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14 pages, 1803 KiB  
Article
Discovery of Potential Candidate Genes for Coat Colour in Wuzhishan Pigs by Integrating SNPs and mRNA Expression Analysis
by Qiao Xu, Yabiao Luo, Zhe Chao, Jibin Zhang, Xiaolei Liu, Danqin Tu, Qin Guo, Ruiping Sun, Feng Wang and Meiying Fang
Animals 2024, 14(23), 3493; https://doi.org/10.3390/ani14233493 - 3 Dec 2024
Viewed by 178
Abstract
Despite identifying genes regulating the coat colour in Western pig breeds, the genetic basis of the coat colour in Chinese indigenous pigs is still not understood due to the diversity of indigenous breeds and their genetic differences from exotic pigs. In this study, [...] Read more.
Despite identifying genes regulating the coat colour in Western pig breeds, the genetic basis of the coat colour in Chinese indigenous pigs is still not understood due to the diversity of indigenous breeds and their genetic differences from exotic pigs. In this study, 215 Wuzhishan pigs with three coat colour patterns (white, black, and black-back/white-belly) were used to conduct a genome-wide association analysis. We found that genes responsible for the coat colour in the Wuzhishan breed are located on chromosome 8. Ninety-seven genome-wide significant SNPs are related to the animal’s coat colour. Using a haplotype-sharing analysis, we narrowed the potential candidate region to a 10.1 Mb interval encompassing only one gene, RAPGEF2, which participates in the regulation of melanogenesis. Two additional candidate genes, PDGFRA and KIT, are located within 1 Mb of the genome-wide significant SNPs. Gene ontology analysis and literature mining suggest that these candidate genes are associated with the animal’s coat colour. mRNA expression results revealed that RAPGEF2 and PDGFRA had significantly higher expressions in black pigs than in white pigs and higher expressions in black skin than in white skin from the same black-back/white-belly pigs. These results suggest that RAPGEF2 and PDGFRA are potential candidate genes regulating the coat colour in Wuzhishan pigs. Interestingly, mutations of KIT (a gene duplication and a G to A substitution at the splicing site in intron 17) were detected in white Wuzhishan pigs but not in black-back/white-belly or black pigs, suggesting a close genetic relationship between white Wuzhishan pigs and Western white pig breeds. In summary, these results indicate that the expression of RAPGEF2 and PDGFRA may cause the coat colour variation by influencing the deposition of melanin, while the mutation of KIT causes the white coat colour. Our results may provide a theoretical basis for the breeding of white coat colour Wuzhishan pigs, and shed light on the complex genetic background of coat colour variations in indigenous Chinese pig breeds. Full article
(This article belongs to the Section Animal Genetics and Genomics)
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<p>Three coat colour phenotypes in Wuzhishan pigs. (<b>A</b>) white, (<b>B</b>) black-back/white-belly, (<b>C</b>) black.</p>
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<p>(<b>A</b>) Manhattan plot showing results from the genome-wide association study for coat colour traits in Wuzhishan pigs. (<b>B</b>) Quantile–quantile plot showing observed (black line) versus expected (blue points) log10 (<span class="html-italic">p</span>-values). The null hypothesis (no association between SNPs and coat colour) is represented by the red line.</p>
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<p>Fixation index (FST) plots generated using average FST values, with 500 Kb windows and 200 Kb overlap between adjacent windows. (<b>A</b>) FST plot for white vs. black. (<b>B</b>) FST plot for white vs. black-back/white-belly. (<b>C</b>) FST plot for black vs. black-back/white-belly. The horizontal red line indicates the top 1% FST values. SNPs with values above this threshold were considered to be selective sweep loci.</p>
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<p>Linkage disequilibrium (LD) plot generated by Haploview4.2 for SNPs in the 10.1 Mb region between the two most significant SNPs (DRGA0008593 and ALGA0047848) in SSC8. SNP IDs are indicated horizontally across the top. The black lines indicate the identified haplotype blocks containing significant SNPs with complete linkage disequilibrium. Red diamonds represent LD between two SNPs with r<sup>2</sup> values lower than 100% when labelled but that are equal to 100% when unlabelled.</p>
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<p>Expression of (<b>A</b>) <span class="html-italic">RAPGEF2</span> and (<b>B</b>) <span class="html-italic">PDGFRA</span> in skin tissues from Wuzhishan pigs exhibiting one of the three possible coat colours. Results are shown as means ± SD of triplicate measurements. * indicates <span class="html-italic">p</span> &lt; 0.05, ** indicates <span class="html-italic">p</span> &lt; 0.01. White belly and black back are both samples from black-back/white-belly pigs.</p>
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<p>The G to A mutation located at the first nucleotide in intron 17 of <span class="html-italic">KIT</span>, which causes alternative splicing, was detected through sequencing and restriction digestion. (<b>A</b>) Sequence alignment of data obtained from pooled DNA samples (from 30 individuals) shows the mutation in <span class="html-italic">KIT</span> intron 17. The red column highlights the mutation site (93G &gt; A); Yorkshire and white Wuzhishan pigs exhibit double peaks, indicating nucleotides G and A at that location, while all the other pigs showed single peaks at this location, indicating the presence of only G nucleotide. (<b>B</b>) Agarose gel displaying the PCR product from <span class="html-italic">KIT</span> intron 17 of Wuzhishan pigs after digestion with NlaIII. Lanes 1–3 contain DNA from white pigs, 4–6 from black-back/white-belly pigs, and 7–9 from black pigs. The three bands in the Yorkshire and white pig lanes are diagnostic of the splice mutation, while the double bands are wild type. The Yorkshire and Rongchang pigs served as positive and negative controls, respectively.</p>
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13 pages, 2000 KiB  
Article
Convective Drying with the Application of Ultrasonic Pre-Treatment: The Effect of Applied Conditions on the Selected Properties of Dried Apples
by Ewa Jakubczyk, Katarzyna Rybak, Dorota Witrowa-Rajchert, Artur Wiktor, Rafał Rąbkowski and Małgorzata Nowacka
Foods 2024, 13(23), 3893; https://doi.org/10.3390/foods13233893 - 3 Dec 2024
Viewed by 262
Abstract
The aim of this study was to evaluate the effect of ultrasound used as a preliminary treatment and drying temperature on the properties of dried apples (var. Golden Delicious). The aim of the work was also to optimise the process in terms of [...] Read more.
The aim of this study was to evaluate the effect of ultrasound used as a preliminary treatment and drying temperature on the properties of dried apples (var. Golden Delicious). The aim of the work was also to optimise the process in terms of reducing the drying time and obtaining a product with specific properties. The apple tissue was sonicated for various times from 30 to 60 min. Then, the tissue was air-dried with a constant air flow of 55 to 85 °C. The work determined the dry substance content, water activity, colour parameters, content, antioxidant activity, and hygroscopicity of the dried material. The drying kinetics were also analysed. The results showed that the decrease in sonification time increased the dry matter content and reduced water activity. Also, the decrease in drying temperature caused a smaller intake of water and led to a lower hygroscopicity of dried apples. The selected parameters of the process had a positive effect on the preservation of bioactive compounds and led to an increase in antioxidant activity. Experimental results were adapted by a second-order polynomial model, where analysis of variance was utilized to define optimal drying conditions. Therefore, considering the shortest drying time, the lowest colour difference, ΔE, and the highest antioxidant activity, the best condition for the drying of apple tissue can be obtained with the application of 30 min of samples sonication and drying of apples at a temperature of 80.9 °C. Full article
(This article belongs to the Special Issue New Methods in Food Processing and Analysis)
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Graphical abstract

Graphical abstract
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<p>Effect of US pre-treatment and drying temperature on (<b>a</b>) EC 50 ABTS and (<b>b</b>) Polyphenols content of dried apples. T-55, T-70, T-80: drying temperature of 50, 70, and 80 °C. US30, US45, US60: sonification time of 30, 45, and 60 min. The different letters indicate the significant difference between the values in the bars.</p>
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<p>Drying curves of dried apples with and without ultrasonic pre-treatment. T-55, T-70, T-80: drying temperature of 50, 70, and 80 °C. US30, US45, US60: sonification time of 30, 45, and 60 min.</p>
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<p>Response surface plots of some selected attributes: (<b>a</b>) dry matter; (<b>b</b>) water activity, (<b>c</b>) hygroscopicity (water content after 24 h of sorption), (<b>d</b>) EC<sub>50</sub> ABTS, (<b>e</b>) drying time depending on the drying temperature and time of US pre-treatment of apples.</p>
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<p>Response plot for desirability of dried apples as a function of drying temperature and time of ultrasonic pre-treatment.</p>
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21 pages, 4268 KiB  
Article
Shelf Life and Organoleptic Attributes of Multifruit Smoothies Treated by Combined Mild Preservation Technologies
by Fanni Zakariás, Karina Ilona Hidas, Zoltan Kovacs, György Bázár, Andrea Taczman-Brückner, István Dalmadi and Gabriella Kiskó
Appl. Sci. 2024, 14(23), 11223; https://doi.org/10.3390/app142311223 - 2 Dec 2024
Viewed by 316
Abstract
The application of high hydrostatic pressure and mild heat treatment represents preservation processes for extending the shelf life of food products without compromising their quality. The combination of these physical methods at lower applied levels represents a promising approach to preserving the quality [...] Read more.
The application of high hydrostatic pressure and mild heat treatment represents preservation processes for extending the shelf life of food products without compromising their quality. The combination of these physical methods at lower applied levels represents a promising approach to preserving the quality of treated products. This study aims to investigate the impact of combined treatments on the quality and storage stability of strawberry, banana, almond milk and avocado smoothies. The total colony count, electronic nose and tongue signals, colour, viscosity and sensory properties were examined over a 14-day storage period at 6 °C. The combined treatments were found to be effective in reducing the total colony count. During the sensory analysis, the impact of storage was the most prominent factor. Both the treatments and storage conditions significantly affected the colour characteristics of the samples. The smoothie samples exhibited pseudoplastic flow behaviour. Both applied treatments resulted in enhanced texture stability of the samples during the storage period. The electronic tongue and nose could differentiate between groups of fresh and stored samples, as well as between control and treated samples. Full article
(This article belongs to the Special Issue Advanced Technologies for Food Packaging and Preservation)
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<p>Total colony count of smoothie samples. A, B: comparison of fresh samples treated with different methods (Tukey’s post hoc test, <span class="html-italic">p</span> &lt; 0.05); a, b, c: comparison of samples stored at 6 °C for 14 days and treated by different methods (Tukey’s post hoc test, <span class="html-italic">p</span> &lt; 0.05); *, **, ***: comparison of samples stored at 15 °C for 14 days and treated by different methods (Tukey’s post hoc test, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Flow curves (<b>a</b>) and viscosity curves (<b>b</b>) of tested smoothie samples on days 0 and 14.</p>
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<p>Mean and standard deviation of the selected six electronic tongue sensor signals of the tested smoothie samples (<span class="html-italic">n</span> = 36).</p>
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<p>Euclidean distances calculated between the raw signals of the selected six electronic tongue sensors of the tested smoothie samples (<span class="html-italic">n</span> = 36); a neuron-like graph for the visualisation of the Euclidean distances.</p>
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<p>PCA score and loadings plots of the electronic tongue measurements of the tested smoothie samples. (<b>a</b>) PCA score plot (PC1-PC2) coloured by sample types, (<b>b</b>) PCA score plots (PC1-PC3) coloured by the applied pressure level, storage, and treatment types, respectively, and (<b>c</b>) PCA loadings plot (<span class="html-italic">n</span> = 36).</p>
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<p>Chromatograms recorded on the two columns of the Heracles Neo 300 electronic nose for one representative sample of each group. (<b>a</b>) Fresh samples, column 1-A, (<b>b</b>) samples 14th day, column 1-A, (<b>c</b>) fresh samples, column 2-A, (<b>d</b>) samples 14th day, column 2-A.</p>
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<p>Score plot of the principal component analysis performed with all virtual sensors of the electronic nose.</p>
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<p>Result of the discriminant factor analysis performed with all virtual sensors of the electronic nose.</p>
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<p>The average intensity values and standard deviations (dashed area) of the most distinctive virtual sensors for the six groups of samples.</p>
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<p>Result of the discriminant factor analysis performed with the selected virtual sensors indicating the impact of each sensor on the classification performance (the asterisks indicate the size of the vectors showing the effect of each sensor).</p>
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15 pages, 7063 KiB  
Article
In Operando Optical Analysis of Electrolyte Colour Change and Its Correlation to Capacity Fade in Li-Ion Cells at Elevated Temperatures
by Saud Sattar, Thomas Statheros, Ali Raza, Quirin Kellner, Yifei Yu, Rohit Bhagat, Alexander J. Roberts and Yue Guo
Sensors 2024, 24(23), 7686; https://doi.org/10.3390/s24237686 (registering DOI) - 30 Nov 2024
Viewed by 430
Abstract
The existing body of research on battery state of health has identified various degradation modes for the electrolyte, yet very few studies have explored the role of electrolyte colour changes as a diagnostic tool for state of health (SOH). This study investigates the [...] Read more.
The existing body of research on battery state of health has identified various degradation modes for the electrolyte, yet very few studies have explored the role of electrolyte colour changes as a diagnostic tool for state of health (SOH). This study investigates the impact of elevated temperatures and its correlation with electrolyte colour changes and capacity fade during cycling. Specifically, the research examines whether cycling cells at elevated temperatures induces noticeable changes in electrolyte colour and whether these changes can be linked to the SOH of the cells. The methodology employs in operando optical sensors to monitor real-time colour shifts in the electrolyte, aiming to demonstrate a qualitative relationship between electrolyte colour change, degradation, thermal ageing, and capacity fade, laying the foundations for future quantitative assessment of the relationships identified. Our research builds upon these findings by offering a novel approach that integrates optical sensing to provide real-time visual evidence of electrolyte degradation and colour change during cell operation. The results demonstrate a clear relationship between elevated temperature, electrolyte colour change, and capacity fade, leading to accelerated degradation. This approach offers a new insight over traditional in exitu battery diagnostics, as it enables continuous in operando monitoring of electrolyte colour change and has the potential to unlock a detailed understanding of the chemical reactions and electrolyte breakdown during cycling. Full article
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<p>A foldable design of the photodiode and LED [<a href="#B2-sensors-24-07686" class="html-bibr">2</a>].</p>
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<p>Formation profiles for Cell25, Cell40, and Cell55.</p>
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<p>Capacity fade analysis for Cells 55, 40, and 25 vs cell cycle #.</p>
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<p>RGB values and capacity with the cycling number, with a visual representation of colours represented in the columns in the bar graph at 25 °C cycling.</p>
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<p>RGB values and capacity with the cycling number, with a visual representation of colours represented in the columns in the bar graph at 40 °C cycling.</p>
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<p>RGB values and capacity with the cycling number, with a visual representation of colours represented in the columns in the bar graph at 55 °C cycling.</p>
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<p>Change in blue LED intensity for Cell55, Cell40, and Cell25.</p>
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<p>Differential analysis of change in blue intensity for Cell55, Cell40, and Cell25.</p>
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<p>Change in green LED intensity for Cell55, Cell40, and Cell25.</p>
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<p>Differential analysis of change in green intensity for Cell55, Cell40, and Cell25 vs. cell cycle #.</p>
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<p>Change in red LED intensity for Cell55, Cell40, and Cell25.</p>
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<p>Differential analysis of change in red intensity for Cell55, Cell40, and Cell25.</p>
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16 pages, 6620 KiB  
Article
Exploiting Bacterial Pigmentation for Non-Destructive Detection of Seed-Borne Pathogens by Using Photoacoustic Techniques
by Lucia Cavigli, Dario Gaudioso, Cecilia Faraloni, Giovanni Agati and Stefania Tegli
Sensors 2024, 24(23), 7616; https://doi.org/10.3390/s24237616 - 28 Nov 2024
Viewed by 237
Abstract
Seed-borne pathogens pose a significant threat to global food security. This study focuses on Curtobacterium flaccumfaciens pv. flaccumfaciens (Cff), a quarantine plant pathogen causing bacterial wilt of common beans. Despite its global spread and economic impact, effective control measures are limited. [...] Read more.
Seed-borne pathogens pose a significant threat to global food security. This study focuses on Curtobacterium flaccumfaciens pv. flaccumfaciens (Cff), a quarantine plant pathogen causing bacterial wilt of common beans. Despite its global spread and economic impact, effective control measures are limited. Existing diagnostic methods, such as PCR, are time-consuming, destructive, and challenging for large-scale screening. This study explores the potential of photoacoustic techniques as a non-destructive, rapid, and high-throughput alternative. These techniques leverage the photoacoustic effect to measure optical absorption, offering high sensitivity and accuracy. Cff colonies exhibit distinct pigmentation, suggesting their suitability for photoacoustic detection. We characterised the optical properties of Cff and developed an in vitro model to simulate conditions within Cff-infected bean seeds. The results demonstrate the efficiency of the photoacoustic technique in detecting Cff in a mimicked-bean seed and indicate the potential discrimination of different coloured Cff strains. This study paves the way for a novel, non-invasive approach to the early detection of Cff and other seed-borne pathogens, contributing to improve crop health and food security. Full article
(This article belongs to the Special Issue Photonics for Advanced Spectroscopy and Sensing)
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<p><span class="html-italic">Cff</span> strains grown on naturalised media, based on Cannellino (<b>left</b>) and on Borlotto bean flour (<b>right</b>).</p>
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<p>HPLC chromatograms of the methanolic extracts of <span class="html-italic">Cff</span> P990 (<b>a</b>), <span class="html-italic">Cff</span> 50R (<b>b</b>), and <span class="html-italic">Cff</span> C7 (<b>c</b>) pigments, after 14 days of growth on Cannellino naturalised medium. Different symbols mark the peak with different absorbance spectra corresponding to C.p. 450 (*), C.p. 473 (+), and C.p. 496 (∧) compounds. Spectra of the main peaks, acquired during elution in methanol, are reported in (<b>d</b>–<b>f</b>) for <span class="html-italic">Cff</span> P990, <span class="html-italic">Cff</span> 50R, and <span class="html-italic">Cff</span> C7, respectively.</p>
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<p>(<b>a</b>) Total transmittance spectra from the Cannellino- (black line) and the Borlotto-based media (red line). Comparison of the overall transmittance signal at 485 nm (<b>b</b>) and at 800 nm (<b>c</b>) between Cannellino- (black line) and Borlotto-based (red line) media. (<b>d</b>) Comparison of the PA amplitude between Cannellino- (black line) and Borlotto-based (red line) media excited by the whole laser white emission.</p>
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<p>PA signal vs. time of arrival to the transducer from the Cannellino naturalised medium, after the excitation with the full laser emission (red lines), and with the laser emission filtered by the KG3 filter (black lines) at four different sample zones: (<b>a</b>) uninoculated point, (<b>b</b>) <span class="html-italic">Cff</span> P990 strain spot, (<b>c</b>) <span class="html-italic">Cff</span> 50R strain spot, and (<b>d</b>) <span class="html-italic">Cff</span> C7 strain spot.</p>
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<p>PA signal vs. time of arrival to the transducer from the Borlotto naturalised medium, after the excitation with the full laser emission (red lines), and with the laser emission filtered by the KG3 filter (black lines) at four different sample zones: (<b>a</b>) uninoculated point, (<b>b</b>) <span class="html-italic">Cff</span> P990 strain spot, (<b>c</b>) <span class="html-italic">Cff</span> 50R strain spot, and (<b>d</b>) <span class="html-italic">Cff</span> C7 strain spot.</p>
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<p>PA signal vs. time of arrival at different excitation wavebands defined by the laser emission spectrum combined with long-pass (LP) filters (at cut-on wavelengths of 475, 515, 550, and 590 nm) from spots of the P990 (<b>a</b>,<b>d</b>), 50R (<b>b</b>,<b>e</b>), and C7 (<b>c</b>,<b>f</b>) <span class="html-italic">Cff</span> strain grown in the Cannellino (<b>a</b>–<b>c</b>) or Borlotto naturalised media.</p>
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<p>(<b>a</b>–<b>c</b>) Amplitude of the bacterial PA signal (red circles) and the <math display="inline"><semantics> <msub> <mi>A</mi> <mi>eff</mi> </msub> </semantics></math> (black squares) of <span class="html-italic">Cff</span> pigments as a function of the excitation waveband. Wavebands are identified by the cut-on wavelengths of the long-pass filters from 475 nm to 630 nm. Each set of data is normalised to the first point at 440 nm corresponding to the measurement with the whole laser emission excitation.</p>
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20 pages, 3532 KiB  
Article
Development of Innovative Environmental Safety: Bioactives Against Pathogenic Bacteria Red Pectin Films from Hibiscus sabdariffa Flos Extract for Circular Economy
by Marcin Szymański, Jolanta Długaszewska, Mikołaj Pawlik and Renata Dobrucka
Coatings 2024, 14(12), 1500; https://doi.org/10.3390/coatings14121500 - 28 Nov 2024
Viewed by 390
Abstract
In this work, we developed an antioxidant and antibacterial red pectin food packaging material with natural Hibiscus sabdariffa flos. This study showed that this red pectin film (PJH, PCH, PCJH) containing Hibiscus extract exhibited antioxidant activity. The addition of hibiscus improved the barrier [...] Read more.
In this work, we developed an antioxidant and antibacterial red pectin food packaging material with natural Hibiscus sabdariffa flos. This study showed that this red pectin film (PJH, PCH, PCJH) containing Hibiscus extract exhibited antioxidant activity. The addition of hibiscus improved the barrier properties. The WVTR parameter values for the PJH, PCH and PJCH samples were as follows: 4.87 [g/m2d], 4.45 [g/m2d], and 4.48 [g/m2d]. The addition had a significant effect on the L* of the samples, i.e., PJH, PCH and PJCH films. This is a useful effect for films of selected products or product groups. Microbiological analyses of our red pectin films showed that they had an inhibitory effect on the growth of Listeria monocytogenes. In the case of the Staphylococcus aureus strain, the inhibitory effect was shown by films that contained hibiscus extract: PJH, PCH and PJCH. This means that the added hibiscus increased the antimicrobial activity of our red films. An additional advantage of our pectin films is their red colour, which, in addition to its protective and ecological function, also plays a marketing role. Full article
(This article belongs to the Special Issue Advanced Coatings and Films for Food Packing and Storage, 2nd Edition)
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<p>Films of PJO: (<b>A</b>) (apple pectin) and PJH (<b>B</b>) (apple pectin hibiscus extract).</p>
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<p>Structures of the main compounds identified in <span class="html-italic">Hibiscus sabdariffa</span> flos ethanol extract: (<b>A</b>) cyclopentanecarboxylic acid, 2-oxo-, ethyl ester, (<b>B</b>) cyclohexanecarboxylic acid ethyl ester and (<b>C</b>) Linoleic acid ethyl ester.</p>
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<p>FTIR spectra for red pectin food packaging material.</p>
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<p>Diagram demonstrating the difference in the number of microorganisms (LF) after 24 h of incubation on the surface of the test films and the initial number of microorganisms expressed in log10. LF—Difference in the number of microorganisms after 24 h of incubation on the surface of the tested films and the initial number of microorganisms expressed in log10.</p>
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<p>The graph showing the WVTR for the tested films.</p>
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<p>Diagrams of the dependence of mass loss during the dissolution of films in solutions of different pH values on dissolution time.</p>
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<p>Diagrams of extract activity relationships for individual samples: (<b>A</b>) rape, (<b>B</b>) lupine and (<b>C</b>) dill.</p>
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<p>SEM images for the tested red foils: PJO, PCO, PJCO, PJH, PCH and PJCH.</p>
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11 pages, 3469 KiB  
Article
Resolving Visible Emission Lines in Hydrogen Diffusion Flames
by Muyi Pan, Xuanqi Liu, Yufeng Lai, Yuchen Zhang and Yang Zhang
Aerospace 2024, 11(12), 983; https://doi.org/10.3390/aerospace11120983 - 28 Nov 2024
Viewed by 302
Abstract
The hydrogen diffusion flame is commonly described as difficult to see in the visible range. However, even in controlled laboratory conditions with careful imaging, the flame appears reddish. Previous research has reported a variety of colours generated from hydrogen flames. Some researchers believe [...] Read more.
The hydrogen diffusion flame is commonly described as difficult to see in the visible range. However, even in controlled laboratory conditions with careful imaging, the flame appears reddish. Previous research has reported a variety of colours generated from hydrogen flames. Some researchers believe that the visible colour is due to sodium in airborne dust. Other studies suggest the flame colour is caused by the vibration–rotation band of water vapour. In addition, Hα emits radiance in the visible range; therefore, the visible colour of the hydrogen flame could be contributed from the Hα emission. Nevertheless, a definitive conclusion to explain the visible reddish colour of the hydrogen flame is lacking. This paper reports precisely instrumented spectroscopic imaging tests, calibration, and data processing in order to resolve the spectral lines in the red colour zone (580–700 nm). This study used a spectrograph and a DSLR camera to capture the spectrum of hydrogen diffusion flames under different co-flow conditions. The values of emission lines in this range were compared with the databases provided by HITRAN molecular spectroscopy and the National Institute of Standards and Technology (NIST). The results of this study show that Hα emission is highly likely to appear in a hydrogen diffusion flame, which contradicts the previous hypothesis. This work may provide new insight into hydrogen-based combustion. Full article
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<p>The flame spectrum of oxygen burning in hydrogen in the range from 610 nm to 730 nm, captured by Gaydon [<a href="#B3-aerospace-11-00983" class="html-bibr">3</a>].</p>
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<p>Hydrogen diffusion flame experimental setup with close-up showing the gas flow from the nozzle.</p>
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<p>Hydrogen diffusion flame from a Bunsen burner: (<b>a</b>) unfiltered; (<b>b</b>) filtered.</p>
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<p>Hydrogen–air diffusion flame spectrum.</p>
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<p>Hydrogen diffusion flame spectrum plot (“*” indicates that the molecule is in an excited state).</p>
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<p>Spectrum plot of hydrogen–air diffusion flames with 3 L/min hydrogen flow rates and (<b>a</b>) 6.5 L/min air co-flow; (<b>b</b>) 13.0 L/min air co-flow; (<b>c</b>) 0.30 L/min oxygen co-flow; and (<b>d</b>) 0.55 L/min oxygen co-flow. The red arrows indicated the emission lines only appear in the spectra of hydrogen flames with oxygen co-flow and 13.0 L/min air co-flow, while the blue arrows indicated the emission lines only appear in the spectra of hydrogen flames with air co-flow.</p>
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<p>Spectrum plot of hydrogen–air diffusion flames with 3 L/min hydrogen flow rates and (<b>a</b>) 6.5 L/min air co-flow; (<b>b</b>) 13.0 L/min air co-flow; (<b>c</b>) 0.30 L/min oxygen co-flow; and (<b>d</b>) 0.55 L/min oxygen co-flow. The red arrows indicated the emission lines only appear in the spectra of hydrogen flames with oxygen co-flow and 13.0 L/min air co-flow, while the blue arrows indicated the emission lines only appear in the spectra of hydrogen flames with air co-flow.</p>
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17 pages, 3012 KiB  
Review
Preparation of Iron-Based Nanozymes and Their Application in Water Environment: A Review
by Xingfeng Cao, Gongduan Fan, Shiyun Wu, Jing Luo, Yuhan Lin, Weixin Zheng, Shuangyu Min and Kai-Qin Xu
Water 2024, 16(23), 3431; https://doi.org/10.3390/w16233431 - 28 Nov 2024
Viewed by 353
Abstract
Nanozymes represent a new generation of artificial enzymes that combine nanomaterial properties with catalytic activities similar to those of natural enzymes. It has significant advantages in catalytic efficiency, selectivity, and stability, leading to increasing interest in their application in aqueous environments. Since the [...] Read more.
Nanozymes represent a new generation of artificial enzymes that combine nanomaterial properties with catalytic activities similar to those of natural enzymes. It has significant advantages in catalytic efficiency, selectivity, and stability, leading to increasing interest in their application in aqueous environments. Since the discovery of enzyme-like activity in Fe3O4, more and more iron-based nanozymes have been utilised for the detection and removal of pollutants. Iron is a non-toxic, low-cost transition metal, and this property makes iron-based nanozymes more compatible with safety requirements in aqueous environmental applications. Although iron-based nanozymes have demonstrated significant advantages in the water environment field, the relevant research is still in its infancy. Therefore, it is of great practical significance to systematically summarise the latest applications of iron-based nanozymes in the water environment. This paper describes the common methods of synthesising iron-based nanozymes. In addition, the applications of iron-based nanozymes in detecting pollutants and pollutant removal are reviewed. It was found that the removal of pollutants by iron-based nanozymes was mainly achieved through the reactive oxygen species, whereas the recognition of pollutants primarily depended on the reactions of iron-based nanozymes, such as colour development, fluorescence, and chemiluminescence. Finally, we highlight the challenges and future prospects for the application of iron-based nanozymes in water environments. In summary, this paper systematically summaries and discusses the common synthesis methods of iron-based nanozymes and their applications in the aquatic environment, with a view to providing new ideas for overcoming the limitations of traditional pollutant detection and removal methods and realising the high-quality development of iron-based nanozymes in water environment. Full article
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<p>Schematic diagram of the preparation process of (<b>a</b>) Fe-MoS<sub>2</sub> nanozyme [<a href="#B45-water-16-03431" class="html-bibr">45</a>] and (<b>b</b>) MIL-88B (Fe, Ni) nanozyme [<a href="#B51-water-16-03431" class="html-bibr">51</a>].</p>
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<p>Pollutant degradation mechanism diagram of (<b>a</b>) FeCu-NC nanozyme [<a href="#B68-water-16-03431" class="html-bibr">68</a>], (<b>b</b>) Fe<sub>3</sub>O<sub>4</sub>@N-HollCS nanozyme [<a href="#B69-water-16-03431" class="html-bibr">69</a>], (<b>c</b>) FeMn/N-CNTs nanozyme [<a href="#B70-water-16-03431" class="html-bibr">70</a>], and (<b>d</b>) Fe<sub>3</sub>O<sub>4</sub>@CeO<sub>2</sub>/Tb-MOF nanozyme [<a href="#B71-water-16-03431" class="html-bibr">71</a>].</p>
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<p>Pollutant detection mechanism diagram of (<b>a</b>) NH<sub>2</sub>-MIL-101(Fe)@Cu/CeO<sub>2</sub> nanozyme [<a href="#B91-water-16-03431" class="html-bibr">91</a>] and (<b>b</b>) NH<sub>2</sub>-MIL-101(Fe) nanozyme [<a href="#B92-water-16-03431" class="html-bibr">92</a>].</p>
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23 pages, 8972 KiB  
Article
Changes in Physical Attributes, Activities of Fruit Softening Enzymes, Cell Wall Polysaccharides and Fruit Quality of Jackfruit (Artocarpus heterophyllus Lam.) as Influenced by Maturation and Ripening
by Jashanpreet Kaur, Zora Singh, Muhammad Sohail Mazhar, Hafiz Muhammad Shoaib Shah and Andrew Woodward
Horticulturae 2024, 10(12), 1264; https://doi.org/10.3390/horticulturae10121264 - 28 Nov 2024
Viewed by 362
Abstract
Changes in physicochemical parameters, fruit softening enzymes and cell wall polysaccharides at four different maturation stages were investigated in two jackfruit genotypes (‘Accession 242’, ‘Accession 341’). For the first three maturity stages, fruit were harvested at 90, 110, and 130 days after flowering [...] Read more.
Changes in physicochemical parameters, fruit softening enzymes and cell wall polysaccharides at four different maturation stages were investigated in two jackfruit genotypes (‘Accession 242’, ‘Accession 341’). For the first three maturity stages, fruit were harvested at 90, 110, and 130 days after flowering (Stage I, II and III, respectively), while Stage IV was determined based on the presence of a dull hollow tapping sound. The fruit edible portion and seed percentage increased, whilst the core and rag percentage decreased with advancement in fruit maturation and ripening. The fruit harvested at Stage IV had comparatively higher soluble solids content (SSC), ascorbic acid and flavonoids, along with lower titratable acidity (TA) and phenolics, than other maturity stages. Bulb firmness was higher at Stage I in both genotypes, along with higher total pectin, protopectin and cellulose compared to other maturity stages. The activity of cell wall hydrolases was higher during later maturity stages. Fruit harvested at Stage IV had higher edible portions, carotenoids, flavonoids and SSC, as well as better colour attributes, while those harvested at Stage I exhibited higher phenolics, TA, pectin and cellulose. These findings could serve as a baseline for future research related to the intended use and maturity standardisation of jackfruit. Full article
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<p>Average monthly temperature and rainfall at Coastal Plains Research Farm, NT [<a href="#B18-horticulturae-10-01264" class="html-bibr">18</a>].</p>
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<p>Changes in size and colour of fruit (<b>A</b>) bulb (<b>B</b>) transverse section of fruit (<b>C</b>) and seeds (<b>D</b>) during fruit maturation and ripening of jackfruit ‘Accession 242’.</p>
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<p>Changes in size and colour of fruit (<b>A</b>) bulb (<b>B</b>) transverse section of fruit (<b>C</b>) and seeds (<b>D</b>) during fruit maturation and ripening of jackfruit ‘Accession 341’.</p>
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<p>Changes in fruit weight (<b>A</b>,<b>B</b>), fruit length (<b>C</b>,<b>D</b>) and fruit breadth (<b>E</b>,<b>F</b>) during fruit maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Changes in bulb weight (<b>A</b>,<b>B</b>), bulb length (<b>C</b>,<b>D</b>) and bulb breadth (<b>E</b>,<b>F</b>) during fruit maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Changes in seed weight (<b>A</b>,<b>B</b>), seed length (<b>C</b>,<b>D</b>) and seed breadth (<b>E</b>,<b>F</b>) with fruit maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05). Seed weight, length and breadth were recorded on 10 seeds per replication and then averaged for each replication (<span class="html-italic">n</span> = 3).</p>
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<p>Changes in edible portion (<b>A</b>,<b>B</b>), rag percentage (<b>C</b>,<b>D</b>), core percentage (<b>E</b>,<b>F</b>), peel percentage (<b>G</b>,<b>H</b>) and seed percentage (<b>I</b>,<b>J</b>) during fruit maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Changes in bulb chromaticity values <span class="html-italic">L*</span> (<b>A</b>,<b>B</b>), <span class="html-italic">a*</span> (<b>C</b>,<b>D</b>), <span class="html-italic">b*</span> (<b>E</b>,<b>F</b>), <span class="html-italic">C*</span> (<b>G</b>,<b>H</b>), and <span class="html-italic">h</span>° (<b>I</b>,<b>J</b>) during maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non-significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05). Bulb colour was recorded on three bulbs per replication and then the average was calculated for each replication (<span class="html-italic">n</span> = 3). <span class="html-italic">L*</span> = lightness; <span class="html-italic">a*</span> = ranging from green [-] to red [+]; <span class="html-italic">b*</span> = ranging from blue [-] to yellow [+]; <span class="html-italic">C*</span> = chroma; <span class="html-italic">h</span>° = hue angle.</p>
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<p>Changes in soluble solids content (<b>A</b>,<b>B</b>), titratable acidity (<b>C</b>–<b>F</b>) and SCC: TA (<b>G</b>,<b>H</b>) during fruit maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non-significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Changes in the levels of ascorbic acid (<b>A</b>,<b>B</b>), total carotenoids (<b>C</b>,<b>D</b>), total phenolics (<b>E</b>,<b>F</b>), total flavonoids (<b>G</b>,<b>H</b>) and DPPH radical scavenging activity (<b>I</b>,<b>J</b>) during maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Changes in bulb firmness (<b>A</b>,<b>B</b>), activities of polygalacturonase (<b>C</b>,<b>D</b>), pectin methyl esterase (<b>E</b>,<b>F</b>), pectate lyase (<b>G</b>,<b>H</b>) and cellulase (<b>I</b>,<b>J</b>) during maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05). Bulb firmness was recorded on three bulbs per replication and then averaged for each replication (<span class="html-italic">n</span> = 3).</p>
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<p>Changes in the levels of total pectin (<b>A</b>,<b>B</b>), water−soluble pectin (<b>C</b>,<b>D</b>), sodium carbonate soluble pectin (<b>E</b>,<b>F</b>), chelate soluble pectin (<b>G</b>,<b>H</b>), protopectin (<b>I</b>,<b>J</b>) and cellulose (<b>K</b>,<b>L</b>) during maturation and ripening of jackfruit ‘Accession 242’ and ‘Accession 341’. Vertical bars show the standard deviation of means (<span class="html-italic">n</span> = 3). Means with the same letters represent non−significant differences by LSD test (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Principal component biplots displaying the correlation between fruit physical attributes, biochemical parameters, antioxidants, activities of fruit softening enzymes and cell wall polysaccharides in bulbs during different stages of fruit maturation and ripening of jackfruit ‘Accession 242’ (<b>A</b>,<b>B</b>) and ‘Accession 341’ (<b>C</b>,<b>D</b>).</p>
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16 pages, 4717 KiB  
Article
Evaluation of the Visual Perception of Urban Single/Double-Layer Riverfront Greenway Landscapes Based on Deep Learning
by Xin Li, Yuan Wang, Zhenyu Wang and Qi Ding
Sustainability 2024, 16(23), 10391; https://doi.org/10.3390/su162310391 - 27 Nov 2024
Viewed by 401
Abstract
Urban inland rivers are closely related to urban development, but high-density urbanisation has reduced the natural function of streams and the riverbanks are hardened into two parts, embankment walls and berms, which give rise to a variety of riparian landscapes. However, the difference [...] Read more.
Urban inland rivers are closely related to urban development, but high-density urbanisation has reduced the natural function of streams and the riverbanks are hardened into two parts, embankment walls and berms, which give rise to a variety of riparian landscapes. However, the difference in the height of riparian walkways affects the degree of their greening and landscape effects. In this paper, we studied single- and double-decker urban greenways, constructed quantitative indicators of spatial elements based on deep learning algorithms using an image semantic segmentation (ISS) model that simulates human visual perception, used random forests and multivariate linear regression models to study the impact of the height difference of the linear riverfront greenway on visual perception, clarified the impact of the visual landscape differences caused by different types of space on landscape aesthetic preferences (LP) and confirmed the impact of the specific extent to which landscape components influence preferences. The results of the study showed that there were significant differences in landscape perception scores between the single and double layers. (1) The influence of WED (negative correlation) and NI (positive correlation) is large in the single-layer greenway. The colour, material and structure of the guardrail can be beautified and diversified and the quality of the greenery can be taken into account to maintain the visibility of the greenery in order to improve the score of the single-layer greenway. (2) The significant influence of BVI in the double-layered greenway is positive. Water-friendly or water-viewing spaces can be added appropriately to improve the landscape score of double-layered greenways. This study is applicable to the regional landscape feature identification of single- and double-decker greenways on large-scale urban hard barge bank images, which realises the whole-region feature identification of a large-scale human perspective and is an effective expansion of analysis techniques for sustainable landscape planning and the design of riparian greenways. Full article
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<p>Study area and typical characteristics of single- and double-decker greenways. (<b>a</b>) Comparison of typical real-life views of single- and double-decker greenways. (<b>b</b>) Typical characteristics of single- versus double-layered channels. (<b>c</b>) Typical characteristics of single- and double-decker greenways.</p>
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<p>Comparison of visual landscape scores for single- and double-decker greenways. (<b>a</b>): Box plot of the comparison of visual landscape scores for single- and double-decker greenways; (<b>b</b>): Distribution of visual landscape score results.</p>
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<p>Importance ranking of indicator items and correlation fitting results of important indicators for single-layer greenways. (<b>a</b>) Ranking of the importance of the characteristics of the influencing factors of the single-layer greenway (** refers to strong level feature importance; * Refers to the characteristic importance of medium and upper level strength); (<b>b</b>) Results of correlation fitting between WED and NI for the single-layer greenway.</p>
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<p>Perceptual maps of 2 features that have a significant effect on single-layer greenways.</p>
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<p>Map of feature perceptions that have a significant impact on double-layered greenways.</p>
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<p>Fitted plot of NI and GI correlation.</p>
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<p>Effect of changes in the height reduction of pavements on the BVI for a double-layered greenway.</p>
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<p>Model diagram of the single-layer greenway enhancement strategy. (<b>a</b>): Use of greenery to screen the urban environment. (<b>b</b>): Reducing the presence of railings. (<b>c</b>): Reduced height of fence enclosure. (<b>d</b>): Localised double-layered treatment of single-layer greenway.</p>
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<p>Model diagram of the double-layered greenway lift strategy. (<b>a</b>) Increase in event space, water-friendly space and stopping space. (<b>b</b>) Increase water perception for pedestrians through height changes. (<b>c</b>) Designs that can flood a greenway or space. (<b>d</b>) Partially designed as a submerged greenway. (<b>e</b>) Localised subsidence of embankment on the waterfront side.</p>
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15 pages, 5670 KiB  
Article
Changes in Wood Plastic Composite Properties After Natural Weathering and Potential Microplastic Formation
by Lotars O. Vasiljevs, Roze Zabarovska, Eva Gulevska, Dace Cirule, Errj Sansonetti, Ingeborga Andersone, Bruno Andersons, Janis Kajaks and Edgars Kuka
Forests 2024, 15(12), 2102; https://doi.org/10.3390/f15122102 - 27 Nov 2024
Viewed by 464
Abstract
Wood plastic composites (WPCs) have recently gained attention as alternatives to traditional wood materials for outdoor use, thanks to their enhanced moisture resistance and durability, which extends their service life. Discolouration as well as surface erosion has been observed during weathering for both [...] Read more.
Wood plastic composites (WPCs) have recently gained attention as alternatives to traditional wood materials for outdoor use, thanks to their enhanced moisture resistance and durability, which extends their service life. Discolouration as well as surface erosion has been observed during weathering for both WPCs with untreated and heat-treated wood. However, aspects such as changes in surface hydrophobicity, chemistry, and erosion in terms of microplastic formation have received less attention; this research aimed to evaluate these factors during natural weathering. Four types of WPC samples, consisting of 50% wood particles (untreated and heat-treated) and 50% polypropylene, were naturally weathered in Latvia for two years. The samples measured 240 mm × 240 mm × 5 mm. Results showed rapid colour changes, microcracks, and exposed wood particles, suggesting microplastic formation. ATR-FTIR analysis showed increased absorption at 1715 cm⁻¹ (carbonyl groups) and at 3410 cm−1 and 3460 cm−1, typical of wood, indicating chemical changes on the surface. These changes influenced surface hydrophobicity, roughness, and water penetration. In a relatively short exposure time, WPCs without proper additives undergo significant changes in their aesthetic and physical properties, leading to surface erosion and potential microplastic formation. This could challenge the perception of WPCs as environmentally friendly materials. Full article
(This article belongs to the Special Issue Wood Durability and Protection)
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<p>Experimental setup and scanning electron microscope image of unweathered surface.</p>
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<p>Average values of temperature, precipitation, humidity, and solar radiation each month from May 2022 until February 2024.</p>
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<p>Changes in surface colour of WPC samples: (<b>a</b>) South-facing side; (<b>b</b>) North-facing side. The bottom half of the sample was embedded in the ground and remained unexposed throughout the test—for this part, the colour changes were not evaluated.</p>
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<p>Changes in L*, a*, b* parameters for the surface of WPCs south-facing side: (<b>a</b>) Unweathered surface in comparison with 11 months of exposure to natural weathering; (<b>b</b>) Unweathered surface in comparison with 22 months of exposure to natural weathering.</p>
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<p>Changes in L*, a*, and b* parameters for the surface of WPCs north-facing side: (<b>a</b>) Unweathered surface in comparison with 11 months of exposure to natural weathering; (<b>b</b>) Unweathered surface in comparison with 22 months of exposure to natural weathering.</p>
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<p>ATR-FTIR spectra of wood and polypropylene unweathered and after 500 h of UV irradiation.</p>
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<p>ATR-FTIR spectra of WPC surface (unweathered and after 11 months of weathering the north-facing (N) and the south-facing side (S)).</p>
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<p>ATR-FTIR spectra of WPC surface (unweathered and after 22 months of weathering the north-facing (N) and the south-facing side (S)).</p>
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<p>Ra value for the surfaces of WPCs (unweathered and after 22 months of weathering north-facing (N) and the south-facing side (S)). <sup>1</sup> Groups with the same letters in the column indicate that there is no statistical difference (<span class="html-italic">p</span> &lt; 0.05) between exposure conditions within the sample series.</p>
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<p>K value for the surfaces of WPCs (unweathered and after 22 months of weathering the north-facing (N) and the south-facing side (S)). <sup>1</sup> Groups with the same letters in the column indicate that there is no statistical difference (<span class="html-italic">p</span> &lt; 0.05) between exposure conditions within the sample series.</p>
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<p>SEM images depicting the effects that natural weathering has on the surface of WPC.</p>
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13 pages, 2005 KiB  
Article
Effect of Thermovinification Temperature on Phenolic Compounds and Colour of Syrah Wine
by Islaine Santos Silva, Ana Paula André Barros, Luiz Claudio Correa, Carolina Oliveira de Souza and Aline Camarão Telles Biasoto
Beverages 2024, 10(4), 117; https://doi.org/10.3390/beverages10040117 - 27 Nov 2024
Viewed by 413
Abstract
Background: Thermovinification is a non-conventional winemaking practice that replaces the traditional method of grape maceration. Methods: This study evaluated the influence of thermovinification temperature on the quality of Syrah wines. The treatments included traditional winemaking with 7 days of maceration during alcoholic fermentation [...] Read more.
Background: Thermovinification is a non-conventional winemaking practice that replaces the traditional method of grape maceration. Methods: This study evaluated the influence of thermovinification temperature on the quality of Syrah wines. The treatments included traditional winemaking with 7 days of maceration during alcoholic fermentation at 23 °C (TW—control); and thermovinification for 2 h at 55 °C (TV55), 65 °C (TV65), and 75 °C (TV75). The red wines were made through microvinification (10-litre glass). Phenolic compounds (n = 26) were quantified by high-performance liquid chromatography and a colour analysis using the CIELab/CIEL*C*h systems and a sensory analysis was conducted to evaluate the acceptability of the thermovinified wine. Results: The results indicate that thermovinification increased the content of bioactive compounds and intensified the colour of the wine, reducing L* and a*. However, the content of phenolic acids decreased, except for trans-caftaric acid, which was approximately 50 times higher. A higher temperature of thermovinification (75 °C) promoted the degradation of all anthocyanins. Among flavonols, kaempferol-3-O-glucoside, quercetin-3-β-D-glucoside, and isorhamnetin-3-O-glucoside were higher in TV65 and TV75 wines. Greater amounts of stilbenes were quantified in TV65. Among the flavan-3-ols, TV75 stood out, especially for (+)-catechin, (−)-epicatechin, procyanidin A2, and procyanidin B1. Conclusions: The thermovinification at 65 °C is optimal for minimising anthocyanin degradation and improving Syrah wine quality. Full article
(This article belongs to the Section Wine, Spirits and Oenological Products)
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<p>Flowchart for production of Syrah red wines using traditional vinification and thermovinification.</p>
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<p>Total phenolic content measured using the Folin–Ciocalteu reducing capacity expressed in mg/L of gallic acid. Samples: TW, Syrah wine winemaking using traditional maceration; TV55, Syrah wine winemaking using thermovinification at 55 °C for 2 h; TV65, Syrah wine winemaking using thermovinification at 65 °C for 2 h; and TV75, Syrah wine winemaking using thermovinification at 75 °C for 2 h. Different letters indicate a significant difference between samples according to Tukey’s test (<span class="html-italic">p</span> ≤ 0.05).</p>
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<p>Colorimetric analysis (CIELAB and CIEL*C*h) of Syrah red wines elaborated at different thermovinification temperatures. Samples: TW, Traditional winemaking; TV55, Thermovinification at 55 °C; TV65, Thermovinification at 65 °C; and TV75, Thermovinification at 75 °C. Colour coordinates: L*, luminosity; a*, red/green component; b*, blue/yellow component; C*, saturation; and h, hue angle (h) Different letters indicate a significant difference between samples according to Tukey’s test (<span class="html-italic">p</span> ≤ 0.05).</p>
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<p>The principal component analysis (PCA) showing the configuration of Syrah wines vinified using different thermovinification temperatures, phenolic compounds (<span class="html-italic">n</span> = 26 compounds), and colour coordinates (L*, a*, b*, C*, and h). Samples: TW, Traditional winemaking; TV55, Thermovinification at 55 °C; TV65, Thermovinification at 65 °C; and TV75, Thermovinification at 75 °C.</p>
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<p>Data obtained from the sensory analysis of the Syrah thermovinified red wine at 65 °C. (<b>A</b>) The acceptance test conducted using a 9-point hybrid hedonic scale. (<b>B</b>) Results of the purchase intention test.</p>
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18 pages, 1772 KiB  
Article
The Demography, Longevity and Mortality of Bullmastiffs Attending Veterinary Practices in Australia
by Abigail Carney, Peter Williamson and Rosanne M. Taylor
Animals 2024, 14(23), 3419; https://doi.org/10.3390/ani14233419 - 26 Nov 2024
Viewed by 280
Abstract
The Bullmastiff is a giant breed of dog, and there is evidence the breed is predisposed to cancer and musculoskeletal disorders, though the disease investigation of the breed is limited. This study reports on the demography, longevity and mortality of Bullmastiffs attending veterinary [...] Read more.
The Bullmastiff is a giant breed of dog, and there is evidence the breed is predisposed to cancer and musculoskeletal disorders, though the disease investigation of the breed is limited. This study reports on the demography, longevity and mortality of Bullmastiffs attending veterinary practices in Australia over a ten-year period. VetCompass Australia collects patient data from veterinary practices across Australia for epidemiological analysis. All patient records of Bullmastiffs available in the VetCompass Australia database during this decade period were reviewed, with demographic information on the breed inclusive of coat colour, sex, neuter status, weight and location collated. Standardised veterinary diagnostic (VeNom) codes for the most appropriate cause of death were assigned to deceased dogs. The population comprised 2771 Bullmastiffs with an overall median age of 2.8 years. Within the group, 1259 were female (45.4%), 1491 were male (53.8%), and 21 dogs (0.8%) had no recorded sex or neuter status. Dogs grew rapidly in their first year, with an average gain of approximately 1 kg every 10 days. A slower growth rate continued in their second year, and growth plateaued as adulthood was reached, with the mean body weight of adult male dogs (46.6 kg) being heavier than that of females (40.5 kg). The age at death for the group was 8.5 years. The most common causes of death in the breed were mass lesions (28.2%), old age (9.9%), musculoskeletal-related disease (9.9%) and neurological (5.3%) and behavioural disorders (4.8%). Neutering was protective against mortality from urogenital causes (OR: 0.14; CI: 0.02–0.52; p = 0.003) and had a positive effect on longevity. This study provides demographic and health information on a population of Bullmastiffs attending veterinary practices in Australia, which will benefit evidence-based veterinary decisions for this breed. Additionally, the results may assist owners and breeders in making informed decisions on health risks and breeding programmes in the population. Full article
(This article belongs to the Section Companion Animals)
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<p>Number of births and deaths of Bullmastiffs attending veterinary care at practices participating in the VetCompass Australia programme from 1 January 2008 to 31 December 2017 compared to the number of Bullmastiffs registered with the ANKC for the corresponding years.</p>
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<p>Body weights and age for “well” male and female Bullmastiffs attending veterinary practices participating in the VetCompass Australia programme from 1 January 2008 to 31 December 2017 (males n = 970; females n = 777). Coloured lines indicate growth centiles.</p>
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<p>Body weights of young Bullmastiffs (&lt;24 months) attending veterinary care at practices participating in the VetCompass Australia programme from 1 January 2008 to 31 December 2017. The blue data points represent Bullmastiffs from 0 to 12 months, whilst the orange data points represent Bullmastiffs from 12 to 24 months.</p>
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15 pages, 556 KiB  
Article
Analysis of Water Activity and Gloss of Stored Goat Cheeses According to Consumer Preferences and Tastes
by Łukasz K. Kaczyński
Foods 2024, 13(23), 3789; https://doi.org/10.3390/foods13233789 - 25 Nov 2024
Viewed by 305
Abstract
Packaging is an integral part of every food product, especially cheese. An important goal is to protect the product from spoiling and drying out. Two types of cheese were tested: soft goat’s cheese and hard goat’s cheese. They were evaluated for gloss, water [...] Read more.
Packaging is an integral part of every food product, especially cheese. An important goal is to protect the product from spoiling and drying out. Two types of cheese were tested: soft goat’s cheese and hard goat’s cheese. They were evaluated for gloss, water activity, and colour. The aim of the research was to assess changes in the water activity of goat cheese in correlation with changes in gloss and color during storage in various forms of packaging, depending on consumer habits. The research problem was based on consumer observations regarding the repackaging of dairy products, including goat’s cheese. Consumers have reported such a problem in previous studies. The question was asked: will it be necessary in the future to indicate to the consumer the appropriate form of repackaging for a given goat’s cheese? It was shown that the best packaging for storing open feta-type goat salad cheeses was aluminum foil and hard goat cheeses in the producer’s packaging. The method of storage only affects the change in gloss in the case of goat salad cheese and parameter a* hard cheese. At the same time, the need was noted to develop appropriate packaging that would serve to protect the product from spoilage and would not pose a threat to the natural environment after being thrown into the trash. Wrapping soft goat cheeses in cellulose fiber paper reduced water activity by 5% after 14 days of storage but did not encourage re-consumption. The key task for future research is, therefore, to carry out regular consumer surveys. Therefore, it is necessary to choose (develop) a packaging that would preserve the original quality of the cheeses when stored in these conditions. Full article
(This article belongs to the Section Sensory and Consumer Sciences)
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<p>Translational movement of water in soft goat cheese and hard goat cheese. aw<sub>m</sub> = mean water activity translation area; Δτ = duration of translational water movement in minutes; aw<sub>s</sub> = initial water activity; aw<sub>E</sub> = final water activity.</p>
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16 pages, 1067 KiB  
Article
Alcoholic Fermentation Activators: Bee Pollen Extracts as a New Alternative
by Juan Manuel Pérez-González, José Manuel Igartuburu, Víctor Palacios, Pau Sancho-Galán, Ana Jiménez-Cantizano and Antonio Amores-Arrocha
Agronomy 2024, 14(12), 2802; https://doi.org/10.3390/agronomy14122802 - 25 Nov 2024
Viewed by 381
Abstract
Searching for natural alternatives to synthetic fermentation activators has led to the study of bee pollen as a natural alcoholic fermentation activator. This study evaluated the potential of different bee pollen extracts (0.25 g/L) as activators in a Palomino Fino grape must. By [...] Read more.
Searching for natural alternatives to synthetic fermentation activators has led to the study of bee pollen as a natural alcoholic fermentation activator. This study evaluated the potential of different bee pollen extracts (0.25 g/L) as activators in a Palomino Fino grape must. By analysing the composition of each extract, it was possible to identify the specific bee pollen fractions with the highest efficacy for activating alcoholic fermentation. Four extracts were obtained through sequential extraction using various organic solvents of increasing polarity (hexane, acetone, ethanol, and water), and their compositions were characterised. The effect of each extract was evaluated by monitoring the viable yeast populations and fermentation kinetics throughout the alcoholic fermentation process, along with the physicochemical and colour characterisation of the white wines obtained. The bee pollen fraction extracted with hexane, which was rich in long-chain fatty acids, significantly increased the maximum yeast populations and improved the fermentation kinetics. However, the extracts rich in polyphenolic compounds exhibited slower fermentation rates. Based on the obtained results, the lipid fraction of bee pollen extracted with hexane may be responsible for its ability to activate alcoholic fermentation. Full article
(This article belongs to the Special Issue Extraction and Analysis of Bioactive Compounds in Crops—2nd Edition)
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<p>Development of viable <span class="html-italic">Saccharomyces cerevisiae</span> during the process of alcoholic fermentation of the Palomino Fino grape must using bee pollen extracts, bee pollen, or a control.</p>
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<p>Relative density evolution during alcoholic fermentation of Palomino Fino grape must using doses of bee pollen and extracts.</p>
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<p>Evolution of YAN in Palomino Fino grape must using doses of bee pollen extracts, bee pollen, and control during alcoholic fermentation.</p>
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<p>Olfactory and taste evaluation of Palomino Fino wines made with bee pollen or bee pollen extracts and control. Stars (*) indicate significant differences between trials for the respective attributes (ANOVA, <span class="html-italic">p</span> &lt; 0.05), as determined by a two-way ANOVA and applying a Bonferroni multiple range (BSD) test.</p>
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