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Data for Occurrence and Sources of Lead in Private Wells, Sturbridge, Massachusetts

Metadata Updated: July 6, 2024

Lead (Pb) occurrence and sources and aqueous geochemistry were assessed in private wellhead and tap water at a targeted area of concern for possible exceedances and at a control area in the same geologic formation, and in wells at a nearby landfill in south-central Massachusetts (MA). Total Pb concentrations were below the U.S. Environmental Protection Agency (USEPA) Action Level of 15 μg/L in all samples, and about 6% of unfiltered samples contained Pb concentrations that exceeded 1.0 μg/L. Pb concentrations were higher under conditions that are acidic and oxic (pH ≤ 6.5 and dissolved oxygen [DO] ≥ 2 mg/L), in which minerals that could sequester lead or manganese typically are undersaturated, and adsorption by hydrous ferric oxide is limited. Under more neutral to alkaline conditions, the precipitation of Pb in solid solution series minerals such as (Ca,Pb)CO3 and (Ba,Pb)SO4 2, and adsorption by amorphous ferric hydroxides, could limit Pb solubility in the bedrock aquifer or in the plumbing. The low Pb concentrations and the absence of distinctive Pb and strontium (Sr) isotope ratio patterns in samples indicate that a nearby landfill is not likely a significant Pb source. Dissolved concentrations of Pb, copper (Cu), and zinc (Zn) in tap samples were significantly greater than those in wellhead samples, indicating that some Pb is derived from plumbing. Wellhead or tap samples with the highest Pb concentrations also had the greatest corrosivity potential based on the calcite saturation index and the PPGC (Potential to Promote Galvanic Corrosion) and supports the premise that Pb concentrations in tap samples were derived partly from corrosion of plumbing. Concentrations of other constituents, including arsenic (As), uranium (U), Sr, boron (B), and lithium (Li) were not statistically different between the tap and wellhead samples but, apart from Sr, all were statistically higher in the control area than in the target area. This variation in constituent concentrations suggests geochemical variation within the host Paxton Formation, possibly related to faulting and contact with the Ayer granite east of the control area.

Access & Use Information

Public: This dataset is intended for public access and use. License: No license information was provided. If this work was prepared by an officer or employee of the United States government as part of that person's official duties it is considered a U.S. Government Work.

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Dates

Metadata Created Date June 1, 2023
Metadata Updated Date July 6, 2024

Metadata Source

Harvested from DOI EDI

Additional Metadata

Resource Type Dataset
Metadata Created Date June 1, 2023
Metadata Updated Date July 6, 2024
Publisher U.S. Geological Survey
Maintainer
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Identifier USGS:60b6a011d34e86b9388487bc
Data Last Modified 20220222
Category geospatial
Public Access Level public
Bureau Code 010:12
Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID https://datainventory.doi.gov/data.json
Schema Version https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
Harvest Object Id 630d8ec6-b293-48c8-8249-afebd21d712a
Harvest Source Id 52bfcc16-6e15-478f-809a-b1bc76f1aeda
Harvest Source Title DOI EDI
Metadata Type geospatial
Old Spatial -72.067,42.05,-71.93,42.15
Publisher Hierarchy White House > U.S. Department of the Interior > U.S. Geological Survey
Source Datajson Identifier True
Source Hash b29b15dbec2155418af54f87085283ed5df1325924c6f3553d2d54d2c89155ad
Source Schema Version 1.1
Spatial {"type": "Polygon", "coordinates": -72.067, 42.05, -72.067, 42.15, -71.93, 42.15, -71.93, 42.05, -72.067, 42.05}

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