Derivation of A-type Granites from a Dehydrated Charnockitic Lower Crust: Evidence from the Chaelundi Complex, Eastern Australia

Triassic I- and A-type granites of the Chaelundi Complex, NewEngland Fold Belt, eastern Australia, were generated in a subduction-relatedtectonic setting. Although isotopic ages of the suites are indistinguishable,field relations indicate that the A-type is younger. The mostmafic granitoids from each suite have similar silica contents(66–68% SiO₂), slightly LREE enriched patterns withoutEu anomalies, low Rb/Sr and K/Ba ratios, and high K/Rb ratios,suggesting that both represent parental magmas. The A-type isdistinguished mineralogically by abundant orthoclase and sodicplagioclase (total >60%), ferro-hornblende, annite and allanite.In contrast, the I-type has more hornblende and biotite, whichare more magnesian in composition, and less feldspar. The parentalmagmas of both suites have many similar geochemical characteristics,although the A-type has slightly higher alkalis, Zr, Hf, Znand LREE, and lower CaO, MgO, Sr, V, Cr, Ni and Fe³⁺/Fe. Thegeochemical properties characteristic of leucocratic A-typegranites, such as high Ga/Al, Nb, , HREE and F contents, areonly manifest in the more felsic members of the A-type suite.These features were produced by 70% fractional crystallizationof feldspar, hornblende, quartz and biotite. Both granite suites were generated by water-undersaturated partialmelting of a similar source, but the A-type parent magma resultedfrom lower aH₂O conditions during partial melting. Generationand rapid ascent of the earlier 1-type magma during disequilibriumpartial melting produced a relatively anhydrous, but not refractory,charnockitic lower crust. Continued thermal input from mantle-derivedmagmas, during continuing subduction, partially melted the ‘charnockitized’lower crust at temperatures in excess of 900C, to produce A-typemagmas. Charnockitic magmas (C-type) form in a similar way toA-type magmas, although their different composition reflectsvariations in the anhydrous lower-crustal mineral assemblagesthat remain after the previous (1-type) granite-forming event. The New England Fold Belt was a subduction—accretion complexuntil the late Carboniferous, when the deeper parts underwentpartial melting to produce S-type granites. As the I-and A-typegranites intruded penecontemporaneously, a tonalitic sourcemodel for genesis of the Chaelundi A-type is untenable. KEY WORDS: A-type; charnockitization; eastern Australia ^*Corresponding author.     

Non-ideal Mg-Fe binary mixing in cordierite: Constraints from experimental data on Mg-Fe partitioning in garnet and cordierite and a reformulation of garnet-cordierite geothermometer

The non-ideal regular Mg-Fe binary in cordierite has been derived through multivariate linear regression of the expressionRT InK_D +(P- 1)ΔVK ₁ ⁰ , 298 along with updated subfegular mixing parameter of almandine-pyrope solution (Hackler and Wood 1989; Berman 1990). The data base used for multivariate analyses consists of published experimental data (n = 177) on Mg-Fe partitioning between garnet and cordierite in theP-T range 650–1050°C and 4–12 K bar. The non-ideality can be approximated by temperature-dependent Margules parameters. The retrieved values of ΔH_<T> ^o and ΔH_<T> ^o of exchange reaction between garnet and cordierite and enthalpy and entropy of mixing of Mg-Fe cordierite were combined with recent quaternary (Fe-Mg-Ca-Mn) mixing data in garnet to obtain the geothermometric expressions to determine temperature (T Kelvin): $$\begin{gathered} T(WH) = 6832 + 0.031(P - 1) - \{ 166(X_{Mg}^{Gt} )^2 - 506(X_{Fe}^{Gt} )^2 + 680X_{Fe}^{Gt} X_{Mg}^{Gt} + 336(X_{Ca} + X_{Mn} ) \hfill \\ (X_{Mg} - X_{Fe} )^{Gt} - 3300X_{Ca}^{Gt} - 358X_{Mn}^{Gt} \} + 954(X_{Fe} - X_{Mg} )^{Crd} /1.987\ln K_D + 3.41 + 1.5X_{Ca}^{Gt} \hfill \\ + 1.23(X_{Fe} - X_{Mg} )^{Crd} \hfill \\ \end{gathered} $$ $$\begin{gathered} T(Br) = 6920 + 0.031(p - 1) - \{ 18(X_{Mg}^{Gt} )^2 - 296(X_{Fe}^{Gt} )^2 + 556X_{Fe}^{Gt} X_{Mg}^{Gt} - 6339X_{Ca}^{Gt} X_{Mg}^{Gt} \hfill \\ - 99(X_{Ca}^{Gt} )^2 + 4687X_{Ca}^{Gt} (X_{Mg} - X_{Fe}^{Gt} ) - 4269X_{Ca}^{Gt} X_{Fe}^{Gt} - 358X_{Mn}^{Gt} \} + 640(X_{Fe} - X_{Mg} )^{Crd} \hfill \\ + 1.90X_{Ca}^{Gt} (X_{Mg} - X_{Ca} )^{Gt} . \hfill \\ \end{gathered} $$      

An analysis of 1983 observations of facular contrast with an extreme limb photometer

Analysis of facular contrast I/I _qs from Extreme Limb Photometer (ELP) data of the summer of 1983 yield a mean contrast of 0.91 ± 0.19% and 1.57 ± 0.16% for apertures 1 and 2 located at = 0.198 and at = 0.111, respectively. The ratio of the mean contrast in the outer aperture (closer to the limb) to that of the inner one is 1.71 ± 0.40, indicating an increase in the mean facular contrast toward the limb. This result is in agreement with observations made in 1975, 1979, and 1982. The errors are dominated by the random presence of solar active regions. The combined results from all seasons follow an approximately ^–1 curve. Facular excess solar oblateness signals for 1983 are 33.8 ± 6.6 arc ms and 16.5 ± 2.1 arc ms for ELP apertures 1 and 2, respectively, in reasonable agreement with the 1983 excess solar oblateness results of Dicke, Kuhn, and Libbrecht (1985).     

The Taconite Inlet Lakes Project: a systems approach to paleoclimatic reconstruction

A comprehensive study of meteorological, hydrological, limnological and sedimentological conditions in the watersheds of density-stratified (meromictic) lakes around Taconite Inlet, Northern Ellesmere Island, N.W.T., Canada was carried out from 1990–1992. Lakes C1 and C2 contain seawater trapped by isostatic uplift as the former embayments became isolated from the sea. These lakes, and Lake C3, contain varved sediments which provide an annually resolvable paleoclimatic record. By studing the major systems influencing sedimentation in one of these lakes (Lake C2) a better understanding of the climatic controls on varve formation, and hence on the paleoclimatic signal in the varved sediment record, was obtained. The varves of Lake C2 provide a proxy record of summer temperature for the region.This is the first in a series of papers published in this issue on the Taconite Inlet Lakes Project. These papers were collected by Dr R. S. Bradley.     

The spatial mobility of two generations of young adults in Norway

"This article presents results from a longitudinal study using data from the Norwegian population register, combined with data from the 1970 and 1980 censuses. For two generations, those born in 1948 and 1958, successive migrations are considered and the effects of various sociodemographic characteristics on migratory behaviour are explored....Event-history analysis is used to examine the duration of stay at the place reached at age 22, and the effects of individual characteristics on this duration. Since a distinction is made between intra- and inter-regional migration, it has been possible to show that these effects vary significantly depending on whether we are dealing with short- or long-distance migration."     

Spectroscopic observations of parsamian 21

This work presents spectroscopic observations of Parsamian 21, which has been shown recently by Staude and Neckel to be a fuor-type star. A list of identified absorption lines is given. The results are compared with previous spectroscopic observations over the period 1966–1990. It is shown that the H line profile changed during this period; according to the observations of 1986, the center of the H absorption line was shifted by –140 km/sec from ₀ and reached –600 km/sec at the line edge. It follows from the presented lightcurve that the star has undergone brightness variations of nearly three magnitudes and most likely became a fuor before 1902.Translated fromAstrofizika, Vol. 39, No. 2, pp. 227–235, April–June, 1996.     

Nd,Sr, and Pb isotopic characteristics of Cretaceous intrusive rocks from deep levels of the Sierra Nevada batholith,Tehachapi Mountains,California

The Cretaceous gabbroic to granitic intrusive rocks of the Tehachapi Mountains were emplaced at depths of 25–30 km and thus afford a view of deep processes in the Sierra Nevada batholith. They consist of the 115 Ma Tehachapi suite and the 100 Ma Bear Valley suite; new zircon U-Pb age data reveal the presence of the latter as far west as Grapevine Canyon. The Nd, Sr, Pb, and O isotopic whole-rock data and zircon Pb inheritance patterns for the bulk of the suites suggest an origin by mixing between depleted mantlederived magmas and metasedimentary material with a substantial component of old continental material. However, this mixing is not evident in variations between isotopic ratios and chemical and lithologic parameters. This implies that isotopic hybridization of magmas took place deeper than 30 km, and that fractionation processes are likely responsible for the bulk of the chemical variation in this part of the Sierra Nevada batholith. Consideration of the isotopic data in the context of the Sierra Nevada batholith as a whole suggests that the well-known east-to-west isotopic gradients in the batholith may reflect a change in the average isotopic character of the preintrusive frame-work rather than a change in amount of crustal component. On the other hand, the lack of areal gradients in Sr and Nd isotopic ratios in the main study area may indicate a lack of pronounced gradation at deep levels, at least within the western batholith.     

Compressibility of titanosilicate melts

The effect of composition on the relaxed adiabatic bulk modulus (K₀) of a range of alkali- and alkaline earth-titanosilicate [X ₂ ^n/n+ TiSiO₅ (X=Li, Na, K, Rb, Cs, Ca, Sr, Ba)] melts has been investigated. The relaxed bulk moduli of these melts have been measured using ultrasonic interferometric methods at frequencies of 3, 5 and 7 MHz in the temperature range of 950 to 1600°C (0.02 Pa s < _s < 5 Pa s). The bulk moduli of these melts decrease with increasing cation size from Li to Cs and Ca to Ba, and with increasing temperature. The bulk moduli of the Li-, Na-, Ca- and Ba-bearing metasilicate melts decrease with the addition of both TiO₂ and SiO₂ whereas those of the K-, Rb- and Cs-bearing melts increase. Linear fits to the bulk modulus versus volume fraction of TiO₂ do not converge to a common compressibility of the TiO₂ component, indicating that the structural role of TiO₂ in these melts is dependent on the identity of the cation. This proposition is supported by a number of other property data for these and related melt compositions including heat capacity and density, as well as structural inferences from X-ray absorption spectroscopy (XANES). The compositional dependence of the compressibility of the TiO₂ component in these melts explains the difficulty incurred in previous attempts to incorporate TiO₂ in calculation schemes for melt compressibility. The empirical relationship KV^-4/3 for isostructural materials has been used to evaluate the compressibility-related structural changes occurring in these melts. The alkali metasilicate and disilicate melts are isostructural, independent of the cation. The addition of Ti to the metasilicate composition (i.e. X₂TiSiO₅), however, results in a series of melts which are not isostructural. The alkaline-earth metasilicate and disilicate compositions are not isostructural, but the addition of Ti to the metasilicate compositions (i.e. XTiSiO₅) would appear, on the basis of modulus-volume systematics, to result in the melts becoming isostructural with respect to compressibility.     

Stable isotope study of antimony deposits in the Muratdagi region,western Turkey

The Muratdagi region is rich in antimony deposits having the following common characteristics: post Miocene age, location on the down-thrown blocks next to normal faults, in the vicinity of active or fossil thermal springs, and in contact with carbonate rocks. The isotopic composition of — 7. SMOW of the mineralizing fluid calculated from the measured ° ¹⁸O of quartz and the fluid inclusion microthermometry, is indicative of meteoric water origin. The ° ¹³C of the inclusion CO₂ of — 19.1 to — 25.4 PDB is indicative of interaction with organic material-graphite. The ° ³⁴S of stibnite — 3.6 to — 0.7 is, in view of the mineral assemblage, indicative of magmatic origin of the sulphur. A tightly confined set of structural, lithological, hydrological and geochemical features define a sequence of geochemical processes; formation of acid and reducing fluid, leaching and transport of antimony complexes and precipitation of stibnite within defined lithological units. The set of processes seems to have taken place within a space of 5000 m lateral and 1000 m vertical extension.     

Silicate melts at magmatic temperatures: in-situ structure determination to 1651°C and effect of temperature and bulk composition on the mixing behavior of structural units

The abundance of coexisting structural units in K-, Na-, and Li-silicate melts and glasses from 25° to 1654°C has been determined with in-situ micro-Raman spectroscopy. From these data an equilibrium constant, K_x, for the disproportionation reaction among the structural units coexisting in the melts, Si₂O₅(2Q³)SiO₃(Q²)+SiO₂(Q⁴), was calculated (K_x is the equilibrium constant derived by using mol fractions rather than activities of the structural units). From ln K_x vs l/T relationships the enthalpy (H_x) for the disproportionation reaction is in the range of-30 to 30 kJ/mol with systematic compositional dependence. In the potassium and sodium systems, where the disproportionation reaction shifts to the right with increasing temperature, the H_x increases with silica content (M/Si decreases, M=Na, K). For melts and supercooled liquids of composition Li₂O·2SiO₂ (Li/Si=1), the H_x is indistinguishable from 0. By decreasing the Li/Si to 0.667 (composition LS3) and beyond (e.g., LS4), the disproportionation reaction shifts to the left as the temperature is increased. For a given ratio of M/Si (M=K, Na, Li), there is a positive, near linear correlation between the H_x and the Z/r² of the metal cation. The slope of the H_x vs Z/r² regression lines increases as the system becomes more silica rich (i.e., M/Si is decreased). Activity coefficients for the individual structural units, _i, were calculated from the structural data combined with liquidus phase relations. These coefficients are linear functions of their mol fraction of the form _i=a lnX _i+b, where a is between 0.6 and 0.87, and X _i is the mol fraction of the unit. The value of the intercept, b, is near 0. The relationship between activity coefficients and abundance of individual structural units is not affected by temperature or the electronic properties of the alkali metal. The activity of the structural units, however, depend on their concentration, type of metal cation, and on temperature.