Trait completeness | 98% |
Total data | 407 |
References | 86 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.24-1.42 | 1.33 mm | Linhart et al, 1995 |
1 | Oocyte diameter | 1.2-1.86 | 1.53 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.5-2.1 but as small as 1.0 [Not specified if swollen] | 1.8 mm | Internet, 2005 |
1 | Oocyte diameter | 1.0-1.5 | 1.25 mm | Horvath et al, 1992 |
1 | Oocyte diameter | 1.25 | 1.25 mm | Aldridge, 1999 |
1 | Oocyte diameter | 1.5 | 1.5 mm | Lafaille and Crivelli, 2001 |
1 | Oocyte diameter | About 1.0 | 1.0 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 1.0 | 1.0 mm | Tyler and Sumpter, 1996 |
1 | Oocyte diameter | 1.20-2.00 [Average diameter of the largest oocyte in fully developed ovaries] | 1.6 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | 1.5 [Mean diameter of mature, fully yolked, ovarian oocyte] | 1.5 mm | Olden et al, 2006 |
1 | Oocyte diameter | 1.8-1.9 [Diameter of normal eggs] | 1.85 mm | Woynarovich, 1962 |
1 | Oocyte diameter | Most mature carp ovaries contained oocytes : 1.0-1.2 mm diameter | 1.1 mm | Bieniarz et al, 1979 |
1 | Oocyte diameter | The average diameter of unfertilized and unactivated eggs was 1.25 mm | 1.25 mm | Penaz et al, 1983 |
1 | Oocyte diameter | Unfertilized eggs are about 1-1.7 mm, and average 1.2-1.4 mm | 1.35 mm | Smith, 2004 |
1 | Oocyte diameter | Average diameter of unfertilized eggs immediatly after spawning was 1.2-1.6 mm (mean1.3 mm) | 1.4 mm | Matlak, 1970 |
1 | Oocyte diameter | Egg diameter in 11 month old and 23 month old carp, vary according to different king of carp from 0.79 +/- 0.025, 0.94 +/- 0.02; 1.29 +/-0.035 | 0.79 mm | Hulata et al, 1974 |
2 | Egg size after water-hardening | 1.6-1.65 = the mean size of hydrated eggs, the perivitelline space increases 5 times in diameter within 10-15 min in water | 1.62 mm | Linhart et al, 1995 |
2 | Egg size after water-hardening | 2-2.5 | 2.25 mm | Horvath et al, 1992 |
2 | Egg size after water-hardening | About 40% of swelling | 40.0 mm | Witeska et al, 1995 |
2 | Egg size after water-hardening | 1.5-1.8 [Seems to be fertilized eggs] | 1.65 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | 2.1-2.2 [Swollen] | 2.15 mm | Woynarovich, 1962 |
2 | Egg size after water-hardening | Mean diameter of swollen eggs range from: 1.875 ± 4.85 and 1.839 ± 4.38 | 1.88 mm | Kamler and Malczewski, 1982 |
2 | Egg size after water-hardening | Within 30-40 minutes this process ended and the average diameter of eggs remained at a value of 1.65 mm. [Described in other studies as: 1.5-1.8] | 1.65 mm | Penaz et al, 1983 |
2 | Egg size after water-hardening | After fertilization and swelling the diameter was 2.1-2.5 mm (mean 2.3 mm) | 2.3 mm | Matlak, 1970 |
2 | Egg size after water-hardening | Size of eggs taken from spawning beds ranged from means of 1.23 +/-0.03 to 1.76 +/-1.76 | 1.23 mm | Hulata et al, 1974 |
3 | Egg Buoyancy | Demersal | Demersal | Internet, 2005 |
3 | Egg Buoyancy | Demersal [eggs which fail to attach themselves to something will fall to the bottom of the pond and perish] | Demersal | Mickaels, 1988 |
3 | Egg Buoyancy | Demersal | Demersal | Fishbase, 2006 |
3 | Egg Buoyancy | Demersal | Demersal | Tyler and Sumpter, 1996 |
4 | Egg adhesiveness | Highly adhesive throughout incubation period | Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Adhesive | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Adhesive [Attch themselves to foliages or to roots] | Adhesive | Mickaels, 1988 |
4 | Egg adhesiveness | Adhesive | Adhesive | Lafaille and Crivelli, 2001 |
4 | Egg adhesiveness | The adhesive eggs […] become attached to submerged weeds, grasses, or roots | Adhesive | Scott and Crossman, 1973 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | Adhesive | Adhesive | Linhart et al, 2003 |
4 | Egg adhesiveness | The eggs of carp appear to be among the stickiest | Adhesive | Woynarovich, 1962 |
4 | Egg adhesiveness | Adhesive | Adhesive | Naca, 1989 |
4 | Egg adhesiveness | Adhesive | Adhesive | June, 1977 |
4 | Egg adhesiveness | Carp eggs are adhesive in water and stick to plants | Adhesive | Smith, 2004 |
4 | Egg adhesiveness | Adhesive eggs incubate on firm susbtrate including plants, dead grass, tree roots, stones, and Cladophora fronds (thalli) | Adhesive | Goodyear et al, 1982 |
4 | Egg adhesiveness | The roe was susequently rendered nonviscuous in solutions I and II (16 g tannin in 10 l water) | Non-Adhesive | Koldras and Mejza, 1983 |
4 | Egg adhesiveness | Eggs of common carp were stuck with each other and with the wall of the Petri-dish after mixing with water. Egg stikiness was fully developed within 30 s and did not increase in strength or intensity thereafter. | Adhesive | Mansour et al, 2008 |
4 | Egg adhesiveness | Egg adhesiveness was removed by immersion and shaking of the fertilized egg mass in a tannic acid solution (1g l-1) during 15 s | Adhesive | Osswald et al, 2009 |
4 | Egg adhesiveness | The adhesive chorion that occurs in these fish species allows the eggs to attach to various substrate types | Adhesive | Demsla-Zakes et al, 2005 |
5 | Incubation time | 3-4 | 3.5 days | Horvath et al, 1992 |
5 | Incubation time | 3.75 at 25°C | 3.75 days | Linhart et al, 1995 |
5 | Incubation time | 4-5 | 4.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 3-5 at 20°C | 4.0 days | Internet, 2005 |
5 | Incubation time | 6-10 [Natural conditions] | 8.0 days | Mickaels, 1988 |
5 | Incubation time | 5 days at 20°C | 5.0 days | Lafaille and Crivelli, 2001 |
5 | Incubation time | Mass hatching at 4 days at 20°C, range from 3-5.6 | 4.3 days | Witeska et al, 1995 |
5 | Incubation time | 4.0 [Mean time to egg hatch within the range of average post-spawning the range post-spawning water temperatures] | 4.0 days | Olden et al, 2006 |
5 | Incubation time | Hatching of embryos began at 51 hours and finished at an age of 57.5 hours. The peak was observed at 54 hours at 25°C | 51.0 days | Penaz et al, 1983 |
5 | Incubation time | At 20°C, the fertilized eggs of common carp take 101-104 hours to incubate, at 25°C, 49-53 hours, at 30°C, 47-50 hours | 102.5 days | Naca, 1989 |
5 | Incubation time | At 20°C carp eggs hatch after approximatively 3.5 days | 20.0 days | Smith, 2004 |
5 | Incubation time | Time from egg activation to mass hatching,in hours was: 75 [At 19.2-22.4°C], 126 [At 18-20.9°C], 171.5 [At 14.7-20.9°C] | 20.8 days | Matlak, 1970 |
5 | Incubation time | Eggs hatch in 1-3 weeks | 2.0 days | Goodyear et al, 1982 |
5 | Incubation time | They concluded that eggs laid on the marsh vegetation would normally hatch within 3-6 days after fertilization depending on water temperature | 4.5 days | Scott and Crossman, 1973 |
6 | Temperature for incubation | 15-22°C give the best results [At 10°C: a high mortality of embryos was observed, and above 25°C. the number of defective hatched individuals indreases] | 18.5 °C | Linhart et al, 1995 |
6 | Temperature for incubation | Optimal 21, range 16-26 | 21.0 °C | Saat and Veersalu, 1996 |
6 | Temperature for incubation | 20-22 | 21.0 °C | Witeska et al, 1995 |
6 | Temperature for incubation | 20-24 T for embryonic development, 12-30 range in which normal development occurs and 10 and > 33 lower and upper lethal T°C for embryonic development | 22.0 °C | Herzig and Winkler, 1986 |
6 | Temperature for incubation | The optimal temperature is from 20-24°C. In water of 17°C the eggs develop slowly and there is the danger of mould development | 22.0 °C | Woynarovich, 1962 |
6 | Temperature for incubation | Incubated at 19°C | 19.0 °C | Carvalho et al, 1997 |
6 | Temperature for incubation | Incubated at 21°C | 21.0 °C | Linhart et al, 2000 |
6 | Temperature for incubation | Eggs of each female were individually incubated in a Weiss glass at 19-20°C | 19.5 °C | Kamler and Malczewski, 1982 |
6 | Temperature for incubation | The best hatching rsults were obtained at water temperatures in the range 15-22.5°C. At higher temperatures (from 25°C)the number of defective individuals hatched increases. At a temperature of 10°C all embryos died | 18.75 °C | Penaz et al, 1983 |
6 | Temperature for incubation | Long periods of temperatures of <16°C are detrimental for embryonic development. Carp embryos are more sensitive to low temperatures than larvae. Carp larvae hatched from eggs that had been exposed to 14-17°C had shortened body trunk, curvature of tail and large unresorbed yolk sac | 15.5 °C | Matlak, 1970 |
6 | Temperature for incubation | 19°C | 19.0 °C | Osswald et al, 2009 |
6 | Temperature for incubation | The fertilized eggs from each female separately were incubated in Weiss glass in waters at 21-22°C | 21.5 °C | Brzuska and Bialowas, 2002 |
7 | Degree-days for incubation | 60-70 [At optimum incubation temperature] | 65.0 °C * day | Horvath et al, 1992 |
7 | Degree-days for incubation | 80-90 | 85.0 °C * day | Linhart et al, 1995 |
7 | Degree-days for incubation | 70 | 70.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 60-90 | 75.0 °C * day | Internet, 2005 |
7 | Degree-days for incubation | About 100 [5 days at 20°C] | 100.0 °C * day | Lafaille and Crivelli, 2001 |
7 | Degree-days for incubation | 80-100 | 90.0 °C * day | Witeska et al, 1995 |
7 | Degree-days for incubation | 30-34 [Effective day-degrees] | 32.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | In carp, the time between egg-fertilisation and hatching ranges from 60-80 degree days | 70.0 °C * day | Smith, 2004 |
2 | Egg size after water-hardening | 0.71-1.67 | 1.19 mm | Weber and Brown, 2012 |
2 | Egg size after water-hardening | 1.50-2.50 | 2.0 mm | Horvath et al, 1985 |
6 | Temperature for incubation | 22-24 | 23.0 °C | Horvath et al, 1985 |
2 | Egg size after water-hardening | 1.90 | 1.9 mm | Osse and Boogart, 1995 |
7 | Degree-days for incubation | 15.09; 6.27 | 94.61 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 17.43; 4.47 | 77.91 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 19.93; 3.47 | 69.16 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 20.46; 3.51 | 71.81 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 22.45; 2.55 | 57.25 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 24.26; 2.22 | 53.86 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 26.63; 1.83 | 48.73 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 30.44; 1.67 | 50.83 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 19.99; 4.53 | 90.55 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 19.99; 4.72 | 94.35 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 23.99; 2.55 | 61.17 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 24.02; 2.76 | 66.3 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 28.00; 1.91 | 53.48 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 28.00; 2.01 | 56.28 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 31.98; 1.52 | 48.61 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 31.98; 1.53 | 48.93 °C * day | Korwin-Kossakowski, 2008 |
7 | Degree-days for incubation | 14.51; 9.02 | 130.88 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 14.98; 6.06 | 90.78 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 18.01; 6.64 | 119.59 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 17.87; 6.06 | 108.29 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 18.95; 6.04 | 114.46 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 19.89; 4.02 | 79.96 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 20.70; 4.65 | 96.26 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 21.72; 3.64 | 79.06 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 21.79; 3.06 | 66.68 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 22.60; 3.62 | 81.81 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 23.46; 3.62 | 84.93 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 24.77; 2.53 | 62.67 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 25.11; 2.53 | 63.53 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 25.51; 2.57 | 65.56 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 25.87; 2.06 | 53.29 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 26.61; 2.03 | 54.02 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 26.92; 2.55 | 68.65 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 28.73; 2.06 | 59.18 °C * day | Silbernagel and Sorensen, 2013 |
7 | Degree-days for incubation | 30.28; 1.59 | 48.15 °C * day | Silbernagel and Sorensen, 2013 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 4.8-5.0 | 4.9 mm | Horvath et al, 1992 |
8 | Initial larval size | 4.8-5.0 | 4.9 mm | Billard et al, 1995 |
8 | Initial larval size | 4.5-5 | 4.75 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 6 [Not specified] | 6.0 mm | Linhart et al, 1995 |
8 | Initial larval size | Most average 4.38-5.70 [From 3.0 up to 6.69] | 5.04 mm | Internet, 2005 |
8 | Initial larval size | 4.7 | 4.7 mm | Aldridge, 1999 |
8 | Initial larval size | 5-6 | 5.5 mm | Lafaille and Crivelli, 2001 |
8 | Initial larval size | 4.5 | 4.5 mm | Olden et al, 2006 |
8 | Initial larval size | 4.5-5 | 4.75 mm | Wurtz-Arlet, 1950 |
8 | Initial larval size | About 5.5 [Deduced from graph] | 5.5 mm | Korwin-Kossakowski, 1988 |
8 | Initial larval size | The mean total length of embryos on hatching was 4.71 mm | 4.71 mm | Penaz et al, 1983 |
8 | Initial larval size | Total length of newly hatched larvae is 5.6-6.3 mm (mean 5.7 mm); length of head is 1.0-1.4 mm (mean 1.2 mm), body weight is about 1 mg | 5.95 mm | Matlak, 1970 |
8 | Initial larval size | Larval size of 5.5 mm immediatly after hatching | 5.5 mm | Osse et al, 1986 |
8 | Initial larval size | Average total length was 6.6 ± 0.2 mm for three-day carp larvae | 6.6 mm | Wozniewski, 1993 |
8 | Initial larval size | One day after hatching, two hundred larvae of koi (average length of 6.9 mm) | 6.9 mm | Ito et al, 2007 |
9 | Larvae behaviour | First fixed on aquatic plants then free | Demersal | Bruslé and Quignard, 2001 |
9 | Larvae behaviour | At bottom or attached to aquatic vegetation immediatly after hatching, then gradually in shallow water at bottom amon vegetation, occassionally in water column [Newly hatched larvae lay on their sides at the bottom of the aquarium] | Demersal | Internet, 2005 |
9 | Larvae behaviour | Remain fixed the first 2-3 days | Demersal | Lafaille and Crivelli, 2001 |
9 | Larvae behaviour | Immedialty after hatching the embryos remain passively on the bottom of the tank, with occasional jerly movements, and someindividuals begin to attach themselves by means of their special adhesive glands | Demersal | Penaz et al, 1983 |
9 | Larvae behaviour | After hatching, carp larvae a cement attach themselves to surface vegetation via cement glands on their head. They remain attached for 4-5 days while yolk is absorbed from a large yolk-sac and undergo organogenesis and other development | Demersal | Smith, 2004 |
9 | Larvae behaviour | Prolarvae settle to bottom immediatly after hatching and attach to plants or other objects; fry tend to leave spawning areas about 2 weeks after hatching but remain along shore among vegetation through summer | Demersal | Goodyear et al, 1982 |
10 | Reaction to light | Larvae are not photophobic | Photopositive | Mann, 1996 |
10 | Reaction to light | The basins were illuminated 24 hours | Photopositive | Wozniewski, 1993 |
11 | Temperature during larval development | 20-24 [Propagation temperature] | 22.0 °C | Horvath et al, 1992 |
11 | Temperature during larval development | Non lethal temperatures from 12.5-30, below 10 and above 32.5 all the eggs died | 21.25 °C | Geldhauser, 1995 |
11 | Temperature during larval development | 24 [Rearing conditions] | 24.0 °C | Cahu et al, 1998 |
11 | Temperature during larval development | 10-21°C | 15.5 °C | Keckeis and Schiemer, 1992 |
11 | Temperature during larval development | Reared at 25°C | 25.0 °C | Dabrowski, 1984 |
11 | Temperature during larval development | 20-24°C | 22.0 °C | Woynarovich, 1962 |
11 | Temperature during larval development | The temperature was raised from 20°C (initial hathcing temperature) to 23°C (during the experiment) | 20.0 °C | Charlon and Bergot, 1984 |
11 | Temperature during larval development | The larvae were reared at two temperatures, 20°C and 26°C, these being attained at a rate of 1°C per hour, starting from ambient hatchery temperature | 20.0 °C | Korwin-Kossakowski, 1988 |
11 | Temperature during larval development | 28-29°C for carp koi | 28.5 °C | Van Damme et al, 1989 |
11 | Temperature during larval development | The trial lasted 21 days following exogeneous feeding. Rearing temperatures was raised from 19.5°C at days 0 to 24°C at day 4 and kept at that temperature thereafter | 21.0 °C | Carvalho et al, 1997 |
11 | Temperature during larval development | In the larval period of development an increase in water temperature within the range of optimal temperatures (18-26°C) leads to to alagging behind a growth rate comperaed to development rate | 22.0 °C | Penaz et al, 1983 |
11 | Temperature during larval development | Optimum temperatures for larval growth (expressed as Relative growth rate: RGR, %d): 20-30°C | 25.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | Reared at about 26 (25-27°C) | 26.0 °C | Kamler et al, 1990 |
11 | Temperature during larval development | Reared at 20°C | 20.0 °C | Jezierska et al, 2006 |
11 | Temperature during larval development | Reared at 23°C | 23.0 °C | Osse et al, 1986 |
11 | Temperature during larval development | Reared at 21.5-22.5°C | 22.0 °C | Palikova et al, 2004 |
11 | Temperature during larval development | The water temperature was kept constant at 21 ± 1°C | 21.0 °C | Schlechtreim et al, 2004 |
11 | Temperature during larval development | The experiment was performed at a temperature of 24°C | 24.0 °C | Szlamiska, 1987 |
11 | Temperature during larval development | Water temperature was gradually raised during 24 hours, from the initial temperature of 21.0°C to the final one of 33°C | 24.0 °C | Wozniewski, 1993 |
11 | Temperature during larval development | Both strains of carp fry were fed brine shrimp until 10 days after hatching and fed commercial diet thereafter | 10.0 °C | Ito et al, 2007 |
12 | Sibling intracohort cannibalism | Cannibaslim during early life of enclosures | Absent | Dabrowski and Bardega, 1984 |
12 | Sibling intracohort cannibalism | Cannibalism as a possible cause of missing larvae (less than 7% in fed groups, less than 11% in unfed groups) was quite insufficient th explain the growth of living larvae | Present | Charlon and Bergot, 1984 |
12 | Sibling intracohort cannibalism | Sibling cannibaslim started in populations with a mean total length of c. 10.2 mm (on the 9th day after the start of exogeneous feeding) and with a cannibal to prey length ratio of 1.8 (12.9:7.2 mm). In all aquaria, cannibalism ceased when a mean total length of c. 35 mm was attained (after c. 55 days). Cannibalism was found to be positvely density-dependent | Present | Van Damme et al, 1989 |
12 | Sibling intracohort cannibalism | Cannibalism observed | Present | Bry et al, 1992 |
12 | Sibling intracohort cannibalism | Present | Present | Hecht and Pienaar, 1993 |
12 | Sibling intracohort cannibalism | Cannibalism is observed in juveniles | Present | Kozlowski and Poczyczynski, 1999 |
12 | Sibling intracohort cannibalism | Larval cannibalism was described in Koi carp, Cyprinus carpio | Present | Hatziathanasiou et al, 2002 |
13 | Full yolk-sac resorption | 60-70 | 65.0 °C * day | Billard et al, 1995 |
13 | Full yolk-sac resorption | 70 | 70.0 °C * day | Lafaille and Crivelli, 2001 |
13 | Full yolk-sac resorption | 70-80: At 25°C, the yolk has dissapeared completely between the 133th and 131st hour of development, less than 51-57.5 hours for hatching | 75.0 °C * day | Penaz et al, 1983 |
13 | Full yolk-sac resorption | For the first three days post hatching, common carp rely exclusively on endogenous food resources (yok sac). The 8-9 days old larvae have usually completely resorbed yolk sac, and feed exclusively on exogenous food | 8.5 °C * day | Jezierska et al, 2006 |
13 | Full yolk-sac resorption | It is interesing to note that the disappearance of proteolytic activity observed in the starved larvae age 10 days converges with the so-called "point of no return", which occurs on the 10th day of life of starved carp larvae at 24°C | 10.0 °C * day | Szlamiska, 1982 |
13 | Full yolk-sac resorption | Total mortality in complete absence of food in the nursing ambient occurs for common carp larvae after 9-12 days of starvation | 10.5 °C * day | Hamackova et al, 2007 |
14 | Onset of exogeneous feeding | About 100 [4 days at 26°C] | 100.0 °C * day | Khadka and Ramakrishna, 1986 |
14 | Onset of exogeneous feeding | [The larvae start to take in air and to fill the swimming bladder when about 1/2 or 2-3 of the yolk sac has been absorbed. At this time the larvae also begin to feed at 20-24°C) | 2.5 °C * day | Woynarovich, 1962 |
14 | Onset of exogeneous feeding | Larvae were fed only dry diet from the third day after hatching at 20°C | 20.0 °C * day | Charlon and Bergot, 1984 |
14 | Onset of exogeneous feeding | At the start of exogeneous feeding the mean length of the Koi carp larvae was 6.6 mm [Deduced from graph, about 3 days after hatching at 28-29°C] | 28.5 °C * day | Van Damme et al, 1989 |
14 | Onset of exogeneous feeding | 3 days after hatching with rearing temperatures was raised from 19.5°C at days 0 to 24°C at day 4 and kept at that temperature thereafter | 3.0 °C * day | Carvalho et al, 1997 |
14 | Onset of exogeneous feeding | 91 to 122 hour od development at 25°Cwe found that at a temperature of 25°C, the onset of the larval period, i.e. the intake of the first food, to take place at 91 hhours (4 day) following impregantion, wich corresponds to 37 hours (2 days after hatching) | 91.0 °C * day | Penaz et al, 1983 |
14 | Onset of exogeneous feeding | Exogenous feeding begins before the exhaustion of yolk and is marked by the taking of air to fill the swim-bladder | No data | Smith, 2004 |
14 | Onset of exogeneous feeding | Received artificial diets starting from the 3rd day after hatching (i.e. 1st day of experiment = initiation of exogeneous feeding), at about 26 (25-27°C) | 26.0 °C * day | Kamler et al, 1990 |
14 | Onset of exogeneous feeding | At 20°C, inthe series A,the 4 days old larvae captured and ingested about 70% of prey, while the 7 days old ones,over 90% | 20.0 °C * day | Jezierska et al, 2006 |
14 | Onset of exogeneous feeding | The larvae were fed by nauplii of the brine shrimp Artemia salina since the 5th day at 21.5-22.5°C | 22.0 °C * day | Palikova et al, 2004 |
14 | Onset of exogeneous feeding | First feeding (day 1 of the experiment) started 2 days after hatching when larvae exhibited an inflated swim-bladder | 1.0 °C * day | Schlechtreim et al, 2004 |
14 | Onset of exogeneous feeding | The gut evacuation time for four-day-old common carp larvae, taking their first food (Ewos C-10) is relaitvely short. It may be assumed that after 1 hour the larvae is emptied at 50% (at 24°C) | 10.0 °C * day | Szlamiska, 1987 |
8 | Initial larval size | 4.5 | 4.5 mm | Osse and Boogart, 1995 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4-5 | 4.5 year | Horvath et al, 1992 |
15 | Age at sexual maturity | 3 | 3.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 4-5 | 4.5 year | Bieniarz et al, 1978 |
15 | Age at sexual maturity | 4 | 4.0 year | Billard, ??? |
15 | Age at sexual maturity | 3 [Female] | 3.0 year | Lafaille and Crivelli, 2001 |
15 | Age at sexual maturity | 2-3 [24-36 months, age at maturation] | 2.5 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 4-5 [Females] | 4.5 year | Environment agency, ??? |
15 | Age at sexual maturity | 4.5 [Both sex] | 4.5 year | Olden et al, 2006 |
15 | Age at sexual maturity | The common carp becomes sexualy mature in the Romanian Danube River at the age of 4 years for female | 4.0 year | Ciolac, 2004 |
15 | Age at sexual maturity | Under the climatic conditions in Poland, female carp reach sexual maturity at the age of 4-5 years | 4.5 year | Bieniarz et al, 1979 |
15 | Age at sexual maturity | In temperate climates, sexual maturity is reached at the age of 3-4 years | 3.5 year | Dubost et al, 1997 |
15 | Age at sexual maturity | In tropical climates, carp mature at 3-6 months, and in temperate climates at 3-5 years. Males mature earlier than females | 4.5 year | Smith and Walker, 2004 |
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 | In Victoria, males and females mature at 1 and 2 years of age. In tropical climates, carp mature at 3-6 months. In temperate-mediterranean climates, the age-at-maturity varies between 1 and 5 years. | 4.5 year | Smith, 2004 |
16 | Length at sexual maturity | 30-40 | 35.0 cm | Horvath et al, 1992 |
16 | Length at sexual maturity | 62.5 [Both sex] | 62.5 cm | Olden et al, 2006 |
16 | Length at sexual maturity | Beetween means of 36.2 to 41.0 according to different areas for females | 36.2 cm | Ciolac, 2004 |
16 | Length at sexual maturity | In tropical climates, carp mature at 90-140 mm, and in temperate climates at 355-430 mm. Males mature earlier than females. In the present study the majority of fish in the lower Murray are mature by 350 mm | 115.0 cm | Smith and Walker, 2004 |
17 | Weight at sexual maturity | 4-5 | 4.5 kg | Horvath et al, 1992 |
17 | Weight at sexual maturity | 3-5 [But 0.8-1 in France] | 4.0 kg | Billard, ??? |
17 | Weight at sexual maturity | Females of 5 years, 3-4 kg were used | 3.5 kg | Bieniarz et al, 1979 |
18 | Female sexual dimorphism | For female carp, they include the softening and enlargement of the abdomen and the reddening and protrusion of the cloaca | Present | Smith, 2004 |
19 | Relative fecundity | 100-300 | 200.0 thousand eggs/kg | Linhart et al, 1995 |
19 | Relative fecundity | 80-150 | 115.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 100-200 | 150.0 thousand eggs/kg | Horvath et al, 1992 |
19 | Relative fecundity | 100-300 | 200.0 thousand eggs/kg | Billard, ??? |
19 | Relative fecundity | 120-180 | 150.0 thousand eggs/kg | Lafaille and Crivelli, 2001 |
19 | Relative fecundity | 100-200 | 150.0 thousand eggs/kg | Environment agency, ??? |
19 | Relative fecundity | 100 | 100.0 thousand eggs/kg | Kunz, 2004 |
19 | Relative fecundity | Different means vary between 290 to 588 | 290.0 thousand eggs/kg | Banbura and Koszalinski, 1991 |
19 | Relative fecundity | Estimates of instantaneous fecundity (the average number of strippd eggs per kilogram of fish) ranged from 114,000 to 163,000 eggs per kg | 114.0 thousand eggs/kg | Smith, 2004 |
20 | Absolute fecundity | 200-1500 | 850.0 thousand eggs | Horvath et al, 1992 |
20 | Absolute fecundity | 36-2208 | 1122.0 thousand eggs | Internet, 2005 |
20 | Absolute fecundity | 190.778-375.000 in four different populations [Average number of vitellogenic oocyes of mature females in a single spawning season] | 282.89 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
20 | Absolute fecundity | Average of 85 | 85.0 thousand eggs | Ciolac, 2004 |
20 | Absolute fecundity | The average fecundity of a 3-year-old, 44-48 cm, 1.9-2.75 kg, common carp is around 224,000 pieces. For a 5-year-old, 54 cm, 3.5 kg common carp, the fecundity is around 447,000 pieces. | 46.0 thousand eggs | Naca, 1989 |
20 | Absolute fecundity | The females are highly fecund and depending on body size, produce between 500,000 and 3 million eggs per spawning | 500.0 thousand eggs | Smith, 2004 |
20 | Absolute fecundity | Eggs numbers ranging from 36,000 eggs in a 15.5-inch (394 mm) fish to 2,208,000 eggs in a 33.5 inch (851 mm) fish. The latter weighed 22.23 pounds (10.1 kg) | 36.0 thousand eggs | Scott and Crossman, 1973 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
21 | Oocyte development | Asynchronous | Asynchronous | Bruslé and Quignard, 2001 |
21 | Oocyte development | Carp ovary development is asynchronous | Asynchronous | Dubost et al, 1997 |
21 | Oocyte development | Common carp are asynchronous, multiple batch spawners with indeterminate breeding season fecunidty. At the individual level, oocytes at all developmental stages occurred in some ovaries, but discrete batches of oocytes typically matured in synchrony. Not all eggs from the same batch were necessarily spawned at once, and it is likely that some fish spawned again within weeks (one individual retained a portion of mature oocytes in the anterior of each ovary after spawning). | Asynchronous | Smith and Walker, 2004 |
22 | Onset of oogenesis | GSI increased gradually from August until February | ['January', 'February', 'August', 'September', 'October', 'November'] | Yaron and Levavi-Zermonsky, 1986 |
22 | Onset of oogenesis | June-July | ['June', 'July'] | Bieniarz et al, 1978 |
22 | Onset of oogenesis | October | ['October'] | Crivelli, 1981 |
22 | Onset of oogenesis | January [In Australia] | ['January'] | Smith and Walker, 2004 |
22 | Onset of oogenesis | GSI increase from 1.7 +/- 0.4 in September 28 to 6.2 +/- 1.1 in November 12 for big-belly and 0.4 +/-0.1 to 1.1 +/- 0.2 for Gold in Israel | ['September', 'November'] | Hulata et al, 1974 |
23 | Intensifying oogenesis activity | October to December | ['October', 'November', 'December'] | Yaron and Levavi-Zermonsky, 1986 |
23 | Intensifying oogenesis activity | October to November | ['October', 'November'] | Bieniarz et al, 1978 |
23 | Intensifying oogenesis activity | A dramatic growth is observed in April | ['April'] | Crivelli, 1981 |
23 | Intensifying oogenesis activity | September [In Australia] | ['September'] | Smith and Walker, 2004 |
24 | Maximum GSI value | 20-30 | 25.0 percent | Bruslé and Quignard, 2001 |
24 | Maximum GSI value | About 10% | 10.0 percent | Yaron and Levavi-Zermonsky, 1986 |
24 | Maximum GSI value | Mean of 28%, up to 30% [June] | 28.0 percent | Crivelli, 1981 |
24 | Maximum GSI value | Maximum GSI values in female 17%, less than in other studies 29% | 17.0 percent | Dubost et al, 1997 |
24 | Maximum GSI value | Mean of 18% up to 21-22% [In October in Australia] | 21.5 percent | Smith and Walker, 2004 |
24 | Maximum GSI value | About 25% [May] | 25.0 percent | June, 1977 |
24 | Maximum GSI value | Recorded estimates are usually around 20% for males | 20.0 percent | Smith, 2004 |
25 | Oogenesis duration | 3-4 [August until December] | 3.5 months | Yaron and Levavi-Zermonsky, 1986 |
26 | Resting period | Few weeks after spawning | No data | Bieniarz et al, 1978 |
26 | Resting period | About two months [June-July] | 3.0 months | Yaron and Levavi-Zermonsky, 1986 |
26 | Resting period | About 5% in December-January | 5.0 months | Smith and Walker, 2004 |
26 | Resting period | Almost 0 [July] | 2.0 months | Yaron and Levavi-Zermonsky, 1986 |
26 | Resting period | Post-spawning period: June-August | 3.0 months | Bieniarz et al, 1979 |
26 | Resting period | July and august are a quiescent period of gonadal activity; a stage of regeneration | 2.0 months | Crivelli, 1981 |
26 | Resting period | Re-maturation of the ovaries requires > 3-4 months | 3.5 months | Smith, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2-3 | 2.5 years | Horvath et al, 1992 |
27 | Age at sexual maturity | 2-3 | 2.5 years | Billard, ??? |
27 | Age at sexual maturity | 2 | 2.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2 [Male] | 2.0 years | Lafaille and Crivelli, 2001 |
27 | Age at sexual maturity | 4.5 [Both sex] | 4.5 years | Olden et al, 2006 |
27 | Age at sexual maturity | The common carp becomes sexualy mature in the Romanian Danube River at the age of 3 years for male | 3.0 years | Ciolac, 2004 |
27 | Age at sexual maturity | In temperate climates, for males, spawning occurs during the second or third year of life | 2.0 years | Dubost et al, 1997 |
27 | Age at sexual maturity | In Victoria, males and females mature at 1 and 2 years of age. On average males mature one year earlier than females | 1.0 years | Smith, 2004 |
28 | Length at sexual maturity | 25-30 | 27.5 cm | Horvath et al, 1992 |
28 | Length at sexual maturity | 62.5 [Both sex] | 62.5 cm | Olden et al, 2006 |
28 | Length at sexual maturity | Between means of 28.9 to 34.9 according to different areas for males | 28.9 cm | Ciolac, 2004 |
28 | Length at sexual maturity | Individuals studied were 56.3 ± 1 and 54.2 ± 0.7 | 56.3 cm | Belova, 1981 |
29 | Weight at sexual maturity | 3-4 | 3.5 kg | Horvath et al, 1992 |
29 | Weight at sexual maturity | 1 [0.5 in France] | 1.0 kg | Billard, ??? |
29 | Weight at sexual maturity | Individuals studied were 1.930 ±124 and 1.907 ± 113 | 1.93 kg | Belova, 1981 |
30 | Male sexual dimorphism | Develop pimples on the gills | Present | Mickaels, 1988 |
30 | Male sexual dimorphism | Males bear nuptial tubercles on head and body | Present | Lafaille and Crivelli, 2001 |
30 | Male sexual dimorphism | Nuptial tubercles fine and scattered | Present | Scott and Crossman, 1973 |
30 | Male sexual dimorphism | The abdomen of male carp does not become obviously distended but may become darker in colour and nuptial tubercles appear on the head and on pectoral fin rays | Present | Smith, 2004 |
31 | Onset of spermatogenesis | Spermatogenesis occur in summer and spermatozoa are found in the testis in autumn | ['July', 'August', 'September', 'October', 'November', 'December'] | Billard et al, 1995 |
31 | Onset of spermatogenesis | August | ['August'] | Crivelli, 1981 |
31 | Onset of spermatogenesis | January in Australia | ['January'] | Smith and Walker, 2004 |
32 | Main spermatogenesis activity | August-September, then increase slowly until March | ['March', 'August', 'September'] | Crivelli, 1981 |
32 | Main spermatogenesis activity | January in Australia | ['January'] | Smith and Walker, 2004 |
33 | Maximum GSI value | 7 | 7.0 percent | Suquet et al, 1994 |
33 | Maximum GSI value | 6.9 ± 2.6 | 6.9 percent | Saad and Billard, 1987 |
33 | Maximum GSI value | Range between 10.62 and 11.97 for individuals studied but not specified if the maximum and the date | 10.62 percent | Belova, 1981 |
33 | Maximum GSI value | Mean of 8.2, up to 9.2 [Beginning of April] | 8.2 percent | Crivelli, 1981 |
33 | Maximum GSI value | Maximum GSI for males 11% less than in other studies 15% | 11.0 percent | Dubost et al, 1997 |
33 | Maximum GSI value | About 7% in March in Australia | 7.0 percent | Smith and Walker, 2004 |
33 | Maximum GSI value | Recorded estimates are usually around 10% for males | 10.0 percent | Smith, 2004 |
33 | Maximum GSI value | GSI reaches 16.3 +/- 2.0 for big-belly and 7.0 +/- 0.7% for Gold in November 12 in Israel | 16.3 percent | Hulata et al, 1974 |
34 | Spermatogenesis duration | Spermiogenesis is very short in carp [the completion of spermatogenesis is in october] | No data | Billard et al, 1995 |
34 | Spermatogenesis duration | Although the spermatogenesis is continuous there is a male gonadal cycle which increases in September and decreases around May | 3.0 months | Crivelli, 1981 |
34 | Spermatogenesis duration | Spermatogenesis was continuous and spermatogonia, psermatocytes, spermatids and sperm co-occurred in most testes throughout the spawning and non-spawning periods. Thus, males are euipped to spawn at any time during the year, but there is a defined gonadal cycle with a peak in Ig before the onset of spawning | No data | Smith and Walker, 2004 |
35 | Resting period | Lower in december-January, about 2% | 2.0 months | Smith and Walker, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Localised spawning migrations | No data | Environment agency, ??? |
36 | Spawning migration distance | Move from littoral waters into marshes beginning in April or early May at about 45°F; also ascend tributaries, usually only short distances, but sometimes as far as 10-15 mi | 12.5 km | Goodyear et al, 1982 |
37 | Spawning migration period | The carp migration usually starts in April when the water temperature is about 12°C and it has the highest intensity in May when the water temperature is aournd 16°C. The water temperature of 18°C to 20°C is the optimum for spawning. | ['April', 'May'] | Ciolac, 2004 |
37 | Spawning migration period | Adults move into weedy and grassy shallows | No data | Scott and Crossman, 1973 |
37 | Spawning migration period | In the spring, when water temperatue is about 10-14°C | ['April', 'May', 'June'] | Ciolac, 2004 |
39 | Spawning season | April-June | ['April', 'June'] | Horvath et al, 1992 |
39 | Spawning season | May-June | ['May', 'June'] | Billard, 1997 |
39 | Spawning season | March to July [Peak spawning in May through July] | ['March', 'April', 'May', 'June', 'July'] | Internet, 2005 |
39 | Spawning season | May-July [March-August] | ['March', 'May', 'June', 'July', 'August'] | Bruslé and Quignard, 2001 |
39 | Spawning season | May | ['May'] | Bieniarz et al, 1978 |
39 | Spawning season | May-July | ['May', 'July'] | Lafaille and Crivelli, 2001 |
39 | Spawning season | Carp spawn in the spring and summer […] | ['April', 'May', 'June', 'July', 'August', 'September'] | Scott and Crossman, 1973 |
39 | Spawning season | May-July | ['May', 'July'] | Mann, 1996 |
39 | Spawning season | May-July | ['May', 'July'] | Environment agency, ??? |
39 | Spawning season | May-July | ['May', 'July'] | Herzig and Winkler, 1986 |
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 | The spawning of carp in the Camargue begins in March and ens generally in August: for Europe this is the longest known spawing period | ['March', 'August'] | Crivelli, 1981 |
39 | Spawning season | Mean peak spawning 27 May [Range: 21 April - 26 June] in Lake Oahe, South and North Dakota | ['April', 'May', 'June'] | June, 1977 |
39 | Spawning season | The studies were conducted in experimental ponds at the Fish and Aquaculture Research station, Dor. All the fish spawned within a single week in April. | ['April'] | Hulata et al, 1974 |
39 | Spawning season | May-August at 52-90°F; peak spawning occurs in late Mat-early June at 65-73°F; spawning may extend throughout summer subject to interruption by cool weather | ['May', 'June', 'July', 'August', 'September'] | Goodyear et al, 1982 |
39 | Spawning season | In May, the natural spawning period for this fish species | ['May'] | Brzuska and Bialowas, 2002 |
40 | Spawning period duration | Spawning may continue for several weeks […] Spawning is usually extended when water temperatures permit and in the Great Lakes region may extend from May to August | No data | Scott and Crossman, 1973 |
40 | Spawning period duration | 4-26 [1.00-6.00 months, length of breeding season] | 15.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
40 | Spawning period duration | Duration of spanwing of carp from different areas: March to August [Camargue, France], Mid-March to August [scutari Lake, Y.U.], Mid-April to July [Terek delta, U.S.S.R], Mid-April to August [Danube Delta, Rou.], May to July [St-Lawrence Lake, Canada], May-June [South Dakota, U.S.A] | No data | Crivelli, 1981 |
40 | Spawning period duration | Longest recorded period for common carp spawning in Australia. It continued from mid-november 2001 to mid-May 2002 (7 months), and recommnced in mid-september 2002 | 2001.0 weeks | Smith and Walker, 2004 |
41 | Spawning temperature | 18-22 is the optimum [Peaking at 22-26, but from 15-28°] | 20.0 °C | Internet, 2005 |
41 | Spawning temperature | 16-22 | 19.0 °C | Horvath et al, 1992 |
41 | Spawning temperature | 20-22 | 21.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 18 | 18.0 °C | Bieniarz et al, 1978 |
41 | Spawning temperature | Above 18 | 18.0 °C | Lafaille and Crivelli, 2001 |
41 | Spawning temperature | Spawning does not commence in earnest until temperatures reach a level of at least 62.6°F (17°C) and may continue for several weeks. Spawning activities begin to decline when temperatures reach 78.8°F (26°C) and cease altogether at 82.4°F (28°C). In lake St. Lawrence, it was observed that spawning may be interrupted if cooler wheather prevails and the temperature drops below 62.6°F (17°C), but will recommence when the water warms up again | 62.6 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | 15-20 | 17.5 °C | Fishbase, 2006 |
41 | Spawning temperature | 16-22 | 19.0 °C | Mann, 1996 |
41 | Spawning temperature | 16-22 | 19.0 °C | Environment agency, ??? |
41 | Spawning temperature | 16-22 | 19.0 °C | Herzig and Winkler, 1986 |
41 | Spawning temperature | 17 [Temperature at which spawning is typically initiated] | 17.0 °C | Olden et al, 2006 |
41 | Spawning temperature | 18-20 | 19.0 °C | Kamler et al, 1996 |
41 | Spawning temperature | The water temperature of 18°C to 20°C is the optimum for spawning | 18.0 °C | Ciolac, 2004 |
41 | Spawning temperature | Begins when water temperature reaches 18°C, although cases are reported of females spawning at lower temperature e.g., 14°C | 18.0 °C | Bieniarz et al, 1979 |
41 | Spawning temperature | A temperature around15-16°C | 15.5 °C | Crivelli, 1981 |
41 | Spawning temperature | Minimum temperature 15-16 [Camargue, France]; 15.5-17 [Scutari Lake], 17 [Terek delta], 16-18 [St-Lawrence, Lake, Canada], 16.6-20 [South dakota, U.S.A.] | 15.5 °C | Crivelli, 1981 |
41 | Spawning temperature | Although the spawning season begins at different times, water temperature requirements are identical, at least 18°C | 18.0 °C | Naca, 1989 |
41 | Spawning temperature | Spawning is low from 15-18°C, optimum 18-23°C, and ceases at 28°C | 16.5 °C | Smith, 2004 |
42 | Spawning water type | Tidal and non-tidal fresh water, either in fresh water or oligohaline water (10 ppt) | No category | Internet, 2005 |
42 | Spawning water type | Flooding areas if available | No category | Lafaille and Crivelli, 2001 |
42 | Spawning water type | Weedy and grassy shallows | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Spawn in marginal, shallow, weed-infested areas | Stagnant water | Fishbase, 2006 |
42 | Spawning water type | Stagnant water or with a weak flow | Stagnant water | Belova, 1981 |
42 | Spawning water type | A shallow flooded area | No category | Crivelli, 1981 |
42 | Spawning water type | Fish spawning out of the tributary area: carp, pikeperch, catfish Silurus glanis and eel | No category | Hladik and Kubecka, 2003 |
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 | Preferred spawning sites are lentic habitats with abundant food, warm water and protection from predators | No category | Smith, 2004 |
42 | Spawning water type | Protected areas of lakes and rivers, including bays, harbors, marshes, sloughs, flooded shorelines, and river mouths; also on shoals and reefs | Stagnant water | Goodyear et al, 1982 |
43 | Spawning depth | Shallow areas, near surface | No data | Internet, 2005 |
43 | Spawning depth | Shallow areas | No data | Lafaille and Crivelli, 2001 |
43 | Spawning depth | Shallow | No data | Fishbase, 2006 |
43 | Spawning depth | Shallow areas | No data | Crivelli, 1981 |
43 | Spawning depth | The spawning act occurs in shoreline areas (water < 1 m deep) | 1.0 m | Smith, 2004 |
43 | Spawning depth | To 20 Ft, but usually less than 3 feet, and often 3 inches-1 feet | 20.0 m | Goodyear et al, 1982 |
43 | Spawning depth | Many an early morning, the bass fisherman, casting into weedy shallows, has been startled by the sudden arrival of one or more groups of spawning carp | No data | Scott and Crossman, 1973 |
44 | Spawning substrate | Submerged plants, grass roots of undercut tanks, dead leaves, floating plants and logs | Phytophils | Internet, 2005 |
44 | Spawning substrate | Phytophil : aquatic plants | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Weedy areas | Phytophils | Internet, 2005 |
44 | Spawning substrate | Foliage or roots | No category | Mickaels, 1988 |
44 | Spawning substrate | Aquatic plants | Phytophils | Lafaille and Crivelli, 2001 |
44 | Spawning substrate | Submerged weeds, grasses or roots | Phytophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Obligatory plant spawners | Phytophils | Fishbase, 2006 |
44 | Spawning substrate | Phytophils: eggs adhere to submerged macrophytes, <5 cm in diamter | Phytophils | Mann, 1996 |
44 | Spawning substrate | Deposit their eggs on plants | Phytophils | Kennedy, 1969 |
44 | Spawning substrate | Dense weed, bulrushes | Phytophils | Environment agency, ??? |
44 | Spawning substrate | Phytophils | Phytophils | Balon, 1975 |
44 | Spawning substrate | Phytophils | Phytophils | Kamler et al, 1996 |
44 | Spawning substrate | Member of the phytophilous group | Phytophils | Belova, 1981 |
44 | Spawning substrate | Abundant and fixed vegetation (macrophytes, red or even in the Camargue sansouire) | Phytophils | Crivelli, 1981 |
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 | Scattered thair adhesive eggs on vegetation in the littoral zone of tributary embayments | Phytophils | June, 1977 |
44 | Spawning substrate | Obligatory plant spawners | Phytophils | Smith, 2004 |
44 | Spawning substrate | Eggs are broadcast at random near the surface over mud, muck, silt, sand, matted roots or dead grass, and abundant emergent, submergent, and floating vegetation; also over gravel, rock and rubble | Lithophils | Goodyear et al, 1982 |
45 | Spawning site preparation | No | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Eggs are deposited randomly | Susbtrate chooser | Scott and Crossman, 1973 |
45 | Spawning site preparation | Open water/substratum eggs scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Mann, 1996 |
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 |
45 | Spawning site preparation | Not any male spawning territory | No category | Ah-King et al, 2004 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Kamler et al, 1996 |
45 | Spawning site preparation | Open-substratum | No category | Smith, 2004 |
46 | Nycthemeral period of oviposition | Ovulation and spawing usually occur between midnight and early morning | Day | Aida, 1988 |
46 | Nycthemeral period of oviposition | Dawn and less in dusk | Dawn | Bruslé and Quignard, 2001 |
46 | Nycthemeral period of oviposition | Courtship starts early in the morning, about 6-7 am and finishes about noon | Day | Mickaels, 1988 |
46 | Nycthemeral period of oviposition | Dawn | Dawn | Lafaille and Crivelli, 2001 |
46 | Nycthemeral period of oviposition | Warm sunny morning | Day | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | Spawning occurred mainly early in the morning until 10.00 hours, although some carp were observed just before the sunset | Day | Crivelli, 1981 |
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 |
46 | Nycthemeral period of oviposition | Spawning occurs during daylight | Day | Smith, 2004 |
47 | Mating system | One female and several males | Polyandry | Bruslé and Quignard, 2001 |
47 | Mating system | Usually a female will be accompanied by 2 or 3 males | No category | Scott and Crossman, 1973 |
47 | Mating system | Polygamous: a female is usually followed by several males | No category | Fishbase, 2006 |
47 | Mating system | Group: communal spawning, several males pursue female for some time before spawning | Promiscuity | Ah-King et al, 2004 |
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 |
47 | Mating system | Spawning involves polygamous groups of one female and several males and is apparently triggered, at certain times of the year, by rising water that inundates terrestrial vegetation and periods of fine, warm weather | Polyandry | Smith, 2004 |
48 | Spawning release | Able to spawn more than once during the breeding season | Multiple | Internet, 2005 |
48 | Spawning release | Eggs are released in two or three times over a period of 10-14 days | No category | Bruslé and Quignard, 2001 |
48 | Spawning release | Sometimes several batches | Multiple | Lafaille and Crivelli, 2001 |
48 | Spawning release | Deposited in clusters, repeated deposition | Fractional | Internet, 2005 |
48 | Spawning release | Single spawning per year | Total | Vila-Gispert and Moreno-Amich, 2002 |
48 | Spawning release | Multiple spawning | Multiple | Environment agency, ??? |
48 | Spawning release | Carp may spawn repeatedly during the same year if environmental conditions are favourable. Multiple maturation was confirmed by histological analysis | Multiple | Dubost et al, 1997 |
48 | Spawning release | As long as conditions are met, and there is appropriate habitat, common carp will spawn repeatedly. Thus, common carp in tropical fresh waters are perennial spawners, and females annually release four to five discrete batches of eggs. | Multiple | Smith and Walker, 2004 |
48 | Spawning release | Carp are fractional spawners with indeterminate breeding season fecundity. Depending on local thermo and photo conditions, each female may spawn one to five batches of eggs per year. In India, carp spawn once. In southern France, Bengladesh, and west Bengal they may spawn twice. In tropical climates, carp are perennial spawners and spawn 4-5 times per year | Multiple | Smith, 2004 |
49 | Parity | Iteroparous; one cycle/year when reared in an outside natural pond [but up to five if maintained at 20-24°C] | Iteroparous | Linhart et al, 1995 |
49 | Parity | Iteroparous | Iteroparous | Bruslé and Quignard, 2001 |
49 | Parity | In Victoria, estimates of longetivy range between 15-40 years | No category | Smith, 2004 |
49 | Parity | Disperse after spawning but remain in shallows throughout the summer; | No category | Goodyear et al, 1982 |
50 | Parental care | Not described in that review | No category | Scott and Crossman, 1973 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |
50 | Parental care | Non-guarding | No care | Smith, 2004 |