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12 protocols using microph 2001 ph meter

1

Fecal Sampling and pH Analysis

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Once a week, fecal samples were obtained, weighted, and dried in a stove at 60°C during 24 h. Then, feces were weighted again to calculate the percentage of humidity. For pH determination, cecal samples from days 21 and 42 were used. The measurement was performed with a micropH 2001 pH meter (Crison Instruments, Barcelona, Spain) using a 5,207 pH electrode for surfaces.
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2

Fecal and Stomach pH Measurement

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For pH determination, fecal samples from days 7–9 (middle of the study) and 14–16 (end of the study) were diluted in distilled water (up to 200 mg/mL) and gently agitated before the measurement. In contrast, stomach content samples from day 8 and 16 were measured directly without previous dilution. In both cases, pH was measured using a 5207 pH electrode for surfaces and a micropH 2001 pH meter (Crison Instruments, Barcelona, Spain).
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3

Measuring Rat Body Temperature and Fecal pH

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A TEMP JKT thermometer (Oakton, Vernon Hills, IL, USA) and an RET-3-ISO rectal probe for neonatal rats (Physitemp, Clifton, NJ, USA) were used to measure the rats’ body temperature, using peanut oil (Acofarma, Terrassa, Spain) for lubrication, as in previous studies [7 (link)]. The initial temperature was evaluated the day before the RV inoculation (the final temperature was determined 1 day after the RV inoculation and the results are expressed as the increase between them). Fecal specimens from rats during the studied period were diluted in distilled water (up to 200 mg/mL), agitated and then the pH was measured using a 5207 pH electrode for surfaces and a micropH 2001 pH meter (Crison Instruments, Barcelona, Spain).
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4

Colour and pH Analysis of Sauce

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Colour was measured by reflectance on sauce surface using a Chroma Meter II CR-200/08 (Minolta Ltd., Milton Keynes, UK) with a D65 illuminant, 2° observer angle and 50 mm aperture size. Results were expressed in CIE units: lightness (L*), redness (a*), yellowness (b*), and ΔE* [(L*day 0 − L*day 42)2 + (a*day 0 − a*day 42)2 + (b*day 0 − b*day 42)2]1/2. The pH was determined with a MicropH 2001 pH meter (Crison, Barcelona, Spain) using a Cat. 52-22 combined electrode (Ingold Electrodes, Wilmington, DE, USA).
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5

Fecal pH Measurement in Virus Samples

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Fecal samples from the peri-inoculation period of the virus were diluted in distilled water (up to 200 mg/mL) and gently agitated. Their pH was measured using a 5207 pH electrode for surfaces (Crison Instruments, Barcelona, Spain) and a micropH 2001 pH meter (Crison Instruments).
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6

Metabolomic Analysis of Fruit Tissue

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For metabolomic analysis, apple and pear fruits were cut into halves and the true fruit parts (core and seeds) were removed using a small spoon (Schnitzmesser-set Professional; Triangle, Solingen, Germany). From each half, we prepared four equal pieces including the exocarp (skin) and mesocarp (pulp) using a professional tool for fruit sculpture (Schnitzmesser-set Professional). Two pieces were frozen in liquid nitrogen and stored at −80 °C as technical replicates. The other two pieces were frozen in liquid nitrogen and powdered using an A11 basic analytical mill (IKA-Werke, Staufen, Germany) and stored at −80 °C. For quality analysis, the °Brix, pH and hardness were determined for 30 fruits as previously described [14 (link)]. Briefly, the hardness was measured with a PCE-PTR 200N sclerometer (PCE Instruments, Lucca, Italy) at four fruit positions, then six pools of five fruits were created and the juices were extracted with a mixer. A micropH 2001pH meter (Crison, Carpi, Italy) and a DBR 35 digital refractometer (Kingstic, Ningbo, China) were used to assess the pH and °Brix, respectively.
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7

pH and Color Measurement Protocol

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pH was determined with a MicropH 2001 pH meter (Crison, Barcelona, Spain) and a Cat. 52-22 combined electrode (Ingold Electrodes, Wilmington, DE, USA). CIELab colour was measured using a CR-200/08 Chroma Meter II (Minolta Ltd., Milton Keynes, UK) with a D65 illuminant, 2° observer angle and 50-mm aperture size. The results were expressed as CIELab values: lightness (L*), redness (a*) and yellowness (b*).
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8

Diarrhea Fecal and Stomach pH Measurement

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Fecal samples from the peak of diarrhea (days 7–9) and from the end of the study (days 14–16) were diluted in distilled water (up to 200 mg/mL) and agitated, whereas stomach content samples from day eight and sixteen were measured directly without previous dilution. The measure of pH was performed using a 5207 pH electrode for surfaces and a micropH 2001 pH meter (Crison Instruments, Barcelona, Spain).
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9

Soil Extract Physicochemical Characterization

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Water extracts from test soils were obtained according to the British Standard EN 12457-2 (2002) . Suspensions were prepared into 2-L glass vessels by mixing soils and deionized water at a ratio of 1:10 (w/v). Soil mixtures were thoroughly agitated on an orbital shaker Unimax 2010 (Heidolph, Germany) during 24 hours at a temperature of 20±2 ºC. After a settling period of 15 minutes, samples were centrifuged (2000 g, 10 minutes) and filtered through a 1 µm pore size membrane filter. Supernatants were kept refrigerated until use. Values of pH, Electrical Conductivity and Total Organic Carbon (TOC) were determined with a Microph 2001 ph-meter (Crison, Spain), a Ecoscan Con 5 conductivity meter (Eutech Instruments, UK) and a TOC-VCSH analyzer (SHIMADZU, Japan), respectively. A subsample of each water extract was sent to Analiza Calidad (Barcelona, Spain) for the quantification of metals and total hydrocarbons through AAS and Fourier Transform Infrared Spectroscopy (FTIR), respectively.
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10

Wax-Printed Paper-Based Electrochemical Devices

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A XEROX Colorqube 8570 printer was used to print the paper-based analytical devices following previously established protocols [23] (link). A RCT classic hot plate from IKA set at 105 ⁰C was used to melt the wax on the paper. Buffer solution pH was determined with a Crison micropH 2001 pH meter. Electrochemical measurements were performed employing a threeelectrode system connected to an Autolab PGSTAT12 potentiostat (Metrohm) controlled by Autolab GPES 4.9 software. Electrodes were connected to the potentiostat by using a commercial screen-printed electrode connector (DRP-DSC, DropSens) and a 3-pin male connector with the aid of an insulated alligator clip as illustrated in the Figure S1.
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