Abstract
This paper aims to contribute to the use of mangrove cupped oyster, Crassostrea rhizophorae, as a biomonitor species for chemical contamination assessment in mangrove-lined Caribbean coastal systems. Sampling was carried out in eight localities (three in Nicaragua and five in Colombia) with different types and levels of contamination. Oysters were collected during the rainy and dry seasons of 2012–2013 and the tissue concentrations of metals, polycyclic aromatic hydrocarbons (PAHs), and persistent organic pollutants (POPs) were determined. Low tissue concentrations of metals (except Hg) and PAHs; moderate-to-high tissue concentrations of Hg, hexachlorocyclohexanes (HCHs), and dichlorodiphenyl-trichloroethanes (DDTs); detectable levels of chlorpyrifos, polychlorinated biphenyls (PCBs) (mainly CB28, CB118, CB138 and CB 153) and brominated diphenyl ethers 85 (BDE85); and negligible levels of musks were recorded in Nicaraguan oysters. A distinct profile of POPs was identified in Colombia, where the tissue concentrations of PCBs and synthetic musk fragrances were low to moderate, and Ag, As, Cd, Pb, and PAHs ranged from moderate to extremely high. Overall, the values recorded for HCHs, DDTs and PCBs in Nicaraguan mangrove cupped oysters greatly exceeded the reference values in tissues of C. rhizophorae from the Wider Caribbean Region, whereas only the levels of PCBs were occasionally surpassed in Colombia. Different contaminant profiles were distinguished between oysters from Nicaragua and Colombia in radar plots constructed using the main groups of contaminants (metals, PAHs, musks, PCBs, and organochlorine pesticides (OCPs)). Likewise, integrated pollution indices revealed differences in the levels of contaminants. Moreover, the profiles and levels in oyster tissues also varied with season. Thus, principal component analysis clearly discriminated Nicaraguan and Colombian localities and, especially in Colombia, seasonal trends in chemical contamination and differences amongst localities were evidenced. The geographical and environmental disparity of the studied scenarios may represent to a large extent the diversity of mangrove-lined Caribbean coastal systems and therefore the present results support the use of C. rhizophorae as suitable biomonitor species at Caribbean regional scale, where seasonal variability is a major factor controlling pollutant mobility and bioavailability.
Similar content being viewed by others
References
Aguirre-Rubi JR, Luna-Acosta A, Ortiz-Zarragoitia M, Zaldibar B, Izagirre U, Villamil L, Marigómez I (submitted) Assessment of ecosystem health disturbance in mangrove-lined Caribbean coastal systems using the oyster Crassostrea rhizophorae as sentinel species.
Alfonso JA, Handt H, Mora A, Vásquez Y, Azocar J, Marcano E (2013) Temporal distribution of heavy metal concentrations in oysters Crassostrea rhizophorae from the central Venezuelan coast. Mar Pollut Bull 73:394–398
Alonso DL, Latorre S, Castillo E, Brandão PFB (2013) Environmental occurrence of arsenic in Colombia: a review. Environ Pollut 186:272–281
Amado-Filho GM, Salgado LT, Rebelo MF, Rezende CE, Karez CS, Pfeiffer WC (2008) Heavy metals in benthic organisms from Todos os Santos Bay, Brazil. Brazilian J Biol 68:95–100
Angulo E (1996) The Tomlinson Pollution Load Index applied to heavy metal, ‘Mussel-Watch’ data: a useful index to assess coastal pollution. Sci Total Environ 187:19–56
Bartolomé L, Etxebarria N, Martínez-Arkarazo I, Raposo JC, Usobiaga A, Zuloaga O (2010) Distribution of organic microcontaminants, butyltins, and metals in mussels from the Estuary of Bilbao. Arch Environ Contam Toxicol 59:244–254
Basu N, Scheuhammer AM, Bursian SJ, Elliott J, Rouvinen-Watt K, Chan HM (2007) Mink as a sentinel species in environmental health. Environ Res 103:130–144
Baumard P, Budzinski H, Michon Q, Garrigues P, Burgeot T, Bellocq J (1998) Origin and bioavailability of PAHs in the Mediterranean sea from mussel and sediment records. Estuar Coast Shelf Sci 47:77–90
Bayen S (2012) Occurrence, bioavailability and toxic effects of trace metals and organic contaminants in mangrove ecosystems: a review. Environ Int 48:84–101
Beeby A (2001) What do sentinels stand for? Environ Pollut 112:285–298.
Beiras R, Durán I, Parra S, Urrutia MB, Besada V, Bellas J, Viñas L, Sánchez-Marín P, González-Quijano A, Franco MA, Nieto O, González JJ (2012) Linking chemical contamination to biological effects in coastal pollution monitoring. Ecotoxicology 21:9–17
Bellas J, Nieto O, Beiras R (2011) Integrative assessment of coastal pollution: development and evaluation of sediment quality criteria from chemical contamination and ecotoxicological data. Cont Shelf Res 31:448–456
Bellas J, Albentosa M, Vidal-Liñán L, Besada V, Franco MA, Fumega J, González-Quijano A, Viñas L, Beiras R (2014) Combined use of chemical, biochemical and physiological variables in mussels for the assessment of marine pollution along the N-NW Spanish coast. Mar Environ Res 96:105–117
Bodin N, N’Gom Ka R, Le Loc’h F, Raffray J, Budzinski H, Peluhet L, de Morais LT (2011) Are exploited mangrove molluscs exposed to persistent organic pollutant contamination in Senegal, West Africa? Chemosphere 84:318–327
Bosire JO, Dahdouh-Guebas F, Walton M, Crona BI, Lewis RR, Field C, Kairo JG, Koedam N (2008) Functionality of restored mangroves: a review. Aquat Bot 89:251–259
Campos NH (1990) La contaminación por metales pesados en la Ciénaga Grande de Santa Marta, Caribe Colombiano. Caldasia 16:231–243
Carvalho FP, Villeneuve JP, Cattini C, Rendón J, de Oliveira JM (2009a) Pesticide and PCB residues in the aquatic ecosystems of Laguna de Terminos, a protected area of the coast of Campeche, Mexico. Chemosphere 74:988–995
Carvalho FP, Villeneuve JP, Cattini C, Rendón J, de Oliveira JM (2009b) Ecological risk assessment of PCBs and other organic contaminant residues in laguna de terminos, mexico. Ecotoxicology 18:403–416
Castañeda-Chávez MR (2011) DDT in Crassostrea virginica (Gmelin, 1791) of coastal lagoons in the Gulf of Mexico. J Agric Sci 3:183–193
CCME (2008) Canadian water quality guidelines for the protection of aquatic life: Chlorpyrifos. In: Canadian environmental quality guidelines, 1999, Canadian Council of Ministers of the Environment, Winnipeg (Canada), pp. 9
Cogua P, Campos-Campos NH, Duque G (2012) Concentración de mercurio total y metilmercurio en sedimento y seston de la Bahía de Cartagena, Caribe colombiano. Bol Investig Mar y Costeras 41:267–285
Cordy P, Veiga MM, Salih I, Al-Saadi S, Console S, Garcia O, Mesa LA, Velásquez-López PC, Roeser M (2011) Mercury contamination from artisanal gold mining in Antioquia, Colombia: the world’s highest per capita mercury pollution. Sci Tot Envir 410–411:154–160
Daam MA, Van Den Brink PJ (2010) Implications of differences between temperate and tropical freshwater ecosystems for the ecological risk assessment of pesticides. Ecotoxicology 19:24–37
Davies IM (2004) Background/reference concentrations (BRCS) for the UK. Fisheries research services contract report no 05/04, Aberdeen.
de Brito APX, De Andrade Brüning IMR, Moreira I (2002) Chlorinated pesticides in mussels from Guanabara Bay, Rio de Janeiro, Brazil. Mar Pollut Bull 44:79–81
de Souza AS, Torres JPM, Meire RO, Neves RC, Couri MS, Serejo CS (2009) Organochlorine pesticides (OCs) and polychlorinated biphenyls (PCBs) in sediments and crabs (Chasmagnathus granulata, Dana, 1851) from mangroves of Guanabara Bay, Rio de Janeiro state, Brazil. Analysis 73:1–18
Dumailo S (2003) Evaluación de la problemática ambiental por medio del estudio de los fenómenos de sedimentación y contaminación en la Laguna de Bluefields, RAAS, Nicaragua. MSc Thesis, Univ Nac Aut Nicaragua.
Ebanks-Mongalo BF, Suárez-Sánchez J, Siu-Estrada E, Montoya-Arguello JJ, Mairena-Valdivia DA, Flores-Pacheco A, Van der Wal JC, Valencia-Quintana P (2013) Concentración de plaguicidas en agua, sedimentos y ostiones (Crassostrea rizophorae) de la Laguna de Bluefields, RAAS. Nicaragua WANI:49–54
Fernandez A, Singh A, Jaffé R (2007) A literature review on trace metals and organic compounds of anthropogenic origin in the Wider Caribbean Region. Mar Pollut Bull 54:1681–1691
Fox GA (2001) Wildlife as sentinels of human health effects in the Great Lakes—St. Lawrence basin. Environ Health Perspect 109:853–861
Frías-Espericueta MG, Osuna-López I, Bañuelos-Vargas I, López-López G, Muy-Rangel MD, Izaguirre-Fierro G, Rubio-Carrasco W, Meza-Guerrero PC, Voltolina D (2009) Cadmium, copper, lead and zinc contents of the mangrove oyster, Crassostrea corteziensis, of seven coastal lagoons of NW Mexico. Bull Environ Contam Toxicol 83:595–599
Galvao P, Henkelmann B, Longo R, Dorneles PR, Torres JPM, Malm O, Schramm KW (2014) Partition of organochlorine concentrations among suspended solids, sediments and brown mussel Perna perna, in tropical bays. Chemosphere 114:9–15
García F, Palacio C, Garcia U (2012) Water quality at Santa Marta coastal area (Colombia). Dyna 79:85–94
Gaspare L, Machiwa JF, Mdachi SJM, Streck G, Brack W (2009) Polycyclic aromatic hydrocarbon (PAH) contamination of surface sediments and oysters from the inter-tidal areas of Dar es Salaam, Tanzania. Environ Pollut 157:24–34
Gatermann R, Hellou J, Huhnerfuss H, Rimkus G, Zitko V (1999) Polycyclic and nitro musks in the environment: a comparison between Canadian and European aquatic biota. Chemosphere 38:3431–3441
GEF-REPCar (2011) Agricultural pesticide residues in Caribbean coastal waters. Colombia, Costa Rica and Nicaragua 2008–2011. GEF-REPCar Rpt UNEP, pp. 63
GESAMP (2001) Protecting the oceans from land-based activities—land-based sources and activities affecting the quality and uses of the marine, coastal and associated freshwater environment, Rep. Stud. GESAMP No. 71. UNEP, Nairobi
Giri C, Ochieng E, Tieszen LL, Zhu Z, Singh A, Loveland T, Masek J, Duke N (2011) Status and distribution of mangrove forests of the world using earth observation satellite data. Glob Ecol Biogeogr 20:154–159
Goldberg ED (1975) The Mussel Watch: a first step in global marine monitoring. Mar Pollut Bull 6:111
Gómez-Giraldo A, Osorio A, Toro FM, Osorio JD, Alvarez OA, Arrieta A (2009) Circulation pattern in the “Barbacoas” bay and its influence on sediment transport to the “Rosario” islands. Avances Rec Hidraul 20:21–40
Green NW, Schøyen M, Øxnevad S, Ruus A, Høgåsen T, Beylich B, Håvardstun J, Rogne ÅKG, Tveiten L (2012) Hazardous Substances in Fjords and Coastal Waters e 2011. Levels, trends and effects. Long-term monitoring of environmental quality in Norwegian coastal waters. NIVA.
Hellou J, Upshall C, Payne JF, Naidu S, Paranjape MA (1993) Total unsaturated-compounds and polycyclic aromatic-hydrocarbons in mollusks collected from waters around Newfoundland. Arch Environ Contam Toxicol 24:249–257
IARC (1987) Monographs on the evaluation of the carcinogenic risk of chemicals to humans. In: Overall evaluation of carcinogenicity: an updating of IAPC monographs Vols 1–42. International Agency for Research on Cancer, Lyon, France (Suppl. 7).
Jara-Marini ME, Soto-Jiménez MF, Páez-Osuna F (2008) Trace metals accumulation patterns in a mangrove lagoon ecosystem, Mazatlán Harbor, southeast Gulf of California. J Envir Sci Hlth 43A:995–1005
Kanhai LDK, Gobin JF, Beckles DM, Lauckner B, Mohammed A (2014) Metals in sediments and mangrove oysters (Crassostrea rhizophorae) from the Caroni Swamp, Trinidad. Environ Monit Assess 186:1961–1976
Kanhai LDK, Gobin JF, Beckles DM, Lauckner B, Mohammed A (2015) Polycyclic aromatic hydrocarbons (PAHs) in Crassostrea rhizophorae and Cathorops spixii from the Caroni Swamp, Trinidad, West Indies. Environ Sci Pollut Res 22:1366–1379
Kannan N, Reusch TBH, Schulz-Bull DE, Petrick G, Duinker JC (1995) Chlorobyphenyls: model compounds for metabolism in food chain organisms and their potential use as ecotoxicological stress indicators by application of the metabolic slope concept. Environ Sci Technol 29:1851–1859
Kimbrough KL, Johnson WE, Lauenstein GG, Christensen JD, Apeti DA (2008) An assessment of two decades of contaminant monitoring in the nation’s coastal zone. NOAA Technical Memorandum NOS NCCOS 74, pp. 118
Kimbrough KL, Johnson WE, Lauenstein GG, Christensen JD, Apeti DA (2009) An assessment of polybrominated diphenyl ethers (PBDEs) in sediments and bivalves of the U.S. coastal zone. Silver Spring, MD. NOAA Technical Memorandum NOS NCCOS 94. pp. 87
Lewis M, Pryor R, Wilking L (2011) Fate and effect of anthropogenic chemicals in mangrove ecosystems: a review. Envir Pollut 159:2328–2346
Liebezeit G, Brepohl D, Rizzi J, Guebert F, Krome M, MacHado E, Pijanowska U (2011) DDT in biota of Paranaguá Bay, Southern Brazil: recent input and rapid degradation. Water Air Soil Pollut 220:181–188
MARENA (2010). Caracterización de la cuenca No. 61. Río Escondido. Ministerio del Ambiente y los Recursos Naturales de Nicaragua, DGPN & DRHCH, pp. 38
Masson S, Couillard Y, Campbell PGC, Olsen C, Pinel-Alloul B, Perceval O (2010) Responses of two sentinel species (Hexagenia limbata—mayfly; Pyganodon grandis—bivalve) along spatial cadmium gradients in lakes and rivers in northwestern Québec. J Environ Monit 12:143–158
Monirith I, Ueno D, Takahashi S, Nakata H, Sudaryanto A, Subramanian A, Karuppiah S, Ismail A, Muchtar M, Zheng J, Richardson B, Puidente M, Hue ND, Tana TS, Tkalin AV, Tanabe S (2003) Asia–Pacific mussel watch: monitoring contamination of persistent organochlorine compounds in coastal waters of Asian countries. Mar Pollut Bull 46:281–300
Moon H-B, Kannan K, Lee S-J, Choi M (2007) Polybrominated diphenyl ethers (PBDEs) in sediment and bivalves from Korean coastal waters. Chemosphere 66:243–251
Nagelkerken I, Blaber SJM, Bouillon S, Green P, Haywood M, Kirton LG, Meynecke JO, Pawlik J, Penrose HM, Sasekumar A, Somerfield PJ (2008) The habitat function of mangroves for terrestrial and marine fauna: a review. Aquat Bot 89:155–185
Nascimento IA, Leite MBN, Sansone G, Pereira SA, Smith DH (1998) Stress protein accumulation as an indicator of impact by the petroleum industry in Todos os Santos Bay, Brazil. Aquat Ecosyst Health Manag 1:101–108
Navarro P, Bartolomé L, Raposo JC, Zuloaga O, Arana G, Etxebarria N (2010) Preparation of a reference mussel tissue material for polycyclic aromatic hydrocarbons and trace metals determination. Anal Chim Acta 675:91–96
Neff JM, Stout SA, Gunster DG (2005) Ecological risk assessment of polycyclic aromatic hydrocarbons in sediments: identifying sources and ecological hazards. Integr Environ Assess Manag 1:22–33
Nhan DD, Carvalho FP, Am NM, Tuan NQ, Yen NTH, Villeneuve J-P, Cattini C (2001) Chlorinated pesticides and PCBs in sediments and molluscs from freshwater canals in the Hanoi region. Environ Pollut112:311–320.
Oros DR, Ross JRM (2004) Polycyclic aromatic hydrocarbons in San Francisco Estuary sediments. Mar Chem 86:169–184
Oros DR, Ross JRM (2005) Polycyclic aromatic hydrocarbons in bivalves from the San Francisco estuary: spatial distributions, temporal trends, and sources (1993-2001). Mar Environ Res 60:466–488
Oros DR, Ross JRM, Spies RB, Mumley T (2007) Polycyclic aromatic hydrocarbon (PAH) contamination in San Francisco Bay: a 10-year retrospective of monitoring in an urbanized estuary. Environ Res 105:101–118
OSPAR Commission (2009) Background document on CEMP assessment criteria for QSR 2010. In: Monitoring and Assessment Series. OSPAR Commission. London
OSPAR Commission (2010) Quality Status Report 2010. OSPAR Commission, London.
OSPAR Commission (2012) Environmental Assessment Criteria (EACs) for hazardous substances in the marine environment: OSPAR contribution to addressing the challenge of assessing chemical quality across all marine waters. OSPAR Commission, London.
OSPAR Commission (2013) Levels and trends in marine contaminants and their biological effects—CEMP Assessment report 2012. OSPAR Commission, London
OSPARCommission (2005) Agreement on background concentrations for contaminants in seawater, biota and sediment. OSPAR Agreement 2005-6, London, pp 4
Osuna-Martínez CC, Páez-Osuna F, Alonso-Rodríguez R (2011) Cadmium, copper, lead and zinc in cultured oysters under two contrasting climatic conditions in coastal lagoons from SE Gulf of California, Mexico. Bull Environ Contam Toxicol 87:272–275
Páez-Osuna F, Osuna-Martínez CC (2015) Bioavailability of cadmium, copper, mercury, lead, and zinc in subtropical coastal lagoons from the southeast Gulf of California using mangrove oysters (Crassostrea corteziensis and Crassostrea palmula). Arch Environ Contam Toxicol 68:305–316
Perdomo L, Ensminger I, Espinosa LF, Elster C, Wallner-Kersanach M, Schnetter M-L (1998) The mangrove ecosystem of the Ciénaga Grande de Santa Marta (Colombia): observations on regeneration and trace metals in sediment. Mar Pollut Bull 37:393–403
Pereira WE, Hostettler FD, Luoma SN, van Geen A, Fuller CC, Anima RJ (1999) Sedimentary record of anthropogenic and biogenic polycyclic aromatic hydrocarbons in San Francisco Bay, California. Mar Chem 64:99–113
Rainbow PS (2006) Biomonitoring of trace metals in estuarine and marine environments. Australas J Ecotoxicol 12:107–122
Ramdine G, Fichet D, Louis M, Lemoine S (2012) Polycyclic aromatic hydrocarbons (PAHs) in surface sediment and oysters (Crassostrea rhizophorae) from mangrove of Guadeloupe: levels, bioavailability, and effects. Ecotox Environ Safety 79:80–89
Rawlins BG, Ferguson AJ, Chilton PJ, Arthurton RS, Rees JG, Baldock JW (1998) Review of agricultural pollution in the Caribbean with particular emphasis on small island developing states. Mar Pollut Bull 36:658–668
Rebelo MF, Rebouças do Amaral MC, Pfeiffer WC (2003) High Zn and Cd accumulation in the oyster Crassostrea rhizophorae, and its relevance as a sentinel species. Mar Pollut Bull 46:1354–1358.
Rebelo MF, Amaral MCR, Pfeiffer WC (2005) Oyster condition index in Crassostrea rhizophorae (Guilding 1828) from a heavy-metal polluted coastal lagoon. Braz J Biol 65:345–351
Rimkus GG (1999) Polycyclic musk fragrances in the aquatic environment. Toxicol Lett 111:37–56
Rojas de Astudillo L, Yen IC, Bekele I (2005) Heavy metals in sediments, mussels and oysters from Trinidad and Venezuela. Rev Biol Trop 53:41–51
Rüdel H, Böhmer W, Schröter-Kermani C (2006) Retrospective monitoring of synthetic musk compounds in aquatic biota from German rivers and coastal areas. J Environ Monit 8:812–823
Sericano JL, Wade TL, Jackson TJ, Brooks JM, Tripp BW, Farrington JW, Mee LD, Readmann JW, Villeneuve JP, Goldberg ED (1995) Trace organic contamination in the Americas: an overview of the US National Status & Trends and the International “Mussel Watch” programmes. Mar Pollut Bull 31:214–225
Serrano R, López FJ, Hernández F, Peña JB (1997) Bioconcentration of chlorpyrifos, chlorfenvinphos, and methidathion in Mytilus galloprovincialis. Bull Environ Contam Toxicol 59:968–975
Silva CAR, Rainbow PS, Smith BD, Santos ZL (2001) Biomonitoring of trace metal contamination in the Potengi estuary, Natal (Brazil), using the oyster Crassostrea rhizophorae, a local food source. Water Res 35:4072–4078
Silva CAR, Rainbow PS, Smith BD (2003) Biomonitoring of trace metal contamination in mangrove-lined Brazilian coastal systems using the oyster Crassostrea rhizophorae: comparative study of regions. Hydrobiologia 501:199–206
Silva CAR, Smith BD, Rainbow PS (2006) Comparative biomonitors of coastal trace metal contamination in tropical South America (N. Brazil). Mar Envir Res 61:439–455
Siung-Chang A (1997) A review of marine pollution issues in the Caribbean. Environ Geochem Health 19:45–55
Soclo HH, Garrigues P, Ewald M (2000) Origin of polycyclic aromatic hydrocarbons (PAHs) in coastal marine sediments: case studies in Cotonou (Benin) and Aquitaine (France) areas. Mar Pollut Bull 40:387–396
Solaun O, Rodríguez JG, Borja A, González M, Saiz-Salinas JI (2013) Biomonitoring of metals under the water framework directive: detecting temporal trends and abrupt changes, in relation to the removal of pollution sources. Mar Pollut Bull 67:26–35
Tomlinson DL, Wilson JG, Harris CR, Jeffrey DW (1980) Problems in assessment of heavy metals in estuaries and the formation of pollution index. Helgol Meeresunters 33:566–575
Torres RJ, Cesar A, Pereira CDS, Choueri RB, Abessa DMS, do Nascimento MRL, Fadini PS, Mozeto AA (2012) Bioaccumulation of polycyclic aromatic hydrocarbons and mercury in oysters (Crassostrea rhizophorae) from two Brazilian estuarine zones. Int J Oceanogr; 8 pp; ID 838320; doi: 10.1155/2012/838320.
UNEP (1994) Regional overview of land-based sources of pollution in the Wider Caribbean Region. UNEP(OCA)/CAR WG 14/4, 55 pp.
UNEP (2002) Central America and the Caribbean regional report, regionally based assessment of persistent toxic substances. UNEP, CH-1219, Geneva-Switzerland 133 pp.
UNEP (2004) Global International Water Assessment (GIWA), Caribbean Sea/Colombia & Venezuela, Central America & Mexico. GIWA Regional Assessment 3b, 3c. University of Kalmar, Kalmar, Sweden.
UNEP (2006) Isaza, C.F.A., Sierra-Correa, P.C., Bernal-Velasquez,M., Londono, L.M. and W. Troncoso. Caribbean Sea/Colombia & Venezuela, Caribbean Sea/Central America & Mexico. GIWA Regional Assessment 3b, 3c. University of Kalmar, Kalmar, Sweden.
USEPA (2001) Guidance for reporting toxic chemicals: polycyclic aromatic compounds category, EPA 260-B-01-03. Washington, DC, 40 pp
Valdez Domingos FX, Azevedo M, Silva MD, Randi MAF, Freire CA, Silva de Assis HC, Oliveira Ribeiro CA (2007) Multibiomarker assessment of three Brazilian estuaries using oysters as bioindicators. Environ Res 105:350–363
Van Lavieren H, Metcalfe CD, Drouillard K, Sale PF, Bouchot GG, Reid R, Vermeulen L (2011) Strengthening coastal pollution management in the wider Caribbean region. Proc 64th Gulf Caribb Fish Inst 5:1–11
Villeneuve JP, Carvalho FP, Fowler SW, Cattini C (1999) Levels and trends of PCBs, chlorinated pesticides and petroleum hydrocarbons in mussels from the NW Mediterranean coast: comparison of concentrations in 1973/1974 and 1988/1989. Sci Total Environ 237-238:57–65
Vivas-Aguas L, Tosic M, Sánchez J, Narváez S, Cadavid B, Bautista P, Betancourt J, Parra J, Echeverri L, Espinosa L (2010) Diagnóstico y evaluación de la calidad ambiental marina en el Caribe y Pacifico colombiano. REDCAM Inf Téc 2010. ppMAR. Santa Marta, pp. 208
Vivas-Aguas L, Sánchez J, Betancourt J, Quintero M, Moreno Y, Santana C, Cuadrado I, Ibarra K, Rios M, Obando P, Sánchez D (2013) Diagnóstico y evaluación de la calidad ambiental marina en el Caribe y Pacifico colombiano. REDCAM Inf Téc 2014. INVEMAR. Santa Marta, 314 pp.
Wade TL, Sericano JL, Gardinali PR, Wolff G, Chambers L (1998) NOAA’s ‘Mussel Watch’ Project: current use organic compounds in bivalves. Mar Pollut Bull 37:20–26
Wallner-Kersanach M, Theede H, Eversberg U, Lobo S (2000) Accumulation and elimination of trace metals in a transplantation experiment with Crassostrea rhizophorae. Arch Environ Contam Toxicol 38:40–45
Yunker MB, Macdonald RW, Vingarzan R, Mitchell RH, Goyette D, Sylvestre S (2002) PAHs in the Fraser River basin: a critical appraisal of PAH ratios as indicators of PAH source and composition. Organic Geochem 33:489–515
Zaccaron da Silva A, Zanette J, Ferreira JB, Guzenski J, Freire Marques MR, Bainy ACD (2005) Effects of salinity on biomarker responses in Crassostrea rhizophorae (Mollusca, Bivalvia) exposed to diesel oil. Ecotox Envir Safety 62:376–382
Zampoukas N et al. (2014) Technical guidance on monitoring for the Marine Strategy Framework Directive. JRC Scientific and Policy Reports, Reports EUR 26499 EN. ISBN 978–92–79-35426-7.
Ziarrusta H, Olivares M, Delgado A, Posada-Ureta O, Zuloaga O, Etxebarria N (2015) Multiscreening determination of organic pollutants in molluscs using matrix solid phase dispersion. J Chromatogr 1391A:18–30
Acknowledgements
The authors are indebted to Drs L Garmendia and M Ortiz-Zarragoitia from PiE-UPV/EHU, to Dr. L Villamil, A Moncaleano and S Cáceres from UJTL and to colleagues from the Department of Biology (Environ Educ Prog, UNAN-León) for their invaluable assistance during sampling. This work was funded by the Spanish Agency for International Development Cooperation (CARIBIOPOL-AECID 11-CAP2-1595) and supported by the Spanish Ministry of Economy and Finances (BMW-CTM2012-40203-C02-01), by The University of the Basque Country UPV/EHU (UFI 11/37), and by the Basque Government through Consolidated Research Groups fellowship (IT810-B). The authors also want to thank the scientific staff of the Department of Biology from Bluefields Indian and Caribbean University (BICU) for their support in the logistic and sampling strategy, as well as the Research Center on Health, Work, and Environment (CISTA, UNAN-León) for their collaboration in the pretreatment of samples for chemical analysis.
Author information
Authors and Affiliations
Corresponding author
Additional information
Responsible editor: Hongwen Sun
Rights and permissions
About this article
Cite this article
Aguirre-Rubí, J.R., Luna-Acosta, A., Etxebarría, N. et al. Chemical contamination assessment in mangrove-lined Caribbean coastal systems using the oyster Crassostrea rhizophorae as biomonitor species. Environ Sci Pollut Res 25, 13396–13415 (2018). https://doi.org/10.1007/s11356-017-9159-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11356-017-9159-2