Changes in land use strongly influence habitat attributes (e.g., herbaceous ground cover and tree richness) and can consequently affect ecological functions. Most studies have focused on the response of these ecological functions to land-use changes within only a single vegetation type. These studies have often focused solely on agricultural conversion of forests, making it nearly impossible to draw general conclusions across other vegetation types or with other land-use changes (e.g., afforestation). We examined the consequences of agricultural conversion for seed removal by ants in native grassland, savanna, and savanna-forest habitats that had been transformed to planted pastures (Brachiaria decumbens) and tree plantations (Eucalyptus spp.) and explored if changes in seed removal were correlated with differences in habitat attributes between habitat types. We found that land-use changes affected seed removal across the tree cover gradient and that the magnitude of impact was influenced by similarity in habitat attributes between native and converted habitats, being greater where there was afforestation (Eucalyptus spp in grassland and savanna). Herbaceous ground cover, soil hardness, and tree richness were the most important habitat attributes that correlated with differences in seed removal. Our results reveal that the magnitude of impact of land-use changes on seed removal varies depending on native vegetation type and is associated with the type of habitat attribute change. Our findings have implications for biodiversity in tropical grassy systems: afforestation can have a greater detrimental impact on ecological function than tree loss.
There has been an increase in the number of studies using seed removal by ants to evaluate ecosystem functioning; however, these studies encompassed varying time periods and used different types of seeds. Therefore, our aim was to evaluate differences in the proportion of seeds removed by ants in impacted and non-impacted sites in Brazilian savanna. Furthermore, we evaluated seed removal (1) during the morning and after a 24h period of seed exposure and (2) using natural and artificial seeds (manipulated resource to resemble natural seeds). The proportion of seeds removed was higher after the 24h exposure period (artificial seeds) regardless of site status, and more artificial seeds were removed than natural seeds. Our recommendations regarding sampling period depend on whether evaluating impacted or non-impacted sites. Although seed removal was greater after 24h in both impacted and non-impacted sites, we suggest that research evaluating the proportion of seeds removed in non-impacted sites should be performed only in the morning period to optimize the sampling time (removal of 60% during this period). When the aim is to compare non-impacted and impacted sites, we suggest evaluating after 24h of exposure, since the impacted sites experienced a higher proportion of seed removal during the afternoon and/or night time periods. Furthermore, we recommend the use of artificial seeds because they are easier to obtain and manipulate, and allow us to do comparisons between studies at different regions. We consider these findings an important first step towards standardizing future research on seed removal in Brazilian savannas by facilitating fieldwork and allowing comparisons to be made among different studies.
Ant-aphid interactions may affect host plants in several ways, however, most studies measure only the amount of fruit and seed produced, and do not test seed viability. Therefore, the aim of this study was to assess the effects of the presence of ant-aphid interactions upon host plant productivity and seed viability in two different contexts: isolated and within an arthropod community. For this purpose we tested the hypothesis that in both isolated and community contexts, the presence of an ant-aphid interaction will have a positive effect on fruit and seed production, seed biomass and rate of seed germination, and a negative effect on abnormal seedling rates, in comparison to plants without ants. We performed a field mesocosm experiment containing five treatments: Ant-aphid, Aphid, Community, Ant-free community and Control. We counted fruits and seeds produced by each treatment, and conducted experiments for seed biomass and germinability. We found that in the community context the presence of an ant-aphid interaction negatively affected fruit and seed production. We think this may be because aphid attendance by tending-ants promotes aphid damage to the host plant, but without an affect on seed weight and viability. On the other hand, when isolated, the presence of an ant-aphid interaction positively affected fruit and seed production. These positive effects are related to the cleaning services offered to aphids by tending-ants, which prevent the development of saprophytic fungi on the surface of leaves, which would cause a decrease in photosynthetic rates. Our study is important because we evaluated some parameters of plant fitness that have not been addressed very well by other studies involving the effects of ant-aphid interactions mainly on plants with short life cycles. Lastly, our context dependent approach sheds new light on how ecological interactions can vary among different methods of crop management.
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