Trait completeness | 84% |
Total data | 199 |
References | 25 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 0.34-1.3 (first batch : 0.90-1.21 and second batch 0.36-0.47) | 0.82 mm | Ogle, 1998 |
1 | Oocyte diameter | 1 | 1.0 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 0.34-1.33 [Eggs from first batch are larger 0.90-1.21, and second batch are smaller 0.36-0.47 mm] | 0.41 mm | Crosier et al, 2005 |
1 | Oocyte diameter | 1 | 1.0 mm | Spillmann, 1961 |
1 | Oocyte diameter | Average is 1 | 1.0 mm | Craig, 2000 |
1 | Oocyte diameter | 0.9-1.2 | 1.05 mm | Crivelli and Rosecchi, 2001 |
1 | Oocyte diameter | 0.5-1 | 0.75 mm | Fishbase, 2006 |
1 | Oocyte diameter | 0.86-1.0 [End of hydratation process, unfertilized egg] | 0.93 mm | Bonislawska et al, 2004 |
1 | Oocyte diameter | The maximum diameter reaching 0.98 (in ova). Other described as 1.03 (range0.90-1.21) | 1.05 mm | Neja, 1988 |
1 | Oocyte diameter | Immediatly before spawning the maturing oocyte diameters varied between 0.650 and 0.850 mm | 0.85 mm | Luksiene et al, 2000 |
2 | Egg size after water-hardening | 0.97-1.07 [Activated egg] | 1.02 mm | Kovac, 1998 |
2 | Egg size after water-hardening | The egg diameter was measured in the middle of the spawning season: 0.65-0.85 [In lake Peipsi], 0.9-1.1 [In Matsalu Bay], 0.95-1.25 |In Pärnu Bay] | 0.75 mm | Albert et al, 2006 |
3 | Egg Buoyancy | Demersal | Demersal | Bruslé and Quignard, 2001 |
3 | Egg Buoyancy | On the bottom demersal | Demersal | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive, sticking to stones or submerged vegetation | Adhesive | Craig, 2000 |
4 | Egg adhesiveness | Upon contact with water, eggs become adhesive and will attach to various substrates | Adhesive | Crosier et al, 2005 |
4 | Egg adhesiveness | Ruffle eggs become adhesive upon contact with water and stick to substrate | Adhesive | Ogle, 1998 |
4 | Egg adhesiveness | Sticky | Adhesive | Spillmann, 1961 |
4 | Egg adhesiveness | Very adhesive | Adhesive | Kovac, 1998 |
4 | Egg adhesiveness | Sticky, in a gelly matrix | Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
5 | Incubation time | 5-12 [At 10-15°C] | 8.5 days | Ogle, 1998 |
5 | Incubation time | 5-12 [At 10-15°C] | 8.5 days | Crosier et al, 2005 |
5 | Incubation time | About 10 | 10.0 days | Spillmann, 1961 |
5 | Incubation time | 8-10 [at 10-15°C] | 9.0 days | Craig, 2000 |
5 | Incubation time | [First hatching at 123 hours and 50% left the egg shells 4 hour later, the last larvae hatched within additional 5 hour in their experiment, others give: from 4.5 at 15-16°C to 27-29 at 6°C] | 15.5 days | Bonislawska et al, 2004 |
5 | Incubation time | 8-12 | 10.0 days | Maitland, 1977 |
5 | Incubation time | 5-6 [At 16°C] | 5.5 days | Brown et al, 1998 |
6 | Temperature for incubation | 15 is the optima temperature for "early development" [Lower TL50 = 10; Upper TL50 = 21.5] | 15.0 °C | Ogle, 1998 |
6 | Temperature for incubation | 12-13 | 12.5 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | 10-15 | 12.5 °C | Crosier et al, 2005 |
6 | Temperature for incubation | Optimal 15, range 9-21 | 15.0 °C | Saat and Veersalu, 1996 |
6 | Temperature for incubation | Optimal range is 16-18°C [Temperature tested in other studies from 6 to 22°C] | 17.0 °C | Bonislawska et al, 2004 |
6 | Temperature for incubation | 16°C | 16.0 °C | Brown et al, 1998 |
6 | Temperature for incubation | Two incubation temperature at 12 ±0.2°C and 14 ± 2°C | 12.0 °C | Vetemaa and Saat, 1996 |
6 | Temperature for incubation | The dishes were kept under the same conditions under natural photoperiod at 16°C | 16.0 °C | Albert et al, 2006 |
7 | Degree-days for incubation | 130-150 | 140.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 100-120 [5-12 at 10-15°C] | 110.0 °C * day | Crosier et al, 2005 |
7 | Degree-days for incubation | 100-120 [8-10 at 10-15°C] | 110.0 °C * day | Craig, 2000 |
7 | Degree-days for incubation | About 90 [5-6 days at 16°C] | 5.5 °C * day | Brown et al, 1998 |
7 | Degree-days for incubation | 136 | 136.0 °C * day | Kovac, 1998 |
7 | Degree-days for incubation | [From 1962 to 2032 degree hour, 50% at 2032, others give 67.5 to 174] | 1962.0 °C * day | Bonislawska et al, 2004 |
1 | Oocyte diameter | 0.90-1.20 | 1.05 mm | French and Edsall, 1992 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 3.5-4.4 | 3.95 mm | Ogle, 1998 |
8 | Initial larval size | 3 | 3.0 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 3.5-4.4 | 3.95 mm | Crosier et al, 2005 |
8 | Initial larval size | 3 | 3.0 mm | Spillmann, 1961 |
8 | Initial larval size | 2.5-3.2 | 2.85 mm | Craig, 2000 |
8 | Initial larval size | 3.35-3.81 | 3.58 mm | Kovac, 1998 |
8 | Initial larval size | 3.85 ± 0.08 [Other give 3.52 to 4.29] | 3.85 mm | Bonislawska et al, 2004 |
8 | Initial larval size | Standard length of larvae of freswater : meanSL range from 2.05 and 2.23 and brackishwater range from 2.32-3.03 | 2.67 mm | Albert et al, 2006 |
9 | Larvae behaviour | Embryo remains sedentary on the bottom for 3 to 7 days until reaching a size of 4.5-5.0 | Demersal | Ogle, 1998 |
9 | Larvae behaviour | Remain sedentary for 3-7 days | Demersal | Crosier et al, 2005 |
9 | Larvae behaviour | Most to the time they stay at the bottom | Demersal | Kovac, 1998 |
9 | Larvae behaviour | Immediate dispersion after hatching | Demersal | Urho, 2002 |
9 | Larvae behaviour | The larvae easily stayed in the water column and were fully prepapred for independent living in external environment | Demersal | Bonislawska et al, 2004 |
9 | Larvae behaviour | Larval ruffe hatch and become pelagic within 1 to 2 weeks after egg deposition and could possibly be netrained in ballast water duting the pelagic period | Pelagic | Brown et al, 1998 |
10 | Reaction to light | Positively phototactic, little or no pelagic stage | Photopositive | Ogle, 1998 |
10 | Reaction to light | Larvae are intially photophobic | Photophobic | Mann, 1996 |
11 | Temperature during larval development | 25-30 optimal temperature for larval growth, larval survival is poor below 10°C [Possibly between 7.0°C to 24.8°C] | 27.5 °C | Ogle, 1998 |
11 | Temperature during larval development | 25-30 optimal temperature for larval growth | 27.5 °C | Craig, 2000 |
11 | Temperature during larval development | At water temperature ranging from 16.2 to 23.2°C (mean 19.4°C), the larval period lasted 20 days | 16.2 °C | Kovac, 1998 |
11 | Temperature during larval development | Larvae were captured at Allouez Bay from 30 May to 10 July, with peak catch the week of 13 June, corresponds to a temperature of 12-17°C on the graph. Larvae were captured at whaleback from 23 May to 3 June with a peak catch the week of 30 May, which corresponds to 12-16°c on the graph | 14.5 °C | Brown et al, 1998 |
13 | Full yolk-sac resorption | Active feeding and swimming occur within one week of hatching after the yolk-sac is absorbed | No data | Crosier et al, 2005 |
14 | Onset of exogeneous feeding | Feeding begins after about 1 week | 1.0 °C * day | Crosier et al, 2005 |
14 | Onset of exogeneous feeding | The transition to exogenous feeding takes plance in benthopelagic layer about 1 week after hatching | 1.0 °C * day | Ogle, 1998 |
14 | Onset of exogeneous feeding | 120-130: Active feeding and swim-up occurring 13 days after fertilization (hatching 5-6 days after fertilization) at 16°C | 125.0 °C * day | Brown et al, 1998 |
8 | Initial larval size | 2.50-3.20 | 2.85 mm | French and Edsall, 1992 |
13 | Full yolk-sac resorption | 7 days @ 20-22 C | 21.0 °C * day | French and Edsall, 1992 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2-3 but sometimes 1 [Sex not specified] | 2.5 year | Ogle, 1998 |
15 | Age at sexual maturity | 2 [Sex not specified] | 2.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 2 [Part of the population at 1] | 2.0 year | Kovac, 1998 |
15 | Age at sexual maturity | 1-3 [Sex not specified] | 2.0 year | Crivelli and Rosecchi, 2001 |
15 | Age at sexual maturity | 1-2 | 1.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 2 [Not specified] | 2.0 year | Environment agency, ??? |
15 | Age at sexual maturity | 2-3 [Not specified] | 2.5 year | Maitland, 1977 |
15 | Age at sexual maturity | All the individuals caught before spawning and belonging to age group 2 and older groups had their gonads at stage 4 or 5, that is they were ready to the nearest spawning. One may infer that some individuals spawn as early as at age 1+. In Poland, it marres at the end of its second year of life. In the river Nadym drainage, it matures at age 2 (usually hower, 3+ or 4+) | 2.0 year | Neja, 1988 |
16 | Length at sexual maturity | 11-12 [Sex not specified] | 11.5 cm | Ogle, 1998 |
16 | Length at sexual maturity | 11-12 [Sex not specified] but sometimes 6.5-7.0 | 11.5 cm | Craig, 2000 |
16 | Length at sexual maturity | 5.7-9 SL [All female exceeding 9 cm were mature] | 7.35 cm | Kovac, 1998 |
16 | Length at sexual maturity | Described as 11-12, but also at 6.5-7.0 [sex not specified] | 11.5 cm | Neja, 1988 |
17 | Weight at sexual maturity | 20-30 g ! [Different class studied strating at 11.0-20.9 g !] | 25.0 kg | Neja, 1988 |
19 | Relative fecundity | 352-1540 | 946.0 thousand eggs/kg | Ogle, 1998 |
19 | Relative fecundity | 585-1540 | 1062.5 thousand eggs/kg | Kovac, 1998 |
19 | Relative fecundity | 305-1540 | 922.5 thousand eggs/kg | Crivelli and Rosecchi, 2001 |
19 | Relative fecundity | Mean 1066.3, range 585-1540 eggs/g | 1062.5 thousand eggs/kg | Neja, 1988 |
20 | Absolute fecundity | 10-150 | 80.0 thousand eggs | Crosier et al, 2005 |
20 | Absolute fecundity | 4-200 for the first batch and 0.352-6 for the second | 102.0 thousand eggs | Ogle, 1998 |
20 | Absolute fecundity | 40-1000 | 520.0 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 100-150 | 125.0 thousand eggs | Spillmann, 1961 |
20 | Absolute fecundity | 17.8 is the average [13-82] | 47.5 thousand eggs | Craig, 2000 |
20 | Absolute fecundity | 4-100 | 52.0 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | 4-105 | 54.5 thousand eggs | Maitland, 1977 |
20 | Absolute fecundity | 13.338-82.233 | 47.79 thousand eggs | Neja, 1988 |
21 | Oocyte development | Group- synchronous, multiple clutches [ovaries may contain several oocytes stages simultaneously] | Synchronous | Leino and McCormick, 1997 |
21 | Oocyte development | Polycyclic, with asynchrous ripening of eggs and protracted spawning | Asynchronous | Kovac, 1998 |
21 | Oocyte development | A mature ruffe ovary contains three types of eggs: 1) small, hyaline, and clorless; 2) larger, opaque, white and orange in color; and 3) large, partly hyaline, and yellow-orange and ornage in color. Only the latter two types will be released during the next spawing season | No category | Ogle, 1998 |
21 | Oocyte development | Asynchronous development | Asynchronous | Luksiene et al, 2000 |
22 | Onset of oogenesis | Oocytes mature in 165 days in winter and 30 days during summer | ['January', 'February', 'March', 'July', 'August', 'September'] | Ogle, 1998 |
22 | Onset of oogenesis | Between September and March, gonad weight increases slowly | ['March', 'September'] | Kovac, 1998 |
22 | Onset of oogenesis | September slight increase | ['September'] | Leino and McCormick, 1997 |
22 | Onset of oogenesis | In September, most females (64.1%) had ovaries at stage 2. No stage 4 gonads were found at that time | ['September'] | Neja, 1988 |
23 | Intensifying oogenesis activity | March-April | ['March', 'April'] | Leino and McCormick, 1997 |
24 | Maximum GSI value | 7.1-15.6 [Average spawning GSI] | 11.35 percent | Ogle, 1998 |
24 | Maximum GSI value | 9-11 [May] | 10.0 percent | Brown et al, 1998 |
24 | Maximum GSI value | 8-11 [April] | 9.5 percent | Leino and McCormick, 1997 |
24 | Maximum GSI value | Gonad in stage VI, meaN: 13.81, range 9.52-24.29 [In other study, the coefficient in females migrating to spawn to average 15.6 (9.0-22.0)] | 16.91 percent | Neja, 1988 |
26 | Resting period | 2-3 [June, July and August] | 2.5 months | Leino and McCormick, 1997 |
26 | Resting period | <1 | 1.0 months | Leino and McCormick, 1997 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2-3 but sometimes 1 [Sex not specified] | 2.5 years | Ogle, 1998 |
27 | Age at sexual maturity | 2 [ sex not specified] | 2.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2 [Part of the population at 1] | 2.0 years | Kovac, 1998 |
27 | Age at sexual maturity | 1-3 [Sex not specified] | 2.0 years | Crivelli and Rosecchi, 2001 |
27 | Age at sexual maturity | 1 [Male] | 1.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | 2 [Not specified] | 2.0 years | Environment agency, ??? |
28 | Length at sexual maturity | 11-12 [Sex not specified] | 11.5 cm | Ogle, 1998 |
28 | Length at sexual maturity | 11-12 [Sex not specified] but sometimes 65-70 | 11.5 cm | Craig, 2000 |
28 | Length at sexual maturity | 3.2-8 SL [All male exceeding 8 cm were mature] | 5.6 cm | Kovac, 1998 |
31 | Onset of spermatogenesis | Male gonadal activity occurs during spring and autumn | ['April', 'May', 'June', 'October', 'November', 'December'] | Crosier et al, 2005 |
31 | Onset of spermatogenesis | Two periods of gonad activity are observed in males in the course of the year; spring and autumn wves of spermatogenesis occur [Winter conditions provoke a considerable slowing down of spermatogenesis, ending in most specimens (81%) with its cessation in the phase of reprodcution of spermatogonia | ['January', 'February', 'March', 'April', 'May', 'June', 'October', 'November', 'December'] | Butskaya, 1981 |
31 | Onset of spermatogenesis | In September, male gonads were more advanced in development (23.5% and 76.5% at stage 2 and 3, respectively). No stage 4 gonads were found at that time | ['September'] | Neja, 1988 |
32 | Main spermatogenesis activity | The peak of the spring wave of spermatogenesis, is observed annually under natural conditions, in late May, when all phases of spermatogenesis, from the reprodcution of spermatogonia to the formationof new ripe spermatozoids, are found in cysts of the testes. | ['April', 'May', 'June'] | Butskaya, 1981 |
33 | Maximum GSI value | 7-10 [Average spawning male GSI] | 8.5 percent | Ogle, 1998 |
33 | Maximum GSI value | In 3 test fish, the coefficient of maturity was 3.74, 4.18 and 4.80 | 3.0 percent | Butskaya, 1981 |
33 | Maximum GSI value | Male in VI stage, were on average 7.11, range 5.26-12.18 | 8.72 percent | Neja, 1988 |
35 | Resting period | Periods in which gametogensis is absent occuring between spring and autumn [The coefficients of maturity after discharge of the spermatozoids (in the absence of spermatogensis) is on average 0.8% (range 0.5-1.2%), and after completion of the rearrangement of the somatic elements of the testes less than 0.25% | 7.0 months | Butskaya, 1981 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Ruffe do not make long migrations, however short diurnal and seasonal movements are common | No data | Kovac, 1998 |
36 | Spawning migration distance | Limited home range | No data | Environment agency, ??? |
37 | Spawning migration period | Undergoes spawning migrations from winter habitats which are deep areas in river or lakes to shallow areas which are stony and covered with aquatic macrophytes | ['January', 'February', 'March'] | Craig, 2000 |
39 | Spawning season | March to May | ['March', 'April', 'May'] | Spillmann, 1961 |
39 | Spawning season | May-July | ['May', 'July'] | Brown et al, 1998 |
39 | Spawning season | April-May but June in Nothern Region | ['April', 'May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | Usually during April-July | ['April', 'July'] | Crosier et al, 2005 |
39 | Spawning season | Mid-April to July | ['April', 'May', 'June', 'July'] | Ogle, 1998 |
39 | Spawning season | April-June | ['April', 'June'] | Craig, 2000 |
39 | Spawning season | Mid-April to Mid-June | ['April', 'May', 'June'] | Kovac, 1998 |
39 | Spawning season | Late April to Mid-June | ['April', 'May', 'June'] | Leino and McCormick, 1997 |
39 | Spawning season | March to May | ['March', 'April', 'May'] | Billard, 1997 |
39 | Spawning season | March to August | ['March', 'April', 'May', 'June', 'July', 'August'] | Crivelli and Rosecchi, 2001 |
39 | Spawning season | April-May but also March to up to August | ['March', 'April', 'May', 'August'] | Fishbase, 2006 |
39 | Spawning season | March-July | ['March', 'July'] | Mann, 1996 |
39 | Spawning season | March-May | ['March', 'May'] | Environment agency, ??? |
39 | Spawning season | March to early May | ['March', 'May'] | Terver, 1984 |
39 | Spawning season | April-May | ['April', 'May'] | Maitland, 1977 |
39 | Spawning season | In Polish waters typically from mid-April through end of May | ['April', 'May'] | Neja, 1988 |
40 | Spawning period duration | 8 | 8.0 weeks | Brown et al, 1998 |
40 | Spawning period duration | 8 | 8.0 weeks | Leino and McCormick, 1997 |
40 | Spawning period duration | 7-8 | 7.5 weeks | Terver, 1984 |
40 | Spawning period duration | Started spawning in early May, the spawning lasting no longer than until early June | No data | Neja, 1988 |
41 | Spawning temperature | 6-18 | 12.0 °C | Ogle, 1998 |
41 | Spawning temperature | 5-18 [mainly between 12-14] | 11.5 °C | Brown et al, 1998 |
41 | Spawning temperature | 10-15 | 12.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | Spawning begins when temperature reach 6°C | 6.0 °C | Crosier et al, 2005 |
41 | Spawning temperature | 11.6-18.0 is the normal range but could start at 6-8 | 14.8 °C | Craig, 2000 |
41 | Spawning temperature | 7.1-20.2 | 13.65 °C | Kovac, 1998 |
41 | Spawning temperature | 12-18 | 15.0 °C | Crivelli and Rosecchi, 2001 |
41 | Spawning temperature | 11.6-18 | 14.8 °C | Saat and Veersalu, 1996 |
41 | Spawning temperature | 6-12 | 9.0 °C | Mann, 1996 |
42 | Spawning water type | Where the current is fairly rapid | Flowing or turbulent water | Craig, 2000 |
42 | Spawning water type | Spawning of Eurasian ruffe in the the Baka side-arm system of the River Danube, in the Orava Reservoir, Lipno reservoir | No category | Kovac, 1998 |
43 | Spawning depth | Shallow water with aquatic macrophytes | No data | Craig, 2000 |
43 | Spawning depth | Shallow water | No data | Bruslé and Quignard, 2001 |
43 | Spawning depth | Often moves from deep to shallow areas to spawn | No data | Crosier et al, 2005 |
43 | Spawning depth | Shallow waters, usually less than 3 meters | 3.0 m | Ogle, 1998 |
43 | Spawning depth | Most spawning occurs at a depth of less than 1 m | 1.0 m | Leino and McCormick, 1997 |
43 | Spawning depth | Shallow water | No data | Environment agency, ??? |
43 | Spawning depth | Shallow waters | No data | Maitland, 1977 |
44 | Spawning substrate | Spawn on occurs on a variety of substrates : open-substrate, phytolithophil, submerged plants, logs, branches, or gravel or rocks but also hard bottoms, sand, clay, or gravel | Lithophils | Ogle, 1998 |
44 | Spawning substrate | Ribbons are winded up aquatic plants | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Submerged plants, logs, branches, rocks | Phytophils | Crosier et al, 2005 |
44 | Spawning substrate | Stones and vegetation | Lithophils | Craig, 2000 |
44 | Spawning substrate | Plants, or gravel | Lithophils | Crivelli and Rosecchi, 2001 |
44 | Spawning substrate | Eggs adhere to sumerged plants, bit other substrata are utilised if suitable plants are absent, <5 cm in diameter | Phytophils | Mann, 1996 |
44 | Spawning substrate | Stones and weed | Phytophils | Environment agency, ??? |
44 | Spawning substrate | Phytolithophil | Lithophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Phyto-lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Stones and plants | Phytophils | Maitland, 1977 |
45 | Spawning site preparation | Eggs are deposited on plants or rocks | Susbtrate chooser | Billard, 1997 |
45 | Spawning site preparation | Open water/ substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Mann, 1996 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
48 | Spawning release | More than one clutches of eggs per spawning season, intermittent spawner | Fractional | Leino and McCormick, 1997 |
48 | Spawning release | Eggs are extruted in long adhesive and 'accordion folded' strands | No category | Billard, 1997 |
48 | Spawning release | Female spawn several batches during the spawning season | Multiple | Crivelli and Rosecchi, 2001 |
48 | Spawning release | Intermittent spawner with prolonged spawning season | Fractional | Saat and Veersalu, 1996 |
48 | Spawning release | Eggs are extruted in long adhesive and 'accordion folded' strands like perch ??? | No category | Spillmann, 1961 |
48 | Spawning release | Ruffle eggs are extruded in "strands" ? Never observed anywhere else | No category | Ogle, 1998 |
48 | Spawning release | 1000-6000 by batch, in a form of a ribbon | Multiple | Bruslé and Quignard, 2001 |
48 | Spawning release | Females may spawn two or more batches of eggs in a season, one in winter-spring and one later in summer. Spawnings occurs intermittently, with eggs being laid in two or more batches per year | Multiple | Crosier et al, 2005 |
48 | Spawning release | Intermittent spawners: eggs are laid in two or more batches | Multiple | Craig, 2000 |
48 | Spawning release | Spawing is prolonged and portional, the eggs being laid in two or three portions | No category | Neja, 1988 |
48 | Spawning release | The analysis indicated that an average ruffe in all heated areas produced three mature portions of eggs during the spawing season, compard with two in the reference area | No category | Luksiene et al, 2000 |
48 | Spawning release | In asynchronous spawners like ruffe, egg size in consecutive batches is found to be smaller, which is associated with the diminishing resources of the female | Multiple | Albert et al, 2006 |
49 | Parity | Female ruffe may reach age 11, but male ruffe generally do not exceed age 7 | No category | Ogle, 1998 |
49 | Parity | The prolonged spawning period is possibly due to different rates of development of the ovaries among females of different ages | No category | Brown et al, 1998 |
49 | Parity | Most individuals atain a maximum age of 6 years, excepeionally 7 or 8 years | No category | Kovac, 1998 |
50 | Parental care | Non-guarding | No care | Ogle, 1998 |
50 | Parental care | Non-guarders | No care | Fishbase, 2006 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |