Fourier transform infrared spectroscopy and chemometric analysis of white wine polysaccharide extracts

Monovarietal white wines from Maria Gomes and Bical Portuguese Bairrada varieties were prepared according to different maceration and pectic enzyme clarification procedures. The polysaccharide-rich extracts, obtained by wine concentration, dialysis, and lyophilization, were fractionated by graded ethanol precipitation. A wide range of fractions rich in polysaccharides were obtained. Using the spectral region between 1200 and 800 cm(-)(1) of the FTIR spectra of the wine polysaccharide dry extracts, using PCA and CCA chemometric methods, it was possible to discriminate the extracts on the basis of their polysaccharide composition. Moreover, it was possible to identify the wine-making processes involved and their influence on the wine polysaccharides. Furthermore, a calibration model using a PLS1 was proposed for the quantification of mannose in the samples obtained by precipitation with 60% ethanol aqueous solutions. This information will allow an expeditious assessment and monitoring of the polysaccharide composition and modifications that occur during the wine-making processing and evolution.     

Headspace solid phase microextraction (SPME) analysis of flavor compounds in wines. Effect of the matrix volatile composition in the relative response factors in a wine model.

The application of headspace solid phase microextraction (SPME) for flavor analysis has been studied. Headspace SPME sampling was tested for nine common wine flavor compounds in 10% (v/v) aqueous ethanol: linalool, nerol, geraniol, 3-methyl-1-butanol, hexanol, 2-phenylethanol, ethyl hexanoate, ethyl octanoate, and ethyl decanoate. The chemical groups (monoterpenoids, aliphatic and aromatic alcohols, and esters) showed specific behavior in SPME analysis. SPME sampling parameters were optimized for these components. Relative response factors (RRFs), which establish the relationship between the concentration of the compound in the matrix liquid solution and the GC peak area, were estimated for all compounds. Log(10)(RRF) varied from 0 (3-methyl-1-butanol) to 3 (ethyl decanoate), according to their molecular weight. Quantification by SPME was shown to be highly dependent on the matrix composition; the compounds with higher RRF were the less affected. As a consequence, the data obtained with this methodology should be used taking into consideration these limitations, as shown in the analysis of four monovarietal Bairrada white wines (Arinto, Bical, Cerceal, and Maria Gomes).     

Effect of some viticultural parameters on the grape carotenoid profile

The effect of some viticultural parameters on the grape carotenoid profile was investigated. Grape cultivar, ripeness stage, sunlight and shade exposure, altitude, and vegetative height were studied. Differences between cultivars were observed in eight different black grape varieties: Touriga Brasileira (TBR), Tinta Barroca (TB), Tinta Amarela (TA), Souz?o (S), Touriga Franca (TF), Touriga Nacional (TN), Tinta Roriz (TR), and Tinto C?o (TC), from the Douro region. TA and TBR clearly produced higher concentrations of carotenoids. Results showed that carotenoid content decreased during ripening. Decreases of lutein were observed until 66%, whereas beta-carotene slowly decreased, having a constant level until the harvest date. Carotenoid contents were consistently higher in grapes exposed to shade than in those exposed to direct sunlight in both studied white grape varieties, Maria Gomes (MG) and Loureiro (L). In the Douro Valley, high-elevation terraces, which presented a lower temperature and higher humidity during the maturation period, appeared to produce grapes with higher carotenoid values. Grapes grown with higher vegetative height seem to have higher carotenoid levels; furthermore, grapes grown with lower vegetative height had higher weight and sugar concentrations.     

中国四个地区代表性沙棘果实综合品质评价

为明确中国代表性产区沙棘品质的差异，该研究以山西、河北、内蒙古、新疆地区加工使用频率高的4个沙棘品种（中国沙棘Hippophae rhamnoides.L.Zhongguoshaji、宇璐沙棘Hippophae rhamnoides.L.Yulushaji、中国沙棘Hippophae rhamnoides.L.Zhongguoshaji、阿勒泰大果沙棘 Hippophae rhamnoides.L.Aletaidaguoshaji）为研究对象，从色泽、质地、滋味、风味、营养功能组分等方面研究其品质，测定沙棘浆中的香气成分和小分子活性物质组成，明确4个地区沙棘的综合品质，并探究不同地区沙棘综合品质的差异。结果显示：新疆阿勒泰大果沙棘色泽最鲜艳；内蒙古中国沙棘的糖酸比（1.997）最大；河北宇璐沙棘总酚含量（1.14 mg/g）最高；新疆沙棘类胡萝卜素含量（37.15 mg/100 g）最高；4种沙棘维生素C的含量无明显差异（P>0.05），约为21～23 mg/100 g；4种沙棘抗氧化活性水平存在显著差异，山西沙棘DPPH自由基清除率最高（P<0.05），内蒙古沙棘的ABTS自由基清除率和铁离子还原能力（FRAP）均最高（P<0.05）。4个地区沙棘挥发性成分差异显著（P<0.05），其中河北、内蒙古、新疆、山西沙棘中特征挥发物质分别为3-辛酮、2-庚烯醛等，异戊酸异丙酯、2-甲基丁酸丙酯等，正辛烷、2,3-二氢-2,2,6-三甲基苯甲醛，己酸戊酯、癸酸乙酯。4个地区沙棘主要多酚类物质包括奎宁酸、异鼠李素、阿洛酮糖等。4个地区沙棘14项品质指标进行因子分析，共提取3个公因子，累计方差贡献率达到100%。综合品质评价模型得出，4个地区代表性沙棘品种综合品质得分依次为河北沙棘，山西沙棘，内蒙古沙棘，新疆沙棘。该研究将为沙棘系列产品的开发原料选择提供理论依据和基础。     

不同品种和生长期嘉宝果叶片酚类及挥发性物质研究

为研究不同品种和生长期嘉宝果叶片酚类及挥发性物质的含量和组成,分别通过比色法、水蒸气蒸馏法和顶空-气相色谱/质谱联用技术,对沙巴、四季早生、福冈等9个品种嘉宝果老/嫩叶的总酚、总黄酮、精油含量和挥发性成分进行测定。结果表明,沙巴嫩叶的总酚含量(31.87%)最高;阿根廷嫩叶总黄酮含量(24.81%)最高;沙巴老叶精油含量(2.78‰)最高,其次为沙巴嫩叶(2.42‰)。老叶中相对含量在0.05%以上的挥发性化合物有31~44种,均以萜类为主;嫩叶中相对含量在0.05%以上的化合物有28~40种,同样以萜类为主。除沙巴、阿根廷、大红钻老/嫩叶和福冈老叶外,其余老/嫩叶均以倍半萜为优势成分。沙巴老叶主要成分为α-蒎烯、桉叶油醇;沙巴嫩叶为β-蒎烯和α-蒎烯;阿根廷老/嫩叶、大红钻嫩叶和白艾斯老叶为β-蒎烯;福冈老/嫩叶为β-石竹烯;四季早生、大巨红晶、艾斯卡老/嫩叶为β-胡椒烯;乔尼尔老/嫩叶为β-石竹烯、β-胡椒烯。主成分分析结果表明,单萜含氧衍生物、α-蒎烯、单萜烯、β-蒎烯、α-芹子烯是导致不同品种间嘉宝果老叶香气差异的主要物质;倍半萜烯、单萜烯、β-蒎烯、α-蒎烯、β-石竹烯是导致不同品种间嘉宝果嫩叶香气差异的主要物质。综上,沙巴嫩叶总酚含量最高,精油含量较高,活性挥发性物质蒎烯(α-蒎烯+β-蒎烯)相对含量高达62.41%,在抗菌、抗炎、抗氧化、抗肿瘤等方面有潜在的利用价值,在医药领域有极大的研究价值和开发潜力。     

Analysis of volatile compounds from various types of barley cultivars

We identified volatile compounds of barley flour and determined the variation in volatile compound profiles among different types and varieties of barley. Volatile compounds of 12 barley and two wheat cultivars were analyzed using solid phase microextraction (SPME) and gas chromatography. Twenty-six volatiles comprising aldehydes, ketones, alcohols, and a furan were identified in barley. 1-Octen-3-ol, 3-methylbutanal, 2-methylbutanal, hexanal, 2-hexenal, 2-heptenal, 2-nonenal, and decanal were identified as key odorants in barley as their concentration exceeded their odor detection threshold in water. Hexanal (46-1269 microg/L) and 1-pentanol (798-1811 microg/L) were the major volatile compounds in barley cultivars. In wheat, 1-pentanol (723-748 microg/L) was a major volatile. Hulled barley had higher total volatile, aldehyde, ketone, alcohol, and furan contents than hulless barley, highlighting the importance of the husk in barley grain aroma. The proanthocyanidin-free varieties generally showed higher total volatile and aldehyde contents than wild-type varieties, potentially due to decreased antioxidant activity by the absence of proanthocyanidins.     

Analysis of volatile compounds and triglycerides of seed oils extracted from different poppy varieties (Papaver somniferum L.)

Poppy seed oil (Oleum Papaveris Seminis) is used for culinary and pharmaceutical purposes, as well as for making soaps, paints, and varnishes. Astonishingly, hardly anything was yet known about the volatile compounds of this promising comestible. Likewise, there are no current published data about the triglyceride (TAG) composition of poppy seed oils available. In this investigation solid-phase microextraction (SPME) with DVB/Carboxen/PDMS Stable-Flex fiber was applied to the study of volatile compounds of several seed oil samples from Papaver somniferum L. (Papaveraceae). 1-Pentanol (3.3-4.9%), 1-hexanal (10.9-30.9%), 1-hexanol (5.3-33.7%), 2-pentylfuran (7.2-10.0%), and caproic acid (2.9-11.5%) could be identified as the main volatile compounds in all examined poppy seed oil samples. Furthermore, the TAG composition of these oils was analyzed by MALDI-ReTOF- and ESI-IT-MS/MS. The predominant TAG components were found to be composed of linoleic, oleic, and palmitic acid, comprising approximately 70% of the oils. TAG patterns of the different poppy varieties were found to be very homogeneous, showing also no significant differences in terms of the applied pressing method of the plant seeds.     

Application of a headspace sorptive extraction method for the analysis of volatile components in South African wines

A headspace sorptive extraction (HSSE) in combination with thermal desorption gas chromatography-mass spectrometry (TD-GC-MS) method for the analysis of volatile components (alcohols, esters, carbonyls, acids, phenols and lactones) in wine samples was developed. Extraction conditions such as salting-out effects, sorption time, stirring speed, phase ratio, extraction temperature, and effect of pH were thoroughly evaluated as part of method validation. The method was very sensitive with LODs and LOQs between 50 pg/L to 299 microg/L and 0.2 ng/L to 0.996 microg/L, respectively. Repeatability for all the compounds was between 3 and 22%. The intermediate repeatability was obtained within the acceptable range. Out of 39 volatile compounds selected, 37 were detected and quantitated. The method was found to be simple, cost-effective, sensitive, and use a small sample volume. The method was successfully applied for the routine analysis of 79 young red and white wine samples from various South African districts.     

不同干燥方式对中国对虾风味组分的影响

为了研究不同干燥方式对中国对虾风味组分的影响,该文采用热风(温度:(50±2)℃,风速:1.5 m/s,时间:8 h)、冷风(温度:18~20℃,风速:1.5 m/s,时间:56 h)、微波真空(功率500 W,真空度70 kPa,时间:40 min)、微波真空-冷风联合(先温度为18~20℃,时间27h的冷风干燥,后功率500 W,真空度70 kPa,时间10 min的微波真空干燥)4种干燥方式对其干制品的游离氨基酸组成、呈味核苷酸、等鲜量以及挥发性成分进行研究。结果表明,热风干燥后的中国对虾总游离氨基酸质量分数为63.31 mg/g,相对于对照组鲜虾(72.04 mg/g)有明显损失(P0.05);呈味核苷酸质量分数为7.9 mg/g,较对照组(9.05 mg/g)损失严重(P0.05);其等鲜量(127 g/(100 g))较鲜虾(180 g/(100 g))显著降低(P0.05);对虾产生以烤肉香味和海鲜风味为主的挥发性成分。冷风干燥使中国对虾总游离氨基酸质量分数较对照组损失偏大,其值为63.70 mg/g(P0.05);等鲜量(155(g/100 g))损失较大(P0.05);挥发性成分以烃类化合物为主,风味较寡淡。微波真空干燥后的中国对虾呈味核苷酸和等鲜量分别为9.17 mg/g和176 g/(100 g),总游离氨基酸质量分数较对照组损失较严重,为55.81 mg/g(P0.05);挥发性成分以肉香味和烤香味为主。微波真空-冷风联合干燥后的中国对虾呈味核苷酸含量最高,其值是9.90 mg/g;等鲜量值为189 g/(100 g),相对于鲜虾有所提高(P0.05);总游离氨基酸质量分数为62.84 mg/g呈现降低(P0.05);产生以烤肉香味和海鲜风味为主的挥发性成分。因此,微波真空-冷风联合干燥方式对中国对虾风味变化影响最小,是一种具有发展前景的干燥方式。     

基于GC-IMS技术的福建白茶产地判别

为了实现福建省白茶产地的快速鉴别,采用气相色谱-离子迁移谱(Gas Chromatography-Ion Mobility Spectrometry,GC-IMS)技术对福建不同产地白茶挥发性物质进行检测,结合化学计量学方法建立白茶产地判别模型。结果表明,福鼎、福安、政和、建阳和松溪各产地间白茶挥发性物质含量存在差异,政和、建阳和松溪3地制成的白茶样品相似度相对较高。GC-IMS谱图数据和241种标记物质数据均可用于白茶产地区分。GC-IMS谱图数据建立的K近邻线性判别分析(K-near Neighbor Linear Discriminant Analysis,LDA-KNN)、多层感知机线性判别分析(Multi-layer Perceptron Linear Discriminant Analysis,LDA-MLP)和支持向量机线性判别分析(Support Vector Machine Linear Discriminant Analysis,LDA-SVM)模型判别率分别为91.84%、93.88%和93.88%;标记物质建立的Adaboost线性判别分析(LDA-Adaboost)、决策树线性判别分析(LDA-DecisonTree)、LDA-KNN、LDA-MLP、随机森林线性判别分析(LDA-Random Forest)和LDA-SVM模型判别率均为100%。结果表明基于标记物质数据建立的6种模型能更有效对白茶产地进行区分。研究结果为福建白茶原产地保护提供技术支持。     

Comparison of volatile concentrations in hand-squeezed juices of four different lemon varieties

Fresh juices of four Italian cultivars of lemons (Citrus limon Burm) have been analyzed by headspace solid phase microextraction coupled to gas chromatography and gas chromatography-mass spectrometry (GC-MS). The best results have been obtained with the 2 cm 50/30 microm divinylbenzene/carboxen on poly(dimethylsiloxane) fiber, using a homogenization time of 1 h at 40 degrees C and a sampling period of 30 min. A total of 35 volatile compounds have been identified by GC-MS, and their relative amounts have been calculated by adding internal standard to the samples. Differences in composition of lemon juices volatile components have been observed. Verdello Siracusano lemon juice has the highest amount of volatile compounds (50.28 mg/L), followed by Interdonato (8.39 mg/L), Primo Fiore Capo d'Orlando (5.75 mg/L), and Femminello Siracusano (2.62 mg/L) juices. Volatile compounds mainly consist of mono- and sesquiterpene hydrocarbons and oxygenated molecules (aldheydes, monoterpene alcohols, and monoterpene esters). Headspace solid phase microextraction coupled to a gas chromatograph equipped with a specific sulfur detector, a sulfur chemiluminescence detector, let us detect and quantify dimethyl sulfide compound at the microgram/liter level in lemon juices.     

Evaluation of polyphenolic and flavonoid compounds in honeybee-collected pollen produced in Spain

Polyphenolic content, flavonoid content, and free flavonoid aglycon compounds were determined in 11 samples of Spanish honeybee-collected pollen. Adequate extraction was obtained with ethyl acetate in the determination of free flavonoid aglycon. Recovery (>83.6%), within-run repeatability (<6.67%), between-run reproducibility (<8.73%), and detection limits (1.4--1.9 mg/kg) were satisfactory. A total of 15 compounds were separated with gradient reversed phase HPLC, and 13 were identified and quantified using diode array detector. The most predominant compounds were flavonoid glycosides, mainly flavonols. Eighty-two percent of the samples contained at least 14 of the phenolic components, primarily rutin, quercetin, myricetin, and trans-cinnamic acid as free aglycons. Total phenols were present, at levels of >0.85 g/100 g in the form of non-tannins, and flavonoids of >0.35 g/100 g, using spectrophotometric procedures. Rutin is the best identifier of free flavonoid aglycon compounds. A minimum quantity of 200 mg/kg of rutin is suggested to guarantee the nutritional and biological properties required in the European market.     

Changes during storage in conventional and ecological wine: phenolic content and antioxidant activity

Polyphenol content, free radical scavenging capacity, and changes during storage over 7 months in the dark were studied in ecological and conventional red and white wines. In red wines, the most changeable components during storage were the anthocyanins since during storage anthocyanins content decreased 88% in conventional wine and 91% in ecological wine. Initially, the total flavonol contents of the conventional and ecological red wines were 163.88 +/- 2.69 and 153.58 +/- 1.71 mg/L, respectively, and no significant variations occurred during storage. No differences in hydroxycinnamic acid derivatives content between conventional and ecological red and white wines were observed. The flavonol level in white wines was very low, as expected since these compounds are found in grape skin. The initial antioxidant activity was 5.37 +/- 0.14 and 5.82 +/- 0.31 mM equivalents Trolox for conventional and ecological red wines, respectively; no significant differences were observed (p = 0.2831), and these values were 7-8 times higher than the antioxidant activity observed in conventional and ecological white wine. In contrast with other studies, the total concentrations of phenolic compounds in conventional and ecological red and white wines were not related to antioxidant activity (p > 0.05). In red wines, no significant differences were observed in the antioxidant activity of ecological and conventional red wine (p = 0.28), while in white wine significant differences were observed in the antioxidant activity between conventional and ecological white wine (p = 0.006).     

Multivariate analysis of FTIR and ion chromatographic data for the quality control of tequila

Principal component analysis (PCA) was applied to the chromatographic and spectroscopic data of authentic Mexican tequilas (n = 14) and commercially available samples purchased in Mexico and Germany (n = 24). The scores scatter plot of the first two principal components (PC) of the anions chloride, nitrate, sulfate, acetate, and oxalate accounting for 78% of the variability allowed a classification between tequilas bottled in Mexico and overseas; however, no discrimination between tequila categories was possible. Mexican products had a significantly (p = 0.0014) lower inorganic anion concentration (range = 1.5-5.1 mg/L; mean = 2.5 mg/L) than the products bottled in the importing countries (range = 3.3-62.6 mg/L; mean = 26.3 mg/L). FTIR allowed a rapid screening of density and ethanol as well as the volatile compounds methanol, ethyl acetate, propanol-1, isobutanol, and 2-/3-methyl-1-butanol using partial least-squares regression (precisions = 5.3-29.3%). Using PCA of the volatile compounds, a differentiation between tequila derived from "100% agave" (Agave tequilana Weber var. azul, Agavaceae) and tequila produced with other fermentable sugars ("mixed"tequila) was possible. The first two PCs describe 89% of the total variability of the data. Methanol and isobutanol influenced the variability in PC1, which led to discrimination. The concentrations of methanol and isobutanol were significantly higher (methanol, p = 0.004; isobutanol, p = 0.005) in the 100% agave (methanol, 297.9 +/- 49.5; isobutanol, 251.3 +/- 34.9) than in the mixed tequilas (methanol, 197.8 +/- 118.5; isobutanol, 151.4 +/- 52.8).     

Volatile constituents from the leaves of Callicarpa japonica Thunb. and their antibacterial activities

Volatile substances of Callicarpa japonica Thunb. were examined for their antibacterial activities against six foodborne microorganisms using the optical densitometer Bioscreen C. Extracts of C. japonica were obtained by simultaneous steam distillation and solvent extraction (SDE), and those extracted for 1.5 and 2.0 h at pH 6.0 strongly inhibited the growth of Bacillus cereus and Salmonella typhimurium; the content of the volatile substances of leaves at these pH levels were 543.1 and 706.7 mg/kg, respectively. All foodborne microorganisms tested were strongly inhibited by the addition of >8% (v/v) of the SDE extracts to broth medium. The major volatile components of the SDE extracts obtained at 1.5 h and pH 6.0 were gamma-caryophyllene, 1-octen-3-ol, 2-hexenal, germacrene B, and aromadendrene II, with corresponding peak areas of 44.14, 15.6, 9.86, 5.24, and 4.01%, respectively, and major antibacterial components were 1-octen-3-ol and 2-hexenal. Among the 32 materials identified as volatile flavor components, 2-hexenal, 2,4-hexadienal, 1-octen-3-ol, 2,4-heptadienal, and epiglobulol strongly inhibited microorganism growth. In particular, 2-hexenal (107.52 mg/L) and 1-octen-3-ol (678.64 mg/L) inhibited the growth of most microorganisms tested by >90%.     

不同品种鲜食糯玉米清汁与籽粒中挥发性成分比较

为研究不同品种鲜食糯玉米香气成分之间的差异,本研究对6个品种糯玉米进行了清汁制作和煮制两种熟化生香处理,并采用顶空固相微萃取法结合气相色谱-质谱联用技术(HS-SPME-GC-MS)对其挥发性成分进行测定。结果表明,清汁中检出的挥发性成分数量和总量均高于籽粒:清汁中检出38种挥发性成分,熟粒中检出24种,其中仅在清汁中检出的成分中有7种为吡嗪类化合物;而各品种糯玉米清汁中检测到的挥发性成分总量是籽粒的3.98~10.92倍。主成分分析(PCA)结果显示,前两个主成分可解释清汁样品总方差的72.6%,高于煮制籽粒(60.9%),但两种PCA结果均显示JDN-517、SYN-602与SYN-11的特色值得关注,并与吡嗪以及醛醇类成分含量差异有关。本研究结果为不同品种鲜食糯玉米风味品质评价中的样品处理以及数据分析提供了一定的参考。     

Smoke-derived taint in wine: the release of smoke-derived volatile phenols during fermentation of Merlot juice following grapevine exposure to smoke

The release of smoke-derived volatile phenols during the fermentation of Merlot grapes, following grapevine exposure to smoke, has been investigated. The concentrations of guaiacol, 4-methylguaiacol, 4-ethylguaiacol, 4-ethylphenol, and eugenol were determined by gas chromatography-mass spectrometry and found to increase throughout the winemaking process. Only trace levels (< or = 1 microg/L) of guaiacol and 4-methylguaiacol could be detected in free run juice derived from the fruit of smoked vines; the highest levels, 388 microg/L and 93 microg/L, respectively, were observed in the finished wine. Control wine (derived from fruit of unsmoked vines) contained 4 microg/L guaiacol, with the volatile phenols either not detected or detected at only trace levels (< or = 1 microg/L) throughout fermentation. The role of enzyme and acid catalyzed hydrolysis reactions in releasing smoke-derived volatile compounds was also investigated. The volatile phenols were released from smoked free run juice by strong acid hydrolysis (pH 1.0) and enzyme (beta-glucosidase) hydrolysis, but not mild acid hydrolysis (juice pH 3.2-3.7). Guaiacol was again the most abundant smoke-derived phenol, present at 431 microg/L and 325 microg/L in strong acid and enzyme hydrolysates, respectively. Only trace levels of each phenol could be detected in each control hydrolysate. This study demonstrates the potential for under-estimation of smoke taint in fruit and juice samples; the implications for the assessment of smoke taint and quantification of volatile phenols are discussed.     

Sulfate--a candidate for the missing essential factor that is required for the formation of protein haze in white wine

Protein haze formation in white wine is dependent on the presence of both wine protein and other unknown wine components, termed factor(s) X. The ability to reconstitute protein haze upon heating artificial model wine solutions (500 mg/L thaumatin, 12% ethanol, 4 g/L tartaric acid) to which candidate components were added was employed to identify factor(s) X. No protein haze was formed in the absence of additives. The individual or combined addition of caffeic acid, caftaric acid, epicatechin, epigallocatechin-O-gallate, gallic acid, or ferulic acid at typical white wine concentrations did not generate protein haze. However, PVPP fining of commercial wines resulted in a reduction in protein haze, suggesting that phenolic compounds may play a modulating role in haze formation. To elucidate the nature of the unknown factor(s) wine was fractionated and fractions were back-added to model wine and tested for their essentiality. Wine fractions were generated by ultrafiltration, reverse-phase chromatography, and mixed-mode anion-exchange and reverse-phase chromatography. The only purified fraction containing the essential component(s) was free of phenolic compounds, and analysis by mass spectrometry identified sulfate anion as the dominant component. Reconstitution with KHSO4 using either commercially available thaumatin or wine proteins confirmed the role of sulfate in wine protein haze formation. The two main wine proteins, thaumatin-like protein and chitinase, differed in their haze response in model wines containing sulfate. Other common wine anions, acetate, chloride, citrate, phosphate, and tartrate, and wine cations, Fe(2+/3+) and Cu(+/2+), when added at typical white wine concentrations were not found to be essential for protein haze formation.     

Antioxidant capacities and phenolics levels of French wines from different varieties and vintages.

Phenolics from grapes and wines can play a role against oxidation and development of atherosclerosis. Levels of phenolics, major catechins [(+)-catechin, (-)-epicatechin, procyanidin dimers B1, B2, B3, and B4], phenolic acids (gallic acid and caffeic acid), caftaric acid, malvidin-3-glucoside, peonidin-3-glucoside, and cyanidin-3-glucoside were quantified by HPLC with UV detection for 54 French varietal commercial wines taken from southern France to study the antioxidant capacity and the daily dietary intake of these compounds for the French population. The highest antioxidant capacity was obtained with red wines and ranged from 12.8 mmol/L (Grenache) to 25.2 mmol/L (Pinot Noir). For white wines, Chardonnay enriched in phenolics by special wine-making was found to have an antioxidant capacity of 13.8 mmol/L, comparable to red wine values. For red wines classified by vintages (1996-1999) antioxidant capacities were approximately 20 mmol/L and then decreased to 13.4 mmol/L for vintages 1995-1991. Sweet white wines have 1.7 times more antioxidant capacity (3.2 mmol/L) than dry white wines (1.91 mmol/L). On the basis of a still significant French wine consumption of 180 mL/day/person, the current daily intake of catechins (monomers and dimers B1, B2, B3, and B4) averaged 5 (dry white wine), 4.36 (sweet white wines), 7.70 (rosé wines), 31.98 (red wines), and 66.94 (dry white wine enriched in phenolic) mg/day/resident for the French population. Red wine, and particularly Pinot Noir, Egiodola, Syrah, Cabernet Sauvignon, and Merlot varieties, or Chardonnay enriched in phenolics during wine-making for white varieties contribute to a very significant catechin dietary intake.     

蛋鸡舍臭气组成及不同管理措施对臭气特性的影响

随着中国蛋鸡养殖规模化的快速发展,蛋鸡场排出的臭气已成为影响周边环境质量的重要因素,但有限的关于蛋鸡舍臭气特性的研究严重制约着臭气污染程度的量化和除臭措施的制定,因此该研究通过对2种不同类型蛋鸡舍（商品蛋鸡舍和种用蛋鸡舍）的臭气进行综合分析,以探究不同管理措施（无管理操作、喂料、喷雾消毒、清粪）对臭气组成及其对臭气贡献率的影响。结果表明,2种类型蛋鸡舍的臭气组成和浓度相似,蛋鸡舍内臭气成分的浓度从高到低为NH3、挥发性脂肪酸（Volatile Fatty Acids,VFA）、挥发性含硫化合物（Volatile Sulfur Compounds,VSC）、酚类、吲哚类和胺类,对臭味贡献率从大到小为吲哚类、酚类、VSC、VFA、胺类和NH3。无管理操作和喂料过程中臭气组成和浓度相似,饲料的味道对蛋鸡舍臭气浓度影响较小。喷雾消毒和清粪过程中NH3、吲哚类和臭气浓度均显著增加（P<0.05）。此外,粪污在清粪带滞留期间,NH3浓度增加了6倍,胺类、VSC、吲哚类、酚类和VFA的浓度相对稳定。除NH3以外的其他成分主要来自肠道微生物的降解,对臭气贡献率高达99.99%,是臭味的主要来源。