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Bioarchaeology of Arsenic, an Invisible Natural Pollutant, and Its Effect on the Mitimaes of Camarones Cove, Arica, during Inca Times

Published online by Cambridge University Press:  21 October 2022

Bernardo Arriaza*
Affiliation:
Instituto de Alta Investigación, Universidad de Tarapacá, Arica, Chile
Vivien G. Standen
Affiliation:
Departamento de Antropología, Facultad de Ciencias Sociales y Jurídicas, Universidad de Tarapacá, Arica, Chile
Leonardo Figueroa
Affiliation:
Departamento de Química, Facultad de Ciencias, Universidad de Tarapacá, Arica, Chile.
*
([email protected], corresponding author)
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Abstract

During the expansion of Tawantinsuyo, the Inca Empire sustained its hegemony by using multiple strategies, including moving specialized groups called mitimaes to their conquered territories. This study examines bioarchaeological evidence from the Camarones 9 (CAM-9) Inca period cemetery at the mouth of the Camarones Valley in northern Chile. The waters in this valley contain concentrations of arsenic that are 100 times above the norm (10 μg/L) for human ingestion, causing serious health consequences. We study the environmental health effects on this population, using atomic absorption spectrometry and hydride generation to investigate arsenic concentration in the bone tissues of 16 individuals sampled from this burial site. Three of four individuals presented arsenic levels in their bones that were beyond the standard 1 μg/g, with a median of 3.6 μg/g; in some, the levels were nine times higher than those currently recommended by the World Health Organization. Considering previous and current bioarchaeological evidence, especially the high arsenic levels found in these individuals, we postulate that the CAM-9 site population corresponds to mitimaes who settled on the Camarones coast. This study is relevant to all regions of the world that present ecotoxic loads.

Durante la expansión del Tawantinsuyo, el Imperio Inca mantuvo su hegemonía a través de múltiples estrategias, incluyendo el traslado de grupos especializados, llamados mitimaes, a sus territorios conquistados. Se discuten las evidencias bioarqueológicas provenientes del cementerio Camarones 9 (CAM-9), en la desembocadura del valle de Camarones, norte de Chile, asociado al periodo Inca. Las aguas de este valle presentan concentraciones de arsénico 100 veces por sobre la norma (10 μg/L), lo que genera consecuencias nocivas para la salud. Mediante espectrometría de absorción atómica con generación de hidruros, se estudiaron las concentraciones de arsénico presente en los tejidos óseos de16 individuos de CAM-9. Tres de cada cuatro individuos presentaron niveles de arsénico en sus huesos más allá de la norma de 1 μg/g, con una mediana de 3,6 μg/g, y algunos con concentraciones nueve veces mayor a lo recomendado por la Organización Mundial de la Salud. A la luz de los estudios bioarqueológicos previos y actuales, en particular por el alto nivel de arsénico presente en los individuos, se postula que la población inhumada en CAM-9 correspondería a mitimaes asentados en la costa de Camarones. Este estudio es relevante para otras regiones del mundo que presentan importantes cargas eco-tóxicas.

Type
Article
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of the Society for American Archaeology

All environments contain hidden hazards to humans. When a population moves to an allochthonous place either by choice or by force, it faces the challenge of adapting to a new ecological niche. Thus, understanding the environment's role in the biocultural evolution and health consequences of ancient population mobility is of paramount importance.

During the expansion of Tawantisuyo, the Incas occupied a variety of macro-ecological zones, from jungles to the vast and inhospitable Atacama Desert, the focus of this study. To help impose, maintain, expand, and consolidate the empire's ideology; transmit their way of life, cultivation methods, and strategies; and gain tribute for the state, among other activities, the Inca rulers not only mobilized their armies but also moved entire communities, called mitimaes or mitmaqkuna, to very distant places (Horta Reference Horta2015; Noack Reference Noack2018). Some groups were displaced from their native regions as punishment for opposing the Inca. In the Quechua language, mitmaqkuna means “upstart man” or “settled in a place different from his place of origin” (González-Holguín Reference González-Holguín1952 [1608]:140). The mitimaes fulfilled strategic military, sociocultural, and religious functions, depending on the empire's needs. For instance, they were tasked with spreading the Quechua language and customs or taking care of the huacas (shrines) and important sanctuaries. Productive mitimaes were charged with incentivizing, improving, or producing goods for the state (Horta Reference Horta2015; Murra Reference Murra1972; Noack Reference Noack2018). Although mitimaes may have been dependent on a curaca (chief), ultimately they functioned exclusively for the benefit of the Inca state (Noack Reference Noack2018).

Thus, various populations of mitimaes were relocated to places far away from Cusco or their ancestral locations. Forced to experience this diaspora, the populations had to carry out the activities entrusted to them by the Inca while adapting to the challenges in their new ecological and geographic environment. In this article, we ask whether bioarchaeological evidence of mitimaes can be found in extreme northern Chile. If so, what was their primary role, and how did the new environment affect their health and productivity?

One of the challenges faced by new arrivals to extreme northern Chile would have been water poisoning caused by the high amount of arsenic present in local rivers (Álvarez Reference Álvarez2014; Arriaza, Amarasiriwardena, et al. Reference Arriaza, Huaman, Villanueva, Tornero and Aravena2018; Arenas Reference Arenas H.2016; Bundschuh et al. Reference Bundschuh, Nicolli, Blanco, Blarasin, Farías, Cumbal, Cornejo, Bundschuh, Carrera and Litter2008; Figueroa Reference Figueroa2001), which led to a condition known as chronic regional endemic hydroarsenicism (CREHA; Litter and Bundschuh Reference Litter and Bundschuh2010). The Atacama Desert is rich in minerals that, when mixed with water, are incorporated into the food chain and eventually consumed by humans, causing severe health problems (Hopenhayn et al. Reference Hopenhayn, Ferreccio, Browning, Huang, Peralta, Gibb and Hertz-Picciotto2003; Hopenhayn-Rich et al. Reference Hopenhayn-Rich, Browning, Hertz-Picciotto, Ferreccio, Peralta and Gibb2000; Tondel et al. Reference Tondel, Rahman, Magnuson, Chowdhury, Faruquee and Ahmad1999). Therefore, the ancient populations that settled in these places, particularly those who relocated to them, very likely suffered from water poisoning, the effects of which ranged from stomachaches to various types of cancer.

Since ancient times, poisoning by natural polycontaminants (e.g., arsenic, boron, and lithium) has occurred through the ingestion of water or of contaminated products (e.g., plants, animals) that consume the same water sources, thereby incorporating these invisible polycontaminants into their food chain (Arriaza et al. Reference Arriaza, Dulasiri Amarasiriwardena, Vivien Standen, Bartkus and Bandak2010; Byrne et al. Reference Byrne, Amarasiriwardena, Bandak, Bartkus, Kane, Jones, Yáñez, Arriaza and Cornejo2010; Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988; Swift et al. Reference Swift, Cupper, Greig, Westaway, Carter, Santoro, Wood, Jacobsen and Bertuch2015). Of these elements, arsenic is the most toxic, and its levels in water sources vary regionally. Water in the Camarones River reaches an annual arsenic (As) average of 1,000 μg/L. Thus, considering the endemic nature of this contamination, arseniasis would have affected the daily lives of those who had not been previously exposed or who were more susceptible to this toxic element, exacting a toll on their subsistence and health. If mitimaes were relocated to Camarones, they would have been exposed to the health risk of arsenic poisoning.

It should be noted that mitimaes populations retained their ethnic origins, kinship ties, ancestral customs, clothing, and headdresses while holding economic obligations to their curacas (Horta Reference Horta2015; Noack Reference Noack2018). Maintaining their identity served to make them identifiable by the authorities and differentiated them from the locals, making them discoverable in the bioarchaeological record. This is especially true in places such as the Atacama Desert, where the excellent preservation of bioarchaeological remains has facilitated the study of grave goods and deceased individuals.

The coexistence of multiethnic groups in territories in northern Chile during the Late Intermediate period (ca. AD 1000–1450) has been postulated based on ethnographic and archaeological records (Hidalgo Reference Hidalgo and Hidalgo2004; Hidalgo and Focacci Reference Hidalgo and Focacci1986). Rostworowski de Diez Canseco (Reference Rostworowski de Diez Canseco1986:129; translation by the authors) notes, “During the Late Horizon, in each of the valleys within the Colesuyu area, there were innumerable curacazgos of diverse extensions. . . . Based on archival information, the main fishermen settlements in Moquegua, Tacna, Arica, and south Atacama were established on the coast and at the mouth of rivers, forming particular villages led by their own chiefs.”

The influence of the Inca state during the Late Horizon (ca. AD 1450–1550) and the evidence of new populations in the extreme north of Chile are revealed there by the network of roads (capac ñan), resting places (tambos), storage deposits (colcas), and administrative and housing centers; for example, at sites AZ-15 and Saguara (Santoro and Muñoz Reference Santoro and Muñoz1981; Schiappacasse and Niemeyer Reference Schiappacasse and Niemeyer1989, Reference Schiappacasse and Niemeyer2002) and at cemeteries such as Chaca 5 and PLM-6 (Horta Reference Horta2000, Reference Horta2011a, Reference Horta2015). The AZ-15 village and Chaca 5 cemetery provide evidence for foreign populations that moved to the Azapa and Vitor Valleys, respectively, during the Inca period.

Other sites with similar ceramic and cultural characteristics include PLM-6 (on the Arica coast), where radiocarbon dates of hair combs from this site range from the Late period (cal AD 1520–1570) to Spanish contact (Arriaza et al. Reference Arriaza, Standen, Heukelbach, Cassman and Olivares2014). CAM-9 (a coastal site at Camarones Cove), although with fewer goods, is also associated with the Inca period (Horta Reference Horta2011a, Reference Horta2011b, Reference Horta2015; Santoro et al. Reference Santoro, Romero, Standen, Valenzuela and Topic2009). Based on this evidence, the populations of these sites correspond to Altiplanic colonies that settled in different ecological zones, including the lowland and coastal valleys. In contrast, Cassman (Reference Cassman2000), who studied Arica textiles from the AZ-140 and AZ-71 valley sites, as well as the PLM-9 coastal sites, which range from AD 900 to 1400, argues that mortuary textiles did not support a multiethnic hypothesis for these sites and that many textiles were frequently repaired.

Murra (Reference Murra1972) suggests that different ethnic groups exploited different ecological areas to locate complementary resources; however, the available water quality must have constrained their quality of life and the volume of resources produced. Proving the existence of multiethnic groups or even of a foreign group is a challenge, particularly if they vary regionally across time and space. In this sense, if nonlocal groups were present in the Arica area, then it is worth investigating how they were affected by the local environment.

Yet, different lines of evidence suggest the presence of nonlocal populations in various Andean regions, including northern Chile during the Inca Horizon. Such evidence raises several questions: What kind of foreign populations (e.g., military or productive) would be present in the archaeological record? What is the bioanthropological evidence? And how were these displaced populations affected when they faced new ecological niches? Undoubtedly, the first generation of relocated populations suffered greatly after leaving behind their natural habitat, food, families, and customs. This was no minor problem, considering that individuals and populations faced different potential risks in each environment, some of which were visible and others invisible to the human eye, such as water poisoning. Exposure to environmental stressors present in new niches is an important factor that affects daily life, as well as economic and social activities (Bigham and Lee Reference Bigham and Lee2014). Of these challenges in northern Chile, water quality is the most serious stressor and needs to be examined when discussing ancient health and socioeconomic dimensions of Andean populations that settled in allochthonous places.

Before relocating, ancestral populations had likely already experienced an adaptation process in their original environments. In some of the environments where the Inca relocated new populations, they unknowingly were exposed to arsenic-laden water. In this study, we both summarize previous publications regarding arseniasis in the CAM-9 population and provide new analytical arsenic data for this site, proposing that CAM-9 represents a nonlocal population. We integrate archaeological and bioarchaeological data to (1) deepen understanding of the environment's role in the biocultural evolution of translocated populations to new ecological niches, (2) investigate how the new environment could have affected the productivity level of the relocated populations, and (3) shed light on adaptation processes experienced by different human groups in the past that faced hidden natural contaminants such as arsenic.

Study Background

Natural Environmental Pollution

The waters in northern Chile contain very high levels of natural contaminants (Bundschuh et al. Reference Bundschuh, Nicolli, Blanco, Blarasin, Farías, Cumbal, Cornejo, Bundschuh, Carrera and Litter2008; Echeverría et al. Reference Echeverría, Niemeyer, Muñoz and Uribe2018; Figueroa Reference Figueroa2001; Yáñez et al. Reference Yáñez, Mansilla, Paola Santander, Fierro, Cornejo, Barnes and Amarasiriwardena2015). Arsenic (As), boron (B), and lithium (Li) are found at concentrations that exceed 10–100 times the standard concentrations recommended by the World Health Organization (WHO) for human consumption. Of these three eco-pollutants, As is the most harmful to humans. It is found in both surface water and groundwater, and its concentration varies depending on the geographic area. For example, the waters in the San José River (Azapa) are of better quality than those in the Lluta and Camarones Rivers (Figueroa Reference Figueroa2001). In some places, such as Quebrada de Camarones, As concentrations average 1,000 μg/L—one hundred times more than the standard limit proposed by the WHO, which recommends that As in drinking water should not exceed 10 μg/L (Bundschuh et al. Reference Bundschuh, Nicolli, Blanco, Blarasin, Farías, Cumbal, Cornejo, Bundschuh, Carrera and Litter2008; Figueroa Reference Figueroa2001; WHO Reference WHO2003, Reference WHO2008). Chronic regional endemic hydroarsenicism affects many populations (Litter and Bundschuh Reference Litter and Bundschuh2010) and presents a mosaic-type spatial distribution; that is, nearby communities can have different levels of natural contamination (Arriaza, Amarasiriwardena, et al. Reference Arriaza, Amarasiriwardena, Standen, Yáñez, Van Hoesen and Figueroa2018; Swift et al. Reference Swift, Cupper, Greig, Westaway, Carter, Santoro, Wood, Jacobsen and Bertuch2015). Therefore, water quality is of utmost importance when discussing the possible paleopathological, epidemiological, dietary, and social dynamics that confronted the ancient populations in this arid area of the continent. Álvarez (Reference Álvarez2014) postulates that the Incas preferred rivers with brackish water, because the abundance of water year-round allowed for better management of their maize crops in the Locumba, Sama, Lluta, Camarones, and Loa Valleys. The arsenic water in Lluta and Camarones presented a great health risk when consumed on a recurrent basis.

Several epidemiological studies have demonstrated that the deterioration of individual health in As-contaminated environments is directly proportional to the As concentration in the water, years of continuous exposure, accumulation in the individual, and age of the individual (Ahmad et al. Reference Ahmad, Salim Sayed, Barua, Khan, Faruquee, Jalil, Abdul Hadi and Talukder2001; Bundschuh et al. Reference Bundschuh, Nicolli, Blanco, Blarasin, Farías, Cumbal, Cornejo, Bundschuh, Carrera and Litter2008; Castro de Esparza Reference de Esparza and Luisa2004; Figueroa Reference Figueroa2001; Hopenhayn et al. Reference Hopenhayn, Ferreccio, Browning, Huang, Peralta, Gibb and Hertz-Picciotto2003; McClintock et al. Reference McClintock, Chen, Bundschuh, Oliver, Navoni, Olmos, Lepori, Ahsan and Parvez2012; Tondel et al. Reference Tondel, Rahman, Magnuson, Chowdhury, Faruquee and Ahmad1999; WHO Reference WHO2003, Reference WHO2008). Epidemiological studies also indicate that CREHA causes acute and chronic health problems, such as retarded growth and development in children, skin lesions, increased perinatal and infant mortality, congenital anomalies, and several types of cancer (Hopenhayn et al. Reference Hopenhayn, Ferreccio, Browning, Huang, Peralta, Gibb and Hertz-Picciotto2003; Hopenhayn-Rich et al. Reference Hopenhayn-Rich, Browning, Hertz-Picciotto, Ferreccio, Peralta and Gibb2000; Tondel et al. Reference Tondel, Rahman, Magnuson, Chowdhury, Faruquee and Ahmad1999).

The As in water originates from geomorphology and volcanoes in the area. After mixing with water, it cannot be easily perceived, because it is colorless, odorless, and tasteless; that is, it is invisible to the senses. Studies of populations that inhabited the Atacama Desert must consider such contamination, especially considering the poor water quality in the water sources (Figueroa Reference Figueroa2001), the limited number of rivers (which have a low flow that concentrates minerals), and the paucity of other water sources (wells and springs) available. The first populations that explored prehistoric regions sporadically (those with rotational mobility) and those that settled permanently must have adapted to harsh living conditions in an environment with scarce water sources, which were not always of good quality. We are what we consume; therefore, studying the presence of chronic arsenic poisoning in ancient populations is important in determining the effects of prolonged exposure to endemic contaminants (Figure 1).

Figure 1. General diagram of overexposure to arsenic.

The CAM- 9 Site

The CAM-9 site is located approximately 100 km south of Arica City in the Quebrada de Camarones. It is situated on the periphery (to the southeast) of a large shell deposit, located on the southern terrace of the ravine and adjacent to CAM-8, a Late Intermediate period site (ca. AD 1400), and to CAM-14 and CAM-17, both Archaic sites. The CAM-9 site is contiguous to the coast and the mouth of the Camarones River, where its ancient inhabitants could plant crops, consume river water, and supplement their subsistence with extractions from nearby coastal resources (Figures 2 and 3). Although plants are good arsenic bioaccumulators (Ruiz and Amienta Reference Ruiz and Armienta2012), it is likely that the daily amount of arsenical water ingested significantly outweighed the quantity of arsenic ingested per day from plant or animal foods. Yet, the consumption of edible plants irrigated with arsenical water was likely another source of arsenic contamination (Arriaza et al. Reference Arriaza, Dulasiri Amarasiriwardena, Vivien Standen, Bartkus and Bandak2010; Cornejo et al. Reference Cornejo, Lienqueo, Arriaza, Acarapi and Arenas2008).

Figure 2. Map illustrating the location of the archaeological sites mentioned.

Figure 3. Surrounding area of CAM-9 site and terrace, showing the fertility of the river delta (photograph by Carlos Chow). (Color online)

Dating to the Inca period, the CAM-9 site shows evidence of a mixed economy, which included hunting, fishing, and gathering; growing crops, including maize; and using farming tools. Vessels in the form of bowls and aryballoi were also found at the site (Muñoz Reference Muñoz1989; Schiappacasse and Niemeyer Reference Schiappacasse and Niemeyer1989). Radiocarbon dates place the site between AD 1320 and 1680 (Catalán Reference Catalán2008; Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988; Table 1). According to Muñoz (Reference Muñoz1989:103), an Altiplanic influence is suggested by the ceramics found at CAM-9, which were similar to the chilpe and saxamar styles. Based on radiocarbon dates, this pottery was attributed to the highland valleys of Arica and Camarones between AD 1220 and 1400. He suggests that there was interaction between coastal groups and Altiplanic populations, as well as an Inca population dedicated to agricultural and maritime exploitation, in CAM-9.

Table 1. Radiocarbon Dates of the CAM-9 Site.

CAM-9 has been excavated twice. It was excavated in the early 1960s by a team from the Regional Museum of Arica (led by Percy Dauelsberg), who excavated the majority of the funerary contexts, leaving the bodies in situ. In 1985, Percy Dauelsberg and Vivien Standen of the University of Tarapacá excavated the site again, recovering bodies that had been left in situ and other contexts that had not been disturbed. They uncovered 41 tombs, located in pits with individual burials (Carmona Reference Carmona2004). Of these individuals, 20 were male, 7 were female, and in 14 cases, sex was undetermined (Muñoz Reference Muñoz1989). The most frequent offerings were hunting and fishing artifacts (e.g., harpoons and lithic weights), textiles (wool bags), food remains, and symbolic ritual objects.

The Inca tombs found at the CAM-9 site resembled circular or oval pits whose diameters ranged from 30 to 90 cm, with some exceeding 100 cm. The bodies were adorned with thick braids, some in the form of a set of small braids at the back of their heads and others with lateral braids. The bodies were placed in a squatting position and then wrapped from head to toe in bichrome camelid wool blankets (brown with some striped decorations on both sides) to form a burial bundle (Figure 4). The bundles were buried at a depth of 40–80 cm. In this period, the bodies and bundles were always painted red, the blankets had red lateral stripes, and some elements of the offering that accompanied the deceased were also painted red (Ulloa et al. Reference Ulloa, Standen and Gavilán2000). A headdress (Figure 5), possibly made with Otaria sp. filaments (fastened with wool at its base) or with seabird feathers, was placed at the head level. Some of these headdresses were accompanied by a row of projectile points. In other cases, cephalic ornaments were simpler, and wool yarn was placed as a headband.

Figure 4. Complete undisturbed tomb, with its grave goods (harpoons, shafts, bags, and a vessel) and cephalic headdress possibly made of Otaria sp. filaments (CAM-9 Tomb 11) (photograph by Vivien Standen). (Color online)

Figure 5. Detail of headdress made of possible Otaria sp. filaments (CAM-9 Tomb 11) (photograph by Vivien Standen). (Color online)

Horta (Reference Horta2015:390) stated that CAM-9 was a camanchaca (coastal fishing) population: “regarding the aforementioned cemeteries for the relocated population, I have concluded that, on the contrary, the population of Playa Miller 6 and Camarones 9 would have been camanchacas and would have survived as transculturated camanchacas until posthispanic times” (translation by the authors). She also argued that the main activity they engaged in was hunting sea lions and cetaceans (Horta Reference Horta2015:334).

Previous Bioanthropological Studies in CAM-9

Figueroa and colleagues (Reference Figueroa, Razmilic, Allison and González1988) reported on 31 unbundled and autopsied bodies from Camarones to quantify the degree of As intoxication in various tissues (mainly soft). They found that 84% of the bodies exhibited skin lesions and that the analyzed organs far exceeded the As intake values established as normal, finding values that were 342 (kidneys), 113 (liver), 44 (skin), 34.4 (hair), 29.3 (nails), and 13 times (bones) the recommended norm. This concentration of As retained in different body tissues indicates that the ancient inhabitants of CAM-9 consumed high levels of As, especially from geologically contaminated water. They found that skin lesions correlated positively with age: the older the individual, the higher the number of skin lesions present. In contrast, studies focusing on the skin of individuals from Azapa archaeological sites, such as AZ-14 (N = 13), AZ-71 (N = 12), and AZ-140 (N = 19), did not exhibit signs of hyperkeratosis or skin lesions that could be associated with arseniasis (Arriaza Reference Arriaza2021).

Another study found that individuals from CAM-9 had a significantly higher frequency of spina bifida occulta in the sacrum—a defect of multifactorial and environmental origin associated with the interruption of the neural tube closure—than did the ancient populations of Arica (Lluta 54 and Azapa 140 sites combined) with values of 13.5% and 2.4%, respectively (Silva et al. Reference Silva, Arriaza and Standen2010). The CAM-9 population had spina bifida occulta values that were nearly six times higher than those of the Lluta and Arica Valleys; this reflected greater environmental stress, because inorganic As crosses the placental barrier and directly causes the development of congenital malformations, such as spina bifida. In addition, studies of As levels in the hair of mummies from Atacama in northern Chile, using laser ablation mass spectrometry, revealed that these levels were much higher in the coastal populations than in the valleys (Arriaza et al. Reference Arriaza, Dulasiri Amarasiriwardena, Vivien Standen, Bartkus and Bandak2010). Of the four CAM-9 individuals reported, all had values greater than 1 μg/g (the norm for hair), and two reached levels around 27 and 47 times this value. From a comparative regional perspective, Echeverría and colleagues (Reference Echeverría, Niemeyer, Muñoz and Uribe2018) quantified As in hair (AsH) from the agroceramic period of northern Chile (Pica-8, Topater, and San Pedro de Atacama). They found significant differences in AsH between groups but no clear association with water sources. Interestingly a few individuals from Pica-8 and Topater presented extremely high AsH values. Echeverría and coauthors (Reference Echeverría, Niemeyer, Muñoz and Uribe2018) argued that they were nonlocal individuals who had presumably used rich As resources. In addition, Swift and colleagues (Reference Swift, Cupper, Greig, Westaway, Carter, Santoro, Wood, Jacobsen and Bertuch2015) reported on 21 precontact skeletal coastal samples from Caleta Vitor (about 52 km north of Camarones) that presented 33% arseniasis (>1 ppm), demonstrating the continuing risk of arsenic poisoning over several millennia of occupation at one site (ca. 3900–500 cal BP). Even though their sample size was small, Swift and colleagues (Reference Swift, Cupper, Greig, Westaway, Carter, Santoro, Wood, Jacobsen and Bertuch2015) stated that Tiwanaku through to Inca cases presented much higher As concentrations values (mean of 2.736 ppm).

At CAM-9, other bioarchaeological data indicate that the site had a mixed economy (Arriaza, Huaman, et al. Reference Arriaza, Amarasiriwardena, Standen, Yáñez, Van Hoesen and Figueroa2018). Analysis of dentition revealed a high percentage of caries, dental calculus, and plant consumption (e.g., Zea mays, Phaseolous sp., among others). In addition, paleopathological studies of 17 skulls of CAM-9 children revealed that 65% had mild to moderate crib lesions (Brito Reference Brito2020), reflecting health problems that were most likely products of anemia and poor water quality. Analysis of the presence of bony growth in the ear canals (external auditory exostosis) in 58.3% (7 of 12) of the CAM-9 cases suggests the intensive practice of maritime activities. In addition, these auditory exostoses are larger than those of individuals in other coastal populations in the region, most likely reflecting the continuous exploitation of coastal resources (Standen et al. Reference Standen, Arriaza and Santoro1997).

Thus, various studies conducted on the CAM-9 population reveal the presence of pathology associated with a high concentration of arsenic. However, these analyses do not delve into the characteristics of this population or the causes of their arsenicism. Our study provides new analytical data arguing that the CAM-9 population is a foreign group and therefore susceptible to arsenic.

Materials and Methods

Bioarchaeological Sample

To contextualize the archaeological samples, we reviewed archival records of the Museo Arqueológico de la Universidad de Tarapacá in San Miguel de Azapa (MASMA) and related published papers (e.g., Figueroa Reference Figueroa2001; Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988). MASMA also houses the skeletons and soft tissue of many of the mummies autopsied during the 1980s. In this study, we sampled 16 of these skeletal remains for chemical analysis. We knew the sex of most of these remains because the external sex organs remained intact. When soft tissue was not present, we estimated their sex using standard protocols for pelvic and cranial characteristics (Buikstra and Ubelaker Reference Buikstra and Ubelaker1994). Eleven individuals were female, and five were males. Age was determined by observing the stage of development of dental eruption and bone growth (e.g., epiphyseal fusion stages) and by using standard scoring of the pubic symphysis (Brooks and Suchey Reference Brooks and Suchey1990) for younger people and the auricular surface for adults (Lovejoy et al. Reference Lovejoy, Meindl, Pryzbeck and Mensforth1985). Following Buikstra and Ubelaker (Reference Buikstra and Ubelaker1994), we grouped the 16 individuals into these age categories: four were adolescents (12–20 years), three were young adults (20–35 years), seven were middle adults (35–50 years), and two were older adults (50+ years).

Diagenesis

Previous studies using ancient samples from the Atacama Desert indicate that diagenetic contamination is absent or minimal in mummy tissues due to the absence of rain (Byrne et al. Reference Byrne, Amarasiriwardena, Bandak, Bartkus, Kane, Jones, Yáñez, Arriaza and Cornejo2010; Kakoulli et al. Reference Kakoulli, Prikhodko, Fischer, Cilluffo, Uribe, Bechtel, Fakra and Marcus2014); the clothing and wrappings of Andean mummies also protected buried bodies from harsh environments. The mummy bundles in CAM-9 were found on the dry sand slopes of the Atacama Desert, away from the local shallow rivers. The Camarones River is seasonal, exoreic, and has a low annual flow; for example, in 2018 it had a water flow of 1.0 m3/s (DGA 2019). Therefore, it likely did not affect this archaeological site or its remains. In addition, the prevalence of salts in the soil of the region prevents the proliferation of microorganisms that degrade collagen, thus contributing to keeping the bone matrix of bioarchaeological samples intact (Barrientos et al. Reference Barrientos, Sarmiento and Galligani2016) and allowing various archaeometric studies to be conducted.

Chemical Analysis of the Bioanthropological Samples

We followed protocols of the analytical chemistry laboratory at the Universidad de Tarapacá in Arica to analyze the samples.

First, each sample was cleaned mechanically and with a no. 21 sterile scalpel, and all external organic and inorganic material present in the remains of the ribs sampled were removed. A minimum of 1 g of clean bone sample was obtained. Second, clean bone pieces for each sample were fragmented and reduced to <0.5 mm particle sizes in an analytically clean and dry porcelain mortar. They were then stored in clean, dry, and sealed bottles with identification labels.

Third, the ground rib bone samples were subjected to chemical dissolution. Chemical digestion, in a mixture of acids (nitric and hydrochloric), allows the solubilization of minerals, such as apatite, hydroxyapatite, and fluorapatite, and the larger fraction of the bone. The acid mixture facilitates the release and transformation of As from the bone to a chemical compound, such as the acid arsenate anion, H2AsO4-; this is an arsenical chemical species that is soluble in the aqueous and acid medium, representing, to a maximum degree, the total As present in the rib bone.

In a 100 mL Pyrex beaker, 1 g ± 1 × 10–4 g of the ground rib bone sample was weighed, to which we added 5 mL of fuming hydrochloric acid 37% (w/w) for analysis of EMSURE® ACS, ISO, and REAG. Ph Eur; we then added 2 mL of nitric acid 65% (w/w) for analysis of EMSURE® ISO. This heterogeneous mixture was placed in a vessel covered with a convex Teflon plate, 70 mm in diameter. It was heated on a heating plate in a semi-closed system until the solid material was boiling and totally dissolved and the organic matter obtained partial oxidation. This process was completed when NOx gas, which is brownish in color, was emitted.

The resulting solution was diluted in a beaker, using 10 mL of demineralized water, free of As, and then brought to a slow boil again for two to three minutes. It was then allowed to cool to 20°C–21°C, and the solution was subsequently increased to 25 mL using demineralized water. The resulting solution was then homogenized, filtered through ADVANTEC 5 B quantitative ash-free filter paper with a diameter of 110 mm, placed over a Pyrex analytical funnel, and transferred to a hermetically sealed and properly identified polypropylene bottle. The digested sample was used in this state for As quantification.

At this stage, the As concentration in the rib sample solution, which contained the original As in the transformed sample, was measured using the arsenamine hydride (AsH3) gas-generation methodology, and calculated by the stoichiometry of the respective chemical reaction. For this purpose, we used a continuous transport system of arsenic gas that was connected first to the quantification instrument (atomic absorption spectrophotometer with hydride generation, EAA/GH) and then to an atomization system in a quartz cell heated with an air and acetylene flame. The instrument's software, which was calibrated using standards of known As concentrations, enabled us to obtain calibration parameters that established the degrees of precision and sensitivity of the measurement, as well as the As concentration data in the observed or measured solution. The concentration data obtained from each sample are related to the quantitative data from the digestion solution achieved and the mass of the initial solid sample. The As concentration in the rib sample was thus obtained, which can be expressed in units such as mg As/kg of rib or μg As/g of rib or simply ppm; that is, part of As per million parts of rib.

The quantification analytical procedure was conducted on the solubilized rib sample in an aliquot in a volumetric flask of a defined total volume and conditioned to a concentration of 1 M HCl and of potassium iodide (KI) at 1% mass/volume. The total mixture was homogenized and absorbed simultaneously into the Agilent Technologies VGA 77 continuous flow system through line 1. This was conducted in parallel with the absorption of a 5 M hydrochloric acid (HCl) solution through line 2 and of a reducing reagent, sodium borohydride (NaBH4) of concentration 0.6% mass/volume in sodium hydroxide 0.5% mass/volume. The reagent mixture transformed the As element in the solution into the gaseous arsenamine or As hydride (AsH3), a gas phase that is transported by the nitrogen gas in the system, with a continuous flow, to the atomization cell of the Agilent Technologies 240FS AA atomic absorption instrument, where the As concentration was quantified.

The different instrumental quantification operations were achieved based on the instrumental conditions shown in Table 2.

Table 2. Equipment Specifications.

Statistical Analysis

We first calculated z-values to exclude outliers or extreme cases (z > 3), keeping 99.7% of the most representative cases. Then, we conducted a descriptive analysis of the As concentrations in the rib samples and a statistical contrast of means in the sex variable using Student's t-test. Analysis of the presence of arsenic in ribs according to age ranges using the Shapiro-Wilk test showed that they were not normally distributed. Consequently, the Kruskal-Wallis test was performed, which determined no significant differences between the groups.

To establish a comparative reference standard, we gathered data on current As concentrations in the water sources found in the three main valleys of the northern zone of Chile (Table 3) and the maximum values of As in the human bone matrix, according to global health organizations, such as WHO.

Table 3. Summary of Arsenic Concentration Levels in the Main Water Sources of Northern and Central Chile.

Results

The overall sample (N = 16; Table 4) showed a median of 2.2 μg/g for As in bones (mean = 3.4, SD = 3.1, minimum = 0.2, maximum = 9.3). However, in 12 individuals (75%), the presence of As in the bone matrix was above the level recommended by WHO (1 μg/g); this increased these individuals’ median to 3.6 μg/g (mean = 4.3. SD = 3.0, minimum = 1.4, maximum = 9.3). Both males and females were affected, and no cases of extreme outliers (z > 3) or significant differences between sexes were observed (t = 2.78 [2 tails], p = 0.19). In the sample, individuals in all the age categories showed As median values higher than the recommended 1 μg/g: adolescents = 2.6 μg/g, young adults = 8.8 μg/g, middle adults = 1.4 μg/g, and older adults = 5.2 μg/g. Three individuals—one young female, one older female, and one young male—had levels about nine times higher than the WHO recommended values (Table 4).

Table 4. Arsenic Values Obtained for the Analyzed Mummies.

Discussion

Previous archaeological analyses, such as studies on headdresses (Horta Reference Horta2000, Reference Horta2011a), support the presence of a foreign fishing population in Camarones Cove at the end of the Late Intermediate period (ca. AD 1000–1450). Similarly, Muñoz (Reference Muñoz1989:95) states, “The late settlement of the Desembocadura del Río Camarones is framed within this same population structure; that is, groups with a wide domain of the sea and that work on the land, interacting with populations linked to a pre-Inca and later Inca Altiplanic tradition” (translation by the authors). In addition, coastal technological elements—such as rafts, capacacho baskets, harpoon holders, copper hooks, and harpoons with copper barbs for fishing—and fishing for deep-sea species would have caused an increase in surplus (e.g., dried fish), facilitating exchange with inland populations (Horta Reference Horta2000, Reference Horta2011b; Llagostera Reference Llagostera1990; Muñoz Reference Muñoz1989; Núñez 1986). Therefore, a nonlocal population likely inhabited the Camarones coast, was assigned to carry out productive tasks, and suffered the consequences of a quietly hidden toxic environment. This hostile environment was paradoxically near a river mouth that stood out due to the beauty of its landscape, with a large wetland and abundance of birds and coastal fauna.

Populations that are suddenly exposed to highly arsenical waters are at high risk of arseniasis. Two epidemiological examples validate this point. Millions of people in many districts of Bangladesh have become poisoned since the 1990s due to the use of deep tube wells containing levels of arsenic of 100 μg/L (Ahmad et al. Reference Ahmad, Salim Sayed, Barua, Khan, Faruquee, Jalil, Abdul Hadi and Talukder2001; Alam et al. Reference Alam, Allinson, Stagnitti, Tanaka and Westbrooke2002). In the second case, a massive intoxication occurred in Antofagasta City in Chile in the 1960s when mining activities led to a shortage of freshwater. The Toconce River, which contains 800 μg/L of arsenic, was connected to the main street water system. Soon after, people began to experience multiple health problems linked to arsenic in the water (Arriaza and Galaz-Mandakovic Reference Arriaza and Galaz-Mandakovic2020; Hopenhayn et al. Reference Hopenhayn, Ferreccio, Browning, Huang, Peralta, Gibb and Hertz-Picciotto2003; Hopenhayn-Rich et al. Reference Hopenhayn-Rich, Browning, Hertz-Picciotto, Ferreccio, Peralta and Gibb2000).

Similarly, foreign populations without previous adaptation to high levels of As and who settle in an arsenical area to exploit its natural resources face a potential health risk by exposing themselves to a new, naturally contaminated environment. In our study, 75% of the individuals buried in CAM-9 presented As values in their ribs that were higher than the norm. Arsenic bone values were 3.6 times higher (median) than the recommended limit, with some reaching up to nine times higher on average (Table 4). In addition, individuals in every age category were significantly affected, ranging between an average As bone value of 2.5 and 7.3 times above the recommended values. Archaeometric analyses of different types of matrices (e.g., hair, bone, and soft tissue) demonstrate that ancient populations of CAM-9 were significantly exposed to As, showing various manifestations of arseniasis at the somatic level independent of sex and age (Arriaza et al. Reference Arriaza, Dulasiri Amarasiriwardena, Vivien Standen, Bartkus and Bandak2010; Figueroa Reference Figueroa2001; Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988). Unfortunately, there were no satisfactory bioanthropological collections available from Camarones to test the complete cultural sequence of human adaptation and exposure to As.

In addition to high levels of arsenic in bones, macroscopic skin lesions observed in CAM-9 in previous studies (Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988) are relevant because they provide a visible sign of a somatic alteration with arsenical etiology. Similarly, the bodies in CAM-9 presented very high concentrations of As in their organs, with average values between three and 342 times above the norm, depending on the analyzed tissue (Figueroa et al. Reference Figueroa, Razmilic, Allison and González1988). This evidence, in conjunction with the high prevalence of spina bifida occulta in CAM-9 individuals (Silva et al. Reference Silva, Arriaza and Standen2010), reinforces the hypothesis that the population of CAM-9 was exposed for the first time to an arsenical environment and suffered from severe arseniasis after settling in the Camarones Valley and drinking the highly contaminated waters. The most plausible explanation is that this population had no natural resistance to As and may represent a new population (mitimaes) that originated from less contaminated environments. In other words, they did not have the genetic makeup to tolerate or eliminate the As, leading to many health problems.

Increasingly, research demonstrates that after multiple generations have lived in arsenic-rich environments, adaptation to this poisonous element occurs. For instance, modern populations from northern Chile (Camarones) and Argentina (San Antonio de los Cobres, SAC) that have been exposed to arsenical environments demonstrate genetic variants (AS3MT) that help them methylate and excrete As: they have adapted to this invisible environmental toxin and can ingest it without experiencing negative consequences to their health (Apata et al. Reference Apata, Arriaza, Llop and Moraga2017; Eichstaedt et al. Reference Eichstaedt, Antao, Cardona, Pagani, Kivisilda and Mormina2015; Schlebusch et al. Reference Schlebusch, Lewis, Vahter, Engström, Tito, Obregón-Tito and Huerta2013). According to Yáñez and colleagues (Reference Yáñez, Mansilla, Paola Santander, Fierro, Cornejo, Barnes and Amarasiriwardena2015:7), “It appears that exposure to higher concentrations of arsenic (V) would eventually enhance the methylation capability by the liver leading into a more efficient elimination of ingested arsenic body burden through urine.” In addition, several studies conducted in modern populations from Camarones and SAC showed that the AS3MT enzyme plays an important role in the elimination of the ingested toxic As (Apata et al. Reference Apata, Arriaza, Llop and Moraga2017; Eichstaedt et al. Reference Eichstaedt, Antao, Cardona, Pagani, Kivisilda and Mormina2015; Schlebusch et al. Reference Schlebusch, Lewis, Vahter, Engström, Tito, Obregón-Tito and Huerta2013; Vicuña et al. Reference Vicuña, Fernandez, Vial, Valdebenito, Chaparro, Espinoza, Annemarie Ziegler and Eyheramendy2019). Approximately 68% of the modern people of Camarones and SAC carry such a protected variant, specifically the CTA haplotype (Apata et al. Reference Apata, Arriaza, Llop and Moraga2017; Schlebusch et al. Reference Schlebusch, Lewis, Vahter, Engström, Tito, Obregón-Tito and Huerta2013).

If, indeed, the samples recovered from CAM-9 represent newcomers to the region who suffered from arseniasis, then future ancient DNA studies should demonstrate that CAM-9 individuals carried a low percentage of the AS3MT protective variant. In addition, the origin of the CAM-9 population remains to be determined in future studies: Were they members of Altiplanic groups, or did they come from coastal areas (e.g., from Arica or southern Peru) and were then transferred to Camarones? Similarly, how the CAM-9 population was integrated into nearby sites in the same valley, such as CAM-12 (north slope of the Camarones River mouth) and Saguara (inland of Camarones valley), should be investigated.

The arsenicism (skin lesions, high systemic intoxication, etc.) observed in the CAM-9 individuals most likely affected their daily lives. The CREHA experienced by this displaced population probably carried aspects of emotional burden and stigma for those chronically affected. Highly visible skin lesions, together with other systemic arsenic-related pathologies, may have reduced the desirability of affected individuals, minimizing their reproductive and labor success. Ethnographic data show that women from Bangladesh affected with skin lesions due to hydroarsenic poisoning are socially very vulnerable and are often stigmatized or abandoned by their husbands. In addition, some affected young women are unable to marry (Alam et al. Reference Alam, Allinson, Stagnitti, Tanaka and Westbrooke2002; Hassan et al. Reference Hassan, Atkins and Dunn2005). One could speculate that similar problems or some social stigma occurred among heavily affected individuals from CAM-9.

In addition, the various types of symptoms and pathology produced by CREHA must have affected productivity and their tribute to the Inca in communities associated with the CAM-9 cemetery. Carmona (Reference Carmona2004) shows that in CAM-9 most of the shirts were repaired and reused, illustrating a difficult life. These data suggest a biologically and socially affected population.

Conclusions

CAM-9 represents the final period of the precontact sequence of fishermen from the extreme north of Chile. Based on the bioarchaeological data presented, we posit that it housed a population of mitimaes newly settled in an arsenic-laden environment. In addition, their grave goods suggest that the Inca moved the CAM-9 population to this coastal environment to exploit marine resources. The high concentrations of As found in various tissues of CAM-9 mummies confirm that it represents an allochthonous population that was not previously exposed to high As contents. Therefore, arsenic-laden water must have significantly affected both the health of the population and their assigned functions and productive capacity. However, the biogeographic origin of CAM-9, whether coastal or highland, is unresolved.

We conclude that environments in the past that seemed paradisiacal to settle in because of their abundance of exploitable natural resources instead presented hidden and lethal risks. These environments subjected their inhabitants to a process of adaptation that had biological, cultural, and economic costs. Consequently, when discussing cultural trajectories of ancient populations, it is of vital importance to incorporate the potential inorganic hazards of a given environment. This study highlights the importance of natural water pollution in the diaspora of the Andean populations; it generates new debates and proposals on the role of natural contamination and its consequences in the appropriation of space for human settlement, in both favorable and unfavorable conditions, while exploiting multiple ecological niches in different cultural periods. This study is relevant to all regions of the world that present ecotoxic loads, such as hydroarsenicism, as well as in the human diaspora at different moments of prehistory and universal history.

Acknowledgments

We are grateful for the funding of Fondecyt 1170120 and 1210036. We acknowledge the support of the Museo Arqueológico San Miguel de Azapa, the Chemistry Department, and the Instituto de Alta Investigación, all from the Universidad de Tarapacá, Arica, for the execution of this project. We thank Camila Contreras, Natalia Aravena, Anita Flores, and Susana Monsalve for their laboratory collaboration and Arnoldo Vizcarra for assistance with the preparation of figures. Our gratitude to the anonymous reviewers for their insightful comments and suggestions.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author on request.

Competing Interests

The authors declare none.

References

References Cited

Ahmad, Sk. Akhtar, Salim Sayed, M. H., Barua, Shampa, Khan, Manzurul, Faruquee, Mohammad, Jalil, Abdul, Abdul Hadi, S., and Talukder, Humayun 2001 Arsenic in Drinking Water and Pregnancy Outcomes. Environmental Health Perspectives 109:629631.10.1289/ehp.01109629CrossRefGoogle ScholarPubMed
Alam, Maqadus, Allinson, Graeme, Stagnitti, Frank, Tanaka, Atsushi, and Westbrooke, Martin 2002 Arsenic Contamination in Bangladesh Groundwater: A Major Environmental and Social Disaster. International Journal of Environmental Health Research 12:236253.CrossRefGoogle Scholar
Álvarez, Luis 2014 Etnopercepción andina: Valles dulces y valles salados en la vertiente occidental de los Andes. Diálogo Andino 44:514.10.4067/S0719-26812014000200002CrossRefGoogle Scholar
Apata, Mario, Arriaza, Bernardo, Llop, Elena, and Moraga, Mauricio 2017 Human Adaptation to Arsenic in Andean Populations of the Atacama Desert. American Journal of Physical Anthropology 163:192199.10.1002/ajpa.23193CrossRefGoogle ScholarPubMed
Arenas H., Alejandro 2016 Estudio diagnóstico de disponibilidad hídrica cuenca del Río Camarones. Chile, Dirección General de Aguas, División de Estudios y planificación. https://bibliotecadigital.ciren.cl/handle/20.500.13082/32717, accessed May 31, 2021.Google Scholar
Arriaza, Bernardo 2021 Bioarchaeology of the Invisible: Unraveling the History of Endemic Natural Contaminants that May Have Affected Ancient Chilean Populations. Final Report FONDECYT Project N° 1170120. Submitted to FONDECYT. Copies available from Bioarchaeology Laboratory, Instituto de Alta Investigación, Universidad de Tarapacá, Arica, Chile.Google Scholar
Arriaza, Bernardo, Dulasiri Amarasiriwardena, Lorena Cornejo, Vivien Standen, Sam Byrne, Bartkus, Luke, and Bandak, Basel 2010 Exploring Chronic Arsenic Poisoning in Pre-Columbian Chilean Mummies. Journal of Archaeological Science 37:12741278.10.1016/j.jas.2009.12.030CrossRefGoogle Scholar
Arriaza, Bernardo, Amarasiriwardena, Dulasiri, Standen, Vivien, Yáñez, Jorge, Van Hoesen, John, and Figueroa, Leonardo 2018 Living in Poisoning Environments: Invisible Risks and Human Adaptation. Evolutionary Anthropology 27:188196.10.1002/evan.21720CrossRefGoogle ScholarPubMed
Arriaza, Bernardo, and Galaz-Mandakovic, Damir 2020 Expansión minera, déficit hídrico y crisis sanitaria: La potabilización del río Toconce y el impacto del arsenicismo en la población de la provincia de Antofagasta (1915-1971). Historia 396:71112.Google Scholar
Arriaza, Bernardo, Huaman, Luis, Villanueva, Fiorella, Tornero, Roxana, and Aravena, Natalia 2018 Estudio del cálculo dental en poblaciones arqueológicas del extremo norte de Chile. Estudios Atacameños 60:297312.Google Scholar
Arriaza, Bernardo, Standen, Vivien, Heukelbach, Jorg, Cassman, Vicki, and Olivares, Felix 2014 Head Combs for Delousing in Ancient Arican Populations: Scratching for the Evidence. Chungara 46:693706.Google Scholar
Barrientos, Gustavo, Sarmiento, Patricia, and Galligani, Paula 2016 Evaluación de la diagénesis ósea mediante el uso de Microscopía Electrónica de Barrido (MEB): Aproximaciones analíticas aplicables a muestras arqueológicas. Revista Argentina de Antropología Biológica 18(2):113.CrossRefGoogle Scholar
Bigham, Abigail, and Lee, Frank 2014 Human High-Altitude Adaptation: Forward Genetics Meets the HIF Pathway. Genes and Development 28:21892204.10.1101/gad.250167.114CrossRefGoogle ScholarPubMed
Brito, Yaritza 2020 Análisis bioarqueológico de los infantes provenientes de los sitios Camarones 8 y Camarones 9 y su relación con la contaminación medioambiental. Undergraduate thesis, Facultad de Ciencias Sociales y Jurídicas, Departamento de Antropología, Universidad de Tarapacá, Arica, Chile.Google Scholar
Brooks, Sheilagh, and Suchey, Judy Myers 1990 Skeletal Age Determination Based on the Os Pubis: A Comparison of the Ascádi-Nemeskéri and Suchey–Brooks Methods. Human Evolution 5:227238.CrossRefGoogle Scholar
Buikstra, Jane, and Ubelaker, Douglas (editors) 1994 Standards for Data Collection from Human Skeletal Remains. Research Series No. 44. Arkansas Archeological Survey, Fayetteville.Google Scholar
Bundschuh, Jochen, Nicolli, Hugo, Blanco, María del C., Blarasin, Mónica, Farías, Silvia, Cumbal, Luis, Cornejo, Lorena, et al. 2008 Distribución de arsénico en la Región Sudamericana. In Iberoarsen: Distribución del arsénico en las Regiones Ibérica e Iberoamericana, edited by Bundschuh, Jochen, Carrera, Alejo Pérez, and Litter, Marta, pp. 137186. Cyted, Argentina.Google Scholar
Byrne, Sam, Amarasiriwardena, Dulasiri, Bandak, Basel, Bartkus, Luke, Kane, Jennifer, Jones, Joseph, Yáñez, Jorge, Arriaza, Bernardo, and Cornejo, Lorena 2010 Were Chinchorros Exposed to Arsenic? Arsenic Determination in Chinchorro Mummies’ Hair by Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS). Microchemical Journal 94:2835.CrossRefGoogle Scholar
Carmona, Gabriela 2004 Los textiles en el contexto multiétnico del Período Tardío en Arica. Chungara 36:249260.Google Scholar
Cassman, Vicki 2000 Prehistoric Ethnicity and Status Based on Textile Evidence from Arica, Chile. Chungara 32:253257.Google Scholar
de Esparza, Castro, Luisa, María 2004 Arsénico en el agua de bebida de América Latina y su efecto en la salud pública. Hojas de Divulgación Técnica 95:112.Google Scholar
Catalán, Danisa 2008 Reacciones locales frente al Tawantinsuyu: Una aproximación desde los contextos funerarios (el Período Tardío en los Valles Occidentales). Master's thesis, Departamento de Antropología Universidad de Tarapacá-Universidad Católica del Norte, Arica, Chile.Google Scholar
Cornejo, Lorena 2004 Reducción de la concentración de arsénico en agua de consumo humano en zonas rurales. Paper presented at the Encuentro sobre uso y resultados de la aplicación de tecnologías económicas para la purificación de aguas en América Latina, Proyecto OEA/AE 141. Centro Atómico Constituyentes, Comisión Nacional de Energía Atómica, Buenos Aires.Google Scholar
Cornejo, Lorena, Lienqueo, Hugo, Arriaza, Bernardo, Acarapi, Jorge, and Arenas, María 2008. Comparación de los niveles de arsénico total en la especie silvestre Cyperaceae scirpus sp y suelos superficiales de tres valles del norte de Chile. Paper presented at the Congreso Iberoamericano de Química, XXIV Congreso Peruano de Química, Cusco, Peru.Google Scholar
DGA (Dirección General de Aguas/General Water Directorate, Gobierno de Chile) 2019 Información oficial hidrometeorológica y de calidad de aguas en línea. https://snia.mop.gob.cl/BNAConsultas/reportes, accessed October 15, 2019.Google Scholar
Echeverría, Javier, Niemeyer, Hermann M., Muñoz, Luis, and Uribe, Mauricio 2018 Arsenic in the Hair of Mummies from Agro-Ceramic Times of Northern Chile (500 BCE–1200 CE). Journal of Archaeological Science: Reports 21:175182.Google Scholar
Eichstaedt, Cristina, Antao, Tiago, Cardona, Alexia, Pagani, Luca, Kivisilda, Toomas, and Mormina, Maru 2015 Positive Selection of AS3MT to Arsenic Water in Andean Populations. Mutation Research 780:97102.10.1016/j.mrfmmm.2015.07.007CrossRefGoogle ScholarPubMed
Ferreccio, Catterina, González, Claudia, Milosavjlevic, Vivian, Marshall, Guillermo, Sancha, Ana Maria, and Smith, Allan 2000 Lung Cancer and Arsenic Concentrations in Drinking Water in Chile. Epidemiology 11:673679.CrossRefGoogle ScholarPubMed
Figueroa, Leonardo 2001 Arica inserta en una región arsenical: El arsénico en ambiente que la afecta: 45 siglos de arsenicismo crónico. Ediciones Universidad de Tarapacá. Arica, Chile.Google Scholar
Figueroa, Leonardo, Razmilic, Blago, Allison, Marvin, and González, Mariluz 1988 Evidencia de arsenicismo crónico en momias del valle Camarones. Chungara 21:3342.Google Scholar
González-Holguín, Diego 1952 [1608] Vocabulario de la lengua general de todo el Perú llamada lengua qqichua o del inca. Universidad Nacional Mayor de San Marcos, Lima.Google Scholar
Hassan, Manzurul, Atkins, Peter, and Dunn, Christine 2005 Social Implications of Arsenic Poisoning in Bangladesh. Social Science and Medicine 61:22012211.CrossRefGoogle ScholarPubMed
Hidalgo, Jorge 2004 Pescadores del litoral árido de valles y quebradas del Norte de Chile y su relación con agricultores, siglos XVI y XVII. In Historia Andina en Chile, edited by Hidalgo, Jorge, pp. 431469. Editorial Universitaria, Santiago.Google Scholar
Hidalgo, Jorge, and Focacci, Guillermo 1986 Multietnicidad en Arica, Siglo XVI, evidencias etnohistóricas y arqueológicas. Chungara 16–17:137147.Google Scholar
Hopenhayn, Claudia, Ferreccio, Catterina, Browning, Steven R., Huang, Bin, Peralta, Cecilia, Gibb, Herman, and Hertz-Picciotto, Irva 2003 Arsenic Exposure from Drinking Water and Birth Weight. Epidemiology 14:593602.CrossRefGoogle ScholarPubMed
Hopenhayn-Rich, Claudia, Browning, Steven R., Hertz-Picciotto, Irva, Ferreccio, Catterina, Peralta, Cecilia, and Gibb, Herman 2000 Chronic Arsenic Exposure and Risk of Infant Mortality in Two Areas of Chile. Environmental Health Perspectives 108:667673.CrossRefGoogle ScholarPubMed
Horta, Helena 2000 Diademas de plumas en entierros de la costa del norte de Chile: ¿Evidencias de la vestimenta de una posible parcialidad pescadora? Chungara 32:235243.Google Scholar
Horta, Helena 2011a El gorro troncocónico o chucu y la presencia de población altiplánica en el norte de Chile durante el periodo tardío (ca. 1.470–1.536 D.C.). Chungara 43(Número especial 1):551580.Google Scholar
Horta, Helena 2011b Nuevos indicadores arqueológicos de la presencia altiplánica en Valles Occidentales durante el Período Tardío. In Actas de la XXIII Reunión Anual de Etnología, pp. 1740. Museo Nacional de Etnografía y Folklore (MUSEF), La Paz.Google Scholar
Horta, Helena 2015 El señorío Arica y los Reinos Altiplánicos (1.000–1.540 d.C.): Complementariedad ecológica y multietnicidad durante los siglos pre-conquista en el Norte de Chile. Quillqa Ediciones IAA, Santiago de Chile.Google Scholar
Kakoulli, Ioanna, Prikhodko, Sergey, Fischer, Christian, Cilluffo, Marianne, Uribe, Mauricio, Bechtel, Hans, Fakra, Sirine, and Marcus, Matthew 2014 Distribution and Chemical Speciation of Arsenic in Ancient Human Hair Using Synchrotron Radiation. Analytical Chemistry 86:521526.CrossRefGoogle ScholarPubMed
Litter, Marta, and Bundschuh, Jochen (editors) 2010 Iberoarsen: Situación del arsénico en la Región Ibérica e Iberoamericana: Posibles acciones articuladas e integradas para el abatimiento del arsénico en zonas aisladas. Editorial Programa Iberoamericano de Ciencia y Tecnología para el Desarrollo, Buenos Aires.Google Scholar
Llagostera, Agustín 1990 La navegación prehispánica en el Norte de Chile: Bioindicadores e inferencias teóricas. Chungara 24–25:3751.Google Scholar
Lovejoy, C. Owen, Meindl, Richard S., Pryzbeck, Thomas R., and Mensforth, Robert P. 1985 Chronological Metamorphosis of the Auricular Surface of the Ilium: A New Method for the Determination of Adult Skeletal Age at Death. American Journal of Physical Anthropology 68:1528.CrossRefGoogle ScholarPubMed
McClintock, Tyler R., Chen, Yu, Bundschuh, Jochen, Oliver, John T., Navoni, Julio, Olmos, Valentina, Lepori, Edda Villaamil, Ahsan, Habibul, and Parvez, Faruque 2012 Arsenic Exposure in Latin America: Biomarkers, Risk Assessments and Related Health Effects. Science of the Total Environment 429:7691.CrossRefGoogle ScholarPubMed
Muñoz, Iván 1989 Perfil de la organización económica social en la desembocadura del río Camarones. Períodos Intermedio Tardío e Inca. Chungara 22:85111.Google Scholar
Murra, John 1972 El Control vertical de un máximo de pisos ecológicos en la economía de las sociedades andinas. Universidad Hermilio Valdizán, Huánuco, Peru.Google Scholar
NCh (Norma chilena oficial 409 [NCh409/1.Of2005]) 2005 Agua potable parte I requisitos. Electronic document, http://ciperchile.cl/pdfs/11-2013/norovirus/NCh409.pdf, accessed May 31, 2021.Google Scholar
Niemeyer, Hans 1980 Hoyas hidrográficas de Chile: Primera Región. Dirección General de Aguas. Centro de Información, Recursos Hídricos, Santiago.Google Scholar
Noack, Karoline 2018 Los mitimaes temían a los naturales y los naturales a los mitimaes: Políticas de reasentamiento y la construcción de la diferencia en el Estado inca. Surandino Monográfico 4:2338.Google Scholar
Núñez, Lautaro 1986 Balsas prehistóricas del litoral chileno: Grupos, funciones y secuencias. Boletín del Museo Chileno de Arte Precolombino 1:1135.Google Scholar
Rostworowski de Diez Canseco, María 1986 La región del Colesuyu. Chungara 16–17:127135.Google Scholar
Ruiz, Esther, and Armienta, Maria 2012. Acumulación de arsénico y metales pesados en maíz en suelos cercanos a jales o residuos mineros. Revista Internacional de Contaminación Ambiental 28:103117.Google Scholar
Santoro, Calogero, and Muñoz, Iván 1981 Patrón habitacional incaico en el área de Pampa Alto Ramírez (Arica Chile). Chungara 7:144171.Google Scholar
Santoro, Calogero, Romero, Álvaro, Standen, Vivien, and Valenzuela, Daniela 2009 Interacción social en los Períodos Intermedio Tardío y Tardío, Valle de Lluta, Norte de Chile. In La arqueología y la etnohistoria: Un encuentro Andino, edited by Topic, John, pp. 81137. IEP-IAR, Lima.Google Scholar
Schiappacasse, Virgilio, and Niemeyer, Hans 1989 Avances y sugerencias para el conocimiento de la prehistoria tardía en la desembocadura del valle de Camarones (región de Tarapacá). Chungara 22:6384.Google Scholar
Schiappacasse, Virgilio, and Niemeyer, Hans 2002 Ceremonial inca provincial: El asentamiento de Saguara (Cuenca de Camarones). Chungara 34:5384.Google Scholar
Schlebusch, Carina M., Lewis, Cecil M. Jr., Vahter, Marie, Engström, Karin, Tito, Raúl Y., Obregón-Tito, Alexandra J., Huerta, Doris, et al. 2013 Possible Positive Selection for an Arsenic-Protective Haplotype in Humans. Environmental Health Perspectives 121:5358.10.1289/ehp.1205504CrossRefGoogle ScholarPubMed
Schull, William J., Blago Razmilic, Leonardo Figueroa, and González, Mariluz 1990 Trace Metals. In The Aymará: Strategies in Human Adaptation to a Rigorous Environment, edited by Schull, William and Rothhammer, Francisco, pp. 3344. Kluwer Academic, Boston.CrossRefGoogle Scholar
Silva, Verónica, Arriaza, Bernardo, and Standen, Vivien 2010 Evaluación de la frecuencia de espina bífida oculta y su posible relación con el arsénico ambiental en una muestra prehispánica de la Quebrada de Camarones, norte de Chile. Revista Médica de Chile 138:461469.Google Scholar
Standen, Vivien, Arriaza, Bernardo, and Santoro, Calogero 1997 External Auditory Exostosis in Prehistoric Chilean Populations: A Test of the Cold Water Hypothesis. American Journal of Physical Anthropology 103:119129.10.1002/(SICI)1096-8644(199705)103:1<119::AID-AJPA8>3.0.CO;2-R3.0.CO;2-R>CrossRefGoogle ScholarPubMed
Swift, Jaime, Cupper, Matthew L., Greig, Alan, Westaway, Michael, Carter, Chris, Santoro, Calogero, Wood, Rachel, Jacobsen, Geraldine E., and Bertuch, Fiona 2015 Skeletal Arsenic of the Pre-Columbian Population of Caleta Vitor, Northern Chile. Journal of Archaeological Science 58:3145.10.1016/j.jas.2015.03.024CrossRefGoogle Scholar
Tondel, Martin, Rahman, Mahfuzar, Magnuson, Anders, Chowdhury, Ireen, Faruquee, Mohammad, and Ahmad, Sk. Akhtar 1999 The Relationship of Arsenic Levels in Drinking Water and the Prevalence Rate of Skin Lesions in Bangladesh. Environmental Health Perspectives 107:727729.CrossRefGoogle ScholarPubMed
Ulloa, Liliana, Standen, Vivien, and Gavilán, Vivian 2000 Estudio de una prenda textil asociada al Inca en la costa norte de Chile (Camarones 9): Las “mantas” que envuelven los cuerpos. Chungara 32:259261.Google Scholar
Vicuña, Lucas, Fernandez, Mario I., Vial, Cecilia, Valdebenito, Patricio, Chaparro, Eduardo, Espinoza, Karena, Annemarie Ziegler, Alberto Bustamante, and Eyheramendy, Susana 2019 Adaptation to Extreme Environments in an Admixed Human Population from the Atacama Desert. Genome Biology and Evolution 11:24682479.CrossRefGoogle Scholar
WHO, (World Health Organization) 2003 Arsenic in Drinking-Water; Background Document for Development of WHO Guidelines for Drinking-Water Quality. WHO/SDE/WSH/03.04/75/rev1. https://apps.who.int/iris/rest/bitstreams/104501/retrieve, accessed January 22, 2018.Google Scholar
WHO, (World Health Organization) 2006 Guidelines for Drinking-Water Quality, Vol 1. 3rd ed. World Health Organization, Geneva.Google Scholar
WHO, (World Health Organization) 2008 Guidelines for Drinking-Water Quality: Third Edition Incorporating the First and Second Addenda, Volume 1: Recommendations. https://apps.who.int/iris/handle/10665/204411, accessed September 27, 2022.Google Scholar
Yáñez, Jorge, Fierro, Vladimir, Mansilla, Héctor, Figueroa, Leonardo, Cornejo, Lorena, and Barnes, Ramón M. 2005 Arsenic Speciation in Human Hair: A New Perspective for Epidemiological Assessment in Chronic Arsenicism. Journal of Environmental Monitoring 7:13351341.CrossRefGoogle Scholar
Yáñez, Jorge, Mansilla, Héctor D., Paola Santander, I., Fierro, Vladimir, Cornejo, Lorena, Barnes, Ramón M., and Amarasiriwardena, Dulasiri 2015 Urinary Arsenic Speciation Profile in Ethnic Group of the Atacama Desert (Chile) Exposed to Variable Arsenic Levels in Drinking Water. Journal of Environmental Science and Health, Part A, 50:18.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. General diagram of overexposure to arsenic.

Figure 1

Figure 2. Map illustrating the location of the archaeological sites mentioned.

Figure 2

Figure 3. Surrounding area of CAM-9 site and terrace, showing the fertility of the river delta (photograph by Carlos Chow). (Color online)

Figure 3

Table 1. Radiocarbon Dates of the CAM-9 Site.

Figure 4

Figure 4. Complete undisturbed tomb, with its grave goods (harpoons, shafts, bags, and a vessel) and cephalic headdress possibly made of Otaria sp. filaments (CAM-9 Tomb 11) (photograph by Vivien Standen). (Color online)

Figure 5

Figure 5. Detail of headdress made of possible Otaria sp. filaments (CAM-9 Tomb 11) (photograph by Vivien Standen). (Color online)

Figure 6

Table 2. Equipment Specifications.

Figure 7

Table 3. Summary of Arsenic Concentration Levels in the Main Water Sources of Northern and Central Chile.

Figure 8

Table 4. Arsenic Values Obtained for the Analyzed Mummies.