e+e−e^{+}e^{-} pairs from a nuclear transition signaling an elusive light neutral boson

Electron-positron pairs have been observed in the 10.95-MeV $0^-\to0^+$ decay in $^{16}$O. The branching ratio of the e$^+$e$^-$ pairs compared to the 3.84-MeV $0^-\to2^+$ $\gamma$ decay of the level is deduced to be $20(5)\times10^{-5}$. This magnetic monopole (M0) transition cannot proceed by $\gamma$-ray decay and is, to first order, forbidden for internal pair creation. However, the transition may also proceed by the emission of a light neutral $0^{-}$ or $1^{+}$ boson. Indeed, we do observe a sharp peak in the $e^{+}e^{-}$ angular correlation with all the characteristics belonging to the intermediate emission of such a boson with an invariant mass of 8.5(5) MeV/c$^2$. It may play a role in the current quest for light dark matter in the universe.Comment: 6 page

Observation of Anomalous Internal Pair Creation in 8^8Be: A Possible Signature of a Light, Neutral Boson

Electron-positron angular correlations were measured for the isovector magnetic dipole 17.6 MeV state ($J^\pi=1^+$, $T=1$) $\rightarrow$ ground state ($J^\pi=0^+$, $T=0$) and the isoscalar magnetic dipole 18.15 MeV ($J^\pi=1^+$, $T=0$) state $\rightarrow$ ground state transitions in $^{8}$Be. Significant deviation from the internal pair creation was observed at large angles in the angular correlation for the isoscalar transition with a confidence level of $> 5\sigma$. This observation might indicate that, in an intermediate step, a neutral isoscalar particle with a mass of 16.70$\pm0.35$ (stat)$\pm 0.5$ (sys) MeV$/c^2$ and $J^\pi = 1^+$ was created.Comment: 5 pages, 5 figure

Why do dogs (Canis familiaris) select the empty container in an observational learning task?

Many argue that dogs show unique susceptibility to human communicative signals that make them suitable for being engaged in complex co-operation with humans. It has also been revealed that socially provided information is particularly effective in influencing the behaviour of dogs even when the human’s action demonstration conveys inefficient or mistaken solution of task. It is unclear, however, how the communicative nature of the demonstration context and the presence of the human demonstrator affect the dogs’ object-choice behaviour in observational learning situations. In order to unfold the effects of these factors, 76 adult pet dogs could observe a communicative or a non-communicative demonstration in which the human retrieved a tennis ball from under an opaque container while manipulating another distant and obviously empty (transparent) one. Subjects were then allowed to choose either in the presence of the demonstrator or after she left the room. Results showed a significant main effect of the demonstration context (presence or absence of the human’s communicative signals), and we also found some evidence for the response-modifying effect of the presence of the human demonstrator during the dogs’ choice. That is, dogs predominantly chose the baited container, but if the demonstration context was communicative and the human was present during the dogs’ choice, subjects’ tendency to select the baited container has been reduced. In agreement with the studies showing sensitivity to human’s communicative signals in dogs, these findings point to a special form of social influence in observational learning situations when it comes to learning about causally opaque and less efficient (compared to what comes natural to the dog) action demonstrations

Design and Optimization of Nanostructured Lipid Carrier Containing Dexamethasone for Ophthalmic Use

The aim of this study was to perform a preformulation study of dexamethasone (DXM)-loaded nanostructured lipid carriers (NLCs) for ocular use. Lipid screening was applied to find the most suitable solid and liquid lipids and surfactant for the NLC formulation. The visual observation was proved with XRD measurements for the establishment of the soluble state of DXM. Thermoanalytical measurements indicated that the most relevant depression of the crystallinity index could be ensured when using a 7:3 solid lipid:oil ratio. In order to optimize the NLC composition, a 23 full factorial experimental design was used. It was established that each independent factor (lipid, DXM, and surfactant concentration) had a significant effect on the particle size while in the case of entrapment efficiency, the DXM and surfactant concentrations were significant. Lower surfactant and lipid concentrations could be beneficial because the stability and the entrapment efficacy of NLCs were more favorable. The toxicity tests on human cornea cells indicated good ophthalmic tolerability of NLCs. The in vitro drug release study predicted a higher concentration of the solute DXM on the eye surface while the Raman mapping penetration study on the porcine cornea showed a high concentration of nanocarriers in the hydrophylic stroma layer

Dog breed differences in visual communication with humans

Domestic dogs (Canis familiaris) have developed a close relationship with humans through the process of domestication. In human-dog interactions, eye contact is a key element of relationship initiation and maintenance. Previous studies have suggested that canine ability to produce human-directed communicative signals is influenced by domestication history, from wolves to dogs, as well as by recent breed selection for particular working purposes. To test the genetic basis for such abilities in purebred dogs, we examined gazing behavior towards humans using two types of behavioral experiments: the `visual contact task' and the `unsolvable task'. A total of 125 dogs participated in the study. Based on the genetic relatedness among breeds subjects were classified into five breed groups: Ancient, Herding, Hunting, Retriever-Mastiff and Working). We found that it took longer time for Ancient breeds to make an eye-contact with humans, and that they gazed at humans for shorter periods of time than any other breed group in the unsolvable situation. Our findings suggest that spontaneous gaze behavior towards humans is associated with genetic similarity to wolves rather than with recent selective pressure to create particular working breeds

Reading faces: differential lateral gaze bias in processing canine and human facial expressions in dogs and 4-year-old children

Sensitivity to the emotions of others provides clear biological advantages. However, in the case of heterospecific relationships, such as that existing between dogs and humans, there are additional challenges since some elements of the expression of emotions are species-specific. Given that faces provide important visual cues for communicating emotional state in both humans and dogs, and that processing of emotions is subject to brain lateralisation, we investigated lateral gaze bias in adult dogs when presented with pictures of expressive human and dog faces. Our analysis revealed clear differences in laterality of eye movements in dogs towards conspecific faces according to the emotional valence of the expressions. Differences were also found towards human faces, but to a lesser extent. For comparative purpose, a similar experiment was also run with 4-year-old children and it was observed that they showed differential processing of facial expressions compared to dogs, suggesting a species-dependent engagement of the right or left hemisphere in processing emotions

New results on the 8Be anomaly

Recently, we observed anomalous internal pair creation for the M1 transition depopulating the 18.15 MeV isoscalar 1$^+$ state in $^8$Be. We observed a significant (σ = 7.37) peak-like deviation from the predicted angular correlation of the e+ e pairs at θ = 140°. To the best of our knowledge no nuclear physics related description of such deviation can be made. However, the deviation can be described by assuming the creation and subsequent decay of a boson with mass of ≈17 MeV. In order to clarify the interpretation, we re-investigated the $^8$Be anomaly with an improved, and independent setup. We have confirmed the signal of the assumed X(17) particle and constrained its mass (m$_0$c $^2$ = 17.01(16) MeV) and branching ratio compared to the γ-decay (B$_x$ = 6(1) × 10$^{−6}$)