The Role of GNSS Vertical Velocities to Correct Estimates of Sea Level Rise from Tide Gauge Measurements in Greece

In this study, we show how the Global Navigation Satellite System (GNSS)-derived vertical velocities contribute to the correction of tide gauge (TG) measurements used for the sea level rise estimation in Greece. Twelve sites with records of local sea level heights are processed in order to estimate their trend. Certain error sources related to TGs, e.g. equipment changes, data noise, may lead to biased or erroneous estimations of the sea level height. Therefore, it would be preferred to follow a robust estimation technique in order to detect and reduce outlier effects. The geocentric sea level rise is estimated by taking into account the land vertical motion of co-located GNSS permanent stations at the Hellenic area. TGs measure the height of the water relative to a monitored geodetic benchmark on land. On the other hand, using GNSS-based methods the vertical land motion can be derived. By means of extended models fitted to the GNSS time-series position, obtained from seven years of continuous data analysis, periodic signals are well described. The synergy of the two co-located techniques results in the correction of TG relative sea level heights taking into account the GNSS vertical velocities and consequently obtaining the conversion to absolute (geocentric) sea level trend.     

Analytical Solutions for Flow Fields near Drain-and-Gate Reactive Barriers

Permeable reactive barriers (PRBs) are a popular technology for passive contaminant remediation in aquifers through installation of reactive materials in the pathway of a plume. Of fundamental importance are the degree of remediation inside the reactor (residence time) and the portion of groundwater intercepted by a PRB (capture width). Based on a two-dimensional conformal mapping approach (previously used in related work), the latter is studied in the present work for drain-and-gate (DG) PRBs, which may possess a collector and a distributor drain (“full” configuration) or a collector drain only (“simple” configuration). Inherent assumptions are a homogeneous unbounded aquifer with a uniform far field, in which highly permeable drains establish constant head boundaries. Solutions for aquifer flow fields in terms of the complex potential are derived, illustrated, and analyzed for doubly symmetric DG configurations and arbitrary reactor hydraulic resistance as well as ambient groundwater flow direction. A series of practitioner-friendly charts for capture width is given to assist in PRB design and optimization without requiring complex mathematics. DG PRBs are identified as more susceptible to flow divergence around the reactor than configurations using impermeable side structures (e.g., funnel-and-gate), and deployment of impermeable walls on drains is seen to mitigate this problem under certain circumstances.     

Implications of pore space characteristics on diffusive transport in basalts and granites

A detailed characterization of the pore space is crucial for understanding of transport and element transfer in rocks. Here, the effect of differences in texture and content of secondary minerals on transport in pore systems was determined for two rocks of widespread occurrence, mid-ocean ridge basalts (MORB) and granites. Pore space characteristics were analyzed by Hg-porosimetry, intrusion of a molten alloy, and synchrotron-based X-ray tomographic microscopy. For evaluating the role of pore space characteristics for the prediction of diffusive transport, data on porosity, and the effective diffusion coefficient (D _eff) were compared. Extended connective pore systems due to cracks and mineral dissolution are present in samples of both rocks, indicating high internal specific surface area. Uneven pore size distributions in altered MORB samples can be assigned to secondary minerals. Pore spaces determined by X-ray tomography, used to determine main direction of pores in the 3-D orthogonal system, suggest a slight anisotropy. In log–log plots, both rocks show roughly a linear dependence of D _eff for H₂O and compounds with comparable diffusivities (D₂O, monovalent cations, and anions) on porosity, but at same porosity D _eff is clearly higher in granitic than in basaltic samples. This difference is increasing with decreasing porosity, indicating that at low porosities the efficiency of element transport in basaltic samples is diminished, mainly inherited by the presence of small pores slowing down diffusion. The fact that diffusive transport in basaltic rocks is stronger dependent on porosity than in granitic rocks shows that also other rock characteristics such as pore size distribution and tortuosity of the pore network, highly affected by the alteration degree, can markedly affect transport and reactivity of pore solution.     

Hydrothermalism in the Tyrrhenian Sea: Inorganic and microbial sulfur cycling as revealed by geochemical and multiple sulfur isotope data

The Palinuro volcanic complex and the Panarea hydrothermal field, both located in the Tyrrhenian Sea (Italy), are associated with island arc magmatism and characterized by polymetallic sulfide mineralization. Dissolved sulfide concentrations, pH, and Eh measured in porewaters at both sites reveal a variable hydrothermal influence on porewater chemistry.Multiple sulfur isotopic measurements for disseminated sulfides (CRS: chromium reducible sulfur) extracted from sediments at Palinuro yielded a broad range in δ³⁴S range between ?29.8 and + 10.2‰ and Δ³³S values between + 0.015 and + 0.134‰. In contrast, sediments at Panarea exhibit a much smaller range in δ³⁴S_CRS with less negative values between ?11.3 and ?1.8‰. The sulfur isotope signatures are interpreted to reflect a mixture between hydrothermal and biogenic sulfide, with a more substantial biogenic contribution at Panarea.Multiple sulfur isotope measurements were performed on sulfides and elemental sulfur from drill core material from the Palinuro massive sulfide complex. δ³⁴S and Δ³³S values for pyrite between ?32.8 and ?1.1‰ and between ?0.012 to + 0.042‰, respectively, as well as for elemental sulfur with δ³⁴S and Δ³³S values between ?26.7 and ?2.1‰ and between + 0.035 and + 0.109‰, respectively, point to a microbial origin for much of the sulfide and elemental sulfur studied. Moreover, data suggest a coupling of bacterial sulfate reduction, sulfide oxidation and sulfur disproportionation. In addition, δ³⁴S values for barite between + 25.0 and + 63.6‰ are also in agreement with high microbial turnover of sulfate at Palinuro.Although a magmatic SO₂ contribution towards the formation of the Palinuro massive sulfide complex is very likely, the activity of different sulfur utilizing microorganisms played a fundamental role during its formation. Thus, porewater and multiple sulfur isotope data reveal differences in the hydrothermal activity at Palinuro and Panarea drill sites and underline the importance of microbial communities for the origin of massive sulfide mineralizations in the hydrothermal subsurface.     

Sm-Nd,K-Ar and petrologic study of some kimberlites from eastern United States and their implication for mantle evolution

We provide new data on Sm-Nd systematics, K-Ar dating and the major element chemistry of kimberlites from the eastern United States (mostly from central New York State) and their constituent mineral phases of olivine, clinopyroxene, garnet, phlogopite and perovskite. In addition, we report Nd-isotopes in a few kimberlites from South Africa, Lesotho and from the eastern part of China. The major element compositions of the New York dike rocks and of their constituent minerals including a xenolith of eclogite are comparable with those from the Kimberley area in South Africa. The K-Ar age of emplacement of the New York dikes is further established to be 143 Ma.We have analyzed the Nd-isotopic composition of the following kimberlites and related rocks: Nine kimberlite pipes from South Africa and Lesotho, two from southern India; one from the U.S.S.R., fifteen kimberlite pipes and related dike rocks from eastern and central U.S. and two pipes from the Shandong Province of eastern China. The age of emplacement of these kimberlites ranges from 1300 million years to 90 million years. The initial Nd-isotopic compositions of these kimberlitic rocks expressed as _Nd ^I with respect to a chondritic bulk-earth growth-curve show a range between 0 and +4, with the majority of the kimberlites being in the range 0 to +2. This range is not matched by any other suite of mantle-derived igneous rocks. This result strengthens our earlier conclusion that kimberlitic liquids are derived from a relatively primeval and unique mantle reservoir with a nearly chondritic Sm/Nd ratio.     

Water and the density of silicate glasses

A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm³/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10–20 kbar pressures and containing up to 7 wt% H₂O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO₂–M₂O systems (M=H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H₂O is about 4 × 10⁻⁵ K⁻¹ in silicate glasses. Received: 30 June 1999 / Accepted: 5 November 1999