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Vincent Ellis McKelvey

Publications and source records attributed to Vincent Ellis McKelvey.

15 recordsLinked to original sources
USGS1983

Analysis of the world distribution of metal-rich subsea manganese nodules

Publicly available data on the composition of subsea manganese nodules extend previous reports of differences in average metal contents from ocean to ocean and of variations related to latitude and depth. Pacific Ocean nodules have the highest average manganese, nickel, and copper contents, and Atlantic Ocean nodules have the highest average iron content. The average manganese, nickel, and copper contents generally increase toward the equator in both hemispheres, and iron content generally decreases. The variation of metal content with water depth is not linear; instead, there appears to be a threshold depth of about 2,900 to 3,000 m, above which combined nickel and copper contents are generally less than 1 percent and below which cobalt content is generally less than about 0.6 percent. The composition of the nodules varies widely, but three rarely overlapping types that are of possible economic interest can be recognized. (1) Nodules containing more than about 1 percent combined nickel and copper only exceptionally contain more than 0.5 percent cobalt and 35 percent manganese. (2) Nodules containing more than 0.5 percent cobalt rarely contain more than 1 percent combined nickel and copper and 35 percent manganese. (3) Nodules containing more than 35 percent manganese only exceptionally contain more than 0.5 percent cobalt, although they average nearly 1.1 percent combined nickel and copper. Current economic interest in nodule mining is focused on the Clarion-Clipperton zone in the northeastern equatorial Pacific Ocean, the largest known area in which nodules average 1.8 percent or more combined nickel and copper. Several other areas in which nodules are rich in these metals are found in the Pacific and Indian Oceans and may be viewed as targets for exploration. Nearly 60 chemical elements have been found in manganese nodules, many in concentrations far exceeding their crustal abundances. The amounts in which many minor elements are present vary with the amounts of principal metals present, but the three metal types described above do not include the maximum reported values for several other elements, such as titanium (8.9 percent), vanadium (0.5), zinc (9.0), and lead (0.75). It seems possible, therefore, that there may be other kinds of metal-rich types, some of which may have p6tential economic value. Many of the variations in nodule composition are in large part a function of variations in mineral composition, to which many factors contribute. Some of the regional variations can be broadly related to oceanic circulation, basin morphology, and depth, but a better understanding of ocean processes and regional oceanography and geology is needed to explain all the variations observed in the composition of manganese nodules.

Circular↗
USGS1955

Uranium in the Upper Cambrian black shale of Sweden

The Peltura zone of the Upper Cambrian black shales of Sweden contains about 0.02 percent uranium. Maximum amounts are present in rocks deposited in an embayment in the sea and in rocks in or closely adjacent to that part of the vertical sequence that contains maximum amounts of distillable oil, total organic matter, pyrite, and a black highly uraniferous kerogen called "kolm". Available data suggest that the precipitation of uranium is favored by a low redox potential and that the uranium in the shale matrix may be in fine-grained kolm.

Trace Elements Investigations↗
USGS1953

Search for uranium in western United States

The search for uranium in the United States is one of the most intensive ever made for any metal during our history. The number of prospectors and miners involved is difficult to estimate but some measure of the size of the effort is indicated by the fact that about 500 geologists are employed by government and industry in the work--more than the total number of geologists engaged in the study of all other minerals together except oil. The largest part of the effort has been concentrated in the western states. No single deposit of major importance by world standards has been discovered but the search has led to the discovery of important minable deposits of carnotite and related minerals on the Colorado Plateau; of large, low grade deposits of uranium in phosphates in the northwestern states and in lignites in the Dakotas, Wyoming, Idaho and New Mexico; and of many new and some promising occurrences of uranium in carnotite-like deposits and in vein deposits. Despite the fact that a large number of the districts considered favorable for the occurrence of uranium have already been examined, the outlook for future discoveries is bright, particularly for uranium in vein and in carnotite-like deposits in the Rocky Mountain States.

Trace Elements Investigations↗
USGS1952

Stratigraphic sections of the Phosphoria formation in Idaho, 1947-48, Part I

The Permian Phosphoria formation of the western states contains one of the world's largest reserves of phosphate. Although previous investigations (see especially Mansfield, 1927), including reconnaissance geologic mapping and sampling, established the location of most of the important deposits and their quality of scattered localities, they were not sufficiently detailed to permit a comparison of the merits of individual deposits or an appraisal of the reserves of phosphate rock that might be available under present economic conditions. Because the growing importance of the western phosphate deposits requires a better, more detailed understanding of their distribution and quality, the Geological Survey began in 1947 a comprehensive investigation, including (1) reconnaissance geologic mapping, mostly in Montana, of areas in which the Phosphoria formation could occur but where it had not previously been looked for or found; (2) geologic mapping, mostly in Montana, at a scale no smaller than 1:62,500, of several areas known to contain the Phosphoria formation but not previously mapped except in reconnaissance fashion; (3) geologic and topographic mapping, at a scale of 1:12,000, of some of the richest, thickest, and most accessible deposits; (4) measuring, describing, and sampling all beds of the phosphatic and shaly parts, and in some places the full thickness, of the Phosphoria formation and its stratigraphic equivalents at one or two localities per township over the entire field; (5) chemical and spectrographic analysis of the samples for phosphate, fluorine, minor metals, oil, and rock-forming constituents; and (6) petrologic and geochemical studies of the rocks and minerals of the formation. These studies are designed to define the regional and local geologic structures in which the phosphate bed lie, to provide a basis for the estimation of reserves of the inferred class over the entire region, and to determine the origin of the rocks and the elements contained in them. The data collected are not of the detail required to plan actual mining operations, but it is hoped they will guide industry in the selection of individual deposits worthy of further exploration. Most of the field work contemplated as a part of this investigation is now completed. Although the data will not be compiled or published in final form for some years to come, segments of the data, accompanied by little or no interpretation, will be published as preliminary maps or reports as they are assembled. The present report is the first of a series presenting in abbreviated form the description and analyses of the beds measured and sampled at various localities in southeastern Idaho (pl. 1). Companion reports presenting segments of the data from Montana, Wyoming, and Utah (Swanson and others, 1952, and McKelvey and others, 1952a and 1952b) are being released at the same time as this report, and others are in preparation.

Idaho↗
USGS1952

Stratigraphic sections of the Phosphoria formation in Wyoming, 1947-48

As part of a comprehensive investigation of the phosphate deposits of the western field begun in 1947, the U. S. Geological Survey has measured and sampled the Permian Phosphoria formation at many localities in Wyoming and adjacent states. Because these data will not be fully synthesized for many years, segments of the data, accompanied by little or no interpretation, will be published as preliminary reports as they are assembled. This report, which contains abstracts of some of the sections measured in western Wyoming (pl. 1), is one of this series. The field and laboratory procedures adopted in these investigations are described rather fully in a companion report (McKelvey and others, 1952a). Many people have taken part in this investigation. R. M. Campbell, R. A. Gulbrandsen, R. A. Harris, D. M. Larrabee, F. W. O'Malley, O. A. Payne, R. S. Sears, R. P. Sheldon, and R. A. Smart participated in the description of the strata and the collection of the samples referred to in this report. D. B. Dimick, H. A. Larsen, and T. K. Rigby assisted in the preparation of exposures and the crushing and splitting of samples in the field. The laboratory preparation of samples for chemical analysis was done in Denver, Colo., under the direction of W. P. Huleatt. Most of the P 2 O 5 and acid-insoluble analyses were made for the Survey by the U. S. Bureau of Mines at the Northwest Electrodevelopment Laboratory, Albany, Oreg., under the direction of S. M. Shelton and M. L. Wright. Most of the Al 2 O 3 , Fe 2 O 3 , and loss-on-ignition analyses were made by the Trace Elements Section laboratory of the Survey in Washington, D. C., under the direction of J. C. Rabbitt by chemists I. Barlow, A. Caemmerer, J. Greene, F. S. Grimadli, N. Guttag, H. Levine, H. Mela, Jr., and R. G. Milkey, and most of the spectrographic reports were prepared in this laboratory by C. L. Waring. The samples from one locality (Coal Canyon) were analyzed for P 2 O 5 , Al 2 O 3 , Fe 2 O 3 , V 2 O 5 , F, loss on ignition, and acid insoluble in the Chemical Laboratory of the Tennessee Valley Authority at Wilson Dam, Alabama, and spectrographically by D. M. Mortimer, of the Bureau of Mines at Albany. Compilation of the data has been largely by R. P. Sheldon and F. D. Frieske under the supervision of R. W. Swanson. Organization of the tabular data has been largely by Anita Cozzetto.

Wyoming↗
USGS1952

Stratigraphic sections of the Phosphoria formation in Utah, 1947-48

As part of a comprehensive investigation of the phosphate deposits of the western field begun in 1947, the U. S. Geological survey has measured an sampled the full thickness of the Permian Phosphoria formation and its partial correlative, the Park City formation, at many localities in Utah and other western states. Although these data will not be fully analyzed for several years, segments of the data, accompanied by little or no interpretation, will be published as preliminary reports. This report, which contains abstracts of many of the sections measured in northeastern Utah (pl. 1), is one of this series. The field and laboratory procedures adopted in these investigations are described rather fully in a companion report (McKelvey and others, 1952). A large number of people have taken part in this investigation. J. B. Collins, R. A. Gulbrandsen, R. A. Hoppin, J. A. Noel, F. W. O'Malley, O. A. Payne, J. F. Rominger, R. P. Sheldon, J. E. Smedley, and R. G. Waring participated in the description of strata and collection of samples referred to in this report. D. B. Dimick, H. A. Larsen, and T. K. Rigby assisted in the preparation of trenches and the crushing and splitting of samples in the field. The laboratory preparation of samples for chemical analysis was done in Denver, Colo., under the direction of W. P. Huleatt. Most of the chemical analyses reported herein were made for the Survey by the U. S. Bureau of Mines at the Northwest Electrodevelopment Laboratory, Albany, Oreg., under the direction of S. M. Shelton and M. L. Wright. All the samples from one locality (Brazer Canyon) were analyzed in the Chemical Laboratory of the Tennessee Valley Authority at Wilson Dam, Ala. Some of the Al 2 O 3 , Fe 2 O 3 , and loss-on-ignition analyses were made in the Trace Elements Section laboratory of the Survey in Washington, D. C., under the direction of J. C. Rabbitt by chemists I. Barlow, A Caemmerer, J. Greene, N. Guttag, and E. H. Humphrey. The spectrographic analyses were made by D. M. Mortimer, of the Bureau of Mines in Albany. Compilation of the data has been largely by R. P. Sheldon and F. D. Frieske under the supervision of R. W. Swanson. Organization of the tabular data has been largely by Anita Cozzetto.

Utah↗