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

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Clay & Aguilar (1998) compared the weed seed banks, weed biomass and corn yields after (i)<br />

continuous corn or (ii) corn grown after 2-year-alfalfa stands <strong>with</strong> three fertilizer and<br />

herbici<strong>de</strong> input levels in South Dakota, USA. Alfalfa had positive impacts on corn yields and<br />

weed control, especially for the low and intermediate input systems.<br />

Schoofs & Entz (2000) compared the weed suppressive potential of five different spring<br />

see<strong>de</strong>d one-year forage <strong>crop</strong>s followed by a pea (Pisium sativum L.) test <strong>crop</strong>. All forage<br />

systems were at least as effective as a sprayed wheat (Triticum aestivum L.) control in<br />

suppressing Avena fatua L. and sometimes Setaria viridis L. Beauv. grass weeds; however,<br />

effects on broadleaved weeds were variable, especially for systems that did not provi<strong>de</strong><br />

season-long competition. In general, one-year forage <strong>crop</strong>s showed significant weed control<br />

benefits, but benefits of pluriannual forage <strong>crop</strong>s reported by the same research team (Entz et<br />

al., 1995) were stronger. The effectiveness of the different grain and forage <strong>crop</strong>s to reduce<br />

weed seed production ranked as following: fall rye (Secale cereale L.) (grain <strong>crop</strong>) > winter<br />

triticale (Triticosecale) (simulated grazing) > spring/winter triticale inter<strong>crop</strong> (silage, then<br />

simulated grazing) > sorghum-sudangrass (Sorghum bicolour [L.] Moench × Sorghum<br />

sudanese [Piper]) (hay) = alfalfa (hay) > spring triticale (silage) = weed fallow (silage) =<br />

sweet clover (Melilotus officinalis L.)/winter triticale double <strong>crop</strong> (hay, then simulated<br />

grazing) > wheat grain <strong>crop</strong>s <strong>with</strong> three different herbici<strong>de</strong> regimes.<br />

Sjursen (2001) monitored the <strong>de</strong>velopment of weed <strong>de</strong>nsities in the seed bank and the emerged<br />

vegetation in organic 6-year <strong>rotations</strong> including 3-year periods of perennial grass-clover leys<br />

and a sequence of three annual <strong>crop</strong>s. Seed <strong>de</strong>nsities of dicotyledonous weed species were<br />

highest after the 3 annual <strong>crop</strong>s (about 17600 seeds m -2 ) and lowest after the ley periods (7200<br />

seeds m -2<br />

), indicating a reduced seed input during the ley periods. In the emerged vegetation,<br />

species richness <strong>de</strong>creased from 19-20 during the annual <strong>crop</strong>s to 8 in the third year ley <strong>crop</strong><br />

while it remained constant in the seed bank (18-21 species). However, correlations between<br />

seed bank and emerged weed <strong>de</strong>nsities were rarely significant limiting the potential for<br />

predicting the actual weed vegetation.<br />

Cardina et al. (2002a) and Sosnoskie et al. (2006) compared the weed seed <strong>de</strong>nsity, diversity,<br />

and community composition between three <strong>crop</strong> <strong>rotations</strong>: continuous corn (CCC), cornsoybean<br />

(CS), corn-oat-hay (COH) and three tillage systems (conventional, minimum, and no-<br />

tillage) that were applied in two 35-year field experiments in Ohio, USA. Crop rotation was a<br />

more important <strong>de</strong>terminant of weed seed <strong>de</strong>nsity and species composition than tillage system.<br />

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