deposition in the year
following the closure. However, there was no direct way to ascribe this
reduction to the smelter closure. Below are the measurements of nitrate
and arsenic for this network.

There should be no relation between the smelter closure and nitrate deposition, since the smelter was no source of nitrate. On the other hand, the smelter was by far the leading source of arsenic, and the substantial decrease in the arsenic deposition in southern BC is an indication of long range transport of pollutants from the Tacoma smelter having been a factor in BC air pollution.

Each rain event sampled was pre-selected according to meteorological criteria, specifying winter rains from cyclonic frontal systems with SSW winds, no convergence, and relatively uniform precipitation over the extent of the network. If a morning forecast (based on 950-500 mb weather maps, NOAA's aloft soundings at Quillayute on the Washington coast, satellite imagery, and local weather observations) predicted these conditions, the samplers were deployed at noon. During February and March of 1985 and 1986, 14 events were sampled (7 before and 7 after closure). Of these, 10 events (5 before and 5 after closure) were meteorologically consistent with the forecast criteria, with 24 hr precipitation accumulations of 0.35 to 1.0 cm.
The 38 sampling sites were organized into spatially homogeneous classes
based on the known wind direction and the location of major
SO
emission sources. There were
6 sites upwind of the smelter with hight quality data
(Class 1 in the map above), 8 sites immediately
downwind of the smelter (Class 2), and 11 sites downwind of both the smelter
and South Seattle. Several other sites were east of the smelter and/or
near local point sources (Classes 4 and 5).
STAT 498: Copyright© 1996, Peter Guttorp.
Email corrections or comments to Peter Guttorp.
Last updated October 14, 1998.