Printer Friendly

Accidentally catching of the catfish Lophiosilurus alexandri (Steindachner, 1876) larvae in aquariums with different colors/ Interferencia de cores de aquarios nas larvas do bagre Lophiosilurus alexandri (Steindachner, 1876) e seu tratador.

1. Introduction

The pacama Lophiosilurus alexandri, Steindachner, 1876 (Siluriformes: Pseudopimelodidae) is an important species of commercial freshwater aquaculture (Pedreira et al., 2012), endemic of the Sao Francisco Basin, with a great importance for fishing. Such features have encouraged studies of larval rearing (Pedreira et al., 2012; Costa et al., 2017), morphology (Guimaraes-Cruz et al., 2009; Mello et al., 2015) and restocking programs.

Fish larvae are visual predators, and development and survival can be influenced by contrast, luminosity (Pedreira, 2001; Pedreira et al., 2012), photoperiod (Villamizar et al., 2009), turbidity (Ohata et al., 2011) and color (Pedreira, 2001; Pedreira et al., 2012; Costa et al., 2013). In addition to the visual capacity of Siluriformes, such as L. alexandri, the sensorial capacity is provided with wattles and lateral line, and fish perceive changes in water currents caused by prey, conspecifics and predators in the environmental (Rodrigues-Galdino et al., 2009).

An escape response is a rapid maneuver used by fish larvae to escape predators (Nair et al., 2017). In this case, those who perform the daily cleaning of the facilities, a maneuver in a favorable direction, or from a longer distance, has the chance to improve the survival of the larva, being an unpredictable behavioral behavior to be evaluated. Therefore, the survival of the prey depends on the kinematics of the escape and who performs the management. Fish larvae have a remarkable ability to sense and escape an attack from a larger predator (Stewart et al., 2014). Despite the importance of these events for fish biology, it is not clear how sensory cues stimulate effective evasive maneuvering.

Therefore, this experiment aimed to evaluate the effect of different aquariums colors in the development and survival of L. alexandri larvae, as well it influence over the visual ability of the handler during the handling routine.

2. Material and Methods

The experiment was conducted at Federal University of the Valley of Jequitinhonha and Mucuri--UFVJM in Diamantina--MG, Brasil, during 12 days, in December, 2016. Six hundred forty L. alexandri larvae, from the same batch, with 1.28 [+ or -] 0.05 cm and 29 [+ or -] 3.0 mg, of total length and weight, respectively were distributed with 5 L-aquariums, at density of 7 larvae [L.sup.-1] (40 larvae [aquarium.sup.-1]).

The treatments consisted of the use of aquariums with different colors (all the wall), as follows: two bright colors (green and blue) and two dark colors (brown and black), with four replications each.

Each larva receives 600Artemia sp. (Pilla and Beardmore, 1994) nauplii [daily.sup.-1] (estimation) offered twice [day.sup.-1], at 8 am and 2 pm. On the sixth day the amount of Artemia sp. nauplii was increased, and each larva receives 1.200 [daily.sup.-1].

Artemia sp. cysts were kept for 24 h in 28.5 %o--salinized water, until they hatch. After hatching the nauplii were counted under a stereoscopic for checking the nauplii [mL.sup.-1] density, and thus determined the feeding volume for larvae. Every day at 8 am, water temperature ([degrees]C), pH, oxireduction potential (ORP), and dissolved oxygen (mg [L.sup.-1] and %--saturation) of each aquarium were measured. After the measurement of the limnological variables, the aquariums were cleaned below a luminosity of [greater than or equal to] 1470 lux, for the waste removal, and 10%--water volume was exchange.

Daily, the dead larvae were counted and removed, and the survival was calculated from the start until the finish of the experiment, to obtain the mean number of dead larvae during its first days, for all treatments together. Also, daily the number of accidentally captured larvae, with motility, during cleaning was counted. These counts had the purpose to analyzing the degree of the interference of the aquarium color in the visual perception of the handler. The recovered larvae was the count of the total larvae at the beginning to the end of the experiment., and the daily recovered larvae was the total larvae count, divided by the total number of days (12 days).

Larvae were subjected to natural photoperiod with a light intensity of 330.6 [+ or -] 39.51 lux. A Minolta CR400 colorimeter was used to measure color and lightness of aquariums. The colors were expressed in CIELab coordinates. In this system, [L.sup.*] represents the lightness of color points on a 0-100 scale from black to white, [a.sup.*] is the position between red (+) and green (-), while [b.sup.*] is the position between yellow (+) and blue (-), and thus, [a.sup.*] and [b.sup.*] are chromaticity coordinates.

Immediately at the end of the experiment, all larvae were counted individually, and biomass was obtained by weighing all larvae (pool) of each repetition in the same time, in analytical balance (0.1 mg accuracy). The total and standard lengths and weight were measured with a caliper (0.02 mm precision) and analytical balance, respectively.

The aquariums colors data, the limnological parameters, and the effect of the aquariums colors on development and survival of larvae, and the handler visualization were compared by ANOVA and Tukey test at 0.05 significance using SigmaStat 3.5 program.

3. Results

Water variables did not differ between the aquariums colors (see in Table 1).

The color intensity was different among the colorful aquariums (as shown in Table 2), it influenced handler's ability to detect larvae but did not affect the L. alexandri larvae survival and growth development (as observed in Table 3).

The plato quadratic regression shows that mortalities was low, without effect (see in Figure 1).

4. Discussion

Water limnological variables did not differ among the different aquarium colors, demonstrating that the coloration did not affect the water quality, as found by Pedreira et al. (2012) and Costa et al. (2017). The water parameters of this study were within the favorable range for cultivation of the species, as well as described by Pedreira et al. (2012).

The color intensity was different between the colorful aquariums, which was expected, but did not influence the L. alexandri larvae survival, similarly observed by Pedreira et al. (2012) and for juveniles by Costa et al. (2017). The aquarium with different colors did not influence the catfish larvae development, as observed by Costa et al. (2017) for juveniles of the same species. Pedreira et al. (2012) verified that L. alexandri larvae ingested the same number of prey and efficiently, when submitted to aquariums with different colors. These results can be explained by the greater plasticity presented by freshwater fishes that are adapted to unstable environments (Vera et al., 2009). Yang et al. (2013) also verified the catfish's ability to tolerate environmental variation.

Pedreira et al. (2012) described that the brown and black colored aquariums favors higher weight and length gain for L. alexandri larvae. The better development for L. alexandri larvae was due to the association between the color of the aquarium and the benthic habitat of specie. In general, African catfish Clarias gariepinus have higher survival rates in the dark conditions, when larvae have a greater swimming activity and also a significantly aggressive behavior decrease (Mukai et al., 2013). Catfish usually have benthic and nocturnal habits, although many species are active during the day, especially in turbid waters (Dantas et al., 2016). African catfish larvae, C. gariepinus, subjected to total darkness have a higher survival and biomass (Adewolu et al., 2008). In the darkness environment there was a decrease in energy expenditure of locomotor activity, cannibalism, metabolism and energy canalization for the weight gain of African catfish (Appelbaum and Kamler, 2000).

The L. alexandri larvae visual perception as well as for other Siluriformes is an important tool, but not so prominently as to Characiformes (Pedreira et al., 2012). The L. alexandri larvae have a similar development in bright and dark aquariums, demonstrating that the perception of prey by neotropical Siluriformes larvae in low light environments. It can be attributed to the visual and chemical perception, as observed for the channel catfish, Ictalurus punctatus (Rafinesque, 1818) (Valentincic and Caprio, 1994), and also the mechanical perception, as verified for the jundia Rhamdia quelen (Quoy and Gaimard, 1824) (Rodrigues-Galdino et al., 2009).

An escape response is a fish larvae behavior to escape predators (Nair et al., 2017), and the handler during daily management plays the role of predator, promoting stress in the larvae, due to the lack of visualization and scape capacity of the animal due to low development. Therefore, the survival of the prey depends on the escape kinematics and who performs the management. Although fish larvae have a remarkable ability to sense and escape an attack from a larger predator (Stewart et al., 2014), the leakage does not reduce mortality (Nair et al., 2017), however an environment with easier observation for management allows to avoid the larval accidental capture. Despite the importance of these events for fish biology, it is not clear how sensory cues stimulate effective evasive maneuvering.

In the present experiment, black aquariums had a higher number of recovered L. alexandri larvae during daily handling, indicating the handler visualizing difficulty, causing stress for catfish larvae during the cleaning of the aquarium. This befell because the dark dorsum of the larvae did not allow the handler to distinguish the aquarium background and larvae. Pedreira (2001) described that aquariums with dark background difficult the handler perception of larvae and waste remove, damaging cleaning and resulting in the water quality deterioration, which in intensive rearing, adversely affects the yield and may even determine high rates of mortality.

Looking at the figure of mortality in the first days of life, it is possible to verify that between the second and third day occur the greatest larvae mortalities, regardless of treatment. In this same figure it is possible to visualize the number of accidentally captured larvae, and this assumes that the high mortality in early larval life was not influenced by the handler management, but due to the fragility of the larvae in the first days of life (Lucas and Southgate, 2003). According to the results of the plateau regression the mortality was insignificant, again confirming that the type of management did not influence the stress of pacama larvae.

Despite the vision is generally considered the dominant human sensory modality; self-contained and independent of other senses (Shams and Kim, 2010), the literature is scarce on the interference of the aquariums colors on the handler viewing in the freshwater fish breeding. According to researches, the color is important in human visual perception, depending on it contrast with nearby surfaces, may increase or decrease the observation efficiency (Cornelissen et al., 2006) and consequently of work (Vladusich et al., 2007), as perceived in L. alexandrilarviculture. Thus, adjustments in the management provide better handling of L. alexandri larvae, and facilitate the daily handling decreasing stress, being an important influence in fish production system (Pedreira, 2001).

At last, this study highlights the interference of aquarium color on pacama larvae during handling, and recommends aquariums colors that provide contrast with the L. alexandri larvae, facilitating the handler visualization, as suggested by Pedreira (2001), once do not impaired the survivorship and development of larvae. Black aquariums are not recommended for L. alexandri growing, because during cleaning, the handler almost can't see the larvae, due to the dark dorsum, and may consequently hurting or killing the larvae.

The catfish L. alexandri larvae should be cultivated in aquariums that allow a good contrast among the larvae and the background, to avoid accidental capture of larvae by the handler. It is suggested to avoid the use of dark and black aquariums.


FAPEMIG, BNB, CAPES and CNPq for financial support, and CODEVASF by providing biological material.


ADEWOLU, M.A., OGUNSANMI, A.O. and YUNUSA, A., 2008. Studies on growth performance and feed utilization of two Clarias catfish and their hybrid reared under different culture systems. European Journal of Scientific Research, vol. 23, no. 2, pp. 252-260.

APPELBAUM, S. and KAMLER, E., 2000. Survival, growth, metabolism and behavior of Clarias gariepinus (Burchell, 1822) early stages under different light conditions. Aquacultural Engineering, vol. 22, no. 4, pp. 269-287. S0144-8609(00)00054-6.

CORNELISSEN, F.W., WADE, A.R., VLADUSICH, T., DOUGHERTY, R.F. and WANDELL, B.A., 2006. No functional magnetic resonance imaging evidence for brightness and color filling-in in early human visual cortex. The Journal of Neuroscience, vol. 26, no. 14, pp. 3634-3641. JNEUROSCI.4382-05.2006. PMid:16597716.

COSTA, D.C., MARCELO, M.P, CORASPE-AMARAL, M.V., DUPIM, A.E., BARRAL, U. and DUARTE, E., 2013. Larviculture of piabanha-do-pardo in aquariums of different colors. Pesquisa Agropecuaria Brasileira, vol. 48, no. 8, pp. 1005-1011. http://

COSTA, D.C., MATTIOLI, C.C., SILVA, W.S., TAKATA, R., LEME, F.O.P., OLIVEIRA, A.L. and LUZ, R.K., 2017. The effect of environmental color on the growth, metabolism, physiology and skin pigmentation of the carnivorous freshwater catfish Lophiosilurus alexandri. Journal of Fish Biology, vol. 90, no. 3, pp. 922-935. PMid:27981570.

DANTAS, N.C.F.M., SILVA JUNIOR, C.A.B., LIPPI, D.L. and FEITOSA, C.V., 2016. Diel variation and ecological aspects in fish assemblages of Sandy beach in the semi-arid region of northeast Brazil. Brazilian Archives of Biology and Technology, vol. 59, no. 0, pp. 1-11.

GUIMARAES-CRUZ, R.J., SANTOS, J.E., SATO, Y. and VELOSO-JUNIOR, V.C., 2009. Early development stages of the catfish Lophiosilurus alexandri Steindachner, 1877 (Pisces: Pseudopimelodidae) from the Sao Francisco River basin, Brazil. Journal of Applied Ichthyology, vol. 25, no. 3, pp. 321-327. http://

LUCAS, S. J., and SOUTHGATE, P. 2003. Aquaculture: farming aquatic animals and plants. Oxford: Fishing News Book.

MELLO, G.C.G., DOS SANTOS, J.E., GUIMARAES-CRUZ, R.J., GODINHO, A.L. and GODINHO, H.P, 2015. Allometric larval growth of the bottom-dwelling catfish Lophiosilurus alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae). Neotropical Ichthyology, vol. 13, no. 4, pp. 677-684. http://dx.doi. org/10.1590/1982-0224-20140161.

MUKAI, Y., SANUDIN, N., FIRDAUS, R.F. and SAAD, S., 2013. Reduced cannibalistic behavior of African catfish, Clarias gariepinus, larvae under dark and dim conditions. Zoological Science, vol. 30, no. 6, pp. 421-424. zsj.30.421. PMid:23721464.

NAIR, A., NGUYEN, C. and MCHENRY, M.J. 2017. A faster escape does not enhance survival in zebrafish larvae. Royal Society Proceedings B, vol. 284, no. 1852, pp. 1-8. http://dx.doi. org/10.1098/rspb.2017.0359.

OHATA, R., MASUDA, R., UENO, M., FUKUNISHI, Y. and YAMASHITA, Y., 2011. Effects ofturbidity on survival of larval ayu and red sea bream exposed to predation by jack mackerel and moon jellyfish. Fisheries Science, vol. 77, no. 2, pp. 207-215.

PEDREIRA, M.M., 2001. Influencia da cor e da luminosidade no cultivo de larvas de peixes. Panorama da Aquicultura, vol. 7, pp. 43-55.

PEDREIRA, M.M., SAMPAIO, E.V., SANTOS, J.C.E. and PIRES, A.V., 2012. Larviculture oftwo neotropical species with different distributions in the water column in light- and dark-colored tanks. Neotropical Ichthyology, vol. 10, no. 2, pp. 439-444. http://dx.doi. org/10.1590/S1679-62252012005000011.

RODRIGUES-GALDINO, A.M., MAIOLINO, C.V., FORGATI, M., DONATTI, L., MIKOS, J.D., CARNEIRO, P.C. and RIOS, F.S., 2009. Development of the neotropical catfish Rhamdia quelen (Siluriformes, Heptapteridae) incubated in different temperature regimes. Zygote (Cambridge, England), vol. 18, no. 2, pp. 131-144. PMid:19857361.

SHAMS, L. and KIM, R., 2010. Crossmodal influences on visual perception. Physics of Life Reviews, vol. 7, no. 3, pp. 269-284. PMid:20447880.

STEWART, W. J., NAIR, A., JIANG, H. and MCHENRY, M.J., 2014. Prey fish escape by sensing the bow wave of a predator. The Journal of Experimental Biology, vol. 217, no. Pt 24, pp. 4328-4336. PMid:25520384.

VALENTINCIC, T.B. and CAPRIO, J., 1994. Chemical and visual control of feedind and escape behaviors in the channel catfish Ictalurus punctatus. Physiology & Behavior, vol. 55, no. 5, pp. 845-855. PMid:8022904.

VERA, L.M., CAIRNS, L., SANCHEZ-VAZQUEZ, F.J. and MIGAUD, H., 2009. Circadian rhythms of locomotor activity in the Nile Tilapia (Oreochromis niloticus). Chronobiology International, vol. 26, no. 4, pp. 666-681. http://dx.doi. org/10.1080/07420520902926017. PMid:19444748.

VILLAMIZAR, N., GARCIA-ALCAZAR, A. and SANCHEZ-VAZQUEZ, F. J., 2009. Effect of light spectrum and photoperiod on the growth, development and survival of European sea bass (Dicentrarchus labrax) larvae. Aquaculture (Amsterdam, Netherlands), vol. 292, no. 1-2, pp. 80-86. aquaculture.2009.03.045.

VLADUSICH, T., LUCASSEN, M.P and CORNELISSEN, F.W., 2007. Brightness and darkness as perceptual dimension. PLoS Computational Biology, vol. 3, no. 10, pp. 1849-1858. PMid:18237226.

YANG, H., CAO, Z.D. and FU, S.J., 2013. The effects of diel-cycling hypoxia acclimation on the hypoxia tolerance, swimming capacity and growth performance of southern catfish (Silurus meridionalis). Comparative Biochemistry and Physiology. A. Comparative Physiology, vol. 165, no. 2, pp. 131-138. http:// PMid:23474254.

M. M. Pedreira (a), D. C. Costa (a) and M. Schorer (a) *

(a) Laboratorio de Aquicultura e Ecologia Aquatica, Departamento de Zootecnia, Universidade Federal dos Vales do Jequitinhonha e Mucuri--UFVJM, Rodovia MGT 367, Km 583, 5000, Alto da Jacuba, CEP 39i00-000, Diamantina, MG, Brasil

* e-mail:

Received: September 19, 2017--Accepted: February 21, 2018--Distributed: November 30, 2019 (With 1 Figure)

Caption: Figure 1. Graphical representation of the relationship between the mortality of pacama larvae during the days of experimentation for the segmented regression method with quadratic plateau.
Table 1. Mean values ([+ or -] standard deviation) of the
limnological parameters for Lophiosilurus alexandri
larviculture, under different aquariums colors.

Aquarium colors                  Green                   Blue

Temperature               21.50 [+ or -] 1.41     21.44 [+ or -] 1.43
pH                        6.58 [+ or -] 0.28      6.75 [+ or -] 0.33
Oxidoreduction          704.33 [+ or -] 0.71    703.44 [+ or -] 0.88
  potential (mV)
Dissolved oxygen          3.05 [+ or -] 1.36      3.00 [+ or -] 1.49
  (mg [L.sup.-1])
Oxygen saturation (%)    31.58 [+ or -] 16.12    33.79 [+ or -] 15.49

Aquarium colors                  Black                   Brown

Temperature               21.44 [+ or -] 1.51     21.57 [+ or -] 1.43
pH                         6.79 [+ or -] 0.32      6.66 [+ or -] 0.44
Oxidoreduction           703.56 [+ or -] 0.73    704.00 [+ or -] 0.00
  potential (mV)
Dissolved oxygen           2.81 [+ or -] 1.39      3.05 [+ or -] 1.77
  (mg [L.sup.-1])
Oxygen saturation (%)     31.79 [+ or -] 14.67    25.60 [+ or -] 19.48

Mean in the same row, did not differ significantly according
to ANOVA, a 0.05 probability.

Table 2. Mean values ([+ or -] standard deviation) of colors
expressed in CIELab coordinates ([L.sup.*]: lightness;
[a.sup.*]: red when positive, grey when zero and green when
negative; [b.sup.*]: yellow when positive, green when zero
and blue when negative) and reflected luminosity in different
aquariums colors for Lophiosilurus alexandri larviculture.

                                Aquarium colors
variables               Green                     Blue

[L.sup.*]        66.7 [+ or -] 2.08 (b)    56.4 [+ or -] 0.65 (c)
[a.sup.*]       -24.2 [+ or -] 1.42 (d)   -17.3 [+ or -] 0.68 (c)
[b.sup.*]        42.0 [+ or -] 2.78 (a)   -26.0 [+ or -] 4.08 (d)
Reflected        69.4 [+ or -] 6.85 (a)    32.2 [+ or -] 2.65 (b)

                   Aquarium colors
variables               Black

[L.sup.*]       33.6 [+ or -] 1.25 (e)
[a.sup.*]        0.5 [+ or -] 0.22 (b)
[b.sup.*]        0.8 [+ or -] 0.92 (c)
Reflected       19.0 [+ or -] 1.87 (d)

Mean in the same row followed by different letters differed
significantly (p<0.05) by Tukey's test.

Table 3. Mean values ([+ or -] standard deviation) of
Lophiosilurus alexandri larvae development in different
aquariums colors.

                                  Green                   Blue

Survival (%)            50.8 [+ or -] 20.8 (a)   61.7 [+ or -] 13.8 (a)
Total length (mm)       1.98 [+ or -] 0.09 (a)   2.01 [+ or -] 0.08 (a)
Standard length (mm)    1.44 [+ or -] 0.08 (a)   1.46 [+ or -] 0.06 (a)
Weight (mg)             0.06 [+ or -] 0.01 (a)   0.06 [+ or -] 0.01 (a)
Biomass (g)             1.25 [+ or -] 0.64 (a)   1.71 [+ or -] 0.38 (a)
Recovered larvae        1.67 [+ or -] 1.53 (b)   2.00 [+ or -] 1.00 (b)
Daily recovered
  larvae                0.14 [+ or -] 0.39 (b)   0.17 [+ or -] 0.22 (b)

                                  Black                  Brown

Survival (%)            76.7 [+ or -] 18.4 (a)   70.8 [+ or -] 14.2 (a)
Total length (mm)       1.98 [+ or -] 0.10 (a)   2.01 [+ or -] 0.01 (a)
Standard length (mm)    1.44 [+ or -] 0.08 (a)   1.45 [+ or -] 0.09 (a)
Weight (mg)             0.06 [+ or -] 0.01 (a)   0.06 [+ or -] 0.01 (a)
Biomass (g)             0.71 [+ or -] 0.44 (a)   1.71 [+ or -] 0.33 (a)
Recovered larvae        6.33 [+ or -] 2.52 (a)   0.67 [+ or -] 0.58 (b)
Daily recovered
  larvae                0.53 [+ or -] 0.33 (a)   0.06 [+ or -] 0.13 (b)

Mean in the same row followed by different letters differed
significantly (p<0.05) by Tukey's test.
COPYRIGHT 2019 Association of the Brazilian Journal of Biology
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2019 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Original Article
Author:Pedreira, M.M.; Costa, D.C.; Schorer, M.
Publication:Brazilian Journal of Biology
Date:Sep 12, 2019
Previous Article:Parasitoids diversity in organic Sweet Pepper (Capsicum annuum) associated with Basil (Ocimum basilicum) and Marigold (Tagetes erecta)/Diversidade de...
Next Article:Aquatic macrophytes and trophic interactions: a scientometric analyses and research perspectives/Macrofitas aquaticas e interacoes troficas: analise...

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |