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Interactions Between Mycorrhizal Fungi and Bacteria 207<br />

tative area within a desertified semi-arid ecosystem in southeast Spain.<br />

The existing natural vegetation was a degraded shrubland, in which Anthyllis<br />

cytisoides, a drought-tolerant legume able to form symbioses with<br />

both rhizobial and mycorrhizal microsymbionts, was the dominant species<br />

(Requena et al. 1997). The experimental variables tested, as inoculants for<br />

Anthyllis cytisoides seedlings to be transplanted, involved three microsymbiont<br />

inoculation treatments, including: (1) an exotic mycorrhizal fungi<br />

from culture collection, (2) a mixture of five taxa of indigenous mycorrhizal<br />

fungi representing the natural abundance and diversity at the site,<br />

and (3) an indigenous rhizobial inoculum (Requena et al. 1997). A timecourse<br />

(every 6 months) sampling was established over 5 years after transplanting.<br />

A long-term improvement in the physicochemical properties in<br />

the soil around Anthyllis plants inoculated with a mycorrhizal inoculum<br />

based on indigenous taxa was observed. The benefits included an increased<br />

content of both N and organic matter, and in the number of hydro-stable<br />

macroaggregates.<br />

As described before, it can be assumed that the increase in N content<br />

in the rhizosphere of the legume can be accounted to an improvement in<br />

nodulation and N-fixation rates resulting from inoculation with mycorrhizal<br />

fungi (Barea et al. 1992), while increases in organic matter content<br />

and improvement in soil aggregation are due to the role of the mycorrhizal<br />

mycelium on soil structure stabilization (Miller and Jastrow 2000). Because<br />

rhizobial species are usually recognized for their ability to produce<br />

exo-polysaccharides (Spaink et al. 1998), it can be assumed that, given the<br />

Fig. 3. Time-course changes in soil aggregation in the rhizosphere of field-established nodulated<br />

plants of Anthyllis cytisoides growing under natural conditions, either noninoculated<br />

with AMF (white columns), or inoculated with G. intraradices (light gray columns), or with<br />

native AMF (dark gray columns). For each response variable, means (n = 5), not sharing<br />

aletterincommondiffersignificantly(p = 0. 05) from each other according to Duncan’s<br />

multirange test. Data points on the y-axis represent background values in the bare soil<br />

before transplanting. (Requena et al. 2001)

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