Diamond formation and source carbonation: mineral associations in diamonds from Namibia

Mineral inclusions in diamonds from Namibia document a range of mantle sources, including eclogitic, websteritic and peridotitic parageneses. Based on unusual textural features a group of inclusions showing websteritic, peridotitic and transitional chemical features is assigned to an 'undetermined suite' (12% of the studied diamonds). The mutual characteristic of this group is the occurrence of lamellar intergrowths of clinopyroxene and orthopyroxene. In addition, the 'undetermined suite' is associated with a number of uncommon phases: in one diamond MgCO₃ is enclosed by clinopyroxene. Other minerals that form touching inclusions with the pyroxene lamellae are (1) a SiO₂ phase observed in three diamonds, together with CaCO₃ in one of them, (2) phlogopite and a Cr-rich 'titanate' (probably lindsleyite). The inclusions document a metamorphic path of decreasing pressures and temperatures after entrapment in diamond. First, homogeneous low-Ca clinopyroxenes were entrapped at high temperatures. They subsequently exsolved orthopyroxene and probably also SiO₂ (coesite) on cooling along a P,T trajectory that did not allow garnet to be exsolved as well. Phlogopite, carbonates and LIMA phases are the result of overprint of a peridotitic source rock by a carbon-rich agent. The resulting unusual, olivine-free mineral association and the host diamonds are interpreted as products of extensive carbonation of the peridotite.     

Argon retention properties of silicate glasses and implications for <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar age and noble gas diffusion studies

Sized aggregates of glasses (47–84 wt% SiO₂) were fused from igneous-derived cohesive fault rock and igneous rock, and step-heated from ~400 to >1,200 °C to obtain their ³⁹Ar diffusion properties (average E=33,400 cal mol^?1; D _o=4.63×10^?3 cm² s^?1). At T<~1,000 °C, glasses containing <~69 wt% SiO₂ and abundant network-forming cations (Ca, Fe, Mg) reveal moderate to strong non-linear increases in D and E, reflecting structural modifications as the solid transitions to melt. Extrapolation of these Arrhenius properties down to typical geologic T-t conditions could result in a 1.5 log₁₀ unit underestimation in the diffusion rate of Ar in similar materials. Numerical simulations based upon the diffusion results caution that some common geologic glasses will likely yield ⁴⁰Ar/³⁹Ar cooling ages rather than formation ages. However, if cooling rates are sufficiently high, ambient temperatures are sufficiently low (e.g., <65–175 °C), and coarse particles (e.g., radius (r) >~1 mm) are analyzed, glasses with compositions similar to ours may preserve their formation ages.     

A technique to improve the empirical mode decomposition in the Hilbert-Huang transform

The Hilbert-based time-frequency analysis has promising capacity to reveal the time-variant behaviors of a system. To admit well-behaved Hilbert transforms, component decomposition of signals must be performed beforehand. This was first systematically implemented by the empirical mode decomposition (EMD) in the Hilbert-Huang transform, which can provide a time-frequency representation of the signals. The EMD, however, has limitations in distinguishing different components in narrowband signals commonly found in free-decay vibration signals. In this study, a technique for decomposing components in narrowband signals based on waves’ beating phenomena is proposed to improve the EMD, in which the time scale structure of the signal is unveiled by the Hilbert transform as a result of wave beating, the order of component extraction is reversed from that in the EMD and the end effect is confined. The proposed technique is verified by performing the component decomposition of a simulated signal and a free decay signal actually measured in an instrumented bridge structure. In addition, the adaptability of the technique to time-variant dynamic systems is demonstrated with a simulated time-variant MDOF system.     

An evaluation of the role played by remote sensing technology following the World Trade Center attack

Remote sensing technology has been widely recognized for contributing to emergency response efforts after the World Trade Center attack on September 11th, 2001. The need to coordinate activities in the midst of a dense, yet relatively small area, made the combination of imagery and mapped data strategically useful. This paper reviews the role played by aerial photography, satellite imagery, and LIDAR data at Ground Zero. It examines how emergency managers utilized these datasets, and identifies significant problems that were encountered. It goes on to explore additional ways in which imagery could have been used, while presenting recommendations for more effective use in future disasters and Homeland Security applications. To plan adequately for future events, it was important to capture knowledge from individuals who responded to the World Trade Center attack. In recognition, interviews with key emergency management and geographic information system (GIS) personnel provide the basis of this paper. Successful techniques should not be forgotten, or serious problems dismissed. Although widely used after September 11th, it is important to recognize that with better planning, remote sensing and GIS could have played an even greater role. Together with a data acquisition timeline, an expanded discussion of these issues is available in the MCEER/NSF report “Emergency Response in the Wake of the World Trade Center Attack; The Remote Sensing Perspective” (Huyck and Adams, 2002)     

Hornblende-dehydration melting in mafic rocks and the link between massif-type charnockite and associated granulites,Eastern Ghats Granulite Belt,India

A massif-type (intrusive) charnockite body in the Eastern Ghats granulite belt, India, is associated with hornblende-bearing mafic granulite, two-pyroxene granulite and enderbitic granulite. The charnockite is characterised by pervasive gneissic foliation (S₁). This is axial planar to the folded layers of hornblende-bearing mafic granulite (F₁ folds), indicating that the granulite protoliths were present before the development of S₁. Two-pyroxene granulite and enderbitic granulite occur as lenticular patches disposed along the foliation and hence could be syngenetic to S₁. The tonalitic to granodioritic, metaluminous to weakly peraluminous compositions and relatively high Sr/Rb of the charnockite are consistent with its derivation by partial melting of a mafic protolith. Strong Y depletion, lack of Sr depletion and strongly fractionated REE patterns with high (La/Yb)_N ratio, but relatively lower HREE (Gd/Lu) fractionation with marked positive Eu anomalies, suggest major residual hornblende (as well as garnet), but not plagioclase, consistent with the hornblende dehydration melting in the source rocks. Such a residual mineralogy is broadly similar to those of some of the hornblende-bearing mafic granulite inclusions, which have compositional features indicative of a restitic nature. Quantitative modelling supports an origin for the charnockite melts by partial melting of a hornblende-rich mafic granulite source, although source heterogeneity is very likely given the rather variable trace element contents of the charnockite. The whole-rock and mineral compositions of the two-pyroxene granulites and enderbitic granulites are consistent with them representing peritectic phase segregations of hornblende-dehydration melting. A clockwise P-T path implies that melting could have occurred in thickened continental crust undergoing decompression.Editorial responsibility: T.L. Grove     

Enthalpies in (Na,Ca)- and (K,Ca)-feldspar binaries: a high-temperature solution calorimetric study

A series of high structural state plagioclases (Ab-An) was crystallized from glasses. By exchanging Na for K in KCl melts, metastable K-plagioclases (Or-An) were prepared which possess the same structural state as the starting plagioclases. Both series were investigated at 980 K by lead borate solution calorimetry. Continuing the ideas of Carpenter and McConnell (1984) and Carpenter (1992a), the results can be interpreted as follows. In the high plagioclase series, the enthalpies of solution, jH_sol, reflect the schemes of Al,Si ordering: (1) analbite-like (C2/m) ordering in the An-poor region 0hX_AnА.2, (2) high albite-like (C1¥) ordering in intermediate plagioclases, and (3) anorthite-like (I1¥) ordering in the An-rich region 0.7AnБ. In regions 1 and 2, jH_sol decreases as a function of X_An, but increases in region 3 as a consequence of the C1¥MI1¥ ordering reaction. Therefore, it is not a mixing effect but a compositionally restricted ordering effect which causes the excess enthalpies, jH^ex, to be positive in the plagioclase binary as a whole. Neglecting the existence of phase transitions at X_An=0.2 and X_An=0.7, jH^ex can be approximated by a two-parameter Margules model yielding W^H_AnAb=14Dž kJ/mol and W^H_AbAn=40Dž kJ/mol. jH_sol values of I1¥ plagioclases (X_An>0.7) can be "corrected" for the C1¥MI1¥ ordering effect (Carpenter 1992a). When combining the corrected values with the jH_sol data which were actually measured on the C1¥ plagioclases (X_An<0.7), negative excess enthalpies are generated in the plagioclase binary. This may be expected when C1¥ ordering occurs relative to topochemically monoclinic reference states of analbite and hypothetical anorthite devoid of I1¥ order. The solution experiments on the K-plagioclases resulted in similar characteristics as those found for the plagioclases. However, in addition to the ordering effects observed in the plagioclase binary, volume mismatch effects contribute to jH^ex in the K-plagioclase series. jH^ex can be represented by a Margules model with W^H_AnOr=60ᆞ kJ/mol and W^H_OrAn=91ᆢ kJ/mol when the phase transitions at X_An=0.2 and X_An=0.7 are again neglected. The contribution of the volume mismatch effect to jH^ex is considerable, as appears from the large difference between the K-plagioclase and the plagioclase Margules parameters. Their difference corresponds to a practically symmetrical dependence of jH^ex_volmism on composition, with W^H_volmism=48ᆡ kJ/mol.     

Absarokites from the western Mexican Volcanic Belt: constraints on mantle wedge conditions

We have investigated the near liquidus phase relations of a primitive absarokite from the Mascota region in western Mexico. Sample M.102 contains ~11.6 wt% MgO, Mg#=0.73 and the lava contains Fo₉₀ olivine phenocrysts, indicating near equilibrium with the mantle. High-pressure experiments on a synthetic analogue of the absarokite composition containing low and high H₂O abundances of (~2 and ~5 wt%, respectively) were performed in a piston cylinder apparatus over the pressure range of 1.2 to 2.0 GPa. The composition containing ~2 wt% H₂O is multiply saturated with olivine and orthopyroxene at 1.6 GPa and 1,400 °C. At the same pressure, clinopyroxene appears 30 °C below the liquidus. At an H₂O content of ~5 wt% the multiple saturation with olivine and orthopyroxene occurs at 1.7 GPa and 1,300 °C. Assuming a batch-melting process, we suggest that the primitive absarokite was segregated from a depleted lherzolite or harzburgite residue at ~50 km, placing the depth of origin well within the mantle wedge beneath the Jalisco Block. A low degree (<5 %wt%) batch-melt of an original metasomatized depleted lherzolite or harzburgite source would contain the observed trace element abundances found in M.102. The liquidus phase relations are not consistent with the presence of non-peridotitic veins at the depth of last equilibration. Therefore, we propose that the Mascota absarokites segregated at an apparent melt fraction of less than 5% from a depleted peridotitic source. Melting first began at a greater depth as a small degree H₂O- and trace element- rich melt of a metasomatized peridotite that ascended into the overlying wedge and re-equilibrated with shallower, hotter mantle.Editorial responsibility: J. Hoefs     

Adakite-like signature of Late Miocene intrusions at the Los Pelambres giant porphyry copper deposit in the Andes of central Chile: metallogenic implications

Adakite-like features are recognized in the Late Miocene (~10 Ma) porphyritic intrusions of the Los Pelambres giant porphyry copper deposit, central Chile (32°S). Located within the southern portion of the flat-slab segment (28–33°S) of the Chilean Andes, the Al- and Na-rich porphyries of Los Pelambres display distinctly higher Sr/Y (~100–300) and La_N/Yb_N (~25–60) ratios than contemporaneous and barren magmatic units (e.g., La Gloria pluton, Cerro Aconcagua volcanic rocks) of the same Andean magmatic belt. Strong fractionation of heavy rare earth elements (HREE), absence of Eu anomalies, high Sr/Y and Zr/Sm and low Nb/Ta ratios suggest melt extraction from a garnet-amphibolite source. The Late-Miocene adakite-like porphyritic intrusions at Los Pelambres formed closely related in time and space to the subduction of the Juan Fernández Ridge (JFR) hotspot chain along the Chilean margin. Current tectonic reconstructions reveal that, at the time of formation of the Los Pelambres rocks, a W-E segment of the JFR started to subduct beneath them, producing a slow-down of a previously rapid southward migration of a NE-ridge—trench collision. These particular tectonic conditions are favorable for the origin of the Los Pelambres porphyry suite by melting of subducting young hotspot rocks under flat-slab conditions. The incorporation of crustal components into the oceanic lithopheric magma source by subduction erosion is evidenced by the Sr-Nd isotope composition of the Los Pelambres rocks different from the MORB signatures of true adakites. A close relationship apparently exists between the origin of this adakite-like magmatism and the source of the mineralization in the Los Pelambres porphyry copper deposit.Editorial handling: R.J. Goldfarb     

Stable isotope (C,O, S) systematics of the mercury mineralization at Idrija,Slovenia: constraints on fluid source and alteration processes

The world-class Idrija mercury deposit (western Slovenia) is hosted by highly deformed Permocarboniferous to Middle Triassic sedimentary rocks within a complex tectonic structure at the transition between the External Dinarides and the Southern Alps. Concordant and discordant mineralization formed concomitant with Middle Triassic bimodal volcanism in an aborted rift. A multiple isotopic (C, O, S) investigation of host rocks and ore minerals was performed to put constraints on the source and composition of the fluid, and the hydrothermal alteration. The distributions of the ¹³C and ¹⁸O values of host and gangue carbonates are indicative of a fracture-controlled hydrothermal system, with locally high fluid-rock ratios. Quantitative modeling of the ¹³C and ¹⁸O covariation for host carbonates during temperature dependent fluid-rock interaction, and concomitant precipitation of void-filling dolomites points to a slightly acidic hydrothermal fluid (¹³C–4 and ¹⁸O+10), which most likely evolved during isotopic exchange with carbonates under low fluid/rock ratios. The ³⁴S values of hydrothermal and sedimentary sulfur minerals were used to re-evaluate the previously proposed magmatic and evaporitic sulfur sources for the mineralization, and to assess the importance of other possible sulfur sources such as the contemporaneous seawater sulfate, sedimentary pyrite, and organic sulfur compounds. The ³⁴S values of the sulfides show a large variation at deposit down to hand-specimen scale. They range for cinnabar and pyrite from –19.1 to +22.8, and from –22.4 to +59.6, respectively, suggesting mixing of sulfur from different sources. The peak of ³⁴S values of cinnabar and pyrite close to 0 is compatible with ore sulfur derived dominantly from a magmatic fluid and/or from hydrothermal leaching of basement rocks. The similar stratigraphic trends of the ³⁴S values of both cinnabar and pyrite suggest a minor contribution of sedimentary sulfur (pyrite and organic sulfur) to the ore formation. Some of the positive ³⁴S values are probably derived from thermochemical reduction of evaporitic and contemporaneous seawater sulfates.Editorial handling: P. Lattanzi     

Composite synvolcanic intrusions associated with Precambrian VMS-related hydrothermal systems

Large subvolcanic intrusions are recognized within most Precambrian VMS camps. Of these, 80% are quartz diorite–tonalite–trondhjemite composite intrusions. The VMS camps spatially associated with composite intrusions account for >90% of the aggregate sulfide tonnage of all the Precambrian, intrusion-related VMS camps. These low-alumina, low-K, and high-Na composite intrusions contain early phases of quartz diorite and tonalite, followed by more voluminous trondhjemite. They have a high proportion of high silica (>74% SiO ₂) trondhjemite which is compositionally similar to the VMS-hosting rhyolites within the volcanic host-rock successions. The quartz-diorite and possibly tonalite phases follow tholeiitic fractionation trends whereas the trondhjemites fall within the composition field for primitive crustal melts. These transitional M-I-type primitive intrusive suites are associated with extensional regimes within oceanic-arc environments. Subvolcanic composite intrusions related to the Archean Sturgeon Lake and Noranda, and Paleoproterozoic Snow Lake VMS camps range in volume from 300 to 1,000 km ³. Three have a sill morphology with strike lengths between 15 and 22 km and an average thickness between 1,500 and 2,000 m. The fourth has a gross stock-like shape. The VMS deposits are principally restricted to the volcanic strata above the strike length of the intrusions, as are areally extensive, thin exhalite units. The composite intrusions contain numerous internal phases which are commonly clustered within certain parts of the composite intrusion. These clusters underlie eruptive centers surrounded by areas of hydrothermal alteration and which contain most of the VMS deposits. Early quartz-diorite and tonalite phases appear to have intruded in rapid succession. Evidence includes gradational contacts, magma mixing and disequilibrium textures. They appear to have been emplaced as sill-dike swarms. These early phases are present as pendants and xenoliths within later trondhjemite phases. The trondhjemite phases contain numerous internal contacts indicating emplacement as composite sills. Common structural features of the composite intrusions include early xenolith phases, abundant small comagmatic dikes, fractures and veins and, in places, columnar jointing. Internal phases may differ greatly in texture from fine- to coarse-grained, aphyric and granophyric through seriate to porphyritic. Mineralogical and isotopic evidence indicates that early phases of each composite intrusion are affected by pervasive to fracture-controlled high-temperature (350–450 °C) alteration reflecting seawater-rock interaction. Trondhjemite phases contain hydrothermal-magmatic alteration assemblages within miarolitic cavities, hydrothermal breccias and veins. This hydrothermal-magmatic alteration may, in part, be inherited from previously altered wall rocks. Two of the four intrusions are host to Cu-Mo-rich intrusive breccias and porphyry-type mineralization which formed as much as 14 Ma after the main subvolcanic magmatic activity. The recognition of these Precambrian, subvolcanic composite intrusions is important for greenfields VMS exploration, as they define the location of thermal corridors within extensional oceanic-arc regimes which have the greatest potential for significant VMS mineralization. The VMS mineralization may occur for 2,000 m above the intrusions. In some cases, VMS mineralization has been truncated or enveloped by late trondhjemite phases of the composite intrusions. Evidence that much of the trondhjemitic magmatism postdates the principal VMS activity is a critical factor when developing heat and fluid flow models for these subseafloor magmatic-hydrothermal systems.