Permanent Scatterers for landslide investigations: outcomes from the ESA-SLAM project

Within the SLAM project (Service for Landslide Monitoring), launched in 2003 by the European Space Agency (ESA) the Permanent Scatterers (PS) technique, a multi-image interferometric approach, coupled with the interpretation of aerial-photos and optical satellite images, was carried out for landslide investigations. The PS analysis was applied at a regional scale as support for landslide inventory mapping and at local scale for the monitoring of single well-known slope movements. For the integration of the PS measurements within a landslide inventory the Arno river basin (Italy) was chosen as test site for the presence of a high number of mass movements (to date about 300 areas at high landslide risk and more than 27,000 individual landslides mapped by the institutional authorities). About 350 SAR images have been interferometrically processed by means of the PS technique, with the detection of about 600,000 PS. The use of optical images contributed spatial meaning to the point-wise information provided by the PS, making it easier to identify terrain features related to slope instability and the landslide boundaries. Here we describe the employed methodology and its impact in the updating of a preexisting landslide inventory. 6.8% of the total number of landslides were characterized by ground displacement measurements from the PS: 6.1% of already mapped landslides and 0.8% of new unstable areas detected through the PS analysis. Moreover, most of the PS are located in urban areas, showing that the proposed methodology is suitable for landslide mapping in areas with a quite high density of urbanization, but that over vegetated areas it still suffers from the limitations induced by the current space-borne SAR missions (e.g. temporal de-correlation). On the other hand, the use of InSAR for the monitoring of single slow landslides threatening built-up areas has provided satisfactory results, allowing the measurement of superficial deformations with high accuracy on the landslide sectors characterized by a good radar reflectivity and coherence.     

Mid-Holocene emergence of southern Tunisian coasts

We present new sea-level data from the coasts of southern Tunisia, between the Gulf of Gabès and the Libyan border. The work tests, previously, published evidence on Holocene shorelines, and confirmed that a distinct emergence has occurred in this area during this time. The emergence peak lies at least 186 ± 11 cm above present and is inferred from: (1) AMS radiocarbon dates of subtidal vermetids and boring shells collected in growth position, and (2) careful assessment of tidal heights. Maximum emergence took place between about 6000 and 5000 ¹⁴C years BP; it cannot be ascribed to tectonics and is probably related to post-glacial hydro-isostatic effects. It challenges the inference of a 3-m global sea-level rise since 6000 years BP due to residual Antarctic melting.     

A clinopyroxene geobarometer for basaltic systems based on crystal-structure modeling

 The crystal chemical response of basalt clinopyroxene to increasing pressure was investigated by means of crystal-structure simulation (a procedure that enables modeling of the structural parameters of a clinopyroxene of known chemistry without requiring direct X-ray diffraction analysis) using available experimental chemical data. Pressure proved the main physical variable governing clinopyroxene behavior in a magmatic environment. The general internal consistency of the simulation data permitted construction of an empirical geobarometer based on the relationship of cell volume (Vc) vs M1-site volume (VM1). The straightforward geobarometric formulation in the absence of direct X-ray analysis is: P(kbar)=698.443+4.985⋅Al_T−26.826⋅Fe²⁺ _M1−3.764⋅Fe³⁺ +53.989⋅Al_M1+3.948⋅Ti+14.651⋅Cr −700.431⋅Ca−666.629⋅Na−682.848⋅Mg_M2−691.138⋅Fe²⁺ _M2−688.384⋅Mn−6.267⋅(Mg_M2)²−4.144⋅(Fe²⁺ _M2 where: (Fe²⁺ _M1⋅Mg_M2)/(Fe²⁺ _M2⋅Mg_M1)=e^**(0.238⋅R³⁺+0.289⋅CNM−2.315), CNM=Ca+Na+Mn, and R³⁺=Al_M1+Fe³⁺+Ti+Cr, with cations in atoms per formula unit. The geobarometer reproduces experimental pressures within ±2 kbar (=1σ; max. dev. ≤5 kbar; N=29) in the range 0–24 kbar and is applicable to near-liquidus C2/c clinopyroxenes crystallized from basaltic melts in the absence of garnet (excepting high-Al₂O₃ basalts). It is therefore suitable for many natural clinopyroxenes occurring as mega- or phenocrysts or forming well-preserved cumulate pyroxenites. If the above restrictions are not wholly satisfied, the Vc vs VM1 plot can also be used qualitatively to deduce the relative pressure conditions of clinopyroxenes forming from similar batches of magma. The structural simulation of experimental data also provided insight into the influence of minor chemical changes of the parental magma on the crystal chemistry of clinopyroxene at high pressure. Within the considered compositional space at given P-T, a _CaO and a _SiO2 in the melt have opposite effects on M2- and T-site cation populations. As a result, under similar physical conditions, clinopyroxenes from higher-CaO or more undersaturated basalts have higher VM2, VT and Vc and lower VM1. For basalts with normal contents of Al₂O₃ (<18 wt %), variations of major elements in the melt do not reduce the accuracy of the geobarometer. Received: 3 April 1994 / Accepted: 23 December 1995     

Certain particular solutions of the clairaut equation

A study has been conducted to ascertain conditions on the density distribution within a fluid, rotating planet in order that the deformation of its outer shell be expressible in terms of the Bessel functions of the first kind and the Gaussian hypergeometric series.It has been established that (1) the density must be a solution to an ordinary differential equation of the Riccati type, and (2) two already considered density distributions are the only closed-form solutions of physical relevance.     

Modelling of mantle postglacial relaxation in axisymmetric geometry with a composite rheology and a glacial load interpolated by adjusted spherical harmonics analysis

Although studies on glacial isostatic adjustment usually assume a purely linear rheology, we have previously shown that mantle relaxation after the melting of Laurentide ice sheet is better described by a composite rheology including a non-linear term. This modelling is, however, based on axially symmetric geometry and glacial forcing derived from ICE-3G and suffers from a certain amount of arbitrariness in the definition of the ice load. In this work we apply adjusted spherical harmonics analysis to interpolate the ice thicknesses of ICE-3G and ICE-1 glaciological models. This filters out the non-axisymmetric components of the ice load by considering only the zonal terms in the spherical harmonics expansion. The resulting load function is used in finite-element simulation of postglacial rebound to compare composite versus purely linear rheology. Our results confirm that composite rheology can explain relative sea level (RSL) data in North America significantly better than a purely linear rheology. The performance of composite rheology suggests that in future investigations, it may be better to use this more physically realistic creep law for modelling mantle deformation induced by glacial forcing.     

Experimental calibration of vanadium partitioning and stable isotope fractionation between hydrous granitic melt and magnetite at 800 °C and 0.5 GPa

Vanadium has multiple oxidation states in silicate melts and minerals, a property that also promotes fractionation of its isotopes. As a result, vanadium isotopes vary during magmatic differentiation, and can be powerful indicators of redox processes at high temperatures if their partitioning behaviour can be determined. To quantify the partitioning and isotope fractionation factor of V between magnetite and melt, piston cylinder experiments were performed in which magnetite and a hydrous, haplogranitic melt were equilibrated at 800 °C and 0.5 GPa over a range of oxygen fugacities (\({f_{{{\text{O}}_{\text{2}}}}}\)), bracketing those of terrestrial magmas. Magnetite is isotopically light with respect to the coexisting melt, a tendency ascribed to the VI-fold V³⁺ and V⁴⁺ in magnetite, and a mixture of IV- and VI-fold V⁵⁺ and V⁴⁺ in the melt. The magnitude of the fractionation factor systematically increases with increasing log\({f_{{{\text{O}}_{\text{2}}}}}\) relative to the Fayalite–Magnetite–Quartz buffer (FMQ), from ?⁵¹V_mag-gl = ? 0.63?±?0.09‰ at FMQ ? 1 to ? 0.92?±?0.11‰ (SD) at ≈?FMQ?+?5, reflecting constant V³⁺/V⁴⁺ in magnetite but increasing V⁵⁺/V⁴⁺ in the melt with increasing log\({f_{{{\text{O}}_{\text{2}}}}}\). These first mineral-melt measurements of V isotope fractionation factors underline the importance of both oxidation state and co-ordination environment in controlling isotopic fractionation. The fractionation factors determined experimentally are in excellent agreement with those needed to explain natural isotope variations in magmatic suites. Furthermore, these experiments provide a useful framework in which to interpret vanadium isotope variations in natural rocks and magnetites, and may be used as a potential fingerprint the redox state of the magma from which they crystallise.     

Chemical composition of precipitation at Mt. Vesuvius and Vulcano Island,Italy: volcanological and environmental implications

Natural precipitation and water samples from passive devices were collected at Mt. Vesuvius and Vulcano Island, Italy, during the period 2004–2006, in order to investigate its possible interactions with fumarolic gases. Evidence of chemical reactions between fumarolic fluids and rain samples before and after its deposition into the sampling devices was found at Vulcano Island. Very low pH values (down to 2.5) and significant amounts of chlorine and sulfate (up to 22 mEq/l) were measured at sampling points located close to the fumarolic field. In contrast, anthropogenic contributions and/or dissolution of aerosols (both maritime and continental) influence the chemistry of rainwaters at Mt. Vesuvius, which show inter-annual variations that are highly consistent with those recorded at the coastal site at Vulcano Island. Chemistry of waters directly exposed to fumarolic fluids may then give useful information about its temporal evolution, holding the signal of the “maximum” chemical event occurred in the meanwhile. In addition, the observation of the health status of vegetation colonizing the immediate surroundings of the fumarolic fields, due to its strong dependence on the interactions with these fluids, may work as a possible biomarker of volcanic activity.