Trait completeness | 60% |
Total data | 68 |
References | 9 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 0.8-1.2 [Ovules with the larger diameter in ova] | 1.0 mm | Vargas and De Sostoa, 1997 |
1 | Oocyte diameter | Big eggs | No data | Billard, 1997 |
1 | Oocyte diameter | Big eggs | No data | Keith, 2001 |
1 | Oocyte diameter | 1.20 [Average diameter of the largest oocyte in fully developed ovaries] | 1.2 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | Mean egg diameter of 0.7285 for age 1 and 0.8145 for age 0 | 0.73 mm | Fernandez-Delgado et al, 1988 |
3 | Egg Buoyancy | Demersal [Eggs are deposited on plants located on the ground] | Demersal | Billard, 1997 |
5 | Incubation time | 8-10 | 9.0 days | Keith, 2001 |
5 | Incubation time | 10-15 | 12.5 days | Maitland, 1977 |
Trait id | Trait | Primary Data | Secondary Data | References |
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Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1 [Sex not precised] | 1.0 year | Keith, 2001 |
15 | Age at sexual maturity | Before 1 [Both sex] | 1.0 year | Vargas and De Sostoa, 1997 |
15 | Age at sexual maturity | 0.4 [4 months, age at maturation] | 0.4 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 1 [Not specified] | 1.0 year | Maitland, 1977 |
15 | Age at sexual maturity | From April to July, 1+ group specimens (7-12 months old) reproduced. Their offspring (0+ group; 3-4 months) reproduced) from July to September. | 9.5 year | Fernandez-Delgado et al, 1988 |
16 | Length at sexual maturity | From 2.3 to 2.8 [Females] | 2.3 cm | Fernandez-Delgado et al, 1988 |
18 | Female sexual dimorphism | Males mature before famles, but females were larger than males | Absent | Fernandez-Delgado et al, 1988 |
19 | Relative fecundity | F=8.358 x 10-9 x Lt6.343 [with L < 45 mm] | 9.5 thousand eggs/kg | Vargas and De Sostoa, 1997 |
19 | Relative fecundity | 1609.76 [For age 1] and 759.07 [for Age 0] | 1609.76 thousand eggs/kg | Fernandez-Delgado et al, 1988 |
20 | Absolute fecundity | 0.438 [Average number of vitellogenic oocyes of mature females in a single spawning season] | 0.44 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
21 | Oocyte development | The ovules displayed continuous, rapid development, in small groups | No category | Vargas and De Sostoa, 1997 |
22 | Onset of oogenesis | March-April | ['March', 'April'] | Vargas and De Sostoa, 1997 |
22 | Onset of oogenesis | January-February | ['January', 'February'] | Fernandez-Delgado et al, 1988 |
23 | Intensifying oogenesis activity | April and June [Decreased in June, certainly due to the first fractioned spawning at the end of May] | ['April', 'May', 'June'] | Vargas and De Sostoa, 1997 |
23 | Intensifying oogenesis activity | March-April | ['March', 'April'] | Fernandez-Delgado et al, 1988 |
24 | Maximum GSI value | Mean of 14 [Up to 17.5] in July | 14.0 percent | Vargas and De Sostoa, 1997 |
24 | Maximum GSI value | Two maxima: one in April [mean of 13, up to 14.5] and a second in August-September [mean of 3, up to 4]. Each maximum represented females of different ages | 13.0 percent | Fernandez-Delgado et al, 1988 |
25 | Oogenesis duration | From March to May-June | 5.0 months | Vargas and De Sostoa, 1997 |
26 | Resting period | From September to February | 6.0 months | Vargas and De Sostoa, 1997 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1 [Sex not precised] | 1.0 years | Keith, 2001 |
27 | Age at sexual maturity | Before 1 [Both sex] | 1.0 years | Vargas and De Sostoa, 1997 |
27 | Age at sexual maturity | From April to July, 1+ group specimens (7-12 months old) reproduced. Their offspring (0+ group; 3-4 months) reproduced) from July to September. | 9.5 years | Fernandez-Delgado et al, 1988 |
28 | Length at sexual maturity | Between 1.7 to 2.4 [Male] | 1.7 cm | Fernandez-Delgado et al, 1988 |
31 | Onset of spermatogenesis | March-April [Beginning of gonadal activity] | ['March', 'April'] | Vargas and De Sostoa, 1997 |
31 | Onset of spermatogenesis | Gonad development started in February and continued till April | ['February', 'April'] | Fernandez-Delgado et al, 1988 |
32 | Main spermatogenesis activity | April-May | ['April', 'May'] | Vargas and De Sostoa, 1997 |
32 | Main spermatogenesis activity | March-April | ['March', 'April'] | Fernandez-Delgado et al, 1988 |
33 | Maximum GSI value | Mean of 2.0 [Up to 2.6], in May | 2.0 percent | Vargas and De Sostoa, 1997 |
33 | Maximum GSI value | Mean of 0.5 [In April] | 0.5 percent | Fernandez-Delgado et al, 1988 |
34 | Spermatogenesis duration | From September until January | 5.0 months | Fernandez-Delgado et al, 1988 |
35 | Resting period | A period of repose from September to February | 6.0 months | Vargas and De Sostoa, 1997 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
39 | Spawning season | Summer | ['July', 'August', 'September'] | Billard, 1997 |
39 | Spawning season | April-August | ['April', 'August'] | Keith, 2001 |
39 | Spawning season | May to August | ['May', 'June', 'July', 'August'] | Oltra and Todoli, 2000 |
39 | Spawning season | May to August | ['May', 'June', 'July', 'August'] | Vargas and De Sostoa, 1997 |
39 | Spawning season | July-August | ['July', 'August'] | Fishbase, 2006 |
39 | Spawning season | April-August | ['April', 'August'] | Maitland, 1977 |
39 | Spawning season | May to September | ['May', 'June', 'July', 'August', 'September'] | Fernandez-Delgado et al, 1988 |
40 | Spawning period duration | 14-16 [From May to August] | 15.0 weeks | Vargas and De Sostoa, 1997 |
40 | Spawning period duration | 16 [4.00 months, length of breeding season] | 16.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
41 | Spawning temperature | 25 | 25.0 °C | Billard, 1997 |
41 | Spawning temperature | 22-24 [In aquaria] | 23.0 °C | Oltra and Todoli, 2000 |
43 | Spawning depth | Shallow waters | No data | Keith, 2001 |
43 | Spawning depth | Shallow waters | No data | Maitland, 1977 |
44 | Spawning substrate | Within aquatic plants | Phytophils | Keith, 2001 |
44 | Spawning substrate | Natural plants | Phytophils | Oltra and Todoli, 2000 |
44 | Spawning substrate | Phytophils | Phytophils | Balon, 1975 |
44 | Spawning substrate | Within aquatic plants | Phytophils | Maitland, 1977 |
45 | Spawning site preparation | Eggs are deposited on plants located on the ground | Susbtrate chooser | Billard, 1997 |
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 water / substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
48 | Spawning release | Multiple spawning throughout the reproductive cycle | Multiple | Vargas and De Sostoa, 1997 |
48 | Spawning release | Batches of 10 to 30 eggs | Multiple | Vargas and De Sostoa, 1997 |
48 | Spawning release | More than four spawning per year | No category | Vila-Gispert and Moreno-Amich, 2002 |
48 | Spawning release | Multiple spawner | Multiple | Fernandez-Delgado et al, 1988 |
49 | Parity | Only few male and female adults of the 1+ group succeed in surviving the reproductive phase and the following winter | No category | Vargas and De Sostoa, 1997 |
49 | Parity | This stock contains only three age groups (0+, 1+, and 2 +) of which 0+ group constitutes more than 95% [Very few of the 1+ group specimens survived to spawn the following year] | No category | Fernandez-Delgado et al, 1988 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |