µ
Nanoplankton Distribution and Abundance in the Vietnamese Waters of the South China Sea
Lokman Shamsudin, Kartini Mohamad, S. Noraslizan and M. Kasina Faculty of Science & Technology, Universiti Putra Malaysia Terengganu,
Mengabang Telipot, 21030 Kuala Terengganu, Malaysia
ABSTRACT
A collaborative sea cruise in the Vietnam waters of the South China Sea was conducted in the postmonsoon (21 April to 5 June, 1999) period on board MV SEAFDEC. The nanoplankton from 21 sampling stations consisted of 134 taxa comprising predominantly of centric nanodiatom (29 species), pennata nanodiatom (40 species) and dinoflagellate (65 species). Among the minute plankton collected, three species of nanodiatom (Minidiscus comicus, M. chilensis, M. trioculatus) and numerous dinoflagellate species were present. The pennate nanodiatom comprised of the species of Asterionella, Psammodiscus and Amphipleura ranging from 5.25 x 102 to 1.67 x 104 cell/L; all which were <20µm in size. The dominant centric nanodiatom comprised of species of Thalassiosira, Minidiscus, Chaetoceros and Cyclotella, ranging from 1.36 x 102 to 4.61 x 104 cell/L. The genera of Chaetoceros, Minidiscus, Cyclotella, Coscinodiscus, Navicula, Fragilaria and Thalassiosira contained a wide range of species; however, majority of these species were new records and have not been taxonomically identified. The Prymnesiophyta (mostly small flagellate cells and Prasinophyta species) were rarely present; while those of dinoflagellate consisted of a wide range of species of genera Amphidoma, Centrodinium, Palaephalacroma, Peridinum, Planodinium, Gyrodinium, Gonyaulax, Scrippsiella, Protoperidinium and Protocentrum. The genera of Protoperidinium, Peridinium, Gonyaulax and Prorocentrum had a wide range of species. The class Heptophyceae comprising of Prymnesiaceae, Coccolithaceae and Gephyrocapsaceae were rarely present. The total nanoplankton population (ranging from 0.24 x 104 to 5.47 x 104 L-1) was dense in nearshore regions (especially in waters between Da Nang and Nha Trang) and tend to spread out in concentric semicircle into the open sea. The presence of the dinoflagellate species of Amphidoma, Centradinium and Planadinium were detected in considerable amounts at midshore Vietnam waters of the South China Sea. Blooms of Gyrodonium sp. and Amphidoma sp. (to a limited extend) occurred during the study period.
Key words: algae, dinoflagellate, nanoplankton, Vietnam, South China Sea
Introduction
For the past many years, the nanoplankton study has not been emphasised or given priority due its minute size (<20 m) and difficulty in identifying; however, this should not lead to its reglect since in many waters it is responsible for more than 50% biomass carbon fixation and production in the ocean than the more immediate microplankton whose size is much bigger ( 20 to 200 µm) Only a few studies of plankton (especially the minute nanoplankton) and other related parameters were carried out on the Malaysian waters in the South China Sea. Chua and Chong (1973) showed that the distribution and abundance of pelagic species especially the small tuna (Euthynus affinis), chub mackerel (Rastrelliger sp.) and anchovies (Stolephorus sp.) were related to the density of phytoplankton.
Qualitative studies of microplankton (20-200 µm in size) in the Malaysian coastal waters, especially the Malacca Straits have been conducted by Sewell (1933), Wickstead (1961) and Pathansali (1968). Primary productivity in the same location had been carried out by Doty et al. (1963); however, a detailed study of the nanoplankton community structure, distribution and abundance in such waters had been lacking. Studies by Shamsudin et al. (1987) in the South China Sea around coasts of Johore, Terengganu and Kelantan found that majority of the phytoplankton found were diatoms which comprised of numerous species of Bacteriastrum, Chaetoceros, Rhizosolenia and Pleurosigma. The blue green, Trichodesmium erythraeum was found in abundance in such tropical waters (Chua & Chong, 1973). Studied on plankton (Shamsudin, 1987; Shamsudin & Baker, 1987; Shamsudin et al., 1987;
Semina, 1967; Markina, 1972) had raised questions about the qualitative and quantitative seasonal availability of these organisms as sources of food for those organisms higher up in the food chain and the relative production of these organisms in various study sectors of the South China Sea.
In the present study, the nanoplankton community structure has been analysed during the postmonsoon study period (April/June 1999) in the Vietnam waters of the South China Sea. The species community structure patterns, distribution, composition and species abundance at various study sectors of the South China Sea had been highlighted and emphasized in this study.
Materials and Methods Study Area
The study area (Fig. 1) covers an area which extends from the northern tip of Vietnam (21o 0’
N; 107o 55’ E) to the south west covering the Mekong Delta (9o 0.1’ N; 104o 30.5’ E) of the South China Sea. The estimated study area is ca 6000 nautical square miles (ca 2000 sq. km) covering the economic exclusive zone (EEZ) of the Vietnam waters of the South China Sea. The sea cruise track followed a zig-zag manner starting from the northern coastal Vietnam waters and ended up at the southern end of the Vietnam waters (facing the Mekong Data) covering a total of 21 sampling stations.
The Gulf of Tongking and the Hainan Dao island are situated in the north of the Vietnam waters while the Paracel island and Spratly island to the south of Hainan Dao island. The Mekong river delta is at the southern tip of Vietnam, while the Song Pa river with its river tributaries passing through Hai Phong.
Sampling Method & Preparation
The research survey was carried out during the cruise survey in April/June 1999 covering twenty one stations. Water sampler (twin 10 L sampler) was used to collect water sample from the depth of the maximum chlorophyll layer (MCL). The water sampel was first filtered through the 40 µm mesh-size filtering net; it was again subsequently filtered through a membrane filter paper (0.8 µm mesh-size) with square grid marks on its surface. The samples which had been fixed and preserved in absolute alcohol, were then mounted on (SEM) stubs with double-sided cellotape. The stubs with adhering samples were then coated with an alloy (gold with pelladium) before being observed under the scanning electron microscope (Barber & Haworth, 1981). For each stub, only 5 square grids (one grid having 20 fields of observation; one field measures 32.5 x 25 µm area) were considered whereby the organisms found on the grid were countered. The subsamples or subportions of original sample were preserved in 10% formalin and subsequently examined for species composition and abundance using an inverted microscope (Vollenweider et al., 1974; Tippett, 1970; Shamsudin, 1987, 1993, 1994, 1995; Shamsudin & Shazili, 1991; Shamsudin & Sleigh, 1993, 1995; Shamsudin et al., 1987, 1997). Algal were identified with reference to Okada and McIntyre (1977), Gaardnar and Heindel (1978) and Heimdal and Gaarder (1980, 1981).
1
5
9 1 1 1 4 1 5 1 6
1 9 1 7 2 0
2 2 2 4
2 7 2 9 3 8
5 0 4 2 5 2 5 5
5 7 5 8
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
Longitude
Latitude CHINA VIETNAM
THAILAND
CAMBODIA
Statistical Analysis
An index of the composition of the plankton community in the aquatic habitat is given by calculating the diversity index (H) and evenness (J) of the community structure using the Shannon-Weiner index (1949). The formula for calculating Shannon-Weiner (diversity) index (H) is:
H = Pi log2 Pi , Where Pi = ni/N
ni = The number of individuals of the i th species N = The total number of individuals
The diversity index can measure species richness (H) and species evenness (J)
J = H/log2 S - (ii), S is the number of species
One way analysis of variance can be imployed when comparisons are made between a number of independent random samples, one sample from each population. All counts must be classified in the same manner, but the number of counts in the various samples can be different (Elliott, 1977). Analysis of variance can be used to assess the relative importance of different sources of variation, e.g. between sites, between dates, etc., but it may be necessary to transform the data before analysis of variance tests are applied.
Coefficients of similarity are simple measures of the extent to which two habitats have species (or individuals) in common (Southwood, 1978). Essentially, such coefficient can be of two types, as given below, and both types reflect the similarity in individuals between the habitats.
Fig. 1. The map showing the sampling stations in the Vietnam waters of the South China Sea (cruise April-June 1999).
(i) JaccardCj = j / (a + b-j)
(ii) Sorensen Cs = 2j / (a+b)
where a, b are the total individuals sampled in habitat a and b respectively, and j is the sum of the lesser values for the species common to both habitats (Southwood, 1978). In habitats where one or few species have high dominance the coefficients under-estimate the contributions of the moderately common species which may be more stable indicators of the characteristic fauna of an area while the rare species have little impacts (Southwood, 1978). It is apparent that Cs is greater than Cj and the inequality reduces as j approaches the magnitude of 1/2 (a+b).
The microplankton can be classified into species assemblages or associations in cluster analysis on species sampled from the nearshore and offshore stations according to their preference on environmental conditions using the Unweighted Pair Group Average (UPGA) Pearson Correlation Iindex (Pielou, 1984; Ludwig & Reyholds, 1988).
Multivariate statistical analyses, performed by the computer program PC – ORD version 2.0 (ter Braak 1988, 1990), were used to identify relationship between the measured environmental variable and the species assemblages. Our calibration model included a total of 50 diatom taxa, using a cut-off criterion of >1% relative abundance. Because of space constraints and the limitations of inferring ecological preferences for rare taxa, we present here information for only the 40 most abundant diatom taxa (i.e. taxa with a relative abundance >2%).
Canonical Correspondence Analysis (CCA), using forward selection and Monte Carlo permutation tests, was then used to identify variables which were significant in explaining the variation in the diatom assemblages (ter Braak & Verdonschot 1995). Species data were square root transformed and rare taxa were down-weighted in order to maximize the signal:noise ratio within the data set.
Results
The nanoplankton from 21 sampling stations comprising of 134 taxa consisting predominantly of centric nanodiatom (29 species), pennate (40 species) and dinoflagellate (65 species) was collected from the Vietnam waters of the South China Sea (Appendix). Among the minute plankton collected were three species of centric nanodiatom (Minidiscus comicus, M. chilensis, M. trioculatus) and numerous other pennate species (Tables 1.1, 1.2 & 1.3).
The nanodiatom population in the Vietnam waters of the South China Sea toward the south was sparse (1.3 x 103 to 2.4 x 103 L-1) while the Vietnam waters toward the central and south wastern parts were high (5.7 x 103 to 3.9 x 103 L-1) (Fig. 2a). The dominant centric nanodiatom, ranging from 2.4 x 103 to 4.6 x 103 L-1 comprised of species of Thalassiosira, Minidiscus, Chaetoceros, Cyclotella and Stephanodiscus; while the dominant pennate nanodiatom (ranging from 8.9 x 103 to 16.7 x 103L1) comprised of species of Asterionella, Psammodiscus, Amphipleura, Navicula, Deadesmis, Fragilaria and Nitzschia (Fig. 2b).
The Diversity H and Evenness J indices were especially high in central Vietnam waters with values ranging from 1.5 – 3.1 and 0.70 to 0.87 respectively (Fig. 2c & d). The Thalassiosira species were dominant (ranging from 6.3 x 103 to 10.8 x 103 L-1) in the northern, central and southern Vietnamese waters; while the Minidiscus species (ranging from 5.8 x 103 – 8.14 x 103 L-1) were predominant to the north of central Vietnam waters (Fig. 2.1).
The Chaetoceros and Cyclotella species were less abundant ranging from 1.12 x 103 to 7.2 x
103 L-1 toward the southern and south eastern portion of the Vietnamese waters. The pennate species of Asterionella and Psammodiscus were also present in the south of the central Vietnamese waters with values ranging from 4.8 x 103 to 7.19 x 103 L-1) (Fig. 2.2). Patches of pennate species belonging to genera Amphipleura, Navicula, Diadesmis and Fragilaria with values ranging from 1.57 x 103 to 4.76 x 103 L-1 were also present (Fig. 2.3). The distribution of the pennate nanodiatom genera of Nitzschia (north and south west tips of the Vietnamese waters), Thalassionema (central and around Mekong Delta of the Vietnamese waters) and Fallacia (south west tip of the Vietnamese waters) had moderate values ranging from 1.02 x 103 to 2.84 x 103 L-1 (Fig. 2.4). The toxic dinoflagellate species of Pseudo nitzschia was less predominant (1.02 x 103 to 1.42 x 103 L-1) in the south of central Vietnamese waters.
Distribution of the nanodinoflagellate genera of Amphidoma and Centrodinium were widespread, stretching right from the central Vietnamese waters via the south to the south west of the Vietnamese waters with values ranging from 0.81 x 103 to 2.38 x 103 L-1 (Fig. 2.5). Species of Gonyaulax and Paleophalacroma were also present (0.8 x 102 to 9.5 x 102 L-1) in offshore Vietnam waters (Fig. 2.5c & d). The other 3 nanodinoflagellate species of Protoperidinium, Planodinium and Scrippsiella were present in lesser amounts (3.42 x 102 to 14.3 x 102 L-1) in the central and south western Vietnamese waters; while Prorocentrum species were found in considerable amounts (3.42 x 102 to 4.78 x 102 L-1) in the northern coastal and southwest offshore regions of the Vietnamese waters.
Species Distribution and Density in Vietnamese Waters
The three nanodiatom species of Minidiscus (M. comiscus, M chilensis, M. trioculus) were centric diatom whose density ranging from 4.08 x 103 to 7.34x 103 L-1; while the pennate forms consisted of the genera Navicula, Fragilaria, Diploneis, Pseudo-nitzschia and Amphiplaura including those belonging to the minute species whose size range was between 5-50µm (Tables 1.1 & 1.2). Some of the known Navicula species consisted of Navicula grevileana, N. schonkenii, N. fucicola and N.
pseudanglica var. signata (mean density 18.6 x 103 L-1); while the Thalassiosira species comprised of Thalassiosira tenera, T. climatosphaera, T. oestrupii var. ventrickae and T. pacifica (ranging 4.49 x 103 to 9.39 x 103 L-1). Among the nanodiatom, 5 genera were new records in the Vietnam waters during the study period.
Asterionella from nearshore had 4 species (2 of them are dominant) with a high total cell count (16749 L-1); while the toxic Pseudo-nitzschia species (total cell count of 2859 L-1) had 5 dominant species namely P. seriata, P. lineata, P. fraudulenta, P. tugula and Sabpacifica with values ranging from 4.08 x 102 to 12.2 x 102 L-1. The genera of Thalassiosira, Minidiscus, Chaetoceros, Stephanophyxis, Coscinodiscus and Navicula had numerous species (6 to 17 species) while the others (Amphipleura, Berkeleya, Raphoneis, Cosmioneis, Luticola, Cymbella) had only 1 to 2 species.
The mean nanodiatom cell density from nearshore stations was significantly (p<0.01) higher than those away from the coast (Figs. 3.1, 3.2 & 3.3, Table 2.1). The cell density of the nearshore, middle shore and offshore zones ranged from 9.3 x 103 to 30.2 x 103 L-1, 6.9 x 103 to 15.9 x 103 L-1 and 2.04 x 103 to 11.0 x 103 L-1 respectively. The pie chart diagram in percentage abundant of nanodiatom with depth shows that the percentage abundance is highest for the chlorophyll maximum layer (40.6%), followed by subsurface layer (32.6%), sub chlorophyll maximum layer (24%) and finally the thermocline layer (2.7%) (Fig. 3.4). The nanodiatom tend to aggregate at the chlorophyll maximum layer rather than at the other 3 levels namely subsurface, thermocline or sub chlorophyll maximum layer (Fig. 3.5, Table 2.2). The Thalassiosira and Minidiscus species were well distributed in the 4 depth zones while the other 4 dominant species of Fragilaria, Cocconeis, Pseudo-nitzschia and Navicula were found commonly in the chlorophyll maximum layer (Table 2.3).
Nanodinoflagellate Abundance
The dinoflagellate consisted of a wide range of species of Amphidoma, Centrodinium, Gonyaulax, Scrippsiella, Protoperidinium, Palaeophalacroma, Oxytoxum and Prorocentrum ; many of which were in the cyst forms found especially in the cental Vietnam waters (Table 3.1). The Vietnam waters of the South China Sea contained significantly (p>0.01) high cell density of Gonyaulax sp., Gymnodinium sp. and Amphidoma ; these species have the potential to form blooms. The presence of the dinoflagellate species of Protoperidinium sp. and Prorocentrum were detected in considerable amounts in the middle shore of Vietnam waters of the South China Sea. Related genera belonging to Haptophyceae comprising of Prymnesiaceae and Coccolithceae were rarely present in the Vietnam waters during the study period.
The nanodinoflagellate commonly found in the three zones of the Vietnam waters of the South China Sea comprised of 11 genera; among the genera, Amphidoma, Centrodinium and Gonyaulax were frequently sampled (Table 3.1). The offshore Vietnam waters had significantly (p<0.01) high nanodinoflagellate cell count when compared to those of the coastal or middle zones. The nanodinoflagellate distribution of the Vietnam waters showed that the highest cell density was at the subchlorophyll maximum layer; while the subsurface layer at the middle zone of the Vietnam waters had the highest cell count (Table 3.2). The nanodinoflagellate genera of Prorocentrum and Gonyaulax had a wide range of species (8 – 9 species) with cell density values ranging from 800 to 1225 L-1 especially at stations 55F and 52F (both offshore) respectively (Table 3.3). Prorocentrum comprised of 4 dominant species (P. gracile, P. micans, P. minimun and P. sigmoides) while Gonyaulax had also 4 main species (G. diagenis, G. polygramme, G. scrippsae, G. polyedro).
Species Association and Assemblage
The species assemblage in the Vietnam waters of the South China Sea consisted of at least 8 groups comprising of the combined pennate and centric nanodiatom (group A, B, D, E and F) as well as the groups consisting of the only centric nanodiatom member (group C, G and H) (Fig. 4.1, Table 4.1). The all centric nanodiatom member species assemblage comprised of group C (Mastogloia, Luticola, Cosmioneis), group G (Psammodiscus, Nitzschia, Raphoneis, Fragilaria, Amphipleura) and H (Navicula, Thalassionema).
The dendrogram from Fig. 4.2 shows the similarity in species community composition between stations in at least 5 groups (A, B, C, D and E) during the 1999 cruise survey in the Vietnam waters of the South China Sea. The 3 groups comprising of A, B and C were actually coastal zone stations while the other two were mixed stations (coastal and offshore). The species association or assemblage of nanodinoflagellate in the Vietnam waters comprises of 4 groups; namely group A (Gyrodinium, Centrodinium), group B (Palaeophalacroma, Amphidoma), group C (Scrippsiella, Gonyaulax) and group D (Planodinium, Goniodium) (Fig. 4.3, Table 4.2).
Canonical Correspondence Analysis
The environmental parameters for the water masses from different zone and depth layer are given in Table 5. The salinity and temperature profile values showed the existence of the thermocline stratified layer in the Vietnam waters of the South China Sea. The PC-ORD statistical program using the Canonical Correspondence Analysis (CCA) is used to show the relationship between the nanoplankton with the environmental physical factors of the water masses. The copper concentration in the Vietnam waters of the South China Sea (especially around the vicinity of the Mekong Delta) ranged from 3.2 to 9.7 nM in the water column (Hungspreugs et al., 1998).
The Canonical Correspondence Analysis (CCA) of algal species assemblage in the Vietnam waters during the April/June 1999 cruise showed that the majority of the species were dependent on
specific environmental parameters such as salinity, electrolyte metal concentration (especially Cu), depth and pH (Fig. 3.1, Table 5). The depth and salinity parameters were the strongest variable influencing algal assemblage composition within our sample set of species communities from different water masses.
High salinity and depth were characterized by a higher abundance of stenohaline species of Cymbella, Cosmioneis, Asterionella, Amphora, Psammodiscus and Mastogloia. Lower salinity values favoured species such as Nitzschia and Diploneis.
The pH value also showed significant (p>0.05) influence on certain species association and assemblage. Low pH values favoured association of species of Diadesmis, Pseudo-nitzschia and Fragilaria; while at higher pH favoured species of Thalassiosira and Minidiscus. The CCA analysis on the relationship between algal cells in the water masses from different water depth showed that the species such as Amphora, Psammodictyon and Berkeleya were sensitive to depth and salinity while Cyclotella and Navicula were sensitive to temperature. Thalassiosira and Minidiscus species were highly influenced by dissolved oxygen; whereas high pH value favoured the presence of Minidiscus.
The CCA analysis on the relationship between nanodinoflagellate in water masses from different depth showed that most species were dependent on two specific parameters namely, salinity and depth (Fig. 3.3). These two parameters were the strongest variable influencing nanodinoflagellate preference, especially species of Prorocentrum, Peridinium, Scrippsiella, Centrodinium and Goniodema. Other species of Gonyaulax, Amphidoma and Oxytoxum were dependent on temperature as environmental preference. Dissolved oxygen did not show any strong influence on the presence of dinoflagellate species; however, the influence of pH was even less.
Discussion
Prior to this present survey, a collaborative cruise in the waters of the South China Sea of the Western Philippines was conducted in the postmonsoon (April and May, 1998) periods on board MV SEAFDEC (Shamsudin & Kartini, 1999). Surprising, the most abundant nanoplanktonic Coccolithophorid species comprised of Emilinia huxleyi, Oolithotus fragilis and Gephyrocapsa oceanica (collectively up to 105 L-1) which occurred in sharp subsurface maximum chlorophyll layer down to 40 m depth; however, these species never occur in the Vietnam waters during the study period. The cosmopolitan Coccolithophorid species in the Philippines waters originated from the ocean gyre of the central Pacific ocean; whereas the Vietnam waters are completely block from this gyre by long streaches of islands (eg. Spratly island to the south east and Paracel island in the centre of Vietnam waters) including the Philippines.
The other explanation is probably due to the seasonality occurrence of the Coccolithophorid in the seawater (Hallegraeff, 1984). The 4 physical factors influencing the dynamic motion in the sea comprise of the pressure gradient, Coriolis force, gravity and friction. The calculated dynamic height of the sea surface can be obtained (usually <1m) when the slope of the sea surface in the ocean gyre circulation is formed due to the geostrophic surface current which has the tendency to balance the pressure gradient. The surface gyre sea water circulation plays an important role in transporting nanoplankton from a given region to the other in the ocean. The sea surface height anomaly from the Topex/Ers-2 analysis (satellite data) can also be used to explain this phemomenon (Snidvongs – personal communication).
The nanoplankton (including the smaller microplanktonic species) from 31 sampling stations during the 1998 cruise consisted of more than 200 taxa comprising predominantly of nanodiatom (>150 species), Dinoflagellata (>30 species) and Prasinophyta (>18 species). However, the present study in the Vietnam waters showed that the nanoplankton comprised of centric and pennate diatoms
as well as the nanodinoflagellate. The coccolithophorids in the Australian waters of the South China Sea showed a dominant change from Emiliania huxleyi to Gephyrocapsa oceanica and a southward transport of many tropical species (eg. Scyphosphaera apsteinii and S. pulichra (Hallegraeff, 1984).
Among the minute plankton collected during the 1998 cruise of the Philippines waters of the South China Sea, three species of the nanodiatom (Minidiscus comicus, M. chilensis, M. trioculatus) and numerous flagellate species were present. The dominant pennate diatom comprised of Synedra parasitica, Fragilaria brevistriate, Diploneis crabro and Neodenticula sp., all of which were <20 µm in size. However, the present study in the Vietnam waters shows high density of centric nanodiatom especially Thalassiosira and Minidiscus species. The central diatom comprised of Cyclotella striata, C. meneghiniana and Stephenopyxis palmeriana were also encountered.
In both study areas, the genera of Synedra, Navicula, Fragilaria and Thalassiosira contained a wide range of species; while those of dinoflagellate consisted of a wide range of species of genera Gyrodinium, Pyrodinium, Gonyaulax, Scrippsiella, Protoperidinium, Protoceratium, Ceratocorys and Alexandrium. The genera of Protoperidinium, Minidiscus and Thalassiossira had a wide range of species. The total nanoplankton population in the Philippines waters was dense in nearshore regions (especially around Subic and Manila bays) and tend to spread out in concentric semicircle into the open sea. The presence of the dinoflagellate species of Protoperidinium and Alexandrium were detected in considerable amounts at nearshore and midshore Philippines waters of the South China Sea. However, high density of the nanodinoflagellate species of Amphidoma and Centrodinium were present in the Vietnam waters.
Semina and Tarkhova (1972) recorded 1000 species of phytoplankton, mainly of diatoms and dinoflagellates in the Pacific Ocean. They also reported that the only other conspicuous marine microplanktonic forms are the spherical green cells belonging to Prasinophyta (Halosphaera, Pterosperma) and the bundles of filaments of the Cyanophyte genus, Trichodesmium (Oscillatoria):
both of these groups tend to float to the surface, the former buoyed up by oil globules and the latter by gas vacuoles in the cells. The nanoplankton is almost entirely composed of small flagellate cells belonging to the Prymnesiophyta. They possess two flagella with a haptonema. This group now contains the genera of the Prymnesiales (= Coccolithophoridaceae) since many of these have been shown to possess a haptonema. Some are delicate and are assually damage beyond recognition or are destroyed by preservatives (formalin, is not an ideal preservative for phytoplankton) and their numerical abundance is rarely determined.
Prymnesiophyta bearing calcareous plates (coccoliths) are more easily damage than the delicate forms bearing organic scales (Chrysochromulina), but the latter can make up a considerable amount of the biomass in some seas. It is also interesting to note that the present study did not show that Prasinophyta and Phrymnesiophyta were present in the Vietnam waters of the South China Sea. An increase in the diversity value of the nanoplankton population could be due to an increased number of species or even distribution of individuals per species as described by Gray (1981). In reality, such community organisation is constantly acted on by biological and physical factors in many different ways to produce, perhaps a different organisation in the future as a response to such environmental changes.
When a bloom occurs, only a few plankton species will predominate and thus effect or influence the number of species or the even distribution of individual species.
Nanoplankton species tend to occur in groups throughout natural communities and it ought to be possible to distinguish associations of species in the plankton. Observations from some detailed surveys and from the continuous plankton recorded certainly suggest that there are discrete associations.
These associations appear to be linked with geographical zones (currents, water masses) rather than with subtle differences in water chemistry. The present cruise survey shows that the bulk of the nanoplankton comprised of nanodiatom, dinoflagellate and flagellate; all of these organisms reach a
value close to 150 taxa, many of which are yet to be carefully identified.
The fact that the nanoplankton is small should not lead to its neglect since in many waters it is responsible for more carbon fixation than the more immediately obvious microplankton. On an annual basis 70-80%(total carbon 82-78 meq m-2) was attributable to the nanoplankton. McCarthy, Rowland Taylor & Loftus (1974) found that over a two year study in Chesapeake Bay the nanoplankton (in this case species passing through a 35 mm mesh net) was responsible for 89.6% of the carbon fixation.
In the open ocean, especially in oligotrophic regions, the nanoplankton are often the most abundant organisms (Hulbert, Ryther & Guillard, 1960). Pomeroy (1974) gives a table which shows that over 90% of total fixation is by forms smaller than 60 µm in diameter. It is necessary to measure cells and to calculate cell volumes if more detailed information of the biomass of individual species species is required. The nanoplankton together with the Coccolithophoridaceae were present in significant quantities and many of these organisms are minute having the size range between 5 to 50 µm; these organisms have been shown to contribute >50% in total biomass and productivity in the sea.
Acknowledgements
The authors would like to thank the Captain and the crews of the MV SEAFDEC for collecting water samples during the cruise; Che Ku Haslinda (Kolej Universiti Terengganu, Malaysia) for her help in mapping out the microplankton population and for typing this manuscript.
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Fig. 2. a) Total cell/L density, b) Dominant nanoplankton species, c) Diversity H index and d) Evenness J index in the Vietnamese waters of the South China Sea (April-June 1999 cruise survey).
10 4 10 6 10 8 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
13 5 0 24 5 0 35 5 0 46 5 0 57 5 0 68 5 0 79 5 0
a) Total cell/L
Longitude
Latitude
Longitude
Latitude
104 106 108 110 112 114
6 8 10 12 14 16 18 20 22
104 106 108 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
Asterionella Psammodiscus Chaetoceros Fragilaria Thalassiosira Minidiscus
Diadesmis Raphoneis Thalassionema b) Dominant species/L
1 0 2 1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
0 .0 85 0 .5 85 1 .0 85 1 .5 85 2 .0 85 2 .5 85 3 .0 85
c) H
Longitude
Latitude
1 04 1 06 1 08 1 10 1 12 1 14
6 8 10 12 14 16 18 20 22
0.1 650 0.3 000 0.4 350 0.5 700 0.7 050 0.8 400 0.9 750
d) J
Longitude
Latitude
Fig. 2.1. Distribution of the centric nanodiatom genera (a) Thalassiosira, (b) Minidiscus, (c) Chaetocerosand (d) Cyclotella in the Vietnamese waters of the South China Sea (April-June 1999 cruise survey).
1 02 1 04 1 06 1 08 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
18 2 0 33 2 0 48 2 0 63 2 0 78 2 0 93 2 0 1 08 20
a) Thalassiosira sp./L
Longitude
Latitude
1 0 2 1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 3 60 2 4 90 3 6 20 4 7 50 5 8 80 7 0 10 8 1 40
b) Minidiscus sp./L
Longitude
Latitude
10 4 1 0 6 10 8 1 1 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
12 0 0 22 0 0 32 0 0 42 0 0 52 0 0 62 0 0 72 0 0
10 4 10 6 10 8 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
c) Chaetoceros sp./L
Longitude
Latitude
104 1 06 1 08 1 10 1 12 114
6 8 10 12 14 16 18 20 22
200 430 660 890 11 20 13 50 15 80
d) Cyclotella sp./L
Longitude
Latitude
1 04 1 06 1 08 110 112 114
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
Fig. 2.2. Distribution of the centric nanodiatom genera (a) Stephanodiscus, (b) Stephanophyxis ; the pennate genera (c) Asterionella and (d) Psammodiscus in the Vietnamese waters of the South China Sea (April-June 1999 cruise survey).
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
2 50 5 40 8 30 11 2 0 14 1 0 17 0 0 19 9 0
Longitude
Latitude
a) Stephanodiscus sp./L
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
10 4 10 6 10 8 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
15 0 37 5 60 0 82 5 10 5 0 12 7 5 15 0 0
b) Stephanophyxis sp./L
Longitude
Latitude
10 4 10 6 10 8 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
8 00 1 86 5 2 93 0 3 99 5 5 06 0 6 12 5 7 19 0
Longitude
c) Asterionella sp./L
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
Latitude 10 4 1 0 6 1 08 1 1 0 1 12 11 4
6 8 10 12 14 16 18 20 22
80 0 1 8 0 0 2 8 0 0 3 8 0 0 4 8 0 0 5 8 0 0 6 8 0 0
d) Psammodiscus sp./L
Longitude
Latitude
1 04 1 06 1 08 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
Fig. 2.3. Distribution of the pennate nanodiatom genera (a) Amphipleura, (b) Navicula, (c) Diadesmis and (d) Fragilaria in the Vietnamese waters of the South China Sea ( April-June 1999 cruise survey).
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
4 5 0 8 7 5 1 3 0 0 1 7 2 5 2 1 5 0 2 5 7 5 3 0 0 0
a) Amphipleura sp./L
Longitude
Latitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 02 10 4 10 6 1 08 11 0 1 12 11 4
6 8 10 12 14 16 18 20 22
68 0 1 36 0 2 04 0 2 72 0 3 40 0 4 08 0 4 76 0
1 04 1 06 1 08 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
b) Navicula sp./L
Longitude
Latitude
10 4 1 0 6 1 08 1 1 0 1 12 11 4
6 8 10 12 14 16 18 20 22
47 0 86 5 12 60 16 55 20 50 24 45 28 40
1 04 1 06 1 08 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
Latitude
Longitude
c) Diadesmis sp./L
104 1 0 6 108 1 1 0 11 2 114
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
31 5 63 0 94 5 12 6 0 15 7 5 18 9 0 31 5 0
d) Fragilaria sp./L
Longitude
Latitude
Fig. 2.4. Distribution of the pennate nanodiatom genera (a) Nitzschia, (b) Thalassionema, (c) Fallacia and (d) Pseudo-nitzschia in the Vietnam waters of the South China Sea (April /June 1999 cruise survey).
10 2 10 4 10 6 10 8 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
47 0 86 5 12 6 0 16 5 5 20 5 0 24 4 5 28 4 0
a) Nitzschia sp./L
Longitude
Latitude
10 4 10 6 10 8 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
34 0 68 0 1 02 0 1 36 0 1 70 0 2 04 0 2 38 0
10 4 10 6 10 8 11 0 11 2 11 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
b) Thalassionema sp./L
Longitude
Latitude
10 4 10 6 10 8 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
47 0 86 5 12 6 0 16 5 5 20 5 0 24 4 5 28 4 0
c) Fallacia sp./L
Longitude
Latitude
10 4 10 6 10 8 11 0 11 2 11 4
6 8 10 12 14 16 18 20 22
1 02 1 04 1 06 1 08 110 112 114
6 8 10 12 14 16 18 20 22
204 408 612 816 1 02 0 1 22 4 1 42 8
d) Pseudo-nitzschia sp./L
Longitude
Latitude
Fig. 2.5. Distribution of the nanodinoflagellate genera (a) Amphidoma, (b) Centrodinium, (c) Gonyaulax and (d) Palaeophalacroma in the Vietnamese waters of the South China Sea (April- June 1999 cruise survey).
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
34 0 68 0 10 2 0 13 6 0 17 0 0 20 4 0 23 8 0
a) Amphidoma sp./L
Longitude
Latitude
1 04 1 06 1 08 1 10 1 12 1 14
6 8 10 12 14 16 18 20 22
1 4 0 2 7 5 4 1 0 5 4 5 6 8 0 8 1 5 9 5 0
b) Centrodinium sp./L
Longitude
Latitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 4 0 2 7 5 4 1 0 5 4 5 6 8 0 8 1 5 9 5 0
c) Gonyaulax sp./L
Longitude
Latitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 40 2 75 4 10 5 45 6 80 8 15 9 50
d) Palaeophalacroma sp./L
Longitude
Latitude
Fig. 2.6. Distribution of the nanodinoflagellate genera (a) Protoperidinium, (b) Planodinium, (c) Prorocentrum and (d) Scrippsiella in the Vietnamese waters of the South China Sea (April - June 1999 cruise survey).
1 0 4 1 0 6 1 08 1 1 0 1 12 1 1 4
6 8 10 12 14 16 18 20 22
1 4 0 2 7 5 4 1 0 5 4 5 6 8 0 8 1 5 9 5 0
a) Protoperidinium sp./L
Longitude
Latitude
1 04 1 06 1 08 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 04 1 06 1 08 1 10 1 12 1 14
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
2 00 4 05 6 10 8 15 1 02 0 1 22 5 1 43 0
b) Planodinium sp./L
Longitude
Longitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
7 0 1 3 8 2 0 6 2 7 4 3 4 2 4 1 0 4 7 8
c) Prorocentrum sp./L
Longitude
Latitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
1 4 0 2 7 5 4 1 0 5 4 5 6 8 0 8 1 5 9 5 0
Latitude
d) Scrippsiella sp./L
Longitude
1 0 4 1 0 6 1 0 8 1 1 0 1 1 2 1 1 4
6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2
0 5000 10000 15000 20000 25000 30000 35000
Nearshore Middleshore Offshore
14
20 29
38 57
58
5 9
15 19 22
27 50
11 16 17 24
42 52 55
Fig. 3.1. Distribution and abundance of nanodiatom from chlorophyll maximum layer at 3 different zones in the Vietnamese waters (cruise April-June 1999).
Fig. 3.2. Nanodiatom abundance (L-1) of selected stations from different zones (coastal, middle and offshore) during the April-June 1999 cruise in the Vietnam waters (S – subsurface, T - thermocline, CM – chlorophylla maximum, B – sub chlorophyll maximum layer).
Fig. 3.3. Distribution and abundance of nanodiatom species (centric, pennate) in the Vietnamese waters (cruise April-June 1999).
0 500 1000 1500 2000 2500
Species
Mean cell/L
Centric Pennate
Thalassiosira sp.
Nitzschia sp.1 0
5,000 10,000 15,000 20,000 25,000
S T CM B
cell/L
N M O
Fig. 3.5. Distribution and abundance of nanodiatom from different depth level (S – sub surface, T – thermocline, CM – chlorophyll maximum layer, B – sub chlorophyll maximum layer) from selected stations (1, 24, 27) in the Vietnamese waters (cruise April-June 1999).
Fig. 3.6. Distribution and abundance of nanodiatom cell from different depth (S – sub surface, T – thermocline, CM – chlorophyll maximum layer, B – sub chlorophyll maximum layer) from selected stations (1, 24, 27) in the Vietnamese waters (cruise April-June 1999).
Fig. 3.4. Pie-chart graph in percentage abundance of nanodiatom with depth from selected stations during the April-June 1999 cruise in the Vietnamese waters (S – subsurface, T – thermocline, CM – chlorophylla maximum, B – sub chlorophyll maximum layer).
0 5000 10000 15000 20000 25000
S T CM B
Nos/L
Nearshore (1) Middleshore (27) Offshore (24)
0 5000 10000 15000 20000 25000 30000 35000 40000 45000
Mean cell/L
S T CM B
32.56%
S 24.03%
B
2.71%
T 40.70%
CM
S T CM B
Tree Diagram for 12 Cases Unweighted pair-group average
1-Pearson r
Linkage Distance 0 . 2 0 . 4 0 . 6 0 . 8 1 . 0 1 . 2 1 . 4
Unknown Sp. 5 Unknown Sp.6 Centrodinium sp. Unknown Sp. 2 Unknown Sp. 1 Planodinium sp. Peridinium sp. Scrippsiella sp. Gonyaulax sp. Prorocentrum sp. Palaeophalacroma s Amphidoma sp.
Linkage Distance
0.0 0.2 0.4 0.6 0.8 1.0 1.2
17.Amphora 34.Navicula sp.2 32.Thalassionema 28.Navicula sp.1 30.Nitzschia sp.1 24.Raphoneis 22.Psammodiscus 19.Fragilaria 15.Amphipluera 20.Cyclotella 16.Cymbela 29.Fragilaria sp.1 31.Fallacia 12.Psammodictyom 10.Chaeto 9. Nitzschia 23.Diadesmis 7. Diploneis 26.Stephanodiscus 6. Navicula 25.Nitzschia sp.2 33.Berkeleya 18.Coscinodiscus 14.Cosmioneis 27.Luticola 8. Mastogloia 21.Astrionella 5. Pseudo-nitzschia 4. Cocconeis 13.Stephanophyxis 11.Cylindrotheca 3. Fragilaria 2. Minidiscus 1. Thalassiosira B A
C
D F E
G H
Fig. 4.1. Dendrogram showing nanodiatom species association during the 1999 cruise survey in the Vietnamese waters (cruise April-June 1999).
Fig. 4.2. Dendrogram showing similarity between stations in the Vietnamese waters (cruise April - June1999).
Fig. 4.3. Dendrogram showing nanodinoflagellate species association in Vietnamese waters (cruise April - June 1999).
Linkage Distance
0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
STN_50 STN_57 STN_42 STN_52 STN_27 STN_29 STN_19 STN_15 STN_55 STN_58 STN_16 STN_24 STN_38 STN_17 STN_20 STN_11 STN_14 STN_9 STN_5 STN_22 STN_1
B A C
D E