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.
We analyzed concentrations of dissolved and particulate trace metals, including iron (Fe), manganese (Mn), vanadium (V), molybdenum (Mo), thallium (Tl), and rare earth elements (REE), during a mesocosm-based phytoplankton summer bloom mimicking the intertidal zone of the southern North Sea (Jade Bay). The studies aimed to identify key drivers controlling their biogeochemical cycling in dynamic, high-productivity coastal environments. Our results highlight the tidally influenced coastal zone as a critical interface that alters the behavior of supposedly conservative elements such as Mo and Tl (Mori et al., 2021) as well as natural and anthropogenic REE (incl., lanthanum, samarium, and gadolinium) (Mori et al., under review). Trace metal concentrations and shale-normalized REE patterns, determined by quadrupole inductively coupled plasma–mass spectrometry (ICP-MS) and inductively coupled plasma–optical emission spectrometry (ICP-OES), were combined with biogeochemical bulk parameters and pigment-based assessments of phytoplankton growth and community composition (Mustaffa et al., 2020). Trace metal and REE cycling were evaluated in relation to phytoplankton dynamics, particulate organic matter composition (C, N, P), dissolved organic carbon, total dissolved nitrogen, and macronutrient concentrations (nitrate, ammonium, silicate, and inorganic phosphate). The dataset was obtained during a Planktotron-based mesocosm experiment conducted within the framework of the Coastal Ocean Darkening project (Mustaffa et al., 2020).
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.
Recycling von elektronischen Kleingeräten zur Gewinnung von seltenen Erden und Lithium, Maßnahmen zur Verstärkung des Recycling; Berichterstattung der Landesregierung im Ausschuss für Umwelt und Forsten