40 results on '"Lacalamita, M"'
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2. Armstrongite at non ambient conditions: An in-situ high temperature single crystal X-ray diffraction study
- Author
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Lacalamita, M., Cametti, G., Mesto, E., and Schingaro, E.
- Published
- 2019
- Full Text
- View/download PDF
3. Thermal stability and dehydration of armstrongite, a microporous zirconium silicate
- Author
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Schingaro, E., Lacalamita, M., Mesto, E., and Della Ventura, G.
- Published
- 2018
- Full Text
- View/download PDF
4. Refinement of the Crystal Structure of Vlasovite from Burpala Massif (Russia)
- Author
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Kaneva, E. V., Vladykin, N. V., Mesto, E., Lacalamita, M., Scordari, F., and Schingaro, E.
- Published
- 2018
- Full Text
- View/download PDF
5. In situ high-temperature XRPD and FTIR study of melanterite
- Author
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Lacalamita M., Ventruti G., Della Ventura G., Radica F., Mauro D., Schingaro E., Lacalamita, M., Ventruti, G., Della Ventura, G., Radica, F., Mauro, D., and Schingaro, E.
- Published
- 2021
6. XRD, micro-XANES, EMPA, and SIMS investigation on phlogopite single crystals from Mt. Vulture (Italy)
- Author
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Scordari, F., Dyar, M.D., Schingaro, E., Lacalamita, M., and Ottolini, L.
- Subjects
Lattice dynamics -- Research ,Phyllosilicates -- Properties ,X-ray spectroscopy -- Methods ,Earth sciences - Abstract
Selected phlogopite flakes from Mt. Vulture in southern Italy were studied using a combination of single-crystal techniques: electron microprobe analysis (EMPA), secondary ion mass spectrometry (SIMS), single-crystal X-ray diffraction (SCXRD), and micro-X-ray absorption near-edge spectroscopy (XANES). The latter technique was employed to analyze the structure of the Fe-K absorption edge over the region from 7080-8100 eV and to determine [Fe.sup.3+]/[ZIGMA]Fe at a micrometer scale, albeit with large error bars due to known effects of orientation on pre-edge energy. The annite component, Fe/(Mg+Fe), of the samples studied ranged from 0.16 to 0.31, the Ti content from 0.11 to 0.27 atoms per formula unit (apfu) and the Ba content from 0.03 to 0.09 apfu. SIMS analysis showed [H.sub.2]O (wt%) = 1.81-3.30, F (wt%) = 0.44-1.29, and [Li.sub.2]O (wt%) = 0.001-0.027. The intra single-crystal chemical variability for major/minor elements (Mg, Fe, Al, Ba, Ti, and K) was found particularly significant for samples VUT 191_11 and PG5_1, less significant for the other samples of the set. SIMS data relative to crystals VUT187_24, VUT191 10, VUT191_ll, and VUT187_28 showed a noteworthy variation in the concentrations of some light elements (H, Li, and F) with coefficient of variation CV (as l[sigma]%) up to ~18% for [H.SUB.2]O. The analyzed micas belong to the 1M polytype. Structure refinements using anisotropic displacement parameters were performed in space group C2/m and converged at 3.08 [less than or equal to] R [less than or equal to] 3.63, 3.32 [less than or equal to] [R.sub.w] [less than or equal to] 3.98%. Micro-XANES results yielded [Fe.sup.3+]/[ZIGMA]Fe from 51-93%. Previous Mossbauer data from powdered samples suggested [Fe.sup.3+]/[ZIGMA]Fe values ranging from 49-87%. However, the [Fe.Sup.3+] content determined by both techniques is sometimes remarkably different, in part because of the large errors ([+ or -] 10-15%) presently associated with the micro-XANES technique and in part because the [Fe.Sup.3+] content of a single crystal may significantly depart from the average value obtained from routine M6ssbauer analysis. The combination of EMPA, SIMS, and micro-XANES resulted in the characterization of the samples at a comparable spatial scale. By means of in-situ data and the results of crystallographic investigations, the occurrence of different relative amounts of [M.sup.3+]-oxy [[sup.VI][M.sup.2+] + [(OH).sup.-] [left and right arrow] [sup.VI][M.sup.3+] + [O.sup.2-] + 1/2 [H.sub.2][up arrow]], Ti-oxy substitutions [[sup.VI][M.sup.2+] + 2[(OH).sup.-] [left and right arrow] [sup.VI][Ti.sup.4+] + 2[O.sup.2-] + [H.sub.2][up arrow], and Ti-vacancy ([??]) substitution (2[sup.VI][M.sup.2+] [left and right arrow][sup.VI][Ti.sup.4+] + [sup.VI][??]) was ascertained for the studied samples. Keywords: Volcanic phlogopite, micro-XANES, SIMS, crystal chemistry, substitution mechanisms DOI: 10.2138/am.2010.3442
- Published
- 2010
7. Crystal-chemistry and vibrational (FTIR, Raman) spectroscopy of ferrinatrite, Na3[Fe3(SO4)3].3H2O, and its high-temperature decomposition
- Author
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VENTRUTI, Gennaro, Della Ventura, G., Sbroscia, M., Sodo, A., Lacalamita, M., Plaisier, J., Schingaro, E., Ventruti, Gennaro, Della Ventura, G., Sbroscia, M., Sodo, A., Lacalamita, M., Plaisier, J., and Schingaro, E.
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- 2018
8. Fluorophlogopite-bearing and carbonate 1 metamorphosed xenoliths from the Campanian Ignimbrite (Fiano, southern Italy): crystal chemical, geochemical and volcanological insights
- Author
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Lacalamita, M., BALASSONE, GIUSEPPINA, Schingaro, E., Mesto, E., Mormone, A., Piochi, M., Ventruti, G., Joachimski M., Lacalamita, M., Balassone, Giuseppina, Schingaro, E., Mesto, E., Mormone, A., Piochi, M., Ventruti, G., and Joachimski, M.
- Subjects
Fiano xenoliths, Campanian Ignimbrite, Southern Italy, fluorophlogopite, crystal chemistry, geochemistry - Abstract
Fluorine-, boron-, and magnesium-rich metamorphosed xenoliths occur in the Campanian Ignimbrite (CI) deposits at Fiano (southern Italy), at about 50 km northeast of the sourced volcanic area. These rocks originated from Mesozoic limestones of the Campanian Apennines, embedded in a fluid flow. The studied Fiano xenoliths consist of ten fluorophlogopite-bearing calc-silicate rocks and five carbonate xenoliths, characterized by combining mineralogical analyses with whole rock and stable isotope data. The micaceous xenoliths are composed of abundant idiomorphic fluorophlogopite, widespread fluorite, F-rich chondrodite, fluoborite, diopside, Fe(Mg)-oxides, calcite, humite, K-bearing fluoro-richterite and grossular. Out of the five mica-free xenoliths, two are calcite marbles, containing very subordinate fluorite and hematite, and three are weakly meamorphism carbonates, composed of calcite only. The crystal structure and chemical composition of fluorophlogopite approach those of the end member. The Fiano xenoliths are enriched in trace elements with respect to the primary limestones. Comparison between the REE patterns of the Fiano xenoliths and those of both CI and Somma-Vesuvius marble and carbonate xenoliths shows that the Fiano pattern on the whole both overlaps that of Somma-Vesuvius marble and carbonate xenoliths, and yet reproduces the trend of CI rocks. δ13C and δ18O values depict the same trend of depletion in the heavy isotopes observed in the Somma-Vesuvius nodules, related tothermometamorphism. Trace element distribution, paragenesis, stable isotope geochemistry and data modelling point to infiltration of steam enriched in F, B, Mg, As into carbonate rocks at temperature of ca. 300-450°C during the emplacement of the CI.
- Published
- 2017
9. Fluorophlogopite and F-rich phases in limestone clasts from the Campanian Ignimbrite quarried at Fiano (southern Italy): mineralogical, geochemical and volcanological insights
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LACALAMITA M., SCHINGARO E., MESTO E., SCORDARI F., MORMONE A., PIOCHI M., JOACHIMSKI M., BALASSONE, GIUSEPPINA, Cesare B., Erba E., Carmina B., Fascio L., Petti F.M., Zuccari A., Lacalamita, M., Balassone, Giuseppina, Schingaro, E., Mesto, E., Scordari, F., Mormone, A., Piochi, M., and Joachimski, M.
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Campanian Ignimbrite ,Southern Italy ,Fiano xenolith ,chemistry ,F(Mg)-rich mineral ,crystal - Abstract
Fluorine-rich metamorphosed xenoliths associated to the distal Campanian Ignimbrite (CI) tephra (Campania region, southern Italy) have long attracted the interest of the mineralogical community (i.e. Scacchi, 1890; Zambonini, 1919; Masi & Turi, 1972; Balassone et al., 2002). These rocks derive from the Mesozoic carbonate lithotypes of the Campanian Apennine, embedded in the pyroclastic flow and presently resting at the bottom of the tuff formations. The sedimentary protoliths suffered from the action of hot, volatile-rich pyroclastic flow, and consequently were affected by thermal metamorphism to various degrees. Their peculiarity is the occurrence of F- and Mg-bearing phases, with an ubiquitous presence of neoformed fluorite. The occurrence at Fiano quarries (the so-called “Tufare”) is the classical locality for these rock xenoliths. Similar rocks were also found in the CI of the Caserta area, and in the Latium region (Colli Albani). This research aims both at a crystal chemical study of fluorophlogopite occurring in the Fiano xenoliths, and at a geochemical and volcanological survey, to constrain the petrogenesis processes related to this rare F-, Mg-rich assemblage and to CI. The analysed samples belong to two lithotypes: mica-bearing clasts and variably metamorphosed carbonate blocks. The former lithotype is represented by abundant fluorite, followed by fluorophogopite, F-rich chondrodite, fluoborite, diopside and (Fe,Mg)-oxides. Minor to trace contents of calcite, humite, tremolite, and grossular also occur. Carbonate rocks can show calcite only, or also trace amounts of fluorite. The Fiano micas composition approaches that of the Vesuvius micas from the 1872 eruption (Balassone et al., 2013). The micas belong to the 1M polytype and have crystal chemical features typical of fluorophlogopites i.e., low c lattice parameter (~ 10.13 Å), (~ 2.060 Å) and (~ 3.135 Å) distances. New data on minor to ultratrace elements amounts found in the studied clasts, together with Carbon and Oxygen isotope data will be reported and interpreted in a petrogenetic and volcanological frame. Balassone G., Franco E., Mattia C.A., Petti C. & Puliti R. 2002. Re-examination of fluosiderite, an unknown mineral from southern Italy: equal to fluorine-rich chondrodite. Eur. J. Min., 14, 151-155. Balassone G., Scordari F., Lacalamita M., Schingaro E., Mormone A., Piochi M., Petti C. & Mondillo N. 2013. Trioctahedral micas in xenolithic ejecta from recent volcanism of the Somma-Vesuvius (Italy): crystal chemistry and genetic inferences. Lithos, 160-161, 84-97. Masi U. & Turi B. 1972. Frazionamento isotopico del carbonio e dell'ossigeno negli inclusi calcarei metamorfosati del "Tufo grigio campano" Auct. di Fiano (Salerno). Per. Min., 41, 291-310. Scacchi A. 1890. La regione vulcanica fluorifera della Campania. Mem. R. Com. Geol. It., I, 1-48. Zambonini F. 1919. Il tufo pipernoide della Campania e i suoi minerali. Mem. Descr. Carta Geol. It., 7, 130 pp.
- Published
- 2014
10. Ti-rich garnets: an EPMA, SIMS, MÖSSBAUER, XRPD and SCXRD investigation
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Schingaro E.1, Lacalamita M.*1, Mesto E.1, Ventruti G.1, Pedrazzi G.2, Ottolini L.3, and Scordari F.1
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multi-methodic approach ,Ti-bearing garnets ,crystal chemistry - Abstract
A suite of Ti-bearing garnets from magmatic, metamorphic and carbonatitic rocks was studied by Electron Probe Microanalysis (EPMA), X-ray Powder Diffraction (XRPD), Single Crystal X-ray Diffraction (SCXRD), Mössbauer spectroscopy and Secondary Ion Mass Spectrometry (SIMS) in order to better characterize their crystal chemistry. The studied garnets show TiO2 varying in the ranges 4.9(1)-17.1(2) wt.% and variable Fe3+/?Fe content. SIMS analyses allowed quantification of light elements yielding H2O in the range 0.091(7)-0.46(4), F in the range 0.004(1)-0.040(4) and Li2O in the range 0.0038(2)-0.014(2) wt%. Mössbauer analysis provided spectra with different complexity, which could be fitted to a number of components variable from one (YFe3+) to four (YFe2+, ZFe2+, YFe3+, ZFe3+). A good correlation was found between the Fe3+/?Fe resulting from the Mössbauer analysis and that derived from the Flank method (Höfer & Brey, 2007). X-ray powder analysis revealed that the studied samples are a mixture of different garnet phases with very close cubic unit cell parameters as recently found by other authors (Antao, 2013). Single crystal X-ray refinements using anisotropic displacement parameters were performed in the Ia-3d space group and converged to R1 in the range 1.63-2.06 % and wR2 in the range 1.44-2.21 %. Unit cell parameters vary between 12.0641(1) and 12.1447(1) Å, reflecting different Ti contents and extent of substitutions at tetrahedral site. The main substitution mechanisms affecting the studied garnets are: YR4+ + ZR3+ ZSi + YR3+ (schorlomite substitution); YR2+ + ZR4+ 2YR3+ (morimotoite substitution); YFe3+ YR3+ (andradite substitution) with ZR4+ = Ti; YR4+ = Ti, Zr; YR3+ = Fe3+, Al3+, Cr3+; ZR3+ = Fe3+, Al3+ and YR2+ = Fe2+, Mg2+, Mn2+. The 2YTi4++ ZFe2+ 2YFe3+ + ZSi4+, the hydrogarnet substitution [(SiO4)4- (O4H4)4-], the F- OH- and the YR4+ + XR+ YR3+ + XCa2+, with YR4+ = Ti, Zr; YR3+ = Fe3+, Al3+, Cr3+; XR+ = Na, Li also occur. The garnet crystal chemistry and implications in terms of nomenclature and classification (Grew et al., 2013) are discussed. Antao S.M. 2013. The mystery of birefringent garnet: is the symmetry lower than cubic?. Powder diffr., 28(4), 281-287. Grew E.S., Locock A.J., Mills S.J., Galuskina I.O., Galuskina E.V. & Hålenius U. 2013. Nomenclature of the Garnet Supergroup. Am. Mineral., 98, 785-811. Höfer H.E. & Brey G.P. 2007. The iron oxidation state of garnet by electron microprobe: Its determination with the flank method combined with major-element analysis. Am. Mineral., 92, 873-885.
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- 2015
11. Hydrogen, fluorine and lithium investigation in hydrogarnets by Secondary Ion Mass Spectrometry: Comparison with X-ray and spectroscopic techniques
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OTTOLINI L.P. 1, SCORDARI F. 2, SCHINGARO E. 2, and LACALAMITA M. 2
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Secondary Ion Mass Spectrometry ,hydrogarnets ,spectroscopic techniques ,light and volatile elements ,X-ray diffraction - Abstract
The incorporation of OH- in trace but measurable amounts in the structure of nominally anhydrous minerals is to date well documented. OH- occurring in this manner may constitute the dominant reservoir of hydrogen in the Earth's interior and is believed to play an important role in the physical properties of the mantle. It may also affect the evolution of the hydrosphere through its influence on mantle melting and isotopic fractionation [1]. In Ti-garnets, hydrogen may be incorporated via the hydrogarnet substitution, where a SiO4 unit may locally be replaced by a H4O4-tetrahedron. However, more complex mechanisms have also been proposed [2]. In addition, the uptake of fluorine into the structure is more complex than the simple exchange reaction F- OH- [3]. In this study, Secondary Ion Mass Spectrometry (SIMS) has been used to analyse hydrogen -quantified conventionally as H2O (wt%)-, fluorine and lithium in a suite of Ti garnets of different origin and geological provenance. From Electron Probe Micro-Analysis (EPMA) and structure refinements from single crystal X-ray diffraction (SCXRD) data, such garnets were expected to have tetrahedral substitutions and a hydrogarnet component. FTIR preliminary spectra in the OH- stretching region evidenced that, comparatively, the samples were characterized by various degrees of hydration. The results of our SIMS analyses confirmed the presence of significant amount of H2O (0.091 - 0.459 wt%), low concentration of F (0.0089 - 0.048 wt%) as well as of Li2O (0.0024 - 0.0139 wt%). The comparison with data obtained by X-ray site scattering refinement and Mössbauer spectroscopy allowed to ascertain that the combination of VITi4+VIM3+-1 IVFe3+IVSi-1 (schorlomite substitution) and VIM2+VITi4+VIFe3+-2 (morimotoite substitution), with M3+ = Fe3+, Al3+, and M2+ = Fe2+, Mg2+, Mn2+, can explain most of the chemical variation of tetrahedral and octahedral sites. However, the accurate evaluation of H and F by SIMS favoured the assessment of minor substitution mechanisms. A good qualitative agreement between SIMS and FTIR data was found.
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- 2011
12. O13 Efficacy and safety of sofosbuvir/velpatasvir in people with chronic hepatitis C virus infection and recent injecting drug use: the SIMPLIFY study
- Author
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Grebely, J., Dalgard, O., Conway, B., Cunningham, E., Bruggmann, P., Hajarizadeh, B., Amin, J., Marks, P., Quiene, S., Applegate, T.L., Swan, T., Byrne, J., Lacalamita, M., Dunlop, A., Bruneau, J., Hellard, M.E., Matthews, G.V., Powis, J., Shaw, D., Thurnheer, M.C., Weltman, M., Kronborg, I., Cooper, C., Feld, J.J., Fraser, C., Litwin, A., Dillon, J., Read, P., Gane, E., and Dore, G.J.
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- 2017
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13. Multi-analytical characterization of NH4+ bearing phlogopites from Mt. Vulture (Italy)
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LACALAMITA M. (1), SCHINGARO E. (1), SCORDARI F. (1), VENTRUTI G. (1), and OTTOLINI L. (2)
- Published
- 2007
14. Multimethodic approach to the crystal chemistry of Ti-rich phologopites from Mt. Vulture (Potenza, Italy)
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Lacalamita M., Schingaro E., Scordari F., Ventruti G., and Ottolini L.
- Published
- 2006
15. Fluorophlogopite-bearing and carbonate metamorphosed xenoliths from theCampanian Ignimbrite (Fiano, southern Italy): crystal chemical, geochemical and volcanological insights.
- Author
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LACALAMITA, M., BALASSONE, G., SCHINGARO, E., MESTO, E., MORMONE, A., PIOCHI, M., VENTRUTI, G., and JOACHIMSKI, M.
- Subjects
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INCLUSIONS in igneous rocks , *IGNIMBRITE , *CRYSTAL structure , *VOLCANOLOGY , *GEOCHEMISTRY , *MINES & mineral resources - Abstract
Fluorine-, boron- and magnesium-rich metamorphosed xenoliths occur in the Campanian Ignimbrite deposits at Fiano (southern Italy), at ~50 km northeast of the sourced volcanic area. These rocks originated from Mesozoic limestones of the Campanian Apennines, embedded in a fluid flow. The Fiano xenoliths studied consist of ten fluorophlogopite-bearing calc-silicate rocks and five carbonate xenoliths, characterized by combining mineralogical analyses with whole-rock and stable isotope data. The micaceous xenoliths are composed of abundant idiomorphic fluorophlogopite, widespread fluorite, F-rich chondrodite, fluoborite, diopside, Fe(Mg)-oxides, calcite, humite, K-bearing fluoro-richterite and grossular. Of the five mica-free xenoliths, two are calcite marbles, containing subordinate fluorite and hematite, and three are weakly metamorphosed carbonates, composed only of calcite. The crystal structure and composition of fluorophlogopite approach that of the end-member. The Fiano xenoliths are enriched in trace elements with respect to the primary limestones. Comparisons between the rare-earth element (REE) patterns of the Fiano xenoliths and those of both Campanian Ignimbrite and Somma-Vesuvius marble and carbonate xenoliths showthat the Fiano pattern overlaps that of Somma-Vesuvius marble and carbonate xenoliths, and reproduces the trend of Campanian Ignimbrite rocks. Values of δ13C and δ18O depict the same trend of depletion in the heavy isotopes observed in the Somma-Vesuvius nodules, and is related to thermometamorphism. Trace-element distribution, paragenesis, stable isotope geochemistry and data modelling point to infiltration of steam enriched in F, B,Mg and As into carbonate rocks at a temperature of ~300-450°C during the emplacement of the Campanian Ignimbrite. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
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16. Structure refinement and crystal chemistry of tokkoite and tinaksite from the Murun massif (Russia).
- Author
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Lacalamita, M., Mesto, E., Kaneva, E., Scordari, F., Pedrazzi, G., Vladykin, N., and Schingaro, E.
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SINGLE crystals , *MOLECULAR structure , *X-ray diffraction , *MOSSBAUER effect - Abstract
The structures of tokkoite, K2Ca4[Si7O18OH](OH,F) and tinaksite, K2Ca2NaTi[Si7O18OH]O from the Murun massif (Russia) were refined from single-crystal X-ray diffraction data in the triclinic space group P1̄: Average crystallographic data are a ≈ 10.423, b ≈ 12.477, c ≈ 7.112 Å, α ≈ 89.92°, β ≈ 99.68°, γ ≈ 92.97°, V ≈ 910.5 Å3 for tokkoite; a ≈ 10.373, b ≈ 12.176, c ≈ 7.057 Å, α ≈ 90.82°, β ≈ 99.22°, γ ≈ 92.80°, V ≈ 878.5 Å3 for tinaksite. The substantial similarities between the geometrical parameters of the tokkoite and tinaksite structures led us to conclude that the two minerals are isostructural. However, major differences of tokkoite with respect to tinaksite are larger lattice constants, especially concerning the b parameter, longer
distances, especially ; larger values of the M1-M3 and O20-O2 bond lengths, and a stronger distortion of the M1 polyhedron. Mössbauer analysis showed that significant trivalent iron is present, VIFe3+ 40.0(7)% in tokkoite and 12.8(3)% in tinaksite. It is confirmed that 2Ca(M1+M2)2+ + (F, OH)-(O20) ↔ Ti4+(M1) +Na+(M2) +O-(O20) is the exchange reaction that describes the relation between tokkoite and tinaksite. In addition, this exchange reaction causes local stress involving mainly the M1 site and its interaction with the M2 and M3 sites. [ABSTRACT FROM AUTHOR] - Published
- 2017
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17. Single-crystal X-ray diffraction, EMPA, FTIR and X-ray photoelectron spectroscopy study of narsarsukite from Murun Massif, Russia.
- Author
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Schingaro, E., Mesto, E., Lacalamita, M., Scordari, F., Kaneva, E., and Vladykin, F. N.
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- 2017
- Full Text
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18. FRI-234 - Efficacy and safety of sofosbuvir/velpatasvir in people with chronic hepatitis C virus infection and recent injecting drug use: the SIMPLIFY study
- Author
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Grebely, J., Dalgard, O., Conway, B., Cunningham, E., Bruggmann, P., Hajarizadeh, B., Amin, J., Marks, P., Quiene, S., Applegate, T.L., Swan, T., Byrne, J., Lacalamita, M., Dunlop, A.J., Bruneau, J., Hellard, M.E., Matthews, G.V., Powis, J., Shaw, D., Thurnheer, C.M., Weltman, M., Kronborg, I., Cooper, C., Feld, J.J., Fraser, C., Litwin, A., Dillon, J., Read, P., Gane, E., and Dore, G.J.
- Published
- 2017
- Full Text
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19. Structural anomalies in tobelite-2M2 explained by high resolution and analytical electron microscopy.
- Author
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CAPITANI, G. C., SCHINGARO, E., LACALAMITA, M., MESTO, E., and SCORDARI, F.
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- 2016
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20. Morphological and mineralogical characterization of surficial weathering on calcarenite rocks in the rupestrian system of "San Michele delle Grotte" at Gravina in Puglia (Bari, Apulia).
- Author
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D'Angeli, I.M., Lacalamita, M., Sasso, C., Schingaro, E., and Parise, M.
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WEATHERING , *X-ray powder diffraction , *PETROGRAPHIC microscope , *EFFLORESCENCE , *SCANNING electron microscopy - Abstract
• Unaltered and weathered samples of Calcarenite di Gravina were analyzed. • Biological colonizations and efflorescences cover the surface of calcarenite. • Biological colonizations are dominated by algae covering the calcarenite substrate. • Efflorescences contain mainly sulfates and other salts including niter and sylvine. • Salt weathering may originate from anthropic activity or environmental factors. San Michele delle Grotte is a rupestrian cave excavated into the "Calcarenite di Gravina" formation, resting over the Cretaceous formation of "Calcare di Altamura". Both rock types show evident instability features and intense surficial rock weathering. A detailed mineralogical and morphologic characterization of Calcarenite di Gravina Fm. samples has been carried out by means of optical and petrographic microscope (OM and PM), scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). In thin section, bioclastic packstone to grainstone fabrics were observed. In the surficial portion of the rock it is possible to find biological colonizations and efflorescences: the first are dominated by algae covering the calcite substrate, whilst the efflorescences contain mainly sulfates such as syngenite, gypsum and arcanite, and other salts including niter and sylvine. A distinctive enhance of microporosity on the rock surface immediately at the contact with the biological colonizations and efflorescences was observed. A high abundance of biological colonizations was found where the hostrock is well exposed to light, whereas efflorescences prevail in the innermost parts of the cavity. Efflorescences may originate from both anthropogenic air pollution (wet and dry airborne deposition that provides sulfate and nitrate anions) and circulation of soil water whose composition can be modified, for instance, by fertilizers. Analysis of the weathering conditions of calcarenite rocks is a crucial factor in determining the likely possibility of failures and collapses in underground environments. [ABSTRACT FROM AUTHOR]
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- 2022
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21. Substitution mechanisms and implications for the estimate of water fugacity for Ti-rich phlogopite from Mt. Vulture, Potenza, Italy.
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LACALAMITA, M., SCHINGARO, E., SCORDARI, F., VENTRUTI, G., FABBRIZIO, A., and PEDRAZZI, G.
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CRYSTALS , *SPECTRUM analysis , *CRYSTALLOGRAPHY , *FOURIER transform infrared spectroscopy - Abstract
The crystal chemistry of Ti-rich phlogopite from deposits of the oldest activity (~740 ka) of Mt. Vulture, Potenza, Italy, was investigated to identify the substitution mechanisms in Ti-rich phlogopite and to determine its potential as a geohygrometer. Substitution mechanisms were determined by electron probe microanalysis (EPMA), single-crystal X-ray diffraction (SCXRD), Mössbauer spectroscopy, and micro-Fourier transform infrared (FTIR) spectroscopy. Magnetite and sanidine from the mica-rich host rocks were also analyzed. Use of the biotite-magnetite-sanidine geohygrometer in these volcanics (essentially trachytic-phonolitic ignimbrites) is exploited. All investigated phlogopite samples consist of the 1M polytype, with 5.3275(2) ≤ a ≤ 5.3635(4) Å, 9.2211(4) ≤ b ≤ 9.2958(8) Å, 10.1211(5) ≤ c ≤ 10.281(1) Å, and 99.980(3) ≤ β ≤ 100.097(2)°. Structure refinements in space group C2/m converged to 2.42 ≤ R1 ≤ 4.00% and 2.04 ≤ wR2 ≤ 4.50%. VIFe3+ /Fetot from Mössbauer analyses ranged from 34(1)-89(1)%. The main bands in the OH-stretching region are 3709, 3682, and 3658 cm-1, and were assigned to 3Mg-OH--K-OH , 3Mg-OH--K-O2-, and 2MgFe3+ - OH--K-O2- local configurations, respectively. The overall crystal chemical features are compatible with the M3+-Tschermak substitutions (VIM2+ + IVSi4 ↔ VIM3+ + IVAl, with M3+ = Al, Fe3+), M3+-oxy [VIM2+ + (OH)- ↔ M3+ + (O) 2- + 1/2H2↑ and Ti-oxy substitutions [VIM2+ + 2(OH)-1 → VITi4+ + 2(O)2- + H2↑]. The magnetite composition varies between Mt82Uv18 and Mt93Uv07, whereas the proportion of orthoclase with respect to albite plus anorthite is 0.77 ≤ XOr =≤ 0.82. A partly ionic model was used to estimate annite activity, starting from experimentally determined substitutions in phlogopite. The resulting water fugacity was an order of magnitude lower than that calculated using stoichiometry to determine the phlogopite formula. The results are consistent with the occurrence of a well-developed hydrothermal system that altered the magmatic oxygen fugacity conditions at Mt. Vulture. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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22. Crystal chemistry of Ti-rich fluorophlogopite from Presidente Olegario, Alto Paranaíba igneous province, Brazil.
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SCHINGARO, E., LACALAMITA, M., SCORDARI, F., BRIGATTI, M. F., and PEDRAZZI, G.
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ELECTRON probe microanalysis , *MICROPROBE analysis , *MOSSBAUER spectroscopy , *SPECTRUM analysis , *CATIONS - Abstract
Trioctahedral micas from kamafugitic lavas of Presidente Olegario (Brazil) are Ti-Fe-bearing fluorophlogopites. They were investigated using a combination of electron probe microanalysis (EPMA), single-crystal X-ray diffraction (SCXRD), and Mössbauer spectroscopy. EPMA data yielded the following ranges: Al2O3 (8.7-10.1 wt%), MgO (19.6-20.6 wt%), FeO (5.7-6.5 wt%), TiO2 (5.9-7.5 wt%), K2O (8.9-9.7 wt%), Na2O (0.4 -0.6 wt%), and fluorine (3.4-4.1 wt%). Mössbauer investigation indicated: VIFe2+ ~ 60%, VIFe3+ ~ 10%, IVFe3+ ~ 30%. X-ray analysis indicated the 1M polytype, with cell parameters in the range a = 5.3208-5.3376, b = 9.2210-9.2464, c= 10.1227-10.155 Å, β= 100.157-100.194°. Structure refinements using anisotropic displacement parameters were performed in space group C2/m and converged to 2.01 ≤ R1 ≤ 3.51,2.00 ≤ wR2 ≤ 3.51%. The micas have no VIAl3+ and Na is probably partitioned over both interlayer and octahedral sites. Major substitutions are OH- ↔ F-, and the Ti-oxy substitution: VIM2+ + 2(OH)- ↔ VITi4+ + 2O2- + H2↑. Accordingly, the structural features of the studied micas encompass those typical of both fluorophlogopites and micas affected by Ti-oxy substitution. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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23. P.13.15 CHARACTERISTICS, HOSPITALIZATION AND MORTALITY OF PATIENTS WITH GI BLEEDING ADMITTED TO ALL EMERGENCY DEPARTMENTS OF THE LAZIO REGION
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Franceschi, F., Alessandra, B., Quadrino, F., Lacalamita, M., Buccelletti, F., Baiocchi, L., Cesaro, P., Gigliozzi, A., Antonietta, L., Gasbarrini, A., Silveri, N. Gentiloni, Kohn, A., Petruzziello, L., Angelico, M., and Tammaro, L.
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- 2012
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24. The role of SIMS in the investigation of the complex crystal chemistry of mica minerals.
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Ottolini, L. P., Schingaro, E., Scordari, F., Mesto, E., and Lacalamita, M.
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- 2010
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25. Using a natural chlorite as catalyst in chemical recycling of waste plastics: Hydrolytic depolymerization of poly-[bisphenol A carbonate] promoted by clinochlore
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Cosimino Malitesta, Ernesto Mesto, Enrico Scelsi, Eugenio Quaranta, Emanuela Schingaro, Maria Lacalamita, Elisabetta Mazzotta, Quaranta, E., Mesto, E., Lacalamita, M., Malitesta, C., Mazzotta, E., Scelsi, E., and Schingaro, E.
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Bisphenol A ,Carbonate ,020209 energy ,Carbonates ,02 engineering and technology ,010501 environmental sciences ,Plastic ,01 natural sciences ,Poly-[bisphenol A carbonate] ,Chloride ,Catalysis ,Hydrolysis ,chemistry.chemical_compound ,Chlorides ,Phenols ,0202 electrical engineering, electronic engineering, information engineering ,Recycling ,Benzhydryl Compounds ,Waste Management and Disposal ,Tetrahydrofuran ,0105 earth and related environmental sciences ,Benzhydryl Compound ,Phenol ,Depolymerization ,Hydrolysi ,Waste valorization ,Solvent ,Monomer ,chemistry ,Chemical engineering ,Clinochlore ,Plastics ,Chlorite ,Plastics chemical recycling - Abstract
The present study describes the first example of utilization of a natural clay mineral as catalyst in a process addressed to chemical valorization of poly-[bisphenol A carbonate] (PC; (1)) wastes. A natural clinochlore was investigated for the first time as the catalyst of the hydrolysis reaction of 1, a potential route to chemical recycling of wastes of this polymeric material. At 473 K, in tetrahydrofuran (THF) as the solvent, the mineral promoted effectively the depolymerization (up to 99%, after 6 h) of 1 by H2O and the selective (~99%) regeneration of the monomer bisphenol A (BPA, (2)). Temperature, catalyst loading, reaction time, H2O/PC weight ratio affected markedly the productivity of the process. The role of the catalyst was also focused: the experimental data showed that the exposed brucite-like sheets of clinochlore are involved in the hydrolysis reaction and take active part in promoting the depolymerization process.
- Published
- 2021
26. Crystal Chemistry and Luminescence Properties of Eu-Doped Polycrystalline Hydroxyapatite Synthesized by Chemical Precipitation at Room Temperature
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Giovanni Bruno, Dritan Siliqi, Francesco Capitelli, Maria Lacalamita, Francesco Baldassarre, Alberto Sacchetti, Nicola Corriero, Ernesto Mesto, Bujar Dida, Dafina Karaj, Angela Altomare, Giancarlo Della Ventura, Baldassarre, F., Altomare, A., Corriero, N., Mesto, E., Lacalamita, M., Bruno, G., Sacchetti, A., Dida, B., Karaj, D., Della Ventura, G., Capitelli, F., and Siliqi, D.
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Materials science ,Photoluminescence ,General Chemical Engineering ,Analytical chemistry ,chemistry.chemical_element ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Inorganic Chemistry ,symbols.namesake ,chemical precipitation method ,lcsh:QD901-999 ,General Materials Science ,Fourier transform infrared spectroscopy ,europium ,Rietveld refinement ,hydroxyapatite ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,0104 chemical sciences ,PXRD ,FTIR ,Raman and PL spectroscopy ,chemistry ,symbols ,Crystallite ,lcsh:Crystallography ,0210 nano-technology ,Luminescence ,Europium ,Raman spectroscopy ,Powder diffraction - Abstract
Europium-doped hydroxyapatite Ca10(PO4)6(OH)2 (3% mol) powders were synthesized by an optimized chemical precipitation method at 25 °, C, followed by drying at 120 °, C and calcination at 450 °, C and 900 °, C. The obtained nanosized crystallite samples were investigated by means of a combination of inductively coupled plasma (ICP) spectroscopy, powder X-ray diffraction (PXRD), Fourier Transform Infrared (FTIR), Raman and photoluminescence (PL) spectroscopies. The Rietveld refinement in the hexagonal P63/m space group showed europium ordered at the Ca2 site at high temperature (900 °, C), and at the Ca1 site for lower temperatures (120 °, C and 450 °, C). FTIR and Raman spectra showed slight band shifts and minor modifications of the (PO4) bands with increasing annealing temperature. PL spectra and decay curves revealed significant luminescence emission for the phase obtained at 900 °, C and highlighted the migration of Eu from the Ca1 to Ca2 site as a result of increasing calcinating temperature.
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- 2020
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27. The speciation of thallium in (Tl,Sb,As)-rich pyrite
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Elena Bonaccorsi, Giovanna Agrosì, Francesco d'Acapito, Cristian Biagioni, Giovanni Orazio Lepore, Luke L. George, Gian Carlo Capitani, Maria Lacalamita, George, L, Biagioni, C, Lepore, G, Lacalamita, M, Agrosì, G, Capitani, G, Bonaccorsi, E, and D'Acapito, F
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Absorption spectroscopy ,XAS ,020209 energy ,Coordination number ,Metamorphic rock ,Geochemistry ,Analytical chemistry ,chemistry.chemical_element ,02 engineering and technology ,engineering.material ,010502 geochemistry & geophysics ,Mass spectrometry ,01 natural sciences ,thallium ,Geochemistry and Petrology ,0202 electrical engineering, electronic engineering, information engineering ,LA-ICP-MS ,0105 earth and related environmental sciences ,X-ray absorption spectroscopy ,Geology ,pyrite ,Pyrite ,Speciation ,TEM ,Thallium ,chemistry ,speciation ,Transmission electron microscopy ,engineering ,Economic Geology - Abstract
Three samples of (Tl,Sb,As)-rich pyrite from the ore deposits of the southern Apuan Alps (Tuscany, Italy) were studied through a multi -technique approach in order to constrain the speciation and incorporation mechanism of thallium in pyrite. High concentrations of TI, Sb, and As were detected in all the studied samples through laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS). Average Tl contents were 1299 ppm, 1967 ppm, and 2623 ppm in samples from Sennari, Canale della Radice, and Fornovolasco, respectively. The LA-ICP-MS time-resolved down-hole ablation profiles were smooth indicating that TI, Sb, and As are dissolved in the pyrite matrix, or occur in homogeneously distributed nanoparticles (NPs). X-ray absorption spectroscopy (XAS) data revealed that Tl, Sb, and As occurs as Tl+, Sb3+, As3+, and As In all the studied samples, bond distances and coordination numbers for Sb3+ and Asa" are constant, whereas Tl displays a range of coordination numbers (similar to 3 to similar to 6), revealing the occurrence of different local environments. Moreover, no hints of features corresponding to coordination shells higher than the first were observed, suggesting an extremely disordered environment around Tl. Transmission electron microscopy (TEM) investigations revealed the presence of dislocations and As -rich "fluid" inclusions, whereas no Tl-rich NPs were observed. The study suggests that Tl+ could occur in structural defects in pyrite, lacking any long-range order. The 'loose' nature of TI in pyrite favours its ready loss during the metamorphic recrystallization of pyrite and its redistribution within ore bodies and country rocks, with important implications from an economic and environmental point of view.
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- 2019
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28. Trioctahedral micas in xenolithic ejecta from recent volcanism of the Somma-Vesuvius (Italy): Crystal chemistry and genetic inferences
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Nicola Mondillo, Emanuela Schingaro, Angela Mormone, Fernando Scordari, Giuseppina Balassone, Carmela Petti, Maria Lacalamita, Monica Piochi, Balassone, Giuseppina, Scordari, F., Lacalamita, M., Schingaro, E., Mormone, A., Piochi, M., Petti, C., and Mondillo, Nicola
- Subjects
Metamorphic rock ,Somma-Vesuviu ,Geochemistry ,trioctahedral mica ,Geology ,Skarn ,engineering.material ,Geochemistry and Petrology ,Magma ,engineering ,Phlogopite ,Xenolith ,Essexite ,crystal chemistry ,Metasomatism ,Mafic ,genetic inferences - Abstract
This study reports the first crystal chemical database resulting from a detailed structural investigation of trioctahedral micas found in xenolithic ejecta produced during the AD 1631, 1872 and 1944 eruptions, three explosive episodes of recent volcanic period of Vesuvius volcano (Southern Italy). Three xenolith types were selected: metamorphic/metasomatic skarns, pyrometamorphic/hydrothermally altered nodules and mafic cumulates. They are related to different magma chemistry and effusive styles: from sub-plinian and most evolved (AD 1631 eruption) to violent strombolian with medium evolution degree (AD 1872 eruption) to vulcanian-effusive, least evolved (AD 1944 eruption) event, respectively. Both xenoliths and micas were investigated employing multiple techniques: the xenoliths were characterized by X-ray fluorescence, inductively-coupled plasma-mass spectrometry, optical microscopy, X-ray powder diffraction, and quantitative energy-dispersive microanalysis; the micas were studied by electron probe microanalysis and single crystal X-ray diffraction, The mica-bearing xenoliths show variable texture and mineralogical assemblage, clearly related to their different origin. Based on the major oxide chemistry, only one xenolithic sample falls in the skarn compositional field from the Somma-Vesuvius literature, some fall close to the skarns and cumulate fields, others plot close to the syenite/foidolite/essexite field. A subgroup of the selected ejecta does not fall or approach any of the compositional fields. Trace and rare earth element patterns show some petrological affinity between studied xenoliths and erupted magmas with typical Eu, Ta and Nb negative anomalies. Strongly depleted patterns were detected for the 1631 metamorphic/metasomatic skarns xenoliths. Three distinct mica groups were distinguished: 1) Mg-, Al-rich, low Ti-bearing, low to moderate F-bearing varieties (1631 xenolith), 2) Al-moderate, F- and Mg-rich, Ti-, Fe-poor varieties (1872 xenolith), and 3) Al-, Ti- and Fe-rich, F-poor phases (1944 xenolith). All the analyzed mica crystals are 1M polytypes with the expected space group C2/m. Micas from xenoliths of the 1631 Vesuvius eruption are phlogopites characterized by a combination of low extent of oxy-type and variable extent OH- --> F- substitutions, as testified by the range of F concentration (from similar to 0.20 to 0.80 apfu). Micas from xenoliths of the 1872 Vesuvius eruption exhibit structural peculiarities typical of fluorophlogopites, i.e. OH- --> F- substitution is predominant. Micas from the xenolith of the 1944 Vesuvius eruption display features typical of oxy-substituted micas. The variability of the crystal chemical features of the studied micas is consistent with the remarkable variation of their host rocks. Micas from 1631 nodules are related to metasomatic, skarn-type environment, deriving from the metamorphosed wall-rocks hosting the magma reservoir. The fluorophlogopites from the 1872 xenoliths testify for strongly dehydrated environmental conditions compared to those of the 1631 and 1944 hosts. Finally, magma storage condition at depth, associated to a decreasing a(H2O) may have promoted major oxy-type substitutions in 1944 biotites.
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- 2013
29. Microplastics in inland and offshore sediments in the Apulo-Lucanian region (Southern Italy).
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Cofano V, Mele D, Lacalamita M, Di Leo P, Scardino G, Bravo B, Cammarota F, and Capolongo D
- Subjects
- Plastics, Geologic Sediments chemistry, Environmental Monitoring methods, Microplastics chemistry, Water Pollutants, Chemical analysis
- Abstract
Inland and offshore sediments from Southern Italy were studied in order to evaluate the occurrence and nature of microplastics (MPs). Inland sediments were collected in the Bradano and Basento rivers (Apulo-Lucanian region, Southern Italy), while offshore sediments were collected on the continental shelf near Bari (Adriatic Sea) and Metaponto (Ionian Sea). MPs were detected and characterized using optical microscopy, micro-Fourier-Transform Infrared spectroscopy (μ-FTIR) and micro-Raman analyses. The number of MPs present varied between 144 and 1246 kg
-1 of dry sediment (468.8 ± 410,7 MPs kg-1 ) with a predominance of black fibers; no correlation emerged between MPs and sediment grain size. In river sediments, the occurrence of MPs is associated with local pollution, whereas the offshore occurrence of MPs depends on seasonal river flow and submarine canyons. Compositional analyses suggest that the main source of MPs in the studied sediments is sewage discharge from residential areas., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)- Published
- 2023
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30. A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed.
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Guagliano M, Cristiani C, Dell'Anno M, Dotelli G, Finocchio E, Lacalamita M, Mesto E, Reggi S, Rossi L, and Schingaro E
- Abstract
The controlled supply of bioactive molecules is a subject of debate in animal nutrition. The release of bioactive molecules in the target organ, in this case the intestine, results in improved feed, as well as having a lower environmental impact. However, the degradation of bioactive molecules' in transit in the gastrointestinal passage is still an unresolved issue. This paper discusses the feasibility of a simple and cost-effective procedure to bypass the degradation problem. A solid/liquid adsorption procedure was applied, and the operating parameters (pH, reaction time, and LY initial concentration) were studied. Lysozyme is used in this work as a representative bioactive molecule, while Adsorbo
® , a commercial mixture of clay minerals and zeolites which meets current feed regulations, is used as the carrier. A maximum LY loading of 32 mgLY /gAD (LY(32)-AD) was obtained, with fixing pH in the range 7.5-8, initial LY content at 37.5 mgLY /gAD , and reaction time at 30 min. A full characterisation of the hybrid organoclay highlighted that LY molecules were homogeneously spread on the carrier's surface, where the LY-carrier interaction was mainly due to charge interaction. Preliminary release tests performed on the LY(32)-AD synthesised sample showed a higher releasing capacity, raising the pH from 3 to 7. In addition, a preliminary Trolox equivalent antioxidant capacity (TEAC) assay showed an antioxidant capacity for the LY of 1.47 ± 0.18 µmol TroloxEq/g with an inhibition percentage of 33.20 ± 3.94%.- Published
- 2023
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31. External Male Genitalia in Henoch-Schönlein Syndrome: A Systematic Review.
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Montorfani-Janett VML, Montorfani GE, Lavagno C, Gualco G, Bianchetti MG, Milani GP, Lava SAG, and Cristallo Lacalamita M
- Abstract
The external genitalia are notoriously implicated in every fifth male with Henoch−Schönlein syndrome. Nonetheless, the underlying conditions are poorly categorized. To characterize the involvement of the external male genitalia in this vasculitis, we performed a systematic review of the literature. For the final analysis, we selected 85 reports published between 1972 and 2022, which reported on 114 Henoch−Schönlein cases (≤ 18 years, N = 104) with a penile (N = 18), a scrotal (N = 77), or both a penile and a scrotal (N = 19) involvement. The genital involvement mostly appeared concurrently with or after the cutaneous features of Henoch−Schönlein syndrome, while it preceded the presentation of Henoch−Schönlein syndrome in 10 cases. Patients with penile involvement (N = 37) presented with swelling (N = 26), erythema (N = 23), and purpuric rash (N = 15). Most patients were otherwise asymptomatic except for transient micturition disorders (N = 2) or priapism (N = 2). Patients with scrotal involvement (N = 96) presented with pain (N = 85), swelling (N = 79), erythema (N = 42), or scrotal purpura (N = 22). The following scrotal structures were often involved: scrotal skin (N = 83), epididymis (N = 49), and testes (N = 39). An ischemic testicular damage was noted in nine patients (four with torsion and five without). The scrotal skin involvement was mostly bilateral, while that of the epididymis and testis were mostly (p < 0.0001) unilateral (with a significant predilection for the left side). In conclusion, this analysis allows for better categorization of the involvement of external male genitalia in Henoch−Schönlein vasculitis. Scrotal involvement can result from skin inflammation, epididymitis, orchitis, or testicular ischemia.
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- 2022
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32. Posterior reversible leukoencephalopathy syndrome associated with acute postinfectious glomerulonephritis: systematic review.
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Orlando C, Milani GP, Simonetti GD, Goeggel Simonetti B, Lava SAG, Wyttenbach R, Bianchetti MG, and Cristallo Lacalamita M
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- Antihypertensive Agents therapeutic use, Female, Humans, Magnetic Resonance Imaging, Male, Neuroimaging, Glomerulonephritis complications, Glomerulonephritis drug therapy, Hypertension drug therapy, Posterior Leukoencephalopathy Syndrome etiology
- Abstract
Background: Kidney diseases are a recognized cause of posterior reversible leukoencephalopathy syndrome, usually abbreviated as PRES. The purpose of this review was to systematically address the association between acute postinfectious glomerulonephritis and PRES., Methods: We performed a systematic review of the literature on acute postinfectious glomerulonephritis associated with PRES. The principles recommended by the Economic and Social Research Council guidance on the conduct of narrative synthesis and on the Preferred Reporting Items for Systematic Reviews and Meta-analyses were used. Databases searched included Excerpta Medica, US National Library of Medicine, and Web of Science., Results: For the final analysis, we evaluated 47 reports describing 52 cases (32 males and 20 females). Fifty patients were ≤ 18 years of age. Blood pressure was classified as follows: normal-elevated (n = 3), stage 1 hypertension (n = 3), stage 2 hypertension (n = 5), and severe hypertension (n = 41). Acute kidney injury was classified as stage 1 in 32, stage 2 in 16, and stage 3 in four cases. Neuroimaging studies disclosed a classic posterior PRES pattern in 28 cases, a diffuse PRES pattern in 23 cases, and a brainstem-cerebellum PRES pattern in the remaining case. Antihypertensive drugs were prescribed in all cases and antiepileptic drugs in cases presenting with seizures. A resolution of clinical findings and neuroimaging lesions was documented in all cases with information about follow-up., Conclusions: The main factor associated with PRES in acute postinfectious glomerulonephritis is severe hypertension. Prompt clinical suspicion, rapid evaluation, and management of hypertension are crucial. A higher resolution version of the Graphical abstract is available as Supplementary information., (© 2021. The Author(s).)
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- 2022
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33. Using a natural chlorite as catalyst in chemical recycling of waste plastics: Hydrolytic depolymerization of poly-[bisphenol A carbonate] promoted by clinochlore.
- Author
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Quaranta E, Mesto E, Lacalamita M, Malitesta C, Mazzotta E, Scelsi E, and Schingaro E
- Subjects
- Benzhydryl Compounds, Carbonates, Chlorides, Hydrolysis, Phenols, Plastics, Recycling
- Abstract
The present study describes the first example of utilization of a natural clay mineral as catalyst in a process addressed to chemical valorization of poly-[bisphenol A carbonate] (PC; (1)) wastes. A natural clinochlore was investigated for the first time as the catalyst of the hydrolysis reaction of 1, a potential route to chemical recycling of wastes of this polymeric material. At 473 K, in tetrahydrofuran (THF) as the solvent, the mineral promoted effectively the depolymerization (up to 99%, after 6 h) of 1 by H
2 O and the selective (~99%) regeneration of the monomer bisphenol A (BPA, (2)). Temperature, catalyst loading, reaction time, H2 O/PC weight ratio affected markedly the productivity of the process. The role of the catalyst was also focused: the experimental data showed that the exposed brucite-like sheets of clinochlore are involved in the hydrolysis reaction and take active part in promoting the depolymerization process., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)- Published
- 2021
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34. Bone Bruise and Anterior Cruciate Ligament Tears: Presence, Distribution Pattern, and Associated Lesions in the Pediatric Population.
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Bordoni V, di Laura Frattura G, Previtali D, Tamborini S, Candrian C, Cristallo Lacalamita M, Del Grande F, and Filardo G
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- Adolescent, Cartilage, Articular injuries, Child, Cross-Sectional Studies, Female, Femur pathology, Humans, Joint Instability pathology, Magnetic Resonance Imaging methods, Male, Prevalence, Tibia pathology, Anterior Cruciate Ligament Injuries complications, Contusions epidemiology, Knee Injuries epidemiology, Knee Joint pathology
- Abstract
Background: Bone bruise characteristics after anterior cruciate ligament (ACL) injury have been correlated with the level of joint derangement in adults. However, the literature lacks information about younger patients, whose higher ligamentous laxity may lead to different lesion patterns., Purpose: To investigate the prevalence, size, location, and role of bone bruise associated with ACL rupture in the pediatric population., Study Design: Cross-sectional study; Level of evidence, 3., Methods: Knee magnetic resonance imaging scans (MRIs) of patients aged 8 to 16 years with ACL tears from 2010 to 2018 were selected from the institution database. Inclusion criteria were open or partially open physes, less than 90 days between trauma and MRI, and no history of injury or surgery. Presence, localization, and size of bone bruise were analyzed by 2 blinded researchers and scored with the Whole-Organ Magnetic Resonance Imaging Score (WORMS) bone bruise subscale. Ligamentous, cartilaginous, meniscal, and other lesions were documented., Results: Of the 78 pediatric patients selected from the database, 54 (69%) had bone bruise. The mean area of bone bruise was larger in males than in females (femur, 3.8 ± 2.8 vs 2.2 ± 1.4 cm
2 , respectively, P = .006; tibia, 2.6 ± 1.6 vs 1.5 ± 0.8 cm2 , respectively, P = .007). The subregions most affected by bone bruise were the lateral posterior tibia and the lateral central femur (in 83% and 80% of the knees affected, respectively). A low correlation was found between age and bone bruise area (biggest areas r = 0.30, P = .03, and sum of areas r = 0.27, P = .04), but no correlation was found between age and WORMS (femur, r = -0.03, P = .85; tibia, r = -0.04, P = .76). The injuries most associated with bone bruise were 23 meniscal lesions (43%), 10 lesions of other ligaments (19.0%), 2 cartilage lesions (3.7%), and 2 patellar fractures (3.7%)., Conclusion: The prevalence of bone bruises in pediatric patients with ACL tears is high, although it seems slightly lower than the prevalence documented in adults but with similar localization. The area and the distribution pattern of bone bruises are similar among different ages. The pediatric patients had a lower presence of cartilage and meniscal lesions compared with that reported in adults, which suggests a different effect of this trauma on the knee of pediatric patients.- Published
- 2019
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35. Tracheal agenesis: optimization of computed tomography diagnosis by airway ventilation.
- Author
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Cristallo Lacalamita M, Fau S, Bornand A, Vidal I, Martino A, Eperon I, Toso S, Rougemont AL, and Hanquinet S
- Subjects
- Fatal Outcome, Female, Humans, Infant, Newborn, Intubation, Intratracheal, Laryngoscopy, Male, Trachea diagnostic imaging, Constriction, Pathologic diagnostic imaging, Tomography, X-Ray Computed methods, Trachea abnormalities
- Abstract
Tracheal agenesis is a rare and often lethal congenital defect that leads to airway emergency at birth. Computed tomography (CT) is the modality of choice to evaluate anomalous tracheal anatomy. The absence of spontaneous aeration of the tracheobronchial tree in children with tracheal agenesis makes CT interpretation difficult. We describe a procedure of airway management applied in two newborns with suspected tracheal agenesis. Correct airway management was performed immediately prior to CT examination by airway ventilation, with bag-valve mask alone in one case, and attached to an endotracheal tube placed into the esophagus in the other case. The images allowed for classification of tracheal agenesis. Computed tomography with appropriate airway ventilation is fundamental for the diagnosis of tracheal agenesis.
- Published
- 2018
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36. Sofosbuvir and velpatasvir for hepatitis C virus infection in people with recent injection drug use (SIMPLIFY): an open-label, single-arm, phase 4, multicentre trial.
- Author
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Grebely J, Dalgard O, Conway B, Cunningham EB, Bruggmann P, Hajarizadeh B, Amin J, Bruneau J, Hellard M, Litwin AH, Marks P, Quiene S, Siriragavan S, Applegate TL, Swan T, Byrne J, Lacalamita M, Dunlop A, Matthews GV, Powis J, Shaw D, Thurnheer MC, Weltman M, Kronborg I, Cooper C, Feld JJ, Fraser C, Dillon JF, Read P, Gane E, and Dore GJ
- Subjects
- Administration, Oral, Adult, Antiviral Agents adverse effects, Carbamates adverse effects, Drug Administration Schedule, Drug Packaging, Female, Genotype, Hepacivirus genetics, Hepatitis C, Chronic virology, Heterocyclic Compounds, 4 or More Rings adverse effects, Humans, Male, Medication Adherence, Middle Aged, Recurrence, Risk Factors, Sofosbuvir adverse effects, Sustained Virologic Response, Antiviral Agents therapeutic use, Carbamates therapeutic use, Hepatitis C, Chronic complications, Hepatitis C, Chronic drug therapy, Heterocyclic Compounds, 4 or More Rings therapeutic use, Sofosbuvir therapeutic use, Substance Abuse, Intravenous complications
- Abstract
Background: Despite revised guidelines that no longer exclude people who inject drugs (PWID) from treatment for hepatitis C virus (HCV) infection, many clinicians are reluctant to treat recent PWID. This study aimed to evaluate the efficacy of sofosbuvir and velpatasvir therapy in people with chronic HCV infection and recent injection drug use., Methods: In this open-label, single-arm phase 4 trial (SIMPLIFY), we recruited participants with recent injection drug use (past 6 months) and chronic HCV genotype 1-6 infection from seven countries (19 sites). Participants received oral sofosbuvir (400 mg) and velpatasvir (100 mg) once daily for 12 weeks. Therapy was given in 1-week electronic blister packs to record the time and date of each dose. The primary endpoint was the proportion of patients with sustained virological response 12 weeks after completion of treatment (SVR12; defined as HCV RNA <12 IU/mL), analysed in all patients who received at least one dose. This study is registered with ClinicalTrials.gov, number NCT02336139, and follow-up is ongoing to evaluate the secondary endpoint of HCV reinfection., Findings: Between March 29, and Oct 31, 2016, we enrolled 103 participants; 29 (28%) of whom were female, nine (9%) had cirrhosis, 36 (35%) had HCV genotype 1, five (5%) had genotype 2, 60 (58%) had genotype 3, and two (2%) had genotype 4. 61 (59%) participants were receiving opioid substitution therapy during the study, 76 (74%) injected in the past month, and 27 (26%) injected at least daily in the past month. 100 (97%) of 103 participants completed treatment; two people were lost to follow-up and one person died from an overdose. There were no virological failures. 97 (94%, 95% CI 88-98) of 103 people achieved SVR12. Three participants with an end-of-treatment response did not have a SVR; two were lost to follow-up and one had reinfection. Drug use before and during treatment did not affect SVR12. Treatment-related adverse events were seen in 48 (47%) patients (one grade 3, no grade 4). Seven (7%) patients had at least one serious adverse event; only one such event (rhabdomyolysis, resolved) was possibly related to the therapy. One case of HCV reinfection was observed., Interpretation: HCV treatment should be offered to PWID, irrespective of ongoing drug use. Recent injection drug use should not be used as a reason to withhold reimbursement of HCV therapy., Funding: Gilead Sciences., (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Published
- 2018
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37. Hydrocarbons in phlogopite from Kasenyi kamafugitic rocks (SW Uganda): cross-correlated AFM, confocal microscopy and Raman imaging.
- Author
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Moro D, Valdrè G, Mesto E, Scordari F, Lacalamita M, Ventura GD, Bellatreccia F, Scirè S, and Schingaro E
- Abstract
This study presents a cross-correlated surface and near surface investigation of two phlogopite polytypes from Kasenyi kamafugitic rocks (SW Uganda) by means of advanced Atomic Force Microscopy (AFM), confocal microscopy and Raman micro-spectroscopy. AFM revealed comparable nanomorphology and electrostatic surface potential for the two mica polytypes. A widespread presence of nano-protrusions located on the mica flake surface was also observed, with an aspect ratio (maximum height/maximum width) from 0.01 to 0.09. Confocal microscopy showed these features to range from few nm to several μm in dimension, and shapes from perfectly circular to ellipsoidic and strongly elongated. Raman spectra collected across the bubbles showed an intense and convolute absorption in the range 3000-2800 cm
-1 , associated with weaker bands at 1655, 1438 and 1297 cm-1 , indicating the presence of fluid inclusions consisting of aliphatic hydrocarbons, alkanes and cycloalkanes, with minor amounts of oxygenated compounds, such as carboxylic acids. High-resolution Raman images provided evidence that these hydrocarbons are confined within the bubbles. This work represents the first direct evidence that phlogopite, a common rock-forming mineral, may be a possible reservoir for hydrocarbons.- Published
- 2017
- Full Text
- View/download PDF
38. Use of natural clays as sorbent materials for rare earth ions: Materials characterization and set up of the operative parameters.
- Author
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Iannicelli-Zubiani EM, Cristiani C, Dotelli G, Gallo Stampino P, Pelosato R, Mesto E, Schingaro E, and Lacalamita M
- Subjects
- Adsorption, Aluminum Silicates chemistry, Clay, Ions chemistry, Photoelectron Spectroscopy, Powder Diffraction, Spectrophotometry, Atomic, X-Ray Diffraction, Bentonite chemistry, Metals, Rare Earth chemistry, Waste Disposal, Fluid methods, Wastewater analysis
- Abstract
Two mineral clays of the montmorillonite group were tested as sorbents for the removal of Rare Earths (REs) from liquid solutions. Lanthanum and neodymium model solutions were used to perform uptake tests in order to: (a) verify the clays sorption capability, (b) investigate the sorption mechanisms and (c) optimize the experimental parameters, such as contact time and pH. The desorption was also studied, in order to evaluate the feasibility of REs recovery from waters. The adsorption-desorption procedure with the optimized parameters was also tested on a leaching solution obtained by dissolution of a dismantled NdFeB magnet of a hard-disk. The clays were fully characterized after REs adsorption and desorption by means of X-ray powder diffraction (XRPD) and X-ray photoelectron spectroscopy (XPS); the liquid phase was characterized via Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES) analyses. The experimental results show that both clays are able to capture and release La and Nd ions, with an ion exchange mechanism. The best total efficiency (capture ≈ 50%, release ≈ 70%) is obtained when the uptake and release processes are performed at pH=5 and pH=1 respectively; in real leached scrap solutions, the uptake is around 40% but release efficiency is strongly decreased passing from a mono-ion system to a real system (from 80% to 5%). Furthermore, a strong matrix effect is found, with the matrix largely affecting both the uptake and the release of neodymium., (Copyright © 2015 Elsevier Ltd. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
39. Erdheim-Chester disease: a systematic review.
- Author
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Cives M, Simone V, Rizzo FM, Dicuonzo F, Cristallo Lacalamita M, Ingravallo G, Silvestris F, and Dammacco F
- Subjects
- Adrenal Cortex Hormones therapeutic use, Adult, Bone and Bones pathology, Central Nervous System pathology, Erdheim-Chester Disease diagnosis, Erdheim-Chester Disease drug therapy, Erdheim-Chester Disease genetics, Humans, Kidney pathology, Male, Myocardium pathology, Point Mutation, Prognosis, Proto-Oncogene Proteins B-raf genetics, Erdheim-Chester Disease pathology
- Abstract
Erdheim-Chester disease (ECD) is a rare form of non-Langerhans-cell histiocytosis, associated in more than 50% of cases to BRAF(V600E) mutations in early multipotent myelomonocytic precursors or in tissue-resident histiocytes. It encompasses a spectrum of disorders ranging from asymptomatic bone lesions to multisystemic, life-threatening variants. We reviewed all published reports of histologically-confirmed ECD and explored clinical, radiological, prognostic and therapeutic characteristics in a population of 448 patients, including a unique patient from our Department. To find a clinically relevant signature defining differentiated prognostic profiles, the patients' disease features were compared in relation to their CNS involvement that occurred in 56% of the entire population. Diabetes insipidus, visual disturbances, pyramidal and extra-pyramidal syndromes were the most recurrent neurological signs, whereas concomitant pituitary involvement, retro-orbital masses and axial lesions in the presence of symmetric bilateral osteosclerosis of long bones depicted the typical ECD clinical picture. Patients with CNS infiltration showed a lower occurrence of heart involvement and a higher incidence of bone, skin, retro-peritoneal, lung, aortic and renal infiltration. No difference in the therapeutic algorithm was found after stratification for CNS involvement. A better understanding of the disease pathogenesis, including BRAF deregulation, in keeping with improved prognostic criteria, will provide novel suggestions for the management of ECD., (Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
40. The correct assignment of stereochemistry in di-μ-dichlorido-bis{bis[2-(5-benzylsulfonyl)-3-fluoro-2-(pyridin-2-yl)phenyl-κ2N,C1]iridium(III)} toluene monosolvate.
- Author
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Mesto E, Scordari F, Lacalamita M, De Cola L, Ragni R, and Farinola GM
- Abstract
The title complex, [Ir2(C18H13FNO2S)4Cl2]·C7H8, was crystallized from dichloromethane solution under a toluene atmosphere. It is a dimeric complex in which each of the two Ir(III) centres is octahedrally coordinated by two bridging chloride ligands and by two chelating cyclometalated 2-(4-benzylsulfonyl-2-fluorophenyl)pyridine ligands. The crystal structure analysis unequivocally establishes the trans disposition of the two cyclometalated ligands bound to each Ir(III) centre, contrary to our previous hypothesis of a cis disposition. The latter was based on the (1)H NMR spectra of a series of dimeric benzylsulfonyl-functionalized dichloride-bridged iridium complexes, including the compound described in the present work [Ragni et al. (2009). Chem. Eur. J. 15, 136-148]. The toluene solvent molecules, embedded in cavities in the crystal structure, are highly disordered and could not be modelled successfully; their contribution was removed from the refinement using the SQUEEZE routine in the program PLATON [Spek (2009). Acta Cryst. D65, 148-155].
- Published
- 2013
- Full Text
- View/download PDF
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