Determination of Horizontal Aquifer Anisotropy with Three Wells

Existing methods for the determination of horizontal aquifer anisotropy by means of pumping tests require a minimum of four wells, one for water withdrawal and three for drawdown observations. This paper shows how the same methods can be used to determine anisotropy with as few as three wells, if at least two of them can be pumped in sequence. A field example is included. A method of analyzing data from more wells than the above minimum, by least squares, is also described.     

Advancing the understanding of variations of Arctic sea ice optical and thermal behaviors through an international research and mobility project

In recent decades, significant changes of Arctic sea ice have taken place. These changes are expected to influence the surface energy balance of the ice-covered Arctic Ocean. To quantify this energy ba...     

An assessment of uncertainties in VS profiles obtained from microtremor observations in the phased 2018 COSMOS blind trials

Journal of Seismology - Site response is a critical consideration when assessing earthquake hazards. Site characterization is key to understanding site effects as influenced by seismic site...     

“All the World's a Stage”: A GIS Framework for Recreating Personal Time‐Space from Qualitative and Quantitative Sources

This article presents a methodological model for the study of the space‐time patterns of everyday life. The framework utilizes a wide range of qualitative and quantitative sources to create two environmental stages, social and built, which place and contextualize the daily mobilities of individuals as they traverse urban environments. Additionally, this study outlines a procedure to fully integrate narrative sources in a GIS. By placing qualitative sources, such as narratives, within a stage‐based GIS, researchers can begin to tell rich spatial stories about the lived experiences of segregation, social interaction, and environmental exposure. The article concludes with a case study utilizing the diary of a postal clerk to outline the wide applicability of this model for space‐time GIS research.     

Liquidus Equilibria in the System K2O-Na2O-Al2O3-SiO2-F2O-1-H2O to 100 MPa: I. Silicate-Fluoride Liquid Immiscibility in Anhydrous Systems

Liquidus relations in the four-component system Na₂O–Al₂O₃–SiO₂–F₂O_–1were studied at 0· 1 and 100 MPa to define the locationof fluoride–silicate liquid immiscibility and outlinedifferentiation paths of fluorine-bearing silicic magmas. Thefluoride–silicate liquid immiscibility spans the silica–albite–cryoliteand silica–topaz–cryolite ternaries and the haplogranite-cryolitebinary at greater than 960°C and 0· 1–100 MPa.With increasing Al₂O₃ in the system and increasing aluminum/alkalication ratio, the two-liquid gap contracts and migrates fromthe silica liquidus to the cryolite liquidus. The gap does notextend to subaluminous and peraluminous melt compositions. Forall alkali feldspar–quartz-bearing systems, the miscibilitygap remains located on the cryolite liquidus and is thus inaccessibleto differentiating granitic and rhyolitic melts. In peralkalinesystems, the magmatic differentiation is terminated at the albite–quartz–cryoliteeutectic at 770°C, 100 MPa, 5 wt % F and cation Al/Na =0· 75. The addition of topaz, however, significantlylowers melting temperatures and allows strong fluorine enrichmentin subaluminous compositions. At 100 MPa, the binary topaz–cryoliteeutectic is located at 770°C, 39 wt % F, cation Al/Na 0·95, and the ternary quartz–topaz–cryolite eutecticis found at 740°C, 32 wt % F, 30 wt % SiO₂ and cation Al/Na 0· 95. Such location of both eutectics enables fractionationpaths of subaluminous quartz-saturated systems to produce fluorine-rich,SiO₂-depleted and nepheline-normative residual liquids. KEY WORDS: silicate melt; granite; rhyolite; fluorine; liquid immiscibility     

The evolution of He Isotopes in the convecting mantle and the preservation of high He/He ratios

A key requirement for any model of mantle evolution is accounting for the high ³He/⁴He ratios of many ocean island basalts compared to those of mid-ocean ridge basalts. The early, popular paradigm of primitive, undegassed mantle stored in a convectively isolated lower mantle is incompatible with geophysical constraints that imply whole mantle convection. Thus it has been suggested more recently that domains with high ³He/U ratios have been created continuously from the bulk mantle throughout Earth history. Such models require that the ³He/⁴He ratio of the convecting mantle was at least as high as the highest values seen in OIB at the time the OIB source was generated. These domains must also be created with sufficient He to impart distinctive He isotopic signatures to ocean island basalts. However, the He isotope evolution of the mantle has not been consistently quantified to determine if such scenarios are plausible.

Here a simple model of the He evolution of the whole mantle is examined. Using a wide range of possible histories of continental extraction and He degassing, the bulk convecting mantle was found to have had ³He/⁴He ratios as high as those seen in the Iceland hotspot only prior to 3 Ga. Such high ³He/⁴He ratios can only be preserved if located in domains that are not modified by convective mixing or diffusive homogenisation since that time. Further, there are difficulties in producing, with commonly invoked magmatic processes, domains with sufficiently high ³He/U ratios and enough ³He to be able to impart this signature to ocean island basalts. The results are consistent with models that store such He signatures in the core or a deep layer in the mantle, but are hard to reconcile with models that continuously generate high ³He/⁴He domains within the mantle.     

The imprint of basalt on the geochemistry of silicic magmas

We propose that the fluid mechanics of magma chamber replenishment leads to a novel process whereby silicic magmas can acquire an important part of their chemical signatures. When flows of basaltic magma enter silicic magma chambers, they assume a ‘fingered' morphology that creates a large surface area of contact between the two magmas. This large surface area provides an opportunity for significant chemical exchange between the magmas by diffusion that is enhanced by continuous flow of silicic liquid traversing the basalt through thin veins. A quantitative analysis shows that a basaltic magma may thereby impart its trace-element and isotopic characteristics to a silicic magma. Depending on concentration differences and diffusion coefficients for the given components, this new mechanism may be as important as crystal fractionation and assimilation in producing the compositional diversity of silicic magmas. It may explain concentration gradients in silicic ash-flow tuffs and should be considered when interpreting the isotopic signatures of silicic rocks, even in the overt absence of mixing. For example, we show that, for several well studied, compositionally graded ash-flow tuffs, the concentrations and isotopic ratios of important geochemical tracers such as strontium could be largely due to this flow-enhanced diffusion process.