Variations in andean andesite compositions and their petrogenetic significance

Three linear zones of active andesite volcanism are present in the Andes — a northern zone (5°N–2°S) in Colombia and Ecuador, a central zone (16°S–28°S) largely in south Peru and north Chile and a southern zone (33°S–52°S) largely in south Chile. The northern zone is characterized by basaltic andesites, the central zone by andesite—dacite lavas and ignimbrites and the southern zone by high-alumina basalts, basaltic andesites and andesites. Shoshonites and volcanic rocks of the alkali basalt—trachyte association occur at scattered localities east of the active volcanic chain,The northern and central volcanic zones are 140 km above an eastward-dipping Benioff zone, while the southern zone lies only 90 km above a Benioff zone. Continental crust is ca. 70 km in thickness below the central zone, but is 30–45 km thick below northern and southern volcanic zones. The correlation between volcanic products and their structural setting is supported by trace element and isotope data. The central zone andesite lavas have higher Si, K, Rb, Sr and Ba, and higher initial Sr isotope ratios than the northern or southern zone lavas. The southern zone high-alumina basalts have lower Ce/Yb ratios than volcanics from the other zones. In addition, the central zone andesite lavas show a well-defined eastward increase in K, Rb and Ba and a decrease in Sr.Andean andesite magmas are a result of a complex interplay of partial melting, fractional crystallization and “contamination” processes at mantle depths, and contamination and fractional crystallization in the crust. Variations in andesite composition across the central Andean chain reflect a diminishing degree of partial melting or an increase in fractional crystallization or an increase in “contamination” passing eastwards. Variations along the Andean chain indicate a significant crustal contribution for andesites in the central zone, and indicate that the high-alumina basalts and basaltic andesites of the southern zone are from a shallower mantle source region than other volcanic rocks. The dacite-rhyolite ignimbrites of the central zone share a common source with the andesites and might result from fractional crystallization of andesite magma during uprise through thick continental crust. The occurrence of shoshonites and alkali basalts eat of the active volcanic chain is attributed to partial melting of mantle peridotite distant from the subduction zone.     

A proposed model for predicting trace metal composition of fly-ash leachates

A mathematical model is proposed that is designed to predict trace metal composition of leachates produced by coal fly ashes. This model is based on the assumption that the mobilization of trace metals from fly ash is primarily a surface desorption phenomenon. The validity of this model is tested using data from published sources. Good correlation is found between predicted trace metal concentrations and measured trace metal concentrations in experimentally produced leachates.     

Note on the genesis of brucite in contact metamorphism of dolomite

Consideration of available thermodynamic data and the published results of direct experiments relating to (1) formation. of periclase from dolomite and (2) hydration of periclase to brucite, permits the following conclusions to be drawn: (1) At very low partial pressures of CO₂ (perhaps of the order of 1 bar) and relatively high partial pressures of water (up to 2000 bars), dolomite can break down directly to brucite and calcite at temperatures above about 400° C, and below temperatures on the brucite dehydration curve. (2) The reaction dolomite calcite + periclase + CO₂ in contact metamorphism near granitic bodies is likely to occur only at low partial pressures of CO₂ (perhaps 10 or 20 bars); this can be achieved without direct formation of brucite, by maintaining a partial pressure of water of the order of 1000 bars or more. (3) At low CO₂ pressures dolomite may re-form in the cooling stages of metamorphism by reaction between calcite, brucite, and CO₂ at temperatures below about 400° C.     

Crystal bending in metamorphic calcite,and its relations to associated twinning

This paper deals with the incidence and geometry of lattice bending in calcite of naturally strained marble and possible relations in time to associated {01¯12} twinning, as revealed by microscopic examination with a universal stage. Microscopic technique and graphic treatment of data with a view to identifying the relation in time of bending to twinning, and possible glide mechanisms involved in the bending process are reviewed as a basis for present and subsequent investigation of this general topic.In most instances development of surviving thin e twins postdates bending of the host crystal (such twins everywhere are rationally oriented). Rarely (in contrast with experimental experience) some thin twins are slightly irrational (L_e lamellae) and apparently developed in the final stages of bending. Thick twins (a few tens of microns wide) on the other hand rather commonly predate or are synchronous with bending.The geometry of bending (external rotation) — especially for rotation less than 25° —commonly is compatible with models (based on experimental experience) of simple translation in the strained domains. The commonest translation system so identified is on {10¯11}, with sense of shear, where recognizable, either negative or positive. Translation on {02¯21} is relatively rare. Unexpectedly there is rather strong but not conclusive evidence of translation on {0001} parallel to an a axis. This mechanism, hitherto never identified with certainty, is now here documented unequivocally in a crystal of calcite experimentally strained at 300° C, 5 kb.     

Amphibole pyroxenite xenoliths: Cumulate or replacement phenomena from the upper mantle,Nunivak Island,Alaska

Interstitial to poikilitic amphibole found in garnet pyroxenite xenoliths has been interpreted, in the past, to represent a critically silica undersaturated, residual intercumulus melt trapped by its cumulate assemblage of anhydrous phases. The textural features of such amphibole in pyroxenite xenoliths from Nunivak Island, Alaska, however, are more compatible with an origin by replacement of the anhydrous phases of the pyroxenite, following a period of cooling and sub-solidus recrystallization in the upper mantle. The reaction of amphibole and olivine to give orthopyroxene, observed in two specimens, requires that the associated fluid phase was not critically silica undersaturated. The amphibole is therefore thought to reflect the interaction of an alkali-bearing, migratory, aqueous fluid and an upper mantle consisting of spinel lherzolite cut by veins of spinel and garnet pyroxenite.     

Some trace element relationships among liquid and solid phases in the course of the fractional crystallization of magmas

The classical equations relating the trace element concentrations of the liquid and solid phases coexisting in the simple fractional crystallization of a parental magma have been put in a simple graphical form, which allows rapid analysis of the possible genetic relationships in a given rock suite. The effects of an incomplete separation between the two phases are taken into account. The approach does not require the use of otherwise estimated partition coefficients. Trace element data concerning the minerals of cumulates, where available, may provide an independent estimation of the effective mineral-liquid partition coefficients. With reasonable assumptions, this approach may even be applied to plutonic rocks. Interpretation of the published rare earth element data from the Southern California Batholith by this procedure suggests that a tonalitic parental magma could generate a granodioritic liquid by crystallizing 40–50 wt % of a solid residue of gabbroic composition, in agreement with Larsen's (Mem. Geol. Soc. Amer. 29, 1948) calculations. The calculated mineral-liquid partition coefficients for the REE fall in the range of published phenocryst-groundmass values for acidic volcanic rocks.     

Mercury surface composition: Integrating petrologic modeling and remote sensing data to place constraints on FeO abundance

A significant opaque component in Mercury’s crust is inferred based on albedo and spectral observations. Previous workers have favored iron-titanium bearing oxide minerals as the spectrally neutral opaque. A consequence of this hypothesis is that Mercury’s surface would have a high FeO content. An array of remote sensing techniques have not provided definitive constraints on the FeO content of Mercury’s surface. However, spectral observations have not detected a diagnostic 1 μm absorption band and have thus limited the FeO in coexisting silicates to <2 wt.% FeO. In this paper, we assess equilibrium among oxide and silicate minerals to constrain the distribution of iron between opaque oxides and silicates under a variety of environmental conditions. Equilibrium modeling is favored here because the geologic process that produced Mercury’s low-albedo intermediate terrain must have occurred globally, which favors a common widespread igneous process. Based on our modeling, we find that iron-rich ilmenite cannot occur with silicates that do not display a 1 μm absorption feature unless plagioclase abundances are high. However, such high plagioclase abundances are precluded by Mercury’s low albedo. Incorporating equilibrium crystallization modeling with spectral and albedo constraints we find the iron abundance of Mercury’s intermediate terrain is ?10 wt.% FeO. This intermediate iron composition matches constraints provided by visible albedo and total neutron absorption observed by MESSENGER. In fact, the total neutron absorption of mixtures of oxide, plagioclase, olivine and pyroxene for the oxide abundances estimated for Mercury, favor Mg-rich members of the ilmenite-geikielite solid-solution series. This work offers compositional constraints for Fe, Ti, and Mg that will be testable by various MESSENGER instrument data sets after it begins its orbital mission.     

Letters to the editor

A preliminary scuba survey of oligotrophic Lake Rotoma in 1972 revealed a vegetation mainly composed of native hydrophytes in which exotics were at an early stage of colonisation. In 1973 the presence of species was recorded in 5708 quadrats (625 cm²) at 1 m intervals along a total of 50 line transects placed systematically around the lake. Water depth was measured, and quadrat cover and substrate type were subjectively estimated. Species frequency calculations showed that the dominant vegetation pattern was a characean meadow of Chara fibrosa f. acanthopitys (A.Br.) R.D.W., Nitella leptostachys var. leonhardii (R.D.W.) R.D.W., and N. pseudoflabellata var. mucosa (Nordst.) Bailey. The charophytes extended over a depth range of 1–17.5 m on a wide variety of substrates and gradients. Native vascular plants were absent from many transects, and had a depth range only from 0 to 4.5 m, with most occurring above 3.5 m. The Low Mixed Community, found in shallow water less than 1.25 m in depth at the northeast end of the lake, provided this area with a high species diversity. Exotic hydrophytes had established in many areas around the lake. The distribution of Lagarosiphon major (Ridley) Moss and Elodea canadensis Michx. appeared to coincide with boating access and fallen submerged trees over a depth range of 0–6.0 m, although much of the available habitat had not yet been exploited. Emergent species were most abundant within the southwest inlet and also in the lagoons surrounding the lake where sheltered conditions and shallow gradients prevail.     

Genetic variation and population structure in the New Zealand snapper

Fifteen proteins encoded by 23 gene loci were electrophoretically surveyed in two samples of snapper Chrysophrys auratus (Forster) from Wellington Harbour and the Hauraki Gulf. Between 17% and 26% of the loci examined were found to be polymorphic and the proportion of heterozygous loci per individual was 7.9% to 8.4%. Using Rogers’ genetic distance coefficient an overall similarity of 0.98 was calculated between the two samples.

Three polymorphic loci Est‐4, Gpi‐1, and Idh were examined in an additional 10 samples from around New Zealand. Two genetically distinct stocks were apparent: one along the west coast, the other along the east coast of the North Island. There was an indication of stock mixing at Ninety Mile Beach and in the Bay of Plenty and East Cape. The distribution of alleles at the Est‐4 locus revealed a third stock in Hawke Bay that is genetically more similar to the west coast than the east coast stock. Hydrological conditions in Hawke Bay are more similar to those of the west coast than to those of the north east coast of the North Island. Thus it is possible that Est‐4 alleles are selectively maintained in response to an environmental factor.