Trait completeness | 86% |
Total data | 123 |
References | 21 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.7 | 1.7 mm | Coad, 2005 |
2 | Egg size after water-hardening | 2.0-2.2 [Up to 2.4] | 2.1 mm | Coad, 2005 |
2 | Egg size after water-hardening | 1.9-2.1 [Seems to be fertilized eggs] | 2.0 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | 2.0 [Not specified] | 2.0 mm | Kamler and Wolnicki, 2006 |
3 | Egg Buoyancy | Demersal | Demersal | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Adhering to stone | Adhesive | Coad, 2005 |
4 | Egg adhesiveness | Adhesive | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Adhesive [Stick to gravels or immerged plants] | Adhesive | Keith and Allardi, 2001 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | Stick to stones or plants | Adhesive | Bensettiti and Gaudillat, 2002 |
5 | Incubation time | 9-10 | 9.5 days | Coad, 2005 |
5 | Incubation time | 10-15 at 12-16°C | 12.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 10-17 | 13.5 days | Keith and Allardi, 2001 |
5 | Incubation time | 10-17 | 13.5 days | Bensettiti and Gaudillat, 2002 |
6 | Temperature for incubation | 12-16 | 14.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | In experimental conditions, best results were obtained between 7-17.2°C, and the best at 12.8°C | 12.1 °C | Bensettiti and Gaudillat, 2002 |
6 | Temperature for incubation | Viable range 7-17, threshold temperature at which ontogeny is theoretically arrested: 6.8 | 12.0 °C | Kamler and Wolnicki, 2006 |
6 | Temperature for incubation | Fertilized eggs were incubated at constant temperature of 14°C | 14.0 °C | Kujawa et al, 2007 |
7 | Degree-days for incubation | 160-180 [10-15 at 12-16°C] | 170.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 74 [Effective day-degrees] | 74.0 °C * day | Kamler, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 4-6 | 5.0 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | On the first day post-hatch, the asp larvae measured 6.2 in mean total length | 6.2 mm | Ostaszewska, 2002 |
8 | Initial larval size | Length range mean 8.9 (range 7.9-9.3 mm), at day 1 | 8.6 mm | Kujawa et al, 2007 |
10 | Reaction to light | Initially the larvae are photophobic | Photophobic | Mann, 1996 |
10 | Reaction to light | The photoperiod was 18 h light and 6 h dark | Photopositive | Kujawa et al, 2007 |
11 | Temperature during larval development | Reared at 25-26°C | 25.5 °C | Kamler and Wolnicki, 2006 |
11 | Temperature during larval development | Optimum temperatures for larval growth (expressed as Relative growth rate: RGR, %d): 22-28°C | 25.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | The larvae were allowed to develop at 18-20°C | 19.0 °C | Ostaszewska, 2002 |
11 | Temperature during larval development | Rearing temperature ranged from 14 and 18.7°C (mean 17.2°C) | 14.0 °C | Kujawa et al, 2007 |
13 | Full yolk-sac resorption | On day 11, when the larvae averaged 10.17 mm, the yolk sac was completely resorbed and the period of exogenous feeding begin (at 18-20°C) | 19.0 °C * day | Ostaszewska, 2002 |
13 | Full yolk-sac resorption | The yolk sac was completely absorbed on day 11 post hatch | 11.0 °C * day | Ostaszewska and Wegiel, 2002 |
14 | Onset of exogeneous feeding | First-feeding larvae age 6 days post-hatching at 20°C, Lt 7.8 ± 0.6 mm, body weight 2.7 ±0.2 mg | 7.8 °C * day | Wolnicki, 2005 |
14 | Onset of exogeneous feeding | From hatch until day 3, the larvae obtain nutrition from susbtances stored in the yolk sac. Between day 3 and 11, the larvae started endo-exogenous feeding. | 3.0 °C * day | Ostaszewska, 2002 |
14 | Onset of exogeneous feeding | Between days 3 and 5 post hatch, the intestine opened at both ends and lined with columnar epithelium. Signs of digestion and lipid absorption by enterocytes were observed on day 5, while protein absorption started on day 7 of the larval development. | 3.0 °C * day | Ostaszewska and Wegiel, 2002 |
14 | Onset of exogeneous feeding | Beginning of exogenous (mixed) feeding at 7 days at 14°C | 7.0 °C * day | Kujawa et al, 2007 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4 | 4.0 year | Shikhshabekov, 1979 |
15 | Age at sexual maturity | 4-5 [Danube] | 4.5 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3-5 [Sex not specified] | 4.0 year | Keith and Allardi, 2001 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Kompowski et Neja, 2004 |
15 | Age at sexual maturity | About 4 [Sex not specified] | 4.0 year | Bensettiti and Gaudillat, 2002 |
16 | Length at sexual maturity | 41-58 | 49.5 cm | Shikhshabekov, 1979 |
16 | Length at sexual maturity | 37.32-45.47 [Female] | 41.39 cm | Kompowski et Neja, 2004 |
17 | Weight at sexual maturity | 0.840-2.800 | 1.82 kg | Shikhshabekov, 1979 |
18 | Female sexual dimorphism | Sex was not determined, as this was impossible without harming the fish, especially in the post-spawing season | Absent | Fredrich, 2003 |
19 | Relative fecundity | 63-67 | 65.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | Mean 70.53 ± 13.20, range 35.11 to 107.94 | 70.53 thousand eggs/kg | Kompowski et Neja, 2004 |
20 | Absolute fecundity | 52-212 | 132.0 thousand eggs | Shikhshabekov, 1979 |
20 | Absolute fecundity | 80-100 | 90.0 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 80-1000 | 540.0 thousand eggs | Keith and Allardi, 2001 |
20 | Absolute fecundity | Mean of 158.526 ± 56.659 [Range 63,044 in females 43.3 cm in length and 324,833 in female 64.3 cm length] [Absolute fecundities in other populations: 16-269; 48.3-121.9; 52.2-212.8; 67.6-189.0; 73.5-366.5; 63-324.8] | 158.53 thousand eggs | Kompowski et Neja, 2004 |
20 | Absolute fecundity | 58-500 | 279.0 thousand eggs | Bensettiti and Gaudillat, 2002 |
22 | Onset of oogenesis | Beginning of September and continue to increase regularly in the winter period (December-February) | ['January', 'February', 'March', 'September', 'December'] | Shikhshabekov, 1979 |
22 | Onset of oogenesis | During the fall from September to November, the average GSI value rose sharply to a level close to that seen in the pre-spawning period | ['September', 'October', 'November', 'December'] | Kompowski et Neja, 2004 |
22 | Onset of oogenesis | The maturation of gonads is synchronous and complete in the previous autumn | ['October', 'November', 'December'] | Fredrich et al, 2003 |
23 | Intensifying oogenesis activity | March-April | ['March', 'April'] | Shikhshabekov, 1979 |
24 | Maximum GSI value | The highest average values of this index among females 12.07 occurred at the end of March. This is also when the maximum individual value of this index was observed 20.73 (range 0.22-20.73) | 10.47 percent | Kompowski et Neja, 2004 |
24 | Maximum GSI value | 8.6-15.3 (mean 11.6) | 11.95 percent | Shikhshabekov, 1979 |
26 | Resting period | 3-3.5 [Between Mid-May until end of August] | 3.25 months | Shikhshabekov, 1979 |
26 | Resting period | 1.61 [Between May to August] | 1.61 months | Kompowski et Neja, 2004 |
26 | Resting period | 1.1 | 1.1 months | Shikhshabekov, 1979 |
26 | Resting period | In April, the average female GSI fell to 1.77, which indicates that the majority of the studied fish had already spawned. In May the female GSI value was even lower at 1.04. During the fall from September to November, the average GSI value rose sharply to a level close to that seen in the pre-spawning period. | 1.77 months | Kompowski et Neja, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 4 | 4.0 years | Shikhshabekov, 1979 |
27 | Age at sexual maturity | 3-4 | 3.5 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 4-5 [Male], only only one at 3 | 4.5 years | Kompowski et Neja, 2004 |
28 | Length at sexual maturity | 41-58 | 49.5 cm | Shikhshabekov, 1979 |
28 | Length at sexual maturity | 39.20-45.09 [Male] | 42.15 cm | Kompowski et Neja, 2004 |
29 | Weight at sexual maturity | 0.840-2.800 | 1.82 kg | Shikhshabekov, 1979 |
30 | Male sexual dimorphism | Male bears nuptial tubercles over the body, particulalry the head during the breeding season | Present | Billard, 1997 |
30 | Male sexual dimorphism | Male bears nuptial tubercles | Present | Keith and Allardi, 2001 |
31 | Onset of spermatogenesis | September-October | ['September', 'October'] | Kompowski et Neja, 2004 |
32 | Main spermatogenesis activity | December to March | ['January', 'February', 'March', 'December'] | Kompowski et Neja, 2004 |
33 | Maximum GSI value | 2.02 [April] | 2.02 percent | Kompowski et Neja, 2004 |
34 | Spermatogenesis duration | From September to April | 8.0 months | Kompowski et Neja, 2004 |
35 | Resting period | 0.14 [August] | 2.0 months | Kompowski et Neja, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Anadromous migrations, short | No data | Bruslé and Quignard, 2001 |
36 | Spawning migration distance | The migratory behaviour of asp was highly variable; 34 asp observed for more than 1 year lived in home ranges of 1 to > 100 stream kilometres mostly near their capture site. Longest observed migratrion from summer habitat in the Tidal Elbe back to the spawning ground in the middle of Elbe was 166 skm [To date, long upstream migrations (>50 km) from the lower river section are seldom observed] | 50.0 km | Fredrich, 2003 |
36 | Spawning migration distance | Anadromos migrations in shoals | No data | Bensettiti and Gaudillat, 2002 |
37 | Spawning migration period | Emerges from the overwintering habitat in early spring at the time of the onset of floods | ['January', 'February', 'March', 'April', 'May', 'June'] | Shikhshabekov, 1979 |
37 | Spawning migration period | The first cyprinid migrating to the tributary to spawn each year was asp. 1 March to approximatively 10 April, asp dominates in biomass and sometimes in numbers. Prespawning migration of perch, roach and bream is also apparent. | ['March', 'April'] | Hladik and Kubecka, 2003 |
38 | Homing | Tendendy to return to the same spawning ground (reproductive homing) | Present | Fredrich et al, 2003 |
39 | Spawning season | April-June | ['April', 'June'] | Billard, 1997 |
39 | Spawning season | Mid-February to late March | ['February', 'March'] | Coad, 2005 |
39 | Spawning season | April-May and beginning June | ['April', 'May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | April to June | ['April', 'May', 'June'] | Keith and Allardi, 2001 |
39 | Spawning season | April-May | ['April', 'May'] | Mann, 1996 |
39 | Spawning season | First half of April in Polish part and as earlt as March in German part | ['March', 'April'] | Kompowski et Neja, 2004 |
39 | Spawning season | Late March/April | ['March', 'April'] | Fredrich, 2003 |
39 | Spawning season | April to June, according to the latitude | ['April', 'May', 'June'] | Bensettiti and Gaudillat, 2002 |
39 | Spawning season | Late winter or early spring | ['January', 'February', 'March', 'April', 'May', 'June'] | Fredrich et al, 2003 |
39 | Spawning season | March-May | ['March', 'May'] | Kamler and Wolnicki, 2006 |
40 | Spawning period duration | 1-2 (short) | 1.5 weeks | Shikhshabekov, 1979 |
40 | Spawning period duration | Short | No data | Bruslé and Quignard, 2001 |
40 | Spawning period duration | 1-2 [10-15 days] | 1.5 weeks | Coad, 2005 |
41 | Spawning temperature | 8-10 | 9.0 °C | Shikhshabekov, 1979 |
41 | Spawning temperature | Start with 4-6°C | 5.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 17-28 | 22.5 °C | Mann, 1996 |
41 | Spawning temperature | The average water temperature in the river during asp spawning reached 7-8°C | 7.5 °C | Hladik and Kubecka, 2003 |
41 | Spawning temperature | 5-12 | 8.5 °C | Kamler and Wolnicki, 2006 |
42 | Spawning water type | Open sections of the lake with the greatest flow, more rarely in places weaklt overgrown with very coarse submerged vegetation (mainly reeds and rushes) | Stagnant water | Shikhshabekov, 1979 |
42 | Spawning water type | After riffles | No category | Bruslé and Quignard, 2001 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Billard, 1997 |
42 | Spawning water type | Water with strong current | Flowing or turbulent water | Keith and Allardi, 2001 |
42 | Spawning water type | Water with strong current | Flowing or turbulent water | Bensettiti and Gaudillat, 2002 |
42 | Spawning water type | Some species seem to be strickly dependent on the tributary zone as they were never observed reproducing in the reservoir (asp, bleak, chub and white bream), while others are facultative tributary users (roach, bream, pike, perch, rudd). | No category | Hladik and Kubecka, 2003 |
44 | Spawning substrate | Lithophil : stones and gravels | Lithophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Over grounds with stones, gravels and coarse sand | Lithophils | Billard, 1997 |
44 | Spawning substrate | Gravel | Lithophils | Keith and Allardi, 2001 |
44 | Spawning substrate | Gravel/ large boulders | Lithophils | Mann, 1996 |
44 | Spawning substrate | Lithophil | Lithophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Gravels | Lithophils | Bensettiti and Gaudillat, 2002 |
45 | Spawning site preparation | Open susbstratum spawners | No category | Mann, 1996 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
48 | Spawning release | Spawning is non-intermittent | Fractional | Shikhshabekov, 1979 |
48 | Spawning release | Eggs are released synchronously | No category | Bruslé and Quignard, 2001 |
48 | Spawning release | Spawn once a year | Total | Fredrich et al, 2003 |
48 | Spawning release | Asp has only one spawning | No category | Hladik and Kubecka, 2003 |
49 | Parity | Life span in the Volga delta is 7-8 years with the bulk of the population mature at 6 years. In the waters of Dagestan life span is 8 years with maturity at 4 years | No category | Coad, 2005 |
49 | Parity | The representatives of every age class within the range of 3-16 years were found in the material studied | Semelparous | Trzebiatowski and Leszcewicz, 1976 |
49 | Parity | Females migrated to the tributary later and returned immediatly after spawning. Males seem to stay at the spawning grounds a few days longer | No category | Hladik and Kubecka, 2003 |
50 | Parental care | No, immediatly after spawning the asp leaves the spawning ground for the sea | No care | Shikhshabekov, 1979 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |
50 | Parental care | Asp return quickly to the reservoir and evn its juveniles do not stay in the river for long | No care | Hladik and Kubecka, 2003 |