The Mallorca coastal caves present large amounts of speleothems that have been studied for decades. However, the sedimentary deposits also present in these cases have not been given the same attention. This work is the first study entirely focused on these deposits, specifically the ones found in the Ases cave. These deposits are formed by clay minerals (illitic phases, kaolinite, smectite, and chlorite), calcite and quartz, and minor proportions of dolomite, albite, orthoclase, hematite, and goethite. The grain size and the electron microscopy studies suggested the presence of different sedimentation processes (bedrock degradation, creep or saltation, and suspension) and different origins (authigenic and detrital origins) for the different sediments. Based on these differences, two types of deposits were characterized: autochthonous and allochthonous deposits. The first ones are located on the floor of chambers and corridors in subaqueous zones, indicating the stability of the mixing zone (and therefore the sea level) over time. The second ones appear filling voids on the walls and the ceiling in the terrestrial zone, evidencing the filling of the cavity in the presence of water (during a wet period). These results are very important to complete the understanding of the caves and their evolution and support the relevance of these materials in paleoenvironmental studies.
In order to manage problems arising from rainwater/rock interaction in Miocene sandstones (calcareous litharenites) widely used in various monuments of the Ebro Valley (NE of Spain), a survey has been conducted with particular application to the building and architectural decorative materials of the Cathedral of Huesca. Once the current state of decay was diagnosed and the processes of alteration (enhanced by certain intrinsic factors and their particular exposure to the environmental conditions) were detected, a pre-restoration experimental assay was conducted. On the one hand, to propose the best stone replacement, this study evaluates the compatibility of the available sandstones in the local market based on their intrinsic features, especially those related to hydric behaviour. Once the most suitable sandstone was selected, pore size distributions were determined along with accelerated ageing cycles to show the importance of selecting properly the potential replacement sandstone. In a second step, to determine the effectiveness and long-term efficacy of four water-repellent products, several on-site and laboratory tests were performed. From the experimental results obtained, remedial works have been proposed which will be useful not only for the restoration programme of this monument, but also for other emblematic architectural Heritage in the Ebro Valley.
The utility of the Mg/Ca elemental ratio of calcite ((Mg/Ca)calcite) as a temperature indicator in continental carbonate deposits is a matter of debate due to the different results obtained by diverse authors. In this study, we aimed to test the reliability of the (Mg/Ca)calcite in fluvial carbonates. We selected the recent tufa stromatolite records of four rivers on the Iberian Peninsula for the trace element analysis based on six-monthly sampling. Previous sedimentary and hydrological studies on these fluvial basins provided the information for this work. The water temperature estimates for the stromatolite (Mg/Ca)calcite substantially differed from the measured water temperatures in most of the studied cases. We thus assessed other factors that participate in the control of the Mg partitioning between water and calcite. The correction of the detrital Mg content yielded water temperatures that matched the measured ones in one of the rivers. The (Mg/Ca)water, water discharge and calcite precipitation rates may also occasionally influence the (Mg/Ca)calcite. The six-month behaviour of some of these parameters could interfere with the relationship between the (Mg/Ca)calcite and water temperature. According to these results, and their comparison with other non-marine carbonates, the wide variety of parameters that are involved in the (Mg/Ca)calcite limit it as a geochemical thermometer in continental sedimentary environments.