PM2.5 sea salt concentration is estimated as the concentration of chloride ion (Cl-) measured by ion chromatography multiplied by 1.8.  If the chloride measurement is below the detection limit, missing or invalid, and the concentration of chlorine (Cl) measured by XRF is above the detection limit, then the PM2.5 sea salt concentration is estimated as the concentration of chlorine (Cl) measured by XRF multiplied by 1.8. If both chloride and chlorine are missing or invalid, PM2.5 sea salt concentration is not available. Otherwise, PM2.5 sea salt concentration is set to be zero.

A fairly good correlation has been found between PM2.5 and PM10 based on the measurements in 2000-2002 as shown in the figure below. For 2003 and 2004 when PM2.5 mass is missing, PM2.5 is estimated as PM10/1.5, and coarse mass (CM) concentration is then calculated as PM10 - PM2.5.

Figure 1 Relationship between measured PM10 and PM2.5 in 2000-2002

Fine soil concentration = PM2.5 – [Ammonium Sulfate] – [Ammonium Nitrate] – [OMC] – [EC] – [Sea Salt]. If the calculated fine soil is less than zero, it is set to be zero.

Figure 2 Average contributions of major aerosol chemical components to light extinction (Based on data available in 2000-2004)

Figure 3 Average contributions of major aerosol chemical components to light extinction in 20% best, middle 60% and 20% worst days (Based on data available in 2000-2004)

Figure 4 Percentage of sampling days that are 20% worst days in each month (Based on data available in 2000-2004)

 

Figure 5 Average contributions of major aerosol chemical components to light extinction during 20% worst days in each month (Based on data available in 2000-2004)