The space-time cube as part of a GeoVisual analytics environment to support the understanding of movement data

This paper reports the results of an empirical usability experiment on the performance of the space-time cube in a GeoVisual analytics environment. It was developed to explore movement data based on the requirements of human geographers. The interactive environment consists of multiple coordinated views incorporating three graphical representations. For the experiment, two groups of the user, domain experts and non-domain experts, had to execute several map-use tasks to answers specific question. The data collected during the experiment were analysis resulting in a set of usability metrics related to the effectiveness, efficiency and user satisfaction of developed application. The comparison of both groups showed that domain experts were able to operate the visual analytical environment more effectively and efficiently due to their interest to explore their data. The user feedback derived from the analysis of both experiments was further processed for the improvement of the application.     

Zircon geochronology and geochemistry to constrain the youngest eruption events and magma evolution of the Mid-Miocene ignimbrite flare-up in the Pannonian Basin,eastern central Europe

A silicic ignimbrite flare-up episode occurred in the Pannonian Basin during the Miocene, coeval with the syn-extensional period in the region. It produced important correlation horizons in the regional stratigraphy; however, they lacked precise and accurate geochronology. Here, we used U–Pb (LA-ICP-MS and ID-TIMS) and (U–Th)/He dating of zircons to determine the eruption ages of the youngest stage of this volcanic activity and constrain the longevity of the magma storage in crustal reservoirs. Reliability of the U–Pb data is supported by (U–Th)/He zircon dating and magnetostratigraphic constraints. We distinguish four eruptive phases from 15.9 ± 0.3 to 14.1 ± 0.3 Ma, each of which possibly includes multiple eruptive events. Among these, at least two large volume eruptions (>10 km³) occurred at 14.8 ± 0.3 Ma (Demjén ignimbrite) and 14.1 ± 0.3 Ma (Harsány ignimbrite). The in situ U–Pb zircon dating shows wide age ranges (up to 700 kyr) in most of the crystal-poor pyroclastic units, containing few to no xenocrysts, which implies efficient recycling of antecrysts. We propose that long-lived silicic magma reservoirs, mostly kept as high-crystallinity mushes, have existed in the Pannonian Basin during the 16–14 Ma period. Small but significant differences in zircon, bulk rock and glass shard composition among units suggest the presence of spatially separated reservoirs, sometimes existing contemporaneously. Our results also better constrain the time frame of the main tectonic events that occurred in the Northern Pannonian Basin: We refined the upper temporal boundary (15 Ma) of the youngest counterclockwise block rotation and the beginning of a new deformation phase, which structurally characterized the onset of the youngest volcanic and sedimentary phase.     

New insights into geochemical behaviour in ancient marine carbonates (Upper Jurassic Ammonitico Rosso): Novel proxies for interpreting sea‐level dynamics and palaeoceanography

Elemental concentrations in Phanerozoic sea water are known to fluctuate both in time and space. With regard to carbonates precipitated from marine fluids, elemental concentrations in the carbonate crystal lattice are affected by a complex array of equilibrium and non‐equilibrium as well as post‐depositional alteration processes. To assess the potential of carbonate elemental chemostratigraphy, seven Upper Jurassic sections were investigated along a proximal to distal transect across the south‐east Iberian palaeomargin. The aim was to explore stratigraphic and spatial variations in calcium, strontium, magnesium, iron and manganese elemental abundances. The epicontinental geochemical record is influenced by the combination of continental runoff and a significant diagenetic overprint. In contrast, the epioceanic geochemical record agrees with reconstructed open marine sea water values, reflecting a moderate degree of syn‐depositional to early marine pore water diagenesis. Establishing a fair degree of preservation of matrix micrite, a thorough statistical approach was applied and elemental associations tested for their environmental significance. Principal component and hierarchical cluster analyses revealed a persistent relation between carbonate magnesium, iron and strontium abundances. Processes related to early diagenetic nodulation in Ammonitico Rosso facies most probably account for the incorporation of these elements in the calcium carbonate lattice. The clear decoupling of carbonate manganese abundance with respect to the remaining elements is documented and related to high sea floor spreading rates and hydrothermal activity during the Late Jurassic. The investigation of potential time‐fluctuation of geochemical patterns was approached through variogram computation. The observed temporal behaviour is most likely to be forced by relative sea‐level dynamics, reflecting Late Jurassic palaeoceanographic conditions and potential planetary interactions. The data obtained in this study highlight the utility of elemental data from carbonate matrix micrites as geochemical proxies for studying the influence of remote trigger factors.     

Mendigite,Mn2Mn2MnCa(Si3O9)2, a new mineral species of the bustamite group from the Eifel volcanic region,Germany

A new mineral, mendigite (IMA no. 2014-007), isostructural with bustamite, has been found in the In den Dellen pumice quarry near Mendig, Laacher Lake area, Eifel Mountains, Rhineland-Palatinate (Rheinland-Pfalz), Germany. Associated minerals are sanidine, nosean, rhodonite, tephroite, magnetite, and a pyrochlore-group mineral. Mendigite occurs as clusters of long-prismatic crystals (up to 0.1 × 0.2 × 2.5 mm in size) in cavities within sanidinite. The color is dark brown with a brown streak. Perfect cleavage is parallel to (001). D _calc = 3.56 g/cm³. The IR spectrum shows the absence of H₂O and OH groups. Mendigite is biaxial (–), α = 1.722 (calc), β = 1.782(5), γ = 1.796(5), 2V _meas = 50(10)°. The chemical composition (electron microprobe, mean of 4 point analyses, the Mn²⁺/Mn³⁺ ratio determined from structural data and charge-balance constraints) is as follows (wt %): 0.36 MgO, 10.78 CaO, 37.47 MnO, 2.91 Mn₂O₃, 4.42 Fe₂O₃, 1.08 Al₂O₃, 43.80 SiO₂, total 100.82. The empirical formula is Mn_2.00(Mn_1.33Ca_0.67) (Mn_0.50 ²⁺ Mn_0.28 ³⁺ Fe_0.15 ³⁺ Mg_0.07)(Ca_0.80 (Mn_0.20 ²⁺)(Si_5.57 Fe_0.27 ³⁺ Al_0.16O₁₈). The idealized formula is Mn₂Mn₂MnCa(Si₃O₉)₂. The crystal structure has been refined for a single crystal. Mendigite is triclinic, space group \(P\bar 1\); the unit-cell parameters are a = 7.0993(4), b = 7.6370(5), c = 7.7037(4) Å, α = 79.58(1)°, β = 62.62(1)°, γ = 76.47(1)°; V = 359.29(4) ų, Z = 1. The strongest reflections on the X-ray powder diffraction pattern [d, Å (I, %) (hkl)] are: 3.72 (32) (020), 3.40 (20) (002, 021), 3.199 (25) (012), 3.000 (26), (\(01\bar 2\), \(1\bar 20\)), 2.885 (100) (221, \(2\bar 11\), \(1\bar 21\)), 2.691 (21) (222, \(2\bar 10\)), 2.397 (21) (\(02\bar 2\), \(21\bar 1\), 203, 031), 1.774 (37) (412, \(3\bar 21\)). The type specimen is deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, registration number 4420/1.