Figure 1

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Figure 6

Differences in abiotic parameters of seawater (temperature – T and salinity – S) as well as sediment [pH, electrical conductivity – EC (mS cm−1); total organic carbon – TOC; and MD – mean grain size] observed at different sites along the Saudi Arabian coast of the Red Sea
| Site | Seawater | Sediment | ||||||
|---|---|---|---|---|---|---|---|---|
| T (°C) | S (PSU) | pH | EC (mS cm−1) | TOC (%) | MD (μm) | Sediment type | Sorting Index | |
| I | 28.9 | 38.56 | 8 | 6.9 | 3.5 | 353 | medium sand | poorly sorted |
| II | 28.5 | 43.1 | 8 | 5.3 | 3 | 296 | medium sand | poorly sorted |
| III | 31.1 | 40.3 | 7.05 | 22 | 3 | 356 | medium sand | poorly sorted |
| IV | 27.9 | 38.2 | 7.77 | 6.79 | 1 | 96 | very fine sand | moderately sorted |
| V | 28.9 | 40.1 | 7.6 | 10.26 | 3.7 | 208 | fine sand | poorly sorted |
| VI | 29.4 | 42.9 | 7.91 | 8.09 | 2.9 | 451 | medium sand | poorly sorted |
| VII | 28.7 | 41.5 | 6.75 | 9.95 | 3.3 | 243 | fine sand | poorly sorted |
| VIII | 28.5 | 39.3 | 7.45 | 10.1 | 2.5 | 229 | fine sand | poorly sorted |
| IX | 32.1 | 43.6 | 7.3 | 9.9 | 3 | 150 | fine sand | poorly sorted |
| X | 32.4 | 40.1 | 7.78 | 7.31 | 3.5 | 441 | medium sand | poorly sorted |
| XI | 29.3 | 43.1 | 7.82 | 10.1 | 1.8 | 156 | fine sand | poorly sorted |
| XII | 28.1 | 41.3 | 7.65 | 10.19 | 2.8 | 366 | medium sand | poorly sorted |
| XIII | 29.8 | 41.1 | 7.91 | 8.9 | 2 | 350 | medium sand | poorly sorted |
| XIV | 31.5 | 41.1 | 8.01 | 2.31 | 1.1 | 747 | coarse sand | moderately sorted |
| XV | 31.2 | 42.1 | 7.61 | 11.65 | 1.9 | 183 | fine sand | poorly sorted |
| XVI | 31.1 | 41.1 | 7.95 | 10.19 | 1.9 | 232 | fine sand | moderately sorted |
| XVII | 33.2 | 41.3 | 7.87 | 6.79 | 1.3 | 224 | fine sand | moderately sorted |
| XVIII | 36.2 | 42.1 | 7.91 | 6.49 | 1.7 | 197 | fine sand | poorly sorted |
| XIX | 35.1 | 43.5 | 7.85 | 6.8 | 1.6 | 249 | fine sand | poorly sorted |
| XX | 29.2 | 40.8 | 8.08 | 7.76 | 2.5 | 232 | fine sand | poorly sorted |
Total count, relative abundance (%) and feeding types of different nematode genera recorded in mangrove sediments along the Saudi Arabian coast of the Red Sea_ 1A – selective deposit feeders; 1B – non-selective deposit feeders; 2A – epigrowth feeders; 2B – predators/omnivores
| Order | Family | Genus | Total count | Relative abundance (%) | Feeding type |
|---|---|---|---|---|---|
| Enoplida | Ironidae | Syringolaimus | 1155 | 14.0 | 2a |
| Dolicholaimus | 86 | 1.0 | 2b | ||
| Oxystominidae | Halalaimus | 1336 | 16.2 | 1a | |
| Oncholaimidae | Viscosia | 85 | 1.0 | 2b | |
| Oncholaimus | 71 | 0.9 | 2b | ||
| Tripyloididae | Bathylaimus | 40 | 0.5 | 1b | |
| Aegialoalaimdae | Aegialoalaimus | 59 | 0.7 | 1a | |
| Chromadorida | Chromadoridae | Spilophorella | 91 | 1.1 | 2a |
| Metachromadora | 63 | 0.8 | 2a | ||
| Cyatholaimidae | Paralongicyatholaimus | 135 | 1.6 | 2a | |
| Selachinematidae | Synonochium | 49 | 0.6 | 2b | |
| Desmodoridae | Desmodora | 745 | 9.0 | 2a | |
| Molgolaimus | 29 | 0.4 | 2a | ||
| Spirina | 447 | 5.4 | 2a | ||
| Leptolaimidae | Leptolaimus | 48 | 0.6 | 1a | |
| Microlaimidae | Microlaimus | 1442 | 17.4 | 2a | |
| Bolbolaimus | 198 | 2.4 | 2a | ||
| Desmoscolecidae | Desmosolozenia | 17 | 0.2 | 1a | |
| Haliplectidae | Haliplectus | 63 | 0.8 | 1a | |
| Monhysterida | Xyalidae | Stylotheristus | 49 | 0.6 | 1b |
| Theristus | 196 | 2.4 | 1a | ||
| Paramonhystrea | 201 | 2.4 | 1b | ||
| Daptonema | 722 | 8.7 | 1b | ||
| Linhomoeidae | Metalinhomoeus | 90 | 1.1 | 1b | |
| Terschellingia | 849 | 10.3 | 1a |
Meiofaunal abundance determined in different mangrove sediments worldwide (mean values given in parentheses)
| Area/Country | Densities (ind. 10 cm−2) | References |
|---|---|---|
| Minimum–Maximum (mean) | ||
| Hunter River, south-eastern Australia | 63–12057 (225) | Hodda & Nicholas (1985) |
| Hunter River, south-eastern Australia | 1–9596 (110) | Hodda & Nicholas (1986) |
| Northeastern Australia | 57–2454 | Alongi (1987a,b) |
| Mangrove mudflats, Australia In the top 1 cm of Av. marina sediment; | 470–5000 (1830) | Nicholas et al. (1991) |
| Barwon estuary, Victoria, Australia | 250–8622 (2170) | Gwyther (2000) |
| Mngazana estuary, South Africa | 84–530 (246) | Dye (1983 a) |
| New Caledonia | 70–5137 | Della Patrona et al. (2016) |
| West and east coast of Zanzibar, Africa | 205–5263 (1493) | Ólafsson (1995) |
| West and east coast of Zanzibar, Africa | 271–656 | Ólafsson et al. (2000) |
| Gazi Bay, Kenya, Africa | 1986–6707 | Vanhove et al. (1992) |
| Island of Santa Catarina, South Brazil | 77–1589 (448) | Netto & Galucci (2003) |
| South Cuba | 36–245 | Lalana-Rueda & Gosselck (1980) |
| Gulf of Batabano, Cuba | 5–594 (109) | Armenteros et al. (2006) |
| West coast of Malaysia | 407–1109 (700) | Sasekumar (1994) |
| Southeast coast of India | 234–890 | Chinnadurai & Fernando (2007) |
| Northern Red Sea, Egypt | (343) | Pusceddu et al. (2014) |
| Sudanese coast of the Red Sea Intact mangrove | (288) | Sabeel (2015) |
| Western side of the Red Sea, Egypt | 18–193 (109) | El-Serehy et al. (2015) |
| Saudi Arabian coast of the Red Sea | 119–1380 (643) | Present study |
Biodiversity indices of nematodes determined for different sites along the Saudi Arabian coast of the Red Sea: the total number of genera (S), richness (D), Pielou’s evenness index (J’) and Shannon-Wiener index (H’)
| Site | S | d | J’ | H’ (log) |
|---|---|---|---|---|
| I | 2 | 0.27 | 0.95 | 0.66 |
| II | 1 | 0.00 | 0.00 | 0.00 |
| III | 1 | 0.00 | 0.00 | 0.00 |
| IV | 3 | 0.63 | 1.00 | 1.10 |
| V | 2 | 0.35 | 0.95 | 0.66 |
| VI | 3 | 0.54 | 1.00 | 1.10 |
| VII | 3 | 0.59 | 0.99 | 1.09 |
| VIII | 1 | 0.00 | 0.00 | 0.00 |
| IX | 2 | 0.34 | 0.97 | 0.67 |
| X | 4 | 0.91 | 0.98 | 1.36 |
| XI | 2 | 0.32 | 0.97 | 0.68 |
| XII | 10 | 1.96 | 0.98 | 2.26 |
| XIII | 2 | 0.31 | 0.99 | 0.69 |
| XIV | 3 | 0.55 | 0.98 | 1.08 |
| XV | 2 | 0.37 | 0.94 | 0.65 |
| XVI | 4 | 0.80 | 0.91 | 1.26 |
| XVII | 11 | 2.15 | 0.98 | 2.36 |
| XVIII | 10 | 2.00 | 0.98 | 2.25 |
| XIX | 5 | 1.03 | 0.99 | 1.59 |
| XX | 2 | 0.34 | 0.99 | 0.69 |
Nematode abundance (mean in parenthesis), percentage of total meiofauna, richness and dominant genera recorded in different mangrove sediments worldwide
| References | Area/Country | Densities (ind. 10 cm−2) Minimum–Maximum (mean) | % of total meiofauna | Number of families | Number of genera |
|---|---|---|---|---|---|
| Hodda & Nicholas (1985) | Hunter River, south-eastern Australia | 63–11892 | 87–100 | 23 | 55 |
| Alongi (1987b) | Cape York, north-east Australia | 3–987 | – | (205 sp.) | |
| Nicholas et al. (1991) In the top 1 cm of Av. marina sediment | Mangrove mudflats, Australia | 113–451 | – | 26 | 38 |
| Dye (1983a) | Mngazana estuary, South Africa | 62–411 | 80.4 | – | – |
| Vanhove et al. (1992) | Gazi bay, Kenya | – | 54–95 | – | – |
| Ólafsson (1995) | West-east coast of Zanzibar, Africa | 131–5210 | 64-99 | 30 | 94 |
| Ólafsson et al. (2000) | West-east coast of Zanzibar, Africa | 271–656 | 58–87 | 13 | 28 |
| Netto & Galucci (2003) | Island of Santa Catarina, South Brazil | 196–811 | 85–94 | 28 | 86 |
| Pinto et al. (2013) | Pernambuco state, Northeastern Brazil | – | – | 25 | 73 |
| Armenteros et al. (2006) | Gulf of Batabano, Cuba | 5–591 (104) | 33–100 (88) | – | – |
| Ali et al. (1983) | Bay of Bengal, India | 35–280 | 50–67 | – | – |
| Chinnadurai & Fernando (2007) | Southeast coast of India | 234–890 | 86–93 | 20 | 36 |
| Bhadury et al. (2015) | Central west coast of India | – | – | 13 | 20 |
| Ansari & Bhadury (2017) | Sundarbans, India-Bangladesh | – | – | 29 | 84 |
| Somerfield et al. (1988) | North-western coast of Malaysia | (122) | – | 32 | 85 |
| Sasekumar (1994) | West coast of Malaysia | 374–885 | 80–93 | – | 17 |
| Sabeel (2015) | Sudanese coast, Red Sea | 10–370 | 40–98 | 20 | 35 |
| El-Serehy et al. (2015) | Western side of the Red Sea, Egypt | 8–162 (73) | 42(–6784) | – | – |
| Present study | Saudi Arabian coast of the Red Sea | 72–1100 | 29–100 | 15 | 25 |
Coordinates of different study sites along the Saudi Arabian coast of the Red Sea
| Location | Site No. | Latitude N | Longitude E | Remarks |
|---|---|---|---|---|
| Jazan | I | 16°25’6.85” | 42°45’49.08” | Fringing reef |
| II | 16°41’54.15” | 42°43’1.78” | Inland lagoon (dead mangrove) | |
| III | 16°43’54.71” | 42°42’29.12” | Inland lagoon (dead mangrove) | |
| IV | 16°47’3.69” | 42°40’23.07” | Fringing reef (near a sewage outlet) | |
| V | 17°3’3.16” | 42°27’8.85” | Fringing reef | |
| Al-Birk | VI | 17°48’0.89” | 41°53’21.16” | Inland lagoon (fish farm outlet) |
| VII | 17°57’9.17” | 41°41’10.91” | Fringing reef | |
| VIII | 18°7’11.42” | 41°34’52.77” | Fringing reef | |
| IX | 19°47’30.24” | 40°37’52.13” | Fringing reef | |
| Al-Lith | X | 20°9’56.94” | 40°12’50.01” | Inland lagoon (fish farm outlet) |
| Jeddah | XI | 21°16’8.74” | 39°7’34.40” | Fringing reef (sewage plant outlet) |
| XII | 21°58’57.73” | 38°58’44.60” | Inland lagoon | |
| XIII | 22°15’11.33” | 39°4’50.23” | Fringing reef | |
| Rabigh | XIV | 22°52’50.29” | 38°56’33.66” | Inland lagoon |
| XV | 22°51’3.09” | 38°57’35.99” | Inland lagoon | |
| XVI | 23°8’10.01” | 38°47’47.27” | Inland lagoon (fish farm outlet) | |
| XVII | 23°19’47.25” | 38°41’37.06” | Inland lagoon | |
| Al-Wajh | XVIII | 5°34’39.25” | 36°58’13.98” | Inland lagoon |
| XIX | 25°59’27.67” | 36°42’39.29” | Fringing reef | |
| Duba | XX | 27°25’52.30” | 35°36’9.54” | Inland lagoon |
Values of Pearson’s coefficient of correlation (r) indicating possible relationships between meiofaunal groups and different environmental parameters (Meio – total meiofauna; Nema – nematodes; Poly – polychaetes; Oligo – oligochaetes; Turb – turbellarians; Cope – copepods; Ostr – ostracods and Amph – amphipods)
| Parameter | Meio | Nema | Poly | Oligo | Turb | Cope | Ostr | Amph |
|---|---|---|---|---|---|---|---|---|
| Sand (%) | 0.675 Correlation is significant at the 0.01 level (2-tailed) | 0.591 Correlation is significant at the 0.01 level (2-tailed) | 0.39 | 0.29 | 0.34 | 0.614 Correlation is significant at the 0.01 level (2-tailed) | 0.24 | 0.06 |
| VC sand | −0.13 | −0.11 | 0.03 | −0.30 | 0.13 | −0.22 | −0.26 | 0.12 |
| CS sand | 0.32 | 0.24 | 0.26 | 0.00 | 0.39 | 0.37 | −0.10 | 0.10 |
| M sand | −0.08 | −0.08 | −0.08 | −0.09 | −0.10 | 0.06 | 0.07 | 0.01 |
| F sand | 0.38 | 0.34 | 0.09 | 0.40 | 0.13 | 0.38 | 0.492 Correlation is significant at the 0.05 level (2-tailed); | −0.17 |
| VF sand | −0.448 Correlation is significant at the 0.05 level (2-tailed); | −0.35 | −0.23 | −0.09 | −0.502 Correlation is significant at the 0.05 level (2-tailed); | −0.573 Correlation is significant at the 0.01 level (2-tailed) | −0.28 | 0.01 |
| Silt-clay | −0.675 Correlation is significant at the 0.01 level (2-tailed) | −0.591 Correlation is significant at the 0.01 level (2-tailed) | −0.39 | −0.29 | −0.34 | −0.614 Correlation is significant at the 0.01 level (2-tailed) | −0.24 | −0.06 |
| pH | 0.39 | 0.33 | 0.31 | 0.32 | 0.35 | 0.12 | 0.16 | 0.13 |
| EC | −0.28 | −0.29 | −0.11 | −0.06 | −0.01 | −0.25 | 0.02 | −0.03 |
| OC (%) | −0.38 | −0.39 | −0.19 | −0.19 | −0.01 | −0.23 | −0.13 | −0.11 |
| Temperature | 0.17 | 0.31 | −0.10 | −0.25 | −0.09 | 0.08 | 0.06 | −0.08 |
| Salinity | −0.02 | 0.03 | −0.13 | −0.11 | −0.21 | 0.10 | −0.02 | −0.02 |