The paper summarizes results obtained during comparative studies of di
amondiferous mineralization in iron meteorites, ureilites, and chondri
tes. In all types of meteorites, diamond is restricted to the metallic
taenite-kamacite phase, in which it occurs together with moissanite (
SiC), daubreelite, troilite, and spinel. The diamond is specifically h
igh in its abundances of hydrogen, nitrogen, and noble gases, with a u
niform ''spectrum'' of species. The diamond of ureilites is magmatic;
it was the first phase to crystallize from the nickel-iron fluid-beari
ng melt, from which graphite and kamacite crystallized later. The latt
er mineral occurs as drop-shaped inclusions in graphite. The diamondif
erous melt of ureilites fills interstitions and veinlets. As a result
of the fluid effect of this melt, the olivine iron mole fraction decre
ases from 17 - 20 to 0, and native iron and enstatite form: Mg1.7Fe0.3
SiO4 + 0.3H(2) = 0.7Mg(2)SiO(4) + 0.3MgSiO(3) + 0.3Fe + 0.3H(2)O. The
high-pressure conditions of this effect are evident from the occurrenc
e of both diamondiferous mineralization and pyrope, which we first dis
covered in ureilites. The diamond of chondrites is restricted to the t
aenite-kamacite melt in the matrix, which actively affects the pyroxen
e-olivine chondrules. The paper describes the proposed two-stage genet
ic model for the evolution of parental meteoritic planets: stage I, un
der high pressure of the hydrogen envelopes and progressively more red
uced conditions, and stage II, after the migration of the gas envelope
s in a progressively more oxidized environment. The model explains the
relict nature of diamondiferous mineralization in chondrites, which o
riginated exclusively during stage I of planetary evolution. The progr
esively stronger effect of hydrogen on the molten meteoritic material
during this stage accounts for the coexistence of diamondiferous miner
alization and the isotopic anomalies of the chondrites. The metallic c
ompounds that formed during this stage show anomalously low oxidation
states (SiO, SiH2, SiCl2, etc.) due to reactions such as SiO2 + H-2 =
SiO + H2O. Such reactions result in that the silicates in assemblage w
ith diamond are anomalously enriched in isotopically light oxygen, for
example: 2MgO + 2Si0 + CH2 + CO = Mg2SiO4 + SiC + C + H2O. The chondr
itic assemblage of diamond and moissanite (SiC) and the occurrence of
native silicon provide evidence for the operation of such reactions du
ring diamond-forming processes.