A progress report on the design of the 8 m aperture Optical/Infrared Telescope

Progress of the design study carried out y the Instituto de Astrophysica de Canarias and Royal Greenwich Observatory joint project office for an 8 m aperture Optical/Infrared Telescope. This includes the development of an active pneumatic support system for both the radial and axial supports of an 8 m diameter thin meniscus mirror and the investigations of new technology encoding systems.Paper presented at the Symposium on the JNLT and Related Engineering Developments, Tokyo, November 29–December 2, 1988.     

Rare Earth Deposits of North America

Rare earth elements (REE) have been mined in North America since 1885, when placer monazite was produced in the southeast USA. Since the 1960s, however, most North American REE have come from a carbonatite deposit at Mountain Pass, California, and most of the world’s REE came from this source between 1965 and 1995. After 1998, Mountain Pass REE sales declined substantially due to competition from China and to environmental constraints. REE are presently not mined at Mountain Pass, and shipments were made from stockpiles in recent years. Chevron Mining, however, restarted extraction of selected REE at Mountain Pass in 2007. In 1987, Mountain Pass reserves were calculated at 29 Mt of ore with 8.9% rare earth oxide based on a 5% cut‐off grade. Current reserves are in excess of 20 Mt at similar grade. The ore mineral is bastnasite, and the ore has high light REE/heavy REE (LREE/HREE). The carbonatite is a moderately dipping, tabular 1.4‐Ga intrusive body associated with ultrapotassic alkaline plutons of similar age. The chemistry and ultrapotassic alkaline association of the Mountain Pass deposit suggest a different source than that of most other carbonatites. Elsewhere in the western USA, carbonatites have been proposed as possible REE sources. Large but low‐grade LREE resources are in carbonatite in Colorado and Wyoming. Carbonatite complexes in Canada contain only minor REE resources. Other types of hard‐rock REE deposits in the USA include small iron‐REE deposits in Missouri and New York, and vein deposits in Idaho. Phosphorite and fluorite deposits in the USA also contain minor REE resources. The most recently discovered REE deposit in North America is the Hoidas Lake vein deposit, Saskatchewan, a small but incompletely evaluated resource. Neogene North American placer monazite resources, both marine and continental, are small or in environmentally sensitive areas, and thus unlikely to be mined. Paleoplacer deposits also contain minor resources. Possible future uranium mining of Precambrian conglomerates in the Elliott Lake–Blind River district, Canada, could yield by‐product HREE and Y. REE deposits occur in peralkaline syenitic and granitic rocks in several places in North America. These deposits are typically enriched in HREE, Y, and Zr. Some also have associated Be, Nb, and Ta. The largest such deposits are at Thor Lake and Strange Lake in Canada. A eudialyte syenite deposit at Pajarito Mountain in New Mexico is also probably large, but of lower grade. Similar deposits occur at Kipawa Lake and Lackner Lake in Canada. Future uses of some REE commodities are expected to increase, and growth is likely for REE in new technologies. World reserves, however, are probably sufficient to meet international demand for most REE commodities well into the 21st century. Recent experience shows that Chinese producers are capable of large amounts of REE production, keeping prices low. Most refined REE prices are now at approximately 50% of the 1980s price levels, but there has been recent upward price movement for some REE compounds following Chinese restriction of exports. Because of its grade, size, and relatively simple metallurgy, the Mountain Pass deposit remains North America’s best source of LREE. The future of REE production at Mountain Pass is mostly dependent on REE price levels and on domestic REE marketing potential. The development of new REE deposits in North America is unlikely in the near future. Undeveloped deposits with the most potential are probably large, low‐grade deposits in peralkaline igneous rocks. Competition with established Chinese HREE and Y sources and a developing Australian deposit will be a factor.     

On the kinetics of textural equilibration in forsterite marbles

In the aureole of the Beinn an Dubhaich granite, Skye, the minimum observed median forsterite-calcite-calcite dihedral angle varies from 110° at the olivinein isograd to about 165° (the equilibrium value) at the granite-limestone contact. Laboratory experiments were performed to investigate the kinetics of this textural change. It was found that the rate of change of the forsterite-calcite-calcite dihedral angle followed approximately first-order kinetics with an activation energy of 48±4 kJ mol^-1 for fluid-present conditions, and 90 ±4 kJ mol^-1 for fluid-absent conditions. Scanning ion imaging demonstrated that, at least in the early stages of textural change, solution-reprecipitation of the calcite was the rate determining step in the fluid-present runs. The latter result and the value of the activation energy are both consistent with the activation energy found by previous authors for (albeit zeroth order) silicate-aqueous solution solution-reprecipitation reactions. The value of activation energy for the dry data does not correspond to those for either grain boundary or volume diffusion of oxygen or magnesium in forsterite. The mechanism for textural equilibration in the fluid-absent runs is uncertain. Application of the experimentally-derived rate equation to the Beinn an Dubhaich marbles gave activation energies higher than those obtained experimentally. It is concluded from consideration of grain growth effects that activation energies derived from the Beinn an Dubhaich marbles probably reflect textural equilibration under predominantly fluid-absent conditions.     

Progress in Danube Loess and Paleoenvironment Study

Danube loess, located at the westernmost part of the widespread Eurasian loess belt, is one of the most well-preserved aeolian dust deposits in Europe with the basal age dating back over 1 Ma. Owing to its unique location and formation processes, Danube loess plays an important role in understanding the linkage of climate changes in different climate regimes over Eurasian continent and paleoclimatic changes in middle-high northern latitudes. Major research advances of the Danube loess, including compositions, provenance, chronology, stratigraphy and paleoenvironment changes were systematically reviewed and the focuses of future research were suggested. To better understand loess provenance, the compositions of sediments in all the potential source areas should be investigated, and methodological study of provenance indicators and application of multi-proxies approaches need to be carried out. Chronologically and stratigraphically, feldspar luminescence dating and tephrochronology methods should be widely used, and the establishment of a uniform stratigraphic framework and correlation scheme should be constrained by precise chronology. In terms of the paleoenvironment, it is necessary to conduct high-resolution multi-proxies reconstruction of paleoenviroment for the entire loess-paleosol sequence, extending from the last interglacial period (130 ka to present) to interval of last 1 Ma. The future progress in Danube loess is crucial to improving the study of continental paleoclimate comparison and paleoclimate dynamics over the Eurasian loess region.     

A noble record

Alexander B Verchovsky and Mark A Sephton review the origins and significance of noble gases in meteorites, focusing on what this unique record reveals about the early solar system.     

Spectroscopic Characterization of Organic Structures and Organic‐Inorganic Interactions in Paper Mill Sludge

The organic composition and organic‐inorganic interaction in paper mill sludge (PS) solvent extracts (hexane, ethyl acetate, acetone and ethanol) and humic fractions, humic acid (HA) and humin (HU) were studied by electron paramagnetic resonance spectroscopy (EPR), proton and carbon‐13 nuclear magnetic resonance spectroscopy (¹H NMR; ¹³C NMR), Fourier‐transformed infrared spectroscopy (FTIR), and ultraviolet‐visible spectroscopy (UV‐vis). The strategy of fractionating the PS, sequentially, with organic solvents of increasing polarity is a reliable analytical procedure for humic substance sample separation because it results in more purified fractions. FTIR, ¹H NMR and ¹³C NMR results showed that hexane extract consisted mainly of aliphatic hydrocarbon structures. Their contents in the extracts decreased as the polarity of the extracting solvent increased and the content of oxygen functional groups increased. Carboxylic and carboxylate functional groups were found in the acetone extract, and ester and ether functions were predominantly found in the ethanol extract. EPR spectra revealed some Fe³⁺ complexes with rhombic structure (g₁ = 4.3; g₂ = 9.0) in the humic fractions and in all solvent extracts, except hexane. Quasi‐octahedral Fe³⁺ complexes (g = 2.3; ΔH_pp ≤ 400 G) were found in the HU fraction and in the acetone extract. The organic free radical content in the HA fraction was higher than the non‐fractionated PS sample and HU fraction.     

Rockfalls and rockfall inventory data: Some observations from surprise valley,Jasper National Park,Canada

The major controls of rockfall activity are divided into two interacting groups. (a)Climatic factors which, through their control of temperatures and the availability and state of water, are primary controls of rockfall trigger mechanisms. (b) Geologic factors which, via cliff form (plan, profile, dissection etc.) and the character and availability of materials, influence the type, spatial distribution and intensity of rockfall activity. Detailed examination of these controls suggest that both seasonal and daily patterns of rockfall activity can vary markedly over a very small area. The implications of this variability for the design and interpretation of rockfall inventories are discussed using sample data from Surprise Valley, Jasper National Park, for the period from May-October 1969. On a seasonal basis rockfall activity showed a major spring peak with secondary maxima in the fall and associated with major summer storms. Two sites of differing aspect and morphology were studied in more detail revealing marked differences in the mean hourly frequency (0·94:0·20), mean hourly probability (0·40:0·16, hours with rockfall/hours observed) and daily pattern of rockfall activity. The west facing site showed equal hourly probability of rockfalls from 10⁰⁰ to 20⁰⁰ hr whereas the east facing slope had a greater hourly probability when it was in the sun (11⁰⁰ 14⁰⁰hr) than in the shade (14⁰⁰-19⁰⁰hr). The differences in rockfall frequency and probabilities reflect the physical characteristics of the individual sites whereas the daily pattern of rockfalls is related to microclimate. These results suggest that if future inventory studies are to make a significant contribution, they must be carefully designed field experiments in which. (i) Data are restricted to the study or comparison of single continuously observed sites. (ii) Study sites and/or data periods are carefully selected to isolate and investigate specific controls e.g. the influence of cliff form, aspect, periods of rainfall etc. on rockfall patterns. (iii) Good on-site microclimate data are available. Also comparison of frequency measures based on the arithmetic mean should be avoided since the distribution of rockfalls per hour closely follows a Poisson distribution with occasional high values which unduly influence the value of the arithmetic mean. It is suggested that rockfall probabilities, based on the binary decision of whether or not a rockfall occurs in a given period, are a more useful measure for daily patterns of rockfall activity.