The interplay of irreversible reactions and deformation during regional metamorphism was analyzed in the reaction zones between rodingite and serpentinite. Rodingites are leucocratic rocks found commonly in serpentinites and are considered metasomatic products of Ca-rich fluid. Rodingites occur ubiquitously in serpentinite from the Nomo metamorphic rocks, western Kyushu, a Cretaceous accretionary complex of greenschist to epidote-amphibolite facies condition. We used the singular value decomposition (SVD) method to analyze rodingitization reactions based on mineral compositions of a rodingite sample and a possible protolith (clinopyroxene gabbro). The resultant reaction implied that the rodingite was formed due to the addition of considerable amounts of CaO and H 2 O to the protolith, whereas other components such as SiO 2 , AF (Al 2 O 3 + Fe 2 O 3 ), and FM (FeO + MgO) were conserved. The Nomo rodingites are associated with reaction zones between serpentinite. A careful study on the compositional variations of diopside and chlorite in the rodingite, serpentinite, and the reaction zones between them showed a disequilibrium crystallization of diopside in the reaction zone. Diopside shows a serrated variation in composition across the reaction zone together with disequilibrium signature within grains (composite grain consisting of Fe-rich and Fe-poor parts). These features clearly indicate that diopside crystallized in a relatively short period compared to the metamorphism by irreversible reactions. Another conspicuous feature is that perovskite occurs in some reaction zones, whereas titanite is common in rodingites; this indicates that the reaction zone is poorer in SiO 2 . The tremolite veins are typically derived from the reaction zone into serpentinite; showing this is a good example of hydrofracturing associated with the formation of the reaction zone. All the reactions obtained by the SVD method that contribute to the formation of the reaction zones consumed CaO and evolved H 2 O, strongly suggesting that the hydrofracturing is caused by a rapid increment of fluid pressure during the progression of the reactions. The reactions consumed considerable amounts of SiO 2 in the reaction zone, which is consistent with the occurrence of perovskite, and the conservation of AF and FM components.