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International Journal of Fisheries Science and Research

Effect of Fishmeal Substitution by Lima Bean Meal on the Zoo Technical Performances of African Catfish (Clarias gariepinus) in the Bati

Abstract Citation Introduction Material and Methods Results and Discussion Discussion Conclusion References
Details

Received: 05-Nov-2018

Accepted: 19-Nov-2018

Published: 21-Nov-2018

Emile Miégoué1*, Pégis Davy Tagning Zebaze2, Fernand Tendonkeng1, Lemoufouet Jules1, Nadège Elvire Njoh2, Ronald Komguep Nganyo2 and Etienne Tedonkeng Pamo1

1Department of Animal Production Animal Nutrition and production Research Unit, University of Dschang, Cameroon

2Department of Animal Production Ichthyology and Applied Hydrobiology Research Unit, University of Dschang, Cameroon

Corresponding Author:

Emile Miégoué, Department of Animal Production Animal Nutrition and production Research Unit, University of Dschang, Cameroon

Keywords

Clarias gariepinus ; Production Cost; Lima Bean; Fish Meal; Growth

Abstract

A study on the effect of the substitution of fishmeal by Lima bean flour was conducted between March and May 2018 within the AIO ICG of the Batié District, with the global objective of contributing to the development of alternative sources of animal protein. Specifically, the aim of the study was to evaluate the effect of the substitution of fishmeal by Lima bean flour on the growth performance, survival and feed cost of Clarias gariepinus. For this purpose, 300 fry of Clarias gariepinus with an average weight of 3 ± 1.41g were divided into five batches and fed three times a day with rations corresponding to 5% of their ichthyo biomass. The rations R0, R25 R50, R75 and R100 respectively corresponded to the substitution rates of 0, 25, 50, 75 and 100% of fish meal by that of Lima bean. The physic-chemical characteristics of the water (pH, temperature, dissolved oxygen, nitrites and nitrates) were measured daily. The following results were obtained: The highest weight gains were obtained with the rations R25 (20.56 ± 0.40 g), R50 (20.64 ± 0.32 g), R75 (20.98 ± 0.46 g) and the lowest with the ration R100 (16.21 ± 0.28 g). For this average daily gain, the highest values were 0.36 ± 0.02 g; 0.37 ± 0.01 g, 0.38 ± 0.01 g respectively for the R0, R50 and R75 rations and the lowest with R100 (0.29 ± 0.01 g). The highest value of the specific growth rate (2.47 ± 0.07%) was obtained with the ration R0 and the lowest (1.61%) with the ration R100. The consumption index reached its highest and lowest values with the rations R100 (4.74 ± 0.42) and R50 (3.57 ± 0.43) respectively, compared to the value of the ration R0 (3.31 ± 0.37) for this parameter. Concerning the condition factor K, the highest value was recorded with the R50 diet (1.11 ± 0.49) while the lowest value was obtained with the R75 diet (0.95 ± 0.45). The cost of producing one kilogram of food was higher with the R25 ration (504.59 FCFA) and lower with the R100 ration (443.20 FCFA). This study found that incorporating 75% Lima bean flour into the feed increases the growth performance of Clarias gariepinus fry and reduces the cost of food production.

Citation

Miégoué E, Zebaze PDT, Tendonkeng F, Jules L, Njoh NE, Nganyo RK, et al. Effect of Fishmeal Substitution by Lima Bean Meal on the Zoo Technical Performances of African Catfish (Clarias gariepinus) in the Batié Sub-Division, West Region of Cameroon. Int J Fisheries Sci Res. 2018; 2(2): 1009.

Introduction

Global fish production and demand are steadily increasing and have increased fivefold in less than 10 years [1]. Production increased from 39 million tons in 2010 to 174.1 million tons in 2016 [2]. In addition, its global per capita consumption per year has increased from an average of 9.9kg in the 1960s to over 20kg in 2016 [2]. In sub-Saharan Africa, fish products contribute an average of 50% of GDP in protein intake of animal origin but are still insufficient [3]. In Cameroon, the high protein demand linked to the impetus of the demographic growth of the population is generating interest in fish farming, which represents an alternative that can promote the self-sufficiency of rural populations and food security [4]. However, fish farming faces many constraints, the main ones being the lack of fry and quality feed, the unavailability of by-products and the high costs of imported food [5,6]. Because of the high costs of imported feeds and the unavailability of certain ingredients, the protein component, mainly made of fishmeal, remains the most expensive [7], and it is urgent to find alternative sources available and less expensive. Thus, several studies have been conducted on the substitution of fishmeal by other protein sources, whether of plant or animal origin [8,9]. Hence, this has led to the initiation or the attempt to replace total or partial fish meal with that of Lima bean (Phaseolus lunatus). The species Phaseolus lunatus is one of the least used legumes in Cameroon. This bean has an amino acid profile similar to that of common beans [10,11], but because of the ignorance of its nutritional potential, its culture is neglected. Thus, in order to get breeders to take an interest in this alternative source of protein, this research work has been initiated with the general objective of contributing to the development of alternative sources of protein in the diet of fish. More specifically, it was discussed to evaluate the effect of Lima bean flour on the survival rate, growth performance and finally on the economic cost of producing Clarias gariepinus.

Material and Methods

Study zone

The study took place within the Joint Initiative Group of Integrated Western Aquaculture (ICG AIO), located between 5°17’0 ‘’-5°18’53 ‘’ of latitude North and 10°17’0 ‘’ - 10°19’31 ‘’ east longitude and at an altitude of 1700 m in the West Region of Cameroon, Haut Plateaux Division, specifically in the Batié Sub-division. The climate is the Sudano-Guinean type and includes a rainy season (mid-March to mid-November) and a dry season (mid-November to mid-March). The temperature and average rainfall are respectively 23°C and 1621 mm/year.

Biological material

Three hundred (300) Clariasgariepinusfry with a mean weight of 3 ± 1.41 g and a mean total length of 7 ± 1.45 cm were used. These fry were divided into five (5) batches according to the different diets tested. The loading of these fry, resulting from an artificial reproduction made within the GIC, was 20 fry per basin. Lima bean (Phaseoluslunatus) and agricultural byproducts were purchased from the Bafoussam city market.

Production of Lima bean flour

Fourteen (14) kilograms of beans were boiled 100°c for 2 hours and then dried under the sun to constant weight. It was then crushed and mixed with other agricultural by-products according to the food rations formulated.

Experimentation and data collection

To carry out this work, fifteen (15) circular basins of 1m3 each, fed with drilling water were used. The volume of water in each basin was 900 liters and renewed to two-thirds (2/3) every day. To this, three hundred (300) Clarias gariepinus fry were randomly divided into five comparable lots of size and weight with three replicates per batch. Each batch was randomly assigned to one of the R0, R25, R50, R75 and R100 experimental diets formulated. The compositions and the bromatological characteristics are given in Table 1. The feed was distributed three times a day (7am, 12h and 18h) at 5% of ichthyobiomass [12,13] for 56 days during the experiment, and the quantity was readjusted after each control fishery.

Table 1: Food Composition and Bromatological Characteristics and Cost of Different Rations.

feeds/Ingrédients in % R0 R25 R50 R75 R100
Fish meal 18.6 13.9 9.3 4.7 0
Bean flour 0 4.7 9.3 13.9 18.6
Corton cakes 18.6 20.2 18 18 24.9
Soybean meal 18.5 20.2 22 23 24.9
Peanut cake 18.6 20.2 17 23 24.9
Removing wheat 7.8 5.4 3.2 3 0
Rice flour 7.8 5.4 3.2 4 0
CMAV 5 5 5 4 5
Palm oil 3.8 3.8 5 3 4
Cassava 1.5 1.5 1 2 1
Total 100 100 100 100 100
Bromatological characteristics
Crude protein (% DM) 39.8 40.14 40.07 39.9 39.93
Metabolizable energy 2714.86 2701.85 2752.1 2619.04 2797.2
kcal / g
Calcium g/kg 1.7 1.43 1.24 0.94 0.74
Phosphorus g / kg 1.15 1 0.86 0.7 0.58
Ca/P 1.49 1.43 1.42 1.35 1.27
Price of one kg of feed 522.19 504.59 487.09 469.48 443.2

Every two weeks, a control fishery was conducted and 25% of the fish in each treatment were individually weighed using an electronic scale of 0.1 gram precision and measured with a 0.1mm precision icthyometer. This made it possible to evaluate the growth characteristics of the fish and readjust the quantity of food to be distributed during the two following weeks.

In parallel with the data collection, the physical and chemical parameters of the water were obtained in situ between 06:00 and 07:00 in each basin: it consisted of taking the temperature, the pH, the ammonia, the nitrites, nitrates and dissolved oxygen from the water respectively using a HANNA mini-maxi thermometer, a Waterproof pH meter, a Tera nitrite chemical kit, and an EUTECH instrument or meter instrument. At the end of the test, all the fish were counted, weighed and measured.

Survival rate and growth parameters

Loss of survival (%) = (Final number of fish/Initial number of fish) x100.

Weight gain (g) = Final average weight - Initial average weight.

Average daily gain (g/d) = Weight gain/time (number of days).

Specific growth rate (%) = [ln (final average weight) - ln (initial average weight)] * 100/time; ln = natural logarithm.

Condition factor K (%) = (W/LT3) x100 with W = weight in g, L = total length.

Consumption index = quantity of food served/weight gain.

Financial evaluation

Financial evaluation of the ration was made on the basis of the prices of the different ingredients on the market and on the basis of the cost of production of the kilogram of Lima beans.

Cost of Feed Consumption = Cost of Kg of Feed x Feed Consumption.

Production Feed Cost = Feed Consumption Cost x Consumption Index.

Statistical analyzes

The growth and biochemical parameters were expressed on average plus or minus standard deviation and in percentages. One-way analysis of variance (ANOVA) was used to test the effects of treatment and the Ducan test at the 5% threshold to separate the averages when there was a significant difference. SPSS 20.0 software was used.

Results and Discussion

Results

Effect of the substitution of fishmeal by Lima bean meal in the feed on the survival rate of Clariasgariepinus.

The effect of fish meal replacement by Lima bean flour on the survival rate of Clariasgariepinus is shown in Figure 1.

Figure 1: Effect of fishmeal substitution by Lima bean meal on the survival rate of Clarias gariepinus.

R0-R100 : Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour; TS: survival rate.

It shows that the highest survival rate (98.4 ± 2.3%) was obtained with the R50 ration followed by R75 and R100 (97.6 ± 2.5%). The lowest value (96.5 ± 2.5%) was recorded with the R25 diet, although no significant difference was observed between the diets (R0, R25, R50, R75 and R100).

Effect of fishmeal substitution by Lima bean flour on the growth characteristics of Clariasgariepinus: The effect of the substitution of fishmeal by Lima bean flour on growth characteristics is summarized in Table 2 and illustrated in Figures 2 to 6.

Figure 2: Effect of the substitution of fishmeal by Lima bean meal on the weight gain of Clarias gariepinus.

R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour.

Figure 3: Effect of the substitution of fish meal by bean flour on the average daily gain of Clarias gariepinus.

R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour.

Figure 4: Effect of the substitution of fishmeal by Lima bean flour on the specific growth rate of Clarias gariepinus.

R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour.

Figure 5: Effect of the substitution of fishmeal by Lima bean meal on the overweight of Clariasgariepinus.

R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour.

Figure 6: Effect of fishmeal substitution by Lima bean meal on the consumption index of Clarias gariepinus.

R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% Lima bean flour.

Table 2: Values of zoo technical characteristics according to the substitution rate of fishmeal by Lima bean flour.

Parameters R0 R25 R50 R75 R100
Ni 60±0 60±0 60±0 60±0 60±0
Nf 57.5±1.50 58±1.00 56±1.50 58±0.50 59±0.50
GP (g) 20.25±0.44b 18.56±0.4b 20.64±0.32b 20.98±0.46b 16.21±0.28a
GMQ (g) 0.36±0.02b 0.33±0.01a 0.37±0.01b 0.38±0.01b 0.29±0.01a
TCS (%) 2.33±0.07b 2.20±0.05b 2.47±0.1b 2.51±0.45b 1.61±0.04a
K 0.99±0.38a 1.01±0.43a 1.11±0.49a 0.96±0.38b 0.95±0.45b
IC 3.31±0.37b 3.63±0.52b 3.47±0.43b 3.68±0.28b 4.74±0.42a

Ni: Initial Number of Fish; Nf: Final Number of Fish, GP: Weight Gain; GMQ: Average Daily Gain; TCS: Specific Growth Rate; IC: Consumption Index; K: condition factor; R0-R100: Rations containing respectively 0%, 25%, 50%, 75% and 100% of Lima bean flour.

(a,b,c) averages with the same letters for the same line are not significantly different (p˃0,05).

It is generally apparent that all characteristics were significantly affected. From Table 2, it appears that the R100 diet gave the significantly (p<0.05) lowest weight gains (GP). On the other hand, no significant (p>0, 05) difference (p>0, 05) was observed between the other treatments. Regarding average daily earnings (ADG), the lowest significant (p<0.05) value was obtained with the R100 ration. The latter was comparable (p>0, 05) to rations R25. The R75 diet gave the highest value but comparable (p>0, 05) to that of the R0 and R50 values.

With respect to the specific growth rate, the values were comparable (p>0, 05) with the R0 to R75 diets and significantly low with the R100 diet. With regard to the condition factor K, it recorded the values significantly (p<0.05) higher with the ration R50, R25 and R0 and significantly (p<0.05) lower with the R75 and R100. The opposite trend was observed with the consumption index. The R100 ration gave the significantly (p<0.05) higher index value.

Effect of fish meal substitution by Lima bean meal on Clarias gariepinus weight gain: The effect of fish meal replacement by Lima bean flour on the weight gain of Clarias gariepinus fry, as shown in Figure 2, shows that, in general, weight gain has increased over time regardless of the food ration experienced. However, weight gains were significantly greater with the R75 (20.98 ± 0.46g), R50 (20.64 ± 0.32g), R0 (20.25 ± 0.44g) and R25 (18.56 ± 0.40 g) in contrast to the R100 diet which was the lowest value (16.21 ± 0.28 g).

Effect of fish meal substitution with lima bean meal on average daily gain of Clarias gariepinus fry: Figure 3 illustrates the effect of fish meal replacement by Lima bean flour on average daily gain in Clarias gariepinus fry. In general, it appears that the average daily gain has increased throughout the study period regardless of the treatment.

However, it was significantly (p<0.05)higher with the R0 (0.36 ± 0.02g), R50 (0.37 ± 0.01g) and R75 (0.38 ± 0.01g) rations, while the most less values 0.33 ± 0.01 g and 0.29 ± 0.01 g were obtained with R25 and R100 respectively.

Effect of fish meal replacement by lima bean meal on the specific growth rate of Clarias gariepinus: The effect of fish meal replacement by lima bean meal on the specific growth rate of Clarias gariepinus (Figure 4) shows that R0 (2.47 ± 0.07%), R25 (2.2 ± 0.05%), R50 (2.33 ± 0.1%) and R75 (2.18 ± 0.45%) were significantly (p<0.05) higher than the R100 diet (1.61 ± 0.04%) which recorded the lowest value.

Effect of fishmeal substitution by lima bean meal on the condition factor of Clarias gariepinus: The effect of the substitution of fishmeal by Lima bean flour on the condition factor K is shown in Figure 5. It is apparent that, overall, the trend, the profile and the pace are comparable between treatments. However, the rations R50 (1.11 ± 0.49), R25 (1.01 ± 0.43) and R0 (0.99 ± 0.38) recorded the significantly (p<0.05) highest values, unlike the 0.96 values ± 0.38 and 0.95 ± 0.45 of R75 and R100 respectively (Table 3).

Table 3: Correlation between the characteristics of Clariasgariepinus and the physicochemical parameters of water.

Rations Growth correlation      
characteristics
  T(°C) pH NO2 NO3(mg/l) Oxygen
-
(mg/l)
  K 0.351 0.163 0.773 -0.026 -0.903
 
 
  IC 0.999* -0.889 0.84 -0.959 -0.686
  GMQ 0.639 -0.169 0.938 -0.353 -0.994
R0 Poids 0.371 0.143 0.785 -0.047 -0.911
  K -0.087 -0.574 0.423 0.423 -0.201
 
 
  IC -0.437 -0.828 0.071 0.071 -0.537
  GMQ 0.765 0.985 0.341 0.341 0.834
R25 Poids 0.292 -0.225 0.731 0.731 0.181
  K -0.941 0.988 -0.848 -0.779 0.628
 
 
  IC -0.637 0.771 -1.000* -0.349 0.937
  GMQ 0.357 0.174 0.513 -0.643 -0.766
R50 Poids 0.995 -0.996 0.693 0.908 -0.419
  K -0.995 -0.894 -0.893 -0.056 -0.138
 
 
  IC -0.614 -0.941 -0.289 0.685 0.622
  GMQ 0.165 0.667 -0.201 -0.949 -0.919
R75 Poids -0.941 -0.976 -0.756 0.189 0.108
R100 K 0.52 -0.024 0.854 -0.155 -0.024
  IC 0.989 -0.931 -0.15 -0.971 -0.931
  GMQ 0.866 -1.000** -0.499 -0.991 -1.000**
  Poids -0.971 0.961 0.241 0.989 0.961

*Correlation is significant at 0.05 (bilateral)

**Correlation is significant at 0.01 (bilateral).

Effect of fishmeal substitution by Lima bean meal on the consumption index of Clarias gariepinus: The consumption index of Clarias gariepinus, as illustrated in Figure 6, was significantly (p<0.05) affected by the substitution of fishmeal with Lima bean flour. Thus, the lowest index value (3.31 ± 0.37) was recorded in the lots that received the R0 ration followed by the R50 ration (3.47 ± 0.43) and the highest (4.74 ± 0.42) was obtained with the ration R100. This characteristic tends to increase with the level of substitution.

Correlation between the growth characteristics of Clariasgariepinus and the physicochemical parameters of water in general, the growth characteristics were not influenced by the physical and chemical parameters of the water, with the exception of the consumption indices of the R0 and R50 diets, which significantly (p<0.05) were affected by the temperature of the water and the rate of nitrite; and mean daily gain (ADG) that was significantly influenced (p<0.05) by pH and dissolved oxygen.

Financial evaluation

The economic evaluation of the different rations is summarized in Table 4. It appears that the ration R100 had the lowest production price (443.2 FCFA), followed by rations R75 (469.48 FCFA) and R50 (487.09FCFA). However, the best value for money was obtained with the R75 ration.

Table 4: Evaluation of the cost of different rations.

Experimental R0 R25 R50 R75 R100
rations
Price of a kg of 522.195b 504.59b 487.09b 469.48a 443.20a
feed
Feeding cost of 1044.39 787.16 774.47 1065.72 899.69
a kg of fish

Discussion

The results show that survival rates were not significantly affected by the different percentages of fish meal substitution by Lima bean f lour. This rate varied from 96.5 ± 2.50 to 98.4 ± 2.30%. These results are similar to those obtained by Pouomogne [14] who recorded a maximum survival rate of 96.66% and those of Keremah et al. [15] who recorded a survival rate ranging from 76.7 to 96.7%. The lack of difference reflects the fact that Lima beans can substitute fishmeal without affecting the survival of fish.

Results on growth characteristics indicated that the weight gain, average daily gain, and specific growth rate of fish fed with the feed containing varying levels of Lima bean meal were significantly comparable to those in the diet. Fish receiving the control diet, with the exception of fish fed with the R100 diet. This result would indicate that the proteins and other nutrients contained in lima bean were well assimilated by Clariasgariepinus fry, indeed [16], by evaluating the influence of a food-based diet of Lima bean in Oreochromisniloticus, indicated that a substitution of fishmeal by that of Lima bean increased the growth of O. niloticus fry. During this experiment, the ration containing approximately 20% fishmeal gave the best results. This result is contradictory to that of Ekoué et al. [17] who observed that a feed of similar formulation gave better results with substitution rates of 30 and 60% of fish meal by the Lima bean flour in juveniles of Clariasgariepinus. However, the values of average daily maximum gain recorded in this study (0.35g/d) are greater than those obtained by Gandaho [18] with moringa leaves (0.19g/d) but remain ten times lower than 3g/day obtained by Micha [19] and Lacroix [20] in juveniles of Clariasgariepinus fed with feed containing respectively 40 and 30% protein and raised to 30°C. This could be justified by environmental conditions different from those of these studies, particularly the average temperature which has been around 23.01°C. The same observation is true for the specific growth rate (1.61% to 2.51%), which is higher than 0.78% reported by Keremah et al. [21] but lower than 4.14%. 5.80%/d obtained by Toko [22] in Clariasgariepinus and also lower than those obtained by Kanangire [23] in the same species, which are between 4.26; 4.05 and 3.85%/day obtained respectively for feed at Azolla (0%, 30%, and 50%). These poor performances could be justified by the conditions of the test. Indeed, the average temperatures (23.01°C) of our tests were low compared to 27.4°C Keremah et al. [21]. However, the thermal interval favorable to good growth of Clarias juveniles is between 26 and 30°C (Baras and Jobling, [24]. The observed difference could also be related to the genetic material used as to the quality of the feed because the specie is an omnivorous species with a carnivorous tendency.

The condition K factor that gives the fish overweight has varied with treatments and was greater than 1 for the R25 and R50 treatments showing a good weight according to Fulton which reports that K>1 reflects a good weight of the fish. Indeed, the K factor obtained in Clarias gariepinus during the test was between 0.95 and 1.11. These values were comparable (P>0.05) to those (0.62 to 1.86) reported by Mlewa et al. [25] in Protopterus aethiopicus and higher than those reported by Rukera et al. [26]. (0.79 to 0.83%) in Clarias gariepinus reared at multiple densities and fed with complete feed or reported by Ekoué [17] (0.06 to 0.74). The difference between these values would be related to the optimal use of plant resources in breeding.

Regarding dietary parameters, the consumption index was significantly comparable between the different diets (R0, R25, R50 and R75). However, the consumption index values recorded during the study (3.31 ± 0.37 to 4.74 ± 0.42) are far superior to the values of 1.3 and 1.7 found by Lacroix. (2004) by feeding fish in floating cages using a feed that measures 30% crude protein at a density of 100 individuals/m3. Similarly, this index was also higher than that reported by Yakubu et al. [27] at a density of 95 individual/m3. In this study, in general, the incorporation of Lima bean flour increased ingestion in Clarias gariepinus fry relative to the control diet (R0). This observation makes it possible to assume that the foods tested were more appreciated by the Clarias gariepinus fry than the R0 control food; however, their assimilation has been variable.

The food R75 represents the best value for money (469.48 FCFA per kg of food purchased and 1065 FCFA obtained per kg of fish sold) and is therefore the most efficient bioeconomically.

Conclusion

At the end of the study on the effect of the substitution of fishmeal by Lima bean flour, aimed at contributing to the development of alternative sources of animal protein the following conclusions were drawn:

The survival rate of Clarias gariepinus fry was not significantly affected by the substitution rate.

However, the highest survival rate was recorded with the lot fed with the R50 ration; all growth characteristics were significantly affected by the substitution rate.

However, it should be noted that the best characteristics were obtained with the ration R50; the feed containing 75% Lima bean flour is the most bioeconomically efficient.

In view of the above, the use of the ration substituted for 75% Lima bean increases the growth performance of Clarias gariepinus fry and reduces the cost of food production. However, the influence of Lima bean flour on reproductive parameters and the technological and organoleptic qualities of fish flesh should be examined.

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22. Imoroutoko Halieutique Poissons Bénin) I. (Whedos) Par Poissons-Chatsclarias La Amélioration Des Trous Du Promotion Gariepinuset De Delta De La Traditionnels De Production À l’Ouémé L’élevage Heterobranchuslongifilis. (Sud Des Thèse Présentée En Vue De L’obtention Du Grade De Docteur En Sciences, Facultés Universitaires Notre-Dame De La Paix Namur-Belgique, Faculté Des Sciences. 2007 ; 214.

23. Kanangire CK. Effet De L’alimentation Des Poissons Avec Azolla Sur L’écosystème Agropiscicole Au Rwanda. Dissertation Présentée En Vue De L’obtention Du Grade De Docteur En Sciences. Facultés Universitaires Notre -Dame De La Paix, Namur, Belgique. 2001; 220.

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Other Articles

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Massive Chinese Fleet Jeopardizes Threatened Shark Species around the Galápagos Marine Reserve and Waters off Ecuador: Implications for National and International Fisheries Policy

Being a UNESCO-World Heritage Site, the Galápagos harbors the largest global shark biomass in the world’s oceans and a unique marine biodiversity.

Alava JJ1,2*, Barragán-Paladines MJ3, Denkinger J4, Muñoz-Abril L4, Jiménez PJ2, Paladines F5, Valle CA4, Tirapé A6, Gaibor N7, Calle M6, Calle P6, Reyes H8, Espinoza E8 and Grove JS9


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The Relationship between Behavior Responses and Brain Acetylcholinesterase (AChE) Activity of Zebrafish (Danio rerio) in Cadmium Stress

In this research, the toxic effects of Cadmium chloride (CdCl2 ), which can seriously pollute aquatic environment and threaten human health, are evaluated based on the behavior responses and the brain Acetylcholinesterase (AChE) activity of zebrafish (Danio rerio). The results showed that Behavior Strength (BS) of test groups (changed from 0.15 to 0.65), which was recorded using an online behavior monitoring system, was lower than the control groups (changed from 0.65 to 0.85). The behavior responses of zebrafish suggested that both dose and time effect relationships existed between Cd2+ stress and zebrafish BS. Meanwhile, the brain Acetylcholinesterase (AChE) activity of zebrafish were strongly inhibited by Cd2+: the AChE activities were lower than 60% after 0.5h Cd2+ exposure in both 1 TU (Toxic Unit) and 2 TU. The AChE activities in 0.1 TU Cd2+ treatment were about 60% in the first 2h and then increased to about 100% in 4h with a decrease tendency in the following exposure time (8h to 48h), which changed from 100% to 70%-80%. Totally, the brain AChE activities of zebrafish showed similar rules with BS after correlation analysis, which might provide an understanding of the ecotoxicological assessment of heavy metal Cd based on zebrafish.

Meiyi Yang1,2#, Lizhen Ji1,2#, Xu Zhang2, Yuqi Fan1,2* and Zongming Ren1,2*


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Neritic Larval Fish Distribution in the Oceanic Area of the Campeche Bay, Gulf of Mexico

Composition and abundance of larval fishes in Campeche Bay were studied during two seasons, winter, 2013 (24 stations) and summer, 2014 (31 stations). Sampling was carried out with open-close nets, mouth 75 cm and 505 µm mesh. The data of salinity and temperature allowed distinguishing three oceanic sub-regions: North, East, and West. There were 236 taxa, belonging to 74 families, 168 species, 154 taxa occurred in winter and 171 in summer; the composition in both cruises was similar with around 70 % of oceanic and 30 % of neritic larvae. The larval density was almost three times larger in summer than winter. The Campeche Bay hydrodynamics fits well with the results; the West sub-region is located where a cyclonic gyre takes place, the North and East sub regions are located in the area of influence of warm currents over the Yucatan shelf. The hydrodynamics also allows understanding the differences in the proportion of neritic larvae among the three oceanic sub-regions, the West and East with the lower and higher number of neritic larvae, respectively. The large difference among regions is related to some neritic taxa occurring exclusively in some of them. Of the total taxa, 55 neritic occurred only once and it means that more than a half of neritic taxa were represented by one organism, 31 from 85 neritic taxa occurred in the layers of 600 to 1000 m depth. Of the neritic larvae, only Syacium papillosum and Apogon sp. appear among the 20 more abundant.

Flores-Coto C*, Zavala-García F and Sanvicente-Añorve L


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Effect of Photoperiod on Eggs Hatchability, Growth and Survivability of Hybrid Catfish (Heterobranchus bidorsalis X Clarias gariepinus) Larvae

This study was conducted to determine the effects of photoperiod on egg hatchability, growth and survivability of hybrid catfish (Heterobranchus bidorsalis X Clarias gariepinus) larvae, using hormone-induced spawning method. Eggs were stripped from two sexually matured and healthy female Clarias gariepinus of average weight of 1kg/each and fertilized with milt from two sexually matured male Heterobranchus bidorsalis of average weight of 2kg/each. An average of five hundred (500) eggs were introduced into each ten aquaria tanks of size 70cm x 45cm x 40cm/tank, using a pre- determined spoonful estimation at five photoperiod regimes: (T1) 24L:00D (Light:Darkness); (T2) 18L:6D; (T3) 12L:12D; (T4) 6L:18D and (T5) 00L:24D in two replicates. Aquaria tanks were arranged in a flow- through system at a flow rate of 1.5L/min with aerators to maintain good water condition. Provision of light during the night for illumination of the aquaria tanks was kept constant at 1200 1x, using solar panel (Mono)/inverter (Microtex) light energy. Growth and survivability of the fish larvae were monitored for six weeks. They were fed with laboratory-cultured live feed (Daphnia) to achieve maximum feed utilization. Percentage hatchability of eggs and best growth performance of fish larvae were significantly (p<0.05) highest (92.5%, 91.2 ± 0.21mg) respectively in T5 (00L:24D), while percentage survivability of hatchlings was significantly (p<0.05) highest (94.4%) in T3 (12L:12D). It was observed in this study that the highest hatchability of eggs and optimum growth performance of hatchlings were under complete darkness, with reduced survivability of fish, as a result of observed cannibalism. The fish were photophobic. To achieve a balance result in terms of hatchability of eggs, growth and survivability of fish fry, it is suggested that incubation and hatching of eggs should be done under complete darkness, while rearing of fry should be under equal light and darkness exposure.

Adebayo IA*


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Empirical Assessment of Fish Diversity of Uttar Pradesh, India: Current Status, Implications and Strategies for Management

About 60-70% of world’s biological resourcesis contributed by India, of which fish represents 80% of the global fishes. Uttar Pradesh blessed with vivid aquatic bioresources in innumerable forms contributes about 14.68% of Indian fish biodiversity with substantial scope of inland fisheries development and aquaculture. Ganga, the mighty river of this state reportsabout 265 freshwater species from its river system [1]. Besides, other rivers viz. Ramganga, Gomti, Ghaghara, Yamuna, Gandak, Kosi and Damodaract as reservoir of different f ish stocks. In past, no study highlights the assessment of the fish biodiversity of this state in holistic way except by Khan (2000) who justreported a compilation of 129 fishes under 27 families [2]. To substantiate and revise the assessment, the fish diversity of this state was assessed by investigating these rivers, analyzing and documenting the information on different fisheries measurements including biology, distribution and conservation status. About 10,000 individuals were collected and the analysis of individuals revealed 126 fish species under 28 families and 74 genera nearly mitigating the earlier reports. The highest species diversity was recorded in the river Ganga (90) followed by Gerua (87) and then Gomati (68). 37 species were found common in Gomati, Ghaghara, Ganges, Son, Tons and Yamuna. Out of 90 species, 6 species were recorded from the river Ganga. In addition, the new distribution of a threatened torrent catfish Amblyceps mango is was recorded from the rivers Gomati, Ganga and Ramganga. The economical assessment unravels nearly 33% as ornamental, 87% as food and 10% as sport fishes.

Pathak AK*


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Stranding of Small Cetaceans with Missing Fins Raises Concerns on Cetacean Conservation in Ecuador: Bycatch or Targeted Fisheries?

Among anthropogenic threats to marine mammals, bycatch is one of the major and increasing concerns. This report describes three species of small cetaceans, including a short-beaked common dolphin (Delphinus delphis), a bottlenose dolphin (Tursiops truncatus), and two dwarf sperm whales (Kogia sima), which were found stranded with pectoral fins, dorsal fins and caudal fin removed. The dolphins were found at the beaches of San José de Las Nuñez and San Pablo, respectively (Santa Elena Peninsula Province on 14 August 2017), while the dwarf sperm whales were found in Puerto Lopéz and Crucita (Manabí Province) in July 2014 and August 2015, respectively. Possible explanation for the dolphins and dwarf sperm whales missing fins support the event as a possible case of fishery interaction or bycatch with systematic removal of their fins. Although remnants of artisanal gillnets were not found near the two dolphin species, one of the dwarf sperm whales showed marks of artisanal gillnets on the body as evidence of bycatch. Trade of dolphin carcasses and their parts for bait by fishers cannot be ruled out as there is some evidence of this practice in the past. Both dolphins species are vulnerable species at the national level and commonly involved in incidental captures with gillnets of artisanal fisheries in Coastal Ecuador. Cetacean bycatch is a grave conservation problem affecting several cetacean species in Ecuador’s waters. Fisheries and environmental authorities must be vigilant and enforce actions to proactively mitigate possible anthropogenic impacts and promote environmental education activities in fishing communities to conserve vulnerable dolphin species in Ecuador’s waters. Further, to comply with new rules and regulations of the US Marine Mammal Protection Act (MMPA) intended to reduce the bycatch of marine mammals in foreign commercial fishing operations that export fish and fish products to the United States, a regulatory program is urgently needed to mitigate and reduce fisheries interactions with marine mammals in Ecuador.

Pedro J Jiménez1, Juan José Alava1,2*, Cristina Castro3, Jorge Samaniego4 and Patricia Fair5


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Sodium Arsenite-induced Morphological, Behavioral, Hematological and Histopathological abnormalities in Labeo Rohita

Toxic metals have contaminated the aquatic ecosystems to a large scale, and they eventually enter human systems by contaminated air, food, water and soil. Recently, arsenic toxicity has become an alarming concern around the globe. Major areas of North-Eastern states of India have been demarcated with an arsenic content of 50-1000 µg/l in drinking water sources and aquatic ecosystems. Arsenic range in Barak Valley is many folds higher than the permissible limit of WHO and BIS as 10µg/l and 50µg/l respectively, which is present in the form of Sodium Arsenite in water. Fishes are the major dwellers of aquatic ecosystem and serves as good bio-indicators for determination of health status of an aquatic ecosystem. They also form the staple diet of North Eastern people. Labeo rohita is one of the most commonly available and consumed in large scale. The present study was carried out in Labeo rohita in vivo. Labeo rohita (n=10) of similar size and weight were exposed to sodium aresnite at concentrations 100 µg/l and 250 µg/l along with controlled set up for 10 days. The morphological, behavioral, hematological and histopathological changes were evaluated. Fishes exposed to Sodium arsenite showed irregular ocular movement, fin movement, swimming pattern and loss in scales with higher prominence in 250 µg/l of arsenic group than those at 100 µg/l. The hematological indices revealed decrease in RBC count and increase in WBC count in both sodium arsenite exposed groups. The histopathological study of liver revealed parenchymal disorganization and atypical residual body in both sodium arsenite treated groups. Results obtained showed major damages to fishes due to contamination with sodium arsenite. These fishes, when consumed by humans, leads to increase in several thousand folds of sodium arsenite by means of biomagnification. High exposure of arsenic in human through fishes leads to several disorders. The possible way of eradicating sodium arsenite entry into humans is banning fishing activities in highly contaminated aquatic ecosystems. Community education and local participation are also essential to get a fruitful outcome.

Rajib Biswas1* and Soumitra Nath2


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Reconstruction of Historical Fisheries Profile of Cameroon

This work attempts to reconstruct historical fisheries profile by filling in the missed underestimated catch information for some reasons of industrial fishing, artisanal fishing, inland fishing, illegal fishing, discards and aquaculture production of Cameroon from 1950 to 2016.This reconstruction was carried out based on data published by various authors, the Ministry of Fisheries and Livestock (MINEPIA), the Limbe Research Center on Fisheries and Oceans and FAO reports. The dataset allowed us to reconstruct the fishing profile of Cameroon by completing the missing data by interpolation. Then we compare the data obtained with those of FAO. Reconstructed catches were estimated at 13,834 tons and aquaculture production was estimated at 19 tons in 1950 compared to 12,000 tons and 14 tons published by FAO, With the agricultural reforms and development of projects focused on the primary industry, catches increased around 94,122 tons in 1977(compared to 70,167 tons reported by the FAO) to 102,975 tons in 1981(compared to 79,761 tons reported by the FAO), declined to 78,790 tons in 1986 because of the reduction of the Exclusive Economic Zone of Cameroon (EEZ) by the geographical presence of the insular part of Equatorial Guinea (Malabo Island), then increased to 186,204 tons in 2005(compared to 142,345 tons reported by the FAO), declined to 154,800 tons in 2008(compared to 129,000 tons reported by the FAO). Since 2011 it became stable and reached around 240,000 tons against 220,000 tons published by FAO. Overall, there are discrepancies between the reconstructed data and the data provided to FAO: the reconstructed data is 30% higher than the FAO data. This information about fisheries production in Cameroonian waters shows that many locals, fisheries managers and stakeholders depends on fish products for either incomes or food safety; therefore, the recent decline of fish production in Cameroon is of no good sign to the abovementioned persons. These observed fish production decline indirectly threatens the food security of the people of Cameroon and low financial income to the state coffers.

Nyatchouba Nsangue Bruno Thierry, Richard Kindong and Liuxiong Xu*


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Comparative Effect of Monoculture and Polyculture in Two Species of Clariidae: Heterobranchus longifilis and Clarias gariepinus in Post Fingerlings Growth

In order to improve the production of Clariidae, a study on the type of cultivation of Heterobranchus longifilis and Clarias gariepinus in post fingerlings growth phase was carried out in tanks. It took place from March to May 2018 at the IRAD fish station in Koupa-Matapi (LN: 5º 21 ‘to 5º 58’ and LE: 10º 17 ‘to 11º 02’) west region Cameroon. For this fact 180 fry therefore 90 Heterobranchus longifilis and 90 Clarias gariepinus with an average weight 3.55 ± 0.68 g; 8.46 ± 0.41cm of total length and 7.37 ± 0.30 cm of standard length were used. The 180 fry were divided into three treatments of 60 individuals (T1 treatment: Clarias gariepinus, T2 treatment Heterobranchus longifilis and T3 treatment: Clarias gariepinus + Heterobranchus longifilis). Each treatment was repeated twice. The fish were fed twice per day at a rate of 10% of the ichthyobiomass readjusted each month after control fishing with a feed at 42% crude protein. From the results of this trial, it appears that unlike the higher mortality rates (11.66 ± 2.36%) recorded in monoculture Clarias gariepinus, the highest cannibalism rates were obtained in monoculture of Heterobranchus longifilis (13.33 ± 4.71%). The survival rate was not influenced by the type of culture. Nevertheless, the highest rate (94.44 ± 0.00%) was observed in Heterobranchus longifilis in polyculture. The highest growth values were recorded for C. gariepinus in polyculture and the weakest for H. longifilis in polyculture. For linear growth, the highest values were recorded in C. gariepinus in monoculture. In order to reduce the rate of cannibalism and mortalities in Clarias gariepinus and Heterobranchus longifilis in post f ingerlings growth phase, it is preferable to combine these two species.

Nana Towa Algrient¹, Nanmegni Rostand Romeo¹, Tonfackachille Peguy², Efole Ewoukem Thomas¹ and Jouokou Salifou²


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Delayed Fertilization of Landlocked Fall Chinook Salmon Eggs Stored with Oxygen at Two Temperatures

This study examined the use of supplemental oxygen and two temperatures (1° and 11°C) during the four hour storage of unfertilized landlocked fall Chinook salmon (Oncorhynchus tshawytscha) eggs from Lake Oahe, South Dakota, USA. There was a significant and positive effect of oxygen use on egg survival to the eyed-stage and hatch. In addition, survival to egg eye-up and hatch was significantly affected by storage temperature, with decreased survival at 1°C. However, there was no significant interaction observed between the use of oxygen and storage temperature. Mean survival to hatch ranged from 50% for those eggs stored with oxygen at 11°C compared 17.8% for those eggs stored on ice at 1°C in air. To maintain landlocked Chinook salmon egg fertility, storage with supplemental oxygen at 11°C is recommended.

Hunter Eide and Michael E Barnes*