Relational contracts as a foundation for contractual incompleteness

Contractual incompleteness is generally defined by a trade-off between costs and benefits. We examine this trade-off in a dynamic setting and show how the ability of the parties to sustain a relational contract leads to more incomplete contracts.Contractual incompleteness, Relational Contract, Reputation, Repeated Games

Bureaucracy, Collegiality and Public Decision Making: the Case of Eighteenth Century France

One of the most debated questions in the literature on modern bureaucracies is whether their formal, impersonal rules of decision endow them (rightly or not) with a specific autonomy vis‐à‐vis special interests. We study the case of the Bureau de Commerce, a small, modernizing agency within the illiberal Ancien Régime French monarchy, in charge i.a. of supporting private entrepreneurs. Decision making was founded on the articulation between a vertical administrative organization aimed at collecting information and consulting stakeholders, and two colleges of experts, which discussed cases on a consensual, peers’ basis. We ask whether the relative openness of this procedure led to outright capture by outside rent‐seeking interests, or whether the Bureau could balance them and reach relatively autonomous and consistent decisions. We analyzed how it handled and decided 246 submissions for privileges, or rents, made between 1724 and 1740. We show that the decision to reject, accept entirely or curtail individual submissions was shaped within the administrative procedure – rather than by cliques and clienteles. Each main and competing voice had a significant though differentiated impact on outcomes; and substantive arguments, for or against each application, also had a specific impact

Biological systems: from water radiolysis to carbon ion radiotherapy

International audienceHadron therapy is an innovative cancer treatment method based on the acceleration of light ions at high energy. In addition to their interesting profile of dose deposition, which ensures accurate targeting of localized tumors, carbon ions offer biological properties that lead to an efficient treatment for radio-and chemo-resistant tumors and to provide a boost for tumors in hypoxia. This paper is a short review of the progress in theoretical, experimental, fundamental and applied research, aiming at understanding the origin of the biological benefits of light ions better. As a limit of such a vast and multidisciplinary domain, this review adopts the point of view of the physicists, leaning on results obtained in connection with CIMAP's IRRABAT platform. 1. Introduction Interaction of fast ions with biological systems constitutes one aspect of the interdisciplinary researches performed with ion-beam facilities. This domain is as rich as it is complex since it encompasses several orders of magnitude in both space and time. The shortest space and time scale corresponds to atomic collisions, which may be as short as 10 −18 s for the interaction of fast ions with individual atoms. At the opposite end of this domain, late effects – like cancer induction, chromosomal instability or organ dysfunctions – may appear or remain several years after irradiations. While irradiations may be limited to a very localized region, the whole behavior of an organ may be affected, possibly leading to human death, in particular when the irradiation dose and spatial extension are high. Between these two extreme scales, stands a great number of mechanisms, including for instance: the transport of the primary ejected electrons, the relaxation of the ionized and excited molecules, which may lead to direct damage in biological targets and to radical species and associated biochemical reactions. These early physical and chemical stages are followed by numerous and complex cell responses, such as the triggering of mechanisms to check DNA, to repair its damage, to manage the oxidative stress or to induce cell death. The numerous biological endpoints that have been studied reveal the complexity and the diversity of this biological response. These endpoints may involve particular structures of cells at the molecular scale (tracking of protein activities, damage in DNA, protein or lipid) or at the sub-cellular scale (chromosomes, nucleus, membranes, mitochondria.. .) and may concern cell organization (3D cell culture, tissues, organs, body). The domain of low dose

Doing It by the Book: Political Contestability and Public Contract Renegotiations

We present a public procurement model in which contractual flexibility and political tolerance for contractual deviations determine renegotiations. In the model, contractual flexibility allows for adaptation without formal renegotiation, while political tolerance for deviations decreases with political competition. We then compare renegotiation rates of procurement contracts in which the procurer is either a public administration or a private corporation. We find robust evidence consistent with the model predictions: public-to- private contracts are renegotiated more often than comparable private-to-private contracts, and that this pattern is more salient in politically contestable jurisdictions. The frequent renegotiation of public contracts results from their inherent rigidity and provides a relational quality of adaptability to contingencies in politically contestable environments

A chest wall model based on rib kinematics

International audienceThe success of radiotherapy treatment could be compromised by motion. Lung tumours are particularly concerned by this problem because their positions are subject to breathing motion. To reduce the uncertainty on the position of pulmonary tumours during breathing cycle, we propose to develop a complete thoracic biomechanical model. This model will be monitored through the measurement of external parameters (thorax outer-surface motion, air flow...) and should predict in real-time the location of lung tumour. In this paper, we expose a biomechanical model of the lung environment, based on anatomical and physiological knowledge. The model includes the skin, the ribs, the pleura and the soft tissue between the skin and the ribcage. Motions and deformations are computed with the Finite Element Method. The ribcage direct kinematics model, permits to compute the skin position from the ribs motion. Conversely, the inverse kinematics provides rib motion and consequently lung motion. It can be computed from the outer-surface motion. With regards to available clinical data the results are promising. In particular, the average error is lower than the resolution of the CT-scan images used as input data.Le succès du traitement par radiothérapie pourrait être compromis par le mouvement. Les tumeurs pulmonaires sont particulièrement concernées par ce problème, parce que leurs positions sont soumises à la respiration. Pour réduire l'incertitude sur la position des tumeurs pulmonaires au cours de la respiration, nous proposons de développer un modèle biomécanique de la cage thoracique. Ce modèle sera suivi par la mesure des paramètres externes (mouvement de la surface du thorax extérieur, quantité d'air inspirée et expirée ...) et devrait prévoir en temps réel la localisation de la tumeur du poumon. Dans ce document, nous exposons un modèle biomécanique de l'appareil respiratoire, fondé sur les connaissances anatomiques et physiologiques. Le modèle comprend la peau, les côtes, la plèvre et les tissus mous entre la peau et la cage thoracique. Les mouvements et les déformations sont calculées avec la méthode des éléments finis. Le modèle cinématique direct de la cage thoracique permet de calculer la position de la peau à partir du mouvement des côtes. Inversement, la cinématique inverse permet de déduire le mouvement des côtes et des poumons à partir du mouvement externe de la peau. Les résultats obtenus par ce modèle sont satisfaisants surtout que l’erreur moyenne est inférieure à la résolution des images CT-scan utilisées comme données d’entrée

A Preliminary Study For A Biomechanical Model Of The Respiratory System

Engineering and Computational Sciences for Medical Imaging in Oncology - ECSMIO is the special session 1 of International Conference on Computer Vision Theory and Applications - VISAPP 2010International audienceTumour motion is an essential source of error for treatment planning in radiation therapy. This motion is mostly due to patient respiration. To account for tumour motion, we propose a solution that is based on the biomechanical modelling of the respiratory system. To compute deformations and displacements, we use continuous mechanics laws solved with the finite element method. In this paper, we propose a preliminary study of a complete model of the respiratory system including lungs, chest wall and a simple model of the diaphragm. This feasibility study is achieved by using the data of a "virtual patient". Results are in accordance with the anatomic reality, showing the feasibility of a complete model of the respiratory system

Virus preparations from the mixed-infected P70 Pinot Noir accession exhibit GLRaV-1/GVA ‘end-to-end’ particles

P70 is a Pinot Noir grapevine accession that displays strong leafroll disease symptoms. A high-throughput sequencing (HTS)-based analysis established that P70 was mixed-infected by two variants of grapevine leafroll-associated virus 1 (GLRaV-1, genus Ampelovirus) and one of grapevine virus A (GVA, genus Vitivirus) as well as by two viroids (hop stunt viroid [HSVd] and grapevine yellow speckle viroid 1 [GYSVd1]) and four variants of grapevine rupestris stem pitting-associated virus (GRSPaV). Immunogold labelling using gold particles of two different diameters revealed the existence of ‘hybrid’ particles labelled at one end as GLRaV-1, with the rest labelled as GVA. In this work, we suggest that immunogold labelling can provide information about the biology of the viruses, going deeper than just genomic information provided by HTS, from which no recombinant or ‘chimeric’ GLRaV-1/GVA sequences had been identified in the dataset. Our observations suggest an unknown interaction between members of two different viral species that are often encountered together in a single grapevine, highlighting potential consequences in the vector biology and epidemiology of leafroll and rugose-wood diseases