A verification of some methods to determine the fluxes of momentum,sensible heat,and water vapour using standard deviation and structure parameter of scalar meteorological quantities

A set of micro-meteorological data collected over a horizontal, uniform terrain (the plain of La Crau, France) in June 1987 is analysed. Conditions were predominantly sunny and arid, while due to the Mistral the wind speed could exceed 10 m/s. Verification of several methods to evaluate surface fluxes of heat, momentum and water vapour from the standard deviation of temperature, wind and specific humidity is presented. Also, a similar approach using the structure parameter of temperature is considered. These methods are all based on Monin-Obukhov (M-O) similarity theory. It is found that the standard deviation of temperature, vertical and horizontal wind speed as well as the structure parameter for temperature behave according to M-O similarity. It is shown that the sensible heat flux and friction velocity can be determined from a fast response thermometer and a cup anemometer. Also, it appears that the analytic solution of the set of governing equations as derived by the first author yields good results. M-O theory does not appear to work for the standard deviation of specific humidity. This may be due to the relative importance of large eddies.     

Arctic haze: Perturbation to the radiation field

Summary A model of the polluted arctic troposphere is constructed to estimate the magnitude and seasonal variation of the climate forcing function of arctic haze. Using a pill-box bathtub model for the Arctic and envisioning it to be filled with pollution from industrial sources in Eurasia, we estimate that maximum climate perturbation from arctic contamination occurs in the spring months. The major perturbation to the radiation budget is a lowering of the albedo (heating) of the earth-atmosphere system around the vernal equinox and is due to a trace amount (about 5% by mass) of black carbon associated with the removal-resistant submicron mode of aerosols. The black carbon over the reflecting polar ice/snow introduces a heating of about 1.5 degree per day into the haze layer.With 8 Figures     

The concentration and isotopic composition of carbon in basaltic glasses from the Juan de Fuca Ridge, Pacific Ocean

The abundance and 13C/12C ratios of carbon were analyzed in basaltic glass from twenty locations along the Juan de Fuca Ridge using a 3-step combustion/extraction technique. Carbon released during the first two combustion steps at 400-500 degrees C and 600-650 degrees C is interpreted to be secondary, and only the carbon recovered during a final combustion step at approximately 1200 degrees C is thought to be indigenous to the samples. For carbon released at approximately 1200 degrees C, glasses analyzed as 1-2 mm chips contained 23-146 ppm C with delta 13C values of -4.8 to -9.3%, whereas samples crushed to 38-63 microns or 63-90 microns yielded 56-103 ppm C with delta 13C values of -6.1 to -9.2%. The concentrations and isotopic compositions of the primary carbon dissolved in the glasses and present in the vesicles are similar to those previously reported for other ocean-ridge basalts. The Juan de Fuca basaltic magmas were not in equilibrium with respect to carbon when they erupted and quenched on the sea floor. Evidence of disequilibrium includes (1) a large range of carbon contents among glasses collected at similar depths, (2) a highly variable calculated carbon isotopic fractionation between melt and vapor determined by comparing crushed and uncrushed splits of the same sample, and (3) a lack of correlation between vesicle abundance, carbon concentration, and depth of eruption. Variations in carbon concentration and delta 13C ratios along the ridge do not correlate with major element chemistry. The observed relationship between carbon concentrations and delta 13C values may be explained by late-stage, variable degrees of open-system (Rayleigh-like) degassing.     

Kinetics of peptide hydrolysis and amino acid decomposition at high temperature

Dipeptide hydrolysis and amino acid decomposition appear to follow a first-order rate law. The hydrolysis rate increases exponentially with increasing temperature in aqueous solution at both 265 atm and water steam pressures over the temperature range of 100 to 220 degrees C. Dipeptide hydrolysis has a lower apparent activation energy at 265 atm (44.1 KJ/mol) than at water steam pressure (98.9 KJ/mol). At lower temperatures (<200-220 degrees C), the rate of peptide bond hydrolysis is faster at 265 atm than at water steam pressure. At higher temperatures (>200-220 degrees C), however, peptide bond hydrolysis is slower at 265 atm than at water steam pressure. In aqueous solution, amino acid decomposition rates also increase exponentially with increasing temperature. Amino acid decomposition rates are much higher at 265 atm than at water steam pressure over the entire temperature range investigated.     

Chemically Distinct Mafic Dike/Sill Sequences of Contrasting Age Ranges, Sawyers Bar Area, Central Klamath Mountains, Northern California

Mafic hypabyssal rocks in the western Triassic and Paleozoicbelt provide important clues to the nature of accretion andarc evolution along this sector of the North American margin.In the east-central part of the belt, near Sawyers Bar, somediabases have been metamorphosed before and accompanying emplacementof the mid-Jurassic English Peak and Russian Peak granitoidswithin the North Fork/Salmon River + Stuart Fork amalgamatedterrane. Certain other dikes/sills, chiefly mafic microdiorites,cut the calc-alkaline plutons but are themselves deutericallyaltered; at least two of these mafic microdiorites near theEnglish Peak body possess hornfelsic textures. Thus, althoughmost mafic microdioritic hypabyssals seem to have been injectedafter granitoid emplacement, a few must have preceded plutonicintrusion. Macroscopic appearances, phase assemblages, mineralcompositions, and textures of the mafic microdioritic and metadiabasicdikes/sills are sufficiently alike to preclude the ready fieldand petrographic distinction of the different magma series.Bulk-rock chemistries fall into two groups, however, with slightlymore porphyritic, altered, synplutonic mafic microdiorite samplesbeing distinctly richer in Si, K, P, Rb, Sr, Zr, and light rareearth elements (LREE) relative to the Mg + Cr + Ni-rich, preplutonicmetadiabases. Analyzed mafic microdiorites have bulk-rock chemicaland isotopic compositions similar to the more ferromagnesianportions of the mid-Jurassic English Peak and Russian Peak plutoniccomplexes, whereas the metadiabases are comparable with theearly Mesozoic Salmon River metabasalts. Although the two groupsof dikes/sills probably overlap in age of emplacement, the maficmicrodiorite group is predominantly younger and uniform in oxygenisotopic composition (bulk-rock ¹⁸O 11•37, 11•4 and11•46) compared with the older, more intensely metamorphosed,and variably metasomatized Salmon River metadiabases (bulk-rock5¹⁸ 9•4, 11•0, and 15•3). Both types of maficdike/sill locally intrude the more easterly Stuart Fork terrane.Therefore, suturing and regional metamorphism of the outboardNorth Fork/Salmon River oceanic-island arc and inboard StuartFork subduction complex must have occurred during terminal stagesof injection of the pregranitoid diabases into the North Fork(oceanic-island basalts)/Salmon River (island-arc tholeiites)arc + Stuart Fork terrane, but before invasion of the amalgamatedterrane assembly by the calc-alkaline plutons and most compositionallyrelated synplutonic mafic microdiorite dikes/sills. Becauseof their lateral continuation both north and south of the SawyersBar area, the North Fork/Salmon River igneous suite documentsthe construction of an oceanic arc of considerable lateral extentin the central Klamaths before terrane accretion. Suturing wasimmediately followed by the mid-Jurassic intrusion of calc-alkalineplutons + syngranitoid mafic microdioritic hypabyssals.     

Stratiform and vein U,Mo and Cu mineralization in the Novoveská Huta area,CSFR

U-Mo and Cu mineralization occurs in horizons as well as in veins in the Permian formations near Novoveská Huta. Ore mineralization is represented by uraninite, U-Ti oxides, coffinite, molybdenite, chalcopyrite, tennantite and pyrite. The isotopic composition of S and C displays a larger variability in the stratiform ores (³⁴S from –32.7 to +2.7 and ¹³C from –27.1 to — 0.5) These data suggest mixing of meteoric solutions with fluids of volcanic origin and a complex history. There is a narrower range of ³⁴S from –18.8 to –4.6 and ¹³C from –6.3 to –2.5% in quartz-carbonate veins with Cu mineralization suggesting a deep source of ore-bearing solutions. The Permian volcanics were a significant source of ore elements.Their contents of U, Mo, Cu and Y are from two to eight times higher than in sedimentary rocks. Accumulations of ore elements in the horizons were formed by the reduction and adsorption processes 240 ± 30 Ma ago according to U-Pb isotopic dating. Due to Alpine tectonism, these low-grade ores (U<0.1 wt%) were remobilized and higher-grade U-Mo ores (U>0.1 wt%) were formed 130 ± 20 Ma ago at temperatures ranging from 110 to 120° C, according to fluid inclusions. Younger veins with Cu mineralization were formed 115 ± 10 Ma according to the model age of Pb at temperatures ranging from 95 to 190°C.     

Cu 2p absorption spectroscopy as a probe for the site occupancy of (ZnxCu1−x)WO4 solid solution

The solid solution sanmartinite (ZnWO₄)—cuproscheelite (CuWO₄) has been studied using Cu 2p X-ray absorption spectroscopy. While a single L₃ absorption peak is observed for CuWO₄, two distinct L₃ absorption peaks with a separation of ～0.8 eV are observed for the intermediate samples in the solid solution. The two peaks represent distinct Cu sites: one with all CuO₆ next nearest neighbours in the (Cu,Zn)O₆ chains, another having at least one ZnO₆ next nearest neighbour. Both sites show a linear increase in covalency as a function of increasing Cu-content. The relative intensities of the two absorption peaks is dependent upon the Cu-content and has been used to model the site occupancies. The results reveal that the local structural effects can be associated with a composition-dependent structural phase transition from P2/c (ZnWO₄) to P $\bar 1$ (CuWO₄). Deviations from a single-site model are explained in terms of the local environments, and evidence for site preferences and local clustering are explored.     

Effects of onshore and offshore topography on sea breeze circulation: An observational study at eastern Attica,Greece

Field measurements of wind, air temperature and humidity were taken at the eastern part of the Attika district in June 1991, to examine the topographic influences exerted on the local sea breezes. These influences are due either to the elongated Evia island, faced by the northern half of Attica coastline some tens of kilometers offshore, or to the coast-parallel range of Hymettos mountain, rising steeply 12 km onshore. The instrumentation consisted mainly of three tethered meteorological balloons released at characteristic sires (i.e., the coast, a location between shoreline and mountain foot and the mountain top) and three autographic ground-based anemometers operating at selected locations. Data from the ground-based and upper air stations of the Hellenic National Meteorological Service, as well as the diurnal weather maps were also obtained and analyzed. Observations were made under different synoptic wind and the latter was found to determine remarkably the significance of the topographic effects. A preliminary two-dimensional numerical approach was also made concerning the sea breeze capability to reach the Hymettos mountain top in the case of a weak opposing geostrophic flow.     

Automatic equipment to monitor groundwater radon

Prototype instrumentation, able to automatically measure groundwater radon content variations, is presented. The equipment is made of stainless steel and has spherical valves with automatic and pneumatic control. The deemanation of the gases from the water is obtained by evacuating a suitable expansion chamber. The instrumentation can make discrete sampling ranging from 1 per hour to 1 per 99 hours. The equipment was tested in the laboratory: the efficiency was measured by means of a²⁶⁶Ra solution. A mean value of (0.65±0.07) count/s/Bq was obtained. A calibration test was carried out by comparing countings from the automatic equipment with those obtained by the standard laboratory cell. Results of an operational check over a period of approximately one year indicate that variations in radon at the calibration site are attributable more to meteorological than to tectonic causes.     

Crystal-chemistry of clinopyroxene from Sunda volcanic arc

Summary The crystal-chemistry of clinopyroxene from a suite of Sunda arc volcanic rocks was investigated by X-ray structure refinement and microprobe analysis. Relationships with clinopyroxene from volcanic rocks of the intraplate environment were highlighted.Sunda clinopyroxenes were distinguished into two groups. The first consists of clinopyroxene from SiO₂-saturated rock types and crystal rim from SiO₂-undersaturated rock types, the second of crystal core from SiO₂-undersaturated rock types. The crystal chemical behaviour of the two groups differs significantly, mainly in the geometrical relationships between M2 and T sites. While in the first group M2-O3 and T-O3 bond lengths shorten and lengthen respectively due to Ca and Al^IV increase, in the second group in which M2 site is almost fully coordinated by Ca, -O3 bond lengths are forced to lengthen in spite of low Al^IV content, in order to mantain the local charge balance around the O3 oxygens.It is noteworthy that Sunda clinopyroxene shows strong analogies with that from basaltic rocks from the Ethiopian plateau and K-rich lavas from the Roman Province respectively, reflecting similarities between the composition and mineralogical assemblages of the host rocks, although they all came from different tectonic environments. A relationship between intracrystalline Mg-Fe 2+ disorder and the explosive character of the volcanism is demonstrated.

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Kristallchemie von Klinopyroxenen aus Gesteinen des Vulkanbogens der Sunda-Inseln

Zusammenfassung Die Kristallchemie von Klinopyroxenen aus einer Serie von vulkanischen Gesteinen des Sunda-Bogens wurde mit Röntgen-Strukturverfeinerungen und Mikrosonden-analysen untersucht. Beziehungen zu Klinopyroxenen vulkanischer Gesteine aus intra-Plattenpositionen werden beleuchtet. Die Sunda-Klinopyroxene wurden in zwei Gruppen eingeteilt. Die erste umfaßt Klinopyroxene SiO₂-gesättigter Gesteinstypen und Kristallsäume SiO₂-untersättigter Gesteinstypen, die zweite Kristallkerne SiO₂-untersättigter Gesteinstypen. Das kristallchemische Verhalten der beiden Gruppen unterscheidet sich beträchtlich, hauptsächlich in den geometrischen Beziehungen zwischen den M2 und T Positionen. Während in der ersten Gruppe die M2-O3 und T-O3 Bindungsldngen durch Zunahme von Ca und Al^IV kleiner bzw. größer werden, sind in der zweiten Gruppe die T-O3 Bindungslängen trotz niedrigen Al^IV Gehaltes zu einer Vergrößerung gezwungen, damit um die O3 Atome der lokale Ladungsausgleich erhalten bleibt.Es ist bemerkenswert, daß die Sunda-Klinopyroxene große Analogien zu denen aus basaltischen Gesteinen des Abessinischen Plateaus und aus K-reichen Laven sowohl der Römischen Provinz als auch des Westafrikanischen Grabens zeigen. Dies spiegelt Ähnlichkeiten zwischen Zusammensetzung und Mineralbestand der Muttergesteine wider, obwohl sie all aus tektonisch unterschiedlichen Positionen kommen.Eine Beziehung zwischen intrakristalliner Mg-Fe²⁺ Unordnung und dem explosiven Charakter des Vulkanismus wird aufgezeigt.