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Research about New Hampshire

Source-linked reports with geographic coverage including New Hampshire.

At least 55 records · Page 3Linked to original sources

Concentrations of chloride and sodium in groundwater in New Hampshire from 1960 through 2011

Several studies from the 1970s and more recently (for example, Hall (1975), Daley and others (2009) and Mullaney (2009)) have found that concentrations of chloride and sodium in groundwater in New Hampshire have increased during the past 50 years. Increases likely are related to road salt and other anthropogenic sources, such as septic systems, wastewater, and contamination from landfills and salt-storage areas. According to water-quality data reported to the New Hampshire Department of Environmental Services (NHDES), about 100 public water systems (5 percent) in 2010 had at least one groundwater sample with chloride concentrations that were equal to or exceeded the U.S. Environmental Protection Agency (USEPA) secondary maximum contaminant level (SMCL) of 250 mg/L before the water was treated for public consumption. The SMCL for chloride is a measurement of potential cosmetic or aesthetic effects of chloride in water. High concentrations of chloride and sodium in drinking-water sources can be costly to remove. A new cooperative study between the U.S. Geological Survey (USGS) and the NHDES (Medalie, 2012) assessed chloride and sodium levels in groundwater in New Hampshire from the 1960s through 2011. The purpose of the study was to integrate all data on concentrations of chloride and sodium from groundwater in New Hampshire available from various Federal and State sources, including from the NHDES, the New Hamsphire Department of Health and Human Services, the USGS, and the U.S. Environmental Protection SurveyAgency (USEPA), for public and private (domestic) wells and to organize the data into a database. Medalie (2012) explained the many assumptions and limitations of disparate data that were collected to meet wide-ranging objectives. This fact sheet summarizes the most important findings of the data.

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Bedrock geologic and joint trend map of the Pinardville quadrangle, Hillsborough County, New Hampshire

The bedrock geology of the Pinardville quadrangle includes the Massabesic Gneiss Complex, exposed in the core of a regional northeast-trending anticlinorium, and highly deformed metasedimentary rocks of the Rangeley Formation, exposed along the northwest limb of the anticlinorium. Both formations were subjected to high-grade metamorphism and partial melting: the Rangeley during the middle Paleozoic Acadian orogeny, and the Massabesic Gneiss Complex during both the Acadian and the late Paleozoic Alleghanian orogeny. Granitoids produced during these orogenies range in age from Devonian (Spaulding Tonalite) to Permian (granite at Damon Pond), each with associated pegmatite. In the latest Paleozoic the Massabesic Gneiss Complex was uplifted with respect to the Rangeley Formation along the ductile Powder Hill fault, which also had a left-lateral component. Uplift continued into the early Mesozoic, producing the 2-kilometer-wide Campbell Hill fault zone, which is marked by northwest-dipping normal faults and dilational map-scale quartz bodies. Rare, undeformed Jurassic diabase dikes cut all older lithologies and structures. A second map is a compilation of joint orientations measured at all outcrops in the quadrangle. There is a great diversity of strike trends, with northeast perhaps being the most predominant.

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Characterization of mercury contamination in the Androscoggin River, Coos County, New Hampshire

The former chloralkali facility in Berlin, New Hampshire, was designated a Superfund site in 2005. Historic paper mill activities resulted in the contamination of groundwater, surface water, and sediments with many organic compounds and mercury (Hg). Hg continues to seep into the Androscoggin River in elemental form through bedrock fractures. The objective of this study was to spatially characterize (1) the extent of Hg contamination in water, sediment, and biota; (2) Hg speciation and methylmercury (MeHg) production potential rates in sediment; (3) the availability of inorganic divalent Hg (Hg(II)) for Hg(II)-methylation (MeHg production); and (4) ancillary sediment geochemistry necessary to better understand Hg speciation and MeHg production potential rates in this system. Concentrations of total mercury (THg) and MeHg in sediment, pore water, and biota in the Androscoggin River were elevated downstream from the former chloralkali facility compared with those upstream from reference sites. Sequential extraction of surface sediment showed a distinct difference in Hg speciation upstream compared with downstream from the contamination site. An upstream site was dominated by potassium hydroxide-extractable forms (for example, organic-Hg or particle-bound Hg(II)), whereas sites downstream from the point source were dominated by more chemically recalcitrant forms (largely concentrated nitric acid-extractable), indicative of elemental mercury or mercurous chloride. At all sites, only a minor fraction (less than 0.1 percent) of THg existed in chemically labile forms (for example, water extractable or weak acid extractable). All metrics indicated that a greater percentage of mercury at an upstream site was available for Hg(II)-methylation compared with sites downstream from the point source, but the absolute concentration of bioavailable Hg(II) was greater downstream from the point source. In addition, the concentration of tin-reducible inorganic reactive mercury, a surrogate measure of bioavailable Hg(II) generally increased with distance downstream from the point source. Whereas concentrations of mercury species on a sediment-dry-weight basis generally reflected the relative location of the sample to the point source, river-reach integrated mercury-species inventories and MeHg production potential (MPP) rates reflected the amount of fine-grained sediment in a given reach. THg concentrations in biota were significantly higher downstream from the point source compared with upstream reference sites for smallmouth bass, white sucker, crayfish, oligochaetes, bat fur, nestling tree swallow blood and feathers, adult tree swallow blood, and tree swallow eggs. As with tin-reducible inorganic reactive mercury, THg in smallmouth bass also increased with distance downstream from the point source. Toxicity tests and invertebrate community assessments suggested that invertebrates were not impaired at the current (2009 and 2010) levels of mercury contamination downstream from the point source. Concentrations of THg and MeHg in most water and sediment samples from the Androscoggin River were below U.S. Environmental Protection Agency (USEPA), the Canadian Council of Ministers of the Environment, and probable effects level guidelines. Surface-water and sediment samples from the Androscoggin River had similar THg concentrations but lower MeHg concentrations compared with other rivers in the region. Concentrations of THg in fish tissue were all above regional and U.S. Environmental Protection Agency guidelines. Moreover, median THg concentrations in smallmouth bass from the Androscoggin River were significantly higher than those reported in regional surveys of river and streams nationwide and in the Northeastern United States and Canada. The higher concentrations of mercury in smallmouth bass suggest conditions may be more favorable for Hg(II)-methylation and bioaccumulation in the Androscoggin River compared with many other rivers in the United States and Canada.

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Physical, chemical, and isotopic data from groundwater in the watershed of Mirror Lake, and in the vicinity of Hubbard Brook, near West Thornton, New Hampshire, 1983 to 1997

Research on the hydrogeologic setting of Mirror Lake near West Thornton, New Hampshire (43° 56.5’ N, 71° 41.5’ W), includes the study of the physical, chemical, and isotopic characteristics of groundwater in the vicinity of the lake and nearby Hubbard Brook. Presented here are those physical, chemical, and isotopic data for the period 1983 to 1997. Data were collected from observation wells installed in glacial drift and bedrock, as well as from one domestic well in the general area of the lake and Hubbard Brook. Also presented are data for Mirror Lake for August 1, 1993, to place groundwater data in context with chemical and isotopic characteristics of the lake.

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Geochemical, isotopic, and dissolved gas characteristics of groundwater in a fractured crystalline-rock aquifer, Savage Municipal Well Superfund site, Milford, New Hampshire, 2011

Tetrachloroethylene (PCE), a volatile organic compound, was detected in groundwater from deep (more than (>) 300 feet (ft) below land surface) fractures in monitoring wells tapping a crystalline-rock aquifer beneath operable unit 1 (OU1) of the Savage Municipal Well Superfund site (Weston, Inc., 2010). Operable units define remedial areas of contaminant concern. PCE contamination within the fractured-rock aquifer has been designated as a separate operable unit, operable unit 3 (OU3; Weston, Inc., 2010). PCE contamination was previously detected in the overlying glacial sand and gravel deposits and basal till, hereafter termed the Milford-Souhegan glacial-drift (MSGD) aquifer (Harte, 2004, 2006). Operable units 1 and 2 encompass areas within the MSGD aquifer, whereas the extent of the underlying OU3 has yet to be defined. The primary original source of contamination has been identified as a former manufacturing facility—the OK Tool manufacturing facility; hence OU1 sometimes has been referred to as the OK Tool Source Area (New Hampshire Department of Environmental Services, undated). A residential neighborhood of 30 to 40 houses is located in close proximity (one-quarter of a mile) from the PCE-contaminated monitoring wells. Each house has its own water-supply well installed in similar rocks as those of the monitoring wells, as indicated by the New Hampshire State geologic map (Lyons and others, 1997). An investigation was initiated in 2010 by the U.S. Environmental Protection Agency (USEPA) region 1, and the New Hampshire Department of Environmental Services (NHDES) to assess the potential for PCE transport from known contaminant locations (monitoring wells) to the residential wells. The U.S. Geological Survey (USGS) and the NHDES entered into a cooperative agreement in 2011 to assist in the evaluation of PCE transport in the fractured-rock aquifer. Periodic sampling over the last decade by the USEPA and NHDES has yet to detect PCE in groundwater from the residential-supply wells (as of 2012). However, part of assessing the potential for PCE transport involves understanding the origin of the groundwater in the monitoring and residential wells. One of the tools in delineating the movement of groundwater to wells, particularly in complex, highly heterogeneous fractured-rock aquifers, is the understanding of the geochemical and isotopic composition of groundwater (Lipfert and Reeve, 2004; Harte and others, 2012). This report summarizes findings from analyses of geochemical, isotopic, and dissolved gas characteristics of groundwater. Samples of groundwater were collected in 2011 from monitoring wells and nearby residential-supply wells in proximity to OU1.

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Bedrock geology and outcrop fracture trends in the vicinity of the Savage Municipal Well Superfund site, Milford, New Hampshire

The Savage Municipal Well Superfund site consists of an eastward-directed plume of volatile organic compounds, principally tetrachloroethylene (PCE), in alluvium and glacial sand and gravel in the Souhegan River valley, just south of the river and about 4 kilometers west of the town of Milford, New Hampshire. Sampling of monitoring wells at the site has helped delineate the extent of the plume and has determined that some contaminant has migrated into the underlying crystalline bedrock, including bedrock north of the river within 200 meters of a nearby residential development that was constructed in 1999. Borehole geophysical logging has identified a northeast preferential trend for bedrock fractures, which may provide a pathway for the migration of contaminant under and north of the Souhegan River. The current study investigates the bedrock geologic setting for the site, including its position relative to known regional geologic structures, and compiles new strike and dip measurements of joints in exposed bedrock to determine if there are dominant trends in orientation similar to what was found in the boreholes. The site is located on the northwestern limb of a northeast-trending regional anticlinorium that is southeast of the Campbell Hill fault zone. The Campbell Hill fault zone defines the contact between granite and gneiss of the anticlinorium and granite and schist to the northwest and is locally marked by lenses of massive vein quartz, minor faults, and fracture zones that could potentially affect plume migration. The fault zone was apparently not intercepted by any of the boreholes that were drilled to delineate the contaminant plume and therefore passes to the north of the northernmost borehole in the vicinity of the new residential area. Joints measured in surface exposures indicate a strong preferred direction of strike to the north-northeast corroborating the borehole data and previous outcrop and geophysical studies. The north-northeast preferred direction matches the direction of elongation of the cone of depression formed during a pump test of the bedrock wells and could explain a potential pathway for the migration of contaminant north of the river.

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Hydrogeologic framework, arsenic distribution, and groundwater geochemistry of the glacial-sediment aquifer at the Auburn Road landfill superfund site, Londonderry, New Hampshire

Leachate continues to be generated from landfills at the Auburn Road Landfill Superfund Site in Londonderry, New Hampshire. Impermeable caps on the three landfills at the site inhibit direct infiltration of precipitation; however, high water-table conditions allow groundwater to interact with landfill materials from below, creating leachate and ultimately reducing conditions in downgradient groundwater. Reducing conditions can facilitate arsenic transport by allowing it to stay in solution or by liberating arsenic adsorbed to surfaces and from geologic sources, such as glacial sediments and bedrock. The site occupies a 180-acre parcel of land containing streams, ponds, wetlands, and former gravel pits located in glacial sediment. Four areas, totaling 14 acres, including three landfills and one septage lagoon, were used for waste disposal. The site was closed in 1980 after volatile organic compounds associated with industrial waste dumping were detected. The site was added to the U.S. Environmental Protection Agency National Priority List in 1982, and the landfills were capped in 1996. Although volatile organic compound concentrations in groundwater have declined substantially, some measurable concentrations remain. Temporally variable and persistent elevated arsenic concentrations have been measured in groundwater affected by the landfill leachate. Microbial consumption of carbon found in leachate is a driver of reducing conditions that liberate arsenic at the site. In addition to sources of carbon in landfill leachate, wetland areas throughout the site also could contribute carbon to groundwater, but it is currently unknown if any of the wetland areas have downward or reversing gradients that could allow the infiltration of surface water to groundwater. Red-stained sediments and water indicate iron-rich groundwater discharge to surface water and are also associated with elevated concentrations of arsenic in sediment and groundwater. Ironrich groundwater seeps have been observed in the wetland, streams, and pond downgradient of the landfills. Piezometers were installed in some of these locations to confirm groundwater discharge, measure vertical-flow gradients, and to provide a way to sample the discharging groundwater. Understanding the movement of leachate in groundwater is complicated by the presence of preferential flow paths through aquifer materials with differing hydraulic properties; these preferential flow paths can affect rates of recharge, geochemical conditions, and contaminant fluxes. In areas adjacent to the three capped landfills, infiltration of precipitation containing oxygenated water through permeable deltaic sediments in the former gravel pit area causes increases in dissolved oxygen concentrations and decreases in arsenic concentrations. Layered deltaic sediments produce anisotropic hydraulic characteristics and zones of high hydraulic conductivity. The glacial-sediment aquifer also includes glaciolacustrine sediments that have low permeability and limit infiltration at the surface Discharge of leachate-affected groundwater may be limited in areas of organic muck on the bottom of Whispering Pines Pond because the muck may act as a semiconfining layer. Geophysical survey results were used to identify several areas with continuous beds of muck and an underlying highresistivity layer on top of a layer of low resistivity that may represent leachate-affected groundwater. The high-resistivity layer is likely groundwater associated with oxygenated recharge, which would cause arsenic to adsorb onto aquifer sediments and reduce concentrations of dissolved arsenic in groundwater. Surface and borehole geophysical data collected in 2011 were used to identify potentially high-permeability or contaminated zones in the aquifer (preferential flowpaths) as well as low-permeability zones that may promote contamination through back diffusion. Some groundwater in parts of the glacial-sediment aquifer where the leachate plumes were present had low electrical resistivity, low dissolved oxygen, and high concentrations of arsenic. Low-resistivity zones in the underlying bedrock were associated with fractures that also may contain leachate. Although surveying the fractured bedrock was not a specific objective of this study, the results suggest that such a survey would help to determine if leachate and associated concentrations of arsenic are migrating downward into the fractured-bedrock-aquifer system. An uncalibrated, one-dimensional, reactive-transport model was used to assess several conditions that affect arsenic mobility. The results indicate that reductive dissolution and desorption from glacial sediments control dissolved arsenic concentrations. Parameter sensitivity analysis was used to identify key data that are needed in order to accurately assess the time required for arsenic concentrations to fall to levels below the maximum contaminant level at the site. Quantifying this time will require accurate characterization of carbon, sediment-surface sorption sites, and groundwater fluxes at the site.

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Fracture characterization by means of attenuation and generation of tube waves in fractured crystalline rock at Mirror Lake, New Hampshire

Results are presented from experiments carried out in conjunction with the U. S. Geological Survey at the Hubbard Brook Experimental Forest near Mirror Lake, New Hampshire. The study focuses on our ability to obtain orientation and transmissivity estimates of naturally occurring fractures. The collected data set includes a four-offset hydrophone vertical seismic profile, full waveform acoustic logs at 5, 15, and 34 kHz, borehole televiewer, temperature, resistivity, and self-potential logs, and borehole-to-borehole pump test data. Borehole televiewer and other geophysical logs indicate that permeable fractures intersect the Mirror Lake boreholes at numerous depths, but less than half of these fractures appear to have significant permeability beyond the annulus of drilling disturbance on the basis of acoustic waveform log analysis. The vertical seismic profiling (VSP) data indicate a single major permeable fracture near a depth of 44 m, corresponding to one of the most permeable fractures identified in the acoustic waveform log analysis. VSP data also indicate a somewhat less permeable fracture at 220 m and possible fractures at depths of 103 and 135 m; all correspond to major permeable fractures in the acoustic waveform data set. Pump test data confirm the presence of a hydraulic connection between the Mirror Lake boreholes through a shallow dipping zone of permeability at 44 m in depth. Effective fracture apertures calculated from modeled transmissivities correspond to those estimated for the largest fractures indicated on acoustic waveform logs but are over an order of magnitude larger than effective apertures calculated from tube waves in the VSP data set. This discrepancy is attributed to the effect of fracture stiffness. A new model is presented to account for the mechanical strength of asperities in resisting fracture closure during the passage of seismic waves during the generation of VSPs.

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Heterogeneous redox conditions, arsenic mobility, and groundwater flow in a fractured-rock aquifer near a waste repository site in New Hampshire, USA

Anthropogenic sources of carbon from landfill or waste leachate can promote reductive dissolution of in situ arsenic (As) and enhance the mobility of As in groundwater. Groundwater from residential-supply wells in a fractured crystalline-rock aquifer adjacent to a Superfund site in Raymond, New Hampshire, USA, showed evidence of locally enhanced As mobilization in relatively reducing (mixed oxic-anoxic to anoxic) conditions as determined by redox classification and other lines of evidence. Redox classification was determined from geochemical indicators based on threshold concentrations of dissolved oxygen (DO), nitrate (NO 3- ), iron (Fe 2+ ), manganese (Mn 2+ ), and sulfate (SO 4 2- ). Redox conditions were evaluated also based on methane (CH 4 ), excess nitrogen gas (N 2 ) from denitrification, the oxidation state of dissolved As speciation (As(III) and As(V)), and several stable isotope ratios. Samples from the residential-supply wells primarily exhibit mixed redox conditions, as most have long open boreholes (typically 50–100 m) that receive water from multiple discrete fractures with contrasting groundwater chemistry and redox conditions. The methods employed in this study can be used at other sites to gauge redox conditions and the potential for As mobilization in complex fractured crystalline-rock aquifers where multiple lines of evidence are likely needed to understand As occurrence, mobility, and transport.

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Time series geophysical monitoring of permanganate injections and in situ chemical oxidation of PCE, OU1 area, Savage Superfund Site, Milford, NH, USA

In situ chemical oxidation (ISCO) treatment with sodium permanganate, an electrically conductive oxidant, provides a strong electrical signal for tracking of injectate transport using time series geophysical surveys including direct current (DC) resistivity and electromagnetic (EM) methods. Effective remediation is dependent upon placing the oxidant in close contact with the contaminated aquifer. Therefore, monitoring tools that provide enhanced tracking capability of the injectate offer considerable benefit to guide subsequent ISCO injections. Time-series geophysical surveys were performed at a superfund site in New Hampshire, USA over a one-year period to identify temporal changes in the bulk electrical conductivity of a tetrachloroethylene (PCE; also called tetrachloroethene) contaminated, glacially deposited aquifer due to the injection of sodium permanganate. The ISCO treatment involved a series of pulse injections of sodium permanganate from multiple injection wells within a contained area of the aquifer. After the initial injection, the permanganate was allowed to disperse under ambient groundwater velocities. Time series geophysical surveys identified the downward sinking and pooling of the sodium permanganate atop of the underlying till or bedrock surface caused by density-driven flow, and the limited horizontal spread of the sodium permanganate in the shallow parts of the aquifer during this injection period. When coupled with conventional monitoring, the surveys allowed for an assessment of ISCO treatment effectiveness in targeting the PCE plume and helped target areas for subsequent treatment.

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Temperature logging of groundwater in bedrock wells for geothermal gradient characterization in New Hampshire, 2012

The U.S. Geological Survey, in cooperation with the New Hampshire Geological Survey, measured the fluid temperature of groundwater in deep bedrock wells in the State of New Hampshire in order to characterize geothermal gradients in bedrock. All wells selected for the study had low water yields, which correspond to low groundwater flow from fractures. This reduced the potential for flow-induced temperature changes that would mask the natural geothermal gradient in the bedrock. All the wells included in this study were privately owned, and permission to use the wells was obtained from homeowners before logging. Maximum groundwater temperatures at the bottom of the logs were between 11.7 and 17.3 degrees Celsius. Geothermal gradients were generally higher than typically reported for other water wells in the United States. Some of the high gradients were associated with high natural gamma emissions. Groundwater flow was discernible in 5 of the 10 wells studied but only obscured the portion of the geothermal gradient signal where groundwater actually flowed through the well. Temperature gradients varied by mapped bedrock type but can also vary by differences in mineralogy or rock type within the wells.

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Evaluation of modeling for groundwater flow and tetrachloroethylene transport in the Milford-Souhegan glacial-drift aquifer at the Savage Municipal Well Superfund site, Milford, New Hampshire, 2011

The U.S. Geological Survey and the New Hampshire Department of Environmental Services entered into a cooperative agreement to assist in the evaluation of remedy simulations of the MSGD aquifer that are being performed by various parties to track the remedial progress of the PCE plume. This report summarizes findings from this evaluation. Topics covered include description of groundwater flow and transport models used in the study of the Savage Superfund site (section 2), evaluation of models and their results (section 3), testing of several new simulations (section 4), an assessment of the representation of models to simulate field conditions (section 5), and an assessment of models as a tool in remedial operational decision making (section 6).

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Temporal and spatial trends of chloride and sodium in groundwater in New Hampshire, 1960–2011

Data on concentrations of chloride and sodium in groundwater in New Hampshire were assembled from various State and Federal agencies and organized into a database. This report provides documentation of many assumptions and limitations of disparate data that were collected to meet wide-ranging objectives and investigates temporal and spatial trends of the data. Data summaries presented in this report and analyses performed for this study needed to take into account the 27 percent of chloride and 5 percent of sodium data that were censored (less than a reporting limit) at multiple reporting limits that systematically decreased over time. Throughout New Hampshire, median concentrations of chloride were significantly greater during 2000-2011 than in every decade since the 1970s, and median concentrations of sodium were significantly greater during 2000-2011 than during the 1990s. Results of summary statistics showed that the 50th, 75th, and 90th percentiles of the median concentrations of chloride and sodium by source (well) from Rockingham and Strafford counties were the highest in the State; and the 75th and 90th percentiles from Carroll, Coos, and Grafton counties were the lowest. Large increases in median concentrations of chloride and sodium for individual wells after 1995 compared with concentrations for years before were found in parts of Belknap and Rockingham counties and in small clusters within Carroll, Hillsborough, and Merrimack counties.

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Flood-inundation maps for the Suncook River in Epsom, Pembroke, Allenstown, and Chichester, New Hampshire

Digital flood-inundation maps for a 16.5-mile reach of the Suncook River in Epsom, Pembroke, Allenstown, and Chichester, N.H., from the confluence with the Merrimack River to U.S. Geological Survey (USGS) Suncook River streamgage 01089500 at Depot Road in North Chichester, N.H., were created by the USGS in cooperation with the New Hampshire Department of Homeland Security and Emergency Management. The inundation maps presented in this report depict estimates of the areal extent and depth of flooding corresponding to selected water levels (stages) at the USGS streamgage at Suncook River at North Chichester, N.H. (station 01089500). The current conditions at the USGS streamgage may be obtained on the Internet (http://waterdata.usgs.gov/nh/nwis/uv/?site_no=01089500&PARAmeter_cd=00065,00060). The National Weather Service forecasts flood hydrographs at many places that are often collocated with USGS streamgages. Forecasted peak-stage information is available on the Internet at the National Weather Service (NWS) Advanced Hydrologic Prediction Service (AHPS) flood-warning system site (http://water.weather.gov/ahps/) and may be used in conjunction with the maps developed in this study to show predicted areas of flood inundation. These maps along with real-time stream stage data from the USGS Suncook River streamgage (station 01089500) and forecasted stream stage from the NWS will provide emergency management personnel and residents with information that is critical for flood-response activities, such as evacuations, road closures, disaster declarations, and post-flood recovery. The maps, along with current stream-stage data from the USGS Suncook River streamgage and forecasted stream-stage data from the NWS, can be accessed at the USGS Flood Inundation Mapping Science Web site http://water.usgs.gov/osw/flood_inundation/.

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Estimated probability of arsenic in groundwater from bedrock aquifers in New Hampshire, 2011

Probabilities of arsenic occurrence in groundwater from bedrock aquifers at concentrations of 1, 5, and 10 micrograms per liter (µg/L) were estimated during 2011 using multivariate logistic regression. These estimates were developed for use by the New Hampshire Environmental Public Health Tracking Program. About 39 percent of New Hampshire bedrock groundwater was identified as having at least a 50 percent chance of containing an arsenic concentration greater than or equal to 1 µg/L. This compares to about 7 percent of New Hampshire bedrock groundwater having at least a 50 percent chance of containing an arsenic concentration equaling or exceeding 5 µg/L and about 5 percent of the State having at least a 50 percent chance for its bedrock groundwater to contain concentrations at or above 10 µg/L. The southeastern counties of Merrimack, Strafford, Hillsborough, and Rockingham have the greatest potential for having arsenic concentrations above 5 and 10 µg/L in bedrock groundwater. Significant predictors of arsenic in groundwater from bedrock aquifers for all three thresholds analyzed included geologic, geochemical, land use, hydrologic, topographic, and demographic factors. Among the three thresholds evaluated, there were some differences in explanatory variables, but many variables were the same. More than 250 individual predictor variables were assembled for this study and tested as potential predictor variables for the models. More than 1,700 individual measurements of arsenic concentration from a combination of public and private water-supply wells served as the dependent (or predicted) variable in the models. The statewide maps generated by the probability models are not designed to predict arsenic concentration in any single well, but they are expected to provide useful information in areas of the State that currently contain little to no data on arsenic concentration. They also may aid in resource decision making, in determining potential risk for private wells, and in ecological-level analysis of disease outcomes. The approach for modeling arsenic in groundwater could also be applied to other environmental contaminants that have potential implications for human health, such as uranium, radon, fluoride, manganese, volatile organic compounds, nitrate, and bacteria.

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A transect through the base of the Bronson Hill Terrane in western New Hampshire

This trip will present the preliminary results of ongoing bedrock mapping in the North Hartland and Claremont North 7.5-minute quadrangles in western New Hampshire. The trip will travel from the Lebanon pluton to just north of the Sugar River pluton (Fig. 1) with the aim of examining the lower structural levels of the Bronson Hill anticlinorium (BHA), and the nature of the boundary with the rocks of the Connecticut Valley trough (CVT). Spear and others (2002, 2003, 2008) proposed that western New Hampshire was characterized by five major faults bounding five structural levels including, from lowest to highest, the “chicken yard line”, Western New Hampshire Boundary Thrust, Skitchewaug nappe, Fall Mountain nappe, and Chesham Pond nappe. Lyons and others (1996, 1997) showed the lowest level cored by the Cornish nappe and floored by the Monroe fault. Thompson and others (1968) explained the geometry of units by folding without major thrust faults, and described the second level as the Skitchewaug nappe. This trip will focus on the two lowest levels which we have revised to call the Monroe and Skitchewaug Mountain thrust sheets. Despite decades of geologic mapping in the northeastern United States at various scales, little 1:24,000-scale (or larger scale) modern bedrock mapping has been published for the state of New Hampshire. In fact, of the New England states, New Hampshire contains the fewest published, modern bedrock geologic maps. Conversely, adjacent Vermont has a relatively high percentage of modern bedrock maps due to focused efforts to create a new state-wide bedrock geologic map over the last few decades. The new Vermont map (Ratcliffe and others, 2011) has identified considerable gaps in our knowledge of the bedrock geology in adjacent New Hampshire where published maps are, in places, more than 50 years old and at scales ranging from 1:62,500 to 1:250,000. Fundamental questions remain concerning the geology across the Connecticut River, especially in regards to the stratigraphy of the BHA and CVT, and the distribution, or even existence, of faults ranging in age from Devonian to Mesozoic (e.g., Spear and others, 2008; McWilliams and others, 2010; Walsh and others, 2010). Questions to ponder on this trip include, but are not limited to: 1) Is the Bronson Hill anticlinorium allochthonous? 2) What is the crust beneath the Bronson Hill anticlinorium? 3) Is there a “Big Staurolite nappe” as proposed by Spear and others (2002, 2003, 2008)? 4) What is the role of Taconic, Acadian, and Alleghanian orogenesis in the tectonic development of the region? Modern 1:24,000-scale mapping is the first step towards answering these questions. Mapping will be supplemented by modern geochronology and geochemistry as this project develops. We plan to share some of our provisional results during this field trip.

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Changes in monoterpene mixing ratios during summer storms in rural New Hampshire (USA)

Monoterpenes are an important class of biogenic hydrocarbons that influence ambient air quality and are a principle source of secondary organic aerosol (SOA). Emitted from vegetation, monoterpenes are a product of photosynthesis and act as a response to a variety of environmental factors. Most parameterizations of monoterpene emissions are based on clear weather models that do not take into account episodic conditions that can drastically change production and release rates into the atmosphere. Here, the monoterpene dataset from the rural Thompson Farm measurement site in Durham, New Hampshire is examined in the context of a set of known severe storm events. While some storm systems had a negligible influence on ambient monoterpene mixing ratios, the average storm event increased mixing ratios by 0.59 ± 0.21 ppbv, a factor of 93% above pre-storm levels. In some events, mixing ratios reached the 10's of ppbv range and persisted overnight. These mixing ratios correspond to increases in the monoterpene emission rate, ranging from 120 to 1240 g km −2 h −1 compared to an estimated clear weather rate of 116 to 193 g km −2 h −1 . Considering the regularity of storm events over most forested areas, this could be an important factor to consider when modeling global monoterpene emissions and their resulting influence on the formation of organic aerosols.

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Inference about density and temporary emigration in unmarked populations

Few species are distributed uniformly in space, and populations of mobile organisms are rarely closed with respect to movement, yet many models of density rely upon these assumptions. We present a hierarchical model allowing inference about the density of unmarked populations subject to temporary emigration and imperfect detection. The model can be fit to data collected using a variety of standard survey methods such as repeated point counts in which removal sampling, double‐observer sampling, or distance sampling is used during each count. Simulation studies demonstrated that parameter estimators are unbiased when temporary emigration is either “completely random” or is determined by the size and location of home ranges relative to survey points. We also applied the model to repeated removal sampling data collected on Chestnut‐sided Warblers ( Dendroica pensylvancia ) in the White Mountain National Forest, USA. The density estimate from our model, 1.09 birds/ha, was similar to an estimate of 1.11 birds/ha produced by an intensive spot‐mapping effort. Our model is also applicable when processes other than temporary emigration affect the probability of being available for detection, such as in studies using cue counts. Functions to implement the model have been added to the R package unmarked .

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