A Back-arc Palaeotectonic Setting for the Augaro Neoproterozoic Magmatic Rocks of Western Eritrea

The Augaro volcano-sedimentary assemblages of western Eritrea are part of the Neoproterozoic, N-S trending belt of low-grade volcano-sedimentary and associated plutonic rocks. In contrast to the volcanic-dominated oceanic-arc assemblages in central Eritrea, the predominant rock types in the west are supracrustal sequences of sedimentary origin with subordinate volcanic rocks. These Augaro supracrustal rocks are overlain, unconformably, by a basin-fill metasedimentary succession known as the Gulgula Group. The Augaro metavolcanic rocks are tholeiitic and range in composition from basalt to basaltic andesite. Comparison of trace element characteristics and N-MORB-normalised spidergrams of these rocks with those of modern volcanic environments and age-comparable metavolcanic rocks of known tectonic association from the Arabian-Nubian Shield suggest that the volcanic assemblages from western Eritrea were generated in a back-arc tectonic setting.

Single zircon Pb-Pb evaporation and vapour-transfer U-Pb analyses of magmatic zircons from pre/syn-tectonic granites yield a mean ²⁰⁷Pb/²⁰⁶Pb age of 849±20 Ma and an upper concordia intercept age of 849±26 Ma. These ages are interpreted to represent the time of major magmatism in western Eritrea and are comparable to ages of early arc magmatism in central and northern Eritrea and in the southern Nubian Shield. Initial eNd values and initial Sr isotope ratios of whole-rock samples of magmatic rocks calculated for an age of 850 Ma range from +4.0 to +7.1 and 0.7026 to 0.7037, respectively. Single zircon ²⁰⁷Pb/²⁰⁶Pb ages, initial eNd value and Sr isotope ratio for a granitic clast in the Gulgula metaconglomerate suggest that the source area for the Gulgula metasedimentary rocks is similar to the surrounding Neoproterozoic rocks of western Eritrea.     

Deglacial paleoclimate in the southwestern United States: an abrupt 18.6 ka cold event and evidence for a North Atlantic forcing of Termination I

We present a new U-series dated speleothem record (PC-1) from the Great Basin that documents deglacial climate variability between ca 20.1 and 15.6 ka. Our data show an abrupt 18.6 ka cold event preceding Heinrich event 1 that is consistent with expansion of the Laurentide Ice sheet during the ‘binge’ phase of ice growth. This event coincided with dessication of pluvial Lake Mojave suggesting cold and dry conditions in the southern Great Basin at this time. PC-1 δ¹⁸O values before and during Heinrich event 1 are similar, but an increase in stalagmite growth rates suggests wetter conditions that coincided with deposition of spring deposits in southern Nevada. The time interval of our record is consistent with the timing of pluvial conditions in the Great Basin as evident from a comparison to regional wetness proxies. Our new speleothem record, recovered from the recharge area for Devils Hole, does not show a δ¹⁸O increase coincident with the abrupt increase in Devils Hole δ¹⁸O at c. 18 ka, challenging the view that the Great Basin experienced an early Termination I. This hypothesis is supported by two other southwest speleothem records that demonstrate deglaciation was synchronous with forcing from the North Atlantic Ocean. We suggest that Devils Hole speleothem δ¹⁸O values may partly reflect source water changes in the regional aquifer. Further, Devils Hole δ¹³C minima coincide with peak global glacial conditions and weak Asian monsoon periods, suggesting that they constrain better the timing of pluvial conditions in the Great Basin.     

Experimental evaluation of anaerobic digestion for coffee wastewater treatment and its biomethane recovery potential

The objective of this study was to evaluate the performance of anaerobic digestion (AD) as an eco-friendly technology for coffee wastewater (CWW) management. First, we have characterized the CWW and found that it is suitable for microbial degradation with pH adjustment. Then, we designed a simple anaerobic batch reactor (ABR) and evaluated its potential for energy yield and efficiency to remove pollutants. The experiment was carried out by operating the anaerobic digestion (AD) for 70 days. The ABR was found to be efficient for the removal of organic load (90 %), nutrients (82 %) and suspended solids (95 %) from coffee processing waste. The increased removal efficiency of pollutants was dependent on the hydraulic retention time of the system. We also estimated that the coffee waste has a potential to produce a theoretical energy yield of 4–10 million KJ/day and an organic fertilizer (digestate) of 18.8–25.2 kg VSS/day. As a result, the AD would be a more sensible consideration as an eco-friendly treatment option for the coffee waste. The use of AD for CWW treatment not only reduces emission of greenhouse gases to the environment but also circumvents the rising demand for fuel wood and charcoal that causes a severe deforestation in the coffee growing regions of the world.     

Subduction and melting processes inferred from U-Series, Sr-Nd-Pb isotope, and trace element data, Bicol and Bataan arcs, Philippines

We present U-series, Sr-Nd-Pb isotope, and trace element data from the two principal volcanic chains on Luzon Island, developed over oppositely dipping subduction zones, to explore melting and mass transfer processes beneath arcs. The Bataan (western) and Bicol (eastern) arcs are currently subducting terrigenous and pelagic sediments, respectively, which have different trace element and isotopic compositions. The range of (²³⁰Th/²³⁸U) disequilibria for both arcs is 0.85-1.15; only lavas from Mt. Mayon (Bicol arc) have ²³⁰Th activity excesses. Bataan lavas have higher ⁸⁷Sr/⁸⁶Sr and lower ¹⁴³Nd/¹⁴⁴Nd than Bicol lavas (⁸⁷Sr/⁸⁶Sr = 0.7042-0.7046, ¹⁴³Nd/¹⁴⁴Nd = 0.51281-0.51290 vs. ⁸⁷Sr/⁸⁶Sr = 0.70371-0.70391, ¹⁴³Nd/¹⁴⁴Nd = 0.51295-0.51301) and both arcs show steep linear arrays towards sediment values on ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagrams. Analysis of incompatible element and isotopic data allows identification of a sediment component that, at least in part, was transferred as a partial melt to the mantle wedge peridotite. Between 1% and 5% sediment melt addition can explain the isotopic and trace element variability in the rocks from both arcs despite the differences in sediment supply. We therefore propose that sediment transfer to the mantle wedge is likely mechanically or thermally limited. It follows that most sediments are either accreted, reside in the sub-arc lithosphere, or are recycled into the convecting mantle. However, whole-sale sediment recycling into the upper mantle is unlikely in light of the global mid-ocean ridge basalt data. Fluid involvement is more difficult to characterize, but overall the Bicol arc appears to have more fluid influence than the Bataan arc. Rock suites from each arc can be related by a dynamic melting process that allows for ²³⁰Th ingrowth, either by dynamic or continuous flux melting, provided the initial (²³⁰Th/²³²Th) of the source is ∼0.6-0.7. The implication of either model is that inclined arrays on the U-Th equiline diagram may not have chronologic significance. Modeling also suggests that U-series disequilibria are influenced by the tectonic convergence rate, which dictates mantle matrix flow. Thus with slower matrix flow there is a greater degree of ²³⁰Th ingrowth. While other factors such as prior mantle depletion and addition of a subducted component may explain some aspects of U-series data, an overall global correlation between tectonic convergence rate and the extent of U-Th disequilibria may originate from melting processes.     

Crust-mantle interaction in continental arcs: inferences from the Mesozoic arc in the southwestern United States

Arc magmas ranging in composition from basaltic andesites to rhyolites and intrusive equivalents were emplaced into the western margin of the North American craton starting in Late Triassic time giving way to rift0related sedimentation in the Late Jurassic. The region of this study cuts across Proterozoic basements of contrasting Nd model ages, 1.7–1.8 Ga (average ɛ_Nd∼−11) in eastern Arizona and 2.0 to 2.3 GA (average ɛ_Nd∼−18) in western Arizona and eastern California (Bennett and DePaolo 1987). The Mesozoic rocks have initial ɛ_Nd of -3.4 to-6.4 in the eastern part of the study area and -7.1 to -9.2 in the western part. All of the rocks have elevated ⁸⁷Sr/⁸⁷Sr initial ratios (>0.706). Trends in initial ɛ_Nd values of Mesozoic arc rocks are directly correlated with the Nd model ages of the basement through which they passed. Simple two-component mixing calculations indicate that recycled continental crust in the arc magmas represents on average about 65%. A minimum of 35% mantle input into continental arc magmas, as recent as the Mesozoic, represents a significant contribution to the growth of the continental crust, in the absence of a return flow of continental material into the mantle of similar magnitude. In a detailed study in the Santa Rita Mountains. Arizona, there is a pattern of increase of ɛ_Nd with time: early basaltic andesites have more negative ɛ_Nd than later felsic rocks. A correlated pattern of depletion with time is also observed with trace element and major element data. We attribute this either to progressive hybridization of the lower crust by repeated injection of mantle magmas, or the progressive thinning of the continental crust during prolonged arc magmatism. The present data do not allow distinction between the two models. Progressive decrease in crustal contribution to arc magmas with time may be an important feature of continental arc evolution. Hybridization of the lower crust due to repeated injection of mantle melts during arc magmatism may help contribute to small-scale heterogeneities in lower crust inferred from seismic and xenolith data. Similarly, whether there is a well defined MOHO or sharp crust-mantle boundary in any given segment of the continental crust may in part depend on the extent of crust modification as a result of continental arc magmatism.     

Thallium: A potential guide to mineral deposits

Several recent studies have suggested that rocks associated with mineral deposits of hydrothermal origin are generally enriched in Rb. TI is similar in its geochemical characteristics to Rb, but its use as a potential guide to ore deposits has not been suggested. Although TI has the same size and valency as Rb, it is concentrated more in residual melts than Rb and K because the TI-O bond is more covalent and weaker than either the Rb-O or K-O bonds.A new method which is rapid and precise has been developed by one of the authors for the determination of TI in geological materials at the ppb level. About 350 rocks from 4 mineralized areas in northeastern Washington and central Montana were analyzed for TI by this method. Most of these rocks were also analyzed for SiO₂, A1₂O₃,Fe₂O₃, MgO, CaO, Na₂O, K₂O, TiO₂, P₂O₅, MnO, Ag, As, Au, Ba, Co, Cu, F, Li, Mo, Ni, Pb, Sr, Sb, Sn, Sr, Te, U, W, and Zn. The ore deposits of the areas studied include the gold-silver deposits of the Republic district, the uranium deposit of the Midnite mine, the coppermolybdenum deposit of Mount Tolman, and the gold deposits of the North Moccasin mining district.In all the mineralized areas there is significantly more TI in hydrothermally altered rocks than in unaltered rocks. The very high abundance of TI in the altered rocks of the North Moccasin gold district, and the significant positive correlations of TI and K and TI and Rb in the mineralized rocks of the other three areas suggest that TI was concentrated in hydrothermal fluids. In altered rocks the average K/Rb and K/TI ratios are lower, and the Rb/Sr and TI/Sr ratios are higher.Often the abundance of TI and the K/TI and TI/Sr ratios are more useful in delineating mineralized areas than the abundance of Rb and the K/Rb and Rb/Sr ratios. The ternary relationships between TI and several other elements, especially Rb, K, Ba, and Sr, show mineralized rocks to fall near the TI apices or near the TI-Rb or TI-K boundaries.     

Stable isotope variations in modern tropical speleothems: Evaluating equilibrium vs. kinetic isotope effects

Applications of speleothem calcite geochemistry in climate change studies require the evaluation of the accuracy and sensitivity of speleothem proxies to correctly infer paleoclimatic information. The present study of Harrison’s Cave, Barbados, uses the analysis of the modern climatology and groundwater system to evaluate controls on the C and O isotopic composition of modern speleothems. This new approach directly compares the δ¹⁸O and δ¹³C values of modern speleothems with the values for their corresponding drip waters in order to assess the degree to which isotopic equilibrium is achieved during calcite precipitation. If modern speleothems can be demonstrated to precipitate in isotopic equilibrium, then ancient speleothems, suitable for paleoclimatic studies, from the same cave environment may also have been precipitated in isotopic equilibrium. If modern speleothems are precipitated out of isotopic equilibrium, then the magnitude and direction of the C and O isotopic offsets may allow specific kinetic and/or equilibrium isotopic fractionation mechanisms to be identified.Carbon isotope values for the majority of modern speleothem samples from Harrison’s Cave fall within the range of equilibrium values predicted from the combined use of (1) calcite-water fractionation factors from the literature, (2) measured temperatures, and (3) measured δ¹³C values of the dissolved inorganic carbon of drip waters. Calcite samples range from ∼0.8‰ higher to ∼1.1‰ lower than predicted values. The ¹³C depletions are likely caused by kinetically driven departures in the fractionation between HCO₃⁻ (aq) and CaCO₃ from equilibrium conditions, caused by rapid calcite growth. ¹³C enrichments can be accounted for by Rayleigh distillation of the HCO₃⁻ (aq) reservoir during degassing of ¹³C-depleted CO₂.Modern speleothems from Harrison’s Cave are not in O isotopic equilibrium with their corresponding drip waters and are 0.2‰ to 2.3‰ enriched in ¹⁸O relative to equilibrium values. δ¹⁸O variations in modern calcite are likely controlled by kinetically driven changes in the fractionation between HCO₃⁻ (aq) and CaCO₃ from equilibrium conditions to nonequilibrium conditions, consistent with rapid calcite growth. In contrast to δ¹³C, δ¹⁸O values of modern calcite may not be affected by Rayleigh distillation during degassing because CO₂ hydration and hydroxylation reactions will buffer the O isotopic composition of the HCO₃⁻ (aq) reservoir. If the effects of Rayleigh distillation manifest themselves in the O isotopic system, they will result in ¹⁸O enrichment in the HCO₃⁻ (aq) reservoir and ultimately in the precipitated CaCO₃.     

The relation between c dimension and exchange components in micas

Summary A number of micas of varying compositions and polytypism have been selected from the literature for multiple linear regression analysis. The c dimension in micas is found to depend on the sizes of the interlayer cation, d_i, and tetrahedral cation, d_t, as well as on the hydroxyl content, [OH]. The regression equation obtained: c_r = 5.415 + 0.071[OH] + 2.098d_i + 2.335d_t with R² = 90.5%, shows that the three variables affect the c-axis dimension in the order d_t > d_i [OH]. Addition of 2- and 3-layer polytypes to the regression analysis reduces R² to 87.2%. Application of the regression analysis to synthetic Al-rich biotites from the literature shows that the amount of [A1^IVA1^VI]_1Y[Fe²⁺, MgSi]_–1y in solid solution is limited and always less than [A1^VIO]_1z[Fe²⁺, MgOH]_–1z (i.e. 0.35 > y z). The maximum value of the vector y in solution is slightly higher than that reported for natural Al-rich biotites.

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Die Beziehung zwischen der Gitterkonstante c und den Austauschkomponenten in Glimmern

Zusammenfassung Eine Anzahl von Glimmern unterschiedlicher Zusammensetzung und Polytypie wurde aus der Literatur für eine multiple lineare Regressionsanalyse ausgewählt. Es stellte sich heraus, dass in Glimmern die Gitterkonstante c von den Grössen des Zwischenschicht-Kations d_i und des tetraedrischen Kations d_t abhängt, ferner vorn Hydroxylgehalt, [OH]. Die erhaltene Regressionsgleichung c_r = 5,415 + 0,071 [OH] + 2,098d_i + 2,335d_t mit R² = 90,5% zeigt, dass die drei Variablen die Grösse der c-Achse in der Reihenfolge d_t > d_i [OH] beeinflussen. Der Einschluss von 2- und 3-Schicht Polytypen in die Regressionsanalysen verkleinert R² auf 87,2%. Die Anwendung der Regressionsanalysen auf synthetische Al-reiche Biotite aus der Literatur zeigt, der Betrag von [A1^IVA1^VI]_1y[Fe²⁺, MgSi]_–1y beschränkt und immer kleiner als [A1^VIO]_1z[Fe²⁺, MgOH]_–1z (mit 0,35 < y z) ist. Der Maximalwert des Vektors y in Lösung ist etwas grösser als jener, der für natürliche Al-reiche Biotite angegeben wurde.

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