Constraining Holocene sea levels using U‐Th ages of phreatic overgrowths on speleothems from coastal caves in Mallorca (Western Mediterranean)

Phreatic overgrowths on speleothems (POS) are carbonate formations deposited at the water table of caves in unique karstic coastal settings having morphologies that can be directly related to sea level at the time of formation. The U‐Th ages of calcite and aragonite overgrowths collected from the modern water table in coastal caves on Mallorca (Cova de Cala Varques A and Cova des Pas de Vallgornera) were determined using high‐precision MC‐ICPMS techniques. U‐Th ages indicate that phreatic carbonate deposition occurred between ca 2·8 and at least 0·6 ka BP and are in accord with an archeologically estimated age of 3·7–3·0 ka BP for a drowned prehistoric construction at a depth of 1 m below current sea level in a cave from the same area. Speleothem δ¹³C and δ¹⁸O and chemical composition of cave pools provide supportive evidence that POS reflect mixing between seawater and brackish water table. Copyright © 2010 John Wiley & Sons, Ltd.     

MAJOR AND TRACE ELEMENT DETERMINATIONS ON NIST GLASS STANDARD REFERENCE MATERIALS 611, 612, 614 AND 1834 BY INDUCTIVELY COUPLED PLASMA-MASS SPECTROMETRY

We report on the major and trace element composition and homogeneity of NIST (National Institute of Standards and Technology) glass standard reference materials 611, 612, 614, and 1834 for use as microanalytical trace element standards in laser ablation-inductively coupled plasma-mass spectrometry. The four analyzed NIST glasses were not designed as microanalytical standards, but their availability and careful preparation made them obvious candidates. Our data indicate that NIST 1834 is inhomogeneous on a scale of 100 mg with respect to several trace elements. Within analytical uncertainty, NIST 611, 612, and 614 are apparently homogeneous.     

TRACE ELEMENT DETERMINATIONS FOR USGS BASALT BHVO-1 AND NIST STANDARD REFERENCE MATERIALS 278, 688 AND 694 BY INDUCTIVELY COUPLED PLASMA-MASS SPECTROMETRY

Results are presented for 26 to 30 trace elements determined in four rock reference materials of geochemical interest: USGS Basalt BHVO-1, Rhyolite Obsidian NIST 278, Basalt NIST688, and Phosphate Rock NIST694. Determinations were made by inductively coupled plasma mass spectrometry (ICP-MS). Good agreement was obtained among solution standard comparison and standard addition analytical techniques, and among samples prepared with different dissolution methods. Generally good agreement was obtained between determined trace element values and values reported in the literature.     

Measurement of copper release rates from antifouling paint under laboratory and in situ conditions: implications for loading estimation to marine water bodies

The release of biocides, such as copper (Cu), from antifouling (AF) coatings on vessel hulls represents a significant proportion of overall Cu loading in those harbors and estuaries where substantial numbers of small craft or large vessels are berthed. Copper release rates were measured on several self-polishing, tin-free coatings and an ablative Cu reference coating applied to steel panels using three measurement methods. The panels were exposed in natural seawater in San Diego Bay, and release rates were measured both in the laboratory and field over 2 years. Results with the static (20 cm x 30 cm) panels indicated that Cu release rates were initially high (25-65 microg Cu cm(-2)day(-1)), with a large range of values between paint types. Release rates declined to substantially lower rates (8-22 microg cm(-2)day(-1)) with reduced variability within 2 months. Release rates continued to decrease over time for approximately 6 months when relatively constant release rates were observed for most coatings. Over time, relative differences in Cu release rates measured by three exposure methods decreased, with all coatings exhibiting similar behavior toward the end of the study. Lowest overall Cu release rates were observed with the self-polishing experimental paint no. 7 in static-dynamic and in situ treatments. The highest periodic release rates were measured from panels that experienced periods of both static and dynamic exposure (8.7 ms(-1) rotation). The lowest release rates were measured from panels that experienced static, constant depth exposure, and where release rates were evaluated in situ, using a novel diver-deployed measurement system. Results from this in situ technique suggests that it more closely reflects actual Cu release rates on vessel hulls measured with intact natural biofilms under ambient conditions than measurements using standardized laboratory release rate methods. In situ measurements made directly on the AF surface of vessels demonstrated typically lower release rates than from the panel studies, averaging 8.2 microg cm(-2)day(-1) on pleasure craft, and 3.8 microg cm(-2)day(-1) on Navy vessels. The data suggest that the presence of an established biofilm likely serves to moderate the release of Cu from field-exposed antifouling coatings both on panels and hull surfaces.     

Cu isotopic fractionation in the supergene environment with and without bacteria

The isotopic composition of dissolved Cu and solid Cu-rich minerals [δ⁶⁵Cu (‰) = (⁶⁵Cu/⁶³Cu_sample/⁶⁵Cu/⁶³Cu_std) - 1)*1000] were monitored in batch oxidative dissolution experiments with and without Thiobacillus ferrooxidans. Aqueous copper in leach fluids released during abiotic oxidation of both chalcocite and chalcopyrite was isotopically heavier (δ⁶⁵Cu = 5.34‰ and δ⁶⁵Cu = 1.90‰, respectively, [±0.16 at 2σ]) than the initial starting material (δ⁶⁵Cu = 2.60 ± 0.16‰ and δ⁶⁵Cu = 0.58 ± 0.16‰, respectively). Isotopic mass balance between the starting material, aqueous copper, and secondary minerals precipitated in these experiments explains the heavier isotopic values of aqueous copper. In contrast, aqueous copper from leached chalcocite and chalcopyrite inoculated with Thiobacillus ferrooxidans was isotopically similar to the starting material. The lack of fractionation of the aqueous copper in the biotic experiments can best be explained by assuming a sink for isotopically heavy copper present in the bacteria cells with δ⁶⁵Cu = 5.59 ± 0.16‰. Consistent with this inference, amorphous Cu-Fe oxide minerals are observed surrounding cell membranes of Thiobacillus grown in the presence of dissolved Cu and Fe.Extrapolating these experiments to natural supergene environments implies that release of isotopically heavy aqueous Cu from oxidative leach caps, especially under abiotic conditions, should result in precipitates in underlying enrichment blankets that are isotopically heavy. Where iron-oxidizing cells are involved, isotopically heavy oxidized Cu entrained in cellular material may become associated with leach caps, causing the released aqueous Cu to be less isotopically enriched in the heavy isotope than predicted for the abiotic system. Rayleigh fractionation trends with fractionation factors calculated from our experiments for both biotic and abiotic conditions are consistent with large numbers of individual abiotic or biotic leaching events, explaining the supergene chalcocites in the Morenci and Silver Bell porphyry copper deposits.     

Nd-Sr isotope composition of lower crustal xenoliths — Evidence for the origin of mid-tertiary felsic volcanics in Mexico

Isotopic data were collected on lower crustal xenoliths to constrain the Mexican lower crust as source material for the mid-Tertiary Sierra Madre Occidental, which is one of the largest silicic volcanic piles known. The xenoliths are predominantly pelitic gneisses and mafic orthogneisses that were brought to the surface on the eastern edge of the Sierra Madre Occidental by recent alkalic basalts. The pelitic gneisses are uniform in mineral assemblage and contain garnet+quartz+plagioclase+sanidine+rutile +sillimanite/kyanite+graphite. The orthogneisses are plagioclase, garnet and/or spinel bearing two pyroxene granulites. Available geothermometric and geobarometric data show that the xenoliths equilibrated at temperatures and pressures consistent with those of the mantle/crust boundary in those areas.The xenoliths range from 46.2 to 67.2 SiO₂. Paragneisses are in general more silicic than the orthogneisses. The xenoliths have Rb concentrations between 0.4 and 97 ppm but most samples are very low, with less than 3 ppm Rb. The Sr isotopic ratios of orthogneisses from the lowermost crust throughout most of northern Mexico are very similar and range from ca. 0.705 to 0.706. Previous studies indicate that these rocks have measured (inNd) values between+2 and –5. Paragneiss xenoliths are generally more radiogenic in Sr isotopic ratio, up to 0.730, and have lower _Nd values of–11.The Nd and Sr isotopic characteristics of the orthogneisses are similar to those of the voluminous mid-Tertiary ignimbrites of the Sierra Madre Occidental. The xenoliths cannot represent cumulate material produced during the mid-Tertiary volcanism because they are Paleozoic or older. Consequently, based on Sr and Nd isotopic data, the silicic ignimbrites could comprise up to 100% lower crustal material.     

A Location Aware Mobile Tool for Direct and Indirect Climate Data Sensors

Access to GIS data from mobile platforms continues to be a challenge and there is a wide range of fields where it is extremely useful. In this work, we combined three key aspects: climate data sensors, mobile platforms and spatial proximity operations. We published and made use of a web 2.0 network of climate data, where content is user‐collected, by means of their meteorological stations, and exposed as available information for the virtual community. Moreover, we enriched this data by giving the users the opportunity to directly inform the system with different climate measures. In general, management of this type of information from a mobile application could result in an important decision tool, as it enables us to provide climate‐related data according to a context and a geographical location. Therefore, we implemented a native mobile application for iPhone and iPad platforms by using ArcGIS SDK for iOS and by integrating a series of ArcGIS webmaps, which allows us to perform geospatial queries based on the user's location, offering, at the same time, access to all the data provided by the climate data sensor network and from direct users.     

Molybdenite Mineralization and Re‐Os Geochronology of the Escondida and Escondida Norte Porphyry Deposits,Northern Chile

Molybdenum is an economically important subproduct of North Chilean porphyry‐type deposits, and thus spatial and temporal distribution of molybdenite as the primary Mo‐bearing mineral in the Escondida and Escondida Norte deposits were characterized using several mineralogical and chemical techniques and the Re‐Os dating method. Molybdenum is distributed extensively in the two deposits, and high molybdenum concentrations (>500 ppm) are recognized particularly in the chlorite‐sericite transitional zone between the potassic and sericitic zones. Two modes of occurrence of molybdenite are observed in the Escondida deposit: aggregates with Cu‐Fe‐sulfide minerals in fine veinlets (sulfide‐veinlet type), and monomineralic microveinlets associated with NE‐trending faults. The former and the latter yielded ages of 36.1 ± 0.2 Ma and 35.2 ± 0.2 Ma, respectively. Re‐Os dating of Escondida Norte molybdenites also show two distinct episodes, at 37.7 ± 0.3 Ma and a younger episode at 36.6 ± 0.2 Ma. These data indicate that the Escondida Norte is older than the main Escondida deposit. The Re‐Os age data combined with those of the porphyry emplacement suggest that the molybdenite mineralization in the Escondida district occurred as several short episodic pulses during the late‐magmatic to hydrothermal transition, and that the Cu‐Mo deposits were formed in a variable overall period spanning 1 to 5 m.y.     

Wind influence on surface current variability in the Ibiza Channel from HF Radar

Surface current variability is investigated using 2.5 years of continuous velocity measurements from an high frequency radar (HFR) located in the Ibiza Channel (Western Mediterranean Sea). The Ibiza Channel is identified as a key geographical feature for the exchange of water masses but still poorly documented. Operational, quality controlled, HFR derived velocities are provided by the Balearic Islands Coastal Observing and Forecasting System (SOCIB). They are assessed by performing statistical comparisons with current-meter, ADCP, and surface lagrangian drifters. HFR system does not show significant bias, and its accuracy is in accordance with previous studies performed in other areas. The main surface circulation patterns are deduced from an EOF analysis. The first three modes represent almost 70 % of the total variability. A cross-correlation analysis between zonal and meridional wind components and the temporal amplitudes of the first three modes reveal that the first two modes are mainly driven by local winds, with immediate effects of wind forcing and veering following Ekman effect. The first mode (37 % of total variability) is the response of meridional wind while the second mode (24 % of total variability) is linked primarily with zonal winds. The third and higher order modes are related to mesoscale circulation features. HFR derived surface transport presents a markedly seasonal variability being mostly southwards. Its comparison with Ekman-induced transport shows that wind contribution to the total surface transport is on average around 65 %.