Abstract
The age structure, growth, mortality, and exploitation status of the Chrysochir aurea stock in West Bengal coast, India, were assessed. A sample of 618 specimens with total lengths ranging from 124 to 417 mm were collected from commercial trawlers between September 2021 and September 2022. The length-frequency distribution was analysed using the FiSAT II tool. The growth parameters asymptotic length (L∞), catabolic coefficient (K), and initial condition factor (t0) were determined to be 435.23 mm, 0.26 yr-1, and -0.309 years, respectively. The total (Z), natural (M), and fishing (F) mortality rates were estimated at 1.09, 0.35, and 0.74 yr-1, respectively. A consistent recruitment trend was seen throughout the year, with two peaks, one from February to May and the other from July to November, with a length at first capture (LC) of 177.95 mm. The current exploitation level (Enow) and maximum exploitation level (Emax) were calculated at 0.68 and 0.60 indicating overexploitation of the stock along the coast. The yield was projected to be 160.826 t at the current fishing level (f = 1.0) and 164.866 t at the maximum fishing level (f = 0.9). To create a sustainable fishery in the future, a reduction in fishing effort is suggested.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Introduction
The Indian, Pacific, and Atlantic Oceans are home to a diverse population of sciaenids, also commonly referred to as drummers or croakers belonging to the family Sciaenidae. They are one of India's most valuable demersal fisheries resources, accounting for around 3.3% of all marine fish landings in the entire country. Their share of the West Bengal state's total marine fish and demersal fish landings, which has 158 km of coastline, is around 7.21% and 23.44%, respectively (CMFRI 2022).
The optimal strategy for exploiting and maintaining aquatic living resources can be determined with the use of population age structure (Sparre and Venema 1998). It makes quantitative forecasts on how alternative management strategies will affect fish populations using a variety of statistical and mathematical models. The computation of growth, mortality, and recruitment patterns is imperative to comprehend population dynamics rates and is made possible by research on population dynamics in fishes (Chung and Woo 1999; Bhakta et al. 2020). Age at first maturity, spawning frequency, individual and stock reactions to environmental changes, recruiting success, stock structure, etc. are just a few of the issues that these factors can help us better understand (Johnson et al. 2020; Bhakta et al. 2022). The length-frequency distribution is an essential biometric statistic for assessing the dynamic rates of recruitment, growth, mortality, yields, and stock biomass in a particular ecosystem (Sabbir et al. 2021). One of the main objectives of fish stock assessments is to offer knowledge on the most effective uses of resource management. Several models must be used to assess how diverse environmental changes affect the biological and physical traits of a fish species, family, or group (Sarkar et al. 2018).
Reeve’s croaker, Chrysochir aurea (Richardson 1846), is one of the most commercially significant species that is widely distributed in the Indo-West Pacific; it is primarily found in Sri Lanka, through the Bay of Bengal, to southern China (including Taiwan), the southern part of Indonesia, and Malaysia (Sasaki 2001; Jalal et al. 2012). It lives mostly in brackish and marine coastal areas. Effective fishery management and the development of sustainable fisheries require an assessment of population structure, including age and growth, as well as an assessment of a fish stock (Hilborn and Walters 1992; Campana 2001; Bhuyan et al. 2012). In general, and especially off the coast of West Bengal, India where the resource significantly contributes to trawl landings, information about the population parameters and stock assessment of C. aurea is noticeably lacking. As a result, the present research was undertaken to estimate population parameters and evaluate the stock status of C. aurea along the said coast.
Materials and Methods
Study Area
The coastline of West Bengal with a continental shelf area of 17,049 sq. km spread in two districts namely South 24-Parganas and Purba Medinipur. Purba Medinipur has an open coast on the south-eastern part of West Bengal. The study area was selected purposively in the inshore areas of the Bay of Bengal along the coast of Digha (Latitude 21.6800° N and Longitude 87.5500° E), Purba Medinipur
Sampling and Data Collection
Length frequency data were collected monthly at the Digha fish landing center from September 2021 to September 2022. The specimens were caught using a trawl net with a mesh size of between 18 and 35 mm at a depth of between 10 and 69 m and brought to the laboratory for further study in an insulated box that was kept frozen. Using a standard measuring board, the total length (TL) of the fish specimens was measured from the tip of the anterior-most region of the body to the tip of the caudal fin to the nearest mm accuracy. Total weight was measured to the nearest mg using digital electronic balance. The collected length frequency data were grouped into 10 mm class intervals, and monthly length frequency data were fed into FAO-ICLARM Stock Assessment Tool (FiSAT II) software version 1.2.2 (Gayanilo et al. 2005) to estimate various population parameters and yields and to assess stock.
Estimation of Population Parameters
The length-weight relationship was computed statistically by expressing the parabolic equation W = aLb. This equation was expressed logarithmically as Log W = log a + b log L (Le Cren 1951). Where W = weight of fish in g and L = length of fish in mm, ‘a’ and ‘b’ are intercept and regression coefficients, respectively.
Growth parameters like asymptotic length (L∞) and growth coefficient (K) were estimated using the Electronic Length Frequency Analysis (ELEFAN I) module in FiSAT II, and the initial condition factor or age at zero-length (t0) was calculated from Pauly’s (1979) empirical equation as
where L∞ is the asymptotic length, K is the growth coefficient, and t0 is the initial condition factor or age at zero length.
The growth and age were estimated by employing the Von Bertalanffy (1938) growth equation
where Lt is the length of the fish at age t, e is exponential, L∞ is the asymptotic length, K is the growth coefficient, and t0 is the age at zero length. The growth performance index (φ') for C. aurea was estimated as per Pauly and Munro (1984)
where L∞ is the asymptotic length, K is the growth coefficient
The total mortality (Z) was calculated from the length-converted catch curve method (Pauly 1983a, 1984a) by using FiSAT II and the natural mortality (M) was estimated by Pauly’s (1980) empirical formula
where ‘T’ is the mean annual water temperature, which was taken as 27°C (India Meteorological Department, Kolkata). Fishing mortality (F) was estimated by subtracting natural mortality (M) from total mortality (Z), i.e., F = Z - M.
The exploitation level (E) was estimated by using the following equation
Stock Assessment
For stock assessment studies, the probability of capture was obtained from length-converted catch curves by backward extrapolation of the catch curve. Long-structured virtual population analysis was done by Pauly (1984b). The relative yield per recruit (Y’/R) and biomass per recruit (B’/R) at different levels of F were estimated from Beverton and Holt’s (1966) relative yield per recruit model. The status of the stock was evaluated based on Y’/R. The longevity (tmax) of the species was estimated by the equation given by Pauly (1983b) as:
where ‘tmax’ is the longevity of the species.
Results
Length-Frequency Distribution
Analysis of catch composition data for C. aurea from the West Bengal coast revealed that the species is existing during the year along the coast. Month-wise length-frequency data are presented in Fig. 1. The size of C. aurea ranged from 124 to 417 mm with an average length of 221.07±44.56 mm in total length. According to the percentage length frequency data, the length groups of 200–209 mm (10.19%), followed by 190–199 mm (9.55%) represented the majority of the species' commercial catches (Fig. 2).
Population Parameters
Age and Growth
The estimated growth parameters L∞, K and t0 were determined as 435.23 mm, 0.26 yr-1, and -0.309 years, respectively. Von Bertalanffy’s growth equation was subsequently obtained as: Lt = 435.23[1-e-0.26(t+0.309)]. Accordingly, lengths attained by C. aurea were estimated as 125, 198, 251, 293 and 325 mm at the end of 1, 2, 3, 4, and 5 years, respectively, by employing the growth equation (Fig. 3). The smallest length recorded was 124 mm, corresponding to an age of 0.98 years. Growth performance index (φ') and the maximum life span (tmax) of C. aurea were estimated as 4.69 and 11.23 years, respectively. The pooled linear relationship between length and weight of C. aurea was obtained as Log W = −5.6407 + 3.2756 Log L with R2 value of 0.9855.
Mortality Parameters
The estimated total mortality (Z) was 1.09 yr-1 (Fig. 4), and the values of natural mortality (M) and fishing mortality (F) were 0.35 yr-1 at 27°C annual mean temperature and 0.74 yr-1, respectively. The current exploitation level (Enow) was estimated at 0.68.
Stock Assessment
Recruitment Pattern
Using the estimated values of growth parameters, the recruitment pattern was analysed from recruitment curves. The length frequency data of C. aurea indicated a persistent recruitment pattern during the year (Fig. 5), with two peaks, one during the months of February to May and another during July to November. The midpoint, 124.5 mm of the smallest length group (120- 129 mm) in the catch was taken as length at recruitment (Lr) for C. aurea.
Probability of Capture (LC)
The monthly length-frequency data was pooled together, and the frequency, cumulative frequency, and cumulative percentage were calculated by applying the length-converted catch curve method. The value of LC or L50% (the length at which 50% of fish become vulnerable to the gear) was estimated at 177.95 mm from the graph (Fig. 6), and the corresponding age was 1.71 years.
The input parameters used for virtual population analysis (VPA) were L∞ of 435.23 mm, K of 0.26 yr-1, M of 0.35 yr-1, ‘a’ of 0.0000023 and ‘b’ of 3.2756 from the length-weight relationship. The results obtained from length structured VPA depicted that C. aurea along the West Bengal coast is overexploited.
The exploitation ratio was estimated at 0.68 (Fig. 7). The fishing mortality was found to be outweighed by the length groups of 200–209 mm (Fig. 7), reaching the highest value of 1.4783 yr-1 at the 270–279 mm length group, followed by 1.0919 yr-1 at the 260–269 mm length group. The shorter group showed relatively low fishing mortalities. The length groups of 120–129 mm to 140–149 mm were subjected to mortality mainly. The highest number of fish populations (2285288) be noticed in the 120–129 mm length group, with a biomass of 46.5 tonnes and a respective fishing mortality of 0.0132 yr-1. The largest length group of 410–419 mm showed the least number of fish population (2338) with fishing mortality of 0.74 yr-1 and a respective biomass of 18.5 t. The biomass increased from 46.5 metric tonnes to the highest of 163.46 tonnes from the length class of 120–129 mm to 220–229 mm and then gradually decreased to its lowest level of 18.5 tonnes at the 410–419 mm length class.
Yield and Yield Per Recruit
The Beverton and Holt relative yield per recruit (Y’/R) and relative biomass per recruit (B’/R) were estimated from the knife-edge selection of the size at first capture, which was 177.95 mm. The input data were LC/L∞ (0.41) and M/K (1.35). The Emax, E0.1 and E0.5 values were obtained as 0.60, 0.521, and 0.337, respectively, from the knife-edge selection method (Fig. 8).
Thompson and Bell Prediction Model
The length based VPA file was stored and further used as input along with the price assigned according to each length group for the analysis of Thompson and Bell’s (1934) prediction model (Fig. 9). The output shows an array of ‘f-factors with corresponding yield, biomass, and values. The ‘f-factor’ of 1.0 indicates the present level of fishing. The result of the Thompson and Bell prediction model indicated that yield increased from 73.76 tonnes at an f-factor of 0.2 to a maximum sustainable yield (MSY) of 164.866 t at an f-factor of 0.9. Beyond the fishing pressure (‘f-factor’ = 0.9), yield has declined. The maximum value of the catch was obtained at the ‘f-factor of 0.7.
Discussion
Age and Growth
Understanding the composition of the fish population, the impact of a particular brood or age group on catch fluctuations, and the length or age at capture and maturity are all highly important aspects of fishery management. The east coast of India has fewer studies on sciaenid growth parameters and stock evaluation than the west coast. Since work on C. aurea population parameters and stock assessment has not yet been done, earlier findings on other closely related sciaenid species have been used to compare the findings of the present study (Table 1).
Chakraborty et al. (2000) and Santhoshkumar et al. (2017) reported L∞ as 469 mm and 372.8 mm, K as 0.47 yr-1 and 0.27 yr-1, φ' as 3.01 and 2.57, respectively, of Otolithes ruber from Tamil Nadu, southeast coast of India where values differed for the species from the same study area. Otolithoides pama from the Hooghly-Matlah estuary in West Bengal, northeast coast of India reported values for L∞ and K as 418 mm and 0.58 yr-1 (Bhakta et al. 2020). O. ruber has been studied all over the world since it appears to have a more widespread distribution. According to various sources (Morgan 1984; Ingles and Pauly 1984; Gislason 1985; Schultz 1992; Almatar 1993; Chakraborty et al. 2000; Brash and Fennessy 2005; Bhuyan et al. 2012), the L∞ of this species varied between 295 and 696 mm, and its K value ranged between 0.14 and 0.67 yr-1. For the several sciaenids from the Indian seas, the value of K ranged between 0.21 to 2.0 (Table 1).
In the present investigation, the asymptotic length of C. aurea is slightly on the higher side, and the K value (0.26 yr-1), appears low compared to other sciaenids reported by previous authors. Such low K values in the range of 0.14-0.26 yr-1 for O. biauritus from Mumbai (Jayaprakash 1976; Manojkumar et al. 1992) and 0.28 yr-1 for Pseudotolithus elongatus from Nigeria (Nawa 1987) have been recorded. It is evident that there is an inverse relationship between L∞ and K (Chakraborty 1987, 2006). The largest fish of 417 mm recorded in the present study and low K value justifies a higher L∞ value (435.23 mm) for this species.
The overall growth performance of the fish population as measured by growth in length is represented by the growth performance index (φ') (Pauly and Munro 1984). The range of φ' for sciaenid species found on the east coast varied between 2.57 and 3.36 (Table 1). Though the phi-prime value in the present study (4.69) slightly deviated from the earlier observations, which ranged from 6.13 to 6.87. For sciaenid species found in Bombay waters (northwest coast), such as Johnius macrorhynus, Johnius vogleri, Johnius sina, Johnius dussumieri, Otolithes cuvieri and Pennahia macrophthalmus, these values were comparatively higher (Chakraborty 1997, 2001). The main causes of these fluctuations include changes in K values, environmental factors and varying fishing intensities. Growth factors vary from stock to stock and sex to sex within the same species, also due to differential growth rates of successive cohorts owing to environmental conditions (Chakraborty 1996; Sparre and Venema 1998).
Mortality Parameters
No reports of mortality parameters for C. aurea are available from India or elsewhere. The Z and F of sciaenids recorded by the earlier investigators from the east coast of India ranged between 2.45 yr-1 and 6.18 yr-1 and, 0.97 yr-1 and 4.07 yr-1, respectively (Table 1). The present study indicated that the F is almost double the M which clearly implies the excess fishing pressure on C. aurea along the West Bengal coast. The earlier studies (Table 1) on different sciaenid species from Indian waters also reported higher fishing mortality than natural mortality (Murty 1986; Chakraborty 1987; Manojkumar et al. 1992; Chakraborty et al. 2000; Chakraborty 2006; Mandal and Nagesh 2007; Bhakta et al. 2020). According to Chakraborty (1994), fast-growing fish with a high K value would have a high M and vice versa, and fish with a high L∞ would have a low M. In the current study, C. aurea had relatively higher L∞, K and lower M values, which are justified.
The mortality rate of C. aurea in the present study associated with fishing mortality is on the higher side, and around 60% of the catch (Figure 2) was below the length at first maturity (Lm) reported by Jana (2023) (218 mm for males and 222 mm for females) and Ni (2018) (263 for males and 210 mm for females) which may be due to the use of small cod-end mesh sizes of 18 to 35 mm. Hence, there is a great need for mesh size regulations to avoid overfishing. The age of the species and the predator abundance present in the surroundings, among other environmental factors, have a significant impact on the natural mortality coefficient in fish. (Pauly 1980, 1983a; Jones 1984).
Ratio of Mortality and Growth Coefficient
The M/K value shows how the natural mortality coefficient and physiological variables interact. The growth coefficient, K is related to fish longevity, and the M/K values ranging from 1.5 to 2.5 or lower appear to be most common (Beverton and Holt 1959; Prince et al. 2015). Sparre and Venema (1998) suggested that natural mortality could be associated with environmental temperature because higher temperatures result in a high metabolic rate. If M/K<0.5, growth is high relative to mortality; if M/K>2.0, natural mortality exceeds growth, indicating that many fish will die before reaching their optimum level of growth. According to Chakraborty (2001), six species of Indian sciaenids had M/K values that ranged from 1.81 to 2.18. The M/K value in the current investigation was assessed to be 1.35, although slightly lower than the values specified by Chakraborty (2001), the M estimated in the current study is found to be realistic.
The ratio of Z/K is typically believed to be dominated by growth when it is less than 1, dominated by mortality when it is equal to 1 and indicates a high level of exploitation when equal to or more than 2 (Chakraborty 2006). The Z/K value was estimated to be 4.15 in the present study on C. aurea, indicating a very high level of exploitation. Chakraborty (2006) also found a high level of exploitation (Z/K = 3.48) for O. biauritus from the northwest coast of India.
Exploitation Level
The degree of exploitation (Enow) indicates whether a stock is overfished, underfished, or being fished to its maximum potential. The current study's exploitation level was calculated to be 0.68, which is significantly higher than the ideal level of 0.5 suggested by Gulland (1983). The West Bengal coast's C. aurea stock is overexploited as evidenced by the maximum exploitation level (Emax) of 0.60, which is lower than the current level of exploitation (Enow = 0.68). Additionally, studies reported by several experts revealed E values of greater than 0.5 for many sciaenid species near the Indian coast (Table 1). To avoid stock depletion and promote sustainable sciaenid fisheries throughout the Indian coast, all these authors, including the present one, recommended reducing fishing effort in addition to the monsoon fishing ban and mesh size regulations which are already in vogue.
Stock Assessment
Recruitment Pattern
The recruitment pattern of C. aurea in the current study showed a continuous recruitment pattern with two peaks, one during the months of February–May and another during the months of July–November. The availability of juveniles throughout the year also lends credence to it. Several researchers have noted a continuous recruitment trend throughout the year in Indian seas with changing peaks in several sciaenid species (Chakraborty et al. 2000; Manojkumar 2007; Santhoshkumar et al. 2017; Sabbir et al. 2021). The current study's findings of a prolonged spawning season suggest mixing of subpopulations that spawn at varying times depending on the various fishing locations (Muktha et al. 2015). The study on reproductive biology from Southwestern Taiwan found that C. aurea is a multiple spawner and primarily spawns from July to December, which lends confirmation to the current finding (Ni 2018).
Probability of Capture
In the current study, the length at first capture (LC) was assessed to be 177.95 mm, which is less than the length at maturity of the species reported by Ni (2018) and Jana (2023) indicating that they were caught before they reached maturity and began to reproduce, sign of growth overfishing. This may be prevented by increasing the size of the fish when they are harvested through regulation of mesh size.
Length Structured Virtual Population Analysis
The virtual population analysis of the C. aurea population from the West Bengal coast demonstrated that the highest fishing mortality of 1.4783 at the length group of 270–279 mm, followed by 1.0919 at 260–269 mm, which was consistent with the observation of Rao et al. (1992). A similar finding was achieved in O. cuvieri from northwest coast of India by Telvekar (2006), who found higher fishing mortality rates in medium-length groups owing to the underrepresentation of the smaller and larger-length fish groups in commercial catches.
Yield on Prediction Model
Thompson and Bell's prediction model indicated that the yield at the present fishing level (‘f-factor = 1) was 160.826 t (Fig. 9). The maximum yield of 164.866 t could be obtained at a fishing level of 0.9. The present study indicated that the yield of C. aurea from the West Bengal coast is already in a declining stage at the present fishing effort (‘f-factor = 1). So, a further increase in fishing effort will decrease the yield and drastically reduce the biomass. Therefore, a reduction of fishing effort to 0.9 is suggested for the sustainable fishery of C. aurea along the coast. The estimated exploitation value (0.68) obtained from the present study is higher than that of the Emax value (0.60) indicated the species is already experiencing high fishing pressure, which is in accordance with the results reported for several species of sciaenids in Indian waters (Chakraborty et al. 2000; Rahangdale et al. 2022; Abinaya and Sajeevan 2023).
Conclusion
The present study suggested a combination of reduction of fishing efforts and mesh size regulation to ensure sustainable benefits from sciaenid resources along the coast of West Bengal.
Data Availability
No datasets were generated or analysed during the current study.
The data that support the findings of this study are not openly available due to reasons of sensitivity and are available from the corresponding author upon reasonable request.
References
Abinaya R, Sajeevan M (2023) Stock assessment of sin croaker Johnius dussumieri (Cuvier, 1830) fishery by different production model approach from Tamil Nadu, Southeast Coast of India. Turk J Fish Aquat Sci 23(5):TRJFAS22465. https://doi.org/10.4194/TRJFAS22465
Almatar S (1993) A comparison of length- related and age-related growth parameters of newaiby, Otolithes ruber in Kuwait waters. Naga ICLARM Q 16(1):32–34
Beverton RJH, Holt SJ (1959) A review of the lifespans and mortality rates of fish in nature, and their relation to growth and other physiological characteristics. Ciba foundation symposium-the lifespan of animals (colloquia on ageing), 5th edn. John Wiley & Sons Ltd, Chichester, pp 142–180
Beverton RJH, Holt SJ (1966) Manual of methods for fish stock assessment. part 2. tables of yield function. FAO Fish Biol Tech Paper 1(38):67
Bhakta D, Das SK, Das BK, Nagesh TS, Samanta R (2020) Growth, mortality and exploitation status of Otolithoides pama (hamilton, 1822) from hooghly-matlah estuary of West Bengal, India. Reg Stud Mar Sci 39:101451. https://doi.org/10.1016/j.rsma.2020.101451
Bhakta D, Das SK, Das BK, Nagesh TS, Behera BK (2022) Fishery and population dynamics of Otolithoides pama (hamilton, 1822) from hooghly-matlah estuary of West Bengal, India. Aquat Ecosyst Health 25(2):36–43. https://doi.org/10.14321/aehm.025.02.36
Bhuyan SK, Jena JK, Pillai BR, Kumar P, Chakraborty SK (2012) Studies on the growth of Otolithes ruber (Bloch & Schneider, 1801), Johnius carutta Bloch, 1793 and Pennahia macrophthalmus (bleeker, 1850) from paradeep coast, Orissa, India. Indian J Fish 59(2):89–93
Brash JM, Fennessy ST (2005) A preliminary investigation of age and growth of Otolithes ruber from KwaZulu-Natal, South Africa, west indian. Ocean J Mar Sci 4(1):21–28. https://doi.org/10.4314/wiojms.v4i1.28470
Campana SE (2001) Accuracy, precision and quality control in age determination, including a review of the use and abuse of age validation methods. J Fish Biol 59(2):197–242. https://doi.org/10.1111/j.1095-8649.2001.tb00127.x
Chakraborty SK (1994) Population dynamics of sciaenid Johnius macrorhynus (Pisces/Perciformes /Sciaenidae) from Bombay waters. Indian J Geo-Mar Sci 23(2):86–89
Chakraborty SK (1996) Stock assessment of big eye croaker Pennahia macrophthalamus (Bleeker) (Pisces/Perciformes/Sciaenidae) from Bombay waters. Indian J Mar Sci 25:316–319
Chakraborty SK (1997) Growth, mortality and yield per recruit of bearded croaker Johnius dussumieri (Val.) from Mumbai waters. Indian J Fish 44(1):45–49
Chakraborty SK (2001) Growth studies of sciaenids from Mumbai waters using the Bhattacharya’s method. NAGA, ICLARM Q 24(1–2):40–41
Chakraborty SK (2006) Growth and mortality of bronze croaker, Otolithoides biauritus (Cantor) from Mumbai waters. Indian J Fish 53(1):85–89
Chakraborty SK, Devadoss P, Manojkumar PP et al (2000) The fishery, biology and stock assessment of jew fish resources of India. Marine Fisheries Research and Management. CMFRI, Kochi, pp 604–616
Chakraborty SK (1987) Population dynamics of Otolithes cuvieri (Trewavas) off Bombay waters. In: James PSBR (ed) CMFRI Bulletin National Symposium on Research and Development in Marine Fisheries Sessions I & II, CMFRI, Cochin, India, 44(1):238–244
Chung KC, Woo NYS (1999) Age and growth by scale analysis of Pomacanthus imperator (Teleostei: Pomacanthidae) from Dongsha Islands, Southern China. Environ Biol Fish 55:399–412. https://doi.org/10.1023/A:1007571532648
CMFRI (2022) Annual Report 2021–2022. Central Marine Fisheries Research Institute, Kochi, p 300
Gayanilo FC Jr, Sparre P, Pauly D (2005) FAO – ICLARM Stock Assessment Tools II (FiSAT II): Revised Version. User’s Guide. FAO Computerized information series (Fisheries), Rome, FAO
Gislason H (1985) A short note on the available information about demersal fish on the shallow part of the Sofala Bank. Rev Invest Pesq 13:83–95
Gulland JA (1983) Fish Stock Assessment: A Manual of Basic Method. FAO/Wiley Series on Food and Agriculture, Rome
Hilborn R, Walters CI (1992) Quantitative fisheries stock assessment; choice, dynamics and uncertainty, 1st ed. Chapman and Hall, New York: International Thomson Publishing, (p 570)
Ingles J, Pauly D (1984) An atlas of the growth, mortality and recruitment of Philippine fishes. ICLARM Tech Rep 13:127
Jalal KC, Kamaruzzaman BY, Arshad A, Ara R, Rahman MF (2012) Diversity and distribution of fishes in tropical estuary Kuantan, Pahang, Malaysia. Pak J Biol Sci 15(12):576–582. https://doi.org/10.3923/pjbs.2012.576.582
Jana S (2023) Spatio-temporal distribution and stock assessment of Chrysochir aurea (Richardson, 1846) along the coast of West Bengal. Dissertation, West Bengal University of Animal and Fishery Sciences
Jayaprakash AA (1976) Age and growth of the juveniles of Koth Otolithoides brunneus (Day) in Bombay waters. Indian J Fish 23(1&2):86–96
Jayasankar P (1995) Population dynamics of big-eye croaker Pennahia macrophthalmus and blotched croaker Nibea maculata (Pisces/Perciformes/Sciaenidae) in the trawling grounds off Rameswaram island, east coast of India. Indian J Mar Sci 24(3):153–157. http://nopr.niscpr.res.in/handle/123456789/37320
Johnson C, Sarkar UK, Koushlesh SK, Das AK, Das BK, Naskar BK (2020) Population structure of Nile tilapia and its impact on fisheries of a tropical impacted reservoir, Central India. Environ Sci Poll Res 27:29091–29099. https://doi.org/10.1007/s11356-020-09234-w
Jones R (1984) Assessing the effects of changes in exploitation pattern using length composition data (with notes on VPA and cohort analysis). FAO Fish Tech Paper 256:118
Le Cren ED (1951) The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). J Ani Ecol 20:201–219. https://doi.org/10.2307/1540
Mandal B, Nagesh TS (2007) Growth, mortality and exploitation level of Gangetic bola, Johnius gangeticus Talwar from estuarine region of Kakdwip, West Bengal, India. Environ Ecol 25(4):1012
Manojkumar PP (2007) Fishery of sciaenids off Veraval with special reference to growth, mortality and stock assessment of Otolithes cuvieri (Trewavas, 1974). Indian J Fish 54(1):21–26
Manojkumar PP, Acharya P, Gulati D (1992) Population dynamics and stock assessment, of koth (Otolithoides biauritus, Cantor, 1850) along the North-West coast of India. J Indian Fish Assoc 22:33–40
Morgan GR (1984) Application of length based stock assessment to Kuwait fish stocks. ICLARM News Lett 6(4):3–4
Muktha M, Maheswarudu G, Rohit P, Laxmilatha P, Das M, Rao KN (2015) Biology and stock assessment of the bigeye croaker Pennahia anea (Bloch, 1793) landed along Andhra Pradesh, north-east coast of India. Indian J Fish 62(1):46–51
Murty VS (1985) Multispecies stock assessment with particular reference to major demersal fish species in the trawling grounds off Kakinada. J Mar Biol Assoc India 27(1&2):39–48
Murty VS (1986) Growth and yield per recruit of Johnius (Johnius) carutta Bloch in the trawling grounds off Kakinada. Indian J Fish 33(2):163–170
Nawa IG (1987) A study on growth of Pseudotolithus elongatus, Chrysichythys nigrodigitatus and Cynoglossus goreensis occurring in the cross river estuary. In : Proceedings of the 4th Annual Conference of the Fisheries Society of Nigeria (FISON). Lagos, Nigeria, pp 162–172
Ni HY (2018) Reproductive biology of Chrysochir aureus and Otolithes ruber in the waters off southwestern Taiwan. Dissertation, National Kaohsiung Sun Yat-sen University
Pauly D (1980) On the interrelationships between natural mortality, growth parameters, and mean environmental temperature in 175 fish stocks. ICES J Mar Sci 39(2):175–192
Pauly D (1983a) Length converted catch curves: a powerful tool for fisheries research in the tropics (Part-1). ICLARM, Fish Byte 1(2):9–13
Pauly D (1983b) Some simple methods for the assessment of tropical fish stocks. FAO Fish Tech Pap 234:52
Pauly D (1984a) Length-converted catch curves: a powerful tool for fisheries research in the tropics (Part II). ICLARM, Fish Byte 2(1):17–19
Pauly D (1984b) Fish population dynamics in tropical waters: a manual for use with programmable calculators. ICLARM Stud Rev 8:325
Pauly D, Munro JL (1984) Once more on the comparison of growth in fish and invertebrates. Fish Byte 2(1):1–21
Pauly D (1979) Theory and management of tropical multispecies stocks: a review, with emphasis on the Southeast Asian demersal fisheries. ICLARM Stud Rev 1:1–35
Prince JD, Hordyk AR, Valencia SR, Loneragan NR, Sainsbury KJ (2015) Revisiting the concept of Beverton-Holt life-history invariants with the aim of informing data-poor fisheries assessment. ICES J Mar Sci 72:194–203. https://doi.org/10.1093/icesjms/fsu011
Rahangdale S, Zacharia PU, Kumar R, Vase V (2022) Evaluating the stock status of 10 croaker species landed along the north-eastern Arabian Sea using the length-based Bayesian biomass approach. Front Mar Sci 9:952795. https://doi.org/10.3389/fmars.2022.952795
Rajkumar U, Rao KN, Kingsly HJ (2004) Sciaenid fishery off Visakhapatnam with some aspects of population dynamics of Johnius carutta (Bloch). Indian J Fish 51(3):311–318
Rao TA, Lal Mohan RS, Chakraborty SK, Murty VS, Nair KV, Vivekanandan E, Raje SG (1992) Stock assessment of sciaenid resources of India. Indian J Fish 39(1&2):85–103
Richardson J (1846) Report on the ichthyology of the seas of China and Japan. Report of the British Association for the Advancement of Science 15th meeting 1845:187–320
Sabbir W, Rahman MA, Hossain MY, Hasan MR, Mawa Z, Rahman O, Tanjin S, Sarmin MS (2021) Stock assessment of hooghly croaker Panna heterolepis in the bay of Bengal (southern Bangladesh): implications for sustainable management. Heliyon 7(8):e07711. https://doi.org/10.1016/j.heliyon.2021.e07711
Santhoshkumar S, Jawahar P, Rajagopalsamy CBT, Venkatasamy M (2011) Growth and mortality characteristics of Nibea meculata (Bloch & Schneider, 1801) exploited off Thoothukudi coast, Tamil Nadu. Indian J Fish 58(4):17–20
Santhoshkumar S, Rajagopalsamy CBT, Jawahar P, Jayakumar N, Pavinkumar P (2017) Growth and mortality characteristics of Otolithes ruber (Schneider, 1801) exploited off Thoothukudi coast, Tamil Nadu. J Entomol Zool Stud 5(4):1746–1749
Sarkar UK, Naskar M, Roy K, Sudheesan D, Gupta S, Bose AK, Srivastava PK, Nandy SK, Verma VK, Sarkar SD, Karnatak G (2018) Baseline information of reproduction parameters of an amphidromous croaker Johnius coitor (Hamilton, 1822) from Ganga river basin, India with special reference to potential influence of climatic variability. Aquat Living Res 31:4. https://doi.org/10.1051/alr/201704
Sasaki K (2001) Sciaenidae. In: Carpenter KE and Niem VH (eds) FAO Species Identification Guide for Fishery Purposes. The Living Marine Resources of the Western Central Pacific. Volume 5: Bony Fishes Part 3 (Menidae to Pomacentridae). Rome, FAO, pp 3117–3174
Schultz N (1992) Preliminary investigations on the population dynamics of Otolithes ruber (Sciaenidae) on Sofala Bank, Mozambique. Rev Invest Pesq 21:41–49
Sparre PJ, Venema SC (1998) Introduction to tropical fish stock assessment Part I: Manual FAO Technical Paper No 306/ Rev 2. Rome, FAO
Telvekar PA (2006) Biology and Stock assessment of Johnieops sina (Cuvier 1830) from Mumbai waters. Dissertation, Central Institute of Fisheries Education
Thompson WF, Bell FH (1934) Biological statistics of the Pacific halibut fishery. 2. Effects of changes in intensity upon total yield and yield per unit of gear. Report of the International Fisheries (Pacific halibut) Commission
Vivekanandan E (1985) The sciaenid fishery and some biological aspects of Johnius carutta from Madras. J Mar Biol Assoc India 27(1&2):9–14
Von Bertalanffy L (1938) A quantitative theory of organic growth (inquiries on growth laws. II). Human Biol 10(2):181–213
Acknowledgments
The vice chancellor of West Bengal University of Animal and Fishery Sciences in Kolkata is acknowledged by the authors for providing the facilities and infrastructure needed to complete the work. Throughout the duration of the study, the local fishers' assistance was much appreciated.
Funding
No funding was received to assist with the preparation of this manuscript
Author information
Authors and Affiliations
Contributions
S.J. collected and analysed the data, and prepared the draft; N.T.S. conceptualized and supervised the research work, edited the manuscript and approved the final version of the research article; D.B. supervised the research work and analysis, and edited the manuscript; C.J. involved in analysis of data.
Corresponding author
Ethics declarations
Competing Interests
The authors declare no competing interests.
Ethical Approval
All the research meets the ethical guidelines including adherence to the legal requirements of India
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Jana, S., Srinivasan, N.T., Bhakta, D. et al. Population Age Structure and Stock Assessment of Reeve’s Croaker Chrysochir aurea (Richardson, 1846) Along West Bengal Coast of India. Thalassas 40, 835–845 (2024). https://doi.org/10.1007/s41208-024-00671-9
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s41208-024-00671-9