Insights into mantle-type volatiles contribution from dissolved gases in artesian waters of the Great Artesian Basin, Australia

The geochemical features of the volatiles dissolved in artesian thermal waters discharged over three basins (Millungera, Galilee and Cooper basin) of the Australian Great Artesian Basin (GAB) consistently indicate the presence of fluids from multiple gas sources located in the crust (e.g. sediments, oil reservoirs, granites) as well as minor but detectable contributions of mantle/magma-derived fluids. The gases extracted from 19 water samples and analyzed for their chemical and isotopic composition exhibit amounts of CO up to about 340mlSTP/L marked by a δC (Total Dissolved Carbon) ranging from -16.9 to +0.18‰ vs PDB, while CH concentrations vary from 4.4×10 to 4.9mlSTP/L. Helium contents were between 9 and >2800 times higher than equilibrium with Air Saturated Water (ASW), with a maximum value of 0.12mlSTP/L. Helium isotopic composition was in the 0.02-0.21 Ra range (Ra = air-normalized He/He ratio). The three investigated basins differ from each other in terms of both chemical composition and isotopic signatures of the dissolved gases whose origin is attributed to both mantle and crustal volatiles. Mantle He is present in the west-central and hottest part of the GAB despite no evidence of recent volcanism. We found that the partial pressure of helium, significantly higher in crustal fluids than in mantle-type volatiles, enhances the crustal He signature in the dissolved gases, thus masking the original mantle contribution. Neotectonic activity involving deep lithospheric structures and magma intrusions, highlighted by recent geophysical investigations, is considered to be the drivers of mantle/magmatic volatiles towards the surface. The results, although pertaining to artesian waters from a vast area of >542,000km, provide new constraints on volatile injection, and show that fluids' geochemistry can provide additional and independent information on the geo-tectonic settings of the Great Artesian Basin and its geothermal potential

La disclosure volontaria del modello di business nel prospetto informativo di quotazione: un’analisi comparative

How do companies to be listed actually deal with voluntary disclosure of their business model? Is it true that firms with greater knowledge-based resources and technological innovation endowments have a lower propensity to adopt fully open communication behaviors? This paper aims to identify the voluntary disclosure policies adopted by three Italian companies in their Initial Public Offering (IPO) prospectuses in order to investigate whether any differences may depend on the type of innovation underlying each business model. A series of interviews conducted with the top management made it possible to understand more deeply the business model of each company. Further, a content analysis has been developed to compute a measure of disclosure and to point out the strategic concepts and their relevance. We provide evidence that companies with a business model based on technology-push innovation have a lower propensity to the full disclosure of their intangible components, particularly of those mainly based on knowledge as these are also invisible. Our study adds to the literature of business and financial reporting by focusing on a new object of inquiry, that is the business model. The business model plays an important role in allowing external actors to understand a company’s value, thus companies’ strategic communication should be shaped accordingly. The results suggest the need to address the issue of voluntary disclosure of the business model by first distinguishing “visible” intangible resources from those that are “invisible” (both to financial and competitive markets). The study aims to make a contribution to the ongoing debate on business and financial reporting practice

Effectiveness of arsenic co-precipitation with Fe-Al hydroxides for treatment of contaminated water.

The purpose of this study was to assess the effectiveness of Al-Fe (hydr)oxide co-precipitates for the removal of As from wastewater and to assess the chemical stability of the products

Al-rich spinel in primitive arc volcanics

Al-rich spinels (100Cr/(Cr + Al) 50 wt%) are common in alpine peridotites, both terrestrial and lunar mafic and ultramafic cumulates, and in certain metamorphic rocks, but they are apparently rare in terrestrial volcanic rocks. Here we describe the occurrence of Al-rich spinel inclusions in olivine phenocrysts in island are volcanic rocks from five new localities: Bukit Mapas (Sumatra) and eastern Ball in the Sunda are, and Epi, Merelava, and Ambrym islands in the Vanuatu are. More commonly, relatively Cr-rich spinels also occur as inclusions in the same olivine phenocrysts, and it appears that the Cr-poor aluminous spinels must be in disequilibrium with the host basaltic melts. In the rocks studied, Al-rich spinels also coexist with trapped silicate glasses and highly aluminous clinopyroxene in melt inclusions in olivine. This paragenesis suggests an origin involving contamination by localised Al-rich melt pockets as opposed to a xenocrystic origin. Two mechanisms to produce this high-Al melt in basaltic magma chambers are suggested: (1) localized high-Al melt production by complete breakdown of assimilated lower crustal gabbroic rocks. In this model the high-Al melt may crystallise Al-rich spinels which are subsequently trapped as solid inclusions by phenocryst phases of the host basaltic melt or may be trapped as melt inclusions in which Al-rich spinels and Al-rich clinopyroxene crystallise as daughter phases, and (2) incongruent breakdown of amphibole in amphibole-rich cumulates in sub-are, or sub-GIB volcano magma chambers. The latter reaction produces a melt with similar to 20-22% of Al2O3, aluminous clinopyroxene, Al-rich spinel and olivine. Mixing between these amphibole breakdown products and host basaltic melt may occur throughout the evolution of a magmatic system, but particularly during recharge with hot magnesian basalt batches. Aluminous spinels and aluminous clinopyroxene produced during amphibole breakdown, or perhaps crystallised from aluminous melt produced in the same reaction, are incorporated into the magma during recharge, and subsequently trapped, together with the coexisting Cr-spinels, by crystallising olivine and clinopyroxene

Low arsenic bioaccessibility by fixation in nanostructured iron (Hydr)oxides: quantitative identification of As-bearing phases

A new analytical protocol was developed to provide quantitative, single-particle identification of arsenic in heterogeneous nanoscale mineral phases in soil samples, with a view to establishing its potential risk to human health. Microscopic techniques enabled quantitative, single-particle identification of As-bearing phases in twenty soil samples collected in a gold mining district with arsenic concentrations in range of 8 to 6354 mg kg. Arsenic is primarily observed in association with iron (hydr) oxides in fine intergrowth with phyllosilicates. Only small quantities of arsenopyrite and ferric arsenate (likely scorodite) particles, common in the local gold mineralization, were identified (e.g., 7 and 9 out, respectively, of app. 74,000 particles analyzed). Within the high-arsenic subgroup, the arsenic concentrations in the particle size fraction below 250μm ranges from 211 to 4304 mg kg. The bioaccessible arsenic in the same size fraction is within 0.86–22 mg kg (0.3–5.0%). Arsenic is trapped in oriented aggregates of crystalline iron (hydr)oxides nanoparticles, and this mechanism accounts for the low As bioaccessibility. The calculated As exposure from soil ingestion is less than 10% of the arsenic Benchmark Dose Lower Limit - BMDL. Therefore, the health risk associated with the ingestion of this geogenic material is considered to be low

Post-supereruption recovery at Toba Caldera

Large calderas, or supervolcanoes, are sites of the most catastrophic and hazardous events on Earth, yet the temporal details of post-supereruption activity, or resurgence, remain largely unknown, limiting our ability to understand how supervolcanoes work and address their hazards. Toba Caldera, Indonesia, caused the greatest volcanic catastrophe of the last 100 kyr, climactically erupting ~74 ka. Since the supereruption, Toba has been in a state of resurgence but its magmatic and uplift history has remained unclear. Here we reveal that new 14 C, zircon U-Th crystallization and (U-Th)/He ages show resurgence commenced at 69.7±4.5 ka and continued until at least ~2.7 ka, progressing westward across the caldera, as reflected by post-caldera effusive lava eruptions and uplifted lake sediment. The major stratovolcano north of Toba, Sinabung, shows strong geochemical kinship with Toba, and zircons from recent eruption products suggest Toba's climactic magma reservoir extends beneath Sinabung and is being tapped during eruptions