Global nature of the Paleoproterozoic Lomagundi carbon isotope excursion: A review of occurrences in Brazil,India, and Uruguay

Positive carbon isotope excursion is reported from Paleoproterozoic carbonates of the Aravalli Supergroup (northwestern India), the Minas Supergroup (Brazil), and new sections of the Paso Severino Formation (Uruguay). The 2.42 Ga Gandarela Formation, Minas Gerais, Brazil, contains red carbonate-facies BIF grading into dolostones and limestones and yielding δ¹³C values ranging from −1.6 to +0.4‰ V-PDB. The positive C-isotope excursion (up to + 11‰ V-PDB) in marine shallow-water carbonates in India and Brazil (Jhamarkotra Formation in northwestern India, and Cercadinho and Fecho do Funil formations in Minas Gerais State, Brazil) is comparable to that observed in 2.22–2.1 Ga carbonate successions worldwide that were deposited during the Lomagundi excursion. In Uruguay, δ¹³C values up to +11.6‰ V-PDB in the deep-water Paso Severino Formation of the Piedra Alta Terrane are compatible with deposition at ca. 2.15 Ga, as indicated by the 2146 ± 7 Ma U–Pb age of dacites occurring at the top of the unit. Negative δ¹³C values are also present in carbonates of the Paso Severino Formation, but an origin related to organic-matter remineralization cannot be ruled out. Thin carbonate beds in the Rio Itapicuru greenstone belt, Bahia State, Brazil, are associated, as in the Paso Severino Formation, with deep-water black shales and have carbon isotope values up to +9‰ V-PDB. High metamorphic grade carbonates of the Jacurici terrane in the Medrado-Ipueira area, Bahia, Brazil, have carbon isotope values up to +6.9‰ V-PDB, consistent with their minimum age of 2085 ± 5 Ma inferred from the intrusive contact with and the age of the Medrado norite. No evidence was found in India, Brazil, or Uruguay for Paleoproterozoic glacial events recognized in the 2.45–2.22 Ga sedimentary successions worldwide. Unconformities between the Gandarela and Cercadinho formations in Brazil and the banded gneissic Complex and the Lower Aravalli Supergroup in India might explain the absence of glacial record. Compositional and isotopic data presented here for studied Paleoproterozoic carbonate successions allow their integration into the global record of the Paleoproterozoic evolution as well as correlation with other successions of similar age. The study highlights the global nature of the Lomagundi excursion. Furthermore, it indicates that the Lomagundi excursion is recorded in both shallow-water (Aravalli and Minas supergroups) and deep-water carbonates (Paso Severino Formation and Rio Itapicuru greenstone belt) negating a significant impact of stromatolite productivity and hypersaline conditions on carbon isotope values of carbonates deposited in shallow-water, open-marine and isolated basins.     

Isotope stratigraphy of Neoproterozoic cap carbonates in the Araras Group, Brazil

The Neoproterozoic carbonate sequence on the southeastern border of the Amazon Craton is divided into three lithostratigraphic units: a basal cap dolomite, an intermediate limestone, limestone-mudstone unit, and an upper dolarenite-dolorudite unit. Sections of the cap-carbonate were measured from the inner shelf to the outer shelf. Carbon isotope ratios (relative to PDB) vary between − 10.5 and − 1.7‰ in cap dolomite, and between − 5.4 and + 0.1‰ in laminated limestone and mud-limestone. Limestones and mud-limestones exhibit ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.70740 to 0.70780. A comparative isotope stratigraphy between the inner-shelf and the middle-shelf basin shows differences in carbon isotope ratios: The cap dolomite and limestones have lower δ¹³C ratios on the border of the basin (inner shelf) than in the middle shelf of the basin. These lower values can be related to shallower environmental conditions and to a stronger influence of the continental border. The ⁸⁷Sr/⁸⁶Sr ratios are the same in both areas, and are consistent with seawater composition at around 600 Ma.     

The Mantos Blancos copper deposit: an upper Jurassic breccia-style hydrothermal system in the Coastal Range of Northern Chile

The Upper Jurassic Mantos Blancos copper deposit (500 Mt at 1.0% Cu), located in the Coastal Range of northern Chile, displays two superimposed hydrothermal events. An older phyllic alteration probably related to felsic magmatic–hydrothermal brecciation at ∼155 Ma, and younger (141–142 Ma) potassic, propylitic, and sodic alterations, coeval with dioritic and granodioritic stocks and sills, and dioritic dikes. Main ore formation is genetically related to the second hydrothermal event, and consists of hydrothermal breccias, disseminations and stockwork-style mineralization, associated with sodic alteration. Hypogene sulfide assemblages show distinctive vertical and lateral zoning, centered on magmatic and hydrothermal breccia bodies, which constitute the feeders to mineralization. A barren pyrite root zone is overlain by pyrite-chalcopyrite, and followed upwards and laterally by chalcopyrite-digenite or chalcopyrite-bornite. The assemblage digenite–supergene chalcocite characterizes the central portions of high-grade mineralization in the breccia bodies. Fluid inclusions show evidence of boiling during the potassic and sodic alteration events, which occurred at temperatures around 450–460°C and 350–410°C, and salinities between 3–53 and 13–45 wt% NaCl eq., respectively. The hydrothermal events occurred during episodic decompression due to fluid overpressuring, hydrofracturing, and sharp changes from lithostatic to hydrostatic conditions. Sulfur isotope results of hypogene sulfide minerals fall in a narrow range around 0 per mil, suggesting a dominance of magmatic sulfur. Carbon and oxygen isotopic data of calcites from propylitic alteration suggest a mantle-derived carbon and oxygen isotope fractionation due to low-temperature alteration.     

Large-scale silicate liquid immiscibility: a possible example from northeastern Brazil

Ultrapotassic, peralkalic silica-saturated plutons (580 Ma) are widespread in the Cachoeirinha-Salgueiro foldbelt, northeastern Brazil. They consist of alkali-feldspar syenites with pyroxenite as co-magmatic inclusions and syn-plutonic or late-stage dikes. Pyroxenite and syenite have the same mineral phases (aegirine-augite, microcline, sphene, apatite, blue amphibole, magnetite), but only in different proportions. Rare inclusions of a “mixed” rock (about 60% syenite+40% pyroxenite in an emulsion-like texture) are also present. Pyroxenes in the three units are all only slightly zoned, silica-saturated and extremely low in Al₂O₃ (0.2–1.4%). Amphiboles are mostly K-rich richterite, characterized by high SiO₂, low Al₂O₃ and TiO₂ contents and low Mg#.

The three rock types have similar REE chondrite-normalized patterns, with negative slopes and lack of Eu anomaly, with the total REE in the pyroxenite greater than that of the syenite. Trace element patterns for the mixed rock are intermediate between those for the pyroxenite and syenite. Major element partitioning between pyroxenite and syenite has the same sense as that one observed between immiscible liquids in volcanic lavas and trace element partitioning is similar to the experimentally determined partition of immiscible liquid pairs.

The rocks have similar high δ¹⁸O values (avg. w.r.+ 8‰_SMOW, corrected from pyroxene), high initial ⁸⁷Sr/⁸⁶Sr ratios (about 0.710), and low ¹⁴³Nd/¹⁴⁴Nd (avg. 0.51104).

Field and geochemical characteristics indicate chemical equilibrium among the three rock types and suggest liquid immiscibility between syenite and pyroxenite, the mixed rock representing the original magma composition.     

Petrography and stable isotope geochemistry of the cretaceous El Abra Limestones (Actopan), Mexico: Implication on diagenesis

Petrography and stable isotopes (carbon and oxygen) geochemistry of limestones from the El Abra Formation, Actopan, were studied to identify their digenetic environments. The major petrographic types identified are mudstone, wackestone, grainstone, and boundstone. Most of the studied samples show positive δ¹³C values, except two samples (2 and 28), which are slightly negative values (−0.27‰ and −0.02‰). The organic remains identified in foraminiferal wackestone type can be responsible for the negative δ¹³C values. The δ¹⁸O values range from −12.41‰ to −4.02‰ and indicate meteoric diagenesis.