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Length-Weight Relationships, Condition Factor and Morphometric Characteristics of Schizothoracinae from Neelum and Jhelum Rivers of Azad Jammu and Kashmir, Pakistan

PJZ_53_1_351-361

Length-Weight Relationships, Condition Factor and Morphometric Characteristics of Schizothoracinae from Neelum and Jhelum Rivers of Azad Jammu and Kashmir, Pakistan

Tasleem Akhtar1, 2, Ghazanfar Ali1,* and Nuzhat Shafi2

1Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad

2Department of Zoology, University of Azad Jammu and Kashmir, Muzaffarabad

ABSTRACT

The morphometrics, length-weight relationships and condition factor are presented for commercially important Schizothoracinae from Neelum and Jhelum rivers during 2015-2016. In the present study, four species of Schizothorax had been found, in which three species were already reported (S. esocinus, S. plagiostomus and S. progastus) and one new species (S. niger) was found first time in AJK. One hundred and fifty-nine specimens of S. plagiostomus, 74 specimens of S. esocinus, 21 specimens of S. progastus and 8 specimens of S. niger were taken for the study. The maximum snout length, eye diameter, length of lateral line, head length, dead depth and pre anal length were observed in S. niger followed by S. esocinus and two other species. Overall value of “b’ fluctuated from 1.183 to 2.711 which did not follow the cube law (b=3) and indicated the negative allometric (b<3) growth pattern. Studies on condition factor (K) of Schizothorax species revealed the lowest values. High pollution load and environmental stress on these species seems to be very high and not led to the ideal growth pattern. It is concluded that, the fish is under the physiological stress and it is very essential for fishery managers to impose adequate regulations for sustainable fishery management and conservation in this state of Pakistan, in which most of population depend upon fish resources. No information regarding LWRs and morphometric measurements of S. progastus and S. niger was available in Fish Base.


Article Information

Received 02 September 2018

Revised 04 March 2019

Accepted 03 May 2019

Available online 28 December 2020

Authors’ Contribution

TA and GA designed the experiments, analyzed the data and wrote the manuscript. TA conducted the experiments. NS helped in sample collection.

Key words

Co-efficient of correlation, LWR, Morphometrics, Schizothoracinae, Wellbeing of fish

DOI: https://dx.doi.org/10.17582/journal.pjz/20180216090213

* Corresponding author: ali.phd.qau@gmail.com

0030-9923/2021/0001-0351 $ 9.00/0

Copyright 2021 Zoological Society of Pakistan



INTRODUCTION

Many freshwater fish species are currently threatened by direct and indirect influence of human activities, such as habitat destruction and fragmentation (Mir et al., 2013). Construction of dams across rivers in particular affects fish movements, which may restrict the gene flow and lead to differentiation of populations (Meldgaard et al., 2003). The anthropogenic disturbances are likely to alter the genetic diversity within populations and genetic differentiation between populations (Yamamoto et al., 2004). The long-term isolation of populations and interbreeding can lead to morphometric variations between populations, and this morphometric variation can provide a basis for population differentiation. Morphometric differences among stocks of a species are recognized as an important tool for evaluating the population structure and as a basis for identifying stocks (Turan, 1999).

Morphological characters useful in identification include shape of head, position and shape of the mouth, size and number of scales and gill rakers (Jhingran, 1991). Morphological variation in fishes may provide a good record of short-term population structuring. It is often environmentally induced for aquatic environments can exhibit great spatial or temporal variability in both abiotic and biotic habitat parameters (Langerhans et al., 2003; Langerhans et al., 2007). There are many well documented studies that provide evidence for stock discrimination based on traditional morphometric characters (Quilang et al., 2007; Więcaszek et al., 2007; Bektas and Belduz, 2009). However, a new system of morphometric measurements called the truss network system, constructed with the help of landmark points, has been increasingly used for stock identification (Mir et al., 2013).

Like the other morphological characteristics, the LWR could be used for the taxonomic differentiation and different developmental events such as onset of maturity, metamorphosis and growth (Thomas et al., 2003). It can also be used to create an equation to quantify the total fish landed and compare the different population in a specific area (Singh et al., 2011). LWR is helpful in fish biology in numerous ways: to calculate the total fish weight from its length, to estimate the condition factor, life history and morphometric characters of different populations (Sani et al., 2010) and to study the allometric changes (Teixeira de Mello et al., 2006).

Moreover, the weight-length relationship improves the information about the history of commercially valuable fishes, thus enhance the knowledge of conservation and management. Fulton’s condition factor (Kn) is generally used in fisheries science to describe the condition of fish by calculating the weight-length relationship (Froese, 2006). The state of sexual maturity, age, sex, and the availability of food sources in fish species were indicated by different values in K (Anibeze, 2000). The LWR is also very essential component of Fish Base (Froese and Pauly, 2012). Additionally, it also provides useful information of environmental and climate changes, and variation in practices of human survival. A lot of LWR data is available for European and North American freshwater fishes, but are lacking for most tropical and sub-tropical fish species (Dubey et al., 2012; Mir et al., 2012).

Family Cyprinidae, genus Schizothorax locally known as snow trout is abundant in the Rivers and streams of the Himalaya and Central Asia (Mir et al., 2012). Schizothorax species are the endemic carps of Neelum and Jhelum Rivers of Azad Jammu and Kashmir, Pakistan. Genus Schizothorax in these rivers was represented by four species i.e., S. plagiostomus, S. esocinus, S. niger and S. progastus. It is highly preferred by the local masses because of its food value and taste that fetches high market price (Akhtar et al., 2016).

LWR have been extensively studied across the world (Bhat et al., 2010; Drouineau et al., 2010; Shadi et al., 2011; Dar et al., 2012; Sarkar et al., 2012; Mir et al., 2012). In Azad Jammu and Kashmir, there is inadequate study on LWRs and condition factor of snow trouts fishes a recent contribution of Akhtar et al. (2016) is available on LWR, condition factor and sex ratio of only S. plagiostomus from River Neelum and Jhelum of Kashmir. Moreover, there is no information about morphometrics, LWR and wellbeing of other Schizothorax species from River Neelum and Jhelum of AJK therefore, taking into consideration of above facts, the current study was conducted to establish the growth pattern, general condition and morphometrics of these species from natural habitat for conservation and assessment.

 

MATERIALS AND METHODS

Ethical statement

All animal experimental procedures were conducted in accordance with local and international regulations. The international regulation is the Wet op de dierproeven (Article 9) of Dutch Law (International).

Sample collection

Current study estimates the weight-length relationship, condition factor and morphometric characteristics of four endemic Schizothorax species from river Neelum and Jhelum of AJK, Pakistan during 2015 to 2016. The fish samples were randomly collected by local fisherman from River Jhelum and Neelum, Muzaffarabad (from Ghori to Kohala) with GPS coordinates viz. river Neelum (Ghori, 34°26’47.1”N 73°30’38.9”E; Challah Bandi, 34°23’03.0”N 73°27’53.8”E) and river Jhelum (Airport, 34°19’46.3”N 73°30’44.8”E; Garhi Dupatta, 34°14’05.7”N 73°36’31.6”E; Domail, 34°21’14.6”N 73°28’03.8”E; Chatter, 34°20’13.8”N 73°27’10.8”E; Ambore, 34°19’50.3”N 73°27’57.1”E; Chatter Kalass, 34°12’25.1”N 73°29’50.8”E; Kohala, 34°05’48.2”N 73°29’52.0”E) from 2014 to 2015.

The collection points in the study were not part of any reserve forests, protected area, and national park. All the fish samples were carefully handled to avoid the damages during studies. The Board of Advanced Studies and Research, University of Azad Jammu and Kashmir, Muzaffarabad permit to conduct this study in Jhelum and Neelum Rivers of Muzaffarabad city. No specific permission was required for collection sites and the collected fish samples were anesthetized by immersion in 1% benzocaine in water and euthanized by benzocaine excess. The labeled samples were packed in polyethylene bags and brought back to the Laboratory of Molecular Genetics, University of Azad Jammu and Kashmir for further research analysis. After analysis, voucher specimens were kept in 70% ethanol and stored in Zoological museum hall of the University of Azad Jammu and Kashmir, Pakistan. The collected voucher specimen were recognized according to Jayaram (1999) identification key. The S. plagiostomus has a suctorial mouth and the body is uniformaly silvery without any black spot. The dorsal fin of S. plagiostomus is inserted nearer to the tip of snout than caudle fin base. The phenotypic characters of S. progastus are similar to S. plagiostomus but, the dorsal fin is inserted midway between the tip of snout and caudle fin base. The S. niger, has a mouth horse-shoe shaped. Its lips are rounded and fleshy and the body is much darker in color. In S. esocinus, the mouth is not sectorial while, the lips are soft and pointed. The cleft of mouth is deep while, the side and back of the body have the small irregular spots. These species were also identified by Akhtar and Ali (2016) through molecular DNA barcoding, and barcode of life data system search engine (BOLD). After removing the excess water on the specimens by pressing with blotting paper, the weight and length measurements were taken at the site using measuring scale (accuracy of 0.1cm) and digital weighing balance (accuracy of 0.01g), respectively.

 

Table I. Estimated parameters of the length-weight relationships for Schizothorax species in Neelum and Jhelum Rivers of Azad Jammu and Kashmir.

Species name

Number

Length (cm)

Weight (g)

Min-Max

Mean± SD

Min-Max

Mean± SD

S. plagiostomus

159

17-39

28.35±4.83

50.5-542

245.59±103.29

S. esocinus

74

13-36

27.29±4.84

50-554

258.03±89.66

S. progastus

21

24-39

30.85±3.93

163-534

274.26±74.49

S. niger

8

23-38

29.37±4.72

175-520

257.12±113.83


 

Length-weight relationship of four fish species was examined by evaluating weight and length of fish specimens collected from River Neelum and Jhelum Muzaffarabad. The correlation between these parameters were assembled by following the equation of Froese (2006). W= a Lb Where, W= weight of fish (g), L=length of fish (cm), a= constant and b= an exponent. This equation was converted into logarithmic form gives a straight line relationship graphically. Log W= Log a + b Log L Through condition factor, the fitness and general wellbeing of fish was calculated based on the statement that heavier fish of a given length are in better condition (Mir et al., 2012). The condition factor was calculated by following Fulton (1904) equation.

K= W*100/L3 Where, W= weight (g), L= length (cm) and 100 is a factor to bring the value of K near unity. The morphometric correlation coefficient (r), regression coefficients (a and b) between TL, HL with rest of the body parameters was calculated using Graph Pad Prism for Windows (version 5.03) and also used to plot graphs.

 

Table II. The significant correlation of various morphometric parameters with TL and HL in the four Schizothorax species.

Independent

variable

Dependent

variable

P values

S. plagiostomus

S. esocinus

S. niger

S. progastus

Total length (TL)

Fork length

< 0.0001(****)

< 0.0001(****)

< 0.0001(****)

< 0.0001(****)

Standard length

< 0.0001(****)

< 0.0001(****)

< 0.0001(****)

< 0.0001(****)

Head length

< 0.0001(****)

0.2187(ns)

0.6578(ns)

0.1732(ns)

Max. body depth

< 0.0001(****)

0.4353(ns)

0.8952(ns)

0.5616(ns)

Pre dorsal length

< 0.0001(****)

0.0917(ns)

0.7582(ns)

0.7381(ns)

Pre pectoral length

< 0.0001(****)

0.0049(**)

0.8971(ns)

0.7230(ns)

Pre pelvic length

< 0.0001(****)

0.0010(**)

0.8269(ns)

0.5613(ns)

Pre anal length

< 0.0001(****)

< 0.0001(****)

0.7758(ns)

0.6346(ns)

Snout length

0.8823(ns)

0.6914(ns)

0.2185(ns)

0.0121(*)

Eye diameter

0.4952(ns)

0.3067(ns)

0.5589(ns)

0.6224(ns)

Length of lateral line

< 0.0001(****)

< 0.0001(****)

0.7048(ns)

0.6606(ns)

Head depth

< 0.0001(****)

0.5774(ns)

0.5264(ns)

0.3295(ns)

Head length (HL)

Fork length

< 0.0001(****)

0.2671(ns)

0.6565(ns)

0.1574(ns)

Standard length

< 0.0001(****)

0.2671(ns)

0.5800(ns)

0.1574(ns)

Max. body depth

< 0.0001(****)

0.2671(ns)

0.0185(*)

0.1942(ns)

Pre dorsal length

< 0.0001(****)

0.2671(ns)

0.2085(ns)

0.0743(ns)

Pre pectoral length

0.0474(*)

0.2671(ns)

0.2938(ns)

0.5264(ns)

Pre pelvic length

0.0416(*)

0.2671(ns)

0.3485(ns)

0.4003(ns)

Pre anal length

< 0.0001(****)

0.2671(ns)

0.3011(ns)

0.1217(ns)

Snout length

0.0002(***)

0.2671(ns)

0.8374(ns)

0.4800(ns)

Eye diameter

0.1035 (ns)

0.2671(ns)

0.9457(ns)

0.9999(ns)

Length of lateral line

< 0.0001(****)

0.2671(ns)

0.2805(ns)

0.0167(*)

Head depth

< 0.0001(****)

0.2671(ns)

0.0240(*)

0.0086(**)

 

Significant (alpha = 0.05); ns: non-significant.

 

RESULTS

Overall, 262 length-weight relationships, condition factor and morphometric characteristics referring to four Schizothorax fish species from rivers of Azad Jammu and Kashmir, Muzaffarabad. S. plagiostomus was the most dominant fish in the Rivers Neelum and Jhelum, followed by S. esocinus and S. progastus while, we received the low catch of the S. niger from the study area during our whole collection.

A total of 159 specimens of S. plagiostomus were collected randomly from these rivers which ranged in total length from 17 to 39 cm and in total weight from 50.5 to 542 g (Table I). The total length was 1.08 times the fork length, 1.18 times the standard length, 2.19 times the pre-dorsal length, 1.55 times the pre-anal length, 2.99 times the pre-pectoral length, 2.15 times the pre-pelvic length, 1.52 times the length of lateral line, 5.22 times the total body depth, 6.80 times the head length, 7.31 times the head depth, 14.83 times the eye diameter and 15.44 times the snout length. All these parameters recorded significant positive relationship (P < 0.001) with the total length except the eye diameter and snout length. These two parameters show non-significant relationship with the total length (Table II; Fig. 1A).

The head length was 0.15 times the fork length, 0.17 times the standard length, 0.32 times the pre-dorsal length, 0.22 times the pre-anal length, 0.43 times the pre-pectoral length, 0.31 times the pre-pelvic length, 0.22 times the length of lateral line, 0.76 times the total body depth, 1.07 times the head depth, 2.17 times the eye diameter and 2.27 times the snout length. All these parameters recorded significant positive relationship with the head length while, the eye diameter show non-significant relationship with

 

Table III. Correlation coefficient (r) and regression coefficients (a & b) of various morphometric parameters with TL and HL in the four Schizothorax spp.

Indep-endent variable

Depen-dent variable

S. plagiostomus

S. esocinus

S. niger

S. progastus

a

b

r

a

b

r

a

b

r

a

b

r

Total length (TL)

Fork length

-1.86

0.987

0.994

-1.277

0.965

0.994

-1.151

0.972

0.996

-1.603

0.982

0.995

Standard length

-3.59

0.972

0.989

-3.062

0.960

0.993

-3.39

0.972

0.994

-3.603

0.982

0.994

Head length

2.58

0.056

0.350

3.446

0.021

0.144

5.240

0.031

0.186

2.171

0.064

0.333

Max. body depth

1.23

0.148

0.387

4.635

0.033

0.092

7.255

0.023

0.056

6.273

0.061

0.148

Pre dorsal length

4.30

0.305

0.510

10.20

0.110

0.197

11.82

0.065

0.130

12.27

0.049

0.073

Pre pectoral length

-0.359

0.347

0.401

2.211

0.275

0.323

9.210

0.047

0.054

9.376

0.077

0.072

Pre pelvic length

3.34

0.346

0.394

4.312

0.309

0.373

13.73

0.088

0.092

14.88

0.139

0.135

Pre anal length

5.38

0.455

0.594

7.496

0.380

0.502

18.33

0.073

0.120

13.49

0.101

0.095

Snout length

1.88

-0.001

0.011

1.647

0.006

0.120

4.574

0.066

0.048

3.206

0.045

0.532

Eye diameter

1.67

0.008

0.053

1.367

0.021

0.046

4.388

0.059

0.244

1.433

0.016

0.138

Length of lateral line

3.48

0.531

0.645

8.716

0.352

0.448

18.99

0.099

0.160

12.73

0.122

0.106

Head depth

2.21

0.400

0.340

3.593

0.011

0.065

1.992

0.074

0.264

5.371

0.057

0.263

Head length (HL)

Fork length

17.62

2.041

0.327

21.56

0.873

0.130

32.11

0.084

0.187

21.93

1.629

0.319

Standard length

15.79

1.964

0.318

19.30

0.959

0.144

31.13

0.350

0.232

19.93

1.629

0.318

Max. body depth

-0.124

1.332

0.554

5.793

0.057

0.022

-1.972

1.979

0.794

7.000

0.628

0.295

Pre dorsal length

6.321

1.585

0.424

13.88

0.167

0.043

7.357

1.483

0.498

16.48

1.379

0.397

Pre pectoral length

5.905

0.853

0.157

10.16

0.106

0.018

-1.566

2.175

0.425

10.34

0.807

0.146

Pre pelvic length

9.441

0.887

0.161

13.25

0.121

0.021

1.776

2.168

0.383

14.86

1.029

0.193

Pre anal length

10.01

1.979

0.413

15.10

0.688

0.137

13.99

1.510

0.419

24.54

1.900

0.348

Snout length

0.841

0.238

0.289

2.033

0.048

0.047

2.927

0.069

0.873

2.107

0.071

0.163

Eye diameter

1.373

0.129

0.129

1.826

0.029

0.024

2.444

0.041

0.280

1.929

0.091

0.012

Length of lateral line

10.31

1.972

0.382

18.43

0.021

0.003

14.19

1.608

0.435

29.32

0.071

0.515

Head depth

2.210

0.399

0.339

4.100

0.044

0.035

-1.392

1.294

0.774

6.214

0.628

0.557

 

the head length (Table III) (Fig. 1B). The length-weight relationship in the fish was represented by the equation; Log W = -3.08 + 1.301 Log L (Fig. 1C)

The condition factor (Kn) of S. plagiostomus was also calculated as 0.87 in current study. Seventy four specimens of S. esocinus having total length from 13 to 36 cm and total weight from 50 to 454.5 g were collected during current study. The total length was 1.09 times the fork length, 1.19 times the standard length, 2.06 times the pre-dorsal length, 1.52 times the pre-anal length, 2.8 times the pre-pectoral length, 2.13 times the pre-pelvic length, 1.48 times the length of lateral line, 4.71 times the total body depth, 6.78 times the head length, 8.39 times the head depth, 14.06 times the eye diameter and 14.9 times the snout length. Fork length, standard length, pre pectoral length, pre pelvic length, pre anal length and length of lateral line show the significant positive relationship while, the rest of parameters show the non-significant relationship with total length (Fig. 2A).

Head length was 0.16 times the fork length, 0.17 times the standard length, 0.30 times the pre-dorsal length, 0.22 times the pre-anal length, 0.41 times the pre-pectoral length, 0.31 times the pre-pelvic length, 0.21 times the length of lateral line, 0.79 times the total body depth, 1.23 times the head depth, 2.05 times the eye diameter and 2.19 times the snout length. All these parameters recorded non-significant relationship with the head length (Fig. 2B). The length-weight relationship in S. esocinus was represented by the equation

Log W = -1.661+1.183 Log L (Fig. 2C). While, condition factor (Kn) of S. esocinus was 0.839

S. progastus was represented by 21 specimens which ranged in length from 24–39 cm and in weight from 163 to 534 g. Statistical analysis of the data revealed that the total length was 1.07 times the fork length, 1.15 times the standard length, 2.87 times the pre-dorsal length, 1.85 times the pre-anal length, 2.42 times the pre-pectoral length, 2.91 times the pre-pelvic length, 1.86 times the length of lateral line, 4.07 times the total body depth, 7.40 times the head length, 8.59 times the head depth, 16.60 times the eye diameter and 16.23 times the snout length. Fork length, standard length, and snout length show the significant positive relationship while, the rest of all the parameters show the non-significant relationship with total length (Fig. 3A).

Similarly, head length was 0.14 times the fork length, 0.15 times the standard length, 0.38 times the pre-dorsal length, 0.25 times the pre-anal length, 0.59 times the pre-pectoral length, 0.39 times the pre-pelvic length, 0.25 times the length of lateral line, 0.95 times the total body depth, 1.16 times the head depth, 2.16 times the eye diameter and 2.19 times the snout length. The length of lateral line and head depth show the significant positive relationship while, rest of all the parameters show the non-significant relationship with head length. (Fig. 3B). The length-weight relationship in S. progastus was represented by the equation Log W = -2.081+2.50 Log L (Fig. 3C). The condition factor of S. progastus was 0.826.

Eight specimens of S. niger having total length from 23 to 38 cm and total weight from 175 to 520 g were collected during current study. The total length of S. niger was 1.07 times the fork length, 1.16 times the standard length, 2.13 times the pre-dorsal length, 1.43 times the pre-anal length, 3.76 times the pre-pectoral length, 2.64 times the pre-pelvic length, 1.39 times the length of lateral line, 4.47 times the total body depth, 7.02 times the head depth, 11.10 times the eye diameter and 11.20 times the snout length. Fork length and standard length show the significant positive correlation while, the rest of all the variables show the non-significant relationship with total length (Fig. 4A).

Head length was 0.15 times the fork length, 0.17 times the standard length, 0.31 times the pre-dorsal length, 0.21 times the pre-anal length, 0.55 times the pre-pectoral length, 0.38 times the pre-pelvic length, 0.20 times the length of lateral line, 0.65 times the total body depth, 1.03 times the head depth, 1.64 times the eye diameter and 1.63 times the snout length. Head length show the significant relationship with body depth and head depth while, rest of all the parameters show the non-significant correlation with head length (Table II; Fig. 4B). The length-weight relationship in S. niger was represented by the equation Log W = -3.51+2.711 Log L (Fig. 4C) and the condition factor of S. niger was 0.859. S. plagiostomus and S. esocinus shows that weight of fish is not growing in accordance with the length of fish and significantly deviate from the isometric growth (b=3).

 

DISCUSSION

The morphometric measurements have been widely used for fish identification (Yousuf et al., 2003). S. progastus showed the shortest head length, body depth, head depth, snout length, eye diameter and pre pectoral length as compared to other three species. The maximum snout length, eye diameter, length of lateral line, head length, dead depth and pre anal length were observed in S. niger followed by S. esocinus and two others. Bhat et al. (2010) also reported the similar type of study and concluded that S. esocinus showed maximum growth in head length, pre-dorsal length, pre-pectoral length and eye diameter, while S. plagiostomus ranked second in pre-dorsal length while, maximum caudal fin length and pre-anal length was observed in S. plagiostomus.

The variations in various morphometric parameters of these species were statistically significant and thus can be regarded as different species (Yousuf et al., 2001; Bhat et al., 2010). Values of b for S. progastus and S. niger were within the normal range of 2.5–3.5, as suggested by Froese (2006), while the S. plagiostomus and S. esocinus showed the negative allometric growth pattern which indicates that, these fish species are not growing in accordance with the increase in their total length. The divergences between expected and calculated values may be due to habitat, low number of specimens examined, size range covered, seasonal variation, extent of stomach fullness, sex, sexual maturity, and the health condition of fishes (Froese, 2006; Jamali et al., 2014; Khan and Sabah, 2013), lack of covering all size-classes, or over-representing juveniles that were not considered in the present study.

Previous findings on the WLR of cyprinid fishes revealed that, most of them rigorously follow the cue law (b=3) while, the other showed the positive allometry (b>3) or negative allometry (b<3). Qadri and Mir (1980) reported the value of “b” as 2.448 for S. plagiostomus from the peripheral water bodies of Dal Lake, while Bhagat and Sunder (1983) reported it to be 2.928 for the same fish from the Jammu water bodies. Similarly, from Lidder Lake, the value of “b” for this fish was calculated as 2.9467 (Bhat et al., 2010); however, Khan and Sabah (2013) reported the “b” value of same fish as 2.86 from Kashmir valley while, Akhtar et al. (2016) recorded the value of same fish as 1.672 from Neelum and Jhelum rivers, Azad Kashmir. The previous findings of Akhtar et al. (2016) verify the present findings on the value of “b” as 1.301 for S. plagiostomus. S. plagiostomus also shows that, the weight of fish is not growing in accordance with the length of fish and significantly deviate from the isometric growth.

Isometric growth pattern has been reported in case of S. esocinus “b” as 3.0180 from the Dal Lake


 

 

 

(Bhagat and Sunder, 1983), while, Bhat et al. (2010) reported it to be 3.00 from River Lidder of Kashmir. However, Khan and Sabah (2013) recorded the value in the same fish as 3.08 from Kashmir valley, while, Dar et al. (2012) reported it to be 2.86 from river Jhelum Kashmir and Mir et al. (2014) reported the value of this fish as 2.98 from Kashmir valley India. In S. esocinus, the value of “b” in the present study was found as 1.183 which, show the deviation from isometric growth pattern.

The value of “b” of S. progastus was calculated as 2.442 in current study. No previous findings were reported for the “b” value of S. progastus. Shafi and Yousuf (2012) observed that the value of “b” as 3.07 in S. niger from Dal lake, while, Khan and Sabah (2013) reported the value of “b” of same fish as 2.66 from Kashmir valley. However, the value of “b” of same fish was observed as 2.711 in current study.

The value of b calculated from present study is different from the previous findings, which is possibly due to several factors such as the habitat, number of specimens examined and length ranges and length types used. Among these fishes S. esocinus and S. plagiostomus deviated more from the value of “b” as compared to S. niger and S. progastus. As suggested by Petrakis and Stergiou (1995), use of LWRs should be strictly limited to the observed length ranges applied in the estimation of the linear regression parameters. Study of WLR has the great importance in fisheries conservation and its management, as it supports to understand the general wellbeing and growth patterns (isometric and allometric) of fish population and is influenced by many environmental factors like pH, temperature, salinity, dissolved oxygen, ammonia and heavy metal concentration. Yousuf and Firdous (1992) and Yousuf et al. (2001) observed that environmental factors are responsible for the deviation from the ideal state to a great extent. All the fish species under Schizothoracinae, reported in the Rivers of Azad Kashmir during the present study are typical inhabitants of running habitats in their distributional range. It can be determined that in Schizothorax species gain weight at slower rate in relation to its length.

Le Cren (1951) reported that the condition factor higher than one directed to the good health of fish whereas, its value lower than one indicated that fish is not healthy. The current study revealed that all the species were found to be not in good condition and recorded a “Kn” value lesser than one which ranged from 0.826 to 0.874. A change in Kn value of different fish species were due to change in their spawning cycle (Narejo et al., 2002; Mir et al., 2012), feeding rhythms or change in environmental factors (Doddamani and Shanbouge, 2001) and also by pollution (Devi et al., 2008). According to Jan and Ahmed (2016) and Dar et al. (2012), the fluctuations in condition factor in Schizothorax species could be credited to the reproductive cycles and food concentration. The result of this study shows negative allometric growth pattern and it is a bit difficult to say that, environment is supportive of the growth, reproduction and survival of Schizothorax species. Current findings provide the baseline and useful information about morphometrics, weight-length relationship and general health of four commercially important Schizothorax species of river Neelum and Jhelum Muzaffarabad AJK. This study could be valuable to enforce suitable systems for sustainability of fish conservation and management of these selected rivers as well as for other rivers of the Azad Jammu and Kashmir Pakistan, to prevent their complete extinction. This study also provide valuable information for the online Fish Base database as well as contribute to fishery research and its management in wild condition.

 

ACKNOWLEDGEMENTS

The author sincerely acknowledges to Raja Mubarak Ali for helping sample collection.

 

Novelty statement

In current study, one new species (Schizothorax niger) was found first time in AJK, Pakistan. This is the first study regarding length weigh relationship and morphometric measurements of S. progastus and S. niger because, no information is available for these species in Fish Base.

 

Statement of conflict of interest

The authors declare there is no conflict of interest.

 

REFERENCES

Akhtar, T., Shafi, N. and Ali, G., 2016. Length-weight relationship, condition factor and sexratio of snow trout (Schizothorax plagiostomus) from Neelum and Jhelum rivers, Muzaffarabad, Azad Kashmir. Int. J. Fish aquat. Stud., 4: 513-517.

Akhtar, T. and Ali, G., 2016. DNA bar-coding of Schizothorax species from Neelum and Jhelum Rivers of Azad Jammu and Kashmir. Mitochondrial DNA Part B., 1: 934–936. https://doi.org/10.1080/23802359.2016.1258337

Anibeze, C.I.P., 2000. Length-weight relationship and relative condition of Heterobranchus longifilis (Valencienness) from Idodo River, Nigeria. Naga, ICLARM Quart., 23: 34-35.

Bektas, Y. and Belduz, A.O., 2009. Morphological variation among Atlantic horse mackerel, Trachurus trachurus populations from Turkish coastal waters. J. Anim. Vet. Adv., 8: 511–517.

Bhagat, M.J. and Sunder, S., 1983. A preliminary note on the length-weight relationship and relative condition factor of Schizothorax plagiostomus (Heckel) from Jammu region. J. Inland Fish. Soc. Ind., 15: 73-74.

Bhat, F.A., Yousuf, A.R., Balkhi, M.H., Mahdi, M.D. and Shah, F.A., 2010. Length-weight relationship and morphometric characteristics of Schizothorax spp. in the River Lidder of Kashmir. Indian J. Fish., 57: 73–76.

Dar, S.A., Najar, A.M., Balkhi, M.H., Rather, M.A. and Sharma, R., 2012. Length weight relationship and relative condition factor of Schizopyge esocinus (Heckel, 1838) from Jhelum River, Kashmir. Int. J. aquat. Sci., 3: 29-36.

Devi, J.O., Nagesh, T.S., Das, S.K. and Mandal, B., 2008. Length-weight relationship and relative condition factor of Pampus argenteus (Euphrasen) from Kakdwipesturine region of West Bengal. J. Inland Fish. Soc. Ind., 40: 70-73.

Doddamani, M.T.J.R. and Shanbhogue, S.L., 2001. Length-weight relationship and condition factor of Stolephorus bataviensis from Mangalore area. Ind. J. Fish., 48: 329-332.

Drouineau, H., Mahe, S., Bertignac, M. and Duplisea, D., 2010. A length-structured spatially explicit model for estimating hake growth and migration rates. ICES. J. mar. Sci., 67: 1697–1709. https://doi.org/10.1093/icesjms/fsq042

Dubey, V.K., Sarkar, U.K., Kumar, R.S., Mir, J.I., Pandey, A. and Lakra, W.S., 2012. Length–weight relationships (LWRs) of 12 Indian freshwater fish species from an un-impacted tropical river of Central India (River Ken). J. appl. Ichthyol., 28: 854-856. https://doi.org/10.1111/j.1439-0426.2012.02005.x

Froese, R., 2006. Cube law, condition factor and weight–length relationships: history, meta-analysis and recommendations. J. appl. Ichthyol., 22: 241–253. https://doi.org/10.1111/j.1439-0426.2006.00805.x

Froese, R. and Pauly, D., 2012. Fish Base World wide web electronic publication, http://www.fishbase.org, version 4.

Fulton, T.W., 1904. The rate of growth of fishes. Twenty-second Annual Report Part III. Fisheries Board of Scotland, Edinburgh, pp. 141-241.

Jamali, H., Patimar, R., Farhadi, M., Golzarianpour, K. and Daraei, V., 2014. Some aspects of the life history of Turcinoemacheilus hafezi (Teleostei: Nemacheilidae) from Beshar River, southwestern Iran. Iran. J. Ichthyol., 1: 32–38.

Jan, M. and Ahmed, I., 2016. Length weight relationship and condition factor of snow trout, Schizothorax plagiostomus (Heckel, 1838) from Lidder River, Kashmir. Int. J. Fish. aquat. Stud., 4:131-136.

Jhingran, V., 1991. Culture of air-breathing fishes and non-air-breathing predatory carnivorous fishes. Fish and Fisheries of India, 3rd Ed. Hindustan Publishing Corporation, Delhi, India, 498-503.

Jayaram, K.C., 1999. The freshwater fishes of the Indian Region. Narendra Publishing House, Delhi-6, pp. 551.

Khan, M.A. and Sabah, 2013. Length–weight and length–length relationships for five fish species from Kashmir Valley. J. appl. Ichthyol., 29: 283–284. https://doi.org/10.1111/j.1439-0426.2012.02061.x

Langerhans, R.B., Layman, C.A., Langerhans, A.K. and Dewitt, T.J., 2003. Habitat-associated morphological divergence in two Neotropical fish species. Biol. J. Linn. Soc., 80: 689–698. https://doi.org/10.1111/j.1095-8312.2003.00266.x

Langerhans, R.B., Chapman, L.J. and Dewitt, T.J., 2007. Complex phenotype-environment associations revealed in an East African cyprinid. J. Evol. Biol., 20: 1171–1181. https://doi.org/10.1111/j.1420-9101.2007.01282.x

Le Cren, E.D., 1951. The Length–weight relationship and seasonal cycle in gonad weight and condition in the perch (Percafluviatilis). J. Anim. Ecol., 28: 201–219. https://doi.org/10.2307/1540

Meldgaard, T., Nielsen, E.E. and Loeschcke, V., 2003. Fragmentation by weirs in a riverine system: A study of genetic variation in time and space among populations of European grayling (Thymallus thymallus) in a Danish river system. Conserv. Genet., 4: 735–747. https://doi.org/10.1023/B:COGE.0000006115.14106.de

Mir, J.I., Sarkar, U.K., Dwivedi, A.K., Gusain,O.P. and Jena, J.K., 2013. Stock structure analysis of Labeo rohita (Hamilton, 1822) across the Ganga basin (India) using a truss network system. J. appl. Ichthyol., 29: 1097–1103. https://doi.org/10.1111/jai.12141

Mir, J.I., Sarkar, U.K., Dwivedi, A.K., Gusain, O.P., Pal, A. and Jena, J.K., 2012. Pattern of intra-basin variation in condition factor, relative condition factor and form factor of an Indian Major Carp, Labeo rohita (Hamilton-Buchanan, 1822) in the Ganges Basin, India. Eur. J. biol. Sci., 4: 126-135.

Mir, F.A., Mir, J.I., Patiyal, R.S. and Kumar, P., 2014. Length-weight relationships of four snowtrout species from the Kashmir Valley in India. J. appl. Ichthyol., 30: 1103–1104. https://doi.org/10.1111/jai.12482

Narejo, N.T., Rahmatullah, S.M. and Mamnur, M., 2002. Length-weight relationship and relative condition factor (Kn) of Monopterus cuchia (Hamilton). Indian J. Fish., 8: 54-59.

Petrakis, G. and Stergiou, K.I., 1995. Weight-length relationships for 33 fish species in Greek waters. Fish. Res., 21: 465–469. https://doi.org/10.1016/0165-7836(94)00294-7

Qadri, M.Y. and Mir, S., 1980. Length-weight relationship of Orienus plagiostomus (McCl). Geobios, 7: 158-159.

Quilang, J.P., Basiao, Z.U., Pagulayan, R.C., Roderos, R.R. and Barrios, E.B., 2007. Meristic and morphometric variation in the silver perch, Leiopotherapon plumbeus (Kner, 1864), from three lakes in the Philippines. J. appl. Ichthyol., 23: 561–567. https://doi.org/10.1111/j.1439-0426.2007.00862.x

Sani, R., Gupta, B.K., Sarkar, U.K., Pandey, A., Dubey, V.K. and Lakra, W.S., 2010. Length weight relationship of 14 Indian freshwater species from river Betwa (Yamuna River tributary) and Gomti (Ganga River tributary). J. appl. Ichthyol., 26: 456-459. https://doi.org/10.1111/j.1439-0426.2009.01388.x

Sarkar, U.K., Khan, G.E., Dabas, A., Pathak, A.K., Mir, J.I., Rebello, S.C., Pal, A. and Singh, S.P., 2012. Length weight relationship and condition factor of selected freshwater fish species found in River Ganga, Gomti and Rapti, India. J. environ. Biol., 34: 951-956.

Shadi, A., Mediseh, S.D., Kouchanian, P. and Gandomi, Y., 2011. Length-weight relationships for 6 fish species from Khuzestan (North of Persian Gulf), Iran. World J. Fish. mar. Sci., 3: 129-131.

Shafi, S. and Yousuf, A.R., 2012. Length-weight relationship and condition factor of Schizothorax niger (Heckel, 1838) Misra from Dal lake, Kashmir. Int. J. Sci. Res. Publ., 2: 1-3.

Singh, N.O., Sarma, D. and Singh, N.G., 2011. Length-weight relationship of Tor putitora (Hamilton) from Kosi River Uttarakhand considering different stages of its lifespan. Indian J. Fish., 58: 35-38.

Teixeira de Mello, F., Iglesias, C., Borthagaray, A.I., Mazzco, N., Vilches, J., Larrea, D. and Ballabio, R., 2006. Onthogenic allometric coefficient changes. Implications of diet shift and morphometric attributes in Hopliasmalabaricus (Bloch) (Characiforme, Erythrinidae). J. Fish. Biol., 69: 1770-1778. https://doi.org/10.1111/j.1095-8649.2006.01245.x

Thomas, J.S., Venus and Kurup, B.M., 2003. Length-weight relationship of some deep-sea fish inhabiting continental slope beyond 250 m depth along West coast of India Naga, NAGA. World. Fish. Center Quart., 26: 17-21.

Turan, C., 1999. A note on the examination of morphometric differentiation among fish populations: the truss system. Turk. J. Zool., 23: 259–263.

Więcaszek, B., Krzykawski, S. and Antoszek, A., 2007. Meristic and morphometric characters of small sandeel, Ammodytes tobianus L. (Actinopterygii: Ammodytidae), from the Gulf of Gdańsk, Baltic Sea. Acta Ichthyol. Piscat., 37: 37–45. https://doi.org/10.3750/AIP2007.37.1.06

Yamamoto, S., Morita, K., Koizumi, I. and Maekawa, K., 2004. Genetic differentiation of white-spotted charr (Salvelinus leucomaenis) populations after habitat fragmentation: spatial–temporal changes in gene frequencies. Conserv. Genet., 5: 529–538. https://doi.org/10.1023/B:COGE.0000041029.38961.a0

Yousuf, A.R., Firdous, G., 1992. Studies on length-weight relationship in some cyprinid fish in Manasbal Lake, Kashmir. In: Current trends in fish and fishery biology and aquatic ecology (eds. A.R. Yousuf, M.K. Raina and M.Y. Qadri). University of Kashmir, Srinagar, pp. 185 - 189.

Yousuf, A.R., Firdous, G. and Pandit, A.K., 2001. Length weight relationship in Schizothorax niger,Heckel, an endemic lacustrine fish of Kashmir. J. Res. Develop., 1: 54 -59.

Yousuf, A.R., Bhat, F.A., Mahdi, D., Ali, S. and Ahangar, M.A., 2003. Food and feeding habits of Glyptosternon reticulatum (McClelland) and Griffth in torrential streams of Kashmir Himalayas. J. Res. Develop., 3: 124 – 133.

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