Methane-derived authigenic carbonates from active hydrocarbon seeps of the St. Lawrence Estuary,Canada

Nearly 2000 pockmarks with diameters ranging from a few tens of meters up to 700 m are present on the seafloor of the St. Lawrence Estuary in eastern Canada. Coring of some pockmarks resulted in the recovery of various-sized and shaped carbonate concretions in a predominantly silty mud matrix. Petrographic and geochemical data on four authigenic carbonate concretions are reported as well as data from shell material in the unconsolidated sediment. Video observations and echo-sounder images indicate that the sampled pockmarks are actively gas venting. The video images show significant look-alike microbial mats in areas where gas is venting. The carbonate concretions are primarily made up of carbonate cements with varying percentage of shell fragments, micrite particles and fine-grained clastics. Orthorhombic crystal morphology and diagenetic fabrics including isopachous layers and botryoids characterize the aragonite cement. Oxygen isotopes ratios for the cement crusts do not record any thermal anomaly at the site of precipitation with δ¹⁸O_VPDB ratios (+3‰) in equilibrium with cold (5 °C) deep marine waters, whereas significant negative δ¹³C_VPDB ratios (−9.9 to −33.5‰) for cement and shell material within concretions indicate that the carbonates largely derive from the microbial oxidation of methane. The δ¹³C_VPDB ratios of aragonite shells (−2.7 to −5.6‰) taken from unconsolidated sediments at some distance from the concretions/vents show variable dilution of HCO₃⁻ with negative δ¹³C_VPDB ratios derived from microbial oxidation of methane with isotopically normal (0‰) marine bicarbonate. These results are in agreement with other lines of evidence suggesting that pockmarks formed through the recent and still active release of gas from a reservoir within the Paleozoic sedimentary succession.     

Ilmenite composition in the Tellnes Fe–Ti deposit,SW Norway: fractional crystallization,postcumulus evolution and ilmenite–zircon relation

Major and trace element XRF and in situ LA-ICP-MS analyses of ilmenite in the Tellnes ilmenite deposit, Rogaland Anorthosite Province, SW Norway, constrains a two stage fractional crystallization model of a ferrodioritic Fe-Ti-P rich melt. Stage 1 is characterized by ilmenite-plagioclase cumulates, partly stored in the lower part of the ore body (Lower Central Zone, LCZ), and stage 2 by ilmenite-plagioclase-orthopyroxene-olivine cumulates (Upper Central Zone, UCZ). The concentration of V and Cr in ilmenite, corrected for the trapped liquid effect, (1) defines the cotectic proportion of ilmenite to be 17.5 wt% during stage 1, and (2) implies an increase of D _V^Ilm during stage 2, most likely related to a shift in fO₂. The proportion of 17.5 wt% is lower than the modal proportion of ilmenite (ca. 50 wt%) in the ore body, implying accumulation of ilmenite and flotation of plagioclase. The fraction of residual liquid left after crystallization of Tellnes cumulates is estimated at 0.6 and the flotation of plagioclase at 26 wt% of the initial melt mass. The increasing content of intercumulus magnetite with stratigraphic height, from 0 to ca. 3 wt%, results from differentiation of the trapped liquid towards magnetite saturation. The MgO content of ilmenite (1.4–4.4 wt%) is much lower than the expected cumulus composition. It shows extensive postcumulus re-equilibration with trapped liquid and ferromagnesian silicates, correlated with distance to the host anorthosite. The Zr content of ilmenite, provided by in situ analyses, is low (<114 ppm) and uncorrelated with stratigraphy or Cr content. The data demonstrate that zircon coronas observed around ilmenite formed by subsolidus exsolution of ZrO₂ from ilmenite. The U-Pb zircon age of 920 ± 3 Ma probably records this exsolution process. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Analyzing seismic imagery in the time–amplitude and time–frequency domains to determine fluid nature and migration pathways: A case study from the Queen Charlotte Basin,offshore British Columbia

Combining time–amplitude and time–frequency information from seismic reflection data sets of different resolutions allows the analysis of anomalous reflections from very-shallow to great subsurface depths. Thus, it can enhance the imaging of subsurface features which have a frequency-dependent reflectivity such as gas. Analysing seismic data of different resolution in the time–amplitude and time–frequency domains is a powerful method to determine hydrocarbon migration pathways from deep reservoirs to the seafloor. This interpretation method has been applied to the formerly-glaciated offshore Queen Charlotte Basin hosting several seafloor pockmarks and mounds associated with the leakage of underlying hydrocarbon reservoirs. Low-frequency shadows observed in the time–frequency domain provide evidence of different resolutions that several anomalous reflection amplitudes may be attributed to the occurrence of gas. The seismic imagery shows that gas uses a fault to migrate from deep reservoirs included in Upper Mesozoic strata towards secondary reservoirs located along the fault plane into Neogene layers. Once gas reaches a porous cut-and-fill succession, migration changes from structurally- to stratigraphically-controlled before gas leaks through unconsolidated Quaternary sediments forming the shallow subsurface to eventually seep at the seafloor where pockmarks and carbonate mounds are formed.     

Linking a linear pockmark train with a buried Palaeozoic structure: a case study from the St. Lawrence Estuary

The 15-km-long Matane pockmark train belongs to a series of NNE-striking alignments of pockmarks mapped on the seafloor of the St. Lawrence Estuary. It includes 109 pockmarks that show a complete transition from well-defined, relatively deep (up to 8.6 m), crater-like depressions to subtle, partly buried morphological features, suggesting that pockmarks have formed at different periods along the whole alignment and that the location of fluid release has changed through time. On seismic profiles, pockmarks are characterized by vertical seismic chimneys that root in the (fractured?) hinge zone of an open anticline within the autochthonous Palaeozoic rocks of the St. Lawrence Platform. In absence of a geochemical characterization of expelled gas, the relationship between the Matane pockmark train and the anticline in a domain characterized by mature source rocks is the strongest evidence for the genetic link between pockmarks and the release of gas from an active hydrocarbon system or a reservoir located in the Palaeozoic succession.

Rare-earth data on monzonoritic rocks related to anorthosites and their bearing on the nature of the parental magma of the anorthositic series

Major and trace elements have been determined in monzonoritic rocks (hypersthene-monzodiorite or jotunite) from two intrusions belonging to the South Rogaland anorthositic complex (Norway). The rare-earth abundance pattern reveals no Eu anomaly, or only a very small one. This fact together with field observations suggest that these rocks represent the parental magma of the anorthositic suite. High Ti and P abundances, low Si content, high Fe/Mg and K₂O/SiO₂ ratios are characteristics of the major element geochemistry. Absolute amounts of some trace elements abundances vary distinctly between the two intrusions. K/Rb ratios as high as 1700 are observed. Partial fusion of upper mantle kaersutite is proposed as a possible mechanism of magma generation. Partition coefficients between plagioclase phenocrysts and liquid are determined.     

Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway) Part II. REE and the trapped liquid fraction

Rare earth elements in bulk cumulates and in separated minerals (plagioclase, apatite, Ca-poor and Ca-rich pyroxenes, ilmenite and magnetite) from the Bjerkreim–Sokndal layered intrusion (Rogaland Anorthosite Province, SW Norway) are investigated to better define the proportion of trapped liquid and its influence on bulk cumulate composition. In leuconoritic rocks (made up of plagioclase, Ca-poor pyroxene, ilmenite, ±magnetite, ±olivine), where apatite is an intercumulus phase, even a small fraction of trapped liquid significantly affects the REE pattern of the bulk cumulate, together with cumulus minerals proportion and composition. Contrastingly, in gabbronoritic cumulates characterized by the presence of cumulus Ca-rich pyroxene and apatite, cumulus apatite buffers the REE content. La/Sm and Eu/Eu* vs. P₂O₅ variations in leuconorites display mixing trends between a pure adcumulate and the composition of the trapped liquid, assumed to be similar to the parental magma. Assessment of the trapped liquid fraction in leuconorites ranges from 2 to 25% and is systematically higher in the north-eastern part of the intrusion. The likely reason for this wide range of TLF is different cooling rates in different parts of the intrusion depending on the distance to the gneissic margins. The REE patterns of liquids in equilibrium with primitive cumulates are calculated with mass balance equations. Major elements modelling (Duchesne, J.C., Charlier, B., 2005. Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway): Part I. Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent. Lithos. 83, 299–254) permits calculation of the REE content of melt in equilibrium with gabbronorites. Partition coefficients for REE between cumulus minerals and a jotunitic liquid are then calculated. Calculated liquids from the most primitive cumulates are similar to a primitive jotunite representing the parental magma of the intrusion, taking into account the trapped liquid fraction calculated from the P₂O₅ content. Consistent results demonstrate the reliability of liquid compositions calculated from bulk cumulates and confirm the hypothesis that the trapped liquid has crystallized as a closed-system without subsequent mobility of REE in a migrating interstitial liquid.     

Marginal mafic intrusions as indicators of downslope draining of dense residual melts in anorthositic diapirs?

Geochemical and isotopic investigation of three small mafic intrusions (Løyning: 1250 × 150 m, Hogstad: 2000 × 200 m, Koldal: 1250 × 500 m) in the marginal zones of the Egersund-Ogna (Løyning, Koldal) and Åna-Sira massif-type anorthosites (Hogstad) (Rogaland Anorthositic Province, south Norway: 930 Ma) provides new insights into the late evolution of anorthositic diapirs. These layered mafic intrusions are essentially of norite, gabbronorite as well as leuconorite and display conspicuous evidence of subsolidus recrystallization. In Løyning and Hogstad, the modal layering is parallel to the subvertical foliation in the enclosing anorthosite. The northern part of the Koldal intrusion cuts across the foliation of the anorthosite, whereas in its southern part the subvertical layering is parallel to the anorthosite's foliation. The regularity of the layered structures suggests that the layering was initially acquired horizontally and later tilted during the final movements of the diapirs.

The least differentiated compositions of plagioclase and orthopyroxene in the three intrusions (An₅₉–En₆₈ in Løyning, An₄₉–En₆₄ in Hogstad and An₄₄–En₆₁ in Koldal) and the REE contents in apatite (Hogstad) indicate that their parent magmas were progressively more differentiated in the sequence Løyning–Hogstad–Koldal. Isotopic data (Løyning: ⁸⁷Sr/⁸⁶Sr: 0.70376–0.70457, ε_Ndt: + 6.8 to + 2.7; Hogstad: ⁸⁷Sr/⁸⁶Sr: 0.70537–0.70588, ε_Ndt: + 2.1 to − 0.5; Koldal: ⁸⁷Sr/⁸⁶Sr: 0.70659–0.70911, ε_Ndt: + 3.5 to − 1.6) also indicate that in this sequence, parent magmas were characterized by a progressively more enriched Sr and Nd isotopic signature. In Løyning, the parent magma was slightly more magnesian and anorthitic than a primitive jotunite; in Hogstad, it is a primitive jotunite; and, in Koldal, an evolved jotunite. Given that plagioclase and orthopyroxene of the three intrusions display more differentiated compositions than the orthopyroxene and plagioclase megacryts of the enclosing anorthosites, it is suggested that the parent magmas of the small intrusions are residual melts after anorthosite formation which were entrained in the anorthositic diapir during its rise from lower crustal chambers.

Calculated densities of primitive jotunites (2.73–2.74 at FMQ, 0.15% H₂O, 200 ppm CO₂, 435 ppm F, 1150 °C, 3 kb) and evolved jotunites (2.75–2.76 at FMQ, 0.30% H₂O, 400 ppm CO₂, 870 ppm F, 1135 °C, 3 kb) demonstrate that they are much denser than the plagioclase of the surrounding anorthositic crystal mush (2.61–2.65). Efficient migration and draining of dense residual melts through the anorthositic crystal mush could have taken place along sloping floors (zones of lesser permeability in the mush), which occur along the margins of the rising anorthositic diapirs. This process takes into account the restricted occurrence of the mafic intrusions in the margins of the massif anorthosites. In a later stage, when the anorthosite was nearly consolidated, the residual melts were more differentiated (evolved jotunites) and could have been extracted into extensional fractures in the cooling and contracting anorthositic body in a similar way as aplitic dikes are emplaced in granitic plutons. As in the Rogaland Anorthositic Province, these dikes are much more abundant than the small mafic intrusions, collection and transport along dikes was probably more efficient than draining through the crystal mush.     

Response to the Discussion by B. Robins and F. Chiodoni of “Geochemistry of cumulates from the Bjerkreim–Sokndal Intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent”

Merging our data with those of Robins and Chiodoni [Robins, B., Chiodoni, F., 2007. Poles apart: A discussion of the « Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent ». Lithos doi:10.1016/j.lithos.2007.03.007], we examine the major-element compositions of 135 samples of so-called phi-C cumulates of the Bjerkreim–Sokndal layered intrusion. We show the limits of the TiO₂/MgO ratio vs. Al₂O₃ diagram in order to ascertain the proportions of cumulus minerals (ilmenite and orthopyroxene) in the ilmenite leuconorite mafic pole. We also discard anomalous samples as we did in the previous paper. The rest of the samples (124 phi-C, i.e. 92% of the whole population) are then used to confirm the existence of plagioclase and mafic poles. It is shown that the mafic pole is indeed a mixture of ilmenite and orthopyroxene, not induced by “spurious correlation”.     

A rapid method for converting medical Computed Tomography scanner topogram attenuation scale to Hounsfield Unit scale and to obtain relative density values

Medical Computed Tomography scanners permit to rapidly obtain qualitative and quantitative information on objects in a non-destructive manner in both longitudinal and transversal directions. CT-scan scales used to express attenuation on the images are different for longitudinal (topograms) and transversal (tomograms) views, restraining the complementary use of the information extracted from both views. Moreover, topograms are of full use in core analysis as they reveal fine-scale information on stratigraphical, sedimentological and physical properties of the material. This paper presents a method to convert CT-scan topogram intensity scale to Hounsfield Unit (HU; scale used on tomograms) and to later extract a relative density from it. The method is based on relationships between topogram and tomogram values, absolute density and effective atomic numbers obtained on a series of minerals. Results show excellent correlations between converted topogram values and HU values obtained on the tomograms, as well as between relative densities derived from the converted topogram values, and the absolute density of the minerals.