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Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf



A. Hosseini, P. Kochanian, J. Marammazi, V. Yavari, A. Savari and M.A. Salari-Aliabadi
 
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ABSTRACT

Length-weight relationship and spawning season of Pickhandle barracuda, Sphyraena jello (C.) were studied for one year in Boushehr waters of the Persian Gulf. In the present study, 311 specimens were collected during November 2006 to October 2007. The samples composed of 151 (48.55%) male, 160 (51.45%) female; the sex ratio was M: F = 1: 1.06. The b value ranged between 2.77 to 2.87 for male and female fishes, respectively. The relationship between body weight and length in total specimens was 2.82, indicating that this species show negative allometric growth. The peak spawning season of these fishes occur around spring, from April to June. The lowest Gonadosomatic Index recorded in August. The present study is the first record on length-weight relationship and spawning season of this species in the Persian Gulf region.

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  How to cite this article:

A. Hosseini, P. Kochanian, J. Marammazi, V. Yavari, A. Savari and M.A. Salari-Aliabadi, 2009. Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf. Pakistan Journal of Biological Sciences, 12: 296-300.

DOI: 10.3923/pjbs.2009.296.300

URL: https://scialert.net/abstract/?doi=pjbs.2009.296.300
 

INTRODUCTION

The waters of the Persian Gulf are environmentally unique with an unusual faunal assemblage (Carpenter et al., 1997). The Persian Gulf is a semi-closed water body connected to the Oman Sea through narrow Strait of Hormuz. The maximum width is 640 km with the average depth of 35 m (Reynolds, 1993). The Persian Gulf is in the subtropical zone lying almost entirely between the latitudes of 24° and 30° N and longitudes of 49° to 61° 25’ E. The entire water column is well mixed and lies within the photic zone. However, primary productivity for the Persian Gulf is apparently only in average, being higher than most the Red Sea but lower than the Arabian Sea (Sheppard et al., 1992).

The Persian Gulf possesses various commercially important fish species. Pickhandle barracuda, Sphyraena jello Cuvier, 1829 locally called Dewolmy is one of the valuable commercial fishes in the south coasts of Iran and has been classified at the top level of commercial categorization, so owing to its economic importance. Pickhandle barracudas are migratory pelagic predators that are distributed over continental shelves, estuaries and also in open oceans of tropical, subtropical and warm temperate seas (Bachok et al., 2004). The Pickhandle Barracuda (S. jello) is a long, slender schooling fish. It is silvery with variable darker bars on the body and a deeply forked, yellowish tail (Ramachandran et al., 2007). This species is of importance to fisheries in many countries and is considered a good table fish due to its excellent flesh qualities. S. jello is a commercially important pelagic fish and is caught with different types of fishing gears such as of trawls, long line and gill nets in coastal waters of Boushehr Province (Hosseini et al., 2008). Barracuda (S. jello) a trash fish of yester years is gaining importance as a potential source for product development in recent times with a landing of about 7011 ton in 2004 (MPEDA News Letter, 2006).

Length-Weight Relationship (LWR) is of great importance in fishery assessments (Garcia et al., 1989; Haimovici and Velasco, 2000). Fish length-weight relationships, which describe mathematically the correlation between fish length and weight, are useful for converting length observations into weight estimates to provide some measure of biomass (Froese, 1998). Length and weight measurements in conjunction with age data can give information on the stock composition, age at maturity, life span, mortality, growth and production (Beyer, 1987; Bolger and Connoly, 1989; King, 1996a, b; Diaz et al., 2000). Method to estimate the length-weight relationship was described by Biswas (1993) and King (2007).

There are only a limited number of studies on the LWR of this commercially important fishes worldwide and there are no studies that describe length-weight relationship and spawning season of this pelagic marine fish. Therefore, a biological investigation on S. jello in coastal waters of Boushehr Province was taken up. The aim of the present study was to determine the length-weight relationship parameters and basic information on the spawning season of S. jello from Boushehr waters (the Northeast Persian Gulf).

MATERIALS AND METHODS

The fishes used for the study were collected during November 2006 to October 2007 from the Bandargah and Jofreh harbors, two important landing centers on the Boushehr coastal. The fishing gears used in this region include gill net and trawl. At least 20-30 specimens were randomly collected per month. The randomly selected samples were transported in ice box to laboratory for further biological measurement. Identification of species was made based on Smith et al. (2003) and FAO Species identification sheets (Fischer and Bianchi, 1984). Total length (TL) was measured from the tip of the snout to the extended tip of the caudal fin. Body weight of individual fish was measured to the nearest 0.01 g with an electronic balance. Then the gonads were removed and weighed (0.001 g).

The relationship between the total length and total weight were determined by fitting the data to a potential relationship in the form of:

W = aLb

where, W is the weight in grams, L the total length in centimeters, a and b are the parameters to be estimated, with b being the coefficient of allometry (Pauly, 1984). A logarithmic transformation was used to make the relationship linear (Bagenal and Tesch, 1978):

Log w = log a+b log L

For this species a regression was used to estimate the intercept (Log a) and the regression coefficient or slope (b), using Microsoft Excel. For species with sufficient data the LWR was determined separately for each sex in addition to total fishes (311 specimens). Sex was determined by examination of the gonad tissue either with eye or with the aid of a binocular (25-40x). The overall sex ratio was assessed using Chi-square test (Zar, 1984). Statistical analyses were performed with SPSS 11.5 software package and a significance level of 0.05 was adopted. Gonadosomatic index (GSI %) = (gonad weight/total body weight)x100 was calculated for each fish and all values were averaged for each sampling date (Biswas, 1993). The gonadosomatic index or maturity index is an indirect method for estimating spawning season of a species (Biswas, 1993).

RESULTS

Based on descriptive statistics size of males ranged from 37.5 to 93.5 cm and that of females from 39.5 to 80 cm, respectively. Minimum and maximum weights of males were between 200.15 to 2850 g, respectively and that of females 235.10 and 2310.17 g, respectively. Mean values of length and weight for males and females were 58.20 ± 7.79 cm, 891.26 ± 357.87 g and 58.13 ± 7.90 cm, 867.22 ± 372.47 g, respectively. All the length data was classified into 5 cm groups and the analysis of total length distribution frequency of all individuals is shown in Fig. 1. High abundance of this species was observed in 52.5-57.5 cm length. The relationship between somatic weight and total length of the fish (Fig. 2a, b) were calculated separately for male and females. Significant differences were obtained between the b exponents and 3 for isometric growth in the sexes separately (ttest, tmale = 5.22, tfemale= 3.98, p < 0.05), indicating negative allometric nature of growth (b < 3) in the population. Moreover, there was a significant difference in the b exponent between males and females (ANCOVA, F = 8.34, p < 0.05).

Image for - Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf
Fig. 1: Length frequency distribution for S. jello from Boushehr waters (the Northeast Persian Gulf)

Table 1: Month wise sex ratio of S. jello from Boushehr waters (the Northeast Persian Gulf)
Image for - Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf

Image for - Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf
Fig. 2: Length-weight relationship curves for (a) males and (b) females of S. jello from Boushehr waters (the Northeast Persian Gulf)

Image for - Length-Weight Relationship and Spawning Season of Sphyraena jello C., from Persian Gulf
Fig. 3: Monthly mean GSI distribution of S. jello from Boushehr waters (the Northeast Persian Gulf) during Nov. 2006 to Oct. 2007.

Also determination and correlation coefficients show a high relationship between these two morphometric characteristics (p < 0.05).

The sex ratio and GSI (Gonadosomatic Index) were calculated during the study period. Table 1 shows the sex ratio observed in different months. The results of the Chi-squire test showed that there was no significant difference in sex ratio in all months except May and June. Monthly fluctuations in the GSI of both males and females are shown in Fig. 3. The highest GSI for both males and females was observed in May, which declined gradually in the following months up to August. From September onwards an increasing trend in GSI was observed in males and females indicating growth of gonads. This observation also corresponds with the gonad maturity stages. In October-November period gonads were found to be in the early maturing stage and highest numbers of fish with fully developed gonads were observed during April-May. This fish is, therefore, assumed to be a spring spawner.

As shown, the GSI for both male and female remained low ( < 1.5-2) from July to March. They increased gradually from April to May, but rapidly to reach a peak in May (testes and ovaries). The indices then decreased, falling to pre-spawning level by August. It could be stated that S. jello spawns once a year in Bousher waters during the period between April to June, with a spawning peak in May.

DISCUSSION

Due to selectivity of fishing gear, samples don’t include juveniles or very small individuals. In this context and according to Petrakis and Stergiou (1995), the use of W-L relationship should be rigorously limited to the size ranges applied in the estimation of the linear regression parameters. For this reason, it is particularly difficulty to extrapolate data to fish larvae (Pepin, 1995), juveniles (Safran, 1992) or immature stage (Bagenal, 1978).

Additionally, since samples were collected over an extended period of time, this data is not representative of a particular season or time of the years and for comparison purpose it should be considered only as mean annual values, as suggested by Petrakis and Stergionu (1995). In fact, W-L relationship isn’t constant over the whole year, varying according to factor such as food availability, feeding rate, gonad development and spawning period. However, the parameter b is characteristic of the species and generally doesn’t vary significantly through out the year, unlike the parameter a, which may vary daily, seasonally and or between different habitats (King, 1996b). The numerical value of b is nearly always between 2.5 and 3.5 and is often close to 3 (Bagenal, 1978). When b = 3, the body is increasing in all dimensions in the same proportions as it grows (Hart and Reynolds, 2002).

In a study carried out by Al-sakaff and Essen (1999) in Gulf of Eden, b value was 2.721 and 2.706 for male and female fishes of this species, respectively. The observations made in the present study (b = 2.778-2.878) also was comparable with the work of Vander-Elst (1981), where b value was estimated to be 2.81 for this species from South African waters. In a study by Abdurahiman et al. (2004) in Southern coast of Karnataka state, b values obtained for male and female fishes were 3.059 and 3.170, respectively. The difference between the results of this study and the present investigation can be attributed to difference in latitude, ecological condition and length ranges in the studied fishes in two regions. Because firstly, fishes mature earlier in tropical regions compared to temperate region and secondly, the fishes studied in India belonged to lower length range and hence had higher growth rates.

Sexual ratio had no significant differences in various months except May and June; because during spawning time, females remind in spawning area more than males (Arcand-Hoy and Benson, 1998a, b). Bachok et al. (2004) reported a sex ratio of 0.86 in Malaysian waters. Al-sakaff and Esseen (1999) reported a sex ratio of 1.187 for this fish in Gulf of Eden. The results obtained from these two studies and present investigation is in agreement. Richard et al. (1993) has stated that spawning season for this species in water of Fiji is in summer and in the regions from the coast. Related to differences in the GSI between reproductively active males and females, in reviewing the reproductive biology of the S. jello it is noted that values of males are commonly lower than those of females. Buxton (1990) pointed out that the cost of producing sperm is thought to be less than for producing eggs. The difference in male and female gondosomatic indices suggests that energy invested in gamete production by male is probably less than that invested by females.

ACKNOWLEDGMENTS

The present study was funded by the Department of Marine Biology, Research Center of Persian Gulf University and the Khorramshahr University of Marine Science and Technology (Grant No. KMSU 8234406). Authors appreciate the comments provided by the reviewers of this study and are grateful to Mr. Ahmad Falahati and Mr. Gholamhossean Eskandari.

REFERENCES

  1. Abdurahiman, K.P., T. Harishnayak, P.U. Zacharia and K.S. Mohamed, 2004. Length-weight relationship of commercially important marine fi shes and shellfi shes of the Southern Coast of Karnataka, India. NAGA WorldFish Center Quart., 27: 9-14.
    Direct Link  |  

  2. Al-Sakaff, H. and M. Esseen, 1999. Length-weight relationship of fishes from Yemen waters (Gulf of Aden and Red Sea). NAGA ICLARM, 22: 41-42.
    Direct Link  |  

  3. Bachok, Z., M.I. Mansor and R.M. Noordin, 2004. Diet composition and food habits of demersal and pelagic marine fishes from Terengganu waters, east coast of Peninsular Malaysia. NAGA World Fish Center Q., 27: 41-47.
    Direct Link  |  

  4. Bagenal, T., 1978. Methods for Assessment of Fish Production in Fresh Waters, IBP Handbook No. 3. 3rd Edn., Blackwell Scientific Publications, Oxford, pp: 101-136

  5. Beyer, J.E., 1987. On length-weight relationship. Part 1. Corresponding the mean weight of a given length class. Fishbytes, 5: 11-13.

  6. Biswas, S.P., 1993. Manual of Methods in Fish Biology. 2nd Edn., South Asian Publishers, New Delhi, pp: 157

  7. Bolger, T. and P.L. Connolly, 1989. The selection of suitable indices for the measurement and analysis of fish condition. J. Fish. Biol., 34: 171-182.
    CrossRef  |  Direct Link  |  

  8. Carpenter, E.K., F. Krupp, D.A. Jones and U. Zajonz, 1997. Living Marine Resources of Kuwait. Food and Agriculture Organization of the United Nations, Eastern Saudi Arabia, pp: 293

  9. Diaz, L.S., A. Roa, C.B. Garcia, A. Acero and G. Navas, 2000. Length-weight relationships of demersal fishes from the upper continental slope of Colombia. The ICLARM Q., 23: 23-25.
    Direct Link  |  

  10. Fischer, W. and G. Bianchi, 1984. FAO Species Identification Sheets for Fishery Purposes: Western Indian Ocean (Fishing Area 57). Food and Agriculture Organization of the United Nations, Rome, Italy

  11. Froese, R., 1998. Length-weight relationships for 18 less-studied fish species. J. Applied Ichthyol., 14: 117-118.
    CrossRef  |  

  12. Garcia, C.B., J.O. Buarte, N. Sandoval, D. Von-Schiller and P. Najavas, 1989. Length-weight relationships of demersal fishes from the Gulf of Salamanca, Colombia. Fishbyte, 21: 30-32.
    Direct Link  |  

  13. Haimovici, M. and G. Velasco, 2000. Length-weight relationship of marine fishes from Southern Brazil. The ICLARM Q., 23: 14-16.

  14. Hart, J.B. and D. Reynolds, 2002. Hand Book of Fish Biology and Fisheries. 3rd Edn., Blackwell Publishing, USA., pp: 107

  15. King, M., 1995. Fisheries Biology: Assessment and Management. 2nd Edn., Blackwell Publishing, UK., pp: 341

  16. King, R.P., 1996. Length-weight relationships of Nigeria Freshwater fishes. Naga ICLARIM Q., 19: 49-52.
    Direct Link  |  

  17. King, R.P., 1996. Length-weight relationship of Nigerian Coastal water fishes. NAGA: ICLARM Q., 19: 53-58.
    Direct Link  |  

  18. MPEDA News Letter, 2006. Statistics of marine products exports-2004. India: The Marine Products Export Development Authority.

  19. Pepin, P., 1995. An analysis of the length-weight relationship of larval fish: Limitations of the general allometric model. Fish. Bull., 93: 419-426.
    Direct Link  |  

  20. Petrakis, G. and K.I. Stergiou, 1995. Weight-length relationships for 33 fish species in Greek waters. Fish. Res., 21: 465-469.
    CrossRef  |  

  21. Reynolds, R.M., 1993. Physical oceanography of the Gulf Strait of Hormuz and the Gulf of Oman-Results from the Mt. mitchell expedition. Marine Pollut. Bull., 27: 35-59.
    CrossRef  |  

  22. Richards, A., M. Lagibalavu, S. Sharma and K. Swamy, 1993. Fiji fisheries resources profiles. Forum Fisheries Agency, Fiji Fisheries and Forestry, Ministry of Agriculture, pp: 231.

  23. Safran, P., 1992. Theoretical analysis of the weight-length relationship in fish juveniles. Mar. Biol., 112: 545-551.
    CrossRef  |  

  24. Sheppard, C., A. Price and C. Roberts, 1992. Marine Ecology of the Arabian Region: Patterns and Processes in Extreme Tropical Environments. 2nd Edn., Academic Press, New York, USA., Pages: 359

  25. Smith, J.L.B., M. Smith and P. Heemstra, 2003. Smiths'Sea Fishes. 3rd Edn., Struik Publishers, Springer Verlag, Berlin, London, Paris

  26. Vander-Elst, R., 1981. A Guide to the Common Sea Fishes of Southern Africa. 2nd Edn., C. Struck, Cape Town, pp: 367

  27. Arcand-Hoy, L. and Benson, W.H., 1998. Fish reproduction: An ecologically relevant indicator of endocrine disruption. Environ. Toxicol. Chem., 17: 49-57.
    CrossRef  |  

  28. Buxton, C.D., 1990. The reproductive biology of Chrysoblephus laticeps and C. cristiceps (Teleostei: Sparidae). J. Zool., 220: 497-511.
    Direct Link  |  

  29. Hosseini, S.A., S.H. Jamili, T. Valinassab, G.H. Vosoghi and M.R. Fatemi, 2008. The study on feeding and spawning behavior of Sphyraena jello (Pickhandle baracuda) in the Persian Gulf. World Aquaculture 2008, May 19-23, 2008, Busan, Korea, pp: 246.

  30. Pauly, D., 1984. Fish Population Dynamics in Tropical Waters: A Manual for Use with Programmable Calculators. 1st Edn., International Center for Living Aquatic Resources Management, Manila, Philippines, ISBN-13: 9789711022037
    Direct Link  |  

  31. Ramachandran, D., M. Mohan and T.V. Sankar, 2006. Physicochemical characteristics of muscle proteins from barracuda (Sphyraena jello) of different weight groups. LWT Food Sci. Techn., 40: 1418-1426.
    CrossRef  |  

  32. Zar, J.H., 1984. Biostatistical Analysis. 4th Edn., Prentice Hall, Englewoods Cliffs, New Jersey.

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