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Is it safe to consume medicinal plants in mined areas? Investigating possible effects caused by a metal-contaminated plant in southern Brazil

ABSTRACT

Mineral extraction areas are a significant environmental concern due to soil, water, and plant food resources contamination. Some medicinal plant species, such as those of the genus Baccharis, potentially bioaccumulate toxic elements. We evaluate the metal content from coal mining activity present in Baccharis sagittalis and in the soil; and whether this plant consumption represents a risk to human health. Cd and Pb presented levels that exceed those recommended by three global health agencies. Cd and Pb showed high levels in the projections of the daily intake recommended by international health agencies. After interviewing local residents close to mining areas, we found that 53.8 % of the interviewees mentioned the consumption of Baccharis sagittalis as infusion. These results indicate that the consumption of metal-contaminated Baccharis sagittalis can cause health problems as those metals accumulate in the human body. However, studies on Al, Ba, Cr, Cu, Mn, Ni, and Zn acceptable levels in plants consumed by humans are scarce. The contamination of plant species with associated traditional use close to mining areas can increase food security vulnerability of people who live near those areas and are constantly exposed to these agents, using plants gathered in the region.

Keywords:
mining; medicinal plants; traditional communities; metals; human health.

Introduction

Mineral extraction has a vital role in the economy, especially in developing countries, yet it is responsible for environmental stress such as soil and water resources contamination (Weiler et al. 2015Weiler AM, Hergesheimer C, Brisbois B, et al. 2015. Food sovereignty, food security and health equity: A meta-narrative mapping exercise. Health Policy Plan 30: 1078-1092. ; Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.). Investment in mining and the search for new extraction areas have grown in recent years. Studies point that by 2050, mineral extraction fields and the number of metal-contaminated locations will have doubled (Schrecker et al. 2018Schrecker T, Birn AE, Aguilera M. 2018. How extractive industries affect health: Political economy underpinnings and pathways. Health and Place 52: 135-47. ; Candeias et al. 2019Candeias C, Ávila P, Coelho P, Teixeira JP. 2019. Mining activities: Health impacts. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. Amsterdam, Elsevier. p. 415-435. ; Farjana et al. 2019Farjana SH, Huda N, Parvez Mahmud MA, Saidur R. 2019. A review on the impact of mining and mineral processing industries through life cycle assessment. Journal of Cleaner Production 231: 1200-1217. ). In countries such as China, South Africa, and Brazil, the extraction of mineral resources presents environmental concerns due to an increase in contaminated areas (Kemper et al. 1994Kemper C, Gibbs P, Obendorf D, Marvanek S, Lenghaus C. 1994. A review of heavy metal and organochlorine levels in marine mammals in Australia. Science of the Total Environment 154: 129-39.; Quinn et al. 2011Quinn CH, Ziervogel G, Taylor A, Takama T, Thomalla F. 2011. Coping with multiple stresses in rural South Africa. Ecology and Society 16: 1-21.; Maitland et al. 2016Maitland BM, Poesch M, Anderson AE, Pandit SN. 2016. Industrial road crossings drive changes in community structure and instream habitat for freshwater fishes in the boreal forest. Freshwater Biology 61: 1-18.; Elyamine et al. 2018Elyamine A, Moussa M, Ismael M, et al. 2018. Earthworms, Rice Straw, and Plant Interactions Change the Organic Connections in Soil and Promote the Decontamination of Cadmium in Soil. International Journal of Environmental Research and Public Health 15: 2398. ; Zeng et al. 2019Zeng L, Guo J, Wang B, Jun LV, Wang Q. 2019. Analyzing sustainability of Chinese coal cities using a decision tree modeling approach. Resources Policy 64: 1-12.). Environmental impacts caused by mining range from changes in the landscape (e.g., removal of plant species and soil layers) to changes in ecological interactions dynamics (e.g., favoring of species that manage to survive in the impacted area and the removal of essential vegetable species for the local fauna), and contamination from different metals (Blanco et al. 2020Blanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.a; Feng et al. 2020Feng L, Yan H, Dai C, et al. 2020. The systematic exploration of cadmium-accumulation characteristics of maize kernel in acidic soil with different pollution levels in China. Science of the Total Environment 729: 138972.). However, even though these countries are increasing economic investments in the mineral sector, there is insufficient knowledge about the levels at which these elements are available in the environment, whether plants absorb them, and whether they represent a risk to human health (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.).

Some metals are released into the environment as byproducts during extraction (Della Bosca & Gillespie 2018Della Bosca H, Gillespie J. 2018. The coal story: Generational coal mining communities and strategies of energy transition in Australia. Energy Policy 120: 734-740.). In coal extractions, for example, pyrite release generates acid drainage that intensifies mineral weathering, producing high quantities of these minerals in the water and soil. Some of these metals, such as copper (Cu), manganese (Mn), and zinc (Zn) (Duffus 2002Duffus J. 2002. “Heavy metals” - A meaningless term? Pure and Applied Chemistry 74: 793-807. ; Campos et al. 2003Campos ML, Almeida JA, Souza LS. 2003. Avaliação de três áreas de solo construído após mineração de carvão a céu aberto em Lauro Müller, Santa Catarina. Revista Brasileira de Ciência do Solo 27: 1123-1137.; Ashraf et al. 2019Ashraf S, Ali Q, Zahir ZA, Ashraf S, Asghar HN. 2019. Phytoremediation: Environmentally sustainable way for reclamation of heavy metal polluted soils. Ecotoxicology and Environmental Safety 174: 714-727.; Li et al. 2020Liu B, Ai S, Zhang W, Huang D, Zhang Y. 2017. Assessment of the bioavailability, bioaccessibility and transfer of heavy metals in the soil-grain-human systems near a mining and smelting area in NW China. Science of the Total Environment 609: 822-829.), contribute to biologically essential functions like nitrogen availability in the soil for plants’ growth and development. When available in low quantities, they do not present a risk to the functioning of ecosystem dynamics and human health (Licina et al. 2007Licina V, Antic-Mladenovic S, Kresovic M. 2007. The accumulation of heavy metals in plants (Lactuca sativa L., Fragaria vesca L.) after the amelioration of coalmine tailing soils with different organo-mineral amendments. Archives of Agronomy and Soil Science 53: 39-48.; Oti 2015Oti WO. 2015. Bioaccumulation factors and pollution indices of heavy metals in selected fruits and vegetables from a derelict mine and their associated health implications. International journal of sustainable built environment 4: 15-23. ). However, at high levels (i.e., Cu above 29 mg.kg-1 and Zn above 39 mg.kg-1 in soil) (Ashraf et al. 2019Ashraf S, Ali Q, Zahir ZA, Ashraf S, Asghar HN. 2019. Phytoremediation: Environmentally sustainable way for reclamation of heavy metal polluted soils. Ecotoxicology and Environmental Safety 174: 714-727.) or in unexploitable forms (i.e., lacking a biological function in the system) such as cadmium (Cd) and lead (Pb), these metals can cause toxic effects to the ecosystem and human health (Duffus 2002Duffus J. 2002. “Heavy metals” - A meaningless term? Pure and Applied Chemistry 74: 793-807. ). This toxicity is directly related to the exposure time and considers levels that exceed those recommended by health agencies (Li et al. 2020Li C, Sanchez GM, Wu Z, et al. 2020. Spatiotemporal patterns and drivers of soil contamination with heavy metals during an intensive urbanization period (1989-2018) in southern China. Environment Pollution 260: 114075. ).

A few plant species that grow in mining areas can accumulate metals at levels greater than those recommended by national and international surveillance centers (Ashraf et al. 2019Ashraf S, Ali Q, Zahir ZA, Ashraf S, Asghar HN. 2019. Phytoremediation: Environmentally sustainable way for reclamation of heavy metal polluted soils. Ecotoxicology and Environmental Safety 174: 714-727.). Species of the genus Baccharis, with occurrence in North and South America, have been studied for their medicinal qualities and their capacity to grow naturally in mining areas due to their ability to accumulate metals (Carreira 2007Carreira RC. 2007. Baccharis trimera (Less.) DC. (Asteraceae): estudo comparativo dos óleos voláteis, atividade biológica e crescimento de estacas de populações ocorrentes em áreas de Cerrado e Mata Atlântica. PhD Thesis, São Paulo University, São Paulo.; Souza et al. 2007Souza PZ de, Costa S, Zocche JJ. 2007. Baccharis trimera Less. DC. como indicadora da recuperação de áreas mineradas de carvão. Revista Brasileira de Biociências 5: 702-704.; Haque et al. 2008Haque N, Peralta-Videa JR, Jones GL, Gill TE, Gardea-Torresdey JL. 2008. Screening the phytoremediation potential of desert broom (Baccharis sarothroides Gray) growing on mine tailings in Arizona, USA. Environment Pollution 153: 362-378. ; Menezes et al. 2013Menezes APS, Da Silva J, Roloff J, et al. 2013. Baccharis trimera (Less.) DC. as genotoxicity indicator of exposure to coal and emissions from a thermal power plant. Archives of Environmental Contamination and Toxicology 65: 434-441.; Paula et al. 2016Paula A, Menezes S, Fisher C, et al. 2016. Chemical and toxicological effects of medicinal Baccharis trimera extract from coal burning area. Chemosphere 146: 396-404.). In coal mining areas in southern Brazil, B. trimera contained high levels of Mn (i.e., above 2.3 mg in 200 mL) and Zn (i.e., above 11 mg in 200 mL) in their leaves, compared to these metals’ availability in the soil (Souza et al. 2007Souza PZ de, Costa S, Zocche JJ. 2007. Baccharis trimera Less. DC. como indicadora da recuperação de áreas mineradas de carvão. Revista Brasileira de Biociências 5: 702-704.). The aqueous extract of B. trimera from coal mining areas displayed a mutagenic effect in animal cells, with high levels of cellular damage (Menezes et al. 2015Menezes APS, Da Silva J, Rossato RR, et al. 2015. Genotoxic and biochemical changes in Baccharis trimera induced by coal contamination. Ecotoxicology and Environmental Safety 114: 9-16.), along with genotoxic effects in in vitro blood cells (Menezes et al. 2015Menezes APS, Da Silva J, Rossato RR, et al. 2015. Genotoxic and biochemical changes in Baccharis trimera induced by coal contamination. Ecotoxicology and Environmental Safety 114: 9-16.; Paula et al. 2016Paula A, Menezes S, Fisher C, et al. 2016. Chemical and toxicological effects of medicinal Baccharis trimera extract from coal burning area. Chemosphere 146: 396-404.). In B. sarothroides leaves, present in copper mining areas in the United States, scientists observed hyperaccumulation of Cu, Pb, chromium (Cr), Zn, arsenic (As), and nickel (Ni) (Haque et al. 2008Haque N, Peralta-Videa JR, Jones GL, Gill TE, Gardea-Torresdey JL. 2008. Screening the phytoremediation potential of desert broom (Baccharis sarothroides Gray) growing on mine tailings in Arizona, USA. Environment Pollution 153: 362-378. ). In addition to this situation, some species of the genus Baccharis are known widely and used for medicinal purposes in Brazil, being recognized as such by the National Health Surveillance Agency (ANVISA) and presented in the National List of Medicinal Plants of Interest to the Unified Health System (RENISUS) from Brazil (Marmitt et al. 2015Marmitt DJ, Rempel C, Goettert MI, Silva AC. 2015. Plantas com potencial antibacteriano da relação nacional de plantas medicinais de interesse do sistema único de saúde: revisão sistemática. Revista de Saúde Pública de Santa Catarina 8: 135-151.).

The proximity increase of mining areas to human populations, including indigenous peoples and traditional and local communities, has grown in the last 20 years, generating territorial conflicts and food insecurity (Alonso et al. 2018Alonso EB, Cockx L, Swinnen J. 2018. Culture and food security. Global Food Security 17:113-127. ; Horowitz et al. 2018Horowitz LS, Keeling A, Lévesque F, Rodon T, Schott S, Thériault S. 2018. Indigenous peoples’ relationships to large-scale mining in post/colonial contexts: Toward multidisciplinary comparative perspectives. Extractive Industries and Society 5: 404-414. ; Vega et al. 2018Vega CM, Orellana JDY, Oliveira MW, Hacon SS, Basta PC. 2018. Human mercury exposure in yanomami indigenous villages from the Brazilian Amazon. International Journal of Environmental Research and Public Health 15: 1-13. ). Ensuring food security is a challenge in the 21st century since, in addition to providing food for everyone, guaranteeing its safety is also needed (Marrugo-Negrete et al. 2020Marrugo-Negrete J, Vargas-Licona S, Ruiz-Guzmán JA, Marrugo-Madrid S, Bravo AG, Díez S. 2020. Human health risk of methylmercury from fish consumption at the largest floodplain in Colombia. Environmental Research 182: 109050.). However, due to the proximity increase to contaminated areas, indigenous peoples and traditional and local communities’ health and food security are threatened; these populations are three-four times more vulnerable to diseases from unhealthy or unsafe food (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.; Marrugo-Negrete et al. 2020Marrugo-Negrete J, Vargas-Licona S, Ruiz-Guzmán JA, Marrugo-Madrid S, Bravo AG, Díez S. 2020. Human health risk of methylmercury from fish consumption at the largest floodplain in Colombia. Environmental Research 182: 109050.). This vulnerability is partially due to food contamination from metals produced by mineral extraction (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.). In countries such as China, which accounts for one of the largest volumes of coal mining worldwide, solutions to ensure food safety (Juric et al. 2018Juric AK, Batal M, David W, et al. 2018. Risk assessment of dietary lead exposure among First Nations people living on-reserve in Ontario, Canada using a total diet study and a probabilistic approach. Journal of hazardous materials 344: 55-63. ; Sun et al. 2019Sun Y, Li H, Guo G, Semple KT, Jones KC. 2019. Soil contamination in China: Current priorities, defining background levels and standards for heavy metals. Journal of Environmental Management 251: 1-7. ) include an environmental safety law and a resolution for acceptable levels of metals in food and tea (Ghose 2014Ghose B. 2014. Food security and food self-sufficiency in China: From past to 2050. Food Energy Security 3: 86-95.; Yi et al. 2018Yi K, Fan W, Chen J, et al. 2018. Annual input and output fluxes of heavy metals to paddy fields in four types of contaminated areas in Hunan Province, China. Science of the Total Environment 634: 67-76.). However, few studies have analyzed food security and the contamination of food and medicinal plants consumed by local communities living close to mined areas (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.; Blanco et al. 2020Blanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.a).

In coal extraction areas in southern Brazil, there is a mosaic of mining areas within human communities that use vegetable species for food and medicine (Blanco et al. 2020Blanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.a). Many of these rural and urban neighborhoods established themselves specifically to support mining activity, occupying regions extremely close to the mines (Blanco et al. 2020aBlanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11., bBlanco GD, Hanazaki N, Cunha SMB, Cremer MJ, Campos ML. 2020b. Exploring the interfaces between ethnobiology and ecotoxicology: A novel approach. Ethnobiology Letters 11: 29-37. ). In these areas, many Baccharis species known as carqueja are found, including Baccharis sagittalis, B. trimera, and B. sarothroides, all traditionally used as medicine (Santos et al. 2008Santos R, Citadini-Zanette V, Leal-Filho LS, Hennies WT. 2008. Spontaneous vegetation on overburden piles in the coal basin of Santa Catarina, Brazil. Restoration Ecology 16: 444-452. ; Karam et al. 2013Karam TK, Dalposso LM, Casa DM, De Freitas GBL. 2013. Carqueja (Baccharis trimera): Utilização terapêutica e biossíntese. Revista Brasileira de Plantas Medicinais 15: 280-286. ; Stolz et al. 2014Stolz ED, Müller LG, Trojan-Rodrigues M, et al. 2014. Survey of plants popularly used for pain relief in Rio Grande do Sul, southern Brazil. Brazilian Journal of Pharmacognosy 24: 185-196. ) B. sagittalis, commonly consumed as an infusion, is abundant and occurs spontaneously in these areas (Blanco et al. 2020aBlanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.). Thus, this study aimed to investigate the contents of aluminum (Al), barium (Ba), Cd, Cr, Cu, Mn, Ni, Pb, and Zn in B. sagittalis, the frequency of this species’ consumption by local people, and whether it represents a risk. The tested hypothesis is that in mining areas, B. sagittalis contains high levels of those metals, and its consumption can endanger human health.

Materials and methods

Data collection

Data was acquired in the Santa Catarina coal basin, the second biggest coal-mining region in Brazil. Six mined areas with Baccharis sagittalis (Less.) DC (Asteraceae) (voucher EAFM16711) occurrence were selected; three of these areas (S 28°32'34.6'' W 049°29'34.8'' Lauro Muller, S 27°31'56.9'' W 048°30'44.4'' Urussanga, and S 28°29'54.1'' W 049°22'57.9'' Treviso) experienced extensive coal mining activity (until coal depletion). In these areas, Al, Ba, Cd, Cr, Cu, Pb, Mn, and Zn presence in the soil had already been detected (Campos et al. 2010Campos ML, Almeida JA, Berto C, et al. 2010. Impactos no solo provocados pela mineração e depósito de rejeitos de carvão mineral. Revista Ciência Agroveterinária 9: 198-205.; Hugen et al. 2013Hugen C, Miquelluti DJ, Campos ML, et al. 2013. Cu and Zn contents in soil profiles of different lithologies in Santa Catarina. Revista Brasileira de Engenharia Agrícola e Ambiental 17: 622-638. ; Souza et al. 2016Souza LC de, Campos ML, Reichert G, Moura CN. 2016. Teores de Arsênio em solos de três regiões do estado de Santa Catarina. Revista Ambiente e Água 9: 445-458.), with no record of other anthropic activities affecting soil composition. The other three areas (S 28°32'33.2'' W 049°20'53.6'' Lauro Muller, S 28°32'34.5'' W 049°29'34.8'' Urussanga, and S 28°29'54.7'' W 049°22'57.5'' Treviso) were close to the mining areas ones but sustained no record of mineral exploration or anthropogenic activity (Fig. 1). The distance between mined and unmined areas spanned a maximum of 10 Km. Two transects were covered in each of the six collection areas, comprising ten whole individuals collected 15 m to 20 m apart. For each plant, the soil was obtained through three sub-samples, collected with the aid of an auger, at a depth of 20 cm. These subsamples were combined into a single sample for each individual of B. sagittalis and then air dried. To avoid contamination of samples from one collection to another, the auger was cleaned after each collection. In total, 60 individuals and 60 soil samples were obtained (i.e., 30 samples from mined areas and 30 samples from unmined areas).

Figure 1
Map of samples areas in southern Brazil. Ten samples of B. sagittalis and soil were collected in each of the six locations identified on the map. Triangles represent unmined areas and circles represent mined ones.

Preparation and analysis of soil samples

After pulverizing the samples to a fine powder in an agate mortar and straining them in a 0.149 mm sieve, they were subjected to acid digestion following the USEPA 3050 B method (USEPA 1996USEPA. United States Environmental Justice Implementation. 1996. Enforcement and Compliance Plan Assurance (220 1 A). Washington, DC: Office of Environmental Justice 1996. https://www.epa.gov/sites/production/files/2015 02/documents/implementation_plan_ej_1996.pdf.
https://www.epa.gov/sites/production/fil...
). Method reliability measurement was performed using a reference soil material CRM-Agro E2002a (EMBRAPA 2015EMBRAPA. 2015. Brazilian Agricultural Research Company. Materiais de Referência para a Agricultura, Pecuária e Toxicologia: Solo Código: RM-Agro E2002a. https://iopscience.iop.org/article/10.1088/1742-6596/733/1/012005.
https://iopscience.iop.org/article/10.10...
) and cell samples for the Qualitative Limit of Detection (QLD) (Tab. 1). Then, The Instrument Detection Limits (IDL) according to APHA was calculated (APHA 2017APHA. 2017. Generation Public Health. American Public Health Association 89. https://www.apha.org/what-is-public-health/generation-public-health. 07 Jul. 2021.
https://www.apha.org/what-is-public-heal...
). All analyses were performed in duplicate.

At last, Al, Ba, Cd, Cr, Cu, Pb, Mn, and Zn contents were quantified in an inductively coupled plasma optical emission spectrometer (ICP-OES); and Ni content in an air-acetylene flame atomic absorption spectrometer (F-AAS).

Preparation and analysis of plant material

Analysis in B. sagittalis samples comprised the same metals quantified in soil samples. The plants were weighed and dried in a greenhouse at 45° C for 42 hours, and dried again in 12 hours intervals to constant weight. The samples were macerated and stored for subsequent opening via the USEPA 3050 B method (USEPA 1996USEPA. United States Environmental Justice Implementation. 1996. Enforcement and Compliance Plan Assurance (220 1 A). Washington, DC: Office of Environmental Justice 1996. https://www.epa.gov/sites/production/files/2015 02/documents/implementation_plan_ej_1996.pdf.
https://www.epa.gov/sites/production/fil...
). The reliability of the analytical method was assessed using a reference sample from the CRM-Agro E1001a - Brachiaria Brizantha leaves (EMBRAPA 2013EMBRAPA. 2013. Brazilian Agricultural Research Company. Materiais de Referência para a Agricultura, Pecuária e Toxicologia: Brachiaria Brizantha cv Marandu Código: RM-Agro E1001a. https://iopscience.iop.org/article/10.1088/1742-6596/733/1/012005.
https://iopscience.iop.org/article/10.10...
).

Interviews and daily ingestion

After getting their informed consent, semi-structured interviews were conducted with residents of the communities found at a maximum distance of 300 m from the mined areas, individually, between February and March 2018. A total of 14 local communities (Vila Funil, Rio Carvão, Barreiros, Guaitá, Cidade Alta, Vila Visconde, São Sebastião Alto, Vila São Jorge, Rio Fiorita, Volta Redonda, Campo Morozini, Santa Luzia, Santa Augusta, and São Sebastião), belonging to 6 municipalities (Criciúma, Forquilhinha, Siderópolis, Treviso, Urussanga, and Lauro Müller) were selected to take part in the study, given their historical background in mining activity. Within each community, house visits were paid only once, and interviews were conducted exclusively with those interested in participating in the research. Interviewees were questioned if they knew and consumed B. sagittalis, where they usually collected it, and asked about its consumption frequency. For measurement of B. sagittalis consumption frequency, each interviewee answered how many cups (200 mL) they ingested per week (see Text S1 for the questionnaire used). Three levels (De Godoy et al. 2013De Godoy RCB, Deliza R, Gheno LB, Licodiedoff S, Frizon CNT, Ribani RH. 2013. Consumer perceptions, attitudes and acceptance of new and traditional mate tea products. International food research journal 53: 801-817. ) were used to classify residents’ frequency of B. sagittalis ingestion: small (i.e., once a week or less), medium (i.e., two-three times over the week), and frequent (i.e., four-seven times a week or more). Based on worldwide information on the consumption of one tea bag (on average each bag is 2 g) per preparation. A consumption projection of 2 g per cup (200 ml) was performed and the estimate was calculated, as a rule of three, of the intake associated with Cd, Cr, Cu and Pb (based on the values indicated by international and national agencies (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
; Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
https://apps.fas.usda.gov/newgainapi/api...
).

Statistical Analysis

Generalized linear models (GLMs) were used to compare the differences in metal concentrations in B. sagittalis leaves from mined and unmined areas. All models met the premises of normality and homoscedasticity, and for each metal, a model was created using a gamma distribution family. For graphical representation, boxplots were generated. Parameters followed ANVISA RDC resolution no 42 of August 29, 2013, for Brazil (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
), as well as maximum contamination levels for China (Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
https://apps.fas.usda.gov/newgainapi/api...
) and the European Union (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.), given that both provide reference values for acceptable levels of many metals in herbs and infusions (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
; Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
https://apps.fas.usda.gov/newgainapi/api...
).

Results

The reference values of the elements Al, Ba, Cd, Cr, Cu, Mn, Ni, Pb and Zn for the soil and Baccharis sagittalis are reported in Tab. 1 and 2, respectively. The values obtained were compared with a reference base, with the values of CRM-Agro E2002a for the soil and for B. sagittalis the values of CRM-Agro E1001a.

Table 1
Reference obtained values of the elements. Al, Ba, Cd, Cr, Cu, Mn, Ni, Pb and Zn of the reference sample CRM-Agro E2002a (EMBRAPA 2015EMBRAPA. 2015. Brazilian Agricultural Research Company. Materiais de Referência para a Agricultura, Pecuária e Toxicologia: Solo Código: RM-Agro E2002a. https://iopscience.iop.org/article/10.1088/1742-6596/733/1/012005.
https://iopscience.iop.org/article/10.10...
) and Instrumental Detection Limit (IDL) (APHA 2017APHA. 2017. Generation Public Health. American Public Health Association 89. https://www.apha.org/what-is-public-health/generation-public-health. 07 Jul. 2021.
https://www.apha.org/what-is-public-heal...
). Metals were quantified by ICP-OES, except for Ni, which was quantified by F-AAS.
Table 2
Reference obtained values of the elements. Al, Ba, Cd, Cr, Cu, Mn, Ni, Pb and Zn of the reference sample CRM-Agro E1001a - Brachiaria Brizantha leaves (EMBRAPA 2013EMBRAPA. 2013. Brazilian Agricultural Research Company. Materiais de Referência para a Agricultura, Pecuária e Toxicologia: Brachiaria Brizantha cv Marandu Código: RM-Agro E1001a. https://iopscience.iop.org/article/10.1088/1742-6596/733/1/012005.
https://iopscience.iop.org/article/10.10...
) and Instrumental Detection Limit (IDL) (APHA 2017APHA. 2017. Generation Public Health. American Public Health Association 89. https://www.apha.org/what-is-public-health/generation-public-health. 07 Jul. 2021.
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). Metals were quantified by ICP-OES, except for Ni, which was quantified by F-AAS.

The average contents of metals quantified in the soil samples are reported in Table 3. Al, Mn, and Pb were present in higher concentrations in soil from mined areas (16453.97 ± 2235.53 mg.kg-1, 308.22 ± 224.96 mg.kg-1, and 15.80 ± 9.69 mg.kg-1, respectively) when compared to unmined areas (14594.98 ± 5132.04 mg.kg-1, 87.92 ± 69.49 mg.kg-1, and 11.86 ± 5.51 mg.kg-1, respectively) (p < 0.05). The samples from unmined areas showed higher contents of Cr, Cu, and Ni (10.46 ± 2.98 mg.kg-1, 41.63 ± 12.11 mg.kg-1, and 18.05 ± 5.50 mg.kg-1, respectively) in comparison to samples from mined ones (8.18 ± 3.48 mg.kg-1, 22.13 ± 9.91 mg.kg-1, and 13.86 ± 4.23 mg.kg-1, respectively) (p < 0.05). The contents of Ba, Cd, and Zn showed nonsignificant variations between the two sampled groups (p ≥ 0.05).

Table 3
Average contents (mg.kg-1) and standard deviation. Al, Ba, Cd, Cr, Cu, Pb, Mn and Zn in the soil of mined and unmined areas of Santa Catarina. Both P and T values of comparisons between metal concentrations in mined and unmined areas are presented, as well as total metal concentrations allowed for the state of Santa Catarina. SD: Standard Deviation; VRQ SC: Quality reference values for Santa Catarina.

Al and Mn had the highest mean concentration in mined soil with a high standard deviation (16453.97 ± 2235.53 mg.kg-1 and 308.22 ± 224.96 mg.kg-1, respectively). Considering reference levels from Santa Catarina state, Cr and Cd showed values above the acceptable level (5 mg.kg-1 and 0.12 mg.kg-1, respectively) (Hugen et al. 2013Hugen C, Miquelluti DJ, Campos ML, et al. 2013. Cu and Zn contents in soil profiles of different lithologies in Santa Catarina. Revista Brasileira de Engenharia Agrícola e Ambiental 17: 622-638. ; Souza et al.2016Souza LC de, Campos ML, Reichert G, Moura CN. 2016. Teores de Arsênio em solos de três regiões do estado de Santa Catarina. Revista Ambiente e Água 9: 445-458.), both in mined and unmined soil. In addition, Cu also presented concentration levels above the allowed, in unmined areas (29 mg.kg-1) (Hugen et al. 2013Hugen C, Miquelluti DJ, Campos ML, et al. 2013. Cu and Zn contents in soil profiles of different lithologies in Santa Catarina. Revista Brasileira de Engenharia Agrícola e Ambiental 17: 622-638. ) (Tab. 3).

In plant specimens, Ba, Cd, Mn, and Zn showed higher concentrations in leaves of individuals collected in mined areas (11.69 ± 10.25 mg.kg-1, 0.30 ± 0.09 mg.kg-1, 335.8 ± 212.60 mg.kg-1, and 23.34 ± 9.51 mg.kg-1, respectively) when compared to those obtained from unmined ones (3.64 ± 1.84 mg.kg-1, 0.25 ± 0.04 mg.kg-1, 263.87 ± 79.58 mg.kg-1, and 17.83 ± 3.81 mg.kg-1, respectively) (p < 0.05). Al and Cr were the only metals that showed a higher content in plant leaves collected from unmined areas in comparison to samples from mined areas (Tab. 4).

Table 4
Average contents (mg.kg-1). Al, Ba, Cd, Cr, Cu, Pb, Mn and Zn in B. sagittalis leaves from unmined and mined areas of Santa Catarina. Both P and T values of comparisons between metal concentrations in mined and unmined areas are presented, SD: Standard Deviation.

Concerning maximum concentrations of Pb (0.60 mg.kg-1) allowed for herbs and teas in Brazil (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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), these metals presented showed levels higher than recommended for consumption (Tab. 5). The maximum concentrations of Cd and Pb presented levels higher than recommended for consumption for China and the European Union (Cd: above 1 mg.kg-1 for China and 0.05 mg.kg-1 for European Union; Pb: above 5 mg.kg-1 for China and 1 mg.kg-1 for European Union) (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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)(Tab. 5). References for Al, Ba, Cr, Cu, Mn, Ni, and Zn maximum contents in teas and infusions were not found throughout the literature. Both metals with a significant difference in concentration between mined and unmined areas and metals with concentrations higher than recommended (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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) can be observed in Fig. 2. Pb presented values above the allowed limits in Brazil and European Union (above 0.60 mg.kg-1 and 1 mg.kg-1, respectively) (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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). Similar to the observed in soil, Mn and Pb contents were higher in leaf samples from mined areas, while leaf samples from unmined ones showed higher values of Al (Tab. 4).

Table 5
Average contents (mg.kg-1). Cd, Cr, Cu, and Pb found in B. sagittalis leaves and their maximum recommended values in herbs consumption in Brazil, China, and the European Union.

Figure 2
Boxplot of Al, Ba, Cd, Cr, Cu, Mn, Ni, Pb and Zn contents (mg. Kg-1) in plants from mined and unmined areas in Santa Catarina. The red dotted line indicates the maximum reference values allowed for Cd and Pb in Brazil, according to ANVISA resolution45 (2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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); the blue dotted line indicates the maximum reference values allowed for Cd and Pb for China, according to Westman46 resolution (2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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); and the brown dotted line indicates the maximum allowable reference levels for Pb in the European Union according to the resolution of Soliman47 (2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.). Different letters indicate significant difference (p < 0.05) of the element concentration between plants from unmined and mined areas.

Both metals with a significant difference in concentration between mined and unmined areas and metals with concentrations higher than recommended (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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) can be observed in Figure 2. Pb presented values above the allowed limits in Brazil and the European Union (above 0.60 mg.kg-1 and 1 mg.kg-1, respectively) (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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). Similar to the observed in soil, Mn and Pb contents were higher in leaf samples from mined areas, while leaf samples from unmined ones showed higher values of Al (Tab. 4).

In total, 195 residents were interviewed, with an average of 14 residents (± 5.4) per location. Their age ranged from 15 to 86 years old, with a mean of 53 years (± 17.8). Among the interviewees, 130 were women (68 %), and 66 were men (32 %). Of all, 105 (53.8 %), who were mainly over 50 years old (74.2 %) and women (70.4 %), claimed to consume B. sagittalis as tea (infusion). Within this group, 96 interviewees (91.4 %) mentioned a small consumption frequency (once a week), 1.9 % reported an average one (two-three times a week), and 6.6 % of respondents mentioned a frequent B. sagittalis infusion consumption (four-seven times a week or more). Intake amount varied from one to two cups for most of the interviewees (95.7 %), with the intake of one cup (200 mL) being the most mentioned (46.6 %), followed by one-two cups (200 mL each) (44.7 %). Among interviewees who declared to consume B. sagittalis, 8.5 % do it with the infusion of yerba mate or "chimarrão" (Ilex paraguariensis).

Using published information on the use of 2 g of B. sagittalis per infusion preparation and based on indicators (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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; Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
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), estimates of Cd, Cr, Cu, and Pb consumption per respondent were calculated (Tab. 6). Cd value was higher than the limit recommended by the European Union (< 0.10 x 10-3 mg.kg-1 in 2 g of vegetable dry matter) (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.) (Tab. 6). Pb value was higher than those recommended by both Brazil (< 1.12 x 10-3 mg.kg-1 in 2 g of vegetable dry matter) (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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) and the European Union (< 2 x 10-3 mg.kg-1 in 2 g of vegetable dry matter) (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.) (Tab. 6). However, all projections (Tab. 6) considered values of B. sagittalis dry leaves instead of its leaf infusion; therefore, depending on the method of infusion preparation, these results can vary.

Table 6
Estimates of daily intake in mg of Cd, Cr, Cu, and Pb in 2 g of B. sagittalis dry matter, and acceptable metal concentration values in herbs consumption in Brazil, China, and the European Union. Based on the values in Table 5, a rule of three was used to predict the amount of intake of elements per preparation.

Discussion

Individuals of B. sagittalis from both mined and unmined areas in Santa Catarina presented high contents of metals that can be toxic to human health if consumed. However, the concentration of analyzed metals differed between soil and plant samples from mined and unmined areas. Al, Mn, and Pb had higher percentages in the mined area soil, while Ba, Cd, Mn, and Zn prevailed in plant samples in the mined area. Meanwhile, Cr, Cu, Ni and Zn have higher soil concentrations in unmined areas, in the plant of these same areas only Al showed higher concentrations. According to reference values for Santa Catarina, Cd and Cr concentrations in soil were above the recommended in both mined and unmined areas (Souza et al. 2016Souza LC de, Campos ML, Reichert G, Moura CN. 2016. Teores de Arsênio em solos de três regiões do estado de Santa Catarina. Revista Ambiente e Água 9: 445-458.) (above 0.12 mg.kg-1 and 5 mg.kg-1, respectively). Cu concentration in the soil was also above the recommended levels in the state, but in unmined areas only (above 29 mg.kg-1) (Hugen et al. 2013Hugen C, Miquelluti DJ, Campos ML, et al. 2013. Cu and Zn contents in soil profiles of different lithologies in Santa Catarina. Revista Brasileira de Engenharia Agrícola e Ambiental 17: 622-638. ). Also, in estimates considering consumption of 2 g of B. sagittalis dry matter, Cd and Pb, also had values above the recommended in the European Union (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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) (i.e., Cd < 0.10x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.) and Pb < 2 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.)), and Pb above the recommended in the Brazil (i.e., Pb < 1.2 x 10-3 mg.kg-1 47 (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
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)) (Tab. 6). These figures are worrisome, as 53.8 % of respondents said they consume this species as infusion in the region.

Among the metals with elevated concentrations in the soil and B. sagittalis leaves, Al and Mn stood out. Aluminum results may be due to Santa Catarina’s soil traits, with naturally higher availability of this element, a feature observed in other soils as well (Quitaes 2000Quintaes KD. 2000. Utensílios para alimentos e implicações nutricionais. Revista de Nutrição 13: 151-156. ; Echart & Cavalli-Molina 2001Echart CL, Cavalli-Molina S. 2001. Aluminum phytotoxicity: effects, tolerance mechanisms and its genetic control. Ciência Rural 31: 531-541.; Cunha 2018Cunha M GO de, Almeida JA de, Ernani PR, et al. 2018. Chemical Species and aluminum concentration in the solution of acid soils cultivated with soybean and corn under liming. Revista Brasileira de Ciência do Solo 42: 1-16.; Suppi et al. 2018Suppi IM, Campos ML, Miquelluti DJ, Bueno DK. 2018. Cobalt and manganese content in soils of Santa Catarina. Revista de Ciências Agroveterinárias 17: 579-588. ). In addition, anthropogenic actions may alter the ways in which Al is available in the environment, ultimately changing plants’ capacity to absorb this metal (Echart & Cavalli-Molina 2001Echart CL, Cavalli-Molina S. 2001. Aluminum phytotoxicity: effects, tolerance mechanisms and its genetic control. Ciência Rural 31: 531-541.). Such an effect could be accountable for the high concentrations of Al found in plants from unmined areas, even though levels of this metal were higher in the soil samples from mined areas (Cunha 2018Cunha M GO de, Almeida JA de, Ernani PR, et al. 2018. Chemical Species and aluminum concentration in the solution of acid soils cultivated with soybean and corn under liming. Revista Brasileira de Ciência do Solo 42: 1-16.; Suppi et al. 2018Suppi IM, Campos ML, Miquelluti DJ, Bueno DK. 2018. Cobalt and manganese content in soils of Santa Catarina. Revista de Ciências Agroveterinárias 17: 579-588. ). Al consumption may be related to the development of kidney problems and early stages of Alzheimer’s disease (ATSDR 2008aATSDR. 2008a. Public Health Statement for Aluminum. Washington, DC: Agency for Toxic Substances and Disease Registry. https://www.atsdr.cdc.gov/ToxProfiles/tp22-c1-b.pdf.
https://www.atsdr.cdc.gov/ToxProfiles/tp...
; Walton 2011Walton JR. 2011. Bioavailable aluminum: Its effects on human health. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. Amsterdam, Elsevier Academic Press. p. 315-327.). Still, the effects of daily Al consumption are yet to be determined (ATSDR 2008aATSDR. 2008a. Public Health Statement for Aluminum. Washington, DC: Agency for Toxic Substances and Disease Registry. https://www.atsdr.cdc.gov/ToxProfiles/tp22-c1-b.pdf.
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). In the United States, estimates point that an average adult ingests around 7 to 9 mg of Al every day through food, which can be contaminated in numerous ways, such as mining activity (ATSDR 2008aATSDR. 2008a. Public Health Statement for Aluminum. Washington, DC: Agency for Toxic Substances and Disease Registry. https://www.atsdr.cdc.gov/ToxProfiles/tp22-c1-b.pdf.
https://www.atsdr.cdc.gov/ToxProfiles/tp...
; Landry 2014Landry K. 2014. Human health effects of dietary aluminum. International Journal of Health Science 4: 39-45. ).

The human body is unable to use Al. On the other hand, Mn is an important element for many physiological functions in humans, such as mitochondria oxidative stress prevention, digestion, and immune response (Röllin & Nogueira 2011Röllin HB, Nogueira CMCA. 2011. Manganese: Environmental pollution and health effects. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. New York, Elsevier Academic Press. p. 229-242. ). However, when in elevated concentrations, it can cause several problems, including damage to the nervous system in prenatal stages and early childhood (Röllin & Nogueira 2011Röllin HB, Nogueira CMCA. 2011. Manganese: Environmental pollution and health effects. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. New York, Elsevier Academic Press. p. 229-242. ; Miah et al. 2020Miah MR, Ijomone OM, Okoh COA, et al. 2020. The effects of manganese overexposure on brain health. Neurochemistry international. doi: 10.1016/j.neuint.2020.104688.
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). Since Mn was the element with the highest concentration found in B. sagittalis (263.87 mg.kg-1 in unmined areas and 335.8 mg.kg-1 in mined ones), the people living near these locations, who are consuming this plant, are being subjected to a vulnerable health situation.

As Al, Ba is a non-essential metal for the human body and can be toxic on some occasions; however, the lack of known parameters for Ba contaminated food ingestion complicates the comprehension of its effects on human health (Lu et al. 2019Lu Q, Xu X, Liang L, et al. 2019. Barium concentration, phytoavailability, and risk assessment in soil-rice systems from an active barium mining region. Applied Geochemistry 106: 142-148.; Pi et al. 2019Pi X, Jin L, Li Z, et al. 2019. Association between concentrations of barium and aluminum in placental tissues and risk for orofacial clefts. Science of the Total Environment 652: 406-412. ). Studies conducted in China have shown that people who consumed rice from areas with Ba contamination presented low contamination levels (Lu et al. 2019Lu Q, Xu X, Liang L, et al. 2019. Barium concentration, phytoavailability, and risk assessment in soil-rice systems from an active barium mining region. Applied Geochemistry 106: 142-148.). This result suggests that there might be some biochemical pathways (in plants, human beings or both) that can lower Ba concentration and reduce its possible harmful effects (Lu et al. 2019Lu Q, Xu X, Liang L, et al. 2019. Barium concentration, phytoavailability, and risk assessment in soil-rice systems from an active barium mining region. Applied Geochemistry 106: 142-148.). Still, to answer this question, further investigation is required. For instance, can the consumption of leaf infusion from bioaccumulating plants grown in Ba tainted areas also present the same results?

In acidic and altered soils (product of mining activities, for example), Cd content and mobility rise, affecting soil microbiota functioning and enhancing its absorption by plants (Oti 2015Oti WO. 2015. Bioaccumulation factors and pollution indices of heavy metals in selected fruits and vegetables from a derelict mine and their associated health implications. International journal of sustainable built environment 4: 15-23. ; Feng et al. 2019Feng Y, Wang J, Bai Z, Reading L. 2019. Effects of surface coal mining and land reclamation on soil properties: A review. Earth-Science Reviews 191: 12-25. ). In the study region, soil measurements of pH ranged from 3.5 to 5.5 in mined areas and 4.5 to 6.5 in unmined ones, revealing its acidity. Indeed, high Cd concentration in soil was found (029-0.23 mg.kg-1), as well as in B. sagittalis leaves (0.25-0.30 mg.kg-1) and in consumption estimates projected considering ingestion of 2 g of B. sagittalis dry matter (Cd < 0.10 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.). Such results were observed in mined and unmined areas, possibly related to soil origin in the region, with naturally higher Cd availability (Guo et al. 2013Guo L, Lin H, Fan B, Cui X, Chen J. 2013. Impact of root water content on root biomass estimation using ground penetrating radar: Evidence from forward simulations and field controlled experiments. Plant Soil 371: 503-520.). However, high levels of Cd, already observed in rice and corn species consumed by the Chinese, may present a risk to food security, considering its harmful effects on human health, like nutrient absorption and kidney function alterations (Staessen et al. 1994Staessen JA, Amery A, Lauwerys RR, Roels HA, Ide G, Vyncke G. 1994. Renal function and historical environmental cadmium pollution from zinc smelters. Lancet 343: 1523-1537. ; Sun et al. 2008Sun Y, Zhou Q, Diao C. 2008. Effects of cadmium and arsenic on growth and metal accumulation of Cd-hyperaccumulator Solanum nigrum L. Bioresource Technology 99: 1103-1110.; Baye & Hymete 2010Baye H, Hymete A. 2010. Lead and Cadmium accumulation in medicinal plants collected from environmentally different sites. Bulletin of Environmental Contamination and Toxicology 3: 197-201. ; Ata-Ul-Karim et al. 2020Ata-Ul-Karim ST, Cang L, Wang Y, Zhou D. 2020. Effects of soil properties, nitrogen application, plant phenology, and their interactions on plant uptake of cadmium in wheat. Journal of hazardous materials 384: 121452.). Cadmium is the most abundant metal found in coal mining areas, and its high concentration is a concern for food security (Qi et al. 2014Qi Y, Huang B, Darilek JL. 2014. Effect of drying on heavy metal fraction distribution in rice paddy soil. PLOS ONE 9: 3-10. ; Zhang et al. 2015Zhang L, Mo Z, Qin J, et al. 2015. Change of water sources reduces health risks from heavy metals via ingestion of water, soil, and rice in a riverine area, South China. Science of the Total Environment 531: 163-170.).

Levels of Cu, Ni, and Zn in unmined soil were higher than in mined soil (22.13 mg.kg-1, 13.86 mg.kg-1 and 27.41 mg.kg-1, respectively). This result is possibly due to soil leaching and increased mobility in soils with a pH lower than 4.0 (Krämer & Clemens 2008Krämer U, Clemens S. 2008. Functions and homeostasis of zinc, copper, and nickel in plants. Current genetics 20: 215-271. ; Elbana & Selim 2011Elbana TA, Selim HM. 2011. Copper mobility in acidic and alkaline soils: miscible displacement experiments. Soil Science Society of America Journal 75: 2101-2110. ). Plants use Cu, Ni, and Zn for numerous metabolic activities. For example, photosynthesis and respiration require Cu, Ni is essential for the metabolic process of plant defense, and Zn is crucial to protein binding (Yruela 2005Yruela I. 2005. Copper in plants. Journal of plant physiology 17: 145-156. ; Krämer & Clemens 2008Krämer U, Clemens S. 2008. Functions and homeostasis of zinc, copper, and nickel in plants. Current genetics 20: 215-271. ; Fabiano et al. 2015Fabiano CC, Tezotto T, Favarin J, Polacco JC, Mazzafera P. 2015. Essentiality of nickel in plants: A role in plant stresses. Frontiers in Plant Science 6: 2013-2026.). As observed for plants, these metals also play a major role in human beings’ health. Copper assists in neurological formation, while Ni is crucial for proper muscular development (Plum et al. 2010Plum LM, Rink L, Hajo H. 2010. The essential toxin: Impact of zinc on human health. International Journal of Environmental Research and Public Health 7: 1342-1365. ; Bost et al. 2016Bost M, Houdart S, Oberli M, Kalonji E, Huneau JF, Margaritis I. 2016. Dietary copper and human health: Current evidence and unresolved issues. Journal of Trace Elements in Medicine and Biology 35:107-115. ). However, when at high concentrations, Cu and Ni may be toxic to humans; in fact, Cu can cause kidney diseases, and Ni can induce pulmonary fibrosis (Krämer & Clemens 2008Krämer U, Clemens S. 2008. Functions and homeostasis of zinc, copper, and nickel in plants. Current genetics 20: 215-271. ; Bost et al. 2016Bost M, Houdart S, Oberli M, Kalonji E, Huneau JF, Margaritis I. 2016. Dietary copper and human health: Current evidence and unresolved issues. Journal of Trace Elements in Medicine and Biology 35:107-115. ). Additionally, Zinc is an important metal for the immune system and has positive effects in cellular apoptosis control. Besides, it has a low intoxication rate and requires a high dosage to cause harm, such as digestive intoxication or stomach wall damage (Plum et al. 2010Plum LM, Rink L, Hajo H. 2010. The essential toxin: Impact of zinc on human health. International Journal of Environmental Research and Public Health 7: 1342-1365. ).

Even though projections for daily consumption were based on dry B. sagittalis leaves and not on its infusion, Cd and Pb presented concentrations far above the recommended levels for consumption (Cd < 0.10 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.), Pb < 1.2 x 10-3 mg.kg-1 (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
) and < 2 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.)) and should be further investigated. Just as Cd, Cr (0.57 mg.kg-1) has been found in high concentrations in mining areas and in food items grown in former coal mining areas, such as rice (Oryza spp.) in China rice plantations (Achmad & Budiawan 2017Achmad RT, Budiawan AEI. 2017. Effects of chromium on human body. Annual Research and Review in Biology 17: 1-8. ; Sun et al. 2018Sun Z, Xie X, Wang P, Hu Y, Cheng H. 2018. Heavy metal pollution caused by small-scale metal ore mining activities: A case study from a polymetallic mine in South China. Science of the Total Environment 639: 217-227. ). Cr can be found in different forms: Cr(III), Cr(IV), Cr(VI), and despite its importance for lipid and protein metabolism in humans, this metal can cause severe damage to human health, increasing chances of uterine cancer development, and causing severe respiratory symptoms (ATSDR 2008bATSDR. 2008b. Chromium (Cr) Toxicity. Atlanta, Georgia: Department of Health and Human Services Agency for Toxic Substances and Disease Registry Division of Toxicology and Environmental Medicine. https://www.atsdr.cdc.gov/csem/chromium/docs/chromium.pdf.
https://www.atsdr.cdc.gov/csem/chromium/...
; Achmad & Budiawan 2017Achmad RT, Budiawan AEI. 2017. Effects of chromium on human body. Annual Research and Review in Biology 17: 1-8. ). Considering its ability to accumulate in the food chain, added to its high absorption by plants, Cr presence in high concentrations is concerning (ATSDR 2008bATSDR. 2008b. Chromium (Cr) Toxicity. Atlanta, Georgia: Department of Health and Human Services Agency for Toxic Substances and Disease Registry Division of Toxicology and Environmental Medicine. https://www.atsdr.cdc.gov/csem/chromium/docs/chromium.pdf.
https://www.atsdr.cdc.gov/csem/chromium/...
), given that estimated levels of Cd, Cr, and Pb ingestion within 2 g of B. sagittalis infusion were already higher than recommended (Cd < 0.10 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.), Pb < 1.2 x 10-3 mg.kg-1 (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
) and < 2 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.)).

Along with that, reports on Baccharis species increasing availability in the region within the last 10-15 years also call for attention to potential growth in residents’ consumption. An increase in the Baccharis population can be related to the fact that it is a pioneer species (Heiden 2006Heiden G. 2006. Comercialização de carqueja por ervateiros da zona central de Pelotas, Rio Grande do Sul. Revista Biologia e Ciências da Terra 6: 50-57. ) that can easily develop in contaminated areas (Menezes et al.2013Menezes APS, Da Silva J, Roloff J, et al. 2013. Baccharis trimera (Less.) DC. as genotoxicity indicator of exposure to coal and emissions from a thermal power plant. Archives of Environmental Contamination and Toxicology 65: 434-441.; 2016Menezes APS, da Silva J, Fisher C, et al. 2016. Chemical and toxicological effects of medicinal Baccharis trimera extract from coal burning area. Chemosphere 146: 396-404. ). With rising numbers of abandoned and unrecovered coal mining areas in the Santa Catarina coal region (Rocha-Nicoleite et al. 2017Rocha-Nicoleite E, Overbeck GE, Müller SC. 2017. Degradation by coal mining should be priority in restoration planning. Perspectives in Ecology and Conservation 15: 202-215.; Blanco et al. 2020Blanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.a), an increase in this species availability can be expected. Consumption of B. sagittalis was reported mainly by women (i.e., 70.4 % of respondents who claimed to use this plant), which reveals women’s greater vulnerability in the region. Overall, this result acknowledges the worldwide panorama that shows that women are the most affected by contaminated environments and have a higher food security vulnerability (Lutomia et al. 2019Lutomia CK, Obare GA, Kariuki IM, Muricho GS. 2019. Determinants of gender differences in household food security perceptions in the Western and Eastern regions of Kenya. Cogent food & agriculture 5: 1694-1755.).

Food safety and human health risks related to food grown near mining areas are rather recent concerns; in China, the focus has been on Oryza spp. (rice) and Camellia sinensis (green tea), both of which may present bioaccumulative potential and be harmful to human health (Zhang et al. 2015Zhang L, Mo Z, Qin J, et al. 2015. Change of water sources reduces health risks from heavy metals via ingestion of water, soil, and rice in a riverine area, South China. Science of the Total Environment 531: 163-170.; Huang et al. 2017Huang JJ, Wei W, Cui Q, Xiei W. 2017. The prospects for China’s food security and imports: Will China starve the world via imports? Journal of Integrative Agriculture 16: 2933-2944. ; Liu et al. 2017Liu B, Ai S, Zhang W, Huang D, Zhang Y. 2017. Assessment of the bioavailability, bioaccessibility and transfer of heavy metals in the soil-grain-human systems near a mining and smelting area in NW China. Science of the Total Environment 609: 822-829.). In India, Japan, and Europe, research regarding C. sinensis bioaccumulative potential has shown that it can gather high levels of heavy metals (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.). In Canada and the United States, toxic metals from mining have been stocking up in some moose and sheep species that feed on bioaccumulating plants, being subsequently consumed by people (Schuster et al. 2011Schuster RC, Wein EE, Dickson C, Chan HM. 2011. Importance of traditional foods for the food security of two first nations communities in the Yukon, Canada. International Journal of Circumpolar Health 70: 286-300. ; Loring & Whitely 2019Loring PA, Whitely C. 2019. Food security and food system sustainability in North America. Encyclopedia Food Security Sustainability 3: 1261-133.). Research in northern Brazil has shown that the consumption of fish contaminated by gold mining activities has caused mercury to accumulate in indigenous women’s breast milk (Carvalho et al. 2009Carvalho ASC, Santos AS, Pereira SFP, Alves CN. 2009. Levels of As, Cd, Pb and Hg found in the hair from people living in Altamira, Pará, Brazil: Environmental implications in the Belo Monte area. Journal of the Brazilian Chemical Society 20: 1153-1163. ; Spurway & Soldatic 2016Spurway K, Soldatic K. 2016. “Life just keeps throwing lemons”: the lived experience of food insecurity among Aboriginal people with disabilities in the West Kimberley. Local Environment 21: 1118-1131. ).

Since these metals are invisible contaminants (without odor, taste or physical alteration) that cannot be detected by human senses (Vyner 1988Vyner HM. 1988. The psychological dimensions of health care for patients exposed to radiation and the other invisible environmental contaminants. Social Science & Medicine 27: 1097-1103.; Spurway & Soldatic 2016Spurway K, Soldatic K. 2016. “Life just keeps throwing lemons”: the lived experience of food insecurity among Aboriginal people with disabilities in the West Kimberley. Local Environment 21: 1118-1131. ), their perception by human communities is challenging (Vyner 1988Vyner HM. 1988. The psychological dimensions of health care for patients exposed to radiation and the other invisible environmental contaminants. Social Science & Medicine 27: 1097-1103.). The lack of parameters concerning food contamination by mining activity and the possible health effects resulting from their consumption only aggravates this difficulty (Vyner 1988Vyner HM. 1988. The psychological dimensions of health care for patients exposed to radiation and the other invisible environmental contaminants. Social Science & Medicine 27: 1097-1103.). Given that metal content in the human body rises at a slow rate, requiring a long period of exposure to accumulate, relating human health issues to high metal concentrations is an arduous task (Gifford 2011Gifford R. 2011. The dragons of inaction: psychological barriers that limit climate change mitigation and adaptation. American Psychologist 66: 290-302. ; Candeias et al. 2019Candeias C, Ávila P, Coelho P, Teixeira JP. 2019. Mining activities: Health impacts. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. Amsterdam, Elsevier. p. 415-435. ). Also, there is a considerable amount of diseases these metals can cause, including abdominal pain, headaches, and slowly developing cancers, increasing difficulties to diagnose diseases' sources (Vyner 1988Vyner HM. 1988. The psychological dimensions of health care for patients exposed to radiation and the other invisible environmental contaminants. Social Science & Medicine 27: 1097-1103.; Gifford 2011Gifford R. 2011. The dragons of inaction: psychological barriers that limit climate change mitigation and adaptation. American Psychologist 66: 290-302. ; Candeias et al. 2019Candeias C, Ávila P, Coelho P, Teixeira JP. 2019. Mining activities: Health impacts. In: Nriagu JO (ed.). Encyclopedia of Environmental Health. Amsterdam, Elsevier. p. 415-435. ). Altogether, these complexities make it hard for people to be aware of metal contamination and food insecurity to which they are exposed.

The impact of mining activity on edible plants is evident, yet only a few studies provide data on safe ingestion rates for humans (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.). A recent review regarding mining impacts on human health revealed that most research focuses on direct exposure to toxic agents in developed countries (Brisbois et al. 2019Brisbois BW, Reschny J, Fyfe TM, et al. 2019. Mapping research on resource extraction and health: A scoping review. Extractive Industries and Society 8: 250-259.). Still, most mining areas are in developing or undeveloped countries, but literature is scarce on food safety, especially associated to indigenous people and local communities (Vyner 1988Vyner HM. 1988. The psychological dimensions of health care for patients exposed to radiation and the other invisible environmental contaminants. Social Science & Medicine 27: 1097-1103.; Blanco et al. 2020Blanco GD, Sühs RB, Brizola E, Corrêa PF, Campos ML, Hanazaki N. 2020a. Invisible contaminants and food security in former coal mined areas of Santa Catarina, southern Brazil. Journal of Ethnobiology and Ethnomedicine 16: 1-11.a).

Baccharis is widely known and consumed in Brazil (Schripsema et al. 2019Schripsema J, Lemos MA, Dagnino D, Luna FJ. 2019. Carqueja (Baccharis sect. Caulopterae), a critical review of its history, phytochemistry and medicinal use: problems of ethnopharmacology in Latin America. Phytochemistry Reviews 18: 1181-1209. ), but its traditional consumption is also frequently reported in Uruguay (Abad & Bermejo 2007Abad MJ, Bermejo P. 2007. Baccharis (compositae): A review update. Arkivoc 2007: 76-96.), Argentina (Abad & Bermejo 2007Abad MJ, Bermejo P. 2007. Baccharis (compositae): A review update. Arkivoc 2007: 76-96.), Chile (Morales et al. 2008Morales G, Paredes A, Sierra P, Loyola LA. 2008. Antimicrobial activity of three Baccharis species used in the traditional medicine of Northern Chile. Molecules 13: 790-794. ), Colombia (Abad & Bermejo 2007Abad MJ, Bermejo P. 2007. Baccharis (compositae): A review update. Arkivoc 2007: 76-96.), Mexico (Abad & Bermejo 2007Abad MJ, Bermejo P. 2007. Baccharis (compositae): A review update. Arkivoc 2007: 76-96.), United States (Haque et al. 2008Haque N, Peralta-Videa JR, Jones GL, Gill TE, Gardea-Torresdey JL. 2008. Screening the phytoremediation potential of desert broom (Baccharis sarothroides Gray) growing on mine tailings in Arizona, USA. Environment Pollution 153: 362-378. ), and Canada (Freire et al. 2007Freire SE, Urtubey E, Giuliano DA. 2007. Caracteres epidérmicos de las especies del género Baccharis (Asteraceae) usadas en la medicina popular. Caldasia 29: 23-38. ). Likewise, Baccharis occurrence, as well as its heavy metal bioaccumulation have been reported in mining areas (Carreira 2007Carreira RC. 2007. Baccharis trimera (Less.) DC. (Asteraceae): estudo comparativo dos óleos voláteis, atividade biológica e crescimento de estacas de populações ocorrentes em áreas de Cerrado e Mata Atlântica. PhD Thesis, São Paulo University, São Paulo.; Haque et al. 2008Haque N, Peralta-Videa JR, Jones GL, Gill TE, Gardea-Torresdey JL. 2008. Screening the phytoremediation potential of desert broom (Baccharis sarothroides Gray) growing on mine tailings in Arizona, USA. Environment Pollution 153: 362-378. ; Oti 2015Oti WO. 2015. Bioaccumulation factors and pollution indices of heavy metals in selected fruits and vegetables from a derelict mine and their associated health implications. International journal of sustainable built environment 4: 15-23. ). For instance, in the United States, Pb absorption and translocation to leaves of another species of the genus Baccharis (B. sarothroides) were observed (Haqueet al. 2008Haque N, Peralta-Videa JR, Jones GL, Gill TE, Gardea-Torresdey JL. 2008. Screening the phytoremediation potential of desert broom (Baccharis sarothroides Gray) growing on mine tailings in Arizona, USA. Environment Pollution 153: 362-378. ). In 2020, medicinal plants use had a significant increase worldwide since the COVID-19 pandemic caused people to turn to medicinal plants more than in the former period (Nugraha et al. 2020Nugraha RV, Ridwansyah H, Ghozali M, Khairani AF, Atik N. 2020. Traditional herbal medicine candidates as complementary treatments for COVID-19: A review of their mechanisms, pros and cons. Evidence-Based Complementary and Alternative Medicine: 1-12. ).

All described situations increase food insecurity and human health vulnerability in traditional and local communities that live close to mining areas and contaminated environments. A study limitation was that, since the analyzed plants were not in a controlled environment, it was not possible to determine metals’ original soil concentrations and compare them to the values absorbed by the plant. However, Cd and Pb levels (0.25-0.3 mg.kg-1 and 3.8-4 mg.kg-1) were above the reference levels (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
; Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.; Westman 2018Westman W. 2018. China releases the standard for maximum levels of contaminants. Beijing, China: China Food and Drug Administration. https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=China%20Releases%20the%20Standard%20for%20Levels%20of%20Contaminants%20in%20Foods%20_Beijing_China%20-%20Peoples%20Republic%20of_5-9-2018.pdf.
https://apps.fas.usda.gov/newgainapi/api...
) in plants from both mined and unmined areas. Additionally, Cd and Pb estimate consumption (Cd < 0.10 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.), Pb < 1.2 x 10-3 mg.kg-1 (ANVISA 2013ANVISA. 2013. Resolução RDC no 42, de 29 de agosto de 2013. Agência Nacional de Vigilância Sanitária. https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2013/rdc0042_29_08_2013.html. 07 Jul. 2021.
https://bvsms.saude.gov.br/bvs/saudelegi...
) and < 2 x 10-3 mg.kg-1 (Soliman 2016Soliman N. 2016. Metals Contents in black tea and evaluation of potential human health risks to consumers. Health Economics and Outcome Research 2: 2-5.), are higher than recommended. Thus, B. sagittalis medicinal consumption in this area is not safe, as it poses a threat to food security and local communities’ health.

Conclusion

Studies on food and medicinal plants contamination through mining activities are scarce and require greater attention. This study results revealed contamination in a plant of native occurrence in mined areas and in surrounding areas without mining activity, which is traditionally used as medicine. High levels of Al, Cd, Mn, and Pb were observed in B. sagittalis, showing that collecting this species from mined regions for consumption is not safe. It also adds concerns regarding the lack of knowledge on safe consumption levels of contaminated plants. The importance of studies like this must be highlighted, since they are crucial to provide a better understanding of mining impacts on food security and human health of populations living close to mined regions.

Acknowledgments

The authors would like to thank Maiara Hayata, Patricia Figueredo, Daniele Cantelli, Maiara Gonçalves, Helen Assis, Bianca Minink, Escarlet Brizola, Brisa Marciniak, and colleagues from the Soil and Limestone Chemical Analysis laboratory in the collection and preparation of the material for analysis. The authors are grateful for the funding in part by the Higher Education Personnel Improvement Coordination, Brazil (CAPES) - Finance Code 001, and GDB doctoral grant. Thanks to CNPq for NH research productivity scholarship (309613/2015-9, 304515/2019-1).

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Publication Dates

  • Publication in this collection
    10 Oct 2022
  • Date of issue
    2022

History

  • Received
    10 Nov 2021
  • Accepted
    15 June 2022
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