A Statistical Model to Explain the Mendel--Fisher Controversy

In 1866 Gregor Mendel published a seminal paper containing the foundations of modern genetics. In 1936 Ronald Fisher published a statistical analysis of Mendel's data concluding that "the data of most, if not all, of the experiments have been falsified so as to agree closely with Mendel's expectations." The accusation gave rise to a controversy which has reached the present time. There are reasonable grounds to assume that a certain unconscious bias was systematically introduced in Mendel's experimentation. Based on this assumption, a probability model that fits Mendel's data and does not offend Fisher's analysis is given. This reconciliation model may well be the end of the Mendel--Fisher controversy.Comment: Published in at http://dx.doi.org/10.1214/10-STS342 the Statistical Science (http://www.imstat.org/sts/) by the Institute of Mathematical Statistics (http://www.imstat.org

Optimal diffusion in ecological dynamics with Allee effect in a metapopulation

How diffusion impacts on ecological dynamics under the Allee effect and spatial constraints? That is the question we address. Employing a microscopic minimal model in a metapopulation (without imposing nonlinear birth and death rates) we evince --- both numerically and analitically --- the emergence of an optimal diffusion that maximises the survival probability. Even though, at first such result seems counter-intuitive, it has empirical support from recent experiments with engineered bacteria. Moreover, we show that this optimal diffusion disappears for loose spatial constraints.Comment: 16 pages; 6 figure

Piecewise contractions defined by iterated function systems

Let $\phi_1,\ldots,\phi_n:[0,1]\to (0,1)$ be Lipschitz contractions. Let $I=[0,1)$, $x_0=0$ and $x_n=1$. We prove that for Lebesgue almost every $(x_1,...,x_{n-1})$ satisfying $0<x_1<\cdots <x_{n-1}<1$, the piecewise contraction $f:I\to I$ defined by $x\in [x_{i-1},x_i)\mapsto \phi_i(x)$ is asymptotically periodic. More precisely, $f$ has at least one and at most $n$ periodic orbits and the $\omega$-limit set $\omega_f(x)$ is a periodic orbit of $f$ for every $x\in I$.Comment: 16 pages, two figure

Asymptotically periodic piecewise contractions of the interval

We consider the iterates of a generic injective piecewise contraction of the interval defined by a finite family of contractions. Let $\phi_i:[0,1]\to (0,1)$, $1\le i\le n$, be $C^2$-diffeomorphisms with $\sup_{x\in (0,1)} \vert D\phi_i(x)\vert<1$ whose images $\phi_1([0,1]), \ldots, \phi_n([0,1])$ are pairwise disjoint. Let $0<x_1<\cdots<x_{n-1}<1$ and let $I_1,\ldots, I_n$ be a partition of the interval $[0,1)$ into subintervals $I_i$ having interior $(x_{i-1},x_i)$, where $x_0=0$ and $x_n=1$. Let $f_{x_1,\ldots,x_{n-1}}$ be the map given by $x\mapsto \phi_i(x)$ if $x\in I_i$, for $1\le i\le n$. Among other results we prove that for Lebesgue almost every $(x_1,\ldots,x_{n-1})$, the piecewise contraction $f_{x_1,\ldots,x_{n-1}}$ is asymptotically periodic.Comment: 8 page

Invisible Z decay width bounds on active-sterile neutrino mixing in the (3+1) and (3+2) models

In this work we consider the standard model extended with singlet sterile neutrinos with mass in the eV range and mixed with the active neutrinos. The active-sterile neutrino mixing renders new contributions to the invisible Z decay width which, in the case of light sterile neutrinos, depends on the active-sterile mixing matrix elements only. We then use the current experimental value of the invisible Z decay width to obtain bounds on these mixing matrix elements for both (3+1) and (3+2) models.Comment: 10 pages, 5 figure

Aromatic Plants in Eurasian Blue Tit Nests: The ‘Nest

The ‘Nest Protection Hypothesis’ suggests that some birds add aromatic plants to their nests to repel or kill ectoparasites. This behavior has been described for several species, including the Eurasian Blue Tit (Cyanistes caeruleus). We studied the reproductive performance, based on 26 nests (in nest boxes), of this species in mixed forested areas of Quercus spp. and Pinus pinea in the Parque Florestal de Monsanto, the largest park of Lisbon, Portugal. The frequency of aromatic plants in nests was compared with frequency of these plants in the study area. The three most frequent aromatic plants (Dittrichia viscosa, Lavandula dentata, Calamintha baetica) in nests were used more than expected from their availability in the study area. We could not reject the null hypothesis that nest survival rate is independent of the presence of aromatic plants in the nest