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PAHs impacts on aquatic organisms: contamination and risk assessment of seafood following an oil spill accident

Abstract

Oil spills, intrinsically related to the petroleum production chain, represent a risk to the marine environment and a potential threat to humans through seafood consumption. We revised the NE Brazil oil spill and other accidents along the Brazilian coast, with a focus on seafood contamination, covering topics such as bioaccumulation, bioaccessibility, and risk analysis. Comprehensive knowledge of the impacts of spills helps in the interpretation of the dynamics of hydrocarbons released into the sea, contributing to actions to control their negative impacts. Currently, no legal limits have been established permanently in Brazil for PAHs in seafood edible tissues.

Key words
bioaccumulation; Brazilian seafood; human health; oil spill; PAH; toxicity

INTRODUCTION

The land-sea transition region encompasses various ecosystems, connecting rivers, estuaries, bays, and the coastal ocean (Bauer et al. 2013BAUER JE, CAI W-J, RAYMOND PA, BIANCHI TS, HOPKINSON CS REGNIER PAG. 2013. The changing carbon cycle of the coastal ocean. Nature 504: 61-70.). Features such as high rates of primary and secondary productions, high abundance, and biodiversity of flora and fauna are examples of many marine ecosystem services used by humans to build their well-being. Consequently, it results in the attraction and settlement of over 38% of the World’s population in the coastal zone (Unep 2014UNEP - UNITED NATIONS ENVIRONMENT PROGRAMME. 2014. The UNEP Environmental Data Explorer, as compiled from UNEP/DEWA/GRID-Geneva. UNEP, Geneva. http://geodata.grid.unep.ch.
http://geodata.grid.unep.ch...
). Indeed, human activities are recognized as posing threats to the health of major Earth systems, including the ocean and its coastal zone, at local, regional, and/or global scales (Ekins et al. 2019EKINS P, GUPTA J BOILEAU P. 2019. Global Environment Outlook GEO-6. Cambridge University Press, 745 p.).

Developments in the fossil fuel industry - in pace with modern society’s demand for energy - have the potential to affect coastal ocean ecosystems and human health (Patin 1999PATIN S. 1999. Environmental impact of the offshore oil and gas industry. EcoMonitor Publishing: New York.). Most of the oil (and related refined products) directly affecting coastal (and marine) ecosystems come from chronic inputs, and are related to the oil and gas exploration, production, transportation, refining, and use (NRC 2003NRC. 2003. Oil in the Sea - inputs, fates and effects, 2nd ed., National Academy Press: Washington.). However, acute events of large oil spills also have negative environmental consequences, as observed in the case of the Deep-Water Horizon rig blowout (Ramseur 2010RAMSEUR JL. 2010. Deepwater Horizon Oil Spill: The Fate of the Oil. Congressional Research Service.) or the Exxon Valdez in Alaska (Peterson et al. 2003PETERSON CH, RICE SD, SHORT JW, ESLER D, BODKIN JL, BALLACHEY BE IRONS DB. 2003. Long-Term Ecosystem Response to the Exxon Valdez Oil Spill. Science 302: 2082-2086.), just to name a few examples. Social and economic impacts are also relevant aspects in the case of a coastal oil spill, including a drastic drop in revenues from tourism and fisheries marketing by local traditional communities and the contamination of seafood (Storelli et al. 2013STORELLI MM, BARONE G, PERRONE VG STORELLI A. 2013. Risk characterization for polycyclic aromatic hydrocarbons and toxic metals associated with fish consumption. J Food Compos Anal 31: 115-119., Wenzl Zelinkova 2019).

In a scenario of the high environmental and socio-economic vulnerability of coastal locations and the human population affected by an oil spill, negative impacts can be aggravated due to the different social groups directly impacted by such accidents, the activities affected, and the profile of the compounds present in the oil and their persistence and bioaccumulation in the marine environment (Fattal et al. 2010FATTAL P, MAANAN M, TILLIER I, ROLLO N, ROBIN M POTTIER P. 2010. Coastal Vulnerability to Oil Spill Pollution: the Case of Noirmoutier Island (France). J Coast Res 26: 879-887., Duran Cravo-Laureau 2016DURAN R CRAVO-LAUREAU C. 2016. Role of environmental factors and microorganisms in determining the fate of polycyclic aromatic hydrocarbons in the marine environment. FEMS Microbiology Reviews 40: 814-830.).

Petroleum and its products are sources of PAHs that are characterized by a predominance of 2-3 rings and alkyl homologs in the naphthalene, phenanthrene, dibenzothiophene, and chrysene series (Tissot Welt 1984TISSOT BP WELT DH. 1984. Petroleum formation and occurrence. Springer-Verlag, 679 p., Wang et al. 2003WANG Z, HOLLEBONE B, FINGAS M, SIGOUIN L, LANDRIAULT M, SMITH P, NOONAN J THOUIN G. 2003. Characteristics of spilled oils, fuels, and petroleum products: 1. Composition and properties of selected oils. EPA/600/R-03/072, US Environmental Protection Agency, Washington, DC.). Another important origin of polyaromatic compounds includes the combustion of fossil fuels and biomass burning, which produces non-alkylated compounds with 4-6 rings known as pyrogenic PAHs (Wang et al. 1999WANG Z, FINGAS M PAGE DS. 1999. Oil spill identification. Journal of Chromatography A 843: 369-411.). The distinct molecular distribution of PAHs is used as tool for assigning sources of petrogenic and/or pyrolytic compounds in the atmosphere, water, sediments, and biological tissues (Tsapakis Stephanou 2005TSAPAKIS M STEPHANOU E. 2005. Polycyclic Aromatic Hydrocarbons in the Atmosphere of the Eastern Mediterranean. Environ Sci Technol 39: 6584-6590., Mirza et al. 2012MIRZA R, MOHAMMADI M, SOHRAB AD, SAFAHIEH A, SAVARI A HAJEB P. 2012. Polycyclic Aromatic Hydrocarbons in Seawater, Sediment, and Rock Oyster Saccostrea cucullata from the Northern Part of the Persian Gulf (Bushehr Province). Water Air Soil Pollut 223: 189-198., Asagbra et al. 2015ASAGBRA MC, ADEBAYO AS, ANUMUDU CI, UGWUMBA OA UGWUMBAC AAA. 2015. Polycyclic aromatic hydrocarbons in water, sediment and fish from the Warri River at Ubeji, Niger Delta, Nigeria. Afr J Aquat Sci 2015: 1-7., Sun et al. 2016SUN R-X, LIN Q, KE C-L, DU F-Y, GU Y-G, CAO K, LUO K-J MAI B-X. 2016. Polycyclic aromatic hydrocarbons in surface sediments and marineorganisms from the Daya Bay, South China. Mari Poll Bull 103: 325-332.). For example, bivalves collected near water discharge platforms show enhanced levels of naphthalenes, phenanthrenes, or dibenzothiophenes, all characteristic of petroleum (Neff et al. 2011NEFF J, LEE K DEBLOIS EM. 2011. Produced Water: Overview of Composition, Fates, and Effects, in: Lee K Neff J (Eds), Produced Water: Environmental Risks and Advances in Mitigation Technologies. Springer New York, 3-54 p.). A similar bioaccumulation profile of petroleum-derived PAHs is also observed in Guanabara Bay, an oil-residue chronically impacted bay surrounded by the Rio de Janeiro metropolitan region (Francioni et al. 2005FRANCIONI E, WAGENER A, SCOFIELD AL CAVALIER B. 2005. Biomonitoring of polycyclic aromatic hydrocarbon in Perna perna from Guanabara Bay, Brazil. Environ. Forensics 6: 361-370., Ramos et al. 2017RAMOS AB, FARIAS CO, HAMACHER C ARAUJO M. 2017. Assessment of PAHs occurrence and distribution in brown mussels (Perna perna Linnaeus 1758) subject to different levels of contamination in Brazil. Reg Stud 14: 145-151.).

The fisheries body-burden of contaminants in affected areas includes a myriad of organic compounds and inorganic elements (including radioactive) that are present in crude oils (Barescut et al. 2009BARESCUT J, ERIKSEN D, SIDHU R, RAMSØY T, STRÅLBERG E, IDEN K BERNTSSEN M. 2009. Radioactivity in produced water from Norwegian oil and gas installations – concentrations, bioavailability, and doses to marine biota. Radioprotection 44: 869-874., Jisr et al. 2020JISR N ET AL. 2020. Levels of heavy metals, total petroleum hydrocarbons, and microbial load in commercially valuable fish from the marine area of Tripoli, Lebanon. Environ Monit Assess 192: 705., Ilori Chetty 2021ILORI AO CHETTY N. 2021. Activity concentrations and radiological hazard assessments of 226Ra, 232Th, and 40K in soil samples of oil-producing areas of South Africa. Int J Environ Health Res 3: 1-13.). Herein, the focus will be on organic compounds, particularly those with a cyclic aromatic structure. In petroleum, the mono-cyclic aromatic hydrocarbons, namely benzene, toluene, ethylbenzene, and isomers of xylenes (the BTEX fraction) are abundant components but also highly volatile and cause short-term impacts (Neff et al. 2011NEFF J, LEE K DEBLOIS EM. 2011. Produced Water: Overview of Composition, Fates, and Effects, in: Lee K Neff J (Eds), Produced Water: Environmental Risks and Advances in Mitigation Technologies. Springer New York, 3-54 p.). In contrast, compounds with two up to six-fused benzene rings, known collectively as the polycyclic aromatic hydrocarbons (PAHs) (Anderson Achten 2015, Stout et al. 2015STOUT SA, EMSBO-MATTINGLY SD, DOUGLAS GS, UHLER AD MCCARTHY KJ. 2015. Beyond 16 Priority Pollutant PAHs: A Review of PACs used in Environmental Forensic Chemistry. Polycyclic Aromat Compd 35: 285-315.), are of environmental relevance because they are ubiquitous and persistent in aquatic systems, bioaccumulate through the chain food and can act as agents of endocrine disruption, mutagenicity (IARC 2010IARC. 2010. Some non-heterocyclic polycyclic aromatic hydrocarbons and some related exposures. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, p. 773., Bergman et al. 2013BERGMAN A, HEINDEL JJ, JOBLING S, KIDD KA ZOELLER T. 2013. State of the Science Endocrine Disrupting Chemicals - 2012. World Health Organization.) and/or carcinogenicity (Hwang et al. 2012HWANG K, WOO S, CHOI J KIM M. 2012. Survey of polycyclic aromatic hydrocarbons in marine products in Korea using G. C. / M. S. Food Additives Contaminants Part B,1-7.). In addition, the recognition of the adverse effects of PAHs on human health has resulted in the establishment by government agencies of threshold levels that guarantee the safety of seafood for human consumption, as will be detailed later.

Here, the impact of PAHs derived from the oil spill on fisheries and food safety in coastal systems is addressed. The main goal is to gather information on these subjects obtained following the recent major oil spills around the world, with a focus on the Brazilian scenario. The information available in the country on these subjects, following the mysterious oil spill (Lourenço et al. 2020LOURENÇO RA, COMBI T, ALEXANDRE MR, SASAKI ST, ZANARDI-LARMARDO E YOUGUI GT. 2020. Mysterious oil spill along Brazil’s northeast and southeast seaboard (2019-2020): Trying to find answers and filling data gaps. Mar Poll Bull 156: 111219.) that hit the NE Brazilian coast from August 2019 through January 2020 (Soares et al. 2020SOARES MDO ET AL. 2020. Oil spill in South Atlantic (Brazil): Environmental and governmental disaster. Mar. Policy 115: 103879.) was compiled to help understand the dynamics of hydrocarbons released at sea and their potential environmental and socio-economic impacts on the coastal zone and local communities. The purpose of this review is to help guide emergency actions in the aftermath of the oil spill in Brazil, as well as to support the design of public programs and communication to fishermen and consumers about the environmental impacts of oil spills.

Oil spill accidents

Brazil is a reference in oil exploration from marine sources and is also a route for transporting oil from neighbouring countries. In 2020, the average oil production in the country reached 2.94 million barrels per day, while natural gas reached 127 million cubic meters per day (Petrobras 2020PETROBRAS. 2020. Available in: https://www.petrobras.com.br/pt/nossas23atividades/areas-de-atuacao/exploracao-e-producao-de-petroleo-e-gas/pre-sal/
https://www.petrobras.com.br/pt/nossas23...
). This high oil production presents associated risks and demands from the petroleum industry, among other environmental requirements, an Individual Emergency Plan (PEI) to prevent accidents and control/mitigate the environmental impacts in the aftermath (Brasil 2019BRASIL. 2019. Marinha, Exército, Corpo de Bombeiros e Ibama atuam no combate às manchas de óleo no Nordeste. Ibama, 05 de nov. de 2019. Available in: https://www.gov.br/defesa/pt-br/assuntos/noticias/ultimas-noticias/marinha-exercito-corpode-bombeiros-e-ibama-atuam-no-combate-as-manchas-de-oleo-no-nordeste.
https://www.gov.br/defesa/pt-br/assuntos...
).

In Brazil, oil accidents have been reported in many parts of the country. Back in the 1970s, three accidents of great magnitude were reported: (i) the Takimyia Maru vessel (1974) in the São Sebastião channel, in the state of São Paulo; (ii) the Brazilian Marina (1978) vessel in Rio de Janeiro, in Guanabara Bay (1975), and: (iii) in 2001, when the P36 oil exploration platform in the Campos Basin in Rio de Janeiro caught fire and sank, 1,300 m³ of gas and 350 m³ of oil were spilled (Cetesb 2012CETESB. 2012. Breve história do petróleo no Brasil e em São Paulo e principais acidentes. Cetesb, SP. Available in: https://cetesb.sp.gov.br/emergencias-quimicas/wp-content/uploads/sites/22/2013/12/Principais-Acidentes-Brasil-.pdf.
https://cetesb.sp.gov.br/emergencias-qui...
).

In 2000, Guanabara Bay in Rio de Janeiro was once again affected by an oil spill, the rupture of an oil pipeline leaked approximately 1,300 m3 of marine fuel (Meniconi et al. 2001MENICONI MFG, SANTOS AF, SALMITO TMC, ROMÃO CM, MOREIRA IMNS SCOFIELD AL, AZEVEDO LAC MACHADO GAWC. 2001. Fisheries safety monitoring in the Guanabara Bay, Brazil following a marine fuel oil spill. API 2001: 951-957.). In 2004, in the state of Paraná (South Brazil), the explosion of the Chilean Vicuña vessel caused the spilling of millions of litters of bunker oil in the Paranaguá Port, which affected four municipalities and caused the paralysis of fishing for two months (Noernberg et al. 2008NOERNBERG MA, ANGELOTTI R, CALDEIRA GA DE SOUSA AR. 2008. Environmental sensitivity assessment of Paraná coast for oil spill. Braz J Aquat Sci Technol 12: 49-59.). In 2011, another environmental contamination caused by the spill of 3,700 oil barrels, covered 182 km² of an area of Campos Bay (Matos et al. 2019MATOS DL, CUNHA DR CUTRIM S. 2019. Diagnóstico dos acidentes envolvendo derrame de óleo ao mar no complexo portuário de São Luís. In: VI Congresso Internacional de Desempenho Portuário, Florianópolis, Brasil.). In Pará, in 2015, in the northern region of Brazil, a ship carrying around five thousand oxen sank and spilled about 135 m³ of oil into the Pará river, in the city of Barcarena. Most of the animals that were to be transported drowned and the oil spilled into the river to such an extent that there was no longer any visual evidence of their presence (O’Briens 2016O’BRIENS BRASIL. 2016. Naufrágio do Navio Haidar - Baía do Capim/ PA. Relatório Unificado - Projetos ambientais. www.wittobriens.com.br.
www.wittobriens.com.br...
, Oceana 2020OCEANA. 2020. Governo e indústria dos EUA não aprenderam com o maior vazamento de petróleo do país - e o Brasil?. [SI]. Oceana Brasil, 08 de mai. de 2020. Disponível em: https://brasil.oceana.org/pt-br/imprensa/comunicados-a-imprensa/governo-eindustria-dos-eua-nao-aprenderam-com-o-maior-vazamento-de.
https://brasil.oceana.org/pt-br/imprensa...
). Matos et al. (2019)MATOS DL, CUNHA DR CUTRIM S. 2019. Diagnóstico dos acidentes envolvendo derrame de óleo ao mar no complexo portuário de São Luís. In: VI Congresso Internacional de Desempenho Portuário, Florianópolis, Brasil. reported several accidents with oil spills in the state of Maranhão (Northeast). In another accident in the Northeast region, in 2015, the leakage of a pipeline connecting the PCM-5 and PCM-6 production vessels spilled 7,000 liters of oil into the sea, in the Bay of Sergipe-Alagoas (Brasil 2017BRASIL. 2017. Ibama multa Petrobras em R$ 2,5 milhões por derramamento de óleo no litoral de SE. Available in: https://www.gov.br/ibama/pt-br/assuntos/noticias/copy_of_noticias/noticias-2016/ibama-multa-petrobras-em-r-2-5-milhoes-por-derramamento-de-oleo-no-litoral-de-se.
https://www.gov.br/ibama/pt-br/assuntos/...
). In 2016, in the Sergipe State, Petrobras was fined for the spill of 1.8 tons of oil, which spread over 30 km in 3 days (Brasil 2017BRASIL. 2017. Ibama multa Petrobras em R$ 2,5 milhões por derramamento de óleo no litoral de SE. Available in: https://www.gov.br/ibama/pt-br/assuntos/noticias/copy_of_noticias/noticias-2016/ibama-multa-petrobras-em-r-2-5-milhoes-por-derramamento-de-oleo-no-litoral-de-se.
https://www.gov.br/ibama/pt-br/assuntos/...
). The causes of the accident are still unclear.

The Brazilian Institute for the Environment and Renewable Natural Resources (IBAMA) also reports several oil spill accidents. For instance, in February 2019, the rupture of a hose during the transfer of oil from the platform P-58 to the São Sebastião ship spilled oil on the coast of Espírito Santo state, SE of Brazil, that spread for 2.4 km; although the slick has been quickly dispersed, the environmental impact has not been measured yet (IBAMA 2019IBAMA. 2019. Vazamento na P-58 causa mancha de óleo a 85 km do litoral do ES. Available in: https://www.gov.br/ibama/pt-br/assuntos/notas/copy_of_notas/vazamento-na-p-58-causa-mancha-de-oleo-a-85-km-do-litoral-do-es.
https://www.gov.br/ibama/pt-br/assuntos/...
).

More recently, starting in August 2019 and extending for several months, the coastline of 11 states from the Northeast and the Southeast regions were hit by oil residues, causing social, human health, and environmental disruption (Pena et al. 2019PENA PGL, NORTHCROSS AL, LIMA MAG REGO RCF. 2019. Derramamento de óleo bruto na costa brasileira em 2019: emergência em saúde pública em questão. Cad Saúde Pública 36: e00231019.). This accident, already considered the biggest environmental disaster in Brazil, impacted 3,600 km of coastline, more than 980 beaches, and more than 5,000 tons of oiled wastes were removed from the marine and land areas (Brasil 2019BRASIL. 2019. Marinha, Exército, Corpo de Bombeiros e Ibama atuam no combate às manchas de óleo no Nordeste. Ibama, 05 de nov. de 2019. Available in: https://www.gov.br/defesa/pt-br/assuntos/noticias/ultimas-noticias/marinha-exercito-corpode-bombeiros-e-ibama-atuam-no-combate-as-manchas-de-oleo-no-nordeste.
https://www.gov.br/defesa/pt-br/assuntos...
, Soares et al. 2020SOARES MDO ET AL. 2020. Oil spill in South Atlantic (Brazil): Environmental and governmental disaster. Mar. Policy 115: 103879.). The Brazilian National Health Surveillance Agency (ANVISA) characterizes the product dumped on the coasts of Pernambuco and Paraíba as crude oil, before spreading to the Southeast Region, into the states of Espírito Santo and Rio de Janeiro (Carmo Teixeira 2020CARMO EH TEIXEIRA MG. 2020. Desastres tecnológicos e emergências de saúde pública: o caso do derramamento de óleo no litoral do Brasil. Cad Saúde Pública 36: e00234419.). Chemical analyses classified the oil as Venezuelan crude, but the accident’s origin and causes are not yet known (Disner Torres 2020DISNER GR TORRES M. 2020. The environmental impacts of 2019 oil spill on the Brazilian coast: Overview. Rev Bras Gest Amb Sust 7: 214-255.). According to reports, almost two years after the accident, oil stains reappeared on some Brazilian beaches (northeast) (Brasil de Fato 2020BRASIL DE FATO. 2020. Mais de um ano após vazamento de óleo em praias do Nordeste, danos ainda são sentidos. Available in: https://www.brasildefato.com.br/2020/10/13/mais-de-um-ano-apos-vazamento-de-oleo-em-praias-do-nordeste-danos-ainda-sao-sentidos.
https://www.brasildefato.com.br/2020/10/...
, Jornal da Band 2021JORNAL DA BAND. 2021. Manchas de óleo voltam a aparecer em praia da Bahia. Avaliable in: https://www.band.uol.com.br/noticias/jornal-da-band/ultimas/manchas-de-oleo-volta-a-aparecer-em-praia-da-bahia-16357384.
https://www.band.uol.com.br/noticias/jor...
). The medium and long-term impacts of the oil spill remain unpredictable.

PAHs toxicity

As previously mentioned, among the several hundreds of hydrocarbons found in petroleum, the major compounds of environmental concern – due to their negative impacts on the ecosystem and human health – are the aromatic ones, which may represent as much as 5% of crude oils (Hodson 2017HODSON PV. 2017. The toxicity to fish embryos of PAH in crude and refined oils. Arch Environ Contam Toxicol 73: 12-18.). Whereas the petroleum abundant monocyclic aromatics hydrocarbons (BTEX) are relevant only in the short-term impacts after an oil spill, as they are quickly transported to the atmosphere, the polycyclic aromatic hydrocarbons (PAHs), with two to at least 6 fused rings, are persistent and bioaccumulative toxicants (Neff 2002NEFF JM. 2002. Bioaccumulation in marine organisms: effects of contaminants from oil well produced water. Elsevier, 439 p.).

The toxicities of several PAHs are well established and, in the case of human health, are usually associated with several types of cancers and degenerative diseases (Albers 2003ALBERS PH. 2003. Petroleum and Individual Polycyclic Aromatic Hydrocarbons. In: Hoffman DJ, Rattner BA, Burton Jr GA Cairns Jr J (Eds), Handbook of Ecotoxicology, p. 342-346., Hamidi et al. 2016HAMIDI EN, HAJEB P, SELAMAT J RAZIS AFA. 2016. Polycyclic Aromatic Hydrocarbons (PAHs) and their Bioaccessibility in Meat: A Tool for Assessing Human Cancer Risk. APJCP 17: 15-23.). In wildlife, the negative effect of PAHs exposure includes, for example, reduction of marine plant diversity (Saifullah Chaghtai 2005SAIFULLAH SM CHAGHTAI F. 2005. Effect of “Tasman Spirit” oil spill on marine plants in the coastal area of Karachi. Int J Biol Biotech 2: 299-306.), hematopoietic disorders in oysters Crassostrea gigas (Donoghy et al. 2010DONOGHY L, HONG H-K, LEE H-J, JUN J-C, PARK Y-J CHOI K-S. 2010. Hemocyte parameters of the Pacifc oyster Crassostrea gigas a year after the Hebei Spirit oil spill of the west coast of Korea. Helgol Mar Res 64: 349-355.), and reduced functionality of the innate and acquired immune systems in fish (Reynaud Deschaux 2006REYNAUD S DESCHAUX P. 2006. The effects of polycyclic aromatic hydrocarbons on the immune system of fish: A review. Aquat Toxicol 77: 229-238.), among others.

The recognition of the risk associated with PAHs exposure has led the United States Environmental Protection Agency (EPA) to rank in the early 1970s sixteen compounds as priority pollutants. These included only non-alkylated with 2 to 6 fused rings PAHs, which reflected the limited analytical capability of quantifying PAHs in environmental samples, rather than the recognition of their intrinsic toxicities (Anderson Achten 2015ANDERSON JT ACHTEN C. 2015. Time to say goodbye to the 16 EPA PAHs? Toward an up-to-date use of PACs for environmental purposes. Polycyclic Aromat Compd 35: 330-354.). The list is now known to be limited in properly addressing the environmental fate and effect of PAHs in aquatic systems, and over forty individual PAHs, including parental and alkylated compounds, are included in such evaluations (Stout et al. 2015STOUT SA, EMSBO-MATTINGLY SD, DOUGLAS GS, UHLER AD MCCARTHY KJ. 2015. Beyond 16 Priority Pollutant PAHs: A Review of PACs used in Environmental Forensic Chemistry. Polycyclic Aromat Compd 35: 285-315., Boehm et al. 2018BOEHM PD, PIETARI J, COOK LL SABA T. 2018. Improving rigor in polycyclic aromatic hydrocarbon source fingerprinting. Environmental Forensics 19: 172-184.). The presence of oxygenated and nitrated-derivatives PAHs is also a matter of concern in recent years (Cousin Cachot 2014COUSIN X CACHOT J. 2014. PAHs and fish exposure monitoring and adverse effects from molecular to individual level. Environ Sci Pollut Res 21: 13685-13688., Wincent et al. 2015WINCENT E, JÖNSSON ME, BOTTAI M, LUNDSTEDT S DREIJ K. 2015. Aryl hydrocarbon receptor activation and developmental toxicity in zebrafish in response to soil extracts containing unsubstituted and oxygenated PAHs. Environ Sci Technol 49: 3869-3877.).

Paradoxically, that most of the information regarding negative biological effects is available for parental rather than alkylated PAHs (Fallahtafti et al. 2012FALLAHTAFTI S, RANTANEN T, BROWN RS, SNIECKUS V HODSON PV. 2012. Toxicity of hydroxylated alkyl-phenanthrenes to the early life stages of Japanesemedaka (Oryzias latipes). Aquatic Toxicology 106: 56-64.). For instance, both the US-EPA and the International Agency for Research on Cancer (IARC 2010IARC. 2010. Some non-heterocyclic polycyclic aromatic hydrocarbons and some related exposures. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, p. 773.) include only parental compounds in the list of PAHs that may pose a carcinogenic risk to humans (Table I). Humans are exposed to PAHs through inhalation, dermatological contact, or consumption of contaminated food. The PAHs represent high risks to human health due to their lipophilic characteristic (Hamidi et al. 2016HAMIDI EN, HAJEB P, SELAMAT J RAZIS AFA. 2016. Polycyclic Aromatic Hydrocarbons (PAHs) and their Bioaccessibility in Meat: A Tool for Assessing Human Cancer Risk. APJCP 17: 15-23.). These lipophilic compounds are easily bioaccumulated in organisms and biomagnified through the marine food chain, reflecting seafood contamination, including seaweed (Figure 1) (Fogaça et al. 2018FOGAÇA FHS ET AL. 2018. Polycyclic aromatic hydrocarbons bioaccessibility in seafood: Culinary practices effects on dietary exposure. Environ Res 164: 65-172., Nisha et al. 2019NISHA LLJL, ARTHANAREESWARAN G, POONGUZHALI TV, MOHAN TA VALENTINA J. 2019. Phycoremediation of hydrocarbon using two marine seaweeds from the Bay of Bengal coast of India. Desalination Water Treat 156: 378-386.). To control the health risk due to consumption of contaminated seafood, the ‘limit of concern’ (LOC) is usually considered. The LOC represents the maximum concentration of carcinogenic PAHs allowed in the seafood in a risk assessment protocol, which also considers other aspects, like consumption habits, time of exposure, and population age (e.g., Wenzl Zelinkova 2019WENZL T ZELINKOVA Z. 2019. Polycyclic Aromatic Hydrocarbons in Food and Feed, in: Melton L, Shahidi F Varelis P (Eds), Encyclopedia of Food Chemistry. Academic Press, Oxford, p. 455-469.).

Figure 1
Oil spill impacts in different types of aquatic organisms based on where they live, feed, and breed and how mobile they are.
Table I
PAH classification.

One approach to defining de LOC of PAHs in seafood is the consideration of toxic equivalencies (TEQ) of individual PAHs (only 4 to 6 ring-PAHs) to benzo(a)pyrene, as adopted by NOAA/USA after the Gulf of Mexico Deep-Water Horizon oil spill in 2010 (Ylitalo et al. 2012YLITALO GM ET AL. 2012. Federal seafood safety response to the Deepwater Horizon oil spill. PNAS 109: 20274-20279.). This was the same approach adopted by the Brazilian Health Regulatory Agency (ANVISA) after the mysterious oil spill in NE Brazil by launching a Technical Note (27/2019/SEI/GGALI/DIRE2/ANVISA). In this note, it was considered the consumption of 180 g of fish per day and 60 g of crustaceans and molluscs per day, five-year of exposure, and the benzo(a)pyrene (BaP) equivalent, which means the weighted sum for 8 PAHs (benzo(a)anthracene, chrysene, benzo(a)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, dibenzo(a,h)anthracene, indene(1,2,3-cd)pyrene and benzo(g,h,i)perylene). The calculated LOC in BaP-toxic equivalents was 6 µg/kg (or ng/g) for fish and 18 µg/kg (or ng/g) for crustaceans and molluscs.

Another example to establish LOC for PAHs is the legislation adopted in the European community for regular consumption of fisheries that might be chronically contaminated, which defines the maximum concentration (i.e., the LOC) of 5.0 µg/kg for benzo(a)pyrene or 30.0 µg/kg for the sum of benzo(a)pyrene, benzo(a)anthracene, benzo(b)fluoranthene and chrysene (Regulation EC n.835/2011). It is noteworthy that this regulation is an update of an earlier version (Regulation EC n. 1881/2006), excluding threshold values for edible fishes and crustaceans based on the assumption that these animals can metabolize PAHs and thus have a low tendency to accumulate them in muscle tissues.

Effect of PAH bioaccumulation reported in Brazilian aquatic organisms

Several researchers have focused on identifying and quantifying the environment PAHs to evaluate their effects on aquatic organisms and the ecological disturbances in marine wildlife (Maranho et al. 2006MARANHO LT, PREUSSLER KH, MUÑIZ GIB KUNIYOSHI YS. 2006. Efeitos da poluição por petróleo na estrutura da folha de Podocarpus lambertii Klotzsch ex Endl., Podocarpaceae. Acta Bot Bras 20: 615-624., Froehner et al. 2011FROEHNER S, MACENO M MACHADO KS. 2011. Predicting bioaccumulation of PAHs in the trophic chain in the estuary region of Paranagua, Brazil. Environ Monit Assess 174: 135-145., Craveiro et al. 2021CRAVEIRO N, ALVES RVA, SILVA JM, VASCOCELOS E, ALVES-JUNIOR FA FILHO JSR. 2021. Immediate effects of the 2019 oil spill on the macrobenthic fauna associated with macroalgae on the tropical coast of Brazil. Mar Pollut Bull 165: 112107.). PAH can bioaccumulate in different animal groups through biomagnification, even over long distances, being transported by sea currents and wind actions, reaching vulnerable ecosystems (Szewczyk 2006SZEWCZYK SBO. 2006. Processos envolvidos em um derramamento de óleo no mar. In Seminário e Workshop em Engenharia Oceânica (SEMENGO).). Due to its persistence in the environment, studies show that even months and years after an oil spill at sea, it is still possible to find PAH residues in animal tissues, water, and sediment (Silva et al. 2009SILVA CA, RIBEIRO CAO, KATSUMITI A, ARAÚJO, MLP, ZANDONA EM, SILVA GPC, MASCHIO J, ROCHE H ASSIS, HCS. 2009. Evalution of waterborne exposure to oil spill 5 years an accident in Southern Brazil. Ecotoxicol Environ Saf 72: 400-409., Souza-Bastos Freire 2011SOUZA-BASTOS LR FREIRE CA. 2011. Osmorregulation of the resident estuarine fish Atherinella brasiliensis was still affected by an oil spill (Vicuña tanker, Paranaguá Bay, Brazil), 7 months after the accident. Sci Total Environ 409: 1229-1234.). In a short time, there was a reduction in the richness, diversity, and uniformity of the seaweed Jania capillacea due to its oil coating, on Paiva beach (Pernambuco state, North-eastern Brazil), however, after two months its characteristics soon returned to the original state (Craveiro et al. 2021CRAVEIRO N, ALVES RVA, SILVA JM, VASCOCELOS E, ALVES-JUNIOR FA FILHO JSR. 2021. Immediate effects of the 2019 oil spill on the macrobenthic fauna associated with macroalgae on the tropical coast of Brazil. Mar Pollut Bull 165: 112107.).

The impact of the oil spill causes different levels of PAH bioaccumulation in filtering and high trophic level aquatic organisms (Figure 1) (Euzebio et al. 2019, Instituto Terra-Mar 2019INSTITUTO TERRA-MAR. 2019. Derramamento de petróleo na costa Nordestina. Crime e Tragédia Ambiental. Instituto Terra-Mar, 16 p. Available in: https://issuu.com/instituto.terramar.ce/docs/petroleo_crime_tragedia.
https://issuu.com/instituto.terramar.ce/...
). Filtering organisms, such as molluscs, can absorb high levels of contaminants in their tissues (Wilson et al. 1992WILSON EA, POWELL EN, TAYLOR WRJ, PRESLEY BJ BROOKS JM. 1992. Spatial and temporal distributions of contaminant body burden and disease in Gulf of Mexico oyster populations: The role of local and large-scale climatic controls. Helgol Meeresunters 46: 201-235., Araújo et al. 2016ARAÚJO CFS, LOPES MV, VASQUEZ MR, PORCINO TS, RIBEIRO ASV, RODRIGUES JLG, OLIVEIRA SSP MENEZES-FILHO JA. 2016. Cadmium and lead in seafood from the Aratu Bay, Brazil and the human health risk assessment. Environ Monit Assess 188: 259., Shi et al. 2016SHI J, ZHENG J-S, WONG M-H, LIANG H, LI Y, WU Y, LI P LIU W. 2016. Health risks polycyclic aromatic hydrocarbons via fish consumption in Haimen bay (China), downstream of an e-waste recycling site (Guiyu). Environ Res 147: 233240.). Fish and crustaceans have shown a low capacity to bioaccumulate PAH (Graham et al. 2015GRAHAM L, HALE C, MAUNG-DOUGLASS E, SEMPIER S, SWANN L WILSON M. 2015. Oil Spill Science: The Deepwater Horizon Oil Spill’s Impact on Gulf Seafood. MASGP-15-014., Lourenço et al. 2018LOURENÇO RA ET AL. 2018. Bioaccumulation Study of Produced Water Discharges from Southeastern Brazilian Offshore Petroleum Industry Using Feral Fishes. Arch Environ Contam Toxicol 74: 461-470.).

Since the feeding habits influence PAH bioaccumulation, carnivorous fish shall accumulate higher levels of these compounds. However, Soares-Gomes et al. (2010)SOARES-GOMES A, NEVES RL, AUCÉLIO R, VAN DER VEN PH, PITOMBO FB, MENDES CLT ZIOLLI RL. 2010. Changes and variations of polyccyclic aromatic hydrocarbon concentrations in fish, barnacles and crabs following an oil in a mangrove of Guanabara Bay, Southeast Brazil. Mar Pollut Bull 60: 1359-1363. did not observe a significant difference in the PAH concentrations among the carnivore sea bass (Centropomus parallelus), the detritivore benthic mullet (Mugil liza), and the detractor crustacean mangrove crab (Ucides cordatus). Although the authors observed those barnacle organisms were the most sensitive to the presence of oil in the water, due to their low efficiency in metabolizing such compounds. Elasmobranch, fish, invertebrate, and mammal species are especially vulnerable to exposure to oil spills, as they are species restricted to a depth of less than 100 m (Magris Giarrizo 2020MAGRIS RA GIARRIZZO T. 2020. Mysterious oil spill in the Atlantic Ocean threatens marine biodiversity and local people in Brazil. Mar Pollut Bull 153: 110961.).

Several species exposed to oil have shown physiological abnormalities associated with high concentrations of these compounds in their tissues. Researchers have found that the PAH presence in the environment causes necropsy in fish liver tissues; histological changes in branchial cells, with negative consequences for gas exchange and osmoregulation; growth reduction, among other impacts (Silva et al. 2009SILVA CA, RIBEIRO CAO, KATSUMITI A, ARAÚJO, MLP, ZANDONA EM, SILVA GPC, MASCHIO J, ROCHE H ASSIS, HCS. 2009. Evalution of waterborne exposure to oil spill 5 years an accident in Southern Brazil. Ecotoxicol Environ Saf 72: 400-409., Short 2017SHORT JW. 2017. Advances in Understanding the Fate and Effects of Oil from Accidental Spills in the United States Beginning with the Exxon Valdez. Arch Environ Contam Toxicol 73: 5-11.). The tetra Astyanax spp. showed gill alterations, liver inflammation, and histopathological injuries when exposed to water contaminated by the oil spill in the Pantanal Arroio Saldanha, in Parana state (Silva et al. 2009SILVA CA, RIBEIRO CAO, KATSUMITI A, ARAÚJO, MLP, ZANDONA EM, SILVA GPC, MASCHIO J, ROCHE H ASSIS, HCS. 2009. Evalution of waterborne exposure to oil spill 5 years an accident in Southern Brazil. Ecotoxicol Environ Saf 72: 400-409.). The marine catfish (Genidens genidens) collected from Guanabara Bay, Rio de Janeiro State, showed blood alterations, genotoxic and physiological damage (Freire et al. 2020FREIRE MM, AMORIM LMF, BUCH AC, GONÇALVES AD, SELLA SM, CASSELLA RJ, MOREIRA JC SILVA-FILHO EV. 2020. Polycyclic aromatic hydrocarbons in bays of the Rio de Janeiro state coast, SE - Brazil: Effects on catfishes. Environ Res 181: 108959.). Mangrove crabs, used as bioindicators of environmental health in a port and mangrove region in Brazil Northeastern, showed branchial lesions when collected near the port region, associated with the poor water quality and presence of PAHs (Carvalho Neta et al. 2019CARVALHO NETA RNF, ANDRADE TSOM, OLIVEIRA SRA, JUNIOR ART, CARDOSO WS, SANTOS DMS, BATISTA WS, SERRA IMRS BRITO NM. 2019. Biochemical and morphological responses in Ucides cordatus (Crustacea, Decapoda) as indicators of contamination status in mangroves and port areas from northern Brazil. Environ Sci Pollut Res 2: 15884-15893.).

The PAH presence in the marine environment is not necessarily the result only of oil spills, it is also associated with intense urban-industrial activity (Froehner et al. 2011FROEHNER S, MACENO M MACHADO KS. 2011. Predicting bioaccumulation of PAHs in the trophic chain in the estuary region of Paranagua, Brazil. Environ Monit Assess 174: 135-145.), which intensifies the impacts of contamination on aquatic organisms.

These effects are correlated with highly contaminated areas where aquatic organisms live. Mussels (Perna perna) collected in an area with intense urban-industrial activity showed high PAH concentration in their tissues compared to those further away from the urban area (Santiago et al. 2016SANTIAGO IU, MOLISANI MM, NUDI AH, SCOFIELD AL, WAGENER ALR LIMAVERDE FILHO AM. 2016. Hydrocarbons and trace metals in mussels in the Macaé coast: Preliminary assessment for a coastal zone under influence of offshore oil field exploration in southeastern Brazil. Mar Pollut Bull 103: 349-353.). Camargo et al. (2017)CAMARGO MZ, SANDRINI-NETO L, CARREIRA RS CAMARGO MG. 2017. Effects of hydrocarbon pollution in the structure of macrobenthic assemblages from two large estuaries in Brazil. Mar Pollut Bull 125: 66-76. have shown that the presence of PAHs was a cause of alteration in the structure of the benthic macrofauna in Guanabara and Laranjeira bays (Rio de Janeiro and Paraná state, respectively).

The presence of PAH in the marine environment will not always be reflected in acute adverse effects on aquatic organisms, especially those that metabolize and excrete such compounds (Bandowe et al. 2014BANDOWE BAM, BIGALKE M, BOAMAH L, NYARKO E, SAALIA FK WILCKE W. 2014. Polycyclic aromatic compounds (PAHs and oxygenated PAHs) and trace metals in fish species from Ghana (West Africa): Bioaccumulation and health risk assessment. Environ Int 65: 135-146., Lourenço et al. 2018LOURENÇO RA ET AL. 2018. Bioaccumulation Study of Produced Water Discharges from Southeastern Brazilian Offshore Petroleum Industry Using Feral Fishes. Arch Environ Contam Toxicol 74: 461-470.). For instance, Lourenço et al. (2018)LOURENÇO RA ET AL. 2018. Bioaccumulation Study of Produced Water Discharges from Southeastern Brazilian Offshore Petroleum Industry Using Feral Fishes. Arch Environ Contam Toxicol 74: 461-470. evaluated the presence of PAH and trace elements in Coranx crysos and Tylosurus acus tissues and demonstrated that their presence characterizes the production of water from oil and gas platforms in the Campos Basin (Rio de Janeiro state) as minimally polluted.

Another effect observed in aquatic organisms exposed to PAH is related to the behaviour of these species. Tambaqui fish (Colossoma macropomum) showed changes such as reduction in swimming activity and predatory behaviour, associated with the lamellar and gill fusion, when exposed to insoluble crude oil fractions from an Oil Company located on the Urucu River, in the state of Amazonas (Kochhann et al. 2015KOCHHANN D, JARDIM MM, DOMINGUES FXV VAL AL. 2015. Biochemical and behavioral responses of the Amazonian fish Colossoma macropomum to crude oil: The effect of oil layer on water surface. Ecotoxicol Environ Saf 111: 32-41.). The presence of oil in the water affected the fish breathing and the water-air interface (Magris Giarrizzo 2020).

PAH consumption and health risk

The impact of the oil spill has irremediable effects on many aquatic species (Baršienė et al. 2008BARŠIENĖ J, ANDREIKĖNAITĖ L, GARNAGA G RYBAKOVAS A. 2008. Genotoxic and cytotoxic effects in the bivalve mollusks Macoma balthica and Mytilus edulis from the Baltic Sea. EKOLOGIJA 54: 44-50., Bado-Nilles et al. 2009BADO-NILLES A, QUENTEL C, THOMAS-GUYON H FLOCH SL. 2009. Effects of two oils and 16 pure polycyclic aromatic hydrocarbons on plasmatic immune parameters in the European sea bass, Dicentrarchus labrax (Linné). Toxicol Vitro 23: 235-241., Chen Denison 2011CHEN J DENISON MS. 2011. The Deepwater Horizon oil spill: environmental fate of the oil and the toxicological effects on marine organisms. JYI 21: 84-95., Yuewen Adzigbl 2018YUEWEN D ADZIGBL L. 2018. Assessing the Impact of Oil Spills on Marine Organisms. J Oceanogr Mar Res 6: 2572-3103.). In addition, the presence of oil slicks or their fractions makes these organisms vulnerable, affecting the entire food web, including humans, since the consumption of oil-contaminated seafood represents a risk to human health.

The 2 to 6 ring PAHs are a concern for short and medium-term food safety (Yender et al. 2002YENDER R, MICHEL J LORD C. 2002. Managing seafood safety after an oil spill. US Department of Commerce, National Oceanic and Atmospheric Administration, National Ocean Service, Office of Response and Restoration, Seattle, p. 72.). Although the toxicity potential of PAHs is recognized, to assess whether there is a risk in consuming seafood in oil-contaminated areas, a level of concern must be established (Gohlke et al. 2011GOHLKE JM, DOKE D, TIPRE M, LEADER M FITZGERALD T. 2011. A Review of Seafood Safety after the Deepwater Horizon Blowout. Environ. Health Perspect 119: 1062-1069.). The Food and Drug Administration (FDA) provides guidelines for the types and amount of seafood that consumers can eat, after the Gulf of Mexico oil spill (Graham et al. 2015GRAHAM L, HALE C, MAUNG-DOUGLASS E, SEMPIER S, SWANN L WILSON M. 2015. Oil Spill Science: The Deepwater Horizon Oil Spill’s Impact on Gulf Seafood. MASGP-15-014.). Even in the USA, scientists are concerned about allowable intake doses combined with food consumption data or consumption scenarios (Scholl et al. 2012SCHOLL G, HUYBRECHTS I, HUMBLET MF, SCIPPO ML, DE PAUW E, EPPE G SAEGERMAN C. 2012. Risk assessment for furan contamination through the food chain in Belgian children. Food Addit Contam Part A 29: 1219-1229.) to determine the risk associated. This is because some ethnic groups have a higher consumption of seafood per kg of body weight. In this case, these thresholds, as well as the risk assessment of seafood intake in general, are questionable (Marques et al. 2011MARQUES A, LOURENÇO HM, NUNES ML, ROSEIRO C, SANTOS C, BARRANCO A, RAINIERI S, LANGERHOLC T CENCIC A. 2011. New tools to assess toxicity, bioaccessibility and uptake of chemical contaminants in meat and seafood. Food Res Int 44: 510-522.).

The PAH intake of seafood was estimated to be 15.3 ng / kg body weight per day for Koreans. Furthermore, high molecular weight and carcinogenic PAH profile have been observed in bivalves molluscs, although these food products only account for 29% of total PAHs consumption (Moon et al. 2010MOON H-B, KIM H-S, CHOI M CHOI H-G. 2010. Intake and Potential Health Risk of Polycyclic Aromatic Hydrocarbons Associated with Seafood Consumption in Korea from 2005 to 2007. Arch Environ Contam Toxicol 58: 214-221.).

The PAH concentrations of 0.04 to 1.17 ng/kg body weight per day found in Sardina pilchardus and Solea solea collected at Catatania by Ferrante et al. (2018)FERRANTE M, ZANGHI G, COPAT C, GRASSO A, FIORE M, SIGNORELLI SS, ZUCCARELLO P CONTI GO. 2018. PAHs in seafood from the Mediterranean Sea: An exposure risk assessment. Food Chem Toxicol 115: 385-390., did not represent a risk to human consumption, as such concentrations are below the defined maximum limit by European Food Safety Authority (EFSA). Although low molecular weight PAHs are not classified as carcinogens, their chronic ingestion can cause negative impacts on human health (Rotkin-Ellman et al. 2012ROTKIN-ELLMAN M, WONG KK SOLOMON GM. 2012. Seafood Contamination after the BP Gulf Oil Spill and Risks to Vulnerable Populations: A Critique of the FDA Risk Assessment. Environ. Health Perspect 120: 157-161.).

It seems that the concern about the concentration of PAHs in aquatic organisms for human health is due to the culture of consumption of such proteins. For the adult population of Kuwait, the estimated mean daily consumption of seafood was 66.4 g/day, lower than that set by the US EPA (142.2 g/day) (Alomirah et al. 2009ALOMIRAH H, AL-ZENKI S, HUHSAIN A, AHMED N, AL-RASHDAN A, GEVAO B SAWAYA W. 2009. Dietary exposure to polycyclic aromatic hydrocarbons from commercially important seafood of the Arabian Gulf. J Food Agric Environ 7: 9-15.). These authors observed that even the high presence of low molecular weight (LMW) PAH in fish consumed by the Kuwait population does not pose a health risk. The high concentration of naphthalene and phenanthrene in fish also poses no risk to the Canadian population, even with an average daily intake of PAH from seafood was 1.097 ng/day for men and 1.051 ng/day for women (Ohiozebau et al. 2017OHIOZEBAU E, TENDLER B, CODLING G, KELLY E, GIESY JP JONES PD. 2017. Potential health risks posed by polycyclic aromatic hydrocarbons in muscle tissues of fishes from the Athabasca and Slave Rivers, Canada. Environ Geochem Health 39: 139-160.).

Recently, in Brazil, Massone et al. (2021)MASSONE CG, SANTOS AA, FERREIRA PG CARREIRA RS. 2021. A baseline evaluation of PAH body burden in sardines from the southern Brazilian shelf. Mar Pollut Bull 163: 111949. observed levels of some PAHs with carcinogenic potential in sardine muscles (Sardinella brasiliensis). The authors state that the presence of B(a)P, whose concentration was higher than 6 μg/kg in 4% of their samples, does not represent a risk to the consumption of this fish. However, it is important to continue monitoring Brazilian fish to ensure food safety.

The PAH profile in fish muscles is generally characterized by low molecular weight compounds, most likely due to the difficulty of organisms to bioaccumulate high molecular weight PAH (Ni Guo 2013NI H-G GUO J-Y. 2013. Parent and halogenated polycyclic aromatic hydrocarbons in Seafood from south China and implications for human exposure. J Agric Food Chem 61: 2013-2018., Akhbarizadeh et al. 2019AKHBARIZADEH R, MOORE F KESHAVARZI B. 2019. Polycyclic aromatic hydrocarbons and potentially toxic elements in seafood from the Persian Gulf: presence, trophic transfer, and chronic intake risk assessment. Environ Geochem Health 41: 2803-2820.). The concentration of PAH in fish muscles also varies according to their trophic level, due to the interaction between PAH and the lipid content of different species (Recabarren-Villalón et al. 2021RECABARREN-VILLALÓN T, RONDA AC, OLIVA AL, CAZORLA AL, MARCOVECCHIO JE ARIAS AH. 2021. Seasonal distribution pattern and bioaccumulation of Polycyclic aromatic hydrocarbons (PAHs) in four bioindicator coastal fishes of Argentina. Environ Pollut 291: 118125.). Furthermore, intrinsic (sexual maturation stage, age, body weight) and extrinsic factors (food web position, lifestyle, food availability) contribute to the differences in the concentration of these compounds (Mahugija Njale 2018MAHUGIJA JAM NJALE E. 2018. Levels of polycyclic aromatic hydrocarbons (PAHs) in smoked and sun-dried fish samples from areas in Lake Victoria in Mwanza, Tanzania. J Food Compost Anal 73: 39-46., Habibullah-Al-Mamun et al. 2019HABIBULLAH-AL-MAMUN MD, AHMED MDK, ISLAM MDS, TOKUMURA M MASUNAGA S. 2019. Distribuition of polycyclic aromatic hydrocarbons (PAHs) in commonly consumed seafood from coastal areas of Bangladesh and associated human health implications. Environ Geochem Health 41: 1105-1121.).

Most studies on the concern about the consumption of contaminated fish, such as Oliveira et al. (2020)OLIVEIRA M, PORTELLA CDG, RAMALHOSA MJ, DELERUE-MATOS C, SANT’ANA LS MORAIS S. 2020. Polycyclic aromatic hydrocarbons in wild and farmed whitemouth croaker and meagre from different Atlantic Ocean fishing areas: Concentrations and human health risk assessment. Food Chem Toxicol 146: 111797., highlight the concentration and profile of PAH in fish muscles. These authors observed that the Portuguese population is more vulnerable to the carcinogenicity of PAHs when they feed on whitemouth Argyrosomus regius from captivity, due to the high presence of high molecular weight (HMW) PAHs in their samples.

To enhance the taste and improve the appearance, fish are often consumed after undergoing some culinary processing. However, its nutritional content can change according to the addition of spices and/or thermal processing. Thus boiling, cooking, grilling, and roasting, among others, can reduce the concentration of contaminants in food matrices, making them safer (Mi et al. 2017MI X-B, SU Y, BAO L-J, TAO S ZENG EY. 2017. Significance of Cooking Oil to Bioaccessibility of Dichlorodiphenyltrichloroethanes (DDTs) and Polybrominated Diphenyl Ethers (PBDEs) in Raw and Cooked Fish: Implications for Human Health Risk. J Agric Food Chem 65: 3268-3275., Girard et al. 2018GIRARD C, CHARETTE T, LECLERC M, SHAPIRO BK AMYOT M. 2018. Cooking and co-ingested polyphenols reduce in vitro methylmercury bioaccessibility from fish and may alter exposure in humans. Sci Total Environ 616: 863-874.).

Depending on the culinary treatment, PAHs may also tend to aggregate to lipid particles in the gastrointestinal tract, due to their lipophilic characteristics, making them more bioaccessible during the digestive process (Harris et al. 2013HARRIS KL, BANKS LD, MANTEY JA, HUDERSON AC RAMESH A. 2013. Bioaccessibility of polycyclic aromatic hydrocarbons: relevance to toxicity and carcinogenesis. Drug Metab Toxicol 9: 11.). The EC Regulation number 1881/2006 and subsequent amendments (EC Regulation No. 835/2011 and 1327/2014) set the maximum allowable concentration of B(a)P for non-smoked fish (2 μg/kg wet weight), for crustaceans and cephalopod molluscs not smoked (5 μg/kg wet weight) and for not smoked bivalve molluscs (10 μg/kg wet weight) (Ferrante et al. 2018FERRANTE M, ZANGHI G, COPAT C, GRASSO A, FIORE M, SIGNORELLI SS, ZUCCARELLO P CONTI GO. 2018. PAHs in seafood from the Mediterranean Sea: An exposure risk assessment. Food Chem Toxicol 115: 385-390.).

The PAH dietary daily intake (DDI) in smoked fish for Nigerians was estimated to Clarias gariepinus (0.039 mg/day), Tilapia zilli (0.052 mg/day), Ethmalosa fimbriata (0.038 mg/day) and Scomber scombrus (0.195 mg/day). A DDI value for the total carcinogenic PAHs (∑CPAHs) was highest for E. fimbriata, indicating a greater risk of consumption of this species compared to the others (Tongo et al. 2017TONGO I, OGBEIDE O EZEMONYE L. 2017. Human health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in smoked fish species from markets in Southern NigeriaIsioma. Toxicol Rep 4: 55-61.). It is evident, therefore, that cooking techniques using burning can make PAH bioavailable to the human body through seafood consumption.

In countries whose fish consumption represents the main source of animal protein, the risk analysis for human health is extremely important to ensure food safety. The average consumption of fish in the world is 20.5 kg/per capita, however, in Brazil, such consumption depends on the region. In the Amazonian region, for example, they consume about 50 kg/per capita/year of seafood, about five times higher than the Brazilian average and almost three times higher than the world consumption (Gervásio 2019GERVÁSIO EW. 2019. Piscicultura Análise da Conjuntura. SEAB - Secretaria de Estado da Agricultura e do Abastecimento. Paraná, Br. Disponível em: https://www.agricultura.pr.gov.br/sites/default/arquivos_restritos/files/documento/2021-08/pesca_aquicultura_2019_v1.pdf.
https://www.agricultura.pr.gov.br/sites/...
, FAO 2020FAO - FOOD AND AGRICULTURE ORGANIZATION. 2020. The State of World Fisheries and Aquaculture: Sustainability in action. Roma, 250 p.).

Although the vast majority of studies indicate that there is no risk in consuming seafood with some levels of PAH, it is important to continue monitoring these compounds. Fish consumption contributes 13.1% and 8.1% of LMW and HMW PAH, respectively, being the third category of foods that provide the most contaminants for humans through their daily consumption (Yu et al. 2015YU Z-L, LI Q, WANG H, WANG X, REN A TAO S. 2015. Risk of human exposure to polycyclic aromatic hydrocarbons: A case study in Beijing, China. Environ Pollut 205: 70-77.).

Yu et al. (2012)YU Y-X, CHEN L, YANG D, PANG Y-P, ZHANG S-H, CHANG X-Y, YU Z-Q, WU M-H FU J-M. 2012. Polycyclic aromatic hydrocarbons in animal-based foods from Shanghai: bioaccessibility and dietary exposure. Food Addit Contam Part A 29:1465-1474. observed that consumption in large quantities of clam Mactra chinensis e snail Bellamya poses a risk to human health due to the high potency equivalent concentrations and PAH values could pose a carcinogenic risk.

The presence of PAH in the edible tissues of octopus Octopus vulgaris, Octopus maya, and Eledone cirrhosa do not represent a health risk, with overall LMW PAH concentrations being 86–92% of the total (Oliveira et al. 2018OLIVEIRA M, GOMES F, TORRINHA A, RAMALHOSA MJ, DELERUE-MATOS C MORAIS S. 2018. Commercial octopus species from different geographical origins: Levels of polycyclic aromatic hydrocarbons and potential health risks for consumers. Food Chem Toxicol 121: 272-282.). The concentration of non-carcinogenic PAH can also reveal a picture of risk to human health and aquatic organisms (Nasher et al. 2016NASHER E, HENG LY, ZAKARIA Z SURIF S. 2016. Health risk assessment of polycyclic aromatic hydrocarbons through aquaculture fish consumption, Malaysia. Environ. Forensics 17: 97-116.) because it represents a chronic exposure of consumers and bioaccumulation of these compounds in the environment.

Fish consumption is generally encouraged due to the benefits associated with its lipid composition, omega-3 and omega-6, and other nutrients; on the other hand, depending on the fishing/farming location, these organisms may be more vulnerable to contaminants, and consuming them may pose a health risk (Oliveira et al. 2020OLIVEIRA M, PORTELLA CDG, RAMALHOSA MJ, DELERUE-MATOS C, SANT’ANA LS MORAIS S. 2020. Polycyclic aromatic hydrocarbons in wild and farmed whitemouth croaker and meagre from different Atlantic Ocean fishing areas: Concentrations and human health risk assessment. Food Chem Toxicol 146: 111797., Ju et al. 2022JU Y-R, CHEN C-F, WANG M-H, CHEN C-W DONG C-D. 2022. Assessment of polycyclic aromatic hydrocarbons in seafood collected from coastal aquaculture ponds in Taiwan and human health risk assessment. J Hazard Mater 421: 126708.). Thus, the risk assessment for the consumption of fish associated with sites of intense anthropogenic activity and accidents with oil spills must continue.

In addition, there are new tools to assess the bioavailable amount of contaminants in seafood. Bioaccessibility refers to the portion of the food that is released after digestion in the gastrointestinal tract (Saura-Calixto et al. 2007SAURA-CALIXTO F, SERRANO I GONI I. 2007. Intake and bioaccessibility of total polyphenols in whole diet. Food Chem 101: 492-501.), reaching the systemic circulation and becoming bioavailable. Quantifying the bioaccessibility of these compounds would make risk analysis more realistic (Afonso et al. 2015AFONSO C, COSTA S, CARDOSO C, BANDARRA N, BATISTA I, COELHO I, CASTANHEIRA I NUNES ML. 2015. Evaluation of the risk/benefit associated to the consumption of raw and cooked farmed meagre based on the bioaccessibility of selenium, eicosapentaenoic acid and docosahexaenoic acid, total mercury, and methylmercury determined by an in vitro digestion model. Food Chem 170: 249-256.). Bioaccessibility reduced the PAHs concentration in marine and freshwater fish muscles. This shows that the level of concern about the consumption of contaminated seafood is overestimated. Besides, the LMW PAHs are more bioaccessible for the gastrointestinal tract than those HMW PAHs, because of the hydrophobic characteristics (Wang et al. 2010WANG H-S, MAN Y-B, WU F-Y, ZHAO Y-G, WONG CKC WONG M-H. 2010. Oral Bioaccessibility of Polycyclic Aromatic Hydrocarbons (PAHs) Through Fish Consumption, Based on an in Vitro Digestion Model. J. Agric. Food Chem. 58: 11517-11524.).

Recently, studies have shown that bioaccessibility has reduced the level of daily intake of PAHs in samples of mussels (Fogaça et al. 2018FOGAÇA FHS ET AL. 2018. Polycyclic aromatic hydrocarbons bioaccessibility in seafood: Culinary practices effects on dietary exposure. Environ Res 164: 65-172.) and oysters (Hong et al. 2016HONG W-J, JIA H, LI Y-F, SUN Y, LIU X WANG L. 2016. Polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs in the coastal seawater, surface sediment and oyster from Dalian, Northeast China. Ecotoxicol Environ Saf 128: 11-20.). Unfortunately, in Brazil, there are still no studies on the PAH bioaccessibility in seafood. And the results of the PAH bioaccumulation analyses in samples collected after the oil spill in NE Brazil are still in the processing and publication phase. Therefore, there will be only one scenario of the impact of the accident in the coming years.

CONCLUSIONS

In the year that Ocean Decade begins, it is necessary a greater scientific and civil demand from the government authorities in assigning plausible punishments to those responsible for the causes of oil spills. In addition, the literature lacks further scientific research on the chronic effects of exposure to spots by aquatic organisms, especially those targeted by fishing and aquaculture, whether or not the product is validated for human consumption.

ACKNOWLEDGMENTS

This work was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES, Grant 26/2019, Program Capes Entre-Mares 0009/2020).

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Publication Dates

  • Publication in this collection
    17 June 2022
  • Date of issue
    2022

History

  • Received
    31 Aug 2021
  • Accepted
    1 Feb 2022
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