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Culture and Ecology of Chaco Canyon and the San Juan Basin

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----------------- -----192 <strong>Chaco</strong> Project Syn<strong>the</strong>sissmaller numbers could have been supported by localagricultural production.Diet <strong>and</strong> HealthFloral <strong>and</strong> faunal remains provide evidence forfoods included in <strong>the</strong> <strong>Chaco</strong>an subsistence base.Analyses <strong>of</strong> coprolites <strong>and</strong> human skeletal remains'provide clues as to how well this diet nourished <strong>the</strong>population. Although samples are limited, someinsights were gained.M. Toll (1985:268) indicated that <strong>the</strong>re are lowlevelshifts in wild plant use through time. As notedpreviously, when <strong>the</strong> ubiquity <strong>of</strong> com is at its lowestlevel at Pueblo Alto during <strong>the</strong> Red Mesa ceramicperiod, <strong>the</strong>re is evidence to suggest widespread use <strong>of</strong>wild plants. There were more species from outside <strong>the</strong>canyon in botanical samples from <strong>Chaco</strong>an greathouses, which might indicate different household <strong>and</strong>subsistence organization (M. Toll 1985:249). Atsmall sites, use <strong>of</strong> firepits vs. heating pits seemed todiffer; <strong>the</strong> former contained more charred economicweeds <strong>and</strong> corncobs, while <strong>the</strong> latter indicated fewfood processing activities. In contrast, at Pueblo Alto<strong>the</strong>se two features seem to have been used in a similarmanner (M. Toll 1985:266). When samples fromsame proveniences were compared, data from pollen<strong>and</strong> flotation samples were <strong>of</strong>ten complementary innature. Data from pollen analysis confirmed <strong>the</strong> use<strong>of</strong> similar domesticated <strong>and</strong> wild plant species at bothlarge <strong>and</strong> small sites (A. Cully 1985b:218), yet <strong>the</strong>distributions <strong>of</strong> com pollen at each <strong>of</strong> <strong>the</strong> sites wasunique. For example, at 29SJ629, <strong>the</strong> pattern couldbe interpreted as perhaps being seasonal in nature.Based on her analysis <strong>of</strong> faunal remains, Akins(1982d, 1984, 1985) indicated major dependence onsmall mammals (e. g., cottontail rabbit, jackrabbit, <strong>and</strong>prairie dog) <strong>and</strong> economic rodents (e.g., squirrel),plus three larger mammals (antelope, deer, <strong>and</strong>pronghorn), over an 800-year period. Yet severaltrends suggested change through time (Akins 1985:389-403). Prairie dog use was always fairly low;prairie dogs tended to show low increased percentagesfrom Red Mesa (A.D. 950 to 1020 or 1040) throughLate Mix (A.D. 1100 to 1150 or 1200). Jackrabbitscontributed more to <strong>the</strong> diet than cottontails during <strong>the</strong>Classic period. The largest number <strong>of</strong> cottontailremains were associated with <strong>the</strong> Red Mesa <strong>and</strong>Gallup (A.D. 1040 to 1100) ceramic assemblages.The peak in jackrabbit remains correlated with <strong>the</strong>Gallup ceramic assemblage, <strong>and</strong> remained high <strong>the</strong>reafter.Around A.D. 920 to 950, <strong>the</strong>re was a shift inartiodactyl remains that suggested less dependence onpronghorn <strong>and</strong> greater dependence on deer. Although<strong>the</strong> number <strong>of</strong> mountain sheep remains fluctuated, noclear pattern could be discerned. Carnivores werepresent in low numbers; <strong>the</strong>ir presence increasedbetween A.D. 850 <strong>and</strong> 1000. Turkeys also appearedin low numbers until very late. The overall pattern atboth small sites <strong>and</strong> great houses suggested that <strong>the</strong>rewas increased use <strong>of</strong> animals with larger body sizebeginning around A.D. 950 <strong>and</strong> continuing throughout<strong>the</strong> Classic period. Akins attempted to quantify <strong>the</strong>possible differences between remains found at <strong>the</strong>small sites vs. great houses, but <strong>the</strong> number <strong>of</strong> assumptionsthat would have had to be made was toogreat. These species that were recovered are typical<strong>of</strong> those found at o<strong>the</strong>r sites in <strong>the</strong> <strong>San</strong> <strong>Juan</strong> <strong>Basin</strong> <strong>and</strong>on <strong>the</strong> Colorado Plateau (Dean et al. 1985).Two early studies <strong>of</strong> coprolites (Bc 288, <strong>the</strong>Gallo Cliff Dwelling, by Callen 1977; Kin Kletso, byConley 1977) suggested that all foods included in <strong>the</strong><strong>Chaco</strong> diet may not appear in coprolites, yet someunintentional materials do accompany meat <strong>and</strong>vegetal selections. Ingestion <strong>of</strong> several plant <strong>and</strong>animal taxa was confirmed by more detailed studies <strong>of</strong>bone (Gillespie 1981), macrobotanical remains (M.Toll 1981), <strong>and</strong> pollen (Clary 1981, 1983a, 1983b,1984) found in coprolites recovered from three sitesexcavated by <strong>the</strong> <strong>Chaco</strong> Project.Based on pollen recovered in coprolites, Clary(1983a, 1983b, 1984) confirmed that <strong>the</strong> diet at <strong>the</strong>great houses (Pueblo Bonito, Pueblo Alto, <strong>and</strong> KinKletso) between about A.D. 1000 <strong>and</strong> 1150 was verysimilar. Among <strong>the</strong> taxa recovered were two cultivars(com [Zea mays] <strong>and</strong> squash [Curcubita sp.]). Beans(Phaseolus sp.), which are difficult to recover because<strong>of</strong> poor preservation <strong>and</strong> limited pollen distribution,were absent in <strong>the</strong>se samples even though <strong>the</strong>y arereported from Bc 288 (Callen 1977). Weedy economicspecies that probably were encouraged to growwere also present. Pollen samples included goosefoot<strong>and</strong> amaranth (Chenopodiacea <strong>and</strong> Amaranthus sp.,including pigweed); mallow (Sphaeralcea sp.); wildsunflower (Helianthus sp.), <strong>and</strong> o<strong>the</strong>r members <strong>of</strong> <strong>the</strong>sunflower family (Compositae); beeweed (Cleome

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