4 research outputs found

    Patterns of ash (Fraxinus excelsior L.) colonization in mountain grasslands: the importance of management practices

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    International audienceWoody colonization of grasslands is often associated with changes in abiotic or biotic conditions or a combination of both. Widely used as fodder and litter in the past traditional agro-pastoral system, ash (Fraxinus excelsior L.) has now become a colonizing species of mountain grasslands in the French Pyrenees. Its present distribution is dependent on past human activities and it is locally controlled by propagule pressure and abiotic conditions. However, even when all favourable conditions are met, all the potentially colonizable grasslands are not invaded. We hypothesize that management practices should play a crucial role in the control of ash colonization. From empirical field surveys we have compared the botanical composition of a set of grasslands (present and former) differing in management practices and level of ash colonization. We have displayed a kind of successional gradient positively linked to both ash cover and height but not to the age of trees. We have tested the relationships between ash presence in grassland and management types i.e. cutting and/or grazing, management intensity and some grassland communities' features i.e. total and local specific richness and species heterogeneity. Mixed use (cutting and grazing) is negatively linked to ash presence in grassland whereas grazing alone positively. Mixed use and high grazing intensity are directly preventing ash seedlings establishment, when low grazing intensity is allowing ash seedlings establishment indirectly through herbaceous vegetation neglected by livestock. Our results show the existence of a limit between grasslands with and without established ashes corresponding to a threshold in the intensity of use. Under this threshold, when ash is established, the colonization process seems to become irreversible. Ash possesses the ability of compensatory growth and therefore under a high grazing intensity develops a subterranean vegetative reproduction. However the question remains at which stage of seedling development and grazing intensity these strategies could occur

    Stem growth of woody species at the Nkuhlu exclosures, Kruger National Park: 2006–2010

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    An important aspect of managing African conservation areas involves understanding how large herbivores affect woody plant growth. Yet, data on growth rates of woody species in savannas are scarce, despite its critical importance for developing models to guide ecosystem management. What effect do browsing and season have on woody stem growth? Assuming no growth happens in the dry season, browsing should reduce stem growth in the wet season only. Secondly, do functional species groups differ in stem growth? For example, assuming fine-leaved, spiny species’ growth is not compromised by carbon-based chemical defences, they should grow faster than broad-leaved, chemically defended species. Dendrometers were fixed at 20 cm in height on the main stems of 244 random plants of six woody species in three plots (all large herbivores excluded, partial exclusion, and control) and observed from late 2006 to early 2010. Average monthly increment (AMI) per dendrometer and season (dry, wet) was calculated and the interaction between plot and season tested per species, controlling for initial stem girth. AMIs of Combretum apiculatum, Dichrostachys cinerea and Grewia flavescens were zero in the dry season, whilst those of Acacia exuvialis, Acacia grandicornuta and Euclea divinorum were either positive or negative in the dry season. Wet-season AMI of D. cinerea and dry-season AMI of G. flavescens tended to be reduced by browser exclusion. Net AMI (sum of the seasonal AMIs) was tested per species, but results suggested that only D. cinerea tended to be affected by browser exclusion. The results also suggested that stem radial growth of some fast-growing species is more prone to reduction by browser exclusion than the growth of other species, potentially reducing their competitiveness and increasing their risk of extirpation. Finally, the usefulness of grouping woody species into simple functional groups (e.g. fine-leaved vs. broad-leaved) for ecosystem management purposes in savannas requires further consideration. Conservation implications: Growth rates of woody plants are important parameters in savanna models, but data are scarce. Monitoring dendrometers in manipulative situations over several years can help fill that gap. Results of such studies can be used to identify species prone to high risk of extirpation
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