Amelioration of soil fertility by woody perennials in cropping fields: evaluation of three tree species in the semi-arid zone of Nigeria

Soil was sampled from cropping fields in radial patterns from beneathAcacia albida, Parkia bigloboza(Jacq.) Benth. andEucalyptus camaldulensisDehnh. near Zaria, Nigeria. Results of analysis show a significant coarsening of soil texture and a decrease in organic matter and cation exchange capacity with increasing distance from all three tree species at a depth of 0–15 cm. Concentrations of nitrogen and some exchangeable cations decreased significantly with increasing distance from beneath acacia and parkia, and soil pH decreased with increasing distance from eucalyptus. The implication of the results for land management are discussed in relation to increasing productivity and soil use sustainability.     

Fluid inclusion evidence for the physicochemical conditions of sulfide deposition in the Olympias carbonate-hosted Pb-Zn(Au, Ag) sulfide ore deposit, E. Chalkidiki peninsula, N. Greece

The Olympias Pb-Zn(Au, Ag) sulfide ore deposit, E. Chalkidiki, N. Greece, is hosted by marbles of the polymetamorphic Kerdilia Formation of Paleozoic or older age. The geologic environment of the ore also comprises biotite-hornblende gneisses and amphibolites intruded by Tertiary pegmatite-aplite dikes, lamprophyre dikes, the 30-Ma Stratoni granodiorite, and porphyritic stocks. Only limited parts of the deposit display shear folding and brecciation; most of it is undeformed. Microthermometry of fluid inclusions in gangue syn-ore quartz indicates three types of primary and pseudosecondary inclusions: (1) H₂O-rich, 1–18 wt.% NaCl equivalent, <3.6 mol% CO₂; (2) H₂O-CO₂ inclusions, <4wt.% NaCl equivalent, with variable CO₂ contents, coexisting in both undeformed and deformed ore; (3) aqueous, highsalinity (28–32 wt,% NaCl equivalent) inclusions found only in undeformed ore. Type 2 inclusions are differentiated into two sub-types: (2a) relatively constant CO₂ content in the narrow range of 8–15 mol% and homogenization to the liquid phase; (2b) variable CO₂ content between 18 and 50 mol% and homogenization to the vapor phase. Type 1 and 2b inclusions are consistent with trapping of two fluids by unmixing of a high-temperature, saline, aqueous, CO₂-bearing fluid of possible magmatic origin, probably trapped in type 2a inclusions. Fluid unmixing and concomitant ore mineralization took place at temperatures of 350 ± 30 °C and fluctuating pressures of less than 500 bar, for both undeformed and deformed ores. The wide salinity range of type 1 inclusions probably represents a complex effect of salinity increase, due to fluid unmixing and volatile loss, and dilution, due to mixing with low-salinity meteoric waters. High solute enrichment of the residual liquid, due to extreme volatile loss during unmixing, may account for high salinity type 3 inclusions. The Olympias fluid inclusion salinity-temperature gradients bear similarities to analogous gradients related to Pb-Zn ores formed in “granite”-hosted, low-T distalskarn, skarn-free carbonate-replacement and epithermal environments.     

Composition of hydrous melts in equilibrium with quartz eclogites

Summary Compositions of the hydrous melts in equilibrium with garnet, omphacitic clinopyroxene and quartz have been investigated experimentally at 28.5 and 35 kbar. They are represented by silica-rich liquids (> 70% SiO₂) with low MgO, FeO and CaO contents. The removal of ca 10–15% of the magma of this composition may be sufficient to convert quartz eclogite formed after subduction of altered MORB into a quartz-free bimineralic eclogite assemblage, which is a common type of xenoliths in kimberlites.At 28.5 kbar the solidus temperature is between 700 and 750° C in the system quartz eclogite—water, and the high pressure amphibole-out boundary lies at ca 25 kbar in accord with the previous studies.

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Die Zusammensetzung wasserhältiger Schmelzen im Gleichgewicht mit Quarz-Eklogiten

Zusammenfassung Um Prozesse zu simulieren, die bei der Subduktion von Ozeanbodenbasalten durch partielle Anatexis im Stabilitätsfeld von Eklogiten ablaufen, wurde die Zusammensetzung wasserhältiger Schmelzen in Gleichgewicht mit Granat, Omphacit und Quarz bei 28.5 und 35 Kbar experimentell untersucht. Diese Schmelzen sind reich an SiO₂ (> 70 Gew%) und arm an Mg0, Fe0 and CaO. Die Extraktion von ca. 10–15% derartiger Schmelzen würde genügen, um quarzführende Eklogite, die durch die Subduktion von alteriertem MORB Material entstanden sind, in quarzfreie bimineralische Eklogite umzuwandeln wie sie häufig als Xenolithe in Kimberliten beobachtet werden.Im System Quarz-Eklogit-Wasser liegt die Solidustemperatur bei 28.5 Kbar zwischen 700 und 750°C. Die obere Stabilitätsgrenze von Amphibol liegt in diesem Temperaturbereich bei ca. 25 Kbar.

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With 1 Figures     

Using Hydrogeochemical Methods To Evaluate Complex Quaternary Subsurface Stratigraphy Block Island,Rhode Island,USA

One of the major problems in hydrogeologic investigations of glaciated regions is the determination of complex stratigraphic relationships in the subsurface where insufficient information is available from drilling and geophysical records. In this paper, chemical characteristics of groundwater were used to identify stratigraphic changes in glacial deposits that were previously inferred on Block Island, Rhode Island, USA, an emergent remnant of the late Wisconsinan terminal moraine, located approximately 16 km south of the Rhode Island mainland. Two chemically distinct water types are recognized on the island: 1) high-iron, characterized by dissolved silica levels in excess of 20 mg/L, bicarbonate greater than 30 mg/L and dissolved iron ranging from 1-20 mg/L; and 2) low-iron, characterized by dissolved silica levels below 16 mg/L, bicarbonate less than 30 mg/L, and less than 0.3 mg/L dissolved iron. The spatial distribution of iron-bearing minerals and organic matter and the resulting redox conditions are believed to control the occurrence of high-iron groundwater. The high-iron waters occur almost exclusively in the eastern half of the island and appear to coincidence with the presence of allochthonous blocks of Cretaceous-age coastal-plain sediments that were incorporated into Pleistocene-age deposits derived from the Narragansett Bay-Buzzard's Bay lobe of the Late Wisconsinan Laurentide ice sheet. The low-iron waters occur in the western half of the island, where the occurrence of these Cretaceous-age blocks is rare and the sediments are attributed to a sublobe of the Hudson-Champlain lobe of the Late Wisconsinan ice-sheet. RÉSUMÉ: L'un des principaux problèmes dans les études hydrogeologiques des régions qui ont été englacées est la définition des relations stratigraphiques complexes sous la surface, lá où les informations fournies par les forages et par la géophysique sont insuffisantes. Dans l'exemple traité, les caractéristiques chimiques de l'eau souterraine sont utilisées pour identifier les variations stratigraphiques dans les dépôts glaciaires qui avaient auparavant été supposées, sur l'île de Block (Rhode Island), restes émergeant d'une moraine terminale du Wisconsinien récent, situé à environ 16 km au sud de Rhode Island. Deux types d'eau chimiquement distincts ont été reconnus dans l'île: 1) à fortes teneurs en fer, caractérisées par des concentrations en silice supérieures à 20 mg/L, en bicarbonates supérieures à 30 mg/L et en fer comprises entre 1 et 20 mg/L; et 2) à faibles teneurs en fer, marquées par des concentrations en silice inférieures à 16 mg/L, en bicarbonate inférieures à 30 mg/L et en fer dissous inférieures à 0.3 mg/L. La distribution spatiale des minéraux riches en fer et de la matière organique et les conditions redox résultantes contrôlent probablement la présence de fer dans les eaux souterraines à fortes concentrations. Les eaux à fortes teneurs en fer sont connues presque exclusivement dans la moitié orientale de l'île et semblent coïncider avec la présence de blocs allochtones provenant des sédiments côtiers crétacés, introduits dans les formations pléistocènes liées au lobe glaciaire des baies de Narragansett et du Busard de la calotte glaciaire laurentide du Wisconsinien récent. Les eaux à faibles teneurs en fer apparaissent dans la moitié occidentale de l'île, là où ces blocs de Crétacé sont rares et où les sédiments sont attrbués à une digitation du lobe de l'Hudson-Champlain de la calotte glaciaire du Wisconsinien récent. RESUMEN: Uno de los mayores problemas en la investigación hidrogeológica en regiones glaciares es la determinación de las complejas relaciones estratigráficas en el subsuelo, donde la información procedente de registros de perforaciones y de geofísica no es suficiente. En este artículo, se han usado las características químicas del agua subterránea para identificar unos cambios estratigráficos que se habían predicho previamente en unos depósitos glaciares en Block Island, Rhode Island (Estados Unidos), un remanente emergente de la morrena terminal del Winsconsiniense tardío, situada unos 16 km al sur de la Rhode Island continental. En la isla se encuentran dos tipos de agua distintos: 1) de alto contenido en hierro, caracterizada por niveles de sílice disuelto superando los 20 mg/L, bicarbonatos por encima de 30 mg/L y hierro disuelto oscilando entre 1-20 mg/L; y 2) de bajo contenido en hierro, caracterizada por niveles de sílice disuelto inferiores a 16 mg/L, bicarbonatos por debajo de 30 mg/L y menos de 0.3 mg/L de hierro disuelto. La distribución espacial de los minerales ricos en hierro y de la materia orgánica, así como las condiciones redox resultantes se supone que condicionan la presencia de aguas de alto contenido en hierro. Estas aguas aparecen casi exclusivamente en la mitad oriental de la isla y parecen coincidir con la presencia de bloques alóctonos de sedimentos costeros, de edad cretácica, que se incorporaron a los depósitos de edad pleistocena procedentes del lóbulo de la Bahía de Narragansett-Bahía de Buzzard, correspondiente a la capa glaciar del Winsconsiniense-Lauréntido tardío. Las aguas de bajo contenido en hierro aparecen en la mitad occidental de la isla, donde la presencia de estos sedimentos de edad cretácica es rara y los sedimentos se suponen procedentes de un sublóbulo del lóbulo de Hudson-Camplain, correspondiente a la capa glaciar del Winsconsiniense tardío.     

Melting of albite and dehydration of brucite in H2O–NaCl fluids to 9 kbars and 700–900°C: implications for partial melting and water activities during high pressure metamorphism

 The melting reaction: albite_(solid)+ H₂O_(fluid) =albite-H₂O_(melt) has been determined in the presence of H₂O–NaCl fluids at 5 and 9.2 kbar, and results compared with those obtained in presence of H₂O–CO₂ fluids. To a good approximation, albite melts congruently at 9 kbar, indicating that the melting temperature at constant pressure is principally determined by water activity. At 5 kbar, the temperature (T)- mole fraction (X _(H2O) ) melting relations in the two systems are almost coincident. By contrast, H₂O–NaCl mixing at 9 kbar is quite non-ideal; albite melts ∼70 ^°C higher in H₂O–NaCl brines than in H₂O–CO₂ fluids for X _(H2O) =0.8 and ∼100 ^°C higher for X _(H2O) =0.5. The melting temperature of albite in H₂O–NaCl fluids of X _(H2O)=0.8 is ∼100 ^°C higher than in pure water. The P–T curves for albite melting at constant H₂O–NaCl show a temperature minimum at about 5 kbar. Water activities in H₂O–NaCl fluids calculated from these results, from new experimental data on the dehydration of brucite in presence of H₂O–NaCl fluid at 9 kbar, and from previously published experimental data, indicate a large decrease with increasing fluid pressure at pressures up to 10 kbar. Aqueous brines with dissolved chloride salt contents comparable to those of real crustal fluids provide a mechanism for reducing water activities, buffering and limiting crustal melting, and generating anhydrous mineral assemblages during deep crustal metamorphism in the granulite facies and in subduction-related metamorphism. Low water activity in high pressure-temperature metamorphic mineral assemblages is not necessarily a criterion of fluid absence or melting, but may be due to the presence of low a _(H2O) brines. Received: 17 March 1995/Accepted: 9 April 1996     

Magma dynamics at the base of an evolving mafic magma chamber: Incompatible element evidence from the Partridge River intrusion, Duluth Complex, Minnesota, USA

A characteristic feature of the Partridge River intrusion of the Keweenawan Duluth Complex is the approximately fivefold to ninefold increase in the concentrations of incompatible elements in the lower zone compared with cumulates stratigraphically higher. The concentrations of incompatible elements decrease from the lower zone upward to steady state values, which is ascribed to variations in the proportions of trapped liquid rather than variable degrees of fractional crystallization of a single parental magma. The calculated average composition of trapped liquid using our algorithm is similar to typical Keweenawan low-alumina, high Ti---P basalts associated with the Duluth Complex but is different from the leading edge ferrodioritic liquid quenched in the chilled margin of the intrusion. This difference suggests that the chilled margin does not represent the original (parental) magma composition from which the whole intrusion solidified, and that the enrichment of incompatible elements may be related to the local flotation of magmatic suspensions. To test the latter hypothesis numerically, we have used heat-mass transfer models, assuming a sheet-like magma chamber, to calculate the parameters of the model that best reproduce the observed distribution of incompatible elements in a mush zone at the base of the Partridge River intrusion. The results indicate that a mush zone enriched in the incompatible elements is produced if the velocity of movement of the lower solidification front into the magma body was less than the floating velocity of the bulk crystal mush. The dynamic parameters that best reproduce the observed distribution of incompatible elements include a magma emplacement pressure of 2 kbar, critical crystallinities of 50–68% in the mush zone from which the liquid is being expelled, and an emplacement temperature of 1160°C for the initial magma.     

Quaternary minettes and associated volcanic rocks of Mascota,western Mexico: a consequence of plate extension above a subduction modified mantle wedge

 Pleistocene-Holocene volcanism in the Jalisco block of western Mexico is confined to two conspicuous grabens, where potassic eruptives range from absarokites (48–52% SiO₂) and minettes (49–54% SiO₂) through basaltic andesites (53–57% SiO₂), the most voluminous type, to andesites and their lamprophyric equivalent spessartite (58–62% SiO₂); there are no contemporary rhyolitic rocks. This suite has high concentrations of Mg, Cr (<550 ppm) and Ni (<450 ppm) accompanied by large concentrations of K, P, Ba (<4000 ppm) and Sr (<5000 ppm) and elements such as LREE and Zr (<600 ppm). No combination of crystal fractionation and/or crustal contamination can reproduce the compositional range of these magmas, which nevertheless are believed to be genetically related because of their proximity in time and space. Hydrous minerals in the lamprophyres and the typical absence of plagioclase phenocrysts in both basaltic andesites and andesites reflect the relatively high concentrations of water in the magmas, which suppressed the crystallisation of feldspar. Experimental verification of the minimal amounts of water required to reproduce the phenocryst assemblages in selected rocks range from 3.5 to 6%. During ascent in a volcanic conduit, andesitic magma may lose water and consequently precipitate plagioclase, or it may ascend more rapidly, retaining more of its initial water, which stabilises phenocrysts of hornblende at the expense of plagioclase. Our estimates of water concentrations, which are consistent with the various low pressure phenocryst assemblages, will be minimal for the magmas in their source regions, and the process of magmatic dewatering on ascent may be typical in well established volcanic conduits. In accord with the compositions of phenocrystic olivine in the basaltic andesites and the minettes, the values of FeO and Fe₂O₃ of the bulk lavas and scoriae are demonstrably pristine. As a consequence, there are two characteristic features of the Mascota suite: the high range of relative oxygen fugacities (ΔNNO=1–5) and the high Mg# (MgO/MgO+FeO) that ranges from 0.70 to 0.91 (with only one andesite as low as 0.66). From the evidence of phlogopite phenocrysts, a partial melt involving phlogopite would have a higher Mg# than one from olivine (Fo₉₀) and pyroxene alone. As the Mascota series shows a correlation between K₂O and Mg#, we conclude that it was generated by partial fusion of the mantle wedge, with a variable contribution of phlogopite and apatite from veins throughout the lherzolitic assemblage. In conformity with an origin by varying increments of partial fusion of a phlogopite-bearing mantle, all incompatible elements vary linearly with Ti (or K) as if phlogopite (+apatite) in the source dominated their contribution to the partial melts. Fluids from dehydration of the subducting slab presumably deposit hydrous and other minerals in veins in the mantle wedge and also increase its redox state. As the Mascota volcanism occurs in grabens closer to the trench than the main andesite arc, it is concluded that the eruption of these small volumes of hydrous magmas require the tectonically favored ascent paths offered by the extensional grabens to reach the surface from their mantle sources. Received: 24 January 1995 / Accepted: 21 February 1996     

Contrasting stable isotope behavior between calcite and dolomite marbles,Lone Mountain,Nevada

 Late Proterozoic to Cambrian carbonate rocks from Lone Mountain, west central Nevada, record multiple post-depositional events including: (1) diagenesis, (2) Mesozoic regional metamorphism, (3) Late Cretaceous contact metamorphism, related to the emplacement of the Lone Mountain granitic pluton and (4) Tertiary hydrothermal alteration associated with extension, uplift and intrusion of silicic porphyry and lamprophyre dikes. Essentially pure calcite and dolomite marbles have stable isotopic compositions that can be divided into two groups, one with positive δ¹³C values from+3.1 to +1.4 ‰ (PDB) and high δ¹⁸O values from +21.5 to +15.8 ‰ (SMOW), and the other with negative δ¹³C values from –3.3 to –3.6‰ and low δ¹⁸O values from +16.9 to +11.1‰. Marbles also contain minor amounts of quartz, muscovite and phlogopite. Brown and blue luminescent, clear, smooth textured quartz grains from orange luminescent calcite marbles have high δ¹⁸O values from +23.9 to +18.1‰, while brown luminescent, opaque, rough textured quartz grains from red luminescent dolomite marbles typically have low δ¹⁸O values from +2.0 to +9.3‰. The δ¹⁸O values of muscovite and phlogopite from marbles are typical of micas in metamorphic rocks, with values between +10.4 and +14.4‰, whereas mica δD values are very depleted, varying from −102 to −156‰. No significant lowering of the δ¹⁸O values of Lone Mountain carbonates is inferred to have occurred during metamorphism as a result of devolatilization reactions because of the essentially pure nature of the marbles. Bright luminescence along the edges of fractures, quartz cements and quartz overgrowths in dolomite marbles, low δD values of micas, negative δ¹³C values and low δ¹⁸O values of calcite and dolomite, and depleted δ¹⁸O values of quartz from dolomite marbles all indicate that meteoric fluids interacted with Lone Mountain marbles during the Tertiary. Partial oxygen isotopic exchange between calcite and low ¹⁸O meteoric fluids lowered the δ¹⁸O values of calcite, resulting in uniform quartz-calcite fractionations that define an apparent pseudoisotherm. These quartz-calcite fractionations significantly underestimate both the temperature of metamorphism and the temperature of post-metamorphic alteration. Partial oxygen isotopic exchange between quartz and meteoric fluids also resulted in ¹⁸O depletion of quartz from dolomite marbles. This partial exchange was facilitated by an increase in the surface area of the quartz as a result of its dissolution by meteoric fluids. The negative δ¹³C values in carbonates result from the oxidation of organic material by meteoric fluids following metamorphism. Stable isotopic data from Lone Mountain marbles are consistent with the extensive circulation of meteoric hydrothermal fluids throughout western Nevada in Tertiary time. Received: 1 February 1994/Accepted: 12 September 1995     

Current controlled sediment deposition from the shelf to the deep ocean: the cenozoic evolution of circulation through the SW pacific gateway

 The circulation of cold, deep water is one of the controlling factors of the Earth's climate. Forty percent of this water enters the world ocean through the Southwest Pacific as a deep western boundary current (DWBC) flowing northwards at bathyal to abyssal depths, east of the New Zealand microcontinent. South of latitude 50°S, the DWBC is intimately linked with the Antarctic circumpolar current (ACC), which is the prominent force for the shallow-water circulation. The Pacific DWBC is presently the largest single contributor of deep ocean water, and deciphering its evolution is of fundamental importance to understanding ocean and climate history, and global ocean hydrography. The evolution of the DWBC system, and of related circum-Antarctic currents, has taken place since 30–25 Ma when plate movements created the first oceanic gaps south of Australia and South America. The stratigraphic record preserved in sediment drifts of the Southwest Pacific, in eastern New Zealand, is the best available for deciphering the Neogene history of Southern Ocean water masses, and of the circulation of the ACC, DWBC and their precursor systems. Major current activity commenced on the New Zealand margin in the late Eocene or early Oligocene (Hoiho Drift; early ACC) and was widespread by the mid-late Oligocene (Marshall Paraconformity and Weka Pass Limestone drift; ACC). During the Neogene the eastern South Island continental shelf built seawards by accretion at its outer edge of large Miocene current drifts up to tens of kilometres long and hundreds of metres thick (Canterbury drifts). Also commencing in the mid-Cenozoic, but in depths >2000 m, the DWBC emplaced large deep-water sediment drifts. Rates of drift deposition accelerated considerably in the late Neogene, when climatic change (and particularly glacial sea-level falls) caused the delivery of large volumes of turbiditic sediment into the path of the DWBC via the Bounty and Hikurangi channels. Received: 9 August 1995 / Accepted: 15 January 1996