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Largemouth bass (Micropterus salmoides) is a freshwater fish originating from the United States of America (USA). This specie was introduced in Portugal (Azores) in the end of the XIX Century. Like in the USA, largemouth bass is one of the most popular freshwater sports fish in Portugal and it is very important in regional cuisine, especially in the countryside. However, there’s a lack of information about the chemical composition of largemouth bass fillet. All eaten largemouth bass in Portugal are caught in large dams and small irrigation dams because there’s no largemouth bass aquaculture industry. The aim of this work was to evaluate the chemical composition of largemouth bass fillet collected in an irrigation reservoir (39º49’27.89’’ N; 07º26’57.92’’ W) located in the Central region of Portugal. Thirteen largemouth bass were collected (average weight 349.85g ±74.23; average length 27.22cm ±1.43; average K condition factor 1.71 ±0.14) and were frozen during seven days. The cutting carcasses and the filet chemical analyses (moisture, protein, fat and ash) took place in the laboratory. In the carcass, the average amounts of viscera, spine, head, skin and filet were, respectively, 8.52% (±1.41), 17.24% (±1.29), 23.06% (±1.85), 7.58% (±0.60) and 43.59% (±1.91). In the filet, the average amounts of moisture, protein, fat and ash were, respectively, 77.67% (±1.07), 18.46% (±0.83), 0.90% (±0.31) and 1.20% (±0.05). We concluded that largemouth bass has a good filet yield with very low fat and high level of protein contents. In fact, as far as we know, these are the first results of carcass and filet characterization of largemouth bass collected in Portugal.
Pollen collected by honey bees (bee pollen) is promoted as a health food supplement with a wide range of nutritional and health beneficial properties. While honey is an important source of proteins for the bee colony, pollen is the bees' main source for other important nutrients, such as minerals, fats, fibers, carbohydrates, and other substances. The composition of pollen is rather variable and depends on the botanical origin of the pollen. In this work we studied the mineral content of bee pollen of three botanical origins (Cistus ladanifer L., Rubus ulmifolius Schott, and Calluna vulgaris (L.) Hull) and two geographic sites in the central Portugal (Caniçal and Vale Grande). Inductively coupled plasma atomic emission spectrometry (ICP-AES) was used for the determination of cadmium, chromium, copper, iron, lead, manganese, and zinc. Prior to ICP-AES measurement, the samples were mineralized by treatment with HNO3 and H2O2 at 100 °C until complete digestion. The analyzed elements presented levels corresponding to the usual reference range [1]. The concentrations of micronutrients (Cu, Fe, Mn and Zn) presented characteristic profiles which differed between the three plant species, but where similar in the two geographic areas. The main minerals observed for R. ulmifolius and C. vulgaris were Fe and Mn, and Zn for C. ladanifer. Heavy metals (Cd, Cr and Pb) were present at low concentrations (Table 1), indicating that there were no sources of contamination. In conclusion, the determination of micronutrients in pollen could be suitable for the identification of botanical species. The investigation of element profile, in combination with modern statistical data evaluation techniques, can be a promising approach to identify the botanical source of pollen.
There are some investigations regarding the physical and chemical properties of sweet cherry (Prunus avium L.) fruits, mostly their antioxidant capacity, phenol, ascorbic acid, as well as anthocyanin contents. Only little is known about the mineral content of sweet cherries. In this work we studied the 'Sweetheart' cultivar from Cova da Beira (Portugal), as this fruit is a rich source of nutritional components. Therefore, the mineral content of 'Sweetheart' cherry was studied. Inductively coupled plasma atomic emission spectrometry (ICP-AES) was used for the determination of minor and major elements. Prior to ICP-AES measurement, the samples were mineralized with a mixture of HNO3 and H2O2. Based on obtained results the content of minor elements was (Cu) 0.107, (Fe) 0.325, (Mn) 0.204 and (Zn) 0.090 mg 100 g-1. The concentrations of major elements were (Na) 0.629, (Ca) 16.0, (Mg) 24.0, (P) 23.6 and (K) 523 mg 100 g-1. For Mg and K, 'Sweetheart' cherry presented higher concentrations than literature: (Mg) 11.0 and (K) 222 mg 100 g-1. And similar concentrations were assessed for Cu, Fe, Zn, P and Ca: (Cu) 0.060, (Fe) 0.36, (Zn) 0.070, (P) 21.0 and (Ca) 13 mg 100 g-1. The results suggested that 'Sweetheart' cherries are rich in various essential elements, with main emphasis for K and Mg, and might be considered as an important dietary mineral enrichment for individuals deficient in mineral elements.
Nowadays customers demand objective and trustworthy information about the geographical origin of agricultural products. The mineral composition of agricultural products and its relation with their terroir has been shown to be a useful tool in differentiating commodities produced in a limited region and subjected to certain quality requirements. Cereja da Cova da Beira is the legal term used to denominate cherries produced in the Cova da Beira region (PGI - protected geographical indication) at central eastern part of Portugal, since 1996. In order to establish a methodology to certify its origin, the mineral profile of 'Sweetheart' cherry stone from Cereja da Cova da Beira , was studied. Quantification of major (Ca, Mg, K, P and Na) and minor elements (Cu, Fe Mn and Zn) of stones was carried out by inductively coupled plasma atomic emission spectrometry (ICP-AES). The results showed that, among major elements, Ca was the predominant mineral (1424.62 mg kg-1, dry weight), followed by K and Mg, presenting similar concentrations (1092.17 and 987.55 mg kg-1, respectively), P (271.10 mg kg-1), and Na (24.71 mg kg-1). Regarding micro elements, Mn showed the highest mean value (19.71 mg kg-1), followed by Fe (17.59 mg kg-1), and Cu and Zn with similar levels (7.61 and 6.73 mg kg-1, respectively). On the basis of chemometric pattern recognition procedures, the mineral content of agricultural products and its relation with their area of production can be a useful tool in differentiating commodities produced in a limited region and subjected to certain quality requirements.
Largemouth bass (Micropterus salmoides) is a very important fresh water fish in the Portuguese regional cuisine mainly in the countryside (Central region and north Alentejo). Because there’s no aquaculture industry, all eaten largemouth bass in Portugal are collected in large dams (Basins of Tejo and Guadiana rivers) and small irrigation dams. For decades, the Tejo River received environmental pollutants from non-point and point sources that included intensive agriculture, industrial entities, municipalities and nuclear power plant. The aim of this work was to evaluate some metals (Cd, Cr, Cu, Fe, Hg, Mn, Pb, Zn) present on largemouth bass muscle tissue collected in the section of Tejo River that makes border between Portugal and Spain (TR) (N=9) and collected in three irrigation reservoirs (IR) located near Castelo Branco – Portugal (N=11). Individual were weighted and measured. Age was determined by examining fish scales, and sex determined by gonads observation. Samples for liver, dorsolateral muscle and tail muscle were collected from the right side of the fish. TR average weight 435.14g (±109.15), average length 278.33mm (±23.28), average K condition factor 1.98 (±0.09) and average age 3.11 years (±0,78) were similar (P>0.05) to IR average weight 410.84g (±137.71), average length 278.36mm (±31.13), average K condition factor 1.86 (±0.17) and average age 3.18 years (±0,60). Total mercury was determined in freeze-dried samples by atomic absorption spectrometry with thermal decomposition and gold amalgamation. For the other metal analysis, freeze-dried powders were mineralized with a mixture of HNO3 and H2O2, followed by ICP-OES quantification. Cd and Pb presented concentrations below LOQ (0.025 and 0.15mg.kg-1wet.weight, respectively) for all muscle samples. These values are below legal limits in EU (0.05 and 0.3mg.kg-1wet.weight, respectively). Average Hg levels are below legal limits (0.5mg.kg-1wet.weight) and muscle presented higher levels than liver. These contaminant levels indicate that are no contamination sources in the sampling sites. Cu, Cr, Fe, Mn and Zn are essential micronutrients. Their concentrations were not significantly different between dorsal and tail muscle and were higher in liver (P>0.05), with mean concentrations on muscle being, respectively: TR 0.16 (±0.07),
Glucose and fructose are the most important monosaccharides in honey, these sugars combined in various forms comprise the di- and trisaccharide fractions of floral honey. Frutose/glucose ratio can influence the flavor of honey since fructose is sweeter than glucose. Honeys with higher fructose/glucose ratios remain liquid for longer periods. Several Chromatographic methods have been used to evaluate the sugar content of honey, although the Integrated Pulsed Amperometric Detection (IPAD) only recently became to be used. In order to characterize the sugar content in honey from different botanical origins a Dionex ICS3000 ion chromatograph was used. Separation was performed in a column “CarboPacTM PA20 3x150mm”, with a precolumn “CarboPacTM PA20 3x30mm”. Electrochemical detector in Integrated Pulsed Amperometric Detection (IPAD) mode was used. The elution was performed with a gradient with two NaOH solutions (10 and 200 mM). Standard solutions of glucose, fructose and sucrose, were used to identify and quantify the individual sugar components in the honey samples. The method showed a good separation between the compounds (resolution> 3.3 and more than 9000 theoretical plates). The response was linear in the range (0.05 to 1.00 mg/L for fructose and glucose and 0.01 to 0.20 mg/L for sucrose). The detection limits were 0.014 mg/L for glucose, 0.007 mg/L for fructose and 0.003 mg/L for sucrose. Twenty six monofloral honey samples from Erica, Citrus, Lavandula and Eucalyptus were tested. 5,000 g of each honey sample was diluted to 1 mg/L and filtered with a 0.45 m polypropylene filter prior to HPLC analysis. The results show that the fructose/glucose ratios are in accordance with the different honeys analyzed and the HPLC-IPAD is a good methodology to determine the sugar content in honey, with low solvent consumption and residues.
Este trabalho apresenta os resultados preliminares sobre a avaliação de metais pesados no pólen de plantas que vegetam em locais com diferentes níveis de poluição. Foram recolhidas amostras de pólen diretamente das plantas em zonas onde havia suspeita de contaminações diversas, nomeadamente junto a estradas, em solos com alguma contaminação e num pomar. Foi também recolhido pólen apícola em zonas consideradas mais poluídas. Analisaram-se um total de 10 amostras e para cada uma delas foram determinadas as concentrações em Cádmio(Cd), Crómio(Cr), Ferro(Fe), Zinco(Zn), Manganês(Mn), Cobre(Cu) e Chumbo(Pb). As amostras de pólen foram secas a 50ºC/24 horas e ulteriormente mineralizadas com uma mistura de HNO3 e H2O2. As concentrações dos metais referidos foram determinadas por espectrometria de emissão de plasma (ICP-OES). Nas amostras recolhidas junto a uma estrada, num pomar e num terreno perto de uma antiga lixeira verificaram-se níveis elevados de Fe, Mn e Pb enquanto que para os restantes metais analisados os níveis estavam dentro dos valores de referência para o pólen. Estes resultados preliminares fazem parte de um estudo mais completo onde se pretende correlacionar os níveis de metais pesados no pólen com os contaminantes presentes nos solos, e para já foi possível verificar que pode ser assim contaminado por eles dependendo do meio onde vegetam as plantas, confirmando a hipótese de pode ser usado como marcador ambiental.
Composição em proteína, gordura e ácidos gordos de filetes de achigãs (Micropterus salmoides Lacépède, 1802) submetidos a três regimes alimentares diferentes.
A Fourier transform infrared spectroscopic method with attenuated total reflectance (FTIR-ATR) and partial least squares (PLS) regression model for the prediction of sugar content in honey samples was calculated. Standards of trehalose, glucose, fructose, sucrose, melezitose, turanose and maltose were used to identify and quantify the individual sugar components in 63 honey samples by HPAEC-IPAD. Fructose and glucose are the highest sugars in honey with an average value of 36% and 26%, respectively. The 1stDer spectra with MSC or SLS in the wave number range from 1500 to 750cm(-1) provide the best calibration model with a r(2) of 86.60 and 86.01 with RPD of 2.6 and 2.55, respectively for fructose and glucose. For turanose and melezitose good models were also found. The FTIR-ATR showed to be a good methodology to quantify the main sugar content in honey and easily adapted to routine analysis.
Cherry is used for several processed products, resulting in a large volume of subproducts, mainly stones and peel. For evaluation of nutritional potential of some sub products, total phenol content (Folin-Ciocalteu reagent method), antioxidant activity (DPPH method), and calcium, magnesium, sodium, potassium and phosphorus content (ICP-AES) were determined in 'Sweetheart' cherry peel. Results were compared with those of 'Tulameen' raspberry fruit cultivated in the same region. Raspberry is recognised to having a high level of antioxidants, minerals and fibre. Average concentrations of 2793.8 mg gallic acid equivalent kg-1, 3450.9 mg TE kg-1, (Ca) 317.7, (Mg) 267.5, (Na) 9.8, (K) 2196.2, and (P) 407.5 mg kg-1 were found in 'Sweetheart' cherry peel. Regarding raspberries, concentrations of 1411.8 mg gallic acid equivalent kg-1, 2709.5 mg TE kg-1, (Ca) 281.9, (Mg) 227.2, (Na) 1.3, (K) 1646.7, and (P) 76.7 mg kg-1 were found. All nutritional concentrations in peel were significantly higher than in the remaining fruit, showing its potential for nutrition complement production.
Dehydration of peach is an alternative to enhance storage stability, mínimize packaging requirement and reducing post-harvest cost without a sensorial and nutritional quality loss. Preservation of fruits through sun drying techniques is practiced in Cova da Beira (a Portuguese region that has a protected geographical indication for peach), as a homemade process without quality and safety control. The aim of this work was to prepare quality dehydrated products based on a convective drying process with low cost. This process has short drying time and controlled temperature that causes minimal damage to the product without added preservatives or sugar. The samples of ‘Baby Gold’ cultivar (Prunus persica) obtained from local producer were peeled, laminated and immediately dehydrated. Samples were stored in sealed plastic containers at 25°C for subsequent analysis. In the drying process were controlled forced convection air velocity of 1.25 to 1.50 m/s, air temperature between 45 and 75°C and drying time between 7 to 11 hours. During dehydration process temperature and fruit moisture were controlled. pH, acidity, soluble solids content (SSC) and mesophilic aerobic count were performed in fresh and dehydrated fruit. Dehydrated peach were similar to homemade products. Moisture was below 12%, without significant variation of SSC and acidity (on a dry basis). No deleterious effect occurred on peach mesophilic aerobic count, since a slight decrease was registered between fresh and dehydrated fruit.
Propolis is a resinous product made by honeybees from plant-derived materials, with high content ofpolyphenols associated to several beneficial bioactivities with potential use as a natural food additive forpreservation and as a functional food ingredient. A Portuguese propolis ethanol extract (C.EE) protectedSaccharomyces cerevisiaecells from loss of viability upon exposure to H2O2, both in co- and in pre-incubation experiments. Results obtained with the comet assay suggest that lower concentrations areantigenotoxic while at higher concentrations a genotoxic effect prevails, which correlates with thecytotoxicity of high concentrations of C.EE. Flow cytometry analysis with dichlorofluorescein indicatesthat C.EE induced intracellular antioxidant activityin vivo. Overall the results suggest that C.EE isantigenotoxic but is also toxic at higher concentrations. This dual effect could be explained by thepresence of compounds known to interfere with DNA synthesis and/or cell proliferation, such as caffeicacid phenethyl ester (CAPE) and chrysin, together with antioxidants, like kaempferol, pinobanksin andpinocembrin.
The development of sensors to measure fruit internal quality variables is one of the challenges of post-harvest technology. Visible-near infrared spectroscopy (Vis/NIRS) has been a promise technique for nondestructive fruit quality assessment. This study was focused to evaluate the use of Vis/NIRS in measuring the quality parameters of intact mandarin orange fruit (Citrus clementina). The parameters studied were: firmness, color (CIEL*a*b*), peel thickness, soluble solids content (SSC), pH and total acidity (TA). A total of 120 mandarin fruit with different maturation were sampled. Reflectance NIR spectra were collected in four points of each fruit and the fruits were posteriorly analyzed for the physico-chemical parameters. Prediction models were selected based on the highest r2, lowest standard error of calibration (RMSEC) and lower number of factors used in the calculation. For color parameters (L*, a*, and b*) model had a mean square error of calibration (RMSEC) of 0.877, 1.780 and 1.589 and coefficient determination (r2) of 0.923, 0.963 and 0.852, respectively. The proposed model for the SSC had a RMSEC of 0.314 and r2 of 0.749. The results indicate that Vis/NIRS technique could provide an accurate, reliable and nondestructive method for assessing the internal quality indices.
The cherry fruit is considered a nutrient dense food with a relatively low caloric content and a significant amount of important nutrients and bioactive food components. Nowadays there are some investigations regarding on nutritional and antioxidant properties of cherries. The objective of this study was to determine the stages of maturation of Sweetheart cherry from Cova da Beira (Portugal). Physicochemical parameters: firmness, color (L*, a* and b*), soluble solids content (SSC), pH, titratable acidity (TA), total phenolic content (Folin-Ciocalteu reagent method) and antioxidant activity (DPPH method) of ‘Sweetheart’ cherry were evaluated. Three maturation stages were identified and results demonstrated that solid soluble content, phenolic compounds and antioxidant activity increase with ripening stages. For soluble solids content and total phenolic content cherries showed the following average values: 19.9, 20.5 and 22.0 º Brix and 591, 788 and 810 mg galic acid kg-1, respectively. We can consider that this cultivar has an interest in nutritional terms, which may contribute to the enhancement of 'Sweetheart' cherry from the Cova da Beira region. Additionally, these data provide complementary information which can be used to ensure the quality of this regional product, ‘Cereja da Cova da Beira’.