Phytoextraction represents an innovative approach in the management of nickel (Ni) rich soils whether natural (ultramafic) or anthropogenic (contaminated sites). However, its success depends both on the production of a high plant biomass and the ability of plants to accumulate metals. The application of nitrogen (N) fertilizer can improve the biological and chemical soil fertility and thus agricultural yields. Moreover, soil microorganisms play a key role by influencing nutrient flows, which are the main limiting factors of plant growth in degraded soils. In this work, we investigated the effects of two levels of both Ni and mineral N soil applications on the microbial activities and Ni phytoextraction efficiency by Alyssum murale growing in a pot experiment during 5 months. Plant growth, nutrients and Ni uptake, soil microbial populations and their enzymatic activities involved in the biogeochemical cycles of nitrogen, phosphorus, carbon and sulfur (urease, alkaline phosphatase, β‐glucosidase and arylsulfatase, respectively) were determined. The results showed that plant dry mass was unsurprisingly not affected when the soil Ni concentration was increased. However, it led to an increase of the amount of Ni extracted per pot. A negative effect of Ni addition was observed on both total bacteria and urease activity, without any effect on other enzymes. On the contrary, N fertilizer played a significant positive role by promoting both plant growth and Ni phytoextraction, partly as a result of the stimulation and flourishing of bacterial populations.
Invertebrates have a diverse immune system that responds differently to stressors such as pesticides and pathogens, which leads to different degrees of susceptibility. Honeybees are facing a phenomenon called colony collapse disorder which is attributed to several factors including pesticides and pathogens. We applied an in vitro approach to assess the response of immune-activated hemocytes from Apis mellifera, Drosophila melanogaster and Mamestra brassicae after exposure to imidacloprid and amitraz. Hemocytes were exposed to the pesticides in single and co-exposures using zymosan A for immune activation. We measured the effect of these exposures on cell viability, nitric oxide (NO) production from 15 to 120 min and on extracellular hydrogen peroxide (H2O2) production after 3 h to assess potential alterations in the oxidative response. Our results indicate that NO and H2O2 production is more altered in honeybee hemocytes compared to D. melanogaster and M. brassicae cell lines. There is also a differential production at different time points after pesticide exposure between these insect species as contrasting effects were evident with the oxidative responses in hemocytes. The results imply that imidacloprid and amitraz act differently on the immune response among insect orders and may render honeybee colonies more susceptible to infection and pests.
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