Groundwater plumes containing dissolved uranium at levels above natural bac
kground exist adjacent to uranium ore bodies, at uranium mines, milling loc
ations, and at a number of explosive test facilities. Public health concern
s require that some assessment of the potential for further plume movement
in the future be made. Reaction-transport models, which might conceivably b
e used to predict plume movement, require extensive data inputs that are of
ten uncertain. Many of the site-specific inputs are physical parameters tha
t can vary spatially and with time. Limitations in data availability and ac
curacy means that reaction-transport predictions can rarely provide more th
an order-of-magnitude bounding estimates of contaminant movement in the sub
surface. A more direct means for establishing the limits of contaminant tra
nsport is to examine actual plumes to determine if, collectively, they spre
ad and attenuate in a reasonably consistent and characteristic fashion.
Here a number of U plumes from ore bodies and contaminated sites were criti
cally examined to identify characteristics of U plume movement The magnitud
e of the original contaminant source, the geologic setting, and the hydrolo
gic regime were rarely similar from site to site. Plumes also spanned a vas
t range of ages, and no complete set of time-series plume analyses based on
the spatial extent of U contamination exist for a particular site. Despite
the accumulated uncertainties and variabilities, the plume data set gave a
clear and reasonably consistent picture of U plume behavior. Specifically,
uranium plumes:
. Appear to reach steady-state, that is, they quit spreading, rapidly (with
in a few years).
. Exceed roughly 2 km in length only in special cases (e.g., where in situ
leaching has been carried out). The majority are much smaller.
. Exhibit very similar U chemistry between sites. This implies analogous co
ntaminant attenuation mechanisms despite their location.