Research Article
First Report on Temporal Variation of Conditions of Clupisoma garua in the Ganges River Through Multiple Functions
Taiba Akter Laboni1, Md. Akhtar Hossain1,2, Mst. Shahinur Khatun1,2, Md. Golam Sarwar1,2, Nur-E-Farjana Ilah1, Kamruzzaman1,2, Tasnim Akter Akhi1,2, Mst. Meherun Nesa1,2 and Md. Yeamin Hossain1*
1Department of Fisheries, University of Rajshahi, Rajshahi 6205, Bangladesh; 2Institute of Natural Resources Research and Development, Rajshahi 6206, Bangladesh.
Abstract | The Garua bacha, scientifically known as Clupisoma garua, is a fish species of significant commercial and nutritional value. This research presents the initial exploration of condition factors, including Fulton’s condition factor (KF), allometric condition factor (KA), relative condition factor (KR) and relative weight (WR) of Clupisoma garua in the Ganges River, northwestern region of Bangladesh using 12-months data. A total of 1200 individuals (630 male and 570 female) were taken from May 2017 to April 2018. Body weight (BW) and the total length (TL) were determined using a digital scale and measuring board, respectively, with an accuracy of 0.01 g and 0.01 cm. LFD showed TL for males ranged from 3.8 to 25.9 cm, while for females, it ranged from 3.9-26.3 cm. The report showed negative allometric growth of this species. KF values of males were 0.511 to 1.713, while females ranged from 0.519 to 1.669. In contrast, KA fluctuated from 0.034-0.004 for male and 0.032-0.004 for female individuals. Moreover, KR ranged from 0.845-1.312 for male and 0.873-1.447 for female individuals. Yet, WR for male sexes ranged from 39.89-131.18 and 83.67-129.28 for females. The KF values of male and female C. garua exhibit a significant correlation with TL and BW relationships. The mean relative weight (WR) which indicating an imbalanced condition between food supply and predators for this species. Male and female sexes of C. garua had form factors (a3.0) of 0.0061 and 0.0063 respectively, indicating the fish was elongated. Consequently, this study will provide valuable insights for fisheries biologists and environmentalists to establish sustainable management practices for C. garua in the Ganges River and its adjacent environs.
Received | May 11, 2023; Accepted | May 08, 2025; Published | October 09, 2025
*Correspondence | Md. Yeamin Hossain, Department of Fisheries, University of Rajshahi, Rajshahi 6205, Bangladesh; Email: [email protected]
Citation | Laboni, T.A., M.A. Hossain, M.S. Khatun, M.G. Sarwar, N.F. Ilah, Kamruzzaman, T.A. Akhi, M.M. Nesa and M.Y. Hossain. 2025. First report on temporal variation of conditions of Clupisoma garua in the ganges river through multiple functions. Sarhad Journal of Agriculture, 41(4): 1481-1493.
DOI | https://dx.doi.org/10.17582/journal.sja/2025/41.4.1481.1493
Keywords | Condition factors, Ganges River, Clupisoma garua, Form factor, Growth
Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Introduction
The Garua Bachcha, scientifically referred to as Clupisoma garua belongs to the Schilbeidae family within the order Siluriformes (Ullah, 2022). The Garua Bachcha commonly known as the Ghaura or the Muribacha in the country of Bangladesh (Table 1). The geographic distribution of C. garua encompasses India, Bangladesh, Pakistan, Nepal and Burma (Bhuiyan, 1964; Day, 1878; Jayaram, 1981; Mishra, 1959; Talwar and Jhingran, 1991). This species is predominantly encountered in lacustrine environments, which may typically be found in bigger rivers and reservoirs, as well as in impoundments that are not moving. The majority of this species habitats are freshwater, where it lives as a bottom-dwelling species; however, brackish water abundance has also been reported. According to Verma and Serajuddin (2017), C. garua is commonly observed moving in cohesive groups referred to as shoals, traversing various waterways such as canals, Rivers, streams, lakes, reservoirs and swamplands. These water bodies encompass both freshwater and brackish water environments. According to Nikolsky (1963), C. garua is categorized as a euryphagous fish. According to Nath (1994), this species of fish is extremely carnivorous and predatory in its natural environment. All types of consumers eat this fish, but low-income individuals are the most likely to do so because of the fish’s high nutritional value. C. garua contains approximately 18.40% protein, 5.2% fat and 74.2% water content, making it a valuable food source (Bhuiyan, 1964; Memon et al., 2010). Moreover, this species is recognized for its pleasant flavor (Siddik et al., 2016; Verma and Serajuddin, 2017). Although the IUCN Red List Status classifies the species as Least Concern (IUCN, 2022), Bangladesh considers it to be endangered and takes necessary conservation measures (IUCN, 2015).
Table 1: Common names and country list of Clupisoma garua.
|
Common name |
Country |
Language |
|
Garua bachcha |
Global |
English |
|
River catfish |
Bangladesh |
English |
|
Ghaura/ Gang gaira |
Bangladesh |
Bengali |
|
Sillimoni |
Finland |
Finnish |
|
Neria |
India |
Assamese |
|
Garua bachcha |
India |
English |
The length-frequency distribution (LFD) is a fundamental biometric tool widely used in various ecological and fisheries studies. It is instrumental in calculating growth rates, determining growth performance indices, and assessing fish mortality rates (Neuman and Allen, 2001). Additionally, LFD is critical for evaluating river health by estimating residual biomass and identifying breeding seasons (Laboni et al., 2024b; Ranjan et al., 2005). It also supports comparative analyses of physical traits among different species and examines population dynamics of a single species across diverse aquatic ecosystems (Ilah et al., 2023).
Moreover, length-weight relationships (LWRs) are significant biometric indicators used to compare and analyze various biological conditions. They are particularly valuable as they enable the estimation of weight based on length measurements, which is especially useful when direct weight measurements in the field are impractical or time-consuming. The parameters obtained from LWRs play a critical role in fish biology, offering valuable insights into the status of fish stocks (Khatun et al., 2023; Laboni et al., 2024a). Additionally, LWRs serve as an essential tool for understanding population growth patterns and dynamics.
The condition factor is commonly calculated to assess the overall health, productivity, and physiological state of fish populations (Richter, 2007). It also offers valuable information about physiological condition, such as body shape, lipid content, and growth rates (Froese, 2006; Rypel and Richter, 2008). Among these metrics, the relative condition factor (KR) remains a practical and widely used tool for biologists and fisheries managers to evaluate the health of fish stocks. Additionally, morphometric relationships, such as length-weight relationships (LWRs), along with relative condition factor (KR), Fulton’s condition factor (KF), and allometric condition factor (KA), are key biological parameters for studying condition or health status of fish populations. The relative weight (WR) approach is frequently utilized to analyze fish populations within specific ecosystems, particularly in understanding their roles as either prey or predator (Rypel and Richter, 2008). Furthermore, variations in body shape among different fish species or populations can be identified using the form factor (Froese, 2006).
The author acknowledges a limited number of studies conducted on C. garua, with notable examples including research on the variation in the life history of this Schilbid catfish species in coastal waters (Siddik et al., 2016), the length weight relationship (Sani et al., 2016), the impact of gonadal weight on length weight relationship (Akter et al., 2019), modes of reproduction (Breder et al., 1966) and genetic characterization (Sarawat et al., 2013) (Table 2).
Table 2: Available work on different aspects of Clupisoma garua world wide.
|
Aspects |
Habitat /Country |
References |
|
Length weight relationship |
Gomti River, India |
Sani et al. (2016) |
|
Impact of Gonad weight on the length weight relationships |
Old Brahmaputra River, Bangladesh |
Akter et al. (2019) |
|
Modes of reproduction |
Neptune City, New Jersey |
Breder et al. (1966) |
|
Genetic characterization |
Ganga, Gomti, Betwa, Gandak and Brahmaputra, India |
Sarawat et al. (2014) |
|
A Comprehensive Impression |
Bangladesh |
Ullah (2022) |
|
Variation in the life-history traits of a Schilbid catfi sh |
coastal waters of southern Bangladesh |
Siddik et al. (2017) |
|
Stock Structure |
southern coastal zone of Bangladesh |
Nahar et al. (2017) |
There is an immediate need to manage and control of the numerous distinct stocks of C. garua in the investigated region since this species is crucial to small-scale inland capture fisheries. Consequently, the purpose of this research is to provide a comprehensive description of C. garua by examining its various functional aspects and condition factors, encompassing KF, KA, KR and WR based on twelve months of repeated sampling effort conducted in the Ganges River of Bangladesh.
Materials and Methods
Sampling and measurement
This research was conducted in the Nawabganj area of northern Bangladesh, which is located at a latitude of 24° 65’ N and a longitude of 88° 06’ E. (These coordinates may be found on a map) (Figure 1). From May 2017 to April 2018, monthly sampling were done on the individuals (C. garua) from a variety of locations in Rajshahi, in the Northwestern region of Bangladesh. These locations included Godagari, Shaheb Bazar, Jahajghat, Charghat and Yusufpur, as well as Bagha. The fish specimens were captured using traditional fishing equipment, including cast nets, Seine nets and gill nets. To preserve their freshness, after being immediately frozen with ice at the location, the specimens were transported to the laboratory where they were fixed in a solution of formalin containing 5% to ensure proper fixation. The necessary length measurements of each individual were taken using digital slide calipers with an accuracy of up to 0.01 cm, while their body weight was recorded using an electric balance with a precision of 0.01 g. These meticulous measurement techniques were employed to ensure accurate and precise data collection, enabling comprehensive analyses and investigations in the laboratory environment.
Length–frequency distribution (LFD)
The estimation of fish age and growth necessitates the utilization of length-frequency distributions. To analyze the C. garua population, the length-frequency distributions (LFD) were utilized, whereby the total length (TL) was compared within 1.0 cm class intervals.
Length-weight relationships (LWR)
The length-weight relationship was determined using the following equation: BW = a*(TL)b, where BW represents A total body weight measured in grams, and TL corresponds to A total length measured in centimeters. To calculate the parameters a and b in the linear regression analysis, natural logarithms were utilized: ln (BW)= ln (a) + b ln (BW) (TL). In accordance with Froese’s Research (2006), the regression analysis was conducted after excluding severe outliers.
Condition factors
Various formulas were employed to assess the condition factor in different studies. Fulton’s condition factor, based on the equation proposed by Fulton (1904), can be calculated as follows: KF = 100 (W/L3); while W represents the weight of the whole body in grams, and L represents the total length in centimeters. The scaling factor of 100 is applied to standardize KF. To determine the relative condition factor (KR), (Le Cren, 1951) equation is utilized: KR = W/(a*Lb); where W denotes the body weight, L represents the total length and a and b are the parameters for length-weight relationships (LWR). Tesch’s equation from 1968 is employed to obtain the allometric condition factor, KA = W/Lb; where W is the weight of the body, L is the total length and b is the parameter for LWR. The relative weight (WR) can be derived using Froese’s formula: WR is calculated as W = (W/WS) * 100; where W represents the observed body weight of an individual and WS is the prospective standard body weight for the similar species. WS is calculated using the equation: WS = a * Lb, where a and b are the parameters for TL and BW relations.
Form factor (a3.0)
The formula presented by Froese (2006) was utilized to determine the form factor for C. garua as follows: a3.0 = 10log a – s (b-3). In this equation, a and b represent LWRs parameters, while s denotes the slope of the regression line that compares the natural logarithm of a to b. However, due to insufficient data on LWRs for this particular species, it was not feasible to calculate the regression (S) of ln a vs. b accurately. Consequently, an average slope of -1.358 was employed as an approximation in this analysis to estimate the form factor. This approach was done so that the form factor could be calculated. This was done due to the necessity of having adequate evidence on LWRs in order to determine the regression (S) of ln a vs. b.
Statistical analysis
Graph Pad Prism 8.0 was used for statistical analysis. The relationships between condition factors with TL and BW was investigated through the utilization of the Spearman rank correlation test. In order to distinguish it from average relative weight (WR), which is set at 100, a Wilcoxon sign-ranked test was conducted (Anderson and Neumann, 1996). Every single statistical test was run at a significance level of 5% (p < 0.05), which is the accepted standard. This approach ensured that the analysis remained independent and unbiased, allowing for a comprehensive examination of the relationship between the condition factors with the variables TL and BW.
Results
Length–frequency distribution
Fishers on the Ganges River in Northern Bangladesh supplied us with 1200 fish specimens that we randomly gathered on occasion. Table 3 provides a summary of the length and weight measurements for C. garua, along with their corresponding 95% confidence intervals (CI). The statistical data presented in this table offer valuable insights into the characteristics of the species. During the investigation, the TL ranged from around 3.8 to 25.9 centimeters for males, 3.9 to 26.3 centimeters for females, while the BW ranged from around 19.5 to 106.57 grams for males and 20.07 to 125.41 grams for females. In accordance with length frequency distribution, the TL size that ranged from 15.99 to 17.99 centimeters had a statistically top ranking for the male individual (Figure 2); whereas the TL size that ranged from 14.99 to 17.99 centimeters had a statistically top ranking for the female individual.
Table 3: Descriptive statistics on the length (cm) and weight (g) measurement of C. garua.
|
Measurement |
n |
Min |
Max |
Mean ± SD |
95% CL |
|
|
Male |
TL |
1200 |
3.8 |
25.9 |
11.39±3.81 |
10.41-12.37 |
|
19.75±3.26 |
18.85-20.64 |
|||||
|
BW |
0.94 |
106.57 |
52.83±24.26 |
46.14-59.52 |
||
|
25.65±21.11 |
20.25-31.06 |
|||||
|
Female |
TL |
1200 |
3.9 |
26.3 |
11.46±3.86 |
10.21-12.71 |
|
21.10±3.44 |
20.09-22.11 |
|||||
|
BW |
0.99 |
125.41 |
66.37±29.50 |
57.71-75.03 |
||
|
26.51±24.79 |
18.48-34.54 |
|||||
Length-weight relationships (LWRs)
Table 4 and Figure 3 present an important information regarding the sample size (n), regression parameters
Table 4: Descriptive statistics and estimated parameters of the length-weight relationships (BW = a × TLb) of the Clupisoma garua (Hamilton, 1822) in the Ganges river, Northwestern Bangladesh.
|
Month |
Sex |
N |
Regression parameters |
95% CL of a |
95% CL of b |
r2 |
GT |
|
|
a |
b |
|||||||
|
May |
M |
53 |
0.0295 |
2.52 |
0.0221-0.0395 |
2.41-2.62 |
0.980 |
-A |
|
F |
47 |
0.0189 |
2.66 |
0.0142-0.0251 |
2.56-2.76 |
0.985 |
-A |
|
|
June |
M |
45 |
0.0060 |
3.03 |
0.0047-0.0078 |
2.94-3.11 |
0.991 |
I |
|
F |
55 |
0.0147 |
2.72 |
0.0115-0.0189 |
2.64-2.80 |
0.980 |
-A |
|
|
July |
M |
43 |
0.0084 |
2.91 |
0.0067-0.0104 |
2.84-2.98 |
0.992 |
-A |
|
F |
57 |
0.0092 |
2.89 |
0.0068-0.0123 |
2.80-2.99 |
0.988 |
-A |
|
|
August |
M |
45 |
0.0070 |
3.00 |
0.0051-0.0095 |
2.90-3.11 |
0.987 |
I |
|
F |
55 |
0.0108 |
2.85 |
0.0082-0.0142 |
2.76-2.94 |
0.986 |
-A |
|
|
September |
M |
56 |
0.0303 |
2.69 |
0.0271-0.0339 |
2.64-2.73 |
0.996 |
-A |
|
F |
44 |
0.0203 |
2.83 |
0.0188-0.0220 |
2.80-2.87 |
0.998 |
-A |
|
|
October |
M |
52 |
0.0100 |
2.84 |
0.0082-0.0122 |
2.76-2.91 |
0.990 |
-A |
|
F |
48 |
0.0087 |
2.89 |
0.0069-0.0109 |
2.81-2.98 |
0.989 |
-A |
|
|
November |
M |
56 |
0.0097 |
2.83 |
0.0081-0.0116 |
2.76-2.90 |
0.993 |
-A |
|
F |
44 |
0.0088 |
2.87 |
0.0073-0.0106 |
2.80-2.93 |
0.994 |
-A |
|
|
December |
M |
51 |
0.0050 |
3.07 |
0.0041-0.0059 |
3.01-3.14 |
0.995 |
I |
|
F |
49 |
0.0044 |
3.12 |
0.0036-0.0053 |
3.05-3.19 |
0.993 |
+A |
|
|
January |
M |
54 |
0.0098 |
2.82 |
0.0079-0.0122 |
2.74-2.90 |
0.989 |
-A |
|
F |
46 |
0.0088 |
2.87 |
0.0069-0.0111 |
2.78-2.95 |
0.990 |
-A |
|
|
February |
M |
52 |
0.0076 |
2.95 |
0.0056-0.0103 |
2.83-3.06 |
0.983 |
-A |
|
F |
48 |
0.0135 |
2.72 |
0.0097-0.0188 |
2.76-2.84 |
0.979 |
-A |
|
|
March |
M |
51 |
0.0278 |
2.51 |
0.0203-0.0380 |
2.40-2.62 |
0.977 |
-A |
|
F |
49 |
0.0213 |
2.59 |
0.0154-0.0296 |
2.48-2.70 |
0.978 |
-A |
|
|
April |
M |
52 |
0.0090 |
2.90 |
0.0074-0.0110 |
2.83-2.96 |
0.993 |
-A |
|
F |
48 |
0.0217 |
2.59 |
0.0179-0.0265 |
2.52-2.66 |
0.992 |
-A |
|
M, Male; F, Female; n, Sample Size; a, Intercept; b, Slope ; CL, 95% confidence limit; GT, growth type.
of length-weight relationships along with their 95% confidence limits (CL) and determination of coefficient. Also, these studies clarify the development pattern of C. garua (r2). Estimated values of b were indicated that this species had an allometric growth pattern (TL vs. BW).
Fulton’s condition factor (KF)
The lowest KF standard for males was 0.511 in December when the highest possible standard was 1.713 in September (Table 5 and Figure 4). On the other side, the lowest possible KF value for females was 0.519 in December, while the highest possible value was 1.669 in September. Significant differences in KF (condition factor) were observed between male and female individuals during the research work.
Relative condition factor (KR)
Relative condition factor for males ranged from a high of 1.312 in October to a low of 0.845 in December. As opposed to, the lowest KR values for female sexes were 0.837 during the months of October and the highest KR value was 1.447 in January (Table 6). Mann-Whitney U-test (non-parametric) revealed statistically variations in KR between male and female sexes. These findings indicate notable variations in the condition of male and female individuals.
Relative weight (WR)
The lowest and highest values of WR for male sexes occurred in the months of June and October, respectively. These values were 39.89 and 131.18 (Table 7 and Figure 5). On the other end, the lowest and highest potential WR for females during the month of October were 83.67 and 129.28 respectively. The results of the one-sample t-test demonstrated a significant deviation of the relative weight from 100 for both male and female individuals.
Table 5: Descriptive statistics on Fulton’s condition factor (KF) measurements and their 95% confidence limits of the Clupisoma garua (Hamilton, 1822) in the Ganges river, Northwestern Bangladesh.
|
Month |
Sex |
n |
Fulton’s condition factor (KF) |
|||
|
Min |
Max |
Mean ± SD |
95% CL |
|||
|
May |
M |
53 |
0.665 |
0.860 |
0.7389±0.0483 |
0.7246-0.7512 |
|
F |
47 |
0.662 |
0.808 |
0.7173±0.0330 |
0.7076-0.7270 |
|
|
June |
M |
45 |
0.593 |
0.732 |
0.6576±0.0305 |
0.6489-0.6663 |
|
F |
55 |
0.576 |
0.713 |
0.6342±0.0411 |
0.6225-0.6459 |
|
|
July |
M |
43 |
0.596 |
0.706 |
0.6400±0.0300 |
0.6317-0.6483 |
|
F |
57 |
0.573 |
0.759 |
0.6607±0.0383 |
0.6494-0.6719 |
|
|
August |
M |
45 |
0.625 |
0.776 |
0.7055±0.0405 |
0.6929-0.7182 |
|
F |
55 |
0.611 |
0.772 |
0.6879±0.0421 |
0.6769-0.6990 |
|
|
September |
M |
56 |
1.080 |
1.713 |
1.4447±0.1754 |
1.3998-1.4896 |
|
F |
44 |
1.170 |
1.669 |
1.3716±0.0985 |
1.3397-1.4035 |
|
|
October |
M |
52 |
0.566 |
0.878 |
0.6500±0.0678 |
0.6422-0.6778 |
|
F |
48 |
0.570 |
0.870 |
0.6605±0.0705 |
0.6400-0.6809 |
|
|
November |
M |
56 |
0.537 |
0.718 |
0.6129±0.0440 |
0.6011-0.6247 |
|
F |
44 |
0.545 |
0.741 |
0.6049±0.0422 |
0.5921-0.6177 |
|
|
December |
M |
51 |
0.511 |
0.673 |
0.6102±0.0322 |
0.6008-0.6196 |
|
F |
49 |
0.519 |
0.696 |
0.6135±0.0411 |
0.6021-0.6250 |
|
|
January |
M |
54 |
0.551 |
0.715 |
0.6040±0.0378 |
0.5938-0.6142 |
|
F |
46 |
0.537 |
0.706 |
0.6032±0.0350 |
0.5927-0.6138 |
|
|
February |
M |
52 |
0.579 |
0.746 |
0.6543±0.0425 |
0.6425-0.6661 |
|
F |
48 |
0.549 |
0.736 |
0.6291±0.0506 |
0.6144-0.6438 |
|
|
March |
M |
51 |
0.583 |
0.771 |
0.6800±0.0524 |
0.6653-0.6948 |
|
F |
49 |
0.573 |
0.755 |
0.6584±0.0524 |
0.6434-0.6735 |
|
|
April |
M |
52 |
0.626 |
0.718 |
0.6724±0.0222 |
0.6663-0.6786 |
|
F |
48 |
0.576 |
0.765 |
0.6689±0.0443 |
0.6561-0.6818 |
|
M, Male; F, Female; Min, Minimum; Max, Maximum; SD, Standard Deviation.
Allometric condition factor (KA)
Allometric condition factor (KA) values ranged from high of 0.034 in September to low of 0.004 in December for male sexes (Table 8). The lowest KA values for female was 0.032 in May to the highest value was 0.004 in December. Using a non-parametric Mann-Whitney U-test, we found that KA differed significantly between male and female individuals (Table 9).
Form factor (a3.0)
Table 10 presents the calculated form factors (a3.0) for male and female fish in the Ganges River, located in northwestern Bangladesh. The form factor was determined to be 0.0061 for male individuals and 0.0063 for female individuals. These results provide important information regarding the body shape and proportions of the studied fish populations.
Discussion
There is very little information on the condition factor of C. garua that can be found in any of the existing literature from Bangladesh or anywhere else. As a result, the current study is the first attempt to define the temporal variation of conditions of C. garua originating from the Ganges River, northwestern in Bangladesh, including LFD, LWR, and a3.0. During the twelve-month sampling period, we collected a total of 1200 specimens of different body sizes using locally available equipment. Out of these, 630 specimens were male, and 570 specimens were female.
In total, 1200 specimens of varying body sizes were sampled for doing this particular research. Nevertheless, it proved troublesome to collect fishes lower than 3.8 cm and larger than 26.3 cm in length. This may be because fishers did not use the appropriate
Table 6: Descriptive statistics on Relative condition factor (KR) measurements and their 95% confidence limits of the Clupisoma garua (Hamilton, 1822) in Ganges river, northwestern Bangladesh.
|
Month |
Sex |
n |
Relative condition factor (KR) |
|||
|
Min |
Max |
Mean ± SD |
95% CL |
|||
|
May |
M |
53 |
0.925 |
1.086 |
1.0022±0.0384 |
0.9917-1.0128 |
|
F |
47 |
0.946 |
1.081 |
1.0002±0.0317 |
0.9909-1.0095 |
|
|
June |
M |
45 |
0.908 |
1.123 |
1.003±0.0465 |
0.9893-1.0157 |
|
F |
55 |
0.899 |
1.081 |
1.000±0.0454 |
0.9867-1.0126 |
|
|
July |
M |
43 |
0.921 |
1.103 |
0.9982±0.0446 |
0.9859-1.0105 |
|
F |
57 |
0.870 |
1.138 |
0.9975±0.0544 |
0.9815-1.0103 |
|
|
August |
M |
45 |
0.870 |
1.082 |
0.9821±0.0564 |
0.9645-0.9996 |
|
F |
55 |
0.893 |
1.089 |
1.0007±0.0556 |
0.9861-1.0153 |
|
|
September |
M |
56 |
0.839 |
1.109 |
1.0021±0.0624 |
0.9851-1.0180 |
|
F |
44 |
0.901 |
1.116 |
1.0029±0.0362 |
0.9911-1.0146 |
|
|
October |
M |
52 |
0.848 |
1.312 |
1.0026±0.0887 |
0.9793-1.0259 |
|
F |
48 |
0.837 |
1.293 |
1.0006±0.0983 |
0.9721-1.0292 |
|
|
November |
M |
56 |
0.859 |
1.128 |
1.0022±0.0580 |
0.9867-1.0118 |
|
F |
44 |
0.871 |
1.201 |
0.9977±0.0580 |
0.9801-1.0154 |
|
|
December |
M |
51 |
0.845 |
1.104 |
0.9942±0.0500 |
0.9796-1.0087 |
|
F |
49 |
0.865 |
1.143 |
0.9933±0.0609 |
0.9764-1.0103 |
|
|
January |
M |
54 |
0.905 |
1.154 |
0.9995±0.0525 |
0.9853-1.0137 |
|
F |
46 |
0.891 |
1.447 |
0.9976±0.0514 |
0.9822-1.0131 |
|
|
February |
M |
52 |
0.872 |
1.130 |
0.9981±0.0640 |
0.9803-1.0160 |
|
F |
48 |
0.873 |
1.125 |
1.0044±0.0662 |
0.9851-1.0236 |
|
|
March |
M |
51 |
0.888 |
1.088 |
1.0000±0.0474 |
0.9867-1.0133 |
|
F |
49 |
0.856 |
1.109 |
1.0030±0.0541 |
0.9875-1.0185 |
|
|
April |
M |
52 |
0.947 |
1.0702 |
1.0057±0.0304 |
0.9972-1.0142 |
|
F |
48 |
0.922 |
1.0673 |
1.0026±0.0322 |
0.9933-1.0120 |
|
M, male; F, female; Min, minimum; Max, maximum; SD, standard deviation.
gear or because they skipped out the areas where larger fish are found (Hossain et al., 2016). According to Hossain and Ohtomi (2010), it is plausible that alterations in size could be attributed to fluctuations in environmental conditions, including water temperature and appearance of food. In the context of this research, the maximum total length (TL) observed for male C. garua was 25.9 cm, while for female it was 26.3 cm. Notably, these measurements are comparatively smaller than the highest documented TL values of 36.6 cm in the Betwa and Gomti Rivers in Karnataka and Uttar Pradesh, India (Sani et al., 2016), as well as 33 cm in the Gomti River in India (Kumar et al., 2014). Based on the results obtained from this investigation, the highest weight recorded for male specimens reached 106.57 g, while for female it reached 125.41 g. Nevertheless, it should be noted that the greatest body weight documented in coastal regions of Bangladesh was 128.80 g (Siddik et al., 2016). The assessment of the highest length of an individual holds paramount importance in the context of fisheries resource development and management (Hossain and Othomi, 2010).
Table 7: Descriptive statistics on Relative Weight (WR) measurements and their 95% confidence limits of the Clupisoma garua (Hamilton, 1822) in the Ganges river, Northwestern Bangladesh.
|
Month |
Sex |
n |
Relative weight (WR) |
|||
|
Min |
Max |
Mean ± SD |
95% CL |
|||
|
May |
M |
53 |
92.46 |
108.60 |
100.22±3.84 |
99.17-101.28 |
|
F |
47 |
94.63 |
108.06 |
100.02±3.17 |
99.09-100.95 |
|
|
June |
M |
45 |
39.89 |
49.22 |
44.15±2.05 |
43.57-44.74 |
|
F |
55 |
61.75 |
74.13 |
68.41±3.13 |
67.52-69.30 |
|
|
July |
M |
43 |
92.13 |
110.28 |
99.82±4.46 |
98.59-101.05 |
|
F |
57 |
86.99 |
116.81 |
99.75±5.44 |
98.15-101.34 |
|
|
August |
M |
45 |
88.23 |
109.69 |
99.64±5.72 |
97.85-101.42 |
|
F |
55 |
89.28 |
109.84 |
100.07±5.56 |
98.61-101.53 |
|
|
September |
M |
56 |
83.95 |
110.90 |
100.21±6.24 |
98.61-101.80 |
|
F |
44 |
90.13 |
111.64 |
100.29±3.62 |
99.11-101.46 |
|
|
October |
M |
52 |
84.85 |
131.18 |
100.26±8.87 |
97.93-102.59 |
|
F |
48 |
83.67 |
129.28 |
100.06±9.83 |
97.21-102.92 |
|
|
November |
M |
56 |
85.93 |
112.85 |
100.22±5.80 |
98.67-101.78 |
|
F |
44 |
87.12 |
120.09 |
99.77±5.80 |
98.01-101.54 |
|
|
December |
M |
51 |
84.55 |
110.40 |
99.42±5.00 |
97.96-100.87 |
|
F |
49 |
86.52 |
114.30 |
99.33±6.09 |
97.64-101.03 |
|
|
January |
M |
54 |
90.48 |
115.37 |
99.95±5.25 |
98.53-101.37 |
|
F |
46 |
89.08 |
114.70 |
99.76±5.14 |
98.22-101.31 |
|
|
February |
M |
52 |
87.23 |
112.99 |
99.81±6.40 |
98.03-101.60 |
|
F |
48 |
87.31 |
112.47 |
100.44±6.62 |
98.51-102.36 |
|
|
March |
M |
51 |
88.76 |
108.76 |
100.00±4.74 |
98.67-101.34 |
|
F |
49 |
85.56 |
110.86 |
100.30±5.41 |
98.75-101.85 |
|
|
April |
M |
52 |
94.69 |
107.02 |
100.57±3.04 |
99.72-101.42 |
|
F |
48 |
92.21 |
106.73 |
100.26±3.22 |
99.33-101.20 |
|
M, male; F, female; Min, minimum; Max, maximum; SD, standard deviation.
Stock condition can be evaluated using the growth parameter. The b value in the study was within the range of 2.5 to 3.5, which is consistent with the literature (Froese, 2006). According to Tesch (1971), when the b value is equal to 3, it indicates isometric growth. If the b value is greater than 3, positive allometric growth is observed, while b value is lower than 3 indicates negative allometric growth. Allometric coefficient b value of LWRs for C. garua was found to be 2.71, 2.80 and for male and female, indicating the negative allometric growth, while discussing the length-weight relationships of C. garua, it is worth noting that Sani et al. (2016) reported the b value of 3.10 for the similar individuals in the Gomti River in India. Conversely, Kumar et al. (2014) observed b value of 2.69 for the same individual in similar water body. Siddik et al. (2016) indicated that the b value for male in coastal water body of Bangladesh was 2.955, whereas for female it was 2.893. It is widely recognized that several variables impact the relationships of LWR in fish. These variables encompass the growth cycle, sex, season, rations (including quantity, quality and shaped), maturity stage, overall fish health and condition, conservation techniques and disparities in the noticed length ranges of captured individuals (Tesch, 1971; Hossain et al., 2013a). Yet, it is noteworthy that none of these variables were accepted into account in the present investigation.
Table 8: Descriptive statistics on Allometric condition factor (KA) measurements and their 95% confidence limits of the Clupisoma garua (Hamilton, 1822) in the Ganges river, Northwestern Bangladesh.
|
Month |
Sex |
n |
Allometric condition factor (KA) |
|||
|
Min |
Max |
Mean ± SD |
95% CL |
|||
|
May |
M |
53 |
0.027 |
0.0320 |
0.0296±0.0011 |
0.0293-0.0299 |
|
F |
47 |
0.020 |
0.0320 |
0.0214±0.0007 |
0.0212-0.0216 |
|
|
June |
M |
45 |
0.006 |
0.007 |
0.0064±0.0003 |
0.0063-0.0065 |
|
F |
55 |
0.012 |
0.015 |
0.0135±0.0006 |
0.0134-0.0137 |
|
|
July |
M |
43 |
0.008 |
0.009 |
0.0084±0.0004 |
0.0083-0.0085 |
|
F |
57 |
0.008 |
0.010 |
0.0092±0.0005 |
0.0090-0.0093 |
|
|
August |
M |
45 |
0.006 |
0.008 |
0.0070±0.0004 |
0.0069-0.0071 |
|
F |
55 |
0.010 |
0.011 |
0.0108±0.0006 |
0.0107-0.0110 |
|
|
September |
M |
56 |
0.025 |
0.034 |
0.0304±0.0019 |
0.0299-0.0308 |
|
F |
44 |
0.018 |
0.023 |
0.0204±0.0007 |
0.0201-0.0206 |
|
|
October |
M |
52 |
0.008 |
0.013 |
0.0100±0.0009 |
0.0098-0.0103 |
|
F |
48 |
0.007 |
0.011 |
0.0087±0.0009 |
0.0084-0.0090 |
|
|
November |
M |
56 |
0.008 |
0.011 |
0.0097±0.0006 |
0.0096-0.0099 |
|
F |
44 |
0.008 |
0.011 |
0.0088±0.0005 |
0.0086-0.0089 |
|
|
December |
M |
51 |
0.004 |
0.006 |
0.0050±0.0003 |
0.0049-0.0050 |
|
F |
49 |
0.004 |
0.005 |
0.0044±0.0003 |
0.0043-0.0044 |
|
|
January |
M |
54 |
0.009 |
0.011 |
0.0098±0.0005 |
0.0097-0.0099 |
|
F |
46 |
0.008 |
0.010 |
0.0088±0.0005 |
0.0086-0.0089 |
|
|
February |
M |
52 |
0.007 |
0.009 |
0.0076±0.0005 |
0.0075-0.0077 |
|
F |
48 |
0.012 |
0.016 |
0.0136±0.0010 |
0.0133-0.0138 |
|
|
March |
M |
51 |
0.025 |
0.030 |
0.0278±0.0013 |
0.0274-0.0282 |
|
F |
49 |
0.018 |
0.024 |
0.0214±0.0012 |
0.0210-0.0217 |
|
|
April |
M |
52 |
0.009 |
0.010 |
0.0091±0.0003 |
0.0090-0.0091 |
|
F |
48 |
0.020 |
0.023 |
0.0218±0.0006 |
0.0216-0.0220 |
|
M, male; F, female; Min, minimum; Max, maximum; SD, standard deviation.
Table 9: Relationships of condition factor with total length and body weight of Clupisoma garua in the Ganges river, northwestern Bangladesh.
|
Relationships |
Sex |
rs values |
95% CL of rs |
P values |
Significance |
|
TL vs. KA |
M |
0.2589 |
0.282-0.332 |
P = 0.001 |
* |
|
TL vs. KF |
-0.232 |
-0.39 to -0.15 |
P < 0.001 |
*** |
|
|
TL vs. KR |
0.2798 |
0.2040-3523 |
P = 0.003 |
* |
|
|
TL vs. WR |
0.2796 |
0.2037-0.35 |
P = 0.003 |
* |
|
|
BW vs. KA |
0.3525 |
0.2800-4210 |
P = 0.015 |
ns |
|
|
BW vs. KF |
-0.115 |
-1940 to-0.03 |
P < 0.001 |
*** |
|
|
BW vs. KR |
0.3875 |
0.3169-0.453 |
P = 0.005 |
* |
|
|
BW vs. WR |
0.3872 |
0.3116-0.4535 |
P = 0.001 |
* |
|
|
TL vs. KA |
F |
0.1615 |
-0.24 to -0.07 |
P = 0.001 |
* |
|
TL vs. KF |
-0.224 |
-0.30 to -0.14 |
P < 0.001 |
*** |
|
|
TL vs. KR |
0.2177 |
0.1357-0.296 |
P = 0.003 |
* |
|
|
TL vs. WR |
0.2166 |
0.1345-0.2958 |
P = 0.004 |
* |
|
|
BW vs. KA |
-0.161 |
-0.24 to -0.07 |
P < 0.001 |
*** |
|
|
BW vs. KF |
-0.124 |
-0.204 to -0.03 |
P < 0.003 |
*** |
|
|
BW vs. KR |
0.3166 |
0.2385-0.3907 |
P = 0.035 |
ns |
|
|
BW vs. WR |
0.3156 |
0.2373-0.3897 |
P = 0.001 |
* |
ns, not significant; * significant; *** highly significant
Table 10: The calculated form factor, a3.0 =10 log a-s (b-3) for the C. garua of different habitats using available length-Weight relationship (LWR) parameters in the worldwide.
|
Water body |
Sex |
Regression parameter |
Form factor (a3.0) |
Reference |
|
|
a |
b |
||||
|
Gomti River, India |
Unsexed |
0.0056 |
3.10 |
0.0077 |
Sani et al. (2016) |
|
Coastal waters of southern Bangladesh |
Female |
0.0101 |
2.89 |
0.006 |
Siddik et al. (2017) |
|
Male |
0.0091 |
2.96 |
0.006 |
||
|
Ganges River, Bangladesh |
Female |
0.0118 |
2.80 |
0.0063 |
Present study |
|
Male |
0.0150 |
2.71 |
0.0061 |
||
According to Froese (2006), provided a calculation of a value of a3.0 is 0.01, suggesting that the body shape of the fish resembles an elongated cylinder. The fact that the a3.0 value for male and female individuals in the Ganges River is 0.0061 and 0.0063, indicates that the C. garua species in the Ganges River has an elongated body shape. As opposed to, Siddik et al. (2016) indicated that the a3.0 value for male and female individuals in coastal water body were 0.006 and 0.006 respectively. In accordance with findings of current research, this should be considered the first attempt to study C. garua in Ganges River, Bangladesh.
In the current study, various condition factor, namely KF, KR, KA and WR, were employed to evaluate the overall health and productivity of the C. garua population. To choose the most suitable condition factor, several condition factor were used. A fish population’s condition factor provides information about its health within its natural ecology (Hossain et al., 2013b; Ilah et al., 2024). Moreover, it unveils diverse of bio-ecological relationships, such as the level of well-being, maturity and feeding behavior in relation to habitat suitability (Hossen et al., 2019).
In addition, the condition factor is a widely used biological indicator that indicates the entire health of a fish population. This index was developed for fish (Richter, 2007). A higher value of the condition factor indicates that the fish are in better condition, as supported by studies conducted by Hossain et al. (2017) and Maurya et al. (2018). Conversely, a lower value suggests that the environmental conditions are less favorable, as observed by Blackwell et al. (2000).
Furthermore, the condition factor serves as a widely employed biological metric, serving as an indicator of the overall health of a fish stock. The origins of this index can be attributed to Richter’s (2007) regarding fish. When the condition factor exhibits a larger value, it suggests that the fish are in superior condition, as indicated by researches conducted by Hossain et al. (2017) and Maurya et al. (2018). Conversely, a lower value indicates the ambient situations are less friendly, as revealed by research conducted by Blackwell et al. (2000).
The Fulton’s Condition Factor (KF) is a widely used metric in fisheries science to assess the health, well-being, and nutritional status of fish populations. In this research, spearman rank correlation test discovered a strong and statistically significant association between the condition factor, specifically KF and both total length (TL) and body weight (BW) for both male and female specimens. Throughout the study, it was observed that Fulton’s condition factor (KF) exhibited significantly higher values during the months spanning August to October. Yet, it was shown that the most favorable conditions were present throughout the September for both male and female individuals. KF started rising after the month of May and kept doing so all the way through October. This may suggest that there are ample food reserves and a sustainable ecosystem state (Froese, 2006). According to the Le Cren (1951), the interplay among feeding habits, parasite diseases and physiological factors contributes to fluctuate the condition factor.
The relative weight (WR) of an aquatic habitat influences the recruitment pattern of a fisheries community, as stated by Shulman and Ogden (1987). Values exceeding 100 imply an abundance of prey or a low consistency of predators, when standards below 100 signify a scarcity of prey or a high density of predators (Froese, 2006; Hossain et al., 2024). We found that average WR for male and female individuals of C. garua were significantly different from 100, suggesting that ecosystem in the Ganges River is in an unbalanced state. Yet, in Bangladesh, this species of fish is listed as endangered (IUCN Bangladesh, 2015). Since the relative weight encompasses essential physiological aspects of life history trait, such as fat percentage and growth, it presents a reliable and convenient metric to evaluate health condition or well-being of fish populations. Additionally, it serves as a valuable tool to evaluate the population-level responses to ecosystem disturbances like climate change as revealed by research conducted by Rypel and Richter (2008). Furthermore, according to Offem et al. (2007), variations in food availability throughout different seasons can also affect these aspects.
In order to assess the health status of male and female participants within the resembling community, Froese (2006) suggested utilizing the relative condition factor (KR) among these factors. In the current investigation, did not permit comparisons between populations unless those populations shared a fundamentally similar relationships between TL and BW. Additionally, the use of Fulton’s condition factor, commonly referred to as KF, may prove beneficial since it is independent on the parameters a and b of the length-weight relationship (LWR). In this study, we examined the overall health conditions and productivity of C. garua by employing multiple condition factor, including KF, KR and KA.
Nevertheless, Siddik et al. (2016) documented that for the similar species in the coastal water body of southern Bangladesh, Fulton’s condition factor was indicative of a decline in feeding conditions within the coastal water body. Furthermore, they found that WR values were close to 100, suggesting a habitat characterized by a harmonious balance between supply of food and existence of predators (Anderson and Neumann, 1996). Yet, because it is first analysis of this species in the Ganges River, the results will serve as a baseline for comparison with subsequent studies.
Conclusions and Recommendations
This research provides fundamental data on the length-frequency distribution (LFD), length-weight relationships (LWRs), and form factor (a3.0) of C. garua, while establishing a critical baseline for its condition factors (KF, KA, KR, WR) in the Ganges River, Bangladesh. The findings reveal that KF values indicate most favorable conditions and high food reserves while WR, KR, and KA provide additional insights into its physiological condition. Notably, the study highlights negative allometric growth and males and females exhibiting elongated body shapes. The mean relative weight (WR) suggests an imbalance between food availability and predator pressure, underscoring the need for targeted conservation efforts. The findings equip fishery biologists, managers, and conservationists with essential tools to implement early management strategies and regulations, ensuring the sustainable conservation of C. garua populations in the Ganges River ecosystem. This research not only contributes to the scientific understanding of the species but also enhances the FishBase database, supporting global efforts in fisheries management and biodiversity conservation.
Acknowledgement
We express our sincere gratitude to the PIU-BARC-NATP-2 PBRG-156 for their valuable support and money they gave us. The people who helped collect the samples would also like to thank the fishers, whose names have been changed to protect their privacy, for their support and help.
Novelty Statement
This study provides the first comprehensive year-round assessment of Clupisoma garua in the Ganges River, revealing negative allometric growth, ecological imbalances, and an elongated body form, key insights for sustainable fisheries management and conservation.
Author’s Contribution
Taiba Akter Laboni: Data analysis and manuscript writing.
Md. Akhtar Hossain: Data collection and writing
Mst. Shahinur Khatun: Data analysis.
Md. Golam Sarwar: Data collection and analysis.
Nur-E-Farjana Ilah: Data analysis
Kamruzzaman: Data collection and analysis.
Tasnim Akter Akhi: Data analysis.
Mst. Meherun Nesa: Manuscript writing.
Md. Yeamin Hossain: Data analysis and edited the whole manuscript.
Conflict of interest
The authors have declared no conflict of interest.
References
Akter, Y., M.H.A. Hosen, M.I. Miah, Z.F. Ahmed, M.S. Chhanda, S.f Istiak and M. Shahriar. 2019. Impact of gonad weight on the length-weight relationships of River catfish (Clupisoma garua) in Bangladesh. Egypt. J. Aquat. Res., 45(4): 375-379. https://doi.org/10.1016/j.ejar.2019.10.003
Anderson, R.O. and R.M. Neumann. 1996. Length, weight, and associated structural indices. In: B.R. Murphy, D.W. Willis (Eds.), Fisheries Techniques, second ed., American Fisheries Society, Bethesda, Maryland, pp. 447–482.
Bhuiyan, A.L., 1964. Fishes of Dacca, Asiatic Society Pakistan. Publication 1, No. 13, Dacca, p. 71.
Blackwell, B.G., M.L. Brown and D.W. Willis. 2000. Relative weight (WR) status and current use in fisheries assessment and management. Rev. Fish. Sci., 8: 1–44. https://doi.org/10.1080/10641260091129161
Breder, C.M. and D.E. Rosen. 1966. Modes of reproduction in fishes. T.F.H. Publications, Neptune City, New Jersey, pp. 941.
Day, F., 1878. The fishes of India being a natural history of the fishes known to inhabit the seas and fresh waters of India, Burma and Ceylon. William Dowson and Sons, London. https://doi.org/10.5962/bhl.title.55567
Froese, R., 2006. Cube law, condition factor and weight-length relationships: History, meta-analysis and recommendations. J. Appl. Ichthyol., 22(4): 241-253. https://doi.org/10.1111/j.1439-0426.2006.00805.x
Fulton, T.W., 1904. The rate of growth of fishes. Twenty-second Annual Report. Part III. Fisheries Board of Scotland, Edinburgh, pp. 141-241.
Hossain, M.A., T.A. Laboni, M.S. Khatun, M.A. Rahman, M.A. Hossen, O. Rahman and M.Y. Hossain. 2024. Exploring the reproductive features of Clupisoma garua from Ganges River, Bangladesh: insights into eco-climatic factors for sustainable management and advancements in aquaculture practices. Environ. Sci. Pollut. Res., 31(23): 34082-34096. https://doi.org/10.1007/s11356-024-33355-1
Hossain, M.Y. and J. Ohtomi. 2010. Growth of the southern rough shrimp Trachysalambria curvirostris (Penaeidae) in Kagoshima Bay, southern. Japan J. Crustacean Biol., 30: 75-82. https://doi.org/10.1651/08-3133.1
Hossain, M.Y., M.A. Hossen, M.N.U. Pramanik, F. Nawer and M.M. Rahmanc. 2017. Life-history traits of the endangered carp Botia dario (Cyprinidae) from the Ganges River in Northwestern Bangladesh. Pak. J. Zool., 49: 801-809. https://doi.org/10.17582/journal.pjz/2017.49.3.801.809
Hossain, M.Y., M.M. Rahman, A.H. Bahkali, K. Yahya and M.S. Arefin. 2016. Temporal variations of sex ratio, length weight relationships and condition factor of Cabdio morar (Cyprinidae) in the Jamuna (Brahmaputra River distributary) River, Northern Bangladesh. Pak. J. Zool., 48: 1099-1107.
Hossain, M.Y., M.S. Arefin, M.S. Mohmud, M.I. Hossain, M.A.S. Jewel, M.M. Rahman, F. Ahamed, Z.F. Ahmed and J. Ohtomi. 2013a. Length‐ weight relationships, condition factor, gonadosomatic index‐ based size at first sexual maturity, spawning season and fecundity of Aspidoparia morar (Cyprinidae) in the Jamuna River (Brahmaputra River distributary), northern Bangladesh. J. Appl. Ichthyol., 29: 1166-1169. https://doi.org/10.1111/jai.12127
Hossain, M.Y., M.M. Rahman, E.M. Abdallah and J. Ohtomi. 2013b. Biometric relationships of the pool barb Puntius sophore (Hamilton 1822) (Cyprinidae) from three major Rivers of Bangladesh. Sains Malays., 22: 1571-1580.
Hossen, M.A., A.K. Paul, M.Y. Hossain, J. Ohtomi, W. Sabbir, O. Rahman, J. Jasmin, M.N. Khan, M.A. Islam, M.A. Rahman, D. Khatun and S. Kamaruzzaman. 2019. Estimation of biometric indices for Snakehead Channa punctata (Bloch, 1793) through Multi-model Inferences. Jordan J. Biol. Sci., 12: 197-202.
Ilah, N.E.F., S. Molla, J. Abedin, M.S. Khatun, T.A. Laboni, M.M. Rahman, W. Sabbir and M.Y. Hossain. 2024. Exploring the biological aspects of Harpodon nehereus in the Bay of Bengal, Bangladesh: Suggestions for catchable size. Aquat. Resour. Sci., 1: 36-47.
Ilah, N.E.F., M.J. Abedin, E.J. Alice, T.A. Laboni, M.S. Khatun, M.S. Sarmin, M.A. Rahman, O. Rahman, M.A. Islam, M.A.F. Siddquy and M.Y. Hossain. 2023. Growth and conditions appraisal of Atropus atropos (Carangidae) in the Bay of Bengal. Sarhad J. Agric., 39(4): 823-831. https://doi.org/10.17582/journal.sja/2023/39.4.823.831
IUCN, 2015. The IUCN red list of threatened species. Version 2015-4. http://www.iucnredlist.org/details/166588/0. Accessed on 2016-01-26.
IUCN, 2022. The IUCN red list of threatened species. Version 2022-2.
Jayaram, K.C., 1981. The freshwater fishes of the indian region. Narendera Publ. House, New Delhi. pp. 551.
Khatun M.S., M.R.K. Kabir, T.A. Laboni, M.A. Islam, M.R. Hasan, K. Gabol and M.A. Rahman. 2023. Exploring the life history traits of Polynemus paradiseus (Linnaeus, 1758) in the Bay of Bengal, Bangladesh. Fish. Stud., 1: 20-31.
Kumar, R., S.S. Yadav and M. Tripathi. 2014. Studies on length weight relationship of seven commercially important freshwater fish species of Gomti River Lucknow (U.P.) Indian Int. J. Fish. Aquat. Sci., 1(3): 1-3.
Laboni, T.A., M.S. Khatun, O. Rahman, M.S. Sarmin, Y.A. Ratry, M.M. Uddin, T.R. Likhon and K.A. Habib. 2024a. First report on population parameters of Bengal tongue sole (Cynoglossus cynoglossus): Suggestion for optimum catchable length in the Bay of Bengal, Bangladesh. Aquat. Resour. Sci., 1: 1-11.
Laboni, T.A., H. Khatun, M. Khatun, M.A. Rahman, M.A. Islam, Y.A. Ratry and M.Y. Hossain. 2024b. Reproductive performance of Channa striata in wetland ecosystems: A fuzzy logic approach to water quality and eco-climatic factors for long-term sustainable management and aquaculture advancement. Environ. Sci. Pollut. Res., 31(59): 67051-67069. https://doi.org/10.1007/s11356-024-35701-9
Le Cren, E.D., 1951. The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). J. Anim. Ecol., 20: 201–219. https://doi.org/10.2307/1540
Maurya, A.K., K.V. Radhakrishnan, P. Sahu, L. Prasad, J. Pal and B.N. Shukla. 2018. Length weight relationship and condition factor of Mystus bleekeri in Rudrasagar Lake, a Ramsar site in Tripura. J. Entomol. Zool. Stud., 6(2): 2500-2503.
Memon, N.N., F.N. Talpur and M.I. Bhanger. 2010. A comparison of proximate composition and fatty acid profile of Indus River species. Int. J. Food Prop., 13: 328–337. https://doi.org/10.1080/10942910802398479
Mishra, K.S., 1959. An aid to the identification of the common commercial fishes of India and Pakistan. Rec. Indian Mus., 57(1-4): 1-320. https://doi.org/10.26515/rzsi/v57/i1-4/1959/161986
Nath, S., 1994. Studies on the bioecology of fishes of Jammu Province (Jammu and Kashmir State) India, Part II: Feeding ecology. Recent Advances in Fish Ecology, Limnology and Eco-conservation 3: 63.
Neuman, R.M. and M.S. Allen. 2001. Analysis and interpretation of freshwater fisheries data. Department of Natural Resources Management and Engineering, University of Connecticut, USA.
Nikolsky, G.V., 1963. The ecology of fishes. Academic Press, London, pp. 1-352.
Offem, B.O., Y. Akegbejo-Samsons and I.T. Omoniyi. 2007. Biological assessment of Oreochromis niloticus (Pisces: Cichlidae: Linne, 1958) in a tropical floodplain River. Afr. J. Biotechnol., 6: 1966-1971. https://doi.org/10.5897/AJB2007.000-2300
Ranjan, J.B., W. Herwig, S. Subodh and S. Michael. 2005. Study of the length frequency distribution of sucker head, Garra gotyla gotyla (Gray, 1830) in different rivers and seasons in Nepal and its applications. Kathmandu Univ. J. Sci. Eng. Technol., 1(1): 1-14. https://doi.org/10.3126/kuset.v1i1.64288
Richter, T.J., 2007. Development and evaluation of standard weight equations for bridgelip suckers and large-scale suckers. N. Am. J. Fish. Manage., 27: 936-939. https://doi.org/10.1577/M06-087.1
Rypel, A.L. and T.J. Richter. 2008. Empirical percentile standard weight equation for the black tail red horse. N. Am. J. Fish. Manage., 28: 1843-1846. https://doi.org/10.1577/M07-193.1
Sani, R.B.K., U.K. Gupta, A. Sarkar, V.K. Pandey, Dubey and W.S. Lakra. 2016. Length-weight relationships of 14 Indian freshwater fish species from the Betwa (Yamuna River tributary) and Gomti (Ganga River tributary) Rivers. J. Appl. Ichthyol., 26: 456-459. https://doi.org/10.1111/j.1439-0426.2009.01388.x
Saraswat, D., W.S. Lakra, P. Nautiyal, M. Goswami, K. Shyamakant and A. Malakar. 2013. Genetic characterization of Clupisoma garua (Hamilton 1822) from six Indian populations using mtDNA cytochromebgene. Mitochondrial DNA, 25(1): 70–77. https://doi.org/10.3109/19401736.2013.782014
Shulman, M.J. and J.C. Ogden. 1987. What controls tropical reef-fish population: Recruitment or benthic mortality? An example in the Caribbean reef fish Haemulon flabolineatum. Mar. Ecol. Progr. Ser., 39: 233-242. https://doi.org/10.3354/meps039233
Siddik, M.A.B., M.R. Chaklader and M.A. Hanif. 2016. Variation in the life-history traits of a Schilbid catfish, Clupisoma garua (Hamilton, 1822) in the coastal waters of southern Bangladesh. Chinese J. Oceanol. Limnol., 35(5): 1189-1196. https://doi.org/10.1007/s00343-017-6008-6
Talwar, P.K. and A.G. Jhingran. 1991. Inland fishes of India and adjacent countries, Vol. II, Oxford and IBH Publishing Co. Pvt. Ltd. New Delhi-Calcutta pp. 596- 597.
Tesch, F.W., 1971. Age and growth. In: (ed. W.E. Ricker). Methods for assessment of fish production in fresh waters. Oxford, UK: Blackwell Scientific Publications pp. 99-130.
Ullah, M.R., 2022. A comprehensive impression on endangered Garua Bachcha, Clupisoma garua (Hamilton, 1822) from the habitat of Bangladesh. A review. Int. J. Zool. Anim. Biol., 5(1): 000347. https://doi.org/10.23880/IZAB-16000347
Verma, J. and M. Serajuddin. 2017. Intra-specific and inter-generic phylogenetic relationships in endangered catfish (Clupisoma garua and Eutropiichthys vacha) of family schilbeidae. J. Entomol. Zool. Stud., 5: 198-202.