Submitted:
11 November 2025
Posted:
13 November 2025
You are already at the latest version
Abstract
Keywords:
1. Introduction
2. Materials and Methods
3. Results
3.1. Reports of Sargassum Landings in Brazil
3.1.1. 2014, Salinópolis/PA
3.1.2. 2015, Northern and Northeastern Brazil
3.1.3. 2021, Carutapera/MA
3.1.3. 2021, Porto de Galinhas/PE
3.2. Problems and Solutions to Sargassum in Brazil
3.2.1. Gas Emission and Health Risks from Sargassum
3.2.2. Uses of Stranded Sargassum as Building Materials
4. Discussion
4.1. Stranded Sargassum in Brazil
4.2. Patterns of Sargassum Occurrence in Brazil
4.3. Risks and Impacts on People and Animals
4.4. Impacts on Tourism and Social-Economy
4.5. Removal, Destinations and Potential Uses of Sargassum in Construction
4.6. Lessons Learned and Management Recommendations for Brazil
5. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- C. Colombo. Diários da descoberta da América: as quatro viagens e o testamento. L&PM, 1492.
- J. Murray. The discovery of America by Columbus: The Influences which led up to that Great Event, and its Effect on the Development of Oceanographical Knowledge. Scott. Geogr. Mag. 1893, 9, 561–586. [Google Scholar] [CrossRef]
- G. E. R. Deacon. The Sargasso Sea. Geogr. J. 1942, 99, 16–28. [Google Scholar] [CrossRef]
- J. F. R. Gower and S. A. King. Distribution of floating Sargassum in the Gulf of Mexico and the Atlantic ocean mapped using MERIS. Int. J. Remote Sens. 2011, 32, 1917–1929. [Google Scholar] [CrossRef]
- M. D. Guiry et al.. AlgaeBase: An On-line Resource for Algae. 2014, 35, 105–115. [CrossRef]
- K. S. T. Alleyne, D. Johnson, F. Neat, H. A. Oxenford, and H. Vallѐs. Seasonal variation in morphotype composition of pelagic Sargassum influx events is linked to oceanic origin. Sci. Rep. 2023, 13. [Google Scholar] [CrossRef]
- J. Gower and S. King. Seaweed, seaweed everywhere. Science (80-.). 2019, 364, 27. [Google Scholar] [CrossRef]
- R. E. Rodríguez-Martínez, E. G. Torres-Conde, and E. Jordán-Dahlgren. Pelagic Sargassum cleanup cost in Mexico. Ocean Coast. Manag. 2023, 237. [Google Scholar] [CrossRef]
- J. Gower, E. Young, and S. King. Satellite images suggest a new Sargassum source region in 2011. Remote Sens. Lett. 2013, 4, 764–773. [Google Scholar] [CrossRef]
- E. M. Johns et al. The establishment of a pelagic Sargassum population in the tropical Atlantic: Biological consequences of a basin-scale long distance dispersal event. Prog. Oceanogr. 2020, 182. [Google Scholar] [CrossRef]
- J. N. Butler and A. W. Stoner. Pelagic Sargassum: has its biomass changed in the last 50 years? Deep Sea Res. Part A, Oceanogr. Res. Pap. 1984, 31, 1259–1264. [Google Scholar] [CrossRef]
- B. E. Lapointe. A comparison of nutrient-limited productivity in Sargassum natans from neritic vs. oceanic waters of the western North Atlantic Ocean. Limnol. Oceanogr. 1995, 40, 625–633. [Google Scholar] [CrossRef]
- V. Smetacek and A. Zingone. Green and golden seaweed tides on the rise. Nature 2013, 504, 84–88. [Google Scholar] [CrossRef]
- J. Gower, C. Hu, G. Borstad, and S. King. Ocean color satellites show extensive lines of floating sargassum in the gulf of Mexico. IEEE Trans. Geosci. Remote Sens. 2006, 44, 3619–3625. [Google Scholar] [CrossRef]
- M. Wang, C. Hu, B. B. Barnes, G. Mitchum, B. Lapointe, and J. P. Montoya. The great Atlantic Sargassum belt. Science (80-.). 2019, 364, 83–87. [Google Scholar] [CrossRef]
- M. T. M. de Széchy, P. M. Guedes, M. H. Baeta-Neves, and E. N. Oliveira. Verification of Sargassum natans (Linnaeus) Gaillon (Heterokontophyta: Phaeophyceae) from the Sargasso Sea off the coast of Brazil, western Atlantic Ocean. Check List 2012, 8, 638–641. [Google Scholar] [CrossRef]
- J. Trinanes, N. F. Putman, G. Goni, C. Hu, and M. Wang. Monitoring pelagic Sargassum inundation potential for coastal communities. J. Oper. Oceanogr. 2023, 16, 48–59. [Google Scholar] [CrossRef]
- N. F. Putman, R. Lumpkin, M. J. Olascoaga, J. Trinanes, and G. J. Goni. Improving transport predictions of pelagic Sargassum. J. Exp. Mar. Bio. Ecol. 2020, 529. [Google Scholar] [CrossRef]
- B. I. van Tussenbroek et al. Severe impacts of brown tides caused by Sargassum spp. on near-shore Caribbean seagrass communities. Mar. Pollut. Bull. 2017, 122, 272–281. [Google Scholar] [CrossRef]
- R. E. Rodríguez-Martínez et al. Faunal mortality associated with massive beaching and decomposition of pelagic Sargassum. Mar. Pollut. Bull. 2019, 146, 201–205. [Google Scholar] [CrossRef] [PubMed]
- R. E. Rodríguez-Martínez, E. Jordán-Dahlgren, and C. Hu. Spatio-temporal variability of pelagic Sargassum landings on the northern Mexican Caribbean. Remote Sens. Appl. Soc. Environ. 2022, 27. [Google Scholar] [CrossRef]
- C. A. Oviatt, K. Huizenga, C. S. Rogers, and W. J. Miller. What nutrient sources support anomalous growth and the recent sargassum mass stranding on Caribbean beaches? A review. Mar. Pollut. Bull. 2019, 145, 517–525. [Google Scholar] [CrossRef]
- P. Mohan and E. Strobl. Tourism and marine crises: The impact of Sargassum invasion on Caribbean small island developing sates. Ocean Coast. Manag. 2024, 251. [Google Scholar] [CrossRef]
- R. E. Liranzo-Gómez, D. García-Cortés, and U. Jáuregui-Haza. Adaptation and Sustainable Management of Massive Influx of Sargassum in the Caribbean. Procedia Environ. Sci. Eng. Manag. 2021, 8, 543–553. [Google Scholar]
- J. J. Milledge and P. J. Harvey. Golden Tides: Problem or golden opportunity? The valorisation of Sargassum from beach inundations. J. Mar. Sci. Eng. 2016, 4. [Google Scholar] [CrossRef]
- M. N. Sissini et al. The floating Sargassum (Phaeophyceae) of the South Atlantic Ocean - Likely scenarios. Phycologia 2017, 56, 321–328. [Google Scholar] [CrossRef]
- D. Moher et al.. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. PLoS Medicine 2009, 6. [Google Scholar] [CrossRef]
- M. Ouzzani, H. Hammady, Z. Fedorowicz, and A. Elmagarmid. Rayyan-a web and mobile app for systematic reviews. Syst. Rev. 2016, 5. [Google Scholar] [CrossRef]
- J. A. Rossignolo, A. J. Felicio Peres Duran, C. Bueno, J. E. Martinelli Filho, H. Savastano Junior, and F. G. Tonin. Algae application in civil construction: A review with focus on the potential uses of the pelagic Sargassum spp. biomass. J. Environ. Manage. 2022, 303. [Google Scholar] [CrossRef]
- C. Bueno et al.. Life Cycle Assessment Applied to End-of-Life Scenarios of Sargassum spp. for Application in Civil Construction. Sustain. 2023, 15. [Google Scholar] [CrossRef]
- M. da Silva Parente, G. P. Lyra, C. Bueno, F. G. Tonin, and J. A. Rossignolo. Holistic evaluation of ceramic clay properties with Sargassum spp. ash replacement. Constr. Build. Mater. 2024, 435. [Google Scholar] [CrossRef]
- G. P. Lyra, A. L. Colombo, A. J. F. P. Duran, I. M. da S. Parente, C. Bueno, and J. A. Rossignolo. The Use of Sargassum spp. Ashes Like a Raw Material for Mortar Production: Composite Performance and Environmental Outlook. Materials (Basel). 2024, 17. [Google Scholar] [CrossRef]
- J. F. P. Duran et al.. The Use of Sargasso Seaweed as Lignocellulosic Material for Particleboards: Technical Viability and Life Cycle Assessment. Buildings 2024, 14. [Google Scholar] [CrossRef]
- M. J. B. de Moraes et al.. Seaweed waste in eco-friendly construction materials: Valorization of Sargassum ash as a mineral addition in fiber cements. Clean. Circ. Bioeconomy 2024, 9. [Google Scholar] [CrossRef]
- T. M. Silva et al.. A custom, low-cost, continuous flow chamber built for experimental Sargassum seaweed decomposition and exposure of small rodents to generated gaseous products. Heliyon 2023, 9. [Google Scholar] [CrossRef]
- G. do N. Santos, O. S. Nascimento, F. dos A. Pedreira, G. I. Rios, J. N. C. Vasconcelos, and J. M. de C. Nunes. Análise Quali-Quantitativa Das Algas Arribadas Do Norte Do Estado Da Bahia, Brasil. Bras. Acta Bot. Malacit. 2013, 13, 13–24, http://www.biolveg.uma.es/abm/Volumenes/vol38/38_Santos.pdf. [Google Scholar]
- M. I. L. G. Cavalcanti, P. M. González Sánchez, and M. T. Fujii. Comparison of the diversity and biomass of beach-cast seaweeds from NE and SE Brazil. Eur. J. Phycol. 2022, 57, 367–376. [Google Scholar] [CrossRef]
- T. B. Harb and F. Chow. An overview of beach-cast seaweeds: Potential and opportunities for the valorization of underused waste biomass. Algal Res. 2022, 62, 102643. [Google Scholar] [CrossRef]
- de, G. PEDRINI, G. I. P. GUARINO, F. dos S. P. DINIZ, and J. E. MARTINELLI FILHO. Checklist of benthic algae from beaches and rocky outcrops on the northeast coast of Pará state, Brazilian Amazonia. Acta Amaz. 2021, 51, 166–170. [Google Scholar] [CrossRef]
- A. Nittrouer et al. Amazon Sediment Transport and Accumulation Along the Continuum of Mixed Fluvial and Marine Processes. Ann. Rev. Mar. Sci. 2021, 13, 501–536. [Google Scholar] [CrossRef]
- L. A. R. Iporac et al.. Community-based monitoring reveals spatiotemporal variation of sargasso inundation levels and morphotype dominance across the Caribbean and South Florida. Aquat. Bot. 2022, 182. [Google Scholar] [CrossRef]
- R. Aquino et al.. Possible Amazonian contribution to Sargassum enhancement on the Amazon Continental Shelf. Sci. Total Environ. 2022, 853. [Google Scholar] [CrossRef]
- J. C. Espinoza et al. The new record of drought and warmth in the Amazon in 2023 related to regional and global climatic features. Sci. Rep. 2024, 14. [Google Scholar] [CrossRef]
- J. Umbricht et al.. Nitrate Uptake and Primary Production Along the Amazon River Plume Continuum. J. Geophys. Res. Biogeosciences 2024, 129. [Google Scholar] [CrossRef]
- NSkliris, R. Marsh, K. Appeaning Addo, and H. Oxenford. Physical drivers of pelagic sargassum bloom interannual variability in the Central West Atlantic over 2010–2020. Ocean Dyn. 2022, 72, 383–404. [CrossRef]
- M. T. Brooks, V. J. Coles, R. R. Hood, and J. F. R. Gower. Factors controlling the seasonal distribution of pelagic Sargassum. Mar. Ecol. Prog. Ser. 2018, 599, 1–18. [Google Scholar] [CrossRef]
- J. Jouanno et al.. Evolution of the riverine nutrient export to the Tropical Atlantic over the last 15 years: Is there a link with Sargassum proliferation? Environ. Res. Lett. 2021, 16. [Google Scholar] [CrossRef]
- B. R. C. Tocci, L. M. Vieira, M. S. Tamanaha, and C. Resgalla Junior. Stranding events of drift organisms (Arribadas) in southern Brazil and the spread of invasive bryozoan in South America. Mar. Pollut. Bull. 2022, 184, 114120. [Google Scholar] [CrossRef]
- D. Resiere et al.. Sargassum seaweed health menace in the Caribbean: clinical characteristics of a population exposed to hydrogen sulfide during the 2018 massive stranding. Clin. Toxicol. 2020, 1–9. [CrossRef]
- D. A. Casas-Beltrán et al. Seaweed invasion! Temporal changes in beach conditions lead to increasing cenote usage and contamination in the Riviera Maya. Sustain. 2020, 12. [Google Scholar] [CrossRef]
- D. B. de Lanlay et al. Risk of preeclampsia among women living in coastal areas impacted by sargassum strandings on the French Caribbean island of Martinique. Environ. Toxicol. Pharmacol. 2022, 94, 103894. [Google Scholar] [CrossRef] [PubMed]
- D. A. Devault et al. The silent spring of Sargassum. Environ. Sci. Pollut. Res. 2021, 28, 15580–15583. [Google Scholar] [CrossRef]
- R. W. Mendonça, T. Theirlynck, E. R. Zettler, L. A. Amaral-Zettler, and M. C. Oliveira. Microbiome changes in a stranding simulation of the holopelagic macroalgae Sargassum natans and Sargassum fluitans. Ocean Coast. Res. 2024, 72. [Google Scholar] [CrossRef]
- S. Maurer, K. Gross, and S. P. Stapleton. Beached Sargassum alters sand thermal environments: Implications for incubating sea turtle eggs. J. Exp. Mar. Bio. Ecol. 2022, 546. [Google Scholar] [CrossRef]
- B. Solarin, D. A. Bolaji, O. S. Fakayode, and RO. Akinnigbagbe. Impacts of an invasive seaweed Sargassum hystrix var. fluitans (Børgesen 1914) on the fisheries and other economic implications for the Nigerian coastal waters. IOSR J. Agric. Vet. Sci. 2014, 7, 01–06. [Google Scholar] [CrossRef]
- S. F. Câmara, F. R. Pinto, F. R. da Silva, M. de O. Soares, and T. M. De Paula. Socioeconomic vulnerability of communities on the Brazilian coast to the largest oil spill (2019–2020) in tropical oceans. Ocean Coast. Manag. 2021, 202. [Google Scholar] [CrossRef]
- D. Robledo, E. Vázquez-Delfín, Y. Freile-Pelegrín, R. M. Vásquez-Elizondo, Z. N. Qui-Minet, and A. Salazar-Garibay. Challenges and Opportunities in Relation to Sargassum Events Along the Caribbean Sea. Front. Mar. Sci. 2021, 8. [Google Scholar] [CrossRef]
- IBAMA - Instituto Brasileiro do Meio Ambiente e dos Recursos Naturais Renováveis, Instrução Normativa N° 89, de 02 de fevereiro de 2006. Brasilia, DF: MMA, 2006.
- .-A. Cipolloni et al.. Metals and metalloids concentrations in three genotypes of pelagic Sargassum from the Atlantic Ocean Basin-scale. Mar. Pollut. Bull. 2022, 178, 113564. [Google Scholar] [CrossRef]
- Volesky, J. Weber, and R. Vieira. Biosorption of Cd and Cu by different types of Sargassum biomass. Process Metall. 1999, 9, 473–482. [Google Scholar] [CrossRef]
- Y. A. Fidai, J. Dash, E. L. Tompkins, and T. Tonon. A systematic review of floating and beach landing records of sargassum beyond the sargasso sea. Environ. Res. Commun. 2020, 2. [Google Scholar] [CrossRef]



Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).