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ARCHIVED REPORTS_XR0004383
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PR0539293
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ARCHIVED REPORTS_XR0004383
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Last modified
11/20/2019 3:28:14 PM
Creation date
11/20/2019 3:20:49 PM
Metadata
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EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0004383
RECORD_ID
PR0539293
PE
2957
FACILITY_ID
FA0022465
FACILITY_NAME
VALLEY MOTORS
STREET_NUMBER
800
Direction
E
STREET_NAME
MAIN
City
STOCKTON
Zip
95202
CURRENT_STATUS
01
SITE_LOCATION
800 E MAIN
P_LOCATION
01
P_DISTRICT
001
QC Status
Approved
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SJGOV\wng
Tags
EHD - Public
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• Nevertheless, VM-2 is downgradient of VM-1 and eastward groundwater flow from VM-1 to <br /> VM-2 would be expected to transport dissolved hydrocarbons to the latter well Concentrations <br /> would thus increase in VM-2 while decreasing in VM-1 (as they have since 1998), but <br /> concentrations in VM-2 could not increase above those that were previously present in VM-1 <br /> However, as Table 2 and Figures 4 and 5 show, concentrations in VM-2 since 1999 far exceed <br /> any that have been detected in VM-I Hence, migration of the dissolved-phase plume could not <br /> be the only process involved <br /> 5.2.2 Hypothesis: Leaching of Hydrocarbons from Soil <br /> A second possibility is that adsorbed hydrocarbons in the vadose zone in the vicinity of VM-2 <br /> have been leached from the soil and carried downward to groundwater Gasoline was detected in <br /> samples at 15 and 20 feet from this boring when it was drilled in 1996, and BTEX compounds <br /> were detected as deep as 35 feet In addition, the area around VM-2 is the only location where <br /> hydrocarbon vapors (up to 970 ppmv) were detected during a soil-vapor survey that was <br /> performed in March 1998 Prior to 1998, the depth to groundwater exceeded 40 feet at the site, <br /> meaning that the gasoline in the 15-20 feet depth interval was separated from groundwater by at <br /> least 20 feet of vadose-zone soil, which could explain why hydrocarbon concentrations remained <br /> constant in the well through 1997 and 1998 (except for August 1998) By the middle of 1998, <br /> groundwater had begun rising rapidly, reaching 33 feet, and may have received a charge of <br /> gasoline if the gasoline had leached downward 10-15 feet during the preceding two years <br /> Leaching could also account for the sharp spike in the TPH-g concentration in VM-1 in early <br /> 1999 Groundwater 4t that time was only 8 feet below the high soil concentration (TPH-g =2,400ti <br /> mg/kg) that was detected at 25 feet when this well was drilled However, this hypothesis cannot <br /> explain why concentrations have continued to rise in VM-2 while declining in VM-1, nor does it <br /> explain why fluctuations in the TPH-g and BTEX concentrations in VM-1 were out of phase <br /> prior to 2001 <br /> 5.2.3 Hypothesis: Leaching Followed by Eastward Plume Migration <br /> A combination of the previous two processes is better able to explain the high concentrations that <br /> have been detected in VM-2 If vadose-zone hydrocarbons near and west of VM-2 leached <br /> downward to groundwater and then migrated toward VM-2, concentrations could rise above <br /> those that have been observed in VM-1 Laboratory data from soil samples that were collected <br /> during the UST removal and from borings (including VM-1) that were drilled later offer some <br /> support to this hypothesis TPH-g concentrations ranged from 3 5 to 27 mg/kg in three of the four <br /> samples that were collected from beneath the UST's during their removal, and five of forty soil <br /> samples that were collected from the soil borings contained hydrocarbons, including one sample <br /> (SB-1-3 at a depth of 14 feet) that contained TPH (reported as Stoddard Solvent) at a <br /> concentration of 183 mg/kg Most BTEX compounds were also detected in these samples (up to <br /> 50 mg/kg xylene in one UST sample and 120 mg/kg xylene in one boring sample) Except for <br /> one boring, these samples were located south of VM-1, making in possible that subsequent <br /> northeastward or eastward migration of the contaminants would be detected in VM-2 but not in <br /> VM-1 <br /> r <br /> 5 <br />
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