Refining the pattern and style of Cordilleran Ice Sheet retreat: palaeogeography,evolution and implications of lateglacial ice‐dammed lake systems on the southern Fraser Plateau,British Columbia,Canada

Decay of the last Cordilleran Ice Sheet (CIS) near its geographical centre has been conceptualized as being dominated by passive downwasting (stagnation), in part because of the lack of large recessional moraines. Yet, multiple lines of evidence, including reconstructions of glacio‐isostatic rebound from palaeoglacial lake shoreline deformation suggest a sloping ice surface and a more systematic pattern of ice‐margin retreat. Here we reconstructed ice‐marginal lake evolution across the subdued topography of the southern Fraser Plateau in order to elucidate the pattern and style of lateglacial CIS decay. Lake stage extent was reconstructed using primary and secondary palaeo‐water‐plane indicators: deltas, spillways, ice‐marginal channels, subaqueous fans and lake‐bottom sediments identified from aerial photograph and digital elevation model interpretation combined with field observations of geomorphology and sedimentology, and ground‐penetrating radar surveys. Ice‐contact indicators, such as ice‐marginal channels, and grounding‐line moraines were used to refine and constrain ice‐margin positions. The results show that ice‐dammed lakes were extensive (average 27 km²; max. 116 km²) and relatively shallow (average 18 m). Within basins successive lake stages appear to have evolved by expansion, decanting or drainage (glacial lake outburst flood, outburst flood or lake maintenance) from southeast to northwest, implicating a systematic northwestward retreating ice margin (rather than chaotic stagnation) back toward the Coast Mountains, similar in style and pattern to that proposed for the Fennoscandian Ice Sheet. This pattern is confirmed by cross‐cutting drainage networks between lake basins and is in agreement with numerical models of North American ice‐sheet retreat and recent hypotheses on lateglacial CIS reorganization during decay. Reconstructed lake systems are dynamic and transitory and probably had significant effects on the dynamics of ice‐marginal retreat, the importance of which is currently being recognized in the modern context of the Greenland Ice Sheet, where >35% of meltwater streams from land‐terminating portions of the ice sheet end in ice‐contact lakes.     

Active layer hydrology in an arctic tundra ecosystem: quantifying water sources and cycling using water stable isotopes

Climate change and thawing permafrost in the Arctic will significantly alter landscape hydro‐geomorphology and the distribution of soil moisture, which will have cascading effects on climate feedbacks (CO₂ and CH₄) and plant and microbial communities. Fundamental processes critical to predicting active layer hydrology are not well understood. This study applied water stable isotope techniques (δ²H and δ¹⁸O) to infer sources and mixing of active layer waters in a polygonal tundra landscape in Barrow, Alaska (USA), in August and September of 2012. Results suggested that winter precipitation did not contribute substantially to surface waters or subsurface active layer pore waters measured in August and September. Summer rain was the main source of water to the active layer, with seasonal ice melt contributing to deeper pore waters later in the season. Surface water evaporation was evident in August from a characteristic isotopic fractionation slope (δ²H vs δ¹⁸O). Freeze‐out isotopic fractionation effects in frozen active layer samples and textural permafrost were indistinguishable from evaporation fractionation, emphasizing the importance of considering the most likely processes in water isotope studies, in systems where both evaporation and freeze‐out occur in close proximity. The fractionation observed in frozen active layer ice was not observed in liquid active layer pore waters. Such a discrepancy between frozen and liquid active layer samples suggests mixing of meltwater, likely due to slow melting of seasonal ice. This research provides insight into fundamental processes relating to sources and mixing of active layer waters, which should be considered in process‐based fine‐scale and intermediate‐scale hydrologic models. Copyright © 2016 John Wiley & Sons, Ltd.     

The evolution of spinel lherzolite xenoliths and the nature of the mantle at Kilbourne Hole,New Mexico

In peridotites, olivine, clinopyroxene, and orthopyroxene are complex solid solutions with wide stability fields. Depending mostly on bulk composition and pressure, these minerals may be accompanied by plagioclase (low pressure), spinel (moderate pressure), or garnet (high pressure), resulting in 4-phase and rarer 5-phase assemblages. Although a particular mineral assemblage is stable over a range of P–T, the compositions of the individual minerals vary with changing P–T conditions. Application of standard geothermobarometers to olivine–clinopyroxene–orthopyroxene–spinel peridotites is problematic. An alternative approach is to use a bulk rock composition to calculate equilibrium phase diagrams to determine the conditions under which a particular assemblage is stable. This requires consideration of the 7-component system SiO₂–Al₂O₃–Cr₂O₃–FeO–MgO–CaO–Na₂O, internally consistent thermodynamic data for end members, and reliable mixing models for all mineral solutions. Experimental studies in simpler systems, and solution models from the literature, permit derivation of multicomponent thermodynamic mixing models for the key minerals. The models, when applied to xenoliths from Kilbourne Hole, constrain P and T of equilibration and are less sensitive to mineral compositional variations, or uncertainty in activity models, than standard thermobarometry. Our modeling provides the first tightly constrained pressure estimates for Kilbourne Hole, placing the xenoliths in the spinel stability field at depths (30–45 km) that correspond to the uppermost mantle beneath the Rio Grande Rift. The fine-grained equigranular lherzolite, porphyroclastic lherzolite, and some harzburgite-dunite specimens equilibrated at average conditions of 11.5 Kbar-930°C, 12 Kbar-990°C, and 13 Kbar-1,080°C, respectively. The mantle beneath the Rio Grande Rift is layered; the fine-grained equigranular lherzolite derives from relatively shallow depth (35 km average), and the porphyroclastic lherzolite from slightly deeper levels. Lying 5–10 km beneath both lherzolites, the harzburgite-dunite represents a depth where melt extraction has significantly altered mantle chemistry and where local thermodynamic equilibrium has not been maintained.     

The Pre-concentration and determination of Iridium and Palladium in environmental water by imprinted polymer-based method

In this study, the imprinted aniline–formaldehyde was used as an adsorbent for removal of Iridium and Palladium ions from aqueous solutions through batch equilibrium. The sorbent was characterized by fourier transform infrared spectroscopy. The influence of pH, equilibrium time, temperature and initial concentration of metal ions on adsorbed amount of both ions were investigated. The maximum adsorption capacity in initial concentration of 100 mg/L was found to be 12.5 mg/g at pH 7.0 and 14.3 mg/g at pH 8.0 for Iridium and Palladium, respectively. In addition, the best desorption of the metal ions from resin was obtained by 0.5 mol/L nitric acid as eluting agent. The profile of both ions uptake on this sorbent reflects good accessibility of the chelating sites in the imprinted aniline–formaldehyde. Langmuir, Freundlich, Temkin and Redlich–Peterson isotherm models were applied to analyze the experimental data. Moreover, Langmuir linear method was used to obtain the isotherm parameters. However, Langmuir type II achieved the highest coefficient which led to the best fit for the palladium and the best fit for Iridium obtained from linear Redlich–Peterson. However, the thermodynamic parameters (ΔG°, ΔH°, and ΔS°) were also determined using the equilibrium constant values obtained at different temperatures. The results showed that the adsorption for Iridium and Palladium ions was spontaneous nature and endothermic. Moreover, the method was applied for the determination of both ions from tap water samples.     

Old Crow tephra across eastern Beringia: a single cataclysmic eruption at the close of Marine Isotope Stage 6

Old Crow tephra is the largest and most widespread Quaternary eruption presently known in eastern Beringia. Its major- and trace-element geochemistry, Fe-Ti oxides, and stratigraphic and paleoecological context indicate that it is the result of a single cataclysmic eruption. The proximal region may well have experienced tephra fallout from small eruptions just prior to or after the Old Crow event, but there is no evidence to indicate that the distal area was affected. We recalculate the glass fission-track age at 124 ± 10 ka, which, coupled with stratigraphic and paleoenvironmental reconstructions, indicates that deposition occurred prior to development of the last interglacial boreal forest, which suggests a latest Marine Isotope Stage (MIS) 6 age. The bulk tephra volume erupted is estimated by three different approaches, that are in broad agreement at ～200 km³, but this result must be considered as tentative given the poor controls on definition of isopachs over such a large area. The source caldera, although presently unrecognized, is located in the eastern Aleutian arc, possibly at or near the Emmons Lake volcanic center.     

A 15 000‐year record of climate change in northern New Mexico,USA, inferred from isotopic and elemental contents of bog sediments

Elemental (C, N, Pb) and isotopic (δ¹³C, δ¹⁵N) measurements of cored sediment from a small bog in northern New Mexico reveal changes in climate during the Late Pleistocene and Holocene. Abrupt increases in Pb concentration and δ¹³C values ca. 14 420 cal. YBP indicate significant runoff to the shallow lake that existed at that time. Weathering and transport of local volcanic rocks resulted in the delivery of Pb‐bearing minerals to the basin, while a ¹³C‐enriched terrestrial vegetation source increased the δ¹³C values of the sedimentary material. Wet conditions developed over a 300 a period and lasted for a few hundred years. The Younger Dryas period (ca. 12 700–11 500 cal. YBP) caused a reduction in terrestrial productivity reflected in decreasing C/N values, δ¹⁵N values consistently greater than 0‰ and low organic content. By contrast, aquatic productivity increased during the second half of this period, evidenced by increasing δ¹³C values at the time of highest abundance of algae. Dry conditions ca. 8 000–6 000 cal. YBP were characterised by low organic carbon content and high Pb concentrations, the latter suggesting enhanced erosion and aeolian transport of volcanic rock. The range in δ¹³C, δ¹⁵N and C/N values in the sedimentary record fall within the range of modern plants, except during the periods of runoff and drought. The sedimentary record provides evidence of natural climate variability in northern New Mexico, including short‐ (multi‐centennial) and long‐(millennial) term episodes during the Late Pleistocene and Holocene. Copyright © 2010 John Wiley & Sons, Ltd.     

Precision assessment of the orthometric heights determination in northern part of Algeria by combining the GPS data and the local geoid model

The main purpose of this article is to discuss the use of GPS positioning together with a gravimetrically determined geoid, for deriving orthometric heights in the North of Algeria, for which a limited number of GPS stations with known orthometric heights are available, and to check, by the same opportunity, the possibility of substituting the classical spirit levelling. For this work, 247 GPS stations which are homogeneously distributed and collected from the international TYRGEONET project, as well as the local GPS/Levelling surveys, have been used. The GPS/Levelling geoidal heights are obtained by connecting the points to the levelling network while gravimetric geoidal heights were interpolated from the geoid model computed by the Geodetic Laboratory of the National Centre of Spatial Techniques from gravity data supplied by BGI. However, and in order to minimise the discordances, systematic errors and datum inconsistencies between the available height data sets, we have tested two parametric models of corrector surface: a four parameter transformation and a third polynomial model are used to find the adequate functional representation of the correction that should be applied to the gravimetric geoid. The comparisons based on these GPS campaigns prove that a good fit between the geoid model and GPS/levelling data has been reached when the third order polynomial was used as corrector surface and that the orthometric heights can be deducted from GPS observations with an accuracy acceptable for the low order levelling network densification. In addition, the adopted methodology has been also applied for the altimetric auscultation of a storage reservoir situated at 40 km from the town of Oran. The comparison between the computed orthometric heights and observed ones allowed us to affirm that the alternative of levelling by GPS is attractive for this auscultation.     

The impact of discharges from seafood processing on southeastern estuaries

A study to determine the impact of seafood packing and processing effluents discharged to southeastern estuarine waters was conducted in July and August of 1979. The environmental impact of current seafood processing wastes on Georgia’s estuaries appears to be minimal when compared with the natural organic load. One large estuary demonstrated a high residual capacity to receive processing effluents without significant change. The BOD load from shrimp thawing, peeling, sorting, and cleaning operations at a large seafood processing plant was shown to be equivalent to the organic material generated by a 302 m² plot (57 ft×57 ft) of salt marsh. NH₄?N levels were greater than, but the same order of magnitude as, natural runoff from marsh land.     

Reinvestigation of fayalite+anorthite=garnet

The reaction fayalite+anorthite=garnet (GAF) has been investigated in a piston-cylinder apparatus and in an internally heated gas apparatus. Piston-cylinder reversals were obtained at 900 °C (6.0–6.4 kbar), 950 °C (6.3–6.8 kbar), 1000 °C (6.6–7.1 kbar), and 1050 °C (7.0–7.3 kbar). Gas-apparatus experiments yielded a reversal at 7 kbar (993–1049 °C). Results are consistent with earlier experimental studies. Unless garnet Ca–Fe mixing is attended by an excess entropy of at least 2–3 J/K-atom, discrepancies remain between calculated and experimentally determined slopes for GAF. The discrepancy is greater if there is no Al–Si disorder in anorthite. High temperature thermodynamic data for almandine and grossular are needed to help resolve this problem.