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Gelatin in replacement of bovine heart in feed training ofLophiosilurus alexandri in different water salinities

ABSTRACT

The aim of this study was to evaluate commercial gelatin in the total replacement of bovine heart in feed training of "pacamã" Lophiosilurus alexandri in different water salinities. A completely randomized experimental design, in a 2 × 3 factorial arrangement, was performed using two types of moist ingredients (bovine heart and gelatin) and three water salinities (0.0; 2.0 and 4.0 g of salt L-1) with three replications. Juveniles (2.39 ± 0.08 cm standard length and 0.20 ± 0.03 g of weight) were conditioned to accept commercial diets by the technique of the gradual transition of ingredients. At the end of 36 days no differences were observed to weight gain, length gain and specific growth rate. The feed training efficiency was better (P < 0.05) with the gelatin use, 100.0%. There was a negative effect of salinity on the survival rate and management efficiency in the concentration of 4 g of salt L-1, with values of 58.6 ± 12.0 % and 58.0 ± 12.0 %, respectively. Lophiosilurus alexandri juveniles could be feed-trained to accept commercial diets with gelatin in the total replacement of bovine heart in freshwater or salinity of 2 g of salt L-1.

Key words:
carnivorous fish; feed training efficiency; management efficiency; neotropical fish

RESUMO

O objetivo deste estudo foi avaliar o uso de gelatina comercial em substituição total do coração bovino no condicionamento alimentar de pacamãLophiosilurus alexandri em diferentes salinidades da água. O experimento foi realizado em delineamento inteiramente casualizado, em esquema fatorial 2 × 3, usando dois tipos de ingredientes úmidos (coração bovino e gelatina) e três salinidades da água (0,0; 2,0 e 4,0 g de sal L-¹) com três repetições cada. Juvenis (2,39 ± 0,08 cm de comprimento padrão e 0,20 ± 0,03 g de peso) foram condicionados a aceitar dietas comerciais através da técnica da transição gradual de ingredientes. Após 36 dias de experimento não foram observadas diferenças significativas para o ganho de peso, ganho em comprimento e taxa de crescimento específico. A eficiência do condicionamento alimentar foi melhor (P <0,05) com o uso da gelatina (100%). Houve efeito negativo da salinidade da água na sobrevivência e eficiência do manejo na concentração de 4 g de sal L-¹, com valores de 58,6 ± 12,0% e 58,0 ± 12,0%, respectivamente. Juvenis de Lophiosilurus alexandri podem ser condicionados a aceitar dietas comerciais com o emprego da gelatina em substituição total do coração bovino, em água doce ou na salinidade de 2 g de sal L-¹.

Palavras-chave:
peixe carnívoro; eficiência do condicionamento alimentar; eficiência do manejo; peixe neotropical

INTRODUCTION

The production of carnivorous fish is lower than the production of omnivorous fish species, which can be explained by the high cannibalism rate. Due to this, it is necessary to perform the feed training of these species (Cyrino and Kubitza 2003Cyrino JEP and Kubitza F. 2003. Diets for feed training peacock bassCichla sp. Sci Agric 60: 609-613.). Various feed training techniques have been studied, emphasizing the gradual transition of ingredients (Kubitza and Lovshin 1997 Kubitza F and Lovshin LL. 1997. Effects of initial weight and genetic strain on feedtraining largemouth bass Micropterus salmoides using ground fish flesh and freeze dried krill as starter diets. Aquacult148: 179-190., Kasai et al. 2011Kasai RYD, Salaro AL, Zuanon JAS, Sabarense CM, Tavares MM and Campelo DAV. 2011. Training of trairão fingerlings fed with diets containing different levels of vitamin C. R Bras Zootec 40: 463-468., Luz et al. 2011Luz RK, Santos JCE, Pedreira MM and Teixeira EA. 2011. Effect of water flow rate and feed training on "pacamã" (Siluriforme: Pseudopimelodidae) juvenile production. Arq Bras Med Vet Zootec 63: 973-979.). This transition constitutes in the replacement of the moist ingredients (normally bovine heart) for dry diet. However, this technique has some disadvantages, such as the preparation and storage of the diets, and the instability of the pellets, which impairs water quality (Aubin et al. 2009Aubin J, Papatryphon E, Van der Werf HMG and Chatzifotis S. 2009. Assessment of the environmental impact of carnivorous finfish production systems using life cycle assessment. J Clean Prod 17: 354-361.). Thus, is a need to find alternatives for the product normally used as moist ingredient.

Commercial gelatin has been mixed with commercial diets during the feed training of carnivorous fish, but only empirically by fish farmers in the production of "surubins" (Pseudoplatystoma sp.). The use of gelatin showed promising results when used in the feed training of juvenile Hoplias lacerdae (Salaro et al. 2012aSalaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298.).

Another management used in fish production is the salinization of water (Fashina-Bombata and Busari 2003Fashina-Bombata HA and Busari AN. 2003. Influence of salinity on the developmental stages of African catfish Heterobranchus longifilis(Valenciennes, 1840). Aquacult 224: 213-222., Luz and Santos 2010Luz RK and Santos JCE. 2010. Effect of salt addition and feeding frequency on cascudo preto Rhinelepis aspera (Pisces: Loricariidae) larviculture. J Appl Ichthyol26: 453-455. ). For some species of tropical freshwater, low salinity water (2 to 4 g of salt L-1) can be beneficial for the survival and growth of fish. The salinity of the water stimulates feeding and reduces the metabolic rate and feed conversion rate (Altinok and Grizzle 2001Altinok I and Grizzle JM. 2001. Effects of brackish water on growth, feed conversion and energy absorption efficiency by juvenile euryhaline and freshwater stenohaline fishes. J Fish Biol 59: 1142-1152., Luz et al. 2008Luz RK, Martínez-Álvarez RM, De Pedro N and Delgado MJ . 2008. Growth, food intake regulation and metabolic adaptations in goldfish (Carassius auratus) exposed to different salinities. Aquacult276: 171-178. ), in addition to decreasing the energy expenditure with the osmoregulation of animals (Altinok and Grizzle 2001Altinok I and Grizzle JM. 2001. Effects of brackish water on growth, feed conversion and energy absorption efficiency by juvenile euryhaline and freshwater stenohaline fishes. J Fish Biol 59: 1142-1152., Boeuf and Payan 2001Boeuf G and Payan P. 2001. How should salinity influence fish growth? Comp Biochem Physiol 130: 411-423.).

The "pacamã" Lophiosilurus alexandri, is a carnivorous species, of nocturnal habit and easy handling (Tenório et al. 2006Tenório RA, Santos AJG, Lopes JP and Nogueira SEM. 2006. Crescimento do niquim (Lophiosilurus alexandri Steindachner 1876), em diferentes condições de luminosidade e tipos de alimentos. Acta Sci Boil Sci 28: 305-309.). It can reach over 8 kg in nature. This species has been used in restocking programs of the São Francisco River (Guimarães-Cruz et al. 2009Guimarães-Cruz RJ, Santos JE, Sato Y and Veloso-Júnior VC. 2009. Early development stages of the catfish Lophiosilurus alexandriSteindachner, 1877 (Pisces: Pseudopimelodidae) from the São Francisco River basin, Brazil. J Appl Ichthyol 25: 321-327.). Lophiosilurus alexandrihas a firm meat, absence of intramuscular bones and is much appreciated by the culinary sector. Previous studies have demonstrated the positive effect of salinity on larval breeding of this species, when using Artemia nauplii in the feeding (Luz and Santos 2008aLuz RK and Santos JCE. 2008a. Densidade de estocagem e salinidade da água na larvicultura do pacamã. Pesq Agropec Bras 43: 903-909., Santos and Luz 2009Santos JCE and Luz RK. 2009. Effect of salinity and prey concentrations on Pseudoplatystoma corruscans, Prochilodus costatus and Lophiosilurus alexandri larviculture. Aquacult287: 324-328.), which indicates the need for further study on water salinity in the remaining stages of the production of this species.

The objective of this study was to evaluate commercial gelatin in the total replacement of bovine heart in the feed training of Lophiosilurus alexandri in different water salinities.

MATERIALS AND METHODS

This experiment was approved by the Ethics Committee of Department of Animal Science, UFV (Protocol N 19/2014).

Experimental Design and Fish Growth

After absorption of the yolk sac, the Lophiosilurus alexandrilarvae were kept in freshwater and fed with Artemianauplii for a period of 30 days. After this period, the juveniles with standard length of 2.39 ± 0.08 cm and weight of 0.20 ± 0.03 g were stocked (5 fish L-1) in 18 aquariums (35 × 30 × 14 cm) containing five liters of water, a biological filter, constant aeration and controlled temperature (27.0 ± 1.0 ºC) through the use of a heater and thermostat. The aquariums were covered with a screen of 2 mm in diameter to prevent fish from escaping. The aquariums were kept in a 12 h of photophase by fluorescent lamps (60 W).

A completely randomized experimental design, in a 2 × 3 factorial arrangement was performed using two types of moist ingredients (bovine heart and gelatin) and three water salinities (0.0; 2.0 and 4.0 g of salt L-1) with three replications. A commercial common salt (Cisne(r), Brazilian Industry - 390 mg sodium g-1 of salt, 25 μg iodine g salt-1) was used to create the different salinities. The salt was dissolved in the water of the aquariums prior to distribution of the fish. The fish were transferred directly from freshwater to the different salinity waters.

The fish were conditioned to accept commercial diets by the technique of gradual transition of ingredients in accordance to Salaro et al. (2012a)Salaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298., with modifications to the transition time of the last diet. The diets were made using commercial diets (41.0% crude protein, 8.0% ether extract, 9.5% ash, 4490.0 kcal kg-1 gross energy) as dry ingredients and bovine heart or commercial gelatin powder (Gelita(r)) as moist ingredients. The gelatin was dissolved in water at 50 °C and mixed with ration powder in accordance to Salaro et al. (2012a)Salaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298. (Table I). All diets were stored in a freezer (-18 °C) and thawed daily to make the pellets (1 mm) just before the feeding of the fish.

TABLE I
Quantity of ingredients and number of days of the diets used in the feed training of Lophiosilurus alexandrijuveniles.

The chemical composition of feed ingredients (Table II) was analyzed following the Association of Official Analytical Chemists methods (AOAC 1999AOAC - Association of Official Analytical Chemists. 1999. Official Methods of Analysis of Official Analytical Chemists International. 16th ed., Association of Official Analytical Chemists Inc., Washington, DC, p. 1141.). The crude protein (total nitrogen 6.25) was measured using the Kjeldahl method after acid digestion. The total lipids content was estimated using the Soxhlet apparatus method. The moisture was determined by drying the sample at 105 °C for 24 h to a constant weight. The ash was determined by incinerating the dried sample in a muffle furnace at 550 °C for 12 h. These analyses were performed in the Food Analysis Laboratory, Department of Animal Science, Federal University of Viçosa, Brazil.

TABLE II
Calculated chemical composition (g kg-1 dry matter) of diets used in feed training of Lophiosilurus alexandri.

The Lophiosilurus alexandri juveniles were hand fed to apparent satiety, three times a daily, at 08:00, 13:00 and 18:00 h. During the feeding of the fish, the aquariums were verified and the dead fish were removed and quantified. Every day, at 18:30 h, 100% of the water volume of each aquarium was changed. During this procedure, which lasted about 30 sec, juveniles were caught with a net and immediately transferred into another clean aquarium under the same experimental conditions (temperature and salinity water). This procedure is routine in the feed training of carnivorous fish in the Fish Nutrition Laboratory of the Department of Animal Biology of the Federal University of Viçosa. This management is performed with the aim of maintaining water quality due to the characteristics of the ingredients used in feed training. The water oxygen concentration was maintained above 6.50 ± 1.0 mg L-1 by a supplemental aeration system. The pH was 8.10 ± 0.56 and the total ammonia was lower than 0.02 mg L-1. Water parameters were measured with Multiparameter Meter (model HI 9828, Hanna Instruments, Brazil).

Biometric Index

At the end of the experiment (36 days), all fish were counted, weighed on a precision scale (model MB45 Toledo (r) 0.001 g) and their standard lengths were measured with a digital caliper (model series 500 Absolute Coolant Proof (r) of 0.0001 m) for the calculation of weight gain (WG), length gain (LG), specific growth rate (SGR), survival rate (SR), the feed training efficiency (FTE), and the management efficiency (ME).

Specific growth rate (SGR) of fish were calculated according to the expression: SGR = 100 × (lnWf− lnWi)/Δt, where Wi and Wf are the initial and final weights (in grams). The feed training efficiency (FTE) was calculated following the expression: FTE = NCF/NLF x 100, where NCF = number of conditioned fish (fish with body weight 20% greater than the initial average weight) and NLF = number of live fish. The management efficiency (ME) was calculated following the expression: ME = FTE x SR/100.

Statistical Analyses

Data were analyzed using Factorial Anova, and means were compared by SNK test, at 5% significance. The percentage results were arcsine transformed but only the percent results are presented.

RESULTS

No differences were observed between the moist ingredients (bovine heart or gelatin), water salinities and the interaction between them (P > 0.05) for weight gain, length gain and specific growth rate. The feed training efficiency was better for the fish conditioned with gelatin (P < 0.05). Salinity effects were observed on survival rate and the management efficiency (P < 0.05), the lower rates of both parameters were verified at 4 g of salt L-1 (Table III).

TABLE III
P values and average (±SD) of survival rate (SR), weight gain (WG), length gain (LG), specific growth rate (SGR), feed training efficiency (FTE) and efficiency of management (EM) of juveniles ofLophiosilurus alexandri to feed training with two moist ingredients (bovine heart or gelatin) and three water salinities, for a total of 36 days of experiment.

DISCUSSION

The lack of difference in weight and length gains and the specific growth rate of fish, using gelatin as a replacement of bovine heart, can probably be explained by the greater stability of the pellets on the water, facilitating the seizure and intake of food by fish. These results show the possibility of using gelatin as a moist ingredient in feed training of Lophiosilurus alexandri as found by Hoplias lacerdae (Salaro et al. 2012aSalaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298.). Thus, studies using gelatin for others carnivorous species should be performed.

The best feed training efficiency of fish, achieved by those fed diets containing gelatin, indicates the good palatability of these diets for Lophiosilurus alexandri. However, for Hoplias lacerdae, the use of gelatin afforded lower feed training efficiency than that observed with bovine heart, requiring supplementation with fish meal to obtain the feed training efficiency equivalent to diets with bovine heart (Salaro et al. 2012aSalaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298.). These results reinforce that palatability of the diet is species-specific (Kasumyan and Tinkova 2013Kasumyan AO and Tinkova TV. 2013. Taste Attractiveness of Different Hydrobionts for Roach Rutilus rutilus, BitterlingRhodeus sericeus amarus, and Rainbow TroutOncorhynchus mykiss. J Ichthyol 53: 499-508.).

The lower survival rate of fish in salinity 4 g of salt L-1 may be related to the development phase of the animals (Fashina-Bombata and Busari 2003Fashina-Bombata HA and Busari AN. 2003. Influence of salinity on the developmental stages of African catfish Heterobranchus longifilis(Valenciennes, 1840). Aquacult 224: 213-222.) and the time of exposure to water salinity. Larvae of Lophiosilurus alexandri with 12 days of age support salinity up to 6 g of salt L-1 for 96 h (Luz and Santos 2008bLuz RK and Santos JCE. 2008b. Avaliação da tolerância de larvas do pacamã Lophiosilurus alexandri Steindachner, 1877 (Pisces: Siluriformes) a diferentes salinidades. Acta Sci 30: 345-350.). It is possible that the lower survival rate is also associated with stress related to constant changes in diets (Barcellos et al. 2000Barcellos LJG, Souza SMG and Woehl VM. 2000. Estresse em peixes: fisiologia da resposta ao estresse, causas e consequências. Bol Inst Pesca 26: 99-111.) and the daily changes of water aquariums (Salaro et al. 2012bSalaro AL, Campelo DAV, Pontes MD, Tavares MM, Zuanon JAS and Luz RK. 2012b. Saline water for juvenile giant trahira during feed training. R Bras Zootec41: 1342-1345.). Fish more susceptible to stress are less well suited to tolerate multiple stressors and require a long time period to adapt to saline water (Fevolden et al. 2003Fevolden SE, Røed KH and Fjalestad K. 2003. A combined salt and confinement stress enhances mortality in rainbow trout (Oncorhynchus mykiss) selected for high stress responsiveness. Aquacult216: 67-76.).

In the larviculture of freshwater fish as Lophiosilurus alexandri(Luz and Santos 2008bLuz RK and Santos JCE. 2008b. Avaliação da tolerância de larvas do pacamã Lophiosilurus alexandri Steindachner, 1877 (Pisces: Siluriformes) a diferentes salinidades. Acta Sci 30: 345-350.),Pseudoplatystoma corruscans (Santos and Luz 2009Santos JCE and Luz RK. 2009. Effect of salinity and prey concentrations on Pseudoplatystoma corruscans, Prochilodus costatus and Lophiosilurus alexandri larviculture. Aquacult287: 324-328.) and Pimelodus maculatus (Weingartner and Zaniboni Filho 2004Weingartner M and Zaniboni Filho E. 2004. Efeito de fatores abióticos na larvicultura de pintado amarelo Pimelodus maculatus (Lacépède, 1803): salinidade e cor de tanque. Acta Sci26: 151-157.), 2 g of salt L-1can be used, whereas larvae of Prochilodus costatus (Santos and Luz 2009Santos JCE and Luz RK. 2009. Effect of salinity and prey concentrations on Pseudoplatystoma corruscans, Prochilodus costatus and Lophiosilurus alexandri larviculture. Aquacult287: 324-328.),Piaractus mesopatamiscus (Jomori et al. 2012Jomori RK, Luz RK and Portella MC. 2012. Effect of Salinity on Larval Rearing of Pacu, Piaractus mesopotamicus, a Freshwater Species. J World Aquacult Soc 43: 423-432.) and Hoplias lacerdae (Luz and Portella 2002Luz RK and Portella MC. 2002. Larvicultura de trairão (Hoplias lacerdae) em água doce e água salinizada. R Bras Zootec31: 829-834.) can be reared at 4 g of salt L-1. Furthermore, 6 g of salt L-1 was tolerated byRhinelepis aspera during the larviculture (Luz and Santos 2010Guimarães-Cruz RJ, Santos JE, Sato Y and Veloso-Júnior VC. 2009. Early development stages of the catfish Lophiosilurus alexandriSteindachner, 1877 (Pisces: Pseudopimelodidae) from the São Francisco River basin, Brazil. J Appl Ichthyol 25: 321-327.), showing different salinity tolerances among different fish species.

The lower survival rate could also be related to an osmotic imbalance of the fish at 4 g of salt L-1. The increasing salinity of the water can lead to a number of metabolic and physiological changes (Boeuf and Payan 2001Boeuf G and Payan P. 2001. How should salinity influence fish growth? Comp Biochem Physiol 130: 411-423., Luz et al. 2008). This fact was also previously observed for juvenile of Hoplias lacerdae during feed training in different water salinities (Salaro et al. 2012bSalaro AL, Campelo DAV, Pontes MD, Tavares MM, Zuanon JAS and Luz RK. 2012b. Saline water for juvenile giant trahira during feed training. R Bras Zootec41: 1342-1345.). However, the use of specific salinities can reduce stress and decrease susceptibility to diseases, as well as preserve and control pathogens (Altinok and Grizzle 2001Altinok I and Grizzle JM. 2001. Effects of brackish water on growth, feed conversion and energy absorption efficiency by juvenile euryhaline and freshwater stenohaline fishes. J Fish Biol 59: 1142-1152., Garcia et al. 2007Garcia LO, Becker AG, Copatti CE and Baldisseroto B. 2007. Salt in the food and water as a supportive therapy for Ichthyophthirius multifiliis infestation on Silver catfish, Rhamdia quelen, fingerlings. J World Aquacult Soc 38: 1-11.). For Hoplias lacerdae, salinity up to 5 g of salt L-1 attenuated stress during feed training (Salaro et al. 2012aSalaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298.).

In conclusion, Lophiosilurus alexandri juveniles can be feed-trained to accept commercial diets with gelatin as a replacement for bovine heart in freshwater or salinity of 2 g of salt L-1.

ACKNOWLEDGMENTS

We wish to thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and the Fundação de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG), for providing financial support for this project.

REFERENCES

  • Altinok I and Grizzle JM. 2001. Effects of brackish water on growth, feed conversion and energy absorption efficiency by juvenile euryhaline and freshwater stenohaline fishes. J Fish Biol 59: 1142-1152.
  • AOAC - Association of Official Analytical Chemists. 1999. Official Methods of Analysis of Official Analytical Chemists International. 16th ed., Association of Official Analytical Chemists Inc., Washington, DC, p. 1141.
  • Aubin J, Papatryphon E, Van der Werf HMG and Chatzifotis S. 2009. Assessment of the environmental impact of carnivorous finfish production systems using life cycle assessment. J Clean Prod 17: 354-361.
  • Barcellos LJG, Souza SMG and Woehl VM. 2000. Estresse em peixes: fisiologia da resposta ao estresse, causas e consequências. Bol Inst Pesca 26: 99-111.
  • Boeuf G and Payan P. 2001. How should salinity influence fish growth? Comp Biochem Physiol 130: 411-423.
  • Cyrino JEP and Kubitza F. 2003. Diets for feed training peacock bassCichla sp. Sci Agric 60: 609-613.
  • Fashina-Bombata HA and Busari AN. 2003. Influence of salinity on the developmental stages of African catfish Heterobranchus longifilis(Valenciennes, 1840). Aquacult 224: 213-222.
  • Fevolden SE, Røed KH and Fjalestad K. 2003. A combined salt and confinement stress enhances mortality in rainbow trout (Oncorhynchus mykiss) selected for high stress responsiveness. Aquacult216: 67-76.
  • Garcia LO, Becker AG, Copatti CE and Baldisseroto B. 2007. Salt in the food and water as a supportive therapy for Ichthyophthirius multifiliis infestation on Silver catfish, Rhamdia quelen, fingerlings. J World Aquacult Soc 38: 1-11.
  • Guimarães-Cruz RJ, Santos JE, Sato Y and Veloso-Júnior VC. 2009. Early development stages of the catfish Lophiosilurus alexandriSteindachner, 1877 (Pisces: Pseudopimelodidae) from the São Francisco River basin, Brazil. J Appl Ichthyol 25: 321-327.
  • Jomori RK, Luz RK and Portella MC. 2012. Effect of Salinity on Larval Rearing of Pacu, Piaractus mesopotamicus, a Freshwater Species. J World Aquacult Soc 43: 423-432.
  • Kasai RYD, Salaro AL, Zuanon JAS, Sabarense CM, Tavares MM and Campelo DAV. 2011. Training of trairão fingerlings fed with diets containing different levels of vitamin C. R Bras Zootec 40: 463-468.
  • Kasumyan AO and Tinkova TV. 2013. Taste Attractiveness of Different Hydrobionts for Roach Rutilus rutilus, BitterlingRhodeus sericeus amarus, and Rainbow TroutOncorhynchus mykiss J Ichthyol 53: 499-508.
  • Kubitza F and Lovshin LL. 1997. Effects of initial weight and genetic strain on feedtraining largemouth bass Micropterus salmoides using ground fish flesh and freeze dried krill as starter diets. Aquacult148: 179-190.
  • Luz RK, Martínez-Álvarez RM, De Pedro N and Delgado MJ . 2008. Growth, food intake regulation and metabolic adaptations in goldfish (Carassius auratus) exposed to different salinities. Aquacult276: 171-178.
  • Luz RK and Portella MC. 2002. Larvicultura de trairão (Hoplias lacerdae) em água doce e água salinizada. R Bras Zootec31: 829-834.
  • Luz RK and Santos JCE. 2008a. Densidade de estocagem e salinidade da água na larvicultura do pacamã. Pesq Agropec Bras 43: 903-909.
  • Luz RK and Santos JCE. 2008b. Avaliação da tolerância de larvas do pacamã Lophiosilurus alexandri Steindachner, 1877 (Pisces: Siluriformes) a diferentes salinidades. Acta Sci 30: 345-350.
  • Luz RK and Santos JCE. 2010. Effect of salt addition and feeding frequency on cascudo preto Rhinelepis aspera (Pisces: Loricariidae) larviculture. J Appl Ichthyol26: 453-455.
  • Luz RK, Santos JCE, Pedreira MM and Teixeira EA. 2011. Effect of water flow rate and feed training on "pacamã" (Siluriforme: Pseudopimelodidae) juvenile production. Arq Bras Med Vet Zootec 63: 973-979.
  • Salaro AL, Campelo DAV, Pontes MD, Tavares MM, Zuanon JAS and Luz RK. 2012b. Saline water for juvenile giant trahira during feed training. R Bras Zootec41: 1342-1345.
  • Salaro AL, Oliveira Jr JC, Pontes MD, Oliveira KRB, Neves IGAA, Ferraz RB, Hisano H and Zuanon JAS. 2012a. Replacement of moist ingredients in the feed training of carnivorous fish. R Bras Zootec41: 2294-2298.
  • Santos JCE and Luz RK. 2009. Effect of salinity and prey concentrations on Pseudoplatystoma corruscans, Prochilodus costatus and Lophiosilurus alexandri larviculture. Aquacult287: 324-328.
  • Tenório RA, Santos AJG, Lopes JP and Nogueira SEM. 2006. Crescimento do niquim (Lophiosilurus alexandri Steindachner 1876), em diferentes condições de luminosidade e tipos de alimentos. Acta Sci Boil Sci 28: 305-309.
  • Weingartner M and Zaniboni Filho E. 2004. Efeito de fatores abióticos na larvicultura de pintado amarelo Pimelodus maculatus (Lacépède, 1803): salinidade e cor de tanque. Acta Sci26: 151-157.

Publication Dates

  • Publication in this collection
    27 Nov 2015
  • Date of issue
    Oct-Dec 2015

History

  • Received
    28 Oct 2014
  • Accepted
    09 Mar 2015
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