Submit or Track your Manuscript LOG-IN

Evaluation of Growth Performance and Bioaccumulation Pattern of Metals in Catfish Species, Channa marulius and Wallago attu under Cadmium and Chromium Toxicity

PUJZ_36_2_125-130

Evaluation of Growth Performance and Bioaccumulation Pattern of Metals in Catfish Species, Channa marulius and Wallago attu under Cadmium and Chromium Toxicity

Moazama Batool1*, Sajid Abdullah2, Huma Naz3, Mubashar Hussain4, Sadia Maalik1, Sajida Mushtaq1, Tanveer Ahmed5, Laiba Shafique6

1Department of Zoology, GC Women University Sialkot, Pakistan.

2Department of Zoology, Wildlife and Fisheries, University of Agriculture Faisalabad, Pakistan.

3Department of Zoology, Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan.

4Department of Zoology, University of Gujrat, Pakistan.

5Department of Life Sciences, Khwaja Fareed University of Engineering and Information Technology, Rahim Yar Khan, Pakistan.

6State key Laboratory for Conservation and Utilization of Sub-tropical Agro-Bioresources, Guangxi University Nanning China.

Abstract | The aim of present study was to assess the growth performance and bio-accumulation of metals in Channa marulius and Wallago attu exposed to 1/3rd of LC50 of chromium (Cr) and cadmium (Cd) for 8-week. In both treatments statistically significantly, variable responses viz. wet weight gain (WG), feed intake (FI), feed conversion ratio (FCR) and specific growth rate (SGR) were determined. The control fish (unstressed) had significantly higher WG followed by Cr and Cd test mediums. The FI by C. marulius was significantly higher as 12.83±0.07 g in Cr followed by Cd (12.14±0.05 g) and control (9.57±0.364) medium. However, FI by W. attu was higher in control (15.30±0.40) followed by Cr (13.08±0.06) and Cd (11.98±0.03) exposed mediums. The cumulative FI by W. attu was greater than C .marulius in all treatments. In control, FCR of both species was better significantly than fish reared in Cr and Cd exposed test mediums. In control, SGR of C. marulius and W. attu was noted as 20.50±0.52 and 21.78±0.44, respectively that was significantly better than Cr (13.62±0.09 and 14.02±0.04) and Cd (13.55±0.05 and 13.82±0.04). The comparison between species showed that C. marulius amassed higher concentration of both metals as compared to W. attu. However, Cr accumulates at higher concentration in all organs of both fish species as compared to Cd. The amassment order for metals in both species was studied as kidney>liver>gills>skin>fins>bones>muscle.

Novelty Statement | In Pakistan, riverine system has been contaminated with varied types of toxicants such as metals which exerts negative impact on native fish species such as Channa marulius and Wallago attu. Therefore, this research provide information regarding toxic impact of metals to fish.


Article History

Received: November 20, 2019

Revised: May 03, 2021

Accepted: May 19, 2021

Published: August 21, 2021

Authors’ Contributions

MB excuted the research. SA planned the research work. HN and LS wrote the manuscript. MH helped in statistical analysis. S Maalik and S Mushtaq helped in lab work. TA revised the manuscript.

Keywords

Carnivorous fish, Bio-accumulation, Growth, Metals, Chronic exposure

Corresponding Author: Moazama Batool

[email protected]

To cite this article: Batool, M., Abdullah, S., Naz, H., Hussain, M., Maalik, S., Mushtaq, S., Ahmed, T. and Shafique, L., 2021. Evaluation of growth performance and bioaccumulation pattern of metals in catfish species, Channa marulius and Wallago attu under cadmium and chromium toxicity. Punjab Univ. J. Zool., 36(2): 125-130. https://dx.doi.org/10.17582/journal.pujz/2021.36.2.125.130



Introduction

All over the world, natural water bodies have been heavily polluted with heavy metals which release from industries, domestic and human activities (Azmat et al., 2012; Yaqub, 2012).

Among metals, chromium is very important because it is vital micronutrient (Piotrowska et al., 2008) and living organisms also used it as dietary supplement (Opperman et al., 2008; Stout et al., 2009). However, it is toxic when present in excess amount (Lushchak, 2008).

Cadmium is one of the dispensable metal, and extensively used in cement, paints, dyes and fertilizers (Jarrup, 2003). Cadmium has ability to amass in the environment due to its persistent nature (Javed, 2005). The presence of these toxicants may change the water quality parameters (Andhale and Zambare, 2012). In natural aquatic bodies, mostly organisms are exposed to low concentration of metals for long term duration. Now, scientists performed chronic tests in laboratory to check the sub-lethal metal toxicity to fish (Vosyliene et al., 2003) and also evaluate physiological alterations and ultimate their effects on growth of fish.

Toxicity of metal to fish mainly depends upon the water quality such as salinity, dissolve oxygen and temperature, and other toxicants (Witeska and Jezierska, 2003). Fish is a suitable bio-indicator to assess the water quality and their physiological parameters can be served as bio-marker of water contamination (Javed, 2012). Aquatic organisms uptake these heavy metals via different ways i.e., gills, body surface and intake of contaminated feed. However, which route is more important would depend upon the prevailing environmental conditions (Depledge et al., 1994).

Species-specific response to toxicants is a matter of great interest, because it is a critical factor for assessing toxicity as well. Several authors conducted research on species-specific response to a number of toxicants (Pyle and Wood, 2008).

In Pakistan, riverine system has been contaminated with varied types of toxicants which exerts negative impact on native fish such as Channa marulius and Wallago attu (Rauf et al., 2009). Therefore, in order to save these local fish in natural aquatic habitats, this study was conducted to determine their growth potentials and amassment of heavy metals (chromium and cadmium) under chronic exposure to predict possible impacts of persistent metal’s pollution on fish.

Materials and Methods

Two species, C. marulius and W. attu were obtained from natural breeding grounds and brought to laboratory at Fisheries research Farm, University of agriculture Faisalabad, Pakistan. Fish were placed in the cement tanks for acclimation (2 weeks) prior to start the growth trails. Fish were shifted to aquarium as the acclimation period completed. Both fish species (n=10) were grown, separately, under 1/3rd of LC50 concentration of chromium (Cr) and cadmium (Cd) and controlled (without metals) condition for 8 weeks with three replicates. Stocks solutions were prepared by using pure compounds (Aldrich, USA) of chromium nitrate [Cr(NO3)3.9H2O]) and cadmium chloride (CdCl2. H2O) and further dilution were made in deionized water. Both species, were fed with crumbled feed, to satiation, twice a day at 9:00 A.M and 17:00 P.M. The average water hardness of the test aquariums were maintained at 150±1.00 mg L-1, pH at7.5±0.05 and temperature at 28±0.05˚C.

 

Table 1: Metals concentration used for this study (Batool et al., 2014).

Fish species

Metal concentration (mgL-1)

Chromium

Cadmium

Channa Marulius

26.60

25.00

Wallago attu

21.67

10.00

 

Growth parameters

In both species of fish, statistically significantly variable responses viz. increase/decrease in wet weight gain (WG), feed intake (FI), feed conversion ratio (FCR) and specific growth rate (SGR) were determined on weekly basis.

Amassment of heavy metals

The procedure of Standard Methods for the Examination of Water and Wastewater (1989) was applied to estimate the concentrations of Cr and Cd in bone, gills, fins, kidney, muscle, liver and skin of both species by using Atomic Absorption Spectrophotometer (Perkin Elmer-Analyst 400).

Statistical analysis

Data were expressed as means ± SD for each parameter. ANOVA was applied on data to determine the statistical differences among various parameters under study (Steel et al., 1996). Pearson correlation coefficients were computed to find the relationships among various physico-chemical and growth parameters of both species.

Results and Discussion

Growth parameters

Results shows that exposure of Cr and Cd significantly lower the wet WG of C. marulius and W. attu as 8.29 ± 0.07 and 8.21 ± 0.04 g, respectively in relation to control (12.68 ± 0.18 g). Species-specific response shows that W. attu sowed significantly higher mean WG (9.92±2.22g) than C. marulius (9.53±1.96g). Similarly, FI was also lower for both species reared in metals exposed medium as compared to control. Comparison between species showed that W. attu had better FI than C. marulius in control and test mediums. Both species showed high FCR ration in control followed by that of Cd and Cr. Table 2 shows the data relate to growth rate of both species. During Cr exposure, the relationship of WG for both species was significantly positive with FI while same was negative with FCR. But results were different in Cd exposed medium, WG of C. marulius had inverse relation with FI and FCR while significantly direct relation with condition factor. However, WG of W. attu had significantly positive correlation with FI and same was inverse with FCR (Table 3). Previously, a wealth of studies have indicated that heavy metals affect the growth rate of various fish (Subathra and Karuppasamy, 2007). Heavy metals (Zn, Cu and Cd) significantly affect the FI and FCR of Perca flavescens which ultimately effect the growth (Sherwood et al., 2000).

Abdel-Hakim et al. (2016) reported the significant reduction in SGR, WG, FCR and survival rate of Nile tilapia (Oreochromis niloticus) under sub-lethal exposure of Cu, Hg, Pb and Cd. Ayegbusi et al. (2018) noted the decreased SGR of Clarias gariepinus with increase in PbCl2 sub-lethal concentrations for three weeks. Ko et al. (2019) observed the decrease in daily weight gain, condition factor and daily length gain of Platichthys stellatus when exposed to four different concentrations of waterborne Cr for 4 weeks. The decline in growth and length of Cyprinus carpio due to Cr exposure was reported by Shaheen and Jabeen (2015). Rahman et al. (2018) studied the reduced growth of Oreochromis niloticus under Cd stress. According to Javed (2012) metals exposure at sub-lethal level adversely affect the health and growth of fish. Bioenergetics processes of fishlike feeding, metabolism, nutrient absorption and excretion of waste material are all the important factors for evaluating the chronic effects of heavy metals (Bhavan and Geraldine, 2000).

 

Table 2: Effect of Cd and Cr on Growth performance of fish.

Growth parameters

Fish species

Treatments

Overall means

Cr

Cd

Control

WG (g)

C. marulius

8.17±0.098b

8.13±0.04b

12.30±0.040a

9.53±1.96B

W. attu

8.41±0.058b

8.29±0.046b

13.07±0.098a

9.92±2.22A

Overall Means

8.29 ±0.12B

8.21±0.08B

12.68±0.38A

CF (K)

C. marulius

1.84±0.046b

1.68±0.023c

2.38±0.012a

1.97±0.30B

W. attu

2.28±0.035b

1.52±0.025c

3.47±0.017a

2.42±0.80A

Overall Means

2.06±0.22B

1.60±0.08C

2.92±0.54A

FI (g)

C. marulius

12.83±0.067a

12.14±0.046a

9.57±0.364b

11.51±1.40B

W. attu

13.08±0.064b

11.98±0.029c

15.30±0.404a

13.45±1.38A

Overall Means

12.95±0.12A

12.06±0.08C

12.43±2.86B

FCR

C. marulius

1.57±0.075a

1.49±0.032a

0.78±0.029b

1.28±0.35A

W. attu

1.55±0.035a

1.44±0.023a

1.25±0.023b

1.41±0.12B

Overall Means

1.56±0.01A

1.46±0.02A

1.01±0.23B

SGR

C. marulius

13.62±0.098b

13.55±0.052b

20.50±0.520a

15.89±3.26A

W. attu

14.02±0.040b

13.82±0.040b

21.78±0.441a

16.54±3.71A

Overall means

13.82±0.20B

13.68±0.13B

21.14±0.64A

 

The means sharing similar letters in a row and column for each treatment and fish species in a single row are statistically non-significant (p>0.05).

 

Table 3: Impacts of different parameters on fish growth under metals stress condition.

Metal

Fish species

Step-wise regression

r/Mr

R2

Cr

C. marulius

Increase in weight (g)=2.858+0.804(Feed intake)-0.614(FCR)-1.195; S.E. = 0.054 * 0.01**

1.000

0.999

W. attu

Increase in weight (g) =0.410+0.859(Feed intake)-0.467(FCR); S.E. = 0.269 0.040**

0.983

0.966

Cd

C. marulius

Increase in weight (g)=-0.443-2.345(Feed intake)-0.727(FCR)+3.793(K); S.E.= -0.886 0.076**

0.994

0.988

W. attu

Increase in weight (g) =1.073+0.717(Feed intake)-0.767(FCR); S.E. = 0.022** 0.018**

0.999

0.998

 

FCR= Feed conversion ratio; * = Significant at p<0.05; ** =Significant at p<0.01; NS=Non-significant; R2= coefficient of determination.

 

 

 

Amassment of heavy metals

Comparison between species showed that C. marulius amassed higher concentration of both metals as compared to W. attu. However, Cr accumulates at higher concentration in all organs of both fish species as compared to Cd. The amassment order for metals in both species was studied as Kidney>liver>gills>skin>fins>bones>muscle (Figure 1 and 2, Table 3). According to Muhammad et al. (2009) the amassment of metal was greater in liver, gills and kidney than other tissues. Amassment of metals in liver may be due to its role in metabolism/detoxification of toxicants (Zhao et al., 2012). Kidney plays an important role in excretion of toxicants, while gills are the direct route of ion exchange and have large surface area that eases the fast diffusion of metals from water (Qadir and Malik, 2011).

Heavy metals accumulation in aquatic animals mainly depends on the metals concentration in water body and ability of animal to digest the metals as well as feeding habits of animal. Fish have been identified as a good bio-accumulator of inorganic and organic toxicant because it stays over a long period in water (King and Jonathan, 2003). Mahboob et al. (2016) noted the heavy metals accumulation pattern in muscles, gills, kidney and liver of Wallago attu as Pb<Cr<Cu<Fe sampled from the Indus river, Mianwali District, Pakistan. Jia et al. (2017) observed the highest concentration of toxic metals (Cd, As and Pb) in gills, liver and muscle of carnivores fish Pelteobagrus fulvidraco as compared to omnivores fish Squaliobarbus curriculus and Carassius auratus when both were exposed to Zn, Pb, Mn, Cu, Cd and Fe. Data showed the order of Cd accumulation in various organs was: liver > kidney > gonad > gills > muscles in all treatments. Freshwater fish species have a diverse affinity toward cadmium (Cd). The accumulation of of Cd primarily depends on the pathway of exposure either it is waterborne and dietary as well as route of uptake, time, concentration, environmental and internal conditions, along with size and age of exposed fish. Most of the fish species showed higher level of Cd in liver followed by gills and kidney while muscles always had comparatively lower level (Perera et al., 2015). Tilapia showed the highest accumulation of Cd in gills followed by liver and muscles (Aldoghachi et al., 2016).

Conclusions and Recommendations

This study concluded that burden of metals in fresh water system negatively effects the feeding behaviour and growth of fish. Furthermore, these metals can also accumulate in organs of fish. Therefore, concerned authorities must impose strict mitigation measures to control these hazardous metals.

Conflict of interest

The authors have declared no conflict of interest.

References

Abdel-Hakim, N.F., Helal, A.F., Salem, M.F., Zaghloul, A.M. and Hanbal, M.M., 2016. Effect of some heavy metals on physiological and chemical parameters in Nile tilapia (Oreochromis niloticus L.). J. Egypt. Acad. Soc. Environ. Dev. D. Environ. Stud.17: 81-95. https://doi.org/10.21608/jades.2016.63382

Aldoghachi, M.A.J., Rahman, M.M., Yusoff, I. and Sofian-Azirun, M., 2016. Acute toxicity and bioaccumulation of heavy metals in red tilapia fish. J. Anim. Plant Sci., 26: 507-513.

Andhale, A.V. and Zambare, S.P., 2012. Effect of nickel induced respiratory alterations in freshwater bivalve, Lamallidens marginalis. Int. Multidiscip. Res. J., 2: 01-03.

Ayegbusi, O.E., Aladesanmi, O.T., Kosemani, O.E. and Adewusi, O.A., 2018. Effects of lead chloride on growth performance of Clarias gariepinus (Burchell, 1822). Int. J. Bioassays, 7: 5638-5644.

Azmat, H., Javed, M. and Jabeen, G., 2012. Acute toxicity of aluminium to the fish (Catla catla, Labeo rohita and Cirrhina mrigala). Pak. Vet. J., 31: 85-87.

Batool, M., Abdullah, S. and Abbas, K., 2014. Antioxidant enzymes activity during acute toxicity of chromium and cadmium to Channa marulius and Wallago attu. Pak. J. Agric. Sci., 51: 1017-1023.

Bhavan, S.P. and Geraldine, P., 2000. Aberrations in various parameters of bioenergetics in the prawn (Machrobrachium rosenbergii) following exposure to endosulfan. Aquaculture, 1: 141-152.

Depledge, M.H., Weeks, J.M. and Bjerregard, P., 1994. Heavy Metals. In: Calow, P. (ed.), Handbook of Ecotoxicology. Blackwell, London.

Jarrup, L., 2003. Hazards of heavy metal contamination. Br. Med. Bull., 68: 167-182. https://doi.org/10.1093/bmb/ldg032

Javed, M., 2005. Heavy contamination of freshwater fish and bed sediments in the River Ravi stretch and related tributaries. Pak. J. Biol. Sci., 8: 1337-1341. https://doi.org/10.3923/pjbs.2005.1337.1341

Javed, M., 2012. Growth responses of fish under chronic exposures of water-borne and dietary metals. Int. J. Agric. Biol., 14: 281-285.

Jia, Y., Wang, L., Qu, Z., Wang, C. And Yang, Z., 2017. Effects on heavy metal accumulation in freshwater fishes: species, tissues, and sizes. Environ. Sci. Pollut. Res., 24: 9379–9386. https://doi.org/10.1007/s11356-017-8606-4

King, R.P. And Jonathan, G.E., 2003. Aquatic environmental perturbations and monitoring, African experience, USA.

Ko, H.D., Park, H.J. and Kang, J.C., 2019. Change of growth performance, hematological parameters, and plasma component by hexavalent chromium exposure in starry flounder, Platichthys stellatus. Fish. Aquatic. Sci., 22: 9.https://doi.org/10.1186/s41240-019-0124-5.

Lushchak, O.V., Kubrak, O.I., Nykorak, M.Z., Storey, K.B. and Lushchak, V.I., 2008. The effect of potassium dichromate on free radical processes in goldfish: Possible protective role of glutathione. Aquat. Toxicol., 87: 108-114. https://doi.org/10.1016/j.aquatox.2008.01.007

Mahboob, S., Kausar, S., Jabeen, F., Sultana, S., Sultana, T., Al-Ghanim, K.A., Hussain, B., Al-Misned, F. and Ahmed, Z., 2016. Effect of heavy metals on liver, kidney, gills and muscles of Cyprinus carpio and Wallago attu inhabited in the Indus. Braz. Arch. Biol. Technol., 59: 1-10. https://doi.org/10.1590/1678-4324-2016150275

Muhammad, A.Y., Khan, A.R. and Shakoori, A.R., 2009. Trace Metal accumulation in the liver of an endangered South Asian fresh water fish dwelling in sub-lethal pollution. Pak. J. Zool., 41: 35-41.

Opperman, D.J., Piater, L.A. and Heerden, E.V., 2008. A novel chromate reductase from Thermus scotoductus SA-01 related to old yellow enzyme. J. Bacteriol., 190: 3076-3082. https://doi.org/10.1128/JB.01766-07

Perera, P.A.C.T., Kodithuwakku, S.P., Sundarabarathy, T.V. and Edirisinghe, U., 2015. Bioaccumulation of cadmium in freshwater fish: An environmental perspective. Insight Ecol., 4(1): 1-12. https://doi.org/10.5567/ECOLOGY-IK.2015.1.12

Piotrowska, A., Mlyni, K., Siwek, A., Dybala, M., Opoka, W., Poleszak, E. and Nowak, G., 2008. Antidepressant-like effect of chromium chloride in the mouse forced swim test: Involvement of glutamatergic and serotonergic receptors. Pharmacol. Rep., 60: 991-995.

Pyle, G. and Wood, C., 2008. Radiotracer studies on waterborne copper uptake, distribution, and toxicity in rainbow trout and yellow perch: A comparative analysis. Hum. Ecol. Risk. Assess., 14: 243–265. https://doi.org/10.1080/10807030801934994

Qadir, A. and Malik, R.N., 2011. Heavy metals in eight edible fish species from two polluted tributaries (Aik and Palkhu) of the River Chenab, Pakistan. Biol. Trace Elem. Res., 143: 1524-1540. https://doi.org/10.1007/s12011-011-9011-3

Rahman, Z., Ahmad, I. And Rashid, I.,. 2018. Effects of cadmium exposure on growth and survival and accumulation in various organs of Nile Tilapia (Oreochromis niloticus, Linnaeus). J. Agri. Aquacult., 1: 1-10.

Rauf, A., Javed, M., Ubaidullah, M. and Abdullah, S., 2009. Heavy metal levels in three major carps (Catla catla, Labeo rohita, Cirrhina mrigala) from the river Ravi, Pakistan. Pak. Vet. J., 29: 24-26.

SMEWW, 1989. Standard Methods for the Examination of Water and Wastewater. (17th Ed.). A.P.H.A. Washington, DC.

Shaheen, T. and Jabeen, F., 2015. Effect of various doses of Cr (VI) on survival and growth of Cyprinus carpio. Pakistan J. Zool., 47: 913-919.

Sherwood, G.D., Rasmussen, J.B., Rowan, D.J., Brodeur, J. and Hontela, A., 2000. Bioenergetic costs of heavy metal exposure in yellow perch (Perca flavescens): In situ estimates with a radiotracer technique. Can. J. Fish. Aquat. Sci., 57: 441-450. https://doi.org/10.1139/f99-268

Steel, R.G.D., Torrie, J.H. and Dickey, D.A., 1996. Principles and procedures of statistics: A Biometrical Approach (3rd Ed.). McGraw Hill Book Co, Singapore, pp. 627.

Stout, M.D., Herbert, R.A., Kissling, G.E., Collins, B.J., Travlos, G.S., Witt, K.L., Melnick, R.L., Abdo, K.M., Malarkey, D.E. and Hooth, M.J., 2009. Hexavalent chromium is carcinogenic to F344/N rats and B6C3F1 mice after chronic oral exposure. Environ. Health Perspect., 117: 716-722. https://doi.org/10.1289/ehp.0800208

Subathra, S. and Karuppasamy, R., 2007. Toxic effects of copper on bioenergetics and growth rates in fingerlings and adult stage of the fish, Mystus vittatus. J. Fish. Aquat. Sci., 2: 285-293. https://doi.org/10.3923/jfas.2007.285.293

., . and ., 2003. Effect of a heavy metal model mixture on biological parameters of rainbow trout Oncorhynchus mykiss. , 10: 103-107. https://doi.org/10.1065/espr2002.02.109

Witeska, M. and Jezierska, B., 2003. The effects of environmental factors on metal toxicity to fish (Review). Fresen. Environ. Bull., 12: 824-829.

Yaqub, S., 2012. Studies on the determination of acute and lethal toxicities of waterborne and dietary metals in fish. Ph.D. thesis, Department of Zoology and Fisheries, University of Agriculture, Faisalabad, Pakistan. pp.107.

Zhao, S., Feng, C., Quan, W., Chen, X., Niu, J. and Shen, Z., 2012. Role of living environments in the accumulation characteristics of heavy metals in fishes and crabs in the Yangtze River Estuary, China. Mar. Poll. Bull., 64:1163-1171. https://doi.org/10.1016/j.marpolbul.2012.03.023

To share on other social networks, click on any share button. What are these?

Punjab University Journal of Zoology

June

Vol.39, Iss. 1, Pages 01-134

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe