Sequential dehydration of the phosphate–sulfate association from Gura Dobrogei Cave, Dobrogea, Romania

A rich association of primary guano minerals, including taranakite, hydroxylapatite, brushite and gypsum with relicts of illite, kaolinite, alpha (low) quartz and calcite, was identified in the fossil bat guano deposit from Gura Dobrogei Cave, Dobrogea County, Romania. Gypsum and Ca phosphates developed preferentially on the carbonate bedrock or on fallen carbonate blocks in the guano mass, whereas taranakite was identified in the clay-rich, detritic sequences. The mineral species from the cave were characterized by optical methods, scanning electron microscopy, X-ray powder diffraction, Fourier-transform infrared and inductively coupled plasma–atomic emission spectrometry analysis. Chemically induced local dehydration of primary minerals, characterized by low temperatures (up to 100 C or even lower) and critically depending on exothermal reactions in the guano mass, prompted the formation of a secondary association, consisting of francoanellite, bassanite and monetite. Topotactic substitutions were observed in the cases of francoanellite on taranakite, bassanite on gypsum and monetite on brushite. In its turn, ardealite was partially replaced by monetite and bassanite. The sequential dehydration process seems driven by the degradation of organic matter by microbial action and also, presumably, by other exothermic reactions at local scale (e.g., oxidation of ammonia, allogenic pyrite or other organic compounds).

[1]  J. Bigot,et al.  Guano-related phosphate-rich minerals in European caves , 2019, International Journal of Speleology.

[2]  L. Lemée,et al.  Mineralogical and organic study of bat and chough guano: implications for guano identification in ancient context , 2018 .

[3]  D. Dumitraș,et al.  A re-investigation of ardealite from the type locality, the “dry” Cioclovina Cave (Şureanu Mountains, Romania) , 2017 .

[4]  T. Tămaş,et al.  Mineralogical data on bat guano deposits from three Romanian caves , 2013 .

[5]  J. García‐Ruiz,et al.  The Role and Implications of Bassanite as a Stable Precursor Phase to Gypsum Precipitation , 2012, Science.

[6]  S. Palmer,et al.  Thermal stability of the 'cave' mineral brushite CaHPO4·2H2O: Mechanism of formation and decomposition , 2011 .

[7]  P. Forti,et al.  Minerogenetic mechanisms occurring in the cave environment: an overview , 2011 .

[8]  A. Došen,et al.  Thermal decomposition of brushite, CaHPO4·2H2O to monetite CaHPO4 and the formation of an amorphous phase , 2011 .

[9]  W. L. Jorgensen,et al.  Why urea eliminates ammonia rather than hydrolyzes in aqueous solution. , 2007, The journal of physical chemistry. B.

[10]  D. Simpson,et al.  THE NATURE OF ALKALI CARBONATE APATITES Dar-B R. Stlresox, Department of Geology, Lehigh Llnitersity, , 2007 .

[11]  F. Hatert,et al.  Gypsum and bassanite in the bat guano deposit from the « dry » Cioclovina cave (Sureanu Mountains, Romania) , 2004 .

[12]  G. Stoops,et al.  Circumgranular bassanite in a gypsum crust from eastern Algeria – a potential palaeosurface indicator , 2003 .

[13]  B. Onac,et al.  Sequence of secondary phosphates deposition in a karst environment: evidence from Măgurici Cave (Romania) , 2003 .

[14]  Ştefan Marincea,et al.  The occurrence of taranakite in the "dry" Cioclovina Cave (Sureanu Mountains, Romania) , 2003 .

[15]  Matthias Epple,et al.  Die biologische und medizinische Bedeutung von Calciumphosphaten , 2002 .

[16]  P. Forti Biogenic speleothems: an overview , 2001 .

[17]  S. Weiner,et al.  Diagenesis in Prehistoric Caves: the Use of Minerals that Form In Situ to Assess the Completeness of the Archaeological Record , 2000 .

[18]  P. Anderson,et al.  Preparation and characterisation of monoclinic hydroxyapatite and its precipitated carbonate apatite intermediate. , 2000, Biomaterials.

[19]  R. Angel,et al.  Compressibility and thermal expansivity of synthetic apatites, Ca 5 (PO 4 ) 3 X with X = OH, F and Cl , 1999 .

[20]  T. Zeiske,et al.  Taranakite — the mineral with the longest crystallographic axis , 1998 .

[21]  B. Heywood,et al.  Formation of Brushite, Monetite and Whitlockite during Equilibration of Human Enamel with Acid Solutions at 37°C , 1997 .

[22]  M. Gazzano,et al.  Rietveld structure refinements of calcium hydroxylapatite containing magnesium , 1996 .

[23]  F. Abbona,et al.  Crystal habit and growth conditions of brushite, CaHPO4 ⋅ 2H2O , 1993 .

[24]  A. W. Frazier,et al.  Crystallographic properties of fertilizer compounds , 1991 .

[25]  P. Benoit Adaptation to microcomputer of the Appleman-Evans program for indexing and least-squares refinement of powder-diffraction data for unit-cell dimensions , 1987 .

[26]  J. Mandarino,et al.  The Gladstone-Dale relationship; Part IV, The compatibility concept and its application , 1981 .

[27]  C. Pak Potential etiologic role of brushite in the formation of calcium (renal) stones , 1981 .

[28]  M. Catti,et al.  Low‐temperature ordering of hydrogen atoms in CaHPO4 (monetite): X‐ray and neutron diffraction study at 145 K , 1980 .

[29]  H. Nagata,et al.  The crystal structure of synthetic calcium phosphate-sulfate hydrate, Ca<2) HPO<4) SO<4) .4H<2) O, and its relation to brushite and gypsum , 1978 .

[30]  J. A. Mandarino The Gladstone-Dale relationship; Part I, Derivation of new constants , 1976 .

[31]  Carol A. Hill,et al.  Cave Minerals of the World , 1976 .

[32]  T. Sudo,et al.  Taranakite from the onino-iwaya limestone cave at hiroshima prefecture, Japan: A new occurrence , 1975 .

[33]  S. Ross Phosphates and other Oxy-anions of Group V , 1974 .

[34]  D. W. Jones,et al.  Crystal structure of brushite, calcium hydrogen orthophosphate dihydrate: a neutron-diffraction investigation , 1971 .

[35]  B. D. Mitchell,et al.  Infra‐red, X‐ray and thermal analysis of some aluminium and ferric phosphates , 1963 .

[36]  C. Beevers,et al.  The crystal structure of dicalcium phosphate, CaHPO4 , 1955 .