Research Article Volume 2 Issue 2
1Ton Duc Thang University, Vietnam
2Vietnam Meteorological and Hydrological Administration, Vietnam
Correspondence: Doan Quang Tri, Sustainable Management of Natural Resources and Environment Research Group, Faculty of Environment and Labour Safety, Ton Duc Thang University, Ho Chi Minh City, Vietnam
Received: December 04, 2017 | Published: March 28, 2018
Citation: Tri DQ, Thai TH. Biological environmental survey in Cat Ba Island. Biodiversity Int J. 2018;2(2):123–133. DOI: 10.15406/bij.2018.02.00054
Cat Ba Island has a significant biodiversity value as it is home to a number of rare and endangered species of plants and animals, with the world’s rarest primates the Golden-headed Langur. According to the study results, Cat Ba place have listed 2,380 species of animals and plants including: terrestrial plants 741 species; living animals in the forest area 282 species; mangrove plants 30 species; seaweeds 79 species; phytoplankton 287 species; plank tonic animals 98 species; sea-fish 196 species; corals 154 species. It is identified as one of the areas of highest biodiversity importance in Vietnam and is recognized as a high priority for global conservation.
Keywords: mangrove, seagrass, coral reef, phytoplankton, cat ba island
Biosphere reserves Cat Ba Island has been recognized as a UNESCO World on December 02nd, 2004. It is the 4th world’s biosphere reserve in Vietnam. Biosphere reserves Cat Ba archipelago including great majority of Cat Ba Island in Cat Hai district, Hai Phong city, Vietnam. Cat Ba Island is considered the richest marine biological system because of its diversity in the North of Vietnam. On the previous study,1 they found the Langur distribution and forest cover in Cat Ba Island (Figure 1). The objective of this study was shown the distribution of mangrove, seaweed/seagrass, coral reefs and phytoplankton in Cat Ba Island.
Description of the study area
Cat Ba is the largest of 336 islands in the Cat Ba Archipelago, and also the second largest limestone island (200 km2) in the coastal zone of Vietnam.2 It is located in the north-east of Vietnam in the northern section of the Tonkin Gulf and adjacent to Ha Long Bay (the world natural heritage site) (Figure 2). The total natural land area of Cat Ba Archipelago Biosphere Reserve is 26,240 ha, of which land area (island) is 17,040 ha and 9,200 ha of sea. Cat Ba Island is considered the richest marine biological system because of its diversity in the North of Vietnam.3‒7
Methods of field survey
Mangrove: All mangrove species that were identified in the survey sites were recorded. Also to obtain quantitative data, a 10m x 10m quadrate was set at a location that was representative of the site, and the following information was recorded: species composition, canopy height (highest and lowest), stem diameter (3 m from ground) and density (No. of stems/100 m2).
Seaweed/seagrass: All seaweed/seagrass species that were identified in the survey sites were recorded. Samples were collected and preserved in a 10% formalin solution for further analysis at IMER’s laboratory. Except sites AL11, survey was conducted only along the shoreline (underwater survey was not possible due to very low water visibility). Sites AL11 was surveyed by scuba diving.
Coral Reefs: Coral survey was conducted by squba diving at sites AL11. Species composition and live coral coverage were recorded at 5m interval along a 100 m line transect.
Phytoplankton: The qualitative Phytoplankton samples were collected by towing a plankton net (mesh size: 20μm, diameter: 20cm) several times in the vertical direction. Quantitative samples were collected from the surface by collecting 1L of surface water in the PVC bottle. All samples were preserved in 3ml Lugol solution for further analysis at IMER’s laboratory.
Demersal fish: Demersal fish was collected with a trawling net (mesh size: #15, width: 5m). Each trawl was conducted for 15 minutes at a speed of approximately 2 miles/hour. All collected species were measured (total length) and weighted, then preserved in 10% formalin solution for further analysis at IMER’s laboratory.
Diversity of the species composition
According to previous studies, a total of 2,380 species have been recorded in Cat Ba Island. Among of them 1,053 species are terrestrial species occupies 51.7% of the total species while the marine species occupies 48.3% with 985 species (Table 1). High biological diversity of the species included in the Cat Ba Island will be a very important basis for the exploitation of natural resources to serve different purposes of human. On the other hand it provides great significance in scientific research: evolution, ecology, environmental indicators along with a wide range of species likely to play an important role in the provision of ecosystem services such as disaster prevention and source of raw materials for the chemical industry and medicine production.
Taxon |
Number of species |
Taxon |
Species |
Terrestrial plant |
741 |
Zooplankton |
79 |
Terrestrial animal |
282 |
Marine fishes |
196 |
Mangrove plant |
30 |
Coral |
154 |
Phytoplankton |
287 |
Zoobenthos |
538 |
Seaweed |
79 |
|
|
|
|
Total: 2,380 species |
Table 1 The species composition recorded in Cat Ba Island8
Diversity of major marine ecosystem
Coral reefs: Coral reefs are mainly distributed at the surrounding waters in the southeast of Cat Ba Island such as Cong La, Ang Tham, Ba Trai Dao, Van Boi, Cong Hip, Tung Ngon, and Coc Cheo. The coral reefs areas are the major fishing grounds for reef fisheries due to high values of the coral reef fishes and associated reef species (Figure 3). The coral reefs in Cat Ba - Ha Long area are represented for the fringing reef types and two addition types of islands connectivity and the unofficial atoll. Generally, along the limestone islands of Cat Ba have coral distribution at a depth of 3, 6, 9 and 11 meters. Morphology of the reef is determined mainly by the morphology of the ground slopes and partly by carbonate sediments originated from organisms on the reef. Due to changes of the environmental conditions under the impact of natural and human, coral reefs are now greatly reduced in terms of area and the level of diversity of the groups living together. The percentage of the live coral coverage occupies by less than 40%, meaning classification of medium and low level by the UNESCO criteria for assessment of the coral reef health.
Figure 3Locations of the field survey sites (mangrove, seaweed/seagrass and coral reef).3 Note 1 Coral was surveyed only at sites AL11; Site AL8 was not surveyed as the area was under construction activities.
Table 2 shows the hard coral species identified through the field survey. Twenty-eight species and 58 species were identified at the sites AL11 respectively. The diversity at site AL11 was lower probably due to relatively turbid conditions. Within the identified species, 4 species are listed in the Vietnam Red Book namely: Porites lobata, Acropora aspera, Acropora formosa and Acropora nobilis; which are all classified as “Vulnerable”. Porites lobata was found at the AL11 site.
|
Survey site |
Family |
Genus/species |
Status in vietnam |
1 |
AL11 |
Acroporidae |
Acropora pulchra |
Not listed |
2 |
Poritidae |
Porites lobata |
Vulnerable |
|
3 |
Porites lutea |
Not listed |
||
4 |
Goniopora columna |
Not listed |
||
5 |
Goniopora lobata |
Not listed |
||
6 |
Agariciidae |
Pavona decussata |
Not listed |
|
7 |
Oculinidae |
Galaxea astreata |
Not listed |
|
8 |
Galaxea fascicularis |
Not listed |
||
9 |
Pectiniidae |
Pectinia lactuca |
Not listed |
|
10 |
Echinophyllia aspera |
Not listed |
||
11 |
Mycedium elephantotus |
Not listed |
||
12 |
Fungiidae |
Lithophyllon undulatum |
Not listed |
|
13 |
Sandalolitha robusta |
Not listed |
||
14 |
Mussidae |
Lobophyllia hattaii |
Not listed |
|
15 |
Lobophyllia hemprichii |
Not listed |
||
16 |
Symphyllia. agaricia |
Not listed |
||
17 |
Merulinidae |
Merulina ampliata |
Not listed |
|
18 |
Faviidae |
Favia maritime |
Not listed |
|
19 |
Favia matthaii |
Not listed |
||
20 |
Favia lizardensis |
Not listed |
||
21 |
Favia maxima |
Not listed |
||
22 |
Favites abdita |
Not listed |
||
23 |
Goniastrea pectinata |
Not listed |
||
24 |
Goniastrea favulus |
Not listed |
||
25 |
Cyphastrea serailia |
Not listed |
||
26 |
Echinopora lamellose |
Not listed |
||
27 |
Platygyra daelalea |
Not listed |
||
28 |
Dendrophylliidae |
Turbinaria peltata |
Not listed |
Table 2 List of hard coral species identified through the field survey (EIA, 2011).
Seagrass: Seagrasses are mainly distributed in Cat Ba Island in the narrow range like leopard style on tidal marshes (with the carpet of mangroves) in Gia Luan and in aquaculture ponds in Phu Long. A small area of seagrass distributes in the island of Long Chau (offshore) and Van Boi (Southeast of Cat Ba Island) where there are coral reefs with live coral cover is relatively high (Figure 4). There were only two species of seagrass have been identified in the island of Cat Ba such as Ruppia Maritima and Halophila beccarii. However, both species are not included in the Red Data Book of Vietnam, although the species of Halophila beccarii is classified at the level of “danger threatened” in the IUCN red list of threatened species, 2011.
Table 3 shows the seaweed species identified through the field survey. Seventeen species belonging to 9 families were identified. Chaetomorpha capillaris and Enteromorpha compressa were the most common species. Some species such as Asparagopsis taxiformis, Colpomenia sinuosa, and Cladophoropsis membrannacea were identified at only specific sites. None of the identified species are included in the Vietnam Red Book. Some species in the Ulvaceae family are harvested for food stuffs in certain areas of Vietnam. Table 2 shows the seagrass species identified through the field survey. Only two seagrass species Ruppia maritima and Halophila beccarii were identified, which were found at sites AL10 and AL11 respectively. Halophila beccarii was record for the first time in the surveyed area. Although both species are not included in the Vietnam Red Book, Halophila beccarii is classified as “Vulnerable” in IUCN Red List.
|
Family |
Genus/species |
Status in vietnam red book |
Identified survey sites |
1 |
Ceramiaceae |
Bostrychia binderi |
Not listed |
AL3, AL5, AL7, AL10 |
2 |
Polysiphonia sertularioides |
Not listed |
AL1, AL2, AL10 |
|
3 |
Delesseriaceae |
Caloglosa ogasawaraensis |
Not listed |
AL2, AL3, AL7 |
4 |
Dictyotaceae |
Padina australis |
Not listed |
AL11 |
5 |
Cladophoraceae |
Chaetomorpha capillaris |
Not listed |
AL1, AL03, AL5, AL7, AL10, AL11 |
6 |
Ch. linum |
Not listed |
AL1, AL10 |
|
7 |
E. compressa |
Not listed |
AL1, AL3, AL5, AL7, AL10, AL11 |
|
8 |
E. kylinii |
Not listed |
AL1, AL10 |
|
9 |
E. flexuosa |
Not listed |
AL1 |
|
10 |
Ulva conglobata |
Not listed |
AL5 |
|
11 |
Ruppiaceae |
Ruppia maritima |
Not listed |
AL10 |
12 |
Hydrocharitaceae |
Halophila beccarii |
Not listed |
AL11 |
Table 3 List of seaweed species identified through the field survey (EIA, 2011).
Mangrove forest: The mangrove forest and the coral reefs are the invaluable natural resources of the tropical countries in general and Cat Ba in particular. They play as the sources of genetic reservation, increasing of the natural biomass and stabilization for the shoreline. Most of the mangrove forests maintain high cover in the western side of Cat Ba Island (Phu Long Natural Reserve). In near future, the fight campaign for climate change will lean much on these green corridors (Figure 5).
Most of the mangrove areas distribute in Phu Long Commune with high relative density. The total area is 775.98 ha of mangrove forest is divided into two types: mangrove distribution outside the farming area (224.74 ha), mangrove distribution in ponds (551.24 ha) (Figure 6). Because mangrove forests in farming systems are relatively large so the long-term master plan and conservation of mangroves will be difficult due to satisfactorily resolve the relationship of private-public ownership. Table 4 shows the mangrove species identified through the field survey. Eleven species belonging to 9 families were identified. Rhizophora stylosa and Avicennia marina were the most common species in the survey area. None of the identified species are included in the Vietnam Red Book.
No. |
Family |
Genus/species |
Status in vietnam |
Identified survey sites |
1 |
Sonneratiaceae |
Sonneratia caseolaris |
Not listed |
AL10 |
2 |
Rhizophoraceae |
Rhizophora stylosa |
Not listed |
AL1, AL2, AL3, AL5, AL7 |
3 |
Kandelia obovata |
Not listed |
AL5, AL10 |
|
4 |
Bruguirea gymnorrhiza |
Not listed |
AL1, AL3, AL7 |
|
5 |
Aviceniaceae |
Avicennia marina |
Not listed |
AL1, AL2, AL3, AL5, AL7 |
6 |
Myrsinaceae |
Aegiceras corniculatum |
Not listed |
AL1, AL3 |
7 |
Pteridaceae |
Acrostichum aureumh |
Not listed |
AL10 |
8 |
Verbenaceae |
Cleodendrum inerme |
Not listed |
AL2, AL10 |
9 |
Euphorbiaceae |
Excoecaria agallocha |
Not listed |
AL3, AL5 |
10 |
Malvaceae |
Hibiscus tiliaceus |
Not listed |
AL5 |
Table 4 List of mangrove species identified through the field survey.
Phytoplankton: Phytoplanktons are the keystone species in this habitat type, providing basic food items for the zoobenthis and fish that are the key targets of the capture fishery (Figure 7). Table 5 and Table 6 show the phytoplankton species identified through the dry and wet season surveys respectively. In the dry season, a total of 134 species were identified (Table 5). The genus Chaetoceros was found in many survey sites, which play an important role as food sources for fish and other marine species, in particular at the early stages of their life cycle. Some of the identified dinoflagellate species such as Ceratium fusus, Prorocentrum micans and Dinophysis caudate are known to cause red tide and harmful algae bloom when at high density. In the rainy season, a total of 136 species were identified (Table 6). The density of the phytoplankton has been driven by some dominante species such as Skeletonema costatum with the cell density is approximate 103 up to 4,104 cell/L; next to the Chaetoceros spp. with the density from 103 - 56,103 cell/L; Ceratium furca has the density from 2.103 to approximate of 104 cell/L (EC9 site); Oscillatoria sp.2 103 cell/L and Bacteriastrum spp. reaches 47,103 cell/L.
Figure 7Locations of the field survey sites (phytoplankton, zooplankton, zoobenthos, demersal fish and other zoobenthos).3
Table 5 to Table 6 shows the number of phytoplankton species and cell density at each survey site. For the dry season, the number of species ranged between 32 and 57 species. While there was no clear spatial trend in the cell density, relatively high levels were recorded at the EC4 and EC8 sites. The seasonal variation shows a clearly trend of reduction both interm of species composition and cell density. However, the number of species is slightly lower in rainy season while the cell density rapidly reduces up to 98.42% at the EC8 site to 22.3% at the EC11 site.
No. |
Scientific name |
No. of identified survey sites |
No. |
Scientific name |
No. of identified survey sites |
No. |
Scientific name |
No. of identified survey sites |
No. |
Scientific name |
Phylum- Bacillariophyceae |
Phylum- Bacillariophyceae |
Phylum - Dinophyceae |
Phylum - Dinophyceae |
|||||||
1 |
Paralia sulcata |
1 |
42 |
Chaetoceros lorenzianus |
11 |
83 |
Ceratium macroceros |
4 |
124 |
Pyrophacus horologicum |
2 |
Hyalodiscus stelliger |
1 |
43 |
Chaetoceros paradoxus |
3 |
84 |
Ceratium massiliense |
4 |
Phylum - Dictyochophyceae |
|
3 |
Cyclotella striata |
3 |
44 |
Chaetoceros rostratus |
9 |
85 |
Ceratium asymmetricum |
2 |
125 |
Dictyocha fibula |
4 |
Cyclotella comta |
6 |
45 |
Chaetoceros subtilis |
3 |
86 |
Ceratium tripos |
3 |
126 |
Dictyocha speculum |
5 |
Cyclotella sp. |
1 |
46 |
Biddulphia regia |
2 |
87 |
Prorocentrum micans |
10 |
Phylum - Cyanophyceae |
|
Phylum- Bacillariophyceae |
47 |
Biddulphia reticulum |
3 |
88 |
Prorocentrum rhathymum |
1 |
127 |
Trichodesmium erythraeum |
||
6 |
Coscinodiscus asteromphalus |
12 |
48 |
Odontella mobiliensis |
1 |
89 |
Prorocentrum sp. |
2 |
128 |
Oscillatoria sp. |
7 |
Coscinodiscus oculus-iridis |
6 |
49 |
Hemiaulus sinensis |
1 |
90 |
Dinophysis caudata |
10 |
Phylum – Chlorophyceae |
|
8 |
Coscinodiscus radiatus |
1 |
50 |
Cerataulina bergonii |
1 |
91 |
Dinophysis mitra |
1 |
129 |
Pediastrum simplex v. simplex |
9 |
Coscinodiscus granii |
1 |
51 |
Cerataulina compacta |
1 |
92 |
Dinophysis cf. rotundata |
1 |
130 |
Pediastrum duplex v. duplex |
10 |
Coscinodiscus cf. subtilis |
3 |
52 |
Ditylum brightwellii |
1 |
93 |
Noctiluca scintillans |
4 |
131 |
Pediastrum sp. |
11 |
Coscinodiscus sp. |
1 |
53 |
Eucampia zoodiacus |
6 |
94 |
Gonyaulax sp. |
4 |
132 |
Scenedesmus sp. |
12 |
Lauderia borealis |
5 |
54 |
Climacodium biconcavum |
3 |
95 |
Gonyaulax polygramma |
9 |
133 |
Scenedesmus quadricauda |
13 |
Skeletonema costatum |
8 |
55 |
Palmeria hardmaniana |
5 |
96 |
Gonyaulax spinifera |
1 |
134 |
Staurastrum sp. |
14 |
Leptocylindrus danicus |
3 |
56 |
Thalassionema frauenfeldii |
12 |
97 |
Gonyaulax scrippsae |
2 |
|
|
15 |
Guinardia flaccida |
8 |
57 |
Navicula membranacea |
7 |
98 |
Gonyaulax verior |
1 |
|
|
16 |
Guinardia striata |
12 |
58 |
Navicula cancellata |
2 |
99 |
Gonyaulax rotundata |
2 |
|
|
17 |
Bacteriastrum varians |
5 |
59 |
Tropidoneis lepidoptera |
1 |
100 |
Gonyaulax diegiensis |
4 |
|
|
18 |
Bacteriastrum hyalinum |
5 |
60 |
Pleurosigma affine |
4 |
101 |
Protoperidinium steinii |
5 |
|
|
19 |
Thalassiosira eccentrica |
2 |
61 |
Pleurosigma angulatum |
1 |
102 |
Protoperidinium conicum |
10 |
|
|
20 |
Thalassiosira lineata |
6 |
62 |
Pleurosigma sp.1 |
7 |
103 |
Protoperidinium crassipes |
8 |
|
|
21 |
Thalassiosira sp. |
2 |
63 |
Pleurosigma sp.2 |
1 |
104 |
Protoperidinium divergens |
6 |
|
|
22 |
Arthrospira platensis |
2 |
64 |
Pleurosigma naviculaceum |
4 |
105 |
Protoperidinium depressum |
1 |
|
|
23 |
Rhizosolenia robusta |
3 |
65 |
Pleurosigma pelagicum |
4 |
106 |
Protoperidinium elegans |
3 |
|
|
24 |
Rhizosolenia setigera |
2 |
66 |
Amphiprora alata |
1 |
107 |
Protoperidinium oceanicum |
3 |
|
|
25 |
Rhizosolenia hyalina |
4 |
67 |
Nitzschia lorenziana |
6 |
108 |
Protoperidinium ovum |
9 |
|
|
26 |
Proboscia alata |
9 |
68 |
Nitzschia longissima |
2 |
109 |
Protoperidinium pellucidum |
11 |
|
|
27 |
Proboscia alata f. indica |
1 |
69 |
Nitzschia longissima v. reversa |
1 |
110 |
Protoperidinium pentagonum |
1 |
|
|
28 |
Proboscia alata f. gracillima |
1 |
70 |
Nitzschia sigma |
4 |
111 |
Protoperidinium leonis |
2 |
|
|
29 |
Proboscia alata f. genuina |
1 |
71 |
Nitzschia sigma v. intercedens |
1 |
112 |
Protoperidinium spinulosum |
1 |
|
|
30 |
Chaetoceros affinis |
12 |
72 |
Pseudonitzschia sp.1 |
8 |
113 |
Protoperidinium sphaeroides |
6 |
|
|
31 |
Chaetoceros affinis v. willei |
1 |
73 |
Pseudonitzschia sp.2 |
2 |
Phylum - Dinophyceae |
|
|
||
32 |
Chaetoceros abnormis |
5 |
74 |
Surirella ovalis |
5 |
114 |
Protoperidinium sp. |
8 |
|
|
33 |
Chaetoceros curvisetus |
4 |
75 |
Surirella gemma |
2 |
115 |
Peridinium quinquecorne |
2 |
|
|
34 |
Chaetoceros compactus |
3 |
76 |
Campylodiscus echeneis |
3 |
116 |
Scrippsiella sp. |
1 |
|
|
35 |
Chaetoceros compressus |
7 |
77 |
Campylodiscus undulatus |
1 |
117 |
Alexandrium sp. |
2 |
|
|
36 |
Chaetoceros constrictus |
12 |
Phylum - Dinophyceae |
118 |
Alexandrium pseudogonyaulax |
4 |
|
|
||
37 |
Chaetoceros decipiens |
1 |
78 |
Ceratium breve |
3 |
119 |
Goniodoma polyedricum |
5 |
|
|
38 |
Chaetoceros denticulatus |
3 |
79 |
Ceratium furca |
11 |
120 |
Diplopsalis sp. |
5 |
|
|
39 |
Chaetoceros distans |
2 |
80 |
Ceratium deflexum |
2 |
121 |
Diplopsalopsis sp. |
2 |
|
|
40 |
Chaetoceros dydimus |
1 |
81 |
Ceratium fusus |
11 |
122 |
Zygabikodinium sp. |
1 |
|
|
41 |
Chaetoceros lauderii |
1 |
82 |
Ceratium trichoceros |
10 |
123 |
Oblea sp. |
2 |
|
|
Table 5 List of phytoplankton species identified through the field survey (in dry season)
No. |
Scientific name |
No. of identified survey sites |
No. |
Scientific name |
No. of identified survey sites |
No. |
Scientific name |
No. of identified survey sites |
|
Bacillariophyceae (Diatoms) |
Bacillariophyceae (Diatoms) |
Bacillariophyceae (Diatoms) |
|||||||
1 |
Paralia sulcata |
2 |
46 |
Eucampia cornuta |
1 |
91 |
Protoperidinium pellucidum |
6 |
|
2 |
Melosira granulata |
2 |
47 |
Eucampia zoodiacus |
2 |
92 |
Protoperidinium pentagonum |
2 |
|
3 |
Melosira granulata v. angustissima |
6 |
48 |
Climacodium biconcavum |
1 |
93 |
Protoperidinium punctulatum |
1 |
|
4 |
Cyclotella comta |
11 |
49 |
Palmeria hardmaniana |
4 |
94 |
Protoperidinium spinulosum |
6 |
|
5 |
Coscinodiscus asteromphalus |
11 |
50 |
Thalassionema nitzschioides |
5 |
95 |
Protoperidinium sphaeroides |
1 |
|
6 |
Coscinodiscus oculus-iridis |
4 |
51 |
Thalassionema frauenfeldii |
11 |
96 |
Protoperidinium sp. |
1 |
|
7 |
Coscinodiscus jonesianus |
1 |
52 |
Pleurosigma affine |
2 |
97 |
Protoperidinium sp.1 |
2 |
|
8 |
Coscinodiscus jonesianus v. commutata |
12 |
53 |
Pleurosigma sp. |
2 |
98 |
Peridinium sp. |
1 |
|
Bacillariophyceae (Diatoms) |
54 |
Pleurosigma sp.1 |
1 |
99 |
Alexandrium sp. |
1 |
|||
9 |
Coscinodiscus marginatus |
1 |
55 |
Nitzschia lorenziana |
3 |
100 |
Goniodoma polyedricum |
1 |
|
10 |
Coscinodiscus cf. subtilis |
1 |
56 |
Nitzschia longissima |
1 |
101 |
Lingulodinium polyedra |
5 |
|
11 |
Asteromphalus cleveanus |
1 |
57 |
Pseudo-nitzschia sp.1 (P. cf. pungens ) |
3 |
102 |
Diplopsalis sp. |
2 |
|
12 |
Thalassiosira eccentrica |
3 |
58 |
Campylodiscus echeneis |
1 |
103 |
Diplopsalopsis sp. |
2 |
|
13 |
Thalassiosira lineata |
12 |
59 |
Ceratium breve |
2 |
104 |
Zygabikodinium sp. |
1 |
|
14 |
Thalassiosira sp. |
2 |
60 |
Ceratium deflexum |
1 |
105 |
Pyrophacus horologium |
1 |
|
15 |
Lauderia borealis |
11 |
61 |
Ceratium extensum |
1 |
106 |
Pyrophacus sp. |
7 |
|
16 |
Skeletonema costatum |
11 |
62 |
Ceratium falcatum |
1 |
107 |
Podolampas bipes |
1 |
|
17 |
Guinardia flaccida |
5 |
63 |
Ceratium furca |
11 |
Cyanophyceae (Cyanobacteria) |
|||
18 |
Guinardia striata |
2 |
64 |
Ceratium fusus |
4 |
108 |
Trichodesmium erythraeum |
2 |
|
19 |
Dactyliosolen mediterraneus |
2 |
65 |
Ceratium trichoceros |
6 |
109 |
Oscillatoria limosa |
3 |
|
20 |
Bacteriastrum varians |
8 |
66 |
Ceratium massiliense |
1 |
110 |
Oscillatoria raciborskii |
3 |
|
21 |
Bacteriastrum hyalinum |
1 |
67 |
Ceratium tripos |
3 |
111 |
Oscillatoria sp.1 |
6 |
|
22 |
Pseudosolenia calcar-avis |
3 |
68 |
Ceratium sp. |
1 |
112 |
Oscillatoria sp.2 |
2 |
|
23 |
Rhizosolenia cylindrus |
1 |
69 |
Dinophysis miles |
3 |
113 |
Oscillatori princeps |
2 |
|
24 |
Rhizosolenia robusta |
1 |
70 |
Dinophysis caudata |
11 |
114 |
Lyngbya sp. |
1 |
|
25 |
Chaetoceros affinis |
8 |
71 |
Dinophysis hastata |
1 |
115 |
Arthrospira platensis |
9 |
|
26 |
Chaetoceros abnormis |
5 |
72 |
Dinophysis doryphorum |
1 |
116 |
Anabaena sp. |
4 |
|
27 |
Chaetoceros curvisetus |
10 |
73 |
Dinophysis sp. |
1 |
117 |
Anabaena cf. viguieri |
1 |
|
28 |
Chaetoceros coarctatus |
2 |
74 |
Ornithocercus magnificus |
1 |
118 |
Microcystis cf. wesenbergii |
7 |
|
29 |
Chaetoceros compressus |
3 |
75 |
Histioneis costata |
1 |
119 |
Microcystis sp. |
7 |
|
30 |
Chaetoceros constrictus |
2 |
76 |
Amphisolenia bidentata |
3 |
Chlorophyceae (Chlorophyte) |
|||
31 |
Chaetoceros crinitus |
1 |
77 |
Gymnodinium sanguineum |
1 |
120 |
Pediastrum simplex v. simplex |
9 |
|
32 |
Chaetoceros diversus |
3 |
78 |
Gonyaulax sp. |
3 |
121 |
Pediastrum boryanum v. boryanum |
1 |
|
33 |
Chaetoceros distans |
1 |
79 |
Gonyaulax polygramma |
3 |
122 |
Pediastrum duplex v. duplex |
8 |
|
34 |
Chaetoceros lorenzianus |
7 |
80 |
Gonyaulax rotundata |
5 |
123 |
Pediastrum sp. |
3 |
|
35 |
Chaetoceros subtilis |
9 |
81 |
Protoperidinium abei |
1 |
124 |
Pediastrum tetras |
4 |
|
36 |
Biddulphia regia |
11 |
82 |
Protoperidinium cf. brochii |
3 |
125 |
Scenedesmus sp. |
3 |
|
37 |
Biddulphia dubia |
1 |
Bacillariophyceae (Diatoms) |
126 |
Scenedesmus quadricauda |
6 |
|||
38 |
Biddulphia reticulum |
1 |
83 |
Protoperidinium conicum |
11 |
127 |
Scenedesmus carinatus |
1 |
|
39 |
Odontella mobiliensis |
4 |
84 |
Protoperidinium claudicans |
4 |
128 |
Scenedesmus acuminatus var. acumin |
1 |
|
40 |
Bellerochea horologicalis |
1 |
85 |
Protoperidinium crassipes |
3 |
129 |
Scenedesmus javanensis |
2 |
|
41 |
Hemiaulus sinensis |
3 |
86 |
Protoperidinium divergens |
1 |
130 |
Staurastrum sp. |
8 |
|
42 |
Hemiaulus indicus |
1 |
87 |
Protoperidinium elegans |
1 |
131 |
Palmella sp. |
1 |
|
43 |
Cerataulina bergonii |
1 |
88 |
Protoperidinium oceanicum |
6 |
132 |
Eudorina elegans |
1 |
|
44 |
Cerataulina compacta |
1 |
89 |
Protoperidinium ovum |
1 |
133 |
Eudorina sp. |
4 |
|
45 |
Ditylum sol |
11 |
90 |
Protoperidinium thorianum |
1 |
|
|
|
Table 6 List of phytoplankton species identified through the field survey (in rainy season)
Demersal fish: Table 7 shows the demersal fish species identified through the dry and rainy season surveys respectively. In the dry season, in general, fish diversity and abundance were significantly higher in the shallow coastal survey sites (e.g. EC1, EC2, EC4, and EC7) compared to the deeper offshore survey sites. Within the identified species, two species are listed in Vietnam Red Book namely, Bostrichthys sinensis and Anodontostoma chacunda, which were found in the shallow coastal survey sites EC1 and EC2 respectively. Bostrichthys sinensis and Anodontostoma chacunda are classified as “Critical” and “Vulnerable” respectively. In the wet season, the similar trend in term of fish diversity and abundance has been found among sampling sites (shallow sites are more abundance than the off shore sites). However there are differences in the species composition of the economic species with the distribution of the family Sciaenidae to occur in 9/11 sampling sites. This family also contributes for higher biomass of the total catch at the sampling sites of EC8, EC9 in the rainy survey.
Survey site |
Family |
Genus/species |
No. of individuals |
Total and ave. wet weight (g) |
Average length (cm) |
Status in vietnam red book |
In dry season |
||||||
EC1 |
Sparidae |
Sparus latus |
1 |
6 |
6.5 |
Not listed |
Taenioididae |
Trypauchen |
2 |
Total: 12.97 |
9 |
Not listed |
|
vagina |
Ave. : 6.5 |
|
||||
Eleotridae |
Bostrichthys |
1 |
23 |
13 |
Critical |
|
sinensis |
||||||
Sillaginidae |
Sillago sihama |
1 |
15.4 |
12.5 |
Not listed |
|
Eleotridae |
Butis butis |
1 |
4.5 |
5 |
Not listed |
|
Platycephalidae |
Rogadus asper |
1 |
12.5 |
11 |
Not listed |
|
Platycephalidae |
Cociella |
1 |
5 |
5.5 |
Not listed |
|
crocodila |
||||||
Cynoglossidae |
Symphurus |
1 |
4.5 |
3.5 |
Not listed |
|
orientalis |
||||||
EC2 |
Cynoglossidae |
Symphurus |
1 |
11 |
9.5 |
Not listed |
orientalis |
||||||
Soleidae |
Heteromycterus |
1 |
13 |
8 |
Not listed |
|
japonica |
||||||
Sillaginidae |
Sillago sihama |
1 |
12.5 |
14.9 |
Not listed |
|
Clupeidae |
Anodontostoma |
5 |
Total: 60 |
15.3 |
Vulnerable |
|
chacunda |
Ave: 12 |
|||||
Sciaenidae |
Nibea albiflora |
1 |
26 |
23.5 |
Not listed |
|
In rainy season |
||||||
EC1 |
Muraenesocidae |
Muraenesox |
1 |
36 |
25 |
Not listed |
cinereus |
||||||
Taenioididae |
Trypauchen |
2 |
Total: 25.4 |
13 |
Not listed |
|
vagina |
Ave. : 12.7 |
|||||
Eleotridae |
Bostrichthys |
1 |
Total: 42 |
12.5 |
Critical |
|
sinensis |
Ave: 14 |
|||||
Sciaenidae |
Nibea soldado |
26 |
Total: 93.37 |
7.2 |
Not listed |
|
Ave: 3.59 |
||||||
Siganidae |
Siganus |
1 |
7.5 |
8 |
Not listed |
|
fuscescens |
||||||
EC2 |
Bagridae |
Cranoglanis |
9 |
Total: 400 |
22.3 |
Not listed |
sinensis |
Ave: 44.4 |
|||||
Bothidae |
Arnoglossus |
3 |
Total: 3.13 |
5 |
Not listed |
|
tenuis |
Ave: 1.04 |
|||||
Clupeidae |
Anodontostoma |
2 |
Total: 30 |
16.7 |
Vulnerable |
|
chacunda |
Ave: 15 |
|||||
Sciaenidae |
Nibea albiflora |
3 |
Total: 17.04 |
3.5 |
Not listed |
|
Ave: 5.68 |
Table 7 Results of demersal fish survey
Diversity of terrestrial animals
Cat Ba National Park is tropical moist forest on limestone, which harbors a number of endemic and rare species, foremost of which is the endemic Cat Ba Langur Trachypithecus poliocephalus poliocephalus.9‒11 These led to the discovery of new species of Goniurosaurus12 (Figure 8) and Sphenomorphus.13 Among the 40 reptile species recorded from Cat Ba Island, two species are listed in the IUCN Red List (2008), seven species are listed in the Vietnam Red Data Book,14 four in the CITES appendices (2008), and five species are protected by governmental law (Decree No. 32/2006/ND-CP) (Table 8).
Figure 8(1) Cuora mouhotii¬. (2) Acanthosaura lepidogaster. (3) Pseudocalotes brevipes. (4) Goniurosaurus catbaensis. (5) Gekko gecko. (6) Gekko palmatus. (7) Hemidactylus frenatus. (8) H garnotii. (9) Eutropis multifasciatus. (10) Plestiodon quadrilineatus. (11) Scincella reevesii. (12) Sphenomorphus tonkinensis.12
Scientific name |
IUCN |
VNRB |
CITES |
Dec. 32 |
2008 |
2007 |
2008 |
2006 |
|
Physignathus cocincinus |
|
VU |
|
|
Gekko gecko |
|
VU |
|
|
[Varanus salvator] |
|
EN |
II |
IIB |
[Python molurus] |
LR/nt |
CR |
I |
IIB |
Coelognathus radiatus |
|
EN |
|
IIB |
Ptyas korros |
|
EN |
|
|
Bungarus multicinctus |
|
|
|
IIB |
Naja atra |
|
EN |
II |
IIB |
Cuora mouhotii |
EN |
|
II |
|
Table 8 List of threatened reptile species recorded from Cat Ba Island13
Notes: IUCN: IUCN Red List, VNRB: Vietnam Red Data Book: CR: critically endangered, EN: endangered, VU: vulnerable, LR/nt: near threatened; CITES: I, II = Appendix I and II; Dec. 32: Governmental Decree No. 32/2006/ND-CP: IB = Group IB (prohibited exploitation and use for commercial purpose), IIB = Group IIB (limited exploitation and use for commercial purpose); []: Only photographic record or observation.
In this study, there are occurrences of three main key habitats: mangrove, coral reefs, and seaweeds/seagrass. These contribute for species diversity and abundance of the natural marine resources available for the local people to exploit. The distribution trends of the living resources are higher abundance in the near shore sites, lower abundance at the offshore sites. These may relate to the biological/physical driven factors such as the available of substrate/habitat, natural food resources or water current. The coastal sites provide the nursery grounds for the economic species where the mangrove forests remain as the shelters.
We would like to thank the National Hydro-meteorological Service (NHMS) for their assistance in the collection of topography map and data for this paper. We are thankful to the NHMS for this research opportunity and providing permission for using their facilities to perform the study.
The authors declare that there are no competing interests regarding the publication of this paper.
©2018 Tri, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.