Relationships between seep-carbonates,mud volcanism and basin geometry in the Late Miocene of the northern Apennines of Italy: the Montardone mélange

The Montardone mélange (Mm) is a chaotic, block-in-matrix unit outcropping in the Montebaranzone syncline in the northern Apennines. The Mm occurs in the uppermost part of the Termina Fm, the Middle–Late Miocene interval of a succession deposited in a wedge-top slope basin (Epiligurian succession). The Mm is closely associated with bodies of authigenic carbonates, characterized by negative values of δ¹³C (from ?18.22 to ?39.05 ‰ PDB) and chemosynthetic benthic fauna (lucinid and vesicomyid bivalves). In this paper, we propose that the Mm is a mud volcano originated by the post-depositional reactivation and rising of a stratigraphically lower mud-rich mass transport body (Canossa–Val Tiepido sedimentary mélange or olistostrome) triggered by fluid overpressure. We base our conclusion on (1) the Mm pierces the entire Termina Fm and older Epiligurian units and represents the direct continuation of the underlying Canossa–Val Tiepido mélange; (2) the geometry and facies distribution of the Montebaranzone sandstone body, which are compatible with a confined basin controlled by the rising of the Mm; (3) the systematic presence of large-scale (lateral extension 300–400 m) seep-carbonates associated with the mélange, suggesting a persistent gas-enriched fluid vent from the ascending overpressured mud; (4) blocks and clasts sourced from the Mm, hosted by the authigenic carbonates, conveyed by ascending mud and gas-enriched fluids. The Mm represents one of the few fossil examples of reactivation of a basin-scale sedimentary mélange (olistostrome); a three-stage model showing mechanisms of Mm raising is proposed.     

Estimating the hydraulic properties of an aquitard from in situ pore pressure measurements

A workflow is described to estimate specific storage (S _s) and hydraulic conductivity (K) from a profile of vibrating wire piezometers embedded into a regional aquitard in Australia. The loading efficiency, compressibility and S _s were estimated from pore pressure response to atmospheric pressure changes, and K was estimated from the earliest part of the measurement record following grouting. Results indicate that S _s and K were, respectively, 8.8?×?10^?6 to 1.2?×?10^?5 m^?1 and 2?×?10^?12 m s^?1 for a claystone/siltstone, and 4.3?×?10^?6 to 9.6?×?10^?6 m^?1 and 1?×?10^?12 to 5?×?10^?12 m s^?1 for a thick mudstone. K estimates from the pore pressure response are within one order of magnitude when compared to direct measurement in a laboratory and inverse modelled flux rates determined from natural tracer profiles. Further analysis of the evolution and longevity of the properties of borehole grout (e.g. thermal and chemical effects) may help refine the estimation of formation hydraulic properties using this workflow. However, the convergence of K values illustrates the benefit of multiple lines of evidence to support aquitard characterization. An additional benefit of in situ pore pressure measurement is the generation of long-term data to constrain groundwater flow models, which provides a link between laboratory scale data and the formation scale.     

Stability of equilibrium solutions in the critical case of even-order resonance in periodic Hamiltonian systems with one degree of freedom

The stability in the Lyapunov sense of an equilibrium position in a periodic Hamiltonian system with one degree of freedom is studied. It is assumed that the equilibrium is stable in the first approximation and that there exists an even resonance of order $k$ k , arbitrary. The critical case is considered, i.e., when the system of parameters is such that, in order to draw rigorous conclusions about the stability of the equilibrium position in the Lypaunov sense, terms or order higher than three in the series expansion of the Hamiltonian function must be taken into account. Sufficient conditions are derived for stability and instability.     

The caranto paleosol and its role in the early urbanization of Venice

As rising sea level threatens Venice, there is a need to construct a historical framework for interpreting modern environmental changes. Environmental conditions that would later help support Venice's urbanization were established during the Late Glacial period when calcic soils began to develop in the Venetian alluvial paleoplain. A calcic paleosol, buried by Middle to Late Holocene marine transgressive deposits, represents a subsurface layer long known in the Venice area as “caranto.” Referenced in the ancient chronicles of architects and builders, the caranto exhibits relatively high compressive and shear strength, making it an important substrate for supporting building foundations, some dating back to the Gothic era (12th–15th centuries A.D.). Hence, the caranto paleosol documents local post‐glacial environmental changes while playing an important role in Venetian building construction and human settlement. Here we provide geochemical, sedimentological, paleoecological, and chronological analyses of the caranto paleosol and related deposits based on recent coring of the Venetian Lagoon. © 2011 Wiley Periodicals, Inc.     

The Colônia structure,São Paulo,Brazil

Abstract– The near‐circular Colônia structure, located in the southern suburbs of the mega‐city of São Paulo, Brazil, has attracted the attention of geoscientists for several decades due to its anomalous character and the complete absence of any plausible endogenous geologic explanation for its formation. Origin by impact cratering has been suggested repeatedly since the 1960s, but no direct evidence for this has been presented to date. New seismic data have been recently acquired at Colônia, providing new insights into the characteristics and possible layering of infill of the structure, as well as into the depth to the underlying basement. We review the current knowledge about the Colônia structure, present the new seismic data, and discuss the existing—as yet still indirect—evidence for a possible origin by an impact. The new data suggest the existence of a sedimentary fill of approximately 275 m thickness and also the presence of two intermediate zones between sediment and basement: an upper zone that is approximately 65 m thick and can be interpreted as a possible crater‐fill breccia, whereas the other zone possibly represents fractured/brecciated basement, with a thickness of approximately 50 m. Although this depth to basement seems to be inconsistent with the expected geometry of a simple, bowl‐shape impact structure of such diameter, there are a number of still unconstrained parameters that could explain this, such as projectile nature, size and velocity, impact angle, and particularly the current erosion depth.     

Chemostratigraphy of Mesoproterozoic and Neoproterozoic carbonates of the Nico Pérez Terrane,Río de la Plata Craton,Uruguay

Increasing evidence shows that Mesoproterozoic rocks are widespread in the Río de la Plata Craton. Carbon and strontium isotope analyses were carried out for three different, carbonate-bearing successions in the southern Nico Pérez Terrane. The Parque UTE Group is erected, comprising (from base to top) the mainly volcanogenic Cañada Espinillo Formation, the dolomitic Mina Valencia Formation and the mixed carbonate-siliciclastic Cerro del Mástil Formation. A δ¹³C curve was obtained for carbonates of the Parque UTE Group, which is characterized by a plateau at +1 to +1.6‰ V-PDB, bracketed between two negative excursions (−1.8‰ V-PDB at the base and −3.3‰ V-PDB at the top). These values are consistent with a Mesoproterozoic depositional age for the unit, as indicated by U–Pb ages of synsedimentary volcanics and gabbros of 1429 ± 21 and 1492 ± 4 Ma, respectively.     

The action of neutral oleic acid in the flotation of hematite

Acidification of solutions of oleate salts forms emulsions of oleic acid. It was found that these emulsions produce a different adsorption behaviour on different size fractions of the same mineral. At low oleate concentrations, for the finer fractions, adsorption at acid pH was higher than chemisorption at pH = 7.5; adsorption was lower for the coarser, flotation-size fractions. Therefore, the conclusions obtained in acid solutions for the adsorption of oleate on fine minerals cannot be applied to flotation-size minerals.At low oleate concentrations there is a good correlation between oleate adsorption and hematite flotation. This does not hold for oleate concentrations > 5· 10^?5M, where there is poor flotability in the acid region, although the adsorption of oleic acid is very high. This is attributed to the disordered character of the layer of cooperatively adsorbed oleic acid.