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International Journal of Osteoarchaeology

Int. J. Osteoarchaeol. 23: 287–302 (2013)


Published online 24 February 2011 in Wiley Online Library
(wileyonlinelibrary.com) DOI: 10.1002/oa.1247

Tooth Wear Related to Marine Foraging,


Agro‐Pastoralism and the Formative
Transition on the Northern Chilean Coast
J. T. WATSON,a* B. ARRIAZA,b,c V. STANDENc AND I. MUÑOZ OVALLEc
a
Arizona State Museum and School of Anthropology, University of Arizona, PO Box 210026, Tucson,
AZ 85721, USA
b
Instituto de Alta Investigación and Centro de Investigaciones del Hombre en el Desierto, Universidad
de Tarapacá, Arica, Chile
c
Departamento de Antropología, Universidad de Tarapacá, Arica, Chile

ABSTRACT Occlusal surface wear scores were examined in a sample of 200 Formative period (1500 BC–AD 500)
skeletons from the lower Azapa Valley in northwest Chile. Wear rate and plane (angle) were additionally
evaluated using a subsample of paired first and second mandibular molars. The Formative period represents
the transition from marine foraging to agro‐pastoral dependence in the region, and differences in oral
pathology indicate that diet varied by site location (coast vs valley interior) but not by archaeological phase
(early vs late). We predicted that occlusal wear would demonstrate similar patterns, resulting from
differences in food consistency, and therefore hypothesised that in coastal groups consuming greater
quantities of foraged foods, occlusal surfaces should wear faster and exhibit flat molar wear, whereas among
valley interior groups consuming greater quantities of agro‐pastoral products, these should wear slower but
exhibit more angled molar wear. Heavier posterior tooth wear was identified among coastal residents, but
rate and angle of molar occlusal attrition did not differ significantly by location. Heavier overall wear and a
steeper molar wear plane were identified during the early phase indicating that food consistency varied
somewhat over the course of the Formative period. Overall, the results indicate that, although limited
differences in tooth wear exist by site location, wear varied more over time likely reflecting a gradual transition
from foraging to agro‐pastoral dependence in the lower Azapa Valley. Although oral health indicators point to
differences in dietary investment by location, maintenance of a mixed subsistence economy likely sustained
a comparative consistency of foodstuffs. Copyright © 2011 John Wiley & Sons, Ltd.

Key words: Chile; Formative period; marine foraging; occlusal wear plane; tooth wear

Changes in diet and subsistence patterns associated reconstruction of dietary behaviours of past populations,
with the ‘Neolithic Revolution’ (Childe, 1925) had refining our understanding of the health consequences of
profound effects on the oral health of past populations the agricultural transition (Molnar, 1971; Smith, 1984;
on a global scale (Cohen & Armelagos, 1984; Steckel & Sciulli, 1997; Pechenkina et al., 2002; Chattah & Smith,
Rose, 2002; Cohen & Crane‐Kramer, 2007). The 2006; Watson, 2008a, 2008b; Deter, 2009; Fujita &
adoption of agriculture often caused a reduction in Ogura, 2009; Liu et al., 2010).
dietary breadth and created a softer, more processed diet Wear of the occlusal tooth surface is a multifactorial
that resulted in increased oral disease, uneven tooth wear process that results from three main interacting
and malocclusion (Molnar, 1971; Smith, 1984; Larsen, mechanisms: attrition, abrasion and erosion (Kaidonis
1997; Hillson, 2002). In addition, the aetiologies of oral et al., 1988; Miles, 2001; Hillson, 2002). Attrition is
diseases and differential tooth wear frequently interact caused by wear of the tooth surface through friction
and co‐contribute to the advancement of each other resulting from tooth‐on‐tooth contact (Larsen, 1981,
(Hillson, 2002). However, they can also be quantified 2002; Milner & Larsen, 1991; Lukacs, 1992; Hillson,
individually in skeletal samples and used to aid in the 2002). Abrasion is the loss of surface detail from friction
with exogenous material (Kaidonis et al., 1988; Hillson,
2002). Erosion is the reduction of dental surfaces due to
* Correspondence to: Arizona State Museum, University of Arizona, PO
Box 210026, Tucson, AZ 85721-0026, USA. non‐bacterial exogenous or endogenous chemical
e-mail: watsonjt@email.arizona.edu substances (Kieser et al., 2001). Each of these processes

Copyright © 2011 John Wiley & Sons, Ltd. Received 16 July 2010
Revised 31 December 2010
Accepted 19 January 2011
288 J. T. Watson et al.

is continuous, unidirectional and age progressive Occlusal wear angle in the molar region is shaped by
(Miles, 2001; Hillson, 2002). A number of studies have differential wear of the buccal and lingual cusps
successfully correlated differences in the rates and (Reinhardt, 1983; Hillson, 2002). With progressive
patterns of these wear processes to differences in overall wear, steeper occlusal planes develop from lingual to
subsistence practices among pre‐industrial populations, buccal in mandibular molars and buccal to lingual in
where occlusal wear is generally severe (Molnar, 1971; maxillary molars, with each molar generating steeper
Smith, 1984; Larsen, 1997; Kaifu, 1999; Kieser et al., angles or wear planes in order of molar eruption
2001; Deter, 2009; Fujita & Ogura, 2009; Liu et al., sequence, eventually resulting in a reversed curve of
2010). Food consistency and the presence of foreign Monson (Osborn, 1984). This pattern becomes more
abrasives have been shown to significantly influence the apparent in agricultural groups where the consumption
rate of occlusal tooth wear (Hillson, 2002). of a narrower dietary breadth and heavily processing
The wear plane (or angle) of the occlusal surface has foodstuffs reduces chewing resistance and lateral
similarly been shown to differ measurably between movements, increasing the amount of contact between
skeletal samples of diverse subsistence economies cusps and creating steeper occlusal plane angles at
(Molnar, 1971; Smith, 1984; Pechenkina et al., 2002; faster rates (Smith, 1984). Smith (1984) documented
Chattah & Smith, 2006; Watson, 2008b). Erosion has this pattern of flatness of molar wear plane in
also been documented to play an important role in the comparisons of archaeological samples of food foragers
differential destruction of tooth surfaces with various to dedicated agriculturalists. These studies provide
diets (Kieser et al., 2001). Additional factors have been evidence for the correlation between molar occlusal
considered as potential secondary contributors to wear and subsistence, which has allowed researchers to
tooth wear including tooth form and structure, occlusal draw inferences about dietary behaviours of past
relationships, enamel quality, ingestion of grit and populations (e.g. Molnar, 1971; Smith, 1984; Larsen,
cultural activities such as the use of teeth as tools (Milner 1997; Kaifu, 1999; Chattah & Smith, 2006; Deter,
& Larsen, 1991; Sciulli, 1997). However, it has been 2009; Fujita & Ogura, 2009).
shown that dietary composition and food processing
methods have the greatest effect on patterns of occlusal
surface wear observed in archaeological samples The formative transition in the lower
(Molnar, 1971; Smith, 1984; Kieser, 1990; Larsen, Azapa Valley
1997; Sciulli, 1997; Kaifu, 1999; Hillson, 2002). The
application of these concepts has been particularly The Andes is one of the global centres of
successful in observing changes related to subsistence independent domestication (Smith, 1998; Pearsall,
and diet in prehistoric skeletal samples (e.g. Larsen, 2008), but the suite of domesticates that formed the
1981, 2002; Milner & Larsen, 1991; Lukacs, 1992; foundation of Formative cultures in the area include
Kieser et al., 2001; Chattah & Smith, 2006; Deter, 2009; both local species such as quinoa (Chenopodium quinoa),
Fujita & Ogura, 2009; Liu et al., 2010). potatoes (Solanum tuberosum, Tropaeolum tuberosum, Oxalis
Both wear rate and wear plane of the occlusal sur- tuberosa and Ullucus tuberosus), manioc (Manihot esculentum),
face show dramatic changes when human groups alter llama (Lama glama), alpaca (Lama pacos) and guinea pig
their food behaviours, in overall subsistence, consump- (Cavia porcellus and other species), and foreign species
tion or processing techniques (Molnar, 1971; Smith, from North America such as corn (Zea mays), beans
1972; Scott, 1979a, 1979b; Larsen, 1981; Smith, 1984; (Phaseolus vulgaris) and squash (Cucurbita pepo and other
Pechenkina et al., 2002; Chattah & Smith, 2006; Watson, species) (Smith, 1998). This is important to the
2008a). Molnar (1971) documented consistent differ- cultural development in South America because many
ences in wear rate between skeletal samples of food scholars have argued that foreign domesticates such
foragers and agriculturalists from North America. He as maize played a major role in stimulating the
suggested that because foraging groups consumed a development of early Andean civilization, such as at
wider variety of less processed foods than agricultural Chavin de Huantar (Mangelsdorf & Reeves, 1939;
groups, tough, fibrous diets caused powerful chewing Kidder, 1962; Kidder et al., 1963; Finucane, 2009). A
and extensive lateral movements of the jaw, producing great deal of the evidence for domestication of local
flat occlusal wear at relatively rapid rates. Reinhardt plant species and the arrival of foreign species
(1983) has shown that dietary consistency produces appears just prior to about 2000 BC throughout the
significantly enough force on the dental arch that it Andean region but would likely have been used in
can create zero to negative overjet (overbite) in groups various capacities well beforehand (Smith, 1998;
exhibiting heavy attrition. Pearsall, 2008).
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 289

Along much of the Andean coast, there is evidence that new resources and technologies into the primary
the first attempts by coastal residents to produce food are economic system.
accompanied by intensification in the exploitation of The Formative period (1500 BC–AD 500) in the lower
marine resources (Rivera et al., 1974; Focacci, 1980; Azapa Valley (Figure 1) is principally demarcated from
Rivera, 1984, 1991; Stanish, 2001; Muñoz, 2004; Arriaza the preceding Archaic period (8000–1500 BC) by the
& Standen, 2008; Pearsall, 2008; Finucane, 2009; cessation of artificial mummification as a typical burial
Watson et al., 2010). This new economic contribution practice, the appearance of sand‐tempered ceramics,
also perhaps produced intensification in meat and incipient agricultural production and pastoralism, and
wool for the manufacture of textiles (Kidder, 1962; the establishment of villages in the valley interior
Focacci, 1980; Santoro, 1980a, 1980b; Muñoz, 1981, (Focacci, 1974; Santoro, 1980a, 1980b, 1980c; Muñoz,
1983; Pearsall, 2008; Finucane, 2009). The incorpor- 1981, 1983, 1989, 2004). Previous settlements in the
ation of camelids into the economies of these groups is area, known as the Chinchorro culture, comprised
reflected in several cultural expressions, such as in approximately 6000 years of stable marine and some
textile motifs and in rock art of the region (Focacci, limited terrestrial foraging (Allison et al., 1984; Arriaza,
1980; Muñoz, 1989, 2004; Finucane, 2009). The 1994, 1995). Although there is evidence for continuous
period just prior to the formation of agricultural contact between the coast and altiplano throughout
villages and larger socio‐ceremonial centres along the prehistory (Rivera, 1984), the Chinchorro maintained a
central Andean coast demonstrates that the process sedentary lifestyle heavily reliant on the rich marine
was not a violent interruption of existing foraging resources that are available along the Pacific coast
adaptations in the region but instead fitted into a (Arriaza, 1994, 1995; Arriaza et al., 2005; Arriaza &
larger gradual process of cultural development and Standen, 2008). During the early part of the second
increasing complexity whereby the actors integrated millennium BC, groups along the coast began to

Figure 1. Location of sites in the lower Azapa Valley.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
290 J. T. Watson et al.

cultivate domesticated crops including quinoa, potato, the coast (Focacci & Erices, 1972–1973; Focacci, 1980).
manioc, corn, beans, squash and chillies (Muñoz, 2004). These sites also present considerable evidence for
Some of the populace relocated in the interior of the San exploitation of marine resources, especially shellfish;
José River valley and began practising animal husbandry but archaeological evidence indicates that the dietary
with domesticated camelids, such as llama and alpaca base focused equally on agro‐pastoral production and
(Muñoz, 2004). The beginning of the Formative period the exploitation of marsh resources along the river
therefore represents a major shift in subsistence strategy (Santoro, 1980a, 1980b, 1980c; Muñoz, 1981, 1983,
from that practised by the area’s previous inhabitants. 1989, 2004; Watson et al., 2010).
Formative period sites in the lower Azapa Valley can The Formative period can additionally be divided
be separated into two groups based on location: coastal into concurrent archaeological phases at both loca-
and valley interior sites. Coastal sites (Playa Miller‐7 tions in the lower Azapa Valley. The early phase
and Quiani‐7—Figure 1; Camarones‐15—Figure 2) are (1500–500 BC) is termed Faldas de Morro in coastal
located directly adjacent to the shoreline and close to sites (Dauelsberg, 1963) and Azapa in valley sites
the marshy mouths of the San José and Camarones (Santoro, 1980b). The late phase (500 BC–AD 500) is
rivers (Focacci, 1974, 1980). Although evidence for termed El Laucho in coastal sites (Focacci, 1974) and
cultigens and low level agro‐pastoral investment is Alto Ramirez in valley sites (Santoro, 1980b). Subtle
plentiful, the dietary base focused on exploitation of differences in artefact assemblages define the arch-
readily accessible marine resources (Muñoz et al., 1991; aeological phases, but they are basically analytical
Watson et al., 2010). Valley interior sites (Azapa‐14, tools used to highlight variability observed in the
70, 71 and 75—Figure 1) are located adjacent to the archaeological record (Arriaza & Standen, 2008).
San José River floodplain approximately 12 km from Material culture recovered from these sites is similar

Figure 2. Location of the Camarones‐15 site in lower Camarones Valley.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 291

in the broader sense that cultigens and items interior (p < 0.05). These percentages reflect the
representing agricultural technology are present in frequency or ‘observed rate’ [caries rates were corrected
both areas (Rivera, 1984, 1991). Although differ- using Lukacs' (1995) formula to account for tooth
ences are present, they are minor compared with loss], which describe the percentage of teeth or
the unmistakable impact the arrival of domesti- alveolar segments affected and are calculated by
cated cultigens had on subsistence strategy, as ob- dividing the number of carious or missing teeth by
served in the archaeobotanical record of these sites the total number of locations observed.
(Muñoz, 2004). Although the archaeological evidence indicates that
Several scholars suggest that the Formative transi- both groups practised a shared mixed subsistence
tion in the lower Azapa Valley is the result of demic economy, residents along the coast placed greater
diffusion of highland agriculturalists into the area investment in foraging marine resources whereas
(Santoro, 1980b; Rothhammer et al., 1982, 2002; residents in the valley placed greater investment in
Muñoz, 1983, 1989). They often cite the appearance agro‐pastoral production. We concluded that these
of altiplano ceramics and textile motifs during the patterns reflect niche construction and differences in
Formative period to support the conclusion that the dietary base between the coast and valley interior
agro‐pastoralist subsistence strategy was brought in by (Watson et al., 2010). This pattern of differential
migrants from the cordillera (Rivera, 1984, 1991; investment could also produce measurable variability
Varela & Cocilovo, 2002). If this were the case, one in tooth wear and further affect patterns of oral
would expect to find greater archaeological differences disease observed in the samples. Here, we examine
between contemporaneous coastal and valley interior occlusal surface wear in the same skeletal samples of
sites, and the evidence for mixed subsistence practices incipient agriculturalists from the lower Azapa Valley
from both locations would be somewhat counter- to test the hypothesis that, concomitant with
intuitive. Other researchers document continuous differences observed in oral pathology, in coastal
cultural and biological continuity in the lower Azapa groups consuming a greater percentage of foraged
Valley (Sutter, 1997, 1999, 2000, 2005a, 2005b, 2006; foods, occlusal surfaces should wear faster and exhibit
Rothhammer & Santoro, 2001). Most of Sutter’s work flat molar wear plane angles, whereas among valley
with the Azapa Valley samples has involved defining interior groups consuming a greater percentage of
local, regional and temporal genetic distances using agro‐pastoral products, these should wear slower but
discrete dental traits (Sutter, 1997, 1999, 2000, 2005a, exhibit more angled molar wear.
2005b, 2006; Sutter & Mertz, 2004). In every case, his
results demonstrate genetic continuity within groups of
the lower valley, a pattern that generally persists Materials
through time (Sutter, 1997).
In a recent related study, we identified that markers The skeletal samples analysed for this study are part of
of oral health varied significantly by site location but the osteological collection held in repository at the
not by archaeological phase during the Formative Universidad de Tarapaca Museo Arqueológico de San
period in the lower Azapa Valley (Watson et al., 2010). Miguel de Azapa, Arica, Chile. We examined maxillary
Fewer caries (3.8%) and lost teeth (9.6%) were and mandibular dentition from crania of 200 adult
observed in skeletal samples from the coast, whereas individuals (age ≥ 15 years) from seven Formative
numerous caries (19.7%) and more lost teeth (13.4%) period sites (Table 1) in the lower Azapa Valley
were observed in skeletal samples from the valley (Figure 1) and one contemporaneous site from the

Table 1. Skeletal sample from lower Azapa Valley

Site N Location Phase (culture)

AZ‐14 30 Valley Late (Alto Ramirez)


AZ‐70 25 Valley Late (Alto Ramirez)
AZ‐71 5 Valley Early (Azapa)
AZ‐71 18 Valley Late (Alto Ramirez)
AZ‐75 27 Valley Late (Alto Ramirez)
CAM‐15 11 Coast Early (Faldas de Morro)
PLM‐7 80 Coast Late (El Laucho)
QUIANI‐7 4 Coast Early (Faldas de Morro)

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
292 J. T. Watson et al.

Camarones Valley coast (Figure 2) in northern Chile. adult subsamples between the coast and valley
Eleven individuals from the Camarones‐15 site were interior locations, and between early and late
added to the coastal sample to bolster the limited archaeological phases, were significant at the 5%
number of individuals dating to the early phase. level. Given that attrition is principally associated
Biological and archaeological variables all suggested a with age and the duration a given tooth is in
shared history and connection between the Azapa and occlusion, it is therefore important that we control
Camarones Valley residents prior to, and during, the for age in the analyses that follow.
Formative period (Muñoz, 1989, 2004; Muñoz et al.,
1991; Arriaza & Standen, 2008). The dental sample
consists of a total of 1268 teeth. Preservation of the Methods
dentition is generally excellent; however, a number of
individuals were missing teeth because of postmortem Three analyses were conducted on the dental sample
loss. Pearson chi‐square cross‐tabulations identify that from the lower Azapa Valley comparing attrition by
the distribution of teeth does not differ significantly location and archaeological phase in order to test the
between coast and valley interior locations central hypothesis that in coastal groups consuming
(χ2 = 13.252, df = 15, p = 0.583) or between the early greater quantities of foraged foods, occlusal surfaces
and late archaeological phase (χ2 = 6.050, df = 15, should wear faster and exhibit flat molar wear,
p = 0.979). whereas among valley interior groups consuming
Sex was estimated for individuals in the sample by greater quantities of agro‐pastoral products, these
examining standard macroscopic aspects of the pelvis should wear slower but exhibit more angled molar
and/or cranium (Buikstra & Ubelaker, 1994). The sample wear. These analyses included comparisons of (i) raw
is comprised of relatively even numbers of men (n = 101) average wear, (ii) molar wear rate and (iii) molar wear
and women (n = 99). Age was estimated for the sample angle.
using dental eruption (after Ubelaker, 1978), epiphyseal
fusion, cranial suture closure and macroscopic degen- Raw average wear
erative changes in the pubic symphysis following
standards described by Buikstra & Ubelaker (1994). Raw average wear scores were compared for each tooth
The sample was classified into four ordinal 9‐year age using independent samples t‐tests to identify if gross
cohorts (15–24, 25–34, 35–44, 45–54 years). Individuals differences in wear exist across the dentition. This is a
assigned to the oldest age group generally had the measure of the amount of wear on each tooth and can
most severe attrition, were more often affected by be used for a general comparison to identify if
tooth loss or damage resulting in uneven wear and differences in the amount of wear exist between
therefore were eliminated from the sample. Miles samples and which teeth specifically exhibit these
(2001) identified that age estimation using attrition differences. Heavy wear (significant loss of the crown)
scores tends to underestimate older individuals in is more commonly associated with groups practising a
skeletal samples and coincides with greater tooth loss. dedicated foraging economy and is often found to be
Most relevant to this study is the fact that extreme greatest on the anterior teeth (anterior loading),
wear that compromises the integrity of the crown and whereas dedicated agriculturalists often exhibit lighter
crosses the cemento‐enamel junction results in faster, or more variable wear in general, yet the heaviest wear
more unpredictable wear than in earlier stages or is often associated with the posterior teeth among
younger individuals (Miles, 2001; Hillson, 2002). agriculturalists (Molnar, 1971; Reinhardt, 1983; Smith,
Teeth exhibiting severe dental pathology or extreme 1984; Milner & Larsen, 1991; Kaifu, 1999; Deter, 2009).
wear (incisor, canine, premolar: wear scores >8; molar: Occlusal surface wear was recorded for both sides of
wear scores >32), resulting in loss of crown integrity, adult maxillary and mandibular dentition in the
and teeth with opposing occlusal teeth missing sample, but only the left side was used in the
antemortem were therefore eliminated from analysis. analyses. Occlusal wear was scored using ordinal
This additionally functioned to eliminate numerous scales following Smith (1984) for incisor, canine and
teeth representing the oldest individuals in the premolar teeth and following Scott (1979a) for molar
sample and resulted in an equal distribution of the teeth. No significant differences in wear rate were
sample between the remaining three adult age observed between right and left dentitions using
groups (χ2 = 2.583, df = 2, p = 0.275). However, paired‐samples t‐test; therefore, if a tooth was missing
two‐tailed Mann–Whitney U‐tests showed that the from the left side, the antimere was used to facilitate
differences in the estimated age compositions of the a larger comparative sample size.
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 293

Molar wear rate to wear rates of left mandibular M1 and M2 between


coast and valley interior sites and between early and
A subsample of 112 paired first (M1) and second (M2) late archaeological phases within the lower Azapa
mandibular molars (n = 224) was selected to assess rate Valley sample.
and angle of occlusal surface wear using attrition scores
between site locations and archaeological phases. Total Molar wear angle
wear scores were compared between paired molars
using principle axis analysis to identify if the rate of Summed wear scores were compared between buccal
wear differed. This test is designed to measure the rate cusps of the first molar (M1) and lingual cusps of the
(or speed) of occlusal surface wear exerted on the second molar (M2) using principle axis analysis
molars and identify if differences exist in how fast following Chattah & Smith (2006) to identify if the
molars wear on average between samples. Faster rates angle of occlusal wear differed between locations or
of molar wear are often associated with harder diets archaeological phases. This test is designed to measure
resulting from foraging wild foods and minimal the angle of occlusal surface wear exerted on the molars
processing, whereas slower although more variable and to identify if differences exist in how molars wear on
rates of wear are more commonly associated with average between samples. The development of the
softer diets and the consumption of agricultural occlusal surface wear plane, or angle, is largely the result
products such as domesticated cultigens, which are of the juxtaposition of hard versus soft diets and the
often heavily processed (Smith, 1982, 1984; Larsen, consistency of foods consumed regularly. Flat molar
1997; Lukacs, 1996; Sciulli, 1997; Kieser et al., 2001; wear angles are often the result of harder diets associated
Fujita & Ogura, 2009). with foraging wild foods and minimal processing,
Occlusal wear was scored on each quadrant of the whereas steeper molar wear angles are often the result
molar surface using the 10‐point ordinal scale devel- of softer diets and increased tooth‐on‐tooth contact
oped by Scott (1979a). In this method, each of the associated with the consumption of agricultural prod-
four molar surface quadrants is given a wear score ucts that are often heavily processed (Molnar, 1971;
ranging between 1 and 10 based on relative enamel Scott, 1979b; Smith, 1984; Chattah & Smith, 2006;
loss. Scores for all four quadrants are added to give the Watson, 2008b; Deter, 2009; Fujita & Ogura, 2009).
overall wear score for the tooth, ranging from 4 to 40. This methodology is a further modification of
Smith (1972) proposed the use of a method modified Scott’s (1979b) approach and has the advantage of
from Miles (1963, 2001) to determine wear rate in comparing both the rate and angle of molar occlusal
skeletal samples that avoids the problems of age surface wear. It employs the functional differential in
dependency inherent with dental attrition. Smith wear based on order and timing of eruption between
(1972) used correlation and regression analysis to M1 and M2 and measures the differential in wear rate
compare the differences in wear between the paired between paired buccal versus lingual cusps. The
first and second molars, utilising the staggered potential exists to underestimate the degree of wear
approximate 6‐year interval timing of molar eruption angle in younger individuals where M2 exhibits
as a proxy for age. As all of the teeth used from the minimal wear; however, this also makes the test robust
sample represent adult individuals, Smith’s (1972) and less susceptible to the affects of idiosyncratic wear
system provides an age‐independent assessment of on M1. This technique was also chosen because of its
wear rates. flexibility, ease of application and comparability in the
Scott (1979b) further built upon Smith’s (1972) place of more technically complex or time‐consuming
approach and proposed the use of principle axis techniques such as morphometric (i.e. Bailey, 2004) or
analysis and successfully demonstrated that the slope three‐dimensional surface or image analysis (i.e.
of the principle axis equation could be used as an Mayhall & Kageyama, 1997). More specifically, these
indicator of the rate of wear, whereby a steeper slope results are directly comparable with that of similar
indicates a rapid rate of wear. Although interval data studies in other regions of the world that have
would be preferable for statistical treatment, Benfer & considered the effects of dietary changes associated
Edwards (1991) were able to demonstrate that results with the introduction of agriculture using wear rates
of principle axis analyses using the Scott scoring and planes (Molnar, 1971; Smith, 1984; Pechenkina
system are similar to those produced using measure- et al., 2002; Chattah & Smith, 2006; Watson, 2008b;
ments of crown height and suggest that it is therefore Deter, 2009).
an effective tool for assessing rates of occlusal surface Principal axis analysis was employed in the last two
wear. Principal axis analysis (Scott, 1979b) was applied analyses because it does not assume a causal relationship
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
294 J. T. Watson et al.

between variables and does not assume that the X‐axis is differential loading on the posterior teeth among
uniformly measured without error (Scott, 1979b; coastal residents. However, most prehistoric foraging
Chattah & Smith, 2006). Bivariate normality (p > 0.10) populations present differential loading in the anterior
was found for all subsamples. In comparing wear rate, dentition, much of which is commonly associated with
the principal axis equation was determined by the non‐masticatory use of anterior teeth, such as
plotting the wear score of M1 on the Y‐axis and grasping fibres (Molnar, 1971; Reinhardt, 1983; Smith,
M2 on the X‐axis. For the comparison of wear plane, 1984; Milner & Larsen, 1991; Kaifu, 1999; Deter,
the principal axis equation was determined by 2009). The pattern of posterior loading observed in the
plotting the wear score of the M1 buccal surface on coastal samples may reflect a difference in the specific
the Y‐axis and the wear score of the M2 lingual foraged resources consumed (i.e. marine resources) or
surface on the X‐axis. A steeper principal axis slope in processing techniques compared with other groups
(b) indicates a faster wear rate or steeper wear plane principally invested in foraging, specifically compared
angle. Following Scott (1979b), bivariate plots of the with terrestrial foragers.
data were prepared. When the samples were pooled across locations and
Intra‐observer error was assessed by repeating compared by archaeological phase, raw average wear
analysis on 30 random dentitions 4 months after the scores were generally higher in the early phase, with
originals were conducted. The mean difference in wear differences in wear on three posterior maxillary teeth
scores of the occlusal surface was two (standard (UP1, UP2, UM2) and four mandibular teeth (LC,
deviation of 2). In each case, error variances were less LP1, LP2, LM2) being statistically significant. Despite
than 10% of total observed variation, confirming that smaller sample sizes, and although attrition scores vary
they were small and unlikely to bias results. All across more teeth by archaeological phase, to some
statistical tests were performed using the SPSS 14.0 for extent the pattern is indicative of greater total wear at
Windows programme (Statistical Package for Social the beginning of the Formative period in the lower
Sciences, Chicago, IL). Azapa Valley. Other studies of dental attrition and
subsistence patterns typically associate greater overall
wear with foraging and limited processing of consumed
Results resources (Smith 1982, 1984; Sciulli, 1997; Kieser et al.,
2001; Deter, 2009; Fujita & Ogura, 2009). The pattern
Raw average wear of greater overall wear observed during the early phase
may reflect greater investment in foraging resources at
Tables 2 and 3 summarise descriptive statistics and the beginning of the Formative period, which
hypotheses tests for attrition scores of left maxillary eventually gave way to a more balanced, mixed
and mandibular dentitions. The t‐test comparisons subsistence economy.
identify several teeth for which attrition differs
significantly between subsamples. Wear scores were Molar wear rate
higher on average among coastal residents, but only
the molars (UM1, UM2, UM3, LM2 and LM3) Table 4 shows the results of the principle axis analyses
demonstrated statistically significant differences. This on paired left mandibular molar wear scores. The rate of
pattern of greater wear on the molars is indicative of average molar occlusal surface wear, as measured on M1

Table 2. Descriptive statistics and t‐tests for left maxillary attrition by site location and archaeological phase

Coast Valley p‐value Early Late p‐value

n Mean SD n Mean SD n Mean SD n Mean SD

UI1 16 3.63 1.20 30 3.50 1.33 0.756 9 3.56 1.33 36 3.56 1.30 0.999
UI2 21 3.48 1.12 36 3.78 1.46 0.418 10 3.40 1.26 47 3.72 1.36 0.493
UC 37 3.54 1.22 51 3.57 1.53 0.926 11 3.82 1.40 77 3.52 1.40 0.510
UP1 42 3.90 1.39 53 3.64 1.73 0.426 12 4.75 1.54 83 3.61 1.55 0.020*
UP2 46 3.89 1.35 57 3.86 1.72 0.919 12 4.75 1.48 91 3.76 1.54 0.037*
UM1 59 5.83 1.54 61 5.02 1.47 0.004* 12 5.94 1.54 108 5.36 1.55 0.223
UM2 56 4.93 1.50 65 3.63 1.34 0.001* 14 5.13 1.80 107 4.11 1.49 0.021*
UM3 30 3.83 1.16 43 2.28 1.23 0.001* 9 3.47 1.16 64 2.84 1.44 0.213

*Significant at the 0.05 level.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 295

Table 3. Descriptive statistics and t‐tests for left mandibular attrition by site location and archaeological phase

Coast Valley p‐value Early Late p‐value

n Mean SD n Mean SD n Mean SD n Mean SD

LI1 15 3.87 1.06 27 3.96 1.81 0.851 5 4.60 1.67 37 3.84 1.55 0.314
LI2 18 4.28 1.36 33 3.79 1.47 0.250 6 4.83 0.98 45 3.84 1.46 0.115
LC 27 3.96 1.13 36 3.69 1.39 0.415 8 4.75 1.04 55 3.67 1.26 0.025*
LP1 39 4.00 1.24 42 3.81 1.70 0.568 10 5.00 0.94 71 3.75 1.49 0.012*
LP2 38 4.03 1.26 49 3.67 1.52 0.251 10 5.00 1.15 77 3.68 1.38 0.005*
LM1 41 5.71 1.31 40 5.20 1.41 0.098 10 6.25 1.34 71 5.35 1.35 0.051
LM2 45 4.85 1.48 40 4.00 1.53 0.011* 11 6.00 1.50 74 4.22 1.43 0.001*
LM3 38 3.60 1.17 37 2.95 1.38 0.032* 6 3.46 1.08 69 3.26 1.34 0.732

*Significant at the 0.05 level.

against M2, mirrors those trends observed in attrition Molar wear angle
scores between locations. Residents of the coastal sites
had a steeper principle axis slope compared with those Wear was greater on the molar buccal cusps in groups
from valley interior sites (Figure 3(a)) indicating a for all comparisons (Table 4). Principle axis analysis of
slightly faster rate of wear; however, the difference was M1 buccal cusps wear scores against M2 lingual cusps
not statistically significant (p > 0.05). A faster rate of wear scores demonstrate a steeper principle axis slope
wear is consistent with other studies of dental attrition and therefore a greater occlusal wear angle in molars
among prehistoric foraging groups (Smith 1982, 1984; from coastal sites (Figure 4(a)). There is considerable
Walker & Erlandson, 1986; Larsen, 1997; Lukacs, 1996; variability in the wear plane angles of both coastal and
Sciulli, 1997; Kieser et al., 2001; Deter, 2009; Fujita & valley interior residents; therefore, the difference in
Ogura, 2009) and, although non‐significant, may slope by site location is not statistically significant
reinforce the results observed in the raw average wear (p > 0.05). However, it is interesting that the molar
scores. wear angle is steeper among the coastal group because
When samples were pooled across locations and most studies of attrition patterns associate flat molar
compared by archaeological phase, the early phase wear with foraging and limited processing of consumed
displayed a slightly higher, but non‐significant, rate of foods compared with more angled molar wear among
wear when compared with that of the late phase agriculturalists consuming softer, more processed diets
(Figure 3(b)). This pattern also matches the greater (Smith 1982, 1984; Larsen, 1997; Sciulli, 1997; Kieser
overall wear observed in the raw average scores et al., 2001; Watson, 2008b; Deter, 2009; Fujita &
observed in the early‐phase samples and suggests that Ogura, 2009). Although non‐significant, the pattern
although the rate of wear may be similar over time, it is observed here is suggestive of dissimilarity in dietary
generally greater early in the cultural sequence. Again, consistency among the coastal foragers of the lower
although non‐significant, a faster rate of wear is mostly Azapa Valley compared with terrestrial foragers in
seen among foraging groups that consume a minimally other parts of the globe.
processed diet and therefore could be indicative of The principle axis analysis also demonstrated a
greater investment in foraging resources during the steeper slope and therefore greater occlusal wear angle
early phase in the lower Azapa Valley. in molars associated with the early phase (Figure 4(b))

Table 4. Principle axis slope (b), equation and 95% confidence limits

b Principle axis equation CL (95%)

Coast M1 vs M2 0.726 2.499 + 0.726y 0.487 < b < 0.966


Valley M1 vs M2 0.664 2.492 + 0.644y 0.446 < b < 0.882
Early M1 vs M2 0.745 2.977 + 0.745y 0.246 < b < 1.244
Late M1 vs M2 0.683 2.476 + 0.683y 0.520 < b < 0.846
Coast M1 buccal vs M2 lingual 0.809 6.676 + 0.809y 0.481 < b < 1.138
Valley M1 buccal vs M2 lingual 0.613 7.557 + 0.613y 0.367 < b < 0.859
Early M1 buccal vs M2 lingual 1.050 5.842 + 1.050y 0.216 < b < 2.190
Late M1 buccal vs M2 lingual 0.662 7.363 + 0.662y 0.472 < b < 0.852

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
296 J. T. Watson et al.

among the coastal residents. Steeper molar wear during


the early phase may instead be interpreted to indicate a
difference in dietary consistency compared with other
foraging groups, specifically compared with terrestrial
foragers.
The limited sample size for the early phase,
particularly from the valley interior (n = 5), could
contribute to the results obtained here, whereby
heavier wear, experienced by coastal foragers during
the early phase, could be masked when pooled with
later‐phase coastal samples but reflect a stronger signal
over the valley interior sample of the early phase.
Unfortunately, sample sizes are too small to compare
early‐phase with late‐phase coastal samples and early‐
phase with late‐phase valley interior samples. However,
given that sample sizes are somewhat limited,

Figure 3. (a) Scatterplot of average wear scores of M1 and M2


by site location, shown with regression lines. (b) Scatterplot of
average wear scores of M1 and M2 by archaeological phase,
shown with regression lines.

in the lower Azapa Valley. Although similar variability


can be observed in early‐phase and late‐phase group-
ings, the respective principle axis slopes are sufficiently
dispersed from each other to be statistically significant
(p < 0.05). As mentioned above, steeper molar wear
planes are principally associated with an agricultural
lifestyle and a softer, more processed diet (Smith,
1984; Sciulli, 1997; Deter, 2009). If the patterns
observed in this study reflect similar adaptations, then
one could conclude that the residents of the lower
Azapa Valley were heavily invested in domesticated
products or were heavily processing foods at the
beginning of the Formative period but reverted to
utilise more foraged resources or limited processing Figure 4. (a) Scatterplot of M1 buccal cusps and M2 lingual
during the late phase. This seems like an unlikely cusps wear scores by site location, shown with regression lines.
(b) Scatterplot of M1 buccal cusps and M2 lingual cusps wear
interpretation given heavier wear and slightly faster scores by archaeological phase, shown with regression lines.
rates and angles during both the early phase and Note steeper slope for early‐phase subsample.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 297

particularly for the early phase, those differences from the valley interior is the result of destruction by a
observed in attrition that are statistically significant carious lesion.
are likely strong and therefore meaningful.
Figure 5 shows a typical pattern of wear common
among Formative period coastal groups versus valley Discussion
interior groups in the lower Azapa Valley. The figure
illustrates those patterns observed in the data: heavy In a recent related study, we identified higher
posterior wear, at a relatively faster rate and with a frequencies of caries and lost teeth among samples
slightly steeper molar occlusal angle at coastal sites, from the valley interior and subsequently proposed
compared with overall less severe wear, at a slower rate that this differential expression of oral pathology in
and with more cupped, but less angled, molar occlusal closely related groups was likely the result of greater
surface wear at valley interior sites. These patterns also investment in agro‐pastoral resources and niche
hold true—and are statistically significant—during the construction by residents of the valley interior
early phase. An additional phenomenon that was (Watson et al., 2010). This conclusion formulated the
observed to differ between locations was an extensive original impetus for this investigation, and we tested
amount of chipping (damage) to dental crowns among the hypothesis here that, concomitant with differences
the coastal residents (37.9%) compared with those observed in oral pathology, in coastal groups consum-
from the valley interior (5%; p < 0.001). Damage to the ing a greater percentage of foraged foods, occlusal
crown can further exacerbate differential wear, espe- surfaces would have worn faster and exhibit flat molar
cially between molar surfaces (Scott & Winn, 2011). wear, whereas among valley interior groups consuming
Enamel chipping was recorded as part of the larger a greater percentage of agro‐pastoral products, these
dental analysis by simply counting the number of chips would have worn slower but exhibit more angled molar
present that were clearly antemortem (those with some wear. The results of our analyses demonstrated greater
wear on the edges of the damaged surface compared average tooth wear among coastal residents but limited
with sharp edges likely due to postmortem damage). differences (not statistically significant) in rates of
Chipping of the crown can be observed on the lingual attrition and wear angle in the molars compared with
edge of the lingual–distal cusp of M1 in Figure 5. In that of the residents of the valley interior. Although we
addition, the figure displays exposure of the pulp identified some differences in wear, we reject our
cavity in a molar from both dentitions; however, the hypothesis, with some caveats, that molar wear rate
exposure in the individual from the coast is the result and angle demonstrated significant differences by
of heavy wear, whereas the exposure in the individual location (coast vs valley interior). Instead, we found
significantly greater average wear and steeper molar
wear angles and a minimally faster wear rate (not
statistically significant) in dentitions from the early
phase of the Formative period.
Two important patterns were therefore identified
from the analyses conducted on the dental sample from
the lower Azapa Valley: (i) coastal residents exhibited
differential loading on the posterior dentition; and (ii)
dentition from the early phase exhibited greater average
wear over the dental arch and steeper molar wear angles.
Archaeological evidence (Dauelsberg, 1963, 1974;
Muñoz & Chacama, 1982; Muñoz, 1989, 2004; Muñoz
et al., 1991; Arriaza & Standen, 2008) and patterns of oral
disease (Watson et al., 2010) indicated that the residents
of the coast continued to principally invest in marine
foraging throughout the Formative period. In addition,
the limited sample of early‐phase individuals from the
Figure 5. Photo of right mandibular posterior teeth highlighting
valley interior sites basically creates a ‘coastal’ signature
wear and damage typical of Formative period sites in the lower for the subsample, one largely based on foraging marine
Azapa Valley. Top is of a 35‐ to 45‐year‐old man from the late‐ resources. Therefore, the significant patterns of attrition
phase coastal site of Playa Miller‐7 (individual CR‐133). Bottom
is of a 30‐ to 40‐year‐old man from the late‐phase valley site of observed in both the coastal and early‐phase samples
Azapa‐75 (individual T‐123). can principally be attributed to a marine‐based diet.
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
298 J. T. Watson et al.

This is significant because our results are partially provide almost no resistance and promote contact
opposed to patterns observed in most studies of dental between opposing tooth surfaces. In addition, grit and
attrition among foraging groups, which are attributed to using teeth for processing hard components of the diet
anterior loading, heavy overall wear and flat wear molar such as shells and fish bones can contribute to damage
wear planes. of the tooth crown and enamel chipping (Scott &
Differences in occlusal surface wear have been shown Winn, 2011) as also demonstrated to be more
to generally correspond with subsistence practices common among the coastal residents of the lower
among pre‐industrial populations (Molnar, 1971; Smith, Azapa Valley.
1984; Larsen, 1997; Kaifu, 1999; Kieser et al., 2001; Another possible explanation for the patterns of
Deter, 2009; Fujita & Ogura, 2009; Liu et al., 2010). The tooth wear observed in the lower Azapa Valley samples
observation that coastal groups exhibit more extensive could lie in the integration of agricultural products and
posterior tooth wear lends support, at least superficially, food processing technology that accompanied the
to dietary specialisation and the premise that coastal beginning of the Formative period in the region. The
groups were more heavily invested in marine foraging. addition of domesticated cultigens to existing foraging
However, most studies identify that foragers exhibit subsistence strategies increased carbohydrate consump-
greater anterior tooth wear relative to molar wear tion and created an increase, although minor, in the
compared with agricultural groups (Molnar, 1971; incidence of caries compared with the preceding coastal
Smith, 1984; Kaifu, 1999; Deter, 2009), the reverse of Archaic groups (Kelley et al., 1991; Watson et al., 2010).
what was observed in the coastal samples examined in The relationship between dental caries and tooth wear is
this study. Greater anterior loading is commonly still unclear, but Larsen (1997) suggested that groups
associated with using the front teeth for tool fabrication with high attrition rates often have low caries rates.
among foragers (Macchiarelli, 1989; Larsen, 1997), but Hillson (2002) was more cautious and advised that this
the Azapa coastal sample lacks heavy anterior wear and does not necessarily indicate a causal relationship.
evidence of task‐specific wear. Populations with heavy attrition have been shown to
Heavier and flatter tooth wear is also fundamentally maintain greater frequencies of cervical caries, an area
associated with the particularly tough nature of that attrition is less likely to effect. This was not found
consuming minimally processed foraged resources to be the case in the lower Azapa Valley where the
(Molnar, 1971; Smith, 1984; Larsen, 1997; Deter, residents of the valley interior had significantly higher
2009). Our results not only certainly identified heavier rates of cervical caries than the residents adjacent to
wear among the residents of the coast from the lower the coast (Watson et al., 2010). Occlusal attrition has
Azapa Valley (similarly for the early phase) but also the potential to remove fissure caries, but the normal
determined that they exhibited steeper molar wear progression of fissure lesions is rapid and attrition can
angles more similar to agricultural groups consuming a often do little to prevent them. Although the
soft, heavily processed diet, largely the result of greater relationship between dental disease and tooth wear
tooth‐on‐tooth contact. Unlike tougher fibrous diets is still unclear, the possibility does exist that a change
common to terrestrial foragers, foraging aquatic in dietary proportions could have functioned to
resources (Yesner, 1980) has been shown to create similarly alter wear patterns among the residents of
variable, less predictable patterns of tooth wear the lower Azapa Valley, particularly with those living
(Walker & Erlandson, 1986; Macchiarelli, 1989; along the coast.
Littleton & Frohlich, 1993). The patterns of dental In a study of oral pathology and dental attrition in
attrition observed in coastal samples (and early phase) prehistoric groups along the Arabian coast, Littleton
in the lower Azapa Valley samples are similar to those & Frohlich (1993) identified distinctive patterns
documented among coastal groups in other parts of the among groups practising mixed subsistence econo-
world (Walker & Erlandson, 1986; Macchiarelli, 1989; mies. These were additionally unique from patterns
Littleton & Frohlich, 1993). observed in dedicated coastal foragers and later
We propose that a marine diet can be a variably intensive farmers. They noted (i) high–moderate
tough—or simultaneously soft and gritty—and can rates of attrition, calculus and abscesses, and low rates
lead to more unpredictable tooth wear including heavy of caries and antemortem tooth loss among mixed
wear, at variable rates, and greater molar wear angles fisher–agro‐pastoralists; and (ii) low–moderate rates of
(Macchiarelli, 1989; Littleton & Frohlich, 1993). For attrition and high rates of caries, calculus and abscesses
example, crustaceans, shell fish and meat from sea with severe antemortem tooth loss among mixed fisher–
mammals provide considerable resistance during farming populations (Littleton & Frohlich, 1993). In both
mastication, whereas meat from fish and sea urchin cases, the practice of a mixed subsistence economy
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 299

resulted in reduced and more variable attrition the only location in the Americas where these
compared with the dedicated fishers. It is most circumstances occur. The remaining shoreline of the
interesting that the pattern observed among Arabian Americas lacked investment in pastoralism. It is also
fisher–agro‐pastoralists closely mirrors that observed likely that the interplay of investment in these varied
among the fisher–agro‐pastoralists of the Formative resources changed over the course of the Formative
period in the lower Azapa Valley (Watson et al., 2010). period, and as control over, and of, these resources (old
Changes in subsistence technology, such as the and new) stabilised, groups in the lower Azapa Valley
introduction and use of ceramics, as well as dietary canalised production roles in their respective niches by
composition could have played an equally important the later phase.
role in altering wear patterns during the Formative
period along the coast. Crude ceramic vessels are
introduced relatively early in the Formative period Conclusions
along with the suite of domesticates (Rivera et al.,
1974; Santoro, 1980b, 1980c; Muñoz, 1989, 2004; This study used wear scores from 200 Formative period
Rivera, 1991). New technology in food processing individuals from the lower Azapa Valley along the
using ceramic vessels, even within the confines of northern Chilean coast to test the hypothesis that,
marine foraging, would certainly affect grit content concomitant with differences in dental pathology,
and food consistency. Mølleson et al. (1993) and occlusal surfaces would wear faster and exhibit flat
Sciulli (1997) found that dental wear rates declined molar wear in coastal groups consuming greater
markedly with the development of ceramic cooking quantities of foraged foods, compared with slower
vessels. The use of ceramic vessels for cooking wear rates but more angled molar wear among valley
dramatically decreases food consistency and causes interior groups consuming greater quantities of agro‐
more tooth‐on‐tooth contact that functions to create pastoral products. Differences in overall wear patterns
steeper molar occlusal surface wear planes, such as between coastal and valley interior locations and in
those observed in the early phase of the lower Azapa molar wear plane were observed between the early and
Valley. However, it is curious that the angle decreases late archaeological phases. Traditional explanatory
in the samples over the course of the Formative period. models failed to encompass the multidimensional
Although the introduction of ceramic vessels may be a patterning identified in the data. Initially, the results
contributing factor to the wear patterns observed here, do not appear to support significant differences in
greater investment in foraging marine resources along tooth wear by site location, and we reject our
the coast, as is likely the case among the early‐phase hypothesis. However, these results are significant
samples, appears to be a more parsimonious explan- because they indicate a great deal of complexity to
ation in this case. the interaction between tooth wear, dental disease and
The variability in patterns of dental wear observed diet, particularly among groups that regularly exploit
among the residents of the lower Azapa Valley appears marine resources.
to fundamentally be the result of an extremely dynamic People living along the Andean coast practised
subsistence adaptation. The variable consistency of a stable marine foraging for several thousand years prior
marine diet, perhaps in conjunction with changes in to and after the Formative transition. However, the
food processing (i.e. the introduction of ceramic introduction of agriculture added new dimensions and
cooking vessels), could have produced the heavy wear resources for exploitation in existing subsistence
and steep molar occlusal surface angles observed systems. There are clear links between coastal and
among the coastal and early‐phase residents of the valley interior groups, with little distinction for the
area. The introduction and investment in domesticated duration of the Formative period. Both groups
cultigens and animals, while still maintaining a practised a mixed subsistence economy, utilising the
considerable degree of reliance on marine resources rich marine resources along the coast and investing in
as suggested by bioarchaeological data, could have agro‐pastoral production in the fertile river valleys.
limited wear rate and angle among residents of the Here, we argue that the nuances of tooth wear
valley interior (and the late phase) while simulta- observed in the data result from the variability inherent
neously creating more dental decay. What is most in a marine foraging diet and the incorporation of a
likely in both cases is that the variability in wear more inclusive mixed subsistence adaptation. Moreover,
observed among these groups can be specifically related the appearance and use of pottery among coastal groups
to the amalgamation of a marine–agro‐pastoral econo- could have played an additional significant role in
my. It is important to also note that the Andean coast is affecting patterns of wear in these samples.
Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
300 J. T. Watson et al.

Acknowledgements Childe VG. 1925. The Dawn of European Civilization. Kegan


Paul: London.
This work was supported by the William J. Fulbright Cohen MN, Armelagos GJ (eds.). 1984. Paleopathology at the
Origins of Agriculture. Academic Press: Orlando.
Visiting Scholar Grant, the Commission for the
Cohen MN, Crane‐Kramer GMM. 2007. Ancient Health:
International Exchange of Scholars, the Fulbright Skeletal Indicators of Agricultural and Economic Intensification.
Commission Chile, the Universidad Tarapaca de Arica University Press of Florida: Gainesville.
and the Museo Arqueológico San Miguel de Azapa. Dauelsberg P. 1963. Complejo arqueológico Faldas de
Study of the collections from Azapa was conducted Morro. Actas del 2º Congreso de Arqueología. San Pedro de
under the auspices of the project ‘Túmulos funerarios: Atacama.
Monumentos del paisaje desértico indicadores de la Dauelsberg P. 1974. Excavaciones arqueologicas en Quiani.
organización territorial de las poblaciones Formativas Chungara 4: 7–38.
de los valles occidentales del norte de Chile y sur del Deter CA. 2009. Gradients of occlusal wear in hunter–
Perú’ (Fondecyt 1085106; Universidad de Tarapacá, gatherers and agriculturalists. American Journal of Physical
Chile). We are grateful to Raul Rocha for producing Anthropology 138: 247–254.
Finucane BC. 2009. Maize and sociopolitical complexity in
Figures 1 and 2 and to Misty Fields, Alexis Gray and
the Ayacucho valley, Peru. Current Anthropology 50(4):
Nathan Harper for providing comments on earlier 535–545.
versions of the manuscript. We would also like to Focacci G. 1974. Excavaciones en Playa Miller 7. Chungará
thank the journal editor and the anonymous reviewers 3: 23–74.
for providing critical review and insightful comments Focacci G. 1980. Síntesis de la Arqueología del Extremo
that greatly improved the manuscript. Norte de Chile. Chungará 6: 3–23.
Focacci G, Erices S. 1972–73. Excavaciones en Túmulos de
San Miguel de Azapa (Arica‐Chile). Actas del VI Congreso
References de Arqueología Chilena. Universidad de Chile: Santiago;
47–62.
Allison MJ, Focacci G, Arriaza BT, Standen V, Rivera M, Fujita H, Ogura M. 2009. Degree of dental attrition with sex
Lowenstein J. 1984. Chinchorro, momias de preparación and aging among Jamon and Edo people in Japan. Journal
complicada: Métodos de momificación. Chungara 13: of Oral Bioscience 51(3): 165–171.
155–171. Hillson S. 2002. Dental Anthropology, 3rd edn. Cambridge
Arriaza BT. 1994. Tipología de las momias Chinchorros: University Press: Cambridge.
Evolución de las prácticas de momificación. Chungara 26: Kaidonis JA, Richards LC, Townsend GC, Tansley GD.
11–24. 1988. Wear of human enamel: A quantitative in vitro
Arriaza BT. 1995. Chinchorro bioarchaeology: Chronology assessment. Journal of Dental Research 77: 1983–1990.
and mummy seriation. Latin American Antiquity 6: 35–55. Kaifu Y. 1999. Changes in the pattern of tooth wear from
Arriaza BT, Standen V. 2008. Bioarquologia. Historia Biocultural prehistoric to recent period in Japan. American Journal of
de los Antiguos Pobladores del Extremo Norte de Chile. Editorial Physical Anthropology 109: 485–499.
Universitaria: Santiago. Kelley MA, Levesque DR, Weidl E. 1991. Contrasting
Arriaza BT, Doubrava M, Standen V, Haas H. 2005. patterns of dental disease in five early northern Chilean
Differential mortuary treatment among the Andean groups. Advances in Dental Anthropology, MA Kelley, CS
Chinchorro fishers: Social inequalities or in situ regional Larsen (eds.). Wiley‐Liss: New York; 203–213.
cultural evolution? Current Anthropology 46(4): 662–671. Kidder A. 1962. South American high cultures. Prehistoric
Bailey SE. 2004. A morphometric analysis of maxillary molar Man in the New World, JD Jennings, E Norbeck (eds.).
crowns of Middle–Late Pleistocene hominins. Journal of University of Chicago Press: Chicago; 451–488.
Human Evolution 47(3): 183–198. Kidder A, Lumbreras L, Smith DB. 1963. Cultural development
Benfer RA, Edwards DS. 1991. The principle axis method in the central Andes‐Peru and Bolivia. Aboriginal Cultural
for measuring rate and amount of dental attrition: Development in Latin America: Interpretive Review, BJ Meggers,
Estimating juvenile or adult tooth wear from unaged C Evans (eds.). Smithsonian Miscellaneous Collections, Vol.
adult teeth. Advances in Dental Anthropology, MA Kelley, CS 146. Smithsonian Institute: Washington, DC; 89–102.
Larsen (eds.). Wiley‐Liss: New York; 325–340. Kieser JA. 1990. Human Adult Odontometrics. The Study of
Buikstra JE, Ubelaker DH. 1994. Standards for Data Collection Variation in Adult Tooth Size. Cambridge Studies in Biological
from Human Skeletal Remains. Arkansas Archaeological Anthropology Series No. 4. Cambridge University Press:
Survey: Fayetteville. Research Series No. 44. Cambridge.
Chattah NL, Smith P. 2006. Variation in occlusal dental Kieser JS, Dennison KJ, Kaidonis JA, Huang D, Herbison
wear of two Chalcolithic populations in the southern PGP, Tayles NG. 2001. Patterns of dental wear in the
Levant. American Journal of Physical Anthropology 130: early Maori dentition. International Journal of Osteoarchaology
471–479. 11: 206–217.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
Tooth Wear in Northwest Chile 301

Larsen CS. 1981. Skeletal and dental adaptations to the shift Muñoz I. 1981. Investigaciones arqueológicas en los túmulos
to agriculture on the Georgia coast population. Current funerary del valle de Azapa (Arica). Chungara 6: 57–95.
Anthropology 22: 422–423. Muñoz I. 1983. La fase Alto Ramírez en los valles del
Larsen CS. 1997. Bioarchaeology: Interpreting Behavior from the extremo norte de Chile. Documentos de Trabajo 3: 3–42.
Human Skeleton. Cambridge studies in biological anthro- Muñoz I. 1989. El período Formativo en el Norte Grande (1.000
pology. Cambridge University Press: Cambridge. a.C. a 500 d.C.). Culturas de Chile Prehistoria: Desde sus Orígenes
Larsen CS. 2002. Post‐Pleistocene human evolution: hasta los Albores de la Conquista, J Hidalgo, V Schiappacasse,
Bioarcheology of the agricultural transition. Human Diet: H Niemeyer, C Aldunate, I Solimano (eds.). Andrés Bello:
Its Origin and Evolution, PS Ungar, MF Teaford (eds.). Santiago; 107–128.
Bergin and Garvey: Westport; 19–36. Muñoz I. 2004. El periodo Formativo en los Valles del Norte
Littleton J, Frohlich B. 1993. Fish eaters and farmers: Dental de Chile y Sur de Peru: Nuevas Evidencias y Comentarios.
pathology in the Arabian Gulf. American Journal of Physical Chungara (Vol. Especial, 2004): 213–225.
Anthropology 92(4): 427–447. Muñoz I, Chacama J. 1982. Investigaciones arqueológicas
Liu W, Zhang QC, Wu XJ, Zhu H. 2010. Tooth wear and en las poblaciones precerámicas de la costa de Arica.
dental pathology of the Bronze–Iron Age people in Documentos de Trabajo 2: 3–96.
Xinjiang, Northwest China: Implications for their diet Muñoz I, Rocha J, Chacón S. 1991. Camarones 15: Asentamiento de
and lifestyle. HOMO—Journal of Comparative Human Biology pescadores correspondiente a los períodos Arcaico y Formativo. Actas
61(2): 102–116. del XI Congreso de Arqueología Chilena. Tomo II. Museo
Lukacs JR. 1992. Dental paleopathology and agricultural Nacional de Historia Natural: Santiago; 1–24.
intensification in south Asia: New evidence from Bronze Osborn JW. 1984. Helicoidal plane of dental occlusion.
Age Harappa. American Journal of Physical Anthropology 87(1): American Journal of Physical Anthropology 57: 273–281.
133–150. Pearsall DM. 2008. Plant Domestication and the Shift to
Lukacs JR. 1995. The ‘Caries Correction Factor’: a new Agriculture in the Andes. The Handbook of South American
method of calibrating dental caries rates to compensate Archaeology, H Silverman, WH Isbell (eds.). Springer:
for antemortem loss of teeth. International Journal of New York; 105–120.
Osteoarchaeology 5: 151–156. Pechenkina EA, Benfer RA, Zhijun W. 2002. Diet and health
Lukacs JR. 1996. Sex differences in dental caries rates with changes at the end of the Chinese Neolithic: The Yangshao/
the origin of agriculture in south Asia. Current Anthropology Longshan transition in Shaanxi Province. American Journal of
37: 147–153. Physical Anthropology 117: 15–36.
Macchiarelli R. 1989. Prehistoric “fish‐eaters” along the Reinhardt GA. 1983. Attrition and edge‐to‐edge bite. An
eastern Arabian coasts: dental variation, morphology and anthropological study. The Angle Orthodontist 53(2): 157–164.
oral health in the Ra’s al‐Hamra community (Qurum. Rivera MA. 1984. Altiplano and tropical lowland contacts in
Sultanate of Oman, 5th–4th Millennia BC). American northern Chilean prehistory: Chinchorro and Alto Ramírez
Journal of Physical Anthropology 78(4): 575–594. revisited. Social and Economic Organization in the Prehispanic
Mangelsdorf P, Reeves RG. 1939. The origin of Indian corn and Andes, DL Browman, RL Burger, MA Rivera (eds.), vol. 194.
its relatives. Texas Agricultural Station Bulletin 574: 1–315. BAR International Series. Archaeopress: Oxford; 143–160.
Mayhall JT, Kageyama I. 1997. A new, three‐dimensional Rivera MA. 1991. The prehistory of northern Chile: A
method for determining tooth wear. American Journal of synthesis. Journal of World Prehistory 5: 1–47.
Physical Anthropology 103: 463–469. Rivera MA, Soto P, Ulloa L, Kushner D. 1974. Aspectos sobre
Miles AEW. 1963. The dentition in the assessment of individual el desarrollo tecnol6gico en el proceso de agriculturaci6n en
age in skeletal material. Dental Anthropology: Symposia of the el norte prehispanico especialmente Arica (Chile). Chungara
Society for the Study of Human Biology IV, D Brothwell (ed.). 3: 79–107.
Pergamon: New York; 191–209. Rothhammer F, Santoro CM. 2001. El desarrollo cultural en
Miles AEW. 2001. The Miles method of assessing age from el valle de Azapa, extremo norte de Chile y su vinculación
tooth wear revisited. Journal of Archaeological Science 28: con los desplazamientos poblacionales altiplánicos. Latin
973–982. American Antiquity 12: 59–66.
Milner GR, Larsen CS. 1991. Teeth as artifacts of human Rothhammer F, Quevedo S, Cocilovo A, Focacci G, Llop E.
behavior: Intentional mutilation and accidental modifica- 1982. Microevolución en poblaciones prehistóricas del
tion. Advances in Dental Anthropology, MA Kelley, CS Larsen área andina II. Variación craneométrica cronológica en los
(eds.). Wiley‐Liss: New York; 357–378. valles de Arica. Chungara 8: 275–289.
Mølleson T, Jones K, Jones S. 1993. Dietary change and the Rothhammer F, Santoro CM, Moraga M. 2002. Craniofacial
effects of food preparation on microwear patterns in the chronological microdifferentiation of human prehistoric
late Neolithic of Abu Hureyra, northern Syria. Journal of populations of the Azapa Valley, northern Chile. Revista de
Human Evolution 24: 455–468. Chilena Historia Natural 75: 259–264.
Molnar S. 1971. Human tooth wear, tooth function, and Santoro CM. 1980a. Estratigrafía y secuencia cultural funeraria
cultural variability. American Journal of Physical Anthropology fases: Azapa, Alto Ramirez y Tiwanaku (Arica‐Chile).
34: 175–190. Chungara 6: 24–45.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)
302 J. T. Watson et al.

Santoro CM. 1980b. Fase Azapa. Transición del arcaico, al Sutter RC. 2000. Prehistoric genetic and culture change: A
desarrollo agrario inicial en los valles bajos de Arica. bioarchaeological search for pre‐Inka altiplano colonies in
Chungara 6: 46–56. the coastal valleys of Moquegua, Peru, and Azapa, Chile.
Santoro CM. 1980c. Formativo temprano en el extremo Latin American Antiquity 11: 43–70.
norte de Chile. Chungara 8: 33–62. Sutter RC. 2005a. The prehistoric peopling of South America
Sciulli PW. 1997. Dental evolution in prehistoric Native as inferred from epigenetic dental traits. Andean Past 7:
Americans of the Ohio Valley Area. I. Wear and pathology. 183–217.
International Journal of Osteoarchaeology 7: 507–524. Sutter RC. 2005b. A bioarchaeological assessment of
Scott EC. 1979a. Dental wear scoring technique. American prehistoric ethnicity among early Late Intermediate
Journal of Physical Anthropology 51: 213–218. period populations of the Azapa Valley, Chile. Us &
Scott EC. 1979b. Principle axis analysis of dental attrition Them: The Assignation of Ethnicity in the Andean Region:
data. American Journal of Physical Anthropology 51: 203–212. Methodological Approaches, RM Reycraft (ed.). The Cotsen
Scott RG, Winn JR. 2011. Dental chipping: Contrasting Institute of Archaeology, UCLA: Los Angeles; 183–205.
patterns of microtrauma in Inuit and European popula- Sutter RC. 2006. The test of competing models for the
tions. International Journal of Osteoarchaeology, in press. prehistoric peopling of the Azapa Valley, northern Chile,
DOI: 10.1002/oa.1184. using matrix correlations. Chungara 38(1): 63–68.
Smith P. 1972. Diet and attrition in the Natufians. American Sutter RC, Mertz LM. 2004. Non‐metric cranial trait variation
Journal of Physical Anthropology 37: 233–238. and prehistoric biocultural change in the Azapa Valley,
Smith BH. 1984. Patterns of molar wear in hunter–gatherer Chile. American Journal of Physical Anthropology 123: 130–145.
and agriculturalists. American Journal of Physical Anthropology Ubelaker DH. 1978. Human Skeletal Remains: Excavation,
63: 39–56. Analysis, Interpretation. Aldine: Chicago.
Smith BH. 1982. Is there a human pattern of tooth wear? Varela HH, Cocilovo JA. 2002. Genetic drift and gene flow in
American Journal of Physical Anthropology 57: 229. a prehistoric population of the Azapa Valley and coast,
Smith BD. 1998. The Emergence of Agriculture. Scientific Chile. American Journal of Physical Anthropology 118: 259–267.
American Library: New York. Walker PL, Erlandson JM. 1986. Dental evidence for
Stanish C. 2001. The origin of state societies in South prehistoric dietary change on the Northern Channel
America. Annual Review of Anthropology 30: 41–64. Islands, California. American Antiquity 51(2): 357–383.
Steckel RH, Rose JC (eds.). 2002. The Backbone of History: Watson JT. 2008a. Prehistoric dental disease and the dietary
Health and Nutrition in the Western Hemisphere. Cambridge shift from cactus to cultigens in northwest Mexico.
University Press: Cambridge. International Journal of Osteoarchaeology 18(2): 202–212.
Sutter RC. 1997. Dental variation and biocultural affinities among Watson JT. 2008b. Changes in food processing and occlusal
prehistoric populations from the coastal valleys of Moquegua, Peru, dental wear during the Early Agricultural period in northwest
and Azapa, Chile. Unpublished PhD dissertation, Univer- Mexico. American Journal of Physical Anthropology 135: 92–99.
sity of Missouri‐Columbia. Watson JT, Munoz I, Arriaza BT. 2010. Formative
Sutter RC. 1999. The Chinchorros and their ancestors: A adaptations, diet, and oral health in the Azapa Valley,
bioarchaeological assessment of genetic and cultural northwest Chile. Latin American Antiquity 21(4): 423–439.
change in the Azapa Valley, Chile. Journal of the Indiana Yesner DR. 1980. Marine hunter‐gatherers: Ecology and
Academy of Social Sciences III: 77–87. prehistory. Current Anthropology 21(6): 727–750.

Copyright © 2011 John Wiley & Sons, Ltd. Int. J. Osteoarchaeol. 23: 287–302 (2013)

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