SciELO - Scientific Electronic Library Online

 
vol.14 número2Densidad y tallas de Plicopurpura patula pansa relacionadas con el sustrato y oleaje en la costa rocosa de Guerrero, MéxicoEstudio morfológico y anatómico de las especies reflexas del género Gastroclonium Kützing (Rhodophyceae) índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay artículos similaresSimilares en SciELO

Compartir


Hidrobiológica

versión impresa ISSN 0188-8897

Hidrobiológica vol.14 no.2 Ciudad de México  2004

 

Artículo

 

Effect of the feeding ration on growth performance of Oreochromis mossambicus (Peters) larvae using decapsulated Artemia cysts as dietary supplement

 

Efecto de la ración alimenticia en el crecimiento de larvas de Oreochromis mossambicus (Peters) usando quistes de Artemia decapsulados como suplemento dietético

 

Manuel García-Ulloa Gómez1 and Fernando Hernández-Garciabada

 

Laboratorio de Ciencias Marinas, Universidad Autónoma de Guadalajara, Barra de Navidad, Jalisco, México

 

1Correspondence:
Dr. Manuel García-Ulloa Gómez,
Departamento de Acuacultura, PO Box 3,
Barra de Navidad, Jalisco, C.P. 48987, México.
E-mail: turbotuag@hotmail.com

 

Recibido: 14 de agosto de 2003
Aceptado: 3 de junio de 2004

 

Abstract

Red tilapia larvae Oreochromis mossambicus, were cultured during the 30 days after the onset of the feeding, in order to evaluate different food rations (15, 20, 25, 30 and 35% body-weight/daily) when dried decapsulated Artemia cysts (DDC) were included in a commercial diet as a dietary supplement. Each feeding level was tested with three replicates, and given four times a day. Fish were reared in 10-L plastic containers (n = 40 fish per container) in a water recirculation system. Mean standard length, wet weight and survival were determined at the end of the experiment. Fish larvae growth increased with food ration. There were no differences in fry wet weight results for the 25, 30 and 35% body-weight/daily feeding levels (1.64, 2.05 and 1.94 g, respectively), although decrease in weight gain obtained for the 35% BW/d ration suggest that such food level was higher than the optimum. Survival was not affected for the different feeding rations tested.

Keywords: Tilapia larvae, growth, feeding ration, decapsulated Artemia cysts.

 

Resumen

Se estudió el crecimiento de crías de tilapia roja, Oreochromis mossambicus, durante el primer mes de alimentación exógena, evaluando diferentes raciones alimenticias (15, 20, 25, 30 y 35% del peso corporal/día). Se incluyeron quistes secos y decapsulados de Artemia (DDC) en la dieta comercial como suplemento alimenticio. Cada ración alimenticia se suministró cuatro veces al día, y fueron examinadas por triplicado. Los peces fueron cultivados en contenedores de plástico de 10-L (n = 40 peces por contenedor), conectados a un sistema de recirculación de agua. Al final del experimento, se evaluaron la longitud estándar y peso húmedo promedio, y la sobrevivencia. El crecimiento de las crías se incrementó con el aumento de la ración alimenticia. No se observaron diferencias en el peso húmedo promedio de las crías para los tratamientos 25, 30 y 35% del peso corporal/d (1.64, 2.05 y 1.94 g, respectivamente), aunque el valor obtenido para la ración 35% del peso corporal/d sugiere que tal nivel alimenticio fue mayor que el óptimo. La sobrevivencia no fue afectada por los niveles alimenticios examinados.

Palabras clave: Crías de tilapia, crecimiento, ración alimenticia, quistes decapsulados de Artemia.

 

Introduction

Food quantity and quality have been identified as critical factors for larval fish growth performance (Halver, 1972; Verreth, 1994). Regardless to the food quantity, there are several feeding strategies commonly applied in fish larval growth trails. It is recommended that fry be fed ad libitum or to apparent satiation (Gropp & Tacon, 1994), so that all fish have adequate access to feed. These feeding techniques are widely used for rearing tilapia fry during the first month of exogenous feeding, which represent the culture time when hormonal sex-reversal treatment is applied (Meyer & Smitherman, 1991; Watanabe et al., 1993; Galvez et al., 1996; Siddiqui et al., 1997; Abucay & Mair, 1997). Other studies recommend that due to the rapid growth of tilapia at early stages, feeding ration should be adjusted to better utilization of food and feed waste reduction (Phelps & Popma, 2000), but in many cases, the reported amount of food vary considerably. For instance, MacIntosh and De Silva (1984) fed O. mossambicus (Peters) fry at different food rations (6, 12 and 24% of body weight daily, BW/d). De Silva (1985) and De Silva and Perera (1985) mentioned that a food ration of 6 % of BW/d was adequate to fed Nile tilapia fry. Santiago et al. (1987) fed up to 60 % of the BW/d to O. niloticus (Linnaeus) fry in aquaria, obtaining better growth and survival results fed the larvae with 60% BW/d, when compared with food rations of 30 and 45 % BW/d. Guerrero III et al. (1996) fed tilapia fry with a formulated diet at 10-30 % of their body weight daily. Siddiqui and Al-Harbi (1995) reported 30 % of total biomass/d when feeding tilapia larvae for the first week, thereafter, the feeding rate was reduced to 20, 15 and 10 % of biomass in the following weeks. Phelps and Popma (2000) mentioned that young tilapia fry can consume 20 % or more of their BW/d, suggesting the use of a feeding chart based on anticipated growth to adjust the amount of feed daily.

In relation to the food quality for culturing small tilapia, formulated diets with at least 40 % protein content are commonly used for rearing tilapia larvae and are considered to fulfill the tilapia fry nutritional requirements (National Research Council, 1993). However, there are constraints on the development of tilapia culture in some countries due to the lack of high quality seed for farmers (MacNiven & Little, 2001). Dietary inclusion of high quality supplements in commercial fry diets might improve its growth responses. Although there are some successful feeding experiments on the use of high quality food supplements as live or dried live food for rearing freshwater larvae of several commercial fish species (Verreth et al., 1987; Pector et al., 1994; Weirich et al., 2000), only few reports are found for growing tilapia fry fed with high quality food items (Cruz & James 1989; Lu et al., 2002). Recently, García-Ulloa and Hernández-Garciabada (2003) reported that growth of O. mossambicus fry was improved with the utilization of dried decapsulated Artemia (Kellog) cysts (DDC) as food supplement, suggesting that DDC could be included in the tilapia starter commercial diet, if feeding strategies and techniques, as well as economic considerations, are carefully reviewed. Preliminary results of our research indicated that feeding the tilapia larvae ad libitum with an inclusion of at least 25% of DDC in its commercial diet, produced tilapia juveniles with a mean wet weight of 1.8 g after the first 30 days of feeding, which was similar than the growth obtained for the group of fish fed solely with DDC. However, it is necessary to improve the possible use of DDC in the rearing of tilapia larvae by applying different feeding strategies.

Therefore, the purpose of this study was to find out the effects of different feeding rations (from 15 to 35 % of BW/d) on growth and survival of red tilapia (O. mossambicus) fry, fed with an inclusion of 25% of DDC as a dietary supplement in a commercial diet.

 

Materials and methods

O. mossambicus larvae were produced in indoor fiber glass tanks, by removing fertilized eggs (1-2 d after spawning) from the mouth of 20 incubating adult females of the brood stock held at the Laboratorio de Ciencias Marinas (Universidad Autonoma de Guadalajara, Jalisco, Mexico). Eggs were transferred to McDonald jars until hatching and total yolk absorption occurred. The experiment was conducted using 10 day-old tilapia larvae (initial mean standard length of 7.48 ± 0.38 mm and wet body weight of 8.5 ± 1.7 mg), when larvae were at the onset of the feeding, and lasted for the first 30 d after total yolk absorption. Fifteen plastic containers of 10-L each (filled at 8-L with freshwater) in a closed recirculation system (water flow rate = 0.25 L/min), were stocked with 40 larvae each (García-Ulloa & Hernández-Garciabada, 2003). Temperature and dissolved oxygen were daily measured and maintained at 27 ± 1.2 ºC and higher than 4 mg/L (Chervinski, 1982), respectively, throughout the 30 experimental days. Five feeding rations were tested with three replicates: 15, 20, 25, 30 and 35% of the total BW/d. A tilapia starter diet, TS (API-ABA® 40 % protein, Malta Texo de Mexico, S.A. de C.V., Mexico, D.F.) was grounded and sieved to obtain food particles around 600 to 800 µm diameter. Dried Artemia cysts from the Salt Lake (GREAT LAKE ARTEMIA, Utah, USA) with a hatching efficiency of 85%, were used to prepare the experimental diet. Cysts were decapsulated with a solution of NaOCL, NaOH and water following standardized techniques (Vanhaecke & Sorgeloos, 1982; Sorgeloos et al., 1983). In order to stop the embryo metabolic activity, decapsulated cysts were dried in a laboratory oven (FELISA®, Guadalajara, Mexico) at 40°C (Sorgeloos et al., 1986), until their water content decreased and kept below a level of 9%, which was confirmed by weighing the cysts every 12 hours for 3 days after decapsulation. Finally, TS and dried decapsulated cysts (DDC) were mixed at a proportion of 75%TS/25%DDC, as mentioned by García-Ulloa and Hernández-Garciabada (2003). The proximate composition of the tested diet is given in Table 1.

Fish larvae were fed four times a day between 8:00 and 19:00 hours. Before each feeding, dead animals, feed remnants and faeces were extracted out from the containers by siphoning. The initial total biomass in each container (340 mg) was used to adjust the food ration at experimental day 1. The daily average wet weights of O mossambicus fry for the first 30 days of feeding shown in Table 2, were obtained by conducting a previous study in which larvae were fed at satiation for these first 30 days of feeding with the experimental diet (75%TS/25%DDC), and sampled each day (n = 60) to obtain the daily mean weight values. Mean weight values were used to calculate the daily food ration.

Total larvae from each replicate per treatment, were sampled at the end of the experiment to obtained the mean wet weight and standard length. Prior to weighing, fish were placed on absorbent paper to remove excess of water. The daily weight gain (g/d) was calculated from DWG = (final body weight - initial body weight)/days of culture (Mbahinzireki et al., 2001). The specific growth rate (SGR, % body weight/d) was obtained from SGR = 100 X ([ln Wf - ln Wi]/t), where Wf = mean weight at the end of the period, Wi = mean weight at the beginning of the period, and t = time in days of the period (Ricker, 1979). Survival was calculated by counting total animals per replicate for each diet, after the 30 experimental days. Food conversion ratio (FCR) was obtained from FCR = g feed consumed/g wet weight gained (Al Hafedh et al., 1999). All data were tested for normal distribution and homogeneity of variance before ANOVA was performed (Sokal & Rohlf, 1969). A simple ANOVA analysis was performed and differences between means were compared for significance (α = 0.05) using the Tukey's multiple range test (Reyes, 1982). The statistical analyses were performed using Jandel SigmaStat 2.0 statistical sofware (Jandel Co., USA).

 

Results

The better growth performance of O. mossambicus fry was observed for the fish fed with the 30% BW/d feeding ration (Figure 1). Significantly higher wet weight (P < 0.05) was found for fish fed 30, 35 and 25% BW/d feeding levels than for fish fed lower feeding levels (20 and 15% BW/d). Same trend was observed for the standard length. Significant differences (P < 0.05) were found for the DWG, SGR and FCR among the treatments (Table 3). DWG ranged from 0.0683 g/d for the 30% BW/d treatment, to 0.0428 g/d obtained for the 15% BW/d feeding ration. The higher SGR final value was observed for the 30% BW/d feeding level (18.20%/d). For the FCR, the lowest value (1.61) was shown for the O. mossambicus fry fed with the lowest experimental feeding ration (15% BW/d). The rest of the tested treatments obtained FCR values above 2.00. Survival among treatments did not show differences (P > 0.05) after the 30 experimental days, and fluctuated from 84.16 ± 4.71% for the fry fed with the 30% BW/d feeding ration, to 95.83 ± 4.24% for the tilapia larvae fed with the 20% BW/d feeding level.

 

Discussion

Feed supply influences the growth of fish (Jobbling, 1994), but it turns more critical for the early larval stages since its metabolic requirements vary rapidly with time (Bromage, 1995). One of the most important factors for assessing larval fish growth performance is the study about the relationship between growth and feeding ration. Determining the optimum feed ration should contribute to improving fish larvae production since food is better utilized (Mihelakakis et al., 2001). There are some studies about the effect of feeding ration on the larval growth of various tilapia species. However, growth output results vary considerably. For instance, MacIntosh and De Silva (1984) observed that after the first 30 culture days, growth of O. mossambicus larvae increased with higher food rations (6, 12 and 24% BW/d). They obtained mean weight values that fluctuated from 0.06 to 0.38 g at different stocking densities. Early studies carried out by De Silva and Perera (1984, 1985) and De Silva (1985) considered that 6% BW/d food ration to be more than adequate for rearing of different commercial tilapia species, but growth results varied considerably. In other experiment, Ron et al. (1995) fed O. mossambicus fry at an initial rate of 18% BW/d from day 1 to day 21. Then, ration decreased every 21 days until 4% BW/d. After the first month of feeding, mean weight value was below 0.5 g. Siddiqui and Al-Harbi (1995) worked with O. mossambicus larvae (18.5 mg initial weight) fed them at 30% of total biomass/d in the first culture week, thereafter, it was gradually reduced from 20 to 10% BW/d in the following 5 weeks. In that case, the final individual weight was 0.958 g after 42 culture days. In the Philippines, tilapia fry are commercially reared in net enclosures, concrete tanks and earthen ponds, and fed them with feeding rations varying from 5 to 30 BW/d (Guerrero III et al., 1996), consequently, production output results differ among the different applied culture techniques. Working with blue tilapia (O. aureus, Steindachner) fry, Galvez et al. (1996) obtained a final average weight of 0.65 g after the first 28 days of feeding with a commercial diet, adjusting the feed amount at 15% BW/d.

In the present experiment, food rations tested did influence growth performance of red tilapia larvae after the first month of feeding, using DDC as dietary supplement. Figure 1 indicates that bigger animals were obtained at the 30% BW/d feeding ration (2.05 g mean individual wet weight), showing no differences (p > 0.05) compared with the 25 and 35% BW/d feeding levels. Nevertheless, final weight for the 35% BW/d was lower than the value observed for the 30% BW/d ration. It is well documented that fish growth increases with food ration above the maintenance until it reaches a maximum value at the optimum ration. Then, in rations higher than the optimum, the growth rate declines (Halver, 1972; Hogendoorn, 1983; García-Ulloa, 2000), which could partially explain the reduced mean weight value at the 35% BW/d ration. Generally, plateaus or decreases in weight gain of fish fed diets containing energy levels above the requirement have been observed in some species (Siddiqui et al., 1988; El-Sayed & Teshima, 1992; Lee et al., 2000), coinciding with our results at the higher food ration tested. On the other hand, the highest FCR was observed for the 35% BW/d feeding level (2.50) suggesting that such ration was above the larvae requirement and consequently, food was not well utilized for larval growth (Phelps & Popma, 2000). There were no differences (p > 0.05) in survival among the tested rations. Final survival ranged from 84% for the 30% BW/d ration, to 95% observed for the 20% BW/d feeding level, and were similar to those reported by Galvez et al. (1996), Al-Hafedh et al. (1999) and Olvera-Novoa et al. (2002) working with larvae of different tilapia species. However, our survival results were higher compared with the value reported by Siddiqui and Al-Harbi (1995) for O. mossambicus larvae. Mean DWG and SGR values obtained in our experiment (0.054 g/d and 17.34% weight gain/d, respectively) for the experimental rations, were higher than those reported for the above mentioned works. Such differences in the biological parameters evaluated when compared with other studies could be attributed to several factors as tilapia species, type of food and different food ration used, among others.

Commonly, mean commercial weight of tilapia fry after the first 30 days of exogenous feeding, including an hormone treatment in the diet, vary from 0.2 to 1.0 g (Arredondo-Figueroa et al., 1994; Hulata, 1997; Popma & Rodríguez, 2000; Green & Engle, 2000; MacNiven & Little, 2001). In this study, the mean wet weight of O. mossambicus fry at the end of the experiment, fluctuated from 1.29 for the 15% BW/d feeding level, to 2.05 g for the 30% BW/d food ration. Mihelakakis et al. (2001) pointed out that quality of the feeding ration is one of the most important factors determining the fate of the food consumed and subsequent growth. Under laboratory conditions, DDC have been successfully used in some commercial aquatic species as food supplement (Verreth et al., 1987; Vanhaecke et al., 1990; Pector et al., 1994; Stael et al., 1995; Weirich et al., 2000), since DDC are able to combine the advantages of live and dry diets (Sorgeloos et al., 1977; Vanhaecke et al., 1983). García-Ortega et al. (1998) indicated that the nutritional value and exogenous enzyme contribution of DDC would be responsible dietary factors for successful rearing of different fish larvae. Previous reports showed that our experimental diet (75% commercial diet and 25% DDC) contains 54% crude protein (García-Ulloa & Hernández-Garciabada, 2003), which represents a high protein content. As mention by Church and Pond (1982), the associative or synergistic effects among the dietary elements contained in the ingredients used to elaborate our experimental diet, could explain the final high mean growth values obtained for all tested food rations. There are few reports rearing tilapia fry with high quality dietary items (Cruz & James, 1989; Lu et al., 2002; Olvera-Novoa et al., 2002), but again, due to differences in diets, culture conditions, culture techniques, species and fish age at the beginning of the studies, our results might not be properly compared with the above mentioned works.

Considering the feeding costs related to the possible use of DDC as dietary supplement in rearing of red tilapia larvae, an estimation in the adjustment of the daily food ration to the quantitative requirement of the larvae is of great importance, and represents a very useful tool to reduce production expenditures. Results from the present study suggest that the optimal feeding ration for the growth of O. mossambicus larvae during the first month of exogenous feeding, and including 25% of DDC in its commercial diet, is between 25 and 30% BW/d. Still, much attention should be paid on feeding techniques and strategies, as well as economic considerations, in order to optimize its possible use at commercial level in tilapia hatcheries.

 

References

ABUCAY, J. S. & G. C. MAIR. 1997. Hormonal sex reversal of tilapias: implications of hormone treatment application in closed water systems. Aquaculture Research 28:841-845.         [ Links ]

AL-HAFEDH, Y. S., A. Q. SIDDIQUI, & M. Y. SAIADY. 1999. Effects of dietary protein levels on gonad maturation, size and age at first maturity, fecundity and growth of Nile tilapia. Aquaculture International 7:319-332.         [ Links ]

ARREDONDO-FIGUEROA, J L., FLORES-MUÑOZ, V. F., GONZÁLEZ-TOVAR, F., GARDUÑO-ARGUETA, H. & CAMPOS-VERDUZCO, R. 1994. Desarrollo científico y tecnológico del banco de genoma de tilapia. Secretaria de Pesca, Dirección General de Acuacultura, Convenio SEPESCA/UAM-I, 89 pp.         [ Links ]

BROMAGE, N. 1995. Broodstock management and seed quality-General considerations. In: Bromage, N. & R. J. Roberts (Eds.). Broodstock management and egg and larval quality. Chapter 1, 1-24 p. Blackwell Science. Oxford, UK.         [ Links ]

CHERVINSKY, J. 1982. Environmental physiology of tilapias. In: R. S. V. Pullin & R. H. Lowe-McConnell (Eds.). The biology and culture of tilapias. ICLARM Conference Proceedings. International Center for Living Aquatic Resources Management. Manila, Philippines. Pp. 119-128.         [ Links ]

CHURCH, D.C. & POND, W.G. 1982. Basic animal nutrition and feeding, second edition. John Wiley and Sons. New York, USA. 120 p.         [ Links ]

CRUZ, E. M., & CH. M. JAMES. 1989. The effect of feeding rotifers (Brachionus plicatilis typicus) on the yield and growth of tilapia (Oreochromis spilurus) fry. Aquaculture 77:353-361.         [ Links ]

DE SILVA, S. S. 1985. Performance of Orechromis niloticus (L.) fry maintained on mixed feeding schedules of differing protein content. Aquaculture and Fisheries Management 16:331-340.         [ Links ]

DE SILVA, S. S., & W. M. K. PERERA. 1984. Digestibility in Sarotherodon niloticus fry: effect of dietary protein level and salinity with further observations on variability in daily digestibility. Aquaculture 38:293-306.         [ Links ]

DE SILVA, S. S., & W. M. K. PERERA. 1985. Effects of dietary protein level on growth, food conversion and protein use in young Tilapia nilotica at four salinities. Transnational American Fisheries Society 114:584-589.         [ Links ]

EL-SAYED, A.-F. M. & TESHIMA, S.-I. 1992. Protein and energy requirement of Nile tilapia, Oreochromis niloticus, fry. Aquaculture 103:55-63.         [ Links ]

GALVEZ, J. I., J. R. MORRISON, & R. P. PHELPS. 1996. Efficacy of trenbolone acetate in sex inversion of the blue tilapia Oreochromis aureus. Journal of the World Aquaculture Society 27: 483-486.         [ Links ]

GARCÍA-ORTEGA, A., J. A. J. VERRETH, P. COUTTEAU, H. SEGNER, E. A. HUISMAN, & P. SORGELOOS. 1998. Biochemical and enzymatic characterization of decapsulated cysts and nauplii of the brine shrimp Artemia at different developmental stages. Aquaculture 161:501-514.         [ Links ]

GARCÍA-ULLOA, G. M. 2000. Fundamentos de Nutrición Acuícola. Ed. Folia Universitaria. Universidad Autónoma de Guadalajara. Jalisco, México. 221 p.         [ Links ]

GARCÍA-ULLOA, G. M., 2002. Estimación del peso individual de crías de la tilapia roja Oreochromis mossambicus, durante el primer mes de alimentación usando quistes decapsulados de Artemia como complemento alimenticio. Reporte Técnico No. 57 Laboratorio de Ciencias Marinas, Universidad Autónoma de Guadalajara. 5 p.         [ Links ]

GARCÍA-ULLOA, G. M. & F. HERNÁNDEZ-GARCIABADA 2003. Effect of dietary inclusion of decapsulated Artemia cysts on growth and survival of red tilapia (Oreochromis mossambicus) fry and its subsequent fingerling production. Journal of the Aquaculture in the Tropics 18(2): 139-151.         [ Links ]

GREEN, B. W. & ENGLE, C. R. 2000. Commercial tilapia aquaculture in Honduras. In: B.A. Costa-Pierce & J. E. Rakocy (Eds.) Tilapia Aquaculture in the Americas. Vol. 2. The World Aquaculture Society. Baton Rouge, Louisiana, United States. Pp. 151-170.         [ Links ]

GROPP, J. M. & A. G. J. TACON. 1994. Report of the EIFAC Workshop on Methodology for Determination of Nutrient Requirement in Fish, Eichenau, Germany, 29 June- 1 July 1993. EIFAC Occas. Pap. No. 29. FAO, Rome, 92 pp.         [ Links ]

GUERRERO III, R. D., L. A. GUERRERO, & R. G. CORNEJO. 1996. Tilapia breeding and seed production for brackishwater culture in the Philippines. In: C. L. Marte, G. F. Quintino & A. C. Emata (Eds.). Proceedings of the Seminar-Workshop on Breeding and Seed Production in Cultured Finfishes in the Philippines. SEAFDEC/AQD, Tigbauan, Iloilo, Philippines. Pp. 159-162.         [ Links ]

HALVER, J. E. 1972. Fish nutrition. Academic Press, Inc. London, UK, 713 p.         [ Links ]

HOGENDOORN, H. 1983. Growth and production of the African catfish, Clarias lazera (C. and V.). III. Bioenergetic relations of body weight and feeding level. Aquaculture 35:1-17.         [ Links ]

HULATA, G. 1997. Large-scale tilapia fry production in Israel. The Israeli Journal of Aquaculture-Bamidgeh 49:174-179.         [ Links ]

JOBLING, M. 1994. Fish bioenergetics. Chapman and Hall. London, UK. Pp. 309.         [ Links ]

LEE, S.-M., S. H. CHO, & K.-D. KIM. 2000. Effects of dietary protein and energy levels on growth and body composition of juvenile flounder Paralichthys olivaceus. Journal of the World Aquaculture Society 31:306-315.         [ Links ]

LU, J., G. YOSHIZAKI, K. SAKAI, & T. TAKEUCHI. 2002. Acceptability of raw Spirulina platensis by larval tilapia Oreochromis niloticus. Fisheries Science 68:51-68.         [ Links ]

MACNIVEN, A. M. & D. C. LITTLE. 2001. Development and evaluation of a stress challenge testing methodology for assessment of Nile tilapia (Oreochromis niloticus, Linn.) fry quality. Aquaculture Research 32:671-679.         [ Links ]

MACINTOSH, D. J., & S.S. DE SILVA. 1984. The influence of stocking density and food ration on fry survival and growth in Oreochromis mossambicus and O. niloticus female X O. aureus male hybrids reared in a closed circulated system. Aquaculture 41:345-358.         [ Links ]

MBAHINZIREKI, G. B., K. DABROWSKI, K.-J. LEE, D. EL-SAIDY, & E. R. WISNER. 2001. Growth, feed utilization and body composition of tilapia (Oreochromis sp.) fed with cottonseed meal-based diets in a recirculating system. Aquaculture Nutrition 7:189-200.         [ Links ]

MEYER, D. E., & R. O. SMITHERMAN. 1991. Growth, survival and sex ratios of Oreochromis urolepis hornorum, O. niloticus and their hybrids (O. niloticus female X O. U. hornorum male) treated with 17_-methyltestosterone. Presented at the Third International Symposium on Tilapia in Aquaculture, Abidjan, Cote d'Ivoire, ICLRAM, nov. 11-16, 1991, 13 p.         [ Links ]

MIHELAKAKIS, A., T. YOSHIMATSU, & CH. TSOLKAS. 2001. Effects of feeding rate on growth, feed utilization and body composition of red porgy fingerlings: preliminary results. Aquaculture International 9:237-245.         [ Links ]

NATIONAL RESEARCH COUNCIL 1993. Nutrient requirements of fish. National Academy Press, Washington, D. C., USA. 250 p.         [ Links ]

OLVERA-NOVOA, M. A., C. A. MARTÍNEZ-PALACIOS, & L. OLIVERA-CASTILLO. 2002. Utilization of torula yeast (Candida utilis) as a protein source in diets for tilapia (Oreochromis mossambicus Peters) fry. Aquaculture Nutrition 8:257-264.         [ Links ]

PECTOR, R., W. TACKAERT, P. ABELIN, F. OLLEVIER, & P. SORGELOOS. 1994. A comparative study on the use of different preparations of decapsulated Artemia cysts as food for rearing African catfish (Clarias gariepinus) larvae. Journal of the World Aquaculture Society 25:366-370.         [ Links ]

PHELPS, R. P., & T. J. POPMA. 2000. Sex reversal in tilapia. In: B. A. Costa-Pierce & J. E. Rakocy (Eds.). Tilapia Aquaculture in the Americas. Vol. 2. The World Aquaculture Society. Baton Rouge, Louisiana, United States. Pp. 34-59.         [ Links ]

POPMA, T. J. & RODRIGUEZ, F. B. 2000. Tilapia aquaculture in Colombia. In: B.A. Costa-Pierce & J. E. Rakocy (Eds.). Tilapia Aquaculture in the Americas. Vol. 2. The World Aquaculture Society. Baton Rouge, Louisiana, United States. Pp. 141-150.         [ Links ]

REYES, C. P. 1982. Bioestadística aplicada. Ed. Trillas, S.A. 1ª Edición. México, D.F. 128 p.         [ Links ]

RICKER, W. E. 1979. Growth rates and models. In: W. S. Hoar, D. J. Randall & J. R. Brett (Eds.). Fish physiology, Volume VIII, Bioenergetics and growth. Academic Press. New York, United States. Pp. 599-675.         [ Links ]

RON, B., S. K. SHIMODA, G. K. IWAMA, & E. GORDON GRAU. 1995. Relationships among ration, 17 α-methyltestosterone and growth in the euryhaline tilapia, Oreochromis mossambicus. Aquaculture 135:185-193.         [ Links ]

SANTIAGO, C. B., M. BANES-ALDABA, & M. A. REYES. 1987. Influence of feeding rate and diet form on growth and survival of Nile tilapia (Oreochromis niloticus) fry. Aquaculture 64:277-282.         [ Links ]

SIDDIQUI, A. Q., M. S. HOWLADER, & A. A. ADAM. 1988. Effects of dietary protein levels on growth, feed conversion and protein utilization in fry and young Nile tilapia, Oreochromis niloticus. Aquaculture 70:63-73.         [ Links ]

SIDDIQUI, A. Q., & A. H. AL-HARBI. 1995. Evaluation of three species of tilapia, red tilapia and a hybrid tilapia as culture species in Saudi Arabia. Aquaculture 138:145-157.         [ Links ]

SIDDIQUI, A. Q., A. H. AL-HARBI, & Y. S. AL-HAFEDH. 1997. Effects of food supply on size at first maturity, fecundity and growth of hybrid tilapia, Oreochromis niloticus (L.) X Oreochromis aureus (Steindachner), in outdoor concrete tanks in Saudi Arabia. Aquaculture Research 28:341-349.         [ Links ]

SOKAL, R. R. & F. J. ROHLF. 1969. Biometry. W.H. Freeman. New York, USA. 596 p.         [ Links ]

SORGELOOS, P., E. BOSSUYT, E. LAVINA, M. BAEZA-MESA, & G. PERSOONE. 1977. Decapsulation of Artemia cysts: a simple technique for the improvement of the use of brine shrimp in aquaculture. Aquaculture 12:311-316.         [ Links ]

SORGELOOS, P., E. BOSSUYT, P. LAVENS, P. VANHAECKE, & D. VERSICHELE. 1983. The use of brine shrimp Artemia in crustacean hatcheries and nurseries. In: J. P. McVey & J. R. Moore (Eds.). CRC Handbook of Mariculture, Vol. 1. Crustacean Aquaculture. CRC Press. Boca Raton, Florida, USA. Pp. 71-96.         [ Links ]

SORGELOOS, P., P. LAVENS, P. LÉGER, W. TACKAERT, & D. VERSICHELE. 1986. Manual for the culture and use of brine shrimp Artemia in Aquaculture. Artemia Reference Center, Gent, Belgium. 228 p.         [ Links ]

STAEL, M., T. SANGGONTANAGIT, E. VAN BALLAER, N. PUWAPANICH, A. TUNSUTAPANICH, & P. LAVENS. 1995. Decapsulated cysts and Artemia flakes as alternative food sources for the culture of Penaeus monodon postlarvae. In: P. Lavens, E. Jaspers, & I. Roelants (Eds.), Larvi'95-Fish & Shellfish Larviculture Symposium. European Aquaculture Society, Special Publication No. 24, Gent, Belgium. Pp. 342-345.         [ Links ]

VANHAECKE, P., & P. SORGELOOS. 1982. International Study on Artemia XVIII. The hatching rate of Artemia cysts - a comparative study. Aquacultural Engineering 1:263-273.         [ Links ]

VANHAECKE, P., P. LAVENS &, P. SORGELOOS. 1983. International study on Artemia. XVII. Energy consumption in cysts and early larval stages of various geographical strains of Artemia. Annales de la Société Royale Zoologique de Belgique 113:155-164.         [ Links ]

VANHAECKE, P., L. DE VRIEZE, W. TACKAERT, & P. SORGELOOS. 1990. The use of decapsulated cysts of the brine shrimp Artemia as direct food for carp Cyprinus carpio L. larvae. Journal of the World Aquaculture Society 21:257-262.         [ Links ]

VERRETH, J. 1994. Nutrition and related ontogenetic aspects in larvae of the African catfish Clarias gariepinus. Ph. D. Thesis, Department of Fish Culture and Fisheries, Wageningen Agricultural University. Wageningen, The Netherlands. 205 p.         [ Links ]

VERRETH, J., V. STORCH, & H. SEGNER. 1987. A comparative study on the nutritional quality of decapsulated Artemia cysts, microencapsulated egg diets and enriched dry feeds for Clarias gariepinus (Burchell) larvae. Aquaculture 63:269-282.         [ Links ]

WATANABE, W. O., K. W. MUELLER, W. D. HEAD, & S. C. ELLIS. 1993. Sex reversal of Florida red tilapia in brackish water tanks under different treatment durations of 17-alpha-ethynyltestosterone administered in feed. Journal of Applied Aquaculture 2:29-41.         [ Links ]

WEIRICH, CH. R., R. C. REIGH, & D. W. GLENN III. 2000. Evaluation of decapsulated Artemia cysts in hatchery diets for channel catfish Ictalurus punctatus fry and effects on subsequent fingerling production. Journal of the World Aquaculture Society 31:609-617.         [ Links ]

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons