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drivers of soil respiration of root and microbial ... - Unitus DSpace

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(C0k) was negatively affected by the treatment indicating a different quality or different sources <strong>of</strong><br />

decomposing substrates with respect to UM <strong>soil</strong>s (Riffaldi et al., 1996).<br />

All these evidences support the hypothesis that microorganisms decreased their<br />

mineralization activity in MG <strong>soil</strong>s as other easily available energy sources were present.<br />

It is widely documented that the <strong>soil</strong> metabolic quotient (qCO2) is elevated when the <strong>soil</strong><br />

<strong>microbial</strong> biomass is operating inefficiently <strong>and</strong> is diverting a high proportion <strong>of</strong> C to maintenance<br />

requirements than biosynthesis (Anderson <strong>and</strong> Domsch, 1985).<br />

In our results qCO2 <strong>and</strong> <strong>soil</strong> enzymatic activity were significantly lower in MG plots <strong>and</strong><br />

suggested that the increase <strong>of</strong> easily available C in the rhizosphere <strong>of</strong> defoliated plants, resulting<br />

from a short-term flux <strong>of</strong> photoassimilate C below-ground, decreased the maintenance energy<br />

requirements <strong>and</strong> shifted the energy from maintenance to biosynthesis processes as the increase <strong>of</strong><br />

qmic also demonstrated (Bardgett et al., 1998; Holl<strong>and</strong> et al., 1996; Dilly, 2005). According to<br />

Schjonning et al. (2002) the decrease in qCO2 <strong>and</strong> specific enzyme activity indicates: a) a more<br />

efficient <strong>microbial</strong> community <strong>and</strong> b) a better use <strong>of</strong> the available organic substrates. Higher C use<br />

efficiency under defoliation was also reported by Guitian <strong>and</strong> Bardgett (2000) <strong>and</strong> Uhlirova et al.<br />

(2005).<br />

In our study almost all enzymes, involved in the cycling <strong>of</strong> S, P <strong>and</strong> C have demonstrated to<br />

be valid indicators <strong>of</strong> changes under management practices <strong>and</strong> have diminished its activity in<br />

managed <strong>soil</strong>. Only ß-cellobiohydrolase <strong>and</strong> arylsulphatase didn’ t show a significant decrease in<br />

MG plots, even so the negative trend for these enzymes was also observed. More likely that<br />

enhanced <strong>root</strong> exudation, leading to a larger supply <strong>of</strong> easily available C <strong>and</strong> energy sources to<br />

<strong>microbial</strong> communities resulted in general suppression <strong>of</strong> decomposition activities just after the<br />

mowing procedure. A significant relationship between SEI <strong>and</strong> qCO2 (Fig.14b) could be used as an<br />

extra prove <strong>of</strong> the bacterial community “ relax” in terms <strong>of</strong> C gaining in that period. N-acetyl-ß-<br />

glucosaminidase <strong>and</strong> arylsulphatase are also considered as indirect indicators <strong>of</strong> the presence <strong>of</strong> the<br />

fungal biomass because sulphate esters (substrates <strong>of</strong> arylsulphatase) <strong>and</strong> chitin are major<br />

components in fungal cells (B<strong>and</strong>ick <strong>and</strong> Dick, 1999). These could suggest a presence <strong>of</strong> a more<br />

efficient <strong>microbial</strong> community in the managed plots.<br />

The enhanced N mineralization activity just after the mowing <strong>and</strong> increase in the activity <strong>of</strong><br />

leucine amino-peptidase (involved in the N cycling) suggest that in grassl<strong>and</strong> community the<br />

defoliation practise stimulated the flow <strong>of</strong> C to <strong>root</strong>s <strong>and</strong> into the <strong>soil</strong>, increased the size <strong>of</strong><br />

<strong>microbial</strong> community, which in turn stimulated potential net N mineralization rates. Herbivores for<br />

example <strong>of</strong>ten enhance <strong>soil</strong> N cycling (McNaughton et al., 1997) which can result in the improved<br />

N availability to plants. In particular key <strong>microbial</strong>ly mediated processes involved in <strong>soil</strong> N cycling<br />

(nitrification, denitrification <strong>and</strong> N2-fixation) that largely control the balance the forms <strong>of</strong> <strong>soil</strong><br />

113

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