Trait completeness | 80% |
Total data | 183 |
References | 40 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 8.29 ± 0.29 | 8.29 mm | Harzevili et al, 2004 |
8 | Initial larval size | 10 [Not specified if newly hatched] | 10.0 mm | Kestemont, 2001 |
8 | Initial larval size | 8.1 [3 days after hatching] | 8.1 mm | Wolnicki and Gorny, 1995 |
8 | Initial larval size | Total length of newly-hatched larvae is 5.5-8.7 mm (typically 7 mm). Larger larvae hatch from eggs incubated at higher temperatures, at 9°C : 6.6 (range 6.5-6.8) mm; at 13.4°C : 7.3 (range 6.3-7.5) mm; at 22°C : 7.4 (6.5-8.4) mm. Newly hatched larvae of ide are mode developmentally advanced compared to larvae of other cyprinid fishes | 7.1 mm | Witkowski et al, 1997 |
8 | Initial larval size | 7.3 ± 0.4 [Not specified if at hatching] | 7.3 mm | Wolnicki et al, ??? |
9 | Larvae behaviour | Larvae have well developped cement glands with which they fix themselves to plants where their development occurs. Active swiimming in horizontal position begins 4 days after hatching. At that time their swim bladder is being filled with air | Demersal | Witkowski et al, 1997 |
10 | Reaction to light | Larvae are intially photophobic | Photophobic | Mann, 1996 |
10 | Reaction to light | Larve are not photophobic | Photopositive | Witkowski et al, 1997 |
11 | Temperature during larval development | 19-20 | 19.5 °C | Harzevili et al, 2004 |
11 | Temperature during larval development | Reared at 25°C | 25.0 °C | Wolnicki and Gorny, 1995 |
11 | Temperature during larval development | Reared at 20-25 | 22.5 °C | Kamler and Wolnicki, 2006 |
11 | Temperature during larval development | Optimal temperature for larval development is about 17°C. Lethal temperatures are 23.7-29.1°C for ide larvae and juveniles. | 26.4 °C | Witkowski et al, 1997 |
11 | Temperature during larval development | Optimum temperatures for larval growth (expressed as Relative growth rate: RGR, %d): 19-25°C or 26-31°C | 22.0 °C | Wolnicki, 2005 |
11 | Temperature during larval development | Reared at 25, 28 and 31 | 25.0 °C | Wolnicki et al, ??? |
11 | Temperature during larval development | Can be realized at 24-26°C | 25.0 °C | Kestemont and Mélard, 1994 |
11 | Temperature during larval development | Water was maintained at 24.0 ± 0.5°C | 24.0 °C | Hamackova et al, 2007 |
13 | Full yolk-sac resorption | The resorption of the yolk-sac lasts about 80-90 DD | 85.0 °C * day | Kestemont and Mélard, 1994 |
13 | Full yolk-sac resorption | Other studies stated that, for ide, at 25°C water temperature, 50% of starving fry were killed after 9 days of nursing, and 95% after 10 days. In our case, total kill of starving fry occurred during the 10th day of nursing | 25.0 °C * day | Hamackova et al, 2007 |
14 | Onset of exogeneous feeding | 70-90 [4-5 days at 19-20°C] | 80.0 °C * day | Harzevili et al, 2004 |
14 | Onset of exogeneous feeding | Beginning from day 3 after hatching the larvae (TL=8.1 at 25°C] were supplied exclusively with freshly hatched Artemia salina nauplii or exclusively commercial dry feed or both] | 3.0 °C * day | Wolnicki and Gorny, 1995 |
9 | Larvae behaviour | benthic | Demersal | Witaska et al, 2014 |
9 | Larvae behaviour | Pelagic | Pelagic | Witaska et al, 2014 |
10 | Reaction to light | photopositive | Photopositive | Kupren et al, 2015 |
8 | Initial larval size | 7.74 | 7.74 mm | Kupren et al, 2015 |
8 | Initial larval size | 7.39-8.08 | 7.73 mm | Kupren et al, 2015 |
9 | Larvae behaviour | Pelagic | Pelagic | Kupren et al, 2015 |
8 | Initial larval size | 6.18-7.13 | 6.65 mm | Krupen et al, 2011 |
14 | Onset of exogeneous feeding | 6.1-12 days | 9.05 °C * day | Krupen et al, 2011 |
11 | Temperature during larval development | 23 | 23.0 °C | Krupen et al, 2011 |
13 | Full yolk-sac resorption | 7.5-13.2 days 15.7 C | 10.35 °C * day | Krupen et al, 2011 |
14 | Onset of exogeneous feeding | 6.1-12 days 15.7 C | 9.05 °C * day | Krupen et al, 2011 |
8 | Initial larval size | 5 | 5.0 mm | Pinder, 2001 |
11 | Temperature during larval development | 10-14 | 12.0 °C | Krejszeff et al, 2009 |
14 | Onset of exogeneous feeding | 23.7 days 12.3 C | 23.7 °C * day | Kupren et al, 2008 |
14 | Onset of exogeneous feeding | 21.3 days 12.3 C | 21.3 °C * day | Kupren et al, 2008 |
14 | Onset of exogeneous feeding | 6.8 days 23.0 C | 6.8 °C * day | Kupren et al, 2008 |
14 | Onset of exogeneous feeding | 6.1 days 23.0 C | 6.1 °C * day | Kupren et al, 2008 |
13 | Full yolk-sac resorption | 24 days 12.3 C | 24.0 °C * day | Kupren et al, 2008 |
13 | Full yolk-sac resorption | 7.5 days 23.0 C | 7.5 °C * day | Kupren et al, 2008 |
8 | Initial larval size | 6.37 at 7.42 | 6.37 mm | Kupren et al, 2010 |
9 | Larvae behaviour | pelagic | Pelagic | Kupren et al, 2015 |
11 | Temperature during larval development | 9.5-23 | 16.25 °C | Kupren et al, 2008 |
11 | Temperature during larval development | 12.3-25 | 18.65 °C | Kupren et al, 2010 |
13 | Full yolk-sac resorption | 4.0 | 4.0 °C * day | Kupren et al, 2015 |
14 | Onset of exogeneous feeding | 9.5 | 9.5 °C * day | Kupren et al, 2008 |
14 | Onset of exogeneous feeding | 2.0 | 2.0 °C * day | Kupren et al, 2015 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2-5 [Sex no specified] | 3.5 year | Kestemont, 2001 |
15 | Age at sexual maturity | 5-6 [Female] | 5.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | In southern and central Europe, first spawning-ide are age 3-5 years, sometimes they are 2 years old. In eastern Europe, reproductive period begins at the age of 4 and 5 years. More precisely 6 years [Kävlingean], 5 years [Dniepr], (3) 4 [Dunaj] | 4.0 year | Witkowski et al, 1997 |
15 | Age at sexual maturity | Between 2-5 years [Sex not specified] | 3.5 year | Kestemont and Mélard, 1994 |
16 | Length at sexual maturity | 41-49 [Unsexed] | 45.0 cm | Fishbase, 2006 |
16 | Length at sexual maturity | Standard length of females reaches 170-330 mm. More precisely 315-328 [Kävlingean], 190 [Dniepr], 281-306 [Dunaj] for females | 250.0 cm | Witkowski et al, 1997 |
17 | Weight at sexual maturity | 0.4 [Sex no specified] | 0.4 kg | Kestemont, 2001 |
17 | Weight at sexual maturity | 523-760 g [In Sarvlax], 200-300 [In Dunaj], sex not specified | 641.5 kg | Witkowski et al, 1997 |
19 | Relative fecundity | 120-160 | 140.0 thousand eggs/kg | Kestemont, 2001 |
19 | Relative fecundity | 84 eggs per g of body weight of female | 84.0 thousand eggs/kg | Witkowski et al, 1997 |
19 | Relative fecundity | About 100 000 eggsper kg of female | 100.0 thousand eggs/kg | Kestemont and Mélard, 1994 |
20 | Absolute fecundity | About 100 | 100.0 thousand eggs | Spillmann, 1961 |
20 | Absolute fecundity | 60 [For female of 0.5 kg] to 160 [For female of 0.5-2 kg] | 1.25 thousand eggs | Kestemont, 2001 |
20 | Absolute fecundity | Ranges from 8731-263412, mean about 45000 to 88000 | 136071.5 thousand eggs | Witkowski et al, 1997 |
20 | Absolute fecundity | A female can spawn about 100 000 eggs | 100.0 thousand eggs | Kestemont and Mélard, 1994 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
22 | Onset of oogenesis | Maturation of gonads is synchrnous and complete in the previous autumn | ['October', 'November', 'December'] | Fredrich et al, 2003 |
22 | Onset of oogenesis | Ovaries start developing in June | ['June'] | Witkowski et al, 1997 |
22 | Onset of oogenesis | Data collected in the orfe and nase show that the transition of oocytes in the stage of primary growth into the stage of cortical alveoli takes place in July-August and vitellogenesis already starts in August-September | ['July', 'August', 'September'] | Lefler et al, 2008 |
23 | Intensifying oogenesis activity | 13.12 ± 2.41 [In October] to 19.14 ± 2.24 [In April] | ['April', 'October'] | Lefler et al, 2006 |
24 | Maximum GSI value | GSI of mature females just before spawning (March-April) ranges from 7 to 20%, typically about 12%. In Scandinavian populations GSI value are higher, from 17 to 30% (mean 21%) | 7.0 percent | Witkowski et al, 1997 |
24 | Maximum GSI value | 19.14 ± 2.24 [In April] | 19.14 percent | Lefler et al, 2006 |
24 | Maximum GSI value | GSI =18.57 % in March 29 (n=5) | 18.57 percent | Lefler et al, 2008 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2-5 [Sex no specified] | 3.5 years | Kestemont, 2001 |
27 | Age at sexual maturity | 5 [Male] | 5.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | As a rule, male mature one year earlier than females. In southern and central Europe, first spawning-ide are age 3-5 years, sometimes they are 2 years old. In eastern Europe, reproductive period begins at the age of 4 and 5 years. More precisely 6 years [Kävlingean], 4 years [Dniepr], (3) 4 [Dunaj] | 4.0 years | Witkowski et al, 1997 |
28 | Length at sexual maturity | 41-49 [Unsexed] | 45.0 cm | Fishbase, 2006 |
28 | Length at sexual maturity | Standard length of males reaches 180-310 mm. More precisely 220 [Dniepr], 278-310 [Dunaj] for males | 245.0 cm | Witkowski et al, 1997 |
29 | Weight at sexual maturity | 0.4 [Sex no specified] | 0.4 kg | Kestemont, 2001 |
29 | Weight at sexual maturity | 523-760 g [In Sarvlax], 200-300 [In Dunaj], sex not specified | 641.5 kg | Witkowski et al, 1997 |
30 | Male sexual dimorphism | Yellowish or white breeding tubercles apear in males during the spawning on the anterior part of the head | Absent | Witkowski et al, 1997 |
32 | Main spermatogenesis activity | In November, the colour of testes changes from red to whitish, which is indicative of the presence of spermatozoans | ['November'] | Witkowski et al, 1997 |
33 | Maximum GSI value | In March-April, the mass of testes accounts for only 1.8% of body weight | 1.8 percent | Witkowski et al, 1997 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Maximally 2.5 km | 2.5 km | Witkowski et al, 1997 |
36 | Spawning migration distance | Potamodromous with a prevailing upstream migration | No data | Kuliskova et al, 2009 |
37 | Spawning migration period | Leave their winter shelters from the main channel of danube for entering into the spawning areas when water temperature is about 4-6°C | ['January', 'February', 'March'] | Ciolac, 2004 |
37 | Spawning migration period | In early spring (beginning of April) ide migrate upstream to spawning grounds. Populations linving in brackish Baltic waters migrate in May-June to spawn in rivers or near-shore lakes | ['April', 'May', 'June'] | Witkowski et al, 1997 |
38 | Homing | It was observed that individuals spawn on the same places as in previous years. Thus, homing was reported for ide, similarly as for salmonid (and same other) fish | Present | Witkowski et al, 1997 |
38 | Homing | Displaying a homing behaviour | Present | Kuliskova et al, 2009 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Billard, 1997 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Spillmann, 1961 |
39 | Spawning season | March-April | ['March', 'April'] | Kestemont, 2001 |
39 | Spawning season | May [From March to June] | ['March', 'April', 'May', 'June'] | Fishbase, 2006 |
39 | Spawning season | April-May | ['April', 'May'] | Mann, 1996 |
39 | Spawning season | Late winter or early spring | ['January', 'February', 'March', 'April', 'May', 'June'] | Fredrich et al, 2003 |
39 | Spawning season | April-May | ['April', 'May'] | Kamler and Wolnicki, 2006 |
39 | Spawning season | In southern and central Europe ide begin spawning in the second half of March or at the beginning of April. In nothern Europe and Siberia, spawning begins later - in the middle of May, or in June | ['March', 'April', 'May', 'June'] | Witkowski et al, 1997 |
39 | Spawning season | March-April | ['March', 'April'] | Kestemont and Mélard, 1994 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Kuliskova et al, 2009 |
40 | Spawning period duration | Several days [Male arrives first on spawning grounds] | No data | Billard, 1997 |
40 | Spawning period duration | Spanwing is short , 2-5 days at 8-12°C. At lower temperatures may last two weeks, during cold springs spawning duration may be prolonged to> one month | 3.5 weeks | Witkowski et al, 1997 |
41 | Spawning temperature | 4-15, but rarely above 12-13°C | 9.5 °C | Kestemont, 2001 |
41 | Spawning temperature | 4-15 | 9.5 °C | Mann, 1996 |
41 | Spawning temperature | 6-10 | 8.0 °C | Kamler and Wolnicki, 2006 |
41 | Spawning temperature | Spawning begins when water temperature increases up to 5.5°C. During spawning mean temperatures of water are 6-10°C, extreme temperatures are 3 and 15°C. | 8.0 °C | Witkowski et al, 1997 |
41 | Spawning temperature | When temperature reaches 13°C | 13.0 °C | Kestemont and Mélard, 1994 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Billard, 1997 |
42 | Spawning water type | Ide spawn in rivers, streams, old arms, lakes, dam reservoirs, and meadows covered with flood waters. | Stagnant water | Witkowski et al, 1997 |
43 | Spawning depth | Shallow waters | No data | Billard, 1997 |
43 | Spawning depth | Shallow waters | No data | Fishbase, 2006 |
44 | Spawning substrate | Plants or sandy grounds | Phytophils | Spillmann, 1961 |
44 | Spawning substrate | Plants or gravels | Lithophils | Billard, 1997 |
44 | Spawning substrate | Stones, sand or with plants | Phytophils | Kestemont, 2001 |
44 | Spawning substrate | Gravel, weed, stones | Lithophils | Fishbase, 2006 |
44 | Spawning substrate | Eggs adhere to submerged plants, but other substrata are utilised if suitable plants are absent, pebbles | Phytophils | Mann, 1996 |
44 | Spawning substrate | Phytolithophil | Lithophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Eggs are deposited on submerged plants, as well as roots, trunks, and branches of fallen trees, but they can be laid on stones, gravel, sand, and a muddy bottom. Thus classified as an indifferent lithophytophilous | Phytophils | Witkowski et al, 1997 |
44 | Spawning substrate | Plants or sandy bottoms | Phytophils | Kestemont and Mélard, 1994 |
44 | Spawning substrate | Phytolithophic | No category | Kuliskova et al, 2009 |
45 | Spawning site preparation | Open water/substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawners | Open water/substratum scatter | Mann, 1996 |
48 | Spawning release | Multiple | Multiple | Rinchard, 1996 |
48 | Spawning release | Once a year | Total | Kestemont, 2001 |
48 | Spawning release | Spawn once a year | Total | Fredrich et al, 2003 |
48 | Spawning release | Single spawner | Total | Lefler et al, 2006 |
48 | Spawning release | Single spawner | Total | Lefler et al, 2008 |
49 | Parity | Live up to 10-15, even 20 years of age | No category | Bruslé and Quignard, 2001 |
49 | Parity | Maximum life span of ide is 18 years, maximum length (TL) 70 cm, maximum weight 6-8 kg | No category | Witkowski et al, 1997 |
49 | Parity | Can reach 15 years | No category | Kestemont and Mélard, 1994 |
49 | Parity | In contrast, L. idus was observed to undertake similar long-distance migrations in spring but in the opposite direction, i.e. downstream during spring and returning upstream towards formely occupied areas later in the season | No category | Kuliskova et al, 2009 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |