Cumulate gabbros from the Southwest Indian Ridge, 54°S-7° 16′ E: implications for magmatic processes at a slow spreading ridge

A diverse volcanic and plutonic rock suite was recovered from the center of the 80 km long ridge segment of the Southwest Indian Ridge (54°S, 7°16 E) between the Islas Orcadas and Shaka Fracture Zones. The cumulus nature of the gabbroic rocks in the suite is indicated by phase, modal and cryptic layering, igneous lamination, and low incompatible element abundances. We present a mass-balance model for calculating the proportions and compositions of cumulus phases and crystallized intercumulus liquid from bulk-rock major element compositions. The model is based on the ability to define a compositional array of basaltic liquids and on the assumption that cumulus minerals are initially in equilibrium with trapped liquid. Calculated proportions of trapped liquid range from 3%–15%; values that are characteristic of adcumulates to mesocumulates. Models of postcumulus crystallization indicate significant enrichments of incompatible elements and buffering of compatible elements in residual trapped liquids, thus explaining the high TiO₂ contents observed in magnesian clinopyroxenes. Cumulus phase assemblages and compositions suggest solidification in shallow level magma chambers, but disequilibrium plagioclase compositions suggest some crystallization at greater depth. Furthermore, basalt compositions projected onto the olivine-clinopyroxenequartz pseudoternary suggest magma generation over a range of pressures (from less than 10 to greater than 20 kb) as well as polybaric fractional crystallization. We suggest that the Southwest Indian Ridge is characterized by low magma supply with small batches of melt that either ascend directly to the surface having undergone limited polybaric crystallization or are trapped in shallow crustal magma chambers where they evolve and solidify to form cumulate gabbros. The adcumulus nature of the gabbros investigated here suggests slow cooling rates typical of large intrusions implying relatively large, but ephemeral magma chambers below segments of the Southwest Indian Ridge.     

Alkaline hybrid mafic magmas of the Yampa area,NW Colorado,and their relationship to the Yellowstone mantle plume and lithospheric mantle domains

The Yampa volcanic field (late Miocene) consists of about 70 outcrops of monogenetic cinder cones, lavas, dykes, volcanic necks and hydrovolcanic pyroclastic deposits and is situated in the most northerly part of the Rio Grande rift. Contemporaneous extension in this part of the rift was small, but there is geological and geophysical evidence that, by the late Miocene, the area was underlain by hot asthenosphere convected by the Yellowstone mantle plume. The Yampa rocks are mafic and chemically diverse, including basanites, alkali basalts, potassic trachybasalts, hawaiites and shoshonites. About half the rocks bear the xenocryst suite feldspar, pyroxene, Fe–Ti oxide, amphibole, biotite. There is a tendency for xenocryst-free rocks to be the most mafic, interpreted to indicate that the xenocrysts are cognate, and represent cumulate material from fractional crystallization of the magmas in deep crustal magma chambers. The elemental and isotopic (Nd and Sr) variations can be modelled by mixing variable proportions of partial melts of local lithospheric mantle with an OIB end-member formed by partial melting of asthenosphere. The OIB end-member appears to have the elemental and isotopic composition of typical Northern Hemisphere OIB, in particular the plume-derived basanites of Loihi seamount, Hawaii. The OIB end-member at Yampa is interpreted to have been derived from mantle convected in the Yellowstone mantle plume.     

Lake Hoare, Antarctica: sedimentation through a thick perennial ice cover

Lake Hoare in the Dry Valleys of Antarctica is covered with a perennial ice cover more than 3 m thick, yet there is a complex record of sedimentation and of growth of microbial mats on the lake bottom. Rough topography on the ice covering the lake surface traps sand that is transported by the wind. In late summer, vertical conduits form by melting and fracturing, making the ice permeable to both liquid water and gases. Cross-sections of the ice cover show that sand is able to penetrate into and apparently through it by descending through these conduits. This is the primary sedimentation mechanism in the lake. Sediment traps retrieved from the lake bottom indicate that rates of deposition can vary by large amounts over lateral scales as small as 1 m. This conclusion is supported by cores taken in a 3 × 3 grid with a spacing of 1.5 m. Despite the close spacing of the cores, the poor stratigraphic correlation that is observed indicates substantial lateral variability in sedimentation rate. Apparently, sand descends into the lake from discrete, highly localized sources in the ice that may in some cases deposit a large amount of sand into the lake in a very short time. In some locations on the lake bottom, distinctive sand mounds have been formed by this process. They are primary sedimentary structures and appear unique to the perennially ice-covered lacustrine environment. In some locations they are tens of centimetres high and gently rounded with stable slopes; in others they reach ～ 1 m in height and have a conical shape with slopes at angle of repose. A simple formation model suggests that these differences can be explained by local variations in water depth and sedimentation rate. Rapid colonization and stabilization of fresh sand surfaces by microbial mats composed of cyanobacteria, eukaryotic algae, and heterotrophic bacteria produces a complex intercalation of organic and sandy layers that are a distinctive form of modern stromatolites.     

Geochemistry of meteoric calcite cements in some Pleistocene limestones

In this study, the stable isotope and trace element geochemistries of meteoric cements in Pleistocene limestones from Enewetak Atoll (western Pacific Ocean), Cat Island (Bahamas), and Yucatan were characterized to help interpret similar cements in ancient rocks. Meteoric calcite cements have a narrow range of δ¹⁸O values and a broad range of δ¹³C values in each geographical province. These Pleistocene cements were precipitated from water with stable oxygen isotopic compositions similar to modern rainwater in each location. Enewetak calcite cements have a mean δ¹⁸O composition of ?6.5%₀ (PDB) and δ¹³C values ranging from ?9.6 to +0.4%0 (PDB). Sparry calcite cements from Cat Island have a mean δ¹⁸O composition of ?4.1%₀ and δ¹³C values ranging from ?6.3 to + 1.1%₀. Sparry cements from Yucatan have a mean δ¹⁸O composition of ?5.7%₀ and δ¹³C values of ?8.0 to ?2.7%₀. The mean δ¹⁸O values of these Pleistocene meteoric calcite cements vary by 2.4%₀ due to climatic variations not related directly to latitude. The δ¹³C compositions of meteoric cements are distinctly lower than those of the depositional sediments. Variations in δ¹³C are not simply a function of distance below an exposure surface. Meteoric phreatic cements often have δ¹³C compositions of less than —4.0%₀, which suggests that soil-derived CO₂ and organic material were washed into the water table penecontemporaneous with precipitation of phreatic cements. Concentrations of strontium and magnesium are quite variable within and between the three geographical provinces. Mean strontium concentrations for sparry calcite cements are, for Enewetak Atoll, 620 ppm (σ= 510 ppm); for Cat Island, 1200 ppm (σ= 980 ppm); and for Yucatan, 700 ppm (σ= 390 ppm). Equant cements, intraskeletal cements, and Bahamian cements have higher mean strontium concentrations than other cements. Equant and intraskeletal cements probably precipitated in more closed or stagnant aqueous environments. Bahamian depositional sediments had higher strontium concentrations which probably caused high strontium concentrations in their cements. Magnesium concentrations in Pleistocene meteoric cements are similar in samples from Enewetak Atoll (mean =1.00 mol% MgCO₃; σ= 0.60 mol% MgCO₃) and Cat Island (mean = 0.84 mol% MgCO₃; σ= 0.52mol% MgCO₃) but Yucatan samples have higher magnesium concentrations (mean = 2.20 mol% MgCO₃: σ= 0.84mol% MgCO₃). Higher magnesium concentrations in some Yucatan cements probably reflect precipitation in environments where sea water mixed with fresh water.     

Triton: stratospheric molecules and organic sediments

Hydrocarbons and nitriles are produced in Triton's stratosphere by energetic electrons from Neptune's magnetosphere and other charged particle sources. Laboratory plasma experiments reported here show a substantial yield of molecules from low pressure flows of 10(-3) CH4 in N2 appropriate to Triton if both CH4 and N2 are saturated at the surface. An active magnetosphere similar to that of Uranus would result in a flux approximately 0.3 erg cm-2 s-1 of 0.1-1 MeV electrons in Triton's stratosphere; molecular production rates are then 10(6)-10(8) cm-2 s-1 for NH3, C2H2, HCN, and NCCN; tens of hundreds of gm cm-2 of these compounds per 10(9) yr (and lesser quantities of at least eight other molecules experimentally detected) would freeze to fine-grained white condensates in the lower stratosphere and sediment to the surface. Along with dark/colored organic haze produced in the stratosphere and other heteropolymers produced at the surface, these condensates are subjects to redistribution by aeolian processes and may appear as lag deposits and/or sediment layers. A simple eddy diffusion model indicates abundances approximately 10(19) molec cm-2 for HCN and C2H2, and > 10(17) molec cm-2 for NCCN, CH3CCH, CH2CCH2, and CH3CN in the stratosphere; these and other organic molecules will be detectable by IRIS if the stratosphere is (as expected) heated through ultraviolet and visible light absorption by the haze.     

Geomagnetic evolution: 400 years of change on planet Earth

Spherical harmonic coefficients of the geomagnetic field, calculated from historical observations of declination, inclination and intensity, and from archaeomagnetic inclination results, have been used to produce a film of geomagnetic change since 1600 A.D. The non-dipole geomagnetic field is found to be constantly changing: no fixed or standing non-dipole features are observed. Non-dipole foci are seen to have lifetimes of a few hundred years. The westward drift, which was an important feature of the 18th and early 19th century geomagnetic field, was less pronounced in the 17th century. The growth, evolution, decay and replacement of non-dipole foci, but not their movement are found to have been the major features producing century-long secular directional magnetic variation. Most of the low degree and order spherical harmonic coefficients have changed significantly over the last few hundred years. In particular the change in sign of the axisymmetric quadrupole around 1837 A.D. is noted. Sustained, century-long, intensity changes, however, appear to have been dominated by variations in the intensity of the centred dipole, rather than by non-dipole field fluctuations.     

Arsenic and antimony in geothermal waters of Yellowstone National Park,Wyoming, USA

A total of 268 thermal spring samples were analyzed for total soluble As using reduced molybdenum-blue; 27 of these samples were also analyzed for total Sb using flame atomic absorption spectrometry. At Yellowstone the $\text{Cl}\text{As}$ atomic ratio is nearly constant among neutral-alkaline springs with Cl > 100 mg L^?1, and within restricted geographic areas, indicating no differential effects of adiabatic vs. conductive cooling on arsenic. The $\text{Cl}\text{As}$ ratio increases with silica and decreases with decreasing $\text{Cl}\text{ΣCO}{}_3$; the latter relationship is best exemplified for springs along the extensively sampled SE-NW trend within the Lone Star-Upper-Midway Basin region. The relationship between $\text{Cl}\text{As}$ and $\text{Cl}\text{ΣCO}{}_3$ at Yellowstone suggests a possible rock leaching rather than magmatic origin for much of the Park's total As flux. Condensed vapor springs are low in both As and Cl. Very high $\text{Cl}\text{As}$ ratios ( > 1000) are associated exclusively with highly diluted (Cl < 100 mg L^?1) mixed springs in the Norris and Shoshone Basins and in the Upper White Creek and Firehole Lake areas of Lower Basin. The high ratios are associated with acidity and/or oxygen and iron; they indicate precipitation of As following massive dilution of the Asbearing high-Cl parent water.Yellowstone Sb ranged from 0.009 at Mammoth to 0.166 mg L^?1 at Joseph's Coat Spring. Within basins, the $\text{Cl}\text{Sb}$ ratio increases as the $\text{Cl}\text{ΣCO}{}_3$ ratio decreases, in marked contrast to As. Mixed springs also have elevated $\text{Cl}\text{Sb}$ ratios. White (1967) and Weissberg (1969) previously reported stibnite (Sb₂S₃), but not orpiment (As₂S₃), precipitating in the near surface zone of alkaline geothermal systems.     

Petrogenesis of the Kinsman Intrusive Suite: Peraluminous Granitoids of Western New Hampshire

The Kinsman Intrusive Suite occurs in six major plutons of westernNew Hampshire, covering a total area of 2240 km². It is an Acadian-agesyntectonic gneissic S-type peraluminous granitoid, rangingin composition from quartz diorite to granite. Much of the Kinsmanis characterized by very large (up to 120 mm in maximum dimension)megacrysts of alkali feldspar, but the bulk chemistry of therocks indicates that these cannot be phenocrysts crystallizedfrom initially homogeneous melts. Locally, there is abundant(20 per cent) almandine-rich garnet, and graphite is a commonaccessory.In contrast to the unannealed orthoclase in surroundingmetapelites, the alkali feldspar of the Kinsman has, for themost part, inverted to maximum microcline. The garnets havecore temperatures in the range of 800 to 900 ?C, and are pseudomorphedby, or show reaction rims to, biotite. Plagioclase commonlyshows zoning, some of it oscillatory. These features are magmaticin nature, and argue against the conclusions of previous investigatorsthat the mineralogy and textures of the rock are due to regionalmetamorphism of a previously-crystallized two-mica granitoidwhich has undergone prograde reactions such as:muse + bio +3 qtz 2 Kfs + gar + 2H₂O.The intrusives have also producedrecognizable contact-metamorphic features in the wallrocks andare probably coeval with the dominant M2 Acadian metamorphism.Majorelement analytical data for the Kinsman suite has been examinedby least squares mixing-model and extended Q-mode factor analysis.These calculations, supported by consideration of REE data,suggest that the most likely origin for the Kinsman magmas isby deep-crustal anatexis of slightly calcareous metapelites,and involves a reaction such as:bio + Al₂SiO₅ + qtz + feldspars gar + cord + Kfs + plag + melt.In non-calcareous pelites thisreaction produces a water-undersaturated peraluminous melt attemperatures above 700 ?C, and allows for the early crystallizationor recrystallization of K-feldspar, plagioclase, and garnetin a crystal-liquid mush or migma. Geochemically, garnet + plagioclaseare treated as restite, and a minimum-melt granite as the magmain the Q-mode and mixing-model calculations. The variabilityin chemistry of the Kinsman Intrusive Suite is best explainedon the basis of mixing of leucogranitic anatectic melts withgarnet-plagioclase restitic material and a quartz-feldspar-sillimanite-biotiterock, but only very slightly affected by crystal settling.