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EPA/FLM Single Source LRT Demonstration Project
Bret A. AndersonUSDA Forest Service
10th Conference on Air Quality Modeling10 Conference on Air Quality ModelingEPA‐Research Triangle Park, NC Campus
March 13‐15, 2012
OutlineOutline
• Discuss use of models for AQ/AQRV underDiscuss use of models for AQ/AQRV under NEPA
• Discuss design elements of the EPA/FLM singleDiscuss design elements of the EPA/FLM single source model evaluation project
• Examine initial results of the evaluationExamine initial results of the evaluation project
• Discuss practical considerations of use ofDiscuss practical considerations of use of Eulerian models more routinely in a regulatory framework
NEPA Requirements and the FLM’sNEPA Requirements and the FLM s
• Air quality modeling for NEPA was well definedqua ty ode g o as e de ed– AERMOD for near‐field analyses– CALPUFF for far‐field
• …And then our monitors started to find problems– Winter ozone in Upper Green River Basin in Wyoming
d hand Uinta Basin in Utah
• We now had to address ozone air quality modeling for pollutants that occurred in times ofmodeling for pollutants that occurred in times of the year and in remote locations that were once considered only urban, summertime issues. y ,
The Experience of the Multi‐Use Land Management Agencies
• Multiple use land management agencies such as the Bureau of Land Management (BLM) and US Forest Service (USFS) are responsible for developing environmental impact statements (EIS’) for any resource management d i i th t d f f d l l ddecisions that are made for federal lands.
• For air quality, this means we must analyze potential impacts to local both local and regional air quality for each
t ti th t i id d Thiresource management option that is considered. This translated into running:– AERMOD for near‐field NAAQS/increment analysis
CALPUFF f f fi ld NAAQS/i d AQRV– CALPUFF for far field NAAQS/increment and AQRV– CAMx/CMAQ for ozone NAAQS
The FLM Experience (continued)• The complexity and the cost associated with meeting the needs of air quality
analyses under NEPA have grown considerably in the last five years.
• In response USDA DOI and USEPA entered into a memorandum of understandingIn response, USDA, DOI, and USEPA entered into a memorandum of understanding outlining generally agreed upon procedures for conducting air quality analyses. Principals of the MOU are to:
– Establish agreed upon procedures for conducting air quality analyses, formal stakeholder input process, and dispute resolution procedures
– Reduce the costs to both agencies and development project proponents through promotion of modeling techniques which allow for leveraging i ti l i t th t t ti lexisting analysis to the extent practical
• Reduction of the burden in modeling can occur through two approaches:
1. Establishing a reusable modeling framework – regional air quality analyses that bracket development potential in a given airshed that can be leveragedthat bracket development potential in a given airshed that can be leveraged to describe potential impacts for an individual project
2. Promoting use of single modeling platforms to the extent practical to deal with ozone and PM2 5 NAAQS and AQRV requirements of NEPA. 2.5 q
Where Does EPA and FLM’s Go From Here?
• NEPA requirements and Sierra Club petition equ e e ts a d S e a C ub pet t onecessitate that both FLM’s and EPA reassess the suitability of the existing modeling paradigm to
• In order to address these needs, the EPA and FLM’s undertook a project to compare the model
di ti f i ti d l d ipredictions of existing models and emerging models to understand both the predicted impacts for resource management decisions and to betterfor resource management decisions and to better understand the resource requirements and challenges to implementation.
EPA WA Task 6: lSingle‐Source LRT Demonstration
• Apply LRT chemical dispersion models for example test sources as one would for a PSD far field Class I assessmentone would for a PSD far‐field Class I assessment– 2005 and 2006 annual simulations examined– CALPUFF/CALMET and CALPUFF/MMIF– CAMx using PSAT/APCA source apportionment– CAMx using PSAT/APCA source apportionment
• Compare far‐field air quality and air quality related values (AQRVs) metrics at Class I areas across LRT dispersion models– Maximum concentrations SO2 NO2 PM10)Maximum concentrations SO2, NO2, PM10)– Maximum visibility impairment (FLAG, 2010)– Maximum sulfur and nitrogen deposition
• This presentation documents LRT dispersion model simulations and consequence analyses performed by ENVIRON under contract to EPA in 2011ENVIRON under contract to EPA in 2011.
7
Task 6: Single‐Source LRT Model Demonstration
• 2005 12/4 km FCAQTF • 2006 12 km UT‐CO720 2005 12/4 km FCAQTF 2006 12 km UT CO
240
360
480
600
720
360
-240
-120
0
120
-840
-720
-600
-480
-360
12 km
4 km
-2280-2160-2040-1920-1800-1680-1560-1440-1320-1200-1080 -960 -840 -720 -600 -480 -360
New Mexico CAMx 12 km Nested Domain
IMPROVECASTNET
12 km
8
CASTNETNADP
CAMx 12 km: 167 x 137* (-2316, -912) to ( -312, 732)CAMx 04 km: 101 x 92* (-1192, -508) to ( -788, -140)
* includes buffer cells
Test Sources
2005 FCAQTF 12/4 km
• 5 EGU Point Sources
• 9 oil and gas point and g parea source areas– 9 x 9 4 km area sources
Any point sources in– Any point sources in region
9
T t STest Sources2006 12 km UT‐CO
• 13 EGU Point Sources
• 11 oil and gas point and area source areas– 3 x 3 12 km grid cells– Any point sources in regionregion
10
2005 4 km Annual NO2 (top) and SO2 (bottom) at Class I receptors: FCAQTF(bottom) at Class I receptors: FCAQTFCALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CAMx vs. CALPUFF/MMIF
y = 1.0469x - 0.00240.6
Annual NO2 (ug/m3)
y = 0.6521x - 0.0020.6
Annual NO2 (ug/m3)
y = 1.5724x + 0.00160.6
Annual NO2 (ug/m3)
0.2
0.3
0.4
0.5
CAM
x N
O2
(ug/
m3)
0.2
0.3
0.4
0.5
PU
FF/M
MIF
NO
2 (u
g/m
3)
0.2
0.3
0.4
0.5
CAM
x N
O2
(ug/
m3)
0
0.1
0 0.1 0.2 0.3 0.4 0.5 0.6CALPUFF/CALMET NO2 (ug/m3)
0
0.1
0.0 0.1 0.2 0.3 0.4 0.5 0.6
CAL
CALPUFF/CALMET NO2 (ug/m3)
0
0.1
0 0.1 0.2 0.3 0.4 0.5 0.6CALPUFF/MMIF NO2 (ug/m3)
y = 1.0708x - 0.0004
0.4
0.5
0.6
m3)
Annual SO2 (ug/m3)
y = 0.7204x - 0.0043
0.25
0.3
0.35
0.4
(ug/
m3)
Annual SO2 (ug/m3)
y = 1.4737x + 0.0064
0.4
0.5
0.6
m3)
Annual SO2 (ug/m3)
0.1
0.2
0.3
CAM
x SO
2 (u
g/m
0.05
0.1
0.15
0.2
CALP
UFF/
MM
IF S
O2
0.1
0.2
0.3
CAM
x SO
2 (u
g/m
11
00 0.1 0.2 0.3 0.4 0.5 0.6
CALPUFF/CALMET SO2 (ug/m3)
00 0.1 0.2 0.3 0.4
CALPUFF/CALMET SO2 (ug/m3)
00 0.1 0.2 0.3 0.4 0.5 0.6
CALPUFF/MMIF SO2 (ug/m3)
2005 4 km 24‐hr (top) and 3‐hr (bottom) SO2 at Class I receptors: FCAQTFSO2 at Class I receptors: FCAQTF
CALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CAMx vs. CALPUFF/MMIF
1 2049 0 0602
14
High 1st High 24-hour SO2 (ug/m3)
14
High 1st High 24-hour SO2 (ug/m3)
y 1 8391x + 0 1091
14
High 1st High 24-hour SO2 (ug/m3)
y = 1.2049x - 0.0602
6
8
10
12
CAM
x SO
2 (u
g/m
3)
y = 0.6557x - 0.0925
6
8
10
12
FF/M
MIF
SO
2 (u
g/m
3)
y = 1.8391x + 0.1091
6
8
10
12
CAM
x SO
2 (u
g/m
3)
0
2
4
0 2 4 6 8 10 12 14CALPUFF/CALMET SO2 (ug/m3)
0
2
4
0 2 4 6 8 10 12 14
CALP
UF
CALPUFF/CALMET SO2 (ug/m3)
0
2
4
0 2 4 6 8 10 12 14CALPUFF/MMIF SO2 (ug/m3)
y = 0.5839x + 0.083
30
35
40
45
3)
High 1st High 3-hour SO2 (ug/m3)
y = 0.6641x - 0.4691
30
35
40
45
g/m
3)
High 1st High 3-hour SO2 (ug/m3)
y = 0.8636x + 0.53
30
35
40
45
3)
High 1st High 3-hour SO2 (ug/m3)
5
10
15
20
25
CAM
x SO
2 (u
g/m
3
5
10
15
20
25
CALP
UFF/
MM
IF S
O2
(ug
5
10
15
20
25
CAM
x SO
2 (u
g/m
3
12
0
5
0 5 10 15 20 25 30 35 40 45CALPUFF/CALMET SO2 (ug/m3)
0
5
0 5 10 15 20 25 30 35 40 45CALPUFF/CALMET SO2 (ug/m3)
0
5
0 5 10 15 20 25 30 35 40 45CALPUFF/MMIF SO2 (ug/m3)
2005 4 km ann (top) and 24‐hr (bottom) PM10 at Class I receptors: FCAQTFPM10 at Class I receptors: FCAQTF
CALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CAMx vs. CALPUFF/MMIF
y = 0.2624x + 0.0006
0 25
0.3
Annual PM10 (ug/m3)
y = 0.6922x - 0.0009
0 25
0.3
Annual PM10 (ug/m3)
y = 0.374x + 0.001
0 25
0.3
Annual PM10 (ug/m3)
0.1
0.15
0.2
0.25
CAM
x PM
10 (
ug/m
3)
0.1
0.15
0.2
0.25
ALP
UFF/
MM
IF P
M10
(ug/
m3)
0.1
0.15
0.2
0.25
CAM
x PM
10 (
ug/m
3)
0
0.05
0 0.05 0.1 0.15 0.2 0.25 0.3CALPUFF/CALMET PM10 (ug/m3)
0
0.05
0 0.05 0.1 0.15 0.2 0.25 0.3
CA
CALPUFF/CALMET PM10 (ug/m3)
0
0.05
0 0.05 0.1 0.15 0.2 0.25 0.3CALPUFF/MMIF PM10 (ug/m3)
High 1st High 24-hour PM10 (ug/m3) High 1st High 24-hour PM10 (ug/m3) High 1st High 24-hour PM10 (ug/m3)
y = 0.1745x + 0.0389
3
3.5
4
4.5
5
0 (u
g/m
3)
y = 0.6266x - 0.0111
3
3.5
4
4.5
5
PM10
(ug/
m3)
y = 0.2646x + 0.0466
3
3.5
4
4.5
5
0 (u
g/m
3)
0
0.5
1
1.5
2
2.5
0 0 5 1 1 5 2 2 5 3 3 5 4 4 5 5
CA
Mx
PM
10
0
0.5
1
1.5
2
2.5
0 0 5 1 1 5 2 2 5 3 3 5 4 4 5 5
CA
LPU
FF/M
MIF
P
0
0.5
1
1.5
2
2.5
0 0 5 1 1 5 2 2 5 3 3 5 4 4 5 5
CA
Mx
PM
10
13
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 5CALPUFF/CALMET PM10 (ug/m3)
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 5CALPUFF/CALMET PM10 (ug/m3)
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 5CALPUFF/MMIF PM10 (ug/m3)
Different PM10 species mappings used w/ CALPUFF vs. CAMx/PSAT
2006 12 km annual NO2 (top) and SO2 (bottom) at Class I receptors: UT‐CO(bottom) at Class I receptors: UT COCALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CAMx vs. CALPUFF/MMIF
y = 0.0672x + 0.00912.8
3
3.2
Annual NO2 (ug/m3)
y = 0.2962x + 0.00642.8
3
3.2
Annual NO2 (ug/m3)
y = 0.4987x + 0.00462.8
3
3.2
Annual NO2 (ug/m3)
0 8
1
1.2
1.4
1.6
1.8
2
2.2
2.4
2.6
CAM
x NO
2 (u
g/m
3)
0 8
1
1.2
1.4
1.6
1.8
2
2.2
2.4
2.6
CALP
UFF/
MM
IF N
O2
(ug/
m3)
0 8
1
1.2
1.4
1.6
1.8
2
2.2
2.4
2.6
CA
Mx
NO
2 (u
g/m
3)
0
0.2
0.4
0.6
0.8
0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2
CALPUFF/CALMET NO2 (ug/m3)
0
0.2
0.4
0.6
0.8
0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 2.6 2.8 3.0 3.2
C
CALPUFF/CALMET NO2 (ug/m3)
0
0.2
0.4
0.6
0.8
0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2
CALPUFF/MMIF NO2 (ug/m3)
Annual SO2 (ug/m3) Annual SO2 (ug/m3) Annual SO2 (ug/m3)
y = 0.389x + 0.003
0.2
0.25
0.3
0.35
0.4
2 (u
g/m
3)
y = 0.4628x + 0.0021
0.2
0.25
0.3
0.35
0.4
IF S
O2
(ug/
m3)
y = 0.9331x + 0.0008
0.2
0.25
0.3
0.35
0.4
2 (u
g/m
3)
0
0.05
0.1
0.15
0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4
CAM
x S
O2
CALPUFF/CALMET SO2 (ug/m3)
0
0.05
0.1
0.15
0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4
CAL
PUF
F/M
MI
0
0.05
0.1
0.15
0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4
CAM
x S
O2
14
CALPUFF/CALMET SO2 (ug/m3) CALPUFF/CALMET SO2 (ug/m3) CALPUFF/MMIF SO2 (ug/m3)
Very high CALPUFF/CALMET (CALPUFF/MMIF) outlier
2006 12 km 24‐hr (top) and 3‐hr (bottom) SO2 at Class I receptors: UT‐CO(bottom) SO2 at Class I receptors: UT CO
CALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CAMx vs. CALPUFF/MMIF
4
High 1st High 24-hour SO2 (ug/m3)
4
High 1st High 24-hour SO2 (ug/m3)
4
High 1st High 24-hour SO2 (ug/m3)
y = 0.3689x + 0.0205
1 5
2
2.5
3
3.5
AM
x SO
2 (u
g/m
3)
y = 0.5301x + 0.0224
1 5
2
2.5
3
3.5
FF/M
MIF
SO
2 (u
g/m
3)
y = 0.6652x + 0.0077
1 5
2
2.5
3
3.5
AM
x SO
2 (u
g/m
3)
0
0.5
1
1.5
0 0.5 1 1.5 2 2.5 3 3.5 4
CA
CALPUFF/CALMET SO2 (ug/m3)
0
0.5
1
1.5
0 0.5 1 1.5 2 2.5 3 3.5 4
CAL
PUF
CALPUFF/CALMET SO2 (ug/m3)
0
0.5
1
1.5
0 0.5 1 1.5 2 2.5 3 3.5 4
CA
CALPUFF/MMIF SO2 (ug/m3)
y = 0.2432x + 0.046
10
12
14
)
High 1st High 3-hour SO2 (ug/m3)
y = 0.4807x + 0.0735
10
12
14
ug/m
3)
High 1st High 3-hour SO2 (ug/m3)
y = 0.5059x + 0.0088
10
12
14
)
High 1st High 3-hour SO2 (ug/m3)
2
4
6
8
CAM
x SO
2 (u
g/m
3)
2
4
6
8
CALP
UFF/
MM
IF S
O2
(u
2
4
6
8
CAM
x SO
2 (u
g/m
3)
15
00 2 4 6 8 10 12 14
CALPUFF/CALMET SO2 (ug/m3)
00 2 4 6 8 10 12 14
CALPUFF/CALMET SO2 (ug/m3)
00 2 4 6 8 10 12 14
CALPUFF/MMIF SO2 (ug/m3)
2006 12 km CALPUFF High “Outlier”2006 12 km CALPUFF High Outlier
• Maximum annual NO2 and SO2 by CALPUFF/CALMET a u a ua O a d SO by U /occurs for smallest EGU12 (13 TPY NOX and 1 TPY SO2)
• EGU12 located within Holy Cross Wilderness (Class II area) so likely nearly co‐located with receptors
• Maximum CALMET, MMIF and CAMx annual NO2 t ticoncentrations:
– 3.1; 0.6; and 0.02 µg/m3
• We understand why CALMET much higher than CAMx• We understand why CALMET much higher than CAMx– CAMx configured for LRT application with 12 km grid
• Why MMIF and CALMET so different?y
16
EGU12 Holy Cross Wilderness OutlierEGU12 Holy Cross Wilderness Outlier
• CALMET modifying and slowing MM5 windsy g g• Occurs at the surface and aloft• Unclear whether diagnostic effects or
( )observation Objective Analysis (OA) procedure is doing this
• Occurs throughout the year• Occurs throughout the year• Results in very high concentrations in CALPUFF/CALMET/
• Better agreement with CAMx and CALPUFF/CALMET at other sites
19
2005 (top) and 2006 (bottom) VisibilityCALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CALPUFF/MMIF vs. CAMx
y = 0.2301x + 0.3492
40
45
50
High 1st High Extinction from Sources (Mm-1)
y = 0.6296x - 0.0007
40
45
50
High 1st High Extinction from Sources (Mm-1)
y = 0.3452x + 0.3991
40
45
50
High 1st High Extinction from Sources (Mm-1)
15
20
25
30
35
CAM
x B
ext
(Mm
-1)
15
20
25
30
35
PUFF
/MM
IF B
ext (
Mm
-1)
15
20
25
30
35
CAM
x B
ext
(Mm
-1)
0
5
10
15
0 5 10 15 20 25 30 35 40 45 50CALPUFF/CALMET Bext (Mm-1)
0
5
10
15
0 5 10 15 20 25 30 35 40 45 50
CALP
CALPUFF/CALMET Bext (Mm-1)
0
5
10
15
0 5 10 15 20 25 30 35 40 45 50CALPUFF/MMIF Bext (Mm-1)
CALPUFF/CALMET vs. CAMx CALPUFF/CALMET vs. CALPUFF/MMIF CALPUFF/MMIF vs. CAMx
y = 0.6632x + 0.093940
45
High 1st High Extinction from Sources (Mm-1)
y = 0.7572x + 0.258840
45
High 1st High Extinction from Sources (Mm-1)
y = 0.6034x + 0.17740
45
High 1st High Extinction from Sources (Mm-1)
15
20
25
30
35
CAM
x Be
xt (
Mm
-1)
15
20
25
30
35
PUFF
/MM
IF B
ext (
Mm
-1)
15
20
25
30
35
CAM
x Be
xt (
Mm
-1)
200
5
10
0 5 10 15 20 25 30 35 40 45CALPUFF/CALMET Bext (Mm-1)
0
5
10
0 5 10 15 20 25 30 35 40 45
CAL
CALPUFF/CALMET Bext (Mm-1)
0
5
10
0 5 10 15 20 25 30 35 40 45CALPUFF/MMIF Bext (Mm-1)
2005 4 km Maximum Visibilityy• Spatial variability across receptors (CALPUFF) and grid cells that intercept Class I area– Except for close source‐receptors, variability similar
21
Nitrogen Deposition (kg‐N/ha/yr)
• CAMx N deposition much• CAMx N deposition much greater (factor of ~2) than CALPUFF
• CALPUFF/MMIF N deposition slightly greater than CALPUFF/CALMETCALPUFF/CALMET
22
Sulfur Deposition (kg‐S/ha/yr)
• Sulfur deposition comparable– CAMx > CALPUFF/CALMET
– CPUFF/MMIF > CALPUFF/CALMET– CPUFF/MMIF > CALPUFF/CALMET
– Except for one point: CAMx=CALPUFF/MMIF
( i il lt f 2006)• (similar results for 2006)
23
Why CAMx Estimating Higher N Deposition than CALPUFF?
• Different species mappings with CAMx more N species and only including NH4 from test source and CALPUFF including NH4 assuming SO4/NO3 neutralizedassuming SO4/NO3 neutralized
• Performed CAMx species mapping using CALPUFF rules– Wrong direction for large sources
0.3000.4000.5000.600
‐N/ha]
Annual Nitrogen Deposition (Wet + Dry)EGU1
camx
camx puffN
calpuff
– Not enough small sources
0.0000.1000.200
ande
lier N
M
La Garita
Wild
erne
ss
sa Verde
NP
rifie
d Forest
NP
Pedro Parks
Wild
Wem
inuche
Wild
erne
ss
[kg‐
calpuff mmif
Annual Nitrogen Deposition (Wet + Dry)EGU3
Ba
Mes
Petr
San P W W
Class I Area
0.0000.0050.0100.0150.0200.0250.0300.035
M a ss NP
NP ks
he
ss
[kg‐N/ha]
EGU3
camx
camx puffN
calpuff
calpuff mmif
Band
elier N
M
La Garita
Wild
erne
Mesa Ve
rde N
Petrified
Forest N
San Pedro Park
Wild
Wem
inuch
Wild
erne
s
Class I Area24
Why CAMx estimating higher N Deposition than CALPUFF?Why CAMx estimating higher N Deposition than CALPUFF?
• CAMx carrying more N as nitric acid (HNO3)y g ( )• CALPUFF carrying more N as particle nitrate (NO3)
• CALPUFF default ammonia background 10 ppb• CAMx simulates ammonia/ammonium
Typically estimates values << 1 ppb in high terrain of– Typically estimates values << 1 ppb in high terrain of Rocky Mountains
• More representative of measurements (e.g., Dinosaur National Monument)National Monument)
• Revised CALPUFF runs with more realistic background ammonia
25
Barriers to Implementation ‐lComputational
• The modeling platforms for the permit modelingThe modeling platforms for the permit modeling community are largely Microsoft Windows based and are engineered for serial applications of models.
• The meteorological and photochemical modeling community is largely Unix/Linux based.
• Time necessary for annual PGM simulations compared to current model recommended for AQRV
lanalyses.
Computational ConsiderationsComputational Considerations
• Adaptation of the PGM platforms to operate in a Windows p p pbased environment?– The permit modeling community typically does not have the same
level of fluency in either the Unix/Linux operating system or Fortranlevel of fluency in either the Unix/Linux operating system or Fortran based programming skills that are essential skill requisites
– IT authorities within State and Local permitting agencies often lack the familiarity and/or resources to dedicate to systems administration andfamiliarity and/or resources to dedicate to systems administration and security for Unix/Linux based systems, and thus actively prevent the acquisition of such equipment or, if such hardware is acquired, prevent the presence of such equipment on the State’s internal p p q pnetwork.
Barriers to Implementation ‐lRegulatory
• The operational construct for the permit modeling community is highly rigidcommunity is highly rigid– Based upon a series of regulations and guidelines which restrict operational flexibility in order to promote more general consistency in the application of modelsgeneral consistency in the application of models.
• The operational construct of the meteorological and photochemical modeling communities is vastly diffdifferent– Based upon a more loosely binding set of EPA recommendations which typically encourage adapting b h d d l h d hboth science and modeling techniques to produce the most scientifically feasible answer given the constraints of the state‐of‐the‐science.
Regulatory ConsiderationsRegulatory Considerations
• The differences in the operational paradigms between the two communities will require both the EPA and the FLM’s to develop a more rigid set of operational procedures similar to the current permit modeling paradigm in order to insure both a scientifically sound and consistent set of procedures to prevent an ‘anything goes’ process as would likely develop without such procedures.p
• Length of meteorological record for PGM’s will likely have to be expanded to be consistent with requirements of GAQM (e g 3 years of prognostic data)(e.g. 3 years of prognostic data).
• Development of significance thresholds for single source (cause or contribute test) required for NAAQS demonstrationsdemonstrations.
ConclusionConclusion
• PGM’s capable of assessing single source impacts for both p g g pAQRV and ozone requirements under PSD.
• Source apportionment eliminates need for multiple “zero‐t”out” runs
• Significant barriers remain to implementation of PGM’s
– Increased computational requirementsIncreased computational requirements
– Increased training requirements for permit modeling staff
– Creation of a hybrid regulatory and guidance framework y g y gfor implementation of PGM’s within a regulatory permit modeling paradigm which is highly rigid and prescriptive