Int. J. Aquat. Biol. (2017) 5(6): 408-412 DOI: ISSN: 2322-5270; P-ISSN: 2383-0956 Journal homepage: www.ij-aquaticbiology.com © 2017 Iranian Society of Ichthyology Short Communication Length-weight relationship of black sea urchin (Stomopneustes variolaris) in Sri Lanka Heethaka Krishantha Sameera De Zoysa*1, 2, Bedigama Kankanamge Kolitha Kamal Jinadasa3, Edirisinghe Mudiyanselage Ranjith Keerthi Bandara Edirisinghe2, Gabadage Dona Thilini Madurangika Jayasinghe3 1Department of Food Technology, Faculty of Technology, Rajarata University of Sri Lanka, Mihintale, Sri Lanka. 2Department of Physical Sciences, Faculty of Applied Sciences, Rajarata University of Sri Lanka, Mihintale, Sri Lanka. 3Institute of Post-Harvest Technology (IPHT), National Aquatic Resources Research and Development Agency (NARA), Colombo, Sri Lanka. Article history: Received 6 June 2017 Accepted 24 December 2017 Available online 2 5 December 2017 Keywords: Indian Ocean Echinodermata Biology Sea Urchin Abstract: This study attempted to describe the length and weight frequency, and length-weight relationship in the black sea urchin, Stomopneustes variolaris, in Sri Lanka. The sampling sites Mount-Lavinia (n=43), Beruwala (n=99) and Tangalle (n=55) were selected from South-west coast in Sri Lanka. The shell length and body weight were measured separately for three sampling sites. The mean length and weight of S. variolaris were 5.55±1.04 cm, 101.40±57.76 g; 6.54±0.86 cm, 147.90±50.40 g, and 6.41±1.05 cm, 150.50±59.45 for Mount-Lavinia, Beruwala and Tangalle, respectively. In addition, the length-weight relationship of S. variolaris were W=0.9953*L2.6472, W=0.9651*L2.6536 and W=1.4665*L2.4637 for Mount-Lavinia, Beruwala and Tangalle, respectively. Introduction The black sea urchin (Stomopneustes variolaris) (Fig. 1) is one of the warm water species found in the Indian Ocean. They belong to the family Stomopneustidae and are distributed in the tropical and subtropical regions of the Indo-Pacific from the East African coast to Samoa and to the Bonin Islands to the north (Giese et al., 1964). They are omnivores feeding mainly on algae and seaweeds. Distribution of S. variolaris is limited to a depth up to 18 m (Giese et al., 1964; James, 1982; Kroh, 2014). Of the 28 species of sea urchins found in Sri Lankan seas (Jayakody, 2012), S. variolaris is highly restricted in distribution to the Western and Southern coastal areas (De Zoysaa et al., 2016; Jinadasa et al., 2016). In biological aspects, the growth rate of sea urchins and natural mortality mainly depend on temperature and food availability (Reynolds and Wilen, 2000). Sea urchins accumulate nutrients in the gonads, which is a highly economically important delicacy in the world (James and Siikavuopio, 2011; Salon, 1985; Scheibling and Mladenov, 1987). According to James (1983), this species is the most abundant edible *Corresponding author: Heethaka Krishantha Sameera De Zoysa DOI: https://doi.org/10.22034/ijab.v5i6.304 E-mail address: dezoysahks@yahoo.com species found in the Indian Ocean such as Lakshadweep Islands, Andaman Islands and Sri Lanka. Apart from the few studies done on the diversity, abundance and their distribution (Jayakody, 2012), very little is known about the biology of Sri Lankan sea urchins. Therefore, this study was conducted to examine the length-weight relationships of the common sea urchin, S. variolaris in Sri Lanka. Materials and Methods A total of 197 individuals were collected from rocky reefs in Mount-Lavinia (n=43), Beruwala (n=99) and Tangalle (n=55) (Fig. 2) in 2014. All collected individuals were transported to the Institute of Post- Harvest Technology (IPHT), National Aquatic Resources Research and Development Agency (NARA). After that, the total body weights of all specimens were weighed to the nearest 0.01 g. The length of the sea urchin body was determined by measuring horizontal test diameter twice in right angles to the nearest 0.02 mm in all the specimens using a vernier caliper and the two measurements were averaged to obtain the diameter. 409 Int. J. Aquat. Biol. (2017) 5(6): 408-412 The length-weight relationship was calculated using the W=aLb equation and after logarithmically transferred form Log W=Log a b Log L. Where W is the weight in g, L is the total length cm, ‘a’ is the intercept and b are the slope. Both of a and b were estimated by using the linear regression analysis (Le Cren, 1951). All the data were analysed by using the Minitab 16.0 version and the Microsoft Excel 2010 version. Results Weight and Average Shell Length frequency distribution: The most common shell length in the sample from Mount-Lavinia reef was 5.4 cm with an average of 5.55±1.04 cm (Fig. 3). The most frequent total body weight in the Mount-Lavinia reef sample was 80 g and the average weight of the sample was and 101.40±57.76 g (Fig. 4). For the Beruwala reef, the commonest shell length was 6.5 cm with the average of 6.54±0.86 cm (Fig. 5) and most frequent weight was 160 g with the average of 147.90±50.40 g (Fig. 6). The Tangalle reef population 6.5 cm was most frequent shell length while the average was 6.41±1.05 cm (Fig. 7) and the most frequent total body weight was 150g with an average of 150.50 ± 59.45 g (Fig. 8). Length-weight relationships (LWR): There was a significant correlation between S. variolaris shell length and total body weight (P<0.05) for all three sampling sites (Figs. 9, 11, 13). There was significant linear correlation between logarithmic values of shell length and total body weight (P<0.05) for all three sampling sites for S. variolaris (Figs. 10, 12, 14, Table 1). Discussion The frequency distribution of shell length and weight of S. variolaris reveals that the shell length ranges from 3.30 to 8.90 cm and weight from 30.15 to 346.56 g for all the studied populations. But according to the Smith and Kroh (2011), S. variolaris from Visakhapatnam Coast (India) has a maximum shell length of 11 cm. This is the first time a study has been conducted in Sri Lanka to determine the LWR of S. variolaris. In fisheries research, the LWR is used as a good indicator, because it gives an idea about well-being, Figure 1. Stomopneustes variolaris. Figure 2. Sampling sites of Stomopneustes variolaris. 410 De Zoysa et al. / Length-weight relationship of black sea urchin in Sri Lanka maturity, the rate of feeding and the rate of growth of a particular species (Le Cren, 1951; Rahman et al., 2012). The value of the exponent (b) determine whether the growth isn weight is isometric (b=3) or Figure 3. Shell length frequency distribution at Mount-Lavinia reef. Figure 4. Weight frequency distribution at Mount-Lavinia reef. Figure 5. Shell length frequency distribution at Beruwala reef. Figure 6. Weight frequency distribution at distribution at Beruwala reef. Figure 7. Shell length frequency distribution at Tangalle reef. Figure 8. Weight frequency distribution at Tangalle reef. Table 1. Length-weight relationships and other parameters of Stomopneustes variolaris at selected sites Locations Length-weight relationships (Log W = Log a + b Log L) a b W r2 Mount- Lavinia y = - 0.0047 + 2.6472x 0.9953 2.6472 0.9953*L(2.6472) 0.9360 Beruwala y = - 0.0355 + 2.6536x 0.9651 2.6536 0.9651*L(2.6536) 0.8600 Tangalle y = + 0.3829 + 2.4637x 1.4665 2.4637 1.4665*L(2.4637) 0.9402 411 Int. J. Aquat. Biol. (2017) 5(6): 408-412 not and if the b value differs from 3, it indicates the change of the body shape as they grow. Normally allometric growth can be negative (If b<3) or positive (If b>3) (Rahman et al., 2012). The present study revealed the b value for Mount-Lavinia (2.6472), Beruwala (2.6536) and Tangalle (2.4637) were less than 3, which concludes that S. variolaris from all selected sites were close to isometric growth in weight, because “b” exponent value usually lay between 2.5 to 4.0 and that depends on the age, sex or maturity of species (Le Cren, 1951; Rahman et al., 2012). According to the above “b” value, S. variolaris have relatively negative allometric growth. The reasons for negative allometric growth should be further explored under the different environmental parameters and feeding conditions. These findings about length-weight relationship study will be helpful to get an idea about the growth of S. variolaris in Sri Lanka. Acknowledgments The authors would like to acknowledge NARA, Crow Figure 9. Length-weight relationship for Mount-lavinia population. Figure 10. Logarithmic scale Length-weight relationship for Mount-lavinia population. Figure 11. Length-weight relationship for Beruwala population. Figure 12. Logarithmic scale Length-weight relationship for Beruwala population. Figure 13. Length-weight relationship for Tangalle population. Figure 14. Logarithmic scale Length-weight relationship for Tangalle population. 412 De Zoysa et al. / Length-weight relationship of black sea urchin in Sri Lanka Island, Colombo 15, for provided grant to complete this study and we take this opportunity to thank K. Ukuwela for his invaluable comments on manuscript. References De Zoysa H.K.S., Jinadasa B.K.K.K., Edirisinghe E.M.R.K.B. (2016). Black sea urchin (Stomopneustes variolaris): nutritional composition and trace metals accumulation of edible sea urchin of Sri Lanka. Germany: LAP LAMBERT Academic Publishing. 116 p. Giese A.C., Krishnaswamy S., Vasu B.S., Lawrence J. (1964). Reproductive and biochemical studies on a sea urchin, Stomopneustes variolaris from madras harbor. Comparative Biochemistry and Physiology, 13(4): 367- 380. James D.B. (1982). Ecology of intertidal echinoderms of the Indian seas. Journal of the Marine Biological Association of India, 24(1&2): 124-129. James D.B. (1983). Research on Indian echinoderms-a review. Journal of the Marine Biological association of India, 25(1&2): 91-108. James P., Siikavuopio S. (2011). A guide to the sea urchin reproductive cycle and staging sea urchin gonad samples. Nofima, 1-20 Jayakody S. (2012). Provisional checklist of sea urchins (Echinodermata: Echinoidea) of Sri Lanka. The National Red List 2012 of Sri Lanka. 370 p. Jinadasa B.K.K.K., De Zoysa H.K.S., Jayasinghe G.D.T.M., Edirisinghe E.M.R.K.B. (2016). Determination of the biometrical parameters, biochemical composition and essential trace metals of edible sea urchin (Stomopneustes variolaris) in Sri Lanka. Cogent Food and Agriculture, 2(1): 1-12. Kroh A. (2014). Stomopneustes variolaris (Lamarck, 1816). In: A. Kroh, R. Mooi (2014). Retrieved 12-06, 2014, from World Echinoidea Database at http://www. marinespecies.org/echinoidea/aphia.php?p=taxdetails& id=212440. Le Cren E. (1951). The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). The Journal of Animal Ecology, 201-219. Rahman M., Amin S., Yusoff F.M., Arshad A., Kuppan P., Nor Shamsudin M. (2012). Length weight relationships and fecundity estimates of long-spined sea urchin, Diadema setosum, from the Pulau Pangkor, Peninsular Malaysia. Aquatic Ecosystem Health and Management, 15(3): 311-315. Reynolds J.A., Wilen J.E. (2000). The sea urchin fishery: harvesting, processing and the market. Marine Resource Economics, 15: 115-126. Salon N.A. (1985). Echinoderm fisheries of the world: a review. A Balkema, Rotterdam. pp: 109-124. Scheibling R.E., Mladenov P.V. (1987). The decline of the sea urchin, Tripneustes ventricosus, fishery of barbados: a survey of fishermen and consumers. Marine Fisheries Review, 49(3): 62-69. Smith A.B., Kroh A. (2011). The Echinoid Directory. Retrieved 12-06, 2014, from http://www.nhm.ac.uk /research-curation/projects/echinoid-directory