Comparing LUCAS Soil and national systems: Towards a harmonized European Soil monitoring network

17 Pág.A recent assessment states that 60–70% of soils in Europe are considered degraded. Protecting such valuable resource require knowledge on soil status through monitoring systems. In Europe, different types of monitoring networks currently exist in parallel. Many EU Member states (MS) developed their own national soil information monitoring system (N-SIMS), some being in place for decades. In parallel in 2009, the European Commission extended the periodic Land Use/Land Cover Area Frame Survey (LUCAS) led by EUROSTAT to sample and analyse the main properties of topsoil in EU in order to develop a homogeneous dataset for EU. Both sources of information are needed to support European policies on soil health evaluation. However, a question remains whether the assessment obtained by using soil properties from both monitoring programs (N-SIMS and LUCAS Soil) are comparable, and what could be the limitations of using either one dataset or the other. Conducted in the context of European Joint Programme (EJP) SOIL, this study shows the results of a comparison between N-SIMS and LUCAS Soil programs among 12 different EU member states including BE, DE, DK, EE, ES, FR, DE, HU, IT, NL, PL, SE and SK. The comparison was done on: (i) the sampling strategies including site densities, land cover and soil type distribution; (ii) the statistical distribution of three soil properties (organic carbon, pH and clay content); (iii) two potential indicators of soil quality (i.e. OC/Clay ratio and pH classes). The results underlined substantial differences in soil properties statistical distributions between N-SIMS and LUCAS Soil in many member states, particularly for woodland and grassland soils, affecting the evaluation of soil health using indicators. Such differences might be explained by both the monitoring strategy and sampling or analytical protocols exposing the potential effect of data source on European and national policies. The results demonstrate the need to work towards data harmonization and in the light of the Soil Monitoring Law, to carefully design the future of soil monitoring in Europe taking into account both LUCAS Soil and N-SIMS considering the significant impact of the monitoring strategies and protocols on soil health indicators.This work was financed by the H2020 grant agreement number of EJPSOIL, H2020 GA number 862695.Peer reviewe

GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling

Growth factor signaling results in dramatic phenotypic changes in cells, which require commensurate alterations in cellular metabolism. Mutations in SLC2A10/GLUT10, a member of the facilitative glucose transporter family, are associated with altered transforming growth factor- (TGF) signaling in patients with arterial tortuosity syndrome (ATS). The objective of this work was to test whether SLC2A10/GLUT10 can serve as a link between TGF-related transcriptional regulation and metabolism during development. In zebrafish embryos, knockdown of slc2a10 using antisense morpholino oligonucleotide injection caused a wavy notochord and cardiovascular abnormalities with a reduced heart rate and blood flow, which was coupled with an incomplete and irregular vascular patterning. This was phenocopied by treatment with a small-molecule inhibitor of TGF receptor (tgfbr1/alk5). Array hybridization showed that the changes at the transcriptome level caused by the two treatments were highly correlated, revealing that a reduced tgfbr1 signaling is a key feature of ATS in early zebrafish development. Interestingly, a large proportion of the genes, which were specifically dysregulated after glut10 depletion gene and not by tgfbr1 inhibition, play a major role in mitochondrial function. Consistent with these results, slc2a10 morphants showed decreased respiration and reduced TGF reporter gene activity. Finally, co-injection of antisense morpholinos targeting slc2a10 and smad7 (a TGF inhibitor) resulted in a partial rescue of smad7 morphant phenotypes, suggesting scl2a10/glut10 functions downstream of smads. Taken together, glut10 is essential for cardiovascular development by facilitating both mitochondrial respiration and TGF signaling