Distinguishing volcanic debris avalanche deposits from their reworked products: the Perrier sequence (French Massif Central)

Debris avalanches associated with volcanic sector collapse are usually high-volume high-mobility phenomena. Debris avalanche deposit remobilisation by cohesive debris flows and landslides is common, so they can share textural characteristics such as hummocks and jigsaw cracks. Distinguishing original deposits from reworked products is critical for geological understanding and hazard assessment because of their different origin, frequency and environmental impact. We present a methodology based on field evidence to differentiate such epiclastic breccias. Basal contact mapping constrained by accurate altitude and location data allows the reconstruction of deposit stratigraphy and geometry. Lithological analysis helps to distinguish the different units. Incorporation structures, kinematic indicators and component mingling textures are used to characterise erosion and transport mechanisms. We apply this method to the enigmatic sequence at Perrier (French Massif Central), where four units (U1–U4) have been interpreted either as debris flow or debris avalanche deposits. The sequence results from activity on the Monts Dore Volcano about 2 Ma ago. The epiclastic units are matrix supported with an almost flat top. U2 and U3 have clear debris flow deposit affinities such as rounded clasts and intact blocks (no jigsaw cracks). U1 and U4 have jigsaw cracked blocks with matrix injection and stretched sediment blocks. U1 lacks large blocks (>10 m wide) and has a homogenous matrix with an upward increase of trapped air vesicle content and size. This unit is interpreted as a cohesive debris flow deposit spawned from a debris avalanche upstream. In contrast, U4 has large mega-blocks (up to 40 m wide), sharp contacts between mixed facies zones with different colours and numerous jigsaw fit blocks (open jigsaw cracks filled by monogenic intra-clast matrix). Mega-blocks are concentrated near the deposit base and are spatially associated with major substratum erosion. This deposit has a debris avalanche distal facies with local debris flow affinities due to partial water saturation. We also identify two landslide deposits (L1 and L2) resulting from recent reworking that has produced a similar facies to U1 and U4. These are distinguishable from the original deposits, as they contain blocks of mixed U1/U4 facies, a distinctly less consolidated and more porous matrix and a fresh hummocky topography. This work shows how to differentiate epiclastic deposits with similar characteristics, but different origins. In doing so, we improve understanding of present and past instability of the Monts Dore and identify present landslide hazards at Perrier.     

Thermal conductive heating in fractured bedrock: Screening calculations to assess the effect of groundwater influx

A two-dimensional semi-analytical heat transfer solution is developed and a parameter sensitivity analysis performed to determine the relative importance of rock material properties (density, thermal conductivity and heat capacity) and hydrogeological properties (hydraulic gradient, fracture aperture, fracture spacing) on the ability to heat fractured rock using thermal conductive heating (TCH). The solution is developed using a Green’s function approach in which an integral equation is constructed for the temperature in the fracture. Subsurface temperature distributions are far more sensitive to hydrogeological properties than material properties. The bulk ground water influx (q) can provide a good estimate of the extent of influx cooling when influx is low to moderate, allowing the prediction of temperatures during heating without specific knowledge of the aperture and spacing of fractures. Target temperatures may not be reached or may be significantly delayed when the groundwater influx is large.     

Melting of enriched mantle beneath Pitcairn seamounts: Unusual U–Th–Ra systematics provide insights into melt extraction processes

U-series systematics as well as Sr isotopes were measured on young seamount lavas from the Pitcairn hotspot collected during the Polynaut cruise. The combined U-series and Sr isotope data reveal typical mixing relationships between two endmembers. One typical ‘plume’ endmember with radiogenic ⁸⁷Sr/⁸⁶Sr and relatively low ²³⁰Th/²³⁸U and a ‘lithosphere’ endmember with less radiogenic ⁸⁷Sr/⁸⁶Sr and relatively larger ²³⁰Th/²³⁸U. Remarkably, all the lavas, except for a few arguably older samples, are characterized by ²²⁶Ra deficits relative to ²³⁰Th. On the basis of water content and trace element systematics, we argue that this is due to melting in the presence of phlogopite, which is only stable at lithosphere temperatures. A melting model including the diffusive exchange of elements among phlogopite, garnet and melt is used to constrain melting conditions of the lithosphere. These unusual ²²⁶Ra–²³⁰Th signatures can be explained by relatively slow melting rates at low matrix porosity. Our model also demonstrates that the effective partitioning behavior is dependent on the melting rate. A simple thermal model for lithosphere heating and melting is in good agreement with predicted melting rates.     

Integration of GIS and Spatio-temporal Simulation Models: Interoperable Components for Different Simulation Strategies

New technologies for distributed object computing (DOC) challenge new approaches to integrate Geographical Information Systems (GIS) and simulation tools for spatio-temporal modeling. Several standardization initiatives work on specifying interfaces and defining service architectures for appropriate components. Currently, the most promising attempts are represented by the OpenGIS and the High Level Architecture. This paper gives a brief survey of the current state of the emerging standards, highlights the advantages and shortcomings of these attempts, and defines a possible framework for GIS-integrated simulation of spatio-temporal processes. Two abstraction layers provide interfaces for different GIS kernels and allow the integration of different simulation models. A prototype implementation of the specified interfaces shows the integration of analysis tools and two different simulation strategies: a mesoscale boundary layer model based on the Navier-Stokes equation and a cellular automata to simulate air pollutant dispersion.     

Downstream composition changes of acidic volcanic waters discharged into the Banyupahit stream, Ijen caldera, Indonesia

The crater lake of Kawah Ijen volcano contains extremely low pH (<0.4) waters with high SO₄ (70000 mg/kg), Cl (21000 mg/kg), F (1500 mg/kg), Al (5000 mg/kg), Fe (2000 mg/kg) and trace metal (Cu 0.5, Zn 4, Pb 3 mg/kg) contents. These brines seep outward through the western crater rim and reappear on the other side as streamlets, which form the headwaters of the Banyupahit stream. The Banyupahit first mixes with fresh rivers and thermal springs in the Ijen caldera and then irrigates a coastal agricultural plain which is 30 km from the summit crater.We discuss the downstream composition changes affecting the Banyupahit waters by using stable isotope, chemical and mineralogical data collected from sites along the stream length. The saturation of the stream waters with respect to minerals was evaluated with SOLVEQ and WATEQ4F and compared with the geochemical observations. An aluminous mineralogy (alunogen, pickeringite, tamarugite and kalinite) develops in the upper part of the Banyupahit due to concentration of the headwaters by evaporation. Downstream attenuation of dissolved element concentrations results principally from dilution and from mineral precipitation. The stream pH changes from 0 at the source to >4 close to the mouth. The δD and δ¹⁸O values and the relative SO₄–Cl–F contents of the Banyupahit waters indicate that the tributaries are mostly meteoric. Dissolved SO₄ in the acidic stream come only from the crater lake seepages and are not involved later in microbially mediated reactions, as shown by their δ³⁴S and δ¹⁸O values. Re-equilibration of the stream SO₄ oxygen-isotope composition with H₂O from tributaries does not occur.Calcium, SiO₂, Al, Fe, K and SO₄ behave non-conservatively in the stream waters. Gypsum, silica (amorphous or poorly ordered), a basic aluminum hydroxysulfate (basaluminite?), K-jarosite and amorphous ferric hydroxide may exert a solubility control on these elements along the entire stream length, or in certain stream sections, consistent with the thermochemical model results. Downstream concentration trends and mineral saturation levels suggest that precipitation of Sr-, Pb-rich barite and celestite consume Ba, Sr and Pb, whereas dissolved Cu, Pb and Zn may adsorb onto solid particles, especially after the junctions of the acidic stream with non-acidic rivers. We calculated that significant fluxes of SO₄, F, Cl, Al, SiO₂, Ti, Mn and Cu may reach the irrigation system, possibly causing serious environmental impacts such as soil acidification and induration.     

Electrical conductivity and crustal structure beneath the central Hellenides around the Gulf of Corinth (Greece) and their relationship with the seismotectonics

A deep magnetotelluric sounding (MTS) investigation in the western part of the Gulf of Corinth has revealed a complex electrical image of the crustal structure. The geotectonic structure of the Parnassos unit and the Transition zone in the central Hellenides, overthrusting the Pindos zone both towards the west and towards the south, has been clearly identified by its higher resistivity and its intrinsic anisotropy related to the N–S strike of the Hellenides range. Subsequent N–S extension of the Gulf introduced another heterogeneous anisotropy characteristic that corresponds to E–W-trending normal faults on both sides of the Gulf. The 2-D modelling of the MTS results reveals the existence of a relatively conductive layer about 4 km thick at a depth greater than 10 km in the middle crust. It corresponds to a ductile detachment zone suggested by microseismic and seismic studies ( King et al . 1985 ; Rigo et al . 1996 ; Bernard et al . 1997a ). It may be attributed to the phyllite series lying between the allochthonous Hellenic nappes and the autochthonous Plattenkalk basement. Towards the east, under the Pangalos peninsula, approaching the internal Hellenides, the detachment zone could root deeply into the lower crust.
Some strong local electrical anomalies are observed, reaching the conductive layer in the middle crust, such as that under the Mamousia fault and under the front of the overthrust of the Transition zone on the Pindos zone. Other anomalies affect only the shallower zones such as that beneath the Helike fault and in the Psaromita peninsula. These shallower anomalies provide complementary information to the study of spatial and temporal variations of the seismic anisotropy in relation to the short- and long-term tectonic activity of the Gulf ( Bouin et al . 1996 ; Gamar et al . 1999 ).     

Effect of Fe on garnet–melt trace element partitioning: experiments in FCMAS and quantification of crystal-chemical controls in natural systems

Garnet–melt trace element partitioning experiments were performed in the system FeO–CaO–MgO–Al₂O₃–SiO₂ (FCMAS) at 3 GPa and 1540°C, aimed specifically at studying the effect of garnet Fe²⁺ content on partition coefficients (D^Grt/Melt). D^Grt/Melt, measured by SIMS, for trivalent elements entering the garnet X-site show a small but significant dependence on garnet almandine content. This dependence is rationalised using the lattice strain model of Blundy and Wood [Blundy, J.D., Wood, B.J., 1994. Prediction of crystal–melt partition coefficients from elastic moduli. Nature 372, 452–454], which describes partitioning of an element i with radius r_i and valency Z in terms of three parameters: the effective radius of the site r₀(Z), the strain-free partition coefficient D₀(Z) for a cation with radius r₀(Z), and the apparent compressibility of the garnet X-site given by its Young's modulus E_X(Z). Combination of these results with data in Fe-free systems [Van Westrenen, W., Blundy, J.D., Wood, B.J., 1999. Crystal-chemical controls on trace element partitioning between garnet and anhydrous silicate melt. Am. Mineral. 84, 838–847] and crystal structure data for spessartine, andradite, and uvarovite, leads to the following equations for r₀(3+) and E_X(3+) as a function of garnet composition (X) and pressure (P):

r₀(3+) [Å]=0.930X_Py+0.993X_Gr+0.916X_Alm+0.946X_Spes+1.05(X_And+X_Uv)−0.005(P [GPa]−3.0)(±0.005 Å)

E_X(3+) [GPa]=3.5×10¹²(1.38+r₀(3+) [Å])^−26.7(±30 GPa)

Accuracy of these equations is shown by application to the existing garnet–melt partitioning database, covering a wide range of P and T conditions (1.8 GPa<P<5.0 GPa; 975°C<T<1640°C). D^Grt/Melt for all 3+ elements entering the X-site (REE, Sc and Y) are predicted to within 10–40% at given P, T, and X, when D^Grt/Melt for just one of these elements is known. In the absence of such knowledge, relative element fractionation (e.g. D_Sm^Grt/Melt/D_Nd^Grt/Melt) can be predicted. As an example, we predict that during partial melting of garnet peridotite, group A eclogite, and garnet pyroxenite, r₀(3+) for garnets ranges from 0.939±0.005 to 0.953±0.009 Å. These values are consistently smaller than the ionic radius of the heaviest REE, Lu. The above equations quantify the crystal-chemical controls on garnet–melt partitioning for the REE, Y and Sc. As such, they represent a major advance en route to predicting D^Grt/Melt for these elements as a function of P, T and X.     

The effect of Ca-Tschermaks component on trace element partitioning between clinopyroxene and silicate melt

We have studied the influence of Ca-Tschermaks (Calcium Tschermaks or CaTs) content of clinopyroxene on the partitioning of trace elements between this phase and silicate melt at fixed temperature and pressure. Ion probe analyses of experiments carried out in the system Na₂O–CaO–MgO–Al₂O₃–SiO₂, at 0.1 MPa and 1218°C, produced crystal-melt partition coefficients (D) of 36 trace elements (Li, Cl, Sc, Ti, V, Cr, Fe, Co, Ge, Sr, Y, Zr, Nb, Mo, Ru, Rh, In, Sn, Sb, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta and W), for clinopyroxene compositions between 10 and 32 mol% CaTs. Partition coefficients for 2+ to 5+ cations show, for each charge, a near parabolic dependence of log D on ionic radius of the substituting cation, for partitioning into both the M1 and M2 sites of clinopyroxene. Fitting the results to the elastic strain model of Blundy and Wood [Blundy, J.D., Wood, B.J., 1994. Prediction of crystal-melt partition coefficients from elastic moduli. Nature 372, 452–454] we obtain results for the strain-free partition coefficients of theoretical cations (D₀), with site radius r₀, and for the site's Young's Modulus (E).

In agreement with earlier data our results show that increasing ^ivAl concentration in cpx is matched by increasing D, E_M1, E_M2 and D₀ for tri-, tetra- and pentavalent cations. The degree of fractionation between chemically similar elements (i.e. Ta/Nb, Zr/Hf) also increases. In contrast, D values for mono-, di- and hexavalent cations decrease with increasing ^ivAl in the cpx. The large suite of trace elements used has allowed us to study the effects of cation charge on D₀, r₀ and E. We have found that D₀ and r₀ decrease with increasing cation charge, e.g. r₀=0.66 Å for 4+ cations and 0.59 Å for 5+ cations substituting into M1. Values of E_M1 and E_M2 increase with cation charge as well as with increasing ^ivAl content. The increase in E_M2 is linear and close to the trend set by Hazen and Finger [Hazen, R.M., Finger, L.W., 1979. Bulk modulus-volume relationship for cation–anion polyhedra. J. Geophys. Res. 84 (10) 6723–6728] for oxides. E_M1 values are much higher and do not fit the trend predicted by the Hazen and Finger relationship.     

Micro- and nano-textural evidence of Ti(–Ca–Fe) mobility during fluid–rock interactions in carbonaceous lawsonite-bearing rocks from New Zealand

Understanding the mobility of chemical elements during fluid–rock interactions is critical to assess the geochemical evolution of a rock undergoing burial and metamorphism and, more generally, to constrain the geochemical budget of the subduction factory. In particular, determining the behavior and mobility of Ti in aqueous fluids constitutes a great challenge that is still under scrutiny. Here, we study plant fossils preserved in blueschist metasedimentary rocks from the Marybank Formation (New Zealand). Using scanning and transmission electron microscopies (SEM and TEM), we show that the carbonaceous material (CM) composing the fossils contains abundant nano-inclusions of Ti- and Fe-oxides. These nanocrystals are mainly anatase, rutile, and Fe–Ti oxides. The mineral composition observed within the fossils is significantly different from that detected in the surrounding rock matrix. We propose that Ti and Fe might have been mobilized by the alteration of a detrital Ti–Fe-rich protolith during an early diagenetic event under acidic and reducing conditions. Aqueous fluids rich in organic ligands released by the degradation of organic matter may have been involved. Moreover, using mass balance and petrological observations, we show that the contrasted mineralogy between the rock matrix and the fossil CM might be the consequence of the chemical isolation of fossil CM during the prograde path of the rock. Such an isolation results from the early formation of quartz and Fe-rich phyllosilicate layers enclosing the fossil as characterized by SEM and TEM investigations. Overall, this study shows that investigating minerals associated with CM down to the nanometer scale in metamorphic rocks can provide a precious record of early prograde geochemical conditions.