Laserfiche WebLink
1 <br /> ti <br /> DRAFT <br /> benzene (0.85 to 2.2 ppb), toluene (0.74 to 4 ppb), ethylbenzene (0.63 ppb), and xylene (0.52 to <br /> i <br /> 4.8 ppb) since 1994 (during 7 of 42 sampling events). Concentrations of TPH-g and benzene in <br /> 1 <br /> groundwater samples from wells peripheral to the former pump island have declined from <br /> relatively high concentrations (3,300 to-110,000 ppb and 160 to 330 ppb respectively) reported <br /> through 1995, to very low concentrations ("non-detect" for TPH=g and 1 ppb to "non-detect" for <br /> benzene) since 1997 (the past nine quarterly monitoring events). Similarly, concentrations of <br /> toluene, ethylbenzene, and xylene in groundwater samples from well MW-2-have historically <br /> ranged from 25,000 to 82,000 ppb, 2,700 to 9,900 ppb, and 14,000 to 37,000 ppb, respectively. <br /> However, concentrations of these constituents are less than MCLs (generally"non detect" to less <br /> than 10 ppb) in groundwater from all other site monitor wells. Thus the data clearly show the <br /> plume is stable, concentrations of residual petroleum hydrocarbons in groundwater are <br /> decreasing, and that residual concentrations in excess of Basin Plan objectives are limited to less <br /> than 60 feet off-site with respectto toluene, ethylbenzene, and xylene, about 70 feet with respect <br /> to benzene, and an estimated 150 feet with regard to TPH-g. <br /> The introduction of petroleum hydrocarbons into the subsurface causes rapid changes in <br /> the,prevailing groundwater geochemistry due to microbially mediated reactions between the <br /> t <br /> hydrocarbons and naturally occurring inorganic compounds. Aerobic respiration, denitrification, <br /> Cp n <br /> Fe (III) reduction, sulfate reduction, and methanogenesis are largely responsible for these st� <br /> changes, and each leaves behind a unique biogeochemical signature. Analyses of the <br /> groundwater samples collected from site wells in March 1998 show that concentrations of <br /> r e{S <br /> educed iron (ferrous) are greater, and.nitrate and sulfate concentrations are significantlyificantl less in e� <br /> l� Y � l <br /> � n WI W yds <br /> samples from wells within the plume when compared to samples from"background"wells. For <br /> example, groundwater samples from up-gradient and cross-gradient wells have ferrous iron <br /> l� <br /> concentrations of less than 0.1 ppm while groundwater samples within the plume have reported 6I 8,q <br /> concentrations ranging from 0.5 to 3.4 ppm. Up-gradient concentrations of nitrate and sulfate are <br /> about 70 ppm and 170 ppm respectively while concentrations of these constituents at the core of <br /> the plume are "non detect" and in down-gradient groundwater nitrate concentrations are "non <br /> detect"while sulfate concentrations are only 10 to 20 ppm. Thus, the data demonstrate that the <br /> dissolved phase hydrocarbon plume in site groundwater is undergoing biodegradation via iron <br /> sulfate and nitrate reduction (i.e.; anaerobic biodegradation). <br /> Measurements of dissolved oxygen in groundwater samples collected from site wells in <br /> February 1999 provide the basis to conclude that aerobic biodegradation is also acting to <br /> I <br /> 1,0 V, s , �� '-f-��- ��►�. n�- <br /> et�_I�� <br /> -�o SIX, � <br />