UNIVERSITY OF SÃO PAULO STATE
UNESP- RIO CLARO
Institute of Geosciences and Exact Sciences
Chronology and Chronometry research group
Group photo of the participants of Thermo2016 in Maresias, Brazil
Participants of the pre-conference field trip Thermo2016
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Group photo of the participants of Thermo2016 in Maresias, Brazil
NEWS
The 15th International Conference on Thermochronology was held in Maresias Brasil. Visit https://thermo2016.rc.unesp.br/
Catodoluminescence-Stereomicroscope Laboratory
The laboratory a range of digital microscopes for transmitted and reflected light microscopy, and cathodoluminescence (CL) imaging.
Zeiss Axioplan and Leica magnifying glass
Zeiss Axioplan and Leica magnifying glass for handpick and mount procedures.
Zeiss Stereo Discovery V.12
It has both transmitted (polarized) and reflected light capabilities. Prior to loading samples into Pt tube for (U-Th)/He dating, all grains are digitally photographed using a Zeiss digital camera 5.0 Mb and all digital pictures are archived.
Lumic HC3-LM cathodoluminescence microscope
In a CL microscope an electron beam is accelerated to the surface of a thin section of a solid sample (rock, mineral, ceramics, glass) in order to induce the emission of visible light (luminescence). Thus, CL microscopy allows to make visible structures within crystals or fabrics which cannot be seen at normal light conditions. For example, valuable informations on the growth of minerals can be obtained or impurities and inhomogeneities in a ceramic become visible. A cathodoluminscence microscope is a combination of an electron microscope and a light microscope. The lumic HC3-LM cathodoluminescence microscope is designed to study the luminescence characteristics of common polished thin section surfaces irritated by an electron beam. These colors can be digitally imaged to map out the often highly detailed growth history of minerals. In addition, the precise wavelengths emitted from a sample can be obtained with the spectroscopy system. This visible light spectrum allows one to more precisely identify individual components of luminescence.