The faces of selected blocks were scanned using an Epson V600 flatbed scanner at high resolution (1,200 dots per inch [DPI]). These scans were used to visually identify areas and points of interest for subsequent microdrilling and aDNA analysis. Between 28 and 31 points were chosen from each face with a focus of targeting 1) bone, 2) coprolite or organic phosphate, and 3) rock fragment. In addition, sediment matrix was sampled in areas where no microfeatures were visible.
V600 flatbed scanner
Manufactured by Epson
The Epson V600 is a flatbed scanner that can digitize photographs, documents, and other physical media. It features a maximum optical resolution of 6400 dpi and supports a variety of media types including reflective and transparent originals.
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Lab products found in correlation
2 protocols using v600 flatbed scanner
1
Microstructural Analysis of Archaeological Samples
2
Arabidopsis Growth and Root Analysis
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A. thaliana ecotype Columbia‐0 was used as the wild type in all described studies. Plants were grown in a controlled environment growth chamber with a 16 hr light period at 22°C and ~100 µmol/m2 s‐1 illumination and an 8 hr dark period at 18°C. Seed stratification was performed for 2–3 days at 4°C. For plant growth on soil, Sungro Sunshine Mix #1 was used. For root growth assays, seeds were initially germinated on plates containing half‐strength Murashige and Skoog medium, 1% sucrose, pH 6.0. After 5 days, seedlings were transferred to vertically oriented plates containing Somerville and Ogren medium (5 mM KNO3, 2.5 mM KH2PO4 [pH5.6], 2 mM MgSO4, 2 mM Ca[NO3]2, 50 μM Fe‐EDTA, and the reported micronutrient mix) (Somerville & Ogren,1982 ) with no exogenous carbon source. To analyze root system architecture, plates were scanned using an Epson V600 flatbed scanner after 6–7 days of vertical growth (11‐ to 12‐day‐old plants), and images were analyzed using the EZ‐Root‐VIS software pipeline (Shahzad et al., 2018 ).
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A. thaliana ecotype Columbia‐0 was used as the wild type in all described studies. Plants were grown in a controlled environment growth chamber with a 16 hr light period at 22°C and ~100 µmol/m2 s‐1 illumination and an 8 hr dark period at 18°C. Seed stratification was performed for 2–3 days at 4°C. For plant growth on soil, Sungro Sunshine Mix #1 was used. For root growth assays, seeds were initially germinated on plates containing half‐strength Murashige and Skoog medium, 1% sucrose, pH 6.0. After 5 days, seedlings were transferred to vertically oriented plates containing Somerville and Ogren medium (5 mM KNO3, 2.5 mM KH2PO4 [pH5.6], 2 mM MgSO4, 2 mM Ca[NO3]2, 50 μM Fe‐EDTA, and the reported micronutrient mix) (Somerville & Ogren,
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