Trait completeness | 86% |
Total data | 152 |
References | 29 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 2.3 [After extrusion] | 2.3 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | Initially 2.3 in diameter | 2.3 mm | Anonymous, 2006 Chapter 3 |
1 | Oocyte diameter | 2-2.7 [Oocyte ?] | 2.35 mm | Mack and Billard, 1984 |
2 | Egg size after water-hardening | 3-3.2 | 3.1 mm | Mellinger, 2002 |
2 | Egg size after water-hardening | 3.0-3.2 [After 24 hours in water] | 3.1 mm | Scott and Crossman, 1973 |
2 | Egg size after water-hardening | 2.8-3.0 | 2.9 mm | Sturn, 1994 |
2 | Egg size after water-hardening | Increase up to 3.2 mm after 24 hours in the water | 3.2 mm | Anonymous, 2006 Chapter 3 |
3 | Egg Buoyancy | Demersal | Demersal | Scott and Crossman, 1973 |
3 | Egg Buoyancy | Demersal [The eggs fall into crevices where they develop over the winter] | Demersal | Kerr and Grant, 1999 |
3 | Egg Buoyancy | The eggs of Salmonidae are buried in unguarded nests called 'redds' and are demersal-nonadheive | Demersal | Kunz, 2004 |
3 | Egg Buoyancy | Demersal eggs incubate on spawning substrate, often in crevices between and under rocks | Demersal | Goodyear et al, 1982 |
3 | Egg Buoyancy | Settle in rocky crevices where they remain | Demersal | Bradbury et al, 1999 |
4 | Egg adhesiveness | Not sticky [The eggs fall into crevices where they develop over the winter] | Non-Adhesive | Kerr and Grant, 1999 |
4 | Egg adhesiveness | The eggs of Salmonidae are buried in unguarded nests called 'redds' and are demersal-nonadheive | Non-Adhesive | Kunz, 2004 |
4 | Egg adhesiveness | Adhesive eggs | Adhesive | Bradbury et al, 1999 |
4 | Egg adhesiveness | Salmonidae, whose eggs are not sticky | Non-Adhesive | Woynarovich, 1962 |
5 | Incubation time | 140-150 days at 2.0-2.2°C | 145.0 days | Harris and Huslman, 2001 |
5 | Incubation time | 59 [7.8°C], 111.5 [4.0], 152.5 [2.0] | 59.0 days | Brooke, 1975 |
5 | Incubation time | 140 [0.5°C] | 140.0 days | Fishbase, 2006 |
5 | Incubation time | 150-170 | 160.0 days | Kerr and Grant, 1999 |
5 | Incubation time | 60.7 [5°C], 34.6 [7.5°C], 24.0 [10°C] and 18.2 [12.5°C] for 50% hatch | 60.7 days | Jensen, 1997 |
5 | Incubation time | About 140 days | 140.0 days | Anonymous, 2006 Chapter 3 |
5 | Incubation time | 4-6 months | 5.0 days | Bradbury et al, 1999 |
5 | Incubation time | Hatching occurred between 84 and 101 days (mean of 94) at an average temperature of 3.4°C (± 0.3°C) | 84.0 days | Brown and Taylor, 1992 |
6 | Temperature for incubation | 3-8 [Upper lethal incubation is 10°C, can be incubated successfully at 1°C ("cold breeding"), but such eggs have to be trasnfered to 5-10°C before hatching] | 5.5 °C | Rösch, 1995 |
6 | Temperature for incubation | 3.2-8.1 | 5.65 °C | Luczynski and Kirklewska, 1984 |
6 | Temperature for incubation | 2.0-2.2 | 2.1 °C | Harris and Huslman, 2001 |
6 | Temperature for incubation | 3.2-8 is the optimum range [The increased abnormalities at incubation temperatures of 0.5, 2.0 and 10.0] | 5.6 °C | Brooke, 1975 |
6 | Temperature for incubation | 6.5-9 | 7.75 °C | Rinchard et al, 2001 |
6 | Temperature for incubation | Normal development occurs over a temperature range of 0.5-6.1, with the optimum close to 0.5 [Eggs incubated at 10°C, suffer 99% mortality] | 3.3 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | Optimal temperature is 0.5-1.0°C [Variation tolerate 0.5-6.0] | 0.75 °C | Kerr and Grant, 1999 |
6 | Temperature for incubation | 4-8 | 6.0 °C | Czerkies, 2002 |
6 | Temperature for incubation | 3.4 ± 0.05 | 3.4 °C | Davis and Todd, 1998 |
6 | Temperature for incubation | About 43°F, 6.1°C | 43.0 °C | Goodyear et al, 1982 |
6 | Temperature for incubation | 5-12.5°C | 8.75 °C | Jensen, 1997 |
6 | Temperature for incubation | 0.6-6.1 is the optimal temperature | 3.35 °C | Anonymous, 2006 Chapter 3 |
6 | Temperature for incubation | 1-8°C | 4.5 °C | Bradbury et al, 1999 |
6 | Temperature for incubation | Mass hatching survival averaged 97.6% for average incubation temperatures ranging from 1.7°C to 6.4°C | 97.6 °C | Drouin et al, 1986 |
6 | Temperature for incubation | Incubated at an average temperature of 3.4°C (± 0.3°C) | 3.4 °C | Brown and Taylor, 1992 |
6 | Temperature for incubation | The best temperature seem to be 4°C | 4.0 °C | Mack and Billard, 1984 |
7 | Degree-days for incubation | About 300 | 300.0 °C * day | Harris and Huslman, 2001 |
7 | Degree-days for incubation | 300-400 | 350.0 °C * day | Brooke, 1975 |
7 | Degree-days for incubation | 227.4-303.3 [Between 0.5-12.5°C] | 265.35 °C * day | Jensen, 1997 |
7 | Degree-days for incubation | 320 [Hatching occurred between 84 and 101 days (mean of 94) at an average temperature of 3.4°C (± 0.3°C)] | 320.0 °C * day | Brown and Taylor, 1992 |
7 | Degree-days for incubation | 305 [2°C], 446 [4°C], 500 [5.9°C], 460 [7.8°C], 417 [10°C] | 305.0 °C * day | Mack and Billard, 1984 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 12.8 ± 0.4 | 12.8 mm | Harris and Huslman, 2001 |
8 | Initial larval size | 12.4-13.5 | 12.95 mm | Brooke, 1975 |
8 | Initial larval size | 10.8-11.5 | 11.15 mm | Sturn, 1994 |
8 | Initial larval size | 14.5 [Not trully specified if at hatching] | 14.5 mm | Davis and Todd, 1998 |
8 | Initial larval size | About 12 mm at 1 week | 12.0 mm | Anonymous, 2006 Chapter 3 |
8 | Initial larval size | 10.5-11.5 [At hatching, deduced from graph] | 11.0 mm | Taylor and Freeberg, 1984 |
8 | Initial larval size | 10.8-11.3 [Deduced from graph, at haching] | 11.05 mm | Brown and Taylor, 1992 |
8 | Initial larval size | 11.84 [After 231 days of incubation], 11.03 [After 183 days of incubation] and also 13.5 [At hatching] | 11.84 mm | Mack and Billard, 1984 |
9 | Larvae behaviour | Tend to remain in the spawning gravel | Demersal | Kerr and Grant, 1999 |
9 | Larvae behaviour | Rise to surface soon after hatching | Demersal | Goodyear et al, 1982 |
9 | Larvae behaviour | Young typically hatch from mid-May to mid-June and remain within the general vicinity of the spawning area | Demersal | Bradbury et al, 1999 |
9 | Larvae behaviour | After the third week, the larvae swam incessantly in tight formation in a circular motion from feeding station to feeding station. There, they congregated and swarmed around the point of entry of nauplii. Displaced larvae swam rapidly to the opposing feeding station where they strived aggressively to regain and advantageous feeding position. Between feedings the larvae continued swimming in tight schools near the surface. | Demersal | Drouin et al, 1986 |
9 | Larvae behaviour | Throughout the trial, larvae in all tanks formed a school only when startled but then soon disassociated | Demersal | Zitzow and Millard, 1988 |
10 | Reaction to light | React negatively to light | Photopositive | Kerr and Grant, 1999 |
11 | Temperature during larval development | 11-15 [Most suitable for growth and survival] | 13.0 °C | Rösch, 1995 |
11 | Temperature during larval development | 6.0-8.0 [During the initiation of feeding], then 14-15°C [Fourth to fifth week of rearing] | 7.0 °C | Harris and Huslman, 2001 |
11 | Temperature during larval development | Larvae most abundant in water of 4°C | 4.0 °C | Kerr and Grant, 1999 |
11 | Temperature during larval development | 10°C | 10.0 °C | Witokowski and Kokurewicz, 1981 |
11 | Temperature during larval development | Immediatly prior to egg hatching 100 eggs groupings were counted and placed in a series of 20 l aerated aquaria cooled to 12°C | 100.0 °C | Taylor and Freeberg, 1984 |
11 | Temperature during larval development | Trial 1: Rearing temperatures ranged from 11.0 to 13.5°C from days 1 to 20 and from 13.5 to 14.5°C from days 20 to 50. Trial 2: rearing temperatures ranged from 7.2 to 12.2°C from days 1 to 36 and from 12.2 to 17.2°C from days 36 to 50 | 1.0 °C | Zitzow and Millard, 1988 |
11 | Temperature during larval development | Reared at 6.9 ± 0.6°C | 6.9 °C | Brown and Taylor, 1992 |
12 | Sibling intracohort cannibalism | Never observed, no larval cannibalism was ever observed either in fish reared on artificial feed or on natural food | Absent | Kozlowski and Poczyczynski, 1999 |
13 | Full yolk-sac resorption | 150-160 [There were essentially no differences in survival among feeding regimes until day 15 [at 12°C], when yolk sac was complete and the larvae had to feed on exogeneous food resources.] | 155.0 °C * day | Taylor and Freeberg, 1984 |
13 | Full yolk-sac resorption | 150-170 [Yolk-sac absorption occurred between 23 and 25 days post-hatch (at 6.9°C). Yet, water temperatures in their this experiment were maintained at relatively low temperatures to simulate temperatures normally encountered in the Laurentian Great Lakes, while in early study was conducted at 12°C. At this higher temperature, larval lake whitefish exhausted energy reserves between 12 and 15 days post-hatch] | 160.0 °C * day | Brown and Taylor, 1992 |
14 | Onset of exogeneous feeding | In trial (at 11-13.5°C), lake whitefish were feeding in all tanks by day 3. In trial 2 (at 7.2-12.2°C), lake whitefish larvae were feeding in all tanks by day 3, but feed was not observed in the digestive tract until day 5 | 12.25 °C * day | Zitzow and Millard, 1988 |
14 | Onset of exogeneous feeding | Larvae were not fed until just prior to yolk sac absorption (21 after hatching) [Yet under natural conditions; larval lake whitefish are capable of feeding within 48 h after hatching | 21.0 °C * day | Brown and Taylor, 1992 |
14 | Onset of exogeneous feeding | Upon acclimatization to 10 and 5°C, a lethal temperature of 22.6°C and 20.6°C, respectively. | 10.0 °C * day | Jezierska et al, 1979 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | Reach at 2 [Not specified] | 2.0 year | Anonymous, 2006 Chapter 3 |
15 | Age at sexual maturity | In labrador, lake whitefish usually attain sexual maturiy in 5-11 years, although dwarf populations may mature as early as 2 years of age [Sex not specified] | 8.0 year | Bradbury et al, 1999 |
15 | Age at sexual maturity | Vary between 6 or 9 years for female | 6.0 year | Mack and Billard, 1984 |
16 | Length at sexual maturity | 23-27 [Sex mixed] | 25.0 cm | Fishbase, 2006 |
17 | Weight at sexual maturity | Vary between 0.29 to 0.600 depending on the area | 0.29 kg | Mack and Billard, 1984 |
18 | Female sexual dimorphism | Sexual dimoprhism is minimal | Absent | Willson, 1997 |
18 | Female sexual dimorphism | No change for female | Absent | Mack and Billard, 1984 |
19 | Relative fecundity | Estimated at 16.1 eggs per pound of fish | 16.1 thousand eggs/kg | Anonymous, 2006 Chapter 3 |
19 | Relative fecundity | 14.3 to 27.6 | 14.3 thousand eggs/kg | Mack and Billard, 1984 |
19 | Relative fecundity | The number of eggs per pound of fish bas been calculated to be 16100 for Lake Erie (possibly high since counting was done in Augts on "green" eggs), 9900 for Lake Ontario and 8200 for Lake Huron | 16100.0 thousand eggs/kg | Scott and Crossman, 1973 |
20 | Absolute fecundity | The equation describing the relationship between fecundity and fork length for these populations was : Fecundity=0.0404 length 3.527 (cm), e.g. vary between 20000 and 40000 for total length of 40 to 50 cm respectively | 0.04 thousand eggs | Healey and Nicol, 1975 |
22 | Onset of oogenesis | Initiated in early summer | ['July', 'August', 'September'] | Rinchard et al, 2001 |
23 | Intensifying oogenesis activity | Fall [Decreasing daylength triggers final maturation] | ['October', 'November', 'December'] | Rinchard et al, 2001 |
24 | Maximum GSI value | Female whitefish in Lake Erie habe been calculated to lose approximatively 11% of their weight at spawning | 11.0 percent | Scott and Crossman, 1973 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | Reach at 2 [Not specified] | 2.0 years | Anonymous, 2006 Chapter 3 |
27 | Age at sexual maturity | Males mature at an ealier age than females and die ealier | No data | Kerr and Grant, 1999 |
27 | Age at sexual maturity | In labrador, lake whitefish usually attain sexual maturiy in 5-11 years, although dwarf populations may mature as early as 2 years of age [Sex not specified] | 8.0 years | Bradbury et al, 1999 |
27 | Age at sexual maturity | Vary between 5 to 8 years [male] | 5.0 years | Mack and Billard, 1984 |
28 | Length at sexual maturity | 23-27 [Sex mixed] | 25.0 cm | Fishbase, 2006 |
29 | Weight at sexual maturity | Vary between 0.26 to 0.500 [Male] | 0.26 kg | Mack and Billard, 1984 |
30 | Male sexual dimorphism | Whitefish males commonly develop breeding tubercles, especially on the flanks, but tubercles are less well developped and rarer on females | Absent | Willson, 1997 |
30 | Male sexual dimorphism | Nuptial tubercles on the head | Present | Mack and Billard, 1984 |
31 | Onset of spermatogenesis | Initiated in early summer | ['July', 'August', 'September'] | Rinchard et al, 2001 |
32 | Main spermatogenesis activity | Fall [Decreasing daylength triggers final maturation] | ['October', 'November', 'December'] | Rinchard et al, 2001 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
37 | Spawning migration period | Migrate to spawning grounds around mid-October when water temperatures begin to drop | ['October'] | Kerr and Grant, 1999 |
37 | Spawning migration period | Move inshore to spawning grounds, migration begins in September-October, but occasionally as early as August; historically also ascend rivers to spawn | ['August', 'September', 'October'] | Goodyear et al, 1982 |
39 | Spawning season | Last 2 weeks of November | ['November'] | Harris and Huslman, 2001 |
39 | Spawning season | November [Mainly] and December | ['November', 'December'] | Rinchard et al, 2001 |
39 | Spawning season | November and December, but also from late September to October | ['September', 'October', 'November', 'December'] | Scott and Crossman, 1973 |
39 | Spawning season | November to December | ['November', 'December'] | Fishbase, 2006 |
39 | Spawning season | For the most part, spawning occurs in late October and early November [There have been instances where spawning has occurred into mid-December] | ['October', 'November', 'December'] | Kerr and Grant, 1999 |
39 | Spawning season | October-January, peak spawning usually occurs in late November-earlt December | ['January', 'October', 'November', 'December'] | Goodyear et al, 1982 |
39 | Spawning season | Spawn in the autumn, usually in November and December | ['October', 'November', 'December'] | Anonymous, 2006 Chapter 3 |
39 | Spawning season | In Labrador, spawning usually takes place in lakes in mid-September or October | ['September', 'October'] | Bradbury et al, 1999 |
39 | Spawning season | Some species of Coregonus in summer or winter | ['January', 'February', 'March', 'July', 'August', 'September'] | Willson, 1997 |
39 | Spawning season | From Ocotber to January, but usually from the end of October to the end of December | ['January', 'October', 'December'] | Mack and Billard, 1984 |
40 | Spawning period duration | Last for a week or ten days [Eggs being deposited over a period of several days] | No data | Kerr and Grant, 1999 |
40 | Spawning period duration | 2-5 weeks | 3.5 weeks | Goodyear et al, 1982 |
40 | Spawning period duration | The breeding season for an individual female does not probably last more than 10 days | 10.0 weeks | Mack and Billard, 1984 |
41 | Spawning temperature | Dropped below about 7.8 | 7.8 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | 4.4-10.0°C, even 3-4°C, most at less than 7-8°C [Most successful spawning occurs at temperatures <6.1°C] | 7.2 °C | Kerr and Grant, 1999 |
41 | Spawning temperature | About 53-33°F (i.e. 0.5-11.5°C), spawning at temperatures above 43°F (6°C) probably not successfull | 43.0 °C | Goodyear et al, 1982 |
41 | Spawning temperature | >8°C | 8.0 °C | Bradbury et al, 1999 |
42 | Spawning water type | Spawning shoals of lakes | Stagnant water | Kerr and Grant, 1999 |
42 | Spawning water type | Inshore areas, bays, ledges, shoals, reefs, often same sites used by lake trout | Stagnant water | Goodyear et al, 1982 |
42 | Spawning water type | Unlike many other species, flowing water is not required for spawning | Flowing or turbulent water | Bradbury et al, 1999 |
42 | Spawning water type | Lakes, streams | Stagnant water | Willson, 1997 |
43 | Spawning depth | Shallow waters at depth of less than 7.6 m | 7.6 m | Scott and Crossman, 1973 |
43 | Spawning depth | Spawn at depths between 1.8-18.3 m [Either at 9 m , 6-14 m deep, or 7.6 m ] | 10.05 m | Kerr and Grant, 1999 |
43 | Spawning depth | Several inches-100 feet, but usually less than 30 feet; often spawn in shallower portions of same reefs used by lake trout | 100.0 m | Goodyear et al, 1982 |
43 | Spawning depth | Shallow water at depth of less than 7.6 m | 7.6 m | Anonymous, 2006 Chapter 3 |
43 | Spawning depth | Spawning in small lakes occurs most frequently at depths <5m, while it may occur uo to 30 m in larger lakes | 30.0 m | Bradbury et al, 1999 |
43 | Spawning depth | Usually 2-4 m deep, or less than 5 m | 3.0 m | Mack and Billard, 1984 |
44 | Spawning substrate | Hard or stoney bottom but sometimes over sand | Lithophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Bottom type is often flat rock, stone or gravel or sometimes sand [Spawning shoals could also be composed of cobble-boulder limestone over a sand, clay or bedrock base located from the shoreline out to a depth of several metres] | Lithophils | Kerr and Grant, 1999 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Over hard, clean bottom, including stone, rubble, honeycombed rock, gravel, sand, and clay; used a variety of substrate types than lake trout; vegetation suaully not present; but spawning over "moss" has been reported | Lithophils | Goodyear et al, 1982 |
44 | Spawning substrate | Over rocky, hard, or sandt susbtrate | Lithophils | Anonymous, 2006 Chapter 3 |
44 | Spawning substrate | Preferred spawning susbrate appears to be gravel, cobble or boulder, but spawning may occasionally occur over sand [Mud botoms are generally avoided by both river and lake spawners] | Lithophils | Bradbury et al, 1999 |
44 | Spawning substrate | Pebbles or big rocks | Lithophils | Mack and Billard, 1984 |
45 | Spawning site preparation | Eggs are deposited more or less randomly over the spanwing grounds by the parents | Susbtrate chooser | Scott and Crossman, 1973 |
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 | Balon, 1975 |
45 | Spawning site preparation | Eggs are broadcast near surface | Open water/substratum scatter | Goodyear et al, 1982 |
45 | Spawning site preparation | Eggs are brodcast into the water column | No category | Bradbury et al, 1999 |
46 | Nycthemeral period of oviposition | Spawning fish are active and may jump and thrash about, especially at night | Night | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | Spawning occurs at night | Night | Fishbase, 2006 |
46 | Nycthemeral period of oviposition | Spawning activity occurs at night | Night | Kerr and Grant, 1999 |
46 | Nycthemeral period of oviposition | Probably at night | Night | Mack and Billard, 1984 |
47 | Mating system | A female and one or more males rise to the surface, release eggs and milt and descend separately toward the bottom | No category | Fishbase, 2006 |
48 | Spawning release | Eggs being deposited over a period of several days | Multiple | Kerr and Grant, 1999 |
49 | Parity | Breeds annually in the southern parts of the range, but only every other year or even third year in the arctic and sib-arctic region | No category | Fishbase, 2006 |
49 | Parity | Lake withefish have a maximum life spawn of about 18 years | No category | Kerr and Grant, 1999 |
49 | Parity | Return to deep water occurs soon after spawning | Iteroparous | Goodyear et al, 1982 |
49 | Parity | After spawning, adullts return to deeper water | Iteroparous | Bradbury et al, 1999 |
49 | Parity | Typically iteroparous, although reproduction does not occur every year for some individuals and populations | Iteroparous | Willson, 1997 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |
50 | Parental care | No parental care is provided to the eggs or young | No care | Kerr and Grant, 1999 |
50 | Parental care | After spawning, adullts return to deeper water | No care | Bradbury et al, 1999 |
50 | Parental care | Parental care is absent in coregonids and lake char | No care | Willson, 1997 |