Metabasalts and metagabbros from the Llano Uplift,Texas: Petrologic and geochemical characterization with emphasis on tectonic setting

The 1.0-1.2 b.y. old rocks of the southeastern Llano Uplift, Texas include a 7 km thick sequence of amphibolite-grade, stratified, mafic metasedimentary rock (Packsaddle Schist) which is intruded by a varied suite of syntectonic and late-kinematic intrusions. The metasediments contain large blocks of serpentinized peridotite (Coal Creek serpentinite) and coarse hornblendite and metagabbro. Prior to the end of maximum deformation, the sequence was intruded by low to medium-K₂O tholeiitic basalts (0.40-0.72% K₂O). Late-kinematic low-K₂O tholeiitic basalts (0.38-0.40% K₂O) were intruded as dikes into the folded rocks. The Coal Creek serpentinite contains both syntectonic and late-kinematic low-K₂O tholeiitic metabasalts (0.13–0.36% K₂O). The Llano metabasalts and metagabbros are characterized by low Cr (67–378 ppm) and Ni (36–170 ppm), variable Rb (1.5–14.7 ppm), Sr (140–1229 ppm), TiO₂ (0.40–2.20%), P (568–2707 ppm), and Zr (18–230 ppm), and Y (16–45 ppm), Co (40–57 ppm), and Sc (36–49 ppm) similar to modern MORB. The metabasalts have La abundances from 7 to 39 times chondritic and exhibit light REE enrichment with ¦La/Sm¦_N from 1.13 to 1.45 and ¦La/Yb¦_N from 1.12 to 2.99. The metabasalts show a strong correlation of increasing Zr, Ti, and Y and decreasing Eu/Eu^* (1.56–1.00), CaO/TiO₂, Al₂O₃/TiO₂, and MgO/ MgO+FeO^* with increasing REE enrichment (La_N). The Llano metabasalts and metagabbros have initial ⁸⁷Sr/⁸⁶Sr=0.7029±0.0001. A likely petrogenetic model for these metabasalts is an island arc in which events from early arc development to final late-kinematic intrusion were dominated by tholeiitic volcanism and intrusion. The chemical systematics of the Llano mafic metaigneous rocks suggest they are products of fractionation of olivine, clinopyroxene, and plagioclase from more primitive basaltic magmas generated beneath the island arc complex.     

Petrology and CHIME geochronology of Pan-African high K and Sr/Y granitoids in the Nkambe area, Cameroon

The Central African Belt in the Nkambe area, northwestern Cameroon represents a collisional zone between the Saharan metacraton and the Congo craton during the Pan-African orogeny, and exposes a variety of granitoids including foliated and massive biotite monzogranites in syn- and post-kinematic settings. Foliated and massive biotite monzogranites have almost identical high-K calc-alkaline compositions, with 73–67 wt.% SiO₂, 17–13 wt.% Al₂O₃, 2.1–0.9 wt.% CaO, 4.4–2.7 wt.% Na₂O and 6.3–4.4 wt.% K₂O. High concentrations of Rb (264–96 ppm), Sr (976–117 ppm), Ba (3680–490 ppm) and Zr (494–99 ppm), with low concentrations of Y (mostly< 20 ppm with a range 54–6) and Nb (up to 24 ppm) suggest that the monzogranites intruded in collisional and post-collisional settings. The Sr/Y ratio ranges from 25 to 89. K, Rb and Ba resided in a single major phase such as K-feldspar in the source. Garnet was present in the source and remained as restite at the site of magma generation. This high K₂O and Sr/Y granitic magma was generated by partial melting of a granitic protolith under high-pressure and H₂O undersaturated conditions where garnet coexists with K-feldspar, albitic plagioclase. CHIME (chemical Th–U-total Pb isochron method) dating of zircon yields ages of 569 ± 12–558 ± 24 Ma for the foliated biotite monzogranite and 533 ± 12–524 ± 28 Ma for the massive biotite monzogranite indicating that the collision forming the Central African Belt continued in to Ediacaran (ca 560 Ma).     

Uranium in Phosphorites

The uranium concentration in phosphorites on continents and modern seafloor varies from 0.nto n· 10²ppm (average 75 ppm). The average uranium concentration is 4–48 ppm in Precambrian and Cambrian deposits, 20–90 ppm in Paleozoic and Jurassic deposits, 40–130 ppm in Late Cretaceous–Paleogene deposits, 30–130 ppm in Neogene deposits, and 30–110 ppm in Quaternary (including Holocene) deposits. On the whole, the variation range is almost similar for phosphorites of different ages. The U/P₂O₅ratio in phosphorites ranges from less than unity to 24 · 10^–4(average 3.2 · 10^–4). Major phosphorite deposits of the world with ore reserves of approximately 250 Gt (or 58 Gt P₂O₅) contain up to 19 Mt of uranium. Uranium is present in phosphorites in the tetra- and hexavalent, i.e., U(IV) and U(VI) forms, and their ratio is highly variable. At the early diagenetic stage of the formation of marine phosphorites in a reductive environment, U(VI) diffuses from the near-bottom water into sediments. It is consequently reduced and precipitated as submicroscopic segregations of uranium minerals (mainly uraninite) that are probably absorbed by phosphatic material. During the subsequent reaction between phosphorites and aerated water and the weathering in a subaerial environment, uranium is partly oxidized and lost. The uranium depletion also occurs during catagenesis owing to a more complete crystallization of calcium phosphate and replacement of nonphosphatic components.     

Geochemical and strontium isotopic characteristics of parental Aleutian arc magmas: evidence from the basaltic lavas of Atka

Eighteen flows from a basal stratigraphic sequence on the Aleutian Island of Atka were analyzed for major elements, trace elements and initial ⁸⁷Sr/⁸⁶Sr ratios. Petrographically, these lavas contain abundant plagioclase (24–45%) and lesser amounts of olivine (<7%), magnetite and clinopyroxene phenocrysts. Compositionally, the lavas are high-alumina (20wt%) basalts (48–51 wt% SiO₂) with low TiO₂ (<1%) and MgO (<5%). Within the section, compositional variations for all major elements are quite small. While MgO content correlates with olivine phenocryst contents, no such relationship exists between the other oxides and phenocryst content. These lavas are characterized by 8–10 ppm Rb, high Sr (610–669 ppm), 308–348 ppm Ba and very constant Zr (23–29 ppm) and Sc (23–29 ppm) abundances. Ni and Cr display extremely large compositional ranges, 12–118 ppm and 12–213 ppm, respectively. No correlation exists between trace element concentrations and phenocryst contents. Strontium isotopic ratios show a small but significant range (0.70314–0.70345) and are slightly elevated with respect to typical MORB. No systematic correlation between stratigraphic position and petrography or geochemistry is evident. REE abundances measured on six samples are LREE enriched ((La/ Yb)_N = 2.20–2.81) and display similar chondrite normalized patterns. One sample has a slight positive Eu anomaly but the other lavas do not. Compared to other Aleutian basalts of similar silica content, these lavas are less LREE enriched and have lower overall abundances. The geochemical characteristics of these basalts suggest they represent true liquid compositions despite their highly porphyritic nature. Published phase relations indicate fractionation of a more MgO-rich magma could not have produced these lavas. The high Al₂O₃ and low MgO and compatible element abundances suggest a predominantly oceanic crustal source for parental high-alumina basalts.     

Nickel und Kobalt in Gesteinen des Nördlinger Ries

Zusammenfassung Von Glasbomben aus dem Suevit und kristallinen Gesteinen verschiedener Auswurfbreccien des Rieskraters wurden die Nickel- und Kobaltgehalte bestimmt. Die Gläser enthalten 10,0–51,5 ppm Ni (Mittel von 70 Analysen: 30,1 ppmNi) und 4,8–15,8 ppm Co (Mittel von 50 Analysen: 12,1 ppm Co). Die höchsten Nickel- und Kobaltgehalte finden sich in den nicht rekristallisierten und chemisch unveränderten Bomben des Typ I. Die kristallinen Gesteine des Grundgebirges enthalten 2,5–140 ppm Ni (22 Analysen) und 2,2–29,8 ppm Co (22 Analysen).Die Kobaltgehalte der nicht rekristallisierten Gläser sind ziemlich einheitlich (10,7–15,8 ppm) und ebenso hoch wie diejenigen der kristallinen Gesteine ähnlicher Gehalte an MgO, MgO+FeO+Fe₂O₃ und SiO₂. Die Nickelgehalte der nicht rekristallisierten Gläser dagegen streuen inhomogen über einen größeren Bereich (30,0–51,5 ppm). Sie sind im Mittel höher als die der kristallinen Gesteine mit ähnlichen Gehalten an MgO, MgO+FeO+Fe₂O₃ und SiO₂. Der maximale Unterschied beträgt 25 ppm Ni.

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Ni and Co in rocks from the Nördlinger Ries

Ni and Co have been determined in glass bombs from the suevite and crystalline rocks from different breccia outcrops in the Ries crater. The glasses contain 10.0–51.5 ppm Ni (average of 70 analyses: 30.1 ppm Ni) and 4.8–15.8 ppm Co (average of 50 analyses: 12.1 ppm Co). Highest contents of Ni and Co are to be found in non-recrystallized and chemically unchanged bombs of type I. Crystalline rocks from the basement contain 2.5–140 ppm Ni (22 analyses) and 2.2–29.8 ppm Co (22 analyses).The Co-contents of non-recrystallized glasses are rather uniform (10.7–15.8 ppm) and as high as those of crystalline rocks of similar content of MgO, MgO+FeO+Fe₂O₃ and SiO₂. The Ni-contents of non-recrystallized glasses are inhomogeneously scattered over a larger range (30.0–51.5 ppm). On the average, they are higher than those of crystalline rocks with similar contents of MgO, MgO+FeO+Fe₂O₃ and SiO₂. The maximum difference is 25 ppm Ni.

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Herr Prof. W. von Engelhardt veranlaßte die Bearbeitung dieses interessanten Themas und nahm am Fortgang der Untersuchungen regen Anteil. Herr Dr. D. Stöffler stellte freundlicherweise Probenmaterial zur Verfügung und Herr Dr. H. Puchelt war mir bei analytischen Fragen behilflich. Ihnen allen danke ich für die Förderung dieser Arbeit.     

Geochemical and Sr-Nd-Pb isotopic characteristics of Late Cenozoic leucite lamproites from the East European Alpine belt (Macedonia and Yugoslavia)

In the East European Alpine belt, leucite-sanidine-phlogopite-olivine-bearing volcanic rocks of Late Cenozoic age occur at eight localities within the Vardar suture zone and at one locality in the Southern Carpathian fold-and-thrust belt. Most of these volcanics are characterized by high Mg# (66.6–78.6), high abundances of Ni (117–373 ppm) and Cr (144–445 ppm) as well as high primary K₂O contents (5.63–7.01 %) and K₂O/Na₂O values (1.93–4.91). Rocks with more differentiated compositions are rare. A lamproite affinity of these rocks is apparent from their relatively low contents of Al₂O₃ (9.9–14.3 wt%) and CaO (6.2–8.3 wt%) in combination with high abundances of Rb (85–967 ppm), Ba (1,027–4,189 ppm), Th (18.9–76.5 ppm), Pb (19–54 ppm), Sr (774–1,712 ppm) and F (0.16–0.52 wt%), and the general lack of plagioclase. Although eruption of the magmas took place in post-collisional extensional settings, significant depletions of Nb and Ta relative to Th and La, low TiO₂ contents (0.92–2.17 %), low ratios of Rb/Cs, K/Rb and Ce/Pb as well as high ratios of Ba/La and Ba/Th suggest close genetic relationships to subduction zone processes. Whereas Sr and Nd isotope ratios show relatively large variations (⁸⁷Sr/⁸⁶Sr = 0.7078–0.7105, ¹⁴³Nd/¹⁴⁴Nd = 0.51242–0.51215), Pb isotope ratios display a very restricted range with ²⁰⁶Pb/²⁰⁴Pb = 18.68–18.88 and variable but generally high 7/4 (11–18) and 8/4 (65–95) values. The observed petrographic, geochemical and isotopic characteristics are best explained by a genetic model involving preferential melting of phlogopite-rich veins in an originally depleted lithospheric mantle source, whereby the metasomatic enrichment of the mantle source is tentatively related to the addition of components from subducted sediments during consumption of Tethyan oceanic lithosphere.Editorial responsibility: J. Hoefs     

Comparative geochemistry of volcanics from rift valleys,transform faults and aseismic ridges

New chemical analyses and a review of published data show that there is a compositional diversity between volcanics of basaltic composition found in the M.A.R. rift valley, M.A.R. transform faults and aseismic ridges. The basaltic rocks from the M.A.R. transform faults are less mafic (depleted in olivine content) than those from the M.A.R. rift valley. The transform fault basalts have a higher range of TiO₂ content (1–4%), of Fe₂O₃+FeO content (8–14%) and a lower range of Cr content (50–500 ppm) and Ni content (50–300 ppm). The volcanics from aseismic ridges around the world are considered to be the more felsic types of the two provinces. They have a higher range of variation for their TiO₂ and Fe₂O₃+FeO (1.6–5%; 9–15%; respectively) and a lower range of variability for their Cr and Ni (<250 and 100 ppm respectively) than both the M.A.R. rift valley and transform fault volcanics.It is suggested that transform faults have, by faulting, exposed more fractionated types of basaltic rocks (may be as intrusives) than the rift valley volcanics. While aseismic ridges have undergone a greater degree of differentiation than both transform faults and rift valley volcanics.Contribution n 475 du Département Scientifique, Centre Océanologique de Bretagne Contribution No. 3803 of Woods Hole Oceanographic Institution (USA)     

Petrology of Karoo volcanic rocks in the southern Lebombo monocline, Mozambique

The Karoo volcanic sequence in the southern Lebombo monocline in Mozambique contains different silicic units in the form of pyroclastic rocks, and two different basalt types. The silicic units in the lower part of the Lebombo sequence are formed by a lower unit of dacites and rhyolites (67–80 wt.% SiO₂) with high Ba (990–2500 ppm), Zr (800–1100 ppm) and Y (130–240 ppm), which are part of the Jozini–Mbuluzi Formation, followed by a second unit, interlayered with the Movene basalts, of high-SiO₂ rhyolites (76–78 wt.%; the Sica Beds Formation), with low Sr (19–54 ppm), Zr (340–480 ppm) and Ba (330–850 ppm) plus rare quartz-trachytes (64–66 wt.% SiO₂), with high Nb and Rb contents (240–250 and 370–381 ppm, respectively), and relatively low Zr (450–460 ppm). The mafic rocks found at the top of the sequence are basalts and ferrobasalts belonging to the Movene Formation. The basalts have roughly flat mantle-normalized incompatible element patterns, with abundances of the most incompatible elements not higher than 25 times primitive mantle. The ferrobasalt has TiO₂  4.7 wt.%, Fe₂O_3t = 16 wt.%, and high Y (100 ppm), Zr (420 ppm) and Ba (1000 ppm). The Movene basalts have initial (at 180 Ma) ⁸⁷Sr/⁸⁶Sr = 0.7052–0.7054 and ¹⁴³Nd/¹⁴⁴Nd = 0.51232, and the Movene ferrobasalt has even lower ⁸⁷Sr/⁸⁶Sr (0.70377) and higher ¹⁴³Nd/¹⁴⁴Nd (0.51259). The silicic rocks show a modest range of initial Sr-(⁸⁷Sr/⁸⁶Sr = 0.70470–0.70648) and Nd-(¹⁴³Nd/¹⁴⁴Nd = 0.51223–0.51243) isotope ratios. The less evolved dacites could have been formed after crystal fractionation of oxide-rich gabbroic cumulates from mafic parental magmas, whereas the most silica-rich rhyolites could have been formed after fractional crystallization of feldspars, pyroxenes, oxides, zircon and apatite from a parental dacite magma. The composition of the Movene basalts imply different feeding systems from those of the underlying Sabie River basalts.     

Die Metarodingite der Habachformation,Hohe Tauern (Österreich)

Zusammenfassung Zwei Metarodingitvorkommen aus der Habachformation im nördlichen Vendigermassiv wurden geochemisch und petrologisch untersucht. Die Metarodingite bestehen aus Granat, Klinopyroxen und wechselnden Mengen von Titanit, Ilmenit, Epidot, Chlorit und Calcit und sind von den sie umgebenden Antigoritserpentiniten durch Blackwallbidung getrennt. Sowohl Granat als auch Klinopyroxen sind in zwei Generationen vertreten. Die ältere Generation (Grant, um 95% Grandit-Anteil mit 50–70% Andraditkomponente; Klinopyroxen, Diopsid mit 0,2–0,6% Al₂O₃) entspricht mitT=420°C beiP=2 kb dem niedriggradigen herzynischen Metamorphoseereignis, die jüngere Generation (Granat, und 90% Grandit mit 5% Andraditkomponente; Klinopyroxen, Diopsid mit bis zu 2,5% Al₂O₃), für dieT=480–500°C beiP=5 kb ermittelt werden konnten, entspricht der alpidischen Metamorphose. Mit CaO-Gehalten von bis zu 30 Gew.% und Na₂O- und K₂O-Gehalten von < 0,03 Gew.% sind die Hauptelementchernismen typisch für Rodingite, lassen aber naturgemäß keine Aussage über die Ausgangsgesteine zu. Spurenelement analysen zeigen, daß auch immobile Elemente wie Ti, Zr und Y keine sichere Abletung der Ausgangsgesteine gestatten. Dasselbe gilt für die Verteilung der REE sowie für die Cr-, Co- und Ni-Gehalte, die nur die allgemeine Aussage, daß es sich bei den Ausgangsgesteinen um Gesteine basaltischer Zusammensetzung handelt, zulassen. Stark schwankende, zum Teil sehr hohe W-Gehalte in den Metarodingiten und Blackwalls werden auf Mobilisierungen aus den, die Serpentinite umgebenden Gesteinsserien. zurückgeführt.

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The metarodingites of the Habach Formation, Hohe Tauern, Austria

Summary Geochemical and petrological investigations have been carried out on two occurrences of metarodingites from the Habach Formations within the Venediger massif, Hohe Tauern Austria. The metarodingites consitst of garnet, clinopyroxene and varying amounts of sphene, ilmenite, epidote, chlorite, and calcite. They are surrounded by antigorite-serpentinites from which they are separated by blackwall zones. Garnet and clinopyroxene are present in two generations. The older one (garnet with about 95% grandite content and 50–70% andradite; diopside with 0,2–0,6% Al₂O₃) represents the low grade Hereynian metamorphic event with an equilibration temperature of 420°C atP=2 kb. The younger generation (garnet with about 90% grandite and 5% andradite; diopside with up to 2.5% Al₂O₃) is of Alpine age and could be fixed atT=480–500°C andP=5 kb. The main element contents are typical for rodingites and show CaO-concentrations up to 30% and K₂O- as well as Na₂O-concentrations of less than 0.03%. Trace element analyses indicate that even immobile elements like Ti, Zr and Y do not allow a clear reconstruction of the original rocks from which the rodingites are derived. The same holds true for the distribution of REE-patterns and the contents of Cr, Co, and Ni. However, a primary basattic composition of the original rocks can be deducted. Additionally, there are varying, in part very high W-contents (up to 2.7% WO₃) in the metarodingites and the blackwall zones which are certainly derived by mobilisation from the surrounding rocks.

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Mit 6 Abbildungen     

Multistage Metamorphic Evolution of the Trivandrum Granulite Block, Southern India

The Trivandrum Granulite Block (TGB), southern India records evidence for three distinct stages of evolution (M1–;M3) during the Pan-African high grade metamorphism, with possible temperature gradient from north to south of the terrain as detected from mineral phase equilibria thermobarometry in three classic localities, namely Nuliyam, Kunnanpara and Nellikkala. The charnockites, both incipient and massive, were formed during the first stage (M1) at temperatures higher than their host rocks, and at appreciably lower pressures. Charnockite formation was dominantly controlled by an increase in partial pressure of CO₂, along structural locales during subisothermal decompression, although an increase of potash activity could have also been an important factor in this process. The charnockites at Nellikkala in the northern margin of TGB were formed under appreciably more H₂O-rich conditions (X_H2O = 0.53±0.03) than those at Nuliyam (X_H2O = 0.25±0.02) in the southern margin. It is inferred that during the period between the metamorphic stages M1 and M2, the terrain experienced subisobaric cooling. Comparison of results from thermobarometry with data on absolute age determinations from geochronology of the metamorphic rocks in TGB allows the interpretation that the M1 metamorphic event took place during 540–;600 Ma, M2 at about 530 Ma and M3 in the interval of 440–;470 Ma. Mineralogic and thermobarometric evidence for earlier high-grade metamorphic processes, if any, have been erased from these rocks. The processes of charnockite formation and post-peak retrograde metamorphism in the TGB took place under high geothermal gradients (40–;150°/km). This probably testifies to the existence of a local heat source, either magmas at depth or mantle (plume) beneath the region. The general metamorphic cycle in the TGB is estimated to be ca. 100–;160 Ma, which is much shorter in time span than that in the other regions of southern Peninsular India such as the Karnataka Craton and the Eastern Ghats Mobile Belt. During this period, the terrain experienced rapid exhumation of approximately 6–;7 cm/year, with the total amplitude of vertical movements estimated to be about 16–;17 km.     

Elemental and Sr–Nd isotopic systematics of the early Mesozoic volcanic sequence in southern Jiangxi Province, South China: petrogenesis and tectonic implications

Elemental and Sr–Nd isotopic results are presented for the early Mesozoic volcanic sequence (~172 Ma) in southern Jiangxi Province, South China. The sequence is voluminously composed of ~45% subalkaline basaltic rocks (group 1), <5% high-mg andesite–dacites (group 2) and ~50% rhyolites (group 3). The group 1 rocks are characterized by (La/Yb)_cn = 3.8–7.2, Eu/Eu* = 0.65–1.15, Nb/La = 0.64–0.99, ⁸⁷Sr/⁸⁶Sr(t) = 0.70602~0.70822 and _Nd(t) = –1.63 to +0.11, similar to those of an EMII-like source. The group 2 rocks have mg=0.42~0.60, SiO₂=60.24~66.71%, MgO=2.65~ 5.54%, Ni=24~102 ppm and Cr=84~266 ppm, classified as high-mg andesitic rocks. These rocks are more enriched in LILEs and LREE with more significant negative Eu anomaly (0.63~0.79), are more depleted in HFSEs with Nb/La ratios of 0.40–0.56 and have lower _Nd(t) (–9.44 to –7.78) and higher ⁸⁷Sr/⁸⁶Sr(t) (0.70985~0.71016), in comparison with the group 1 rocks. They most likely originated from metasomatised veins in the lithospheric mantle. The origination of the group 1 and group 2 magma suggests the development of a peridotite-plus-vein lithospheric mantle during early Mesozoic era beneath the interior of the Cathaysian block. The group 3 rhyolites are characterized by high SiO₂ (72.75~77.97%), Zr (99~290 ppm), Hf (3.9~9.7 ppm) and Ga/Al (2.76~3.87) and significant Nb–Ta, Ba–Sr and P–Ti depletions. These rhyolites exhibit Sr–Nd isotopic compositions (⁸⁷Sr/⁸⁶Sr(t) = 0.70962~0.71104, _Nd(t) = –4.63 to –5.80) similar to the contemporaneous Zhaibei and Pitou A-type granites in the area. Such characteristics suggest that they might be derived from the underplating basaltic magma contaminated by crustal materials. Therefore, an early Mesozoic rifting model in response to intracontinental lithospheric extension is proposed to account for the early Mesozoic volcanism in southern Jiangxi Province, South China.     

The geochemistry and petrogenesis of the lavas of the Vulsinian District,Roman province,Central Italy

The Vulsinian lavas are dominated by a suite of undersaturated leucite-bearing basic to intermediate compositions. The remaining lavas are mainly oversaturated and have shoshonitic affinities. One hundred and thirty-five samples have been analysed for major elements and most for 20 trace elements. Twenty-seven lavas have been analysed for REE. They are all perpotassic (for the undersaturated lavas: K₂O/Na₂O=2–8) and have very high LIL element concentrations, (e.g. Rb=400–800 ppm, Th=25–150 ppm, REE/REE_cho=c.200, (LREE/HREE)_cho=c.20) even in the most basic rocks.The undersaturated lavas appear to be interrelated by fractional crystallization of cpx±olivine (from 14 to 11 wt.% CaO), cpx+leu±plg±mica (from 11 to 8 wt.% CaO), cpx+leu+plg+apa+magnetite±mica (from 8 to 5 wt.% CaO), and additional sanidine (or hyalophane)±haüyne (from 5 to 3 wt.% CaO). The saturated lavas and the few slightly undersaturated shoshonite basalts are thought to be evolved from the undersaturated magma(s) by crustal contamination or mixing with silica-rich magmas. The parental Vulsinian magma having: Mg-value=c.73, Cr=300–700 ppm, Ni=100–125 ppm, Sc= 40–50 ppm, Fo_89–92, Di_77–97 approximates a primary, mantle-derived liquid. Enrichment in LIL elements (incl. REE) and LREE/HREE suggest a small degree of partial melting from fertile mantle; whereas the low concentrations of Na, Ti and P suggest larger degrees of partial melting. This indicates that either the primary magma or the parental mantle was metasomatized by a fluid, which previously equilibrated with subducted continental material. This model agrees with published high ¹⁸O, high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd.     

Variations in the OH concentration of rutiles from different geological environments

Summary A suite of 19 rutiles form a wide range of geological environments shows a distinct variability in the OH concentrations. The analytical H₂O⁺ content determined by IR spectroscopy varies from 0.04 to 0.21 wt.% with the greatest amounts occurring in amphibolite facies rutiles. The main feature of the IR spectra in the region of the OH stretching fundamental is a single narrow band centered at 3280 cm^–1; some of the spectra show an additional band, centered either at 3360 or at 3320 cm^–1. Varying OH concentrations in rutiles are probably a function of the activity of hydrous components during crystallization and are weakly correlated to a minor content of tri- and pentavalent elements.

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Die Variation in der OH Konzentration von Rutilen unterschiedlicher geologischer Vorkommen

Zusammenfassung Eine Serie von 19 Rutilen aus unterschiedlichen geologischen Vorkommen zeigt eine deutliche Variabilität in den OH Konzentrationen. Der IR spektroskopisch bestimmte analytische H₂O⁺-Gehalt variiert von 0.04 bis 0.21 Gew.%, wobei die höchsten Gehalte in Rutilen der Amphibolitfacies auftreten. Das wesentliche Merkmal der IR Spektren im Bereich der OH Streckschwingung ist eine einzelne schmale Bande bei 3280 cm^–1; einige der Spektren zeigen entweder bei 3360 oder bei 3320 cm^–1 eine zusätzliche Bande. Wahrscheinlich stellen die variierenden OH Konzentrationen, die mit einem geringen Gehalt an drei- und fünfwertigen Elementen schwach korreliert sind, eine Funktion der Wasser-Aktivitäten bei der Kristallisation dar.

     

Die Kristallstruktur von Denningit, (Mn,Ca,Zn) Te2O5. Ein Beispiel für die Koordination um vierwertiges Tellur

Zusammenfassung Denningit, (Mn, Ca, Zn) Te₂O₅ ist tetragonal mit der Raumgruppe P 4₂/n bc und den Gitterkonstanten a=8,82, c=13,04; Z=8. Die Struktur wurde mit Patterson-, Fourier- und (F_o-F_c)-Projektionen parallel [100], [110] und [001] bestimmt und verfeinert. Abschließend konnte eine least-squares-Verfeinerung durchgeführt werden. Je zwei trigonale TeO₃-Pyramiden (Te–O=1,84–2,04 ) sind zu isolierten Te₂O₅-Gruppen verbunden. Mn, Ca und Zn in 8- und in [4+2]-Koordination bilden längs [001] Ketten, die durch Te₂O₅-Gruppen miteinander verknüpft sind.

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Summary Denningite, (Mn, Ca, Zn) Te₂O₅ is tetragonal with spacegroup P 4₂/n bc and unit-cell dimensions a=8,82, c=13,04; Z=8. The structure has been determined and refined by Patterson, Fourier and (F_o-F_c) projections along [100], [110] and [001]. Finally a least-squares refinement has been carried out. Pairs of trigonal TeO₃ pyramids (Te–O=1,84–2,04) are connected to isolated Te₂O₅ groups. Mn, Ca and Zn in 8 coordination and in [4+2] coordination form chains along [001] connected by Te₂O₅ groups.

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Mit 3 Textabbildungen

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Herrn Professor Dr.F. Machatschki zum 70. Geburtstag gewidmet     

Evolving fluid composition during prograde metamorphism in subduction zones: A new approach using carbonate-bearing assemblages in the pelitic system

The changing XCO₂ in fluids during the progressive metamorphism in Sanbagawa belt of the Cretaceous subduction zone, Japan, was estimated by a newly proposed method. The subduction zone meta-sediments are characterized commonly by four-phase assemblages in the CaO–NaAlO₂–KAlO₂–Al₂O₃ system with excess quartz and a CO₂–H₂O binary fluid phase. Using the common assemblage of calcite–albite–muscovite–clinozoisite, XCO₂ of the fluid was estimated to be from about 0.0001–0.0005 (the lowest grade chlorite zone), through 0.004–0.01 (garnet zone), 0.01–0.05 (albite–biotite zone) to 0.06–0.2 (oligoclase–biotite zone).The paragenetic relationship of meta-sediments from the subduction zones was compared in a wide P–T range to cover the stability fields of aragonite and jadeite. As a result, an excellent P–T–XCO₂ relationship was delineated to serve as a quantitative monitor for the evolving fluid composition during the progressive metamorphism in subduction zones.     

Petrology,isotope characteristics,and K-Ar ages of the Maranhão,northern Brazil,Mesozoic basalt province

Northern Brazil contains remnants of Mesozoic flood basalts and hypabyssal rocks that were apparently emplaced during tectonism related to opening of the Atlantic Ocean. Analyses and new K-Ar ages reveal that this 700x250 km Maranhão province (5°–8°S) has low-Ti basalts (1.1 wt% TiO₂) in the western part that range about 160 to 190 Ma, and high-Ti basalts (3.4–4.4 wt% TiO₂) in the eastern part about 115–122 Ma. Low-Ti basalt compositions are less evolved and have a smaller range, Mg# 62-56, than the high-Ti basalts, Mg# 44–33. General characteristics of the least evolved members of low- and high-Ti groups include, respectively, Zr 100 and 250 ppm, Sr 225 and 475 ppm, Ba 200 and 500 ppm, Nb 10 and 26 ppm, Y 29 and 36 ppm, La/Yb_(n) 4.2 and 8.8, where La_(n) is 30 and 90. Overall compositions resemble the low- and high-Ti basaltic rocks of the Mesozoic Serra Geral (Paraná) province in southern Brazil. The Maranhão low-Ti basalts have more radiogenic Sr and Pb and higher ¹⁸O than the high-Ti basalts. Respectively, low- vs high-Ti: _Sr26–54 vs 15–18; ²⁰⁶Pb/²⁰⁴Pb=18.25–.78 vs 18.22–.24; and ¹⁸O 8.9–12.6 vs 6.5–8.6. Nd isotopes overlap: _Nd–1.6 to –3.8 vs –2.1 to –3. Ages, compositions, and isotopes indicate that the low- and high-Ti groups had independent parentages from enriched subcontinental mantle. However, both groups can be modeled from one source composition if low-Ti basalt isotopes reflect crustal contamination, and if the parentages for each group were picritic liquids that represent either higher (for low-Ti) or lower (for high-Ti) percentages of melting of that single source. When comparing Pb isotopes of Maranhão and Serra Geral high-Ti basalts (uncontaminated) to evaluate the DUPAL anomaly, Maranhão has Pb 7/4=4.6–11, and Pb 8/4=72–87; Serra Geral has Pb 7/4=10–13, and Pb 8/4=95–125. The small difference is not enough to conform to DUPAL contours, and is inconsistent with large-scale isotopic heterogeneity of mantle beneath Brazil prior to rifting of South America from Africa. Maranhão low-Ti magmas probably relate to the opening of central North Atlantic, and high-Ti magmas to the opening of equatorial Atlantic. The proposed greater percentage of source melting for low-Ti basalts may reflect a Triassic-Jurassic hotspot, while lesser melting for high-Ti magmas may relate to Cretaceous decompressional (rifting) melting.     

Monazite solubility and dissolution kinetics: implications for the thorium and light rare earth chemistry of felsic magmas

A series of monazite dissolution experiments was conducted in a hydrous (1–6 wt.%) granitic melt at 8 kbar over the temperature range 1,000–1,400° C. A polished cube of monazite was immersed in a natural obsidian melt and allowed to partially dissolve. Electron microprobe traverses perpendicular to the crystal-melt interface revealed concentration gradients in the LREEs and P. Diffusivities of the LREEs and P were calculated from these profiles, yielding the following Arrhenius relations for the LREEs: D=0.23 exp(–60.1 kcal mol^–1/RT) at 6% water D=2.30×10⁷ exp(–122.1 kcal mol^–1/RT) at 1% water These results demonstrate the importance of dissolved water on REE diffusion. Phosphorus diffusivities are nearly identical to those of the rare-earths, suggesting that P diffusion charge-compensates REE diffusion. The concentration of LREEs required for monazite saturation in these melts is given by the level of dissolved LREEs at the crystal-melt interface. These values also show a dependence on dissolved water, with LREE_sat=60 ppm at 6% H₂O when extrapolated down to 700° C, and LREE_sat=30 ppm at 1% H₂O. Calculated dissolution rates based on the above parameters indicate that minute (<30 m diameter) monazite crystals will be readily digested by an enclosing anatectic magma under reasonable geologic conditions (i.e., T=700–800° C and >2% H₂O), whereas larger (> 50 m) crystals will likely be residual over the duration of an anatectic event. The low solubility of monazite in this melt suggests that the LREE depletion observed in some felsic differentiation suites may be the result of monazite crystallization. Limited experimental and geochemical/petrologic evidence indicates that compositional changes in the melt accompanying differentiation decrease the solubility of monazite drastically. Kinetic and chemical constraints may also lead to localized monazite saturation and inclusion in major phases or even other accessories. Variations in the REE composition of monazite from different parageneses probably reflects the REE pattern of the parent melt, and may be due to gradational differences in the stability of individual or subgroup REE-complexes as a function of melt composition. Particularly important in this regard seems to be the lime+alkali/alumina balance of the melt and its volatile content.     

The crystal structure of scotlandite,PbSO3

Summary The crystal structure of scotlandite —a=4.505(2),b=5.333(2),c=6.405(6) Å, =106.24(3)^o; space groupP2₁/m; cell content 2 {PbSO₃} — was determined from singlecrystal X-ray diffractometer data. Scotlandite is isotypic with molybdomenite, PbSeO₃. Lead is coordinated to nine oxygen atoms with Pb-O_av=2.75 Å, and possibly further to one sulphur atom with Pb–S=3.46 Å. The average S–O distance in the pyramidal SO₃ group is 1.52 Å. The structural relationships to cerussite, PbCO₃, are discussed.

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Die Kristallstruktur des Scotlandits, PbSO₃

Zusammenfassung Die Kristallstruktur des Scotlandits —a=4,505(2),b=5,333(2),c=6,405(6) Å, =106,24(3)^o; RaumgruppeP2₁/m; Zellinhalt 2 {PbSO₃} — wurde aus Einkristall-Röntgendiffraktometerdaten bestimmt. Scotlandit ist mit Molybdomenit, PbSeO₃, isotyp. Blei wird von neun Sauerstoffatomen mit Pb–O_av=2,75 Å und möglicherweise zusätzlich von einem Schwefelatom mit Pb–S=3,46 Å koordiniert. Der durchschnittliche S–O-Abstand in der pyramidalen SO₃-Gruppe mißt 1,52 Å. Die strukturellen Beziehungen zu Cerussit, PbCO₃, werden diskutiert.

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With 2 Figures     

Geochemistry and origin of massif-type anorthosites

Samples of Proterozoic anorthosite complexes from the Adirondack Mountains of New York, Burwash Area of Ontario, and the Nain Complex of Labrador, ranging in composition from anorthosite to anorthositic gabbro, have been analyzed for major elements, Rb, Sr, Ba and nine rare-earth elements (REE), in order to set limits on the compositions and origins of their parent magmas. Similar rock types from the different areas have similar major and trace element compositions. The anorthosites have high Sr/Ba ratios, low REE abundances (Ce about 10, Yb about 0.5–1.5 times chondrites) and large positive Eu anomalies. The associated anorthositic gabbros have lower Sr/Ba ratios, REE abundances nearly an order of magnitude higher than the anorthosites, and small to negligible positive Eu anomalies.Model calculations using the adcumulate rocks with the lowest REE abundances and published distribution coefficients yield parent liquids having REE abundances and patterns similar to those of the associated anorthositic gabbros with the highest REE abundances. Rocks with intermediate REE abundances are the result of incorporation of a liquid component by a plagioclase-rich cumulate similar to the adcumulate samples. The analytical data and model calculations both suggest parent liquids having compositions of 50–54% SiO₂, greater than 20% Al₂O₃, about 1% K₂O, atomic Mg/(Mg+Fe²⁺) ratios (Mg No.'s) of less than 0.4, 15–30 ppm Rb, 400–600 ppm Sr and 400–600 ppm Ba, 40–50 times chondrites for Ce and 8–10 times chondrites for Yb.The low atomic Mg/(Mg+Fe²⁺) values for these rocks combined with geophysical evidence suggesting there are not large quantities of ferromagnesian material at depth, indicate that the anorthositic masses are not products of fractional crystallization of mafic melt derived from melting of the mantle. Rather, it is suggested that they are a result of partial melting of tholeiitic compositions at depths shallower than the basalt-eclogite transformation, leaving a pyroxene-dominated residue.     

Refractory- and metallurgical-type chromite ores,Zambales ophiolite,Luzon, Philippines

The Zambales ophiolite is the major source of chromite ore in the Philippines. The chromitites are concordant cumulates and are associated with distinct chromitite-bearing sequences within the mantle peridotites. Refractory and metallurgical chromite deposits are spatially separated and related to different lithologic associations, which crystallized from different parental magmas. — Refractory chromite ores (30–44 wt% Cr₂O₃; 20–30 wt% Al₂O₃) are linked with the peridotite-troctolite-olivine gabbro lineage. Two main types were found: (1) Al-rich refractory ores associated with harzburgites and feldspathic periodotites and (2) more Cr-rich varieties associated with lherzolites. — Metallurgical chromite ores (45–53 wt% Cr₂O₃; 12–18 wt% Al₂O₃) are linked with the peridotite-pyroxenite-norite lineage. Two main types were also found: (1) Cr-rich metallurgical ores associated with orthopyroxenites and (2) more Al-rich varieties related to clinopyroxenites. — The chemical composition of chromite within the deposits varies depending on the chromite/silicate ratios of the ore types and grades continuously into accessory chrome spinels in the wall-rock peridotites. — The geochemistry of accessory chrome spinels in various peridotites and mafic cumulates depends on the mineralogical composition and the stratigraphic position of their host rocks.New address: BEB Erdgas und Erdöl GmbH, Riethorst 12, D-3000 Hannover 51The terms chrome-spinels and chromite are used as follows: 1. Chrome-spinel is only used for those occuring as accessory minerals in various ultramafic and mafic rocks (= accessory chrome-spinels). Their chemical composition has been determined only by microprobe analysis. — 2. Chromite is used for ore and ore deposits (=chromitites); the chemical composition has been determined by wet chemistry (AAS) or by microprobe analysis