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1.
Spectrochim Acta A Mol Biomol Spectrosc ; 135: 203-10, 2015 Jan 25.
Article in English | MEDLINE | ID: mdl-25064504

ABSTRACT

Mine drainages of La Poderosa (El Campillo, Huelva, Spain), located in the Rio Tinto Basin (Iberian Pyrite Belt) generate carotenoid complexes mixed with copper sulfates presenting good natural models for the production of carotenoids from microorganisms. The environmental conditions of Rio Tinto Basin include important environmental stresses to force the microorganisms to accumulate carotenoids. Here we show as carotenoid compounds in sediments can be analyzed directly in the solid state by Raman and Luminescence spectroscopy techniques to identify solid carotenoid, avoiding dissolution and pre-concentration treatments, since the hydrous copper-salted paragenesis do not mask the Raman emission of carotenoids. Raman spectra recorded from one of these specimens' exhibit major features at approximately 1006, 1154, and 1520 cm(-1). The bands at 1520 cm(-1) and 1154 cm(-1) can be assigned to in-phase C=C (γ(-1)) and C-C stretching (γ(-2)) vibrations of the polyene chain in carotenoids. The in-plane rocking deformations of CH3 groups linked to this chain coupled with C-C bonds are observed in the 1006 cm(-1) region. X-irradiation pretreatments enhance the cathodoluminescence spectra emission of carotenoids enough to distinguish organic compounds including hydroxyl and carboxyl groups. Carotenoids in copper-sulfates could be used as biomarkers and useful proxies for understanding remote mineral formations as well as for terrestrial environmental investigations related to mine drainage contamination including biological activity and photo-oxidation processes.


Subject(s)
Carotenoids/chemistry , Copper/chemistry , Geologic Sediments/chemistry , Iron/chemistry , Mining , Rivers/chemistry , Spectrum Analysis, Raman , Sulfides/chemistry , Differential Thermal Analysis , Electrodes , Luminescence , Microscopy, Electron, Scanning , Spain , Spectrometry, X-Ray Emission , Thermogravimetry , X-Ray Diffraction
2.
ScientificWorldJournal ; 11: 186-98, 2011 Jan 18.
Article in English | MEDLINE | ID: mdl-21258761

ABSTRACT

Arthropod eyes are built of repeating units named ommatidia. Each single ommatidium unit contains a cluster of photoreceptor cells surrounded by support cells and pigment cells. The insect Copium eye ommatidia include additional calcium-phosphate deposits, not described in insects to date, which can be examined today using a combined set of modern microscopy and spectroscopy techniques. Teucrium gnaphalodes L'Her plants, growing in central Spain, develop galls induced by Copium insects. A survey of C. teucrii adult specimens resulted in surprising environmental scanning electron microscopy (ESEM) images, showing that their bright red eyes contain a calcium-phosphate mineralization. A complete survey of Copium eye specimens was performed by ESEM using energy-dispersive spectroscopy, backscattered electron detector and cathodoluminescence (CL) probes, field emission scanning electron microscopy, micro-Raman spectroscopy, and confocal laser scanning microscopy in order to learn ommatidia features, such as chemical composition, molecular structure, cell membrane, and internal ommatidium eye fluids and calcium-phosphate distribution deposits. The CL panchromatic images distinguish between the calcium-phosphate ommatidium and calcium-phosphate setae, which are more apatite rich. They show Raman bands attributable to bone tissue apatite biomaterials, such as bone, collagen, lipids, and blood, i.e., peptides, amide-S, amide-II, amide-III, and cytochrome P-450 scc. The chemical composition of both galls and leaves of T. gnaphalodes was determined by gas chromatography-mass spectrometry (GC-MS) of their extracts. The spectrometric and microscopic images reveal that the calcium-phosphate mineralization is formed and constrained to Copium ommatidia, which are both matrix vesicles generating mixtures of apatite collagen and operational compound eyes of the insect.


Subject(s)
Calcium Phosphates/metabolism , Eye/metabolism , Hemiptera/metabolism , Osteogenesis/physiology , Secretory Vesicles/metabolism , Animals , Eye/ultrastructure , Gas Chromatography-Mass Spectrometry , Hemiptera/ultrastructure , Microscopy, Electron, Scanning , Secretory Vesicles/ultrastructure , Spectrum Analysis, Raman
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