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Las algas rojas coralinas (rodofitas) habitan las costas, coloreando estas regiones con una hermosa tonalidad roja o rosada, y son tan duras y afiladas que, de ser pisadas, causarían dolor al pie descalzo. Entre sus diminutas ramas, muchos organismos se desarrollan y encuentran refugio. La fotosíntesis de las algas coralinas conduce a la formación de estructuras de carbonatos con una arquitectura fascinante. Pero tanto el alga como sus microorganismos asociados (microbiota) participan en la formación de estos biominerales, que se acumulan y cementan los materiales que forman las playas y las costas. Los carbonatos son susceptibles a la química ácido-base, por lo tanto, su estabilidad estructural y su disolución dependen del pH del medio que los rodea. Por tanto, estos biominerales y los organismos marinos que los forman (como algas, corales, moluscos o equinodermos) son vulnerables a la acidificación del océano. La curiosidad por ver lo que nuestros ojos no pueden nos llevó a entender que las delicadas ramitas de las algas coralinas esconden una asombrosa fortaleza estructural donde la microestructura y la química son elementos clave, pues encontramos que minerales con una gran estabilidad estructural y térmica constituyen el cuerpo, o talo, de las algas. Hoy en día las algas rojas y verdes coralinas son modelos vivos de gran interés para la ciencia básica, para capturar carbono en estructuras estables. Así, esta área de investigación puede inspirar el desarrollo de estrategias para mitigar el cambio climático.

Coralline algae are worldwide carbonate builders, considered to be foundational species and biodiversity hotspots. Coralline habitats face increasing pressure from human activities and effects related to Global Change, yet their ecological properties and adaptive responses remain poorly understood. The relationships of the algal microbiota with the mineral bioconstructions, as well as plasticity and resilience of coralline holobionts in a changing environment, are of particular interest. In the Gulf of California, Neogoniolithon trichotomum (Rhodophyta) is the main carbonate builder in tidal pools. We performed a multi-disciplinary assessment of the N. trichotomum microstructure using XRD, SEM microscopy and SR-FTIR spectromicroscopy. In the algal perithallus, magnesium-calcite and aragonite were spatially segregated and embedded in a polysaccharide matrix (rich in sulfated polysaccharides). Mg-calcites (18-19 mol% Mg) were the main mineral components of the thallus overall, followed by iron carbonates related to dolomite (ankerite) and siderite. Minerals of late evaporitic sequences (sylvite and bischofite) were also present, suggesting potential halophilic microenvironments within the algal thalli. The diverse set of abundant halophilic, halotolerant and oligotrophic taxa, whose abundance increase in the summer, further suggests this condition. We created an integrated model, based on environmental parameters and the microbiota distribution, that identified temperature and nutrient availability (particularly nitrate and silicate) as the main parameters related to specific taxa patterns. Among these, Hahella, Granulossicoccus, Ferrimonas, Spongiibacteraceae and cyanobacterial Xenococcaceae and Nostocaceae change significantly between seasons. These bacterial components might play relevant roles in algal plasticity and adaptive responses to a changing environment. This study contributes to the understanding of the interplay of the prokaryotic microbiota with the mineral microenvironments of coralline algae. Because of their carbonates with potential resistance to dissolution in a higher pCO2 world and their seasonally dynamic bacteria, coralline algae are relevant targets to study coastal resilience and carbonated systems responses to changing environments.

Microbialites are modern analogs of ancient microbial consortia that date as far back as the Archaean Eon. Microbialites have contributed to the geochemical history of our planet through their diverse metabolic capacities that mediate mineral precipitation. These mineral-forming microbial assemblages accumulate major ions, trace elements and biomass from their ambient aquatic environments; their role in the resulting chemical structure of these lithifications needs clarification. We studied the biogeochemistry and microbial structure of microbialites collected from diverse locations in Mexico and in a previously undescribed microbialite in Cuba. We examined their structure, chemistry and mineralogy at different scales using an array of nested methods including 16S rRNA gene high-throughput sequencing, elemental analysis, X-Ray fluorescence (XRF), X-Ray diffraction (XRD), Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), Fourier Transformed Infrared (FTIR) spectroscopy and Synchrotron Radiation-based Fourier Transformed Infrared (SR-FTIR) spectromicroscopy. The resulting data revealed high biological and chemical diversity among microbialites and specific microbe to chemical correlations. Regardless of the sampling site, Proteobacteria had the most significant correlations with biogeochemical parameters such as organic carbon (Corg), nitrogen and Corg:Ca ratio. Biogeochemically relevant bacterial groups (dominant phototrophs and heterotrophs) showed significant correlations with major ion composition, mineral type and transition element content, such as cadmium, cobalt, chromium, copper and nickel. Microbial-chemical relationships were discussed in reference to microbialite formation, microbial metabolic capacities and the role of transition elements as enzyme cofactors. This paper provides an analytical baseline to drive our understanding of the links between microbial diversity with the chemistry of their lithified precipitations.

In the work, the processes of phase reconstruction and properties of ceramics obtained from high-siliceous clay-sand, clay-cullet, and clay-sand-cullet mixtures are considered. It is possible to perform plastic molding of blanks from the given mixtures due to the presence of montmorillonite in clay and sand and sintering at 800 oC for 8 h under conditions of oxygen deficiency. Depending on the composition of the initial mixtures, specimens ranging in color from gray to black can be obtained. It has been established by the XRD, IR spectroscopy, and electron microscopy methods that the synthesized material is glass ceramics consisting of quartz, feldspars, and a glass phase. Depending on the content of the initial components in the mixtures, it is possible to obtain glass ceramics with high strength properties or coarse-pored glass ceramics whose properties are similar to those of foamed ceramics.

Agricultural soil erosion, both mechanical and eolic, may impact cloud processes as some aerosol particles are able to facilitate ice crystals formation. Given the large agricultural sector in Mexico, this study investigates the ice nucleating abilities of agricultural dust collected at different sites and generated in the laboratory. The immersion freezing mechanism of ice nucleation was simulated in the laboratory via the Universidad Nacional Autónoma de México (UNAM)-Micro Orifice Uniform Deposit Impactor (MOUDI)-Droplet freezing technique (DFT) (UNAM-MOUDI-DFT). The results show that agricultural dust from the Mexican territory promote ice formation in a temperature range from -11.8°C to -34.5°C, with ice nucleating particle (INP) concentrations between 0.11 L-1 and 41.8 L-1. Furthermore, aerosol samples generated in the laboratory are more efficient than those collected in the field, with T50 values (i.e., the temperature at which 50% of the droplets freeze) higher by more than 2.9°C. The mineralogical analysis indicated a high concentration of feldspars i.e., K-feldspar and plagioclase (> 40%) in most of the aerosol and soil samples, with K-feldspar significantly correlated with the T50 of particles with sizes between 1.8 µm and 3.2 µm. Similarly, the organic carbon (OC) was correlated with the efficiency of aerosol samples from 3.2 µm to 5.6 µm and 1.0 µm to 1.8 µm. Finally, a decrease in the efficiency as INPs, after heating the samples at 300°C for 2 h, evidenced that the organic matter from agricultural soils can influence the role of INPs in mixed-phase clouds. [ABSTRACT FROM AUTHOR]

Grain size, heavy minerals, mineralogical, and geochemical analyses were undertaken on the sand samples from Huatabampo (HB) and Altata (AA) beaches to infer palaeoweathering conditions and source rock characteristics. The mean grain size of HB and AA sands is fine‐grained and fine‐ to medium‐grained, respectively. Magnetite and hypersthene are the common heavy minerals identified in HB sands, whereas magnetite and ilmenite are the dominant heavy minerals in AA sands. HB sands have a high proportion of quartz and plagioclase followed by K‐feldspar and zeolite. Quartz is the dominant mineral in the AA sands, followed by plagioclase and K‐feldspar. Geochemically, the sand samples from HB are classified as wacke, whereas AA sands are classified as wacke and arkose. In chondrite‐normalised REE plot, HB and AA sands show LREE enriched and HREE depleted pattern with negative Eu anomaly. Chemical index of alteration (CIA), plagioclase index of alteration (PIA) values and Th/U ratios of HB and AA sands suggest a low intensity of chemical weathering in the source area. The tectonic discriminant function diagram suggestsan arc setting for HB sands, whereas a rift setting for AA sands. The chondrite‐normalised REE patterns, Eu anomaly, Al2O3/TiO2 ratio, trace elemental ratios, discriminant function, and ternary diagrams suggest that the HB and AA sands were dominantly derived from felsic source rocks. The comparison of REE patterns of HB and AA sands with the source rocks exposed near to the study area suggest that the central granites of Laramide plutonic rocks exposed in Sonora were contributing sediments to the HB beach, whereas AA sands received sediments mainly from the felsic Francisco gneiss in the western Sonobari Complex of Sinaloa. [ABSTRACT FROM AUTHOR]

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Fragipan is a compacted but non-cemented subsurface horizon, considered as a pedogenic horizon, but the mechanism of its formation is not well understood. The main hydro-consolidation hypothesis involves a collapse of soil structure when it is loaded and wet, resulting a reorganisation of pore space. Soils with fragipan never have been marked in Russian soil maps. In the South Karelia, located in Eastern Fennoscandia (34.50921 E and 61.33186 N, 110 m asl) we studied a soil profile of Albic Fragic Retisol (Cutanic), developed in the glacial till of Last Glaciation with flat subhorizontal topography under an aspen-spruce forest. The aim of this study was to demonstrate how the fragic horizon was formed in the Retisol located in South Karelia. Observations were made in each soil horizon using micromorphological method, particle size analysis and the study of mineralogical composition of clay fraction by X-ray diffraction. The analysis of the morphological description combined with the laboratory data have led us to the conclusion that the consolidation of the fragipan occurred after the textural differentiation of the profile, following the Atlantic Optimum, and does not depend on the presence of swelling clay minerals. The well-developed argic horizon was probably formed around 6000 years ago, under climatic conditions more favourable for clay illuviation than in present time. Fragipan is supposed to be developed during the Sub-Boreal cooling. [ABSTRACT FROM AUTHOR]