Drop size dependent sulfate distribution in a growing cloud     

G. J. H. Roelofs 《Journal of Atmospheric Chemistry》1992,14(1-4):109-118

A simple entraining air parcel model including cloud microphysical and chemical processes is used to calculate the distribution of sulfate over the drop sizes under continental background conditions. Under these conditions the aerosol sulfate is predicted to contribute the largest amount of aqueous sulfate in cloud drops. The sulfate produced by oxidation is found to contribute significantly in drops larger than 10 m radius.  相似文献   

Measurements of peroxyacetylnitrate in the marine boundary layer over the Atlantic     

K. P. Müller  J. Rudolph 《Journal of Atmospheric Chemistry》1992,15(3-4):361-367

The atmospheric concentration of peroxyacetylnitrate (PAN) was measured during a cruise of the R.S. Polarstern from Bremerhaven (Germany) to Rio Grande do Sul (Brazil) in September/ October 1988. The measurements were made in-situ by a combination of electron capture gaschromatography with a cryogenic preconcentration step. The theoretical lower limit of detection (3) was 0.4 ppt. The mixing ratios of PAN varied by more than three orders of magnitude from 2000 ppt in the English Channel to less than 0.4 ppt south of the Azores (38° N). South of 35° N, PAN levels were below the detection limit, except at 30–31° S off the eastern coast of South America. Here, PAN mixing ratios of 10 to 100 ppt were detected in continentally influenced air masses. Detectable levels of PAN were mostly observed in air masses of continental or high northern origin. Changes in the wind directions were usually associated with substantial changes in the PAN mixing ratios.  相似文献   

Theory of the local scale parameter method for EDM     

F. K. Brunner  J. M. Rüeger 《Journal of Geodesy》1992,66(4):355-364

The determination of a representative refractive index for the wave path is the main limitation of the attainable accuracy in electronic distance measurement. To overcome this limitation the length ratio method was initially proposed and later developed into the local scale parameter (LSP) method. In this paper, the mathematical model of the LSP method is derived for electro-optical distance measurement from first principles based on the physics of the atmospheric boundary layer. The model does not rely on standard atmospheres. It is shown that atmospheric temperatures and pressures must be observed at instrument stations but not at reflector stations. Appropriate LSP field procedures and the results of some field experiments are summarized. The method consistently produces accuracies of better than ±1 ppm. Use of the method is recommended for high precision (trilateration) networks, which need to be measured repeatedly and where absolute scale is not relevant.  相似文献   

Diploptene: an indicator of terrigenous organic carbon in Washington coastal sediments   总被引：1，自引：0，他引：1  

Prahl FG  Hayes JM  Xie T-M 《Limnology and oceanography》1992,37(6):1290-1300

The pentacyclic triterpene 17 beta(H),21 beta(H)-hop-22(29)-ene (diploptene) occurs in sediments throughout the Columbia River drainage basin and off the southern coast of Washington state in concentrations comparable to long-chain plantwax n-alkanes. The same relationship is evident for diploptene and long-chain n-alkanes in soils from the Willamette Valley. Microorganisms indigenous to soils and soil erosion are indicated as the biological source and physical process, respectively, for diploptene in coastal sediments. Similarity between the stable carbon isotopic composition (delta 13CPDB) of diploptene isolated from soil in the Willamette Valley (-31.2 +/- 0.3%) and from sediments deposited throughout the Washington coastal environment (-31.2 +/- 0.5%) supports this argument. Values of delta for diploptene in river sediments are variable and 8-17% lighter, indicating that an additional biological source such as methane-oxidizing bacteria makes a significant contribution to the diploptene record in river sediments. Selective biodegradation resulting from a difference in the physicochemical association within eroded particles can explain the absence of the more-13C-depleted form of diploptene in Washington coastal sediments, but this mechanism remains unproven.  相似文献   

Atmospheric water vapor flux,bifurcation of the thermohaline circulation,and climate change     

Huaxiao Wang  G Edward Birchfield 《Climate Dynamics》1992,8(1):49-53

Latitudinal heat transport in the ocean and atmosphere represents a fundamental process of the Earth's climate system. The ocean component of heat transport is effected by the thermohaline circulation. Changes in this circulation, and hence latitudinal heat transport, would have a significant effect on global climate. Paleoclimate evidence from the Greenland ice cores and deep sea sediment cores suggests that during much of glacial time the climate system oscillated between two different states. Bimodal equilibrium states of the thermohaline circulation have been demonstrated in climate models. We address the question of the role of the atmospheric hydrological cycle on the global thermohaline circulation and the feedback to the climate system through changes in the ocean's latitudinal heat transport, with a simple coupled ocean-atmosphere energy-salt balance model. Two components of the atmospheric hydrological cycle, i.e., latitudinal water vapor transport and the net flux of water vapor from the Atlantic to the Pacific Ocean appear to play separate roles. If the inter-basin transport is sufficiently large, small changes in water vapor transport over the North Atlantic can effect bifurcation or a rapid transition between two different equilibria in the global thermohaline circulation; maximum difference between the modes occurs in the North Atlantic. If the inter-basin transport is from the Pacific to the Atlantic and sufficiently large, latitudinal vapor transport in the North Pacific controls the bifurcations, with maximum changes occurring in the North Pacific. For intermediate values of inter-basin transport, no rapid transitions occur in either basin. In the regime with vapor flux from the Atlantic to the Pacific, the on mode has strong production of deep water in the North Atlantic and a large flux of heat to the atmosphere from the high latitude North Atlantic. The off mode has strong deep water production in the Southern Ocean and weak production in the North Pacific. Heat transport into the high latitude North Atlantic by the ocean is reduced to about 20% of the on mode value. For estimated values of water vapor transport for the present climate the model asserts that while water vapor transport from the Atlantic to the Pacific Ocean is sufficiently large to make the North Atlantic the dominant region for deep water production, latitudinal water vapor transport is sufficiently low that the thermohaline circulation appears stable, i.e., far from a bifurcation point. This conclusion is supported to some extent by the fact that the high latitude temperature of the atmosphere as recorded in the Greenland ice cores has changed little over the last 9000 years.  相似文献   

Petrology of ultramafic and mafic xenoliths in picrite of Kahoolawe Island,Hawaii     

E A Rudek  R V Fodor  G R Bauer 《Bulletin of Volcanology》1992,55(1-2):74-84

A picrite lava (22 wt% MgO; 35 vol.% ol) along the western shore of the1.3–1.4 Ma Kahoolawe tholeiitic shield, Hawaii, contains small xenoliths of harzburgite, lherzolite, norite, and wehrlite. The various rock types have textures where either orthopyroxene, clinopyroxene, or plagioclase is in a poikilitic relationship with olivine. The Mg#s of the olivine, orthopyroxene, and clinopyroxene in this xenolith suite range between 86 and 82; spinel Mg#s range from 60 to 49, and plagioclase is An_75–80. A ⁸⁷Sr/⁸⁶Sr ratio for one ol-norite xenolith is 0.70444. In comparison, the host picrite has olivine phenocrysts with an average Mg# of 86.2 (range 87.5–84.5), and a whole-rock ⁸⁷Sr/⁸⁶Sr ratio of 0.70426. Textural and isotopic information together with mineral compositions indicate that the xenoliths are related to Kahoolawe tholeiitic magmatism, but are not crystallization products of the magma represented by their host picrite. Rather, the xenoliths are crystalline products of earlier primitive liquids (FeO/MgO ranging 1 to 1.3) at 5–9 kbar in the cumulate environment of a magma reservoir or conduit system. The presence of ultramafic xenoliths in picrite but not in typical Kahoolawe tholeiitic lava (6–9 wt% MgO) is consistent with replenishment of reservoirs by dense Mg-rich magma emplaced beneath resident, less dense tholeiitic magma. Mg-rich magmas have proximity to reservoir cumulate zones and are therefore more likely than fractionated residual liquids to entrain fragments of cumulate rock.  相似文献   

Nd-, Sr-, O-isotopic and chemical evidence for a two-stage contamination history of mantle magma in the Central-Alpine Bergell intrusion     

Friedhelm von Blanckenburg  Gretchen Früh-Green  Karlheinz Diethelm  Peter Stille 《Contributions to Mineralogy and Petrology》1992,110(1):33-45

Two different contamination processes have been identified as having been operative in the genesis of a plutonic suite: initial contamination of a mantle source, and subsequent crustal contamination of uprising partial melts from the mantle. These processes are indicated by a detailed analyses of Nd, Sr, and oxygen isotopes together with major-and trace-elements of the 32–30 Ma calc-alkaline Bergell intrusion. This intrusion is located at the suture of the Alpine continental collision zone and contains rock types capable of discriminating between mantle and intracrustal processes. A range from basaltic-andesitic dykes in the surrounding country rocks, cumulitic hornblendites, gabbros, tonalite, granodiorite and lamprophyres, to pegmatites and aplites, is exposed in this single intrusion. The results of REE modelling and isotopic compositions of the basic members suggest that the cumulates were fractionated from a picrobasaltic liquid originating by partial melting of enriched subcontinental mantle (_Nd=+4). Increases in ⁸⁷Sr/⁸⁶Sr (0.7055) and ¹⁸O(+6.7) in these samples relative to the mantle array and compositions of other Periadriatic intrusions are most likely the result of an initial contamination of the mantle source by dehydration or partial melting of altered subducted oceanic crust. Slight differentiation of such a picrobasaltic liquid produced the basaltic-andesitic dykes. Simultaneous fractional crystallization and contamination of the uprising magma by continental crust produced crustal isotopic signatures which increase with acidity to values of (_Nd=-7.6), ⁸⁷Sr/⁸⁶Sr=0.716 and ¹⁸O=+10. The crustal imprint and LREE enrichment in the dominating tonalite increase with decreasing crystallization depth which indicates that the tonalites were emplaced in several distinct batches with different degrees of contamination. Shoshonitic lamprophyres, which intruded into the partly solidified granodiorite, were generated in a deep, strongly contaminated mantle source. The posttectonic 26 Ma Novate leucogranite is not cogenetic with the main Bergell body, but rather formed from a predominantly crustal source. If the described features are indeed due to mantle source contamination processes, which are well known for volcanic arcs, it must be concluded that these may also play a significant role in the genesis of calcalkaline plutonic suites.  相似文献   

Fractional Crystallization and Liquid Immiscibility Processes in the Alkaline-Carbonatite Complex of Juqui (So Paulo, Brazil)     

BECCALUVA  L.; BARBIERI  M.; BORN  H.; BROTZU  P.; COLTORTI  M.; CONTE  A.; GARBARINO  C.; G.  C.B. GOMES; M.  ACCIOTTA; MORBIDELLI  L.; RUBERTI  E.; SIENA  F.; TRAVERSA  G. 《Journal of Petrology》1992,33(6):1371-1404

The Juqui circular intrusion, which is Cretaceous in age (130–135Ma), crops out in the Precambrian gneissic basement in Brazilover an area of 14 km2. It consists of olivine clinopyroxen-itecumulates (with minor olivine gabbros) in the northeastern sector(74 vol.%), whereas ijolites-melteigites-urtites (4%) and nephelinesyenites with minor essexites and syenodiorites (21%) outlinesubannular concentric patterns with an Mg-carbonatite core (1%), in the southwestern part of the complex. Petrographical, bulk rock, and mineral compositional trendsindicate that the origin of the complex can be largely accountedfor by shallow-level fractional crystallization of a carbonatedbasanitic parental magma. Such a magma was generated deep inthe subcontinental lithosphere by low-degree partial meltingof a garnet-phlogopite peridotite source. Mass-balance calculations in agreement with field volume estimatespermit definition of several fractionation stages of the magmaticevolution under nearly closed-system conditions, with inwarddevelopment of zonally arranged side-wall cumulates. These stagesinvolved: (1) fractionation from basanite to essexite magma(liquid fraction F = 33–5%) by crystallization of olivineclinopyroxenite plus minor olivine alkali gabbro cumulates;(2) derivation of the least differentiated mafic nepheline syenite(F = 5–5 %) from essexitic magma by subtraction of a syenodioriteassemblage; (3) exsolution of a carbonatite liquid (5%) froma CO₂-enriched mafic nepheline syenite magma, which also underwentcontinuous fractionation giving rise to ijolite-melteigite-urtitecumulates. The proportion of cumulus clinopyroxene and biotiteand intercumulus nepheline and alkali feldspar in these lastrocks, as well as the absence of alkalis in carbonatite, maybe attributed, at least in part, to loss of alkali-rich hydrousfluids released during and after the unmixing formation of thetwo conjugate liquids. The KD values determined for Mg-carbonatite/nepheline syeniteare lower (1–4–2–9) for light rare earth elements(LREE) than for REE from Eu to Yb (4–6–7–8),in contrast to recent experimental results (Hamilton et al.,1989). A possible explanation is that Juquia Mg-carbonatiterepresents an alreadydifferentiated magma, which underwent extensivefractionation of LREE-enriched calcite. In this way, the highvariability of K₀ REE patterns observed in several alkaline-carbonatitecomplexes can also be accounted for. The remarkably constant initial ⁸⁷Sr/⁸⁶Sr ratios (mostly between0–7052 and 0–7057) support the interpretation ofthe intrusion as having been generated by fractrional crystallizationand liquid immiscibility from a common parental magma. Iligherisotopic ratios (0–7060–0–7078), found mainlyin dykes and in the border facies of the intrusion, may be dueto contamination by the gecissic basement.  相似文献   

Geological,fluid inclusion and stable isotope studies of Mo mineralization,Galway Granite,Ireland     

V. Gallagher  M. Feely  H. Högelsberger  G. R. T. Jenkin  A. E. Fallick 《Mineralium Deposita》1992,27(4):314-325

Mo mineralization within the Galway Granite at Mace Head and Murvey, Connemara, western Ireland, has many features of classic porphyry Mo deposits including a chemically evolved I-type granite host, associated K- and Si-rich alteration, quartz vein(Mace Head) and granite-hosted (Murvey) molybdenite, chalcopyrite, pyrite and magnetite mineralization and a gangue assemblage which includes quartz, muscovite and K-feldspar. Most fluid inclusions in quartz veins homogenize in the range 100–350°C and have a salinity of 1–13 eq. wt.% NaCl. They display Th-salinity covariation consistent with a hypothesis of dilution of magmatic water by influx of meteoric water. CO₂-bearing inclusions in an intensely mineralized vein at Mace Head provide an estimated minimum trapping temperature and pressure for the mineralizing fluid of 355°C and 1.2 kb and are interpreted to represent a H₂O-CO₂ fluid, weakly enriched in Mo, produced in a magma chamber by decompression-activated unmixing from a dense Mo-bearing NaCl-H₂O-CO₂ fluid. ³⁴S values of most sulphides range from c. 0 at Murvey to 3–4 at Mace Head and are consistent with a magmatic origin. Most quartz vein samples have ¹⁸O of 9–10.3 and were precipitated from a hydrothermal fluid with ¹⁸O of 4.6–6.7. Some have ¹⁸O of 6–7 and reflect introduction of meteoric water along vein margins. Quartz-muscovite oxygen isotope geothermometry combined with fluid inclusion data indicate precipitation of mineralized veins in the temperature range 360–450°C and between 1 and 2 kb. Whole rock granite samples display a clear ¹⁸O-D trend towards the composition of Connemara meteoric waters. The mineralization is interpreted as having been produced by highlyfractionated granite magma; meteoric water interaction postdates the main mineralizing event. The differences between the Mace Head and Murvey mineralizations reflect trapping of migrating mineralizing fluid in structural traps at Mace Head and precipitation of mineralization in the granite itself at Murvey.  相似文献   

The energetics of interaction between oxygen vacancies in sillimanite: A model for the mullite structure     

S. Padlewski  V. Heine  G. D. Price 《Physics and Chemistry of Minerals》1992,19(3):196-202

A microscopic model is introduced to discuss the modulated structure of mullite. The oxygen vacancies of this aluminosilicate are known to play a central role. In particular, a single vacancy strongly orders its surrounding Al/Si tetrahedral sites. It is shown in this work that if two oxygen vacancies approach too closely to one another, their Al/Si dressing overlap. This situation results in repulsive interaction. The field of interaction between the vacancies is estimated with the use of an atomistic computer simulation. We use a Bragg-Williams type of theory to dicuss the ordering pattern of the vacancies. Due to frustration between the two dominant repulsive interactions, our model predicts a modulated phase transition in agreement with observation.  相似文献