Drinking water source and exposure to regulated water contaminants in the California Teachers Study cohort.
Pollutants including metals/metalloids, nitrate, disinfection byproducts, and volatile organic compounds contaminate federally regulated community water systems (CWS) and unregulated domestic wells across the United States. Exposures and associated health effects, particularly at levels below regulatory limits, are understudied.
We described drinking water sources and exposures for the California Teachers Study (CTS), a prospective cohort of female California teachers and administrators.
Participants' geocoded addresses at enrollment (1995-1996) were linked to CWS service area boundaries and monitoring data (N = 115,206, 92%); we computed average (1990-2015) concentrations of arsenic, uranium, nitrate, gross alpha (GA), five haloacetic acids (HAA5), total trihalomethanes (TTHM), trichloroethylene (TCE), and tetrachloroethylene (PCE). We used generalized linear regression to estimate geometric mean ratios of CWS exposures across demographic subgroups and neighborhood characteristics. Self-reported drinking water source and consumption at follow-up (2017-2019) were also described.
Medians (interquartile ranges) of average concentrations of all contaminants were below regulatory limits: arsenic: 1.03 (0.54,1.71) µg/L, uranium: 3.48 (1.01,6.18) µg/L, GA: 2.21 (1.32,3.67) pCi/L, nitrate: 0.54 (0.20,1.97) mg/L, HAA5: 8.67 (2.98,14.70) µg/L, and TTHM: 12.86 (4.58,21.95) µg/L. Among those who lived within a CWS boundary and self-reported drinking water information (2017-2019), approximately 74% self-reported their water source as municipal, 15% bottled, 2% private well, 4% other, and 5% did not know/missing. Spatially linked water source was largely consistent with self-reported source at follow-up (2017-2019). Relative to non-Hispanic white participants, average arsenic, uranium, GA, and nitrate concentrations were higher for Black, Hispanic and Native American participants. Relative to participants living in census block groups in the lowest socioeconomic status (SES) quartile, participants in higher SES quartiles had lower arsenic/uranium/GA/nitrate, and higher HAA5/TTHM. Non-metropolitan participants had higher arsenic/uranium/nitrate, and metropolitan participants had higher HAA5/TTHM.
Though average water contaminant levels were mostly below regulatory limits in this large cohort of California women, we observed heterogeneity in exposures across sociodemographic subgroups and neighborhood characteristics. These data will be used to support future assessments of drinking water exposures and disease risk.
Spaur M
，Medgyesi DN
，Bangia K
，Madrigal JM
，Hurwitz LM
，Beane Freeman LE
，Fisher JA
，Spielfogel ES
，Lacey JV Jr
，Sanchez T
，Jones RR
，Ward MH
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Wildfires can increase regulated nitrate, arsenic, and disinfection byproduct violations and concentrations in public drinking water supplies.
Wildfires are a concern for water quality in the United States, particularly in the wildland-urban interface of populous areas. Wildfires combust vegetation and surface soil organic matter, reduce plant nutrient uptake, and can alter the composition of runoff and receiving waters. At the wildland-urban interface, fires can also introduce contaminants from the combustion of man-made structures. We examine post-wildfire effects on drinking water quality by evaluating concentrations and maximum contaminant level (MCL) violations of selected contaminants regulated in the U.S. at public drinking water systems (PWSs) located downstream from wildfire events. Among contaminants regulated under the U.S. Safe Drinking Water Act, nitrate, arsenic, disinfection byproducts, and volatile organic compounds (VOCs) were analyzed in watersheds that experienced major wildfires. Surface water sourced drinking water (SWDW) nitrate violations increased by an average of 0.56 violations per PWS and concentrations increased by 0.044 mg-N/L post-wildfire. Groundwater sourced drinking water (GWDW) nitrate violations increased by 0.069 violations per PWS and concentrations increased by 0.12 mg-N/L post-wildfire. SWDW total trihalomethane (TTHM) violations increased by 0.58 violations per PWS and concentrations increased by 10.4 μg/L. SWDW total haloacetic acid (HAA5) violations increased by 0.82 violations per PWS and concentrations increased by 8.5 μg/L. Arsenic violations increased by 1.08 violations per PWS and concentrations increased by 0.92 μg/L. There was no significant effect of wildfires on average VOC violations. Nitrate violations increased in 75% of SWDW sites and 34% of GWDW sites post-wildfire, while about 71% and 50% of SWDW sites showed an increase in TTHM and HAA5 violations. Violations also increased for 35% of arsenic and 44% of VOC sites post-wildfire. These findings support the need for increased awareness about the impact of wildfires on drinking water treatment to help PWS operators adapt to the consequences of wildfires on source water quality, particularly in wildfire-prone regions.
Pennino MJ
，Leibowitz SG
，Compton JE
，Beyene MT
，LeDuc SD
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