Meiofauna of the Red Sea Mangroves with Emphasis on Their Response to Habitat Degradation: Sudan’s Mangroves as a Case Study

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Oceanographic and Biological Aspects of the Red Sea

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Abstract

This chapter provides an overview on the meiofauna of mangroves in the Red Sea coast of Sudan, with an emphasis on the meiofaunal response to mangrove degradation. Investigations of meiofaunal response were based on comparing sites subjected to human impacts resulting in complete clearance and partial clearance of mangrove cover with a non-cleared site with intact mangrove cover in the southern coast of the Sudanese Red Sea. At the degraded mangrove sites, sediment sorting, mean grain size, water and organic contents in sediments changed significantly, and the variation between shoreward (high-and mid-intertidal) and seaward (low-intertidal, shallow subtidal) zones intensified. These changes were attributed to modification of the sediment depositional and reworking processes at the deforested sites. Correlated significant changes in the structure of meiofauna at higher taxonomic levels were indicated by ANOSIM, resulting from the different responses of the various meiofaunal groups to the deforestation impact. Changes in the meiofaunal community structure at higher taxonomic levels were mainly due to increased copepod/nauplii and decreased nematode abundances at the deforested sites. Among other groups, abundances of Ostracoda, Acari and Kinorhyncha were also reduced, but some others, for example, Oligochaetes, Platyhelminthes, Gnathostomulida, Gastrotrichs, and Cnidaria became more frequent and abundant at the partially-deforested sites. Similar changes occurred at lower taxonomic levels in the nematode community structure. While changes in the abundance of different nematode species have contributed to the community variation at the deforested sites, the decrease in the abundance of Terschellingia sp. was the most important. The nematode species Shannon-Wiener diversity became significantly higher at the partially-deforested site and lower at the completely deforested site, in comparison with the natural non-cleared mangrove site. The increased richness and diversity at the partially-deforested site, which was also indicated by species k-dominance curves, were attributed to the habitat heterogeneity of the patchy mangrove vegetation. These observations were also considered in the context of Connell’s intermediate disturbance hypothesis “with peak meifauna diversity at intermediate level of disturbance”. On the other hand, the results also recorded increased variability in the meiofaunal and nematode communities within the deforested sites, which was considered indicative of community stress. Seasonal variations of meiofaunal communities were also exaggerated at the deforested sites, which could be attributed to the decline of their resilience to seasonal changes due to loss of mangroves from the habitat. Among the nematode species, the relative abundance of selective deposit feeders showed a noticeable response, decreasing sharply at the deforested sites. This was related to the decline in the availability of organic/microbial food resulting from mangrove degradation. Other feeding guilds, especially non-selective deposit feeders, displayed an opposite trend, increasing in relative abundance as their feeding strategy might prove to be more energetically favourable with the decline of organic detritus and microbial contents at the deforested sites. Thus, the functional properties of the community were modified at the deforested areas, although nematode diversity was enhanced at the partially-deforested site. The overall feature of the change at the deforested sites was a shifting of ecosystem properties with consequent changes in the meiofauna, which indicated decline in the efficiency of the ecosystem function as a nursery ground for marine organisms, which represents one of the vital services provided by the mangrove ecosystem.

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References

  • Alongi DM (1987a) Intertidal zonation and seasonality of meiobenthos in tropical mangrove estuaries. Mar Biol 95:447–458

    Article  Google Scholar 

  • Alongi DM (1987b) The influence of the mangrove-derived tannins on intertidal meiobenthos in tropical estuaries. Oecologia (Berl) 71:537–540

    Article  Google Scholar 

  • Alongi DM (1987c) Inter-estuary variation and intertidal zonation of free-living nematode communities in tropical mangrove systems. Mar Ecol Prog Ser 40:103–114

    Article  Google Scholar 

  • Alongi DM (1990) Community dynamics of free living nematodes in some tropical mangroves and sandflat habitats. Bull Mar Sci 46:358–373

    Google Scholar 

  • Alongi DM, Christoffersen P (1992) Benthic infauna and organism-sediment relations in a shallow, tropical coastal area: influence of out welled mangrove detritus and physical disturbance. Mar Ecol Prog Ser 81:229–245

    Article  Google Scholar 

  • Andrassy I (1959) Einige Nematoden aus dem Roten Meer. Ann Hist Nat Mus Nat Hungarici 51:247–257

    Google Scholar 

  • Austen MC, McEvoy AJ, Warwick RM (1994) The specificity of meiobenthic community responses to different pollutants: results from microcosm experiments. Mar Pollut Bull 28:557–563

    Article  Google Scholar 

  • Austen MC, Widdicombe S, Villano-Pitacco N (1998) Effects of biological disturbance on diversity and structure of meiobenthic nematode communities. Mar Ecol Prog Ser 174:233–246

    Article  Google Scholar 

  • Boggs S Jr (1987) Principles of sedimentology and stratigraphy. Merrill Publishing Co., Toronto

    Google Scholar 

  • Clarke KR, Warwick RM (1994) Change in marine communities: an approach to statistical analysis and interpretation. Natural Environment Research Council, Plymouth Marine Laboratory, Plymouth

    Google Scholar 

  • Connell JH (1978) Diversity in tropical rain forests and coral reefs. Science 199:1302–1310

    Article  Google Scholar 

  • Coull BC, Chandler T (1992) Pollution and meiofauna: field, laboratory and mesocosmstudies. Oceanogr Mar Biol A Rev 30:191–271

    Google Scholar 

  • Davis JH (1940) The ecological and geological role of mangroves in Florida. Publs Carnegie Inst 517:303–412

    Google Scholar 

  • Death RG, Winterbourn MJ (1995) Diversity patterns in stream benthic invertebrate communities: the influence of the habitat stability. Ecology 76:1446–1460

    Article  Google Scholar 

  • Decraemer W, Coomans A (1978) Scientific report on the Belgian expedition to The Great Barrier Reef in 1967: Nematodes XII. Ecological notes on the nematode fauna in and around mangroves on Lizard Island. Aust J Mar Freshwat Res 29:497–508

    Article  Google Scholar 

  • Dittmann S (1993) Impact of foraging soldiercrabs (Decapoda: Mictyridae) on meiofauna in a tropical tidal flat. Rev Biol Trop 41(3):627–637

    Google Scholar 

  • Dittmann S (1996) Effects of macrobenthic burrows on infaunal communities in tropical tidal flats. Mar Ecol Prog Ser 134:119–130

    Article  Google Scholar 

  • Dittmann S (2000) Zonation of benthic communities in a tropical tidal flat of north-east Australia. J Sea Res 43:33–51

    Article  Google Scholar 

  • Dye AH (1983) Composition and seasonal fluctuations of meiofauna in a Southern African mangrove estuary. Mar Biol 73:165–170

    Article  Google Scholar 

  • Dye AH, Lasiak TA (1986) Microbenthos, meiobenthos and fiddler crabs: trophic interactions in a tropical mangrove sediment. Mar Ecol Prog Ser 32:259–264

    Article  Google Scholar 

  • Dyer KR (1986) Coastal and estuarine sediment dynamics. John Wiley & Sons Ltd., New York

    Google Scholar 

  • El-Serehy HA, Al-Misned FA, Al-Rasheid KA (2016) Population fluctuation and vertical distribution of meiofauna in the Red Sea interstitial environment. Saudi J Biol Sci (2015) 22:459–465

    Article  Google Scholar 

  • Fenchel T (1969) The ecology of marine microbenthos IV. Structure and function of the benthic ecosystem, its physical factors and the microfauna communities with special reference to the ciliated Protozoa. Ophelia 6:1–182

    Article  Google Scholar 

  • Fishelson I (1971) Ecology and distribution of the benthic fauna in the shallow waters of the Red Sea. Mar Biol 10:113–133

    Article  Google Scholar 

  • Fondo EN, Martens EE (1998) Effects of mangrove deforestation on macrofaunal densities, Gazi Bay, Kenya. Mangrove Salt Marshes 2:75–83

    Article  Google Scholar 

  • Gee JM (1989) An ecological and economic review of meiofauna as food for fish. Zool J Linn Soc 96:243–261

    Article  Google Scholar 

  • Gerlach SA (1958) Freilebende nematoden von den korallenriffen des Roten Meeres. Kiel Meeresforsch 14:241–246

    Google Scholar 

  • Gerlach SA (1964) Freilebende nematoden aus dem Roten Meer. Kiel Meeresforsch 20(Sonderheft):18–34

    Google Scholar 

  • Gerlach SA (1967) Freilebende meeres-nematoden von den Sarso-Inseln (Rotes Meer). Sonderdruck aus “Meteor” Forschungsergebnisse, Reihe D, Heft 2, Gebrüder Borntraeger, Berlin

    Google Scholar 

  • Gerlach SA (1971) On the importance of marine meiofauna for benthos communities. Oecologia (Berl) 6:176–190

    Article  Google Scholar 

  • Gerlach SA, Riemann F (1973/1974) The checklist of aquatic nematodes. A catalogue of Nematoda Adenophorea excluding the Dorylaimida. Veröff Inst Meeresforsch Bremerhaven, Supplement 4, Part 1 (1973) and Part 2 (1974)

    Google Scholar 

  • Hanafy MH, Mohammed DA, Ahmed AI (2011) Seasonal distribution of the littoral interstitial meiofauna in the northern Red Sea. Egypt. Egypt J AquatBiol Fish 15(2):35–51

    Article  Google Scholar 

  • Heip C (1980) Meiobenthos as a tool in the assessment of marine environmental quality. Rapp P-V Reun Cons Int Explor Mer 179:182–187

    Google Scholar 

  • Heip C, Vincx M, Vranken G (1985) The ecology of marine nematodes. Oceanogr Mar Biol Ann Rev 23:399–489

    Google Scholar 

  • Heip C, Warwick RM, Carr MR, Herman PMJ, Huys R, Smol N, Van Holsbeke K (1988) Analysis of community attributes of the benthic meiofauna of Frierfjord/Langesundfjord. Mar Ecol Prog Ser 46:171–180

    Article  Google Scholar 

  • Herman PMJ, Heip C (1988) On the use of meiofauna in ecological monitoring: who needs taxonomy? Mar Pollut Bull 19:665–668

    Article  Google Scholar 

  • Higgins RP, Thiel H (eds) (1988) Introduction to the study of meiofauna. The Smithsonian Institute Press, Washington, DC

    Google Scholar 

  • Hodda M, Nicholas WL (1985) Meiofauna associated with mangroves in the Hunter River Estuary and Fullerton Cove, South-Eastern Australia. Aust J Mar Freshwater Res 36:41–50

    Article  Google Scholar 

  • Hodda M, Nicholas WL (1986) Temporal changes in littoral meiofauna from the Hunter River estuary. Aust J Mar Freshwater Res 37:729–741

    Article  Google Scholar 

  • Hoffman JA, Katz J, Bertness MD (1984) Fiddler crab deposit-feeding and meiofaunal abundance in salt marsh habitats. J Exp Mar BiolEcol 82:161–174

    Article  Google Scholar 

  • Hopper BE, Meyers SP (1967) Population studies on benthic nematodes within a tropical seagrass community. Mar Biol 1:85–96

    Article  Google Scholar 

  • Hopper BE, Fell JW, Cefalu RC (1973) Effect of temperature on life cycle of nematodes associated with the mangrove (Rhizophora mangle) detrital system. Mar Biol 23:293–296

    Article  Google Scholar 

  • Huston MA (1994) Biological diversity. Cambridge University Press, Cambridge

    Google Scholar 

  • Khalil ASM (1994) An Ecological study on fishes of the mangrove ecosystems of the Sudanese Red Sea. M.Sc. Thesis, Dept of Zoology, University of Khartoum, Sudan

    Google Scholar 

  • Khalil, ASM (2000) Response of meiofauna to mangrove degradation in a dry semi-desert coastal habitat of the Red Sea (Sudan). Dubai International Conference on Desertification: toward Better Management of Arid and Semi-Arid Lands in the Twenty-First Century, 12–16 February 2000, Zayed International Prize for the Environment, Dubai, UAE

    Google Scholar 

  • Khalil ASM (2001) Response of meiofauna to mangrove deforestation in arid coastal habitats of the Red Sea (Sudan) with emphasis on free-living marine nematodes. Ph.D. Thesis, Centre for Tropical Marine Ecology, Bremen, ZMT Contributions no. 13, 82 pp

    Google Scholar 

  • Khalil ASM (2003) Response of meiofauna to mangrove degradation in a dry semi-desert coastal habitat of the Red Sea (Sudan). In: Alsharhan AS, Fowler A, Goudie AS, Abdellatif EM, Wood WW (eds) Desertification in the third millennium. Taylor & Francis, pp 139–150

    Google Scholar 

  • Khalil ASM, Krupp F (1994) Fishes of the mangrove ecosystem. In: comparative Ecological Analysis of Biota and Habitats in Littoral and Shallow Sublittoral Waters of the Sudanese Red Sea. Report for the period of April 1991 to December 1993. Faculty of Marine Science and Fisheries, Port Sudan, and Forschungs institut Senckenberg, Frankfurt

    Google Scholar 

  • Khalil ASM (2015) Mangroves of the red sea. In: Rasul NMA, Stewart ICF (eds) The Red Sea: the formation, morphology, oceanography and environment of a young ocean basin. Springer Earth System Sciences, Berlin, Heidelberg, pp 585–597

    Google Scholar 

  • Krishnamurthy K, Sultan Ali MA, Jeyseelan MJP (1984) Structure and dynamics of the aquatic food web community with special reference to nematodes in mangrove ecosystems. In: Soepadmo E, Rao AN, MacIntosh DJ (eds) ProcAsian symposium on mangrove environment, research and management. University of Malaysia, Kuala Lumpur, pp 429–452

    Google Scholar 

  • Lee JJ, Tenore K, Tietjen JH, Mastropaolo C (1974) An experimental approach toward understanding the role of meiofauna in a detritus based food web. Bull Mar Biol LabWoods Hole 147:488–489

    Google Scholar 

  • Lorenzen S (1981) Entwurf eines phylogenetischen Systems der freilebenden Nematoden. Veröff Inst Meeresforsch Bremerhaven, Supplement 7. Kommissionsverlag Franz Leuwer, Bremen

    Google Scholar 

  • MacNae W (1968) A general account of the fauna and flora of the mangrove swamps and forests in the Indo-West-Pacific Region. Adv Mar Biol 6:73–270

    Article  Google Scholar 

  • Mastaller M (1996) Destruction of mangrove wetlands – causes and consequences. Nat Resour Develop 43(44):37–57

    Google Scholar 

  • Mastaller M (1997) Mangroves: the forgotten forest between land and sea. Tropical Press Sdn. Bhd., Kuala Lumpur, Malaysia

    Google Scholar 

  • Mclntyre AD (1968) Ecology of marine meiobenthos. Biol Rev 44:245–290

    Article  Google Scholar 

  • Moens T, Vincx M (1997) Observations on the feeding ecology of estuarine nematodes. J Mar BiolAssoc UK 77:211–227

    Article  Google Scholar 

  • Moore CG, Bett BJ (1989) The use of meiofauna in marine pollution impact assessment. Zool J Linn Soc 96:263–280

    Article  Google Scholar 

  • Mutua AK (2009) Response of Benthic Fauna to Mangrove Degradation and Restoration in Gazi Bay – Kenya. Ph.D. Thesis, School of Biological Sciences, University of Nairobi, Kenya

    Google Scholar 

  • Mutua AK, Muthumbi A, Ntiba MJ, VanreuselA (2013) Patterns of meiofaunal colonisation as an indicator of reforested Rhizophoramucronatamangrove recovery in Gazi Bay, Kenya. W Indian Ocean J Mar Sci 12(1):25–35

    Google Scholar 

  • Netto SA, Attrill MJ, Warwick RM (1999) Sublittoral meiofauna and macrofauna of Rocas Atoll (NE Brazil): indirect evidence of a topographically controlled front. Mar Ecol Prog Ser 179:175–186

    Article  Google Scholar 

  • Nicholas WL, Elek JA, Stewart AC, Marples TC (1991) The nematode fauna of a temperate Australian mangrove mudflat, its population density, diversity and distribution. Hydrobiologia 209:13–27

    Article  Google Scholar 

  • Olafsson E (1995) Meiobenthos in mangrove areas in eastern Africa with emphasis on assemblage structure of free-living marine nematodes. Hydrobiologia 312:47–57

    Article  Google Scholar 

  • Olafsson E, Moore CG (1990) Control of meiobenthic abundance by macroepifauna in a subtidal muddy habitat. Mar Ecol Prog Ser 65:241–249

    Article  Google Scholar 

  • Olafsson E, Elmgren R, Papakosta O (1993) Effects of the deposit feeding benthic bivalve Macomabalthica on meiobenthos. Oecologia 93:457–462

    Article  Google Scholar 

  • Parker RH (1975) The study of benthic communities. Elsevier, Amsterdam, p 279

    Google Scholar 

  • Platt HM, Warwick RM (1983) Free living marine nematodes. Part I. British Enoplids. In: Kermack DM, Barnes RSK (eds) Synopsis of the British Fauna (New Series) No. 28. Cambridge University Press

    Google Scholar 

  • Platt HM, Warwick RM (1988) Free living marine nematodes. Part II. British Chromadorids. In: Kermack DM, Barnes RSK (eds) Synopsis of the British Fauna (New Series) No. 38. E. J. Brill / Dr. W. Backhuys, New York

    Google Scholar 

  • Pusceddu A, Gambi C, Corinaldesi C, Scopa M, Danovaro R (2014) Relationships between Meiofaunal Biodiversity and Prokaryotic Heterotrophic Production in Different Tropical Habitats and Oceanic Regions. PLoS ONE 9(3):e91056. https://doi.org/10.1371/journal.pone.0091056

    Article  Google Scholar 

  • Raffaelli D (1987) The behaviour of the Nematode/Copepod ratio in organic pollution studies. Mar Environ Res 23:135–152

    Article  Google Scholar 

  • Raffaelli D, Mason CF (1981) Pollution monitoring with meiofauna, using the ratio of nematodes to copepods. Mar Pollut Bull 12:158–163

    Article  Google Scholar 

  • Sabeel RAO, Vanreusel A (2015) Potential impact of mangrove clearance on biomass and biomass size spectra of nematode along the Sudanese Red Sea coast. Marine Environ Res 103:46–55

    Article  Google Scholar 

  • Saenger P, Sankare Y, Perry T (1996) Effects of pollution and over-cutting on mangroves. GEF Large Marine Ecosystem Project for the Gulf of Guinea. UNDP Report

    Google Scholar 

  • Sasekumar A (1993) Asian-Australian marine science projects: living coastal resources. In: Proceedings workshop on mangrove fisheries and connection. Australian International Development Assistance Bureau (AIDAB), Brisbane

    Google Scholar 

  • Sasekumar A (1994) Meiofauna of a mangrove shore on the west coast of peninsular Malaysia. Raffles Bull Zool 42:241–252

    Google Scholar 

  • Schratzberger M, Warwick RM (1998) Effects of physical disturbance on nematode communities in sand and mud: a microcosm experiment. Mar Biol 130:643–650

    Article  Google Scholar 

  • Schrijvers J, Okondo J, Steyaert M, Vincx M (1995) Influence of epibenthos on meiobenthos of the Ceriopstagal mangrove sediment at Gazi Bay, Kenya. Mar Ecol Prog Ser 128:247–259

    Article  Google Scholar 

  • Schrijvers J, Schallier R, Silence J, Okondo JP, Vincx M (1997) Interactions between epibenthos and meiobenthos in a high intertidal Avicennia marina mangrove forest. Mangr Salt Marsh 1:137–154

    Article  Google Scholar 

  • Snelgrove PR, Butman CA (1994) Animal-sediment relationship revisited: cause versus effect. Oceanogr Mar Biol Ann Rev 32:111–117

    Google Scholar 

  • Somerfield PJ, Gee JM, Aryuthaka C (1998) Meiofaunal communities in a Malaysian mangrove forest. J Mar BiolAssoc UK 78:717–732

    Article  Google Scholar 

  • Thiel H (1979) First quantitative data on Red Sea deep benthos. Mar Ecol Prog Ser 1:347–350

    Article  Google Scholar 

  • Tietjen JH (1969) The ecology of shallow water meiofauna in two New England estuaries. Oecologia (Berl) 2:251–291

    Article  Google Scholar 

  • Vanhove S, Vinx M, Van Gansbecke D, Gijselinck W, Schram D (1992) The meiobenthos of five mangrove vegetation types in Gazi Bay, Kenya. Hydrobiologia 247:99–108

    Article  Google Scholar 

  • Warwick RM (1988a) Effects on community structure of a pollution gradient: a summary. Mar Ecol Prog Ser 46:207–211

    Article  Google Scholar 

  • Warwick RM (1988b) The level of taxonomic discrimination required to detect pollution effects. Mar Pollut Bull 19:259–268

    Article  Google Scholar 

  • Warwick RM, Clarke KR (1993) Increased variability as a symptom of stress in marine communities. J ExpMar BiolEcol 172:215–226

    Google Scholar 

  • Warwick RM, Carr MR, Clarke KR, Gee JM, Green RH (1988) A mesocosm experiment on the effects of hydrocarbon and copper pollution on a sublittoral soft-sediment meiobenthic community. Mar Ecol Prog Ser 46:181–191

    Article  Google Scholar 

  • Warwick RM, Platt HM, Somerfield PJ (1998) Free Living Marine Nematodes. Part III. British Monhysterids. In: Barnes RSK, Crothers JH (eds) Synopsis of the British Fauna (New Series) No. 53. Field Studies Council, Shrewsbury, UK

    Google Scholar 

  • Wieser W (1953) Die beziehung zwischen mundhöhlengestalt, ernahrungsweise und vorkommen bei freilebenden marinen nematoden. Ark Zool 4:439–483

    Google Scholar 

  • Wieser W (1959) Free-living nematodes-IV. General part. Acta Univ Lund N F Adv 55:1–111

    Google Scholar 

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Khalil, A.S.M. (2019). Meiofauna of the Red Sea Mangroves with Emphasis on Their Response to Habitat Degradation: Sudan’s Mangroves as a Case Study. In: Rasul, N., Stewart, I. (eds) Oceanographic and Biological Aspects of the Red Sea. Springer Oceanography. Springer, Cham. https://doi.org/10.1007/978-3-319-99417-8_23

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