“…Therefore, it was not possible to count the number of interference fringes along an edge of the crystal, even using an immersion oil, in order to deduce an approximate value of the optical retardation Conoscopy, on the (llO)cub plate (t= llj.l.m), with crossed polars, using immersion oil (ne= 1.518), high numerical aperture (NA = 1.40 oil) front lens on the condenser and high numerical aperture objective (100 x/1.30 oil) was an invaluable help to deduce the interference order at room temperature, even though the melatope, the trace of the optical axis, was outside the field of view. By observing the motion of the isogyre when rotating the microscope stage, thus rotating the crystal, it was deduced that the first to the fifth isochromes for green light (551 nm) and the first to the fourth isochromes for red light (643 nm) were inside the conoscopy field of view ( (2) where B=_aA35.3° is the angle between the optical axis (OA// Ps) and the normal (N) to the (llO)cub platelet. Thus:…”