In order to quantify changes in these parameters between the initial basal (dark), stimulated (light), and recovery (dark) imaging intervals, the distributions were normalized by the median value of the basal interval.
These clasts were scoured and peeled away from the basal dark mud/silt level upper surface of the dark silt and stretched toward the SE, so that at their extremity, numerous micro-clasts are liberated.
The nuclei in the superficial cell layer were clearly visible as THG-bright structures [ Fig. 2(a), 2(b) (arrowheads)], but on the contrary the nuclei were THG-dark structures within basal cells [ Fig. 2(d) (arrowheads)].
The histological and simulation results support our finding that the nucleus THG contrast was strongly influenced by the nucleus thickness and explain our observation that cell nuclei appeared THG bright in the superficial and intermediate layer, but THG-dark in the basal layer.
The bill of the curve-billed is all black, while that of Bendire's is paler down to the lower mandible, showing a dark grey with a basal area that does not feature a stark contrast.
The sub-basal membrane area appeared as a dark zone in between the basal cell layer and the higher reflective papillary dermis.
Signals were scored in 100 epithelial nuclei per specimen, in at least four distinct areas: 50 nuclei in the superficial layer (larger cells, closer to the lumen) and 50 nuclei in the basal layer (darker HE-stained nuclei, smaller cells, closer to the muscular layer).
Bar graph plots show the distribution of the six TNBCtype subtypes: basal-like 1 (red), basal-like 2 (dark red), immunomodulatory (dark green), mesenchymal-like (pink), mesenchymal stem-like (magenta), luminal androgen receptor (blue) and unclassified tumours (yellow), within each cluster.
The total current is attributed to three components: the basal thermal or dark current (γIm), an increase in thermal current with increasing irradiance (βImH), and the photocurrent (Im tanh (αH/Im)).
The ovaries were cut crosswise into 3 4 mm discs and cultured in the dark at 25 °C on BM basal medium supplemented with 9% sucrose and 1.0 mg/L NAA, with pH adjusted to 5.8.
