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Selection of resistant upland cotton genotypes challenged with aggressive isolates of Meloidogyne incognita race 3

Received: July 11th, 2022 ; Accepted: August 19th, 2022 ; Published: August 25th, 2022 ; Correspondence: [email protected] study aimed to select populations of M. incognita race 3 for screening cotton genotypes as part of a breeding program for the development of resistant cotton cultivars. Five isolates of M. incognita race 3, collected in Western Paraná, Brazil, were tested for virulence and aggressiveness against the cotton cultivars FM966 (susceptible), IAC 24 (resistant), CD 409, and FMT 701 (moderately resistants) under greenhouse conditions, and following a factorial design with five replicates. Thirty-one cotton genotypes were screened against the three most aggressive isolates of M. incognita race 3 tested before and kept under greenhouse conditions following a factorial design with five replicates. Experiments run under greenhouse conditions had single cotton plants inoculated with 5,000 eggs/J2 of M. incognita and were assessed at 120 days after inoculation considering the variables gall index, egg mass index, total eggs, and reproduction factor. The same genotypes tested under greenhouse conditions were also grown in a field infested with M. incognita race 3 in a randomized block design with 10 replicates. In the field, the M. incognita population was monitored by the quantification of J2 forms in soil samples collected before sowing, 60 days after sowing (DAS), and 120 DAS. A gall index score was used to evaluate the roots of cotton genotypes at 120 DAS. The isolate from Umuarama was the most aggressive, followed by Moreira Sales and Iporã. The genotypes CD 05-419, CD 05-945, CD 05-1087, and CD 05-1170 showed resistance against M. incognita race 3 under greenhouse and field conditions

Performance of two formal tests based on martingales residuals to check the proportional hazard assumption and the functional form of the prognostic factors in flexible parametric excess hazard models.

: Net survival, the one that would be observed if the disease under study was the only cause of death, is an important, useful, and increasingly used indicator in public health, especially in population-based studies. Estimates of net survival and effects of prognostic factor can be obtained by excess hazard regression modeling. Whereas various diagnostic tools were developed for overall survival analysis, few methods are available to check the assumptions of excess hazard models. We propose here two formal tests to check the proportional hazard assumption and the validity of the functional form of the covariate effects in the context of flexible parametric excess hazard modeling. These tests were adapted from martingale residual-based tests for parametric modeling of overall survival to allow adding to the model a necessary element for net survival analysis: the population mortality hazard. We studied the size and the power of these tests through an extensive simulation study based on complex but realistic data. The new tests showed sizes close to the nominal values and satisfactory powers. The power of the proportionality test was similar or greater than that of other tests already available in the field of net survival. We illustrate the use of these tests with real data from French cancer registries.<br/

Can Observers Predict Trustworthiness?

We investigate whether experimental subjects can predict behavior in a prisoner's dilemma played on a TV show. Subjects report probabilistic beliefs that a player cooperates, before and after the players communicate. Subjects correctly predict that women and players who make a voluntary promise are more likely to cooperate. They are able to distinguish truth from lies when a player is asked about her intentions by the host. Subjects are to some extent able to predict behavior; their beliefs are 7~percentage points higher for cooperators than for defectors. We also study their Bayesian updating. Beliefs do not satisfy the martingale property and display mean reversion

Background-Independence

Intuitively speaking, a classical field theory is background-independent if the structure required to make sense of its equations is itself subject to dynamical evolution, rather than being imposed ab initio. The aim of this paper is to provide an explication of this intuitive notion. Background-independence is not a not formal property of theories: the question whether a theory is background-independent depends upon how the theory is interpreted. Under the approach proposed here, a theory is fully background-independent relative to an interpretation if each physical possibility corresponds to a distinct spacetime geometry; and it falls short of full background-independence to the extent that this condition fails.Comment: Forthcoming in General Relativity and Gravitatio

Pseudohypoaldosteronisms, report on a 10-patient series

Background. Type 1 pseudohypoaldosteronism (PHA1) is a salt-wasting syndrome caused by mineralocorticoid resistance. Autosomal recessive and dominant hereditary forms are caused by Epithelial Na Channel and Mineralocorticoid Receptor mutation respectively, while secondary PHA1 is usually associated with urological problems. Methods. Ten patients were studied in four French pediatric units in order to characterize PHA1 spectrum in infants. Patients were selected by chart review. Genetic, clinical and biochemistry data were collected and analyzed. Results. Autosomal recessive PHA1 (n = 3) was diagnosed at 6 and 7 days of life in three patients presenting with severe hyperkalaemia and weight loss. After 8 months, 3 and 5 years on follow-up, neurological development and longitudinal growth was normal with high sodium supplementation. Autosomal dominant PHA1 (n = 4) was revealed at 15, 19, 22 and 30 days of life because of failure to thrive. At 8 months, 3 and 21 years of age, longitudinal growth was normal in three patients who were given salt supplementation; no significant catch-up growth was obtained in the last patient at 20 months of age. Secondary PHA1 (n = 3) was diagnosed at 11, 26 days and 5 months of life concomitantly with acute pyelonephritis in three children with either renal hypoplasia, urinary duplication or bilateral megaureter. The outcome was favourable and salt supplementation was discontinued after 3, 11 and 13 months. Conclusions. PHA1 should be suspected in case of severe hyperkalemia and weight loss in infants and need careful management. Pathogenesis of secondary PHA1 is still challenging and further studies are mandatory to highlight the link between infection, developing urinary tract and pseudohypoaldosteronis