			Home About us Contact

Structure Result (structure + result)

Distribution by Scientific Domains

Life Sciences	50%

Selected Abstracts

Pre-Hispanic Mesoamerican demography approximates the present-day ancestry of Mestizos throughout the territory of Mexico

AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 3 2009
Rodrigo Rubi-Castellanos
Abstract Over the last 500 years, admixture among Amerindians, Europeans, and Africans, principally, has come to shape the present-day gene pool of Mexicans, particularly Mestizos, who represent about 93% of the total Mexican population. In this work, we analyze the genetic data of 13 combined DNA index system-short tandem repeats (CODIS-STRs) in 1,984 unrelated Mestizos representing 10 population samples from different regions of Mexico, namely North, West, Central, and Southeast. The analysis of molecular variance (AMOVA) test demonstrated low but significant differentiation among Mestizos from different regions (FST = 0.34%; P = 0.0000). Although the spatial analysis of molecular variance (SAMOVA) predicted clustering Mestizo populations into four well-delimited groups, the main differentiation was observed between Northwest when compared with Central and Southeast regions. In addition, we included analysis of individuals of Amerindian (Purepechas), European (Huelva, Spain), and African (Fang) origin. Thus, STRUCTURE analysis was performed identifying three well-differentiated ancestral populations (k = 3). STRUCTURE results and admixture estimations by means of LEADMIX software in Mestizo populations demonstrated genetic heterogeneity or asymmetric admixture throughout Mexico, displaying an increasing North-to-South gradient of Amerindian ancestry, and vice versa regarding the European component. Interestingly, this distribution of Amerindian ancestry roughly reflects pre-Hispanic Native-population density, particularly toward the Mesoamerican area. The forensic, epidemiological, and evolutionary implications of these findings are discussed herein. Am J Phys Anthropol 2009. © 2009 Wiley-Liss, Inc. [source]

Effects of Structural Variation on the Photocatalytic Performance of Hydrothermally Synthesized BiVO4,

ADVANCED FUNCTIONAL MATERIALS, Issue 16 2006
J. Yu
Abstract Highly crystalline monoclinic scheelite BiVO4 powders are synthesized from aqueous Bi(NO3)3 and NH4VO3 solutions over a wide range of pH by a hydrothermal process. BiVO4 powders with various morphologies, surface textures, and grain shapes are selectively synthesized by adjusting the pH. The dependence of the Raman peak position and intensity on the synthesis conditions indicates that the symmetry distortions in the local structure of the synthesized BiVO4 are affected by the preparation conditions. These variations in the local structure result in the modification of the electronic structure of BiVO4, which results in a blue-shift in the UV-vis absorption spectrum of hydrothermally synthesized BiVO4 in comparison with a well-crystallized sample prepared by homogeneous coprecipitation. The photocatalytic activities for O2 evolution from an aqueous AgNO3 solution under visible-light irradiation are strongly dependent on the pH used in the synthesis. The differences in the photocatalytic activities between BiVO4 samples prepared under various conditions is attributed to the degree of structural distortion, leading to differences in the mobility of photogenerated holes formed in the valence band, which consists of Bi,6s and O,2p orbitals. [source]

Long-term changes in the trophic level of the Celtic Sea fish community and fish market price distribution

JOURNAL OF APPLIED ECOLOGY, Issue 3 2002
J. K. Pinnegar
Summary 1The intensive exploitation of fish communities often leads to substantial reductions in the abundance of target species, with ramifications for the structure and stability of the ecosystem as a whole. 2We explored changes in the mean trophic level of the Celtic Sea (ICES divisions VII f,j) fish community using commercial landings, survey data and estimates of trophic level derived from the analysis of nitrogen stable isotopes. 3Our analyses showed that there has been a significant decline in the mean trophic level of survey catches from 1982 to 2000 and a decline in the trophic level of landings from 1946 to 1998. 4The decline in mean trophic level through time resulted from a reduction in the abundance of large piscivorous fishes and an increase in smaller pelagic species which feed at a lower trophic level. 5Similar patterns of decline in the trophic level of both catches and landings imply that there have been substantial changes in the underlying structure of the Celtic Sea fish community and not simply a change in fishery preferences. 6We suggest that the reported changes in trophic structure result from reductions in the spawning stock biomass of traditional target species associated with intensive fishing, together with long-term climate variability. 7The relative distribution of fish market prices has changed significantly over the past 22 years, with high trophic level species experiencing greater price rises than lower trophic level species. 8Although decreased abundance of high trophic level species will ultimately have negative economic consequences, the reduction in mean trophic level of the fish community as a whole may allow the system to sustain higher fishery yields. 9Management objectives in this fishery will depend on the relative values that society attaches to economic profit and protein production. [source]

Self-Assembly, Structure and Solution Dynamics of Tetranuclear Zn2+ Hydrazone [2×2] Grid-Type Complexes

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 4 2006
Mihail Barboiu
Abstract We describe the self-assembly processes as well as the structural and physico-chemical properties of [2×2]Zn2+4 grid complexes involving the bis-tridentate ligands 7,12, based on bis(hydrazone)pyrimidine complexation subunits and octahedrally coordinated Zn2+ ions. The NMR spectroscopic data and the X-ray crystal structure results indicate that in solution and in the solid state the complexes 13,18 adopt a very compact arrangement providing stable [2×2] hydrazone-grid arrays. The ,,, stacking between the phenyl ring and the hydrazone units of the perpendicular ligands in the complexes induces a perfect orthogonal arrangement suitable for applications in self-organized metallosupramolecular systems. Zinc complexes provide an opportunity to study the acid,base chemistry without the added effects due to paramagnetism or redox chemistry. The intermediate protonated grids undergo relatively rapid proton exchange on the NMR timescale, the presence of a sharp pyrimidine proton resonance suggesting that there is significant delocalization of the negative charge along the backbone of the ligand. Rotation of the phenyl ring is observed. It involves probably a mechanism in which one of the ligands partially dissociates allowing the initially intercalated phenyl group to rotate, before recoordination of the terminal pyridine. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source]