On the lack of a unique relation between CO2 partial pressure and temperature in geothermal system. Comment on “Geothermal mineral equilibria” by W. F. Giggenbach

Giggenbach (1981) has proposed a relation of van't Hoff form, log₁₀P_CO2 = A ? B/(t + 273), between temperature and CO₂ partial pressure in deep liquid in geothermal systems. The proposed values for the coefficients are A = 15.26, B = 7850.The proposal is not supported by pressure-temperature data used by Giggenbach, and a survey of different fields indicates that the proposal is not valid.     

An efficient forward model of the climate controls on interannual variation in tree-ring width

We present a simple, efficient, process-based forward model of tree-ring growth, called Vaganov–Shashkin-Lite (VS-Lite), that requires as inputs only latitude and monthly temperature and precipitation. Simulations of six bristlecone pine ring-width chronologies demonstrate the interpretability of model output as an accurate representation of the climatic controls on growth. Ensemble simulations by VS-Lite of two networks of North American ring-width chronologies correlate with observations at higher significance levels on average than simulations formed by regression of ring width on the principal components of the same monthly climate data. VS-Lite retains more skill outside of calibration intervals than does the principal components regression approach. It captures the dominant low- and high-frequency spatiotemporal ring-width signals in the network with an inhomogeneous, multivariate relationship to climate. Because continuous meteorological data are most widely available at monthly temporal resolution, our model extends the set of sites at which forward-modeling studies are possible. Other potential uses of VS-Lite include generation of synthetic ring-width series for pseudo-proxy studies, as a data level model in data assimilation-based climate reconstructions, and for bias estimation in actual ring-width index series.     

Petrologic and experimental evidence for the movement and heating of the pre-eruptive Minoan rhyodacite (Santorini, Greece)

Hydrothermal experiments combined with petrologic observations form the basis for a new two-stage model for the evolution of the pre-eruption Minoan magma chamber at Santorini, Greece. Ninety-nine percent of the erupted volume is two-pyroxene, rhyodacitic magma that had been stored at a temperature of ∼885 °C, based on magnetite-ilmenite and QUILF geothermometry. The rest of the volume is basaltic to andesitic magma, which occurs as <10 cm scoria clasts and as small inclusions in rhyodacite pumices. Petrologic observations show that these magmas mixed at different scales and at different times (i.e., multiple batches of mafic magma). Hydrothermal experiments were carried out on samples of rhyodacite and a mafic scoria in order to determine magma storage conditions and the mixing history of the two magmas. At 885 °C, the rhyodacite must have been stored at water-saturated pressures of ∼50 MPa, based on its phase assemblage, matrix-glass composition, and crystal content. However, glass inclusions inside rhyodacitic plagioclase phenocrysts contain more than 6 wt% H₂O, indicating they formed at pressures >200 MPa. In addition, the composition of the plagioclase hosts (An_{56 ± 6}) of the inclusions require temperatures of 825 ± 25 °C at pressures >200 MPa. This demonstrates that the Minoan rhyodacitic magma underwent a two-stage evolution, first crystallizing at ∼825^∘C and >200 MPa, and then rinsing to a shallow ∼50 MPa storage region with a concomitant rise in temperature to ∼885 °C. We suggest that the episodic intrusion of mafic magmas provided the necessary heat and perhaps contributed to the ascent of the magma to shallow crustal depths where it reequilibrated before the cataclysmic eruption. Phase equilibria suggest that much of the heating of the rhyodacite occurred in the shallow storage region. Thermal budget calculations suggest that the rhyodacite magma could have been heated by intrusions of basalt rising at reasonable upwelling rates and injected into the storage zone over several hundred years. Preservation of amphibole in the mafic scoria indicate that injection of mafic magma continued up until days before the cataclysmic eruption, perhaps triggering the event. Received: 30 September 1997 / Accepted: 5 October 1998     

Dating Quaternary volcanism and incision by the River Tigris at Diyarbakır,southeast Turkey

New high‐precision Ar‐Ar dating of basalt underlying the city of Diyarbak?r, southeast Turkey, constrains the Quaternary incision history of the River Tigris, strengthening the pre‐existing chronology based on magnetostratigraphy and K‐Ar dates. The basalt, which overlies Tigris terrace gravel 70 m above the river, is part of the Karacada? shield volcano complex centred ca. 60 km to the southwest. The reverse‐magnetised Diyarbak?r basalt, one of relatively few flow units to reach the Tigris valley axis, has been dated to 1196 ± 19 ka (±2σ). Two lower terraces have been recognised in the Diyarbak?r area, 46 and 32 m above the present river, with at least one other further downstream. From this evidence the rate of Middle‐Late Pleistocene incision by the Tigris can be estimated; it probably reached ca. 0.07 mm a^?1, reflecting the characteristic global increase in uplift rates observed at that time. Copyright © 2007 John Wiley & Sons, Ltd.     

Graphite oxidation in the Apollo 17 orange glass magma: Implications for the generation of a lunar volcanic gas phase

An Apollo 17 picritic orange glass composition has been used to experimentally investigate the conditions at which graphite would oxidize to form a CO-rich gas, and ultimately produce lunar fire-fountain eruptions. Isothermal decompression experiments run above the A17 orange glass liquidus temperature (>1350 °C) suggest that the initial CO-rich gas phase produced by graphite oxidation would be generated during magma ascent at a pressure of 40 MPa, 8.5 km beneath the lunar surface. Additional experiments with 2000 ppm S and 1000 ppm Cl showed that the presence of these dissolved gas species would not affect the depth of graphite oxidation, verifying that the first volcanic gas phase would be generated by the oxidation of graphite.A simple ideal chemical mixing model for calculating melt FeO activity in a Fe-metal/silicate melt system was tested with a series of 0.1 MPa controlled oxygen fugacity experiments. Agreement between the model and experiments allows the model to be used to calculate oxygen fugacity in picritic lunar glass compositions such as the A17 orange glass. Using this model in a reanalysis of chemical equilibria between the natural A17 orange glass melt and the metal spherules (Fe₈₅Ni₁₄Co₁) trapped within the glass beads indicates a log oxygen fugacity of −11.2, 0.7 log units, more oxidized than previous estimates. At the A17 orange glass liquidus temperature (1350 ± 5 °C), this f_O2 corresponds to a minimum pressure of 41 MPa on the graphite–C–O surface. The fact that the same critical graphite oxidation pressure was determined in decompression experiments and from the Fe–FeO activity model for the natural A17 orange glass–metal assemblage strongly supports this pressure (8.5 km depth) for volcanic gas formation in lunar basalts. Generation of a gas by oxidation of C in ascending magma is likely to have been important in getting dense lunar magmas to the surface as well as in generating fire-fountain eruptions. The vesicles common in many lunar basalts and the ubiquitous Fe-metal in these rocks are also likely generated by the oxidation of carbon. The presence of carbon in the lunar basalts and the recent discovery of ppm levels of water in lunar basalts indicate that at least parts of the lunar interior still contained volatiles at 3.9 bybp.     

Stereo-Photogrammetric Mapping of Tooth Replicas Incorporating Texture

Commercial digital photogrammetric software has been applied to convergent stereoscopic photography of human tooth replicas prepared to exhibit optical texture resulting in successful generation of 3D coordinate data. Tooth replicas were imaged using a semi-metric 35 mm camera and f = 100 mm macro lens on extension bellows. Model precision was within acceptable limits of 12  μ m or better for manual target matching and 21  μ m or better for automatic image matching. Further improvement in optical texture is required to achieve automatic image matching precision comparable to that of manual target matching. Small errors in interior orientation parameters attributed to instability in the bellows as well as small errors in the relative orientation resulted in some systematic errors. The use of a fixed camera lens system is expected to reduce these errors. When combined with commercially available, moderately priced, digital SLR cameras this brings 3D model generation closer to everyday clinical dental practice.     

Hydrochemical and isotopic characterisation of groundwaters to define aquifer type and connectivity in a subtropical coastal setting,Fraser Coast,Queensland

Physico-chemical parameters, major ion chemistry and isotope composition of surface and groundwaters were determined in forested coastal catchments and adjacent coastal plains. Results showed obvious characterisation related to physical and hydrological setting, and highly variable spatial differences reflecting the complexities of these areas. All these coastal waters are dominated by Na–Cl and fall on a common dilution line; hydrochemical grouping is largely due to anionic differences (Cl, SO₄ and HCO₃), although Na and Mg ratios also vary. Six major hydrochemical facies were determined. For groundwaters, compositional differences are largely related to aquifer material and level of confinement; for coastal groundwaters important are tidal effects and proximity to the shoreline. Differentiation for surface waters is mainly by drainage morphology, flow regime plus proximity to the coast. Connectivity between water bodies is reflected by minor base flow to catchment streams, including with flood plain wetlands, but mostly occurs in low-lying zones where there is mixing of fresh and saline water within surface water and subterranean estuaries, or by seawater intrusion enhanced by overuse. Oxygen and hydrogen isotopic data for confined and semi-confined groundwaters along the coast indicates local recharge; fresh surface waters in the elevated catchments are shown to be sourced further inland plus have experienced evaporation.     

Water–Rock Interactions: An Investigation of the Relationships Between Mineralogy and Groundwater Composition and Flow in a Subtropical Basalt Aquifer

A holistic study of the composition of the basalt groundwaters of the Atherton Tablelands region in Queensland, Australia was undertaken to elucidate possible mechanisms for the evolution of these very low salinity, silica- and bicarbonate-rich groundwaters. It is proposed that aluminosilicate mineral weathering is the major contributing process to the overall composition of the basalt groundwaters. The groundwaters approach equilibrium with respect to the primary minerals with increasing pH and are mostly in equilibrium with the major secondary minerals (kaolinite and smectite), and other secondary phases such as goethite, hematite, and gibbsite, which are common accessory minerals in the Atherton basalts. The mineralogy of the basalt rocks, which has been examined using X-ray diffraction and whole rock geochemistry methods, supports the proposed model for the hydrogeochemical evolution of these groundwaters: precipitation + CO₂ (atmospheric + soil) + pyroxene + feldspars + olivine yields H₄SiO₄, HCO₃ ⁻, Mg²⁺, Na⁺, Ca²⁺ + kaolinite and smectite clays + amorphous or crystalline silica + accessory minerals (hematite, goethite, gibbsite, carbonates, zeolites, and pyrite). The variations in the mineralogical content of these basalts also provide insights into the controls on groundwater storage and movement in this aquifer system. The fresh and weathered vesicular basalts are considered to be important in terms of zones of groundwater occurrence, while the fractures in the massive basalt are important pathways for groundwater movement.     

Mitigation of greenhouse gas emissions from land use: creating incentives within greenhouse gas emissions trading systems

Terrestrial carbon sinks and sources were introduced into climate change mitigation related policy relatively late in the design of the architecture of those policies. Much literature addresses how terrestrial sources and sinks differ from emissions from fossil fuel combustion and, hence, is a possible justification for differential treatment of them in policy design. Late introduction in climate policy discussions and perceived differences appear to have resulted in very different policy approaches for sinks versus fossil emission sources. The attempt to differentiate has generated complexity in policy design and likely inefficiency in the operation of these policies. We review these issues and find that the characteristics claimed to apply to sinks apply as well to fossil sources, and differences that do exist are often more a matter of degree than of kind. Because cap-and-trade has gained momentum as the instrument of choice to control fossil emissions, we use as a starting point, how such a cap-and-trade system could be altered to include terrestrial carbon sinks and sources.     

Isotope hydrology of the Allt a' Mharcaidh catchment,Cairngorms, Scotland: implications for hydrological pathways and residence times

The hydrology of oxygen‐18 (¹⁸O) isotopes was monitored between 1995 and 1998 in the Allt a' Mharcaidh catchment in the Cairngorm Mountains, Scotland. Precipitation (mean δ¹⁸O=−7·69‰) exhibited strong seasonal variation in δ¹⁸O values over the study period, ranging from −2·47‰ in the summer to −20·93‰ in the winter months. As expected, such variation was substantially damped in stream waters, which had a mean and range of δ¹⁸O of −9·56‰ and −8·45 to −10·44‰, respectively. Despite this, oxygen‐18 proved a useful tracer and streamwater δ¹⁸O variations could be explained in terms of a two‐component mixing model, involving a seasonally variable δ¹⁸O signature in storm runoff, mixing with groundwater characterized by relatively stable δ¹⁸O levels. Variations in soil water δ¹⁸O implied the routing of depleted spring snowmelt and enriched summer rainfall into streamwaters, probably by near‐surface hydrological pathways in peaty soils. The relatively stable isotope composition of baseflows is consistent with effective mixing processes in shallow aquifers at the catchment scale. Examination of the seasonal variation in δ¹⁸O levels in various catchment waters provided a first approximation of mean residence times in the major hydrological stores. Preliminary estimates are 0·2–0·8 years for near‐surface soil water that contributes to storm runoff and 2 and >5 years for shallow and deeper groundwater, respectively. These ¹⁸O data sets provide further evidence that the influence of groundwater on the hydrology and hydrochemistry of upland catchments has been underestimated. Copyright © 2000 John Wiley & Sons, Ltd.