ALBERT

Description: The Cretaceous period (~145–65 m.y. ago) was characterized by intervals of enhanced organic carbon burial associated with increased primary production under greenhouse conditions. The global consequences of these perturbations, oceanic anoxic events (OAEs), lasted up to 1 m.y., but short-term nutrient and climatic controls on widespread anoxia are poorly understood. Here, we present a high-resolution reconstruction of oceanic redox and nutrient cycling as recorded in subtropical shelf sediments from Tarfaya, Morocco, spanning the initiation of OAE2. Iron-sulfur systematics and biomarker evidence demonstrate previously undescribed redox cyclicity on orbital time scales, from sulfidic to anoxic ferruginous (Fe-rich) water-column conditions. Bulk geochemical data and sulfur isotope modeling suggest that ferruginous conditions were not a consequence of nutrient or sulfate limitation, despite overall low sulfate concentrations in the proto–North Atlantic. Instead, fluctuations in the weathering influxes of sulfur and reactive iron, linked to a dynamic hydrological cycle, likely drove the redox cyclicity. Despite the potential for elevated phosphorus burial in association with Fe oxides under ferruginous conditions on the Tarfaya shelf, porewater sulfide generation drove extensive phosphorus recycling back to the water column, thus maintaining widespread open-ocean anoxia.

Description: Unconformity-related hydrothermal ore deposits typically form by mixing of hot, deep, rock-buffered basement brines and cooler fluids derived from the surface or overlying sediments. Current models invoking simultaneous downward and upward flow of the mixing fluids are inconsistent with fluid overpressure indicated by fracturing and brecciation, fast fluid flow suggested by thermal disequilibrium, and small-scale fluid composition variations indicated by fluid inclusion analyses. We propose a new model where fluids first descend, then evolve while residing in pores and later ascend. We use the hydrothermal ore deposits of the Schwarzwald district in southwest Germany as an example. Oldest fluids reach the greatest depths, where long residence times and elevated temperatures allow them to equilibrate with their host rock, to reach high salinity, and to scavenge metals. Youngest fluids can only penetrate to shallower depths and can (partially) retain their original signatures. When fluids are released from different levels of the crustal column, these fluids mix during rapid ascent in hydrofractures to form hydrothermal ore deposits. Mixing from below during ascent provides a viable hydromechanical mechanism to explain the common phenomenon of mixed shallow and deep fluids in the formation of hydrothermal ore deposits.

Description: Fluid mixing across unconformities between crystalline basement and overlying sedimentary basins is commonly invoked as an efficient chemical mechanism for ore deposition, but the origin of basement brines and the process of ore formation have rarely been linked by direct evidence. Using laser ablation–inductively coupled plasma–mass spectrometry microanalysis of individual fluid inclusions with an improved detection approach for anion components, we determined simultaneously the ore metal concentrations and the Cl/Br ratio in texturally well constrained inclusion assemblages from a basement-hosted quartz-fluorite-barite-Pb-Zn vein system. An inverse correlation between the Pb + Zn concentrations and the Cl/Br mass ratios in the fluid inclusions provides clear evidence for mixing of a basement-derived metal-rich brine and a metal-poor formation water that acquired its salinity from halite dissolution in Triassic evaporites of the sedimentary cover. This mixing of two distinct brines with comparable salinity is recorded during the growth of individual quartz crystals containing small galena inclusions, demonstrating the transient and episodic nature of fluid mixing during mineral deposition.

Description: Petroleum source rocks are strongly enriched in organic carbon (OC), and their trace metal (TM) contents often reach low-grade ore levels. The mechanisms leading to these coenrichments are important for understanding how extreme environmental conditions support the formation of natural resources. We therefore studied organic-rich Eocene marls and limestones (oil shale) from the central Jordan Amzaq-Hazra subbasin, part of a Cretaceous–Paleogene shelf system along the southern Neo-Tethys margin. Geochemical analyses on two cores show highly dynamic depositional conditions, consistent with sedimentological and micropaleontological observations. Maximum and average contents, respectively, in OC (~26 and ~10 wt%), sulfur (~7 and ~2.4 wt%), phosphorus (~10 and ~2 wt%), molybdenum (〉400 and ~130 ppm), chromium (〉500 and ~350 ppm), vanadium (〉1600 and ~550 ppm) and zinc (〉3800 and ~900 ppm) are exceptional, in particular without any indication of hydrothermal or epigenetic processes. We propose a combination of two processes: physical reworking of OC- and metal-rich material from locally exposed Cretaceous–Paleogene sediments (as supported by reworked nannofossils), and high marine productivity fueled by chemical remobilization of nutrients and metals on land that sustained anoxic-sulfidic conditions. Burial of high-quality organic matter (hydrogen index 600–700 mgHC/gOC) was related to strongly reducing conditions, punctuated by only short-lived oxygenation events, and to excess H 2 S, promoting organic matter sulfurization. These processes likely caused the OC and TM coenrichments in a high-energy shallow-marine setting that contradicts common models for black shale formation, but may explain similar geochemical patterns in other black shales.