Eos 5d digital camera

Compressive test specimens were fabricated into cylinders (30 mm long, 19.85 mm diameter) by casting in an aluminum mold. Testing was performed using an AGS-X at a rate of 10 mm per min. Specimens were stored at 37 °C. DSC curves were prepared using a TA DSC Q2000 at a rate of 3 °C per min. Viscosity was measured using an NDJ-9S rotational viscometer in 10 mL glass sample bottles at a speed of 30 r·min⁻¹. Thermal images were recorded using a FLIR A6703sc 470. Macroscopic images of the polymers were recorded using a Canon EOS 5D digital camera. ¹H-NMR spectra were obtained using an Avance III HD 600 MHz.

An analysis of 578 cases (medical and outpatient records and reports of pathoanatomical and forensic autopsies) recorded in healthcare facilities treating opisthorchiasis patients with a hyperendemic focus was carried out. The average age of patients was 49.7 ± 3.4 years, and the average age of those who died was 52.3 ± 2.9 years. Males (n=217) and females (n=361) were included, with a female to male ratio of 1.6 : 1. A total of 110 hearts as well as livers (Figures 1 and 2) from deceased patients were subjected to morphological study, including hearts from those with sudden cardiac death (n=16). The preparations were stained with haematoxylin and eosin and van Gieson's stain using the Selye and Slinchenko methods. The degree of cellular infiltration and sclerotic processes was recorded by determining the index of the area occupied by cellular elements and fibrous structures (%), as well as their proportion in the composition of infiltrates. The stained preparations were subjected to light-optical analysis, and the images of histological preparations, taken with a microscope and Canon EOS 5D digital camera, were saved on a computer. Using the UTHSCSA Image Tool for Windows 3.0 program, the area of metabolic myocardial necrosis was determined. Mathematical and statistical processing of the data was performed on a personal computer using Statistica 6.1 software (Statsoft®).

A geometric morphometric analysis was conducted on a subset of Parvancorina specimens (N = 57) from Parv Bed in order to assess morphological variation; the remainder of the specimens from Parv Bed (N = 36) are not preserved well enough for the purposes of accurate landmarking and semi-landmarking. To conduct the semi-landmark analysis, the following steps were taken: Specimen latexes were coated with ammonium chloride, then photographed using a Canon EOS 5D digital camera with a Canon MP-E 65 mm 1–5x macro lens. Landmarking and semi-landmarking (see Supplementary Fig. S4) was conducted using the Thin-Plate Spline (tps) suite (http://life.bio.sunysb.edu/morph/index.html). A tps file was constructed using tpsUtil64 (v.1.7)62 . The tps file was imported into tspDig2 (v.2.26)63 , which was used to place the five landmarks and 80 semi-landmarks around the Parvancorina anchor structure and populate the tps file with the semi-landmark and landmark data. The tps file was imported into an R environment58 . The ‘geomorph’ package64 was used to conduct the Procrustes Superposition and Principal Components Analysis (PCA) of the superimposed data, producing Fig. 2B.