scholarly journals Comparison of vertical aerosol extinction coefficients from in-situ and LIDAR measurements

2015 ◽  
Vol 15 (13) ◽  
pp. 18609-18651
Author(s):  
B. Rosati ◽  
E. Herrmann ◽  
S. Bucci ◽  
F. Fierli ◽  
F. Cairo ◽  
...  
Keyword(s):  
Absorption Coefficient ◽  
Local Time ◽  
Index Of Refraction ◽  
Aerosol Size Distribution ◽  
Aerosol Extinction ◽  
Dynamic Features ◽  
Extinction Coefficients ◽  
Po Valley ◽  
Ground Station

Abstract. Vertical profiles of aerosol optical properties were explored in a case study near the San Pietro Capofiume (SPC) ground station during the PEGASOS Po Valley campaign in the summer of 2012. A Zeppelin NT airship was employed to investigate the effect of the dynamics of the planetary boundary layer at altitudes between ~ 50–800 m above ground. Determined properties included the aerosol size distribution, the hygroscopic growth factor, the effective index of refraction and the light absorption coefficient. The first three parameters were used to retrieve the light scattering coefficient. Simultaneously, direct measurements of both the scattering and absorption coefficient were carried out at the SPC ground station. Additionally, a LIDAR system provided aerosol extinction coefficients for a vertically resolved comparison between in-situ and remote sensing results. First, the airborne results at low altitudes were validated with the ground measurements. Agreement within approximately ±25 and ±20% was found for the dry scattering and absorption coefficient, respectively. The single scattering albedo, ranged between 0.83 to 0.95, indicating the importance of the absorbing particles in the Po Valley region. A clear layering of the atmosphere was observed during the beginning of the flight (until ~ 10 local time) before the mixed layer (ML) was fully developed. Highest extinction coefficients were found at low altitudes, in the new ML, while values in the residual layer, which could be probed at the beginning of the flight at elevated altitudes, were lower. At the end of the flight (after ~ 12 local time) the ML was fully developed, resulting in constant extinction coefficients at all altitudes measured on the Zeppelin NT. LIDAR results captured these dynamic features well and good agreement was found for the extinction coefficients compared to the in-situ results, using fixed LIDAR ratios (LR) between 30 and 70 sr for the altitudes probed with the Zeppelin. These LR are consistent with values for continental aerosol particles that can be expected in this region.

scholarly journals Studying the vertical aerosol extinction coefficient by comparing in situ airborne data and elastic backscatter lidar

2016 ◽  
Vol 16 (7) ◽  
pp. 4539-4554 ◽  
Author(s):  
Bernadette Rosati ◽  
Erik Herrmann ◽  
Silvia Bucci ◽  
Federico Fierli ◽  
Francesco Cairo ◽  
...  
Keyword(s):  
Absorption Coefficient ◽  
Aerosol Particle ◽  
Index Of Refraction ◽  
Aerosol Extinction ◽  
Hygroscopic Growth ◽  
Dynamic Features ◽  
Extinction Coefficients ◽  
Po Valley ◽  
Ground Station

Abstract. Vertical profiles of aerosol particle optical properties were explored in a case study near the San Pietro Capofiume (SPC) ground station during the PEGASOS Po Valley campaign in the summer of 2012. A Zeppelin NT airship was employed to investigate the effect of the dynamics of the planetary boundary layer at altitudes between ∼  50 and 800 m above ground. Determined properties included the aerosol particle size distribution, the hygroscopic growth factor, the effective index of refraction and the light absorption coefficient. The first three parameters were used to retrieve the light scattering coefficient. Simultaneously, direct measurements of both the scattering and absorption coefficient were carried out at the SPC ground station. Additionally, a single wavelength polarization diversity elastic lidar system provided estimates of aerosol extinction coefficients using the Klett method to accomplish the inversion of the signal, for a vertically resolved comparison between in situ and remote-sensing results. Note, however, that the comparison was for the most part done in the altitude range where the overlap function is incomplete and accordingly uncertainties are larger. First, the airborne results at low altitudes were validated with the ground measurements. Agreement within approximately ±25 and ±20 % was found for the dry scattering and absorption coefficient, respectively. The single scattering albedo, ranged between 0.83 and 0.95, indicating the importance of the absorbing particles in the Po Valley region. A clear layering of the atmosphere was observed during the beginning of the flight (until ∼  10:00 LT – local time) before the mixing layer (ML) was fully developed. Highest extinction coefficients were found at low altitudes, in the new ML, while values in the residual layer, which could be probed at the beginning of the flight at elevated altitudes, were lower. At the end of the flight (after ∼  12:00 LT) the ML was fully developed, resulting in constant extinction coefficients at all altitudes measured on the Zeppelin NT. Lidar estimates captured these dynamic features well and good agreement was found for the extinction coefficients compared to the in situ results, using fixed lidar ratios (LR) between 30 and 70 sr for the altitudes probed with the Zeppelin. These LR are consistent with values for continental aerosol particles that can be expected in this region.

scholarly journals New In Situ Aerosol Hyperspectral Optical Measurements over 300–700 nm, Part 1: Spectral Aerosol Extinction (SpEx) Instrument Field Validation during the KORUS-OC cruise

2020 ◽  
Author(s):  
Carolyn E. Jordan ◽  
Ryan M. Stauffer ◽  
Brian T. Lamb ◽  
Charles H. Hudgins ◽  
Kenneth L. Thornhill ◽  
...  
Keyword(s):  
Wavelength Range ◽  
Second Order ◽  
Operating Conditions ◽  
Aerosol Size Distribution ◽  
Aerosol Extinction ◽  
Extinction Coefficients ◽  
Characteristic Wavelength ◽  
Order Polynomial ◽  
Visible Wavelengths

Abstract. In situ observations of spectrally-resolved aerosol extinction coefficients (300–700 nm at ~ 0.8 nm resolution) from the May–June 2016 Korea U.S. – Ocean Color (KORUS-OC) oceanographic field campaign are reported. Measurements were made with the custom-built Spectral Aerosol Extinction (SpEx) instrument that previously has been characterized only using laboratory-generated aerosols of known size and composition. Here, the performance of SpEx under realistic operating conditions in the field was assessed by comparison to extinction coefficients derived from commercial instruments that measured scattering and filter-based absorption coefficients at three discrete visible wavelengths. Good agreement was found between these two sets of extinction coefficients with slopes near unity for all 3 wavelengths within the SpEx measurement error (±5 Mm−1). The meteorological conditions encountered during the cruise fostered diverse ambient aerosol populations with varying sizes and composition at concentrations spanning two orders of magnitude. The sampling inlet had a 50 % size cut of 1.3 µm diameter particles such that the in situ aerosol sampling suite deployed aboard ship measured fine mode aerosols only. The extensive hyperspectral extinction data set acquired revealed that nearly all measured spectra exhibited curvature in logarithmic space, such that Ångström exponent (α) power law fits led to large errors compared to measured values, especially in the ultraviolet (UV) wavelength range. This problem was particularly acute for α values calculated over only visible wavelengths, then extrapolated to the UV, highlighting the need for measurements in this wavelength range. Second-order polynomial fits to the logarithmically-transformed data provided a much better fit to the measured spectra than the linear fits of power laws. Building on previous studies that used total column AOD observations to examine the information content of spectral curvature, the relationship between α and the second order polynomial fit coefficients (a1 and a2) was shown to depend on the characteristic wavelength (λch) of any given spectral measurement, such that differing curvature among aerosol size distributions with the same α will map to a line in (a1,a2) space with a slope related to λch. Thus, spectral curvature represented by (a1,a2) may provide more detailed aerosol size distribution information than α alone.

scholarly journals The CU Airborne MAX-DOAS instrument: vertical profiling of aerosol extinction and trace gases

2013 ◽  
Vol 6 (3) ◽  
pp. 719-739 ◽  
Author(s):  
S. Baidar ◽  
H. Oetjen ◽  
S. Coburn ◽  
B. Dix ◽  
I. Ortega ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Spatial Scales ◽  
Trace Gases ◽  
Stray Light ◽  
Aerosol Extinction ◽  
Vertical Profiles ◽  
Maximum Information ◽  
Extinction Coefficients

Abstract. The University of Colorado Airborne Multi-Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (absorption bands at 360, 477, 577, 632 nm) simultaneously in the open atmosphere. The instrument is unique as it (1) features a motion compensation system that decouples the telescope field of view from aircraft movements in real time (<0.35° accuracy), and (2) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system. Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD) below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent. The instrument is described, and data from flights over California during the CalNex (California Research at the Nexus of Air Quality and Climate Change) and CARES (Carbonaceous Aerosols and Radiative Effects Study) air quality field campaigns is presented. Horizontal distributions of NO2 VCD (below the aircraft) maps are sampled with typically 1 km resolution, and show good agreement with two ground-based MAX-DOAS instruments (slope = 0.95 ± 0.09, R2 = 0.86). As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O concentrations and aerosol extinction coefficients, ε, at 477 nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB) are presented. These profiles contain ~12 degrees of freedom (DOF) over a 3.5 km altitude range, an independent information approximately every 250 m. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD) agrees well with nearby ground-based in situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, H2O442, &amp;varepsilon;360, &amp;varepsilon;477 for 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 42 ppm, 0.004 km−1, 0.002 km−1 in the free troposphere (FT), and 30 ppt, 16 ppt, 540 ppt, 252 ppm, 0.012 km−1, 0.006 km−1 inside the boundary layer (BL), respectively. Mobile column observations of trace gases and aerosols are complimentary to in situ observations, and help bridge the spatial scales that are probed by satellites and ground-based observations, and predicted by atmospheric models.

scholarly journals The Spectral Aerosol Extinction Monitoring System (SǼMS): setup, observational products, and comparisons

2014 ◽  
Vol 7 (3) ◽  
pp. 701-712 ◽  
Author(s):  
A. Skupin ◽  
A. Ansmann ◽  
R. Engelmann ◽  
H. Baars ◽  
T. Müller
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Monitoring System ◽  
Aerosol Extinction ◽  
Extinction Coefficients ◽  
Spectrally Resolved ◽  
Automated Instrument ◽  
Statistical Results

Abstract. The Spectral Aerosol Extinction Monitoring System (SǼMS) is presented that allows us to continuously measure the spectral extinction coefficient of atmospheric aerosol particles along an approximately 2.7 km long optical path at 30–50 m height above ground in Leipzig (51.3° N, 12.4° E), Germany. The fully automated instrument measures the ambient aerosol extinction coefficients from 300 to 1000 nm. The main goal of SǼMS observations are long-term studies of the relationship between particle extinction and relative humidity from below 40% to almost 100%. The setup is presented and observations (a case study and statistical results for 2009) are discussed in terms of time series of 550 nm particle optical depth, Ångström exponent, and particle size distribution retrieved from the spectrally resolved extinction. The SǼMS measurements are compared with simultaneously performed EARLINET (European Aerosol Research Lidar Network) lidar, AERONET (Aerosol Robotic Network) sun photometer, and in situ aerosol observations of particle size distribution and related extinction coefficients on the roof of our institute. Consistency between the different measurements is found, which corroborates the quality of the SǼMS observations. Statistical results of a period of 1 yr (2009) show mode extinction values of 0.09 km−1 (SǼMS), 0.075 km−1 (AERONET), and 0.03 km−1 (in situ). Ångström exponents for this period are 0.19 (390–880 nm, SǼMS) and 1.55 (440–870 nm, AERONET).

scholarly journals Diurnal Behavior of Aerosol Optical Properties Studied with Lidar and Ground-Based Instruments

2020 ◽  
Vol 237 ◽  
pp. 02011
Author(s):  
Prane Mariel Ong ◽  
Nofel Lagrosas ◽  
Tatsuo Shiina ◽  
Hiroaki Kuze
Keyword(s):  
Single Scattering ◽  
In Situ Monitoring ◽  
Aerosol Extinction ◽  
Size Change ◽  
Near Surface ◽  
Extinction Coefficients ◽  
Number Distribution ◽  
Combined Use ◽  
Diurnal Behavior

The combined use of remote sensing and in-situ monitoring instruments could help improve the assessment of near-surface aerosol properties. In this paper, we analyze the diurnal behavior of aerosol extinction coefficients, αExt(λ), at λ=349 and 550 nm using a lidar and a present weather detector, respectively. We utilize the aerosol optical thickness (AOT), single scattering albedo (SSA), and Ångström exponent (AE) from SKYNET sky radiometer, and AE from aethalometer, and the number distribution from optical particle counter to evaluate the effect of relative humidity (RH) on aerosol extinction coefficients. It is found that although αExt(λ) often exhibits a positive correlation with the ambient RH, this relation is obscured when both the number distribution and particle size change simultaneously. Moreover, αExt at 349 nm is more sensitive to this change than at 550 nm.

scholarly journals Spectral Aerosol Extinction Monitoring System (SÆMS): setup, observational products, and comparisons

2013 ◽  
Vol 6 (5) ◽  
pp. 8647-8677 ◽  
Author(s):  
A. Skupin ◽  
A. Ansmann ◽  
R. Engelmann ◽  
H. Baars
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Monitoring System ◽  
Aerosol Extinction ◽  
Extinction Coefficients ◽  
Spectrally Resolved ◽  
Automated Instrument

Abstract. A Spectral Aerosol Extinction Monitoring System (SÆMS) is presented that allows us to continuously measure the spectral extinction coefficient of atmospheric aerosol particles along an about 2.7 km long optical path at 30–50 m height above ground at Leipzig (51.3° N, 12.4° E), Germany. The fully automated instrument measures the ambient aerosol extinction coefficients from 300–1000 nm. The main goal of SÆMS observations are long-term studies of the relationship between particle extinction and relative humidity from below 40 % to almost 100 %. The setup is presented and observations (a case study and statistical results for 2009) are discussed in terms of time series of 550 nm particle optical depth, Ångström exponent, and particle size distribution retrieved from the spectrally resolved extinction. The SÆMS measurements are compared with simultaneously performed EARLINET lidar, AERONET photometer, and in situ aerosol observations of particle size distribution and related extinction coefficients at the roof of our institute. Consistency between the different measurements is found which corroborates the quality of the SÆMS observations.

scholarly journals New in situ aerosol hyperspectral optical measurements over 300–700 nm – Part 1: Spectral Aerosol Extinction (SpEx) instrument field validation during the KORUS-OC cruise

2021 ◽  
Vol 14 (1) ◽  
pp. 695-713 ◽  
Author(s):  
Carolyn E. Jordan ◽  
Ryan M. Stauffer ◽  
Brian T. Lamb ◽  
Charles H. Hudgins ◽  
Kenneth L. Thornhill ◽  
...  
Keyword(s):  
Wavelength Range ◽  
Second Order ◽  
Operating Conditions ◽  
Aerosol Extinction ◽  
Size Distributions ◽  
Data Set ◽  
Extinction Coefficients ◽  
Order Polynomial ◽  
Visible Wavelengths

Abstract. In situ observations of spectrally resolved aerosol extinction coefficients (300–700 nm at ∼ 0.8 nm resolution) from the May–June 2016 Korea–United States Ocean Color (KORUS-OC) oceanographic field campaign are reported. Measurements were made with the custom-built Spectral Aerosol Extinction (SpEx) instrument that previously has been characterized only using laboratory-generated aerosols of known size and composition. Here, the performance of SpEx under realistic operating conditions in the field was assessed by comparison to extinction coefficients derived from commercial instruments that measured scattering and filter-based absorption coefficients at three discrete visible wavelengths. Good agreement was found between these two sets of extinction coefficients with slopes near unity for all three wavelengths within the SpEx measurement error (± 5 Mm−1). The meteorological conditions encountered during the cruise fostered diverse ambient aerosol populations with varying sizes and composition at concentrations spanning 2 orders of magnitude. The sampling inlet had a 50 % size cut of 1.3 µm diameter particles such that the in situ aerosol sampling suite deployed aboard ship measured fine-mode aerosols only. The extensive hyperspectral extinction data set acquired revealed that nearly all measured spectra exhibited curvature in logarithmic space, such that Ångström exponent (α) power law fits could lead to large errors compared to measured values. This problem was particularly acute for α values calculated over only visible wavelengths and then extrapolated to the UV, highlighting the need for measurements in this wavelength range. Second-order polynomial fits to the logarithmically transformed data provided a much better fit to the measured spectra than the linear fits of power laws. Building on previous studies that used total column aerosol optical depth observations to examine the information content of spectral curvature, the relationship between α and the second-order polynomial fit coefficients (a1 and a2) was found to depend on the wavelength range of the spectral measurement such that any given α maps into a line in (a1, a2) coefficient space with a slope of −2LN(λch), where λch is defined as the single wavelength that characterizes the wavelength range of the measured spectrum (i.e., the “characteristic wavelength”). Since the curvature coefficient values depend on λch, it must be taken into account when comparing values from spectra obtained from measurement techniques with different λch. Previously published work has shown that different bimodal size distributions of aerosols can exhibit the same α yet have differing spectral curvature with different (a1, a2). This implies that (a1, a2) contain more information about size distributions than α alone. Aerosol size distributions were not measured during KORUS-OC, and the data reported here were limited to the fine fraction, but the (a1, a2) maps obtained from the SpEx data set are consistent with the expectation that (a1, a2) may contain more information than α – a result that will be explored further with future SpEx and size distribution data sets.

scholarly journals The CU Airborne MAX-DOAS instrument: ground based validation, and vertical profiling of aerosol extinction and trace gases

2012 ◽  
Vol 5 (5) ◽  
pp. 7243-7292 ◽  
Author(s):  
S. Baidar ◽  
H. Oetjen ◽  
S. Coburn ◽  
B. Dix ◽  
I. Ortega ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Spatial Scales ◽  
Trace Gases ◽  
Stray Light ◽  
Trace Gas ◽  
Aerosol Extinction ◽  
Vertical Profiles ◽  
Maximum Information ◽  
Extinction Coefficients

Abstract. The University of Colorado Airborne Multi Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light remote sensing to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (360 nm, 477 nm, 577 nm and 632 nm) simultaneously, and sensitively in the open atmosphere. The instrument is unique, in that it presents the first systematic implementation of MAX-DOAS on research aircraft, i.e. (1) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system, and (2) features a motion compensation system that decouples the telescope field of view (FOV) from aircraft movements in real-time (< 0.35° accuracy). Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD) below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent. The instrument is described, and data from flights over California during the CalNex and CARES air quality field campaigns is presented. Horizontal distributions of NO2 VCDs (below the aircraft) maps are sampled with typically 1 km resolution, and show good agreement with two ground based CU MAX-DOAS instruments (slope 0.95 ± 0.09, R2 = 0.86). As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O mixing ratios and aerosol extinction coefficients, ε, at 477nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB) are presented. These profiles contain ~ 12 degrees of freedom (DOF) over a 3.5 km altitude range, independent of signal-to-noise at which the trace gas is detected. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD) agrees well with nearby ground-based in-situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, ε360, ε477 from 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 0.004 km−1, 0.002 km−1 in the free troposphere (FT), and 30 ppt, 16 ppt, 540 ppt, 0.012 km−1, 0.006 km−1 inside the boundary layer (BL), respectively. Mobile column observations of trace gases and aerosols are complimentary to in-situ observations, and help bridge the spatial scales probed by ground-based observations, satellites, and predicted by atmospheric models.

scholarly journals Evaluating model parameterizations of submicron aerosol scattering and absorption with in situ data from ARCTAS 2008

2016 ◽  
Vol 16 (14) ◽  
pp. 9435-9455 ◽  
Author(s):  
Matthew J. Alvarado ◽  
Chantelle R. Lonsdale ◽  
Helen L. Macintyre ◽  
Huisheng Bian ◽  
Mian Chin ◽  
...  
Keyword(s):  
Optical Properties ◽  
Size Distribution ◽  
Aerosol Size Distribution ◽  
Visible Radiation ◽  
Submicron Aerosol ◽  
In Situ Data ◽  
Aerosol Absorption ◽  
Aerosol Scattering ◽  
The Impact

Abstract. Accurate modeling of the scattering and absorption of ultraviolet and visible radiation by aerosols is essential for accurate simulations of atmospheric chemistry and climate. Closure studies using in situ measurements of aerosol scattering and absorption can be used to evaluate and improve models of aerosol optical properties without interference from model errors in aerosol emissions, transport, chemistry, or deposition rates. Here we evaluate the ability of four externally mixed, fixed size distribution parameterizations used in global models to simulate submicron aerosol scattering and absorption at three wavelengths using in situ data gathered during the 2008 Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) campaign. The four models are the NASA Global Modeling Initiative (GMI) Combo model, GEOS-Chem v9-02, the baseline configuration of a version of GEOS-Chem with online radiative transfer calculations (called GC-RT), and the Optical Properties of Aerosol and Clouds (OPAC v3.1) package. We also use the ARCTAS data to perform the first evaluation of the ability of the Aerosol Simulation Program (ASP v2.1) to simulate submicron aerosol scattering and absorption when in situ data on the aerosol size distribution are used, and examine the impact of different mixing rules for black carbon (BC) on the results. We find that the GMI model tends to overestimate submicron scattering and absorption at shorter wavelengths by 10–23 %, and that GMI has smaller absolute mean biases for submicron absorption than OPAC v3.1, GEOS-Chem v9-02, or GC-RT. However, the changes to the density and refractive index of BC in GC-RT improve the simulation of submicron aerosol absorption at all wavelengths relative to GEOS-Chem v9-02. Adding a variable size distribution, as in ASP v2.1, improves model performance for scattering but not for absorption, likely due to the assumption in ASP v2.1 that BC is present at a constant mass fraction throughout the aerosol size distribution. Using a core-shell mixing rule in ASP overestimates aerosol absorption, especially for the fresh biomass burning aerosol measured in ARCTAS-B, suggesting the need for modeling the time-varying mixing states of aerosols in future versions of ASP.

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