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Benthic ostracods (crustacean) as a nearshore pollution bio-monitor: examples from the Red Sea Coast of Egypt

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Abstract

Benthic ostracods are deemed as one of the most useful micro-fauna for biomonitoring in shallow marine ecosystem, which are sensitive to environmental changes that can be reflected by their diversity and abundances. The pollution leads to high dominance index and low abundance ostracod communities. Therefore, eighteen sediment samples were collected from Ras Gharib and Quseir sites, along the Red Sea coast, to assess the ostracods response toward the anthropogenic environmental disturbances. Jugosocythereis borchersi, Alocopocythere reticulata, and Loxocorniculum ghardaqensis are the most abundant ostracods in the study localities. To evaluate the linkage between ostracods and contaminated sediments, metal concentrations in the sediments were measured using inductively coupled plasma optical-emission spectrometry (ICP-OES). We observed a significant spatial difference in elemental distribution in sediment samples, and some elements are of higher contributions than the average marine sediment composition. The quantitative analysis of benthic ostracod associations was processed statistically with geochemical data and differentiated the study area into two environments, based on the degrees of contamination. Quseir is encompassing the most contaminated stations. It is characterized by sediments richer in heavy metals, higher silt, and higher organic matter contents. Contaminated environments favor the presence of pollution-tolerant species (e.g., J. borchersi, C. torosa, L. ghardaqensis, G. triebeli, M. striata, A. reticulata, and partly, C. dimorpha). Conversely, Ras Gharib is less polluted with metals and organic matter, and is characterized by pollution-sensitive species (X. rhomboidea). Noteworthy, a low density of ostracods was observed at the expense of the diversity around contaminated stations of the Quseir site.

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Data availability

The datasets used and/or analyzed during the current study are included in the published article and its supplementary information files and are available from the corresponding author on reasonable request.

Change history

Abbreviations

J. borchersi :

Jugosocythereis borchersi

H. rubrimaris :

Hiltermannicythere rubrimaris

L .ghard :

Loxocorniculum ghardaqensis

M. striata :

Moosella striata

G. triebeli :

Ghardaglaia triebeli

X. rhomboidea :

Xestolebris rhomboidea

X. ghardaqae :

Xestoleberis ghardaqae

C. dimorpha :

Cytheroma dimorpha

C. torosa :

Cyprideis torosa

A. reticulata :

Alocopocythere reticulata.

References

  • Alin S, Cohen AS, Bills R, Mukwaya M, Michel M, Tiercelin K, Coveliers P, Keita S, West K, Soreghan M, Kimbadi S, Ntakimazi G (1999) Effects of landscape disturbance on animal communities in Lake Tanganika, East Africa. Conserv Biol 13:1017–1033

    Google Scholar 

  • Anadon, P., Gliozzi, E., Mazini, I., 2002. Paleoenvironmental reconstruction of marginal marine environments from combined paleoecological and geochemical analysis on ostracods. In: Holmes, J.A., Chivas, A.R. (Eds.), the Ostracoda: Applications in Quaternary Research, Geophysical Monograph, 131. American Geophysical-Union, Washington, DC, pp. 227–247

  • Badr NBE, El-Fiky AA, Mostafa AR, Al-Mur BA (2009) Metal pollution records in core sediments of some Red Sea coastal areas, Kingdom of Saudi Arabia. Environmental Monitoring Assessment 155:509–526

    CAS  Google Scholar 

  • Bergin F, Kucuksezgin F, Uluturhan E, Barut IF, Meric E, Avsar N, Nazik A (2006) The response of benthic foraminifera and ostracod to heavy metal pollution in Gulf of Izmir. Estuary, Coast. Shelf Science 66:368–386

    CAS  Google Scholar 

  • Bodergat, A.M., Ikeya, N., 1988. Distribution of recent Ostracod in Ise and Mikawa Bays, Pacific coast of central Japan. In: Hanai, T., Ikeya, N., Ishizaki, K. (Eds.), Evolutionary biology of Ostracod- its fundamentals and applications. Kodansha, Tokyo, Elsevier, Amsterdam, pp. 413–428

  • Bonaduce, G., Ciliberto, B., Minichelli, G., Masoli, M., Pugliese, N., 1983. The Red Sea benthic ostracods and their geographical distribution. Proceedings of the 8th International Symposium on Ostracoda: Applications of Ostracoda, (R. F. Maddocks, Ed.) Univ. Houston Geoscience: 472–491

  • Boomer I, Eisenhauer G (2002) Ostracod faunas as palaeoenvironmental indicators in marginal marine environments. In: Holmes JA, Chivas AR (eds) The Ostracoda: applications in quaternary research, geophysical monograph, vol. 131. American Geophysical Union, Washington, DC, pp 135–149

    Google Scholar 

  • Callender, E., 2005. Heavy metals in the environment-historical trends. In: Lollar, B. S. (Ed), Holland, H.D., Turekian, K.K. (Ex. Eds), Environmental Geochemistry. Treatise on Geochemistry, vol. 9, 612 p., Elsevier, Amsterdam

  • Carman KR, Fleeger JW, Pomarico SM (2000) Does historical exposure to hydrocarbon contamination alter the response of benthic communities to diesel contamination? Mar. Environ Res 49:255–278

    CAS  Google Scholar 

  • Chivas AR, De Deckker P, Shelley JMG (1986) Magnesium and strontium in nonmarine ostracods shells as indicators of paleosalinity and paleotemperature. Hydrobiologia 143:135–142

    CAS  Google Scholar 

  • Dean WE (1974) Determination of carbonate and organic matter in calcareous sediments and sedimentary rocks by loss in ignition: comparison with other methods. J Sediment Petrol 44:242–248

    CAS  Google Scholar 

  • Diaz RJ, Rosenberg R (1995) Marine benthic hypoxia: a review of its ecological effects and the behavioral responses of benthic macrofauna. Oceanography Marine Biology Annual Review 33:245–303

    Google Scholar 

  • Duchart P, Calvert S, Price N (1973) Distribution of trace metals in the pore waters of shallow marine sediments. Limnology and Oceanography 18:605–610

    CAS  Google Scholar 

  • Eager SH (1999) Distribution of Ostracoda around a coastal sewer outfall: a case study from Wellington, New Zealand. Journal of Royal Society New Zealand 29:257–264

    Google Scholar 

  • El-Kahawy R, El-Shafeiy M, Helal SA, Aboul-Ela N, El-Wahab MA (2018) Morphological deformities of benthic foraminifera in response to nearshore pollution of the Red Sea, Egypt. Environmental Monitoring and Assessment 190:312. https://doi.org/10.1007/s10661-018-6695-2

    Article  CAS  Google Scholar 

  • El-Komi, M. M., Emara A.M. and Mona, M.H., 2002. Hydrographical conditions and benthic assemblages in the Suez Gulf. Pakistan Journal of Marine Sciences, Vol. 11(1&2), 1–18, 2002

  • Elshanawany, R., 2010. Microfossil assemblages as proxies to reconstruct anthropogenic induced eutrophication of two marginal Eastern Mediterranean Basins. PhD thesis, University of Bremen, Germany

  • El-Sorogy, A.S., Abd El-Wahab, M., Nour, H.E., Ziko, A., Shehata, W., 2006. Faunal assemblages and sedimnet chemistryof some lagoons along the Red Sea coast, Egypt.Egypt. J. Paleontol. (6):193–224

  • El-Taher A, Madkour HA (2014) Environmental and radioecologicalstudies on shallowmarine sediments from harbourareas along the Red Sea coast of Egypt for identification ofanthropogenic impacts. Isotopes in Environmental andHealth Studies 50(1):120–133

    CAS  Google Scholar 

  • Folk RL, Ward WC (1957) Brazos River bar: a study in the significance of grain size parameters. J Sediment Res 27(1):3–26

    Google Scholar 

  • Frenzel P, Boomer I (2005) The use of ostracods from marginal marine, brackish waters as bioindicators of modern and quaternary environmental change. Palaeogeography., Palaeoclimatology, Palaeoecology 225:68–92

    Google Scholar 

  • Gabrié C, Montaggioni L (1982) Sedimentary facies from the modern coral reefs, Jordan gulf of Aqaba a, Red Sea. Coral Reefs 1(2):115–124

    Google Scholar 

  • Gross MG (1971) Carbon determination. In: Carver RE (ed) Procedures in sedimentary petrology. John Wiley and Sons, New York, pp 573–596

    Google Scholar 

  • Hammer Ø, Harper DAT, Ryan PD (2009) PAST- Palaeontological Statistics. In: version 1, vol 89. University of Oslo, Oslo, pp 1–31

    Google Scholar 

  • Hartmann G (1964) Neontological and paleontological classification of Ostracoda. Ostracods as ecological and palaeoecological indicators. Pubbl Stn Zool Napoli 33:550–587

    Google Scholar 

  • Hegazy MN, Effat HA (2010) Monitoring some environmental impacts of oil industry on coastal zone using different remotely sensed data. Egypt J Remote Sens Space Sci 13(1):63–74

    Google Scholar 

  • Helal S, Abd El-Wahab M (2004) Recent Ostracods from marine sediments of Safaga Bay, Red Sea, Egypt. Egypt Jour Paleontology 4:75–93

    Google Scholar 

  • Helal, S., Abd El-Wahab, M., 2010. Zoogeography and taxonomy of the recent marine ostracod in the Egyptian Red Sea mangrove protected areas. Fifth international conference on the Geology of the Tethys Realm, South Valey. UNI: 55–70

  • Helal S, Abd El-Wahab M (2012) Distribution of podocopid ostracods in mangrove ecosystems along the Egyptian Red Sea coast. Crustaceana 85(14):1669–1696

    Google Scholar 

  • Irizuki T, Takimoto A, Sako M, Nomura R, Kakuno K, Wanishi A, Kawano S (2011) The influences of various anthropogenic sources of deterioration on meiobenthos (Ostracod) over the last 100 years in Suo-Nada in the Seto Inland Sea, southwest. Japanese Marine Pollution Bulletin 62:2030–2041

    CAS  Google Scholar 

  • Irizuki T, Ito H, Sako M, Yoshioka K, Kawano S, Nomura R, Tanaka Y (2015) Anthropogenic impacts on meiobenthic Ostracod (Crustacea) in the moderately polluted Kasado Bay, Seto Inland Sea, Japan, over the past 70 years. Mar Pollut Bull 91(1):149–159

    CAS  Google Scholar 

  • Kemp J, Radke CL, Olley J, Juggins S, Deckker P (2012) Holocene lake salinity changes in the Wimmera, southeastern Australia, provide evidence for millennial-scale climate variability. Quat Res 77:65–76

    CAS  Google Scholar 

  • Lee MR, Correa JA (2005) Effects of copper mine tailings disposal on littoral meiofaunal assemblages in the Atacama region of northern Chile. Mar Environ Res 59:1–18

    CAS  Google Scholar 

  • Lenihan HS, Peterson CH, Kim SL, Conlan KE, Fairey R, McDonald C, Grabowski JH, Oliver JS (2003) Variation in marine benthic community composition allows discrimination of multiple stressors. Mar Ecol Prog Ser 261:63–73

    Google Scholar 

  • Leps J, Smilauer P (2003) Multivariate analysis of ecological data using CANOCO. Cambridge University Press, New York 283 pp

    Google Scholar 

  • Li Y-H (2000) A compendium of geochemistry: from solar nebula to the human brain. Princeton University Press, Princeton 475 pp

    Google Scholar 

  • Lili F, Irizuki T, Sampei Y (2013) Spatial distribution of recent ostracod assemblages and depositional environments in Jakarta Bay, Indonesia, with relation to environmental factors. Paleontology Research 16:267–281

    Google Scholar 

  • Liljenstroem, S., Widbom, B., Mattson, J., 1987. Effects of two oil refinery effluents on benthic Meiofauna in Mesocosms. Swedish Environmental Research Institute. 38 pp.

  • Lim RP, Wong MC (1986) The effects of pesticides on the population dynamics and production of Stenocypris major Baird (Ostracoda) in rice fields. Archive Hydrobiology 106:421–427

    CAS  Google Scholar 

  • Long ER, MacDonald DD, Smith SL, Calder FD (1995) Incidence of adverse biological effects within ranges of chemical concentrations in marine and estuarine sediments. Environ Manag 19(1):81–97

    Google Scholar 

  • Maddocks, R. F. 1985. One hundred million years of predation on Ostracods: the fossil record in Texas. In Hanai, T, lkeya, N, lshizaki, K.(eds.).1988. evolutionary biology of ostracoda its fundamentals and applications. Proceedings of the Ninth International Symposium on Ostracoda, held in Shizuoka, Japan, 29 July-2 August 1985, KODANSHA, Tokyo & ELSEVIER Amsterdam oxford- New York-Tokyo.1988: 637–685

  • Mansour A (1995) Sedimentary facies and carbonate-siliciclastic transition of Sharm El Bahari and Sharm El Qibli, Red Sea, Egypt. Egypt J Geol 39(1):57–76

    Google Scholar 

  • Mansour, A. M., Nawar, A. H. and Mohamed, A. W., 2000. Geochemistry of coastal marine sediments and their contaminant metals, Red Sea, Egypt: a legacy for the future and a tracer to modern sediment dynamics. Sedimen. of Egypt,8: 231–242

  • Mansour AM, Nawar AH, Madkour HA (2011) Metal pollution in marine sediments of selected harbours andindustrial areas along the Red Sea coast of Egypt. Ann. Naturhist. Mus. Wien, Serie A 113:225–244

    Google Scholar 

  • Mazzola A, Mirto S, Danovaro R (1999) Initial fish-farm impact on meiofaunal assemblages in coastal sediments of western Mediterranean. Mar Pollut Bull 38:1126–1133

    CAS  Google Scholar 

  • Mette W, Roozbahani P (2012) Late Permian (Changsingian) ostracods of the Bellerophon Formation at Seis (Siusi) (Dolomites, Italy). J Micropalaeontol 31:73–87

    Google Scholar 

  • Millward RN, Carman KR, Fleeger JW, Gambrell RP, Portier R (2004) Mixtures of metals and hydrocarbon elicit complex responses by a benthic invertebrate community. J Exp Mar Biol Ecol 310:115–130

    CAS  Google Scholar 

  • Mirto S, La Rosa T, Danovaro R, Mazzola A (2000) Microbial and meiofaunal response to intensive mussel-farm biodeposition in coastal sediments of the western Mediterranean. Mar Pollut Bull 40:244–252

    CAS  Google Scholar 

  • Mohammed M, Al-Wosabi M, Keyser D, Al-Kadasi WM (2012) Distribution and taxonomy of shallow marine Ostracods from northern Socotra Island (Indian Ocean)-Yemen. Rev Micropaleontol 55(4):149–170

    Google Scholar 

  • Moore, R. C., 1961. Treatise on invertebrate paleontology, part Arthropoda, (Ostracod). Geological Society American University Kansas Press, 422 pp

  • Moore C, Harries D, Ware F (1997) The impact of the SeaEmpress oil spill on the sandy shore meiofauna of south west Wales. CCW Sea Empress Contract Report 230

  • Morcos SA (1970) Physical and chemical oceanography of the Red Sea. Oceanogr Mar Biol Ann Rev 8(73):202

    Google Scholar 

  • Nour HE, Nouh E (2020) Comprehensive pollution monitoring of the Egyptian Red Sea coast by using the environmental indicators. Environ Sci Pollut Res 27:28813–28828

    CAS  Google Scholar 

  • Orive, E., Elliott, M., de Jorge, V.V., 2002. Nutrients and eutrophication in estuaries and coastal waters, developments in hydrobiology 164. Kluwer Academic Publishers

  • Piller WE, Pervesler P (1989) The Northern Bay of Safaga (Red Sea, Egypt): an actuopaleontological approchs. I: topography and bottom. Facies.Beitr.Palantologie, Osterr 15:103–147

    Google Scholar 

  • Pint A, Frenzel P (2017) Ostracod fauna associated with Cyprideis torosa–an overview. Journal of Micropalaeontology 36(1):113–119

    Google Scholar 

  • Poquet JM, Mezquita F, Rueda J, Miracle AR (2008) Loss of Ostracod biodiversity in Western Mediterranean wetlands. Aquatic Conservation Marine and Freshwater Ecosystem 18:280–296

    Google Scholar 

  • Rasul, N., Stewart, I,. Nawab, Z., 2015. Introduction to the Red Sea; its origin, structure, and environment. The Red Sea, 1–28

  • Ruiz, F., 1994. Los ostracodos del litoral de la provincia de Huelva. PhD thesis, Huelva University, 275 pp.

  • Ruiz F, Gonzalez-Regalado ML, Borrego J, Morales JA (1997) The response of ostracod assemblages to recent pollution and sedimentary processes in the Huelva estuary, SW Spain. Sci Total Environ 207:91–103

    Google Scholar 

  • Ruiz F, Gonzalez-Regalado ML, Baceta JI, Muoz JM (2000) Comparative ecological analysis of the ostracod faunas from low- and high-polluted southwestern Spanish estuaries: a multivariate approach. Mar Micropaleontol 40:345–376

    Google Scholar 

  • Ruiz F, Gonzlez-Regalado ML, Borrego J, Abad M, Pendón JG (2004) Ostracoda and foraminifera as short-term tracers of environmental changes in very polluted areas: the Odiel Estuary (SW Spain). Environ Pollution 129:49–61

    CAS  Google Scholar 

  • Ruiz F, Abad M, Bodergat AM, Carbonel P, Rodríguez-Lázaro J, González-Regalado ML, Toscano A, García EX, Prenda J (2013) Freshwater ostracods as environmental tracers. International Journal Environmental Science Technology 10:1115–1128

    CAS  Google Scholar 

  • Samir AM (2000) The response of benthic foraminifera and ostracods to various pollution sources: a study from two lagoons in Egypt. J Foraminifer Res 30(2):83–98

    Google Scholar 

  • Shannon, C. E., and Weaver, W., 1948. A mathematical theory of communication. Bell Syst. Tech. J. (27): 379–423 and 623–656

  • Steichen DJ, Holbrook SJ, Osenberg CW (1996) Distribution and abundance of benthic and demersal macrofauna within a natural hydrocarbon seep. Mar. Ecol. Prog Ser 138:71–82

    Google Scholar 

  • Suguio K (1973) Introdução à Sedimentologia. Edgard Blucher, São Paulo 317p

    Google Scholar 

  • USGS. 1995 Available from: http://minerals.cr.usgs.gov/geo_chem_stand/marine.html

  • Van der Merwe, C., 2003. The assessment of the influence of treated underground mine water on the benthic fauna in a portion of the Blesbokspruit Ramsar Site. Mini-thesis for Magister Artium in Environmental Management. Rand Afrikaans University, South Africa

  • Watzin MC, Roscigno PR (1997) The effects of zinc contamination on the recruitment and early survival of benthic invertebrates in an estuary. Mar Pollut Bull 34:443–455

    CAS  Google Scholar 

  • Yasuhara M, Yamazaki H, Irizuki T, Yoshikawa S (2003) Temporal changes of ostracode assemblages and anthropogenic pollution during the last 100 years, in sediment cores from Hiroshima bay, Japan. Holocene 13:527–536

    Google Scholar 

  • Yasuhara M, Hunt G, Breitburg D, Tsujimoto A, Katsuki K (2012) Human induced marine ecological degradation: micropaleontological perspectives. Ecology and Evolution 2:3242–3268

    Google Scholar 

  • Youssef M, Madkour H, Mansour A, Alharbi W, El-Taher A (2017) Invertebrate shells (mollusca, foraminifera) as pollution indicators, Red Sea Coast, Egypt. J Afr Earth Sci 133:74–85

    CAS  Google Scholar 

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Acknowledgments

The authors express their gratitude to the Cairo University for funding the chemical analyses. We are grateful to the editor Dr. Sarma VVSS and the two anonymous reviewers for considering the manuscript and help evolving it.

Funding

Partial financial support was received from Cairo University for the geochemical analysis.

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Nabil Aboul-Ela, Sobhi Helal, and M. Abd El-Wahab proposed and designed the research study. Ramadan El-Kahawy contributed to the acquisition of data. R. El-Kahawy, M. El-Shafeiy, and Sobhi Helal analyzed the data and wrote the manuscript. All authors approved the final version of the manuscript.

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Correspondence to Moataz El-Shafeiy.

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The original online version of this article was revised: The image of Figure 9, citations of Figures 7, 8, 9 and 10 and the captions of Figures 9 and 10 are modified in this paper.

Supplementary information

ESM 1

Species distribution chart showing the ostracods density at the two studied sites. (PNG 1806 kb)

High resolution (TIF 363 kb)

ESM 2

Percentage of all species, genera, and families collected from the two sampling sites (Ras Gharib and Quseir). (PNG 1908 kb)

High resolution (TIF 238 kb)

ESM 3

1–3: Jugosocythereis borchersi (Hartmann 1964), Sample no. Q.2; 4: Paranesidean. sp2. Bonaduce, Ciliberto, Minichelli, Masoli & Pugliese, 1983, Sample no. Q.5; 5–6: Paranesidea fracticorallicola Maddocks, 1969, Sample no. Q.2; 7–8: Neonesidea schulzi (Hartmann 1964), Sample no. Q.6; 9: Triebelina sertata Triebel, 1948, Sample no. G.8; 10: Cytherelloidea n. sp1. Bonaduce, Ciliberto, Minichelli, Masoli & Pugliese1983, Sample no. Q.3; 11: Hiltermannicythere rubrimaris (Hartmann 1964), Sample no. Q.7; 12-Moosella striata Hartmann 1964, Sample no. G.8; 13: Caudites levis Hartmann 1964, Sample no. Q.9; 14: Alocopocythere reticulata (Hartmann 1964), Sample no. Q.1; 15: Cyprideis torosa, (Jones, 1850), Sample no. Q.2 (PNG 1.05 mb)

High resolution (TIF 3.39 mb)

ESM 4

1: Bishopina cf. spinulosa (Brady, 1868), Sample no. Q.3; 2: Loxoconcha gurneyi Bate & Gurney, 1981, Sample no. G.9; 3: Loxocorniculum ghardaqensis (Hartmann 1964), Sample no. Q.2; 4- Sclerochilus rectomarginatus Hartmann 1964, Sample no. Q.6; 5: Hemicytherura videns (Müller, 1894), Sample no. Q.5; 6: Chartocythere arenicola (Hartmann 1964), Sample no. G.8; 7: Ghardaglaia triebeli Hartmann 1964, Sample no. Q.2; 8: Cytheroma dimorpha Hartmann 1964, Sample no. Q.7; 9: Paradoxostoma breve Müller, 1894, Sample no. Q.6; 10: Paradoxostoma parabreve Hartmann 1964, Sample no. Q.9; 11: Xestoleberis ghardaqae. Hartmann 1964, Sample no. Q.2; 12: Xestoleberis rhomboidea Hartmann 1964, Sample no. Q.3 (PNG 802 kb)

High resolution (TIF 2.55 mb)

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El-Kahawy, R., El-Shafeiy, M., Helal, S. et al. Benthic ostracods (crustacean) as a nearshore pollution bio-monitor: examples from the Red Sea Coast of Egypt. Environ Sci Pollut Res 28, 31975–31993 (2021). https://doi.org/10.1007/s11356-020-12266-x

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