Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-26T20:01:35.118Z Has data issue: false hasContentIssue false

ACCELERATOR MASS SPECTROMETRY DATING OF MEADOWCROFT ROCKSHELTER MAIZE

Published online by Cambridge University Press:  19 April 2022

John P Hart*
Affiliation:
New York State Museum, 3140 Cultural Education Center, Albany, NY12203, USA
J M Adovasio
Affiliation:
Senator John Heinz History Center, 1212 Smallman St, Pittsburgh, PA15222, USA
*
*Corresponding author. Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

The Meadowcroft Rockshelter in southwestern Pennsylvania is best known for its pre-Clovis occupation. Potentially important for later times is the recovery of maize macrobotanical remains from higher strata dating as early as the 4th century BC based on radiometric radiocarbon (14C) dates on wood charcoal. These remains have been considered to be potentially as old as the earliest microbotanical evidence for maize in Michigan, New York and Québec recovered from directly dated charred cooking residues adhering to pottery. The results of accelerator mass spectrometry (AMS) dating 17 samples from maize specimens from all Meadowcroft strata producing maize, indicate that the specimens originated from historical use of the shelter, most likely after AD 1800. These results further emphasize the need to obtain direct dates on maize macrobotanical remains recovered from early contexts prior to the development and common use of AMS dating.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2022. Published by Cambridge University Press for the Arizona Board of Regents on behalf of the University of Arizona

INTRODUCTION

The histories of the spread of maize (Zea mays ssp. mays) north and south of central Mexico where it evolved from an annual teosinte (Zea mays ssp. parviglumis) 9000–7000 years ago (Matsuoka et al. Reference Matsuoka, Vigouroux, Goodman, Sanchez and Buckler2002), its adaptations to wide ranges of climatic and edaphic conditions, the timings of its adoptions by far-flung Native American societies, and the impacts of its adoption, if any, on regional subsistence-settlement systems remain important topics of research for archaeologists, geneticists, and paleoethnobotanists (e.g., Staller et al. Reference Staller, Tykot and Benz2006; Bonavia Reference Bonavia2013; Grobman Reference Grobman and Bonava2013; Blake Reference Blake2015; Pearsall Reference Pearsall2019). While major strides have been made in the past few decades in building knowledge on each of these topics through a variety of analytical methods and techniques, the crop’s histories remain far from settled in many regions. One such region is temperate northeastern North America (hereafter Northeast), one of the last regions where maize was adopted, but where it became the main crop of agricultural systems after AD 1000–1300 (Hart and Lovis Reference Hart and Lovis2013). Resolving the timing of the crop’s adoption is necessary to anchor maize’s histories in this region and has been a long-standing focus of research that is yet to be resolved (e.g., Emerson et al. Reference Emerson, Hedman, Simon, Fort and Witt2020; Dotzel Reference Dotzel2021; Simon et al. Reference Simon, Hollenbach and Redmond2021; Stewart Reference Stewart2021). Current microbotanical evidence from Michigan (Schultz site; Albert et al. Reference Albert, Kooiman, Clark and Lovis2018), New York (Vinette site; Hart et al. Reference Hart, Brumbach and Lusteck2007a), and Québec (Place-Royale site; Gates St-Piere and Thompson Reference Gates St-Pierre and Thompson2015) (Figure 1), and potentially southern New England (Dotzel Reference Dotzel2021), in the form of phytoliths and starch recovered from accelerator mass spectrometry (AMS)-dated cooking residues adhering to pottery sherd interior surfaces indicates use by at least cal. 300 BC. However, the macrobotanical evidence, which until recently was largely in line with this date for the greater Northeast, is in a state of flux.

Figure 1 Locations of sites mentioned in the text. Circles with dots are sites with recently discredited evidence.

Early applications of accelerator mass spectrometry (AMS) to directly radiocarbon (14C) date macrobotanical remains in the Northeast showed that maize recovered from early contexts at several sites dated much later than the contexts suggested (e.g., Conard et al. Reference Conard, Asch, Asch, Elmore and Gove1984; Murphy Reference Murphy1989). On the other hand, AMS dates on material identified as maize from several sites seemingly confirmed an early presence for the crop (Figure 1). Two sites in particular produced dates that have anchored macrobotanical evidence for early maize (Smith Reference Smith, Boivin, Petraglia and Crassard2017): Holding in Illinois (2077 ± 70 BP, cal 2σ 355 BC–AD 116, median 90 BC; 2017 ± 50 BP, cal 2σ 93 BC−AD 69, median 9 BC; Riley et al. Reference Riley, Walz, Bareis, Fortier and Parker1994) and Edwin Harness Mound in Ohio (1730 ± 60 BP, cal 2σ AD 136–423, median AD 303; Ford Reference Ford1987) along with Icehouse Bottom to the south in Tennessee (1730 ± 85 BP, cal 2σ AD 129–537, median AD 329 and 1720 ± 105 BP, cal 2σ AD 84−569, median AD 338; Chapman and Crites Reference Chapman and Crites1987) (Figure 1). Unlike current practice, the samples used to generate these dates were not subjected to stable carbon isotope ratio measurement. Rather, a mean δ13C value (13C/12C ratio) for C4-pathway plants was used in the 14C age calculations to account for carbon isotope fractionation effects (Taylor and Bar-Yosef Reference Taylor and Bar-Yosef2014). Archaeological maize in the Northeast produces δ13C values (∼ –15.1 to –7.4‰) that are substantially less negative than those of C3-pathway plants (∼ –28.6 to –23.3‰) (Hart et al. Reference Hart, Lovis, Schulenberg and Urquhart2007b). There are C4-pathway plants native to the Northeast such as purslane (Portulaca oleracea, Tankersley et al. Reference Tankersley, Conover and Lentz2016). However, the large structures of maize (kernels, cob fragments) make it unlikely that macrobotanical remains from C4-pathways plants native to the region it would be mistaken for maize. While today δ13C values for fractionation calculations are generally obtained online in the accelerator mass spectrometer on prepared graphite, δ13C values obtained through isotope-ratio mass spectrometry (IRMS) can be used to confirm identifications of maize macrobotanical remains when those identifications are not confident (e.g., Simon et al. Reference Simon, Hollenbach and Redmond2021).

Recently, Simon (Reference Simon2017) obtained δ13C measurements on the originally dated Holding site samples, which indicated they were C3-pathway plant remains rather than maize. Subsequently Simon and colleagues (Reference Simon, Hollenbach and Redmond2021) obtained AMS dates and δ13C measurements on macrobotanical remains identified as maize from Edwin Harness Mound and Icehouse Bottom—the originally dated samples were no longer extant. They found that some remains are not maize based on δ13C values, while others were confirmed as maize but dated much later in time than the original samples. While these results did not prove the originally dated samples were not maize, they did raise that possibility. At present, then, the earliest, as-yet unquestioned, directly AMS-dated macrobotanical sample identified as maize in the Northeast is from the Grand Banks site in southern Ontario (1570 ± 90 BP, cal 2σ AD 258−650, median AD 491; Crawford et al. Reference Crawford, Smith and Bowyer1997) (Figure 1). There is now a chronological gap between the micro- and macrobotanical evidence for maize of over 800 years.

Maize macrobotanical remains potentially older than those from Grand Banks have been recovered from various sites in the Northeast but have yet to be directly dated and subjected to IRMS (McConaughy Reference McConaughy and Hart2008; Hart and Lovis Reference Hart and Lovis2013; Stewart Reference Stewart2021). Obtaining direct dates on these remains coupled with IRMS δ13C measurements to confirm identifications is needed to help clarify the histories of maize in the region.

Caves and rockshelters, two categories of archaeological site relatively rare in the Northeast, provide excellent conditions for preservation of charred and desiccated maize macrobotanical remains and have provided key evidence for early maize in Mexico, Mesoamerica, and the American Southwest (e.g., Piperno and Flannery Reference Piperno and Flannery2001; Merrill et al. Reference Merrill, Hard, Mabry, Fritz and Adams2009; da Fonseca et al. Reference da Fonseca, Smith, Wales, Cappellini and Skoglund2015; Kennett et al. Reference Kennett, Thakar, VanDerwarker, Webster and Culleton2017; Swarts et al. Reference Swarts, Gutaker, Benz, Blake, Bukowski and Holland2017; Torres-Rodríguez Reference Torres-Rodríguez, Vallebueno-Estrada, González, Cook and Montiel2018). Most prominent of such sites in the Northeast is the stratified Meadowcroft Rockshelter located on Cross Creek, an east-west-flowing tributary of the Ohio River, southwest of Pittsburgh, Pennsylvania near the West Virginia boarder (Figure 1; Adovasio et al. Reference Adovasio, Gunn, Donahue and Stuckenrath1978; Adovasio Reference Adovasio2010). Excavated primarily in 1973–1979 and sporadically thereafter, the site is best known for its pre-Clovis component (e.g., Haynes Reference Haynes2015; Carr Reference Carr, Wholey and Nash2018; Williams and Madson Reference Williams and Madsen2020). However, potentially important for maize history is a series of charred and desiccated cobs and cob fragments recovered from later strata as reported in Adovasio and Johnson (Reference Adovasio and Johnson1981). These strata were defined chronologically with radiometric 14C dates on wood charcoal, and as was common practice at the time, these were used to assign dates to the maize (Table 1). 14C dates with median calibrated dates of 403 BC and 349 BC from the earliest stratum to yield maize (Stratum IV) are in-line with the earliest dates for maize microbotanical remains in the Northeast. These finds have been cited as potential evidence for early maize in the Northeast, but the need for direct dates to confirm their early age has been noted often (e.g., Crawford et al. Reference Crawford, Saunders, Smith, Staller, Tykot and Benz2006; McConaughy Reference McConaughy and Hart2008; Hart and Lovis Reference Hart and Lovis2013); it is now accepted practice to directly AMS date crop remains because there is no necessary chronological relationship between spatially associated wood charcoal and the crop remains (Blake Reference Blake, Staller, Tykot and Benz2006). Here, we report direct AMS dates on a series of 17 samples of maize cobs/cob fragments recovered from Meadowcroft. The results emphasize the need to directly AMS date macrobotanical remains of maize and other crops recovered and reported prior to the development and common use of AMS dating.

Table 1 Maize cob data. Associated radiocarbon dates from Adovasio and Johnson (Reference Adovasio and Johnson1981). Rows, grain thickness, cupule width, charring, and notes from Cutler and Blake (Reference Cutler and Blake1977) as published in Adovasio and Johnson (Reference Adovasio and Johnson1981).

* Cutler and Blake (Reference Cutler and Blake1977) indicated this cob fragment was carbonized. However, only two of the samples from this provenience in the collection are carbonized and this fragment is not. The cupule width matches Cutler and Blake’s measurement as well as their statement on glumes.

THE MEADOWCROFT MAIZE REMAINS

Adovasio and Johnson (Reference Adovasio and Johnson1981) reported maize macrobotanical remains in the form of charred and desiccated cobs and cob fragments from the upper strata (IV–XI) of the Meadowcroft Rockshelter (Table 1). Identification of the maize was done by Cutler and Blake (Reference Cutler and Blake1977) at the Missouri Botanical Garden as reported in an unpublished manuscript and summarized by Adovasio and Johnson (Reference Adovasio and Johnson1981). The earliest of these was a small, charred cob fragment identified as probably 16-row popcorn, from Stratum IV associated with 14C dates on wood charcoal of 2355 ± 75 BP and 2290 ± 90 BP. Stratum VI yielded 10-, 12-, and 14-row cob fragments associated with wood charcoal dates of 2155 ± 65 BP and 2075 ± 125 BP. Cob fragments representing 10- and 12-row maize were recovered from Stratum VII with associated wood charcoal dates of 1290 ± 60 BP and 925 ± 65 BP. Botanical remains from Stratum IX included 12- and 14-row maize associated with a date on wood charcoal of 685 ± 80 BP. Cobs and cob fragments from Stratum XI, from 8-, 12-, and 14-rowed maize were reported as dating later than 685 ± 80 BP and earlier than 175 ± 50 BP. In their unpublished report on the maize, Cutler and Blake (Reference Cutler and Blake1977: 1) related that the maize from Meadowcroft was “surprisingly large and vigorous, the cobs firm and thickened.” They indicated that three of the cobs/cob fragments, one from Stratum IX and two from Stratum XI, were possibly modern, post-1800, and recent, respectively (Table 1). This suggested the possibility of some mixing of earlier and later deposits within these strata. They attributed most of the remaining cob fragments in these strata to their prehistoric Midwest 12-Row maize category, with a few ascribed to the prehistoric Eastern 8-Row category.

METHODS AND MATERIALS

The Meadowcroft Rockshelter maize remains are curated at the Senator John Heinz History Center in Pittsburgh along with the rest of the site’s collection. All maize remains are identified by catalog number, wrapped in aluminum foil, and stored in capped plastic vials. The specimens were placed on loan to the New York State Museum (NYSM) where photography and sampling were completed. For catalog numbers with fragments from multiple cobs, cupule width measurements were used to correlate them with Cutler and Blake’s inventory (Table 1). Images and data for the sampled specimens are presented in Supplement 1.

Small samples of 18 cobs and cob fragments were taken under low magnification with a solvent-cleaned scalpel or razor blade. Samples from fragments of different cobs that had been assigned the same Meadowcroft catalog number were given sample numbers to distinguish them in Tables 1 and 2 and Supplement 1. Any adhering sediment was scraped off the area sampled prior to cutting. The samples were weighed, wrapped in aluminum foil, placed in labeled plastic bags, and shipped to the W. M. Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory (KCCAMS) at the University of California-Irvine for isotope-ratio measurement and AMS dating. At KCCAMS, all samples were subjected to the standard acid-base-acid (1N HCl and 1N NaOH, 75°C) pretreatment. Details on sample pretreatment, combustion, graphite reduction, and AMS analysis are available on the KCCAMS website (https://sites.uci.edu/keckams/facilities/). Corrections for isotopic fractionation were performed with δ13C values obtained on prepared graphite using the AMS spectrometer. A Thermo Finnigan Delta Plus stable isotope-ratio mass spectrometer (IRMS) with Gas Bench input was used at KCCAMS to measure δ13C values to a precision of <0.1‰ relative to standards traceable to PDB. The 14C ages were calibrated in OxCal v. 4.4.4 (Bronk Ramsey Reference Bronk Ramsey2009) using the IntCal20 Northern Hemisphere terrestrial 14C calibration curve (Reimer et al. Reference Reimer, Austin, Bard, Bayliss and Blackwell2020).

Table 2 Meadowcroft maize cob samples AMS dating results. Asterisks in the δ13C (‰) column indicate the samples were too small to provide additional material for IRMS measurement.

RESULTS

AMS 14C ages and calibrated dates and δ13C values are presented in Table 2. The sample from specimen FS-1811.1 did not yield enough carbon after pretreatment for analysis, and samples FS-269.8 (2) and FS-130.10 (1) were too small to provide enough material for IRMS measurement. Given the results of the remaining samples, providing additional material of these specimens for assay was unwarranted. While there is no doubt based on Cutler and Blake’s analysis and their physical appearance that the specimens are maize cobs/cob fragments (Supplement 1), the δ13C values ranging from –8.4 to –10.8 confirm their identifications as maize (Table 2).

All dates are historical and remarkably consistent given that the samples were recovered from four separate strata. There is no record and no visual evidence of the maize remains being treated with consolidants or adhesives. The application of most of the commonly used consolidants and adhesives would result in older, not younger, ages than anticipated (Crann and Grant Reference Crann and Grant2019). Three of the organic consolidants and glues analyzed by Crann and Grant (rabbit skin glue, technical gelatine, and wheat starch) produced modern ages.

The technical gelatine analyzed by Crann and Grant was manufactured in 1980, close in time to the Cutler and Blake’s analysis. Using a fraction modern carbon (FMC) value for Meadowcroft specimen FS-811.3 (1) of 0.9875, the FMC of 0.752 for an expected 14C age of 2290 BP, and the FMC value for technical gelatine of 1.103 with the mass balance equation (0.9875–0.752)/(1.1013–0.752)*100 indicates that 67.42% of the 14C in the specimen would need to have been contributed by the technical gelatine to result in an offset of 2190 14C years. This suggests a heavy application that would be visible and prevent the smears of carbon that occurred when handling of the cob fragment for sampling. All consolidants and adhesives tested by Cran and Grant (Reference Crann and Grant2019:1062) have δ13C values more negative than archaeological maize in the Northeast ranging from –36.0 to –15.8‰ (median = –27.5). That the Meadowcroft maize δ13C values are well within the range for archaeological maize in the Northeast also suggests the absence of treatment with consolidants or adhesives. Furthermore, if any of the organic materials analyzed by Crann and Grant had been applied to the Meadowcroft maize specimens, they would have been removed by the base step of the standard acid-base-acid treatment applied to the samples at KCCAMS and have no effect on the analytical results.

The AMS dates, disprove an early presence for maize at the Meadowcroft Rockshelter and go beyond Cutler’s and Blake’s (Reference Cutler and Blake1977) suggestion that three of the specimens date after AD 1800. The calibrated dates are multimodal; the largest probabilities fall within the nineteenth to early twentieth centuries, with probabilities generally <30% falling in the late seventeenth to early eighteenth centuries. When modeled as an OxCal uniform Phase, the 95.4% Date estimate is 1717–1743 (9.3%), 1828–1960 (86.2%). The OxCal runfile for the model is provided in Supplement 2 and full results of the model are presented in Supplement 3. Clearly originating from historical use of the site, the maize remains have no relationship to the long history of Native American occupations of Meadowcroft. Their presence in strata associated with occupations dating as early as the 4th century BC is evidently the result of bioturbation or other disturbance. It should be noted that extreme care was taken during the multiyear excavations at Meadowcroft Rockshelter to note the presence of bioturbation or other disturbances; however, it is apparent that disturbances in the area which produced the maize remains were missed. It should also be stressed that the same strata which yielded the maize remains evidenced no disturbance elsewhere on the site.

DISCUSSION AND CONCLUSIONS

The timings of the adoption of maize are ongoing research topics throughout the Western Hemisphere. In the northeastern North America, two lines of evidence have been used to determine when maize becomes archaeologically visible: microbotanical remains recovered from directly dated food residues adhering to pottery and directly dated macrobotanical remains. Until recently these two lines of evidence were generally in agreement for the region as a whole with early directly dated microbotanical evidence in the eastern Great Lakes and St. Lawrence River Valley and early directly dated macrobotanical evidence from the riverine interior. The early evidence from the riverine interior was recently discredited, leaving the earliest directly dated macrobotanical evidence from the Great Lakes region in southern Ontario, some 800 years later than the earliest directly dated microbotanical evidence. The Meadowcroft maize had the potential to bridge that gap, but it joins a growing list of macrobotanical remains once thought to represent early use of maize in the Northeast that have been shown to date much later in time or to have been misidentified as maize (e.g., Murphy Reference Murphy1989: 348; Conard et al. Reference Conard, Asch, Asch, Elmore and Gove1984; Simon Reference Simon, Raviele and Lovis2014, Reference Simon2017; Simon et al. Reference Simon, Hollenbach and Redmond2021).

At the time the specimens were recovered, the extent of potential biological disturbance was underestimated. Apparently, the maize specimens were transported downward from a higher level and the extent of the bioturbation was not perceived by the excavators. There were no reasons at the time of the Meadowcroft maize recovery to doubt the maize remains’ stratigraphic sequence, association with 14C dates, or Cutler and Blake’s assignments of the majority of cobs to their prehistoric morphotypes. The Meadowcroft results further emphasize the need for AMS dates and δ13C IRMS measures on purported maize macrobotanical remains recovered from contexts in the Northeast that are potentially earlier than Grand Banks such as those listed in Table 3.

Table 3 Examples of potentially early maize macrobotanical remains in the Northeast based on radiocarbon dates on wood charcoal.

The gap between the earliest direct dates on maize micro-and macrobotanical remains in the Northeast continues. This situation is not untypical; maize microbotanical remains pre-date macrobotanical remains in several areas of the Americas where environmental conditions do not favor macrobotanical preservation (e.g., Pohl et al. Reference Pohl, Piperno, Pope and Jones2007; Lombardo et al. Reference Lombardo, Iriarte, Hilbert, Ruiz-Pérez and Capriles2020). Ultimately the two lines of evidence need to be reconciled as suggested by Dotzel (Reference Dotzel2021). This will require additional laboratory and actualistic experimentation to determine under what conditions and contexts maize micro- (Crowther Reference Crowther2012; Raviele Reference Raviele2011) and macrobotanical (e.g., King Reference King1987; Dezendorf Reference Dezendorf2013; Whyte Reference Whyte2019) remains preserve in the archaeological record.

ACKNOWLEDGMENTS

We thank David R. Scofield and the Senator John Heinz History Center for granting access to and allowing analysis of the Meadowcroft Rockshelter maize. We thank John Southon for advice and discussions and Susan Winchell-Sweeney for Figure 1. The AMS dates were funded by the New York State Museum.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/RDC.2022.18

References

REFERENCES

Adovasio, JM. 2010. Moments in time: differential site use patterns at Meadowcroft Rockshelter (36WH297). North American Archaeologist 31:287303.CrossRefGoogle Scholar
Adovasio, JM, Gunn, JD, Donahue, J, Stuckenrath, R. 1978. Meadowcroft Rockshelter, 1977: an overview. American Antiquity 43:632651.CrossRefGoogle Scholar
Adovasio, JM, Johnson, WC. 1981. The appearance of cultigens in the Upper Ohio valley: a view from Meadowcroft Rockshelter. Pennsylvania Archaeologist 51(1–2):6380.Google Scholar
Albert, RK, Kooiman, SM, Clark, CA, Lovis, WA. 2018. Earliest microbotanical evidence for maize in the northern Lake Michigan basin. American Antiquity 83:345355.CrossRefGoogle Scholar
Blake, M. 2006. Dating the initial spread of Zea mays . In: Staller, JE, Tykot, RH, Benz, BF. (eds.), Histories of maize: multidisciplinary approaches to the prehistory, biogeography, domestication, and evolution of maize. Burlington (MA): Academic Press. pp. 4562 Google Scholar
Blake, M. 2015. Maize for the gods: unearthing the 9,000-year history of corn. Oakland: University of California Press.CrossRefGoogle Scholar
Bonavia, D. 2013. Maize: origin, domestication, and its role in the development of culture. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Bronk Ramsey, C. 2009. Bayesian analysis of radiocarbon dates. Radiocarbon 51:337360.CrossRefGoogle Scholar
Carr, KW. 2018. Peopling of the Middle Atlantic. In: Wholey, HA, Nash, CL, editors. Middle Atlantic prehistory: foundations and practice. Lanham (MD): Rowman & Littlefield. p. 219260.Google Scholar
Chapman, J, Crites, GD. 1987. Evidence for early maize (Zea mays) from the Icehouse Bottom site, Tennessee. American Antiquity 52:352354.CrossRefGoogle Scholar
Conard, N, Asch, DL, Asch, MB, Elmore, D, Gove, H, et al. 1984. Accelerator radiocarbon dating of evidence for prehistoric horticulture in Illinois. Nature 308:443446.CrossRefGoogle Scholar
Crann, CA, Grant, T. 2019. Radiocarbon age of consolidants and adhesives used in archaeological conservation. Journal of Archaeological Science: Reports 24:10591063.Google Scholar
Crawford, GW, Saunders, D, Smith, DG. 2006. Pre-contact maize from Ontario, Canada: context, chronology, variation, and plant association. In: Staller, JE, Tykot, RH, Benz, BF, editors. Histories of maize: multidisciplinary approaches to the prehistory, linguistics, biogeography, domestication, and evolution of maize. Burlington (MA): Academic Press. p. 549559.Google Scholar
Crawford, GW, Smith, DG, Bowyer, VE. 1997. Dating the entry of corn (Zea mays) into the lower Great Lakes region. American Antiquity 62:112119.CrossRefGoogle Scholar
Crowther, A. 2012. The differential survival of native starch during cooking and implications for archaeological analyses: a review. Archaeological and Anthropological Sciences 4: 221235.CrossRefGoogle Scholar
Cutler, HC, Blake, LW. 1977. Corn and squash from Meadowcroft Rockshelter. Unpublished report on file at the Senator John Heinz History Center, Pittsburgh, Pennsylvania.Google Scholar
da Fonseca, RR, Smith, BD, Wales, N, Cappellini, E, Skoglund, P, et al. 2015. The origin and evolution of maize in the southwestern United States. Nature Plants 1:15.Google ScholarPubMed
Dezendorf, C. 2013. The effects of food processing on the archaeological visibility of maize: an experimental study of carbonization of lime-treated maize kernels. Ethnobiology Letters 4:1220.CrossRefGoogle Scholar
Dotzel, KM. 2021. Mind the gap: maize phytoliths, macroremains, and processing strategies in southern New England 2500–500 BP. Economic Botany 75:3047.CrossRefGoogle Scholar
Emerson, TE, Hedman, KM, Simon, ML, Fort, MA, Witt, KE. 2020. Isotopic confirmation of the timing and intensity of maize consumption in greater Cahokia. American Antiquity 85:241262.CrossRefGoogle Scholar
Ford, RI. 1987. Dating early maize in the eastern United States. Paper presented at the 153rd American Association for the Advancement of Science Annual Meeting, Chicago, Illinois.Google Scholar
Gates St-Pierre, C, Thompson, RG. 2015. Phytolith evidence for the early presence of maize in southern Quebec. American Antiquity 80:408415.CrossRefGoogle Scholar
Grobman, A. 2013. Appendix: origin, domestication, and evolution of maize: new perspectives from cytogenetic, genetic, and biomolecular research complementing archaeological findings. In: Bonava, D, editor. Maize: origin, domestication, and its role in the development of culture. Cambridge: Cambridge University Press. p. 329486.CrossRefGoogle Scholar
Hart, JP, Brumbach, HJ, Lusteck, R. 2007a. Extending the phytolith evidence for early maize (Zea mays ssp. mays) and squash (Cucurbita sp.) in central New York. American Antiquity 72:563583.CrossRefGoogle Scholar
Hart, JP, Lovis, WA. 2013. Reevaluating what we know about the histories of maize in northeastern North America: a review of current evidence. Journal of Archaeological Research 21:175216.CrossRefGoogle Scholar
Hart, JP, Lovis, WA, Schulenberg, JK, Urquhart, GR. 2007b. Paleodietary implications from stable carbon isotope analysis of experimental cooking residues. Journal of Archaeological Science 34:804813.CrossRefGoogle Scholar
Haynes, G. 2015. The millennium before Clovis. PaleoAmerica 1:134162.CrossRefGoogle Scholar
Kennett, DJ, Thakar, HB, VanDerwarker, AM, Webster, DL, Culleton, BJ, et al. 2017. High-precision chronology for central American maize diversification from El Gigante Rockshelter, Honduras. Proceedings of the National Academy of Sciences 114:90269031.CrossRefGoogle ScholarPubMed
King, FB. 1987. Prehistoric maize in eastern North America: an evolutionary evaluation [Ph.D. dissertation]. University of Illinois at Urbana-Champaign.Google Scholar
Lombardo, U, Iriarte, J, Hilbert, L, Ruiz-Pérez, J, Capriles, JM, et al. 2020. Early Holocene crop cultivation and landscape modification in Amazonia. Nature 581:190193.CrossRefGoogle ScholarPubMed
McConaughy, MA. 2008. Current issues in paleoethnobotanical research from Pennsylvania and vicinity. In: Hart, JP: editor. Current northeast paleoethnobotany II. New York State Museum Bulletin 512. Albany: The University of the State of New York, The State Education Department, Albany. p. 927.Google Scholar
Matsuoka, Y, Vigouroux, Y, Goodman, MM, Sanchez, J, Buckler, E, et al. 2002. A single domestication for maize shown by multilocus microsatellite genotyping. Proceedings of the National Academy of Sciences 99: 60806084.CrossRefGoogle ScholarPubMed
Merrill, WL, Hard, RJ, Mabry, JB, Fritz, GJ, Adams, KR, et al. 2009. The diffusion of maize to the southwestern United States and its impact. Proceedings of the National Academy of Sciences 106:2101921026.CrossRefGoogle Scholar
Murphy, JL. 1989. Archaeological history of the Hocking valley. Athens: Ohio University Press.Google Scholar
Pearsall, DM. 2019. Case studies in paleoethnobotany: understanding ancient lifeways through the study of phytoliths, starch, macroremains, and pollen. New York: Routlege.Google Scholar
Piperno, DR, Flannery, KV. 2001. The earliest archaeological maize (Zea mays L.) from highland Mexico: new accelerator mass spectrometry dates and their implications. Proceedings of the National Academy of Sciences 98:21012103.CrossRefGoogle ScholarPubMed
Pohl, ME, Piperno, DR, Pope, KO, Jones, JG. 2007. Microfossil evidence for pre-Columbian maize dispersals in the neotropics from San Andres, Tabasco, Mexico. Proceedings of the National Academy of Sciences 104:68706875.CrossRefGoogle Scholar
Raviele, ME. 2011. Assessing carbonized archaeological cooking residues: evaluation of maize phytolith taphonomy and density through experimental residue analysis. Journal of Archaeological Science 38:27082713.CrossRefGoogle Scholar
Reimer, PJ, Austin, WEN, Bard, E, Bayliss, A, Blackwell, PG, et al. 2020. The IntCal20 Northern Hemisphere radiocarbon age calibration curve (0–55 cal kBP). Radiocarbon 62:725757.CrossRefGoogle Scholar
Riley, TJ, Walz, GR, Bareis, CJ, Fortier, AC, Parker, KE. 1994. Accelerator mass spectrometry (AMS) dates confirm early Zea mays in the Mississippi River Valley. American Antiquity 59:490498.CrossRefGoogle Scholar
Simon, ML. 2014. Reevaluating the introduction of maize into the American Bottom and western Illinois. In: Raviele, ME, Lovis, WA, editors. Reassessing the timing, rate, and adoption trajectories of domesticate use in the Midwest and Great Lakes. Occasional Papers No. 1. Champaign (IL): Midwest Archaeological Conference, Inc. p. 97134.Google Scholar
Simon, ML. 2017. Reevaluating the evidence for Middle Woodland maize from the Holding site. American Antiquity 82:140150.CrossRefGoogle Scholar
Simon, ML, Hollenbach, KD, Redmond, BG. 2021. New dates and carbon isotope assays of purported Middle Woodland maize from the Icehouse Bottom and Edwin Harness sites. American Antiquity 86:613624.CrossRefGoogle Scholar
Smith, BD. 2017. Tracing the initial diffusion of maize in North America. In: Boivin, N, Petraglia, MD, Crassard, R, editors. Human dispersal and species movement. Cambridge: Cambridge University Press. p. 332348.CrossRefGoogle Scholar
Staller, JE, Tykot, RH, Benz, BF, editors. 2006. Histories of maize: multidisciplinary approaches to the prehistory, linguistics, biogeography, domestication, and evolution of maize. Burlington (MA): Academic Press.Google Scholar
Stewart, RM. 2021. The “Three Sisters” in the upper Delaware valley: implications for the interpretation of local and regional Native American (pre)history. Journal of Middle Atlantic Archaeology 37:134.Google Scholar
Swarts, K, Gutaker, RM, Benz, B, Blake, M, Bukowski, R, Holland, J, et al. 2017. Genomic estimation of complex traits reveals ancient maize adaptation to temperate North America. Science 357:512515.CrossRefGoogle ScholarPubMed
Tankersley, KB, Conover, DG, Lentz, DL. 2016. Stable carbon isotope values (δ13C) of purslane (Portulaca oleracea) and their archaeological significance. Journal of Archaeological Science: Reports 7:189194.Google Scholar
Taylor, RE, Bar-Yosef, O. 2014 Radiocarbon dating: an archaeological perspective. Walnut Creek (CA): Left Coast Press.Google Scholar
Torres-Rodríguez, E, Vallebueno-Estrada, M, González, JM, Cook, AG, Montiel, R, et al. 2018. AMS dates of new maize specimens found in rock shelters of the Tehuacán Valley. Radiocarbon 60:975987.CrossRefGoogle Scholar
Whyte, TR. 2019. An experimental study of bean and maize burning to interpret evidence from Stillhouse Hollow Cave in western North Carolina. Southeastern Archaeology 38:230239.CrossRefGoogle Scholar
Williams, TJ, Madsen, DB. 2020. The upper Paleolithic of the Americas. PaleoAmerica 6:422.CrossRefGoogle Scholar
Wymer, DA. 1992. Trends and disparities: the Woodland paleoethnobotanical record of the Mid-Ohio Valley. In: Seeman, M, editor. Cultural variability in context: Woodland settlements of the Mid-Ohio valley, Special Paper 7, Midcontinental Journal of Archaeology, Kent (OH): Kent State University Press. p. 6576.Google Scholar
Figure 0

Figure 1 Locations of sites mentioned in the text. Circles with dots are sites with recently discredited evidence.

Figure 1

Table 1 Maize cob data. Associated radiocarbon dates from Adovasio and Johnson (1981). Rows, grain thickness, cupule width, charring, and notes from Cutler and Blake (1977) as published in Adovasio and Johnson (1981).

Figure 2

Table 2 Meadowcroft maize cob samples AMS dating results. Asterisks in the δ13C (‰) column indicate the samples were too small to provide additional material for IRMS measurement.

Figure 3

Table 3 Examples of potentially early maize macrobotanical remains in the Northeast based on radiocarbon dates on wood charcoal.

Supplementary material: PDF

Hart and Adovasio supplementary material

Hart and Adovasio supplementary material

Download Hart and Adovasio supplementary material(PDF)
PDF 14.8 MB