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Determination of δ13C, δ15N, or δ34S by isotope-ratio-monitoring mass spectrometry using an elemental analyzer

This report describes procedures used in the Geology, Geophysics, and Geochemistry Science Center of the U.S. Geological Survey in Denver, Colorado, to determine the stable-isotope ratios 13 C/ 12 C, 15 N/ 14 N, and 34 S/ 32 S in solid materials. The procedures use elemental analyzers connected directly to gas-source isotope-ratio mass spectrometers. A different elemental–analyzer–mass-spectrometer system is used for 13 C/ 12 C and 15 N/ 14 N than is used for 34 S/ 32 S to accommodate differences in reagents, catalysts, and instrument settings.

Techniques and Methods

A modular finite-element model (MODFE) for areal and axisymmetric ground-water-flow problems, Part 3: Design philosophy and programming details

A MODular Finite-Element, digital-computer program (MODFE) was developed to simulate steady or unsteady-state, two-dimensional or axisymmetric ground-water-flow. The modular structure of MODFE places the computationally independent tasks that are performed routinely by digital-computer programs simulating ground-water flow into separate subroutines, which are executed from the main program by control statements. Each subroutine consists of complete sets of computations, or modules, which are identified by comment statements, and can be modified by the user without affecting unrelated computations elsewhere in the program. Simulation capabilities can be added or modified by either adding or modifying subroutines that perform specific computational tasks, and the modular-program structure allows the user to create versions of MODFE that contain only the simulation capabilities that pertain to the ground-water problem of interest. MODFE is written in a Fortran programming language that makes it virtually device independent and compatible with desk-top personal computers and large mainframes. MODFE uses computer storage and execution time efficiently by taking advantage of symmetry and sparseness within the coefficient matrices of the finite-element equations. Parts of the matrix coefficients are computed and stored as single-subscripted variables, which are assembled into a complete coefficient just prior to solution. Computer storage is reused during simulation to decrease storage requirements. Descriptions of subroutines that execute the computational steps of the modular-program structure are given in tables that cross reference the subroutines with particular versions of MODFE. Programming details of linear and nonlinear hydrologic terms are provided. Structure diagrams for the main programs show the order in which subroutines are executed for each version and illustrate some of the linear and nonlinear versions of MODFE that are possible. Computational aspects of changing stresses and boundary conditions with time and of mass-balance and error terms are given for each hydrologic feature. Program variables are listed and defined according to their occurrence in the main programs and in subroutines. Listings of the main programs and subroutines are given.

Techniques of Water-Resources Investigations

Organic compounds and trace elements in fish tissue and bed sediment from streams in the Yellowstone River basin, Montana and Wyoming, 1998

A comprehensive water-quality investigation of the Yellowstone River Basin began in 1997, under the National Water-Quality Assessment (NAWQA) Program. Twenty-four sampling sites were selected for sampling of fish tissue and bed sediment during 1998. Organic compounds analyzed included organochlorine insecticides and their metabolites and total polychlorinated biphenyls (PCBs) from fish-tissue and bed-sediment samples, and semivolatile organic compounds from bed-sediment samples. A broad suite of trace elements was analyzed from both fish-tissue and bed-sediment samples, and a special study related to mercury also was conducted. Of the 12 organochlorine insecticides and metabolites detected in the fish-tissue samples, the most compounds per site were detected in samples from integrator sites which represent a mixture of land uses. The presence of DDT, and its metabolites DDD and DDE, in fish collected in the Yellowstone Park area likely reflects long-term residual effects from historical DDT-spraying programs for spruce budworm. Dieldrin, chlordane, and other organic compounds also were detected in the fish-tissue samples. The compound p, p'-DDE was detected at 71 percent of the sampling sites, more than any other compound. The concentrations of total DDT in fish samples were low, however, compared to concentrations from historical data from the study area, other NAWQA studies in the Rocky Mountains, and national baseline concentrations. Only 2 of the 27 organochlorine insecticides and metabolites and total PCBs analyzed in bed sediment were detected. Given that 12 of the compounds were detected in fish-tissue samples, fish appeared to be more sensitive indicators of contamination than bed sediment.Concentrations of some trace elements in fish and bed sediment were higher at sites in mineralized areas than at other sites. Concentrations of selenium in fish tissue from some sites were above background levels. Concentrations of arsenic, chromium, copper, and lead in some of the bed-sediment samples potentially exceeded criteria for the protection of aquatic life.

Water-Resources Investigations Report

Selected elements and organic chemicals in streambed sediment in the Salem area, Oregon, 1999

Analysis of streambed sediments in the Salem, Oregon, area showed anomalously large concentrations of some elements and organic chemicals, indicating contamination from anthropogenic and/or geologic sources. The streambed sediment sample from Clark Creek, an urban basin, had large concentrations of polycyclic aromatic hyrdocarbons (PAHs), organochlorines, cadmium, lead, and zinc. The sample from the East Fork of Pringle Creek, which is a mostly urban basin, had the highest concentrations of DDD, DDE, and DDT compounds. Aldrin was detected in streambed sediment at only one site, the East Fork of Pringle Creek. Ten of the 14 sites sampled had exceedances of the sediment quality guidelines of the Canadian Council of Ministers of the Environment (CCME), and 8 sites had exceedances of guidelines from the Puget Sound Dredged Disposal Analysis (PSDDA) Program. Trace element concentrations in the Salem area generally were similar to those found previously in the Willamette Basin and nationally. However, cadmium, lead, and zinc concentrations were larger in the sample from Clark Creek than for largest value for Willamette Basin data from earlier studies. Zinc concentrations in the sample from Clark Creek exceeded sediment quality guidelines from the CCME and PSDDA. p,p'-DDE, which is a persistent breakdown product of the banned organochlorine-insecticide, DDT, was detected at all sites. Total DDT (the sum of p,p'-DDD, p,p'-DDE, and p,p'-DDT) concentrations exceeded the PSDDA screening level at eight sites and exceeded twice the PSDDA maximum level at the East Fork of Pringle Creek. Cis- and trans- chlordanes were detected at about 80% of the sites. The concentration of total chlordane for the sample at Clark Creek was larger than for any sample from previous Willamette Basin studies. The largest concentration of dieldrin also was from the sample at Clark Creek, which was the only site that exceeded the CCME guideline for dieldrin. The high levels of contaminants in some Salem area streams indicates the need for further study to assess the biological effects of these contaminants. Future monitoring in the Salem area could include bioassays using benthic invertebrates and the measurement of organochlorine compounds, including DDT, DDE, DDD, and dieldrin in fish tissue. Because resident fish may be consumed by humans and wildlife, fish tissue analyses would be helpful to determine the health risk associated with fish consumption.

Water-Resources Investigations Report

Hypolimnetic concentrations of dissolved oxygen, nutrients, and trace elements in Coeur d'Alene Lake, Idaho

A reconnaissance study of Coeur d'Alene Lake, Idaho done from May through November 1987 assessed water quality throughout the lake. Particular emphasis was on hypolimnetic concentrations of dissolved oxygen, nutrients, and trace elements. Study results enabled refinement of the sampling protocol in a U.S. Geological Survey research proposal for a large-scale investigation of nutrient enrichment and trace element contamination problems affecting the 129.5 sq kilometer lake in northern Idaho. Hypolimnetic dissolved-oxygen concentrations as low as 4.1 mg/L in November and the frequent occurrence of supersaturated dissolved-oxygen concentrations during June through August indicated nutrient enrichment. Secchi-disc depths in the lake 's central and southern areas were typical of mesotrophic conditions, whereas oligotrophic conditions prevailed in the northern area. Throughout the study, hypolimnetic concentrations of total recoverable zinc exceeded chronic and acute toxicity criteria for freshwater aquatic life. (USGS)

Water-Resources Investigations Report

Streamflow, dissolved solids, suspended sediment, and trace elements, San Joaquin River, California, June 1985-September 1988

The 1985-88 study period included hydrologic extremes throughout most of central California. Except for an 11-month period during and after the 1986 flood, San Joaquin River streamflows during 1985-88 were generally less than median for 1975-88. The Merced Tuolumne, and Stanislaus Rivers together comprised 56 to 69 percent of the annual San Joaquin River flow, Salt and Mud Sloughs together comprised 6 to 19 percent, the upper San Joaquin River comprised 2 to 25 percent, and unmeasured sources from agricultural discharges and ground water accounted for 13 to 20 percent. Salt and Mud Sloughs and the unmeasured sources contribute most of the dissolved-solids load. The Merced, Tuolumne, and Stanislaus Rivers greatly dilute dissolved-solids concentrations. Suspended-sediment concentration peaked sharply at more than 600 milligrams per liter during the flood of February 1986. Concentrations and loads varied seasonally during low-flow conditions, with concentrations highest during the early summer irrigation season. Trace elements present primarily in dissolved phases are arsenic, boron, lithium, molybdenum, and selenium. Boron concentrations exceeded the irrigation water-quality criterion of 750 micrograms per liter more than 75 percent of the time in Salt and Mud Sloughs and more than 50 percent of the time at three sites on the San Joaquin River. Selenium concentrations exceeded the aquatic-life criterion of 5 micrograms per liter more than 75 percent of the time in Salt Slough and more than 50 percent of the time in Mud Slough and in the San Joaquin River from Salt Slough to the Merced River confluence. Concentrations of dissolved solids, boron, and selenium usually are highest during late winter to early spring, lower in early summer, higher again in mid-to-late summer, and the lowest in autumn, and generally correspond to seasonal inflows of subsurface tile-drain water to Salt and Mud Sloughs. Trace elements present primarily in particulate phases are aluminum, chromium, copper, iron, manganese, nickel, and zinc, none of which cause significant water-quality problems in the river.

California

Surface-water-quality assessment of the lower Kansas River Basin, Kansas and Nebraska: Distribution of trace-element concentrations in dissolved and suspended phases, streambed sediment, and fish samples, May 1987 through April 1990

The distribution of trace elements in dissolved and suspended phases, streambed sediment, and fish samples is described for principal streams in the lower Kansas River Basin, Kansas and Nebraska, from May 1987 through April 1990. Large median concentrations of dissolved lithium and strontium in the Kansas River were related to saline ground-water discharge, and large median concentrations of dissolved strontium in Mill Creek near Paxico, Kansas were related to Permian limestone and shale. Large concentrations of arsenic, chromium, and lead in water were identified downstream from three reservoirs, which may be attributed to resuspension of bed sediment in turbulent flow near the dams or release of water from near the bottom of the reservoirs. Trace elements in streambed sediments greater than background concentrations were identified downstream from the Aurora, Nebraska, wastewater-treatment plant, from industrial or urban areas near Kansas City, Kansas, and from the dam at Perry Lake, Kansas. Median and 90th-percentile concentrations of mercury in fish-tissue samples approximately doubled from 1979-86 to 1987-90. However, concentrations in samples collected during the latter period were less than the National Academy of Sciences and National Academy of Engineering 1972 criterion of 500 micrograms per kilogram for mercury in fish tissue.

Kansas, Nebraska

Geographical distribution and potential for adverse biological effects of selected trace elements and organic compounds in streambed sediment in the Connecticut, Housatonic, and Thames River basins, 1992-94

Streambed-sediment samples were collected in 1992-94 at selected sites in the Connecticut, Housatonic, and Thames River Basins to determine the geographical distribution of trace elements and organic compounds and their potential for adverse biological effects on aquatic organisms. Chromium, copper, lead, mercury, nickel, zinc, chlordane, DDT, PAHs, and PCBs were detected in samples from throughout the basins, but concentrations of these constituents generally were lowest in the northern forested drainage basins and highest in the southern urbanized drainage basins of Springfield, Massachusetts, and Hartford, New Haven and Bridgeport, Connecticut. Possible anthropogenic sources of these contaminants include industrial effluent; municipal wastewater; runoff from agricultural, urban and forested areas; and atmospheric deposition. Some organic compounds pose the greatest threat to biological organisms in terms of exceedances of sediment-quality guidelines; those compounds are present at sufficiently high concentrations to potentially cause severe effects at several locations in the basins. Some trace elements represent the most geographically widespread threat to living organisms. These exceed sediment-quality guidelines over a wider geographical area, although usually by lower ratios of contaminant concentration to sediment-quality guideline than the organic compounds.

Connecticut, Massachusetts, New Hampshire, New Yor

Assimilation and retention of selenium and other trace elements from crustacean food by juvenile striped bass (Morone saxatilis)

Estimates of the assimilation and retention of trace elements from food by fish are useful for linking toxicity with the biogeochemical cycling of these elements through aquatic food webs. Here we use pulse-chase radiotracer techniques to estimate the assimilation and retention of Se and four trace metals, Ag, Am, Zn, and Cd, by 43- and 88-d-old juvenile striped bass, Morone saxatilis, from crustacean food. Brine shrimp nauplii, Artemia franciscana , or adult copepods, Acartia tonsa , were fed radiolabeled diatoms and then fed to juvenile striped bass. Assimilation efficiencies (AEs ± SD) for 43-d-old fish were 18 ± 2%, 6 ± 1%, 23 ± 4%, 33 ± 3%, and 23 ± 2% for Ag, Am, Cd, Se, and Zn, respectively. For 88-d-old fish, the AEs were 28 ± 1%, 42 ± 5%, and 40 ± 5% for Cd, Se, and Zn, respectively. The higher AEs in the older fish may result from longer gut passage times for larger fish. The 44-d-old fish excreted 5 ± 0.8%, 4 ± 2.0%, 7 ± 0.3%, 9 ± 0.4%, and 1.3 ± 0.9% of the Ag, Am, Cd, Se, and Zn, respectively, they ingested from food per day, whereas the 88-d-old fish excreted 3 ± 1.0%, 8 ± 0.5%, and 3 ± 0.5% of the assimilated Cd, Se, and Zn per day, respectively. Predictions of steady state Se concentrations in juvenile striped bass tissues made using a biokinetic model and the measured AE and efflux rates ranged from 1.8 to 3.0 mg Se g -1 dry wt for muscle tissue and 6.8 to 11.6 mg Se g -1 dry wt for gut tissue. These predictions agreed well with average values of 2.1 and 13 mg Se g -1 dry wt measured independently in North San Francisco Bay, where elevated Se concentrations are of concern. The model results imply that the planktonic food web, including juvenile striped bass, does not transfer Se as efficiently to top consumers as does the benthic food web.

Limnology and Oceanography

Accumulation of trace elements and organochlorines by surf scoters wintering in the Pacific northwest

Selenium, cadmium, mercury, copper, manganese, zinc, aluminum, lead, PCBs and DDE were accumulated by segments of the surf scoter (Melanitta perspicillata) population that winters in the Pacific Northwest, but whether the uptake occurred on breeding and/or wintering grounds was uncertain for some contaminants. Surf scoters collected in Puget Sound and San Francisco Bay (in another study) during the same period (January 1985) contained similar concentrations of cadmium, but Alsea Bay scoters contained more. Cadmium was inversely related to both liver and body weights of Northwest scoters in January; similar weight losses were reported in experimental laboratory studies. Northwest and north San Francisco Bay scoters contained similar mercury concentrations, but those in south San Francisco Bay contained higher concentrations. San Francisco Bay scoters contained higher arsenic and selenium concentrations than those in the Northwest; however, the 43.4 ppm (geometric mean, dry wt) selenium in livers at Commencement Bay in January was above levels associated with the reproductive problems in aquatic birds at Kesterson National Wildlife Refuge. Even higher concentrations of some elements may be found in surf scoters in March, because a later collection (March) at San Francisco Bay yielded higher concentrations than found there in January. Trace element concentrations in birds at a given wintering location are variable among species and may be influenced by diet, breeding grounds, and physiology (e.g., at Commencement Bay surf scoters with a sediment-associated diet contained 50X more cadmium in their kidneys than did fish-eating western grebes [Aechmophorus occidentalis]). The numerous wildlife species that live on estuaries require further attention.

Northwestern Naturalist

Sampling and major element chemistry of the recent (A.D. 1631-1944) Vesuvius activity

Detailed sampling of the Vesuvius lavas erupted in the period A.D. 1631-1944 provides a suite of samples for comprehensive chemical analyses and related studies. Major elements (Si, Ti, Al, Fetotal, Mn, Mg, Ca, Na, K and P), volatile species (Cl, F, S, H2O+, H2O- and CO2), and ferrous iron (Fe2+) were determined for one hundred and forty-nine lavas and five tephra from the A.D. 1631-1944 Vesuvius activity. The lavas represent a relatively homogeneous suite with respect to SiO2, TiO2, FeOtotal, MnO and P2O5, but show systematic variations among MgO, K2O, Na2O, Al2O3 and CaO. The average SiO2 content is 48.0 wt.% and the rocks are classified as tephriphonolites according to their content of alkalis. All of the lavas are silica-undersaturated and are nepheline, leucite, and olivine normative. There is no systematic variation in major-element composition with time, over the period A.D. 1631-1944. The inter-eruption and intra-eruption compositional differences are the same magnitude. The lavas are highly porphyritic with clinopyroxene and leucite as the major phases. Fractionation effects are not reflected in the silica content of the lavas. The variability of MgO, K2O, Na2O, and CaO can be modelled as a relative depletion or accumulation of clinopyroxene. ?? 1993.

Journal of Volcanology and Geothermal Research

NASQAN: The design and implementation of a large-river suspended sediment and trace element flux programme

In 1996 the US Geological Survey (USGS) began a national flux-based water quality monitoring programme in the Mississippi, Columbia, Colorado, and Rio Grande basins. Suspended sediment flux estimates for periods greater than a year are generally accurate within ??15%. Discharge and suspended sediment concentrations varied much more than chemical levels. Most trace element concentrations are not elevated except Zn and Hg in the Ohio River, and Ag, Cu, Pb, Zn, Cd, Cr, Co, Ba, Mo, Sb, Hg, and Fe in the upper Columbia River, which is impacted by mining waste. The majority (???70%) of Cu, Zn, Cr, Ni, Ba, P, As, Fe, Mn, and Al are transported by suspended sediment; Sr transported seems dominated by the dissolved phase, whereas the transport of Li and TOC seem to be divided equally between both phases.In 1996 the US Geological Survey (USGS) began a national flux-based water quality monitoring programme in the Mississippi, Columbia, Colorado, and Rio Grande basins. Suspended sediment flux estimates for periods greater than a year are generally accurate within ??15%. Discharge and suspended sediment concentrations varied much more than chemical levels. Most trace element concentrations are not elevated except Zn and Hg in the Ohio River, and Ag, Cu, Pb, Zn, Cd, Cr, Co, Ba, Mo, Sb, Hg, and Fe in the upper Columbia River, which is impacted by mining waste. The majority (???70%) of Cu, Zn, Cr, Ni, Ba, P, As, Fe, Mn, and Al are transported by suspended sediment; Sr transported seems dominated by the dissolved phase, whereas the transport of Li and TOC seem to be divided equally between both phases.

Conference Paper

Changes in sediment-associated trace element concentrations in the Seine river basin (1994-2001)

In the 1980's, based on the concentrations of particulate-associated Hg, Cd, Pb, Cu and Zn relative to very low natural background levels, the Seine River Basin was one of the most impacted in the world. Over the past 20 years, there has been a general decline in these elevated concentrations that parallels declines in Paris sewage sludge trace element levels. Within the basin, marked differences in spatial and temporal geochemical patterns have been observed: (1) between major tributaries, (2) between trace elements, and (3) with stream order and population density, all of which illustrate the complexity of the geochemical processes ongoing in the basin.

Conference Paper

Defining fish nursery habitats: An application of otolith elemental fingerprinting in Tampa Bay, Florida

Fishing in Tampa Bay enhances the quality of life of the area's residents and visitors. However, people's desire to settle along the Bay's shorelines and tributaries has been detrimental to the very habitat believed to be crucial to prime target fishery species. Common snook (Centropomus undecimalis) and red drum (Sciaenops ocellatus) are part of the suite of estuarine fishes that 1) are economically or ecologically prominent, and 2) have complex life cycles involving movement between open coastal waters and estuarine nursery habitats, including nursery habitats that are located within upstream, low-salinity portions of the Bay?s tidal tributaries. We are using an emerging microchemical technique -- elemental fingerprinting of fish otoliths -- to determine the degree to which specific estuarine locations contribute to adult fished populations in Tampa Bay. In ongoing monitoring surveys, over 1,000 young-of-the-year common snook and red drum have already been collected from selected Tampa Bay tributaries. Using laser ablation-inductively coupled plasma - mass spectrometry (LA-ICP-MS), we are currently processing a subsample of these archived otoliths to identify location-specific fingerprints based on elemental microchemistry. We will then analyze older fish from the local fishery in order to match them to their probable nursery areas, as defined by young-of-the-year otoliths. We expect to find that some particularly favorable nursery locations contribute disproportionately to the fished population. In contrast, other nursery areas may be degraded, or act as 'sinks', thereby decreasing their contribution to the fish population. Habitat managers can direct strategic efforts to protect any nursery locations that are found to be of prime importance in contributing to adult stocks.

Florida

Spectrochemical determination of trace elements in galena

A semiquantitative spectrochemical method is described by means of which 10-mg samples of galena can be analyzed for their trace element content. Results on 40 elements are reported as six logarithmically spaced intervals per order of magnitude and obtained by visual comparison with standards prepared in spectrographically pure lead sulfide. Detection limits are generally between 1 and 20 ppm (except for Ce, Na, Sr, Ta, and Zn, which are 50 to 100 ppm). Replicate analyses of galena samples indicate a precision comparable to other semiquantitative spectrochemical methods used for the analysis of geochemical samples. Results obtained from the analysis of 129 galena samples are summarized.

Journal of Research of the U.S. Geological Survey

Chemical weathering of the Panola Granite: Solute and regolith elemental fluxes and the weathering rate of biotite

Present-day elemental and mineral weathering rates based on solute fluxes are compared quantitatively to past long-term rates determined from solid-state elemental fractionation in a saprolitic granite regolith at Panola, Georgia, USA. Saturated fluid flow across a low-permeability kaolin duripan controls the rate of steady-state unsaturated flow in the underlying saprolite. Water and Cl mass balances and experimental conductivities produce a minimum fluid flux density of 8x10 -2 m yr -1 and a fluid residence time of 12 years. Solute Si flux, based on pore water concentrations and infiltration rates, is 27 mmoles yr -1 , compared to a long-term flux rate of 17 mmoles yr -1 , based on regolith Si loss and reported 36 Cl dating of the regolith surface. Similarities in short- and long-term fluxes imply that parameters influencing silicate weathering, including precipitation, temperature, and vegetative cover, while not necessarily constant, have not significantly impacted Si leaching rates during the last several hundred thousand years. Linear decreases in solid-state Mg with decreasing regolith depth permit the calculation of the long-term biotite weathering rate under isovolumetric steady-state weathering conditions. A rate constant of 3x10 -17 moles m -2 s -1 is up to 5 orders of magnitude slower than that reported for experimental dissolution of biotite, implying very different reaction kinetics during natural weathering. Short-term biotite weathering fails to produce expected increases in solute Mg and K concentrations with increasing depth and fluid residence times in the regolith. This discrepancy indicates that ion exchange disequilibrium and open-system biologic uptake in an aggrading forest ecosystem are of sufficient magnitudes to overwhelm solute fluxes resulting from biotite weathering.

Georgia

187Os/188Os And Highly Siderophile Element Systematics Of Apollo 17 Aphanitic Melt Rocks

Generally chondritic relative abundances and high absolute abundances of the highly siderophile elements (HSE: Ru, Rh, Pd, Re, Os, Ir, Pt, Au) in Earth's upper mantle provide strong evidence that these elements were added to the Earth following the last major interaction between its metallic core and silicate fraction. So called "late accretion" may have added materials comprising as much as 0.8% of the total mass of the Earth and possibly a similar proportion of mass to the Moon. We have begun to study the chemical nature of late accreted materials to the Earth-Moon system by examining the HSE contained in lunar impact-melt rocks. The HSE contained in melt rocks were largely added to the Moon during the period of time from the origin of the lunar highlands crust (4.4-4.5 Ga) to the end of the late bombardment period (ca. 3.9 Ga). These materials provide the only direct chemical link to the late accretionary period. The chemical fingerprints of the HSE in late accreted materials may enable us to ascertain under what conditions and where in the solar system the late accreted materials formed. The 1870s/1880s ratios (reflecting long-term Re/Os), coupled with ratios of other HSE, can be diagnostic for identifying the nature of the impactor. A critical issue, however, will be deconvolving the exogenous from indigenous components. Herein we examine the Os isotopic and HSE systematics of Apollo 17 aphanitic melt rocks 73215 and 73255. The HSE in these rocks were likely added at ~3.9 Ga from the impactor that formed the Serenitatis basin.

Conference Paper

Interagency Ecological Program long-term monitoring element review: Pilot approach and methods development (2020)

This report describes the first-year, pilot-phase of what is intended to be a larger, multiple-year review of all IEP core long-term monitoring elements (LTMEs). Here we hope to provide evidence that the review team arrangement and communication schedule was effective at developing a framework to objectively evaluate a suite of LTMEs. We focused on developing methods for an effective review, documenting the process of methods development, and compiling recommendations for applications of these methods to future reviews. We also gathered recommendations to improve data collection, catchability-adjustment, and record keeping processes which will be useful for all LTMEs regardless of when they are to be reviewed. Although we did not complete a comprehensive review of the long-term monitoring elements due to our short timeline, we believe this report represents a substantial effort towards that review and will serve as an invaluable guide for subsequent IEP LTME reviews.

Report