We summarise 15 years of field and remote monitoring of Tapado Glacier in north-central Chile (30° S). Observations include meteorological records, direct mass balance measurements, uncrewed aerial vehicle surveys and tri-stereo satellite imagery for deriving high-resolution elevation changes. Frequent droughts and a significant warming trend of 0.29°C decade−1 since 1974 have caused a decrease in glacier surface albedo and an accelerated loss of glacier area and mass, particularly since the onset of the Chilean Megadrought in 2010, associated here with a 43% winter precipitation deficit. Geodetic estimates indicate increasingly more negative mass balance, varying from slightly negative before 2000 to −0.18 ± 0.35 m w.e. a−1 in 2000–12, −0.44 ± 0.11 m w.e. a−1 in 2012–20 and −0.75 ± 0.12 m w.e. a−1 after 2020. Glacier mass loss is associated with several morphological changes, such as increased penitente height, a larger total surface area of ice cliffs and supraglacial ponds over the debris-covered section and more frequent falls of snow and ice from marginal ice surrounding a steep area of exposed bedrock. Tapado Glacier exemplifies how glacier mass loss is driven by various processes, requiring multiple monitoring techniques, and highlights the accelerated changes of the Andes cryosphere.

Since 2002, legislation in Spain has allowed for the creation and documentation of end-of-life decisionmaking. Over the intervening years, the actual implementation of such documents is very low. Through extensive analysis of the literature, this article explores the current status of the use of and attitudes toward advance directives in Spain and then proposes strategies for improvement in their implementation.

The aim of this research was to investigate the influence of substrate roughness on the adhesion and tribological performance of thin TiN coatings obtained by physical vapor deposition. For that purpose, substrates of AISI H13 steel with surface finishes of 0.06, 0.28 and 0.90 μm in Ra were coated with TiN under the same coating conditions. The chemical composition of the steel, as well as that of the TiN coating, were obtained using EDS analysis. Adhesion tests were carried out following the procedure of BSi 1071-8 standard while hardness was evaluated by ASTM C 1327-03. On the other hand, dry sliding friction tests were conducted with a pin-on-disk tribometer, according to the ASTM G 99-05 standard. This study showed that the roughness of the coating increases as the substrate roughness increases. Regarding adhesion and hardness, all the samples showed an adhesion class 1 according to the standard and a hardness value of 14.51 GPa. Nevertheless, the highest substrate roughness produced the best adhesion. On the other hand, the lowest values for the friction coefficient and wear behavior were obtained by the sample with the lowest substrate roughness of 0.06 µm. In addition, it was found that friction and wear increase when the substrate roughness increases.

Sol-gel coatings show an excellent chemical stability, oxidation control and enhanced corrosion resistance for metal substrates. An organic-inorganic hybrid consisting of poly (methyl methacrylate) (PMMA) and silica (SiO2) was successfully synthesized in the form of solution, by using 3-(trimethoxysilyl) propyl methacrylate (TMSPM) as a coupling agent and cohydrolyzed with tetraethyl orthosilicate (TEOS) to afford chemical bondings to the forming silica networks by a sol-gel method. The as-synthesized hybrid material was subsequently characterized by Fourier Transformation infrared (FTIR) spectroscopy. PMMA-SiO2 was applied as a protective film on hardness steel substrates by dip-coating. The thickness of the coating was 25 µm, while the roughness Ra = 0.6 µm. The wear and friction behavior of the coating on hardened steel (HS) was evaluated by a ball-on-disk test in dry conditions with a AISI steel ball as counterface applying 2, 4, 6, 8 and 10 N normal loads. Friction coefficient values (µk) were in the range of 0.76 to 0.99, whereas the lowest wear rate (k) was observed at 6N with a value of 1.30x10-4 (mm3(Nm)-1).

The disulfide bond pattern of catrocollastatin-C was determined by N-terminal sequencing and mass spectrometry. The N-terminal disintegrin-like domain is a compact structure including eight disulfide bonds, seven of them in the same pattern as the disintegrin bitistatin. The protein has two extra cysteine residues (XIII and XVI) that form an additional disulfide bond that is characteristically found in the disintegrin-like domains of cellular metalloproteinases (ADAMs) and PIII snake venom Zn-metalloproteinases (SVMPs). The C-terminal cysteine-rich domain of catrocollastatin-C contains five disulfide bonds between nearest-neighbor cysteines and a long range disulfide bridge between CysV and CysX. These results provide structural evidence for a redefinition of the disintegrin-like and cysteine-rich domain boundaries. An evolutionary pathway for ADAMs, PIII, and PII SVMPs based on disulfide bond engineering is also proposed.