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