2. OVERVIEW OF TRANSPORT AND MIXING PHENOMENA AND
THEIR IMPLICATIONS
2.1 TRANSPORT AND MIXING PHENOMENA
The findings below are drawn from the analyses described in the
following sections. The section(s) which provide support information
are noted in parentheses.
- Transport of ozone and precursors is affected by flow regimes
that differ with altitude. These regimes can be divided into three
general categories plus a subset of the lowest-altitude regime.
(Sections 3-6)
1) Boundary Layer Synoptic Transport 800-2000 m msl ±
- Transport across the Appalachians - from western OTR and Midwest
- Flow from west to northwest during most episodes
- Transport distance of 300-800 km (200-500 miles) in 24 hours
- Does not have strong diurnal component
2) Channeled Flows Below the Ridge Heights 200-800 m msl ±
- Includes low-level jets (occurred on 6 of 9 1995 regional O3
episodes)
- Includes flow modified by the Appalachian lee trough
- Often transports substances from southwest along urban corridor,
but other directions occur, including flow through gaps in the
Appalachians
- Transport distance of 200-400 km (125-250 miles) overnight
3) Near Surface Flows 0-200 m msl ±
- Light winds in night and morning allow accumulation
- Fresh emissions and urban plumes move downwind and react during
daytime
- O3 aloft and aged precursors are entrained as the
mixing layer deepens
- Transport is typically to the north through east along the urban
corridor for 50-250 km (30-150 miles) by evening.
3a) Offshore Flows (subset of 3 above, see Section 6 for
details) 0-200 m msl ±
- Light winds in night and morning allow accumulation onshore
- Accumulated urban emissions can transport offshore and react
during daytime
- Transport is typically to the northeast through east: Boston
to NH, ME; Philadelphia and NJ to Long Island; Baltimore/Washington
across bay to DE
- Transport can be 200 km (125 miles) or more during daytime and
evening
- Layer stays stable and thin over water, with minimal mixing
and no added emissions
- Can cause high concentrations at shoreline; dilutes with mixing
as transported inland
These flow regimes are shown schematically in Figure 2-1.
- The first two flow regimes above became decoupled from the
surface flow and were accelerated on the episode nights studied.
During the day, winds throughout the boundary layer become coupled,
and winds can become similar through all three regimes. During
the day, frictional effects can slow the winds aloft below the
nighttime speeds. On most episode nights studied, a jet occurred
in a layer just above the surface, where the speeds were higher
than those above or below. On some nights, the winds aloft did
not form a jet (i.e., they were not faster than the winds both
above and below). They were, however, faster than the winds below.
This is a normal occurrence on most summer nights. When the frictional
effects are decoupled, the winds aloft will be faster than the
surface winds. When the aloft winds are decoupled from the surface,
ozone and precursors aloft can be transported without deposition
to or input from the surface layer. (Sections 3-5)
- Trajectory analyses and aloft ozone measurements show ozone
can be transported 300-800 km (200-500 miles) across the Appalachians
at higher altitudes (800-2000 m msl) and 200-400 km (125-250 km)
along the corridor or through gaps in the mountains below the
ridge heights (200-800 m msl). (Sections 3-5,
8)
- Transport over distances of 200-800 km (125-800 miles) or
more of ozone and aged precursors can result in urban corridor
background ozone concentrations of 80-100 ppb. The resulting background
ozone is a mixture of ozone transported from different locations
at different altitudes. (Sections 4-6,
8)
- From early morning ozone and NOy measurements aloft,
long-range transport seems to contribute mainly ozone and aged
precursors, but fresh primary NOx emissions also can
be transported overnight in these flows. (Section 8)
- Ozone of 80-100 ppb or more and aged precursors can remain
aloft overnight and be mixed with fresh emissions (or ozone) the
next day. (Sections 8-9)
- Aloft wind measurements show the source of the air aloft can
be very different from the surface air. (Sections 3-6)
- Resulting surface ozone concentrations depend on the same-day
surface emissions as well as ozone mixed down from aloft. (Section 8,
9)
- Ozone aloft can influence surface concentrations through addition
of aloft ozone and precursors to the surface concentrations as
the mixing layer deepens and entrains them. (Section 8,
9)
- Simple two-layer box-model simulations for conditions similar
to August 1, 1995 and with many simplifying assumptions were performed.
Assumed VOC and NOx emissions were varied by a factor
of four to assess sensitivity to emissions, and two different
chemical mechanisms were used. These simulations indicated that
ozone carryover aloft might increase the maximum surface concentrations
downwind of major urban areas by less than one third to over 100
percent of the aloft excess over 40 ppb (clean air) for the range
of emissions used. Most of the simulations were in the bottom
half of this range. On August 1, 1995, ozone carryover aloft was
roughly 70-80 ppb. Given this range for the initial concentration
in the upper box of the model, the maximum ozone values predicted
for the lower box of the model increased by 13 to over 40 ppb
from what they would have been with only 40 ppb of ozone aloft.
This increase would be less if a higher ozone concentration were
assumed for clean air. (Section 9)
- For the range of conditions simulated with the box model,
roughly 60-75 percent of the maximum ozone seen in the lower layer
was due to same day emissions in the lower layer plus natural
background from aloft; while roughly 25-40 percent was due to
carryover and formation in the upper box. However, reducing ozone
concentrations in the upper box generally did not decrease the
concentrations in the lower box in proportion. (Section 9)
- Maps of surface ozone concentrations, aircraft data downwind
of cities, and analyses of offshore transport suggest that same-day
urban plumes can add 75-100 ppb of ozone to observed nonurban
background concentrations. (Section 6)
- Trajectory analyses and aircraft data indicate that same-day
emissions transported offshore near the surface can cause ozone
exceedances at downwind shoreline locations. These exceedances
are not influenced significantly by ozone aloft. (Section 6)
- Mixing heights increased more slowly on widespread episode
days. (Section 7)
- This can result in accumulation of higher precursor concentrations
in the surface layer in the morning through lower mixing heights.
- This will result in higher precursor concentrations in layers
transported offshore in the morning.
2.2 IMPLICATIONS REGARDING SPATIAL
SCALE OF INFLUENCE
The findings summarized in Section 2.1 shed some light on the
spatial scale of influence of ozone and precursors transported
aloft overnight versus ozone formed from precursors emitted on
the episode day. Our interpretation of the above findings leads
to the following conclusions.
- The three-dimensional air quality and wind data show that
aloft transport can result in the widespread occurrence of overnight
ozone carryover aloft at average boundary layer concentrations
of 70-90 ppb. When mixed to the surface, this transport can lead
to surface ozone concentrations of 70-90 ppb. (See Sections 8,
9). This surface background contribution is roughly 30-50 ppb
above clean air, assuming a clean-air value of about 40 ppb. This
background carryover ozone can be caused by emissions or ambient
ozone coming from 200-800 km (125-500 miles) away since the prior
day.
The aircraft data and plots of surface maximum ozone show same-day
plumes (or pulses) of ozone downwind of urban areas embedded in
a regional background. The peak urban plume concentrations were
up to 80-100 ppb higher than the nearby regional upwind or crosswind
concentrations. Offshore transport of near-surface emissions was
seen to cause downwind offshore and shoreline concentrations that
were 80-100 ppb higher than the concentrations higher aloft and
at downwind onshore areas not impacted by the transported plume.
Under these conditions, even with clean air as a background, urban
plumes resulting from same-day emissions could cause ozone concentrations
to exceed federal standards 50-250 km (30-150 miles) downwind.
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