Microalgal Communities of the Sea Ice, Ice-Covered and Ice-Free Waters of Wood Bay (Ross Sea, Antarctica) During the Austral Summer 1993 – 94

Abstract. During the austral summer 1993 – 94, microalgal density and biomass were investigated in the sea ice, in the underlying water column, in the melt water and during the formation of the sea ice. Of the 96 taxa identified, 59 were diatoms and 32 were dinoflagellates. Among the remaining five species, Pseudopleurochloris antarctica  was very abundant both in the sea ice and in the ice-free waters. Cell densities and biomass of microalgae were higher in the bottom of the sea ice and during the formation of the ice than in the seawater, and diatoms were the dominant group at higher microalgal biomass. Among these, Entomoneis kufferathii , Chaetoceros dichaeta and Fragilariopsis species were the most common taxa.     

Origins of non-equilibrium lithium isotopic fractionation in xenolithic peridotite minerals: Examples from Tanzania

Olivine, clinopyroxene and orthopyroxene in variably metasomatised peridotite xenoliths from three lithospheric mantle sections beneath the East African Rift in Tanzania (Lashaine, Olmani, Labait) show systematic differences in their average Li concentrations (2.4 ppm, 2.0 ppm and 1.5 ppm, respectively) and intermineral isotopic fractionations, with olivine being heaviest (δ⁷Li = + 2.3 to + 13.9‰, average + 5.0‰), followed by orthopyroxene (? 4.1 to + 6.5‰, average + 0.8‰) and clinopyroxene (? 6.7 to + 4.1‰, average ? 1.6‰). These features are ascribed to the effects of kinetic Li isotope fractionation combined with different Li diffusivities in mantle minerals.Two main mechanisms likely generate diffusion-driven kinetic Li isotope fractionation in mantle xenoliths (1) Li diffusion from grain boundary melt into minerals during recent metasomatism or entrainment in the host magma and (2) subsolidus intermineral Li-redistribution. The latter can produce both isotopically light (Li-addition) and heavy (Li-loss) minerals and may occur in response to changes in pressure and/or temperature.Modelling shows that non-mantle-like δ⁷Li in clinopyroxene (< + 2‰), combined with apparent equilibrium olivine-clinopyroxene elemental partitioning in most peridotite xenoliths from all three Tanzanian localities probably reflects incipient Li addition during interaction with the host magma. Low δ⁷Li (< ? 3‰), combined with high Li concentrations (> 3 ppm) in some clinopyroxene may require very recent (minutes) Li ingress from a Li-rich melt (100s of ppm) having mantle-like δ⁷Li. This might happen during late fragmentation of some mantle xenoliths caused by a volatile- (and Li-) rich component exsolved from the host basalt. In contrast, high Li concentrations (> 2 ppm) and δ⁷Li (> 4‰) in olivine from many Labait and Olmani samples are attributed to an older, pre-entrainment enrichment event during which isotopic equilibrium was attained and whose signature was not corrupted during xenolith entrainment. Low Li concentrations and mantle-like isotopic composition of olivine from most Lashaine xenoliths indicate limited metasomatic Li addition.Thus, Li concentrations and isotope compositions of mantle peridotites worldwide may reflect two processes, with olivine mainly preserving a signature of depletion in refractory samples (low Li contents and δ⁷Li) or of older (precursory) melt addition in metasomatised samples (high Li contents and δ⁷Li), while non mantle-like, low δ⁷Li in almost all clinopyroxene can be due to Li ingress during transport in the host magma and/or slow cooling, if the samples were erupted in lavas. In Tanzania, the peridotites experienced rift-related heating prior to entrainment and were quenched upon eruption, so Li ingress is the most likely process responsible for the isotopically light clinopyroxene here.     

Li and δLi in mudrocks from the British Caledonides: Metamorphism and source influences

Mudrocks from three lower Paleozoic basins in the British Caledonides (southern Lake District, northern Lake District and Southern Uplands) were investigated to determine the influence of sub-greenschist facies metamorphism on Li and the factors that control Li in fine-grained terrigenous sedimentary rocks. Metamorphic grade, as determined by KI (Kübler index) does not correlate with Li content ([Li]) and δ⁷Li, indicating that sub-greenschist facies metamorphism has negligible effect on Li in these rocks. Collectively, the data for all three basins show a negative correlation between [Li] and δ⁷Li and a positive correlation between [Li] and the Chemical Index of Alteration (CIA), suggesting that provenance exerts the greatest control on Li in mudrocks. Samples from the northern Lake District, which were deposited in an extensional basin, have homogeneous REE patterns, similar to shale composites (PAAS), the highest CIA, Th/U and [Li] and the lowest δ⁷Li and ε_Nd, consistent with their derivation from a highly weathered, ancient continental source. By contrast, mudrocks from the Southern Uplands range to the lowest CIA, Th/U and [Li] and have the highest δ⁷Li and ε_Nd. These samples were deposited in a forearc basin on the southern margin of the Laurentian craton and contain volcanic detritus. Their REE patterns are the most variable, ranging from average shale-like patterns to less LREE-enriched patterns. The compositional heterogeneity within the Southern Uplands mudrocks is consistent with a mixed provenance that includes juvenile crustal materials (lower [Li], ε_Nd and Th/U, higher δ⁷Li), likely derived from the arc, as well as more highly weathered continental detritus. Mudrocks from the southern Lake District were deposited in a foreland basin, and exhibit geochemical characteristics intermediate between the northern Lake District and the Southern Uplands mudrocks, indicating their derivation from a mixed source. Our study shows that Li concentrations and δ⁷Li can provide additional information on the degree of weathering of the provenance of mudrocks.     

Toward quantification of strain‐related mosaicity in shocked lunar and terrestrial plagioclase by in situ micro‐X‐ray diffraction

Studies of shock metamorphism of feldspar typically rely on qualitative petrographic observations, which, while providing invaluable information, can be difficult to interpret. Shocked feldspars, therefore, are now being studied in greater detail by various groups using a variety of modern techniques. We apply in situ micro‐X‐ray diffraction (μXRD) to shocked lunar and terrestrial plagioclase feldspar to contribute to the development of a quantitative scale of shock deformation for the feldspar group. Andesine and labradorite from the Mistastin Lake impact structure, Labrador, Canada, and anorthite from Earth's Moon, returned during the Apollo program, were examined using optical petrography and assigned to subgroups of the optical shock level classification system of Stöffler (1971). Two‐dimensional μXRD patterns from the same samples revealed increased peak broadening in the chi dimension (χ), due to strain‐related mosaicity, with increased optical signs of deformation. Measurement of the full width at half maximum along χ (FWHMχ) of these peaks provides a quantitative way to measure strain‐related mosaicity in plagioclase feldspar as a proxy for shock level.     

A lithium isotopic study of sub-greenschist to greenschist facies metamorphism in an accretionary prism,New Zealand

To investigate the behavior of Li during low-grade metamorphism and fluid flux in an accretionary prism we measured the Li concentrations ([Li]) and isotopic compositions (δ⁷Li) of sub-greenschist and greenschist-facies Otago Schist composites, as well as cross-cutting quartz veins, which are interpreted to have precipitated from slab-derived fluids. The average [Li] of sub-greenschist facies composites (41 ± 13 μg/g, 2σ) is statistically distinct (97% confidence level, student t test) to that of greenschist facies composites (34 ± 9 μg/g, 2σ), which have experienced mass addition of silica in the form of quartz veins having [Li] between 0.4–2.3 μg/g. A linear regression of the correlation between [Li] and calculated mass additions suggests that the depletion of [Li] in greenschist facies composites is due to both dilution from the addition of the quartz veins, as well as metamorphic dehydration. The [Li] of both groups of composites correlates with their CIA (Chemical Index of Alteration) values (50–58), which are low, consistent with the inferred graywacke protolith of the Otago Schist. The δ⁷Li of sub-greenschist and greenschist facies composites are remarkably constant, with an average δ⁷Li of 0.2 ± 1.7 (2σ) and ?0.5 ± 1.9 (2σ), respectively, and comparable to that of the average upper continental crust. Thus, metamorphism has had no discernable effect on δ⁷Li in these samples. The Li isotopic signature of the schists is similar to that seen in pelitic sedimentary rocks and likely reflects the δ⁷Li of the protoliths. The surprisingly light δ⁷Li of the quartz veins (?2.8 to ?1.4) likely records kinetic fractionation associated with Li ingress into the veins from surrounding wallrock.An isotopic equilibrium fluid flow model indicates that: 1) if the [Li] of slab-derived fluids is less than a few μg/g, the δ⁷Li of the overlying lithologies (i.e., the schists) is not significantly influenced by the fluid flux, regardless of the δ⁷Li of the fluids, 2) the slab-derived fluids will have heavy δ⁷Li of > + 10 after reacting with the prism sediments during their ascent, and 3) the [Li] of the slab-derived fluids is likely in the range of 0 < [Li] ≤ 41(μg/g). Thus, isotopically heavy slab-derived fluids that traverse sediments in accretionary prisms may leave little trace in the rocks and their surface compositional characteristics will reflect the net result of their interaction with the sediments of the prism.     

Rebel with a cause? Iconography and public memory in the Southern United States

Recent years have witnessed debates in the American South between traditional white Southerners and African American Southerners over whether and how symbols from the region's two defining historical events – the Civil War and the Civil Rights movement – are displayed on the region's landscape. This paper examines the most contentious of these debates, the conflict over government sanction for flying the various flags of the Confederate States of America. This article first discusses the concepts of iconography and public memory, and then the role of Confederate flags in traditional white Southern iconography. We then examine four recent attempts in the states of Georgia, Alabama and South Carolina, and within the chambers of the U.S. Senate to remove government sanction for flying Confederate flags. We conclude from these debates that while icons can act as centripetal forces binding a people together, they can also emerge as centrifugal forces, further splitting apart a region's population along major cultural and racial divisions.     

Gel synthesis of magnesium silicates: A 29Si magic angle spinning NMR study

The formation of the magnesium silicate minerals forsterite, enstatite, and roedderite by heating of amorphous “protosilicate” gels precipitated from aqueous solution has been studied by ²⁹Si MAS nmr. Gentle drying of the hydrogels at 110° C gives materials with broad nmr signals that do not differ appreciably with preparation conditions, but the minerals formed by heating at 750° C or higher are greatly dependent on the precipitation and washing conditions of the original gel. The rare mineral roedderite, best known from studies of unequilibrated enstatite chondrite meteorites, becomes a major species along with forsterite when the hydrogels are washed with sodium hydroxide solution before drying and heating to 750° C.     

New Compositional and Structural Constraints on the Smithsonian Microanalytical Reference Materials: Amphiboles from Kakanui and Arenal

The amphiboles from Kakanui and Arenal are two natural minerals that have been used worldwide as microanalytical reference materials, but their compositions and crystal structures are still poorly constrained. In this paper, we report new data on H₂O and trace element mass fractions and single-crystal structural refinement of these two amphiboles. H₂O mass fractions of the Kakanui and Arenal amphiboles determined via Karl-Fischer titration are 0.92 ± 0.18 (2s) and 1.56 ± 0.22% m/m (2s), respectively; these values estimated based on crystal-structure refinement are 0.86 and 1.46% m/m, respectively. Trace element mass fractions measured via LA-ICP-MS in two laboratories are in good agreement, and spots from five fragments for both Kakanui and Arenal amphiboles are generally consistent within reproducibility precision (2s). Our measurements indicate a better homogeneity for the amphiboles from Kakanui than that from Arenal. According to the latest scheme for amphibole classification and nomenclature (Hawthorne et al. 2012), the sample from Arenal is a (partially dehydrogenated) pargasite, and that from Kakanui is a kaersutite. The significant amount of oxo-component and that ^CTi⁴⁺ content is strongly ordered at the M(1) site for both amphiboles indicate crystallisation under high fO₂ conditions.     

Fluid inclusions in high-grade gneisses of the Kapuskasing structural zone,Ontario: metamorphic fluids and uplift/erosion path

Fluid inclusions in quartz grains from five samples of high-grade rocks (two paragneisses, an amphibolite, a mafic gneiss and a tonalite dike) from the 2.7 Ga Kapuskasing structural zone (KSZ), Ontario, were examined with petrographic, microthermometric and laser Raman techniques. Three types of fluid inclusions were observed: CO₂-rich, H₂O-rich and mixed CO₂-H₂O. CO₂-rich fluid inclusions are pseudosecondary or secondary in nature and are generally pure CO₂; a few contain varying amounts of CH₄·H₂O-rich fluid inclusions are secondary in nature, contain variable amounts of dissolved salts, and generally contain daughter crystals. Mixed CO₂-H₂O fluid inclusions occur where trails of H₂O-rich inclusions intersect trails of CO₂-rich inclusions. Isochores for high density (p=1.03 g/cm³) pseudosecondary, pure CO₂ inclusions intersect the lower pressure portion of the estimated P-T field for high-grade metamorphism, implying that pure CO₂ was the peak metamorphic fluid. The variable CH₄ content of CO₂ inclusions within graphite-bearing samples suggests that CH₄ was introduced locally after the formation of the CO₂ inclusions; however the origin of the CH₄ remains problematic. An aqueous fluid clearly penetrated the gneisses after the peak metamorphism (during uplift/erosion), forming secondary inclusions and contributing to the minor retrogressive hydration observed in these rocks. The presence of the pseudosecondary, high-density CO₂ inclusions in quartz crystals in the KSZ rocks constrains the uplift/ erosion path for the KSZ to one of simultaneous decrease in pressure and temperature.