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Channel catfish

Ictalurus punctatus

Ictalurus punctatus (Channel catfish)
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Distribution
no distribution map available
least concern



Information


Author: María J. Cabrera-Álvarez
Version: B | 2.0 (2022-08-02)

Please note: This part of the profile is currently being revised.


Reviewers: Caroline Marques Maia, Jenny Volstorf
Editor: Jenny Volstorf

Initial release: 2022-08-02
Version information:
  • Appearance: B
  • Last major update: 2022-08-02

Cite as: »Cabrera-Álvarez, María J.. 2022. Ictalurus punctatus (WelfareCheck | farm). In: fair-fish database, ed. fair-fish. World Wide Web electronic publication. First published 2022-08-02. Version B | 2.0. https://fair-fish-database.net.«





WelfareScore | farm

Ictalurus punctatus
LiPoCe
Criteria
Home range
score-li
score-po
score-ce
Depth range
score-li
score-po
score-ce
Migration
score-li
score-po
score-ce
Reproduction
score-li
score-po
score-ce
Aggregation
score-li
score-po
score-ce
Aggression
score-li
score-po
score-ce
Substrate
score-li
score-po
score-ce
Stress
score-li
score-po
score-ce
Malformations
score-li
score-po
score-ce
Slaughter
score-li
score-po
score-ce


Legend

Condensed assessment of the species' likelihood and potential for good fish welfare in aquaculture, based on ethological findings for 10 crucial criteria.

  • Li = Likelihood that the individuals of the species experience good welfare under minimal farming conditions
  • Po = Potential of the individuals of the species to experience good welfare under high-standard farming conditions
  • Ce = Certainty of our findings in Likelihood and Potential

WelfareScore = Sum of criteria scoring "High" (max. 10)

score-legend
High
score-legend
Medium
score-legend
Low
score-legend
Unclear
score-legend
No findings



General remarks

Ictalurus punctatus is a nocturnal catfish species native to North America (St. Lawrence-Great Lakes, Hudson Bay, and Missouri-Mississippi rivers basins) and highly invasive in most of the USA, in some European countries, and Japan. In the US, it is dominating the aquaculture industry; worldwide, its production is highest in China, and it is also cultured in Cuba, Mexico, Russia, and Bulgaria. In aquaculture, it is often hybridised with the related species Ictalurus furcatus, and it can be co-cultured with this and with other species such as Polyodon spathula, Oreochromis niloticus, Pimephales promelas, and Lepomis microlophus. Escapees can be a threat to local populations of FISHES. There is a common high-standard slaughter method in place, and it is cultured with appropriate substrate and depth. However, further information is needed on stress during husbandry procedures and on the proportion of malformations in farms. There are several reports of natural spawning in farming conditions, and there is some potential to improve home range, migration needs, and aggregation needs and to reduce aggression levels.




1  Home range

Many species traverse in a limited horizontal space (even if just for a certain period of time per year); the home range may be described as a species' understanding of its environment (i.e., its cognitive map) for the most important resources it needs access to.

What is the probability of providing the species' whole home range in captivity?

It is unclear for minimal and high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: WILD and FARM: no data found yet.

JUVENILES: WILD: no data found yet. FARM: in-pond raceway: 37.6 m2 (7.7 x 4.9 m) 1, 110 m2 (22 x 5 m) 2; cages: 1.4 m3 (1.2 m ∅), 1.5 m2 (1.2 x 1.2 m), 2.9 m2 (1.2 x 2.4 m), 5.9 m2 (2.4 x 2.4 m) 3; ponds and net pens in reservoirs and lakes 4.

ADULTS: WILD: sedentary, little daily movement for feeding 5. In floodplains: majority at ≤5,000 m, some also >40,000 m 6. In summer: ~15 m/day 7, 60% within their 2,000 m home range 8; in winter: ~10 m/day 7. FARM: daily trips to feeding station following the same route, except in winter, where IND remained in home areas 9 10. Ponds: 16,000 m2, home areas established by groups of IND: 14.3-277.0 m2 10, 40,000-80,000 m2 11; in-pond raceways: 37.6 m2 (7.7 x 4.9 m) 1, 110 m2 (22 x 5 m) 2; ponds and net pens in reservoirs and lakes 4; net cages in reservoirs 12.

SPAWNERS: WILD: no data found yet. FARM: ponds: 16,000 m2 10, 20,000-40,000 m2 13, home areas established by groups of IND: 14.3-277.0 m2 10; individual mating pools 4.




2  Depth range

Given the availability of resources (food, shelter) or the need to avoid predators, species spend their time within a certain depth range.

What is the probability of providing the species' whole depth range in captivity?

It is low for minimal farming conditions, as these do not cover the whole depth range, and it is high for high-standard farming conditions, as it is conceivable that that these will cover the whole depth range after some modifications. Our conclusion is based on a high amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: WILD: 1-2 m 14-13, deep pools 15. FARM: no data found yet.

JUVENILES: WILD: daily movement to shallow riffle areas for feeding 5. <1 m 16, 1-2 m 14-13, non-native waters: ≤5 m but go to surface (1-2 m) if dissolved oxygen is low at larger depths 17; deep pools 15. FARM: ponds: average 1 m 18; in-pond raceways: 1.2 m 1, 2 m 2; cages: 4 m 3.

ADULTS: WILD: 0.3-2.6 m, the larger depth for warmer water in winter 7, 1-2 m 14-13, non-native waters: ≤5 m but go to surface (1-2 m) if dissolved oxygen is low at larger depths 17. FARM: ponds: 0.3-1.0 m depending on temperature and fish size 10; 1.2-1.8 m 11; in-pond raceways: 1.2 m 1, 2 m 2.

SPAWNERS: WILD:  LARVAE and FRY. FARM: ponds: preference for shallow areas in a 0.3-1.0 m deep pond 10.




3  Migration

Some species undergo seasonal changes of environments for different purposes (feeding, spawning, etc.), and to move there, they migrate for more or less extensive distances.

What is the probability of providing farming conditions that are compatible with the migrating or habitat-changing behaviour of the species?

It is low for minimal farming conditions. It is medium for high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

POTAMODROMOUS 19 20. STENOHALINE 21 22 23.

LARVAE and FRY: WILD: pools, small to large rivers, and lakes 15. FARM: tolerate 8 ppt 23, ≤11 ppt 21. LAB: decreasing growth with increasing salinity, with highest growth in fresh water 22.

JUVENILES: WILD: nocturnal 5 16 24. Probably remain in main river until 3-4 years old 25. More abundant in salinities of average 1.7 ppt, but can tolerate ≤11.4 ppt 26-13. FARM: stressed by being caged at ≥ 26.6.°C 3. Tolerate ≤11 ppt 21, ideally kept at <4-6 ppt, mostly kept at <0.5 ppt 27. For details of holding systems crit. 1 and 2.

ADULTS: WILD: nocturnal 5 24. ≤469 km in 72 days 25. In autumn: median 2-11 km 25, ~35 m/day 7 mostly downstream migration from summer home site 25 8 to overwinter in dam, returning in spring 8; in spring: 7-32 km 25 ~65 m/day 7 mostly upstream migration to summer home site 25 8. Probably move into and remain in tributary at 3-6 years old 25. After 38 cm in size, probably move from tributary to main river and remain there for rest of life 25. Some individuals show fidelity for home site 8. More abundant in salinities of average 1.7 ppt, but can tolerate ≤11.4 ppt 26-13. FARM: stressed by being caged at ≥ 26.6.°C 3. Tolerate ≤11 ppt 21, 12 ppt 23, growth slowed at ≥6 ppt 23, ideally kept at <4-6 ppt, mostly kept at <0.5 ppt 27. For details of holding systems crit. 1 and 2.

SPAWNERS: WILD: nocturnal 5 24. FARM: tolerate ≤2 ppt 21. For details of holding systems crit. 1 and 2.




4  Reproduction

A species reproduces at a certain age, season, and sex ratio and possibly involving courtship rituals.

What is the probability of the species reproducing naturally in captivity without manipulation of theses circumstances?

It is low for minimal farming conditions. It is high for high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

WILD: mature at 5 years old 5, water temperature 23-30 °C (optimum: 27 °C) 5. Spawning period Feb-Aug depending on weather and latitude 5, peak in May 5 or June 28. Courtship 29-13 30. Parental care of eggs by males 5. Females spawn once a year, males seldom spawn more than once 5. FARM: mature at 2-3 years old 5. Sex ratio: 1:3-2:3 male:female 31. Stimulation of reproduction by simulating natural habitat temperatures: gametogenesis stimulation by ~1 month of water temperature <10-15 °C 13, spawning stimulation by slow rise to 20-25 °C water temperature 13. Pond: natural spawning 10 32 13 4. Pen and aquarium spawning 32 13 that often involve ovulation induced by hormonal injections 13. After removing eggs from spawning containers, males spawn again 3-4 times 5. LAB: compressed annual thermal cycle advanced maturity from 3 years to 22 months 33.




5  Aggregation

Species differ in the way they co-exist with conspecifics or other species from being solitary to aggregating unstructured, casually roaming in shoals or closely coordinating in schools of varying densities.

What is the probability of providing farming conditions that are compatible with the aggregation behaviour of the species?

It is low for minimal farming conditions. It is medium for high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: WILD: schooling behaviour 34-10. FARM: higher stress at 150-300 IND/m3 than at 50 IND/m3 35.

JUVENILES: WILD: possibly solitary 36 37 or schooling 38. For aggregation and aggression crit. 6. FARM: 256-655 IND/m3 (17.7-92.3 kg/m3) 1, 11,250 IND/ha 11, 13.6 kg/m3 2; cages: 212-494 IND/m3 3, dexreasing oxygen from >318 IND/m3 on 3; overstocking can cause growth and health problems 3. LAB: schooling and shoaling behaviour 39. Lower cortisol levels in solitarily kept FINGERLINGS than in control (0-20 versus 30-40 ng/mL), but no significant difference compared to IND kept in pairs (13-43 ng/mL) 40 and unusually low cortisol levels in all three conditions compared to even the control of another study (100 ng/mL) 41-40. Homogeneity of body sizes and enough space probably more important than number of IND 40. For aggregation and aggression crit. 6.

ADULTS: WILD: possibly solitary 36 37 or schooling 38. Average 21.5 kg/ha, maximum 52 kg/ha 42. For aggregation and aggression crit. 6. FARM: higher stress at 80-215 kg/m3 than at 18 kg/m3 43 and at 14,800-19,800 IND/ha than at 9,800 IND/ha 44. 6,000 IND/ha, with aggregations of same-size IND within home areas of 0.11-0.14 IND/m2 10. Smaller size aggregate more than larger size 10. 198-503 IND/m3 (54.9-199.0 kg/m3) 1, 11,250 IND/ha 11, 13.6 kg/m3 2. Holding ponds: 2,000-3,000 kg/ha (for ADULTS to become SPAWNERS).

SPAWNERS: WILD: no data found yet. FARM: not >900-1,300 kg/ha to avoid missing spawning 13; 6,000 IND/ha 10.




6  Aggression

There is a range of adverse reactions in species, spanning from being relatively indifferent towards others to defending valuable resources (e.g., food, territory, mates) to actively attacking opponents.

What is the probability of the species being non-aggressive and non-territorial in captivity?

It is low for minimal farming conditions. It is medium for high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: WILD and FARMno data found yet.

JUVENILES: WILD: possibly competing for home space 8. FARM: aggressions <212 IND/m3 3; homogeneous body size known to eliminate cannibalism and reduce food competition 1.

ADULTS: WILD: JUVENILES. FARM: hierarchy during feeding 9 and in home areas 10. Chasing of smaller size IND during feeding 9. Smaller IND acclimate to lower temperatures, lower dissolved oxygen levels, and later feeding times to avoid aggressions from larger IND 9. Monthly cropping of large IND does not eliminate hierarchy 9. Homogeneous body size known to eliminate cannibalism and reduce food competition 1. Aggression at low densities 43 like 6 IND/100L 45, decreasing with increased density 43. LAB: aggressions towards same size IND during feeding 9.

SPAWNERS: WILD: males defend nest and eggs and are aggressive towards intruders 5 and females if they return to nest 29-13. FARM: hierarchy during feeding and in home areas 9.




7  Substrate

Depending on where in the water column the species lives, it differs in interacting with or relying on various substrates for feeding or covering purposes (e.g., plants, rocks and stones, sand and mud, turbidity).

What is the probability of providing the species' substrate and shelter needs in captivity?

It is low for minimal farming conditions, as in-pond raceway systems have a concrete basis and cinder block walls, and it is medium for high-standard farming conditions, as provision of shelters need to be confirmed for farming conditions. Our conclusion is based on a high amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: WILD: sand 5 46-13 15, rocks 15, gravel 5 46-13, boulders 46-13, silt 46-13. Complex woody structures 14-13. Moderately turbid water 46-13. FARM: no data found yet.

JUVENILES: WILD: sand, 5 46-13 15, rocks 15, gravel 5 46-13, boulders 46-13, silt 46-13. Dense aquatic weed 5. Preference for clear water, but also common in muddy water 5. Use logs and rocks as shelter 5. Moderately turbid water 46-13. FARM: ponds: 50-90% montmorillonite clay 13. For details of holding systems crit. 1 and 2. LAB: shelter use in shoals during the day 39.

ADULTS: WILD JUVENILES. FARM: ponds: 50-90% montmorillonite clay 13, home areas and swimways to feeder: hard bottom without silt, remaining areas: mud and silt 10.

SPAWNERS: WILD: cavities, crevices, and other confined spaces 5 47-7, preference for semi-dark areas 5; nest in holes in the banks, undercut banks, hollow logs, log jams or rocks 5, probably over rock, rubble or gravel bottoms 28Male builds nest and attracts female 5. FARM: ponds: 50-90% montmorillonite clay 13, home areas and swimways to feeder: hard bottom without silt, remaining areas: mud and silt 10; spawning containers 10 5.




8  Stress

Farming involves subjecting the species to diverse procedures (e.g., handling, air exposure, short-term confinement, short-term crowding, transport), sudden parameter changes or repeated disturbances (e.g., husbandry, size-grading).

What is the probability of the species not being stressed?

It is low for minimal farming conditions. It is medium for high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: FARM: stressed by handling at >30 °C 48. For stress and aggregation crit. 5.

JUVENILES: FARM: stressed by grading due to overcrowding 49, by handling at >20 °C (>30 °C for FINGERLINGS48, by being caged at body size ≥25.4 cm 3. For stress and a) temperature crit. 3, b) aggregation crit. 5. LAB: stressed by low water level 50.

ADULTS: FARM: stressed by grading due to overcrowding 49, by handling at >20 °C 48, confinement 45, by being caged at ≥ 26.6.°C 3. For stress and aggregation crit. 5. LAB: stressed by low water level 50.

SPAWNERS: no data found yet.




9  Malformations

Deformities that – in contrast to diseases – are commonly irreversible may indicate sub-optimal rearing conditions (e.g., mechanical stress during hatching and rearing, environmental factors unless mentioned in crit. 3, aquatic pollutants, nutritional deficiencies) or a general incompatibility of the species with being farmed.

What is the probability of the species being malformed rarely?

It is unclear for minimal and high-standard farming conditions. Our conclusion is based on a medium amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

LARVAE and FRY: risk of deformities at incubation temperature >30 °C 51, higher frequency of spinal deformities when reared in soft than in hard water 52, higher frequency of triple-tail after premature hatching due to low dissolved oxygen concentration compared to natural hatching 53.

JUVENILES: side sprigs 54-13, taillessness 54-13 30, stumpbody 55-56 54-13 30, triple-tail 54-13 53. Taillessness or reduced caudal fins in 1% progeny of stumpbody parents 30. Stumpbody and taillessness not genetically inherited but probably due to environmental aspect 30.

ADULTS:  JUVENILES.




10  Slaughter

The cornerstone for a humane treatment is that slaughter a) immediately follows stunning (i.e., while the individual is unconscious), b) happens according to a clear and reproducible set of instructions verified under farming conditions, and c) avoids pain, suffering, and distress.

What is the probability of the species being slaughtered according to a humane slaughter protocol?

It is high for minimal and high-standard farming conditions. Our conclusion is based on a high amount of evidence.

Likelihoodscore-li
Potentialscore-po
Certaintyscore-ce

Common and high-standard slaughter method: freshwater electro-stunning followed by decapitation 57 58. LAB: efficient stunning with AQUI-S (isoeugenol) followed by CO2 euthanasia 59. Further research needed to confirm for farming conditions.




Side note: Domestication

Teletchea and Fontaine introduced 5 domestication levels illustrating how far species are from having their life cycle closed in captivity without wild input, how long they have been reared in captivity, and whether breeding programmes are in place.

What is the species’ domestication level?

DOMESTICATION LEVEL 5 60, fully domesticated. Cultured since 1914 61-13.


Side note: Forage fish in the feed

450-1,000 milliard wild-caught fishes end up being processed into fish meal and fish oil each year which contributes to overfishing and represents enormous suffering. There is a broad range of feeding types within species reared in captivity.

To what degree may fish meal and fish oil based on forage fish be replaced by non-forage fishery components (e.g., poultry blood meal) or sustainable sources (e.g., soybean cake)?

All age classes: WILD: omnivorous 5, JUVENILES insectivorous 16. FARM: fish meal may be mostly* 62 or completely* 63 replaced, fish oil may be completely* 64 replaced by sustainable sources, but no data found yet for ADULTS and SPAWNERS.

partly = <51% – mostly = 51-99% – completely = 100%




Glossary


ADULTS = mature individuals, for details Findings 10.1 Ontogenetic development
DOMESTICATION LEVEL 5 = selective breeding programmes are used focusing on specific goals 60
FARM = setting in farming environment or under conditions simulating farming environment in terms of size of facility or number of individuals
FINGERLINGS = early juveniles with fully developed scales and working fins, the size of a human finger; for details Findings 10.1 Ontogentic development
FISHES = Using "fishes" instead of "fish" for more than one individual - whether of the same species or not - is inspired by Jonathan Balcombe who proposed this usage in his book "What a fish knows". By referring to a group as "fishes", we acknowledge the individuals with their personalities and needs instead of an anonymous mass of "fish".
FRY = larvae from external feeding on, for details Findings 10.1 Ontogenetic development
IND = individuals
JUVENILES = fully developed but immature individuals, for details Findings 10.1 Ontogenetic development
LAB = setting in laboratory environment
LARVAE = hatching to mouth opening, for details Findings 10.1 Ontogenetic development
POTAMODROMOUS = migrating within fresh water
SPAWNERS = adults during the spawning season; in farms: adults that are kept as broodstock
STENOHALINE = tolerant of a narrow range of salinities
WILD = setting in the wild



Bibliography


1 Brown, Travis W., Jesse A. Chappell, and Claude E. Boyd. 2011. A commercial-scale, in-pond raceway system for Ictalurid catfish production. Aquacultural Engineering 44: 72–79. https://doi.org/10.1016/j.aquaeng.2011.03.003.
2 Wang, Yuyu, Gangchun Xu, Zhijuan Nie, Nailin Shao, Quanjie Li, and Pao Xu. 2019. Growth Performance of Bluntnose Black Bream, Channel Catfish, Yellow Catfish, and Largemouth Bass Reared in the In-Pond Raceway Recirculating Culture System. North American Journal of Aquaculture 81: 153–159. https://doi.org/10.1002/naaq.10082.
3 Swann, LaDon, J E Morris, Dan Selock, and Jean Riepe. 1994. Cage Culture of Fish in the North Central Region. Technical Bulletin Series #110.
4 Zhong, Liqiang, Chao Song, Xiaohui Chen, Wei Deng, Youhong Xiao, Minghua Wang, Qin Qin, Sheng Luan, Jie Kong, and Wenji Bian. 2016. Channel catfish in China: Historical aspects, current status, and problems. Aquaculture 465: 367–373. https://doi.org/10.1016/j.aquaculture.2016.09.032.
5 Wellborn, Thomas, L. 1988. Channel Catfish: Life History and Biology. SRAC Publication 180. Texas Agricultural Extension Service. Texas: College Station.
6 Flotemersch, Joseph E, Donald C Jackson, and John R Jackson. 1997. Channel Catfish Movements in Relation to River Channel-Floodplain Connections: 8.
7 Butler, S. E., and D. H. Wahl. 2011. Distribution, movements and habitat use of channel catfish in a river with multiple low-head dams. River Research and Applications 27: 1182–1191. https://doi.org/10.1002/rra.1416.
8 Pellett, Thomas D. 1998. Seasonal Migration and Homing of Channel Catfish in the Lower Wisconsin River, Wisconsin. North American Journal of Fisheries Management 18: 85–95.
9 Randolph, Kenneth N., and Howard P. Clemens. 1976. Some Factors Influencing the Feeding Behavior of Channel Catfish in Culture Ponds. Transactions of the American Fisheries Society 105: 718–724. https://doi.org/10.1577/1548-8659(1976)105<718:SFITFB>2.0.CO;2.
10 Randolph, Kenneth N., and Howard P. Clemens. 1976. Home Areas and Swimways in Channel Catfish Culture Ponds. Transactions of the American Fisheries Society 105: 725–730. https://doi.org/10.1577/1548-8659(1976)105<725:HAASIC>2.0.CO;2.
11 The Catfish Institute. 2022. Farming and Processing. The Catfish Institute.
12 Wang, Qidong, Lin Cheng, Jiashou Liu, Zhongjie Li, Shouqi Xie, and Sena S De Silva. 2014. Freshwater aquaculture in PR China: trends and prospects. Reviews in Aquaculture: 20.
13 Tucker, C. S., and J. A. Hargreaves. 2004. Biology and Culture of Channel Catfish. Elsevier.
14 Coon, T. G., and H. R. Dames. 1991. Catfish movement and habitat use in a Missouri River tributary. In Proceedings of the Annual Conference Southeastern Association of Fish and Wildlife Agencies, 43:119–132.
15 Page, Lawrence M., and Brooks M. Burr. 2011. Peterson Field Guide to Freshwater Fishes of North America North of Mexico. Houghton Mifflin Harcourt.
16 Yamazaki, Kazuya, Kouki Kanou, and Kazunori Arayama. 2019. Nocturnal activity and feeding of juvenile channel catfish, Ictalurus punctatus, around offshore breakwaters in Lake Kasumigaura, Japan. Ichthyological Research 66: 166–171. https://doi.org/10.1007/s10228-018-0653-4.
17 Mosher, Thomas D. 1983. Effects of Artificial Circulation on Fish Distribution and Angling Success for Channel Catfish in a Small Prairie Lake. North American Journal of Fisheries Management 3: 403–409. https://doi.org/10.1577/1548-8659(1983)3<403:EOACOF>2.0.CO;2.
18 Cole, Brian A., and Claude E. Boyd. 1986. Feeding Rate, Water Quality, and Channel Catfish Production in Ponds. The Progressive Fish-Culturist 48: 25–29. https://doi.org/10.1577/1548-8640(1986)48<25:FRWQAC>2.0.CO;2.
19 Raabe, Joshua K., and Joseph E. Hightower. 2014. Assessing Distribution of Migratory Fishes and Connectivity following Complete and Partial Dam Removals in a North Carolina River. North American Journal of Fisheries Management 34: 955–969. https://doi.org/10.1080/02755947.2014.938140.
20 Favrot, Scott D., and Thomas J. Kwak. 2016. Efficiency of Two-Way Weirs and Prepositioned Electrofishing for Sampling Potamodromous Fish Migrations. North American Journal of Fisheries Management 36: 167–182. https://doi.org/10.1080/02755947.2015.1114537.
21 Perry, W. GUTHRIE, and J. W. Avault. 1968. Preliminary experiment on the culture of blue, channel and white catfish in brackish water ponds. In Proceedings 22nd Annual Conference Southeastern Association of Game and Fish Commissioners, 22:397–406.
22 Altinok, I., and J. M. Grizzle. 2001. Effects of brackish water on growth, feed conversion and energy absorption efficiency by juvenile euryhaline and freshwater stenohaline fishes. Journal of Fish Biology 59: 1142–1152. https://doi.org/10.1111/j.1095-8649.2001.tb00181.x.
23 Tucker, Craig. 2012. Channel Catfish. In Aquaculture: Farming Aquatic Animals and Plants, ed. John S. Lucas and Paul C. Southgate. John Wiley & Sons.
24 Faria, Larissa, Mhairi E. Alexander, and Jean R. S. Vitule. 2019. Assessing the impacts of the introduced channel catfish Ictalurus punctatus using the comparative functional response approach. Fisheries Management and Ecology 26: 570–577. https://doi.org/10.1111/fme.12353.
25 Dames, H. Ross, Thomas G. Coon, and John W. Robinson. 1989. Movements of Channel and Flathead Catfish between the Missouri River and a Tributary, Perche Creek. Transactions of the American Fisheries Society 118: 670–679. https://doi.org/10.1577/1548-8659(1989)118<0670:MOCAFC>2.3.CO;2.
26 Perry Jr, W. Guthrie. 1968. Distribution and relative abundance of blue catfish, Ictalurus furcatus, and channel catfish, Ictalurus punctatus, with relation to salinity. Proceedings of the Southeastern Association of Game and Fish Commissioners 21: 436–444.
27 Tucker, Craig S., and John A. Hargreaves. 2004. Pond Water Quality. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 215–278. Elsevier.
28 June, Fred C. 1977. Reproductive patterns in seventeen species of warmwater fishes in a Missouri River reservoir. Environmental Biology of Fishes 2: 285–296. https://doi.org/10.1007/BF00005995.
29 Baker, J. E. 1985. The All-American Fish. Animal Kingdom. New York Zoological Society, Bronx 19: 23.
30 Dunham, Rex A., R. Oneal Smitherman, and K. Bondari. 1991. Lack of Inheritance of Stumpbody and Taillessness in Channel Catfish. The Progressive Fish-Culturist 53: 101–105. https://doi.org/10.1577/1548-8640(1991)053<0101:LOIOSA>2.3.CO;2.
31 Kelly, Anita M. 2004. Broodfish Management. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 129–144. Elsevier.
32 Wolters, William, R., and Terrence Tiersch R. 2002. Catfish genetics and breeding - Responsible Seafood Advocate. Global Seafood Alliance.
33 Davis, Kenneth B. 2009. Age at puberty of channel catfish, Ictalurus punctatus, controlled by thermoperiod. Aquaculture 292: 244–247. https://doi.org/10.1016/j.aquaculture.2009.04.023.
34 Harlan, J. R., and E. B. Speaker. 1956. Iowa Fish and Fishing. Des Moines: Iowa State Conser. Comm.
35 Refaey, Mohamed M., Dapeng Li, Xing Tian, Zhimin Zhang, Xi Zhang, Li Li, and Rong Tang. 2018. High stocking density alters growth performance, blood biochemistry, intestinal histology, and muscle quality of channel catfish Ictalurus punctatus. Aquaculture 492: 73–81. https://doi.org/10.1016/j.aquaculture.2018.04.003.
36 Oldham, Cydni. 2019. Channel Catfish - Description, Habitat, Image, Diet, and Interesting Facts. Animals Network.
37 Picks, Fisher. 2022. Channel Catfish Size Chart (Captivity vs. Wild).
38 Fry, Brian, Patricia L Mumford, Franklin Tam, Don D Fox, Gary L Warren, Karl E Havens, and Alan D Steinman. 1999. Trophic position and individual feeding histories of fish from Lake Okeechobee, Florida. Canadian Journal of Fisheries and Aquatic Sciences 56: 590–600. https://doi.org/10.1139/f98-204.
39 Brown, B. E., I. Inman, and A. Jearld. 1970. Schooling and Shelter Seeking Tendencies in Fingerling Channel Catfish. Transactions of the American Fisheries Society 99: 540–545. https://doi.org/10.1577/1548-8659(1970)99<540:SASSTI>2.0.CO;2.
40 Wilson, J. Larry, and Lynda L. Roys. 1994. Behavioral Interactions in Juvenile Channel Catfish, Ictalurus punctatus. Journal of Applied Aquaculture 3: 363–382. https://doi.org/10.1300/J028v03n03_12.
41 Strange, R. 1994. Personal communication.
42 Jenkins, Robert M. 1957. The Standing Crop of Fish in Oklahoma Ponds. Proc. Okla. Acad. Sci. 38: 158–172.
43 Klinger, Heiner, Hartmut Delventhal, and Volker Hilge. 1983. Water quality and stocking density as stressors of channel catfish (Ictalurus punctatus Raf.). Aquaculture 30: 263–272. https://doi.org/10.1016/0044-8486(83)90168-0.
44 Ainsworth, A. Jerald, Paul R. Bowser, and Marshall H. Beleau. 1985. Serum Cortisol Levels in Channel Catfish, from Production Ponds. The Progressive Fish-Culturist 47: 176–181. https://doi.org/10.1577/1548-8640(1985)47<176:SCLICC>2.0.CO;2.
45 Davis, Kenneth B., Mary  Anna Suttle, and Nick C. Parker. 1984. Biotic and Abiotic Influences on Corticosteroid Hormone Rhythms in Channel Catfish. Transactions of the American Fisheries Society 113: 414–421. https://doi.org/10.1577/1548-8659(1984)113<414:BAAIOC>2.0.CO;2.
46 Pflieger, William L. 1997. The fishes of Missouri. Rev. ed. Jefferson City: Missouri Dept. of Conservation.
47 Brown, Leo. 1942. Propagation of the Spotted Channel Catfish (Ictalurus Lacustrus Punctatus). Transactions of the Kansas Academy of Science (1903-) 45: 311–314. https://doi.org/10.2307/3625019.
48 Wise, David J., Alvin C. Camus, Thomas E. Schwedler, and Jeffery S. Terhune. 2004. Health management. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 444–502. Elsevier.
49 Tucker, Craig S., Jimmy L. Avery, and David Heikes. 2004. Culture models. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 166–195. Elsevier.
50 Davis, Kenneth B., Billy R. Griffin, and Wayne L. Gray. 2002. Effect of handling stress on susceptibility of channel catfish Ictalurus punctatus to Ichthyophthirius multifiliis and channel catfish virus infection. Aquaculture 214: 55–66. https://doi.org/10.1016/S0044-8486(02)00362-9.
51 Avery, Jimmy L., and James A. Steeby. 2004. Hatchery management. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 145–165. Elsevier.
52 Li, Menghe H., Edwin H. Robinson, and Bruce B. Manning. 2004. Nutrition. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 279–323. Elsevier.
53 Agricultural Research Service. 2014. Improving production efficiency in warm water aquaculture through water quality management. Agricultural Research Service.
54 Dunham, Rex A., and R. Oneal Smitherman. 1987. Genetics and breeding of catfish. Southern cooperative series bulletin (USA).
55 Smitherman, R. O. 1970. Dressing weight (percentage) of normal channel catfish and stubby, deep-bodied fish from Auburn Fisheries Research Unit populations. Alabama Agricultural Experiment Station. Fisheries Research Annual Report 1: 74–76.
56 Smitherman, R.Oneal, Rex A. Dunham, and Douglas Tave. 1983. Review of catfish breeding research 1969–1981 at Auburn University. Aquaculture 33: 197–205. https://doi.org/10.1016/0044-8486(83)90400-3.
57 Silva, Juan L, Gale R Ammerman, and Stuart Dean. 2001. Processing Channel Catfish. Southern Regional Aquaculture Center Publication 183: 1–8.
58 Marshall, Douglas L. 2004. Processing. In Biology and Culture of Channel Catfish, ed. Craig S. Tucker and John A. Hargreaves, 585–600. Elsevier.
59 Bosworth, Brian G., Brian C. Small, Denise Gregory, Jin Kim, Suzanne Black, and Alistair Jerrett. 2007. Effects of rested-harvest using the anesthetic AQUI-STM on channel catfish, Ictalurus punctatus, physiology and fillet quality. Aquaculture 262: 302–318. https://doi.org/10.1016/j.aquaculture.2006.10.035.
60 Teletchea, Fabrice, and Pascal Fontaine. 2012. Levels of domestication in fish: implications for the sustainable future of aquaculture. Fish and Fisheries 15: 181–195. https://doi.org/10.1111/faf.12006.
61 Shira, Austin F. 1917. Notes on the rearing, growth, and food of the channel catfish, Ictalurus punctatus. Transactions of the American Fisheries Society 46: 77–88.
62 Peterson, B.c., N.j. Booth, and B.b. Manning. 2012. Replacement of fish meal in juvenile channel catfish, Ictalurus punctatus, diets using a yeast-derived protein source: the effects on weight gain, food conversion ratio, body composition and survival of catfish challenged with Edwardsiella ictaluri. Aquaculture Nutrition 18: 132–137. https://doi.org/10.1111/j.1365-2095.2011.00878.x.
63 Webster, Carl D., James H. Tidwell, Laura S. Goodgame, Daniel H. Yancey, and Lisa Mackey. 1992. Use of soybean meal and distillers grains with solubles as partial or total replacement of fish meal in diets for channel catfish, Ictalurus punctatus. Aquaculture 106: 301–309. https://doi.org/10.1016/0044-8486(92)90262-J.
64 Santerre, A., M.C. Téllez-Bañuelos, J. Casas-Solís, P. Castro-Félix, M.R. Huízar-López, G.P. Zaitseva, J.L. Horta-Fernández, et al. 2015. Δ6-fatty acid desaturase and fatty acid elongase mRNA expression, phagocytic activity and weight-to-length relationships in channel catfish (Ictalurus punctatus) fed alternative diets with soy oil and a probiotic. Genetics and Molecular Research 14: 11222–11234. https://doi.org/10.4238/2015.September.22.16.


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