Oxygen Isotope Variations of Basaltic Lavas and Upper Mantle Rocks

This chapter summarizes the oxygen isotope geochemistry of terrestrial basalts and their mantle sources, including the conceptual framework for interpreting such data and the phenomenology of known variations. In particular, the first section outlines the motivations for and first-order results of oxygen isotope studies of terrestrial and lunar basalts over the last 30 years; the second section reviews oxygen isotopic fractionations among phases relevant for studying basalts and mantle rocks; the third summarizes variations in δ^(18)O of various crustal rocks that may contribute to the petrogenesis of basalts either as subducted source components or lithospheric contaminants; and the final and longest section describes observed oxygen isotope variations of major classes of terrestrial basalts and related mantle nodules with an emphasis on data generated within the last six years using laser-based fluorination techniques. In the interests of brevity, I do not describe in detail methods for oxygen isotope analysis or changes in δ^(18)O of volcanic rocks caused by sub-solidus alteration; however, these issues are important practical considerations for anyone studying oxygen isotope compositions of basalts and interested readers are directed to the following references: analytical methods: Sharp (1990), Mattey and Macpherson (1993), and Valley et al. (1995); basalt alteration: Muehlenbachs (1986), Alt (1993), and Staudigel et al. (1995)

Absolute Moments of Generalized Hyperbolic Distributions and Approximate Scaling of Normal Inverse Gaussian Lévy-Processes

Expressions for (absolute) moments of generalized hyperbolic (GH) and normal inverse Gaussian (NIG) laws are given in terms of moments of the corresponding symmetric laws. For the (absolute) moments centered at the location parameter mu explicit expressions as series containing Bessel functions are provided. Furthermore the derivatives of the logarithms of (absolute) mu-centered moments with respect to the logarithm of time are calculated explicitly for NIG Levy processes. Computer implementation of the formulae obtained is briefly discussed. Finally some further insight into the apparent scaling behaviour of NIG Levy processes (previously discussed in Barndorff-Nielsen and Prause (2001)) is gained

Oxygen isotope geochemistry of the second HSDP core

Oxygen isotope ratios were measured in olivine phenocrysts (~1 mm diameter), olivine microphenocrysts (generally ~100–200 µm diameter), glass, and/or matrix from 89 samples collected from depths down to 3079.7 m in the second, and main, HSDP core (HSDP-2). Olivine phenocrysts from 11 samples from Mauna Loa and 34 samples from the submarine section of Mauna Kea volcano have delta18O values that are similar to one another (5.11 ± 0.10‰, 1sigma, for Mauna Loa; 5.01 ± 0.07‰, for submarine Mauna Kea) and within the range of values typical of olivines from oceanic basalts (delta18O of ~5.0 to 5.2‰). In contrast, delta18O values of olivine phenocrysts from 20 samples taken from the subaerial section of Mauna Kea volcano (278 to 1037 mbsl) average 4.79 ± 0.13‰. Microphenocrysts in both the subaerial (n = 2) and submarine (n = 24) sections of Mauna Kea are on average ~0.2‰ lower in delta18O than phenocrysts within the same stratigraphic interval; those in submarine Mauna Kea lavas have an average delta18O of 4.83 ± 0.11‰. Microphenocrysts in submarine Mauna Kea lavas and phencrysts in Mauna Loa lavas are the only population of olivines considered in this study that are typically in oxygen isotope exchange equilibrium with coexisting glass or groundmass. These data confirm the previous observation that the stratigraphic boundary between Mauna Loa and Mauna Kea lavas defines a shift from “normal” to unusually low delta18O values. Significantly, they also document that the distinctive 18O-depleted character of subaerial Mauna Kea lavas is absent in phenocrysts of submarine Mauna Kea lavas. Several lines of evidence suggest that little if any of the observed variations in delta18O can be attributed to subsolidus alteration or equilibrium fractionations accompanying partial melting or crystallization. Instead, they reflect variable proportions of an 18O-depleted source component or contaminant from the lithosphere and/or volcanic edifice that is absent in or only a trace constituent of subaerial Mauna Loa lavas, a minor component of submarine Mauna Kea lavas, and a major component of subaerial Mauna Kea lavas. Relationships between the delta18O of phenocrysts, microphenocrysts, and glass or groundmass indicate that this component (when present) was added over the course of crystallization-differentiation. This process must have taken place in the lithosphere and most likely at depths of between ~5 and 15 km. We conclude that the low-delta18O component is either a contaminant from the volcanic edifice that was sampled in increasingly greater proportions as the volcano drifted off the center of the Hawaiian plume or a partial melt of low-delta18O, hydrothermally altered perdotites in the shallow Pacific lithosphere that increasingly contributed to Mauna Kea lavas near end of the volcano's shield building stage. The first of these alternatives is favored by the difference in delta18O between subaerial and submarine Mauna Kea lavas, whereas the second is favored by systematic differences in radiogenic and trace element composition between higher and lower delta18O lavas

Oxygen isotope ratios in olivine from the Hawaii Scientific Drilling Project

Oxygen isotope ratios of olivine in 23 tholeiites from the Hawaii Scientific Drilling Project (HSDP) core (15 from Mauna Kea, 8 from Mauna Loa) and three samples of outcropping subaerial or dredged submarine Mauna Kea lavas have been measured by laser fluorination. The δ^(18)O values are 4.6–5.4 ‰, confirming previous observations that some Hawaiian lavas are derived from sources with δ^(18)O values lower than typical upper mantle (δ^(18)Oolivine ≈ 5.2±0.2 ‰). The Mauna Kea-Mauna Loa transition marks a shift from δ^(18)O values lower than the mantle average in Mauna Kea olivines (∼4.8) to more typical mantle values in Mauna Loa olivines. Lavas containing olivines with δ^(18)O values similar to the typical upper mantle are associated with more “primitive” or less depleted radiogenic isotope characteristics; i.e., with higher ^3He/^4He (>13 Ra), higher ^(87)Sr/^(86)Sr (>0.7036) and lower є_(Nd) (<6.5), and with ^(206)Pb/^(204)Pb ratios less than -18.3. These relationships indicate that the δ^(18)O values of the relatively enriched source components of the Hawaiian plume sampled by Mauna Loa lavas are comparable to (or greater than) the mantle average. This conclusion is supported by δ^(18)O values of olivine from other high ^3He/^4He islands, which are also comparable to the upper mantle average. The low δ^(18)O values in Hawaiian lavas are derived from a source having more MORB-like, or depleted, He, Nd, and Sr isotope ratios, but more radiogenic Pb than is seen in the Mauna Loa lavas Assimilation of ^(18)O-depleted lower oceanic crust from the underlying Pacific crust by hot, MgO-rich parental magmas or melting of older, recycled oceanic crust entrained in the Hawaiian plume are both possible sources of this ^(18)O-depleted, MORB-like component in Hawaiian magmas

Accretion and Preservation of D-rich Organic Particles in Carbonaceous Chondrites: Evidence for Important Transport in the Early Solar System Nebula

We have acquired NanoSIMS images of the matrices of CI, CM, and CR carbonaceous chondrites to study, in situ, the organic matter trapped during the formation of their parent bodies. D/H ratio images reveal the occurrence of D-rich hot spots, constituting isolated organic particles. Not all the organic particles are D-rich hot spots, indicating that at least two kinds of organic particles have been accreted in the parent bodies. Ratio profiles through D-rich hot spots indicate that no significant self-diffusion of deuterium occurs between the D-rich organic matter and the depleted hydrous minerals that are surrounding them. This is not the result of a physical shielding by any constituent of the chondrites. Ab initio calculations indicate that it cannot be explained by isotopic equilibrium. Then it appears that the organic matter that is extremely enriched in D does not exchange with the hydrous minerals, or this exchange is so slow that it is not significant over the 4.5 billion year history on the parent body. If we consider that the D-rich hot spots are the result of an exposure to intense irradiation, then it appears that carbonaceous chondrites accreted organic particles that have been brought to different regions of the solar nebula. This is likely the result of important radial and vertical transport in the early solar system

Design and Implementation of a Generic Framework for Rule-based Automated User Role Management

Many systems that host groups of users, like social media platforms, provide solutions or tools for users and groups of users. Within these groups, there can exist roles, which again might be connected to permissions. The role model itself can vary from system to system. Some are hierarchical, some have flat hierarchies, some are related to the permissions, others with notifications. Decoupling the role model implementation from the rest of the system has multiple advantages, such as achieving automatic role assignment more easily and being able to change a role model on the fly. Within this master thesis, challenges of automated role assignment are examined and necessary elements for how a development tool can help are distilled. The main contribution is the tool karmantra, which allows to integrate arbitrary role models in software projects and lets developers extend or alter them. The tool is kept in a very generic way to be expandable easily. With this tool, a step is taken towards decoupled and transparent role systems, that can not only serve the needs of common commercial platform needs