Multispectral Imaging for Quality Determinations of White Meat: Comparison
Please note this is a comparison between Version 2 by Peter Tang and Version 1 by Wen-Hao Su.

White meat is the nutritional term for lighter-colored meat that contains less myoglobin than red meat, which contains a great deal. White meat includes poultry (e.g., chicken, duck, goose and turkey), fish, reptiles (e.g., land snail), amphibians (e.g., frog), crustaceans (e.g., shrimp and crab) and bivalves (e.g., oyster and clam), but it excludes all mammal flesh such as beef, pork, and lamb. White meat has high nutritional value and plays an important role in human diet. The production and sale of white meat need to meet specific quality and safety standards. Fluorescence spectroscopy, color imaging and multispectral imaging (MSI) have emerged as effective analytical methods for the non-destructive detection of quality attributes of various white meat products such as fish, shrimp, chicken, duck and goose.

  • white meat
  • multispectral imaging
  • fluorescence spectroscopy
  • convolutional neural network
  • quality detection

1. Introduction

As a global issue, food safety and quality are of increasing concern to companies and customers [1]. White meat is the nutritional term for lighter-colored meat that contains less myoglobin than red meat, which contains a great deal. Compared with white meat, the intake of red meat has a greater correlation with colorectal cancer (CRC), indicating that white meat intake is more beneficial to human health [2]. White meat includes poultry (e.g., chicken, duck, goose and turkey), fish, reptiles (e.g., land snail), amphibians (e.g., frog), crustaceans (e.g., shrimp and crab) and bivalves (e.g., oyster and clam), but it excludes all mammal flesh such as beef, pork, and lamb. White meat has high nutritional value and plays an important role in human diet. The production and sale of white meat need to meet specific quality and safety standards. The freshness of fish is one of the important indicators for evaluating its quality because of its high perishability [3]. Moreover, poultry products are particularly susceptible to oxidation as this meat contains relatively high levels of unsaturated fatty acids and low levels of natural antioxidants, such as vitamin E. In addition, chemical residues in white meat may have an adverse effect on human health. For example, fluoroquinolone antibiotics are effective against a wide range of Gram-negative and positive bacteria, thus they are widely used in the medical and veterinary fields. However, their use in animals has raised concerns, as this practice may lead to an increase in microbial resistance [4]. Moreover, nitrofuran drugs (NFs), including furazolidone (FZD), nitrofurazone (NFZ), and furantazone (FTD) are broad-spectrum antimicrobials. The potential risk of these compounds to human health is of great concern because of their carcinogenic and mutagenic properties. It is therefore crucial to ensure the quality and safety of white meat.
Traditional methods for meat quality and safety evaluation, such as manual inspection, mechanical and chemical methods, are time-consuming and destructive, and cannot meet the requirements of rapid inspection [5]. For example, methods for freshness evaluation are based on human sensory qualities, such as appearance, taste and texture. However, human senses exhibit a very high degree of subjectivity and can therefore be questioned in certain situations [3]. Even if manual inspection could meet accuracy requirements, it is still a labor-intensive and time-consuming process. Recently, the meat industry has adopted the most advanced high-speed processing technologies, and meat processors need fast, non-destructive, easy-to-use techniques to control the safety and quality of meat and meat products in order to achieve economic benefits. The requirement for real-time monitoring of food has encouraged the development of non-destructive measurement systems [6]. Optical technology is becoming increasingly important in research and industrial applications to measure the quality attributes of meat and meat products in real time, non-destructively and accurately [7]. Among these, the use of neural network-based RGB imaging technology has become very popular in recent years [8]. In addition, fluorescence spectroscopy and multispectral imaging (MSI) also show obvious advantages and capabilities in the non-destructive evaluation of white meat.
There have been several reviews of these new techniques of meat quality assessment. These papers show that these spectroscopic methods have been implemented as an alternative to traditional methods, but they mainly focus on one technique for quality detection of one specific category of meat, e.g., fish [3], shrimp [4], chicken [9], duck [10], or red meat [11]. As far as wthe researchers know, there is no literature review analyzing the application of various imaging techniques in the non-destructive quality inspection of various white meats. (The published reviews based on these three imaging techniques are tabulated in Table 1).
Table 1. Summary of reviews on fluorescence spectroscopy, RGB- and MSI techniques in food evaluation.
 

Technology

Product

Target Attributes

Reference

MSI

Meat

Adulteration

Ropodi et al. [12]

MSI, HSI

Meat

Defects

Feng et al. [13]

MSI

Food

Quality

Su and Sun

[35]. Data obtained from pure RGB imaging has been shown to be inferior to data obtained through spectral imaging when analyzing the quality of ground meat.
Figure 2.
Diagram of the RGB vision system used to obtain color images of pure and contaminated meat samples [33].
A multispectral image is a collection of grey-scale images. Each corresponds to a specific wavelength or band of wavelengths in the electromagnetic spectrum [36]. MSI is a method of capturing images from different spectral bands with the aim of obtaining spatial and spectral information. Imagers based on MSI technology can provide wavelength channels in the near-UV, visible, near-IR, mid-IR and far-IR [37]. Thus, MSI can provide more information than RGB images. The acquired wavelength channels can be used directly for real-time applications in certain fields (e.g., fruit packing plants and food processing plants). A typical MSI system is shown in Figure 3. The system uses an adjustable focus lens to achieve high resolution imaging of 1290 × 960 pixels and has six bands, each covering a relatively wide range of wavelengths, which is strong for fast imaging [38].
Figure 3. The MSI system consists of a light source (HL-2000-FHSA; Ocean Optics, Dunedin, FL, USA) and focusable lens (Nikon, Tokyo, Japan) plus a multi-channel spectral camera (miniCAM5; QHY-CCD, China) [38].

3. Quality Evaluation of White Meat

The application of fluorescence spectroscopy, RGB imaging and MSI for white meat quality inspection has been thoroughly and extensively researched as shown in Table 2.  For MSI techniques, correlation coefficient (R) or coefficient of determination (R2) is an important statistical metric for assessing model fit, while root mean square error (RMSE) is considered an indicator of the sample standard deviation between measured and actual values, indicating that a well-performing model should obtain a high R or R2 value and a low RMSE value. There are many different judgements due to the variability and multiplicity of the techniques.
Table 2. Applications of fluorescence spectroscopy, RGB imaging and MSI for quality evaluation of various white meat products.

White Meat

Module

Quality Parameters

Accuracy

Reference

Fish

MSI

TVB-N,

PPC

R2p = 0.862 for TVB-N,

R2p = 0.921 for PPC

Khoshnoudi-Nia and Moosavi-Nasab [39], Khoshnoudi-Nia and Moosavi-Nasab [40]

Fish

MSI

TVC

R2 = 0.62

Govari, et al. [41]

[

14

]

Fish

MSI

TVC

R2 = 0.683

Fengou, et al. [42]

MSI, IRS, SERS, LIBS and HSI

Fish

Food

MSI

Quality

Astaxanthin concentration

Wang et al. [15]

R

2

= 0.86

Dissing, et al. [43]

MSI, HSI and VS

Food

Fish

MSI

Authenticity, quality and safety

TVB-N,

TBARS,

K

Ropodi et al. [16]

R

2

p = 0.922 for TVB-N,

R2p = 0.867 for TBARS,

R2p = 0.936 for K

Cheng, et al. [44]

Fluorescence spectroscopy

Fish

Food

Quality

MSI

Karoui and Blecker [

A ‘standard freshness index’ of K

17]

R

2

= 0.94,

Omwange, et al. [45]

Fluorescence spectroscopy

Food

Fish

Fluorescence spectroscopy

Quality

A ‘standard freshness index’ of K

Strasburg and Ludescher [18]

R

2

= 0.92

Omwange, et al. [46]

Visible/Infrared, Raman and Fluorescence spectroscopy

Fish

Raw and processed food

Fluorescence spectroscopy

Quality

A ‘standard freshness index’ of K

He and Sun [19]

R

2

= 0.95

Liao, et al. [47]

Fluorescence spectroscopy

Food

Quality

Fish

Fluorescence spectroscopy

Ahmad et al. [20]

AEC;

NADH

R2 = 0.90 for AEC,

R2 = 0.85 for NADH

Rahman, et al. [

Fluorescence spectroscopy

Dairy products

Quality and safety

Shaikh and O’Donnell [21]

48

]

Fish

Fluorescence spectroscopy

NADH

90.5%

Hassoun and Karoui [49]

Fluorescence spectroscopy

Fresh and frozen-thawed muscle foods

Muscle classification

Fish

RGB imaging

Classification performance

Hassoun [22]

99.5%

Park, et al. [50]

RGB-Imaging

Fish

Meat

RGB imaging

Quality and safety

Astaxanthin concentration

Taheri-Garavand et al. [23]

R

2

= 0.66

Dissing et al. [43

RGB-Imaging

Fish

Quality

Dowlati et al. [24]

RGB-Imaging

Food

Quality

Gomes and Leta [25]

RGB-Imaging

Food

Quality

Amani et al. [26]

MSI––Multispectral imaging; HSI––Hyperspectral imaging; IRS––Infrared spectroscopy; SERS––Surface-Enhanced Raman Spectroscopy; LIBS––Laser induced breakdown spectroscopy; VS––Vibrational Spectroscopy.

2. Fluorescence Spectroscopy, RGB- and Multispectral-Imaging

Fluorescence spectroscopy has proven to be an effective analytical technique over the last decade for monitoring the properties of various food products [27]. The number of published papers and citations on the use of fluorescence spectroscopy to study food quality and/or authenticity has increased exponentially over the last decade. Fluorescence is the emission of light by a fluorophore following the absorption of ultraviolet or visible light [28]. Fluorophores absorb energy as light at specific wavelengths and release energy as light at higher wavelengths. The Jablonski diagram in Figure 1 illustrates the electron energy levels of fluorophores, with the jumps between them indicated by arrows [29]. Fluorescent compounds are highly sensitive to their environment, so fluorescence can be used to characterize the conformational changes that occur under different production and storage conditions [21]. For specific applications, fluorescence analysis has the lowest background levels, low detection limits and is readily available in most laboratories [30].
Figure 1.
Jablonski diagram of the electron energy levels and transitions of fluorophores [29].
RGB imaging or color imaging has gained popularity due to its clear color rendering principle, simple hardware structure and mature production process. RGB images are captured by digital cameras, webcams, or scanners from computer vision systems. These systems, typically containing an illumination system, camera and image analysis software using a computer [31], are capable of retrieving color information from captured images in the form of pixel ribbons of RGB [32]. Figure 2, for example, shows an RGB vision system for capturing color images of pure and adulterated meat samples [33]. RGB imaging has been shown to determine the general color and visual appearance of samples [34]. This imaging technology is valuable in the meat industry because it is simple, low cost and non-destructive. However, even though RGB imaging has many advantages, it only provides spatial information at a limited number of wavelengths. Conventional RGB imaging systems can be poor at identifying sensitive surface features in wavelengths other than RGB

]

Fish

RGB imaging

Freshness of tuna meat cuts

86.67%

Lugatiman, et al. [51]

Fish

RGB imaging

The main color of the sample

75%

Mateo, et al. [52]

Fish

RGB imaging

Texture features

86.3%

Gu, et al. [53]

Fish

RGB imaging

Color of Salmon Fillets

R = 0.95

Quevedo, et al. [54]

Fish

RGB imaging

Gill and eye color changes in the sparus aurata

R2 = 0.994

Dowlati, et al. [55]

Fish

RGB imaging

Body color of carp

94.97%

Taheri-Garavand, et al. [56]

Fish

RGB imaging

Freshness

98.2%

Rocculi, et al. [57]

Shrimp

Fluorescence spectroscopy

4-hexylresorcinol

81.6%

Jonker and Dekker [58]

Shrimp

Fluorescence spectroscopy

K, pH

R2 = 0.80

Rahman, et al. [59]

Shrimp

RGB imaging

pH

100%

Witjaksono, et al. [60]

Shrimp

RGB imaging

Identification accuracy of the proposed ShrimpNet for shrimp

95.48%

Hu, et al. [61]

Shrimp

RGB imaging

Shrimp dehydration levels

R = 0.86

Mohebbi, et al. [62]

Shrimp

RGB imaging

Color changes in the head, legs and tail of pacific white shrimp (litopenaeus vannamei)

90%

Ghasemi-Varnamkhasti, et al. [63]

Chicken

Fluorescence spectroscopy

Hydroxyproline concentration

R2 = 0.82

Monago-Maraña, et al. [64]

Chicken

MSI

Skin tumors

86%

Chao, et al. [65]

Chicken

MSI

TVC

90.4%

Spyrelli, et al. [66]

Chicken

MSI

pork-chicken adulteration

90.00% for fresh samples, 86.67% for frozen-thawed samples

Fengou, et al. [67]

Chicken

MSI

Sepsis in chickens

98.6% for septic chickens,

96.3% for healthy chickens

Yang, et al. [68]

Chicken

MSI

Contamination detection

96%

Park, et al. [69]

Chicken

MSI

Chicken heart disease characterization

100%

Chao, et al. [70]

Chicken

MSI;

Fluorescence spectroscopy

Contamination detection

92.5%

Seo, et al. [71]

Chicken

Fluorescence spectroscopy

Lipid oxidation

R = 0.73

Gatellier, et al. [72]

Chicken

Fluorescence spectroscopy

P. aeruginosa concentration

96%

Abdel-Salam, et al. [73]

Chicken

Fluorescence spectroscopy

chicken meat tenderness

R = 0.870

Yu, et al. [74]

Chicken

Fluorescence spectroscopy

Contamination detection

96.6%

Cho, et al. [75]

Chicken

Fluorescence spectroscopy

Measurement of lipid oxidation

98%

Wold and Kvaal [76]

Chicken

RGB imaging

Avian flu infected chickens

97.43%

Cuan, et al. [77]

Chicken

RGB im-aging

Color

94%

Yumono, et al. [78]

Chicken

RGB im-aging

Freshness

R = 0.987

Taheri-Garavand, et al. [79]

Duck

Fluorescence spectroscopy

Gentamicin Residual in Duck Meat

R = 0.996

Wang, et al. [80]

Duck

Fluorescence spectroscopy

Doxycycline content in duck meat

R = 0.998

Wang, et al. [81]

Duck

Fluorescence spectroscopy

Carbaryl residue in duck meat

R = 0.976

Xiao et al. [10]

Duck

Fluorescence spectroscopy

Tetracycline content

R = 0.952

Zhao, et al. [82]

Duck

Fluorescence spectroscopy

Triazophos content

R2p =  0.974,

Zhao, et al. [83]

Duck

Fluorescence spectroscopy

Neomycin residue

R = 0.999

Jiang, et al. [84]

Duck

Fluorescence spectroscopy

Carbofuran residue

R2p =  0.999

XIAO, et al. [85]

TVB-N––total volatile basic nitrogen; PPC—Psycho-trophic Plate Count; TVC—total viable count; LDA—Linear Discriminant Analysis; MD—Mahalanobis distance; PCA—Principal component analysis; m—mean; TBARS—Thio-barbituric acid reactive substances; AEC—adenylate energy charge; NAD and NADH—nicotinamide adenine dinucleotide; CFU—colony-forming units; TBARS—thio-barbituric acid reactive substances.

References

  1. Xiong, Z.; Xie, A.; Sun, D.-W.; Zeng, X.-A.; Liu, D. Applications of Hyperspectral Imaging in Chicken Meat Safety and Quality Detection and Evaluation: A Review. Crit. Rev. Food Sci. Nutr. 2014, 55, 1287–1301.
  2. Aykan, N.F. Red meat subtypes and colorectal cancer risk. Int. J. Cancer 2015, 137, 1788.
  3. Tsagkatakis, G.; Nikolidakis, S.; Petra, E.; Kapantagakis, A.; Grigorakis, K.; Katselis, G.; Vlahos, N.; Tsakalides, P.J.E.I. Fish Freshness Estimation though analysis of Multispectral Images with Convolutional Neural Networks. IST Int. Symp. Electron. Imaging 2020, 2020, 171.
  4. Schneider, M.J.; Vazquez-Moreno, L.; Bermudez-Almada, M.D.C.; Guardado, R.B.; Ortega-Nieblas, M.J.J.O.A.I. Multiresidue Determination of Fluoroquinolones in Shrimp by Liquid Chromatography-Fluorescence-Mass Spectrometryn. J. AOAC Int. 2005, 88, 1160–1166.
  5. Xiong, Z.; Sun, D.-W.; Pu, H.; Gao, W.; Dai, Q. Applications of emerging imaging techniques for meat quality and safety detection and evaluation: A review. Crit. Rev. Food Sci. Nutr. 2017, 57, 755–768.
  6. Kamruzzaman, M.; Makino, Y.; Oshita, S. Non-invasive analytical technology for the detection of contamination, adulteration, and authenticity of meat, poultry, and fish: A review. Anal. Chim. Acta 2015, 853, 19–29.
  7. Peng, Y.; Dhakal, S. Optical Methods and Techniques for Meat Quality Inspection. Trans. ASABE 2015, 58, 1371–1386.
  8. Qin, J.; Kim, M.S.; Chao, K.; Dhakal, S.; Lee, H.; Cho, B.-K.; Mo, C. Detection and quantification of adulterants in milk powder using a high-throughput Raman chemical imaging technique. Food Addit. Contam. Part A 2017, 34, 152–161.
  9. Yang, C.-C.; Chao, K.; Chen, Y.-R. Development of multispectral image processing algorithms for identification of wholesome, septicemic, and inflammatory process chickens. J. Food Eng. 2005, 69, 225–234.
  10. Xiao, H.-B.; Liu, M.-H.; Yuan, H.-C.; Xu, J.; Zhao, J.-H. Study on determination of carbaryl content in duck meat based on synchronous fluorescence spectroscopy. Spectrosc. Spectr. Anal. 2012, 32, 3058–3062.
  11. Wang, W.; Peng, Y.; Sun, H.; Zheng, X.; Wei, W. Spectral Detection Techniques for Non-Destructively Monitoring the Quality, Safety, and Classification of Fresh Red Meat. Food Anal. Methods 2018, 11, 2707–2730.
  12. Ropodi, A.I.; Panagou, E.Z.; Nychas, G.-J.E. Multispectral imaging (MSI): A promising method for the detection of minced beef adulteration with horsemeat. Food Control 2017, 73, 57–63.
  13. Feng, C.-H.; Makino, Y.; Oshita, S.; Martín, J.F.G. Hyperspectral imaging and multispectral imaging as the novel techniques for detecting defects in raw and processed meat products: Current state-of-the-art research advances. Food Control 2018, 84, 165–176.
  14. Su, W.-H.; Sun, D.-W. Multispectral Imaging for Plant Food Quality Analysis and Visualization. Compr. Rev. Food Sci. Food Saf. 2018, 17, 220–239.
  15. Wang, K.; Pu, H.; Sun, D.-W. Emerging Spectroscopic and Spectral Imaging Techniques for the Rapid Detection of Microorganisms: An Overview. Compr. Rev. Food Sci. Food Saf. 2018, 17, 256–273.
  16. Ropodi, A.; Panagou, E.; Nychas, G.-J. Data mining derived from food analyses using non-invasive/non-destructive analytical techniques; determination of food authenticity, quality & safety in tandem with computer science disciplines. Trends Food Sci. Technol. 2016, 50, 11–25.
  17. Karoui, R.; Blecker, C. Fluorescence Spectroscopy Measurement for Quality Assessment of Food Systems—A Review. Food Bioprocess Technol. 2011, 4, 364–386.
  18. Strasburg, G.M.; Ludescher, R. Theory and applications of fluorescence spectroscopy in food research. Trends Food Sci. Technol. 1995, 6, 69–75.
  19. He, H.-J.; Sun, D.-W. Microbial evaluation of raw and processed food products by Visible/Infrared, Raman and Fluorescence spectroscopy. Trends Food Sci. Technol. 2015, 46, 199–210.
  20. Ahmad, M.H.; Sahar, A.; Hitzmann, B. Fluorescence Spectroscopy for the Monitoring of Food Processes. Meas. Modeling Autom. Adv. Food Processing 2017, 161, 121–151.
  21. Shaikh, S.; O’Donnell, C. Applications of fluorescence spectroscopy in dairy processing: A review. Curr. Opin. Food Sci. 2017, 17, 16–24.
  22. Hassoun, A. Exploring the Potential of Fluorescence Spectroscopy for the Discrimination between Fresh and Frozen-Thawed Muscle Foods. Photochem 2021, 1, 247–263.
  23. Taheri-Garavand, A.; Fatahi, S.; Omid, M.; Makino, Y. Meat quality evaluation based on computer vision technique: A review. Meat Sci. 2019, 156, 183–195.
  24. Dowlati, M.; de la Guardia, M.; Mohtasebi, S.S. Application of machine-vision techniques to fish-quality assessment. TrAC Trends Anal. Chem. 2012, 40, 168–179.
  25. Gomes, J.F.S.; Leta, F.R. Applications of computer vision techniques in the agriculture and food industry: A review. Eur. Food Res. Technol. 2012, 235, 989–1000.
  26. Amani, H.; Badak-Kerti, K.; Khaneghah, A.M. Current progress in the utilization of smartphone-based imaging for quality assessment of food products: A review. Crit. Rev. Food Sci. Nutr. 2020, 1–13.
  27. Dufour, E.; Frencia, J.P.; Kane, E. Development of a rapid method based on front-face fluorescence spectroscopy for the monitoring of fish freshness. Food Res. Int. 2003, 36, 415–423.
  28. Hassoun, A.; Sahar, A.; Lakhal, L.; Aït-Kaddour, A. Fluorescence spectroscopy as a rapid and non-destructive method for monitoring quality and authenticity of fish and meat products: Impact of different preservation conditions. LWT 2019, 103, 279–292.
  29. Yokota, H.; Fukasawa, A.; Hirano, M.; Ide, T. Low-Light Photodetectors for Fluorescence Microscopy. Appl. Sci. 2021, 11, 2773.
  30. Karbiwnyk, C.M.; Carr, L.E.; Turnipseed, S.B.; Andersen, W.C.; Miller, K.E. Determination of quinolone residues in shrimp using liquid chromatography with fluorescence detection and residue confirmation by mass spectrometry. Anal. Chim. Acta 2007, 596, 257–263.
  31. Liu, Z.; Zhong, Y.; Hu, Y.; Yuan, L.; Luo, R.; Chen, D.; Wu, M.; Huang, H.; Li, Y. Fluorescence strategy for sensitive detection of adenosine triphosphate in terms of evaluating meat freshness. Food Chem. 2019, 270, 573–578.
  32. Mohd Ali, M.; Hashim, N.; Khairunniza-Bejo, S.; Shamsudin, R.; Wan Sembak, W. RGB imaging system for monitoring quality changes of seedless watermelon during storage. In Proceedings of the III International Conference on Agricultural and Food Engineering 1152, Kuala Lumpur, Malaysia, 13 May 2016; pp. 361–366.
  33. Rady, A.M.; Adedeji, A.; Watson, N.J.J.J.O.A.; Research, F. Feasibility of utilizing color imaging and machine learning for adulteration detection in minced meat. J. Agric. Food Res. 2021, 6, 100251.
  34. Barbin, D.F.; Mastelini, S.M.; Barbon, S.; Campos, G.F.C.; Barbon, A.P.A.C.; Shimokomaki, M. Digital image analyses as an alternative tool for chicken quality assessment. Biosyst. Eng. 2016, 144, 85–93.
  35. Taghizadeh, M.; Gowen, A.A.; O’Donnell, C.P. Comparison of hyperspectral imaging with conventional RGB imaging for quality evaluation of Agaricus bisporus mushrooms. Biosyst. Eng. 2011, 108, 191–194.
  36. Bandara, W.; Prabhath, G.; Dissanayake, D.; Herath, H.; Godaliyadda, G.; Ekanayake, M.; Vithana, S.; Demini, S.; Madhujith, T. A multispectral imaging system to assess meat quality. In Proceedings of the 2018 IEEE Region 10 Humanitarian Technology Conference (R10-HTC), Malambe, Sri Lanka, 6–8 December 2018; pp. 1–6.
  37. Jayasundara, D.; Ramanayake, L.; Senarath, N.; Herath, S.; Godaliyadda, R.; Ekanayake, P.; Herath, V.; Ariyawansha, S. Multispectral Imaging for Automated Fish Quality Grading. In Proceedings of the 2020 IEEE 15th International Conference on Industrial and Information Systems (ICIIS), Rupnagar, India, 26–28 November 2020; pp. 321–326.
  38. Li, A.; Li, C.; Gao, M.; Yang, S.; Liu, R.; Chen, W.; Xu, K. Beef Cut Classification Using Multispectral Imaging and Machine Learning Method. Front. Nutr. 2021, 8.
  39. Khoshnoudi-Nia, S.; Moosavi-Nasab, M. Prediction of various freshness indicators in fish fillets by one multispectral imaging system. Sci. Rep. 2019, 9, 14704.
  40. Khoshnoudi-Nia, S.; Moosavi-Nasab, M. Nondestructive Determination of Microbial, Biochemical, and Chemical Changes in Rainbow Trout (Oncorhynchus mykiss) During Refrigerated Storage Using Hyperspectral Imaging Technique. Food Anal. Methods 2019, 12, 1635–1647.
  41. Govari, M.; Tryfinopoulou, P.; Parlapani, F.; Boziaris, I.S.; Panagou, E.Z.; Nychas, G.-J. Quest of Intelligent Research Tools for Rapid Evaluation of Fish Quality: FTIR Spectroscopy and Multispectral Imaging Versus Microbiological Analysis. Foods 2021, 10, 264.
  42. Fengou, L.-C.; Lianou, A.; Tsakanikas, P.; Gkana, E.N.; Panagou, E.Z.; Nychas, G.-J.E. Evaluation of Fourier transform infrared spectroscopy and multispectral imaging as means of estimating the microbiological spoilage of farmed sea bream. Food Microbiol. 2019, 79, 27–34.
  43. Dissing, B.S.; Nielsen, M.C.E.; Ersbøll, B.K.; Frosch, S. Multispectral Imaging for Determination of Astaxanthin Concentration in Salmonids. PLoS ONE 2011, 6, e19032.
  44. Cheng, J.-H.; Sun, D.-W.; Qu, J.-H.; Pu, H.-B.; Zhang, X.-C.; Song, Z.; Chen, X.; Zhang, H. Developing a multispectral imaging for simultaneous prediction of freshness indicators during chemical spoilage of grass carp fish fillet. J. Food Eng. 2016, 182, 9–17.
  45. Omwange, K.A.; Saito, Y.; Zichen, H.; Khaliduzzaman, A.; Kuramoto, M.; Ogawa, Y.; Kondo, N.; Suzuki, T. Evaluating Japanese dace (Tribolodon hakonensis) fish freshness during storage using multispectral images from visible and UV excited fluorescence. LWT 2021, 151, 112207.
  46. Omwange, K.A.; Al Riza, D.F.; Sen, N.; Shiigi, T.; Kuramoto, M.; Ogawa, Y.; Kondo, N.; Suzuki, T. Fish freshness monitoring using UV-fluorescence imaging on Japanese dace (Tribolodon hakonensis) fisheye. J. Food Eng. 2020, 287, 110111.
  47. Liao, Q.H.; Suzuki, T.; Yasushi, K.; Al Riza, D.F.; Kuramoto, M.; Kondo, N. Monitoring Red Sea Bream Scale Fluorescence as a Freshness Indicator. Fishes 2017, 2, 10.
  48. Rahman, M.M.; Shibata, M.; ElMasry, G.; Nakazawa, N.; Nakauchi, S.; Hagiwara, T.; Osako, K.; Okazaki, E. Expeditious prediction of post-mortem changes in frozen fish meat using three-dimensional fluorescence fingerprints. Biosci. Biotechnol. Biochem. 2019, 83, 901–913.
  49. Hassoun, A.; Karoui, R. Front-face fluorescence spectroscopy coupled with chemometric tools for monitoring fish freshness stored under different refrigerated conditions. Food Control 2015, 54, 240–249.
  50. Park, J.-H.; Hwang, K.-B.; Park, H.-M.; Choi, Y.-K.J.J.O.T.K.I.O.I.; Engineering, C. Application of CNN for fish species classification. J. Korea Inst. Inf. Commun. Eng. 2019, 23, 39–46.
  51. Lugatiman, K.; Fabiana, C.; Echavia, J.; Adtoon, J.J. Tuna Meat Freshness Classification through Computer Vision. In Proceedings of the 2019 IEEE 11th International Conference on Humanoid, Nanotechnology, Information Technology, Communication and Control, Environment, and Management (HNICEM), Laoag, Philippines, 29 November–1 December 2019; pp. 1–6.
  52. Mateo-Aroca, A.; Soto, F.; Villarejo, J.A.; Roca-Dorda, J.; De La Gándara, F.; García, A. Quality analysis of tuna meat using an automated color inspection system. Aquac. Eng. 2006, 35, 1–13.
  53. Gu, J.; He, N.; Wu, X. A new detection method for fish freshness. In Proceedings of the 2014 Seventh International Symposium on Computational Intelligence and Design, Hangzhou, China, 13–14 December 2014; pp. 555–558.
  54. Quevedo, R.A.; Aguilera, J.M.; Pedreschi, F. Color of Salmon Fillets By Computer Vision and Sensory Panel. Food Bioprocess Technol. 2008, 3, 637–643.
  55. Dowlati, M.; Mohtasebi, S.S.; Omid, M.; Razavi, S.H.; Jamzad, M.; de la Guardia, M. Freshness assessment of gilthead sea bream (Sparus aurata) by machine vision based on gill and eye color changes. J. Food Eng. 2013, 119, 277–287.
  56. Taheri-Garavand, A.; Fatahi, S.; Banan, A.; Makino, Y. Real-time nondestructive monitoring of Common Carp Fish freshness using robust vision-based intelligent modeling approaches. Comput. Electron. Agric. 2019, 159, 16–27.
  57. Rocculi, P.; Cevoli, C.; Tappi, S.; Genovese, J.; Urbinati, E.; Picone, G.; Fabbri, A.; Capozzi, F.; Dalla Rosa, M. Freshness assessment of European hake (Merluccius merluccius) through the evaluation of eye chromatic and morphological characteristics. Food Res. Int. 2019, 115, 234–240.
  58. Jonker, K.M.; Dekker, C.P. Determination of 4-Hexylresorcinol in Shrimp by Liquid Chromatography with Fluorescence Detection. J. AOAC Int. 2000, 83, 241–244.
  59. Rahman, M.; Bui, M.V.; Shibata, M.; Nakazawa, N.; Rithu, M.N.A.; Yamashita, H.; Sadayasu, K.; Tsuchiyama, K.; Nakauchi, S.; Hagiwara, T.; et al. Rapid noninvasive monitoring of freshness variation in frozen shrimp using multidimensional fluorescence imaging coupled with chemometrics. Talanta 2021, 224, 121871.
  60. Witjaksono, G.; Hussin, N.H.F.B.M.; Rabih, A.A.S.; Alfa, S. Real time chromametry measurement for food quality detection using mobile device. In Proceedings of the IOP Conference Series: Materials Science and Engineering, Busan, Korea, 25–27 August 2017; p. 12024.
  61. Hu, W.-C.; Wu, H.-T.; Zhang, Y.-F.; Zhang, S.-H.; Lo, C.-H. Shrimp recognition using ShrimpNet based on convolutional neural network. J. Ambient. Intell. Humaniz. Comput. 2020, 1–8.
  62. Mohebbi, M.; Akbarzadeh-T, M.-R.; Shahidi, F.; Moussavi, M.; Ghoddusi, H.-B. Computer vision systems (CVS) for moisture content estimation in dehydrated shrimp. Comput. Electron. Agric. 2009, 69, 128–134.
  63. Ghasemi-Varnamkhasti, M.; Goli, R.; Forina, M.; Mohtasebi, S.S.; Shafiee, S.; Naderi-Boldaji, M. Application of Image Analysis Combined with Computational Expert Approaches for Shrimp Freshness Evaluation. Int. J. Food Prop. 2016, 19, 2202–2222.
  64. Monago-Maraña, O.; Wold, J.P.; Rødbotten, R.; Dankel, K.R.; Afseth, N.K. Raman, near-infrared and fluorescence spectroscopy for determination of collagen content in ground meat and poultry by-products. LWT 2021, 140, 110592.
  65. Chao, K.; Mehl, P.M.; Kim, M.S.; Chen, Y.-R. Detection of chicken skin tumors by mutlispectral imaging. In Proceedings of the Photonic Detection and Intervention Technologies for Safe Food, Bellingham, WA, USA, 5–6 November 2000; pp. 214–223.
  66. Spyrelli, E.D.; Ozcan, O.; Mohareb, F.; Panagou, E.Z.; Nychas, G.J.E. Spoilage assessment of chicken breast fillets by means of fourier transform infrared spectroscopy and multispectral image analysis. Curr. Res. Food Sci. 2021, 4, 121–131.
  67. Fengou, L.-C.; Lianou, A.; Tsakanikas, P.; Mohareb, F.; Nychas, G.-J.E. Detection of Meat Adulteration Using Spectroscopy-Based Sensors. Foods 2021, 10, 861.
  68. Yang, C.-C.; Chao, K.; Chen, Y.-R.; Kim, M.S. Application of Multispectral Imaging for Identification of Systemically Diseased Chicken. In Proceedings of the 2004 ASAE Annual Meeting, Ottawa, Canada, 1–4 August 2004; p. 1.
  69. Park, B.; Kise, M.; Lawrence, K.C.; Windham, W.R.; Smith, D.P.; Thai, C.N. Real-time multispectral imaging system for online poultry fecal inspection using unified modeling language. Sens. Instrum. Food Qual. Saf. 2007, 1, 45–54.
  70. Chao, K.; Chen, Y.R.; Hruschka, W.R.; Park, B. Chicken Heart Disease Characterization by Multi-spectral Imaging. Appl. Eng. Agric. 2001, 17, 99–106.
  71. Seo, Y.; Lee, H.; Mo, C.; Kim, M.S.; Baek, I.; Lee, J.; Cho, B.-K. Multispectral Fluorescence Imaging Technique for On-Line Inspection of Fecal Residues on Poultry Carcasses. Sensors 2019, 19, 3483.
  72. Gatellier, P.; Gomez, S.; Gigaud, V.; Berri, C.; Le Bihan-Duval, E.; Santé-Lhoutellier, V. Use of a fluorescence front face technique for measurement of lipid oxidation during refrigerated storage of chicken meat. Meat Sci. 2007, 76, 543–547.
  73. Abdel-Salam, Z.; Abdel-Salam, S.A.M.; Harith, M.A. Application of Laser Spectrochemical Analytical Techniques to Follow Up Spoilage of White Meat in Chicken. Food Anal. Methods 2017, 10, 2365–2372.
  74. Yu, F.; Xue, L.; Liu, M.-h.; Li, J. Preliminary study of laser-induced fluorescence spectroscopy detect chicken meat tenderness. In Proceedings of the 2nd International Conference on Information Science and Engineering, Hangzhou, China, 4–6 December 2010; pp. 6771–6774.
  75. Cho, B.-K.; Kim, M.S.; Chao, K.; Lefcourt, A.M.; Lawrence, K.; Park, B. Detection of Fecal Residue on Poultry Carcasses by Laser Induced Fluorescence Imaging. J. Food Sci. 2009, 74, E154–E159.
  76. Wold, J.P.; Kvaal, K. Mapping Lipid Oxidation in Chicken Meat by Multispectral Imaging of Autofluorescence. Appl. Spectrosc. 2000, 54, 900–909.
  77. Cuan, K.X.; Zhang, T.M.; Huang, J.D.; Fang, C.; Guan, Y. Detection of avian influenza-infected chickens based on a chicken sound convolutional neural network. Comput. Electron. Agric. 2020, 178, 105688.
  78. Yumono, F.; Subroto, I.M.I.; Prasetyowati, S.A.D. Artificial Neural Network for Healthy Chicken Meat Identification. IAES Int. J. Artif. Intell. (IJ-AI) 2018, 7, 63–70.
  79. Taheri-Garavand, A.; Fatahi, S.; Shahbazi, F.; De La Guardia, M. A nondestructive intelligent approach to real-time evaluation of chicken meat freshness based on computer vision technique. J. Food Process. Eng. 2019, 42, e13039.
  80. Wang, X.; Xu, J.; Liu, M.H.; Zhao, J.H.; Hong, Q. Determination of Gentamicin Residual in Duck Meat Using Fluorescence Analysis Method. Adv. Mater. Res. 2014, 1033–1034, 638–642.
  81. Wang, P.; Hong, Q.; Liu, M.; Yuan, H.; Peng, Y.; Zhao, J.; Pengwei, W.; Qian, H.; Muhua, L.; Haichao, Y.; et al. Rapid detection of doxycycline content in duck meat by using silver nanoparticles and alkylphenols polyoxyethylene enhanced fluorescence of europium complex. Spectrosc. Lett. 2016, 49, 563–567.
  82. Zhao, J.-H.; Yuan, H.-C.; Liu, M.-H.; Xiao, H.-B.; Hong, Q.; Xu, J. Rapid determination of tetracycline content in duck meat using particle swarm optimization algorithm and synchronous fluorescence spectrum. Spectrosc. Spect. Anal. 2013, 33, 3050–3054.
  83. Zhao, J.H.; Bin Xiao, H.; Yuan, H.C.; Hong, Q.; Liu, M.H. Application of Three-Dimensional Fluorescence Spectroscopy Coupled with ATLD in Rapid Determination of Triazophos Content in Duck Meat. Appl. Mech. Mater. 2014, 651–653, 362–366.
  84. Jiang, X.; Muhua, L.; Haichao, Y. A study on determination of neomycin residue in duck by fluorescence method. Acta Agric. Univ. Jiangxiensis 2013, 35, 635–640.
  85. Xiao, H.-B.; Zhao, J.-H.; Yuan, H.-C.; Xu, J.; Li, Q.; Liu, M.-H. Prediction of Carbofuran Residue in Duck Meat by Synchronous Fluorescence Spectroscopy Based on Support Vector Regression (SVR). J. Instrum. Anal. 2013, 3, 357–361.
More
Video Production Service