Trait completeness | 56% |
Total data | 37 |
References | 6 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.278 ± 0.016 [Egg within the gonad]± | 1.28 mm | Oliva-Paterna et al, 2002 |
1 | Oocyte diameter | 1.00 [Average diameter of the largest oocyte in fully developed ovaries] | 1.0 mm | Vila-Gispert and Moreno-Amich, 2002 |
2 | Egg size after water-hardening | Diameter of the chorion, mean 1.71 ± 0.08, range 1.53-1.86 | 1.71 mm | Bohlen, 2000 |
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 | Beginning of 2 year [Both sex specified] | 2.0 year | Oliva-Paterna et al, 2002 |
15 | Age at sexual maturity | 2-3 [Most at 3, but some as 1, female] | 2.5 year | Soriguer et al, 2000 |
15 | Age at sexual maturity | 1 [12 months, age at maturation] | 1.0 year | Vila-Gispert and Moreno-Amich, 2002 |
16 | Length at sexual maturity | 5.8-6.4 | 6.1 cm | Oliva-Paterna et al, 2002 |
18 | Female sexual dimorphism | A change of coloration is observed only during spawning activity: the female became very intensely pigmented [This spawning coloration. This spawning coloration disappeared within a few hours after spawning activity | Absent | Bohlen, 2000 |
20 | Absolute fecundity | 1.235-1.986 The last for a female of 90 mm] | 1.61 thousand eggs | Oliva-Paterna et al, 2002 |
20 | Absolute fecundity | 1.100 [Average number of vitellogenic oocyes of mature females in a single spawning season] | 1.1 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
20 | Absolute fecundity | 0.4-1.1, up to 1.4 | 0.75 thousand eggs | Perdices and Doadrio, 1977 |
21 | Oocyte development | Asynchornous, with oocytes in different stages of vitellogenesis, three maturation of yolky eggs in the population were detected | Asynchronous | Oliva-Paterna et al, 2002 |
22 | Onset of oogenesis | December-January | ['January', 'December'] | Oliva-Paterna et al, 2002 |
23 | Intensifying oogenesis activity | Greatest increase in Late March-Early April | ['March', 'April'] | Oliva-Paterna et al, 2002 |
24 | Maximum GSI value | 11.46 [April-June] | 11.46 percent | Oliva-Paterna et al, 2002 |
25 | Oogenesis duration | From December to April | 6.0 months | Oliva-Paterna et al, 2002 |
26 | Resting period | A period of quiescence of 3 month [September-November] | 3.0 months | Oliva-Paterna et al, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | Beginning of 2 year [Both sex specified] | 2.0 years | Oliva-Paterna et al, 2002 |
27 | Age at sexual maturity | 1-2 [Most at 2 and 3, male specified] | 1.5 years | Soriguer et al, 2000 |
28 | Length at sexual maturity | 48-53 | 50.5 cm | Oliva-Paterna et al, 2002 |
30 | Male sexual dimorphism | Mature males exibit secondary sexual characters like the lamina circularis with a short manubrium, allowing external sex recognition | Absent | Perdices and Doadrio, 1977 |
30 | Male sexual dimorphism | A change of coloration is observed only during spawning activity: the male became pale [This spawning coloration. This spawning coloration disappeared within a few hours after spawning activity | Absent | Bohlen, 2000 |
31 | Onset of spermatogenesis | Early October | ['October'] | Oliva-Paterna et al, 2002 |
32 | Main spermatogenesis activity | Greatest increase in March | ['March'] | Oliva-Paterna et al, 2002 |
33 | Maximum GSI value | 1.52% [April-June] | 1.52 percent | Oliva-Paterna et al, 2002 |
34 | Spermatogenesis duration | From October to April | 7.0 months | Oliva-Paterna et al, 2002 |
35 | Resting period | Short quiescence period [August-September] | 3.0 months | Oliva-Paterna et al, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
39 | Spawning season | Late March to early July | ['March', 'July'] | Oliva-Paterna et al, 2002 |
39 | Spawning season | Starts in May throughout July | ['May', 'July'] | Perdices and Doadrio, 1977 |
40 | Spawning period duration | 12 [3.00 months, length of breeding season] | 12.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
44 | Spawning substrate | Dense vegetation | Phytophils | Bohlen, 2000 |
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 |
47 | Mating system | All males in the tank followed the female, the female penetrated into dense vegetation, spotted and one male embraced the female. The female started swimming and the circle began again, often with another male embracing the female | No category | Bohlen, 2000 |
48 | Spawning release | Multiple spawner or batch spawner: two batches per year per females | Multiple | Oliva-Paterna et al, 2002 |
48 | Spawning release | Multiple spawning have been suggested also for C. paludicola | Multiple | Marconato and Rasotto, 1989 |
49 | Parity | Iteroparous [Adult specimens have no more than two or three reproductive years] | Iteroparous | Perdices and Doadrio, 1977 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |