Description: This study aimed to constrain the source area of fluids responsible for the formation of a pockmark field in the eastern Red Sea. The newly discovered field extends over an area of at least 1,000 km2 at a water depth of ~400 m. The pockmarks have modal diameters of 140–150 m and are either randomly distributed on the seafloor or aligned within valleys approximately 25 m deep and several kilometres in length. Seismic data show that chimneys and/or regions of acoustic turbidity prevail beneath the pockmark field down to the top of Miocene evaporites, which are widespread in the Red Sea. Four gravity cores were taken from the pockmark field. For most of the cores, geochemical analyses show that porewater has a higher Cl concentration than the local seawater and increased Cl/Br ratios, which indicate an origin from evaporites. The adsorbed hydrocarbons are of thermal origin, with C1/(C2+C3) ratios between 4 and 23 and stable carbon isotope data for methane varying from δ13C of –34 to –36.4‰ with respect to Vienna Pee Dee Belemnite. On the basis of the calculated maturity of the source rock of 1.2–1.4 Ro, local thermal gradients and sedimentation rates, its deeper depth boundary is approximated at 2,000 to 2,200 m. The results indicate that the adsorbed hydrocarbons sampled at the seafloor had to pass through an evaporite sequence of potentially several hundred metres to a few km in thickness. The most likely explanation for the increased permeability of the evaporite sequence is brittle deformation triggered by extensive local tectonic movements and supported by high fluid overpressure within the evaporite sequence.

Description: The major geochemical characteristics of Red Sea brine are summarized for 11 brine-filled deeps located along the central graben axis between 19°N and 27°N. The major element composition of the different brine pools is mainly controlled by variable mixing situations of halite-saturated solution (evaporite dissolution) with Red Sea deep water. The brine chemistry is also influenced by hydrothermal water/rock interaction, whereas magmatic and sedimentary rock reactions can be distinguished by boron, lithium, and magnesium/calcium chemistry. Moreover, hydrocarbon chemistry (concentrations and δ13C data) of brine indicates variable injection of light hydrocarbons from organic source rocks and strong secondary (bacterial or thermogenic) degradation processes. A simple statistical cluster analysis approach was selected to look for similarities in brine chemistry and to classify the various brine pools, as the measured chemical brine compositions show remarkably strong concentration variations for some elements. The cluster analysis indicates two main classes of brine. Type I brine chemistry (Oceanographer and Kebrit Deeps) is controlled by evaporite dissolution and contributions from sediment alteration. The Type II brine (Suakin, Port Sudan, Erba, Albatross, Discovery, Atlantis II, Nereus, Shaban, and Conrad Deeps) is influenced by variable contributions from volcanic/magmatic rock alteration. The chemical brine classification can be correlated with the sedimentary and tectonic setting of the related depressions. Type I brine-filled deeps are located slightly off-axis from the central Red Sea graben. A typical “collapse structure formation” which has been defined for the Kebrit Deep by evaluating seismic and geomorphological data probably corresponds to our Type I brine. Type II brine located in depressions in the northern Red Sea (i.e., Conrad and Shaban Deeps) could be correlated to “volcanic intrusion-/extrusion-related” deep formation. The chemical indications for hydrothermal influence on Conrad and Shaban Deep brine can be related to brines from the multi-deeps region in the central Red Sea, where volcanic/magmatic fluid/rock interaction is most obvious. The strongest hydrothermal influence is observed in Atlantis II brine (central multi-deeps region), which is also the hottest Red Sea brine body in 2011 (~68.2 °C).