Trait completeness | 80% |
Total data | 123 |
References | 16 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1 [Mean egg size] | 1.0 mm | Skryabin, 1993 |
1 | Oocyte diameter | About 1 | 1.0 mm | Spillmann, 1961 |
1 | Oocyte diameter | 0.9-1.4 | 1.15 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1 | 1.0 mm | Perrin, 2001 |
1 | Oocyte diameter | 0.9-1 | 0.95 mm | Fishbase, 2006 |
1 | Oocyte diameter | 0.9 [Not specffied] | 0.9 mm | Copp et al, 2002b |
1 | Oocyte diameter | 1.08 [Not specified] | 1.08 mm | Sauvonsaari, 1971 |
2 | Egg size after water-hardening | Mainly 1.1, varying between 0.8-1.15 [Drifting eggs] | 0.97 mm | Copp et al, 2002b |
2 | Egg size after water-hardening | Diameter of 1.0 mm and a tough outer skin | 1.0 mm | Smyly, 1955 |
3 | Egg Buoyancy | Demersal | Demersal | Kunz, 2004 |
3 | Egg Buoyancy | The eggs from these fish were found scattered over the bottom of the pond, the majority singly | Demersal | Smyly, 1955 |
4 | Egg adhesiveness | Adhesive, found attached to gravel and vegetation | Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive [stick to pebbles and gravels] | Adhesive | Losange, 1999 |
4 | Egg adhesiveness | Adhesive | Adhesive | Kunz, 2004 |
4 | Egg adhesiveness | Eggs adhere to the bottom and weeds | Adhesive | Sauvonsaari, 1971 |
5 | Incubation time | 14-16 [At 12-16°C] | 15.0 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 14-16 | 15.0 days | Bagenal, 1971 |
5 | Incubation time | Took 14-16 days at 12-16°C | 15.0 days | Smyly, 1955 |
5 | Incubation time | 16 days [14°C], 11 [18°C] and 7-8 [20°C] | 7.5 days | Sauvonsaari, 1971 |
6 | Temperature for incubation | 12-16 | 14.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | Took 14-16 days at 12-16°C | 15.0 °C | Smyly, 1955 |
6 | Temperature for incubation | 14-20°C | 17.0 °C | Sauvonsaari, 1971 |
7 | Degree-days for incubation | About 200 | 200.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | Took 14-16 days at 12-16°C | 15.0 °C * day | Smyly, 1955 |
7 | Degree-days for incubation | 16 days [14°C], 11 [18°C] and 7-8 [20°C] | 7.5 °C * day | Sauvonsaari, 1971 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 3-4 | 3.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | The newly hatched fry measured 3.0 mm in length | 3.0 mm | Smyly, 1955 |
13 | Full yolk-sac resorption | The yolk-sac is absorbed within 5-7 days [4.0-6.5 mm in size] | 6.0 °C * day | Smyly, 1955 |
13 | Full yolk-sac resorption | About 6 days | 6.0 °C * day | Bagenal, 1971 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1-2 | 1.5 year | Skryabin, 1993 |
15 | Age at sexual maturity | 1-2 | 1.5 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 2 | 2.0 year | Saat et al, 2003 |
15 | Age at sexual maturity | 2-3 [Mixed] | 2.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 2-3 [No specified] | 2.5 year | Environment agency, ??? |
15 | Age at sexual maturity | In Finland, the stone loach usually matures at the age of two years, those slower in development at the age of 3 years [Sex not specified] | 1.0 year | Sauvonsaari, 1971 |
16 | Length at sexual maturity | 7-7.3 | 7.15 cm | Skryabin, 1993 |
16 | Length at sexual maturity | 5.2-6.7 | 5.95 cm | Saat et al, 2003 |
16 | Length at sexual maturity | The smallest spawning female was 6.2 cm long | 6.2 cm | Sauvonsaari, 1971 |
17 | Weight at sexual maturity | 5.5-6 g | 5.75 kg | Skryabin, 1993 |
18 | Female sexual dimorphism | In many fish, the pectoral fin is relatively long and pointed in the male and round and short in the female. In most adult fish, but not all, the male pectoral fin was longer than that of the female; the distinction is therefore a useful but not infaillible means of determining sex from external examination. Immature fish could not be separate by this way. In the breeding season, no change of colour in either sex has been seen but small papillae, present on the pectoral fins of only male fish, have been found | Absent | Smyly, 1955 |
19 | Relative fecundity | 0.424 ± 0.019 [River Goloustnaya] and 0.552 ± 0.015 [River Olkha] | 0.42 thousand eggs/kg | Skryabin, 1993 |
19 | Relative fecundity | 0.216-0.833 | 0.52 thousand eggs/kg | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 1.710-27.600 in females of 70-182 mm, averaging 11.96 ± 0.72 | 11.96 thousand eggs | Skryabin, 1993 |
20 | Absolute fecundity | 1.7-27 | 14.35 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 500-800 eggs | 650.0 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | Total number of eggs varied between 5000 and 6000 of which usually rather then half were ripe | 5000.0 thousand eggs | Smyly, 1955 |
20 | Absolute fecundity | The number of eggs laid during one spawning period varies between 700 and 5000 | 700.0 thousand eggs | Sauvonsaari, 1971 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
22 | Onset of oogenesis | After autumn the GSI was 1.6 ± 0.24%, lower than that in the spring | ['April', 'May', 'June', 'October', 'November', 'December'] | Skryabin, 1993 |
22 | Onset of oogenesis | The GSI remained low during July and early August and increased thereafter | ['July', 'August'] | Saat et al, 2003 |
22 | Onset of oogenesis | Between September and February GSI lies between 5 and 10% | ['February', 'September'] | Smyly, 1955 |
23 | Intensifying oogenesis activity | The dynamics of GSI values and oocyte diameters in Estonia suggests that gonad reach stage IV (gonads with full-grown oocytes) already by late autumn (November) | ['October', 'November', 'December'] | Saat et al, 2003 |
23 | Intensifying oogenesis activity | The subsequent ripening of eggs and restoration of the GSI to April-May levels took 2.5-3 months | ['April', 'May'] | Skryabin, 1993 |
23 | Intensifying oogenesis activity | From March to June, with a few small fish excepted, this ratio lies on or above 10%, in a few instances reaching the high figures of 35% | ['March', 'April', 'May', 'June'] | Smyly, 1955 |
24 | Maximum GSI value | 30-32 [Before spawning in May] | 31.0 percent | Skryabin, 1993 |
24 | Maximum GSI value | 7.5-23.9 [November-December] and 16.3-24.6 [May] | 15.7 percent | Saat et al, 2003 |
24 | Maximum GSI value | From March to June, with a few small fish excepted, GSI lies on or above 10%, in a few instances reaching the high figures of 35%. From July to August, the ratio ranges between 3 and 20%, the higher values being largely late-spawners or non-spawners | 10.0 percent | Smyly, 1955 |
26 | Resting period | 1 [Short] | 1.0 months | Skryabin, 1993 |
26 | Resting period | 1 [Short] | 1.0 months | Saat et al, 2003 |
26 | Resting period | 2.8± 0.43 [After spawning in May] | 2.8 months | Skryabin, 1993 |
26 | Resting period | 2-8 [In July and beginning of August] | 5.0 months | Saat et al, 2003 |
26 | Resting period | From July to August, the GSI ranges between 3 and 20%, the higher values being largely late-spawners or non-spawners | 3.0 months | Smyly, 1955 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1 | 1.0 years | Skryabin, 1993 |
27 | Age at sexual maturity | 1 | 1.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2-3 [Male] | 2.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 2-3 [No specified] | 2.5 years | Environment agency, ??? |
28 | Length at sexual maturity | 5.1-6.6 | 5.85 cm | Saat et al, 2003 |
30 | Male sexual dimorphism | The second ray of pectoral fin is enlarged and longer, the second and eigth rays are recovered by sharp tubercules | Absent | Spillmann, 1961 |
30 | Male sexual dimorphism | The second ray is enlarged and longer and sharp tubercules on second and sixth rays of pectoral fin | Absent | Bruslé and Quignard, 2001 |
32 | Main spermatogenesis activity | August | ['August'] | Saat et al, 2003 |
33 | Maximum GSI value | 1.5-2 [Beginning of the spawning season] | 1.75 percent | Saat et al, 2003 |
33 | Maximum GSI value | The weight of testus was seldom more than 2% of the body weight | 2.0 percent | Smyly, 1955 |
35 | Resting period | 0.3-0.7 [Minimal value in mid-July, and by August GSI increased to about 1% and remained at this level until the next spring] | 6.0 months | Saat et al, 2003 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | The stone loach spawns in the same places where it lives | No data | Sauvonsaari, 1971 |
36 | Spawning migration distance | Limited home range | No data | Environment agency, ??? |
39 | Spawning season | April-June | ['April', 'June'] | Billard, 1997 |
39 | Spawning season | April-May | ['April', 'May'] | Spillmann, 1961 |
39 | Spawning season | April until June and sometimes July | ['April', 'May', 'June', 'July'] | Bruslé and Quignard, 2001 |
39 | Spawning season | Begin 10-12 May and end in the end of May | ['May'] | Skryabin, 1993 |
39 | Spawning season | Late April-Early August [England], May-June [Estonia], May and less June [Finland] | ['April', 'May', 'June', 'August'] | Saat et al, 2003 |
39 | Spawning season | April-June | ['April', 'June'] | Perrin, 2001 |
39 | Spawning season | Mainly April-May, also in March and June | ['March', 'April', 'May', 'June'] | Fishbase, 2006 |
39 | Spawning season | April-May | ['April', 'May'] | Losange, 1999 |
39 | Spawning season | April-May | ['April', 'May'] | Environment agency, ??? |
39 | Spawning season | Peak in 14 May | ['May'] | Bagenal, 1971 |
39 | Spawning season | In the Lake District, the fish spawns in May, though some breeding may take place in April and June, and a few ripe females have been found as late as July [Seasonal changes in the ratio gonad weight: body weight supports the conclusion that May is the month when most fish breed] | ['April', 'May', 'June', 'July'] | Smyly, 1955 |
39 | Spawning season | Spawning usually occurs in May, it may de delayed to early June in cold years | ['May', 'June'] | Sauvonsaari, 1971 |
40 | Spawning period duration | 12-14 [England], 4 [Estonia] and 4 [Finland] | 13.0 weeks | Saat et al, 2003 |
40 | Spawning period duration | 3-5 | 4.0 weeks | Skryabin, 1993 |
40 | Spawning period duration | Exact observations on the length of the spawning period are lacking andit may vary to some extend, depending on water temperature of the waer, but normally appears to take only a few days | No data | Sauvonsaari, 1971 |
41 | Spawning temperature | 6°C in the morning, 9-10°C | 9.5 °C | Skryabin, 1993 |
41 | Spawning temperature | Spawning begins as the shore waters warm to about 8°C | 8.0 °C | Sauvonsaari, 1971 |
42 | Spawning water type | Low productivity streams or high productivity environments | No category | Fishbase, 2006 |
42 | Spawning water type | Well oxygenated | Flowing or turbulent water | Losange, 1999 |
42 | Spawning water type | [In three successive years, fish in aquarium, in which the water was still, did not spawn; but a circular concrete ponds out of doors supplied with water from jets set at an angle so that the water in the pond was continually moving | Stagnant water | Smyly, 1955 |
43 | Spawning depth | Shallow waters | No data | Losange, 1999 |
43 | Spawning depth | Shore waters | No data | Sauvonsaari, 1971 |
44 | Spawning substrate | Psmanophile: gravels or roots of aquatic plants | Lithophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Gravels or aquatic plants | Lithophils | Spillmann, 1961 |
44 | Spawning substrate | Gravels and plants | Lithophils | Billard, 1997 |
44 | Spawning substrate | Gravel, aquatic plants | Lithophils | Perrin, 2001 |
44 | Spawning substrate | Lithophil | Lithophils | Kennedy, 1969 |
44 | Spawning substrate | Coarse gravel, stones | Lithophils | Environment agency, ??? |
44 | Spawning substrate | The eggs are not laid in holes but on stones and plants | Phytophils | Smyly, 1955 |
44 | Spawning substrate | Among shore rocks, eggs adhere to the bottom and weeds | Lithophils | Sauvonsaari, 1971 |
45 | Spawning site preparation | No | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Open water / substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | The eggs are not laid in holes but on stones and plants | No category | Smyly, 1955 |
46 | Nycthemeral period of oviposition | Night | Night | Skryabin, 1993 |
46 | Nycthemeral period of oviposition | It may be assumed with some certainty that spawning takes place in darkness either by night or on dark days | Day | Smyly, 1955 |
46 | Nycthemeral period of oviposition | Spawns at night | Night | Sauvonsaari, 1971 |
47 | Mating system | In the spawning act males and females come to lie on their sides belly to belly, so that reproductive openings are close together and fertilization is made more certain | No category | Smyly, 1955 |
48 | Spawning release | Two periods of spawning : May and late-summer-early autumn | Multiple | Skryabin, 1993 |
48 | Spawning release | One period of spawning | No category | Saat et al, 2003 |
48 | Spawning release | Multiple spawner | Multiple | Perrin, 2001 |
48 | Spawning release | Spawn only once a year for several years in low productivity streams, but exhibits multiple spawning within a season in high productivity environments | Multiple | Fishbase, 2006 |
48 | Spawning release | Interval of 2.5-3 months between first and second spawning event | No category | Skryabin, 1993 |
48 | Spawning release | About 4 [England], 2-3 [Estonia] and 1 [Finland] | No category | Saat et al, 2003 |
48 | Spawning release | Female lay their egg one by one | No category | Sauvonsaari, 1971 |
48 | Spawning release | Multiple spawning have been suggested | Multiple | Marconato and Rasotto, 1989 |
49 | Parity | Iteroparous | Iteroparous | Fishbase, 2006 |
49 | Parity | Specimens over four years old were rare, and only a few 6-year-olds were found | No category | Sauvonsaari, 1971 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |