reproductive biology of blue tang fish ( paracanthurus...
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Indian Journal of Geo Marine Sciences
Vol. 47 (04), April 2018, pp. 839-845
Reproductive biology of blue tang fish (Paracanthurus hepatus Linnaeus, 1776) in
Khanh Hoa seawater, Viet Nam
Huynh Minh Sang* & Ho Son Lam
Aquaculture Department - Institute of Oceanography, Vietnam Academy of Science and Technology,
01 Cau Da, Nha Trang, Viet Nam *[Email: [email protected]]
Received 23 August 2016 ; revised 28 November 2016
Blue tang fish (Paracanthurus hepatus Linnaeus, 1776) is one of the most popular fish caught in Khanh Hoa seawaters
for aquarium. A study on reproductive biology was conducted to evaluated the reproductive parameters including gonadal
development stages, sex ratio, spawning season, fecundity and size at first sexual maturity. Results showed that, number of
male and female in the nature was not significantly different. Gonadal of the fish passed through five stages of maturation.
The histological screening of gonad, percentage of maturation stage and gonadal somatic index value of the fish showed all
year round spawning with a peak of spawning female from April to September. Length at first sexual maturity of the fish
was 149.2 mm. Fecundity ranged from 1.527 – to 20.618 ovaries/ and strongly related to weight and length.
[Key word: blue tang, Paracanthurus hepatus, reproductive biology, Khanh Hoa]
Introduction The reproductive cycles of fishes are closely tied to
the environmental changes particularly temperature,
photoperiod and food supply1. Reproductive
parameters, such as gonadal development stages, sex
ratio, sex at first maturity, spawning season,
fecundity, are of great value in fishery resource
management and also essential and important in
aquaculture practices. The availability of quality seeds
and the ability to control fish reproduction are widely
recognized as limiting factors in the farming of any
commercial species2.
Blue tang fish (Paracanthurus hepatus Linnaeus,
1776) is a species of Indo-Pacific surgeonfish. This
fish is found from East Africa to Micronesia, Line
Islands and Samoa Islands, northwards to Kochi
Prefecture, southwards to New South Wales,
Australia. As a popular fish in marine aquarium, and
it is the only member of the genus Paracanthurus. The
species' range is broad, but it is common nowhere.
The fish can be found throughout the Indo-Pacific. It
is seen in the reefs of the Philippines, Indonesia,
Japan, the Great Barrier Reef of Australia, New
Caledonia, Samoa, Florida, East Africa, and Sri
Lanka, Vietnam. The blue tang is one of the most
common and most popular marine aquarium fish all
over the world. They live in pairs, or in small groups
of 8 to 14 individuals. These fish reach sexual
maturity at 9–12 months of age3.
Increasing demand for ornamental purposes of the
blue tang fish have been affecting in the natural
resource of this fish in Khanh Hoa seawater. A survey
data conducted to evaluation the natural caught of this
fish in Khanh Hoa has shown that total number caught
per year did not exceed 1000 individual4. Thus, there
is a great need for a suitable management strategy of
the natural resource of the fish as well as the strategy
for also breeding of this fish supporting for
ornamental aquarium, reducing the impact on natural
resource. However, information available on the
reproductive biology of this fish in Khanh Hoa
seawaters is still unknown. Hence, a detail
investigation on reproductive biology including
gonadal development stages, sex ratio, spawning
season, fecundity and size at first sexual maturity was
conducted and the results are presented and discussed
in this paper.
Material and Methods
Blue tang fish was collected from the fishing boat
fishing in Nha Trang bay and Spattly Island, Khanh
Hoa seawater from January 2015 to December, 2015.
The fish boat used trammel net, diving catch to collect
the fish. The size of fishes ranged from 30 to 180 mm
INDIAN J. MAR. SCI., VOL. 47, NO. 04, APRIL 2018
840
in total length. Around 30 fishes was collected each
month. The number of fish collect each month is
presented at Table 1.
The fishes was transported to laboratory at the
Institute of Oceanography, Vietnam for analysis. At the
laboratory the fishes were killed using ice-slurry
immersion method then weighed and measure the
length. Reproductive gonad of the fish (testes or ovaries)
were then dissected and weighed for further analysis.
While the maturity stages of females were
recognized based on the macroscopic appearance of
the ovary in the body cavity and microscopic structure
of ova, in males only the macroscopic appearance of
testes was considered. Gonadal development stages of
fishes were determined by methods of Nikolsky5 and
Xakun & Buskaia6 using Olympus BX50 microscope
at 10 X and 40 X magnification.
Histological analysis of testes and ovary was
performed following the method described by Gen
et al. (2007). Ovary or testes of each gonadal
development stage of fish were dissected and fixed in
4% buffer formalin for 24 h. After dehydrating by
passing the tissue through a series of alcohol solutions
of 70, 85 and 98%, the samples were vacuum
embedded in paraffin. The histological sections
(4 -5µm) were stained for general morphological
purposes with hematoxylin and eosin (H&E). The
samples were photographically analyzed and
documented using the Olympus BX 50 microscope at
40 X magnification.
Spawning season of the species was determined
based on the availability of mature and spent
individuals in the commercial landings during different
months and the monthly gonado-somatic indices (GSI).
The GSI was calculated7&8
using the formula:
GSI = 100 * (GW/BW) where GW is weight of gonad
and BW is weight of fish.
To estimate the length at first maturity (Lm), females,
were grouped separately into 6 mm class intervals and
fish in stage III and above were considered mature.
Length at first sexual maturity (Lm) were defined as the
length at which 50 per cent of all female fish having
ovaries at advanced stage of development according to
King9. The proportion of the female fish have ovaries at
advanced stage of development (P) of each size group
was adjusted by correction factor as the the biggest size
group was 100%. The linear relationship between size
group and Ln(1-P/P) was determined and the Lm was
calculated at P = 0.5.
Sex ratio was determined by the ratio of number of
male and female. Chi-square test was used to test the
different between the number of male and females in
the natural population of the fish.
To estimate fecundity, 30 ovaries in stage – IV
were utilised. From formalin preserved ovary of
known weight, a small portion was removed and
weighed to the nearest 0.001 g in an electronic
balance and then kept in modified Gilson’s fluid10
for
two days. All the oocytes in the sample ovary were
counted under binocular microscope using a counting
chamber. The absolute fecundity was estimated using
the formula: Absolute Fecundity (F) = (weight of
ovary/weight of sample) x number of oocytes in the
sample. The relationship between fecundity and total
length and weight statically determined using the
following formula: LogF = aLogX + b where F is
demoted fecundity, X is total length or weight, a and
b are constant. Relative fecundity was calculated
using the following formula: S=F/W where S is
relative fecundity W is fish weight (g).
Results The maturity stages of ovary and testes of blue tang
fish in Khanh Hoa was represented as in Tables 2 and 3.
Table 1 — Number of fish collected each month during 2015
Month No Month No
Jan 30 Jul 31
Feb 30 Aug 30
Mar 30 Sep 37
Apr 31 Oct 30
May 32 Nov 30
Ju 32 Dec 30
Table 2 — Maturity stages of female blue tang fish in Khanh Hoa
Maturity stages Particular of the gonads
Stage I, Immature Ovary was thin, short and glassy in appearance. It could not be distinguished ovary and testes by snake-eyes.
The stages was observed in the fish size under the first maturation size.
Stage II, Maturing Ovary developing, ovary and testes can be distinguished by snake-eyes. Ovaries are opaque and creamy
yellow.
Stage III, Mature Ovaries increase the size comparing to stage II. Ovaries are reddish yellow, extending about 2/3 body cavity
length.
Stage IV, Ripe/Oozing Ovaries are yellow to amber colored filling the entire body cavity, extending in the entire body cavity length
Stage V, Spent Ovaries are rather flaccid, reddish yellow.
SANG & LAM et al.: BIOLOGY OF BLUE TANG FISH (PARACANTHURUS HEPATUS LINNAEUS, 1776)
841
The histology of ovaries and testes of the blue tang
fish in Khanh Hoa are presented as Figs. 1 and 2.
Ratio of male and female of blue tang fish in
Khanh Hoa seawaters was 1:1,07. Number of male
and female was not significantly different (χ2 = 0,
45 < 3, 845 (df = 1, P < 0,05)).
The fishes at mature (III) and ripe stages (IV) of
ovaries presented all year round. However,
percentages of fish at maturation stages of III, IV and
V was higher during the priod from March to August
than that during the period from September to
February (Fig. 3). Percentages of advance stage of
ovaries (IV and V) in July was the highest (81 %) and
the lowest was in January 47 (%).
GSI of the female blue tang fish in Khanh Hoa
seawater was highest in March (0,65 ± 0,24), and
lowest was in October (0,22 ± 0,08). For the male
blue tang fish, the highest GSI was in February
Fig. 1 — Histological sections of ovaries of the blue tang fish in Khanh Hoa
Note: A, B, C & D is the histological section of the ovaries at II, III, IV & V maturity stage, respectively; Evtg: early vitellogenic oocyte;
AVtg: advanced vitellogenic oocyte; PG: primary growth oocyte; y: yolk vesicles; n: nucleus.
INDIAN J. MAR. SCI., VOL. 47, NO. 04, APRIL 2018
842
(0,22 ± 0,13) to April (0,22 ± 0,1), and the lowest GSI
was observed in October (0,14 ± 0.04) (Fig. 4).
The length of the first sexually maturity of the blue tang fish in
Khanh Khoa seawater was counted at 149.2 mm (Fig. 5).
Fig. 2 — Histological images of the testes of of the blue tang fish in Khanh Hoa
Spc: spermatocytes; Spm: spermatids; Spz: spermatozoa; Sc: Sertoli cells; L: seminiferous lobule; It: interstitialtissue.
Table 3 — Maturity stages of male blue tang fish in Khanh Hoa
Maturity stages Particular of the gonads
Stage I, Immature Testes was thin, short and glassy in appearance. It could not be distinguished ovary and testes by snake-eyes. The
stages was observed in the fish size under the first maturation size.
Stage II, Maturing Testes start developing, ovary and testes can be distinguished by snake-eyes. Testes are moderately thick,
flattened and white.
Stage III, Mature Testes increase the size comparing to stage II. Testes are flat, well-developed and creamy white, extending about
2/3 body cavity length
Stage IV,
Ripe/Oozing
Testes are very thick, flat, turgid and creamy, extending in the entire body cavity length
Stage V, Spent Testes are sunken
SANG & LAM et al.: BIOLOGY OF BLUE TANG FISH (PARACANTHURUS HEPATUS LINNAEUS, 1776)
843
The absolute fecundity of the blue tang tang fish in
Khanh Hoa varied from 1.527 – to 20.618
ovaries/individual with an average of 9.983 ± 6.026
ovaries/individual. Relative fecundity of the fish
varied from 28 to 92 with an average of
67 ± 19 ova/gram of females fish. The relationship
between fecundity and the length and weight of fish
was presented as in Fig. 6 and 7.
Discussion
Understanding of the reproductive biology of fish
is necessary for fishery resource management and
aquaculture practices. This is the first attempt to
Fig. 6 — Fecundity - total length relationship of the blue tang fish
in Khanh Hoa
Fig. 7 — Fecundity - total weight relationship of the blue tang fish
in Khanh Hoa
Fig. 3 — Monthly percentages of maturation stages of blue tang fish
Fig. 4 — Monthly change of the GSI of blue tang fish in Khanh Hoa
Fig. 5 — Groups of size relationship and Ln ((1-P) / P) of the blue
tang fish in Khanh Hoa
y = 4.581x - 6.581
R² = 0.935
2.5
3
3.5
4
4.5
5
2.1 2.2 2.3 2.4 2.5
Lo
g F
Log (TL)
y = 1.535x + 0.683
R² = 0.913
2.5
2.7
2.9
3.1
3.3
3.5
3.7
3.9
4.1
4.3
4.5
1.5 2 2.5
Lo
g F
Log BW
0
10
20
30
40
50
60
70
80
90
100Ja
nu
ary
Feb
ruar
y
Mar
ch
Ap
ril
May
Jun
e
July
Au
gu
st
Sep
tem
…
Oct
ob
er
No
vem
ber
Dec
emb
er
Per
cen
tage
(%
)
Month
Stage VStage IVStage IIIStage IIStage I
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
Jan
uar
y
Feb
ruar
y
Mar
ch
Ap
ril
May
Jun
e
July
Au
gu
st
Sep
te…
Oct
ob
er
No
ve…
Dec
e…
GS
I %
Month
Male
y = -0.053x + 7.908
R² = 0.922
-2
-1.5
-1
-0.5
0
0.5
1
1.5
2
110 130 150 170 190Ln
(1-P
)/P
Length (mm)
INDIAN J. MAR. SCI., VOL. 47, NO. 04, APRIL 2018
844
investigate some reproductive parameters of the blue
tang fish. In this study, the gonad of the blue tang fish
was divided into 5 stages of maturity. This is
normally observed in the tropical fish having the year
round reproduction cycles. At mature or ripe stages,
beside the main component oocytes (oocyte at early
vitellogenic and advanced vitellogenic stage), the
primary growth oocytes also exist at the considerate
number. This is the evidence that blue tang fish
spawn continuously during the spawning season. In
addition, the data on the changes in percentage of
maturity stages and GSI in the current study suggests
that, blue tang fish in Khanh Hoa spawn all year
round with a peak season from April to September.
This results is consistent with others studies on
tropical marine fishes. Fishes in estuary and coastal
seawater all most spawning year round and have one
peak spawning season11&12
. The peak spawning
season of the blue tang fish in Khanh Hoa is similar
to the anemone fish (Amphiprion sp)13
and in
contrast with sliver sillago (Sillaga sihama) (from
December to April)14
. According to Vijay Anand and
Pillai15
the peak spawning season of some species
belonging to family Acanthuridae is different with
the blue tang fish in the current study. Acanthlinis
leucosternon, A. triostegus, Chaetodon collare,
Plectorhinchus orientalis, Parupeneus bifasciatus
have peak spawning season from September to
April, November to May, February to April,
December to May and September to April,
respectively. The different in peak spawning season
and of the different fish species may due to the
species biology and environmental condition.
Fecundity of fishes is usually determined from the
number of ova of the mature group in the ovary. In
the present study, fecundity of Paracanthurus
hepatus, was determined from the examination of
30 specimens. In the present study, fecundity showed
high correlation coefficient with the total length of the
fish. The regression of fecundity and total length can
be expressed as Log F = 4.581*Log (TL) – 6.581 with
R2 value was 0.935. The regression of fecundity and
body weight can be expressed as Log F = 1.535*Log
(BW) + 0.683 with R2 value was 0.913. The absolute
fecundity of blue tang fish in Khanh Hoa seawater is
equivalent to the fecundity of other aquarium fish
such as Chaetodon trifasciatus (1.984-21.975) and
C. melannotris (1.492-24.532)15
. By contrast, this
value is higher than other fish such as Thalassoma
lunare (3.342-10.360); Parupeneus barberinus
(9.234-10.988) Thalassoma hardwicki (4.600-8.743)
và Chaetodon octofasciatus (1.060-2.879)15
; and
lowest than Chaetodon collare (2.763-31.065) and
Parupeneus bifasciatus (2.968-146.373)15
. Similar to
other fish, fecundity of the blue tang fish in the
current study is positive correlated to total length.
This finding suggests that total ovaries in a spawning
season depend on the fish size16
.
Sex ratio of the blue tang fish in the current study was
approximate 1:1. The result is in consistent with other
fish such as Acanthlinis leucosternon15
. However, the
ratio is diffent to others species such as A. triostegus
Chaetodon collare; Plectorhinchus orientalis;
Thalassoma hardwicki15
.
The length at sexual maturity of the blue tang fish
in Khanh Hoa seawater in the current study is larger
than that of two other fish belonging to family
Acanthuridae: Acanthlinis leucosternon (101 -120 cm)
and A. triostegus (71-100 cm)15
. This may due to the
species characteristics and the maximum size as well
as the life cycle of the fishes.
Conclusion The present study reveals that blue tang fish in
Khanh Hoa seawater spawns year round which peak
season from April to September, length at first sexual
maturity of the fish is 149.2 mm. Fecundity ranged
from 1.527 – to 20.618 ovaries/ and strongly related
to weight and length. The currently findings provide
the scientific foundation for the purpose of fishery
resource management and artificial breeding of the
blue tang fish.
Acknowledgments The authors are grateful to Ms. Nguyen Tuong Vy,
Ms. Phan Thi Ngoc for contributing to sample collection
and analysis. This work is finacially supported by
Vietnam Academy of Science and Technology (VAST)
under the project number VAST06.04/15-16.
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