Carbonates in Vigarano: Terrestrial,preterrestrial, or both?

Abstract— Studies of two separate stones of the CV3 chondrite Vigarano have revealed the presence of previously unreported occurrences of calcite. In the first stone, calcite occurs as thin veins in a type B CAI. In contrast, observations of the second stone, which was recovered one month after its fall, show three calcite occurrences: networks of veins, vesicle fillings in the fusion crust, and pseudomorphic replacement of augite associated with a porphyritic olivine chondrule. The most common occurrence is as veins ranging in thickness from <1 μm to 25 μm and extending for more than several hundred μm. Some veins crosscut the fusion crust and are connected to a carbonate coating on the exterior of the meteorite. Extensive minor element zoning occurs in carbonate masses, indicating variations in the fluid composition and/or redox potential during carbonate growth. Based on the textural evidence and a comparative study with carbonate veins in the CV3 chondrite Leoville, we conclude that the veins are terrestrial in origin. We propose a model for rapid carbonate formation in which calcite precipitation is driven by hydrolysis and oxidation in the meteorite interior that move the fluid composition to alkaline values. In addition, both stones also contain minor occurrences of carbonate that are not readily explained by terrestrial alteration. Minor carbonate in a type B CAI occurs in the first stone and calcite occurs as pseudomorphic replacement of augite in the second stone. Both of these occurrences appear to be preterrestrial, probably asteroidal in origin.     

Root growth dynamics during recovery of tropical mountain forest in North-east India

Ever increasing pressures on tropical forests worldwide due to anthropogenic disturbances have greatly affected both above-and belowground functioning of these forests.While fine roots play major ecological roles in forests through assisting in nutrient and water uptake and returning elements to the soil environment,coarse roots play an important role in C sequestration.We studied changes in fine and coarse root biomass,production,turnover and carbon and nitrogen return to the soil in two regenerating forest stands(RFs)following stonemining that were 5 years(RF-5)and 15 years(RF-15)post-disturbance compared with a natural forest stand(NF)in Mizoram,North-east India.Fine(2mm)and coarse root(2-10 mm)biomass differed significantly among the forest stands and ranged from239(RF-5)to 415(NF)and 230(RF-5)to 436(NF)g m 2,respectively.Total root(fine+coarse)biomass increased during stand development but the proportion of very fine root(0.5 mm)to total root production decreased.Fine root biomass decreased with increasing soil depth.Fine and total root biomass showed strong seasonal correlations with soil moisture,more so than for rainfall and temperature,whereas these relationships were less clear for the coarse root biomass.The amount of N(25-55 kg ha~(-1))and C(1.9-3.6t ha~(-1))stored in root biomass increased with stand age with a corresponding increase in production and turnover of C and N to the soil.Disturbance to these tropical forests negatively affected root dynamics,influenced their spatiotemporal patterns,and reduced the production,amount and availability of nutrients returned to the soil along with a strong reduction in the root biomass carbon pool and sequestration in carbon residence time.We observed that root growth,especially fine roots,is dependent on abiotic variables,and plays a significant role in early stages of secondary succession by adding organic matter and nutrients through high turnover rates in these forests.     

The onset of metamorphism in ordinary and carbonaceous chondrites

Abstract— Ordinary and carbonaceous chondrites of the lowest petrologic types were surveyed by X‐ray mapping techniques. A variety of metamorphic effects were noted and subjected to detailed analysis using electron microprobe, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and cathodoluminescence (CL) methods. The distribution of Cr in FeO‐rich olivine systematically changes as metamorphism increases between type 3.0 and type 3.2. Igneous zoning patterns are replaced by complex ones and Cr‐rich coatings develop on all grains. Cr distributions in olivine are controlled by the exsolution of a Cr‐rich phase, probably chromite. Cr in olivine may have been partly present as tetrahedrally coordinated Cr³⁺. Separation of chromite is nearly complete by petrologic type 3.2. The abundance of chondrules showing an inhomogeneous distribution of alkalis in mesostasis also increases with petrologic type. TEM shows this to be the result of crystallization of albite. Residual glass compositions systematically change during metamorphism, becoming increasingly rich in K. Glass in type I chondrules also gains alkalis during metamorphism. Both types of chondrules were open to an exchange of alkalis with opaque matrix and other chondrules. The matrix in the least metamorphosed chondrites is rich in S and Na. The S is lost from the matrix at the earliest stages of metamorphism due to coalescence of minute grains. Progressive heating also results in the loss of sulfides from chondrule rims and increases sulfide abundances in coarse matrix assemblages as well as inside chondrules. Alkalis initially leave the matrix and enter chondrules during early metamorphism. Feldspar subsequently nucleates in the matrix and Na re‐enters from chondrules. These metamorphic trends can be used to refine classification schemes for chondrites. Cr distributions in olivine are a highly effective tool for assigning petrologic types to the most primitive meteorites and can be used to subdivide types 3.0 and 3.1 into types 3.00 through 3.15. On this basis, the most primitive ordinary chondrite known is Semarkona, although even this meteorite has experienced a small amount of metamorphism. Allan Hills (ALH) A77307 is the least metamorphosed CO chondrite and shares many properties with the ungrouped carbonaceous chondrite Acfer 094. Analytical problems are significant for glasses in type II chondrules, as Na is easily lost during microprobe analysis. As a result, existing schemes for chondrule classification that are based on the alkali content of glasses need to be revised.     

Dissolution Rates of Upper Mantle Minerals in an Alkali Basalt Melt at High Pressure: An Experimental Study and Implications for Ultramafic Xenolith Survival

The dissolution rates of the major upper mantle minerals olivine,orthopyroxene, clinopyroxene, spinel, and garnet have been determinedin an alkali basalt melt at superliquidus temperatures and 5,12, and 30 kb. At low pressure where olivine is the liquidusphase of the basalt, olivine has a slower dissolution rate thanclinopyroxene; however, at higher pressure where clinopyroxeneis the liquidus phase, clinopyroxene has a slower dissolutionrate than olivine. The relative rates of dissolution of olivineand clinopyroxene at each pressure are, therefore, governedby their relative stabilities in the melt and hence by the structureof the melt. As the degree of superheating above the liquidusincreases at each pressure, the dissolution rates of olivineand clinopyroxene converge, suggesting that the melt undergoestemperature-induced structural changes. Orthopyroxene has a dissolution rate similar to olivine at highpressure and similar to clinopyroxene at low pressure. Spinelhas the slowest dissolution rate at each pressure. Garnet dissolvesvery rapidly at 12 kb and at a comparable rate of olivine at30 kb. The dissolution rates determined in the experiments varyfrom 9.21 ? 10^–9cm s^–1 for spinel at 5 kbar and1250?C to 3.83 ? 10^–5cm s^–1 for garnet at 30 kband 1500?C. Textures produced during the dissolution experiments are relatedto mineral stability in the melt at each pressure and are independentof the degree of superheating. The mineral phases that are stableon or near the liquidus exhibit no reaction; whereas complexreaction textures and crystallization characterize dissolutionof minerals that are relatively unstable in the melt. Concentration profiles in the melt adjacent to the same crystalfor different experimental durations are identical, indicatingthat dissolution is time-independent and a steady-state process.However, cation diffusion coefficients calculated for single-componentoxides in the melt reveal that dissolution may not be completelycontrolled by diffusion of cations away from the crystal/meltinterface. The apparent diffusivities positively correlate withthe dissolution rate, which suggests that the stability of themineral is an important factor to consider when deriving diffusioncoefficients from these experiments. Other factors that maybe involved are multi-component effects and the nature of thediffusing species in the melt. A simple model has been constructed that predicts the survivalof ultramafic xenoliths in alkali basalt magmas as a functionof xenolith radius, magma ascent time and superheating. Theresults of the model suggest that the relative proportions ofperidotite and pyroxenite xenoliths brought to the surface inalkali basalts are generally representative of their proportionsas constituents of the upper mantle. Further experiments usingdifferent melt compositions are required to extend the model.     

Iron‐rich aureoles in the CM carbonaceous chondrites Murray,Murchison, and Allan Hills 81002: Evidence for in situ aqueous alteration

Abstract— Iron‐rich aureoles in CM carbonaceous chondrites are previously unidentified domains of aqueously altered matrix material, whose FeO content may exceed that of the surrounding matrix by up to more than 15 wt%. We describe the petrography and mineralogy of these objects in the CM chondrites Murray, Murchison, and Allan Hills (ALH) 81002. The size of Fe‐rich aureoles ranges from a few hundred microns to several millimeters in diameter and appears to be a function of the degree of alteration of the host chondrite. The origin of Fe‐rich aureoles is related to the alteration of large metal grains that has resulted in the formation of characteristic PCP‐rich reaction products that are frequently observed at the centers of the aureoles. This suggests that Fe‐rich aureoles in CM chondrites are the result of the mobilization of Fe from altering metal grains into the matrix. The fact that Fe‐rich aureoles enclose numerous chondritic components such as chondrules, calcium‐aluminum‐rich inclusions (CAIs), and mineral fragments, as well as their radial symmetric appearance, are strong evidence that they formed in situ and that significant directional fluid flow was not involved in the alteration process. This and additional constraints, such as the distribution of S and other elements, as well as the inferred alteration conditions, are consistent with in situ parent‐body alteration. The observations are, however, entirely incompatible with preaccretionary alteration models in which the individual CM chondrite components have experienced diverse alteration histories. The presence of numerous intact aureoles in the brecciated CM chondrites Murray and Murchison further suggests that the alteration occurred largely after brecciation affected these meteorites. Therefore, the progressive aqueous alteration of CM chondrites may not be necessarily coupled to brecciation as has been previously proposed.     

Characterization of micron‐sized Fe,Ni metal grains in fine‐grained rims in the Y‐791198 CM2 carbonaceous chondrite: Implications for asteroidal and preaccretionary models for aqueous alteration

Abstract— –The presence of apparently unaltered, micron‐sized Fe,Ni metal grains, juxtaposed against hydrated fine‐grained rim materials in the CM2 chondrite Yamato (Y‐) 791198 has been cited as unequivocal evidence of preaccretionary alteration. We have examined the occurrence, composition, and textural characteristics of 60 Fe,Ni metal grains located in fine‐grained rims in Y‐791198 using scanning electron microscopy (SEM) and electron microprobe analysis. In addition, three metal grains, prepared by focused ion beam (FIB) sample preparation techniques were studied by transmission electron microscopy (TEM). The metal grains are heterogeneously distributed within the rims. Electron microprobe analyses show that all the metal grains are kamacite with minor element contents (P, Cr, and Co) that lie either within or close to the range for other CM2 metal grains. X‐ray maps obtained by electron microprobe show S, P, and/or Ca enrichments on the outermost parts of many of the metal grains. Z‐contrast STEM imaging of FIB‐prepared Fe,Ni metal grains show the presence of a small amount of a lower Z secondary phase on the surface of the grains and within indentations on the grain surfaces. Energy‐filtered TEM (EFTEM) compositional mapping shows that these pits are enriched in oxygen and depleted in Fe relative to the metal. These observations are consistent with pitting corrosion of the metal on the edges of the grains and we suggest may be the result of the formation of Fe(OH)₂, a common oxidation product of Fe metal. The presence of such a layer could have inhibited further alteration of the metal grains. These findings are consistent with alteration by an alkaline fluid as suggested by Zolensky et al. (1989), but the location of this alteration remains unconstrained, because Y‐791198 was recovered from Antarctica and therefore may have experienced incipient terrestrial alteration. However, we infer that the extremely low degree of oxidation of the metal is inconsistent with weathering in Antarctica and that alteration in an extraterrestrial environment is more probable. Although the presence of unaltered or incipiently altered metal grains in these fine‐grained rims could be interpreted as evidence for preaccretionary alteration, we suggest an alternative model in which metal alteration was inhibited by alkaline fluids on the asteroidal parent body.     

Magnetite in ALH 84001: An origin by shock‐induced thermal decomposition of iron carbonate

Abstract— In martian orthopyroxenite ALH 84001, pockets of feldspathic glass frequently contain carbonate masses that have been disrupted and dispersed within feldspathic shock melt as a result of impact(s). Transmission electron microscope studies of carbonate fragments embedded within feldspathic glass show that the fragments contain myriad, nanometer‐sized magnetite particles with cuboid, irregular, and teardrop morphologies, frequently associated with voids. The fragments of carbonate must have been incorporated into the melt at temperatures of ?900°C, well above the upper thermal stability of siderite (FeCO₃), which decomposes to produce magnetite and CO₂ below ?450°C. These observations suggest that most, if not all, of the fine‐grained magnetite associated with Fe‐bearing carbonate in ALH 84001 could have been formed as result of the thermal decomposition of the siderite (FeCO₃) component of the carbonate and is not due to biological activity.     

Phyllosilicates in the matrix of the unique carbonaceous chondrite Lewis Cliff 85332 and possible implications for the aqueous alteration of CI chondrites

Abstract— The fine-grained matrix of the unique, unequilibrated carbonaceous chondrite Lewis Cliff (LEW) 85332 has been studied by scanning electron microscopy (SEM), electron probe microanalysis (EPMA) and transmission electron microscopy (TEM). Compositionally, LEW 85332 has a matrix that is more Fe-rich than typical CI chondrites but has elemental abundance ratios that appear to be closer to CI matrices than to CM or CR chondrites. The mineralogy of the matrix is dominated by phyllosilicate phases that are predominantly interlayered Fe-rich serpentine/saponite; anhydrous silicate phases such as olivine and pyroxene are rare. Minor magnetite, troilite and ferrihydrite also occur associated with the phyllosilicates. Despite the high degree of weathering in LEW 85332, the phyllosilicates appear to have an extraterrestrial origin, but the highly variable Mg/Fe ratios of saponite may be the result of partial terrestrial oxidation of Fe-rich saponite to a more Mg-rich saponite and ferrihydrite. Alternatively, some of the ferrihydrite may have formed as a result of terrestrial weathering of Fe-Ni metal. The compositional and mineralogical data suggest that the matrix of LEW 85332 may represent a very early stage in the type of aqueous alteration experienced by the CI chondrites, although it is improbable that LEW 85332 was a precursor to the CI chondrites because of its high abundance of chondrules. The absence of carbonates, the high-Fe content of the matrix and phyllosilicate phases and relatively low abundance of magnetite all indicate that the degree of oxidation and leaching of LEW 85332 matrix was significantly less than that experienced by the CI chondrites. The absence of clear evidence for alteration of chondrules suggests that either the formation of the hydrous phases in the matrix occurred prior to accretion or that alteration occurred on a parent body and involved limited amounts of fluid, such that the reactions took place preferentially and exclusively within the fine-grained (anhydrous?) matrix materials.     

Origin and mechanical significance of honeycomb garnet in high-pressure metasedimentary rocks from the Tauern Window, Eastern Alps

High-pressure schists (2–2.5 GPa) from the Eclogite Zone in the Tauern Window contain honeycomb garnet in which fine webs of garnet surround strain-free quartz ± carbonate grains. High-resolution X-ray computed tomography shows that the garnet webs form a cellular structure that coats all surfaces of the inclusions. Electron backscatter diffraction analysis shows that the garnet cells are crystallographically continuous with more massive garnet regions, and that the quartz ± carbonate inclusions have random orientations; in contrast, matrix quartz exhibits a prominent crystallographic preferred orientation (CPO). High-resolution transmission electron microscopy shows few dislocations in either the garnet or the inclusion quartz. Most honeycomb garnet is chemically homogeneous, but some displays asymmetric core–rim zoning. Taken together, these observations are most consistent with formation of the garnet sheets via precipitation from a wetting fluid along quartz–quartz grain boundaries, or possibly via wholesale precipitation of garnet + quartz ± carbonate from a fluid. In either case, a silicate-rich aqueous fluid must have been present. The likelihood that a fully wetting fluid existed at high pressure has important implications for rheology during subduction of metasedimentary rocks: strain may be accommodated by grain rotation and sliding in an aqueous silicate slurry, rather than via dislocation creep mechanisms at high pressures. The absence of a CPO in early quartz may thus point to involvement of a pervasive grain-boundary fluid rather than requiring low differential stresses during subduction.     

Deciphering the nebular and asteroidal record of silicates and organic material in the matrix of the reduced CV3 chondrite Vigarano

We have conducted scanning electron microscope (SEM) and transmission electron microscope (TEM) studies of a variety of occurrences of matrix in the reduced CV3 chondrite breccia Vigarano. Matrix, which occurs as clastic interchondrule material and finer‐grained rims, is dominated by morphologically variable olivines that host submicron, hercynitic spinel, and carbonaceous inclusions. Clastic matrix and fine‐grained rims show significant differences in their olivine morphologies, abundance, and composition of olivine inclusions, and characteristics of the carbonaceous matter. We suggest that these differences are the result of different degrees of alteration of clastic matrix and rims and are not due to variability in their precursor materials. Textural and compositional characteristics of olivine in the matrix are consistent with formation by growth, possibly from an amorphous precursor material during asteroidal metamorphism, in the presence of limited quantities of aqueous fluids. Spinel inclusions in olivine may be nebular condensates that acted as seeds for nucleation of olivine or may have formed during metamorphism and were subsequently overgrown by olivine. Carbonaceous material occurs as nanometer‐sized inclusions within olivine in both fine‐grained rims and clastic matrix, but is most abundant as 100–200 nm grains, interstitial to matrix olivines. Most carbonaceous material is amorphous, but poorly graphitized carbon (PGC) also occurs as a minor component in both olivine inclusions and interstitial C. The widespread occurrence of fine‐grained amorphous carbon grains in the interstitial regions between olivine grains may preserve the distribution and grain size of nebular organic material. No clear textural relationships exist between carbonaceous grains and the other mineralogical components of Vigarano matrix that could help constrain the origin of the organic grains (i.e., evidence for Fischer‐Tropsch‐type reactions). Finally, there are considerable differences between matrix olivines in Vigarano in comparison with those in oxidized CV3 chondrites. In particular, the mineralogy and morphology of the matrix olivines and the nature, composition, and distribution of inclusions in the olivine grains are distinct. Based on these differences, we conclude that matrix in the oxidized CV3 chondrites could not have formed by thermal processing of Vigarano‐like material.