Trait completeness | 70% |
Total data | 121 |
References | 20 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 0.5-1.5 | 1.0 mm | Coad, 2005 |
1 | Oocyte diameter | 1-1.4 | 1.2 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.4 | 1.4 mm | Cassou and Le Louarn, 1991 |
1 | Oocyte diameter | 1-1.4 [Not specified] | 1.2 mm | Agence de l'eau, |
2 | Egg size after water-hardening | 1.3-1.4 [After swelling] | 1.35 mm | Pinder and Gozlan, 2004 |
2 | Egg size after water-hardening | 1.1-1.3 [After swelling] | 1.2 mm | Bonislawska and Winnicki, 2000 |
2 | Egg size after water-hardening | 1.25 ± 0.04, n=100 [Eggs stripped from mature females, fertilized and incubated in water: hydrated eggs] | 1.25 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | 1.14-1.31 [Egg swollen] | 1.23 mm | Bonislawska et al, 2000 |
2 | Egg size after water-hardening | Mean of 1.26 [Swollen egg] | 1.26 mm | Bonislawska et al, 1999 |
3 | Egg Buoyancy | Demersal | Demersal | Cassou and Le Louarn, 1991 |
4 | Egg adhesiveness | Sticky | Adhesive | Cassou and Le Louarn, 1991 |
4 | Egg adhesiveness | Adhesive | Adhesive | Gozlan et al, 2003 |
4 | Egg adhesiveness | Adhere to other eggs in the strip, highly adhesive chorion | Adhesive | Pinder and Gozlan, 2004 |
4 | Egg adhesiveness | Mucopolysaccharides contained in the ovarian fluid harden in water, adhering the eggs to the substraum | Adhesive | Bonislawska et al, 1999 |
5 | Incubation time | 10 | 10.0 days | Billard, 1997 |
5 | Incubation time | 5-6 [22-24°C], 6-7 [21°C] | 5.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 3-3.5 [At 24.7°C], also described as 6-7 days [At 21-22°C], and 4 [At 25-26°C] | 3.25 days | Pinder and Gozlan, 2004 |
5 | Incubation time | 5 days at 20°C; also described as 4 days in 20°C; also described as 5-6 days in 22-23.6°C | 5.5 days | Bonislawska et al, 1999 |
6 | Temperature for incubation | 22-24 | 23.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | From activation to hatching, water temperature ranged between 22.8 and 26.5°C | 22.8 °C | Pinder and Gozlan, 2004 |
6 | Temperature for incubation | Mean water temperature in the laboratory was 20°C (daily variations ±1°C) | 20.0 °C | Bonislawska et al, 1999 |
7 | Degree-days for incubation | 110-145 | 127.5 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 100-130 | 115.0 °C * day | Cassou and Le Louarn, 1991 |
7 | Degree-days for incubation | 75.5-80.7 | 78.1 °C * day | Pinder and Gozlan, 2004 |
7 | Degree-days for incubation | 99.2-101 | 100.1 °C * day | Bonislawska et al, 2000 |
7 | Degree-days for incubation | About 100 at 20°C | 100.0 °C * day | Bonislawska et al, 1999 |
7 | Degree-days for incubation | 110-145 | 127.5 °C * day | Agence de l'eau, |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 4-4.5 | 4.25 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | Mean 5.11, range 4.83-5.27 | 5.05 mm | Pinder and Gozlan, 2004 |
8 | Initial larval size | TL = 6.1, for eleuterembryo in developental stage A, just hatched (6 days 5 hours from the beginning of development) | 6.1 mm | Penaz, 1971 |
8 | Initial larval size | Slim larva, carrying a small yolk sac, was 4.25 mm long on the average (the smallest one 4.1 mm, the longest 4.4 mm) | 4.25 mm | Bonislawska et al, 1999 |
9 | Larvae behaviour | Pelagic, highly active near the surface | Pelagic | Bruslé and Quignard, 2001 |
9 | Larvae behaviour | Newly-emerged larvae swim actively | Demersal | Mann, 1996 |
9 | Larvae behaviour | The earliest embryos to hatch were onyl able to perform sudden bursts of activity and appeared to be able to swim a few centimetres from the bottom before sinking again. Those embryos that hatched lated, however, were able to perform more sustained swimming that were soon able to swim to the surface | Demersal | Pinder and Gozlan, 2004 |
9 | Larvae behaviour | A specific prolongation of embryonic development within the membane seems to be a fairly unusual development phenomenon; as a result the hatching larvae is capable of an independent life in water [Others described as: hatched larvae had no cement glands and were so advanced in develoment that were able to commence active life and form soals under the water surface as soon as they left the egg membranes while also described as that sun bleak larvae, as of other cyprinids, first attached themselves to the substraum, and sawm upward, to the surface, to fill the air bladder, only after having resorbed the yolk sac] | Demersal | Bonislawska et al, 1999 |
11 | Temperature during larval development | After hatching free-embryos and larvae in the aquarium were subsjected to temperatures ranging between 15.1 and 27.5°C, with mean daily temperatures ranging between 16.9 and 26°C (mean 21.6°C). | 15.1 °C | Pinder and Gozlan, 2004 |
11 | Temperature during larval development | Reared at 20°C | 20.0 °C | Bonislawska et al, 1999 |
12 | Sibling intracohort cannibalism | With the onset of spawning period, adults may turn on feeding on their own eggs and larvae | Absent | Pipoyan, 1996 |
12 | Sibling intracohort cannibalism | Throughout the spawing season, filial and hetero-cannibaslim was observed in all groups of individuals except parasitic males. Cannibalism in males guarding the nest site containing eggs was rare | Present | Gozlan et al, 2003 |
13 | Full yolk-sac resorption | 90-100 DD: By day 8, only a small portion of yolk reserves remained to be absorbed (less than 75.5-80.7 hours for incubation) at 21.6°C | 95.0 °C * day | Pinder and Gozlan, 2004 |
13 | Full yolk-sac resorption | Contents of small yolk sac were very quickly resorbed: 1-2 days at 20°C | 1.5 °C * day | Bonislawska et al, 1999 |
14 | Onset of exogeneous feeding | Onset of exogeneous feeding for the first embryo 88 hours at 21.6°C] .i.e. 3-16 hours after hatching | 9.5 °C * day | Pinder and Gozlan, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1 [Female] | 1.0 year | Le Louarn, 2001 |
15 | Age at sexual maturity | Sexual maturity is attained at the age of two years (both males and females) | 2.0 year | Bonislawska et al, 1999 |
16 | Length at sexual maturity | 5.4 | 5.4 cm | Gozlan et al, 2003 |
18 | Female sexual dimorphism | Females have a unique fold of skin in the shape of two, large rounded papilla around the genital opening | Present | Coad, 2005 |
18 | Female sexual dimorphism | Females have three small bulges near anus | Absent | Bonislawska et al, 1999 |
19 | Relative fecundity | Relative fecundity is very high from 300 thousand to 900 thousand egg per Kg | 300.0 thousand eggs/kg | Bonislawska et al, 1999 |
20 | Absolute fecundity | 0.4-3.5 | 1.95 thousand eggs | Coad, 2005 |
20 | Absolute fecundity | 0.6-2.3 | 1.45 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | Low ranging from 700 to 2100 eggs | 700.0 thousand eggs | Bonislawska et al, 1999 |
20 | Absolute fecundity | 100-200 (600) eggs per female | 150.0 thousand eggs | Agence de l'eau, |
21 | Oocyte development | Asynchronous | Asynchronous | Bruslé and Quignard, 2001 |
21 | Oocyte development | Three kind of ovocytes during the spanwing season | No category | Cassou and Le Louarn, 1991 |
24 | Maximum GSI value | Mean about 13%, up to 16% [In May] | 13.0 percent | Cassou and Le Louarn, 1991 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1 [Male] | 1.0 years | Le Louarn, 2001 |
27 | Age at sexual maturity | Sexual maturity is attained at the age of two years (both males and females) | 2.0 years | Bonislawska et al, 1999 |
27 | Age at sexual maturity | 1 [Sex not specified] | 1.0 years | Agence de l'eau, |
28 | Length at sexual maturity | 4.5-5.5 [Territorial male] | 5.0 cm | Gozlan et al, 2003 |
30 | Male sexual dimorphism | Prominent nuptial tubercles on the dorsal head surface, snout, on the lower jaw in three pairs on the upper jaw in two pairs for a total of about 60 tubercules. The genital opening is depressed | Present | Coad, 2005 |
30 | Male sexual dimorphism | Nuptial tubercles on male at maturity | Present | Billard, 1997 |
30 | Male sexual dimorphism | Reproducing males have white spawing tubercles characteristic of many male cyprinids in spawning condition | Absent | Bonislawska et al, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | No migration | No data | Agence de l'eau, |
39 | Spawning season | April-May | ['April', 'May'] | Billard, 1997 |
39 | Spawning season | April-May and July-August | ['April', 'May', 'July', 'August'] | Bruslé and Quignard, 2001 |
39 | Spawning season | March to September | ['March', 'April', 'May', 'June', 'July', 'August', 'September'] | Coad, 2005 |
39 | Spawning season | Mid-May to Mid-July | ['May', 'June', 'July'] | Le Louarn, 2001 |
39 | Spawning season | June to August | ['June', 'July', 'August'] | Cassou and Le Louarn, 1991 |
39 | Spawning season | Commences in May, depedning on thermal conditions, and last until August | ['May', 'August'] | Bonislawska et al, 1999 |
39 | Spawning season | May to July | ['May', 'June', 'July'] | Agence de l'eau, |
40 | Spawning period duration | 4-5 | 4.5 weeks | Bruslé and Quignard, 2001 |
40 | Spawning period duration | Few weeks | No data | Coad, 2005 |
40 | Spawning period duration | 8 [From May, 17 to July, 16] | 8.0 weeks | Cassou and Le Louarn, 1991 |
40 | Spawning period duration | Commences in May, depedning on thermal conditions, and last until August | No data | Bonislawska et al, 1999 |
41 | Spawning temperature | 18 is the miminum temperature required for reproduction | 18.0 °C | Coad, 2005 |
41 | Spawning temperature | 15-24 | 19.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 15-20 | 17.5 °C | Cassou and Le Louarn, 1991 |
41 | Spawning temperature | 16.0-20.4 | 18.2 °C | Gozlan et al, 2003 |
41 | Spawning temperature | Commnenced spawning at water temperature fo 15°C | 15.0 °C | Bonislawska et al, 1999 |
42 | Spawning water type | Sunbleak typically lay their eggs on marginal macrophytes that generally grouw out of anoxic silt | No category | Pinder and Gozlan, 2004 |
44 | Spawning substrate | Phytophil: in plants | Phytophils | Billard, 1997 |
44 | Spawning substrate | Around aquatic plants | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Around plants or on any flat surface | Phytophils | Coad, 2005 |
44 | Spawning substrate | Large leafs, around stems, and floatings objects | No category | Cassou and Le Louarn, 1991 |
44 | Spawning substrate | Phytophils: eggs are laid in thin ribbons on plat leaves and stems | Phytophils | Mann, 1996 |
44 | Spawning substrate | Phytophil | Phytophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Phytophil | Phytophils | Balon, 1975 |
44 | Spawning substrate | Submerged plants, roots and sunken objects | Phytophils | Bonislawska et al, 1999 |
44 | Spawning substrate | On plants | Phytophils | Agence de l'eau, |
45 | Spawning site preparation | Rudimentary nest | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Females may also lay their eggs in a disc-shaped patch on any flat surface | Susbtrate chooser | Coad, 2005 |
45 | Spawning site preparation | Kind of a nest | No category | Cassou and Le Louarn, 1991 |
45 | Spawning site preparation | Male guards a single nest site, once a nest site is obtained, the male either encircled or remained a fixed position at the nest site, at times cleaning the nest surface with his mouth | No category | Gozlan et al, 2003 |
45 | Spawning site preparation | Substratum choosers | No category | Balon, 1975 |
45 | Spawning site preparation | Spawn on any smooth objects such as branches, floating leaves, plastic debris, even bottom of boats. | No category | Gozlan et al, 2003b |
45 | Spawning site preparation | Females deposits their eggs in a ribbon | No category | Bonislawska et al, 1999 |
47 | Mating system | An individual male guard a nest, and females visit the nest | No category | Gozlan et al, 2003 |
48 | Spawning release | Several spawnings occur over a few weeks | Multiple | Coad, 2005 |
48 | Spawning release | Multiple spawner | Multiple | Rinchard, 1996 |
48 | Spawning release | Fractional asynchronous | Fractional | Cassou and Le Louarn, 1991 |
48 | Spawning release | Laid in strings. 50-350 eggs | No category | Coad, 2005 |
48 | Spawning release | Fractionnal spawner : 3 spawns or five generations of ovocytes released by batch of 20-30 | Multiple | Bruslé and Quignard, 2001 |
48 | Spawning release | Spawing is asynhcronous and fractional: the spawning consists of ribbon of 8-10 cm | Fractional | Le Louarn, 2001 |
48 | Spawning release | Female lay one or several ribbons of eggs | Multiple | Cassou and Le Louarn, 1991 |
48 | Spawning release | Female release a strip of up to 80 eggs | No category | Gozlan et al, 2003 |
48 | Spawning release | Batch spawner | Multiple | Gozlan et al, 2003b |
48 | Spawning release | Typical multiple spawners | Multiple | Fredrich et al, 2003 |
48 | Spawning release | Egg are laid in batches, so spawners spawn every few or every several days. Also observed that each female laid 3-5 batches of eggs | Multiple | Bonislawska et al, 1999 |
48 | Spawning release | Fractional spawning with 3 to 5 generations of oocytes | Fractional | Agence de l'eau, |
48 | Spawning release | Batch spawning cyprinid | Multiple | Pinder et al, 2005 |
49 | Parity | Life span is about 4-6 years with growth fairly continuous over this period | No category | Coad, 2005 |
49 | Parity | Live up to 2-3 (5) years | No category | Agence de l'eau, |
50 | Parental care | Eggs are guarded and fanned by the male who covers them with a bacteriostatic thermal mucus | Biparental care | Coad, 2005 |
50 | Parental care | Eggs are guarded by the male | Male parental care | Bruslé and Quignard, 2001 |
50 | Parental care | Eggs are guarded by the male during the time of incubation (about 10 days) | Male parental care | Billard, 1997 |
50 | Parental care | Eggs are protected | No category | Le Louarn, 2001 |
50 | Parental care | Male guard and ventilate the "nest" until hatching | Male parental care | Cassou and Le Louarn, 1991 |
50 | Parental care | Male guards a nest, chases and attcaks any untruders (bittig and head-butting) | Male parental care | Gozlan et al, 2003 |
50 | Parental care | The egg guarding behaviour of the males | No category | Gozlan et al, 2003b |
50 | Parental care | Sun bleak are egg guarder; as soon as he eggs are fertilized, the male starts to fan and guard them eagerly | No category | Bonislawska et al, 1999 |
50 | Parental care | Male aerate the eggs | Male parental care | Agence de l'eau, |