Trait completeness | 96% |
Total data | 267 |
References | 41 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 0.80 to 1.00-1.12 [Ooocytes prior to spawning] | 1.06 mm | Brylinska et al, 2002 |
1 | Oocyte diameter | 0.96-1.14 | 1.05 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | Slightly above 1 | 1.0 mm | Spillmann, 1961 |
1 | Oocyte diameter | 1.0 | 1.0 mm | Persat, 2001 |
1 | Oocyte diameter | 0.5 before extrusion, but up to 1.25 and 1.77 | 0.5 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | Small: 0.95-1.15 | 1.05 mm | Kujawa et al, 2002 |
2 | Egg size after water-hardening | 0.5-1.70 [Not specified] | 1.1 mm | Brylinska et al, 2002 |
2 | Egg size after water-hardening | 1.25-1.77 [Not precised] | 1.51 mm | Mellinger, 2002 |
2 | Egg size after water-hardening | 0.5-1.7 [Mode 0.9] | 1.1 mm | Fishbase, 2006 |
2 | Egg size after water-hardening | 0.8-1.2 [Seems to be fertilized eggs] | 1.0 mm | Bonislawska et al, 2001 |
3 | Egg Buoyancy | Semi-buoyant [easily transported by slight water movements] | Pelagic | Van Houdt, 2003 |
3 | Egg Buoyancy | Demersal, and carried by the current | Demersal | Bruslé and Quignard, 2001 |
3 | Egg Buoyancy | Semi-pelagic, fall slowly on the ground | Pelagic | Persat, 2001 |
3 | Egg Buoyancy | On the bottom, demersal | Demersal | Fishbase, 2006 |
3 | Egg Buoyancy | Semibuoyant | Pelagic | Hudd and Kjellman, 2002 |
3 | Egg Buoyancy | Eggs are semi-buoyant when first laid, but become demersal within a few days and settle into interstices into the substrate | Demersal | Bradbury et al, 1999 |
3 | Egg Buoyancy | The eggs are semipelagic (partially float) and sink slowly to the bottom | Pelagic | Anonymous, 2003 |
3 | Egg Buoyancy | Eggs are demersal, but the presence of a large fat droplet makes the eggs remain near the bottom in a suspended condition | Demersal | Kirillov, 1989 |
3 | Egg Buoyancy | Eggs develop inthe water column, but others described it at on the bottom. 24 hours after fertilisation eggs sink to the bottom. Before sinking eggs are transported downstream with water. At water current speed of 0.2 m/s eggs sink to the bottom and remain. On the rough ground, at the current speed of 4 m/s eggs start to float, and all eggs are washed out by a water current of 8 m/s | Demersal | Kujawa et al, 2002 |
3 | Egg Buoyancy | Semi-buoyant eggs settle to the bottom in quiet water; may be carried from spawning site by slight current | Demersal | Goodyear et al. et al, 1982 |
4 | Egg adhesiveness | Not sticky, free on the ground | Non-Adhesive | Spillmann, 1961 |
4 | Egg adhesiveness | Free, then stick to the ground | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Free on the ground | Non-Adhesive | Billard, 1997 |
4 | Egg adhesiveness | Not sticky | Non-Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Egg stickiness is weak | Adhesive | Kujawa et al, 2002 |
4 | Egg adhesiveness | non-adhesive | Non-Adhesive | Goodyear et al. et al, 1982 |
5 | Incubation time | 30-60 | 45.0 days | Persat, 2001 |
5 | Incubation time | 30 days at 5.5°C | 30.0 days | Scott and Crossman, 1973 |
5 | Incubation time | 30 [6.1°C], 71 [0-3.6°C] | 1.8 days | Fishbase, 2006 |
5 | Incubation time | Eggs incubate for 3-4 months | 3.5 days | Bradbury et al, 1999 |
5 | Incubation time | Takes about 30 days to hatch | 30.0 days | Anonymous, 2003 |
5 | Incubation time | Last about 3 months at 1°C, also described as 27-60 days, 77-78 days. | 43.5 days | Kujawa et al, 2002 |
5 | Incubation time | Eggs hatch in 30 days at 43°F | 30.0 days | Goodyear et al. et al, 1982 |
6 | Temperature for incubation | 5.5 | 5.5 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 0-6.1 | 3.05 °C | Fishbase, 2006 |
6 | Temperature for incubation | 0-2 | 1.0 °C | Hudd and Kjellman, 2002 |
6 | Temperature for incubation | At a mean temperature of incubation of 3.5°C, burbot hatched after 30 days 3 hours. Eggs of burbot can be incubated in Weiss jars at 0.5 to 3.5°C. During the first week of incubation water temperature can not exceed 4-5°C | 4.5 °C | Kujawa et al, 2002 |
6 | Temperature for incubation | Embryonic development occurs within a narrow temperature range of 2-6°C | 4.0 °C | Harzevili et al, 2004 |
7 | Degree-days for incubation | 112-200 | 156.0 °C * day | Van Houdt, 2003 |
7 | Degree-days for incubation | 200 | 200.0 °C * day | Spillmann, 1961 |
7 | Degree-days for incubation | 200 | 200.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 150 | 150.0 °C * day | Scott and Crossman, 1973 |
7 | Degree-days for incubation | 180-200 | 190.0 °C * day | Fishbase, 2006 |
7 | Degree-days for incubation | Mass hatching occur at 117-131 | 124.0 °C * day | Hudd and Kjellman, 2002 |
7 | Degree-days for incubation | 80-200, also descried as 109.4 | 140.0 °C * day | Kujawa et al, 2002 |
3 | Egg Buoyancy | Demersal | Demersal | McPhail and Paragamian, 2000 |
3 | Egg Buoyancy | Demersal | Demersal | Chen, 1969 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | Chen, 1969 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | McPhail and Paragamian, 2000 |
2 | Egg size after water-hardening | 0.71-1.70 | 1.21 mm | McPhail and Paragamian, 2000 |
6 | Temperature for incubation | 4 | 4.0 °C | Donner et al, 2011 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 3-4 | 3.5 mm | Persat, 2001 |
8 | Initial larval size | 3 | 3.0 mm | Mittelbach and Persson, 1998 |
8 | Initial larval size | Range from 3.5-3.9, depending of egg diameter, sporadically newly hatched larvae attain 4.3. mm | 3.7 mm | Kujawa et al, 2002 |
9 | Larvae behaviour | Pelagic until 6-7 mm then become benthic | Pelagic | Bruslé and Quignard, 2001 |
9 | Larvae behaviour | Small pelagic larvae | Pelagic | Van Houdt, 2003 |
9 | Larvae behaviour | Pelagic, gregarious, steadily remain under the surface of water | Pelagic | Persat, 2001 |
9 | Larvae behaviour | At hatching, the offspring are at first pelagic, threafter they are found in shallow littoral waters | Pelagic | Hudd and Kjellman, 2002 |
9 | Larvae behaviour | Buoyant larvae are carried downstream in water currents | Demersal | Mann, 1996 |
9 | Larvae behaviour | Immediate dispersion after hatching | Demersal | Urho, 2002 |
9 | Larvae behaviour | Upon hatching larvae are pelagic | Pelagic | Bradbury et al, 1999 |
9 | Larvae behaviour | Dispersed earlier at the yolk-stage and ended up in the littoral | Demersal | Urho, 1996 |
9 | Larvae behaviour | Newly hatched larvae repeatedly swim up and sink, later they sink to the bottom where they remain until final resoprtion of yolk sac. When a major part of the yolk sac is resorbed fish start swimming searching for food. They aggregate in the surface layers of shallow waters, where they fed on phytoplankton and rotifers. | Demersal | Kujawa et al, 2002 |
10 | Reaction to light | Survival data reveal that burbot larvae survive better under light condition compared with dark. […] a positive reaction to light by burbot larvae would be replaced by a negative phototactic at the later stage of development. | Photopositive | Harzevili et al, 2004 |
11 | Temperature during larval development | Water temperature was constant during rearing | No data | Harzevili et al, 2003 |
11 | Temperature during larval development | Range from 10-11°C for the apperance of erythrocytes to 13°C for the onset of active swimming, and 15-16°C for the beginning of feeding | 10.5 °C | Kujawa et al, 2002 |
11 | Temperature during larval development | Five constant temperatures of 12, 15, 18, 21 and 24°C (range ± 0.5°C), all in duplicate, were employed in the experiment. The fastest larval growth, either in terms of total length or body weight, was recorded for the temperature of 21°C, whereas at 12°C the larvae grew the slowest. A final survival rate of at least 90% was observed for the burbot reared at 12 and 15°C; this figure was significantly higher than at the other water temperatures. The fish reared at 12°C had the second highest survival rate at 72%. | 12.0 °C | Wolnicki et al, 2002 |
11 | Temperature during larval development | Food intake by burbot larvae begins when water temperature is above 8°C. […] larvae could tolerate up to a temperature of 20°C. The temperature of spring water was 12 ± 1°C upon release of the larvae but gradually adjusted to 16 and 20°C. […] High survival of burbot larvae at a higher temperature in the first 10 days of the experiment suggests that embryos (incubation temperature before the hatching was 4 ± 1°C) and larvae differ in their physiological tolerances. [...] It seems that the most appropriate temperature for successful burbot larvae culture is ranged between 12 and 16°C, and represents a trade-off between faster growth with higher mortalities at higher temepratures and slow growth, but higher survival at lower temperatures. | 12.0 °C | Harzevili et al, 2004 |
11 | Temperature during larval development | As evidenced by these results, a temperature of 21°C would be closest to the optimum growth temperature (OGT) for larvae of this species. The results presented here also indicate that a temperature of 18°C or lower and particularly 24°C are out of the optimal range for larval burbot because of either relatively slow fish growth or unsatisfactory survival or both | 21.0 °C | Wolnicki et al, 2002 |
12 | Sibling intracohort cannibalism | Sibling intracohort cannibalism is present | Present | Kujawa et al, 2002 |
12 | Sibling intracohort cannibalism | No cannibalism occurred at any temperature throughout the experiment, although in this species it may appear at about 12 mm TL | Absent | Wolnicki et al, 2002 |
13 | Full yolk-sac resorption | Yolk-feeding burbot larvae resorb their yolk sac during almost two weeks after hatching | No data | Kujawa et al, 2002 |
13 | Full yolk-sac resorption | At the yolk stage they measure 3-4 mm. | 3.5 °C * day | Harzevili et al, 2004 |
14 | Onset of exogeneous feeding | 270 DD at 15-16°C after fertilization, they begin feeding less than about 130-140 DD for incubation | 15.5 °C * day | Kujawa et al, 2002 |
14 | Onset of exogeneous feeding | Burbot larvae, which were the pooled offpsring of many wild spawners, were reared from the first feeding (day 10 post-hatch) over a period of 20 days. Larvae of an initial size of 3.61 ± 0.27 mm (average TL ± SD; n = 15). | 3.61 °C * day | Wolnicki et al, 2002 |
10 | Reaction to light | photopositive until 40 mm long | Photopositive | McPhail and Paragamian, 2000 |
8 | Initial larval size | 3.47 +/- 0.09 | 3.47 mm | Taylor, 2001 |
8 | Initial larval size | 3.97 | 3.97 mm | Palinska-Zarska, 2014 |
9 | Larvae behaviour | Pelagic for 3 months after hatching then switch to benthic | Pelagic | Donner et al, 2011 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4+ | 4.0 year | Van Houdt, 2003 |
15 | Age at sexual maturity | 3 | 3.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | Usually in the 3-4 [Both sex] | 3.5 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | 4 | 4.0 year | Fishbase, 2006 |
15 | Age at sexual maturity | 7+ [Lowest age] | 7.0 year | Vedeneev et al, 2003 |
15 | Age at sexual maturity | In Canada, burbot generally reach sexual maturity between 2-8 years of age [sex not specified] | 5.0 year | Bradbury et al, 1999 |
15 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 year | Anonymous, 2003 |
15 | Age at sexual maturity | Some burbot are probably sexuallu mature when 2 years old, and immaturity seems to be associated more with size than with age | 2.0 year | Hewson, 1955 |
15 | Age at sexual maturity | First spawning females are 4 years old, a year older than males | 4.0 year | Kujawa et al, 2002 |
15 | Age at sexual maturity | Burbot matured in Lake Cle Elum at 2-4 years (28-43 cm TL). In Palmer Lake, all mature males were six years or older and mature females seven years or older (54 and 64 cm TL, respectively). Most burbot matured at 3-4 years of age in three Wyoming lakes, and two years in Lake Winninpeg | 3.0 year | Bonar et al, 2000 |
16 | Length at sexual maturity | 32-34 [Sex not specified] | 33.0 cm | Van Houdt, 2003 |
16 | Length at sexual maturity | 30-40 | 35.0 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | 28-48 [Both sex] | 38.0 cm | Scott and Crossman, 1973 |
16 | Length at sexual maturity | 35-40 | 37.5 cm | Fishbase, 2006 |
16 | Length at sexual maturity | 65 [Lowest size] | 65.0 cm | Vedeneev et al, 2003 |
16 | Length at sexual maturity | 28-48 [Sex not specified] | 38.0 cm | Anonymous, 2003 |
16 | Length at sexual maturity | 16.2 [Age 3], 19.3 [Age 4], 20.7 [Age 5] both sex in Winnipeg Beach | 16.2 cm | Hewson, 1955 |
16 | Length at sexual maturity | Mean 57, range 45.5-77 [Age 6+], Mean 55.4, range 49-75 [Age 7+], and mean 71.3, range 55-87 [Age 8+] | 61.25 cm | Kirillov, 1989 |
16 | Length at sexual maturity | The mean length of mature males and females was the same 49 ± 3 cm | 49.0 cm | Pulliainen and Korhonen, 1990 |
16 | Length at sexual maturity | Mean of 22.95, range 21.2-25.9 for females studied | 23.55 cm | Banbura and Koszalinski, 1991 |
16 | Length at sexual maturity | Burbot mature at a length of 30 cm [Sex not specified] | 30.0 cm | Kujawa et al, 2002 |
16 | Length at sexual maturity | The length of adult burbot is normally in the range 300-500 mm | 400.0 cm | Slavik and Bartos, 2002 |
17 | Weight at sexual maturity | 2.5 [Lowest weight] | 2.5 kg | Vedeneev et al, 2003 |
17 | Weight at sexual maturity | 1.3 pounds [Age 3], 2.2 [Age 4], 2.4 [Age 5] both sex in Winnipeg Beach. The largest immature female weighed 1.5 pounds | 1.3 kg | Hewson, 1955 |
17 | Weight at sexual maturity | Mean 1.724, range 0.62-3.73 [Age 6+], Mean 2.53, range 0.8-3.12 [Age 7+], and mean 3.080, range 1.1-6.1 [Age 8+] | 2.17 kg | Kirillov, 1989 |
17 | Weight at sexual maturity | Burbot matured in Lake Cle Elum at 2-4 years (28-43 cm TL). In Palmer Lake, all mature males were six years or older and mature females seven years or older (54 and 64 cm TL, respectively). Most burbot matured at 3-4 years of age in three Wyoming lakes, and two years in Lake Winninpeg | 3.0 kg | Bonar et al, 2000 |
18 | Female sexual dimorphism | Females reach maturity at a lesser weight than males, possibly younger | Absent | Hewson, 1955 |
19 | Relative fecundity | 448.8-1234.5 | 841.65 thousand eggs/kg | Brylinska et al, 2002 |
19 | Relative fecundity | 400-1000 | 700.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 1000 | 1000.0 thousand eggs/kg | Spillmann, 1961 |
19 | Relative fecundity | 500-1000 | 750.0 thousand eggs/kg | Van Houdt, 2003 |
19 | Relative fecundity | 617.9-1572 | 1094.95 thousand eggs/kg | Brylinska et al, 2002 |
19 | Relative fecundity | 1000 | 1000.0 thousand eggs/kg | Persat, 2001 |
19 | Relative fecundity | 49 | 49.0 thousand eggs/kg | Mittelbach and Persson, 1998 |
19 | Relative fecundity | 1000 | 1000.0 thousand eggs/kg | Kunz, 2004 |
19 | Relative fecundity | 957.48 ± 180.27 | 957.48 thousand eggs/kg | Banbura and Koszalinski, 1991 |
20 | Absolute fecundity | 32.2-1453 | 742.6 thousand eggs | Brylinska et al, 2002 |
20 | Absolute fecundity | 33-5000 | 2516.5 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | From 45.6 for a 343-mm female to 1,362.077 to a 643-mm female | 45.6 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | Mean 1417, from 1014 to 2383 | 1417.0 thousand eggs | Vedeneev et al, 2003 |
20 | Absolute fecundity | The maximum absolute fecundity in the Vilyuysk Reservoir is 777000, individual absolute fecundity of Ob' burbot reaches 5 million eggs | 777000.0 thousand eggs | Kirillov, 1989 |
20 | Absolute fecundity | Mean of 89 692, range 60 728-159 613 | 443.5 thousand eggs | Banbura and Koszalinski, 1991 |
20 | Absolute fecundity | A female produces 10000-800000, up to 5000000 | 405000.0 thousand eggs | Kujawa et al, 2002 |
20 | Absolute fecundity | 300-400 | 350.0 thousand eggs | Billard, 1997 |
20 | Absolute fecundity | Mean of 324 [From 230-430] | 330.0 thousand eggs | Vedeneev et al, 2003 |
22 | Onset of oogenesis | July [Increase from July to November] | ['July', 'August', 'September', 'October', 'November'] | Brylinska et al, 2002 |
22 | Onset of oogenesis | August | ['August'] | Pulliainen and Korhonen, 1990 |
22 | Onset of oogenesis | The onset of ovarian recrudescence was first evident in early June | ['June'] | June, 1977 |
23 | Intensifying oogenesis activity | November-December | ['November', 'December'] | Pulliainen and Korhonen, 1990 |
23 | Intensifying oogenesis activity | November-December | ['November', 'December'] | June, 1977 |
24 | Maximum GSI value | 8.8 (November 26) but also up to 16.9% | 8.8 percent | Brylinska et al, 2002 |
24 | Maximum GSI value | Mean of 12, from 10-14.8 in December [Coefficient of sexual maturation] | 12.4 percent | Vedeneev et al, 2003 |
24 | Maximum GSI value | 10-11 [In beginning of January] | 10.5 percent | June, 1977 |
25 | Oogenesis duration | 5-6 [From July to November] | 5.5 months | Brylinska et al, 2002 |
26 | Resting period | 0.5 -1.3 [July 29] | 2.0 months | Brylinska et al, 2002 |
26 | Resting period | April to August | 6.0 months | Pulliainen and Korhonen, 1990 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3+ | 3.0 years | Van Houdt, 2003 |
27 | Age at sexual maturity | 1-2 | 1.5 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | Usually in the 3-4 [Both sex] | 3.5 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | 3.0 | 3.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | 5 [Lowest age] | 5.0 years | Vedeneev et al, 2003 |
27 | Age at sexual maturity | In Canada, burbot generally reach sexual maturity between 2-8 years of age [sex not specified] | 5.0 years | Bradbury et al, 1999 |
27 | Age at sexual maturity | 3-4 [Sex not specified] | 3.5 years | Anonymous, 2003 |
27 | Age at sexual maturity | Some burbot are probably sexually mature when 2 years old, and immaturity seems to be associated more with size than with age | 2.0 years | Hewson, 1955 |
27 | Age at sexual maturity | Burbot attain sexual maturity in the Vilyuy basin in the 7th year, mostly 8th of life. Most probably, the males mature one year earlier | 7.0 years | Kirillov, 1989 |
27 | Age at sexual maturity | First spawning males are 3 years old | 3.0 years | Kujawa et al, 2002 |
27 | Age at sexual maturity | Burbot matured in Lake Cle Elum at 2-4 years (28-43 cm TL). In Palmer Lake, all mature males were six years or older and mature females seven years or older (54 and 64 cm TL, respectively). Most burbot matured at 3-4 years of age in three Wyoming lakes, and two years in Lake Winninpeg | 3.0 years | Bonar et al, 2000 |
28 | Length at sexual maturity | 32-34 [sex not specified] | 33.0 cm | Van Houdt, 2003 |
28 | Length at sexual maturity | 28.0-48.0 [For female but males usually mature at a smaller size] | 38.0 cm | Scott and Crossman, 1973 |
28 | Length at sexual maturity | 27-30 | 28.5 cm | Fishbase, 2006 |
28 | Length at sexual maturity | 51 [Lowest size] | 51.0 cm | Vedeneev et al, 2003 |
28 | Length at sexual maturity | 28-48 [Sex not specified] | 38.0 cm | Anonymous, 2003 |
28 | Length at sexual maturity | 16.2 [Age 3], 19.3 [Age 4], 20.7 [Age 5] both sex in Winnipeg Beach | 16.2 cm | Hewson, 1955 |
28 | Length at sexual maturity | Mean 56.1, range 46.5-71 [Age 6+], mean 57.5, range 49.5-77 [Age 7+] | 58.75 cm | Kirillov, 1989 |
28 | Length at sexual maturity | The mean length of mature males and females was the same 49 ± 3 cm | 49.0 cm | Pulliainen and Korhonen, 1990 |
28 | Length at sexual maturity | Burbot mature at a length of 30 cm [Sex not specified] | 30.0 cm | Kujawa et al, 2002 |
28 | Length at sexual maturity | Burbot matured in Lake Cle Elum at 2-4 years (28-43 cm TL). In Palmer Lake, all mature males were six years or older and mature females seven years or older (54 and 64 cm TL, respectively). Most burbot matured at 3-4 years of age in three Wyoming lakes, and two years in Lake Winninpeg | 35.5 cm | Bonar et al, 2000 |
29 | Weight at sexual maturity | 0.9 [Lowest weight] | 0.9 kg | Vedeneev et al, 2003 |
29 | Weight at sexual maturity | The largest immature male weighed 2.2 pounds | 2.2 kg | Hewson, 1955 |
29 | Weight at sexual maturity | Mean 1.381, range 0.8-3.065 [Age 6+], and mean 1.411, range 0.85-3.56 [Age 7+] | 1.93 kg | Kirillov, 1989 |
30 | Male sexual dimorphism | GSI in burbot is higher for the testes than the ovaries !!! | Absent | Brylinska et al, 2002 |
31 | Onset of spermatogenesis | July [Increase from July to November] | ['July', 'August', 'September', 'October', 'November'] | Brylinska et al, 2002 |
31 | Onset of spermatogenesis | Slight increase in June, clear increase in November | ['June', 'November'] | Pulliainen and Korhonen, 1990 |
32 | Main spermatogenesis activity | October-November | ['October', 'November'] | Pulliainen and Korhonen, 1990 |
33 | Maximum GSI value | 20.6 [November 26] but up to 25.8% | 20.6 percent | Brylinska et al, 2002 |
33 | Maximum GSI value | Mean of 11.1, from 9.5-16.0 in December [Coefficient of sexual maturation] | 12.75 percent | Vedeneev et al, 2003 |
33 | Maximum GSI value | The maturity index of males sharply increases in November to 14.55 | 14.55 percent | Kirillov, 1989 |
35 | Resting period | 0.5-2.7 [July 29th] | 1.6 months | Brylinska et al, 2002 |
35 | Resting period | No difference in term of GSI between April and July, and even up to October | 6.0 months | Pulliainen and Korhonen, 1990 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Spawning is often preceed by a spawning migration over long distances: sometimes up to 400 km [but could be less than 10 km] | 400.0 km | Van Houdt, 2003 |
36 | Spawning migration distance | About 60-70 km | 65.0 km | Vedeneev et al, 2003 |
36 | Spawning migration distance | If possible lacustrine populations migrate to rivers for spawning. Burbot from Baikal Lake migrate several hundreds km to spawning grounds in rivers | No data | Kujawa et al, 2002 |
37 | Spawning migration period | The spawning migration began from the second half of October and continued until early January, i.e. in the period of the open water followed by the period of ice | ['January', 'October'] | Vedeneev et al, 2003 |
37 | Spawning migration period | They travel upstream 1.5-2 km (maximally 6 km per day), migration lasts 5-6 months (from September to January). Spawning migration are triggered by a decrease of water temperature in the lake 10-12°C. | ['January', 'September', 'October', 'November'] | Kujawa et al, 2002 |
37 | Spawning migration period | Move from deep water to nearshore areas and into harbors and rivers, usually beginning in early November | ['November'] | Goodyear et al. et al, 1982 |
38 | Homing | Migrate to their "home stream" every year | Present | Van Houdt, 2003 |
39 | Spawning season | December-January | ['January', 'December'] | Billard, 1997 |
39 | Spawning season | November to March [In February in Alpin lakes] | ['January', 'February', 'March', 'November'] | Bruslé and Quignard, 2001 |
39 | Spawning season | During winter [February in France] | ['January', 'February', 'March'] | Spillmann, 1961 |
39 | Spawning season | November to March | ['January', 'February', 'March', 'November'] | Van Houdt, 2003 |
39 | Spawning season | Spawns in mid-winter under the ice: from November to May, but mainly in January to March in Canada | ['January', 'February', 'March', 'April', 'May', 'November'] | Scott and Crossman, 1973 |
39 | Spawning season | Mainly in December to January [But from November to March] | ['January', 'February', 'March', 'November', 'December'] | Fishbase, 2006 |
39 | Spawning season | From late December to January | ['January', 'December'] | Vedeneev et al, 2003 |
39 | Spawning season | Spawn in February and March in Northern Finland | ['February', 'March'] | Pulliainen and Korhonen, 1993 |
39 | Spawning season | November-March | ['March', 'November'] | Mann, 1996 |
39 | Spawning season | End of November to Beginning of March | ['March', 'November'] | Terver, 1984 |
39 | Spawning season | Spawn under the ice, usually between January and March | ['January', 'February', 'March'] | Bradbury et al, 1999 |
39 | Spawning season | Spawn in midwinter under the ice, from November to May, but generally they spawn in Janaury through March | ['January', 'February', 'March', 'April', 'May', 'November'] | Anonymous, 2003 |
39 | Spawning season | Male burbot were observed in a near-ripe condition about January 20 in each year, and actual spawning probably commenced about January 31. Many fish were spent by February 10, but ripe unspawned fish of both sex occurred as late as February 20. | ['January', 'February'] | Hewson, 1955 |
39 | Spawning season | Maximum feeding of burbot was observed during the prespawning (September-December) and postspawning (March-June) feeding periods | ['March', 'June', 'September', 'December'] | Kirillov, 1989 |
39 | Spawning season | In 1987, spawning males were found from 13 March to 5 April and females from 2 March to 27 March, whereas in 1988 spawning occurred earlier: from 26 February to 20 March in the males and from 11 February to 11 march in the females. | ['February', 'March', 'April'] | Pulliainen and Korhonen, 1990 |
39 | Spawning season | From December to Marhc | ['December'] | Kujawa et al, 2002 |
39 | Spawning season | Mean peak spawning 14 January [Range: 12 January-1 February] in Lake Oahe, South and North Dakota | ['January', 'February'] | June, 1977 |
39 | Spawning season | Winter spawner. In the lakes of North America, activity of burbot increased until the period of reproduction in February and March | ['January', 'February', 'March'] | Slavik and Bartos, 2002 |
39 | Spawning season | A 1-week period in november-May, at 33-50°F; varies considerably with locality; eggs have also been collected in September | ['May', 'September'] | Goodyear et al. et al, 1982 |
39 | Spawning season | Burbot spawn in winter time at a temperature of 1-4°C | ['January', 'February', 'March'] | Harzevili et al, 2004 |
39 | Spawning season | Burbot spawn in the winter or early spring in most areas | ['January', 'February', 'March', 'April', 'May', 'June'] | Bonar et al, 2000 |
40 | Spawning period duration | Males are usually present first in the spawning area | No data | Van Houdt, 2003 |
40 | Spawning period duration | Males arrive on the spawning ground first, followed in 3 or 4 days by the female | 3.0 weeks | Scott and Crossman, 1973 |
40 | Spawning period duration | 4-5 [From late December to January] | 4.5 weeks | Vedeneev et al, 2003 |
40 | Spawning period duration | Males reach spawning grounds first and females follow a couple of days later | No data | Anonymous, 2003 |
40 | Spawning period duration | Lasts about 3 weeks | 3.0 weeks | Hewson, 1955 |
40 | Spawning period duration | During 7-10 days males are able to fertilize eggs produced by subsequently arriving females. In controlled conditions, milt preserves its fertilizing capacity during a month. | 8.5 weeks | Kujawa et al, 2002 |
40 | Spawning period duration | 1 one week period | 1.0 weeks | Goodyear et al. et al, 1982 |
41 | Spawning temperature | 5-10 | 7.5 °C | Spillmann, 1961 |
41 | Spawning temperature | 0.5-4 | 2.25 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 0.5-4 | 2.25 °C | Van Houdt, 2003 |
41 | Spawning temperature | 1.0 | 1.0 °C | Billard, 1997 |
41 | Spawning temperature | <5°C | 5.0 °C | Persat, 2001 |
41 | Spawning temperature | Usually 0.6-1.7°C | 1.15 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | < 4 | 4.0 °C | Mann, 1996 |
41 | Spawning temperature | 0.5-4.0 | 2.25 °C | Mittelbach and Persson, 1998 |
41 | Spawning temperature | Burbot spawn in winter time at a temperature of 1-4°C | 2.5 °C | Harzevili et al, 2004 |
41 | Spawning temperature | 33-50°F | 41.5 °C | Goodyear et al. et al, 1982 |
42 | Spawning water type | "Bras morts ou les annexes inondées en rivières" , 2-3 m in lakes | Stagnant water | Persat, 2001 |
42 | Spawning water type | Shallow bays, usually spawn in the lake they are also know to move into rivers to spawn | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Lakes or rivers | Stagnant water | Vedeneev et al, 2003 |
42 | Spawning water type | Both lakes and rivers | Stagnant water | Bradbury et al, 1999 |
42 | Spawning water type | Spawning condition occurred both inshore and offshore, but they were observed in greater numbers in the inshore nets | Stagnant water | Hewson, 1955 |
42 | Spawning water type | Typically in river beds. Spawning in lakes was reported as well. A part of burbot lacustrine populations in Sweden spawned in the lakes | Stagnant water | Kujawa et al, 2002 |
42 | Spawning water type | Nearshore areas, including shorelines, river mouths, bays, and harbors; offshore bars and reefs; swift, open water in streams | Stagnant water | Goodyear et al. et al, 1982 |
42 | Spawning water type | Burbot can spawn either in lakes or rivers. In washington, burbot evidently spawn in lakes and reservoirs except for some Lake Roosevelt fish that spawn in a flowing section of the Columbia River near the Canadian border | Stagnant water | Bonar et al, 2000 |
43 | Spawning depth | Sometimes quite deep in lakes | No data | Spillmann, 1961 |
43 | Spawning depth | Shallow water: 2-3 deep | 2.5 m | Van Houdt, 2003 |
43 | Spawning depth | 0.5-1.5 [2-3 m in lakes] | 2.5 m | Persat, 2001 |
43 | Spawning depth | Usually at 0.3-1.20 m (1-4 feet) of water, but circumstantial evidence that burbit spawn in deep water | 0.75 m | Scott and Crossman, 1973 |
43 | Spawning depth | In lakes, spawning occurs in areas with little accumulation of silt or detritus, usually at depths of 0.3-3.0 m, but has been reported at depths of 18-20 m | 1.65 m | Bradbury et al, 1999 |
43 | Spawning depth | The spawning act was accomplished near the surface | No data | Hewson, 1955 |
43 | Spawning depth | Shallow lakes with well oxygenated water are selected by burbot for spawning | No data | Kujawa et al, 2002 |
43 | Spawning depth | 1-480 feet, bh deepwater and shallow-water are reported | 240.5 m | Goodyear et al. et al, 1982 |
44 | Spawning substrate | Clear substrate of sand or gravel | Lithophils | Van Houdt, 2003 |
44 | Spawning substrate | Sand or gravels | Lithophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Clear gravels | Lithophils | Spillmann, 1961 |
44 | Spawning substrate | Sand or gravel bottom | Lithophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Gravel and sandy sites | Lithophils | Vedeneev et al, 2003 |
44 | Spawning substrate | Stones/gravels | Lithophils | Mann, 1996 |
44 | Spawning substrate | Litho-pelagophil | Pelagophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Litho-pelagophil | Pelagophils | Balon, 1975 |
44 | Spawning substrate | Over clean sand, gravel or cobble/rubble substrates | Lithophils | Bradbury et al, 1999 |
44 | Spawning substrate | Over rocky susbtrates | Lithophils | Anonymous, 2003 |
44 | Spawning substrate | Spawning grounds of burbot are typically river beds covered with stones and gravel | Lithophils | Kujawa et al, 2002 |
44 | Spawning substrate | Eggs are scattered in mid-water over rock, gravel, shale, sand, clay, or mud | Lithophils | Goodyear et al. et al, 1982 |
45 | Spawning site preparation | No nest is built | Open water/substratum scatter | Scott and Crossman, 1973 |
45 | Spawning site preparation | Open water/substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | No, eggs are laid on stones/gravels | Susbtrate chooser | Mann, 1996 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
45 | Spawning site preparation | Eggs are broadcast into the water column well above the substrate | Susbtrate chooser | Bradbury et al, 1999 |
45 | Spawning site preparation | No nest is built | Open water/substratum scatter | Ah-King et al, 2004 |
45 | Spawning site preparation | No nests are built | Open water/substratum scatter | Anonymous, 2003 |
46 | Nycthemeral period of oviposition | Always occur at night | Night | Van Houdt, 2003 |
46 | Nycthemeral period of oviposition | Night | Night | Persat, 2001 |
46 | Nycthemeral period of oviposition | Spawning activity takes place only at night and the grounds are deserted in the daytime | Day | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | Occurs at night | Night | Anonymous, 2003 |
46 | Nycthemeral period of oviposition | Burbot spawners avoid strong light, typically they spawn at night | Night | Kujawa et al, 2002 |
47 | Mating system | Communal process, up to 20 or so individuals | Promiscuity | Van Houdt, 2003 |
47 | Mating system | The actual spawning activity is said to take place at in a writhing ball about 2 feet in diameter, which moves over the bottom and is made up of 10-12 intertwined and constantly moving individuals | No category | Scott and Crossman, 1973 |
47 | Mating system | Pairspawning for Lota lota lota and by group for Lota lota maculosa: group spawn, a tangled globular mass of moving males and females, spawing 10-12 ind interwined | Promiscuity | Ah-King et al, 2004 |
47 | Mating system | Spawning activity is quite a sight. They are known to form writhing masses of 10-12 constantly moving individuals that can get as large as 2 feet in diameter. This writhing mass of spawners moves over the bottom and frop eggs. | No category | Anonymous, 2003 |
48 | Spawning release | One clear seasonal peak per year | Total | Fishbase, 2006 |
49 | Parity | Spawning may not repeat every year | Iteroparous | Vedeneev et al, 2003 |
49 | Parity | Can live up to 10 to 15 years | No category | Anonymous, 2003 |
49 | Parity | Some mature fish do not spawn every year | Iteroparous | Hewson, 1955 |
49 | Parity | Burbot spending a rest year do not accumulate and store energy reserves over the summer for the next year, and that such rest years, if they exist, do not occur for nuttritional reasons | No category | Pulliainen and Korhonen, 1990 |
49 | Parity | After spawning, fish migrate downstream to lakes | No category | Kujawa et al, 2002 |
49 | Parity | Usually return to deeper water by April; may remain in harbors until mid-June before moving into lakes; often move from lakes into rivers after spawning | Iteroparous | Goodyear et al. et al, 1982 |
50 | Parental care | No care is given to the young | No care | Scott and Crossman, 1973 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |
50 | Parental care | No parental care | No care | Ah-King et al, 2004 |