A very different behaviour pattern has been reported for glaciers in certain, but not all, areas.
The crazy-paving pattern was initially described as a pathognomonic sign of alveolar proteinosis; however, nowadays, this pattern has been reported in a variety of acute and chronic diseases as summarised in Table 1 [2, 5, 6, 7, 8].
Netting on melon surface, a wound-healing network pattern, has been reported results from a series of histological and biochemical processes (Keren-Keiserman et al. 2004; Puthmee et al. 2013).
A similar XRD pattern has been reported for crab, shrimp, krill and insects in earlier studies (Yen et al. 2009; Sajomsang and Gonil 2010; Wang et al. 2013; Liu et al. 2010; Liu et al. 2012).
A highly variable damage pattern has been reported in a particular basin due to the physical phenomenon like double-resonance [1, 2], basin generated surface waves [3, 4, 5, 6, 7, 8, 9], basement focusing effects [10, 11, 12] and basin-transduced surface waves [13, 14, 15, 16].
A similar pattern has been reported for yeast LAG1[43] and for C. elegans SKN-1.
Transgene in different tissues of transgenic animals generated by pronuclear microinjection observed a mosaic pattern has been reported [50], [51].
This size pattern has been reported previously for several solubilized olfactory receptors expressed in Sf9 and mammalian cells [26] [28].
This type of mixed pattern has been reported previously in islet electrical activity [30], [31], intracellular calcium [8], [20], [32], and in oxygen tension [33].
In comparison, A. thaliana maintains highly induced levels of JA for at least 4 h after wounding [28], although a biphasic accumulation pattern has been reported with induced levels increasing even days after a single wounding [29].
This type of localization pattern has been reported for other worm mitochondrial membrane proteins including another member of the TOMM complex [17], [20] and it was consistent with the expected role of TOMM-40.
