The Abu Ruweis Formation, NW Jordan, was studied with regard to its chemical (major, minor elements, REE, S-, O-, C isotopes, organic chemistry), mineralogical compositions (rock-forming minerals), coal petrography (maceral analyses) and palynology (age determination and palaecosystem) for the evaporite–coal facies transition which is very rarely found. The palynomorphs point to a Late Triassic/Carnian age of formation. Strong evaporation in the series is demonstrated by the presence of dolomite, gypsum and celestite. Mg, Ca, F, Cl, S, Sr and Ba reflect the variation of evaporation during basin subsidence. A detrital influx is characterized by the abundance of Si, Ti, Al, Fe, Mn Ce, Co, Cr, V, Y and the (Zr+Rb)/Sr ratio. Salinity variation may be characterized by the fractionation of LREE (La) and HREE (Lu). The element triplet Zn, Cu and Pb offers a clue to the redox regime and supports the idea of mineralogical-based proximity indicators: Zn (Eh≪0)⇒Cu (Eh≤0)⇒Pb (Eh≤0). Oxygen isotope composition (δ18O −8.3 to −0.9‰) of the carbonate fraction resulted in uniform isotope formation temperatures near 50°C. Temperature data obtained during coal petrography yielded maximum paleotemperatures of 100°C for the black shale and about 70°C for the remaining coal samples that are likely to reflect hot brine activity in some parts of the basin. The carbon isotopic composition (δ13C −12.4 to −3.9‰) of the carbonate fractions indicates a biogenic 12C-enriched CO2 source, which probably was admixed to marine pore water bicarbonate (with δ13C near 0‰) during early diagenesis. The S isotope composition (sulfide fraction −28.9 to −24.0‰) is typical of sulfides formed in the course of bacterial reduction with some sulfate (sulfate fraction +7.5 to +11.6‰) resulted from later re-oxidation of the sulfides. Phosphate distribution is a measure for the aridity while high-sulfur contents in the coal-bearing sediments point to brackish or alkaline waters. The results of the organic chemistry are interpreted in terms of a bloom of algae which were preserved during dysaerobic conditions in the course of early diagenesis. Sesqui- and diterpenoids are most probably derived from precursor molecules abundant in leaf resins of conifers. Phenanthrene and its methylated analogues derived from combustion products of fossil fuels generated by wild fires. Among the maceral types, textinites A and B represent xylem features of tree trunks and the crassi-cutinite upper leaf cuticles. The data allow for a definition of a special geological setting called the “Arabian Keuper Facies”. This facies type is characterized by an evaporite–coal transition which translates into a geodynamic setting positioned between the fully marine “Alpine Triassic Facies” of the Tethyan Ocean where submarine brines were responsible for the Alpine-type MVT Pb–Zn deposits and the epicontinental “Germanic Keuper Facies” that lacks both hydrothermal activity and major marine incursions.
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