Trait completeness | 60% |
Total data | 75 |
References | 10 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.75-2.2 [Not specified] | 1.98 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.5-1.7 [South-west of France], 1.8-2.2 [South-east of France] | 1.6 mm | Gozlan and Chappaz, 2001 |
1 | Oocyte diameter | 2.00 [Average diameter of the largest oocyte in fully developed ovaries] | 2.0 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | About 2 [Not specified] | 2.0 mm | Bensettiti and Gaudillat, 2002 |
2 | Egg size after water-hardening | Mean 2.1, range 1.9-2.5 [After activation] | 2.2 mm | Gozlan et al, 1999 |
2 | Egg size after water-hardening | About 2 mm [Not specified] | 2.0 mm | Internet |
3 | Egg Buoyancy | Demersal [eggs are deposited on boulders in deep pools] | Demersal | Gozlan et al, 1999 |
4 | Egg adhesiveness | Becoming adhesive | Adhesive | Gozlan et al, 1999 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
5 | Incubation time | 12-15 | 13.5 days | Spillmann, 1961 |
5 | Incubation time | 8 days at 15-18.5°C | 16.75 days | Gozlan et al, 1999 |
6 | Temperature for incubation | 15-18.5 | 16.75 °C | Gozlan et al, 1999 |
7 | Degree-days for incubation | 120-150 | 135.0 °C * day | Gozlan et al, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | Mean 6.32, range 4.1-8.1 | 6.1 mm | Gozlan et al, 1999 |
9 | Larvae behaviour | Benthic larvae [The free embryos laid more or less on the bottom of the tank, but from time to time darted horizontally. Then, they fell back to the bottom and rest passively for some time.] | Demersal | Gozlan et al, 1999 |
10 | Reaction to light | The free-embryos developed early photophobia and tended to congregate | Photopositive | Gozlan et al, 1999 |
10 | Reaction to light | Initially the larvae are photophobic | Photophobic | Mann, 1996 |
11 | Temperature during larval development | 16-19 | 17.5 °C | Gozlan et al, 1999 |
12 | Sibling intracohort cannibalism | No cannibalism or aggressive behaviour was observed | Absent | Gozlan et al, 1999 |
14 | Onset of exogeneous feeding | 180 [10 days and 20 hour at 16-17] à vérifier | 16.5 °C * day | Gozlan et al, 1999 |
14 | Onset of exogeneous feeding | 70-80 [4 days at 16-18°C] | 75.0 °C * day | Pinder and Gozlan, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4 | 4.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 year | Gozlan and Chappaz, 2001 |
15 | Age at sexual maturity | 4 [48 months, age at maturation] | 4.0 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 4 [Not specified] | 4.0 year | Bensettiti and Gaudillat, 2002 |
15 | Age at sexual maturity | At four years inVerdon (France), sex not specified | 4.0 year | Internet |
16 | Length at sexual maturity | 11-12 [South-west of France], 18-20 [South-east of France] | 11.5 cm | Gozlan and Chappaz, 2001 |
18 | Female sexual dimorphism | Does not seem to present any sexual dimorphims | Present | Internet |
20 | Absolute fecundity | 2.3-3.5 | 2.9 thousand eggs | Spillmann, 1961 |
20 | Absolute fecundity | 7-15 | 11.0 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 1.5-15 | 8.25 thousand eggs | Gozlan and Chappaz, 2001 |
20 | Absolute fecundity | 3.2 [Average number of vitellogenic oocyes of mature females in a single spawning season] | 3.2 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
20 | Absolute fecundity | 11.5 | 11.5 thousand eggs | Bensettiti and Gaudillat, 2002 |
20 | Absolute fecundity | A female can spawn 11 500 eggs | 11.0 thousand eggs | Internet |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 years | Gozlan and Chappaz, 2001 |
28 | Length at sexual maturity | 11-12 [South-west of France], 18-20 [South-east of France] | 11.5 cm | Gozlan and Chappaz, 2001 |
30 | Male sexual dimorphism | Do not seem to display any bright color | Present | Spillmann, 1961 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
39 | Spawning season | April | ['April'] | Billard, 1997 |
39 | Spawning season | April | ['April'] | Bruslé and Quignard, 2001 |
39 | Spawning season | April | ['April'] | Spillmann, 1961 |
39 | Spawning season | End of May, beginning of July [30 or 40 days after Hotu] | ['May', 'July'] | Gozlan and Chappaz, 2001 |
39 | Spawning season | March to May, up to June | ['March', 'April', 'May', 'June'] | Bensettiti and Gaudillat, 2002 |
39 | Spawning season | From March to May, and upto June | ['March', 'April', 'May', 'June'] | Internet |
40 | Spawning period duration | 4 [1.00 month, length of breeding season] | 4.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
41 | Spawning temperature | 13 | 13.0 °C | Spillmann, 1961 |
41 | Spawning temperature | 9-11 | 10.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 11-13 [South-est of France], 15-16 [South-west of France] | 12.0 °C | Gozlan and Chappaz, 2001 |
41 | Spawning temperature | 11-13 | 12.0 °C | Bensettiti and Gaudillat, 2002 |
41 | Spawning temperature | 11-13 | 12.0 °C | Internet |
42 | Spawning water type | Water with current | Flowing or turbulent water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Small rivers or near the shore of main stream | Stagnant water | Gozlan and Chappaz, 2001 |
42 | Spawning water type | Small tributary streams, deep pools just dowstream of riffles | No category | Gozlan et al, 1999 |
42 | Spawning water type | Small rivers with strong current | Flowing or turbulent water | Bensettiti and Gaudillat, 2002 |
42 | Spawning water type | Search for small tributaries with strong current | Flowing or turbulent water | Internet |
43 | Spawning depth | Very shallow waters | No data | Billard, 1997 |
43 | Spawning depth | Deep pools | No data | Gozlan et al, 1999 |
43 | Spawning depth | Shallow water | No data | Bensettiti and Gaudillat, 2002 |
43 | Spawning depth | Shallow water | No data | Internet |
44 | Spawning substrate | Gravels | Lithophils | Billard, 1997 |
44 | Spawning substrate | Gravels | Lithophils | Gozlan and Chappaz, 2001 |
44 | Spawning substrate | Boulders | No category | Gozlan et al, 1999 |
44 | Spawning substrate | Stones and gravel | Lithophils | Mann, 1996 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Coarse gravel | Lithophils | Bensettiti and Gaudillat, 2002 |
44 | Spawning substrate | Coarse substrate | No category | Internet |
45 | Spawning site preparation | No, eggs are deposited on boulders in deep pools | Susbtrate chooser | Gozlan et al, 1999 |
45 | Spawning site preparation | Zygotes are placed in a special habitat (e.g. scattered on vegetation, or buried in gravel) | Susbtrate chooser | Vila-Gispert and Moreno-Amich, 2002 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
45 | Spawning site preparation | Eggs are deposited on the substrate | Susbtrate chooser | Bensettiti and Gaudillat, 2002 |
48 | Spawning release | Single spawning per year | Total | Vila-Gispert and Moreno-Amich, 2002 |
49 | Parity | Single spawning per year | Iteroparous | Vila-Gispert and Moreno-Amich, 2002 |
49 | Parity | Could live up to 9 years | No category | Bensettiti and Gaudillat, 2002 |
49 | Parity | Could live up to 9 years | No category | Internet |
50 | Parental care | Nonguarding | No care | Gozlan et al, 1999 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |