Trait completeness | 86% |
Total data | 189 |
References | 38 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.2-1.5 | 1.35 mm | Mellinger, 2002 |
1 | Oocyte diameter | 1.0-1.7 | 1.35 mm | Internet, 2005 |
1 | Oocyte diameter | 1.5-1.7 | 1.6 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.5-1.7 | 1.6 mm | Persat, 2001 |
1 | Oocyte diameter | 1.2-1.5 | 1.35 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 1.4 [Mean diameter of mature, fully yolked, ovarian oocyte] | 1.4 mm | Olden et al, 2006 |
2 | Egg size after water-hardening | 1.29 ± 0.05, n=57 [Eggs stripped from mature females, fertilized and incubated in water: hydrated eggs] | 1.29 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | 1.25-1.46 | 1.35 mm | Battle, 1940 |
3 | Egg Buoyancy | Demersal | Demersal | Internet, 2005 |
4 | Egg adhesiveness | Highly adhesive | Adhesive | Spillmann, 1961 |
4 | Egg adhesiveness | Released eggs stick to the leaves of plants within a few seconds irrespective of whether fertilisation has been successful | Adhesive | Horvath et al, 1992 |
4 | Egg adhesiveness | Adhesive | Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Adhesive | Adhesive | Scott and Crossman, 1973 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | Adhesive | Adhesive | Scholfield, 2005 |
4 | Egg adhesiveness | When first laid the whole surface is adhesive, but the quality is lost as they have become water hardened a,d attached to aquatic plants [The eggs are of a mucilaginous character and adhere readily to aquatic plants to which they usually attached singly, rarely in twos or threes and at intervals of one-half to one inch] | Adhesive | Battle, 1940 |
4 | Egg adhesiveness | Adhesive | Adhesive | Kestemont and Mélard, 1994 |
4 | Egg adhesiveness | Release eggs adhere to the vegetation | Adhesive | Kobayashi et al, 2002 |
4 | Egg adhesiveness | Spawn of goldfish is yellow-green and sticks to the substrate | Adhesive | Sczerbowski and Szczerbowski, 1996 |
4 | Egg adhesiveness | Eggs adhere to substrate, usually vegetation at spawning site | Adhesive | Goodyear et al, 1982 |
4 | Egg adhesiveness | The goldfish eggs adhered to the Petri dish and were not dislodged by this procedure | Adhesive | Wiegand et al, 1988 |
5 | Incubation time | About 7 | 7.0 days | Spillmann, 1961 |
5 | Incubation time | Few days | No data | Horvath et al, 1992 |
5 | Incubation time | 5 [20°C], 3-4 [20-27.5°C] | 3.5 days | Internet, 2005 |
5 | Incubation time | 8 [20°C] | 8.0 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 3-4 [15.5-29.5], 64-72 hours [24-28°C], 76 hours at [25°C] | 3.5 days | Scott and Crossman, 1973 |
5 | Incubation time | 3-7 days | 5.0 days | Scholfield, 2005 |
5 | Incubation time | [46 to 54 hours at 84°F; 4-14 days; 5-7 days at 70-75°F, 3-4 days at 18.5-29.5°C] | 9.0 days | Battle, 1940 |
5 | Incubation time | 6.0 [Mean time to egg hatch within the range of average post-spawning the range post-spawning water temperatures] | 6.0 days | Olden et al, 2006 |
5 | Incubation time | The mean time to 50% hatch at 27°C was 2.0 days in all four experiments, involving that temperature. At 22°C, the mean time to 50% hatch was 3.8 ±0.4 days and at 17°C it was 7.1 ± 0.4 days. At 12°C, the mean time to 50% hatch was more variable at 14.1 ±2.5 days. | 3.8 days | Wiegand et al, 1988 |
5 | Incubation time | Hatching occurs after 5-8 days | 6.5 days | Szczerbowski and Szczerbowski, 1996 |
5 | Incubation time | About 1 week | 1.0 days | Kestemont and Mélard, 1994 |
5 | Incubation time | Eggs hatch in 2-1/2 to 7 days at 82-60°F | 1.5 days | Goodyear et al, 1982 |
6 | Temperature for incubation | 20-27.5 | 23.75 °C | Internet, 2005 |
6 | Temperature for incubation | 20°C | 20.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | 24-28 [But could be incubated at 15.5-29.5] | 26.0 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 25 [18.5-29.5°C] | 24.0 °C | Battle, 1940 |
6 | Temperature for incubation | The optimum temperature for rearing eggs and larvae was 22°C [At 27°C and 17°C, there was a higher indidence of abnormal larvae at hatching and reduced viability compared to 22°C in some, but not all, experiments. Eggs incubated at 12°C produced inviable larvae. High proportions of 12°C larvae were abnormal at hatching and fish raised at 12°C failed to feed] | 22.0 °C | Wiegand et al, 1988 |
6 | Temperature for incubation | Compared with incubation at a constant 22°C, exposure of goldfish embryos and larvae to 13°C, under a variety of thermal protocols, caused increased frequencis of abnormal development and, in some cases, reduced survival to hatching. | 22.0 °C | Wiegand et al, 1989 |
6 | Temperature for incubation | Similarly, goldfish (Carassius auratus) eggs incubated at 12°C yielded significantly higher frequencies of abnormal larvae than those incubated at highest temperatures | 12.0 °C | Kucharczyk et al, 1997 |
7 | Degree-days for incubation | 80-100 | 90.0 °C * day | Internet, 2005 |
7 | Degree-days for incubation | 100-160 | 130.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 75 [3 days at 25°C] | 75.0 °C * day | Persat, 2001 |
7 | Degree-days for incubation | About 70-90 | 80.0 °C * day | Scott and Crossman, 1973 |
7 | Degree-days for incubation | About 90 | 90.0 °C * day | Kestemont and Mélard, 1994 |
2 | Egg size after water-hardening | 1.60 | 1.6 mm | Becker, 1983 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | Mostly 4-4.5 [rarely 3.0 or 5.0] | 4.25 mm | Internet, 2005 |
8 | Initial larval size | 4 | 4.0 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 4.5 | 4.5 mm | Battle, 1940 |
8 | Initial larval size | 3.5 | 3.5 mm | Olden et al, 2006 |
8 | Initial larval size | Newly hatched larvae are 5.8 mm long | 5.8 mm | Szczerbowski and Szczerbowski, 1996 |
8 | Initial larval size | Mean initial length at 2 dph 6.3 +/- 0.7 | 6.3 mm | Coutinho et al, 2006 |
9 | Larvae behaviour | Benthic, remain near the spawning area, then near the surface after yolk sac is absorbed | Demersal | Internet, 2005 |
9 | Larvae behaviour | At hatching, the larva is restricted in the movement by the weight of the yolk sac. The larva shows a positive thigmotropism, adhering to the aquarium walls or any fragments of plants. | Demersal | Battle, 1940 |
9 | Larvae behaviour | During 3 days after hatching yolk-feeding larva is fixed to submerged plants | Demersal | Szczerbowski and Szczerbowski, 1996 |
10 | Reaction to light | Larvae are not photophobic | Photopositive | Mann, 1996 |
11 | Temperature during larval development | Could tolerate 30 or more | 30.0 °C | Spillmann, 1961 |
11 | Temperature during larval development | Compared with incubation at a constant 22°C, exposure of goldfish embryos and larvae to 13°C, under a variety of thermal protocols, caused increased frequencies of abnormal development and, in some cases, reduced survival to hatching. | 22.0 °C | Wiegand et al, 1989 |
11 | Temperature during larval development | Reared at 21°C | 21.0 °C | Pozernik and Wiegand, 1997 |
11 | Temperature during larval development | The optimum temperature for rearing eggs and larvae was 22°C [At 27°C and 17°C, there was a higher indidence of abnormal larvae at hatching and reduced viability compared to 22°C in some, but not all, experiments. Eggs incubated at 12°C produced inviable larvae. High proportions of 12°C larvae were abnormal at hatching and fish raised at 12°C failed to feed] | 22.0 °C | Wiegand et al, 1988 |
11 | Temperature during larval development | Reared at 24°C | 24.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | Reared at 25°C | 25.0 °C | Battle, 1940 |
11 | Temperature during larval development | A central heater-thermostat unit was set to maintain a temperature àf 24°C | 24.0 °C | Kaiser et al, 2003 |
11 | Temperature during larval development | The experiments investigated the effects of temperature (20, 24 and 28°C) […] Although goldfish is considered as a thermophilic species, survival was lower at 28°C than at 20 and 24°C in Experiment 1, probably due to a decrease of water quality (caused by high feeding level, up to 90% in expeirment 1) and faster development of pathogens in the rearing tanks | 20.0 °C | Kestemont, 1995 |
12 | Sibling intracohort cannibalism | Cannibaslim by the parents on eggs and larvae ! | Absent | Horvath et al, 1992 |
13 | Full yolk-sac resorption | By one and one-half to two and one-half days,a length of 5.8 millimeters is attained, and the yolk sac has been reduced to a narrow tubular band. At seven to eight days (6.8 millimeter stage), the yolk material has practically all disappeared.At 25°C | 5.8 °C * day | Battle, 1940 |
13 | Full yolk-sac resorption | Yolk was absorbed to be absent or present as a thin ribbon only by day 2 at 27°C, day 4 at 22°C, and day 6 at 17°C | 2.0 °C * day | Wiegand et al, 1988 |
14 | Onset of exogeneous feeding | At the day 8th and 10th after hatching larva is 7 mm long. At that time active feeding begins | 8.0 °C * day | Szczerbowski and Szczerbowski, 1996 |
14 | Onset of exogeneous feeding | Each experimental tank was stocked with 83 3-4-day-old goldfish of the cornet variety at a density of 6.5 fish. L-1, and all trials started at the time of first exogenous feeding (at 25°C) | 3.5 °C * day | Kaiser et al, 2003 |
14 | Onset of exogeneous feeding | Three days after hatching at 20°C, the young larvae swim towards the surface for fulfill their swimbladder, and then start to search food | 20.0 °C * day | Kestemont and Mélard, 1994 |
8 | Initial larval size | 3-5 | 4.0 mm | Becker, 1983 |
9 | Larvae behaviour | benthic | Demersal | Becker, 1983 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2 [In France, only if water display a temperature of 20 or more] | 2.0 year | Spillmann, 1961 |
15 | Age at sexual maturity | 2-3 | 2.5 year | Internet, 2005 |
15 | Age at sexual maturity | 1-2 [sex not specified] | 1.5 year | Scholfield, 2005 |
15 | Age at sexual maturity | 3.5 [Both sex] | 3.5 year | Olden et al, 2006 |
15 | Age at sexual maturity | Usually at 2 in our latitudes, sex not specified | 2.0 year | Kestemont and Mélard, 1994 |
15 | Age at sexual maturity | In their natural area of distribution goldfish mature at the age of 1-2 years | 1.5 year | Sczerbowski and Szczerbowski, 1996 |
16 | Length at sexual maturity | 13.5 [Both sex] | 13.5 cm | Olden et al, 2006 |
19 | Relative fecundity | 160-200 | 180.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | Around 100 | 100.0 thousand eggs/kg | Kestemont and Mélard, 1994 |
20 | Absolute fecundity | Mean 14 [2 to 400] | 14.0 thousand eggs | Internet, 2005 |
20 | Absolute fecundity | 10-80 | 45.0 thousand eggs | Persat, 2001 |
20 | Absolute fecundity | 5.3 [Total number of eggs or offsprings per breeding season] | 5.3 thousand eggs | Olden et al, 2006 |
20 | Absolute fecundity | 48-60 [in April] and 38-54 [In June] | 54.0 thousand eggs | Wisniewolski, 1988 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
21 | Oocyte development | Asynchronous | Asynchronous | Kagawa et al, 1983 |
21 | Oocyte development | Asynchronous | Asynchronous | Papadopol and Weinberger, 1975 |
21 | Oocyte development | Exhibit group synchronous oocyte development | No category | Kobayashi et al, 2002 |
22 | Onset of oogenesis | December [GSI increased slowly from December to February, from 3.9 ±0.7 to 5.2 ± 1.0) | ['January', 'February', 'December'] | Kagawa et al, 1983 |
22 | Onset of oogenesis | GSI gradually increased from August to February (From 2.0 ±0.2 to 3.7 ±0.5) | ['January', 'February', 'August', 'September', 'October', 'November'] | Kobayashi et al, 1986 |
22 | Onset of oogenesis | Females commence vitellogenesis during winter | ['January', 'February', 'March'] | Kobayashi et al, 2002 |
23 | Intensifying oogenesis activity | March until April [GSI rapidly increased in March, and after the first ovulation second important increase in April] | ['March', 'April'] | Kagawa et al, 1983 |
23 | Intensifying oogenesis activity | GSI rapidly increased in April (6.4 ± 1.0) | ['April'] | Kobayashi et al, 1986 |
24 | Maximum GSI value | 18.7 ± 0.8 (April 30) | 18.7 percent | Kagawa et al, 1983 |
24 | Maximum GSI value | 10.5 ± 1.2 (May) | 10.5 percent | Kobayashi et al, 1986 |
24 | Maximum GSI value | 30 | 30.0 percent | Bruslé and Quignard, 2001 |
25 | Oogenesis duration | Goldfish mature in the spring | 4.0 months | Aida, 1988 |
26 | Resting period | August | 2.0 months | Kobayashi et al, 1986 |
26 | Resting period | 1.0 ± [August] | 1.0 months | Kobayashi et al, 1986 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2 | 2.0 years | Spillmann, 1961 |
27 | Age at sexual maturity | 2 | 2.0 years | Internet, 2005 |
27 | Age at sexual maturity | 1-2 [sex not specified] | 1.5 years | Scholfield, 2005 |
27 | Age at sexual maturity | 3.5 [Both sex] | 3.5 years | Olden et al, 2006 |
28 | Length at sexual maturity | 13.5 [Both sex] | 13.5 cm | Olden et al, 2006 |
30 | Male sexual dimorphism | Tiny white bumps on the head and around the pectoral fin | Absent | Horvath et al, 1992 |
30 | Male sexual dimorphism | Male bears nuptial tubercles on head, opercules, and first rays of pectoral fins | Present | Billard, 1997 |
30 | Male sexual dimorphism | Nuptial tubercles fune, on opercles, sometimes on back, and a few on pectotal fins of breeding males | Present | Scott and Crossman, 1973 |
30 | Male sexual dimorphism | During spawning fish are more brightly coloured than usually. During spawning males have hish locomotor activity; they are covered with breeding tubercles especially on the head and abdomen near pectoral fins, and their general coloration changes to purple | Present | Sczerbowski and Szczerbowski, 1996 |
33 | Maximum GSI value | 3.2 ±0.4 [May] | 3.2 percent | Kobayashi et al, 1986 |
35 | Resting period | 0.3 ± 0.1 [August, but a large increased was oberseved in the Autum: about 4%)] | 2.0 months | Kobayashi et al, 1986 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | No migration | No data | Agence de l'eau, |
36 | Spawning migration distance | Move inshore short distances into littoral areas or tributaries beginning at about 45°F | 45.0 km | Goodyear et al, 1982 |
37 | Spawning migration period | In the spring, when water temperatue is about 10-14°C | ['April', 'May', 'June'] | Ciolac, 2004 |
37 | Spawning migration period | Move inshore short distances into littoral areas or tributaries beginning at about 45°F | No data | Goodyear et al, 1982 |
39 | Spawning season | April trough July | ['April', 'July'] | Internet, 2005 |
39 | Spawning season | First warm days of spring | ['April', 'May', 'June'] | Horvath et al, 1992 |
39 | Spawning season | May 1 until June 9 | ['May', 'June'] | Kobayashi et al, 1986 |
39 | Spawning season | Mid-March until End of June | ['March', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | March until June | ['March', 'April', 'May', 'June'] | Billard, 1997 |
39 | Spawning season | June-July | ['June', 'July'] | Billard, 1997 |
39 | Spawning season | June-July | ['June', 'July'] | Persat, 2001 |
39 | Spawning season | May-June | ['May', 'June'] | Scott and Crossman, 1973 |
39 | Spawning season | Spring and summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Scholfield, 2005 |
39 | Spawning season | Begins early in the spring and occurs at frequent intervals from April to August | ['April', 'May', 'June', 'July', 'August'] | Battle, 1940 |
39 | Spawning season | June-July | ['June', 'July'] | Kestemont and Mélard, 1994 |
39 | Spawning season | Spawning season of goldfish begins in spring and lasts up to the end of summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Sczerbowski and Szczerbowski, 1996 |
39 | Spawning season | Mid-April to Mid-August, usually May-June | ['April', 'May', 'June', 'July', 'August'] | Goodyear et al, 1982 |
40 | Spawning period duration | 4-5 | 4.5 weeks | Kobayashi et al, 1986 |
41 | Spawning temperature | 20-25 [In fish farm] | 22.5 °C | Spillmann, 1961 |
41 | Spawning temperature | Around 15°C [Garden ponds] | 15.0 °C | Horvath et al, 1992 |
41 | Spawning temperature | 15-23 [but also 18-29.5] | 19.0 °C | Internet, 2005 |
41 | Spawning temperature | 16-17 | 16.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 20-25 | 22.5 °C | Persat, 2001 |
41 | Spawning temperature | Above 16 | 16.0 °C | Scholfield, 2005 |
41 | Spawning temperature | 15 [Temperature at which spawning is typically initiated] | 15.0 °C | Olden et al, 2006 |
41 | Spawning temperature | >17 | 17.0 °C | Gillet and Quétin, 2006 |
41 | Spawning temperature | About 20°C | 20.0 °C | Kestemont and Mélard, 1994 |
41 | Spawning temperature | Beginning at about 55°F; spawning may continue throughout the summer if water temperature remains above 60°F | 55.0 °C | Goodyear et al, 1982 |
42 | Spawning water type | Creeks, ditches, ponds and reservoirs | Stagnant water | Internet, 2005 |
42 | Spawning water type | Seeks warm, weedy shallows | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Stagnant water or with a weak flow | Stagnant water | Belova, 1981 |
42 | Spawning water type | Current-free areas in lower reaches of rivers, bays, harbors, lagoons, marshes, and flooded lowlands | Flowing or turbulent water | Goodyear et al, 1982 |
43 | Spawning depth | Shallow waters | No data | Internet, 2005 |
43 | Spawning depth | Shallow | No data | Scott and Crossman, 1973 |
43 | Spawning depth | Just before spawning fish go to shallow places overgrown with aquatic plants | No data | Sczerbowski and Szczerbowski, 1996 |
43 | Spawning depth | 2-12 feet | 7.0 m | Goodyear et al, 1982 |
44 | Spawning substrate | Plants | Phytophils | Spillmann, 1961 |
44 | Spawning substrate | Dense vegetation | Phytophils | Horvath et al, 1992 |
44 | Spawning substrate | Aquatic vegetation, submerged tree branches, roots, leaves | Phytophils | Internet, 2005 |
44 | Spawning substrate | Aquatic plants | Phytophils | Persat, 2001 |
44 | Spawning substrate | Submerged aquatic plants or willow roots | Phytophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Phytophils: eggs adhere to submerged macrophytes | Phytophils | Mann, 1996 |
44 | Spawning substrate | Phytophil | Phytophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Phytophils | Phytophils | Balon, 1975 |
44 | Spawning substrate | Vegetation, roots or fixed objects | Phytophils | Scholfield, 2005 |
44 | Spawning substrate | Member of the phytophilous group | Phytophils | Belova, 1981 |
44 | Spawning substrate | Aquatic plant substrate | Phytophils | Kestemont and Mélard, 1994 |
44 | Spawning substrate | Release eggs adhere to the vegetation | Phytophils | Kobayashi et al, 2002 |
44 | Spawning substrate | Just before spawning fish go to shallow places overgrown with aquatic plants | Phytophils | Sczerbowski and Szczerbowski, 1996 |
44 | Spawning substrate | Eggs are scattered over thick vegetation and mud, sand, clay, or gravel; also deposited on undersides of boats and harbor pilings | Lithophils | Goodyear et al, 1982 |
45 | Spawning site preparation | No, deposit its eggs | No category | Scott and Crossman, 1973 |
45 | Spawning site preparation | Scatter their adhesive eggs | Open water/substratum scatter | Scholfield, 2005 |
45 | Spawning site preparation | Non-territorial | No category | Kobayashi et al, 2002 |
46 | Nycthemeral period of oviposition | Spawning most often occurs in bright sunny mornings | Day | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | The spawing and laying of eggs usually commences at dawn | Dawn | Horvath et al, 1992 |
46 | Nycthemeral period of oviposition | Over a period from 7 a.m. to 10 a.m. [Spawning usually starts at daybreak and lasts till mid-afternoon] | Day | Battle, 1940 |
46 | Nycthemeral period of oviposition | Ovulation occurs near dawn | Dawn | Kobayashi et al, 2002 |
47 | Mating system | Each female may be pursued by several males | No category | Internet, 2005 |
47 | Mating system | Each mature female ready to release eggs is followed by a group of males […], the relase of larbe numbers of eggs and milt occurs. | Promiscuity | Horvath et al, 1992 |
47 | Mating system | The female may be accompanied by two or more males | No category | Scott and Crossman, 1973 |
47 | Mating system | Small,desorganized groups of males actively follow females, frequently initiating physical contact (nudging) and inspecting their urogenital and gill regions where pheromones are released. Following behavior typically leads to active chasing, the intensity of which increases until the time of ovulation as males appear to compete to be closest to the female (s), at times pushing each other. Once ovulated, females become sexually receptive and initiate spawning acts by entering aquatic vegetation. typically,one/few male (s) will enter vegetation witha receptive femaleand then swim rapidly with the female through a small arc, at which time the female release (oviposi) eggs and the male (s) will release (ejaculate) sperm to complete a spawning act. Female spanwing behaviour will continue until all ovulated eggs are released, and may involve a hundred or more oviposition acts over several hours with various males | Promiscuity | Kobayashi et al, 2002 |
47 | Mating system | Several males follow one female. In the spawning ground they form a tight group. Females release spawn, which is immediatly fertilized. Spawninf act may be repeated with different frequency which depends on temperature. Time intervals between batches are inversely related to spawners' body length | Promiscuity | Sczerbowski and Szczerbowski, 1996 |
48 | Spawning release | 3-4 spawnings in reared conditions | No category | Spillmann, 1961 |
48 | Spawning release | Spawn several times under natural conditions | Multiple | Aida, 1988 |
48 | Spawning release | Female are able to spawn more than once each spawning season | Multiple | Internet, 2005 |
48 | Spawning release | Multiple spawner: up to 4 a year | Multiple | Persat, 2001 |
48 | Spawning release | In favourable conditions fish may spawn several times in a season | Multiple | Horvath et al, 1992 |
48 | Spawning release | Deposited on substrates in single from; can be very dense in certain areas because of repeated deposition | Total | Internet, 2005 |
48 | Spawning release | In rearing conditions, up to 3-4 spawnings per season | No category | Billard, 1997 |
48 | Spawning release | Batch spawner | Multiple | Scholfield, 2005 |
48 | Spawning release | In the region where temperatures of water maintains above an higher value during several months, several spawning could be observed in the same breeders | Multiple | Kestemont and Mélard, 1994 |
48 | Spawning release | Ovulate oneto several times over a protracted spring-summer spanwing season | Multiple | Kobayashi et al, 2002 |
48 | Spawning release | Duirng on spawning event they spawn about 2 thousand eggs. One gram of spawn contains 1.2 thousand eggs | No category | Sczerbowski and Szczerbowski, 1996 |
49 | Parity | Reproduction occurs annually for about 6-7 years | No category | Scholfield, 2005 |
49 | Parity | Begin breeding in their second year and while they may continue to reproduce for six or seven years they yield the maximum number of eggs in their third and fourth years | No category | Battle, 1940 |
49 | Parity | They continue reproduction yearly during 6-8 years | No category | Sczerbowski and Szczerbowski, 1996 |
50 | Parental care | No, rather spawning parents often prefer to eat the new-laid eggs and hatched alevins | No care | Horvath et al, 1992 |
50 | Parental care | Non-parental | No care | Kobayashi et al, 2002 |