| 1. |
|
|
| 2. |
- Breitfeld, H. T., et al.
(författare)
-
The onshore West Baram Delta deposits: Provenance and drainage in the Middle Miocene to Pliocene in NW Borneo and comparison to the Champion Delta
- 2023
-
Ingår i: Marine and Petroleum Geology. - 0264-8172. ; 158
-
Tidskriftsartikel (refereegranskat)abstract
- The Baram Delta province in NW Borneo forms a major hydrocarbon reservoir offshore northern Sarawak and Brunei. The delta sequence is thereby subdivided into the West Baram delta to the south and the Champion delta to the north. Onshore are the remains of the Neogene delta deposits exposed and provide the possibility to study the equivalent offshore successions in outcrop. This study focuses on the Neogene West Baram delta successions which were studied for sedimentological facies and provenance characteristics. The successions consist of the Lambir, Miri, Tukau, and the enigmatic southern Lambir/Belait-Sarawak formations. Deposition took place in various mixed-energy delta environments between the Langhian and early Pliocene. The sediments are all quartzrich and heavy minerals are dominated by ultra-stable zircon, rutile and tourmaline. Dominant detrital zircon age clusters are in the Early Cretaceous and Permian-Triassic. Based on light mineral petrography, heavy mineral assemblages, and detrital zircon U-Pb geochronology, all formations are interpreted as derived from multirecycled sources, likely the underlying Paleogene Rajang Group turbidites and the Oligocene to Lower Miocene Nyalau-Tatau delta deposits. Additionally, literature data of the Champion Delta and one sample from Labuan analysed for provenance in this study are used to demonstrate that the Champion Delta can be distinguished from the West Baram Delta by having higher chrome spinel and garnet contents and slightly different detrital zircon age populations. The Champion Delta deposits are interpreted as sourced by recycling of the Crocker Formation and older turbidites (e.g., Sapulut Formation) with potentially input from ultra-mafic basement rocks of Sabah.
|
|
| 3. |
- Fox, Sydney, et al.
(författare)
-
Physical characteristics of microplastic particles and potential for global atmospheric transport: A meta-analysis
- 2024
-
Ingår i: Environmental Pollution. - 0269-7491 .- 1873-6424. ; 342
-
Forskningsöversikt (refereegranskat)abstract
- Recent interest in microplastic pollution of natural environments has brought forth samples which confirm the pollutant's omnipresence in a variety of ecosystems. This includes locations furthest removed from human activity. Atmospheric transport and deposition are suspected as the primary transport pathway to these remote locations. The factors most influential on participation in atmospheric transport are yet to be determined. This meta-analysis aims to identify patterns that exist between physical characteristics of microplastic particles and their potential for atmospheric transport. Our review addresses the following questions: Which characteristics of microplastic particles promote atmospheric transport and deposition into remote regions, and how significant are these factors in determining distance transported from their sources? This article analyzes commonly reported physical attributes– shape, polymer composition and color– from studies in urban and remote areas. The analysis of 68 studies, composed of data from 2078 samples, shows higher occurrence of microplastic particles in remote samples with fiber shapes, polyester compositions, and red, blue, and transparent colors. This meta-analysis is the first to identify patterns between physical properties of microplastic particles and extent of their participation in atmospheric transport to global remote locations.
|
|
| 4. |
- Halama, R., et al.
(författare)
-
Boron isotope record of peak metamorphic ultrahigh-pressure and retrograde fluid-rock interaction in white mica (Lago di Cignana, Western Alps)
- 2020
-
Ingår i: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 175:3
-
Tidskriftsartikel (refereegranskat)abstract
- This study presents boron (B) concentration and isotope data for white mica from (ultra)high-pressure (UHP), subduction-related metamorphic rocks from Lago di Cignana (Western Alps, Italy). These rocks are of specific geological interest, because they comprise the most deeply subducted rocks of oceanic origin worldwide. Boron geochemistry can track fluid-rock interaction during their metamorphic evolution and provide important insights into mass transfer processes in subduction zones. The highest B contents (up to 345 mu g/g B) occur in peak metamorphic phengite from a garnet-phengite quartzite. The B isotopic composition is variable (delta B-11 = - 10.3 to - 3.6%) and correlates positively with B concentrations. Based on similar textures and major element mica composition, neither textural differences, prograde growth zoning, diffusion nor a retrograde overprint can explain this correlation. Modelling shows that B devolatilization during metamorphism can explain the general trend, but fails to account for the wide compositional and isotopic variability in a single, well-equilibrated sample. We, therefore, argue that this trend represents fluid-rock interaction during peak metamorphic conditions. This interpretation is supported by fluid-rock interaction modelling of boron leaching and boron addition that can successfully reproduce the observed spread in delta B-11 and [B]. Taking into account the local availability of serpentinites as potential source rocks of the fluids, the temperatures reached during peak metamorphism that allow for serpentine dehydration, and the high positive delta B-11 values (delta B-11 = 20 +/- 5) modelled for the fluids, an influx of serpentinite-derived fluid appears likely. Paragonite in lawsonite pseudomorphs in an eclogite and phengite from a retrogressed metabasite have B contents between 12 and 68 mu g/g and delta B-11 values that cluster around 0% (delta B-11 = - 5.0 to + 3.5). White mica in both samples is related to distinct stages of retrograde metamorphism during exhumation of the rocks. The variable B geochemistry can be successfully modelled as fluid-rock interaction with low-to-moderate (< 3) fluid/rock ratios, where mica equilibrates with a fluid into which B preferentially partitions, causing leaching of B from the rock. The metamorphic rocks from Lago di Cignana show variable retention of B in white mica during subduction-related metamorphism and exhumation. The variability in the B geochemical signature in white mica is significant and enhances our understanding of metamorphic processes and their role in element transfer in subduction zones.
|
|
| 5. |
|
|
| 6. |
- Halama, R., et al.
(författare)
-
Rb-Sr and in situ Ar-40/Ar-39 dating of exhumation-related shearing and fluid-induced recrystallization in the Sesia zone (Western Alps, Italy)
- 2018
-
Ingår i: Geosphere. - : Geological Society of America. - 1553-040X. ; 14:4, s. 1425-1450
-
Tidskriftsartikel (refereegranskat)abstract
- The Sesia zone in the Italian Western Alps is a piece of continental crust that has been subducted to eclogite-facies conditions and records a complex metamorphic history. The exact timing of events and the significance of geochronological information are debated due to the interplay of tectonic, metamorphic, and metasomatic processes. Here we present new geochronological data using Rb-Sr internal mineral isochrons and in situ Ar-40/Ar-39 laser ablation data to provide constraints on the relative importance of fluid-mediated mineral replacement reactions and diffusion for the interpretation of radiogenic isotope signatures, and on the use of these isotopic systems for dating metamorphic and variably deformed rocks. Our study focuses on the shear zone at the contact between two major lithological units of the Sesia zone, the eclogitic micaschists and the gneiss minuti. Metasedimentary rocks of the eclogitic micaschists unit contain phengite with step-like zoning in major element chemistry as evidence for petrologic disequilibrium. Distinct Ar-40/Ar-39 spot ages of relict phengite cores and over-printed rims demonstrate the preservation of individual age domains in the crystals. The eclogitic micaschists also show systematic Sr isotope disequilibria among different phengite populations, so that minimum ages of relict assemblage crystallization can be differentiated from the timing of late increments of deformation. The preservation of these disequilibrium features shows the lack of diffusive re-equilibration and underpins that fluid-assisted dissolution and recrystallization reactions are the main factors controlling the isotope record in these subduction-related metamorphic rocks. Blueschist-facies mylonites record deformation along the major shear zone that separates the eclogitic micaschists from the gneiss minuti. Two Rb-Sr isochrones that comprise several white mica fractions and glaucophane constrain the timing of this deformation and accompanying near-complete blueschist-facies re-equilibration of the Rb-Sr system to 60.1 +/- 0.9 Ma and 60.9 +/- 2.1 Ma, respectively. Overlapping ages in eclogitic micaschists of 60.1 +/- 1.1 (Rb-Sr isochron of sheared matrix assemblage), 58.6 +/- 0.8, and 60.9 +/- 0.4 Ma (white mica Ar-40/Ar-39 inverse isochron ages) support the significance of this age and show that fluid-rock interaction and partial re-equilibration occurred as much as several kilometers away from the shear zone. An earlier equilibration during high-pressure conditions in the eclogitic mica schists is recorded in minimum Rb-Sr ages for relict assemblages (77.2 +/- 0.8 and 72.4 +/- 1.1 Ma) and an Ar-40/Ar-39 inverse isochron age of 75.4 +/- 0.8 Ma for white mica cores, again demonstrating that the two isotope systems provide mutually supporting geochronological information. Local reactivation and recrystallization along the shear zone lasted >15 m.y., as late increments of deformation are recorded in a greenschist-facies mylonite by a Rb-Sr isochron age of 46.5 +/- 0.7 Ma.
|
|
| 7. |
|
|
| 8. |
|
|
| 9. |
- Karlsson, Andreas, 1986-, et al.
(författare)
-
Adding complexity to the garnet supergroup: monteneveite, Ca3Sb5+2(Fe3+2Fe2+)O12, a new mineral from the Monteneve mine, Bolzano Province, Italy
- 2020
-
Ingår i: European Journal of Mineralogy. - : Copernicus GmbH. - 0935-1221 .- 1617-4011. ; 32:1, s. 77-87
-
Tidskriftsartikel (refereegranskat)abstract
- Monteneveite, ideally Ca3Sb5+2(Fe3+2Fe2+)O12, is a new member of the garnet supergroup (IMA 2018-060). The mineral was discovered in a small specimen belonging to the Swedish Museum of Natural History coming from the now abandoned Monteneve Pb-Zn mine in Passiria Valley, Bolzano Province, Alto Adige (South Tyrol), Italy. The specimen consists of mainly magnetite, sphalerite, tetrahedrite-(Fe) and oxycalcioroméite. Monteneveite occurs as black, subhedral crystals with adamantine lustre. They are equidimensional and up to 400 μm in size, with a subconchoidal fracture. Monteneveite is opaque, grey in reflected light, and isotropic under crossed polars. Measured reflectance values (%) at the four COM wavelengths are 12.6 (470 nm), 12.0 (546 nm), 11.6 (589 nm) and 11.4 (650 nm). The Vickers hardness (VHN100/ is 1141 kgmm-2, corresponding to H D 6:5-7, and the calculated density is 4.72(1) g cm-3. A mean of 10 electron microprobe analyses gave (wt %) CaO 23.67, FeO 3.75, Fe2O3 29.54, Sb2O5 39.81, SnO2 2.22, ZnO 2.29, MgO 0.15, MnO 0.03 and CoO 0.03. The crystal chemical formula calculated on the basis of a total of eight cations and 12 anions, and taking into account the available structural and spectroscopic data, is (Ca2:97Mg0:03)6D3:00 (Sb5+1.73Sn4+0.10Fe3+0.17)6D2.00(Fe3+2.43Fe2+0.37Zn0:20)6D3:00O12. The most significant chemical variations encountered in the sample are related to a substitution of the type Y Sn4CCZFe3CY Sb5CCZFe2C. Mössbauer data obtained at RT and 77K indicate the presence of tetrahedrally coordinated Fe2C. Raman spectroscopy demonstrates that there is no measurable hydrogarnet component in monteneveite. The six strongest Bragg peaks in the powder X-ray diffraction pattern are [d (Å), I (%), (hkl)]: 4.45, 100, (220); 3.147, 60, (400); 2.814, 40, (420); 2.571, 80, (422); 1.993, 40, (620); 1.683, 60, (642). Monteneveite is cubic, space group Ia-3d, with a D 12:6093(2) Å, V D 2004:8(1)Å3, and Z D 8. The crystal structure was refined up to R1 D 0:0197 for 305 reflections with Fo 4.Fo/ and 19 parameters. Monteneveite is related to the other Ca-, Sb- and Fe-bearing, nominally Si-free members of the bitikleite group, but it differs in that it is the only known garnet species with mixed trivalent and divalent cations (2 V 1) at the tetrahedral Z site. Textural and mineralogical evidence suggests that monteneveite formed during peak metamorphism (at ca. 600 C) during partial breakdown of tetrahedrite-(Fe) by reactions with carbonate, under relatively oxidizing conditions. The mineral is named after the type locality, the Monteneve (Schneeberg) mine. © Author(s) 2020.
|
|
| 10. |
- Konrad-Schmolke, Matthias, 1970, et al.
(författare)
-
Combined thermodynamic and rare earth element modelling of garnet growth during subduction: Examples from ultrahigh-pressure eclogite of the Western Gneiss Region, Norway
- 2008
-
Ingår i: Earth and Planetary Science Letters. - 0012-821X. ; 272:1-2, s. 488-498
-
Tidskriftsartikel (refereegranskat)abstract
- Major and trace element zonation patterns were determined in ultrahigh-pressure eclogite garnets from the Western Gneiss Region (Norway). All investigated garnets show Multiple growth zones and preserve complex growth zonation patterns with respect to both major and rare earth elements (REE). Due to chemical differences of the host rocks two types of major element compositional zonation patterns occur: (1) abrupt, step-like compositional changes corresponding with the growth zones and (2) compositionally homogeneous interiors, independent of growth zones, followed by abrupt chemical changes towards the rims. Despite differences in major element zonation, the REE patterns are almost identical in all garnets and can be divided into four distinct zones with characteristic patterns. In order to interpret the major and trace element distribution and zoning patterns in terms of the subduction history of the rocks, we combined thermodynamic forward models for appropriate bulk rock compositions to yield molar proportions and major element compositions of stable phases along the inferred pressure-temperature path with a mass balance distribution of REEs among the calculated stable phases during high pressure metamorphism. Our thermodynamic forward models reproduce the complex major element zonation patterns and growth zones in the natural garnets, with garnet growth predicted during four different reaction stages: (1) chlorite breakdown, (2) epidote breakdown, (3) amphibole breakdown and (4) reduction in molar clinopyroxene at ultrahigh-pressure conditions. Mass-balance of the rare earth element distribution among the modelled stable phases yielded characteristic zonation patterns in garnet that closely resemble those in the natural samples. Garnet growth and trace element incorporation Occurred in near thermodynamic equilibrium with matrix phases during subduction. The rare earth element patterns in garnet exhibit distinct enrichment zones that fingerprint the minerals involved in the garnet-forming reactions as well as local peaks that can be explained by fractionation effects and changes in the mineral assemblage. (C) 2008 Elsevier B.V. All rights reserved.
|
|
