http://www.sciencedirect.com/science/article/pii/S1674987111001113

The Rheic Ocean was one of the most important oceans of the Paleozoic Era.It lay between Laurentia and Gondwana from the Early Ordovician and closed to produce the vast Ouachita-Alleghanian -Variscan orogen during the assembly of Pangea.Rifting began in the Cambrian as a continuation of Neoproterozoic orogenic activity and the ocean opened in the Early Ordovician with the separation of several Neoproterozoic arc terranes from the continental margin of northern Gondwana along the line of a former suture.The rapid rate of ocean opening suggests it was driven by slab pull in the outboard lapetus Ocean.The ocean reached its greatest width with the closure of lapetus and the accretion of the periGondwanan arc terranes to Laurentia in the Silurian.Ocean closure began in the Devonian and continued through the Mississippian as Gondwana sutured to Laurussia to form Pangea.The ocean consequently plays a dominant role in the Appalachian-Ouachita orogeny of North America,in the basement geology of southern Europe,and in the Paleozoic sedimentary,structural and tectonothermal record from Middle America to the Middle East.Its closure brought the Paleozoic Era to an end.     

Reducing Sb-leaching from municipal solid waste incinerator bottom ash by addition of sorbent minerals

This paper investigates the mechanisms controlling Sb-leaching from fresh Municipal Solid Waste Incinerator (MSWI) bottom ash, as well as the possibilities of controlling the extent of Sb-leaching by the addition of sorbent minerals to the bottom ash. In alkaline MSWI bottom ash Sb is possibly incorporated in ettringite-like minerals. When weathering/carbonation continues the ettringite dissolves resulting in a mobilisation of Sb. At neutral pH values the leaching of Sb is likely to be controlled by sorption to amorphous Fe/Al-(hydr)oxides. It has been shown that Sb can effectively be removed from solution if salts of Fe(III) or Al(III) are added to the bottom ash. This addition of Fe(III)/Al(III)-salts leads to (1) the in-situ precipitation of Fe/Al-hydroxides and sorption/coprecipitation of contaminants such as Sb, and (2) a lower bottom ash pH and thus an increased affinity of oxyanions for sorption to Fe/Al-(hydr)oxides.     

A Protocol for the Determination of the Rare Earth Elements at Picomole Level in Rocks by ICP-MS: Results on Geological Reference Materials USGS PCC-1 and DTS-1

Rare earth element analyses are widely used in geology, environmental science and archaeology. Over the past decade inductively coupled plasma-mass spectrometry has become an important source of rare earth data on geological material. However, ICP-MS analysis of rock samples without pre-concentration can be problematic because of complex sample matrices that can generate significant molecular isobaric interferences on rare earth peaks and which need to be corrected. Such problems are exacerbated for ultramafic rocks because the low levels of rare earth elements demand more concentrated solutions in order to maintain signals above background levels. These high solid loads result in intra-run changes in instrument sensitivity which need to be monitored. Pre-concentration chemistries have been developed in order to avoid high solid loads but these are time-consuming and must offer quantitative recoveries or use a yield tracer. Here, we describe an alternative method for rare earth element analysis by ICP-MS, which involves no pre-concentration and is, therefore, able to deliver data rapidly. Our approach is to apply an external correction procedure, based on the analysis of a reference material closely matched in composition to the unknown samples, which allows correction for both interferences and variations in instrument sensitivity. Testing this method, we obtained accurate rare earth element results for basaltic rocks with a precision of about 2% (1s). We demonstrate that the method is also applicable to ultramafic rocks with abundances at ultra-trace (ng g⁻¹) level and present data for twelve separate dissolutions of the peridotite USGS PCC-1 and four separate dissolutions of the dunite DTS-1 reference materials. The repeatability of the data is between 3% and 9% (1s).