Trait completeness | 68% |
Total data | 133 |
References | 29 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 4.5-6 | 5.25 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 5-6 [Not specified] | 5.5 mm | Perrin, 2001 |
1 | Oocyte diameter | 5-6 | 5.5 mm | Fishbase, 2006 |
1 | Oocyte diameter | 5-6 [In ovary, at maturity] | 5.5 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 5-6 [Not specified, but seems unswollen] | 5.5 mm | Mittelbach and Persson, 1998 |
1 | Oocyte diameter | 5.5 [Mean diameter of mature, fully yolked, ovarian oocyte] | 5.5 mm | Olden et al, 2006 |
2 | Egg size after water-hardening | 5.7 ± 0.2 [Fertilized eggs] | 5.7 mm | Beauchamp et al, 1992 |
2 | Egg size after water-hardening | 3.7-6.8, with a mean of 5.0 [Size of ripe egg] | 5.25 mm | Groot, 1996 |
2 | Egg size after water-hardening | 5.4 [Fully hardened eggs] | 5.4 mm | Penaz, 1981 |
3 | Egg Buoyancy | Demersal (on the bottom) | Demersal | Fishbase, 2006 |
3 | Egg Buoyancy | Demersal [Fertilized egg fall into the crevices between the large rocks] | Demersal | Scott and Crossman, 1973 |
3 | Egg Buoyancy | The eggs of Salmonidae are buried in unguarded nests called 'redds' and are demersal-nonadheive | Demersal | Kunz, 2004 |
3 | Egg Buoyancy | Shortly after release, eggs settle to the bottomand lodge in crevices among rocks | Demersal | Bradbury et al, 1999 |
3 | Egg Buoyancy | Eggs usually incubate in crevices in the susbtrate | Demersal | Goodyear et al, 1982 |
4 | Egg adhesiveness | Fertilized eggs fall into crevices of the spawning substrate | 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 | Salmonidae, whose eggs are not sticky | Non-Adhesive | Woynarovich, 1962 |
5 | Incubation time | 105-147 | 126.0 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 105-147 [15-21 weeks] | 126.0 days | Perrin, 2001 |
5 | Incubation time | 15-21 weeks, hatching normally occurs between mid-February and late March | 18.0 days | Fishbase, 2006 |
5 | Incubation time | 105-147 [15-21 weeks at 0.3-1°C] | 126.0 days | Scott and Crossman, 1973 |
5 | Incubation time | Normally hatch in about 50 days at 10°C [15 to 21 weeks at temperatures between 0.1-10°C] | 5.05 days | Kerr and Grant, 1999 |
5 | Incubation time | 150.0 [Mean time to egg hatch within the range of average post-spawning water temperatures] | 150.0 days | Olden et al, 2006 |
5 | Incubation time | Incubate for 4-5 months over winter | 4.5 days | Bradbury et al, 1999 |
5 | Incubation time | Initial hatch after 70 days and 90% hatch after 81 days at 7°C and 49 days and 56 days at 10°C respectively | 70.0 days | Carlson and Siebert, 1974 |
5 | Incubation time | 162.3 [1.83°C], 86.3 [5.1°C], 80.5 [6.72°C], and 49 [10°C] | 162.3 days | Embody, 1934 |
5 | Incubation time | Eggs hatch in 2-5 months at 47-35°F, in late January-May | 3.5 days | Goodyear et al, 1982 |
6 | Temperature for incubation | 0.3-1 in normal conditions | 0.65 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 5-9 during incubation period | 7.0 °C | Beauchamp et al, 1992 |
6 | Temperature for incubation | < 10°C for optimal egg incubation | 10.0 °C | Kerr and Grant, 1999 |
6 | Temperature for incubation | Separate lots of eggs were reared at different temperatures: 0.5-6°C | 3.25 °C | Gunn and Noakes, 1987 |
6 | Temperature for incubation | Test temperatures were 7 and 10°C within the optimum range and near the higher limit for incubation | 7.0 °C | Carlson and Siebert, 1974 |
6 | Temperature for incubation | Could be incubated at 1.8°C | 1.8 °C | Babiak and Dabrowski, 2003 |
7 | Degree-days for incubation | 500 | 500.0 °C * day | Perrin, 2001 |
7 | Degree-days for incubation | 440 | 440.0 °C * day | Pennel and Barrington. 1996 (79) |
7 | Degree-days for incubation | 490 | 490.0 °C * day | Bascinar and Okumus, 2004 |
7 | Degree-days for incubation | Hatching occurred several weeks before the experiments at about 450-500 DD | 475.0 °C * day | Gunn and Noakes, 1987 |
7 | Degree-days for incubation | About 500-550 [Initial hatch after 70 days and 90% hatch after 81 days at 7°C and 49 and 56 at 10°C respectively] | 525.0 °C * day | Carlson and Siebert, 1974 |
2 | Egg size after water-hardening | 5.10 | 5.1 mm | Shuter et al, 2005 |
5 | Incubation time | 105-147 | 126.0 days | Martin, 1957 |
7 | Degree-days for incubation | 0.28-1; 105-147 | 80.64 °C * day | Martin, 1957 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 16 | 16.0 mm | Mittelbach and Persson, 1998 |
8 | Initial larval size | 15.2 | 15.2 mm | Kerr and Grant, 1999 |
8 | Initial larval size | 16.1 | 16.1 mm | Olden et al, 2006 |
9 | Larvae behaviour | Fry remain on the spawing shoals about a month or so after hatching while the yolk sac is being absorbed | Demersal | Kerr and Grant, 1999 |
9 | Larvae behaviour | Upon hatching alevins remain near the bottom in spawning areas for several weeks to three months before moving to deeper water | Demersal | Bradbury et al, 1999 |
9 | Larvae behaviour | Remain in crevices in susbrate for about 1 month | Demersal | Goodyear et al, 1982 |
11 | Temperature during larval development | 10.8°C preferred by fingerlings [11.7°C preferred for yearlings] | 10.8 °C | Kerr and Grant, 1999 |
11 | Temperature during larval development | Reared at 4.9 ± 0.1°C | 4.9 °C | Gunn and Noakes, 1987 |
14 | Onset of exogeneous feeding | About 140 [Initial feeding started at 101 days after fertilization and 90% hatch occurred at 81 days at 7°C and 60 days after fertilization and 90% hatch at 10°C, i.e. 20 days at 7°C and 14 days at 10°C] | 140.0 °C * day | Carlson and Siebert, 1974 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 6-7 | 6.5 year | Pennel and Barrington. 1996 (77) |
15 | Age at sexual maturity | 6-7 [Sex not specified] | 6.5 year | Billard, 1997 |
15 | Age at sexual maturity | 6-7 [Not specified] | 6.5 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | Mostly between 4 to 13 | 4.0 year | Kerr and Grant, 1999 |
15 | Age at sexual maturity | 5.0 [Both sex] | 5.0 year | Olden et al, 2006 |
15 | Age at sexual maturity | In Labrador, lake trout usually attain sexual maturity in 6-11 years [Not specified] | 8.5 year | Bradbury et al, 1999 |
16 | Length at sexual maturity | 38.0 [Both sex] | 38.0 cm | Olden et al, 2006 |
19 | Relative fecundity | 0.8-2.4 | 1.6 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | 2-16 | 9.0 thousand eggs/kg | Perrin, 2001 |
19 | Relative fecundity | 0.9-2.6 | 1.75 thousand eggs/kg | Mittelbach and Persson, 1998 |
19 | Relative fecundity | The number of eggs deposited depends on the size of the female but ranges from 400-1200 eggs per pound of female | 800.0 thousand eggs/kg | Scott and Crossman, 1973 |
20 | Absolute fecundity | A 32-inch (813 mm) female from the Great Lakes may deposit up to 18,000 eggs | 32.0 thousand eggs | Scott and Crossman, 1973 |
24 | Maximum GSI value | Mean of 14.6 (range 12.3-17.6%) for different populations | 14.95 percent | Fleming, 1998 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 6-7 [Sex not specified] | 6.5 years | Billard, 1997 |
27 | Age at sexual maturity | 6-7 [Not specified] | 6.5 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | Mostly between 4 to 13 [Both sex], river spawning male trout were found to mature aty 7 [In most cases, males mature over a year earlier than females] | 4.0 years | Kerr and Grant, 1999 |
27 | Age at sexual maturity | 5.0 [Both sex] | 5.0 years | Olden et al, 2006 |
27 | Age at sexual maturity | In Labrador, lake trout usually attain sexual maturity in 6-11 years [Not specified] | 8.5 years | Bradbury et al, 1999 |
28 | Length at sexual maturity | 38.0 [Both sex] | 38.0 cm | Olden et al, 2006 |
30 | Male sexual dimorphism | Male lake char are capable of developing a kype, but they almost never do. Male lake char may be more iridescent than females, sport a black lateral stripe, or develop (in soem populations) breeding tubercles, but generally they show less sexual dimoprhism than other char do [In Salmo, most Salvelinus, and most Oncorhynchus, a major sexual difference is found in the development , in normal breeding individuals, of elongated, hooked jaws with enlarged teeth. An upturned lower jaw is technically called a kype; an enlarged and often distorted upper jaw is termed a snout. Kype and sount development differs not only among individuals but also among species and conspecific populations: it is generally greater in stream-dwelling and anadromous forms than in lake-spawning or strickly freshwater forms.Kypes and snouts are best developed in males, although females of some species also develop smaller ones. Another secondarytrait is a hump anterior to dorsal fin, found especially in males.] | Present | Willson, 1997 |
30 | Male sexual dimorphism | Breeding tubercles present | Present | Kratt and Smith, 1978 |
30 | Male sexual dimorphism | Males are bigger than females | Absent | Fleming, 1998 |
33 | Maximum GSI value | Mean of 3.1 for different population | 3.1 percent | Fleming, 1998 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
37 | Spawning migration period | Move from deep water to spawning grounds in shallower water on offshore reefs, in littoral waters, or in tributaries. Movement usually begins in late August or September; fish arrive on grounds 1-2 weeks before spawning begins | ['August', 'September'] | Goodyear et al, 1982 |
38 | Homing | In certain lakes, he returns to natal spawning grounds | Present | Perrin, 2001 |
38 | Homing | Evidence of homing | Present | Scott and Crossman, 1973 |
39 | Spawning season | October-November | ['October', 'November'] | Billard, 1997 |
39 | Spawning season | September to November or during winter | ['January', 'February', 'March', 'September', 'October', 'November'] | Bruslé and Quignard, 2001 |
39 | Spawning season | November-December, but also August-September and until January | ['January', 'August', 'September', 'November', 'December'] | Fishbase, 2006 |
39 | Spawning season | Mainly occurs in October, sometimes as early as September in the north or as late as November in south | ['September', 'October', 'November'] | Scott and Crossman, 1973 |
39 | Spawning season | October-November | ['October', 'November'] | Beauchamp et al, 1992 |
39 | Spawning season | Primarily fall spaweners although reprodcution is know to occur as early as June in Lake Superioir and as late as January in Lake Tahoe, Nevada | ['January', 'June', 'October', 'November', 'December'] | Kerr and Grant, 1999 |
39 | Spawning season | On most areas of Canada, spawning occurs in late summer-early fall, mainly in September or October in Labrador. Several investigators have suggested that declining water temperatures and photoperiod coupled with stron on-shore winds are necessary factors triggering spawning | ['July', 'August', 'September', 'October', 'November', 'December'] | Bradbury et al, 1999 |
39 | Spawning season | Salmo and most char are fall breeders, although a few populations of Arctic char breed in spring | ['April', 'May', 'June', 'October', 'November', 'December'] | Willson, 1997 |
39 | Spawning season | Most spawning occurs in October and November when temperature is falling from 58 to 37°F; however some races may begin spawning in June | ['June', 'October', 'November', 'December'] | Goodyear et al, 1982 |
40 | Spawning period duration | The spawning period generally lasts between seven to 18 days, and lake trout spawning in Algouquin Park lakes often occurs during the latter portion of October and lasts for 10 days | 18.0 weeks | Kerr and Grant, 1999 |
41 | Spawning temperature | 4.5-14 | 9.25 °C | Pennel and Barrington. 1996 (79) |
41 | Spawning temperature | < 10 | 10.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | Starts when temperature below 10°C | 10.0 °C | Perrin, 2001 |
41 | Spawning temperature | From 8-9 to 10.6-13.9°C | 8.5 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | 8-11 | 9.5 °C | Mittelbach and Persson, 1998 |
41 | Spawning temperature | 9-13 [Onset of spawning appears to be stimulated by heavy winds when water temperatures drop to near 10°C, Increase and prolonged cloud cover can also advance the spawning period] | 11.0 °C | Kerr and Grant, 1999 |
41 | Spawning temperature | 8 [Temperature at which spawning is typically initiated] | 8.0 °C | Olden et al, 2006 |
42 | Spawning water type | Inland lakes, rarely in rivers | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Mounds | No category | Beauchamp et al, 1992 |
42 | Spawning water type | Spawn in shallow inshore areas of lakes, rarely in streams [Spawning areas are often exposed to prevaling winds that wave action and water currents keep the area free of sand, silt and detritus] | Stagnant water | Bradbury et al, 1999 |
42 | Spawning water type | Lakes, streams | Stagnant water | Willson, 1997 |
42 | Spawning water type | Areas with current, including shorelines, reefs, shoals, ledges, bars, channels, bays, river mouths, and rivers | Stagnant water | Goodyear et al, 1982 |
43 | Spawning depth | Depth of less than 12.2, and sometimes as shallow as 30 cm | 12.2 m | Scott and Crossman, 1973 |
43 | Spawning depth | Deep water (40-60 m ) over beds of macrophytes [Only one report] | 50.0 m | Beauchamp et al, 1992 |
43 | Spawning depth | Lake trout spawn at a great variety of depths, less than 36.6 m [Most inland lake spawning shoals are less than six meters deep, also observed between 15 cm to 3.7 m deep] Some population choose to spawn over deep-water mounds (40-60 m) covered with beds of Clara delicauta | 50.0 m | Kerr and Grant, 1999 |
43 | Spawning depth | Spawn over a variety of depths rangin from 0.5-55m, or greater than 100 m. In larger lakes, psanwing typically occurs at depths between 5 and 10 m, while in smaller lakes spawning has been reported to occur at depths between 0.1-5 m | 2.55 m | Bradbury et al, 1999 |
43 | Spawning depth | Few inches - 600 feet, depending on race of Lake trout; planted varieties usually at depths less than 30 feet | 600.0 m | Goodyear et al, 1982 |
44 | Spawning substrate | Gravels | Lithophils | Perrin, 2001 |
44 | Spawning substrate | Most often occurs over a large boulder or rubble bottom | No category | Scott and Crossman, 1973 |
44 | Spawning substrate | Mostly over cobble, boulder and borken rock substrates, only once on macrophytes | Lithophils | Beauchamp et al, 1992 |
44 | Spawning substrate | Lake trout ave very selective in their choice of sites for spawning: good spawning substrate consists of clean cobble, boulder or broken angular rock with large interstices that provide protection to eggs [Prefereed spawinng grounds consist of largest diameter rock rock with three to 15 cm and is common,ly interspersed with larger boulders, average diameter of 4.3] | Lithophils | Kerr and Grant, 1999 |
44 | Spawning substrate | Lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | The spawning substrate is usually composed of large gravel (>2 cm in diameter), cobble and rubble interspered with boulders and is generally free of sand, mud, detritus and vegetation. | Lithophils | Bradbury et al, 1999 |
44 | Spawning substrate | The spawning rubble, consisting of broken, mixed pieces (about 10-30 cm length) of quarzite, feldspar, and granite, is underlain with solid bedrock | Lithophils | Gunn and Keller, 1984 |
44 | Spawning substrate | Eggs are broadcast by shallow-water races over rough, silt-free bottom, including honeycomb rock, rubble, boulders, and gravel; deep-water races spawn over clay, sand, mud, and silt; planter varieties spawn over all substrates | Lithophils | Goodyear et al, 1982 |
45 | Spawning site preparation | Open water / substratum egg scatterers [Males reach spawning beds first and spend some time cleaning the rocks] | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Cleaning of the spawning grounds consisted of brushing the rocks with body or tail fin, or rubbing then with the snout | No category | Scott and Crossman, 1973 |
45 | Spawning site preparation | The males appear to clean the rocks with her tails but do not build a nest | No category | Kerr and Grant, 1999 |
45 | Spawning site preparation | Brood hiders | Susbtrate chooser | Balon, 1975 |
45 | Spawning site preparation | No nest | Open water/substratum scatter | Fleming, 1998 |
46 | Nycthemeral period of oviposition | The spawning act occurs mostly at night, with peak spawning between dusk and 9 or 10 pm | Night | Fishbase, 2006 |
46 | Nycthemeral period of oviposition | Spawning occur in the night, mostly from 19-22 | Night | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | Most spawning takes place during the hours of darkness between dusk and 2300 hours | Dusk | Kerr and Grant, 1999 |
47 | Mating system | By pair, on occassion as many as seven males and three females may engage in a mass spawning act | Monogamy | Fishbase, 2006 |
47 | Mating system | One or two males may spawn with one female, or a group of males and females may spawn together, extruding eggs and sperm over rocky bottom | Promiscuity | Scott and Crossman, 1973 |
47 | Mating system | A male will court many females within its range [Lake trout visit and probably spawn on more than one shoal] | Polygyny | Kerr and Grant, 1999 |
47 | Mating system | Disperse to deeper water several weeks after spawning | No category | Goodyear et al, 1982 |
48 | Spawning release | Batch spawner, the spawning act (one female and one or two males) is repeated until the female releases all her eggs | Multiple | Fishbase, 2006 |
49 | Parity | Spawning occurs annually in southern areas, every other year in other parts | No category | Fishbase, 2006 |
49 | Parity | Can live to 40 years of age | No category | Kerr and Grant, 1999 |
49 | Parity | Dispersal of adults from spawning areas begins shortly after spawning | No category | Bradbury et al, 1999 |
49 | Parity | Lake char females commonly breed in alternate years, especially in the north. These fish are potentially long lived (>25 years), and indiduals may reproduce many times if maturity is not delayed | No category | Willson, 1997 |
49 | Parity | Mean of 53 (range 6-79%) of repeat spawners in different populations | No category | Fleming, 1998 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |
50 | Parental care | Dispersal of adults from spawning areas begins shortly after spawning | No care | Bradbury et al, 1999 |
50 | Parental care | Parental care is absent in coregonids and lake char | No care | Willson, 1997 |
50 | Parental care | No defence | No care | Fleming, 1998 |