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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 6 Issue 3, March-April 2022 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 19
Study on Sex Ratio and Gonadosomatic Index of
Fresh Water Fish C. Gachua (Ham.1822)
Navjyoti Ranjan Verma
Research Scholar, PG Department of Zoology, Tilka Manjhi Bhagalpur University, Bhagalpur, Bihar, India
ABSTRACT
Aspect of reproductive biology of fresh water murrel C. gachua, such
as sex ratio and Gonadosomatic Index were investigated from the
pools ,ditches and even from river Ganga in and around the area of
Bhagalpur, Bihar for a complete year span. On the basis of the
monthly variation, the overall sex ratio was recorded 1:1.22(M:F).
The spawning season extends from June to August. Gonadosomatic
Index in female fish reaches maximum in May with 44.50 %. The
GSI recorded minimum in September with 5.71% followed by Oct
with 7.21 %.GSI in male C. gachua was also studied and found the
maximum in the month of June with 4.86%, closely followed by the
month of July with 4.06%. The GSI was found the minimum in the
month of January with 0.57% closely followed by the month of
February with 0.84%.
KEYWORDS: GSI, Spawning, Sex ratio
How to cite this paper: Navjyoti Ranjan
Verma "Study on Sex Ratio and
Gonadosomatic Index of Fresh Water
Fish C. Gachua (Ham.1822)" Published
in International
Journal of Trend in
Scientific Research
and Development
(ijtsrd), ISSN: 2456-
6470, Volume-6 |
Issue-3, April 2022,
pp.19-22, URL:
www.ijtsrd.com/papers/ijtsrd49449.pdf
Copyright © 2022 by author(s) and
International Journal of Trend in
Scientific Research and Development
Journal. This is an
Open Access article
distributed under the
terms of the Creative Commons
Attribution License (CC BY 4.0)
(http://creativecommons.org/licenses/by/4.0)
INTRODUCTION
The reproductive biology of fish is greatly influenced
by season. As fishes are seasonal breeder, the season
affects its different reproductive aspects like sex ratio,
GSI and even condition factor. With the approaching
spawning all the reproductive aspects become
maximum. The Gonadosomatic index of the fish
increases with the maturation of fish, being maximum
during the peak period of maturity and declining
abruptly after spawning. The monthly studies were
made to go through the GSI of C. gachua in detail.
The spawning takes place between June to August
every year.
The sex ratio was also recorded for the complete year
period. The findings clearly shows that the ratio of
male and female fishes show an increment during the
spawning season. Sex ratio also decreases after the
spawning period ends, although it is very marginal.
Nazir et. al. 1978 in Barbusleutus; Sindhe et. al. 2004
in Notopterus notopterusand many others have
studied the same on various fishes. However no such
studies were made on C. gachua, so this studiy is
aimed on this dwarf snake headed murrel C. gachua.
MATERIALS AND METHODS
From the surrounding areas of Bhagalpur i.e. Bhairwa
pond of T M Bhagalpur University campus, river
Ganga, different pools and ditches, the dwarf snake
headed C. gachua was collected monthly and brought
to the laboratory. Studies were made on the fish to go
through its GSI, sex ratio. Each of the fish was
studied thoroughly before and after the dissection
(removing its gonads) to go through its different
reproductive aspects i.e. sex ratio and GSI. The
present study is based on the sample brought to the
laboratory. The sexes were counted and the ratio were
calculated for all the seasons.
Specimen were collected and measured for total
length (cm/mm), total weight (gm), gonads wt. and
length. Afterward the specimen were anesthetized,
dissected and preserved in 10%formalin for further
anatomical studies.
Sex ratio: The sex and maturation stage of each
specimen was determined nanoscopically considering
coloration, transparency, superficial vascularization
and for gonads the visualization and appearance of
the ova and testis.
IJTSRD49449
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 20
The maturity stages of the male and female gonads
were classified according to Biswas(1993) and
computed monthly to ascertain the breeding season.
The overall frequencies of the stages were also
estimated. Spawning season was observed between
June to August every year.
GONADOSOMATIC INDEX (GSI)
The GSI was calculated according to Vazzolar(1996):
GSI= wt. of gonad/ total body weight ×100, was
plotted monthly to identify the spawning.
After calculating the GSI %, the period of maturity of
fish was divided into four stages (Quyyam and
Quasim, 1961) Ophiocephalus punctatus.
1. Pre spawning phase
2. Spawning phase
3. Post spawning phase
4. Preparatory phase
It was observed that the Gonadosomatic index of fish
increases during peak period of maturity and it
declines abruptly post spawning.
RESULT AND DISCUSSION
SEX RATIO was studied in the laboratory. A total of 409 specimen of fishes were brought to laboratory for the
study of gonads to find out the sex ratio (F: M) The superficial vascularization was made for the visualization
and appearance of the gonads i.e. ovary and testis. The findings were collected in the form of Tab (A).
Theaverage of the findings shows the ratio of 1. 22: 1(F: M) following chi-square method (X2
).
Tab (A) Sex ratio in C. gachua.
Month Total no. of samples No. of Female % Female No. of Male % male
Sex ratio
(F: M)
January 35 19 54. 29 16 45. 71 1. 18: 1
February 32 18 56. 25 14 43. 75 1. 28: 1
March 24 12 50. 50 12 50. 00 1. 00: 1
April 40 22 55. 00 18 45. 00 1. 22: 1
May 37 20 54. 06 17 45. 94 1. 17: 1
June 33 18 54. 55 15 45. 45 1. 20: 1
July 30 18 60. 00 12 40. 00 1. 50: 1
August 34 20 58. 83 14 41. 17 1. 42: 1
September 39 21 53. 85 18 46. 15 1. 16: 1
October 34 19 55. 89 15 44. 11 1. 26: 1
November 41 22 53. 66 19 46. 34 1. 15: 1
December 30 16 53. 34 14 46. 66 1. 14: 1
Total/Avg 409 225 55. 01 184 44. 99 1. 22: 1
GSI of C. gachua was estimated for females.
Tab (B-1) shows the value of GSI (%) in females. GSI
value rises from 13. 27 % in April to 20. 43% in June. It shows the pre spawning period. The GSI gradually
decreases from 20. 43% in June to 15. 83 % in August. It means it is the spawning period. Furtheran abrupt
decrease was observed from 12. 04% in September to 9. 55% in December. This phase can be said as post
spawning phase. GSI in the month of January was calculated 5. 69% and is increased up to 11. 26 % in March
indicating the preparatory period. GSI in male was observed the maximum in the month of maximum in the
month of June with 4. 86%, closely followed by the month of July with 4. 06%. The GSI was found the
minimum in the month of January with 0. 57% closely followed by the month of February with 0. 84%.
From the above findings we observed that in C. gachua the peak value of the GSI is found only once in a year
i.e. in the month of June, which clearly indicates only one spawning period in C. gachua i.e. from June to
August.
Similar observations were found by Nazir et al1978 in Barbus luetus; Brewer et al. 2008; Sindhe e. t al. 2004 in
Notopterus notopterus; Brewer, 2008 in small riverine fishes, Mechalin Musri Musman, 2010 in Rasbora
towarensis
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 21
Tab. (B-1) GSI of female Channa gachua.
Month Avg. Body wt. (gm) Avg Ovary wt. (gm) GSI %
Sep 41. 5 5. 0 12. 04
Oct 38. 8 4. 1 10. 56
Nov 33. 0 3. 4 10. 30
Dec 31. 4 3. 0 9. 55
Jan 35. 1 2. 0 5. 69
Feb 35. 6 3. 1 8. 70
March 36. 4 4. 1 11. 26
April 36. 9 4. 9 13. 27
May 39. 0 7. 4 18. 97
June 46. 5 9. 5 20. 43
July 57. 4 11. 6 20. 20
August 44. 2 7. 0 15. 83
Chart (I) shows GSI % in Female C, gachua
Table (B-2) GSI of male C. gachua
Month Avg wt. of Fish(gm) Avg wt. of testis(gm) GSI %
Jan 35. 0 0. 2 0. 57
Feb 35. 6 0. 3 0. 84
March 36. 2 0. 4 1. 10
April 37. 0 0. 7 1. 89
May 38. 0 1. 0 2. 63
June 43. 2 2. 1 4. 46
July 50. 6 2. 3 4. 06
August 42. 4 1. 0 2. 35
Sep 38. 5 0, 5 1. 29
Oct 35. 6 0. 7 1. 96
Nov 34. 2 0. 3 0. 87
Dec 32. 8 0. 2 0. 60
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 22
Chart (II) showing GSI % in male C. gachua.
LITERATURE CITED:
[1] Avsar, D. 1988; “Fisheries biology and
population dynamics.”, University of
Cukurova, Faculty of fisheries, Adana, Turkey,
p 303.
[2] Biswas, S. P. 1993; “Manual of method in fish
biology.” South Asian Publisher Pvt. Ltd. New
Delhi. Pp 145.
[3] Brewer, S. K. 2008; “Comparing histology and
Gonadosomatic Index for determining
spawning condition of small bodied riverine
fishes.” Ec. Fresh water fish. 17(i): 54-58.
[4] Hossain, M. Y. 2012; “Ovarian biology of
spotted snake head from natural Wetlands of
Sylhet, Bangladesh. 2(3): 64-76.
http://naturepub.org/archive/avas/v2/i3/AVAS.
2(3)-4.pdf
[5] James Milton. 2018; “Ovarian development and
histological observations of threatened dwarf
snakehead fish, C. gachua (Hamilton, 1822)”,
Saudi journal of Biological Sciences. 25 pp,
149-153.
[6] Kirti, T. 2014; “Study of gonadosomatic Index
of fresh water fish C. gachua”. Sci Res Pub
2014; 4(5): 1-2.
[7] Muchlisin, Z. A., M. Musman. 2010;
“Spawning seasons of Rasbora. towarensis.”
(Pices: Cyperinidae) in Lake Laut Tawar, Aceh
Province, Indonesia. Reproductive Biology and
Endocrinology, 8: 49-69.
[8] Nazir, B. M. 1978; “Annual cyclic changes in
testicular activity of a fresh water teleost,
Barbus Luteus (Hackel) from chatt-Al-Arab, I
IraqJ. Fish Biol. 13: 321-236
[9] Siddique, M. 2012. “Characterisation of C.
maurulius population in various water Bodies”,
Department of Environmental Sciences, Faculty
of Science and technology, GC University,
Faisalabad, Pakistan. pp 1-5.
[10] Sindhe, V. R. 2004. “Gonadosomatic
hepatosomatic indices of fresh water fish
Notopterus notopterus (pallas) in response to
some heavy metal exposure. J. Envison. Biol.,
25(3): 365-8.
[11] Quyam, A., Quasim, S. Z. 1966; “The growth
of the fresh water murrel, Ophiocephalus
punctatus Bloch. Hydrobiologia 27, 289-316.
[12] Vazzolar, A. E. A. de M. 1996; Biologia de
Reproducao de peixes Teleosteos: Teoria e
pratica. Eduem, Maringa p. 169.
[13] Winemiller, K. O. 1987; Feeding and
Reproductive Biology of the Currito,
Hoplosternum Littorale, Environmental
Biology of Fishes. 20: 219-227[pdf]

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Study on Sex Ratio and Gonadosomatic Index of Fresh Water Fish C. Gachua Ham.1822

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 6 Issue 3, March-April 2022 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 19 Study on Sex Ratio and Gonadosomatic Index of Fresh Water Fish C. Gachua (Ham.1822) Navjyoti Ranjan Verma Research Scholar, PG Department of Zoology, Tilka Manjhi Bhagalpur University, Bhagalpur, Bihar, India ABSTRACT Aspect of reproductive biology of fresh water murrel C. gachua, such as sex ratio and Gonadosomatic Index were investigated from the pools ,ditches and even from river Ganga in and around the area of Bhagalpur, Bihar for a complete year span. On the basis of the monthly variation, the overall sex ratio was recorded 1:1.22(M:F). The spawning season extends from June to August. Gonadosomatic Index in female fish reaches maximum in May with 44.50 %. The GSI recorded minimum in September with 5.71% followed by Oct with 7.21 %.GSI in male C. gachua was also studied and found the maximum in the month of June with 4.86%, closely followed by the month of July with 4.06%. The GSI was found the minimum in the month of January with 0.57% closely followed by the month of February with 0.84%. KEYWORDS: GSI, Spawning, Sex ratio How to cite this paper: Navjyoti Ranjan Verma "Study on Sex Ratio and Gonadosomatic Index of Fresh Water Fish C. Gachua (Ham.1822)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456- 6470, Volume-6 | Issue-3, April 2022, pp.19-22, URL: www.ijtsrd.com/papers/ijtsrd49449.pdf Copyright © 2022 by author(s) and International Journal of Trend in Scientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0) INTRODUCTION The reproductive biology of fish is greatly influenced by season. As fishes are seasonal breeder, the season affects its different reproductive aspects like sex ratio, GSI and even condition factor. With the approaching spawning all the reproductive aspects become maximum. The Gonadosomatic index of the fish increases with the maturation of fish, being maximum during the peak period of maturity and declining abruptly after spawning. The monthly studies were made to go through the GSI of C. gachua in detail. The spawning takes place between June to August every year. The sex ratio was also recorded for the complete year period. The findings clearly shows that the ratio of male and female fishes show an increment during the spawning season. Sex ratio also decreases after the spawning period ends, although it is very marginal. Nazir et. al. 1978 in Barbusleutus; Sindhe et. al. 2004 in Notopterus notopterusand many others have studied the same on various fishes. However no such studies were made on C. gachua, so this studiy is aimed on this dwarf snake headed murrel C. gachua. MATERIALS AND METHODS From the surrounding areas of Bhagalpur i.e. Bhairwa pond of T M Bhagalpur University campus, river Ganga, different pools and ditches, the dwarf snake headed C. gachua was collected monthly and brought to the laboratory. Studies were made on the fish to go through its GSI, sex ratio. Each of the fish was studied thoroughly before and after the dissection (removing its gonads) to go through its different reproductive aspects i.e. sex ratio and GSI. The present study is based on the sample brought to the laboratory. The sexes were counted and the ratio were calculated for all the seasons. Specimen were collected and measured for total length (cm/mm), total weight (gm), gonads wt. and length. Afterward the specimen were anesthetized, dissected and preserved in 10%formalin for further anatomical studies. Sex ratio: The sex and maturation stage of each specimen was determined nanoscopically considering coloration, transparency, superficial vascularization and for gonads the visualization and appearance of the ova and testis. IJTSRD49449
  • 2. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 20 The maturity stages of the male and female gonads were classified according to Biswas(1993) and computed monthly to ascertain the breeding season. The overall frequencies of the stages were also estimated. Spawning season was observed between June to August every year. GONADOSOMATIC INDEX (GSI) The GSI was calculated according to Vazzolar(1996): GSI= wt. of gonad/ total body weight ×100, was plotted monthly to identify the spawning. After calculating the GSI %, the period of maturity of fish was divided into four stages (Quyyam and Quasim, 1961) Ophiocephalus punctatus. 1. Pre spawning phase 2. Spawning phase 3. Post spawning phase 4. Preparatory phase It was observed that the Gonadosomatic index of fish increases during peak period of maturity and it declines abruptly post spawning. RESULT AND DISCUSSION SEX RATIO was studied in the laboratory. A total of 409 specimen of fishes were brought to laboratory for the study of gonads to find out the sex ratio (F: M) The superficial vascularization was made for the visualization and appearance of the gonads i.e. ovary and testis. The findings were collected in the form of Tab (A). Theaverage of the findings shows the ratio of 1. 22: 1(F: M) following chi-square method (X2 ). Tab (A) Sex ratio in C. gachua. Month Total no. of samples No. of Female % Female No. of Male % male Sex ratio (F: M) January 35 19 54. 29 16 45. 71 1. 18: 1 February 32 18 56. 25 14 43. 75 1. 28: 1 March 24 12 50. 50 12 50. 00 1. 00: 1 April 40 22 55. 00 18 45. 00 1. 22: 1 May 37 20 54. 06 17 45. 94 1. 17: 1 June 33 18 54. 55 15 45. 45 1. 20: 1 July 30 18 60. 00 12 40. 00 1. 50: 1 August 34 20 58. 83 14 41. 17 1. 42: 1 September 39 21 53. 85 18 46. 15 1. 16: 1 October 34 19 55. 89 15 44. 11 1. 26: 1 November 41 22 53. 66 19 46. 34 1. 15: 1 December 30 16 53. 34 14 46. 66 1. 14: 1 Total/Avg 409 225 55. 01 184 44. 99 1. 22: 1 GSI of C. gachua was estimated for females. Tab (B-1) shows the value of GSI (%) in females. GSI value rises from 13. 27 % in April to 20. 43% in June. It shows the pre spawning period. The GSI gradually decreases from 20. 43% in June to 15. 83 % in August. It means it is the spawning period. Furtheran abrupt decrease was observed from 12. 04% in September to 9. 55% in December. This phase can be said as post spawning phase. GSI in the month of January was calculated 5. 69% and is increased up to 11. 26 % in March indicating the preparatory period. GSI in male was observed the maximum in the month of maximum in the month of June with 4. 86%, closely followed by the month of July with 4. 06%. The GSI was found the minimum in the month of January with 0. 57% closely followed by the month of February with 0. 84%. From the above findings we observed that in C. gachua the peak value of the GSI is found only once in a year i.e. in the month of June, which clearly indicates only one spawning period in C. gachua i.e. from June to August. Similar observations were found by Nazir et al1978 in Barbus luetus; Brewer et al. 2008; Sindhe e. t al. 2004 in Notopterus notopterus; Brewer, 2008 in small riverine fishes, Mechalin Musri Musman, 2010 in Rasbora towarensis
  • 3. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 21 Tab. (B-1) GSI of female Channa gachua. Month Avg. Body wt. (gm) Avg Ovary wt. (gm) GSI % Sep 41. 5 5. 0 12. 04 Oct 38. 8 4. 1 10. 56 Nov 33. 0 3. 4 10. 30 Dec 31. 4 3. 0 9. 55 Jan 35. 1 2. 0 5. 69 Feb 35. 6 3. 1 8. 70 March 36. 4 4. 1 11. 26 April 36. 9 4. 9 13. 27 May 39. 0 7. 4 18. 97 June 46. 5 9. 5 20. 43 July 57. 4 11. 6 20. 20 August 44. 2 7. 0 15. 83 Chart (I) shows GSI % in Female C, gachua Table (B-2) GSI of male C. gachua Month Avg wt. of Fish(gm) Avg wt. of testis(gm) GSI % Jan 35. 0 0. 2 0. 57 Feb 35. 6 0. 3 0. 84 March 36. 2 0. 4 1. 10 April 37. 0 0. 7 1. 89 May 38. 0 1. 0 2. 63 June 43. 2 2. 1 4. 46 July 50. 6 2. 3 4. 06 August 42. 4 1. 0 2. 35 Sep 38. 5 0, 5 1. 29 Oct 35. 6 0. 7 1. 96 Nov 34. 2 0. 3 0. 87 Dec 32. 8 0. 2 0. 60
  • 4. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD49449 | Volume – 6 | Issue – 3 | Mar-Apr 2022 Page 22 Chart (II) showing GSI % in male C. gachua. LITERATURE CITED: [1] Avsar, D. 1988; “Fisheries biology and population dynamics.”, University of Cukurova, Faculty of fisheries, Adana, Turkey, p 303. [2] Biswas, S. P. 1993; “Manual of method in fish biology.” South Asian Publisher Pvt. Ltd. New Delhi. Pp 145. [3] Brewer, S. K. 2008; “Comparing histology and Gonadosomatic Index for determining spawning condition of small bodied riverine fishes.” Ec. Fresh water fish. 17(i): 54-58. [4] Hossain, M. Y. 2012; “Ovarian biology of spotted snake head from natural Wetlands of Sylhet, Bangladesh. 2(3): 64-76. http://naturepub.org/archive/avas/v2/i3/AVAS. 2(3)-4.pdf [5] James Milton. 2018; “Ovarian development and histological observations of threatened dwarf snakehead fish, C. gachua (Hamilton, 1822)”, Saudi journal of Biological Sciences. 25 pp, 149-153. [6] Kirti, T. 2014; “Study of gonadosomatic Index of fresh water fish C. gachua”. Sci Res Pub 2014; 4(5): 1-2. [7] Muchlisin, Z. A., M. Musman. 2010; “Spawning seasons of Rasbora. towarensis.” (Pices: Cyperinidae) in Lake Laut Tawar, Aceh Province, Indonesia. Reproductive Biology and Endocrinology, 8: 49-69. [8] Nazir, B. M. 1978; “Annual cyclic changes in testicular activity of a fresh water teleost, Barbus Luteus (Hackel) from chatt-Al-Arab, I IraqJ. Fish Biol. 13: 321-236 [9] Siddique, M. 2012. “Characterisation of C. maurulius population in various water Bodies”, Department of Environmental Sciences, Faculty of Science and technology, GC University, Faisalabad, Pakistan. pp 1-5. [10] Sindhe, V. R. 2004. “Gonadosomatic hepatosomatic indices of fresh water fish Notopterus notopterus (pallas) in response to some heavy metal exposure. J. Envison. Biol., 25(3): 365-8. [11] Quyam, A., Quasim, S. Z. 1966; “The growth of the fresh water murrel, Ophiocephalus punctatus Bloch. Hydrobiologia 27, 289-316. [12] Vazzolar, A. E. A. de M. 1996; Biologia de Reproducao de peixes Teleosteos: Teoria e pratica. Eduem, Maringa p. 169. [13] Winemiller, K. O. 1987; Feeding and Reproductive Biology of the Currito, Hoplosternum Littorale, Environmental Biology of Fishes. 20: 219-227[pdf]