Научная статья на тему 'Meiobenthos communities for different mangrove types in Can Gio Biosphere Reserve, Vietnam'

Meiobenthos communities for different mangrove types in Can Gio Biosphere Reserve, Vietnam Текст научной статьи по специальности «Биологические науки»

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Ключевые слова
CAN GIO MANGROVE / MEIOFAUNA / NEMATODES / SEASONAL / МАНГРОВЫЕ ЛЕСА КАН ГИО / МЕЙОФАУНА / НЕМАТОДЫ / СЕЗОННЫЙ

Аннотация научной статьи по биологическим наукам, автор научной работы — Dinh Tu Nguyen, Thi Man Pham, Thi Xuan Phuong Nguyen, Phu Hoang Lai, Ann Chen - Cheng

Мангровые леса Кан Зъо это первый биосферный заповедник Вьетнама, созданный с 2000 г., общей площадью 75740 га. Основные населяющие его виды это восстановленные мангровые деревья (23028 га, из которых 96,7 % занимают Rhizophora apiculata) и естественно возобновлённые мангровые деревья, 7829 га). Мейобентосные сообщества исследовались в зал. Ракх Ок. Образцы были взяты на илистой отмели и из трёх различных видов мангровых деревьев от устья до верхних плёсов залива: из натуральных лесов авиценнии (Avicennia); натуральных смешанных лесов авиценнии и ризофоры (Rhizophora) и восстановленных лесов ризофоры в течение как сухого сезона, так и в период сезона дождей. Мейобентосная структура в основном включает в себя нематоды, копеподы, науплии, фораминиферы, полихеты (многощетинковые черви), олигохеты (малощетинковые черви), киноринхи, клещи (Acarus), остракоды (раковинчатые) и другие менее распространенные группы (двустворчатые моллюски, гастроподы, личинки насекомых, турбеллярии, разноногие ракообразные, немертины). Плотность мейобентоса в смешанных лесах была выше, чем в лесах авиценнии и ризофоры. Плотность мейобентоса в сухой сезон была выше, чем в сезон дождей. Плотность нематод и копепод возрастала, в то же время количество науплии и фораминифер сокращалось в сухой сезон.

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Can Gio mangrove is the first Biosphere Reserve of Vietnam created since 2000, with a total area of 75,740 ha. The major habitat types are rehabilitated mangrove (23,028 ha, in there Rhizophora apiculata with 96.7 %), and naturally regenerating mangrove (7,829 ha). Meiobenthic communities were investigated along Rachoc Creek. The samples were taken within a mud flat (Mud) site and 3 different types of mangrove from mouth to upper reaches of the creek: natural Avicennia (Avi) forest; natural mixed forest of Avicennia and Rhizophora (Mix) and rehabilitated Rhizophora (Rhi) forest during both dry and rainy seasons in. Meiobenthic composition mainly included nematodes, copepods, nauplii, foraminifera, polychaetes, oligochaetes, kinorhynchs, acari, ostracods, and others less abundant group (bivalves, gastropods, insect lavae, turbelaria, amphipods, nemertinea). Meiobenthic densities in Mixed forest were higher than in Avicennia forest or Rhizophora forest. Nematodes were most abundant in all stations and percentages in Mixed forest and Mudflat site were higher than in Avicennia and Rhizophora forests. Meiobenthic density in dry season was higher than in rainy season. Nematode and copepod densities increased, in the meantime nauplius and foraminifera reduced in dry season.

Текст научной работы на тему «Meiobenthos communities for different mangrove types in Can Gio Biosphere Reserve, Vietnam»

УДК 591.524.12

Dinh Tu Nguyen1*, Thi Man Pham1, Thi Xuan Phuong Nguyen1, Phu Hoang Lai1, Ann Chen - Cheng2 and Vu Thanh Nguyen1

institute of Ecology and Biological Resources (IEBR) Vietnam Academy of Science and Technology (VAST) 2Borneo Marine Research Institute, Universiti Malaysia Sabah, Malaysia

MEIOBENTHOS COMMUNITIES FOR DIFFERENT MANGROVE TYPES IN CAN GIO BIOSPHERE RESERVE, VIETNAM

Can Gio mangrove is the first Biosphere Reserve of Vietnam created since 2000, with a total area of 75,740 ha. The major habitat types are rehabilitated mangrove (23,028 ha, in there Rhizophora apiculata with 96.7 %), and naturally regenerating mangrove (7,829 ha). Meiobenthic communities were investigated along Rachoc Creek. The samples were taken within a mud flat (Mud) site and 3 different types of mangrove from mouth to upper reaches of the creek: natural Avicennia (Avi) forest; natural mixed forest of Avicennia and Rhizophora (Mix) and rehabilitated Rhizophora (Rhi) forest during both dry and rainy seasons in. Meiobenthic composition mainly included nematodes, copepods, nauplii, foraminifera, polychaetes, oli-gochaetes, kinorhynchs, acari, ostracods, and others less abundant group (bivalves, gastropods, insect lavae, turbelaria, amphipods, nemertinea). Meiobenthic densities in Mixed forest were higher than in Avicennia forest or Rhizophora forest. Nematodes were most abundant in all stations and percentages in Mixed forest and Mudflat site were higher than in Avicennia and Rhizophora forests. Meiobenthic density in dry season was higher than in rainy season. Nematode and copepod densities increased, in the meantime nauplius and foraminifera reduced in dry season.

Key words: Can Gio mangrove, meiofauna, nematodes, seasonal.

Динь Ту Нгуен1 , Тхи Ман Фам1, Тхи Суан Фуонг Нгуен1, Фу Хоанг Лай 1, Анн Тен - Тенг2 и By Тхань Нгуен 1 МЕЙОБЕНТОСНЫЕ СООБЩЕСТВА В МАНГРОВЫХ ЛЕСАХ РАЗЛИЧНОГО ТИПА В БИОСФЕРНОМ ЗАПОВЕДНИКЕ КАН ЗЬО, ВЬЕТНАМ

Мангровые леса Кан Зъо - это первый биосферный заповедник Вьетнама, созданный с 2000 г., общей площадью 75740 га. Основные населяющие его виды - это восстановленные мангровые деревья (23028 га, из которых 96,7 % занимают Rhizophora apiculata) и естественно возобновлённые мангровые деревья, 7829 га). Мейобентосные сообщества исследовались в зал. Ракх Ок. Образцы были взяты на илистой отмели и из трёх различных видов мангровых деревьев от устья до верхних плёсов залива: из натуральных лесов авиценнии (Avicennia); натуральных смешанных лесов авиценнии и ризофоры (Rhizophora) и восстановленных лесов ризофоры в течение как сухого сезона, так и в период сезона дождей. Мейобентосная структура в основном включает в себя нематоды, копеподы, науплии, фораминиферы, полихеты (многощетинковые черви), олигохеты (малощетинковые черви), киноринхи, клещи (Acarus), остракоды (раковинчатые) и другие менее распространенные группы (двустворчатые моллюски, гастроподы, личинки насекомых, турбеллярии, разноногие ракообразные, немертины). Плотность мейобентоса в смешанных лесах была выше, чем в лесах авиценнии и ризофоры. Плотность мейобентоса в сухой сезон была выше, чем в сезон дождей. Плотность нематод и копепод возрастала, в то же время количество науплии и фораминифер сокращалось в сухой сезон.

Ключевые слова: мангровые леса Кан Гио, мейофауна, нематоды, сезонный.

I. Introduction

Mangroves provide physical protection for communities in low lying coastal areas, more importantly, they are believed to play a major role in supporting tropical estuarine and coastal food web (Alongi & Christoffersen, 1992), by providing a major source of organic material and acting as nursery grounds and habitats for commercially important brackish water fish species (Robertson & Duke, 1987, Pinto & Punchihewa, 1996). Effort to rehabilitate Can Gio mangrove started since 1978. Rhizophora apiculata was chosen as they were fast growing tree and would be able to restore

forest cover at the fastest rate, otherwise the tree with the highest commercial value. Since 1984, other tree species, such as Intsia bijuga, Ceriops tagal, C. decandra, Lumnitzera racemosa, Xylo-carpus granatum, Thespesia populnea were planted on higher land to recover the barren land at higher altitudes (Le Duc Tuan et al., 2002).

Meiobenthos are mobile, sometimes also hapto-sessile animals, smaller than macrobenthos, but large than microbenthos. The size boundaries of meiobenthos are based on the standardized mesh width of sieve 500 pm (1000 pm) as upper and 42 pm (or 63 pm) as lower limit: all fauna passing the coarse sieve, but retained by the fine sieve is considering meiobenthos (Giere, 1993). In 2000, Olafsson et al. published a research of influences of spring tide inundation on meiobenthos of hypersaline tropical mangrove sediment. Recently, the first study on ecology of meiofauna in mangrove of the Red Sea was presented by Khalil (2001). In Vietnam there are only few studies concerning meiobenthos including nematodes in the mangroves. These initial studies were only concentrated on identification of free-living nematodes without taking into consideration of meiobenthic community structure as well as forest structure (rehabilitated vs natural forest) and its age (Nguyen Vu Thanh & Doan Canh, 2000; Gagarin & Nguyen Van Thanh, 2004; Nguyen Vu Thanh & Gagarin, 2004; Nguyen Thi Thu et al., 2004, Nguyen Vu Thanh et al., 2005, Lai Phu Hoang et al, 2005 and Gagarin & Nguyen Vu Thanh, 2006).

II. Materials and methods

II. 1. Study area and location: The study was carried out in Can Gio Mangrove Biosphere Reserve, located about 65 km in the south of Ho Chi Minh City with latitude: 10 °22'14''-10 °40'09'' and longitude: 106 °46'12''-107 °00'59''.

II. 2. Sampling and data collection

Sampling times and sites/stations:Meiobenthic communities were investigated in Rachoc (RO) creek in Can Gio Forestry Park area. These creeks flow in nearly right angle direction to Dong

Tranh River. Along the creek from the mouth to upper reaches, there are representatives of natural and rehabilitated mangrove forests. On the bank of Dong Tranh River and mouth of the creek there are natural forest with abundance of Avicennia alba, in the upper reaches there are rehabilitated forests with single species Rhizophora apiculata (since 1978-1982). In between two forest types there are mixed forests. These are also natural regeneration forest, including two main species Avicennia alba, Rhizophora apiculata, and others such as Excoecaria agallocha, Xylocarpus spp, Aegyceras spp, Lumnitzera spp (fig. 1).

Four sites were selected in range of mangrove forests including mud flat site (Mud) and three types of mangroves: natural Avicennia forest (Avi), natural mixed forest (Mix), rehabilitated Rhizophora forest (Rhi). The samples were collected in both creek banks "a" and "b" at three intertidal stations: low water tide (1), middle water tide (2), high water tide (3); and a station at shallow water subtidal zone "c". In the mud flat (Mud) of a creek, four stations were sampled. (fig. 1).

Fig. 1. Map of mangrove zones and sampling sites/stations in Can Gio Mangrove Biosphere Reserve, Ho Chi Minh City of Vietnam

Sampling, extraction and preparation of permanent slides: Samples were taken by a hand corer of 40 cm length and inner diameter of 10 cm2 (0 = 3,5 cm). Sediment was collected to a depth of 10 cm at each sampling station These were preserved in 5 % neutralized formalin heated up to the point of 60-70 °C. Some hydrological parameters of the water were measured such as temperature (T), pH, salinity (NaCl), electric conductivity (EC), dissolved oxygen (DO), turbidity (Tu) at the time of the sampling procedure by the TOA (Model WQC-22A).

Decantation and Ludox extraction: The sediments were sieved through 1mm mesh size (to separate the coarse shells and plant remains from the sediment). The samples then were rinsed with tap water in a 5 litre beaker. After settlement (10 seconds) the supernatant was poured through a 63 pm. The rinsing and decantation were repeated 10 times until the water became clear. After decantation, the sample consisting of a small amount of material was carefully washed bringing the extracted portion of the sediment to one side of the sieve. Then it was washed into a large beaker using Ludox (Heip et al, 1985). At least 3 times the sample volume of Ludox solution was added, and stirred. Then it was left to settle for at least 40 minutes. Finally, the supernatant was carefully poured through a 40pm sieve. This process was repeated 3 times. The extracted fauna was washed thoroughly with tap water and then preserved with FAA (Formalin Acid Acetic) solution in a suitable container.

Data analysis: The extracted meiobenthos were categorized into the different higher taxonomic groups (nematodes, polychaete, copepods,...) under a stereomicroscope based on works of Higgins & Thiel (1988) and Giere (1993). Univariate measures were statistically tested using SPSS 13.0 software package. Differences of meiobenthic densities and biodiversity indexes between sites/stations were tested using one-way analysis of variance (ANOVA), based on lg(x+1) transformed data.

III. Results

III.1. Abiotic factors

Temperatures changed not much from 28 °C to 30,7 °C at different stations and seasons. Dissolved oxygen index (DO) varied among stations and seasons. DO trended to reduce from Rhizo-phora site to Avicennia site. pH index was nearly similar at three study stations. In the dry season, pH was a little higher than in the rainy season. The result of salinity showed that salinity increased from Avicennia site to Rhizophora site. Comparison of salinity between 2 seasons, result showed that salinity increased quite much from the rainy season to the dry season. In the rainy and dry seasons, turbidity index (Tu) also increased from Avicennia site to Rhizophora site. In contract, turbidity index decreased from Avicennia site to Rhizophora site in the rainy season.

III. 2. Changes in meiobenthic abundance

III. 2. 1. Total meiobenthos

In the dry season, average meiobenthic density was 2803 ind/10 cm2, increased drastically approximately 30 % in comparison with density in the rainy season. Increased density was main in Mixed and Mudflat sites with 3129 and 3420 ind/10 cm2 (average density increased 43-48%) (tabl. 1). Density of meiobenthos in Mudflat site was significantly higher than in Rhizophora and Avicennia sites. On the other hand, meiobenthic density in Mixed site was higher than in Rhizophora and Avicennia sites, but not significantly different among Rhizophora, Mixed and Avicennia sites (P>0,05) (fig. 2,A). Among Mudflat stations, meiobenthic density in station Mud-4 was higher significantly than in Mud-2 and Mud-3 (P<0,05).

Table 1

Meiobenthic composition in Rachoc Creek in the dry season 2013

Order Station Meiobenthic composition

Ne Co Na Po Ol Ki Ac Os Fo Ot Sum

1 RO-Mud-1 3455 68 27 7 13 0 2 2 7 28 3608

2 RO-Mud-2 1823 35 20 8 5 0 2 10 10 55 1968

3 RO-Mud-3 2717 140 30 13 5 2 0 0 7 71 2985

4 RO-Mud-4 4908 113 27 3 5 3 0 7 0 50 5117

Ave Mud 3226 89 26 8 7 1 1 5 6 6 3420

Percentage 94,3 2,6 0,8 0,2 0,2 0 0 0,1 0,2 0,2 100

5 RO-Avi-al 2867 70 27 7 3 7 10 3 18 57 3068

6 RO-Avi-a2 1145 70 22 0 3 3 5 13 22 47 1330

7 RO-Avi-a3 1175 103 35 8 5 13 2 3 15 65 1425

8 RO-Avi-bl 5093 85 57 7 7 10 8 5 20 55 5347

9 RO-Avi-b2 2657 102 53 8 2 12 8 10 13 76 2941

10 RO-Avi-b3 1837 153 38 3 0 15 3 12 25 56 2143

11 RO-Avi-c 412 15 3 2 0 0 5 0 13 39 489

Ave Avi 2169 85 34 5 3 9 6 7 18 57 2392

Percentage 90,7 3,6 1,4 0,2 0,1 0,4 0,2 0,3 0,8 2,4 100

12 RO-Mix-al 3682 137 57 3 7 0 23 2 22 50 3982

13 RO-Mix-a2 3313 65 17 5 0 5 2 0 20 74 3500

14 RO-Mix-a3 2958 20 28 2 7 0 0 0 75 61 3151

15 RO-Mix-bl 2950 85 15 2 8 5 2 2 43 56 3168

16 RO-Mix-b2 3188 115 32 7 3 10 7 0 40 63 3465

17 RO-Mix-b3 2992 143 80 7 2 2 2 3 35 55 3320

18 RO-Mix-c 1198 48 28 0 2 0 3 0 7 33 1319

Ave Mix 2897 88 37 4 4 3 5 1 35 56 3129

Percentage 92,6 2,8 1,2 0,1 0,1 0,1 0,2 0 1,1 1,8 100

19 RO-Rhi-al 2873 160 75 0 10 2 18 2 78 40 3258

20 RO-Rhi-a2 1110 132 52 0 0 0 10 0 222 33 1558

21 RO-Rhi-a3 1213 117 52 0 2 2 5 0 208 18 1616

22 RO-Rhi-bl 2972 115 28 2 7 0 8 15 40 58 3244

23 RO-Rhi-b2 1653 78 42 2 7 0 10 0 238 53 2083

24 RO-Rhi-b3 1532 113 62 0 7 0 8 2 283 16 2022

25 RO-Rhi-c 3745 57 30 3 10 2 8 0 32 68 3954

Ave Rhi 2157 110 49 1 6 1 10 3 157 41 2534

Percentage 85,1 4,4 1,9 0 0,2 0 0.4 0,1 6,2 1,6 100

Average 2539 94 37 4 5 4 6 4 60 51 2803

Percentage 90,6 3,3 1,3 0,1 0,2 0,1 0,2 0,1 2,1 1,8 100

Ne: Nematodes Co: Copepods Na: Nauplii Po: Polychaetes Ol: Oligochaetes Ki: Kinorhynchs Ac: Acari Os: Ostracods Fo: Foraminifera Ot: Others

Density in Mud-1 was significantly higher than in Mud-2 (P<0,05), but not significantly different than in stations Mud-4 and Mud-3 (P>0,05) (fig. 3, A). In Avicennia site, density in Avi-a1 was significant higher than Avi-a3 (P<0,05). In addition, density in station Avi-b1 also was significant

higher than station Avi-b2 and Avi-b3 (P<0,05). In subtidal station Avi-c, density was significantly lower than all other stations (P<0,05) (fig. 3, B). Between stations in Mixed site, there was no significant difference between intertidal stations, but subtidal station Mix-c was also significant lower than other intertidal stations (P<0,05) (fig. 3, C). In Rhizophora site, density of meiobenthos in station Rhi-a1 significant higher than station Rhi-a2 and Rhi-a3 (P<0,05), station Rhi-b1 was generally higher than stations Rhi-b2 and Rhi-b3 but no significant difference (P>0,05), one exception that meiobenthic density in the station Rhi-c was significantly higher than in the station Rhi-a2 and Rhi-a3 (P<0,05) (fig. 3, D).

Fig. 2. Densities (mean ± sd) of meiobenthos (A), major benthic groups (B, C, D, E) and ratio Nematodes/Copepods (F) in dry and rainy seasons

Fig. 3. Densities (mean ± sd) of total meiobenthos in the Mud (A), Avi (B), Mix (C) Rhi (D) at different

stations in dry and rainy seasons

Meiobenthic density in the rainy season reduced so much to average 1630 ind/10 cm2, reduced 42 % of 2803 ind/10 cm2 in dry season. Density reduction with the highest percentage was 53 % of average density in dry season in Avicennia site. Result remained only average 1118 ind/10 cm2 in Avicennia site in rainy season. Assessment of meiobenthos in 4 sites in the rainy season showed densities in Mudflat and Mixed sites was significant higher than in Rhizophora and Avicennia sites (P<0,05) (fig. 2, A). Between stations in Mudflat site, meiobenthic density had no significant difference. In Avicennia site, Avi-b1 was significantly higher than all other stations, in the meantime the subtidal station Avi-c was significant lower than all others (P<0,05) (fig. 3, B). In Mixed site, between intertidal stations, Mix-b2 was significant higher than Mix-b3, and other intertidal stations were not significant difference. Change between intertidal and subtidal stations was significant (P<0,05) (fig. 3, C). In Rhizophora area, densities in Rhi-a1 and Rhi-b1 were significantly higher than in Rhi-b2 and Rhi-b3 (P<0,05), but not significant in Rhi-a2 and Rhi-a3 (P>0,05) (fig. 3, D).

Change of meiobenthic density in dry season and rainy season was significant difference among all sites. Densities of meiobenthos in dry season was significantly higher than in rainy season (P<0,05) (fig. 3, A). In Mudflat site, significant difference was in Mud-4 (P<0,05) (fig. 3, A). In other sites, significant differences were at stations Avi-a1 and Avi-b1 in Avicennia site, stations Mix-a1, Mix-a2 and Mix-c in Mixed site, stations Rhi-b2, Rhi-b3 and Rhi-c in Rhizophora site (P<0,05) (fig. 3, B; 3, C; 3, D).

III. 2. 2. Nematodes

In the dry season, result showed nematode percentage was 90,6 %, decreased in comparison with 87,2 % in the rainy season. The highest percentage of nematodes was remained in Mudflat site with 94,3 %. However, the lowest percentage was not in Avicennia site, but in Rhizophora site. On the other hand, to compare with nematodes in the rainy season, nematode density increased 35 %, reached average 2539 ind/10 cm2, mainly in Avicennia and Mudflat sites. Density of nematodes in Mudflat site was significantly higher than in Avicennia and Rhizophora sites (P<0,05). Density in Mixed site was higher than in Rhizophora, Avicennia sites and lower than in Mudflat site, however it did not varied significantly among sites (P>0,05) (fig. 2, B).

Within stations, there was not significant difference of nematode density between stations in Mudflat site (P>0,05) (fig. 2, E). In Avicennia site, density in Avi-a1 was significantly higher than in Avi-a2 and Avi-a3. In the opposite bank of the creek, Avi-b1 was also significantly higher than Avi-b2 and Avi-b3 (P<0,05). Density in subtidal station Avi-c was significantly lower than all intertidal stations (P<0,05) (fig. 4, B). In Mixed site, there was not significantly different between intertidal stations (P>0,05) (fig. 4, C). However in subtidal station Mix-c, density was significantly lower than other intertidal stations (P<0,05). Comparison of density in Rhizophora site, density in stations Rhi-a1, Rhi-b1, Rhi-c was significantly higher than in station Rhi-a2, Rhi-a3. Density in stations Rhi-b2, Rhi-b3 was lower than in station Rhi-b1, but the difference was not significant (P>0,05) (fig. 4, D).

Nematode density was also investigated in the rainy season. Result showed that nematode percentage reduced in comparison with the dry season and equivalent with the rainy season, was 87,2 % of the total meiobenthos. But percentages in different site forests were changed. Percentage was the highest in Mixed site and lowest in Rhizophora site. Nematode density reduced drastically about 44 % to compare with the dry season. Average nematode density was only 1421 ind/10 cm2 in the rainy season. Between 4 sites, densities in Mudflat and Mixed sites were significantly higher than in Rhizophora and Avicennia sites (P<0,05) (fig. 2, B). In Mudflat site, there was no significant different between stations (P>0,05) (fig. 4, A). In Avicennia site, nematode density in Avi-b1 was significantly higher than all others (P<0,05), Avi-c was significantly lower than almost of them except Avi-a2. Between stations in Mixed site, subtidal station Mix-c was significantly lower than all other stations, Mix-b2 was not significantly different from Mix-a1, Mix-a2, Mix-a3, Mix-b1 (P>0,05),

but significantly different from station Mix-b3 (P<0,05) (fig. 4, C). In Rhizophora site, Rhi-a1 and Rhi-b1 were significantly higher than Rhi-b2, Rhi-b3 and Rhi-c (P<0,05), but not significantly different from Rhi-a2 and Rhi-a3 (P>0,05) (fig. 4, D).

Between the dry season and the rainy season in, difference of nematode density was significant in all 4 sites (P<0,05) (fig. 2, B). In Mudflat site, difference between 2 seasons was significant at station Mud-4. In Avicennia site, significant difference between 2 seasons was at stations Avi-a1 and Avi-b1. In Mixed site, difference was significant at Mix-a2, Mix-b1 and Mix-c. In Rhizophora site, difference between dry and rainy seasons was significant at stations Rhi-b3 and Rhi-c (P<0,05) (fig. 4, A; 4, B; 4 C; 4, D).

Fig. 4. Densities (mean ± sd) of total meiobenthos in the Mud (A), Avi (B), Mix (C) Rhi (D) and nematodes in the Mud (E), Avi (F), Mix (G), Rhi (H) at different stations in dry and rainy seasons

III. 2. 3. Copepods and nauplii

In the dry season, result in Rachoc Creek showed copepods increased fairly and to be second abundance with average density 94 ind/10 cm2 and percentage 3,3 % of total meiobenthos. Copepods were the highest density in Rhizophora site (110 ind/10 cm2) and also the highest in percentage (4,4 % of total meiobenthos). Comparison of copepod density between 4 sites, there was not significant difference in dry season (P>0,05) (fig. 2,C).

Nauplii were the 4th abundance with average 1.3% of total meiobenthos. Nauplii density was the highest abundance 49 ind/10 cm2 (1,9 % of total meiobenthos) in Rhizophora site. However there was not significantly different among different sites (P>0,05) (fig. 2,D).

Copepod density in Rachoc Creek in the rainy season remained in the second abundance, but density reduced to average 73 ind/10 cm2. However, copepod percentage remained at level 4,5 % of total investigated meiobenthos. Among them, density was the highest in area of the Mudflat site with average 122 ind/10 cm2. Densities in Mudflat and Rhizophora sites were significantly higher than in Avicennia and Rhizophora sites (P<0,05) (fig. 3, C). In rainy season, nauplii were the third abundant group with 63 ind/10 cm2, occupied 3,9 % of total meiobenthos. The highest nauplii density was 121 ind/10 cm2 (5 %) in Mudflat site. In addition, density in Mudflat site was significantly higher than in other sites (P<0,05) (fig. 3, D). Difference of copepod densities between dry and

rainy seasons was significant in Mixed site only (P<0,05) (fig. 3, C). On the other hand, nauplii density had a significant difference in Mudflat site (P<0,05) (fig. 3, D).

III. 2. 4. Other less abundant groups

Some other groups as polychaetes, oligochaetes, acari and ostracods had a less abundance usually less than 1 % of total meiobenthos, but also showed their variations in different types of mangrove. In general, polychaete density reduced from Mudflat site to Rhizophora site in dry season. Difference between Rhizophora site and other sites was significant (P<0,05). In rainy season, oli-gochaete density changed a little, exception in Rhizophora site, density was significant higher than in dry season (P<0,05). However there was no significant difference among 4 sites in rainy season (P>0,05) (fig. 5, A).

Oligochaete densities in dry season changed among 4 sites but these were not significantly different (P>0.05). The same result was in rainy season. Comparison between 2 seasons, there was also no significant difference about density of oligochaetes (P>0,05) (fig. 5, B).

Ostracods in dry season showed densities in Mudflat and Avicennia sites were significantly higher than in Mixed site (P<0,05). But in rainy season, ostracod density reduced in all sites and there was no significant difference (P>0,05). Comparison in 2 seasons, ostracod densities in Mudflat, Avicennia and Rhizophora sites in dry season were significantly higher than in same sites in rainy season (P<0,05). In Mixed site change between 2 seasons was not significant (P>0,05) (fig. 5, D).

Fig. 5. Densities (mean ± sd) of less abundant groups oligochaetes (A), Polichaetes (B), Acari (C) and

Ostracods (D) in dry and rainy seasons

III. 3. Correlation with abiotic factors

The Table 2 showed a significant positive correlation between total meiobenthos, nematodes, copepods with water temperature (T°C) (P<0,05; P<0,01)). N/C ratio had a positive correlation with temperature also (P<0,05). On the other hand, total meiobenthos and nematode density were significant positive correlation with pH (P<0,05). In addition, polychaetes had significant positive correlation with oxygen in water (DO) (P<0,01). The abundances of meiobenthos and major meiobenthic groups were not significant correlation with salinity (NaCl) and turbidity (Tu). Other meioben-thic groups as nauplii, foraminifera, oligochaetes did not showed a significant correlation with temperature, oxygen in water, pH, salinity, and turbidity in this study.

81

Table 2

Correlation (r-value) of the abundance of total meiobenthos and meiobenthic groups, and the nematode/copepod ratio (N/C) with some physical variables at the sampling stations

Variable T (°C) DO (mg/l) pH NaCl (%o) Tu (mg/l)

Total meiobenthos 0,964** -0,238 0,833* 0,601 -0,259

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Nematodes 0,962** -0,233 0,827* 0,592 -0,244

Copepods 0,847* -0,363 0,749 0.638 -0,341

Nauplii 0,625 0,041 0,378 0,206 -0,007

Foraminifera 0,426 0,513 0,256 -0,103 -0,047

Polychaetes -0,332 0,942** -0,556 -0,807 0,414

Oligochaetes 0,388 0,636 0,014 -0,370 0,583

N/C ratio 0,892* 0,038 0,733 0,361 -0,020

Values with one star (*) are significant at P<0.05 Values with two stars (**) are significant at P<0,01

IV. Discussion

Composition and density of total meiobenthos

In a study meiobenthos in Malaysian mangrove, the result of Sasekumar (1994) seemed to be approximate with the result of Chinnadurai & Fernando (2007) when meiobenthic densities were 1109 ind/10 cm2 in Avicennia, 583 ind/10 cm2 in Rhizophora, and lowest 407 ind/10 cm2 in Bru-guiera forest. Present study shows the similarity with Vanhove et al. (1992). Based on all the samples taken from Rachoc Creek, meiobenthos densities were 1755 ind/10 cm2 in Avicennia, 2543 ind/10 cm2 in mixed forest of Avicennia and Rhizophora, 1947 ind/10 cm2 in Rhizophora. It seems that Rhizophora in Can Gio mangrove may be more attractive to meiobenthos than Avicennia. In addition, the highest densities of meiobenthos in mixed forest of Avicennia and Rhizophora suggested that mangroves with multi-plant species can create a habitat that more appropriate for development of meiobenthos than mono plant species mangroves.

Abundance of major meiobenthic groups

Normally, nematodes occupied over 80 % of total meiobenthos, sometimes up till 95-99 % Vanhove et al., 1992, Olafsson (1995, 2000); Khalil, 2001; Netto & Gallucci, 2003; Armenteros et al., 2006; Chinnadurai & Fernando, 2007). Nematodes seem to be less important in a study from Australian mangroves with 27-31 % (Alongi, 1987a), and in Cuba mangroves with percentages 35-61% (Lalana-Rueda & Gosselck, 1986). Nematodes are also recorded to be the most abundant taxa in the present study. The average nematode percentages were from 81,1-94,3 %. Among the three types of mangroves in Rachoc Creek, the nematode percentages and densities were generally higher in mud flat site and mixed forest site than Avicennia and Rhizophora sites. Between the two seasons, Rachoc Creek showed that nematode percentages and densities in dry season were higher than in rainy season. Heavy rains could disturb sediment surface and influence to ratio and density of meiobenthos as well as nematodes. Dry season in Can Gio created a more appropriate environmental condition for nematode development than rainy season. Our result showed that copepods were the second abundance in most study stations. Copeppod percentages showed gradual change from Rhizophora sites (6,7 %), to mixed forest Avicennia site and Rhizophora sites (2,5 %). Among three types of forest, copepod percentages were higher in Avicennia and Rhizophora sites than in Mixed forest site. The difference was clearer in rainy season. The reason can be from forest structure. Plantation covers and number of tree in Avicennia and Rhizophora forests are much smaller than mixed forest. These could influence to sediment surface of forest types and subsequently change copepod distribution. Vanhove et al. (1992) noted low copepod percentages in silty/muddy

sediment suggested this taxon is more related to coarser grain texture. In addition, copepods and epsilonematid nematodes do not withstand high silt fraction. Copepods are report as one of the most sensitive taxon is sensitive for oxygen decrease and usually restricted inoccurrence in oxic condition (Coull & Chandler, 1992).

In present study, nematode and copepod densities possitively correlated with temperature. Nematode density also possitive correlated with pH and polichaetes possitively correlated with dissolved oxygen. Other meiobenthic group had no correlation with abiotic factors. However, Ólafsson (1995) pointed that lack of significant correlations between environmental factors and meiofauna taxa does not mean that these factors were not contributing to the density variations observed. They may indeed control the population densities of the major taxa differently and in different proportion at the various stations. An experiment approach when the factor of interest can be manipulated while fluctuations in all other variables kept to minimum may be more appropriate than simple correlation analyses, in evaluating the importance of community control mechanisms.

Acknowledgements. This research was supported by the Vietnam National Scientific Basic Programme for Biodiversity (DA 47), under Project VAST.BA.12/16-19.

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