Stable carbon-isotopic compositions of lipids isolated from the ammonia-oxidizing chemoautotroph Nitrosomonas europaea

For the ammonia-oxidizing bacterium Nitrosomonas europaea, grown autotrophically using semicontinuous culturing, average biomass was depleted in ¹³C relative to CO₂ dissolved in the medium by ca. 20‰ and the total-lipid extract was depleted in ¹³C relative to biomass by 3.7‰. The n-alkyl lipids (weighted average of fatty acids) and isoprenoid lipids (weighted average of hopanoids) were both depleted in ¹³C relative to biomass by about 9‰. The large depletion in the isoprenoid lipids seems to indicate that isotopic fractionations associated with the biosynthesis of methylerythritol phosphate (MEP) affected at least two carbon positions in each isoprene unit. Among the fatty acids, trans-9-hexadecenoic acid was most depleted (13.0‰ relative to biomass), followed by cis-9- hexadecenoic acid (9.6‰) and hexadecanoic acid (6.9‰). Isotopic relationships between the three acids suggest that significant isotope effects were associated with the desaturation and cis to trans isomerization of fatty acids. Given these observations, hopanoids produced by ammonia-oxidizing bacteria growing in natural waters are likely to be depleted in ¹³C by 26–30‰ relative to dissolved CO₂. Since CO₂ at aquatic oxyclines is often depleted in ¹³C, the range of δ values expected for hopanoids is ca. −34‰ to −55‰. The δ values of geohopanoids observed in numerous studies and attributed to unspecified chemoautotrophs fall within this range.     

Ionospheric Scintillation and Dynamics of Fresnel-Scale Irregularities in the Inner Region of the Equatorial Ionization Anomaly

This paper reports differences in the occurrence statistics of global positioning system (GPS) L-band scintillations at observational sites located in the inner regions of the northern and southern crests of the equatorial ionization anomaly. Ground-based GPS data acquired at the closed magnetically aligned stations of Manaus (3.1°S; 59.9°W; dip lat. 6.2°N) and Cuiabá (15.5°S; 56.1°W; dip. lat. 6.2°S), Brazil, from December 2001 to February 2007 are used in the analysis. The drift dynamics of Fresnel-scale ionospheric irregularities at the southern station of Cuiabá are also investigated. Only geomagnetically quiet days with the sum of daily Kp < 24 were used in the analysis statistics and in the irregularity drift studies. The results reveal a clear dependence of the scintillation occurrence with the solar activity, but there exists an asymmetry in the percentage of scintillation occurrence between the two stations throughout the period analyzed. The nocturnal occurrence of the scintillations over Cuiabá is predominantly larger than over Manaus, but this scenario seems to change with the decline in the solar activity (mainly during local post-midnight hours). A broad minimum and maximum in the scintillation occurrence appears to occur over both the stations, respectively, during the June solstice (winter) and December solstice (summer) months. The dynamics of the Fresnel-scale irregularities, as investigated from the estimations of the mean zonal drift velocities, reveals that the amplitude of the eastward drifts tends to reduce with the decline in the solar activity. The magnitude of the zonal drift velocities during the December solstice months is larger than during the equinoxes, with the differences being more pronounced at solar maximum years. Other relevant aspects of the observations, with complementary data from a low-latitude ionospheric model, are highlighted and discussed.     

FRAGMENTAL BRECCIAS AND THE COLLISIONAL EVOLUTION OF ORDINARY CHONDRITE PARENT BODIES

Our survey of type 4–6 ordinary chondrites indicates that gas-poor, melt-rock and/or exotic clast-bearing fragmental breccias constitute 5%, 22% and 23%, respectively, of H, L and LL chondrites. These abundances contrast with the percentages of solar-gas-rich regolith breccias among ordinary chondrites: H (14%), L (3%) and LL (8%) (Crabb and Schultz, 1981). Petrologic study of several melt-rock-clast-bearing fragmental breccias indicates that some acquired their clasts prior to breccia metamorphism and others acquired them after metamorphism of host material. In general, the melt-rock clasts in gas-poor H chondrite fragmental breccias were acquired after breccia metamorphism and were probably formed by impacts into boulders or exposed outcrops of H4-6 material in the H chondrite parent body regolith. In contrast, most of the melt-rock clasts in gas-poor L and LL fragmental breccias were acquired prior to breccia metamorphism. The low abundance of regolith breccias among L chondrites and evidence that at least two-thirds of the L chondrites suffered a major shock event 0.5 Gyr ago, suggest that the L parent body may have been disrupted by a major collision at that time and that the remaining parent body fragments were too small to develop substantial regoliths (e.g., Heymann, 1967; Crabb and Schultz, 1981). Such a disruption would have exposed a large amount of L chondrite bedrock, some of which would consist of fragmental breccias that acquired melt-rock clasts very early in solar system history, prior to metamorphism. The exposed bedrock would serve as a potential target for sporadic meteoroid impacts to produce a few fragmental breccias with unmetamorphosed melt-rock clasts. The high proportion of genomict brecciated LL chondrites reflects a complex collisional history, probably including several episodes of parent body disruption and gravitational reassembly. Differences in the abundances of different kinds of breccias among the ordinary chondrite groups are probably due to the stochastic nature of major asteroidal collisions.     

Mineralogy of meteorite groups

Abstract— Approximately 275 mineral species have been identified in meteorites, reflecting diverse redox environments, and, in some cases, unusual nebular formation conditions. Anhydrous ordinary, carbonaceous and R chondrites contain major olivine, pyroxene and plagioclase; major opaque phases include metallic Fe-Ni, troilite and chromite. Primitive achondrites are mineralogically similar. The highly reduced enstatite chondrites and achondrites contain major enstatite, plagioclase, free silica and kamacite as well as nitrides, a silicide and Ca-, Mg-, Mn-, Na-, Cr-, K- and Ti-rich sulfides. Aqueously altered carbonaceous chondrites contain major amounts of hydrous phyllosilicates, complex organic compounds, magnetite, various sulfates and sulfides, and carbonates. In addition to kamacite and taenite, iron meteorites contain carbides, elemental C, nitrides, phosphates, phosphides, chromite and sulfides. Silicate inclusions in IAB/IIICD and IIE iron meteorites consist of mafic silicates, plagioclase and various sulfides, oxides and phosphates. Eucrites, howardites and diogenites have basaltic to orthopyroxenitic compositions and consist of major pyroxene and calcic plagioclase and several accessory oxides. Ureilites are made up mainly of calcic, chromian olivine and low-Ca clinopyroxene embedded in a carbonaceous matrix; accessory phases include the C polymorphs graphite, diamond, lonsdaleite and chaoite as well as metallic Fe-Ni, troilite and halides. Angrites are achondrites rich in fassaitic pyroxene (i.e., Al-Ti diopside); minor olivine with included magnesian kirschsteinite is also present. Martian meteorites comprise basalts, lherzolites, a dunite and an orthopyroxenite. Major phases include various pyroxenes and olivine; minor to accessory phases include various sulfides, magnetite, chromite and Ca-phosphates. Lunar meteorites comprise mare basalts with major augite and calcic plagioclase and anorthositic breccias with major calcic plagioclase. Several meteoritic phases were formed by shock metamorphism. Martensite (α₂-Fe,Ni) has a distorted body-centered-cubic structure and formed by a shear transformation from taenite during shock reheating and rapid cooling. The C polymorphs diamond, lonsdaleite and chaoite formed by shock from graphite. Suessite formed in the North Haig ureilite by reduction of Fe and Si (possibly from olivine) via reaction with carbonaceous matrix material. Ringwoodite, the spinel form of (Mg,Fe)₂SiO₄, and majorite, a polymorph of (Mg,Fe)SiO₃ with the garnet structure, formed inside shock veins in highly shocked ordinary chondrites. Secondary minerals in meteorite finds that formed during terrestrial weathering include oxides and hydroxides formed directly from metallic Fe-Ni by oxidation, phosphates formed by the alteration of schreibersite, and sulfates formed by alteration of troilite.     

Stratification and mixing of a post-glacial Neoproterozoic ocean: Evidence from carbon and sulfur isotopes in a cap dolostone from northwest China

To improve our knowledge about the geochemical and environmental aftermath of Neoproterozoic global glaciations, we analyzed stable isotopes (δ¹³C, δ¹⁸O, δ³⁴S) and elemental concentrations (Ca, Mg, S, Sr, Fe, and Mn) of the ～ 10-m-thick Zhamoketi cap dolostone atop the Tereeken diamictite in the Quruqtagh area, eastern Chinese Tianshan. Available chemostratigraphic data suggest that the Tereeken diamictite is probably equivalent to the Marinoan glaciation. Our new data indicate that organic and carbonate carbon isotopes of the Zhamoketi cap dolostone show little stratigraphic variations, averaging ? 28.2‰ and ? 4.6‰, respectively. In contrast, sulfur isotopes show significant stratigraphic variations. Carbonate associated sulfate (CAS) abundance decreases rapidly in the basal cap dolostone and δ³⁴S_CAS composition varies between + 9‰ and + 15‰ in the lower 2.5 m. In the overlying interval, CAS abundance remains low while δ³⁴S_CAS rises ～ 5‰ and varies more widely between + 10‰ and + 21‰. The range of δ³⁴S_py of the cap dolostone overlaps with that of δ³⁴S_CAS, but direct comparison shows that δ³⁴S_py is typically greater than δ³⁴S_CAS measured from the same samples. Hypotheses to explain the observations must account for both the remarkable sulfur isotope enrichment of pyrites and the inverse fractionation. We propose that CAS and pyrite were derived from two isotopically distinct reservoirs in a chemically stratified basin or a basin with a sulfate minimum zone. In this model, CAS was derived from shallow, oxic surface waters with moderate sulfate concentration and depleted in ³⁴S due to the post-glacial influx of sulfur from continental weathering. In contrast, pyrite was derived from anoxic bottom waters (or a sulfate minimum zone) with low sulfate concentration and ³⁴S enrichment due to long-term syn-glacial sulfate reduction. The rapid shift in CAS abundance and sulfur isotope composition within the cap dolostone is interpreted to reflect the mixing of the two reservoirs after initial deglaciation. Comparison with other post-Marinoan cap carbonates shows significant spatial heterogeneity in δ³⁴S_CAS, which together with strong temporal variation in δ³⁴S_CAS, points to generally low sulfate concentrations in post-Marinoan oceans.     

Oxygen isotope heterogeneity in chondrules from the Mokoia CV3 carbonaceous chondrite

We report a study of the oxygen isotope ratios of chondrules and their constituent mineral grains from the Mokoia, oxidized CV3 chondrite. Bulk oxygen isotope ratios of 23 individual chondrules were determined by laser ablation fluorination, and oxygen isotope ratios of individual grains, mostly olivine, were obtained in situ on polished mounts using secondary ion mass spectrometry (SIMS). Our results can be compared with data obtained previously for the oxidized CV3 chondrite, Allende. Bulk oxygen isotope ratios of Mokoia chondrules form an array on an oxygen three-isotope plot that is subparallel to, and slightly displaced from, the CCAM (carbonaceous chondrite anhydrous minerals) line. The best-fit line for all CV3 chondrite chondrules has a slope of 0.99, and is displaced significantly (by δ¹⁷O ∼ −2.5‰) from the Young and Russell slope-one line for unaltered calcium-aluminum-rich inclusion (CAI) minerals. Oxygen isotope ratios of many bulk CAIs also lie on the CV-chondrule line, which is the most relevant oxygen isotope array for most CV chondrite components. Bulk oxygen isotope ratios of most chondrules in Mokoia have δ¹⁸O values around 0‰, and olivine grains in these chondrules have similar oxygen isotope ratios to their bulk values. In general, it appears that chondrule mesostases have higher δ¹⁸O values than olivines in the same chondrules. Our bulk chondrule data spread to lower δ¹⁸O values than any ferromagnesian chondrules that have been measured previously. Two chondrules with the lowest bulk δ¹⁸O values (−7.5‰ and −11.7‰) contain olivine grains that display an extremely wide range of oxygen isotope ratios, down to δ¹⁷O, δ¹⁸O around -50‰ in one chondrule. In these chondrules, there are no apparent relict grains, and essentially no relationships between olivine compositions, which are homogeneous, and oxygen isotopic compositions of individual grains. Heterogeneity of oxygen isotope ratios within these chondrules may be the result of incorporation of relict grains from objects such as amoeboid olivine aggregates, followed by solid-state chemical diffusion without concomitant oxygen equilibration. Alternatively, oxygen isotope exchange between an ¹⁶O-rich precursor and an ¹⁶O-poor gas may have taken place during chondrule formation, and these chondrules may represent partially equilibrated systems in which isotopic heterogeneities became frozen into the crystallizing olivine grains. If this is the case, we can infer that the earliest nebular solids from which chondrules formed had δ¹⁷O and δ¹⁸O values around -50‰, similar to those observed in refractory inclusions.     

Impact melting in the Cumberland Falls and Mayo Belwa aubrites

Abstract– Six chondritic clasts in the Cumberland Falls polymict breccia were examined: four texturally resemble ordinary chondrites (OCs) and two are impact melt breccias containing shocked OC clasts adjacent to a melt matrix. The six chondritic clasts are probably remnants of a single OC projectile that was heterogeneously shocked when it collided with the Cumberland Falls host. Mayo Belwa is the first known aubrite impact melt breccia. It contains coarse enstatite grains exhibiting mosaic extinction; the enstatite grains are surrounded by a melt matrix composed of 3–16 μm‐size euhedral and subhedral enstatite grains embedded in sodic plagioclase. Numerous vugs, ranging from a few micrometers to a few millimeters in size, constitute ～5 vol% of the meteorite. They occur nearly exclusively within the Mayo Belwa matrix; literature data show that some vugs are lined with bundles of acicular grains of the amphibole fluor‐richterite. This phase has been reported previously in only two other enstatite meteorites (Abee and St. Sauveur), both of which are EH‐chondrite impact melt breccias. It seems likely that in Mayo Belwa, volatiles were vaporized during an impact event and formed bubbles in the melt. As the melt solidified, the bubbles became cavities; plagioclase and fluor‐richterite crystallized at the margins of these cavities via reaction of the melt with the vapor.     

Groundwater quality variations in glacial drift and bedrock aquifers,Barry County,Michigan, U.S.A.

Groundwater samples from 288 domestic wells in Barry County, Michigan, were analyzed for 33 inorganic chemical parameters. Variations in chemical composition were investigated by considering the possible effects of human impact, aquifer type (bedrock vs glacial drift), chemical evolution along groundwater flow paths, and glacial landform type (moraine vs outwash). Approximately 25 percent of the glacial drift wells were classified as degraded by human impact and were excluded from further analysis of chemical variation. Two-sample tests comparing individual concentrations from drift and bedrock aquifers suggest that groundwater in the Marshall Sandstone aquifer is derived from local recharge through the glacial drift. This conclusion is supported by generalized groundwater flow patterns recognized for the two aquifers.Concentrations in both aquifers were examined in relation to generalized flow paths derived from water level data and also by classification of wells as recharge, transition, and discharge. No spatial concentration trends in major ions were detected, although iron concentrations do appear to increase from recharge to discharge areas. Declining redox potential along groundwater flow paths may explain this trend.The possible influence of glacial landform type was investigated by comparing concentrations of wells in moraines with those in outwash deposits. Wells in moraines have significantly higher concentrations of most parameters, perhaps due to higher content of finer, more chemically reactive sediment grains.     

Flattened chondrules in the LAP 04581 LL5 chondrite: Evidence for an oblique impact into LL3 material and subsequent collisional heating

Abstract– LaPaz Icefield (LAP) 04581 is a shock‐stage S2 LL5 chondrite that initially consisted of unrecrystallized LL3 material with a moderately abundant fine‐grained porous matrix (on the order of 15 vol%). A rare oblique impact created shearing stresses that produced a petrofabric in the rock, induced frictional melting of troilite (thereby forming a large troilite vein), and caused chondrule flattening. The latter process was facilitated by impact‐induced collapse of matrix pores. Chondrule flattening could not have occurred if the rock had been impacted after it had been metamorphosed to type 5 levels because the fine‐grained matrix would have previously recrystallized and developed low porosity. Ar‐Ar dating of LAP 04581 yields an age of 4175 Ma. This date is long after ²⁶Al had decayed away and most likely reflects the timing of a second impact event that shocked the rock to S4–S5 levels. The troilite vein became polycrystalline at this time and the whole rock was annealed to petrologic type 5, perhaps by being buried beneath hot ejecta of low thermal diffusivity. After annealing, the rock was weakly shocked to S2 levels. LAP 04581 serves as an example of impact‐induced heating being a viable mechanism for chondrite metamorphism.     

Bioactive substances of various seaweeds and their applications and utilization

Over the past century or more,traditional uses of seaweeds began and initially comprised the simple collection,sorting and drying of seaweeds harvested from the wild,or cast upon the beach,for use as soil“manure/fertilizer/improver”.Some macroalgae were used for unprocessed food purposes and subsequently harvested and cultivated biomasses of selected brown and red seaweeds becameindustrially processed to yield alginates,mannitol,iodine,agar,agarose,carrageenan,and more recently biostimulants,etc.Products from various seaweeds are very diverse and are commonly applied in a range that includes textiles and dying,food/feed and supplements and specialized medical applications.