Trajectory analyses shown in Figures 3-6,
3-7, and 3-8
and the vertical wind profiles in Figures 3-1,
5-3, 5-5,
5-7, and 5-9
showed that surface flows were disconnected from the aloft flows
at night and early morning and were generally light, allowing
emissions to accumulate overnight and be transported downwind
during the day. The effects of the accumulated emissions can be
detected downwind as ozone pulses when the ozone formed from the
same-day urban emissions arrives at downwind receptors. In NARSTO-Northeast,
urban plumes or pulses were documented by aircraft flights and
surface measurements downwind of OTR cities and were traced offshore
to downwind onshore receptors.
Figure 6-1, adapted from Zhang et
al. (1996), shows the surface and aloft (500 m msl)
ozone concentrations downwind of OTR urban areas in midafternoon
on July 14. The surface concentrations at the top of the figure
are hourly averages for the hour starting at 1500 EST (1600
EDT). The concentrations in the bottom part of the figure are
instantaneous aircraft measurements during afternoon flights of
two aircraft, one coming from Maine and the other from Virginia,
and both landing in southeastern New York. The aircraft data shown
are for those portions of the flights that were between 400 and
600 m msl. The surface mixing layer was deep enough by the time
of the flights that surface emissions would have been mixed to
the level shown. The aircraft measurements are described by Anderson
et al. (1997).
Figure 6-1 shows ozone concentrations above the federal standards
along the Connecticut shoreline and over Long Island Sound, over
and offshore of central New Jersey, and in northeastern Maryland.
Figure 6-2 shows the near-surface
back trajectories from several receptor sites for the same afternoon.
The trajectories generally come from the southwest and are consistent
with transport since early morning from the New York City, Philadelphia,
and Baltimore-Washington areas, respectively. The downwind ozone
pulses of 150 to over 175 ppb are superimposed on regional background
concentrations of 75-100 ppb throughout most of the OTR. This
implies that the same-day urban emissions added 75-100 ppb
of ozone over the regional background concentrations. Assuming
a clean-air concentration of 40 ppb and assuming the regional
background concentrations were due to transport aloft, the aloft
transport contribution on this day would have been 35-60 ppb.
On August 1, high ozone concentrations were measured along the
coast of Maine. The maximum concentrations, the time of occurrence
of the peaks, and surface back trajectories from the times of
the peaks are shown in Figure 6-3.
The surface back trajectories for this figure were calculated
manually by interpolating the hourly wind data from shoreline
locations and offshore buoys. The trajectories were calculated
manually because the CALMET model was not able to resolve the
lowest-level flows over the ocean. Concentrations as high as 172 ppb
at Phippsburg ME and over 150 ppb at several locations were observed
along the Maine coast, while the highest concentration seen at
an inland Maine site was 102 ppb. The progression of the time
of the maxima from south to north along the coast suggested transport
from the Boston area. The trajectory analyses confirmed this hypothesis.
Surface winds for Boston, Cape Elizabeth, and two buoys are shown
in Figure 6-4. The winds were offshore
from the southwest during the night and morning hours, turning
southerly offshore during the afternoon, and carrying the urban
plume from eastern Massachusetts onshore along the Maine coast.
Offshore, the region of high ozone was confined below 400 m msl,
as seen in Figure 65, which
shows an aircraft spiral made offshore of the southern tip of
Maine. The spiral location is shown in Figure 6-3. The spiral
shows the highest ozone concentration immediately next to the
surface. Above the surface layer were carried-over ozone concentrations
of about 70 ppb between 400 and 900 m and 50 ppb above 1000 m
msl.
An ozone concentration of 166 ppb (comparable to the maximum shoreline
concentrations) was measured offshore of Phippsburg by the Scotia
Prince ferry boat at the location shown in Figure 6-3. The concentrations
measured each hour by the boat are shown in Figure 6-6.
The ferry data show the ozone pulse near the shoreline, but also
show that the pulse had passed the ferry port at Portland by 1900
EST.
Onshore, the highest concentrations in Maine were seen a few hours
after the peak shoreline concentrations and were substantially
lower. This is consistent with continued transport inland and
with dilution of the surface-based ozone by the lower concentrations
seen aloft. The dilution would occur as the surface air was mixed
aloft by heating and turbulence when it crossed the shoreline.
Farther inland, beyond the impact of the onshore flow, the maximum
concentrations occurred earlier in the day and were consistent
with the concentrations that would have occurred if the 50 and
70 ppb carryover values seen aloft in the aircraft spiral had
been mixed to the surface.
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