Indian Network Project on Carbonaceous Aerosol Emissions ...
Transcript of Indian Network Project on Carbonaceous Aerosol Emissions ...
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https://doi.org/10.1175/BAMS-D-19-0030.2 Corresponding author: Chandra Venkataraman, [email protected] document is a supplement to https://doi.org/10.1175/BAMS-D-19-0030.1In final form 3 January 2020©2020 American Meteorological SocietyFor information regarding reuse of this content and general copyright information, consult the AMS Copyright Policy.
SupplementIndian Network Project on Carbonaceous Aerosol Emissions, Source Apportionment and Climate Impacts (COALESCE)C. Venkataraman, M. Bhushan, S. Dey, D. Ganguly, T. Gupta, G. Habib, A. Kesarkar, H. Phuleria, and R. Sunder Raman
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Details of survey methodology and locationsThis project with 22 institutions (Fig. ES1) involves participation of 40 investiga-tors (Table ES1) and most importantly, over 70 research students and staff. Sur-vey questionnaires were adapted from previously validated instruments for residential sector (Census 2011; Interna-tional Institute of Population Science, 2007, 2017; Balakrishnan et al. 2004), agricultural residue burning (Gupta 2014), brick kilns (Maithel et al. 2012; S. Maithel 2017, personal communica-tion), and on-road vehicles (Table ES2; Goel et al. 2015; S. K. Guttikunda 2016, personal communication). Selection of the survey districts/villages to capture the pan-India diversity in biomass fuels used for cooking, heating, and lighting in residential sector is based on district/village level data (Census 2011), along with agroclimatic information (Basu and Guha 1996) for residential cooking; that in agricultural residue burning practices is based on district-wise crop production data (OGDP 2015) of nine target crops (Pandey et al. 2014; Sahai et al. 2011; Jain et al. 2014), different key brick kiln technologies, and a variety of fuel mixes (Table ES3; TERI 2002; Development Alternatives 2012; Maithel et al. 2012; Verma and Uppal 2013; Weyant et al. 2014; SAMEEEKSHA 2018).
Details of field measurement campaignsField measurements of aerosol emissions are planned using a design of a portable source sampler adapted from previous work (Jaiprakash et al. 2016; Jaiprakash and Habib 2018a,b) using the carbon balance method. The design and performance of portable dilution sampler is detailed in Jaiprakash et al. (2016). The modified sampler for this project will consist of an inlet, a heated duct, a dilution tunnel of 3-L capacity (diameter = 10 cm and length = 40 cm) which provides maximum dilution ratio 1:100 at 3-s residence time to achieve complete gas-to-particle partitioning, clean air generation system, and power supply unit (Fig. ES2). For residential cookstove and open biomass burning a multiarm inlet will be used to withdraw the emissions mixed with background air that will be collected on filters and a fraction will enter into a dilution tunnel which would be connected to real-time measurement instru-ments (aethalometer, nephelometer, and optical particle spectrometer). In case of vehicular and brick kiln emission measurement, the emissions will be withdrawn using a heated particle sampling probe working on ejector technique and will be collected on filters after dilution in the primary dilution tunnel. Then a fraction of diluted exhaust will enter into the secondary dilution tunnel where further dilution will take place before the real-time measurement using aethalometer, nephelometer, and optical particle spectrometer. The source sampler will also include a PM sampler consisting of PM2.5 sharp cut cyclone and filter holders for particle, a flue gas analyzer for measurement of gaseous pollutants (CO,
Fig. ES1. COALESCE organization structure.
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Table ES1. List of participating institutions and investigators. Names of principal investigators of the respective institutions are in bold.
Sr. No Name Affiliation Institute
1 Chandra Venkataraman (National Coordinator)
Professor, Department of Chemical Engineering; Associate faculty, IDP in Climate studies
IIT Bombay2 Mani Bhushan Professor, Department of Chemical Engineering; Associate faculty, IDP in Climate studies
3 Harish Phuleria Assistant Professor, Centre for Environmental Science and Engineering; Associate faculty, IDP in Climate studies
5 Tarun Gupta Professor, Department of Civil Engineering
IIT Kanpur6 Debajyoti Paul Professor, Department of Earth Sciences
7 Anubha Goel Associate Professor, Department of Civil Engineering
8 Gazala Habib Associate Professor, Department of Civil Engineering
IIT Delhi9 S.K. Dash Professor, Centre for Atmospheric Science
10 Sagnik Dey Associate Professor, Centre for Atmospheric Science
11 Dilip Ganguly Assistant Professor, Centre for Atmospheric Science
12 Ramya Sunder Raman Associate Professor, Department of Earth and Environmental Sciences IISER Bhopal
13 R. Ravi Krishna Professor, Department of Chemical Engineering
IIT Madras14 S. M. Shiva Nagendra Professor, Department of Civil Engineering
15 Sachin S. Gunthe Associate Professor, Department of Civil Engineering
16 Shubha Verma Associate Professor, Department of Civil Engineering IIT Kharagpur
17 S. Sajani Senior Scientist, Multi-scale modeling Programme CSIR(4PI),Bangalore
18 S. Ramachandran Professor and Chairperson, Space and Atmospheric SciencesPRL Ahmedabad
19 Harish Gadhavi Scientist-SE, Space and Atmospheric Sciences Division
20 T.K. Mandal Principal Scientist, Radio and Atmospheric Sciences
NPL Delhi21 S.K.Sharma Scientist, Radio and Atmospheric Sciences
22 C. Sharma Sr. Principal Scientist, Radio and Atmospheric Sciences
23 S. Singh Principal Scientist, Radio and Atmospheric Sciences
24 G. Pandithurai Scientist F IITM Pune
25 Baerbel Sinha Assistant Professor, Environmental Science IISER Mohali
26 Arshid Jehangir Sr. Assistant Professor, Environmental Science University of Kashmir
27 Amit Kesarkar Scientist-SE, Weather and Climate Research GroupNARL
28 Vikas Singh Scientist-SD, Weather and Climate Research Group
29 R. Naresh Kumar Assistant Professor, Department of Civil and Environmental EngineeringBITS Mesra
30 Jawed Iqbal Assistant Professor, Department of Civil and Environmental Engineering
31 Asif Qureshi Assistant Professor, Department of Civil Engineering IIT Hyderabad
32 Abhijit Chatterjee Associate Professor, Environmental Science Section
Bose Institute, Darjeeling33 Sanjay K Ghosh Professor, Department of Physics
34 Sibaji Raha Professor, Department of Physics
35 Binoy K Saikia Scientist, Coal Chemistry DivisionCSIR-NEIST, Jorhat
36 Prasenjit Saikia Scientist, Coal Chemistry Division
37 S. Anand Scientist, Health Safety and Environment GroupBARC, Mumbai
38 Tanmay Sarkar Technical Officer, Health Safety and Environment Group
39 Rohini Bhawar Assistant Professor, Department of Atmospheric and Space Sciences University of Pune
40 Anil Kumar Chhangani Head, Department of Environment Science Maharaja Ganga Singh University, Bikaner
41 Jitender Singh Laura Head, Department of Environment Science Maharshi Dayanand University, Rohtak
42 K.S. Lokesh Professor, Department of Environmental Engineering Sri Jayachamarajendra College of Engineering, Mysuru43 Udhayashankar T.H. Professor, Department of Environmental Engineering
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CO2, NOx, SOx, and total hydrocarbons). The exhaust velocity will be measured in the duct using a pitot tube. The dilution ratio inside the dilution tunnel will be calculated using CO2 measurement of undiluted and diluted exhaust following Jaiprakash et al. (2016). Unlike earlier dilution samplers commercially available the present sampler can be operated for a range of dilution ratio 5:1 to 100:1 by varying the clean airflow and suction flow in particle sampling probe. Details of all components and instruments used in the dilution sampler are given in Table ES4.
Equation for the carbon balance method to estimate emission factors (Roden et al. 2006):
EFCO CO kg Cm
CF,xXV
� ��
�
��
�
����
��
�
����
[ ]
.
1 1
0 49052
3� �
where EFX is emission factors of species X [gx (kgfuel)−1], [X] is concentration of species X (g m−3), V is volume of air sampled (m3), ∆CO2 is concentration of CO2 above ambient (ppm), ∆CO is concentration of CO above ambient (ppm), and CF is carbon fraction in fuel [kg C (kgfuel)−1].
Table ES2. Mapping of cities for vehicle survey.
COALESCE institutes State Cities as per tier classification
S1
(Population >
1,000,000)
I (100,000
> population
≤ 1,000,000)
II (50,000
< population
< 99,999)
III (20,000
< population
< 49,999)
IV (10,000
< population
< 19,999)
V (5,000
< population
< 9,999)
VI (population
< 5,000)
No. of surveys
(transport/nontransport)
University of Kashmir J&K Srinagar Jammu Anantnag Bandipore Gulmarg Achabal Banihal 670
IISER Mohali Punjab Chandigarh Amritsar Kapurthala Jalalabad Majitha Maloud Sansarpur 670
IIT DelhiRajasthan Jaipur Ajmer Balotra Bhadra Bhusawar Bhalariya Govindgarh 670
Delhi Ghazaibad East Delhi West Delhi North Delhi South Delhi Central Delhi 670
NPL Delhi Haryana Panipat Ambala Narnaul Charkhi Dadri Bawal Farakhpur Rewari 670
IIT Kanpur Uttar Pradesh kanpur Kanpur Khurja Mahrajganj Manikpur Mohanpur Amila 670
BOSE Institute Bihar Nalanda Patna Samastipur Ramnagar Thakurganj Asarganj N/A 670
NEIST Jorhat Assam Nagaland Dibrugarh Karimganj Nalbari Udalguri Amguri Howraghat 670
IISER Bhopal
Madhya Pradesh Bhopal Vidisha Jaora Multai Shahgarh Tirodi Badra 670
IIT Hyderabad Telangana Telangana Hyderabad Nirmal Naspur Utnur Tangapur Ratnapur 670
Mysore Karnataka Banglore Mandya Hunsur Pandavapura Arasinakunte Kadakola N/A 670
IIT Madras Tamil Nadu Chennai Vellore Arakonam Lalgudi Pudur Puvalur Unjalur 670
IIT Bombay Maharashtra Thane Ghatkopar Kharghar Uran Murbad Kharbav Saphale 670
BIT Mesra Jharkhand Ranchi Hazaribagh Rajrappa Churi Muri Bharno Topa 670
IIT Kharagpur West Bengal Kolkata Kharagpur Jhargram Kolaghat Mandarmani Digha Hariatara 670
IITM Pune Maharashtra Pune Lavasa Talegaon Keshavnagar Panchgani Dehu Adhale kh 670
Kshetra Wai Mahabaleswar Birwadi 670
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Table ES3. State-wise field survey districts for residential (Re), agricultural residue burning (Ag), and brick sectors (Br).
State Districts Re Ag Br State Districts Re Ag Br
J&K
Anantnag
Maharashtra
Chandrapur
Badgam Jalgaon
Baramula Satara
Pulwama Latur
Ganderbal
Jharkhand
Dhanbad
Himachal PradeshSolan Hazaribagh
Una Ranchi
Uttarakhand Udham Singh Nagar
Punjab
Fategarh sahib
West Bengal
Maldah
Firozpur Koch bihar
Sangrur Hugli
Pathankot Bardhman
SAS Nagar
Ropar
Kerala
Thrissur
Wayanad
Haryana
Sonipat
Ambala
Jhajjar
Assam
Nagaon
Panchkula Golpara
Nalbari
Rajasthan
Bikaner
Sikar Meghalaya West Garo Hills
Rajasmand
Sri Ganganagar Nagaland Dimapur
Kota
Dhaulpur
Orissa
Baleshwar
Balangir
Uttar Pradesh
Gorakhpur Cuttack
Bijnor Sundargarh
Bairach
Hardoi
Kushi nagar
Telangana
Nalgonda
Ghaziabad Warangal
Kanpur Medak
Varanasi Sangareddy
ChhattisgarhJanjgir-champa
Andhra Pradesh
Krishna
Raigarh Chittoor
SPSR Nellore
Madhya Pradesh
Jhabua
Hoshangabad
Karnataka
Dakshin Kannada
Sehore Belgaum
Datia Mandya
Rajgarh Kolar
Gujarat
JunagadhTamil Nadu
Theni
Vadodara Dharmapuri
Bhavnagar
AhmedabadBihar
Araria
Surat Bhagalpur
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Equations for estimating emission factors using dilution sampler (Jaiprakash et al. 2016; Lipsky and Robinson 2005):
DRCO
undilutedCO
amb
COdiluted
COamb
�� � � � �� � � � �C C
C C2 2
2 2
,
where DR is dilution ratio, (CCO2)undiluted is concentration of CO2 in undiluted exhaust, (Cco)amb concentration of CO2 in ambient, and (CCO2)diluted is concentration of CO2 after undiluted exhaust
EF g kgDR
or
duct ex
xX A t
F D�� � � � � � �1 [ ]
,�
where EFX emission factor of pollutant X [gx (kgfuel)−1], [X] is concentration of species X (g m−3), Aduct is area of duct (m2), υex is exhaust velocity X (m s–1), t is sampling time (s), F is fuel used (kg), and D is distance traveled by vehicle (km).
Methodologies for the ambient observational networkSelecting regionally representative sites. A key objective of this study is to sample for fine particulate matter (PM2.5) that is representative of a given region and to apportion the sources of the measured PM mass.
The sites selected are such that the measurements made at these sites will normally be consistent with measurements made at locations separated by 100–500 km from each of these sites. All sites are located such that they capture regionally representative aerosol,
Fig. ES2. Schematic of the source sampling train for on-field measurements. A multiarm inlet (Roden et al. 2006) will be used when used for residential agricultural residue sector measurements and a nozzle inlet along with primary dilution tunnel (Lipsky and Robinson 2005) for vehicular and brick kiln sectors.
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Table ES4. Description and technical specifications of monitoring instruments used for source sampling.
Monitoring instruments
Measurement technique Measurement
Measurement range
Sample interval
Accuracy (resolution) Resolution Reference
Heated sampling probe
Iso-kinetic (TSI) As inlet 0–20 m s−1 — — — —
Portable dilution tunnel
(Polltech Ins. Pvt. Ltd, India)
For dilution 1:100 — — —Jaiprakash
et al. (2016)
Pitot tube (Testo, Sparta, NJ)Velocity
measurement0–100 m s−1 1 s ±0.2 m s−1 0.1 m s−1 —
Flue gas emission analyzer
Electrochemical sensor/NDIR (350, Testo, Sparta, NJ)
O2 0%–25%
1 s
±0.1%–0.8% 0.01%
Jaiprakash et al. (2016)
CO2 (NDIR) 0%–50% ±0.3% to 0.5% 0.1%
CO 0–10,000 ppm ±5 ppm 1 ppm
SOx 0–5,000 ppm ±5 ppm 1 ppm
NO 0–4,000 ppm ±5 ppm 1 ppm
NO2 0–500 ppm ±5 ppm 0.1 ppm
HC (NDIR) 100–40,000 ppm±10% for
>4,000 ppm10 ppm
Temperature 0°–1,000°C ±0.5°C 0.1°C
Temperature probe
Sensor (Testo, Sparta, NJ)
Temperature 0°–70°C 1 s ±0.2°C 0.1°CJaiprakash
et al. (2016)
Relative humidity
Sensor (Testo, Sparta, NJ)
Relative humidity
0%–100% RH 1 s ±2% 0.7%Jaiprakash
et al. (2016)
Diluted CO2 analyzer
Sensor (Testo, Sparta, NJ)
Diluted CO2 0–10,000 ppm 1 s±100 ppm of CO2 ± 3%
value1 ppm
Jaiprakash et al. (2016)
Zero air assembly
(Polltech Ins. Pvt. Ltd, India)
For dilution air 30 LPM — — — —
Multistream PM2.5 Cyclone (URG Based)
Cyclone (URG Corporation, USA)
PM2.5 filter mass
10 LPM — — —Jaiprakash et al.
(2016)
Rechargeable battery+ DC adapter
Sony Power supply 1.5 V — — — —
GPS + datalogger
Vehicle testing (Racelogic, U.K.)
Speed
0.2–150 km h−1 1 s
0.2 km h−1 0.01 km h−1
VBOX Mini user guide
Distance <50 cm 1 cm
Acceleration ±1 m s−2 0.01 1 m s−2
Aerosol spectrometer
Laser light scattering (TSI 3330)
Number concentration
0–3,000 cm−3
1 s 0.01%5% at 0.5 µm
—Number size distribution
0.001– 275,000 µg m−3
0.3–10 µm (16 bins)
Aethalometer
Filter based attenuation
(Magee Scientific AE 33)
Black carbon and absorption coefficients
<0.1 to >100 µg m−3
1 s or 1 min
1 ng m−3 —Magee
Scientific User Manual
Integrating nephlometer
Laser light scattering
(Air Photon IN 102)
Aerosol scattering
coefficients
0–20,000 Mm−1 (−30° to +45°C)
Automatic scanning
— —Air Photon
User Manual
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that is, outside urban centers and away from local pollution sources including but not lim-ited to diesel, cookstove/wood smoke, agricultural field burning, automobile, road dust, or construction dust emissions. Further, these sites are also not located in places with unusual/nonrepresentative meteorology (such as in a valley) for a given region. A weight of evidence approach (Lekinwala et al. 2020), including physical siting criteria, trajectory ensemble, and wind-rose approaches, along with a suite of statistical approaches has been used to identify “regional” sites.
Choice of sampler, filter substrates, and chemical analyses techniques. The Speciation Air Sampling System (SASS; Met One Instruments Inc., Oregon, United States) was deployed to collect samples for the chemical and gravimetric analysis of PM2.5 particles, from its use in earlier networks (in the U.S. EPA Speciation Trends Network and now Chemical Speciation Network). The sampler configuration (Table ES5) is consistent with collecting samples that are required to meet the project goals. Aerosol samples will be collected every other day for 2 years, from January 2019. Meteorological sensors (Met One Instruments Inc., model AIO 2) will also acquire data and will be operated in conjunction with the SASS during each sampling event.
The sampler is configured such that acidic gases are denuded prior to collection onto the nylon substrate (channel 2). Additionally, it is well established that measurement of atmo-spheric particulate matter organic carbon with quartz filter substrates is likely to result in positive artifacts (absorption of organic carbon gaseous species, onto filters) and negative artifacts (volatilization of particle phase semivolatile organic compounds after captured by filters; Turpin et al. 2000). It is proposed to correct for positive artifacts by sampling with two quartz filters in series (QbQ, channel 3). This backup filter will be used to correct for the absorption/adsorption of gaseous organic compounds on the front quartz filters (McDow and Huntzicker 1990; Turpin et al. 1994; Hart and Pankow 1994; Kim et al. 2001). A summary of the filter substrates, analytes, chemical analyses methods, and instruments is presented in Table ES5.
Quality assurance/quality control (QA/QC) plan. Data quality for any study has several dimensions, but the primary goal should be usefulness to data users and understanding of the dataset’s characteristics. All flow audits and performance checks for the SASS sampler
Table ES5. Summary of SASS configuration, filter type, and analytical method for quantification of different constituents present in the source and ambient aerosol samples.
Channel Filter AnalyteAnalytical method
Instrument model/make
1
Teflon
PM2.5 Mass, Elements (Al, Si, P, S, Cl, K, Ca, Sc,Ti, V,Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Rb, Sr, Mo, Cd, Sn, Sb, I, Ba, Hg, Pb, Bi, Ga,
Ge, Y, Zr, In, Te, Cs)
Gravimetry, ED-XRF and ICP OES
Sartorius microbalance CP5, PAN alytical Epsilon 4 and Analytik Jena Plasma
Quant PQ 9000
2Nylon with
denuder
Water soluble inorganic ions
Ion chromatographyThermo Dionex Dual
ICS-AquionCation (Li+, Na+, NH4
+, K+, Ca+2, Mg+2)
Anion (F−, Cl−, NO2−, Br−, NO3
−, PO43−, SO4
2−)
3Quartz behind
quartz
Organic and elemental carbon fraction (OC1, OC2, OC3, OC4, EC1, EC2, EC3) and
brown carbon
Thermal-optical analysis
DRI-2015 Multi-Wavelength Thermal Carbon Analyzer
4Quartz behind
quartz
Volatile organics and organic molecular markers for secondary organic aerosols
(SOA), C-13 isotope
GC-MS and IRMS/ MC-ICPMS
Agilent 7890B Gas Chromatograph–Mass
Spectrophotometer
5 Teflon Archival
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are being conducted in accordance with manufacturer recommended standard operating and maintenance procedures. Several metrics are considered for assessing the quality of the chemical species measurements. A few examples of the metrics/parameters that will be used in this study for QA/QC include:
1) Accuracy—All analyses will be standardized to reference values that are traceable to NIST or similar standards.
2) Precision—Measured both at individual laboratories and the whole network through regular QC replicates, results from multiple channels at the same site, and interlaboratory blind sample comparisons.
3) Completeness—Data completeness (>95%) will be monitored at all locations4) Sensitivity/detection—The method detection limits (MDLs) and limit of detection (LOD) will
be reported for every analyte measured at all of the chemical and gravimetric analyses laboratories.
Additionally, laboratory blanks, field blanks, spikes, and replicate samples will be used as a part of QA/QC of all analytes.
Details of participating GCMs and RCMsParticipating RCMs include WRF-CHEMERE, WRF-Chem, WRF-CMAQ, RegCM, and GEOS-Chem, which have differences in atmospheric chemistry mechanisms, aerosol physics, and meteo-rological physics schemes (Table ES6). Aerosol microphysics schemes include condensation, coagulation, transport, and deposition processes employing different mathematical approaches to treat aerosol dynamics. WRF-CMAQ and WRF-Chem (with the MADE scheme) adopt a “modal” approach, WRF-CHIMERE and WRF-Chem (with MOSAIC) use a “sectional” approach, while GEOS-Chem adopts a bulk approach following the GOCART model. The RegCM model uses a bulk scheme for sulfate, organic carbon, and black carbon with sectional schemes for
Table ES6. Participating regional climate model (RCM) description.
S. No.Model/ research group
Meteorological parameterizations: land surface model (LSM); cumulus parameterization (CP); surface layer (SL); planetary boundary layer (PBL)
Aerosol module (AER); gas-phase chemistry (GC); photolysis (PL); cloud microphysics coupled to aero-sols (CM); radiation schemes (RAD)
1 WRF-Chem LSM: Noah LSM; CP: Grell 3D scheme; SL: Monin–Obukhov similarity theory; PBL: Mellor–Yamada–Janjić
AER: MADE; GC: RADM2; PL: Fast J photolysis; CM:Thompson scheme; RAD: Rapid Radiative Transfer ModelIIT Bombay
2 WRF-Chem LSM: Noah LSM; CP: Grell 3D scheme; SL: Monin–Obukhov similarity theory; PBL: Mellor–Yamada–Janjić
AER: MOSAIC; GC: CBM-Z; PL: Fast J photolysis; CM: Thompson scheme; RAD: Rapid Radiative Transfer Model
IISER Bhopal and NARL, Gadanki
3 RegCM LSM: BATS; CP: Emanuel scheme; PBL: Holtslag scheme
AER: AERO (complete aerosol); RAD: NCAR Community Climate Model Version3IIT Delhi
4 WRF-CHIMERE LSM: Noah LSM; CP: Grell 3D ensemble scheme; SL: MM5 Monin–Obukhov scheme; PBL: Yonsei University (YSU) scheme
AER: Aerosol module; GC: MELCHIOR reduced; PL: Fast-JX; CM: Lin et al. scheme; RAD: Rapid Radiative Transfer Model (RRTM)
IIT Kharagpur
5 GEOS-Chem (0.5° × 0.625°)
LSM: NASA Catchment Land Surface Model; CP: relaxed Arakawa–Schubert; SL: sigma/hybrid vertical grid system; PBL
AER: ISORRPIA II thermodynamic module; GC: GEOS-Chem chemistry mechanisms; RAD: Rapid Radiative Transfer Model(IIT Madras)
6 WRF-CMAQ LSM: Noah LSM; CP: Grell 3D scheme; SL: Monin–Obukhov similarity theory; PBL: Mellor–Yamada–Janjić
AER: AERO5; GC: CB05; PL: CMAQ; RAD: Rapid Radiative Transfer ModelPune University
and NARL, Gadanki
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dust and sea salt, and includes the direct effect of all aerosol species, along with the sulfate indirect effect. The models have different approaches to calcu-late gas to particle conversion; WRF-CMAQ and GEOS-Chem models adopt ISORROPIA for inorganic species, while WRF-Chem uses MARS for inorganic and SORGAM for organic gas to particle conversion. Calculation of aerosol–radiation interac-tions requires the coupling of the aerosol scheme with the shortwave radiation scheme. The radiation transfer module in selected models uses aerosol optical properties (extinction optical depth, single scattering albedo, asymmetry parameter) varying across wavelength bands (e.g., WRF-Chem at 200, 400, 600, and 1,000 nm and WRF-CHIMERE single-scattering albedos and the asymmetry parameter at 400 and 600 nm along with the AOD at 300, 400, and 999 nm). Among the participating RCMs, most allow for the use of more than one scheme for planetary boundary layer and cloud physics in terms of the cumulus parameterization. Lateral boundary conditions for the RCMs will come from the ERA-Interim data for meteorology, with 3DVAR data assimilation every 12 h (Fig. ES3), and chemical boundary conditions will come from MOZART, except for WRF-CHEMERE and GEOS-Chem, which would be using output from LMDZ-INCA and GEOS-Chem global models, respectively.
All participating GCMs but one have interactive aerosol schemes with different levels of complexity (Table ES7). The GCMs with interactive aerosol schemes include all the significant processes influencing the aerosol life cycle, such as precursor gas and particle emissions, gas and aqueous-phase chemistry, nucleation, condensation, coagulation, aging, precipitation scavenging, and dry deposition. The aerosol module in ECHAM6-HAM2 predicts the time evolution of aerosol size distribution through a modal approach, using a superposition of seven lognormal modes, with internal mixing within modes. Aerosol dynamics uses a three-mode modal aerosol module in the CAM5 model, with aerosol species internally mixed within modes and externally mixed between Aitken, accumulation, and coarse modes, with distinct aerosol optical properties for each mode. SPRINTARS, the aerosol module used in NICAM-SPRINTARS, has a prognostic treatment of aerosols from major natural and anthropogenic sources. The NICAM-SPRINTARS model uses a single-moment cloud microphysics scheme, not coupled to aerosols, thus not including the indirect effect of aerosols. The IITM-ESMv2, a state-of-the-art Earth system model from India suitable for studies of long-term climate and particularly the Indian monsoon rainfall, uses prescribed spectral optical properties of aero-sols to estimated aerosol direct radiative forcing in the model simulations. Model simulated variables will be evaluated against observations (Table ES8) from the Indian region as well as observations that are being made at COALESCE network stations.
Fig. ES3. Data assimilation protocol for the regional climate model intercomparsion.
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Table ES7. Participating general circulation model (GCM) description.
S. No.Model/research group
Meteorological parameterizations: land surface model (LSM); cumulus parameterization (CP); surface layer (SL); planetary boundary layer (PBL)
Aerosol module (AER); gas-phase chemistry (GC); photolysis (PL); cloud microphysics coupled to aerosols (CM); radiation schemes (RAD)
1ECHAM6-HAM2 LSM: JSBACH; CP: Tiedtke scheme; SL:
Monin–Obukhov theory; PBL: Mellor–Yamada scheme
AER: Hamburg Aerosol Module; CM: Lohmann scheme; RAD: PSRADIIT Bombay
2CAM5 LSM: CLM4.5;CP: Zhang and McFarlane
scheme ; SL: Similarity theory; PBL: moist turbulence scheme
AER: 3-modal MAM; CM: Morrison two-moment (coupled to aerosol module) ;RAD: Rapid Radia-tive Transfer Model for GCMs (RRTMG)IIT Delhi
3ECHAM6-HAM2 with cus-tomized optical properties
LSM: JSBACH; CP: Tiedtke scheme; SL: Monin–Obukhov theory; PBL: Mellor–Yamada scheme
AER: Hamburg Aerosol Module; CM: Lohmann scheme; RAD: PSRAD
PRL, Ahmedabad
4CESM1.1 LSM: CLM4.5; CP: Zhang and McFarlane
scheme; SL: similarity theory; PBL: moist and dry turbulence scheme
AER: 7-modal MAM; CM: Morrison two-moment (coupled to aerosol module); RAD: Rapid Radia-tive Transfer Model for GCMs (RRTMG)CSIR-4PI
5NICAM-SPRINTARS LSM: MATSIRO; CP: A-S and Prognostic A-S
scheme; SL: Monin–Obukhov theory; PBL: Mellor–Yamada scheme
AER: SPRINTARS; GC: Takemura sulfate chemistry; CM: Lin scheme; RAD: MSTRN-XBARC, Mumbai
6IITM-ESM LSM: Noah LSM, CP: modified simplified
Arakawa–Schubert (SAS) scheme; PBL: Han and Pan scheme
Prescribed optical properties for Aerosols, RAD: RRTM; CM: Zhao and Carr schemeIITM, Pune
Table ES8. Observational data sources for model evaluation.
S. No. ParametersObservation data
source PeriodGlobal/regional/
station data
Resolution
Spatial Temporal
1 Precipitation, temperature IMD gridded 2000–15 India 0.25° × 0.25° Daily, monthly
2 Precipitation, temperature CRU TS3.23 2000–15 Global 0.5° × 0.5° Daily, monthly
3 Precipitation GPCP v2.2 2000–present Global 2.5° × 2.5° Monthly
4 Precipitation TRMM (TMPA-RT)Mar 2000–
presentGlobal
(60°N to 60°S) 0.25° × 0.25° 3-hourly, daily, Monthly
5Aerosol (AOD, SSA,
size distribution)AERONET 2001–present
Station (10 in India)
— Daily, monthly
6Aerosol and cloud
(vertical profiles, others)CALIPSO 2006–present Global
40 km × 40 km, 30 m vertical
Instantaneous, daily, monthly
7Aerosol and cloud
(various parameters)MODIS 1999–present Global 1.0° × 1.0° Daily, monthly
8Aerosol and cloud
(various parameters)MISR 1999–present Global 0.5° × 0.5° Daily, monthly
9 Aerosol and cloud ISCCP 2000–15 Global — Monthly
10 Cloud (various parameters) CloudSat 2006–present Global 2.0° × 2.0°, 480 m vertical
Daily, monthly
11Pressure, temperature, RH, wind
direction, and wind speed.WMO-IGRA
(radiosonde Data)2000–present
Station (62 in India)
At least 10 levels between 1,000
and 100 hPaDaily, monthly
12 Aerosol TOMS 2000–05 Global 1.0° × 1.25° Daily, monthly
13 Aerosol OMI/Aura 2004–present Global 1.0° × 1.0° Daily, Monthly
14 BC surface concentrationPublished literature (aethalometer data)
2000–presentStation
(at least 10)— Daily, monthly
15 BC vertical profilePublished literature
(aircraft measurements)
Selected field campaign during
2000–present
Station (Kanpur, Bangalore, and
Hyderabad)— Daily
A M E R I C A N M E T E O R O L O G I C A L S O C I E T Y J U LY 2 0 2 0 ES268
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