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Applied and Environmental Microbiology, June 2001, p. 2603-2609, Vol. 67, No. 6
Swiss Federal Institute of Technology (ETH
Zürich), Institute of Terrestrial Ecology, Soil Biology,
Schlieren,1 and Paul Scherrer
Institute, Laboratory of Atmospheric Chemistry,
Villingen-PSI,3 Switzerland; and New
Jersey Institute of Technology, Department of Chemical Engineering,
Chemistry and Environmental Sciences, and Rutgers University,
Department of Biological Sciences, Newark, New
Jersey2
Received 17 November 2000/Accepted 9 March 2001
High-N2-fixing activities of Frankia
populations in root nodules on Alnus glutinosa improve
growth performance of the host plant. Therefore, the establishment of
active, nodule-forming populations of Frankia in soil is
desirable. In this study, we inoculated Frankia strains
of Alnus host infection groups I, IIIa, and IV into soil
already harboring indigenous populations of infection groups (IIIa,
IIIb, and IV). Then we amended parts of the inoculated soil with leaf
litter of A. glutinosa and kept these parts of soil
without host plants for several weeks until they were spiked with [15N]NO3 and planted with seedlings of
A. glutinosa. After 4 months of growth, we analyzed
plants for growth performance, nodule formation, specific
Frankia populations in root nodules, and N2
fixation rates. The results revealed that introduced
Frankia strains incubated in soil for several weeks in
the absence of plants remained infective and competitive for nodulation
with the indigenous Frankia populations of the soil.
Inoculation into and incubation in soil without host plants generally
supported subsequent plant growth performance and increased the
percentage of nitrogen acquired by the host plants through
N2 fixation from 33% on noninoculated, nonamended soils to
78% on inoculated, amended soils. Introduced Frankia strains representing Alnus host infection groups IIIa
and IV competed with indigenous Frankia populations,
whereas frankiae of group I were not found in any nodules. When grown
in noninoculated, nonamended soil, A. glutinosa plants
harbored Frankia populations of only group IIIa in root
nodules. This group was reduced to 32% ± 23% (standard deviation) of
the Frankia nodule populations when plants were grown in
inoculated, nonamended soil. Under these conditions, the introduced
Frankia strain of group IV was established in 51% ± 20% of the nodules. Leaf litter amendment during the initial
incubation in soil without plants promoted nodulation by frankiae of
group IV in both inoculated and noninoculated treatments. Grown in
inoculated, amended soils, plants had significantly lower numbers of
nodules infected by group IIIa (8% ± 6%) than by group IV (81% ± 11%). On plants grown in noninoculated, amended soil, the original
Frankia root nodule population represented by group IIIa
of the noninoculated, nonamended soil was entirely exchanged by a
Frankia population belonging to group IV. The
quantification of N2 fixation rates by 15N
dilution revealed that both the indigenous and the inoculated Frankia populations of group IV had a higher specific
N2-fixing capacity than populations belonging to group IIIa
under the conditions applied. These results show that through
inoculation or leaf litter amendment, Frankia
populations with high specific N2-fixing capacities can be
established in soils. These populations remain infective on their host
plants, successfully compete for nodule formation with other indigenous
or inoculated Frankia populations, and thereby increase
plant growth performance.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.6.2603-2609.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Effect of Inoculation and Leaf Litter Amendment on
Establishment of Nodule-Forming Frankia Populations
in Soil

*
Corresponding author. Mailing address: ETH
Zürich, Institute of Terrestrial Ecology, Soil Biology,
Grabenstrasse 3, CH-8952 Schlieren, Switzerland. Phone: 41 1 633 6042. Fax: 41 1 633 1122. E-mail: pelz{at}ito.umnw.ethz.ch.
Present address: Department of Chemical Engineering, Chemistry and
Environmental Sciences, New Jersey Institute of Technology, and
Department of Biological Sciences, Rutgers University, 101 Warren
Street, Smith Hall 135, Newark, NJ 07102-1811.
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