Illite K–Ar dating and crystal growth processes in diagenetic environments: a critical review

K–Ar dating of illitic minerals is commonly used in studies of diagenetic series applied to oil prospecting. In spite of a great number of specialized papers, some problems remain unresolved. These are mostly due to a misunderstanding of the argon accumulation process during illitization. Criteria for identifying detrital–authigenic mineral mixtures, crystal ripening, fast precipitation or continuous nucleation‐growth processes are discussed using K–Ar data available in the literature. Using different parameters, such as Δ_age (age_K–Ar ? age_strati), Δ_cryst (diagenetic age_K–Ar ? age_strati) or Δ_frac (age_{K–Arfraction} ?age_K–Arfinest), it is shown that the K–Ar age significance depends on the illite nucleation–growth processes. A ‘diagenetic age’ is obtained when these processes are rapid (the K₂O accumulation period is shorter than 2σ). If lower than this value, the K–Ar ratio depends on the proportions of new and old particles, respectively, which are controlled by the relative rates of nucleation, crystal growth and ripening.     

On the Spectral Index－Flux Density Relation for Large Samples of Radio Sources

We present new statistical results on the spectral index-flux density relation for large samples of radio sources using archival data of the most sensitive surveys, such as 6C, Miyun, WENSS, B3, NVSS, GB87. Instrumental selection effects and the completeness of the catalogs are discussed. Based on the spectral indices calculated for about 200 000 sources from the WENSS (327 MHz) and NVSS (1.4 GHz) catalogs, we obtained (1) The median spectral index increases from amed --0.9 toαmed --0.8 (Svαvα), while S327 flux densities decrease from 0.1 Jy down to 25mJy. The median spectral indices nearly show no variation within the error bars when the flux density is larger than 0.1 Jy. (2) A dependence of the fraction of ultra-steep spectrum sources (USS, -1.5 <α<-1.0), steep spectrum sources (SSS, -1.0 <α< -0.5) and flat spectrum sources (FSS, -0.5≤α≤0.0) is partly responsible for the spectral flattening. Another contribution to the spectral flattening comes from the variation of αmed of steep spectrum so     

The presence of anomalous trace element levels in present day Jamaican soils and the geochemistry of Late-Miocene or Pliocene phosphorites

High levels of Cd and Zn in Jamaican soils observed in geochemical surveys are related to the presence of phosphorites of possible Late-Miocene or Pliocene age. The trace element and REE geochemistry of the phosphorites, together with SEM studies, indicate a guano origin for the phosphorites. No specific host minerals for Cd could be identified in the fossiliferous phosphorite which is characterized by uniquely high levels of Cd, Zn, Ag, Be, U and Y. However, in the soil Cd is present in lithiophorite and a complex history of pedological development is preserved in the aluminous–goethite present in the soil. The unique guano signature is preserved in the soil despite the fact that guanos themselves have either not been observed or have been destroyed by continuing karst and soil development. The phosphorite geochemical signature can be traced in the data of a 1988 island-wide soil geochemical survey, identifying areas where the Palaeo-environment that supported bird ‘rookeries’ existed in the Late-Miocene or Pliocene.     

Iron and manganese micro-precipitates within a cretaceous biosiliceous ooze from the Arctic Ocean: possible hydrothermal source

The oldest sediment most recently recovered from the Arctic Ocean is a biosiliceous ooze nearly devoid of nonbiogenic particles and exhibiting small-scale color changes. Color variations are due to changes in iron and manganese content. These elements are probably of local hydrothermal origin, and the Mn precipitation may be bacteria-mediated. An iron silicate phase seems to form at the expense of biogenic silica. The ooze deposited slowly until a sudden sediment input, probably a volcanigenic deposit now weathered to clay minerals, induced dissolution of siliceous microfossils. This clay layer contains calcium phosphate microspheres enriched in rare earth elements.