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Chroma meter

Manufactured by Konica Minolta
Sourced in Japan

The Chroma Meter is a compact, portable device designed for measuring and analyzing color parameters. It accurately captures color data, providing precise measurements of various color attributes such as chromaticity, luminance, and color temperature. The Chroma Meter is a versatile tool for applications that require accurate color evaluation and analysis.

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39 protocols using chroma meter

1

Suhuai Pig Meat Color Analysis

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All animal procedures were performed in accordance with the Guidelines for Care and Use of Laboratory Animals of Nanjing Agriculture University and approved by the Animal Ethics Committee of Nanjing Agriculture University. A total of 300 healthy Suhuai pigs (i.e., 194 castrated barrows and 106 sows) with the same market weight (80–90 kg) and approximately 7–8 months old were reared at the Huaiyin Breeding Farm (Huaian, China) under the same feeding conditions and slaughtered at Sushi Meat Products Co., Ltd. (Huaian, China).
Ear tissues from the end of the right ear were collected and stored in 75% alcohol for DNA extraction. Samples of the LD, SOL, psoas major (PM), masseter (MA), and biceps femoris (BF) muscles were collected for RNA extraction from four randomly selected healthy Suhuai pigs with similar body weight and age. LD muscle samples from the last rib of the carcass were collected and used to determine meat color. In China, traditional hot fresh meat is usually marketed immediately after slaughter, whereas chilled fresh meat is often cooled quickly to a stable 0–4°C within 24 h postmortem and maintained at this temperature until sold to the consumer (21 (link)). Therefore, meat color (L*a*and b*) was measured on the last rib at 2 (room temperature) and 24 h (4°C) postmortem using a chromameter (Minolta Camera Co., Osaka, Japan).
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2

Pericarp Penetration Testing of Tomato Fruit

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Example 6

Pericarp Penetration Test (PPT)

Phenotypic analysis was carried out on the S.pennellii ILs grown under glasshouse conditions in the UK. A 6 mm transverse section was cut from each fruit and the maximum load (force required to penetrate the pericarp tissue at 10 mm/minute) was measured using a Lloyd Instrument LRF+ machine (Lloyd, UK) equipped with a 10 N load cell and 1.6 mm probe. Measurements were taken separately from the outer and inner pericarp in duplicate. Fruit weight, truss position and colour were also recorded. Colour was measured using a Chroma Meter (Minolta).

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3

Evaluating Meat Color Attributes

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The color values of CIELAB Color System (1976), L* (lightness) a* (redness), and b* (yellowness), were determined on the breast muscles 15 min after slaughter using a Chroma meter (Konica Minolta, CR-400-Japan). As described by Valizadeh et al. (33 (link)) and Qaid et al. (34 (link)), values for L*, a*, and b* were converted to estimate the saturation index, total color change (ΔE), hue angle, browning index (BI), and whiteness index (WI). These parameters could provide more accurate assessment of how consumers perceive meat color.
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4

Ham Surface Color Measurement

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The ham color was assessed by taking at least 5 random measurements from the surface of the different ham samples using a Minolta Chroma Meter fitted with a CR-300 measuring head (Minolta, Osaka, Japan). The CIE (Commission Internationale de l’Eclairage) L*, a*, b*, colorimetry system was used for color determination with L* indicating lightness, a* indicating redness and b* indicating yellowness. Measurements of the instrument were standardized with respect to a white calibration plate. Color measurements avoiding the area with excess fat were taken and the values were recorded in order to determine C* (chroma).
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5

Precise Color Measurement Technique

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Initial color for all specimens was measured by CIE values, L* (lightness), a* (red-green coordinate), and b* (yellow-blue coordinate) against a white background and a black background using a Chroma Meter (CR-221; Minolta, Osaka, Japan). The device has a 3-mm diameter measuring area and uses 45-degree circumferential illumination and a 0-degree viewing angle geometry for measuring precise areas of surfaces. The color values for each background alone were as follows, based on three individual measurements: white background (L* = 93.879 ± 0.106, a* = 2.148 ± 0.044, b* = −5.757 ± 0.173) and black background (L* = 12.197 ± 0.219, a* = −0.010 ± 0.084, b* = −1.075 ± 0.077). Calibration of the chromameter was performed before each measuring session.
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6

Color Analysis of Spent Hen Meat Patties

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The color values of spent hen meat patties from each group were measured by using a Chroma Meter (Konica Minolta, CR 410; Marunouchi, Japan), with an illuminant D65, the aperture size of 11 mm, an observer of 10°, and calibrated against a white calibration plate, using the method outlined by Shin et al. [19 (link)]. From each sample, three readings were quantified and the mean values were expressed as lightness (L*), redness (a*), and yellowness (b*).
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7

Comprehensive Analysis of Fruit Physico-Chemical Properties

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Fruit hardness was measured by a TMS-Pilot Precision texture analyzer (Food Technology Corporation, Virginia, USA), and the fruit color difference was measured by a color difference meter from CHROMA METER (KONICA MINOLTA SENSING INC. Japan).
Lycopene was extracted with reference to Salvia-Trujillo and McClements (Salvia-Trujillo and McClements, 2016 (link)), total phenolic compounds were extracted with reference to Toor and Savage (Toor and Savage, 2005 (link)), and total flavonoids according to Jia et al. (Jia et al., 1999 (link)), while carotenoids were extracted by the acetone method and then all were determined spectrophotometrically. The contents of pectin, vitamin C, soluble protein, soluble sugar and acidity were also determined by spectrophotometrically.
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8

Evaluating Chicken Breast Meat Quality

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Briefly, the L* values of each chicken breast meat were determined in triplicate using a chromameter (Minolta Camera Co., Osaka, Japan) as described by Li et al [5 ]. The pH values were measured by inserting an electrode of a portable pH meter (Orion 3-star, Dallas, TX, USA) at three different locations of each breast meat [12 (link)]. Drip loss of meat was evaluated at 24 h postmortem. Each breast meat (about 20 g) was placed in a sealed polyethylene package and kept at 4°C for 24 h. Drip loss was expressed as a percentage of the weight loss over initial meat sample weight.
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9

Evaluating Tea Color Characteristics

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The tea samples’ color characteristics were evaluated using the Hunter L* (whiteness/darkness), a* (redness/greenness), and b* (yellowness/blueness) parameters, which were adjusted to a standard observer angle of 10° and D‐65 illumination type. The Chroma Meter (model CR‐5, Konica Minolta, Osaka, Japan) was used to measure the color. To perform the measurements, 5 mL of tea sample was placed in a rectangular glass cell (50 × 38) while maintaining its temperature. Prior to analysis, the instrument's standardization was conducted using a black plate (Mao et al., 2021 (link)).
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10

Evaluating pH and Color of Ham with Essential Oils

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The pH value of the samples was recorded with a digital pH meter (HI 2211 pH-ORP Meter, HANNA Instruments, Woonsocket, RI, USA), during storage at different temperatures at different time intervals. After finishing the microbiological analysis, the ham homogenate (stomacher homogenate) was used to measure the pH of the samples.
The color of the ham samples was evaluated by taking at least five random readings from the surface of the different samples using a Minolta Chroma Meter fitted with CR-300 measuring head (Minolta, Osaka, Japan). Measurements of the instrument were standardized with respect to a white calibration plate, every time before use. The CIE (Commission Internationale de l’Eclairage), L*, a*, b*, colorimetry system was used for color determination with L* representing lightness, a* representing redness and b* representing yellowness. All of the measurements were collected from areas on the ham surface without visual excess fat, and the values were recorded for C* (chroma) calculation using the following equation: C* = (a*2 + b*2)1/2. Values regarding control and OEOF samples (without essential oil), were common with those reported in our previous paper [52 (link)], while the results relevant to the essential oil supplemented films—OEOS (which is the purpose of this paper) are reported for first time in the current paper.
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