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Fish shelf-life extension is a topic of great interest. In this study the behaviour of salted and unsalted farmed and wild European sea bass (Dicentrarchus labrax) fillets during storage was analysed through the evolution of their volatile metabolites. Farmed and wild sea bass fillets were brine-salted for 15 or 75 min, or dry-salted, vacuum-packed and stored at 4 °C for up to 1 month, and their headspaces were studied by Solid Phase Micro extraction-Gas Chromatography/Mass Spectrometry (SPME-GC/MS).; Results: At the same storage time, unsalted wild fillets contained, in general, a higher number and abundance of volatile compounds coming from microbiological or endogenous enzymatic activity than unsalted farmed ones. The more intense the salting, the lower the number and abundance of microbiological spoilage metabolites, especially in wild samples. The appearance of oxidation metabolites only in dry-salted wild samples evidences that this kind of salting provokes a certain oxidation in these samples.; Conclusions: The better performance of farmed than wild fillets suggests that salted farmed fillets, vacuum-packed and stored under refrigeration conditions, could be a successful alternative to diversify the presence of sea bass in the market. © 2016 Society of Chemical Industry.; © 2016 Society of Chemical Industry.

BACKGROUND Farmed and wild European sea bass (Dicentrarchus labrax) could be distinguished by its volatile metabolites, an issue not addressed until now. The aim of this work was to study these metabolites by solid-phase microextraction followed by gas chromatography/mass spectrometry (SPME-GC/MS). RESULTS Both farmed and wild sea bass have a great number of volatile metabolites, most of them being in low concentrations. These include alcohols, aldehydes, ketones, alkylfurans, acids, aliphatic and aromatic hydrocarbons, terpenes, sulfur and nitrogen derivatives, 2,6-di-tert-butyl-4-methylphenol and one derived compound, as well as 2,4,7,9-tetramethyl-5-decyne-4,7-diol, this latter compound presumably resulting from environmental contamination. Important differences have been detected between both types of sea bass, and also among individuals inside each group. Farmed specimens are richer in volatile metabolites than the wild counterparts; however, these latter, in general, contain a high number and abundance of metabolites resulting from microbial and enzymatic non-oxidative activity than the former. CONCLUSIONS Clear differences in the volatile metabolites of wild and farmed sea bass have been found. A great deal of valuable information on sea bass volatile metabolites has been obtained, which can be useful in understanding certain aspects of the quality and safety of raw and processed sea bass. © 2015 Society of Chemical Industry

BACKGROUND: The volatile components of virgin and refined oils whose compositions were very different in terms of oleic, linoleic and linolenic acyl groups were studied by solid phase microextraction (SPME) followed by gas chromatography/mass spectrometry (GC/MS), and their composition of acyl groups was determined by proton nuclear magnetic resonance 1H NMR. The virgin oils studied were olive, linseed and walnut oils, while the refined oils were sunflower and rapeseed oils. RESULTS: Large differences were found among the headspace compositions of the virgin oils. These were due in part to compounds that could be considered as markers of different vegetable origins and manufacturing processes, but also to compounds resulting from degradative oxidation of the main acyl group components. By virtue of their being refined, fewer components were present in the refined oils, although differences in their headspaces were found owing to the presence of compounds resulting from oxidation of the determined acyl groups. CONCLUSION: The studied oils show specific characteristics regarding not only their main components, which are well known, but also their volatile components. The latter provide information on some of the processes to which oils have been submitted, on their oxidation level, on their botanical origin and on the compounds responsible for their odour. Copyright © 2011 Society of Chemical Industry

The oxidation process of sunflower and corn oils at 70 °C with circulating air has been studied by means of 1H nuclear magnetic resonance (NMR). The changes produced in the two oils are compared not only in relation to the rate of degradation of acyl groups but also with reference to both the rate of formation and degradation of primary oxidation products as well as the rate of formation of secondary oxidation products such as aldehydes. Special attention is paid to the evolution of the different kinds of aldehydes formed throughout the process. The great ability of these oils to produce geno- and cytotoxic aldehydes under the above conditions is proved. Moreover, peroxide and anisidine values of corn oil throughout its oxidation process have also been determined and the results obtained have been compared with those provided by the 1H NMR spectra, showing good agreement. Copyright © 2005 Society of Chemical Industry

Farmed salmon fillets were dry-salted for 24 h. Both salted and unsalted samples were submitted to oxidative conditions at 50 °C in an oven with circulating air. Lipids of both samples were extracted daily from aliquots and studied by Fourier transform infrared spectroscopy. The infrared spectra of salmon lipids are similar to those of vegetable edible oils, with differences in the frequency and absorbance of some bands due to their different acyl group compositions. The infrared spectra of salted and unsalted fish lipid samples remain unchanged during a period of time, which is shorter for the salted salmon. After this period, changes in the frequency and absorbance of some bands of the spectrum are observed owing to the presence of oxidation products. Therefore the reduction in the oxidative stability of farmed salmon lipids caused by the dry-salting process is proved and the usefulness of this technique for studying the oxidative stability of fish lipid samples as well as their oxidation degree is shown. Copyright © 2004 Society of Chemical Industry

The 1H nuclear magnetic resonance (NMR) spectra of 36 edible oil samples of 15 different botanical origins were recorded with a 300 MHz instrument using deuterated chloroform as solvent. The assignment of each of their peaks was made by comparison with those of standard compounds, tristearin, triolein, trilinolein and trilinolenin. For the first time, certain spectral regions of interest, conveniently expanded, together with the chemical shifts of their peaks, are given for 15 oil samples of different botanical origin. The usefulness of each of these spectral regions in the differentiation of oils is discussed. It is shown that 1H NMR spectra can be considered as the fingerprint of each oil sample. It is proved that they provide a great deal of information which permits discrimination between oils of different composition. This discrimination can be made in many cases with the naked eye by observation of certain spectral signals, without any other additional determinations. © 2003 Society of Chemical Industry

Solid phase microextraction followed by gas chromatographylmass spectrometry of raw and smoked black bream and rainbow trout was carried out. The volatile components of the raw fish belong to a limited number of groups of compounds. Raw black bream has a higher presence of acids than raw trout, while the latter contains more alcohols, hydrocarbons, esters and phenol derivatives; both contain similar concentrations of saturated aldehydes. The volatiles of the smoked fish basically comprise the compounds also detected in the raw fish together with others produced during the processing. Smoke components detected in both smoked fish species were mainly phenol, guaiacol and syringol derivatives, ketones, acetic acid and some polycyclic aromatic hydrocarbons. Smoked black bream contained a higher number and higher concentrations of smoke components than smoked rainbow trout. Large variations in concentrations of smoke components in the smoked fish samples indicated that the smoking process had not been totally homogeneous. The presence of autoxidatively derived compounds, such as unsaturated aldehydes, was mainly detected in some smoked bream samples, showing that this degradation process is not occurring homogeneously. The usefulness of the applied techniques for the study of volatile components of raw and smoked fish is shown. Le but de cette etude est d'etablir s'il existe des differences entre les composes volatils d'especes tres differentes de poissons dans des conditions d'alimentation et d'environnement differents. Elle determine aussi dans quelle mesure le procede de fumage modifie la composition de ces composes dans chacune des especes. L'utilite des techniques de microextraction en phase solide et de chromatographie gazeuse / spectrometrie de masse pour l'evaluation des composes volatils dans ces produits est demontree.

Farmed and wild European sea bass (Dicentrarchus labrax) could be distinguished by its volatile metabolites, an issue not addressed until now. The aim of this work was to study these metabolites by solid-phase microextraction followed by gas chromatography/mass spectrometry (SPME-GC/MS).Both farmed and wild sea bass have a great number of volatile metabolites, most of them being in low concentrations. These include alcohols, aldehydes, ketones, alkylfurans, acids, aliphatic and aromatic hydrocarbons, terpenes, sulfur and nitrogen derivatives, 2,6-di-tert-butyl-4-methylphenol and one derived compound, as well as 2,4,7,9-tetramethyl-5-decyne-4,7-diol, this latter compound presumably resulting from environmental contamination. Important differences have been detected between both types of sea bass, and also among individuals inside each group. Farmed specimens are richer in volatile metabolites than the wild counterparts; however, these latter, in general, contain a high number and abundance of metabolites resulting from microbial and enzymatic non-oxidative activity than the former.Clear differences in the volatile metabolites of wild and farmed sea bass have been found. A great deal of valuable information on sea bass volatile metabolites has been obtained, which can be useful in understanding certain aspects of the quality and safety of raw and processed sea bass.

The lipids of 16 farmed and wild European sea bass (Dicentrarchus labrax) samples were studied by Fourier transform infrared (FTIR) spectroscopy. The spectroscopic parameters which would be useful when distinguishing between both fish origins were analysed.It was shown, for the first time, that the frequency and the ratio between the absorbance of certain bands are efficient and reliable authentication tools for the origin of sea bass. Furthermore, relationships between infrared data and fish lipids composition referring to the molar percentage or concentration of certain acyl groups were also studied. It was proved that some infrared spectroscopic data (the frequency of certain bands or the ratio of the absorbance of others), are very closely related to the composition of sea bass lipids. It was shown for the first time that certain infrared spectroscopic data could predict, with a certain degree of approximation, the molar percentage, or concentration, of omega-3, docosahexaenoic (DHA) and di-unsaturated omega-6 (linoleic) in sea bass lipids.The consistency of the results confirms the usefulness of FTIR spectroscopy to detect frauds regarding sea bass origin, and to provide important compositional data about sea bass lipids from the nutritional and technological point of view.

The oxidation of a broad collection of commercial edible oils, including extra virgin olive, olive, sesame, sunflower, corn, unknown seed, soybean, safflower, rapeseed, peanut and walnut oils, was monitored by Fourier transform infrared spectroscopy. Samples were kept in a convection oven with air circulating at 70 °C. Duplicate spectra were collected each day of the experiment by applying a film of pure oil between two KBr disks. The frequency and absorbance of each infrared band were automatically registered by a macro program. Ratios between absorbances of different bands of the spectra were calculated. Changes in frequency values of different bands and in ratios between absorbances of some bands allow different stages of the oxidation process to be distinguished as well as determining their oxidative stability in a simple and fast way, showing the usefulness of this technique in monitoring oil oxidation processes. © 2000 Society of Chemical Industry

The common components found in smoke flavourings are carbonyl derivatives, acids, esters and lignin monomers such as alkyl-aryl ethers and phenol derivatives. Recently the presence of lignin dimers has been noted. In addition to these compounds, lignin trimers and new lignin dimers have been detected in the brown layer left by a smoke flavouring on the wall of the receptacle in which it was contained; these compounds tend to migrate towards the wall of the container and have not been previously described as smoke or smoke flavouring components. Lignin trimers and dimers are important in the preservation of smoked foods for their known high antioxidant activity, even higher than that of the lignin monomers. The mass spectral data of a large number of lignin trimers and dimers are given and can be useful for future studies of smoke flavourings and smoked food as well as in beverage studies and for the characterisation of woods to be used in the beverage industry. © 1999 Society of Chemical Industry

An aqueous smoke flavouring from Thymus vulgaris L was obtained. The qualitative and quantitative composition of its dichloromethane extract was studied by gas chromatography and gas chromatography/mass spectrometry. In addition to the common smoke components such as aldehydes, ketones, diketones, esters, acids, furan and pyran derivatives, alkyl aryl ethers, phenol, guaiacol and syringol derivatives, some terpenic compounds were detected. Differences between this aqueous liquid smoke and others from various kinds of wood are due not only to the absence or presence of some compounds but also to the proportions of the different groups of components present in the mixture. Some aldehydes, esters, guaiacol and its derivatives and terpenic compounds contribute to the overall odour of this liquid smoke more significantly than the ketones, furan and pyran derivatives, acids, phenol and its derivatives and syringol. The yield in smoke components obtained from the pyrolysis of Thymus vulgaris L at 488 °C is of a similar order to that obtained from other woods. © 1999 Society of Chemical Industry

The use of infrared spectroscopy in the study of fats and oils is reviewed. The importance of the mid-infrared region in the study of lipids is shown. Differences between dispersive and Fourier-transform infrared techniques are commented on and the experimental methods used in the handling of oil and fat samples are reported. The assignment of oil and fat bands of mid-infrared spectra is made, and the usefulness of this technique to characterise oils and fats and to detect adulterations is reviewed. The application of spectroscopic data to determine the degree of unsaturation or iodine value, trans- double bonds content, free fatty acid content, average chain length or saponification number, solid fat content, as well as peroxide and anisidine values, is commented on. Also, the importance of this technique for monitoring oxidation processes is shown. © 1997 SCI.

Vitis vinifera L shoots and Fagus sylvatica L wood were used to obtain aqueous smoke flavouring preparations. Both flavourings have a gold colour and pleasant odour. The flavour components of both samples are extracted with dichloromethane. The identification and quantitation of the components of the extracts are carried out by means of gas chromatography/mass spectrometry, and gas chromatography with flame ionisation detection. In both preparations carbonyl derivatives are in higher concentrations than phenol derivatives. Compounds that confer sweet, burnt and pungent flavours are in higher concentrations in the Vitis vinifera L shoots smoke flavouring, and compounds that give smoky flavours are in higher concentrations in the Fagus sylvatica L wood smoke flavouring. Ratios between the concentrations of the main components are proposed as parameters in order to characterise smoke and smoke flavourings, manufactured under specific conditions, from a specific wood. Finally, the yield of some components from a fixed amount of wood is also given.

The compositions of the essential oils of Rosmarinus officinalis L, Salvia lavandulifolia V and Lavandula latifolia M, obtained by steam distillation from plants cultivated in the northeast of Spain, have been studied by gas chromatography and gas chromatography/mass spectrometry. The essential oil of rosemary appears to be more complex and richer in flavour notes than other previously studied Spanish rosemary oils, and has an intermediate ratio of α-pinene and of 1,8-cineole in relation to essential oils of rosemary of different geographical origins, but higher proportions of camphor, verbenone and linalool. The essential oil of sage has proportions of 1,8-cineole, camphor, endo-borneol, trans-caryophyllene and α-humulene closer to commercial Salvia officinalis L than to other Spanish sages of different geographical locations, and the difference from commercial Salvia officinalis L is due principally to the higher ratio of terpene hydrocarbons and the lower proportion of thujone in the Spanish sage studied here. The essential oil of the spike lavender has the same main components and similar proportions as other Spanish wild and commercial spike lavender essen-tial oils, but shows differences in the nature of the minor components (rhodinol fraction).