Amphiboles are hydrous minerals present in the altered oceanic crust and play a vital role in transporting hydrophile elements including halogen into the deep mantle via subduction of oceanic plates (Debret et al., 2016; Ito et al., 1983). The crystal structure of amphibole consists of corner-sharing tetrahedral units linked to form double chains and edge-sharing octahedral units. The octahedral strip is sandwiched between two tetrahedral double chains with their apices pointing toward each other forming an I-beam. These minerals also contain ∼2 wt% water crystallographically bound as hydroxyl (OH −) units. The interaction of saline seawater with oceanic crust often helps to incorporate Cl and F into the amphibole crystal structure. These halogen ions, Cl − and F − readily substitute for the hydroxyl (OH −) units (Kendrick et al., 2011). As the subducting slabs experience higher temperatures at depths, hydrous minerals including amphibole dehydrate. And upon dehydration, Cl and F in the amphibole crystal structure are likely to partition into the released aqueous fluid. However, based on experimental results it seems that Cl is likely to partition into aqueous fluid far more easily than F (Bernini et al., 2013; Fabbrizio et al., 2013a, 2013b). When amphibole or apatite is present with an aqueous fluid, F partitions into these minerals instead of the fluid phase