PRESERVATION OF NEUROPTERIS OVATA IN ROOF SHALE AND IN FLUVIAL CREVASSE-SPLAY FACIES (LATE PENNSYLVANIAN, SYDNEY COALFIELD, CANADA). PART I: AN INFRARED-BASED CHEMOMETRIC MODEL

Palaios ◽  
2020 ◽  
Vol 35 (2) ◽  
pp. 94-109
Author(s):  
JOSÉ A. D'ANGELO ◽  
ERWIN L. ZODROW

ABSTRACT Analytical questions relating to the influence of sedimentation on the preservation states of Carboniferous plant fossils are seldom addressed in the literature. Here we address specifically the influence facies differences have on preservation states and suggest how they can be analyzed. The case study involves the seed fern Neuropteris ovata (Hoffmann) that occurs as opaque pinnules in the roof shale and as transparent pinnules in an associated crevasse-splay of the basal Cantabrian in age, Point Aconi Coal Seam, Sydney Coalfield, Canada. The color differences imply different molecular pathways for organic matter transformation over geological time, which resulted in production of compression fossils in the roof shale and fossilized-cuticle in the crevasse-splay, respectively. Fourier transform infrared spectroscopy methods are used to quantify functional groups, and the derived data are chemometrically evaluated. Results indicate that the compressions are, as anticipated, characterized in the crevasse-splay facies by a predominantly aromatic composition. The fossilized-cuticles, however, are mainly characterized by oxygen-containing aliphatics, confirming the influence of facies changes on preservation states of the species studied. Implications for preservation, taxonomy, and paleoecology are emphasized.

2012 ◽  
Vol 19 (1) ◽  
pp. 132-144 ◽  
Author(s):  
Emilie Chalmin ◽  
Yves Perrette ◽  
Bernard Fanget ◽  
Jean Susini

AbstractOrganic matter (OM) entrapped in calcite is regularly used for environmental studies; however, insertion mechanisms and types of interaction remain poorly understood. The present study used a new methodology to investigate interactions between OM and the calcite matrix during crystallization processes with humic acid (HA) entrapment. A multimethod approach confirmed that HA is both adsorbed onto the calcite surface and incorporated into the calcite lattice during crystallization. Our results also confirm the log-linear correlation between fluorescence intensity and calcite matrix HA concentration. Fourier transform infrared spectroscopy showed that HA in colloidal conformation is adsorbed onto the calcite surface as a result of the structure of the OH stretching band. We also developed a new method based on synchrotron analysis that uses sulfur as a tracer element for entrapped HA and that localizes the OM electrostatically adsorbed onto the calcite surface. Changes in the sulfur environment, determined using X-ray absorption near-edge structure spectroscopy, indicated more complex insertion mechanisms than simple adsorption of HA during calcite crystallization. Desorption experiments revealed the stability of the OM atomic structure and its layered nature. These results allowed us to draw up a general model of OM insertion in calcite.


2013 ◽  
Vol 1 (1) ◽  
pp. 17
Author(s):  
Carlos P. Odriozola ◽  
José A. Linares-Catela ◽  
Victor M. Hurtado-Pérez

In this study we discuss the exploitation and exchange of variscite at Pico Centeno mining district during the Copper Age. X-ray fluorescence and diffraction (XRF and XRD, respectively) and Fourier transform infrared spectroscopy (FTIR) analyses of the mineral recovered at Pico Centeno mining district provides a baseline mineral signature, which was then compared to other Iberian sources and beads from SW Iberian megalithic tombs. We found that the concentrations of trace elements don not allow establishing provenance of the beads, as traditionally claimed. Instead we found that different proportions of phosphate species, which results in P/Al ratios higher than 1, arose during the genesis of the variscite deposits, modifying the concentrations of PO4 3–, H2PO4– and HPO4 2–. Thus, the P/Al atomic ratio should be an indication of provenance as it is established during mineral genesis.


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