Performance
of poly cultured fish species fed organic or commercial diets
Desempenho
de peixes em policultivo alimentados com ração
orgânica e comercial
Rendimiento
de peces en policultivo alimentados con
dietas orgánica y comercial
Betina
Muelbert1, Marcos Weingartner1, Ricardo Yuji Sado2, Fernanda Ferrari2, Maude
Regina de Borba1
1Professores Doutores da Universidade Federal da
Fronteira Sul, Laranjeiras do Sul, Paraná. +55423635-8691. E-mails: betina.muelbert@uffs.edu.br; marcos.weingartner@uffs.edu.br;
maude.borba@uffs.edu.br. 2Professores
Doutores da Universidade Tecnológica Federal do Paraná. Dois Vizinhos, Paraná.
E-mails: ricardoysado@utfpr.edu.br;
fernandaferrari@utfpr.edu.br.
Recebido: 28/04/2020; Aprovado: 24/09/2020
Key
words: Organic aquaculture; Rhamdia quelen; Fish farming; Nutrición.
Resumo: Para a produção de peixes orgânicos o sistema de policultivo
é indicado. O objetivo deste estudo foi verificar o desempenho de peixes
criados em sistema de policultivo, alimentados com
dieta orgânica ou comercial, em experimento de campo realizado no sul do
Brasil. O policultivo compreendeu a combinação de
espécies com diferentes hábitos alimentares: Rhamdia quelen (30%), Cyprinus
carpio (20%), Pterygoplichthys joselimaianus
(15%), Prochilodus lineatus
(15%) Hypophthalmichthys molitrix (7,5%), H.
nobilis (7,5%) e Ctenopharyngodon
idella (5%), distribuídas (1,5 peixe m-2)
em viveiros escavados de quatro propriedades rurais, em delineamento em blocos casualizados. Foram avaliados dois tratamentos alimentares,
dieta orgânica artesanal peletizada e dieta
convencional comercial extrusada, ao longo de 12
meses. Ao final do período de cultivo sobrevivência média, peso médio final,
taxa de crescimento específico e composição do filé não diferiram entre os
tratamentos dietéticos. Todavia, foi obtida produtividade média significativamente
maior nos viveiros em que os peixes foram alimentados com a dieta orgânica
(4.877,8kg ha-1) em comparação aos que receberam a dieta comercial
(3.067,1 kg ha-1). Conclui-se que a
suplementação alimentar com dietas orgânicas peletizadas
registrou maior produção do que dieta comercial neste sistema de policultivo. Esperamos que estes resultados estimulem mais
pesquisas sobre a piscicultura orgânica.
Palavras-chave: aquicultura orgânica; Rhamdia quelen; piscicultura; nutrição.
Palabras
Clave: Acuacultura orgánica; Rhamdia quelen; Piscicultura;
Nutrición.
INTRODUCTION
Fish farming generates income
and is a valuable source of highly nutritious animal protein (FAO, 2016). The
recent increase in fish consumption and market share of organic foods have
raised attention to organic aquaculture. Especially for small-scale fish
farming operations, organic aquaculture can become a development model (PAUL;
VOGL, 2013; BEG et al., 2016). Organic production systems must follow
principles and guidelines that are based on national regulations. The Brazilian
organic aquaculture regulation is the IN 28/2011and establishes, amongst many
recommendations, the use of polyculture, prioritizing native species (BRASIL,
2011).
Fish polyculture benefits
species synergistically and enhances nutrient cycling in environment. The
combination of fishes with different feeding habits (omnivorous, herbivorous
and filter feeders) ensures the consumption of all kinds of natural organisms
in the pond. Consequently, it is possible to obtain elevated growth rates and
biomass due to these complementary interactions among fish species (HAO-REN,
1982).
Fish polyculture systems in
southern Brazil are predominately based around small-scale farming units.
Usually is a mixture of common carp Cyprinus carpio, silver carp Hypophthalmichthys
molitrix, bighead carp H. nobilis and
grass carp Ctenopharyngodon idella. Some studies have been conducted to
introduce other species such as silver catfish (Rhamdia
quelen) and Nile tilapia (Oreochromis niloticus) (SILVA et al., 2008; BARCELOS et al., 2012)
and on farm inputs and commercial diets as supplementary feeding in polyculture
(HERNANDEZ et al., 2014).
Although not essential in
low-density systems supplementary feeding is crucial in more intensive
polyculture systems as natural food production in the pond becomes insufficient
to enhance production. With this in mind, artificial feed supplementation in an
organic system must be produced in accordance to standards, i.e. manufactured
with organic ingredients. Moreover, fishmeal should not be refined and the use
of synthetic and genetically modified ingredients in feedstuffs are not allowed
(BRASIL, 2011). Some authors have studied performances of fish fed organic
diets (DIETERICH et al., 2012; BOSCOLO et al., 2013), but there is a lack of
studies in a polyculture system.
Small-scale farmers dominate
the agriculture landscape throughout Brazil, particularly in the south region.
For a small fish farmer to convert to organic system many elements need to be
accomplished and a range of different organic management models can be defined.
The aim of this study is to contribute to determine one model by verifying the
performance of fishes fed with organic artisanal and conventional commercial
diets in a polyculture system.
MATERIAL E METHODS
This research was conducted
from November 2014 to November 2015 (352 days) in four small-scale producers
located in the state of Paraná, southern Brazil. In each small farm, two
earthen ponds (size varying from 200 to 500 m2) were managed
following the Brazilian organic aquaculture legislation IN 28/2011 (BRASIL,
2011). Agricultural limestone and organic fertilizer in the form of chicken
dung were spread in dry form on the bottom of the fishponds at the rate of 100g
m-2 one week prior filling up to 1.5 m depth. Subsequently, the
water level was maintained through fortnight compensation of about 4–6 cm of
seepage and evaporation loss. Considering an organic model, three neotropical
native species were combine with cyprinid fishes in order to established the
following experimental polyculture system: silver catfish R. quelen (30% of the individuals; 0.23 g initial weight),
common carp C. carpio (20%; 0.55 g), armored catfish Pterygoplichthys joselimaianus
(15%; 1.04 g), curimba Prochilodus
lineatus (15%; 5.19 g), silver carp H.
molitrix (7,5%; 1.10 g), bighead carp H. nobilis
(7,5%; 14.57 g) and grass carp C. idella (5%;
0.59 g). Fingerlings were purchased from a commercial hatchery and stocked at a
total density of 1.5 fish m-2.
A complete randomized block
experimental design was used, in which each of four small farmers individually
was considered a block with two ponds, where fish was fed pelleted Organic
artisanal diet (Organic) and extruded conventional Commercial diet
(Commercial). Each pond was considered a replicate (n=4). Crude protein
concentration (CP) and particle size of the diets and feeding rates were the
same for both Organic and Commercial treatments and varied during the culture
period (Table 1). Feeding rates (% of biomass) were adjusted considering R. quelen and common carp growth measured through
intermittent sampling every 60-90 days.
Table 1. Crude protein (%) and particle size of Organic and Commercial diets
and feeding rate for 352 days experimental growth period. |
||||
Period of
growth |
Number of days |
Feed and Feeding Regime |
||
Crude protein (%) |
Particle size |
Feeding Rate (% of biomass)* |
||
November 2014 – January 2015 |
90 |
40 |
Powder |
10 |
February – August 2015 |
210 |
36 |
3 mm |
3 |
September - November 2015 |
52 |
32 |
5 mm |
2 |
*Considering only
the biomass of the two main species (R. quelen
and C. carpio).
Organic diets were prepared
with fishmeal, mineral/vitamin premix and certified organic ingredients and
three levels of crude protein (Table 2). Ingredients were weighted,
homogenized, mixed, moistened and pelleted. Then, each diet was dried using a
forced ventilation oven at 45oC for 24h and packed to use in each
producer. Fish were fed once daily six days per week.
The commercial fish diets were
purchased at a local store. The levels of guarantee from the manufacturer are
presented in table 3.
Water quality was monitored
every month during experimental period. The abiotic variables water temperature
(oC), pH, dissolved oxygen (mg L-1),
electric conductivity (μS cm-1) and water
transparency (cm) were measured in the field using standard electrodes of
multiparameter probe (Horiba U-50, Kyoto, Japan) and, in the latter case, a
Secchi disk. Total alkalinity (mg CaCO 3 L-1)
and total hardness (mg CaCO 3 L-1) were
performed with colorimetric tests using an Aquaculture Kit from February to
October 2015. Samples were obtained at a depth of 30 cm in ponds on the same
sampling day and transported under refrigeration to the laboratory, where the analyses
of nitrogenous and phosphorus compounds (mg L-1) were conducted.
Total N (TN) and total P (TP) were measured according to Valderrama (1981), from
unfiltered water samples. Ammonium (N-NH 4+) was determined from
filtered water samples, following Solorzano (1969).
Table 2. Ingredients and composition of the Organic diets (%
dry matter). |
|||
Ingredients |
Diets (% Crude Protein) |
||
40 |
36 |
32 |
|
Fish meal |
24 |
20 |
17 |
Soybean meal |
44 |
36.6 |
33 |
Wheat flour |
6 |
15.5 |
8.6 |
Maize |
21 |
25.2 |
36.9 |
Soybean oil |
3 |
1.2 |
1 |
Salt |
0.5 |
0.5 |
0.5 |
Premix1 |
1.5 |
1 |
2 |
Dicalcium phosphate |
0 |
0 |
1 |
Proximate composition |
|
|
|
90 |
90 |
90 |
|
Crude fat (%) |
11.0 |
8.7 |
8.1 |
Ash (%) |
10.2 |
9.0 |
9.4 |
Fiber (%) |
3.6 |
4.0 |
3.4 |
NFE (%)2
|
35.0 |
42.3 |
46.5 |
Digestible energy (kcal/kg)3 |
3610 |
3400 |
3230 |
1Composition – units/kg
of premix: antioxidant 0.6 g; folic acid 250 mg; pantothenic acid 5.000 mg; biotin 125 mg; niacin 5,000 mg; vitamin A
1,000,000 IU; thiamine 1.250 mg; cyanocobalamin 3.750 mg; riboflavin
2.500 mg; pyridoxine 2.485 mg; ascorbic
acid 42.000 mg; vitamin
D3 500,000 IU; vitamin E 20,000 IU; vitamin K3 500 mg; cobalt 25
mg; copper 2.000 mg; iron
13,820 mg; iodine 100 mg; manganese
50 mg; selenium 75 mg and
zinc 17.500 mg. 2 Nitrogen
free extract (Digestible carbohydrates) = 100
– (ash + fat + crude protein + fiber). 3 Digestible energy = (5.64 cal g-1 x %CP x 0.9) + (9.51 cal g-1 x %fat x 0.85) + (4.11 cal g-1 x % carbohydrates x 0.5) (JOBLING,
1983). |
Table 3. Composition of the Commercial diets (% dry matter),
levels of guarantee from the manufacturer. |
||||
Proximate composition |
Diets (% Crude Protein) |
|||
40 |
36 |
32 |
||
Dry matter (%) |
90 |
90 |
90 |
|
Crude fat (%)
minimum |
4 |
4 |
4 |
|
Ash (%) maximum |
10 |
10 |
10 |
|
Fiber (%) maximum |
5 |
5 |
5 |
|
At the end of the experiment,
fishes were harvested by repeated netting and finally by total draining of
ponds for complete fish removal. Each species was individually counted to
record biometrical measures and calculate survival rates and growth parameters
– Survival (%); Final Weight (g); Specific Growth Rate – SGR (% day-1)=
100*(Ln final weight – Ln initial weight)/days of culture), Condition Factor –
K (g cm-3)= 100*(wet weight/length3) and Final Biomass –
FB (kg ha-1). The feed conversion ratio – FCR was calculated
considering the sum of the feed weight provided to each system and the biomass
production of the two main species (i.e. R. quelen
and C. carpio). As a matter of fact, the
weight gain of those main species were the only ones considered for the feeding
rate. In addition, at the end of the experiment, samples of three R. quelen and three C. carpio
were randomly collected from each pond, euthanized with anaesthetic
overdose (clove oil, 400 mg L-1) and stored at -20 °C until analysis
to determine the fillet composition. The fillets obtained from the three
sampled fish of each species per replicate (n=12) were minced and homogenized
for analysis following standard procedures (AOAC, 2000). Dry matter was
obtained through drying samples at 105 oC,
ash by incineration at 550 oC, fat by
ether extraction and crude protein by Kjeldahl method
(N x 6.25). Data from the feeding trial, fish filet composition and water
quality parameters were compared by using Student ́s t test.
RESULTS AND DISCUSSION
The results of final biomass,
survival for all species and feed conversion ratio of R. quelen
and C. carpio are shown in Table 4. Final
biomass was significantly higher (P < 0.05) in ponds fed with Organic
diet (4,877.8 kg ha-1) than in the Commercial diet treatment
(3,067.1 kg ha-1). Also, feed conversion ratio for both main species
(R. quelen
+ C. carpio)
was significantly better for Organic treatment. On the other hand, total final
survival did not differ between treatments.
Table 4. Final biomass,
survival and feed conversion ratio for Organic and Commercial treatments, at
the end of 352 days experimental growth period. |
|||
Treatments |
Final biomass (kg ha-1) |
Survival (%) |
FCR (R. quelen + C. carpio) |
Organic |
4,877.8 ±
1,044.9a |
63.2 ± 10.9 |
1.2 ± 0.1a |
Commercial |
3,067.12 ± 483.5b |
57.4
± 2.9 |
1.6
± 0.1b |
P value Student t test |
0.020 |
0.730 |
0.009 |
Different superscript letters
in the same column indicate statistical difference between treatments (P<0.05);
values are expressed as mean±SD (n=4). |
Final biomass can be
considered high for both treatments even though the survival rates were
relatively low. In a similar polyculture system, where fishes were fed
commercial diet, fresh grass and ground corn for seven months, final biomass of
3,198 kg ha-1 and survival rates above 83% were obtained (BARCELOS
et al., 2012). In the present study, final biomass was 59% superior in fish fed
with Organic diet treatment in comparison to Commercial treatment. Despite
total survival rates were not different, individually C. carpio fed organic diet presented
higher rate and as a main specie in the polyculture, representing 20% of the
species, could explain the higher biomass in organic feed treatment. In
addition, the common carp bottom dwelling habit (MATSUZAKI et al., 2009) also favoured sinking (organic) feed intake. Numerically, the
main species (C. carpio
and R. quelen)
had a higher final weight, although no effects were observed among treatments.
Similar results also was observed for anther silver catfish species Rhamdia voulezi fed
organic certified diet when compared to conventional feeding practices, but in
net-cages system for 78 days (FEIDEN et al., 2010).
The survival of both
treatments can be considered less than within the desired range of 75–85% for
earthen ponds in semi intensive systems, and it was clearly influenced by the
low survival of the P. joselimaianus (30%). There is a lack of studies focusing
on fish fed with organic diets. The scarce literature is comprised of studies
carried out over a short period of time and under controlled experimental
conditions, which makes it difficult to compare with our results.
Figure 1. Survival rates for
individual species fed Organic and Commercial diet, at the end of 352 days experimental period.
Different letter
above columns for the same specie indicates statistical difference between
treatments (P<0.05; Student t test). Values are expressed as mean±SD (n=4).
The survival rate of C. carpio and C. idella when analysed
individually, was affected (P<0.05) by treatment (Figure 1). C. carpio fed
organic diet presented higher survival rate when compared to those fed
Commercial diet. In contrast, C. idella fed Organic diet presented lower survival rate
when compared to fish fed Commercial diet, but as the percentage of this specie
was very low in the polyculture (5%) it did not affect the final biomass
results. The variability of survival for individual species ranged from 30.7%
for P. joselimaianus
to 81% for C. carpio
in Organic treatment and from 31.3% for P.
joselimaianus to 84% for H. molitrix in Commercial treatment.
The initial weight of each
fish species used in the polyculture system was similar and, after the 352 days
feeding trial, there was no significant difference between treatments for final
weight, specific growth rate and condition factor as shown in Table 5.
R. quelen and common carp fillet composition are summarized in
Table 6. Moisture, protein, fat and ash were not influenced (P>0.05)
by the type of diet.
Table 5. Final weight, specific growth rate (SGR) and
condition factor (K) for species under Organic and Commercial diet treatments
at the end of the 352 days experimental
growth period1. |
|
|
|
|||||
|
Species2 |
Diets |
P value Student t test |
|
|
|
|
|
|
Organic |
Commercial |
|
|||||
Final weight (g) |
R. quelen |
489.08 ± 118.46 |
341.21 ± 83.63 |
0.088 |
|
|
|
|
|
C. carpio |
784.77 ± 306.52 |
660.28 ± 205.90 |
0.525 |
|
|
|
|
|
P. joselimaianus |
248.71 ± 205.70 |
124.24 ± 25.44 |
0.699 |
|
|
|
|
|
P. lineatus |
269.31 ± 60.83 |
247.32 ± 89.53 |
0.699 |
|
|
|
|
|
H. molitrix |
320.08 ± 95.40 |
207.42 ± 36.53 |
0.070 |
|
|
|
|
|
H. nobilis |
414.16 ± 166.74 |
244.11 ± 103.85 |
0.134 |
|
|
|
|
|
C.idella |
669.94 ± 188.88 |
483.37 ± 234.72 |
0.262 |
|
|
|
|
SGR (% day-1) |
R. quelen |
2.18 ± 0.08 |
2.02 ± 0.07 |
0.102 |
|
|
|
|
|
C. carpio |
2.06 ± 0.10 |
2.02 ± 0.10 |
0.524 |
|
|
|
|
|
P. joselimaianus |
1.48 ± 0.27 |
1.36 ± 0.06 |
0.449 |
|
|
|
|
|
P. lineatus |
1.12 ± 0.07 |
1.09 ± 0.10 |
0.616 |
|
|
|
|
|
H. molitrix |
1.61 ± 0.10 |
1.49 ± 0.05 |
0.079 |
|
|
|
|
|
H. nobilis |
0.94 ± 0.10 |
0.79 ± 0.11 |
0.088 |
|
|
|
|
|
C. idella |
2.00 ± 0.07 |
1.88 ± 0.16 |
0.239 |
|
|
|
|
K |
R. quelen |
1.31 ± 0.10 |
1.25 ± 0.09 |
0.425 |
|
|
|
|
|
C. carpio |
2.18 ± 0.25 |
2.21 ± 0.38 |
0.490 |
|
|
|
|
1Values are expressed as mean±SD
(n=4). 2Rhamdia quelen, Cyprinus carpio, Pterygoplichthys joselimaianus,
Prochilodus lineatus, Hypophthalmichthys molitrix, Hypophthalmichthys
nobilis, Ctenopharyngodon
Idella |
Table 6. Fillet proximal composition (wet basis) of Rhamdia quelen and Cyprinus
carpio fed Organic and Commercial diet, at the
end of the 352 days experimental growth period. |
|
|
|||||
Species |
Treatment |
Moisture
(%) |
Protein (%) |
Fat
(%) |
Ash (%) |
||
R. quelen |
Organic |
73.22 ± 1.88 |
17.95 ± 0.86 |
10.22 ± 1.56 |
1.07 ± 0.02 |
||
|
Commercial |
73.80 ± 2.89 |
18.10 ± 1.12 |
8.19 ± 2.77 |
1.06 ± 0.06 |
||
C. carpio |
Organic |
73.57 ± 2.36 |
17.41 ± 1.22 |
8.98 ± 3.20 |
1.03 ± 0.04 |
||
|
Commercial |
74.93 ± 1.43 |
18.51 ± 1.32 |
7.91 ± 1.12 |
0.93 ± 0.04 |
||
Values are expressed as mean±SD.
Means of pooled samples of three fish from each of four replicate groups. |
|||||||
Few data on the quality of
organically reared fish meat are available. Nutritional characteristics of fish
meat are dependent on chemical composition and can be influenced by the food
consumed (GRIGORAKIS, 2007; CORRÊA et al., 2013). In the present study,
proximate analysis showed that fillet composition was similar for fish fed with
Organic and Commercial diets. In the same way, other fish species such as
European sea bass (Dicentrarchus labrax) (TROCINO et al., 2012); Rhamdia
voulezi, Nile tilapia (Oreochromis niloticus) and Piaractus
mesopotamicus (BOSCOLO et al., 2013) also
presented no differences for moisture, protein, fat and ash levels in the
fillet of fishes fed organic or commercial diets.
Mean values and ranges of
water quality parameters measured during trial are presented in Table 7.
Table 7. Water quality
parameters for Organic and Commercial diet
treatments, during the 352 days experimental
growth period. |
|||
Water quality parameters |
Treatment |
P value Student t
test |
|
Organic |
Commercial |
||
Water temperature (oC) |
22.2 ± 3.1 |
22.3 ± 3.2 |
0.852 |
Transparency (cm) |
30.9 ± 32.7 |
32.5 ± 27.1 |
0.809 |
Alkalinity (mg CaCO3 L-1) |
26.8 ± 8.7 |
30.3 ± 9.1 |
0.176 |
Total hardness (mg CaCO3 L-1) |
30.8 ± 9.3 |
30.4 ± 9.2 |
0.878 |
pH |
6.7 ± 0.9 |
6.7 ± 1.0 |
0.821 |
Electric conductivity (mS cm-1) |
0.07 ± 0.04 |
0.06 ± 0.04 |
0.648 |
Dissolved oxygen – DO (mg L-1) |
6.2 ± 2.1 |
5.5 ± 2.5 |
0.133 |
Total Nitrogen - TN (mg L-1) |
0.275 ± 0.189a |
0.368 ± 0.25b |
0.055 |
Total Phosphorus - TP (mg L-1) |
0.071 ± 0.055 |
0.081 ± 0.092 |
0.546 |
Ammonium - NH4+ (mg L-1) |
0.060 ± 0.036 |
0.082 ± 0.085 |
0.121 |
Values are expressed as mean±SD.
Different superscript letters in the same line indicate statistical
difference between treatments (P<0.05) |
The mean values of alkalinity
and total hardness were similar between treatments as well as to water
temperature, water transparency, pH and electric conductivity. However, both in
Organic and Commercial treatments, lower temperatures were recorded during the
dry season months (April to August), transparency of water presented higher
values at the beginning of the experiment (November and December), and the pH
decreased towards final months of experimental period, which also occurred with
electric conductivity. Dissolved oxygen did not differ statistically between
treatments and was within acceptable limits. Total nitrogen was affected by
treatment (P<0.05) and was higher in treatment with commercial diet
in all experimental period.
Water quality parameters were
within acceptable values for water ponds used in fish culture, despite
alkalinity levels were considered low, but not enough to affect the primary
production of the pond (BRASIL, 2005; BOYD; TUCKER, 1998; KUBITZA, 20118). The
results of the nitrogen compounds, especially Total nitrogen, suggest that
pelleted organic diet was superior to extruded commercial diet in maintaining a
good water quality. Total phosphorus also pointed out better trophic conditions
in organic system due to the tendency to reduce concentrations at the end of
experiment when compared with the commercial system. Values of Ammonium and
Total phosphorus in this experiment were lower than those reported by Dieterich
et al. (2012) of 0,33 mg.L-1 e 0,27 mg.L-1 respectively, in tilapia culture
system fed diets with organic ingredients.
In fish farming, nutrient ions
are mainly from feeding and can trigger eutrophication process that negatively
affects the water quality and consequently the growth and well-being of fishes
(ABU-ELALA al., 2016; CHEZHIAN et al. 2012). In this experiment, the lower
final nitrogen and phosphorus concentrations in water indicates that the organic
diet probably allows better utilization of the feed nutrients by fishes
decreasing possible remains in the cultivation environment and greater recycle
of these nutrients. Thus, in addition to the direct benefits to fish production,
the organic system can contribute to the maintenance of better water quality, with
less susceptibility to occurrence of problems arising from eutrophication, such
as blooms of toxic cyanobacteria and anoxia, therefore more compatibility with
the bases of sustainable aquaculture.
CONCLUSIONS
The poly cultured fish species fed organic
diets has higher performance when comparing to commercial diets. This study
contributed to determine a model of organic fish farming in a polyculture
system, using omnivorous silver catfish, bottom feeder common carp, grass and
plankton-feeders carps.
ACKNOWLEDGMENTS
To the National
Council for Scientific and Technological Development (CNPq,
Brazil) for financial support through the Nucleus of Aquaculture with agroecological
approach- AquaNEA (CNPq
487612/2013-2) and to the Universidade Federal da Fronteira Sul (campus Laranjeiras
do Sul, PR), Universidade Tecnológica
Federal do Paraná (campus Dois Vizinhos,
PR) and to the farmers that generously shared their ponds, time and experience.
REFERENCES
Abu-Elala, N. M.; Abd-Elsalam, R. M.; Marouf, S.;
Abdelaziz, M.; Moustafa, M. Eutrophication, ammonia intoxication, and
infectious diseases: interdisciplinary factors of mass mortalities in cultured
Nile tilapia. Journal of aquatic animal health, v. 28, n. 3, p. 187-198, 2016. 10.1080/08997659.2016.1185050.
AOAC - Association of Official
Analytical Chemists. Official Methods of Analysis. 17 th
ed. Association of Official Analytical Chemists, Gaithersburg, MD, USA. 2000.
1115p.
Barcelos,
L. J. G.; Quevedo, M. R.; Kreutz, L. C.; Ritter, F.; Pandolfo, A.; Hemkemeier,
M.; Colla, L.; SILVA, L. B.; KOAKOSKI, G.; ROSA, J. G. S. Comparative
Analysis of Different Fish Polyculture Systems. Journal of the World
Aquaculture Society, 43(6): 778-789, 2012. 10.1111/j.1749-7345.2012.00613.x.
Beg,
M.M.; Mandal, B.; Moulick, S.; Mukherjee, C. K.; Mal, B.C. Efficacy of organic
fish farming for sustainability. International Journal of Advanced Biological Research, v. 6, n. 2, p. 180-187, 2016.
Boscolo, W.R; Neu, D.H.; Klein, S.; Sary, C.; Feiden,
A.; Camargo, Fernandes, D.R.A. Ração
orgânica na dieta de três espécies de peixes: desempenho, rendimento de carcaça
e composição centesimal de jundiás (Rhamdia
voulezi), tilápias (Oreochromis
niloticus) e pacu (Piaractus
mesopotamicus) criados em tanques rede. Cultivando o Saber, v. 6,
n.3, p. 40-53, 2013.
BOYD, C. E.; TUCKER, C. S.
Ponds Aquaculture Water Quality Management. New York: Springer Science &
Business Media, 1998. 700 p.
BRASIL,
Instrução Normativa Interministerial 28 de 8 de junho de 2011. <http://www.normaslegais.com.br/legislacao/in_mapa_mpa28_2011.htm> . Accessed 28 June 2019.
BRASIL.
Ministério do Meio Ambiente. Conselho Nacional do Meio Ambiente. Resolução
Conama no 357, de 17 de março de 2005. <http://www2.mma.gov.br/port/conama/legiabre.cfm?codlegi=459.> Accessed 28
June 2019.
Chezhian
A., Senthamilselvan D., Kabilan N. Histological changes induced by ammonia and pH on
the gills of fresh water fish Cyprinus carpio
var. communis (Linnaeus). Asian Journal of
Animal Veterinary Advances, v. 7, n. 7, p. 588-596, 2012. 10.3923/ajava.2012.588.596.
Corrêa, C. F.; Tachibana, L.; Leonardo, A. F.;
Baccarin, A. E. Rendimento de carcaça,
composição do filé e análise sensorial do robalo-peva de rio e de mar. Boletim do Instituto de Pesca, v. 39, n. 4, p. 401-410, 2013.
SILVA L. B.; BARCELLOS, L. J.
G.; QUEVEDO, R. M.; SOUZA, S. M. G.; KESSLER, A. M.;KREUTZ, L. C.; RITTER, F.;
FINCO, J. A.; BEDIN, A. C. Introduction of jundia Rhamdia quelen (Quoy & Gaimard) and Nile tilapiaOreochromis niloticus
(Linnaeus) increases the productivity of carp polyculture in southern Brazil. Aquaculture Research, v. 39, n. 5,
p.542-551, 2008. 10.1111/j.1365-2109.2008.01912.x
Dieterich, F.; Boscolo, W. R.; Losch, J. A.; FEIDEN, A.; FURUYA, W. M.; SIGNOR, A. A. Fontes de
fósforo em rações orgânicas para alevinos e juvenis de tilápia-do-nilo. Pesquisa Agropecuária Brasileira, v. 47, n. 3, p.
417-424, 2012.
FAO
Food and agriculture organization. The state of world fisheries and aquaculture
2016 - contributing to food security and nutrition for all Rome: FAO, 2016. 200
p.
FEIDEN,
A.; SIGNOR, A. A.; DIEMER, O. et al. Desempenho
de juvenis de jundiás (Rhamdia voulezi) submetidos à alimentação com ração orgânica
certificada e comercial. Revista Acadêmica: Ciências Agrárias e Ambientais, v. 8,
n.4, p. 381-387, 2010.
Gentelini, A. L. Gomes, S. D.; Feiden, A.; ZENATTI, D.; SAMPAIO, S. C.; COLDEBELLA, A.Produção de biomassa das macrófitas aquáticas Eichhornia crassipes
(aguapé) e Egeria densa (egeria)
em sistema de tratamento de efluente de piscicultura orgânica. Semina: Ciências Agrárias, Londrina, v.
29, n. 2, p. 441-448, 2008. 10.5433/1679-0359.2008v29n2p441.
Grigorakis, K. Compositional
and organoleptic quality of farmed and wild gilthead sea bream (Sparus aurata) and sea bass (Dicentrarchus
labrax) and factors affecting it: a review.
Aquaculture, v. 272, n. 1-4, p. 55-75, 2007. 10.1016/j.aquaculture.2007.04.062.
Hao-Ren, L. Polyculture
systems of freshwater fish in China. Canadian Journal of Fisheries and Aquatic
Sciences, v. 39, p. 143–50, 1982. 10.1139/f82-015.
HernÁndez,
M.; Gasca-Leyva, E.; Gressler, P., D.; Krise, D. Effects of farm and
commercial inputs on carp polyculture performance: participatory trial in an
experimental field station. Latin American Journal of Aquatic Research, v. 42,
n. 3), p. 468-476, 2014. 10.3856/vol42-issue3-fulltext-7.
KUBITZA,
F. Tilápia: tecnologia e planejamento na produção comercial. 2. ed. Jundiaí: F. Kubitza, 2011. 316 p.
Paul,
B. G.; Vogl, C. R. Organic shrimp aquaculture for sustainable household livelihoods in
Bangladesh. Ocean & Coastal Management, v. 71, p. 1-12. 2013. 10.1016/j.ocecoaman.2012.10.007.
Solorzano,
L. Determination
of ammonia in natural waters by the phenolhypochlorite
method. Limnology and Oceanography, v. 14, p. 799-801, 1969. 10.4319/lo.1969.14.5.0799.
Trocino,
A.; Xiccato, G.; Majolini, D.; TAZZOLI, M.; BERTOTTO, D.; PASCOLI, F.; PALAZZI, R.
Assessing the quality of organic and conventionally-farmed European sea bass (Dicentrarchus labrax).
Food Chemistry, v. 131, p. 427–433, 2012. 10.1016/j.foodchem.2011.08.082.
Valderrama,
J. C. The
simultaneous analysis of nitrogen and total phosphorus in natural waters.
Marine Chemistry, v. 10, p. 109-122, 1981. 10.1016/0304-4203(81)90027-X.