Aluminosilicate garnet is an excellent phase to research solid-solution behavior in silicates.Natural almandine-pyrope, {Fe 2+ 3x ,Mg 3-3x }[Al 2 ](Si 3 )O 12 , and almandine-spessartine, {Fe 2+ 3x ,Mn 2+ 3-3x }[Al 2 ](Si 3 )O 12 , crystals were measured by UV/Vis/NIR (~29000 to 10000 cm -1 ) optical absorption spectroscopy using a microscope. The spectra and changes in energy of a number of Fe 2+ and Mn 2+ spin-forbidden electronic transitions of different wavenumber were analyzed as a function of garnet composition across both binaries. The spectra of Alm-Pyp garnets are complex and show a number of Fe 2+ and Fe 3+ transitions manifested as overlapping absorption bands whose intensities depend on composition. There are differences in energy behavior for the various electronic transitions, whereby lower wavenumber Fe 2+ transitions decrease slightly in energy with increasing pyrope component and those of higher wavenumber increase. The spectra of Alm-Sps solid solutions show both Fe 2+ and Mn 2+ spin-forbidden bands depending upon the garnet composition. The variations in energy of the different wavenumber Fe 2+ transitions are unlike those observed in Alm-Pyp garnets. The three lowest wavenumber electronic transitions appear to vary the most in energy across the Alm-Sps join compared to those at higher wavenumber. Four narrow and relatively intense Mn 2+ spin-forbidden bands between 23000 and 25000 cm -1 can be observed in many Sps-Alm garnets. Their transition energies may increase or decrease across the join, but scatter in the data prohibits an unequivocal determination. A consistent crystal-chemical model and Fe 2+ -O bond behavior, based on published diffraction and spectroscopic results, can be constructed for the Alm-Pyp binary but not for the Alm-Sps system. The spectra of the former garnets often show the presence of high wavenumber spin-forbidden bands that can be assigned to electronic transitions of Fe 3+ occurring at the octahedral site. The most prominent band lies between 27100 and 27500 cm -1 depending on the garnet composition. Fe 3+ -O 2bonding is analyzed using Racah parameters. State-of-the-art electronic structure calculations are needed to understand the precise physical nature of the electronic transitions in garnet and to interpret better UV/Vis/NIR spectra.