Raman scattering spectroscopy and elastic light scattering intensity (ESLI) were used to simultaneously measure levels of Ca-dipicolinic acid (CaDPA) and changes in spore morphology and refractive index during germination of individual B. subtilis spores with and without the two redundant enzymes (CLEs), CwlJ and SleB, that degrade spores' peptidoglycan cortex. Conclusions from these measurements include: 1) CaDPA release from individual wild-type germinating spores was biphasic; in a first heterogeneous slow phase, T lag , CaDPA levels decreased ∼15% and in the second phase ending at T release , remaining CaDPA was released rapidly; 2) in L-alanine germination of wild-type spores and spores lacking SleB: a) the ESLI rose ∼2-fold shortly before T lag at T 1 ; b) following T lag , the ESLI again rose ∼2-fold at T 2 when CaDPA levels had decreased ∼50%; and c) the ESLI reached its maximum value at ∼T release and then decreased; 3) in CaDPA germination of wild-type spores: a) T lag increased and the first increase in ESLI occurred well before T lag , consistent with different pathways for CaDPA and L-alanine germination; b) at T release the ESLI again reached its maximum value; 4) in L-alanine germination of spores lacking both CLEs and unable to degrade their cortex, the time ΔT release (T release -T lag ) for excretion of ≥75% of CaDPA was ∼15-fold higher than that for wild-type or sleB spores; and 5) spores lacking only CwlJ exhibited a similar, but not identical ESLI pattern during L-alanine germination to that seen with cwlJ sleB spores, and the high value for ΔT release .