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Northeast Subsistence-Settlement Change: A.D. 700 –1300

Northeast Subsistence-Settlement Change: A.D. 700 –1300

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Herbaceous and shrubby vegetation increases at<br />

the camp margins, giving way to general disclimax<br />

forest which provides firewood. Winter<br />

trapping camps are in more protected locations.<br />

[Yarnell 1984:108]<br />

Crawford (1997) used weed seeds as an indicator of<br />

anthropogenesis in prehistoric northeastern Japan. He<br />

pointed out that anthropogenesis is a critical factor in<br />

the success of human cultures. By removing trees<br />

from a habitat, humans set in motion processes that<br />

change the character of the ecosystem, taking the system<br />

back to less mature successional stages. Young<br />

successional stages are characterized by rapid reproductive<br />

rates, short life cycles, and a high ratio of production<br />

to respiration, resulting in greater quantities<br />

of fruit and vegetal materials, as well as greater numbers<br />

of animals, such as deer and rodents (Crawford<br />

1997:87). Crawford identified patterns involving relative<br />

abundance of annual weeds (indicative of regular<br />

short-term disturbance) and perennial weeds (indicative<br />

of early successional stages that would be associated<br />

with forest edge or village edge communities).<br />

Quantitative analysis of archaeological plant<br />

remains makes it possible to draw inferences about<br />

the degree of anthropogenic disturbance of plant<br />

communities in the vicinity of a site through time.<br />

This paper will use a variety of indicators to trace<br />

changes in plant assemblages in the <strong>Northeast</strong> from<br />

the Archaic through the Contact periods. This<br />

approach is essential to understanding the particular<br />

changes in plant communities that are associated with<br />

the adoption of agriculture and may make it possible<br />

to recognize occupations that represent early experimentation<br />

with agriculture, as hypothesized by John<br />

Hart (1999) in his Darwinian perspective on the evolution<br />

of maize agriculture in the Eastern Woodlands.<br />

To recognize evidence of anthropogenesis, it is first<br />

necessary to consider what the undisturbed vegetation<br />

of northeastern sites would have been like and<br />

how it may have differed from south to north.<br />

FOREST REGIONS OF THE NORTHEAST<br />

A comprehensive account of the original forest pattern<br />

of eastern North America was constructed by<br />

Lucy Braun in 1950. According to her model, much of<br />

northern New England and New York State at settlement<br />

was covered with a hemlock–white<br />

pine–northern hardwoods forest (Figure 13.1).<br />

Northward, the shorter growing season and low winter<br />

temperature extremes eliminated one after another<br />

of the deciduous forest species. Maine archaeological<br />

sites fall within the New England section and most<br />

of the New York sites lie within the Allegheny section<br />

of the hemlock–white pine–northern hardwoods forest<br />

(Figure 13.2). In New York, the chestnuts, oaks,<br />

and hickories of the southern forests extended up the<br />

major river valleys into the state (Braun 1950:395).<br />

Many of the New York sites in the present study are<br />

located in the Susquehanna drainage, some in the valleys<br />

and some in the uplands. The Memorial Park site<br />

in the Susquehanna River Valley in Pennsylvania is at<br />

the edge of Braun’s oak–chestnut forest region, which<br />

extends up into southern New England and the<br />

Hudson River Valley in New York. The present study<br />

includes three sites from the oak–chestnut forest<br />

region in Connecticut and adjacent New York State.<br />

Latitudinal differences in the number of tree<br />

species are significant in the case of those with edible<br />

nuts, particularly oaks and hickories. In Maine there<br />

are only three species of nut trees that are widespread—red<br />

oak, beech, and beaked hazelnut—out of<br />

a total of 14 species of nut trees found in the state (see<br />

maps in Asch Sidell 1999d:196). In New York, this<br />

increases to seven widespread species, and in<br />

Pennsylvania, eight (Table 13.1). In southern New<br />

England, there are 15 species of nut trees that are<br />

widespread (Little 1971, 1977).<br />

INDICATOR SPECIES<br />

Keeping in mind that tree species occur in different<br />

combinations in different regions and that the ecological<br />

significance of a species may vary between<br />

regions (Braun 1950:37), the archaeological wood<br />

species can be grouped to form indicators of several<br />

plant communities or habitats. For <strong>Northeast</strong>ern sites,<br />

some communities that can be inferred from archaeological<br />

wood are mesic forest; dry, open woods; disturbed<br />

woods or thickets; and bottomland forest<br />

(Table 13.2).<br />

The first group of species, labeled “mesic forest,” is<br />

indicative of a mature northern hardwoods–hemlock–white<br />

pine forest. Sugar maple,<br />

beech, and hemlock were important components of<br />

that forest (Braun 1950). These species grow in rich<br />

soil, are shade tolerant, and thrive in a closed forest<br />

with moderate moisture. Yellow birch (Betula<br />

alleghaniensis) and sweet birch (B. lenta) are also shade<br />

tolerant and common in rich soil of moist woods and<br />

slopes (House 1924:270). White pine formerly was a<br />

242 Sidell

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