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It is often claimed that child English L2 learners take up to seven years to attain English skills commensurate with those of monolingual peers; however, existing research is insufficient to know if this claim is valid for oral language abilities in particular. This study examined the lexical and morphological abilities of English L2 learners and their monolingual peers (ages 12-15; N = 227) in Canadian middle schools to determine the timeline for convergence with monolinguals, and what factors predict individual differences among L2 learners. Having seven or more years of schooling was insufficient for all L2 learners to converge with monolinguals on all measures; moreover, growth in English abilities slowed after seven years. Regression analyses revealed that use of English with friends, parental education, and cognitive skills predicted individual variation in the L2 learners' English abilities and, thus, contributed to their potential for convergence with monolinguals.

High-resolution electron microprobe maps show the distribution of Ti, Al, Ca, K, and Fe among quartz growth zones revealed by scanning electron microscope-cathodoluminescence (SEM-CL) from 12 hydrothermal ore deposits formed between ~100 and ~750 [degrees]C. The maps clearly show the relationships between trace elements and CL intensity in quartz. Among all samples, no single trace element consistently correlates with variations in CL intensity. However in vein quartz from five porphyry-Cu (Mo-Au) deposits, CL intensity always correlates positively with Ti concentrations, suggesting that Ti is a CL activator in quartz formed at >400 [degrees]C. Ti concentrations in most rutile-bearing vein quartz from porphyry copper deposits indicate reasonable formation temperatures of In quartz from most deposits formed at 2000 ppm, but in high-temperature quartz, Al concentrations are consistently in the range of several hundred ppm. Aluminum concentrations in quartz reflect the Al solubility in hydrothermal fluids, which is strongly dependent on pH. Aluminum concentrations in quartz therefore reflect fluctuations in pH that may drive metal-sulfide precipitation in hydrothermal systems. Keywords: quartz, vein, cathodoluminescence, trace elements, hydrothermal, microprobe.

Textures of hydrothermal quartz revealed by cathodoluminescence using a scanning electron microscope (SEM-CL) reflect the physical and chemical environment of quartz formation. Variations in intensity of SEM-CL can be used to distinguish among quartz from superimposed mineralization events in a single vein. In this study, we present a technique to quantify the cathodoluminescent intensity of quartz within individual and among multiple samples to relate luminescence intensity to specific mineralizing events. This technique has been applied to plutonic quartz and three generations of hydrothermal veins at the porphyry copper deposit in Butte, Montana. Analyzed veins include early quartz-molybdenite veins with potassic alteration, pyrite-quartz veins with sericitic alteration, and Main Stage veins with intense sericitic alteration. CL intensity of quartz is diagnostic of each mineralizing event and can be used to fingerprint quartz and its fluid inclusions, isotopes, trace elements, etc., from specific mineralizing episodes. Furthermore, CL intensity increases proportional to temperature of quartz formation, such that plutonic quartz from the Butte quartz monzonite (BQM) that crystallized at temperatures near 750[degrees]C luminesces with the highest intensity, whereas quartz that precipitated at ~250[degrees]C in Main Stage veins luminesces with the least intensity Trace-element analyses via electron microprobe and laser ablation-ICP-MS indicate that plutonic quartz and each generation of hydrothermal quartz from Butte is dominated by characteristic trace amounts of Al, P, Ti, and Fe. Thus, in addition to CL intensity, each generation of quartz can be distinguished based on its unique trace-element content. Aluminum is generally the most abundant element in all generations of quartz, typically between 50 and 200 ppm, but low-temperature, Main Stage quartz containing 400 to 3600 ppm Al is enriched by an order of magnitude relative to all other quartz generations. Phosphorous is present in abundances between 25 and 75 ppm, and P concentrations in quartz show little variation among quartz generations. Iron is the least abundant of these elements in most quartz types and is slightly enriched in CL-dark quartz in pyrite-quartz veins with sericitic alteration. Titanium is directly correlated with both temperature of quartz precipitation, and intensity of quartz luminescence, such that BQM quartz contains hundreds of ppm Ti, whereas Main Stage quartz contains less than 10 ppm Ti. Our results suggest that Ti concentration in quartz is controlled by temperature of quartz precipitation and that increased Ti concentrations in quartz may be responsible for increased CL intensities. Keywords: Butte, porphyry copper, veins, quartz, cathodoluminescence, trace elements, hydrothermal, CL

Scanning electron microscope--cathodoluminescence (SEM-CL) analysis of quartz reveals textures that cannot be observed using optical microscopy or backscattered electrons. These cryptic textures yield insight into timing and physical conditions of quartz growth, especially in environments with multiple quartz-precipitation events. Hydrothermal quartz from quartz-sulfide veins in the porphyry copper deposit in Butte, Montana, was analyzed by SEM-CL, revealing the following textures: euhedral growth zones, wide nonluminescing bands that cut across multiple quartz grains, rounded luminescent quartz grain cores with euhedral overgrowths, nonluminescing 'splatters' of quartz connected by networks of cobweb-like nonluminescing quartz in otherwise luminescent quartz, concentric growth zones, and wide nonluminescent grain boundaries. These textures indicate that many veins have undergone fracturing, dilation, growth of quartz into fluid-filled space, quartz dissolution, and recrystallization of quartz. Precipitation and dissolution textures indicate that early quartz-molybdenite veins formed as a result of pressure fluctuations between lithostatic and hydrostatic at high temperatures, and later pyrite-quartz veins formed near hydrostatic pressure in response to temperature decrease through and beyond the field of retrograde quartz solubility. Keywords: Butte, cathodoluminescence, fluid inclusions, hydrothermal, quartz, veins.

This paper evaluates controls on cassiterite crystallization under hydrothermal conditions based on the textural setting and geochemistry of cassiterite from six different mineralization environments from the world-class Gejiu tin district, southwest China. The cassiterite samples feature diverse internal textures, as revealed by cathodoluminescence (CL) imaging, and contain a range of trivalent (Ga, Sc, Fe, Sb), quadrivalent (W, U, Ti, Zr, Hf), and pentavalent (Nb, Ta, V) trace elements, with Fe, Ti, and W being the most abundant trace elements. Cassiterite Ti/Zr ratios tend to decrease with distance away from the causative granite intrusion, and so has potential to be used as a broad tool for vectoring toward a mineralized intrusive system. Elemental mapping of cassiterite grains reveals that trace-element concentration variations correspond closely to CL zoning patterns. The exceptions are distinct irregular domains that sharply cut across the primary oscillatory zoning, as defined by the concentrations of W, U, Sb, and Fe. These zones are interpreted to have formed after primary cassiterite growth via fluid-driven dissolution-reprecipitation processes. Zones with low W and U (and Sb) and high Fe are interpreted to have formed during interaction with relatively oxidized fluids in which W and U are stripped from cassiterite due to cation exchange with Fe3+. Systematics of W, U, Sb, and Fe partitioning into cassiterite can, therefore, be used as a monitor of the relative oxidation state of the hydrothermal fluid from which cassiterite precipitates. Cassiterite U-Pb geochronology results obtained by LA-ICP-MS return ages between 77 and 83 Ma, which is consistent with previous geochronology from the region. Ages determined on zones of dissolution-reprecipitation are similar to ages for primary cassiterite growth, indicating a short (<3 m.y.) timespan of hydrothermal activity. These results confirm the potential of U-Pb dating of cassiterite for directly constraining the timing of Sn deposition. [ABSTRACT FROM AUTHOR]