Combining shock barometry with numerical modeling: Insights into complex crater formation—The example of the Siljan impact structure (Sweden)

Siljan, central Sweden, is the largest known impact structure in Europe. It was formed at about 380 Ma, in the late Devonian period. The structure has been heavily eroded to a level originally located underneath the crater floor, and to date, important questions about the original size and morphology of Siljan remain unanswered. Here we present the results of a shock barometry study of quartz‐bearing surface and drill core samples combined with numerical modeling using iSALE. The investigated 13 bedrock granitoid samples show that the recorded shock pressure decreases with increasing depth from 15 to 20 GPa near the (present) surface, to 10–15 GPa at 600 m depth. A best‐fit model that is consistent with observational constraints relating to the present size of the structure, the location of the downfaulted sediments, and the observed surface and vertical shock barometry profiles is presented. The best‐fit model results in a final crater (rim‐to‐rim) diameter of ~65 km. According to our simulations, the original Siljan impact structure would have been a peak‐ring crater. Siljan was formed in a mixed target of Paleozoic sedimentary rocks overlaying crystalline basement. Our modeling suggests that, at the time of impact, the sedimentary sequence was approximately 3 km thick. Since then, there has been around 4 km of erosion of the structure.     

Irish Carboniferous conodonts record maturation levels and the influence of tectonism, igneous activity and mineralization

Organic maturation patterns in the Lower Carboniferous of Ireland have been determined from conodont colour alteration indices (CAI) for some 750 localities. Onshore Ireland conodonts record increasing maturation in the Carboniferous rocks from the oil-window rocks of the north-east, southwards to the greenschist meta-argillite regime of the Munster Basin. In detail the Caledonoid trend has a marked influence in the Midlands, whilst in the south sharp variations in CAI are interpreted as being caused by thrusting of the Variscan Orogeny. In the south-east low maturities in the Wexford Half-graben indicate that the region was shielded from orogenic stresses, probably by the Leinster Massif. Igneous centres such as the Carlingford Complex and Croghan Hill produce local sites of increased palaeotemperature. Significant CAI variations have also been noted in proximity to major base-metal orebodies. The CAI results highlight north-east Ireland and the Wexford Half-Graben as areas with hydrocarbon potential.     

Eolian controlled modification of the martian south polar layered deposits

Data from the Mars Orbiter Laser Altimeter (MOLA) and Mars Orbiter Camera (MOC) aboard the Mars Global Surveyor (MGS) mission and the Thermal Emission Imaging System (THEMIS) aboard the Mars Odyssey mission have revealed unique surface features in a particular region of the South Polar Layered Deposits (SPLD). The dominant morphology is large-scale quasi-parallel grooves that extend for hundreds of kilometers with only tens of meters of vertical relief, that we have termed here the “Wire Brush” terrain. The grooves are also transected by disjointed, yet roughly continuous, low-relief sinuous ridges that cross roughly perpendicular to the trend-direction of the large-scale grooves and show only tens of meters of relief. We interpret these ridges to be eroded remnants of folded layers. At the northern end of the large-scale grooves there are non-symmetric mounds. They are frequently preceded by a significant depression and/or trailing grooves that are parallel to the Wire Brush trend. We find that a two-stage process involving winds that intermittently remove a low-density crust exposing the underlying ice to ablation is the interpretation that best explains the multitude of features observed here. These features appear to be currently inactive indicating higher winds in previous epochs.     

Paleolimnology of McNearney lake: an acidic lake in northern Michigan

McNearney Lake is an acidic (pH=4.4) lake in the Upper Peninsula of Michigan with low acid neutralizing capacity (ANC=-38 eq L^-1) and high SO _inf4 ^sup2- and aluminium concentrations. Oligotrophy is indicated by high Secchi transparency and by low chlorophyll a, total phosphorus, and total nitrogen concentrations. The lake water is currently acidic because base cations are supplied to the lake water at a low rate and because SO _inf4 ^sup2- from atmospheric deposition was not appreciably retained by the lake sediments or watershed and was present in the water column.This interdisciplinary paleolimnological study indicates that McNearney Lake is naturally acidic and has been so since at least 4000 years B.P., as determined from inferred-pH techniques based on contemporary diatom-pH relationships. Predicted pH values ranged from 4.7 to 5.0 over the 4000-year stratigraphy. Considerable shifts in species composition and abundance were observed in diatom stratigraphy, but present-day distributions indicate that all abundant taxa most frequently occur under acidic conditions, suggesting that factors other than pH are responsible for the shifts. The diatom-inferred pH technique as applied to McNearney Lake has too large an uncertainly and is not sensitive enough to determine the subtle recent changes in lakewater pH expected from changes in atmospheric deposition because: (1) McNearney Lake has the lowest pH in the contemporary diatom data set in the region and confidence intervals for pH predictions increase at the extremes of regressions; (2) other factors in addition to pH may be responsible for the diatom species distribution in the lake and in the entire northern Great Lakes region; (3) McNearney Lake has a well-buffered pH as a consequence of its low pH and high aluminium concentrations and is not expected to exhibit a large pH change as a result of changes in atmospheric deposition; and (4) atmospheric deposition in the region is modest and would not cause a pH shift large enough to be discernable in McNearney Lake.Elevated atmospheric deposition is indicated in recent sediments by Pb, V, and polycyclic aromatic hydrocarbon accumulation rates and to a lesser extent by those of Cu and Zn; however, these accumulation rates are substantially lower than those observed for acidified lakes in the northeastern United States. Although atmospheric loadings of materials associated with fossil fuel combustion have recently increased to McNearney Lake and apparently are continuing, the present study of the diatom subfossil record does not indicate a distinct, recent acidification (pH decrease).Order of the first two authors is alphabetical     

An iron isotope signature related to electron transfer between aqueous ferrous iron and goethite

We measured the Fe isotope fractionation during the reactions of Fe(II) with goethite in the presence and absence of a strong Fe(III) chelator (desferrioxamine mesylate, DFAM). All experiments were completed in an O₂-free glove box. The concentrations of aqueous Fe(II) ([Fe(II)_aq]) decreased below the initial total dissolved Fe concentrations ([Fe(II)_total], 2.15 mM) due to fast adsorption within 0.2 day. The concentration of adsorbed Fe(II) ([Fe(II)_ads]) was determined as the difference between [Fe(II)_aq] and the concentration of extracted Fe(II) in 0.5 M HCl ([Fe(II)_extr]) (i.e., [Fe(II)_ads] = [Fe(II)_extr] − [Fe(II)_aq]). [Fe(II)_ads] also decreased with time in experiments with and without DFAM, documenting that fast adsorption was accompanied by a second, slower reaction. Interestingly, [Fe(II)_extr] was always smaller than [Fe(II)_total], indicating that some Fe(II) was sequestered into a pool that is not HCl-extractable. The difference was attributed to Fe(II) incorporated into goethite structure (i.e., [Fe(II)_inc] = [Fe(II)_total] −[Fe(II)_extr]). More Fe(II) was incorporated in the presence of DFAM than in its absence at all time steps. Regardless of the presence of DFAM, both aqueous and extracted Fe(II) (δ^56/54Fe(II)_aq and δ^56/54Fe(II)_extr) became isotopically lighter than or similar to goethite (− 0.27‰) at day 7, implying that the isotope exchange occurred between bulk goethite and aqueous Fe. Consistently, the mass balance indicated that the incorporated Fe is isotopically heavier than extracted Fe. These observations suggested that (i) co-adsorption of Fe(II) with DFAM resulted in more pervasive electron transfer, (ii) the electron transfer from heavy Fe(II) in the adsorbed Fe(II) to light Fe(III) in goethite results in the fixation of heavy adsorbed Fe(III) on the surface and accumulation of Fe(II) within the goethite, and (iii) desorption of the reduced, light Fe from goethite does not necessarily occur at the same surface sites where adsorption occurred.     

The Othris Ophiolite, Greece: A snapshot of subduction initiation at a mid-ocean ridge

The mantle section of the Tethyan-type Othris Ophiolite, Greece, records tectono-magmatic processes characteristic of both mid-ocean ridges and supra-subduction zones. The Othris Ophiolite is a remnant of the Jurassic Neotethys Ocean, which existed between Eurasia and Gondwanaland. Othris peridotites range from fertile plagioclase lherzolites to depleted harzburgites. Abundances of Al₂O₃ and CaO show well-defined inverse linear correlations with MgO, suggesting that the Othris peridotites formed as residua from variable degrees of partial melting.

Peridotites from the Fournos Kaïtsa and western Katáchloron sub-massifs are similar to abyssal peridotites and can be explained by a multistage model with some melting in the garnet stability field followed by moderate degrees of anhydrous near-fractional melting in the spinel stability field. In contrast, the peridotites from the Metalleio, Eretria, and eastern Katáchloron sub-massifs, and the Vourinos ophiolite are highly depleted and have extremely low concentrations of Al₂O₃ and heavy rare earth elements. These peridotites have enriched light REE contents compared to the middle REE. These residua are best modelled by hydrous melting due to a flux of slab-derived fluid to the mantle wedge during melting.

The occurrence of both styles of melting regimes within close spatial and temporal association in the same ophiolite is explained by intra-oceanic thrusting and forced subduction initiation at (or near) a mid-ocean ridge. Thus, the Othris Ophiolite, and probably Tethyan-type ophiolites in general, represent a transient phase of plate tectonic reorganisation rather than quasi-steady state plate tectonics.     

Composition of widespread volcanic glass in deep-sea sediments of the Southern Pacific Ocean: an Antarctic source inferred

Widespread Plio-Pleistocene (2.43-0.06 Ma) tephra zones recognised in deep-sea cores from high latitudes (>60°) in the Southern Pacific Ocean were thought to have originated from calc-alkaline rhyolitic eruptions in New Zealand, some 5000 km distant. Electron microprobe analyses of the glasses reveal a wide diversity of alkalic felsic compositions, as well as minor components of basic and intermediate glasses, incompatible with a New Zealand Neogene source but similar to contemporaneous eruptives from the Antarctic region. Most tephra zones are trachytic; seven zones are peralkaline rhyolite. The rhyolitic zones represent a deep-sea record of widespread silicic eruptions from continental Antarctica, possibly Marie Byrd Land. The extent of these rhyolitic zones suggest a greater frequency of large explosive eruptions in Antarctica than previously documented. The coarse grain size of some of the shards (up to 3 mm), their great distance from the closest sources (>1600 km for some cores), and the presence of nonvolcanic ice-rafted debris indicate some of the glasses, especially the more basic compositions, may have been ice-rafted, contrary to previous suggestions of a fallout origin.     

Fluid venting and seepage at accretionary ridges: the Four Way Closure Ridge offshore SW Taiwan

Within the accretionary prism offshore SW Taiwan, widespread gas hydrate accumulations are postulated to occur based on the presence of a bottom simulating reflection. Methane seepage, however, is also widespread at accretionary ridges offshore SW Taiwan and may indicate a significant loss of methane bypassing the gas hydrate system. Four Way Closure Ridge, located in 1,500 m water depth, is an anticlinal ridge that would constitute an ideal trap for methane and consequently represents a site with good potential for gas hydrate accumulations. The analysis of high-resolution bathymetry, deep-towed sidescan sonar imagery, high-resolution seismic profiling and towed video observations of the seafloor shows that Four Way Closure Ridge is and has been a site of intensive methane seepage. Continuous seepage is mainly evidenced by large accumulations of authigenic carbonate precipitates, which appear to be controlled by the creation of fluid pathways through faulting. Consequently, Four Way Closure Ridge is not a closed system in terms of fluid migration and seepage. A conceptual model of the evolution of gas hydrates and seepage at accretionary ridges suggests that seepage is common and may be a standard feature during the geological development of ridges in accretionary prisms. The observation of seafloor seepage alone is therefore not a reliable indicator of exploitable gas hydrate accumulations at depth.