FTFabienne Trolard
Fabienne Trolard
*This is an algorithmically generated author record based on publicly available information.
Research Subjects
Fabienne Trolard has a total of 72 co-authors. Here are the top co-authors by number of shared publications:
Guilhem Bourrié
Géochimie des sols et des eaux
11 shared publicationsG. Bourrié
INRA, UR 1119, Aix En Provence, France
6 shared publicationsMustapha Abdelmoula
4 shared publicationsPhilippe Refait
4 shared publicationsAlexander Neaman
3 shared publications- Frédéric Feder
CIRAD, UPR Recyclage et Risque, Montpellier, France
3 shared publications
Latest Publications
- Open Access
- 25 July 2012
- Published by Springer Nature in Environmental Earth Sciences
- Vol. 70 (5) , 2129-2141
Anthropogenic contamination of groundwater with nitrate in arid region: case study of southern Hodna (Algeria)
- 25 July 2012
- Published by Springer Nature in Environmental Earth Sciences
- Vol. 70 (5) , 2129-2141
Open AccessAnthropogenic contamination of groundwater with nitrate in arid region: case study of southern Hodna (Algeria)
- Top Cited PapersOpen Access
- 31 January 2012
- Published by Springer Nature in Agronomy for Sustainable Development
- Vol. 33 (2) , 291-309
Soil compaction impact and modelling. A review
- 31 January 2012
- Published by Springer Nature in Agronomy for Sustainable Development
- Vol. 33 (2) , 291-309
Top Cited PapersOpen AccessSoil compaction impact and modelling. A review
- 1 February 2011
- Published by Cambridge University Press (CUP) in Clays and Clay Minerals
- Vol. 59 (1) , 10-12
Reply to the Letter to the Editor by Christiansen, Dideriksen, Skovbjerg, Nedel, and Stipp: “On Fougerite”
- 1 February 2011
- Published by Cambridge University Press (CUP) in Clays and Clay Minerals
- Vol. 59 (1) , 10-12
Reply to the Letter to the Editor by Christiansen, Dideriksen, Skovbjerg, Nedel, and Stipp: “On Fougerite”
- 1 October 2009
- Published by Elsevier in Journal of Contaminant Hydrology
- Vol. 109 (1-4) , 27-39
Ionic contribution to the self-potential signals associated with a redox front
- 1 October 2009
- Published by Elsevier in Journal of Contaminant Hydrology
- Vol. 109 (1-4) , 27-39
Ionic contribution to the self-potential signals associated with a redox front
- 1 April 2008
- Published by Elsevier in Applied Geochemistry
- Vol. 23 (4) , 778-782
Trace element associations with Fe- and Mn-oxides in soil nodules: Comparison of selective dissolution with electron probe microanalysis
- 1 April 2008
- Published by Elsevier in Applied Geochemistry
- Vol. 23 (4) , 778-782
Trace element associations with Fe- and Mn-oxides in soil nodules: Comparison of selective dissolution with electron probe microanalysis
- 11 January 2008
- Published by Wiley in Geophysical Prospecting
- Vol. 56 (2) , 269-282
Redox potential distribution inferred from self‐potential measurements associated with the corrosion of a burden metallic body
- 11 January 2008
- Published by Wiley in Geophysical Prospecting
- Vol. 56 (2) , 269-282
Redox potential distribution inferred from self‐potential measurements associated with the corrosion of a burden metallic body
- 1 June 2007
- Published by Cambridge University Press (CUP) in Clays and Clay Minerals
- Vol. 55 (3) , 323-334
Fougerite, a new mineral of the pyroaurite-iowaite group: Description and crystal structure
Fougerite (IMA 2003-057) is a mixed M(II)-M(III) hydroxysalt of the green rust group, where M(II) can be Fe or Mg, and M(III) is Fe. The general structural formula is: where A is the interlayer anion and n its valency, with 1/4 ≼ x/(1+y) ≼ 1/3 and m ≼ (1−x+y). The structure of green rusts and parent minerals can accommodate a variety of anions, such as OH−, Cl−, ${\rm{CO}}_3^{2 - },\;{\rm{SO}}_4^{2 - }$ . The structure of the mineral was studied by Mössbauer, Raman and X-ray absorption spectroscopies (XAS) at the FeK edge. Mössbauer spectra of the mineral obtained at 78 K are best fitted with four doublets: D1 and D2 due to Fe2+ (isomer shift δ ≈ 1.27 and 1.25 mm s−1, quadrupole splitting ΔEQ ≈ 2.86 and 2.48 mm s−1, respectively) and D3 and D4 due to Fe3+ (δ ≈ 0.46 mm s−1, ΔEQ ≈ 0.48 and 0.97 mm s−1, respectively). Microprobe Raman spectra obtained with a laser at 514.53 nm show the characteristic bands of synthetic green rusts at 427 and 518 cm−1. X-ray absorption spectroscopy shows that Mg is present in the mineral in addition to Fe, that the space group is and the lattice parameter a ≈ 0.30–0.32 nm. The mineral forms by partial oxidation and hydrolysis of aqueous Fe2+, to give small crystals (400–500 nm) in the form of hexagonal plates. The mineral is unstable in air and transforms to lepidocrocite or goethite. The name is for the locality of the occurrence, a forested Gleysol near Fougères, Brittany, France. Its characteristic blue-green color (5BG6/1 in the Munsell system) has long been used as a universal criterion in soil classification to identify Gleysols. From a thermodynamic model of soil-solution equilibria, it was proposed that for the eponymous mineral, Fougères-fougerite, OH− may be the interlayer anion. In other environments, the interlayer anion may be different, and other varieties of fougerite may exist. Fougerite plays a key role in the pathways of formation of Fe oxides.- 1 June 2007
- Published by Cambridge University Press (CUP) in Clays and Clay Minerals
- Vol. 55 (3) , 323-334
Fougerite, a new mineral of the pyroaurite-iowaite group: Description and crystal structure
Fougerite (IMA 2003-057) is a mixed M(II)-M(III) hydroxysalt of the green rust group, where M(II) can be Fe or Mg, and M(III) is Fe. The general structural formula is: where A is the interlayer anion and n its valency, with 1/4 ≼ x/(1+y) ≼ 1/3 and m ≼ (1−x+y). The structure of green rusts and parent minerals can accommodate a variety of anions, such as OH−, Cl−, ${\rm{CO}}_3^{2 - },\;{\rm{SO}}_4^{2 - }$ . The structure of the mineral was studied by Mössbauer, Raman and X-ray absorption spectroscopies (XAS) at the FeK edge. Mössbauer spectra of the mineral obtained at 78 K are best fitted with four doublets: D1 and D2 due to Fe2+ (isomer shift δ ≈ 1.27 and 1.25 mm s−1, quadrupole splitting ΔEQ ≈ 2.86 and 2.48 mm s−1, respectively) and D3 and D4 due to Fe3+ (δ ≈ 0.46 mm s−1, ΔEQ ≈ 0.48 and 0.97 mm s−1, respectively). Microprobe Raman spectra obtained with a laser at 514.53 nm show the characteristic bands of synthetic green rusts at 427 and 518 cm−1. X-ray absorption spectroscopy shows that Mg is present in the mineral in addition to Fe, that the space group is and the lattice parameter a ≈ 0.30–0.32 nm. The mineral forms by partial oxidation and hydrolysis of aqueous Fe2+, to give small crystals (400–500 nm) in the form of hexagonal plates. The mineral is unstable in air and transforms to lepidocrocite or goethite. The name is for the locality of the occurrence, a forested Gleysol near Fougères, Brittany, France. Its characteristic blue-green color (5BG6/1 in the Munsell system) has long been used as a universal criterion in soil classification to identify Gleysols. From a thermodynamic model of soil-solution equilibria, it was proposed that for the eponymous mineral, Fougères-fougerite, OH− may be the interlayer anion. In other environments, the interlayer anion may be different, and other varieties of fougerite may exist. Fougerite plays a key role in the pathways of formation of Fe oxides.- 1 March 2007
- Published by Elsevier in Spectrochimica Acta Part B: Atomic Spectroscopy
- Vol. 62 (3) , 224-230
Application of direct solid analysis of plant samples by electrothermal vaporization-inductively coupled plasma atomic emission spectrometry: Determination of Cd and Si for environmental purposes
- 1 March 2007
- Published by Elsevier in Spectrochimica Acta Part B: Atomic Spectroscopy
- Vol. 62 (3) , 224-230
Application of direct solid analysis of plant samples by electrothermal vaporization-inductively coupled plasma atomic emission spectrometry: Determination of Cd and Si for environmental purposes