The distribution and origin of diagenetic products of polycyclic quinone pigments in fossil crinoids was investigated using high-performance liquid chromatography-diode array detection-atmospheric pressure photoionization mass spectrometry (HPLC-DAD-APPI-MS). A number of characteristic highermolecular-weight polycyclic aromatic hydrocarbons (PAHs) were identified in toluene extracts of diverse crinoid samples, with 1,2,3,4,5,6-hexahydrophenanthro[1,10,9,8-opqra]perylene as the main compound. Moreover, phenanthro[1,10,9,8-opqra]perylene-7,14-dione (PPQ) and further derivatives were detected for the first time in the fossil record, representing intermediates between hydroxylated phenanthroperylene quinone pigments such as fringelite F and phenanthroperylene PAHs. The widespread presence of PPQ its derivatives and related PAHs in fossil crinoids which contain phenanthroperylene quinone pigments confirms the diagenetic formation of specific PAHs by reductive degradation of quinone pigments. (C) 2019 The Author. Published by Elsevier Ltd.