Adding a diversity of legumes to a crop decision-support system: Maintaining satisfactory accuracy while keeping the model simple

International audienceIn a context of economic and environmental concerns in agriculture, legumes appear to be suitable alternative crops to diversify current cropping systems and reduce their dependence on synthetic nitrogen (N) fertiliser and protein from imported soya bean. However, legume-based cropping systems may increase N losses through nitrate leaching if the N available from legumes does not coincide with subsequent crop requirements. To help agricultural advisers manage N in these systems, we adapted the decision-support system Syst’N®, designed to assess N losses in cropping systems, to simulate three annual and one perennial legume crops: pea, faba bean, soya bean and lucerne. To this end, we adapted and simplified existing submodels of legume functioning to include them in Syst’N, to keep the latter simple. We adapted the submodels “BNF” (i.e. biological N fixation) from the STICS model and “dormancy” from the CropSyst model. We also added the ability to enter the flowering date to improve predictions (improvement in N fixation’s rRMSE from 57% to 41% and EF from 0.57 to 0.77). The equations and associated parameter set developed for the four legume crops yielded satisfying predictions of crop biomass (rMBE = 9%, EF = 0.82, rRMSE = 39%) and N content (rMBE = 5%, EF = 0.76, rRMSE = 37%). These performances support the philosophy of Syst’N® that requires minimising the number of additional parameters for users when representing new crops or processes

Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?

International audienceObjective: Uniparental disomy (UPD) testing is currently recommended during pregnancy in fetuses carrying a balanced Robertsonian translocation (ROB) involving chromosome 14 or 15, both chromosomes containing imprinted genes. The overall risk that such a fetus presents a UPD has been previously estimated to be around ~0.6‐0.8%. However, because UPD are rare events and this estimate has been calculated from a number of studies of limited size, we have reevaluated the risk of UPD in fetuses for whom one of the parents was known to carry a nonhomologous ROB (NHROB).Method: We focused our multicentric study on NHROB involving chromosome 14 and/or 15. A total of 1747 UPD testing were performed in fetuses during pregnancy for the presence of UPD(14) and/or UPD(15).Result: All fetuses were negative except one with a UPD(14) associated with a maternally inherited rob(13;14).Conclusion: Considering these data, the risk of UPD following prenatal diagnosis of an inherited ROB involving chromosome 14 and/or 15 could be estimated to be around 0.06%, far less than the previous estimation. Importantly, the risk of miscarriage following an invasive prenatal sampling is higher than the risk of UPD. Therefore, we do not recommend prenatal testing for UPD for these pregnancies and parents should be reassured