The effect of the Fernando de Noronha plume on the mantle lithosphere in north-eastern Brazil

New xenolith occurrences in the Cenozoic alkali basalts of north-eastern Brazil have been studied in order to constrain the possible imprint on the continental mantle lithosphere of its passage over the Fernando de Noronha plume and the regional mantle processes. Texturally, the lherzolite and harzburgite xenoliths define three groups: group 1, porphyroclastic; group 2, protogranular; group 3, transitional between groups 1 and 2. Equilibrium temperatures are highest for group 1 and lowest for group 2. Clinopyroxenes from group 1 peridotites have Primitive Mantle (PM)-normalised REE patterns varying from L-MREE-enriched convex-upward, typical of phases in equilibrium with alkaline melts, to LREE-enriched, spoon-shaped, to LREE-enriched, steadily fractionated in a wehrlite. Group 2 clinopyroxenes show patterns slightly depleted in LREE to nearly flat. The M-HREE are at 3–5 ×PM concentration level, as typical in fertile lithospheric lherzolites. Most of group 3 clinopyroxenes show LREE-depleted patterns similar to the group 2 ones, but in two samples the clinopyroxenes are characterised by LREE-enriched, spoon-shaped profiles. Sr and Nd isotopes of the group 1 clinopyroxenes form an array between DM and EMI-like components, both of them are also present in the host basalts. Melts estimated to be in equilibrium with the group 1 clinopyroxenes having L-MREE-enriched, convex-upward patterns are similar to the Cenozoic alkaline magmas. The groups 2 and 3 clinopyroxenes define two distinct compositional fields at higher ¹⁴³Nd/¹⁴⁴Nd values, correlated with their LREE composition. The isotopes of the groups 2 and 3 LREE-depleted clinopyroxenes form an array from DM towards the isotopic composition of Mesozoic tholeiitic basalts from north-eastern Brazil. Melts in equilibrium with these clinopyroxenes are similar to these basalts, thus suggesting that such xenoliths record geochemical imprint from older melt-related processes.

The LREE-enriched spoon-shaped group 3 clinopyroxenes are characterised by the highest ¹⁴³Nd/¹⁴⁴Nd values at any given ⁸⁷Sr/⁸⁶Sr composition. These results are interpreted in terms of a lithospheric mantle section which underwent thermo-chemical and mechanical erosion by infiltration of asthenospheric alkali basalts having EMI-like isotope characteristics during Cenozoic time. At that time, the lithospheric mantle consisted of fertile lherzolites and harzburgites recording the geochemical imprint of Mesozoic mantle processes. The onset of the interaction between lithospheric peridotites and alkaline melts was characterised by the porous flow percolation of small melt volumes that induced chromatographic enrichments in highly incompatible elements and the isotope signature of the spoon-shaped, group 3 clinopyroxenes. Group 1 peridotites represent the base of the lithospheric column eroded by the ascending alkaline melts, whereas the group 2 documents the shallower lithospheric section, with group 3 being the transition. The similarity of processes and isotope components in the protogranular xenoliths from Fernando de Noronha area and north-eastern Brazil supports the hypothesis that the lithosphere beneath Fernando de Noronha is a detached portion of the continental one. Furthermore, the similarity in terms of textural and geochemical features documented by the mantle samples coming from the two different regions seems to confirm the interference of the two regions with the same plume.     

Application of Binary Permeability Fields for the Study of $${\hbox {CO}_{2}}$$ Leakage from Geological Carbon Storage in Saline Aquifers of the Michigan Basin

The feasibility of geological carbon storage (GCS) sites depends on their capacity to retain safely \({\hbox {CO}_{2}}\). While deep saline formations and depleted gas/oil reservoirs are good candidates to sequester \({\hbox {CO}_{2}}\), gas/oil reservoirs typically have a limited storage capacity compared to ideal targets (\(\sim \) 1 Mt/year) considered for \({\hbox {CO}_{2}}\) disposal (Celia et al. in Water Resour Res 51(9):6846–6892, 2015. doi: 10.1002/2015WR017609). In this respect, deep saline aquifers are considered more appropriate formations for GCS, but present the disadvantage of having limited characterization data. In particular, information about the continuity of the overlying sealing formations (caprock) is often sparse if it exists at all. In this work, a study of \({\hbox {CO}_{2}}\) leakage is conducted for a candidate GCS site located in the Michigan Basin, whose sealing properties of the caprock are practically unknown. Quantification of uncertainty on \({\hbox {CO}_{2}}\) leakage from the storage formation is achieved through a Monte Carlo simulation approach, relying on the use of a computationally efficient semi-analytical leakage model based upon the solution derived by Nordbotten et al. (Environ Sci Technol 43(3):743–749, 2009), which assumes leakage occurs across “passive” wells intersecting caprock layers. A categorical indicator Kriging simulator is developed and implemented to represent the caprock sealing properties and model the permeability uncertainty. Binary fields of caprock permeability are generated and exhibit mostly low permeability, with sparsely-occurring local high permeability areas where brine and \({\hbox {CO}_{2}}\) may leak out of the storage formation. In addition, the feasibility of extending the use of the semi-analytical model to large-area leakage pathways is studied. This work advances a methodology for preliminary uncertainty quantification of \({\hbox {CO}_{2}}\) leakage at sites of GCS with little or no information on the sealing properties of the caprock. The implemented analysis shows that, for the considered site, \({\hbox {CO}_{2}}\) leakage may not be negligible even for relatively low (\(\sim \) 1%) probabilities of finding permeable inclusions in the caprock and highlights the importance of being able to characterize caprock sealing properties over large areas.