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Revista Brasileira de Zootecnia

On-line version ISSN 1806-9290

R. Bras. Zootec. vol.43 no.2 Viçosa Feb. 2014

http://dx.doi.org/10.1590/S1516-35982014000200001 

AQUACULTURE

 

Dietary phosphorus requirement of pejerrey fingerlings (Odontesthes bonariensis)

 

 

Cleber Bastos Rocha; Mauro Kaster Portelinha; João Morato Fernandes; Aline Conceição Pfaff de Britto; Sérgio Renato Noguez Piedras; Juvêncio Luís Osório Fernandes Pouey

Programa de Pós-Graduação em Zootecnia, Departamento de Zootecnia, Universidade Federal de Pelotas, Pelotas, RS, Brasil

 

 


ABSTRACT

To determine the available phosphorus requirement of pejerrey fish, four semi-purified diets were formulated to contain increasing available phosphorus levels (0.90, 2.7, 5.7 and 8.3 g/kg). Each diet was assigned to groups of 10 fish with average weight of 1.26±0.17 g, distributed into a completely randomized design with four treatments and four replications. Fish were fed at a rate of 10% total biomass four times a day for 60 days. The parameters productive performance, body chemical composition and mineral composition of bones and scales were evaluated. The best productive performance of fingerlings was obtained with the diet containing 4.3 g/kg available phosphorus. The average level of 6.3 g/kg available phosphorus promotes better mineralization of bones and scales in pejerrey fish.

Key Words: bone, fish, food, growth, mineral, nutrition


 

 

Introduction

Phosphorus is one of the most important minerals for fish growth, bone mineralization and lipid and carbohydrate metabolism (Sales and Janssens, 2003; NRC, 2011). However, the phosphorus availability from plant sources is usually low and varies according to the fish species (Boscolo et al., 2005). This occurs because, in cereal grains, phosphorus is in the form of phytic acid, unavailable for monogastrics (Vielma et al., 2002; Raboy, 2009).

Fish in their habitat easily meet their nutritional requirements through the available food in the environment. However, when farmed intensively, their needs have to be met via the diet (Miranda et al., 2000).

Increased fish cultures require the formulation of balanced diets because artificial feed is the only source of nutrition for fish; furthermore, aquaculture effluents high in phosphorus levels contribute to the pollution of the aquatic ecosystem and, eventually, cause eutrophication of natural fresh waters (Coloso et al., 2003; Pezzato et al., 2006).

The pejerrey (Odontesthes bonariensis; Valenciennes [Atheriniformes, Atherinopsidae]) is a native species from Southern Brazil distributed over numerous water bodies around the world (Kopprio et al., 2010).

For most cultivated fish species, phosphorus requirements range from 3 to 15 g/kg of diet (NRC, 2011). However, the phosphorus requirements for pejerrey Odontesthes bonariensis have not been determined. Thus, this study was undertaken to determine the dietary phosphorus requirements for pejerrey fingerlings fed semipurified diets.

 

Material and Methods

The experimental diets were formulated according to the recommendation for the species (Piedras et al., 2004) to contain 550 g/kg crude protein and 3,200 kcal/kg digestible energy. For obtaining a basal diet with low levels of phosphorus, albumin (800 g/kg crude protein) containing 1.72 g/kg total phosphorus was used as protein source. The different levels of total phosphorus (0.9, 2.7, 5.7 and 8.3 g/kg) were obtained by adding sodium phosphate monobasic p.a. to the basal diet at levels of zero (control), 9.0, 22.0 and 35.0 g/kg. The quantity of calcium was about 7 g/kg of the diet (NRC, 2011) by adding calcium carbonate PA (Table 1).

The ingredients were weighed and mixed gradually from low to high volume to facilitate homogenization. After these procedures, they were mixed again in blender with addition of warm water (100 g/kg) to facilitate their homogenization. At the end of this process the mixture was distributed into trays and oven-dried at 50 ºC for approximately 14 hours. These diets were packed and stored in a freezer (-18 ºC) for later use.

The artificial reproduction of pejerrey specimens collected in Lagoa Mangueira/RS was carried out through extrusion to obtain the sexual products (semen and oocytes) and the eggs were incubated in the laboratory. After hatching, these fish were fed zooplankton and powdered commercial fingerling feed (550 g/kg crude protein) and kept in polypropylene box 500 L with recirculation until the beginning of experiment. One hundred and sixty fish with average weight of 1.26±0.17 g which were randomly divided into 16 boxes of polypropylene with 200 L in volume were selected. These experimental units had a biofilter system, artificial aeration with blower central water recirculation and air-conditioned room to maintain water temperature constant.

A completely randomized design with four treatments and four replicates was carried out. All fish were fed powdered commercial fingerling feed for 10 days for subsequent introduction of experimental diets. The feeding rate was 10% biomass distributed four times per day (8.00 h, 10.00 h, 14.00 h. and 17.00 h) and feed leftovers and excrements were siphoned once per day. The experimental period was 60 days. The biometrics was performed at the end by weighing and measuring the animals. The chemical composition of experimental diets was obtained through chemical analysis (AOAC, 1995) and mineral analysis through atomic absorption spectrophotometry. At the beginning of the experimental period 30 fish were euthanized with benzocaine (300 mg/L) and frozen (-18 ºC) to evaluate body chemical composition. At the end of the experiment the same process was performed to all fish. To determine the mineral retention of scales, three animals from each replicate were peeled by scraping with a scalpel blade and the scales were dried at 50 ºC. The spinal bones were kept in warm water (80 ºC) for two minutes and then immediately dissected with tweezers (Furuya et al., 2001). These samples were digested in acid solution (Silva and Queiroz, 2004) and the concentrations of P and Ca were determined in triplicate through atomic absorption spectrophotometry (Tedesco et al., 1995).

The body composition analysis of crude protein, ether extract, ash and moisture was performed using three fish per replicate according to the AOAC (1995). Water quality parameters of dissolved oxygen and temperature (YSI model 55 digital oximeter), pH (AT 310 model potentiometer), total phosphorus (AT-100P model photocolorimeter), alkalinity and total ammonia were monitored three times a week, following the method suggested by APHA (1998).

The fish performance was evaluated using the following formulae: weight gain (g) = final weight (g) - initial weight (g); specific growth rate (% body weight/day) = [(ln final weight - ln initial weight)/days of experiment] × 100; apparent feed conversion ratio = (feed supplied/weight gain) × 100; and survival (%) = [number of fish at the end of the experiment/number of fish at the beginning of the experiment] × 100.

Data were subjected to analysis of variance (ANOVA) and regression analysis (Statistica, version 5.0).

 

Results and Discussion

The physicochemical parameters of the water remained appropriate for the species (Miranda et al., 2006) showing no difference between treatments with the following mean results: temperature 24.78±2.2 ºC, dissolved oxygen 4.85±0.58 mg/L, pH 7.8±0.20, total ammonia nitrogen 0.03±0.0 mg/L, total phosphorus 0.30±0.12 mg/L and total alkalinity 45±5 mg/L.

The weight gain showed quadratic effect with increasing levels of dietary phosphorus. By the fit curve from the equation of regression polynomial, it could be observed that 4.3 g/kg phosphorus result in increased weight gain (Table 2), similar to that recommended by Wilson et al. (1982) for channel catfish (Ictalurus punctatus). For juvenile black seabream (Sparus macrocephalus) the phosphorus requirements of greatest weight gain were 5.5 g/kg (Shao et al., 2008).

A quadratic effect of phosphorus levels on total length, specific growth rate and apparent feed conversion, which were even better until 4.3 g/kg phosphorus in the diet, were observed. For juvenile Nile tilapia (Oreochromis niloticus), Furuya et al. (2008) observed quadratic effect of phosphorus levels on feed conversion, with best level at 4.8 g/kg.

Kim et al. (1998) recommend 7 g/kg available phosphorus for the greatest weight gain of mirror carp (Cyprinus carpio). Ye et al. (2006) evaluated the effect of supplementation with calcium and phosphorus on a purified diet (3 g/kg Ca and 4 g/kg P) for juvenile grouper (Epinephelus coioides), verifying that only phosphorus supplementation (6 g/kg) influenced the weight gain. Survival was not affected by dietary phosphorus levels (P>0.05).

Fontagné et al. (2009) found in a radiographic study that rainbow trout (Oncorhynchus mykiss) fingerlings fed a diet deficient in phosphorus (5 g/kg total phosphorus or zero available phosphorus) showed high incidence of vertebral abnormalities.

The body composition of crude protein and moisture were not affected (P>0.05) by dietary phosphorus levels (Table 3); this result was observed by Lellis et al. (2004) for rainbow trout.

Increased phosphorus levels in the diet reduced body ether extract linearly. The same was observed by Mai et al. (2006), who evaluated the requirements of available phosphorus for yellow croaker (Pseudosciaena crocea) and Zhang et al. (2006), for Japanese sea bass (Lateolabrax japonicus). The increase in available phosphorus probably favored the energy metabolism of fatty acids (β-oxidation), causing a beneficial effect which is the body fat reduction enabling the production of leaner carcasses (Roy and Lall, 2003). This result differs from that observed by Ribeiro et al. (2006), who found no difference in levels of total phosphorus on the deposition of fat, calcium and phosphorus in juvenile Nile tilapia. The body ash increased linearly with increasing levels of phosphorus in the diet; this fact highlights the largest mineral deposition in bones (Figure 1). The same was found by Ye et al. (2006) for juvenile grouper.

 

 

The levels of Ca and P in the vertebrae increased quadratically with increasing levels of phosphorus in the diet (Figure 1). These results are similar to those obtained for other species such as Atlantic salmon (Salmo salar) (Vielma and Lall, 1998), rainbow trout (Bureau and Cho, 1999) and yellow croaker, (Mai et al., 2006). According to Lall and Lewis-McCrea (2007), calcium and phosphorus are closely related to skeletal development and maintenance and vertebrae mineralization.

Dietary phosphorus requirements of pejerrey based on the Ca and P concentrations in the vertebrae were calculated at 6.3 g/kg (Figure 1). Yang et al. (2006) found similar effect for silver perch fingerlings (Bidyanus bidyanus), and minerals gradually increased up to the level of 7.2 g/kg. For juvenile haddock (Melanogrammus aeglefinus), 8.2 g/kg of total phosphorus in the diet was adequate for maximum phosphorus deposition in the vertebrae (Roy and Lall, 2003).

The concentrations of Ca and P in the scales presented a similar trend to that observed in the vertebrae, with a quadratic effect (Figure 2). Phosphorus requirements in the diet based on the composition of Ca and P on the scales were 6.4 and 6.1 g/kg, respectively.

 

 

Differences between the requirements of phosphorus in weight gain and maximum body mineralization can be verified in this study. Zhang et al. (2006) observed similar effects for juvenile Japanese sea bass (Lateolabrax japonicusem), whose requirement was 6.8 g/kg for weight gain and 8.6-9.0 g/kg for bone mineralization. According to Eya and Lovell (1997), important factors such as economic, physiological and environmental factors should be considered when determining the phosphorus requirements in the diet.

 

Conclusions

The requirement of available phosphorus for pejerrey fingerlings is 4.3 g/kg for best productive performance. However, for greater bone mineralization, this requirement increases to 6.3 g/kg.

 

Acknowledgments

The authors thank CAPES/MEC for granting the fellowship to the first author.

 

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Received September 25, 2012 and accepted November 18, 2013.

 

 

Corresponding author: cbr.vet@gmail.com

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