Trait completeness | 78% |
Total data | 146 |
References | 20 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 0.62-1.34 [Egg diameter in ovarium: ripe with yolk] | 0.98 mm | Holopainen, 1997 |
1 | Oocyte diameter | 1-1.5 | 1.25 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.3-1.7 | 1.5 mm | Persat, 2001 |
1 | Oocyte diameter | 1.4-1.7 [Not specified] | 1.55 mm | Fishbase, 2006 |
1 | Oocyte diameter | Crucian carp eggs just before spawning have 0.8-1.2 mm in diameter. They are much larger than the eggs from the anterior part of the ovary, which are depostied later; before the first spawning they have 0.2-0.7 mm in diameter. Detailed observations and measurements revealed that the diameter of the eggs from the polder Novo-Marievskij was 0.91, 0.98, 0.93, 0.80-0.91 and 0.90 mm in March, April, May, June and August, respectively, mean egg diameter in the population studied was 0.903 mm | 1.0 mm | Sczerbowski and Szczerbowski, 1996 |
1 | Oocyte diameter | The eggs of crucian carp are spherical and yellowish-orange. The diameter of the eggs were 1.37 mm (SD = 0.09, n = 62) in HL 1.61 mm (SD = 0.10, n = 62) in Varaslampi. […] Other author give a diameter of 1.05-1.35 mm for mature oocytes (eggs) of crucian carps in West Siberian waters. Also describes as 1.45-1.52 mm. | 1.2 mm | Laurila and Holopainen, 1990 |
2 | Egg size after water-hardening | 1-2 [Fertilized eggs] | 1.5 mm | Holopainen, 1997 |
2 | Egg size after water-hardening | After fertilization the eggs swell | No data | Laurila and Holopainen, 1990 |
3 | Egg Buoyancy | Demersal | Demersal | Holopainen, 1997 |
3 | Egg Buoyancy | Demersal [On the bottom] | Demersal | Fishbase, 2006 |
4 | Egg adhesiveness | Adhere to submerged plants | Adhesive | Holopainen, 1997 |
4 | Egg adhesiveness | Adhere to submerged plants | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | Adhere to plants | Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive | Adhesive | Naca, 1989 |
4 | Egg adhesiveness | The eggs attach singly to the vegetation | Non-Adhesive | Laurila and Holopainen, 1990 |
5 | Incubation time | 6 [18-19°C], < 3 days [24-28°C] | 18.5 days | Holopainen, 1997 |
5 | Incubation time | 3-7 | 5.0 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 4-8 [6 days at 18.5°C] | 6.0 days | Fishbase, 2006 |
5 | Incubation time | Eggs incubate during 4-7 days | 5.5 days | Sczerbowski and Szczerbowski, 1996 |
5 | Incubation time | The incubation depends on temperature being approx. 4 days at 20°C and 2 days at 25-27°C | 26.0 days | Laurila and Holopainen, 1990 |
6 | Temperature for incubation | Develop normaly at 15-28 [Die at 5, 10 and 30°] | 21.5 °C | Holopainen, 1997 |
6 | Temperature for incubation | 24-28, temperature for the shortest embryonic development [Eggs hatched normally at 15-28°C, but died at 5-10, and above 30°C] | 26.0 °C | Laurila et al, 1987 |
6 | Temperature for incubation | 18.5°C | 18.5 °C | Fishbase, 2006 |
6 | Temperature for incubation | Placed in jars kept at room temperature (20-25°C) | 22.5 °C | Laurila and Holopainen, 1990 |
6 | Temperature for incubation | Different stages of embryonic, larval and juvenile development were described from fish kept at 20°C in the laboratory | 20.0 °C | Laurila and Holopainen, 1990 |
7 | Degree-days for incubation | 80-110 [i.e. 6 days at 18-19°C, and < 3 days at 24-28°C] | 95.0 °C * day | Holopainen, 1997 |
7 | Degree-days for incubation | 80-100 [6 days at 18-19°C in natural conditions, or 3 days at 24-28°C] | 90.0 °C * day | Laurila et al, 1987 |
7 | Degree-days for incubation | 29 [Effective day-degrees] | 29.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | 95-100 | 97.5 °C * day | Sczerbowski and Szczerbowski, 1996 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 4.5-5.5 | 5.0 mm | Holopainen, 1997 |
8 | Initial larval size | 4 | 4.0 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 4.5-5.5 | 5.0 mm | Laurila et al, 1987 |
8 | Initial larval size | Length of newly hatched larvae is about 5 mm, body mass 10 mg | 5.0 mm | Szczerbowski and Szczerbowski, 1996 |
8 | Initial larval size | The total length of the larva is 4.5-5.5 mm at hatching. Other authors: 5.0-5.2 ; 4.2-4.9 ; 3.8-5.2 | 5.0 mm | Laurila and Holopainen, 1990 |
9 | Larvae behaviour | In nature, the free embryo are passive and often attach themselves to plants, where they stay hiding for the first 1-2 days of the endogenous feeding period | Demersal | Laurila et al, 1987 |
9 | Larvae behaviour | Eggs are deposited on plants to which they remain fixed during endogeneous feeding | Demersal | Szczerbowski and Szczerbowski, 1996 |
9 | Larvae behaviour | The newly hatched larvae are passive: they lie on the bottom of the aquarium, for example. In the second day after hatching they try to swimupwards, towards the light (positive phototaxis) and attach to plants | Demersal | Laurila and Holopainen, 1990 |
10 | Reaction to light | Larvae are not photophobic | Photopositive | Mann, 1996 |
10 | Reaction to light | Positive phototaxis | Photopositive | Laurila and Holopainen, 1990 |
11 | Temperature during larval development | 20-25, maximum size obtained and highest yolk utilization efficiency [At 5°C, no increase but the larvae were deformed and all died after 8 days] | 22.5 °C | Laurila et al, 1987 |
11 | Temperature during larval development | Reared at 22°C | 22.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | Different stages of embryonic, larval and juvenile development were described from fish kept at 20°C in the laboratory | 20.0 °C | Laurila and Holopainen, 1990 |
13 | Full yolk-sac resorption | At 20 and 25°C, a maximum size of 7.6 mm, and at 30°C, 7.4 mm was achieved. The survival time (50% mortality) on yolk sac energy was 8 days both at 5 and 25-30°C, 9 days at at 20°C, and 14 days at 10-14°C. Even when Artemia nauplii were available on the fourth day, feeding (food in the gut) was noted at 15°C only, but its importance even here is not known since all died at the embryonic stage | 27.5 °C * day | Laurila et al, 1987 |
13 | Full yolk-sac resorption | The yolk sac disappears completely at the length between 6.5-7.2 mm | 6.85 °C * day | Laurila and Holopainen, 1990 |
14 | Onset of exogeneous feeding | When food are available from the start, larvae began mixed feeding at lengths of 6.5-7.2 mm, after 2-4 days of development at 20-30°C, when much of the yolk was present | 6.85 °C * day | Laurila et al, 1987 |
14 | Onset of exogeneous feeding | A few days (3 days at 20°C) after hatching the fish swim to the surface to fill the swim bladder and then switch to exogenous feeding and yolk reserves are reduced. | 3.0 °C * day | Laurila and Holopainen, 1990 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | From 2 to 4 according to latitudes | 2.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3-4 [Not specified] | 3.5 year | Environment agency, ??? |
15 | Age at sexual maturity | 2-5 [Not specified] | 3.5 year | Scholfield, 2005 |
15 | Age at sexual maturity | In the Changjiang River and Yellow River basins, generally reach maturity at 2 years. In northeastern China, sexual maturity arrives later when the fish is larger | 2.0 year | Naca, 1989 |
15 | Age at sexual maturity | Crucian carp mature at the age of 3-5 years, usually 4 years. Typically males mature a year earlier than females. Maturation is reached earlier in the regions situated near the sourthern limit of the distribution area. In Roumania fish maturing in their second year of life were observed, whereas in Northern Russia - in fifth. Because of better nutritional conditions in ponds, maturation is earlier than in natural water bodies | 4.0 year | Sczerbowski and Szczerbowski, 1996 |
16 | Length at sexual maturity | 11-13 | 12.0 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | Mean of females range from 11.69 ± 2.2 (range 7.8-19.1) in Pond Hermanninlampi, and 32.86 ± 6.2 (range 14.9-39.7) and 23.39-+/ 2.3 (range 19.3-27.5) in lake Varaslampi | 11.69 cm | Aho and Holopainen, 2000 |
17 | Weight at sexual maturity | 0.085-0.100 | 0.09 kg | Bruslé and Quignard, 2001 |
17 | Weight at sexual maturity | Mean of females range from 31.2 ±20 g in Pond Hermanninlampi, and 933.3 ± 339.4 and 311.7 ± 100.1 in lake Varaslampi | 31.2 kg | Aho and Holopainen, 2000 |
18 | Female sexual dimorphism | The head and scales develop tubercules in the epithelium | Absent | Holopainen, 1997 |
18 | Female sexual dimorphism | During the spawning season, both males and females developped small tubercles in the epithelium when ready to spawn. At both sites some sexual dimorphism was observed. In males, the tubercles were most abundant, covering both head and body, but in females they were limited to the head region only. Nearly all ripe male crucian carps had tubercles. At the beginning of the reproudction period, tubercles covered only the head (forehead and operculum); but a few days later they were found on the body as well. In female fish the tubercles were found only on teh head and tuberculum. by the end of the ripe period tubercles were absent in both sexes | Absent | Aho and Holopainen, 2000 |
19 | Relative fecundity | 150-240 | 195.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | Fecundity varies with age, body length and, above all, with body mass. Females age 3+ to 7+ produce 16 460 eggs on the average,which is equivalent to about 163 eggs per g of body mass. Relative fecundity was very variable: 15-700 thousand eggs per kg of body mass. | 357.5 thousand eggs/kg | Sczerbowski and Szczerbowski, 1996 |
20 | Absolute fecundity | 100-250 | 175.0 thousand eggs | Persat, 2001 |
20 | Absolute fecundity | 100-250 per females | 175.0 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | 130-250 per female | 190.0 thousand eggs | Fishbase, 2006 |
20 | Absolute fecundity | 22-24 | 23.0 thousand eggs | Wisniewolski, 1988 |
20 | Absolute fecundity | A 0.5-1 kg crucian carp has an average fecundity of 200,00 - 300,000 pieces | 0.75 thousand eggs | Naca, 1989 |
20 | Absolute fecundity | Fecundity varies with age, body length and, above all, with body mass. Females age 3+ to 7+ produce 16 460 eggs on the average,which is equivalent to about 163 eggs per g of body mass. Also described as for females of of 18-22 cm long, ranged from 137 to 224 thousand eggs. In Poland absolute fecudity of crucian carp females reached maximally 400 000 eggs per female, but is is usually much lower. In the lake Pogorzelisko fish (size: 11-21 cm and 34-320 g) produced 0.7-81-5 thousand eggs per female. Fecundity of crucian carp females of similar length (11.0-20.2 cm) and mass (53-313 g) from the lake Girijal ranged from 5-155.6 thousand, and that of females from the lake Ilmen (body mass 278-500 g) ranged from 137-207 thousand eggs, from which the first batch contained 24.0-90.4 thousand eggs | 20.0 thousand eggs | Sczerbowski and Szczerbowski, 1996 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
21 | Oocyte development | Non-synchronous maturation | No category | Bruslé and Quignard, 2001 |
21 | Oocyte development | Asynchronous | Asynchronous | Papadopol and Weinberger, 1975 |
24 | Maximum GSI value | About 20% | 20.0 percent | Bruslé and Quignard, 2001 |
24 | Maximum GSI value | GSI range from an average of 5.51 ± 1.36 (range 3.92-7.91); to 8.59 ± 1.80 (range 5.60-11.8), and 11.56 ± 5.78 (range 3.63-20.98) in three fifferent regions in May | 5.51 percent | Aho and Holopainen, 2000 |
24 | Maximum GSI value | Total mass of eggs related to body mass ranged from 11.7-20.3%, which is much higher than the data of other authors (0.9-12.8%) | 16.0 percent | Sczerbowski and Szczerbowski, 1996 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3-4 [Not specified] | 3.5 years | Environment agency, ??? |
27 | Age at sexual maturity | 2-5 [Not specified] | 3.5 years | Scholfield, 2005 |
28 | Length at sexual maturity | Mean of males range from 8.95 ± 1.8 (range 6.3-15.2) in Pond Hermanninlampi, and 28.90 ± 5.5 (range 13.9-35.7) and 23.28-+/ 4.6 (range 14.8-28.5) in lake Varaslampi | 8.95 cm | Aho and Holopainen, 2000 |
29 | Weight at sexual maturity | Mean of males range from 10.5 ±6.1 g in Pond Hermanninlampi, and 640.2 ± 288.7 and 302.7 ± 137.2 in lake Varaslampi | 10.5 kg | Aho and Holopainen, 2000 |
30 | Male sexual dimorphism | The head and scales develop tubercules in the epithelium | Absent | Holopainen, 1997 |
30 | Male sexual dimorphism | Nuptial tubercules on head and first rays of fins | Present | Spillmann, 1961 |
30 | Male sexual dimorphism | Male bears nuptial tubercules over the head, opercules, and first rays of pectoral fins | Present | Bruslé and Quignard, 2001 |
30 | Male sexual dimorphism | Male bears nuptial tubercules over the head, opercules, and first rays of pectoral fins | Present | Billard, 1997 |
30 | Male sexual dimorphism | Males generally mature one year earlier | Absent | Scholfield, 2005 |
30 | Male sexual dimorphism | Thre is a popular belief that crucian carp have no externally visible secondary or tertiary sexual dimorphisms. However, several authors report on higher weight of females than males at same length. Females live longer than males in the same environment. | Absent | Sczerbowski and Szczerbowski, 1996 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Localised spawning migrations | No data | Environment agency, ??? |
36 | Spawning migration distance | No migration | No data | Agence de l'eau, |
36 | Spawning migration distance | Crucian carp are considered to be non-migratory fish. In spring, they move from deeper part of water bodies toshallower parts which are warmer and better endowed with oxygen. Crucian carp move slowly. In autumn they return to deeper waters | No data | Sczerbowski and Szczerbowski, 1996 |
39 | Spawning season | March-June | ['March', 'June'] | Billard, 1997 |
39 | Spawning season | June-July | ['June', 'July'] | Spillmann, 1961 |
39 | Spawning season | From late spring trough mid-summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Holopainen, 1997 |
39 | Spawning season | May-June, April-June [Southern Region] | ['April', 'May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | Starts in May-June and and continues in summer | ['May', 'June', 'July', 'August', 'September'] | Persat, 2001 |
39 | Spawning season | May-June | ['May', 'June'] | Mann, 1996 |
39 | Spawning season | May-June | ['May', 'June'] | Environment agency, ??? |
39 | Spawning season | May-June | ['May', 'June'] | Fishbase, 2006 |
39 | Spawning season | Spawn from the end of March to early April in Central and central eastern part of China, from April to May in Northern China, and in June on northeastern China. | ['March', 'April', 'May', 'June'] | Naca, 1989 |
39 | Spawning season | Spawn in May, June and July. Peak of spawning occurs between 20 May and 20 July, depending on geographic position | ['May', 'June', 'July'] | Sczerbowski and Szczerbowski, 1996 |
39 | Spawning season | Between May and July | ['May', 'July'] | Laurila and Holopainen, 1990 |
40 | Spawning period duration | >2 months [including spawning and hatching] | 2.0 weeks | Holopainen, 1997 |
40 | Spawning period duration | Up to 4 | 4.0 weeks | Persat, 2001 |
40 | Spawning period duration | The ready-to-spawn (ripe) fish (n=430) were captured between 19 May and 21 July, all within 64 days. In other sites: 32 dats and 60 days | 430.0 weeks | Aho and Holopainen, 2000 |
41 | Spawning temperature | 17-20 | 18.5 °C | Holopainen, 1997 |
41 | Spawning temperature | 15-20 | 17.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | >16 | 16.0 °C | Persat, 2001 |
41 | Spawning temperature | 14-22 | 18.0 °C | Mann, 1996 |
41 | Spawning temperature | Above 18 | 18.0 °C | Scholfield, 2005 |
41 | Spawning temperature | Spawning is not likely to occur until the water temperature reaches 17-20°C, especially in harsh climatic conditions as those in Finland | 18.5 °C | Aho and Holopainen, 2000 |
41 | Spawning temperature | Although the spawning season begins at different times, water temperature requirements are identical, at least 20°C | 20.0 °C | Naca, 1989 |
41 | Spawning temperature | Spawning begins at temperature > 14°C | 14.0 °C | Sczerbowski and Szczerbowski, 1996 |
41 | Spawning temperature | The spawning of this species takes place at high temperatures (> 17°C) | 17.0 °C | Laurila and Holopainen, 1990 |
42 | Spawning water type | Ponds | Stagnant water | Laurila et al, 1987 |
42 | Spawning water type | Naturally reproduce in the still or running waters of Southern and Nothern China | No category | Naca, 1989 |
42 | Spawning water type | Near-shore parts of water bodies | Stagnant water | Sczerbowski and Szczerbowski, 1996 |
43 | Spawning depth | Shallow areas of ponds | No data | Laurila et al, 1987 |
43 | Spawning depth | Shallow water | No data | Fishbase, 2006 |
43 | Spawning depth | Shallow water | No data | Sczerbowski and Szczerbowski, 1996 |
44 | Spawning substrate | Phytophilous, open substrates submerged twigs and macrophytes | Phytophils | Holopainen, 1997 |
44 | Spawning substrate | Phytophilous : submerged plants | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Phytophil | Phytophils | Persat, 2001 |
44 | Spawning substrate | Plant substrate | Phytophils | Laurila et al, 1987 |
44 | Spawning substrate | Phytophils: eggs adhere to submerged macrophytes | Phytophils | Mann, 1996 |
44 | Spawning substrate | Dense marginal weed | Phytophils | Environment agency, ??? |
44 | Spawning substrate | Dense vegetation | Phytophils | Fishbase, 2006 |
44 | Spawning substrate | Phytophils | Phytophils | Balon, 1975 |
44 | Spawning substrate | Vegetation | Phytophils | Scholfield, 2005 |
44 | Spawning substrate | The fundamental requirement for spawning is the presence of susbstrat (e.g. aquatic plants) that the eggs can adhere to | Phytophils | Naca, 1989 |
44 | Spawning substrate | Overgrown with vegetation | Phytophils | Sczerbowski and Szczerbowski, 1996 |
44 | Spawning substrate | The species is described as being phytophil, open substrate spawner | Phytophils | Laurila and Holopainen, 1990 |
45 | Spawning site preparation | No, eggs are laid on plant susbtrates | Susbtrate chooser | Laurila et al, 1987 |
45 | Spawning site preparation | Open water/susbtratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Release over vegetation | No category | Scholfield, 2005 |
45 | Spawning site preparation | The species is described as being phytophil, open substrate spawner | Susbtrate chooser | Laurila and Holopainen, 1990 |
46 | Nycthemeral period of oviposition | Preferentially during the morning | Day | Bruslé and Quignard, 2001 |
46 | Nycthemeral period of oviposition | Mating itself is likely to take place at night or early in the morning, whencrucian carps are known to be most active | Day | Aho and Holopainen, 2000 |
46 | Nycthemeral period of oviposition | Spawning activity proceeds from midnight to dawn. If environmental conditions are favourable, however, these fish can spawn the whole day | Day | Naca, 1989 |
47 | Mating system | In estrus, two or three males chase one female; the male repeatedly hits its head against the female's abdomen until the female is lying on its side adjacent to some aquatic plants. | No category | Naca, 1989 |
48 | Spawning release | Multiple | Multiple | Rinchard, 1996 |
48 | Spawning release | Three periods of spawnings have been commoly observed from late May to mid-July, with female producing similar number of eggs | Multiple | Holopainen, 1997 |
48 | Spawning release | Multiple (fractional) spawner | Multiple | Laurila et al, 1987 |
48 | Spawning release | Intermittent spawners, eggs are deposited in temporally discrete batches | Multiple | Holopainen, 1997 |
48 | Spawning release | Fractionnal spawner : 4 to 5 spawning during a period of 10-15 days [Polycycle] | No category | Bruslé and Quignard, 2001 |
48 | Spawning release | Up to three spawning periods between late May and early August | Multiple | Laurila et al, 1987 |
48 | Spawning release | Batch spawner | Multiple | Scholfield, 2005 |
48 | Spawning release | Crucian carp is one of the batch-spawning cyrpinids fround in nothern Europe | Multiple | Aho and Holopainen, 2000 |
48 | Spawning release | Spawn in 3-5 batches during each summer | Multiple | Sczerbowski and Szczerbowski, 1996 |
48 | Spawning release | The eggs are laid in 2-3 batches […] This species is a fractional spawner: the females release only part of their eggs at each spawning | Multiple | Laurila and Holopainen, 1990 |
49 | Parity | The maximum lifespan of wild crucian carp is about 10 years | No category | Scholfield, 2005 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |