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Diversifying crop rotations with temporary grasslands - Université de ...

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• a remobilisation coefficient, α, <strong>de</strong>termining the potential rate of remobilisation per day (α<br />

varies according to weed species, the number and frequency of times the plant has<br />

previously been cut and the plant age or phenological stage, such as illustrated in Fig. 24);<br />

• the temperature interval between mean temperature at day j, Tmean j and the base<br />

temperature of plant growth specific of each species, Tb;<br />

<strong>de</strong>termining the speed of<br />

biochemical processes including remobilisation<br />

• a coefficient reducing the remobilisation rate when the actual leaf area, LAj-1,<br />

converges<br />

during regrowth to a threshold leaf area, LAth that <strong>de</strong>termines the point where plant<br />

growth and respiration may entirely be powered by photosynthesis. (As this threshold is<br />

actually not known, it may be assumed for simplicity that it is equal to the known leaf area<br />

might be lower, but the mo<strong>de</strong>l will<br />

before cutting: LAth = LAbefore ; in reality, LAth<br />

probably not be very sensitive to this parameter).<br />

• The differences between the sum of biomass remobilized from cutting until day j,<br />

∑ΔBMremob<br />

j, and the total quantity of remobilizable carbohydrates, which is <strong>de</strong>termined<br />

by the biomass before cutting, BMbefore,<br />

and β, a coefficient <strong>de</strong>termining the total part of<br />

biomass that may potentially be remobilized.<br />

Therefore, remobilisation will <strong>de</strong>cline and fa<strong>de</strong> out when the available reserves are <strong>de</strong>pleted or<br />

when enough new leaf area is established. The proposed formalism for simulating post-cutting<br />

regrowth is basically a mo<strong>de</strong>l <strong>with</strong> 2 unknown parameters, α and β (Tb is already known in<br />

the FLORSYS mo<strong>de</strong>l and LAth might be assumed to equal LAbefore).<br />

Both parameters, α and<br />

β, would vary according to weed species, the number of times and the frequency the plant has<br />

previously been cut and the plant age or phenological stage, and might be estimated from the<br />

data obtained in the greenhouse experiments (chapter C.III). After implementing the mo<strong>de</strong>l, an<br />

analysis of the mo<strong>de</strong>l sensitivity to these parameters will have to be performed. It seems likely<br />

that the mo<strong>de</strong>l will be highly sensitive to α <strong>de</strong>termining the remobilisation rate immediately<br />

after cutting.<br />

175

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