Magnetic properties of metal-substituted haematite

Mineral and isothermal magnetic properties of Al-, Mn- and Ni-substituted haematites were characterized and their relationships evaluated in order to interpret better the results of magnetic analyses of soils and recent sediments. Aluminium, manganese and nickel haematites generally behaved as single-domain (SD) particles. The influence of incorporated Al on the magnetic behaviour of haematite was consistent with Al acting as a paramagnetic dilutent. Mass magnetic susceptibility ( χ ) and SIRM₈₀₀ decreased as the level of Al substitution increased. Incorporation of Mn and Ni increased χ , which could be associated with enhancement of the spin canting effect of haematite. The stability of SIRM₈₀₀ to demagnetization for Al-haematite appears to be related to a defect mechanism associated with the development of smaller crystallites arising from Al substitution. Magnetic domain rotation or flipping was probably inhibited, being blocked by structural defects during magnetization and demagnetization, and resulted in a low but stable partial SIRM (SIRM₈₀₀ ). %IRM/SIRM₈₀₀ demagnetization curves and estimated ( B _o )_CR values of ≤100  mT for Mn-haematite indicate pseudo-single-domain/multidomain-like behaviour despite Mn-haematite having particle and crystallite dimensions similar to Ni-haematite, which did not show this behaviour. Data indicate that parameters involving unsaturated, partial SIRM should be used with caution in magnetic studies of soils and sediments.     

Limits to the age of the Lapstone monocline,N.S.W.—a palaeomagnetic study

The age of formation of the Lapstone Monocline has been long considered to be late Pliocene/early Pleistocene (the Kosciusko Uplift) but it is now generally thought to be much older. Palaeomagnetic data from haematite‐rich beds within the Hawkesbury Sandstone on and about the monocline indicate that it formed before the oldest haematite was introduced to these beds. The age of this oldest haematite is 15 ± 7 Ma. On the basis of these data, the age of the monocline is unlikely to be less than 8 Ma, probably exceeds 15 Ma, and could be older than 22 Ma.     

Electron Probe Microanalysis of Variable Oxidation State Oxides: Protocol and Pitfalls

Electron probe microanalysis of geological oxide materials relies on stoichiometric considerations to estimate the content of undetermined oxygen and thus calculate ZAF (atomic number, absorption, fluorescence) matrix correction factors, requiring the valences of cations in the corresponding software to be unambiguously defined. However, stoichiometric ZAF corrections may be problematic in the presence of other undetermined elements or variable valence state cations. Herein, we analyse several oxides containing such cations, that is magnetite (Fe₃O₄), haematite (Fe₂O₃), hausmannite (Mn₃O₄) and cuprite (Cu₂O). We compare data re‐calculated for incorrect valence states ( Method 1 ) with reference values, revealing incorrect results, due to an incorrect amount of oxygen used in the matrix correction. Some solid‐solution series of haematite and magnetite were also modelled in CalcZAF program to prove the relative errors when the incorrect oxygen is used. To resolve these issues, we describe two accurate methods. Method 2 uses the true valence states of analysed elements. In Method 3, all cations are analysed as metals, with the content of undetermined oxygen determined by difference. As EPMA software does not allow the use of non‐integer valences, Method 3 is applicable to cations with non‐integer or dubious valences in cases where these non‐integer valences cannot be defined.