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L. G. Woodruff

Publications and source records attributed to L. G. Woodruff.

15 recordsLinked to original sources
USGS2010

Multivariate analysis of the geochemistry and mineralogy of soils along two continental-scale transects in North America

Soils collected in 2004 along two North American continental-scale transects were subjected to geochemical and mineralogical analyses. In previous interpretations of these analyses, data were expressed in weight percent and parts per million, and thus were subject to the effect of the constant-sum phenomenon. In a new approach to the data, this effect was removed by using centered log-ratio transformations to 'open' the mineralogical and geochemical arrays. Multivariate analyses, including principal component and linear discriminant analyses, of the centered log-ratio data reveal the effects of soil-forming processes, including soil parent material, weathering, and soil age, at the continental-scale of the data arrays that were not readily apparent in the more conventionally presented data. Linear discriminant analysis of the data arrays indicates that the majority of the soil samples collected along the transects can be more successfully classified with Level 1 ecological regional-scale classification by the soil geochemistry than soil mineralogy. A primary objective of this study is to discover and describe, in a parsimonious way, geochemical processes that are both independent and inter-dependent and manifested through compositional data including estimates of the elements and corresponding mineralogy. ?? 2010.

Science of the Total Environment↗
USGS2009

Pilot studies for the North American Soil Geochemical Landscapes Project - Site selection, sampling protocols, analytical methods, and quality control protocols

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada sampled and chemically analyzed soils along two transects across Canada and the USA in preparation for a planned soil geochemical survey of North America. This effort was a pilot study to test and refine sampling protocols, analytical methods, quality control protocols, and field logistics for the continental survey. A total of 220 sample sites were selected at approximately 40-km intervals along the two transects. The ideal sampling protocol at each site called for a sample from a depth of 0-5 cm and a composite of each of the O, A, and C horizons. The <2-mm fraction of each sample was analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y, and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO 3 , HClO 4 , and HF. Separate methods were used for Hg, Se, total C, and carbonate-C on this same size fraction. Only Ag, In, and Te had a large percentage of concentrations below the detection limit. Quality control (QC) of the analyses was monitored at three levels: the laboratory performing the analysis, the USGS QC officer, and the principal investigator for the study. This level of review resulted in an average of one QC sample for every 20 field samples, which proved to be minimally adequate for such a large-scale survey. Additional QC samples should be added to monitor within-batch quality to the extent that no more than 10 samples are analyzed between a QC sample. Only Cr (77%), Y (82%), and Sb (80%) fell outside the acceptable limits of accuracy (% recovery between 85 and 115%) because of likely residence in mineral phases resistant to the acid digestion. A separate sample of 0-5-cm material was collected at each site for determination of organic compounds. A subset of 73 of these samples was analyzed for a suite of 19 organochlorine pesticides by gas chromatography. Only three of these samples had detectable pesticide concentrations. A separate sample of A-horizon soil was collected for microbial characterization by phospholipid fatty acid analysis (PLFA), soil enzyme assays, and determination of selected human and agricultural pathogens. Collection, preservation and analysis of samples for both organic compounds and microbial characterization add a great degree of complication to the sampling and preservation protocols and a significant increase to the cost for a continental-scale survey. Both these issues must be considered carefully prior to adopting these parameters as part of the soil geochemical survey of North America.

Applied Geochemistry↗
USGS2009

Continental-scale patterns in soil geochemistry and mineralogy: results from two transects across the United States and Canada

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada (GSC) initiated a pilot study that involved collection of more than 1500 soil samples from 221 sites along two continental transects across Canada and the United States. The pilot study was designed to test and refine protocols for a soil geochemical survey of North America. The two transects crossed a wide array of soil parent materials, soil ages, climatic conditions, landforms, land covers and land uses. Sample sites were selected randomly at approximately 40-km intervals from a population defined as all soils of the continent. At each site, soils representing 0 to 5 cm depth, and the O, A, and C horizons, if present, were collected and analyzed for their near-total content of over 40 major and trace elements. Soils from 0–5 cm depth were also collected for analysis of organic compounds. Results from the transects confirm that soil samples collected at a 40-km spacing reveal coherent, continental- to subcontinental-scale geochemical and mineralogical patterns that can be correlated to aspects of underlying soil parent material, soil age and climate influence. The geochemical data also demonstrate that at the continental-scale the dominance of any of these major factors that control soil geochemistry can change across the landscape. Along both transects, soil mineralogy and geochemistry change abruptly with changes in soil parent materials. However, the chemical influence of a soil’s parent material can be obscured by changing climatic conditions. For the transects, increasing precipitation from west to east and increasing temperature from north to south affect both soil mineralogy and geochemistry because of climate effects on soil weathering and leaching, and plant productivity. Regional anomalous metal concentrations can be linked to natural variations in soil parent materials, such as high Ni and Cr in soils developed on ultramafic rocks in California or high P in soils formed on weathered Ordovician limestones in central Kentucky. On local scales, anomalous metal concentrations recognized in soil profiles, such as high P in soils from animal confinement sites, are consistent with local anthropogenic disturbances. At a larger scale, the distribution of Hg across the west to east transect demonstrates that it can be difficult to distinguish between natural or anthropogenic contributions and that many factors can contribute to an element’s spatial distribution. Only three samples in a subset of seventy-three 0–5 cm depth soil samples from the north to south transect had organochlorine pesticides values above the method detection limit, apparently related to historic usage of the pesticides DDT and dieldrin.

Applied Geochemistry↗
USGS2006

Mercury in soils, lakes, and fish in Voyageurs National Park (Minnesota): Importance of atmospheric deposition and ecosystem factors

Concentrations of methylmercury in game fish from many interior lakes in Voyageurs National Park (MN, U.S.A.) substantially exceed criteria for the protection of human health. We assessed the importance of atmospheric and geologic sources of mercury to interior lakes and watersheds within the Park and identified ecosystem factors associated with variation in methylmercury contamination of lacustrine food webs. Geologic sources of mercury were small, based on analyses of underlying bedrock and C-horizon soils, and nearly all mercury in the O- and A-horizon soils was derived from atmospheric deposition. Analyses of dated sediment cores from five lakes showed that most (63% ?? 13%) of the mercury accumulated in lake sediments during the 1900s was from anthropogenic sources. Contamination of food webs was assessed by analysis of whole, 1-year-old yellow perch (Perca flavescens), a regionally important prey fish. The concentrations of total mercury in yellow perch and of methylmercury in lake water varied substantially among lakes, reflecting the influence of ecosystem processes and variables that affect the microbial production and abundance of methylmercury. Models developed with the information-theoretic approach (Akaike Information Criteria) identified lake water pH, dissolved sulfate, and total organic carbon (an indicator of wetland influence) as factors influencing methylmercury concentrations in lake water and fish. We conclude that nearly all of the mercury in fish in this seemingly pristine landscape was derived from atmospheric deposition, that most of this bioaccumulated mercury was from anthropogenic sources, and that both watershed and lacustrine factors exert important controls on the bioaccumulation of methylmercury. ?? 2006 American Chemical Society.

Environmental Science & Technology↗
USGS2004

A hydrogeologic model of stratiform copper mineralization in the Midcontinent Rift System, Northern Michigan, USA

This paper presents a suite of two-dimensional mathematical models of basin-scale groundwater flow and heat transfer for the middle Proterozoic Midcontinent Rift System. The models were used to assess the hydrodynamic driving mechanisms responsible for main-stage stratiform copper mineralization of the basal Nonesuch Formation during the post-volcanic/pre-compressional phase of basin evolution. Results suggest that compaction of the basal aquifer (Copper Harbor Formation), in response to mechanical loading during deposition of the overlying Freda Sandstone, generated a pulse of marginward-directed, compaction-driven discharge of cupriferous brines from within the basal aquifer. The timing of this pulse is consistent with the radiometric dates for the timing of mineralization. Thinning of the basal aquifer near White Pine, Michigan, enhanced stratiform copper mineralization. Focused upward leakage of copper-laden brines into the lowermost facies of the pyrite-rich Nonesuch Formation resulted in copper sulfide mineralization in response to a change in oxidation state. Economic-grade mineralization within the White Pine ore district is a consequence of intense focusing of compaction-driven discharge, and corresponding amplification of leakage into the basal Nonesuch Formation, where the basal aquifer thins dramatically atop the Porcupine Mountains volcanic structure. Equilibrium geochemical modeling and mass-balance calculations support this conclusion. We also assessed whether topography and density-driven flow systems could have caused ore genesis at White Pine. Topography-driven flow associated with the Ottawan orogeny was discounted because it post-dates main-stage ore genesis and because recent seismic interpretations of basin inversion indicates that basin geometry would not be conductive to ore genesis. Density-driven flow systems did not produce focused discharge in the vicinity of the White Pine ore district.

Michigan↗
USGS2004

Geochemistry of glacial sediments in the area of the Bend massive sulfide deposit, north-central Wisconsin

Geochemical exploration in northern Wisconsin has been problematic because of thick glacial overburden and complex stratigraphic record of glacial history. To assess till geochemical exploration in an area of thick glacial cover and complex stratigraphy samples of glacial materials were collected from cores from five rotasonic boreholes near a known massive sulfide deposit, the Bend deposit in north-central Wisconsin. Diamond drilling in the Bend area has defined a long, thin zone of mineralization at least partly intersected at the bedrock surface beneath 30-40 m of unconsolidated glacial sediments. The bedrock surface has remnant regolith and saprolite resulting from pre-Pleistocene weathering. Massive sulfide and mineralized rock collected from diamond drill core from the deposit contain high (10s to 10,000s ppm) concentrations of Ag, As, Au, Bi, Cu, Hg, Se, Te, and Tl. Geochemical properties of the glacial stratigraphic units helped clarify the sequence and source areas of several glacial ice advances preserved in the section. At least two till sheets are recognized. Over the zone of mineralization, saprolite and preglacial alluvial and lacustrine samples are preserved on the bedrock surface in a paleoriver valley. The overlying till sheet is a gray, silty carbonate till with a source hundreds of kilometers to the northwest of the study area. This gray till is overlain by red, sandy till with a source to the north in Proterozoic rocks of the Lake Superior area. The complex glacial stratigraphy confounds down-ice geochemical till exploration. The presence of remnant saprolite, preglacial sediment, and far-traveled carbonate till minimized glacial erosion of mineralized material. As a result, little evidence of down-ice glacial dispersion of lithologic or mineralogic indicators of Bend massive sulfide mineralization was found in the samples from the rotasonic cores. This study points out the importance of determining glacial stratigraphy and history, and identifying favorable lithologies required for geochemical exploration. Drift prospecting in Wisconsin and other areas near the outer limits of the Pleistocene ice sheets may not be unsuccessful, in part, because of complex stratigraphic sequences of multiple glaciations where deposition dominates over erosion. ?? 2004 Elsevier B.V. All rights reserved.

Journal of Geochemical Exploration↗
USGS2004

Some statistical relationships between stream sediment and soil geochemistry in northwestern Wisconsin - can stream sediment compositions be used to predict compositions of soils in glaciated terranes?

Mean stream sediment chemical compositions from northwestern Wisconsin in the north central United States, based on more than 800 samples, differ significantly from mean A-horizon and C-horizon soil compositions, based on about 380 samples of each horizon. Differences by a factor greater than 1.5 exist for some elements (Ca, Mn, Mg, P, Ti, Ni, Pb, Se, Zn). A very large database of stream sediment geochemistry exists for the region (more than 2200 samples) and for the U.S. (roughly 400,000 samples), whereas data on the chemistry of soils is much sparser both regionally and nationally. Therefore, we have attempted to quantify trends in compositional differences between stream sediments and nearby soils to test whether the abundant stream sediment data can be used to predict soil compositions. A simple computational technique of adjusting the stream sediment compositions according to the ratio of means of soils and stream sediments was conducted. A variety of techniques of correction and interpolation of data were tested and indicate that repetitive testing of results allows an optimum correction to be achieved. Predicted soil compositions compared to analytically determined soil compositions show a range of results from relatively good correspondence for some elements to rather poor correspondence for others. In general, predictions are best at midranges of compositions. The technique does not predict well more extreme or anomalous values. Thus, this technique appears to be useful for estimating background soil compositions and delineating regional compositional trends in soils in situations where large amounts of stream sediment analyses and smaller amounts of soil analyses are available. The technique also provides probabilistic qualifications on the expected error between predicted and actual soil compositions so that individual users can judge if the technique provides data of sufficient accuracy for specific needs. ?? 2003 Elsevier B.V. All rights reserved.

Journal of Geochemical Exploration↗
USGS2004

Bedrock geologic map of the Port Wing, Solon Springs, and parts of the Duluth and Sandstone 30' X 60' quadrangles, Wisconsin

This Open-File Report provides digital data (shapefiles and .e00 files) for the bedrock geology in the Port Wing, Solon Springs, and parts of the Duluth and Sandstone quadrangles in Wisconsin. A Miscellaneous Investigations Series map (I map) is currently in review with analogous data in paper format. This map portrays the geology of part of the Midcontinent rift system (MRS) along the southern extension of the Lake Superior syncline in northern Wisconsin. The map area contains the St. Croix horst, a rift graben filled with Mesoproterozoic rocks of the Keweenawan Supergroup that was subsequently inverted. The horst exposes about 15 - 20 km of strata that record the opening of the Midcontinent rift, its subsequent transition to a thermal subsidence basin, and eventual inversion. About 3 km of underlying Mesoproterozoic strata, including the Gogebic iron range, and about 10 km of Neoarchean rocks, exposed in the southernmost part of the map area lie to the southeast of the horst. The nearly flat-lying continental red beds of the Oronto and Bayfield Groups, the youngest strata of the Keweenawan Supergroup, overlie the volcanic rocks. A wealth of geologic data exists for the area as a result of many individual studies over the last hundred years, but much has remained unpublished in theses, dissertations, and other reports of limited availability. This map has incorporated most of that data (see list of data sources) and includes results of our investigations conducted from 1992 to 2000. Our studies were designed to fill gaps in existing data and reconcile conflicting interpretations on some aspects of the geology of the region. The purpose of this map is to complete digital coverage of quadrangles with significant exposure of rocks of the Midcontinent rift in Wisconsin and Michigan at a scale of 1:100,000. Other maps in this series include the bedrock geologic maps of the Ontonagon-Wakefield, the Ashland-Ironwood, and the Keweenaw Peninsula areas (USGS Open-File Reports 01-088 , 99-546 , and 99-149 , respectively).

Open-File Report↗
USGS1994

Geochemistry and argon thermochronology of the Variscan Sila Batholith, southern Italy: source rocks and magma evolution

The Sila batholith is the largest granitic massif in the Calabria-Peloritan Arc of southern Italy, consisting of syn to post-tectonic, calc-alkaline and metaluminous tonalite to granodiorite, and post-tectonic, peraluminous and strongly peraluminous, two-mica??cordierite??Al silicate granodiorite to leucomonzogranite. Mineral 40Ar/39Ar thermochronologic analyses document Variscan emplacement and cooling of the intrusives (293-289 Ma). SiO2 content in the granitic rocks ranges from ???57 to 77 wt%; cumulate gabbro enclaves have SiO2 as low as 42%. Variations in absolute abundances and ratios involving Hf, Ta, Th, Rb, and the REE, among others, identify genetically linked groups of granitic rocks in the batholith: (1) syn-tectonic biotite??amphibole-bearing tonalites to granodiorites, (2) post-tectonic two-mica??Al-silicate-bearing granodiorites to leucomonzogranites, and (3) post-tectonic biotite??hornblende tonalites to granodiorites. Chondrite-normalized REE patterns display variable values of Ce/Yb (up to ???300) and generally small negative Eu anomalies. Degree of REE fractionation depends on whether the intrusives are syn- or post-tectonic, and on their mineralogy. High and variable values of Rb/Y (0.40-4.5), Th/Sm (0.1-3.6), Th/Ta (0-70), Ba/Nb (1-150), and Ba/Ta (???50-2100), as well as low values of Nb/U (???2-28) and La/Th (???1-10) are consistent with a predominant and heterogeneous crustal contribution to the batholith. Whole rock ??18O ranges from ???+8.2 to +11.7???; the mafic cumulate enclaves have the lowest ??18O values and the two-mica granites have the highest values. ??18O values for biotite??honblende tonalitic and granodioritic rocks (9.1 to 10.8???) overlap the values of the mafic enclaves and two-mica granodiorites and leucogranites (10.7 to 11.7???). The initial Pb isotopic range of the granitic rocks (206Pb/204Pb ???18.17-18.45, 207Pb/204Pb ???15.58-15.77, 208Pb/204Pb ???38.20-38.76) also indicates the predominance of a crustal source. Although the granitic groups cannot be uniquely distinguished on the basis of their Pb isotope compositions most of the post-tectonic tonalites to granodiorites as well as two-mica granites are somewhat less radiogenic than the syn-tetonic tonalites and granodiorites. Only a few of the mafic enclaves overlap the Pb isotope field of the granitic rocks and are consistent with a cogenetic origin. The Sila batholith was generated by mixing of material derived from at least two sources, mantle-derived and crustal, during the closing stages of plate collision and post-collision. The batholith ultimately owes its origin to the evolution of earlier, more mafic parental magmas, and to complex intractions of the fractionating mafic magmas with the crust. Hybrid rocks produced by mixing evolved primarily by crystal fractionation although a simple fractionation model cannot link all the granitic rocks, or explain the entire spectrum of compositions within each group of granites. Petrographic and geochemical features characterizing the Sila batholith have direct counterparts in all other granitic massifs in the Calabrian-Peloritan Arc. This implies that magmatic events in the Calabrian-Peloritan Arc produced a similar spectrum of granitic compositions and resulted in a distinctive type of granite magmatism consisting of coeval, mixed, strongly peraluminous and metaluminous granitic magmas. ?? 1994 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1987

Sulfur and lead isotope studies of stratiform Zn-Pb-Ag deposits, Anvil Range, Yukon: Basinal brine exhalation and anoxic bottom-water mixing (Canada)

Five stratiform Zn-Pb-Ag deposits are known in Early Cambrian metapelitic rocks along a curvilinear trend in the Anvil Range, central Yukon. The Anvil Range deposits occur along the southwestern boundary of the Selwyn basin in the stratigraphic transition zone between metapelites of the Mt. Mye unit and calcareous phyllites of the overlying Vangorda unit. The massive sulfides are associated closely with anomalously thick graphitic phyllites, apparently related to a second-order basin. A typical Anvil cycle of mineralization begins with a ribbon-banded graphitic-quartzitic-pyritic unit. This grades upward into sulfide-bearing quartzite, quartzitic massive sulfide, massive sulfide, and finally a baritic massive sulfide horizon. Sericitic alteration envelopes irregularly encompass each deposit and locally are developed best in footwall rocks. Detailed sulfur isotope studies have been carried out on the DY and Grum deposits and on one representative drill hole from the Faro deposit. The delta 34 S values of sulfide minerals generally range from 10 to 22 per mil and are similar in all three deposits. The delta 34 S values of pyrite in unmineralized samples from the district exhibit a wider range, from 6 to 34 per mil, and show distinct upward stratigraphic increase due to a stagnation cycle in the basin. The delta 34 S values of barite samples are strongly dependent on bottom-water conditions and mode of mixing during brine exhalation. They range from 22 to 26 per mil in the Faro deposit to 36 to 42 per mil in the DY deposit. These variations are due to mixing of isotopically light sulfate (18-20ppm) in Ba-bearing ore fluid and isotopically heavy residual sulfate (30-60ppm) in anoxic seawater. Thirty-eight samples of galena from the DY, Grum, Faro, SB, and Swim deposits have been analyzed for lead isotope ratios. In general, the lead isotope ratio data indicate an upper crustal lead source, with the Proterozoic Grit unit which is inferred to underlie the district being the most likely source rock. A small component of mantle leads from mafic igneous rocks or due to source rock inhomogeneity is also indicated. Graphitic host lithologies, lack of stratiform iron oxides, delta 34 S values of sedimentary pyrite, and sulfide sulfur-organic carbon variations in unmineralized cores indicate formation of the Anvil deposits in strongly reduced bottom water related to a previously unknown Early Cambrian anoxic event.

Economic Geology↗
USGS1980

Oxygen isotopic determinations of sequentially erupted plagioclases in the 1974 magma of Fuego Volcano, Guatemala

Plagioclases in the 1974 high-Al basalt from Fuego Volcano have ??O18 values of +6.0 to +8.5 per mil. Meteoric water cannot have played a significant role in Fuego's magma. Large, weakly zone clear phenocrysts had ??O18 values in the accepted mantle range, while patchyzoned and oscillatory-zoned plagioclases inferred to have formed later and shallower levels have slightly heavier oxygen isotopic ratios. ?? 1980 Intern. Association of Volcanology and Chemistry of the Earth's Interior.

Bulletin Volcanologique↗