Total mercury (T-Hg) in ichthyofauna with the highest consumption in San Marcos - Sucre, Colombia
Mercurio total (Hg-T) en ictiofauna de mayor consumo en San Marcos - Sucre, Colombia
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Objective. Hg was quantified in the dorsal muscle of the 11 species of fish most consumed in San Marcos, located in the region of La Mojana. Materials and methods. Dorsal muscle samples were taken from the fish species, T-Hg concentrations were quantified using cold vapor atomic absorption spectrophotometry (CVAAS). Results. The species with the highest Hg-T values were those with carnivorous eating habits: Pseudoplatystoma magdaleniatum (0.44 ± 0.09 µg/g), Plagioscion surinamensis (0.42 ± 0.14 µg/g) and Hoplias malabaricus (0.39 ± 0.11 µg/g). However, the maximum recommended amount of Hg in fish (0.5 µg/g) set by the European Union, was not exceeded by any of the species studied. Conclusions. It is concluded that the commercial ichthyofauna of La Mojana is contaminated by Hg, a result of the mining activities that take place in the channels of the rivers that discharge in this region. The persistent consumption of fish from the evaluated areas by its inhabitants represents a high risk, due to the high toxicity of Hg, which presents adverse effects on human health even when it is consumed in low doses for prolonged periods of time.
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- Beckers F, Rinklebe J. Cycling of mercury in the environment: Sources, fate, and human health implications: A review. Crit Rev Environ Sci Technol. 2017;47(9):693–794. https://doi:10.1080/10643389.2017.1326277
- Niane B, Guédron S, Feder F, Legros S, Ngom PM, Moritz R. Impact of recent artisanal small-scale gold mining in Senegal: Mercury and methylmercury contamination of terrestrial and aquatic ecosystems. Sci Total Environ. 2019;669:185–9.https:// doi:10.1016/j.scitotenv.2019.03.108
- Okpala COR, Sardo G, Vitale S, Bono G, Arukwe A. Hazardous properties and toxicological update of mercury: From fish food to human health safety perspective. Crit Rev Food Sci Nutr. 2018;58(12):1986–2001. https://doi:10.1080/10408398.2017.1291491
- P, Du B, Chan HM, Feng X. Human inorganic mercury exposure, renal effects and possible pathways in Wanshan mercury mining area, China. Environ Res. 2015;140:198–204. https://doi.org/10.1016/j.envres.2015.03.033
- Lavoie RA, Jardine TD, Chumchal MM, Kidd KA, Campbell LM. Biomagnification of mercury in aquatic food webs: a worldwide meta-analysis. Environ Sci Technol. 2013;47(23):13385–94. https://doi.org/10.1021/es403103t
- Pinedo-Hernández J, Marrugo-Negrete J, Díez S. Speciation and bioavailability of mercury in sediments impacted by gold mining in Colombia. Chemosphere. 2015;119:1289–95. https://doi: 10.1016/j.chemosphere.2014.09.044
- Marrugo Negrete J, Pinedo-Hernández J, Paternina-Uribe R, Quiroz-Aguas L, Pacheco-Florez S. Distribución espacial y evaluación de la contaminación ambiental por mercurio en la región de la Mojana, Colombia. Rev MVZ Cordoba. 2018;23(S):7062–75. https://doi.org/10.21897/rmvz.1481
- Díaz SM, Muñoz-Guerrero MN, Palma-Parra M, Becerra-Arias C, Fernández-Niño JA. Exposure to mercury in workers and the population surrounding gold mining areas in the Mojana region, Colombia. Int J Environ Res Public Health. 2018;15(11):2337. https://doi.org/10.3390/ijerph15112337
- Isaacs Cubides P. Rehabilitación del ecosistema de humedal en la región de la Mojana para mitigar efecto de las inundaciones. 2020 ; Available from: http://repository.humboldt.org.co/handle/20.500.11761/35508
- Evenson GR, Golden HE, Lane CR, McLaughlin DL, D’Amico E. Depressional wetlands affect watershed hydrological, biogeochemical, and ecological functions. Ecol Appl. 2018;28(4):953–66. https://doi:10.1002/eap.1701
- Marrugo-Negrete J, Pinedo-Hernández J, Marrugo-Madrid S, Díez S. Assessment of trace element pollution and ecological risks in a river basin impacted by mining in Colombia. Environ Sci Pollut Res Int. 2021;28(1):201–10. https://doi.org/10.1007/s11356-020-10356-4
- Marrugo-Negrete J, Vargas-Licona S, Ruiz-Guzmán JA, Marrugo-Madrid S, Bravo AG, Díez S. Human health risk of methylmercury from fish consumption at the largest floodplain in Colombia. Environ Res. 2020;182(109050):109050.https://doi.org/10.1016/j.envres.2019.109050
- Marrugo-Negrete J, Benítez LN, Olivero-Verbel J, Lans E, Vazquez Gutierrez F. Spatial and seasonal mercury distribution in the Ayapel Marsh, Mojana region, Colombia. Int J Environ Health Res. 2010;20(6):451–9. https://DOI: 10.1080/09603123.2010.499451
- Mojica JI, Vélez JCC. Libro rojo de peces dulceacuícolas de Colombia. 1st ed. Bogotá: Instituto de Investigación de Recursos Biológicos Alexander von Humboldt; 2012. http://hdl.handle.net/20.500.11761/34197
- Sadiq M, Zaidi TH, Al-Mohana H. Sample weight and digestion temperature as critical factors in mercury determination in fish. Bull Environ Contam Toxicol. 1991;47(3):335–41. https://doi: 10.1007/BF01702191.
- Atencio G V, Kerguelén D E, Naar E, Petro R. Desempeño reproductivo del bocachico Prochilodus magdalenae inducido dos veces en un mismo año. Rev MVZ Cordoba. 2013;3304–10. https://doi.org/10.21897/rmvz.192
- Jiménez-Segura LFF, Palacio J, López R. Características biológicas del blanquillo Sorubim cuspicaudus littmann; Burr y Nass, 2000 y Bagre rayado Pseudoplatystoma magnaleniatumBuitrago-Suárez y Burr, 2007 (Siluriformes: Pimelodidae). Actual Biol. 2009;31(90):1–14. https://revistas.udea.edu.co/index.php/actbio/article/view/4729
- Buendía Lara D, Argumedo Díaz J, Olaya-Nieto C, Segura-Guevara F, Brú-Cordero S, Tordecilla-Petro G. Biología reproductiva del blanquillo (Sorubim cuspicaudus Littmann et al., 2000) en la cuenca del Río Sinú, Colombia. Rev MVZ Cordoba. 2006;71–8. https://doi.org/10.21897/rmvz.1046
- Ibagón N, Maldonado-Ocampo JA, Cioffi M de B, Dergam JA. Chromosomal diversity of Hoplias malabaricus (Characiformes, erythrinidae) along the Magdalena river (Colombia—northern south America) and its significance for the neotropical region. Zebrafish. 2020;17(3):211–9. https://doi.org/10.1089/zeb.2019.1827
- Guimarães CBS, Pflanzer Junior SB, Pinheiro HP, Mendes TMF, Ueta MT. Centesimal composition and meat yield of Hoplias malabaricus: association with intestinal parasites. Braz J Vet Parasitol 2021; 30(1):e021120. https://doi.org/10.1590/S1984-29612021020
- Salazar-Camacho C, Salas-Moreno M, Paternina-Uribe R, Marrugo-Negrete J, Díez S. Mercury species in fish from a tropical river highly impacted by gold mining at the Colombian Pacific region. Chemosphere. 2021;264(Pt 2):128478. https://doi.org/10.1016/j.chemosphere.2020.128478
- Azevedo-Silva CE, Almeida R, Carvalho DP, Ometto JPHB, de Camargo PB, Dorneles PR, et al. Mercury biomagnification and the trophic structure of the ichthyofauna from a remote lake in the Brazilian Amazon. Environ Res. 2016;151:286–96. https://doi.org/10.1016/j.envres.2016.07.035
- Mille T, Bisch A, Caill-Milly N, Cresson P, Deborde J, Gueux A, et al. Distribution of mercury species in different tissues and trophic levels of commonly consumed fish species from the south Bay of Biscay (France). Mar Pollut Bull. 2021;166(112172):112172. https://doi.org/10.1016/j.marpolbul.2021.112172
- Segura-Guevara F, López-Corrales H, Medrano De La Hoz C, Olaya-Nieto CW. Biología reproductiva de Liseta Leporinus muyscorum Steindachner, 1901 en el río Sinú, Colombia. Rev MVZ Cordoba. 2017;22(1):5728–37. https://doi.org/10.21897/rmvz.932
- Morales J, García-Alzate CA. Ecología trófica y rasgos ecomorfológicos de Triportheus magdalenae (Characiformes: Triportheidae) en el embalse El Guájaro, cuenca baja del río Magdalena, Colombia. Rev Biol Trop. 2018;66(3):1208. https://doi.org/10.15517/rbt.v66i3.30621
- Paranjape AR, Hall BD. Recent advances in the study of mercury methylation in aquatic systems. Facets (Ott). 2017;2(1):85–119. https://doi.org/10.1139/facets-2016-0027
- Valdelamar Villegas JC. Apuntes sobre la importancia ecológica, ambiental y social de la arenca Triportheus magdalenae (Steindachner, 1878). Un ejemplo de endemismo invisibilizado. Intropica. 2018;152. https://doi.org/10.21676/23897864.2628
- Marrugo-Negrete J, Navarro-Frómeta A, Ruiz-Guzmán J. Total mercury concentrations in fish from Urrá reservoir (Sinú river, Colombia). Six years of monitoring. Rev MVZ Cordoba. 2015;20(3):4754–65. https://doi.org/10.21897/rmvz.45
- Qian Y, Cheng C, Feng H, Hong Z, Zhu Q, Kolenčík M, et al. Assessment of metal mobility in sediment, commercial fish accumulation and impact on human health risk in a large shallow plateau lake in southwest of China. Ecotoxicol Environ Saf. 2020;194(110346):110346. https://doi.org/10.1016/j.ecoenv.2020.110346
- López-Casas S, Jiménez-Segura LF, Agostinho AA, Pérez CM. Potamodromous migrations in the Magdalena River basin: bimodal reproductive patterns in neotropical rivers: Potamodromous migrations in the magdalena river basin. J Fish Biol. 2016;89(1):157–71. https://doi.org/10.1111/jfb.12941
- Argumedo G, Marcela P, Vergara C, Vidal JV, Marrugo-Negrete J. Evaluación de la concentración de mercurio en arroz (Oryza sativa) crudo y cocido procedente del municipio de San Marcos- Sucre y zona aurífera del municipio de Ayapel – Córdoba. Rev. Univ. Ind. Santander. 2015; 47(2), 169-177. https://revistas.uis.edu.co/index.php/revistasaluduis/article/view/4826
- Zapata L, Usma J. Guía de las especies Migratorias de la Biodiversidad en Colombia. Peces. Ministerio de Ambiente y Desarrollo Sostenible / WWF-Colombia. Bogotá, D.C. Colombia. 2013. Vol. 2. https://wwflac.awsassets.panda.org/downloads/migratoriaspeces_42_web_final.pdf
- Li H, Zheng D, Yang J, Wu C, Zhang S, Li H, et al. Salinity and redox conditions affect the methyl mercury formation in sediment of Suaeda heteroptera wetlands of Liaoning province, Northeast China. Mar Pollut Bull. 2019;142:537–43. https://doi.org/10.1016/j.marpolbul.2019.03.066
- Monteiro DA, Taylor EW, Rantin FT, Kalinin AL. Impact of waterborne and trophic mercury exposures on cardiac function of two ecologically distinct Neotropical freshwater fish Brycon amazonicus and Hoplias malabaricus. Comp Biochem Physiol C Toxicol Pharmacol. 2017;201:26–34. https://doi.org/10.1016/j.cbpc.2017.09.004
- Morcillo P, Angeles Esteban M, Cuesta A. Mercury and its toxic effects on fish. AIMS Environ Sci. 2017;4(3):386–402. https://doi.org/10.3934/environsci.2017.3.386
- Sun Y, Li Y, Rao J, Liu Z, Chen Q. Effects of inorganic mercury exposure on histological structure, antioxidant status and immune response of immune organs in yellow catfish (Pelteobagrus fulvidraco ): Mercury induces oxidative stress and immune response in immune organs. J Appl Toxicol. 2018;38(6):843–54. https://doi.org/10.1002/jat.3592
- Pereira P, Korbas M, Pereira V, Cappello T, Maisano M, Canário J, et al. A multidimensional concept for mercury neuronal and sensory toxicity in fish - From toxicokinetics and biochemistry to morphometry and behavior. Biochim Biophys Acta Gen Subj. 2019;1863(12):129298. https://doi.org/10.1016/j.bbagen.2019.01.020
- Olivero-Verbel J, Carranza-Lopez L, Caballero-Gallardo K, Ripoll-Arboleda A, Muñoz-Sosa D. Human exposure and risk assessment associated with mercury pollution in the Caqueta River, Colombian Amazon. Environ Sci Pollut Res Int. 2016;23(20):20761–71. https://doi.org/10.1007/s11356-016-7255-3
- Calao CR, Marrugo JL. Efectos genotóxicos en población humana asociados a metales pesados en la región de La Mojana, Colombia, 2013. Biomedica [Internet]. 2015;35(0). Available from: https://doi.org/10.7705/biomedica.v35i0.2392
- Rice KM, Walker EM Jr, Wu M, Gillette C, Blough ER. Environmental mercury and its toxic effects. J Prev Med Public Health. 2014;47(2):74–83. https://doi.org/10.3961/jpmph.2014.47.2.74
- Oliveira LF, Rodrigues LD, Cardillo GM, Nejm MB, Guimarães-Marques M, Reyes-Garcia SZ, et al. Deleterious effects of chronic mercury exposure on in vitro LTP, memory process, and oxidative stress. Environ Sci Pollut Res Int. 2020;27(7):7559–69. https://doi.org/10.1007/s11356-019-06625-6