Trait completeness | 64% |
Total data | 83 |
References | 16 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 2.4-3.1 [Not specified] | 2.75 mm | Smith et al, 2004 |
1 | Oocyte diameter | 2.6 [Larger diameter, the other is 1.7] | 2.6 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.0-1.5 to 2.5-3.0 | 1.25 mm | Oliver and Carrel, 2001 |
2 | Egg size after water-hardening | 2.59 ± 0.04 x 1.74 ± 0.07 [n = 63] | 2.59 mm | Aldridge, 1999 |
2 | Egg size after water-hardening | 1.3-2.6 [Seems to be fertilized eggs] | 1.95 mm | Bonislawska et al, 2001 |
3 | Egg Buoyancy | Dense, sinking quickly in freshwater | Demersal | Smith et al, 2004 |
3 | Egg Buoyancy | Demersal | Demersal | Bruslé and Quignard, 2001 |
5 | Incubation time | 1.5 | 1.5 days | Smith et al, 2004 |
5 | Incubation time | 14-21 [To leave the mussel ?] | 17.5 days | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | 20 | 20.0 °C | Aldridge, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 3.3 | 3.3 mm | Smith et al, 2004 |
8 | Initial larval size | 3.3 [Pigmented eye only at 7.9] | 3.3 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 3.3 | 3.3 mm | Aldridge, 1999 |
9 | Larvae behaviour | Remain in the mussel | Demersal | Bruslé and Quignard, 2001 |
9 | Larvae behaviour | Positively rheotaxic, remains in the mussel | Demersal | Smith et al, 2004 |
10 | Reaction to light | Negatively phototaxic | Photophobic | Smith et al, 2004 |
10 | Reaction to light | Photophobic | Photophobic | Bruslé and Quignard, 2001 |
11 | Temperature during larval development | 20 | 20.0 °C | Aldridge, 1999 |
13 | Full yolk-sac resorption | Mussels incubate the eggs for 2-4 weeks, until the yolk is absorbed when the young bitterling swim out the exhalant siphon of the living mussel] | 3.0 °C * day | Mills and Reynolds, 2002 |
14 | Onset of exogeneous feeding | 560 [28 days at 20°C] | 560.0 °C * day | Aldridge, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1 [Both sex] | 1.0 year | Smith et al, 2004 |
15 | Age at sexual maturity | 1 | 1.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 1 [Sex not precised] | 1.0 year | Oliver and Carrel, 2001 |
15 | Age at sexual maturity | 2-3 [Unsexed] | 2.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 1 [Both sex] | 1.0 year | Rosecchi et al, 2001 |
15 | Age at sexual maturity | 1 [Both sex for amarus] | 1.0 year | Bensettiti and Gaudillat, 2002 |
16 | Length at sexual maturity | 3-3.5 | 3.25 cm | Smith et al, 2004 |
16 | Length at sexual maturity | 3-3.5 | 3.25 cm | Bruslé and Quignard, 2001 |
18 | Female sexual dimorphism | Long ovipositors that they use to place their eggs onto the gills of a mussel trough the mussel'sexhalant siphon | Absent | Smith et al, 2004 |
18 | Female sexual dimorphism | Female develops a conduit ovipository by which it deposits its ovules between the gills of the bivalve | Absent | Fishbase, 2006 |
18 | Female sexual dimorphism | Females use their long ovipositors to force eggs throught the exhalant siphon into the gills of the museel host | Absent | Mills and Reynolds, 2002 |
20 | Absolute fecundity | 0.08-0.250 are the typical breeding season fecundity | 0.17 thousand eggs | Smith et al, 2004 |
20 | Absolute fecundity | 0.095-0.480 | 0.29 thousand eggs | Bruslé and Quignard, 2001 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
24 | Maximum GSI value | 7-10 | 8.5 percent | Bruslé and Quignard, 2001 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1 [Both sex] | 1.0 years | Smith et al, 2004 |
27 | Age at sexual maturity | 1 [Sex not precised] | 1.0 years | Oliver and Carrel, 2001 |
27 | Age at sexual maturity | 2-3 [Unsexed] | 2.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 1 [Both sex] | 1.0 years | Rosecchi et al, 2001 |
27 | Age at sexual maturity | 1 [Both sex for amarus] | 1.0 years | Bensettiti and Gaudillat, 2002 |
28 | Length at sexual maturity | 3-3.5 [Both sex] | 3.25 cm | Smith et al, 2004 |
30 | Male sexual dimorphism | Develop bright nuptial coloration | Present | Smith et al, 2004 |
30 | Male sexual dimorphism | Breeding tubercles only in males, only on the head | Absent | Witkowski and Rogowska, 1991 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | No migration | No data | Agence de l'eau, |
39 | Spawning season | April-August with a peak in May | ['April', 'May', 'June', 'July', 'August'] | Smith et al, 2004 |
39 | Spawning season | April-June | ['April', 'June'] | Billard, 1997 |
39 | Spawning season | April-June | ['April', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | Early spring | ['April', 'May', 'June'] | Aldridge, 1999 |
39 | Spawning season | April to August | ['April', 'May', 'June', 'July', 'August'] | Oliver and Carrel, 2001 |
39 | Spawning season | April to June | ['April', 'May', 'June'] | Fishbase, 2006 |
39 | Spawning season | April to mid-June | ['April', 'May', 'June'] | Terver, 1984 |
39 | Spawning season | April to August for amrus | ['April', 'May', 'June', 'July', 'August'] | Bensettiti and Gaudillat, 2002 |
40 | Spawning period duration | 9-10 | 9.5 weeks | Terver, 1984 |
41 | Spawning temperature | 15-21 | 18.0 °C | Oliver and Carrel, 2001 |
41 | Spawning temperature | 22 [Rerared conditions] | 22.0 °C | Mills and Reynolds, 2002 |
41 | Spawning temperature | 15-21 for amarus | 18.0 °C | Bensettiti and Gaudillat, 2002 |
42 | Spawning water type | In tributary of the river, near to banks | No category | Mills and Reynolds, 2002 |
44 | Spawning substrate | Mussels | Ostracophils | Smith et al, 2004 |
44 | Spawning substrate | Spawns on the gills of living unionid freshwater mussels | Ostracophils | Smith et al, 2001 |
44 | Spawning substrate | Mussels | Ostracophils | Billard, 1997 |
44 | Spawning substrate | Mussels [Unionidae] | Ostracophils | Oliver and Carrel, 2001 |
44 | Spawning substrate | Ostracophils | Ostracophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Ostracophils | Ostracophils | Balon, 1975 |
44 | Spawning substrate | Obligate spawning relationship between a species of freshwater fish, the bitterling, and four species of freshwater mussels [The mussels were collected along the silt bottoms near to the banks] | Ostracophils | Mills and Reynolds, 2002 |
45 | Spawning site preparation | Males defend territories around one or several mussel | No category | Smith et al, 2004 |
45 | Spawning site preparation | Male defend a territory around one or several mussels, then a he brings a female | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Male defend territories around mussels to which they lead females to spawn | No category | Smith et al, 2001 |
45 | Spawning site preparation | Males defend territories around freswater mussels | No category | Aldridge, 1999 |
45 | Spawning site preparation | Males defend territories around freswater mussels | No category | Oliver and Carrel, 2001 |
45 | Spawning site preparation | Maes defend a territory around a mussel, for amarus | No category | Bensettiti and Gaudillat, 2002 |
47 | Mating system | One male and one female each time | Monogamy | Bruslé and Quignard, 2001 |
48 | Spawning release | Batch spawners with determinate fecundity; breeding season is fixed at the onset of the spawning season. with egg number in the ovary declining over the spawning season | Multiple | Smith et al, 2004 |
48 | Spawning release | Several batches of eggs, the time between two batch is about 5-20 mn | Multiple | Bruslé and Quignard, 2001 |
48 | Spawning release | Female can spawn in more than one mussel and lay 50-100 clutches of 1-6 eggs during a breeding season | No category | Smith et al, 2001 |
48 | Spawning release | Multiple spawner: up to 5 | Multiple | Oliver and Carrel, 2001 |
48 | Spawning release | Bouts of spawning last 1-3 days, with the interval between bouts usually 5-7 days. once a batch of eggs has ovulated. females are capable of spawning up to at least five occasions on the same day | Multiple | Smith et al, 2004 |
48 | Spawning release | up to five batches of 40-100 eggs | Multiple | Oliver and Carrel, 2001 |
48 | Spawning release | Multiple spawner: up to 5, batch of 40-100 eggs | Multiple | Bensettiti and Gaudillat, 2002 |
49 | Parity | 2-3 up to 5 | No category | Bruslé and Quignard, 2001 |
50 | Parental care | Males defend territories around one or several mussel | No category | Smith et al, 2004 |
50 | Parental care | Male defend a territory around one or several mussels, then a he brings a female | Male parental care | Bruslé and Quignard, 2001 |
50 | Parental care | Male guards the eggs and larvae until they quit the mussel | Male parental care | Billard, 1997 |
50 | Parental care | Non guarders, brood hiders [The male keeps the eggs and alevins until they leave the refuge] | No care | Fishbase, 2006 |