Acessibilidade / Reportar erro

Oil Spill Disaster in Southwest Atlantic Coast: an Evaluation of Short-Term Effects on Coral Reef Benthic Assemblages

Abstract

Oil pollution has significantly contributed to coral reef decline in the last five decades and a major oil spill reached Brazilian tropical coast in August 2019. Here, we report the first evidence of direct crude oil contact from that spill on reef coral species, and evaluate the effects of this disaster on coral vitality and benthic assemblage structure on the largest coastal marine protected area (MPA Costa dos Corais) in Brazil. We compared benthic cover in reefs with and without oil and monitored Siderastrea stellata colonies 90 days after oil contact. Oil stains between 0.5 and 150 cm were found in two of the 17 reef sites investigated. Multivariate analyses did not detect significant differences between oiled and non-oiled reefs and there was no evidence of S. stellata health deterioration. These results indicate minimal acute effects on coral vitality and intertidal reef benthic assemblage structure. Future studies should investigate oil effects on specific aspects of coral biology as growth, reproduction, bleaching susceptibility and metagenomics which can deteriorate over longer time frames, and we recommend long-term coral reef monitoring to support a robust assessment and mitigation of chronic oil impacts.

Key words
Siderastrea stellata; Acute effects; Costa dos Corais; impact; pollution

INTRODUCTION

Oil pollution has been a major environmental threat on the oceans in the last decades, with acute and chronic effects that persist over long periods and which contribute to ecosystem deterioration (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.). Oil pollution has several sources, some of worst being massive oil blowouts, pipeline ruptures, and explosions at storage facilities (Burgherr 2007BURGHERR P. 2007. In-depth analysis of accidental oil spills from tankers in the context of global spill trends from all sources. J of Hazard Mater 140: 245-256.). Although the number of spills and the quantity of spilled oil globally decreased between 1970 and 2000, more recent disasters have impacted sensitive reef areas with uncertain long-term consequences (Seveso et al. 2021SEVESO D, LOUIS YD, MONTANO S, GALLI P & SALIU F. 2021. The Mauritius Oil Spill: What’s Next? Pollutants 1: 18-28. https:// doi.org/10.3390/pollutants1010003.
https://doi.org/.https://doi.org/10.3390...
). For example, while some studies have evaluated oil effects in the lab (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.), little is known about oil effects on key species and ecosystem processes.

Oil spills are among the drivers that contribute to rapid decline of coral reefs worldwide (Loya & Rinkevich 1980LOYA Y & RINKEVICH B. 1980. Effects of oil pollution on coral reef communities. Mar Ecol Prog Ser 3: 167-180., Hughes et al. 2017HUGHES TP ET AL. 2017. Coral reefs in the Anthropocene. Nature 546: 82-90.). Oil impacts on reef species depend on quantity and density of the oil, as well as the exposure time and biological characteristics (Santos et al. 2015SANTOS HF ET AL. 2015. Impact of oil spills on coral reefs can be reduced by bioremediation using probiotic microbiota. Sci Rep 5: 18268. https://doi.org/10.1038/srep18268.
https://doi.org/.https://doi.org/10.1038...
). Due to coral’s importance for reef structure and trophic interactions, acute effects of oil on corals could cause an ecosystem collapse (Loya & Rinkevich 1980LOYA Y & RINKEVICH B. 1980. Effects of oil pollution on coral reef communities. Mar Ecol Prog Ser 3: 167-180.), such as the extensive mortality of shallow subtidal reef corals and a rapid decrease in species diversity (Jackson et al. 1989JACKSON JBC ET AL. 1989. Ecological effects of a major oil spill on Panamanian coastal marine communities. Science 243: 37-44., Guzmán et al. 1991GUZMÁN HM, JACKSON JBC & WEIL E. 1991. Short-term ecological consequences of a major oil spill on Panamanian subtidal reef corals. Coral Reefs 10: 1-12.).

In late August 2019 crude oil of unknown origins began to wash up on the Brazilian coastline (Escobar 2020ESCOBAR H. 2020. Mysterious oil spill threatens marine biodiversity haven in Brazil. Science. https://doi.org/10.1126/science.aba1003.
https://doi.org/10.1126/science.aba1003...
, Magris & Giarrizzo 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.). Five months after the first report at least 5,000 tons had been found along > 3,000 km of coast in 11 states, including more than 980 localities. This made the oil spill the worst environmental disaster - in terms of oil quantity and geographic range - ever recorded at the South Atlantic Ocean. The crude oil from the spill reached at least 57 Marine Protected Areas (MPA), including iconic beaches, mangroves, seagrass, rhodolith beds and coral reefs (Sissini et al. 2020SISSINI MN ET AL. 2020. Brazil oil spill response: Protect rhodolith beds. Science 367: 156., Soares et al. 2020aSOARES MO ET AL. 2020a. Oil spill in South Atlantic (Brazil): Environmental and governmental disaster. Mar Policy 115: 103879.). The Brazilian reefs are unique representatives of the largest biodiversity hot spot in the southern Atlantic Ocean, harbouring relic coral species with highest levels of endemism (Leão et al. 2003LEÃO ZMAN, KIKUCHI RKP & TESTA V. 2003. Corals and coral reefs of Brazil. In: CORTÉS J (Ed), Latin America corals reefs, Amsterdam: Elsevier, p. 9-52.). However, no studies have assessed short-term effects of the oil spill on corals of Brazil and the magnitude of the impact on coral reefs remains largely unknown (Miranda et al. 2020aMIRANDA RJ, ALMEIDA ECG, PINTO TK, SAMPAIO CLS, PEREIRA PHC, NUNES JACC & LADLE RJ. 2020a. Oil spill disaster in Brazil: impact assessment neglecting unique coral reefs. Science 366: 6466. sciencemag.org/content/366/6466/672/tab-eletters.).

In the present study, we report on direct interactions between crude oil and reef coral species in the largest coastal marine protected area (MPA) in Brazil (the Environmental Protected Area of Costa dos Corais - APACC). We evaluate whether crude oil negatively affected the benthic assemblage structure and coral species vitality in the short-term after oil contact. To achieve this, we tested whether: (1) reef sites where crude oil was found have different structure of benthic assemblages compared with non-oiled sites, and (2) direct contact with oil causes a decrease in vitality of coral species, such as bleaching, tecidual necrosis, diseases, corallites number decrease or algae overgrowth.

MATERIALS AND METHODS

Study area

The study was conducted at the marine protected area of Costa dos Corais (hereafter indicated as APACC - Portuguese acronym) the largest multiple use coastal MPA in Brazil. APACC is located along the coast of Pernambuco and Alagoas states, in the northeast of the country in the Southwestern Atlantic (9°01’S, 35°11’W) (Fig. 1). This MPA extends 413,563 hectares and includes 12 municipalities, diverse coral reefs and other important ecological systems (Pereira et al. 2018PEREIRA PHC, MACEDO CH, NUNES JACC, MARANGONI LFB & BIANCHINI A. 2018. Effects of depth on reef fish communities: Insights of a “deep refuge hypothesis” from Southwestern Atlantic reefs. PLoS ONE 13(9): e0203072. https://doi.org/10.1371/journal.pone.0203072.
https://doi.org/.https://doi.org/10.1371...
, Miranda et al. 2020bMIRANDA RJ ET AL. 2020b. Integrating Long Term Ecological Research (LTER) and Marine Protected Area management: challenges and solutions. Oecol Aust 24: 279-300.). The fringing reefs are extensive along the APACC on the inner shelf forming up to three lines parallel to coast (Maida & Ferreira 1997MAIDA M & FERREIRA BP. 1997. Coral reefs of Brazil: An overview. Panamá: Proc 8th Int Coral Reef Symp 1: 263-274., Leão et al. 2003LEÃO ZMAN, KIKUCHI RKP & TESTA V. 2003. Corals and coral reefs of Brazil. In: CORTÉS J (Ed), Latin America corals reefs, Amsterdam: Elsevier, p. 9-52., Ferreira & Maida 2006FERREIRA B & MAIDA M. 2006. Monitoramento dos Recifes de Coral do Brasil. Ministério do Meio Ambiente, Brasília.). These reefs harbor endemic, vulnerable and endangered species, and are one of the “target areas” of National Action Plans for Conservation, a government strategy to improve species conservation, mitigate impacts and encourage sustainable use of natural resources (BRASIL 2016BRASIL. 2016. Portaria ICMBIO n° 19 de 09 de Março de 2016. Aprova o Plano de Ação Nacional para a Conservação dos Ambientes Coralíneos - PAN Corais.). The APACC management plan restricts human activities on these reefs, establishing spatial zoning such as no-take and tourism zones, where only scientific research and controlled tourism visitation are allowed (BRASIL 2013BRASIL. 2013. Portaria ICMBIO n° 144 de 01 de Fevereiro de 2012. Aprova o Plano de Manejo da Área de Proteção Ambiental Costa dos Corais.).

Figure 1
a-b) Map of study area, oil occurrence (beach, estuary and reef sites) and c-d) sampling approach (photo quadrats) in marine protected area Costa dos Corais (APACC), Brazil. O, NO1 and NO2 represent sites of the mensurative experiment to evaluate oil spill effects on benthic assemblages. Oil occurrence data on beaches and estuaries sites from IBAMA (2020)IBAMA - INSTITUTO BRASILEIRO DO MEIO AMBIENTE E DOS RECURSOS NATURAIS. 2020. Manchas de Óleo, Litoral Brasileiro: Localidades atingidas. Available in: http://www.ibama.gov.br/manchasdeoleo-localidades-atingidas. Date Access: 20/06/2021.
http://www.ibama.gov.br/manchasdeoleo-lo...
. Photos: Ricardo J. Miranda.

APACC was one of the Brazilian MPAs most affected by oil spill; an estimated 1,671.83 tons of oiled residues (crude oil plus beach sand and others) were cleaned up by volunteers on the beach, especially in Japaratinga and Maragogi (Fig. 1) municipalities, where 734.32 and 583.43 tons removed respectively, as well as 327.24 tons in Tamandaré/Barreiros, 13.58 in São José da Coroa Grande, 12.34 in Barra de Santo Antônio, 0.75 in Maceió (Ipióca), 0.15 in Passo do Camaragibe and 0.02 in Porto de Pedras (ALAGOAS 2020ALAGOAS. 2020. Reunião Ordinária 300, Conselho Estadual de Proteção Ambiental do Estado de Alagoas – 11 de Fevereiro 2020. Available in: https://www.youtube.com/watch?v=fzhkIFBB2IY Data Access: 10/03/2021.
https://www.youtube.com/watch?v=fzhkIFBB...
, IBAMA 2020IBAMA - INSTITUTO BRASILEIRO DO MEIO AMBIENTE E DOS RECURSOS NATURAIS. 2020. Manchas de Óleo, Litoral Brasileiro: Localidades atingidas. Available in: http://www.ibama.gov.br/manchasdeoleo-localidades-atingidas. Date Access: 20/06/2021.
http://www.ibama.gov.br/manchasdeoleo-lo...
).

Identification of oil stains in the subtidal reefs

To investigate the presence of the oil stains on subtidal reefs (2 to 15m depth), we used snorkel and SCUBA diving surveys in 13 sites determined by the visual observation of three 100 m transects in each site. The surveys were conducted between October and December 2019 in reefs located inside no-take or tourism zones or near to beaches where oil had been reported by local people (Fig. 1).

Evaluation of the oil spill effects on benthic assemblages and coral vitality in the intertidal reefs

We investigated oil presence on the intertidal reefs (4 sites) during low tides by walking. When oil stains were found on the reef, we estimated the range extension and identified direct contacts on coral colonies to monitoring individual short-term effects. To evaluate whether the occurrence of oil stains affected the coral reef benthic assemblage structure, we sampled the benthic cover in an oiled coral reef area (hereafter indicated as O, represented by black cross in Fig. 1) and compared with that in two non-oiled reef areas (NO1 and NO2, hereafter denoted NOs; represented by green cross in Fig. 1). We selected the non-oiled areas based on their similarity in size (900 m2), reef structure composition (biogenic coral reef) and environmental conditions (i.e., intertidal, wave exposure and distance of the coast) to the oiled area. The non-oiled areas, where oil stains were not found, were 1.5 km apart. We used an asymmetrical design to compare the benthic cover between O and NOs. This design, with two non-oiled (“control”) locations (NOs), produces better estimates of natural variability than the use of a single “control” area, which was appropriate for this situation in which there was only a single impacted location (O) that could not be replicated (see Underwood 1992UNDERWOOD AJ. 1992. Beyond BACI: the detection of environmental impacts on populations in the real, but variable world. J Exp Mar Biol Ecol 161: 145-178. doi:10.1016/0022-0981(92)90094-Q., Glasby 1997GLASBY TM. 1997. Analysing data from post-impact studies using asymmetrical analyses of variance: a case study of epibiota on marinas. Aust J Ecol 22: 448-459. doi:10.1111/j.1442-9993.1997. tb00696.x., Terlizzi et al. 2005aTERLIZZI A, BENEDETTI-CECCHI L, BEVILACQUA S, FRASCHETTI S, GUIDETTI P & ANDERSON M. 2005a. Multivariate and univariate asymmetrical analyses in environmental impact assessment: a case study of Mediterranean subtidal sessile assemblages. Mar Ecol Prog Ser 289: 27-42. doi:10.3354/meps289027., bTERLIZZI A, SCUDERI D, FRASCHETTI S & ANDERSON MJ. 2005b. Quantifying effects of pollution on biodiversity: a case study of highly diverse molluscan assemblages in the Mediterranean. Mar Biol 148: 293-305. doi:10.1007/s00227-005-0080-8., Miranda et al. 2016MIRANDA RJ, CRUZ ICS & BARROS F. 2016. Effects of the alien coral Tubastraea tagusensis on native coral assemblages in a southwestern Atlantic coral reef. Mar Biol 163: 45. DOI 10.1007/s00227-016-2819-9.). Therefore, our design had two factors: Treatment (O and NOs, fixed and orthogonal) and Area (O, NO1 and NO2 random, nested in Treatment).

Between December 2019 January 2020, we characterized the benthic assemblages on intertidal reefs by walking using photo-quadrats (0.5 x 0.5 m) along 20 m transects. We haphazardly took 120 photographs per area (O, NO1 and NO2), 40 in each transect (n=3). We estimated the percentage of benthic cover per species through 30 randomly distributed points per photo-quadrat (3,600 points per area, 1,200 per transect) using the Coral Point Count with Excel Extensions Software (CPCe) (http://www.nova.edu/ocean/cpce/) (Kohler & Gill 2006KOHLER KE & GILL SM. 2006. Coral point count with excel extensions (CPCe): a visual basic program for the determination of coral and substrate coverage using random point count methodology. Comput Geosci 32: 1259-1269. doi:10.1016/j.cageo.2005.11.009.). The benthic categories included scleractinian corals, zoanthids such as Palythoa caribaeorum and Zoanthus sociatus, sea urchins, hydroids, macroalgae, turf algae, crustose coralline algae, calcareous articulated algae, Halimeda spp. and non-biotic categories as reef substrate and oil stains.

To evaluate potential oil effects on coral species vitality we monitored Siderastrea stellata colonies (n=2) in the intertidal arenite reef (Fig. 1) 30, 60 and 90 days after oil contact (November and December 2019 and January 2020). We used photo-quadrats (0.25 x 0.25 m) and visual observations to analyse signals of vitality decrease as bleaching, tecidual necrosis, diseases, decreases in corallite numbers or algae overgrowth.

Data analysis

We analysed the data using multivariate procedures to evaluate the variations in the structure of benthic assemblages. We used a permutational multivariate analysis of variance (PERMANOVA, Anderson 2001ANDERSON MJ. 2001. A new method for non-parametric multivariate analyses of variance. Austral Ecol 26: 32-46. doi:10.1111/j.1442-9993.2001.01070.pp.x.) to test for differences between assemblages in O and NOs, based on Bray–Curtis dissimilarities using 9999 random permutations. To check homogeneity of dispersions we used a permutational analysis of dispersions (PERMDISP) with untransformed data. The analyses were conducted in PRIMER 6+Permanova with a significance level (α) of 0.05.

RESULTS

Oil occurrence on the reefs

Our survey showed that the oil stains were found in two reef sites located in area locally called as Boqueirão beach, in Japaratinga, Alagoas (Figs. 1 and 2). Oil stains varied between 0.5 and 150 cm and were found in the holes, crest, crevices, and tide pools in the two intertidal reef sites, one with 4,200 m2 (arenite reef, Fig. 2a-b d-e and g-h) and one more with 900 m2 (coral reef, Fig. 1 c-d; Fig. 2c and f). No oil stains were found in subtidal reefs inside or around no-take and tourism areas in the APACC.

Figure 2
a-b) Massive oil occurrence on the Japaratinga reefs, marine protected area Costa dos Corais, Alagoas, Brazil in 17 October 2019 including habitats as c) hole, d) crest, e) tide pools, and contacting reef species as f) crustose coralline algae, g-h) scleractinian coral Siderastrea stellata. Photos: a-e, g-h) Ricardo J. Miranda; f) Pedro Pereira.

Evaluation of oil effects on benthic assemblage structure and coral vitality

The top five most abundant benthic categories (mean cover ≥1 %) in the intertidal coral reef were reef substrate (49.4 ± 9.9, mean ± SE %), hydroids (21.5 ± 6.6), calcareous articulated algae (CAA, 11.1 ± 5.5), macroalgae (6.9 ± 4.3) and zoanthids (2.8 ± 1.5). The scleractinian coral cover was low (0.3 ± 0.1) represented by species S. stellata and Favia gravida. The PERMANOVA did no detected significant differences in the cover patterns of benthic assemblages between O and NOs (Table I, Fig. 3), but differences were found between NOs (Table I). In the oiled reef area, the oil stains covered 0.8 ± 0.3 and the most abundant benthic groups were hydroids (33.3 ± 8.2), reef substrate (29.9 ± 4.3), CAA (27.6 ± 10.0) and zoanthids (5.6 ± 3.6) (Fig. 4). In the non-oiled areas, reef substrate cover predominated (49.5 ± 18.1 in NO1 and 68.7 ± 13.6 in NO2), but hydroids (26.9 ± 11.2), Halimeda spp. (12.3 ± 5.5), CAA (3.3 ± 0.5) and turf algae (3.1 ± 1.2) cover pattern in NO1 differed from macroalgae (19.0 ± 9.8), hydroids (4.5 ± 2.1), Halimeda spp. (2.6 ± 0.4) and CAA (2.4 ± 1.7) in NO2 (Fig. 4).

Figure 3
Multidimensional scaling (MDS) of benthic groups (i.e. relative cover of different organisms and abiotic categories) in oiled and non-oiled reef areas based on Bray–Curtis similarities of centroids of each replicate (photo-quadrats).
Figure 4
Mean cover (±SE) of benthic groups in oiled (O) and non-oiled (NO1 and NO2) reefs in Japaratinga, marine protected area Costa dos Corais, Alagoas, Brazil. COR=scleractinian corals, ZOA=zoanthids, URC=urchin, HYD=hydroid, MAC=macroalgae, TURF=filamentose turf algae, CCA=crustose coralline algae, CAA=calcareous articulated algae, HAL=Halimeda spp., RS=reef substrate, OIL=oil stain.
Table I
Asymmetrical PERMANOVA based on the Bray–Curtis dissimilarities (untransformed data) of the benthic assemblages.

Oil stains were observed directly contacting two colonies of the coral S. stellata, as well as sponges, crustose coralline algae and macroalgae species (Fig. 2). During three months following the oil spill, S. stellata colonies were apparently healthy and did not show signs of bleaching, tecidual necrosis, diseases, decrease in corallites or algal overgrowth.

DISCUSSION

We provide evidence that the crude oil from the largest spill disaster in Brazil reached APACC coral reefs and came into direct contact with coral, sponge, crustose coralline algae and macroalgae species. Crude oil accumulated on two reef areas (coral and arenite reefs) within holes, crevices, and tidal pools. However, oil cover found on the reef was low and we did not find differences in patterns of benthic cover structure between oiled and non-oiled reefs. Additionally, the scleractinian coral colonies as S. stellata that had direct contact with the oil did not show a loss of vitality (bleaching, tecidual necrosis, disease presence or algal overgrowth) during the three-month monitoring period.

Previous studies show that oil state, quantity and exposure duration can strongly influence the impacts of oil exposure on species and communities (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., Shafir et al. 2007SHAFIR S, VAN RIJN J & RINKEVICH B. 2007. Short and long term toxicity of crude oil and oil dispersants to two representative coral species. Environ Sci Technol 14: 5571-5574.). In fact, the crude state of the oil and the quick action of the volunteers, who quickly removed the oil from the study area (Fig. 5) almost certainly minimized negative short effects on the studied reefs. The crude oil spilled from an unknown source probably passed over numerous submerged reefs and accumulated on the intertidal reefs and mostly on sand beaches and estuaries. Environmental factors such as tide and wave action may also have influenced the accumulation of oil on intertidal reefs.

Figure 5
Oil remotion activities performed for volunteers between October 2019 and January 2020 during a massive spill episode in Japaratinga, marine protected area Costa dos Corais, Alagoas, Brazil. Photos: Ricardo J. Miranda.

The coral species monitored (S. stellata) is known to be tolerant of a wide amplitude of variation of physical/chemical conditions and water quality, which may have conferred heightened resistance to crude and dissolved oil, at least in the short-term. Others common or endemic corals of Southwest Atlantic may be particularly tolerant to stress conditions; for example, Mussismilia harttii showed the capacity to quickly remove heavy crude oil from its surface by producing mucus, gas bubbles and mesenterial filaments (Santos et al. 2020SANTOS HF, SANTOS LFA, JESUS HE, LACERDA CHF & MIES M. 2020. The South Atlantic coral Mussismilia harttii actively and quickly removes heavy crude oil from its surface. Bull Mar Sci 96: 803-804. https://doi.org/10.5343/bms.2020.0017.
https://doi.org/.https://doi.org/10.5343...
) which effectively reduced exposure to the toxic water-soluble fraction (Santos et al. 2015SANTOS HF ET AL. 2015. Impact of oil spills on coral reefs can be reduced by bioremediation using probiotic microbiota. Sci Rep 5: 18268. https://doi.org/10.1038/srep18268.
https://doi.org/.https://doi.org/10.1038...
). However, the relative resistance of these coral species to acute negative effects of crude oil must not be interpreted as a lack of impacts on species and coral reef health. Chronic oil impacts are known to disturb coral growth and metabolism (Loya & Rinkevich 1980LOYA Y & RINKEVICH B. 1980. Effects of oil pollution on coral reef communities. Mar Ecol Prog Ser 3: 167-180.), and reduce the number of reproductively viable coral colonies, gametes, life expectancy, as well as modifying planulae behaviour (Guzmán & Holst 1993GUZMÁN HM & HOLST I. 1993. Effects of chronic oil-sediment pollution on the reproduction of the Caribbean reef coral Siderastrea siderea. Coral Reefs 26: 276-282.). As chronic impacts that reduce coral health can appear over longer time frames (Bak 1987BAK RPM. 1987. Effects of Chronic Oil Pollution on a Caribbean Coral Reef. Mar Pollut Bull 18: 534-539.), the investigation of specific aspects of coral biology (e.g., growth, reproduction, bleaching susceptibility and metagenomics) are needed to comprehensively assess the long-time consequences of this oil spill on the APACC coral communities.

Although declines in the number of accidents and quantity of oil spilled into the world’s oceans have been reported over the last decades (Burgherr 2007BURGHERR P. 2007. In-depth analysis of accidental oil spills from tankers in the context of global spill trends from all sources. J of Hazard Mater 140: 245-256.), the massive oil spill described in present study and another recent episode off Mauritius in 2020 (Seveso et al. 2021SEVESO D, LOUIS YD, MONTANO S, GALLI P & SALIU F. 2021. The Mauritius Oil Spill: What’s Next? Pollutants 1: 18-28. https:// doi.org/10.3390/pollutants1010003.
https://doi.org/.https://doi.org/10.3390...
) demonstrates that coral reefs are still vulnerable to oil pollution. Even though volunteers quickly removed a significant quantity of crude oil, this was not enough to avoid ongoing environmental and social-economic consequences. For example, traces of ingestion of oil were observed in microzooplankton, key organisms to coral heterotrophy that represent the base of marine food webs (Campelo et al. 2021CAMPELO RPS, LIMA CDM, SANTANA CS, SILVA AJ, NEUMANN-LEITÃO S, FERREIRA BP, SOARES MO, MELO-JÚNIOR M & MELO PAM. 2021. Oil spills: the invisible impact on the base of tropical marine food webs. Mar Pollut Bull 167: 112281. https://doi. org/10.1016/j.marpolbul.2021.112281.). Government inaction, weak coordination and delayed actions in response to the spill (Brum et al. 2019BRUM HD, CAMPOS-SILVA JV & OLIVEIRA EG. 2019. Brazil oil spill response: government inaction. Science 367: 155-156.) amplified this social tragedy for traditional coastal communities, affecting human health and key economic activities such as fishing and tourism (Soares et al. 2020bSOARES MO, TEIXEIRA CEP, BEZERRA LEA, ROSSI S, TAVARES TCL & CAVALCANTE RM. 2020b. Brazil oil spill response: time for coordination. Science 367(6474): 155. https://doi.org/10.1126/science.aaz9993.
https://doi.org/.https://doi.org/10.1126...
, Magris & Giarrizzo 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., Estevo et al. 2021ESTEVO MO, LOPES PFM, OLIVEIRA-JÚNIOR JGC, JUNQUEIRA AB, SANTOS APO, LIMA JAS, MALHADO ACM, LADLE RJ & CAMPOS-SILVA JV. 2021. Immediate social and economic impacts of a major oil spill on Brazilian coastal fishing communities. Mar Pollut Bull 164: 111984. doi:10.1016/j.marpolbul.2021.111984., Zacharias et al. 2021ZACHARIAS DC, GAMA CM & FORNARO A. 2021. Mysterious oil spill on Brazilian coast: Analysis and estimates. Mar Pollut Bull 165: 112-125. doi: 10.1016/j.marpolbul.2021.112125.). The socio-ecological consequences of the oil spill associated with a growing interest in oil exploration in the region (ANP 2020ANP. 2020. Estudo Ambiental de Área Sedimentar (EAAS) da Bacia de Sergipe-Alagoas/Jacuípe. Available in: http://www.anp.gov.br/arquivos/atuacao/ep/ssm/estudo-seal-jacuipe/versao-consolidada-eaas-seal-jacuipe.pdf. Date Access: 27/06/2021.
http://www.anp.gov.br/arquivos/atuacao/e...
), highlights the importance for long-term monitoring to provide a broader view of the threat of oil pollution in the region. Thus, we recommend the continuation of long-time monitoring of socio-ecological aspects in APACC reefs, including oil effects on coral biology, trophic interactions and fishing and tourism activities. These strategies will contribute to a robust assessment of the chronic oil impacts, supporting mitigation and restoration actions that will be needed in the future.

ACKNOWLEDGMENTS

This work is part of the Long Term Ecological Research – Brazil site PELD-CCAL (Projeto Ecológico de Longa Duração -Costa dos Corais, Alagoas) funded by the Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq (#441657/2016-8, #442237/2020-0) and Fundação de Amparo à Pesquisa do Estado de Alagoas – FAPEAL (#60030.1564/2016, #PLD2021010000001 and 60030.0000000747/2019). RJL and ACMM are funded by CNPq (#309879/2019-1; #309980/2018-6) and European Union’s Horizon 2020 research and innovation programme (#854248). We thank all students and collaborators of the PELD-CCAL, Projeto Corais do Brasil, Projeto Conservação Recifal and Projeto Meros do Brasil for valuable help in the field or reef mapping, specially Nicoli Albuquerque, Tiago Albuquerque, Ana Maria Bruno Thiago Hara and Valberth Nunes, and all volunteers which contributed to oil remotion on the beach.

REFERENCES

  • ANP. 2020. Estudo Ambiental de Área Sedimentar (EAAS) da Bacia de Sergipe-Alagoas/Jacuípe. Available in: http://www.anp.gov.br/arquivos/atuacao/ep/ssm/estudo-seal-jacuipe/versao-consolidada-eaas-seal-jacuipe.pdf Date Access: 27/06/2021.
    » http://www.anp.gov.br/arquivos/atuacao/ep/ssm/estudo-seal-jacuipe/versao-consolidada-eaas-seal-jacuipe.pdf
  • ALAGOAS. 2020. Reunião Ordinária 300, Conselho Estadual de Proteção Ambiental do Estado de Alagoas – 11 de Fevereiro 2020. Available in: https://www.youtube.com/watch?v=fzhkIFBB2IY Data Access: 10/03/2021.
    » https://www.youtube.com/watch?v=fzhkIFBB2IY
  • ANDERSON MJ. 2001. A new method for non-parametric multivariate analyses of variance. Austral Ecol 26: 32-46. doi:10.1111/j.1442-9993.2001.01070.pp.x.
  • BAK RPM. 1987. Effects of Chronic Oil Pollution on a Caribbean Coral Reef. Mar Pollut Bull 18: 534-539.
  • BRASIL. 2013. Portaria ICMBIO n° 144 de 01 de Fevereiro de 2012. Aprova o Plano de Manejo da Área de Proteção Ambiental Costa dos Corais.
  • BRASIL. 2016. Portaria ICMBIO n° 19 de 09 de Março de 2016. Aprova o Plano de Ação Nacional para a Conservação dos Ambientes Coralíneos - PAN Corais.
  • BRUM HD, CAMPOS-SILVA JV & OLIVEIRA EG. 2019. Brazil oil spill response: government inaction. Science 367: 155-156.
  • BURGHERR P. 2007. In-depth analysis of accidental oil spills from tankers in the context of global spill trends from all sources. J of Hazard Mater 140: 245-256.
  • CAMPELO RPS, LIMA CDM, SANTANA CS, SILVA AJ, NEUMANN-LEITÃO S, FERREIRA BP, SOARES MO, MELO-JÚNIOR M & MELO PAM. 2021. Oil spills: the invisible impact on the base of tropical marine food webs. Mar Pollut Bull 167: 112281. https://doi. org/10.1016/j.marpolbul.2021.112281.
  • ESCOBAR H. 2020. Mysterious oil spill threatens marine biodiversity haven in Brazil. Science. https://doi.org/10.1126/science.aba1003
    » https://doi.org/10.1126/science.aba1003
  • ESTEVO MO, LOPES PFM, OLIVEIRA-JÚNIOR JGC, JUNQUEIRA AB, SANTOS APO, LIMA JAS, MALHADO ACM, LADLE RJ & CAMPOS-SILVA JV. 2021. Immediate social and economic impacts of a major oil spill on Brazilian coastal fishing communities. Mar Pollut Bull 164: 111984. doi:10.1016/j.marpolbul.2021.111984.
  • FERREIRA B & MAIDA M. 2006. Monitoramento dos Recifes de Coral do Brasil. Ministério do Meio Ambiente, Brasília.
  • GLASBY TM. 1997. Analysing data from post-impact studies using asymmetrical analyses of variance: a case study of epibiota on marinas. Aust J Ecol 22: 448-459. doi:10.1111/j.1442-9993.1997. tb00696.x.
  • GUZMÁN HM & HOLST I. 1993. Effects of chronic oil-sediment pollution on the reproduction of the Caribbean reef coral Siderastrea siderea. Coral Reefs 26: 276-282.
  • GUZMÁN HM, JACKSON JBC & WEIL E. 1991. Short-term ecological consequences of a major oil spill on Panamanian subtidal reef corals. Coral Reefs 10: 1-12.
  • HUGHES TP ET AL. 2017. Coral reefs in the Anthropocene. Nature 546: 82-90.
  • IBAMA - INSTITUTO BRASILEIRO DO MEIO AMBIENTE E DOS RECURSOS NATURAIS. 2020. Manchas de Óleo, Litoral Brasileiro: Localidades atingidas. Available in: http://www.ibama.gov.br/manchasdeoleo-localidades-atingidas Date Access: 20/06/2021.
    » http://www.ibama.gov.br/manchasdeoleo-localidades-atingidas
  • JACKSON JBC ET AL. 1989. Ecological effects of a major oil spill on Panamanian coastal marine communities. Science 243: 37-44.
  • KOHLER KE & GILL SM. 2006. Coral point count with excel extensions (CPCe): a visual basic program for the determination of coral and substrate coverage using random point count methodology. Comput Geosci 32: 1259-1269. doi:10.1016/j.cageo.2005.11.009.
  • LEÃO ZMAN, KIKUCHI RKP & TESTA V. 2003. Corals and coral reefs of Brazil. In: CORTÉS J (Ed), Latin America corals reefs, Amsterdam: Elsevier, p. 9-52.
  • LOYA Y & RINKEVICH B. 1980. Effects of oil pollution on coral reef communities. Mar Ecol Prog Ser 3: 167-180.
  • MAGRIS RA & GIARRIZZO T. 2020. Mysterious oil spill in the Atlantic Ocean threatens marine biodiversity and local people in Brazil. Mar Pollut Bull 153: 110961.
  • MAIDA M & FERREIRA BP. 1997. Coral reefs of Brazil: An overview. Panamá: Proc 8th Int Coral Reef Symp 1: 263-274.
  • MIRANDA RJ, ALMEIDA ECG, PINTO TK, SAMPAIO CLS, PEREIRA PHC, NUNES JACC & LADLE RJ. 2020a. Oil spill disaster in Brazil: impact assessment neglecting unique coral reefs. Science 366: 6466. sciencemag.org/content/366/6466/672/tab-eletters.
  • MIRANDA RJ ET AL. 2020b. Integrating Long Term Ecological Research (LTER) and Marine Protected Area management: challenges and solutions. Oecol Aust 24: 279-300.
  • MIRANDA RJ, CRUZ ICS & BARROS F. 2016. Effects of the alien coral Tubastraea tagusensis on native coral assemblages in a southwestern Atlantic coral reef. Mar Biol 163: 45. DOI 10.1007/s00227-016-2819-9.
  • PEREIRA PHC, MACEDO CH, NUNES JACC, MARANGONI LFB & BIANCHINI A. 2018. Effects of depth on reef fish communities: Insights of a “deep refuge hypothesis” from Southwestern Atlantic reefs. PLoS ONE 13(9): e0203072. https://doi.org/10.1371/journal.pone.0203072.
    » https://doi.org/.» https://doi.org/10.1371/journal.pone.0203072
  • PETERSON 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.
  • SANTOS HF ET AL. 2015. Impact of oil spills on coral reefs can be reduced by bioremediation using probiotic microbiota. Sci Rep 5: 18268. https://doi.org/10.1038/srep18268.
    » https://doi.org/.» https://doi.org/10.1038/srep18268
  • SANTOS HF, SANTOS LFA, JESUS HE, LACERDA CHF & MIES M. 2020. The South Atlantic coral Mussismilia harttii actively and quickly removes heavy crude oil from its surface. Bull Mar Sci 96: 803-804. https://doi.org/10.5343/bms.2020.0017.
    » https://doi.org/.» https://doi.org/10.5343/bms.2020.0017
  • SEVESO D, LOUIS YD, MONTANO S, GALLI P & SALIU F. 2021. The Mauritius Oil Spill: What’s Next? Pollutants 1: 18-28. https:// doi.org/10.3390/pollutants1010003.
    » https://doi.org/.» https://doi.org/10.3390/pollutants1010003
  • SHAFIR S, VAN RIJN J & RINKEVICH B. 2007. Short and long term toxicity of crude oil and oil dispersants to two representative coral species. Environ Sci Technol 14: 5571-5574.
  • SISSINI MN ET AL. 2020. Brazil oil spill response: Protect rhodolith beds. Science 367: 156.
  • SOARES MO ET AL. 2020a. Oil spill in South Atlantic (Brazil): Environmental and governmental disaster. Mar Policy 115: 103879.
  • SOARES MO, TEIXEIRA CEP, BEZERRA LEA, ROSSI S, TAVARES TCL & CAVALCANTE RM. 2020b. Brazil oil spill response: time for coordination. Science 367(6474): 155. https://doi.org/10.1126/science.aaz9993.
    » https://doi.org/.» https://doi.org/10.1126/science.aaz9993
  • TERLIZZI A, BENEDETTI-CECCHI L, BEVILACQUA S, FRASCHETTI S, GUIDETTI P & ANDERSON M. 2005a. Multivariate and univariate asymmetrical analyses in environmental impact assessment: a case study of Mediterranean subtidal sessile assemblages. Mar Ecol Prog Ser 289: 27-42. doi:10.3354/meps289027.
  • TERLIZZI A, SCUDERI D, FRASCHETTI S & ANDERSON MJ. 2005b. Quantifying effects of pollution on biodiversity: a case study of highly diverse molluscan assemblages in the Mediterranean. Mar Biol 148: 293-305. doi:10.1007/s00227-005-0080-8.
  • UNDERWOOD AJ. 1992. Beyond BACI: the detection of environmental impacts on populations in the real, but variable world. J Exp Mar Biol Ecol 161: 145-178. doi:10.1016/0022-0981(92)90094-Q.
  • ZACHARIAS DC, GAMA CM & FORNARO A. 2021. Mysterious oil spill on Brazilian coast: Analysis and estimates. Mar Pollut Bull 165: 112-125. doi: 10.1016/j.marpolbul.2021.112125.

Publication Dates

  • Publication in this collection
    23 May 2022
  • Date of issue
    2022

History

  • Received
    16 Mar 2021
  • Accepted
    9 Sept 2021
Academia Brasileira de Ciências Rua Anfilófio de Carvalho, 29, 3º andar, 20030-060 Rio de Janeiro RJ Brasil, Tel: +55 21 3907-8100 - Rio de Janeiro - RJ - Brazil
E-mail: aabc@abc.org.br