Mineralogy and petrology of silicate inclusions in iron meteorites

Silicate inclusions in 17 iron meteorites have been analyzed by the electron microprobe and classified, according to their phase assemblages, compositions, and textures, into three major types: Odessa, Copiapo, and Weekeroo Station, and three miscellaneous types: Enon, Kendall County, and Netschaëvo. Phase compositions in both Odessa- and Copiapo-type inclusions are very similar, but the two types are different in texture and constituent phases. Weekeroo Station-type inclusions are very different in every respect from other inclusions.For Odessa- and Copiapo-type inclusions, the distribution coefficients of Fe²⁺ and Mg in coexisting orthopyroxene and clinopyroxene indicate equilibration temperatures of 1,000° C, and the Ca/(Ca+Mg) ratios indicate temperatures of 900° C to 1,000° C. Equilibration temperatures determined for chromite-olivine pairs have a higher range of 1,154° C to 1,335° C. Minor element distributions among coexisting ferromagnesian silicates in these inclusions follow consistent patterns and are constant for any given sample, suggesting equilibrium assemblages. Major and minor element distributions for Weekeroo Station inclusions are anomalous, indicating nonequilibrium.Compositional data, the fragmentary shapes of many inclusions, the highly differentiated characteristic of two types of inclusions, the apparent disequilibrium between kamacite in inclusions and kamacite of the iron host, and the relict chondrules found in Netschaëvo suggest that many of the inclusions did not form cogenetically with the iron host, but represent pre-existing stony material that was taken up by an iron melt, probably not in the core of the parent body (or bodies).     

Clast sizes of ejecta from explosive eruptions on asteroids: implications for the fate of the basaltic products of differentiation

We use a simple model of the formation, growth, coalescence and migration of veins of basaltic melt generated by partial melting in chondritic asteroids to deduce the sizes of, and pressures within, the fluid-filled dikes reaching the surfaces of such bodies. The gas contents ( 1000 ppm of mainly CO and N₂) of the asteroids were high enough that bubbles of free gas trapped in the melt veins gave the basaltic melts significant buoyancy; expansion of these gases as a dike opened to the vacuum at the surface led to fragmentation of the melts into liquid droplets which were transported upwards by the accelerating gases to the surface. The sizes of these droplets and, hence, of the pyroclastic glass beads into which they cooled, are calculated to lie in the range 30 μm to 4 mm; this range is essentially independent of the size or gas content of the asteroid parent and only weakly dependent on the internal pressure of the erupting fluid. The fate of the pyroclasts, however, does depend on all of these factors. At very low internal pressures, significant separation of the gas and liquid in a rising dike may take place and not all of the liquid will be expelled from the dike when it opens to the surface. For relatively large ( 100 km radius) asteroids with relatively low ( 300 ppm) gas contents, the larger clasts are too heavy to be lifted from the level at which magma fragmentation takes place by the gas flow and so would also remain behind to form basaltic veins. The apparent absence of basaltic veins in meteorites then implies both that internal pressures in near-surface dikes were generally greater than 0.3 MPa and that low gas contents were not common. Finally, as long as pyroclasts are lofted from the magma fragmentation level, they will be accelerated to at least 90% of the final gas speed. If this speed exceeds the escape speed from the asteroid (as happens readily for high gas contents and small asteroids), the pyroclasts will be expelled into space and lost from the meteorite record. Otherwise (low gas contents or large asteroids), they will eventually fall back to be incorporated into the surface regolith, modifying the chemical and physical properties of meteorites subsequently derived from it.     

Matrix material in type 3 chondrites—occurrence,heterogeneity and relationship with chondrules

Matrix material in type 3 chondrites forms rims on chondrules, metal-sulfide aggregates, Ca,Al-rich inclusions and chondritic clasts; it also forms lumps up to a millimeter in size, which may contain coarser silicates. Chondrules of all types were found with internal matrix lumps that appear to have entered the chondrules before the latter had crystallized. Mean concentrations of Mg, Na, Al and Ca in matrix occurrences show up to fivefold variations in a single chondrite. Variations between mean matrix compositions of individual type 3 ordinary chondrites are almost as large and partly reflect systematic differences between H, L and LL matrices. Such variations are probably a result of nebular separation of feldspathic material and ferromagnesian silicates.Compositions of chondrules and their matrix rims are normally unrelated, although rim compositions are correlated with those of matrix lumps inside chondrules. A single chondrule was found with a composition nearly identical to that of its internal matrix lump, suggesting that some chondrules may have formed from matrix material. Matrix lumps are as heterogeneous as chondrules, but mean chondrule and matrix compositions differ, even allowing for possible loss of metallic Fe,Ni during chondrule formation. Since bulk compositions of matrix lumps and rims have probably not changed significantly since their formation except for Fe-Mg exchange, our matrix samples cannot represent typical chondrule precursor materials.     

SIZE-DISTRIBUTIONS OF CHONDRULE TYPES IN THE INMAN AND ALLAN HILLS A77011 L3 CHONDRITES

A petrographc study of 9 thin sections of Inman (L3) and 18 thin sections of ALHA77011 (L3) served to determine the size-distributions of different chondrule textural types. Inman chondrules are significantly larger than those in ALHA77011, but in each chondrite, there is no statistically significant difference between the size-distributions of barred olivine and radial pyroxene plus cryptocrystalline chondrules. In ALHA77011, barred olivine chondrules outnumber radial pyroxene plus cryptocrystalline chondrules, whereas in Inman, the reverse is true. Because compound and cratered chondrules were formed by the collision of similarly-sized objects, the dustball precursors of chondrules must have been size-sorted prior to chondrule formation. The region of dustball size-sorting in the solar nebula must have been very large, similarly affecting the physically-separated precursors of different chondrule types. Size-sorting was probably accomplished by aerodynamic particle-gas interactions. Zones of dustball melting (i.e., chondrule formation) were relatively small, generally affecting only dustballs of one compositional type and relatively uniform size. Different chondrule types were then mixed together in somewhat variable ratios. Within the region where chondrites of a particular compositional group agglomerated, there were sub-reservoirs that contained (roughly) uniformly large or uniformly small chondrules with different mixtures of textural types.     

THE ORO GRANDE,NEW MEXICO,CHONDRITE AND ITS LITHIC INCLUSION

The Oro Grande, New Mexico, U.S.A., chondrite was found in 1971. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 19.3 mole percent), orthopyroxene (Fs 16.2 mole percent), diopside, feldspar (An 13.6 mole percent), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. A bulk chemical analysis of the meteorite shows the following results (weight percent): Fe 0.84, Ni 1.46, Co 0.07, FeS 3.62, SiO₂ 34.18, TiO₂ 0.14, Al₂O₃ 1.83, Cr₂O₃ 0.55, Fe₂O₃ 21.25, FeO 9.13, MnO 0.31, MgO 21.52, CaO 1.72, Na₂O 0.70, K₂O 0.08, P₂O₅ 0.25, H₂O+ 2.14, H₂O^- 0.40, C 0.22, Sum 100.41. On the basis of composition and texture, the Oro Grande meteorite is classified as an H5 chondrite. A large lithic fragment (～5 mm long) with a very fine-grained texture different from that of the host meteorite was analyzed for bulk composition using the broad beam of an electron microprobe, and was found to be enriched in Ca, Al, Na, and K, and depleted in Mg and Fe relative to the bulk composition of the host meteorite. Its mineral compositions, however, are very similar to those of the host. It is suggested that the fragment is not a xenolith of a previously undescribed type of achondrite, but is probably an impact-produced partial melt of the host chondrite or a fragment of an unusually large chondrule.     

Mechanisms of pore water organic matter adsorption to montmorillonite

The extent and mechanisms of adsorption of marine pore water organic matter to montmorillonite were studied in a series of batch and sequential adsorption experiments. Pore water natural organic matter (pNOM) and easily extracted natural organic matter (eNOM) were collected from Liberty Bay (Puget Sound, WA, USA) sediments. The pNOM and eNOM were each divided into two size fractions using a 1000 D ultrafilter. Batch adsorption isotherms were approximately linear, and the >1000 D fractions of both pNOM and eNOM had larger partition coefficients (K_d) than the <1000 D fractions. A two-component fit of the sequential adsorption data indicated that pNOM and eNOM contained a similar amount of NOM (30%) that was not surface reactive toward montmorillonite. After correcting the batch adsorption K_ds for the non-reactive components, the K_ds estimated by batch and sequential adsorption were identical (2.7 l/kg for >1000 D pNOM and eNOM, and 1.6 l/kg for <1000 D pNOM and eNOM). Mechanisms of adsorption were investigated by systematically changing conditions (pH, temperature and ionic composition) of >1000 D fractions during batch isotherm experiments. Adsorption of NOM was found to decrease with increased temperature, suggesting that hydrophobic effects were not the dominant adsorption mechanisms in this system. Ion exchange was also not an important adsorption mechanism because adsorption increased with ionic strength. The observed enhancement in adsorption with ionic strength indicated that van der Waals interactions were important in the adsorption of NOM. Ligand exchange was found to be a significant mechanism since the presence of SO₄²⁻ in solution reduced the amount of NOM adsorbed. Ca²⁺ enhanced adsorption slightly more than Na⁺, suggesting that cation bridging was involved. The relative contributions of van der Waals interactions, ligand exchange and cation bridging were estimated to be approximately 60%, 35% and 5%, respectively, for adsorption of NOM in a CaCl₂ solution.     

IMPLICATIONS OF POIKILITIC TEXTURES IN LL-GROUP CHONDRITES

Lithic fragments in LL-group chondrites commonly have poikilitic textures, in part or in whole, where mainly olivine is enclosed by orthopyroxene. Partially poikilitic fragments also have grano-blastic areas and anhedral olivine larger than the olivine enclosed by pyroxene. In analogy to lunar poikilitic rocks and lithic fragments, poikilitic lithic fragments in LL-group chondrites, i.e., meteorites which are highly brecciated due to repeated impacts, are also interpreted as being related to impact events on meteorite parent bodies where melting and reheating of protolith occurred. Compositional characteristics of minerals in certain fragments, such as highly-unequilibrated clinopyroxene (CaO, 14.5 to 17.3 wt %; Al₂O₃, 6.7%) and relatively high CaO (0.70 to 2.5 wt %) in orthopyroxene in a Ngawi fragment, seem to indicate a melt origin. However, as in the lunar case, it is difficult to decide whether the meteoritic poikilitic textures resulted from complete or partial melting or largely by solid-state recrystallization, although the large olivines that may be relict crystals appear to indicate that at least partial melting was involved. In all probability, all three processes are responsible for the poikilitic textures in chondrites, since temperature regimes produced by impact processes are likely to range widely. These interpretations may also apply to the poikilitic-textured Shaw chondrite, L-group, which may owe its poikilitic texture to impact partial-melting processes while in the parent body regolith.     

The empty shell of the planetary: re-rooting the urban in the experience of the urbanites

ABSTRACT

This paper offers reflections on a body of work that has been produced under the label of “planetary urbanization”. This term has its roots in speculative work by French writer Henri Lefebvre in the late 1960s and early 1970s and has recently been popularized by a new generation of critical urban theorists. In this commentary, I propose that Lefebvre’s idea of planetary urbanization (and the aligned concepts “complete urbanization” and “urban society”) offer a way to think productively about post-capitalist possibilities. Making reference to early writings by Marx and Engels about communism and the end of human pre-history, I argue that planetary urbanization presents a terrain for liberation from the constraints of capitalist histories. Given that this terrain is currently defined by the domains of neoliberalism and climate change a new politics is necessary to unlock the possibilities of urban society.     

Recent Publications

The government of Ontario, Canada, has passed legislation to protect large parts of the southern portions of the province from most development. An extensive plan for a Greenbelt that surrounds the Greater Toronto Area and other regional growth centers was introduced. This article looks at the new policy as a spatial strategy that shifts the scales of environmental and growth management policy in Ontario. The legislation also sets the framework for a state spatial project; that is, a set of changes in how the regional state internally operates. The current Greenbelt legislation is a new step in a longer term development by which governments in Ontario have attempted to regulate the relationships between cities and regions, town and hinterland. Overlapping strongly with what is usually called the Toronto bioregion between the Niagara Escarpment, Oak Ridges Moraine, and Lake Ontario, the Greenbelt reorganizes space in southern Ontario in ways that would further ecosystem policies and practices in the area. Theoretically guided by newer debates on rescaling and regionalism, and based on close reading of the planning and policy documents on the Greenbelt as well as a series of expert interviews, we argue that the current Greenbelt legislation is an act of up-scaling traditional urban-regional regulation in southern Ontario, which we shall call extended metropolitanization. Such rescaling recasts traditional political conflicts in new terms. We conclude that extended metropolitanization in southern Ontario has been a process that has brought nature, the state, and governance together into a new regional sustainability fix.