Based on morphological characteristic,
the research detected 8 digeneans species
of 8 genera, of which 6 are unidentified at the
species level. Prevalence and intensity ranged
from 4–63.63% and 1–22, respectively. The
highest (63.63%) and lowest (4%) prevalence
is for Tubulovesicula sp. and Cholepotes sp.
and Carneohallus sp., respectively. The
highest (22) and lowest (1) intensity is for
Cholepotes sp., Bivesicula claviformis,
Carneohallus sp., Allobacciger diplorchis and
Tubulovesicula sp., respectively.
6 trang |
Chia sẻ: huongthu9 | Lượt xem: 459 | Lượt tải: 0
Bạn đang xem nội dung tài liệu Digenean diversity of reef fishes in Khanh Hoa province, Viet nam, để tải tài liệu về máy bạn click vào nút DOWNLOAD ở trên
Journal of Fisheries science and Technology Special issue - 2015
NHA TRANG UNIVERSITY • 23
DIGENEAN DIVERSITY OF REEF FISHES
IN KHANH HOA PROVINCE, VIET NAM
Dang Thuy Binh1, Tran Quang Sang2, Dang Nguyen Anh Tuan2
ABSTRACT
Coral reefs are massive areas of calcium carbonate in the oceans and are among the ecosystems having
high biodiversity, including 700 coral species, 600 mollusks, and nearly 4,000 fishes. Research on the parasites
that infect Vietnamese coral reef fish are limited. Examinations of 116 individuals of 9 reef fishes have been
conducted to date. We have detected 8 digeneans (Bivesicula claviformis, Lecithochirium sp., Allobacciger
diplorchis, Cainocreadium labracis, Cholepotes sp., Carneophallus sp., Tubulovesicula sp. and Tetrochetus
sp.). Two clownfishes and a goatfish were infected by two species, while only 1 digenean infected all remaining
fishes. The highest (63.63%) and lowest (4%) prevalence was for Tubulovesicula sp. and Carneophallus sp.
and Cholepotes sp. on Trachinocephalus myops and Parupeneus multifasciatus, respectively. Tubulovesicula
sp. on Trachinocephalus myops had a mean intensity of 22, and 1 for Bivesicula claviformis, Carneophallus
sp., Cholepotes sp., and Allobacciger diplorchis on Amphiprion perideraion, Amphiprion polymnus,
Parupeneus multifasciatus and Scolopsis taeniopterus. As an ecological and economic importance fish species,
comprehensive research on parasite infections of coral reefs can help in fisheries management and sustainable
development.
Keywords: Coral reef, marine fish, parasite, biodiversity, Vietnam
1 Institute for Biotechnology and Environment, Nha Trang University, Email: binhdangthuy@gmail.com
2 Student of Institute for Biotechnology and Environment, Nha Trang University
I. INTRODUCTION
Coral reefs are massive areas of calcium
carbonate in the oceans and are ecosystems
having high biodiversity (Vazhiyil, 2009).
Currently, the best preservation zones contain
over 700 coral species, 600 molluscs, and
nearly 4,000 fish species (Spalding et al. 2001;
Paulay, 1997). But, in fact, only about one third
of all marine fish species live on the coral reefs
(Burke et al. 2002).
Coral reef fishes are commonly traded
in the aquarium industry due to their vibrant
colors and high level of biodiversity (Alevizon,
1994). Coral reef fishes are also regarded as
food source as well as ecological resources
and tourism of more than one billion people
worldwide (UNEP, 2004; Burke et al. 2002).
Research on parasite biodiversity in coral
reefs is often neglected (Justine, 2010;
Justine et al. 2012; Justine et al. 2010;
Whittington et al. 2003; Poulin, 2004; Bouchet,
2006, Sun et al. 2012). Digenea parasites
have been reported on coastal and reef fishes
(Cribb et al. 2014; Cribb et al. 1994; Justine et
al. 2012; Jacob, 1977). In Vietnam, research
focused on zoonotic trematodes occurring on
freshwater fish has been published (Pham Cu
Thien et al. 2009; Dinh Thi Thuy et al. 2010;
Vo The Dung et al. 2008), but few studies have
examined parasite diversity on marine fishes
(Vo The Dung et al., 2008; Dang Thuy Binh et
al., 2013).
We here investigate digenean biodiversity
on common coral reef fishes in Nha Trang Bay,
Khanh Hoa Province, based on morphological
characters.
Journal of Fisheries science and Technology Special issue - 2015
24 • NHA TRANG UNIVERSITY
II. MATERIALS AND METHODS
1. Sampling
Reef fishes were collected by fishing or
purchased from fisherman at Nha Trang Bay,
Khanh Hoa Province, in 2014. A total of 116
individuals belonging to 9 species, of which
including 17 pink anemonefish (Amphiprion
perideraion), 13 saddleback clownfish
(Amphiprion polymnus), 19 yellowtail clownfish
(Amphiprion clarkii), 25 manybar goatfish
(Parupeneus multifasciatus), 4 Jenkin’s
scorpionfish (Scorpaenopsis cacopsis), 10 lattice
monocle bream (Scolopsis taeniopterus), 5
golden threadfin bream (Nemipterus hexodon),
11 snakefish (Trachinocephalus myops), and
12 variegated lizardfish (Synodus variegatus).
Fish information is presented in Table 1. Fish
were transported alive to the laboratory and
examined within 24 hrs of capture. Digeneans
were preserved in absolute alcohol (99.8%).
Table 1. Number and size of the reef fish collected in Nha Trang Bay
Coral reef fish Number (n) Length (mm) Weight (g)
Amphiprion polymnus 13 86.52 ± 51.81 30.47 ± 29.55
Amphiprion clarkii 19 68.41 ± 32.59 13.49 ± 12.51
Parupeneus multifasciatus 25 191 ± 3.4 95.92 ± 35.33
Scorpaenopsis cacopsis 4 144.5 ± 10.5 64.76 ± 15.09
Scolopsis taeniopterus 10 202.5 ± 75.5 103.01 ± 66.98
Nemipterus hexodon 5 190 ± 6 83.92 ± 12.84
Trachinocephalus myops 11 200.5 ± 55.5 77.44 ± 51.41
Synodus variegatus 12 170 ± 23 50.29 ± 16.97
Presentation value: Mean value ± Deviation
2. Species identification
Digenea parasites were collected according
to Ha Ky (2007), Cribb & Bray (2010), Bray et
al. (2011). Digenea were identified following
(Cribb et al. 1994; Justine et al. 2012; Justine
2010; Yamaguti, 1958). The morphological
features used to identify each taxa are
presented below:
Bivescula claviformis, U-shaped excretory
gland and eggs distributed into one long array.
Tetrouchetus sp., Semicircular shape,
pharynx is on the left and the yolk gland
scattered bottom body
Tubulovesicula sp. , Ventral sucker has big
size, two yolk is located in the middle of the
body, the large intestinal system and divided
into two sides
Allobacciger diplorchis, the large testes
symmetrical with 7-8 yolk distribution two sides
the body
Lecithochirium sp., Elongated body with
bulging around the ventral sucker and y-shaped
glands excrete small at the bottom body
Cholepotes sp., Elongated body, ventral
sucker nearly with oral sucker and egg
distributed mainly inside the body
Carneophallus sp., strawberry shape, two
intestine are connected together
Cainocredium labracis, the yolk gland is
distributed in whole body
3. Data analysis
3.1. Prevalence (%)
Prevalence was calculated as =
No. of infected fish
* 100
No. of examinde fish
3.2. Mean Intensity (I)
Mean intensity was calculated as =
No. of parasites
* 100
No. of infected fish
Journal of Fisheries science and Technology Special issue - 2015
NHA TRANG UNIVERSITY • 25
III. RESULTS AND DISCUSSION
1. Species identification
Seven families were represented:
Bivesiculidae (1 species Bivesicula claviformis),
Hemiuridae (2 species Lecithochirium sp., and
Tubulovesicula sp.), Botulisaccidae (1 species
Cholepotes sp.) Microphallidae (1 species
Carneohallus sp.), Monorchiidae (Allobacciger
diplorchis), Accacoeliidae (Tetrochetus sp.),
and Opecoelidae (Cainocreadium labracis).
The research detected 8 digenea species
belonging 8 genera, of which 5 species were
unidentified at the species level, because
these have many similar characteristics and
different shape, so very difficult to classify.
A list of parasites and sites of infection are
presented in Figure 1 and Table 2. Bivesicula
claviformis, and Lecithochirium sp. commonly
infect clownfishes (Amphiprion perideraion,
A. polymnus and A. aclarkii). Cainocreadium
labracis infected two fishes (Scorpaenopsis
cacopsis and Synodus variegatus). The
Figure 1. Digenea species on coral reef fish in Nha Trang Bay, Vietnam
digeneans commonly infected the gut, and
showed morphological variation regarding the
host which they infected (Fig. 1).
2. Prevalence and intensity of Digenea
species on coral reef fish
Prevalence and mean intensity was
4–63.63% and 1–22, respectively (Table
2). The highest (63.63%) and lowest (4%)
prevalences were for Tubulovesicula sp.,
Carneophallus sp. and Cholepotes sp. on
Trachinocephalus myops and Parupeneus
multifasciatus, respectively. Tubulovesicula sp.
on Trachinocephalus myops had a mean
intensity of 22 (parasite/infected fish), and 1
(parasite/infected fish) for Bivesicula claviformis,
Carneophallus sp., Cholepotes sp., and
Allobacciger diplorchis on Amphiprion perideraion,
Amphiprion polymnus, Parupeneus
multifasciatus and Scolopsis taeniopterus.
Two clown fishes and a goatfish species were
infected by 2 parasite species, the others had
been infected by 1 parasite species.
Journal of Fisheries science and Technology Special issue - 2015
26 • NHA TRANG UNIVERSITY
Research on the taxonomic diversity of
digeneans infecting marine fishes is still limited.
Presently, only crustacean have been reported
from clownfishes (Ganeshamurthy et al., 2014;
Humes, 1982; Manning, 1970; Kokshoorn,
2007; Kent, 1999; Silphaduang et al., 2000).
Tetrochetus sp. with high prevalence (>60%)
was reported on Diodon hystrix (Radhakrishnan
& Nair, 1981); Tubulovesicula sp. infects
Serranus sp. and Pomadasys olivaceum in
Karachi coast, Pakistan and the Red Sea
and Indian Ocean (Shaukat & Bilqees, 2011;
Nagaty, 1956). Cribb et al. (1994) detected 4
digeneans species belong to family Bivesiculidae
on mullets (Mugilidae). In the current study,
Tetrochetus sp., Tubulovesicula sp., Cholepotes
sp. and Carneohallus sp. infected Nemipterus
hexodon, Trachinocephalus myops, and
Parupeneus multifasciatus; whereas, Bivesicula
infected clownfish only.
Table 2. Prevalence and mean intensity of Digenea species
Host Digenean Site in host Prevalence (mean intensity)
Amphiprion perideraion Bivesicula claviformis Stomach 5.88(1)
Amphiprion polymnus
Lecithochirium sp. Stomach/Intestine 30.76(2.25)
Bivesicula claviformis Stomach 7.69(1)
Amphiprion clarkii
Bivesicula claviformis Stomach 4.26(14)
Lecithochirium sp. Stomach/Intestine 5.26(2)
Parupeneus multifasciatus
Cholepotes sp. Intestine 4(1)
Carneohallus sp. Intestine 4(1)
Scolopsis taeniopterus Allobacciger diplorchis Intestine 5.26(1)
Nemipterus hexodon Tetrochetus sp. Stomach 25(3)
Scorpaenopsis cacopsis
Cainocreadium labracis Stomach
25(6)
Synodus variegatus 8.33(2)
Trachinocephalus myops Tubulovesicula sp. Stomach/Intestine 63.63(22)
Justine (2010) surveyed parasite diversity
in New Caledonia and reported 105 parasite
species collectively representing Digenea,
Monogenea, Copepoda, Isopoda, Nematoda,
Cestoda, and Acanthocephala. Of those,
Lecithochirium sp. and Cainocreadium sp.
infected groupers (Epinephelinae), goatfishes
(Mullidae), and snappers (Lutjanidae). Justine
et al. (2012) reported 21 digeneans on 207
individual reef fish, including a species of
Lecithochirium and Allobacciger infecting
lutjanids and caesionids. The present study also
detected Lecithochirium sp. and Cainocreadium
labracis in 4 fishes (Amphiprion polymnus,
Amphiprion clarkia, Scorpaenopsis cacopsis,
and Synodus variegatus). Furthermore,
Lecithochirium sp was not found on goatfish
Parupeneus multifasciatus, while 2 other
species Cholepotes sp. and Carneohallus sp.
were discovered. The reason could be that
Parupeneus multifasciatus lives in a different
habitat, e.g. Environment contains many
phytoplankton will be infected heavily the
digenean of larva stage and flow of water also
affect to habitat as well as food souce of them,
due to make appearing the other parasite.
Cribb et al. (2000) documented the parasites
of 386 individual coral reef fish in New
Caledonia and showed that the prevalence and
intensity of digeneans is relatively low (13%
and 23, respectively). Infection status varied
according to different parasite species and
their hosts. The highest value (both prevalence
and intensity) was for Tubulovesicula sp. on
Trachinocephalus myops.
Journal of Fisheries science and Technology Special issue - 2015
NHA TRANG UNIVERSITY • 27
This is the first characterization of digenean
diversity on reef fishes in Vietnam. Clownfishes
are highly-valued ornamental fishes; whereas,
the remaining fishes are economically and
ecologically important species in Vietnam. This
information should serve as a useful baseline
with which to launch further studies into the
ecological interactions between fishes and
parasites in Vietnam.
IV. CONCLUSION
Based on morphological characteristic,
the research detected 8 digeneans species
of 8 genera, of which 6 are unidentified at the
species level. Prevalence and intensity ranged
from 4–63.63% and 1–22, respectively. The
highest (63.63%) and lowest (4%) prevalence
is for Tubulovesicula sp. and Cholepotes sp.
and Carneohallus sp., respectively. The
highest (22) and lowest (1) intensity is for
Cholepotes sp., Bivesicula claviformis,
Carneohallus sp., Allobacciger diplorchis and
Tubulovesicula sp., respectively.
ACKNOWLEDGMENT
We would like to thank EU project “Parasite
risk assessment with integrated tools in EU fish
production value chains” to provide funding
and support the implementation of this
research.
REFERENCES
1. Alevizon W. S., 1994. “Pisces Guide to Caribbean Reef Ecology” Gulf Publishing Company, ISBN
1-55992-077: 7
2. Bouchet P., 2006. The magnitude of marine biodiversity. In: C.M. Duarte (Ed.), The Exploration of Marine
Biodiversity. Scientific and Technological Challenges. Fundacion BBVA, Bilbao, pp. 31–64.
3. Bray R. A. & Justine J. L., 2011. Acanthocolpidae (Digenea) of marine fishes off New Caledonia, with the
descriptions of two new species. Folia Parasitologica, 58(1): 35–47.
4. Burke L., Reytar K., Perry A., Kushner B., Selig L., Starkhouse B., Teleki K., Waite R., Wilkinson C., Young T. &
Spalding M., 2002. Reefs at Risk in Southeast Asia. World Resource Institute, Washington DC, USA, pp. 130.
5. Cribb T. H. & Bray R. A., 2010. Gut wash, body soak, blender, and heat-fixation: approaches to the effective
collection, fixation and preservation of trematodes of fishes. Systematic Parasitology, 76: 1–7.
6. Cribb T. H., Bray R. A. & Barker S. C., 1994. Bivesiculidae and Haplosplanchnidae (Digenea) from fishes of the
southern Great Barrier Reef, Australia. Systematic Parasitology, 28: 81-97.
7. Cribb T. H., Bott N. J., Bray R. A., McNamara M. K. A., Miller T. L., Nolan M. J., Cutmore S. C., 2014.
Trematodes of the Great Barrier Reef, Australia: emerging patterns of diversity and richness in coral reef fishes.
International Journal for Parasitology: 929-939
8. Dang T. B., Vu D. H. Q., Le T. T. H., Tran Q. S., Nguyen D. K., 2013. Parasitic Metacercariae infected in fish
species based on morphological and genetic characters. Journal of Science, Can Tho University, 2: 15-23.
9. Dinh T. T., Kania P., Buchmann K., 2010. Infection status of zoonotic trematode metacercariae in Sutchi catfish
(Pangasianodon hypophthalmus) in Vietnam: Associations with season, management and host age. Aquaculture.
302(1): 19–25.
10. Ganeshamurthy R., Mohan Raj M., Sadeesh Kumar V., Veerappan N., 2014. Effect of Copepoda parasites
Caligus longipedis (Bassett-Smith in 1898) infection in marine ornamental fish Amphiprion percula and
Amphiprion clarkia. International Journal of Fisheries and Aquatic Studies 2014, 1(6): 173-175.
11. Ha & Bui, 2007. Parasite in Vietnamese freshwater fish. Science and technology Publisher, Ha Noi (in
Vietnamese), PP. 360
Journal of Fisheries science and Technology Special issue - 2015
28 • NHA TRANG UNIVERSITY
12. Justine J. L., 2010. Parasites of coral reef fish: how much do we know? With a bibliography of fish parasites in
New Caledonia. Belg. J. Zool. 140 (Suppl.): 155–190.
13. Justine J. L., Beveridge I., Boxshall G. A., Bray R. A., Miller T. L., Moravec F., Trilles J. P. & Whittington
D., 2012. An annotated list of fish parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda, Nematoda)
collected from Snappers and Bream (Lutjanidae, Nemipteridae, Caesionidae) in New Caledonia confirms high
parasite biodiversity on coral reef fish. Aquatic Biosystems : 1-29.
14. Justine J. L., Beveridge I., Boxshall G. A., Bray R. A., Moravec F., Trilles J. P. & Whittington D., 2010. An
annotated list of parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda and Nematoda) collected in
groupers (Serranidae, Epinephelinae) in New Caledonia emphasizes parasite biodiversity in coral reef fish. Folia
Parasitologica, 57(4): 237–262.
15. Kokshoorn B., 2007. Epitoniid parasites (gastropoda, caenogastropoda, epitoniidae) and their host sea anemones
(cnidaria, actiniaria, ceriantharia) in the spermonde archipelago, sulawesi, indonesia. Basteria, 71: 33-56
16. Nagaty H. F., 1956. Trematodes of fishes from the red sea. Part 6. on five distomes including one new genus and
four new species. Journal of parasitology archives.: 1-6
17. Paulay G., 1997. “Diversity and Distribution of Reef Organisms” in Life and Death of Coral Reefs, ed. Charles
Birkeland (New York: Chapman and Hall, 1997) : 303–304.
18. Pham C. T., Dalsgaard, A., Nguyen T. N.., Olsen, A., Murrell, K. D., 2009. Prevalence of zoonotic tremetode
parasites in fish fry and juveniles in fish of the Mekong Delta, Vietnam. Aquaculture, 295:1-5.
19. Poulin R., 2004. Parasite species richness in New Zealand fishes: a grossly underestimated component of
biodiversity ?. Divers. Distrib. 10: 31–37.
20. Radhakrishnan S. & Nair N. B., 1981. Tetrochetus coryphaenae (Digenea : Accacoeliidae) Infection of Diodon
hystrix (Pisces : Diodontidae). Proc. Indian natn. Sci. Acad.: 47-52
21. Silphaduang U., D.V.M., Hatai K., Ph.D., Wada S., D.V.M., Ph.D., and Noga E., M.S., D.V.M., 2000. Cladosporiosis
in a Tomato clownfish (Amphiprion frenatus). Journal of Zoo and Wildlife Medicine, 31(2): 259–261.
22. Spalding M. D., Ravilious C. & Green E. P., 2001. United Nations Environment Programme, World
Conservation Monitoring Centre. World Atlas of Coral Reefs. University of California Press: Berkeley: 416.
23. Sun D., Blomberg S. P., Cribb, T. H., McCormick M. I., Grutter A. S., 2012. The effects of parasites on the early
life stages of a damselfish. Coral Reefs, 3: 1065–1075.
24. UNEP., 2004. People and reefs, successes and challenges in the management of coral reef marine protected
areas, UNEP Regional Seas Reports and Studies No. 176, pp. 100.
25. Vazhiyil V., 2009. Marine Products for Healthcare: Functional and Bioactive Nutraceutical Compounds from the
Ocean. International Standard Book. PP. 1-552
26. Vo T. D., Murrell D., Dalsgaard A., Bristow G., Nguyen H. D., Bui N. T., Vo T. D., 2008. Prevalence of Zoonotic
Metacercariae in Two Species of Grouper, Epinephelus coioides and Epinephelus bleekeri, and Flathead Mullet,
Mugil cephalus, in Vietnam, Korean Journal of Parasitology, 46(2): 77-82.
27. Whittington I. D., Chisholm L. A., 2003. Biodiversity of marine parasites in Australia: More than just a list of
largely invisible creatures. Rec. S. Aust. Mus. Monogr. Ser. 7: 51–60.
28. Yamaguti S., 1958. Systema Helminthum. The digenetic Trematodes of vertebrates – Part II, Volume 1, PP.
1 – 1575.
Các file đính kèm theo tài liệu này:
- digenean_diversity_of_reef_fishes_in_khanh_hoa_province_viet.pdf