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Since the industrial revolution, anthropogenic CO2 emissions have caused ocean acidification, which particularly affects calcified organisms. Given the fan-like calcified fronds of the brown alga Padina pavonica, we evaluated the acute (short-term) effects of a sudden pH drop due to a submarine volcanic eruption (October 2011–early March 2012) affecting offshore waters around El Hierro Island (Canary Islands, Spain). We further studied the chronic (long-term) effects of the continuous decrease in pH in the last decades around the Canarian waters. In both the observational and retrospective studies (using herbarium collections of P. pavonica thalli from the overall Canarian Archipelago), the percent of surface calcium carbonate coverage of P. pavonica thalli were contrasted with oceanographic data collected either in situ (volcanic eruption event) or from the ESTOC marine observatory data series (herbarium study). Results showed that this calcified alga is sensitive to acute and chronic environmental pH changes. In both cases, pH changes predicted surface thallus calcification, including a progressive decalcification over the last three decades. This result concurs with previous studies where calcareous organisms decalcify under more acidic conditions. Hence, Padina pavonica can be implemented as a bio-indicator of ocean acidification (at short and long time scales) for monitoring purposes over wide geographic ranges, as this macroalga is affected and thrives (unlike strict calcifiers) under more acidic conditions.

Calcite is the most stable polymorph of calcium carbonate (CaCO3) under ambient conditions and is ubiquitous in natural systems. It plays a major role in controlling pH in environmental settings. Electrostatic phenomena at the calcite–water interface and the surface reactivity of calcite in general have important environmental implications. They may strongly impact nutrient and contaminant mobility in soils and other subsurface environments, they control oil recovery from limestone reservoirs, and they may impact the safety of nuclear waste disposal sites. Besides the environmental relevance, the topic is significant for industrial applications and cultural heritage preservation. In this study, the structure of the calcite(104)–water interface is investigated on the basis of a new extensive set of crystal truncation rod data. The results agree with recently reported structures and resolve previous ambiguities with respect to the coordination sphere of surface Ca ions. These structural features are introduced into an electrostatic three-plane surface complexation model, describing ion adsorption and charging at the calcite–water interface. Inner surface potential data for calcite, as measured with a calcite single-crystal electrode, are used as constraints for the model in addition to zeta potential data. Ion adsorption parameters are compared with molecular dynamics simulations. All model parameters, including protonation constants, ion-binding parameters, and Helmholtz capacitances, are within physically and chemically plausible ranges. A PhreeqC version of the model is presented, which we hope will foster application of the model in environmental studies.

Environmental contextAntimony is a trace element ubiquitously present in the environment, but data are lacking on its spatio-temporal distribution in aquatic environments. Long-term records serve as essential tools to decipher temporal patterns, historical sources and sinks and background concentrations in an area. We characterise the temporal concentrations, transport and behaviour of antimony in the Garonne River watershed, the main tributary to the Gironde Estuary, the largest estuary in south-west Europe. AbstractKnowledge of the environmental chemistry of antimony (Sb) in aquatic systems is limited, and a better understanding of its geochemical behaviour is needed. Based on a fourteen-year survey (2003–2016) with monthly measurements of dissolved and particulate Sb at five sites in the Lot–Garonne river system, combined with daily measurements of water discharge and suspended particulate matter, this work characterises Sb behaviour in the upstream major river watershed of the Gironde Estuary. The survey provides a first regional geochemical Sb background in the Garonne River watershed for dissolved (~0.2 µg L−1) and Th-normalised particulate Sb (Sbp/Thp ~0.25) concentrations. Observed decreasing temporal trends (<1 ng L−1 in dissolved and <0.02 mg kg−1 in particulate concentrations per month) at sites representing natural concentrations probably reflect global atmospheric Sb dynamics at the watershed scale. Regular seasonal cycles of solid/liquid partitioning, with higher solubility in summer (matching high dissolved and low particulate concentrations), reflect water-discharge and suspended particulate matter transport dynamics and possibly seasonal (bio)geochemical processes. Furthermore, this coefficient decreases from the river to the estuarine reaches (from average log10Kd 4.3 to minimum 3.7 L kg−1), suggesting an increased solubility of Sb in estuarine systems. Flux estimates indicate the relevance of the dissolved fraction in Sb transport (with negligible influence of the colloidal fraction) and a total flux (dissolved + particulate) entering the Gironde Estuary of 5.66 ± 2.96 t year−1 (~50 % particulate). These results highlight the importance of timescales and environmental parameters for understanding and prediction of future Sb biogeochemistry.

The rheological properties of fresh cement paste are highly influenced by a large number of parameters, among which the most important factors are the applied shear stress, and the shear history, the age of the sample and the temperature. The effects of these parameters on the yield stress (designated as structural limit stress in this work), the viscosity and the structural recovery rate (i.e., the change in dynamic viscosity with time at rest) were studied. In parallel, the changes in ion composition of the carrier liquid, mineral phase content and granulometry were investigated. The results reveal that all investigated rheological parameters exhibit an approximated bi-linear trend with respect to the degree of hydration, with a period of quasi-constant properties until a degree of hydration of approximately 0.07, followed by a non-linear increase. This increase could be attributed to the formation of calcium hydroxide (CH) and calcium-silicate-hydrate (C-S-H) via calorimetry results. With regard to the effect of the shear history of the sample on the rheological properties, the structural limit stress showed a minor dependency on the shear history immediately after the end of shearing, which, however, vanished within the first minute at rest. The same is true for the structural recovery rate. The presented results give detailed insights into the influences of hydration and shear on the rheological properties-especially the thixotropy-of fresh cement pastes.

Nouveau modèle analytique pour une meilleure estimation des flux nets annuels en métaux dissous. Cas du cadmium dans l'estuaire de la Gironde New computation for a better estimation of the annual dissolved metal net fluxes. The case of the cadmium in the Gironde estuary Abstract -Despite major management efforts initiated in 1987 and 2007 and decreasing emissions in the Gironde watershed, cadmium (Cd) levels in oysters from the downstream Gironde estuary are still higher to the consumption limit (5 mg/kg, dw, EC). Dissolved Cd concentrations were measured in surface water collected in the Gironde estuary during nine cruises (2014 -2015). The obtained theoretical (Cd d 0 ) concentrations and the daily net Cd d fluxes, using the Boyle's method, confirm a decadal stepping decrease of the Cd pollution corresponding to that observed in the oysters from the long term national monitoring for priority contaminants at the estuary mouth. As this observation invalidates the previous estimating methods for estimating annual net Cd d fluxes, we propose an original empirical model applicable for the four last decades. This model is based on four exponential functions with defined boundaries for low water discharges. Each of them is representative of one distinct situation of Cd pollution in the watershed relative to major remediation processes implemented in the last four decades. These results allow to develop a direct estimation of the annual net Cd d fluxes only based on the data of the annual mean discharge. Thus, this study demonstrates the strength of the field research in geochemistry to obtain a better quantification of the exportation of dissolved bioavailable pollutants from the continental watersheds to the coastal ocean.