The effects of metamorphism on O and Fe isotope compositions in the Biwabik Iron Formation, northern Minnesota

The Biwabik Iron Formation of Minnesota (1.9 Ga) underwent contact metamorphism by intrusion of the Duluth Complex (1.1 Ga). Apparent quartz–magnetite oxygen isotope temperatures decrease from ∼700°C at the contact to ∼375°C at 2.6 km distance (normal to the contact in 3D). Metamorphic pigeonite at the contact, however, indicates that peak temperatures were greater than 825°C. The apparent O isotope temperatures, therefore, reflect cooling, and not peak metamorphic conditions. Magnetite was reset in δ¹⁸O as a function of grain size, indicating that isotopic exchange was controlled by diffusion of oxygen in magnetite for samples from above the grunerite isograd. Apparent quartz–magnetite O isotope temperatures are similar to calculated closure temperatures for oxygen diffusion in magnetite at a cooling rate of ∼5.6°C/kyr, which suggests that the Biwabik Iron Formation cooled from ∼825 to 400°C in ∼75 kyr at the contact with the Duluth Complex. Isotopic exchange during metamorphism also occurred for Fe, where magnetite–Fe silicate fractionations decrease with increasing metamorphic grade. Correlations between quartz–magnetite O isotope fractionations and magnetite–iron silicate Fe isotope fractionations suggest that both reflect cooling, where the closure temperature for Fe was higher than for O. The net effect of metamorphism on δ¹⁸O–δ⁵⁶Fe variations in magnetite is a strong increase in δ¹⁸O_Mt and a mild decrease in δ⁵⁶Fe with increasing metamorphic grade, relative to the isotopic compositions that are expected at the low temperatures of initial magnetite formation. If metamorphism of Iron Formations occurs in a closed system, bulk O and Fe isotope compositions may be preserved, although re-equilibration among the minerals may occur for both O and Fe isotopes. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Projected changes in meteorological drought over East Africa inferred from bias-adjusted CMIP6 models

Natural Hazards - The ongoing global warming has caused unprecedented changes in the climate system, leading to an increase in the intensity and frequency of weather and climate extremes. This...     

基于傅里叶变换质谱的烃源岩成熟度评价方法及地质意义

<正>伴随非常规油气资源的勘探开发,油气资源开采的广度和深度进一步扩大,一定程度上缓解了我国油气供需矛盾、保障了我国能源安全,同时有力推动了能源结构战略转型。但同时也对能源地质研究工作提出了新的挑战。有机质成熟度是油气评价的重要参数之一,不同成熟阶段的有机质会对应产出不同成因、不同性质、不同质量的油气,如何准确评价沉积有机质成熟度是当前油气资源勘探开发工作的关键问题之一。前人在科研实践工作中从光学、化学、谱学等角度提出了适用条件各异的成熟度评价方法,在部分地质环境中获得了良好的应用效果,但已有的成熟度指标多受测定方法原理的制约导致其适用性不同程度受限(肖贤明等,2020),制约了油气资源的高质量勘探开发。     

The most frequent interfaces in olivine aggregates: the GBCD and its importance for grain boundary related processes

Rocks consist of crystal grains separated by grain boundaries that impact the bulk rock properties. Recent studies on metals and ceramics showed that the grain boundary plane orientation is more significant for grain boundary properties than other characteristics such as the sigma value or disorientation (in the Earth’s science community more frequently termed misorientation). We determined the grain boundary character distribution (GBCD) of synthetic and natural polycrystalline olivine, the most abundant mineral of Earth’s upper mantle. We show that grain boundaries of olivine preferentially contain low index planes, in agreement with recent findings on other oxides (e.g. MgO, TiO₂, Al₂O₃ etc.). Furthermore, we find evidence for a preferred orientation relationship of 90° disorientations about the [001] direction forming tilt and twist grain boundaries, as well as a preference for the 60° disorientation about the [100] axis. Our data indicate that the GBCD, which is an intrinsic property of any mineral aggregate, is fundamental for understanding and predicting grain boundary related processes.     

Do sedentary behavior and physical activity spatially cluster? Analysis of a population-based sample of Boston adolescents

Sedentary behavior and lack of physical activity are key modifiable behavioral risk factors for chronic health problems, such as obesity and diabetes. Little is known about how sedentary behavior and physical activity among adolescents spatially cluster. The objective was to detect spatial clustering of sedentary behavior and physical activity among Boston adolescents. Data were used from the 2008 Boston Youth Survey Geospatial Dataset, a sample of public high school students who responded to a sedentary behavior and physical activity questionnaire. Four binary variables were created: (1) TV watching (>2 h/day), (2) video games (>2 h/day), (3) total screen time (>2 h/day); and (4) 20 min/day of physical activity (≥5 days/week). A spatial scan statistic was utilized to detect clustering of sedentary behavior and physical activity. One statistically significant cluster of TV watching emerged among Boston adolescents in the unadjusted model. Students inside the cluster were more than twice as likely to report >2 h/day of TV watching compared to respondents outside the cluster. No significant clusters of sedentary behavior and physical activity emerged. Findings suggest that TV watching is spatially clustered among Boston adolescents. Such findings may serve to inform public health policy-makers by identifying specific locations in Boston that could provide opportunities for policy intervention. Future research should examine what is linked to the clusters, such as neighborhood environments and network effects.     

The effect of species diversity on metal adsorption onto bacteria

In this study, we measure proton, Pb, and Cd adsorption onto the bacteria Deinococcus radiodurans, Thermus thermophilus, Acidiphlium angustum, Flavobacterium aquatile, and Flavobacterium hibernum, and we calculate the thermodynamic stability constants for the important surface complexes. These bacterial species represent a wide genetic diversity of bacteria, and they occupy a wide range of habitats. All of the species, except for A. angustum, exhibit similar proton and metal uptake. The only species tested that exhibits significantly different protonation behavior is A. angustum, an acidophile that grows at significantly lower pH than the other species of this study. We demonstrate that a single, metal-specific, surface complexation model can be used to reasonably account for the acid/base and metal adsorption behaviors of each species. We use a four discrete site non-electrostatic model to describe the protonation of the bacterial functional groups, with averaged pK_a values of 3.1 ± 0.3, 4.8 ± 0.2, 6.7 ± 0.1, and 9.2 ± 0.3, and site concentrations of (1.0 ± 0.17) × 10⁻⁴, (9.0 ± 3.0) × 10⁻⁵, (4.6 ± 1.8) × 10⁻⁵, and (6.1 ± 2.3) × 10⁻⁵ mol of sites per gram wet mass of bacteria, respectively. Adsorption of Cd and Pb onto the bacteria can be accounted for by the formation of complexes with each of the bacterial surface sites. The average log stability constants for Cd complexes with Sites 1-4 are 2.4 ± 0.4, 3.2 ± 0.1, 4.4 ± 0.1, and 5.3 ± 0.1, respectively. The average log stability constants for Pb complexes with Sites 1-4 are 3.3 ± 0.2, 4.5 ± 0.3, 6.5 ± 0.1, and 7.9 ± 0.5, respectively. This study demonstrates that a wide range of bacteria exhibit similar proton and metal adsorption behaviors, and that a single set of averaged acidity constants, site concentrations, and stability constants for metal-bacterial surface complexes yields a reasonable model for the adsorption behavior of many of these species. The differences in adsorption behavior that we observed for A. angustum demonstrate that genetic differences do exist between the cell wall functional group chemistries of some bacterial species, and that significant exceptions to the typical bacterial adsorption behavior do exist.     

The origin of large varioles in flow-banded pillow lava from the Hooggenoeg Complex,Barberton Greenstone Belt,South Africa

Exceptionally well-preserved pillowed and massive phenocryst-free metabasaltic lava flows in the uppermost part of the Palaeoarchaean Hooggenoeg Complex of the Barberton Greenstone Belt exhibit both flow banding and large leucocratic varioles. The flow banding is defined by blebs and bands of pale and dark green metabasalt and was the result of mingling of two types of basalt (Robins et al. in Bull Volcanol 72:579–592, 2010a). Varioles occur exclusively in the dark chlorite-, MgO- and FeO-rich metabasalt. Varioles are absent in the outermost rinds of pillows and increase in both abundance and size towards the centres of pillows. In the central parts of some pillows, they impinge to form homogeneous pale patches, bands or almost homogenous cores. Individual varioles consist essentially of radially orientated or outwardly branching dendritic crystals of albite. Many varioles exhibit concentric zones and finer-grained rims. Some varioles seem to have grown around tiny vesicles and vesicles appear to have been trapped in others between a core and a finer-grained rim. The matrix surrounding the ocelli contains acicular pseudomorphs of actinolite and chlorite after chain-like, skeletal Ca-rich pyroxenes that are partly overgrown by the margins of varioles. Varioles are enriched in the chemical constituents of feldspar but contain concentrations of immobile TiO₂, Cr, Zr and REE that are similar to the host metabasalts. The shape, distribution, texture and composition of the varioles exclude liquid immiscibility and support an origin by spherulitic crystallisation of plagioclase from severely undercooled basalt melt and glass. Nucleation of plagioclase was strongly inhibited and took place on vesicles, on the bases of drainage cavities and along early fractures. Eruption in deep water and retention of relatively high concentrations of volatiles in the melt may be the principal cause of spherulitic crystallisation in the interiors of pillows rather than only in their margins as in younger submarine flows.     

Maturation related changes in the distribution of ester bound fatty acids and alcohols in a coal series from the New Zealand Coal Band covering diagenetic to catagenetic coalification levels

A rank series of lignites and coals of low to moderate maturation levels (vitrinite reflectance (R₀): 0.27–0.8%) from the New Zealand Coal Band were investigated using alkaline ester cleavage experiments to reveal compositional changes of ester bound components (fatty acids and alcohols) during increasing maturation. Ester bound alcohols are found to be present in highest amounts in the very immature lignite samples (R₀: 0.27–0.29%), but show a rapid decrease during early diagenesis. Ester bound fatty acids also show an initial exponential decrease during diagenesis, but reveal an intermittent increase during early catagenesis before decreasing again during main catagenesis. This intermittent increase was related to the short chain fatty acids. To obtain a maturity related signal and to eliminate facies related scattering in the amounts of fatty acids in the coal samples, the carbon preference index of fatty acids (CPI_FA) parameter is introduced here. For the long chain fatty acids (C₂₀–C₃₂) originating from terrigenous plant debris, the CPI_FA decreases with increasing maturity, showing a strong maturation related signal. During diagenesis, the same trend can be observed for the short chain fatty acids, but the intermittent increase in the amounts of short chain fatty acids is also accompanied by high CPI_FA values. This indicates less altered organic biomass at this advanced maturation level and is in contrast to the mature CPI_FA signal of the long chain fatty acids of the same samples. One possible reason for this discrepancy could be extremely different amounts of short and long chain fatty acids in the original source organic matter of these samples. However, another intriguing explanation could be the incorporation of immature bacterial biomass from deep microbial communities containing C₁₆ and C₁₈ fatty acids as main cell membrane components. Deep microbial life might be stimulated at this interval by the increasing release of thermally generated potential substrates from the organic matrix during early catagenesis. In contrast to the fatty acids, the high amounts of alcohols in the immature lignite samples are also visible in the alkene distribution from the open system pyrolysis experiments of the organic matrix before and after saponification.     

Neogene and Quaternary coexisting in the geological time scale: The inclusive compromise

Removing the Tertiary and Quaternary Periods whilst conserving the Paleogene and Neogene Periods in The Geological Timescale 2004 caused a storm of protest. One response was to advocate restoring an enlarged Quaternary and consigning the Neogene to a minor role within the Tertiary. Amongst an array of practical, traditional, sentimental and anthropocentric reasons for this response, the one hard-core justification was that the rigidly nested hierarchy of the geological timescale must be preserved.The central objective of this paper is conserving the historically legitimate, Miocene-present, Neogene Period and System. There are two options for conserving the Quaternary concurrently with the Neogene: (i) an inclusive compromise in a flexible hierarchy, and (ii) an upgrading of Pliocene and Pleistocene divisions to the level of epoch.In the inclusive compromise there coexist alternative pathways through the hierarchical ranks. Thus geohistorians and biohistorians have two options for traversing the hierarchy from era to age, as in this example using the hierarchical positioning of the Calabrian Age and Stage:either Cenozoic [era]↔Neogene [period]↔Pleistocene [epoch]↔Calabrian [age],or Cenozoic [era]↔Quaternary [subera]↔Pleistocene [epoch]↔Calabrian [age].We reaffirm that the inclusive compromise is entirely viable. In so doing we (i) challenge the necessity of the rigidly nested hierarchy, which should be capable of a little flexibility; (ii) reject all analogies of the arbitrary and conventional chronostratigraphic hierarchy with three natural biological hierarchies; (iii) reaffirm the integrity of the Neogene extending to the present; and (iv) see no reason to doubt the harmonious coexistence of the two options preserving the Quaternary and Neogene traditions in an orderly working and stable time scale.In the alternative schema conserving the Neogene, divisions of the Pliocene and Pleistocene are upgraded, so that the Late Pleistocene, Early Pleistocene and Late Pliocene Epochs comprise the Quaternary Subperiod, itself equivalent to Late Neogene. The inflexibly nested hierarchy is preserved but the Tertiary is lost.