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

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A, the ‘green area remaining after cutting for photosynthesis’, would be <strong>de</strong>termined by the<br />

cutting height and by the weed plant height and morphology (vertical distribution of leaf area).<br />

Plant height and morphology will <strong>de</strong>pend on i) the weed species (functional group) opposing<br />

tall and upright weed species vs. small and creeping species, ii) the plant age and stage at<br />

cutting date (very young plants are too small and therefore not touched by the cutting etc.) and<br />

iii) the plant growth resources and growth conditions (optimal water and nutriment<br />

availabilities may e.g. lead to bigger and taller weed plants, but high light availabilities may<br />

lead to smaller plants compared to plants grown in shadow, see references in Article 4). The<br />

FLORSYS-mo<strong>de</strong>l already simulates the weed plant height and the vertical distribution of leaf<br />

area as a function of the phenology, biomass and light environment of each <strong>crop</strong> and weed<br />

plant on a daily timescale (Gardarin et al., 2007a). However, the temporally exten<strong>de</strong>d<br />

competition in PFCs as well as the repeated cuttings and regrowth events may produce weed<br />

plants that may differ in morphology compared to weed plants grown in annual <strong>crop</strong>s, which<br />

needs to be quantified by future studies and integrated in the current mo<strong>de</strong>l.<br />

B, the amount of ‘carbohydrate resources that can be remobilized for regrowth’, might be a<br />

function of i) the weed species (functional group), ii) the plant age, iii) the plant biomass<br />

before cutting, iv) the number of times and frequency the plant has previously been cut, and v)<br />

external conditions such as the temperature <strong>de</strong>termining the rate of biochemical processes.<br />

Although previous experiments <strong>de</strong>termined the absolute quantity of carbohydrates in plant<br />

roots and stubbles (Klimes and Klimesova, 2002; Rodriguez et al., 2007), the ‘quantity of<br />

carbohydrate that can be remobilized for regrowth’ (B) cannot directly be measured.<br />

However, it may be implemented as a ‘theoretical variable’ in the mo<strong>de</strong>l. According to the<br />

experimental results on several weed species, this variable would be:<br />

• negatively related to the plant age (Fig. 6 of Bonnot, 2008 and Fig. 4 of Article 4),<br />

• positively related to the plant biomass before cutting for plants of the same age (Table 4 of<br />

Henriot, 2007; Fig. 4 of Bonnot, 2008 and Fig. 3 of Article 4) [the belowground biomass is<br />

approximated by the aboveground biomass, which is possible as both are often closely<br />

related (Gedroc et al., 1996; Wardle et al., 2004)],<br />

• negatively related to the number of previous cuttings (Fig. 2 of Article 4), and<br />

• different between plant species functional groups (e.g. higher for perennials compared to<br />

annuals, Article 4).<br />

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