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FIG. 2. — Galathowenia minuta n in Review of Oweniidae Rioja, 1917 (Annelida, Palaeoannelida) from Malaysia, with a description of two new species and a key to South China Sea species
FIG. 2. — Galathowenia minuta n. sp. holotype, UMTAnn 2184: A, anterior end, dorsal view; B, posterior end, lateral view; C, grain sand cemented tube; midbody part; D, grain sand cemented tube; posterior end; E, posterior chaetigers with long capillary chaeta; lateral view; F, transverse rows of hooked uncini; mid body; G, hooked uncini in oblique position mid body. Abbreviation: S, segment. Scale bars: A, B, 200 µm; C, D, E, 100 µm; F, G, 10 µm.
FIG. 3. — Owenia unipinnata n in Review of Oweniidae Rioja, 1917 (Annelida, Palaeoannelida) from Malaysia, with a description of two new species and a key to South China Sea species
FIG. 3. — Owenia unipinnata n. sp. holotype, UMTAnn 2186: A, complete full body of individual, with posterior part slightly bend towards the body; B, anterior end, ventral view, stained using rose bengal (microscopic image) with schematic diagram (completed with numbered arrows) of tentacular crown showing simple solitary ramification; C, anterior end, ventral (left) and dorsal (right) views, stained using methylene blue; D, flattened posterior end with broken lobes and gold coloured notochaeta; E, capillary chaeta with densely packed scales; F, hooked uncini with left teeth bend towards the right teeth; G, tori almost encircles the body; H, overlapping quartz grains and shell fragments of tube. Number 1, 2, 3, indicate the number of ramifications. Scale bars: A, 1 mm; B, C, D, G, H, 100 µm; E, F, 5 µm.
FIG. 1 in Review of Oweniidae Rioja, 1917 (Annelida, Palaeoannelida) from Malaysia, with a description of two new species and a key to South China Sea species
FIG. 1. — Sampling positions along the coastal defence structure areas of Kuala Nerus, Terengganu: station 1, groyne (1.1: 5°23'25.7"N, 103°06'59.9"E; 1.2: 5°23'47.5"N, 103°07'04.3"E; 1.3: 5°23'58.0"N, 103°06'26.6"E); station 2, semi-enclosed jetty type breakwater (Inside lagoon: 5°24'08.2"N, 103°06'06.6"E; Outside lagoon: 5°24'12.6"N, 103°06'15.5"E); station 3, parallel breakwater without tombolo (3.1: 5°24'21.6"N, 103°05'56.7"E; 3.2: 5°24'32.4"N, 103°05'54.2"E; 3.3: 5°24'32.0"N, 103°05'45.7"E); station 4, Parallel breakwater with tombolo (4.1: 5°24'38.2"N, 103°05'39.4"E; 4.2: 5°24'45.9"N, 103°05'40.3"E; 4.3: 5°24'42.9"N, 103°05'33.4"E); station 5, Batu Rakit (5°27'09.0"N, 103°02'58.4"E).
Table 3 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea
<p><b>Table 3.</b> Measurements of <i>Neohexostoma gymnosardae</i> n. sp. from <i>Gymnosarda unicolor</i> from the South China Sea, and <i>Neohexostoma</i> spp.</p><table><tbody><tr><th></th><th><i>N. gymnosardae</i></th><th><i>N. mochimae N. kawakawa</i></th><th><i>N. thunninae</i></th><th><i>N. euthynni</i></th><th><i>N. extensicaudum N. robustum</i></th><th><i>N. pricei</i></th></tr></tbody><tbody><tr><th></th><td>n. sp.</td><td>Fuentes-Zambrano,</td><td>Yamaguti,</td><td>(Parona &</td><td>(Meserve,</td><td>(Dawes, 1940)</td><td>Price, 1961</td><td>(Koratha,</td></tr><tr><th></th><td></td><td>1997</td><td>1968</td><td>Perugia,</td><td>1938)</td><td></td><td></td><td>1955)</td></tr><tr><th></th><td></td><td></td><td></td><td>1889)</td><td></td><td></td><td></td><td></td></tr><tr><th>Hosts <i>Gymnosarda unicolor</i></th><td><i>Auxis thazard</i></td><td><i>Euthynnus</i></td><td><i>Thynnus</i></td><td><i>Euthynnus alleteratus</i></td><td><i>Thunnus thynnus Thunnus obesus Sarda sarda</i></td></tr><tr><th></th><td></td><td></td><td><i>yaito</i></td><td><i>thunninae</i></td><td>[<i>Euthynnus lineatus</i>]</td><td></td><td><i>(Parathynnus</i></td><td></td></tr><tr><th></th><td></td><td></td><td><i>Neothunnuus</i></td><td></td><td></td><td></td><td><i>sibi)</i></td><td></td></tr><tr><th></th><td></td><td></td><td><i>macropterus</i></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Locality</th><td>South China Sea, P.</td><td>Venezuela, A.</td><td>Hawaii, P.</td><td>Italy, M.</td><td>Galapagos Islands, P.</td><td>English</td><td>Tropical Pacific Texas, A.</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>[Baja California, P.]</td><td>Channel, A.</td><td></td><td></td></tr><tr><th>Source</th><td>Present study</td><td>[35]</td><td>[34]</td><td>[24, 25]</td><td>[20] [21]</td><td>[7]</td><td>[26]</td><td>[17]</td></tr><tr><th>Body length 9660–18800 (13827)</th><td>4444–6166 (5093)</td><td>4900–8400</td><td>11,000–12,000</td><td>5853 [3570–5850]</td><td>11,000</td><td>17,000</td><td>4500</td></tr><tr><th>Body width</th><td>2875–5375(3847)</td><td>874–1160 (1011)</td><td>70–180</td><td>2000</td><td>953 [740–950]</td><td>3300</td><td>4000–4700</td><td>400–850</td></tr><tr><th>Haptor length 1172–1810 (1 446)</th><td>665–1140 (903)</td><td></td><td></td><td>953</td><td></td><td></td><td>440</td></tr><tr><th>Haptor width</th><td>1369–2582 (1827)</td><td>1273–1615 (1444)</td><td>1200–1550</td><td>1500</td><td>1300</td><td></td><td></td><td>750–850</td></tr><tr><th>Clamps</th><td>1st pair: 275–506</td><td>Anterior 3 clamps:</td><td>224–370</td><td>1st pairs:</td><td>203 × 339 [Anterior 3</td><td>0.067**</td><td>1st pair:</td><td>Anterior two pairs:</td></tr><tr><th></th><td>× 505–697</td><td>122–209</td><td>× 200–230</td><td>275 × 220</td><td>clamps:</td><td></td><td>500 × 750</td><td>500 × 340</td></tr><tr><th></th><td>(415 × 594)</td><td>× 200–315</td><td></td><td></td><td>153–255 × 221–403,</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>(164 × 250)</td><td></td><td></td><td>posterior-most pair:</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>156–238 × 194–332]</td><td></td><td></td><td></td></tr><tr><th></th><td>2nd pair: 327–477</td><td>Posterior clamp:</td><td></td><td>2nd pairs:</td><td></td><td>0.030***</td><td>2nd pair:</td><td>3rd pair:</td></tr><tr><th></th><td>× 577–713</td><td>94–177 ×</td><td></td><td>225 × 180</td><td></td><td></td><td>600 × 850</td><td>460 × 340</td></tr><tr><th></th><td>(395 × 620)</td><td>117–198 (126 × 166)</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>3rd pair: 302–455</td><td></td><td></td><td></td><td></td><td></td><td>3rd pair:</td><td>4th pair: 375 × 300</td></tr><tr><th></th><td>× 475–624</td><td></td><td></td><td></td><td></td><td></td><td>500 × 670</td><td></td></tr><tr><th></th><td>(376 × 587)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>4th pair: 233–358</td><td></td><td></td><td></td><td></td><td></td><td>4th pair:</td><td></td></tr><tr><th></th><td>× 389–496</td><td></td><td></td><td></td><td></td><td></td><td>350 × 500</td><td></td></tr><tr><th></th><td>(316 × 447)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Oral sucker</th><td>62–99 ×</td><td>29–30 ×</td><td>28–45*</td><td></td><td>56 × 40[27–56 × 24–40]</td><td>– × 100</td><td></td><td>40 × 30</td></tr><tr><th></th><td>51–102 (83 × 70)</td><td>28–30(30 × 29)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Pharynx</th><td>63–93 ×</td><td>40–13 ×</td><td>40–58 ×</td><td></td><td>[44–68 × 26–36]</td><td>100 × 70</td><td></td><td>75 × 45</td></tr><tr><th></th><td>49–58 (82 × 55)</td><td>24–29 (42 × 26)</td><td>23–35</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Vagina</th><td>244–359 ×</td><td>10–40 (35)*</td><td>Pads: 60–80</td><td>54*</td><td></td><td>600 × 350</td><td></td><td>Right pad: 55 × 24</td></tr><tr><th>191–250 (302 × 221)</th><td></td><td>× 20–30</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>Left pad: 70 × 24</td></tr><tr><th>Genital atrium 92–321 ×</th><td></td><td>40–70*</td><td></td><td></td><td>600 × 300</td><td></td><td></td></tr><tr><th>112–348 (225 × 228)</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Large anchor</th><td>43–57 (50)</td><td>34–90(64)</td><td>85–105</td><td>135</td><td>68 [85–120]</td><td>75</td><td>100</td><td>145</td></tr><tr><th>Small anchor</th><td>39–42(41)</td><td>20–31(25)</td><td>20–40</td><td>45</td><td>34 [24 – 34]</td><td>15</td><td>40</td><td></td></tr><tr><th>Eggs</th><td>125–193 ×</td><td>182–196 ×</td><td>180–260 ×</td><td>270 × 91</td><td>168–203 × 72–80</td><td>250 × 150</td><td>220 × 110</td><td></td></tr><tr><th></th><td>91–137 (156 × 114)</td><td>74 (196 × 74)</td><td>70–160</td><td></td><td>[103–221 × 44–105]</td><td></td><td></td><td></td></tr><tr><th>Egg filaments 411–719 (518)</th><td></td><td>up to 200</td><td></td><td>100 [anterior: 100–179,</td><td>250</td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>posterior: 100–161]</td><td></td><td></td><td></td></tr><tr><th>Testes number 185–246</th><td>30–35</td><td>13–35</td><td></td><td>26 [32 –40]</td><td></td><td>Numerous</td><td></td></tr></tbody></table><p>The width of the body given for <i>N. extensicaudum</i> is that of the third region. The data for <i>N. euthynni</i> in square brackets are from Millemann (1956) [21].</p><p><sup>*</sup> Diameter. <sup>**</sup> Ratio large clamp/body length. <sup>***</sup> Ratio small clamp/body length. A., Atlantic Ocean. M., Mediterranean Sea. P., Pacific Ocean.</p>
Table 1 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea
<p><b>Table 1.</b> Species of monogeneans used in the molecular analyses.</p><table><tbody><tr><th>Species</th><th>Family</th><th>Accession No.</th><th>Reference</th></tr></tbody><tbody><tr><th><i>Neohexostoma gymnosardae</i> n. sp.</th><td>Hexostomatidae</td><td>MN242399</td><td>Present study</td></tr><tr><th><i>Hexostoma thynni</i> (Delaroche, 1811) Rafinesque, 1815</th><td>Hexostomatidae</td><td>EF653383</td><td>[1]</td></tr><tr><th><i>Diplostamenides sciaenae</i> (Goto, 1894) Mamaev, 1986</th><td>Microcotylidae</td><td>FJ432589</td><td>Direct submission</td></tr><tr><th><i>“ Cynoscionicola branquialis ”</i></th><td>Microcotylidae</td><td>AF382050</td><td>[23]</td></tr><tr><th><i>Diclidophora denticulata</i> (Olsson, 1876) Price, 1943</th><td>Diclidophoridae</td><td>AF382047</td><td>[23]</td></tr><tr><th><i>Urocotyle nibae</i> Zhang & Xiao in Zhang, Yang & Liu, 2001</th><td>Diclidophoridae</td><td>FJ432588</td><td>Direct Submission</td></tr><tr><th><i>Gotocotyla bivaginalis</i> (Ramalingam, 1961) Rohde, 1976</th><td>Gotocotylidae</td><td>AF382039</td><td>[23]</td></tr><tr><th><i>Gotocotyla secunda</i> (Tripathi, 1954)</th><td>Gotocotylidae</td><td>AF382040</td><td>[23]</td></tr><tr><th><i>Pseudohexabothrium taeniurae</i> Agrawal, Chisholm & Whittington, 1996</th><td>Hexabothriidae</td><td>AF382035</td><td>[23]</td></tr><tr><th><i>Hypanocotyle bullardi</i> Chero, Cruces, Sáez, Camargo, Santos & Luque, 2018</th><td>Hexabothriidae</td><td>MG591249</td><td>[5]</td></tr><tr><th><i>Polystoma gallieni</i> Price, 1938</th><td>Polystomatidae</td><td>AF382064</td><td>Direct Submission</td></tr></tbody></table><p>“ <i>Cynoscionicola branquialis</i> ” was accepted as “ <i>Cynoscionicola branchialis</i> ”, but in a status of taxon inquirendum. <i>Gotocotyla secunda</i> (Tripathi, 1954) was accepted as <i>Gotocotyla acanthura</i> (Parona & Perugia, 1896) Meserve, 1938.</p>
The in situ Mg/Ca ratios of planktonic foraminifera shells in the northeastern South China Sea: an attempt to get efficient and reliable proxies
<p>Planktonic foraminifera are one of the important carrier<span>s</span> of the physico-chemical environments. Nowadays, the development of <em>in situ</em> microanalysis technology provides a new opportunity for further understanding the distribution and variation of trace element concentrations in foraminifera shells. In this study, we focus on the <em>in situ</em> Mg/Ca ratios in four planktonic foraminifera shells from the surface sediments of the northeastern slope of the South China Sea (SCS). The results of electron microprobe mapping indicate that <em>G. ruber</em> had periodic bands of high Mg contents and Mg/Ca ratios, consistent with the results of <span>LA-ICP-MS.</span> In contrast, <em>N. dutertrei</em>, <em>P. obliquiloculata,</em> and <em>G.inflata</em> had thick calcite layer with low Mg contents and Mg/Ca ratios. The Mg/Ca ratios of shells may be attributed to symbionts, but the physiological regulation may also have some contributions. Meanwhile, contaminants may lead to the relatively higher Mg/Ca ratios. Therefore, the large Mg/Ca variations in foraminifera shells are not only affected by the surrounding seawater temperature but also constrained by other factors. At last, we employed this method to reconstruct the Mg/Ca-SST in the northeastern SCS over the past ~3000 years. The similar trend to the previous SST records proves that this method is reliable. We hope that this method can be widely applied in the future due to the efficient, fast, and high spatial resolution with small sample amounts.</p>
Linked collectors and determiners for: The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata).
Natural history specimen data linked to collectors and determiners held within, "The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a>. Formatted as a Frictionless Data package.
Figure 5 in Three new species of free-living marine nematodes from the Bohai Sea and Yellow Sea, China
Figure 5. Parodontophora wuleidaowanensis sp. nov. (a) Lateral view of male head-end; (b) lateral view of female head-end; (c) tail of male; (d) tail of female. Scale bar: 20 mm.
Figure 4 in Three new species of free-living marine nematodes from the Bohai Sea and Yellow Sea, China
Figure 4. Parodontophora deltensis sp. nov. (a) Lateral view of male buccal cavity (400×); (b) lateral view of male anterior end, showing amphids (400×); (c) lateral view of male tail, showing spicules and gubernacula with apophyses (200×).
Figure 3 in Three new species of free-living marine nematodes from the Bohai Sea and Yellow Sea, China
Figure 3. Parodontophora deltensis sp. nov. (a) Lateral view of male head-end; (b) lateral view of male tail; (c) lateral view of male copulatory apparatus; (d) lateral view of female head-end; (e) tail of female. Scale bar: 20 mm (a, c, d); 50 mm (b, e).
Figure 2 in Three new species of free-living marine nematodes from the Bohai Sea and Yellow Sea, China
Figure 2. Paranticoma tricerviseta sp. nov. (a) Lateral view of male anterior end, showing cervical setae (1000×); (b) lateral view of spicules (400×); (c) lateral view of male tail (200×); (d) lateral view of conical part of male tail, showing subventral setae (400×).
Figure 1 in Three new species of free-living marine nematodes from the Bohai Sea and Yellow Sea, China
Figure 1. Paranticoma tricerviseta sp. nov. (a) Lateral view of male head-end; (b) lateral view of female head-end; (c) lateral view of male copulatory apparatus and ventral-middle setae behind anus in the tail; (d) last part of the tail. Scale bar: 20 mm.
Figures 27–38 in Redescription of Pseudovorticella cylindrica (Dons, 1915) nov. comb. and Zoothamnium hiketes Precht, 1935, two poorly defined marine peritrichs (Ciliophora: Peritrichia) from the north China Sea
Figures 27–38. Photomicrographs of Zoothamnium hiketes from life (27–31), after protargol (32–34, 36–38) and silver nitrate impregnation (35). (27) Colony at low magnification. (28) Detail of stalk, arrowheads showing rodshaped bacteria on stalk surface. (29) Zooids at 400× magnification. (30) Varieties of body shape, arrows indicate contractile vacuole. (31) Lateral view of a zooid at 1250× magnification, showing the pellicle striations. (32) Arrows mark aboral ciliary wreath. (33) Oral apparatus, indicating three peniculi (P1–3). (34) To show the branching form. (35) General silverline system, arrow marks the aboral ciliary wreath. (36) Arrow showing the distal fragment of oral apparatus. (37) General appearance, to mark aboral ciliary wreath (arrowheads). (38) To show epistomial membrane (arrow) and germinal kinety (double arrowhead). P1–3, peniculi 1–3. Scale bars: 200 mm (27); 50 mm (29); 70 mm (30); 100 mm (34).
Figures 45–55 in Redescription of Pseudovorticella cylindrica (Dons, 1915) nov. comb. and Zoothamnium hiketes Precht, 1935, two poorly defined marine peritrichs (Ciliophora: Peritrichia) from the north China Sea
Figures 45–55. Comparison of some morphotypes closely related to Zoothamnium hiketes. (45) Zoothamnium cienkowskii (from Kahl 1935). (46, 47) Zoothamnium affine (from Song 1991b). (48, 49) Zoothamnium maximum (from Ji and Song 2004). (50, 51) Zoothamnium duplicatum (from Ji et al. 2005). (52, 53) Zoothamnopsis mengi (from Song 1997). (54, 55) Zoothamnopsis sinica (from Ji and Song 2004). Scale bars: 50 mm (45, 46, 48, 50, 52, 54); 100 mm (47, 51, 53); 300 mm (49, 55).
Figures 9–18 in Redescription of Pseudovorticella cylindrica (Dons, 1915) nov. comb. and Zoothamnium hiketes Precht, 1935, two poorly defined marine peritrichs (Ciliophora: Peritrichia) from the north China Sea
Figures 9–18. Photomicrographs of Pseudovorticella cylindrica from life (9–11, 13), after protargol (12, 15, 17, 18) and silver nitrate impregnation (14, 16). (9) A fully extended zooid at low magnification. (10) Detail of stalk, arrows show thecoplasmic granules in spasmoneme. (11) Zooids at low magnification. (12) Arrow indicates epistomial membrane. (13) A contracted zooid at low magnification. (14, 16) Silverline system, showing reticulate meshes, double arrowhead marks aboral ciliary wreath. (15) Anterior end of zooid showing peniculi 1–3. (17) Lateral view, showing aboral ciliary wreath (arrowheads). (18) Apical view, showing polykinety and haplokinety. H, haplokinety; P1–3, peniculi 1–3; Po, polykinety. Scale bars: 120 mm (9); 200 mm (11); 60 mm (13).
Figures 19–26 in Redescription of Pseudovorticella cylindrica (Dons, 1915) nov. comb. and Zoothamnium hiketes Precht, 1935, two poorly defined marine peritrichs (Ciliophora: Peritrichia) from the north China Sea
Figures 19–26. Morphology of Zoothamnium hiketes from life (19–23), after protargol (24, 25) and silver nitrate impregnation (26). (19) General view of a typical zooid. (20) Showing varieties of body shape and macronucleus. (21) Detail of stalk, arrowheads show many rod-shaped bacteria on stalk surface. (22) Zoothamnium hiketes (from Precht 1935). (23) Colony form. (24) Detail of the three oral peniculi, arrows mark separated upper end of the outer two rows in P2. (25) Oral infraciliature, arrow notes epistomial membrane, double arrowhead indicates the oral distal fragment. (26) Silverline system. ACW, aboral ciliary wreath; G, germinal kinety; H, haplokinety; P1–3, peniculi 1–3; Po, polykinety. Bars: 30 mm (19); 20 mm (21, 22a); 100 mm (22b); 150 mm (23).
Figures 1–8 in Redescription of Pseudovorticella cylindrica (Dons, 1915) nov. comb. and Zoothamnium hiketes Precht, 1935, two poorly defined marine peritrichs (Ciliophora: Peritrichia) from the north China Sea
Figures 1–8. Morphology of Pseudovorticella cylindrica from life (1–5), after protargol (6, 7) and silver nitrate impregnation (8). (1) A typical zooid. (2) Detail of stalk, arrows to show conspicuous thecoplasmic granules in spasmoneme. (3) From Dons (1915) (called Vorticella cylindrica). (4) From Song (1991a) (called Vorticella cylindrica). (5) Typical zooids at low magnification. (6) Buccal apparatus, arrow indicates epistomial membrane. (7) Variable shape of macronucleus. (8) Silverline system. ACW, aboral ciliary wreath; G, germinal kinety; H, haplokinety; P1–3, peniculi 1–3; PD, peristomial disc; PL, peristomial lip; Po, polykinety; Sc, scopula; Spa, spasmoneme. Scale bars: 30 mm (1); 20 mm (4); 50 mm (5).
Fig. 4 in Patterns In Community Structure Of Trawl Catches Along Coastal Area Of The South China Sea
Fig. 4. Cluster dendogram of abundance data for preference of 30 dominant fishes collected bimonthly (a) at different study sites and (b) in different months off Pattani and Narathiwat coasts between Nov.2005 and Jul.2007.
Fig. 3 in Patterns In Community Structure Of Trawl Catches Along Coastal Area Of The South China Sea
Fig. 3. Cluster dendogram of abundance data for each fish samples collected bimonthly (a) at four different zones and (b) in different months off Pattani and Narathiwat coasts between Nov.2005 and Jul.2000
Fig. 5 in Patterns In Community Structure Of Trawl Catches Along Coastal Area Of The South China Sea
Fig. 5. Cluster dendogram of benthic organisms' abundance data collected off Pattani and Narathiwat coasts between Nov.2005 and Jul.2007.
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