The Vendian record of Sr and C isotopic variations in seawater: Implications for tectonics and paleoclimate

New Sr and C isotopic data, both obtained on the same samples of marine carbonates, provide a relatively detailed record of isotopic variation in seawater through the latest Proterozoic and allow, for the first time, direct correlation of these isotopic changes in the Vendian ( 540–610 Ma). The strong isotope variations determined in this study record significant environmental and tectonic changes. Together with a fairly poorly constrained Nd isotopic record, the Sr and C isotopic records can be used to constrain rates of erosion, hydrothermal alteration and organic C burial. Further, comparison of these records with those of the Cenozoic permit investigation of the general relationship between global tectonics and continental glaciation. In particular, results of this study show a very large change in the ⁸⁷Sr/⁸⁶Sr of marine carbonates from low pre-Vendian ( > 610 Ma) values ( 0.7066) to high Middle Cambrian values ( 0.7090). This change is greater in magnitude than the significant increase in seawater ⁸⁷Sr/⁸⁶Sr through the Cenozoic. Both changes are attributed to high erosion rates associated with continent-continent collisions (Pan-African and Himalayan-Tibetan). In the latest Proterozoic these high erosion rates, probably coupled with high organic productivity and anoxic bottom-water conditions, contributed to a significant increase in the burial rate of organic C. Ice ages mark both the Neoproterozoic and Cenozoic, but different stratigraphic relationships between the Sr isotopic increase and continental glaciation indicate that uplift-driven models proposed to explain Cenozoic climatic change cannot account for the latest Proterozoic ice ages.     

Sulfur dioxide and dimethyl sulfide in the central Pacific troposphere

Boundary-layer and free-troposphere measurements of sulfur dioxide, dimethyl sulfide, and carbon disulfide were made during transits of the central and southern Pacific Ocean between Hawaii and Australia. Sulfur dioxide was generally less than 100 pptv and highly variable with no correlation with respect to geographic location or altitude. Dimethyl sulfide in the boundary layer had a concentration range of <10 to 200 pptv. Highest concentrations of DMS were in the equatorial region of the southern hemisphere although the concentrations were dependent on location and meteorological regime. In the region of the Fiji Islands several boundary layer samples had SO₂, DMS, and CS₂. In 1989, additional SO₂ measurements were made between Hawaii and the equator and to the west of Hawaii downwind of the Kilauea volcano plumes.Paper submitted to the 7th International Symposium of the Commission for Atmospheric Chemistry and Global Pollution on the Chemistry of the Global Atmosphere held in Chamrousse, France, from 5 to 11 September 1990.     

Estimation of effective roughness length for heat and momentum from FIFE data

Using aircraft and surface data from the 1987 FIFE experiment in Kansas, we estimate the roughness length for momentum to be 0.19 m (with an error range 0.10–0.35 m), and the ratio of roughness length for momentum to that for heat to be about 16 (with an error range of 7–35).     

Use of general circulation model output in the creation of climate change scenarios for impact analysis

Many scientific studies warn of a rapid global climate change during the next century. These changes are understood with much less certainty on a regional scale than on a global scale, but effects on ecosystems and society will occur at local and regional scales. Consequently, in order to study the true impacts of climate change, regional scenarios of future climate are needed. One of the most important sources of information for creating scenarios is the output from general circulation models (GCMs) of the climate system. However, current state-of-the-art GCMs are unable to simulate accurately even the current seasonal cycle of climate on a regional basis. Thus the simple technique of adding the difference between 2 × CO₂ and 1 × CO₂ GCM simulations to current climatic time series cannot produce scenarios with appropriate spatial and temporal details without corrections for model deficiencies. In this study a technique is developed to allow the information from GCM simulations to be used, while accommodating for the deficiencies. GCM output is combined with knowledge of the regional climate to produce scenarios of the equilibrium climate response to a doubling of the atmospheric CO₂ concentration for three case study regions, China, Sub-Saharan Africa and Venezuela, for use in biological effects models. By combining the general climate change calculated with several GCMs with the observed patterns of interannual climate variability, reasonable scenarios of temperature and precipitation variations can be created. Generalizations of this procedure to other regions of the world are discussed.     

Observations concerning the nature of maceral fluorescence alteration with time

Distinctive features of the alteration of maceral fluorescence intensity with upon blue-light or UV excitation are related to the level of organic maturation. Alteration has been measured in different media; the results demonstrate clearly that the negative component of the alteration phenomenon is due to photochemical oxidation. Highly weathered bituminous coals do not display negative alteration because the potential for oxidation quenching has been reduced. The positive component of alteration is thought to be due to the creation of additional absorption centers and increased molecular rigidity as a result of photochemical oxidation and the enhancement of cross-linking among mobile phase and network molecules.     

Cretaceous and Eocene lignite deposits, Jackson Purchase, Kentucky

Lignites occur in the Cretaceous McNairy Formation and the Eocene Claiborne Formation in the Jackson Purchase region of western Kentucky. The lone Cretaceous lignite sample has over 18 percent inertodetrinite and 32 percent humodetrinite which, along with the abundant mineral matter, suggests a possible allochthonous origin for the deposit. The Claiborne Formation lignites have higher humic maceral contents than the Cretaceous lignites. Palynology suggests that there was considerable variation in the plant communities responsible for the Claiborne deposits. Differences in the preservation of the various plants is also seen in the variations between the humic types, particularly in the ulminite and humodetrinite contents. Potter and Dilcher (1980) suggested that the Claiborne lignites in the Jackson Purchase and west Tennessee developed in the abandoned oxbows of Eocene rivers. Significant short-distance changes in the peat thickness, flora, and other depositional elements should be expected in such an environment and could easily account for the observed variations in composition.     

ALH85085: a unique volatile-poor carbonaceous chondrite with possible implications for nebular fractionation processes

Allan Hills 85085 is a unique chondrite with affinities to the Al Rais-Renazzo clan of carbonaceous chondrites. Its constituents are less than 50 μm in mean size. Chondrules and microchondrules of all textures are present; nonporphyritic chondrules are unusually abundant. The mean compositions of porphyritic, nonporphyritic and barred olivine chondrules resemble those in ordinary chondrites except that they are depleted in volatile elements. Ca-, Al-rich inclusions are abundant and largely free of nebular alteration; they comprise types similar to those in CM and CO chondrites, as well as unique types. Calcium dialuminate occurs in several inclusions. Metal, silicate and sulfide compositions are close to those in CM-CO chondrites and Al Rais and Renazzo. C1-chondrite clasts and metal-rich “reduced” clasts are present, but opaque matrix is absent. Siderophile abundances in ALH85085 are extremely high (e.g., Fe/Si= 1.7 × solar), and volatiles are depleted (e.g., Na/Si= 0.25 × solar, S/Si= 0.03 × solar). Nonvolatile lithophile abundances are similar to those in Al Rais, Renazzo, and CM and CO chondrites.ALH85085 agglomerated when temperatures in the nebula were near 1000 K, in the same region where Renazzo, Al Rais and the CI chondrites formed. Agglomeration of high-temperature material may thus be a mechanism by which the fractionation of refractory lithophiles occurred in the nebula. Chondrule formation must have occurred at high temperatures when clumps of precursors were small. After agglomeration, ALH85085 was annealed and lightly shocked. C1 and other clasts were subsequently incorporated during late-stage brecciation.     

Comparison of industrial and high-resolution thermal data in a sedimentary basin

Temperature, temperature gradient and heat flow, derived from four wells in the Western Canada Sedimentary Basin have been compared with similar quantities derived from maps constructed from industrial data. Individual industrial temperature data may differ from the high-resolution temperature log by up to 30 K, but linear regression of the collected data agrees within 10 K at all points observed. Some evidence suggests that measured conductivities, using drill-cuttings, are biased toward average values. Derived heat flows show agreement of heat flow within 10% within the Mesozoic section. In the Paleozoic section differences are greater, and more varied, with insufficient data for general conclusions. Both styles of measurement provide opportunities for interpretation, each contributing to thermal analysis of sedimentary basins.     

Influence of Casing Materials on Trace-Level Chemicals in Well Water

Four well casing materials — polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), and stainless steel 304 (SS 304) and 316 (SS 316) — were examined to determine their suitability for monitoring inorganic and organic constituents in well water.
The inorganic study used a factorial design to test the effect of concentration of mixed metals (arsenic [As], chromium [Cr], lead [Pb], and cadmium [Cd]), pH, and organic carbon. Sample times were 0.5, 4, 8, 24, and 72 hours. Except for slow loss of Pb, PTFE well casings had no significant effect on the concentration of metals in solution. For the other casings, changes in analyte concentration often exceeded 10 percent in eight hours or less and, thus, could bias analyses of samples taken from wells constructed with these materials. Specifically, PVC casings sorbed Pb and leached Cd; SS 316 casings sorbed As and Pb and leached Cd; and SS 304 casings sorbed As, Cr, and Pb and leached Cd. Both stainless steel casing materials showed markedly poorer performance than the PVC casings.
The well casings were also tested for sorption/desorption of 10 organic substances from the following classes: chlorinated alkehes, chlorinated aromatics, nitroaromatics and nitramines. Sample times were 0, 1, 8, 24, and 72 hours, seven days, and six weeks. There were no detectable losses of analytes in any of the sample solutions containing stainless steel well casings. Significant loss of some analytes was observed in sample solutions containing plastic casings, although losses were always more rapid with the PTFE casings than with PVC. Chlorinated organic substances were lost most rapidly. For samples containing PTFE casings, losses of some of these compounds were rapid enough (>10 percent in eight hours) to be of concern for ground water monitoring. Losses of hydrophobic organic constituents in samples containing PTFE casings were correlated with the compound's octanol/water partition coefficient.