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The Salitre intrusion, which is subdivided into Salitre I and Salitre II. It was dated to ~86-82 Ma by Sonoki and Garda (1988). It is part of the Alto Paranaíba Igneous Province (APIP, Fig. 1) in Brazil. The APIP is one of the largest ultrapotassic/carbonatitic/kimberlitic provinces in the world. The intrusion consists of lamproites, carbonatites, and one lamprophyre, as well as various intrusive cumulitic rocks. These rocks include perovskite-phlogopite dunites, phlogopite-perovskite clinopyroxenites (salitrites, s.l.), phlogopitites, phoscorites, and perovskitites. These rocks are characterized by variable enrichment of olivine, clinopyroxene, phlogopite, perovskite, oxides, apatite, and carbonate, as well as several accessory phases, such as baddeleyite and calzirtite. Their geochemical and petrological features are related to the variable amounts of these minerals. For this part of the project, we have analyzed the concentrations of trace elements in the primary minerals (clinopyroxene, phlogopite, garnet, perovskite, apatite and olivine) identified in three phlogopite-perovskite clinopyroxenites and one perovskite-phlogopite dunite. Analyzing the trace elements in these minerals helped us to better understand the differential settling of minerals within the Salitre magma chamber, and their possible genetic relationship with carbonatitic and lamprophyric rocks. These analyses also provided important information about the minerals' enrichment in rare earth elements (REEs) and high field strength elements (HFSEs). This publication results from work conducted under the transnational access/national open access action at Mass spectrometry la-icp laboratory (IGG-CNR, Italy) supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
The Morro São João intrusion is located in the easternmost part of the Serra do Mar province, along the Cabo Frio lineament (Fig. 1) and has an area of approximately 10 km². It is a Late Cretaceous intrusion formed by clinopyroxenites, melagabbros, shonkinites, malignites, nepheline syenites, and phonolite dikes, without olivine, and is thought to have formed by closed system crystallization of a fairly evolved tephritic melt of potassic/ultrapotassic affinity (cf. Brotzu et al., 2007). We have analyzed two malignites, and specifically, their liquidus phases (clinopyroxene, titanite, garnet, amphibole). Analyzing the trace elements in these minerals helps us to better understand the different fractionation of the elements in these coexisting phases, and the implications for the evolution processes that occurred in the Morro São João magma reservoir. These analyses also provided important information about the concentration of rare earth elements (REEs) and high field strength elements (HFSEs), and their change with the magmatic evolution of the suite. This publication results from work conducted under the transnational access/national open access action at Mass spectrometry la-icp laboratory (IGG-CNR, Italy) supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
This dataset provides rheometric data of the PDMS Korasilon G 20 OH used for analogue modelling at the Laboratory for Experimental Tectonics at GFZ Helmholtz Centre for Geosciences, Potsdam, Germany. The batch number is 1000039264, purchased in 2022 and opened in 2026. The material sample has been analyzed at the Laboratory for Experimental Tectonics at GFZ Helmholtz Centre for Geosciences, Potsdam (HelTec) using an Anton Paar Physica MCR 301 rheometer in a cone-plate configuration at room temperature (21˚C). Rotational (controlled shear rate) tests with shear rates varying from 10^-4 to 10^-1 s^-1 were performed. According to our rheometric analysis, the material is quasi-Newtonian (n~1) at strain rates below 10^-2 s^-1 and weakly shear rate thinning above. The viscosity of G 20 OH is 1.8*10^4 Pa s.
This data set consists of Horizontal-to-Vertical Spectral Ratios (HVSR) resulting from the application of the software package HVNEA (HV Noise and Earthquake Automatic Analysis) with the aim of comparing them with those resulting from the application of another method, namely STATION (Seismic sTATion and sIte amplificatiON). The results, relative to more than 24,000 HVSR, derive from the processing of 700,000 seismograms recorded over different time periods by 8 stations of the networks IV (Italian Seismic Network), GU (Regional Seismic Network of North Western Italy) and GV (Mobile RSNI). To compare the results of the two methods as accurately as possible, the waveforms were subjected to the same preprocessing already used to elaborate the results stored in the STATION database. To this end, the methodological workflow applied with HVNEA for station IV.MURB involved the selection of segments from continuous recordings for each event reported in the INGV catalogue located within a radius of 120 kilometres from the station. Starting from the automatically picked S-wave onsets, 12-second windows were then extracted and used for the analysis of earthquake recordings. Regarding the noise analysis, it should be noted that STATION again considers 12-second windows selected before the P-wave onset, while HVNEA requires the use of a signal window of at least 60 seconds. A window of 3,600 seconds was used for the analysis. The comparison of the HVSR was performed in the frequency band 0.1–15 Hz. All analysed curves, for both earthquake and noise recordings, show generally similar shapes and identify significant peaks in correspondence of the same frequency ranges, although the amplitudes obtained with STATION are systematically higher than those obtained with HVNEA. To obtain a quantitative comparison, various statistical metrics commonly used to measure the discrepancy between data sets were applied, namely the Mean Squared Error, the Mean Absolute Error and the Pearson Correlation Coefficient. This publication results from work conducted under the transnational access/national open access action at the Site effects Laboratory – INGV L’Aquila supported by WP3 ILGE–MEET project, PNRR–EU Next Generation Europe program, MUR grant number D53C22001400005.
The Upper Cretaceous Salitre intrusion, subdivided into Salitre I and Salitre II and dated to ~86-82 Ma by Sonoki and Garda (1988), is part of the Alto Paranaíba Igneous Province (APIP, Fig. 1) in Brazil, which is one of the largest ultrapotassic / carbonatitic / kimberlitic provinces in the world. The intrusion is characterized by the presence of lamproites, carbonatites and one lamprophyre (analyzed here), as well as along with a variety of intrusive cumulitic rocks. Among the Salitre studied samples, this alkaline lamprophyre is characterized by low SiO2 (35.6 wt%), ultrapotassic (K2O/Na2O = 5; K2O = 4.4 wt%) and peralkaline (PI = 1.3). It exhibits variable MgO content (14 wt%) and is enriched in REEs (∑REE=~1,300 ppm) and other trace elements (Nb, Ta, Zr, Hf, Sr, Ba). This lamprophyre is characterized by olivine and phlogopite phenocrysts set in a fine-grained groundmass of clinopyroxene, apatite, phlogopite, magnetite, chromite, and perovskite, with rare titanite and garnet; kalsilite is absent. Analyzing the trace elements of the main minerals in this lamprophyre helped us learn more about the origin and evolution of these magmas, as well as their possible genetic link with the other Salitre rocks. This analysis also provided important information about their enrichment in rare earth elements (REEs) and high field strength elements (HFSEs). This publication results from work conducted under the transnational access/national open access action at Mass spectrometry la-icp laboratory (IGG-CNR, Italy) supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
In this work we aimed to investigate and quantify the relative importance of dynamic conditions (e.g., stirring in a Concentric Cylinder apparatus) on the crystallization kinetics of basaltic magmas (Stromboli). This was achieved by observing the final textures of the samples, analysing the resulting SEM images, and finally relating the resulting parameters to specific growth and nucleation rates. The dataset is made of: 1) A folder called "SEM Images" with two sub-folders inside, representative of the two experiments carried out, called "CG1" and "CG2.3" 2) An Excel file, consisting in 4 data sheets, where all results of image analysis are included, divided in sections. The sheets are also available in CSV format. This publication results from work conducted under the transnational access/national open access action at High Pressure - High Temperature Laboratory (HPHT Lab), Istituto Nazionale di Geofisica e Vulcanologia (INGV), Rome, Italy supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
The Limeira I kimberlite (91±6 Ma; Guarino et al., 2013) is part of the Alto Paranaíba Igneous Province (APIP) and was emplaced in the southern part of the São Francisco Craton in Brazil. This Kimberlite contains macrocrysts and phenocrysts of olivine, resorbed phlogopite/ tetraferriphlogopite, Al-free magnetite, chromite, magnesian ilmenite, rutile, perovskite, monticellite, apatite, serpentine and carbonate. It also contains a suite of xenocrysts and xenoliths (among which we recall wehrlite, phlogopite-ilmenite-websterite, olivine-ilmenite-glimmerite, clinopyroxenites bearing potassic-richterite, chromite-monticellite-kalsilite xenoliths, rutile with priderite or perovskite reaction rims, magnesian chromian ilmenite with perovskite rims). In this part of the project, we analyzed the xenocryst minerals and the main minerals found in the xenoliths entrapped in the Limeira I kimberlite. Analyzing the trace element concentrations in these minerals, helped us to better understand the processes that may occur in the subcontinental lithospheric mantle beneath the Alto Paranaíba Igneous Province. These analyses also provided important information about the minerals' enrichment in rare earth elements (REEs) and high field strength elements (HFSEs). This publication results from work conducted under the transnational access/national open access action at Mass spectrometry la-icp laboratory (IGG-CNR, Italy) supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
The Valles Caldera, New Mexico, USA was created by two caldera-forming eruptions at ~1.6 and ~1.1 Myr. Since then, post-caldera activity has consisted of lava domes, lava flows, large explosive phases, and a hydrothermal system active today. Possibly the youngest eruption sequence, El Cajete, was emplaced 74.4 ± 1.3 ka (Zimmerer et al., 2016) and began with pyroclastic surges, followed by pyroclastic density currents (PDCs) and pumice-rich Plinian pyroclastic fall (Self et al., 1988). The objective of this project was to characterize crystal grains from the early El Cajete sequence, in terms of morphology and textures, using scanning electron microscopy (SEM). The early El Cajete differs from the later part of the sequence in its greater stratigraphic and lithologic complexity, having been formed from not only pyroclastic fall (like the later El Cajete) but also surge beds and PDCs. This dataset was collected under the national open access action at Istituto Nazionale di Geofisica e Vulcanologia, Sezione di Pisa SEM/EDS facility supported by WP3 ILGE – MEET project, PNRR – EU Next Generation Europe program, MUR grant number D53C22001400005. This allowed me to obtain the present dataset of 31 cathodoluminescence (CL) images of 30 quartz crystals and one sanidine crystal.
This data set includes the results of high-resolution digital image correlation (DIC) analysis and digital elevation models (DEM) applied to analogue modelling experiments (Table 1). Six generic analogue models are extended on top of a rubber sheet. In Series A, as extension velocity increases, the initial biaxial plane strain condition evolves into triaxial constrictional or intermediate strain. Models A1 and A2 are two-phase models and Model A3 is a three-phase model. Conversely, in Series B, as extension velocity decreases, the model starts with triaxial constrictional strain and ends up with biaxial plane or intermediate triaxial strain. Models B1and B2 are two-phase models and Model B3 is a three-phase model. Detailed descriptions of the experiments can be found in Liu et al. (2025) to which this data set is supplement. The data presented here are visualized as topography, the horizontal cumulative surface strain, and incremental profiles.
Kamafugites are 'exotic igneous rocks' with mineralogical and chemical compositions that differ from those observed in common magmas. Despite their importance, kamafugites are still a poorly constrained topic and they lack a general petrological model due to their variable petrographic, geochemical and isotopic features. A detailed comparison among kamafugites is necessary to obtain a deeper understanding of the processes involved in their petrogenesis and of their strongly metasomatised mantle sources. Therefore, this data publication doesn’t only provide new geochemical and isotopic data from kamafugites, but a comprehensive data compilation for kamafugite samples in the Western branch of the East Africa Rift (WEAR) in Uganda and Democratic Republic of Congo, the Intra-Apennine Province (IAP), as well as for the Alto Paranaiba (APIP) and Goiás (GAP) provinces in Brazil. 97 kamafugite whole-rock data for the WEAR, 42 for IAP and 51 for APIP and GAP have been collected and compared to highlight similarities and differences, aiming to reconstruct their petrogenesis. The new data in this data publication results from work conducted at Laboratory of Geochronology and Radiogenic Isotope Geochemistry - Pisa1 (IGG-CNR, Italy) supported by WP3 ILGE - MEET project, PNRR - EU Next Generation Europe program, MUR grant number D53C22001400005.
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