LETHAL DISSOLVED OXYGEN AND BLOOD PROPERTIES OF GREY MULLETS Mugil cephalus IN SEAWATER AND FRESHWATER [Oksigen Terlarut Letal dan Gambaran Darah Ikan Belanak Mugil cephalus di Air Laut dan Tawar]

Vitas Atmadi Prakoso, Ki Tae Kim, Byung Hwa Min, Rudhy Gustiano, Young Jin Chang
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Abstract

Ikan belanak Mugil cephalus adalah salah satu spesies ikan euryhaline dan merupakan ikan ekonomis penting yang terdistribusi secara luas di dunia. Namun, penelitian tentang pengaruh faktor lingkungan terhadap metabolisme ikan ini masih kurang banyak diteliti meskipun hal tersebut penting untuk mengoptimalkan budidaya. Karena itu, penelitian ini dilakukan untuk mempelajari tingkat oksigen terlarut (DO) letal dan gambaran darah ikan belanak pada kondisi pemeliharaan dengan salinitas berbeda. Dua kelompok penelitian dilakukan untuk mengukur kadar DO letal dan gambaran darah ikan belanak pada kondisi pemeliharaan di air laut (LOS) dan air tawar (LOF). Pengamatan dilakukan menggunakan closed rectangular chamber dan sampel darah. Hasil penelitian menunjukkan bahwa kondisi ikan belanak menjadi tidak stabil pada kondisi oksigen terlarut di bawah 2 mg/L (1.3 mg/L pada LOS, 1.6 mg/L pada LOF). Dalam kondisi oksigen terlarut menjadi 1 mg/L, aktivitas ikan menurun dan mengalami kematian pada konsentrasi 0.3 mg/L. Kedua kelompok penelitian yang diamati tidak berbeda nyata (P>0.05). Parameter darah seperti Ht, Hb, osmolalitas, kortisol, dan glukosa dalam percobaan LOS memiliki nilai yang lebih tinggi dibandingkan dengan LOF. Percobaan menunjukkan bahwa indikator respon stress pada ikan belanak semakin meningkat dengan menurunnya kandungan oksigen dalam air. Kadar kortisol berada pada nilai 90.7 ng/ml di LOS dan 56.4 ng/ml di LOF, sedangkan kadar glukosa berada pada nilai 169.0 ng/ml di LOS dan 71.5 ng/ml di LOF. Dari penelitian ini dapat disimpulkan bahwa kadar oksigen terlarut bagi ikan belanak dianjurkan tidak berada di bawah 2 mg/L pada kondisi pemeliharaan di air laut maupun air tawar untuk menghindari kematian pada ikan.

Keywords

Oksigen, letal, gambaran darah, Mugil cephalus.

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References

Brett JR. 1979. Envir onmental Factor s and Gr owth. In: Fish Physiology, Vol. VIII, Bioenergetics and Growth. WS Hoar, DJ Randall and JR Brett (Eds), Academic Press, New York.

Chang YJ, MH Jeong, BH Min, WH Neill and LP Fontaine. 2005. Effect of Photoperiod, Temperature, and Fish Size on Oxygen Consumption in the Black Porgy A canthopagrus schlegeli. Journal of Fisheries Science and Technology 8, 142-150.

Dalla Via D, G van den Thillart, O Cattani and P Cortesi. 1998. Behavioural Responses and Biochemical Correlates in Solea solea to Gradual Hypoxic Exposure. Canadian Journal of Zoology 76, 2108–2113.

Duan Y, X Dong, X Zhang and Z Miao. 2011. Effects of Dissolved Oxygen Concentration and Stocking Density on the Growth, Energy Budget and Body Composition of Juvenile Japanese Flounder, Paralichthys olivaceus (Temminck et Schlegel). A quaculture Resources 42, 407-416.

Effendie MI. 1984. Penilaian Per kembangan Gonad Ikan Belanak Liza subviridis Valenciennes di Perairan Muara Sungai Cimanuk, Indramayu bagi Usaha Pengadaan Benih. Disertasi. Institut Pertanian Bogor, Bogor.

Franklin CE, IA Johnston, T Crockford and C Kamunde. 1995. Scaling of Oxygen Consumption of Lake Magadi Tilapia, a Fish Living at 37°C. Journal of Fish Biology 46, 829-834.

Itazawa Y. 1959. Gas Content of the Blood in Response to that of Medium Water in Fish. Comparison of the Response in Several Species. Bulletin of the Japanese Society of Scientific Fisheries 25, 301-306.

Iwama GK, A Takemura and K Takano. 1997. Oxygen Consumption Rates of Tilapia in Freshwater, Seawater, and Hypersaline Seawater. Journal of Fish Biology 51, 886- 894.

Jeong MH, YS Kim, BH Min and YJ Chang. 2007. Effect of Fish Number in Respiratory Chamber on Routine Oxygen Consumption of Black Porgy A canthopagrus schlegeli Reared in Seawater or Freshwater. A quaculture 20, 121-126.

Kim IN, YJ Chang and JY Kwon. 1995. Patter n of Oxygen Consumption in Six Species of Marine Fish. Journal of the Korean Fisheries Society 28, 373-381.

Kucuk S, A Karul, S Yildirim and K Gamsiz. 2013. Effects of Salinity on Growth and Metabolism in Blue Tilapia (Oreochromis aureus). African Journal of Biotechnology 12, 2715-2721.

Kutty MN and MP Mohamed. 1975. Metabolic Adaptations of Mullets Rhinomugil corsula Hamilton with Special Reference to Energy Utilization. A quaculture 5, 253-270.

Lefrancois C and G Claireaux. 2003. Influence of Ambient Oxygenation and Temperature on Metabolic Scope and Scope for Heart Rate of the Sole (Solea solea). Marine Ecology Progress Series 259, 273-284.

Lovell T. 1998. Nutrition and Feeding of Fish. Second Edition. Kluwer Academic Publications, Massachusetts.

Mallya YJ. 2007. The Effects of Dissolved Oxygen on Fish Growth in Aquaculture. UNU-Fisheries Training Programme, Reykjavik.

Matthews KR and NH Berg. 1997. Rainbow Tr out Responses to Water Temperature and Dissolved Oxygen Stress in Two Southern California Stream Pools. Journal of Fish Biology 50, 50-67.

Porchas MM, LRM Cordova and RR Enriquez. 2009. Cortisol and Glucose: Reliable Indicators of Fish Stress?. Pan American Journal of Aquatic Sciences 4, 158-178.

Randall D. 1982. The Control of Respiration and Circulation in Fish during Exercise and Hypoxia. Journal of Experimental Biology 100, 275-288.

Saleh M. 2008. Captur e-based Aquaculture of Mullets in Egypt.In: Capture-based Aquaculture. Global Overview. A Lovatelli and PF Holthus (Eds). 109-126. FAO FisheriesTechnical Paper No.508. FAO. Rome.

Schurmann H and JF Steffensen. 1992. Lethal Oxygen Levels at Different Temperatures and The Preferred Temperature During Hypoxia of the Atlantic Cod Gadus morhua L. Journal of Fish Biology 41, 927-934.

Shepard MP. 1955. Resistance and Toler ance of Young Speckled Trout Salvelinus fontinali to Oxygen Lack with Special Reference to Low Oxygen Acclimation. Journal of the Fisheries Research Board of Canada 12, 3.

Smith KJ and KW Able. 2003. Dissolved Oxygen Dynamics in Salt Marsh Pools and Its Potential Impacts on Fish Assemblages. Marine Ecology Progress Series 258, 223-232.

Sulistiono, M Arwani and KA Aziz. 2001. Gr owth of Mullet, Mugil dussumieri in Ujung Pangkah, East Java. Jurnal Iktiologi Indonesia 1, 31-37.

Sylvester JR. 1975. Cr itical Ther mal Maxima of Thr ee Species of Hawaiian Estuarine Fish: A Comparative Study. Journal of Fish Biology 7, 257-262.

Szczepkowski M, B Szczepkowska and I Piotrowska. 2011. Impact of Higher Stocking Density of Juvenile Atlantic Sturgeon, A cipenser oxyrinchus Mitchill, on Fish Growth, Oxygen Consumption, and Ammonia Excretion. Archives of Polish Fisheries 19, 59-67.

Thurston RV, GR Phillips and RC Russo. 1981. Incr eased Toxicity of Ammonia to Rainbow Trout (Salmo gairdneri) Resulting from Reduced Concentrations of Dissolved Oxygen. Canadian Journal of Fisheries and Aquatic Sciences 38, 983-988.

Tsuzuki MY, CA Strussmann and F Takashima. 2008. Effect of Salinity on The Oxygen Consumption of Larvae of the Silversides Odontesthes hatcheri and O. bonariensis (Osteichthyes, Atherinopsidae). Brazilian Archives of Biology and Technology 51, 563-567.

Wahyudewantoro G and Haryono. 2013. Hubungan Panjang Berat dan Faktor Kondisi Ikan Belanak Liza Subviridis di Perairan Taman Nasional Ujung Kulon-Pandeglang, Banten. Bionatura-Jurnal Ilmu-ilmu Hayati dan Fisik 15, 31-37.

Weithman AS and MA Haas. 1984. Effects of Dissolved Oxygen Depletion on the Rainbow Trout Fishery in Lake Taneycomo, Missouri. Transactions of the American Fisheries Society 113, 109-124.

Zaki MS, SO Mostafa, OM Fawzi, M Khafagy and FS Bayumi. 2009. Clinicopathological, Biochemical and microbiological Change on Grey Mullets Exposed to Cadmium Chloride. American-Eurasian Journal of Agricultural and Environmental Sciences 5, 20-23.


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