The qualitative and quantitative distribution of Frankia strains infec
tive on Elaeagnus angustifolia L. from different depths in the same so
il (10-20 cm; 30-40 cm; 50-60 cm) were compared. The soil samples coll
ected from a natural stand devoid of Elaeagnaceae were planted with El
aeagnus angustifolia L. seedlings. All plants became nodulated, demons
trating that Frankia strains were present at least down to 60 cm in th
e soil. The decreased density of Frankia strains was correlated to the
decline of soil organic matter content with soil depth. DNA extracted
from nodules produced on Elaeagnus angustifolia L. seedlings were pol
ymerase chain reaction (PCR) characterized by amplifying the nifD-K in
tergenic spacer (IGS), using the polymerase chain reaction (PCR) follo
wed by restriction fragment length polymorphism (RFLP) analysis. This
showed the presence of seven nif-HaeIII profiles within this Frankia c
ommunity. Diversity of Frankia strains was maintained throughout the s
oil column, but the relative distribution of strains varied. Some nif-
HaeIII profiles were only found in the deeper soil. suggesting differe
nt selective advantages to withstand the constraints of soil depth. N-
15(2) experiments indicated that all the strains tested had N-2-fixing
activity, However. efficiency was not significantly different among n
odules of different nif-HaeIII profiles. Therefore, N-2-fixing activit
y does not seem to be the main factor responsible for the different di
stribution of Frankia strains at different soil depths.