Inheritance of smolting phenotypes in backcrosses of hybrid stream-type × ocean-type chinook salmon (Oncorhynchus tshawytscha)

Chinook salmon (Oncorhynchus tshawytscha) are ecologically and geographically differentiated into two life history types: “ocean-type,” which enter estuaries as fry or fingerlings in the first year of life and rear there for up to 6 wk before migrating to sea, and “stream-type,” which migrate seaward as smolts after one or more years in fresh water and are only transient residents in the outer portion of estuaries. Following exposure to a long-day priming photoperiod for 2 mo from the time of first feeding, progeny of stream-type chinook salmon undergo a reduction in growth during summer and remain as parr, whereas progeny of ocean-type chinook salmon and hybrids continue to grow during the summer and develop into underyearling smolts. Male purebred and hybrid F₁ progeny of ocean-type and stream-type chinook salmon were backcrossed to females of both parental populations to examine the segregation of photoperiod-independent (smolt) and photoperiod-dependent (parr) phenotypes among progeny. Results of the backcrosses of the hybrid F₁ males depended on female type. The backcross to ocean-type females produced progeny that were predominantly smolts, whereas progeny from the backcross to stream-type females segregated into approximately equal numbers of smolts and parr. These results are consistent with Mendelian inheritance of a single major gene with two alleles: a dominant allele for the photoperiod-independent phenotype of ocean-type chinook salmon and a recessive allele for the photoperiod-dependent phenotype of stream-type chinook salmon.     

Submarine exhalative gold mineralization at the London-Virginia Mine,Buckingham County,Virginia

Low grade submarine exhalative gold mineralization occurs at the London-Virginia deposit in central Virginia Piedmont. The deposit consists of a series of localized but conformable units — basal garnetiferous-chlorite schist, magnetite schist, quartz-muscovite schist, ferruginous quartzite, and chlorite-biotite schist — which represent a mixture of submarine epiclastic volcanic debris and exhalative chemical sediments. Finely disseminated gold occurs dispersed with minor amounts of pyrite, sphalerite, chalcopyrite, galena, and tennantite in the ferruginous quartzite and quartz-muscovite schist. The deposit is believed to have formed by processes analogous to those currently active in the Atlantis II Deep of the Red Sea. Silicarich, hypersaline brines discharged through fractures in the sea floor and ponded in a local basin. Epiosodic influx of clastic debris and extensive deposition of hydrothermal silica diluted the concentration of sulfides and gold to produce a low-grade, siliceous mineralized zone. Emanation from the exhalative vent was terminated when the basin was capped by a lava flow. Subsequent regional greenschist grade metamorphism has recrystallized the silica into a granular quartzite and produced minor remobilization of the gold and sulfides.     

Predicted relative sea-level changes (18,000 years B.P. to present) caused by late-glacial retreat of the Antarctic Ice Sheet

Predictions of global changes in relative sea level caused by retreat of the Antarctic Ice Sheet from its 18,000 yr B.P. maximum to its present size are calculated numerically. When combined with the global predictions of relative sea-level change resulting from retreat of the Northern Hemisphere ice sheets, the results may be compared directly to observations of sea-level change on the Antarctic continent as well as at distant localities. The comparison of predictions to the few observations of sea-level change on Antarctica supports the view that the Antarctic Ice Sheet was larger 18,000 years ago than at present. The contribution of the Antarctic Ice Sheet to the total eustatic sea-level rise is assumed to be 25 m (25% of the assumed total eustatic rise). If as little as 0.7 m of this 25-m rise occurred between 5000 yr B.P. and the present, few mid-oceanic islands would emerge. If the Antarctic Ice Sheet attained its present dimensions by 6000 yr B.P., however, and if the volume of the ocean has remained constant for the past 5000 years, numerous islands throughout the Southern Hemisphere would emerge. It is suggested that a thorough study of Pacific islands, believed by some to have slightly emerged shorelines of Holocene age, would yield useful information about ocean volume changes during the past 5000 years, and hence on the glacial history of the Antarctic Ice Sheet.     

Systematics of the spinel structure type

Systematic trends in the geometry of 149 oxide and 80 sulfide binary and ternary spinels have been examined from the standpoint of ionic radius and electronegativity. The mean ionic radii of the octahedral and tetrahedral cations, taken together, account for 96.9 and 90.5% of the variation in the unit cell parameter, a, of the oxides and sulfides, respectively, with the octahedral cation exerting by far the dominant influence in sulfides. The mean electronegativity of the octahedral cation exerts an additional, but small, influence on the cell edge of the sulfides. The equation a=(8/3√d)d _tet+(8/3)d _oct, where d _tet and d _oct are the tetrahedral and octahedral bond lengths obained from the sum of the ionic radii, accounts for 96.7 and 83.2% of the variation in a in the oxides and sulfides, respectively, again testifying to the applicability of the hard-sphere ionic model in the case of the spinel structure. Comparison of observed and calculated u values for 94 spinels indicates that up to 40% of the experimentally measured anion coordinates may be significantly in error. In addition to these compounds, u values are given for 52 spinels for which no data have previously been determined. Diagrams are presented for the rapid interpretation of the internal consistency of published data and the prediction of the structural parameters of hypothetical or partially studied spinels.     

Pyrite: physical and chemical textures

Pyrite may crystallize initially in forms as diverse as framboids or cubes depending upon the temperatures and pressures. Fluid-rich diagenesis or low-grade metamorphism clearly results in thorough recrystallization and the common formation of cubes. Once these have formed, the pyrite becomes much more refractory and retains many characteristics even in deposits which have undergone penetrative deformation. This is in strong contrast to the behavior of most of the accompanying sulfides, which often undergo ductile deformation, solid state or chemical remobilization, and annealing. Pyrite deforms sparingly until there is brittle failure; however, there may be significant pyrite corrosion and regrowth during metamorphism as the result of sulfur exchange with other minerals, especially pyrrhotite. Pyrite fabrics may also be significantly modified by pressure solution or Coble creep. Optical microscopic examination and electron microprobe chemical mapping of pyrites from a variety of mineral deposits, including several high-grade metamorphic ones, reveals that the pyrites frequently contain both physical and chemical textures that may be interpreted in terms of the depositional and the post-depositional history of the deposits. Inclusions of sulfides or other minerals reveal information on the timing of the crystallization or recrystallization of the pyrite; chemical mapping of elements such as Ni, Co, and As reveals information on the relative time of transport of these elements in the ore fluids. Received: 19 March 1997 / Accepted: 14 May 1998     

The 14-year Performance of a Compacted Clay Liner used as Part of a Composite Liner System for a Leachate Lagoon

The migration of contaminants through a 2.9 m thick compacted clay liner (CCL) for a landfill leachate lagoon is examined 14 years after construction. The clay liner formed the lower portion of the composite liner system but the geomembrane (GM) was found to have defects that had allowed leachate to migrate between the GM and CCL. Chloride, sodium, potassium, calcium and magnesium pore water profiles through the CCL are examined. It is shown that chloride migrated approximately 1.7 m into the CCL during the 14 years of the lagoon operation, sodium approximately 1.2 m, and potassium 0.7 m. Diffusion and sorption data from laboratory diffusion testing are utilized in combination with a finite layer contaminant transport model to predict field contaminant migration profiles through the composite liner system and to establish the time of ‘failure’ of the geomembrane at sometime between 0 and 6 years after installation. Relatively high sorptive uptake of potassium by the CCL soil is observed from batch testing and diffusion testing with field data suggesting an even larger amount of sorption. It is hypothesized that organic sludge matter at the base of the lagoon is responsible for potassium uptake from the leachate. This field case highlights the importance of the compacted clay liner as part of the composite liner system in acting as a diffusion barrier during the lifetime of the lagoon as well as using relatively non-conservative contaminants such as chloride and sodium to estimate geomembrane ‘failure’ times     

Spatially controlled Fe and Si isotope variations: an alternative view on the formation of the Torres del Paine pluton

We present new Fe and Si isotope ratio data for the Torres del Paine igneous complex in southern Chile. The multi-composition pluton consists of an approximately 1 km vertical exposure of homogenous granite overlying a contemporaneous 250-m-thick mafic gabbro suite. This first-of-its-kind spatially dependent Fe and Si isotope investigation of a convergent margin-related pluton aims to understand the nature of granite and silicic igneous rock formation. Results collected by MC-ICP-MS show a trend of increasing δ⁵⁶Fe and δ³⁰Si with increasing silica content as well as a systematic increase in δ⁵⁶Fe away from the mafic base of the pluton. The marginal Torres del Paine granites have heavier Fe isotope signatures (δ⁵⁶Fe = +0.25 ± 0.02 2se) compared to granites found in the interior pluton (δ⁵⁶Fe = +0.17 ± 0.02 2se). Cerro Toro country rock values are isotopically light in both Fe and Si isotopic systems (δ⁵⁶Fe = +0.05 ± 0.02 ‰; δ³⁰Si = ?0.38 ± 0.07 ‰). The variations in the Fe and Si isotopic data cannot be accounted for by local assimilation of the wall rocks, in situ fractional crystallization, late-stage fluid exsolution or some combination of these processes. Instead, we conclude that thermal diffusion or source magma variation is the most likely process producing Fe isotope ratio variations in the Torres del Paine pluton.     

Complex zoning between super-calcic pigeonite and augite from the Graveyard Point sill, Oregon: a record of the interplay between bulk and interstitial liquid fractionation

The 150 m thick late Miocene Graveyard Point sill (GPS) is situated at the Idaho-Oregon border near the southwestern edge of the western Snake River Plain. It records from bottom to top continuous fractional crystallization of a tholeiitic parent magma (lower chilled border, FeO/(FeO+MgO) = 0.59, Ni = 90 ppm) towards granophyres (late pods and dikes, FeO/(FeO+MgO) = 0.98, 78 wt% SiO₂ 3.5 wt% K₂O, <4 ppm Ni) showing a typical trend of Fe and P enrichment. Fractionating minerals are olivine (Fo₇₉-Fo₂), augite (X _Fe = 0.18−0.95), feldspars (An₈₀Or₁-An₁Or₆₂), Fe-Ti oxides (Ti-rich magnetite and ilmenite), apatite and in two samples super-calcic pigeonite (Wo_18–28 Fs_41–54). The granophyres may bear some quartz. Compositionally zoned minerals record a large interval of the fractionation process in every single sample, but this interval changes with stratigraphic height. In super-calcic pigeonite-bearing samples, olivine is scarce or lacking and because super-calcic pigeonite occurs as characteristic overgrowths on augite, its formation is interpreted to be related to the schematic reaction: augite + olivine (component in melt) + SiO₂ (in melt) = pigeonite, that defines the cotectic between augite and pigeonite in olivine-saturated basaltic systems. Line measurements with the electron microprobe reveal that the transition from augite to super-calcic pigeonite is continuous. However, some crystals show an abrupt “reversal” towards augite after super-calcic pigeonite growth. Two processes compete with each other in the GPS: fractional crystallization of the bulk liquid (the bulk melt separates from solids and interstitial liquids in the solidification front) and fractional crystallization of interstitial melt in the solidification front itself. Interplay between those two processes is proposed to account for the observed variations in mineral chemistry and mineral textures. Received: 25 November 1998 / Accepted: 14 June 1999     

A New Appraisal of Sri Lankan BB Zircon as a Reference Material for LA‐ICP‐MS U‐Pb Geochronology and Lu‐Hf Isotope Tracing

A potential zircon reference material (BB zircon) for laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) U‐Pb geochronology and Hf isotope geochemistry is described. A batch of twenty zircon megacrysts (0.5–1.5 cm³) from Sri Lanka was studied. Within‐grain rare earth element (REE) compositions are largely homogeneous, albeit with some variation seen between fractured and homogeneous domains. Excluding fractured cathodoluminescence bright domains, the variation in U content for all analysed crystals ranged from 227 to 368 μg g^?1 and the average Th/U ratios were between 0.20 and 0.47. The Hf isotope composition (0.56–0.84 g/100 g Hf) is homogeneous within and between the grains – mean ¹⁷⁶Hf/¹⁷⁷Hf of 0.281674 ± 0.000018 (2s). The calculated alpha dose of 0.59 × 10¹⁸ g^?1 for a number of BB grains falls within the trend of previously studied, untreated zircon samples from Sri Lanka. Aliquots of the same crystal (analysed by ID‐TIMS in four different laboratories) gave consistent U‐Pb ages with excellent measurement reproducibility (0.1–0.4% RSD). Interlaboratory assessment (by LA‐ICP‐MS) from individual crystals returned results that are within uncertainty equivalent to the TIMS ages. Finally, we report on within‐ and between‐grain homogeneity of the oxygen isotope systematic of four BB crystals (13.16‰ VSMOW).