Geochemical correlations between effusive and explosive silicic volcanics in the Saraykent region (Yozgat), central Anatolia,Turkey

Two main volcanic events are distinguished between Saraykent and Akçakışla in the Yozgat province of central Anatolia: (1) early Late Cretaceous–Palaeocene effusive activity, that produced a sequence of intermediate to felsic ‘basal lavas’; and (2) marginally later Palaeocene explosive activity that formed a series of covering ignimbrite flows. Due to their close temporal and spatial relation, geochemical comparisons were made between the silicic members of the lavas and ignimbrites, to identify chemical groups and their relative petrogenesis. The basal lavas range from calc‐alkaline basaltic andesites to dominant rhyolites. Based on trace element correlations three main geochemical groups were identified: the Akçakışla rhyolites (present as domes); Akçakışla rhyodacites‐dacites (lava flows); and Ozan‐Saraykent rhyolites (lava flows). Large‐ion lithophile elements have been mobile in all the groups, but mainly in the Akçakışla rhyolites. Rare earth element (REE) patterns show marked similarity between the Ozan and Saraykent basal lavas. The Akçakışla dome rhyolites are more fractionated with lower La_N/Yb_N ratios (c.10), whereas the Akçakışla basal lavas have much higher La_N/Yb_N ratios (c.30). The chemical coherence and petrographic similarities between the Saraykent and Ozan lavas suggest a single suite related via fractionation. Three geochemical groups were also established for the ignimbrites: Saraykent ignimbrite; Bağlıca ignimbrite‐Toklu‐Kızıldağ crystal tuffs; and Keklikpınar ignimbrite. The ignimbrites, like the basal lavas, display a pronounced depletion in Ba on ORG‐normalized plots. Relative to the basal lavas, chondrite‐normalized patterns for the ignimbrites are different in displaying negative Eu anomalies that indicate feldspar fractionation. The lack of geochemical overlap or coherence between any of the lava and ignimbrite groups suggests that they represent distinct eruptive events and are not related in any simple volcanic development and cogenetic sense. Two geochemical features are common to all the volcanic rock groups: (1) the presence of a Nb‐Ta anomaly, which is generally accepted as a crustal signature; and (2) the relatively low Y abundances which appear characteristic for the region as a whole. These fundamental features of the local silicic volcanism largely reflect source composition and effects. Copyright © 2002 John Wiley & Sons, Ltd.     

Sea-level rise impacts on longitudinal salinity for a low-gradient estuarine system

Climatic Change - Salinity response to sea-level rise is evaluated for a low-gradient, tidally active estuary, the lower St. Johns River, Florida. A high-resolution numerical model is forced by...     

Experimental determination of carbon isotope fractionation between CaCO3 and graphite

Carbon isotopic exchange between graphite and three polymorphs of CaCO₃ was investigated at temperatures of 600-1400 °C and at pressures from 1.4 to 2.3 GPa. Fractionation factors at all temperatures were determined by the partial exchange treatment of Northrop and Clayton (1966).Graphite starting material for the majority of the experiments was milled in water for 20-25 h, producing aggregates of nanosheets. The sheets range in width from 50 to 1000 nm and in thickness from 20 to 30 nm, and they retain hexagonal symmetry.Isotopic exchange appears to be the sum of surface exchange and interior exchange. At 1100-1400 °C, interior exchange exceeded surface exchange, probably by a combination of grain growth, as determined by increase in crystallite size, recrystallization, as observed in FESEM images, and diffusion. In some runs at 1200 and 1400 °C with an isotopic contrast between the initial graphite and calcite of close to 50‰, equilibrium fractionation was actually overstepped due to a kinetic effect. A weighted regression of fractionation factors from the high-temperature runs yields the line of equilibrium interior exchange:

     

Cavity expansion in cross‐anisotropic rock

Schistous rock can be considered—in a first approximation—as cross‐anisotropic linear elastic material. The determination of the corresponding material constants on the basis of the laboratory investigation of rock samples often fails, as the extraction of appropriate cores proves to be unfeasible (the cores disintegrate if the schistosity is pronounced). In this paper a new method is presented to determine the material constants of a linear elastic cross‐anisotropic rock on the basis of cavity expansion field tests, e.g. with a radial jack. To this purpose, an analytic approximation for the deformation of a hydrostatically loaded cylindrical cavity in cross‐anisotropic rock is derived which serves to the inverse analysis of the material parameters. Copyright © 2010 John Wiley & Sons, Ltd.     

Oxygen and hydrogen isotope fractionation in serpentine-water and talc-water systems from 250 to 450 °C, 50 MPa

Oxygen and hydrogen isotope fractionation factors in the talc-water and serpentine-water systems have been determined by laboratory experiment from 250 to 450 °C at 50 MPa using the partial exchange technique. Talc was synthesized from brucite + quartz, resulting in nearly 100% exchange during reaction at 350 and 450 °C. For serpentine, D-H exchange was much more rapid than ¹⁸O-¹⁶O exchange when natural chrysotile fibers were employed in the initial charge. In experiments with lizardite as the starting charge, recrystallization to chrysotile enhanced the rate of ¹⁸O-¹⁶O exchange with the coexisting aqueous phase. Oxygen isotope fractionation factors in both the talc-water and serpentine-water systems decrease with increasing temperature and can be described from 250 to 450 °C by the relationships: 1000 ln  = 11.70 × 10⁶/T² − 25.49 × 10³/T + 12.48 and 1000 ln  = 3.49 × 10⁶/T² − 9.48 where T is temperature in Kelvin. Over the same temperature interval at 50 MPa, talc-water D-H fractionation is only weakly dependent on temperature, similar to brucite and chlorite, and can be described by the equation: 1000 ln = 10.88 × 10⁶/T² − 41.52 × 10³/T + 5.61 where T is temperature in Kelvin. Our D-H serpentine-water fractionation factors calibrated by experiment decrease with temperature and form a consistent trend with fractionation factors derived from lower temperature field calibrations. By regression of these data, we have refined and extended the D-H fractionation curve from 25 to 450 °C, 50 MPa as follows: 1000 ln  = 3.436 × 10⁶/T² − 34.736 × 10³/T + 21.67 where T is temperature in Kelvin. These new data should improve the application of D-H and ¹⁸O-¹⁶O isotopes to constrain the temperature and origin of hydrothermal fluids responsible for serpentine formation in a variety of geologic settings.     

Estimation and testing of higher-order spatial autoregressive panel data error component models

This paper develops an estimator for higher-order spatial autoregressive panel data error component models with spatial autoregressive disturbances, SARAR(R,S). We derive the moment conditions and optimal weighting matrix without distributional assumptions for a generalized moments (GM) estimation procedure of the spatial autoregressive parameters of the disturbance process and define a generalized two-stage least squares estimator for the regression parameters of the model. We prove consistency of the proposed estimators, derive their joint asymptotic distribution, and provide Monte Carlo evidence on their small sample performance.     

Where Am I? Investigating Map Matching During Self‐Localization With Mobile Eye Tracking in an Urban Environment

Self‐localization is the process of identifying one's current position on a map, and it is a crucial part of any wayfinding process. During self‐localization the wayfinder matches visually perceptible features of the environment, such as landmarks, with map symbols to constrain potential locations on the map. The success of this visual matching process constitutes an important factor for the success of self‐localization. In this research we aim at observing the visual matching process between environment and map during self‐localization with real‐world mobile eye tracking. We report on one orientation and one self‐localization experiment, both in an outdoor urban environment. The gaze data collected during the experiments show that successful participants put significantly more visual attention to those symbols on the map that were helpful in the given situation than unsuccessful participants. A sequence analysis revealed that they also had significantly more switches of visual attention between map symbols and their corresponding landmarks in the environment, which suggests they were following a more effective self‐localization strategy.     

How to compare movement? A review of physical movement similarity measures in geographic information science and beyond

In geographic information science, a plethora of different approaches and methods is used to assess the similarity of movement. Some of these approaches term two moving objects similar if they share akin paths. Others require objects to move at similar speed and yet others consider movement similar if it occurs at the same time. We believe that a structured and comprehensive classification of movement comparison measures is missing. We argue that such a classification not only depicts the status quo of qualitative and quantitative movement analysis, but also allows for identifying those aspects of movement for which similarity measures are scarce or entirely missing.

In this review paper we, first, decompose movement into its spatial, temporal, and spatiotemporal movement parameters. A movement parameter is a physical quantity of movement, such as speed, spatial path, or temporal duration. For each of these parameters we then review qualitative and quantitative methods of how to compare movement. Thus, we provide a systematic and comprehensive classification of different movement similarity measures used in geographic information science. This classification is a valuable first step toward a GIS toolbox comprising all relevant movement comparison methods.     

0.99999999 confidence ambiguity resolution with GPS and Galileo

In this short contribution it is demonstrated how integer carrier phase cycle ambiguity resolution will perform in near future, when the US GPS gets modernized and the European Galileo becomes operational. The capability of ambiguity resolution is analyzed in the context of precise differential positioning over short, medium and long distances. Starting from dual-frequency operation with GPS at present, particularly augmenting the number of satellites turns out to have beneficial consequences on the capability of correctly resolving the ambiguities. With a 'double' constellation, on short baselines, the confidence of the integer ambiguity solution increases to a level of 0.99999999 or beyond. Electronic Publication