Trait completeness | 96% |
Total data | 226 |
References | 36 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.375-1.625 [Ova] | 1.5 mm | Kennedy and Fitzmaurice, 1972 |
1 | Oocyte diameter | 1.5-2 | 1.75 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 2 [Not specified] | 2.0 mm | Spillmann, 1961 |
1 | Oocyte diameter | 1.2 | 1.2 mm | Rossechi and Kestemont, 2001 |
1 | Oocyte diameter | 1.4-1.8 | 1.6 mm | Fishbase, 2006 |
1 | Oocyte diameter | 1.126 [Mean egg size, not specified] | 1.13 mm | Rosecchi et al, 2001 |
1 | Oocyte diameter | 1.2 | 1.2 mm | Tyler and Sumpter, 1996 |
1 | Oocyte diameter | 0.73-1.76, up to 2.20 ? [Average diameter of the largest oocyte in fully developed ovaries] | 1.25 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | 1.8 [Not specified] | 1.8 mm | Copp et al, 2002b |
1 | Oocyte diameter | Non-inseminated, freshly stripped gudgeon eggs are 0.99 mm in diameter | 0.99 mm | Penaz and Prokes, 1978 |
1 | Oocyte diameter | Unfertilized and not swollen fish eggs measured 1.24 mm on average, with the mean range from 1.17 to 1.32 mm (and their mass averaged 0.70 mg; 0.67 to 0.78) | 1.24 mm | Palikova and Krejci, 2006 |
2 | Egg size after water-hardening | Mainly 1.3, varying between 1.3-1.35 [Drifting eggs] | 1.33 mm | Copp et al, 2002b |
2 | Egg size after water-hardening | At water temperature of 19°C, the water uptake lasted about 45 minutes and the eggs increased their diameter to 1.29 mm | 1.29 mm | Penaz and Prokes, 1978 |
2 | Egg size after water-hardening | 1.5 [Not specified] | 1.5 mm | Kamler and Wolnicki, 2006 |
2 | Egg size after water-hardening | Fertilized fish eggs in a swollen stated had 1.51 mm (1.42-1.62) in diameter and their mass was 1.48 mg on average (1.22-1.87) | 1.52 mm | Palikova and Krejci, 2006 |
2 | Egg size after water-hardening | Les œufs sont blancs tanslucides et mesurent 1.4 à 1.8 mm de diamètre (moyenne 1.5 mm); ceci rejoint les observations en Irlande où les œufs de goujons mesurent de 1.30 à 1.65 mm | 1.8 mm | Brunet and Hoestlandt, 1972 |
3 | Egg Buoyancy | Demersal | Demersal | Kennedy and Fitzmaurice, 1972 |
3 | Egg Buoyancy | Demersal | Demersal | Tyler and Sumpter, 1996 |
4 | Egg adhesiveness | Adhesive | Adhesive | Spillmann, 1961 |
4 | Egg adhesiveness | Adhesive [Eggs adhere to pebbles, weeds, tree roots and sodden leaves] | Adhesive | Kennedy and Fitzmaurice, 1972 |
4 | Egg adhesiveness | Adhesive | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Slightly adhesive | Adhesive | Rinchard, 1996 |
4 | Egg adhesiveness | Adhesive | Adhesive | Billard, 1997 |
4 | Egg adhesiveness | Highly adhesive | Adhesive | Rossechi and Kestemont, 2001 |
4 | Egg adhesiveness | Sticky | Adhesive | Penaz and Prokes, 1978 |
4 | Egg adhesiveness | Fish eggs were unsticked enzymatically using alcalase for three minutes | Adhesive | Palikova and Krejci, 2006 |
4 | Egg adhesiveness | Les œufs pondus adhérent aux graviers | Non-Adhesive | Brunet and Hoestlandt, 1972 |
5 | Incubation time | 14-28 | 21.0 days | Spillmann, 1961 |
5 | Incubation time | 5-6 at 20°C | 5.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 7-8 days at 17.5°C | 7.5 days | Kennedy and Fitzmaurice, 1972 |
5 | Incubation time | In the Mohelno locality, it lasted 7 days at daily mean water temperature of 16.9°C and in laboratory, 150 hours (5days) at 19.5°C. At mean water temperature of 20.14°C, the first embryos hatched in the 190th hour of development, i.e. on the 5th days after insemination of the eggs. Hatcing ended in the 164th hour of development, i.e., on the 7th day after insemination of the eggs. Other authors: 8.5 daysat 16°C, 8 days at 17.5°Cand 6 at 18°C | 7.0 days | Penaz and Prokes, 1978 |
5 | Incubation time | The hatching of eggs from females not treated hormonally started on average 71 hours after fertilization with the range of 66 to 79 hours. Most eggs hatched within 39 hours from the start of hatching. All embryos hatched within 136 hours after fertilization. | 71.0 days | Palikova and Krejci, 2006 |
5 | Incubation time | 6 days at 20°C | 6.0 days | Brunet and Hoestlandt, 1972 |
6 | Temperature for incubation | 17-18 | 17.5 °C | Kennedy and Fitzmaurice, 1972 |
6 | Temperature for incubation | 20°C | 20.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | Artificially inseminated eggs were incubated on Petri dishes at water temperatures varying between 18.1 and 20.5°C | 18.1 °C | Penaz and Prokes, 1978 |
6 | Temperature for incubation | Fish eggs were incubated at 21 ± 0.3°C | 21.0 °C | Palikova and Krejci, 2006 |
6 | Temperature for incubation | 19-20°C | 19.5 °C | Brunet and Hoestlandt, 1972 |
7 | Degree-days for incubation | 125.0 | 125.0 °C * day | Rinchard, 1996 |
7 | Degree-days for incubation | 125.0 | 125.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 120-140 [7-8 days at 17.5°C] | 130.0 °C * day | Kennedy and Fitzmaurice, 1972 |
7 | Degree-days for incubation | The mean duration of incubation was 133.4 DD at 20.4°C, also described at 6 days at 20°C (125 DD) | 133.4 °C * day | Penaz and Prokes, 1978 |
7 | Degree-days for incubation | 125°D | 125.0 °C * day | Brunet and Hoestlandt, 1972 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 5.45 | 5.45 mm | Kennedy and Fitzmaurice, 1972 |
8 | Initial larval size | 4-5 | 4.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 4.5-5.5 | 5.0 mm | Rinchard, 1996 |
8 | Initial larval size | 4.7 | 4.7 mm | Chemillier, 1995 |
8 | Initial larval size | 3.0-4.2 | 3.6 mm | Penaz and Prokes, 1978 |
8 | Initial larval size | Mean of 4.3 (4 to 4.7 mm). […] In Ireland, length of 4.68 to 5.45 mm | 4.7 mm | Brunet and Hoestlandt, 1972 |
9 | Larvae behaviour | Tend to keep to the bottom. where they rest upright with the spread out of their pectoral fins | Demersal | Kennedy and Fitzmaurice, 1972 |
9 | Larvae behaviour | Benthic larvae | Demersal | Mann, 1996 |
9 | Larvae behaviour | The hatched embryos mostly lie still on the bottom | Demersal | Penaz and Prokes, 1978 |
10 | Reaction to light | Benthic larvae are photophobic | Photophobic | Mann, 1996 |
11 | Temperature during larval development | 20-25 [At 28 optimal growth but problem with anoxia and pathology] | 22.5 °C | Chemillier, 1995 |
11 | Temperature during larval development | 18-20 | 19.0 °C | Kennedy and Fitzmaurice, 1972 |
11 | Temperature during larval development | Reared at 20°C | 20.0 °C | Wolnicki, 2005 |
12 | Sibling intracohort cannibalism | Not any cannibalism has ever been observed | Absent | Chemillier, 1995 |
13 | Full yolk-sac resorption | 90-100 [5 days at 18-20°C] | 95.0 °C * day | Kennedy and Fitzmaurice, 1972 |
13 | Full yolk-sac resorption | La vésicule est résorbée en quatre jours (à + 20°C) et les alevins de notre élevage mesurent 5.15 (5 à 5.5 mm) alors que l'alevin d'Irlande atteint 6 mm | 20.0 °C * day | Brunet and Hoestlandt, 1972 |
14 | Onset of exogeneous feeding | 60 [3 days at 18-20°C] | 19.0 °C * day | Kennedy and Fitzmaurice, 1972 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2-3 [Both sex] | 2.5 year | Kennedy and Fitzmaurice, 1972 |
15 | Age at sexual maturity | 3 | 3.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 2 [Sometimes 1, rarely 3-4, Box sex] | 3.5 year | Rosechhi and Kestemont, 2001 |
15 | Age at sexual maturity | 2-3 [Female] | 2.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 1 [Bot sex] | 1.0 year | Rosecchi et al, 2001 |
15 | Age at sexual maturity | 1-2 [12-24 months, age at maturation] | 1.5 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 2-3 [Not specified] | 2.5 year | Environment agency, ??? |
15 | Age at sexual maturity | Nearly all fish were mature at the end of their third year, and approximatively 89% from females and 74% Stour females spawnerd after two years | 3.0 year | Mann, 1980 |
15 | Age at sexual maturity | Celle-ci peut-être atteinte dès le second été (1+) chez les groupes qui mesurent 90 à 100 mm de longueur. […] 50% seulement des femelles de goujons 1+ sont aptes à se reproduire. Toutes les femelles 2+ sont aptes à la reproduction | 2.0 year | Brunet and Hoestlandt, 1972 |
16 | Length at sexual maturity | 7.9 is the smallest mature female | 7.9 cm | Kennedy and Fitzmaurice, 1972 |
16 | Length at sexual maturity | 8-10 | 9.0 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | 9.3 [Female] | 9.3 cm | Fishbase, 2006 |
16 | Length at sexual maturity | 5.5 | 5.5 cm | Rosecchi et al, 2001 |
16 | Length at sexual maturity | Female were mature at 9.29 in Stour | 9.29 cm | Mann, 1980 |
16 | Length at sexual maturity | Mean of 11.04, range 8.5-13.6 for females studied | 11.05 cm | Banbura and Koszalinski, 1991 |
17 | Weight at sexual maturity | Gudgeon generally reaches a size of 8-10 cm and a weight of 10 g at 2 years, 12-13 cm and 20-25 g at 3 years | 9.0 kg | Kestemont and Mélard, ??? |
18 | Female sexual dimorphism | Tubercles are present mostly on the head, and in the largest individuals also on scales of back | Present | Witkowski and Rogowska, 1991 |
19 | Relative fecundity | 180-849 | 514.5 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 200-250: 500-4500 [Age 2, weight 10g], 1500-9000 [Age 3, 20-25 g] | 225.0 thousand eggs/kg | Kestemont and Mélard, 1994 |
20 | Absolute fecundity | 1-3 | 2.0 thousand eggs | Spillmann, 1961 |
20 | Absolute fecundity | 0.5-15 | 7.75 thousand eggs | Rinchard, 1996 |
20 | Absolute fecundity | 4.8-20.8 [Great Britain] and 0.5-3 [France] | 12.8 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 1.987-3.240 for three populations up to 15.950 in England [Average number of vitellogenic oocyes of mature females in a single spawning season] | 2.61 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
20 | Absolute fecundity | 2.5-6.5 | 4.5 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | Mean number of eggs per fish in successive age groups: 4812 [Age 2]; 9787 [Age 3], 15950 {Age 4]; 20823 [Age 5] in Frome; 5044 [Age 3], 4472 [Age 4], and 6781 [Age 5] in Thames; 500 [Age 2], 1500 [Age 3]; 3000 [Age 4] and 4-5000 [Age 6] in Nivelle; 1721 [Age 3]; 2053 [Age 4], 2886 [Age 5]; 3585 [Age 6]; 5610 [Age 7] in Dunajec | 2502.0 thousand eggs | Mann, 1980 |
20 | Absolute fecundity | Mean of 4 643, range 629-14 600 | 321.5 thousand eggs | Banbura and Koszalinski, 1991 |
20 | Absolute fecundity | Categorized as between 2000 and 100000 eggs per reproductive cycle | 2000.0 thousand eggs | Cattanéo et al, 2001 |
20 | Absolute fecundity | 500-4500 [Age 2], 1500-9000 [Age 3], 3000-15000 [Age 4] | 2500.0 thousand eggs | Kestemont and Mélard, 1994 |
20 | Absolute fecundity | On peut admettre que la femelle agée de 1+ pond 500 œufs, celle de 2+ 15000, celle de 3+ 3000 et celle de 5+ 4000 à 5000 | 1.0 thousand eggs | Brunet and Hoestlandt, 1972 |
21 | Oocyte development | Between group-synchronous and synchronous | Group-synchronous | Rinchard, 1996 |
21 | Oocyte development | Asynchronous oocyte development | Asynchronous | Rinchard et al.. General and Comparative Endocrinology 92. 168-178 (1993) |
21 | Oocyte development | Asynchronous | Asynchronous | Bruslé and Quignard, 2001 |
21 | Oocyte development | Asynchonous | Asynchronous | Kestemont, 1987 |
21 | Oocyte development | Develops oocyes asynchronously | Asynchronous | Kestemont, 1990 |
21 | Oocyte development | Développement asynchrone | Asynchronous | Beelen et al, 1998/1999 |
22 | Onset of oogenesis | Mid-October [Greatly decreased between November to April] | ['January', 'February', 'March', 'April', 'October', 'November'] | Kestemont, 1987 |
22 | Onset of oogenesis | October to March slight increase from 3 to 4.59 | ['January', 'February', 'March', 'October', 'November'] | Rinchard et al, 1993 |
22 | Onset of oogenesis | Increase in October | ['October'] | Mann, 1980 |
22 | Onset of oogenesis | In October, all fishes were at the same stage of development and only contained stage 1 and 2 ooctyes. Stage 3, reached in November, continued until April as the most advanced stage. | ['April', 'October', 'November'] | Kestemont, 1990 |
23 | Intensifying oogenesis activity | May | ['May'] | Kestemont, 1987 |
23 | Intensifying oogenesis activity | April-May | ['April', 'May'] | Rinchard et al, 1993 |
23 | Intensifying oogenesis activity | April [From 6.3 in March to 17.6 in April] | ['March', 'April'] | Rosecchi et al, 2001 |
23 | Intensifying oogenesis activity | April | ['April'] | Mann, 1980 |
23 | Intensifying oogenesis activity | Enlargement of ooctyes by accumulation of yolk globules caused a marked increase in GSI in May | ['May'] | Kestemont, 1990 |
24 | Maximum GSI value | 16.53 ± 1.53 [Idem as Spawning value, May-June] | 16.53 percent | Rinchard et al, 1993 |
24 | Maximum GSI value | 23-28.6 | 25.8 percent | Bruslé and Quignard, 2001 |
24 | Maximum GSI value | 16.5% [June, and July] | 16.5 percent | Kestemont, 1987 |
24 | Maximum GSI value | 17.1 [April, May] | 17.1 percent | Rosecchi et al, 2001 |
24 | Maximum GSI value | Huge variations between females, from 4 to 22, most between 12-18% in May | 15.0 percent | Mann, 1980 |
24 | Maximum GSI value | 13.5 [End of May in the control group] | 13.5 percent | Kestemont, 1990 |
25 | Oogenesis duration | 9-10 [October to June] | 9.5 months | Kestemont, 1987 |
26 | Resting period | 1-2 [August-September] | 1.5 months | Kestemont, 1987 |
26 | Resting period | 2-3 [From July through September] | 2.5 months | Rinchard et al, 1993 |
26 | Resting period | < 3.10 ± 1.53 (July-August-September] | 3.1 months | Rinchard et al, 1993 |
26 | Resting period | About 3% [August, September] | 3.0 months | Kestemont, 1987 |
26 | Resting period | From July, the ovary started a recovery phase and only contained stage 1 and 2 ooctyes. One ot two months of quiscence following summer spawning | 1.0 months | Kestemont, 1990 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2-3 [Both sex] | 2.5 years | Kennedy and Fitzmaurice, 1972 |
27 | Age at sexual maturity | 2 | 2.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2 [Sometimes 1, rarely 3-4, Box sex] | 3.5 years | Rosechhi and Kestemont, 2001 |
27 | Age at sexual maturity | 2-3 [male] | 2.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 1 [Bot sex] | 1.0 years | Rosecchi et al, 2001 |
27 | Age at sexual maturity | 3-4 [Males] | 3.5 years | Environment agency, ??? |
27 | Age at sexual maturity | 2-3 [Not specified] | 2.5 years | Environment agency, ??? |
27 | Age at sexual maturity | Nearly all fish were mature at the end of their third year, and approximatively 64% of all males after two years | 3.0 years | Mann, 1980 |
28 | Length at sexual maturity | 6.9 is the smallest male | 6.9 cm | Kennedy and Fitzmaurice, 1972 |
28 | Length at sexual maturity | 9.70-10.50 [Male] | 10.1 cm | Fishbase, 2006 |
28 | Length at sexual maturity | Mean size of mature males 10.46 cm in Frome and 9.66 cm in Stour | 10.46 cm | Mann, 1980 |
30 | Male sexual dimorphism | During the spawning season, male bears nuptial tubercules | Present | Spillmann, 1961 |
30 | Male sexual dimorphism | At spawning time, the heads of ripe male are thickly sprinkled with small nuptial tubercles like those of the dace. Nuptial tubercules also occur on the pectoral fins | Present | Kennedy and Fitzmaurice, 1972 |
30 | Male sexual dimorphism | Bears nuptial tubercules | Present | Bruslé and Quignard, 2001 |
30 | Male sexual dimorphism | During the spawning season, male bears nuptial tubercules on head and opercules | Present | Rinchard, 1996 |
30 | Male sexual dimorphism | In males, tubercles are much more intensively developped than in females. In larger individuals, the whole head, trunk, and all the fins are covered by tubercules [only head for smallest] | Absent | Witkowski and Rogowska, 1991 |
30 | Male sexual dimorphism | Male bears nuptial tubercles on head | Present | Billard, 1997 |
30 | Male sexual dimorphism | During the spawning season, male bears nuptial tubercules | Present | Rossechi and Kestemont, 2001 |
31 | Onset of spermatogenesis | From December increase regularly | ['December'] | Kestemond, 1989 |
31 | Onset of spermatogenesis | Developed gradually through the winter | ['January', 'February', 'March'] | Mann, 1980 |
32 | Main spermatogenesis activity | May and mid-June | ['May', 'June'] | Kestemond, 1989 |
32 | Main spermatogenesis activity | Increased rapidly in size just prior to spawning in late May and early June | ['May', 'June'] | Mann, 1980 |
33 | Maximum GSI value | 2.3 [June, prior to spawning] | 2.3 percent | Kestemond, 1989 |
33 | Maximum GSI value | 2.3 [During the breeding season] | 2.3 percent | Rosecchi et al, 2001 |
33 | Maximum GSI value | Huge variations between individuals: mostly 1-3% in May | 2.0 percent | Mann, 1980 |
34 | Spermatogenesis duration | During autumn and finish at the end of spring | 7.0 months | Kestemond, 1989 |
35 | Resting period | 0.9 [September to October] | 3.0 months | Kestemond, 1989 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Limited home range | No data | Environment agency, ??? |
39 | Spawning season | May-June | ['May', 'June'] | Billard, 1997 |
39 | Spawning season | Mid-April until End of August, with a peak in May-June | ['April', 'May', 'June', 'August'] | Rinchard, 1996 |
39 | Spawning season | April-May to June-July and Mid-August | ['April', 'May', 'June', 'July', 'August'] | Bruslé and Quignard, 2001 |
39 | Spawning season | April to June [France] | ['April', 'May', 'June'] | Kennedy and Fitzmaurice, 1972 |
39 | Spawning season | May-June | ['May', 'June'] | Spillmann, 1961 |
39 | Spawning season | April to July [Peak in May-june] | ['April', 'May', 'June', 'July'] | Rosechhi and Kestemont, 2001 |
39 | Spawning season | May-July | ['May', 'July'] | Mann, 1996 |
39 | Spawning season | April-July | ['April', 'July'] | Rosecchi et al, 2001 |
39 | Spawning season | April-August | ['April', 'August'] | Environment agency, ??? |
39 | Spawning season | Spawn in France between April and May. In the Don River, spawning was observed at the turn of April and May. In the waters of Ireland, spawn from lata May till late June | ['April', 'May', 'June'] | Penaz and Prokes, 1978 |
39 | Spawning season | (April) May-June | ['April', 'May', 'June'] | Kamler and Wolnicki, 2006 |
39 | Spawning season | May-June | ['May', 'June'] | Cattanéo et al, 2001 |
39 | Spawning season | In the Trent, the main hatching period for gudgeon was between late May and mid-June, with smaller numbers of fish from subsequent cohorts appearing at intervals therefater | ['May', 'June'] | Nunn et al, 2007 |
39 | Spawning season | Pond au printemps et en été […] elle variera donc selon la latitude, l'altitude et les différences annuelles des températures printanières […] C'est ainsi que dans les Dombes, la ponte peut commencer dès la seconde quinzaine d'avril alors que dans la Montagne Noire il faut attendre la seconde quinzaine de juin ou même le début de juillet. La période de ponte s'échève début juin dans les eaux relativement chaudes alors qu'elle peut durer jusqu'en septembre dans les eaux froides. Dans le Sud de l'Angleterre, la ponte peut débuter en fin avril (Tamise); mais en Irlande, elle ne commencera qu'en mai ou en juin | No data | Brunet and Hoestlandt, 1972 |
40 | Spawning period duration | 4-8 | 6.0 weeks | Bruslé and Quignard, 2001 |
40 | Spawning period duration | 4-8 [A female spawns about 4 times, with an interval of 1-2 weeks between each] | 6.0 weeks | Kestemont, 1987 |
40 | Spawning period duration | 4-16 [1.00-4.00 month, length of breeding season] | 10.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
40 | Spawning period duration | In 1976: 11-13 May, at a mean watre temperature of 15.4 to 16.4°C; 17-19 May, at 15.1-16.4°C, 25-27 May, at 14.5-16.5°C and 10-12 June at 13.6 to 16.0°C | 12.0 weeks | Penaz and Prokes, 1978 |
41 | Spawning temperature | 14-17 [But sometimes 12°C] | 15.5 °C | Kennedy and Fitzmaurice, 1972 |
41 | Spawning temperature | Ovulation requires a temperature of 16-17 [Optimum 20°C] | 16.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 14-17 | 15.5 °C | Rinchard, 1996 |
41 | Spawning temperature | 16-17 is the minimum required | 16.5 °C | Kestemont, 1987 |
41 | Spawning temperature | Above about 15°C | 15.0 °C | Rosechhi and Kestemont, 2001 |
41 | Spawning temperature | 12-17 | 14.5 °C | Mann, 1996 |
41 | Spawning temperature | 17 and more | 17.0 °C | Environment agency, ??? |
41 | Spawning temperature | Spawning occurred at daily mean temperature of 13.6 to 16.5°C. Based on all studies, it could be concluded that spawning occurs most frequently in May and June at water temperatures between 15 and 18°C | 13.6 °C | Penaz and Prokes, 1978 |
41 | Spawning temperature | 12-17 | 14.5 °C | Kamler and Wolnicki, 2006 |
41 | Spawning temperature | La température de l'eau était comprise entre 22 et 24°C et la photopériode fixée à 16L/8N | 22.0 °C | Poncin et al, 1997 |
41 | Spawning temperature | La date des premières pontes annuelles est essentiellement dépendante de la température de l'eau (+ 16 à + 17°C); | 16.0 °C | Brunet and Hoestlandt, 1972 |
42 | Spawning water type | Rivulet of about 30 cm wide; canal of 2 m wide | Stagnant water | Kennedy and Fitzmaurice, 1972 |
42 | Spawning water type | Slow-flowing current : 10 to 80 cm/s | Flowing or turbulent water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Water with some current | Flowing or turbulent water | Spillmann, 1961 |
42 | Spawning water type | Current velocity: 2-80 cm/s | Flowing or turbulent water | Mann, 1996 |
42 | Spawning water type | Dans une eau faiblement courante | Flowing or turbulent water | Brunet and Hoestlandt, 1972 |
43 | Spawning depth | 5 to 8 cm deep and 40-50 cm deep | 45.0 m | Kennedy and Fitzmaurice, 1972 |
43 | Spawning depth | Shallow waters | No data | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Plants or gravels | Lithophils | Spillmann, 1961 |
44 | Spawning substrate | Pebbles, weeds, tree roots and sodden leaves | Lithophils | Kennedy and Fitzmaurice, 1972 |
44 | Spawning substrate | Psmanophile: sand, pebbles and small pebbles but sometimes aquatic plants | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Psmanophil: sand or gravels | Lithophils | Rinchard, 1996 |
44 | Spawning substrate | Gravels and plants | Lithophils | Billard, 1997 |
44 | Spawning substrate | Clean gravel and vegetation in flowing water | Lithophils | Fishbase, 2006 |
44 | Spawning substrate | Eggs are laid on sand or fine roots associated with sand, washed by running water | Pelagophils | Mann, 1996 |
44 | Spawning substrate | Lithophil | Lithophils | Kennedy, 1969 |
44 | Spawning substrate | Gravel, typically 10-20 mm | Lithophils | Environment agency, ??? |
44 | Spawning substrate | Psammophil | Psammophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Psammophils | Psammophils | Balon, 1975 |
44 | Spawning substrate | Psammophil | Psammophils | Cattanéo et al, 2001 |
44 | Spawning substrate | Si nos résultats préliminaires sur le goujon tendaient à se confirmer, il deviendrait intéressant de discuter le caractère psammophile de la reproduction de cette espèce | Psammophils | Poncin et al, 1997 |
44 | Spawning substrate | Sur un fond de gravier ou de cailloutis […] Accessoirement les œufs peuvent être pondus, partiellement au moins, sur les végétaux immergés des rives du cours d'eau. Il est probable que les œufs qui tombent sur un fond vaseux sont perdus, car en aquarium, on constate que des oeufs reposant sur le fond (verre ou sable) ne se développent pas | No category | Brunet and Hoestlandt, 1972 |
45 | Spawning site preparation | No | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Open water/susbtratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | No, eggs are laid on substrate [Open substratum spawners] | Susbtrate chooser | 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 | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
45 | Spawning site preparation | Ce comportement a pour effet de libérer les œufs dans la colonne d'eau | No category | Poncin et al, 1997 |
46 | Nycthemeral period of oviposition | Night | Night | Spillmann, 1961 |
46 | Nycthemeral period of oviposition | Le goujon pond normalement au début de la nuit | Night | Brunet and Hoestlandt, 1972 |
47 | Mating system | Si nos observations sont confirméesnle mode de reproduction du goujon pourrait être considéré comme polygame, chaque femelle étant suceptible de se reproduire avec plusieurs mâles successivement, voire même simultanément, et chaque mâle pouvant se reproduire successivement avec des femelles différentes | No category | Poncin et al, 1997 |
48 | Spawning release | Frationnal and multiple spawner | Multiple | Chemillier, 1995 |
48 | Spawning release | Frationnal and multiple spawner | Multiple | Rossechi and Kestemont, 2001 |
48 | Spawning release | Batch spawner [Spawns once a year in low productivity streams, but exhibits multiple spawinng within a season in high productivity environments] | Multiple | Fishbase, 2006 |
48 | Spawning release | By batches | Multiple | Spillmann, 1961 |
48 | Spawning release | Ova were scattered over the bed of the rivulet singly, in two and three and occassionaly in clumps of 4 together | No category | Kennedy and Fitzmaurice, 1972 |
48 | Spawning release | 1000 to 5000 eggs are released each time, and 8-15 days between each spawning and four spawning duraing the season | No category | Bruslé and Quignard, 2001 |
48 | Spawning release | Multiple spawner | Multiple | Rinchard, 1996 |
48 | Spawning release | Up to four batches | Multiple | Kestemont, 1987 |
48 | Spawning release | Released by small batches | Multiple | Billard, 1997 |
48 | Spawning release | Either single spawning per year of two to four spawnings per year | Total | Vila-Gispert and Moreno-Amich, 2002 |
48 | Spawning release | Typical multiple spawners | Multiple | Fredrich et al, 2003 |
48 | Spawning release | Most females lay two or more batches of eggs each season | Multiple | Mann, 1980 |
48 | Spawning release | Spawned repeatedly in four terms | No category | Penaz and Prokes, 1978 |
48 | Spawning release | Fractional | Fractional | Cattanéo et al, 2001 |
48 | Spawning release | Adopt multiple spawning strategies, with up to three batches of eggs produced by individual fish | Multiple | Nunn et al, 2007 |
48 | Spawning release | Ponte multiple | Multiple | Beelen et al, 1998/1999 |
48 | Spawning release | Pluralité de pontes d'une même femelle au cours d'une même saison | No category | Brunet and Hoestlandt, 1972 |
49 | Parity | Spawns once a year for several years | Iteroparous | Fishbase, 2006 |
49 | Parity | Both sex had low survival rates ad their reproductive life spans were rarely more than three years | No category | Mann, 1980 |
49 | Parity | Peut vivre de 5 à 7 années et se reproduire dès la seconde année | No category | Brunet and Hoestlandt, 1972 |
50 | Parental care | Nonguarder | No care | Fishbase, 2006 |
50 | Parental care | Non-guarder | No care | Mann, 1996 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |