Trait completeness | 82% |
Total data | 222 |
References | 35 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 3.5-4 | 3.75 mm | Mellinger, 2002 |
1 | Oocyte diameter | 3.3-4 | 3.65 mm | Internet, 2005 |
1 | Oocyte diameter | 3.5-4.0 [Before they are laid] | 3.75 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 3.5-4.0 [Not specified, but seems unswollen] | 3.75 mm | Mittelbach and Persson, 1998 |
1 | Oocyte diameter | 3-4 | 3.5 mm | Anonymous, 2006 Chapter 3 |
1 | Oocyte diameter | 3.8 [Mean diameter of mature, fully yolked, ovarian oocyte] | 3.8 mm | Olden et al, 2006 |
1 | Oocyte diameter | The diameter of the eggs fixed just after spawning, with the chorion removed, averaged 3.2 mm | 3.2 mm | Riggs, 1961 |
1 | Oocyte diameter | 3 [Ovocyte] | 3.0 mm | Legendre et al, 1997 |
1 | Oocyte diameter | Mean of 2.356 ± 0.049 [Oocyte diameter in May] | 2.36 mm | Pacoli et al, 1990 |
1 | Oocyte diameter | Egg diameter (frozen) => 2.2 ± 01. (4FO control), 2.4 ± 0.2 (4PF), 2.2 ± 0.1 (10FO), 2.3 ± 0.1 (10PF) | 2.2 mm | Sink and Lochman, 2008 |
2 | Egg size after water-hardening | 3.9 [The diameter of the egg membrane after activation] | 3.9 mm | Makeeva and Emel'yanova, 1993 |
2 | Egg size after water-hardening | The fertilized egg are about 3.5 but range up to 5.1 | 3.5 mm | Grizzle, 1985 |
2 | Egg size after water-hardening | 3.5 [Fertilized swollen egg] | 3.5 mm | Legendre et al, 1997 |
2 | Egg size after water-hardening | 3.5 [Egg size] | 3.5 mm | Hecht, 1996 |
2 | Egg size after water-hardening | Egg production by individual females was considered successful if eggs appeared normal ( yellow and ~ 5 mm in diameter) | 5.0 mm | Lang and Tiersch, 2007 |
3 | Egg Buoyancy | Demersal | Demersal | Internet, 2005 |
3 | Egg Buoyancy | Settle to the bottom | Demersal | Wellborn and Tucker, 1985 |
3 | Egg Buoyancy | Demersal eggs lay in the nest | Demersal | Rue, 2001 |
3 | Egg Buoyancy | Incubates on bottom of nest | Demersal | Goodyear et al. et al, 1982 |
3 | Egg Buoyancy | Demersal | Demersal | Kunz, 2004 |
3 | Egg Buoyancy | Demersal | Demersal | Riggs, 1961 |
3 | Egg Buoyancy | Most catfish possess demersal eggs | Demersal | Legendre et al, 1997 |
4 | Egg adhesiveness | Very adhesive | Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Highly viscous and they stick together | Adhesive | Makeeva and Emel'yanova, 1993 |
4 | Egg adhesiveness | Fertilized egg are adhesive and form an egg mass | Adhesive | Grizzle, 1985 |
4 | Egg adhesiveness | Within a minute they become sticky and adhere to each other and the aquarium bottom | Adhesive | Wellborn and Tucker, 1985 |
4 | Egg adhesiveness | Mass of adhesive eggs | Adhesive | Goodyear et al. et al, 1982 |
4 | Egg adhesiveness | Adhesive | Adhesive | Kunz, 2004 |
4 | Egg adhesiveness | Eggs of channel catfish are demersal and adhesive. They adhere to each other in large masses, usually forming a single mass per spawn | Adhesive | Riggs, 1961 |
4 | Egg adhesiveness | Eggs adhere together | Adhesive | Legendre et al, 1997 |
4 | Egg adhesiveness | Formed a cohesive mass following activation | Non-Adhesive | Lang and Tiersch, 2007 |
5 | Incubation time | 7-10 [At 24-26°C], 6 [At 24°C] | 8.5 days | Internet, 2005 |
5 | Incubation time | 4.5 [At 28-29°C], 5 [26-28°C] | 28.5 days | Makeeva and Emel'yanova, 1993 |
5 | Incubation time | 5-10 days [15.6-27.8] | 7.5 days | Scott and Crossman, 1973 |
5 | Incubation time | 5-10 days | 7.5 days | Grizzle, 1985 |
5 | Incubation time | 6-7 [27°C], 9-10 [15.6-18.4°C]; 5-10 [15.6-27.8°], eggs will not develop below 15.5°C and develop best at 27°C | 6.5 days | Kerr and Grant, 1999 |
5 | Incubation time | 5-10 | 7.5 days | Rue, 2001 |
5 | Incubation time | Hatch in 5 days at 72-82°F and in 10 days at 60°F | 77.0 days | Goodyear et al. et al, 1982 |
5 | Incubation time | 7-10 | 8.5 days | Anonymous, 2006 Chapter 3 |
5 | Incubation time | 6.0 [Mean time to egg hatch within the range of average post-spawning the range post-spawning water temperatures] | 6.0 days | Olden et al, 2006 |
5 | Incubation time | 5-8 at 25-28°C | 6.5 days | Legendre et al, 1997 |
5 | Incubation time | 5 | 5.0 days | Hecht, 1996 |
6 | Temperature for incubation | 24-26 | 25.0 °C | Internet, 2005 |
6 | Temperature for incubation | 15.6-27.8 | 21.7 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | At 30°C or higher, water temperature can adversely affect egg developmet and fry survival | 30.0 °C | Wellborn and Tucker, 1985 |
6 | Temperature for incubation | Incubated at 24.7-26.8°C | 25.75 °C | Riggs, 1961 |
6 | Temperature for incubation | 25-28 [Water temperatures of 30°C or higher can adversely affect egg development and fry survival | 26.5 °C | Legendre et al, 1997 |
6 | Temperature for incubation | The eggs collected on June 19 were held in 17°C water to slow egg development […] The mean water temperature was 28°C (ranged from 26 to 29°C) | 19.0 °C | Rach et al, 2004 |
6 | Temperature for incubation | Well water (24.4-25.5°C) was supplied to the incubator at approximately 12 L min-1 | 24.95 °C | Sink and Lochman, 2008 |
6 | Temperature for incubation | Days-post egg mass collection from spawning tanks => 4.4 ± 0.4 (diet 4FO, control), 4.8 ± 0.3 (4PF), 4.9 ± 0.3 (10FO), 4.3 ± 0.3 (10 PF) [at 24.4-25.5°C] | 4.4 °C | Sink and Lochman, 2008 |
6 | Temperature for incubation | Water at a temperature of 23-24°C | 23.5 °C | Brzuska and Adamek, 1999 |
7 | Degree-days for incubation | About 150 | 150.0 °C * day | Internet, 2005 |
7 | Degree-days for incubation | 130-140 | 135.0 °C * day | Makeeva and Emel'yanova, 1993 |
7 | Degree-days for incubation | 140-150 | 145.0 °C * day | Scott and Crossman, 1973 |
2 | Egg size after water-hardening | 3.50-4.00 | 3.75 mm | Scott and Crossman, 1998 |
7 | Degree-days for incubation | 15.6-27.8; 5-10 | 162.75 °C * day | Scott and Crossman, 1998 |
2 | Egg size after water-hardening | 3.51-3.87 | 3.69 mm | Quintero et al, 2011 |
2 | Egg size after water-hardening | 3.15-3.75 | 3.45 mm | Quintero et al, 2011 |
2 | Egg size after water-hardening | 3.40-3.92 | 3.66 mm | Quintero et al, 2011 |
2 | Egg size after water-hardening | 3.48-3.94 | 3.71 mm | Quintero et al, 2011 |
5 | Incubation time | 3-8 | 5.5 days | Riehl and Baensch, 1991 |
7 | Degree-days for incubation | 18.3; 14.9 | 272.67 °C * day | Small, 2006 |
7 | Degree-days for incubation | 21.15; 10 | 211.5 °C * day | Small, 2006 |
7 | Degree-days for incubation | 23.9; 7.16 | 171.12 °C * day | Small, 2006 |
7 | Degree-days for incubation | 26.7; 5.48 | 146.32 °C * day | Small, 2006 |
7 | Degree-days for incubation | 29.5; 4.54 | 133.93 °C * day | Small, 2006 |
7 | Degree-days for incubation | 32.2; 4.09 | 131.7 °C * day | Small, 2006 |
7 | Degree-days for incubation | 15.99; 21.51 | 343.94 °C * day | Small and Bates, 2001 |
7 | Degree-days for incubation | 21.02; 9.63 | 202.42 °C * day | Small and Bates, 2001 |
7 | Degree-days for incubation | 26.04; 6.14 | 159.89 °C * day | Small and Bates, 2001 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 6.4 | 6.4 mm | Internet, 2005 |
8 | Initial larval size | 7-7.5 | 7.25 mm | Makeeva and Emel'yanova, 1993 |
8 | Initial larval size | 6 | 6.0 mm | Mittelbach and Persson, 1998 |
8 | Initial larval size | 6.4 | 6.4 mm | Anonymous, 2006 Chapter 3 |
8 | Initial larval size | 8.4 | 8.4 mm | Olden et al, 2006 |
9 | Larvae behaviour | Stay at or near the nest for several days then disperse into shallow water | Demersal | Internet, 2005 |
9 | Larvae behaviour | All prelarvae are in contact with one another | Demersal | Makeeva and Emel'yanova, 1993 |
9 | Larvae behaviour | Newly hatched fish have large yolks and remain on the bottom for 2-5 days and then swim to the surface adn begin to feed | Demersal | Scott and Crossman, 1973 |
9 | Larvae behaviour | Newly hatched larvae fish remain on bottom for 2-5 days then swim to surface and begin to feed | Demersal | Kerr and Grant, 1999 |
9 | Larvae behaviour | Remain in the nest up to 8 days | Demersal | Goodyear et al. et al, 1982 |
9 | Larvae behaviour | Remain near the nest for a few days than disperse to shallow water | Demersal | Anonymous, 2006 Chapter 3 |
10 | Reaction to light | The prelarvae avoid bright light and are indifferent to diffuse light [The larvae are strongly negatively phototaxic and remain in a group in the darkest places or hide under stones] | Photophobic | Makeeva and Emel'yanova, 1993 |
11 | Temperature during larval development | 27-28 | 27.5 °C | Makeeva and Emel'yanova, 1993 |
11 | Temperature during larval development | Water temperatures of 30°C or higher can adversely affect egg development and fry survival | 30.0 °C | Legendre et al, 1997 |
11 | Temperature during larval development | For most Siluroidei species it would appear that a temperature range between 26 and 30°C is optimal for larval and early juvenile rearing | 26.0 °C | Hecht, 1996 |
11 | Temperature during larval development | The average temperature during the experiment was 21.6 ± 1.0°C | 21.6 °C | El-Saidy et al, 2000 |
11 | Temperature during larval development | Ranges for water temperatures during trial 1 were: 23-32°C | 27.5 °C | Weirich et al, 2001 |
13 | Full yolk-sac resorption | 448 | 448.0 °C * day | Makeeva and Emel'yanova, 1993 |
13 | Full yolk-sac resorption | 5-16 days after hatching, young have exhausted the yolk | 10.5 °C * day | Grizzle, 1985 |
13 | Full yolk-sac resorption | 5-10 days | 7.5 °C * day | Hecht, 1996 |
14 | Onset of exogeneous feeding | 700 | 700.0 °C * day | Makeeva and Emel'yanova, 1993 |
14 | Onset of exogeneous feeding | Yolk absorption, feeding activity, and swimming of fry at the surface normally occurs at 4-5 d after hatching (fry at this stage are commonly referred to as "swim-up" fry [23-33°C] | 4.5 °C * day | Weirich et al, 2001 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 5-8 [Not specified] | 6.5 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | 5-8 [Not specified] | 6.5 year | Anonymous, 2006 Chapter 3 |
15 | Age at sexual maturity | 2.0 [Both sex] | 2.0 year | Olden et al, 2006 |
15 | Age at sexual maturity | Can mature as early as 2 years, but broodfish of at least 3 years are preferred | 2.0 year | Legendre et al, 1997 |
16 | Length at sexual maturity | 36 [Unsexed] | 36.0 cm | Fishbase, 2006 |
16 | Length at sexual maturity | 26.7-40.6 [Both sex] | 33.65 cm | Scott and Crossman, 1973 |
16 | Length at sexual maturity | 27.5 [Both sex] | 27.5 cm | Olden et al, 2006 |
17 | Weight at sexual maturity | Can mature as early as 0.34 kg , but broodfish of at least 1.5 kg are preferred sex not specified] | 0.34 kg | Legendre et al, 1997 |
18 | Female sexual dimorphism | Female retain the general appereance of juveniles except for the larger abdomen related to the increase of ovarian size | Present | Grizzle, 1985 |
19 | Relative fecundity | Most 6.6-8.0, range 3-12 | 7.3 thousand eggs/kg | Wellborn and Tucker, 1985 |
19 | Relative fecundity | 0.7-12 | 6.35 thousand eggs/kg | Mittelbach and Persson, 1998 |
19 | Relative fecundity | 8 [Usual fecundity of female broodfish] | 8.0 thousand eggs/kg | Legendre et al, 1997 |
19 | Relative fecundity | 5 | 5.0 thousand eggs/kg | Hecht, 1996 |
19 | Relative fecundity | Fecundity => 3,149.8 ± 860.9 (diet 4FO, control), 3967,7 ± 1,229.7 (4PF), 7,676.9 ± 418.8 (10FO), 6,289.3 ± 1,314.9 (10 PF) | 149.8 thousand eggs/kg | Sink and Lochman, 2008 |
20 | Absolute fecundity | 1-1.6 [70 ?] | 1.3 thousand eggs | Internet, 2005 |
20 | Absolute fecundity | 4-34.5 | 19.25 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | 4-35 | 19.5 thousand eggs | Anonymous, 2006 Chapter 3 |
22 | Onset of oogenesis | GSI Increase sugnificantly from September to October and November to January | ['January', 'September', 'October', 'November'] | Mackenzie et al, 1989 |
22 | Onset of oogenesis | A slight increase from November until March | ['January', 'February', 'March', 'November'] | Banks et al, 1999 |
22 | Onset of oogenesis | The average GSI increases in midwinter, in November | ['January', 'February', 'March', 'November'] | Brauhn and McCraren, 1975 |
22 | Onset of oogenesis | Sharp increase in oocyte size in October | ['October'] | Pacoli et al, 1990 |
22 | Onset of oogenesis | August (In South and North Dakota) | ['August'] | June, 1977 |
23 | Intensifying oogenesis activity | April | ['April'] | Mackenzie et al, 1989 |
23 | Intensifying oogenesis activity | A siginificant increase (148%) in April | ['April'] | Banks et al, 1999 |
23 | Intensifying oogenesis activity | June | ['June'] | Brauhn and McCraren, 1975 |
23 | Intensifying oogenesis activity | Second sharp increase of oocyte size from mid-February to May | ['February', 'March', 'April', 'May'] | Pacoli et al, 1990 |
23 | Intensifying oogenesis activity | Beginning of May (In South and North Dakota) | ['May'] | June, 1977 |
24 | Maximum GSI value | 10.9 [June, July] | 10.9 percent | Mackenzie et al, 1989 |
24 | Maximum GSI value | 15.2 [June] | 15.2 percent | Banks et al, 1999 |
24 | Maximum GSI value | 15.6 for prespawning females | 15.6 percent | Grizzle, 1985 |
24 | Maximum GSI value | 15 [GSI usually found in female broodstock] | 15.0 percent | Legendre et al, 1997 |
24 | Maximum GSI value | Mean of 13.8, range 11.0-19.35 [1 July] | 15.18 percent | Brauhn and McCraren, 1975 |
24 | Maximum GSI value | 5% [In May] | 5.0 percent | June, 1977 |
26 | Resting period | About 2 [GSI was low during the summer months: July and August] | 2.0 months | Mackenzie et al, 1989 |
26 | Resting period | About 4 [From July until November] | 4.0 months | Banks et al, 1999 |
26 | Resting period | An apparent low point in the annual ovarian cycle was reached immediatly after spawning | No data | Brauhn and McCraren, 1975 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 5-8 [Not specified] | 6.5 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | 5-8 [Not specified] | 6.5 years | Anonymous, 2006 Chapter 3 |
27 | Age at sexual maturity | 2 [Both sex] | 2.0 years | Olden et al, 2006 |
27 | Age at sexual maturity | Can mature as early as 2 years , but broodfish of at 3 years are preferred [ex not specified] | 2.0 years | Legendre et al, 1997 |
28 | Length at sexual maturity | 36 [Unsexed] | 36.0 cm | Fishbase, 2006 |
28 | Length at sexual maturity | 26.7-40.6 [Both sex] | 33.65 cm | Scott and Crossman, 1973 |
28 | Length at sexual maturity | 27.5 [Both sex] | 27.5 cm | Olden et al, 2006 |
29 | Weight at sexual maturity | Can mature as early as 0.34 kg , but broodfish of at least 1.5 kg are preferred sex not specified] | 0.34 kg | Legendre et al, 1997 |
30 | Male sexual dimorphism | Male assumes a darker body coloration with thick lips | Present | Internet, 2005 |
30 | Male sexual dimorphism | Males at bredding time often brighter blue than otherwise | Present | Scott and Crossman, 1973 |
30 | Male sexual dimorphism | Changes in the external features of sexually active channel catfish occur primarily in males: these changes include widening of the head, increased subcutaneous tissue on dorsal head, and darker skin color. | Present | Grizzle, 1985 |
30 | Male sexual dimorphism | Males were 18 to 43% heavier than females | Absent | Alp et al, 2004 |
30 | Male sexual dimorphism | Secondary sexual characteristics are strongly pronounced. Mature males display a broad, muscular head wider than the body and thickened lips, while head of females remains slender | Absent | Legendre et al, 1997 |
33 | Maximum GSI value | 0.3 | 0.3 percent | Suquet et al, 1994 |
33 | Maximum GSI value | Averages 0.88 during July and 0.69 during November | 0.88 percent | Grizzle, 1985 |
33 | Maximum GSI value | In captivity GSI reaches 0.25 | 0.25 percent | Legendre et al, 1997 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
37 | Spawning migration period | Depending on habitat, the spawners may or may not migrate into rivers or moving water at spawning time | No data | Scott and Crossman, 1973 |
37 | Spawning migration period | Move inshore from deep water, may enter and migrate long distances up tributaries | No data | Goodyear et al. et al, 1982 |
39 | Spawning season | April-June [Sometimes late July-early August] | ['April', 'May', 'June', 'July', 'August'] | Internet, 2005 |
39 | Spawning season | June and July but most spawning activity apperaed to have ended by June | ['June', 'July'] | Mackenzie et al, 1989 |
39 | Spawning season | Spawn in late spring or summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Scott and Crossman, 1973 |
39 | Spawning season | From Mid-April or Mid-May until July | ['April', 'May', 'June', 'July'] | Wellborn and Tucker, 1985 |
39 | Spawning season | Late May to Mid-June | ['May', 'June'] | Kerr and Grant, 1999 |
39 | Spawning season | From May through July | ['May', 'July'] | Rue, 2001 |
39 | Spawning season | Mid-April to August | ['April', 'May', 'June', 'July', 'August'] | Goodyear et al. et al, 1982 |
39 | Spawning season | Late spring and early summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Anonymous, 2006 Chapter 3 |
39 | Spawning season | Mean peak spawning 13 June [Range: 8-30 June] in Lake Oahe, South and North Dakota | ['June'] | June, 1977 |
39 | Spawning season | Fish were allowed to spawn naturally and eggs were collected on June 19 | ['June'] | Rach et al, 2004 |
40 | Spawning period duration | 6-8 [From Mid-April or Mid-May until July] | 7.0 weeks | Wellborn and Tucker, 1985 |
40 | Spawning period duration | 3-4 [Late May to Mid-June] | 3.5 weeks | Kerr and Grant, 1999 |
40 | Spawning period duration | 6-8 [From May through July] | 7.0 weeks | Rue, 2001 |
40 | Spawning period duration | All of the adults that were alive in May spawned naturally during the period from the last week of May to the first week of June | No data | Pacoli et al, 1990 |
41 | Spawning temperature | 21-29 [But optimum around 27-28°C] | 25.0 °C | Internet, 2005 |
41 | Spawning temperature | 23.9-29.5, with 26.7 the apparent optimum | 26.7 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | Begin to spawn when the minimu water temperature exceeds 21°C for several days, normal spawning temperature is from 21 to 29 with 26 considered to be optimal | 21.0 °C | Wellborn and Tucker, 1985 |
41 | Spawning temperature | 22-29 | 25.5 °C | Mittelbach and Persson, 1998 |
41 | Spawning temperature | 21-23.3 up to 29.5 | 22.15 °C | Kerr and Grant, 1999 |
41 | Spawning temperature | 21-29, with 27 being the optimum | 25.0 °C | Rue, 2001 |
41 | Spawning temperature | 65-85°F | 75.0 °C | Goodyear et al. et al, 1982 |
41 | Spawning temperature | 24-29°C | 26.5 °C | Anonymous, 2006 Chapter 3 |
41 | Spawning temperature | 21 [Temperature at which spawning is typically initiated] | 21.0 °C | Olden et al, 2006 |
41 | Spawning temperature | Begin to spawn when the minimum water temperature exceeds 21°C for several days, normal spawning temperature is from 21 to 29 with 26 considered to be optimal | 21.0 °C | Legendre et al, 1997 |
41 | Spawning temperature | Ambient water temperature in all culture facilities ranged from 23 to 27°C. Warm (30°C) water was added if possible to attempt to maintain water temperatures within the defined spawning range | 23.0 °C | Lang and Tiersch, 2007 |
41 | Spawning temperature | 25-27°C optimal spawning temperature | 26.0 °C | Sink and Lochman, 2008 |
42 | Spawning water type | Spawning takes place in seculed, semidark nests; they will not spawn in transparent ponds | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Ponds | Stagnant water | Grizzle, 1985 |
42 | Spawning water type | Nearshore areas, including wetlands, marshes, bays, harbors, and creek mouths, backwaters, pools, and shoals in rivers, especially areas of strong current | Stagnant water | Goodyear et al. et al, 1982 |
43 | Spawning depth | In shallow waters; 2-4 m deep | 3.0 m | Kerr and Grant, 1999 |
43 | Spawning depth | To 42 feet, usually less than 12 feet | 42.0 m | Goodyear et al. et al, 1982 |
44 | Spawning substrate | Undercut banks, under rock ledges, weedy areas, log jams, muskrat burrows | Lithophils | Internet, 2005 |
44 | Spawning substrate | Undercut , log jams, or rocks | Lithophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Hollow logs or cavities in tha bank | No category | Grizzle, 1985 |
44 | Spawning substrate | Spawn under ledges, around or in submerged logs, stumps, or roots and in cavities in the bank | No category | Wellborn and Tucker, 1985 |
44 | Spawning substrate | Cavities, burrows, under rocks near shore; undercut banks, under logs | Lithophils | Kerr and Grant, 1999 |
44 | Spawning substrate | Hollow logs, undercut banks, or stumps, on bottom of rock, rubble, gravel, mud, sand, clay, or vegetation; also on rock breakwalls | Lithophils | Goodyear et al. et al, 1982 |
44 | Spawning substrate | Spawning occurs in natural nests such as undercut banks, muskrat burrows, containers, or submerged logs | No category | Anonymous, 2006 Chapter 3 |
44 | Spawning substrate | In nature, it spawns under edges, around or in submerged logs, stupms or roots and in cavities in the bank | No category | Legendre et al, 1997 |
44 | Spawning substrate | Spawned over rock, rubble, and gravel bottoms of the main river, upstream of the reservoir proper, and in the upper reaches of several of its major tributaries | Lithophils | June, 1977 |
45 | Spawning site preparation | Nests are constructed by one or both parents among the crevices and holes in the rocky jetties | Nest built by both parents | Internet, 2005 |
45 | Spawning site preparation | The pair builds a depression in the ground | No category | Fishbase, 2006 |
45 | Spawning site preparation | Nests built by the male | No category | Scott and Crossman, 1973 |
45 | Spawning site preparation | Male, chooses a spawning, removes silt from the spawning site and defends a territory established around the nest area | No category | Grizzle, 1985 |
45 | Spawning site preparation | The male typically prepares a nest by clearing soft mud and debris from an esaily protected area | No category | Wellborn and Tucker, 1985 |
45 | Spawning site preparation | Male buids nest | No category | Kerr and Grant, 1999 |
45 | Spawning site preparation | Built nest | No category | Rue, 2001 |
45 | Spawning site preparation | Eggs are deposited in nest or burrow made in crevices | Susbtrate chooser | Goodyear et al. et al, 1982 |
45 | Spawning site preparation | Male typically prepares a nest by clearing soft mud and debris from an easily protected area | No category | Legendre et al, 1997 |
47 | Mating system | By pair | Monogamy | Internet, 2005 |
47 | Mating system | By pair, females spawn only once a year but males, at least in the southern USA, "may spawn several times" | Monogamy | Scott and Crossman, 1973 |
47 | Mating system | By pair | Monogamy | Grizzle, 1985 |
47 | Mating system | It takes 4 to 12 hours for a brood fish pair to complete an egg mass with eggs being release five times per gour | No category | Legendre et al, 1997 |
47 | Mating system | Each female was paired with an adult male in a spawning pen | No category | Pacoli et al, 1990 |
47 | Mating system | Females and males are placed in ponds containing spawning containers that stimulate natural nesting sites, and are allowed to form spawning pairs | No category | Lang and Tiersch, 2007 |
48 | Spawning release | This species may spawn more than once a year | Total | Internet, 2005 |
48 | Spawning release | Batch spawners | Multiple | Fishbase, 2006 |
48 | Spawning release | Eggs are deposited in large, flat gelatinous mass | No category | Internet, 2005 |
48 | Spawning release | Spawning lasted 4-6 h with about 9 releases of eggs per hour | No category | Grizzle, 1985 |
48 | Spawning release | Two spawning peaks may occur | No category | Goodyear et al. et al, 1982 |
48 | Spawning release | Sequential spawners. Periodically the female deposits a layer of eggs and the male fertilizes them | No category | Legendre et al, 1997 |
48 | Spawning release | Cluster | Fractional | Hecht, 1996 |
49 | Parity | Return to lakes in fall | Iteroparous | Goodyear et al. et al, 1982 |
49 | Parity | After reaching maturity in nature, reproduce only once year | No category | Legendre et al, 1997 |
49 | Parity | Only one cycle of oogenesis normally occurs each year | No category | Pacoli et al, 1990 |
50 | Parental care | After the spawning, males drive females away from the nest and guard eggs from predators and aerate the eggs until larvae disperse [During incubarion males may eat some eggs] | No category | Internet, 2005 |
50 | Parental care | The males guarding their own egg masses express aggressive behavior | Male parental care | Makeeva and Emel'yanova, 1993 |
50 | Parental care | Nest is guarded by the male | Male parental care | Fishbase, 2006 |
50 | Parental care | Males protect the nest after egg laying, aerate and clean the eggs by fanning with the paired fins, and press and pack the eggs with body and fins | Male parental care | Scott and Crossman, 1973 |
50 | Parental care | After spawning is complete, the male protects the eggs by driving away other fish including the female, the male fans his eggs with his fins [The male continue to guard the young fish for a few days after they hatch] | Male parental care | Grizzle, 1985 |
50 | Parental care | After the male has mated with a female he drives her away and cares for the eggs and fry after hatching | No category | Wellborn and Tucker, 1985 |
50 | Parental care | Males guards nests and young fry | Male parental care | Kerr and Grant, 1999 |
50 | Parental care | One or both adults guard nest and fry until they are about 1 inche long | Biparental care | Goodyear et al. et al, 1982 |
50 | Parental care | After spawning, the male guards the nest for several days | Male parental care | Anonymous, 2006 Chapter 3 |
50 | Parental care | The males assume care of the egg mass after oviposition | Male parental care | Legendre et al, 1997 |
50 | Parental care | Paternal guarder | Male parental care | Hecht, 1996 |