“…For biological samples, two‐photon fluorescence microscopy has become a well‐established technique that allows for large penetration depths (∼mm) and a minimum of light‐induced damage as the interaction is essentially confined by the focal volume. Likewise, second‐harmonic (SH) generation microscopy has shown great potential in the imaging of photonic materials down to a nanoscale (Vohnsen & Bozhevolnyi, 2001; Vohnsen et al ., 2001; Labarthet & Shen, 2003; Zayats & Smolyaninov, 2004), to reveal local symmetries in biological samples (Moreaux et al , 2000), visualization of muscle tissues (Freund & Deutsch, 1986; Chu et al ., 2003) and the fibril organization in collagen‐rich tissues such as skin (Palero et al ., 2006), the cornea and the sclera of the eye (Hochheimer, 1982; Yeh et al ., 2002; Han et al ., 2004; Han et al ., 2005; Tan et al ., 2005; Teng et al ., 2006; Morishige et al ., 2007; Svoboda et al ., 2007; Vohnsen & Artal, 2007). Likewise, SH imaging has been successfully used to image the ex vivo optic nerve head (Brown et al ., 2007) with important implications for glaucoma analysis.…”