1 ANALYSIS OF GROWTH, PROXIMATE AND TOTAL ENERGY OF SANDFISH HOLOTHURIA SCABRA CULTURED AT DIFFERENT CULTIVATED HABITAT 1) Ambo Tuwo1), Joeharnani Tresnati1) dan Saharuddin2) Faculty of Marine Science and Fisheries, Hasanuddin University 2) Postgraduate Program, Hasanuddin University ABSTRACT The problem in the sea cucumber culture development in Indonesia is the difficulty to find the culture area that could provide optimal production. This study analyzed the cultivated habitat that could provide optimal growth, proximate and total energy to sandfish Holothuria scabra cultivated in different habitats. The study was done from March to June 2011 in the Puteangin Island, Lasitae Village, District Tanete Rilau, Barru Regency, South Sulawesi. The cage size used was 2 m in length, 1 m in width, and 1.5 m in height. The net mesh-size was 0.5 inch. The cage placed at three different habitats, i.e. sandy overgrown with seagrass habitat, sandy covered with corals habitat, and sandy habitat. The study consisted of three treatments and three replications. Growth was observed by measuring the daily specific growth rate and absolute weight growth. Proximate and energy content of sandfish was analyzed at the beginning and the end of the study. The study reveals that the sand and seagrass habitat provide the best results with daily specific growth rate is 1.15% ± 0.03%. The absolute weight growth is 28.45 g ± 0.95 g. The proximate content is 0.24 g ± 0.492 g for protein, 0.07 g ± 0.395 g for fat, and 18.026 g ± 0.39 g for carbohydrate. The highest energy content is 176 997 calories. INTRODUCTION In Indonesia, there are 23 species of sea cucumbers, which 5 species have important economic value. Sandfish Holothuria scabra is the species most widely traded (Hartati et al. 2004). Sea cucumbers could be found in the coastal waters, ranging from tidal areas to deep water. Sea cucumbers prefer clear waters in the sheltered area. Sandfish are frequently found in the sandy or muddy areas overgrown with seagrass (Radjab, 2002). The scientific classification of sandfish is : Kingdom : Animalia; Phylum : Echinodermata; Class : Holothuroidea; Order : Aspidochirotida; Family : Holothuriidae; Genus : Holothuria; subgenus Metriatyla; Species : Holothuria scabra. The synonyms is Holothuria albida Savigny, 1867; Holothuria gallensis Pearson, 1903; Holothuria saecularis Bell, 1887. Sandfish is greyish-black on the upper side with dark-coloured wrinkles but paler on the underside. It is a medium-sized species, to 400 cm long, It is broader than it is high and has a pliable skin. Spicules are well developed tables and knobbed buttons. Sandfish can be found on reefs and in in shallow water on soft sediments or sea-grass flats (Guille et al, 1986; MSIP, 2011); it may be exposed or partially buried in sand. Sandfish is found throughout the Indo-Pacific region from East Africa to the Eastern Pacific. They are usually found between the latitude 30 oN and 30 oS (Agudo, 2006). Sea cucumber is nutritious seafood with a high protein and low lipid content and is rich in gluten, nitrogen, iodine and other nutritional elements (Wang, 1997). Sea 2 cucumbers used as a food contains high nutrient value, i.e. 43.1% protein, 2.2% fat, 27.1% moisture, 27.6% ash content (Rustam, 2006 dan Hendri et al. 2008). The amino acids of sandfish are generally the essential amino acids (Chen, 2004). Sandfish is a high economic value commodity and has a good prospect of domestic and international market. The domestic price could reach Rp.900.000 per kilogram (Hartati et al. 2005). Sandfish is the most expensive sea cucumber produced in tropical and sub tropical area. The price of dried product or trepang ranges from 25 to 63 US$ kg-1, it depends on grade and quality. The grade is related to the thickness of the body wall and size. Generally, there are three grading size of sandfish dried product, i.e. grade A for 10 to 30 pc kg-1; grade B for 15 to 40 pc kg-1; and grade C for more than 40 pc kg-1. The grade A price is range from 43 to 63.0 US$ kg-1; grade B is range 35 to 40 US$ kg-1; and grade C is range 25 to 37 US$ kg-1 (Anom. 2001a; Anom. 2001b Anom. 2002a; Anom. 2002b). The pularity of sea cucumber as a health food purportedly able to cure arthritis and some types of cancer, other forms of high value processed sea cucumbers are expected to receive good market acceptance and preference in local and international markets. Sandfish yield is one of the largest sea cucumber catches worldwide; and it is an important source of income for marginal fishers in impoverished coastal villages in Southeast Asia countries. Sandfish are highly exploited so that it population continues to decline in the wild (Sudjiharno, 2003). To maintain the sustainability of sandfish production is needed. In Southeast Asian countries, cultivation has carried only on sandfish. Sandfish is better than another because of its high prices, also has a better environment adaptation than other sea cucumber species, such as more resistant to salinity fluctuation than other sea cucumbers species. Sandfish cultivation is generally located in shallow coastal areas; water depth should be 75 to 100 cm (Tuwo, 2004). Increasing sandfish production could not be done by only relying on wild capture. Sandfish production needs to be done both wild capture and cultivation. Actually, sandfish cultivation faces many problems, i.e. sandfish adaptation to the cultivation area. One problem often encountered sandfish cultivation area is the lower growth rate and lower nutritional value of sandfish from cultivation compare to sandfish from the wild. To overcome this problem is needed to find out the cultivation area that has environment condition to sandfish natural habitat. Until present, there has been no previous research on the sandfish habitat condition that favorable to sandfish cultivated growth. This study aims to analyzed the habitat condition that could potentially provide better growth rate and. METHODS The study was conducted from March to June 2011 in the island Puteangin, Lasitae Village, District Tanate Rilau, Barru regency, South Sulawesi. There are 100 individuals used in this study. The sandfish weight is 28 to 29 g of as many as 100 individuals. Cultivation media used in this study were the nets that have length, width and height of each of the 2 x 1 x 1.5 m. the nets size is of 0.5. The study consisted of three treatments and each treatment consisted of three replications. Thus, this study consists of nine units of the experiment. The treatments tested were the bottom waters are: (1) sandy overgrown with seagrass habitat, (2) sandy covered with corals habitat, (3) sandy habitat 3 Parameters measured were survival rate, growth, proximate (proteins, fats, carbohydrates) and total energy. The survival rate (SR, %) is calculated using the formula Effendie (1979): SR = Nt / No x 100; wherein SR is the survival rate (%), Nt is the number of sandfish at the end of the study, No is the number of sandfish at the beginning of the study. The daily specific body growth rate (SGR) was calculated using the formula Effendie (1979): SGR = {(lnWt - lnWo) / t} x 100, wherein the Wt is the average weight of the end of the study (g), Wo is the average weight at the beginning of the study (g), t is the duration of the study (days). The absolute weight growth was calculated using the formula Effendie (1979): W = Wt - Wo; wherein Wt is the average weight at the end of the study, and Wo is the average weight at the beginning of the study. Proximate analysis (protein, fat, carbohydrates) and total body energy was measured at the beginning and end of the study. Environmental parameters observed were phytoplankton, macro benthos, sediment type, salinity, temperature, dissolved oxygen, and nitrate. RESULTS AND DISCUSSION Survival Rate The survival rate of sandfish was 40% to 70%. Highest survival rate was found at Sandy overgrown with seagrass habitat, which was 70% (average 66.67%). The lowest survival rate was found at habitat sandy, which was 40% (average 50.00%). Sandfish survival rates were significantly different two types of habitat, the sandy overgrown with seagrass habitat and sandy covered with corals habitat (Table 1). The sandfish survival rates obtained in this study is higher than the results of other studies. Hair (2011) reveals that the survival rate of sandfish after six months rearing was around 28%; and the highest survival rate was 41%, recorded from a pen of large sandfish. Table 1. Survival rate of sandfish (Holothuria scabra) cultivated at three different types of habitats. Habitat Survival Rate (%) Sandy and seagrass 66.67 ± 5.77a Sandy and coral 56.67 ± 5.77b Sandy 50.00 ± 10.00b tcount tA&B=2.123; tA&C=2.501; tB&C=1.001 ttable 0.134 Growth Rate The highest daily specific body growth rate (1.15) and absolute weight growth (28.45) of sandfish were found at sandy overgrown with seagrass habitat. The two growth parameters of sandfish were significantly different in the three types of habitats. Both growth parameters is greater than the second 4 Table 2. Daily specific body growth rate and absolute weight growth of sandfish (Holothuria scabra) cultivated at three different types of habitats. Habitats Daily Specific Growth Rate (%) Absolute Weight Growth (g) Sandy and seagrass 1.15 ± 0.03a 28.45 ± 0.95a Sandy and coral 0.83 ± 0.01b 18.51 ± 0.28b Sandy 0.62 ± 0.04c 12.97 ± 1.03c tcount tA&B=17.270; tA&C=18.358; tB&C=8.823 tA&B=17.308; tA&C=19.093; tB&C=8.986 ttable 0.134 0.134 Proximate and Total Energy During the cultivation, protein, fat, carbohydrate and total energy increased. The protein, fat, carbohydrate and total energy were significantly different in the three types of habitat (Table 3). The highest content of protein, fat, carbohydrate and total energy of sandfish were found at sandy overgrown with seagrass habitat. While the lowest were found in sandy habitat, except for the fat. Table 3. Increase of protein, fat, carbohydrate and energy of sandfish (Holothuria scabra) cultivated at three different types of habitats. Habitat Protein (g) Fat (g) Carbohydrate (g) Total Energy (cal) Sandy and seagrass 9.49 + 0.09a 0.40 + 0.07a 18.03 + 0.39a 177.00 + 42.60a Sandy and coral 8.25 + 0.24b 0.09 + 0.08b 1.88 + 0.01b 70.50 + 5.04b Sandy 6.82 + 0.32c 0.13 + 0.16b 1.38 + 0.12c 8.85 + 5.75c tcount tA&B=8.379; tA&C=13.918; tB&C=6.193 tA&B=5.051; tA&C=2.677; tB&C=0.387 tA&B=71.701; tA&C=70.671; tB&C=7.194 tA&B=4.300; tA&C=6.775; tB&C=17.975 ttable 0.134 0.134 0.134 0.134 There were 23 macro benthos species found at the three types of sandfish cultivation habitat, namely: Anadara maculosa, Anomalodiscus sguamosus, flat worms, Chantarus elegipangans, Cerastoderma adule, Ceritium ruppellii, Ceritium vulgatum, Ceritium sp, Codakia orbicularis, Conus sp., Donax sp., Hindsia magnifica, Isognomon isognomon, Crab, Lopha cristagalli, Patellar barbata, Penion mandarinus, Rhinoclavis asper, Rhinoclavis sp., Spisula elliptica, Trisidos tortuosa, Turitella sp., and Xhenophora pallidula. Each habitat type has macro benthos indicator. Chantarus elegans, flat worms, Penion mandarinus and Rhinoclavis sp could be the macro benthos indicator for sandy overgrown with seagrass habitat. Anadara maculosa, Cerastoderma adule, Ceritium ruppellii, Ceritium vulgatum, Isognomon isognomon, Lopha cristagalli and Trisidos tortuosa could be the macro benthos indicator for sandy covered with corals habitat. While Conus sp., Patellar barbata, Rhinoclavis asper, and Turitella sp 5 could be the macro benthos indicator for sandy covered with corals habitat. The macro benthos that occupied the three habitat types were Spisula elliptica, Donax sp., and Anomalodiscus sguamosus (Table 4). Although each habitat type has macro benthos indicator, but the survival rate difference of sandfish found in this study could not show the direct relation between the survival rate and macro benthos, even though the present of crabs. Likewise, the differences in growth, protein, fat, carbohydrate and total energy of sandfish could not be related directly to the macro benthos species. Macro benthos could be a sandfish competitor in terms of space and food, but the impact of this competition could not be revealed in this study. It still needs further observation. Table 4. The macro benthos found at three types of habitat cultivated by sandfish (Holothuria scabra). No. Macro benthos 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21. 22. 23. Chantarus elegans Flatworms Penion mandarinus Rhinoclavis sp. Xhenophora pallidula Codakia orbicularis Crab Ceritium sp Spisula elliptica Donax sp. Anomalodiscus sguamosus Hindsia magnifica Anadara maculosa Cerastoderma adule Ceritium ruppellii Ceritium vulgatum Isognomon isognomon Lopha cristagalli Trisidos tortuosa Conus sp. Patella barbata Rhinoclavis asper Turitella sp. Sandy and seagrass Average Std 15.00 9.67 9.67 7.33 3.67 3.67 2.00 8.00 25.33 4.67 7.33 33.33 - 4.36 4.62 0.58 0.58 3.21 0.58 1.73 0.00 7.09 0.58 6.43 7.64 - Sandy and coral Average 18.33 5.67 7.00 10.33 8.00 6.67 25.67 14.67 2.33 16.67 11.67 - Std 16.07 0.58 0.00 17.90 1.00 0.58 1.15 4.51 2.08 5.77 2.89 - Sandy Average 10.67 7.00 5.00 1.33 9.33 2.67 1.67 4.33 3.33 8.33 3.33 Std 9.29 2.00 2.65 1.15 1.15 0.58 1.53 1.15 0.58 0.58 0.58 There are six phytoplankton species were found at three cultivation habitats, namely: Ceratium furca, Cetoceros sp, Dinophysis sp, Gimnodium sp, Oscillatoria sp, Pleurosigma sp. The six phytoplankton species were commonly found in three cultivation habitat. Ceratium furca tend to be more prevalent in sandy habitat is overgrown with grass. Gimnodium sp more prevalent in the sandy overgrown with seagrass habitat. Gimnodium sp, Cetoceros and Pleurosigma were two phytoplankton species that often found in sandy covered with corals habitat and sandy habitat. Cetoceros and Pleurosigma are two types of phytoplankton were often found in three cultivation habitat (Table 5). Phytoplankton composition could not to be a strong reason 6 to explain the differences in content of protein, fat, carbohydrate and total energy at every cultivation habitats. Table 5. Phytoplankton found at three types of habitat cultivated by sandfish (Holothuria scabra). No. 1. 2. 3. 4. 5. 6. Phytoplankton Dinophysis sp Cetoceros Pleurosigma sp Gimnodium sp Oscillatoria sp Ceratium furca Sandy and seagrass Average Std 12.33 10.79 225.00 91.24 19.00 5.29 6.00 3.61 7.00 1.00 17.67 11.02 Sandy and coral Average Std 115.33 6.43 13.67 9.87 15.67 5.13 5.00 2.00 3.33 2.89 Sandy Average Std 4.33 3.79 82.33 27.39 14.33 5.13 20.00 4.36 3.67 6.35 - The soil fraction was same at three cultivation habitats. The texture type was sandy (Table 6). This sediment texture is suitable for sandfish cultivation habitat. Gultom (2004) revealed that soil fraction suitable for sandfish is 83.62% - 93.40% of sand fraction, 0.57% - 2.17% of dust and 3.20% - 5.68% of clay. Naturally, sea cucumbers live in sandy areas mixed with rubble and overgrown grass (Gultom, 2004). Chen (2004) and Agudo (2006) reveal that sandfish suitable reared at substratum muddy or sandy bottom, preferably with seagrass; and depth range from 3 to 10 meters (Chen, 2004; Agudo, 2006). The content of nitrogen, phosphorus, pH, organic matter and sediment were relatively same for the three cultivation habitats. The pH was around 8. The ideal conditions for a desirable cultivation site of sandfish should be pH range from 7.9 to 8.4 (Chen, 2004). Soil organic matter content was slightly higher in the sandy overgrown with seagrass habitat and sandy covered with corals habitat (Table 6). Mercier et al, (1999) and Pitt and Duy (2004) found that sandy muddy substrates were rich in organic matter. The content of nitrogen, phosphorus, pH, organic matter at the three cultivation habitats was feasible for sandfish. Salinity is one of important factors for the sandfish growth. Salinity waters during this study ranged from 27 to 31 ppt (Table 7). This range is feasible for the cultivation of sandfish. Rusyani et al. (2003) found that the ideal seawater salinity range for sandfish was 28 to 33 ppt. The ideal conditions for a desirable site are salinity range from 28 to 31 (Chen, 2004; Agudo, 2006). Sandfish tended to burrow when salinity decreased, whereas increased water temperatures reduced normal burrowing behavior (Mercier et al, 2000a, 2000b). Temperature has an important role for the sandfish growth. Water temperature during this study ranged from 28 to 32 oC. Optimum temperature for the sea cucumber is 24 to 30oC (Martoyo et al, 2006; Chen, 2004; Agudo, 2006). Dissolved oxygen concentration during this study was 3.5 to 8.5. The optimum dissolved oxygen concentration for the cucumbers ranged from 4 to 8 ppm (Martoyo et al, 2006). The content of nitrate (NO3) obtained during the study ranged from 0.02 to 0.08 ppm. This concentration is still suitable for the survival and growth of the sea cucumber. 7 Table 6. Chemical and physical parameters of three habitats cultivated by sandfish (Holothuria scabra). No. Sandy and seagrass Average Std Contents Sandy and coral Average Std Sandy Average Std Beginning 0.067 0.003 0.062 0.006 0.026 0.004 End 0.072 0.003 0.069 0.004 0.032 0.004 Beginning 6.521 0.004 7.525 0.234 6.388 0.005 End 6.521 0.004 7.525 0.234 6.388 0.005 Beginning 8.180 0.020 8.267 0.124 8.493 0.025 End 8.197 0.015 8.293 0.093 8.493 0.012 Beginning 0.886 0.003 0.894 0.010 0.440 0.145 End 0.958 0.014 0.955 0.016 0.430 0.102 Sand (%) 92.00 - 96.00 - 93.00 - Dust (%) 5.00 - 3.00 - 4.00 - Clay (%) 3.00 - 1.00 - 3.00 - Sandy - Sandy - Sandy - 1. N (%) 2. P (ppm) 3. pH 4. BO (%) 5. Sediment Texture types Table 7. Water quality parameters at three types of habitat cultivated by sandfish (Holothuria scabra). Water Quality Salinity (ppt) Temperature (oC) DO (ppm) Nitrate (ppm) Sandy and seagrass 27 - 31 28 - 32 3.667+0.006 - 8.527+0.031 0.040+0.000 - 0.07+0.006 Sandy and coral 27 - 31 28 - 32 3.750+0.044 - 8.157+0.040 0.040+0.000 - 0.067+0.006 Sandy 27 - 31 28 - 32 3.473+0.025 - 8.660+0.017 0.033+0.006 - 0.067+0.006 Habitat CONCLUSION The study reveal that survival rate, growth, proximate and total body energy content of sandfish found in sandy habitats overgrown grass is better that the two other cultivation habitat. The lowest levels found in sandy habitats. REFERENCES Agudo, N.S. 2006. Sandfish Hatchery Techniques. Noumea, New Caledonia: Secretariat of the Pacific Community. 44 p. 8 Anom. 2001a. Papua New Guinea Export Prices of Beche-de-mer. SPC Beche-de-Mer Info. Bull. No. 15: 30 Anom. 2001b. Beche-de-mer Prices on the Asian Markets (January–July 2001). 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