Diversifying crop rotations with temporary grasslands - Université de ...
Diversifying crop rotations with temporary grasslands - Université de ...
Diversifying crop rotations with temporary grasslands - Université de ...
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higher weed seed losses (e.g., Menalled et al., 2000; Gallandt et<br />
al., 2005; Holmes and Froud-Williams, 2005; Mauchline et al.,<br />
2005). Yet, some authors have reported methodological biases in<br />
the assessment of the relative impact of seed predator guilds. Some<br />
predators may avoid the exclusion cages even though their body<br />
size would permit them to pass through the mesh openings. Smaller<br />
invertebrates might also be unable to remove the seeds glued to the<br />
sandpaper cards (Shuler et al., 2008). However, possible un<strong>de</strong>restimations<br />
of both the total predation rates and the contribution<br />
of invertebrates in this study would be systematic and would not<br />
challenge the comparisons between the treatments.<br />
4.1. Vegetation cover<br />
The impact of vegetation cover was nearly always positive<br />
among the trials, weed species, and exclusion treatments (Table 2).<br />
Positive impacts of vegetation cover were in line <strong>with</strong> most of the<br />
previous studies conducted in intensively managed and more natural<br />
ecosystems in various locations (Table 1). In our study, about<br />
12% of the variation in seed predation rates could be explained by<br />
vegetation cover and this value was above 30% when global predation<br />
rates were high. Similar rates were observed by Heggenstaller<br />
et al. (2006). Vegetation cover was thus probably a major factor<br />
affecting weed seed predation rates.<br />
Vegetation cover may change the habitat quality for seed predators<br />
by modifying (a) the microclimate (light, temperature) and soil<br />
characteristics (humidity, plant litter), (b) the presence of alternative<br />
food items such as leaves or insect larvae, (c) the presence<br />
of living or <strong>de</strong>ad plant material that may be used as substrates<br />
for reproduction, and (d) the risk of being predated by carnivores<br />
(Manson and Stiles, 1998; Landis et al., 2005). Given this variety of<br />
possible mechanisms, it may be expected that different predator<br />
guilds react differently to the quantity (and quality) of vegetation<br />
cover. Several studies indicated that most granivorous beetles<br />
and ro<strong>de</strong>nts prefer <strong>de</strong>nser vegetation (Hulme, 1997; Manson and<br />
Stiles, 1998; Honek and Jarosik, 2000; Shearin et al., 2008), while<br />
granivorous birds and ants may prefer open patches (Hulme, 1997;<br />
Moorcroft et al., 2002; Butler et al., 2005). While most of the previous<br />
studies focused either on vertebrates or on invertebrates<br />
(Table 1), our exclusion treatments indicated that vegetation cover<br />
increased weed seed predation by both guilds, except for periods<br />
<strong>with</strong> very low predation rates. Field observations and pitfall<br />
trapping suggested that both mice and granivorous beetles were<br />
abundant in the experimental field, while ants were rarely captured<br />
(data not shown). There is also no reason to assume that predation<br />
rates would be always linearly related to vegetation cover.<br />
To our knowledge, the study by Navntoft et al. (2009) is the first<br />
one to report non-linear impacts of vegetation cover on weed seed<br />
predation (Table 1). In our study, some relationships were rather<br />
exponential, e.g., for predation by Invertebrates in July (Fig. 2).<br />
4.2. Crop species vs. cutting<br />
Heggenstaller et al. (2006) found that seed predation rates<br />
follow the seasonal <strong>crop</strong> biomass <strong>de</strong>velopment and would be<br />
temporarily reduced after mowing in perennial forage <strong>crop</strong>s. Our<br />
results based on simultaneous comparisons of cut and uncut plots<br />
(reducing potential confounding temporal effects) support this<br />
hypothesis. In uncut <strong>crop</strong>s, predation rates were higher in Medicago<br />
compared to Dactylis <strong>crop</strong>s. Several authors reported ten<strong>de</strong>ncies<br />
towards higher seed predation in legume <strong>crop</strong>s compared to nonlegume<br />
<strong>crop</strong>s (An<strong>de</strong>rsson, 1998; Gallandt et al., 2005; Heggenstaller<br />
et al., 2006), but the reason why predators might prefer legume<br />
<strong>crop</strong>s over grasses is still unclear.<br />
In our experiment, the greater explanatory power of cutting<br />
compared to <strong>crop</strong> species indicated that vegetation quantity<br />
H. Meiss et al. / Agriculture, Ecosystems and Environment 138 (2010) 10–16 15<br />
(biomass) was more important than vegetation quality, as already<br />
observed by Gallandt et al. (2005) for predation by invertebrates.<br />
The low predation rates observed on plots <strong>with</strong>out any vegetation<br />
agree <strong>with</strong> this hypothesis. Differences between the five treatments<br />
were mainly linked to the differences in cutting and to the complete<br />
absence of plants in bare soil plots. This was probably the reason<br />
why quite large parts of the variation between the treatments could<br />
also be explained by canopy light interception (Table 3). The use<br />
of continuous environmental variables instead of categorical factors<br />
has proved to be more successful in predicting other biological<br />
phenomena including species richness and spatial distributions of<br />
organisms (Lin<strong>de</strong>garth and Gamfeldt, 2005). In our case, the use<br />
of a continuous measurable variable allowed (i) reducing the number<br />
of parameters in the mo<strong>de</strong>ls (parsimony/Occam’s razor) and (ii)<br />
testing a more general hypothesis (“vegetation cover affects weed<br />
seed predation rates”) which may be helpful to <strong>de</strong>velop predictive<br />
mo<strong>de</strong>ls and facilitate the meta-analytical comparison of different<br />
studies (Lin<strong>de</strong>garth and Gamfeldt, 2005).<br />
Results suggested that weed seed predation may be enhanced<br />
by maintaining a high and temporally exten<strong>de</strong>d vegetation cover.<br />
Farmers may thus potentially favour the ecological service of weed<br />
seed predation by implementing <strong>crop</strong> management practices that<br />
maximize vegetation cover on arable fields. This might be achieved<br />
by using cover <strong>crop</strong>s, un<strong>de</strong>rsowing techniques, <strong>crop</strong> mixtures, or<br />
by including perennial <strong>crop</strong>s in the <strong>rotations</strong>.<br />
Acknowledgements<br />
We thank Florence Strbik, Cyril Naulin, François Duguet, Pascal<br />
Farcy, Philippe Chamoy and Denis Lapostolle for assistance in<br />
the field experiment; Fabrice Dessaint for statistical advice; Pavel<br />
Saska, Audrey Alignier, Aline Boursault, Richard Gunton and two<br />
anonymous reviewers for helpful comments on earlier versions<br />
of this manuscript. This work received funding from ECOGER and<br />
ADVHERB (ANR-08-STRA-02) projects, and AgroSupDijon. H. Meiss<br />
was granted a scholarship by the French Research Ministry.<br />
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