EXAMINING THE VALIDITY OF THE LIFE HISTORY CALENDAR

This study examined validity of the Life History Calendar by comparing retrospective and prospective reports of adolescent substance use. Agreement was calculated using kappa and phi coefficients for dichotomous variables, and Bivariate correlations for average substance use. Effects of potential personality, psychopathology, and demographic moderators on agreement were assessed through hierarchical regression analyses and curvilinear relations determined. Results reflected moderate agreement between retrospective and prospective reports of substance use, moderated by personality and psychopathology variables, particularly Agreeableness, symptoms of antisocial personality disorder, and symptoms of substance abuse. Agreement between retrospective and prospective reports was adequate for reports of alcohol and marijuana use for at least six years after initial reports of use. Agreement for cigarette reports was adequate a year after initial reporting

A neutron scattering study of the interplay between structure and magnetism in Ba(Fe1−x_{1-x}Cox_{x})2_2As2_2

Single crystal neutron diffraction is used to investigate the magnetic and structural phase diagram of the electron doped superconductor Ba(Fe$_{1-x}$Co$_x$)$_2$As$_2$. Heat capacity and resistivity measurements have demonstrated that Co doping this system splits the combined antiferromagnetic and structural transition present in BaFe$_2$As$_2$ into two distinct transitions. For $x$=0.025, we find that the upper transition is between the high-temperature tetragonal and low-temperature orthorhombic structures with ($T_{\mathrm{TO}}=99 \pm 0.5$ K) and the antiferromagnetic transition occurs at $T_{\mathrm{AF}}=93 \pm 0.5$ K. We find that doping rapidly suppresses the antiferromagnetism, with antiferromagnetic order disappearing at $x \approx 0.055$. However, there is a region of co-existence of antiferromagnetism and superconductivity. The effect of the antiferromagnetic transition can be seen in the temperature dependence of the structural Bragg peaks from both neutron scattering and x-ray diffraction. We infer from this that there is strong coupling between the antiferromagnetism and the crystal lattice

Revealing invisible brews: a new approach to the chemical identification of ancient beer

While ancient Near Eastern cuneiform texts and iconography unambiguously demonstrate the social, economic, and ritual significance of beer, direct archaeological evidence for beer production or consumption remains surprisingly rare. This scarcity of material evidence renders it difficult to extrapolate information about the ingredients and production processes of beer, on the one hand, and the paraphernalia and social contexts of its consumption, on the other. In recent decades, organic residue analysis has become an essential tool in the identification of ancient alcoholic beverages, but research on Near Eastern beer has focused largely on production and storage vessels, whose form, archaeological context, and associated macroscopic residues already indicated their use in beer production. In this paper, we present a novel field sampling protocol that prevents contamination along with a refined organic residue analysis methodology that relies on a series of co-occurring compounds to identify confidently beer in ceramic vessels. The same compounds were identified in several modern beer samples and, thus, support our identification of a similar fermented barley-based beverage in archaeological samples from the late second millennium BCE site of Khani Masi in northeastern Iraq. The results presented in this paper allow us, for the first time, to unambiguously link a diverse range of vessel types to the consumption and production of beer, identify a fundamental change in Mesopotamian consumption practices, and shed light on the cultural dimensions of Babylonia's encounter with the Zagros-Mesopotamian borderlands

Dependence of Crystallite Formation and Preferential Backbone Orientations on the Side Chain Pattern in PBDTTPD Polymers

Alkyl substituents appended to the π-conjugated main chain account for the solution-processability and film-forming properties of most π-conjugated polymers for organic electronic device applications, including field-effect transistors (FETs) and bulk-heterojunction (BHJ) solar cells. Beyond film-forming properties, recent work has emphasized the determining role that side-chain substituents play on polymer self-assembly and thin-film nanostructural order, and, in turn, on device performance. However, the factors that determine polymer crystallite orientation in thin-films, implying preferential backbone orientation relative to the device substrate, are a matter of some debate, and these structural changes remain difficult to anticipate. In this report, we show how systematic changes in the side-chain pattern of poly(benzo[1,2-b:4,5-b′]dithiophene–alt–thieno[3,4-c]pyrrole-4,6-dione) (PBDTTPD) polymers can (i) influence the propensity of the polymer to order in the π-stacking direction, and (ii) direct the preferential orientation of the polymer crystallites in thin films (e.g., “face-on” vs “edge-on”). Oriented crystallites, specifically crystallites that are well-ordered in the π-stacking direction, are believed to be a key contributor to improved thin-film device performance in both FETs and BHJ solar cells

Size-Dependent Lattice Structure and Confinement Properties in CsPbI₃ Perovskite Nanocrystals: Negative Surface Energy for Stabilization

CsPbI₃ nanocrystals with narrow size distributions were prepared to study the size-dependent properties. The nanocrystals adopt the perovskite (over the nonperovskite orthorhombic) structure with improved stability over thin-film materials. Among the perovskite phases (cubic α, tetragonal β, and orthorhombic γ), the samples are characterized by the γ phase, rather than α, but may have a size-dependent average tilting between adjacent octahedra. Size-dependent lattice constants systematically vary 3% across the size range, with unit cell volume increasing linearly with the inverse of size to 2.1% for the smallest size. We estimate the surface energy to be from −3.0 to −5.1 eV nm⁻² for ligated CsPbI₃ nanocrystals. Moreover, the size-dependent bandgap is best described using a nonparabolic intermediate confinement model. We experimentally determine the bulk bandgap, effective mass, and exciton binding energy, concluding with variations from the bulk α-phase values. This provides a robust route to understanding γ-phase properties of CsPbI₃

Increased pCO2 changes the lipid production in important aquacultural feedstock algae Isochrysis galbana, but not in Tetraselmis suecica

Increased anthropogenic CO2 emissions are leading to an increase in CO2 uptake by the world's oceans and seas, resulting in ocean acidification with a decrease in global ocean water pH by as much as 0.3–0.4 units by the year 2100. The direct effects of changing pCO2 on important microalgal feedstocks are not as well understood. Few studies have focused on lipid composition changes in specific algal species in response to ocean acidification and yet microalgae are an indispensable food source for various marine species, including juvenile shellfish. Isochrysis galbana and Tetraselmis suecica are widely used in aquaculture as feeds for mussels and other shellfish. The total lipid contents and concentrations of I. galbana and T. suecica were investigated when grown under present day (400 ppm) and ocean acidification conditions (1000 ppm) to elucidate the impact of increasing pCO2 on an important algae feedstock. Total lipids, long-chain alkenones (LCAs) and alkenoates decreased at 1000 ppm in I. galbana. I. galbana produces higher lipids than T. suecica, and is perhaps as a result more impacted by the change in carbon available for lipid production under higher pCO2. I. galbana is an important feedstock, more easily assimilated for growth in juvenile shellfish and reductions in lipid composition may prove problematic for the growth of future shellfish aquaculture. Our findings suggest that higher pCO2 impacts on algal lipid growth are species specific and warrant further study. It is therefore vital to examine the impact of high CO2 on algal lipid production, especially those commercial shellfish feed varieties to predict future impacts on commercial aquaculture