ALBERT

Description: Highlights • Sub-basalt imaging improvement on the Vøring Margin • Definition of a new seismic facies unit: the Lower Series Flows • Significant organic carbon content within the melting crustal segment • Apectodinium augustum marker for the PETM is reworked into the Lower Series Flows • The Lower Series Flows, early Eocene in age, predate the Vøring Margin breakup Abstract Improvements in sub-basalt imaging combined with petrological and geochemical observations from the Ocean Drilling Program (ODP) Hole 642E core provide new constraints on the initial breakup processes at the Vøring Margin. New and reprocessed high quality seismic data allow us to identify a new seismic facies unit which we define as the Lower Series Flows. This facies unit is seismically characterized by wavy to continuous subparallel reflections with an internal disrupted and hummocky shape. Drilled lithologies, which we correlate to this facies unit, have been interpreted as subaqueous flows extruding and intruding into wet sediments. Locally, the top boundary of this facies unit is defined as a negative in polarity reflection, and referred as the K-Reflection. This reflection can be correlated with the spatial extent of pyroclastic deposits, emplaced during transitional shallow marine to subaerial volcanic activities during the rift to drift transition. The drilled Lower Series Flows consist of peraluminous, cordierite bearing peperitic basaltic andesitic to dacitic flows interbedded with thick volcano-sedimentary deposits and intruded sills. The peraluminous geochemistry combined with available C (from calcite which fills vesicles and fractures), Sr, Nd, and Pb isotopes data point towards upper crustal rock-mantle magma interactions with a significant contribution of organic carbon rich pelagic sedimentary material during crustal anatexis. From biostratigraphic analyses, Apectodinium augustum was found in the The Lower Series Flows. This species is a marker for the Paleocene – Eocene Thermal Maximum (PETM). However, the absence of very low carbon isotope values (from bulk organic matter), that characterize the PETM, imply that A.augustum was reworked into the early Eocene sediments of this facies unit which predate the breakup time of the Vøring Margin. Finally, a plausible conceptual emplacement model for the Lower Series Flows facies unit is proposed. This model comprises several stages: (1) the emplacement of subaqueous peperitic basaltic andesitic flows intruding and/or extruding wet sediments; (2) a subaerial to shallow marine volcanism and extrusion of dacitic flows; (3) a proto-breakup phase with intense shallow marine to subaerial explosive volcanism responsible for pyroclastic flow deposits which can be correlated with the seismic K-Reflection and (4) the main breakup stage with intense transitional tholeiitic MORB-type volcanism and large subsidence concomitant with the buildup of the Seaward Dipping Reflector wedge.

Description: Organic-rich carbonate sediments are deposited in a range of environments today and in the geologic past. A significant part of organic matter (OM) degradation in such sediments often occurs by microbial reduction of seawater sulfate, and the sulfide product may be preserved in pyrite and in organic sulfur (S) compounds. The isotopic composition (δ34S) of these phases can provide valuable information about S cycling in the ocean and in sediment porewaters, but only insofar as the processes governing these δ34S values are understood. To this end, we investigated the pathways, timing and interactions between pyrite and organic S formation during the deposition of organic-rich chalks. As a test case, we studied cores representing the thickest (∼350 m) and most complete Late Cretaceous organic-rich sequence along the southern Paleotethyan margin (central Israel). The organic S and OM contents show an inverse relation with the pyritic S content, which together with the uniform FePy/FeHR ratio (∼40%), suggest competition between organic S and pyrite formation. Both kerogen and pyritic S are 34S-depleted relative to Late Cretaceous marine sulfate (δ34S∼17–20‰), but the kerogen S is consistently and unusually 34S-enriched relative to coexisting pyrite by up to ∼38‰. Large S isotope fractionation (∼60‰) during microbial sulfate reduction necessary to reproduce the lowest pyrite δ34S values in the core, and relatively invariant δ34S values in organic S suggests that this large fractionation was approximately constant during deposition of the chalks in the core. Higher pyrite δ34S values observed in the most organic-rich parts of the core may be explained by Fe-limited pyrite formation, perhaps due to the reaction of Fe (e.g., complexation, sorption) with organic compounds. Lesser Fe availability, relative to the OM available for sulfate reduction, limits the ultimate abundance of pyrite, but importantly, it delays the formation of pyrite to deeper below the sediment-water interface, from 34S-enriched sulfide produced by Rayleigh distillation of a dwindling sulfate reservoir. Thus, it appears that competing Fe-OM, S-OM and Fe-S reactions can significantly affect the δ34S values recorded in pyrite in organic-rich carbonate sediments despite large and relatively constant microbial S isotope fractionation.

Description: Precipitation chemistry data provide important information for environmental studies on large-scale element cycling and anthropogenic impacts on our atmosphere, but also for hydrochemical models and groundwater recharge estimations via the Chloride Mass Balance method. Such recharge data play a crucial role in groundwater management, particularly in (semi-)arid areas. Unfortunately, precipitation analyses are often scarce in such regions. This also applies to the Arabian Peninsula, including southern Oman. To overcome this lack of rain chemistry data, we developed a strategy for automatic weekly bulk precipitation sampling, using recently designed automatic rainwater samplers. The integral samples were gathered along an elevation gradient from the Salalah coast to the Dhofar mountains during the Indian Ocean Monsoon seasons 2017 and 2018. Our major ion analyses of the rainwater samples revealed considerable temporal and spatial heterogeneity, in terms of ion proportions and absolute concentrations. Samples from the coast were relatively salty (EC mostly 〉3000 μS cm−1) and rich in Na+ and Cl−, reflecting small rain amounts and a sea spray effect. Further inland, solute concentrations were lower, partly due to more precipitation, and ions such as Ca2+ and SO42− gained importance, probably due to calcite and gypsum dust. This pattern reflects the interplay between solute availability (influenced by regional geology, wind direction at different altitudes, and wind speed) and precipitation amounts. Cl−/Br− ratios were fairly uniform and scattered around the seawater value. Combining ion concentrations and rain amounts yielded bulk depositions that showed an erratic pattern along the elevation gradient, i.e., depositions did not decrease steadily in inland direction, as one may assume. This suggests that the occasionally reported approach of collecting a few opportunistic grab samples at a single site is unlikely to yield data that are representative for a larger coastal study area.