For sufficiently strong scattering by randomly-distributed imperfections th
e integrated intensity of a wave initiated at some starting point becomes l
ocalized within some finite distance. We discuss how this Anderson localiza
tion can be self-induced. with possible enhancement by magnetic ordering, i
n light actinide systems. This mechanism provides an nb initio based predic
tion, in close agreement with experiment, of the variation of the magnetic
ordering temperatures and low-temperature ordered moments in a number of ur
anium compounds which are driven by alloying through a phase transition fro
m non-magnetic behaviour to strong magnetic ordering. This mechanism also e
xplains the phase transition to the delta face-centred-cubic (fcc) structur
e at 592 K in elemental plutonium, which has a low-temperature alpha monocl
inic structure, and the substantial depression of melting temperature of pl
utonium and neptunium with respect to neighbouring elements. Both the stron
gly magnetically-ordered uranium systems and elemental plutonium in the fee
delta phase are described by the if electronic behaviour of a random-local
ized-fluctuating-site (RLFS) solid-solution-like phase. The physical pictur
e developed here shows that hybridization treated via the Coqblin-Schrieffe
r resonant-scattering point of view (pertinent in the weak hybridization re
gime) provides the physical connection (under certain conditions described
herein, an actual phase transition) between localized (i.e. coupled magneti
c ions) magnetism and strongly-correlated extremely-narrow band behaviour c
haracterized as heavy fermion behaviour in solids. Furthermore, the overall
physical picture thus provided for the intermediate delocalized regime of
transition-shell electron behaviour (comprising the two subregimes of RLFS
random solid-solution-like behaviour and extreme-narrow-band heavy fermion
behaviour, respectively) provides the physical connection between localized
(e.g. heavy rare earth) and itinerant (e.g. nickel) magnetism.