Emotional Intelligence as a Credible Psychological Construct: Real but Elusive – A Conceptual Interpretation of Meta-Analytic Investigation Outcomes

ABSTRACT Emotional intelligence was thought to fill a gap that otherwise could not be explained by less encumbered traditional intelligence measures, and hence, its almost immediate popularity and appeal. The research, however, has been rather equivocal and suffers from poor operational definitions of the dependent variables and limited external validity. The results of a recent meta-analysis (Joseph, et al., 2014) demonstrated that the mixed EI measures overwhelmingly overlapped with traditional psychological constructs including: Ability EI, Self-Efficacy, Self-rated Performance, Conscientiousness, Emotional Stability, Extraversion, and General Mental Ability. The apparent inconsistency of the relative predictive utility of disparate measures of EI   does not preclude its consideration as a heuristic explanatory construct in organizational leadership and industrial-organizational psychology. It is reasonable to maintain that a unique predictive combination of previously known variables may still constitute a viable new construct – such as EI. Emotional Intelligence represents a heuristic explanatory device that makes a positive contribution to our understanding of organizational development and leadership behavior. Emotional intelligence, for all its ambiguity and measurement challenges, still represents a viable construct in leadership theory and organizational development. EI does much to explain why certain individuals are more effective than others in business and in life. The mere fact that the various components of EI can be predicted by more discrete and traditional measures in no way serves to diminish or undermine the utility and integrity of the concept. Keywords: emotional intelligence, leadership theory, organizational development, meta-analysis, copyrights & patents, psychological constructs

On the resistivity at low temperatures in electron-doped cuprate superconductors

We measured the magnetoresistance as a function of temperature down to 20mK and magnetic field for a set of underdoped PrCeCuO (x=0.12) thin films with controlled oxygen content. This allows us to access the edge of the superconducting dome on the underdoped side. The sheet resistance increases with increasing oxygen content whereas the superconducting transition temperature is steadily decreasing down to zero. Upon applying various magnetic fields to suppress superconductivity we found that the sheet resistance increases when the temperature is lowered. It saturates at very low temperatures. These results, along with the magnetoresistance, cannot be described in the context of zero temperature two dimensional superconductor-to-insulator transition nor as a simple Kondo effect due to scattering off spins in the copper-oxide planes. We conjecture that due to the proximity to an antiferromagnetic phase magnetic droplets are induced. This results in negative magnetoresistance and in an upturn in the resistivity.Comment: Accepted in Phys. Rev.

Immunoglobulin signal transduction guides the specificity of B cell-T cell interactions and is blocked in tolerant self-reactive B cells.

The specificity of antibody (Ab) responses depends on focusing helper T (Th) lymphocyte signals to suitable B lymphocytes capable of binding foreign antigens (Ags), and away from nonspecific or self-reactive B cells. To investigate the molecular mechanisms that prevent the activation of self-reactive B lymphocytes, the activation requirements of B cells specific for the Ag hen egg lysozyme (HEL) obtained from immunoglobulin (Ig)-transgenic mice were compared with those of functionally tolerant B cells isolated from Ig-transgenic mice which also express soluble HEL. To eliminate the need for surface (s)Ig-mediated Ag uptake and presentation and allow the effects of sIg signaling to be studied in isolation, we assessed the ability of allogeneic T cells from bm12 strain mice to provide in vivo help to C57BL/6 strain-transgenic B cells. Interestingly, non-tolerant Ig-transgenic B cells required both allogeneic Th cells and binding of soluble HEL for efficient activation and Ab production. By contrast, tolerant self-reactive B cells from Ig/HEL double transgenic mice responded poorly to the same combination of allogeneic T cells and soluble HEL. The tolerant B cells were nevertheless normally responsive to stimulation with interleukin 4 and anti-CD40 Abs in vitro, suggesting that they retained the capacity to respond to mediators of T cell help. However, the tolerant B cells exhibited a proximal block in the sIg signaling pathway which prevented activation of receptor-associated tyrosine kinases in response to the binding of soluble HEL. The functional significance of this sIg signaling defect was confirmed by using a more potent membrane-bound form of HEL capable of triggering sIg signaling in tolerant B cells, which markedly restored their ability to collaborate with allogeneic Th cells and produce Ab. These findings indicate that Ag-specific B cells require two signals for mounting a T cell-dependent Ab response and identify regulation of sIg signaling as a mechanism for controlling self-reactive B cells

γδ T cells affect IL-4 production and B-cell tolerance

γδ T cells can influence specific antibody responses. Here, we report that mice deficient in individual γδ T-cell subsets have altered levels of serum antibodies, including all major subclasses, sometimes regardless of the presence of αβ T cells. One strain with a partial γδ deficiency that increases IgE antibodies also displayed increases in IL-4–producing T cells (both residual γδ T cells and αβ T cells) and in systemic IL-4 levels. Its B cells expressed IL-4–regulated inhibitory receptors (CD5, CD22, and CD32) at diminished levels, whereas IL-4–inducible IL-4 receptor α and MHCII were increased. They also showed signs of activation and spontaneously formed germinal centers. These mice displayed IgE-dependent features found in hyper-IgE syndrome and developed antichromatin, antinuclear, and anticytoplasmic autoantibodies. In contrast, mice deficient in all γδ T cells had nearly unchanged Ig levels and did not develop autoantibodies. Removing IL-4 abrogated the increases in IgE, antichromatin antibodies, and autoantibodies in the partially γδ-deficient mice. Our data suggest that γδ T cells, controlled by their own cross-talk, affect IL-4 production, B-cell activation, and B-cell tolerance

Lenticular galaxies with UV-rings

By using the public UV imaging data obtained by the GALEX (Galaxy Ultraviolet Explorer) for nearby galaxies, we have compiled a list of lenticular galaxies possessing ultraviolet rings - starforming regions tightly confined to particular radial distances from galactic centers. We have studied large-scale structure of these galaxies in the optical bands by using the data of the SDSS (Sloan Digital Sky Survey): we have decomposed the galactic images into large-scale disks and bulges, have measured the ring optical colours from the residual images after subtracting model disks and bulges, and have compared the sizes of the rings in the optical light and in the UV-band. The probable origin of the outer starforming ring appearances in unbarred galaxies demonstrating otherwise the regular structure and homogeneously old stellar population beyond the rings is discussed.Comment: 9 pages plus one big colour figure in the Appendix; the slightly expanded version of the paper accepted to Astronomy Letter

Canalization of the evolutionary trajectory of the human influenza virus

Since its emergence in 1968, influenza A (H3N2) has evolved extensively in genotype and antigenic phenotype. Antigenic evolution occurs in the context of a two-dimensional 'antigenic map', while genetic evolution shows a characteristic ladder-like genealogical tree. Here, we use a large-scale individual-based model to show that evolution in a Euclidean antigenic space provides a remarkable correspondence between model behavior and the epidemiological, antigenic, genealogical and geographic patterns observed in influenza virus. We find that evolution away from existing human immunity results in rapid population turnover in the influenza virus and that this population turnover occurs primarily along a single antigenic axis. Thus, selective dynamics induce a canalized evolutionary trajectory, in which the evolutionary fate of the influenza population is surprisingly repeatable and hence, in theory, predictable.Comment: 29 pages, 5 figures, 10 supporting figure

Basophils Produce IL-4 and Accumulate in Tissues after Infection with a Th2-inducing Parasite

Using mice in which the eGfp gene replaced the first exon of the Il4 gene (G4 mice), we examined production of interleukin (IL)-4 during infection by the intestinal nematode Nippostrongylus brasiliensis (Nb). Nb infection induced green fluorescent protein (GFP)pos cells that were FcɛRIpos, CD49bbright, c-kitneg, and Gr1neg. These cells had lobulated nuclei and granules characteristic of basophils. They were found mainly in the liver and lung, to a lesser degree in the spleen, but not in the lymph nodes. Although some liver basophils from naive mice express GFP, Nb infection enhanced GFP expression and increased the number of tissue basophils. Similar basophil GFP expression was found in infected Stat6−/− mice. Basophils did not increase in number in infected Rag2−/− mice; Rag2−/− mice reconstituted with CD4 T cells allowed significant basophil accumulation, indicating that CD4 T cells can direct both tissue migration of basophils and enhanced IL-4 production. IL-4 production was immunoglobulin independent and only partially dependent on IL-3. Thus, infection with a parasite that induces a “Th2-type response” resulted in accumulation of tissue basophils, and these cells, stimulated by a non-FcR cross-linking mechanism, are a principal source of in vivo IL-4 production

Two formation channels of UCDs in Hickson Compact Groups

The formation of ultra-compact dwarf galaxies (UCDs) is believed to be interaction driven, and UCDs are abundant in the cores of galaxy clusters, environments that mark the end-point of galaxy evolution. Nothing is known about the properties of UCDs in compact groups of galaxies, environments where most of galaxy evolution and interaction is believed to occur and where UCDs in intermediate state of evolution may be expected. The main goal of this study is to detect and characterize, for the first time, the UCD population of compact groups. For that, 2 groups in different evolutionary stages, HCG 22 and HCG 90, were targeted with VLT/FORS2/MXU. We detect 16 and 5 objects belonging to HCG 22 and HCG 90, respectively, covering the magnitude range -10.0 > M_R > -11.5 mag. Their colours are consistent with old ages covering a broad range in metallicities. Photometric mass estimates put 4 objects in HCG 90 and 9 in HCG 22 in the mass range of UCDs (>2x10^6 M_Sun) for an assumed age of 12 Gyr. These UCDs are on average 2-3 times larger than typical Galactic GCs, covering a range of 2 >~ r_h >~ 21 pc. The UCDs in HCG 22 are more concentrated around the central galaxy than in HCG 90, at the 99% confidence level. They cover a broad range in [alpha/Fe] abundances from sub- to super-solar. The spectra of 3 UCDs show tentative evidence for intermediate age stellar populations. We calculate the specific frequency (S_N) of UCDs for both groups, finding that HCG 22 has about three times higher S_N than HCG 90. The ensemble properties of the detected UCDs supports 2 co-existing formation channels: a star cluster origin and an origin as tidally stripped dwarf nuclei. Our results imply that the UCDs detected in both groups do not, in their majority, originate from relatively recent galaxy interactions. Most of the detected UCDs have likely been brought into the group with their host galaxies.[abridged]Comment: Accepted for publication at A&A, 17 pages, 9 figures + 2 additional figure