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Article Citation:
Purbali Saha, Divya Singh, Bitopan Malakar, Santhosh Ram B., and Venu S.
Diversity and resource characteristics of Tetraodontidae fishes from Andaman with
special reference to Arothron immaculatus – a preliminary study
Journal of Research in Biology (2016) 6(2): 1984-1993
JournalofResearchinBiology
Diversity and resource characteristics of tetraodontidae fishes from
Andaman with special reference to Arothron immaculatus – a preliminary
study
Keywords:
Puffer fishes, Arothron, Canthigaster, Andaman, Reef fish
ABSTRACT:
Puffer fish belonging to the family tetraodontidae are usually distributed in
the shallow waters. During investigation in stations viz. Marina Park, Chidiyatapu and
Burmanullah, around Andaman, five species from genus Arothron and two from
Canthigaster have been recorded and were mostly found to prefer coral reefs and
rock crevices, with the exception of Arothron immaculatus, which was found to be
present in the open waters and it confined to sandy bottom substrate with patches of
sea grasses around them. These fishes were found to be most diverse and abundant in
Chidiyatapu with the Margelef’s Richness Index of 2.49, Shannon-Wiener index of 1.05
and Pielou’s evenness index of 0.96. Biometric analysis results demonstrate that they
have shown an isometric growth. The individuals collected were mostly lying in the
length group of 120-160 mm. Gut content analysis of A. Immaculatus reveals that the
fish feed mainly on molluscs and sea urchin and the other food items were shrimps,
crabs, sponges, micro algae, foraminiferans etc. gastro-somatic index, hepato-somatic
index and gonado-somatic indices were also calculated to throw light upon the feeding
behavior and reproductive maturity of the fishes. Most of the individuals were found
to be in the developing stage of maturity.
1984-1993| JRB | 2016 | Vol 6 | No 2
This article is governed by the Creative Commons Attribution License (http://creativecommons.org/
licenses/by/4.0), which gives permission for unrestricted use, non-commercial, distribution and
reproduction in all medium, provided the original work is properly cited.
www.jresearchbiology.com
Journal of Research in Biology
An International
Scientific Research Journal
Authors:
Purbali Saha,
Divya Singh,
Bitopan Malakar,
Santhosh Ram B and
Venu S
Institution:
Department of Ocean
Studies and Marine Biology
Pondicherry University, Port
Blair- 744112
Corresponding author:
Divya Singh
Email Id:
Web Address:
http://jresearchbiology.com/
documents/RA0570.pdf
Dates:
Received: 18 Dec 2015 Accepted: 25 Jan 2016 Published: 14 March 2016
Journal of Research in Biology
An International Scientific Research Journal
Original Research
ISSN No: Print: 2231 –6280; Online: 2231- 6299
INTRODUCTION
Puffer fish belong to the order Tetraodontiformes
under the family Tetraodontidae and are variously known
as the blowfish, toadfish, globefish, swellfish and
balloon fish (Halstead, 1967). They are found in the
tropical waters worldwide, but they rarely moves to the
cooler waters too. (Grant, 1987). Usually fish from the
order Tetradontiformes exhibit a typical swimming
behavior which is relatively slow, with their pectoral and
anal fins. They are morphologically well-defended from
predation by large dorsal-ventral spines (trigger fishes,
Balistidae), toxins, (puffers, Tetradontidae), and quill-
like scales (Porcupine fishes, Diodontidae), the latter two
families have fused dentition which is well adapted for
Saha et al., 2016
1985 Journal of Research in Biology (2016) 6(2):1984-1993
Figure 1. Location map showing all the study sites
Journal of Research in Biology (2016) 6(2):1984-1993 1986
Saha et al., 2016
consuming hard-shelled invertebrates. Puffer fish can
generally grow to upto 60 cm in length but the exact
length depends on the species, these fish can be found in
a diversity of colors but can occasionally be hard to
recognize when they are not inflated. It generally has the
appearance of a big tadpole, with protruding eyes and an
extended snout. They are omnivorous animals and eat an
assortment of plants and animals. Puffer fish mostly
forage on the algae that propagate on the rocks, corals
and also the invertebrates that inhabitats these parts.
Large species of puffer fish likewise feeds on shellfish
such as shrimp and crabs and molluscs and the
nutritional regime of milk spotted puffer Chelonodon
patoca (Beumer, 1978) and of the puffer S. spengleri and
S. testudineus (Targett, 1978) was largely dominated by
hard-shelled crustaceans and molluscs and numerous
examples of similar diet spectra have been observed for
the Tetraodontidae family (Krumme et al., 2007). Mostly
puffers possesses defense mechanisms to protect
themselves against predators: being poisonous, inflation
and aposematism (Krumme et al., 2007).
Immaculate puffer, Arothron immaculatus is a
comparatively friendly puffer and has the characteristic
form with a white greyish body without spots and has
been initially found in the Indo-Pacific Ocean but can as
well be found from the Red Sea and the East African
coast to Indonesia and Japan. They are found in the sea-
grass beds of shallow water or in mangrove forests and
are most common in estuaries and sea-grass beds. These
fishes are nocturnal in nature, carnivorous and feed on
Figure 2. (A) Arothron immaculatus (B) Arothron hispidus (C ) Canthigaster solandri
(D) Arothron nigropunctatus (E) Arothron reticularis (F) Canthigaster bennetti
shrimps, clams and mussels and benthic invertebrates
(Krumme et al., 2007). Sex differentiation of immaculate
puffer is hard but females are usually rounder than
males.
Tetradontids are the most common fish species
sampled from the tropical and sub-tropical mangroves
(Bell et al., 1984; Hindell and Jenkins, 2004). In the
Western Pacific, tetraodontids are commercially valuable
and highly regarded as fish food, even though the
presence of the family-specific tetradodoxin still causes
the death of gastronomers each year and later the puffer
fish were listed as ‘grey species’ in the reports by New
South Wales Fisheries (NSW DPI, 2006), which means
that this group requires further scientific or technical
consideration and risk assessment.
There are 29 genera of tetraodontidae that has
been documented by Froese and Pauly (2008) and
species of puffer fish detailed from tropical sea are about
120 (Sabrah et al., 2006), but only 20 puffer fish species
belonging to the family tetraodontidae has been
described from the Andaman and Nicobar Islands (Rajan
et al. 2013). The puffer fishes found in these islands are
not commercially important. They are generally
discarded by the fishermen since they are inedible
because of their toxicity. Even though there are many
works conducted on this group of fishes, but there is only
a single work so far been conducted from Andaman
water about the biology of puffer fishes (Kumar et al.,
2013), So the present study will give an idea about the
diversity and resource characters of these very important
fishes in the habitats around the island ecosystems.
MATERIALS AND METHODS
The present study was conducted between the
months of December 2013 to November 2014 in the
waters around Port Blair, South Andaman and the
stations investigated were Burmanallah, that mainly
comprised of rocky substratum; Chidiyatapu with well-
developed coral reef, mostly dominated by Porites spp.
and Marina Park that mainly comprises of sandy
substratum with patches of artificial reefs due to the
presence of the marina. All these three habitats provided
the fish with ample amount of food and shelter, thus a
large fish aggregation was observed in these areas. This
study investigated the diversity and abundance of the
species belonging to the genera Arothron and
Canthigaster along with the biology of Arothron
immaculatus.
The abundance of species were estimated by
using Fish belt transect method (Brock, 1954; English et
al., 1997). Shannon-Weiner index of diversity (Clarke
and Warwick, 2001) Margalef’s species richness index
(Clifford and Stephenson, 1975), Simpson Index
1987 Journal of Research in Biology (2016) 6(2):1984-1993
Saha et al., 2016
Figure 3. Fish composition during all the seasons at
Burmanallah
Figure 4. Fish composition during all the seasons at
Chidiyatapu
Figure 5. Fish composition during all the seasons at
Marina park
(Simpson, 1949) and Pielou’s species evenness index
(Hill, 1973) were used to estimate the evenness and
diversity of fishes.
A total of 20 specimens ranging from 115-190
mm TL and 45.2-100.6 g weight were collected at the
Marina Park and were analyzed for food and feeding
habits, sex ratio and stages of maturity, length-weight
relationships, hepatosomatic index, gastro-somatic index
and gonado-somatic index. Length weight relationship is
expressed by the formula W= aLb
(Le Cren 1951; Ricker
1973). Occurrence of each item was expressed as the
percentage of total number of stomach examined. In
order to determine the maturity stages, general
appearance of ovary like fullness in the ventral cavity,
size, shape and colour were considered. The
classification of maturity stages were made as per Qasim
(1972).
RESULTS AND DISCUSSION
A total of 105 individuals, that represents seven
species of puffer fishes (five from genus Arothron and
two from the genus Canthigaster) were observed, where
Journal of Research in Biology (2016) 6(2):1984-1993 1988
Saha et al., 2016
Figure 6. Various diversity indices for A. immaculatus in all the study sites
C1- Chidiyatapu (pre-monsoon); C2- Chidiyatapu (monsoon) ; C3- Chidiyatapu (post-monsoon) ; M1- Marina Park
(pre-monsoon); M2- Marina Park (monsoon) ; M3-Marina Park (post-monsoon) ; B1- Burmanullah (pre-monsoon);
B2- Burmanullah (monsoon); B3- Burmanullah (post-monsoon)
Figure. 7 Cluster analyses of all the three seasons at all the study sites
Species Group
average Transform: Square root
Resemblance: S17 Bray-Curtis similarity
Similarity
Stations
Arothron nigropunctatus was the most abundant species
and was observed at all the study sites and it accounts for
>25 % of the total number of total fish individuals
observed, while Arothron immaculatus, accounts for >
28%, but its existence was witnessed only at Marina
Park. The other species observed were Arothron hispidus
(8.57%), A. stellatus (14.29%), A. reticularis (5.71%),
Canthigaster bennetti (5.71%) and C. solandri (11.43%)
from all the study sites. Seasonal observations display
the higher abundance of all the puffer fishes during post-
monsoon (Fig. 3-5).
The values of Shannon-Wiener and Pielou’s
evenness Index showed high fish diversity at
Chidiyatapu along with a high abundance, these fishes
Saha et al., 2016
1989 Journal of Research in Biology (2016) 6(2):1984-1993
C1- Chidiyatapu (pre-monsoon); C2- Chidiyatapu (monsoon) ; C3- Chidiyatapu (post-monsoon) ; M1- Marina Park
(pre-monsoon); M2- Marina Park (monsoon) ; M3-Marina Park (post-monsoon) ; B1- Burmanullah (pre-monsoon); B2-
Burmanullah (monsoon); B3- Burmanullah (post-monsoon)
Figure 8. Numerical data of puffer fish abundance at all the study sites depicting changes in different seasons
Figure 9. Food and Feeding Habit of A. immaculatus Figure 10. Length-Weight Relationship
in A. immaculatus
were found to be evenly distributed and it could be due
to the vast area of bottom substratum covered with corals
and associated organisms which serve as feed for these
fishes.
While same values were found to be low in
Burmanullah and it showed very least diversity and the
number of individuals observed among different species
also varied to a wide margin indicating very low species
evenness. The reason could be the presence of rocky
shore that gets exposed to strong wave actions which
makes it less supportable for the fishes, particularly for
the slow moving puffer fishes. Although Marina Park
showed virtuous diversity and evenness of puffer fish
species its diverse substratum of rocks, reefs and sand
accommodating the puffer fish species was high .The
value for the Margalef species richness index was found
to be very high in Barmanullah indicating the presence of
a wide variety of reef fishes but in some or very few
numbers and Chidiyatapu showing a low richness but the
species present was more in numbers and evenly
distributed as well.
It can be clearly observed from Fig 7., that the
there were two revealing cluster formed when the
abundance data of all the three study sites clustered
Saha et al., 2016
Journal of Research in Biology (2016) 6(2):1984-1993 1990
Figure 11. Length frequency distribution of
A. immaculatus
Figure 12. Maturity stages of A. immaculatus
Figure 13. Sex wise Hepato-Somatic index, Gastro somatic Index and Gonado-Somatic Indices indicating the
reproductive maturity level of Arothron immaculatus.
#: Male; *: Female; GSI: Gonado-somatic Index; HSI : Hepato-somatic Index; GaSI: Gastro somatic Index
together and it revealed that Burmanullah site have
similar number of fish abundance at all the season while
the other stations showed proximity with each other in
the second cluster. In the Fig 8. Number wise data of
puffer fish has been displayed that is clearly indicating
the highest number of fishes in Marina Park during the
post-monsoon season.
The general feeding habit of puffers consists
mainly of hard-shelled crustaceans and molluscs and
small estuarine puffer fishes feed on resident benthic
fauna found often burrowed in the sediment. Very few
species have preference for algae and other invertebrates
as the teeth are modified into beak-like structures for
crushing the hard-shelled organisms. Present study has
also shown the same patterns in feeding habit, where the
fish mainly feeds on benthic organisms (Figure. 9),
where the maximum available content was found to be of
molluscan shells (32%) followed by sea urchin spines
(26%) and shrimp appendages (16%). In addition, crab
appendages (11%), foramaniferans (9%) and sponge
spicules (6%) were also in considerable proportions, and
it indicates the carnivorous nature of the fish. It has been
confirmed in other studies as well where the gut content
of the puffer fish mainly comprising of rock oysters
(71.66%), sea weed pieces (15.38%) and broken crab
shells (6.41%) (Kumar et al., 2013), while the puffer fish
Torquigener pleurogramma from Western Australia
feeds on polychaetes and amphipods for fish less that
130mm, and bivalve molluscs for larger fish (Potter et
al., 1988). Colomesus psittacus from North Brazilian
mangrove were specified predators of Cirripedia
(Balanus spp.) and crabs (Uca spp., Pachygrapsus
gracilis) (Krumme, et al., 2007). Tetractenos glaber in
Sydney estuaries feeds mainly on prawns, Semaphore
crabs Heloecius cordiformis, mussels and brown algae
(Alquezar et al., 2006), and the food of Lagocephalus
sceleratus from the Gulf of Suez, Egypt was composed
mainly of cephalopods (squids and cuttle fishes),
crustaceans (particularly crabs) and fishes (Sabrah et al.,
2006).
In the present study the analysis of length-weight
relationship of Arothron immaculatus was done to assess
its pattern of growth in pre-monsoon season. The b value
was found to be 2.9 which is a negative allometry (Fig.
10). Even though it shows almost an isometric growth
since it is very proximal to three. According to Bagenal
and Tesch (1978) b parameters generally do not vary
significantly throughout the year unlike parameter a that
may vary seasonally, daily and in different habitats (Can
et al., 2002). The length frequency observed in the
previous work done by Taskavak and Bilecenoglu, 2001
showed that the species of puffer fish (Lagocephalus
spadiceus) was found to be in the size range between 159
-199 mm. Similar works were done by Sabrah et al.
(2006), Michailidis (2010) and Aydin (2011) on
Lagocephalus scleratus which showed lengths within the
size ranges 185-785 mm, 60-770 mm and 125-630 mm
respectively. In this study the maximum numbers of
individuals were found to be in the size group between
150-160 mm (Fig. 11). The least number of individuals
were found among two size groups of 110-120 mm and
180-190 mm. The size range was between 115-190 mm
in the specimens analyzed and 50% of the individuals
were found to be male and another 50% as female (Fig.
12). Recent studies have revealed a proportional
relationship between toxicity and gonado-somatic index
suggesting that with the increase in GSI, the toxicity
increases (Ghosh et al., 2004). Tani, 1945, clearly
showed that the concentration of toxin per gram ovary
increased with the increase in the weight of the ovaries.
The maximum GSI was found to be 5.87 and the least
was 0.83 and it is shown in Figure 5. GSI values depicts
that most of the fishes have a more or less high GSI
indicating that they are approaching their spawning
season and hence the intensity of toxicity is also high.
GaSI (Gastro somatic Index) values for all the specimens
ranges in between 0.02 to 0.24 and HSI value was in
between 2.47 to 9.99 (Figure.13).
Saha et al., 2016
1991 Journal of Research in Biology (2016) 6(2):1984-1993
CONCLUSION
The biology study indicates that A. immaculatus
fish species are going to approach their spawning season
and length-weight relationship study specifies that the
maximum numbers of fishes are in150-160 mm length
group, which reveals that they are about to reach their
maturity stage and the same result was portrayed by GSI
values.
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Diversity and resource characteristics of tetraodontidae fishes from Andaman with special reference to Arothron immaculatus – a preliminary study

  • 1. Article Citation: Purbali Saha, Divya Singh, Bitopan Malakar, Santhosh Ram B., and Venu S. Diversity and resource characteristics of Tetraodontidae fishes from Andaman with special reference to Arothron immaculatus – a preliminary study Journal of Research in Biology (2016) 6(2): 1984-1993 JournalofResearchinBiology Diversity and resource characteristics of tetraodontidae fishes from Andaman with special reference to Arothron immaculatus – a preliminary study Keywords: Puffer fishes, Arothron, Canthigaster, Andaman, Reef fish ABSTRACT: Puffer fish belonging to the family tetraodontidae are usually distributed in the shallow waters. During investigation in stations viz. Marina Park, Chidiyatapu and Burmanullah, around Andaman, five species from genus Arothron and two from Canthigaster have been recorded and were mostly found to prefer coral reefs and rock crevices, with the exception of Arothron immaculatus, which was found to be present in the open waters and it confined to sandy bottom substrate with patches of sea grasses around them. These fishes were found to be most diverse and abundant in Chidiyatapu with the Margelef’s Richness Index of 2.49, Shannon-Wiener index of 1.05 and Pielou’s evenness index of 0.96. Biometric analysis results demonstrate that they have shown an isometric growth. The individuals collected were mostly lying in the length group of 120-160 mm. Gut content analysis of A. Immaculatus reveals that the fish feed mainly on molluscs and sea urchin and the other food items were shrimps, crabs, sponges, micro algae, foraminiferans etc. gastro-somatic index, hepato-somatic index and gonado-somatic indices were also calculated to throw light upon the feeding behavior and reproductive maturity of the fishes. Most of the individuals were found to be in the developing stage of maturity. 1984-1993| JRB | 2016 | Vol 6 | No 2 This article is governed by the Creative Commons Attribution License (http://creativecommons.org/ licenses/by/4.0), which gives permission for unrestricted use, non-commercial, distribution and reproduction in all medium, provided the original work is properly cited. www.jresearchbiology.com Journal of Research in Biology An International Scientific Research Journal Authors: Purbali Saha, Divya Singh, Bitopan Malakar, Santhosh Ram B and Venu S Institution: Department of Ocean Studies and Marine Biology Pondicherry University, Port Blair- 744112 Corresponding author: Divya Singh Email Id: Web Address: http://jresearchbiology.com/ documents/RA0570.pdf Dates: Received: 18 Dec 2015 Accepted: 25 Jan 2016 Published: 14 March 2016 Journal of Research in Biology An International Scientific Research Journal Original Research ISSN No: Print: 2231 –6280; Online: 2231- 6299
  • 2. INTRODUCTION Puffer fish belong to the order Tetraodontiformes under the family Tetraodontidae and are variously known as the blowfish, toadfish, globefish, swellfish and balloon fish (Halstead, 1967). They are found in the tropical waters worldwide, but they rarely moves to the cooler waters too. (Grant, 1987). Usually fish from the order Tetradontiformes exhibit a typical swimming behavior which is relatively slow, with their pectoral and anal fins. They are morphologically well-defended from predation by large dorsal-ventral spines (trigger fishes, Balistidae), toxins, (puffers, Tetradontidae), and quill- like scales (Porcupine fishes, Diodontidae), the latter two families have fused dentition which is well adapted for Saha et al., 2016 1985 Journal of Research in Biology (2016) 6(2):1984-1993 Figure 1. Location map showing all the study sites
  • 3. Journal of Research in Biology (2016) 6(2):1984-1993 1986 Saha et al., 2016 consuming hard-shelled invertebrates. Puffer fish can generally grow to upto 60 cm in length but the exact length depends on the species, these fish can be found in a diversity of colors but can occasionally be hard to recognize when they are not inflated. It generally has the appearance of a big tadpole, with protruding eyes and an extended snout. They are omnivorous animals and eat an assortment of plants and animals. Puffer fish mostly forage on the algae that propagate on the rocks, corals and also the invertebrates that inhabitats these parts. Large species of puffer fish likewise feeds on shellfish such as shrimp and crabs and molluscs and the nutritional regime of milk spotted puffer Chelonodon patoca (Beumer, 1978) and of the puffer S. spengleri and S. testudineus (Targett, 1978) was largely dominated by hard-shelled crustaceans and molluscs and numerous examples of similar diet spectra have been observed for the Tetraodontidae family (Krumme et al., 2007). Mostly puffers possesses defense mechanisms to protect themselves against predators: being poisonous, inflation and aposematism (Krumme et al., 2007). Immaculate puffer, Arothron immaculatus is a comparatively friendly puffer and has the characteristic form with a white greyish body without spots and has been initially found in the Indo-Pacific Ocean but can as well be found from the Red Sea and the East African coast to Indonesia and Japan. They are found in the sea- grass beds of shallow water or in mangrove forests and are most common in estuaries and sea-grass beds. These fishes are nocturnal in nature, carnivorous and feed on Figure 2. (A) Arothron immaculatus (B) Arothron hispidus (C ) Canthigaster solandri (D) Arothron nigropunctatus (E) Arothron reticularis (F) Canthigaster bennetti
  • 4. shrimps, clams and mussels and benthic invertebrates (Krumme et al., 2007). Sex differentiation of immaculate puffer is hard but females are usually rounder than males. Tetradontids are the most common fish species sampled from the tropical and sub-tropical mangroves (Bell et al., 1984; Hindell and Jenkins, 2004). In the Western Pacific, tetraodontids are commercially valuable and highly regarded as fish food, even though the presence of the family-specific tetradodoxin still causes the death of gastronomers each year and later the puffer fish were listed as ‘grey species’ in the reports by New South Wales Fisheries (NSW DPI, 2006), which means that this group requires further scientific or technical consideration and risk assessment. There are 29 genera of tetraodontidae that has been documented by Froese and Pauly (2008) and species of puffer fish detailed from tropical sea are about 120 (Sabrah et al., 2006), but only 20 puffer fish species belonging to the family tetraodontidae has been described from the Andaman and Nicobar Islands (Rajan et al. 2013). The puffer fishes found in these islands are not commercially important. They are generally discarded by the fishermen since they are inedible because of their toxicity. Even though there are many works conducted on this group of fishes, but there is only a single work so far been conducted from Andaman water about the biology of puffer fishes (Kumar et al., 2013), So the present study will give an idea about the diversity and resource characters of these very important fishes in the habitats around the island ecosystems. MATERIALS AND METHODS The present study was conducted between the months of December 2013 to November 2014 in the waters around Port Blair, South Andaman and the stations investigated were Burmanallah, that mainly comprised of rocky substratum; Chidiyatapu with well- developed coral reef, mostly dominated by Porites spp. and Marina Park that mainly comprises of sandy substratum with patches of artificial reefs due to the presence of the marina. All these three habitats provided the fish with ample amount of food and shelter, thus a large fish aggregation was observed in these areas. This study investigated the diversity and abundance of the species belonging to the genera Arothron and Canthigaster along with the biology of Arothron immaculatus. The abundance of species were estimated by using Fish belt transect method (Brock, 1954; English et al., 1997). Shannon-Weiner index of diversity (Clarke and Warwick, 2001) Margalef’s species richness index (Clifford and Stephenson, 1975), Simpson Index 1987 Journal of Research in Biology (2016) 6(2):1984-1993 Saha et al., 2016 Figure 3. Fish composition during all the seasons at Burmanallah Figure 4. Fish composition during all the seasons at Chidiyatapu Figure 5. Fish composition during all the seasons at Marina park
  • 5. (Simpson, 1949) and Pielou’s species evenness index (Hill, 1973) were used to estimate the evenness and diversity of fishes. A total of 20 specimens ranging from 115-190 mm TL and 45.2-100.6 g weight were collected at the Marina Park and were analyzed for food and feeding habits, sex ratio and stages of maturity, length-weight relationships, hepatosomatic index, gastro-somatic index and gonado-somatic index. Length weight relationship is expressed by the formula W= aLb (Le Cren 1951; Ricker 1973). Occurrence of each item was expressed as the percentage of total number of stomach examined. In order to determine the maturity stages, general appearance of ovary like fullness in the ventral cavity, size, shape and colour were considered. The classification of maturity stages were made as per Qasim (1972). RESULTS AND DISCUSSION A total of 105 individuals, that represents seven species of puffer fishes (five from genus Arothron and two from the genus Canthigaster) were observed, where Journal of Research in Biology (2016) 6(2):1984-1993 1988 Saha et al., 2016 Figure 6. Various diversity indices for A. immaculatus in all the study sites C1- Chidiyatapu (pre-monsoon); C2- Chidiyatapu (monsoon) ; C3- Chidiyatapu (post-monsoon) ; M1- Marina Park (pre-monsoon); M2- Marina Park (monsoon) ; M3-Marina Park (post-monsoon) ; B1- Burmanullah (pre-monsoon); B2- Burmanullah (monsoon); B3- Burmanullah (post-monsoon) Figure. 7 Cluster analyses of all the three seasons at all the study sites Species Group average Transform: Square root Resemblance: S17 Bray-Curtis similarity Similarity Stations
  • 6. Arothron nigropunctatus was the most abundant species and was observed at all the study sites and it accounts for >25 % of the total number of total fish individuals observed, while Arothron immaculatus, accounts for > 28%, but its existence was witnessed only at Marina Park. The other species observed were Arothron hispidus (8.57%), A. stellatus (14.29%), A. reticularis (5.71%), Canthigaster bennetti (5.71%) and C. solandri (11.43%) from all the study sites. Seasonal observations display the higher abundance of all the puffer fishes during post- monsoon (Fig. 3-5). The values of Shannon-Wiener and Pielou’s evenness Index showed high fish diversity at Chidiyatapu along with a high abundance, these fishes Saha et al., 2016 1989 Journal of Research in Biology (2016) 6(2):1984-1993 C1- Chidiyatapu (pre-monsoon); C2- Chidiyatapu (monsoon) ; C3- Chidiyatapu (post-monsoon) ; M1- Marina Park (pre-monsoon); M2- Marina Park (monsoon) ; M3-Marina Park (post-monsoon) ; B1- Burmanullah (pre-monsoon); B2- Burmanullah (monsoon); B3- Burmanullah (post-monsoon) Figure 8. Numerical data of puffer fish abundance at all the study sites depicting changes in different seasons Figure 9. Food and Feeding Habit of A. immaculatus Figure 10. Length-Weight Relationship in A. immaculatus
  • 7. were found to be evenly distributed and it could be due to the vast area of bottom substratum covered with corals and associated organisms which serve as feed for these fishes. While same values were found to be low in Burmanullah and it showed very least diversity and the number of individuals observed among different species also varied to a wide margin indicating very low species evenness. The reason could be the presence of rocky shore that gets exposed to strong wave actions which makes it less supportable for the fishes, particularly for the slow moving puffer fishes. Although Marina Park showed virtuous diversity and evenness of puffer fish species its diverse substratum of rocks, reefs and sand accommodating the puffer fish species was high .The value for the Margalef species richness index was found to be very high in Barmanullah indicating the presence of a wide variety of reef fishes but in some or very few numbers and Chidiyatapu showing a low richness but the species present was more in numbers and evenly distributed as well. It can be clearly observed from Fig 7., that the there were two revealing cluster formed when the abundance data of all the three study sites clustered Saha et al., 2016 Journal of Research in Biology (2016) 6(2):1984-1993 1990 Figure 11. Length frequency distribution of A. immaculatus Figure 12. Maturity stages of A. immaculatus Figure 13. Sex wise Hepato-Somatic index, Gastro somatic Index and Gonado-Somatic Indices indicating the reproductive maturity level of Arothron immaculatus. #: Male; *: Female; GSI: Gonado-somatic Index; HSI : Hepato-somatic Index; GaSI: Gastro somatic Index
  • 8. together and it revealed that Burmanullah site have similar number of fish abundance at all the season while the other stations showed proximity with each other in the second cluster. In the Fig 8. Number wise data of puffer fish has been displayed that is clearly indicating the highest number of fishes in Marina Park during the post-monsoon season. The general feeding habit of puffers consists mainly of hard-shelled crustaceans and molluscs and small estuarine puffer fishes feed on resident benthic fauna found often burrowed in the sediment. Very few species have preference for algae and other invertebrates as the teeth are modified into beak-like structures for crushing the hard-shelled organisms. Present study has also shown the same patterns in feeding habit, where the fish mainly feeds on benthic organisms (Figure. 9), where the maximum available content was found to be of molluscan shells (32%) followed by sea urchin spines (26%) and shrimp appendages (16%). In addition, crab appendages (11%), foramaniferans (9%) and sponge spicules (6%) were also in considerable proportions, and it indicates the carnivorous nature of the fish. It has been confirmed in other studies as well where the gut content of the puffer fish mainly comprising of rock oysters (71.66%), sea weed pieces (15.38%) and broken crab shells (6.41%) (Kumar et al., 2013), while the puffer fish Torquigener pleurogramma from Western Australia feeds on polychaetes and amphipods for fish less that 130mm, and bivalve molluscs for larger fish (Potter et al., 1988). Colomesus psittacus from North Brazilian mangrove were specified predators of Cirripedia (Balanus spp.) and crabs (Uca spp., Pachygrapsus gracilis) (Krumme, et al., 2007). Tetractenos glaber in Sydney estuaries feeds mainly on prawns, Semaphore crabs Heloecius cordiformis, mussels and brown algae (Alquezar et al., 2006), and the food of Lagocephalus sceleratus from the Gulf of Suez, Egypt was composed mainly of cephalopods (squids and cuttle fishes), crustaceans (particularly crabs) and fishes (Sabrah et al., 2006). In the present study the analysis of length-weight relationship of Arothron immaculatus was done to assess its pattern of growth in pre-monsoon season. The b value was found to be 2.9 which is a negative allometry (Fig. 10). Even though it shows almost an isometric growth since it is very proximal to three. According to Bagenal and Tesch (1978) b parameters generally do not vary significantly throughout the year unlike parameter a that may vary seasonally, daily and in different habitats (Can et al., 2002). The length frequency observed in the previous work done by Taskavak and Bilecenoglu, 2001 showed that the species of puffer fish (Lagocephalus spadiceus) was found to be in the size range between 159 -199 mm. Similar works were done by Sabrah et al. (2006), Michailidis (2010) and Aydin (2011) on Lagocephalus scleratus which showed lengths within the size ranges 185-785 mm, 60-770 mm and 125-630 mm respectively. In this study the maximum numbers of individuals were found to be in the size group between 150-160 mm (Fig. 11). The least number of individuals were found among two size groups of 110-120 mm and 180-190 mm. The size range was between 115-190 mm in the specimens analyzed and 50% of the individuals were found to be male and another 50% as female (Fig. 12). Recent studies have revealed a proportional relationship between toxicity and gonado-somatic index suggesting that with the increase in GSI, the toxicity increases (Ghosh et al., 2004). Tani, 1945, clearly showed that the concentration of toxin per gram ovary increased with the increase in the weight of the ovaries. The maximum GSI was found to be 5.87 and the least was 0.83 and it is shown in Figure 5. GSI values depicts that most of the fishes have a more or less high GSI indicating that they are approaching their spawning season and hence the intensity of toxicity is also high. GaSI (Gastro somatic Index) values for all the specimens ranges in between 0.02 to 0.24 and HSI value was in between 2.47 to 9.99 (Figure.13). Saha et al., 2016 1991 Journal of Research in Biology (2016) 6(2):1984-1993
  • 9. CONCLUSION The biology study indicates that A. immaculatus fish species are going to approach their spawning season and length-weight relationship study specifies that the maximum numbers of fishes are in150-160 mm length group, which reveals that they are about to reach their maturity stage and the same result was portrayed by GSI values. REFERENCES Alquezar R, Markich SJ and Booth DJ. (2006). Metal accumulation in the smooth toadfish, Tetractenos glaber, in estuaries around Sydney, Australia. Environmental Pollution, 142(1): 116-122. Aydin M. (2011). Growth, reproduction and diet of pufferfish (Lagocephalus sceleratus Gmelin, 1789) from Turkey’s Mediterranean Sea Coast. Turkish Journal of Fisheries and Aquatic Sciences, 11(4): 589-596. Bagenal TB and Tesch FW. (1978). Age and growth. In: Methods for assessment of fish production in fresh waters, 3rd edn. T. Bagenal (Ed.). IBP Handbook. Blackwell Science Publications, Oxford, (3): 101–136. Bell JD, Pollard DA, Burchmore JJ, Pease BC and Middleton MJ. (1984). Structure of a fish community in a temperate tidal mangrove creek in Botany Bay, New South Wales. Australian Journal of Marine and Freshwater Research, 35(1): 33-46. Beumer JP. (1978). Feeding ecology of four fishes from a mangrove creek in north Queensland, Australia. Journal of Fish Biology, 12(5): 475-490. Brock VE. (1954). A preliminary report on a method of estimating reef fish populations. Journal of Wildlife Management, 18(3): 297-308. Can MF, Basuta N and Cekic M. (2002). Weight length relationships for selected fish species of the small- scale fisheries off the south coast of Iskenderun Bay. Turkish Journal of Veterinary and Animal Sciences, 26(5): 1181-1183. Clarke KR and Warwick RM. (2001). Changes in marine communities: an approach to statistical analysis and interpretation, 2nd edition, PRIMERE: Plymouth. 172. Clifford HT and Stephenson W. (1975). An introduction to numerical classification. Academic Press, London. English S, Wilkinson C and V Baker. (1997). Survey Manual for Tropical Marine Resources. Townsville, Australia, Australian Institute of Marine Science, Townsville Australia. 378. Froese R and Pauly. (2008). Family Tetraodontidae- Puffers [Electronic Version]. Retrieved 29 December 2009. Ghosh S, Hazra AK, Banerjee S and Biswapati Mukherjee (2004). The seasonal toxicological profile of four puffer fish species collected along Bengal coast, India. Indian Journal of Marine Sciences, 33(3): 276- 280. Grant E. (1987). Fishes of Australia. E.M. Grant PTY Limited. Redcliffe, Australia. Hindell JS and Jenkins GP. (2004). Spatial and temporal variability in the assemblage structure of fishes associated with mangroves (Avicennia marina) and intertidal mudflats in temperate Australian embayments. Marine Biology, 144(2): 385-395. Hill MO (1973). Diversity and evenness: a unifying notation and its consequences. Ecology, 54(2)427-473. Halstead B (1967). Poisonous and venomous marine animals of the world, US Government Printing Office, Washington DC. Krumme U, Keuthen H, Saint-Paul U and Villwock Saha et al., 2016 Journal of Research in Biology (2016) 6(2):1984-1993 1992
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