22.0 °C | Luszczek et al, 2008 |
7 | Degree-days for incubation | 50-70 [70-77 hours at 17-22°C] | 60.0 °C * day | Coad, 2005 |
7 | Degree-days for incubation | About 50-80 | 65.0 °C * day | Wajdowicz, 1974 |
7 | Degree-days for incubation | 28 [Effective day-degrees] | 28.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | Hatching occurred on the 5th day within 6 hours after reaching 80-90 degree-days | 85.0 °C * day | Lusk et al, 2005 |
7 | Degree-days for incubation | Embryonic development lasts for 3-4 days at 20-24°C, but can extend to 7 days at lower temperatures | 3.5 °C * day | Luszczek et al, 2008 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 5.5 | 5.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | Larvae hatched in the VII th development stage at a mean length of 4.7 mm, eyes without pigmentation and pectoral fins just beginning to form | 4.7 mm | Lusk et al, 2005 |
9 | Larvae behaviour | Hathing proceeds initially in hiding between stones. Then, after a few days, the hatched fish either swim actively down the river or are swept down by the current to the reservoir | Demersal | Wajdowicz, 1974 |
10 | Reaction to light | Initially the larvae are photophobic | Photophobic | Mann, 1996 |
11 | Temperature during larval development | Vimba larvae were raised at a constant temperature of 25 ± 0/5°C | 25.0 °C | Hliwa et al, 2003 |
11 | Temperature during larval development | Reared at 25°C | 25.0 °C | Kamler and Wolnicki, 2006 |
11 | Temperature during larval development | Tested temperature 19, 22, 25, 28, and 31°C | 19.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | Optimum temperatures for larval growth (expressed as Relative growth rate: RGR, %d): 19-30°C | 24.5 °C | Wolnicki, 2005 |
11 | Temperature during larval development | The average temperature was 24.0 ± 0.5°C, pH 8.6 ± 0.2, and dissolved oxygen 7.9 ± 0.3 mg.l-1. | 24.0 °C | Ostaszewska et al, 2008 |
11 | Temperature during larval development | Water temperature was established to 23 ± 1°C and was monitered continously in 1-hour interval | 23.0 °C | Hamackova et al, 2009 |
13 | Full yolk-sac resorption | Yolk resorption last up to 14 days | 14.0 °C * day | Luszczek et al, 2008 |
14 | Onset of exogeneous feeding | First feeding larvae age 5 days post-hatching at 20°C, Lt 7.8 ± 0.2 mm, body weight 2.0 ± 0.2 mg | 7.8 °C * day | Wolnicki, 2005 |
14 | Onset of exogeneous feeding | The larvae (2 ± 0.34 mg, 8.4 ± 0.24 mm) were fed from the sixth day after hatching . The average temperature was 24.0 ± 0.5°C, pH 8.6 ± 0.2, and dissolved oxygen 7.9 ± 0.3 mg.l-1. | 2.0 °C * day | Ostaszewska et al, 2008 |
14 | Onset of exogeneous feeding | Larvae begin to swim freely 7 days after hatching, and feed on day later | 7.0 °C * day | Luszczek et al, 2008 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 3 | 3.0 year | Shikhshabekov, 1979 |
15 | Age at sexual maturity | 3 | 3.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 2-3 | 2.5 year | Coad, 2005 |
15 | Age at sexual maturity | 4-5 | 4.5 year | Hliwa and Martyniak, 2002 |
15 | Age at sexual maturity | 5 and more | 5.0 year | Hliwa et al, 2002 |
15 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 year | Keith and Allardi, 2001 |
15 | Age at sexual maturity | 3 [Unsexed] | 3.0 year | Fishbase, 2006 |
15 | Age at sexual maturity | 3-4 [Not specified] | 3.5 year | Maitland, 1977 |
15 | Age at sexual maturity | Marked inhibition of the growth rate of the body length took place after the fifth year of life, thus after reaching sexual maturity, this being usually more pronounced in females | 5.0 year | Wajdowicz, 1974 |
15 | Age at sexual maturity | Vimba mature in the 2nd and 3rd year of life. The caspian vimba matures at the age of 3. Fish of age 2-5 participate in spawning, and 4-year-old fish are predominant in the spawning population. | 3.5 year | Kuliev, 1988 |
15 | Age at sexual maturity | females become mature at the age 6. A common age of spawning vimba is 6-7 years | 6.5 year | Kesminas et al, 1999 |
15 | Age at sexual maturity | The rapid growth facilitates an early maturation of the vimba: both males and females become sexually mature at the age of 3-5 years | 4.0 year | Ermolin and Shashulovskii, 2006 |
15 | Age at sexual maturity | The fourth age group almost exclusively comprised males, females being rarely encoutered. This indicates that males reach the maturity state in their fourth year of life, i.e., a year earlizer than females | 4.0 year | Trzebiatowski and Narozanski, 1973 |
15 | Age at sexual maturity | Under natural conditions, vimba becomes sexually mature at 4-5 years of age, although 3-year-old females have been found in spawning schools in the moutain tributaries of the Vistula River; in the Vistula lagoon, wimba first enter reproduction at the age of 7-8 years | 4.5 year | Luszczek et al, 2008 |
16 | Length at sexual maturity | 15-31 | 23.0 cm | Shikhshabekov, 1979 |
16 | Length at sexual maturity | >27 | 27.0 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | 16-23 [Length of most spawning females] | 19.5 cm | Coad, 2005 |
16 | Length at sexual maturity | 24 | 24.0 cm | Hliwa and Martyniak, 2002 |
16 | Length at sexual maturity | 22.2-34.0 | 28.1 cm | Hliwa et al, 2002 |
16 | Length at sexual maturity | The average of body length of spawners caught in 1969 and 1970 was about 36 cm [Both sex] | 36.0 cm | Wajdowicz, 1974 |
16 | Length at sexual maturity | The major part of the spawning population consists of 16-23 cm females. In all studied year, mature females ranges from 13.5-17.8 [Age 3]; 16.8-18.9 [Age 4], 19.4-20.9 [Age 5] | 19.5 cm | Kuliev, 1988 |
16 | Length at sexual maturity | Migrating females are 28-30 cm long. A common size is 25.5-29.6 cm | 29.0 cm | Kesminas et al, 1999 |
16 | Length at sexual maturity | Spawners used in the experiments were 5-7+, and size was 24.9 ± 2.45 | 24.9 cm | Hliwa et al, 2003 |
16 | Length at sexual maturity | 845 spawners with the body length (logitudo corporis) ranging from 24.5 to 40.5 cm and the total length (longitudo totalis) range of 29.5-48.5 cm | 39.0 cm | Trzebiatowski and Narozanski, 1973 |
17 | Weight at sexual maturity | 0.045-0.41 | 0.23 kg | Shikhshabekov, 1979 |
17 | Weight at sexual maturity | 0.166-0.693 | 0.43 kg | Hliwa et al, 2002 |
17 | Weight at sexual maturity | The average of body weight of spawners caught in 1969 and 1970 was about over 0.460 kg [Both sex] | 1969.0 kg | Wajdowicz, 1974 |
17 | Weight at sexual maturity | In all studied year, mature females ranges from 48-114 g [Age 3]; 89-140 [Age 4], 133-177 [Age 5] | 81.0 kg | Kuliev, 1988 |
17 | Weight at sexual maturity | A common weight for both sex is 331-408 g | 369.5 kg | Kesminas et al, 1999 |
17 | Weight at sexual maturity | Spawners used in the experiments were 5-7+, and size was 239.4 ± 93.6 | 239.4 kg | Hliwa et al, 2003 |
18 | Female sexual dimorphism | Females may also develop tubercules but to a lesser extent | Absent | Coad, 2005 |
18 | Female sexual dimorphism | As a rule, the females are slightly larger than males of the same age | Absent | Kuliev, 1988 |
19 | Relative fecundity | 25.6-120.1 | 72.85 thousand eggs/kg | Hliwa and Martyniak, 2002 |
19 | Relative fecundity | 34.5-74.5 thousands grains | 54.5 thousand eggs/kg | Wajdowicz, 1974 |
19 | Relative fecundity | In eight females with mean SL=196.7 mm (188-213 mm) and mean weight 149.1 g (126-175 g), the relative fecundity varied between 133000 to 155000 eggs per kg of female weight (mean 133000 eggs per kg) | 200.5 thousand eggs/kg | Lusk et al, 2005 |
19 | Relative fecundity | The individual fecundity of the investigated Rega vimbs of the body lengths ranging within 25.0-38.0 cm amounts to 33800-139000 eggs (the mean value 77500), while its relative fecundity ranges from 81000 to 159000 eggs per 1 kg of fish (the mean value is 114600) [...] Other studies: With the body length range of 25.0-38.0 cm to vary from 40000 to 100000 eggs, the mean value being 66000 [...] Niemen vimbs within the range of 38000-130000 (the mean valu 73,600) | 31.5 thousand eggs/kg | Trzebiatowski and Narozanski, 1973 |
20 | Absolute fecundity | 89.2-200 | 144.6 thousand eggs | Coad, 2005 |
20 | Absolute fecundity | 100-300 | 200.0 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 9.56-157 | 83.28 thousand eggs | Hliwa and Martyniak, 2002 |
20 | Absolute fecundity | 25-150 | 87.5 thousand eggs | Keith and Allardi, 2001 |
20 | Absolute fecundity | 15-20 at the age of 6-7 years | 17.5 thousand eggs | Fishbase, 2006 |
20 | Absolute fecundity | 25-115 | 70.0 thousand eggs | Maitland, 1977 |
20 | Absolute fecundity | With an average body weight of 600 g., thus in the age groups VII-IX, was determined on almost 40 thousand grains of various sizes. Also describes in other studies: 27.5-115.5 thousand grains | 71.5 thousand eggs | Wajdowicz, 1974 |
20 | Absolute fecundity | In 1960, the fecundity of vimba in Kyzylagach bay was 8900-39600 eggs, average 27400 eggs. According to the data collected in 1963, the absolute fecundity of vimba of 13.5-20.5 cm varied from 8300 to 29200 eggs. The absolute fecundity of vimba from the Arakum waterbodies (central Caspian) was in the range of 7000-89200 eggs. The mean fecundity was: 25000 eggs in 1965, 23500 eggs in 1966, and 35200 eggs in 1967. Vimba in the Terek basin varied from 11900 to 65300 eggs. | 24250.0 thousand eggs | Kuliev, 1988 |
20 | Absolute fecundity | In eight females with mean SL=196.7 mm (188-213 mm) and mean weight 149.1 g (126-175 g), the absolute fecundity varied between 15,600 and 23,100 eggs (mean 19,300 eggs) | 200.5 thousand eggs | Lusk et al, 2005 |
20 | Absolute fecundity | The individual fecundity of the investigated Rega vimbs of the body lengths ranging within 25.0-38.0 cm amounts to 33800-139000 eggs (the mean value 77500), while its relative fecundity ranges from 81000 to 159000 eggs per 1 kg of fish (the mean value is 114600) [...] Other studies: With the body length range of 25.0-38.0 cm to vary from 40000 to 100000 eggs, the mean value being 66000 [...] Niemen vimbs within the range of 38000-130000 (the mean valu 73,600) | 31.5 thousand eggs | Trzebiatowski and Narozanski, 1973 |
20 | Absolute fecundity | A vimba can lay a total of 30,000-120,000 eggs in two or three batches. | 60.0 thousand eggs | Luszczek et al, 2008 |
21 | Oocyte development | Asynchonicity of oocyte maturation | Asynchronous | Hliwa et al, 2002 |
22 | Onset of oogenesis | October (already at stage III in November, in which they remained the entire winter | ['January', 'February', 'March', 'October', 'November'] | Shikhshabekov, 1979 |
22 | Onset of oogenesis | November | ['November'] | Hliwa et al, 2002 |
23 | Intensifying oogenesis activity | May | ['May'] | Hliwa et al, 2002 |
24 | Maximum GSI value | Mean 14.2%, but up to 18.0 [3 June] | 14.2 percent | Hliwa et al, 2002 |
24 | Maximum GSI value | The average weight of the gonads calculated from 10 specimens of V. vimba obtained in 1972, of body weight 550-750 g g., constitued about 13 to over 24 per cent of the body weight of the fish, the mean being 17.3 per cent | 650.0 percent | Wajdowicz, 1974 |
24 | Maximum GSI value | The mean GSI in eight examined females amounted to 13.9% (12.1-17.3%) | 14.7 percent | Lusk et al, 2005 |
26 | Resting period | 3 (June until August) | 3.0 months | Shikhshabekov, 1979 |
26 | Resting period | [July until October] | 5.0 months | Hliwa et al, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3 | 3.0 years | Shikhshabekov, 1979 |
27 | Age at sexual maturity | 2 | 2.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2 | 2.0 years | Coad, 2005 |
27 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 years | Keith and Allardi, 2001 |
27 | Age at sexual maturity | 3 [Unsexed] | 3.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | Vimba mature in the 2nd and 3rd year of life. The caspian vimba matures at the age of 3. Fish of age 2-5 participate in spawning, and 4-year-old fish are predominant in the spawning population. | 3.5 years | Kuliev, 1988 |
27 | Age at sexual maturity | Males become mature at the age 5. A common age of spawning vimba is 6-7 years | 6.5 years | Kesminas et al, 1999 |
27 | Age at sexual maturity | The youngest mature males in the spawning shoal in 1993 were four years old - 14 males and only one female (year class 1990). In 1995 seven mature males aged 3 years (year class 1992) and four mature females 4 years old (year class 1992) were found. Males generally matured one year-earlier than females. Analysis of the age structure of the spawning shoals sampled on 3 June, 1993 and 2 June, 1995 showed that they comprised mainly 4 to 6 year old fish, with a predominance in two year classes: four -and five -year old males comprising 91.97% of 83 individuals in 1993 and 82.30% of 96 individuals in 1995, whereas females consisted mainly of fishes in the age of five to six years in 1993 (=74.19% from 31 ind.) and four to six years in 1995 (=82.30% of 39 ind.) | 1993.0 years | Lusk et al, 2005 |
27 | Age at sexual maturity | The fourth age group almost exclusively comprised males, females being rarely encoutered. This indicates that males reach the maturity state in their fourth year of life, i.e., a year earlizer than females | 4.0 years | Trzebiatowski and Narozanski, 1973 |
28 | Length at sexual maturity | 15-31 | 23.0 cm | Shikhshabekov, 1979 |
28 | Length at sexual maturity | >20 | 20.0 cm | Bruslé and Quignard, 2001 |
28 | Length at sexual maturity | 13-19 | 16.0 cm | Coad, 2005 |
28 | Length at sexual maturity | The major part of the spawning population consists of 13-19 cm males. In all studied year, mature males ranges from 13.1-16.6 [Age 3]; 15.6-18.6 [Age 4], 17.3-20.1 [Age 5] | 16.0 cm | Kuliev, 1988 |
28 | Length at sexual maturity | Males migrating are 24.8-28.0 cm long | 26.4 cm | Kesminas et al, 1999 |
28 | Length at sexual maturity | 845 spawners with the body length (logitudo corporis) ranging from 24.5 to 40.5 cm and the total length (longitudo totalis) range of 29.5-48.5 cm | 39.0 cm | Trzebiatowski and Narozanski, 1973 |
29 | Weight at sexual maturity | 0.045-0.41 | 0.23 kg | Shikhshabekov, 1979 |
29 | Weight at sexual maturity | In all studied year, mature males ranges from 39-87 g [Age 3]; 60-124 [Age 4], 87-175 [Age 5] | 63.0 kg | Kuliev, 1988 |
30 | Male sexual dimorphism | A well-expressed spawning livery, the appearance of black stripes along the dorsal and ventral part of the body is usually observed in ripe males | Absent | Shikhshabekov, 1979 |
30 | Male sexual dimorphism | The males become black on the back, reddish on the belly, their fins become red and the tips of the dorsal and caudal fins become dark, and they develop minute tubercles on the body during the spawning season | Absent | Coad, 2005 |
30 | Male sexual dimorphism | Brighter colors of males, brown sides and red belly | Present | Billard, 1997 |
30 | Male sexual dimorphism | Take on mating colours, the dorsal part and sides becoming navy-blue and the fins and some ventral parts assuming and intensive colour. As a rule, after each migration, especially one connected with spawning, the runs swims back to the reservoir. | Absent | Wajdowicz, 1974 |
33 | Maximum GSI value | Mean GSI in 14 males was 2.48% (1.68-3.38%) | 2.53 percent | Lusk et al, 2005 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Anadromous migration: sometimes up to 870 km | 870.0 km | Bruslé and Quignard, 2001 |
36 | Spawning migration distance | Long migrations | No data | Keith and Allardi, 2001 |
36 | Spawning migration distance | Anadromous, but this population is stationary and non-migratory | No data | Hliwa and Martyniak, 2002 |
36 | Spawning migration distance | Semimigrating anadomic. For reproduction they migrate up the rivers. Migrating along the River Vistula, Vimba vimba reached even the River Raba about 800 km. Distant from the coast. Vimba vimba also develops local forms living only in fresh flowing waters, expecially in places where rivers have been artifically dammed. In these cases the existence of V. vimba in the dam reservoir is conditioned by the possibility of undertaking short spawning migrations to the non-damned part of the river as isthe case in natural conditions | 800.0 km | Wajdowicz, 1974 |
36 | Spawning migration distance | Until Kaunas hydroelectric power station was built, vimba used to migrate along the Nemunas to Stolbcai town (Belarus), which made 850 km from the river mouth. After Kaunas HPS dam was built and when transferring and marking of vimba reproducers was started, it was determined that the furthest distance of their migration reached 500 km, which was a bit shorter than before the dam building | 850.0 km | Kesminas et al, 1999 |
36 | Spawning migration distance | While migrating from the sea to the Trzebiatow spawning ground, the vimbs cover the distance of about 20 km | 20.0 km | Trzebiatowski and Narozanski, 1973 |
36 | Spawning migration distance | The fish engage in short-distance anadromous migration, moving to spawn upstream in barbel or grayling regions. | No data | Luszczek et al, 2008 |
37 | Spawning migration period | Exclusively in spring, in April-May at a temperature not lower than 10-12 | ['April', 'May', 'June'] | Shikhshabekov, 1979 |
37 | Spawning migration period | The spawning migration begins in March or April at 10-13°C | ['March', 'April'] | Coad, 2005 |
37 | Spawning migration period | The first migration, usually the most numerous, normally takes place in the middle of May, and the last one in the 1st, or less frequently in the 2nd decade of June | ['May', 'June'] | Wajdowicz, 1974 |
37 | Spawning migration period | At the beginning of the spawning migration in Kyzylagach Bay (March). At the and of march and beginning of April, the spawning migration of kutum and vobla is nearly finished, mass entry of vimba into the Malyy Kyzylagach is observed. In Dagestan waters, the most vimba enter the Terek, Sulak, samur rivers, and the Arakum waterbodies for spawning from April onward at water temperatres of 10-13°C/ mass-scale migration was recorded in the second half of May in water temperatures of 19-20°C | ['March', 'April', 'May'] | Kuliev, 1988 |
37 | Spawning migration period | The vimb spring migration is held in spring (April-May), a month before the spawning itself | ['April', 'May', 'June'] | Trzebiatowski and Narozanski, 1973 |
39 | Spawning season | First days of May | ['May'] | Shikhshabekov, 1979 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Billard, 1997 |
39 | Spawning season | April to June-July | ['April', 'May', 'June', 'July'] | Bruslé and Quignard, 2001 |
39 | Spawning season | End of April until the end of May or into June | ['April', 'May', 'June'] | Coad, 2005 |
39 | Spawning season | From Beginning of May until the first ten days of June | ['May', 'June'] | Hliwa and Martyniak, 2002 |
39 | Spawning season | End of April, Beginning of May, until end of May or End of June | ['April', 'May', 'June'] | Hliwa et al, 2002 |
39 | Spawning season | April and June | ['April', 'June'] | Keith and Allardi, 2001 |
39 | Spawning season | April to June | ['April', 'May', 'June'] | Fishbase, 2006 |
39 | Spawning season | May-July | ['May', 'July'] | Mann, 1996 |
39 | Spawning season | V. vimba span in the Zeller Ache, one of the main tributaries of Mondsee, at the end of May and beginning of June | ['May', 'June'] | Herzig and Winkler, 1986 |
39 | Spawning season | May-July | ['May', 'July'] | Maitland, 1977 |
39 | Spawning season | Spawns in Malyy Kyzylagach bay at the end of April and continues until the end of May | ['April', 'May'] | Kuliev, 1988 |
39 | Spawning season | May-June | ['May', 'June'] | Kamler and Wolnicki, 2006 |
39 | Spawning season | The vimb breeding in Rega usually takes place in late May or in the beginning of June | ['May', 'June'] | Trzebiatowski and Narozanski, 1973 |
39 | Spawning season | Between May and July | ['May', 'July'] | Luszczek et al, 2008 |
40 | Spawning period duration | 5 [But usually shorter] | 5.0 weeks | Hliwa and Martyniak, 2002 |
40 | Spawning period duration | 4 | 4.0 weeks | Hliwa et al, 2002 |
40 | Spawning period duration | Spawns in Malyy Kyzylagach bay at the end of April and continues until the end of May | No data | Kuliev, 1988 |
40 | Spawning period duration | The spawning of V. vimba in the studied locality occurred once each year according to our observations, and lasted 2-3 days; no other spawning sites were found in this part of the River Dyje. | 2.5 weeks | Lusk et al, 2005 |
41 | Spawning temperature | 16-17, mostly between 1-20 | 16.5 °C | Shikhshabekov, 1979 |
41 | Spawning temperature | 16-20°C | 18.0 °C | Coad, 2005 |
41 | Spawning temperature | 14-23 | 18.5 °C | Mann, 1996 |
41 | Spawning temperature | At temperatures ranging from 14°C to 18°C | 14.0 °C | Herzig and Winkler, 1986 |
41 | Spawning temperature | Water temperature of 17-18°C for the first spawning | 17.5 °C | Wajdowicz, 1974 |
41 | Spawning temperature | 18-20°C | 19.0 °C | Kuliev, 1988 |
41 | Spawning temperature | 14-18 | 16.0 °C | Kamler and Wolnicki, 2006 |
41 | Spawning temperature | Conditions during the spawning: 19.1-20°C [Somewhat cloudy, in 1-3 June 1993], 19.3-19.8 [Sunshine, 2-3 June 1994], 19.0-20.2°C [Overcast, 28-30 May 1995], 19.8 [Overcast, 1-2 June 1996], 20.2 [Somewaht cloudy, 3-4 June 1997] | 19.55 °C | Lusk et al, 2005 |
41 | Spawning temperature | The spawning itself begins most often in the early morning, when the water temperature is 16-18°C | 17.0 °C | Trzebiatowski and Narozanski, 1973 |
42 | Spawning water type | High rate flow : current of 0.6-0.9 m/second | Flowing or turbulent water | Shikhshabekov, 1979 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Current of 0.6-0.9 m/s | Flowing or turbulent water | Coad, 2005 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Maitland, 1977 |
42 | Spawning water type | Spawns in a swift current | Flowing or turbulent water | Wajdowicz, 1974 |
42 | Spawning water type | There is the largest number of vimba spawning grounds in this part of the river. For instance, one of the major factors, the average velocity of the flow in the Middle Nemunas fluctuates from 0.7 to 0.9 m/s and there are plenty of shallow gravelled segments of the riverbed there | Flowing or turbulent water | Kesminas et al, 1999 |
42 | Spawning water type | Favorable places for this fish are water bodies with weak current: bays, lakes, and reservoirs. | Stagnant water | Ermolin and Shashulovskii, 2006 |
42 | Spawning water type | For the spawning purposes the vimbs enter streams with clear water and fast current | Flowing or turbulent water | Trzebiatowski and Narozanski, 1973 |
42 | Spawning water type | Fast-flowing river currents, in well oxygenated waters | Flowing or turbulent water | Luszczek et al, 2008 |
43 | Spawning depth | Shallow | No data | Maitland, 1977 |
43 | Spawning depth | Shallow gravelled segments of the riverbed there | No data | Kesminas et al, 1999 |
44 | Spawning substrate | Gravel or stones | Lithophils | Shikhshabekov, 1979 |
44 | Spawning substrate | Lithophil : pebbles [Rarely on aquatic plants when there is flood] | Lithophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Eggs are deposited on gravel or stones, concrete structures and flooded fields | Lithophils | Coad, 2005 |
44 | Spawning substrate | Gravels | Lithophils | Billard, 1997 |
44 | Spawning substrate | Gravels, or plants | Lithophils | Keith and Allardi, 2001 |
44 | Spawning substrate | Stones and gravel, flooded grasses | Lithophils | Mann, 1996 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Generatively lithophilous. Use for spawning the stony-gravelled bottom parts of the River Czarna orawa above the reservoir | Lithophils | Wajdowicz, 1974 |
44 | Spawning substrate | Gravelled segments of the riverbed | Lithophils | Kesminas et al, 1999 |
44 | Spawning substrate | Its belong sto the lithophilous group | Lithophils | Ermolin and Shashulovskii, 2006 |
44 | Spawning substrate | Deposit eggs on stony and gravel beds | Lithophils | Trzebiatowski and Narozanski, 1973 |
44 | Spawning substrate | On a gravel bottom covered with pebbles or larger stones | Lithophils | Luszczek et al, 2008 |
45 | Spawning site preparation | Open water/substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawners | Open water/substratum scatter | Mann, 1996 |
45 | Spawning site preparation | Female lays their eggs on substrate | Susbtrate chooser | Keith and Allardi, 2001 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
46 | Nycthemeral period of oviposition | The spawning itself begins most often in the early morning | Day | Trzebiatowski and Narozanski, 1973 |
47 | Mating system | The spawning behaviour and the course of spanwing was similar to those of the nase carp Chondrostoma nasus. The spawning ground was occupied by the shoal consisting of males, whereas females stayed downstream of the place. Ripe females came individually to the spawning site where the group of males joined them. The whole group of one female and several males moved upstream with simultaneous releasing of gametes. Males were found only sporadically away from the spawning place | Polyandry | Lusk et al, 2005 |
47 | Mating system | The spawners gathered in the spawing site form groups consisting of several individuals, one female being always accompanied by a few males […] The spawning as a rule is very boisterous, accompanied by the water splash, vigorous swimming and movements of fishes | Promiscuity | Trzebiatowski and Narozanski, 1973 |
48 | Spawning release | Spawning is non-intermittent, however it could also spawn intermittently (as many as 3 batches of eggs with interval of 14-15 days) | Multiple | Shikhshabekov, 1979 |
48 | Spawning release | Spawning is non-intermittent | Fractional | Coad, 2005 |
48 | Spawning release | Usually spawn twice in one season, or even three times | No category | Hliwa and Martyniak, 2002 |
48 | Spawning release | Three batches | Multiple | Hliwa et al, 2002 |
48 | Spawning release | As a portion-spawning fish, V. vimba usually makes, with favourable weather conditions, 2-3 spawning migrations from this reservoir | No category | Wajdowicz, 1974 |
48 | Spawning release | Ovaries, close to the spawning, contain small (24-45%) and large (55-75%) eggs, which indicates spawning in batches | Multiple | Kuliev, 1988 |
48 | Spawning release | According to our examination wimba has a single spawning per season in the studied population. According to other study, V. vimba in the basins of the Baltic and Black seas is a repeat spawner (2-3 batches) and it is therefore impossible to compare those results with ours | Multiple | Lusk et al, 2005 |
48 | Spawning release | Batch spawning | Multiple | Luszczek et al, 2008 |
49 | Parity | Life span is 6 years in Iran, at least 7 years elsewhere | No category | Coad, 2005 |
49 | Parity | At least six age class, from 4+ to 9+ participate in the spawning season | No category | Hliwa and Martyniak, 2002 |
49 | Parity | Mature females range from 5+ to 9+ | No category | Hliwa et al, 2002 |
49 | Parity | Soon after spawning, the spawners migrate toward river mouths, where they feed until the next spawning season | No category | Kuliev, 1988 |
49 | Parity | The oldest individual found in our study was a female of 10 years and 300 mm Sl. One aged 9 years and three aged 8 years were also females. The oldest males (n=6) were 7 years old and there were 8 females of this age | No category | Lusk et al, 2005 |
50 | Parental care | No protection, after spawning the vimba does not stay in the spawning grounds | No care | Shikhshabekov, 1979 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |
50 | Parental care | Soon after spawning, the spawners migrate toward river mouths, where they feed until the next spawning season | No category | Kuliev, 1988 |